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The Project Gutenberg eBook of The Microscope. Its History,
Construction, and Application 15th ed.
This eBook is for the use of anyone anywhere in the United States and
most other parts of the world at no cost and with almost no restrictions
whatsoever. You may copy it, give it away or re-use it under the terms
of the Project Gutenberg License included with this eBook or online at
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will have to check the laws of the country where you are located
before using this eBook.
Title: The Microscope. Its History, Construction, and Application 15th
ed.
Author: Jabez Hogg
Release date: January 25, 2020 [eBook #61233]
Most recently updated: October 17, 2024
Language: English
Other information and formats: www.gutenberg.org/ebooks/61233
Credits: Produced by Wayne Hammond, Chris Curnow, and the PGDP
volunteers.
*** START OF THE PROJECT GUTENBERG EBOOK THE
MICROSCOPE. ITS HISTORY, CONSTRUCTION, AND APPLICATION
15TH ED. ***
Construction, and Application 15th ed.
This eBook is for the use of anyone anywhere in the United States and
most other parts of the world at no cost and with almost no restrictions
whatsoever. You may copy it, give it away or re-use it under the terms
of the Project Gutenberg License included with this eBook or online at
www.gutenberg.org. If you are not located in the United States, you
will have to check the laws of the country where you are located
before using this eBook.
Title: The Microscope. Its History, Construction, and Application 15th
ed.
Author: Jabez Hogg
Release date: January 25, 2020 [eBook #61233]
Most recently updated: October 17, 2024
Language: English
Other information and formats: www.gutenberg.org/ebooks/61233
Credits: Produced by Wayne Hammond, Chris Curnow, and the PGDP
volunteers.
*** START OF THE PROJECT GUTENBERG EBOOK THE
MICROSCOPE. ITS HISTORY, CONSTRUCTION, AND APPLICATION
15TH ED. ***
Page 4
RADIOLARIA.
Page 5
THE
MICROSCOPE
ITS HISTORY, CONSTRUCTION, AND APPLICATION
BEING A FAMILIAR INTRODUCTION TO THE USE OF
THE INSTRUMENT, AND THE STUDY OF
MICROSCOPICAL SCIENCE
By JABEZ HOGG, M.R.C.S., F.R.M.S.,
FORMERLY AND FOR TWENTY-FIVE YEARS SURGEON TO THE ROYAL WESTMINSTER
OPHTHALMIC
HOSPITAL; PAST PRESIDENT OF THE MEDICAL MICROSCOPICAL SOCIETY; HONORARY
FELLOW OF THE ACADEMY OF SCIENCES, PHILADELPHIA; OF THE MEDICO-LEGAL
SOCIETY, NEW YORK; OF THE BELGIAN MICROSCOPICAL SOCIETY, ETC.; AUTHOR
OF “ELEMENTS OF NATURAL PHILOSOPHY,” “A MANUAL OF
OPHTHALMOSCOPIC SURGERY,” ETC.
MICROSCOPE
ITS HISTORY, CONSTRUCTION, AND APPLICATION
BEING A FAMILIAR INTRODUCTION TO THE USE OF
THE INSTRUMENT, AND THE STUDY OF
MICROSCOPICAL SCIENCE
By JABEZ HOGG, M.R.C.S., F.R.M.S.,
FORMERLY AND FOR TWENTY-FIVE YEARS SURGEON TO THE ROYAL WESTMINSTER
OPHTHALMIC
HOSPITAL; PAST PRESIDENT OF THE MEDICAL MICROSCOPICAL SOCIETY; HONORARY
FELLOW OF THE ACADEMY OF SCIENCES, PHILADELPHIA; OF THE MEDICO-LEGAL
SOCIETY, NEW YORK; OF THE BELGIAN MICROSCOPICAL SOCIETY, ETC.; AUTHOR
OF “ELEMENTS OF NATURAL PHILOSOPHY,” “A MANUAL OF
OPHTHALMOSCOPIC SURGERY,” ETC.
Page 6
WITH UPWARDS OF
NINE HUNDRED
ENGRAVED FIFTEENTH EDITION
AND COLOURED RE-CONSTRUCTED,
ILLUSTRATIONS BY RE-WRITTEN,
TUFFEN WEST REVISED, AND
AND An 18th Century ENLARGED
OTHER ARTISTS Microscope. THROUGHOUT
LONDON AND NEW YORK
GEORGE ROUTLEDGE & SONS, LIMITED
1898
BRADBURY, AGNEW, & CO. I.D., PRINTERS,
LONDON AND TONBRIDGE.
NINE HUNDRED
ENGRAVED FIFTEENTH EDITION
AND COLOURED RE-CONSTRUCTED,
ILLUSTRATIONS BY RE-WRITTEN,
TUFFEN WEST REVISED, AND
AND An 18th Century ENLARGED
OTHER ARTISTS Microscope. THROUGHOUT
LONDON AND NEW YORK
GEORGE ROUTLEDGE & SONS, LIMITED
1898
BRADBURY, AGNEW, & CO. I.D., PRINTERS,
LONDON AND TONBRIDGE.
Page 7
PREFACE TO THE FIFTEENTH EDITION.
T HE First Edition of this work appeared in 1854, a time in the history of
the Microscope when the instrument, as an aid to original scientific
research, may be said to have been in its infancy. Then certainly it was
seldom employed in the laboratory or the medical schools. Now, however,
as I anticipated, it has asserted its proper position, and has at length become
one of the most important auxiliaries to science, and a direct incentive to
original work, while it has doubtless exercised considerable influence over
the student’s power of observation, and materially assisted in his studies, let
his ultimate object and pursuits be what they may.
The greater use made of the Microscope has likewise conferred benefits of
untold value upon the arts and industries of the country, thereby adding to
the national prosperity in ways as manifold as unique. The Microscope has
also proved of immense value in the promotion of the health of the
community, and the art and science of healing, since the theory of medicine
has become a science, resting on the minute microscopical examination of
animal tissues.
The work of research in the sister sciences and by other methods has,
during the last decade, received a corresponding impetus, while it has
undoubtedly tended towards elaboration and specialisation in all
departments. In consequence, the progress of microscopical science has
become more dependent upon the specialist for gaining accurate knowledge
and for certain important details seen to be branching out in many
directions. There never was a time when the instrument was so constantly
and generally resorted to and with so much confidence and advantage, as
the present. It has shown itself equal to the task imposed—that of teaching
the eye to see things that are new, and also, what is perhaps of more
importance, to perceive things which had been entirely overlooked. The
older defects, perhaps, arose from two causes; the want of more careful
training of the organ of vision, and the want of sufficient power and
T HE First Edition of this work appeared in 1854, a time in the history of
the Microscope when the instrument, as an aid to original scientific
research, may be said to have been in its infancy. Then certainly it was
seldom employed in the laboratory or the medical schools. Now, however,
as I anticipated, it has asserted its proper position, and has at length become
one of the most important auxiliaries to science, and a direct incentive to
original work, while it has doubtless exercised considerable influence over
the student’s power of observation, and materially assisted in his studies, let
his ultimate object and pursuits be what they may.
The greater use made of the Microscope has likewise conferred benefits of
untold value upon the arts and industries of the country, thereby adding to
the national prosperity in ways as manifold as unique. The Microscope has
also proved of immense value in the promotion of the health of the
community, and the art and science of healing, since the theory of medicine
has become a science, resting on the minute microscopical examination of
animal tissues.
The work of research in the sister sciences and by other methods has,
during the last decade, received a corresponding impetus, while it has
undoubtedly tended towards elaboration and specialisation in all
departments. In consequence, the progress of microscopical science has
become more dependent upon the specialist for gaining accurate knowledge
and for certain important details seen to be branching out in many
directions. There never was a time when the instrument was so constantly
and generally resorted to and with so much confidence and advantage, as
the present. It has shown itself equal to the task imposed—that of teaching
the eye to see things that are new, and also, what is perhaps of more
importance, to perceive things which had been entirely overlooked. The
older defects, perhaps, arose from two causes; the want of more careful
training of the organ of vision, and the want of sufficient power and
Page 8
precision in the optical part of the Microscope itself. Both of these obstacles
have been to a considerable extent removed, and all educational systems are
looked upon as incomplete without a knowledge of the Microscope.
A step has already been taken in another direction, that of furnishing special
forms of instruments, better adapted to the uses to which they will hereafter
be put, and purposely designed for chemical and analytical processes, for
petrological pursuits, the geometrical measurement of crystals, for special
work in connection with manufacturing industries, for the dairyman, and
the farmer. For the detection of adulterations—that of butter, for example—
a newer form of instrument has been devised, namely, a “Butro-
refractometer,” by the help of which any adulteration of this universal
article of diet will at once be revealed. The form of instrument upon which
the optician has expended a greater amount of skill than perhaps on any
other is the Bacteriological Microscope, as may be inferred from the larger
space I have devoted to this important adjunct, since by original research,
there can be no doubt a still greater future is in store for science in this
special department of microscopy. But perfect success in this direction
remains very much with the practical optician, and the further
improvements made in the optical part of the instrument, since it is admitted
that the highest theoretical perfection has not yet been reached.
It is a commonplace remark that every question solved is a step towards
new problems waiting solution. It is equally obvious that many difficulties
must be encountered by every author who uses his best endeavours to
supply a standard volume or even a fairly comprehensive text-book on the
Microscope, one that will remain a sure guide for any lengthened period.
Such a success I regard as scarcely possible. I may, however, notice that my
earlier work has met with a great amount of appreciation, and its utility
acknowledged in the past by a demand almost unprecedented, edition after
edition being called for.
It is hardly necessary to add that my task has been accomplished with an
earnest desire to assist in diffusing a love for an instrument which has been
my constant companion for upwards of sixty years.1 Moreover, I have a
firm conviction of the real utility of the Microscope in the work of
education, its practical value in many branches of science, art, and
have been to a considerable extent removed, and all educational systems are
looked upon as incomplete without a knowledge of the Microscope.
A step has already been taken in another direction, that of furnishing special
forms of instruments, better adapted to the uses to which they will hereafter
be put, and purposely designed for chemical and analytical processes, for
petrological pursuits, the geometrical measurement of crystals, for special
work in connection with manufacturing industries, for the dairyman, and
the farmer. For the detection of adulterations—that of butter, for example—
a newer form of instrument has been devised, namely, a “Butro-
refractometer,” by the help of which any adulteration of this universal
article of diet will at once be revealed. The form of instrument upon which
the optician has expended a greater amount of skill than perhaps on any
other is the Bacteriological Microscope, as may be inferred from the larger
space I have devoted to this important adjunct, since by original research,
there can be no doubt a still greater future is in store for science in this
special department of microscopy. But perfect success in this direction
remains very much with the practical optician, and the further
improvements made in the optical part of the instrument, since it is admitted
that the highest theoretical perfection has not yet been reached.
It is a commonplace remark that every question solved is a step towards
new problems waiting solution. It is equally obvious that many difficulties
must be encountered by every author who uses his best endeavours to
supply a standard volume or even a fairly comprehensive text-book on the
Microscope, one that will remain a sure guide for any lengthened period.
Such a success I regard as scarcely possible. I may, however, notice that my
earlier work has met with a great amount of appreciation, and its utility
acknowledged in the past by a demand almost unprecedented, edition after
edition being called for.
It is hardly necessary to add that my task has been accomplished with an
earnest desire to assist in diffusing a love for an instrument which has been
my constant companion for upwards of sixty years.1 Moreover, I have a
firm conviction of the real utility of the Microscope in the work of
education, its practical value in many branches of science, art, and
Page 9
manufacturing industries. These are my chief reasons for applying myself
once more to the task of revision, rewriting, and rearranging and bringing
this book as far as possible into line with the knowledge gained in chemical
pathology and bacteriology.
It will be noticed that in the first part, my subjects have as far as possible
been treated from a historical point of view. This method has enabled me to
affix dates of introduction of special inventions and improvements made in
the instrument and its appliances. The enlargement of my pages has enabled
me to devote more space to bacteriological processes, and by the further
addition of plates and several hundred illustrations to more fully elucidate
the subject matter of my text. In an Appendix I have introduced a selection
of “Formulæ and Methods” of staining, mounting, etc., also tables of the
“Metrical System,” now in general use in the laboratory; together with
comparative thermometric values, all of which I trust may prove of service
to the student.
Before bringing these few prefatory remarks to a close, a pleasing duty
devolves upon me—that of tendering my thanks for cordial aid received
from Professor Dr. Edgar Crookshank in dealing with his special subject,
Bacteriology. From his valuable “Text-Book on Bacteriology” I have
extracted much useful matter. I am equally indebted to Professor Marshall
Ward, F.R.S., Cambridge, for much information on “Economic Botany,”
and the great advances made in the knowledge of the uses of plants, and the
industrial value of bacteria in particular. My acknowledgments are also due
to the Messrs. Warne for many illustrations placed at my disposal, and for
useful facts derived from their “Royal Natural History.” It will, however, be
seen that the results of a large amount of independent observation have been
consigned to my pages. As the references show, recourse has been had to
original sources for trustworthy, reliable information on many subjects.
These are constantly, almost daily, being added to, as is made manifest by
the numerous periodical publications of the day devoted to this and kindred
sciences; the foremost and most important among which is that almost
exclusively given to microscopical science, “The Journal of the Royal
Microscopical Society of London,” the perusal of which I commend to my
readers.
once more to the task of revision, rewriting, and rearranging and bringing
this book as far as possible into line with the knowledge gained in chemical
pathology and bacteriology.
It will be noticed that in the first part, my subjects have as far as possible
been treated from a historical point of view. This method has enabled me to
affix dates of introduction of special inventions and improvements made in
the instrument and its appliances. The enlargement of my pages has enabled
me to devote more space to bacteriological processes, and by the further
addition of plates and several hundred illustrations to more fully elucidate
the subject matter of my text. In an Appendix I have introduced a selection
of “Formulæ and Methods” of staining, mounting, etc., also tables of the
“Metrical System,” now in general use in the laboratory; together with
comparative thermometric values, all of which I trust may prove of service
to the student.
Before bringing these few prefatory remarks to a close, a pleasing duty
devolves upon me—that of tendering my thanks for cordial aid received
from Professor Dr. Edgar Crookshank in dealing with his special subject,
Bacteriology. From his valuable “Text-Book on Bacteriology” I have
extracted much useful matter. I am equally indebted to Professor Marshall
Ward, F.R.S., Cambridge, for much information on “Economic Botany,”
and the great advances made in the knowledge of the uses of plants, and the
industrial value of bacteria in particular. My acknowledgments are also due
to the Messrs. Warne for many illustrations placed at my disposal, and for
useful facts derived from their “Royal Natural History.” It will, however, be
seen that the results of a large amount of independent observation have been
consigned to my pages. As the references show, recourse has been had to
original sources for trustworthy, reliable information on many subjects.
These are constantly, almost daily, being added to, as is made manifest by
the numerous periodical publications of the day devoted to this and kindred
sciences; the foremost and most important among which is that almost
exclusively given to microscopical science, “The Journal of the Royal
Microscopical Society of London,” the perusal of which I commend to my
readers.
Page 10
London, July, 1898.
Page 11
PREFACE TO THE FIRST EDITION.
T HE Author of this Publication entered upon his task with some
hesitation and diffidence; but the reasons which influenced him to
undertake it may be briefly told, and they at once explain his motives, and
plead his justification, for the work which he now ventures to submit to the
indulgent consideration of his readers.
It had been to him for some time a subject of regret that one of the most
useful and fascinating studies—that which belongs to the domain of
microscopic observation—should be, if not wholly neglected, at best but
coldly and indifferently appreciated by the great mass of the general public;
and he formed a strong opinion that this apathy and inattention were mainly
attributable to the want of some concise, yet sufficiently comprehensive,
popular account of the Microscope, both as regards the management and
manipulation of the instrument, and the varied wonders and hidden realms
of beauty that are disclosed and developed by its aid. He saw around him
valuable, erudite, and splendid volumes, which, however, being chiefly
designed for circulation amongst a special class of readers, were necessarily
published at a price that renders them practically unattainable by the great
bulk of the public. They are careful and beautiful contributions to the
objects of science, but they do not adequately bring the value and charm of
microscopic studies home, so to speak, to the firesides of the people. Day
after day, new and interesting discoveries, and amplifications of truth
already discerned, have been made, but they have been either sacrificed in
serials, or, more usually, devoted to the pages of class publications; and thus
this most important and attractive study has been, in a great measure, the
province of the few only, who have derived from it a rich store of
enlightenment and gratification: the many not having, however,
participated, to any great extent, in the instruction and entertainment which
always follow in the train of microscopical science.2
T HE Author of this Publication entered upon his task with some
hesitation and diffidence; but the reasons which influenced him to
undertake it may be briefly told, and they at once explain his motives, and
plead his justification, for the work which he now ventures to submit to the
indulgent consideration of his readers.
It had been to him for some time a subject of regret that one of the most
useful and fascinating studies—that which belongs to the domain of
microscopic observation—should be, if not wholly neglected, at best but
coldly and indifferently appreciated by the great mass of the general public;
and he formed a strong opinion that this apathy and inattention were mainly
attributable to the want of some concise, yet sufficiently comprehensive,
popular account of the Microscope, both as regards the management and
manipulation of the instrument, and the varied wonders and hidden realms
of beauty that are disclosed and developed by its aid. He saw around him
valuable, erudite, and splendid volumes, which, however, being chiefly
designed for circulation amongst a special class of readers, were necessarily
published at a price that renders them practically unattainable by the great
bulk of the public. They are careful and beautiful contributions to the
objects of science, but they do not adequately bring the value and charm of
microscopic studies home, so to speak, to the firesides of the people. Day
after day, new and interesting discoveries, and amplifications of truth
already discerned, have been made, but they have been either sacrificed in
serials, or, more usually, devoted to the pages of class publications; and thus
this most important and attractive study has been, in a great measure, the
province of the few only, who have derived from it a rich store of
enlightenment and gratification: the many not having, however,
participated, to any great extent, in the instruction and entertainment which
always follow in the train of microscopical science.2
Page 12
The manifold uses and advantages of the Microscope crowd upon us in
such profusion, that we can only attempt to enumerate them in the briefest
and most rapid manner in these prefatory pages.
It is not many years since this invaluable instrument was regarded in the
light of a costly toy; it is now the inseparable companion of the man of
science. In the medical world, its utility and necessity are fully appreciated,
even by those who formerly were slow to perceive its benefits; now,
knowledge which could not be obtained even by the minutest dissection is
acquired readily by its assistance, which has become as essential to the
anatomist and pathologist as are the scalpel and bedside observation. The
smallest portion of a diseased structure, placed under a Microscope, will tell
more in one minute to the experienced eye than could be ascertained by
long examination of the mass of disease in the ordinary method.
Microscopic agency, in thus assisting the medical man, contributes much to
the alleviation of those multiplied “ills which flesh is heir to.” So fully
impressed were the Council of the Royal College of Surgeons with the
importance of the facts brought to light in a short space of time, that, in
1841, they determined to establish a Professorship of Histology, and to form
a collection of preparations of the elementary tissues of both animals and
vegetables, healthy and morbid, which should illustrate the value of
microscopical investigations in physiology and medical science. From that
time, histological anatomy deservedly became an important branch of the
education of the medical student.
In the study of Vegetable Physiology, the Microscope is an indispensable
instrument; it enables the student to trace the earliest forms of vegetable
life, and the functions of the different tissues in the growth of plants.
Valuable assistance is derived from its agency in the detection of
adulterations. In the examination of flour, an article of so much importance
to all, the Microscope enables us to judge of the size and shape of the
starch-grains, their markings, their isolation and agglomeration, and thus to
distinguish the starch-grains of one meal from those of another. It detects
these and other ingredients, invisible to the naked eye, whether combined in
atoms or aggregated in crystals, which adulterate our food, our drink, and
our medicines. It discloses the lurking poison in the minute crystallisations
which its solutions precipitate. “It tells the murderer that the blood which
such profusion, that we can only attempt to enumerate them in the briefest
and most rapid manner in these prefatory pages.
It is not many years since this invaluable instrument was regarded in the
light of a costly toy; it is now the inseparable companion of the man of
science. In the medical world, its utility and necessity are fully appreciated,
even by those who formerly were slow to perceive its benefits; now,
knowledge which could not be obtained even by the minutest dissection is
acquired readily by its assistance, which has become as essential to the
anatomist and pathologist as are the scalpel and bedside observation. The
smallest portion of a diseased structure, placed under a Microscope, will tell
more in one minute to the experienced eye than could be ascertained by
long examination of the mass of disease in the ordinary method.
Microscopic agency, in thus assisting the medical man, contributes much to
the alleviation of those multiplied “ills which flesh is heir to.” So fully
impressed were the Council of the Royal College of Surgeons with the
importance of the facts brought to light in a short space of time, that, in
1841, they determined to establish a Professorship of Histology, and to form
a collection of preparations of the elementary tissues of both animals and
vegetables, healthy and morbid, which should illustrate the value of
microscopical investigations in physiology and medical science. From that
time, histological anatomy deservedly became an important branch of the
education of the medical student.
In the study of Vegetable Physiology, the Microscope is an indispensable
instrument; it enables the student to trace the earliest forms of vegetable
life, and the functions of the different tissues in the growth of plants.
Valuable assistance is derived from its agency in the detection of
adulterations. In the examination of flour, an article of so much importance
to all, the Microscope enables us to judge of the size and shape of the
starch-grains, their markings, their isolation and agglomeration, and thus to
distinguish the starch-grains of one meal from those of another. It detects
these and other ingredients, invisible to the naked eye, whether combined in
atoms or aggregated in crystals, which adulterate our food, our drink, and
our medicines. It discloses the lurking poison in the minute crystallisations
which its solutions precipitate. “It tells the murderer that the blood which
Page 13
stains him is that of his brother, and not of the other life which he pretends
to have taken; and as a witness against the criminal, it on one occasion
appealed to the very sand on which he trod at midnight.”
The zoologist finds in the Microscope a necessary coadjutor. To the
geologist it reveals, among a multiplicity of other facts, “that our large coal-
beds are the ruins of a gigantic vegetation; and the vast limestone rocks,
which are so abundant on the earth’s surface, are the catacombs of myriads
of animal tribes, too minute to be perceived by the unaided vision.”
By “conducting the eye to the confines of the visible form,” the Microscope
proves an effective auxiliary in defining the geometric properties of bodies.
Its influence as an instrument of research upon the structure of bodies has
been compared to that of the galvanic battery, in the hands of Davy, upon
Chemistry. It detects the smallest structural difference, heretofore
inappreciable, and, as an ally of Chemistry, enables us to discover the very
small changes of form and colour effected by test-fluids upon solids; and
dissects for us, so to speak, the most multiplex compounds. It opens out to
the mind an extended and vast tract, opulent in wonders, rich in beauties,
and boundless in extent.
The Microscope not only assists studies, and develops objects of profound
interest, but also opens up innumerable sources of entertainment and
amusement, in the ordinary conventional acceptation of these terms;
disclosing to us peculiarities and attractions in abundance; impressing us
with the wonderful and beautifully skilful adaptation of all parts of creation,
and filling our minds with additional reverence and admiration for the
beneficent and Almighty Creator.
The Author will conclude these prefatory observations with a few words in
explanation of his arrangements, by way of dealing with the instrument and
development of his subject. He has sought, in the volume that he now lays
before the public, to point out and elucidate at once in a practical manner
and in a popular style, the vast fund of utility and amusement which the
Microscope affords, and has endeavoured to touch upon most of the
interesting subjects for microscopic observation as fully as the restrictions
of a limited space, and the nature of the succinct summary, would permit.
To have dwelt upon each in complete detail would have necessitated the
to have taken; and as a witness against the criminal, it on one occasion
appealed to the very sand on which he trod at midnight.”
The zoologist finds in the Microscope a necessary coadjutor. To the
geologist it reveals, among a multiplicity of other facts, “that our large coal-
beds are the ruins of a gigantic vegetation; and the vast limestone rocks,
which are so abundant on the earth’s surface, are the catacombs of myriads
of animal tribes, too minute to be perceived by the unaided vision.”
By “conducting the eye to the confines of the visible form,” the Microscope
proves an effective auxiliary in defining the geometric properties of bodies.
Its influence as an instrument of research upon the structure of bodies has
been compared to that of the galvanic battery, in the hands of Davy, upon
Chemistry. It detects the smallest structural difference, heretofore
inappreciable, and, as an ally of Chemistry, enables us to discover the very
small changes of form and colour effected by test-fluids upon solids; and
dissects for us, so to speak, the most multiplex compounds. It opens out to
the mind an extended and vast tract, opulent in wonders, rich in beauties,
and boundless in extent.
The Microscope not only assists studies, and develops objects of profound
interest, but also opens up innumerable sources of entertainment and
amusement, in the ordinary conventional acceptation of these terms;
disclosing to us peculiarities and attractions in abundance; impressing us
with the wonderful and beautifully skilful adaptation of all parts of creation,
and filling our minds with additional reverence and admiration for the
beneficent and Almighty Creator.
The Author will conclude these prefatory observations with a few words in
explanation of his arrangements, by way of dealing with the instrument and
development of his subject. He has sought, in the volume that he now lays
before the public, to point out and elucidate at once in a practical manner
and in a popular style, the vast fund of utility and amusement which the
Microscope affords, and has endeavoured to touch upon most of the
interesting subjects for microscopic observation as fully as the restrictions
of a limited space, and the nature of the succinct summary, would permit.
To have dwelt upon each in complete detail would have necessitated the
Page 14
issue of many expensive volumes—and this would have entirely frustrated
the aim which the writer had in view; he has, therefore, contented himself
with the humble, but, he trusts, not useless, task of setting up a finger-post,
so to say, to direct the inquirer into the wider road. In the section of the
work devoted to the minuter portion of creation, he has ventured to dwell
somewhat longer, in the belief that that department is more especially the
province of the microscopist. He has arranged his topics under special
headings, and in separate chapters, for the sake of perspicuity and precision;
and has brought the ever-welcome aid of illustration to convey his
explanatory remarks more vividly to the minds of his readers.
Finally, it is the Author’s hope that, by the instrumentality of this volume,
he may possibly assist in bringing the Microscope, and its valuable and
delightful studies, before the general public in a more familiar,
compendious, and economical form than he found it at the period of its
publication, so that, in these days of a diffused taste for reading and the
spread of cheap publications, he may thus supply further exercise for the
intellectual faculties; contribute to the additional amusement and instruction
of the family circle, and aid the student of nature in investigating the
wonderful and exquisite works of the Almighty. If it shall be the good
fortune for this work, which is now confided with great diffidence to the
consideration of the public, to succeed, in however slight a degree, in
furthering this design, the Author will feel fully repaid for the amount of
time and labour expended.
London, May, 1854.
the aim which the writer had in view; he has, therefore, contented himself
with the humble, but, he trusts, not useless, task of setting up a finger-post,
so to say, to direct the inquirer into the wider road. In the section of the
work devoted to the minuter portion of creation, he has ventured to dwell
somewhat longer, in the belief that that department is more especially the
province of the microscopist. He has arranged his topics under special
headings, and in separate chapters, for the sake of perspicuity and precision;
and has brought the ever-welcome aid of illustration to convey his
explanatory remarks more vividly to the minds of his readers.
Finally, it is the Author’s hope that, by the instrumentality of this volume,
he may possibly assist in bringing the Microscope, and its valuable and
delightful studies, before the general public in a more familiar,
compendious, and economical form than he found it at the period of its
publication, so that, in these days of a diffused taste for reading and the
spread of cheap publications, he may thus supply further exercise for the
intellectual faculties; contribute to the additional amusement and instruction
of the family circle, and aid the student of nature in investigating the
wonderful and exquisite works of the Almighty. If it shall be the good
fortune for this work, which is now confided with great diffidence to the
consideration of the public, to succeed, in however slight a degree, in
furthering this design, the Author will feel fully repaid for the amount of
time and labour expended.
London, May, 1854.
Page 15
CONTENTS.
PART I.
PAGE
Early History of the Microscope 1
CHAPTER I.
Light—Its Propagation—Refraction—Spherical and Chromatic
Aberration—Human Eye—Formation of Images—Visual Angle
—Abbé’s Theory of Microscopic Vision—Definition of Aperture
—Numerical Aperture—Abbé’s Apertometer—Stereoscopic
Binocular Vision 12
CHAPTER II.
Simple and Compound Microscopes—Evolution of the Modern
Achromatic Microscope—Improvements in the Modern
Microscope: The Ross-Jackson, Powell and Lealand, Beck’s,
Baker’s, Pillischer, Zeiss, Leitz, Watson’s, Van Heurck’s
Edinburgh Students’, Swift’s, and Bacteriological 72
CHAPTER III.
Applied Optics—Eye-pieces—Achromatic Objectives and
Condensers—Magnifying Power of Eye-pieces and Objectives—
Method of Employing the Condenser—Its Illumination Mirror
—Accessories of the Microscope—Finders—Micrometers—
Camera-Lucida—Microscope in Position for Drawing—Abbé’s
Test-Plate—Micro-Photography—Polarisation of Light—The
Micro-Spectroscope 139
CHAPTER IV.
Practical Microscopy—Manipulation—Mode of Employing the 258
Microscope—Working Accessories—Methods of Preparing,
Hardening, Staining, and Section Cutting—Cutting Hard
PART I.
PAGE
Early History of the Microscope 1
CHAPTER I.
Light—Its Propagation—Refraction—Spherical and Chromatic
Aberration—Human Eye—Formation of Images—Visual Angle
—Abbé’s Theory of Microscopic Vision—Definition of Aperture
—Numerical Aperture—Abbé’s Apertometer—Stereoscopic
Binocular Vision 12
CHAPTER II.
Simple and Compound Microscopes—Evolution of the Modern
Achromatic Microscope—Improvements in the Modern
Microscope: The Ross-Jackson, Powell and Lealand, Beck’s,
Baker’s, Pillischer, Zeiss, Leitz, Watson’s, Van Heurck’s
Edinburgh Students’, Swift’s, and Bacteriological 72
CHAPTER III.
Applied Optics—Eye-pieces—Achromatic Objectives and
Condensers—Magnifying Power of Eye-pieces and Objectives—
Method of Employing the Condenser—Its Illumination Mirror
—Accessories of the Microscope—Finders—Micrometers—
Camera-Lucida—Microscope in Position for Drawing—Abbé’s
Test-Plate—Micro-Photography—Polarisation of Light—The
Micro-Spectroscope 139
CHAPTER IV.
Practical Microscopy—Manipulation—Mode of Employing the 258
Microscope—Working Accessories—Methods of Preparing,
Hardening, Staining, and Section Cutting—Cutting Hard
Page 16
Structures—Injecting Apparatus, Material, etc., employed in
Bacteriological Investigations—Warm Chambers and
Incubators—Preparing, Mounting, Cementing, and Collecting
Objects
PART II.
CHAPTER I.
Microscopic Forms of Life—Thallophytes, Pteridophyta,
Phanerogamæ—Structure and Properties of the Cell—
Pathogenic Fungi and Moulds—Parasitic Diseases of Plants,
Man, and Animals—Industrial Uses of Fungi and
Saccharomycetes—Desmidiaceæ and Diatomaceæ—Lichens,
Mosses, Ferns, Flowering Plants 353
CHAPTER II.
Sub-Kingdom Protozoa—Rhizopoda—Gromia and Foraminifera—
Infusoria—Ciliata—Rotifera—Porifera—Sponges 478
CHAPTER III.
Zoophytes—Cœlenterata—Medusæ—Corals—Hydrozoa—
Mollusca—Annulosa—Worms—Entozoa—Annelida—
Crustacea 515
CHAPTER IV.
Arthropoda—Insecta—Arachnida—Acarina—Ixodidæ—Mites
and Ticks 583
CHAPTER V.
Vertebrata—Internal and External Structures 633
CHAPTER VI.
The Mineral and Geological Kingdoms 670
APPENDIX.
Dr. Mercer on Illumination, and Abbé’s Theory—Micro-
Spectroscope—Formulæ, Methods, Cementing, Clearing,
Hardening, and Mounting—Tables, Metric and Thermometric 672
INDEX 691
Bacteriological Investigations—Warm Chambers and
Incubators—Preparing, Mounting, Cementing, and Collecting
Objects
PART II.
CHAPTER I.
Microscopic Forms of Life—Thallophytes, Pteridophyta,
Phanerogamæ—Structure and Properties of the Cell—
Pathogenic Fungi and Moulds—Parasitic Diseases of Plants,
Man, and Animals—Industrial Uses of Fungi and
Saccharomycetes—Desmidiaceæ and Diatomaceæ—Lichens,
Mosses, Ferns, Flowering Plants 353
CHAPTER II.
Sub-Kingdom Protozoa—Rhizopoda—Gromia and Foraminifera—
Infusoria—Ciliata—Rotifera—Porifera—Sponges 478
CHAPTER III.
Zoophytes—Cœlenterata—Medusæ—Corals—Hydrozoa—
Mollusca—Annulosa—Worms—Entozoa—Annelida—
Crustacea 515
CHAPTER IV.
Arthropoda—Insecta—Arachnida—Acarina—Ixodidæ—Mites
and Ticks 583
CHAPTER V.
Vertebrata—Internal and External Structures 633
CHAPTER VI.
The Mineral and Geological Kingdoms 670
APPENDIX.
Dr. Mercer on Illumination, and Abbé’s Theory—Micro-
Spectroscope—Formulæ, Methods, Cementing, Clearing,
Hardening, and Mounting—Tables, Metric and Thermometric 672
INDEX 691
Page 17
Page 18
DESCRIPTION OF PLATES,
COLOURED AND PLAIN.
FRONTISPIECE.
RADIOLARIA.
In this Plate Fig. 1 shows the elegant lattice-sphere of Rhizosphæra; Fig. 2
represents Sphærozoum, whose skeleton consists of loose spicules,
arranged tangentially; Actinomma, Fig. 3, possesses three concentric
lattice-spheres, joined by radiating spines; Figs. 4, 5, and 6, represent
Lithomespilus, Ommatocampe, and Carpocanium; Fig. 7 represents a
deep-sea form (Challengeria), whose oval case is formed of a regular,
very fine-meshed, network; Fig. 8 depicts the elegant lattice-sphere of
Heliosphæra; Figs. 9 and 10, Clathrocyclas and Dictyophimus.
PLATE I.—Page 400.
PROTOPHYTA. THALLOPHYTES.
Fig. 1. Peziza bicolor—2. Truffle: a. ascus of spores; b. mycelium—3.
Sphæria herbarum: a. piece of dead plant, with S. herbarum natural
size; b. section of same, slightly magnified; d. Ascus with spores, and
paraphyses more magnified—4. Peziza pygmæa—5. Apical form of
same—6. P. corpulasis: Ascus with spores and paraphyses, merely
given as a further illustration of structure in Peziza—7. Yeast healthy
—8. Yeast exhausted—9. Phyllactinia guttata—10. Yeast with favus
COLOURED AND PLAIN.
FRONTISPIECE.
RADIOLARIA.
In this Plate Fig. 1 shows the elegant lattice-sphere of Rhizosphæra; Fig. 2
represents Sphærozoum, whose skeleton consists of loose spicules,
arranged tangentially; Actinomma, Fig. 3, possesses three concentric
lattice-spheres, joined by radiating spines; Figs. 4, 5, and 6, represent
Lithomespilus, Ommatocampe, and Carpocanium; Fig. 7 represents a
deep-sea form (Challengeria), whose oval case is formed of a regular,
very fine-meshed, network; Fig. 8 depicts the elegant lattice-sphere of
Heliosphæra; Figs. 9 and 10, Clathrocyclas and Dictyophimus.
PLATE I.—Page 400.
PROTOPHYTA. THALLOPHYTES.
Fig. 1. Peziza bicolor—2. Truffle: a. ascus of spores; b. mycelium—3.
Sphæria herbarum: a. piece of dead plant, with S. herbarum natural
size; b. section of same, slightly magnified; d. Ascus with spores, and
paraphyses more magnified—4. Peziza pygmæa—5. Apical form of
same—6. P. corpulasis: Ascus with spores and paraphyses, merely
given as a further illustration of structure in Peziza—7. Yeast healthy
—8. Yeast exhausted—9. Phyllactinia guttata—10. Yeast with favus
Page 19
spores and mycelium of fungus—11. Favus ferment, with oïdium and
bacteria—12. Puccinia spores, growing in a saccharine solution—13.
Aerobic bacteria—14. Spores and mycelia from eczema produced by
yeast—15. Volvox globator—16. Amœboid condition of portion of
volvox—17. Puccinia buxi—18. Ditto, more enlarged—(17 to 20
illustrate Ascomycetes.)—19. Æcidium grossulariæ from transverse
section of leaf of currant: a. spermogones on upper surface; b.
perithecia with spores—20. Phragmidium bulbosum, development of
—21. Palmella parietina, trans. section through a spermogone,
showing green gonidia and spermatia escaping—22. Æcidium
berberida, from leaf of berberry—23. Vaucheria sessilis—24.
Stephanosphæra pluvialis: a. Full-grown example, germ cells spindle-
shaped with flagella; b. Resting-cell; c. division into four; d. Free-
swimming ciliated young specimen; e. Amœboid condition—25. a, b,
c, d, e, f and g, Development of lichen gonidia—26. Palmella stellaris
(lichen), vertical section through apothecium, showing asci, spores,
and paraphyses, with gonidia and filamentous medulla: a.
Spermatophore with spermatia—27. Moss gonidia assuming amœboid
form.
Typical forms of Protophyta; 7 to 14, modes of development or rudimentary
conditions; Confervoideæ, 23; Vaucheria, Stephanosphæra, 24; Volvox, 15,
&c.
PLATE II.—Page 412.
PROTOPHYTA. ALGÆ.
Fig. 27. Ceramium acanthonotum—28. Closterium, Triploceras gracilis—
29. Cosmarium radiatum—30. Micrasterias denticulata—31.
Docidium pristidæ—32. Callithamnion plumula—33. Diatoma, living:
a. Licmophora splendida; b. Achnanthes longipes; c. Grammatophora
marina. These figures are intended to show the general character of the
endochrome and growth of frustule—34. Callithamnion refractum—
35. Jungermannia albicans; b. representing elater and spores—36. Leaf
bacteria—12. Puccinia spores, growing in a saccharine solution—13.
Aerobic bacteria—14. Spores and mycelia from eczema produced by
yeast—15. Volvox globator—16. Amœboid condition of portion of
volvox—17. Puccinia buxi—18. Ditto, more enlarged—(17 to 20
illustrate Ascomycetes.)—19. Æcidium grossulariæ from transverse
section of leaf of currant: a. spermogones on upper surface; b.
perithecia with spores—20. Phragmidium bulbosum, development of
—21. Palmella parietina, trans. section through a spermogone,
showing green gonidia and spermatia escaping—22. Æcidium
berberida, from leaf of berberry—23. Vaucheria sessilis—24.
Stephanosphæra pluvialis: a. Full-grown example, germ cells spindle-
shaped with flagella; b. Resting-cell; c. division into four; d. Free-
swimming ciliated young specimen; e. Amœboid condition—25. a, b,
c, d, e, f and g, Development of lichen gonidia—26. Palmella stellaris
(lichen), vertical section through apothecium, showing asci, spores,
and paraphyses, with gonidia and filamentous medulla: a.
Spermatophore with spermatia—27. Moss gonidia assuming amœboid
form.
Typical forms of Protophyta; 7 to 14, modes of development or rudimentary
conditions; Confervoideæ, 23; Vaucheria, Stephanosphæra, 24; Volvox, 15,
&c.
PLATE II.—Page 412.
PROTOPHYTA. ALGÆ.
Fig. 27. Ceramium acanthonotum—28. Closterium, Triploceras gracilis—
29. Cosmarium radiatum—30. Micrasterias denticulata—31.
Docidium pristidæ—32. Callithamnion plumula—33. Diatoma, living:
a. Licmophora splendida; b. Achnanthes longipes; c. Grammatophora
marina. These figures are intended to show the general character of the
endochrome and growth of frustule—34. Callithamnion refractum—
35. Jungermannia albicans; b. representing elater and spores—36. Leaf
Page 20
with antheridia, or male elements, represented more magnified at a to
the left of the figure—37. Ceramium echinotum—38. Pleurosigma
angulatum, side view—39. Delesseria hypoglossum—40. Pleurosigma
angulatum, front view, endochrome not represented—41. Ceramium
flabelligerum.
PLATE III.—Page 479.
PROTOZOA.
Figs. 43, 44, 45, 46, 47, 48, 49, 50, 51, 52. These figures are from drawings
made by Major Owen, to illustrate forms of living Polycystina,
sketched from life; these convey a faint idea of the richly coloured
appearance of the natural structure; Figs. 48 to 52—53. Gregarina
lumbricorum, round form—54. Gregarina lumbricorum, the usual
elongated form—55. Gregarina serpulæ—56. Gregarina Sieboldii;
illustration of septate form, with reflexed hook-like processes—57.
Gregarina lumbricorum, encysted—58. Gregarina lumbricorum, more
advanced and pseudo-navicellæ forming—59. Gregarina lumbricorum,
free pseudo-navicella of—60, 61. Gregarina lumbricorum, amœboid
forms of—62. Cruciate sponge-spicule—63. Astromma Humboldtii—
64. Eözoon Canadense, represents appearance of a portion of the
natural size—65. Eözoon Canadense, magnified, showing portions of
cell-walls left uncoloured, the animal sarcode inhabiting it coloured
dark green as in nature, and converted by fossilisation into a silicious
mineral; the narrow bands passing between these are processes
(stolons) of the same substance—66. Actinophrys sol, budding—67.
Euglena viridis: a. contracted; b. elongated form—68. Acineta
tuberosa—69. Œcistes longicornis (Davis)—70. Oxytricha gibba (side
view)—71. Oxytricha pellionella—72. Thuricola valvata, expanded—
73. Cyclidium (glaucoma)—74. Oxytricha scintillans—75 to 79, 80 to
85, illustrate types of Foraminifera discovered by Major Owen, living
—75. Globigerina acerosa, n. sp., broken open to show interior—76.
Globigerina, n. sp., broken open to show interior—77. Globigerina
hirsuta—78. Globigerina universa—79 and 81. G. Bulloides—80.
the left of the figure—37. Ceramium echinotum—38. Pleurosigma
angulatum, side view—39. Delesseria hypoglossum—40. Pleurosigma
angulatum, front view, endochrome not represented—41. Ceramium
flabelligerum.
PLATE III.—Page 479.
PROTOZOA.
Figs. 43, 44, 45, 46, 47, 48, 49, 50, 51, 52. These figures are from drawings
made by Major Owen, to illustrate forms of living Polycystina,
sketched from life; these convey a faint idea of the richly coloured
appearance of the natural structure; Figs. 48 to 52—53. Gregarina
lumbricorum, round form—54. Gregarina lumbricorum, the usual
elongated form—55. Gregarina serpulæ—56. Gregarina Sieboldii;
illustration of septate form, with reflexed hook-like processes—57.
Gregarina lumbricorum, encysted—58. Gregarina lumbricorum, more
advanced and pseudo-navicellæ forming—59. Gregarina lumbricorum,
free pseudo-navicella of—60, 61. Gregarina lumbricorum, amœboid
forms of—62. Cruciate sponge-spicule—63. Astromma Humboldtii—
64. Eözoon Canadense, represents appearance of a portion of the
natural size—65. Eözoon Canadense, magnified, showing portions of
cell-walls left uncoloured, the animal sarcode inhabiting it coloured
dark green as in nature, and converted by fossilisation into a silicious
mineral; the narrow bands passing between these are processes
(stolons) of the same substance—66. Actinophrys sol, budding—67.
Euglena viridis: a. contracted; b. elongated form—68. Acineta
tuberosa—69. Œcistes longicornis (Davis)—70. Oxytricha gibba (side
view)—71. Oxytricha pellionella—72. Thuricola valvata, expanded—
73. Cyclidium (glaucoma)—74. Oxytricha scintillans—75 to 79, 80 to
85, illustrate types of Foraminifera discovered by Major Owen, living
—75. Globigerina acerosa, n. sp., broken open to show interior—76.
Globigerina, n. sp., broken open to show interior—77. Globigerina
hirsuta—78. Globigerina universa—79 and 81. G. Bulloides—80.
Page 21
Conochilus vorticella—82. Globigerina inflata, sinistral shell—83.
Pulvinulina Micheliniana—84. P. Canariensis—85. P. Menardii.
PLATE IV.—Page 514.
METAZOA. BRYOZOA.
Fig. 86. Hartea elegans—87. Side view of Synapta spicula—88.
Ophioglypha rosula (very immature specimen): a. Claw hooks; b.
palmate spicula. The development of this species is described by G.
Hodge, in “Transactions of Tyneside Naturalists’ Field-Club”—89.
Spine of a star-fish, particularly interesting as showing the reticular
calcareous network obtaining in this as in all other hard parts of the
Echinodermata—90. Very minute Spatangus, obtained from stomach
of a bream: many of the spines are gone, but the structure of the shell
is intact and forms a beautiful object, interesting in connection with the
source whence obtained—91. Ophioglypha neglecta: wriggling or
brittle starfish. The plate does not admit of a figure on a scale
sufficient to show the full beauty of this object—92. Tubularia
Dumortierii—93. Pedicellaria mandibulata from Uraster glacialis—94.
Pedicellaria forcepiforma, from the same—95. Cristatella mucedo; 96.
Edge-view of statoblast; 97. early stage in development of same—98.
Lophopus crystallinus—99. Plumatella repens with ova, on submerged
stem—100. Tænia echinococcus—101. Hydatids from human liver—
102. Bilharzia hæmatobia—103. Amphistoma conicum—104. Trichina
spiralis from fleshy part of Hambrc’ pork—105. Trichina spiralis male,
separated from muscle.—106, 107. Fasciola gigantea.
PLATE V.—Page 556.
MOLLUSCA.
Fig. 108. Velutina lævigata, portion of lingual membrane—109. Velutina
lævigata, part of mandible—110. Hybocystis blennius, portion of
Pulvinulina Micheliniana—84. P. Canariensis—85. P. Menardii.
PLATE IV.—Page 514.
METAZOA. BRYOZOA.
Fig. 86. Hartea elegans—87. Side view of Synapta spicula—88.
Ophioglypha rosula (very immature specimen): a. Claw hooks; b.
palmate spicula. The development of this species is described by G.
Hodge, in “Transactions of Tyneside Naturalists’ Field-Club”—89.
Spine of a star-fish, particularly interesting as showing the reticular
calcareous network obtaining in this as in all other hard parts of the
Echinodermata—90. Very minute Spatangus, obtained from stomach
of a bream: many of the spines are gone, but the structure of the shell
is intact and forms a beautiful object, interesting in connection with the
source whence obtained—91. Ophioglypha neglecta: wriggling or
brittle starfish. The plate does not admit of a figure on a scale
sufficient to show the full beauty of this object—92. Tubularia
Dumortierii—93. Pedicellaria mandibulata from Uraster glacialis—94.
Pedicellaria forcepiforma, from the same—95. Cristatella mucedo; 96.
Edge-view of statoblast; 97. early stage in development of same—98.
Lophopus crystallinus—99. Plumatella repens with ova, on submerged
stem—100. Tænia echinococcus—101. Hydatids from human liver—
102. Bilharzia hæmatobia—103. Amphistoma conicum—104. Trichina
spiralis from fleshy part of Hambrc’ pork—105. Trichina spiralis male,
separated from muscle.—106, 107. Fasciola gigantea.
PLATE V.—Page 556.
MOLLUSCA.
Fig. 108. Velutina lævigata, portion of lingual membrane—109. Velutina
lævigata, part of mandible—110. Hybocystis blennius, portion of
Page 22
palate—111. Sepia officinalis, portion of palate—112. Aplysia hybrida,
part of mandible—113. Loligo vulgaris, part of palate—114. Haliotis
tuberculatus, part of palate—115. Cistula catenata, part of palate—116.
Patella radiata, part of palate—117. Acmæa virginea, part of palate—
118. Cymba olla, part of palate—119. Scapander ligniarius—120.
Oneidoris bilamellata, part of palate—121. Testacella Maugei, part of
palate—122. Pleurobranchus plumula, part of mandible—123. Turbo
marmoratus, part of palate.
Lingual membranes of Mollusca; drawings made from specimens in the
collection formed by F. E. Edwards, Esq., now in the British Museum.
Typical examples of the numerous forms of Odontophors met with in
Gasteropod and Cephalopod Mollusca.
PLATE VI.—Page 582.
INSECTA.
Fig. 124. Egg of Caradrina morpheus, mottled rustic moth—125. Egg of
tortoise-shell butterfly, Vanessa urticæ—126. Egg of common
footman, Lithosia complanula—127. Egg of shark moth, Cucullia
umbratica—128. Maple-aphis—129. Egg shell of acarus, empty—130.
Egg of house-fly—131. Mouth of Tsetse-fly, Glossina morsitans—132.
Vapourer moth, Orgyia antiqua: antenna of male—133. Vapourer
moth: antenna of female; a. branch more magnified to show
rudimentary condition of the parts—134. Tortoise-shell butterfly; head
in profile, showing large compound eye, one of the palpi, and spiral
tongue—135. Tortoise-beetle, Cassida viridis; under surface of left
fore-foot, to show the bifurcate tenent appendages, one of which is
given at a more magnified. This form of appendage is characteristic of
the family. “West on Feet of Insects,” Linn. Trans. vol. xxiii. tab. 43-
136. Egg of blue argus butterfly, Polyommatus argus—137. Egg of
mottled umber, Erannis defoliaria—138. Egg of Ennomos erosaria,
thorn-moth—139. Egg of Aspilates gilvaria, straw-belle—140. Blow-
fly, Musca vomitoria: left fore-loot, under-surface, to show tenent
part of mandible—113. Loligo vulgaris, part of palate—114. Haliotis
tuberculatus, part of palate—115. Cistula catenata, part of palate—116.
Patella radiata, part of palate—117. Acmæa virginea, part of palate—
118. Cymba olla, part of palate—119. Scapander ligniarius—120.
Oneidoris bilamellata, part of palate—121. Testacella Maugei, part of
palate—122. Pleurobranchus plumula, part of mandible—123. Turbo
marmoratus, part of palate.
Lingual membranes of Mollusca; drawings made from specimens in the
collection formed by F. E. Edwards, Esq., now in the British Museum.
Typical examples of the numerous forms of Odontophors met with in
Gasteropod and Cephalopod Mollusca.
PLATE VI.—Page 582.
INSECTA.
Fig. 124. Egg of Caradrina morpheus, mottled rustic moth—125. Egg of
tortoise-shell butterfly, Vanessa urticæ—126. Egg of common
footman, Lithosia complanula—127. Egg of shark moth, Cucullia
umbratica—128. Maple-aphis—129. Egg shell of acarus, empty—130.
Egg of house-fly—131. Mouth of Tsetse-fly, Glossina morsitans—132.
Vapourer moth, Orgyia antiqua: antenna of male—133. Vapourer
moth: antenna of female; a. branch more magnified to show
rudimentary condition of the parts—134. Tortoise-shell butterfly; head
in profile, showing large compound eye, one of the palpi, and spiral
tongue—135. Tortoise-beetle, Cassida viridis; under surface of left
fore-foot, to show the bifurcate tenent appendages, one of which is
given at a more magnified. This form of appendage is characteristic of
the family. “West on Feet of Insects,” Linn. Trans. vol. xxiii. tab. 43-
136. Egg of blue argus butterfly, Polyommatus argus—137. Egg of
mottled umber, Erannis defoliaria—138. Egg of Ennomos erosaria,
thorn-moth—139. Egg of Aspilates gilvaria, straw-belle—140. Blow-
fly, Musca vomitoria: left fore-loot, under-surface, to show tenent
Page 23
hairs; a b more magnified; a from below, b from the side—141.
House-fly larva—142. Amara communis: left fore-foot, under-surface,
to show form of tenent appendages, of which one is given more
magnified at a. These, in ground beetles, are met with only in the
males, believed to be used for sexual purposes. These appendages are
carefully protected when not in use, as explained by West—143.
Ephydra riparia: left fore-foot, under-surface. This fly is met with
sometimes in immense numbers on the water in salt-marshes; it has no
power of climbing on glass, as seen by the structure of the tenent hairs;
the central tactile organ also is peculiar, the whole acting as a float, one
attached to each foot, enabling the fly to rest on the surface of the
water; a. an enlarged external hair—144. Egg of bot-fly, the larva just
escaping—145. Egg of parasite of pheasant—146. Egg of Scatophaga
—147. Egg of parasite of magpie—148. Egg of Jodis vernaria, small
emerald moth.
PLATE VII.—Page 633.
VERTEBRATA.
Fig. 149. Toe of mouse, integuments, bone of foot, and vessels—150.
Tongue of mouse, showing erectile papillæ and muscular layer—151.
Brain of rat, showing vascular supply—152. Vertical section of tongue
of cat, fungi-form papillæ and capillary loops passing into them,
vessels—153. Kidney of cat, showing Malpighian turfts and arteries—
154. Small intestine of rat, with villi and layer of mucous membrane
exposed—155. Nose of mouse, showing vascular supply to roots of
whiskers—156. Vascular supply to internal gill of tadpole, during one
phase of development—157. Section through sclerotic coat and retina
of cat’s eye, showing vascular supply of choroid vessels cut cross-
ways—158. Interior of fully-developed tadpole, exhibiting heart,
vascular arrangement and vascular system throughout body and tail.
This plate is designed to show the value, in certain cases, of injected
preparations in the delineation of animal structures. By thus artificially
House-fly larva—142. Amara communis: left fore-foot, under-surface,
to show form of tenent appendages, of which one is given more
magnified at a. These, in ground beetles, are met with only in the
males, believed to be used for sexual purposes. These appendages are
carefully protected when not in use, as explained by West—143.
Ephydra riparia: left fore-foot, under-surface. This fly is met with
sometimes in immense numbers on the water in salt-marshes; it has no
power of climbing on glass, as seen by the structure of the tenent hairs;
the central tactile organ also is peculiar, the whole acting as a float, one
attached to each foot, enabling the fly to rest on the surface of the
water; a. an enlarged external hair—144. Egg of bot-fly, the larva just
escaping—145. Egg of parasite of pheasant—146. Egg of Scatophaga
—147. Egg of parasite of magpie—148. Egg of Jodis vernaria, small
emerald moth.
PLATE VII.—Page 633.
VERTEBRATA.
Fig. 149. Toe of mouse, integuments, bone of foot, and vessels—150.
Tongue of mouse, showing erectile papillæ and muscular layer—151.
Brain of rat, showing vascular supply—152. Vertical section of tongue
of cat, fungi-form papillæ and capillary loops passing into them,
vessels—153. Kidney of cat, showing Malpighian turfts and arteries—
154. Small intestine of rat, with villi and layer of mucous membrane
exposed—155. Nose of mouse, showing vascular supply to roots of
whiskers—156. Vascular supply to internal gill of tadpole, during one
phase of development—157. Section through sclerotic coat and retina
of cat’s eye, showing vascular supply of choroid vessels cut cross-
ways—158. Interior of fully-developed tadpole, exhibiting heart,
vascular arrangement and vascular system throughout body and tail.
This plate is designed to show the value, in certain cases, of injected
preparations in the delineation of animal structures. By thus artificially
Page 24
restoring the blood and distending the tissues, a better idea is obtained of
the relative condition of parts during life.
PLATE VIII.—Page 220.
POLARISCOPE OBJECTS.
Fig. 158. New Red Sandstone—159. Quartz—163. Granite—161. Sulph.
Copper—162. Saliginine—163. Sulph. Iron and Cobalt, crystallized in
the way described by Thomas—164. Borax—165. Sulph. Nickel and
Potash—166. Kreatine—167. Starch granules—168. Aspartic Acid—
169. Fibro-cells, orchid.—170. Equisetum cuticle—171. Holothuria
spicula, Australia—172. Holothuria spicula, Port Essington—173.
Deutzia scabra; upper and under surface—174. Cat’s tongue, process
—175. Prawn shell, exuvia with crystals of lime—176. Grayling scale
—177. Scyllium caniculum scale—178. Rhinoceros horn, transverse
section—179. Horse hoof—180. Dytiscus, elytra with crystals of lime.
PLATE IX.—Page 362.
TYPICAL PLATE OF BACTERIA AND SCHIZOMYCETES.
Fig. 1. Cocci, singly, and varying in size—2. Cocci in chains or rosaries
(streptococcus)—3. Cocci in a mass (staphylococcus)—4 and 5. Cocci
in pairs (diplococcus)—6. Cocci in groups of four (merismopedia)—7.
Cocci in packets (sarcina)—8. Bacterium termo—9. Bacterium termo
× 4000 (Dallinger and Drysdale)—10. Bacterium septicæmiæ
hæmorrhagicæ—11. Bacterium pneumoniæ crouposæ—12. Bacillus
subtilis—13. Bacillus murisepticus—14. Bacillus diphtheriæ—15.
Bacillus typhosus (Eberth)—16. Spirillum undula (Cohn)—17.
Spirillum volutans (Cohn)—18. Spirillum choleræ Asiaticæ—19.
Spirillum Obermeieri (Koch)—20. Spirochæta plicatilis (Flügge)—21.
Vibrio rugula (Prazmowski)—22. Cladothrix Försteri (Cohn)—23.
Cladothrix dichotoma (Cohn)—24. Monas Okenii (Cohn)—25. Monas
the relative condition of parts during life.
PLATE VIII.—Page 220.
POLARISCOPE OBJECTS.
Fig. 158. New Red Sandstone—159. Quartz—163. Granite—161. Sulph.
Copper—162. Saliginine—163. Sulph. Iron and Cobalt, crystallized in
the way described by Thomas—164. Borax—165. Sulph. Nickel and
Potash—166. Kreatine—167. Starch granules—168. Aspartic Acid—
169. Fibro-cells, orchid.—170. Equisetum cuticle—171. Holothuria
spicula, Australia—172. Holothuria spicula, Port Essington—173.
Deutzia scabra; upper and under surface—174. Cat’s tongue, process
—175. Prawn shell, exuvia with crystals of lime—176. Grayling scale
—177. Scyllium caniculum scale—178. Rhinoceros horn, transverse
section—179. Horse hoof—180. Dytiscus, elytra with crystals of lime.
PLATE IX.—Page 362.
TYPICAL PLATE OF BACTERIA AND SCHIZOMYCETES.
Fig. 1. Cocci, singly, and varying in size—2. Cocci in chains or rosaries
(streptococcus)—3. Cocci in a mass (staphylococcus)—4 and 5. Cocci
in pairs (diplococcus)—6. Cocci in groups of four (merismopedia)—7.
Cocci in packets (sarcina)—8. Bacterium termo—9. Bacterium termo
× 4000 (Dallinger and Drysdale)—10. Bacterium septicæmiæ
hæmorrhagicæ—11. Bacterium pneumoniæ crouposæ—12. Bacillus
subtilis—13. Bacillus murisepticus—14. Bacillus diphtheriæ—15.
Bacillus typhosus (Eberth)—16. Spirillum undula (Cohn)—17.
Spirillum volutans (Cohn)—18. Spirillum choleræ Asiaticæ—19.
Spirillum Obermeieri (Koch)—20. Spirochæta plicatilis (Flügge)—21.
Vibrio rugula (Prazmowski)—22. Cladothrix Försteri (Cohn)—23.
Cladothrix dichotoma (Cohn)—24. Monas Okenii (Cohn)—25. Monas
Page 25
Warmingii (Cohn)—26. Rhabdomonas rosea (Cohn)—27. Spore-
formation of Bacillus alvei—28. Spore-formation (Bacillus anthracis)
—29. Spore-formation in bacilli cultivated from rotten melon (Fränkel
and Pfeiffer)—30. Spore-formation in bacilli cultivated from earth
(Fränkel and Pfeiffer)—31. Involution-form of Crenothrix (Zopf)—32.
Involution-forms of Vibrio serpens (Warming)—33. Involution-forms
of Vibrio rugula (Warming)—34. Involution-forms of Clostridium
polymyxa (Prazmowski)—35. Involution-forms of Spirillum choleræ
Asiaticæ—36. Involution-forms of Bacterium aceti (Zopf and Hansen)
—37. Spirulina-form of Beggiatoa alba (Zopf)—38. Various thread-
forms of Bacterium merismopedioides (Zopf)—39. False-branching of
Cladothrix (Zopf).
PLATE X.—Page 420.
DESMIDIACEÆ.
Fig. 1. Euastrum oblongum—2. Micrasterias rotata—3. Desmidium
quadrangulatum—4. Didymoprium Grevillii—5. Micrasterias,
sporangium of—6. Didymoprium Borreri—7. Cosmarium Ralfsii—8,
9. Xanthidiæ—10. X. armatum—11. Cosmarium crenatum—12. C.
Sphærozosma vertebratum—13, 17. Sporangia of Cosmarium—14. X.
fasiculatum—18. Staurastrum hirsutum—19. Arthrodesmus
convergens—15. Staurastrum tumidum—16. Staurastrum dilitatum—
21. Penium—22. Euastrum Didelta—23. Docidium clavatum—24.
Pediastrum biradiatum—25. Closterium, showing conjugation or self-
division—26. Volvox, parent cell about to break up—27. Penium
Jennerii—28. Aptogonum desmidium—29. Pediastrum pertusum—30.
Ankistrodesmus falcatus—31. Parent cell of Closterium—32.
Staurastrum gracilis.—33. Conjugation of Penium margaritaceum—
34. Spirotænia—35. Closterium
PLATE XI.—Page 428.
formation of Bacillus alvei—28. Spore-formation (Bacillus anthracis)
—29. Spore-formation in bacilli cultivated from rotten melon (Fränkel
and Pfeiffer)—30. Spore-formation in bacilli cultivated from earth
(Fränkel and Pfeiffer)—31. Involution-form of Crenothrix (Zopf)—32.
Involution-forms of Vibrio serpens (Warming)—33. Involution-forms
of Vibrio rugula (Warming)—34. Involution-forms of Clostridium
polymyxa (Prazmowski)—35. Involution-forms of Spirillum choleræ
Asiaticæ—36. Involution-forms of Bacterium aceti (Zopf and Hansen)
—37. Spirulina-form of Beggiatoa alba (Zopf)—38. Various thread-
forms of Bacterium merismopedioides (Zopf)—39. False-branching of
Cladothrix (Zopf).
PLATE X.—Page 420.
DESMIDIACEÆ.
Fig. 1. Euastrum oblongum—2. Micrasterias rotata—3. Desmidium
quadrangulatum—4. Didymoprium Grevillii—5. Micrasterias,
sporangium of—6. Didymoprium Borreri—7. Cosmarium Ralfsii—8,
9. Xanthidiæ—10. X. armatum—11. Cosmarium crenatum—12. C.
Sphærozosma vertebratum—13, 17. Sporangia of Cosmarium—14. X.
fasiculatum—18. Staurastrum hirsutum—19. Arthrodesmus
convergens—15. Staurastrum tumidum—16. Staurastrum dilitatum—
21. Penium—22. Euastrum Didelta—23. Docidium clavatum—24.
Pediastrum biradiatum—25. Closterium, showing conjugation or self-
division—26. Volvox, parent cell about to break up—27. Penium
Jennerii—28. Aptogonum desmidium—29. Pediastrum pertusum—30.
Ankistrodesmus falcatus—31. Parent cell of Closterium—32.
Staurastrum gracilis.—33. Conjugation of Penium margaritaceum—
34. Spirotænia—35. Closterium
PLATE XI.—Page 428.
Page 26
DIATOMACEÆ.
Fig. 1. Arachnoidiscus—2. Actinocyclus (Bermuda)—3. Cocconeis (Algoa
Bay)—4. Coccinodiscus (Bermuda)—5. Isthmia enervis—6.
Zygoceros rhombus—7. Campilodiscus clypeus—8. Biddulphia—9.
Gallionella sulcata—10. Triceratium, found in Thames mud—11.
Gomphonema geminatum, with their stalk-like attachments—12.
Dictyocha fibula—13. Eunotia—14. Cocconema—15. Fragilaria
pectinalis—16. Meridion circulare—17. Diatoma flocculosum.
PLATE XII.—Page 438.
MICRO-PHOTOGRAPH OF TEST DIATOMS.
Taken with Zeiss’s 3 mm. N.A. 1·40 by Mr. A. A. Carvell for the Author.
Fig. 1. Portion of Surirella gemma, magnified × 1,000—2. Broken Frustule
of Pleurosigma angulatum, × 750—3 and 5. Triceratium favus ×—
1,000—4. Navicula rhomboides × 1,300—6. Pleurosigma formosum,
showing black dots—7. P. formosum, showing white dots, × 750.
PLATE XIII.—Page 454.
PHANEROGAMIÆ—ELEMENTARY TISSUE OF PLANTS.
Fig. 1. Elementary ovid cells—2. Branching tissue—2A and 3. Spiral
vessels from Opuntia vulgaris—4. Stellate tissue, section of rush—5.
Mushroom spawn—6. Starch from Tous-les-mois—7. Starch from
sago—8. Starch from rice—9. Wheat-starch—10. Rhubarb starch in
isolated cells—11. Maize-starch—12. Oat-starch—13. Barley-starch—
14. Section of Potato cells, filled with healthy starch—15. Potato
starch more highly magnified—16. Section of Potato with nearly all
starch absent—17. Potato with starch destroyed by fungoid disease—
Fig. 1. Arachnoidiscus—2. Actinocyclus (Bermuda)—3. Cocconeis (Algoa
Bay)—4. Coccinodiscus (Bermuda)—5. Isthmia enervis—6.
Zygoceros rhombus—7. Campilodiscus clypeus—8. Biddulphia—9.
Gallionella sulcata—10. Triceratium, found in Thames mud—11.
Gomphonema geminatum, with their stalk-like attachments—12.
Dictyocha fibula—13. Eunotia—14. Cocconema—15. Fragilaria
pectinalis—16. Meridion circulare—17. Diatoma flocculosum.
PLATE XII.—Page 438.
MICRO-PHOTOGRAPH OF TEST DIATOMS.
Taken with Zeiss’s 3 mm. N.A. 1·40 by Mr. A. A. Carvell for the Author.
Fig. 1. Portion of Surirella gemma, magnified × 1,000—2. Broken Frustule
of Pleurosigma angulatum, × 750—3 and 5. Triceratium favus ×—
1,000—4. Navicula rhomboides × 1,300—6. Pleurosigma formosum,
showing black dots—7. P. formosum, showing white dots, × 750.
PLATE XIII.—Page 454.
PHANEROGAMIÆ—ELEMENTARY TISSUE OF PLANTS.
Fig. 1. Elementary ovid cells—2. Branching tissue—2A and 3. Spiral
vessels from Opuntia vulgaris—4. Stellate tissue, section of rush—5.
Mushroom spawn—6. Starch from Tous-les-mois—7. Starch from
sago—8. Starch from rice—9. Wheat-starch—10. Rhubarb starch in
isolated cells—11. Maize-starch—12. Oat-starch—13. Barley-starch—
14. Section of Potato cells, filled with healthy starch—15. Potato
starch more highly magnified—16. Section of Potato with nearly all
starch absent—17. Potato with starch destroyed by fungoid disease—
Page 27
18. Ciliated spermagones—19. Hairs of stinging-nettle—20. Section of
cellular parenchyma of ripe strawberry.
PLATE XIV.—Page 472.
STELLATE AND CRYSTALLINE TISSUE.
Fig. 1. Epidermis of husk of wheat, spiral vessels and silicious crystals—2.
Section of cane, silicious cell walls, internal portion filled with
granular bodies—3. Cuticular layer of the onion, showing crystals of
calcium carbonate and oxalate—4. Cells of garden rhubarb, with
crystalline bodies and raphides—4a. Another layer filled with starch
grains—5. Section of pear, testa, sclerogenous and granular tissue—6.
Stellate hairs, sinuous cells and silicious parenchyma of leaf of Deutzia
scabra, under surface—7. Silicious cuticle layer of grass, Pharus
cristatus.
PLATE XV.—Page 482.
RHIZOPODA.—GROMIA.—FORAMINIFERA.
Fig. 1. Astrorhiza limicola—2. Lieberkühnia paludosa—3. Micro-gromia
socialis undergoing fission—4. A colony of Hertwig’s Micro-gromia
socialis—5. G. Lieberkühnia—6. Egg-shaped Gromia, G. oviformis,
with pseudopodia extended, magnified 500 diameters. “Hertwig Ueber
Micro-gromia, archiv. für Mickr. Anat. bdx.”
PLATE XVI.—Page 510.
SPONGE SPICULES.
cellular parenchyma of ripe strawberry.
PLATE XIV.—Page 472.
STELLATE AND CRYSTALLINE TISSUE.
Fig. 1. Epidermis of husk of wheat, spiral vessels and silicious crystals—2.
Section of cane, silicious cell walls, internal portion filled with
granular bodies—3. Cuticular layer of the onion, showing crystals of
calcium carbonate and oxalate—4. Cells of garden rhubarb, with
crystalline bodies and raphides—4a. Another layer filled with starch
grains—5. Section of pear, testa, sclerogenous and granular tissue—6.
Stellate hairs, sinuous cells and silicious parenchyma of leaf of Deutzia
scabra, under surface—7. Silicious cuticle layer of grass, Pharus
cristatus.
PLATE XV.—Page 482.
RHIZOPODA.—GROMIA.—FORAMINIFERA.
Fig. 1. Astrorhiza limicola—2. Lieberkühnia paludosa—3. Micro-gromia
socialis undergoing fission—4. A colony of Hertwig’s Micro-gromia
socialis—5. G. Lieberkühnia—6. Egg-shaped Gromia, G. oviformis,
with pseudopodia extended, magnified 500 diameters. “Hertwig Ueber
Micro-gromia, archiv. für Mickr. Anat. bdx.”
PLATE XVI.—Page 510.
SPONGE SPICULES.
Page 28
Fig. 1. A portion of sponge, Halichondria simulans, showing silicious
spicula imbedded in the sarcode matrix—2. Spicula divested of its
matrix by acid—3. Gemmule Spongilla fluviatallis enclosed in spicula
—4. Birotulate spicula from same—5. Gemmule after being steeped in
acid showing reticulated coating of birotulate spicula—6. Gemmules
of Geodia—7. Gemmule in more advanced stage of growth—8.
Skeleton of the acerate form covered by rows of spines—9. Showing
rings of growth and horny covering, and bundles of spicula of the
genus Verongia—10. Sphero-stellate spicula of Tethya—11.
Tricuspidanchorate and sphero-stellate spicula—12. Acuate-bi-clavate
and other forms of spicula from Geodia—13. Clavate spicula covered
with short spines.
PLATE XVII.—Page 518.
ZOOPHYTES, ASTEROIDS, NUDIBRANCHS, AND ECHINOIDS.
Fig. 1. a. Astrophyton scutatum—b. Doris pinnatifida, back and side view
—c. Æquorea Forbesina—d. Medusæ bud—e. Thaumantias corynetes
—f. Echinus in an early free stage—g. Echinus sphæra—h. Cydippe
pyleus—i. Ascidiæ—k. Botryllus violaceus, on a Fucus—l. Corystes
cassivelaunus—m. Eurynome aspera—n. Ophiocoma rosula—o.
Pagurus Prideauxii—p. Ebalia Permantii.
PLATE XVIII.—Page 558.
SHELLS OF MOLLUSCA.
Fig. 1. Transverse section of spine of Echinus—2. Another section of
Echinus, showing reticulated structure, the calcareous portion
dissolved out by acid—3. Horizontal section of shell of Haliotis
splendens, showing stellate pigment—4. Shell of crab with granules in
articular layer—5. Another section of same shell, showing hexagonal
structure—6. Horizontal section of coach-spring shell, Terebratulata
spicula imbedded in the sarcode matrix—2. Spicula divested of its
matrix by acid—3. Gemmule Spongilla fluviatallis enclosed in spicula
—4. Birotulate spicula from same—5. Gemmule after being steeped in
acid showing reticulated coating of birotulate spicula—6. Gemmules
of Geodia—7. Gemmule in more advanced stage of growth—8.
Skeleton of the acerate form covered by rows of spines—9. Showing
rings of growth and horny covering, and bundles of spicula of the
genus Verongia—10. Sphero-stellate spicula of Tethya—11.
Tricuspidanchorate and sphero-stellate spicula—12. Acuate-bi-clavate
and other forms of spicula from Geodia—13. Clavate spicula covered
with short spines.
PLATE XVII.—Page 518.
ZOOPHYTES, ASTEROIDS, NUDIBRANCHS, AND ECHINOIDS.
Fig. 1. a. Astrophyton scutatum—b. Doris pinnatifida, back and side view
—c. Æquorea Forbesina—d. Medusæ bud—e. Thaumantias corynetes
—f. Echinus in an early free stage—g. Echinus sphæra—h. Cydippe
pyleus—i. Ascidiæ—k. Botryllus violaceus, on a Fucus—l. Corystes
cassivelaunus—m. Eurynome aspera—n. Ophiocoma rosula—o.
Pagurus Prideauxii—p. Ebalia Permantii.
PLATE XVIII.—Page 558.
SHELLS OF MOLLUSCA.
Fig. 1. Transverse section of spine of Echinus—2. Another section of
Echinus, showing reticulated structure, the calcareous portion
dissolved out by acid—3. Horizontal section of shell of Haliotis
splendens, showing stellate pigment—4. Shell of crab with granules in
articular layer—5. Another section of same shell, showing hexagonal
structure—6. Horizontal section of coach-spring shell, Terebratulata
Page 29
rubicunda, showing radiating perforations—7. Transverse section of
shell of the Pinna ingens—8. Crystals of carbonate of lime, from
oyster shell.
PLATE XIX.—Page 636.
VERTEBRATA.
Fig. 1. a. Spheroidal epithelium cells, filled with central nuclei and granular
matter; b. mucous membrane of stomach, showing cells, with open
mouths of tubes at the bottom of each, magnified 50 diameters—2. a.
Diagram of a portion of the involuted mucous membrane, showing
continuation of its elements in the follicles and villi, with a nerve
entering the submucous tissue. The upper surface of one villus is
covered with cylindrical epithelium; the other denuded, and with dark
line of basement membrane running around it; b. epithelium cells,
separated and magnified 200 diameters, a central nucleus, with a
nucleolus, seen in centre; c. pavement epithelium cells, from the
mucous membrane of bronchial or air tubes with nuclei, and nucleoli
in some; d. vibratile or ciliated epithelium, nuclei visible, and cilia at
the upper free surface, magnified 200 diameters—3. a. is one of the
tubular follicles from a pig’s stomach, cut obliquely to display upper
part of cavity, and the cylindrical epithelium forming its walls, a few
cells detached; b. shows a section of a lymphatic, with capillary blood-
vessels, distributed beneath the mucous surfaces—4. Cells of adipose
tissue, or fat, magnified 100 diameters—5. a single fat-cell separated,
and magnified 250 diameters—6. A capillary of blood-vessels
distributed through tissue—7. Section of the Tendo-Achillis as it joins
the cartilage, showing stellate cells of tendon, seen to be gradually
coalescing to form round or oval cells of cartilage—8. A vertical
section of cartilage, with clusters of cells arranged in columns previous
to their conversion into bone—9. A small transverse section of the
same, showing the gradual change of the cartilage cells at a. into the
true bone cells, lacunæ, at b. with characteristic canaliculi—10. A
stellate nerve corpuscle, with tubular processes issuing forth, at a.
shell of the Pinna ingens—8. Crystals of carbonate of lime, from
oyster shell.
PLATE XIX.—Page 636.
VERTEBRATA.
Fig. 1. a. Spheroidal epithelium cells, filled with central nuclei and granular
matter; b. mucous membrane of stomach, showing cells, with open
mouths of tubes at the bottom of each, magnified 50 diameters—2. a.
Diagram of a portion of the involuted mucous membrane, showing
continuation of its elements in the follicles and villi, with a nerve
entering the submucous tissue. The upper surface of one villus is
covered with cylindrical epithelium; the other denuded, and with dark
line of basement membrane running around it; b. epithelium cells,
separated and magnified 200 diameters, a central nucleus, with a
nucleolus, seen in centre; c. pavement epithelium cells, from the
mucous membrane of bronchial or air tubes with nuclei, and nucleoli
in some; d. vibratile or ciliated epithelium, nuclei visible, and cilia at
the upper free surface, magnified 200 diameters—3. a. is one of the
tubular follicles from a pig’s stomach, cut obliquely to display upper
part of cavity, and the cylindrical epithelium forming its walls, a few
cells detached; b. shows a section of a lymphatic, with capillary blood-
vessels, distributed beneath the mucous surfaces—4. Cells of adipose
tissue, or fat, magnified 100 diameters—5. a single fat-cell separated,
and magnified 250 diameters—6. A capillary of blood-vessels
distributed through tissue—7. Section of the Tendo-Achillis as it joins
the cartilage, showing stellate cells of tendon, seen to be gradually
coalescing to form round or oval cells of cartilage—8. A vertical
section of cartilage, with clusters of cells arranged in columns previous
to their conversion into bone—9. A small transverse section of the
same, showing the gradual change of the cartilage cells at a. into the
true bone cells, lacunæ, at b. with characteristic canaliculi—10. A
stellate nerve corpuscle, with tubular processes issuing forth, at a.
Page 30
filled with corpuscles containing black pigment, above which is a
corpuscle the nucleus of which is seen to have nucleoli; at b. a
corpuscle enclosed within sheath, and filled with granular matter taken
from the root of a spinal nerve—11. The continuity of muscle, the
upper portion, with connective tissue of the lower portion, from the
tongue of a lamb—12. Branched muscle, ending in stellate connective
cells, from the upper lip of the rat—13. Choroidal black pigment-cells
from the human eye.
PLATE XX.—Page 658.
BONE STRUCTURE.
Figs. 1. and 2. Transverse section of the human clavicle (collar bone),
showing Haversian canals, concentric laminæ, and concentric
arrangement of bone cells—3. Transverse section of the femur of an
ostrich—4. Transverse section of humerus (fore-arm) bone of a turtle,
Chelonia mydas—5. Horizontal section of the lower jaw-bone of a
conger eel, in which no Haversian canals are present—6. A portion of
the cranium of a siren, Siren lacertina—7. Portion of bone taken from
the shaft of humerus of a Pterodactyle, showing elongated bone-cells
characteristic of the order Reptilia—8. Horizontal section of a scale, or
flattened spine, from the skin of a Trygon (sting-ray), showing large
Haversian canals, numerous wavy parallel tubes, also bone-cells with
canaliculi communicating as in dentine.
corpuscle the nucleus of which is seen to have nucleoli; at b. a
corpuscle enclosed within sheath, and filled with granular matter taken
from the root of a spinal nerve—11. The continuity of muscle, the
upper portion, with connective tissue of the lower portion, from the
tongue of a lamb—12. Branched muscle, ending in stellate connective
cells, from the upper lip of the rat—13. Choroidal black pigment-cells
from the human eye.
PLATE XX.—Page 658.
BONE STRUCTURE.
Figs. 1. and 2. Transverse section of the human clavicle (collar bone),
showing Haversian canals, concentric laminæ, and concentric
arrangement of bone cells—3. Transverse section of the femur of an
ostrich—4. Transverse section of humerus (fore-arm) bone of a turtle,
Chelonia mydas—5. Horizontal section of the lower jaw-bone of a
conger eel, in which no Haversian canals are present—6. A portion of
the cranium of a siren, Siren lacertina—7. Portion of bone taken from
the shaft of humerus of a Pterodactyle, showing elongated bone-cells
characteristic of the order Reptilia—8. Horizontal section of a scale, or
flattened spine, from the skin of a Trygon (sting-ray), showing large
Haversian canals, numerous wavy parallel tubes, also bone-cells with
canaliculi communicating as in dentine.
Page 31
ERRATA.
Prefaces, page vi., line 22 Insert “a” into “admitted.”
Prefaces, page x., line 13 Insert “the” before “assistance.”
Prefaces, page xii. Insert “for” at commencement of line 24.
Page 33, line 13 For “Rabbit” read “Kitten.”
Page 486, 4th line from bottom Strike out “The late.”
Page 511, two lines from
bottom For “Plate XIII.” read “Plate XVI.”
Page 584, 5th line from bottom Insert “Stalk-Eyed” before
“crustaceans.”
Page 624, line 12 For “or” read “and.”
Page 633, Plate VII. Numbering of figures—
For “152” read “158.”
For “152a” read “152.”
(Professor Abbe, erroneously referred to more than once as “the late” is, the
author is happy to say, in excellent health).
Prefaces, page vi., line 22 Insert “a” into “admitted.”
Prefaces, page x., line 13 Insert “the” before “assistance.”
Prefaces, page xii. Insert “for” at commencement of line 24.
Page 33, line 13 For “Rabbit” read “Kitten.”
Page 486, 4th line from bottom Strike out “The late.”
Page 511, two lines from
bottom For “Plate XIII.” read “Plate XVI.”
Page 584, 5th line from bottom Insert “Stalk-Eyed” before
“crustaceans.”
Page 624, line 12 For “or” read “and.”
Page 633, Plate VII. Numbering of figures—
For “152” read “158.”
For “152a” read “152.”
(Professor Abbe, erroneously referred to more than once as “the late” is, the
author is happy to say, in excellent health).
Page 32
THE MICROSCOPE.
Page 33
PART I.
Early History of the Microscope.
The instrument known as the Microscope derives its designation from two
Greek words, μικρὸς (mikros), small, and σκοπέω (skopeo), to see or
observe; and is an optical instrument by means of which objects are so
magnified that details invisible or indistinct to the naked eye are clearly
seen. Its origin, so far as yet can be traced back, seems to be of a doubtful
nature. It is tolerably certain the ancients had little or no conception of the
magnifying power of lenses; this may be surmised from their writings. The
elder Pliny incidentally states that the physicians of his day cauterised by
means of “a globe of crystal.” The learned Greek physician, Galen,
however, demonstrates conclusively that in the first and second centuries of
our era the use of magnifying lenses was quite unknown either to Greek or
Roman. Moreover, the writings of Archimedes, Ptolemy, and other learned
men, show that, although they had some idea of the action of refraction at
plane surfaces, as of water, yet of the refraction at curved surfaces they had
formed no conception. Indeed, they refer quite indiscriminately to the
spherical form, or the disc, or the plane surface of the water, but not one of
them speaks of the lenticular form, or the curvature of their surfaces.
As to the more powerful optical instruments, the telescope and microscope,
although it would appear that Alhazen in the 10th or 11th century, Roger
Bacon in the 13th, and Fracastoro and Baptist Porta in the 16th, had formed
some idea that lenses might be made and combined so that distant objects
might be seen clearer, or near ones magnified beyond the power of normal
vision; yet we hold with Kepler, that no instrument analogous to our
telescope was known before the early part of the 17th century.
The combination of lenses associated with the name of Galileo, was, he
tells us, of Dutch origin, and of a date anterior to that of his telescope,
Early History of the Microscope.
The instrument known as the Microscope derives its designation from two
Greek words, μικρὸς (mikros), small, and σκοπέω (skopeo), to see or
observe; and is an optical instrument by means of which objects are so
magnified that details invisible or indistinct to the naked eye are clearly
seen. Its origin, so far as yet can be traced back, seems to be of a doubtful
nature. It is tolerably certain the ancients had little or no conception of the
magnifying power of lenses; this may be surmised from their writings. The
elder Pliny incidentally states that the physicians of his day cauterised by
means of “a globe of crystal.” The learned Greek physician, Galen,
however, demonstrates conclusively that in the first and second centuries of
our era the use of magnifying lenses was quite unknown either to Greek or
Roman. Moreover, the writings of Archimedes, Ptolemy, and other learned
men, show that, although they had some idea of the action of refraction at
plane surfaces, as of water, yet of the refraction at curved surfaces they had
formed no conception. Indeed, they refer quite indiscriminately to the
spherical form, or the disc, or the plane surface of the water, but not one of
them speaks of the lenticular form, or the curvature of their surfaces.
As to the more powerful optical instruments, the telescope and microscope,
although it would appear that Alhazen in the 10th or 11th century, Roger
Bacon in the 13th, and Fracastoro and Baptist Porta in the 16th, had formed
some idea that lenses might be made and combined so that distant objects
might be seen clearer, or near ones magnified beyond the power of normal
vision; yet we hold with Kepler, that no instrument analogous to our
telescope was known before the early part of the 17th century.
The combination of lenses associated with the name of Galileo, was, he
tells us, of Dutch origin, and of a date anterior to that of his telescope,
Page 34
constructed by him in 1609; and this would appear to be the probable origin
of the microscope consisting of a combination of a convex object lens with
a concave eye lens.3
It now appears almost impossible to assign the exact date of the first
production of the microscope (as distinguished from the simple magnifying
lens), but those who have made a special investigation, agree that it must
have been invented between 1590 and 1609, and that either of the three
spectacle-makers of Middelburg, Holland, Hans Janssen, his son Zacharias
Janssen, and Hans Lippershey, may have been the inventor, the probabilities
being in favour of the Janssens, and there the question must remain.
The history of the modern microscope, like that of nations and arts, has had
its brilliant periods, in which it shone with uncommon splendour, and was
cultivated with extraordinary ardour; these periods have been succeeded by
intervals marked with no discovery, and in which the science seemed to
fade away, or at least to lie dormant, till some favourable circumstance—the
discovery of a new object, or some new improvement in the instruments of
observation—awakened the attention of the curious, and reanimated the
spirit of research. Thus, soon after the invention of the microscope, the field
it presented to observation was cultivated by men of the first rank in
science, and who enriched almost every branch of natural history by the
discoveries made by means of this instrument.
The Modern Microscope.
To the celebrated Dr. Hooke belongs the honour of publishing an account of
the compound instrument in 1665 in his “Micrographia.” His first claim,
however, is founded on the application of a lamp adjustable on a pillar,
together with a glass globe of water and a deep plano-convex condensing
lens. By means of this arrangement, he says, “The light can be directed
more directly on the object under examination.” In the further description
given of his microscope, he explains: “It has four draw-tubes for
lengthening the body, and a third lens to the optical combination.” This, it
would appear, was only brought into use when he wished to see the whole
object at once: “The middle-glass lens, conveying a very great company of
of the microscope consisting of a combination of a convex object lens with
a concave eye lens.3
It now appears almost impossible to assign the exact date of the first
production of the microscope (as distinguished from the simple magnifying
lens), but those who have made a special investigation, agree that it must
have been invented between 1590 and 1609, and that either of the three
spectacle-makers of Middelburg, Holland, Hans Janssen, his son Zacharias
Janssen, and Hans Lippershey, may have been the inventor, the probabilities
being in favour of the Janssens, and there the question must remain.
The history of the modern microscope, like that of nations and arts, has had
its brilliant periods, in which it shone with uncommon splendour, and was
cultivated with extraordinary ardour; these periods have been succeeded by
intervals marked with no discovery, and in which the science seemed to
fade away, or at least to lie dormant, till some favourable circumstance—the
discovery of a new object, or some new improvement in the instruments of
observation—awakened the attention of the curious, and reanimated the
spirit of research. Thus, soon after the invention of the microscope, the field
it presented to observation was cultivated by men of the first rank in
science, and who enriched almost every branch of natural history by the
discoveries made by means of this instrument.
The Modern Microscope.
To the celebrated Dr. Hooke belongs the honour of publishing an account of
the compound instrument in 1665 in his “Micrographia.” His first claim,
however, is founded on the application of a lamp adjustable on a pillar,
together with a glass globe of water and a deep plano-convex condensing
lens. By means of this arrangement, he says, “The light can be directed
more directly on the object under examination.” In the further description
given of his microscope, he explains: “It has four draw-tubes for
lengthening the body, and a third lens to the optical combination.” This, it
would appear, was only brought into use when he wished to see the whole
object at once: “The middle-glass lens, conveying a very great company of
Page 35
radiating pencils (of light) which would stray away; but when I had
occasion to examine the small parts of a body, I took out the middle glass
and made use of one eye-glass with the object-glass.”
From Hooke’s description I gather that he also introduced the ball-and-
socket movement into the construction of the body of his instrument. This
has found many imitators since his day; some of them have gone so far as to
claim the invention as one quite new. For small accessories, where the
leverage need not be considered, the ball-and-socket has proved convenient
enough; but not, however, if applied to the stand of the microscope. Hooke,
in his early work, expressed dissatisfaction with the English-made lenses he
had in use. He complains of the “apertures of the object-glasses, which are
so small that very few rays are admitted; none will admit a sufficient
number of rays to magnifie the object beyond a determinate bigness.” So
we may take it that he thus early discovered the great importance of an
increase in the aperture of his microscope. Other improvements of
importance were made, and he was the first to describe a useful method of
estimating the magnifying power of his lenses, and the difficulty of
distinguishing between a prominence and a depression in the object under
investigation, which he was made more fully aware of when preparing
drawings for the illustration of his “Micrographia Illustrata”; this would be
in 1664, if not earlier. His book created no little sensation on its first
appearance, and it soon became scarce. Hooke (says Mr. Mayall) “must
undoubtedly be credited with the first suggestion of immersion lenses.”
Nevertheless, in his “Lectures and Collections,” published in 1676, he
appears to be no longer enthusiastic over his double microscope, and once
more he reverts to the simpler instrument of his earlier days. Whether this
change of opinion was due to the publication of Leeuwenhoek’s
observations with his simple microscopes it is impossible to say.
As early as 1673 Leeuwenhoek communicated some important discoveries
made by a simple microscope of his own construction to the Royal Society;
he, however, gave no particulars of the construction of the instrument. Dr.
Adams, writing to his friend (Sir) Hans Sloane, says: “They appear to be
spherules lodged between two plates of gold or brass, in a hole whose
diameter appears to be no bigger than that of a small pin’s head.” At his
death he bequeathed to the Royal Society a cabinet containing twenty-six of
occasion to examine the small parts of a body, I took out the middle glass
and made use of one eye-glass with the object-glass.”
From Hooke’s description I gather that he also introduced the ball-and-
socket movement into the construction of the body of his instrument. This
has found many imitators since his day; some of them have gone so far as to
claim the invention as one quite new. For small accessories, where the
leverage need not be considered, the ball-and-socket has proved convenient
enough; but not, however, if applied to the stand of the microscope. Hooke,
in his early work, expressed dissatisfaction with the English-made lenses he
had in use. He complains of the “apertures of the object-glasses, which are
so small that very few rays are admitted; none will admit a sufficient
number of rays to magnifie the object beyond a determinate bigness.” So
we may take it that he thus early discovered the great importance of an
increase in the aperture of his microscope. Other improvements of
importance were made, and he was the first to describe a useful method of
estimating the magnifying power of his lenses, and the difficulty of
distinguishing between a prominence and a depression in the object under
investigation, which he was made more fully aware of when preparing
drawings for the illustration of his “Micrographia Illustrata”; this would be
in 1664, if not earlier. His book created no little sensation on its first
appearance, and it soon became scarce. Hooke (says Mr. Mayall) “must
undoubtedly be credited with the first suggestion of immersion lenses.”
Nevertheless, in his “Lectures and Collections,” published in 1676, he
appears to be no longer enthusiastic over his double microscope, and once
more he reverts to the simpler instrument of his earlier days. Whether this
change of opinion was due to the publication of Leeuwenhoek’s
observations with his simple microscopes it is impossible to say.
As early as 1673 Leeuwenhoek communicated some important discoveries
made by a simple microscope of his own construction to the Royal Society;
he, however, gave no particulars of the construction of the instrument. Dr.
Adams, writing to his friend (Sir) Hans Sloane, says: “They appear to be
spherules lodged between two plates of gold or brass, in a hole whose
diameter appears to be no bigger than that of a small pin’s head.” At his
death he bequeathed to the Royal Society a cabinet containing twenty-six of
Page 36
these microscopes; the cabinet and the microscopes long ago disappeared,
but not before they were carefully examined and described by Mr. Henry
Baker, F.R.S. In his report to the Royal Society, he says: “They consisted of
a series of convex-lenses, ranging in power from 1·20 to 1·5, and
magnifying from 160 to 40 diameters.” This must now be regarded as an
eventful period in the history of the microscope, since Leeuwenhoek’s
discoveries created a great sensation throughout Europe. And all further
improvements in compound instruments appear to have been laid aside for
some considerable period in consequence: and the pocket instrument of
Wilson, together with that of his scroll standard (seen on the cover of this
book), and which was one of the first simple microscopes with a mirror
mounted on the base in a line with the optic axis.
The discoveries once more made, and at a much later period (1738), by Dr.
Nathaniel Lieberkuhn with his simple microscopes, and by means of which
he discovered the minute structure of the mucous membrane of the
alimentary canal, and which alone would have immortalised his name had
we not preserved in use to this day an important adjunct of every modern
instrument, the Lieberkuhn reflector.
In the Museum of the Royal College of Surgeons of England, there is a
small cabinet of two drawers, containing a set of twelve of his simple
microscopes, each being provided with an original injection. The form of
the instrument is shown in Figs. 1 and 2. a b represents a piece of brass
tubing about an inch long and an inch in diameter and provided with a cap
at each extremity. The one at a carries a small double-convex lens of half an
inch focal length; while at b there is fixed a condensing lens three-quarters
of an inch in diameter. In Fig. 2 the instrument is seen in section, and
explains itself. It is held by the handle in such a position that the rays of
light, from a lamp or a white cloud, may fall on the condenser b, and
concentrate on the speculum l. This again further condenses the rays on the
disc c, where the object is held, and its adjustment made by the milled-head
screw d, so as to bring it within the focus of the lens a.
From this digression I pass on to the evolution of the compound
microscope. The earliest workable form known was that designed by
Eustachio Divini, who brought it to the notice of the Royal Society in 1668.
but not before they were carefully examined and described by Mr. Henry
Baker, F.R.S. In his report to the Royal Society, he says: “They consisted of
a series of convex-lenses, ranging in power from 1·20 to 1·5, and
magnifying from 160 to 40 diameters.” This must now be regarded as an
eventful period in the history of the microscope, since Leeuwenhoek’s
discoveries created a great sensation throughout Europe. And all further
improvements in compound instruments appear to have been laid aside for
some considerable period in consequence: and the pocket instrument of
Wilson, together with that of his scroll standard (seen on the cover of this
book), and which was one of the first simple microscopes with a mirror
mounted on the base in a line with the optic axis.
The discoveries once more made, and at a much later period (1738), by Dr.
Nathaniel Lieberkuhn with his simple microscopes, and by means of which
he discovered the minute structure of the mucous membrane of the
alimentary canal, and which alone would have immortalised his name had
we not preserved in use to this day an important adjunct of every modern
instrument, the Lieberkuhn reflector.
In the Museum of the Royal College of Surgeons of England, there is a
small cabinet of two drawers, containing a set of twelve of his simple
microscopes, each being provided with an original injection. The form of
the instrument is shown in Figs. 1 and 2. a b represents a piece of brass
tubing about an inch long and an inch in diameter and provided with a cap
at each extremity. The one at a carries a small double-convex lens of half an
inch focal length; while at b there is fixed a condensing lens three-quarters
of an inch in diameter. In Fig. 2 the instrument is seen in section, and
explains itself. It is held by the handle in such a position that the rays of
light, from a lamp or a white cloud, may fall on the condenser b, and
concentrate on the speculum l. This again further condenses the rays on the
disc c, where the object is held, and its adjustment made by the milled-head
screw d, so as to bring it within the focus of the lens a.
From this digression I pass on to the evolution of the compound
microscope. The earliest workable form known was that designed by
Eustachio Divini, who brought it to the notice of the Royal Society in 1668.
Page 37
It consisted of two plano-convex lenses, combined with
their convex surfaces retained in apposition. His idea was
subsequently improved upon by a London optician. Not
long afterwards, Philip Bonnani published an account of
his improved compound microscope; and we are
certainly indebted to him for two or more forms of the
movable horizontal microscopes, and for the compound
condenser fitted with focussing gear for illuminating
transparent objects by transmitted light. I must, however,
pass by the many changes made in the structure and form
of the instrument by the celebrated Dr. Culpeper, Scarlet,
Cuff, and many other inventors.
Benjamin Martin’s Microscope.—Benjamin Martin,
about 1742, was busily engaged in making improvements
in the microscope, and I may say he was certainly the
first to provide accurate results for determining the exact
magnifying power of any object-lens, so that the observer
might state the exact amplification in a certain number of
diameters. He devised numerous improvements in the
mechanism and optical arrangements of the instrument;
the rack and pinion focussing adjustments; the inclining
movements to the pillar carrying the stage; and the Fig. 1.
rectangular mechanical motions to the stage
itself. He was familiar with the principles of
achromatism, since it appears he produced an
achromatic objective about 1759, and he is said
to have sent an achromatic objective to the
Royal Society about that date. But an
ingeniously constructed microscope by Martin
found its way to George the Third, the
grandfather of our Queen, and afterwards came Fig. 2.—Lieberkuhn’s Microscope.
into the possession of the late Professor John
Quekett, of the Royal College of Surgeons, who presented it to the Royal
Microscopical Society of London. This microscope will ever associate
Martin’s name with the earliest and best form of the instrument, even
should he not receive full recognition as the inventor of the achromatic
their convex surfaces retained in apposition. His idea was
subsequently improved upon by a London optician. Not
long afterwards, Philip Bonnani published an account of
his improved compound microscope; and we are
certainly indebted to him for two or more forms of the
movable horizontal microscopes, and for the compound
condenser fitted with focussing gear for illuminating
transparent objects by transmitted light. I must, however,
pass by the many changes made in the structure and form
of the instrument by the celebrated Dr. Culpeper, Scarlet,
Cuff, and many other inventors.
Benjamin Martin’s Microscope.—Benjamin Martin,
about 1742, was busily engaged in making improvements
in the microscope, and I may say he was certainly the
first to provide accurate results for determining the exact
magnifying power of any object-lens, so that the observer
might state the exact amplification in a certain number of
diameters. He devised numerous improvements in the
mechanism and optical arrangements of the instrument;
the rack and pinion focussing adjustments; the inclining
movements to the pillar carrying the stage; and the Fig. 1.
rectangular mechanical motions to the stage
itself. He was familiar with the principles of
achromatism, since it appears he produced an
achromatic objective about 1759, and he is said
to have sent an achromatic objective to the
Royal Society about that date. But an
ingeniously constructed microscope by Martin
found its way to George the Third, the
grandfather of our Queen, and afterwards came Fig. 2.—Lieberkuhn’s Microscope.
into the possession of the late Professor John
Quekett, of the Royal College of Surgeons, who presented it to the Royal
Microscopical Society of London. This microscope will ever associate
Martin’s name with the earliest and best form of the instrument, even
should he not receive full recognition as the inventor of the achromatic
Page 38
microscope. On this account I introduce a carefully made drawing of so
singularly perfect a form of the early English microscope to the notice of
my readers. (Fig. 3.) The description given of it by the late Professor
Quekett is as follows:—“It stands about two feet in height, and is supported
on a tripod base, A; the central part of the stem, B, is of triangular figure,
having a rack at the back, upon which the stage, O, and frame, D,
supporting the mirror, E, are capable of being moved up or down. The
compound body, F, is three inches in diameter; it is composed of two tubes,
the inner of which contains the eye-piece, and can be raised or depressed by
rack and pinion, so as to increase or diminish the magnifying power. At the
base of the triangular bar is a cradle joint, G, by which the instrument can
be inclined by turning the screw-head, H (connected with an endless screw
acting upon a worm-wheel). The arm, I, supporting the compound body, is
supplied with a rack and pinion, K, by which it can be moved backwards
and forwards, and a joint is placed below it, upon which the body can be
turned into the horizontal position; another bar, carrying a stage and mirror,
can be attached by a screw, L N, so as to convert it into a horizontal
microscope. The stage, O, is provided with all the usual apparatus for
clamping objects, and a condenser can be applied to its under surface; the
stage itself may be removed, the arm, P, supporting it, turned round on the
pivot, C, and another stage of exquisite workmanship placed in its stead, the
under surface of which is shown at Q.”
This stage is strictly a micrometer one, having rectangular movements and a
fine adjustment, the movements being accomplished by the fine-threaded
screws, the milled heads of which are graduated. The mirror, E, is a double
one, and can be raised or depressed by rack and pinion; it is also capable of
removal, and an apparatus for holding large opaque objects, such as
minerals, can be substituted for it. The accessory instruments are very
numerous, and amongst the more remarkable may be mentioned a tube, M,
containing a speculum, which can take the place of the tube, R, and so form
a reflecting microscope. The apparatus for holding animalcules or other live
objects, which is represented at S, as well as a plate of glass six inches in
diameter, with four concave wells ground in it, can be applied to the stage,
so that each well may be brought in succession under the magnifying
power. The lenses belonging to this microscope are twenty-four in number;
they vary in focal length from four inches to one-tenth of an inch; ten of
singularly perfect a form of the early English microscope to the notice of
my readers. (Fig. 3.) The description given of it by the late Professor
Quekett is as follows:—“It stands about two feet in height, and is supported
on a tripod base, A; the central part of the stem, B, is of triangular figure,
having a rack at the back, upon which the stage, O, and frame, D,
supporting the mirror, E, are capable of being moved up or down. The
compound body, F, is three inches in diameter; it is composed of two tubes,
the inner of which contains the eye-piece, and can be raised or depressed by
rack and pinion, so as to increase or diminish the magnifying power. At the
base of the triangular bar is a cradle joint, G, by which the instrument can
be inclined by turning the screw-head, H (connected with an endless screw
acting upon a worm-wheel). The arm, I, supporting the compound body, is
supplied with a rack and pinion, K, by which it can be moved backwards
and forwards, and a joint is placed below it, upon which the body can be
turned into the horizontal position; another bar, carrying a stage and mirror,
can be attached by a screw, L N, so as to convert it into a horizontal
microscope. The stage, O, is provided with all the usual apparatus for
clamping objects, and a condenser can be applied to its under surface; the
stage itself may be removed, the arm, P, supporting it, turned round on the
pivot, C, and another stage of exquisite workmanship placed in its stead, the
under surface of which is shown at Q.”
This stage is strictly a micrometer one, having rectangular movements and a
fine adjustment, the movements being accomplished by the fine-threaded
screws, the milled heads of which are graduated. The mirror, E, is a double
one, and can be raised or depressed by rack and pinion; it is also capable of
removal, and an apparatus for holding large opaque objects, such as
minerals, can be substituted for it. The accessory instruments are very
numerous, and amongst the more remarkable may be mentioned a tube, M,
containing a speculum, which can take the place of the tube, R, and so form
a reflecting microscope. The apparatus for holding animalcules or other live
objects, which is represented at S, as well as a plate of glass six inches in
diameter, with four concave wells ground in it, can be applied to the stage,
so that each well may be brought in succession under the magnifying
power. The lenses belonging to this microscope are twenty-four in number;
they vary in focal length from four inches to one-tenth of an inch; ten of
Page 39
them are supplied with Lieberkuhns. A
small arm, capable of carrying single
lenses, can be supplied at T, and when
turned over, the stage of the instrument
becomes a single microscope; there are
four lenses suitable for this purpose,
their focal length varying from one-
tenth to one-fortieth of an inch. The
performance of all the lenses is
excellent, and no pains appear to have
been spared in their construction. There
are numerous other pieces of accessory
apparatus, all remarkable for the beauty
of their workmanship.4
In addition to the movements described
by Quekett, the body-tube with its
support can be moved in an arc
concentrically with the axis of the
triangular pillar, on the top of which it
is fitted with a worm-wheel and
endless-screw mechanism, actuated by
Fig. 3.—Martin’s Universal Microscope. 1782. the screw-head, T, below. It must
therefore be admitted that Martin led
the way far beyond his contemporaries, both in the design and the evolution
of the microscope. Furthermore, in his “New Elements of Optics,” 1759, he
dealt with the principle of achromatism, by the construction of an
achromatic telescope.
At a somewhat later period there lived in London a philosophical
instrument maker of some repute, George Adams, who published in 1746 a
quarto book, entitled “Micrographia Illustrata, or the Knowledge of the
Microscope Explained.” This work fairly well describes “the nature, uses,
and magnifying powers of microscopes in general, together with full
directions how to prepare, apply, examine, and preserve minute objects.”
Adams’ book was the first of the kind published in this country, and it
contributed in no small degree to the advancement of microscopical
small arm, capable of carrying single
lenses, can be supplied at T, and when
turned over, the stage of the instrument
becomes a single microscope; there are
four lenses suitable for this purpose,
their focal length varying from one-
tenth to one-fortieth of an inch. The
performance of all the lenses is
excellent, and no pains appear to have
been spared in their construction. There
are numerous other pieces of accessory
apparatus, all remarkable for the beauty
of their workmanship.4
In addition to the movements described
by Quekett, the body-tube with its
support can be moved in an arc
concentrically with the axis of the
triangular pillar, on the top of which it
is fitted with a worm-wheel and
endless-screw mechanism, actuated by
Fig. 3.—Martin’s Universal Microscope. 1782. the screw-head, T, below. It must
therefore be admitted that Martin led
the way far beyond his contemporaries, both in the design and the evolution
of the microscope. Furthermore, in his “New Elements of Optics,” 1759, he
dealt with the principle of achromatism, by the construction of an
achromatic telescope.
At a somewhat later period there lived in London a philosophical
instrument maker of some repute, George Adams, who published in 1746 a
quarto book, entitled “Micrographia Illustrata, or the Knowledge of the
Microscope Explained.” This work fairly well describes “the nature, uses,
and magnifying powers of microscopes in general, together with full
directions how to prepare, apply, examine, and preserve minute objects.”
Adams’ book was the first of the kind published in this country, and it
contributed in no small degree to the advancement of microscopical
Page 40
science. Adams writes: “We owe the construction of the variable
microscope to the ingenuity and generosity of a noble person. The apparatus
belonging to it is more convenient, more certain, and more extensive than
that of any other at present extant; consequently, the advantage and pleasure
attending the observations in viewing objects through it must be as
extensive in proportion.” This is believed to apply to Martin’s several
microscopes, and that especially constructed for the king, afterwards
improved upon by Adams. Another early form of microscope, Wilson
Simple Scroll (1746), stamped on the cover of this book, and has thus
become familiar to microscopists, was also made by Adams.
We now closely approach a period fertile in the improvement of the
microscope, and in the discoveries made by its agency. The chief of those
among the honoured names of the time we find Trembley, Ellis, Baker,
Adams, Hill, Swammerdam, Lyonet, Needham, and a few others. Adams
somewhat sarcastically observes “that every optician exercises his talents in
improving (as he calls it) the microscope, in other words, in varying its
construction and rendering it different in form from that sold by his
neighbour; or at the best rendering it more complex and troublesome to
manage.” There were no doubt good reasons for these and other strictures
upon inventors as well as makers of microscopes, even in the Adams’ day.
In the year 1787 the “Microscopical Essays” of his son were published, in
which he described all the instruments in use up to that period.
Looking back, and taking a general survey of the work of nearly two
centuries in the history of the microscope, it cannot be said that either in its
optical or mechanical construction any great amount of progress was made.
This in part may have arisen from the fact that no pressing need was felt for
either delicate focussing or higher magnification. At all events, it was not
until the application of achromatism to the instrument that new life was
infused into its use, and a great impetus was given to its development, both
optically and mechanically.
In the year 1823 a strong desire became manifest for improved forms of the
instrument, in France by M. Selligue, by Frauenhofer in Munich, by Amici
in Modena, by M. Chevalier in Paris, and by Dr. Goring, Mr. Pritchard, and
Mr. Tully in London. The result was that in 1824 a new form of achromatic
microscope to the ingenuity and generosity of a noble person. The apparatus
belonging to it is more convenient, more certain, and more extensive than
that of any other at present extant; consequently, the advantage and pleasure
attending the observations in viewing objects through it must be as
extensive in proportion.” This is believed to apply to Martin’s several
microscopes, and that especially constructed for the king, afterwards
improved upon by Adams. Another early form of microscope, Wilson
Simple Scroll (1746), stamped on the cover of this book, and has thus
become familiar to microscopists, was also made by Adams.
We now closely approach a period fertile in the improvement of the
microscope, and in the discoveries made by its agency. The chief of those
among the honoured names of the time we find Trembley, Ellis, Baker,
Adams, Hill, Swammerdam, Lyonet, Needham, and a few others. Adams
somewhat sarcastically observes “that every optician exercises his talents in
improving (as he calls it) the microscope, in other words, in varying its
construction and rendering it different in form from that sold by his
neighbour; or at the best rendering it more complex and troublesome to
manage.” There were no doubt good reasons for these and other strictures
upon inventors as well as makers of microscopes, even in the Adams’ day.
In the year 1787 the “Microscopical Essays” of his son were published, in
which he described all the instruments in use up to that period.
Looking back, and taking a general survey of the work of nearly two
centuries in the history of the microscope, it cannot be said that either in its
optical or mechanical construction any great amount of progress was made.
This in part may have arisen from the fact that no pressing need was felt for
either delicate focussing or higher magnification. At all events, it was not
until the application of achromatism to the instrument that new life was
infused into its use, and a great impetus was given to its development, both
optically and mechanically.
In the year 1823 a strong desire became manifest for improved forms of the
instrument, in France by M. Selligue, by Frauenhofer in Munich, by Amici
in Modena, by M. Chevalier in Paris, and by Dr. Goring, Mr. Pritchard, and
Mr. Tully in London. The result was that in 1824 a new form of achromatic
Page 41
object-glass was constructed of nine-tenths of an inch focal length,
composed of three lenses, and transmitting a pencil of eighteen degrees; and
which, as regards accurate correction throughout the field, was for some
years regarded as perfect.
Sir David Brewster was the first to suggest the great importance of
introducing materials of a more highly refracting nature into the
construction of lenses. He wrote: “There can be no essential improvement
expected in the microscope unless from the discovery of some transparent
substance which, like the diamond, combines a high refractive with a low
dispersive power.” Having experienced the greatest difficulty in getting a
small diamond cut into a prism in London, he did not conceive it
practicable to grind, polish, and form it into a lens.
Mr. Pritchard, however, was led to make the experiment, and on the 1st of
December, 1824, “he had the pleasure of first looking through a diamond
microscope.” Dr. Goring also tried its performance on various objects, both
as a single microscope and as an objective of a compound instrument, and
satisfied himself of its superiority over other kinds of lenses. But here Mr.
Pritchard’s labours did not end. He subsequently found that the diamond
used had many flaws in it, which led him to abandon the idea of finishing it.
Having been prevented from resuming his operations on this refractory
material for a time he made a third attempt, and met with another
unexpected defect; he found that some lenses, unlike the first, gave a double
or triple image instead of a single one, in consequence of some of their parts
being either harder or softer than others. These defects were found to be due
to polarisation. Mr. Pritchard having learned how to decide whether a
diamond is fit for a magnifier or not, subsequently succeeded in making two
planoconvex lenses of adamant; these proved to be perfect for microscopic
purposes. “One of these, of one-twentieth of an inch in focal length, is now
in the possession of his Grace the Duke of Buckingham; the other, of one-
thirtieth of an inch focus, is in his own hands.”
“In consequence of the high refracting power of a diamond lens over a glass
lens, the former material may be at least one-third as thin as that of the
latter, and if the focal length of both be equal, say, one-eightieth of an inch,
the magnifying power of the diamond lens will be 2,133 diameters, whereas
composed of three lenses, and transmitting a pencil of eighteen degrees; and
which, as regards accurate correction throughout the field, was for some
years regarded as perfect.
Sir David Brewster was the first to suggest the great importance of
introducing materials of a more highly refracting nature into the
construction of lenses. He wrote: “There can be no essential improvement
expected in the microscope unless from the discovery of some transparent
substance which, like the diamond, combines a high refractive with a low
dispersive power.” Having experienced the greatest difficulty in getting a
small diamond cut into a prism in London, he did not conceive it
practicable to grind, polish, and form it into a lens.
Mr. Pritchard, however, was led to make the experiment, and on the 1st of
December, 1824, “he had the pleasure of first looking through a diamond
microscope.” Dr. Goring also tried its performance on various objects, both
as a single microscope and as an objective of a compound instrument, and
satisfied himself of its superiority over other kinds of lenses. But here Mr.
Pritchard’s labours did not end. He subsequently found that the diamond
used had many flaws in it, which led him to abandon the idea of finishing it.
Having been prevented from resuming his operations on this refractory
material for a time he made a third attempt, and met with another
unexpected defect; he found that some lenses, unlike the first, gave a double
or triple image instead of a single one, in consequence of some of their parts
being either harder or softer than others. These defects were found to be due
to polarisation. Mr. Pritchard having learned how to decide whether a
diamond is fit for a magnifier or not, subsequently succeeded in making two
planoconvex lenses of adamant; these proved to be perfect for microscopic
purposes. “One of these, of one-twentieth of an inch in focal length, is now
in the possession of his Grace the Duke of Buckingham; the other, of one-
thirtieth of an inch focus, is in his own hands.”
“In consequence of the high refracting power of a diamond lens over a glass
lens, the former material may be at least one-third as thin as that of the
latter, and if the focal length of both be equal, say, one-eightieth of an inch,
the magnifying power of the diamond lens will be 2,133 diameters, whereas
Page 42
that of glass will be only 800.” At a date (1812) before Brewster proposed
diamond lenses he demonstrated a simple method of rendering both single
and compound microscopes achromatic. “Starting,” he says, “with the
principle that all objects, however delicate, are best seen when immersed in
fluid, he placed an object on a slip of glass, and put above a drop of oil,
having a greater dispersive power than the single concave lens, which
formed the object-glass of the microscope. The lens was then made to touch
the fluid, so that the surface of the fluid was formed into a concave lens,
and if the radius of the outward surface was such as to correct the
dispersion, we should have a perfect achromatic microscope.” Here we
have the immersion system foreshadowed. Shortly after these experiments
of Brewster’s were in progress, Dr. Goring is said to have discovered that
the structure of certain bodies could be readily seen in some microscopes
and not in others. These bodies he named test objects. He then examined
these tests with the achromatic combinations of the Tullys, and was led to
the discovery that “the penetrating power of the microscope depends upon
its angle of aperture.”
“While these practical investigations were in progress,” writes Andrew
Ross, “the subject of achromatism engaged the attention of some of the
most profound mathematicians in England, Sir John Herschel, and
Professors Airy and Barlow. Mr. Coddington and others contributed largely
to the theoretical examination of the subject; and although the results of
their labours were not applicable to the microscope, they essentially
promoted its improvement.”
About this period (1812) Professor Amici, of Modena, was experimentally
engaged in the improvement of the achromatic object-glass, and he invented
a reflecting microscope superior to those of Newton, Baker, or Smith, made
as early as 1738, and long ago abandoned. In 1815 Amici made further
experiments, and introduced the immersion system; while Frauenhofer, of
Munich, about the same time constructed object-glasses for the microscope
of a single achromatic lens, in which the two glasses, although placed in
juxtaposition, were not cemented together.
Dolland, it has been said, introduced achromatic lenses; but although he
constructed many achromatic telescopes, he did not apply the same
diamond lenses he demonstrated a simple method of rendering both single
and compound microscopes achromatic. “Starting,” he says, “with the
principle that all objects, however delicate, are best seen when immersed in
fluid, he placed an object on a slip of glass, and put above a drop of oil,
having a greater dispersive power than the single concave lens, which
formed the object-glass of the microscope. The lens was then made to touch
the fluid, so that the surface of the fluid was formed into a concave lens,
and if the radius of the outward surface was such as to correct the
dispersion, we should have a perfect achromatic microscope.” Here we
have the immersion system foreshadowed. Shortly after these experiments
of Brewster’s were in progress, Dr. Goring is said to have discovered that
the structure of certain bodies could be readily seen in some microscopes
and not in others. These bodies he named test objects. He then examined
these tests with the achromatic combinations of the Tullys, and was led to
the discovery that “the penetrating power of the microscope depends upon
its angle of aperture.”
“While these practical investigations were in progress,” writes Andrew
Ross, “the subject of achromatism engaged the attention of some of the
most profound mathematicians in England, Sir John Herschel, and
Professors Airy and Barlow. Mr. Coddington and others contributed largely
to the theoretical examination of the subject; and although the results of
their labours were not applicable to the microscope, they essentially
promoted its improvement.”
About this period (1812) Professor Amici, of Modena, was experimentally
engaged in the improvement of the achromatic object-glass, and he invented
a reflecting microscope superior to those of Newton, Baker, or Smith, made
as early as 1738, and long ago abandoned. In 1815 Amici made further
experiments, and introduced the immersion system; while Frauenhofer, of
Munich, about the same time constructed object-glasses for the microscope
of a single achromatic lens, in which the two glasses, although placed in
juxtaposition, were not cemented together.
Dolland, it has been said, introduced achromatic lenses; but although he
constructed many achromatic telescopes, he did not apply the same
Page 43
principle to microscopes, and those which he sold were only modifications
of the compound microscope of Cuff.
Dr. Wollaston employed a new form of combination in a microscope
constructed for his own use, and by which “he was able to see distinctly the
finest markings upon the scales of the Lepisma and Podura, and upon those
of the gnat’s wing.” His doublet is still employed, and to which I shall refer
under “Simple Microscopes.”
Fig. 3a.—Sir David Brewster’s Microscope, of the early part of the century,
recently presented to the British Museum.
of the compound microscope of Cuff.
Dr. Wollaston employed a new form of combination in a microscope
constructed for his own use, and by which “he was able to see distinctly the
finest markings upon the scales of the Lepisma and Podura, and upon those
of the gnat’s wing.” His doublet is still employed, and to which I shall refer
under “Simple Microscopes.”
Fig. 3a.—Sir David Brewster’s Microscope, of the early part of the century,
recently presented to the British Museum.
Page 44
CHAPTER I.
Elementary Optics.
Value of Inductive Science—Light: Its Propagation, Refraction, Reflection
—Spherical and Chromatic Aberrations—Human Eye, formation of
Images of External Objects in—Visual Angle increased—Abbe’s
Theory of Microscopic Vision.
The advances made in physics and mechanics during the 17th and 18th
centuries fairly opened the way to the attainment of greater perfection in all
optical instruments. This has been particularly exemplified with reference to
the invention of the microscope, as briefly sketched out in the previous
chapter. Indeed, in the first half of the present century the microscope can
scarcely be said to have held a position of importance among the scientific
instruments in frequent use. Since then, however, the zoologist and botanist
by its aid have laid bare the intimate structure of plants and animals, and
thereby have opened up a vast kingdom of minute forms of life previously
undreamt of; and in connection with chemistry a new science has been
founded, that of bacteriology.
For these reasons it will be of importance to the student of microscopy to
begin at the beginning, and it will be my endeavour to introduce to his
notice such facts in physical optics as are closely associated with the
formation of images, and, so to speak, systematise such stepping stones for
work hereafter to be accomplished. Elementary principles only will be
adduced, and without attempting to involve my readers in intricate
mathematical problems, and which for the most part are unnecessary for the
attainment of the object in view. I therefore pass at once to the consideration
of the propagation of light through certain bodies.
Elementary Optics.
Value of Inductive Science—Light: Its Propagation, Refraction, Reflection
—Spherical and Chromatic Aberrations—Human Eye, formation of
Images of External Objects in—Visual Angle increased—Abbe’s
Theory of Microscopic Vision.
The advances made in physics and mechanics during the 17th and 18th
centuries fairly opened the way to the attainment of greater perfection in all
optical instruments. This has been particularly exemplified with reference to
the invention of the microscope, as briefly sketched out in the previous
chapter. Indeed, in the first half of the present century the microscope can
scarcely be said to have held a position of importance among the scientific
instruments in frequent use. Since then, however, the zoologist and botanist
by its aid have laid bare the intimate structure of plants and animals, and
thereby have opened up a vast kingdom of minute forms of life previously
undreamt of; and in connection with chemistry a new science has been
founded, that of bacteriology.
For these reasons it will be of importance to the student of microscopy to
begin at the beginning, and it will be my endeavour to introduce to his
notice such facts in physical optics as are closely associated with the
formation of images, and, so to speak, systematise such stepping stones for
work hereafter to be accomplished. Elementary principles only will be
adduced, and without attempting to involve my readers in intricate
mathematical problems, and which for the most part are unnecessary for the
attainment of the object in view. I therefore pass at once to the consideration
of the propagation of light through certain bodies.
Page 45
The microscope, whether simple or compound, depends for its magnifying
power on the influence exerted by lenses in altering the course of the rays
of light passing through them being REFRACTED. Refraction takes place in
accordance with two well-known laws of optics. When a ray of light passes
from one transparent medium to another it undergoes a change of direction
at the surface of separation, so that its course in the second medium makes
an angle with its course in the first. This change of direction is a resultant of
refraction. The broken appearance presented by a stick partly immersed in
water, and viewed in an oblique position, is an illustration of the law of
refraction. Liquids have a greater refractive power than air or gases. As a
rule, with some few exceptions, the denser of the two substances has the
greater refractive power; hence it is customary in enumerating some of the
laws of optics to speak of the denser medium and the rarer medium. The
more correct designation would be the more refractive and the less
refractive.5
Let R I (Fig. 4) be a ray
incident at I on the surface of
separation of two media, and
let I S′ be the course of the ray
after refraction. Then the
angles which R I and I S make
with the normal are the angle
of incidence and the angle of
refraction respectively, and the
first law of refraction is that
these angles lie in the same
plane, or the plane of
refraction is the same as the
plane of incidence. The law
which connects the magnitudes
of these angles, and which was
discovered by Snell, a Dutch Fig. 4.—Law of Refraction.
philosopher, can only be stated
either by reference to a geometrical construction, or by using the language
of trigonometry. Describe a circle about the point of incidence, I as a centre,
and drop perpendiculars from the points where it cuts the rays on the
power on the influence exerted by lenses in altering the course of the rays
of light passing through them being REFRACTED. Refraction takes place in
accordance with two well-known laws of optics. When a ray of light passes
from one transparent medium to another it undergoes a change of direction
at the surface of separation, so that its course in the second medium makes
an angle with its course in the first. This change of direction is a resultant of
refraction. The broken appearance presented by a stick partly immersed in
water, and viewed in an oblique position, is an illustration of the law of
refraction. Liquids have a greater refractive power than air or gases. As a
rule, with some few exceptions, the denser of the two substances has the
greater refractive power; hence it is customary in enumerating some of the
laws of optics to speak of the denser medium and the rarer medium. The
more correct designation would be the more refractive and the less
refractive.5
Let R I (Fig. 4) be a ray
incident at I on the surface of
separation of two media, and
let I S′ be the course of the ray
after refraction. Then the
angles which R I and I S make
with the normal are the angle
of incidence and the angle of
refraction respectively, and the
first law of refraction is that
these angles lie in the same
plane, or the plane of
refraction is the same as the
plane of incidence. The law
which connects the magnitudes
of these angles, and which was
discovered by Snell, a Dutch Fig. 4.—Law of Refraction.
philosopher, can only be stated
either by reference to a geometrical construction, or by using the language
of trigonometry. Describe a circle about the point of incidence, I as a centre,
and drop perpendiculars from the points where it cuts the rays on the
Page 46
normal. The law is that these perpendiculars, R′ P′, S′ P, will have a constant
ratio, or the sines of the angles of incidence and refraction are in a constant
ratio; that is, so long as the media through which the ray first passes, and by
which it is afterwards refracted, remain the same, and the light also of the
same kind, then it is referred to as the law of sines.
Indices of Refraction.
The ratio of the sine of the angle of incidence to the sine of the angle of
refraction, when a ray passes from one medium to another is termed the
relative index of refraction. When a ray passes from vacuum into any
medium, this ratio is always greater than unity, and is called the absolute
index of refraction, or simply the index of refraction for the medium in
question.
The absolute index of air is so small that it may be neglected in comparison
with those of solids and liquids; but strictly speaking, the relative index for
a ray passing from air into a given substance must be multiplied by the
absolute index of the air, in order to obtain the true index of refraction.
Critical Angle.—It will be seen
from the law of sines that, when the
incident ray is in the less refractive
of the two media, to every possible
angle of incidence there is a
corresponding angle of refraction.
The angle referred to is termed the
critical angle, and is readily
computed if the relative index of
Fig. 5.—Vision through a Glass Plate. refraction be given. When the media
are air and water, this angle is about
48° 30′. For air and ordinary kinds of glass its value varies from 38° to 41°.
The phenomenon of total reflection may be observed in several familiar
instances. For example, if a glass of water, with a spoon in it, is held above
the level of the eye, the under side of the surface is seen to shine like a
ratio, or the sines of the angles of incidence and refraction are in a constant
ratio; that is, so long as the media through which the ray first passes, and by
which it is afterwards refracted, remain the same, and the light also of the
same kind, then it is referred to as the law of sines.
Indices of Refraction.
The ratio of the sine of the angle of incidence to the sine of the angle of
refraction, when a ray passes from one medium to another is termed the
relative index of refraction. When a ray passes from vacuum into any
medium, this ratio is always greater than unity, and is called the absolute
index of refraction, or simply the index of refraction for the medium in
question.
The absolute index of air is so small that it may be neglected in comparison
with those of solids and liquids; but strictly speaking, the relative index for
a ray passing from air into a given substance must be multiplied by the
absolute index of the air, in order to obtain the true index of refraction.
Critical Angle.—It will be seen
from the law of sines that, when the
incident ray is in the less refractive
of the two media, to every possible
angle of incidence there is a
corresponding angle of refraction.
The angle referred to is termed the
critical angle, and is readily
computed if the relative index of
Fig. 5.—Vision through a Glass Plate. refraction be given. When the media
are air and water, this angle is about
48° 30′. For air and ordinary kinds of glass its value varies from 38° to 41°.
The phenomenon of total reflection may be observed in several familiar
instances. For example, if a glass of water, with a spoon in it, is held above
the level of the eye, the under side of the surface is seen to shine like a
Page 47
mirror, and the lower part of the spoon is seen reflected in it. Effects of the
same kind are observed when a ray of sunlight passes into an aquarium—on
the other hand rays falling normally on a uniform transparent plate of glass
with parallel faces keep their course; but objects viewed obliquely through
the same are displaced from their true position. Let S (Fig. 5) be a luminous
point which sends light to an eye not directly opposite to it, on the other
side of a parallel plate. The emergent rays which enter the eye are parallel to
the incident rays; but as they have undergone lateral displacement, their
point of concourse is changed from S to S′, and this is accordingly the
image of S. The rays in such a case which compose the pencil that enters
the eye will not exactly meet in any one point; there will be two focal lines,
just as in the case of spherical mirrors. The displacement produced, as seen
in the figure referred to above, increases with the thickness of the plate, its
index of refraction, and the obliquity of incidence. This furnishes one of the
simplest means of measuring the index of refraction of a glass substance,
and is thus employed in Pichot’s refractometer (“Deschanel”).
Refraction through a Prism.—A
prism is a portion of a refracting
medium bounded by two plane
surfaces, inclined at a definite angle
to one another. The two plane
surfaces are termed the faces of the
prism, and their inclination to one
another is the refracting angle of the
prism. A prism preserves the
property of bending rays of light
from their original course by Fig. 6.—Refraction through a Prism.
refraction. A cylinder may be
regarded as the limit of a prism whose sides increase in number and
diminish in size indefinitely: it may also be regarded as a pyramid whose
apex is removed to an indefinite distance.
Let S I (Fig. 6) be an incident ray in the plane of the principal section of the
prism. If the external medium be air, or other substance of less refractive
power than the prism, the ray on entering the same will be bent nearer to the
normal, taking such a course as I E, and on leaving the prism will be bent
same kind are observed when a ray of sunlight passes into an aquarium—on
the other hand rays falling normally on a uniform transparent plate of glass
with parallel faces keep their course; but objects viewed obliquely through
the same are displaced from their true position. Let S (Fig. 5) be a luminous
point which sends light to an eye not directly opposite to it, on the other
side of a parallel plate. The emergent rays which enter the eye are parallel to
the incident rays; but as they have undergone lateral displacement, their
point of concourse is changed from S to S′, and this is accordingly the
image of S. The rays in such a case which compose the pencil that enters
the eye will not exactly meet in any one point; there will be two focal lines,
just as in the case of spherical mirrors. The displacement produced, as seen
in the figure referred to above, increases with the thickness of the plate, its
index of refraction, and the obliquity of incidence. This furnishes one of the
simplest means of measuring the index of refraction of a glass substance,
and is thus employed in Pichot’s refractometer (“Deschanel”).
Refraction through a Prism.—A
prism is a portion of a refracting
medium bounded by two plane
surfaces, inclined at a definite angle
to one another. The two plane
surfaces are termed the faces of the
prism, and their inclination to one
another is the refracting angle of the
prism. A prism preserves the
property of bending rays of light
from their original course by Fig. 6.—Refraction through a Prism.
refraction. A cylinder may be
regarded as the limit of a prism whose sides increase in number and
diminish in size indefinitely: it may also be regarded as a pyramid whose
apex is removed to an indefinite distance.
Let S I (Fig. 6) be an incident ray in the plane of the principal section of the
prism. If the external medium be air, or other substance of less refractive
power than the prism, the ray on entering the same will be bent nearer to the
normal, taking such a course as I E, and on leaving the prism will be bent
Page 48
away from the normal, taking the course E B. The effect of these two
refractions is, therefore, to turn the ray away from the edge (or refracting
angle) of the prism. In practice, the prism is usually so placed that I E, the
path of the ray through the prism, makes equal angles with the two faces at
which refraction occurs. If the prism is turned very far from this position,
the course of the ray may be altogether different from that represented in
the figure; it may enter at one face, be internally reflected at another, and
come out at the third.
It is evident, therefore, that the minimum number of sides, i.e., the
bounding faces, exclusive of the ends, which a prism can have is three. In
this form, it constitutes a most valuable instrument of research in physical
optics. A convex lens is practically merely a curved form of two prisms
combined, their bases being brought into contact; on the other hand the
concave lens is simply a reversal of the position of the apices brought into
contact, as shown in Fig. 11. Both convex and concave lenses are therefore
closely related to the prism.
Reflection.—The laws that govern the change of direction which a ray of
light experiences when it strikes upon the surfaces of separation of two
media and is thrown back into the same medium from which it approached
is as follows:—When the reflecting surface is plain the direction of the
reflected ray makes with the normal to the surface the same angle which the
incident ray makes with the same normal; or, as it is usually expressed, the
angles of reflection and incidence are equal. When the surfaces are curved
the same law holds good. In all cases of reflection the energy of the ray is
diminished, so that reflection must always be accompanied by absorption.
The latter probably precedes the former. Most bodies are visible by light
reflected from their surfaces, but before this takes place the light has
undergone a modification, namely, that which imparts colour peculiar to the
bodies viewed. When light impinges upon the surface of a denser medium
part is reflected, part absorbed, and part refracted. But for a certain angle
depending upon the refractive index of the refracting medium no refraction
takes place. This angle is termed the angle of total reflection, since all the
light which is not absorbed is wholly reflected.
refractions is, therefore, to turn the ray away from the edge (or refracting
angle) of the prism. In practice, the prism is usually so placed that I E, the
path of the ray through the prism, makes equal angles with the two faces at
which refraction occurs. If the prism is turned very far from this position,
the course of the ray may be altogether different from that represented in
the figure; it may enter at one face, be internally reflected at another, and
come out at the third.
It is evident, therefore, that the minimum number of sides, i.e., the
bounding faces, exclusive of the ends, which a prism can have is three. In
this form, it constitutes a most valuable instrument of research in physical
optics. A convex lens is practically merely a curved form of two prisms
combined, their bases being brought into contact; on the other hand the
concave lens is simply a reversal of the position of the apices brought into
contact, as shown in Fig. 11. Both convex and concave lenses are therefore
closely related to the prism.
Reflection.—The laws that govern the change of direction which a ray of
light experiences when it strikes upon the surfaces of separation of two
media and is thrown back into the same medium from which it approached
is as follows:—When the reflecting surface is plain the direction of the
reflected ray makes with the normal to the surface the same angle which the
incident ray makes with the same normal; or, as it is usually expressed, the
angles of reflection and incidence are equal. When the surfaces are curved
the same law holds good. In all cases of reflection the energy of the ray is
diminished, so that reflection must always be accompanied by absorption.
The latter probably precedes the former. Most bodies are visible by light
reflected from their surfaces, but before this takes place the light has
undergone a modification, namely, that which imparts colour peculiar to the
bodies viewed. When light impinges upon the surface of a denser medium
part is reflected, part absorbed, and part refracted. But for a certain angle
depending upon the refractive index of the refracting medium no refraction
takes place. This angle is termed the angle of total reflection, since all the
light which is not absorbed is wholly reflected.
Page 49
Multiple images are produced by a transparent parallel plate of glass. If the
glass be silvered at the back, as it usually is in the microscope-mirror, the
second image is brighter than the first, but as the angle of incidence
increases the first image gains upon the second; and if the luminous object
be a lamp or candle, a number of images, one behind the other, will be
visible to an eye properly placed in front. This is due to the fact that the
reflecting power of a surface of glass increases with the angle of incidence.
Fig. 7.—Conjugate Foci of Curved Surfaces.
Concave Surfaces.—Rays of light proceeding from any given point in
front of a concave spherical mirror, are reflected so as to meet in another
point, and the line joining the two points passes through the centre of the
sphere. The relation between them is or should be mutual, hence they are
termed conjugate foci. By a focus in general is meant a point in which a
number of rays of light meet, and the rays which thus meet, taken
collectively, are termed a pencil. Fig. 7 represents two pencils of rays
whose foci, S s, are conjugate, so that, if either of them be regarded as an
incident pencil, the other will be the corresponding reflected pencil. Each
point, in fact, sends a pencil of rays which converge, after reflection, to the
conjugate focus. The principal focal distance is half the radius of curvature.
But it will not escape attention that concave mirrors have two reflecting
surfaces, a front and a back. This, however, does not practically disturb its
virtual focus, since the achromatic condenser when brought into use collects
and concentrates the light received from the mirror upon an object for the
purpose of rendering it more distinctly visible to the eye when viewing an
glass be silvered at the back, as it usually is in the microscope-mirror, the
second image is brighter than the first, but as the angle of incidence
increases the first image gains upon the second; and if the luminous object
be a lamp or candle, a number of images, one behind the other, will be
visible to an eye properly placed in front. This is due to the fact that the
reflecting power of a surface of glass increases with the angle of incidence.
Fig. 7.—Conjugate Foci of Curved Surfaces.
Concave Surfaces.—Rays of light proceeding from any given point in
front of a concave spherical mirror, are reflected so as to meet in another
point, and the line joining the two points passes through the centre of the
sphere. The relation between them is or should be mutual, hence they are
termed conjugate foci. By a focus in general is meant a point in which a
number of rays of light meet, and the rays which thus meet, taken
collectively, are termed a pencil. Fig. 7 represents two pencils of rays
whose foci, S s, are conjugate, so that, if either of them be regarded as an
incident pencil, the other will be the corresponding reflected pencil. Each
point, in fact, sends a pencil of rays which converge, after reflection, to the
conjugate focus. The principal focal distance is half the radius of curvature.
But it will not escape attention that concave mirrors have two reflecting
surfaces, a front and a back. This, however, does not practically disturb its
virtual focus, since the achromatic condenser when brought into use collects
and concentrates the light received from the mirror upon an object for the
purpose of rendering it more distinctly visible to the eye when viewing an
Page 50
object placed on the stage of the microscope. The images seen in a plane
mirror are always virtual, and any spherical mirror, whether concave or
convex, is nearly equivalent to a plane mirror when the distance of the
object from its surface is small in comparison with the radius of curvature.
Lenses.
Forms of Lenses.—A lens is a portion of a refracting medium bounded by
two surfaces which are portions of spheres, having a common axis, termed
the axis of the lens. Lenses are distinguished by different names, according
to the nature of their surfaces.
Lenses with sharp edges (thicker at
the centre) are convergent or positive
lenses. Lenses with blunt edges
(thinner at the centre) are divergent
or negative lenses. The first group
comprises:—(1) The bi-convex lens;
(2) the plano-convex lens; (3) the
Fig. 8.—Converging and Diverging Lenses. convergent meniscus. The second
group:—(4) The concave lens; (5)
the plano-concave lens; (6) the divergent meniscus (Fig. 8).
Principal Focus.—A lens is usually a solid of revolution, and the axis of
revolution is termed the principal axis of the lens. When the surfaces are
spherical it is the line joining the centre of curvature.
From the great importance of lenses, especially convex lenses, in practical
optics, it will be necessary to explain their properties somewhat at length.
mirror are always virtual, and any spherical mirror, whether concave or
convex, is nearly equivalent to a plane mirror when the distance of the
object from its surface is small in comparison with the radius of curvature.
Lenses.
Forms of Lenses.—A lens is a portion of a refracting medium bounded by
two surfaces which are portions of spheres, having a common axis, termed
the axis of the lens. Lenses are distinguished by different names, according
to the nature of their surfaces.
Lenses with sharp edges (thicker at
the centre) are convergent or positive
lenses. Lenses with blunt edges
(thinner at the centre) are divergent
or negative lenses. The first group
comprises:—(1) The bi-convex lens;
(2) the plano-convex lens; (3) the
Fig. 8.—Converging and Diverging Lenses. convergent meniscus. The second
group:—(4) The concave lens; (5)
the plano-concave lens; (6) the divergent meniscus (Fig. 8).
Principal Focus.—A lens is usually a solid of revolution, and the axis of
revolution is termed the principal axis of the lens. When the surfaces are
spherical it is the line joining the centre of curvature.
From the great importance of lenses, especially convex lenses, in practical
optics, it will be necessary to explain their properties somewhat at length.
Page 51
Fig. 9.—Principal Focus of a Convex Lens.
Principal Focus of Convex Lens.—When rays which were originally
parallel to the principal axis pass through a convex lens (Fig. 9), the effect
of the two refractions which they undergo, one on entering and the other on
leaving the lens, is to make them all converge approximately to one point F,
which is called the principal focus. The distance A F of the principal focus
from the lens is called the principal focal distance, or more briefly and
usually, the focal length of the lens. The radiant point and its image after
refraction are known as the conjugate foci. In every lens the right line
perpendicular to the two surfaces is the axis of the lens. This is indicated by
the line drawn through the several lenses, as seen in the diagram (Fig. 8).
The point where the axis cuts the surface of the lens is termed the verte.
Parallel rays falling on a double-convex lens are brought to a focus in the
centre of its diameter; conversely, rays diverging from that point are
rendered parallel. Hence the focus of a double-convex lens will be at just
half the distance, or half the length, of the focus of a plano-convex lens
having the same curvature on one side. The distance of the focus from the
lens will depend as much on the degree of curvature as upon the refracting
power (termed the index of refraction) of the glass of which it may be
formed. A lens of crown-glass will have a longer focus than a similar one of
flint-glass; since the latter has a greater refracting power than the former.
For all ordinary practical purposes we may consider the principal focus—as
the focus for parallel rays is termed—of a double-convex lens to be at the
distance of its radius, that is, in its centre of curvature; and that of a plano-
Principal Focus of Convex Lens.—When rays which were originally
parallel to the principal axis pass through a convex lens (Fig. 9), the effect
of the two refractions which they undergo, one on entering and the other on
leaving the lens, is to make them all converge approximately to one point F,
which is called the principal focus. The distance A F of the principal focus
from the lens is called the principal focal distance, or more briefly and
usually, the focal length of the lens. The radiant point and its image after
refraction are known as the conjugate foci. In every lens the right line
perpendicular to the two surfaces is the axis of the lens. This is indicated by
the line drawn through the several lenses, as seen in the diagram (Fig. 8).
The point where the axis cuts the surface of the lens is termed the verte.
Parallel rays falling on a double-convex lens are brought to a focus in the
centre of its diameter; conversely, rays diverging from that point are
rendered parallel. Hence the focus of a double-convex lens will be at just
half the distance, or half the length, of the focus of a plano-convex lens
having the same curvature on one side. The distance of the focus from the
lens will depend as much on the degree of curvature as upon the refracting
power (termed the index of refraction) of the glass of which it may be
formed. A lens of crown-glass will have a longer focus than a similar one of
flint-glass; since the latter has a greater refracting power than the former.
For all ordinary practical purposes we may consider the principal focus—as
the focus for parallel rays is termed—of a double-convex lens to be at the
distance of its radius, that is, in its centre of curvature; and that of a plano-
Page 52
convex lens to be at the distance of twice its radius, that is, at the other end
of the diameter of its sphere of curvature. The converse of all this occurs
when divergent rays are made to fall on a convex lens. Rays already
converging are brought together at a point nearer than the principal focus;
whereas rays diverging from a point within the principal focus are rendered
still more diverging, though in a diminished degree. Rays diverging from
points more distant than the principal focus on either side, are brought to a
focus beyond it: if the point of divergence be within the circle of curvature,
the focus of convergence will be beyond it; and vice-versâ. The same
principles apply equally to a plano-convex lens; allowance being made for
the double distance of its principal focus; and also to a lens whose surfaces
have different curvatures; the principal focus of such a lens is found by
multiplying the radius of one surface by the radius of the other, and dividing
this product by half the sum of the radii.
Fig. 10.—Principal Focus of Concave Lens.
In the case of a concave lens (Fig. 10), rays incident parallel to the principal
axis diverge after passing through; and their directions, if produced
backwards, would approximately meet in a point F; this is its principal
focus. It is, however, only a virtual focus, inasmuch as the emergent rays do
not actually pass through it, whereas the principal focus of a converging
lens is real.
Optical Centre of a Lens.—Secondary Axes.—Let O and O′ (Fig. 11) be
the centres of the two spherical surfaces of a lens. Draw any two parallel
of the diameter of its sphere of curvature. The converse of all this occurs
when divergent rays are made to fall on a convex lens. Rays already
converging are brought together at a point nearer than the principal focus;
whereas rays diverging from a point within the principal focus are rendered
still more diverging, though in a diminished degree. Rays diverging from
points more distant than the principal focus on either side, are brought to a
focus beyond it: if the point of divergence be within the circle of curvature,
the focus of convergence will be beyond it; and vice-versâ. The same
principles apply equally to a plano-convex lens; allowance being made for
the double distance of its principal focus; and also to a lens whose surfaces
have different curvatures; the principal focus of such a lens is found by
multiplying the radius of one surface by the radius of the other, and dividing
this product by half the sum of the radii.
Fig. 10.—Principal Focus of Concave Lens.
In the case of a concave lens (Fig. 10), rays incident parallel to the principal
axis diverge after passing through; and their directions, if produced
backwards, would approximately meet in a point F; this is its principal
focus. It is, however, only a virtual focus, inasmuch as the emergent rays do
not actually pass through it, whereas the principal focus of a converging
lens is real.
Optical Centre of a Lens.—Secondary Axes.—Let O and O′ (Fig. 11) be
the centres of the two spherical surfaces of a lens. Draw any two parallel
Page 53
radii, O I, O′ E, to meet these
surfaces, and let the joining line I E
represent a ray passing through the
lens. This ray makes equal angles
with the normals at I and E, since
these latter are parallel by
construction; hence the incident and
emergent rays S I, E R also make
equal angles with the normals, and
are therefore parallel. In fact, if
tangent planes (indicated by the
dotted lines in the figure) are drawn
at I and E, the whole course of the
Fig. 11.—Principal Centre of Lens. ray S I E R will be the same as if it
had passed through a plate bounded
by these planes.
Let C be the point in which the line I E cuts the principal axis, and let R, R′
denote the radii of the two spherical surfaces. Then from the similarity of
the triangles O C I, O′ C E, we have (O C)/(C O′) = R′/R; which shows that
the point C divides the line of centres O O′ in a definite ratio depending
only on the radii. Every ray whose direction on emergence is parallel to its
direction before entering the lens, must pass through the point C in
traversing the lens; and conversely, every ray which in its course through
the lens traverses the point C, has parallel directions at incidence and
emergence. The point C which possesses this remarkable property is called
the centre, or optical centre, of the lens.
This diagram may also be taken to prove my former proposition, that the
convex lens is practically a form of two prisms combined.
surfaces, and let the joining line I E
represent a ray passing through the
lens. This ray makes equal angles
with the normals at I and E, since
these latter are parallel by
construction; hence the incident and
emergent rays S I, E R also make
equal angles with the normals, and
are therefore parallel. In fact, if
tangent planes (indicated by the
dotted lines in the figure) are drawn
at I and E, the whole course of the
Fig. 11.—Principal Centre of Lens. ray S I E R will be the same as if it
had passed through a plate bounded
by these planes.
Let C be the point in which the line I E cuts the principal axis, and let R, R′
denote the radii of the two spherical surfaces. Then from the similarity of
the triangles O C I, O′ C E, we have (O C)/(C O′) = R′/R; which shows that
the point C divides the line of centres O O′ in a definite ratio depending
only on the radii. Every ray whose direction on emergence is parallel to its
direction before entering the lens, must pass through the point C in
traversing the lens; and conversely, every ray which in its course through
the lens traverses the point C, has parallel directions at incidence and
emergence. The point C which possesses this remarkable property is called
the centre, or optical centre, of the lens.
This diagram may also be taken to prove my former proposition, that the
convex lens is practically a form of two prisms combined.
Page 54
Fig. 12.—Conjugate Foci, one Real, the other Virtual.
Conjugate Foci, one Real, one Virtual.—When two foci are on the same
side of the lens, one (the most distant of the two) must be virtual. For
example, in Fig. 12, if S, S′ are a pair of conjugate foci, one of them S being
between the principal focus F and the lens, rays sent to the lens at a
luminous point at S, will, after emergence, diverge as if from S′; and rays
coming from the other side of the lens, if they converge to S′ before
incidence, will in reality be made to meet in S. As S moves towards the
lens, S′ moves in the same direction more rapidly; and they become
coincident at the surface of the lens.
Formation of Real Images.—Let A B (Fig. 13) be an object in front of a
lens, at a distance less than the principal focal length. It will have a real
image on the other side of the lens. To determine the position of the image
by construction, draw through any point A of the object a line parallel to the
principal axis, meeting the lens in A′. The ray represented by this line will,
after refraction, pass through the principal focus, F, and its intersection with
the secondary axis, A O, determines the position of a, the focus conjugate to
A. We can in like manner determine the position of b, the focus conjugate to
B, another point of the object; and the joining line a b will then be the
magnified image of the line A B. It is evident that if a b were the object, A
B would be the image.
Conjugate Foci, one Real, one Virtual.—When two foci are on the same
side of the lens, one (the most distant of the two) must be virtual. For
example, in Fig. 12, if S, S′ are a pair of conjugate foci, one of them S being
between the principal focus F and the lens, rays sent to the lens at a
luminous point at S, will, after emergence, diverge as if from S′; and rays
coming from the other side of the lens, if they converge to S′ before
incidence, will in reality be made to meet in S. As S moves towards the
lens, S′ moves in the same direction more rapidly; and they become
coincident at the surface of the lens.
Formation of Real Images.—Let A B (Fig. 13) be an object in front of a
lens, at a distance less than the principal focal length. It will have a real
image on the other side of the lens. To determine the position of the image
by construction, draw through any point A of the object a line parallel to the
principal axis, meeting the lens in A′. The ray represented by this line will,
after refraction, pass through the principal focus, F, and its intersection with
the secondary axis, A O, determines the position of a, the focus conjugate to
A. We can in like manner determine the position of b, the focus conjugate to
B, another point of the object; and the joining line a b will then be the
magnified image of the line A B. It is evident that if a b were the object, A
B would be the image.
Page 55
Fig. 13.—Real and Magnified Image.
The figures 12 and 13 represent the cases in which the distance of the object
is respectively greater and less than twice the focal length of the lens.
The focal length of a lens is determined by the convexity of its surfaces and
the refractive power of the material of which it is composed, being
shortened either by an increase of refractive power, or diminution of the
radii of curvature of the faces of the lens. The increase or decrease of
spherical aberration is determined by the shape or curvature of the lens; it is
less in the bi-convex than in other forms. When a lamp or other source of
light is placed at the focus of the rays constituting that portion of its light
which falls upon the lens, the light is so refracted as to become parallel.
Should the source of light be brought nearer to the lens than the focus the
refracted rays are still divergent, though not to the same extent; on the other
hand, if the source be beyond the focus, the refracted rays are rendered
convergent so as to meet at a point which is mathematically related to the
distance of the luminous source from the focus. The former arrangement is
that with which we are most familiar, since it is the ordinary magnifying
glass.
Concave Lenses.
The refracting influence of a concave lens (Fig. 14) will be precisely the
opposite of that of a convex. Rays which fall upon it in a parallel direction
The figures 12 and 13 represent the cases in which the distance of the object
is respectively greater and less than twice the focal length of the lens.
The focal length of a lens is determined by the convexity of its surfaces and
the refractive power of the material of which it is composed, being
shortened either by an increase of refractive power, or diminution of the
radii of curvature of the faces of the lens. The increase or decrease of
spherical aberration is determined by the shape or curvature of the lens; it is
less in the bi-convex than in other forms. When a lamp or other source of
light is placed at the focus of the rays constituting that portion of its light
which falls upon the lens, the light is so refracted as to become parallel.
Should the source of light be brought nearer to the lens than the focus the
refracted rays are still divergent, though not to the same extent; on the other
hand, if the source be beyond the focus, the refracted rays are rendered
convergent so as to meet at a point which is mathematically related to the
distance of the luminous source from the focus. The former arrangement is
that with which we are most familiar, since it is the ordinary magnifying
glass.
Concave Lenses.
The refracting influence of a concave lens (Fig. 14) will be precisely the
opposite of that of a convex. Rays which fall upon it in a parallel direction
Page 56
will be made to diverge as if from the principal focus, which is here called
the negative focus. This will be, for a plano-concave lens, at the distance of
the diameter of the sphere of curvature; and for a double-concave, in the
centre of that sphere.
Fig. 14.—A Virtual Image formed by Concave Lens.
In Fig. 14 A B is the object and a b the image. Rays incident from A and B
parallel to the principal axis will emerge as if they came from the principal
focus F; hence, the points a b are determined by the intersections of the
dotted lines in the figure with the secondary axis, O A, O B. An eye on the
other side of the lens sees the image a b, which is always virtual, erect and
diminished.
In the construction of the microscope, either simple or compound, the
curvature of the lenses employed is usually spherical. Convergent lenses,
with spherical curvatures, have the defect of not bringing all the rays of
light which pass through them to one and the same focus. Each circle of
rays from the axis of the lens to its circumference has a different focus, as
shown in Fig. 15. The rays a a, which pass through the lens near its
circumference, are seen to be more refracted, or come to a focus at a shorter
distance behind it than the rays b b, which pass through near its centre or
axis, and are less refracted. The consequence of this defect of lenses with
spherical curvatures, which is called spherical aberration, is that a well-
defined image or picture is not formed by them, for when the object is
focussed, for the circumferential rays, the picture projected to the eye is
the negative focus. This will be, for a plano-concave lens, at the distance of
the diameter of the sphere of curvature; and for a double-concave, in the
centre of that sphere.
Fig. 14.—A Virtual Image formed by Concave Lens.
In Fig. 14 A B is the object and a b the image. Rays incident from A and B
parallel to the principal axis will emerge as if they came from the principal
focus F; hence, the points a b are determined by the intersections of the
dotted lines in the figure with the secondary axis, O A, O B. An eye on the
other side of the lens sees the image a b, which is always virtual, erect and
diminished.
In the construction of the microscope, either simple or compound, the
curvature of the lenses employed is usually spherical. Convergent lenses,
with spherical curvatures, have the defect of not bringing all the rays of
light which pass through them to one and the same focus. Each circle of
rays from the axis of the lens to its circumference has a different focus, as
shown in Fig. 15. The rays a a, which pass through the lens near its
circumference, are seen to be more refracted, or come to a focus at a shorter
distance behind it than the rays b b, which pass through near its centre or
axis, and are less refracted. The consequence of this defect of lenses with
spherical curvatures, which is called spherical aberration, is that a well-
defined image or picture is not formed by them, for when the object is
focussed, for the circumferential rays, the picture projected to the eye is
Page 57
rendered indistinct by a halo or confusion produced by the central rays
falling in a circle of dissipation, before they have come to a focus. On the
other hand, when placed in the focus of the central rays, the picture formed
by them is rendered indistinct by the halo produced by the circumferential
rays, which have already come to a focus and crossed, and now fall in a
state of divergence, forming a circle of dissipation. The grosser defects of
spherical aberration are corrected by cutting off the passage of the rays a a,
through the circumferences of the lens, by means of a stop diaphragm, so
that the central rays, b b, only are concerned in the formation of the image.
This defect is reduced to a minimum, by using the meniscus form of lens,
which is the segment of an ellipsoid instead of a sphere.
Fig. 15.—Spherical Aberration of Lens.
The ellipse and the hyperbola are forms of lenses in which the curvature
diminishes from the central ray, or axis, to the circumference b; and
mathematicians have shown that spherical aberration may be practically got
rid of by employing lenses whose sections are ellipses or hyperbolas. The
remarkable discovery of these forms of lenses is attributed to Descartes,
who mathematically demonstrated the fact.
If a l, a l′, for example (Fig. 16) be part of an ellipse whose greater axis is to
the distance between its foci f f as the index of refraction is to unity, then
parallel rays r l′, r′′ l incident upon the elliptical surface l′ a l, will be
falling in a circle of dissipation, before they have come to a focus. On the
other hand, when placed in the focus of the central rays, the picture formed
by them is rendered indistinct by the halo produced by the circumferential
rays, which have already come to a focus and crossed, and now fall in a
state of divergence, forming a circle of dissipation. The grosser defects of
spherical aberration are corrected by cutting off the passage of the rays a a,
through the circumferences of the lens, by means of a stop diaphragm, so
that the central rays, b b, only are concerned in the formation of the image.
This defect is reduced to a minimum, by using the meniscus form of lens,
which is the segment of an ellipsoid instead of a sphere.
Fig. 15.—Spherical Aberration of Lens.
The ellipse and the hyperbola are forms of lenses in which the curvature
diminishes from the central ray, or axis, to the circumference b; and
mathematicians have shown that spherical aberration may be practically got
rid of by employing lenses whose sections are ellipses or hyperbolas. The
remarkable discovery of these forms of lenses is attributed to Descartes,
who mathematically demonstrated the fact.
If a l, a l′, for example (Fig. 16) be part of an ellipse whose greater axis is to
the distance between its foci f f as the index of refraction is to unity, then
parallel rays r l′, r′′ l incident upon the elliptical surface l′ a l, will be
Page 58
refracted by the single action of that surface into lines which would meet
exactly in the farther focus f, if there were no second surface intervening
between l a l′ and f. But as every useful lens must have two surfaces, we
have only to describe a circle l a′ l′ round f as a centre, for the second
surface of the lens l′ l.
Fig. 16.—Converging Meniscus.
As all the rays refracted at the surface l a l′ converge accurately to f, and as
the circular surface l a′ l′ is perpendicular to every one of the refracted rays,
all these rays will go on to f without suffering any refraction at the circular
surface. Hence it should follow, that a meniscus whose convex surface is
part of an ellipsoid, and whose concave surface is part of any spherical
surface whose centre is in the farther focus, will have no appreciable
spherical aberration, and will refract parallel rays incident on its convex
surface to the farther focus.
The spherical form of lens is that most generally used in the construction of
the microscope. If a true elliptical or hyperbolic curve could be ground,
lenses would very nearly approach perfection, and spherical aberration
would be considerably reduced. Even this defect can be further reduced in
exactly in the farther focus f, if there were no second surface intervening
between l a l′ and f. But as every useful lens must have two surfaces, we
have only to describe a circle l a′ l′ round f as a centre, for the second
surface of the lens l′ l.
Fig. 16.—Converging Meniscus.
As all the rays refracted at the surface l a l′ converge accurately to f, and as
the circular surface l a′ l′ is perpendicular to every one of the refracted rays,
all these rays will go on to f without suffering any refraction at the circular
surface. Hence it should follow, that a meniscus whose convex surface is
part of an ellipsoid, and whose concave surface is part of any spherical
surface whose centre is in the farther focus, will have no appreciable
spherical aberration, and will refract parallel rays incident on its convex
surface to the farther focus.
The spherical form of lens is that most generally used in the construction of
the microscope. If a true elliptical or hyperbolic curve could be ground,
lenses would very nearly approach perfection, and spherical aberration
would be considerably reduced. Even this defect can be further reduced in
Page 59
practice by observing a certain ratio between the
radii of the anterior and posterior surfaces of lenses;
thus the spherical aberration of a lens, the radius of
one surface of which is six or seven times greater
than that of the other, will be much reduced when its
more convex surface is turned forward to receive
parallel rays, than when its less convex surface is
turned forwards. It should be borne in mind that in
lenses having curvatures of the kind the object
would only be correctly seen in focus at one point—
the mathematical or geometrical axis of the lens. Fig. 17.—Aplanatic Doublet.
Chromatic Aberration.—We have yet to deal with one of the most
important of the phenomena of light, CHROMATIC ABERRATION, upon the
correction of which, in convex lenses in particular, the perfection of the
objective of the microscope so much depends. Chromatism arises from the
unequal refrangibility and length of the different coloured rays of light that
together go to make up white light; but which, when treated of in optics, is
always associated with achromatism, so that a combination of prisms, or
lenses, is said to be achromatic when the coloured rays arising from the
dispersion of the pencil of light refracted through them are combined in due
proportions as they are in perfectly white light.
A lens, however, of uniform material will not form a single white image,
but a series of images of all colours of the spectrum, arranged at different
distances, the violet being nearest, and the red the most remote, every other
colour giving a blurred image; the superposition of these and the blending
of the different elementary rays furnishing a complete explanation of the
beautiful phenomenon of the rainbow. Sharpness of outline is rendered
quite impossible in such a case, and this source of confusion is known as
chromatic aberration.
In order to ascertain whether it is possible to remedy this evil by combining
lenses of two different materials, Newton made some trials with a
compound prism composed of glass and water (the latter containing a little
sugar of lead), and he found it impossible by any arrangement of these two,
or by other substances, to produce deviation of the transmitted light without
radii of the anterior and posterior surfaces of lenses;
thus the spherical aberration of a lens, the radius of
one surface of which is six or seven times greater
than that of the other, will be much reduced when its
more convex surface is turned forward to receive
parallel rays, than when its less convex surface is
turned forwards. It should be borne in mind that in
lenses having curvatures of the kind the object
would only be correctly seen in focus at one point—
the mathematical or geometrical axis of the lens. Fig. 17.—Aplanatic Doublet.
Chromatic Aberration.—We have yet to deal with one of the most
important of the phenomena of light, CHROMATIC ABERRATION, upon the
correction of which, in convex lenses in particular, the perfection of the
objective of the microscope so much depends. Chromatism arises from the
unequal refrangibility and length of the different coloured rays of light that
together go to make up white light; but which, when treated of in optics, is
always associated with achromatism, so that a combination of prisms, or
lenses, is said to be achromatic when the coloured rays arising from the
dispersion of the pencil of light refracted through them are combined in due
proportions as they are in perfectly white light.
A lens, however, of uniform material will not form a single white image,
but a series of images of all colours of the spectrum, arranged at different
distances, the violet being nearest, and the red the most remote, every other
colour giving a blurred image; the superposition of these and the blending
of the different elementary rays furnishing a complete explanation of the
beautiful phenomenon of the rainbow. Sharpness of outline is rendered
quite impossible in such a case, and this source of confusion is known as
chromatic aberration.
In order to ascertain whether it is possible to remedy this evil by combining
lenses of two different materials, Newton made some trials with a
compound prism composed of glass and water (the latter containing a little
sugar of lead), and he found it impossible by any arrangement of these two,
or by other substances, to produce deviation of the transmitted light without
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separation into its component colours. If this ratio were the same for all
substances, as Newton supposed, achromatism would be impossible; but, in
fact, its value varies greatly, and is far greater for flint than for crown glass.
If two prisms of these substances, of small refracting angles, be combined
into one, with their edges turned in opposite directions, they will
achromatise each other.
The chromatism of lenses may, however, be somewhat further reduced by
stopping out the marginal rays, but as the most perfect correction possible is
required when lenses are combined for microscopic uses, other means of
correction are resorted to, as will be seen hereafter. I shall first proceed to
show the deviations which rays of white light undergo in traversing a lens.
If parallel rays of light pass through a double-convex lens the violet rays,
the most refrangible of them, will come to a focus at a point much nearer to
the lens than the focus of the red rays, which are the least refrangible; and
the intermediate rays of the spectrum will be focussed at points between the
red and the violet. A screen held at either of these foci will show an image
with prismatic fringes. The white light, A A′′ (Fig. 18), falling on the
marginal portion of the lens is so far decomposed that the violet rays are
brought to a focus at C, and crossing there, diverge again and pass on to F
F′, while the red rays, B B′′, do not come to a focus until they reach the
point D, and cross the divergent violet rays, E E′. The foci of the
intermediary rays of the spectrum (red, green, and blue) are intermediate
between these extremes. The distance, C D, limiting the blue or violet, and
the red is termed the longitudinal chromatic aberration of the lens. If the
image be received upon a screen placed at C, violet will predominate and
appear surrounded by a prismatic fringe, in which violet will predominate.
If the screen be now shifted to D, the image will have a predominant red
tint, surrounded by a series of coloured fringes in an inverted order to those
seen in the former experiment. The line E E′ joins the points of intersection
between the violet and red rays, and this marks the mean focus, the point
where the coloured rays will be least apparent.
substances, as Newton supposed, achromatism would be impossible; but, in
fact, its value varies greatly, and is far greater for flint than for crown glass.
If two prisms of these substances, of small refracting angles, be combined
into one, with their edges turned in opposite directions, they will
achromatise each other.
The chromatism of lenses may, however, be somewhat further reduced by
stopping out the marginal rays, but as the most perfect correction possible is
required when lenses are combined for microscopic uses, other means of
correction are resorted to, as will be seen hereafter. I shall first proceed to
show the deviations which rays of white light undergo in traversing a lens.
If parallel rays of light pass through a double-convex lens the violet rays,
the most refrangible of them, will come to a focus at a point much nearer to
the lens than the focus of the red rays, which are the least refrangible; and
the intermediate rays of the spectrum will be focussed at points between the
red and the violet. A screen held at either of these foci will show an image
with prismatic fringes. The white light, A A′′ (Fig. 18), falling on the
marginal portion of the lens is so far decomposed that the violet rays are
brought to a focus at C, and crossing there, diverge again and pass on to F
F′, while the red rays, B B′′, do not come to a focus until they reach the
point D, and cross the divergent violet rays, E E′. The foci of the
intermediary rays of the spectrum (red, green, and blue) are intermediate
between these extremes. The distance, C D, limiting the blue or violet, and
the red is termed the longitudinal chromatic aberration of the lens. If the
image be received upon a screen placed at C, violet will predominate and
appear surrounded by a prismatic fringe, in which violet will predominate.
If the screen be now shifted to D, the image will have a predominant red
tint, surrounded by a series of coloured fringes in an inverted order to those
seen in the former experiment. The line E E′ joins the points of intersection
between the violet and red rays, and this marks the mean focus, the point
where the coloured rays will be least apparent.
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Fig. 18.—Chromatic Aberration of Lens.
In the early part of this century the optical correction of chromatic
aberration was partially brought about by combining a convex lens of
crown-glass with a concave lens of flint-glass, in the proportion of which
these two kinds of glass respectively refract and disperse rays of light; so
that the one medium may by equal and contrary dispersion neutralise the
dispersion caused by the other, without at the same time wholly neutralising
its refraction. It is a curious fact that the media found most available for the
purpose should be a combination of crown and flint-glass, of crown-glass
whose index of refraction is 1·519, and dispersive power 0·036, and of
flint-glass whose index of refraction is 1·589, and dispersive power 0·0393.
The focal length of the convex crown-glass lens must be 41⁄3 inches, and
that of the concave flint-glass lens 72⁄3 inches, and the combined focal
length 10 inches. The diagram (Fig. 19) shows how rays of light are brought
to a focus, nearly free from colour. The small amount of residual colour in
such a combination is termed the secondary spectrum; the violet ray F Y,
crossing the axis of the lens at V, and going to the upper end P of the
spectrum, the red ray F B going to the lower end T. But as the flint-glass
lens l l, on the prism A a C, which receives the rays F V, F R, at the same
points, is interposed, these rays will unite at f, and form a small circle of
white light, the ray S F being now refracted without colour from its
primitive direction S F Y into the direction F f. In like manner, the
corresponding ray S F′ will be refracted to f, and a white colourless image
be the result.
In the early part of this century the optical correction of chromatic
aberration was partially brought about by combining a convex lens of
crown-glass with a concave lens of flint-glass, in the proportion of which
these two kinds of glass respectively refract and disperse rays of light; so
that the one medium may by equal and contrary dispersion neutralise the
dispersion caused by the other, without at the same time wholly neutralising
its refraction. It is a curious fact that the media found most available for the
purpose should be a combination of crown and flint-glass, of crown-glass
whose index of refraction is 1·519, and dispersive power 0·036, and of
flint-glass whose index of refraction is 1·589, and dispersive power 0·0393.
The focal length of the convex crown-glass lens must be 41⁄3 inches, and
that of the concave flint-glass lens 72⁄3 inches, and the combined focal
length 10 inches. The diagram (Fig. 19) shows how rays of light are brought
to a focus, nearly free from colour. The small amount of residual colour in
such a combination is termed the secondary spectrum; the violet ray F Y,
crossing the axis of the lens at V, and going to the upper end P of the
spectrum, the red ray F B going to the lower end T. But as the flint-glass
lens l l, on the prism A a C, which receives the rays F V, F R, at the same
points, is interposed, these rays will unite at f, and form a small circle of
white light, the ray S F being now refracted without colour from its
primitive direction S F Y into the direction F f. In like manner, the
corresponding ray S F′ will be refracted to f, and a white colourless image
be the result.
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Fig. 19.—Correction of Chromatic Aberration.
The achromatic aplanatic objective constructed on the optical formula
enunciated, did not meet all the difficulties experienced by the skilled
microscopist, in obtaining resolution of the finest test objects, and whereby
the intrinsic value of the objective (in his estimation) must stand or fall.
There were other disturbing residuary elements besides those of the
secondary spectrum, and which at a later period were met by the practical
skill of the optician, who applied the screw-collar, and by means of which
the back lens of the objective is made to approach the front lens, thus more
accurately shortening the distance between the eye-piece, where the image
is eventually formed, and the back lens of the objective.
In this diagram L L is a convex lens of crown-glass, and l l a concave one of
flint-glass. A convex lens will refract a ray of light (S) falling at F on it
exactly in the same manner as the prism A B C, whose faces touch the two
surfaces of the lens at the points where the ray enters, and quits. The ray S
F, thus refracted by the lens L L, or prism A B C, would have formed a
spectrum (P T) on a screen or wall, had there been no other lens.
The achromatic aplanatic objective constructed on the optical formula
enunciated, did not meet all the difficulties experienced by the skilled
microscopist, in obtaining resolution of the finest test objects, and whereby
the intrinsic value of the objective (in his estimation) must stand or fall.
There were other disturbing residuary elements besides those of the
secondary spectrum, and which at a later period were met by the practical
skill of the optician, who applied the screw-collar, and by means of which
the back lens of the objective is made to approach the front lens, thus more
accurately shortening the distance between the eye-piece, where the image
is eventually formed, and the back lens of the objective.
In this diagram L L is a convex lens of crown-glass, and l l a concave one of
flint-glass. A convex lens will refract a ray of light (S) falling at F on it
exactly in the same manner as the prism A B C, whose faces touch the two
surfaces of the lens at the points where the ray enters, and quits. The ray S
F, thus refracted by the lens L L, or prism A B C, would have formed a
spectrum (P T) on a screen or wall, had there been no other lens.
Page 63
Fig. 20.—Virtual Image formed by Convex Lens.
Formation of Virtual Images.—The normal eye possesses a considerable
power of adjusting itself to form a distinct image of objects placed at
varying distances; the nearer, within a certain limit, the larger it appears,
and the more distinctly the details are brought out. When brought within a
distance of two or three inches, the images become blurred or quite
indistinct, and when brought closer to the eye, cannot be seen at all, and it
simply obstructs the light. Now the utility of a convex lens, when
interposed between the object and the eye, consists in reducing the
divergence of the rays forming the several pencils which issue from it, and
send images to the retina in a state of moderate divergence, that is, as if they
had issued from an object beyond the nearest point of distinct vision, and so
that a more clearly defined image may reach the sensitive membrane of the
eye. But, not only is the course of the several rays in each pencil altered as
regards the rest, but the course of the pencils themselves is changed, so that
they enter the eye under an angle corresponding with that under which they
would have arrived from a larger object situated at a greater distance, and
thus the picture formed by any object corresponds in all respects with one
which would have been made by the same object increased in its
dimensions and viewed at the smallest ordinary distance of distinct vision.
For instance, let an object A B (Fig. 20) be placed between a convex lens
and its principal focus. Then the foci conjugate to the points A B are virtual,
and their positions can be found by construction from the consideration that
rays through A, B, parallel to the principal axis, will be refracted to F, the
Formation of Virtual Images.—The normal eye possesses a considerable
power of adjusting itself to form a distinct image of objects placed at
varying distances; the nearer, within a certain limit, the larger it appears,
and the more distinctly the details are brought out. When brought within a
distance of two or three inches, the images become blurred or quite
indistinct, and when brought closer to the eye, cannot be seen at all, and it
simply obstructs the light. Now the utility of a convex lens, when
interposed between the object and the eye, consists in reducing the
divergence of the rays forming the several pencils which issue from it, and
send images to the retina in a state of moderate divergence, that is, as if they
had issued from an object beyond the nearest point of distinct vision, and so
that a more clearly defined image may reach the sensitive membrane of the
eye. But, not only is the course of the several rays in each pencil altered as
regards the rest, but the course of the pencils themselves is changed, so that
they enter the eye under an angle corresponding with that under which they
would have arrived from a larger object situated at a greater distance, and
thus the picture formed by any object corresponds in all respects with one
which would have been made by the same object increased in its
dimensions and viewed at the smallest ordinary distance of distinct vision.
For instance, let an object A B (Fig. 20) be placed between a convex lens
and its principal focus. Then the foci conjugate to the points A B are virtual,
and their positions can be found by construction from the consideration that
rays through A, B, parallel to the principal axis, will be refracted to F, the
Page 64
principal focus on the other side. The refracted rays, if produced backwards,
must meet the secondary axis O A, O B in the required points. An eye
placed on the other side of the lens will accordingly see a virtual image
erect, magnified, and at a greater distance from the lens than the object.
This is the principle of the simple microscope.
The Human Eye.
To gain a clear insight into the mode in which a single lens serves to
magnify objects, it will be necessary to revert to the phenomena of ordinary
vision. An eye free from any defect has a considerable power of adjusting
itself to very considerable distances. One of the special functions of the eye
is bringing the rays of light, by a series of dioptric mechanisms, to a perfect
focus on its nervous sensitive layer, the retina. The eye in this respect has
been compared to a photographic camera. But this is not quite correct. The
retina is destined simply to receive the images furnished by the dioptric
apparatus, and has no influence upon the formation of these images. The
luminous rays are refracted by the dioptric apparatus; the images would be
formed quite as well—indeed, even better in certain cases—if the retina
were not there. The dioptric apparatus and its action are absolutely
independent of the retina.
The same laws with regard to the passage of the rays of light into the human
eye hold good, as those already enunciated in the previous pages. As to
change of direction when rays are passing obliquely from a medium of low
density to that of a higher density, i.e., it changes its course, and is bent
towards the perpendicular. On leaving the denser for the rarer medium it is
bent once more from the perpendicular. Again, by means of a convex lens,
the rays of light from one source will be refracted so as to meet at a point
termed the principal focus of vision.
In the eye there are several surfaces separating the different media where
refraction takes place. The refractive index of the aqueous humour and the
tears poured out by the lachrymal gland is almost equal to that of the
cornea. We may, therefore, speak of the refracting surfaces as three, viz.:
Anterior surface of cornea, anterior surface of lens, and posterior surface of
must meet the secondary axis O A, O B in the required points. An eye
placed on the other side of the lens will accordingly see a virtual image
erect, magnified, and at a greater distance from the lens than the object.
This is the principle of the simple microscope.
The Human Eye.
To gain a clear insight into the mode in which a single lens serves to
magnify objects, it will be necessary to revert to the phenomena of ordinary
vision. An eye free from any defect has a considerable power of adjusting
itself to very considerable distances. One of the special functions of the eye
is bringing the rays of light, by a series of dioptric mechanisms, to a perfect
focus on its nervous sensitive layer, the retina. The eye in this respect has
been compared to a photographic camera. But this is not quite correct. The
retina is destined simply to receive the images furnished by the dioptric
apparatus, and has no influence upon the formation of these images. The
luminous rays are refracted by the dioptric apparatus; the images would be
formed quite as well—indeed, even better in certain cases—if the retina
were not there. The dioptric apparatus and its action are absolutely
independent of the retina.
The same laws with regard to the passage of the rays of light into the human
eye hold good, as those already enunciated in the previous pages. As to
change of direction when rays are passing obliquely from a medium of low
density to that of a higher density, i.e., it changes its course, and is bent
towards the perpendicular. On leaving the denser for the rarer medium it is
bent once more from the perpendicular. Again, by means of a convex lens,
the rays of light from one source will be refracted so as to meet at a point
termed the principal focus of vision.
In the eye there are several surfaces separating the different media where
refraction takes place. The refractive index of the aqueous humour and the
tears poured out by the lachrymal gland is almost equal to that of the
cornea. We may, therefore, speak of the refracting surfaces as three, viz.:
Anterior surface of cornea, anterior surface of lens, and posterior surface of
Page 65
lens; and also of the refracting media as three—the aqueous humour, the
lens, and vitreous humour. These several bodies are so adapted in the
normal eye that parallel rays falling on the cornea are converged to a focus
at the most sensitive spot (the yellow spot, or fovea centralis) in the retina, a
point representing to the principal focus of the eye. A line drawn from this
point through the centre of the cornea is called the optic axis of the eye-ball.
Fig. 21.—Nerve and Stellate Cell Layer of Cornea,6 stained by chloride of gold;
magnified 300 diameters. a, Nerve cells. b, Stellate cells.
lens, and vitreous humour. These several bodies are so adapted in the
normal eye that parallel rays falling on the cornea are converged to a focus
at the most sensitive spot (the yellow spot, or fovea centralis) in the retina, a
point representing to the principal focus of the eye. A line drawn from this
point through the centre of the cornea is called the optic axis of the eye-ball.
Fig. 21.—Nerve and Stellate Cell Layer of Cornea,6 stained by chloride of gold;
magnified 300 diameters. a, Nerve cells. b, Stellate cells.
Page 66
Fig. 22.—Anterior section of Eye, showing changed form of lens during the act of
accommodation, a voluntary action in the eye. M, Ciliary muscle; I, Iris; L, Lens;
V, Vitreous Humour; A, Aqueous Humour; C, Cornea and optic axis.
But as we are able to form a distinct image of near objects, and as we notice
when we turn our gaze from far to near objects there is a distinct feeling of
muscular effort in the eyes, there must be some means whereby the eye can
readily adapt itself for focussing near and distant objects. In a photographic
camera the focus can be readily altered, either by changing the lenses,
employing a lens of greater or less curvature, or by altering the distance of
the screen from the lens. The last method is obviously impossible in the
rigid eye-ball, and therefore the act of focussing for near and distant objects
is associated with a change in the curvature of the lens, a faculty of the eye
termed accommodation (Fig. 22), a change chiefly accomplished by the
ciliary (muscle) processes, which pull the lens forwards and inwards by
virtual contracting power of the ciliary muscle, and by which its suspensory
ligament is relaxed, and the front of the lens allowed to bulge forward. In
every case, however, accommodation is associated with contraction of the
iris, the special function of which is that of a limiting diaphragm (an iris-
diaphragm), Fig. 23.
In an ordinary spherical bi-convex lens, as already pointed out, the rays of
light passing through the periphery of the lens come to a focus at a nearer
point than the rays passing through the central portion. In this way a certain
amount of blurring of the image takes place, and which, in optical language,
is termed spherical aberration. This defect of the eye is capable of
accommodation, a voluntary action in the eye. M, Ciliary muscle; I, Iris; L, Lens;
V, Vitreous Humour; A, Aqueous Humour; C, Cornea and optic axis.
But as we are able to form a distinct image of near objects, and as we notice
when we turn our gaze from far to near objects there is a distinct feeling of
muscular effort in the eyes, there must be some means whereby the eye can
readily adapt itself for focussing near and distant objects. In a photographic
camera the focus can be readily altered, either by changing the lenses,
employing a lens of greater or less curvature, or by altering the distance of
the screen from the lens. The last method is obviously impossible in the
rigid eye-ball, and therefore the act of focussing for near and distant objects
is associated with a change in the curvature of the lens, a faculty of the eye
termed accommodation (Fig. 22), a change chiefly accomplished by the
ciliary (muscle) processes, which pull the lens forwards and inwards by
virtual contracting power of the ciliary muscle, and by which its suspensory
ligament is relaxed, and the front of the lens allowed to bulge forward. In
every case, however, accommodation is associated with contraction of the
iris, the special function of which is that of a limiting diaphragm (an iris-
diaphragm), Fig. 23.
In an ordinary spherical bi-convex lens, as already pointed out, the rays of
light passing through the periphery of the lens come to a focus at a nearer
point than the rays passing through the central portion. In this way a certain
amount of blurring of the image takes place, and which, in optical language,
is termed spherical aberration. This defect of the eye is capable of
Page 67
correction in three possible ways, and which it may be well to repeat: 1. By
making the refractive index of the lens higher at its centre than at its
circumference; (2) By making the curvature of the lens less near the
circumference than at the centre; (3) By stopping out the peripheral rays of
light by a diaphragm. The two latter methods are those resorted to in most
optical instruments.
Fig. 23.—1. Equatorial section of Eyeball, showing Iris and Ciliary Processes,
after washing away the pigment, × three diameters.
2. Nerves of the Cornea of Kitten’s Eye, stained with iodine.
3. Fibres or Tubules of Lens, × 250, seen to be made up of superimposed crenated
layers, and is therefore not homogeneous in structure, but made up of a number of
extremely fine tubules, whose curvatures are nearly spherical.
In the human eye an attempt is made to apply all these methods, but the
most important is the third, that of applying the diaphragm formed by the
iris, a circular semi-muscular curtain lying just in front of the anterior
surface of the lens. The iris is also furnished with a layer of pigmental cells
which effectually stop out all peripheral rays of light that otherwise would
pass into the eye, creating circles of diffusion of a disturbing nature to
perfect vision. This delicate membrane, then, is kept in constant action by a
two-fold nerve supply, derived from five or six sources, which it is
unnecessary to describe at length. But the eye, with all its marvellous
adaptations, has an obvious defect, that of secondary or uncorrected
chromatic aberration.
making the refractive index of the lens higher at its centre than at its
circumference; (2) By making the curvature of the lens less near the
circumference than at the centre; (3) By stopping out the peripheral rays of
light by a diaphragm. The two latter methods are those resorted to in most
optical instruments.
Fig. 23.—1. Equatorial section of Eyeball, showing Iris and Ciliary Processes,
after washing away the pigment, × three diameters.
2. Nerves of the Cornea of Kitten’s Eye, stained with iodine.
3. Fibres or Tubules of Lens, × 250, seen to be made up of superimposed crenated
layers, and is therefore not homogeneous in structure, but made up of a number of
extremely fine tubules, whose curvatures are nearly spherical.
In the human eye an attempt is made to apply all these methods, but the
most important is the third, that of applying the diaphragm formed by the
iris, a circular semi-muscular curtain lying just in front of the anterior
surface of the lens. The iris is also furnished with a layer of pigmental cells
which effectually stop out all peripheral rays of light that otherwise would
pass into the eye, creating circles of diffusion of a disturbing nature to
perfect vision. This delicate membrane, then, is kept in constant action by a
two-fold nerve supply, derived from five or six sources, which it is
unnecessary to describe at length. But the eye, with all its marvellous
adaptations, has an obvious defect, that of secondary or uncorrected
chromatic aberration.
Page 68
Chromatic Aberration of the Eye.—White light, as previously explained,
is composed of different wave lengths; and accordingly as these undulations
are either longer or shorter, so do they produce on the eye the impression of
different colours. We have seen how a pencil of white light may, by means
of a prism, be decomposed into a multi-coloured band. In an ordinary
magnifying reading-glass these coloured fringes are always seen around the
margins. In practical optics chromatic aberration is partially corrected by
employing two different kinds of glass in the construction of certain
combined lenses. In the human eye chromatism cannot be corrected in this
way; hence a blue light and a red light placed at the same distance from the
eye appears to be unequally distant: the red light requiring greater
accommodation in the eye than the blue, and this accordingly appears to be
the nearer of the two.
This visual error may be experimentally shown and explained. There is a
kind of glass which at first sight appears dark blue or violet, but which
really contains a great deal of red. Take an ordinary microscope lamp,
having a metal or opaque chimney, and drill a circular hole in it, about 3
mm. in diameter. This opening should be just at the height of the flame;
cover it over with a piece of ground glass and a piece of the red-blue glass.
Thus will be formed a luminous point whose light is composed of red and
blue, i.e., of colours far apart from each other in the spectrum.
is composed of different wave lengths; and accordingly as these undulations
are either longer or shorter, so do they produce on the eye the impression of
different colours. We have seen how a pencil of white light may, by means
of a prism, be decomposed into a multi-coloured band. In an ordinary
magnifying reading-glass these coloured fringes are always seen around the
margins. In practical optics chromatic aberration is partially corrected by
employing two different kinds of glass in the construction of certain
combined lenses. In the human eye chromatism cannot be corrected in this
way; hence a blue light and a red light placed at the same distance from the
eye appears to be unequally distant: the red light requiring greater
accommodation in the eye than the blue, and this accordingly appears to be
the nearer of the two.
This visual error may be experimentally shown and explained. There is a
kind of glass which at first sight appears dark blue or violet, but which
really contains a great deal of red. Take an ordinary microscope lamp,
having a metal or opaque chimney, and drill a circular hole in it, about 3
mm. in diameter. This opening should be just at the height of the flame;
cover it over with a piece of ground glass and a piece of the red-blue glass.
Thus will be formed a luminous point whose light is composed of red and
blue, i.e., of colours far apart from each other in the spectrum.
Page 69
Fig. 24.—Chromatic Aberration of Eye, showing the wave differences of the blue
and red rays of light (Landolt).
If rays coming from this point enter the eye, the blue rays (Fig. 24), being
more strongly reflected than the red, will come to a focus sooner than the
latter. The red rays, on the contrary, will be brought to a focus later than the
blue, while the latter, past their focus, are diverging. Let A B C D (Fig. 24)
be the section of a pencil of rays given off from a red-blue point sufficiently
distant so that these rays may be regarded as parallel. The focus of the blue
is at b, that of the red at r.
An eye is adapted to the distance of the luminous point when the circle of
diffusion, received upon the retina, is at its minimum. This is the case when
the sentient layer of the retina lies between the two foci E. In this case the
point will appear as a small circle, composed of the two colours, that is to
say—violet. If the retina be in front of this point, at the focus of the blue
rays for instance, the eye will perceive a blue point surrounded by a red
circle, the latter being formed by the periphery of the luminous cone of red
rays, which are focussed only after having passed the retina. The blue point
will become a circle of diffusion larger in proportion as the retina is nearer
the dioptric system, or as the focus for blue is farther behind it. But the blue
circle will always be surrounded by a red ring. If, on the contrary, the retina
is behind the focus for red, the blue cone will be greater in diameter than the
red, and we shall have a red circle of diffusion, larger in proportion as the
retina is farther from the focus, but always surrounded by a blue ring M. If
the blue-red point is five metres, or more, distant, the emmetropic7 eye will
evidently see it more distinctly, i.e., as a small violet point; the hyperopic
eye, whose retina is situated in front of the focus of its dioptric system, will
see a blue circle, surrounded by red; the myopic eye, whose retina is behind
its focus, will see a red circle, surrounded by blue. The size of these circles
will be either larger or smaller when the principal focus of the eye is either
in front of or behind the retina.8
The refractive surfaces of a perfectly formed eye are very like an ellipsoid
of revolution with two axes, one of which, the major axis of the ellipse, is at
the same time the optic axis and that of rotation; the other is perpendicular
to it, and is equal in all meridians. Eyes, however, perfectly constructed are
and red rays of light (Landolt).
If rays coming from this point enter the eye, the blue rays (Fig. 24), being
more strongly reflected than the red, will come to a focus sooner than the
latter. The red rays, on the contrary, will be brought to a focus later than the
blue, while the latter, past their focus, are diverging. Let A B C D (Fig. 24)
be the section of a pencil of rays given off from a red-blue point sufficiently
distant so that these rays may be regarded as parallel. The focus of the blue
is at b, that of the red at r.
An eye is adapted to the distance of the luminous point when the circle of
diffusion, received upon the retina, is at its minimum. This is the case when
the sentient layer of the retina lies between the two foci E. In this case the
point will appear as a small circle, composed of the two colours, that is to
say—violet. If the retina be in front of this point, at the focus of the blue
rays for instance, the eye will perceive a blue point surrounded by a red
circle, the latter being formed by the periphery of the luminous cone of red
rays, which are focussed only after having passed the retina. The blue point
will become a circle of diffusion larger in proportion as the retina is nearer
the dioptric system, or as the focus for blue is farther behind it. But the blue
circle will always be surrounded by a red ring. If, on the contrary, the retina
is behind the focus for red, the blue cone will be greater in diameter than the
red, and we shall have a red circle of diffusion, larger in proportion as the
retina is farther from the focus, but always surrounded by a blue ring M. If
the blue-red point is five metres, or more, distant, the emmetropic7 eye will
evidently see it more distinctly, i.e., as a small violet point; the hyperopic
eye, whose retina is situated in front of the focus of its dioptric system, will
see a blue circle, surrounded by red; the myopic eye, whose retina is behind
its focus, will see a red circle, surrounded by blue. The size of these circles
will be either larger or smaller when the principal focus of the eye is either
in front of or behind the retina.8
The refractive surfaces of a perfectly formed eye are very like an ellipsoid
of revolution with two axes, one of which, the major axis of the ellipse, is at
the same time the optic axis and that of rotation; the other is perpendicular
to it, and is equal in all meridians. Eyes, however, perfectly constructed are
Page 70
rarely met with. The curvature of the cornea is nearly always greater in one
meridian than in another. Its surfaces then cannot be regarded as entirely
belonging to an ellipsoid of revolution, since the solid figure, of which the
former would constitute a part, has not only two axes, but three, and these
unequal. This irregularity is not, however, always great enough to produce
discomfort and it is therefore disregarded. But in other cases the difference
of curvature in the different meridians of the eye attain to a higher degree,
and vision falls far below the average.
The refractive anomaly alluded to is
termed astigmatism (from the Greek,
α privative, στιγμα, a point—
inability to see a point). The way in
which objects appear to such a
person will mainly result from the
way in which he sees a point. Take,
for example, the vertical to be the
most, and the horizontal to be the
least, refractive meridian: place a
vertical line (Fig. 25, I) at a stated
distance before the eye, and the line
will appear elongated, owing to the
diffusion image of each of the points
Fig. 25.—Lines as seen by the Astigmatic. composing it. It will also seem to be
somewhat broadened, as at II. If the
vertical meridian is adapted to the distance of the vertical, the line will
appear very diffuse and broadened, as at III. All these little diffusion lines
overlap each other, and give the line an elongated appearance. Hence a
straight line is seen distinctly by an astigmatic eye only when the meridian
to which it is perpendicular is perfectly adapted to its distance. A vertical
line is seen distinctly when the horizontal meridian is adapted to its
distance. It appears indistinct when its image is formed by the vertical
meridian. The way in which an astigmatic person sees points and lines led
to the discovery of this remarkable irregularity in the refraction of the eye.
The late Astronomer Royal, Sir George Airy, suffered for some years until,
indeed, he discovered how it could be corrected. This anomaly of curvature
of the refractive surfaces of the eye is now known to prevail largely among
meridian than in another. Its surfaces then cannot be regarded as entirely
belonging to an ellipsoid of revolution, since the solid figure, of which the
former would constitute a part, has not only two axes, but three, and these
unequal. This irregularity is not, however, always great enough to produce
discomfort and it is therefore disregarded. But in other cases the difference
of curvature in the different meridians of the eye attain to a higher degree,
and vision falls far below the average.
The refractive anomaly alluded to is
termed astigmatism (from the Greek,
α privative, στιγμα, a point—
inability to see a point). The way in
which objects appear to such a
person will mainly result from the
way in which he sees a point. Take,
for example, the vertical to be the
most, and the horizontal to be the
least, refractive meridian: place a
vertical line (Fig. 25, I) at a stated
distance before the eye, and the line
will appear elongated, owing to the
diffusion image of each of the points
Fig. 25.—Lines as seen by the Astigmatic. composing it. It will also seem to be
somewhat broadened, as at II. If the
vertical meridian is adapted to the distance of the vertical, the line will
appear very diffuse and broadened, as at III. All these little diffusion lines
overlap each other, and give the line an elongated appearance. Hence a
straight line is seen distinctly by an astigmatic eye only when the meridian
to which it is perpendicular is perfectly adapted to its distance. A vertical
line is seen distinctly when the horizontal meridian is adapted to its
distance. It appears indistinct when its image is formed by the vertical
meridian. The way in which an astigmatic person sees points and lines led
to the discovery of this remarkable irregularity in the refraction of the eye.
The late Astronomer Royal, Sir George Airy, suffered for some years until,
indeed, he discovered how it could be corrected. This anomaly of curvature
of the refractive surfaces of the eye is now known to prevail largely among
Page 71
the more civilised races of mankind. It is, then, of very great importance
when using high powers of the microscope. In most persons the visual
power of both eyes is rarely quite equal; on the other hand, the mind exerts
an important influence, dominates, as it were, the eye in the interpretation
of visual sensations and images. An example of this is presented in
Wheatstone’s pseudoscope, known to produce precisely the opposite effect
of his stereoscope—conveys, in fact, the converse of relief produced by the
latter and better known instrument.
Visual Judgment.—The apparent size of an object is determined by the
magnitude of the image formed on the retina, and this is inversely
proportional to the distance. Thus the size of an image on the retina of an
object two inches long at a distance of a foot, is equal to the image of an
object four inches long at a distance of two feet. An object can be seen if the
visual angle subtended by it is not less than sixty seconds. This is equivalent
to an image on the fovea centralis of the retina of about 4 µ9 across, and
which corresponds to the diameter of a cone: so that while we have had
under consideration the optical and physical conditions of human vision, we
have likewise taken a lesson on the action of lenses used in the construction
of the microscope.
The Theory of Microscopical Vision.
It has been said that no comparison can be instituted between microscopic
vision and macroscopic; that the images formed by minute objects are not
delineated microscopically under ordinary laws of diffraction, and that the
results are dioptrical. This assertion, however, cannot be accepted
unconditionally, as will be seen on more careful examination of the late
Professor Abbe’s masterly exposition of “The Microscopical Theory of
Vision,” and also his subsequent investigations on the estimation of aperture
and the value of wide-angled immersion objectives, published in the
“Journal of the Royal Microscopical Society.”
The essential point in Abbe’s theory of microscopical vision is that the
images of minute objects in the microscope are not formed exclusively on
the ordinary dioptric method (that is, in the same way in which they are
when using high powers of the microscope. In most persons the visual
power of both eyes is rarely quite equal; on the other hand, the mind exerts
an important influence, dominates, as it were, the eye in the interpretation
of visual sensations and images. An example of this is presented in
Wheatstone’s pseudoscope, known to produce precisely the opposite effect
of his stereoscope—conveys, in fact, the converse of relief produced by the
latter and better known instrument.
Visual Judgment.—The apparent size of an object is determined by the
magnitude of the image formed on the retina, and this is inversely
proportional to the distance. Thus the size of an image on the retina of an
object two inches long at a distance of a foot, is equal to the image of an
object four inches long at a distance of two feet. An object can be seen if the
visual angle subtended by it is not less than sixty seconds. This is equivalent
to an image on the fovea centralis of the retina of about 4 µ9 across, and
which corresponds to the diameter of a cone: so that while we have had
under consideration the optical and physical conditions of human vision, we
have likewise taken a lesson on the action of lenses used in the construction
of the microscope.
The Theory of Microscopical Vision.
It has been said that no comparison can be instituted between microscopic
vision and macroscopic; that the images formed by minute objects are not
delineated microscopically under ordinary laws of diffraction, and that the
results are dioptrical. This assertion, however, cannot be accepted
unconditionally, as will be seen on more careful examination of the late
Professor Abbe’s masterly exposition of “The Microscopical Theory of
Vision,” and also his subsequent investigations on the estimation of aperture
and the value of wide-angled immersion objectives, published in the
“Journal of the Royal Microscopical Society.”
The essential point in Abbe’s theory of microscopical vision is that the
images of minute objects in the microscope are not formed exclusively on
the ordinary dioptric method (that is, in the same way in which they are
Page 72
formed in the camera or telescope), but that they are largely affected by the
peculiar manner in which the minute construction of the object breaks up
the incident rays, giving rise to diffraction.
The phenomena of diffraction in general may be observed experimentally
by plates of glass ruled with fine lines. Fig. 26 shows the appearance
presented by a single candle-flame seen through such a plate, an uncoloured
image of the flame occupying the centre, flanked on either side by a row of
coloured spectra of the flame, which become dimmer as they recede from
the centre. A similar phenomenon may be produced by dust scattered over a
glass plate, and by other objects whose structure contains very minute
particles, or the meshes of very fine gauze wire, the rays suffering a
characteristic change in passing through such objects; that change
consisting in the breaking up of a parallel beam of light into a group of rays,
diverging with wide angle and forming a regular series of maxima and
minima of intensity of light, due to difference of phase of vibration.10
In the same way, in the microscope,
the diffraction pencil originating
from a beam incident upon, for
Fig. 26.
instance, a diatom, appears as a fan
of isolated rays, decreasing in
intensity as they are further removed from the direction of the incident
beam transmitted through the structure, the interference of the primary
waves giving a number of successive maxima of light with dark interspaces.
When a diaphragm opening is interposed between the mirror, and a plate of
ruled lines placed upon the stage such as Fig. 27, the appearance shown in
Fig. 27a, will be observed at the back of the objective on removing the eye-
piece and looking down the tube of the microscope. The centre circles are
the images of the diaphragm opening produced by the direct rays, while
those on the other side (always at right angles to the direction of the lines)
are the diffraction images produced by the rays which are bent off from the
incident pencil. In homogeneous light the central and lateral images agree
in size and form, but in white light the diffraction images are radially drawn
out, with the outer edges red and the inner blue (the reverse of the ordinary
spectrum), forming, in fact, regular spectra the distance separating each of
peculiar manner in which the minute construction of the object breaks up
the incident rays, giving rise to diffraction.
The phenomena of diffraction in general may be observed experimentally
by plates of glass ruled with fine lines. Fig. 26 shows the appearance
presented by a single candle-flame seen through such a plate, an uncoloured
image of the flame occupying the centre, flanked on either side by a row of
coloured spectra of the flame, which become dimmer as they recede from
the centre. A similar phenomenon may be produced by dust scattered over a
glass plate, and by other objects whose structure contains very minute
particles, or the meshes of very fine gauze wire, the rays suffering a
characteristic change in passing through such objects; that change
consisting in the breaking up of a parallel beam of light into a group of rays,
diverging with wide angle and forming a regular series of maxima and
minima of intensity of light, due to difference of phase of vibration.10
In the same way, in the microscope,
the diffraction pencil originating
from a beam incident upon, for
Fig. 26.
instance, a diatom, appears as a fan
of isolated rays, decreasing in
intensity as they are further removed from the direction of the incident
beam transmitted through the structure, the interference of the primary
waves giving a number of successive maxima of light with dark interspaces.
When a diaphragm opening is interposed between the mirror, and a plate of
ruled lines placed upon the stage such as Fig. 27, the appearance shown in
Fig. 27a, will be observed at the back of the objective on removing the eye-
piece and looking down the tube of the microscope. The centre circles are
the images of the diaphragm opening produced by the direct rays, while
those on the other side (always at right angles to the direction of the lines)
are the diffraction images produced by the rays which are bent off from the
incident pencil. In homogeneous light the central and lateral images agree
in size and form, but in white light the diffraction images are radially drawn
out, with the outer edges red and the inner blue (the reverse of the ordinary
spectrum), forming, in fact, regular spectra the distance separating each of
Page 73
which varies inversely as the closeness of the lines, being for instance with
the same objective twice as far apart when the lines are twice as close.
Fig. 27. Fig. 27a.
The influence of these diffraction spectra may be demonstrated by some
very striking experiments, which show that they are not by any means
accidental phenomena, but are directly connected with the image which is
seen by the eye.
The first experiment shows that with the central beam, or any one of the
spectral beams alone, only the contour of the object is seen, the addition of
at least one diffraction spectrum being essential to the visibility of the
structure.
the same objective twice as far apart when the lines are twice as close.
Fig. 27. Fig. 27a.
The influence of these diffraction spectra may be demonstrated by some
very striking experiments, which show that they are not by any means
accidental phenomena, but are directly connected with the image which is
seen by the eye.
The first experiment shows that with the central beam, or any one of the
spectral beams alone, only the contour of the object is seen, the addition of
at least one diffraction spectrum being essential to the visibility of the
structure.
Page 74
Fig. 28. Fig. 28a.
When by a diaphragm placed at the back of the objective, as in Fig. 28, we
cover up all the diffraction spectra of Fig. 27a, and allow only the central
rays to reach the image, the object will appear to be wholly deprived of fine
details, the outline alone will remain, and every delineation of minute
structure will disappear, just as if the microscope had suddenly lost its
optical power, as in Fig. 28a.
This experiment illustrates a case of the obliteration of structure by
obstructing the passage of the diffraction spectra to the eye-piece. The next
experiment shows how the appearance of fine structure may be created by
manipulating the spectra.
Fig. 29. Fig. 29a.
When a diaphragm such as that shown in Fig. 29 is placed at the back of the
objective, so as to cut off each alternate one of the upper row of spectra in
Fig. 27a, that row will obviously become identical with the lower one, and
if the theory holds good, we should find the image of the upper lines
identical with that of the lower. On replacing the eye-piece, we see that it is
When by a diaphragm placed at the back of the objective, as in Fig. 28, we
cover up all the diffraction spectra of Fig. 27a, and allow only the central
rays to reach the image, the object will appear to be wholly deprived of fine
details, the outline alone will remain, and every delineation of minute
structure will disappear, just as if the microscope had suddenly lost its
optical power, as in Fig. 28a.
This experiment illustrates a case of the obliteration of structure by
obstructing the passage of the diffraction spectra to the eye-piece. The next
experiment shows how the appearance of fine structure may be created by
manipulating the spectra.
Fig. 29. Fig. 29a.
When a diaphragm such as that shown in Fig. 29 is placed at the back of the
objective, so as to cut off each alternate one of the upper row of spectra in
Fig. 27a, that row will obviously become identical with the lower one, and
if the theory holds good, we should find the image of the upper lines
identical with that of the lower. On replacing the eye-piece, we see that it is
Page 75
so, the upper set of lines are doubled in number, a new line appearing in the
centre of the space between each of the old (upper) ones, and upper and
lower set having become to all appearance identical, as seen in Fig. 29a.
Fig. 30. Fig. 30a.
In the same way, if we stop off all but the outer spectra, as in Fig. 30, the
lines are apparently again doubled, as seen in Fig. 30a.
A case of apparent creation of structure, similar in principle to the
foregoing, though more striking, is afforded by a network of squares, as in
Fig. 31, having sides parallel to this page, which gives the spectra shown in
Fig. 31a, consisting of vertical rows for the horizontal lines and horizontal
rows for the vertical ones. But it is readily seen that two diagonal rows of
spectra exist at right angles to the diagonals of the squares, just as would
arise from sets of lines in the direction of the diagonals, so that if the theory
holds good we ought to find, on obstructing all the other spectra and
allowing only the diagonal ones to pass to the eye-piece, that the vertical
and horizontal lines have disappeared and are replaced by two new sets of
lines at right angles to the diagonals.
centre of the space between each of the old (upper) ones, and upper and
lower set having become to all appearance identical, as seen in Fig. 29a.
Fig. 30. Fig. 30a.
In the same way, if we stop off all but the outer spectra, as in Fig. 30, the
lines are apparently again doubled, as seen in Fig. 30a.
A case of apparent creation of structure, similar in principle to the
foregoing, though more striking, is afforded by a network of squares, as in
Fig. 31, having sides parallel to this page, which gives the spectra shown in
Fig. 31a, consisting of vertical rows for the horizontal lines and horizontal
rows for the vertical ones. But it is readily seen that two diagonal rows of
spectra exist at right angles to the diagonals of the squares, just as would
arise from sets of lines in the direction of the diagonals, so that if the theory
holds good we ought to find, on obstructing all the other spectra and
allowing only the diagonal ones to pass to the eye-piece, that the vertical
and horizontal lines have disappeared and are replaced by two new sets of
lines at right angles to the diagonals.
Page 76
Fig. 31. Fig. 31a.
Fig. 32. Fig. 32a.
On inserting the diaphragm, Fig. 32, and replacing the eye-piece, we find in
the place of the old network the one shown in Fig. 32a, the squares being,
however, smaller in the proportion of 1 : √2, as they should be in
accordance with the theory propounded.
An object such as Pleurosigma angulatum, which gives six diffraction
spectra arranged as in Fig. 33, should, according to this theory, show
markings in a hexagonal arrangement. For there will be one set of lines at
right angles to b, a, e, another set at right angles to c, a, f, and a third at
right angles to g, a, d. These three sets of lines will obviously produce the
appearance shown in Fig. 33a.
Fig. 33. Fig. 33a.
A great variety of appearances may be produced with the same arrangement
of spectra. Any two adjacent spectra with the central beam (as b, c, a) will
form equilateral triangles and give hexagonal markings. Or by stopping off
all but g, c, e (or b, d, f), we again have the spectra in the form of equilateral
Fig. 32. Fig. 32a.
On inserting the diaphragm, Fig. 32, and replacing the eye-piece, we find in
the place of the old network the one shown in Fig. 32a, the squares being,
however, smaller in the proportion of 1 : √2, as they should be in
accordance with the theory propounded.
An object such as Pleurosigma angulatum, which gives six diffraction
spectra arranged as in Fig. 33, should, according to this theory, show
markings in a hexagonal arrangement. For there will be one set of lines at
right angles to b, a, e, another set at right angles to c, a, f, and a third at
right angles to g, a, d. These three sets of lines will obviously produce the
appearance shown in Fig. 33a.
Fig. 33. Fig. 33a.
A great variety of appearances may be produced with the same arrangement
of spectra. Any two adjacent spectra with the central beam (as b, c, a) will
form equilateral triangles and give hexagonal markings. Or by stopping off
all but g, c, e (or b, d, f), we again have the spectra in the form of equilateral
Page 77
triangles; but as they are now further apart,
the sides of the triangles in the two cases
being as √3 : 1, the hexagons will be
smaller and three times as numerous. Their
sides will also be arranged at a different
angle to those of the first set. The hexagons
may be entirely obliterated by admitting
only the spectra g, c, or g, f, or b, f, etc.,
when new lines will appear at right angles,
or obliquely inclined, to the median line.
By varying the combinations of the spectra,
therefore, different figures of varying size
Fig. 34.
and positions are produced, all of which
cannot, of course, represent the true
structure. Not only, however, may the appearance of particular structure be
obliterated or created, but it may even be predicted before being seen under
the microscope. If the position and relative intensity of the spectra in any
particular case are given, the character of the resultant image, in some
instances, may be worked out by mathematical calculations. A remarkable
instance of such a prediction is to be found in the case recorded by Mr.
Stephenson, where a mathematical student who had never seen a diatom,
worked out the purely mathematical result of the interference of the six
spectra b-g of Fig. 33 (identical with P. angulatum), giving the drawing
copied in Fig. 34. The special feature was the small markings between the
hexagons, which had not, before this time, been noticed on P. angulatum.
On more closely scrutinizing a valve, stopping out the central beam and
allowing the six spectra only to pass, the small markings were found
actually to exist, though they were so faint they had previously escaped
observation until the result of the mathematical deduction had shown that
they ought to be seen.
These experiments seem to show that diffraction plays a very essential part
in the formation of microscopical images, since dissimilar structures give
identical images when the differences of their diffractive effect is removed,
and conversely similar structures may give dissimilar images when their
diffractive images are made dissimilar. Whilst a purely dioptric image
answers point for point to the object on the stage, and enables a safe
the sides of the triangles in the two cases
being as √3 : 1, the hexagons will be
smaller and three times as numerous. Their
sides will also be arranged at a different
angle to those of the first set. The hexagons
may be entirely obliterated by admitting
only the spectra g, c, or g, f, or b, f, etc.,
when new lines will appear at right angles,
or obliquely inclined, to the median line.
By varying the combinations of the spectra,
therefore, different figures of varying size
Fig. 34.
and positions are produced, all of which
cannot, of course, represent the true
structure. Not only, however, may the appearance of particular structure be
obliterated or created, but it may even be predicted before being seen under
the microscope. If the position and relative intensity of the spectra in any
particular case are given, the character of the resultant image, in some
instances, may be worked out by mathematical calculations. A remarkable
instance of such a prediction is to be found in the case recorded by Mr.
Stephenson, where a mathematical student who had never seen a diatom,
worked out the purely mathematical result of the interference of the six
spectra b-g of Fig. 33 (identical with P. angulatum), giving the drawing
copied in Fig. 34. The special feature was the small markings between the
hexagons, which had not, before this time, been noticed on P. angulatum.
On more closely scrutinizing a valve, stopping out the central beam and
allowing the six spectra only to pass, the small markings were found
actually to exist, though they were so faint they had previously escaped
observation until the result of the mathematical deduction had shown that
they ought to be seen.
These experiments seem to show that diffraction plays a very essential part
in the formation of microscopical images, since dissimilar structures give
identical images when the differences of their diffractive effect is removed,
and conversely similar structures may give dissimilar images when their
diffractive images are made dissimilar. Whilst a purely dioptric image
answers point for point to the object on the stage, and enables a safe
Page 78
inference to be drawn as to the actual nature of that object, the visible
indications of minute structure in a microscopical image are not always or
necessarily conformable to the real nature of the object examined, so that
nothing more can safely be inferred from the image as presented to the eye,
than the presence in the object of such structural peculiarities as will
produce the particular diffraction phenomena on which these images
depend.
Further investigations and experiments led Abbe to discard so much of his
theoretical conclusions relating to superimposed images having a distinct
character as well as a different origin, and as to their capability of being
separated and examined apart from each other. In a later paper he writes: “I
no longer maintain in principle the distinction between the absorption
image or direct dioptrical image and the diffraction image, nor do I hold
that the microscopical image of an object consists of two superimposed
images of different origin or a different mode of production. Thus it appears
that both the absorption image and the diffraction image he held to be
equally of diffraction origin; but while a lens of small aperture would give
the former with facility, it would be powerless to reveal the latter, because
of its limited capacity to gather in the strongly-deflected rays due to the
excessively minute bodies the microscopical objective has to deal with.”11
Abbe’s theory of vision has been questioned by mathematicians, and since
his death Lord Rayleigh went more deeply into the question of “the theory
of the formation of optical images,” with special reference to the
microscope and telescope. He has shown that two lines cannot be fairly
resolved unless their components subtend an angle exceeding that
subtended by the wave-length of light at a distance equal to the aperture;
also, that the measure of resolution is only possible with a square aperture,
or one bounded by straight lines, parallel to the lines resolved.
Lord Rayleigh’s Theory of the Formation of Optical Images, with
Special Reference to the Microscope.12
Of the two methods adopted, that of Helmholtz’s consists in tracing the
image representative of a mathematical point in the object, the point being
indications of minute structure in a microscopical image are not always or
necessarily conformable to the real nature of the object examined, so that
nothing more can safely be inferred from the image as presented to the eye,
than the presence in the object of such structural peculiarities as will
produce the particular diffraction phenomena on which these images
depend.
Further investigations and experiments led Abbe to discard so much of his
theoretical conclusions relating to superimposed images having a distinct
character as well as a different origin, and as to their capability of being
separated and examined apart from each other. In a later paper he writes: “I
no longer maintain in principle the distinction between the absorption
image or direct dioptrical image and the diffraction image, nor do I hold
that the microscopical image of an object consists of two superimposed
images of different origin or a different mode of production. Thus it appears
that both the absorption image and the diffraction image he held to be
equally of diffraction origin; but while a lens of small aperture would give
the former with facility, it would be powerless to reveal the latter, because
of its limited capacity to gather in the strongly-deflected rays due to the
excessively minute bodies the microscopical objective has to deal with.”11
Abbe’s theory of vision has been questioned by mathematicians, and since
his death Lord Rayleigh went more deeply into the question of “the theory
of the formation of optical images,” with special reference to the
microscope and telescope. He has shown that two lines cannot be fairly
resolved unless their components subtend an angle exceeding that
subtended by the wave-length of light at a distance equal to the aperture;
also, that the measure of resolution is only possible with a square aperture,
or one bounded by straight lines, parallel to the lines resolved.
Lord Rayleigh’s Theory of the Formation of Optical Images, with
Special Reference to the Microscope.12
Of the two methods adopted, that of Helmholtz’s consists in tracing the
image representative of a mathematical point in the object, the point being
Page 79
regarded as self-luminous; that of Abbe’s the typical object was not, as we
have seen, a luminous point, but a grating illuminated by plane waves of
light. In the latter method, Lord Rayleigh argues that the complete
representation of the object requires the co-operation of all the spectra
which are focussed in the principal focal plane of the objective; when only a
few are present the representation is imperfect, and wholly fails when there
is only one. He then proceeds to show, by the aid of diagrams and
mathematical formula, how the resolving power can be adduced.
On further criticism of the Abbe spectrum theory, he observes “that
although the image ultimately formed may be considered to be due to the
spectra focussed to a given point, the degree of conformity of the image to
the object is another question. The consideration of the case of a very fine
grating, which might afford no lateral spectra at all, shows the incorrectness
of the usually accepted idea that if all the spectra are utilised the image will
still be incomplete, so that the theory (originally promulgated by Abbe)
requires a good deal of supplementing; while it is inapplicable when the
incident light is not parallel, and when the object is, for example, a double
point and not a grating. Even in the case of a grating, the spectrum theory is
inapplicable, if the grating is self-luminous; for in this case no spectra can
be formed since the radiations from the different elements of the grating
have no permanent phase-relations.” For these reasons Lord Rayleigh
advises that the question should be reconsidered from the older point of
view, according to which the typical object is a point and not a grating.
Such treatment will show that the theory of resolving power is essentially
the same for all instruments. The peculiarities of the microscope, arising
from the divergence-angles not being limited to be small, and from the
different character of the illumination, are theoretically only differences of
detail. These investigations can be extended to gratings, and the results so
obtained confirm for the most part the conclusions of the spectrum theory.
Furthermore, that the function of the condenser in microscopic practice in
throwing upon the object the image of the lamp-flame is to cause the object
to behave, at any rate in some degree, as if it were self-luminous, and thus
to obviate the sharply-marked interference bands which arise when
permanent and definite phase-relations are permitted to exist between the
radiations which issue from various points of the object. This is capable of
have seen, a luminous point, but a grating illuminated by plane waves of
light. In the latter method, Lord Rayleigh argues that the complete
representation of the object requires the co-operation of all the spectra
which are focussed in the principal focal plane of the objective; when only a
few are present the representation is imperfect, and wholly fails when there
is only one. He then proceeds to show, by the aid of diagrams and
mathematical formula, how the resolving power can be adduced.
On further criticism of the Abbe spectrum theory, he observes “that
although the image ultimately formed may be considered to be due to the
spectra focussed to a given point, the degree of conformity of the image to
the object is another question. The consideration of the case of a very fine
grating, which might afford no lateral spectra at all, shows the incorrectness
of the usually accepted idea that if all the spectra are utilised the image will
still be incomplete, so that the theory (originally promulgated by Abbe)
requires a good deal of supplementing; while it is inapplicable when the
incident light is not parallel, and when the object is, for example, a double
point and not a grating. Even in the case of a grating, the spectrum theory is
inapplicable, if the grating is self-luminous; for in this case no spectra can
be formed since the radiations from the different elements of the grating
have no permanent phase-relations.” For these reasons Lord Rayleigh
advises that the question should be reconsidered from the older point of
view, according to which the typical object is a point and not a grating.
Such treatment will show that the theory of resolving power is essentially
the same for all instruments. The peculiarities of the microscope, arising
from the divergence-angles not being limited to be small, and from the
different character of the illumination, are theoretically only differences of
detail. These investigations can be extended to gratings, and the results so
obtained confirm for the most part the conclusions of the spectrum theory.
Furthermore, that the function of the condenser in microscopic practice in
throwing upon the object the image of the lamp-flame is to cause the object
to behave, at any rate in some degree, as if it were self-luminous, and thus
to obviate the sharply-marked interference bands which arise when
permanent and definite phase-relations are permitted to exist between the
radiations which issue from various points of the object. This is capable of
Page 80
mathematical proof; and in the case where the illumination is such that each
point of the row or of the grating radiates independently, the limit to
resolution is seen to depend only on the width of the aperture, and thus to
be the same for all forms of aperture as for those of the rectangular. That
Abbe’s theory of microscopic vision is fairly open to the criticisms passed
on it by Lord Rayleigh must be taken for granted.
Definition of Aperture; Principles of Microscopic Vision.
It must be well within the last half-century that the achromatic objective-
glass for the microscope was brought to perfection and its value became
generally recognised. Prior to the discovery of the achromatic principle in
the construction of lenses it was assumed that the formation of the
microscopic image took place (as we have already seen) on ordinary
dioptric principles. As the image is formed in the camera or telescope, so it
was said to be in the microscope. This belief existed, it will be remembered,
at a time when dry objectives only were in favour and the use of the term
angle of aperture was misunderstood, when it was supposed that the
different media with diffraction-indices were used; and the angle of the
radiant pencil was believed not only to admit of a comparison of two
apertures in the same medium, but likewise to admit of a standard of
comparison when the media were entirely different in their refractive
qualities.
It was during my tenure of office as secretary of the Royal Microscopical
Society (1867 to 1873), that the aperture question, and also that of
numerical aperture, came under discussion, both being met by the majority
of the Fellows of the Society and practical opticians by a non-possumus.
Opticians alleged, that is, before the value of aperture became fully
recognised (1860), that the achromatic objective had reached a stage of
perfection, beyond which it was not possible to go; indeed, not only
opticians, but physicists of high standing, as Professor Helmholtz, who
made many important contributions to the theory of the microscope, and
who, after duly weighing all the known physical laws on which the
formation of images can be explained, emphatically stated that in his
point of the row or of the grating radiates independently, the limit to
resolution is seen to depend only on the width of the aperture, and thus to
be the same for all forms of aperture as for those of the rectangular. That
Abbe’s theory of microscopic vision is fairly open to the criticisms passed
on it by Lord Rayleigh must be taken for granted.
Definition of Aperture; Principles of Microscopic Vision.
It must be well within the last half-century that the achromatic objective-
glass for the microscope was brought to perfection and its value became
generally recognised. Prior to the discovery of the achromatic principle in
the construction of lenses it was assumed that the formation of the
microscopic image took place (as we have already seen) on ordinary
dioptric principles. As the image is formed in the camera or telescope, so it
was said to be in the microscope. This belief existed, it will be remembered,
at a time when dry objectives only were in favour and the use of the term
angle of aperture was misunderstood, when it was supposed that the
different media with diffraction-indices were used; and the angle of the
radiant pencil was believed not only to admit of a comparison of two
apertures in the same medium, but likewise to admit of a standard of
comparison when the media were entirely different in their refractive
qualities.
It was during my tenure of office as secretary of the Royal Microscopical
Society (1867 to 1873), that the aperture question, and also that of
numerical aperture, came under discussion, both being met by the majority
of the Fellows of the Society and practical opticians by a non-possumus.
Opticians alleged, that is, before the value of aperture became fully
recognised (1860), that the achromatic objective had reached a stage of
perfection, beyond which it was not possible to go; indeed, not only
opticians, but physicists of high standing, as Professor Helmholtz, who
made many important contributions to the theory of the microscope, and
who, after duly weighing all the known physical laws on which the
formation of images can be explained, emphatically stated that in his
Page 81
opinion “the limit of possible improvement of the microscope as an
instrument of discovery had been very nearly reached.” A quarter of a
century ago I ventured to throw a doubt upon so questionable a statement. I
determined, if possible, to submit the aperture question to an exhaustive
examination. My views were accordingly submitted to two of the highest
authorities in this country—Sir George Airy, the then Astronomer Royal,
and Sir George Stokes, Professor of Physics at Cambridge University—both
of whom agreed with me that the possible increase of aperture would be
attended with great advantage to the objective, and open the way to an
extension of power resolution in the microscope.13 The discussion
afterwards took a warm turn, as will be seen on reference to “The Monthly
Microscopical Journals” of 1874, 1875 and 1876.
The confusion into which the aperture question at this period had lapsed
was no doubt due to the fact that its opponents had not yet grasped the true
meaning of the term aperture. It was believed to be synonymous with
“angular aperture,” much in use at the time. It will, however, appear quite
unaccountable that even the older opticians should have confounded the
latter with the former; and so entirely disregarded the fact that the angles of
the pencil of light admitted by the objective cannot serve as a measure of its
aperture, and that high refractive media can greatly reduce the value length
of waves of light.
When the medium in which the objective works is the same as air, it is not
that a comparison can be made by the angles of the radiant pencils only, but
by their sines. For example, if two dry objectives admit pencils of 60° and
180°, their real apertures are not as 1 : 3, but as 1 : 2 only. Aperture in fact
is computed by mathematicians by tracing the rays from the back focus
through the system of lenses to the front focus, the front focus being the
point at which the whole cone of rays converge as free as may be from
aberration. If the front focus be in air, no pencil greater than 82°, “double
the angle of total reflection,” can emerge from the plane front of the lens;
and, obviously, if no greater cone can emerge to a focus one way, neither
can any greater cone enter the body of the lens from the radiant. This angle,
then, of 82°, must be regarded as the limit for dry lenses or objectives.
instrument of discovery had been very nearly reached.” A quarter of a
century ago I ventured to throw a doubt upon so questionable a statement. I
determined, if possible, to submit the aperture question to an exhaustive
examination. My views were accordingly submitted to two of the highest
authorities in this country—Sir George Airy, the then Astronomer Royal,
and Sir George Stokes, Professor of Physics at Cambridge University—both
of whom agreed with me that the possible increase of aperture would be
attended with great advantage to the objective, and open the way to an
extension of power resolution in the microscope.13 The discussion
afterwards took a warm turn, as will be seen on reference to “The Monthly
Microscopical Journals” of 1874, 1875 and 1876.
The confusion into which the aperture question at this period had lapsed
was no doubt due to the fact that its opponents had not yet grasped the true
meaning of the term aperture. It was believed to be synonymous with
“angular aperture,” much in use at the time. It will, however, appear quite
unaccountable that even the older opticians should have confounded the
latter with the former; and so entirely disregarded the fact that the angles of
the pencil of light admitted by the objective cannot serve as a measure of its
aperture, and that high refractive media can greatly reduce the value length
of waves of light.
When the medium in which the objective works is the same as air, it is not
that a comparison can be made by the angles of the radiant pencils only, but
by their sines. For example, if two dry objectives admit pencils of 60° and
180°, their real apertures are not as 1 : 3, but as 1 : 2 only. Aperture in fact
is computed by mathematicians by tracing the rays from the back focus
through the system of lenses to the front focus, the front focus being the
point at which the whole cone of rays converge as free as may be from
aberration. If the front focus be in air, no pencil greater than 82°, “double
the angle of total reflection,” can emerge from the plane front of the lens;
and, obviously, if no greater cone can emerge to a focus one way, neither
can any greater cone enter the body of the lens from the radiant. This angle,
then, of 82°, must be regarded as the limit for dry lenses or objectives.
Page 82
This limit, it will be seen on more careful examination, is very nearly the
maximum angle that can be computed for a lens to have a front focus in air.
This can be proved by the consideration of the angle of the image of rays,
as they are radiated from the object itself in balsam: for although this angle
of image rays viewed as nascent from a self-luminous object capable of
scattering rays in all directions, may be 180° in the substance of the balsam
and cover-glass, of the 180° only 82° of the central portion will emerge into
air—all rays beyond this limit are internally reflected at the cover-glass.
This cone, then, of 82° becomes 180° in air, and a large part must
necessarily be lost by reflection at the first incidence on the plane front of
the lens. But with a formula permitting the use of a water medium between
the front lens and the cover-glass, the aperture of the image rays may reach
126°—double the critical angle from glass to water; and with an oil
medium, the aperture will be found to be limited only by the form of the
front lens that can be constructed by the optician.
To sum up, then, the effect of the immersion system, greatly assists in the
correction of aberration, gives increased magnification and angular
aperture, increase of working distance between the objective and object,
and renders admissible the use of the thicker glass-cover.
The aperture question would in all probability have remained unsolved
many years longer (ten or twelve years elapsed after I brought the question
under discussion before opticians gave way), but for the fortunate
circumstance that the eminent mathematical and practical optician,
Professor Abbe, of Jena, was about to visit London. This came off in the
early part of the seventies, when the late Mr. John Mayall and myself had
the good fortune to interview him. The subject discussed was naturally the
increase of aperture and the theory of microscopical vision. He readily at
our request undertook to re-investigate the question in all its bearings on the
microscope. It is almost unnecessary to add that the conclusions he came to,
and the results obtained, have proved of inestimable value to the
microscopist and practical optician, and it may well seem necessary to
explain somewhat at greater length the conclusions the learned Professor
came to, and by the adoption of which the microscope has been placed on a
more scientific basis than it had before attained to. Several papers were
published in extenso in the “Journal of the Royal Microscopical Society,”
maximum angle that can be computed for a lens to have a front focus in air.
This can be proved by the consideration of the angle of the image of rays,
as they are radiated from the object itself in balsam: for although this angle
of image rays viewed as nascent from a self-luminous object capable of
scattering rays in all directions, may be 180° in the substance of the balsam
and cover-glass, of the 180° only 82° of the central portion will emerge into
air—all rays beyond this limit are internally reflected at the cover-glass.
This cone, then, of 82° becomes 180° in air, and a large part must
necessarily be lost by reflection at the first incidence on the plane front of
the lens. But with a formula permitting the use of a water medium between
the front lens and the cover-glass, the aperture of the image rays may reach
126°—double the critical angle from glass to water; and with an oil
medium, the aperture will be found to be limited only by the form of the
front lens that can be constructed by the optician.
To sum up, then, the effect of the immersion system, greatly assists in the
correction of aberration, gives increased magnification and angular
aperture, increase of working distance between the objective and object,
and renders admissible the use of the thicker glass-cover.
The aperture question would in all probability have remained unsolved
many years longer (ten or twelve years elapsed after I brought the question
under discussion before opticians gave way), but for the fortunate
circumstance that the eminent mathematical and practical optician,
Professor Abbe, of Jena, was about to visit London. This came off in the
early part of the seventies, when the late Mr. John Mayall and myself had
the good fortune to interview him. The subject discussed was naturally the
increase of aperture and the theory of microscopical vision. He readily at
our request undertook to re-investigate the question in all its bearings on the
microscope. It is almost unnecessary to add that the conclusions he came to,
and the results obtained, have proved of inestimable value to the
microscopist and practical optician, and it may well seem necessary to
explain somewhat at greater length the conclusions the learned Professor
came to, and by the adoption of which the microscope has been placed on a
more scientific basis than it had before attained to. Several papers were
published in extenso in the “Journal of the Royal Microscopical Society,”
Page 83
and I am greatly indebted to Mr. Frank Crisp, LL.D., for an excellent
resumé of Abbe’s Monograph.14
The essential step in the consideration of aperture is, as I have said, to
understand clearly what is meant by the term. It will at once be recognised
that its definition must necessarily refer to its primary meaning of opening,
and must, in the case of an optical instrument, define its capacity for
receiving rays from the object, and transmitting them to the image received
at the eye-piece.
In the case of the telescope-objective, its capacity for receiving and
transmitting rays is necessarily measured by the expression of its absolute
diameter or “opening.” No such absolute measure can be applied in the case
of the microscope objective, the largest constructed lenses of which having
by no means the largest apertures, being, in fact, the lower powers of the
instrument, whose apertures are for the most part but small. The capacity of
a microscope objective for receiving and transmitting rays is, however, as
will be seen, estimated by its relative opening, that is, its opening in relation
to its focal length. When this relative opening has been ascertained, it may
be regarded as synonymous with that denoted in the telescope by absolute
opening. That this is so will be better appreciated by the following
consideration:—
In a single lens, the rays admitted within one meridional plane evidently
increase as the diameter of the lens (all other circumstances remaining the
same), and in the microscope we have, at the back of the lens, the same
conditions to deal with as are in front in the case of the telescope; the larger
or smaller number of emergent rays will therefore be measured by the clear
diameter, and as no rays can emerge that have not first been admitted, this
will give the measure of the admitted rays under similar circumstances.
If the lenses compared have different focal lengths but the same clear
“openings,” they will transmit the same number of rays to equal areas of an
image at a definite distance, because they would admit the same number if
an object were substituted for the image; that is, if the lens were used as a
telescope-objective. But as the focal lengths are different, the amplification
of the images is different also, and equal areas of these images correspond
to different areas of the object from which the rays are collected. Therefore,
resumé of Abbe’s Monograph.14
The essential step in the consideration of aperture is, as I have said, to
understand clearly what is meant by the term. It will at once be recognised
that its definition must necessarily refer to its primary meaning of opening,
and must, in the case of an optical instrument, define its capacity for
receiving rays from the object, and transmitting them to the image received
at the eye-piece.
In the case of the telescope-objective, its capacity for receiving and
transmitting rays is necessarily measured by the expression of its absolute
diameter or “opening.” No such absolute measure can be applied in the case
of the microscope objective, the largest constructed lenses of which having
by no means the largest apertures, being, in fact, the lower powers of the
instrument, whose apertures are for the most part but small. The capacity of
a microscope objective for receiving and transmitting rays is, however, as
will be seen, estimated by its relative opening, that is, its opening in relation
to its focal length. When this relative opening has been ascertained, it may
be regarded as synonymous with that denoted in the telescope by absolute
opening. That this is so will be better appreciated by the following
consideration:—
In a single lens, the rays admitted within one meridional plane evidently
increase as the diameter of the lens (all other circumstances remaining the
same), and in the microscope we have, at the back of the lens, the same
conditions to deal with as are in front in the case of the telescope; the larger
or smaller number of emergent rays will therefore be measured by the clear
diameter, and as no rays can emerge that have not first been admitted, this
will give the measure of the admitted rays under similar circumstances.
If the lenses compared have different focal lengths but the same clear
“openings,” they will transmit the same number of rays to equal areas of an
image at a definite distance, because they would admit the same number if
an object were substituted for the image; that is, if the lens were used as a
telescope-objective. But as the focal lengths are different, the amplification
of the images is different also, and equal areas of these images correspond
to different areas of the object from which the rays are collected. Therefore,
Page 84
the higher power lens with the same opening as the lower power, will admit
a greater number of rays in all from the same object, because it admits the
same number as the latter from a smaller portion of the object. Thus, if the
focal lengths of two lenses are as 2 : 1, and the first amplifies N diameters,
the second will amplify 2 N with the same distance of the image, so that the
rays which are collected to a given field of 1 mm. diameter of the image are
admitted from a field of 1/N mm. in the first case, and of 1/2N mm. in the
second. As the “opening” of the objective is estimated by the diameter (and
not by the area) the higher power lens admits twice as many rays as the
lower power, because it admits the same number from a field of half the
diameter, and, in general, the admission of rays by the same opening, but
different powers, must be in the inverse ratio of the focal lengths.
In the case of the single lens, therefore, its aperture is determined by the
ratio between the clear opening and the focal length. The same
considerations apply to the case of a compound objective, substituting,
however, for the clear opening of the single lens the diameter of the pencil
at its emergence from the objective, that is, the clear utilised diameter of the
back lens. All equally holds good whether the medium in which the
objective is placed is the same in the case of the two objectives or different,
as an alteration of the medium makes no difference in the power.
180° Oil Angle. (Numerical
Aperture 1·52.)
180° Water Angle. (Numerical
Aperture 1·33.)
a greater number of rays in all from the same object, because it admits the
same number as the latter from a smaller portion of the object. Thus, if the
focal lengths of two lenses are as 2 : 1, and the first amplifies N diameters,
the second will amplify 2 N with the same distance of the image, so that the
rays which are collected to a given field of 1 mm. diameter of the image are
admitted from a field of 1/N mm. in the first case, and of 1/2N mm. in the
second. As the “opening” of the objective is estimated by the diameter (and
not by the area) the higher power lens admits twice as many rays as the
lower power, because it admits the same number from a field of half the
diameter, and, in general, the admission of rays by the same opening, but
different powers, must be in the inverse ratio of the focal lengths.
In the case of the single lens, therefore, its aperture is determined by the
ratio between the clear opening and the focal length. The same
considerations apply to the case of a compound objective, substituting,
however, for the clear opening of the single lens the diameter of the pencil
at its emergence from the objective, that is, the clear utilised diameter of the
back lens. All equally holds good whether the medium in which the
objective is placed is the same in the case of the two objectives or different,
as an alteration of the medium makes no difference in the power.
180° Oil Angle. (Numerical
Aperture 1·52.)
180° Water Angle. (Numerical
Aperture 1·33.)
Page 85
180° Air Angle. 96° Water Angle.
82° Oil Angle. (Numerical Aperture
1·00.)
97° Air Angle. (Numerical Aperture
·75.)
60° Air Angle. (Numerical Aperture
·50.)
Fig. 35.—Relative diameters of the (utilized) back lenses of various dry and
immersion objectives of the same power (¼-in.) from an air angle of 60° to an
oil angle of 180°.
Thus we arrive at a general proposition for all kinds of objectives: 1st, when
the power is the same, the admission of rays (or aperture) varies with the
diameter of the pencil at its emergence; 2nd, when the powers are different,
the same aperture requires different openings in the ratio of the focal
lengths, or conversely with the same opening the aperture is in inverse ratio
to the focal lengths. We see, therefore, that just as in the telescope the
absolute diameter of the object-glass defines its aperture, so in the
microscope the ratio between the utilised diameter of the back lens and the
focal length of the objective defines its aperture also, and this is clearly a
definition of aperture in its primary and only legitimate meaning as
“opening;” that is, the capacity of the objective for admitting rays from the
object and transmitting them to the image.
If, by way of illustration, we compare a series of dry and oil-immersion
objectives, and commencing with small air angles, progress up to 180° air
angle, and then take an oil-immersion of 82° and progress again to 180° oil
angle, the ratio of opening to power progresses also, and attains its
maximum, not in the case of the air angle of 180° (when it is exactly
equivalent to the oil angle of only 82°), but is greatest at the oil angle of
180°. If we assume the objectives to have the same power throughout we
get rid of one of the factors of the ratio, and we have only to compare the
diameters of the emergent beams, and can represent their relations by
diagrams.
82° Oil Angle. (Numerical Aperture
1·00.)
97° Air Angle. (Numerical Aperture
·75.)
60° Air Angle. (Numerical Aperture
·50.)
Fig. 35.—Relative diameters of the (utilized) back lenses of various dry and
immersion objectives of the same power (¼-in.) from an air angle of 60° to an
oil angle of 180°.
Thus we arrive at a general proposition for all kinds of objectives: 1st, when
the power is the same, the admission of rays (or aperture) varies with the
diameter of the pencil at its emergence; 2nd, when the powers are different,
the same aperture requires different openings in the ratio of the focal
lengths, or conversely with the same opening the aperture is in inverse ratio
to the focal lengths. We see, therefore, that just as in the telescope the
absolute diameter of the object-glass defines its aperture, so in the
microscope the ratio between the utilised diameter of the back lens and the
focal length of the objective defines its aperture also, and this is clearly a
definition of aperture in its primary and only legitimate meaning as
“opening;” that is, the capacity of the objective for admitting rays from the
object and transmitting them to the image.
If, by way of illustration, we compare a series of dry and oil-immersion
objectives, and commencing with small air angles, progress up to 180° air
angle, and then take an oil-immersion of 82° and progress again to 180° oil
angle, the ratio of opening to power progresses also, and attains its
maximum, not in the case of the air angle of 180° (when it is exactly
equivalent to the oil angle of only 82°), but is greatest at the oil angle of
180°. If we assume the objectives to have the same power throughout we
get rid of one of the factors of the ratio, and we have only to compare the
diameters of the emergent beams, and can represent their relations by
diagrams.
Page 86
Fig. 35 illustrates five cases of different apertures of ¼-in. objectives, viz.:
those of dry objectives of 60°, 97°, and 180° air angle, a water-immersion
of 180° water angle, and an oil-immersion of 180° oil angle. The inner
dotted circles in the two latter cases are of the same size as that
corresponding to the 180° air angle.
A dry objective of the maximum air angle of 180° is only able to utilise a
diameter of back lens equal to twice the focal length, while an immersion
lens of even only 100° utilises a larger diameter, i.e., it is able to transmit
more rays from the object to the image than any dry objective is capable of
transmitting. Whenever the angle of an immersion lens exceeds twice the
critical angle for the immersion fluid, i.e., 96° for water or 82° for oil, its
aperture is in excess of that of a dry objective of 180°.
Fig. 36.
This excess will be seen if we take an oil-immersion objective of, say 122°
balsam angle, illuminating it so that the whole field is filled with the
incident rays, and use it first on an object not mounted in balsam, but dry.
We then have a dry objective of nearly 180° angular aperture, for, as will be
seen by reference to Fig. 36, the cover-glass is virtually the first surface of
the objective, as the front lens, the immersion fluid, and the cover-glass are
all approximately of the same index, and form, therefore, a front lens of
extra thickness. When the object is close to the cover-glass the pencil
radiating from it will be very nearly 180°, and the emergent pencil
(observed by removing the eye-piece) will be seen to utilise as much of the
those of dry objectives of 60°, 97°, and 180° air angle, a water-immersion
of 180° water angle, and an oil-immersion of 180° oil angle. The inner
dotted circles in the two latter cases are of the same size as that
corresponding to the 180° air angle.
A dry objective of the maximum air angle of 180° is only able to utilise a
diameter of back lens equal to twice the focal length, while an immersion
lens of even only 100° utilises a larger diameter, i.e., it is able to transmit
more rays from the object to the image than any dry objective is capable of
transmitting. Whenever the angle of an immersion lens exceeds twice the
critical angle for the immersion fluid, i.e., 96° for water or 82° for oil, its
aperture is in excess of that of a dry objective of 180°.
Fig. 36.
This excess will be seen if we take an oil-immersion objective of, say 122°
balsam angle, illuminating it so that the whole field is filled with the
incident rays, and use it first on an object not mounted in balsam, but dry.
We then have a dry objective of nearly 180° angular aperture, for, as will be
seen by reference to Fig. 36, the cover-glass is virtually the first surface of
the objective, as the front lens, the immersion fluid, and the cover-glass are
all approximately of the same index, and form, therefore, a front lens of
extra thickness. When the object is close to the cover-glass the pencil
radiating from it will be very nearly 180°, and the emergent pencil
(observed by removing the eye-piece) will be seen to utilise as much of the
Page 87
back lens of the objective as is equal to twice the focal length, that is, the
inner of the two circles at the head of Fig. 35.
If now balsam be run in beneath the cover-glass so that the angle of the
pencil taken up by the objective is no longer 180°, but 122° only (that is,
smaller), the diameter of the emergent pencil is larger than it was before,
when the angle of the pencil was 180° in air, and will be approximately
represented by the outer circle of Fig. 35. As the power remains the same in
both cases, the larger diameter denotes the greater aperture of the
immersion objective over a dry objective of even 180° angle, and the excess
of aperture is made plainly visible.
Having settled the principle, it is still necessary, however, to find a proper
notation for comparing apertures. The astronomer can compare the
apertures of his various objectives by simply expressing them in inches, but
this is obviously not available to the microscopist, who has to deal with the
ratio of two varying quantities.
In consequence of a discovery made by Professor Abbe in 1873, that a
general relation existed between the pencil admitted into the front of the
objective and that emerging from the back of the objective, he was able to
show that the ratio of the semi-diameter of the emergent pencil to the focal
length of the objective could be expressed by the formula n Sin u, i.e., by
the sine of half the angle of aperture (u) multiplied by the refractive index
of the medium (n) in front of the objective (n being 1·0 for air, 1·33 for
water, and 1·52 for oil or balsam).
When, then, the values in any given cases of the expression n Sin u (which
is known as the “numerical aperture”) has been ascertained, the objectives
are instantly compared as regards their aperture, and, moreover, as 180° in
air is equal to 1·0 (since n = 1·0 and the sine of half 180° = 1·0) we see,
with equal readiness, whether the aperture is smaller or larger than that
corresponding to 180° in air. Thus, suppose we desire to compare the
apertures of three objectives, one a dry objective, the second a water
immersion, and the third an oil immersion; these would be compared on the
angular aperture view as, say 74° air angle, 85° water angle, and 118° oil
angle, so that a calculation must be worked out to arrive at the actual
relation between them. Applying, however, the numerical15 notation, which
inner of the two circles at the head of Fig. 35.
If now balsam be run in beneath the cover-glass so that the angle of the
pencil taken up by the objective is no longer 180°, but 122° only (that is,
smaller), the diameter of the emergent pencil is larger than it was before,
when the angle of the pencil was 180° in air, and will be approximately
represented by the outer circle of Fig. 35. As the power remains the same in
both cases, the larger diameter denotes the greater aperture of the
immersion objective over a dry objective of even 180° angle, and the excess
of aperture is made plainly visible.
Having settled the principle, it is still necessary, however, to find a proper
notation for comparing apertures. The astronomer can compare the
apertures of his various objectives by simply expressing them in inches, but
this is obviously not available to the microscopist, who has to deal with the
ratio of two varying quantities.
In consequence of a discovery made by Professor Abbe in 1873, that a
general relation existed between the pencil admitted into the front of the
objective and that emerging from the back of the objective, he was able to
show that the ratio of the semi-diameter of the emergent pencil to the focal
length of the objective could be expressed by the formula n Sin u, i.e., by
the sine of half the angle of aperture (u) multiplied by the refractive index
of the medium (n) in front of the objective (n being 1·0 for air, 1·33 for
water, and 1·52 for oil or balsam).
When, then, the values in any given cases of the expression n Sin u (which
is known as the “numerical aperture”) has been ascertained, the objectives
are instantly compared as regards their aperture, and, moreover, as 180° in
air is equal to 1·0 (since n = 1·0 and the sine of half 180° = 1·0) we see,
with equal readiness, whether the aperture is smaller or larger than that
corresponding to 180° in air. Thus, suppose we desire to compare the
apertures of three objectives, one a dry objective, the second a water
immersion, and the third an oil immersion; these would be compared on the
angular aperture view as, say 74° air angle, 85° water angle, and 118° oil
angle, so that a calculation must be worked out to arrive at the actual
relation between them. Applying, however, the numerical15 notation, which
Page 88
gives ·60 for the dry objective, ·90 for the water immersion, and 1·30 for
the oil immersion, their relative apertures are immediately recognised, and
it is seen, for instance, that the aperture of the water immersion is somewhat
less than that of a dry objective of 180°, and that the aperture of the oil
immersion exceeds that of the latter by 30%.
The advantage of immersion, in comparison with dry objectives, becomes
at once apparent. Instead of consisting merely in a diminution of the loss of
light by reflection or increased working distance, it is seen that a wide-
angled immersion objective has a larger aperture than a dry objective of
maximum angle, so that for any of the purposes for which aperture is
essential an immersion must necessarily be preferred to a dry objective.
That pencils of identical angular extension but in different media are
different physically, will cease to appear in any way paradoxical if we recall
the simple optical fact that rays, which in air are spread out over the whole
hemisphere, are in a medium of higher refractive index such as oil
compressed into a cone of 82° round the perpendicular, i.e., twice the
critical angle. A cone exceeding twice the critical angle of the medium will
therefore embrace a surplus of rays which do not exist even in the
hemisphere when the object is in air.
The whole aperture question, notwithstanding the innumerable perplexities
which heretofore surrounded it, is in reality completely solved by these two
simple considerations: First, that “aperture” is to be applied in its ordinary
meaning as representing the greater or less capacity of the objective for
receiving and transmitting rays; and second, that when so applied the
aperture of an objective is determined by the ratio between its opening and
its focal length; the objective that utilises the larger back lens (or opening)
relatively to its focal length having necessarily the larger aperture. It would
hardly, therefore, serve any useful purpose if we were here to discuss the
various erroneous ideas that gave rise to the contention that 180° in air must
be the maximum aperture. Amongst these was the suggestion that the larger
emergent beams of immersion objectives were due to the fact that the
immersion fluid abolished the refractive action of the first plane surface
which, in the case of air, prevented there being any pencil exceeding 82°
within the glass. Also the very curious mistake which arose from the
the oil immersion, their relative apertures are immediately recognised, and
it is seen, for instance, that the aperture of the water immersion is somewhat
less than that of a dry objective of 180°, and that the aperture of the oil
immersion exceeds that of the latter by 30%.
The advantage of immersion, in comparison with dry objectives, becomes
at once apparent. Instead of consisting merely in a diminution of the loss of
light by reflection or increased working distance, it is seen that a wide-
angled immersion objective has a larger aperture than a dry objective of
maximum angle, so that for any of the purposes for which aperture is
essential an immersion must necessarily be preferred to a dry objective.
That pencils of identical angular extension but in different media are
different physically, will cease to appear in any way paradoxical if we recall
the simple optical fact that rays, which in air are spread out over the whole
hemisphere, are in a medium of higher refractive index such as oil
compressed into a cone of 82° round the perpendicular, i.e., twice the
critical angle. A cone exceeding twice the critical angle of the medium will
therefore embrace a surplus of rays which do not exist even in the
hemisphere when the object is in air.
The whole aperture question, notwithstanding the innumerable perplexities
which heretofore surrounded it, is in reality completely solved by these two
simple considerations: First, that “aperture” is to be applied in its ordinary
meaning as representing the greater or less capacity of the objective for
receiving and transmitting rays; and second, that when so applied the
aperture of an objective is determined by the ratio between its opening and
its focal length; the objective that utilises the larger back lens (or opening)
relatively to its focal length having necessarily the larger aperture. It would
hardly, therefore, serve any useful purpose if we were here to discuss the
various erroneous ideas that gave rise to the contention that 180° in air must
be the maximum aperture. Amongst these was the suggestion that the larger
emergent beams of immersion objectives were due to the fact that the
immersion fluid abolished the refractive action of the first plane surface
which, in the case of air, prevented there being any pencil exceeding 82°
within the glass. Also the very curious mistake which arose from the
Page 89
assumption that a hemisphere did not magnify an object at its centre
because the rays passed through without refraction. A further erroneous
view has, however, been so widespread that it seems to be desirable to
devote a few lines to it, especially as it always appears at first sight to be
both simple and conclusive.
If a dry objective is used upon an
object in air, as in Fig. 37, the angle
Fig. 37. may approach 180°, but when the
object is mounted in balsam, as in
Fig. 37a, the angle at the object
cannot exceed 82°, all rays outside
that limit (shown by dotted lines)
Fig. 37a.
being reflected back at the cover-
glass and not emerging into air. On
using an immersion objective, however, the immersion fluid which replaces
the air above the cover-glass allows the rays formerly reflected back to pass
through to the objective, so that the angle at the object may again be nearly
180° as with the dry lens. The action of the immersion objective was,
therefore, supposed to be simply that it repaired the loss in angle which was
occasioned when the object was transferred from air to balsam, and merely
restored the conditions existing in Fig. 37a with the dry objective on a dry
object.
As the result of this erroneous supposition, it followed that an immersion
objective could have no advantage over a dry objective, except in the case
of the latter being used upon a balsam-mounted object, its aperture then
being (as was supposed) “cut down.” The error lies simply in overlooking
the fact that the rays which are reflected back when the object is mounted in
balsam Fig. 37a) are not rays which are found when the object is in air (Fig.
37), but are additional and different rays which do not exist in air, as they
cannot be emitted in a substance of so low a refractive index.
Lastly, it should also be noted that it is numerical and not angular aperture
which measures the quantity of light admitted to the objective by different
pencils.
because the rays passed through without refraction. A further erroneous
view has, however, been so widespread that it seems to be desirable to
devote a few lines to it, especially as it always appears at first sight to be
both simple and conclusive.
If a dry objective is used upon an
object in air, as in Fig. 37, the angle
Fig. 37. may approach 180°, but when the
object is mounted in balsam, as in
Fig. 37a, the angle at the object
cannot exceed 82°, all rays outside
that limit (shown by dotted lines)
Fig. 37a.
being reflected back at the cover-
glass and not emerging into air. On
using an immersion objective, however, the immersion fluid which replaces
the air above the cover-glass allows the rays formerly reflected back to pass
through to the objective, so that the angle at the object may again be nearly
180° as with the dry lens. The action of the immersion objective was,
therefore, supposed to be simply that it repaired the loss in angle which was
occasioned when the object was transferred from air to balsam, and merely
restored the conditions existing in Fig. 37a with the dry objective on a dry
object.
As the result of this erroneous supposition, it followed that an immersion
objective could have no advantage over a dry objective, except in the case
of the latter being used upon a balsam-mounted object, its aperture then
being (as was supposed) “cut down.” The error lies simply in overlooking
the fact that the rays which are reflected back when the object is mounted in
balsam Fig. 37a) are not rays which are found when the object is in air (Fig.
37), but are additional and different rays which do not exist in air, as they
cannot be emitted in a substance of so low a refractive index.
Lastly, it should also be noted that it is numerical and not angular aperture
which measures the quantity of light admitted to the objective by different
pencils.
Page 90
Fig. 38. Fig. 38a.
First take the case of the medium being the same. The popular notion of a
pencil of light may be illustrated by Fig. 38, which assumes that there is
equal intensity of emission in all directions, so that the quantity of light
contained in any given pencils may be compared by simply comparing the
contents of the solid cones. The Bouguer-Lambert law, however, shows that
the quantity of light emitted by any bright point varies with the obliquity of
the direction of emission, being greater in a perpendicular than in an
oblique direction. The rays are less intense in proportion as they are more
inclined to the surface which emits them, so that a pencil is not correctly
represented by Fig. 38, but by Fig. 38a, the density of the rays decreasing
continuously from the vertical to the horizontal, and the squares of the sines
of the semi-angles (i.e., of the numerical aperture) constituting the true
measure of the quantity of light contained in any solid pencil.
If, again, the media are of different refractive indices, as air (1·0), water
(1·33), and oil (1·52), the total amount of light emitted over the whole 180°
from radiant points in these media under a given illumination is not the
same, but is greater in the case of the media of greater refractive indices in
the ratio of the squares of those indices (i.e., as 1·0, 1·77 and 2·25). The
quantity of light in pencils of different angle and in different media must
therefore be compared by squaring the product of the sines and the
refractive indices, i.e. (n Sin u2), for the square of the numerical aperture.
The fact is therefore made clear that the aperture of a dry objective of 180°
does not represent, as was supposed, a maximum, but that aperture
increases with the increase in the refractive index of the immersion fluid;
and it should be borne in mind that this result has been arrived at in strict
First take the case of the medium being the same. The popular notion of a
pencil of light may be illustrated by Fig. 38, which assumes that there is
equal intensity of emission in all directions, so that the quantity of light
contained in any given pencils may be compared by simply comparing the
contents of the solid cones. The Bouguer-Lambert law, however, shows that
the quantity of light emitted by any bright point varies with the obliquity of
the direction of emission, being greater in a perpendicular than in an
oblique direction. The rays are less intense in proportion as they are more
inclined to the surface which emits them, so that a pencil is not correctly
represented by Fig. 38, but by Fig. 38a, the density of the rays decreasing
continuously from the vertical to the horizontal, and the squares of the sines
of the semi-angles (i.e., of the numerical aperture) constituting the true
measure of the quantity of light contained in any solid pencil.
If, again, the media are of different refractive indices, as air (1·0), water
(1·33), and oil (1·52), the total amount of light emitted over the whole 180°
from radiant points in these media under a given illumination is not the
same, but is greater in the case of the media of greater refractive indices in
the ratio of the squares of those indices (i.e., as 1·0, 1·77 and 2·25). The
quantity of light in pencils of different angle and in different media must
therefore be compared by squaring the product of the sines and the
refractive indices, i.e. (n Sin u2), for the square of the numerical aperture.
The fact is therefore made clear that the aperture of a dry objective of 180°
does not represent, as was supposed, a maximum, but that aperture
increases with the increase in the refractive index of the immersion fluid;
and it should be borne in mind that this result has been arrived at in strict
Page 91
accordance with the ordinary propositions of geometrical optics, and
without any reference to or deductions from the diffraction theory of
Professor Abbe.
There still remains one other point for determination, namely, the proper
function of aperture in respect to immersion objectives of large aperture.
The explanation of the increased power of vision obtained by increase of
aperture was, that by the greater obliquity of the rays to the object “shadow
effects” were produced, a view which overlooked the fact, first, that the
utilisation of increased aperture depends not only on the obliquity of the
rays sent to the object, but also to the axis of the microscope; and exactly as
there is no acoustic shadow produced by an obstacle, which is only a few
multiples of the length of the sound waves, so there can be no shadow
produced by minute objects, only a few multiples from the light waves, the
latter then passing completely round the object. The Abbe diffraction
theory, however, supplies the true explanation of this, and shows that the
increased performance of immersion objectives of large aperture is directly
connected (as might have been anticipated) with the larger “openings” in
the proper sense of the term, which, as we have already explained, such
objectives really possess. Furthermore, in order that the image exactly
corresponds with the object, all diffracted rays must be gathered up by the
objective. Should any be lost we shall have not an actual image of the
object, but a spurious one. Now, if we have a coarse object, the diffracted
rays are all comprised within a narrow cone round the direct beam, and an
objective of small aperture will transmit them all. With a minute object,
however, the diffracted rays are widely spread out, so that a small aperture
can admit only a fractional part—to admit the whole or a very large part,
and consequently to see the minute structure of the object, or to see it truly,
a large aperture is necessary, and in this lies the value of aperture and of a
wide-angled immersion objective for the observation of minute structures.
Numerical Aperture.
Measure of Apertures of Objectives. N.A.—Numerical aperture, as it is
termed, is measured by the scale of measurement calculated by the late
Professor Abbe, and which has since been generally recognised and
without any reference to or deductions from the diffraction theory of
Professor Abbe.
There still remains one other point for determination, namely, the proper
function of aperture in respect to immersion objectives of large aperture.
The explanation of the increased power of vision obtained by increase of
aperture was, that by the greater obliquity of the rays to the object “shadow
effects” were produced, a view which overlooked the fact, first, that the
utilisation of increased aperture depends not only on the obliquity of the
rays sent to the object, but also to the axis of the microscope; and exactly as
there is no acoustic shadow produced by an obstacle, which is only a few
multiples of the length of the sound waves, so there can be no shadow
produced by minute objects, only a few multiples from the light waves, the
latter then passing completely round the object. The Abbe diffraction
theory, however, supplies the true explanation of this, and shows that the
increased performance of immersion objectives of large aperture is directly
connected (as might have been anticipated) with the larger “openings” in
the proper sense of the term, which, as we have already explained, such
objectives really possess. Furthermore, in order that the image exactly
corresponds with the object, all diffracted rays must be gathered up by the
objective. Should any be lost we shall have not an actual image of the
object, but a spurious one. Now, if we have a coarse object, the diffracted
rays are all comprised within a narrow cone round the direct beam, and an
objective of small aperture will transmit them all. With a minute object,
however, the diffracted rays are widely spread out, so that a small aperture
can admit only a fractional part—to admit the whole or a very large part,
and consequently to see the minute structure of the object, or to see it truly,
a large aperture is necessary, and in this lies the value of aperture and of a
wide-angled immersion objective for the observation of minute structures.
Numerical Aperture.
Measure of Apertures of Objectives. N.A.—Numerical aperture, as it is
termed, is measured by the scale of measurement calculated by the late
Professor Abbe, and which has since been generally recognised and
Page 92
adopted. He showed that even in lenses made for the same medium (as air)
their comparative aperture as compared with their focus was not correctly
measured by the angle of the rays grasped, but by the actual diameters of
the pencil of rays transmitted, which depend, as already seen, more upon
the back of the lens than the front. To get a geometric measure for
comparison, he took the radii, or half diameters (whose relative proportions
would be the same), and which geometrically are the sines of the semi-
angle of the outermost rays grasped. Abbe further showed that if this sine of
half the outside angle were multiplied by the refractive index of the medium
used we should have a number which would give the comparative aperture
of any lens, whatever the medium. This number, then, determines both the
numerical aperture and the resolving power of the objective.
The following table of numerical apertures shows the respective angular
pencils which they express in air, water and cedar oil, or glass.16 The first
column gives the numerical apertures from 0·20 to 1·33; the second, third,
and fourth, the air, water and oil (or balsam) angles of aperture from 23° 4′
air angle to 180° balsam angle. The theoretical resolving power in lines to
the inch is shown in the sixth column; the line E of the spectrum being
taken from about the middle of the green, the column giving “illuminating
power” being of less importance; while in using that of penetrating power, it
must be remembered that several data beside that of 1/a go to make up the
total depth of vision with the microscope.
ABRIDGED NUMERICAL APERTURE TABLE.
Limit of Resolving
Corresponding Angle Power,
(2 u) for in Lines to an Inch.
(1) (2) (3) (4) (5) (6) (7) (8) (9)
180° 122°
1·33 ... 128,225 138,989 168,907 1·769 ·752
0′ 6′
165° 120°
1·32 ... 127,261 137,944 167,637 1·742 ·758
56′ 33′
155° 117°
1·30 ... 125,333 135,854 165,097 1·690 ·769
38′ 35′
their comparative aperture as compared with their focus was not correctly
measured by the angle of the rays grasped, but by the actual diameters of
the pencil of rays transmitted, which depend, as already seen, more upon
the back of the lens than the front. To get a geometric measure for
comparison, he took the radii, or half diameters (whose relative proportions
would be the same), and which geometrically are the sines of the semi-
angle of the outermost rays grasped. Abbe further showed that if this sine of
half the outside angle were multiplied by the refractive index of the medium
used we should have a number which would give the comparative aperture
of any lens, whatever the medium. This number, then, determines both the
numerical aperture and the resolving power of the objective.
The following table of numerical apertures shows the respective angular
pencils which they express in air, water and cedar oil, or glass.16 The first
column gives the numerical apertures from 0·20 to 1·33; the second, third,
and fourth, the air, water and oil (or balsam) angles of aperture from 23° 4′
air angle to 180° balsam angle. The theoretical resolving power in lines to
the inch is shown in the sixth column; the line E of the spectrum being
taken from about the middle of the green, the column giving “illuminating
power” being of less importance; while in using that of penetrating power, it
must be remembered that several data beside that of 1/a go to make up the
total depth of vision with the microscope.
ABRIDGED NUMERICAL APERTURE TABLE.
Limit of Resolving
Corresponding Angle Power,
(2 u) for in Lines to an Inch.
(1) (2) (3) (4) (5) (6) (7) (8) (9)
180° 122°
1·33 ... 128,225 138,989 168,907 1·769 ·752
0′ 6′
165° 120°
1·32 ... 127,261 137,944 167,637 1·742 ·758
56′ 33′
155° 117°
1·30 ... 125,333 135,854 165,097 1·690 ·769
38′ 35′
Page 93
148° 114°
1·28 ... 123,405 133,764 162,557 1·638 ·781
42′ 44′
142° 111°
1·26 ... 121,477 131,674 160,017 1·588 ·794
39′ 59′
137° 109°
1·24 ... 119,548 129,584 157,477 1·538 ·806
36′ 20′
133° 106°
1·22 ... 117,620 127,494 154,937 1·488 ·820
4′ 45′
128° 104°
1·20 ... 115,692 125,404 152,397 1·440 ·833
55′ 15′
125° 101°
1·18 ... 113,764 123,314 149,857 1·392 ·847
3′ 50′
121°
1·16 ... 99° 29′ 111,835 121,224 147,317 1·346 ·862
26′
118°
1·14 ... 97° 11′ 109,907 119,134 144,777 1·300 ·877
0′
114°
1·12 ... 94° 55′ 107,979 117,044 142,237 1·254 ·893
44′
111°
1·10 ... 92° 43′ 106,051 114,954 139,698 1·210 ·909
36′
108°
1·08 ... 90° 34′ 104,123 112,864 137,158 1·166 ·926
36′
105°
1·06 ... 88° 27′ 102,195 110,774 134,618 1·124 ·943
42′
102°
1·04 ... 86° 21′ 100,266 108,684 132,078 1·082 ·962
53′
100°
1·02 ... 84° 18′ 98,338 106,593 129,538 1·040 ·980
10′
180°
1·00 97° 31′ 82° 17′ 96,410 104,503 126,998 1·000 1·000
0′
157°
0·98 94° 56′ 80° 17′ 94,482 102,413 124,458 ·960 1·020
2′
147°
0·96 92° 24′ 78° 20′ 92,554 100,323 121,918 ·922 1·042
29′
140°
0·94 89° 56′ 76° 24′ 90,625 98,223 119,378 ·884 1·064
6′
1·28 ... 123,405 133,764 162,557 1·638 ·781
42′ 44′
142° 111°
1·26 ... 121,477 131,674 160,017 1·588 ·794
39′ 59′
137° 109°
1·24 ... 119,548 129,584 157,477 1·538 ·806
36′ 20′
133° 106°
1·22 ... 117,620 127,494 154,937 1·488 ·820
4′ 45′
128° 104°
1·20 ... 115,692 125,404 152,397 1·440 ·833
55′ 15′
125° 101°
1·18 ... 113,764 123,314 149,857 1·392 ·847
3′ 50′
121°
1·16 ... 99° 29′ 111,835 121,224 147,317 1·346 ·862
26′
118°
1·14 ... 97° 11′ 109,907 119,134 144,777 1·300 ·877
0′
114°
1·12 ... 94° 55′ 107,979 117,044 142,237 1·254 ·893
44′
111°
1·10 ... 92° 43′ 106,051 114,954 139,698 1·210 ·909
36′
108°
1·08 ... 90° 34′ 104,123 112,864 137,158 1·166 ·926
36′
105°
1·06 ... 88° 27′ 102,195 110,774 134,618 1·124 ·943
42′
102°
1·04 ... 86° 21′ 100,266 108,684 132,078 1·082 ·962
53′
100°
1·02 ... 84° 18′ 98,338 106,593 129,538 1·040 ·980
10′
180°
1·00 97° 31′ 82° 17′ 96,410 104,503 126,998 1·000 1·000
0′
157°
0·98 94° 56′ 80° 17′ 94,482 102,413 124,458 ·960 1·020
2′
147°
0·96 92° 24′ 78° 20′ 92,554 100,323 121,918 ·922 1·042
29′
140°
0·94 89° 56′ 76° 24′ 90,625 98,223 119,378 ·884 1·064
6′
Page 94
133°
0·92 87° 32′ 74° 30′ 88,697 96,143 116,838 ·846 1·087
51′
128°
0·90 85° 10′ 72° 36′ 86,769 94,053 114,298 ·810 1·111
19′
123°
0·88 82° 51′ 70° 44′ 84,841 91,963 111,758 ·774 1·136
17′
118°
0·86 80° 34′ 68° 54′ 82,913 89,873 109,218 ·740 1·163
38′
114°
0·84 78° 20′ 67° 6′ 80,984 87,783 106,678 ·706 1·190
17′
110°
0·82 76° 8′ 65° 18′ 79,056 85,693 104,138 ·672 1·220
10′
106°
0·80 73° 58′ 63° 31′ 77,128 83,603 101,598 ·640 1·250
16′
102°
0·78 71° 49′ 61° 45′ 75,200 81,513 99,058 ·608 1·282
31′
0·76 98° 56′ 69° 42′ 60° 0′ 73,272 79,423 96,518 ·578 1·316
0·74 95° 28′ 67° 37′ 58° 16′ 71,343 77,333 93,979 ·548 1·351
0·72 92° 6′ 65° 32′ 56° 32′ 69,415 75,242 91,439 ·518 1·389
0·70 88° 51′ 63° 31′ 54° 50′ 67,487 73,152 88,899 ·490 1·429
0·68 85° 41′ 61° 30′ 53° 9′ 65,559 71,062 86,359 ·462 1·471
0·66 82° 36′ 59° 30′ 51° 28′ 63,631 68,972 83,819 ·436 1·515
0·64 79° 36′ 57° 31′ 49° 48′ 61,702 66,882 81,279 ·410 1·562
0·62 76° 38′ 55° 34′ 48° 9′ 59,774 64,792 78,739 ·384 1·613
0·60 73° 44′ 53° 38′ 46° 30′ 57,846 62,702 76,199 ·360 1·667
0·58 70° 54′ 51° 42′ 44° 51′ 55,918 60,612 73,659 ·336 1·724
0·56 68° 6′ 49° 48′ 43° 14′ 53,990 58,522 71,119 ·314 1·786
0·54 65° 22′ 47° 54′ 41° 37′ 52,061 56,432 68,579 ·292 1·852
0·52 62° 40′ 46° 2′ 40° 0′ 50,133 54,342 66,039 ·270 1·923
0·50 60° 0′ 44° 10′ 38° 24′ 48,205 52,252 63,499 ·250 2·000
0·45 53° 30′ 39° 33′ 34° 27′ 43,385 47,026 57,149 ·203 2·222
0·40 47° 9′ 35° 0′ 30° 31′ 38,564 41,801 50,799 ·160 2·500
0·35 40° 58′ 30° 30′ 26° 38′ 33,744 36,576 44,449 ·123 2·857
0·30 34° 56′ 26° 4′ 22° 46′ 28,923 31,351 38,099 ·090 3·333
0·25 28° 58′ 21° 40′ 18° 56′ 24,103 26,126 31,749 ·063 4·000
0·20 23° 4′ 17° 18′ 15° 7′ 19,282 20,901 25,400 ·040 5·000
0·92 87° 32′ 74° 30′ 88,697 96,143 116,838 ·846 1·087
51′
128°
0·90 85° 10′ 72° 36′ 86,769 94,053 114,298 ·810 1·111
19′
123°
0·88 82° 51′ 70° 44′ 84,841 91,963 111,758 ·774 1·136
17′
118°
0·86 80° 34′ 68° 54′ 82,913 89,873 109,218 ·740 1·163
38′
114°
0·84 78° 20′ 67° 6′ 80,984 87,783 106,678 ·706 1·190
17′
110°
0·82 76° 8′ 65° 18′ 79,056 85,693 104,138 ·672 1·220
10′
106°
0·80 73° 58′ 63° 31′ 77,128 83,603 101,598 ·640 1·250
16′
102°
0·78 71° 49′ 61° 45′ 75,200 81,513 99,058 ·608 1·282
31′
0·76 98° 56′ 69° 42′ 60° 0′ 73,272 79,423 96,518 ·578 1·316
0·74 95° 28′ 67° 37′ 58° 16′ 71,343 77,333 93,979 ·548 1·351
0·72 92° 6′ 65° 32′ 56° 32′ 69,415 75,242 91,439 ·518 1·389
0·70 88° 51′ 63° 31′ 54° 50′ 67,487 73,152 88,899 ·490 1·429
0·68 85° 41′ 61° 30′ 53° 9′ 65,559 71,062 86,359 ·462 1·471
0·66 82° 36′ 59° 30′ 51° 28′ 63,631 68,972 83,819 ·436 1·515
0·64 79° 36′ 57° 31′ 49° 48′ 61,702 66,882 81,279 ·410 1·562
0·62 76° 38′ 55° 34′ 48° 9′ 59,774 64,792 78,739 ·384 1·613
0·60 73° 44′ 53° 38′ 46° 30′ 57,846 62,702 76,199 ·360 1·667
0·58 70° 54′ 51° 42′ 44° 51′ 55,918 60,612 73,659 ·336 1·724
0·56 68° 6′ 49° 48′ 43° 14′ 53,990 58,522 71,119 ·314 1·786
0·54 65° 22′ 47° 54′ 41° 37′ 52,061 56,432 68,579 ·292 1·852
0·52 62° 40′ 46° 2′ 40° 0′ 50,133 54,342 66,039 ·270 1·923
0·50 60° 0′ 44° 10′ 38° 24′ 48,205 52,252 63,499 ·250 2·000
0·45 53° 30′ 39° 33′ 34° 27′ 43,385 47,026 57,149 ·203 2·222
0·40 47° 9′ 35° 0′ 30° 31′ 38,564 41,801 50,799 ·160 2·500
0·35 40° 58′ 30° 30′ 26° 38′ 33,744 36,576 44,449 ·123 2·857
0·30 34° 56′ 26° 4′ 22° 46′ 28,923 31,351 38,099 ·090 3·333
0·25 28° 58′ 21° 40′ 18° 56′ 24,103 26,126 31,749 ·063 4·000
0·20 23° 4′ 17° 18′ 15° 7′ 19,282 20,901 25,400 ·040 5·000
Page 95
INDEX:
(1) Numerical Aperture. (n sin u = a.)
(2) Air (n = 1·00).
(3) Water (n = 1·33).
(4) Homogeneous Immersion (n = 1·52).
(5) White Light. (λ = 0·5269 μ, Line E.)
(6) Monochromatic (Blue) Light.(λ = 0·4861 μ, Line F.)
(7) Photography. (λ = 0·4000 μ, Near Line hk.)
(8) Illuminating Power (a2.)
(9) Penetrating Power (1/a.)
Abbe’s Apertometer.
Fig. 39.—Abbe’s Apertometer.
The apertometer is an auxiliary piece of apparatus invented by Abbe, for
testing the fundamental properties of objectives and determining their
numerical and angular apertures. This accessory of the microscope involves
the same principles as that of Tolles, which the late Mr. J. Mayall and
myself brought to the notice of the Royal Microscopical Society of London
in 1876. Abbe’s apertometer (Fig. 39) consists of a flat cylinder of glass,
about three inches in diameter, and half an inch thick, with a large chord cut
off, so that the portion left is somewhat more than a semicircle; the part
where the segment is cut is bevelled from above downwards, to an angle of
(1) Numerical Aperture. (n sin u = a.)
(2) Air (n = 1·00).
(3) Water (n = 1·33).
(4) Homogeneous Immersion (n = 1·52).
(5) White Light. (λ = 0·5269 μ, Line E.)
(6) Monochromatic (Blue) Light.(λ = 0·4861 μ, Line F.)
(7) Photography. (λ = 0·4000 μ, Near Line hk.)
(8) Illuminating Power (a2.)
(9) Penetrating Power (1/a.)
Abbe’s Apertometer.
Fig. 39.—Abbe’s Apertometer.
The apertometer is an auxiliary piece of apparatus invented by Abbe, for
testing the fundamental properties of objectives and determining their
numerical and angular apertures. This accessory of the microscope involves
the same principles as that of Tolles, which the late Mr. J. Mayall and
myself brought to the notice of the Royal Microscopical Society of London
in 1876. Abbe’s apertometer (Fig. 39) consists of a flat cylinder of glass,
about three inches in diameter, and half an inch thick, with a large chord cut
off, so that the portion left is somewhat more than a semicircle; the part
where the segment is cut is bevelled from above downwards, to an angle of
Page 96
45°, and it will be seen that there is a small disc with an aperture in it
denoting the centre of the semicircle. To use this instrument the microscope
is placed in a vertical position, and the apertometer is placed upon the stage
with its circular part to the front and the chord to the back. Diffused light,
either from the sun or lamp, is assumed to be in front and on both sides.
Suppose the lens to be measured is a dry one-quarter inch; then with a one-
inch eye-piece having a large field, the centre disc, with its aperture on the
apertometer, is brought into focus. The eye-piece and the draw-tube are now
removed, leaving the focal arrangement undisturbed, and a lens supplied
with the apertometer is screwed into the end of the draw-tube. This lens,
with the eye-piece in the draw-tube, forms a low-power compound
microscope. This is now inserted into the body-tube, and the back lens of
the objective whose aperture we desire to measure is brought into focus. In
the image of the back lens will be seen stretched across, as it were, the
image of the circular part of the apertometer. It will appear as a bright band,
because the light which enters normally at the surface is reflected by the
bevelled part of the chord in a vertical direction, so that in reality a fan of
180° in air is formed. There are two sliding screens seen on either side of
the figure of the apertometer; they slide on the vertical circular portion of
the instrument. The images of these screens can be seen in the image of the
bright bands. These screens should now be moved so that their edges just
touch the periphery of the back lens. They act, as it were, as a diaphragm to
cut the fan and reduce it, so that its angle just equals the aperture of the
objective and no more.
This angle is now determined by the arc of glass between the screens; thus
we get an angle in glass the exact equivalent of the aperture of the
objective. As the numerical apertures of these arcs are engraved on the
apertometer, they can be read off by inspection. A difficulty is not
infrequently experienced from the fact that it is not easy to determine the
exact point at which the edge of the screen touches the periphery of the
back lens, or rather the limit of the aperture. Zeiss, to meet this difficulty,
made a change in the form of the apparatus—furnished a glass disc
mounted on a metal plate, with a slot for the purpose of its more accurate
adjustment.17
denoting the centre of the semicircle. To use this instrument the microscope
is placed in a vertical position, and the apertometer is placed upon the stage
with its circular part to the front and the chord to the back. Diffused light,
either from the sun or lamp, is assumed to be in front and on both sides.
Suppose the lens to be measured is a dry one-quarter inch; then with a one-
inch eye-piece having a large field, the centre disc, with its aperture on the
apertometer, is brought into focus. The eye-piece and the draw-tube are now
removed, leaving the focal arrangement undisturbed, and a lens supplied
with the apertometer is screwed into the end of the draw-tube. This lens,
with the eye-piece in the draw-tube, forms a low-power compound
microscope. This is now inserted into the body-tube, and the back lens of
the objective whose aperture we desire to measure is brought into focus. In
the image of the back lens will be seen stretched across, as it were, the
image of the circular part of the apertometer. It will appear as a bright band,
because the light which enters normally at the surface is reflected by the
bevelled part of the chord in a vertical direction, so that in reality a fan of
180° in air is formed. There are two sliding screens seen on either side of
the figure of the apertometer; they slide on the vertical circular portion of
the instrument. The images of these screens can be seen in the image of the
bright bands. These screens should now be moved so that their edges just
touch the periphery of the back lens. They act, as it were, as a diaphragm to
cut the fan and reduce it, so that its angle just equals the aperture of the
objective and no more.
This angle is now determined by the arc of glass between the screens; thus
we get an angle in glass the exact equivalent of the aperture of the
objective. As the numerical apertures of these arcs are engraved on the
apertometer, they can be read off by inspection. A difficulty is not
infrequently experienced from the fact that it is not easy to determine the
exact point at which the edge of the screen touches the periphery of the
back lens, or rather the limit of the aperture. Zeiss, to meet this difficulty,
made a change in the form of the apparatus—furnished a glass disc
mounted on a metal plate, with a slot for the purpose of its more accurate
adjustment.17
Page 97
Stereoscopic Binocular Vision.
Professor Wheatstone’s remarkable discovery of stereoscopic vision led, at
no distant period, to the application of the principle to the microscope. It
may therefore prove of interest to inquire how stereoscopic binocular vision
is brought about. Indeed, the curious results obtained in the stereoscope
cannot be well understood without a previous knowledge of the
fundamental optical principles involved in this contrivance, whereby two
slightly dissimilar pictures of any object become fused into one image,
having the actual appearance of relief. The invention of the stereoscope by
Sir Charles Wheatstone, F.R.S., 1838, and improved by Brewster, was
characterised by Sir John Herschel as “one of the most curious discoveries,
and beautiful for its simplicity, in the entire range of experimental optics,”
led to a more general appreciation of the value of the conjoint use of both
eyes in conveying to the mind impressions of the relative form and position
of an object, such as the use of either eye singly does not convey with
anything like the same precision. When a near object having three
dimensions is looked at, a different perspective representation is seen with
each eye. Certain parts are seen by the right eye, the left being closed, that
are invisible to the left eye, the right being closed, and the relative positions
of the portions visible to each eye in succession differ. These two visual
impressions are simultaneously perceived by both eyes, and combined in
the brain into one image, producing the effect of perspective and relief. If
truthful right-and-left monocular pictures of an object be so presented to the
two eyes that the optic axes when directed to them shall converge at the
same angle as when directed to the object itself, a solid image will be at
once perceived. The perception of relief referred to is closely connected
with the doubleness of vision which takes place when the images on
corresponding portions of the two retina are not similar. But, if in place of
looking at the solid object itself we look with the right and left eyes
respectively at pictures of the object corresponding to those which would be
formed by it on the retina of the two eyes if it were placed at a moderate
distance in front of them, and these visual pictures brought into
coincidence, the same conception of a solid form is generated in the mind
just as if the object itself were there.
Professor Wheatstone’s remarkable discovery of stereoscopic vision led, at
no distant period, to the application of the principle to the microscope. It
may therefore prove of interest to inquire how stereoscopic binocular vision
is brought about. Indeed, the curious results obtained in the stereoscope
cannot be well understood without a previous knowledge of the
fundamental optical principles involved in this contrivance, whereby two
slightly dissimilar pictures of any object become fused into one image,
having the actual appearance of relief. The invention of the stereoscope by
Sir Charles Wheatstone, F.R.S., 1838, and improved by Brewster, was
characterised by Sir John Herschel as “one of the most curious discoveries,
and beautiful for its simplicity, in the entire range of experimental optics,”
led to a more general appreciation of the value of the conjoint use of both
eyes in conveying to the mind impressions of the relative form and position
of an object, such as the use of either eye singly does not convey with
anything like the same precision. When a near object having three
dimensions is looked at, a different perspective representation is seen with
each eye. Certain parts are seen by the right eye, the left being closed, that
are invisible to the left eye, the right being closed, and the relative positions
of the portions visible to each eye in succession differ. These two visual
impressions are simultaneously perceived by both eyes, and combined in
the brain into one image, producing the effect of perspective and relief. If
truthful right-and-left monocular pictures of an object be so presented to the
two eyes that the optic axes when directed to them shall converge at the
same angle as when directed to the object itself, a solid image will be at
once perceived. The perception of relief referred to is closely connected
with the doubleness of vision which takes place when the images on
corresponding portions of the two retina are not similar. But, if in place of
looking at the solid object itself we look with the right and left eyes
respectively at pictures of the object corresponding to those which would be
formed by it on the retina of the two eyes if it were placed at a moderate
distance in front of them, and these visual pictures brought into
coincidence, the same conception of a solid form is generated in the mind
just as if the object itself were there.
Page 98
Professor Abbe, however, contended that the method by which dissimilar
images are formed in the binocular microscope differs materially from that
of ordinary stereoscopic vision, and that the pictures are united solely by the
activity of the brain, not by the prisms which ordinarily give rise to
sensations of solidity. This can be only partially true, as binocularity in the
microscope is due to difference of projection exhibited by the different
parallax displacement of the images, and also to the perception of depth
imparted by the instrument.
Wheatstone was firmly convinced that his stereoscopic principle could be
applied to the microscope, and he therefore applied first to Ross and then to
Powell to assist him in its adaptation. But whether either of these opticians
made any attempt to give effect to his wishes and suggestions is not known.
In the year 1851 Professor Riddell, of America, succeeded in constructing a
binocular microscope by employing two rectangular prisms behind the
objective. M. Nachet also constructed a binocular with two body-tubes and
a series of prisms. But neither Riddell’s nor Nachet’s instrument was ever
brought into use; they were either too complicated or too costly.
It will be understood, however, that the binocular stereoscope combines two
dissimilar pictures, while the binocular microscope simply enables the
observer to look with both eyes at images which are essentially identical.
Stereoscopic vision, to be effective, requires that the delineating pencil shall
be equally separated, so that one portion of the admitted cone of light is
conducted to one eye, and the other portion to the other eye.
Select any object lying in an inclined position, and place it in the centre of
the field of view of the microscope; then, with a card held close to the
object-glass, stop off alternately the right or left hand portion of the front
lens: it will then appear that during each alternate change certain parts of
the object will change their relative positions.
To illustrate this, Fig. 40 a, b are enlarged drawings of a portion of the egg
of the common bed-bug (Cimex lecticularis), the operculum which should
cover the opening having been forced off at the time the young was
hatched. The figures exactly represent the two positions that the inclined
orifice will occupy when the right- and left-hand portions of the object-
glass are stopped off. This object is viewed as an opaque object, and drawn
images are formed in the binocular microscope differs materially from that
of ordinary stereoscopic vision, and that the pictures are united solely by the
activity of the brain, not by the prisms which ordinarily give rise to
sensations of solidity. This can be only partially true, as binocularity in the
microscope is due to difference of projection exhibited by the different
parallax displacement of the images, and also to the perception of depth
imparted by the instrument.
Wheatstone was firmly convinced that his stereoscopic principle could be
applied to the microscope, and he therefore applied first to Ross and then to
Powell to assist him in its adaptation. But whether either of these opticians
made any attempt to give effect to his wishes and suggestions is not known.
In the year 1851 Professor Riddell, of America, succeeded in constructing a
binocular microscope by employing two rectangular prisms behind the
objective. M. Nachet also constructed a binocular with two body-tubes and
a series of prisms. But neither Riddell’s nor Nachet’s instrument was ever
brought into use; they were either too complicated or too costly.
It will be understood, however, that the binocular stereoscope combines two
dissimilar pictures, while the binocular microscope simply enables the
observer to look with both eyes at images which are essentially identical.
Stereoscopic vision, to be effective, requires that the delineating pencil shall
be equally separated, so that one portion of the admitted cone of light is
conducted to one eye, and the other portion to the other eye.
Select any object lying in an inclined position, and place it in the centre of
the field of view of the microscope; then, with a card held close to the
object-glass, stop off alternately the right or left hand portion of the front
lens: it will then appear that during each alternate change certain parts of
the object will change their relative positions.
To illustrate this, Fig. 40 a, b are enlarged drawings of a portion of the egg
of the common bed-bug (Cimex lecticularis), the operculum which should
cover the opening having been forced off at the time the young was
hatched. The figures exactly represent the two positions that the inclined
orifice will occupy when the right- and left-hand portions of the object-
glass are stopped off. This object is viewed as an opaque object, and drawn
Page 99
under a two-thirds object-glass of about
28° aperture. If this experiment is repeated,
by holding the card over the eye-piece, and
stopping off alternately the right and left
half of the ultimate emergent pencil,
exactly the same changes and appearances
will be observed in the object under view.
The two different images just produced are
such as are required for obtaining
stereoscopic vision. It is therefore evident
Fig. 40.—Portions of Eggs of Cimex. that if instead of bringing them confusedly
together into one eye we can separate them
so as to bring together a, b into the left and right eye, in the combined effect
of the two projections we obtain at once all that is necessary to enable us to
form a correct judgment of the solidity and distance of the several parts of
the object.
Nearly all objectives from the one inch upwards of any considerable
aperture give images of the object seen from a different point of view with
the two opposite extremes of the margin of the cone of rays; the resulting
effect is that there are a number of dissimilar perspectives of the object
blended together at one and the same time on the retina. For this reason, if
the object under view possesses bulk, a more accurate image will be
obtained by reducing the aperture of the objective.
28° aperture. If this experiment is repeated,
by holding the card over the eye-piece, and
stopping off alternately the right and left
half of the ultimate emergent pencil,
exactly the same changes and appearances
will be observed in the object under view.
The two different images just produced are
such as are required for obtaining
stereoscopic vision. It is therefore evident
Fig. 40.—Portions of Eggs of Cimex. that if instead of bringing them confusedly
together into one eye we can separate them
so as to bring together a, b into the left and right eye, in the combined effect
of the two projections we obtain at once all that is necessary to enable us to
form a correct judgment of the solidity and distance of the several parts of
the object.
Nearly all objectives from the one inch upwards of any considerable
aperture give images of the object seen from a different point of view with
the two opposite extremes of the margin of the cone of rays; the resulting
effect is that there are a number of dissimilar perspectives of the object
blended together at one and the same time on the retina. For this reason, if
the object under view possesses bulk, a more accurate image will be
obtained by reducing the aperture of the objective.
Page 100
Fig. 41.
Diagram 3, Fig. 41, represents the method employed by Mr. Wenham for
bringing the two eyes sufficiently close to each other to enable them both to
see through the double eye-piece at the same moment. a a a are rays
converging from the field lens of the eye-piece; after passing the eye-lens b,
if not intercepted, they would come to a focus at c; but they are arrested by
the inclined surfaces, d d, of two solid glass prisms. From the refraction of
the under incident surface of the prisms, the focus of the eye-piece becomes
elongated, and falls within the substance of the glass at e. The rays then
diverge, and after being reflected by the second inclined surface f, emerge
from the upper side of the prism, when their course is rendered still more
divergent, as shown by the figure. The reflecting angle given to the prisms
is 47½°, to accommodate which it is necessary to grind away the contact
edges of the prisms, as represented, otherwise they prevent the extreme
margins of the reflecting surfaces from coming into operation, which are
seldom made quite perfect.
Diagram 3, Fig. 41, represents the method employed by Mr. Wenham for
bringing the two eyes sufficiently close to each other to enable them both to
see through the double eye-piece at the same moment. a a a are rays
converging from the field lens of the eye-piece; after passing the eye-lens b,
if not intercepted, they would come to a focus at c; but they are arrested by
the inclined surfaces, d d, of two solid glass prisms. From the refraction of
the under incident surface of the prisms, the focus of the eye-piece becomes
elongated, and falls within the substance of the glass at e. The rays then
diverge, and after being reflected by the second inclined surface f, emerge
from the upper side of the prism, when their course is rendered still more
divergent, as shown by the figure. The reflecting angle given to the prisms
is 47½°, to accommodate which it is necessary to grind away the contact
edges of the prisms, as represented, otherwise they prevent the extreme
margins of the reflecting surfaces from coming into operation, which are
seldom made quite perfect.
Page 101
Fig. 42.—Professor Abbe’s Stereoscopic Eye-pieces.
Fig. 42 represents a sectional view of Abbe’s stereoscopic eye-pieces,
which consist of three prisms of crown glass, a, b and b′, placed below the
field-glass of the two eye-pieces; the tube c is slipped into the tube or body
like an ordinary eye-piece. The two prisms a and b are united so as to form
a thick plate with parallel sides, inclined to the axis at an angle of 38·5°.
The cone of rays from the objective is thus divided into two parts, one being
transmitted and the other reflected; that transmitted passing through a b and
forming an image of the object in the axial eye-piece B. Adjustment for
different distances between the eyes is effected by the screw placed to the
right-hand side of the figure, which moves the eye-piece B′, together with
the prism b′, in a parallel direction. The tubes can also be drawn out, if
greater separation is required. The special feature of this instrument is that
Fig. 42 represents a sectional view of Abbe’s stereoscopic eye-pieces,
which consist of three prisms of crown glass, a, b and b′, placed below the
field-glass of the two eye-pieces; the tube c is slipped into the tube or body
like an ordinary eye-piece. The two prisms a and b are united so as to form
a thick plate with parallel sides, inclined to the axis at an angle of 38·5°.
The cone of rays from the objective is thus divided into two parts, one being
transmitted and the other reflected; that transmitted passing through a b and
forming an image of the object in the axial eye-piece B. Adjustment for
different distances between the eyes is effected by the screw placed to the
right-hand side of the figure, which moves the eye-piece B′, together with
the prism b′, in a parallel direction. The tubes can also be drawn out, if
greater separation is required. The special feature of this instrument is that
Page 102
on halving the cone of rays by turning the caps, an orthoscopic or
pseudoscopic effect is produced. This double-eyed piece arrangement of
Abbe’s has not been at all brought into use in this country; this is partly
owing to its original adaptation for use with the shorter Continental body-
tube of 160 mm., and not for our 10-inch body.
The most perfect method of securing pleasing satisfactory stereoscopic
vision of objects is that devised by Mr. Wenham. In his binocular
microscope an equal division of the cone of rays, after passing through the
objective is secured and again united in the eye-pieces, which act as one, so
that each eye is furnished with an appropriate and simultaneous view of the
object. The methods contrived by the earlier experimenters not only
materially interfered with the definition of the objective and object, but also
required expensive alterations and adaptations of the microscope, and
sometimes separate stands for their employment. Mr. Wenham’s invention,
on the contrary, offers no such obstacle to its use, and the utility of the
microscope as a monocular is in no way impaired either when using the
higher powers.
The most important improvement, then,
effected by Wenham consists in the
splitting up or dividing the pencil of rays
proceeding from the objective by the
interposition of a prism of the form shown
in Fig. 43. This is placed in the body or
tube of the microscope so as to interrupt
only one-half (a c) of the pencil, the other
half (a b) proceeding continuously to the
field-glass, eye-piece, of the principal
body. The interrupted half of the pencil on
its entrance into the prism is subjected to
very slight refraction, since its axial ray is
perpendicular to the surface it meets.
Within, the prism is subjected to two Fig. 43.
reflections at b and c, which send it forth
again obliquely on the line b towards the eye-piece of the secondary body,
to the left-hand side of the figure; and since at its emergence its axial ray is
pseudoscopic effect is produced. This double-eyed piece arrangement of
Abbe’s has not been at all brought into use in this country; this is partly
owing to its original adaptation for use with the shorter Continental body-
tube of 160 mm., and not for our 10-inch body.
The most perfect method of securing pleasing satisfactory stereoscopic
vision of objects is that devised by Mr. Wenham. In his binocular
microscope an equal division of the cone of rays, after passing through the
objective is secured and again united in the eye-pieces, which act as one, so
that each eye is furnished with an appropriate and simultaneous view of the
object. The methods contrived by the earlier experimenters not only
materially interfered with the definition of the objective and object, but also
required expensive alterations and adaptations of the microscope, and
sometimes separate stands for their employment. Mr. Wenham’s invention,
on the contrary, offers no such obstacle to its use, and the utility of the
microscope as a monocular is in no way impaired either when using the
higher powers.
The most important improvement, then,
effected by Wenham consists in the
splitting up or dividing the pencil of rays
proceeding from the objective by the
interposition of a prism of the form shown
in Fig. 43. This is placed in the body or
tube of the microscope so as to interrupt
only one-half (a c) of the pencil, the other
half (a b) proceeding continuously to the
field-glass, eye-piece, of the principal
body. The interrupted half of the pencil on
its entrance into the prism is subjected to
very slight refraction, since its axial ray is
perpendicular to the surface it meets.
Within, the prism is subjected to two Fig. 43.
reflections at b and c, which send it forth
again obliquely on the line b towards the eye-piece of the secondary body,
to the left-hand side of the figure; and since at its emergence its axial ray is
Page 103
again perpendicular to the surface of the glass, it suffers no further
refraction on passing out of the prism than on entering. By this
arrangement, the image sent to the right eye is formed by rays which have
passed through the left half of the objective; whilst the image sent to the left
eye is formed by rays which have passed through the right half, and which
have been subjective to two reflections within the prism, and passing
through two surfaces of glass. The prism is held by the ends only on the
sides of a small brass drawer, so that all the four polished surfaces are
accessible, and should slide in so far that its edge may just reach the central
line of the objective, and be drawn back against a stop, so as to clear the
aperture of the same.
Fig. 44.—Sectional view of the Wenham Binocular.
refraction on passing out of the prism than on entering. By this
arrangement, the image sent to the right eye is formed by rays which have
passed through the left half of the objective; whilst the image sent to the left
eye is formed by rays which have passed through the right half, and which
have been subjective to two reflections within the prism, and passing
through two surfaces of glass. The prism is held by the ends only on the
sides of a small brass drawer, so that all the four polished surfaces are
accessible, and should slide in so far that its edge may just reach the central
line of the objective, and be drawn back against a stop, so as to clear the
aperture of the same.
Fig. 44.—Sectional view of the Wenham Binocular.
Page 104
The binocular, then (Fig. 44), consists of a small prism mounted in a brass
box A, which slides into an opening immediately above the object-glass,
and reflects one-half of the rays which form an image of the object, into an
additional tube B, attached at an inclination to the ordinary body C. One half
of the rays take the usual course with their performance unaltered; and the
remainder, though reflected twice, show no loss of light or definition
worthy of notice, if the prism be well made.
As the eyes of different persons are not the same distance apart, the first and
most important point to observe in using the binocular is that each eye has a
full and clear view of the object. This is easily tried by closing each eye
alternately without moving the head, when it may be found that some
adjustment is necessary by racking out the draw-tubes D, E, of the bodies by
means of the small milled head near the eye-pieces; this will increase the
distance of the centres; and, on the contrary, the tubes, when racked down,
will suit those eyes that are nearer together.
If the prism be drawn back till stopped by the small milled head, the field of
view in the inclined body is darkened, and the rays from the whole aperture
of the object-glass pass into the main body as usual, neither the prism nor
the additional body interfering in any way with the use of the instrument as
a monocular microscope.
The prism can be withdrawn altogether for the purpose of being wiped: this
should be done frequently, and very carefully, on all four surfaces, with a
perfectly clean cambric or silk handkerchief or a piece of wash-leather; but
no hard substance must be used. During this process the small piece of
blackened cork fitted between the prism and the thick end of the brass box
may be removed; but it must be carefully replaced in the same position, as it
serves an important purpose in stopping out extraneous light.
As the binocular microscope gives a real and natural appearance to objects,
this effect is considerably increased by employing those kinds of
illumination to which the naked eye is accustomed. The most suitable are
all the opaque methods where the light is thrown down upon the surface;
but for those objects that are semi-transparent, as sections of bone or teeth,
diatomaceæ, living aquatic animalcules, &c., the dark-field illumination by
means of the parabolic reflector will give an equally good result.
box A, which slides into an opening immediately above the object-glass,
and reflects one-half of the rays which form an image of the object, into an
additional tube B, attached at an inclination to the ordinary body C. One half
of the rays take the usual course with their performance unaltered; and the
remainder, though reflected twice, show no loss of light or definition
worthy of notice, if the prism be well made.
As the eyes of different persons are not the same distance apart, the first and
most important point to observe in using the binocular is that each eye has a
full and clear view of the object. This is easily tried by closing each eye
alternately without moving the head, when it may be found that some
adjustment is necessary by racking out the draw-tubes D, E, of the bodies by
means of the small milled head near the eye-pieces; this will increase the
distance of the centres; and, on the contrary, the tubes, when racked down,
will suit those eyes that are nearer together.
If the prism be drawn back till stopped by the small milled head, the field of
view in the inclined body is darkened, and the rays from the whole aperture
of the object-glass pass into the main body as usual, neither the prism nor
the additional body interfering in any way with the use of the instrument as
a monocular microscope.
The prism can be withdrawn altogether for the purpose of being wiped: this
should be done frequently, and very carefully, on all four surfaces, with a
perfectly clean cambric or silk handkerchief or a piece of wash-leather; but
no hard substance must be used. During this process the small piece of
blackened cork fitted between the prism and the thick end of the brass box
may be removed; but it must be carefully replaced in the same position, as it
serves an important purpose in stopping out extraneous light.
As the binocular microscope gives a real and natural appearance to objects,
this effect is considerably increased by employing those kinds of
illumination to which the naked eye is accustomed. The most suitable are
all the opaque methods where the light is thrown down upon the surface;
but for those objects that are semi-transparent, as sections of bone or teeth,
diatomaceæ, living aquatic animalcules, &c., the dark-field illumination by
means of the parabolic reflector will give an equally good result.
Page 105
For perfectly transparent illumination, it is much better to diffuse the light
by placing under the object various substances, such as tissue-paper, ground
glass, very thin porcelain, or a film of yellow bees’ wax, run between two
pieces of thin glass.
To ensure the full advantage and relief to both eyes in prolonged
observations with high as well as low powers, and with objectives of large
aperture, Mr. Wenham devised a compound prism for use with his binocular
microscope, the body tubes of which are also made expressly to suit the
prism, as extreme accuracy is necessary to bring them into proper position.
The main prism somewhat resembles in form the ordinary Wenham prism.
Over the first reflecting surface is placed a second smaller prism, the top
plane of which is parallel with the base of the first, so that direct rays pass
through without deviation, but at the two inclined surfaces of the prisms
(nearly in contact) there is a partial reflection from each, which, combined,
give as much light as in the direct tube. The reflected image from these two
surfaces is directed up into the inclined tube as usual. A somewhat later
improvement is that of Dr. Schroeder, the high power prism, by means of
which the whole of the rays emanating from the objective pass through it,
and the full aperture of any power is thereby effectively utilised.
Furthermore, Messrs. Ross have also constructed a right- and left-hand pair
of eye-pieces, which ensure greater perfection of the image. It was, in fact,
noticed that the size of the image in the left-hand field glass slightly
differed from that of the right when examined by the ordinary Huyghenian
eye-pieces. To compensate for this difference, the left-hand eye-piece has
been carefully calculated, and its focus is now so accurately adjusted that
the position of each eye in observing is brought into one plane of the
binocular. The pairs of the several series of eye-pieces A, B and C have also
been altered, and the effect is to greatly improve the image and give
increased comfort to the observer.
Dr. Carpenter, who warmly espoused the binocular, and constantly
employed it in his work, very truly said of it: “The important advantages I
find it to possess are in penetrating power, or focal depth, which is in every
way superior to that of the monocular microscope, so that an object whose
surface presents considerable inequalities is very much more distinctly seen
with the former than with the latter.”
by placing under the object various substances, such as tissue-paper, ground
glass, very thin porcelain, or a film of yellow bees’ wax, run between two
pieces of thin glass.
To ensure the full advantage and relief to both eyes in prolonged
observations with high as well as low powers, and with objectives of large
aperture, Mr. Wenham devised a compound prism for use with his binocular
microscope, the body tubes of which are also made expressly to suit the
prism, as extreme accuracy is necessary to bring them into proper position.
The main prism somewhat resembles in form the ordinary Wenham prism.
Over the first reflecting surface is placed a second smaller prism, the top
plane of which is parallel with the base of the first, so that direct rays pass
through without deviation, but at the two inclined surfaces of the prisms
(nearly in contact) there is a partial reflection from each, which, combined,
give as much light as in the direct tube. The reflected image from these two
surfaces is directed up into the inclined tube as usual. A somewhat later
improvement is that of Dr. Schroeder, the high power prism, by means of
which the whole of the rays emanating from the objective pass through it,
and the full aperture of any power is thereby effectively utilised.
Furthermore, Messrs. Ross have also constructed a right- and left-hand pair
of eye-pieces, which ensure greater perfection of the image. It was, in fact,
noticed that the size of the image in the left-hand field glass slightly
differed from that of the right when examined by the ordinary Huyghenian
eye-pieces. To compensate for this difference, the left-hand eye-piece has
been carefully calculated, and its focus is now so accurately adjusted that
the position of each eye in observing is brought into one plane of the
binocular. The pairs of the several series of eye-pieces A, B and C have also
been altered, and the effect is to greatly improve the image and give
increased comfort to the observer.
Dr. Carpenter, who warmly espoused the binocular, and constantly
employed it in his work, very truly said of it: “The important advantages I
find it to possess are in penetrating power, or focal depth, which is in every
way superior to that of the monocular microscope, so that an object whose
surface presents considerable inequalities is very much more distinctly seen
with the former than with the latter.”
Page 106
This difference may in part be attributed to the practical modification in the
angle of aperture of the objective, produced by the division of the cone of
rays transmitted through the two halves, so that the picture or image
received through each half of the objective of 60° is formed by rays
diverging at an angle of only about 30°. He confesses, however, that this
does not satisfactorily explain the fact that the binocular brings to the mind’s
eye the solid image of the object, and thus gives to the observer a good idea
of its form and which could hardly be obtained by the monocular
microscope. Carpenter cites in support of his views the wing of a little-
known moth, Zenzera Œsculi, which has an undulating surface, whereon
the scales are set at various angles instead of having the usual imbricated
arrangement, a good object for demonstrating; the general inequality of
surface and the obliquity of its scales, which are at once seen by the
binocular with a completeness not obtained by the monocular instrument.
To one unaccustomed to work with the binocular the views expressed by
Dr. Carpenter as to the extreme value of the instrument for ordinary work
may appear somewhat exaggerated, but from my own experience, having
long had in constant use a Ross-Zentmayer binocular, furnished with a
special prism, constructed for working with a 1⁄8 dry objective or a 1⁄10
immersion, the perfection of picture obtained was in every case quite equal
to that of the monocular microscope. The relief to the eyes can hardly be
over-estimated; the slight inequality of the pencil rays may be regarded
rather as a part of the welcome rest afforded when a prolonged examination
is made; it certainly appears to me to equalise the slight physiological
difference known to exist between the eyes of most people. If one image is
seen a little clearer by the stronger eye, the weaker eye assists rather more
the stereoscopic effect of the object under observation. The advantage
gained by the binocular is perhaps more appreciated when opaque objects
are under examination, as the eggs of insects, and the tongue of the blow-
fly, specimens of mosses, lichens, parasites (vegetable and animal), whose
planes and inequalities of surface require penetration, and which usually
demand more time for their observation.
angle of aperture of the objective, produced by the division of the cone of
rays transmitted through the two halves, so that the picture or image
received through each half of the objective of 60° is formed by rays
diverging at an angle of only about 30°. He confesses, however, that this
does not satisfactorily explain the fact that the binocular brings to the mind’s
eye the solid image of the object, and thus gives to the observer a good idea
of its form and which could hardly be obtained by the monocular
microscope. Carpenter cites in support of his views the wing of a little-
known moth, Zenzera Œsculi, which has an undulating surface, whereon
the scales are set at various angles instead of having the usual imbricated
arrangement, a good object for demonstrating; the general inequality of
surface and the obliquity of its scales, which are at once seen by the
binocular with a completeness not obtained by the monocular instrument.
To one unaccustomed to work with the binocular the views expressed by
Dr. Carpenter as to the extreme value of the instrument for ordinary work
may appear somewhat exaggerated, but from my own experience, having
long had in constant use a Ross-Zentmayer binocular, furnished with a
special prism, constructed for working with a 1⁄8 dry objective or a 1⁄10
immersion, the perfection of picture obtained was in every case quite equal
to that of the monocular microscope. The relief to the eyes can hardly be
over-estimated; the slight inequality of the pencil rays may be regarded
rather as a part of the welcome rest afforded when a prolonged examination
is made; it certainly appears to me to equalise the slight physiological
difference known to exist between the eyes of most people. If one image is
seen a little clearer by the stronger eye, the weaker eye assists rather more
the stereoscopic effect of the object under observation. The advantage
gained by the binocular is perhaps more appreciated when opaque objects
are under examination, as the eggs of insects, and the tongue of the blow-
fly, specimens of mosses, lichens, parasites (vegetable and animal), whose
planes and inequalities of surface require penetration, and which usually
demand more time for their observation.
Page 107
Fig. 45.—Swift-Stephenson’s Erecting Binocular.
No variation or change of any kind proposed either in the form of the
instrument or the prism has proved of sufficient value or importance to
bring it into use, and therefore Wenham’s instrument is scarcely likely to be
superseded. It must be admitted that the improvement effected in the eye-
piece form by Mr. Tolles, of Boston, U.S., is an exception to the rule laid
down. It consists in mounting the prisms in a light material, vulcanite, made
to fit into the monocular microscope body, thus taking the place of the
ordinary eye-piece. The image transmitted by the objective is brought to a
focus on the face of the first equilateral triangular prism by the intervention
of an erector-eye-piece inserted beneath it. The second set of prisms have a
rack and pinion movement to adjust them to any visual angle. The
illumination of both fields in this eye-piece is nearly equal in brightness.
No variation or change of any kind proposed either in the form of the
instrument or the prism has proved of sufficient value or importance to
bring it into use, and therefore Wenham’s instrument is scarcely likely to be
superseded. It must be admitted that the improvement effected in the eye-
piece form by Mr. Tolles, of Boston, U.S., is an exception to the rule laid
down. It consists in mounting the prisms in a light material, vulcanite, made
to fit into the monocular microscope body, thus taking the place of the
ordinary eye-piece. The image transmitted by the objective is brought to a
focus on the face of the first equilateral triangular prism by the intervention
of an erector-eye-piece inserted beneath it. The second set of prisms have a
rack and pinion movement to adjust them to any visual angle. The
illumination of both fields in this eye-piece is nearly equal in brightness.
Page 108
Mr. Stephenson’s erecting binocular (Fig. 45) has proved to be of some
practical value. It has the advantage of being of equal use with high and low
powers, and with little loss of definition. When used for dissecting purposes
it gives an erect image of the object. It is equally useful as a working
microscope, for arranging diatoms and botanical specimens of every kind.
The sub-stage tube will receive a diaphragm or illuminating apparatus; the
eye-pieces have a sliding adjustment for regulating the widths between
eyes.
Fig. 46.—An early form of the Ross-Wenham Binocular; nose-piece and prism-
holder detached.
practical value. It has the advantage of being of equal use with high and low
powers, and with little loss of definition. When used for dissecting purposes
it gives an erect image of the object. It is equally useful as a working
microscope, for arranging diatoms and botanical specimens of every kind.
The sub-stage tube will receive a diaphragm or illuminating apparatus; the
eye-pieces have a sliding adjustment for regulating the widths between
eyes.
Fig. 46.—An early form of the Ross-Wenham Binocular; nose-piece and prism-
holder detached.
Page 109
CHAPTER II.
Simple and Compound Microscope.
Microscopes are known as simple and compound. The simple microscope
may, for convenience, be divided into two classes; those used in the hand
(hand magnifiers), and those provided with a stand (mounted, as it is
termed) for supporting the object to be viewed, together with an adjustment
for the magnifying power, and a mirror for reflecting the light through the
object.
A simple microscope, mounted, is
preferable to a single lens, being
usually composed of two or more
lenses separated by a small distance
on a common axis; the increase of
the size of an object being the angle
it subtends to the eye of the observer,
or the angle formed by the
combination drawn from the axis of
vision to the extremity of the object,
as in Fig. 47. The lines drawn from
the eye to a and r form an angle,
Fig. 47.—Visual Angle. which, when the distance is small, is
nearly twice as large as the angle
from the eye to o w, formed by lines drawn at twice the distance. This is
called the angle of vision, or the visual angle. Now, the utility of a convex
lens interposed between a near object and the eye consists in its reducing
the divergence of the rays forming the several pencils issuing from it, so
that they enter the eye in a state of moderate divergence, as if they were
issuing from an object beyond the near point of distinct vision, and a well-
defined image is thereby formed upon the retina. In the next Fig. (48), a
Simple and Compound Microscope.
Microscopes are known as simple and compound. The simple microscope
may, for convenience, be divided into two classes; those used in the hand
(hand magnifiers), and those provided with a stand (mounted, as it is
termed) for supporting the object to be viewed, together with an adjustment
for the magnifying power, and a mirror for reflecting the light through the
object.
A simple microscope, mounted, is
preferable to a single lens, being
usually composed of two or more
lenses separated by a small distance
on a common axis; the increase of
the size of an object being the angle
it subtends to the eye of the observer,
or the angle formed by the
combination drawn from the axis of
vision to the extremity of the object,
as in Fig. 47. The lines drawn from
the eye to a and r form an angle,
Fig. 47.—Visual Angle. which, when the distance is small, is
nearly twice as large as the angle
from the eye to o w, formed by lines drawn at twice the distance. This is
called the angle of vision, or the visual angle. Now, the utility of a convex
lens interposed between a near object and the eye consists in its reducing
the divergence of the rays forming the several pencils issuing from it, so
that they enter the eye in a state of moderate divergence, as if they were
issuing from an object beyond the near point of distinct vision, and a well-
defined image is thereby formed upon the retina. In the next Fig. (48), a
Page 110
double-convex lens illustrates the action of the simple microscope, the small
arrow being the object brought under view, and the large arrow the
magnified image. The rays having first passed through the lens are bent into
nearly parallel lines, or pencils diverging from some point within the limits
of distinct vision. Thus altered, the eye receives rays precisely as if they had
emanated directly from a larger arrow placed about ten inches away from it.
The difference between the real and the imaginary object represents the
magnifying power of the lens. The object in this case is magnified nearly in
the proportion the focal distance of the lens bears to the distance of the
object when viewed by the unassisted eye; and this is due to the object
being more distinctly viewed so much nearer to the eye than it otherwise
could be without the lens.18
Fig. 48.—Virtual Image formed by Convex Lens.
It should be remembered that the shorter the focus and the nearer the eye
the magnifying lens is placed the smaller will be the diameter of the sphere
of which it forms a part, and unless its aperture be proportionally reduced,
the distinctness of the image will be destroyed by the spherical and
chromatic aberrations of its high curvature. Nevertheless, it was by the use
of lenses so constructed that the older microscopists—of whom
arrow being the object brought under view, and the large arrow the
magnified image. The rays having first passed through the lens are bent into
nearly parallel lines, or pencils diverging from some point within the limits
of distinct vision. Thus altered, the eye receives rays precisely as if they had
emanated directly from a larger arrow placed about ten inches away from it.
The difference between the real and the imaginary object represents the
magnifying power of the lens. The object in this case is magnified nearly in
the proportion the focal distance of the lens bears to the distance of the
object when viewed by the unassisted eye; and this is due to the object
being more distinctly viewed so much nearer to the eye than it otherwise
could be without the lens.18
Fig. 48.—Virtual Image formed by Convex Lens.
It should be remembered that the shorter the focus and the nearer the eye
the magnifying lens is placed the smaller will be the diameter of the sphere
of which it forms a part, and unless its aperture be proportionally reduced,
the distinctness of the image will be destroyed by the spherical and
chromatic aberrations of its high curvature. Nevertheless, it was by the use
of lenses so constructed that the older microscopists—of whom
Page 111
Leeuwenhoek was the more eminent—were enabled to do so much
excellent work.
The various kinds of simple pocket lenses for the most part consist of a
double-convex, or a plano-convex, or a combination of both, varying in
focal length from a quarter of an inch to two inches. Sometimes they are set
in pairs with a hole, a small diaphragm, cut in the piece of horn placed
between them. These are extremely useful for carrying in the waistcoat
pocket; to the anatomist and field botanist for examining various objects
and preparations.
Fig. 49.—Wollaston’s Doublet.
Perhaps the most important improvement effected in this form of the simple
microscope was that ascribed to the celebrated Dr. Wollaston, who devised
excellent work.
The various kinds of simple pocket lenses for the most part consist of a
double-convex, or a plano-convex, or a combination of both, varying in
focal length from a quarter of an inch to two inches. Sometimes they are set
in pairs with a hole, a small diaphragm, cut in the piece of horn placed
between them. These are extremely useful for carrying in the waistcoat
pocket; to the anatomist and field botanist for examining various objects
and preparations.
Fig. 49.—Wollaston’s Doublet.
Perhaps the most important improvement effected in this form of the simple
microscope was that ascribed to the celebrated Dr. Wollaston, who devised
Page 112
a doublet of two plano-convex lenses having their focal lengths, in the
proportion of one to three, mounted with their convex side directed towards
the eye of the observer, and the lens of shorter focal length next the object.
The explanation given of the correction thus effected in Dr. Wollaston’s
doublet will be best understood on reference to the annexed diagram, l l′, in
Fig. 49, being the object for a segment of the cornea of the eye, and d d′ the
stop or diaphragm. Now, it will be seen that each pencil of light proceeding
from l l′, the object, is rendered excentrical by the limiting aperture or the
diaphragm d d; consequently, they pass through the lenses on opposite sides
of their common axis o p; thus each becomes affected by opposite errors,
which to some extent balance and correct each other. To take the pencil l,
for instance, as it enters the eye at r b; r b is bent to the right at the first
lens, and to the left at the second; and as each bending alters the direction of
the blue ray more than the red, and as the blue ray falls nearer the margin of
the second lens, where the refraction is greater than that nearer the centre,
and compensates to some extent for the greater focal length of the second
lens, the blue rays will emerge very nearly parallel, and colourless to the
eye. At the same time, its spherical aberration has been diminished, since
the side of the pencil as it proceeds through one lens passes nearer the axis,
and in the other nearer the margin.
This must be taken to apply to pencils farthest from the centre of the object.
Central rays, it is obvious, would pass both lenses symmetrically, the same
portions of rays occupying nearly the same relative places in both lenses.
The blue ray would enter the second lens nearer its axis than the red; and
being thus less refracted than the red by the second lens, some amount of
compensation would take place, differing in principle, and inferior in
degree, to that which is found in the excentrical pencils. In the intermediate
spaces the corrections are still more imperfect and uncertain; and this
explains the cause of aberrations which must of necessity exist even in the
best-made doublet. It is, however, infinitely superior to a single lens, and
will transmit a pencil of an angle of from 35° to 50°.
The next step towards improving the simple microscope was in relation to
the eye-piece, and was effected by Holland. It consisted in substituting two
lenses for the first in the doublet, and placing a stop between them and the
third. The first bending of the pencils of light being effected by two lenses
proportion of one to three, mounted with their convex side directed towards
the eye of the observer, and the lens of shorter focal length next the object.
The explanation given of the correction thus effected in Dr. Wollaston’s
doublet will be best understood on reference to the annexed diagram, l l′, in
Fig. 49, being the object for a segment of the cornea of the eye, and d d′ the
stop or diaphragm. Now, it will be seen that each pencil of light proceeding
from l l′, the object, is rendered excentrical by the limiting aperture or the
diaphragm d d; consequently, they pass through the lenses on opposite sides
of their common axis o p; thus each becomes affected by opposite errors,
which to some extent balance and correct each other. To take the pencil l,
for instance, as it enters the eye at r b; r b is bent to the right at the first
lens, and to the left at the second; and as each bending alters the direction of
the blue ray more than the red, and as the blue ray falls nearer the margin of
the second lens, where the refraction is greater than that nearer the centre,
and compensates to some extent for the greater focal length of the second
lens, the blue rays will emerge very nearly parallel, and colourless to the
eye. At the same time, its spherical aberration has been diminished, since
the side of the pencil as it proceeds through one lens passes nearer the axis,
and in the other nearer the margin.
This must be taken to apply to pencils farthest from the centre of the object.
Central rays, it is obvious, would pass both lenses symmetrically, the same
portions of rays occupying nearly the same relative places in both lenses.
The blue ray would enter the second lens nearer its axis than the red; and
being thus less refracted than the red by the second lens, some amount of
compensation would take place, differing in principle, and inferior in
degree, to that which is found in the excentrical pencils. In the intermediate
spaces the corrections are still more imperfect and uncertain; and this
explains the cause of aberrations which must of necessity exist even in the
best-made doublet. It is, however, infinitely superior to a single lens, and
will transmit a pencil of an angle of from 35° to 50°.
The next step towards improving the simple microscope was in relation to
the eye-piece, and was effected by Holland. It consisted in substituting two
lenses for the first in the doublet, and placing a stop between them and the
third. The first bending of the pencils of light being effected by two lenses
Page 113
instead of one, produces less spherical and chromatic aberration, which are
more nearly balanced or corrected at the second bending, and in the
opposite direction, by the third lens.
Another form of simple lens was devised by Dr. Wollaston, the
“Periscopic.” This combination consists of two hemispherical lenses
cemented together by their plane faces, with a stop between them to limit
the aperture. A similar proposal, made by Sir David Brewster in 1820, is
known as the Coddington lens,19 shown at Fig. 50: this has a somewhat
larger field, and is equally balanced in all directions, as is made evident, the
pencils a b and b a passing through under precisely the same circumstances.
Its spherical form has the further advantage of rendering the position in
which it is held of comparatively little consequence. It is still used as a hand
magnifier, although its definition is certainly not so good as that of a well-
made doublet. It is usually set in a folding case, as represented in the figure,
and so contrived as to be admirably adapted for the waistcoat-pocket. It is
usually sold with the small holder, Fig. 50a, for holding and securing small
objects during examination. Browning’s Platyscopic Pocket Lens is a useful
form of pocket lens for the botanist and mineralogist. Its focus is nearly
three times longer than that of the Coddington, and allows of opaque
objects being more easily examined; it has also a magnifying power of 15,
20, and 30 diameters.
more nearly balanced or corrected at the second bending, and in the
opposite direction, by the third lens.
Another form of simple lens was devised by Dr. Wollaston, the
“Periscopic.” This combination consists of two hemispherical lenses
cemented together by their plane faces, with a stop between them to limit
the aperture. A similar proposal, made by Sir David Brewster in 1820, is
known as the Coddington lens,19 shown at Fig. 50: this has a somewhat
larger field, and is equally balanced in all directions, as is made evident, the
pencils a b and b a passing through under precisely the same circumstances.
Its spherical form has the further advantage of rendering the position in
which it is held of comparatively little consequence. It is still used as a hand
magnifier, although its definition is certainly not so good as that of a well-
made doublet. It is usually set in a folding case, as represented in the figure,
and so contrived as to be admirably adapted for the waistcoat-pocket. It is
usually sold with the small holder, Fig. 50a, for holding and securing small
objects during examination. Browning’s Platyscopic Pocket Lens is a useful
form of pocket lens for the botanist and mineralogist. Its focus is nearly
three times longer than that of the Coddington, and allows of opaque
objects being more easily examined; it has also a magnifying power of 15,
20, and 30 diameters.
Page 114
Fig. 50.—The Coddington Lens. Fig. 50a.
One of the best combinations of the hand or
pocket form of lens is that known as Steinheil’s
aplanatic lens (Fig. 51); it consists of a bi-
convex lens cemented between two concavo-
convex lenses, giving a relatively long focal
distance and a large flat field. The higher
powers of this lens are much used for
dissecting purposes. This handy magnifier Fig. 51.—Steinheil’s Aplanatic Lens.
appears to have suggested a later combination,
the apochromatic of Zeiss. No hand lens can compare with Steinheil’s
“loups.”
One of the best combinations of the hand or
pocket form of lens is that known as Steinheil’s
aplanatic lens (Fig. 51); it consists of a bi-
convex lens cemented between two concavo-
convex lenses, giving a relatively long focal
distance and a large flat field. The higher
powers of this lens are much used for
dissecting purposes. This handy magnifier Fig. 51.—Steinheil’s Aplanatic Lens.
appears to have suggested a later combination,
the apochromatic of Zeiss. No hand lens can compare with Steinheil’s
“loups.”
Page 115
Fig. 52.—Simple Microscope.
When the magnifying power of a lens is considerable, or when its focal
length is short, or it is wished to use it with greater precision and steadiness,
it should be mounted on a short stand with a tubular stem, with rack-work
focussing movement and mirror illumination. Fig. 52 represents a simple
dissecting microscope, with a glass circular stage, 4½ inches in diameter,
supported on three legs—a handy and useful form of instrument for many
purposes.
The Compound Microscope.
The compound microscope differs from the simple, inasmuch as the image
is formed by an object-glass, and further magnified by one or more lenses
forming an eye-glass. For a microscope to be a compound one, its essential
qualification is that it should have an object-glass or objective, and an eye-
glass or eye-piece, so called because they are respectively near the object
and the eye of the observer when the instrument is in use. The microscope
When the magnifying power of a lens is considerable, or when its focal
length is short, or it is wished to use it with greater precision and steadiness,
it should be mounted on a short stand with a tubular stem, with rack-work
focussing movement and mirror illumination. Fig. 52 represents a simple
dissecting microscope, with a glass circular stage, 4½ inches in diameter,
supported on three legs—a handy and useful form of instrument for many
purposes.
The Compound Microscope.
The compound microscope differs from the simple, inasmuch as the image
is formed by an object-glass, and further magnified by one or more lenses
forming an eye-glass. For a microscope to be a compound one, its essential
qualification is that it should have an object-glass or objective, and an eye-
glass or eye-piece, so called because they are respectively near the object
and the eye of the observer when the instrument is in use. The microscope
Page 116
consists of a tube or body, and a stand, an arrangement for carrying the
body, combined with which is a stage for holding the object, and a mirror
for its illumination. To the more modern instrument has been added a
substage, to carry a condenser and other accessories.
The body of a microscope, which carries the system of magnifying lenses,
must be placed at one particular distance from the object, termed the focus,
in order that a clear image may be obtained. For the purpose of focussing
two motions are supplied, the one for coarse adjustment, with lower
powers; the other for higher powers, termed the fine adjustment. It is in this
wise that the magnifying power of the compound microscope is turned to
good account.
There are, however, limits to the use to which lenses can be put with
advantage in the direction of magnifying the object, just as there are in
varying the magnifying power of the eye-glass. Defects in either, although
not first seen, that is, when the image is but moderately enlarged, are
brought into prominence by greater amplification. In practice, therefore, it
is found to be of advantage to vary the power by employing object-glasses
of different values (foci). In whatever way increase of amplification is
brought about, two things will always result from the change: the
proportion of surface of the object of which an image can be formed must
be diminished, and the amount of light spread over the image proportionally
lessened.
In addition to the two lenses mentioned, it was found to be of considerable
advantage to introduce a third lens between the object-glass and the image
formed by it at eye-piece, the purport of which is to change the course of
the rays (bend in the pencil) so that the image may not be found of too great
a dimension for the whole to be brought within the circumference of the
eye-glass. This, it will be readily seen, allows more of the object to be
viewed at the same time by the field-glass, as the eye-piece of the
microscope is termed.
Fig. 53 represents the body of an ordinary compound microscope with its
triplet object-glasses; o is an object, above it is the triple achromatic object-
glass, in connection with the eye-piece e e, f f the plano-convex lenses; e e
being the eye-glass, and f f the field-glass, between which, at b b, the arrow
body, combined with which is a stage for holding the object, and a mirror
for its illumination. To the more modern instrument has been added a
substage, to carry a condenser and other accessories.
The body of a microscope, which carries the system of magnifying lenses,
must be placed at one particular distance from the object, termed the focus,
in order that a clear image may be obtained. For the purpose of focussing
two motions are supplied, the one for coarse adjustment, with lower
powers; the other for higher powers, termed the fine adjustment. It is in this
wise that the magnifying power of the compound microscope is turned to
good account.
There are, however, limits to the use to which lenses can be put with
advantage in the direction of magnifying the object, just as there are in
varying the magnifying power of the eye-glass. Defects in either, although
not first seen, that is, when the image is but moderately enlarged, are
brought into prominence by greater amplification. In practice, therefore, it
is found to be of advantage to vary the power by employing object-glasses
of different values (foci). In whatever way increase of amplification is
brought about, two things will always result from the change: the
proportion of surface of the object of which an image can be formed must
be diminished, and the amount of light spread over the image proportionally
lessened.
In addition to the two lenses mentioned, it was found to be of considerable
advantage to introduce a third lens between the object-glass and the image
formed by it at eye-piece, the purport of which is to change the course of
the rays (bend in the pencil) so that the image may not be found of too great
a dimension for the whole to be brought within the circumference of the
eye-glass. This, it will be readily seen, allows more of the object to be
viewed at the same time by the field-glass, as the eye-piece of the
microscope is termed.
Fig. 53 represents the body of an ordinary compound microscope with its
triplet object-glasses; o is an object, above it is the triple achromatic object-
glass, in connection with the eye-piece e e, f f the plano-convex lenses; e e
being the eye-glass, and f f the field-glass, between which, at b b, the arrow
Page 117
represents the diaphragm. The course of the light is shown by
three rays drawn from the centre, and three from each end of
the object o; these rays, if not prevented by the lens f f, and
the diaphragm b b, would form an image at a a; but here, as
they meet with the lens f f in their passage, are converged by it
at b b, the diaphragm at b b intercepting a portion of
peripheral rays, permitting only those to pass that are
necessary for the formation of the image, the further
magnification of which is, however, here brought about by the
eye-glass e e, precisely as if it were that of the original object
under examination. It will be apparent, then, that the field-
lens f f belongs in principle to the object-glass, or objective,
taking a share in the image-forming rays, although this is
taken to be a part of the eye-piece.
Fig. 53.
Evolution of the Modern Achromatic Microscope.
The great advances made in the optical arrangements of the modern
microscope necessitated important changes and improvements in its several
mechanical parts. Indeed, as the apertures of objectives became increased,
and focal planes became correspondingly shallower, it was absolutely
necessary to apply a more sensitive system of focussing than that for many
years past commonly in use. The leading manufacturers at once grasped the
situation, and in a short space of time the older model microscopes were
discarded, and replaced by instruments better in workmanship and finish,
and in every way more suitable for the student and the promotion of
original scientific research.
From an early period English amateurs appear to have bestowed greater
attention on the improvement of the microscope than those of any other
country. Between 1820 and 1835 Tully, Pritchard, Dolland, James Smith,
Andrew Ross, and Hugh Powell, encouraged by Wollaston, Brewster,
Goring, Herschel, and Lister, worked out innumerable combinations of
three rays drawn from the centre, and three from each end of
the object o; these rays, if not prevented by the lens f f, and
the diaphragm b b, would form an image at a a; but here, as
they meet with the lens f f in their passage, are converged by it
at b b, the diaphragm at b b intercepting a portion of
peripheral rays, permitting only those to pass that are
necessary for the formation of the image, the further
magnification of which is, however, here brought about by the
eye-glass e e, precisely as if it were that of the original object
under examination. It will be apparent, then, that the field-
lens f f belongs in principle to the object-glass, or objective,
taking a share in the image-forming rays, although this is
taken to be a part of the eye-piece.
Fig. 53.
Evolution of the Modern Achromatic Microscope.
The great advances made in the optical arrangements of the modern
microscope necessitated important changes and improvements in its several
mechanical parts. Indeed, as the apertures of objectives became increased,
and focal planes became correspondingly shallower, it was absolutely
necessary to apply a more sensitive system of focussing than that for many
years past commonly in use. The leading manufacturers at once grasped the
situation, and in a short space of time the older model microscopes were
discarded, and replaced by instruments better in workmanship and finish,
and in every way more suitable for the student and the promotion of
original scientific research.
From an early period English amateurs appear to have bestowed greater
attention on the improvement of the microscope than those of any other
country. Between 1820 and 1835 Tully, Pritchard, Dolland, James Smith,
Andrew Ross, and Hugh Powell, encouraged by Wollaston, Brewster,
Goring, Herschel, and Lister, worked out innumerable combinations of
Page 118
single and compound lenses to be employed as simple microscopes,
explained in a previous chapter.
The theories propounded about this time for the improvement of lenses and
the various combinations for amateurs were not of lasting value.
Nevertheless, they were not wholly made in vain, as during the last twenty
years they have indirectly borne good fruit, inasmuch as by working in
another direction Professor Abbe was led to the discovery of new and better
kinds of glass, by which the secondary spectrum has been so nearly
eliminated, and the optical parts of the microscope so materially improved.
In pursuing this subject I would not have it supposed that Continental
opticians were either idle or supine. On the contrary, Oberhäuser,
Fraunhofer, Chevalier, Nachet, Hartnach, and others took an active part in
the work.
The compound microscope made for anatomists by the first-named optician
about 1825 has not been entirely superseded. He was the first to make a
rotating stage, to apply mechanism to focussing, and to introduce the
system of direct push or pull of the condenser tube within the sub-stage
socket. Nachet made other improvements on the Oberhäuser microscope by
applying under the stage a tail-piece having a dove-tailed groove in which a
slide carrying the sub-stage was moved by a stud-pin. More recently the
lever movement was superseded by American opticians, who made other
changes. Hartnach ultimately very much improved Oberhäuser’s model, and
this remains with us.
The English modern compound microscope, together with the achromatic
objective, we owe to a mind teeming with scientific inventions, Joseph
Jackson Lister, F.R.S., who in 1826 supplied Mr. Tully, a well-known
London optician of that period, with original drawings for the important
improvements in its mechanical details and accessory apparatus which
followed so soon afterwards.
Among the many ingenious novelties enumerated in his published papers
we find the graduated lengthening of the body-tube of the microscope; a
stage-fitting for clamping and rotating the object; a subsidiary stage; a dark-
well, and a large disc to incline and rotate opaque objects; a ground-glass
light moderator; a live-box with bevelled flat-glass plate; an erector-eye-
explained in a previous chapter.
The theories propounded about this time for the improvement of lenses and
the various combinations for amateurs were not of lasting value.
Nevertheless, they were not wholly made in vain, as during the last twenty
years they have indirectly borne good fruit, inasmuch as by working in
another direction Professor Abbe was led to the discovery of new and better
kinds of glass, by which the secondary spectrum has been so nearly
eliminated, and the optical parts of the microscope so materially improved.
In pursuing this subject I would not have it supposed that Continental
opticians were either idle or supine. On the contrary, Oberhäuser,
Fraunhofer, Chevalier, Nachet, Hartnach, and others took an active part in
the work.
The compound microscope made for anatomists by the first-named optician
about 1825 has not been entirely superseded. He was the first to make a
rotating stage, to apply mechanism to focussing, and to introduce the
system of direct push or pull of the condenser tube within the sub-stage
socket. Nachet made other improvements on the Oberhäuser microscope by
applying under the stage a tail-piece having a dove-tailed groove in which a
slide carrying the sub-stage was moved by a stud-pin. More recently the
lever movement was superseded by American opticians, who made other
changes. Hartnach ultimately very much improved Oberhäuser’s model, and
this remains with us.
The English modern compound microscope, together with the achromatic
objective, we owe to a mind teeming with scientific inventions, Joseph
Jackson Lister, F.R.S., who in 1826 supplied Mr. Tully, a well-known
London optician of that period, with original drawings for the important
improvements in its mechanical details and accessory apparatus which
followed so soon afterwards.
Among the many ingenious novelties enumerated in his published papers
we find the graduated lengthening of the body-tube of the microscope; a
stage-fitting for clamping and rotating the object; a subsidiary stage; a dark-
well, and a large disc to incline and rotate opaque objects; a ground-glass
light moderator; a live-box with bevelled flat-glass plate; an erector-eye-
Page 119
piece; an adapter for using Wollaston’s camera lucida for microscopical
drawing; and, above all, a combination of lenses to act as a condenser under
the object (evidently the first approach to the present achromatic sub-stage
condenser). The value of the erector-eye-piece for facilitating dissections
under the microscope is not even yet sufficiently appreciated. Tully
published a descriptive account of Lister’s microscope, the first one of
which he made, and acknowledged his indebtedness to “Mr. Lister’s
ingenuity and skill.” Shortly afterwards Lister made known his discovery of
the two aplanatic foci in a double achromatic object glass, and gave verbal
directions to the three principal makers of microscopes in London, James
Smith, Andrew Ross, and Hugh Powell, for the future construction of the
achromatic objective, all of whom were intent on the improvement of their
several models. To the latter the Society of Arts awarded, in 1832, a medal
for his improved mechanical stage movements, on the “Turrell system,”
which Powell first constructed for Edmund Turrell. This stage was made to
rotate completely on its optic axis by means of an obliquely-placed pinion
acting on a bevelled rack on the inner face of the stage-ring supporting the
mechanism. In 1834 Powell once more received a Society of Arts medal,
“the Iris,” for improvements in the application of a new form of fine
adjustment.
About the same date (1835) Andrew Ross introduced the socket-carrier of
the body-tube of the microscope on a strong stem, with rack bent in the
middle, thus affording space for a larger stage. He likewise devised the
hollow cross-bar, placed at right angles to the rack-stem, whereby he was
enabled to use a new system of fine adjustment, consisting of a delicate
screw with large milled head, acting by a point on the long arm of a lever,
the short arm of which ends in a fork in contact with a stud placed on either
side of a cylindrical sliding tube forming the nose-piece of the body-tube,
and into which the objective is screwed. A spiral spring presses down the
nose-piece, and against this the screw and lever act.
This appears to have been the first really sensitive focussing method applied
to the nose-piece; it was, and probably is, one of the most delicate systems
ever applied to the microscope. It has enjoyed a long period of popularity,
and I believe it still survives in Powell and Lealand’s instruments, which are
drawing; and, above all, a combination of lenses to act as a condenser under
the object (evidently the first approach to the present achromatic sub-stage
condenser). The value of the erector-eye-piece for facilitating dissections
under the microscope is not even yet sufficiently appreciated. Tully
published a descriptive account of Lister’s microscope, the first one of
which he made, and acknowledged his indebtedness to “Mr. Lister’s
ingenuity and skill.” Shortly afterwards Lister made known his discovery of
the two aplanatic foci in a double achromatic object glass, and gave verbal
directions to the three principal makers of microscopes in London, James
Smith, Andrew Ross, and Hugh Powell, for the future construction of the
achromatic objective, all of whom were intent on the improvement of their
several models. To the latter the Society of Arts awarded, in 1832, a medal
for his improved mechanical stage movements, on the “Turrell system,”
which Powell first constructed for Edmund Turrell. This stage was made to
rotate completely on its optic axis by means of an obliquely-placed pinion
acting on a bevelled rack on the inner face of the stage-ring supporting the
mechanism. In 1834 Powell once more received a Society of Arts medal,
“the Iris,” for improvements in the application of a new form of fine
adjustment.
About the same date (1835) Andrew Ross introduced the socket-carrier of
the body-tube of the microscope on a strong stem, with rack bent in the
middle, thus affording space for a larger stage. He likewise devised the
hollow cross-bar, placed at right angles to the rack-stem, whereby he was
enabled to use a new system of fine adjustment, consisting of a delicate
screw with large milled head, acting by a point on the long arm of a lever,
the short arm of which ends in a fork in contact with a stud placed on either
side of a cylindrical sliding tube forming the nose-piece of the body-tube,
and into which the objective is screwed. A spiral spring presses down the
nose-piece, and against this the screw and lever act.
This appears to have been the first really sensitive focussing method applied
to the nose-piece; it was, and probably is, one of the most delicate systems
ever applied to the microscope. It has enjoyed a long period of popularity,
and I believe it still survives in Powell and Lealand’s instruments, which are
Page 120
very generally admitted to be of superior excellence for all purposes where
extreme delicacy of focussing is an essential element.
The rival system of fine adjustment—the short lever and screw applied
externally to the body-tube—known as the Lister-Jackson system, which
appears to have been contrived to allow the body-tube to be supported more
firmly on the limb or stem, has had its merits ably realised in the
microscopes of Smith and Beck and their successors, but, except as
modified by the successors of Andrew Ross (Schrœder’s form), it is, I
believe, admitted that it has been superseded by other modifications lately
introduced into the Ross-Jackson instrument.
The year 1830 was, however, a propitious period in the history of the
modern microscope, as in January of that year Mr. Lister published his
epoch-making paper, “On the Improvement of the Achromatic
Microscope.” This appeared together with certain personal practical
directions (for no man was ever more anxious to communicate his
knowledge than Mr. Lister) to the before-mentioned opticians, which led up
to changes lasting until 1840, when, by the efforts of this gentleman and his
personal friends, “The Microscopical Society of London” came into
existence. Among the more prominent members of the Society was Mr.
George Jackson, a name still well known to microscopists, and who, jointly
with Mr. Lister, gave us the Jackson-Lister form of microscope. This was
forthwith accepted as a perfect model. Soon after Andrew Ross effected a
further change in the instrument, shown in Fig. 54 in its complete form as
left by this optician. It is here represented as having a bar movement, with a
claw foot bolted to two uprights to carry the trunnions with the body and
stage. This base, is insufficiently wide and extended to carry so large an
instrument with its centre of gravity so high. The coarse adjustment bar also
was rectangular, and the fine adjustment a lever, with the milled head in the
middle of the bar, which involved a certain amount of tremor; withal it was
an instrument of excellent workmanship, and its defects were not regarded
as irremediable. Messrs. Ross, however, preferred to construct an entirely
new model designed by Zentmayer, the “Ross-Jackson-Zentmayer,” to
which I shall refer presently. A later model, however, has to some extent
taken its place, “the Histological and Bacteriological Microscope,” Fig. 55.
extreme delicacy of focussing is an essential element.
The rival system of fine adjustment—the short lever and screw applied
externally to the body-tube—known as the Lister-Jackson system, which
appears to have been contrived to allow the body-tube to be supported more
firmly on the limb or stem, has had its merits ably realised in the
microscopes of Smith and Beck and their successors, but, except as
modified by the successors of Andrew Ross (Schrœder’s form), it is, I
believe, admitted that it has been superseded by other modifications lately
introduced into the Ross-Jackson instrument.
The year 1830 was, however, a propitious period in the history of the
modern microscope, as in January of that year Mr. Lister published his
epoch-making paper, “On the Improvement of the Achromatic
Microscope.” This appeared together with certain personal practical
directions (for no man was ever more anxious to communicate his
knowledge than Mr. Lister) to the before-mentioned opticians, which led up
to changes lasting until 1840, when, by the efforts of this gentleman and his
personal friends, “The Microscopical Society of London” came into
existence. Among the more prominent members of the Society was Mr.
George Jackson, a name still well known to microscopists, and who, jointly
with Mr. Lister, gave us the Jackson-Lister form of microscope. This was
forthwith accepted as a perfect model. Soon after Andrew Ross effected a
further change in the instrument, shown in Fig. 54 in its complete form as
left by this optician. It is here represented as having a bar movement, with a
claw foot bolted to two uprights to carry the trunnions with the body and
stage. This base, is insufficiently wide and extended to carry so large an
instrument with its centre of gravity so high. The coarse adjustment bar also
was rectangular, and the fine adjustment a lever, with the milled head in the
middle of the bar, which involved a certain amount of tremor; withal it was
an instrument of excellent workmanship, and its defects were not regarded
as irremediable. Messrs. Ross, however, preferred to construct an entirely
new model designed by Zentmayer, the “Ross-Jackson-Zentmayer,” to
which I shall refer presently. A later model, however, has to some extent
taken its place, “the Histological and Bacteriological Microscope,” Fig. 55.
Page 121
Fig. 54.—An early Ross-Jackson Microscope.
My reference to the older form of instrument is chiefly with the view of
directing attention to the sensitive focussing system, applied in the first
instance to the nose-piece; now placed below the coarse adjustment. It
certainly is a delicate form of fine adjustment. This model possesses other
points of interest well worth preserving, which fully entitle it to occupy the
prominent place given in the list of the house of Ross. In the Ross-Jackson
“Histological and Bacteriological Microscope” much attention seems to
have been given to eliminate certain weak points in the earlier Ross-Jackson
model—defects still extant in stands of certain English and foreign makers
—while retaining the more practical improvements of both constructions.
Steadiness is secured by an extension of the tripod or claw-foot and the
My reference to the older form of instrument is chiefly with the view of
directing attention to the sensitive focussing system, applied in the first
instance to the nose-piece; now placed below the coarse adjustment. It
certainly is a delicate form of fine adjustment. This model possesses other
points of interest well worth preserving, which fully entitle it to occupy the
prominent place given in the list of the house of Ross. In the Ross-Jackson
“Histological and Bacteriological Microscope” much attention seems to
have been given to eliminate certain weak points in the earlier Ross-Jackson
model—defects still extant in stands of certain English and foreign makers
—while retaining the more practical improvements of both constructions.
Steadiness is secured by an extension of the tripod or claw-foot and the
Page 122
shorter and more solid uprights that sustain the whole weight of the
instrument.
Fig. 55.—The Ross-Jackson Histological Microscope.
instrument.
Fig. 55.—The Ross-Jackson Histological Microscope.
Page 123
Fig. 56.—Powell and Lealand’s Students’ Microscope, with Amici prism arranged
for oblique illumination, the Sub-stage and Condenser being detached.
The Ross-Jackson, then, survives, together with the original tripod stand of
Hugh Powell’s, upon which he expended all the resources of the practical
optician, and applied the early principles involved in the Lister-Jackson
instrument, but from different points of view. However, there is hardly a
choice between one and the other in workmanship, both opticians having
furnished microscopes of a typical class and very high order. The firm of
Powell and Lealand have but one form of stand, from which they have
never been tempted to deviate. It is supported on a true tripod base, forming
a solid and substantial support to the body, which is of such a length as to
give as nearly as possible the standard optical interval of 10 inches between
the posterior principal focus of the objective and the anterior focus of the
eye-piece; the variation in the optical tube length does not exceed a quarter
for oblique illumination, the Sub-stage and Condenser being detached.
The Ross-Jackson, then, survives, together with the original tripod stand of
Hugh Powell’s, upon which he expended all the resources of the practical
optician, and applied the early principles involved in the Lister-Jackson
instrument, but from different points of view. However, there is hardly a
choice between one and the other in workmanship, both opticians having
furnished microscopes of a typical class and very high order. The firm of
Powell and Lealand have but one form of stand, from which they have
never been tempted to deviate. It is supported on a true tripod base, forming
a solid and substantial support to the body, which is of such a length as to
give as nearly as possible the standard optical interval of 10 inches between
the posterior principal focus of the objective and the anterior focus of the
eye-piece; the variation in the optical tube length does not exceed a quarter
Page 124
of an inch with objectives of ½ inch and upwards. The arm on which the
body is fixed is 5¾ inches long, which not only gives a clearance of 3½
inches from the optic axis, but also permits of the introduction of a long
fine-adjustment lever.
Fig. 57.—Powell’s larger No. 2 Instrument.
body is fixed is 5¾ inches long, which not only gives a clearance of 3½
inches from the optic axis, but also permits of the introduction of a long
fine-adjustment lever.
Fig. 57.—Powell’s larger No. 2 Instrument.
Page 125
Fig. 58.—Powell and Lealand’s Students’ Microscope arranged for direct
illumination. A. Secondary or Sub-stage racked up to bring the Achromatic
Condenser close to the object.
The cross arm encloses the lever mechanism for the fine adjustment, as
originally devised by Andrew Ross. This cross arm is longer than that used
by Ross, and carries the body more forward, so as to provide radial space
for the complete rotation of the stage and the optic axis, and at the same
time the lever of the adjustment is lengthened, and delicacy of motion
secured. The stage retains the mechanical movements invented by E.
Turrell, and first applied by Hugh Powell. It also rotates completely by
means of an obliquely placed pinion acting on a bevelled rack on the inner
face of the stage-ring supporting the mechanism. Finders are engraved on
the plates, and the main support of the stage-ring is graduated for angle
measuring, a pointer on the ring marking the unit of motion in arc.
The sub-stage is carried by rack-work, and has rectangular centring
movements, supporting an inner socket that can be rotated by rack and
pinion, and which carries the several sub-stage accessories. A fine
adjustment, by screw-cone and stud, is applied by means of an extra slide.
illumination. A. Secondary or Sub-stage racked up to bring the Achromatic
Condenser close to the object.
The cross arm encloses the lever mechanism for the fine adjustment, as
originally devised by Andrew Ross. This cross arm is longer than that used
by Ross, and carries the body more forward, so as to provide radial space
for the complete rotation of the stage and the optic axis, and at the same
time the lever of the adjustment is lengthened, and delicacy of motion
secured. The stage retains the mechanical movements invented by E.
Turrell, and first applied by Hugh Powell. It also rotates completely by
means of an obliquely placed pinion acting on a bevelled rack on the inner
face of the stage-ring supporting the mechanism. Finders are engraved on
the plates, and the main support of the stage-ring is graduated for angle
measuring, a pointer on the ring marking the unit of motion in arc.
The sub-stage is carried by rack-work, and has rectangular centring
movements, supporting an inner socket that can be rotated by rack and
pinion, and which carries the several sub-stage accessories. A fine
adjustment, by screw-cone and stud, is applied by means of an extra slide.
Page 126
The stage is attached to the sheath of the stem by a special arrangement of
screws, by which the rotation in the optic axis can be centred; sliding spring
clips and a movable and a removable and adjustable angle-piece to hold the
slides are applied on the upper surface. The body-tube is pivoted to move
laterally on the top of the stem, and an adjustable steel stud beneath serves
to stop the movement in the axis. Such is Powell’s present instrument, and it
represents the results of sixty years’ steady devotion to secure perfection,
and at the same time embody the best ideas of mechanical design by
Andrew Ross.
A cheaper form of students’ microscope is furnished by Powell and
Lealand, with ¾-inch stage movement, coarse and fine adjustments to body,
plane and concave mirrors, revolving diaphragm, two eye-pieces, and
Lister’s dark wells. These makers also adopt a gauge of tubing, the size
being such that it will take in a binocular body, a Huyghenian 2 inch eye-
piece having the largest field-glass possible. The tube of the sub-stage is the
same size, so as to secure one gauge of tubing throughout. This allows of a
Kellner or other eye-piece to be used as a condenser.
Ross’s Microscopes.
Messrs. Ross have more recently introduced several changes and
modifications in the Zentmayer stand, all tending to improve it, so that the
Ross-Zentmayer model takes its place as a first-class microscope.
Messrs. Ross have lately manufactured other forms of microscopes; one
especially designed for those commencing the study of bacteriology (Fig.
59). This instrument is one of the steadiest among those lately constructed
for high-class work. The circular foot and short stout pillar support the
whole instrument, and a substantial knee-joint sustains the full weight in the
upright or inclined positions, while the centre of gravity is by no means
disturbed, and absolute steadiness secured. The stage is of the horse-shoe
form, which affords convenient space for the fingers to lift the slide up
while the oil is placed in contact with the objective. The fine adjustment is
extremely sensitive, working smoothly and direct; this is entirely covered,
to prevent injury by dust. The micrometer screw works directly in the centre
screws, by which the rotation in the optic axis can be centred; sliding spring
clips and a movable and a removable and adjustable angle-piece to hold the
slides are applied on the upper surface. The body-tube is pivoted to move
laterally on the top of the stem, and an adjustable steel stud beneath serves
to stop the movement in the axis. Such is Powell’s present instrument, and it
represents the results of sixty years’ steady devotion to secure perfection,
and at the same time embody the best ideas of mechanical design by
Andrew Ross.
A cheaper form of students’ microscope is furnished by Powell and
Lealand, with ¾-inch stage movement, coarse and fine adjustments to body,
plane and concave mirrors, revolving diaphragm, two eye-pieces, and
Lister’s dark wells. These makers also adopt a gauge of tubing, the size
being such that it will take in a binocular body, a Huyghenian 2 inch eye-
piece having the largest field-glass possible. The tube of the sub-stage is the
same size, so as to secure one gauge of tubing throughout. This allows of a
Kellner or other eye-piece to be used as a condenser.
Ross’s Microscopes.
Messrs. Ross have more recently introduced several changes and
modifications in the Zentmayer stand, all tending to improve it, so that the
Ross-Zentmayer model takes its place as a first-class microscope.
Messrs. Ross have lately manufactured other forms of microscopes; one
especially designed for those commencing the study of bacteriology (Fig.
59). This instrument is one of the steadiest among those lately constructed
for high-class work. The circular foot and short stout pillar support the
whole instrument, and a substantial knee-joint sustains the full weight in the
upright or inclined positions, while the centre of gravity is by no means
disturbed, and absolute steadiness secured. The stage is of the horse-shoe
form, which affords convenient space for the fingers to lift the slide up
while the oil is placed in contact with the objective. The fine adjustment is
extremely sensitive, working smoothly and direct; this is entirely covered,
to prevent injury by dust. The micrometer screw works directly in the centre
Page 127
of its fittings, the milled head being divided to read to 1⁄500 of an inch. The
sub-stage is fitted with a new centring coarse and fine adjustment, so that
when using high powers with the Abbe condenser accurate focus can be
secured with the least amount of trouble.
Fig. 59.—Ross’s “Bacteriological and Histological” Microscope.
The amount of activity shown during the last few years by opticians in the
manufacture of new forms of microscopes renders it somewhat difficult to
keep pace with improvements, some of which are novel. A further source of
congratulation is that economy has all along been studied; so much so, that
the instruments in question are within the reach of persons of moderate
means. Messrs. Ross and Co. have taken a new departure in this respect,
and their “Eclipse” Microscope is an entirely new form of stand with a ring
foot. This microscope has been produced for the especial use of students,
sub-stage is fitted with a new centring coarse and fine adjustment, so that
when using high powers with the Abbe condenser accurate focus can be
secured with the least amount of trouble.
Fig. 59.—Ross’s “Bacteriological and Histological” Microscope.
The amount of activity shown during the last few years by opticians in the
manufacture of new forms of microscopes renders it somewhat difficult to
keep pace with improvements, some of which are novel. A further source of
congratulation is that economy has all along been studied; so much so, that
the instruments in question are within the reach of persons of moderate
means. Messrs. Ross and Co. have taken a new departure in this respect,
and their “Eclipse” Microscope is an entirely new form of stand with a ring
foot. This microscope has been produced for the especial use of students,
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and can be purchased for a moderate sum. It will be seen at a glance (Fig.
60) how steady this form of stand must necessarily be, since the centre of
gravity is secured in every direction and inclination. The body-tube carries
eye-pieces, numbered, of the Continental size and optical tube-length (160
mm.), for which the object glasses are adjusted, and a draw-tube extending
to eight inches.
The fine adjustment is independent
of set screws, and not subject to
derangement. It is extremely
sensitive and direct in action, and
from its construction is equal in
perfection of working to the best that
can be made. Its fitting, by a new
contrivance, is completely covered at
all points, being thus preserved from
disturbance or injury by dust.
The Eclipse is furnished with two
eye-pieces, 1′′ and ¼′′ object glasses
of highest excellence and large
angular aperture, both adjusted to a
double nose-piece, so that they focus
in the same plane; and a swinging
mirror and stage iris diaphragm.
In “Wenham’s Radial” Microscope
the chief aim has been directed
towards providing a very
considerable range of effects, both in
Fig. 60.—Ross’s Rigid Pattern “Eclipse”
Microscope. altitude and azimuth. The leading
principle followed throughout in the
construction of this form of stand is that of facilitating the work of the
microscopist and of obtaining the maximum range of oblique illumination
in all directions. This is fairly well attained by causing all the movements of
inclination and rotation to radiate from the object as a common centre. Thus
it has been found possible to combine seven radial motions, so that when
60) how steady this form of stand must necessarily be, since the centre of
gravity is secured in every direction and inclination. The body-tube carries
eye-pieces, numbered, of the Continental size and optical tube-length (160
mm.), for which the object glasses are adjusted, and a draw-tube extending
to eight inches.
The fine adjustment is independent
of set screws, and not subject to
derangement. It is extremely
sensitive and direct in action, and
from its construction is equal in
perfection of working to the best that
can be made. Its fitting, by a new
contrivance, is completely covered at
all points, being thus preserved from
disturbance or injury by dust.
The Eclipse is furnished with two
eye-pieces, 1′′ and ¼′′ object glasses
of highest excellence and large
angular aperture, both adjusted to a
double nose-piece, so that they focus
in the same plane; and a swinging
mirror and stage iris diaphragm.
In “Wenham’s Radial” Microscope
the chief aim has been directed
towards providing a very
considerable range of effects, both in
Fig. 60.—Ross’s Rigid Pattern “Eclipse”
Microscope. altitude and azimuth. The leading
principle followed throughout in the
construction of this form of stand is that of facilitating the work of the
microscopist and of obtaining the maximum range of oblique illumination
in all directions. This is fairly well attained by causing all the movements of
inclination and rotation to radiate from the object as a common centre. Thus
it has been found possible to combine seven radial motions, so that when
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the instrument is inclined backwards, as in Fig. 61, or placed in the
horizontal, as in Fig. 62 or rotated from in the brass plate, a pencil of light
from a fixed source shall always reach the object and pass to the objective.
The stage is made to rotate completely, and its rectangular motions are
effected by milled heads acting entirely within the circumference. The sub-
stage is mounted on the Zentmayer system, with two centring screws, by
means of which the optic axis is secured. It is also provided with
rectangular and rotating motions. The coarse adjustment is that of the Ross-
Jackson form—a spiral pinion and diagonal rackwork, while the fine is on
an entirely new principle designed by Dr. H. Schrœder.
The “Ross-Zentmayer Microscope”
is a thoroughly substantial and
practical instrument, combining
elegance of appearance with strength
and firmness.
It is a true tripod model, consisting
of a triangular base with two pillars
rising from a cross-piece, which
carries the trunnions. The slow
movement is obtained by a second
slide close behind the first; but to
avoid the friction of rubbing
surfaces, hardened steel rollers are
inserted between them, which give a Fig. 61.—Ross’s Wenham Radial Microscope.
frictionless fine motion, amenable to
the slightest touch of the milled-head
screw situated conveniently at the
back of the limb, through which a
steel lever passes which actuates the
slow motion slide. The body of the
instrument is therefore not touched
during the fine focussing, so that all
lateral movement is avoided. The
mechanical stage rotates axially, and
the outer edge of the lower plate is
horizontal, as in Fig. 62 or rotated from in the brass plate, a pencil of light
from a fixed source shall always reach the object and pass to the objective.
The stage is made to rotate completely, and its rectangular motions are
effected by milled heads acting entirely within the circumference. The sub-
stage is mounted on the Zentmayer system, with two centring screws, by
means of which the optic axis is secured. It is also provided with
rectangular and rotating motions. The coarse adjustment is that of the Ross-
Jackson form—a spiral pinion and diagonal rackwork, while the fine is on
an entirely new principle designed by Dr. H. Schrœder.
The “Ross-Zentmayer Microscope”
is a thoroughly substantial and
practical instrument, combining
elegance of appearance with strength
and firmness.
It is a true tripod model, consisting
of a triangular base with two pillars
rising from a cross-piece, which
carries the trunnions. The slow
movement is obtained by a second
slide close behind the first; but to
avoid the friction of rubbing
surfaces, hardened steel rollers are
inserted between them, which give a Fig. 61.—Ross’s Wenham Radial Microscope.
frictionless fine motion, amenable to
the slightest touch of the milled-head
screw situated conveniently at the
back of the limb, through which a
steel lever passes which actuates the
slow motion slide. The body of the
instrument is therefore not touched
during the fine focussing, so that all
lateral movement is avoided. The
mechanical stage rotates axially, and
the outer edge of the lower plate is
Page 130
divided into degrees, in order to Fig. 62.—The Ross-Wenham Radial Microscope.
register the angles; a simple mode of
adjustment is provided for setting the centre of rotation exactly coincident
with the focal point of the objective. As the plates of the stage have no
screw or rackwork between them (these are placed externally), they are
brought close together, thus affording the advantage of a thin substantial
stage, and ensuring rigidity where most required; phosphor-bronze being
used in its construction. The stage is attached to the limb by a conical stem,
with a screw and clamp nut at the back, so that it can be easily removed for
the substitution of a simple plate or other stage; by turning the stem in the
socket the stage may be tilted sideways at any angle required. A feature in
the Ross-Zentmayer stand is the swinging sub-stage and bar carrying the
mirror, having its axis of rotation situated from an axial point in the plane of
the object, which consequently receives the light without requiring
alteration of focus in any position of the bar; by this means facilities are
afforded for the resolution of objects requiring oblique light and for the
development of their structure. Rays are thus obtained from any angle and
indicated by the graduated circle round the top of the swing-bar, and many
troublesome and expensive pieces of sub-stage apparatus dispensed with.
The value of this arrangement was long ago recognised in Grubb’s “Sector
Stand,” the movement of which was obtained in a far less efficient manner.
register the angles; a simple mode of
adjustment is provided for setting the centre of rotation exactly coincident
with the focal point of the objective. As the plates of the stage have no
screw or rackwork between them (these are placed externally), they are
brought close together, thus affording the advantage of a thin substantial
stage, and ensuring rigidity where most required; phosphor-bronze being
used in its construction. The stage is attached to the limb by a conical stem,
with a screw and clamp nut at the back, so that it can be easily removed for
the substitution of a simple plate or other stage; by turning the stem in the
socket the stage may be tilted sideways at any angle required. A feature in
the Ross-Zentmayer stand is the swinging sub-stage and bar carrying the
mirror, having its axis of rotation situated from an axial point in the plane of
the object, which consequently receives the light without requiring
alteration of focus in any position of the bar; by this means facilities are
afforded for the resolution of objects requiring oblique light and for the
development of their structure. Rays are thus obtained from any angle and
indicated by the graduated circle round the top of the swing-bar, and many
troublesome and expensive pieces of sub-stage apparatus dispensed with.
The value of this arrangement was long ago recognised in Grubb’s “Sector
Stand,” the movement of which was obtained in a far less efficient manner.
Page 131
Fig. 63.—The Improved Ross-Zentmayer Model.
The base or foot of the Ross-Zentmayer instrument is made in one piece.
Preference must be given to the double pillar support, as this is firmer, and
allows the sub-stage to swing free while the microscope is in a vertical
position, as in working with fluid preparations. The sub-stage is provided
with screws for centring, and, when determined, secured by a clamping
screw.
The sub-stage, with its apparatus in place, can be instantly removed, by
being drawn out sideways, so as to use the mirror alone, which is a great
convenience.
The mechanical movements of this instrument are perfect, and well adapted
to their purpose.
The base or foot of the Ross-Zentmayer instrument is made in one piece.
Preference must be given to the double pillar support, as this is firmer, and
allows the sub-stage to swing free while the microscope is in a vertical
position, as in working with fluid preparations. The sub-stage is provided
with screws for centring, and, when determined, secured by a clamping
screw.
The sub-stage, with its apparatus in place, can be instantly removed, by
being drawn out sideways, so as to use the mirror alone, which is a great
convenience.
The mechanical movements of this instrument are perfect, and well adapted
to their purpose.
Page 132
Messrs. Ross have other typical forms of microscopes. Their “New
Industrial” Microscope, for the use of farmers, horticulturists, textile and
other trades, for the examination of produce and raw materials, is a
surprisingly cheap one, and deserving of commendation. The great utility of
microscopical research to purposes of advanced agriculture is fully
recognised, and a less costly instrument than that usually supplied for more
complex investigations was much needed. It is provided with a broad
square stage for the purpose of receiving a glass dish to contain liquids or
manifold objects, and which may be moved on the stage to bring the
various particles under observation. A fitting beneath the stage carries a
plate with diaphragm apertures for modifying the light, and as seeds, textile
fibres, and other opaque objects form a large portion of those to be
examined, this sub-stage plate has a space between the perforations which,
when brought into position, provides a dark ground by preventing the
passage of light from underneath. A condensing lens is, however, provided
for the better lighting of opaque objects. Here we have a microscope which
combines efficiency with stability, while its very simplification allows of a
really good and effective instrument for the small sum of £3 3s.
Industrial” Microscope, for the use of farmers, horticulturists, textile and
other trades, for the examination of produce and raw materials, is a
surprisingly cheap one, and deserving of commendation. The great utility of
microscopical research to purposes of advanced agriculture is fully
recognised, and a less costly instrument than that usually supplied for more
complex investigations was much needed. It is provided with a broad
square stage for the purpose of receiving a glass dish to contain liquids or
manifold objects, and which may be moved on the stage to bring the
various particles under observation. A fitting beneath the stage carries a
plate with diaphragm apertures for modifying the light, and as seeds, textile
fibres, and other opaque objects form a large portion of those to be
examined, this sub-stage plate has a space between the perforations which,
when brought into position, provides a dark ground by preventing the
passage of light from underneath. A condensing lens is, however, provided
for the better lighting of opaque objects. Here we have a microscope which
combines efficiency with stability, while its very simplification allows of a
really good and effective instrument for the small sum of £3 3s.
Page 133
Fig. 64.—Ross’s “New Industrial” Microscope.
Messrs. Beck’s Microscopes.
Messrs. Beck have adopted what may be termed a rival system of fine
adjustment in their modern microscopes. The short lever and screw applied
externally to the body tube is peculiar, I may say, to the Ross-Jackson
system, and was originally devised to allow of the body tube being
supported somewhat more firmly on the limb. This change had its merits
fully realised in the early microscopes of Smith and Beck. To their
successors, R. & J. Beck, the microscope owes much, and very many
important improvements, while all their instruments and accessories are
excellent examples of good workmanship and finish. In their Pathological
Messrs. Beck’s Microscopes.
Messrs. Beck have adopted what may be termed a rival system of fine
adjustment in their modern microscopes. The short lever and screw applied
externally to the body tube is peculiar, I may say, to the Ross-Jackson
system, and was originally devised to allow of the body tube being
supported somewhat more firmly on the limb. This change had its merits
fully realised in the early microscopes of Smith and Beck. To their
successors, R. & J. Beck, the microscope owes much, and very many
important improvements, while all their instruments and accessories are
excellent examples of good workmanship and finish. In their Pathological
Page 134
Microscope we have a movement originally found in Tolles’ microscopes: a
vertical disc, by which the centre can be raised or depressed to correspond
with the thickness of the slide. The stage can also be brought into an
inverted position by rack and pinion. Their fine adjustment has been greatly
improved, as we shall presently see, whereby it has been made more
sensitive and delicate of adjustment. The general construction of their
microscopes as a rule possess the following advantages: the stands are
strong, firm, and yet not too light or too heavy, the instruments cannot alter
from the position in which they are placed, as, unfortunately, will
occasionally happen when joints work loose; in every position the heavier
part of the stand maintains the centre of gravity.
Beck’s Pathological Microscope (Fig. 65) is a nearly perfect instrument,
furnished with a firm triangular foot, which ensures great steadiness in any
position. It has a well adapted joint for placing the instrument at any angle
of inclination; coarse adjustment by spiral rack and pinion; fine adjustment
by delicate lever and micrometer screw motion; rack and pinion focussing
and screw centring sub-stage, made to carry all condensers and other sub-
stage apparatus; mechanical stage with horizontal and vertical traversing
motions. The stage is attached to the instrument by two screws and can
therefore be removed at pleasure, leaving a large square flat glass stage for
the culture-plate. It is likewise provided with finder divisions, and as it
always fits on to the same place, any particular portion of the object can be
recorded and found at any moment. The triple nose-piece is a convenient
addition, and a very acceptable one to the student while diligently engaged
in histological research.
vertical disc, by which the centre can be raised or depressed to correspond
with the thickness of the slide. The stage can also be brought into an
inverted position by rack and pinion. Their fine adjustment has been greatly
improved, as we shall presently see, whereby it has been made more
sensitive and delicate of adjustment. The general construction of their
microscopes as a rule possess the following advantages: the stands are
strong, firm, and yet not too light or too heavy, the instruments cannot alter
from the position in which they are placed, as, unfortunately, will
occasionally happen when joints work loose; in every position the heavier
part of the stand maintains the centre of gravity.
Beck’s Pathological Microscope (Fig. 65) is a nearly perfect instrument,
furnished with a firm triangular foot, which ensures great steadiness in any
position. It has a well adapted joint for placing the instrument at any angle
of inclination; coarse adjustment by spiral rack and pinion; fine adjustment
by delicate lever and micrometer screw motion; rack and pinion focussing
and screw centring sub-stage, made to carry all condensers and other sub-
stage apparatus; mechanical stage with horizontal and vertical traversing
motions. The stage is attached to the instrument by two screws and can
therefore be removed at pleasure, leaving a large square flat glass stage for
the culture-plate. It is likewise provided with finder divisions, and as it
always fits on to the same place, any particular portion of the object can be
recorded and found at any moment. The triple nose-piece is a convenient
addition, and a very acceptable one to the student while diligently engaged
in histological research.
Page 135
Fig. 65.—Beck’s Pathological Microscope, with square and removable stage.
Page 136
Fig. 66.—Beck’s Large “Continental Model” Microscope.
Beck’s Large “Continental Model” Microscope is of superior finish. It is
provided with a substantial horse-shoe foot, which gives support to the
strong, well-balanced body, jointed for giving the microscope any angle of
inclination. The body is provided with a draw-tube which can be racked
down to the Continental measurement. It has a spiral rack and pinion coarse
adjustment, and a fine adjustment of the most perfect workmanship, which
will be described in detail presently. It has a large square stage with
vulcanite top plate to receive culture preparations. The sub-stage is of the
most approved form for centring, and carries an achromatic or Abbe
condenser, iris diaphragm, &c. The double mirror can be swung out of place
for direct illumination and micro-photography. Altogether, this instrument is
in every way fitted for critical or class-room work.
Beck’s Large “Continental Model” Microscope is of superior finish. It is
provided with a substantial horse-shoe foot, which gives support to the
strong, well-balanced body, jointed for giving the microscope any angle of
inclination. The body is provided with a draw-tube which can be racked
down to the Continental measurement. It has a spiral rack and pinion coarse
adjustment, and a fine adjustment of the most perfect workmanship, which
will be described in detail presently. It has a large square stage with
vulcanite top plate to receive culture preparations. The sub-stage is of the
most approved form for centring, and carries an achromatic or Abbe
condenser, iris diaphragm, &c. The double mirror can be swung out of place
for direct illumination and micro-photography. Altogether, this instrument is
in every way fitted for critical or class-room work.
Page 137
To return to the fine adjustment of this, as
of other forms of Messrs. Beck’s
microscopes, the applied mechanism of
which is believed to be one of the most
sensitive and delicate character yet
contrived. It is constructed as shown in the
accompanying figure. The body of the
instrument is supported upon the barrel D
D; this barrel is accurately and smoothly
fitted to the triangular core E E. At the top
of barrel D D is screwed the cap G, to
which is attached the rod C; this rod passes
through the centre of the core E E and
connects with the lever arm A at B. The
action of the spring J, which is wrapped
spirally around the rod C, raises the body
of the microscope and holds the lever arm
A tightly against the screw arm F. The
slightest motion, therefore, of the screw F
is communicated through the lever A and
the rod C to the body of the microscope.
Fig. 67.—Beck’s “New Fine Adjustment.” The great delicacy of this arrangement will
be appreciated when it is noticed that the
distance from I H is double the distance of I B, therefore any motion at B is
only half that at H. This adjustment is one of the most delicate made for use
with high powers.
of other forms of Messrs. Beck’s
microscopes, the applied mechanism of
which is believed to be one of the most
sensitive and delicate character yet
contrived. It is constructed as shown in the
accompanying figure. The body of the
instrument is supported upon the barrel D
D; this barrel is accurately and smoothly
fitted to the triangular core E E. At the top
of barrel D D is screwed the cap G, to
which is attached the rod C; this rod passes
through the centre of the core E E and
connects with the lever arm A at B. The
action of the spring J, which is wrapped
spirally around the rod C, raises the body
of the microscope and holds the lever arm
A tightly against the screw arm F. The
slightest motion, therefore, of the screw F
is communicated through the lever A and
the rod C to the body of the microscope.
Fig. 67.—Beck’s “New Fine Adjustment.” The great delicacy of this arrangement will
be appreciated when it is noticed that the
distance from I H is double the distance of I B, therefore any motion at B is
only half that at H. This adjustment is one of the most delicate made for use
with high powers.
Page 138
Fig. 68.—Beck’s National Binocular Microscope.
In the construction of Beck’s Binocular National Microscope, the body is
held in a sliding fitting in the limb, and is moved up or down by means of a
rack and pinion motion. This constitutes the coarse focussing adjustment.
The fine adjustment is effected by the milled head, which acts upon the
body by means of a lever inside the limb. The upper circular surface of the
stage is made of glass, and carries the object holder, which is provided with
a ledge and spring to hold the object by means of the pressure of an ivory-
tipped screw, so that it can be moved about readily and smoothly. The
pressure of the screw is adjusted by the milled head, which permits of more
or less pressure being made upon the edge of the object.
In the construction of Beck’s Binocular National Microscope, the body is
held in a sliding fitting in the limb, and is moved up or down by means of a
rack and pinion motion. This constitutes the coarse focussing adjustment.
The fine adjustment is effected by the milled head, which acts upon the
body by means of a lever inside the limb. The upper circular surface of the
stage is made of glass, and carries the object holder, which is provided with
a ledge and spring to hold the object by means of the pressure of an ivory-
tipped screw, so that it can be moved about readily and smoothly. The
pressure of the screw is adjusted by the milled head, which permits of more
or less pressure being made upon the edge of the object.
Page 139
Fig. 69.—Beck’s Star Microscope.
When the stage is required for other purposes the object holder can be
unscrewed and removed. Beneath the stage there is a cylindrical fitting for
the reception of a diaphragm, a polariser, or other apparatus. The mirror,
besides swinging in a rotatory semi-circle, is made to slide up or down the
stem. The microscope is supported by a firm pillar on a tripod base, and the
body can be inclined at any angle convenient for working. A sub-stage can
be added at any time for the reception of an achromatic condenser fitted
with concentric screws—a necessity for more delicate microscopical
research work.
Beck’s Star Microscope is in every sense a students’ or class-room
instrument. It is firm and well made, with joint for inclination, large square
stage, sliding coarse adjustment and fine adjustment by micrometer screw,
When the stage is required for other purposes the object holder can be
unscrewed and removed. Beneath the stage there is a cylindrical fitting for
the reception of a diaphragm, a polariser, or other apparatus. The mirror,
besides swinging in a rotatory semi-circle, is made to slide up or down the
stem. The microscope is supported by a firm pillar on a tripod base, and the
body can be inclined at any angle convenient for working. A sub-stage can
be added at any time for the reception of an achromatic condenser fitted
with concentric screws—a necessity for more delicate microscopical
research work.
Beck’s Star Microscope is in every sense a students’ or class-room
instrument. It is firm and well made, with joint for inclination, large square
stage, sliding coarse adjustment and fine adjustment by micrometer screw,
Page 140
draw-tube, iris diaphragm, double mirror on swinging crank arm, A or B
eye-piece, a one-inch and quarter-inch objective, the magnifying power of
which ranges from 38·5 to 183.
Fig. 70.—Beck’s Binocular Dissecting Microscope.
An early binocular microscope for dissecting purposes was devised by the
late Mr. R. Beck. (Fig. 70.) This took the form of a simple instrument built
up on a square mahogany base A raised about four inches upon four brass
supports B B, having a large circular stage plate made to revolve on a
second plate, on which the object is placed and brought under the eye for
dissection. On the left hand side is a milled head rack and pinion K, which
acts upon a horizontal bar I for focussing the magnifying lens. Another bar,
R, carries the prism P and a pair of eye-pieces arranged on the principle of
M. Nachet’s binocular microscope. Mr. Beck preferred to adopt Wenham’s
method of arranging these prisms; that is, by allowing half the cone of rays
to proceed to one eye without interruption, while the other half is
eye-piece, a one-inch and quarter-inch objective, the magnifying power of
which ranges from 38·5 to 183.
Fig. 70.—Beck’s Binocular Dissecting Microscope.
An early binocular microscope for dissecting purposes was devised by the
late Mr. R. Beck. (Fig. 70.) This took the form of a simple instrument built
up on a square mahogany base A raised about four inches upon four brass
supports B B, having a large circular stage plate made to revolve on a
second plate, on which the object is placed and brought under the eye for
dissection. On the left hand side is a milled head rack and pinion K, which
acts upon a horizontal bar I for focussing the magnifying lens. Another bar,
R, carries the prism P and a pair of eye-pieces arranged on the principle of
M. Nachet’s binocular microscope. Mr. Beck preferred to adopt Wenham’s
method of arranging these prisms; that is, by allowing half the cone of rays
to proceed to one eye without interruption, while the other half is
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intercepted by the prisms and transmitted to the other eye. Beneath the stage
is the ordinary mirror L. The condensing lens M is supported on a separate
brass holder let into one of the supports of the stand. In practice, however,
this arrangement was found inconvenient, and the microscope has therefore
not been brought into general use.
Messrs. Watson’s Microscopes.
Among London opticians, the various microscopes manufactured by
Messrs. Watson, of Holborn, are of high finish and good workmanship.
Those specially designed for the use of students possess merits of their own
in their mechanical construction, and also embody a provision, as indeed do
all their instruments, whether for students or more pretentious work,
whereby wear and tear in their frictional parts can be compensated for by
the user himself. This is effected in a simple but efficient manner. The
fittings are sprung, and screws set just outside the dove-tails. The very
slightest turn of the screws compresses the dove-tails, and a very large
amount of wear can in this way be prevented.
I am glad to notice that Messrs. Watson have adopted certain standard sizes
recommended some time ago by the Royal Microscopical Society for the
diameters of eye-pieces. It would be a great advantage if the same standard
became generally recognised and brought into use, since it is a matter of
much importance to microscopists.
Watson’s Edinburgh Students’ Microscope (Fig. 71) is a thoroughly efficient
one for all practical purposes, great care having been bestowed upon its
smallest details, and it is not difficult to perceive the reason of its popularity
among students. The tripod form of foot ensures great steadiness and
firmness; the body carries the smaller 0·92 eye-piece, and with draw-tube
closed is of the Continental length. The draw-tube is graduated to
millimetres, and when fully extended the body measures 10 inches. The
stage is provided with mechanical and rotary movements; the compound
sub-stage with centring screws, rack and pinion to focus, and a means of
lifting the condenser out of the optical axis when not required for use.
Notwithstanding, none of the movements are at all cramped; a clear
is the ordinary mirror L. The condensing lens M is supported on a separate
brass holder let into one of the supports of the stand. In practice, however,
this arrangement was found inconvenient, and the microscope has therefore
not been brought into general use.
Messrs. Watson’s Microscopes.
Among London opticians, the various microscopes manufactured by
Messrs. Watson, of Holborn, are of high finish and good workmanship.
Those specially designed for the use of students possess merits of their own
in their mechanical construction, and also embody a provision, as indeed do
all their instruments, whether for students or more pretentious work,
whereby wear and tear in their frictional parts can be compensated for by
the user himself. This is effected in a simple but efficient manner. The
fittings are sprung, and screws set just outside the dove-tails. The very
slightest turn of the screws compresses the dove-tails, and a very large
amount of wear can in this way be prevented.
I am glad to notice that Messrs. Watson have adopted certain standard sizes
recommended some time ago by the Royal Microscopical Society for the
diameters of eye-pieces. It would be a great advantage if the same standard
became generally recognised and brought into use, since it is a matter of
much importance to microscopists.
Watson’s Edinburgh Students’ Microscope (Fig. 71) is a thoroughly efficient
one for all practical purposes, great care having been bestowed upon its
smallest details, and it is not difficult to perceive the reason of its popularity
among students. The tripod form of foot ensures great steadiness and
firmness; the body carries the smaller 0·92 eye-piece, and with draw-tube
closed is of the Continental length. The draw-tube is graduated to
millimetres, and when fully extended the body measures 10 inches. The
stage is provided with mechanical and rotary movements; the compound
sub-stage with centring screws, rack and pinion to focus, and a means of
lifting the condenser out of the optical axis when not required for use.
Notwithstanding, none of the movements are at all cramped; a clear
Page 142
distance is maintained beneath the stage, affording plenty of room for
manipulating the mirror. Both coarse and fine adjustments work with
smoothness, the latter being on Watson’s latest improved principle—one
revolution of the milled head moves the body 1⁄300 of an inch. The stage is of
extra large size, to allow of the use of large culture-plates. No Continental
stand of higher price compares with the Edinburgh microscope. Its height
when placed in the vertical position is 11½ inches.
Fig. 71.—Watson’s Edinburgh Students’ Microscope.
manipulating the mirror. Both coarse and fine adjustments work with
smoothness, the latter being on Watson’s latest improved principle—one
revolution of the milled head moves the body 1⁄300 of an inch. The stage is of
extra large size, to allow of the use of large culture-plates. No Continental
stand of higher price compares with the Edinburgh microscope. Its height
when placed in the vertical position is 11½ inches.
Fig. 71.—Watson’s Edinburgh Students’ Microscope.
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Fig. 72.—Sub-stage of Edinburgh Students’ Microscope. This view of underside of
stage of students’ instrument shows the mirror set at an angle for oblique
illumination, and sub-stage turned aside.
The various sizes of oculars adopted by opticians and at present in vogue
cause considerable confusion. A standard size is specially needed for
students’ and small microscopes. The standard long used by Continental
manufacturers is 0·92 of an inch. The adoption of this size would place the
eye-piece in the same position as that of the universal screw for the
objective, formulated by the Royal Microscopical Society many years ago.
The desirability of using standard sizes has been fully recognised by
Messrs. Watson and they are now adapted to most of their microscopes. The
English diameter, 1·35 of an inch, known as the “Ross” size, is retained in
all their microscopes of large size.
Watson’s Mechanical Draw-tube.
stage of students’ instrument shows the mirror set at an angle for oblique
illumination, and sub-stage turned aside.
The various sizes of oculars adopted by opticians and at present in vogue
cause considerable confusion. A standard size is specially needed for
students’ and small microscopes. The standard long used by Continental
manufacturers is 0·92 of an inch. The adoption of this size would place the
eye-piece in the same position as that of the universal screw for the
objective, formulated by the Royal Microscopical Society many years ago.
The desirability of using standard sizes has been fully recognised by
Messrs. Watson and they are now adapted to most of their microscopes. The
English diameter, 1·35 of an inch, known as the “Ross” size, is retained in
all their microscopes of large size.
Watson’s Mechanical Draw-tube.
Page 144
Fig. 73.—Watson’s Mechanical Draw-tube (full-size).
An important feature in connection with the body-tube of Watson’s
Edinburgh Students’ Microscope (as, indeed, in all their fully furnished
instruments) is that they are provided with two draw-tubes; one moved by
rack-work, the other sliding inside the body-tube. The advantage is, that the
body can be made very short or extremely long, while sufficient latitude can
be given to objectives corrected for either Continental or English tube-
lengths, and to adjusting the same for thickness of cover-glass by variation
of tube length. Should the cover-glass be thicker than that for which the
objective is corrected, a shorter tube-length is necessary; if thinner, the body
must be lengthened. This is effected by means of the rackwork draw-tube.
The length of the body when closed is 142 millimetres (55⁄8 inches), and
when the two draw-tubes are extended, 305 millimetres (12 inches), being,
An important feature in connection with the body-tube of Watson’s
Edinburgh Students’ Microscope (as, indeed, in all their fully furnished
instruments) is that they are provided with two draw-tubes; one moved by
rack-work, the other sliding inside the body-tube. The advantage is, that the
body can be made very short or extremely long, while sufficient latitude can
be given to objectives corrected for either Continental or English tube-
lengths, and to adjusting the same for thickness of cover-glass by variation
of tube length. Should the cover-glass be thicker than that for which the
objective is corrected, a shorter tube-length is necessary; if thinner, the body
must be lengthened. This is effected by means of the rackwork draw-tube.
The length of the body when closed is 142 millimetres (55⁄8 inches), and
when the two draw-tubes are extended, 305 millimetres (12 inches), being,
Page 145
therefore, shorter than the Continental and longer than the English tube
lengths. Both draw-tubes are divided into millimetres, and on the rackwork
draw-tube a double scale is engraved, reading continuously from the sliding
draw-tube when fully drawn out, or giving the body length when the
rackwork draw-tube alone is in use. The utility of this mechanical draw-
tube is that it permits of quick manipulation with perfect results.
Fig. 74.—Watson’s Histological Microscope. Stand “A.”—Height, when placed
vertically and tube pushed home, 9½ inches.
The inside top of the draw-tube is smaller than the remainder, the former
making a fitting for the eye-piece about 1 inch long, permitting of the tube
being blackened inside up to this fitting, thus minimising reflection. The
end of the draw-tube has the universal screw for using the apertometer, &c.
lengths. Both draw-tubes are divided into millimetres, and on the rackwork
draw-tube a double scale is engraved, reading continuously from the sliding
draw-tube when fully drawn out, or giving the body length when the
rackwork draw-tube alone is in use. The utility of this mechanical draw-
tube is that it permits of quick manipulation with perfect results.
Fig. 74.—Watson’s Histological Microscope. Stand “A.”—Height, when placed
vertically and tube pushed home, 9½ inches.
The inside top of the draw-tube is smaller than the remainder, the former
making a fitting for the eye-piece about 1 inch long, permitting of the tube
being blackened inside up to this fitting, thus minimising reflection. The
end of the draw-tube has the universal screw for using the apertometer, &c.
Page 146
Watson’s Histological Microscope (Fig. 74) is a somewhat cheaper form of
instrument, designed for the student; although of plainer construction it is
quite as well made as the costlier model. It is provided with spiral rack and
pinion coarse adjustment, and with this motion the greatest smoothness is
preserved. There is no backlash, the teeth of the pinion never leaving the
rack; so effective is it that a high power can be perfectly focussed by its
means. It is also furnished with their universal pattern of fine adjustment.
This can be had for £3 3s.
Fig. 75.—Watson’s Semi-Mechanical Stage.
Messrs. Watson have among other accessories of value introduced in
connection with their several microscopes a semi-mechanical stage,
whereby they are enabled to reduce the cost of manufacture. Fig. 75 is an
outline sketch of the same.
This stage is of the horse-shoe shape, with cut-out centre, constructed of ¼-
inch brass plate, and measures over all 5¼ inches wide by 4 inches deep.
Fitting on the edges of the main stage is a frame which is actuated vertically
by means of a double rack and pinion from beneath, giving ¾-inch of
movement, having controlling heads on either side of the stage; on the
edges of this mechanical frame a sliding bar is fitted, consequently
movement may be imparted either by rackwork or by hand. The mechanical
movement, however is in one direction only; but as the bar carries the
instrument, designed for the student; although of plainer construction it is
quite as well made as the costlier model. It is provided with spiral rack and
pinion coarse adjustment, and with this motion the greatest smoothness is
preserved. There is no backlash, the teeth of the pinion never leaving the
rack; so effective is it that a high power can be perfectly focussed by its
means. It is also furnished with their universal pattern of fine adjustment.
This can be had for £3 3s.
Fig. 75.—Watson’s Semi-Mechanical Stage.
Messrs. Watson have among other accessories of value introduced in
connection with their several microscopes a semi-mechanical stage,
whereby they are enabled to reduce the cost of manufacture. Fig. 75 is an
outline sketch of the same.
This stage is of the horse-shoe shape, with cut-out centre, constructed of ¼-
inch brass plate, and measures over all 5¼ inches wide by 4 inches deep.
Fitting on the edges of the main stage is a frame which is actuated vertically
by means of a double rack and pinion from beneath, giving ¾-inch of
movement, having controlling heads on either side of the stage; on the
edges of this mechanical frame a sliding bar is fitted, consequently
movement may be imparted either by rackwork or by hand. The mechanical
movement, however is in one direction only; but as the bar carries the
Page 147
object, the worker can easily move the object out horizontally with the
finger. The advantage of this stage is that the whole surface is perfectly
flush, and the pinion heads are below its level, so that culture plates or
continuous sections may be conveniently examined.
finger. The advantage of this stage is that the whole surface is perfectly
flush, and the pinion heads are below its level, so that culture plates or
continuous sections may be conveniently examined.
Page 148
Another addition of considerable value
is the centring underfitting for students’
microscopes.
This fitting places in the hands of
student workers a means of accurately
centring the sub-stage condenser, at a
low cost. It consists of the usual
Fig. 76.—New Centring Underfitting for underfitting tube, having a flange at the
Microscope. top which is fitted in a box between two
plates. The centring is effected by
means of two screws, which press the flange against a spring, as in the
ordinary sub-stage centring movement. The fitting can be adapted to any
form of Messrs. Watson’s and most other makers of students’ microscopes.
Watson’s Bacteriological Improved Van Heurck’s Microscope (Fig. 77) is in
every way a superior instrument, and it at once conveys a favourable
impression to the practical worker. When set up for use its many convenient
points—its excellence of workmanship and the precision of its movements—
seem to imply its special adaptation for the bacteriological laboratory and for
other high-class work where absolute reliance has to be placed in the results
obtained. Every detail of the instrument is carried out in the best possible
manner. The coarse adjustment is effected by means of a diagonal rack and
spiral pinion, which ensures the smoothest possible motion; while the fine,
the most important movement in the instrument, is made with an extra long
lever, a specialty of Messrs. Watson’s, and which imparts an extremely slow
action: this is now one of the most delicate and reliable forms of fine
adjustment. By its means the entire body is raised or lowered by means of a
milled head fixed to a screw having a hardened steel point acting on a lever
against a point attached to the body slide, in a dove-tailed fitting about 2½
inches long. Owing to the position of the controlling milled head on the
limb, it can be worked with either hand. Another feature of importance is
that, in using the fine adjustment the distance between the eye-piece and
objective remains unaltered. All the frictional parts of the microscope have
spring slots to the dove-tailed fittings, in which compensating screws are
fitted. These are some few of the more important points, to which much
thought and attention have been given. The body permits also of the use of
is the centring underfitting for students’
microscopes.
This fitting places in the hands of
student workers a means of accurately
centring the sub-stage condenser, at a
low cost. It consists of the usual
Fig. 76.—New Centring Underfitting for underfitting tube, having a flange at the
Microscope. top which is fitted in a box between two
plates. The centring is effected by
means of two screws, which press the flange against a spring, as in the
ordinary sub-stage centring movement. The fitting can be adapted to any
form of Messrs. Watson’s and most other makers of students’ microscopes.
Watson’s Bacteriological Improved Van Heurck’s Microscope (Fig. 77) is in
every way a superior instrument, and it at once conveys a favourable
impression to the practical worker. When set up for use its many convenient
points—its excellence of workmanship and the precision of its movements—
seem to imply its special adaptation for the bacteriological laboratory and for
other high-class work where absolute reliance has to be placed in the results
obtained. Every detail of the instrument is carried out in the best possible
manner. The coarse adjustment is effected by means of a diagonal rack and
spiral pinion, which ensures the smoothest possible motion; while the fine,
the most important movement in the instrument, is made with an extra long
lever, a specialty of Messrs. Watson’s, and which imparts an extremely slow
action: this is now one of the most delicate and reliable forms of fine
adjustment. By its means the entire body is raised or lowered by means of a
milled head fixed to a screw having a hardened steel point acting on a lever
against a point attached to the body slide, in a dove-tailed fitting about 2½
inches long. Owing to the position of the controlling milled head on the
limb, it can be worked with either hand. Another feature of importance is
that, in using the fine adjustment the distance between the eye-piece and
objective remains unaltered. All the frictional parts of the microscope have
spring slots to the dove-tailed fittings, in which compensating screws are
fitted. These are some few of the more important points, to which much
thought and attention have been given. The body permits also of the use of
Page 149
objectives of any other optician, since its total length when the draw tubes
are closed up is only 143 mm.; when extended, a total length of 320 mm. is
available. By this means an ample margin is left for the correction for cover-
glass thickness, whether the objective used be intended for the 160 mm. or
250 mm. tube length. The height of the microscope when placed in the
vertical position is 131⁄8 inches.
Fig. 77.—Watson’s Improved “Van Heurck Bacteriological” Microscope.
The Stage.—A somewhat new design has been used in building this up so as
to reduce vibration to a minimum. The bracket carrying the stage, instead of
being screwed on to the front of the limb, as is usually done, is made in a
solid casting, taking the sub-stage beneath, and passing into the joint at the
top of the foot. The joint bolt goes through the whole (limb and stage
are closed up is only 143 mm.; when extended, a total length of 320 mm. is
available. By this means an ample margin is left for the correction for cover-
glass thickness, whether the objective used be intended for the 160 mm. or
250 mm. tube length. The height of the microscope when placed in the
vertical position is 131⁄8 inches.
Fig. 77.—Watson’s Improved “Van Heurck Bacteriological” Microscope.
The Stage.—A somewhat new design has been used in building this up so as
to reduce vibration to a minimum. The bracket carrying the stage, instead of
being screwed on to the front of the limb, as is usually done, is made in a
solid casting, taking the sub-stage beneath, and passing into the joint at the
top of the foot. The joint bolt goes through the whole (limb and stage
Page 150
bracket), rendering the limb stage and sub-stage as firm as if it were one
piece; a point of considerable importance.
The mirrors, which are plain and concave, are mounted on a swing arm, so
that they may be turned aside when direct illumination of the object is
required. On the right hand side also there is a steel clamping bar for fixing
the microscope at any angle of inclination. The tripod foot, which has
superseded most other forms, is adopted. At the points of contact with the
table the feet are provided with cork pads, which give increased firmness
and prevent vibration to some extent.
The sub-stage is provided with a fine adjustment of similar design to that
employed for the focussing of the objective. It has become needful to
embody such a refinement, in order that sub-stage condensers of large
aperture, such as are in constant use for critical high-power work, may be
adjusted with the same facility and precision as the objective—they, in fact,
require it if the best work is to be got out of them. No pains have been spared
by Messrs. Watson to render it absolutely perfect.
Watson’s Portable Microscope.—This instrument is similar in general detail
to the Histological Microscope, but the foot, mirror stem, &c., are made to
fold up in exceedingly compact form, and when set up for use the stand is
perfectly rigid. Portable microscopes are, as a rule, but makeshifts. This,
however, is a thoroughly sound, practical instrument and capable of best
work with the highest power objectives, having good adjustments and
universal size fittings throughout, so that the objectives and apparatus made
for the larger instruments can be employed with it.
piece; a point of considerable importance.
The mirrors, which are plain and concave, are mounted on a swing arm, so
that they may be turned aside when direct illumination of the object is
required. On the right hand side also there is a steel clamping bar for fixing
the microscope at any angle of inclination. The tripod foot, which has
superseded most other forms, is adopted. At the points of contact with the
table the feet are provided with cork pads, which give increased firmness
and prevent vibration to some extent.
The sub-stage is provided with a fine adjustment of similar design to that
employed for the focussing of the objective. It has become needful to
embody such a refinement, in order that sub-stage condensers of large
aperture, such as are in constant use for critical high-power work, may be
adjusted with the same facility and precision as the objective—they, in fact,
require it if the best work is to be got out of them. No pains have been spared
by Messrs. Watson to render it absolutely perfect.
Watson’s Portable Microscope.—This instrument is similar in general detail
to the Histological Microscope, but the foot, mirror stem, &c., are made to
fold up in exceedingly compact form, and when set up for use the stand is
perfectly rigid. Portable microscopes are, as a rule, but makeshifts. This,
however, is a thoroughly sound, practical instrument and capable of best
work with the highest power objectives, having good adjustments and
universal size fittings throughout, so that the objectives and apparatus made
for the larger instruments can be employed with it.
Page 151
Fig. 78.—Watson’s Portable Microscope. Height of instrument when placed
vertically and racked down is 93⁄8 inches.
Watson’s Petrological Microscope (Fig. 79) is a modification of their
Edinburgh Students’ pattern, and designed specially for petrological and
mineralogical work.
vertically and racked down is 93⁄8 inches.
Watson’s Petrological Microscope (Fig. 79) is a modification of their
Edinburgh Students’ pattern, and designed specially for petrological and
mineralogical work.
Page 152
Fig. 79.—Students’ Petrological Microscope.
A polariscope having prisms of large size is supplied with it, the analyser
being fitted in the body, and the polariser in the under-stage fitting. The latter
has a divided circle and a spring catch at every quarter circle. By removing
the polariser and withdrawing the analyser, for which provision is made, the
microscope can be used for purposes of ordinary research. A Klein’s quartz
plate is fitted beneath the analyser, also in the body of the microscope.
The stage, which has a glass surface, rotates concentrically, and has a
divided circumferential edge reading by the verniers. The eye-piece has
cross webs to the diaphragm, and when it is desired, an analyser, having a
divided circle fitted with a calc-spar plate, can be used above the eye-piece,
and condenser lenses attached to the polariser for stereoscopic purposes. All
the fittings have the universal thread, and are interchangeable.
A polariscope having prisms of large size is supplied with it, the analyser
being fitted in the body, and the polariser in the under-stage fitting. The latter
has a divided circle and a spring catch at every quarter circle. By removing
the polariser and withdrawing the analyser, for which provision is made, the
microscope can be used for purposes of ordinary research. A Klein’s quartz
plate is fitted beneath the analyser, also in the body of the microscope.
The stage, which has a glass surface, rotates concentrically, and has a
divided circumferential edge reading by the verniers. The eye-piece has
cross webs to the diaphragm, and when it is desired, an analyser, having a
divided circle fitted with a calc-spar plate, can be used above the eye-piece,
and condenser lenses attached to the polariser for stereoscopic purposes. All
the fittings have the universal thread, and are interchangeable.
Page 153
Fig. 80.—Swift’s Histological and Physiological Microscope.
Messrs. Swift’s Microscopes.
Messrs. Swift’s Microscopes have a well-established reputation for quality
and good workmanship, and therefore can in no way suffer by comparison
when placed beside those of other opticians. One of the characteristics of
Messrs. Swift’s microscopes—and this runs through the whole series—is
that they are all made to a standard gauge, so that the several parts of the
instruments, as well as their accessories, are interchangeable; the cheaper
forms, with those of the first quality and finish. Should the student, then,
start with a No. 1 model, he can at any time build it up, as it were, with the
accessories designed for a No. 3 or 4, that is, for an instrument of double the
Messrs. Swift’s Microscopes.
Messrs. Swift’s Microscopes have a well-established reputation for quality
and good workmanship, and therefore can in no way suffer by comparison
when placed beside those of other opticians. One of the characteristics of
Messrs. Swift’s microscopes—and this runs through the whole series—is
that they are all made to a standard gauge, so that the several parts of the
instruments, as well as their accessories, are interchangeable; the cheaper
forms, with those of the first quality and finish. Should the student, then,
start with a No. 1 model, he can at any time build it up, as it were, with the
accessories designed for a No. 3 or 4, that is, for an instrument of double the
Page 154
price he started with. The optical centre is preserved throughout the whole
series of microscopes.
Fig. 81.—Swinging Leg Attachment of Swift & Son’s Four-Legged Microscope
Stand.
The tripod foot has, it appears, taken the place of some of their other forms
of instruments, while their four-legged tripod, if it can be so designated, is a
novelty of quite an unusual character.
The swing leg is attached to the framework of the tripod by the screw (Fig.
A), which is provided with a powerful steel spiral spring, compressed
between two steel collets when the screw is driven home, as shown in Fig.
B.
The expansion of this spring will obviously take up and compensate
automatically any wear and tear that is likely to occur between the bearing
surfaces, and it is therefore impossible for the fitting to get loose.
series of microscopes.
Fig. 81.—Swinging Leg Attachment of Swift & Son’s Four-Legged Microscope
Stand.
The tripod foot has, it appears, taken the place of some of their other forms
of instruments, while their four-legged tripod, if it can be so designated, is a
novelty of quite an unusual character.
The swing leg is attached to the framework of the tripod by the screw (Fig.
A), which is provided with a powerful steel spiral spring, compressed
between two steel collets when the screw is driven home, as shown in Fig.
B.
The expansion of this spring will obviously take up and compensate
automatically any wear and tear that is likely to occur between the bearing
surfaces, and it is therefore impossible for the fitting to get loose.
Page 155
Swift’s Four-legged Microscope (Fig. 80) is one possessing great stability in
whatever position it may be placed; the body being supported on a horse-
shoe platform, from which its four legs spring, the two front legs being
fixed, while the hind legs are pivoted to the platform. This arrangement of
pivoting the hind legs enables the microscope to adapt itself to any uneven
surface, thus keeping it always in a steady position, while it also reduces the
danger of being upset by any lateral movement of an accidental nature. The
feet are studded with corks, an additional aid to steadiness and fixity for
microphotography. The length of the body from the ocular to the nose-piece
is 6½ inches, and can be extended to 9 or 10 inches by means of the draw-
tube, which has a millimetre graduation. The stage, which is of horse-shoe
shape, is provided with spring clips, to which a movable mechanical stage
can at any time be attached. The sub-stage partakes of two forms, one being
an ordinary fitting, taking an ordinary condenser; the other, the regular rack
and pinion achromatic condenser with centring adjustments. It has a
diagonal rack and pinion coarse adjustment, the fine adjustment being made
by micrometer screw of the finest character.
Fig. 82.—Swift’s Spiral Rack and Pinion Coarse Adjustment.
whatever position it may be placed; the body being supported on a horse-
shoe platform, from which its four legs spring, the two front legs being
fixed, while the hind legs are pivoted to the platform. This arrangement of
pivoting the hind legs enables the microscope to adapt itself to any uneven
surface, thus keeping it always in a steady position, while it also reduces the
danger of being upset by any lateral movement of an accidental nature. The
feet are studded with corks, an additional aid to steadiness and fixity for
microphotography. The length of the body from the ocular to the nose-piece
is 6½ inches, and can be extended to 9 or 10 inches by means of the draw-
tube, which has a millimetre graduation. The stage, which is of horse-shoe
shape, is provided with spring clips, to which a movable mechanical stage
can at any time be attached. The sub-stage partakes of two forms, one being
an ordinary fitting, taking an ordinary condenser; the other, the regular rack
and pinion achromatic condenser with centring adjustments. It has a
diagonal rack and pinion coarse adjustment, the fine adjustment being made
by micrometer screw of the finest character.
Fig. 82.—Swift’s Spiral Rack and Pinion Coarse Adjustment.
Page 156
Fig. 82 is intended to illustrate the advantage of the spiral rack and pinion
which Messrs. Swift fit to their microscopes, in place of the ordinary
conventional horizontal rack and pinion movement. The advantage will at
once be seen, since there is more gearing contact between rack and pinion,
thus ensuring durability and reducing loss of time or back lash to a
minimum, with less wear and tear. The leaves of the pinion also roll into the
teeth of the rack by degrees, ensuring a very much smoother action, which, if
properly made and fitted, prevents the gearing of the two being felt by the
hand whilst focussing.
Fig. 83 is a supplementary draw-tube
with rack and pinion movement, which
can be adapted to any of Swift’s
microscopes in place of the ordinary
draw-tube, the size of the thread being
of the same diameter, so as to render
all draw-tubes, as well as other parts of
these instruments, interchangeable.
The draw-tube being divided into
millimetres can be extended from 160
to 250 millimetres. One advantage of
this arrangement is that the correct
adjustment of any objective with each
eye-piece is easily found and recorded
for future observations with the same
combination.
Messrs. Swift’s Three-legged Tripod
Microscope (Fig. 86). In most respects
the description already given of the
four-legged instrument is applicable to
this stand. Although of an apparently
Fig. 83.—Graduated Supplementary Draw-Tube. different form, it can be built up, as
already explained, into one of a higher
class. It is suitable in every way for histological investigations. The horse-
shoe platform in this, as in the preceding stand, is extremely serviceable, as
it allows the pillar of the instrument to rest firmly upon it, thus rendering the
stand very rigid.
which Messrs. Swift fit to their microscopes, in place of the ordinary
conventional horizontal rack and pinion movement. The advantage will at
once be seen, since there is more gearing contact between rack and pinion,
thus ensuring durability and reducing loss of time or back lash to a
minimum, with less wear and tear. The leaves of the pinion also roll into the
teeth of the rack by degrees, ensuring a very much smoother action, which, if
properly made and fitted, prevents the gearing of the two being felt by the
hand whilst focussing.
Fig. 83 is a supplementary draw-tube
with rack and pinion movement, which
can be adapted to any of Swift’s
microscopes in place of the ordinary
draw-tube, the size of the thread being
of the same diameter, so as to render
all draw-tubes, as well as other parts of
these instruments, interchangeable.
The draw-tube being divided into
millimetres can be extended from 160
to 250 millimetres. One advantage of
this arrangement is that the correct
adjustment of any objective with each
eye-piece is easily found and recorded
for future observations with the same
combination.
Messrs. Swift’s Three-legged Tripod
Microscope (Fig. 86). In most respects
the description already given of the
four-legged instrument is applicable to
this stand. Although of an apparently
Fig. 83.—Graduated Supplementary Draw-Tube. different form, it can be built up, as
already explained, into one of a higher
class. It is suitable in every way for histological investigations. The horse-
shoe platform in this, as in the preceding stand, is extremely serviceable, as
it allows the pillar of the instrument to rest firmly upon it, thus rendering the
stand very rigid.
Page 157
Swift’s Bacteriological Microscope (Fig. 84), designed by Professor Wright,
of the Army Medical School, Netley, a sufficient warranty of its excellency
and perfect adaptation for bacteriological high-class work. One of the
advantages connected with this microscope is the facility with which it can
be adapted for either high or low power investigation, without the necessity
of adding or detaching any part. The objectives, arranged on a triple nose-
piece, are approximately in focus when revolved into position for immediate
use, thus effecting a saving of time in changing the objective. Moreover, the
nose-piece carrying the objectives is of new construction, and fitted in such a
way that the entry of dust is rendered impossible.
Fig. 84.—Swift’s Army Bacteriological Microscope. Fig. 85. Under-Stage of same.
The Abbe condenser, fitted with an iris diaphragm, is mounted on an
eccentric arm, so that it can readily be thrown out of the axis of the
microscope when not required, without having to re-arrange the focus when
of the Army Medical School, Netley, a sufficient warranty of its excellency
and perfect adaptation for bacteriological high-class work. One of the
advantages connected with this microscope is the facility with which it can
be adapted for either high or low power investigation, without the necessity
of adding or detaching any part. The objectives, arranged on a triple nose-
piece, are approximately in focus when revolved into position for immediate
use, thus effecting a saving of time in changing the objective. Moreover, the
nose-piece carrying the objectives is of new construction, and fitted in such a
way that the entry of dust is rendered impossible.
Fig. 84.—Swift’s Army Bacteriological Microscope. Fig. 85. Under-Stage of same.
The Abbe condenser, fitted with an iris diaphragm, is mounted on an
eccentric arm, so that it can readily be thrown out of the axis of the
microscope when not required, without having to re-arrange the focus when
Page 158
again brought into position. The condenser must be turned aside when plate
cultivations and preparations of unstained bacteria are being looked over for
selection of colonies for mounting, in which case an arm carrying a quadrant
with three apertures is brought into position in place of the condenser, the
apertures being severally centred by a spring catch and used with oblique
light. This arrangement, shown in Fig. 85, is seen from the under surface of
the stage. The stage is sufficiently large, so that when Petrie plates are being
examined at the extreme edges there is little fear of their overbalancing.
Fig. 86.—Swift’s Histological Students’ Microscope.
The fine adjustment is the Swift’s Patent Campbell Differential Screw, which
offers great facilities for delicate focussing with the highest power
objectives. The stand is of the most substantial and rigid form, and thus
ensures the microscope from vibration.
cultivations and preparations of unstained bacteria are being looked over for
selection of colonies for mounting, in which case an arm carrying a quadrant
with three apertures is brought into position in place of the condenser, the
apertures being severally centred by a spring catch and used with oblique
light. This arrangement, shown in Fig. 85, is seen from the under surface of
the stage. The stage is sufficiently large, so that when Petrie plates are being
examined at the extreme edges there is little fear of their overbalancing.
Fig. 86.—Swift’s Histological Students’ Microscope.
The fine adjustment is the Swift’s Patent Campbell Differential Screw, which
offers great facilities for delicate focussing with the highest power
objectives. The stand is of the most substantial and rigid form, and thus
ensures the microscope from vibration.
Page 159
The under-stage of microscope (Fig. 85) is seen to be of the most approved
form.
Fig. 87.—Swift’s Advanced Students’ Microscope.
Swift’s Advanced Students’ Microscope.—In this microscope (Fig. 87) we
have a superior instrument for the use of the advanced student, which may
be described as of high mechanical excellence, well suited for every
requirement of work. The stand is the well-known tripod form of their
Challenger Microscope, and admits of the instrument being placed at any
angle of inclination; the body is short enough to work with objectives of
Continental makers, and is provided with a draw-tube, to elongate it to the
standard of 10 inches, with a diameter of 13⁄16 inch to take the same eye-
pieces as the larger stands. The coarse adjustment is by spiral rack and
pinion; the fine, by a carefully made differential screw motion for delicate
form.
Fig. 87.—Swift’s Advanced Students’ Microscope.
Swift’s Advanced Students’ Microscope.—In this microscope (Fig. 87) we
have a superior instrument for the use of the advanced student, which may
be described as of high mechanical excellence, well suited for every
requirement of work. The stand is the well-known tripod form of their
Challenger Microscope, and admits of the instrument being placed at any
angle of inclination; the body is short enough to work with objectives of
Continental makers, and is provided with a draw-tube, to elongate it to the
standard of 10 inches, with a diameter of 13⁄16 inch to take the same eye-
pieces as the larger stands. The coarse adjustment is by spiral rack and
pinion; the fine, by a carefully made differential screw motion for delicate
Page 160
focussing. The stage is of the horse-shoe pattern, to which a mechanical
stage can at any time be adapted, as well as an achromatic condenser to the
sub-stage seen beneath. Here the student will find the foundation for a
superior instrument.
Messrs. Baker’s Microscopes.
Of Messrs. Baker’s larger stands, the Improved “Nelson Model,” No. 2 (Fig.
88) stand is selected in preference to their more elaborate No. 1, and their
simpler form, No. 3, as a high-class instrument, and one well suited for fine
critical work; the former being somewhat better, only from having extra
adjustments; the latter possessing no superior advantage over the “Advanced
Students’” Microscope. This microscope is mounted on a solid tripod foot,
which insures stability, whether placed in a vertical, horizontal, or inclined
position; the front toes are slotted, so that they may be clamped to the base
plate of a photo-micrographic apparatus, first introduced for photo-
micrographic work, and will also be found convenient in ordinary work; as
the fine adjustment milled head is placed at the bottom of the pillar, instead
of at the top, the more usual place. For photo-micrographic work the
advantage is that the strain of the pulley in such apparatus actuates the fine
adjustment, and is less liable to cause vibration of the instrument. The
advantage when the instrument is used for ordinary work lies in the fact that
the weight of the hand is rested on the top of the tripod, thus admitting of
steadier movement of the milled head. The fine adjustment is obtained by a
“Campbell” differential screw, each revolution of which is equal to 1⁄200 m.m.
The draw-tubes being graduated in m.m., allow of either short or long tube
objectives being used, closing up to 150 m.m. and extending to 280 m.m.,
the rack and pinion adjustment to the lower tube affording a ready means of
correction for cover-glass thicknesses. The eye-piece gauge, as will be seen
from its dimensions, is of large size, being the same as that adopted by Zeiss
for his long tube compensating oculars; smaller eye-pieces can, however, be
adapted at any time.
stage can at any time be adapted, as well as an achromatic condenser to the
sub-stage seen beneath. Here the student will find the foundation for a
superior instrument.
Messrs. Baker’s Microscopes.
Of Messrs. Baker’s larger stands, the Improved “Nelson Model,” No. 2 (Fig.
88) stand is selected in preference to their more elaborate No. 1, and their
simpler form, No. 3, as a high-class instrument, and one well suited for fine
critical work; the former being somewhat better, only from having extra
adjustments; the latter possessing no superior advantage over the “Advanced
Students’” Microscope. This microscope is mounted on a solid tripod foot,
which insures stability, whether placed in a vertical, horizontal, or inclined
position; the front toes are slotted, so that they may be clamped to the base
plate of a photo-micrographic apparatus, first introduced for photo-
micrographic work, and will also be found convenient in ordinary work; as
the fine adjustment milled head is placed at the bottom of the pillar, instead
of at the top, the more usual place. For photo-micrographic work the
advantage is that the strain of the pulley in such apparatus actuates the fine
adjustment, and is less liable to cause vibration of the instrument. The
advantage when the instrument is used for ordinary work lies in the fact that
the weight of the hand is rested on the top of the tripod, thus admitting of
steadier movement of the milled head. The fine adjustment is obtained by a
“Campbell” differential screw, each revolution of which is equal to 1⁄200 m.m.
The draw-tubes being graduated in m.m., allow of either short or long tube
objectives being used, closing up to 150 m.m. and extending to 280 m.m.,
the rack and pinion adjustment to the lower tube affording a ready means of
correction for cover-glass thicknesses. The eye-piece gauge, as will be seen
from its dimensions, is of large size, being the same as that adopted by Zeiss
for his long tube compensating oculars; smaller eye-pieces can, however, be
adapted at any time.
Page 161
Fig. 88.—Baker’s Improved “Nelson Model” Microscope. Dimensions.—Height
when in vertical position and body racked down, 11′′; Height of stage, 41⁄8′′;
Height of optic axis when in horizontal position, 8½′′; Spread of tripod foot, 8 ×
8½′′; Diameter of mirrors, 23⁄8′′; Internal diameter of draw-tube, 13⁄10′′.
The mechanical rotating stage is divided on brass to 1⁄100 inch, with clamping
bars and stop, by which a specimen can always be brought back to a certain
position for registration. The sub-stage has rack-work focussing adjustment,
and centring screws; a fine adjustment is added, if desired. On the whole, the
instrument is suitable for special critical work, and is equally well suited for
photo-micrography.
when in vertical position and body racked down, 11′′; Height of stage, 41⁄8′′;
Height of optic axis when in horizontal position, 8½′′; Spread of tripod foot, 8 ×
8½′′; Diameter of mirrors, 23⁄8′′; Internal diameter of draw-tube, 13⁄10′′.
The mechanical rotating stage is divided on brass to 1⁄100 inch, with clamping
bars and stop, by which a specimen can always be brought back to a certain
position for registration. The sub-stage has rack-work focussing adjustment,
and centring screws; a fine adjustment is added, if desired. On the whole, the
instrument is suitable for special critical work, and is equally well suited for
photo-micrography.
Page 162
Fig. 89.—Baker’s Advanced Students’ Microscope. Dimensions.—Height when in
vertical position and body racked down, 11¼′′; Height of stage, 4¾′′; Width of
stage, 4′′; Height of optic axis when in horizontal position, 6½′′; Spread of foot, 6′′
× 6′′; Diameter of mirrors, 1¾′′; Internal diameter of draw-tube, 11⁄12′′.
Explanatory lettering of instrument: A, Huyghenian eye-piece; B, draw-tube
graduated in millimetres; C, nose-piece; D, coarse adjustment; E, fine adjustment
with millimetre screw; F, horse-shoe sliding stage, graduated with sliding bar in
vertical and horizontal directions for use as finder; G, sub-stage rack and pinion
screw; H and I, centring screws to sub-stage; J, carrier for condenser; K, mirror
with movable arm supported on solid tripod foot.
The points of difference between this stand and the No. 1 model are that in
the latter the fine adjustment carries the body only, and not the rack
adjustment; the limb carrying both the body and the sub-stage is in one
piece, giving, if possible, still greater rigidity; the rotation of the mechanical
stage, which is divided on silver, is complete, and can be actuated by hand or
rack work; it has a clamping screw and fine adjustment to sub-stage.
vertical position and body racked down, 11¼′′; Height of stage, 4¾′′; Width of
stage, 4′′; Height of optic axis when in horizontal position, 6½′′; Spread of foot, 6′′
× 6′′; Diameter of mirrors, 1¾′′; Internal diameter of draw-tube, 11⁄12′′.
Explanatory lettering of instrument: A, Huyghenian eye-piece; B, draw-tube
graduated in millimetres; C, nose-piece; D, coarse adjustment; E, fine adjustment
with millimetre screw; F, horse-shoe sliding stage, graduated with sliding bar in
vertical and horizontal directions for use as finder; G, sub-stage rack and pinion
screw; H and I, centring screws to sub-stage; J, carrier for condenser; K, mirror
with movable arm supported on solid tripod foot.
The points of difference between this stand and the No. 1 model are that in
the latter the fine adjustment carries the body only, and not the rack
adjustment; the limb carrying both the body and the sub-stage is in one
piece, giving, if possible, still greater rigidity; the rotation of the mechanical
stage, which is divided on silver, is complete, and can be actuated by hand or
rack work; it has a clamping screw and fine adjustment to sub-stage.
Page 163
Baker’s Advanced Students’ Microscope (Fig. 89) may be described as a
typical instrument, equally suitable for histological work and that of the
advanced student. The intention of the maker in simplifying the adjustments
and reducing the instrument in size, was to furnish a well-finished portable
instrument at a moderate cost. This object has not been attained by supplying
adjustments of second-rate quality, but by reducing their number to a
minimum.
Fig. 90.—The Mayall Removable Mechanical Stage.
The tripod foot of the “Nelson Model” is replaced by a claw foot, which is in
effect a tripod, as it rests on three points; it has not the same wide spread, but
this, far from being a disadvantage, renders the instrument more portable. It
has rack and pinion coarse and Campbell differential screw fine adjustments,
draw-tube graduated in m.m., extending to 180 m.m., eye-piece gauge the
same as the Continental size, large square open stage to afford the greater
freedom of manipulation; sliding bar with graduations on bar and stage,
typical instrument, equally suitable for histological work and that of the
advanced student. The intention of the maker in simplifying the adjustments
and reducing the instrument in size, was to furnish a well-finished portable
instrument at a moderate cost. This object has not been attained by supplying
adjustments of second-rate quality, but by reducing their number to a
minimum.
Fig. 90.—The Mayall Removable Mechanical Stage.
The tripod foot of the “Nelson Model” is replaced by a claw foot, which is in
effect a tripod, as it rests on three points; it has not the same wide spread, but
this, far from being a disadvantage, renders the instrument more portable. It
has rack and pinion coarse and Campbell differential screw fine adjustments,
draw-tube graduated in m.m., extending to 180 m.m., eye-piece gauge the
same as the Continental size, large square open stage to afford the greater
freedom of manipulation; sliding bar with graduations on bar and stage,
Page 164
which suffice for registering any given field under a low power; holes are
also drilled in the stage ready to receive an attachable mechanical stage
should it be thought advisable to add one at a later date. The sub-stage is of
the universal size with rack-work focussing, adjustment, and centring
screws.
Fig. 91.—Baker’s Model Histological Microscope. Dimensions.—Height when in
vertical position and body racked down, 10½′′; Height of stage, 4′′; Width of stage,
3½′′; Height of optic axis when in horizontal position, 5¼′′; Spread of foot, 5¼′′;
Diameter of mirrors, 15⁄8′′; Internal diameter of draw-tube, 11⁄12′′.
Messrs. Baker have recently introduced a similar instrument with swing-out
sub-stage and adjustments for compensating for wear and tear of rack. The
stage is also somewhat larger from back to front.
also drilled in the stage ready to receive an attachable mechanical stage
should it be thought advisable to add one at a later date. The sub-stage is of
the universal size with rack-work focussing, adjustment, and centring
screws.
Fig. 91.—Baker’s Model Histological Microscope. Dimensions.—Height when in
vertical position and body racked down, 10½′′; Height of stage, 4′′; Width of stage,
3½′′; Height of optic axis when in horizontal position, 5¼′′; Spread of foot, 5¼′′;
Diameter of mirrors, 15⁄8′′; Internal diameter of draw-tube, 11⁄12′′.
Messrs. Baker have recently introduced a similar instrument with swing-out
sub-stage and adjustments for compensating for wear and tear of rack. The
stage is also somewhat larger from back to front.
Page 165
These stands are very suitable for bacteriological research, and for amateurs
wishing to obtain a stand which will carry all the apparatus they are likely to
need, without going to the expense of the larger models, no better instrument
could be desired.
Their “Removable Mechanical Stage” (Fig. 90) is a modification of the
pattern designed by the late Mr. J. Mayall. The vertical movement is by rack
and pinion, giving a range of 11⁄8 inch. The horizontal motion of 1½ inch is
accomplished by means of a quick-acting screw. The object is pressed tightly
to the stage of the microscope by means of three points, and the whole of the
mechanical part is firmly clamped by two thumb screws which can be
readily removed. The stage is made to carry slides of any size less than 1¾
inch wide.
Baker’s Histological Microscope (Fig. 91) is of a different type to the
preceding, and is intended to represent one of medium power, affording
magnification of about × 400 as a maximum. It is supplied with a diaphragm
beneath the stage, without other illuminating apparatus than that of the
mirror. But if the adjustments of such a stand are good, there is no reason
why some form of sub-stage condenser should not be added, to make the
instrument somewhat more serviceable. There is, however, a rather too
limited space beneath the stage of an instrument of this kind to admit of a
sub-stage condenser, consequently it cannot be said to be suitable for critical
work. For all ordinary students’ work this microscope is certainly available.
wishing to obtain a stand which will carry all the apparatus they are likely to
need, without going to the expense of the larger models, no better instrument
could be desired.
Their “Removable Mechanical Stage” (Fig. 90) is a modification of the
pattern designed by the late Mr. J. Mayall. The vertical movement is by rack
and pinion, giving a range of 11⁄8 inch. The horizontal motion of 1½ inch is
accomplished by means of a quick-acting screw. The object is pressed tightly
to the stage of the microscope by means of three points, and the whole of the
mechanical part is firmly clamped by two thumb screws which can be
readily removed. The stage is made to carry slides of any size less than 1¾
inch wide.
Baker’s Histological Microscope (Fig. 91) is of a different type to the
preceding, and is intended to represent one of medium power, affording
magnification of about × 400 as a maximum. It is supplied with a diaphragm
beneath the stage, without other illuminating apparatus than that of the
mirror. But if the adjustments of such a stand are good, there is no reason
why some form of sub-stage condenser should not be added, to make the
instrument somewhat more serviceable. There is, however, a rather too
limited space beneath the stage of an instrument of this kind to admit of a
sub-stage condenser, consequently it cannot be said to be suitable for critical
work. For all ordinary students’ work this microscope is certainly available.
Page 166
Fig. 92.—Rousselet’s Tank Microscope.
The stand of the Model Histological Microscope has the same form of foot
as the more advanced student’s stand. It is somewhat lighter, and more
portable, a matter of consideration in a student’s microscope, which often
has to be carried to and from a class-room. It is provided with rack and
pinion coarse adjustment, and a Campbell differential screw fine adjustment,
draw-tube, and diaphragm; the diaphragm carrier being of the universal size,
so that it can be replaced by an Abbe condenser at any time. With the
additions suggested, this instrument can be made equal to those of a higher
standard.
Rousselet’s Tank Microscope (Fig. 92), for rapidly looking over pond water
and weeds, consists of a jointed arm moving parallel to the side of the tank
to carry an aplanatic lens; the arm is focussed by means of rack and pinion
fixed to the upright of a mahogany stand, upon which the tank can be placed,
or it can be clamped directly to the tank by means of a screw. This handy
form of pond microscope is made by Messrs. Baker.
The stand of the Model Histological Microscope has the same form of foot
as the more advanced student’s stand. It is somewhat lighter, and more
portable, a matter of consideration in a student’s microscope, which often
has to be carried to and from a class-room. It is provided with rack and
pinion coarse adjustment, and a Campbell differential screw fine adjustment,
draw-tube, and diaphragm; the diaphragm carrier being of the universal size,
so that it can be replaced by an Abbe condenser at any time. With the
additions suggested, this instrument can be made equal to those of a higher
standard.
Rousselet’s Tank Microscope (Fig. 92), for rapidly looking over pond water
and weeds, consists of a jointed arm moving parallel to the side of the tank
to carry an aplanatic lens; the arm is focussed by means of rack and pinion
fixed to the upright of a mahogany stand, upon which the tank can be placed,
or it can be clamped directly to the tank by means of a screw. This handy
form of pond microscope is made by Messrs. Baker.
Page 167
Pillischer’s Microscopes.
Mr. Pillischer (New Bond Street) is favourably known for the excellency of
his instruments. He has lately brought out several microscopes of an
improved form. His larger model, the “New International,” consists of a
solid, well-built, firm tripod stand of the Ross-Jackson pattern, which
appears to be quite in the ascendant among London opticians; rack and
pinion coarse adjustment, and a superior micrometer fine adjustment; sub-
stage with centring screws and rack and pinion focussing adjustment; a new
form of sliding pin-hole diaphragm and iris diaphragm; B and C eye-pieces;
5⁄8 and 1⁄7 objectives; Abbe condenser, N.A. 1·20; in every respect a perfect
model, neatly packed in a mahogany case, for a very moderate sum. Mr.
Pillischer’s No. 2 (Fig. 93) “International” Microscope, being the Army
pattern as well as the student’s, is well adapted for clinical work. A firm
tripod stand supports two dark bronze uprights, with rack and pinion coarse
adjustment, e, and fine adjustment, d, the stage, i, is wide and suitable for
clinical work, and large enough for dissecting upon. The whole instrument is
well made; the coarse adjustment is so good that the one-eighth inch can be
focussed with ease, and without using the fine adjustment.
For a few shillings extra, a mechanical stage can be added, consisting of
levers, having an action similar to the movements of a parallel ruler, which is
so easy of adjustment that it can be worked under the eighth-inch objective
with the hands—an advantage in a clinical microscope.
Mr. Pillischer (New Bond Street) is favourably known for the excellency of
his instruments. He has lately brought out several microscopes of an
improved form. His larger model, the “New International,” consists of a
solid, well-built, firm tripod stand of the Ross-Jackson pattern, which
appears to be quite in the ascendant among London opticians; rack and
pinion coarse adjustment, and a superior micrometer fine adjustment; sub-
stage with centring screws and rack and pinion focussing adjustment; a new
form of sliding pin-hole diaphragm and iris diaphragm; B and C eye-pieces;
5⁄8 and 1⁄7 objectives; Abbe condenser, N.A. 1·20; in every respect a perfect
model, neatly packed in a mahogany case, for a very moderate sum. Mr.
Pillischer’s No. 2 (Fig. 93) “International” Microscope, being the Army
pattern as well as the student’s, is well adapted for clinical work. A firm
tripod stand supports two dark bronze uprights, with rack and pinion coarse
adjustment, e, and fine adjustment, d, the stage, i, is wide and suitable for
clinical work, and large enough for dissecting upon. The whole instrument is
well made; the coarse adjustment is so good that the one-eighth inch can be
focussed with ease, and without using the fine adjustment.
For a few shillings extra, a mechanical stage can be added, consisting of
levers, having an action similar to the movements of a parallel ruler, which is
so easy of adjustment that it can be worked under the eighth-inch objective
with the hands—an advantage in a clinical microscope.
Page 168
Fig. 93.—Pillischer’s “International” Microscope.
The following reference letters serve to explain the general construction of
the microscope (Fig. 93):—a, the eye-piece; b, the draw-tube; c, the sliding-
tube; d, micrometer or fine adjustment; e e, the coarse adjustment; g, the
mirror arm and mirror; h, sub-stage carrying Abbe condenser; i, the stage
with spring-clips; j, objectives screwed into place and double nose-piece.
The “Kosmos” is Pillischer’s cheaper model. The stand of this somewhat
novel and original microscope is framed entirely of brass and gun-metal. The
fine adjustment is very sensitive and perfectly steady, admitting of the
highest immersion objectives being used. The optical parts are constructed
upon principles consistent with the latest improvements. It has a claw-foot
stand with a semi-circular arm, which carries the body, with sliding-tube
coarse adjustment, and micrometer screw fine adjustment, with a large
The following reference letters serve to explain the general construction of
the microscope (Fig. 93):—a, the eye-piece; b, the draw-tube; c, the sliding-
tube; d, micrometer or fine adjustment; e e, the coarse adjustment; g, the
mirror arm and mirror; h, sub-stage carrying Abbe condenser; i, the stage
with spring-clips; j, objectives screwed into place and double nose-piece.
The “Kosmos” is Pillischer’s cheaper model. The stand of this somewhat
novel and original microscope is framed entirely of brass and gun-metal. The
fine adjustment is very sensitive and perfectly steady, admitting of the
highest immersion objectives being used. The optical parts are constructed
upon principles consistent with the latest improvements. It has a claw-foot
stand with a semi-circular arm, which carries the body, with sliding-tube
coarse adjustment, and micrometer screw fine adjustment, with a large
Page 169
square stage diaphragm and mirror. The instrument is neatly packed in a
mahogany box, together with the A or B eye-piece, 1-inch and 1⁄5-inch
objectives of good defining and penetrating power, magnifying from 30 to
380 diameters, in mahogany cabinet, for the moderate sum of £5.
Pillischer’s Binocular Microscope (Fig. 94) is constructed on a plan
somewhat intermediate between that of Beck’s and Ross’s well-known
patterns, and in point of finish is equal to any student’s microscope in use.
The semi-circular form given to the arm carrying the body increases the
strength and solidity of the instrument, although it is doubtful whether it
adds to its steadiness when placed in the horizontal position. The straight
body rests for a great part of its length upon a parallel bar of solid brass
ploughed into which is a groove for the reception of the rack attached to the
body, the groove being of such a form that the rack is held firmly while the
pinion glides smoothly through it. A steady, uniform motion is thus obtained,
which almost renders the fine adjustment unnecessary. The binocular bodies
are inclined at a smaller angle to one another than in most instruments;
nevertheless, the range of motion given to the eye-pieces by the rack and
pinion enables those whose eyes are widely separated to use the instrument
with comfort. The prism is so well set that it illuminates both fields with
equal intensity. The stage is provided with rectangular traversing movements
to the extent of an inch and a quarter in each direction. The milled heads
which effect these are placed on the same axis, instead of side by side, one
of them—the vertical one—being repeated on the left of the stage, so that the
movements may be communicated either by the right hand alone or by both
hands acting in concert. The stage-plate has the ordinary vertical and
rotatory motions, but to a much greater extent than usual; and the platform
which carries the object is provided with a spring clip to secure the object
when the stage is placed in the vertical position. A new form of sub-stage
with centring screws is made to carry the Abbe achromatic condenser,
diaphragm, polarising and other apparatus.
mahogany box, together with the A or B eye-piece, 1-inch and 1⁄5-inch
objectives of good defining and penetrating power, magnifying from 30 to
380 diameters, in mahogany cabinet, for the moderate sum of £5.
Pillischer’s Binocular Microscope (Fig. 94) is constructed on a plan
somewhat intermediate between that of Beck’s and Ross’s well-known
patterns, and in point of finish is equal to any student’s microscope in use.
The semi-circular form given to the arm carrying the body increases the
strength and solidity of the instrument, although it is doubtful whether it
adds to its steadiness when placed in the horizontal position. The straight
body rests for a great part of its length upon a parallel bar of solid brass
ploughed into which is a groove for the reception of the rack attached to the
body, the groove being of such a form that the rack is held firmly while the
pinion glides smoothly through it. A steady, uniform motion is thus obtained,
which almost renders the fine adjustment unnecessary. The binocular bodies
are inclined at a smaller angle to one another than in most instruments;
nevertheless, the range of motion given to the eye-pieces by the rack and
pinion enables those whose eyes are widely separated to use the instrument
with comfort. The prism is so well set that it illuminates both fields with
equal intensity. The stage is provided with rectangular traversing movements
to the extent of an inch and a quarter in each direction. The milled heads
which effect these are placed on the same axis, instead of side by side, one
of them—the vertical one—being repeated on the left of the stage, so that the
movements may be communicated either by the right hand alone or by both
hands acting in concert. The stage-plate has the ordinary vertical and
rotatory motions, but to a much greater extent than usual; and the platform
which carries the object is provided with a spring clip to secure the object
when the stage is placed in the vertical position. A new form of sub-stage
with centring screws is made to carry the Abbe achromatic condenser,
diaphragm, polarising and other apparatus.
Page 170
Fig. 94.—Pillischer’s Binocular Microscope.
Continental Microscopes.
Continental Microscopes.—The better known among continental opticians
are Zeiss, Leitz, Seibert, Reichert and Hartnack. All seem to have vied with
each other in the attainment of perfection in the manufacture of the most
useful forms of microscopes. The late Carl Zeiss did more for the modern
microscope than either of the opticians referred to above. I therefore take a
medium typical model of his from a long series of highly-finished
instruments for my illustration. Zeiss’s successors have of late endeavoured
to perfect the mechanical details of their instruments in three or four
directions, i.e., fundamental features of the stand, stage arrangements, means
of focussing, and illumination.
Continental Microscopes.
Continental Microscopes.—The better known among continental opticians
are Zeiss, Leitz, Seibert, Reichert and Hartnack. All seem to have vied with
each other in the attainment of perfection in the manufacture of the most
useful forms of microscopes. The late Carl Zeiss did more for the modern
microscope than either of the opticians referred to above. I therefore take a
medium typical model of his from a long series of highly-finished
instruments for my illustration. Zeiss’s successors have of late endeavoured
to perfect the mechanical details of their instruments in three or four
directions, i.e., fundamental features of the stand, stage arrangements, means
of focussing, and illumination.
Page 171
The Stand.—The general form of the stand still partakes too much of the
original sameness of type introduced by Oberhäuser, and modified and
improved by Hartnack; the “Babuchin” stand being still in favour with some
few makers. The greater firmness and steadiness of Zeiss’s stand (Fig. 95) is
secured by the horse-shoe form of foot, which, for the most part, is massive
and well adapted to carry the stout uprights, which support a well-balanced,
substantial body-tube and a graduated draw-tube, circular stage with a
vulcanite disc, 4 inches in diameter; a sub-stage with centring arrangement
for Abbe’s illuminating apparatus, and iris diaphragm and other diaphragms
for use when the condenser is thrown aside. The mirror is full-sized, plane
and concave. The coarse adjustment is regulated by a rack and pillion
movement so perfect that objectives of medium power can be focussed by it
alone. The fine adjustment is made by micrometer screw, the force exercised
by which is transferred to the movable body by a single contact between two
hardened steel surfaces. This ensures extremely delicate and uniform motion
of the body which carries the tube.
The divisions in the milled head of the screw furnish a means for the
registration of the vertical movements of the tube. In the latest stands, each
division corresponds to an elevation or depression of the tube in the direction
of the optic axis of 0·01 mm. By this means measurements of thicknesses
may be made with a considerable degree of accuracy, the upper and lower
surfaces of the object being successively focussed, and the amount read off
on the milled-head, by the fixed index. In doing this, care must be taken to
make both adjustments by a rotation of the screw in the same direction. The
thickness of an object in air is then equal to the difference between the two
readings. By this means the thickness of any other substance may be
measured—that, for instance, of the cover-glass of the object.
original sameness of type introduced by Oberhäuser, and modified and
improved by Hartnack; the “Babuchin” stand being still in favour with some
few makers. The greater firmness and steadiness of Zeiss’s stand (Fig. 95) is
secured by the horse-shoe form of foot, which, for the most part, is massive
and well adapted to carry the stout uprights, which support a well-balanced,
substantial body-tube and a graduated draw-tube, circular stage with a
vulcanite disc, 4 inches in diameter; a sub-stage with centring arrangement
for Abbe’s illuminating apparatus, and iris diaphragm and other diaphragms
for use when the condenser is thrown aside. The mirror is full-sized, plane
and concave. The coarse adjustment is regulated by a rack and pillion
movement so perfect that objectives of medium power can be focussed by it
alone. The fine adjustment is made by micrometer screw, the force exercised
by which is transferred to the movable body by a single contact between two
hardened steel surfaces. This ensures extremely delicate and uniform motion
of the body which carries the tube.
The divisions in the milled head of the screw furnish a means for the
registration of the vertical movements of the tube. In the latest stands, each
division corresponds to an elevation or depression of the tube in the direction
of the optic axis of 0·01 mm. By this means measurements of thicknesses
may be made with a considerable degree of accuracy, the upper and lower
surfaces of the object being successively focussed, and the amount read off
on the milled-head, by the fixed index. In doing this, care must be taken to
make both adjustments by a rotation of the screw in the same direction. The
thickness of an object in air is then equal to the difference between the two
readings. By this means the thickness of any other substance may be
measured—that, for instance, of the cover-glass of the object.
Page 172
Fig. 95.—Zeiss’s Medium Stand Microscope.
The medium tube-length of the microscope is 160 mm. from the attachment
of the objective to the eye-piece end. The draw-tube admits of the length
being increased or diminished, and this may be read off by means of the
millimetre scale engraved on the tube. My description of this model also
applies to the higher class microscopes, which will be found in every way
well finished and adapted to biological and scientific research.
E. Leitz’s of Wetzlar Microscopes.—This optician publishes a series of
twelve high-class forms of instruments. By preference, the horse-shoe form
of stand (Fig. 96) is adopted in the whole of this maker’s models, the body
being supported on a hinge joint and clamped over, and fitted with a circular
revolving centred mechanical stage, attached to the ordinary stage by means
of a set pin, which fixes the stage in position. By removing the screw, the
The medium tube-length of the microscope is 160 mm. from the attachment
of the objective to the eye-piece end. The draw-tube admits of the length
being increased or diminished, and this may be read off by means of the
millimetre scale engraved on the tube. My description of this model also
applies to the higher class microscopes, which will be found in every way
well finished and adapted to biological and scientific research.
E. Leitz’s of Wetzlar Microscopes.—This optician publishes a series of
twelve high-class forms of instruments. By preference, the horse-shoe form
of stand (Fig. 96) is adopted in the whole of this maker’s models, the body
being supported on a hinge joint and clamped over, and fitted with a circular
revolving centred mechanical stage, attached to the ordinary stage by means
of a set pin, which fixes the stage in position. By removing the screw, the
Page 173
stage can be detached; in this way, the
stage serves for searching over large
surfaces and registering the results.
Fig. 96.—E. Leitz’s Medium-sized
Microscope.
Fig. 97.—Leitz’s Dissecting Microscope.
The coarse adjustment is made by rack and pinion, and the fine adjustment
by micrometer screw, the head of which is provided with a scale reading 1⁄100
mm. The draw-tube is also cut and ruled to millimetre scale. The sub-stage
has rack and pinion movement, and is arranged for the Abbe condenser and
iris diaphragm. This is attached to the upper stage by means of a set pin,
stage serves for searching over large
surfaces and registering the results.
Fig. 96.—E. Leitz’s Medium-sized
Microscope.
Fig. 97.—Leitz’s Dissecting Microscope.
The coarse adjustment is made by rack and pinion, and the fine adjustment
by micrometer screw, the head of which is provided with a scale reading 1⁄100
mm. The draw-tube is also cut and ruled to millimetre scale. The sub-stage
has rack and pinion movement, and is arranged for the Abbe condenser and
iris diaphragm. This is attached to the upper stage by means of a set pin,
Page 174
which fixes and retains it in position after perfect centring. By removing the
pin, the sub-stage can be either detached or swung aside by pressing a
button. In short, this microscope is in all respects well furnished and fitted
with the requisite complex mechanism necessitated by modern high-class
technicological work.
Leitz’s students’ microscope, with sliding body, micrometer screw fine
adjustment, concave mirror, two eye-pieces and two objectives, ¾ inch and
1⁄8 inch, in mahogany case, costs £3 10s. Leitz’s dissecting microscope, with
a heavy foot and rests, is fitted with two aplanatic lenses, magnifying × 10, ×
20 diameters.
Reichert and Seibert adhere to the same model as that of Zeiss, and therefore
require only a brief notice. Their microscopes are characterised by
substantial workmanship, suitable construction, and exact centring. The
coarse adjustment is obtained in the usual way by rack and pinion, the fine
by micrometer screws, which work easily, and are protected against wear
and tear by having their working surfaces hardened. The stands of the better
class instruments have micrometer screws graduated, and draw-tubes cut to
millimetre scale. Their mechanical stages and sub-stages and accessories are
in every way well finished; stage forceps, tests, and an assortment of cover
glasses and slides being added. Their first-class microscopes are sent out in
mahogany boxes.
On going through the continental makers’ catalogues, it will be noticed that
their well-equipped microscopes are rather more costly than that of their
English confreres. It is understood Messrs. Baker and Watson are the
constituted agents for these opticians.
Nachet’s Microscope, a new form of which was first seen at the Antwerp
Exhibition 1892, is very solidly built, and has all the qualities necessary for
histological work. The stage rotates about the optic axis, and carries a
movable slide holder. The coarse adjustment is by rack and pinion
movement, the fine by the new system of micrometer screw (described in the
journal of the Royal Microscopical Society of 1886), with divided head
indicating the 1⁄400 part of a mm. The plane and convex mirror is mounted on
a jointed arm. The draw-tube is divided into millimetres. The illuminating
system, consisting of a wide-angled Abbe condenser (N.A. 1·40) with iris
pin, the sub-stage can be either detached or swung aside by pressing a
button. In short, this microscope is in all respects well furnished and fitted
with the requisite complex mechanism necessitated by modern high-class
technicological work.
Leitz’s students’ microscope, with sliding body, micrometer screw fine
adjustment, concave mirror, two eye-pieces and two objectives, ¾ inch and
1⁄8 inch, in mahogany case, costs £3 10s. Leitz’s dissecting microscope, with
a heavy foot and rests, is fitted with two aplanatic lenses, magnifying × 10, ×
20 diameters.
Reichert and Seibert adhere to the same model as that of Zeiss, and therefore
require only a brief notice. Their microscopes are characterised by
substantial workmanship, suitable construction, and exact centring. The
coarse adjustment is obtained in the usual way by rack and pinion, the fine
by micrometer screws, which work easily, and are protected against wear
and tear by having their working surfaces hardened. The stands of the better
class instruments have micrometer screws graduated, and draw-tubes cut to
millimetre scale. Their mechanical stages and sub-stages and accessories are
in every way well finished; stage forceps, tests, and an assortment of cover
glasses and slides being added. Their first-class microscopes are sent out in
mahogany boxes.
On going through the continental makers’ catalogues, it will be noticed that
their well-equipped microscopes are rather more costly than that of their
English confreres. It is understood Messrs. Baker and Watson are the
constituted agents for these opticians.
Nachet’s Microscope, a new form of which was first seen at the Antwerp
Exhibition 1892, is very solidly built, and has all the qualities necessary for
histological work. The stage rotates about the optic axis, and carries a
movable slide holder. The coarse adjustment is by rack and pinion
movement, the fine by the new system of micrometer screw (described in the
journal of the Royal Microscopical Society of 1886), with divided head
indicating the 1⁄400 part of a mm. The plane and convex mirror is mounted on
a jointed arm. The draw-tube is divided into millimetres. The illuminating
system, consisting of a wide-angled Abbe condenser (N.A. 1·40) with iris
Page 175
diaphragm, is raised or lowered by rack and pinion screws. The iris
diaphragm, being mounted on a wheel, is worked by a tangent screw, which
by a very slight movement causes the aperture of the diaphragm to pass from
the centre to the periphery of the condenser. Altogether the arrangement of
the sub-stage is novel, and the instrument is extremely well arranged and
adapted to modern requirements.
Nachet and Hartnack, of Paris, hold an almost equal rank as makers of first-
class microscopes, and in point of excellence of workmanship fairy rival
those of our English makers.
Fig. 98.—Nachet’s Class Demonstrating Microscope.
There are very many other London and Continental makers of microscopes
besides those especially mentioned, who have well-sustained reputations as
opticians, and who, from want of space, I have been obliged to pass over.
Messrs. Newton’s Students’ Microscope must be mentioned with respect. It
is a good and useful instrument, has a firm stand with a reversible (rotatory)
body movement, which seems to ensure steadiness when brought into the
horizontal position for micro-photographic purposes. There are other
opticians whose microscopes have stood the test of time—Messrs. Collins,
Crouch, &c. It may, however, be taken as a well-established fact that those
opticians known to manufacture the more highly-finished models also
diaphragm, being mounted on a wheel, is worked by a tangent screw, which
by a very slight movement causes the aperture of the diaphragm to pass from
the centre to the periphery of the condenser. Altogether the arrangement of
the sub-stage is novel, and the instrument is extremely well arranged and
adapted to modern requirements.
Nachet and Hartnack, of Paris, hold an almost equal rank as makers of first-
class microscopes, and in point of excellence of workmanship fairy rival
those of our English makers.
Fig. 98.—Nachet’s Class Demonstrating Microscope.
There are very many other London and Continental makers of microscopes
besides those especially mentioned, who have well-sustained reputations as
opticians, and who, from want of space, I have been obliged to pass over.
Messrs. Newton’s Students’ Microscope must be mentioned with respect. It
is a good and useful instrument, has a firm stand with a reversible (rotatory)
body movement, which seems to ensure steadiness when brought into the
horizontal position for micro-photographic purposes. There are other
opticians whose microscopes have stood the test of time—Messrs. Collins,
Crouch, &c. It may, however, be taken as a well-established fact that those
opticians known to manufacture the more highly-finished models also
Page 176
produce the more serviceable forms of students’ class-room, and other
microscopes.
The Bacteriological Microscope.
The microscope required for bacteriological studies should be perfect in all
its parts. With regard to the choice of an instrument, it is very much a matter
of price, since the most perfect is usually the most costly; I shall therefore
proceed to give a typical example of the instrument in use in a
bacteriological laboratory. The microscope should possess the following
qualifications, all of which are absolutely necessary for the study of such
minute objects as bacteria and other micro-organisms.
“The typical bacteriological microscope should be well equipped with
objectives of sufficiently high magnifying power, and with a special form of
illuminating apparatus; while the mechanical arrangements for focussing
should act with the greatest smoothness and precision; the stage, also, should
be wide enough to admit of the examination of plate cultivations.”
We will consider these several points and recommendations seriatim,
commencing with the stand.
Messrs. Watson & Sons’ Van Heurck model stand so well answers the
several conditions laid down by an experienced teacher of bacteriology, that
I have no hesitation in presenting it to my readers as a typical instrument,
one in every way worthy of the high praise it has already received from
those who have worked with it, and whose judgment may be relied upon in
every way. The microscope is fully described among Messrs. Watson’s
instruments, page 108.
The Stand.—A good firm stand is undoubtedly of the first importance for all
high-class work. The steadiness of the instrument and its entire freedom
from vibration depends largely upon the form of the stand. I am glad to find
Dr. Crookshank in accord with me as to the Ross-Jackson model, one which,
in my opinion, has not been entirely superseded by models of a more recent
date. Indeed, the latest improvement effected in the Ross-Jackson form, in
which attention has been given to the spreading-out of the feet, has
microscopes.
The Bacteriological Microscope.
The microscope required for bacteriological studies should be perfect in all
its parts. With regard to the choice of an instrument, it is very much a matter
of price, since the most perfect is usually the most costly; I shall therefore
proceed to give a typical example of the instrument in use in a
bacteriological laboratory. The microscope should possess the following
qualifications, all of which are absolutely necessary for the study of such
minute objects as bacteria and other micro-organisms.
“The typical bacteriological microscope should be well equipped with
objectives of sufficiently high magnifying power, and with a special form of
illuminating apparatus; while the mechanical arrangements for focussing
should act with the greatest smoothness and precision; the stage, also, should
be wide enough to admit of the examination of plate cultivations.”
We will consider these several points and recommendations seriatim,
commencing with the stand.
Messrs. Watson & Sons’ Van Heurck model stand so well answers the
several conditions laid down by an experienced teacher of bacteriology, that
I have no hesitation in presenting it to my readers as a typical instrument,
one in every way worthy of the high praise it has already received from
those who have worked with it, and whose judgment may be relied upon in
every way. The microscope is fully described among Messrs. Watson’s
instruments, page 108.
The Stand.—A good firm stand is undoubtedly of the first importance for all
high-class work. The steadiness of the instrument and its entire freedom
from vibration depends largely upon the form of the stand. I am glad to find
Dr. Crookshank in accord with me as to the Ross-Jackson model, one which,
in my opinion, has not been entirely superseded by models of a more recent
date. Indeed, the latest improvement effected in the Ross-Jackson form, in
which attention has been given to the spreading-out of the feet, has
Page 177
converted it into as solid and firm a stand as Powell’s; it is equally free from
vibration when placed in the horizontal position.
There are, however, four different forms of stands—the tripod; the plate with
double columns; the single column ending in a plate or a bent claw; and the
horse shoe. The tripod stand, with cork feet, is by far the steadiest form of
model. The single upright pillar support should unquestionably be
condemned, as it admits of considerable vibration, and is most inconvenient
for laboratory work. The heavy horse-shoe form is compact and firm, and
the weight of it can hardly be considered an objection.
The Tubular Body is from eight to ten inches in length, to which is added a
draw-tube with an engraved millimetre scale. By extending the draw-tube
greater magnification is obtained, but since this is at the cost of definition it
should hardly ever be employed in the examination of bacteria. A Triple
Nose-piece is doubtless a convenience, saving time which is otherwise spent
in replacing objectives of different magnifying powers; there is also less risk
of injuring them. Focus should be obtained by means of a rack and pinion
coarse adjustment, together with the most approved kind of fine adjustment.
The sliding tube cannot be recommended, as the motion may be stiff,
encouraging the use of force, which in turn may result in the objective being
brought violently into contact with the specimen, thus doing injury to the
lens or damage to the preparation; or it may get too loose and readily slip out
of focus.
The Stage should be flat and rigid, either rectangular or circular, so long as it
is sufficiently large to accommodate plate cultivation. A removable
mechanical stage is of great advantage for working with high powers, as a
motile bacterium can be constantly kept in view, while one hand is engaged
in working the fine adjustment; it may also be employed as a finder, if
engraved with a longitudinal and vertical scale, and provided with a stop.
The mechanical stage must be removable, so that the stage proper may be
free from any attachments when required for the examination of cultures.
Diaphragms.—The plan of using a series of separate discs of different sizes
should be avoided, as they are easily lost, and bacteriological investigations
may have to be made under conditions in which it is difficult to replace
vibration when placed in the horizontal position.
There are, however, four different forms of stands—the tripod; the plate with
double columns; the single column ending in a plate or a bent claw; and the
horse shoe. The tripod stand, with cork feet, is by far the steadiest form of
model. The single upright pillar support should unquestionably be
condemned, as it admits of considerable vibration, and is most inconvenient
for laboratory work. The heavy horse-shoe form is compact and firm, and
the weight of it can hardly be considered an objection.
The Tubular Body is from eight to ten inches in length, to which is added a
draw-tube with an engraved millimetre scale. By extending the draw-tube
greater magnification is obtained, but since this is at the cost of definition it
should hardly ever be employed in the examination of bacteria. A Triple
Nose-piece is doubtless a convenience, saving time which is otherwise spent
in replacing objectives of different magnifying powers; there is also less risk
of injuring them. Focus should be obtained by means of a rack and pinion
coarse adjustment, together with the most approved kind of fine adjustment.
The sliding tube cannot be recommended, as the motion may be stiff,
encouraging the use of force, which in turn may result in the objective being
brought violently into contact with the specimen, thus doing injury to the
lens or damage to the preparation; or it may get too loose and readily slip out
of focus.
The Stage should be flat and rigid, either rectangular or circular, so long as it
is sufficiently large to accommodate plate cultivation. A removable
mechanical stage is of great advantage for working with high powers, as a
motile bacterium can be constantly kept in view, while one hand is engaged
in working the fine adjustment; it may also be employed as a finder, if
engraved with a longitudinal and vertical scale, and provided with a stop.
The mechanical stage must be removable, so that the stage proper may be
free from any attachments when required for the examination of cultures.
Diaphragms.—The plan of using a series of separate discs of different sizes
should be avoided, as they are easily lost, and bacteriological investigations
may have to be made under conditions in which it is difficult to replace
Page 178
them. A better plan is a revolving plate with apertures of different sizes, but
the most convenient form is the iris diaphragm.
The Sub-stage Condenser is as necessary in biological work as in the
objective—in fact, the condenser and the objective should be considered as
forming one piece of optical apparatus; the microscope must be regarded as
incomplete without it.
It is by the sub-stage condenser that the rays of light are concentrated at one
point, or on one particular bacterium; for the best definition it is essential
that there should be mechanical arrangements for accurately centring and
focussing the condenser. All this will be explained and enlarged upon under
“Practical Optics.”
In the historical review presented to my readers on the evolution of the
modern microscope, I have for the most part relied upon my long and close
association, extending over a period of upwards of half a century, with
microscopy. I need hardly say I could have very much extended my remarks
with pleasure and profit had space permitted, and thereby much increased
the number of names of manufacturers, who have well-established
reputations for the quality of their work, and whose instruments, more or less
complete in design, realise the wants of students and of that large class of
present-day workers engaged in microscopical pursuits to whom economy of
outlay is almost a first consideration. No valid reason, however, can be
assigned for splitting up, as some writers do, the several forms of
microscopes into some six different classes, which implies inferiority in
mechanical details or finish, whereas the difference wholly consists in
luxurious appliances to save time, and in accessories for special work or
original research. Before bringing these remarks to a close, it is my wish to
direct the student’s attention to one or two points of importance in
connection with the use of the instrument, viz.: variations in body-lengths of
microscopes, especially between those of English and of Continental
manufacture. The optical-standard measurement adopted in this country for
the body-tube-length is 10 inches; and for its mechanical, 8¾ inches. That of
Continental opticians is, optical-tube-length 7·08 inches, or 180 mm.; the
mechanical, 6·3 inches = to 168 mm.
the most convenient form is the iris diaphragm.
The Sub-stage Condenser is as necessary in biological work as in the
objective—in fact, the condenser and the objective should be considered as
forming one piece of optical apparatus; the microscope must be regarded as
incomplete without it.
It is by the sub-stage condenser that the rays of light are concentrated at one
point, or on one particular bacterium; for the best definition it is essential
that there should be mechanical arrangements for accurately centring and
focussing the condenser. All this will be explained and enlarged upon under
“Practical Optics.”
In the historical review presented to my readers on the evolution of the
modern microscope, I have for the most part relied upon my long and close
association, extending over a period of upwards of half a century, with
microscopy. I need hardly say I could have very much extended my remarks
with pleasure and profit had space permitted, and thereby much increased
the number of names of manufacturers, who have well-established
reputations for the quality of their work, and whose instruments, more or less
complete in design, realise the wants of students and of that large class of
present-day workers engaged in microscopical pursuits to whom economy of
outlay is almost a first consideration. No valid reason, however, can be
assigned for splitting up, as some writers do, the several forms of
microscopes into some six different classes, which implies inferiority in
mechanical details or finish, whereas the difference wholly consists in
luxurious appliances to save time, and in accessories for special work or
original research. Before bringing these remarks to a close, it is my wish to
direct the student’s attention to one or two points of importance in
connection with the use of the instrument, viz.: variations in body-lengths of
microscopes, especially between those of English and of Continental
manufacture. The optical-standard measurement adopted in this country for
the body-tube-length is 10 inches; and for its mechanical, 8¾ inches. That of
Continental opticians is, optical-tube-length 7·08 inches, or 180 mm.; the
mechanical, 6·3 inches = to 168 mm.
Page 179
Professor Abbe constructed an apochromatic immersion objective especially
for the English optical tube-length of 10·6 inches (= to 270 m.m.), and
mechanical tube-length somewhat less in measurement. This may be taken
to mean a slight increase in the standard value of the tube, and therefore the
addition of the rack-and-pinion to the draw-tube, now generally made a part
of the microscope, is certainly of some practical value. This difference,
however, when working with the English body-tube of 10 inches, may be
discarded; it is, in fact, only where the shorter Continental body is in use,
that so small a difference of tube-length exercises a disturbing effect over
adjustment. Moreover, an object placed on the stage of the shorter body
microscope will not be seen with the same distinctness by the draughtsman
should he wish to make use of the camera lucida.
The optical tube-length of the body is measured from the back lens of the
objective to the front lens or principal focus of the eye-piece; the mechanical
tube-length from the end of nose-piece of objective to the top lens of the
eye-piece.
for the English optical tube-length of 10·6 inches (= to 270 m.m.), and
mechanical tube-length somewhat less in measurement. This may be taken
to mean a slight increase in the standard value of the tube, and therefore the
addition of the rack-and-pinion to the draw-tube, now generally made a part
of the microscope, is certainly of some practical value. This difference,
however, when working with the English body-tube of 10 inches, may be
discarded; it is, in fact, only where the shorter Continental body is in use,
that so small a difference of tube-length exercises a disturbing effect over
adjustment. Moreover, an object placed on the stage of the shorter body
microscope will not be seen with the same distinctness by the draughtsman
should he wish to make use of the camera lucida.
The optical tube-length of the body is measured from the back lens of the
objective to the front lens or principal focus of the eye-piece; the mechanical
tube-length from the end of nose-piece of objective to the top lens of the
eye-piece.
Page 180
The Hartnach Students’ Model Microscope.
Page 181
CHAPTER III.
Applied Optics:—Eye-pieces; Achromatic Objectives; Condensers.
It is almost unnecessary to say that the eye-piece forms a most important
part of applied optics in the microscope. It is an optical combination
designed to bring the pencil of rays from the objective to assist in the
formation of a real or virtual image before it arrives at the eye of the
observer. Greater attention has been given of late years to the improvement
of the eye-piece, since flatness of field much depends upon it. Opticians
have therefore sought to make it both achromatic and compensatory.
There are several forms of eye-pieces in use, some of which partake of a
special character, and these will receive attention in their proper places. It is,
however, customary among English opticians to denote the value of their
several eye-pieces by Roman capitals, A, B, C, D, and E. Continental
opticians, on the other hand, have a preference for numerals, 1, 2, 3, 4, 5 and
6, or more, and by which they are recognised.
The eye-piece in more general use is that known as the Huyghenian (Fig.
99); this came into use upwards of two centuries ago. It was constructed by
Christian Huyghens, a Dutch philosopher and eminent man of science,
secretary to William III.
It was made for the eye-piece of a telescope he constructed with his own
hands, and it has been in constant use as the eye-piece of the microscope for
nearly two centuries. It consists of two plano-convex lenses, with their plane
surfaces turned towards the eye, and divided at a distance equal to half the
sum of their focal lengths—in other words, at half the sum of the focal
length of the eye-glass and of the distance from the field-glass at which an
image from the object glass would be formed, a stop, or diaphragm, being
placed between the two lenses for the reason about to be explained.
Applied Optics:—Eye-pieces; Achromatic Objectives; Condensers.
It is almost unnecessary to say that the eye-piece forms a most important
part of applied optics in the microscope. It is an optical combination
designed to bring the pencil of rays from the objective to assist in the
formation of a real or virtual image before it arrives at the eye of the
observer. Greater attention has been given of late years to the improvement
of the eye-piece, since flatness of field much depends upon it. Opticians
have therefore sought to make it both achromatic and compensatory.
There are several forms of eye-pieces in use, some of which partake of a
special character, and these will receive attention in their proper places. It is,
however, customary among English opticians to denote the value of their
several eye-pieces by Roman capitals, A, B, C, D, and E. Continental
opticians, on the other hand, have a preference for numerals, 1, 2, 3, 4, 5 and
6, or more, and by which they are recognised.
The eye-piece in more general use is that known as the Huyghenian (Fig.
99); this came into use upwards of two centuries ago. It was constructed by
Christian Huyghens, a Dutch philosopher and eminent man of science,
secretary to William III.
It was made for the eye-piece of a telescope he constructed with his own
hands, and it has been in constant use as the eye-piece of the microscope for
nearly two centuries. It consists of two plano-convex lenses, with their plane
surfaces turned towards the eye, and divided at a distance equal to half the
sum of their focal lengths—in other words, at half the sum of the focal
length of the eye-glass and of the distance from the field-glass at which an
image from the object glass would be formed, a stop, or diaphragm, being
placed between the two lenses for the reason about to be explained.
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Huyghens himself appears to have been quite unaware of the value of an
eye-piece so cleverly constructed.
It was reserved for Boscovich to
point out that, by this important
arrangement, he had corrected a
portion of the chromatic
aberration incidental to the earlier
form of eye-pieces. Let Fig. 100
represent the Huyghenian eye-
piece of a microscope, f f being
the field-glass, and e e the eye-
glass, and l m n the two extreme
rays of each of the three pencils
emanating from the centre and
ends of the object, of which, but
for the field-glass, a series of
coloured images would be formed
from r r to b b; those near r r
being red, those near b b blue, and
Fig. 99.—Huyghenian Eye-piece A, the dotted lines the intermediate ones green,
show position of lenses. yellow, and so on, corresponding
with the colours of the prismatic
Spectrum.
The effect described, that of projecting the blue image beyond the red, over-
correcting the object-glass as to colour, is purposely produced; it is also seen
that the images b b and r r are curved in the wrong direction to be seen
distinctly by the convex eye-lens; this then is a further defect of the
compound microscope made up of two lenses. But the field-glass, at the
same time that it bends the rays and converges them to foci at b′ b′ and r′ r′,
also reverses the curvature of the images as here shown, giving them the
form best adapted for distinct vision by the eye-glass e e. The field-glass has
at the same time brought the blue and red images closer together, so that they
produce an almost colourless image to the eye. The chromatic aberration of
lenses has been clearly explained in a previous chapter. But let it be
supposed that the object-glass had not been over-corrected, that it had been
perfectly achromatic; the rays would then have appeared coloured as soon as
eye-piece so cleverly constructed.
It was reserved for Boscovich to
point out that, by this important
arrangement, he had corrected a
portion of the chromatic
aberration incidental to the earlier
form of eye-pieces. Let Fig. 100
represent the Huyghenian eye-
piece of a microscope, f f being
the field-glass, and e e the eye-
glass, and l m n the two extreme
rays of each of the three pencils
emanating from the centre and
ends of the object, of which, but
for the field-glass, a series of
coloured images would be formed
from r r to b b; those near r r
being red, those near b b blue, and
Fig. 99.—Huyghenian Eye-piece A, the dotted lines the intermediate ones green,
show position of lenses. yellow, and so on, corresponding
with the colours of the prismatic
Spectrum.
The effect described, that of projecting the blue image beyond the red, over-
correcting the object-glass as to colour, is purposely produced; it is also seen
that the images b b and r r are curved in the wrong direction to be seen
distinctly by the convex eye-lens; this then is a further defect of the
compound microscope made up of two lenses. But the field-glass, at the
same time that it bends the rays and converges them to foci at b′ b′ and r′ r′,
also reverses the curvature of the images as here shown, giving them the
form best adapted for distinct vision by the eye-glass e e. The field-glass has
at the same time brought the blue and red images closer together, so that they
produce an almost colourless image to the eye. The chromatic aberration of
lenses has been clearly explained in a previous chapter. But let it be
supposed that the object-glass had not been over-corrected, that it had been
perfectly achromatic; the rays would then have appeared coloured as soon as
Page 183
they had passed the field-glass; the blue rays of the central pencil, for
example, would converge at b′′, and the red rays at r′′, which is just the
reverse of what is required of the eye-lens; for as its blue focus is also
shorter than its red, it would require that the blue image should be at r′′, and
the red at b′′. This effect is due to over-correction of the object-glass, which
removes the blue foci b b as much beyond the red foci r r as the sum of the
distances between the red and the blue foci of the field-lens and eye-lens; so
that the separation b r is exactly taken up in passing through those two
lenses, and the several colours coincide, so far as focal distance is
concerned, as the rays pass the eye-lens. So that while they coincide as to
distance, they differ in another respect—the blue image is rendered smaller
than the red by the greater refractive power of the field-glass upon the
former. In tracing the pencil l, for instance, it will be noticed that, after
passing the field-glass, two sets of lines are drawn, one whole and one
dotted, the former representing the red, and the latter the blue rays. This
accidental effect in the Huyghenian eye-piece was pointed out by Boscovich.
The separation into colours of the field-glass is like the over-correction of
the object-glass—and opens the way to its complete correction. If the
differently-coloured rays were kept together till they reached the eye-glass,
they would still be coloured, and present coloured images to the eye. The
separating effected by the field-glass causes the blue rays to fall so much
nearer the centre of the eye-glass, where, owing to its spherical figure, the
refractive power is less than at the margin, so that spherical error of the eye-
lens may be said to constitute a nearly equal balance to the chromatic
dispersion of the field-lens, and the blue and red rays l′ and l′′ emerge nearly
parallel, presenting a fairly good definition of a single point to the eye. The
same may be said of the intermediate colours of the other pencils. The eye-
glass thus constructed not only brings together the images b′ b′, r′ r′, but it
likewise has the most important effect of rendering them flatter, and assisting
in the correction of chromatic and spherical aberration.
example, would converge at b′′, and the red rays at r′′, which is just the
reverse of what is required of the eye-lens; for as its blue focus is also
shorter than its red, it would require that the blue image should be at r′′, and
the red at b′′. This effect is due to over-correction of the object-glass, which
removes the blue foci b b as much beyond the red foci r r as the sum of the
distances between the red and the blue foci of the field-lens and eye-lens; so
that the separation b r is exactly taken up in passing through those two
lenses, and the several colours coincide, so far as focal distance is
concerned, as the rays pass the eye-lens. So that while they coincide as to
distance, they differ in another respect—the blue image is rendered smaller
than the red by the greater refractive power of the field-glass upon the
former. In tracing the pencil l, for instance, it will be noticed that, after
passing the field-glass, two sets of lines are drawn, one whole and one
dotted, the former representing the red, and the latter the blue rays. This
accidental effect in the Huyghenian eye-piece was pointed out by Boscovich.
The separation into colours of the field-glass is like the over-correction of
the object-glass—and opens the way to its complete correction. If the
differently-coloured rays were kept together till they reached the eye-glass,
they would still be coloured, and present coloured images to the eye. The
separating effected by the field-glass causes the blue rays to fall so much
nearer the centre of the eye-glass, where, owing to its spherical figure, the
refractive power is less than at the margin, so that spherical error of the eye-
lens may be said to constitute a nearly equal balance to the chromatic
dispersion of the field-lens, and the blue and red rays l′ and l′′ emerge nearly
parallel, presenting a fairly good definition of a single point to the eye. The
same may be said of the intermediate colours of the other pencils. The eye-
glass thus constructed not only brings together the images b′ b′, r′ r′, but it
likewise has the most important effect of rendering them flatter, and assisting
in the correction of chromatic and spherical aberration.
Page 184
Fig. 100.—Huyghenian Eye-piece.
Fig. 101.—Ramsden’s Eye-piece.
The later form of the Huyghenian eye-piece is that of the late Sir George
Airy, the field-glass of which is a meniscus with the convex side turned
towards the objective, and the eye-lens a crossed convex with its flatter side
towards the eye. Another negative eye-piece is that known as the Kellner, or
orthoscopic eye-piece. It consists of a bi-convex field-glass and an
Fig. 101.—Ramsden’s Eye-piece.
The later form of the Huyghenian eye-piece is that of the late Sir George
Airy, the field-glass of which is a meniscus with the convex side turned
towards the objective, and the eye-lens a crossed convex with its flatter side
towards the eye. Another negative eye-piece is that known as the Kellner, or
orthoscopic eye-piece. It consists of a bi-convex field-glass and an
Page 185
achromatic doublet eye-lens. This magnifies ten times, but it in no way
compares with the Huyghenian in value. Neither does it afford the same
flatness of field.
The Ramsden, or positive eye-piece, is chiefly employed as a micrometer
eye-piece for the measurement of the values of magnified images. The
construction of this eye-piece is shown in Fig. 101, a divided scale being cut
on a strip of glass in 1⁄100ths of an inch, every fifth of which is cut longer than
the rest to facilitate the reading of the markings, and at the same time that of
the image of the object, both being distinctly seen together, as in the
accompanying reduced micro-photograph of blood corpuscles, Fig. 102.
The value of such measurements in reference to the real object, when once
obtained; is constant for the same objective. It becomes apparent, then, that
the value of the divisions seen in the eye-piece micrometer must be found
with all the objectives used, and carefully tabulated.
It was Mr. Lister who first proposed to place on the stage of the microscope
a divided scale of a certain value. Viewing the scale as a microscopic object,
he observed how many of the divisions on the scale attached to the eye-piece
corresponded with one or more of a magnified image. If, for instance, ten of
those in the eye-piece correspond with one of those in the image, and if the
divisions are known to be equal, then the image is ten times larger than the
object, and the dimensions of the object ten times less than that indicated by
the micrometer. If the divisions on the micrometer and on the magnified
scale are not equal, it becomes a mere rule-of-three sum; but in general this
trouble is taken by the maker of the instrument, who furnishes a table
showing the value of each division of the micrometer for every object-glass
with which it will be employed.
Mr. Jackson’s simple and cheap micrometer is represented in Fig. 103. It
consists of a slip of glass placed in the focus of the eye-glass, with the
divisions sufficiently fine to have the value of the ten-thousandth part of an
inch with the quarter-inch object-glass, and the twenty-thousandth with the
eighth; at the same time the half, or even the quarter of a division may be
estimated, thus affording the means of attaining considerable accuracy, and
may be used to supersede the more complicated and expensive screw-
compares with the Huyghenian in value. Neither does it afford the same
flatness of field.
The Ramsden, or positive eye-piece, is chiefly employed as a micrometer
eye-piece for the measurement of the values of magnified images. The
construction of this eye-piece is shown in Fig. 101, a divided scale being cut
on a strip of glass in 1⁄100ths of an inch, every fifth of which is cut longer than
the rest to facilitate the reading of the markings, and at the same time that of
the image of the object, both being distinctly seen together, as in the
accompanying reduced micro-photograph of blood corpuscles, Fig. 102.
The value of such measurements in reference to the real object, when once
obtained; is constant for the same objective. It becomes apparent, then, that
the value of the divisions seen in the eye-piece micrometer must be found
with all the objectives used, and carefully tabulated.
It was Mr. Lister who first proposed to place on the stage of the microscope
a divided scale of a certain value. Viewing the scale as a microscopic object,
he observed how many of the divisions on the scale attached to the eye-piece
corresponded with one or more of a magnified image. If, for instance, ten of
those in the eye-piece correspond with one of those in the image, and if the
divisions are known to be equal, then the image is ten times larger than the
object, and the dimensions of the object ten times less than that indicated by
the micrometer. If the divisions on the micrometer and on the magnified
scale are not equal, it becomes a mere rule-of-three sum; but in general this
trouble is taken by the maker of the instrument, who furnishes a table
showing the value of each division of the micrometer for every object-glass
with which it will be employed.
Mr. Jackson’s simple and cheap micrometer is represented in Fig. 103. It
consists of a slip of glass placed in the focus of the eye-glass, with the
divisions sufficiently fine to have the value of the ten-thousandth part of an
inch with the quarter-inch object-glass, and the twenty-thousandth with the
eighth; at the same time the half, or even the quarter of a division may be
estimated, thus affording the means of attaining considerable accuracy, and
may be used to supersede the more complicated and expensive screw-
Page 186
micrometer, being handier to use, and
not liable to derangement in
inexperienced hands.
The positive eye-piece affords the
best view of the micrometer, the
negative of the object. The former is
quite free from distortion, even to the
edges of the field; but the object is
slightly coloured. The latter is free
from colour, and is slightly distorted
at the edges. In the centre of the field, Fig. 102.—Blood Corpuscles and Micrometer,
magnified 1·3500.
however, to the extent of half its
diameter, there is no perceptible
distortion, and the clearness of the definition gives a precision to the
measurement which is very satisfactory.
Short bold lines are ruled on a piece
of glass, a, Fig. 103, to facilitate
counting, the fifth is drawn longer,
and the tenth still longer, as in the
common rule. Very fine levigated
plumbago is rubbed into the lines to
render them visible; they are then
covered with a piece of thin glass,
cemented by Canada balsam, to
prevent the plumbago from being
wiped out. The slip of glass thus
prepared is secured in a thin brass
frame, so that it may slide freely into
its place.
Fig. 103.—Jackson’s Eye-piece Micrometer.
Slips are cut in the negative eye-piece
on each side, so that the brass frame may be pressed across the field in the
focus of the eye-glass, as at m; the cell of which should have a longer screw
than usual, to admit of adjustment for different eyes. The brass frame is
retained in its place by a spring within the tube of the eye-piece; and in using
it the object is brought to the centre of the field by the stage movements; the
not liable to derangement in
inexperienced hands.
The positive eye-piece affords the
best view of the micrometer, the
negative of the object. The former is
quite free from distortion, even to the
edges of the field; but the object is
slightly coloured. The latter is free
from colour, and is slightly distorted
at the edges. In the centre of the field, Fig. 102.—Blood Corpuscles and Micrometer,
magnified 1·3500.
however, to the extent of half its
diameter, there is no perceptible
distortion, and the clearness of the definition gives a precision to the
measurement which is very satisfactory.
Short bold lines are ruled on a piece
of glass, a, Fig. 103, to facilitate
counting, the fifth is drawn longer,
and the tenth still longer, as in the
common rule. Very fine levigated
plumbago is rubbed into the lines to
render them visible; they are then
covered with a piece of thin glass,
cemented by Canada balsam, to
prevent the plumbago from being
wiped out. The slip of glass thus
prepared is secured in a thin brass
frame, so that it may slide freely into
its place.
Fig. 103.—Jackson’s Eye-piece Micrometer.
Slips are cut in the negative eye-piece
on each side, so that the brass frame may be pressed across the field in the
focus of the eye-glass, as at m; the cell of which should have a longer screw
than usual, to admit of adjustment for different eyes. The brass frame is
retained in its place by a spring within the tube of the eye-piece; and in using
it the object is brought to the centre of the field by the stage movements; the
Page 187
coincidence between one side of it and one of the long lines is made with
great accuracy by means of the small screw acting upon the slip of glass.
The divisions are then read off as easily as the inches and tenths on a
common rule. The operation, indeed, is nothing more than the laying of a
rule across the body to be measured; and it matters not whether the object be
transparent or opaque, mounted or unmounted, if its edges can be distinctly
seen, its diameter can be taken.
Previously, however, to using the micrometer, the value of its divisions
should be ascertained with each object-glass; the method of doing this is as
follows:—
Place a slip of ruled glass on the stage; and having turned the eye-piece so
that the lines on the two glasses are parallel, read off the number of divisions
in the eye-piece which cover one on the stage. Repeat this process with
different portions of the stage-micrometer, and if there be a difference, take
the mean. Suppose the hundredth of an inch on the stage requires eighteen
divisions in the eye-piece to cover it; it is plain that an inch would require
eighteen hundred, and an object which occupied nine of these divisions
would measure the two-hundredth of an inch. Take the instance supposed,
and let the microscope be furnished with a draw-tube, marked on the side
with inches and tenths. By drawing this out a short distance, the image of the
stage micrometer will be expanded until one division is covered by twenty in
the eye-piece. These will then have the value of two-thousandths of an inch,
and the object which before measured nine will then measure ten; which,
divided by 2,000, gives the decimal fraction ·005.
Enter in a table the length to which the tube is drawn out, and the number of
divisions on the eye-piece micrometer equivalent to an inch on the stage; and
any measurements afterwards taken with the same micrometer and object-
glass may, by a short process of mental arithmetic, be reduced to the decimal
parts of an inch, if not actually observed in them.
In ascertaining the value of the micrometer with a deep objective, if the
hundredth of an inch on the stage occupies too much of the field, then the
two-hundredth or five-hundredth should be used and the number of the
divisions corresponding to that quantity be multiplied by two hundred or five
hundred, as the case may be.
great accuracy by means of the small screw acting upon the slip of glass.
The divisions are then read off as easily as the inches and tenths on a
common rule. The operation, indeed, is nothing more than the laying of a
rule across the body to be measured; and it matters not whether the object be
transparent or opaque, mounted or unmounted, if its edges can be distinctly
seen, its diameter can be taken.
Previously, however, to using the micrometer, the value of its divisions
should be ascertained with each object-glass; the method of doing this is as
follows:—
Place a slip of ruled glass on the stage; and having turned the eye-piece so
that the lines on the two glasses are parallel, read off the number of divisions
in the eye-piece which cover one on the stage. Repeat this process with
different portions of the stage-micrometer, and if there be a difference, take
the mean. Suppose the hundredth of an inch on the stage requires eighteen
divisions in the eye-piece to cover it; it is plain that an inch would require
eighteen hundred, and an object which occupied nine of these divisions
would measure the two-hundredth of an inch. Take the instance supposed,
and let the microscope be furnished with a draw-tube, marked on the side
with inches and tenths. By drawing this out a short distance, the image of the
stage micrometer will be expanded until one division is covered by twenty in
the eye-piece. These will then have the value of two-thousandths of an inch,
and the object which before measured nine will then measure ten; which,
divided by 2,000, gives the decimal fraction ·005.
Enter in a table the length to which the tube is drawn out, and the number of
divisions on the eye-piece micrometer equivalent to an inch on the stage; and
any measurements afterwards taken with the same micrometer and object-
glass may, by a short process of mental arithmetic, be reduced to the decimal
parts of an inch, if not actually observed in them.
In ascertaining the value of the micrometer with a deep objective, if the
hundredth of an inch on the stage occupies too much of the field, then the
two-hundredth or five-hundredth should be used and the number of the
divisions corresponding to that quantity be multiplied by two hundred or five
hundred, as the case may be.
Page 188
The micrometer should not be fitted into too deep an eye-piece, as it is
essential to preserve good definition. A middle-power Kellner or
Huyghenian is frequently employed; at all events, use the eye-piece of lower
power rather than impair the image.
The eye-lens above the micrometer should not be of shorter focus than three-
quarters of an inch, even with high-power objectives.
The Ramsden Eye-piece.—The cobweb micrometer is the most efficient
piece of apparatus yet brought into use for measuring the magnified image.
It is made by stretching across the field of the eye-piece two extremely fine
parallel wires or cobwebs, one or both of which can be separated by the
action of a micrometer screw, the trap head of which is divided into a
hundred or more equal parts, which successively pass by an index as the
milled head is turned, shown in Fig. 104. A portion of the field of view is cut
off at right angles to the filaments by a scale formed of a thin plate of brass
having notches at its edges, the distances between which correspond to the
threads of the screw, every fifth notch (as in the previous case) being made
deeper than the rest, to make the work of enumeration easier. The number of
entire divisions on the scale shows then how many complete turns of the
screw have been made in the separation of the wires, while the number of
index points on the milled head shows the value to the fraction of a turn, that
may have been made in addition. A screw with one hundred threads to the
inch is that usually employed; this gives to each division in the scale in the
eye-piece the value of 1⁄100th of an inch. The edge of the milled head is also
divided into the same number of parts.
Micrometer
scale to drop
into Eye-piece.
essential to preserve good definition. A middle-power Kellner or
Huyghenian is frequently employed; at all events, use the eye-piece of lower
power rather than impair the image.
The eye-lens above the micrometer should not be of shorter focus than three-
quarters of an inch, even with high-power objectives.
The Ramsden Eye-piece.—The cobweb micrometer is the most efficient
piece of apparatus yet brought into use for measuring the magnified image.
It is made by stretching across the field of the eye-piece two extremely fine
parallel wires or cobwebs, one or both of which can be separated by the
action of a micrometer screw, the trap head of which is divided into a
hundred or more equal parts, which successively pass by an index as the
milled head is turned, shown in Fig. 104. A portion of the field of view is cut
off at right angles to the filaments by a scale formed of a thin plate of brass
having notches at its edges, the distances between which correspond to the
threads of the screw, every fifth notch (as in the previous case) being made
deeper than the rest, to make the work of enumeration easier. The number of
entire divisions on the scale shows then how many complete turns of the
screw have been made in the separation of the wires, while the number of
index points on the milled head shows the value to the fraction of a turn, that
may have been made in addition. A screw with one hundred threads to the
inch is that usually employed; this gives to each division in the scale in the
eye-piece the value of 1⁄100th of an inch. The edge of the milled head is also
divided into the same number of parts.
Micrometer
scale to drop
into Eye-piece.
Page 189
Fig. 104.—Ramsden Screw Micrometer Eye-piece.
In Watson’s Ramsden screw micrometer, Fig. 104, the micrometer scale
(seen detached) is ruled on a circular piece of glass, and this, by unscrewing
the top, is dropped into its place, and one of the wires, both being fixed, is
set a little to the side of the field, the teeth of the screw being cut to 1⁄100ths,
and the drum giving the fractional space between the teeth to 1⁄100ths, so that
the 1⁄10000th of an inch can be read off. This micrometer eye-piece is
constructed entirely of aluminium, a decided advantage, being so much
lighter than brass to handle.
In the screw micrometer of other makers, other modifications are found. An
iris diaphragm being placed below the web to suit the power of the eye-piece
employed, a guiding line at right angles to the web is sometimes added. Care
should be taken to see that when the movable web coincides exactly with the
fixed web, the indicator on the graduated head stands at zero.
The Compensating Eye-piece.—The very important improvements effected
in the construction of the objective naturally led up to an equally useful
change for the better in the eye-piece.
All objectives of wide aperture, from the curvature of their hemispherical
front lenses, show a certain amount of colour defect in the extra-axial
portion of the field, even if perfectly achromatic in the centre. Whether an
image be directly projected by the objective, or whether it be examined with
an aplanatic eye-piece, colour fringes may be detected, possibly in an
increasing degree towards the periphery. This residual chromatic aberration
has at length been very nearly eliminated by the aid of the compensating
eye-piece.
The construction of compensating eye-pieces is somewhat remarkable, since
they have an equivalent error in an opposite direction—that is, the image
formed by the red rays is greater than that corresponding to the blue rays;
consequently, eye-pieces so constructed serve to compensate for the unequal
magnification produced by different coloured rays, and images appear free
from colour up to the margin of the field.
In Watson’s Ramsden screw micrometer, Fig. 104, the micrometer scale
(seen detached) is ruled on a circular piece of glass, and this, by unscrewing
the top, is dropped into its place, and one of the wires, both being fixed, is
set a little to the side of the field, the teeth of the screw being cut to 1⁄100ths,
and the drum giving the fractional space between the teeth to 1⁄100ths, so that
the 1⁄10000th of an inch can be read off. This micrometer eye-piece is
constructed entirely of aluminium, a decided advantage, being so much
lighter than brass to handle.
In the screw micrometer of other makers, other modifications are found. An
iris diaphragm being placed below the web to suit the power of the eye-piece
employed, a guiding line at right angles to the web is sometimes added. Care
should be taken to see that when the movable web coincides exactly with the
fixed web, the indicator on the graduated head stands at zero.
The Compensating Eye-piece.—The very important improvements effected
in the construction of the objective naturally led up to an equally useful
change for the better in the eye-piece.
All objectives of wide aperture, from the curvature of their hemispherical
front lenses, show a certain amount of colour defect in the extra-axial
portion of the field, even if perfectly achromatic in the centre. Whether an
image be directly projected by the objective, or whether it be examined with
an aplanatic eye-piece, colour fringes may be detected, possibly in an
increasing degree towards the periphery. This residual chromatic aberration
has at length been very nearly eliminated by the aid of the compensating
eye-piece.
The construction of compensating eye-pieces is somewhat remarkable, since
they have an equivalent error in an opposite direction—that is, the image
formed by the red rays is greater than that corresponding to the blue rays;
consequently, eye-pieces so constructed serve to compensate for the unequal
magnification produced by different coloured rays, and images appear free
from colour up to the margin of the field.
Page 190
Zeiss’s compensating eye-pieces are so arranged that the lower focal points
of each series lie in the same plane when inserted in the body-tube of the
microscope; no alteration of focus is therefore required on changing one eye-
piece for another. This of itself is not only an advantage but also a saving of
time, while the distance between the upper focal point of the objective and
the lower one of the eye-piece, which is the determining element of
magnification, remains constant.
Fig. 105.—A sectional view of Zeiss’s Compensating series of Eye-pieces, ½ the
full size.
A.—Plane of the upper edge of the tube.
B.—Lower focal plane of eye-pieces, with their lenses in situ.
of each series lie in the same plane when inserted in the body-tube of the
microscope; no alteration of focus is therefore required on changing one eye-
piece for another. This of itself is not only an advantage but also a saving of
time, while the distance between the upper focal point of the objective and
the lower one of the eye-piece, which is the determining element of
magnification, remains constant.
Fig. 105.—A sectional view of Zeiss’s Compensating series of Eye-pieces, ½ the
full size.
A.—Plane of the upper edge of the tube.
B.—Lower focal plane of eye-pieces, with their lenses in situ.
Page 191
The ordinary working eye-pieces, Huyghenian and others, commencing with
a magnification of four diameters, are so constructed that they can be
conveniently used, as we are accustomed to use them in England, with high
powers, Zeiss’s Nos. 12 and 18 compensating eye-pieces being adapted for
use with his lower power apochromatic lenses of 16 and 8 mm. The
numbering of the eye-pieces is carried out on the plan originally proposed by
Professor Abbe—that is, the number denotes how many times an eye-piece,
when employed with a given tube-length, increases the initial magnifying
power of the objective, and at the same time furnishes figures for their
rational enumeration. It is on this basis that the German compensating eye-
pieces have been arranged in series, and in agreement with their magnifying
power and distinctive numberings of 2, 4, 6, 8, 12, 18. Of these several eye-
pieces, 12 is found to be the most useful. The magnification obtained by
combining a compensating eye-piece with any apochromatic objective is
found by multiplying its number by the initial magnification of the objective,
as given in the following proof:—An objective of 3·0 mm. focus, for
example, gives in itself a magnification of 83·3 (calculated, for the
conventional distance of vision, 250 mm.); eye-piece 12 therefore gives with
this objective a magnification of 12 × 83·3 = 1000 diameters. The
classification, however, of these eye-pieces, as furnished by Abbe, is
dependent upon increase in the total magnifying power of the microscope
obtained by means of the eye-piece as compared with that given by the
objective alone. The numbering, then, denotes how many times an eye-piece
increases the magnifying power of the objective when used with a given
body-tube; the proper measure of the eye-piece magnification; and, at the
same time, the figures for rational enumeration.
a magnification of four diameters, are so constructed that they can be
conveniently used, as we are accustomed to use them in England, with high
powers, Zeiss’s Nos. 12 and 18 compensating eye-pieces being adapted for
use with his lower power apochromatic lenses of 16 and 8 mm. The
numbering of the eye-pieces is carried out on the plan originally proposed by
Professor Abbe—that is, the number denotes how many times an eye-piece,
when employed with a given tube-length, increases the initial magnifying
power of the objective, and at the same time furnishes figures for their
rational enumeration. It is on this basis that the German compensating eye-
pieces have been arranged in series, and in agreement with their magnifying
power and distinctive numberings of 2, 4, 6, 8, 12, 18. Of these several eye-
pieces, 12 is found to be the most useful. The magnification obtained by
combining a compensating eye-piece with any apochromatic objective is
found by multiplying its number by the initial magnification of the objective,
as given in the following proof:—An objective of 3·0 mm. focus, for
example, gives in itself a magnification of 83·3 (calculated, for the
conventional distance of vision, 250 mm.); eye-piece 12 therefore gives with
this objective a magnification of 12 × 83·3 = 1000 diameters. The
classification, however, of these eye-pieces, as furnished by Abbe, is
dependent upon increase in the total magnifying power of the microscope
obtained by means of the eye-piece as compared with that given by the
objective alone. The numbering, then, denotes how many times an eye-piece
increases the magnifying power of the objective when used with a given
body-tube; the proper measure of the eye-piece magnification; and, at the
same time, the figures for rational enumeration.
Page 192
Fig. 106.—B and C Achromatic Eye-pieces.
Compensating eye-pieces have been introduced for the correction of certain
errors in high-power objectives—those made with hemispherical fronts. All
such lenses, whether apochromatic or not, are greatly improved by the
compensating eye-piece, but the dry objective and the lower powers are
certainly deteriorated. The lower power compensating eye-pieces are
Huyghenian, the higher are combinations, with no field-lens, and therefore
in working act as a single or positive eye-piece. This is of importance to
those who work with low powers—the older forms of objectives.
Messrs. Watson and Swift have adopted a new formula for their series of
achromatic eye-pieces, whereby their magnification and flatness of field are
improved. These also bear a constant ratio to the initial power of their
objectives.
The compensating eye-pieces of these makers are constructed on the same
principle as those of Zeiss’s for the correction of errors of colour in the
marginal portion of the field, and consequently are in every way as effective
as those of Continental manufacture. Figs. 106, 107, and 108 show in dotted
outline the form and position of the several lenses combined in these eye-
pieces.
Projection Eye-pieces are chiefly used in micro-photography, and for screen
demonstrations. The cap of this eye-piece is provided with a spiral
adjustment for focussing, the diaphragm being placed in front of the eye-
Compensating eye-pieces have been introduced for the correction of certain
errors in high-power objectives—those made with hemispherical fronts. All
such lenses, whether apochromatic or not, are greatly improved by the
compensating eye-piece, but the dry objective and the lower powers are
certainly deteriorated. The lower power compensating eye-pieces are
Huyghenian, the higher are combinations, with no field-lens, and therefore
in working act as a single or positive eye-piece. This is of importance to
those who work with low powers—the older forms of objectives.
Messrs. Watson and Swift have adopted a new formula for their series of
achromatic eye-pieces, whereby their magnification and flatness of field are
improved. These also bear a constant ratio to the initial power of their
objectives.
The compensating eye-pieces of these makers are constructed on the same
principle as those of Zeiss’s for the correction of errors of colour in the
marginal portion of the field, and consequently are in every way as effective
as those of Continental manufacture. Figs. 106, 107, and 108 show in dotted
outline the form and position of the several lenses combined in these eye-
pieces.
Projection Eye-pieces are chiefly used in micro-photography, and for screen
demonstrations. The cap of this eye-piece is provided with a spiral
adjustment for focussing, the diaphragm being placed in front of the eye-
Page 193
lens, an essential arrangement for obtaining an accurate focus. The ring seen
below the cap, Fig. 108, is graduated so that the rotation for distance of
screen may be carefully recorded.
Fig. 107.—The Compensating Eye-piece. Fig. 108.—Projection Eye-piece.
Schmidt’s goniometer positive eye-piece, for measuring the angles of
crystals, is so arranged as to be easily rotated within a large and accurately
graduated circle. In the focus of the eye-piece a single cobweb is drawn
across, and to the upper part is attached a vernier. The crystals being placed
in the field of the microscope, care being taken that they lie perfectly flat, the
vernier is brought to zero, and then the whole apparatus turned until the line
is parallel with one face of the crystal; the frame-work bearing the cobweb,
with the vernier, is now rotated until the cobweb becomes parallel with the
next face of the crystal, and the number of degrees which it has traversed
may then be accurately read off.
below the cap, Fig. 108, is graduated so that the rotation for distance of
screen may be carefully recorded.
Fig. 107.—The Compensating Eye-piece. Fig. 108.—Projection Eye-piece.
Schmidt’s goniometer positive eye-piece, for measuring the angles of
crystals, is so arranged as to be easily rotated within a large and accurately
graduated circle. In the focus of the eye-piece a single cobweb is drawn
across, and to the upper part is attached a vernier. The crystals being placed
in the field of the microscope, care being taken that they lie perfectly flat, the
vernier is brought to zero, and then the whole apparatus turned until the line
is parallel with one face of the crystal; the frame-work bearing the cobweb,
with the vernier, is now rotated until the cobweb becomes parallel with the
next face of the crystal, and the number of degrees which it has traversed
may then be accurately read off.
Page 194
Goniometer.—If a higher degree of precision is required, then, the double-
refracting goniometer invented by the late Dr. Leeson must be substituted.
With this goniometer (Fig. 109) the angles of crystals, whether microscopic
or otherwise, can be measured. It has removed the earlier difficulties
incident to similar instruments formerly in use. Among other advantages, it
is capable of measuring opaque and even imperfect crystals, beside
microscopic crystals and those in the interior of other transparent media. It is
equally applicable to the largest crystals, and will measure angles without
removing the crystal from a specimen, provided only the whole is placed on
a suitable adjusting stage. The value of the goniometer depends on the
application of a doubly refracting prism, either of Iceland spar or of quartz,
cut of such a thickness as will partially separate the two images of the angle
it is proposed to measure.
Dr. Leeson strongly insisted on the importance of the microscope in the
examination of the planes of crystals subjected to measurement, as obliquity
in many cases arises from not only conchoidal fractures, but also from
imperfect laminæ elevating one portion of a plane, and yet allowing a very
tolerable reflection when measured by the double refracting goniometer.
Microscopes for crystallographic and
petrological research are now
specially constructed for measuring
the angles of crystals.
Erector eye-pieces and erecting
prisms are employed for the purpose
of causing the image presented to the
eye to correspond with that of the Fig. 109.—Leeson’s Goniometer.
object. They are also helpful in
making minute dissections of structure; the loss of light, however, by
sending it through two additional surfaces is a drawback, and impairs the
sharpness of the image. Nachet designed an extremely ingenious
arrangement whereby the inverted image became erect; he adapted a simple
rectangular prism to the eye-piece. The obliquity which a prism gives to the
visual rays when the microscope is used in the erect position, as for
dissecting, is an advantage, as it brings the image to the eye at an angle very
refracting goniometer invented by the late Dr. Leeson must be substituted.
With this goniometer (Fig. 109) the angles of crystals, whether microscopic
or otherwise, can be measured. It has removed the earlier difficulties
incident to similar instruments formerly in use. Among other advantages, it
is capable of measuring opaque and even imperfect crystals, beside
microscopic crystals and those in the interior of other transparent media. It is
equally applicable to the largest crystals, and will measure angles without
removing the crystal from a specimen, provided only the whole is placed on
a suitable adjusting stage. The value of the goniometer depends on the
application of a doubly refracting prism, either of Iceland spar or of quartz,
cut of such a thickness as will partially separate the two images of the angle
it is proposed to measure.
Dr. Leeson strongly insisted on the importance of the microscope in the
examination of the planes of crystals subjected to measurement, as obliquity
in many cases arises from not only conchoidal fractures, but also from
imperfect laminæ elevating one portion of a plane, and yet allowing a very
tolerable reflection when measured by the double refracting goniometer.
Microscopes for crystallographic and
petrological research are now
specially constructed for measuring
the angles of crystals.
Erector eye-pieces and erecting
prisms are employed for the purpose
of causing the image presented to the
eye to correspond with that of the Fig. 109.—Leeson’s Goniometer.
object. They are also helpful in
making minute dissections of structure; the loss of light, however, by
sending it through two additional surfaces is a drawback, and impairs the
sharpness of the image. Nachet designed an extremely ingenious
arrangement whereby the inverted image became erect; he adapted a simple
rectangular prism to the eye-piece. The obliquity which a prism gives to the
visual rays when the microscope is used in the erect position, as for
dissecting, is an advantage, as it brings the image to the eye at an angle very
Page 195
nearly corresponding to that of the inclined position in which the microscope
is ordinarily used.
The Achromatic Objective.
Fig. 110.—Pan-aplanatic Achromatic Objectives.
The Achromatic Objective, of all the optical and mechanical adjuncts to the
microscope, is in every way the most necessary, as well as the most
important. The ideal of perfection aimed at by the optician is a combination
of lenses that shall produce a perfect image—that is, one absolutely perfect
in definition and almost free from colour. The method resorted to for the
elimination of spherical and chromatic aberration in the lens has been fully
explained in a former chapter. It will now be my endeavour to show the
progressive stages of achromatism and evolution of the microscope
throughout the present century.
It is almost as difficult to assign the date of the earliest application of
achromatism to the microscope as to that of the inception and many
modifications of the instrument in past ages; indeed, the question of priority
in every step taken in its improvement has been the subject of controversy.
is ordinarily used.
The Achromatic Objective.
Fig. 110.—Pan-aplanatic Achromatic Objectives.
The Achromatic Objective, of all the optical and mechanical adjuncts to the
microscope, is in every way the most necessary, as well as the most
important. The ideal of perfection aimed at by the optician is a combination
of lenses that shall produce a perfect image—that is, one absolutely perfect
in definition and almost free from colour. The method resorted to for the
elimination of spherical and chromatic aberration in the lens has been fully
explained in a former chapter. It will now be my endeavour to show the
progressive stages of achromatism and evolution of the microscope
throughout the present century.
It is almost as difficult to assign the date of the earliest application of
achromatism to the microscope as to that of the inception and many
modifications of the instrument in past ages; indeed, the question of priority
in every step taken in its improvement has been the subject of controversy.
Page 196
Among the earlier workers in the first decade of this century will be found
the name of Bernardo Marzoni, who was curator of the Physical Laboratory
of the Lyceum of Brescia. He, an amateur optician, it has come to light, in
1808 constructed an achromatic objective, and exhibited it at Milan in 1811,
when he obtained the award of a silver medal for its merits, under the
authority of the “Institute Reale delli Scienzo.” Through the good offices of
the late Mr. John Mayall one of Marzoni’s objectives, which had been
carefully preserved, was presented to the Royal Microscopical Society of
London in 1890.20 This objective is a cemented combination, with the plane
side of the flint-lens presented to the object. This was an improvement of a
practical kind, and of which Chevalier subsequently availed himself. In 1823
Selligue, a French optician, is credited with having first suggested the plan
of combining two, three, or four plano-convex achromatic doublets of
similar foci, one above the other, to increase the power and the aperture of
the microscope. Fresnel, who reported upon this invention, preferred on the
whole Adam’s arrangement, because it gave a larger field. Selligue
subsequently improved his objective by placing a small diaphragm between
the mirror and the object.
In this country, Tully was induced by Dr. Goring to work at the achromatic
objective, and his first efforts were attended with a success quite equal to
that of Chevalier’s. Lister on examining these lenses said:—“The French
optician knows nothing of the value of aperture, but he has shown us that
fine performance is not confined to triple objectives.” Amici, the amateur
optician of Modena, visited this country in 1827 and brought his achromatic
microscope and objectives, which were seen to give increase of aperture by
combining doublets with triplets. The most lasting improvement in the
achromatic objective was that of Joseph Jackson Lister, F.R.S., the father of
Lord Lister, and one of the founders of the Royal Microscopical Society of
London.
Lister’s discoveries at this period (1829) in the history of the optics of the
microscope were of greater importance than they have been represented to
be. That he was an enthusiast is manifest, for, being unable to find an
optician to carry out his formula for grinding lenses, he at once set to work
to grind his own, and in a short time was able to make a lens which was said
to be the best of the day.
the name of Bernardo Marzoni, who was curator of the Physical Laboratory
of the Lyceum of Brescia. He, an amateur optician, it has come to light, in
1808 constructed an achromatic objective, and exhibited it at Milan in 1811,
when he obtained the award of a silver medal for its merits, under the
authority of the “Institute Reale delli Scienzo.” Through the good offices of
the late Mr. John Mayall one of Marzoni’s objectives, which had been
carefully preserved, was presented to the Royal Microscopical Society of
London in 1890.20 This objective is a cemented combination, with the plane
side of the flint-lens presented to the object. This was an improvement of a
practical kind, and of which Chevalier subsequently availed himself. In 1823
Selligue, a French optician, is credited with having first suggested the plan
of combining two, three, or four plano-convex achromatic doublets of
similar foci, one above the other, to increase the power and the aperture of
the microscope. Fresnel, who reported upon this invention, preferred on the
whole Adam’s arrangement, because it gave a larger field. Selligue
subsequently improved his objective by placing a small diaphragm between
the mirror and the object.
In this country, Tully was induced by Dr. Goring to work at the achromatic
objective, and his first efforts were attended with a success quite equal to
that of Chevalier’s. Lister on examining these lenses said:—“The French
optician knows nothing of the value of aperture, but he has shown us that
fine performance is not confined to triple objectives.” Amici, the amateur
optician of Modena, visited this country in 1827 and brought his achromatic
microscope and objectives, which were seen to give increase of aperture by
combining doublets with triplets. The most lasting improvement in the
achromatic objective was that of Joseph Jackson Lister, F.R.S., the father of
Lord Lister, and one of the founders of the Royal Microscopical Society of
London.
Lister’s discoveries at this period (1829) in the history of the optics of the
microscope were of greater importance than they have been represented to
be. That he was an enthusiast is manifest, for, being unable to find an
optician to carry out his formula for grinding lenses, he at once set to work
to grind his own, and in a short time was able to make a lens which was said
to be the best of the day.
Page 197
Lister, in a paper contributed to the proceedings of the Royal Society the
same year, pointed out how the aberrations of one doublet could be
neutralised by a second. He further demonstrated that the flint lens should be
a plano-concave joined by a permanent cement to the convex crown-glass.
The first condition, he states, “obviates the risk of error in centring the two
curves, and the second diminishes by one half the loss of light from
reflection, which is very great at the numerous surfaces of every
combination.” These two conditions then—that the flint lens shall be plano-
concave, and that it shall be joined by some cement (Canada balsam) to the
convex—may be taken as the basis for the microscopic objective, provided
they can be reconciled with the correction of spherical and chromatic
aberration of a large pencil.
Andrew Ross was not slow to perceive the value of Lister’s suggestions and
in 1831 he had constructed an object-glass on the lines laid down by Lister,
Fig. 112; a a′ representing the anterior pair, m the middle, and p the
posterior, the three sets combined forming the achromatic objective,
consisting of three pairs of lenses, a double-convex crown-glass, and a
plano-concave of flint.
Fig. 111.—Lister’s double-convex crown and plano-concave Fig. 112.—Andrew Ross’s ¼-
flint cemented combination. inch Objective.
Lister proposed other combinations, and himself made an object-glass
consisting of a meniscus pair with a triple middle, and a back plano-convex
doublet. This had a working distance of ·11 and proved to be so great a
same year, pointed out how the aberrations of one doublet could be
neutralised by a second. He further demonstrated that the flint lens should be
a plano-concave joined by a permanent cement to the convex crown-glass.
The first condition, he states, “obviates the risk of error in centring the two
curves, and the second diminishes by one half the loss of light from
reflection, which is very great at the numerous surfaces of every
combination.” These two conditions then—that the flint lens shall be plano-
concave, and that it shall be joined by some cement (Canada balsam) to the
convex—may be taken as the basis for the microscopic objective, provided
they can be reconciled with the correction of spherical and chromatic
aberration of a large pencil.
Andrew Ross was not slow to perceive the value of Lister’s suggestions and
in 1831 he had constructed an object-glass on the lines laid down by Lister,
Fig. 112; a a′ representing the anterior pair, m the middle, and p the
posterior, the three sets combined forming the achromatic objective,
consisting of three pairs of lenses, a double-convex crown-glass, and a
plano-concave of flint.
Fig. 111.—Lister’s double-convex crown and plano-concave Fig. 112.—Andrew Ross’s ¼-
flint cemented combination. inch Objective.
Lister proposed other combinations, and himself made an object-glass
consisting of a meniscus pair with a triple middle, and a back plano-convex
doublet. This had a working distance of ·11 and proved to be so great a
Page 198
success that other opticians—Hugh Powell, 1834; James Smith, 1839—
made objectives after the same formula.
The publication of Lister’s data proved of value in another direction: it
stimulated opticians to apply themselves to the further improvement of the
achromatic objective. Andrew Ross was one of the more earnest workers in
giving effect to Lister’s principles and a short time afterwards found that a
triple combination, with the lenses separated by short intervals, gave better
results. In the accompanying diagram the changes made in the combination
of the objective from 1831, and extending over a period of about twenty
years from this date, are shown.
Each objective, from the ½-inch to the 1⁄12-inch, is seen to be built up of at
least six or eight different fronts, the back combinations being a triplet
formed of two double-convex lenses of crown glass with an intermediary
double concave lens of flint-glass.
Fig. 113.—Combinations of Early Dry Objectives.
A, Double-convex lens; B, Plano-concave; C, Bi-convex and plano-concave united;
shown in their various combinations, as at D, form the 3-in., 2-in. or 1½-in.; at E,
1-in. and 2⁄3-in.; and at F, the ½-in., 4⁄10-in., ¼-in. and 1⁄25-in. objectives.
Combination D was for many years known as the Norfolk Objective.
made objectives after the same formula.
The publication of Lister’s data proved of value in another direction: it
stimulated opticians to apply themselves to the further improvement of the
achromatic objective. Andrew Ross was one of the more earnest workers in
giving effect to Lister’s principles and a short time afterwards found that a
triple combination, with the lenses separated by short intervals, gave better
results. In the accompanying diagram the changes made in the combination
of the objective from 1831, and extending over a period of about twenty
years from this date, are shown.
Each objective, from the ½-inch to the 1⁄12-inch, is seen to be built up of at
least six or eight different fronts, the back combinations being a triplet
formed of two double-convex lenses of crown glass with an intermediary
double concave lens of flint-glass.
Fig. 113.—Combinations of Early Dry Objectives.
A, Double-convex lens; B, Plano-concave; C, Bi-convex and plano-concave united;
shown in their various combinations, as at D, form the 3-in., 2-in. or 1½-in.; at E,
1-in. and 2⁄3-in.; and at F, the ½-in., 4⁄10-in., ¼-in. and 1⁄25-in. objectives.
Combination D was for many years known as the Norfolk Objective.
Page 199
No sooner had Ross constructed ¼-
inch achromatic objectives on Lister’s
formula than he discovered an error
which had hitherto escaped attention,
viz., that the thinnest cover-glass of an
object produced a considerable
amount of refractive disturbance. A
marked difference was observed in the
image when viewed with or without a
cover-glass. This difficulty was first
met by the addition of a draw-tube to Fig. 114.—Lister’s CorrectionCollar, (in section).
the microscope body. But as this also
impaired the image, Lister overcame the difficulty by mounting the front
lens of the objective in a separate tube made to fit over a second tube
carrying the two pairs of lenses. This arrangement led up to his invention of
the screw-collar adjustment, the mechanism for applying which is shown in
Fig. 114. The anterior lens a at the end of the tube is enclosed in a brass-
piece b containing the combination; the tube a, holding the lens nearest the
object, is then made to move up or down the cylinder b, thus varying the
distance, according to the thickness of the glass covering the object, by
turning the screw ring c, thus causing the one tube to slide over the other,
and clamping them together when properly adjusted. An aperture is made in
the tube a, within which is seen a mark engraved on the cylinder, on the edge
of which are two marks, a longer and a shorter, engraved upon the tube.
When the mark on the cylinder coincides with the longer mark on the tube,
the adjustment is made for an uncovered object; and when the coincidence is
with the shorter mark, the proper distance is obtained to balance the
aberrations produced by a cover-glass the hundredth of an inch thick; such
glass covers are now supplied. The adjustment should be tested
experimentally by moving the milled edge which separates or closes the
combinations, and at the same time using the fine adjusting screw of the
microscope. The difficulty associated with the cover-glass of old has, by the
introduction of the homogeneous immersion system, been very nearly
eliminated. There still remains, however, a disturbing amount of residual
colour aberration in the achromatic dry objective, and for the correction of
which Zeiss proposed mounting the several lenses on a method somewhat
different to that so long in use in this country. Fig. 115 shows an objective in
inch achromatic objectives on Lister’s
formula than he discovered an error
which had hitherto escaped attention,
viz., that the thinnest cover-glass of an
object produced a considerable
amount of refractive disturbance. A
marked difference was observed in the
image when viewed with or without a
cover-glass. This difficulty was first
met by the addition of a draw-tube to Fig. 114.—Lister’s CorrectionCollar, (in section).
the microscope body. But as this also
impaired the image, Lister overcame the difficulty by mounting the front
lens of the objective in a separate tube made to fit over a second tube
carrying the two pairs of lenses. This arrangement led up to his invention of
the screw-collar adjustment, the mechanism for applying which is shown in
Fig. 114. The anterior lens a at the end of the tube is enclosed in a brass-
piece b containing the combination; the tube a, holding the lens nearest the
object, is then made to move up or down the cylinder b, thus varying the
distance, according to the thickness of the glass covering the object, by
turning the screw ring c, thus causing the one tube to slide over the other,
and clamping them together when properly adjusted. An aperture is made in
the tube a, within which is seen a mark engraved on the cylinder, on the edge
of which are two marks, a longer and a shorter, engraved upon the tube.
When the mark on the cylinder coincides with the longer mark on the tube,
the adjustment is made for an uncovered object; and when the coincidence is
with the shorter mark, the proper distance is obtained to balance the
aberrations produced by a cover-glass the hundredth of an inch thick; such
glass covers are now supplied. The adjustment should be tested
experimentally by moving the milled edge which separates or closes the
combinations, and at the same time using the fine adjusting screw of the
microscope. The difficulty associated with the cover-glass of old has, by the
introduction of the homogeneous immersion system, been very nearly
eliminated. There still remains, however, a disturbing amount of residual
colour aberration in the achromatic dry objective, and for the correction of
which Zeiss proposed mounting the several lenses on a method somewhat
different to that so long in use in this country. Fig. 115 shows an objective in
Page 200
which the screw-collar ring b b is made to adjust the exact distance between
the two back lenses placed at a a. The value of the screw-collar is not
questioned. It is difficult to obtain at all times cover-glasses of a perfectly
uniform thickness; they will vary, and therefore perfect definition must be
obtained, as heretofore, by adjusting for each separate preparation while the
object is under examination.
As early as 1842 the excellence of
Andrew Ross’s achromatic objectives
were acknowledged, and his formula
for their construction was generally
followed. No doubt many of these early
objectives of his manufacture are still
regarded as treasures. I possess a ½-
inch and a ¼-inch, which I believe to be
comparable with any achromatic
objectives of the same apertures of the
present day. These I have always found
most serviceable for histological work.
In 1850 Mr. Wenham produced an
Fig. 115.—The Continental Screw-collar
achromatic objective of considerable
Adjustment.
achromatic value. This consisted of a
single hemispherical front combination,
shown in the accompanying enlarged diagram, Fig. 116. Wenham’s formula
seems to have been generally adopted by Continental opticians, who sold
these lenses at a reduction of price. In Paris, Prazmowski and Hartnack—I
have had one of Hartnack’s earliest immersions in use for many years—
brought this form of objective to greater perfection, and in 1867 Powell and
Lealand adopted the single front combination system in their early water-
immersion objective, whereby the focal distance was said to be “practically a
constant quantity, while reduction of aperture by making the front lens
thinner ensures a much greater working distance without affecting the
aberrations, since the first refraction takes place at the posterior or curved
surface of the front lens, the removal of any portion of thickness at the
anterior or plane surface simply cuts off zones of peripheral rays without
altering the distance—any space being filled by the homogeneous immersion
fluid, or by an extra thickness of cover-glass.”21
the two back lenses placed at a a. The value of the screw-collar is not
questioned. It is difficult to obtain at all times cover-glasses of a perfectly
uniform thickness; they will vary, and therefore perfect definition must be
obtained, as heretofore, by adjusting for each separate preparation while the
object is under examination.
As early as 1842 the excellence of
Andrew Ross’s achromatic objectives
were acknowledged, and his formula
for their construction was generally
followed. No doubt many of these early
objectives of his manufacture are still
regarded as treasures. I possess a ½-
inch and a ¼-inch, which I believe to be
comparable with any achromatic
objectives of the same apertures of the
present day. These I have always found
most serviceable for histological work.
In 1850 Mr. Wenham produced an
Fig. 115.—The Continental Screw-collar
achromatic objective of considerable
Adjustment.
achromatic value. This consisted of a
single hemispherical front combination,
shown in the accompanying enlarged diagram, Fig. 116. Wenham’s formula
seems to have been generally adopted by Continental opticians, who sold
these lenses at a reduction of price. In Paris, Prazmowski and Hartnack—I
have had one of Hartnack’s earliest immersions in use for many years—
brought this form of objective to greater perfection, and in 1867 Powell and
Lealand adopted the single front combination system in their early water-
immersion objective, whereby the focal distance was said to be “practically a
constant quantity, while reduction of aperture by making the front lens
thinner ensures a much greater working distance without affecting the
aberrations, since the first refraction takes place at the posterior or curved
surface of the front lens, the removal of any portion of thickness at the
anterior or plane surface simply cuts off zones of peripheral rays without
altering the distance—any space being filled by the homogeneous immersion
fluid, or by an extra thickness of cover-glass.”21
Page 201
Great improvements were brought
about by R. B. Tolles, of Boston,
1874, in the objective, as well as in
the optical and mechanical parts of
the microscope, most of which,
however, must be ascribed to the
criticisms and suggestions of amateur
workers skilled in the exhibition of
test-objects—the late Dr. Woodward
of Washington, for example, whose
series of photographs of the more
difficult frustules of diatoms have
rarely been surpassed. Such results
were due to improvements made in Fig. 116.—A Single Front Combination
the optical part of the microscope at formulated by Wenham for Messrs. Ross
his suggestion. He came to the (enlarged).
conclusion, arrived at about the same
time by mathematical scientists, that increase of power in the microscope
was only possible in two directions, the qualitative and the quantitative.
It was now that microscopists turned to the late Professor Abbe for
assistance in perfecting the objective in the dioptric direction. This, he
pointed out, must be looked for in further improvements in the art of glass-
making.
A series of experiments ultimately brought to light a mineral substance,
Fluorite, which, when combined in the proper proportion, one part to two of
German crown and flint glass, was found to have the qualities looked for,
and to possess different relations of a dispersive and refractive power. From
Professor Abbe’s researches, begun in 1876, we have had the aperture of the
objective greatly enlarged, and the homogeneous system brought into
general use.
Previous to this date the best made objective merely approximated to colour
correction. Undoubtedly the chief object to be obtained was the removal or
diminution of the secondary colour aberration. This, together with other
residual errors Abbe pointed out in 1880, led to the improvement of the
optical quality of the glass used in the manufacture of all optical instruments,
about by R. B. Tolles, of Boston,
1874, in the objective, as well as in
the optical and mechanical parts of
the microscope, most of which,
however, must be ascribed to the
criticisms and suggestions of amateur
workers skilled in the exhibition of
test-objects—the late Dr. Woodward
of Washington, for example, whose
series of photographs of the more
difficult frustules of diatoms have
rarely been surpassed. Such results
were due to improvements made in Fig. 116.—A Single Front Combination
the optical part of the microscope at formulated by Wenham for Messrs. Ross
his suggestion. He came to the (enlarged).
conclusion, arrived at about the same
time by mathematical scientists, that increase of power in the microscope
was only possible in two directions, the qualitative and the quantitative.
It was now that microscopists turned to the late Professor Abbe for
assistance in perfecting the objective in the dioptric direction. This, he
pointed out, must be looked for in further improvements in the art of glass-
making.
A series of experiments ultimately brought to light a mineral substance,
Fluorite, which, when combined in the proper proportion, one part to two of
German crown and flint glass, was found to have the qualities looked for,
and to possess different relations of a dispersive and refractive power. From
Professor Abbe’s researches, begun in 1876, we have had the aperture of the
objective greatly enlarged, and the homogeneous system brought into
general use.
Previous to this date the best made objective merely approximated to colour
correction. Undoubtedly the chief object to be obtained was the removal or
diminution of the secondary colour aberration. This, together with other
residual errors Abbe pointed out in 1880, led to the improvement of the
optical quality of the glass used in the manufacture of all optical instruments,
Page 202
the chief difficulties being surmounted in the Jena glass factory, whereby a
complete revolution was effected in the microscopic objective. The
apochromatic glasses of Zeiss, Powell, Beck, Ross, Watson, Swift, and other
makers, in which the secondary spectrum has been totally eliminated, or
only a negligible tertiary spectrum remains—that is to say, the objectives of
these makers—are now corrected for three spectrum rays, and not two, as in
the older objectives; and only those who look forward for making further
discoveries in the intimate structure of bacilli or for resolving the finest
diatom markings can be said to fully appreciate the importance and value of
the investigations of the late Professor Abbe, and which have, so to speak,
entirely changed old empirical views as to the value of high aperture, and
demonstrated that high amplification, unless associated by proportionally
high aperture, necessarily produces untrue images of minute structures. It
was he also who introduced a practically perfect system of estimating
apertures, known as the “numerical aperture notation,” by which not only
can an accurate comparison be made of the relative apertures of any series of
objectives, whether dry or immersion, but their resolving power under the
various conditions of the kind of light employed. Their penetrating power
and their illuminating power can now be estimated with mathematical
exactness.
The practical advantages, then,
secured by the adoption of the
homogeneous system were, on the
whole, greater than any before made
or believed to be possible, and when
taken into account in connection with
the improvement of the eye-piece
(also due to Abbe), almost perfect
achromatism and homogeneity
between objective, object, and eye-
piece is secured, together with a sharp
definition of the image over the whole
visual field. These, with an increase
Fig. 117.—Diagram of an Apochromatic
of working distance between the Combination.
object and the objective, and other
important results, have been placed within the reach of the microscopist by
men of science, and the outcome is the general adoption of the homogeneous
complete revolution was effected in the microscopic objective. The
apochromatic glasses of Zeiss, Powell, Beck, Ross, Watson, Swift, and other
makers, in which the secondary spectrum has been totally eliminated, or
only a negligible tertiary spectrum remains—that is to say, the objectives of
these makers—are now corrected for three spectrum rays, and not two, as in
the older objectives; and only those who look forward for making further
discoveries in the intimate structure of bacilli or for resolving the finest
diatom markings can be said to fully appreciate the importance and value of
the investigations of the late Professor Abbe, and which have, so to speak,
entirely changed old empirical views as to the value of high aperture, and
demonstrated that high amplification, unless associated by proportionally
high aperture, necessarily produces untrue images of minute structures. It
was he also who introduced a practically perfect system of estimating
apertures, known as the “numerical aperture notation,” by which not only
can an accurate comparison be made of the relative apertures of any series of
objectives, whether dry or immersion, but their resolving power under the
various conditions of the kind of light employed. Their penetrating power
and their illuminating power can now be estimated with mathematical
exactness.
The practical advantages, then,
secured by the adoption of the
homogeneous system were, on the
whole, greater than any before made
or believed to be possible, and when
taken into account in connection with
the improvement of the eye-piece
(also due to Abbe), almost perfect
achromatism and homogeneity
between objective, object, and eye-
piece is secured, together with a sharp
definition of the image over the whole
visual field. These, with an increase
Fig. 117.—Diagram of an Apochromatic
of working distance between the Combination.
object and the objective, and other
important results, have been placed within the reach of the microscopist by
men of science, and the outcome is the general adoption of the homogeneous
Page 203
system, termed by Carl Zeiss, a fellow-worker with Abbe, the22
apochromatic system of constructing objectives.
Relative Merits of the English and German Objectives.
As to the relative merits of German-made objectives, no superiority can be
claimed for them over those made by English opticians.
The Continental form of the 1⁄12-inch oil-immersion objective, shown in Fig.
118, on the scale of 6 to 1, consists of four systems of lenses, namely, the
front, a deep hemispherical crown lens of high refractive index; the second
front of the system, an achromatic lens of such a form that it gathers the light
from the hemispherical front; the middle lens, a single meniscus; and the
back an achromatised lens, the second front of the back being connected in
such a way as to compensate for the spherical and chromatic aberrations of
the front lens.
The first homogeneous immersion objective which came under my
observation was manufactured in the well-known Jena workshop of Carl
Zeiss, December, 1877. This had a very considerable increase of numerical
aperture, upwards of 50 per cent.; a clear gain, as an oil angle of even 110°
proved to be of greater value than an angle of 180° in air, while the resolving
power of the objective was increased in like proportion. There does not at
present appear to be a bar to the construction of objectives of yet higher
power, with increase of aperture. The available course open in this direction
is the further discovery of another vitreous material and a suitable immersion
fluid with an index of 1·8 or 1·9, and glass with a corresponding index, so as
to ensure homogeneity of the combination. Zeiss asserts that in the more
difficult departments of microscopical research the apochromatic lenses will
supplant the older objectives, yet there are many problems in microscopy
awaiting solution which do not demand the highest attainable degree of
perfection in the objective, and in the majority of cases the older achromatic
objective is all that is needful, provided it is good of its kind. The achromatic
objectives and eye-pieces of the older type have still an advantage, as, owing
to their simpler construction, really good lenses of the class required can be
purchased at considerably lower prices than the objectives of the new series.
apochromatic system of constructing objectives.
Relative Merits of the English and German Objectives.
As to the relative merits of German-made objectives, no superiority can be
claimed for them over those made by English opticians.
The Continental form of the 1⁄12-inch oil-immersion objective, shown in Fig.
118, on the scale of 6 to 1, consists of four systems of lenses, namely, the
front, a deep hemispherical crown lens of high refractive index; the second
front of the system, an achromatic lens of such a form that it gathers the light
from the hemispherical front; the middle lens, a single meniscus; and the
back an achromatised lens, the second front of the back being connected in
such a way as to compensate for the spherical and chromatic aberrations of
the front lens.
The first homogeneous immersion objective which came under my
observation was manufactured in the well-known Jena workshop of Carl
Zeiss, December, 1877. This had a very considerable increase of numerical
aperture, upwards of 50 per cent.; a clear gain, as an oil angle of even 110°
proved to be of greater value than an angle of 180° in air, while the resolving
power of the objective was increased in like proportion. There does not at
present appear to be a bar to the construction of objectives of yet higher
power, with increase of aperture. The available course open in this direction
is the further discovery of another vitreous material and a suitable immersion
fluid with an index of 1·8 or 1·9, and glass with a corresponding index, so as
to ensure homogeneity of the combination. Zeiss asserts that in the more
difficult departments of microscopical research the apochromatic lenses will
supplant the older objectives, yet there are many problems in microscopy
awaiting solution which do not demand the highest attainable degree of
perfection in the objective, and in the majority of cases the older achromatic
objective is all that is needful, provided it is good of its kind. The achromatic
objectives and eye-pieces of the older type have still an advantage, as, owing
to their simpler construction, really good lenses of the class required can be
purchased at considerably lower prices than the objectives of the new series.
Page 204
These, from being more complicated in construction, involve a greater
amount of skilled manual labour.
The German glasses of to-day
afford satisfactory evidence both
of skill and workmanship
displayed in their production.
Their cost is greater, then, for the
reason given, as will be seen on
reference to Continental
catalogues. The dry series of
objectives cost somewhat less, a
½-inch (numerical aperture 0·30)
can be had for £1 10s., and a 1⁄6-
inch (numerical aperture 0·65) for
£2. On the other hand, the
apochromatic series rapidly
increase in price as the numerical
Fig. 118.—The Continental 1⁄12-in. Oil-immersion
Combination (enlarged diagram). aperture approaches the limit of
numerical aperture 0·40. The best
of Zeiss’s series are the 12 mm. (½-inch) and the 3 mm. (1⁄8-inch), numerical
aperture 1·4, both of which possess the optical capacity assigned to them.
These objectives are undoubtedly the finest to be met with in the workshop
of any optician. Achromatic objectives of Continental manufacture have
been as much improved as those of English make by the introduction of the
newer varieties of glass, as already explained, while a new nomenclature has
sprung up in consequence. We now have semi-apochromatic and
parachromatic. The German opticians have followed Zeiss’s lead, since
almost the same series of objectives are given in the catalogues of Leitz,
Reichert, and Seibert, while the quality of both dry and immersion objectives
is found to be much the same. The low price of Reichert’s immersion
objectives should be noted, as their performance is quite perfect. A 1⁄12-inch
(numerical aperture 1·30) of Leitz’s, with which I have worked at bacteria,
has given me much satisfaction; supplied by Watson and Baker at £5. A 1⁄12-
inch dry objective by the same maker (numerical aperture 0·87) costs £3,
and a water immersion 1⁄12-inch (numerical aperture 1·10) £3 5s. Leitz
reminds me that it requires a good lens of from six to seven hundred
magnifying power for the examination of bacteria. For this reason he has
amount of skilled manual labour.
The German glasses of to-day
afford satisfactory evidence both
of skill and workmanship
displayed in their production.
Their cost is greater, then, for the
reason given, as will be seen on
reference to Continental
catalogues. The dry series of
objectives cost somewhat less, a
½-inch (numerical aperture 0·30)
can be had for £1 10s., and a 1⁄6-
inch (numerical aperture 0·65) for
£2. On the other hand, the
apochromatic series rapidly
increase in price as the numerical
Fig. 118.—The Continental 1⁄12-in. Oil-immersion
Combination (enlarged diagram). aperture approaches the limit of
numerical aperture 0·40. The best
of Zeiss’s series are the 12 mm. (½-inch) and the 3 mm. (1⁄8-inch), numerical
aperture 1·4, both of which possess the optical capacity assigned to them.
These objectives are undoubtedly the finest to be met with in the workshop
of any optician. Achromatic objectives of Continental manufacture have
been as much improved as those of English make by the introduction of the
newer varieties of glass, as already explained, while a new nomenclature has
sprung up in consequence. We now have semi-apochromatic and
parachromatic. The German opticians have followed Zeiss’s lead, since
almost the same series of objectives are given in the catalogues of Leitz,
Reichert, and Seibert, while the quality of both dry and immersion objectives
is found to be much the same. The low price of Reichert’s immersion
objectives should be noted, as their performance is quite perfect. A 1⁄12-inch
(numerical aperture 1·30) of Leitz’s, with which I have worked at bacteria,
has given me much satisfaction; supplied by Watson and Baker at £5. A 1⁄12-
inch dry objective by the same maker (numerical aperture 0·87) costs £3,
and a water immersion 1⁄12-inch (numerical aperture 1·10) £3 5s. Leitz
reminds me that it requires a good lens of from six to seven hundred
magnifying power for the examination of bacteria. For this reason he has
Page 205
constructed a new form of lens, a 1⁄10-inch oil-immersion of 2·5 mm. focus,
for the purpose of adding to the resources of bacteriology. This lens
necessarily has a lower magnification than his former 1⁄12-inch oil-lens, but as
it is less costly to manufacture it is sold at a smaller price. The before-
mentioned 1⁄12-inch, with a No. 3 compensating eye-piece, gives a
magnification of over seven hundred or eight hundred diameters. To secure
the best results in using the higher powers of Leitz’s, from No. 5 upwards, a
cover-glass of 0·17 mm. in thickness should be used, and care taken to make
the length of the draw-tube equal to 170 mm. This length of tube should be
adhered to in the use of this optician’s oil-immersion lenses. If the
microscope be provided with a nose-piece, the draw-tube should be drawn
out to 160 mm.; in its absence it should be set at 170 mm., a deviation of 10
mm. or more from the correct tube-length deteriorates from the value of
Leitz’s oil-immersion objectives as of other opticians. It is suggested that the
German apochromatic combination of three cemented lenses is that adopted
by Steinheil long before, in the construction of his well-known hand-
magnifier (see page 77, Fig. 51). Zeiss’s 3 mm. objective has a triple front,
balanced by two triple backs—in all nine lenses—a somewhat amplified
diagram of which is represented in Fig. 118. The formula for this
combination was furnished by Tolles, of Boston, America, and it at once
secured increase of aperture (the value of this optician’s many contributions
to microscopy has since his death been generally acknowledged). The
metrical equivalent focus assigned by Zeiss to his series of dry achromatic
objectives is given in somewhat ambiguous terms, which tend to confuse
rather than classify them; for instance, two lenses of the same aperture—24
mm. and 16 mm.—corresponding to the English 1-inch and 2⁄3-inch, each
have assigned to them an aperture of 0·30; a 12 mm. and 8 mm.,
corresponding to the English ½-inch and 1⁄3-inch, have an aperture of 0·65;
while a 6 mm. = ¼-inch, and a 4 mm. = ¼-inch and 1⁄6-inch, have each an
aperture of 0·95.
Nachet exhibited at the Antwerp Exhibition a fine 1⁄10-inch oil-immersion,
which was highly praised by the jurors.
It is necessary, to make the fact perfectly clear, that dry and immersion
lenses having the same angular aperture have also a similar defining power.
The pencil of rays, however, differs in intensity and density as the rays
emerging from the cover-glass of the object into air are very considerably
for the purpose of adding to the resources of bacteriology. This lens
necessarily has a lower magnification than his former 1⁄12-inch oil-lens, but as
it is less costly to manufacture it is sold at a smaller price. The before-
mentioned 1⁄12-inch, with a No. 3 compensating eye-piece, gives a
magnification of over seven hundred or eight hundred diameters. To secure
the best results in using the higher powers of Leitz’s, from No. 5 upwards, a
cover-glass of 0·17 mm. in thickness should be used, and care taken to make
the length of the draw-tube equal to 170 mm. This length of tube should be
adhered to in the use of this optician’s oil-immersion lenses. If the
microscope be provided with a nose-piece, the draw-tube should be drawn
out to 160 mm.; in its absence it should be set at 170 mm., a deviation of 10
mm. or more from the correct tube-length deteriorates from the value of
Leitz’s oil-immersion objectives as of other opticians. It is suggested that the
German apochromatic combination of three cemented lenses is that adopted
by Steinheil long before, in the construction of his well-known hand-
magnifier (see page 77, Fig. 51). Zeiss’s 3 mm. objective has a triple front,
balanced by two triple backs—in all nine lenses—a somewhat amplified
diagram of which is represented in Fig. 118. The formula for this
combination was furnished by Tolles, of Boston, America, and it at once
secured increase of aperture (the value of this optician’s many contributions
to microscopy has since his death been generally acknowledged). The
metrical equivalent focus assigned by Zeiss to his series of dry achromatic
objectives is given in somewhat ambiguous terms, which tend to confuse
rather than classify them; for instance, two lenses of the same aperture—24
mm. and 16 mm.—corresponding to the English 1-inch and 2⁄3-inch, each
have assigned to them an aperture of 0·30; a 12 mm. and 8 mm.,
corresponding to the English ½-inch and 1⁄3-inch, have an aperture of 0·65;
while a 6 mm. = ¼-inch, and a 4 mm. = ¼-inch and 1⁄6-inch, have each an
aperture of 0·95.
Nachet exhibited at the Antwerp Exhibition a fine 1⁄10-inch oil-immersion,
which was highly praised by the jurors.
It is necessary, to make the fact perfectly clear, that dry and immersion
lenses having the same angular aperture have also a similar defining power.
The pencil of rays, however, differs in intensity and density as the rays
emerging from the cover-glass of the object into air are very considerably
Page 206
deflected, and the cone suffers a corresponding loss of brightness. On this
important point, then, I believe it will prove of value to interpolate a clear
and full exposition of the change brought about by the cover-glass.
It is not difficult, then, to perceive the importance of Amici’s discovery as to
the value of a drop of water inserted between the object and the objective,
and it now seems somewhat surprising it should have been so long neglected
by opticians, since it is at once seen to diminish the reflection which takes
place in the incidence of oblique light. The film of water not only gives
increased aperture, but also greater cleanness and sharpness to the image.
The film, then, as already shown, collects the straying away of peripheral
rays of light, and sends them on to the eye-piece, and greatly assists in
rendering the image more perfect, and materially aids in the removal of
residuary secondary aberrations; while with air, or dry objectives, a certain
amount of aberration takes place, sufficient to affect the pencils on their
passage from the radiant to the medium of the front lens, adding a
considerable ratio to the total spherical aberration with the objective, which,
in the case of wide angles, increases disproportionately from the axis
outwards. This can only be corrected by a rough method of balancing; that
is, by introducing an excess of opposite aberration in the posterior lens. An
uncorrected residuum, rapidly increasing with larger apertures, is then left,
and this appears in the image amplified by the total power of the objective,
so that with a non-homogeneous medium there is a maximum angular
aperture which cannot be surpassed without undergoing a perceptible loss of
definition, provided working distance is required. If we abolish the anterior
aberration for all colours, by an immersion fluid which is equal to cover-
glass in refractive and dispersive power, the difficulty is at once overcome.
If, for instance, we have an objective of 140° in glass (= 1·25 N.A.) and water
as the immersion fluid, the aberration in front would affect a pencil of 140°.
Substituting a homogeneous medium, the same pencil, contracted to the
equivalent angle in that medium of 112°, will be admitted to the front lens
without any aberration, and may be made to emerge from the curved surface
also without any disturbing aberration, but contracted to an angle varying
from 70° to 90°. The first considerable spherical aberration of the pencil then
occurs at the anterior surface of the second lens, where the maximum
obliquity of the rays is already considerably diminished.
important point, then, I believe it will prove of value to interpolate a clear
and full exposition of the change brought about by the cover-glass.
It is not difficult, then, to perceive the importance of Amici’s discovery as to
the value of a drop of water inserted between the object and the objective,
and it now seems somewhat surprising it should have been so long neglected
by opticians, since it is at once seen to diminish the reflection which takes
place in the incidence of oblique light. The film of water not only gives
increased aperture, but also greater cleanness and sharpness to the image.
The film, then, as already shown, collects the straying away of peripheral
rays of light, and sends them on to the eye-piece, and greatly assists in
rendering the image more perfect, and materially aids in the removal of
residuary secondary aberrations; while with air, or dry objectives, a certain
amount of aberration takes place, sufficient to affect the pencils on their
passage from the radiant to the medium of the front lens, adding a
considerable ratio to the total spherical aberration with the objective, which,
in the case of wide angles, increases disproportionately from the axis
outwards. This can only be corrected by a rough method of balancing; that
is, by introducing an excess of opposite aberration in the posterior lens. An
uncorrected residuum, rapidly increasing with larger apertures, is then left,
and this appears in the image amplified by the total power of the objective,
so that with a non-homogeneous medium there is a maximum angular
aperture which cannot be surpassed without undergoing a perceptible loss of
definition, provided working distance is required. If we abolish the anterior
aberration for all colours, by an immersion fluid which is equal to cover-
glass in refractive and dispersive power, the difficulty is at once overcome.
If, for instance, we have an objective of 140° in glass (= 1·25 N.A.) and water
as the immersion fluid, the aberration in front would affect a pencil of 140°.
Substituting a homogeneous medium, the same pencil, contracted to the
equivalent angle in that medium of 112°, will be admitted to the front lens
without any aberration, and may be made to emerge from the curved surface
also without any disturbing aberration, but contracted to an angle varying
from 70° to 90°. The first considerable spherical aberration of the pencil then
occurs at the anterior surface of the second lens, where the maximum
obliquity of the rays is already considerably diminished.
Page 207
Fig. 119. Fig. 119a.
Figs. 119 and 119a will doubtless make this clearer. If the objective of 140°
works with water (Fig. 119), there would be a cone of rays extending up to
70° on both sides of the axis, and this large cone would be submitted to
spherical aberration at the front surface a. But with homogeneous
immersion Fig. 119a) the whole cone of 112° is admitted to the front lens
without any aberration, there being no refraction at the plane surface; and as
the spherical surface of the front lens is without notable spherical aberration,
the incident pencil is brought from the focus F to the conjugate focus F′, and
contracted to an angle of divergence of 70°-90° without having undergone
any spherical aberration at all.
The problem of correcting a very wide-angled objective has thus been
reduced by the homogeneous oil-immersion system, both in theory and
practice.23
Abbe’s Test-plate.
Abbe designed the test-plate (Fig. 120) for testing the spherical and
chromatic aberrations of objectives, and estimating the thickness of cover-
glasses corresponding to the most perfect correction: six glasses, having the
exact thickness marked on each, 0·09 to 0·24 mm., cemented in succession
on a slip, their lower surface silvered and engraved with parallel lines, the
contours of which form the test. These being coarsely ruled are easily
resolved by the lowest powers; yet, from the extreme thinness of the silver,
they form also a delicate test for objectives of the highest power and widest
Figs. 119 and 119a will doubtless make this clearer. If the objective of 140°
works with water (Fig. 119), there would be a cone of rays extending up to
70° on both sides of the axis, and this large cone would be submitted to
spherical aberration at the front surface a. But with homogeneous
immersion Fig. 119a) the whole cone of 112° is admitted to the front lens
without any aberration, there being no refraction at the plane surface; and as
the spherical surface of the front lens is without notable spherical aberration,
the incident pencil is brought from the focus F to the conjugate focus F′, and
contracted to an angle of divergence of 70°-90° without having undergone
any spherical aberration at all.
The problem of correcting a very wide-angled objective has thus been
reduced by the homogeneous oil-immersion system, both in theory and
practice.23
Abbe’s Test-plate.
Abbe designed the test-plate (Fig. 120) for testing the spherical and
chromatic aberrations of objectives, and estimating the thickness of cover-
glasses corresponding to the most perfect correction: six glasses, having the
exact thickness marked on each, 0·09 to 0·24 mm., cemented in succession
on a slip, their lower surface silvered and engraved with parallel lines, the
contours of which form the test. These being coarsely ruled are easily
resolved by the lowest powers; yet, from the extreme thinness of the silver,
they form also a delicate test for objectives of the highest power and widest
Page 208
aperture. The test-plate in its original size is seen in Fig. 120, with one of the
circles enlarged.
Fig. 120.—Abbe’s Test-plate for estimating thickness of glass-covers.
To examine an objective of large aperture, the discs must be focussed in
succession, observing in each case the quality of the image in the centre of
the field, and the variation produced by using, alternately, central and very
oblique illumination.
When the objective is perfectly corrected for spherical aberration, the
outlines of the lines in the centre of the field will be perfectly sharp by
oblique illumination, and without any nebulous doubling or indistinctness of
the edges. If, after exactly adjusting the objective for oblique light, central
illumination is used, no alteration of the focus should be necessary to show
the outlines with equal sharpness.
If an objective fulfils these conditions with any one of the discs, it is free
from spherical aberration when used with cover-glasses of that thickness. On
the other hand, if every disc shows nebulous doubling, or an indistinct
appearance of the edges of the line with oblique illumination, or, if the
objective requires a different focal adjustment to get equal sharpness with
central as with oblique light, the spherical correction of the objective is more
or less imperfect.
Nebulous doubling with oblique illumination indicates over-correction of the
marginal zone; indistinctness of the edges without marked nebulosity
indicates under-correction of the zone; an alteration of the focus for oblique
circles enlarged.
Fig. 120.—Abbe’s Test-plate for estimating thickness of glass-covers.
To examine an objective of large aperture, the discs must be focussed in
succession, observing in each case the quality of the image in the centre of
the field, and the variation produced by using, alternately, central and very
oblique illumination.
When the objective is perfectly corrected for spherical aberration, the
outlines of the lines in the centre of the field will be perfectly sharp by
oblique illumination, and without any nebulous doubling or indistinctness of
the edges. If, after exactly adjusting the objective for oblique light, central
illumination is used, no alteration of the focus should be necessary to show
the outlines with equal sharpness.
If an objective fulfils these conditions with any one of the discs, it is free
from spherical aberration when used with cover-glasses of that thickness. On
the other hand, if every disc shows nebulous doubling, or an indistinct
appearance of the edges of the line with oblique illumination, or, if the
objective requires a different focal adjustment to get equal sharpness with
central as with oblique light, the spherical correction of the objective is more
or less imperfect.
Nebulous doubling with oblique illumination indicates over-correction of the
marginal zone; indistinctness of the edges without marked nebulosity
indicates under-correction of the zone; an alteration of the focus for oblique
Page 209
and central illumination points to an absence of concurrent action of the
separate zones, which may be due to either an average under or over
correction, or to irregularity in the convergence of the rays.
Fig. 121.—Zeiss’s Cover-glass Gauge.
COVER-GLASS GAUGE.
Zeiss has gone a step further to lay the microscopist’s ghost of the cover-
glass. He invented a measurer (Fig. 121) whereby the precise determination
of thickness of glass-covers can be obtained. This measurement is effected
by a clip projecting from a circular box; the reading is given by an indicator
moving over a divided circle on the lid of the box. The divisions seen cut
round the circumference show 1⁄100ths of a millimeter. This ingenious gauge
measures upwards of 5 mm.
This necessary and important digression has led me away from the
consideration of the achromatic objective, and to which I shall now return.
English Immersion and Dry Objectives.
separate zones, which may be due to either an average under or over
correction, or to irregularity in the convergence of the rays.
Fig. 121.—Zeiss’s Cover-glass Gauge.
COVER-GLASS GAUGE.
Zeiss has gone a step further to lay the microscopist’s ghost of the cover-
glass. He invented a measurer (Fig. 121) whereby the precise determination
of thickness of glass-covers can be obtained. This measurement is effected
by a clip projecting from a circular box; the reading is given by an indicator
moving over a divided circle on the lid of the box. The divisions seen cut
round the circumference show 1⁄100ths of a millimeter. This ingenious gauge
measures upwards of 5 mm.
This necessary and important digression has led me away from the
consideration of the achromatic objective, and to which I shall now return.
English Immersion and Dry Objectives.
Page 210
The homogeneous immersion system met with its earliest as well as its
staunchest advocates among English opticians. Among its more energetic
supporters were Messrs. Powell and Lealand, who were the first to construct
a 1⁄8-inch immersion objective on a formula of their own, and which was
found to resolve test-objects not before capable of resolution by their dry
objectives. This encouraged them to make a 1⁄16-inch, acquired by Dr.
Woodward for the Army Medical Department, Washington, and
subsequently a 1⁄25-inch; neither of which surpassed their 1⁄8-inch in aperture,
and a new formula was tried in the construction of their first oil-immersion
objective. This had a duplex front, and two double backs; but even this did
not quite accomplish what was expected of it, and another change was
subsequently made; the anterior front combination became greater than a
hemisphere—a balloon-lens. This at once gave an increase of aperture to a
1⁄12-inch objective of 1·43 numerical aperture. After some few more trials a
more important change of the formula took place. The front lens was made
of flint-glass, and the combination took the form represented in diagram
(Fig. 122). This, on an enlarged scale, represents Powell’s 1⁄12-inch numerical
aperture 1·50. It is a homogeneous apochromatic immersion of high quality
and very flat field. It will be noticed that in this combination the four curves
of the lenses are very deep compared with those of other opticians.
Messrs. Ross have made many
important improvements and changes
in the construction of their several
series of achromatic objectives; the
calculations and formulæ for which
were made exclusively for them by
Dr. Schrœder. The list is too long to
quote, but most of these lenses are of
a high-class character, and work with
admirable precision. Among the best
of their objectives, I can commend a
1-inch of 30° and two oil-immersions,
a 1⁄8-inch of 1·20 and a 1⁄12-inch of
1·25 numerical aperture, each of
Fig. 122.—Powell and Lealand’s 1⁄12-in. Oil- which bear the highest oculars equally
immersion Objective, drawn on a scale of 6-1. well; a good test, as I have always
maintained, of excellence. Their 1⁄10-
staunchest advocates among English opticians. Among its more energetic
supporters were Messrs. Powell and Lealand, who were the first to construct
a 1⁄8-inch immersion objective on a formula of their own, and which was
found to resolve test-objects not before capable of resolution by their dry
objectives. This encouraged them to make a 1⁄16-inch, acquired by Dr.
Woodward for the Army Medical Department, Washington, and
subsequently a 1⁄25-inch; neither of which surpassed their 1⁄8-inch in aperture,
and a new formula was tried in the construction of their first oil-immersion
objective. This had a duplex front, and two double backs; but even this did
not quite accomplish what was expected of it, and another change was
subsequently made; the anterior front combination became greater than a
hemisphere—a balloon-lens. This at once gave an increase of aperture to a
1⁄12-inch objective of 1·43 numerical aperture. After some few more trials a
more important change of the formula took place. The front lens was made
of flint-glass, and the combination took the form represented in diagram
(Fig. 122). This, on an enlarged scale, represents Powell’s 1⁄12-inch numerical
aperture 1·50. It is a homogeneous apochromatic immersion of high quality
and very flat field. It will be noticed that in this combination the four curves
of the lenses are very deep compared with those of other opticians.
Messrs. Ross have made many
important improvements and changes
in the construction of their several
series of achromatic objectives; the
calculations and formulæ for which
were made exclusively for them by
Dr. Schrœder. The list is too long to
quote, but most of these lenses are of
a high-class character, and work with
admirable precision. Among the best
of their objectives, I can commend a
1-inch of 30° and two oil-immersions,
a 1⁄8-inch of 1·20 and a 1⁄12-inch of
1·25 numerical aperture, each of
Fig. 122.—Powell and Lealand’s 1⁄12-in. Oil- which bear the highest oculars equally
immersion Objective, drawn on a scale of 6-1. well; a good test, as I have always
maintained, of excellence. Their 1⁄10-
Page 211
inch has a somewhat larger aperture, and therefore shows a fine image of the
podura scale. The finish of Ross’s several series of objectives fully maintains
the high character and reputation of this old-established firm of opticians.
Messrs. R. and J. Beck have bestowed great attention upon the improvement
of their dry-objective series, much in demand for histological work,
especially among the students of city hospitals, who usually commence their
pathological work with the cheaper forms of objectives. In that case an inch
objective of about 25° air angle, a ½-inch of not less than 40°, and a ¼-inch
or 1⁄5-inch magnifying from 50 to 250 diameters, is quite sufficient for most
of their work. For bacteriological research, Messrs. Beck supply a 1⁄6-inch
immersion taken from a series, having a high aperture and a better finish at a
moderate price. Their 1⁄10-inch immersion has in my hands proved a
serviceable power for bacteriological research; it requires a good sub-stage
illuminating achromatic condenser to obtain the best results.
Messrs. Watson and Sons have much
enhanced their reputation by the
marked improvement lately brought
about in the manufacture of their
whole series of objectives. This
probably is chiefly due to the
introduction of the Jena glass into
their manufacture, and which has
enabled them to give increase of
aperture to one series in particular,
that of the para-chromatic, all of
which in consequence are of very
high quality. It is difficult to
particularise their several objectives,
the whole having special features in Fig. 123.—1⁄6-in. English Combination, largely
proportion to their magnifying used.
powers, while much care seems to
have been bestowed on them for the elimination of residual colour. A 1⁄8-inch
with correction collar is comprised of a single deep and rather thick front
lens, plano-concave flint, and double convex-crown for the middle and triple
combination for the back, the latter consisting of two crown lenses cemented
to a dense flint (Fig. 124) drawn to scale of 5-1, with lined portions intended
podura scale. The finish of Ross’s several series of objectives fully maintains
the high character and reputation of this old-established firm of opticians.
Messrs. R. and J. Beck have bestowed great attention upon the improvement
of their dry-objective series, much in demand for histological work,
especially among the students of city hospitals, who usually commence their
pathological work with the cheaper forms of objectives. In that case an inch
objective of about 25° air angle, a ½-inch of not less than 40°, and a ¼-inch
or 1⁄5-inch magnifying from 50 to 250 diameters, is quite sufficient for most
of their work. For bacteriological research, Messrs. Beck supply a 1⁄6-inch
immersion taken from a series, having a high aperture and a better finish at a
moderate price. Their 1⁄10-inch immersion has in my hands proved a
serviceable power for bacteriological research; it requires a good sub-stage
illuminating achromatic condenser to obtain the best results.
Messrs. Watson and Sons have much
enhanced their reputation by the
marked improvement lately brought
about in the manufacture of their
whole series of objectives. This
probably is chiefly due to the
introduction of the Jena glass into
their manufacture, and which has
enabled them to give increase of
aperture to one series in particular,
that of the para-chromatic, all of
which in consequence are of very
high quality. It is difficult to
particularise their several objectives,
the whole having special features in Fig. 123.—1⁄6-in. English Combination, largely
proportion to their magnifying used.
powers, while much care seems to
have been bestowed on them for the elimination of residual colour. A 1⁄8-inch
with correction collar is comprised of a single deep and rather thick front
lens, plano-concave flint, and double convex-crown for the middle and triple
combination for the back, the latter consisting of two crown lenses cemented
to a dense flint (Fig. 124) drawn to scale of 5-1, with lined portions intended
Page 212
to represent the flint, and white the crown glass lenses of the combination.
The initial magnification of this objective is 83 diameters, and the numerical
aperture ·94. This superior objective can be had for the small sum of £2.
Another remarkably useful and cheap objective, their 1-inch numerical
aperture 0·21, consists of two achromatic systems forming the front and
back with the separation between them of about half an inch, and may also
be especially recommended for students’ work.
In the accompanying diagram the lenses are drawn on too large a scale, and
therefore the distance between the two combinations should be much greater.
Among the more useful of Watson’s series, the 1-inch, the ½-inch, and the
1⁄6-inch, together with the 1⁄8-inch dry-objective, and a 1⁄9-inch, will be found
the most serviceable.
Messrs. Baker have their own series of
objectives, most of which are so very
nearly allied to those of the continental
opticians; and what has been said of
Zeiss’s and Leitz’s objectives may be
taken to apply also to Baker’s, who
have an established reputation for their
histological series, all of which are well
suited for students’ and class-room
work.
Messrs. Swift and Son have a new series
of objectives, semi-apochromatic and
pan-aplanatic, most of which are
excellent in quality and show increased
Fig. 124.—Watson’s 1⁄8-in. Objective Para-
chromatic Combination, scale 5-1. flatness of field together with that of
achromatism; the index of refraction in
each series having been correctly determined together with exact radial focal
distance, thus affording more available aperture. I may select for special
commendation their 1⁄12-inch £5 5s. homogeneous immersion objective,
which is in every way suitable for bacteriological work; its definition is very
good, as is seen in a micro-photograph of podura scale, given further on.
Their dry 1⁄6-inch can be had for £1 16s.—a marvel of cheapness. Of their
The initial magnification of this objective is 83 diameters, and the numerical
aperture ·94. This superior objective can be had for the small sum of £2.
Another remarkably useful and cheap objective, their 1-inch numerical
aperture 0·21, consists of two achromatic systems forming the front and
back with the separation between them of about half an inch, and may also
be especially recommended for students’ work.
In the accompanying diagram the lenses are drawn on too large a scale, and
therefore the distance between the two combinations should be much greater.
Among the more useful of Watson’s series, the 1-inch, the ½-inch, and the
1⁄6-inch, together with the 1⁄8-inch dry-objective, and a 1⁄9-inch, will be found
the most serviceable.
Messrs. Baker have their own series of
objectives, most of which are so very
nearly allied to those of the continental
opticians; and what has been said of
Zeiss’s and Leitz’s objectives may be
taken to apply also to Baker’s, who
have an established reputation for their
histological series, all of which are well
suited for students’ and class-room
work.
Messrs. Swift and Son have a new series
of objectives, semi-apochromatic and
pan-aplanatic, most of which are
excellent in quality and show increased
Fig. 124.—Watson’s 1⁄8-in. Objective Para-
chromatic Combination, scale 5-1. flatness of field together with that of
achromatism; the index of refraction in
each series having been correctly determined together with exact radial focal
distance, thus affording more available aperture. I may select for special
commendation their 1⁄12-inch £5 5s. homogeneous immersion objective,
which is in every way suitable for bacteriological work; its definition is very
good, as is seen in a micro-photograph of podura scale, given further on.
Their dry 1⁄6-inch can be had for £1 16s.—a marvel of cheapness. Of their
Page 213
general series the most useful for
histological work are the ½-inch, the
1⁄3-inch at £1 12s., and their 1⁄5-inch of
numerical aperture 0·87 at £3.
Mr. Pillischer, of Bond Street, has
manufactured many excellent
objectives. A fine homogeneous oil-
immersion 1⁄12-inch numerical
aperture 1·25 is worthy of special
notice; it will be found suitable for
bacteriological work; it has fine
definition with a considerable amount
of penetration.
Fig. 125.—Watson’s 1-in. Achromatic
Combination. A more intelligent idea of the
magnifying power of the objective
combined with the eye-piece will be gained by consulting the table given
below; precision in this respect has long been a desideratum with
microscopists.
Magnifying Powers of Eye-Pieces and Objectives.
A TYPICAL AND INITIAL SELECTION OF POWERS OF EYE-PIECES
CALCULATED FOR THE 10-INCH TUBE-LENGTH.
Huyghenian Eye-pieces.
Name A B C D E F
of Maker. 0 or No. 1 2 3 4 5 6
Baker 6 8 12 15 — — Diameters.
Beck, R. & J. 4 8 15 20 25 not made. "
Leitz 5 6 7 8 10 12 "
Powell & Lealand 5 7·5 10 20 40 " "
24
Reichert 2·5 3·5 4 5 6·5 " "
histological work are the ½-inch, the
1⁄3-inch at £1 12s., and their 1⁄5-inch of
numerical aperture 0·87 at £3.
Mr. Pillischer, of Bond Street, has
manufactured many excellent
objectives. A fine homogeneous oil-
immersion 1⁄12-inch numerical
aperture 1·25 is worthy of special
notice; it will be found suitable for
bacteriological work; it has fine
definition with a considerable amount
of penetration.
Fig. 125.—Watson’s 1-in. Achromatic
Combination. A more intelligent idea of the
magnifying power of the objective
combined with the eye-piece will be gained by consulting the table given
below; precision in this respect has long been a desideratum with
microscopists.
Magnifying Powers of Eye-Pieces and Objectives.
A TYPICAL AND INITIAL SELECTION OF POWERS OF EYE-PIECES
CALCULATED FOR THE 10-INCH TUBE-LENGTH.
Huyghenian Eye-pieces.
Name A B C D E F
of Maker. 0 or No. 1 2 3 4 5 6
Baker 6 8 12 15 — — Diameters.
Beck, R. & J. 4 8 15 20 25 not made. "
Leitz 5 6 7 8 10 12 "
Powell & Lealand 5 7·5 10 20 40 " "
24
Reichert 2·5 3·5 4 5 6·5 " "
Page 214
25
Ross 3 8 12½ 20 25 40 "
Swift & Son 6 9 12 15 18 21 "
Watson & Sons 4 6 8 10 12 15 "
Zeiss 3 4 5·5 7 9 not made. "
Compensating Eye-pieces for use with Apochromatic Objectives.
Zeiss 2 4 8 12 18 27 Diameters.
This may be taken as a typical set, further treated of among Eye-pieces.
Initial Powers of Objectives calculated for the 10-inch Tube-
length.
This is ascertained by dividing the distance of distinct vision 10 inches by
the focus of the objective, thus—
Focus-
4 3 2 1½ 1 2⁄3 ½ 4⁄10 ¼ 1⁄5 1⁄6 1⁄8 1⁄12
inches
Initial
magnifying 2·5 3·3 5 7·5 10 15 20 25 40 50 60 80 120 diameters.
power
A reference to the above table will at once show that the nomenclature of
objectives expresses at once the initial magnifying powers, but as makers
have great difficulty in so calculating their formulæ so as to obtain the exact
power, these figures must be taken as approximate. Thus a ¼-inch, which
should magnify 40 diameters if true to its description, might actually
magnify a little more or less.
The magnifying powers of Zeiss’s and other apochromatic objectives can be
ascertained by dividing the focal length of the objective in millimeters into
250 mm. (the distance of distinct vision), thus
Focus millimetres 24 16 12 4 3 2 1·5
Ross 3 8 12½ 20 25 40 "
Swift & Son 6 9 12 15 18 21 "
Watson & Sons 4 6 8 10 12 15 "
Zeiss 3 4 5·5 7 9 not made. "
Compensating Eye-pieces for use with Apochromatic Objectives.
Zeiss 2 4 8 12 18 27 Diameters.
This may be taken as a typical set, further treated of among Eye-pieces.
Initial Powers of Objectives calculated for the 10-inch Tube-
length.
This is ascertained by dividing the distance of distinct vision 10 inches by
the focus of the objective, thus—
Focus-
4 3 2 1½ 1 2⁄3 ½ 4⁄10 ¼ 1⁄5 1⁄6 1⁄8 1⁄12
inches
Initial
magnifying 2·5 3·3 5 7·5 10 15 20 25 40 50 60 80 120 diameters.
power
A reference to the above table will at once show that the nomenclature of
objectives expresses at once the initial magnifying powers, but as makers
have great difficulty in so calculating their formulæ so as to obtain the exact
power, these figures must be taken as approximate. Thus a ¼-inch, which
should magnify 40 diameters if true to its description, might actually
magnify a little more or less.
The magnifying powers of Zeiss’s and other apochromatic objectives can be
ascertained by dividing the focal length of the objective in millimeters into
250 mm. (the distance of distinct vision), thus
Focus millimetres 24 16 12 4 3 2 1·5
Page 215
Initial magnifying power 10·5 15·5 21 63 83 125 167 diameters.
The total magnification, when any eye-piece is working in conjunction with
an objective, is ascertained by multiplying the initial power of the objective
by that of the eye-piece.
The above calculations are all for a 10-inch tube-length. Should, however, a
shorter or longer length of body be employed, the magnification can at once
be ascertained by a proportion sum. If the magnification be 180 with 10-inch
tube-length, what would it be with a 6-inch body—10 : 6 :: 180 = 108
diameters.
Abbe designed three different forms of eye-pieces: 1, the searcher eye-piece;
2, the working eye-piece; and 3, the projecting eye-piece. The Searcher is a
negative form of low power. The working is both negative and positive, the
positive form of which is constructed on a newer principle; while the
projection is chiefly intended for microphotography, its field being small and
its definition superlatively sharp. These are severally explained among eye-
pieces.
High-Power Objectives.
Points of Importance for securing the best results with High-power
Objectives.—Always give to the body-tube of the microscope the length for
which the objective is corrected, 0·160 mm. for the short continental tube,
and 0·250 mm. for the English tube (10-inch). Employ both dry and
immersion objectives mounted for correction, commencing with a numerical
aperture of 0·75 (that is about 100° in air). If the graduation is not given in
thickness of cover-glass apply to the maker to correct this omission.
With the homogeneous oil-immersion objective it is highly necessary to
utilise all marginal pencils of light, to optically unite the upper lens of the
condenser with the preparation as well as the front lens of the objective by
means of a liquid having the same index of refraction or at least equal to that
of the immersion. Cedar Oil has been generally adopted for the purpose
mentioned, the better way of using which is as follows: place a drop on the
centre of the front objective, or on the top of the cover-glass, and then lower
The total magnification, when any eye-piece is working in conjunction with
an objective, is ascertained by multiplying the initial power of the objective
by that of the eye-piece.
The above calculations are all for a 10-inch tube-length. Should, however, a
shorter or longer length of body be employed, the magnification can at once
be ascertained by a proportion sum. If the magnification be 180 with 10-inch
tube-length, what would it be with a 6-inch body—10 : 6 :: 180 = 108
diameters.
Abbe designed three different forms of eye-pieces: 1, the searcher eye-piece;
2, the working eye-piece; and 3, the projecting eye-piece. The Searcher is a
negative form of low power. The working is both negative and positive, the
positive form of which is constructed on a newer principle; while the
projection is chiefly intended for microphotography, its field being small and
its definition superlatively sharp. These are severally explained among eye-
pieces.
High-Power Objectives.
Points of Importance for securing the best results with High-power
Objectives.—Always give to the body-tube of the microscope the length for
which the objective is corrected, 0·160 mm. for the short continental tube,
and 0·250 mm. for the English tube (10-inch). Employ both dry and
immersion objectives mounted for correction, commencing with a numerical
aperture of 0·75 (that is about 100° in air). If the graduation is not given in
thickness of cover-glass apply to the maker to correct this omission.
With the homogeneous oil-immersion objective it is highly necessary to
utilise all marginal pencils of light, to optically unite the upper lens of the
condenser with the preparation as well as the front lens of the objective by
means of a liquid having the same index of refraction or at least equal to that
of the immersion. Cedar Oil has been generally adopted for the purpose
mentioned, the better way of using which is as follows: place a drop on the
centre of the front objective, or on the top of the cover-glass, and then lower
Page 216
the objective by means of the coarse adjustment until it comes in contact
with the oil, and carefully bring into focus by the fine adjustment. If the slide
is held between the finger and thumb of one hand and moved from side to
side, while the other hand is working the fine adjustment, there can be no
danger of injuring either the objective or the specimen. Before putting the
microscope away, take a fine camel-hair brush dipped in ether, alcohol, or
methylated spirit, and carefully remove the oil from the objective and the
glass cover of the object; a soft chamois leather or cambric pocket
handkerchief will dry it off, or a piece of fine white blotting paper answers
equally well. Should the lens come accidentally into contact with the Canada
balsam, it must be very carefully removed either by ether or alcohol. The
former is by far the safest, as alcohol, if not very carefully used, quickly
dissolves out the balsam and loosens the cover-glass of the object.
Achromatic Condensers.
The Achromatic Condenser can no longer be classed among the accessories
of the microscope, since it is an absolutely indispensable part of its optical
arrangements. Its value, then, cannot be overrated, and the corrections of the
lenses which enter into the construction of the condenser should be made as
perfect as they can be made—in fact, as nearly approaching that of the
objective as it is possible to make them. It may therefore be of interest to
know something of the rise and progress of the achromatic condenser. In my
first chapter I have noticed the earlier attempts made by Dr. Wollaston,
whose experiments led him to fit to the underside of the stage of his
microscope a short tube, in which a plano-convex lens of about three-
quarters of an inch focal length was made to slide up and down (afterwards
moved up and down by two knobs); to improve definition he placed a stop
between the mirror and the lens. The stop was found to act better when
placed between the lens and the object. From this improvement Dr.
Wollaston enunciated that “the intensity of illumination will depend upon the
diameter of the illuminating lens and the proportion of the image to the
perforation, and may be regulated according to the wish of the observer.”
Dujardin in France and Tully in England were at work in the same direction.
The former a year or two later on contrived an instrument, which he termed
an eclairage, to remedy the defects of Wollaston’s, and for illuminating
with the oil, and carefully bring into focus by the fine adjustment. If the slide
is held between the finger and thumb of one hand and moved from side to
side, while the other hand is working the fine adjustment, there can be no
danger of injuring either the objective or the specimen. Before putting the
microscope away, take a fine camel-hair brush dipped in ether, alcohol, or
methylated spirit, and carefully remove the oil from the objective and the
glass cover of the object; a soft chamois leather or cambric pocket
handkerchief will dry it off, or a piece of fine white blotting paper answers
equally well. Should the lens come accidentally into contact with the Canada
balsam, it must be very carefully removed either by ether or alcohol. The
former is by far the safest, as alcohol, if not very carefully used, quickly
dissolves out the balsam and loosens the cover-glass of the object.
Achromatic Condensers.
The Achromatic Condenser can no longer be classed among the accessories
of the microscope, since it is an absolutely indispensable part of its optical
arrangements. Its value, then, cannot be overrated, and the corrections of the
lenses which enter into the construction of the condenser should be made as
perfect as they can be made—in fact, as nearly approaching that of the
objective as it is possible to make them. It may therefore be of interest to
know something of the rise and progress of the achromatic condenser. In my
first chapter I have noticed the earlier attempts made by Dr. Wollaston,
whose experiments led him to fit to the underside of the stage of his
microscope a short tube, in which a plano-convex lens of about three-
quarters of an inch focal length was made to slide up and down (afterwards
moved up and down by two knobs); to improve definition he placed a stop
between the mirror and the lens. The stop was found to act better when
placed between the lens and the object. From this improvement Dr.
Wollaston enunciated that “the intensity of illumination will depend upon the
diameter of the illuminating lens and the proportion of the image to the
perforation, and may be regulated according to the wish of the observer.”
Dujardin in France and Tully in England were at work in the same direction.
The former a year or two later on contrived an instrument, which he termed
an eclairage, to remedy the defects of Wollaston’s, and for illuminating
Page 217
objects with achromatic light. This was submitted for approval to Sir David
Brewster, who, when the use of the achromatic condenser was first
broached, used these encouraging words:—“I have no hesitation in saying
that the apparatus for illumination requires to be as perfect as the apparatus
for vision, and on this account I would recommend that the illuminating lens
should be perfectly free from chromatic and spherical aberration, and that
the greatest care be taken to exclude all extraneous light both from the object
and eye of the observer.” This far-seeing observer in optical science has
borne good fruit, and the outcome of his views is seen in the great
development and improvement of the achromatic condenser. In 1839
Andrew Ross made his first useful form of condenser, and gave rules for the
illumination of objects in an article written for the “Penny Cyclopædia.”
These, epitomised, read as follows: 1. That the illuminating cone should
equal the aperture of the objective, and no more. 2. With daylight, a white
cloud being in focus, the object has to be placed nearly at the apex of the
cone. The object is seen better sometimes above and sometimes below the
apex of the cone. 3. With lamplight a bull’s-eye lens is to be used, to
parallelise the rays, so that they may be similar to those coming from the
white cloud. It has been seen that Mr. Lister foreshadowed the sub-stage
condenser.
The early form of Ross’s condenser consists of two small brass tubes made
to slide one in the other. To the outer one is attached a flat brass plate which
slides underneath the stage of the microscope, and by means of a screw the
adjustment of the axis of the illuminator is effected. The upper portion of the
apparatus carries the achromatic combination, which by a rack and pinion
movement is brought nearer to, or removed further from the object on the
stage. The several parts of the illuminator unscrew, so that the lenses may be
used either combined for high powers, or separated for low powers.
Messrs. Smith & Beck greatly improved upon Ross’s condenser by adding
another achromatic lens to the combination, three being employed when
used with high-power objectives and two or even one with the lower, the
adjustment and focussing being made by rack and pinion arrangement
beneath the stage. Some further changes for the better were made in the
condenser by Powell, and in 1850 an amateur microscopist, Mr. Gillett, fully
grasping the value of controlling the cone of rays passing into the
microscope, devised a new form of condenser, in connection with which a
Brewster, who, when the use of the achromatic condenser was first
broached, used these encouraging words:—“I have no hesitation in saying
that the apparatus for illumination requires to be as perfect as the apparatus
for vision, and on this account I would recommend that the illuminating lens
should be perfectly free from chromatic and spherical aberration, and that
the greatest care be taken to exclude all extraneous light both from the object
and eye of the observer.” This far-seeing observer in optical science has
borne good fruit, and the outcome of his views is seen in the great
development and improvement of the achromatic condenser. In 1839
Andrew Ross made his first useful form of condenser, and gave rules for the
illumination of objects in an article written for the “Penny Cyclopædia.”
These, epitomised, read as follows: 1. That the illuminating cone should
equal the aperture of the objective, and no more. 2. With daylight, a white
cloud being in focus, the object has to be placed nearly at the apex of the
cone. The object is seen better sometimes above and sometimes below the
apex of the cone. 3. With lamplight a bull’s-eye lens is to be used, to
parallelise the rays, so that they may be similar to those coming from the
white cloud. It has been seen that Mr. Lister foreshadowed the sub-stage
condenser.
The early form of Ross’s condenser consists of two small brass tubes made
to slide one in the other. To the outer one is attached a flat brass plate which
slides underneath the stage of the microscope, and by means of a screw the
adjustment of the axis of the illuminator is effected. The upper portion of the
apparatus carries the achromatic combination, which by a rack and pinion
movement is brought nearer to, or removed further from the object on the
stage. The several parts of the illuminator unscrew, so that the lenses may be
used either combined for high powers, or separated for low powers.
Messrs. Smith & Beck greatly improved upon Ross’s condenser by adding
another achromatic lens to the combination, three being employed when
used with high-power objectives and two or even one with the lower, the
adjustment and focussing being made by rack and pinion arrangement
beneath the stage. Some further changes for the better were made in the
condenser by Powell, and in 1850 an amateur microscopist, Mr. Gillett, fully
grasping the value of controlling the cone of rays passing into the
microscope, devised a new form of condenser, in connection with which a
Page 218
revolving series of diaphragms of
different values were made to pass
between the achromatic lenses and the
source of light.
Andrew Ross constructed the first
condenser on Gillett’s principle, and
this proved to be one of the most
successful pieces of apparatus
contrived. Gillett’s Condenser
consists of an achromatic lens c,
about equal to an object-glass of one
quarter of an inch focal length, with
an aperture of 80°. This lens is
Fig. 126.—Original form of Gillett’s Achromatic
screwed into the top of a brass tube, Condenser.
and intersecting which, at an angle of
about 25°, is a circular rotating brass plate a b, provided with a conical
diaphragm, having a series of circular apertures of different sizes h g, each
of which in succession, as the diaphragm is rotated, proportionally limits the
light transmitted through the illuminating lens. The circular plate in which
the conical diaphragm is fixed is provided with a spring and catch e f, the
latter indicating when an aperture is central with the illuminating lens, also
the number of the aperture as marked on the graduated circular plate. Three
of these apertures have central discs for circularly oblique illumination,
allowing only the passage of a hollow cone of light to illuminate the object.
The illuminator above described is placed in the secondary stage i i, which is
situated below the general stage of the microscope, and consists of a
cylindrical tube having a rotatory motion, also a rectangular adjustment,
which is effected by means of two screws l m, one in front, and the other on
the left side of its frame. This tube receives and supports all the various
illuminating and polarising apparatus, and other auxiliaries.
Directions for using Gillett’s Condenser.—In the adjustment of the
compound body of the microscope for using with Gillett’s illuminator, one
or two important points should be observed—first, centricity; and secondly,
the fittest compensation of the light to be employed. With regard to the first,
place the illuminator in the cylindrical tube, and press upwards the sliding
bar k in its place, until checked by the stop; move the microscope body
different values were made to pass
between the achromatic lenses and the
source of light.
Andrew Ross constructed the first
condenser on Gillett’s principle, and
this proved to be one of the most
successful pieces of apparatus
contrived. Gillett’s Condenser
consists of an achromatic lens c,
about equal to an object-glass of one
quarter of an inch focal length, with
an aperture of 80°. This lens is
Fig. 126.—Original form of Gillett’s Achromatic
screwed into the top of a brass tube, Condenser.
and intersecting which, at an angle of
about 25°, is a circular rotating brass plate a b, provided with a conical
diaphragm, having a series of circular apertures of different sizes h g, each
of which in succession, as the diaphragm is rotated, proportionally limits the
light transmitted through the illuminating lens. The circular plate in which
the conical diaphragm is fixed is provided with a spring and catch e f, the
latter indicating when an aperture is central with the illuminating lens, also
the number of the aperture as marked on the graduated circular plate. Three
of these apertures have central discs for circularly oblique illumination,
allowing only the passage of a hollow cone of light to illuminate the object.
The illuminator above described is placed in the secondary stage i i, which is
situated below the general stage of the microscope, and consists of a
cylindrical tube having a rotatory motion, also a rectangular adjustment,
which is effected by means of two screws l m, one in front, and the other on
the left side of its frame. This tube receives and supports all the various
illuminating and polarising apparatus, and other auxiliaries.
Directions for using Gillett’s Condenser.—In the adjustment of the
compound body of the microscope for using with Gillett’s illuminator, one
or two important points should be observed—first, centricity; and secondly,
the fittest compensation of the light to be employed. With regard to the first,
place the illuminator in the cylindrical tube, and press upwards the sliding
bar k in its place, until checked by the stop; move the microscope body
Page 219
either vertically or inclined for convenient use; and, with the rack and pinion
which regulates the sliding bar, bring the illuminating lens to a level with the
upper surface of the object-stage; then move the arm which holds the
microscope body to the right, until it meets the stop, whereby its central
position is attained; adjust the reflecting mirror so as to throw light up the
illuminator, and place upon the mirror a piece of clean white paper to obtain
a uniform disc of light. Then put on the low eye-piece, and a low power (the
half-inch), as more convenient for the mere adjustment of the instrument;
place a transparent object on the stage, adjust the microscope-tube, until
vision is obtained of the object; then remove the object, and take off the cap
of the eye-piece, and in its place fix on the eye-glass called the “centring
eye-glass,”26 which will be found greatly to facilitate the adjustment now
under consideration, namely, the centring of the compound body of the
microscope with the illuminating apparatus of whatever description. The
centring-glass, being thus affixed to the top of the eye-piece, is adjusted by
its sliding-tube (without disturbing the microscope-tube) until the images of
the diaphragms in the object-glass and centring lens are distinctly seen. The
illuminator should now be moved by means of the left-hand screw on the
secondary stage while looking through the microscope, to enable the
observer to recognize the diaphragm belonging to the illuminator, and by
means of the two adjusting screws to place this diaphragm central with the
others: thus the first condition, that of centricity, will be accomplished.
Remove the white paper from the mirror, and also the centring-glass, and
replace the cap on the eye-piece, also the object on the stage, of which
distinct vision should then be obtained by the rack and pinion, or fine screw
adjustment, should it have become deranged.
The re-publication of the original directions is given with the view of
showing what a clear conception Gillett had of the value of his invention.
The careful directions given for centring must be regarded with interest,
although nearly superseded by the centring screw arrangement in connection
with the sub-stage. The best results, he goes on to say, will be secured by
using the plain mirror and focussing the window-bar on the object, while a
white-cloud illuminator will afford as much light as may be required. It is a
mistake to suppose that direct light is more critical than indirect. As a rule,
the student is given to over-illuminate the object. These questions will,
however, be discussed further on.
which regulates the sliding bar, bring the illuminating lens to a level with the
upper surface of the object-stage; then move the arm which holds the
microscope body to the right, until it meets the stop, whereby its central
position is attained; adjust the reflecting mirror so as to throw light up the
illuminator, and place upon the mirror a piece of clean white paper to obtain
a uniform disc of light. Then put on the low eye-piece, and a low power (the
half-inch), as more convenient for the mere adjustment of the instrument;
place a transparent object on the stage, adjust the microscope-tube, until
vision is obtained of the object; then remove the object, and take off the cap
of the eye-piece, and in its place fix on the eye-glass called the “centring
eye-glass,”26 which will be found greatly to facilitate the adjustment now
under consideration, namely, the centring of the compound body of the
microscope with the illuminating apparatus of whatever description. The
centring-glass, being thus affixed to the top of the eye-piece, is adjusted by
its sliding-tube (without disturbing the microscope-tube) until the images of
the diaphragms in the object-glass and centring lens are distinctly seen. The
illuminator should now be moved by means of the left-hand screw on the
secondary stage while looking through the microscope, to enable the
observer to recognize the diaphragm belonging to the illuminator, and by
means of the two adjusting screws to place this diaphragm central with the
others: thus the first condition, that of centricity, will be accomplished.
Remove the white paper from the mirror, and also the centring-glass, and
replace the cap on the eye-piece, also the object on the stage, of which
distinct vision should then be obtained by the rack and pinion, or fine screw
adjustment, should it have become deranged.
The re-publication of the original directions is given with the view of
showing what a clear conception Gillett had of the value of his invention.
The careful directions given for centring must be regarded with interest,
although nearly superseded by the centring screw arrangement in connection
with the sub-stage. The best results, he goes on to say, will be secured by
using the plain mirror and focussing the window-bar on the object, while a
white-cloud illuminator will afford as much light as may be required. It is a
mistake to suppose that direct light is more critical than indirect. As a rule,
the student is given to over-illuminate the object. These questions will,
however, be discussed further on.
Page 220
Very many modifications of Gillett’s
condenser have, since 1850, become
known to microscopists. Ross’s
present improved form (Fig. 127) is
made to drop into the sub-stage of the
microscope, and when adjusted, is an
extremely efficient instrument. The
optical part is similar to a 4⁄10-inch
objective. It has two sets of revolving
diaphragms, with apertures and stops
for showing surface markings in a
perfect manner.
Fig. 127.—The Ross Improved Achromatic
Condenser, with diaphragm stops.
Abbe’s Condenser.
The essential feature of this condenser is its short focus, which collects the
light reflected by the mirror, so as to form a cone of rays of very large
aperture, having its focus in the plane of the object.
condenser have, since 1850, become
known to microscopists. Ross’s
present improved form (Fig. 127) is
made to drop into the sub-stage of the
microscope, and when adjusted, is an
extremely efficient instrument. The
optical part is similar to a 4⁄10-inch
objective. It has two sets of revolving
diaphragms, with apertures and stops
for showing surface markings in a
perfect manner.
Fig. 127.—The Ross Improved Achromatic
Condenser, with diaphragm stops.
Abbe’s Condenser.
The essential feature of this condenser is its short focus, which collects the
light reflected by the mirror, so as to form a cone of rays of very large
aperture, having its focus in the plane of the object.
Page 221
The full aperture of the illuminating
cone should only be used when
finely granular and deeply stained
particles (protoplasm, bacteria, &c.)
are being examined with objectives
of large aperture. In all cases the
cone must be suitably reduced, either
by an iris, or other form of
diaphragm (central illumination). By
placing the diaphragm excentrically,
by means of rack-work attached to
Fig. 128.—The Iris Diaphragm, and carrier for the carrier, the central rays are
Stops.
excluded and a certain extra-axial
portion of the illuminating pencil
falls upon the object (oblique illumination). When the diaphragm is thus
excentrically placed, this oblique pencil can be directed from all sides by
rotating the carrier round the optic axis. The central stop diaphragm shuts
off all the axial and transmits only the marginal rays, thus producing dark-
ground illumination. The iris diaphragm (Fig. 128) is so shaped that the
edge of its smallest opening closely approximates the object-slide on the
stage.
The Abbe condenser is the most
popular form in use, for all purposes.
Owing to the large aperture of the
cone of light which it projects, it can
be employed with the highest
powers; by removing the top lens it
can also be used with low powers.
Dark ground illumination may be
obtained with it up to a ¼-inch
objective.
cone should only be used when
finely granular and deeply stained
particles (protoplasm, bacteria, &c.)
are being examined with objectives
of large aperture. In all cases the
cone must be suitably reduced, either
by an iris, or other form of
diaphragm (central illumination). By
placing the diaphragm excentrically,
by means of rack-work attached to
Fig. 128.—The Iris Diaphragm, and carrier for the carrier, the central rays are
Stops.
excluded and a certain extra-axial
portion of the illuminating pencil
falls upon the object (oblique illumination). When the diaphragm is thus
excentrically placed, this oblique pencil can be directed from all sides by
rotating the carrier round the optic axis. The central stop diaphragm shuts
off all the axial and transmits only the marginal rays, thus producing dark-
ground illumination. The iris diaphragm (Fig. 128) is so shaped that the
edge of its smallest opening closely approximates the object-slide on the
stage.
The Abbe condenser is the most
popular form in use, for all purposes.
Owing to the large aperture of the
cone of light which it projects, it can
be employed with the highest
powers; by removing the top lens it
can also be used with low powers.
Dark ground illumination may be
obtained with it up to a ¼-inch
objective.
Page 222
Fig. 129.—The Abbe Condenser, detached from
the Sub-stage of the Microscope.
Fig. 130.—Optical Arrangement of Abbe Fig. 131.—Optical Arrangement of Abbe
Illuminator, 1·2 N.A. Illuminator, 1·4 N.A.
The condenser is made in two forms of 1·2 and 1·4 numerical aperture by
Messrs. Watson. The lenses are mounted in aluminium. Fig. 130 is in more
general use, but by workers with high powers Fig. 131 is preferred, as it
ensures the most oblique illumination with objectives of largest aperture. It
is preferred for photo-micrographic purposes.
Watson’s Achromatic Condenser (Fig.
132), 1·0 numerical aperture, shown in
section, although originally designed
for use with the micro-spectroscope, is
equally efficient for ordinary purposes.
This condenser transmits a larger
aplanatic cone of light than Abbe’s. It
may therefore be employed with
higher power objectives, and by
removing the top lens it is just as
Fig. 132.—The Optical Arrangement of
Watson’s Achromatic Condenser.
useful a condenser for lower powers.
Being constructed with lenses of an
unusually large size, it is well adapted for use with the micro-spectroscope.
It is certainly one of the best all-round condensers in use. The new Schott
glass enters into the construction of the lenses, and these are mounted in
aluminium.
the Sub-stage of the Microscope.
Fig. 130.—Optical Arrangement of Abbe Fig. 131.—Optical Arrangement of Abbe
Illuminator, 1·2 N.A. Illuminator, 1·4 N.A.
The condenser is made in two forms of 1·2 and 1·4 numerical aperture by
Messrs. Watson. The lenses are mounted in aluminium. Fig. 130 is in more
general use, but by workers with high powers Fig. 131 is preferred, as it
ensures the most oblique illumination with objectives of largest aperture. It
is preferred for photo-micrographic purposes.
Watson’s Achromatic Condenser (Fig.
132), 1·0 numerical aperture, shown in
section, although originally designed
for use with the micro-spectroscope, is
equally efficient for ordinary purposes.
This condenser transmits a larger
aplanatic cone of light than Abbe’s. It
may therefore be employed with
higher power objectives, and by
removing the top lens it is just as
Fig. 132.—The Optical Arrangement of
Watson’s Achromatic Condenser.
useful a condenser for lower powers.
Being constructed with lenses of an
unusually large size, it is well adapted for use with the micro-spectroscope.
It is certainly one of the best all-round condensers in use. The new Schott
glass enters into the construction of the lenses, and these are mounted in
aluminium.
Page 223
Fig. 133.—Powell’s Achromatic Condenser.
Many microscopists consider on the whole that Powell’s sub-stage
apochromatic condenser with collar correction (Fig. 133) surpasses that of
Abbe. The mechanical arrangement of Powell’s is very simple: the
correction collar is similar to that of an ordinary objective, it has a steeper
spiral slot and only half a revolution of movement; a long arc is fixed to the
collar so that it may conveniently be reached by the finger. It is so
constructed as to turn easily and smoothly at the slightest touch. The collar
moves only the back lens of the combination, leaving the mount rigid. The
diaphragms are regulated by A and B.
Many microscopists consider on the whole that Powell’s sub-stage
apochromatic condenser with collar correction (Fig. 133) surpasses that of
Abbe. The mechanical arrangement of Powell’s is very simple: the
correction collar is similar to that of an ordinary objective, it has a steeper
spiral slot and only half a revolution of movement; a long arc is fixed to the
collar so that it may conveniently be reached by the finger. It is so
constructed as to turn easily and smoothly at the slightest touch. The collar
moves only the back lens of the combination, leaving the mount rigid. The
diaphragms are regulated by A and B.
Page 224
Fig. 134. Fig. 134a.
Fig. 134b.—Powell’s Apochromatic Oil Immersion Condenser, N.A. 1·40.
The object of the correctional movement is to increase the maximum
aplanatic aperture of the condenser by separating the lenses. If the back of a
wide-angled objective be examined when an object is illuminated by the
full aperture of the condenser, the edge of the flame being in focus, it will
be noticed that the illuminated portion of the back lens will be oval and
pointed instead of circular. Also that when the condenser is racked up,
although the external shape of the illuminated portion becomes more
circular, two dark patches will appear on either side of the centre, showing
the operation of the spherical aberration of the condenser. If under these
circumstances the lenses are separated by means of the collar adjustment,
the black spots will be closed up, and a circular and evenly-illuminated disc
of illumination of a larger size will result. The wheel of diaphragms, or a
series of graduated diaphragm discs to drop into a holder, is intended for
critical work; the diaphragm can always be recorded, and the identical
illuminating cone reproduced.
Fig. 134b.—Powell’s Apochromatic Oil Immersion Condenser, N.A. 1·40.
The object of the correctional movement is to increase the maximum
aplanatic aperture of the condenser by separating the lenses. If the back of a
wide-angled objective be examined when an object is illuminated by the
full aperture of the condenser, the edge of the flame being in focus, it will
be noticed that the illuminated portion of the back lens will be oval and
pointed instead of circular. Also that when the condenser is racked up,
although the external shape of the illuminated portion becomes more
circular, two dark patches will appear on either side of the centre, showing
the operation of the spherical aberration of the condenser. If under these
circumstances the lenses are separated by means of the collar adjustment,
the black spots will be closed up, and a circular and evenly-illuminated disc
of illumination of a larger size will result. The wheel of diaphragms, or a
series of graduated diaphragm discs to drop into a holder, is intended for
critical work; the diaphragm can always be recorded, and the identical
illuminating cone reproduced.
Page 225
Hence we have a simple method of graduating apertures between any two
contiguous diaphragms; if, for example, we place the lever to the left, so
that the lens may be separated as far as possible, and use a No. 6
diaphragm, and if, on examining the object, it is thought that the
illuminating cone is not large enough, and if when No. 7 is turned on it is
found too much, we can go back to No. 6, and by turning the lever 60°
towards the right, closing the lenses and increasing the power a little, we
shall obtain an aperture somewhere between Nos. 6 and 7 diaphragm. Thus
we can by means of the correction collar graduate the aperture with the
facility as with an iris, and we can record any particular aperture with a
degree of accuracy foreign to the iris. It must be admitted, however, that the
cone of light transmitted by the condenser is a very small one.
Powell also supplies an apochromatic oil-immersion condenser, numerical
aperture 1·40, but without collar correction; Fig. 134 shows the sliding tube
lowered by arm A and cell B withdrawn for changing stops, which can be
done without altering the focus of the condenser. Fig. 134a shows the cell B
closed and raised by arm A close to the back lens of optical combination. In
Fig. 134b six of the principal stops are shown. Powell’s dry apochromatic
condenser, of nearly 0·9 aplanatic cone, is also very good; but the high price
of all is a bar to their more general use. The speciality of these is the
conversion of axis light into condensed oblique incident light by the
refraction of the condenser.
Messrs. R. & J. Beck have various forms of achromatic condensers, some
of which partake of a somewhat elaborate arrangement; others are simple
and inexpensive, to suit the students’ microscope; as when the light of the
concave mirror proves insufficient for any object requiring intense
transmitted light, an achromatic condenser must be adapted to even the
students’ form of microscope. The latest form of condenser (Fig. 135) is
fitted with revolving stops and iris diaphragm, and other appliances for
obtaining satisfactory results.
Beck’s Compound Illuminating Apparatus (Fig. 136).—It is useful in
working with the microscope to be enabled to rapidly change the
illumination, and for this reason this compound form of condenser has been
constructed. It consists of an upper portion A, a wide-angle condenser, the
contiguous diaphragms; if, for example, we place the lever to the left, so
that the lens may be separated as far as possible, and use a No. 6
diaphragm, and if, on examining the object, it is thought that the
illuminating cone is not large enough, and if when No. 7 is turned on it is
found too much, we can go back to No. 6, and by turning the lever 60°
towards the right, closing the lenses and increasing the power a little, we
shall obtain an aperture somewhere between Nos. 6 and 7 diaphragm. Thus
we can by means of the correction collar graduate the aperture with the
facility as with an iris, and we can record any particular aperture with a
degree of accuracy foreign to the iris. It must be admitted, however, that the
cone of light transmitted by the condenser is a very small one.
Powell also supplies an apochromatic oil-immersion condenser, numerical
aperture 1·40, but without collar correction; Fig. 134 shows the sliding tube
lowered by arm A and cell B withdrawn for changing stops, which can be
done without altering the focus of the condenser. Fig. 134a shows the cell B
closed and raised by arm A close to the back lens of optical combination. In
Fig. 134b six of the principal stops are shown. Powell’s dry apochromatic
condenser, of nearly 0·9 aplanatic cone, is also very good; but the high price
of all is a bar to their more general use. The speciality of these is the
conversion of axis light into condensed oblique incident light by the
refraction of the condenser.
Messrs. R. & J. Beck have various forms of achromatic condensers, some
of which partake of a somewhat elaborate arrangement; others are simple
and inexpensive, to suit the students’ microscope; as when the light of the
concave mirror proves insufficient for any object requiring intense
transmitted light, an achromatic condenser must be adapted to even the
students’ form of microscope. The latest form of condenser (Fig. 135) is
fitted with revolving stops and iris diaphragm, and other appliances for
obtaining satisfactory results.
Beck’s Compound Illuminating Apparatus (Fig. 136).—It is useful in
working with the microscope to be enabled to rapidly change the
illumination, and for this reason this compound form of condenser has been
constructed. It consists of an upper portion A, a wide-angle condenser, the
Page 226
aperture of which can be reduced at
will by an iris diaphragm, moved by
the lever B. This can be used for all
other purposes. Below this diaphragm
is a plate C, which can be swung back
out of position at will, as shown in
outline. Into a cell in this plate the
stops D can be dropped, and the
condenser can be used for dark field
illumination, or for high powers as an
oblique illuminator. A large-size
polarising prism E, fastens to the plate
Fig. 135.—Beck’s newer form of Achromatic
Condenser. C, and can be removed when not
required. In this way any of the various
modes of illumination may be separately or conjointly obtained.
Fig. 136.—Beck’s Compound Condenser.
Their condenser (Fig. 137) has a large aperture, and facilities for rotating
the series of diaphragms. It is available for either dry or immersion
objectives up to 1·3 numerical aperture on diatoms, and wet or dry
histological objects. The spherical form of the front is worked by a milled-
head that rotates a series of lenses and diaphragms. It also avoids the
inconvenience of having the connecting fluid drawn away by capillary
will by an iris diaphragm, moved by
the lever B. This can be used for all
other purposes. Below this diaphragm
is a plate C, which can be swung back
out of position at will, as shown in
outline. Into a cell in this plate the
stops D can be dropped, and the
condenser can be used for dark field
illumination, or for high powers as an
oblique illuminator. A large-size
polarising prism E, fastens to the plate
Fig. 135.—Beck’s newer form of Achromatic
Condenser. C, and can be removed when not
required. In this way any of the various
modes of illumination may be separately or conjointly obtained.
Fig. 136.—Beck’s Compound Condenser.
Their condenser (Fig. 137) has a large aperture, and facilities for rotating
the series of diaphragms. It is available for either dry or immersion
objectives up to 1·3 numerical aperture on diatoms, and wet or dry
histological objects. The spherical form of the front is worked by a milled-
head that rotates a series of lenses and diaphragms. It also avoids the
inconvenience of having the connecting fluid drawn away by capillary
Page 227
attraction, as would be the case if
mounted on a flat surface. It is also
less in the way of the sub-stage
movements.
Fig. 137.—Beck’s Spherical Achromatic
Condenser.
Fig. 138.—Watson’s Parachromatic Condenser.
The Parachromatic Condenser of Messrs. Watson (Fig. 138) was made to
meet a demand for a condenser giving a large solid cone of illumination
free from colour. The optical part of this condenser consists of a full
hemispherical front lens, and the middle and back combinations of such
forms as to produce the necessary corrections. The Jena phosphate crown
and silicate flints are used in its manufacture, and to these are due its special
qualities. The total aperture of the condenser is 1·0, and it yields an
aplanatic aperture of ·90 numerical aperture. The magnifying power is 2⁄7ths
mounted on a flat surface. It is also
less in the way of the sub-stage
movements.
Fig. 137.—Beck’s Spherical Achromatic
Condenser.
Fig. 138.—Watson’s Parachromatic Condenser.
The Parachromatic Condenser of Messrs. Watson (Fig. 138) was made to
meet a demand for a condenser giving a large solid cone of illumination
free from colour. The optical part of this condenser consists of a full
hemispherical front lens, and the middle and back combinations of such
forms as to produce the necessary corrections. The Jena phosphate crown
and silicate flints are used in its manufacture, and to these are due its special
qualities. The total aperture of the condenser is 1·0, and it yields an
aplanatic aperture of ·90 numerical aperture. The magnifying power is 2⁄7ths
Page 228
of an inch. From this it will be seen that it is especially suitable for use with
high-power objectives.
It can also be employed without the front lens, when the magnifying power
is 4⁄10ths of an inch, and the numerical aperture ·35. It is mounted in an
exceedingly convenient manner, the iris diaphragm being fitted in such a
way as to be absolutely central with the optical system.
The arc through which the handle controlling the iris travels is divided, and
indicates the aperture at which the condenser may be working at any time.
An important feature in this condenser is that it is almost wholly free from
colour. As a rule condensers of the same form are found difficult to work
with, because of the small diameter of the field or back lens. This difficulty
has been successfully overcome by increasing the size of this lens, and the
whole of which is fully utilised.
Most London opticians have their own especial form of achromatic
condenser, designed for and fitted to their several stands and objectives,
varying from a small price to the more expensively-fitted accessories.
high-power objectives.
It can also be employed without the front lens, when the magnifying power
is 4⁄10ths of an inch, and the numerical aperture ·35. It is mounted in an
exceedingly convenient manner, the iris diaphragm being fitted in such a
way as to be absolutely central with the optical system.
The arc through which the handle controlling the iris travels is divided, and
indicates the aperture at which the condenser may be working at any time.
An important feature in this condenser is that it is almost wholly free from
colour. As a rule condensers of the same form are found difficult to work
with, because of the small diameter of the field or back lens. This difficulty
has been successfully overcome by increasing the size of this lens, and the
whole of which is fully utilised.
Most London opticians have their own especial form of achromatic
condenser, designed for and fitted to their several stands and objectives,
varying from a small price to the more expensively-fitted accessories.
Page 229
Fig. 139.—Swift’s Illuminating Polarising Apparatus.
Fig. 139a.—Swift’s Diaphragms and Central Stops.
Messrs. Swift’s illuminating apparatus (Fig. 139) is conveniently supplied
with numerous useful appliances. The optical combination A is computed to
be used as an effective spot lens from a 3-inch objective up to a sixth. C C
are two small milled heads by means of which the optical combination A is
centred to the axis of the objective. The revolving diaphragm E has four
apertures for the purpose of receiving central stops, oblique light discs, and
selenite films. D is a frame carrying two revolving cells, into one of which a
mica film is placed, which can be revolved with ease over either of the
selenites below, whereby changes of colour can be obtained in
experimenting with polarised light. The darts and P A’s indicate the position
of the positive axis of the mica and selenite films, and by this means results
can be recorded, etc. Either of the revolving cells can be thrown into the
centre of the condenser, and there stopped by means of a spring catch; when
so arranged the mica film, &c., may be revolved in its place by turning the
cell D, as both cells are geared together with fine racked teeth. F is a
polarising prism mounted on an eccentric arm, rendered central when in
use, or thrown out, as seen, when out of use. G is the rack dove-tail slide for
indicating and focussing the condenser on the object. The advantages
associated with this condenser consist in having the polarising prism,
selenite films, dark-ground, and oblique light stops, so that they may be
brought close under the optical combination.
Fig. 139a.—Swift’s Diaphragms and Central Stops.
Messrs. Swift’s illuminating apparatus (Fig. 139) is conveniently supplied
with numerous useful appliances. The optical combination A is computed to
be used as an effective spot lens from a 3-inch objective up to a sixth. C C
are two small milled heads by means of which the optical combination A is
centred to the axis of the objective. The revolving diaphragm E has four
apertures for the purpose of receiving central stops, oblique light discs, and
selenite films. D is a frame carrying two revolving cells, into one of which a
mica film is placed, which can be revolved with ease over either of the
selenites below, whereby changes of colour can be obtained in
experimenting with polarised light. The darts and P A’s indicate the position
of the positive axis of the mica and selenite films, and by this means results
can be recorded, etc. Either of the revolving cells can be thrown into the
centre of the condenser, and there stopped by means of a spring catch; when
so arranged the mica film, &c., may be revolved in its place by turning the
cell D, as both cells are geared together with fine racked teeth. F is a
polarising prism mounted on an eccentric arm, rendered central when in
use, or thrown out, as seen, when out of use. G is the rack dove-tail slide for
indicating and focussing the condenser on the object. The advantages
associated with this condenser consist in having the polarising prism,
selenite films, dark-ground, and oblique light stops, so that they may be
brought close under the optical combination.
Page 230
Baker’s Nelson Condenser, shown in
Fig. 140, is intended for use with their
medium instruments. It has, however,
many pieces of apparatus essential to
those of a higher class. It is applicable,
indeed, to all instruments having
sufficient depth beneath the stage to
receive it. It comprises an achromatic
combination of 90° aperture, available
with all powers up to 1⁄8-inch tinted
Fig. 140.—Baker’s Nelson Achromatic glass for neutralising the yellow rays
Condenser. of artificial light, focussing adjustment,
dark-ground illuminator, large
diaphragm with rotating tube to carry oblique light stops, small wheel of
apertures, polarising prism with two selenite films, clear aperture, and
oblique light-shutter for low powers.
Baker’s Students’ Condenser (Fig. 141) is designed to take the place of
Abbe’s, and costs much less. It transmits a larger aplanatic cone of light,
and can be used either with high or low powers by removing the front lens.
It is equally useful for photo-micrographic work.
Mr. J. Mayall’s semi-cylinder or prism for oblique illumination (Fig. 142) is
a convenient form, as it permits of the semi-cylinder being tilted and placed
excentrically; in this manner, without immersion contact, and by suitable
adjustment, a dry object can be viewed with any colour of monochromatic
light. If placed in immersion contact with the slide, the utmost obliquity of
incident light can be obtained. Objects in fluid may be placed on the plane-
surface of the semi-cylinder, and illuminated by ordinary transmitted light,
or rendered “self-luminous” in a dark field, as with the hemispherical
illuminator or Wenham’s immersion paraboloid. A concave mirror with a
double arm is quite sufficient to direct the illuminating pencil. This semi-
cylinder was originally made by Tolles, of Boston, for measuring apertures,
but, at Mr. Mayall’s suggestion, Messrs. Ross mounted it as an illuminator.
Fig. 140, is intended for use with their
medium instruments. It has, however,
many pieces of apparatus essential to
those of a higher class. It is applicable,
indeed, to all instruments having
sufficient depth beneath the stage to
receive it. It comprises an achromatic
combination of 90° aperture, available
with all powers up to 1⁄8-inch tinted
Fig. 140.—Baker’s Nelson Achromatic glass for neutralising the yellow rays
Condenser. of artificial light, focussing adjustment,
dark-ground illuminator, large
diaphragm with rotating tube to carry oblique light stops, small wheel of
apertures, polarising prism with two selenite films, clear aperture, and
oblique light-shutter for low powers.
Baker’s Students’ Condenser (Fig. 141) is designed to take the place of
Abbe’s, and costs much less. It transmits a larger aplanatic cone of light,
and can be used either with high or low powers by removing the front lens.
It is equally useful for photo-micrographic work.
Mr. J. Mayall’s semi-cylinder or prism for oblique illumination (Fig. 142) is
a convenient form, as it permits of the semi-cylinder being tilted and placed
excentrically; in this manner, without immersion contact, and by suitable
adjustment, a dry object can be viewed with any colour of monochromatic
light. If placed in immersion contact with the slide, the utmost obliquity of
incident light can be obtained. Objects in fluid may be placed on the plane-
surface of the semi-cylinder, and illuminated by ordinary transmitted light,
or rendered “self-luminous” in a dark field, as with the hemispherical
illuminator or Wenham’s immersion paraboloid. A concave mirror with a
double arm is quite sufficient to direct the illuminating pencil. This semi-
cylinder was originally made by Tolles, of Boston, for measuring apertures,
but, at Mr. Mayall’s suggestion, Messrs. Ross mounted it as an illuminator.
Page 231
Fig. 141.—Optical Arrangement of Baker’s Abbe Condenser.
The spiral slot should be fixed close beneath the larger lens of the
condenser, and when properly arranged will be found a convenient mode of
obtaining oblique light.
Fig. 142.—Mayall’s Semi-Cylinder Illuminator and Spiral Diaphragms.
The Webster-Collins Universal Condenser (Fig. 143) is so well known that
it scarcely calls for any lengthy description. It is an inexpensive form of
The spiral slot should be fixed close beneath the larger lens of the
condenser, and when properly arranged will be found a convenient mode of
obtaining oblique light.
Fig. 142.—Mayall’s Semi-Cylinder Illuminator and Spiral Diaphragms.
The Webster-Collins Universal Condenser (Fig. 143) is so well known that
it scarcely calls for any lengthy description. It is an inexpensive form of
Page 232
condenser, designed in the first instance for use with the students’
microscope. It is fitted into the sub-stage; has an iris diaphragm as well as a
series of revolving diaphragms moved by a milled head screw arrangement.
Fig. 143.—The Webster-Collins Universal Condenser.
Oblique Illumination.
Wenham’s Parabolic Condenser.—Mr. Wenham’s many useful additions to
the microscope and its accessories demand especial notice. When mention
is made of the various immersion condensers (illuminators, as he preferred
to call them), his original right-angled prism, his truncated hemispherical
lens, his immersion paraboloid, and his reflex illuminator, in which rays
beyond the angle of total reflexion are utilised by reflex action from cover-
glass on to the surface of the object, every one of these well-devised
inventions will always be spoken of in terms of praise. All in their turn
conferred a great service upon the microscope, and enabled the student to
clear up difficulties that stood in the way of developing structure when
achromatic lenses and dry-objectives were considered perfect. The superior
illumination of the object was wholly due to, and effected by, reflected rays
from the object to the aperture of the objective, and obviously, reflex action
could only take place with dry-objectives. This reflex action must be
regarded as Mr. Wenham’s special discovery. It must be observed, however,
that it is not the same as the more modern achromatic appliances used for
throwing direct rays upon the object, and which proved the existence of
microscope. It is fitted into the sub-stage; has an iris diaphragm as well as a
series of revolving diaphragms moved by a milled head screw arrangement.
Fig. 143.—The Webster-Collins Universal Condenser.
Oblique Illumination.
Wenham’s Parabolic Condenser.—Mr. Wenham’s many useful additions to
the microscope and its accessories demand especial notice. When mention
is made of the various immersion condensers (illuminators, as he preferred
to call them), his original right-angled prism, his truncated hemispherical
lens, his immersion paraboloid, and his reflex illuminator, in which rays
beyond the angle of total reflexion are utilised by reflex action from cover-
glass on to the surface of the object, every one of these well-devised
inventions will always be spoken of in terms of praise. All in their turn
conferred a great service upon the microscope, and enabled the student to
clear up difficulties that stood in the way of developing structure when
achromatic lenses and dry-objectives were considered perfect. The superior
illumination of the object was wholly due to, and effected by, reflected rays
from the object to the aperture of the objective, and obviously, reflex action
could only take place with dry-objectives. This reflex action must be
regarded as Mr. Wenham’s special discovery. It must be observed, however,
that it is not the same as the more modern achromatic appliances used for
throwing direct rays upon the object, and which proved the existence of
Page 233
apertures capable of direct transmission up to 27° measured in the body of
the front lens.
The most practical of Mr. Wenham’s
inventions is probably the hemispherical
lens, since adopted by Messrs. Ross in
connection with their excellent Zentmayer
stand, and which has proved eminently
serviceable. But the fact is that devices of
the kind for obtaining direct oblique light
require a thin stage, and therefore most of
those who possess the earlier-made
microscope stand would doubtless hail the
appearance of any appliance which will
convert axial light into oblique light; as by
so doing the possessors of such
instruments, in which the stage is generally
of considerable thickness, would enjoy the
pleasure of seeing the best resolution it is
possible to get with their dry-objectives.27
Fig. 144.—Wenham’s Parabolic Reflector.
Wenham’s Parabolic Reflector.—This will
be better understood by reference to Fig. 145, which represents it in section
A B C, and shows that the rays of light r r′ r′′, entering perpendicularly at
its surface C, and then reflected by its parabolic surface A B to a focus at F,
can form no part of the largest pencil of light admitted by the object-glass
and represented by G F H; but an object placed at F will interrupt the rays
and be strongly illuminated. A stop at S prevents any light from passing
through direct from the mirror.
In the microscope the parabolic reflector fits into the cylindrical fitting
under the stage, and the adjustment of its focus upon the object is made by
giving it a spiral motion when fitted in—that is, carefully pushing it up or
down at the same time that it is turned round by the milled edge B B. It
must then be focussed by the rack and pinion motion. As the rays of light
must be parallel when they enter it, a flat mirror, which in this case should
be added to the instrument, is generally used; daylight will then require only
the front lens.
The most practical of Mr. Wenham’s
inventions is probably the hemispherical
lens, since adopted by Messrs. Ross in
connection with their excellent Zentmayer
stand, and which has proved eminently
serviceable. But the fact is that devices of
the kind for obtaining direct oblique light
require a thin stage, and therefore most of
those who possess the earlier-made
microscope stand would doubtless hail the
appearance of any appliance which will
convert axial light into oblique light; as by
so doing the possessors of such
instruments, in which the stage is generally
of considerable thickness, would enjoy the
pleasure of seeing the best resolution it is
possible to get with their dry-objectives.27
Fig. 144.—Wenham’s Parabolic Reflector.
Wenham’s Parabolic Reflector.—This will
be better understood by reference to Fig. 145, which represents it in section
A B C, and shows that the rays of light r r′ r′′, entering perpendicularly at
its surface C, and then reflected by its parabolic surface A B to a focus at F,
can form no part of the largest pencil of light admitted by the object-glass
and represented by G F H; but an object placed at F will interrupt the rays
and be strongly illuminated. A stop at S prevents any light from passing
through direct from the mirror.
In the microscope the parabolic reflector fits into the cylindrical fitting
under the stage, and the adjustment of its focus upon the object is made by
giving it a spiral motion when fitted in—that is, carefully pushing it up or
down at the same time that it is turned round by the milled edge B B. It
must then be focussed by the rack and pinion motion. As the rays of light
must be parallel when they enter it, a flat mirror, which in this case should
be added to the instrument, is generally used; daylight will then require only
Page 234
direct reflection, but the rays from an artificial source will have to be made
parallel by placing a side condenser between the light and the mirror, about
1¾ inch from the former and 4½ inches from the latter. Nearly the whole
surface of the mirror should be equally illuminated; this may be tested by
temporarily placing upon it a card or piece of white paper. Parallel rays can
also be obtained from the concave mirror, if the light is placed about 2½
inches from it. Dark-ground illumination is not suitable for very transparent
objects—that is, unless there is a considerable difference in their index of
refraction, or they are pervaded by air-cells.
Fig. 145.—Parabolic Reflector.
One very remarkable example of this may be seen in the tracheal system of
insects. If any of the transparent larvæ of the various kinds of gnat be
mounted in gelatine and glycerine jelly, slightly warmed but not enough to
parallel by placing a side condenser between the light and the mirror, about
1¾ inch from the former and 4½ inches from the latter. Nearly the whole
surface of the mirror should be equally illuminated; this may be tested by
temporarily placing upon it a card or piece of white paper. Parallel rays can
also be obtained from the concave mirror, if the light is placed about 2½
inches from it. Dark-ground illumination is not suitable for very transparent
objects—that is, unless there is a considerable difference in their index of
refraction, or they are pervaded by air-cells.
Fig. 145.—Parabolic Reflector.
One very remarkable example of this may be seen in the tracheal system of
insects. If any of the transparent larvæ of the various kinds of gnat be
mounted in gelatine and glycerine jelly, slightly warmed but not enough to
Page 235
kill the insect outright, about the third day the fluids circulating in the body
will be absorbed and replaced by air. Illuminated by the parabolic
condenser, and viewed with a binocular microscope, and a low power, the
gnat-larva becomes a superb object. The body of the insect is but faintly
visible, and in its place is displayed a marvellous tracheal skeleton, with the
tubes standing out in perspective, shining brilliantly, like a structure of
burnished silver. Unfortunately, such objects are not permanent, for when
the whole of the water dries up, the tracheal tubes either collapse or become
refilled with fluid.
As to the blackness of field, and luminosity of the object, this depends upon
excess of light from the paraboloid received beyond the angle of aperture of
the object-glass. It is found in practice that more and more of the inner
annulus of rays from the paraboloid has to be stopped off, until at last, with
high-angled objectives, it is scarcely possible to obtain a black field.
The light, on the whole, most suitable for this method of illumination is
lamp, the rays of which should in all cases be rendered more parallel by
means of a large plano-convex lens, or condenser.
Wenham’s Immersion Condenser.—Mr.
Wenham, in the year 1856, described
various forms of oblique illuminators, one
of which was an immersion; a simple Fig. 146.—Wenham’s Hemispherical Lens.
right-angled prism, connected by a fluid
medium of oil of cloves. This, however, was abandoned for a nearly
hemispherical lens connected with the slide, and although an improvement,
did not touch the point of excellence Mr. Wenham was looking for.
Ultimately he adopted a semi-circular disc of glass of the exact form and
size represented in the drawing, Fig. 146, having a quarter-inch radius, with
a well-polished rounded edge, the sides being grasped by a simple kind of
open clip attached to the sub-stage, the fluid medium used for connecting
the upper surface with the slide being either water, glycerine, or oil; an
increase of oblique illumination being obtained by swinging the ordinary
mirror sideways. By means of an illuminator of the kind difficult objects
mounted in balsam are resolved. This simple piece of glass collects and
concentrates light in a marvellous manner, and is by no means a bad
will be absorbed and replaced by air. Illuminated by the parabolic
condenser, and viewed with a binocular microscope, and a low power, the
gnat-larva becomes a superb object. The body of the insect is but faintly
visible, and in its place is displayed a marvellous tracheal skeleton, with the
tubes standing out in perspective, shining brilliantly, like a structure of
burnished silver. Unfortunately, such objects are not permanent, for when
the whole of the water dries up, the tracheal tubes either collapse or become
refilled with fluid.
As to the blackness of field, and luminosity of the object, this depends upon
excess of light from the paraboloid received beyond the angle of aperture of
the object-glass. It is found in practice that more and more of the inner
annulus of rays from the paraboloid has to be stopped off, until at last, with
high-angled objectives, it is scarcely possible to obtain a black field.
The light, on the whole, most suitable for this method of illumination is
lamp, the rays of which should in all cases be rendered more parallel by
means of a large plano-convex lens, or condenser.
Wenham’s Immersion Condenser.—Mr.
Wenham, in the year 1856, described
various forms of oblique illuminators, one
of which was an immersion; a simple Fig. 146.—Wenham’s Hemispherical Lens.
right-angled prism, connected by a fluid
medium of oil of cloves. This, however, was abandoned for a nearly
hemispherical lens connected with the slide, and although an improvement,
did not touch the point of excellence Mr. Wenham was looking for.
Ultimately he adopted a semi-circular disc of glass of the exact form and
size represented in the drawing, Fig. 146, having a quarter-inch radius, with
a well-polished rounded edge, the sides being grasped by a simple kind of
open clip attached to the sub-stage, the fluid medium used for connecting
the upper surface with the slide being either water, glycerine, or oil; an
increase of oblique illumination being obtained by swinging the ordinary
mirror sideways. By means of an illuminator of the kind difficult objects
mounted in balsam are resolved. This simple piece of glass collects and
concentrates light in a marvellous manner, and is by no means a bad
Page 236
substitute for some of the more costly forms of achromatic condenser. It can
be used either in fluid contact with the slide, or dry, as an ordinary
condenser.
Mr. Wenham subsequently contrived a small truncated glass paraboloid, for
use in fluid contact with the slide; water, glycerine, oil, or other substance
being employed as a contact medium. The rays of light in this illuminator,
being internally reflected from a convex surface of glass, impinge obliquely
on the under surface of the slide, and are transmitted by the fluid uniting
medium, and internally reflected from the upper surface of the cover-glass
to the objective. To use the reflex illuminator efficiently it must be racked
up to a level with the stage. The centre of rotation is then set true by a dot
on the fitting, seen with a low power, a drop of water is then placed on the
top, and upon this the slide is laid. Minute objects on the slide must be
found either by the aid of a low power, by their greater brilliancy, or by
rotating the illuminator; the effect on the podura scale is superb, the whole
scale appearing dotted with bright blue spots in a zig-zag direction. Objects
for this illuminator should be especially selected and mounted.
The Amici Prism, originally designed for
oblique illumination, consists of a flattened
triangular glass prism, the two narrower
sides of which are slightly convex, while
the third or broadest side forms the
reflecting surface. When properly used, it is
capable of transmitting a very oblique
pencil of light. The prism is either
mounted, as in Fig. 147, for slipping into
Fig. 147.—The Amici Prism. the fitting of the sub-stage, or on an
independent stand, as arranged for Powell’s
microscope, page 85, Fig. 56.
Method of Employing the Achromatic Condenser to the Greatest
Advantage.
be used either in fluid contact with the slide, or dry, as an ordinary
condenser.
Mr. Wenham subsequently contrived a small truncated glass paraboloid, for
use in fluid contact with the slide; water, glycerine, oil, or other substance
being employed as a contact medium. The rays of light in this illuminator,
being internally reflected from a convex surface of glass, impinge obliquely
on the under surface of the slide, and are transmitted by the fluid uniting
medium, and internally reflected from the upper surface of the cover-glass
to the objective. To use the reflex illuminator efficiently it must be racked
up to a level with the stage. The centre of rotation is then set true by a dot
on the fitting, seen with a low power, a drop of water is then placed on the
top, and upon this the slide is laid. Minute objects on the slide must be
found either by the aid of a low power, by their greater brilliancy, or by
rotating the illuminator; the effect on the podura scale is superb, the whole
scale appearing dotted with bright blue spots in a zig-zag direction. Objects
for this illuminator should be especially selected and mounted.
The Amici Prism, originally designed for
oblique illumination, consists of a flattened
triangular glass prism, the two narrower
sides of which are slightly convex, while
the third or broadest side forms the
reflecting surface. When properly used, it is
capable of transmitting a very oblique
pencil of light. The prism is either
mounted, as in Fig. 147, for slipping into
Fig. 147.—The Amici Prism. the fitting of the sub-stage, or on an
independent stand, as arranged for Powell’s
microscope, page 85, Fig. 56.
Method of Employing the Achromatic Condenser to the Greatest
Advantage.
Page 237
Its Illumination.—Good daylight is the best for general work. The
microscope should be placed near a window with a northern aspect. Direct
sunlight should never be utilised; the best light is that reflected from a white
cloud. A good paraffin lamp is the most serviceable artificial source of light,
and it is quite under control. As an illuminant more often brought into
requisition in the smoky atmosphere of towns, the paraffin lamp is on the
whole the handiest and the most useful. If gas-light can be brought into use
as suggested for micro-photography, with the incandescent mantle, it will
be found to be the purest and best form of artificial illumination for the
microscope. Among paraffin lamps those constructed by Baker and Swift
are all that can be desired.28
Sectional view of the
Optical Arrangement of the
Aplanatic Bull’s-eye Lens,
fitted in gymbal on the front
of the lamp. Fig. 148.—Baker’s Microscope Lamp.
As the chimneys of these lamps are made of metal, and blackened, no
reflected light disturbs the eye. Care must be taken to have the wick evenly
microscope should be placed near a window with a northern aspect. Direct
sunlight should never be utilised; the best light is that reflected from a white
cloud. A good paraffin lamp is the most serviceable artificial source of light,
and it is quite under control. As an illuminant more often brought into
requisition in the smoky atmosphere of towns, the paraffin lamp is on the
whole the handiest and the most useful. If gas-light can be brought into use
as suggested for micro-photography, with the incandescent mantle, it will
be found to be the purest and best form of artificial illumination for the
microscope. Among paraffin lamps those constructed by Baker and Swift
are all that can be desired.28
Sectional view of the
Optical Arrangement of the
Aplanatic Bull’s-eye Lens,
fitted in gymbal on the front
of the lamp. Fig. 148.—Baker’s Microscope Lamp.
As the chimneys of these lamps are made of metal, and blackened, no
reflected light disturbs the eye. Care must be taken to have the wick evenly
Page 238
trimmed; the metal chimney has a glazed front, giving exit to the rays of
light, the flat of the flame being used with low powers, and the image of the
flame being reflected by a plane mirror to give equal illumination of the
whole field. In working with high powers, the lamp is turned with the flame
edge-wise, and at the same time the mirror must be dispensed with. By
working, as it is termed, directly on the edge of the flame, the illumination
is greatly increased, and a band of light can be concentrated on any part of
the preparation it is desired to make a careful study of.
To obtain the best results, time and care must be given to the illumination of
the object. The lamp and microscope having been placed in position, a low
power is first used and the smallest diaphragm. On looking through the
microscope it will probably be observed that the image of the diaphragm is
not in the centre of the field; by moving the centring screw of the condenser
this may be adjusted. The low power is then replaced by a high power, the
largest diaphragm used, and the bacteria or diatom brought into focus. The
diaphragm must now be replaced by one of medium size, and by racking
the condenser up and down, a point will be arrived at when the image of the
edge of the flame appears as an intensely bright band of light. If this is not
exactly in the centre of the field the centring screw of the condenser must
again be adjusted. With regard to the use of diaphragms, various sizes
should be tried while focussing with the fine adjustment, at the same time
using the correction colour; in this way we obtain the sharpest possible
image. When the condenser has been accurately centred, it will still be
necessary to focus it for each individual specimen, so as to correct for
difference in the thickness of slides and the layers of mounting medium.
Correction for different thickness of cover-glasses must be made by the aid
of the collar adjustment in the following way: a high-power eye-piece is
substituted for the ordinary eye-piece, and the faults in the image will
thereby be intensified. By moving the collar completely round, first in one
direction and then in the other, while carefully observing the effect of the
image, it will be seen to become obviously worse whichever way the collar
is turned. The collar must then be turned through gradually diminishing
distances until an intermediate point is reached at which the best image
results with the high-power eye-piece, and on replacing this by the low-
power eye-piece the sharpest possible image will be obtained.
light, the flat of the flame being used with low powers, and the image of the
flame being reflected by a plane mirror to give equal illumination of the
whole field. In working with high powers, the lamp is turned with the flame
edge-wise, and at the same time the mirror must be dispensed with. By
working, as it is termed, directly on the edge of the flame, the illumination
is greatly increased, and a band of light can be concentrated on any part of
the preparation it is desired to make a careful study of.
To obtain the best results, time and care must be given to the illumination of
the object. The lamp and microscope having been placed in position, a low
power is first used and the smallest diaphragm. On looking through the
microscope it will probably be observed that the image of the diaphragm is
not in the centre of the field; by moving the centring screw of the condenser
this may be adjusted. The low power is then replaced by a high power, the
largest diaphragm used, and the bacteria or diatom brought into focus. The
diaphragm must now be replaced by one of medium size, and by racking
the condenser up and down, a point will be arrived at when the image of the
edge of the flame appears as an intensely bright band of light. If this is not
exactly in the centre of the field the centring screw of the condenser must
again be adjusted. With regard to the use of diaphragms, various sizes
should be tried while focussing with the fine adjustment, at the same time
using the correction colour; in this way we obtain the sharpest possible
image. When the condenser has been accurately centred, it will still be
necessary to focus it for each individual specimen, so as to correct for
difference in the thickness of slides and the layers of mounting medium.
Correction for different thickness of cover-glasses must be made by the aid
of the collar adjustment in the following way: a high-power eye-piece is
substituted for the ordinary eye-piece, and the faults in the image will
thereby be intensified. By moving the collar completely round, first in one
direction and then in the other, while carefully observing the effect of the
image, it will be seen to become obviously worse whichever way the collar
is turned. The collar must then be turned through gradually diminishing
distances until an intermediate point is reached at which the best image
results with the high-power eye-piece, and on replacing this by the low-
power eye-piece the sharpest possible image will be obtained.
Page 239
Effect of the Sub-stage Condenser.—The sub-stage condenser gives the
most powerful illumination when it has been racked up until it almost
touches the specimen. It produces a cone of rays of very short focus, and
the apex of the cone should correspond with the particular bacterium or
group of bacterias under observation. The effect of the condenser without a
diaphragm is to obliterate what Koch has termed a structure picture. If the
component parts of a tissue section were colourless and of the same
refractive power as the medium in which the section is mounted, nothing
would be visible under the microscope. As, however, the cells and their
nuclei and the tissues do not differ in this respect, the rays which pass
through them are diffracted, and an image of lines and shadows is
developed. If in such a tissue there were minute coloured objects, and if it
were possible to mount the tissue in a medium of exactly the same
refractive power, the tissue being then invisible, the detection of the
coloured objects would be much facilitated. This is exactly what is required
in dealing with bacteria which has been stained with aniline dyes, and the
desired result can be obtained by the use of the sub-stage condenser.
If we use the full aperture of the condenser the greatly converged rays play
on the component parts of the tissue, light enters from all sides, the shadows
disappear, and the structure picture is lost. If now a diaphragm is inserted,
so that we are practically only dealing with parallel rays, the structure
picture reappears. As the diaphragm is gradually increased in size the
structure picture gradually becomes less and less distinct, while the colour
picture, the image of the stained bacteria, becomes more and more intense.
When, therefore, bacteria in the living condition and unstained tissues are
examined, a diaphragm must be used, and when the attention is to be
concentrated upon the stained bacteria in a section or in a cover-glass
preparation the diaphragm must be removed and the field flooded with light
—(Crookshank).
The wide-angle condenser, it will be understood, consists of a combination
of lenses, which concentrate all the light entering them to a small point, and
the condenser must be so accurately focussed that this brilliant cone of
light, when it emerges from the upper lens of the condenser, falls upon the
object from all directions, forming a wide-angle cone of light, at the apex of
most powerful illumination when it has been racked up until it almost
touches the specimen. It produces a cone of rays of very short focus, and
the apex of the cone should correspond with the particular bacterium or
group of bacterias under observation. The effect of the condenser without a
diaphragm is to obliterate what Koch has termed a structure picture. If the
component parts of a tissue section were colourless and of the same
refractive power as the medium in which the section is mounted, nothing
would be visible under the microscope. As, however, the cells and their
nuclei and the tissues do not differ in this respect, the rays which pass
through them are diffracted, and an image of lines and shadows is
developed. If in such a tissue there were minute coloured objects, and if it
were possible to mount the tissue in a medium of exactly the same
refractive power, the tissue being then invisible, the detection of the
coloured objects would be much facilitated. This is exactly what is required
in dealing with bacteria which has been stained with aniline dyes, and the
desired result can be obtained by the use of the sub-stage condenser.
If we use the full aperture of the condenser the greatly converged rays play
on the component parts of the tissue, light enters from all sides, the shadows
disappear, and the structure picture is lost. If now a diaphragm is inserted,
so that we are practically only dealing with parallel rays, the structure
picture reappears. As the diaphragm is gradually increased in size the
structure picture gradually becomes less and less distinct, while the colour
picture, the image of the stained bacteria, becomes more and more intense.
When, therefore, bacteria in the living condition and unstained tissues are
examined, a diaphragm must be used, and when the attention is to be
concentrated upon the stained bacteria in a section or in a cover-glass
preparation the diaphragm must be removed and the field flooded with light
—(Crookshank).
The wide-angle condenser, it will be understood, consists of a combination
of lenses, which concentrate all the light entering them to a small point, and
the condenser must be so accurately focussed that this brilliant cone of
light, when it emerges from the upper lens of the condenser, falls upon the
object from all directions, forming a wide-angle cone of light, at the apex of
Page 240
which the object must be placed (see Fig. 149). That is to say, the object is
illuminated by a cone of rays passing through it in all directions.
There are, however, objects which
require a fully illuminated field,
when the lamp should be turned
round and the Herschel lens
condenser (shown in section, Fig.
148) should be used to collect the
Fig. 149.—Front Lens of Condenser. light and throw it upon the mirror.
For moderate powers, as a four-tenth
or one-fifth, the condenser should be used a little below the focus to give an
even illumination over the whole field. Moreover, as to the use of the
condenser for defining general objects, it must be borne in mind that to
show different kinds of structure different apertures in the iris diaphragm
are necessary, and that whereas some objects show their structure better
with a large angle of light cut down in intensity by the use of blue glass,
others show better with a small pencil of direct rays. For the resolution of
diatoms it is often necessary to use oblique light only, and for this purpose
diaphragms with central patches are used, the iris diaphragm being opened
to its full extent. An annular ring of oblique light emerges from the
condenser upon the object, and it is in this manner also that dark-ground
illumination is obtained with moderate and low powers.
THE DIAPHRAGM.
Fig. 150.—The Diaphragm.
The early form of diaphragm in use was that shown in Fig. 150.
illuminated by a cone of rays passing through it in all directions.
There are, however, objects which
require a fully illuminated field,
when the lamp should be turned
round and the Herschel lens
condenser (shown in section, Fig.
148) should be used to collect the
Fig. 149.—Front Lens of Condenser. light and throw it upon the mirror.
For moderate powers, as a four-tenth
or one-fifth, the condenser should be used a little below the focus to give an
even illumination over the whole field. Moreover, as to the use of the
condenser for defining general objects, it must be borne in mind that to
show different kinds of structure different apertures in the iris diaphragm
are necessary, and that whereas some objects show their structure better
with a large angle of light cut down in intensity by the use of blue glass,
others show better with a small pencil of direct rays. For the resolution of
diatoms it is often necessary to use oblique light only, and for this purpose
diaphragms with central patches are used, the iris diaphragm being opened
to its full extent. An annular ring of oblique light emerges from the
condenser upon the object, and it is in this manner also that dark-ground
illumination is obtained with moderate and low powers.
THE DIAPHRAGM.
Fig. 150.—The Diaphragm.
The early form of diaphragm in use was that shown in Fig. 150.
Page 241
It consists simply of a circular brass plate
with a series of circular openings of
different sizes, arranged to revolve upon
another plate by a central pin or axis, the
last being also provided with an opening as
large as the largest in the diaphragm-plate,
and corresponding in situation to the axis
of the microscope body. The holes in the
diaphragm-plate are centred and retained in
place by a bent spring in the second plate,
which rubs against the edge of the
diaphragm-plate and catches in a notch. Fig. 151.—Shutter Diaphragm.
The blank space shuts off the light from the
mirror when condensed light is about to be used. It is usually made to fit in
under the stage of the microscope. This has been almost superseded by the
iris diaphragm, originally designed by Wales, of America. It was made by
this optician for his working students’ microscope. An early form of the iris
diaphragm is seen in Fig. 151. By pressing upon the lever handle at the side
the aperture gradually closes up, and without for a moment losing sight of
the object under examination.
The Mirror.
The mode in which an object is illuminated is, in the words of the late
Andrew Ross, “second only in importance to the excellence of the glass
through which it is seen.” To ensure good illumination the mirror should be
in direct co-ordination with the objective and eye-piece; it must be regarded
as a part of the same system, and tending by a combined series of acts to a
perfect result. Illumination of the object is recognised as of three kinds or
qualities—reflected, transmitted, and refracted light. For the illumination of
transparent objects, transmitted light is brought into use; for opaque objects,
reflected light is needed.
The mirror should be about 2½ or 3 inches in diameter, and it must not be
fixed, but made to slide up and down the stem under the stage, so that the
rays of light emanating from it may be brought to a focus. The utility of the
with a series of circular openings of
different sizes, arranged to revolve upon
another plate by a central pin or axis, the
last being also provided with an opening as
large as the largest in the diaphragm-plate,
and corresponding in situation to the axis
of the microscope body. The holes in the
diaphragm-plate are centred and retained in
place by a bent spring in the second plate,
which rubs against the edge of the
diaphragm-plate and catches in a notch. Fig. 151.—Shutter Diaphragm.
The blank space shuts off the light from the
mirror when condensed light is about to be used. It is usually made to fit in
under the stage of the microscope. This has been almost superseded by the
iris diaphragm, originally designed by Wales, of America. It was made by
this optician for his working students’ microscope. An early form of the iris
diaphragm is seen in Fig. 151. By pressing upon the lever handle at the side
the aperture gradually closes up, and without for a moment losing sight of
the object under examination.
The Mirror.
The mode in which an object is illuminated is, in the words of the late
Andrew Ross, “second only in importance to the excellence of the glass
through which it is seen.” To ensure good illumination the mirror should be
in direct co-ordination with the objective and eye-piece; it must be regarded
as a part of the same system, and tending by a combined series of acts to a
perfect result. Illumination of the object is recognised as of three kinds or
qualities—reflected, transmitted, and refracted light. For the illumination of
transparent objects, transmitted light is brought into use; for opaque objects,
reflected light is needed.
The mirror should be about 2½ or 3 inches in diameter, and it must not be
fixed, but made to slide up and down the stem under the stage, so that the
rays of light emanating from it may be brought to a focus. The utility of the
Page 242
mirror is so obvious that it is occasionally passed over in silence by writers.
To myself it appears to be an important accessory of the microscope, and I
shall therefore proceed to combine theory with practice in what I have to
say with regard to the mirror.
Fig. 152.—Principal Focus of Mirror.
The microscope mirror should be the segment of a true sphere, and its
centre that of a true curvature. If the mirror has a true circular boundary, the
central point on line A (Fig. 152) of the reflecting surface, is the pole of the
same. The line A C is known as its principal axis, and any other straight line
through C, which meets the mirror, is its secondary axis. When the incident
axis is perfectly parallel to the principal axis, the reflected rays converge to
a point F, its principal focus. So much for the theory of the mirror. Now we
come to its practical use.
Simple as the mirror of the microscope may appear to be, if the curve of the
surface is not perfect, it will yield a secondary reflection or double pencil of
rays. The plane mirror will occasionally be found to emit more than one
reflection of the lamp-flame; this we find may be corrected by rotating the
mirror in its cell. Many years ago I proposed to meet a difficulty of the kind
by arranging a rectangular prism on a separate stand, shown in Fig. 153,
consisting of a prism A B, mounted in gimbal C, D, and E, secured to a
brass tube G, fitted to the stem, and thus made to take the place of the
mirror.
To myself it appears to be an important accessory of the microscope, and I
shall therefore proceed to combine theory with practice in what I have to
say with regard to the mirror.
Fig. 152.—Principal Focus of Mirror.
The microscope mirror should be the segment of a true sphere, and its
centre that of a true curvature. If the mirror has a true circular boundary, the
central point on line A (Fig. 152) of the reflecting surface, is the pole of the
same. The line A C is known as its principal axis, and any other straight line
through C, which meets the mirror, is its secondary axis. When the incident
axis is perfectly parallel to the principal axis, the reflected rays converge to
a point F, its principal focus. So much for the theory of the mirror. Now we
come to its practical use.
Simple as the mirror of the microscope may appear to be, if the curve of the
surface is not perfect, it will yield a secondary reflection or double pencil of
rays. The plane mirror will occasionally be found to emit more than one
reflection of the lamp-flame; this we find may be corrected by rotating the
mirror in its cell. Many years ago I proposed to meet a difficulty of the kind
by arranging a rectangular prism on a separate stand, shown in Fig. 153,
consisting of a prism A B, mounted in gimbal C, D, and E, secured to a
brass tube G, fitted to the stem, and thus made to take the place of the
mirror.
Page 243
The direct method of employing the mirror, that more generally resorted to,
is by reflecting rays from the concave surface; the plane surface is preferred
when the condenser is used. Whichever is employed, it should not be
forgotten that the optic axis must be preserved throughout, and so brought
to the centre of the open tube of the microscope. Another method is to
interpose a bull’s-eye lens, and in this way supply the mirror with a beam of
parallel rays of light. The plane side of the bull’s-eye lens should be turned
towards the lamp, so that lamp, bull’s-eye, sub-stage condenser, and
objective, are brought into an exact line, the bull’s-eye being set at right-
angles to the line. A piece of thin white paper held across the bottom of the
sub-stage will serve to show whether the rays of light are fairly parallel. The
next care is to focus the object on the stage, and then the sub-stage
condenser on the slide; further correction should be made by means of the
centring screws of the sub-stage, or by moving the bull’s-eye lens or lamp
slightly, thus perfecting the arrangements for working with parallel rays of
light.
Fig. 153.—Rectangular Prism.
Accessories of the Microscope.
is by reflecting rays from the concave surface; the plane surface is preferred
when the condenser is used. Whichever is employed, it should not be
forgotten that the optic axis must be preserved throughout, and so brought
to the centre of the open tube of the microscope. Another method is to
interpose a bull’s-eye lens, and in this way supply the mirror with a beam of
parallel rays of light. The plane side of the bull’s-eye lens should be turned
towards the lamp, so that lamp, bull’s-eye, sub-stage condenser, and
objective, are brought into an exact line, the bull’s-eye being set at right-
angles to the line. A piece of thin white paper held across the bottom of the
sub-stage will serve to show whether the rays of light are fairly parallel. The
next care is to focus the object on the stage, and then the sub-stage
condenser on the slide; further correction should be made by means of the
centring screws of the sub-stage, or by moving the bull’s-eye lens or lamp
slightly, thus perfecting the arrangements for working with parallel rays of
light.
Fig. 153.—Rectangular Prism.
Accessories of the Microscope.
Page 244
The accessories and appliances of the microscope have become so very
numerous, that any attempt to describe them and explain the uses to which
they are put would demand more space than I find myself in a position to
bestow upon them. I must therefore confine my remarks to those
accessories in more general use.
Having described the method of employing
transmitted light, I have a few words to add
with regard to the illumination of opaque
objects by reflected light. A very early and
efficient form of opaque illumination is the
well-known Lieberkühn. This has not been
entirely surpassed by more recent
inventions. The concave speculum termed a
Lieberkühn, so named after its celebrated
inventor, directly reflects down upon the
object the light received either from the
mirror or bull’s-eye lens. It consists of a
silver cap, which slides over the objective
(Fig. 154), a indicating the lower part of
the compound body, and b the objective
Fig. 154.—The Lieberkühn. over which slides the Lieberkühn, c; the
rays of light are collected to a focus upon
the object at d. The object may either be mounted on a slip of glass, or held
by the stage-forceps, f; if very small, or transparent, it may be gummed to
the dark well, e, or mounted on a Beck’s opaque disc-revolver.
Fig. 155.—Stage Forceps, for holding objects while under examination.
This holder will be found useful for the examination of opaque or other
objects that cannot be conveniently held by the stage forceps, the specimen
numerous, that any attempt to describe them and explain the uses to which
they are put would demand more space than I find myself in a position to
bestow upon them. I must therefore confine my remarks to those
accessories in more general use.
Having described the method of employing
transmitted light, I have a few words to add
with regard to the illumination of opaque
objects by reflected light. A very early and
efficient form of opaque illumination is the
well-known Lieberkühn. This has not been
entirely surpassed by more recent
inventions. The concave speculum termed a
Lieberkühn, so named after its celebrated
inventor, directly reflects down upon the
object the light received either from the
mirror or bull’s-eye lens. It consists of a
silver cap, which slides over the objective
(Fig. 154), a indicating the lower part of
the compound body, and b the objective
Fig. 154.—The Lieberkühn. over which slides the Lieberkühn, c; the
rays of light are collected to a focus upon
the object at d. The object may either be mounted on a slip of glass, or held
by the stage-forceps, f; if very small, or transparent, it may be gummed to
the dark well, e, or mounted on a Beck’s opaque disc-revolver.
Fig. 155.—Stage Forceps, for holding objects while under examination.
This holder will be found useful for the examination of opaque or other
objects that cannot be conveniently held by the stage forceps, the specimen
Page 245
being temporarily attached to it by
gum or gold size. The holder is
intended to rotate, so that every
portion of the object can be brought
into view. In this way it will be found
Fig. 156.—Beck’s Disc-holder. useful in the study of insects,
foraminifera, &c.
With the Lieberkühn, however, the illumination of opaque objects must be
more or less one-sided, and therefore, the silver side-reflector has
superseded it for general use (Fig. 157). To ensure a more perfect
illumination of the object, the bull’s-eye lens should also be used. Mr. Sorby
devised a reflector to fit over the objective. It consists of a semi-circular
cap; is, in short, a modification of the parabolic reflector. The light from the
mirror can, by slightly varying its inclination, be brought into use with this
reflector.
The silver side-reflector is usually made with a ball-and-socket joint, so that
it can be turned in any direction. It is secured to the stage of the microscope
by the pin, which drops into a hole purposely drilled to receive it, and
facility given for turning up and down, or in any position. If daylight is used
the microscope should be placed in such a position that the light from a
white cloud falls upon the speculum, but the light of the lamp is far more
manageable for use with the reflector.
Fig. 157.—Silver Side-reflector.
gum or gold size. The holder is
intended to rotate, so that every
portion of the object can be brought
into view. In this way it will be found
Fig. 156.—Beck’s Disc-holder. useful in the study of insects,
foraminifera, &c.
With the Lieberkühn, however, the illumination of opaque objects must be
more or less one-sided, and therefore, the silver side-reflector has
superseded it for general use (Fig. 157). To ensure a more perfect
illumination of the object, the bull’s-eye lens should also be used. Mr. Sorby
devised a reflector to fit over the objective. It consists of a semi-circular
cap; is, in short, a modification of the parabolic reflector. The light from the
mirror can, by slightly varying its inclination, be brought into use with this
reflector.
The silver side-reflector is usually made with a ball-and-socket joint, so that
it can be turned in any direction. It is secured to the stage of the microscope
by the pin, which drops into a hole purposely drilled to receive it, and
facility given for turning up and down, or in any position. If daylight is used
the microscope should be placed in such a position that the light from a
white cloud falls upon the speculum, but the light of the lamp is far more
manageable for use with the reflector.
Fig. 157.—Silver Side-reflector.
Page 246
The Lieberkühn is only intended to be used with low powers—a 2-inch, ½-
inch and a 2⁄3-inch. Such objects as the elytra of the diamond and other
beetles are well suited for examination.
While experimenting with a
parabolic reflector (Fig. 158), Mr.
Sorby saw the value of examining
objects under every kind of
illumination. As on viewing
specimens of iron and steel with this Fig. 158.—Sorby’s Modification of the Parabolic
reflector he found that, from the Reflector.
great obliquity of the illumination
obtained, the more brilliantly polished parts of the specimen reflected the
light beyond the aperture of the objective, and these could not be
distinguished from those parts which absorbed light, he thereupon
proceeded to place a small flat mirror in front of the objective, and cover
half its aperture, and at the same time stop off by means of a semi-
cylindrical tube the light from the parabolic reflector. This arrangement
produced the reverse appearance of that first employed, and it proved to be
a useful aid in determining structure.
The Bull’s-eye Condensing Lens.
This accessory is brought into constant use for the purpose of converging
rays from a lamp or mirror; or, for reducing the diverging rays of the lamp
to parallelism with the parabolic illuminator, or silver side-reflector. The
form in use is a plano-convex lens of about three or four inches in focal
length (Fig. 159). It is usually mounted on a brass stand, so that it may be
placed and turned in any direction, and at any height. When used by
daylight, its plane side should be turned towards the object, and the same
position maintained when used for converging the rays of light from the
lamp; but when used with the side-reflector the plane side must be towards
the lamp. Much attention has been paid to this very necessary accessory, the
bull’s-eye lens. A doublet has been brought into use which has increased the
value of the bull’s-eye condenser in bacteriological research, and in micro-
photography generally.
inch and a 2⁄3-inch. Such objects as the elytra of the diamond and other
beetles are well suited for examination.
While experimenting with a
parabolic reflector (Fig. 158), Mr.
Sorby saw the value of examining
objects under every kind of
illumination. As on viewing
specimens of iron and steel with this Fig. 158.—Sorby’s Modification of the Parabolic
reflector he found that, from the Reflector.
great obliquity of the illumination
obtained, the more brilliantly polished parts of the specimen reflected the
light beyond the aperture of the objective, and these could not be
distinguished from those parts which absorbed light, he thereupon
proceeded to place a small flat mirror in front of the objective, and cover
half its aperture, and at the same time stop off by means of a semi-
cylindrical tube the light from the parabolic reflector. This arrangement
produced the reverse appearance of that first employed, and it proved to be
a useful aid in determining structure.
The Bull’s-eye Condensing Lens.
This accessory is brought into constant use for the purpose of converging
rays from a lamp or mirror; or, for reducing the diverging rays of the lamp
to parallelism with the parabolic illuminator, or silver side-reflector. The
form in use is a plano-convex lens of about three or four inches in focal
length (Fig. 159). It is usually mounted on a brass stand, so that it may be
placed and turned in any direction, and at any height. When used by
daylight, its plane side should be turned towards the object, and the same
position maintained when used for converging the rays of light from the
lamp; but when used with the side-reflector the plane side must be towards
the lamp. Much attention has been paid to this very necessary accessory, the
bull’s-eye lens. A doublet has been brought into use which has increased the
value of the bull’s-eye condenser in bacteriological research, and in micro-
photography generally.
Page 247
Fig. 159.—Bull’s-eye Lens.
“During a recent investigation of the spherical aberration in doublets, it was
believed to be impossible to construct a doublet of the form known as
‘Herschel’s doublet’ free from aberration, although these doublets figure in
many books on optics. In a condenser made by Baker the aberration is
reduced to a minimum, 27 per cent. less than Sir John Herschel’s. This
doublet, it appears, differs from Herschel’s both in the ratio of the radii of
the meniscus, and also in the ratio of the foci of the two lenses; indeed, the
only point of similarity is in the first lens, which is crossed. To test this,
project the image of the flat lamp-flame on a piece of white card with a
plano-convex lens (the field-lens of the Huyghenian eye-piece), use first the
convex side and then the plane side towards the card, the lamp being placed
about 6 feet from the lens. Focus the lamp-flame as sharply as possible, and
“During a recent investigation of the spherical aberration in doublets, it was
believed to be impossible to construct a doublet of the form known as
‘Herschel’s doublet’ free from aberration, although these doublets figure in
many books on optics. In a condenser made by Baker the aberration is
reduced to a minimum, 27 per cent. less than Sir John Herschel’s. This
doublet, it appears, differs from Herschel’s both in the ratio of the radii of
the meniscus, and also in the ratio of the foci of the two lenses; indeed, the
only point of similarity is in the first lens, which is crossed. To test this,
project the image of the flat lamp-flame on a piece of white card with a
plano-convex lens (the field-lens of the Huyghenian eye-piece), use first the
convex side and then the plane side towards the card, the lamp being placed
about 6 feet from the lens. Focus the lamp-flame as sharply as possible, and
Page 248
a circular halo of misty light will be seen to surround the lamp-flame; but
when the plane side of the lens is made to face the card this halo of misty
light will be seen to be greatly reduced, and the brightness of the image of
the flame proportionately increased. If the lens, then, were strictly aplanatic
there should be no misty halo, all the light being concentrated in the image
of the lamp-flame, and the image of maximum brightness. In short, the
diameter of the halo or misty light is the measure of the spherical
aberration. If the condenser referred to above, having the form of minimum
aberration for two planes, be compared in the same manner with an
ordinary single bull’s-eye of the same focus, the diameter of the misty halo
will be found reduced to a radius of about 1⁄5-inch, but, with this new
condenser there is a further reduction, so that the radius of the misty halo
measures only 1⁄20-inch. These experiments are instructive, because the
brightness, or the mistiness of the microscopical image is an associated
phenomenon.”29
A sectional view of the optical arrangement of Baker’s aplanatic bull’s-eye
doublet is shown, together with lamp, in Fig. 148.
The Microscope Lamp.—The introduction of paraffin into household use
has somewhat modified our views with regard to the most suitable artificial
source of illumination. Good paraffin burns with a whiter and purer flame
than colza oil, and consequently is less liable to fatigue the eyes. The first
cost of the lamp is trifling; for a moderate sum a handy form of lamp can be
had, mounted on an adjustable sliding ring stand, and with a porcelain,
metal or paper shade, to protect the eyes from scattered rays of light. All
opticians supply accepted forms of lamps.
To give the increased effect of whiteness to the light (“white cloud
illumination” as it is termed), take a piece of tissue paper, dip it into a hot
bath of spermaceti, and, when nearly cold, cut out a circular piece and
secure it over the largest opening in the diaphragm plate. This will be found
to materially moderate and soften the light.
Beck’s Complete Lamp is constructed especially for delicate microscopical
work. It has a burner giving a flat flame; this can be rotated to enable the
edge or the flat of the flame to be used; likewise a metal chimney with two
apertures, in which 3 × 1 glass slips slide; either white or coloured glasses
when the plane side of the lens is made to face the card this halo of misty
light will be seen to be greatly reduced, and the brightness of the image of
the flame proportionately increased. If the lens, then, were strictly aplanatic
there should be no misty halo, all the light being concentrated in the image
of the lamp-flame, and the image of maximum brightness. In short, the
diameter of the halo or misty light is the measure of the spherical
aberration. If the condenser referred to above, having the form of minimum
aberration for two planes, be compared in the same manner with an
ordinary single bull’s-eye of the same focus, the diameter of the misty halo
will be found reduced to a radius of about 1⁄5-inch, but, with this new
condenser there is a further reduction, so that the radius of the misty halo
measures only 1⁄20-inch. These experiments are instructive, because the
brightness, or the mistiness of the microscopical image is an associated
phenomenon.”29
A sectional view of the optical arrangement of Baker’s aplanatic bull’s-eye
doublet is shown, together with lamp, in Fig. 148.
The Microscope Lamp.—The introduction of paraffin into household use
has somewhat modified our views with regard to the most suitable artificial
source of illumination. Good paraffin burns with a whiter and purer flame
than colza oil, and consequently is less liable to fatigue the eyes. The first
cost of the lamp is trifling; for a moderate sum a handy form of lamp can be
had, mounted on an adjustable sliding ring stand, and with a porcelain,
metal or paper shade, to protect the eyes from scattered rays of light. All
opticians supply accepted forms of lamps.
To give the increased effect of whiteness to the light (“white cloud
illumination” as it is termed), take a piece of tissue paper, dip it into a hot
bath of spermaceti, and, when nearly cold, cut out a circular piece and
secure it over the largest opening in the diaphragm plate. This will be found
to materially moderate and soften the light.
Beck’s Complete Lamp is constructed especially for delicate microscopical
work. It has a burner giving a flat flame; this can be rotated to enable the
edge or the flat of the flame to be used; likewise a metal chimney with two
apertures, in which 3 × 1 glass slips slide; either white or coloured glasses
Page 249
may be used. A Herschel aplanatic
condenser is carried on a swinging
arm, which rotates around the lamp
flame as a centre, and can be
clamped in any position. The whole
lamp has a raising and lowering
motion, with a spring clamp to hold
it in any position. The lamp is so
designed that at its lowest position
the flame is only three inches from
the table. Here the microscopist is
furnished with a lamp which will
accomplish all he may require with
regard to illumination.
Fig. 160.—Beck’s Complete Lamp.
condenser is carried on a swinging
arm, which rotates around the lamp
flame as a centre, and can be
clamped in any position. The whole
lamp has a raising and lowering
motion, with a spring clamp to hold
it in any position. The lamp is so
designed that at its lowest position
the flame is only three inches from
the table. Here the microscopist is
furnished with a lamp which will
accomplish all he may require with
regard to illumination.
Fig. 160.—Beck’s Complete Lamp.
Page 250
Fig. 162.—Glass Holder for carrying
Fig. 161.—Watson’s Microscope Lamp. Coloured Glasses.
Watson’s lamp (Fig. 161) has a metal chimney, and is somewhat simpler in
structure than those already referred to. For the student, the simpler and
cheaper form will answer every purpose. A glass holder for carrying various
tinted slips of coloured glass to act as a screen or modifier of the light is
much employed, and assists in determining fine structures (Fig. 162).
Nose-pieces and Objective Changers.
A convenient appendage to the microscope is the rotating nose-piece,
invented by Mr. Charles Brooke, F.R.S., and intended to carry two or more
objectives, whereby a saving of time is effected, and the trouble of
repeatedly screwing and unscrewing is avoided. In the application of the
nose-piece attention should be given to centring. Messrs. Baker’s objective
Fig. 161.—Watson’s Microscope Lamp. Coloured Glasses.
Watson’s lamp (Fig. 161) has a metal chimney, and is somewhat simpler in
structure than those already referred to. For the student, the simpler and
cheaper form will answer every purpose. A glass holder for carrying various
tinted slips of coloured glass to act as a screen or modifier of the light is
much employed, and assists in determining fine structures (Fig. 162).
Nose-pieces and Objective Changers.
A convenient appendage to the microscope is the rotating nose-piece,
invented by Mr. Charles Brooke, F.R.S., and intended to carry two or more
objectives, whereby a saving of time is effected, and the trouble of
repeatedly screwing and unscrewing is avoided. In the application of the
nose-piece attention should be given to centring. Messrs. Baker’s objective
Page 251
changer is intended to facilitate the placing and replacing the nose-piece in
position. This adaptation consists of a milled head, acting on three jaws,
having a universal screw thread, a decided improvement on the screw. Zeiss
has adopted a tube-sliding objective changer with centring adjustments.
Messrs. Watson met the difficulty of centring by making the nose-piece a
part of the body-tube of their microscopes (Fig. 163). This, when adapted to
the shorter body of the students’ microscope, fully compensates for want of
length.
Their triple nose-piece is constructed
with much care, and when in use is
found very effective. It is
manufactured of that very light metal
aluminium, and which minimises the
Fig. 163.—Watson’s Centring Nose-piece of strain produced by the heavier brass
Microscope. nose-piece.
Finders.—The finder affords a necessary and useful means of registering
the position of any particular object, so that it may be readily found again at
any subsequent period. In the work of examination the finder will save time
when making a special research, extending over a considerable surface.
That the finder has been of use may be
surmised from the number invented and
figured in the “Journal of the Royal
Microscopical Society.” By far the most
useful form is that of graduating the plates
of the mechanical stage, dividing a certain
portion into 100 parts. Powell and Lealand
have adopted this system in their No. 1
stands, while Baker and Watson have added
a graduated scale on silver to 1⁄100th mm. as
a finder, and also a stage micrometer in
1⁄10th and 1⁄100th of a millimetre, together
Fig. 164.—Triple Nose-pieces. with a Maltwood finder for lodging the
position of any desired portion of a
specimen under examination.
position. This adaptation consists of a milled head, acting on three jaws,
having a universal screw thread, a decided improvement on the screw. Zeiss
has adopted a tube-sliding objective changer with centring adjustments.
Messrs. Watson met the difficulty of centring by making the nose-piece a
part of the body-tube of their microscopes (Fig. 163). This, when adapted to
the shorter body of the students’ microscope, fully compensates for want of
length.
Their triple nose-piece is constructed
with much care, and when in use is
found very effective. It is
manufactured of that very light metal
aluminium, and which minimises the
Fig. 163.—Watson’s Centring Nose-piece of strain produced by the heavier brass
Microscope. nose-piece.
Finders.—The finder affords a necessary and useful means of registering
the position of any particular object, so that it may be readily found again at
any subsequent period. In the work of examination the finder will save time
when making a special research, extending over a considerable surface.
That the finder has been of use may be
surmised from the number invented and
figured in the “Journal of the Royal
Microscopical Society.” By far the most
useful form is that of graduating the plates
of the mechanical stage, dividing a certain
portion into 100 parts. Powell and Lealand
have adopted this system in their No. 1
stands, while Baker and Watson have added
a graduated scale on silver to 1⁄100th mm. as
a finder, and also a stage micrometer in
1⁄10th and 1⁄100th of a millimetre, together
Fig. 164.—Triple Nose-pieces. with a Maltwood finder for lodging the
position of any desired portion of a
specimen under examination.
Page 252
The Maltwood finder (Fig. 165) can be used with any microscope, and
without a mechanical stage. This useful finder continues to occupy a
permanent place among the accessories of the microscope. It consists of a
glass slide, 3 × 1¼ inches, on which is photographed a scale occupying a
square inch; this is divided by horizontal and vertical lines into 2,500
squares, each of which contains two numbers marking its “latitude,” or
place in the vertical series, and its “longitude,” or place in the horizontal
series. The scale is in each instance an exact distance from the bottom and
left-hand end of the glass slide; and the slide, when in use, should rest upon
the ledge of the stage of the microscope, and be made to abut against a stop,
a simple pin, about an inch and a half from the centre of the stage.
Dr. Pantacsek’s finder appears to have
some advantage over Maltwood’s, but it
cannot be used with the same facility, and
therefore will not displace an old favourite.
The Amyot finder I have long had in use; it
is efficient and inexpensive—can indeed, if Fig. 165.—Maltwood’s Finder.
misplaced or lost, be replaced by the aid of
the square and compasses.
Fig. 166.—Amyot’s Object Finder.
without a mechanical stage. This useful finder continues to occupy a
permanent place among the accessories of the microscope. It consists of a
glass slide, 3 × 1¼ inches, on which is photographed a scale occupying a
square inch; this is divided by horizontal and vertical lines into 2,500
squares, each of which contains two numbers marking its “latitude,” or
place in the vertical series, and its “longitude,” or place in the horizontal
series. The scale is in each instance an exact distance from the bottom and
left-hand end of the glass slide; and the slide, when in use, should rest upon
the ledge of the stage of the microscope, and be made to abut against a stop,
a simple pin, about an inch and a half from the centre of the stage.
Dr. Pantacsek’s finder appears to have
some advantage over Maltwood’s, but it
cannot be used with the same facility, and
therefore will not displace an old favourite.
The Amyot finder I have long had in use; it
is efficient and inexpensive—can indeed, if Fig. 165.—Maltwood’s Finder.
misplaced or lost, be replaced by the aid of
the square and compasses.
Fig. 166.—Amyot’s Object Finder.
Page 253
The Okeden finder consists of two graduated scales, one vertical, attached
to the fixed stage-plate, the other horizontal, attached to an arm carried by
the intermediate plate; the first of these scales enables the worker to “set”
the vertically-sliding plate to any determinate position in relation to the
fixed plate, while the second gives the power of setting the horizontally-
sliding plate by that of the intermediate.
Micrometers.—It is of the utmost importance to have a means of measuring
with accuracy the objects, or part of objects, under observation. The most
efficient piece of apparatus for the purpose is the micrometer eye-piece, the
earlier form of which, Jackson’s, has been described under the heading Eye-
pieces (p. 144). In the case of micrometers, as in that of most other
accessories, every optician has his own adaptation and method of
employing the same.
For the measurement of bacteria, a stage micrometer should be used with a
camera lucida. The stage micrometer consists of a slip of thin glass ruled
with a scale consisting of tenths and hundredths of a millimetre. The image
is projected on to a piece of paper placed on the table, and the drawing
made, and the object to be measured can be readily compared with the
scale.
In the Ramsden micrometer eye-
piece, as previously explained, two
fine wires are stretched across the
field of an eye-piece, one of which
can be moved by a micrometer
screw. In the field there is also a
scale with teeth, and the interval
between them corresponds to that of
the threads of the screw.
The circumference of the brass head
is usually divided into one hundred
Fig. 167.—The Ramsden Micrometer Eye- parts, and a screw with one hundred
piece.
threads to the inch is used. The
bacterium to be measured is brought
into a position in which an edge appears to be in contact with the fixed
to the fixed stage-plate, the other horizontal, attached to an arm carried by
the intermediate plate; the first of these scales enables the worker to “set”
the vertically-sliding plate to any determinate position in relation to the
fixed plate, while the second gives the power of setting the horizontally-
sliding plate by that of the intermediate.
Micrometers.—It is of the utmost importance to have a means of measuring
with accuracy the objects, or part of objects, under observation. The most
efficient piece of apparatus for the purpose is the micrometer eye-piece, the
earlier form of which, Jackson’s, has been described under the heading Eye-
pieces (p. 144). In the case of micrometers, as in that of most other
accessories, every optician has his own adaptation and method of
employing the same.
For the measurement of bacteria, a stage micrometer should be used with a
camera lucida. The stage micrometer consists of a slip of thin glass ruled
with a scale consisting of tenths and hundredths of a millimetre. The image
is projected on to a piece of paper placed on the table, and the drawing
made, and the object to be measured can be readily compared with the
scale.
In the Ramsden micrometer eye-
piece, as previously explained, two
fine wires are stretched across the
field of an eye-piece, one of which
can be moved by a micrometer
screw. In the field there is also a
scale with teeth, and the interval
between them corresponds to that of
the threads of the screw.
The circumference of the brass head
is usually divided into one hundred
Fig. 167.—The Ramsden Micrometer Eye- parts, and a screw with one hundred
piece.
threads to the inch is used. The
bacterium to be measured is brought
into a position in which an edge appears to be in contact with the fixed
Page 254
wire, and the micrometer screw is turned until the travelling wire appears to
be in contact with the other edge. The scale in the field and scale on the
milled head, together, give the number of complete turns of the screw and
the value of a fraction of a turn in separating the wires.
In the micrometer eye-piece constructed by Zeiss, the eye-piece with a glass
plate with crossed lines is carried across the field by means of a micrometer
screw. Each division on the edge of a drum corresponds to ·01 mm.
Complete revolutions of the drum are counted by means of a figured scale
in the visual field.
In the micrometer used with Zeiss’s apochromatic objectives and
compensating eye-pieces the divisions are so computed, that, with a tube-
length of 160 mm., the value of one interval represents, with each objective,
just as many micra (·0001 mm.) as there are millimetres in its focal length.
A value of tables is therefore not required for these eye-pieces, since the
focus of the lenses indicates their micrometer values within 5 per cent.
be in contact with the other edge. The scale in the field and scale on the
milled head, together, give the number of complete turns of the screw and
the value of a fraction of a turn in separating the wires.
In the micrometer eye-piece constructed by Zeiss, the eye-piece with a glass
plate with crossed lines is carried across the field by means of a micrometer
screw. Each division on the edge of a drum corresponds to ·01 mm.
Complete revolutions of the drum are counted by means of a figured scale
in the visual field.
In the micrometer used with Zeiss’s apochromatic objectives and
compensating eye-pieces the divisions are so computed, that, with a tube-
length of 160 mm., the value of one interval represents, with each objective,
just as many micra (·0001 mm.) as there are millimetres in its focal length.
A value of tables is therefore not required for these eye-pieces, since the
focus of the lenses indicates their micrometer values within 5 per cent.
Page 255
Fig. 168.—The Wollaston Camera Lucida.
The Camera Lucida will prove an extremely useful adjunct to the
micrometer, and a large number of contrivances have been devised for its
employment. There are those which project the image on to the surface of a
sheet of paper provided for the drawing, and those which project the pencil
and paper into the field of the microscope. The former method is that
usually adopted. To draw an object, with either a Wollaston camera lucida
or a neutral tint reflector, such as that of Beale’s, both of which are made to
slide on and take the place of the cap of the eye-piece, as shown in Fig. 168,
with its flat side uppermost, the whole instrument must be raised until the
edge of the prism is exactly 10 inches from a piece of paper placed upon the
table; with the latter the instrument retains its vertical position, and the
image of the object is thrown on the paper placed in front of the stand. The
The Camera Lucida will prove an extremely useful adjunct to the
micrometer, and a large number of contrivances have been devised for its
employment. There are those which project the image on to the surface of a
sheet of paper provided for the drawing, and those which project the pencil
and paper into the field of the microscope. The former method is that
usually adopted. To draw an object, with either a Wollaston camera lucida
or a neutral tint reflector, such as that of Beale’s, both of which are made to
slide on and take the place of the cap of the eye-piece, as shown in Fig. 168,
with its flat side uppermost, the whole instrument must be raised until the
edge of the prism is exactly 10 inches from a piece of paper placed upon the
table; with the latter the instrument retains its vertical position, and the
image of the object is thrown on the paper placed in front of the stand. The
Page 256
light must be so regulated that no more than is really necessary is upon the
object, whilst a full light should be thrown upon the paper. Only one eye is
to be used; and if one half of the pupil be directed over the edge of the
prism, the object will appear upon the paper, and can be traced on it by a
pencil, the point of which will also be seen. Should any blueness be visible
in the field, the prism is pushed too far on, and should be drawn back till the
colour disappears.
Fig. 169.—Microscope in position for drawing.
The position in which the microscope must
be placed is shown in the accompanying
illustration (Fig. 169).
Beale’s neutral tint reflector (Fig. 170) is
much in use, and its advantages are utility,
simplicity, and inexpensiveness.
Fig. 170.—Beale’s Neutral Tint Reflector.
object, whilst a full light should be thrown upon the paper. Only one eye is
to be used; and if one half of the pupil be directed over the edge of the
prism, the object will appear upon the paper, and can be traced on it by a
pencil, the point of which will also be seen. Should any blueness be visible
in the field, the prism is pushed too far on, and should be drawn back till the
colour disappears.
Fig. 169.—Microscope in position for drawing.
The position in which the microscope must
be placed is shown in the accompanying
illustration (Fig. 169).
Beale’s neutral tint reflector (Fig. 170) is
much in use, and its advantages are utility,
simplicity, and inexpensiveness.
Fig. 170.—Beale’s Neutral Tint Reflector.
Page 257
Fig. 171.—The Abbe Model Camera Lucida.
The Abbe model of camera lucida has been brought into use because the
projected image can be better illuminated, and is consequently so much
brighter. This form is now made in aluminium by Messrs. Watson & Sons.
In place of the image being traced by projection on paper, the reverse is the
case, both the paper and pencil are projected into the field of view. The
mirror reflects the paper on to the silvered surface of a prism placed over
the eye-lens of the eye-piece of the microscope, and it is thereby conveyed
to the eye. There is a central opening in the silvering through which
microscopic vision is obtained. It is fitted in a new manner by means of a
cloth-lined adapter, fitting over the outside of the microscope tube; this
saves all trouble in centring and ensures concentricity. Where the
instrument has capped eye-pieces, the camera lucida must be adapted to the
eye-piece, the cap being removed. The apparatus can be disconnected from
the fitting adapter by means of a sliding pin, and readily replaced, or can be
lifted over out of the way, as shown in the drawing. Being made almost
entirely in aluminium it is very much lighter than other forms of apparatus,
and does not cause vibration. It can be used with the microscope at any
The Abbe model of camera lucida has been brought into use because the
projected image can be better illuminated, and is consequently so much
brighter. This form is now made in aluminium by Messrs. Watson & Sons.
In place of the image being traced by projection on paper, the reverse is the
case, both the paper and pencil are projected into the field of view. The
mirror reflects the paper on to the silvered surface of a prism placed over
the eye-lens of the eye-piece of the microscope, and it is thereby conveyed
to the eye. There is a central opening in the silvering through which
microscopic vision is obtained. It is fitted in a new manner by means of a
cloth-lined adapter, fitting over the outside of the microscope tube; this
saves all trouble in centring and ensures concentricity. Where the
instrument has capped eye-pieces, the camera lucida must be adapted to the
eye-piece, the cap being removed. The apparatus can be disconnected from
the fitting adapter by means of a sliding pin, and readily replaced, or can be
lifted over out of the way, as shown in the drawing. Being made almost
entirely in aluminium it is very much lighter than other forms of apparatus,
and does not cause vibration. It can be used with the microscope at any
Page 258
angle, the only necessity being that the paper on which the sketch is made
should be kept at the same angle as the instrument.
Micro-Photography.
Micro-photography or photo-micrography, as it is indifferently termed, has,
to a very considerable extent, superseded the use of the camera lucida for
the delineation of images seen under the microscope. I may claim to be
among the first workers with the microscope (1841) to prove beyond a
doubt that the camera could be made to render invaluable aid to the
microscopist, whereby a great saving of time might be effected, and a
drawing obtained with greater accuracy than that of the pencil of the
draughtsman.
It was about 1864-5 that Dr. Woodward’s earlier micro-photographs were
first seen in London. His skill in the manipulation of the microscope had
been long known. His first series of photographs of test diatoms created, I
remember, quite a sensation; they have probably never been surpassed.
These were taken by sun-light, magnesium, and electric-light. I was the
recipient of a series taken at a later date (1870), and which, bound in quarto
volume, are almost as perfect in definition as any of a later date taken by
oil-immersion objectives.
The objectives used by Dr. Woodward, throughout, were a 1⁄8-inch of
Wales’s (new series), and a 1⁄16-inch immersion, of Powell & Lealand’s,
especially produced for work with the camera. The magnification varied
from 800 to 3,000 diameters, a frustule of Grammatophora Marina
magnified 2,500, and a scale of podura, marked 3,000 in my collection, are
equal in definition to those taken by a high-angle 1⁄12-inch oil-immersion.
Pathological specimens taken with lower powers are equally instructive, a
section of epithelial cancer showing both nuclei and cells with distinctness.
Dr. Maddox in 1864 was also experimentally engaged in the improvement
of the processes of photography for the purpose of promoting the work of
microscopists. His labours were attended with great success. To him we are
indebted for the gelatine dry-plate process, which gave a remarkable
should be kept at the same angle as the instrument.
Micro-Photography.
Micro-photography or photo-micrography, as it is indifferently termed, has,
to a very considerable extent, superseded the use of the camera lucida for
the delineation of images seen under the microscope. I may claim to be
among the first workers with the microscope (1841) to prove beyond a
doubt that the camera could be made to render invaluable aid to the
microscopist, whereby a great saving of time might be effected, and a
drawing obtained with greater accuracy than that of the pencil of the
draughtsman.
It was about 1864-5 that Dr. Woodward’s earlier micro-photographs were
first seen in London. His skill in the manipulation of the microscope had
been long known. His first series of photographs of test diatoms created, I
remember, quite a sensation; they have probably never been surpassed.
These were taken by sun-light, magnesium, and electric-light. I was the
recipient of a series taken at a later date (1870), and which, bound in quarto
volume, are almost as perfect in definition as any of a later date taken by
oil-immersion objectives.
The objectives used by Dr. Woodward, throughout, were a 1⁄8-inch of
Wales’s (new series), and a 1⁄16-inch immersion, of Powell & Lealand’s,
especially produced for work with the camera. The magnification varied
from 800 to 3,000 diameters, a frustule of Grammatophora Marina
magnified 2,500, and a scale of podura, marked 3,000 in my collection, are
equal in definition to those taken by a high-angle 1⁄12-inch oil-immersion.
Pathological specimens taken with lower powers are equally instructive, a
section of epithelial cancer showing both nuclei and cells with distinctness.
Dr. Maddox in 1864 was also experimentally engaged in the improvement
of the processes of photography for the purpose of promoting the work of
microscopists. His labours were attended with great success. To him we are
indebted for the gelatine dry-plate process, which gave a remarkable
Page 259
impetus to photography in general. Dr. Maddox has, for a period extending
over forty years, diligently and successfully cultivated and promoted micro-
photography. Among other workers to whom we are indebted for
improvements in micro-photography I may mention Wenham, Draper,
Shadbolt, Highley, Koch, Sternberg, Pringle, Leitz, and Pfeiffer.
Dr. Koch justly claims the credit of having extended the application of
micro-photography to the delineation of bacteria. A series of instructive
micro-photographs were published by him in 1877.
The importance of the camera has become more manifest as the work of the
bacteriologist has progressed. Koch strongly advocated micro-photography
on the ground that illustrations, especially of bacteria, should be as true to
nature as possible. Dr. Edgar Crookshank holds the same opinion, and in
support of his views we have numerous illustrations of the bacteria given in
his valuable “Text-book of Bacteriology.” But he does not disguise the truth
that there are difficulties to be encountered, the first of which is owing to
the fact that the smallest and most interesting bacteria can only be made
visible in animal tissues by staining. This drawback has been very nearly
overcome by the use of eosin-collodion. With this medium, and by shutting
off portions of the spectrum by coloured glasses, Koch succeeded in
obtaining photographs of bacteria, which were stained with blue and red
aniline dyes. This method, however, introduced a disturbing element of
another kind. Owing to the longer exposure required, the results were
wanting in definition, attributable, it was thought, to vibrations of the
apparatus produced by passing traffic, or by assistants moving about over
the floor of the laboratory.
Koch nevertheless showed, at the great meeting of the International Medical
Association in London, 1881, a series of micro-photographs of bacteria and
tissue sections, which were the admiration of all who saw them. To meet a
difficulty occasioned by the aniline dyes, Koch recommended that the
preparations should be stained brown; other experimenters found that
preparations stained either yellow or yellowish-brown gave good
photographic representations; but it is by no means an easy matter to find a
good differential stain of bacteria in the tissues, as even Bismarck brown is
not entirely successful. Other bacteriologists have encountered similar
over forty years, diligently and successfully cultivated and promoted micro-
photography. Among other workers to whom we are indebted for
improvements in micro-photography I may mention Wenham, Draper,
Shadbolt, Highley, Koch, Sternberg, Pringle, Leitz, and Pfeiffer.
Dr. Koch justly claims the credit of having extended the application of
micro-photography to the delineation of bacteria. A series of instructive
micro-photographs were published by him in 1877.
The importance of the camera has become more manifest as the work of the
bacteriologist has progressed. Koch strongly advocated micro-photography
on the ground that illustrations, especially of bacteria, should be as true to
nature as possible. Dr. Edgar Crookshank holds the same opinion, and in
support of his views we have numerous illustrations of the bacteria given in
his valuable “Text-book of Bacteriology.” But he does not disguise the truth
that there are difficulties to be encountered, the first of which is owing to
the fact that the smallest and most interesting bacteria can only be made
visible in animal tissues by staining. This drawback has been very nearly
overcome by the use of eosin-collodion. With this medium, and by shutting
off portions of the spectrum by coloured glasses, Koch succeeded in
obtaining photographs of bacteria, which were stained with blue and red
aniline dyes. This method, however, introduced a disturbing element of
another kind. Owing to the longer exposure required, the results were
wanting in definition, attributable, it was thought, to vibrations of the
apparatus produced by passing traffic, or by assistants moving about over
the floor of the laboratory.
Koch nevertheless showed, at the great meeting of the International Medical
Association in London, 1881, a series of micro-photographs of bacteria and
tissue sections, which were the admiration of all who saw them. To meet a
difficulty occasioned by the aniline dyes, Koch recommended that the
preparations should be stained brown; other experimenters found that
preparations stained either yellow or yellowish-brown gave good
photographic representations; but it is by no means an easy matter to find a
good differential stain of bacteria in the tissues, as even Bismarck brown is
not entirely successful. Other bacteriologists have encountered similar
Page 260
difficulties at the outset. Hauser succeeded in showing the value of micro-
photography in the production of pictures of impression preparations and
colonies of bacteria in nutrient-gelatine. But to give the general effect, as
well as faithfully reproduce the minute details in these preparations of
bacteria by the aid of the pencil, would in most cases create insurmountable
difficulties, except in the hand of the most accomplished draughtsman.
Hauser employed Gerlach’s apparatus, and Schleusser’s dry-plates, and
obtained his illumination by means of a small incandescent lamp, which
gave a strong white light. The preparations so photographed were for the
most part stained brown, and mounted in the ordinary way in Canada
balsam.
In 1884, Van Ermengen succeeded in photographing preparations of
comma-bacilli stained with fuchsine and methyl violet. These pictures
afforded the first practical illustration of the value of iso-chromatic plates in
micro-photography, and their introduction marks a distinct era in the
progress of micro-photography. The iso-chromatic, or more properly the
ortho-chromatic, dry-plate process was introduced because in photography
blue or violet comes out almost or quite white, while other colours, yellow
and red, are represented by a sombre shade or even by black. This is due to
the want of equality of strength between the luminous and the actinic or
chemical rays of light. In other words, the violet and blue rays are more
chemically active than any other portion of the spectrum. It was found,
then, that if plates were coloured yellow with turmeric, the blue and violet
rays were intercepted, and their actinism proportionately reduced.
“In 1881, the so-called iso-chromatic plates were introduced. The emulsion
of bromide of silver and gelatine was stained with eosin, and it was claimed
that colours could be represented with their relative intensity; chlorophyll
and other stains have also been tried, and by such methods the ordinary
gelatine dry-plates can be so treated that they will reproduce various
colours, according to their relative light intensity, and thus be rendered iso-,
or what is now known as ortho-chromatic.”
Apparatus and Material.
photography in the production of pictures of impression preparations and
colonies of bacteria in nutrient-gelatine. But to give the general effect, as
well as faithfully reproduce the minute details in these preparations of
bacteria by the aid of the pencil, would in most cases create insurmountable
difficulties, except in the hand of the most accomplished draughtsman.
Hauser employed Gerlach’s apparatus, and Schleusser’s dry-plates, and
obtained his illumination by means of a small incandescent lamp, which
gave a strong white light. The preparations so photographed were for the
most part stained brown, and mounted in the ordinary way in Canada
balsam.
In 1884, Van Ermengen succeeded in photographing preparations of
comma-bacilli stained with fuchsine and methyl violet. These pictures
afforded the first practical illustration of the value of iso-chromatic plates in
micro-photography, and their introduction marks a distinct era in the
progress of micro-photography. The iso-chromatic, or more properly the
ortho-chromatic, dry-plate process was introduced because in photography
blue or violet comes out almost or quite white, while other colours, yellow
and red, are represented by a sombre shade or even by black. This is due to
the want of equality of strength between the luminous and the actinic or
chemical rays of light. In other words, the violet and blue rays are more
chemically active than any other portion of the spectrum. It was found,
then, that if plates were coloured yellow with turmeric, the blue and violet
rays were intercepted, and their actinism proportionately reduced.
“In 1881, the so-called iso-chromatic plates were introduced. The emulsion
of bromide of silver and gelatine was stained with eosin, and it was claimed
that colours could be represented with their relative intensity; chlorophyll
and other stains have also been tried, and by such methods the ordinary
gelatine dry-plates can be so treated that they will reproduce various
colours, according to their relative light intensity, and thus be rendered iso-,
or what is now known as ortho-chromatic.”
Apparatus and Material.
Page 261
Apparatus and Material used in micro-photography have, from time to
time, been greatly varied by different workers, some preferring to use the
microscope in the vertical position with the camera superimposed or fitted
on the eye-piece of the microscope tube; others, again, prefer that both the
microscope and the camera should be arrayed horizontally. In another form
the ordinary microscope is dispensed with and the objective stage and
mirror are adapted to the front of the camera, together with a suitable
arrangement for holding the object. Lastly, the camera is lain aside, and an
operating-room rendered impervious to light, takes its place, and the image
is projected and focussed upon a ground glass screen held in its place by a
separate support. This method has been made practical since the
introduction into microscopy by Zeiss of the projection eye-piece. It is well
known that micro-photographs can be produced by employing these
projection eye-pieces, as well as for screen illustrations in the lecture-room.
Fig. 172.—Swift’s Horizontal Apparatus.
With regard to the position of the microscope and camera, the horizontal
affords greater stability than the vertical, and is on this account to be
preferred. The simplest apparatus consists of a camera fixed upon a base
board, four or five feet in length, upon which the microscope can be
clamped, and which also carries the lamp and bull’s-eye lens (Fig. 172).
This arrangement I have found economical and useful. No more elaborate
arrangement is actually necessary. Sunlight is no doubt the best, but a good
paraffin lamp is a handy and available illuminant.
With the former, and rapid plates, a short exposure of three or four seconds,
even when high powers are used, is found sufficient; whereas, with the
paraffin lamp it will vary from three to ten minutes.
time, been greatly varied by different workers, some preferring to use the
microscope in the vertical position with the camera superimposed or fitted
on the eye-piece of the microscope tube; others, again, prefer that both the
microscope and the camera should be arrayed horizontally. In another form
the ordinary microscope is dispensed with and the objective stage and
mirror are adapted to the front of the camera, together with a suitable
arrangement for holding the object. Lastly, the camera is lain aside, and an
operating-room rendered impervious to light, takes its place, and the image
is projected and focussed upon a ground glass screen held in its place by a
separate support. This method has been made practical since the
introduction into microscopy by Zeiss of the projection eye-piece. It is well
known that micro-photographs can be produced by employing these
projection eye-pieces, as well as for screen illustrations in the lecture-room.
Fig. 172.—Swift’s Horizontal Apparatus.
With regard to the position of the microscope and camera, the horizontal
affords greater stability than the vertical, and is on this account to be
preferred. The simplest apparatus consists of a camera fixed upon a base
board, four or five feet in length, upon which the microscope can be
clamped, and which also carries the lamp and bull’s-eye lens (Fig. 172).
This arrangement I have found economical and useful. No more elaborate
arrangement is actually necessary. Sunlight is no doubt the best, but a good
paraffin lamp is a handy and available illuminant.
With the former, and rapid plates, a short exposure of three or four seconds,
even when high powers are used, is found sufficient; whereas, with the
paraffin lamp it will vary from three to ten minutes.
Page 262
Walmsley gives the following table for exposures with the lamp:—
1½-inch objective 3 to 45 seconds.
2⁄3-inch " 7 to 90 "
4⁄10-inch " ½ to 3 minutes.
1⁄5-inch " 2 to 7 "
1⁄10-inch " 4 to 10 "
For micro-photography the following practical rules must be observed. The
sub-stage condenser may be dispensed with when low powers are used, as
well as the mirror, and the lamp so placed that the image of the flat of the
flame appears accurately adjusted in the centre of the field of the
microscope. The bull’s-eye lens is so interposed, that the image of the flame
disappears, and the whole field becomes equally illuminated with high
powers; the sub-stage achromatic condenser must be used, and a greater
intensity of illumination is obtained by placing the lamp-flame edgeways. It
is advisable to begin the practice of micro-photography with low powers,
and a trial experiment should be made with some well-known object as the
blow-fly’s tongue.
Dr. Crookshank is of opinion that, in the case of micro-organisms when
their biological characters are studied under low powers of the microscope,
photographs are preferable, because they give a more faithful representation
of the object. A micro-organism, even under the highest powers of the
microscope, is so minute an object, that to represent it in a drawing requires
a very delicate touch, and it is only too easy to make a picture which gives
an erroneous impression to those who have not seen the original.
Photography enables the scientific worker to record rapid changes, and it is
quite possible as the art advances we may find the film more sensitive than
the human retina, and that it will bring out details in bacteria which would
be otherwise unrecognised. The result, therefore, of experience is that in
research laboratories it will come into more general use as a faithful and
graphic method. I cannot better bring these observations to a close than by
giving a quotation from Dr. Piersoll’s practical method of obtaining micro-
photographs.
1½-inch objective 3 to 45 seconds.
2⁄3-inch " 7 to 90 "
4⁄10-inch " ½ to 3 minutes.
1⁄5-inch " 2 to 7 "
1⁄10-inch " 4 to 10 "
For micro-photography the following practical rules must be observed. The
sub-stage condenser may be dispensed with when low powers are used, as
well as the mirror, and the lamp so placed that the image of the flat of the
flame appears accurately adjusted in the centre of the field of the
microscope. The bull’s-eye lens is so interposed, that the image of the flame
disappears, and the whole field becomes equally illuminated with high
powers; the sub-stage achromatic condenser must be used, and a greater
intensity of illumination is obtained by placing the lamp-flame edgeways. It
is advisable to begin the practice of micro-photography with low powers,
and a trial experiment should be made with some well-known object as the
blow-fly’s tongue.
Dr. Crookshank is of opinion that, in the case of micro-organisms when
their biological characters are studied under low powers of the microscope,
photographs are preferable, because they give a more faithful representation
of the object. A micro-organism, even under the highest powers of the
microscope, is so minute an object, that to represent it in a drawing requires
a very delicate touch, and it is only too easy to make a picture which gives
an erroneous impression to those who have not seen the original.
Photography enables the scientific worker to record rapid changes, and it is
quite possible as the art advances we may find the film more sensitive than
the human retina, and that it will bring out details in bacteria which would
be otherwise unrecognised. The result, therefore, of experience is that in
research laboratories it will come into more general use as a faithful and
graphic method. I cannot better bring these observations to a close than by
giving a quotation from Dr. Piersoll’s practical method of obtaining micro-
photographs.
Page 263
The three essential conditions to ensure success in micro-photography are:
—(1) Satisfactory apparatus; (2) good illumination; (3) suitable
preparations. With high amplifications (1,000 diameters and over), the
conditions are greatly changed by the approach to the limit both of the
shortness of the focus of the objective and of the length of the camera
which can be advantageously used; for the first experience leads to the
adoption of the 1⁄12-inch, for the second four feet is the limit, since a given
high amplification, say 2,000 diameters, can be more satisfactorily and
more conveniently obtained with a superior 1⁄12-inch connection with
suitable optical means to increase the initial magnifying power of the
objective, than with an unaided 1⁄25-inch lens, and the plate removed to a
greater distance. Until quite recently the various amplifiers offered the best
means of increasing the power of an objective, but the introduction of the
projection-oculars of Zeiss is an accessory piece of apparatus, far superior
to any older device. These projection-oculars resemble ordinary
microscopical oculars or eye-pieces only in general form and name, being
optically a projection-objective in connection with a collecting lens. The
new oil-immersion apochromatic lenses, in combination with these
projection-oculars, form undoubtedly the more efficient equipment for
high-power work; it is as true for high-power photography as for
microscopical observation in general, that the best results are obtained with
fine and necessarily expensive, optical appliances. If for the satisfactory
study of the intimate structure of a cell, or of a micro-organism, the most
improved immersion lenses are necessary, it is to be expected that, for the
successful photography of the same, tools at least as good are needed.
Sunlight certainly affords the most satisfactory illumination whereby good
micro-photographs can be obtained, as well as for recording microscopical
images. That by good lamp-light fair impressions of objects under extreme
magnification can be secured is encouraging, but the negatives produced by
such illumination seldom, if ever, possess the characteristics of a really
good sunlight negative, where the sharpest details are combined with an
exquisite softness and harmony of half-tones.
If the mirror of the microscope be of good size, it will only be necessary to
make an arm on which to support the removed mirror outside some
southerly exposed window, since it is desirable to have a greater distance
between the mirror and the stage than would be possible were the mirror
—(1) Satisfactory apparatus; (2) good illumination; (3) suitable
preparations. With high amplifications (1,000 diameters and over), the
conditions are greatly changed by the approach to the limit both of the
shortness of the focus of the objective and of the length of the camera
which can be advantageously used; for the first experience leads to the
adoption of the 1⁄12-inch, for the second four feet is the limit, since a given
high amplification, say 2,000 diameters, can be more satisfactorily and
more conveniently obtained with a superior 1⁄12-inch connection with
suitable optical means to increase the initial magnifying power of the
objective, than with an unaided 1⁄25-inch lens, and the plate removed to a
greater distance. Until quite recently the various amplifiers offered the best
means of increasing the power of an objective, but the introduction of the
projection-oculars of Zeiss is an accessory piece of apparatus, far superior
to any older device. These projection-oculars resemble ordinary
microscopical oculars or eye-pieces only in general form and name, being
optically a projection-objective in connection with a collecting lens. The
new oil-immersion apochromatic lenses, in combination with these
projection-oculars, form undoubtedly the more efficient equipment for
high-power work; it is as true for high-power photography as for
microscopical observation in general, that the best results are obtained with
fine and necessarily expensive, optical appliances. If for the satisfactory
study of the intimate structure of a cell, or of a micro-organism, the most
improved immersion lenses are necessary, it is to be expected that, for the
successful photography of the same, tools at least as good are needed.
Sunlight certainly affords the most satisfactory illumination whereby good
micro-photographs can be obtained, as well as for recording microscopical
images. That by good lamp-light fair impressions of objects under extreme
magnification can be secured is encouraging, but the negatives produced by
such illumination seldom, if ever, possess the characteristics of a really
good sunlight negative, where the sharpest details are combined with an
exquisite softness and harmony of half-tones.
If the mirror of the microscope be of good size, it will only be necessary to
make an arm on which to support the removed mirror outside some
southerly exposed window, since it is desirable to have a greater distance
between the mirror and the stage than would be possible were the mirror
Page 264
attached in its usual place. Where the microscope mirror is too small to be
satisfactorily used, a rectangular wood-framed looking-glass is readily
mounted, with the aid of a few strips of wood, so as to turn about both axes.
The rays from the plane side of the mirror should pass through a condensing
lens (of 8-10-inch focus, if possible), so placed that they are brought to a
focus before reaching the plane of the object. The exact position of the
condensing lens is a matter of experience; usually, however, the most
favourable illumination is obtained at that point where the field is brilliantly
and uniformly illuminated, just before the rays form the image source of
light; the nearer the focus the less disturbance from diffraction rings.
Ordinary objectives will require the employment of monochromatic light—
produced either by a deep blue solution of ammonia-sulphate of copper, or
by the green glass screen—since the optical and actinic foci do not usually
perfectly coincide. Powers up to the ¾-inch will require no further
condenser; with the ¼ or 1⁄6-inch objectives, the low power (1 or ¾-inch)
serves with advantage as an achromatic condenser, when attached to the
sub-stage. The Abbe condenser, although so important for fine
microscopical investigation, is not adapted to photography unless a very
wide cone of light is desired, which, for the majority of preparations, is
some advantage; a low-power objective, used as a condenser, is found to be
more satisfactory than the Abbe with a small diaphragm.30
The greatest delicacy in manipulation is necessary, as in working with a 1⁄12-
inch objective a turn too much of the fine adjustment will cause the image
to vanish. With fine preparations of bacteria it is not easy to trace the image,
and hence the advantage of commencing with a well-marked object, as that
of the fly’s tongue. The development and fixation of the image must be
proceeded with as in the ordinary photographic process. In the text-books of
photography full accounts of failures will be found, their causes and
prevention. Numerous papers and suggestions for micro-photographic work
will also be found scattered throughout the “Journal of the Royal
Microscopical Society.”
The Projection Eye-piece has become an essential part of micro-
photography, and it is so arranged that it may be employed with advantage
with objectives of either the apochromatic or ordinary series for
satisfactorily used, a rectangular wood-framed looking-glass is readily
mounted, with the aid of a few strips of wood, so as to turn about both axes.
The rays from the plane side of the mirror should pass through a condensing
lens (of 8-10-inch focus, if possible), so placed that they are brought to a
focus before reaching the plane of the object. The exact position of the
condensing lens is a matter of experience; usually, however, the most
favourable illumination is obtained at that point where the field is brilliantly
and uniformly illuminated, just before the rays form the image source of
light; the nearer the focus the less disturbance from diffraction rings.
Ordinary objectives will require the employment of monochromatic light—
produced either by a deep blue solution of ammonia-sulphate of copper, or
by the green glass screen—since the optical and actinic foci do not usually
perfectly coincide. Powers up to the ¾-inch will require no further
condenser; with the ¼ or 1⁄6-inch objectives, the low power (1 or ¾-inch)
serves with advantage as an achromatic condenser, when attached to the
sub-stage. The Abbe condenser, although so important for fine
microscopical investigation, is not adapted to photography unless a very
wide cone of light is desired, which, for the majority of preparations, is
some advantage; a low-power objective, used as a condenser, is found to be
more satisfactory than the Abbe with a small diaphragm.30
The greatest delicacy in manipulation is necessary, as in working with a 1⁄12-
inch objective a turn too much of the fine adjustment will cause the image
to vanish. With fine preparations of bacteria it is not easy to trace the image,
and hence the advantage of commencing with a well-marked object, as that
of the fly’s tongue. The development and fixation of the image must be
proceeded with as in the ordinary photographic process. In the text-books of
photography full accounts of failures will be found, their causes and
prevention. Numerous papers and suggestions for micro-photographic work
will also be found scattered throughout the “Journal of the Royal
Microscopical Society.”
The Projection Eye-piece has become an essential part of micro-
photography, and it is so arranged that it may be employed with advantage
with objectives of either the apochromatic or ordinary series for
Page 265
photographic purposes, projecting an exquisitely sharp image of the object
on the plate. A diaphragm between the lenses limits the field, and a sharp
image of it should appear on the screen when the eye-piece is adjusted. The
adjustment may be effected by revolving the eye-piece cap in a spiral slot,
so that the eye or top lens is either brought closer or removed farther away
from the diaphragm, as may be required, and divisions and a reader are
usually provided for registering positions. Such eye-pieces are made to fit
any size microscope body.
Initial magnifying powers:—
English length of tube 10-in. 3 and 6.
Continental " " 6-in. 2 and 4.
The microscope and camera (Fig.
173) are here seen to be part of the
same instrument. The bellows of the
camera have an extension varying
from 6 in. to 30 in. The board on
which the microscope and limelight
jet are fixed is made to turn out of
the line of the camera to facilitate
adjusting the instrument and radiant,
either limelight, electric light or
paraffin lamp; when this is done the
board carrying the same is turned
back to a stop which brings the
microscope into a central position
with the focussing screen. An
adjustment is supplied at the side of
the camera, geared to the slow
movement, for finely focussing the
object upon the screen. A light-
excluding connection is fitted to the
front of the camera and microscope;
immediately behind this, in the Fig. 173.—Baker’s Pringle Vertical Micro-
bellows, is an exposing shutter which photographic Apparatus.
is manipulated by means of a small
on the plate. A diaphragm between the lenses limits the field, and a sharp
image of it should appear on the screen when the eye-piece is adjusted. The
adjustment may be effected by revolving the eye-piece cap in a spiral slot,
so that the eye or top lens is either brought closer or removed farther away
from the diaphragm, as may be required, and divisions and a reader are
usually provided for registering positions. Such eye-pieces are made to fit
any size microscope body.
Initial magnifying powers:—
English length of tube 10-in. 3 and 6.
Continental " " 6-in. 2 and 4.
The microscope and camera (Fig.
173) are here seen to be part of the
same instrument. The bellows of the
camera have an extension varying
from 6 in. to 30 in. The board on
which the microscope and limelight
jet are fixed is made to turn out of
the line of the camera to facilitate
adjusting the instrument and radiant,
either limelight, electric light or
paraffin lamp; when this is done the
board carrying the same is turned
back to a stop which brings the
microscope into a central position
with the focussing screen. An
adjustment is supplied at the side of
the camera, geared to the slow
movement, for finely focussing the
object upon the screen. A light-
excluding connection is fitted to the
front of the camera and microscope;
immediately behind this, in the Fig. 173.—Baker’s Pringle Vertical Micro-
bellows, is an exposing shutter which photographic Apparatus.
is manipulated by means of a small
Page 266
milled head. Two focussing screens are usually supplied, one grey, and one
patent plate, together with a double dark slide.
Mr. Andrew Pringle’s vertical micro-photographic apparatus is an excellent
form; it consists of a heavy base and brass support, carrying a quarter-plate
camera, grey and plain glass focussing screen, double dark back, camera
extending to 24 inches, and turning aside as shown in Fig 173. It is light-
tight in all its connections.
To secure uniform results in micro-photography, only thin preparations,
which lie as nearly as possible in one plane, can be relied upon for good and
perfect negatives.
An electric arc lamp specially designed for
micro-photographic work, wherever the
electric current is available, is that known
as “the Ross-Hepworth projection arc
lamp.” The advantage gained by this form
of lamp is not only on account of the ease
with which it may be employed, but also on
account of its superior power and quality. It
is of primary importance that the lamp
employed to convert the electricity into
light should be of a good and reliable
pattern. It is not essential that it should be
automatic in its working—many
Fig. 174.—Ross’s Arc Lamp.
experienced micro-photographers
preferring a simple hand-feed lamp to the
one of a more complicated kind, being so much less difficult to keep in
order. A good hand-feed microscope-lamp has the advantage of greater
simplicity and portability.
The argand gas-light arranged for me many years ago for micro-
photography may be employed with advantage. It is clean, and always
ready for use when brought down to the table attached by a piece of india-
rubber tubing. The incandescent form of burner enhances its value, since
the light is thereby rendered whiter. The arrangement is shown in the
diagrammatic drawing, Fig. 175.
patent plate, together with a double dark slide.
Mr. Andrew Pringle’s vertical micro-photographic apparatus is an excellent
form; it consists of a heavy base and brass support, carrying a quarter-plate
camera, grey and plain glass focussing screen, double dark back, camera
extending to 24 inches, and turning aside as shown in Fig 173. It is light-
tight in all its connections.
To secure uniform results in micro-photography, only thin preparations,
which lie as nearly as possible in one plane, can be relied upon for good and
perfect negatives.
An electric arc lamp specially designed for
micro-photographic work, wherever the
electric current is available, is that known
as “the Ross-Hepworth projection arc
lamp.” The advantage gained by this form
of lamp is not only on account of the ease
with which it may be employed, but also on
account of its superior power and quality. It
is of primary importance that the lamp
employed to convert the electricity into
light should be of a good and reliable
pattern. It is not essential that it should be
automatic in its working—many
Fig. 174.—Ross’s Arc Lamp.
experienced micro-photographers
preferring a simple hand-feed lamp to the
one of a more complicated kind, being so much less difficult to keep in
order. A good hand-feed microscope-lamp has the advantage of greater
simplicity and portability.
The argand gas-light arranged for me many years ago for micro-
photography may be employed with advantage. It is clean, and always
ready for use when brought down to the table attached by a piece of india-
rubber tubing. The incandescent form of burner enhances its value, since
the light is thereby rendered whiter. The arrangement is shown in the
diagrammatic drawing, Fig. 175.
Page 267
Over the argand burner B, is a pale-blue glass chimney, resting on a wire
gauze, stage A; this secures a uniform current of air. The colour of the flame
may be still more influenced by a disc of neutral tint, or other coloured
glass, inserted into the circular opening at E, in a half-cylinder of metal, G,
used to cut off all extraneous light; can be rotated on the stage by the ivory
nob at H, a metallic reflector I, attached to the standard rod, on being
brought parallel to F serves to concentrate the light and send it on to the
bull’s-eye, and through it to the mirror, or directly to the photo-microscopic
camera.
Fig. 175.—Table Incandescent Gas-lamp.
By removing the shield G, and bringing the shade M over the burner, it is at
once converted into a useful microscopical lamp, for all ordinary purposes.
The screw R clamps the lamp-flame at any height, while the support N
gauze, stage A; this secures a uniform current of air. The colour of the flame
may be still more influenced by a disc of neutral tint, or other coloured
glass, inserted into the circular opening at E, in a half-cylinder of metal, G,
used to cut off all extraneous light; can be rotated on the stage by the ivory
nob at H, a metallic reflector I, attached to the standard rod, on being
brought parallel to F serves to concentrate the light and send it on to the
bull’s-eye, and through it to the mirror, or directly to the photo-microscopic
camera.
Fig. 175.—Table Incandescent Gas-lamp.
By removing the shield G, and bringing the shade M over the burner, it is at
once converted into a useful microscopical lamp, for all ordinary purposes.
The screw R clamps the lamp-flame at any height, while the support N
Page 268
carries a water-bath O, or a plate P, both of which will be found useful in
preparing and mounting objects.
A special incandescent gas-lamp is made by Messrs. R. & J. Beck.
Polarisation of Light.
Common light moves in two planes at right angles to each other, while
polarised light moves in one plane only. Common light may be turned into
polarised light either by transmission or reflection; in the first instance, one
of the planes of common light is got rid of by reflection; in the other, by
absorption. Huyghens was one of the first physicists to notice that a ray of
light has not the same properties in every part of its circumference, and he
compared it to a magnet or a collection of magnets; and supposed that the
minute particles of which it was said to be composed had different poles,
which, when acted on in certain ways, arranged themselves in particular
positions; and thence the term polarisation, a term having neither reference
to cause nor effect. It is to Malus, however, who, in 1808, discovered
polarisation by reflection, that we are indebted for the series of splendid
phenomena which have since that period been developed; phenomena of
such surpassing beauty as to exceed most ordinary objects presented to the
eye under the microscope.
Certainly no more misleading name could well have been found to describe
the causation, in one particular direction, of small displacements in the
medium, through which the light waves are made to pass.
The effect of “polarising” light is simply to alter the directions of the
vibrations of light, and allow of certain waves to pass which are vibrating in
one direction only, vertical, horizontal, or oblique, as the case may be. The
most efficient agent discovered for the polarisation of light is that of Iceland
spar, cut and mounted as a “Nicol” prism.
By cutting crystals of Iceland spar into two parts, at a particular angle, and
cementing them together again in the reverse way, Nicol succeeded in
showing that one of the two polarising pencils could be totally deflected to
preparing and mounting objects.
A special incandescent gas-lamp is made by Messrs. R. & J. Beck.
Polarisation of Light.
Common light moves in two planes at right angles to each other, while
polarised light moves in one plane only. Common light may be turned into
polarised light either by transmission or reflection; in the first instance, one
of the planes of common light is got rid of by reflection; in the other, by
absorption. Huyghens was one of the first physicists to notice that a ray of
light has not the same properties in every part of its circumference, and he
compared it to a magnet or a collection of magnets; and supposed that the
minute particles of which it was said to be composed had different poles,
which, when acted on in certain ways, arranged themselves in particular
positions; and thence the term polarisation, a term having neither reference
to cause nor effect. It is to Malus, however, who, in 1808, discovered
polarisation by reflection, that we are indebted for the series of splendid
phenomena which have since that period been developed; phenomena of
such surpassing beauty as to exceed most ordinary objects presented to the
eye under the microscope.
Certainly no more misleading name could well have been found to describe
the causation, in one particular direction, of small displacements in the
medium, through which the light waves are made to pass.
The effect of “polarising” light is simply to alter the directions of the
vibrations of light, and allow of certain waves to pass which are vibrating in
one direction only, vertical, horizontal, or oblique, as the case may be. The
most efficient agent discovered for the polarisation of light is that of Iceland
spar, cut and mounted as a “Nicol” prism.
By cutting crystals of Iceland spar into two parts, at a particular angle, and
cementing them together again in the reverse way, Nicol succeeded in
showing that one of the two polarising pencils could be totally deflected to
Page 269
one side, while the other is directly transmitted through the Nicol prism,
and thereby the beam of light becomes at once “polarised” in one plane
only. No apparent difference can be seen in the prism on holding it up to the
light, except it be in a very slight loss of brightness; but if another similarly
heated crystal be held before, and made to revolve around, a quarter of the
circle just where the two cross each other, total darkness results. This
phenomenon alternately recurs at every quadrature of the circle. A pair of
Nicol prisms, when appropriately mounted, constitute “a polarising
apparatus” for the microscope, one being fitted into the sub-stage, and the
other either immediately above the objective or eye-piece, where it can be
easily rotated, the object to be examined being placed on the stage of the
microscope, that is, between the polarising and analysing prisms.
Polariscope Objects.
Tuffen West, del. Edmund Evans.
and thereby the beam of light becomes at once “polarised” in one plane
only. No apparent difference can be seen in the prism on holding it up to the
light, except it be in a very slight loss of brightness; but if another similarly
heated crystal be held before, and made to revolve around, a quarter of the
circle just where the two cross each other, total darkness results. This
phenomenon alternately recurs at every quadrature of the circle. A pair of
Nicol prisms, when appropriately mounted, constitute “a polarising
apparatus” for the microscope, one being fitted into the sub-stage, and the
other either immediately above the objective or eye-piece, where it can be
easily rotated, the object to be examined being placed on the stage of the
microscope, that is, between the polarising and analysing prisms.
Polariscope Objects.
Tuffen West, del. Edmund Evans.
Page 270
Plate VIII.
The significance of polarised light centres in the fact that it affords a wider
insight into the structure of crystals, minerals, and a number of other
substances, and which could not otherwise be obtained without its aid. Its
usefulness is multifold, as even glass itself, when not properly annealed,
exhibits points of fracture, by a display of Newton’s rings. The knowledge
thus acquired is turned to account by glass manufacturers.
Double refraction.—When an incident ray of light is refracted into a crystal
of any other than the cubic system, or into compressed or unannealed glass,
it gives rise to two refracted rays which take different paths; this
phenomenon is termed double refraction. Attention was called to this in
1670, by Bartolin, who first observed it in Iceland spar; and the laws for
this substance were accurately determined by Huyghens.
Iceland spar or calc spar is a form of crystallized carbonate of lime. It is
composed of fifty-six parts of lime and forty-four parts of carbonic acid,
and is usually found in rhombohedral forms of crystallization.
To observe the phenomenon of double refraction, a rhomb of Iceland spar
may be laid on a page of a printed book, when all the letters seen through it
will appear double; the depth of the blackness of the letters is seen to be
considerably less than that of the originals, except where the two images
overlap.
In order to state the laws of the phenomena with precision, it is necessary to
attend to the crystalline form of Iceland spar, which has equal obtuse
angles. If a line be drawn through one of these corners, making equal angles
with the three edges which meet there, it, or any line parallel to it, is called
the axis of the crystal; the axis being, properly speaking, not a definite line
but a definite direction.
The angles of the crystals are the same in all specimens. If the crystal is of
such proportions that these three edges spoken of are equal, as in the
smaller crystal (Fig. 176), the axis is the direction of one of its diagonals, as
represented.
The significance of polarised light centres in the fact that it affords a wider
insight into the structure of crystals, minerals, and a number of other
substances, and which could not otherwise be obtained without its aid. Its
usefulness is multifold, as even glass itself, when not properly annealed,
exhibits points of fracture, by a display of Newton’s rings. The knowledge
thus acquired is turned to account by glass manufacturers.
Double refraction.—When an incident ray of light is refracted into a crystal
of any other than the cubic system, or into compressed or unannealed glass,
it gives rise to two refracted rays which take different paths; this
phenomenon is termed double refraction. Attention was called to this in
1670, by Bartolin, who first observed it in Iceland spar; and the laws for
this substance were accurately determined by Huyghens.
Iceland spar or calc spar is a form of crystallized carbonate of lime. It is
composed of fifty-six parts of lime and forty-four parts of carbonic acid,
and is usually found in rhombohedral forms of crystallization.
To observe the phenomenon of double refraction, a rhomb of Iceland spar
may be laid on a page of a printed book, when all the letters seen through it
will appear double; the depth of the blackness of the letters is seen to be
considerably less than that of the originals, except where the two images
overlap.
In order to state the laws of the phenomena with precision, it is necessary to
attend to the crystalline form of Iceland spar, which has equal obtuse
angles. If a line be drawn through one of these corners, making equal angles
with the three edges which meet there, it, or any line parallel to it, is called
the axis of the crystal; the axis being, properly speaking, not a definite line
but a definite direction.
The angles of the crystals are the same in all specimens. If the crystal is of
such proportions that these three edges spoken of are equal, as in the
smaller crystal (Fig. 176), the axis is the direction of one of its diagonals, as
represented.
Page 271
Any plane containing (or parallel to) the axis is called the principal plane of
the crystal.
In the next diagram, Fig. 177, the line appears double, as a b and c d, or the
dot, as e and f. Or allow a ray of light, g h, to fall thus on the crystal, it will
in its passage through be separated into two rays, h f, h e; and on coming to
the opposite surface of the crystal, will pass out at e f in the direction of i k,
parallel to g h. The plane l m n o is designated the principal section of the
crystal, and the line drawn from the solid angle l to the angle o is where the
axis of the crystal will be found; this is its optic axis. Now when a ray of
light passes along this axis, it is undivided, and there is only one image; but
in all other directions there are two images.
Fig. 176.—Axis of Crystals of Iceland Spar.
Mr. Nicol, of Edinburgh first
succeeded in making a rhomb of
Iceland spar into a single-image
prism. His method of splitting up the
crystal into two equal parts was as
follows:—
A rhomb of Iceland spar of one-
fourth of an inch in length, and about
four-eighths of an inch in breadth
the crystal.
In the next diagram, Fig. 177, the line appears double, as a b and c d, or the
dot, as e and f. Or allow a ray of light, g h, to fall thus on the crystal, it will
in its passage through be separated into two rays, h f, h e; and on coming to
the opposite surface of the crystal, will pass out at e f in the direction of i k,
parallel to g h. The plane l m n o is designated the principal section of the
crystal, and the line drawn from the solid angle l to the angle o is where the
axis of the crystal will be found; this is its optic axis. Now when a ray of
light passes along this axis, it is undivided, and there is only one image; but
in all other directions there are two images.
Fig. 176.—Axis of Crystals of Iceland Spar.
Mr. Nicol, of Edinburgh first
succeeded in making a rhomb of
Iceland spar into a single-image
prism. His method of splitting up the
crystal into two equal parts was as
follows:—
A rhomb of Iceland spar of one-
fourth of an inch in length, and about
four-eighths of an inch in breadth
Page 272
Fig. 177.—A Rhomb showing the passage of
and thickness, is divided into two
Rays of Light.
equal portions in a plane, passing
through the acute lateral angle, and
nearly touching the obtuse side angle. The sectional plane of each of these
halves must be carefully polished, and the two portions cemented firmly
together with Canada balsam, so as to form a rhomb similar to that before
division; by this management the ordinary and extraordinary rays are so
separated that only one is transmitted: the cause of this great divergence of
the rays is considered to be owing to the action of the Canada balsam, the
refractive index of which (1·549) is that between the ordinary (1·6543) and
the extraordinary (1·4833) refraction of calcareous spar, and which will
change the direction of both rays in an opposite manner before they enter
the posterior half of the combination. The direction of rays passing through
such a prism is indicated by the arrow, Fig. 178.
Polarised light cannot be distinguished
from common light, as already said, by the
naked eye; and for all experimental
purposes in polarisation, two pieces of
apparatus must be employed, one to Fig. 178.
produce polarisation, and the other to show
or an analyse it. The former is called the polariser, the latter the analyser;
and every apparatus that serves for one of these purposes will also serve for
the other.
Fig. 179.—Polariser. Fig. 179a.—Analyser.
and thickness, is divided into two
Rays of Light.
equal portions in a plane, passing
through the acute lateral angle, and
nearly touching the obtuse side angle. The sectional plane of each of these
halves must be carefully polished, and the two portions cemented firmly
together with Canada balsam, so as to form a rhomb similar to that before
division; by this management the ordinary and extraordinary rays are so
separated that only one is transmitted: the cause of this great divergence of
the rays is considered to be owing to the action of the Canada balsam, the
refractive index of which (1·549) is that between the ordinary (1·6543) and
the extraordinary (1·4833) refraction of calcareous spar, and which will
change the direction of both rays in an opposite manner before they enter
the posterior half of the combination. The direction of rays passing through
such a prism is indicated by the arrow, Fig. 178.
Polarised light cannot be distinguished
from common light, as already said, by the
naked eye; and for all experimental
purposes in polarisation, two pieces of
apparatus must be employed, one to Fig. 178.
produce polarisation, and the other to show
or an analyse it. The former is called the polariser, the latter the analyser;
and every apparatus that serves for one of these purposes will also serve for
the other.
Fig. 179.—Polariser. Fig. 179a.—Analyser.
Page 273
Polarising Apparatus for Students’ Microscope.
In all cases there are two positions, differing by 180°, which give a
minimum of light, and the two positions intermediate between these give a
maximum of light. The extent of the changes thus observed is a measure of
the completeness of the polarisation of light.
The two prisms mounted as shown in Figs. 179 and 179a constitute the
apparatus adapted to the microscope. The polariser slips into place below
the stage, and the analyser, with the prism fixed in a tube, is screwed in
above the objective.
The definition is considered by some experimenters as somewhat better if
the analyser be used above the eye-piece, and is certainly more easily
rotated.
Method of employing the Polarising Prism (Fig. 179).
—After having adapted it to slide into a groove on the
under-surface of the stage, where it is secured and kept
in place by the small milled-head screw, the other prism
Fig. 179a) is screwed on above the object-glass, and
thus passes directly into the body of the microscope.
The light from the mirror having been reflected through
them the axes of the two prisms must be made to
coincide; this is done by regulating the milled-head
screw until, by revolving the polarising prism, the field
of view is entirely darkened twice during its revolution.
If very minute salts or crystals are submitted for
examination then it will be found preferable to place the
analyser above the eye-piece, as in Fig. 180. Thus the
Fig. 180.—Prism
mounted as an Eye- polariscope is seen to consist of two parts; one for
piece. polarising, the other for analysing or testing the light.
There is no essential difference between the two parts,
except what convenience or economy may lead us to adopt; and either part,
therefore, may be used as polariser or analyser; but whichever is used as the
polariser, the other becomes the analyser.
In all cases there are two positions, differing by 180°, which give a
minimum of light, and the two positions intermediate between these give a
maximum of light. The extent of the changes thus observed is a measure of
the completeness of the polarisation of light.
The two prisms mounted as shown in Figs. 179 and 179a constitute the
apparatus adapted to the microscope. The polariser slips into place below
the stage, and the analyser, with the prism fixed in a tube, is screwed in
above the objective.
The definition is considered by some experimenters as somewhat better if
the analyser be used above the eye-piece, and is certainly more easily
rotated.
Method of employing the Polarising Prism (Fig. 179).
—After having adapted it to slide into a groove on the
under-surface of the stage, where it is secured and kept
in place by the small milled-head screw, the other prism
Fig. 179a) is screwed on above the object-glass, and
thus passes directly into the body of the microscope.
The light from the mirror having been reflected through
them the axes of the two prisms must be made to
coincide; this is done by regulating the milled-head
screw until, by revolving the polarising prism, the field
of view is entirely darkened twice during its revolution.
If very minute salts or crystals are submitted for
examination then it will be found preferable to place the
analyser above the eye-piece, as in Fig. 180. Thus the
Fig. 180.—Prism
mounted as an Eye- polariscope is seen to consist of two parts; one for
piece. polarising, the other for analysing or testing the light.
There is no essential difference between the two parts,
except what convenience or economy may lead us to adopt; and either part,
therefore, may be used as polariser or analyser; but whichever is used as the
polariser, the other becomes the analyser.
Page 274
Fig. 181.—More Modern Polariser and Analyser.
Opticians have their own methods of adapting the polariser and analyser to
their several microscopes. Watson’s special form of apparatus is represented
in Fig. 181, the polariser being adapted to the sub-stage, and the analyser to
screw into the objective.
Tourmaline.—A semi-transparent mineral, of a neutral or bluish tint, called
tourmaline, when cut into thin slices (about 1⁄20-inch thick) with their faces
parallel to their axes exhibit the same phenomena as the Nicol prism. The
only objection to which is that the transmitted polarised beam is more or
less coloured. The tourmaline to be preferred stops the most light when its
axis is at right-angles to that of the polariser, and yet admits the most when
in the same plane. Make choice of a tourmaline as perfect as possible; size
is of less importance when intended for use with the microscope.
Transmission of rays through tourmaline is only one of several ways in
which light can be polarised. When a beam of light is reflected from a
polished surface of glass, wood, ivory, leather, or any other non-metallic
substance, at an angle of 50° to 60° with the normal, it is more or less
polarised, and in like manner a reflector composed of any of these
substances may be employed as an analyser. In so using it, it should be
rotated about an axis parallel to the incident rays which are to be tested, and
the observation consists in noting whether this rotation produces changes in
the amount of reflected light.
For every reflected substance there is a particular angle of incidence, which
gives a maximum of polarisation in reflected light. It is called the polarising
Opticians have their own methods of adapting the polariser and analyser to
their several microscopes. Watson’s special form of apparatus is represented
in Fig. 181, the polariser being adapted to the sub-stage, and the analyser to
screw into the objective.
Tourmaline.—A semi-transparent mineral, of a neutral or bluish tint, called
tourmaline, when cut into thin slices (about 1⁄20-inch thick) with their faces
parallel to their axes exhibit the same phenomena as the Nicol prism. The
only objection to which is that the transmitted polarised beam is more or
less coloured. The tourmaline to be preferred stops the most light when its
axis is at right-angles to that of the polariser, and yet admits the most when
in the same plane. Make choice of a tourmaline as perfect as possible; size
is of less importance when intended for use with the microscope.
Transmission of rays through tourmaline is only one of several ways in
which light can be polarised. When a beam of light is reflected from a
polished surface of glass, wood, ivory, leather, or any other non-metallic
substance, at an angle of 50° to 60° with the normal, it is more or less
polarised, and in like manner a reflector composed of any of these
substances may be employed as an analyser. In so using it, it should be
rotated about an axis parallel to the incident rays which are to be tested, and
the observation consists in noting whether this rotation produces changes in
the amount of reflected light.
For every reflected substance there is a particular angle of incidence, which
gives a maximum of polarisation in reflected light. It is called the polarising
Page 275
angle for the substance, and its tangent is always equal to the index of
refraction of the substance; or, what amounts to the same thing, it is that
particular angle of incidence which is the complement of the angle of
refraction, so that the refracted rays are at right angles. This important law
was discovered experimentally by Sir David Brewster.
Tourmaline, like Iceland spar, is a negative uniaxial crystal; and its use as a
polariser depends on the property which it possesses of absorbing the
ordinary much more rapidly than the extraordinary ray, so that a thickness
which is tolerably transparent to the latter is almost completely opaque to
the former. Its pale cobalt blue colour enhances the beauty of certain crystal
and mineral substances, but like Iceland spar, the paler and more perfect
crystals are becoming scarce.
Selenite is another mineral of value in polarisation experiments. It is a
native crystalline hydrated sulphate of lime. A beautiful fibrous variety
called satin-gypsum is found in Derbyshire. The form of the crystal most
frequently met with is that of an oblique rectangular prism, with ten
rhomboidal faces, two of which are much larger than the rest. It is usually
split up into thin laminæ parallel to their lateral faces; each film should have
a thickness of from one-twentieth to one-sixtieth of an inch. In the two
rectangular directions these films allow perpendicular rays of polarised light
to traverse them unchanged, termed their neutral axes. In two other
directions, however, which form respectively angles of 45° with the neutral
axes, these films have the property of double refraction, a direction known
as the depolarising axis.
The thickness of the film of selenite
determines the particular tint. If,
therefore, we use a film of irregular
thickness, different colours are
presented by the different thicknesses.
These facts admit of very curious and
beautiful illustration, when used under
the object placed on the stage of the
microscope. The films employed should
Fig. 182.—Darker’s Selenite Films and Stage. be mounted between two glasses for
refraction of the substance; or, what amounts to the same thing, it is that
particular angle of incidence which is the complement of the angle of
refraction, so that the refracted rays are at right angles. This important law
was discovered experimentally by Sir David Brewster.
Tourmaline, like Iceland spar, is a negative uniaxial crystal; and its use as a
polariser depends on the property which it possesses of absorbing the
ordinary much more rapidly than the extraordinary ray, so that a thickness
which is tolerably transparent to the latter is almost completely opaque to
the former. Its pale cobalt blue colour enhances the beauty of certain crystal
and mineral substances, but like Iceland spar, the paler and more perfect
crystals are becoming scarce.
Selenite is another mineral of value in polarisation experiments. It is a
native crystalline hydrated sulphate of lime. A beautiful fibrous variety
called satin-gypsum is found in Derbyshire. The form of the crystal most
frequently met with is that of an oblique rectangular prism, with ten
rhomboidal faces, two of which are much larger than the rest. It is usually
split up into thin laminæ parallel to their lateral faces; each film should have
a thickness of from one-twentieth to one-sixtieth of an inch. In the two
rectangular directions these films allow perpendicular rays of polarised light
to traverse them unchanged, termed their neutral axes. In two other
directions, however, which form respectively angles of 45° with the neutral
axes, these films have the property of double refraction, a direction known
as the depolarising axis.
The thickness of the film of selenite
determines the particular tint. If,
therefore, we use a film of irregular
thickness, different colours are
presented by the different thicknesses.
These facts admit of very curious and
beautiful illustration, when used under
the object placed on the stage of the
microscope. The films employed should
Fig. 182.—Darker’s Selenite Films and Stage. be mounted between two glasses for
Page 276
protection. Some persons employ a large film, mounted in this way between
the plates of glass, with a raised edge, to act as a stage for supporting the
object, it is then called the “selenite stage.” The best film for the
microscope is that which gives blue, and its complementary colour yellow.
The late Mr. Darker constructed a selenite stage for the purpose (Fig. 182).
With this a mixture of colours will be brought about, by superimposing
three films, one on the other. By slight variations in their positions,
produced by means of an endless-screw motion, all the colours of the
spectrum can be shown. When objects are thus exhibited, it should be borne
in mind that all negative tints, as they are termed, are diminished, and all
positive tints increased; the effect of which is to mask the true character of
the phenomena.
For a certain thickness of selenite the ellipse will become a circle, and we
have thus what is called circularly-polarised light, which is characterised
by the property that rotation of the analyser produces no change of intensity.
Circularly-polarised light is not, however, identical with ordinary light; for
the interposition of an additional thickness of selenite converts it into
elliptically (or in a particular case into plane) polarised light.
It is necessary, for the exhibition of colour in our experiments, that the plate
of selenite should be very thin, otherwise the retardation of one component
vibration as compared with the other will be greater by several complete
periods for violet than for red, so that the ellipses will be identical for
several different colours, and the total non-suppressed light will be sensibly
white in all positions of the analyser.
Two thick plates may, however, be so combined as to produce the effect of
one thin plate. For example, two selenite plates of nearly equal thickness
may be laid one upon the other, so that the direction of greatest elasticity in
the one shall be parallel to that of least elasticity in the other. The resultant
effect in this case will be that due to the difference of their thicknesses. Two
plates so laid are said to be crossed.
the plates of glass, with a raised edge, to act as a stage for supporting the
object, it is then called the “selenite stage.” The best film for the
microscope is that which gives blue, and its complementary colour yellow.
The late Mr. Darker constructed a selenite stage for the purpose (Fig. 182).
With this a mixture of colours will be brought about, by superimposing
three films, one on the other. By slight variations in their positions,
produced by means of an endless-screw motion, all the colours of the
spectrum can be shown. When objects are thus exhibited, it should be borne
in mind that all negative tints, as they are termed, are diminished, and all
positive tints increased; the effect of which is to mask the true character of
the phenomena.
For a certain thickness of selenite the ellipse will become a circle, and we
have thus what is called circularly-polarised light, which is characterised
by the property that rotation of the analyser produces no change of intensity.
Circularly-polarised light is not, however, identical with ordinary light; for
the interposition of an additional thickness of selenite converts it into
elliptically (or in a particular case into plane) polarised light.
It is necessary, for the exhibition of colour in our experiments, that the plate
of selenite should be very thin, otherwise the retardation of one component
vibration as compared with the other will be greater by several complete
periods for violet than for red, so that the ellipses will be identical for
several different colours, and the total non-suppressed light will be sensibly
white in all positions of the analyser.
Two thick plates may, however, be so combined as to produce the effect of
one thin plate. For example, two selenite plates of nearly equal thickness
may be laid one upon the other, so that the direction of greatest elasticity in
the one shall be parallel to that of least elasticity in the other. The resultant
effect in this case will be that due to the difference of their thicknesses. Two
plates so laid are said to be crossed.
Page 277
Fig. 183.—Red is represented by perpendicular lines; Green by oblique.
The following experiments will well serve to illustrate some of the more
striking phenomena of double refraction, and will also be a useful
introduction to its practical application. Take a plate of brass (Fig. 183)
three inches by one, perforated with a series of holes from about one-
sixteenth to one-fourth of an inch in diameter; the size of the smallest
should be in accordance with the power of the objective, and the separating
power of the double refraction.
Experiment 1.—Place the brass plate so that the smallest hole shall be in the
centre of the stage of the microscope; employ a low power (1½ or 2 inches)
objective, and adjust the focus as for the ordinary microscopic object; place
the double image prism over the eye-piece, and two distinct images will be
seen; by revolving the prism, the images will describe a circle, the
circumference of which will cut the centre of the field of view; one of
which is the ordinary, the other the extraordinary ray. By moving the slide
from left to right the larger orifices will appear in the field, the images seen
will not be completely separated, but will overlap, as represented in the
figure.
Experiment 2.—Insert the Nicol’s prism into its place under the stage, still
retaining the double image prism over the eye-piece; then, by examining the
object, there will appear in some positions two images, in others only one
image; it will be seen, that at 90° this ray will be cut off, and that which was
first observed will become visible; at 180°, or one-half the circle, an
alternate change will take place; at 270°, another change; and at 360°, the
completion of the circle, the first image will reappear.
Before proceeding to make the next experiment, the position of the Nicol’s
prism should be adjusted, and its angles brought parallel with the square of
The following experiments will well serve to illustrate some of the more
striking phenomena of double refraction, and will also be a useful
introduction to its practical application. Take a plate of brass (Fig. 183)
three inches by one, perforated with a series of holes from about one-
sixteenth to one-fourth of an inch in diameter; the size of the smallest
should be in accordance with the power of the objective, and the separating
power of the double refraction.
Experiment 1.—Place the brass plate so that the smallest hole shall be in the
centre of the stage of the microscope; employ a low power (1½ or 2 inches)
objective, and adjust the focus as for the ordinary microscopic object; place
the double image prism over the eye-piece, and two distinct images will be
seen; by revolving the prism, the images will describe a circle, the
circumference of which will cut the centre of the field of view; one of
which is the ordinary, the other the extraordinary ray. By moving the slide
from left to right the larger orifices will appear in the field, the images seen
will not be completely separated, but will overlap, as represented in the
figure.
Experiment 2.—Insert the Nicol’s prism into its place under the stage, still
retaining the double image prism over the eye-piece; then, by examining the
object, there will appear in some positions two images, in others only one
image; it will be seen, that at 90° this ray will be cut off, and that which was
first observed will become visible; at 180°, or one-half the circle, an
alternate change will take place; at 270°, another change; and at 360°, the
completion of the circle, the first image will reappear.
Before proceeding to make the next experiment, the position of the Nicol’s
prism should be adjusted, and its angles brought parallel with the square of
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the stage. The true relative position of the selenite should also be
determined by noticing the natural flaws in the film, which should run
parallel with each other, and be adjusted at an angle of about 46° with the
square bars of the stage.
Experiment 3.—If we now take the plate of selenite thus prepared, and
place it under the piece of brass on the stage, we shall see, instead of the
alternate black and white images, two coloured images composed of the
constituents of white light, which will alternately change by revolving the
eye-piece at every quarter of the circle; then, by passing along the brass, the
images will overlap; and at the point at which they do so, white light will be
produced. If, by accident, the prism be placed at an angle of 45° from the
square part of the stage, no particular colour will be perceived, and it will
then illustrate the phenomena of the neutral axis of the selenite, because
when placed in the relative position no depolarisation takes place. The
phenomena of polarised light may be further illustrated by the addition of a
second double image prism, and a film of selenite adapted between the two.
The systems of coloured rings in crystals cut perpendicularly to the
principal axis of the crystal are best seen by employing the lowest object-
glass.
Biaxial Crystals.—To show perfectly the beautiful series of rings and
brushes which biaxial crystals exhibit, it becomes necessary to convert the
microscope, for the time being, into (so to speak) a wide-angled telescope.
Huyghenian Eye-piece.
Inner draw-tube.
Objective in draw-tube.
determined by noticing the natural flaws in the film, which should run
parallel with each other, and be adjusted at an angle of about 46° with the
square bars of the stage.
Experiment 3.—If we now take the plate of selenite thus prepared, and
place it under the piece of brass on the stage, we shall see, instead of the
alternate black and white images, two coloured images composed of the
constituents of white light, which will alternately change by revolving the
eye-piece at every quarter of the circle; then, by passing along the brass, the
images will overlap; and at the point at which they do so, white light will be
produced. If, by accident, the prism be placed at an angle of 45° from the
square part of the stage, no particular colour will be perceived, and it will
then illustrate the phenomena of the neutral axis of the selenite, because
when placed in the relative position no depolarisation takes place. The
phenomena of polarised light may be further illustrated by the addition of a
second double image prism, and a film of selenite adapted between the two.
The systems of coloured rings in crystals cut perpendicularly to the
principal axis of the crystal are best seen by employing the lowest object-
glass.
Biaxial Crystals.—To show perfectly the beautiful series of rings and
brushes which biaxial crystals exhibit, it becomes necessary to convert the
microscope, for the time being, into (so to speak) a wide-angled telescope.
Huyghenian Eye-piece.
Inner draw-tube.
Objective in draw-tube.
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Analysing Prism.
Objective.
Specimen under Examination.
Sub-stage Condenser.
Polarising Prism, fixed in sub-stage below.
Fig. 184.—Diagrammatic arrangement of the Polarising Microscope.
In Sub-stage: P, polarising prism; C, sub-stage condenser on stage; M,
mineral or crystal. On nose-piece: O1, objective, 4⁄10-inch; A, analysing
prism.
In Draw-tube: O2, 2 or 3 inch Objective; H, Huyghenian eye-piece.
For the purpose, screw on a low-power objective to the end of the draw-
tube (Fig. 184).31 As the light requires to be passed through the crystals at a
considerable angle, a wide-angled condenser should be employed, but it
need not be achromatic. The objective most suitable is a 4⁄10-inch, of ·64
numerical aperture, but a ¼-inch of ·71 numerical aperture, or a 1⁄3-inch of
·65 numerical aperture, will answer the purpose equally well. As the whole
of the back lens of the objective should be visible through the analysing
Nicol prism, the back lens of the objective must not be too large; thus a ½-
inch of ·65 numerical aperture will not be so effective. The analysing prism
may be placed either where it is in the drawing, below the stage, or above
the eye-piece. It works equally well above the objective, the position it
ordinarily occupies in the microscope.
For the draw-tube a 2-inch objective and a B Huyghenian eye-piece
answers very well. Before screwing the objective on to the end of the draw-
tube centre the light in the usual manner, the Nicol’s being turned so as to
give a light field, then screw the objective on to the end of the aperture, and
put the crystal on the stage, rack down the body so that the objective on the
Objective.
Specimen under Examination.
Sub-stage Condenser.
Polarising Prism, fixed in sub-stage below.
Fig. 184.—Diagrammatic arrangement of the Polarising Microscope.
In Sub-stage: P, polarising prism; C, sub-stage condenser on stage; M,
mineral or crystal. On nose-piece: O1, objective, 4⁄10-inch; A, analysing
prism.
In Draw-tube: O2, 2 or 3 inch Objective; H, Huyghenian eye-piece.
For the purpose, screw on a low-power objective to the end of the draw-
tube (Fig. 184).31 As the light requires to be passed through the crystals at a
considerable angle, a wide-angled condenser should be employed, but it
need not be achromatic. The objective most suitable is a 4⁄10-inch, of ·64
numerical aperture, but a ¼-inch of ·71 numerical aperture, or a 1⁄3-inch of
·65 numerical aperture, will answer the purpose equally well. As the whole
of the back lens of the objective should be visible through the analysing
Nicol prism, the back lens of the objective must not be too large; thus a ½-
inch of ·65 numerical aperture will not be so effective. The analysing prism
may be placed either where it is in the drawing, below the stage, or above
the eye-piece. It works equally well above the objective, the position it
ordinarily occupies in the microscope.
For the draw-tube a 2-inch objective and a B Huyghenian eye-piece
answers very well. Before screwing the objective on to the end of the draw-
tube centre the light in the usual manner, the Nicol’s being turned so as to
give a light field, then screw the objective on to the end of the aperture, and
put the crystal on the stage, rack down the body so that the objective on the
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nose-piece nearly touches the crystal, then focus with the draw-tube only.
The sub-stage condenser should be racked up close to the underside of the
crystal.
Opticians, however, have more recently furnished a special form of
microscope (The Petrological Microscope, Fig. 79, p. 112), for the use of
those students who may desire to prosecute so fascinating a study, and
determine the optic axial angles of crystals.
Fuess32 lately introduced a new form of microscope for polarising and
viewing biaxial crystals, which he believes to be needed, as in the ordinary
microscope the opening of the polariser is scarcely a third of that of the
condenser; moreover, it is not absolutely necessary that the polariser and
analyser should be Nicol’s prisms. This fact was discovered by myself
many years ago. Fuess utilises a bundle of thin glass plates, as in the older
Nuremberg polariscope. The frame holding plates can be readily adjusted at
the proper polarising angle, the analyser being the ordinary small Nicol,
screwed above the objective. The illuminator is an Abbe’s triple condenser,
of numerical aperture 1·40, which can be adjusted in the ordinary way. The
front lens of this should have a diameter of 11·12 mm. and the lower lens of
30 mm. This increase in the condenser fully compensates for the loss of
light by the bundle of glass plates, and also enables thick sections of
crystals to be examined in convergent polarised light. The ocular used
should have a large field; the A Huyghenian answers best. A suggestion to
return to the original Nuremberg polariser is very opportune, as Iceland
spar is becoming scarce.
Mr. A. Mickel accidentally discovered that an opalescent mirror can be
converted into an excellent and inexpensive substitute for the Nicol-prism
polariser.
Rotation of Plane of Polarisation.
When a plate of quartz (rock-crystal), even of considerable thickness, cut
perpendicular to the axis, is interposed between the polariser and analyser,
colour is exhibited, the tints changing as the analyser is rotated; and similar
The sub-stage condenser should be racked up close to the underside of the
crystal.
Opticians, however, have more recently furnished a special form of
microscope (The Petrological Microscope, Fig. 79, p. 112), for the use of
those students who may desire to prosecute so fascinating a study, and
determine the optic axial angles of crystals.
Fuess32 lately introduced a new form of microscope for polarising and
viewing biaxial crystals, which he believes to be needed, as in the ordinary
microscope the opening of the polariser is scarcely a third of that of the
condenser; moreover, it is not absolutely necessary that the polariser and
analyser should be Nicol’s prisms. This fact was discovered by myself
many years ago. Fuess utilises a bundle of thin glass plates, as in the older
Nuremberg polariscope. The frame holding plates can be readily adjusted at
the proper polarising angle, the analyser being the ordinary small Nicol,
screwed above the objective. The illuminator is an Abbe’s triple condenser,
of numerical aperture 1·40, which can be adjusted in the ordinary way. The
front lens of this should have a diameter of 11·12 mm. and the lower lens of
30 mm. This increase in the condenser fully compensates for the loss of
light by the bundle of glass plates, and also enables thick sections of
crystals to be examined in convergent polarised light. The ocular used
should have a large field; the A Huyghenian answers best. A suggestion to
return to the original Nuremberg polariser is very opportune, as Iceland
spar is becoming scarce.
Mr. A. Mickel accidentally discovered that an opalescent mirror can be
converted into an excellent and inexpensive substitute for the Nicol-prism
polariser.
Rotation of Plane of Polarisation.
When a plate of quartz (rock-crystal), even of considerable thickness, cut
perpendicular to the axis, is interposed between the polariser and analyser,
colour is exhibited, the tints changing as the analyser is rotated; and similar
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effects of colour are produced by employing, instead of quartz, a solution of
sugar enclosed in a tube with plain glass ends.
The action thus exerted by quartz and sugar is called rotation of the plane of
polarisation, a name which sufficiently expresses the observed phenomena.
In the case of ordinary quartz, and solutions of sugar-candy, it is necessary
to rotate the analyser in the direction of watch-hands as seen by the
observer, and the rotation of the plane of polarisation is said to be right-
handed. In the case of what is called left-handed quartz, and of solutions of
non-crystallisable sugar, the rotation of the plane of polarisation is in the
opposite direction, and the observer must rotate the analyser against watch-
hands.
Quartz belongs to the uniaxial system of crystals, and accordingly exhibits
one series of rings only, and no perfect central black cross.
On revolving the tourmaline the colour gradually changes, and passes
through all the colours of the spectrum. It can be cut to exhibit either right-
handed polarisation or left-handed polarisation and also to exhibit straight
lines.
Calc Spar.—A uniaxial crystal showing only one system of rings, and a
black cross, changing into a white cross on revolving the tourmaline.
Topaz.—A biaxial crystal exhibiting only one system of rings with one
fringe, owing to the wide separation of the axes. The fringe and colours
change on revolving the tourmaline.
Borax.—A biaxial crystal; the colours are seen to be more intense than in
topaz, but the rings not so complete—only one set of rings can be seen,
owing to their wide separation.
Rochelle Salt.—A biaxial crystal; the colours are more widely spread out
than the former, and only one set of rings seen at the same time.
Carbonate of Lead.—A biaxial crystal; axes not so far separated, and both
systems of rings are more widely spread than those of potassium nitrate.
sugar enclosed in a tube with plain glass ends.
The action thus exerted by quartz and sugar is called rotation of the plane of
polarisation, a name which sufficiently expresses the observed phenomena.
In the case of ordinary quartz, and solutions of sugar-candy, it is necessary
to rotate the analyser in the direction of watch-hands as seen by the
observer, and the rotation of the plane of polarisation is said to be right-
handed. In the case of what is called left-handed quartz, and of solutions of
non-crystallisable sugar, the rotation of the plane of polarisation is in the
opposite direction, and the observer must rotate the analyser against watch-
hands.
Quartz belongs to the uniaxial system of crystals, and accordingly exhibits
one series of rings only, and no perfect central black cross.
On revolving the tourmaline the colour gradually changes, and passes
through all the colours of the spectrum. It can be cut to exhibit either right-
handed polarisation or left-handed polarisation and also to exhibit straight
lines.
Calc Spar.—A uniaxial crystal showing only one system of rings, and a
black cross, changing into a white cross on revolving the tourmaline.
Topaz.—A biaxial crystal exhibiting only one system of rings with one
fringe, owing to the wide separation of the axes. The fringe and colours
change on revolving the tourmaline.
Borax.—A biaxial crystal; the colours are seen to be more intense than in
topaz, but the rings not so complete—only one set of rings can be seen,
owing to their wide separation.
Rochelle Salt.—A biaxial crystal; the colours are more widely spread out
than the former, and only one set of rings seen at the same time.
Carbonate of Lead.—A biaxial crystal; axes not so far separated, and both
systems of rings are more widely spread than those of potassium nitrate.
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Aragonite.—A biaxial crystal; axes widely separated, but both systems of
rings seen at the same time. A fine crystal for displaying the biaxial system.
Fig. 185.—Crystal of Potassium Nitrate.
It was long believed that all crystals had only one axis of double refraction;
but Brewster found that the greater number of crystals which occur in the
mineral kingdom have two axes of double refraction, or rather axes around
which double refraction takes place; in the axes themselves there is no
double refraction.
Potassium nitrate crystallises in six-sided prisms with angles of about 120°.
It has two axes of double refraction. These axes are each inclined about 2½°
to the axes of the prism, and 5° to each other. If, therefore, a small piece be
split off a prism of potassium nitrate with a knife driven by a sharp blow of
a hammer, and the two surfaces polished perpendicular to the axes of the
prism, so as to leave the thickness of the sixth or eighth of an inch, and then
a ray of polarised light be transmitted along the axes of the prism, the
double system of rings will be clearly visible.
When the line connecting the two axes of the crystal is inclined 45° to the
plane of primitive polarisation, a cross is seen on revolving the potassium
nitrate; it gradually assumes the form of two hyperbolic curves, as in Fig.
185. But if the tourmaline be again revolved through half a quadrant, the
black cross will be replaced by white spaces, as in the second figure. These
systems of rings have, generally speaking, the same colours as those of thin
plates, or as those of a system of rings revolving around one axis. The
orders of the colours commence at the centres of each system; but at a
certain distance, which corresponds to the sixth ring, the rings, instead of
rings seen at the same time. A fine crystal for displaying the biaxial system.
Fig. 185.—Crystal of Potassium Nitrate.
It was long believed that all crystals had only one axis of double refraction;
but Brewster found that the greater number of crystals which occur in the
mineral kingdom have two axes of double refraction, or rather axes around
which double refraction takes place; in the axes themselves there is no
double refraction.
Potassium nitrate crystallises in six-sided prisms with angles of about 120°.
It has two axes of double refraction. These axes are each inclined about 2½°
to the axes of the prism, and 5° to each other. If, therefore, a small piece be
split off a prism of potassium nitrate with a knife driven by a sharp blow of
a hammer, and the two surfaces polished perpendicular to the axes of the
prism, so as to leave the thickness of the sixth or eighth of an inch, and then
a ray of polarised light be transmitted along the axes of the prism, the
double system of rings will be clearly visible.
When the line connecting the two axes of the crystal is inclined 45° to the
plane of primitive polarisation, a cross is seen on revolving the potassium
nitrate; it gradually assumes the form of two hyperbolic curves, as in Fig.
185. But if the tourmaline be again revolved through half a quadrant, the
black cross will be replaced by white spaces, as in the second figure. These
systems of rings have, generally speaking, the same colours as those of thin
plates, or as those of a system of rings revolving around one axis. The
orders of the colours commence at the centres of each system; but at a
certain distance, which corresponds to the sixth ring, the rings, instead of
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returning and encircling each pole, encircle the two poles as an ellipse does
its two foci. If the thickness of the plate of nitre be diminished or increased,
the rings are diminished or increased according to the thickness of the
crystal.
Small specimens of various salts may be crystallised and mounted in
Canada balsam for viewing under the stage of the microscope; by arresting
crystallisation at certain stages, a greater variety of forms and colours will
be obtained: we may enumerate salicine, asparagine, acetate of copper,
phospho-borate of soda, sugar, carbonate of lime, potassium chlorate, oxalic
acid, and all the oxalates found in urine, with the other salts from the same
fluid, a few of which are shown in Plate VIII.
The late Dr. Herapath described a salt of quinine, remarkable for its
polarising properties. The crystals of this salt, when examined by reflected
light, have a brilliant emerald-green colour, with almost a metallic lustre;
they appear like portions of the elytræ of the cantharides beetle, and are also
very similar to murexide in appearance. When examined by transmitted
light, they scarcely possess any colour, there is only a slightly olive-green
tinge; but if two crystals, crossing at right-angles, be examined, the spot
where they intersect appears perfectly black, even if the crystals are not
more than one five-hundredth of an inch in thickness. If the light be in the
slightest degree polarised—as by reflection from a cloud, or by the blue
sky, or from the glass surface of the mirror of the microscope placed at the
polarising angle 65° 45′—these little prisms and films assume
complementary colours: one appears green, and the other pink, and the part
at which they cross is chocolate or deep chestnut-brown, instead of black.
Dr. Herapath succeeded in making artificial tourmalines large enough to
surmount the eye-piece of the microscope; so that all experiments with
those crystals upon polarised light may be made without the tourmaline or
Nicol’s prism. The finest rosette crystals are made as follows:—To a
moderately strong solution of Cinchonidine add a drop or two of Herapath’s
test-fluid.33 A few drops of this is placed on the centre of a glass slide, and
put aside until the first crystals are observed to be formed near the margin.
The slide should now be placed upon the stage of the microscope, and the
progress of formation of the crystals closely watched. When these are seen
to be large enough, and it is deemed necessary to stop their further
its two foci. If the thickness of the plate of nitre be diminished or increased,
the rings are diminished or increased according to the thickness of the
crystal.
Small specimens of various salts may be crystallised and mounted in
Canada balsam for viewing under the stage of the microscope; by arresting
crystallisation at certain stages, a greater variety of forms and colours will
be obtained: we may enumerate salicine, asparagine, acetate of copper,
phospho-borate of soda, sugar, carbonate of lime, potassium chlorate, oxalic
acid, and all the oxalates found in urine, with the other salts from the same
fluid, a few of which are shown in Plate VIII.
The late Dr. Herapath described a salt of quinine, remarkable for its
polarising properties. The crystals of this salt, when examined by reflected
light, have a brilliant emerald-green colour, with almost a metallic lustre;
they appear like portions of the elytræ of the cantharides beetle, and are also
very similar to murexide in appearance. When examined by transmitted
light, they scarcely possess any colour, there is only a slightly olive-green
tinge; but if two crystals, crossing at right-angles, be examined, the spot
where they intersect appears perfectly black, even if the crystals are not
more than one five-hundredth of an inch in thickness. If the light be in the
slightest degree polarised—as by reflection from a cloud, or by the blue
sky, or from the glass surface of the mirror of the microscope placed at the
polarising angle 65° 45′—these little prisms and films assume
complementary colours: one appears green, and the other pink, and the part
at which they cross is chocolate or deep chestnut-brown, instead of black.
Dr. Herapath succeeded in making artificial tourmalines large enough to
surmount the eye-piece of the microscope; so that all experiments with
those crystals upon polarised light may be made without the tourmaline or
Nicol’s prism. The finest rosette crystals are made as follows:—To a
moderately strong solution of Cinchonidine add a drop or two of Herapath’s
test-fluid.33 A few drops of this is placed on the centre of a glass slide, and
put aside until the first crystals are observed to be formed near the margin.
The slide should now be placed upon the stage of the microscope, and the
progress of formation of the crystals closely watched. When these are seen
to be large enough, and it is deemed necessary to stop their further
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development, the slide must be quickly transferred to the palm of the hand,
the warmth of which will be found sufficient to stop further crystallisation.
These crystals attract moisture, deliquesce, and should therefore be kept in a
perfectly dry place.
Fig. 186.—In this figure heraldic lines are adopted to denote colour. The dotted
parts indicate yellow, the straight lines red, the horizontal lines blue, and the
diagonal, or oblique lines, green. The arrows show the plane of the
tourmaline, a, blue stage; b, red stage of selenite employed.
To render these crystals evident, it merely remains to bring the glass-slide
upon the field of the microscope, with the selenite stage and single
tourmaline, or Nicol’s prism, beneath it; instantly the crystals assume the
two complementary colours of the stage: red and green, supposing that the
pink stage is employed; or blue and yellow, provided the blue selenite is
made use of. All those crystals at right angles to the plane of the tourmaline
produce that tint which an analysing-plate of tourmaline would produce
when at right angles to the polarising-plate; whilst those at 90° to these
educe the complementary tint, as the analysing-plate would also have done
if revolved through an arc of 90°.
the warmth of which will be found sufficient to stop further crystallisation.
These crystals attract moisture, deliquesce, and should therefore be kept in a
perfectly dry place.
Fig. 186.—In this figure heraldic lines are adopted to denote colour. The dotted
parts indicate yellow, the straight lines red, the horizontal lines blue, and the
diagonal, or oblique lines, green. The arrows show the plane of the
tourmaline, a, blue stage; b, red stage of selenite employed.
To render these crystals evident, it merely remains to bring the glass-slide
upon the field of the microscope, with the selenite stage and single
tourmaline, or Nicol’s prism, beneath it; instantly the crystals assume the
two complementary colours of the stage: red and green, supposing that the
pink stage is employed; or blue and yellow, provided the blue selenite is
made use of. All those crystals at right angles to the plane of the tourmaline
produce that tint which an analysing-plate of tourmaline would produce
when at right angles to the polarising-plate; whilst those at 90° to these
educe the complementary tint, as the analysing-plate would also have done
if revolved through an arc of 90°.
Page 285
This test is a delicate one for quinine (Fig. 186, a and b); not only do these
peculiar crystals act in the way just related, but they may be easily proved
to possess the optical properties of that remarkable salt, the sulphate of
iodo-quinine.
Fig. 187.—Polarised Crystals of Quinidine.
To test for quinidine, it is merely necessary to allow a drop of acid solution
to evaporate to dryness upon the slide, and to examine the crystalline mass
by two tourmalines, crossed at right angles, and without the stage.
Immediately little circular discs of white, with a well-defined black cross,
start into existence, should quinidine be present even in very minute traces.
These crystals are represented in Fig. 187.
If the selenite stage be employed in the examination of this object, one of
the most gorgeous appearances in the whole domain of the polarising
microscope is displayed: the black cross disappears, and is replaced by one
consisting of two colours, and divided into a cross having a red and green
fringe, whilst the four intermediate sectors are a gorgeous orange-yellow.
These appearances alter on the revolution of the analysing-plate of
tourmaline; when the blue stage is employed, the cross assumes a blue or
peculiar crystals act in the way just related, but they may be easily proved
to possess the optical properties of that remarkable salt, the sulphate of
iodo-quinine.
Fig. 187.—Polarised Crystals of Quinidine.
To test for quinidine, it is merely necessary to allow a drop of acid solution
to evaporate to dryness upon the slide, and to examine the crystalline mass
by two tourmalines, crossed at right angles, and without the stage.
Immediately little circular discs of white, with a well-defined black cross,
start into existence, should quinidine be present even in very minute traces.
These crystals are represented in Fig. 187.
If the selenite stage be employed in the examination of this object, one of
the most gorgeous appearances in the whole domain of the polarising
microscope is displayed: the black cross disappears, and is replaced by one
consisting of two colours, and divided into a cross having a red and green
fringe, whilst the four intermediate sectors are a gorgeous orange-yellow.
These appearances alter on the revolution of the analysing-plate of
tourmaline; when the blue stage is employed, the cross assumes a blue or
Page 286
yellow tint, varying according to the position of the analysing plate. These
phenomena are analogous to those exhibited by certain circular crystals of
boracic acid, and to circular discs of salicine (prepared by fusion), the
difference being that the salts of quinidine have more intense depolarising
powers than either of the other substances; the mode of preparation,
however, excludes these from consideration. Quinine prepared in the same
manner as quinidine has a very different mode of crystallisation; but it
occasionally presents circular corneous plates, also exhibiting the black
cross and white sectors, but not with one-tenth part of the brilliancy, which
of course enables us readily to discriminate the two.
Fig. 188.—Urinary Salts, seen under Polarised Light.
a, Uric acid; b, Oxalate of lime, octahedral crystals of; c, Oxalate of lime allowed
to dry, forming a black cube; d, Oxalate of lime as it occasionally appears, termed
the dumb-bell crystal.
Urinary salts are more readily seen under polarised light than by white light.
Ice doubly refracts, while water singly refracts. Ice takes the rhomboidic
form; and snow in its crystalline forms may be regarded as the skeleton
crystals of this system (Fig. 189). A sheet of clear ice, of about one inch
thick, and slowly formed in still weather, shows circular rings with a cross
by polarised light.
phenomena are analogous to those exhibited by certain circular crystals of
boracic acid, and to circular discs of salicine (prepared by fusion), the
difference being that the salts of quinidine have more intense depolarising
powers than either of the other substances; the mode of preparation,
however, excludes these from consideration. Quinine prepared in the same
manner as quinidine has a very different mode of crystallisation; but it
occasionally presents circular corneous plates, also exhibiting the black
cross and white sectors, but not with one-tenth part of the brilliancy, which
of course enables us readily to discriminate the two.
Fig. 188.—Urinary Salts, seen under Polarised Light.
a, Uric acid; b, Oxalate of lime, octahedral crystals of; c, Oxalate of lime allowed
to dry, forming a black cube; d, Oxalate of lime as it occasionally appears, termed
the dumb-bell crystal.
Urinary salts are more readily seen under polarised light than by white light.
Ice doubly refracts, while water singly refracts. Ice takes the rhomboidic
form; and snow in its crystalline forms may be regarded as the skeleton
crystals of this system (Fig. 189). A sheet of clear ice, of about one inch
thick, and slowly formed in still weather, shows circular rings with a cross
by polarised light.
Page 287
Fig. 189.—Snow Crystals.
It is probable that the conditions of
snow formation are more complex
than might be imagined, familiar as
we are with the conditions relating to
the crystallisation of water on the
earth’s surface. A great variety of
animal, vegetable, and other
substances possess a doubly refracting
Fig. 190.—Potato Starch, under Polarised Light. or depolarising structure, as: a quill
cut and laid out flat on glass; the
cornea of a sheep’s eye; skin, hair, a thin section of a finger-nail; sections of
bone, teeth, horn, silk, cotton, whalebone; stems of plants containing silica
It is probable that the conditions of
snow formation are more complex
than might be imagined, familiar as
we are with the conditions relating to
the crystallisation of water on the
earth’s surface. A great variety of
animal, vegetable, and other
substances possess a doubly refracting
Fig. 190.—Potato Starch, under Polarised Light. or depolarising structure, as: a quill
cut and laid out flat on glass; the
cornea of a sheep’s eye; skin, hair, a thin section of a finger-nail; sections of
bone, teeth, horn, silk, cotton, whalebone; stems of plants containing silica
Page 288
or flint; barley, wheat, &c. The larger-grained starches form splendid
objects; tous-les-mois, the largest, may be taken as a type of all others. This
presents a black cross, the arms of which meet at the hilum (Fig. 190). On
rotating the analyser, the black cross disappears, and at 90° is replaced by a
white cross; another, but much fainter, black cross is seen between the arms
of the white cross, no colour being perceptible. But if a thin plate of selenite
be interposed between the starch-grains and the polariser, a series of
delicate colours appear, all of which change on revolving the analyser,
becoming complementary at every quadrant of the circle. West and East
India arrow-root, sago, tapioca, and many other starch-grains, present a
similar appearance; but in proportion as the grains are smaller, so are their
markings and colourings less distinct.
Molecular Rotation.
For the purpose of studying the various interesting phenomena of molecular
rotation, a few necessary pieces of apparatus must be added to the
microscope. First, an ordinary iron three-armed retort stand, to the lower
arm of which must be attached either a polarising prism or a bundle of glass
plates inclined at the polarising angle; in the upper an analysing prism. The
fluid to be examined should be contained in a narrow glass tube about eight
inches in height, and this must be attached to the middle arm. If the prisms
be crossed before inserting a fluid possessing rotatory power, the light
passing through the analyser will be coloured. If a solution of sugar be
employed, and the light which passes through the second prism is seen to be
red, but on rotating the analyser towards the right the colour changes to
yellow, and passes through green to violet, it may be concluded that the
rotation is right-handed. If, on the contrary, the analyser requires to be
turned towards the left hand, we conclude that the polarisation is left-
handed. These phenomena are wholly distinct from those accompanying the
action of doubly refracting substances upon plane polarised light. It is not
easy to explain in a limited space the course to be followed in ascertaining
the amount of rotation produced by different substances. Monochromatic
light should be used. If we are about to examine a sugar solution with the
prisms crossed, the index attached to the analyser must first be made to
point to zero. The sugar is then introduced, when it will be necessary to
objects; tous-les-mois, the largest, may be taken as a type of all others. This
presents a black cross, the arms of which meet at the hilum (Fig. 190). On
rotating the analyser, the black cross disappears, and at 90° is replaced by a
white cross; another, but much fainter, black cross is seen between the arms
of the white cross, no colour being perceptible. But if a thin plate of selenite
be interposed between the starch-grains and the polariser, a series of
delicate colours appear, all of which change on revolving the analyser,
becoming complementary at every quadrant of the circle. West and East
India arrow-root, sago, tapioca, and many other starch-grains, present a
similar appearance; but in proportion as the grains are smaller, so are their
markings and colourings less distinct.
Molecular Rotation.
For the purpose of studying the various interesting phenomena of molecular
rotation, a few necessary pieces of apparatus must be added to the
microscope. First, an ordinary iron three-armed retort stand, to the lower
arm of which must be attached either a polarising prism or a bundle of glass
plates inclined at the polarising angle; in the upper an analysing prism. The
fluid to be examined should be contained in a narrow glass tube about eight
inches in height, and this must be attached to the middle arm. If the prisms
be crossed before inserting a fluid possessing rotatory power, the light
passing through the analyser will be coloured. If a solution of sugar be
employed, and the light which passes through the second prism is seen to be
red, but on rotating the analyser towards the right the colour changes to
yellow, and passes through green to violet, it may be concluded that the
rotation is right-handed. If, on the contrary, the analyser requires to be
turned towards the left hand, we conclude that the polarisation is left-
handed. These phenomena are wholly distinct from those accompanying the
action of doubly refracting substances upon plane polarised light. It is not
easy to explain in a limited space the course to be followed in ascertaining
the amount of rotation produced by different substances. Monochromatic
light should be used. If we are about to examine a sugar solution with the
prisms crossed, the index attached to the analyser must first be made to
point to zero. The sugar is then introduced, when it will be necessary to
Page 289
rotate the analyser 23° to the right, in order that the light may be
extinguished. This is the amount of rotation for that particular fluid at a
given density and that height of column. As the arc varies with increase or
decrease of density and height of the fluid, it is needful to reduce it to a unit
of height and density. The following formula is that given by Biot:—P =
quantity of matter in a unit of solution; d = sp. gr.; l = length of column; a =
arc of rotation; m = molecular rotation.
Then m = a/(l p d).
The application of the polarising apparatus to the microscope is of much
value in determining minute structure. It may also be defined as an
instrument of analysis; a test of difference in density between any two or
more parts of the same substance. All structures, therefore, belonging either
to the animal, vegetable, or mineral kingdom, in which the power of
unequal or double refraction is suspected to be present, are those that should
especially be re-investigated by polarised light. Some of the most delicate
of the elementary tissues of animal structure, the ultimate fibrillæ of
muscles, &c., are amongst the most interesting subjects that might be
studied with advantage under this method of investigation. The chemist
may perform the most dexterous analysis; the crystallographer may
examine crystals by the nicest determination of their forms and cleavage;
the anatomist or botanist may use the dissecting knife and microscope with
the most exquisite skill; but there are still structures in the mineral,
vegetable, and animal kingdoms which will defy all such modes of
examination, and will yield only to the magical analysis of polarised light.
Formation and Polarisation of Crystals.
The inorganic kingdom will afford to the microscopist a never-ending
number of objects of unsurpassed beauty and interest. The phenomena of
crystallisation in its varied combinations can be made a useful and
instructive occupation. Although ignorant of the means whereby the great
majority of minerals and crystals have been formed in the vast laboratory of
Nature, we can, nevertheless, imitate in a small degree Nature’s handiworks
by crystallising out a large number of substances, and watch their numerous
extinguished. This is the amount of rotation for that particular fluid at a
given density and that height of column. As the arc varies with increase or
decrease of density and height of the fluid, it is needful to reduce it to a unit
of height and density. The following formula is that given by Biot:—P =
quantity of matter in a unit of solution; d = sp. gr.; l = length of column; a =
arc of rotation; m = molecular rotation.
Then m = a/(l p d).
The application of the polarising apparatus to the microscope is of much
value in determining minute structure. It may also be defined as an
instrument of analysis; a test of difference in density between any two or
more parts of the same substance. All structures, therefore, belonging either
to the animal, vegetable, or mineral kingdom, in which the power of
unequal or double refraction is suspected to be present, are those that should
especially be re-investigated by polarised light. Some of the most delicate
of the elementary tissues of animal structure, the ultimate fibrillæ of
muscles, &c., are amongst the most interesting subjects that might be
studied with advantage under this method of investigation. The chemist
may perform the most dexterous analysis; the crystallographer may
examine crystals by the nicest determination of their forms and cleavage;
the anatomist or botanist may use the dissecting knife and microscope with
the most exquisite skill; but there are still structures in the mineral,
vegetable, and animal kingdoms which will defy all such modes of
examination, and will yield only to the magical analysis of polarised light.
Formation and Polarisation of Crystals.
The inorganic kingdom will afford to the microscopist a never-ending
number of objects of unsurpassed beauty and interest. The phenomena of
crystallisation in its varied combinations can be made a useful and
instructive occupation. Although ignorant of the means whereby the great
majority of minerals and crystals have been formed in the vast laboratory of
Nature, we can, nevertheless, imitate in a small degree Nature’s handiworks
by crystallising out a large number of substances, and watch their numerous
Page 290
transformations in the smallest appreciable quantities, when aided by the
microscope.
Among natural crystals we look for the material for the formation of our
lenses, while the varieties of granites present us with the earliest crystallised
condition of the earth’s crust as it cooled down, the structure of which is
beautifully exhibited under polarised light. In Plate VIII. various crystalline
and other bodies are displayed. In No. 158 is a section of new red
sandstone; 159 of quartz; and 160 of granite. Special reference is made to
others in the following list of salts and other substances which form a
beautiful series of objects for study under polarised light:—
SALTS.
Alum.
Asparagine.
Aspartic Acid. Plate VIII. No. 168.
Bitartrate of Ammonia.
Boracic Acid.
Borax. No. 164.
Carbonate of Lime.
" Soda.
Chlorate of Potash.
Chloride of Barium.
" Cobalt.
" Copper and Ammonia.
" Sodium.
Cholesterine.
Chromate of Potash.
Cinchonine.
Cinchonidine.
Citric Acid.
Hippuric Acid.
Iodide of Mercury.
" Potassium.
" Quinine.
microscope.
Among natural crystals we look for the material for the formation of our
lenses, while the varieties of granites present us with the earliest crystallised
condition of the earth’s crust as it cooled down, the structure of which is
beautifully exhibited under polarised light. In Plate VIII. various crystalline
and other bodies are displayed. In No. 158 is a section of new red
sandstone; 159 of quartz; and 160 of granite. Special reference is made to
others in the following list of salts and other substances which form a
beautiful series of objects for study under polarised light:—
SALTS.
Alum.
Asparagine.
Aspartic Acid. Plate VIII. No. 168.
Bitartrate of Ammonia.
Boracic Acid.
Borax. No. 164.
Carbonate of Lime.
" Soda.
Chlorate of Potash.
Chloride of Barium.
" Cobalt.
" Copper and Ammonia.
" Sodium.
Cholesterine.
Chromate of Potash.
Cinchonine.
Cinchonidine.
Citric Acid.
Hippuric Acid.
Iodide of Mercury.
" Potassium.
" Quinine.
Page 291
Iodo-disulphate of Quinine.
Kreatine. No. 166.
Murexide.
Nitrate of Bismuth.
" Barytes.
" Brucine.
" Copper.
" Potash.
" Strontian.
" Uranium.
Oxalate of Ammonia.
" Chromium.
" Chromium and Potash.
" Lime.
" Soda.
Indurated Sandstone, Howth.
Indurated Sandstone, Bromsgrove.
Gibraltar Rock.
Granite, various localities. No. 160.
Hornblend Schist.
Labrador Spar.
Norway Rock.
Quartz Rock, various. No. 159.
" in Bog Iron Ore.
Quartzite, Mont Blanc.
Sandstone. No. 158.
Satin Spar.
Selenites, various colours.
Tin Ore, with Tourmalin.
Oxalic Acid.
Oxalurate of Ammonia.
Permanganate of Potash.
Phosphate of Lead and Soda.
Platino-cyanide of Magnesia.
Plumose Quinidine.
Prussiate of Potash, red and yellow.
Quinidine.
Kreatine. No. 166.
Murexide.
Nitrate of Bismuth.
" Barytes.
" Brucine.
" Copper.
" Potash.
" Strontian.
" Uranium.
Oxalate of Ammonia.
" Chromium.
" Chromium and Potash.
" Lime.
" Soda.
Indurated Sandstone, Howth.
Indurated Sandstone, Bromsgrove.
Gibraltar Rock.
Granite, various localities. No. 160.
Hornblend Schist.
Labrador Spar.
Norway Rock.
Quartz Rock, various. No. 159.
" in Bog Iron Ore.
Quartzite, Mont Blanc.
Sandstone. No. 158.
Satin Spar.
Selenites, various colours.
Tin Ore, with Tourmalin.
Oxalic Acid.
Oxalurate of Ammonia.
Permanganate of Potash.
Phosphate of Lead and Soda.
Platino-cyanide of Magnesia.
Plumose Quinidine.
Prussiate of Potash, red and yellow.
Quinidine.
Page 292
Santonine.
Salicine.
Salignine. No. 162.
Sulphate of Cadmium.
" Copper. No. 161.
" Copper and Potash.
" Iron. No. 163.
" Iron and Cobalt. No. 165.
" Magnesia.
" Nickel and Potash.
" Soda.
" Zinc.
Sugar.
Tartaric Acid.
Thionurate of Ammonia.
Triple Phosphate.
Urate of Ammonia.
" Soda.
Urea, and most urinary deposits.
Uric Acid.
MINERALS.
Agates, various.
Asbestiform Serpentine.
Avanturine.
Carbonate of Lime.
Carrara Marble.
ANIMAL STRUCTURES.
Cat’s Tongue. No. 174.
Grayling Scale. No. 176.
Holothuria, Spicules of. Nos. 171-2.
Prawn Shell. No. 175.
Salicine.
Salignine. No. 162.
Sulphate of Cadmium.
" Copper. No. 161.
" Copper and Potash.
" Iron. No. 163.
" Iron and Cobalt. No. 165.
" Magnesia.
" Nickel and Potash.
" Soda.
" Zinc.
Sugar.
Tartaric Acid.
Thionurate of Ammonia.
Triple Phosphate.
Urate of Ammonia.
" Soda.
Urea, and most urinary deposits.
Uric Acid.
MINERALS.
Agates, various.
Asbestiform Serpentine.
Avanturine.
Carbonate of Lime.
Carrara Marble.
ANIMAL STRUCTURES.
Cat’s Tongue. No. 174.
Grayling Scale. No. 176.
Holothuria, Spicules of. Nos. 171-2.
Prawn Shell. No. 175.
Page 293
VEGETABLE CRYSTALLINE SUBSTANCES.
Cuticle of Leaf of Correa Cardinalis.
" " Deutzia scabra. No. 173.
" " Elæagnus.
" " Onosma taurica.
Equisetum. No. 170.
Fibro cells from orchid. No. 169.
" Oncidium bicallosum.
Scalariform Vessels from Fern.
Scyllium Caniculum. No. 177.
Silicious Cuticles, various.
Starches, various. No. 167.
The formation of artificial crystal may be readily effected, and the process
watched, under the microscope, by simply placing a drop of saturated
solution of any salt upon a previously warmed slip of glass.
Interesting results will be obtained by combining two or more chemical
salts in the following manner. To a nearly saturated solution of the sulphate
of copper and sulphate of magnesia add a drop on the glass-slide, and dry
quickly. To effect this, heat the slide so as to fuse the salts in its water of
crystallisation, and there remains an amorphous film on the hot glass. Put
the slide aside and allow it to cool slowly; it will gradually absorb a certain
amount of moisture from the air, and begin to throw out crystals. If now
placed under the microscope, numerous points will be seen to start out here
and there. The starting points may be produced at pleasure by touching the
film with a fine needle point, so as to admit of a slight amount of moisture
being absorbed by the mass of salt. Development is at once suspended by
applying gentle heat; cover the specimen with balsam and thin glass. The
balsam should completely cover the edges of the thin glass circle, otherwise
moisture will probably insinuate itself, and destroy the form of the crystals.
Mr. Thomas succeeded in crystallising “the salts of the magnetic metals” at
very high temperatures, with very curious results. In Plate VIII. are seen
crystals of sulphate of iron and cobalt, No. 163; and of nickel and potash,
No. 165, obtained in the following manner:—Add to a concentrated
Cuticle of Leaf of Correa Cardinalis.
" " Deutzia scabra. No. 173.
" " Elæagnus.
" " Onosma taurica.
Equisetum. No. 170.
Fibro cells from orchid. No. 169.
" Oncidium bicallosum.
Scalariform Vessels from Fern.
Scyllium Caniculum. No. 177.
Silicious Cuticles, various.
Starches, various. No. 167.
The formation of artificial crystal may be readily effected, and the process
watched, under the microscope, by simply placing a drop of saturated
solution of any salt upon a previously warmed slip of glass.
Interesting results will be obtained by combining two or more chemical
salts in the following manner. To a nearly saturated solution of the sulphate
of copper and sulphate of magnesia add a drop on the glass-slide, and dry
quickly. To effect this, heat the slide so as to fuse the salts in its water of
crystallisation, and there remains an amorphous film on the hot glass. Put
the slide aside and allow it to cool slowly; it will gradually absorb a certain
amount of moisture from the air, and begin to throw out crystals. If now
placed under the microscope, numerous points will be seen to start out here
and there. The starting points may be produced at pleasure by touching the
film with a fine needle point, so as to admit of a slight amount of moisture
being absorbed by the mass of salt. Development is at once suspended by
applying gentle heat; cover the specimen with balsam and thin glass. The
balsam should completely cover the edges of the thin glass circle, otherwise
moisture will probably insinuate itself, and destroy the form of the crystals.
Mr. Thomas succeeded in crystallising “the salts of the magnetic metals” at
very high temperatures, with very curious results. In Plate VIII. are seen
crystals of sulphate of iron and cobalt, No. 163; and of nickel and potash,
No. 165, obtained in the following manner:—Add to a concentrated
Page 294
solution of iron a small quantity of sugar, to prevent oxidation. Put a drop of
the solution on a glass slide, and drive out the water of crystallisation as
quickly as possible by the aid of a spirit lamp; then with a Bunsen’s burner
bring the plate to a high temperature. Immediately a remarkable change is
seen to take place in the form of the crystal, and if properly managed the
“foliation” represented in the plate will be fairly exhibited. The slide must
not be allowed to cool down too rapidly or the crystals will probably absorb
moisture from the atmosphere, and in so doing the crystals alter their forms.
Immerse them in balsam, and cover in the usual way before quite cold.
Sublimation of Alkaloids.—The late Dr. Guy, F.R.S., directed the attention
of microscopists to the fact that the crystalline shape of bodies belonging to
the inorganic world might be of service in medical jurisprudence.
Subsequently, Dr. A. Helwig, of Mayence, investigated this subject, and
found the plan applicable not only to inorganic but also to organic
substances, and especially to poisonous alkaloids. By using a white
porcelain saucer Dr. Guy was able to watch the process of crystallisation
more minutely, and to regulate it more exactly. He was, in fact, able to
obtain characteristic crusts composed of crystals of strychnine weighing not
more than 1⁄3000th or 1⁄5000th of a grain. Morphia affords equally characteristic
results. For the examination of these, Dr. Guy recommended the use of a
binocular microscope with an inch object-glass. But it is not to crystalline
forms alone that one need trust; the whole behaviour of a substance as it
melts and is converted into vapour is eminently characteristic, and when
once deposited on the microscopical slide, under the object-glass, the
application of re-agents may give still more satisfactory results. The re-
agents, however, which are here to be applied are not of the kind ordinarily
employed. Colour-tests under the microscope are, comparatively speaking,
useless; those that give rise to peculiar crystalline forms are rather to be
sought after. For instance, the crystals produced by the action of carbozotic
acid on morphia are by themselves almost perfectly characteristic. These
experiments should not, however, be undertaken for medico-legal purposes
by one unskilled in their conduct, for the effects of the reagents themselves
might be mistaken by the uninitiated for the result of their action on the
substance under examination. For the special method of procedure, see Dr.
W. Guy, “On the Sublimation of the Alkaloids.”34
the solution on a glass slide, and drive out the water of crystallisation as
quickly as possible by the aid of a spirit lamp; then with a Bunsen’s burner
bring the plate to a high temperature. Immediately a remarkable change is
seen to take place in the form of the crystal, and if properly managed the
“foliation” represented in the plate will be fairly exhibited. The slide must
not be allowed to cool down too rapidly or the crystals will probably absorb
moisture from the atmosphere, and in so doing the crystals alter their forms.
Immerse them in balsam, and cover in the usual way before quite cold.
Sublimation of Alkaloids.—The late Dr. Guy, F.R.S., directed the attention
of microscopists to the fact that the crystalline shape of bodies belonging to
the inorganic world might be of service in medical jurisprudence.
Subsequently, Dr. A. Helwig, of Mayence, investigated this subject, and
found the plan applicable not only to inorganic but also to organic
substances, and especially to poisonous alkaloids. By using a white
porcelain saucer Dr. Guy was able to watch the process of crystallisation
more minutely, and to regulate it more exactly. He was, in fact, able to
obtain characteristic crusts composed of crystals of strychnine weighing not
more than 1⁄3000th or 1⁄5000th of a grain. Morphia affords equally characteristic
results. For the examination of these, Dr. Guy recommended the use of a
binocular microscope with an inch object-glass. But it is not to crystalline
forms alone that one need trust; the whole behaviour of a substance as it
melts and is converted into vapour is eminently characteristic, and when
once deposited on the microscopical slide, under the object-glass, the
application of re-agents may give still more satisfactory results. The re-
agents, however, which are here to be applied are not of the kind ordinarily
employed. Colour-tests under the microscope are, comparatively speaking,
useless; those that give rise to peculiar crystalline forms are rather to be
sought after. For instance, the crystals produced by the action of carbozotic
acid on morphia are by themselves almost perfectly characteristic. These
experiments should not, however, be undertaken for medico-legal purposes
by one unskilled in their conduct, for the effects of the reagents themselves
might be mistaken by the uninitiated for the result of their action on the
substance under examination. For the special method of procedure, see Dr.
W. Guy, “On the Sublimation of the Alkaloids.”34
Page 295
The Micro-spectroscope.
Spectrum analysis has, from its first introduction by Kirschoff in 1859,
maintained its fascination over men of science throughout the civilised
world. Microscopists, astronomers, and chemists have assigned to the
spectroscope a highly important position amongst scientific instruments of
research. At quite an early period of its history it appeared to ourselves to
promise an extension of the work of the microscope in pathology and
microscopy, and second only to that of astronomy and chemistry. The chief
hindrances to the use of the spectroscope were, in the early days, of a
twofold nature; a widespread, but quite erroneous view of the serious
difficulties of employing the instrument, and the want of a first aid to its
use.
So valuable a means of research has this process of analysis proved to be,
that the discoveries made by the spectroscope appear marvellous. The
spectroscope was first made known as a refined instrument for the analysis
of light by two Germans, a physicist and a chemist, Kirschoff and Bunsen.
In 1860, the latter succeeded in detecting and separating two new alkaline
bodies from all other bodies from the waters obtained from the Durkeim
springs, less than 0·0002 part of a milligramme of which can be detected by
spectrum analysis. It is to the labours of Huggins, Norman Lockyer and
others that we are indebted for the wonderful discoveries made in
astronomy; and chiefly so to Brewster, Herschel, and Talbot, for showing
that certain metals give off light of a high degree of refrangibility; that
distinct bands are situated at a distance beyond the last visible violet ray ten
times as great as the length of the whole visible spectrum from red to violet.
With regard to the discoveries made in connection with physiological
research, we are indebted to F. Hoppe, who in 1862 first described the
absorption bands of human blood. His results were confirmed by the
investigations of Professor Sir George Gabriel Stokes, who, by adding
certain reducing agents to the blood, found that he could change scarlet
blood into purple—“purple cruorine”—and in this way the place occupied
by the absorption band in the spectrum could be made to change. He
reduced the hæmoglobin by robbing the blood of its oxygen. Thus, by
Stokes’ and other methods, we have since arrived at extremely valuable
Spectrum analysis has, from its first introduction by Kirschoff in 1859,
maintained its fascination over men of science throughout the civilised
world. Microscopists, astronomers, and chemists have assigned to the
spectroscope a highly important position amongst scientific instruments of
research. At quite an early period of its history it appeared to ourselves to
promise an extension of the work of the microscope in pathology and
microscopy, and second only to that of astronomy and chemistry. The chief
hindrances to the use of the spectroscope were, in the early days, of a
twofold nature; a widespread, but quite erroneous view of the serious
difficulties of employing the instrument, and the want of a first aid to its
use.
So valuable a means of research has this process of analysis proved to be,
that the discoveries made by the spectroscope appear marvellous. The
spectroscope was first made known as a refined instrument for the analysis
of light by two Germans, a physicist and a chemist, Kirschoff and Bunsen.
In 1860, the latter succeeded in detecting and separating two new alkaline
bodies from all other bodies from the waters obtained from the Durkeim
springs, less than 0·0002 part of a milligramme of which can be detected by
spectrum analysis. It is to the labours of Huggins, Norman Lockyer and
others that we are indebted for the wonderful discoveries made in
astronomy; and chiefly so to Brewster, Herschel, and Talbot, for showing
that certain metals give off light of a high degree of refrangibility; that
distinct bands are situated at a distance beyond the last visible violet ray ten
times as great as the length of the whole visible spectrum from red to violet.
With regard to the discoveries made in connection with physiological
research, we are indebted to F. Hoppe, who in 1862 first described the
absorption bands of human blood. His results were confirmed by the
investigations of Professor Sir George Gabriel Stokes, who, by adding
certain reducing agents to the blood, found that he could change scarlet
blood into purple—“purple cruorine”—and in this way the place occupied
by the absorption band in the spectrum could be made to change. He
reduced the hæmoglobin by robbing the blood of its oxygen. Thus, by
Stokes’ and other methods, we have since arrived at extremely valuable
Page 296
results, and the explanation of the difference in colour between arterial and
venous blood; and it has also enabled us to show wherein the breathing
power of the red corpuscles resides, and further explains phenomena which
before his investigations were inexplicable.
venous blood; and it has also enabled us to show wherein the breathing
power of the red corpuscles resides, and further explains phenomena which
before his investigations were inexplicable.
Page 297
Fig. 191.—Fräunhofer’s Spectrum Lines.
The spectroscope seems likely to be of almost as great use in medicine as it
has already proved to be in solar and terrestrial chemistry, if we may form
an opinion from the large amount of literature which has appeared on the
subject. The inception of this magical instrument arose on the instance of a
discovery made by Dr. Wollaston in 1802, who, on making a slit in the
shutter of his room, instead of a round hole, the spectrum of sunlight,
instead of being composed of a number of coloured discs, was now a band
of pure colours, each colour being free from admixture with the next to it.
Moreover, he found that this colour band was not continuous, as Newton
described it, but interrupted here and there by fine black lines.
In 1814, Fräunhofer,35 a German optician, discovered these lines quite
independently, and mapped out 576 of them, calling the more prominent of
them A, B, C, D, E, F, G, H, which lines he used as marks of comparison.
He also found that the distances of these lines from each other may vary
according to the nature of the substance composing the prism; thus, their
relative distances are not the same in prisms of flint-glass, crown-glass, and
bisulphide of carbon, but they always occupy the same position relatively to
the colours of the spectrum. Kirschoff and Angström had mapped out in
1880 no less a number than 2,000 Fräunhofer lines, a portion of which are
correctly shown in the accompanying chart (Fig. 191).
In 1830, Simms, a London optician, made an improvement in the
construction of the spectroscope by placing a lens in front of the prism, so
arranged that the slit was in the focus of the lens. This lens turns the light,
after it has passed through the slit, into a cylindrical beam before entering
the prism. Another lens, also introduced by him, receives the circular beam
The spectroscope seems likely to be of almost as great use in medicine as it
has already proved to be in solar and terrestrial chemistry, if we may form
an opinion from the large amount of literature which has appeared on the
subject. The inception of this magical instrument arose on the instance of a
discovery made by Dr. Wollaston in 1802, who, on making a slit in the
shutter of his room, instead of a round hole, the spectrum of sunlight,
instead of being composed of a number of coloured discs, was now a band
of pure colours, each colour being free from admixture with the next to it.
Moreover, he found that this colour band was not continuous, as Newton
described it, but interrupted here and there by fine black lines.
In 1814, Fräunhofer,35 a German optician, discovered these lines quite
independently, and mapped out 576 of them, calling the more prominent of
them A, B, C, D, E, F, G, H, which lines he used as marks of comparison.
He also found that the distances of these lines from each other may vary
according to the nature of the substance composing the prism; thus, their
relative distances are not the same in prisms of flint-glass, crown-glass, and
bisulphide of carbon, but they always occupy the same position relatively to
the colours of the spectrum. Kirschoff and Angström had mapped out in
1880 no less a number than 2,000 Fräunhofer lines, a portion of which are
correctly shown in the accompanying chart (Fig. 191).
In 1830, Simms, a London optician, made an improvement in the
construction of the spectroscope by placing a lens in front of the prism, so
arranged that the slit was in the focus of the lens. This lens turns the light,
after it has passed through the slit, into a cylindrical beam before entering
the prism. Another lens, also introduced by him, receives the circular beam
Page 298
emerging from the prism, and compels it to throw an image of the slit,
which may be magnified at pleasure for each ray. The lens between the
prism and the slit is termed the collimating lens. Thus the following are the
essential parts of a chemical spectroscope:—(1) a slit, the edges of which
are two knife-edges of steel very truly ground, and exactly parallel to each
other, and in a direction parallel to the refracting edge of the prism, to admit
a pencil of rays. (2) A collimating lens; a convex lens with the slit at its
principal focus, which renders the rays parallel before entering the prism.
(3) A prism of dense glass, in which the rays are refracted and dispersed. (4)
An observing telescope constructed like an astronomical refractor of small
size, and placed so that the rays shall traverse it after emerging from the
prism. Such are the essentials of a one-prism chemical spectroscope.
The form of instrument in use with the microscope is the “direct vision”
spectroscope, consisting of two prisms of flint-glass, placed between three
of crown-glass cemented together by Canada balsam; the spectrum being
viewed directly by the eye. The earliest constructed form of micro-
spectroscope is shown in Fig. 192, the Browning-Huggins.
It was, however, Mr. Sorby who suggested that the prism should be made of
dense flint-glass and of such a form that it could be used in two different
positions, and that in one it should give twice the dispersion that it would in
the other, but that the angle made by the incident and emergent rays should
be the same in both positions.
which may be magnified at pleasure for each ray. The lens between the
prism and the slit is termed the collimating lens. Thus the following are the
essential parts of a chemical spectroscope:—(1) a slit, the edges of which
are two knife-edges of steel very truly ground, and exactly parallel to each
other, and in a direction parallel to the refracting edge of the prism, to admit
a pencil of rays. (2) A collimating lens; a convex lens with the slit at its
principal focus, which renders the rays parallel before entering the prism.
(3) A prism of dense glass, in which the rays are refracted and dispersed. (4)
An observing telescope constructed like an astronomical refractor of small
size, and placed so that the rays shall traverse it after emerging from the
prism. Such are the essentials of a one-prism chemical spectroscope.
The form of instrument in use with the microscope is the “direct vision”
spectroscope, consisting of two prisms of flint-glass, placed between three
of crown-glass cemented together by Canada balsam; the spectrum being
viewed directly by the eye. The earliest constructed form of micro-
spectroscope is shown in Fig. 192, the Browning-Huggins.
It was, however, Mr. Sorby who suggested that the prism should be made of
dense flint-glass and of such a form that it could be used in two different
positions, and that in one it should give twice the dispersion that it would in
the other, but that the angle made by the incident and emergent rays should
be the same in both positions.
Page 299
Fig. 192.—The Browning-Huggins Micro-spectroscope.
Fig. 193. Fig. 193a.
Figs. 193 and 193a represent prisms of the kind arranged to use in two
different positions, i and i′ being the same angle as I and I′.
For most absorption-bands, particularly if faint, the prism should be used in
the first position, in which it gives the least dispersion; when greater
dispersion is required, so as to separate some particular lines more widely,
or to show the spectra of the metals, or Fräunhofer’s lines in the solar
spectrum, then the prism must be used as in Fig. 193a. This answers well
for liquids or transparent objects, but it is, of course, not applicable to
opaque objects.
To combine both purposes, some form of direct vision-prisms that maybe
applied to the body of the microscope is required. Fig. 194 represents an
arrangement of direct vision-prisms, invented by Herschel. The line R R′
shows the path of a ray of light through the prisms, where it would be seen
that the emergent ray R′ is parallel and coincident with the incident ray R.
Another very compact combination is shown in Fig. 194a. Any number of
these prisms (P P P) may be used, according to the amount of dispersion
required. They are mounted in a similar way to a Nicol’s prism, and are
applied directly over the eye-piece of the microscope. The slit S S is placed
in the focus of the first glass (F) if a negative, or below the second glass if a
positive eye-piece be employed. One edge of the slit is movable, and, in
using the instrument, the slit is first opened wide, so that a clear view of the
object is obtained. The part of the object of which the spectrum is to be
Fig. 193. Fig. 193a.
Figs. 193 and 193a represent prisms of the kind arranged to use in two
different positions, i and i′ being the same angle as I and I′.
For most absorption-bands, particularly if faint, the prism should be used in
the first position, in which it gives the least dispersion; when greater
dispersion is required, so as to separate some particular lines more widely,
or to show the spectra of the metals, or Fräunhofer’s lines in the solar
spectrum, then the prism must be used as in Fig. 193a. This answers well
for liquids or transparent objects, but it is, of course, not applicable to
opaque objects.
To combine both purposes, some form of direct vision-prisms that maybe
applied to the body of the microscope is required. Fig. 194 represents an
arrangement of direct vision-prisms, invented by Herschel. The line R R′
shows the path of a ray of light through the prisms, where it would be seen
that the emergent ray R′ is parallel and coincident with the incident ray R.
Another very compact combination is shown in Fig. 194a. Any number of
these prisms (P P P) may be used, according to the amount of dispersion
required. They are mounted in a similar way to a Nicol’s prism, and are
applied directly over the eye-piece of the microscope. The slit S S is placed
in the focus of the first glass (F) if a negative, or below the second glass if a
positive eye-piece be employed. One edge of the slit is movable, and, in
using the instrument, the slit is first opened wide, so that a clear view of the
object is obtained. The part of the object of which the spectrum is to be
Page 300
examined is then made to
coincide with the fixed edge of
the slit, and the movable edge is
screwed up, until a brilliant
coloured spectrum is produced.
The absorption-bands will then
be readily found by slightly
altering the focus. This
contrivance answers perfectly
for opaque objects, without any
preparation; and, when
desirable, the same prism can be
placed below the stage, and a
micrometer used in the eye-
piece of the microscope, thus
avoiding a multiplicity of
apparatus.
Fig. 194. Fig. 194a.
A later and better form of
instrument is the Sorby-Browning
eye-piece (Fig. 195), shown in
section (Fig. 196) ready for inserting
into the body-tube of the microscope,
the prism of which is contained in a
small tube, removable at pleasure.
Below the prism is an achromatic
eye-piece, having an adjustable slit
between the two lenses, the upper
lens being furnished with a screw
motion to focus the slit. A side slit,
capable of adjustment, admits, when
Fig. 195.—The Sorby-Browning Micro-
required, a second beam of light spectroscopic Eye-piece.
from any object whose spectrum it is
desired to compare with that of the object placed on the stage of the
microscope. This second beam of light strikes against a very small prism,
suitably placed inside the apparatus, and is reflected up through the
coincide with the fixed edge of
the slit, and the movable edge is
screwed up, until a brilliant
coloured spectrum is produced.
The absorption-bands will then
be readily found by slightly
altering the focus. This
contrivance answers perfectly
for opaque objects, without any
preparation; and, when
desirable, the same prism can be
placed below the stage, and a
micrometer used in the eye-
piece of the microscope, thus
avoiding a multiplicity of
apparatus.
Fig. 194. Fig. 194a.
A later and better form of
instrument is the Sorby-Browning
eye-piece (Fig. 195), shown in
section (Fig. 196) ready for inserting
into the body-tube of the microscope,
the prism of which is contained in a
small tube, removable at pleasure.
Below the prism is an achromatic
eye-piece, having an adjustable slit
between the two lenses, the upper
lens being furnished with a screw
motion to focus the slit. A side slit,
capable of adjustment, admits, when
Fig. 195.—The Sorby-Browning Micro-
required, a second beam of light spectroscopic Eye-piece.
from any object whose spectrum it is
desired to compare with that of the object placed on the stage of the
microscope. This second beam of light strikes against a very small prism,
suitably placed inside the apparatus, and is reflected up through the
Page 301
compound prism, forming a spectrum in the same field with that obtained
from the object on the stage.
A is a brass tube, carrying the
compound direct vision prism; B, a
milled head, with screw motion to
adjust the focus of the achromatic
eye lens C, seen in the sectional view
as a triple combination of prisms.
Another screw at right angles to C,
which from its position cannot be
well shown in the figure, regulates
the slit horizontally. This screw has a
larger head, and when once
recognised cannot be mistaken for
the other. D D is a clip and ledge for
holding a small tube, so that the
spectrum given by its contents may
be compared with one from an object
on the stage. E is a round hole for a
square-headed screw, opening and
shutting a slit, admitting the quantity
of light required to form the second
spectrum. A light entering the round
Fig. 196.—Sectional view of bright-line hole near E strikes against the right-
Spectroscope; the letters also apply to the angled prism, which is placed inside
standard spectrum scale (Fig. 198).
the apparatus, and is reflected up
through the slit belonging to the
compound prism. If any incandescent object be placed in a suitable position
with reference to the round hole, its spectrum will be obtained. F shows the
position of the field lens of the eye-piece. The tube is made to fit the
microscope to which the instrument is applied. To use this instrument insert
F as an eye-piece in the microscope tube, taking care that the slit at the top
of the eye-piece is in the same direction as the slit below the prism. Screw
on to the microscope the object-glass required, and place the object whose
spectrum is to be viewed on the stage. Illuminate with the stage mirror if it
be transparent; with mirror, Lieberkühn, and dark well, by side reflector, or
from the object on the stage.
A is a brass tube, carrying the
compound direct vision prism; B, a
milled head, with screw motion to
adjust the focus of the achromatic
eye lens C, seen in the sectional view
as a triple combination of prisms.
Another screw at right angles to C,
which from its position cannot be
well shown in the figure, regulates
the slit horizontally. This screw has a
larger head, and when once
recognised cannot be mistaken for
the other. D D is a clip and ledge for
holding a small tube, so that the
spectrum given by its contents may
be compared with one from an object
on the stage. E is a round hole for a
square-headed screw, opening and
shutting a slit, admitting the quantity
of light required to form the second
spectrum. A light entering the round
Fig. 196.—Sectional view of bright-line hole near E strikes against the right-
Spectroscope; the letters also apply to the angled prism, which is placed inside
standard spectrum scale (Fig. 198).
the apparatus, and is reflected up
through the slit belonging to the
compound prism. If any incandescent object be placed in a suitable position
with reference to the round hole, its spectrum will be obtained. F shows the
position of the field lens of the eye-piece. The tube is made to fit the
microscope to which the instrument is applied. To use this instrument insert
F as an eye-piece in the microscope tube, taking care that the slit at the top
of the eye-piece is in the same direction as the slit below the prism. Screw
on to the microscope the object-glass required, and place the object whose
spectrum is to be viewed on the stage. Illuminate with the stage mirror if it
be transparent; with mirror, Lieberkühn, and dark well, by side reflector, or
Page 302
bull’s-eye condenser if opaque. Remove A, and open the slit by means of
the milled-head, not shown in figure, but which is at right angles to D D.
When the slit is sufficiently open the rest of the apparatus acts as an
ordinary eye-piece, and any object can be focussed in the usual way. Having
focussed the object, replace A, and gradually close the slit till a good
spectrum is obtained. The spectrum will be much improved by throwing the
object a little out of focus.
Sectional View.
Figs. 197 and 197a.—The Beck-Sorby Micro-spectroscope Eye-piece, drawn on a
scale of one half size.
Every part of the spectrum differs a little from adjacent parts in
refrangibility, and delicate bands or lines can only be brought out by
accurately focussing that particular part of the spectrum. This can be done
by the milled-head B. Disappointment will occur in any attempt at delicate
investigation if the directions given be not carefully followed out.
Opposite E a small mirror is attached. It is like the mirror below the stage of
a microscope, and is mounted in a similar manner. By means of this mirror
the milled-head, not shown in figure, but which is at right angles to D D.
When the slit is sufficiently open the rest of the apparatus acts as an
ordinary eye-piece, and any object can be focussed in the usual way. Having
focussed the object, replace A, and gradually close the slit till a good
spectrum is obtained. The spectrum will be much improved by throwing the
object a little out of focus.
Sectional View.
Figs. 197 and 197a.—The Beck-Sorby Micro-spectroscope Eye-piece, drawn on a
scale of one half size.
Every part of the spectrum differs a little from adjacent parts in
refrangibility, and delicate bands or lines can only be brought out by
accurately focussing that particular part of the spectrum. This can be done
by the milled-head B. Disappointment will occur in any attempt at delicate
investigation if the directions given be not carefully followed out.
Opposite E a small mirror is attached. It is like the mirror below the stage of
a microscope, and is mounted in a similar manner. By means of this mirror
Page 303
light may be reflected into the eye-piece, and in this way two spectra may
be procured from one lamp.
Method of using the Micro-Spectroscope.
A beginner with the micro-spectroscope should first make himself fully
acquainted with the spectroscope by holding it up to the sky and noting the
effects of opening and regulating the slit, by rotating the screw C, Figs. 195
and 197. The lines will be well seen on closing down the opening. This
screw diminishes the length of the slit, when the spectrum is seen as a
narrow ribbon of prismatic colours. The screw E regulates the admission of
light through the aperture above D. The better objects with which to
commence the study of the absorption bands are, aniline dye, much diluted,
madder, permanganate of potash, and blood. As each colour varies in
refrangibility, the focus must be adjusted by the screw E. When it is desired
to view the spectrum of a very minute object, the prisms should be removed
by withdrawing the tube containing them, the slit set open, and the object
brought into the centre of the field; the vertical and horizontal slits must
then be partially closed up, and the prisms replaced, when a suitable
objective is employed to examine the spectrum. For ordinary observations a
magnifying power of an inch and a half or two inches will be suitable, but
for small quantities of material a higher power must be employed, when a
single blood corpuscle can be made to show its characteristic absorption
band. After having obtained the best image of any object on stage, throw it
slightly out of focus, and substitute the micro-spectroscopic eye-piece for
the Huyghenian. Opaque objects should be examined by reflected light, by
means of the bull’s-eye condenser, or side reflector. Mr. Sorby uses a
binocular microscope, which enables him to regulate the focussing and
throwing out of focus of the object.
In examining crystals or other small objects, a small cardboard diaphragm
should be placed beneath them; and when examining the spectra of liquids
in cells, slip a small cap with a perforation of 1⁄10-inch in diameter over the
tube containing the ½-inch or 2-inch objective. Substances which give
absorption bands or lines in the red are best seen by artificial light, while
those which show bands in the violet are better seen by daylight. By
be procured from one lamp.
Method of using the Micro-Spectroscope.
A beginner with the micro-spectroscope should first make himself fully
acquainted with the spectroscope by holding it up to the sky and noting the
effects of opening and regulating the slit, by rotating the screw C, Figs. 195
and 197. The lines will be well seen on closing down the opening. This
screw diminishes the length of the slit, when the spectrum is seen as a
narrow ribbon of prismatic colours. The screw E regulates the admission of
light through the aperture above D. The better objects with which to
commence the study of the absorption bands are, aniline dye, much diluted,
madder, permanganate of potash, and blood. As each colour varies in
refrangibility, the focus must be adjusted by the screw E. When it is desired
to view the spectrum of a very minute object, the prisms should be removed
by withdrawing the tube containing them, the slit set open, and the object
brought into the centre of the field; the vertical and horizontal slits must
then be partially closed up, and the prisms replaced, when a suitable
objective is employed to examine the spectrum. For ordinary observations a
magnifying power of an inch and a half or two inches will be suitable, but
for small quantities of material a higher power must be employed, when a
single blood corpuscle can be made to show its characteristic absorption
band. After having obtained the best image of any object on stage, throw it
slightly out of focus, and substitute the micro-spectroscopic eye-piece for
the Huyghenian. Opaque objects should be examined by reflected light, by
means of the bull’s-eye condenser, or side reflector. Mr. Sorby uses a
binocular microscope, which enables him to regulate the focussing and
throwing out of focus of the object.
In examining crystals or other small objects, a small cardboard diaphragm
should be placed beneath them; and when examining the spectra of liquids
in cells, slip a small cap with a perforation of 1⁄10-inch in diameter over the
tube containing the ½-inch or 2-inch objective. Substances which give
absorption bands or lines in the red are best seen by artificial light, while
those which show bands in the violet are better seen by daylight. By
Page 304
following rules of the kind we are less likely to mix the bands of the
absorption spectrum with the Fräunhofer lines. For example, if the edge of a
band happens to coincide with a Fräunhofer line, the observer is apt to
imagine that the band is better defined and more abruptly shaded on one
side than it really is.
Standard Spectrum
Scale. Cells for use with Spectroscope.
Fig. 198.
Cells and Tubes.—These are either supplied ready-made by the optician, or
can be formed out of small pieces of barometer tubing, with the edges
ground down and cemented on ordinary glass slips. In Fig. 198 is seen the
several kinds of cells and tubes usually employed, while the little flat tubes
commonly in use as bouquet holders will be found of use, with the side
stage reflecting spectrum as comparison tubes; being of different diameters
they allow of two or more depths of colour in the fluid intended for
examination.
In the case of many other fluids the sloping form of cell (Fig. 198) will be
useful, as different shades of fluids can be examined without removal from
the stage of the microscope. The deeper cells are cut from a piece of
barometer tubing of about half to an inch long, one end being cemented to a
piece of flatted glass, and the other covered over temporarily or
permanently with a thin piece of glass on the top, held in its place by
capillary attraction, thus admitting of the tube being turned upside down.
Re-agents required.—A diluted solution of ammonia, citric acid, double
tartrate of potash and soda (the last being used to prevent the precipitation
absorption spectrum with the Fräunhofer lines. For example, if the edge of a
band happens to coincide with a Fräunhofer line, the observer is apt to
imagine that the band is better defined and more abruptly shaded on one
side than it really is.
Standard Spectrum
Scale. Cells for use with Spectroscope.
Fig. 198.
Cells and Tubes.—These are either supplied ready-made by the optician, or
can be formed out of small pieces of barometer tubing, with the edges
ground down and cemented on ordinary glass slips. In Fig. 198 is seen the
several kinds of cells and tubes usually employed, while the little flat tubes
commonly in use as bouquet holders will be found of use, with the side
stage reflecting spectrum as comparison tubes; being of different diameters
they allow of two or more depths of colour in the fluid intended for
examination.
In the case of many other fluids the sloping form of cell (Fig. 198) will be
useful, as different shades of fluids can be examined without removal from
the stage of the microscope. The deeper cells are cut from a piece of
barometer tubing of about half to an inch long, one end being cemented to a
piece of flatted glass, and the other covered over temporarily or
permanently with a thin piece of glass on the top, held in its place by
capillary attraction, thus admitting of the tube being turned upside down.
Re-agents required.—A diluted solution of ammonia, citric acid, double
tartrate of potash and soda (the last being used to prevent the precipitation
Page 305
of oxide of iron), and the double sulphate of the protoxide of iron and
ammonia (employed to deoxidise blood, etc.). In some special cases, dilute
hydrochloric acid, purified boric acid, and sulphate of soda are required.
The character of stains of blood varies with age and with the nature of the
substance with which it happens to be combined. This is important to
remember in connection with Jurisprudence, when the micro-spectroscope
is brought into use for the detection of blood stains. The spectrum used in
important cases of the kind should have a compound prism, with enough,
but not too great dispersive power, otherwise the bands become, as it were,
diluted, and less distinct.
If the blood stain is quite recent, the colouring matter will be hæmoglobin
only. This easily dissolves out in water, and when sufficiently diluted gives
the spectrum of oxy-hæmoglobin, which on the addition of ammonia,
together with a small quantity of the double tartrate, a small piece of ferrous
salt, and stirring carefully without the admission of air, changes the
spectrum of reduced hæmoglobin. When stirred again, so as to expose the
solution as much as possible to air, the two bands reappear; on gradually
adding citric acid in small quantities the colour begins to change, and the
bands are seen to gradually fade away; if there should have been much
blood present, a band appears in the red; the further addition of ammonia
makes all clear again, but does not restore the original bands, because the
hæmoglobin has been permanently changed into hæmatin. This reaction
alone distinguishes blood from most other colouring matters, since other
substances after being changed by acids are restored by alkalies to their
original state. There are many other curious facts connected with the
spectroscopic analysis of blood, which are fully explained and illustrated by
Dr. Maemunn in his book on “The Use of the Spectroscope in Medicine,”
and also in Dr. Thudicum’s36 reports and charts, which are the most
complete. Sir George Stokes, F.R.S., was one of the first to show the
essential value of the spectral phenomena of hematine, and who proved,
after Hoppe had first drawn attention to the fact, that this colouring matter
is capable of existing in two states of oxidation, and that a very different
spectrum is produced according as the substance, which he termed
cruorine, is in a more or less oxidised condition. The chart appended to his
ammonia (employed to deoxidise blood, etc.). In some special cases, dilute
hydrochloric acid, purified boric acid, and sulphate of soda are required.
The character of stains of blood varies with age and with the nature of the
substance with which it happens to be combined. This is important to
remember in connection with Jurisprudence, when the micro-spectroscope
is brought into use for the detection of blood stains. The spectrum used in
important cases of the kind should have a compound prism, with enough,
but not too great dispersive power, otherwise the bands become, as it were,
diluted, and less distinct.
If the blood stain is quite recent, the colouring matter will be hæmoglobin
only. This easily dissolves out in water, and when sufficiently diluted gives
the spectrum of oxy-hæmoglobin, which on the addition of ammonia,
together with a small quantity of the double tartrate, a small piece of ferrous
salt, and stirring carefully without the admission of air, changes the
spectrum of reduced hæmoglobin. When stirred again, so as to expose the
solution as much as possible to air, the two bands reappear; on gradually
adding citric acid in small quantities the colour begins to change, and the
bands are seen to gradually fade away; if there should have been much
blood present, a band appears in the red; the further addition of ammonia
makes all clear again, but does not restore the original bands, because the
hæmoglobin has been permanently changed into hæmatin. This reaction
alone distinguishes blood from most other colouring matters, since other
substances after being changed by acids are restored by alkalies to their
original state. There are many other curious facts connected with the
spectroscopic analysis of blood, which are fully explained and illustrated by
Dr. Maemunn in his book on “The Use of the Spectroscope in Medicine,”
and also in Dr. Thudicum’s36 reports and charts, which are the most
complete. Sir George Stokes, F.R.S., was one of the first to show the
essential value of the spectral phenomena of hematine, and who proved,
after Hoppe had first drawn attention to the fact, that this colouring matter
is capable of existing in two states of oxidation, and that a very different
spectrum is produced according as the substance, which he termed
cruorine, is in a more or less oxidised condition. The chart appended to his
Page 306
paper37 affords an imperfect representation of the changes seen in the
spectrum.
No. 1.—Arterial Blood, Scarlet Cruorine.
No. 2.—Venous Blood, Purple Cruorine.
No. 3.—Blood treated with Acetic Acid.
No. 4.—Solution of Hæmatin.
Fig. 199.—Sir George Stokes’ Chart of the Absorption Bands of Blood.
Proto-sulphate of iron, or proto-chloride of tin, causes the reduction of the
colouring-matter, but, on exposure to air, oxygen is absorbed, and the
solution again exhibits the spectrum characteristic of the more oxidised
spectrum.
No. 1.—Arterial Blood, Scarlet Cruorine.
No. 2.—Venous Blood, Purple Cruorine.
No. 3.—Blood treated with Acetic Acid.
No. 4.—Solution of Hæmatin.
Fig. 199.—Sir George Stokes’ Chart of the Absorption Bands of Blood.
Proto-sulphate of iron, or proto-chloride of tin, causes the reduction of the
colouring-matter, but, on exposure to air, oxygen is absorbed, and the
solution again exhibits the spectrum characteristic of the more oxidised
Page 307
state. The different substances obtained from blood colouring-matter
produce different bands. Thus, hæmatin gives rise to a band in the red
spectrum D; hæmato-globulin produces two bands, the second twice the
breadth of the first in the yellow portion of the spectrum between the lines D
and E, No. 1. The absorption-bands differ according to the strength of the
solution employed, and the medium in which the blood-salt is dissolved;
but an exceedingly minute proportion dissolved in water is sufficient to
bring out very distinct bands. B represents the red end of the spectrum and G
the green as it approaches the violet end.
Mapping the Spectra.—In the sectional view given of the micro-
spectroscope (Fig. 196), the internal construction of the instrument is
shown, and the arrangement made for throwing a bright point on to the
surface of the upper prism is clearly seen. The mapping out is accomplished
by means of a photographic scale fixed as a standard spectrum (Fig. 198), in
the position of A A, illuminated by the small mirror at R, and focussed by a
small lens at C, so that on looking into the instrument one can see the
spectrum accurately divided into one hundred equal parts, and scale
readings can be made at once; the only precaution needed is to be sure the D
(or the sodium line, if D cannot be got) always stands at the same number on
the scale. To map absorption spectra on this scale we have to lay down a
line, as many millimetres long as there are divisions in the scale, and mark
the position of the bands on this line. Mr. Browning supplies scales printed
off ready for use. But the mapping out of spectra, as Mr. Sorby pointed out,
requires some consideration; since the number of divisions depends on the
thickness of the interference-plate, it becomes necessary to decide what
number should be adopted. Ten it was thought would be most suitable; but,
on trial, it appeared to be too few for practical work. Twenty is too many,
since it then becomes extremely difficult to count them. Twelve is as many
as can well be counted; it is a number easily remembered, is sufficiently
accurate, and has other practical advantages. With twelve divisions the
sodium-line 0 comes very accurately at 3½; thus, by adjusting the plate so
that a bright sodium-light is brought into the centre of the band, when the
Nicol’s prisms are also crossed accurately at 3½, parallelism is secured,
together with a wider field of observation. The general character of the
scale will be best understood from the following figure, in which the bands
are numbered, and given below the principal Fräunhofer lines. The centre of
produce different bands. Thus, hæmatin gives rise to a band in the red
spectrum D; hæmato-globulin produces two bands, the second twice the
breadth of the first in the yellow portion of the spectrum between the lines D
and E, No. 1. The absorption-bands differ according to the strength of the
solution employed, and the medium in which the blood-salt is dissolved;
but an exceedingly minute proportion dissolved in water is sufficient to
bring out very distinct bands. B represents the red end of the spectrum and G
the green as it approaches the violet end.
Mapping the Spectra.—In the sectional view given of the micro-
spectroscope (Fig. 196), the internal construction of the instrument is
shown, and the arrangement made for throwing a bright point on to the
surface of the upper prism is clearly seen. The mapping out is accomplished
by means of a photographic scale fixed as a standard spectrum (Fig. 198), in
the position of A A, illuminated by the small mirror at R, and focussed by a
small lens at C, so that on looking into the instrument one can see the
spectrum accurately divided into one hundred equal parts, and scale
readings can be made at once; the only precaution needed is to be sure the D
(or the sodium line, if D cannot be got) always stands at the same number on
the scale. To map absorption spectra on this scale we have to lay down a
line, as many millimetres long as there are divisions in the scale, and mark
the position of the bands on this line. Mr. Browning supplies scales printed
off ready for use. But the mapping out of spectra, as Mr. Sorby pointed out,
requires some consideration; since the number of divisions depends on the
thickness of the interference-plate, it becomes necessary to decide what
number should be adopted. Ten it was thought would be most suitable; but,
on trial, it appeared to be too few for practical work. Twenty is too many,
since it then becomes extremely difficult to count them. Twelve is as many
as can well be counted; it is a number easily remembered, is sufficiently
accurate, and has other practical advantages. With twelve divisions the
sodium-line 0 comes very accurately at 3½; thus, by adjusting the plate so
that a bright sodium-light is brought into the centre of the band, when the
Nicol’s prisms are also crossed accurately at 3½, parallelism is secured,
together with a wider field of observation. The general character of the
scale will be best understood from the following figure, in which the bands
are numbered, and given below the principal Fräunhofer lines. The centre of
Page 308
the bands is black, and they are shaded off gradually at each side, so that the
shaded part is about equal to the intermediate bright spaces. Taking, then,
the centres of the black bands as 1, 2, 3, &c., the centres of the spaces are
1½, 2½, 3½, &c., the lower edges of each ¾, 1¾, &c., and the upper 1¼,
2¼, &c., we can easily divide these quarters into eighths by the eye: and
this is as near as is required in the subject before us, and corresponds as
nearly as possible to 1⁄100th part of the whole spectrum, visible under
ordinary circumstances by gaslight and daylight. Absorption-bands at the
red end are best seen by lamp-light, and those at the blue end by daylight.
(Red end.) (Bue end.)
Fig. 200.—
On this scale the position of some of the principal lines of the solar
spectrum is about as follows:—
A ¾ B 1½ C 23⁄8 D 3½
E 511⁄16 b 63⁄16 F 7½ G 105⁄8
At first plates of selenite, which are easily prepared, were used, because
they can be split to nearly the requisite thickness with parallel faces; but
their depolarising power varied much with temperature. Even the ordinary
atmospheric changes alter the position of the bands. However, quartz cut
parallel to the principal axis of the crystal is but slightly affected, and is not
open to the same objection; but this is prepared with some difficulty. The
sides should be perfectly parallel, the thickness about ·043-inch, and
gradually polished down with rouge until the sodium-line is seen in its
proper place. This must be done with care, since a difference of 1⁄10000-inch
in thickness would make it almost worthless.
shaded part is about equal to the intermediate bright spaces. Taking, then,
the centres of the black bands as 1, 2, 3, &c., the centres of the spaces are
1½, 2½, 3½, &c., the lower edges of each ¾, 1¾, &c., and the upper 1¼,
2¼, &c., we can easily divide these quarters into eighths by the eye: and
this is as near as is required in the subject before us, and corresponds as
nearly as possible to 1⁄100th part of the whole spectrum, visible under
ordinary circumstances by gaslight and daylight. Absorption-bands at the
red end are best seen by lamp-light, and those at the blue end by daylight.
(Red end.) (Bue end.)
Fig. 200.—
On this scale the position of some of the principal lines of the solar
spectrum is about as follows:—
A ¾ B 1½ C 23⁄8 D 3½
E 511⁄16 b 63⁄16 F 7½ G 105⁄8
At first plates of selenite, which are easily prepared, were used, because
they can be split to nearly the requisite thickness with parallel faces; but
their depolarising power varied much with temperature. Even the ordinary
atmospheric changes alter the position of the bands. However, quartz cut
parallel to the principal axis of the crystal is but slightly affected, and is not
open to the same objection; but this is prepared with some difficulty. The
sides should be perfectly parallel, the thickness about ·043-inch, and
gradually polished down with rouge until the sodium-line is seen in its
proper place. This must be done with care, since a difference of 1⁄10000-inch
in thickness would make it almost worthless.
Page 309
The two Nicol’s prisms and the intervening plate are mounted in a tube, and
attached to a piece of brass in such a manner that the centre of the aperture
exactly corresponds to the centre of any of the cells used in the
experiments, and must be made to correspond with equal care, so that any
of them, or this apparatus in particular, may be placed on the stage and in
proper position without further adjustment, whereby both time and trouble
are saved.
Absorption Spectrum of Chromule.
In 1869 I published in the Journal of the Royal Microscopical Society38 a
paper on results obtained by the spectrum analysis of the colouring-matter
of plants and flowers, some of which were of considerable interest in many
respects. My examinations extended to several hundred different specimens,
from which I was led to conclude that the chromule of flowers is, for the
most part, due to the chemical action of the actinic rays of light over the
protoplasm of the plant, more so than to that of soil. But as certain roots of
plants, as those of the alkanet, yield their colouring-matter to oil, and in a
much smaller degree to spirit or water, it follows then that conclusions of
any kind can only be drawn after a long and careful study of the question.
Some of the results obtained were, however, of some interest at the time,
that, for example, seen in three different solutions of the chlorophyll of
Cinchona succirubra, one of three solutions in alcohol, scarcely coloured,
having in fact only a faint tinge of green colour, and the spectrum of which
much astonished me at the time. It gave four well-marked absorption-bands;
one deep sharp line in the red; another, rather narrower, in the orange,
coincident with D, or the sodium-line; one in the green, about b, coincident
with the Thallium green band; and a fourth on the blue line F, nearly as
broad as that in the red. The ethereal solution gave different results. It
showed only three bands of absorption, nearly the same as in the last case
(though all of them fainter); but the fourth in the blue was not apparent, the
whole of that end of the spectrum being absorbed a little beyond the green
line b. This solution was deep emerald-green, and even dilution did not
alter the phenomena. The acid alcoholic solution was as deeply green as the
last, but gave only the sharp broad absorption-band in the red, and two very
attached to a piece of brass in such a manner that the centre of the aperture
exactly corresponds to the centre of any of the cells used in the
experiments, and must be made to correspond with equal care, so that any
of them, or this apparatus in particular, may be placed on the stage and in
proper position without further adjustment, whereby both time and trouble
are saved.
Absorption Spectrum of Chromule.
In 1869 I published in the Journal of the Royal Microscopical Society38 a
paper on results obtained by the spectrum analysis of the colouring-matter
of plants and flowers, some of which were of considerable interest in many
respects. My examinations extended to several hundred different specimens,
from which I was led to conclude that the chromule of flowers is, for the
most part, due to the chemical action of the actinic rays of light over the
protoplasm of the plant, more so than to that of soil. But as certain roots of
plants, as those of the alkanet, yield their colouring-matter to oil, and in a
much smaller degree to spirit or water, it follows then that conclusions of
any kind can only be drawn after a long and careful study of the question.
Some of the results obtained were, however, of some interest at the time,
that, for example, seen in three different solutions of the chlorophyll of
Cinchona succirubra, one of three solutions in alcohol, scarcely coloured,
having in fact only a faint tinge of green colour, and the spectrum of which
much astonished me at the time. It gave four well-marked absorption-bands;
one deep sharp line in the red; another, rather narrower, in the orange,
coincident with D, or the sodium-line; one in the green, about b, coincident
with the Thallium green band; and a fourth on the blue line F, nearly as
broad as that in the red. The ethereal solution gave different results. It
showed only three bands of absorption, nearly the same as in the last case
(though all of them fainter); but the fourth in the blue was not apparent, the
whole of that end of the spectrum being absorbed a little beyond the green
line b. This solution was deep emerald-green, and even dilution did not
alter the phenomena. The acid alcoholic solution was as deeply green as the
last, but gave only the sharp broad absorption-band in the red, and two very
Page 310
faint ghostly bands in the position described above of the D and b lines
respectively.
Further additional researches on the chlorophyll of plants furnished curious
results, the chlorophyll being dissolved out by alcohol, digested for some
hours, and without heat; some plants being fresh, and others dried. Five
classes of phenomena exhibited themselves, but all agreed in having the red
absorption-band broad, sharp, and well defined, some having this one band
only, the Lilac being of this type.
There are two classes in which two absorption-bands occur. One has the red
and the orange bands, of which the Fuchsia, Guelder-rose, and Tansy are
examples; another, in which the red and the green bands are alone co-
existent. Ivy is the type of the class, and it is immaterial whether we take
last year’s leaves or those of the early spring; the results are the same.
The fourth class consists of the two former spectra superposed. Three lines
occur, the red, the orange, and the green bands, at C, D, and b, as before.
This is by far the largest class, and I have thirty or forty examples of it.
Œnothera biennis, Laurestinus, &c., are types with the ethereal solution of
the leaves of Red Bark.
The fifth class consists of those having properties similar to the alcoholic
solution of Red Bark described. But I only found eight of these, and not all
equal in colour power, namely: Berberry, Sloe, Tea, Hyoscyamus, Digitalis,
Senna, and Red Bark. The results obtained appeared at the time to be well
worth following up to a more practical conclusion than that arrived at. It
should be noted that in the preparation of vegetable colouring matters for
the micro-spectroscope, care must be taken to employ only a small quantity
of spirits of wine to filter the solution, and evaporate it at once to dryness at
a very gentle heat, otherwise if we attempt to keep the colouring matters in
a fluid state they quickly decompose. It is necessary also to employ various
re-agents in developing characteristic spectra. The most valuable re-agent is
sulphite of soda. This admits of the division of colours into groups.
It is better to use a dilute alcoholic solution for the extraction of colour from
plants, and to observe the spectrum in a column of about three-quarters of
respectively.
Further additional researches on the chlorophyll of plants furnished curious
results, the chlorophyll being dissolved out by alcohol, digested for some
hours, and without heat; some plants being fresh, and others dried. Five
classes of phenomena exhibited themselves, but all agreed in having the red
absorption-band broad, sharp, and well defined, some having this one band
only, the Lilac being of this type.
There are two classes in which two absorption-bands occur. One has the red
and the orange bands, of which the Fuchsia, Guelder-rose, and Tansy are
examples; another, in which the red and the green bands are alone co-
existent. Ivy is the type of the class, and it is immaterial whether we take
last year’s leaves or those of the early spring; the results are the same.
The fourth class consists of the two former spectra superposed. Three lines
occur, the red, the orange, and the green bands, at C, D, and b, as before.
This is by far the largest class, and I have thirty or forty examples of it.
Œnothera biennis, Laurestinus, &c., are types with the ethereal solution of
the leaves of Red Bark.
The fifth class consists of those having properties similar to the alcoholic
solution of Red Bark described. But I only found eight of these, and not all
equal in colour power, namely: Berberry, Sloe, Tea, Hyoscyamus, Digitalis,
Senna, and Red Bark. The results obtained appeared at the time to be well
worth following up to a more practical conclusion than that arrived at. It
should be noted that in the preparation of vegetable colouring matters for
the micro-spectroscope, care must be taken to employ only a small quantity
of spirits of wine to filter the solution, and evaporate it at once to dryness at
a very gentle heat, otherwise if we attempt to keep the colouring matters in
a fluid state they quickly decompose. It is necessary also to employ various
re-agents in developing characteristic spectra. The most valuable re-agent is
sulphite of soda. This admits of the division of colours into groups.
It is better to use a dilute alcoholic solution for the extraction of colour from
plants, and to observe the spectrum in a column of about three-quarters of
Page 311
an inch in height. By this means it is quite possible to ascertain that the
spectrum of chlorophyll presents seven distinct absorption bands.
For further information on this interesting subject I must refer the reader to
Mr. Sorby’s paper “On a Definite Method of Qualitative Analysis of
Vegetable and Animal Colouring Matter by means of the Spectrum
Microscope,” “Proc. Roy. Soc.,” No. 92, 1867.
spectrum of chlorophyll presents seven distinct absorption bands.
For further information on this interesting subject I must refer the reader to
Mr. Sorby’s paper “On a Definite Method of Qualitative Analysis of
Vegetable and Animal Colouring Matter by means of the Spectrum
Microscope,” “Proc. Roy. Soc.,” No. 92, 1867.
Page 312
CHAPTER IV.
Practical Microscopy: Manipulation, and Mode of Using the
Microscope.
In this chapter it will be my aim to discuss the best practical methods of
employing the microscope and its appliances to the greatest advantage.
First, the student should select a quiet room for working in, with, if
possible, a northern aspect, free from all tremor occasioned by passing
vehicles. The table selected for use should be firm, and provided with
drawers, in which his several appliances can be kept ready to hand. The
microscope must be placed at such an inclination as will enable him to work
in comfort, and without putting strain on the muscles of the neck or
fatiguing the eyes. The next important point is that of light. Daylight, in
some respects, is an advantage; this should come from a white cloud on a
bright day, but as a rule more satisfactory results will be obtained by using a
well-made lamp, as this can be controlled with ease, and used at a proper
height and distance from the microscope. To have a good form of lamp is as
much to be desired for the student as for those engaged in the more
advanced work of microscopy.
Whatever the source of light we must on no account over-illuminate. The
object having been placed on the stage of the microscope, the body should
be racked down to within a quarter or half an inch of the specimen, and
then, while looking through the eye-piece, should be slowly withdrawn
until a sharp image comes into view. The fine adjustment may now be used
for the more delicate focussing of the several parts of the field.
Accurate adjustment of focus is required when using a ¼-inch objective;
details of the object, as striæ, being brought into view when a stronger light
is thrown obliquely upon them from the mirror. If a 1-inch objective is used
Practical Microscopy: Manipulation, and Mode of Using the
Microscope.
In this chapter it will be my aim to discuss the best practical methods of
employing the microscope and its appliances to the greatest advantage.
First, the student should select a quiet room for working in, with, if
possible, a northern aspect, free from all tremor occasioned by passing
vehicles. The table selected for use should be firm, and provided with
drawers, in which his several appliances can be kept ready to hand. The
microscope must be placed at such an inclination as will enable him to work
in comfort, and without putting strain on the muscles of the neck or
fatiguing the eyes. The next important point is that of light. Daylight, in
some respects, is an advantage; this should come from a white cloud on a
bright day, but as a rule more satisfactory results will be obtained by using a
well-made lamp, as this can be controlled with ease, and used at a proper
height and distance from the microscope. To have a good form of lamp is as
much to be desired for the student as for those engaged in the more
advanced work of microscopy.
Whatever the source of light we must on no account over-illuminate. The
object having been placed on the stage of the microscope, the body should
be racked down to within a quarter or half an inch of the specimen, and
then, while looking through the eye-piece, should be slowly withdrawn
until a sharp image comes into view. The fine adjustment may now be used
for the more delicate focussing of the several parts of the field.
Accurate adjustment of focus is required when using a ¼-inch objective;
details of the object, as striæ, being brought into view when a stronger light
is thrown obliquely upon them from the mirror. If a 1-inch objective is used
Page 313
the light often proves to be in excess of what is required, and this must be
regulated by the aid of the diaphragm.
The iris diaphragm, made to drop into the under-stage, is more generally
employed, as when racked up to the object it affords every necessary
graduation of illumination.
To illuminate opaque objects the
light should be thrown upon them
from above by the bull’s-eye lens
(Fig. 201). The focus of such a lens
and the lamp placed at four inches
from it, is about three inches for
daylight, or two inches for artificial
light. A large object may be placed
upon the stage of the microscope at
once, but smaller objects are either
laid on a glass slide or held in the
stage forceps.
When illuminating objects from
above all light from the mirror, or
Fig. 201.—Bull’s-eye Lens.
that which might enter the objective
from below the stage, should be
carefully excluded. Dark-field illumination is a means of seeing a
transparent object as an opaque one. The principle, however, is that all the
light shall be thrown from below the object, but so obliquely that it cannot
enter the object-glass unless interrupted by the object; this is best
accomplished by Wenham’s Parabola.
Glass of any kind requires occasional cleaning; a piece of soft washed
chamois leather should be used for this purpose. The fronts of the objectives
may be carefully wiped, but not unscrewed or tampered with; a short thick-
set camel’s hair brush may be passed down to the back lens, and all dust
removed without doing any harm. If the objective is an immersion, carefully
remove the fluid from the front lens, as even distilled water will leave a
stain behind. For removing oil see special directions given at page 171.
regulated by the aid of the diaphragm.
The iris diaphragm, made to drop into the under-stage, is more generally
employed, as when racked up to the object it affords every necessary
graduation of illumination.
To illuminate opaque objects the
light should be thrown upon them
from above by the bull’s-eye lens
(Fig. 201). The focus of such a lens
and the lamp placed at four inches
from it, is about three inches for
daylight, or two inches for artificial
light. A large object may be placed
upon the stage of the microscope at
once, but smaller objects are either
laid on a glass slide or held in the
stage forceps.
When illuminating objects from
above all light from the mirror, or
Fig. 201.—Bull’s-eye Lens.
that which might enter the objective
from below the stage, should be
carefully excluded. Dark-field illumination is a means of seeing a
transparent object as an opaque one. The principle, however, is that all the
light shall be thrown from below the object, but so obliquely that it cannot
enter the object-glass unless interrupted by the object; this is best
accomplished by Wenham’s Parabola.
Glass of any kind requires occasional cleaning; a piece of soft washed
chamois leather should be used for this purpose. The fronts of the objectives
may be carefully wiped, but not unscrewed or tampered with; a short thick-
set camel’s hair brush may be passed down to the back lens, and all dust
removed without doing any harm. If the objective is an immersion, carefully
remove the fluid from the front lens, as even distilled water will leave a
stain behind. For removing oil see special directions given at page 171.
Page 314
When cleaning the eye-pieces, which should be done occasionally, the cells
containing the glasses must be unscrewed and replaced one at a time, so
that they may not be made to change places.
Any dirt upon the eye-pieces may be detected by turning them round whilst
looking through the instrument; but if the object-glasses are not clean, or
are injured, it will, for the most part, only be seen by the object appearing
misty.
The object-glasses, when in use but not on the microscope, should be stood
upon the table with the screw downwards, to prevent dust getting into the
lenses, and they should always be put into their brass cases when done with.
A large bell-glass shade will be found the most useful cover for keeping
dust from the instrument when not in use.
When looking through the eye-piece be sure to place the eye in close
proximation to the cap, otherwise the whole field will not be perfectly
visible; it should appear as an equally well-illuminated circular disc. If the
eyelashes are reflected from the eye-glass, the observer is looking upon the
eye-piece, and not through it.
The Mirror.—The working focal distance of the mirror is that which brings
the images of the window-bars sharply out upon the object resting upon the
stage. In other words, the focus of the mirror is that which brings parallel
rays to a correct focus on the object-glass. If employing artificial light, then
the flame of the lamp should be distinguishable; a slight change in the
inclination of the mirror will throw the image of the lamp-flame out of the
field.
The strongest light is reflected from the concave side of the mirror, that
from the flat side is more diffuse and less intense. Oblique light can be
obtained by turning the mirror on one side and then adjusting it so as to
illuminate the field from that position. All the necessary mechanism of the
microscope is easily and quickly learned. The object-glasses or objectives
are, as previously explained, designated according to the focal distance of a
single lens of the same magnifying power. Thus a 2-inch objective is
understood to be a combination which has the magnifying power of a single
lens whose focal point is two inches from the object, and so on with
containing the glasses must be unscrewed and replaced one at a time, so
that they may not be made to change places.
Any dirt upon the eye-pieces may be detected by turning them round whilst
looking through the instrument; but if the object-glasses are not clean, or
are injured, it will, for the most part, only be seen by the object appearing
misty.
The object-glasses, when in use but not on the microscope, should be stood
upon the table with the screw downwards, to prevent dust getting into the
lenses, and they should always be put into their brass cases when done with.
A large bell-glass shade will be found the most useful cover for keeping
dust from the instrument when not in use.
When looking through the eye-piece be sure to place the eye in close
proximation to the cap, otherwise the whole field will not be perfectly
visible; it should appear as an equally well-illuminated circular disc. If the
eyelashes are reflected from the eye-glass, the observer is looking upon the
eye-piece, and not through it.
The Mirror.—The working focal distance of the mirror is that which brings
the images of the window-bars sharply out upon the object resting upon the
stage. In other words, the focus of the mirror is that which brings parallel
rays to a correct focus on the object-glass. If employing artificial light, then
the flame of the lamp should be distinguishable; a slight change in the
inclination of the mirror will throw the image of the lamp-flame out of the
field.
The strongest light is reflected from the concave side of the mirror, that
from the flat side is more diffuse and less intense. Oblique light can be
obtained by turning the mirror on one side and then adjusting it so as to
illuminate the field from that position. All the necessary mechanism of the
microscope is easily and quickly learned. The object-glasses or objectives
are, as previously explained, designated according to the focal distance of a
single lens of the same magnifying power. Thus a 2-inch objective is
understood to be a combination which has the magnifying power of a single
lens whose focal point is two inches from the object, and so on with
Page 315
reference to other powers. By the aid of different eye-pieces an extensive
range of magnifying power can be obtained; for example, the 2-inch
objective with a deep eye-piece will give the same amplification as the
quarter objective with the ordinary eye-piece. Indeed, for certain
observations, the combination of a wide-angled low-power objective, with a
deep eye-piece, or compensating eye-piece, is considered to have an
advantage.
It has been already explained that two objectives, one of much greater
power than the other, but both having only the same numerical aperture,
will show only the same amount of detail; the higher power on a larger
scale. That is, supposing with a ¼-inch objective of 1·0 numerical aperture
certain structure is resolved, then a 1⁄8-inch substituted with exactly the same
numerical aperture, but with double the magnification, no more resolving
power will be found in the latter objective than in the former. For this
reason a doubt has been expressed as to whether high-power objectives—
especially the more expensive oil-immersions, made to transmit large
pencils of light through their larger apertures—are so well adapted for
ordinary research as the best series of dry achromatic objectives, or even, in
some instances, the medium aperture lenses; undoubtedly, for histological
(physiological and pathological) work, the latter will be found to meet the
students’ requirements quite as well as the former.
The student or amateur will do well to commence with moderate or medium
powers, a 2-inch, a 1-inch, a ½-inch, a 4⁄10-inch, or ¼-inch. These, together
with the A and B eye-pieces, will give a range of magnification from 30 to
250 diameters.
Penetration in the objective is a quality for consideration, as the adjustment
of high powers is a work of delicacy, and in some cases their penetration is
impaired by the arrangement made to obtain finer definition. The value,
however, of penetration in an objective is always considered to be of more
or less importance. It is a quality whereby, under certain conditions, a more
perfect insight into structure is obtained. As a rule, the objective having the
largest working distance possesses the better penetration. Theoretically, the
penetration of an objective decreases as the square of the angular aperture
increases. For this reason the medical student will be justified in choosing
range of magnifying power can be obtained; for example, the 2-inch
objective with a deep eye-piece will give the same amplification as the
quarter objective with the ordinary eye-piece. Indeed, for certain
observations, the combination of a wide-angled low-power objective, with a
deep eye-piece, or compensating eye-piece, is considered to have an
advantage.
It has been already explained that two objectives, one of much greater
power than the other, but both having only the same numerical aperture,
will show only the same amount of detail; the higher power on a larger
scale. That is, supposing with a ¼-inch objective of 1·0 numerical aperture
certain structure is resolved, then a 1⁄8-inch substituted with exactly the same
numerical aperture, but with double the magnification, no more resolving
power will be found in the latter objective than in the former. For this
reason a doubt has been expressed as to whether high-power objectives—
especially the more expensive oil-immersions, made to transmit large
pencils of light through their larger apertures—are so well adapted for
ordinary research as the best series of dry achromatic objectives, or even, in
some instances, the medium aperture lenses; undoubtedly, for histological
(physiological and pathological) work, the latter will be found to meet the
students’ requirements quite as well as the former.
The student or amateur will do well to commence with moderate or medium
powers, a 2-inch, a 1-inch, a ½-inch, a 4⁄10-inch, or ¼-inch. These, together
with the A and B eye-pieces, will give a range of magnification from 30 to
250 diameters.
Penetration in the objective is a quality for consideration, as the adjustment
of high powers is a work of delicacy, and in some cases their penetration is
impaired by the arrangement made to obtain finer definition. The value,
however, of penetration in an objective is always considered to be of more
or less importance. It is a quality whereby, under certain conditions, a more
perfect insight into structure is obtained. As a rule, the objective having the
largest working distance possesses the better penetration. Theoretically, the
penetration of an objective decreases as the square of the angular aperture
increases. For this reason the medical student will be justified in choosing
Page 316
the objectives I have named, since these will be better adapted to his work
and pursuits. The penetration of the objective is a relative quality assessed
at a different value by workers whose aims are widely different. But for the
observation of living organisms, the cyclosis within the cell of the
closterium or valisneria, for instance, preference will undoubtedly be in
favour of the objective with good penetration.
Resolving Power.—This is a quality highly prized by the bacteriologist. In
the case of the high-angled apochromatic oil-immersion, with its
compensating eye-piece, its resolution is found to be of very considerable
advantage, because of its capacity to receive and recombine all the
diffraction spectra that lie beyond the range of the older achromatic
objective, with its smaller angular aperture. The actual loss of resolving
power consequent upon the contraction of aperture from 180° to 128½° is
ten per cent., if not more. Resolution depends, then, upon the quality and
quantity of the light admitted, the power of collecting the greatest number
of rays, and the perfection of centring. In other words, upon the co-
ordination of the illuminating system of the microscope—mirror,
achromatic condenser, objective and eye-piece. If diatoms are employed as
test-objects, it should not be forgotten that there are great differences, even
in the same species, in the distances their lines are apart. For this reason
ruled lines of known value, as Nobert’s lines, are to be preferred. The
following example will suffice to show the value of a dry 1⁄8-inch objective
of 120° in defining the rulings of a 19-band plate, which is equivalent to the
1⁄67000th of an inch. This objective, with careful illumination, showed them
all; but when cut down by a diaphragm to 110°, the eighteenth line was not
separable; further cut down to 100° the seventeenth was the limit, to 80° the
fourteenth, and to 60° the tenth was barely reached.
Flatness of Field.—This quality in the objective has, by the introduction of
the immersion system, lost much of the importance formerly attached to it.
Some writers assume it to be an “optical impossibility.” The compensating
eye-piece has had the effect of contracting the visual field, consequently the
peripheral imperfections of the objective are of a less disturbing character.
It has, however, not been made perfectly clear whether the highest
perfection of the two primary qualities of a good objective, defining power
and pursuits. The penetration of the objective is a relative quality assessed
at a different value by workers whose aims are widely different. But for the
observation of living organisms, the cyclosis within the cell of the
closterium or valisneria, for instance, preference will undoubtedly be in
favour of the objective with good penetration.
Resolving Power.—This is a quality highly prized by the bacteriologist. In
the case of the high-angled apochromatic oil-immersion, with its
compensating eye-piece, its resolution is found to be of very considerable
advantage, because of its capacity to receive and recombine all the
diffraction spectra that lie beyond the range of the older achromatic
objective, with its smaller angular aperture. The actual loss of resolving
power consequent upon the contraction of aperture from 180° to 128½° is
ten per cent., if not more. Resolution depends, then, upon the quality and
quantity of the light admitted, the power of collecting the greatest number
of rays, and the perfection of centring. In other words, upon the co-
ordination of the illuminating system of the microscope—mirror,
achromatic condenser, objective and eye-piece. If diatoms are employed as
test-objects, it should not be forgotten that there are great differences, even
in the same species, in the distances their lines are apart. For this reason
ruled lines of known value, as Nobert’s lines, are to be preferred. The
following example will suffice to show the value of a dry 1⁄8-inch objective
of 120° in defining the rulings of a 19-band plate, which is equivalent to the
1⁄67000th of an inch. This objective, with careful illumination, showed them
all; but when cut down by a diaphragm to 110°, the eighteenth line was not
separable; further cut down to 100° the seventeenth was the limit, to 80° the
fourteenth, and to 60° the tenth was barely reached.
Flatness of Field.—This quality in the objective has, by the introduction of
the immersion system, lost much of the importance formerly attached to it.
Some writers assume it to be an “optical impossibility.” The compensating
eye-piece has had the effect of contracting the visual field, consequently the
peripheral imperfections of the objective are of a less disturbing character.
It has, however, not been made perfectly clear whether the highest
perfection of the two primary qualities of a good objective, defining power
Page 317
and resolving power, can be always obtained in one and the same
combination of lenses.
Doubtless, defining power can be more satisfactorily determined by the
examination of a suitable object, and the perfection of the image obtained;
to assist in securing which, a solid axial cone of light equal to about three-
fourths of the aperture of the objective must be employed.
To sum up, then, “the focal power of all objectives depends in their perfect
definition, a property on which their converging power depends, and in turn
their magnifying action is dependent; again, focal power is the curvature
imprinted by the lens on a plane wave, and is reciprocal of the true focal
length. It is appropriately expressed in terms of the proper unit of focal
curvature, the dioptric; a unit of curvature.”39
It may be taken as an axiom with
microscopists that “neither the
penetrating power nor the high-
power defining objective is alone
sufficient for every kind of work.
The larger the details of ultimate
structure, the narrower the aperture
—and the converse; the minuter the Fig. 202.—Seiler’s Test Slide.
dimensions of elementary structure,
the wider must be the aperture of the objective.” Every worker with the
microscope must have satisfied himself of the truth of this statement, when
engaged in the study of the movements of living organisms, or defining the
intimate structure of the minuter diatoms, or of the podura scale.
Test for Illumination.—Dr. C. Seiler recommends the human blood
corpuscle as the best test of good illumination. He prepares the object in the
following manner: Take for the purpose a clean glass slide of the ordinary
kind, and place near its extreme edge a drop of fresh blood drawn by
pricking the finger with a needle. Then take another slide of the same size,
with ground edges, and bring one end in contact with the drop of blood, as
shown in Fig. 202, at an angle of 45°; then draw it evenly and quickly
across the underslide, and the result will be to spread out the corpuscles
evenly throughout. Blood discs being lenticular bodies, with depressed
combination of lenses.
Doubtless, defining power can be more satisfactorily determined by the
examination of a suitable object, and the perfection of the image obtained;
to assist in securing which, a solid axial cone of light equal to about three-
fourths of the aperture of the objective must be employed.
To sum up, then, “the focal power of all objectives depends in their perfect
definition, a property on which their converging power depends, and in turn
their magnifying action is dependent; again, focal power is the curvature
imprinted by the lens on a plane wave, and is reciprocal of the true focal
length. It is appropriately expressed in terms of the proper unit of focal
curvature, the dioptric; a unit of curvature.”39
It may be taken as an axiom with
microscopists that “neither the
penetrating power nor the high-
power defining objective is alone
sufficient for every kind of work.
The larger the details of ultimate
structure, the narrower the aperture
—and the converse; the minuter the Fig. 202.—Seiler’s Test Slide.
dimensions of elementary structure,
the wider must be the aperture of the objective.” Every worker with the
microscope must have satisfied himself of the truth of this statement, when
engaged in the study of the movements of living organisms, or defining the
intimate structure of the minuter diatoms, or of the podura scale.
Test for Illumination.—Dr. C. Seiler recommends the human blood
corpuscle as the best test of good illumination. He prepares the object in the
following manner: Take for the purpose a clean glass slide of the ordinary
kind, and place near its extreme edge a drop of fresh blood drawn by
pricking the finger with a needle. Then take another slide of the same size,
with ground edges, and bring one end in contact with the drop of blood, as
shown in Fig. 202, at an angle of 45°; then draw it evenly and quickly
across the underslide, and the result will be to spread out the corpuscles
evenly throughout. Blood discs being lenticular bodies, with depressed
Page 318
centres, act like so many little glass-lenses, and show diffraction rings if the
light is not properly adjusted.40
Errors of Interpretation.—To be in a position to draw an accurate
conclusion of the nature and properties of the object under examination is a
matter of great importance to the microscopist. The viewing of objects by
transmitted light is of quite an exceptional character, rather calculated to
mislead the judgment as well as the eye. It requires, therefore, an unusual
amount of care to avoid falling into errors of interpretation. Among test
objects the precise nature of the structural elements of the Diatomaceæ have
given rise to great divergence of opinion. Then, again, the minute scales of
the podura Springtails, one of the Collembola, and their congeners Lepisma
saccharina, the structure of which is equally debatable. Mr. R. Beck, in an
instructive paper published in the “Transactions of the Royal Microscopical
Society,” says that the scales of the Lepisma can be made to put on an
appearance which bears little resemblance to their actual structure.
Fig. 203.—Portions of Scales of Lepisma.
light is not properly adjusted.40
Errors of Interpretation.—To be in a position to draw an accurate
conclusion of the nature and properties of the object under examination is a
matter of great importance to the microscopist. The viewing of objects by
transmitted light is of quite an exceptional character, rather calculated to
mislead the judgment as well as the eye. It requires, therefore, an unusual
amount of care to avoid falling into errors of interpretation. Among test
objects the precise nature of the structural elements of the Diatomaceæ have
given rise to great divergence of opinion. Then, again, the minute scales of
the podura Springtails, one of the Collembola, and their congeners Lepisma
saccharina, the structure of which is equally debatable. Mr. R. Beck, in an
instructive paper published in the “Transactions of the Royal Microscopical
Society,” says that the scales of the Lepisma can be made to put on an
appearance which bears little resemblance to their actual structure.
Fig. 203.—Portions of Scales of Lepisma.
Page 319
In the more abundant kind of scales the prominent markings appear as a
series of double lines. These run parallel and at considerable intervals from
end to end of the scale, whilst other lines, generally much fainter, radiate
from the quill, and take the same direction as the outline of the scale when
near the fixed or quill end; but there is, in addition, an interrupted
appearance at the sides of the scale, which is very different from the mere
union, or “cross-hatchings,” of the two sets of lines (Fig. 203, Nos. 1 and 2,
the upper portions).
The scales themselves are formed of some truly transparent substance, for
water instantly and almost entirely obliterates their markings, but they
reappear unaltered as the moisture leaves them; therefore the fact of their
being visible at all, under any circumstances, is due to the refraction of light
by superficial irregularities, and the following experiment establishes this
fact, whilst it determines at the same time the structure of each side of the
scale, which it is otherwise impossible to do from the appearance of the
markings in their unaltered state:—
“Remove some of the scales by pressing a clean and dry slide against the
body of the insect, and cover them with a piece of thin glass, which may be
prevented from moving by a little gum at each corner. No. 3 may then be
taken as an exaggerated section of the various parts. A B is the glass slide,
with a scale, C, closely adherent to it, and D the thin glass-cover. If a very
small drop of water be placed at the edge of the thin glass, it will run under
by capillary attraction; but when it reaches the scale, C, it will run first
between it and the glass slide, A B, because the attraction there will be
greater, and consequently the markings on that side of the scale which is in
contact with the slide will be obliterated, while those on the other side will,
for some time at least, remain unaltered: when such is the case, the strongly
marked vertical lines disappear, and the radiating ones become continuous.
(See No. 1, the lower left-hand portion.) To try the same experiment with
the other, or inner surface of the scales, it is only requisite to transfer them,
by pressing the first piece of glass, by which they were taken from the
insect, upon another piece, and then the same process as before may be
repeated with the scales that have adhered to the second slide, the radiating
lines will now disappear, and the vertical ones become continuous. (See No.
2, left portion.) These results, therefore, show that the interrupted
series of double lines. These run parallel and at considerable intervals from
end to end of the scale, whilst other lines, generally much fainter, radiate
from the quill, and take the same direction as the outline of the scale when
near the fixed or quill end; but there is, in addition, an interrupted
appearance at the sides of the scale, which is very different from the mere
union, or “cross-hatchings,” of the two sets of lines (Fig. 203, Nos. 1 and 2,
the upper portions).
The scales themselves are formed of some truly transparent substance, for
water instantly and almost entirely obliterates their markings, but they
reappear unaltered as the moisture leaves them; therefore the fact of their
being visible at all, under any circumstances, is due to the refraction of light
by superficial irregularities, and the following experiment establishes this
fact, whilst it determines at the same time the structure of each side of the
scale, which it is otherwise impossible to do from the appearance of the
markings in their unaltered state:—
“Remove some of the scales by pressing a clean and dry slide against the
body of the insect, and cover them with a piece of thin glass, which may be
prevented from moving by a little gum at each corner. No. 3 may then be
taken as an exaggerated section of the various parts. A B is the glass slide,
with a scale, C, closely adherent to it, and D the thin glass-cover. If a very
small drop of water be placed at the edge of the thin glass, it will run under
by capillary attraction; but when it reaches the scale, C, it will run first
between it and the glass slide, A B, because the attraction there will be
greater, and consequently the markings on that side of the scale which is in
contact with the slide will be obliterated, while those on the other side will,
for some time at least, remain unaltered: when such is the case, the strongly
marked vertical lines disappear, and the radiating ones become continuous.
(See No. 1, the lower left-hand portion.) To try the same experiment with
the other, or inner surface of the scales, it is only requisite to transfer them,
by pressing the first piece of glass, by which they were taken from the
insect, upon another piece, and then the same process as before may be
repeated with the scales that have adhered to the second slide, the radiating
lines will now disappear, and the vertical ones become continuous. (See No.
2, left portion.) These results, therefore, show that the interrupted
Page 320
appearance is produced by two sets of uninterrupted lines on different
surfaces, the lines in each instance being caused by corrugations or folds on
the external surfaces of the scales. Nos. 1 and 2 are parts of a camera lucida
drawing of a scale which happened to have opposite surfaces obliterated in
different parts. No. 4 shows parts of a small scale in a dry and natural state;
at the upper part the interrupted appearance is not much unlike that seen at
the sides of the larger scales; but lower down, where lines of equal strength
cross nearly at right angles, the lines are entirely lost in a series of dots, and
exactly the same appearance is shown in No. 5 to be produced by the two
scales at a part where they overlie each other, although each one separately
shows only parallel vertical lines.”
Fig. 204.—Outer Membrane of Fig. 204a.—Outer Membrane of
Upper Plane of Red Beads Lower Plane of Beads thrown
thrown by each alternate hole from remaining holes of
of grating; on lowering the grating; on raising the focus
focus white interspaces turn white interspaces turn into red
into blue beads. beads.
Objective used, Zeiss’s apochromatic 1⁄12-inch oil-immersion, numerical aperture
1·40, magnifying power 1,750 diameters.
A well-known skilled observer of test objects41 says: “Practically the
resolving power of our achromatic objectives on lined objects reached their
maximum in the late Dr. Woodward’s hands. Amphipleura pellucida was
then, as now, the finest known regular structure of the diatoms. There
appeared then nothing more to be gained in resolution when one of the
apochromatic 1⁄12-inch objectives of Zeiss, with its entire absence of colour,
passed into my hands, and I soon became convinced that it possessed the
surfaces, the lines in each instance being caused by corrugations or folds on
the external surfaces of the scales. Nos. 1 and 2 are parts of a camera lucida
drawing of a scale which happened to have opposite surfaces obliterated in
different parts. No. 4 shows parts of a small scale in a dry and natural state;
at the upper part the interrupted appearance is not much unlike that seen at
the sides of the larger scales; but lower down, where lines of equal strength
cross nearly at right angles, the lines are entirely lost in a series of dots, and
exactly the same appearance is shown in No. 5 to be produced by the two
scales at a part where they overlie each other, although each one separately
shows only parallel vertical lines.”
Fig. 204.—Outer Membrane of Fig. 204a.—Outer Membrane of
Upper Plane of Red Beads Lower Plane of Beads thrown
thrown by each alternate hole from remaining holes of
of grating; on lowering the grating; on raising the focus
focus white interspaces turn white interspaces turn into red
into blue beads. beads.
Objective used, Zeiss’s apochromatic 1⁄12-inch oil-immersion, numerical aperture
1·40, magnifying power 1,750 diameters.
A well-known skilled observer of test objects41 says: “Practically the
resolving power of our achromatic objectives on lined objects reached their
maximum in the late Dr. Woodward’s hands. Amphipleura pellucida was
then, as now, the finest known regular structure of the diatoms. There
appeared then nothing more to be gained in resolution when one of the
apochromatic 1⁄12-inch objectives of Zeiss, with its entire absence of colour,
passed into my hands, and I soon became convinced that it possessed the
Page 321
power of separating the different layers of structure in the valve, beyond the
grasp of the dry-objective. The result of this increase of power enabled me
to split up, as it were, the one plate of silex forming the valve of
Pleurosigma formosum into three layers, and which had never before
appeared to be possible; proving, in fact, that magnification without
corresponding aperture is of little or no account.”
“The intimate structure of these test objects,” says Mr. Smith, “is built up
on one plan, each being composed of two or more layers, (1) a valve with
two layers, as in Pleurosigma balticum; (2) two layers with a grating and
secondary markings placed diagonally, as in Pleurosigma formosum; (3)
with two layers of a net-like structure, as in Pleurosigma angulatum, the
fineness of the striæ or gratings of which measure the 1⁄50000th of an inch.
Five other diatoms afford evidence of this compound structure. The
presence of beads or hemispheres in one of the focal planes, and
depressions or pits in another, are emphasised in the micro-photograph
itself; reduced portions of the valve are represented in Figs. 204 and 204a.”
A portion of a diatom valve, Pleurosigma angulatum, micro-photographed
on a higher scale of magnification, 4,500 diameters, is given further on.
Fig. 205.—Sections of an old-fashioned Glass Tumbler, from photographs
by the late Mr. R. Beck.
grasp of the dry-objective. The result of this increase of power enabled me
to split up, as it were, the one plate of silex forming the valve of
Pleurosigma formosum into three layers, and which had never before
appeared to be possible; proving, in fact, that magnification without
corresponding aperture is of little or no account.”
“The intimate structure of these test objects,” says Mr. Smith, “is built up
on one plan, each being composed of two or more layers, (1) a valve with
two layers, as in Pleurosigma balticum; (2) two layers with a grating and
secondary markings placed diagonally, as in Pleurosigma formosum; (3)
with two layers of a net-like structure, as in Pleurosigma angulatum, the
fineness of the striæ or gratings of which measure the 1⁄50000th of an inch.
Five other diatoms afford evidence of this compound structure. The
presence of beads or hemispheres in one of the focal planes, and
depressions or pits in another, are emphasised in the micro-photograph
itself; reduced portions of the valve are represented in Figs. 204 and 204a.”
A portion of a diatom valve, Pleurosigma angulatum, micro-photographed
on a higher scale of magnification, 4,500 diameters, is given further on.
Fig. 205.—Sections of an old-fashioned Glass Tumbler, from photographs
by the late Mr. R. Beck.
Page 322
Errors of interpretation arise either from the small cones of illumination
afforded by the dry-objective, or the oblique illumination formerly resorted
to for the resolution of these difficult test objects, and several of the lights
and shadows resulting from the refractive power of the object itself. But the
most common error is that produced by the reversal of the lights and
shadows resulting from the refractive powers of the object itself. To make
this clear, I reproduce two reduced photographs of a small section of an old-
fashioned glass tumbler, covered externally with numerous hemispheres,
illuminated by transmitted light (Fig. 205).
This illustration well emphasises the difficulty there is in determining
structure under precisely similar conditions to those we are accustomed to
of examining valves of diatoms under the microscope. If these photographs
be held in front of a strong light, they at once convey different impressions
to the mind, the hemispheres appearing depressions in the one, and raised
beads in the other. Both are prints from the same negative, but in mounting
are reversed; and therefore the apparent dissimilarity is due to a slight
inequality of illumination, which the mind accepts as light and shade.
Very similar appearances to those described will result if a thin plate of
glass were studded with minute, equal, and equi-distant plano-convex
lenses, the foci of which would very nearly lie in the same plane. If the
focal surface, or plane of vision, of the objective be made to coincide with
this plane, a series of bright points will result, from the excess of light
falling on each lens. If the plane of vision be next made to coincide with the
surfaces of the lenses, these points would appear dark, in consequence of
the rays being refracted towards points now out of focus. Lastly, if the plane
of vision be made to coincide with the plane beneath the lenses that contain
their several foci, so that each lens may be, as it were, combined with the
object-glass, then a second series of bright points will result from the
accumulation of the rays transmitted at those points. Moreover, as all rays
capable of entering the objective are concerned in the formation of the
second series of bright focal points, the first series being formed by the rays
of a cone of light only, it is evident that the circle of least confusion must be
much less, and therefore the bright points better defined in the first than in
the last series.
afforded by the dry-objective, or the oblique illumination formerly resorted
to for the resolution of these difficult test objects, and several of the lights
and shadows resulting from the refractive power of the object itself. But the
most common error is that produced by the reversal of the lights and
shadows resulting from the refractive powers of the object itself. To make
this clear, I reproduce two reduced photographs of a small section of an old-
fashioned glass tumbler, covered externally with numerous hemispheres,
illuminated by transmitted light (Fig. 205).
This illustration well emphasises the difficulty there is in determining
structure under precisely similar conditions to those we are accustomed to
of examining valves of diatoms under the microscope. If these photographs
be held in front of a strong light, they at once convey different impressions
to the mind, the hemispheres appearing depressions in the one, and raised
beads in the other. Both are prints from the same negative, but in mounting
are reversed; and therefore the apparent dissimilarity is due to a slight
inequality of illumination, which the mind accepts as light and shade.
Very similar appearances to those described will result if a thin plate of
glass were studded with minute, equal, and equi-distant plano-convex
lenses, the foci of which would very nearly lie in the same plane. If the
focal surface, or plane of vision, of the objective be made to coincide with
this plane, a series of bright points will result, from the excess of light
falling on each lens. If the plane of vision be next made to coincide with the
surfaces of the lenses, these points would appear dark, in consequence of
the rays being refracted towards points now out of focus. Lastly, if the plane
of vision be made to coincide with the plane beneath the lenses that contain
their several foci, so that each lens may be, as it were, combined with the
object-glass, then a second series of bright points will result from the
accumulation of the rays transmitted at those points. Moreover, as all rays
capable of entering the objective are concerned in the formation of the
second series of bright focal points, the first series being formed by the rays
of a cone of light only, it is evident that the circle of least confusion must be
much less, and therefore the bright points better defined in the first than in
the last series.
Page 323
There are no set of objects which have given rise to more discussion as to
their precise character than the scales of the podura (Lepidocyrtus
cervicollis), to the intimate structure of which Mr. Smith turned his
attention, and succeeded, I am inclined to think, in his attempt to settle the
structure of these very minute scales, and which heretofore have been
described as “notes of exclamation.” By the aid of the same power as that
employed in the examination of the pleurosigma formosum, the old
conventional markings have disappeared, and well-defined “featherlets”
have taken their place. By careful focussing up and down, a series of
whitish pin-like bodies is to be seen, with an intervening secondary
structure. A micro-photograph of a portion of a scale taken by Mr. Smith
shows that these pin-like bodies are inserted in a fold of the basement
membrane, which, in his opinion, furnish unmistakable evidence of the fact
that these projecting bodies are real, and must no longer be looked upon as
mere ghosts. Quite recently, a micro-photograph of a portion of a podura
scale was placed in my hands, taken by Mr. J. W. Gifford with a Swift’s 1⁄12-
inch apochromatic objective, of numerical aperture 1·40, and a deep eye-
piece, having a combined magnifying power of 3,827 diameters. Fig. 206
shows a portion of the photograph which, it will be admitted, supports Mr.
Smith’s view of the structure of the podura scale.
their precise character than the scales of the podura (Lepidocyrtus
cervicollis), to the intimate structure of which Mr. Smith turned his
attention, and succeeded, I am inclined to think, in his attempt to settle the
structure of these very minute scales, and which heretofore have been
described as “notes of exclamation.” By the aid of the same power as that
employed in the examination of the pleurosigma formosum, the old
conventional markings have disappeared, and well-defined “featherlets”
have taken their place. By careful focussing up and down, a series of
whitish pin-like bodies is to be seen, with an intervening secondary
structure. A micro-photograph of a portion of a scale taken by Mr. Smith
shows that these pin-like bodies are inserted in a fold of the basement
membrane, which, in his opinion, furnish unmistakable evidence of the fact
that these projecting bodies are real, and must no longer be looked upon as
mere ghosts. Quite recently, a micro-photograph of a portion of a podura
scale was placed in my hands, taken by Mr. J. W. Gifford with a Swift’s 1⁄12-
inch apochromatic objective, of numerical aperture 1·40, and a deep eye-
piece, having a combined magnifying power of 3,827 diameters. Fig. 206
shows a portion of the photograph which, it will be admitted, supports Mr.
Smith’s view of the structure of the podura scale.
Page 324
Fig. 206.—Podura Scale, taken with a 1⁄12 Swift’s Immersion × 3,827.
Many other errors of interpretation are not unknown to the experienced
operator with the microscope, arising, for the most part, from an influence
exerted by peculiarities in the internal structure of certain objects; for
example, that offered by the human hair, and which, when viewed by
transmitted light, presents the appearance of a flattened-out band, with a
darkish centre, due to the refractive influence of the rays of light transmitted
through the hair. That it is a solid or tubular structure is proved by making a
transverse section of the hair-shaft, when it is seen filled up by medullary
matter, the centre being somewhat darker than the outer part. It is, in fact, a
spiral outgrowth of the epithelial scales, overlapping each other, imparting a
striated appearance to the surface. A cylindrical thread of glass in balsam
appears as a flattened, band-like streak, of little brilliancy. Another instance
Many other errors of interpretation are not unknown to the experienced
operator with the microscope, arising, for the most part, from an influence
exerted by peculiarities in the internal structure of certain objects; for
example, that offered by the human hair, and which, when viewed by
transmitted light, presents the appearance of a flattened-out band, with a
darkish centre, due to the refractive influence of the rays of light transmitted
through the hair. That it is a solid or tubular structure is proved by making a
transverse section of the hair-shaft, when it is seen filled up by medullary
matter, the centre being somewhat darker than the outer part. It is, in fact, a
spiral outgrowth of the epithelial scales, overlapping each other, imparting a
striated appearance to the surface. A cylindrical thread of glass in balsam
appears as a flattened, band-like streak, of little brilliancy. Another instance
Page 325
of fallacy arising from diversity in the refractive power of the internal parts
of an object is furnished by the mistakes formerly made with regard to the
true character of the lacunæ and canaliculi of bone structure. These were
long supposed to be solid corpuscles, with radiating opaque filaments
proceeding from a dense centre; on the contrary, they are minute chambers,
with diverging passages—excavations in the solid osseous structure. That
such is the case is shown by the effects of Canada balsam, which infiltrates
the osseous substance.
Air bubbles are a perplexing source of trouble. The better way of becoming
accustomed to deceptive appearances of the kind is to compare the aspect of
globules of oil in water with bubbles of air in water, or Canada balsam.
The molecular movements of finely divided particles, seen in nearly all
cases when certain objects are first suspended in water, or other fluids, are a
frequent cause of embarrassment to beginners. If a minute portion of indigo
or carmine be rubbed up with a little water, and a drop placed on a glass
slide under the microscope, it will at once exhibit a peculiar perpetual
motion appearance. This movement was first observed in the granular
particles seen among pollen grains of plants, known as fovilla, and which
are set free when the pollen is crushed. Important vital endowments were
formerly attributed to these particles, but Dr. Robert Brown showed that
such granules were common enough both in organic and inorganic
substances, and were in no way “indicative of life.”42
Professor Jevons succeeded in throwing light on these curious movements.
He showed that they were not due to evaporation, as some observers
contended, as they continue when all possibility of evaporation is cut off,
when the fluid is surrounded by a layer of oil, and enclosed in an air-tight
case: but as Professor Jevons pointed out, these movements are greatly
affected by the admixture of various substances with water, being increased
by a small quantity of gum, and checked by a drop of sulphuric acid, or a
few grains of some saline substance, which increases the conducting power
of water for electricity. The Brownian movement, now termed pedesis,
much depends upon the size of the particles, their specific gravity, and the
nature of the liquid in which they are immersed.
of an object is furnished by the mistakes formerly made with regard to the
true character of the lacunæ and canaliculi of bone structure. These were
long supposed to be solid corpuscles, with radiating opaque filaments
proceeding from a dense centre; on the contrary, they are minute chambers,
with diverging passages—excavations in the solid osseous structure. That
such is the case is shown by the effects of Canada balsam, which infiltrates
the osseous substance.
Air bubbles are a perplexing source of trouble. The better way of becoming
accustomed to deceptive appearances of the kind is to compare the aspect of
globules of oil in water with bubbles of air in water, or Canada balsam.
The molecular movements of finely divided particles, seen in nearly all
cases when certain objects are first suspended in water, or other fluids, are a
frequent cause of embarrassment to beginners. If a minute portion of indigo
or carmine be rubbed up with a little water, and a drop placed on a glass
slide under the microscope, it will at once exhibit a peculiar perpetual
motion appearance. This movement was first observed in the granular
particles seen among pollen grains of plants, known as fovilla, and which
are set free when the pollen is crushed. Important vital endowments were
formerly attributed to these particles, but Dr. Robert Brown showed that
such granules were common enough both in organic and inorganic
substances, and were in no way “indicative of life.”42
Professor Jevons succeeded in throwing light on these curious movements.
He showed that they were not due to evaporation, as some observers
contended, as they continue when all possibility of evaporation is cut off,
when the fluid is surrounded by a layer of oil, and enclosed in an air-tight
case: but as Professor Jevons pointed out, these movements are greatly
affected by the admixture of various substances with water, being increased
by a small quantity of gum, and checked by a drop of sulphuric acid, or a
few grains of some saline substance, which increases the conducting power
of water for electricity. The Brownian movement, now termed pedesis,
much depends upon the size of the particles, their specific gravity, and the
nature of the liquid in which they are immersed.
Page 326
The correct conclusions to be drawn by the microscopist regarding the
nature of an object will necessarily depend upon previous experience in
microscopic observations, a knowledge of the class of bodies brought under
observation, and the skill of the observer in the use of the instrument—that
is, in securing the best focus possible with any objective brought into use. I
am indebted to Messrs. Beck for the following series of illustrations,
showing the effect of under and over correction of the objective.
Directions for finding the best Focus.
The method of finding and determining when the screw-collar adjustment
of the high-power objective has arrived at a point of perfect definition and
magnification is as follows:—
Select any dark speck of dust, or an opaque portion of the object, and
carefully focus this small particle by working the screw of the fine
adjustment, move the screw up and down until you are satisfied the image
is the sharpest and blackest that can be obtained, then once more test the
focus a little above and a little below while closely scrutinising the effect on
the image. It will now be seen that whereas in focussing on one side of the
best focus the object disappears in a fog, by focussing on the other side it
remains in view for a longer period, but alters its appearance; it is now no
longer a black dot, but a bright dot of light surrounded by a black margin.
The effects being thus dissimilar on different sides of the best focus, show
that the objective is not perfectly adjusted for the cover-glass in use.
The next step is to find out whether the bright image is above or below the
best focus, as on this depends the direction in which the adjustment-collar
should be turned. To determine this it is only necessary to ascertain which
way the slow-motion milled head of the microscope turns when moving the
objective upwards.
In the case under consideration, the bright image will be above the best
focus, which shows that the cover-glass in use is thicker than that for which
the objective is adjusted, consequently the adjustment-collar must be moved
in the opposite direction.
nature of an object will necessarily depend upon previous experience in
microscopic observations, a knowledge of the class of bodies brought under
observation, and the skill of the observer in the use of the instrument—that
is, in securing the best focus possible with any objective brought into use. I
am indebted to Messrs. Beck for the following series of illustrations,
showing the effect of under and over correction of the objective.
Directions for finding the best Focus.
The method of finding and determining when the screw-collar adjustment
of the high-power objective has arrived at a point of perfect definition and
magnification is as follows:—
Select any dark speck of dust, or an opaque portion of the object, and
carefully focus this small particle by working the screw of the fine
adjustment, move the screw up and down until you are satisfied the image
is the sharpest and blackest that can be obtained, then once more test the
focus a little above and a little below while closely scrutinising the effect on
the image. It will now be seen that whereas in focussing on one side of the
best focus the object disappears in a fog, by focussing on the other side it
remains in view for a longer period, but alters its appearance; it is now no
longer a black dot, but a bright dot of light surrounded by a black margin.
The effects being thus dissimilar on different sides of the best focus, show
that the objective is not perfectly adjusted for the cover-glass in use.
The next step is to find out whether the bright image is above or below the
best focus, as on this depends the direction in which the adjustment-collar
should be turned. To determine this it is only necessary to ascertain which
way the slow-motion milled head of the microscope turns when moving the
objective upwards.
In the case under consideration, the bright image will be above the best
focus, which shows that the cover-glass in use is thicker than that for which
the objective is adjusted, consequently the adjustment-collar must be moved
in the opposite direction.
Page 327
Fig. 207.—Podura Scale Test.
If the collar be turned too far in the opposite direction, it will be found that
the bright image is below the best focus, and the cover-glass is then thinner
than that for which the objective is adjusted. The collar must then be turned
back again until the effect on each side of the best focus is exactly similar.
This effect in the case of a circular speck of dust will be that the object
disappears equally rapidly on either side, and does not instantly vanish into
fog, on either side presenting the bright spot appearance, though not in so
marked a degree on either side. When the object is in perfect adjustment the
expansion of the outline is exactly the same, both within and without the
focus.
A different indication, however, is afforded by such test-objects as the finer
diatoms, and the podura scale, in which we have to do with a set of distinct
dots and other markings. If the dots have a tendency to run into lines when
the object is without the focus, the glasses should be brought closer
together; on the contrary, if the lines appear when the object is within the
focal point, the glasses should be farther separated.
If the collar be turned too far in the opposite direction, it will be found that
the bright image is below the best focus, and the cover-glass is then thinner
than that for which the objective is adjusted. The collar must then be turned
back again until the effect on each side of the best focus is exactly similar.
This effect in the case of a circular speck of dust will be that the object
disappears equally rapidly on either side, and does not instantly vanish into
fog, on either side presenting the bright spot appearance, though not in so
marked a degree on either side. When the object is in perfect adjustment the
expansion of the outline is exactly the same, both within and without the
focus.
A different indication, however, is afforded by such test-objects as the finer
diatoms, and the podura scale, in which we have to do with a set of distinct
dots and other markings. If the dots have a tendency to run into lines when
the object is without the focus, the glasses should be brought closer
together; on the contrary, if the lines appear when the object is within the
focal point, the glasses should be farther separated.
Page 328
The adjustment of the objective by the screw-collar in the case of the
podura scale should be carried out in the way described, when the following
effects will be observed to take place, usually in the order of their
arrangement.
Fig. 1 shows the appearance of a podura scale when the adjustment of the
object-glass is correct, and Fig. 2 shows the effect produced on each side of
the exact focus. Fig. 3 shows the way in which the markings individually
divide when all the adjustments are correct, and when the focus is altered
the least possible amount only each way.
Figs. 4 and 5 show the two appearances on one and the other side of the
best focus when the adjustment is incorrect, Fig. 6 showing the appearance
of the same at its best focus.
The scales are magnified 1,300 diameters, and each square measures ·001
of an inch.
This method, however, of finding the best focus of an objective can scarcely
be accomplished without a sub-stage condenser. It may therefore be of
service to the student, and to those who are not disposed to purchase
expensive forms of condensers, to know that either an inch or an inch and a
half objective, or convex-lens mounted on a simple wooden ring with a
flange, can be arranged to slip in the place of the diaphragm under the
stage. This kind of condenser will prove to be of considerable value with a
½-inch, a 4⁄10-inch, and a ¼-inch; while a still more excellent achromatic
condenser can be made out of a Steinheil’s aplanatic-loup arranged to drop
into the central fitting of the sub-stage. As without a condenser of some
kind it is hardly possible to enter upon any course of histological or
scientific research.43
Working Accessories.
Troughs—Live-cages—Compressors.
podura scale should be carried out in the way described, when the following
effects will be observed to take place, usually in the order of their
arrangement.
Fig. 1 shows the appearance of a podura scale when the adjustment of the
object-glass is correct, and Fig. 2 shows the effect produced on each side of
the exact focus. Fig. 3 shows the way in which the markings individually
divide when all the adjustments are correct, and when the focus is altered
the least possible amount only each way.
Figs. 4 and 5 show the two appearances on one and the other side of the
best focus when the adjustment is incorrect, Fig. 6 showing the appearance
of the same at its best focus.
The scales are magnified 1,300 diameters, and each square measures ·001
of an inch.
This method, however, of finding the best focus of an objective can scarcely
be accomplished without a sub-stage condenser. It may therefore be of
service to the student, and to those who are not disposed to purchase
expensive forms of condensers, to know that either an inch or an inch and a
half objective, or convex-lens mounted on a simple wooden ring with a
flange, can be arranged to slip in the place of the diaphragm under the
stage. This kind of condenser will prove to be of considerable value with a
½-inch, a 4⁄10-inch, and a ¼-inch; while a still more excellent achromatic
condenser can be made out of a Steinheil’s aplanatic-loup arranged to drop
into the central fitting of the sub-stage. As without a condenser of some
kind it is hardly possible to enter upon any course of histological or
scientific research.43
Working Accessories.
Troughs—Live-cages—Compressors.
Page 329
A glass plate with a ledge, and some pieces of thin glass, although
applicable for many purposes, are specially designed for objects in fluid.
Thus a drop of fluid containing the object sought for is placed upon the
slide and covered by a piece of thin glass; or, the object being put upon the
glass slide and the thin glass over it, the fluid is applied near one side, and
runs under by capillary attraction.
Fig. 208.—Varley’s Live-box.
Troughs and Live-box.—These are made of various materials, glass,
vulcanite, brass, &c., expressly for examining infusoria and live animals.
They should be so constructed as to admit of the use of a medium power, a
½-inch at least, under the microscope. They should also admit of being
easily cleaned and repaired when broken; matters rarely thought of by those
who construct them. An early devised live-box (Varley’s, Fig. 208) consists
of two circular pieces of brass tubing, one sliding over the other carrying a
disc of glass and fitting over another glass with bevelled edges to prevent
the fluid flowing away.
Fig. 209.—Ross’s Compressorium.
applicable for many purposes, are specially designed for objects in fluid.
Thus a drop of fluid containing the object sought for is placed upon the
slide and covered by a piece of thin glass; or, the object being put upon the
glass slide and the thin glass over it, the fluid is applied near one side, and
runs under by capillary attraction.
Fig. 208.—Varley’s Live-box.
Troughs and Live-box.—These are made of various materials, glass,
vulcanite, brass, &c., expressly for examining infusoria and live animals.
They should be so constructed as to admit of the use of a medium power, a
½-inch at least, under the microscope. They should also admit of being
easily cleaned and repaired when broken; matters rarely thought of by those
who construct them. An early devised live-box (Varley’s, Fig. 208) consists
of two circular pieces of brass tubing, one sliding over the other carrying a
disc of glass and fitting over another glass with bevelled edges to prevent
the fluid flowing away.
Fig. 209.—Ross’s Compressorium.
Page 330
The Compressorium is used for similar purposes. By a graduated pressure
the fluid is thinned out and a higher power can be employed for the
examination of the object. Ross’s early compressorium consists of a plate of
brass about three inches long, having in its centre a circle of glass like the
bottom of the live-box. This piece of glass is set in a frame, B, which slides
in and out so that it can be removed for the convenience of preparing any
object upon it—under water if desirable. The upper movable part, D, is
attached to a screw-motion at C; and at one end of the brass plate, A, which
forms the bed of the instrument, is an upright piece of brass grooved so as
to receive a vertical plate, to which a downward motion is given by a single
fine screw, surrounded by a spiral spring, which elevates the plate as soon
as the screw-pressure is removed.
Fig. 210.—Beck’s Parallel-plate Compressor.
Beck’s Parallel-plate Compressor (Fig. 210) affords a more exact means of
regulating the pressure, and can be used for a variety of purposes. It is also
easily cleaned.
Fig. 211.—Rousselet’s Compressorium.
Rousselet’s Compressorium (Fig. 211) is a very effective form for general
use. It is so arranged that the student has perfect control over the pressure to
the fluid is thinned out and a higher power can be employed for the
examination of the object. Ross’s early compressorium consists of a plate of
brass about three inches long, having in its centre a circle of glass like the
bottom of the live-box. This piece of glass is set in a frame, B, which slides
in and out so that it can be removed for the convenience of preparing any
object upon it—under water if desirable. The upper movable part, D, is
attached to a screw-motion at C; and at one end of the brass plate, A, which
forms the bed of the instrument, is an upright piece of brass grooved so as
to receive a vertical plate, to which a downward motion is given by a single
fine screw, surrounded by a spiral spring, which elevates the plate as soon
as the screw-pressure is removed.
Fig. 210.—Beck’s Parallel-plate Compressor.
Beck’s Parallel-plate Compressor (Fig. 210) affords a more exact means of
regulating the pressure, and can be used for a variety of purposes. It is also
easily cleaned.
Fig. 211.—Rousselet’s Compressorium.
Rousselet’s Compressorium (Fig. 211) is a very effective form for general
use. It is so arranged that the student has perfect control over the pressure to
Page 331
which the specimen should be subjected. The cover-glass is large in
comparison with that beneath; being bevelled causes evaporation to go on
very slowly while the pressure between the two glass surfaces is kept
perfectly parallel.
Botterill’s Live-trough (Fig. 212) consists of two brass plates screwed
together by binding screws, and holding between them two plates of thin
glass, which are maintained at a proper distance by inserting a semicircular
flat disc of india-rubber.
Fig. 212.—Botterill’s Live-trough. Fig. 213.—Glass Trough.
Glass troughs for chara and polypes (a sectional view of one shown at Fig.
213) are made of three pieces of glass, the bottom being a thick strip, and
the front (a) of thinner glass than the back (b); the whole is cemented
together with Jeffery’s marine-glue. The method adopted for confining
objects near the front glass varies according to circumstances. The most
convenient is to place in the trough a piece of glass wide enough to stand
across diagonally, as at c; then, if the object be heavier than water, it will
sink until stopped by the glass plate. At other times, when used to view
chara, the diagonal plate may be made to press it close to the front by
comparison with that beneath; being bevelled causes evaporation to go on
very slowly while the pressure between the two glass surfaces is kept
perfectly parallel.
Botterill’s Live-trough (Fig. 212) consists of two brass plates screwed
together by binding screws, and holding between them two plates of thin
glass, which are maintained at a proper distance by inserting a semicircular
flat disc of india-rubber.
Fig. 212.—Botterill’s Live-trough. Fig. 213.—Glass Trough.
Glass troughs for chara and polypes (a sectional view of one shown at Fig.
213) are made of three pieces of glass, the bottom being a thick strip, and
the front (a) of thinner glass than the back (b); the whole is cemented
together with Jeffery’s marine-glue. The method adopted for confining
objects near the front glass varies according to circumstances. The most
convenient is to place in the trough a piece of glass wide enough to stand
across diagonally, as at c; then, if the object be heavier than water, it will
sink until stopped by the glass plate. At other times, when used to view
chara, the diagonal plate may be made to press it close to the front by
Page 332
means of a wedge of glass or cork. When using the trough the microscope
should be placed in a nearly horizontal position.
Fig. 214.—Weber’s Slip with Convex Cell for use as a Fig. 215.—Current-slide Live-
Live-trough. cell.
Cells for viewing living objects, and watching their movements, take many
forms, usually determined by the makers for the purposes they are required
to serve. The smaller glass troughs (Figs. 216, 216a) are made for
examining the small infusoria, rotifers, &c., some of which take special
forms, as the double or divided trough (Fig. 217) intended for viewing the
circulation of the blood in the tail of a small fish, and at the same time keep
up a supply of water and air.
Fig. 216. Fig. 216a.
The Frog-plate consists of a strip of plate-glass, or wood, pierced with holes
on either side, through which tapes are passed to secure the frog in its place.
At the extreme end is a shallow glass trough, made to hold a sufficient
quantity of water to keep the web of the foot moist while under
examination. In this way a continuous view of the circulation of the blood
of the animal is obtained.
Growing Cells have received more
attention from those who devote attention
to the lower forms of life, the construction
of which, for the purpose of maintaining a
Fig. 217.
continuous supply of fresh water to objects
should be placed in a nearly horizontal position.
Fig. 214.—Weber’s Slip with Convex Cell for use as a Fig. 215.—Current-slide Live-
Live-trough. cell.
Cells for viewing living objects, and watching their movements, take many
forms, usually determined by the makers for the purposes they are required
to serve. The smaller glass troughs (Figs. 216, 216a) are made for
examining the small infusoria, rotifers, &c., some of which take special
forms, as the double or divided trough (Fig. 217) intended for viewing the
circulation of the blood in the tail of a small fish, and at the same time keep
up a supply of water and air.
Fig. 216. Fig. 216a.
The Frog-plate consists of a strip of plate-glass, or wood, pierced with holes
on either side, through which tapes are passed to secure the frog in its place.
At the extreme end is a shallow glass trough, made to hold a sufficient
quantity of water to keep the web of the foot moist while under
examination. In this way a continuous view of the circulation of the blood
of the animal is obtained.
Growing Cells have received more
attention from those who devote attention
to the lower forms of life, the construction
of which, for the purpose of maintaining a
Fig. 217.
continuous supply of fresh water to objects
Page 333
under observation, and for sustaining their vital energy for a long period, is
of some importance. The employment of live-cells is resorted to by
microscopists, as doubtless there is much to be discovered concerning the
metamorphoses which some of the lower micro-organisms, both of plant
and animal life, pass through.
Fig. 218.—Frog-plate.
Holman’s life slide consists of a 3 × 1 inch glass slide, with a deep oval
cavity in the middle to receive the specimen for observation. A shallow oval
is ground and polished around the deep cavity, forming a bevel. From this
bevel a fine cut extends, to furnish fresh air to the living low forms of life
which invariably seek the bevelled edge of the cavity, thus bringing them
within reach of the highest powers. He also contrived a convenient form of
“moist chamber,” or animalcule-cage (Fig. 220), for the purpose of studying
the growth of minute organisms, without in any way disturbing them for a
lengthened period. This is also found useful as a dry chamber for holding
minute insects.
Fig. 219.—Holman’s Life Slide. Full size.
of some importance. The employment of live-cells is resorted to by
microscopists, as doubtless there is much to be discovered concerning the
metamorphoses which some of the lower micro-organisms, both of plant
and animal life, pass through.
Fig. 218.—Frog-plate.
Holman’s life slide consists of a 3 × 1 inch glass slide, with a deep oval
cavity in the middle to receive the specimen for observation. A shallow oval
is ground and polished around the deep cavity, forming a bevel. From this
bevel a fine cut extends, to furnish fresh air to the living low forms of life
which invariably seek the bevelled edge of the cavity, thus bringing them
within reach of the highest powers. He also contrived a convenient form of
“moist chamber,” or animalcule-cage (Fig. 220), for the purpose of studying
the growth of minute organisms, without in any way disturbing them for a
lengthened period. This is also found useful as a dry chamber for holding
minute insects.
Fig. 219.—Holman’s Life Slide. Full size.
Page 334
Fig. 220.—Holman’s Moist Chamber.
Zentmayer’s Holman Syphon Slide is used either as a hot or cold water cell.
It should be deep enough to hold a small fish or newt, and retain it without
any undue pressure. When in use it is only necessary to place the animal
into it (as shown in Fig. 221), with some water, and secure it with a glass
cover; then immerse the upper tube in a jar of water, while another, at a
lower level, maintains a current. When the slide is on the stage of the
microscope, one jar should stand on a lower level than the other, the slide
being made the highest part of the syphon. The pressure of the atmosphere
is sufficient to keep the cover-glass in its place.
The examination of the various kinds of infusorial life—rotifers, for
instance—is facilitated by the addition of the smallest particle of colouring
matter, either carmine or indigo. A small quantity of either of these colours
should be rubbed up in a little water in a watch-glass, and a portion taken
up on the point of a brush, and the brush run along the edge of the cover-
glass; sufficient will be left behind to barely tinge the water with the colour,
and this gradually distributes itself over the rotifers. Under the microscope
this minute quantity will be seen like a rising cloud of dust, and as it
approaches a rotifer it is whirled round in different curves, showing at once
the action of its wonderfully rapid cilia. This colouring matter appears to be
devoured, as it may be traced from the mouth to the digestive canal.
Monads may be detected by this means, and the smaller forms of algæ,
Euglena viridis and Protococcus pluvialis.
Zentmayer’s Holman Syphon Slide is used either as a hot or cold water cell.
It should be deep enough to hold a small fish or newt, and retain it without
any undue pressure. When in use it is only necessary to place the animal
into it (as shown in Fig. 221), with some water, and secure it with a glass
cover; then immerse the upper tube in a jar of water, while another, at a
lower level, maintains a current. When the slide is on the stage of the
microscope, one jar should stand on a lower level than the other, the slide
being made the highest part of the syphon. The pressure of the atmosphere
is sufficient to keep the cover-glass in its place.
The examination of the various kinds of infusorial life—rotifers, for
instance—is facilitated by the addition of the smallest particle of colouring
matter, either carmine or indigo. A small quantity of either of these colours
should be rubbed up in a little water in a watch-glass, and a portion taken
up on the point of a brush, and the brush run along the edge of the cover-
glass; sufficient will be left behind to barely tinge the water with the colour,
and this gradually distributes itself over the rotifers. Under the microscope
this minute quantity will be seen like a rising cloud of dust, and as it
approaches a rotifer it is whirled round in different curves, showing at once
the action of its wonderfully rapid cilia. This colouring matter appears to be
devoured, as it may be traced from the mouth to the digestive canal.
Monads may be detected by this means, and the smaller forms of algæ,
Euglena viridis and Protococcus pluvialis.
Page 335
Fig. 221.—Holman’s Syphon Slide.
Dipping-tubes.—In dealing with infusorial or monad life it is convenient to
keep a stock-bottle ready for their reception, and in a light favourable to
health. When a live specimen is required for examination, the dipping-tube
is brought into requisition. These tubes are open at both ends, and vary in
length and diameter. Their ends should be nicely rounded off in the flame of
a blow-pipe; in form either straight, or bent and drawn out to a fine point, as
represented in Fig. 222. When any special specimen is required for
examination, then one of the tubes must be passed down into the water, the
upper orifice having been previously closed by the forefinger, and kept
tightly pressed, until its lower orifice comes in contact with the object. On
the finger being removed, the water rushes up and carries the creature
sought for with it. The finger is once more replaced at the top of the tube; it
is then lifted out, and the contents deposited in one or other of the glass
cells described. Tubes with india-rubber covers can be had.
Dipping-tubes.—In dealing with infusorial or monad life it is convenient to
keep a stock-bottle ready for their reception, and in a light favourable to
health. When a live specimen is required for examination, the dipping-tube
is brought into requisition. These tubes are open at both ends, and vary in
length and diameter. Their ends should be nicely rounded off in the flame of
a blow-pipe; in form either straight, or bent and drawn out to a fine point, as
represented in Fig. 222. When any special specimen is required for
examination, then one of the tubes must be passed down into the water, the
upper orifice having been previously closed by the forefinger, and kept
tightly pressed, until its lower orifice comes in contact with the object. On
the finger being removed, the water rushes up and carries the creature
sought for with it. The finger is once more replaced at the top of the tube; it
is then lifted out, and the contents deposited in one or other of the glass
cells described. Tubes with india-rubber covers can be had.
Page 336
Fig. 222.—Dipping-tubes. Fig. 223.—Stock-bottle.
Moist and Warm Stages.—In addition to the moist cells and chambers
described it is often found necessary in working out the histories of minute
organisms to keep them for some time under observation, and as far as
possible in an undisturbed condition, and it is equally necessary to prevent
evaporation of the water in which they are immersed. One of the best warm
stages is that known as Maddox’s growing stage; this can be had of any
optician. More elaborate adaptions are required for the study of special
organisms, and for experimental research.
Moist and Warm Stages.—In addition to the moist cells and chambers
described it is often found necessary in working out the histories of minute
organisms to keep them for some time under observation, and as far as
possible in an undisturbed condition, and it is equally necessary to prevent
evaporation of the water in which they are immersed. One of the best warm
stages is that known as Maddox’s growing stage; this can be had of any
optician. More elaborate adaptions are required for the study of special
organisms, and for experimental research.
Page 337
Fig. 224.—Bartley’s Warm Stage.
In that case Bartley’s Warm Stage (Fig. 224) is recommended. There are
other forms of warm stages in use, many of an inexpensive kind and readily
adaptable to any stage. Bartley’s has proved useful; it consists of a vessel,
E, three parts filled with water and supported on a ring stand. This may be
kept at any temperature by the small spirit-lamp, C; a syphon tube d
conveys the warm water along f, and through the bent tubing which
surrounds the object under observation on the stage, D, and then passes off
through the open end, C, into the receptacle, B, placed to receive the
overflow. Steam can be used for heating, or iced water for observing the
effects of cold upon the organism.
A simple form of warm stage may be made of an oblong copper plate, two
inches long by one wide, from one side of which a rod of the same material
projects. The plate has a round aperture, the centre half an inch in diameter,
and is fastened to an ordinary slide with sealing-wax. The drop or object to
be examined is placed on a large-sized cover-glass and covered over with a
smaller one. Olive oil or vaseline is painted round the edge of the smaller
one to prevent evaporation, and the preparation is placed over the aperture
in the plate. The slide bearing the copper plate is clamped to the stage of the
In that case Bartley’s Warm Stage (Fig. 224) is recommended. There are
other forms of warm stages in use, many of an inexpensive kind and readily
adaptable to any stage. Bartley’s has proved useful; it consists of a vessel,
E, three parts filled with water and supported on a ring stand. This may be
kept at any temperature by the small spirit-lamp, C; a syphon tube d
conveys the warm water along f, and through the bent tubing which
surrounds the object under observation on the stage, D, and then passes off
through the open end, C, into the receptacle, B, placed to receive the
overflow. Steam can be used for heating, or iced water for observing the
effects of cold upon the organism.
A simple form of warm stage may be made of an oblong copper plate, two
inches long by one wide, from one side of which a rod of the same material
projects. The plate has a round aperture, the centre half an inch in diameter,
and is fastened to an ordinary slide with sealing-wax. The drop or object to
be examined is placed on a large-sized cover-glass and covered over with a
smaller one. Olive oil or vaseline is painted round the edge of the smaller
one to prevent evaporation, and the preparation is placed over the aperture
in the plate. The slide bearing the copper plate is clamped to the stage of the
Page 338
microscope. The flame of the spirit-lamp is applied to the extremity of the
rod, and the heat is conducted to the plate and thence transmitted to the
specimen. In order that the temperature of the copper plate may be
approximately that of the body, the lamp is so adjusted that a fragment of
cacao butter and wax placed close to the preparation is melted.
Professors Stricker and Schäfer have constructed warm stages for accurate
observations, and which fully answer every purpose.
Fig. 225.—Stricker’s Warm Stage.
Stricker’s Stage (Fig. 225) consists of a rectangular box with a central
opening, C, permitting the passage of light through the specimen under
examination. The water makes its exit and entrance at the side tubes B B′,
and the temperature is indicated by a thermometer in front. In this apparatus
either warm or cold water can be continuously used.
rod, and the heat is conducted to the plate and thence transmitted to the
specimen. In order that the temperature of the copper plate may be
approximately that of the body, the lamp is so adjusted that a fragment of
cacao butter and wax placed close to the preparation is melted.
Professors Stricker and Schäfer have constructed warm stages for accurate
observations, and which fully answer every purpose.
Fig. 225.—Stricker’s Warm Stage.
Stricker’s Stage (Fig. 225) consists of a rectangular box with a central
opening, C, permitting the passage of light through the specimen under
examination. The water makes its exit and entrance at the side tubes B B′,
and the temperature is indicated by a thermometer in front. In this apparatus
either warm or cold water can be continuously used.
Page 339
Fig. 226.—Schäfer’s Warm Stage.
Schäfer’s apparatus (Fig. 226) consists of a vessel filled with water (seen
near the stage) which has been first boiled to expel the air, and then heated
by means of a gas flame. The warm water ascends the india-rubber tubing
to the brass box on the stage. The box is pierced by a tubular aperture to
admit light to the object, and has an exit tube by which the cooled water
from the stage returns by another piece of tubing to be reheated by the gas
flame. There is a gas-regulator, by means of which any temperature can be
maintained.
Methods of Preparing, Hardening, Staining and Section Cutting.
Numerous methods are employed for the preparation, hardening, staining,
and section cutting of animal and vegetable tissues for the microscope, the
details of which are modified, or varied as may be found needful, from time
to time, by those whose intimate acquaintance with the subject entitles them
to make innovations and changes in this very important department of
microscopy. In the hands of the original worker, formulæ and methods will
only be regarded as finger-posts pointing out a means of saving time in
turning over pages to find this or that special method of staining. For this
particular reason I have collected all the most accredited formulæ together
in an Appendix at the end of the book, and arranged them alphabetically for
ready reference.
As to section cutting, the student will do well to practise himself in making
dissections, thick and thin sections, of vegetable and animal substances. The
medical student will require no advice on this point, as the use of the
scalpel, and those instruments needed for microscopical work, form an
important part of his education. Of all the instruments contrived for delicate
dissections, none are more serviceable than those which the student may
make for himself out of ordinary needles. These may be fixed in handles as
represented in Fig. 229, in addition to which, a pair of scissors and forceps,
and a few small knives, such as those used in eye-operations, will prove
most suitable. The double-bladed scissors represented in Fig. 227, with
Schäfer’s apparatus (Fig. 226) consists of a vessel filled with water (seen
near the stage) which has been first boiled to expel the air, and then heated
by means of a gas flame. The warm water ascends the india-rubber tubing
to the brass box on the stage. The box is pierced by a tubular aperture to
admit light to the object, and has an exit tube by which the cooled water
from the stage returns by another piece of tubing to be reheated by the gas
flame. There is a gas-regulator, by means of which any temperature can be
maintained.
Methods of Preparing, Hardening, Staining and Section Cutting.
Numerous methods are employed for the preparation, hardening, staining,
and section cutting of animal and vegetable tissues for the microscope, the
details of which are modified, or varied as may be found needful, from time
to time, by those whose intimate acquaintance with the subject entitles them
to make innovations and changes in this very important department of
microscopy. In the hands of the original worker, formulæ and methods will
only be regarded as finger-posts pointing out a means of saving time in
turning over pages to find this or that special method of staining. For this
particular reason I have collected all the most accredited formulæ together
in an Appendix at the end of the book, and arranged them alphabetically for
ready reference.
As to section cutting, the student will do well to practise himself in making
dissections, thick and thin sections, of vegetable and animal substances. The
medical student will require no advice on this point, as the use of the
scalpel, and those instruments needed for microscopical work, form an
important part of his education. Of all the instruments contrived for delicate
dissections, none are more serviceable than those which the student may
make for himself out of ordinary needles. These may be fixed in handles as
represented in Fig. 229, in addition to which, a pair of scissors and forceps,
and a few small knives, such as those used in eye-operations, will prove
most suitable. The double-bladed scissors represented in Fig. 227, with
Page 340
curved blades, are brought into use for cutting vegetable and other soft
structures, the disadvantage attendant upon the use of which is owing to the
curvature of the blades; when dealing with flat surfaces, the middle of the
section is left too thick to exhibit structure.
The double-bladed knife of Professor Valentin was formerly held in high
estimation by the microscopist, but this has been almost superseded by the
microtome, which has taken the place of all other instruments, since by its
aid uniform series of nearly all substances can be cut. The standard unit of a
perfect section cutter, of any kind, has been fixed by the Royal
Microscopical Society at the one-thousandth of a millimetre.
Fig. 227.—Section Scissors and Forceps.
The use of the razor for cutting sections has not been wholly abandoned, the
method of using which is as follows:—Take the tissue between the thumb
and finger of the left hand, hold the finger horizontally, so that its upper
surface may form a rest for the razor to glide upon, take the razor firmly,
and keep the handle in a line with the blade, then draw it through the tissue
from heel to point and towards yourself. While cutting keep the razor well
wetted with diluted methylated spirit.
structures, the disadvantage attendant upon the use of which is owing to the
curvature of the blades; when dealing with flat surfaces, the middle of the
section is left too thick to exhibit structure.
The double-bladed knife of Professor Valentin was formerly held in high
estimation by the microscopist, but this has been almost superseded by the
microtome, which has taken the place of all other instruments, since by its
aid uniform series of nearly all substances can be cut. The standard unit of a
perfect section cutter, of any kind, has been fixed by the Royal
Microscopical Society at the one-thousandth of a millimetre.
Fig. 227.—Section Scissors and Forceps.
The use of the razor for cutting sections has not been wholly abandoned, the
method of using which is as follows:—Take the tissue between the thumb
and finger of the left hand, hold the finger horizontally, so that its upper
surface may form a rest for the razor to glide upon, take the razor firmly,
and keep the handle in a line with the blade, then draw it through the tissue
from heel to point and towards yourself. While cutting keep the razor well
wetted with diluted methylated spirit.
Page 341
Fig. 228.—Dissecting Knives.
Some preparation is required for cutting sections with the single microtome.
The substance to be cut must be embedded in some other material, as carrot,
turnip, potato, alder pith, paraffin, or thick gum, with either of which the
cylinder or well of the microtome must be so nearly filled as to leave only
an excavation in the centre for the specimen to be operated upon to occupy.
The various forms of microtomes in use, and the selection of the most
suitable, is therefore a matter of some difficulty. I must content myself by
particularising two or three typical forms in general use. As all the
substances intended for cutting require preparation, it will be first necessary
to attend to the following directions given by one experienced in section
cutting, Mr. M. J. Cole44:—(1) Always use fresh tissues. (2) Cut the organs
into small pieces with a sharp knife. (3) Never wash a specimen in water;
when it is necessary to remove any matter, allow some weak salt solution to
flow over the surface of the tissue, or wash it in some hardening re-agent.
(4) All specimens should be hardened in a large quantity of the re-agent; too
many pieces should not be put into the same bottle, and keep them in a cool
place. (5) In all cases the hardening process must be completed in spirits.
(6) Label the bottles, stating the contents, the hardening fluid used, and
when changed. Attention to details is necessary, as if hardening is
neglected, good sections cannot be made.
Embedding in Paraffin Wax or Lard.—Melt together, by the aid of gentle
heat, four parts of solid paraffin and one part of lard. A quantity of this may
be made and kept ready for use. Melt the paraffin mass over a water bath,
take the specimen, and dry it between the folds of a cloth to remove the
spirit, so that the paraffin may adhere to its surface, place it in a small chip-
box, in the desired position, and pour in enough melted paraffin to cover it,
then set aside to solidify; when quite cold break away the box, and cut
sections from the embedded mass with a sharp razor.
Some preparation is required for cutting sections with the single microtome.
The substance to be cut must be embedded in some other material, as carrot,
turnip, potato, alder pith, paraffin, or thick gum, with either of which the
cylinder or well of the microtome must be so nearly filled as to leave only
an excavation in the centre for the specimen to be operated upon to occupy.
The various forms of microtomes in use, and the selection of the most
suitable, is therefore a matter of some difficulty. I must content myself by
particularising two or three typical forms in general use. As all the
substances intended for cutting require preparation, it will be first necessary
to attend to the following directions given by one experienced in section
cutting, Mr. M. J. Cole44:—(1) Always use fresh tissues. (2) Cut the organs
into small pieces with a sharp knife. (3) Never wash a specimen in water;
when it is necessary to remove any matter, allow some weak salt solution to
flow over the surface of the tissue, or wash it in some hardening re-agent.
(4) All specimens should be hardened in a large quantity of the re-agent; too
many pieces should not be put into the same bottle, and keep them in a cool
place. (5) In all cases the hardening process must be completed in spirits.
(6) Label the bottles, stating the contents, the hardening fluid used, and
when changed. Attention to details is necessary, as if hardening is
neglected, good sections cannot be made.
Embedding in Paraffin Wax or Lard.—Melt together, by the aid of gentle
heat, four parts of solid paraffin and one part of lard. A quantity of this may
be made and kept ready for use. Melt the paraffin mass over a water bath,
take the specimen, and dry it between the folds of a cloth to remove the
spirit, so that the paraffin may adhere to its surface, place it in a small chip-
box, in the desired position, and pour in enough melted paraffin to cover it,
then set aside to solidify; when quite cold break away the box, and cut
sections from the embedded mass with a sharp razor.
Page 342
To infiltrate a tissue with paraffin, place the specimen in absolute alcohol or
chloroform for an hour or two, then transfer to a bath of melted paraffin, at
its melting point (about 110° F.), and keep it at this temperature for several
hours, so that the paraffin may penetrate to the middle of the tissue. Then
remove the specimen from the paraffin and put it into a small chip-box,
pour in enough paraffin to cover it, and set aside to cool. When quite cold,
make sections as before, with a razor, or fix it into a microtome, with a little
melted paraffin. The sections when cut must be placed in turpentine to
remove the paraffin, and then into absolute alcohol to remove the
turpentine, and finally in distilled water to remove the alcohol, when they
may be forthwith stained. It is often found better to stain the tissue in bulk
before embedding. In this case the sections will only require the turpentine
to dissolve away the paraffin, and may then be mounted in Canada balsam.
Hardening and Preparing Animal Tissues for section cutting and
microscopical examination.—Fresh tissues are not well suited for
microscopical examination, but it is sometimes advisable to observe the
appearances of a fresh specimen, especially if it is suspected to contain
amaloid bodies or parasites. It will then be necessary to tease out a small
portion of the tissue immersed in a weak solution of salt and water by the
aid of a pair of fine needles (Fig. 229) and the dissecting microscope (Fig.
230).
Fig. 229.—Needles for teasing out Sections.
chloroform for an hour or two, then transfer to a bath of melted paraffin, at
its melting point (about 110° F.), and keep it at this temperature for several
hours, so that the paraffin may penetrate to the middle of the tissue. Then
remove the specimen from the paraffin and put it into a small chip-box,
pour in enough paraffin to cover it, and set aside to cool. When quite cold,
make sections as before, with a razor, or fix it into a microtome, with a little
melted paraffin. The sections when cut must be placed in turpentine to
remove the paraffin, and then into absolute alcohol to remove the
turpentine, and finally in distilled water to remove the alcohol, when they
may be forthwith stained. It is often found better to stain the tissue in bulk
before embedding. In this case the sections will only require the turpentine
to dissolve away the paraffin, and may then be mounted in Canada balsam.
Hardening and Preparing Animal Tissues for section cutting and
microscopical examination.—Fresh tissues are not well suited for
microscopical examination, but it is sometimes advisable to observe the
appearances of a fresh specimen, especially if it is suspected to contain
amaloid bodies or parasites. It will then be necessary to tease out a small
portion of the tissue immersed in a weak solution of salt and water by the
aid of a pair of fine needles (Fig. 229) and the dissecting microscope (Fig.
230).
Fig. 229.—Needles for teasing out Sections.
Page 343
Fig. 230.—Dissecting Microscope.
The most important point in connection with an instrument of this kind is,
that it affords firm and convenient rests for the hands, and should not be
raised too high from the table.
The stage should either be made of glass, or provided with a glass dish for
dissecting under water, or preservative fluid. A pair of aplanatic lenses,
mounted on a focussing bar as shown in Fig. 230, will be found the most
convenient to work with.
Investigations of this nature should be always carried out in the manner
described, but preparations of the kind cannot be preserved any length of
time, unless properly hardened in spirit or Formalin solution. The method of
teasing out under the light of a condensing lens is shown in Fig. 231.
The most important point in connection with an instrument of this kind is,
that it affords firm and convenient rests for the hands, and should not be
raised too high from the table.
The stage should either be made of glass, or provided with a glass dish for
dissecting under water, or preservative fluid. A pair of aplanatic lenses,
mounted on a focussing bar as shown in Fig. 230, will be found the most
convenient to work with.
Investigations of this nature should be always carried out in the manner
described, but preparations of the kind cannot be preserved any length of
time, unless properly hardened in spirit or Formalin solution. The method of
teasing out under the light of a condensing lens is shown in Fig. 231.
Page 344
Fig. 231.—Method of teasing out Muscular Fibre, &c., in a fluid medium under
Condensed Light.
It may be as well to state at the outset that physiological and pathological
tissues can be hardened by immersion in methylated spirit alone, or a
saturated solution of picric acid in methylated spirit in about a week, and it
is said to yield satisfactory results, even some of the tissues being ready in
twenty-four hours. The only drawback is that sections thus quickly
hardened must be stained with picro-carmine. But, whatever method of
hardening adopted, the tissue should be washed by means of a stream of
water for half an hour, to remove all traces of the hardening agent, and on
its removal pressed between folds of cotton cloth or fine Swedish filtering
paper.
The principal hardening re-agents usually kept in bulk ready for use are the
following:—
Absolute Alcohol.—This is suitable for the internal organs of animals,
glands, &c. These organs must be perfectly fresh, and should be cut into
Condensed Light.
It may be as well to state at the outset that physiological and pathological
tissues can be hardened by immersion in methylated spirit alone, or a
saturated solution of picric acid in methylated spirit in about a week, and it
is said to yield satisfactory results, even some of the tissues being ready in
twenty-four hours. The only drawback is that sections thus quickly
hardened must be stained with picro-carmine. But, whatever method of
hardening adopted, the tissue should be washed by means of a stream of
water for half an hour, to remove all traces of the hardening agent, and on
its removal pressed between folds of cotton cloth or fine Swedish filtering
paper.
The principal hardening re-agents usually kept in bulk ready for use are the
following:—
Absolute Alcohol.—This is suitable for the internal organs of animals,
glands, &c. These organs must be perfectly fresh, and should be cut into
Page 345
small pieces, so that the alcohol may penetrate them as quickly as possible.
The hardening is usually complete in a short time.45
Chromic Acid and Spirit.—Chromic acid one-sixth per cent., water solution
two parts, and methylated spirit one part. This reagent hardens in about ten
days. Then transfer to methylated spirit, which should be changed every day
until all colour is discharged from the tissue. This is a suitable reagent for
the preparation of cartilage, nerve trunks, heart, lips, blood vessels, trachea,
lungs, tongue, intestines, and gullet.
Potassium Bichromate.—-Make a two per cent. water solution of this salt.
This will harden specimens in about three weeks. Then transfer the
preparation to methylated spirit, and change it every day until all colour is
discharged. This is suitable for spinal cord, medulla, cerebellum, and
cerebrum.
Müller’s Fluid.—Bichromate of potash 30 grains, sulphate of soda 15
grains, distilled water 3½ ounces. This hardens in from three to six weeks.
Then transfer, as before, to methylated spirits, and change it every day until
colour ceases to appear. Most suitable for lymphatic glands, eye-ball and its
internal structures, as well as for tendons, and thymus gland.
Methylated Spirit may be generally employed, but it has a tendency to
shrink some tissues too much; it hardens in about ten days. It is usual to
change the spirit daily, for the first three days at least. Skin, mammary
gland, supra-renal glands, tonsils, and all injected organs may be hardened
in it. (See note on the adulteration of methylated spirit with rack-oil, which
utterly spoils it for use.)
Decalcifying solution for bones and teeth. Take one-sixth per cent. watery
solution of chromic acid, and to every measured ounce add five drops of
nitric acid. This reagent will soften the femur of any small animal in about
three weeks; larger require a longer time. Change the fluid several times,
and test its action by running a needle through the thickest part of the bone.
Should it not pass through easily, then continue the process until it does.
When soft enough transfer to water, let it soak for an hour or two, then pour
off the water and add ten per cent. solution of carbonate of soda, and soak
for twelve hours to remove all trace of acid. Wash again in water, and
The hardening is usually complete in a short time.45
Chromic Acid and Spirit.—Chromic acid one-sixth per cent., water solution
two parts, and methylated spirit one part. This reagent hardens in about ten
days. Then transfer to methylated spirit, which should be changed every day
until all colour is discharged from the tissue. This is a suitable reagent for
the preparation of cartilage, nerve trunks, heart, lips, blood vessels, trachea,
lungs, tongue, intestines, and gullet.
Potassium Bichromate.—-Make a two per cent. water solution of this salt.
This will harden specimens in about three weeks. Then transfer the
preparation to methylated spirit, and change it every day until all colour is
discharged. This is suitable for spinal cord, medulla, cerebellum, and
cerebrum.
Müller’s Fluid.—Bichromate of potash 30 grains, sulphate of soda 15
grains, distilled water 3½ ounces. This hardens in from three to six weeks.
Then transfer, as before, to methylated spirits, and change it every day until
colour ceases to appear. Most suitable for lymphatic glands, eye-ball and its
internal structures, as well as for tendons, and thymus gland.
Methylated Spirit may be generally employed, but it has a tendency to
shrink some tissues too much; it hardens in about ten days. It is usual to
change the spirit daily, for the first three days at least. Skin, mammary
gland, supra-renal glands, tonsils, and all injected organs may be hardened
in it. (See note on the adulteration of methylated spirit with rack-oil, which
utterly spoils it for use.)
Decalcifying solution for bones and teeth. Take one-sixth per cent. watery
solution of chromic acid, and to every measured ounce add five drops of
nitric acid. This reagent will soften the femur of any small animal in about
three weeks; larger require a longer time. Change the fluid several times,
and test its action by running a needle through the thickest part of the bone.
Should it not pass through easily, then continue the process until it does.
When soft enough transfer to water, let it soak for an hour or two, then pour
off the water and add ten per cent. solution of carbonate of soda, and soak
for twelve hours to remove all trace of acid. Wash again in water, and
Page 346
transfer to methylated spirit until required. Teeth require a large quantity of
the decalcifying solution for softening.
Microtomes.—The simplest form of “hand-cutting machine” is that worked
by a screw, which raises the preparation, and at the same time regulates the
fineness of the section. When a number of sections are required, or when a
complete series of sections of an organ is desired, Cole’s simple microtome
(Fig. 233) is in every way adapted.
Fig. 232.—Hand Section
Cutter. Fig. 233.—Cole’s Section Cutting Microtome.
The method of using it is as follows:—Screw the microtome firmly to the
table, and with the brass tube supplied with the microtome, punch out a
cylinder of carrot to fit into the well. Cut this in half longitudinally, and
scrape out enough space in one half of the carrot to take the specimen; then
place the other half of carrot in position, and make sure that the specimen is
held firmly between them, but it must not be crushed. Now put the cylinder
of carrot and specimen into the well of the microtome and commence
cutting the section. A good razor will do, but it is better to use the knife
which Messrs. Watson supply with the microtome. While cutting keep the
knife and plate of the microtome well wetted with dilute methylated spirit,
and as sections are cut place them in a saucer of dilute spirit. A number of
the decalcifying solution for softening.
Microtomes.—The simplest form of “hand-cutting machine” is that worked
by a screw, which raises the preparation, and at the same time regulates the
fineness of the section. When a number of sections are required, or when a
complete series of sections of an organ is desired, Cole’s simple microtome
(Fig. 233) is in every way adapted.
Fig. 232.—Hand Section
Cutter. Fig. 233.—Cole’s Section Cutting Microtome.
The method of using it is as follows:—Screw the microtome firmly to the
table, and with the brass tube supplied with the microtome, punch out a
cylinder of carrot to fit into the well. Cut this in half longitudinally, and
scrape out enough space in one half of the carrot to take the specimen; then
place the other half of carrot in position, and make sure that the specimen is
held firmly between them, but it must not be crushed. Now put the cylinder
of carrot and specimen into the well of the microtome and commence
cutting the section. A good razor will do, but it is better to use the knife
which Messrs. Watson supply with the microtome. While cutting keep the
knife and plate of the microtome well wetted with dilute methylated spirit,
and as sections are cut place them in a saucer of dilute spirit. A number of
Page 347
sections may be cut and preserved in methylated spirit until required for
examination or mounting.
When a specimen has a very irregular outline, it cannot be very successfully
embedded in carrot; paraffin will then be found to be more suitable. Place
the tissue in the well of the microtome in the proper position, pour in
enough melted paraffin to cover it, and put it by to get cold and hard before
attempting to cut sections.
Fig. 234.—The Cambridge Rocking Microtome.
Cambridge Rocking Microtome.—This new pattern Cambridge Rocking
Microtome (Fig. 234) possesses advantages over other instruments in use
for cutting flat sections, and not parts of a cylindrical surface. The tube
containing the paraffin is 30 millimetres in internal diameter instead of 20
millimetres, as in the earlier forms. The forward movement is also
increased, so that an object 12 millimetres long can be cut throughout its
whole length. It is provided with a dividing arc for reading off the thickness
of the section in thousandths of a millimetre. The razor may be fixed either
with its edge at right angles to the direction of motion of the object, or
diagonally, for giving a slicing cut. The object can also be raised and fixed
in position clear of the razor.
This microtome has both steadiness and stiffness in its geometrical
arrangement and bearings, while the simplicity and efficiency of its
examination or mounting.
When a specimen has a very irregular outline, it cannot be very successfully
embedded in carrot; paraffin will then be found to be more suitable. Place
the tissue in the well of the microtome in the proper position, pour in
enough melted paraffin to cover it, and put it by to get cold and hard before
attempting to cut sections.
Fig. 234.—The Cambridge Rocking Microtome.
Cambridge Rocking Microtome.—This new pattern Cambridge Rocking
Microtome (Fig. 234) possesses advantages over other instruments in use
for cutting flat sections, and not parts of a cylindrical surface. The tube
containing the paraffin is 30 millimetres in internal diameter instead of 20
millimetres, as in the earlier forms. The forward movement is also
increased, so that an object 12 millimetres long can be cut throughout its
whole length. It is provided with a dividing arc for reading off the thickness
of the section in thousandths of a millimetre. The razor may be fixed either
with its edge at right angles to the direction of motion of the object, or
diagonally, for giving a slicing cut. The object can also be raised and fixed
in position clear of the razor.
This microtome has both steadiness and stiffness in its geometrical
arrangement and bearings, while the simplicity and efficiency of its
Page 348
mechanism for advancing the section between each stroke of the razor is
remarkable. Although it may appear more complicated at first sight, it is
found not to be so when brought into use.
Fig. 235a.—Section Cutting Holder
Fig. 235.—Cathcart’s Microtome. for Microtome.
Cathcart’s Freezing Microtome.—This is a convenient and useful
microtome for freezing purposes. Since its first introduction it has been
much improved. The clamping arrangements give steadiness, and the
principal screw is more effective; the freezing-plate is circular, and the
arrangements made for preventing the ether from reaching the upper plate
secures the object in view. This instrument can now be used for embedding
as well as freezing. The directions for freezing are as follows:—
1. Place a few drops of mucilage (one part gum to three parts water) on the
zinc plate.
2. Take a piece of the tissue to be cut, of about a quarter of an inch in
thickness, and press it into the gum.
3. Fill the ether bottle with anhydrous methylated ether, and push the spray
points into their socket. All spirit must of course have been previously
removed by soaking for a night in water. The tissue should afterwards be
soaked in gum for a like time before being cut.
Work the spray bellows briskly until the gum begins to freeze; after this
work more gently. Be always careful to brush off the frozen vapour which,
remarkable. Although it may appear more complicated at first sight, it is
found not to be so when brought into use.
Fig. 235a.—Section Cutting Holder
Fig. 235.—Cathcart’s Microtome. for Microtome.
Cathcart’s Freezing Microtome.—This is a convenient and useful
microtome for freezing purposes. Since its first introduction it has been
much improved. The clamping arrangements give steadiness, and the
principal screw is more effective; the freezing-plate is circular, and the
arrangements made for preventing the ether from reaching the upper plate
secures the object in view. This instrument can now be used for embedding
as well as freezing. The directions for freezing are as follows:—
1. Place a few drops of mucilage (one part gum to three parts water) on the
zinc plate.
2. Take a piece of the tissue to be cut, of about a quarter of an inch in
thickness, and press it into the gum.
3. Fill the ether bottle with anhydrous methylated ether, and push the spray
points into their socket. All spirit must of course have been previously
removed by soaking for a night in water. The tissue should afterwards be
soaked in gum for a like time before being cut.
Work the spray bellows briskly until the gum begins to freeze; after this
work more gently. Be always careful to brush off the frozen vapour which,
Page 349
in a moist atmosphere, may collect below the zinc plate. If the ether should
tend to collect in drops below the plate, work the bellows slower.
5. Raise the tissue by turning the milled head, and cut by sliding the knife
along the glass plates.
6. After use, be careful to wipe the whole instrument clean.
7. Should the ether point become choked, clear by means of the fine wire
provided for the purpose.
8. The instrument is intended for use with methylated sulphuric ether.
9. In clamping the instrument to a table, or other support, care should be
taken that the zinc plate is in a horizontal position. If the plate be not
horizontal, the gum will tend to run to one side.
The arrangement made for cutting and embedding sections consists of a
cylindrical tube (Fig. 235a) fitting into the principal well of the microtome,
within which is a hinged plate, upon which the screw acts, as in an ordinary
vice. To bring this into use the freezing apparatus must be first removed,
and the embedding tube placed in the well, and firmly pressed into place.
Staining Animal Structures.
Specific stains are chiefly employed to assist the eye in distinguishing one
elementary tissue from another. It is therefore necessary to stain all
structures, as certain parts are seen to have a special affinity for one
colouring agent rather than another, whereby they become more deeply
stained, and consequently more clearly differentiated. For staining animal
structures, borax, carmine, and hæmatoxylin are more frequently employed
than others. The formulæ for each will be found in the Appendix “Formulæ
and Methods.”
Staining Process.—Place the section in distilled water to wash away the
alcohol; place a little of the carmine in a watch glass, and immerse the
section in it for four or five minutes; then remove it to a solution composed
tend to collect in drops below the plate, work the bellows slower.
5. Raise the tissue by turning the milled head, and cut by sliding the knife
along the glass plates.
6. After use, be careful to wipe the whole instrument clean.
7. Should the ether point become choked, clear by means of the fine wire
provided for the purpose.
8. The instrument is intended for use with methylated sulphuric ether.
9. In clamping the instrument to a table, or other support, care should be
taken that the zinc plate is in a horizontal position. If the plate be not
horizontal, the gum will tend to run to one side.
The arrangement made for cutting and embedding sections consists of a
cylindrical tube (Fig. 235a) fitting into the principal well of the microtome,
within which is a hinged plate, upon which the screw acts, as in an ordinary
vice. To bring this into use the freezing apparatus must be first removed,
and the embedding tube placed in the well, and firmly pressed into place.
Staining Animal Structures.
Specific stains are chiefly employed to assist the eye in distinguishing one
elementary tissue from another. It is therefore necessary to stain all
structures, as certain parts are seen to have a special affinity for one
colouring agent rather than another, whereby they become more deeply
stained, and consequently more clearly differentiated. For staining animal
structures, borax, carmine, and hæmatoxylin are more frequently employed
than others. The formulæ for each will be found in the Appendix “Formulæ
and Methods.”
Staining Process.—Place the section in distilled water to wash away the
alcohol; place a little of the carmine in a watch glass, and immerse the
section in it for four or five minutes; then remove it to a solution composed
Page 350
of methylated spirit five parts, hydrochloric acid one part; shake well
together. This solution should be kept ready for use. Immerse the section in
this solution and leave it to soak for about five or ten minutes if over-
stained, until the desired tint has been obtained. Sections of skin and fibrous
tissue may be left until nearly all colour is removed, the glands and hair
follicles will then be brought out more clearly. The section must be
transferred to methylated spirit to remove all traces of acid, then to oil of
cloves contained in a watch glass, lift the section from the methylated spirit
by one of the lifters (Fig. 250), and carefully float it on the oil, in which it
should be allowed to remain for about five minutes. This is the clearing
process, the object of which is to remove the spirit and prepare the section
for mounting in Canada balsam. First, however, place the section in filtered
turpentine to wash away the oil of cloves; this is found to answer better than
another plan adopted, that of removing the section from the oil of cloves
and mounting it in balsam direct. The oil, however, has a tendency to
darken the balsam.
Logwood or Hæmatoxylin Stains (see Appendix for the several formulæ).
Staining by this agent is effected as follows:—
After the specimen has been hardened in any of the chromic acid solutions
in use, transfer it to a seven per cent. watery solution of bicarbonate of soda
for about five minutes, then wash well in distilled water. Spirit prepared
preparations do not require to be transferred to the soda solution, but all
sections must be washed before they are transferred to the logwood stain.
To a watch glass nearly full of distilled water add ten or twenty drops of the
logwood stain, in which it should remain for twenty or thirty minutes. Wash
well with the ordinary tap water, which will fix the dye and cause it to
become blue. Dehydrate in methylated spirit, clear in clove oil, and mount
in dammar or Canada balsam.
Double-staining with Hæmatoxylin and Rosin.—Stain the section as
directed above, then place it in an alcoholic solution of rosin, about one
gramme of rosin to an ounce of methylated spirit, and let it soak for a few
minutes; wash well in methylated spirit, clear in oil of cloves, and mount in
balsam.
together. This solution should be kept ready for use. Immerse the section in
this solution and leave it to soak for about five or ten minutes if over-
stained, until the desired tint has been obtained. Sections of skin and fibrous
tissue may be left until nearly all colour is removed, the glands and hair
follicles will then be brought out more clearly. The section must be
transferred to methylated spirit to remove all traces of acid, then to oil of
cloves contained in a watch glass, lift the section from the methylated spirit
by one of the lifters (Fig. 250), and carefully float it on the oil, in which it
should be allowed to remain for about five minutes. This is the clearing
process, the object of which is to remove the spirit and prepare the section
for mounting in Canada balsam. First, however, place the section in filtered
turpentine to wash away the oil of cloves; this is found to answer better than
another plan adopted, that of removing the section from the oil of cloves
and mounting it in balsam direct. The oil, however, has a tendency to
darken the balsam.
Logwood or Hæmatoxylin Stains (see Appendix for the several formulæ).
Staining by this agent is effected as follows:—
After the specimen has been hardened in any of the chromic acid solutions
in use, transfer it to a seven per cent. watery solution of bicarbonate of soda
for about five minutes, then wash well in distilled water. Spirit prepared
preparations do not require to be transferred to the soda solution, but all
sections must be washed before they are transferred to the logwood stain.
To a watch glass nearly full of distilled water add ten or twenty drops of the
logwood stain, in which it should remain for twenty or thirty minutes. Wash
well with the ordinary tap water, which will fix the dye and cause it to
become blue. Dehydrate in methylated spirit, clear in clove oil, and mount
in dammar or Canada balsam.
Double-staining with Hæmatoxylin and Rosin.—Stain the section as
directed above, then place it in an alcoholic solution of rosin, about one
gramme of rosin to an ounce of methylated spirit, and let it soak for a few
minutes; wash well in methylated spirit, clear in oil of cloves, and mount in
balsam.
Page 351
Canada balsam should be prepared for use as follows:—One ounce of dried
balsam to one fluid ounce of pure benzole; dissolve, and keep in an outside
stoppered bottle. Clear the section in clove oil, and place it in turpentine,
clean a cover-glass and slide, place a few drops of balsam on the centre of
the latter, take the section from the turpentine on a lifter, allow the excess of
turpentine to drain away, and with a needle-point lift the section on to the
balsam slide. Now take up the cover-glass with a pair of forceps (Fig. 236),
and bring its edge in contact with the balsam, ease it down carefully as
shown in Fig. 237, so that no air bubbles are enclosed, and with the needle
point press the surface of the cover until the section lies quite smoothly and
flat, and the excess of balsam is pressed out. The slide should now be
transferred to the warm-chamber, and there allowed to remain for a day or
two, or until set and hardened.
Fig. 236.—Forceps for Mounting.
Any exuded balsam may be washed away with benzole and a soft camel’s
hair brush; then dry the slide with an old piece of linen cloth, and apply a
ring of cement or Japanner’s gold size. Other methods for staining and
mounting will be found to answer quite as well—that of Beneke’s is a
useful one for staining connective tissue.
Fig. 237.—Mode of placing Glass Cover on Object.
balsam to one fluid ounce of pure benzole; dissolve, and keep in an outside
stoppered bottle. Clear the section in clove oil, and place it in turpentine,
clean a cover-glass and slide, place a few drops of balsam on the centre of
the latter, take the section from the turpentine on a lifter, allow the excess of
turpentine to drain away, and with a needle-point lift the section on to the
balsam slide. Now take up the cover-glass with a pair of forceps (Fig. 236),
and bring its edge in contact with the balsam, ease it down carefully as
shown in Fig. 237, so that no air bubbles are enclosed, and with the needle
point press the surface of the cover until the section lies quite smoothly and
flat, and the excess of balsam is pressed out. The slide should now be
transferred to the warm-chamber, and there allowed to remain for a day or
two, or until set and hardened.
Fig. 236.—Forceps for Mounting.
Any exuded balsam may be washed away with benzole and a soft camel’s
hair brush; then dry the slide with an old piece of linen cloth, and apply a
ring of cement or Japanner’s gold size. Other methods for staining and
mounting will be found to answer quite as well—that of Beneke’s is a
useful one for staining connective tissue.
Fig. 237.—Mode of placing Glass Cover on Object.
Page 352
For staining connective tissue a modification of Weigert’s method of
staining fibrine is resorted to. Portions of tissue that have been fixed in
alcohol having been embedded in paraffin and cut, the sections are detached
and placed on glass slides, and stained for ten or twenty minutes with
gentian violet, ten parts, well shaken with water 100 parts; filter, and add
five to ten parts of a concentrated alcoholic gentian violet solution.
Afterwards treat for one minute with lugol solution, of a port wine tint, dry
with filter paper and decolourise with aniline xylol (aniline oil two parts
and xylol three parts). Decolourisation having been stopped at the right
point (judged from experience) mount the sections in xylol balsam. The
fibres of the connective tissue should appear stained of various shades of
violet.
Double Staining nucleated blood corpuscles. Two kinds of staining agents
are required. Stain A: dissolve five grammes of rosin in half an ounce of
distilled water, and add half an ounce of rectified alcohol. Stain B: dissolve
five grammes of methyl green in an ounce of distilled water. Place a drop of
frog’s blood on a glass slide, and with the edge of another slide spread it
evenly over the centre of the slip, and put it away to dry; when quite dry
flood the slide with stain A for three minutes, and wash with water, now
flood the slide with Stain B for five minutes, wash again with water, and
allow the slide to dry. Apply a drop of the prepared Canada balsam and a
cover-glass.
Fig. 238.—Shadbolt’s Turn-table.
staining fibrine is resorted to. Portions of tissue that have been fixed in
alcohol having been embedded in paraffin and cut, the sections are detached
and placed on glass slides, and stained for ten or twenty minutes with
gentian violet, ten parts, well shaken with water 100 parts; filter, and add
five to ten parts of a concentrated alcoholic gentian violet solution.
Afterwards treat for one minute with lugol solution, of a port wine tint, dry
with filter paper and decolourise with aniline xylol (aniline oil two parts
and xylol three parts). Decolourisation having been stopped at the right
point (judged from experience) mount the sections in xylol balsam. The
fibres of the connective tissue should appear stained of various shades of
violet.
Double Staining nucleated blood corpuscles. Two kinds of staining agents
are required. Stain A: dissolve five grammes of rosin in half an ounce of
distilled water, and add half an ounce of rectified alcohol. Stain B: dissolve
five grammes of methyl green in an ounce of distilled water. Place a drop of
frog’s blood on a glass slide, and with the edge of another slide spread it
evenly over the centre of the slip, and put it away to dry; when quite dry
flood the slide with stain A for three minutes, and wash with water, now
flood the slide with Stain B for five minutes, wash again with water, and
allow the slide to dry. Apply a drop of the prepared Canada balsam and a
cover-glass.
Fig. 238.—Shadbolt’s Turn-table.
Page 353
The blood of such mammals as are non-nucleated should be treated in a
slightly different way. Spread a drop or two of blood on a slide and dry it
quickly; then put the slide on Shadbolt’s turn-table (Fig. 238) and run a ring
of cement around it; allow this time to dry, and then apply a second coating,
and before this becomes quite dry place on it a clean glass cover, and press
it down gently with one of the fine needles (Fig. 229), until firmly adherent.
Epithelium.—Remove from the mouth of a frog by scraping some
squamous epithelium; the columnar must be taken from the stomach; place
it in glycerine, or Farrant’s solution on the slide; apply a cover-glass, and
with the point of the needle press it down until the epithelium cells are
separated and spread evenly over the slide. Set this aside for a day or two,
then wash away any of the medium which may have escaped; dry the slide,
and run a ring of cement around the edges, on the turn-table. Portions of the
intestine of a rabbit or other animal may be treated in the same way. If it is
wished to make permanent specimens of such structures, the intestine must
be hardened in a two per cent. solution of bichromate of potash for a couple
of days, then washed until all colour is discharged, and removed to a
solution of picro-carmine for twenty-four hours, after which allow the stain
to drain away, when it will be ready for mounting.
By the aid of the handy little spring clip (Fig. 239), objects of delicacy
when mounted may be left to dry and harden for any length of time.
Striped muscular fibre, taken from
the pig, must be teased out in a two
per cent. solution of bichromate of
potash, in which it should remain for
Fig. 239.—Spring-clip for Mounting. two or three weeks, when it may be
transferred to methylated spirit, and
allowed to remain until required for mounting. Soak a piece in water to
remove the spirit, place a small fragment on a slide in a few drops of water,
and with a couple of needles tease the tissue up, so as to separate the fibres.
Drain away the water, and apply a drop or two of Farrant’s medium and a
cover-glass, which cement down as before directed.
Fibrous tissue may be served in the same way. Yellow elastic tissue must be
first placed in a solution of chromic acid and spirit for ten days, and then
slightly different way. Spread a drop or two of blood on a slide and dry it
quickly; then put the slide on Shadbolt’s turn-table (Fig. 238) and run a ring
of cement around it; allow this time to dry, and then apply a second coating,
and before this becomes quite dry place on it a clean glass cover, and press
it down gently with one of the fine needles (Fig. 229), until firmly adherent.
Epithelium.—Remove from the mouth of a frog by scraping some
squamous epithelium; the columnar must be taken from the stomach; place
it in glycerine, or Farrant’s solution on the slide; apply a cover-glass, and
with the point of the needle press it down until the epithelium cells are
separated and spread evenly over the slide. Set this aside for a day or two,
then wash away any of the medium which may have escaped; dry the slide,
and run a ring of cement around the edges, on the turn-table. Portions of the
intestine of a rabbit or other animal may be treated in the same way. If it is
wished to make permanent specimens of such structures, the intestine must
be hardened in a two per cent. solution of bichromate of potash for a couple
of days, then washed until all colour is discharged, and removed to a
solution of picro-carmine for twenty-four hours, after which allow the stain
to drain away, when it will be ready for mounting.
By the aid of the handy little spring clip (Fig. 239), objects of delicacy
when mounted may be left to dry and harden for any length of time.
Striped muscular fibre, taken from
the pig, must be teased out in a two
per cent. solution of bichromate of
potash, in which it should remain for
Fig. 239.—Spring-clip for Mounting. two or three weeks, when it may be
transferred to methylated spirit, and
allowed to remain until required for mounting. Soak a piece in water to
remove the spirit, place a small fragment on a slide in a few drops of water,
and with a couple of needles tease the tissue up, so as to separate the fibres.
Drain away the water, and apply a drop or two of Farrant’s medium and a
cover-glass, which cement down as before directed.
Fibrous tissue may be served in the same way. Yellow elastic tissue must be
first placed in a solution of chromic acid and spirit for ten days, and then
Page 354
treated as directed for muscular fibre.
Non-striated Muscle.—A piece of the intestine of a rabbit should be steeped
in chromic acid and spirit for ten days, then washed in water; strip off a thin
layer of the muscular coat, and stain in hæmatoxylin solution. Well wash in
ordinary water until the colour changes to blue, when it will be fit for
mounting. Place a fragment on a slide and a drop of water, and carefully
separate the fibres with a pair of needles. Drain off the water, as it is now
ready for mounting, place on slide, and add a drop or two of Farrant’s
medium, and place on the cover-glass.
Nerve Tissue.—Dissect out the large sciatic nerve from a frog’s thigh, and
stretch it on a small piece of wood, to which pin both ends of the nerve, and
transfer it to a one per cent. solution of osmic acid for an hour or two. Wash
in distilled water; tease up a small fragment on a slide (as shown in Fig.
240), and apply a drop or two of Farrant’s solution and cover-glass.
Tissues containing air should be soaked in water that has been boiled for ten
minutes; this will displace the air. (For Farrant’s medium, see Appendix.)
Glycerine Jelly.—Dissolve one ounce of French gelatine in six ounces of
distilled water, and melt together in a hot-water bath. When quite dissolved,
add four ounces of glycerine, and a few drops of creosote or carbolic acid.
Filter through white filtering paper while warm, and keep in a capped
bottle. This may be used instead of Farrant’s solution.
Fig. 240.—Method of Teasing out Tissue.
Non-striated Muscle.—A piece of the intestine of a rabbit should be steeped
in chromic acid and spirit for ten days, then washed in water; strip off a thin
layer of the muscular coat, and stain in hæmatoxylin solution. Well wash in
ordinary water until the colour changes to blue, when it will be fit for
mounting. Place a fragment on a slide and a drop of water, and carefully
separate the fibres with a pair of needles. Drain off the water, as it is now
ready for mounting, place on slide, and add a drop or two of Farrant’s
medium, and place on the cover-glass.
Nerve Tissue.—Dissect out the large sciatic nerve from a frog’s thigh, and
stretch it on a small piece of wood, to which pin both ends of the nerve, and
transfer it to a one per cent. solution of osmic acid for an hour or two. Wash
in distilled water; tease up a small fragment on a slide (as shown in Fig.
240), and apply a drop or two of Farrant’s solution and cover-glass.
Tissues containing air should be soaked in water that has been boiled for ten
minutes; this will displace the air. (For Farrant’s medium, see Appendix.)
Glycerine Jelly.—Dissolve one ounce of French gelatine in six ounces of
distilled water, and melt together in a hot-water bath. When quite dissolved,
add four ounces of glycerine, and a few drops of creosote or carbolic acid.
Filter through white filtering paper while warm, and keep in a capped
bottle. This may be used instead of Farrant’s solution.
Fig. 240.—Method of Teasing out Tissue.
Page 355
Nitrate of silver darkens by exposure; it is used in a half per cent. watery
solution. Specimens to be acted upon should be washed in distilled water, to
remove every trace of sodium chloride, and then steeped in the silver
solution for some two or three minutes, after which they should be again
washed until they cease to turn milky; then place them in glycerine and
expose them to the action of light until they assume a dark brown colour,
when they should be mounted in glycerine or glycerine jelly.
By means of this stain the endothelial cells of the lymphatics, blood vessels,
&c., and the nodes of Ranvier, constrictions in medullary nerves, are
rendered visible. Sections of any of these may subsequently be stained by
logwood or carmine.
Several methods have been adopted for staining with gold chloride. Dr.
Klein’s and Professor Schäfer’s are among the best.
Dr. Klein’s method of showing the nerves of the cornea is as follows:—
Remove the cornea within fifteen minutes of death; place it in a half per
cent. chloride of gold solution for half an hour, or an hour; wash in distilled
water, and expose to the light for a few days; in the meantime occasionally
change the water. Then immerse it in glycerine and distilled water, in the
proportion of one to two; lastly, place it in water, and brush gently with a
sable pencil to remove any precipitate, when it will be fit for mounting in
glycerine. The colour of the cornea should be grey-violet.
Schäfer adopts another method—a double chloride of gold and potassium
solution.
Osmic acid, first used by Schultze, is useful for the demonstration of fatty
matters, all of which it colours black; it is also valuable for certain nerve
preparations. Specimens should be allowed to remain in a one or two per
cent. aqueous solution of the acid from a quarter to twenty-four hours, when
the staining will be completed; but if it is desired to harden specimens at the
same time, they should remain in it for some few days. Osmic acid does not
penetrate very deeply, therefore small portions should be selected for
immersion. This is a useful stain for infusorial animals.
solution. Specimens to be acted upon should be washed in distilled water, to
remove every trace of sodium chloride, and then steeped in the silver
solution for some two or three minutes, after which they should be again
washed until they cease to turn milky; then place them in glycerine and
expose them to the action of light until they assume a dark brown colour,
when they should be mounted in glycerine or glycerine jelly.
By means of this stain the endothelial cells of the lymphatics, blood vessels,
&c., and the nodes of Ranvier, constrictions in medullary nerves, are
rendered visible. Sections of any of these may subsequently be stained by
logwood or carmine.
Several methods have been adopted for staining with gold chloride. Dr.
Klein’s and Professor Schäfer’s are among the best.
Dr. Klein’s method of showing the nerves of the cornea is as follows:—
Remove the cornea within fifteen minutes of death; place it in a half per
cent. chloride of gold solution for half an hour, or an hour; wash in distilled
water, and expose to the light for a few days; in the meantime occasionally
change the water. Then immerse it in glycerine and distilled water, in the
proportion of one to two; lastly, place it in water, and brush gently with a
sable pencil to remove any precipitate, when it will be fit for mounting in
glycerine. The colour of the cornea should be grey-violet.
Schäfer adopts another method—a double chloride of gold and potassium
solution.
Osmic acid, first used by Schultze, is useful for the demonstration of fatty
matters, all of which it colours black; it is also valuable for certain nerve
preparations. Specimens should be allowed to remain in a one or two per
cent. aqueous solution of the acid from a quarter to twenty-four hours, when
the staining will be completed; but if it is desired to harden specimens at the
same time, they should remain in it for some few days. Osmic acid does not
penetrate very deeply, therefore small portions should be selected for
immersion. This is a useful stain for infusorial animals.
Page 356
Chloride of palladium, another of Schultze’s staining fluids, is used to stain
and harden the retina, crystalline lens, and other tissues of the eye, the
cornified fat and connective tissues remaining uncoloured. The solution
should be used very weak:—Chloride of palladium, one part; distilled
water, 1,000 parts. Specimens should be mounted in glycerine at once, or
further stained with carmine.
Dr. Schäfer employs a silver nitrate and gelatine solution for demonstrating
lung epithelium; this is made as follows:—Take of gelatine ten grammes,
soak in cold water, dissolve, and add warm water to 100 cc. Dissolve a
decigramme of nitrate of silver in a little distilled water, and add to the
gelatine solution. Inject this with a glass syringe into the lung until
distension is pretty complete. Leave it to rest in a cool place until the
gelatine has set; then cut sections as thin as possible, place them on a slide
with glycerine, and expose to light till ready for mounting.
Of the double stains Mr. Groves prefers only those where the double colour
is produced by a single process—or stains in which one colour is first
employed, and then another. Single stains are picro-carmine, carmine and
indigo carmine, aniline blue and aniline red.
Picro-carmine is specially useful for staining sections hardened in picric
acid. It is prepared in several ways:—
1. Add to a saturated solution of picric acid in water a strong solution of
carmine in ammonia to saturation.
2. Evaporate the mixture to one-fifth its bulk over a water bath, allow it to
cool, filter from deposit, and evaporate to dryness, when picro-carmine is
left as a crystalline powder of red-ochre colour.
Sections can be stained in a one per cent. aqueous solution, requiring only
ten minutes for the process; wash well in distilled water, and transfer them
to methylated alcohol, then to absolute alcohol, after which they are
rendered transparent by immersing in oil of cloves or benzole, before
mounting in balsam or dammar.
To summarise Mr. Groves’ recommendations:—
and harden the retina, crystalline lens, and other tissues of the eye, the
cornified fat and connective tissues remaining uncoloured. The solution
should be used very weak:—Chloride of palladium, one part; distilled
water, 1,000 parts. Specimens should be mounted in glycerine at once, or
further stained with carmine.
Dr. Schäfer employs a silver nitrate and gelatine solution for demonstrating
lung epithelium; this is made as follows:—Take of gelatine ten grammes,
soak in cold water, dissolve, and add warm water to 100 cc. Dissolve a
decigramme of nitrate of silver in a little distilled water, and add to the
gelatine solution. Inject this with a glass syringe into the lung until
distension is pretty complete. Leave it to rest in a cool place until the
gelatine has set; then cut sections as thin as possible, place them on a slide
with glycerine, and expose to light till ready for mounting.
Of the double stains Mr. Groves prefers only those where the double colour
is produced by a single process—or stains in which one colour is first
employed, and then another. Single stains are picro-carmine, carmine and
indigo carmine, aniline blue and aniline red.
Picro-carmine is specially useful for staining sections hardened in picric
acid. It is prepared in several ways:—
1. Add to a saturated solution of picric acid in water a strong solution of
carmine in ammonia to saturation.
2. Evaporate the mixture to one-fifth its bulk over a water bath, allow it to
cool, filter from deposit, and evaporate to dryness, when picro-carmine is
left as a crystalline powder of red-ochre colour.
Sections can be stained in a one per cent. aqueous solution, requiring only
ten minutes for the process; wash well in distilled water, and transfer them
to methylated alcohol, then to absolute alcohol, after which they are
rendered transparent by immersing in oil of cloves or benzole, before
mounting in balsam or dammar.
To summarise Mr. Groves’ recommendations:—
Page 357
1. Let the material be quite fresh.
2. (a) Take care that the hardening or softening fluid is not too strong. (b)
Use a large bulk of fluid in proportion to the material. (c) Change the fluid
frequently. (d) If freezing be employed, take care that the specimen is
thoroughly frozen.
3. (a) Always use a sharp razor. (b) Take it with one diagonal sweep through
the material. (c) Make the sections as thin as possible; and (d) Remove each
one as soon as cut, for if sections accumulate on the knife or razor they are
sure to get torn.
4. (a) Do not be in a hurry to stain, but (b) Remember that a weak colouring
solution permeates the section better, and produces the best results; and (c)
That the thinner the section the better it will take the stains.
5. (a) Always use glass slips and covers free from scratches and bubbles,
and chemically clean. (b) Never use any but extra thin circular covers, so
that the specimens may be used with high powers. (c) Always use cold
preservatives, except in the case of glycerine jelly, and never use warmth to
hasten the drying of balsam or dammar, but run a ring of cement round the
cover.
6. Label specimens correctly; keep them in a flat tray, and in the dark.
Double and Treble Staining.
Dr. W. Stirling46 furnishes a brief but useful account of the methods he has
employed with much success.
Osmic Acid and Picro-carmine.—Mix on a glass slide a drop of the blood
of newt or frog and a drop of a one per cent. aqueous solution of osmic
acid, and allow the slide to stand by. This will fix the corpuscles without
altering their shape. At the end of five minutes remove any excess of acid
with blotting-paper, add a drop of a solution of picro-carmine, and a trace of
glycerine to prevent evaporation, and set aside for three or four hours to see
2. (a) Take care that the hardening or softening fluid is not too strong. (b)
Use a large bulk of fluid in proportion to the material. (c) Change the fluid
frequently. (d) If freezing be employed, take care that the specimen is
thoroughly frozen.
3. (a) Always use a sharp razor. (b) Take it with one diagonal sweep through
the material. (c) Make the sections as thin as possible; and (d) Remove each
one as soon as cut, for if sections accumulate on the knife or razor they are
sure to get torn.
4. (a) Do not be in a hurry to stain, but (b) Remember that a weak colouring
solution permeates the section better, and produces the best results; and (c)
That the thinner the section the better it will take the stains.
5. (a) Always use glass slips and covers free from scratches and bubbles,
and chemically clean. (b) Never use any but extra thin circular covers, so
that the specimens may be used with high powers. (c) Always use cold
preservatives, except in the case of glycerine jelly, and never use warmth to
hasten the drying of balsam or dammar, but run a ring of cement round the
cover.
6. Label specimens correctly; keep them in a flat tray, and in the dark.
Double and Treble Staining.
Dr. W. Stirling46 furnishes a brief but useful account of the methods he has
employed with much success.
Osmic Acid and Picro-carmine.—Mix on a glass slide a drop of the blood
of newt or frog and a drop of a one per cent. aqueous solution of osmic
acid, and allow the slide to stand by. This will fix the corpuscles without
altering their shape. At the end of five minutes remove any excess of acid
with blotting-paper, add a drop of a solution of picro-carmine, and a trace of
glycerine to prevent evaporation, and set aside for three or four hours to see
Page 358
that no overstaining takes place. At the end of this time the nucleus will be
found to be stained red, and the perinuclear part yellow.
Picric Acid and Picro-carmine.—Place a drop of the blood of a frog or
newt on a glass slide, and add a drop of a saturated solution of picric acid:
put the slide aside and allow it to remain for five minutes; at the end of that
time, when the acid has fixed the corpuscles (that is, coagulated their
contents), any excess of acid should be removed as before. A drop of
solution of picro-carmine should now be added, and a trace of glycerine,
and the preparation set aside for an hour. At the end of that time remove the
picro-carmine solution by means of a narrow slip of blotting-paper, and add
a drop of Farrant’s solution of glycerine and apply glass-cover. The
perinuclear part of the corpuscles will be seen to be highly granular and of a
deep orange colour, whilst the nucleus is stained red. Some of the
corpuscles will appear of a delicate yellow colour, and threads are seen
extending from the nucleus to the envelopes. The preparation should be
preserved and mounted in glycerine.
Picro-carmine and Aniline Dye.—For glandular tissue, none of the aniline
dyes answer so well as iodine green, used in the form of a one per cent.
watery solution. Stain the tissue in picro-carmine, wash it in distilled water
acidulated with acetic acid, and stain it in a solution of iodine green. As it
acts rapidly, care must be taken not to overstain. Wash the section in water,
and then transfer it to alcohol; finally clear with oil of cloves. The washing
should be done rapidly, as the spirit dissolves out the green dye. All
preparations stained with iodine green must be mounted in dammar.
Picro-carmine and Iodine Green.—Stain a section of the cancellated head
of a very young bone (fœtal bone) in picro-carmine, wash it in distilled
water, and stain it with iodine green, and mount in dammar. All newly-
formed bone is stained red; that in the centre of the osseous trabeculæ, the
residue of the calcified cartilage in which the bone is deposited, is stained
green. Many of the bone corpuscles are also stained green.
Ossifying cartilage, the back part of the tongue, Peyer’s Patches, solitary-
glands, trachea, and bronchus, may all be treated in the same way. In
preparing the skin, take a vertical section from the sole of the foot of a
fœtus. The cuticle and superficial layers of the epithelium are dyed yellow,
found to be stained red, and the perinuclear part yellow.
Picric Acid and Picro-carmine.—Place a drop of the blood of a frog or
newt on a glass slide, and add a drop of a saturated solution of picric acid:
put the slide aside and allow it to remain for five minutes; at the end of that
time, when the acid has fixed the corpuscles (that is, coagulated their
contents), any excess of acid should be removed as before. A drop of
solution of picro-carmine should now be added, and a trace of glycerine,
and the preparation set aside for an hour. At the end of that time remove the
picro-carmine solution by means of a narrow slip of blotting-paper, and add
a drop of Farrant’s solution of glycerine and apply glass-cover. The
perinuclear part of the corpuscles will be seen to be highly granular and of a
deep orange colour, whilst the nucleus is stained red. Some of the
corpuscles will appear of a delicate yellow colour, and threads are seen
extending from the nucleus to the envelopes. The preparation should be
preserved and mounted in glycerine.
Picro-carmine and Aniline Dye.—For glandular tissue, none of the aniline
dyes answer so well as iodine green, used in the form of a one per cent.
watery solution. Stain the tissue in picro-carmine, wash it in distilled water
acidulated with acetic acid, and stain it in a solution of iodine green. As it
acts rapidly, care must be taken not to overstain. Wash the section in water,
and then transfer it to alcohol; finally clear with oil of cloves. The washing
should be done rapidly, as the spirit dissolves out the green dye. All
preparations stained with iodine green must be mounted in dammar.
Picro-carmine and Iodine Green.—Stain a section of the cancellated head
of a very young bone (fœtal bone) in picro-carmine, wash it in distilled
water, and stain it with iodine green, and mount in dammar. All newly-
formed bone is stained red; that in the centre of the osseous trabeculæ, the
residue of the calcified cartilage in which the bone is deposited, is stained
green. Many of the bone corpuscles are also stained green.
Ossifying cartilage, the back part of the tongue, Peyer’s Patches, solitary-
glands, trachea, and bronchus, may all be treated in the same way. In
preparing the skin, take a vertical section from the sole of the foot of a
fœtus. The cuticle and superficial layers of the epithelium are dyed yellow,
Page 359
the rete Malpighii green; and the continuation of these cells can be traced
into the ducts of the sweat-glands, which are green, and form a marked
contrast to the red stained connective tissue of the cutis vera, through which
they have to ascend to reach the surface. The outer layer of the grey matter
of the cerebellum with Purkinge’s cells is, when double stained, red, while
the inner or granular layer is green. Logwood and iodine green stains the
mucous glands of the tongue green, and the serous glands, lilac logwood
stain.
Eosin and Iodine Green.—Eosin is used as the ground colour. Stain the
tissue in an alcoholic solution of eosin, which will colour it very rapidly,
usually in a few seconds. Wash the section thoroughly in water acidulated
with acetic or hydrochloric acid, a one per cent. solution, and stain with
iodine green. This will double stain bone and cerebellum; but if logwood is
substituted for the latter, the cerebrum and general substance become
stained by the eosin, while the logwood colours the nerve-cells a lilac.
Gold Chloride and Aniline Dyes.—The tissue must be impregnated with
chloride of gold, and then stained with either aniline blue, iodine green, or
rosin. The tail of a young rat, containing as it does so many different
structures, is an excellent material for experimenting upon. Remove the
skin from the tail, and place pieces half an inch long into the juice of a fresh
lemon for five minutes, wash it to get rid of the acid. The fine tendons swell
up under the action of the lemon acid, and permit of the more ready action
of the chloride of gold solution. Place the piece for an hour or more in a one
per cent. solution of gold, remove it and wash it thoroughly, and then place
it in a twenty-five per cent. solution of formic acid for twenty-four hours.
This reduces the gold. During the process of reduction the preparation must
be kept in the dark. The osseous portion has then to be decalcified in the
ordinary way, with a mixture of chromic and nitric acid. After
decalcification preserve the whole in alcohol. Transverse sections of the
decalcified tail are made, and may be stained with a red dye, as rosin, and
afterwards with a watery solution of iodine green. Mount in dammar.
Injecting Small Animal Bodies.
into the ducts of the sweat-glands, which are green, and form a marked
contrast to the red stained connective tissue of the cutis vera, through which
they have to ascend to reach the surface. The outer layer of the grey matter
of the cerebellum with Purkinge’s cells is, when double stained, red, while
the inner or granular layer is green. Logwood and iodine green stains the
mucous glands of the tongue green, and the serous glands, lilac logwood
stain.
Eosin and Iodine Green.—Eosin is used as the ground colour. Stain the
tissue in an alcoholic solution of eosin, which will colour it very rapidly,
usually in a few seconds. Wash the section thoroughly in water acidulated
with acetic or hydrochloric acid, a one per cent. solution, and stain with
iodine green. This will double stain bone and cerebellum; but if logwood is
substituted for the latter, the cerebrum and general substance become
stained by the eosin, while the logwood colours the nerve-cells a lilac.
Gold Chloride and Aniline Dyes.—The tissue must be impregnated with
chloride of gold, and then stained with either aniline blue, iodine green, or
rosin. The tail of a young rat, containing as it does so many different
structures, is an excellent material for experimenting upon. Remove the
skin from the tail, and place pieces half an inch long into the juice of a fresh
lemon for five minutes, wash it to get rid of the acid. The fine tendons swell
up under the action of the lemon acid, and permit of the more ready action
of the chloride of gold solution. Place the piece for an hour or more in a one
per cent. solution of gold, remove it and wash it thoroughly, and then place
it in a twenty-five per cent. solution of formic acid for twenty-four hours.
This reduces the gold. During the process of reduction the preparation must
be kept in the dark. The osseous portion has then to be decalcified in the
ordinary way, with a mixture of chromic and nitric acid. After
decalcification preserve the whole in alcohol. Transverse sections of the
decalcified tail are made, and may be stained with a red dye, as rosin, and
afterwards with a watery solution of iodine green. Mount in dammar.
Injecting Small Animal Bodies.
Page 360
Fig. 241.—Injecting Syringe. Fig. 242.—Water Bath and Melting Vessels.
The injection of animal bodies practised by the older anatomists, to render
the vascular system more apparent, has not been superseded by the more
modern methods of staining. The method of injecting even small bodies
requires some skill, and a few pieces of apparatus made expressly for the
purpose. First, a special form of brass syringe of such a size that it may be
grasped with the right hand, the thumb at the same time covering the button
at the top of the piston-rod when drawn out to the full. In Fig. 241 the
piston rod is seen withdrawn, a is the body, with a screw at the top for
firmly screwing down the cover, b, after the piston, c, is replaced; e is a
stop-cock, to the end of which either of the smaller cannulæ, g, is affixed.
The transverse wires are for securing them tightly with thread to the vessels
into which they are to be inserted. In addition to the syringe, two or three
tinned vessels are required to contain size, injecting fluid, and hot water.
The size must be kept hot by the aid of a water bath; if a naked fire be used
there is danger of burning it. A convenient form of apparatus for melting the
The injection of animal bodies practised by the older anatomists, to render
the vascular system more apparent, has not been superseded by the more
modern methods of staining. The method of injecting even small bodies
requires some skill, and a few pieces of apparatus made expressly for the
purpose. First, a special form of brass syringe of such a size that it may be
grasped with the right hand, the thumb at the same time covering the button
at the top of the piston-rod when drawn out to the full. In Fig. 241 the
piston rod is seen withdrawn, a is the body, with a screw at the top for
firmly screwing down the cover, b, after the piston, c, is replaced; e is a
stop-cock, to the end of which either of the smaller cannulæ, g, is affixed.
The transverse wires are for securing them tightly with thread to the vessels
into which they are to be inserted. In addition to the syringe, two or three
tinned vessels are required to contain size, injecting fluid, and hot water.
The size must be kept hot by the aid of a water bath; if a naked fire be used
there is danger of burning it. A convenient form of apparatus for melting the
Page 361
size, and afterwards keeping it at a proper temperature, is Fig. 242.
Fig. 243.—Artery Needle.
A pair of strong forceps for seizing the vessel, and a small needle (Fig. 243)
is also necessary for passing the thread round the vessel into which the
injection pipe has been inserted. These complete the list of apparatus. To
prepare the material for opaque injections, take one pound of the finest and
most transparent glue, break it into small pieces, put it into an earthen pot,
and pour on it three pints of cold water; let it stand twenty-four hours,
stirring it now and then with a stick; set it over a slow fire for half an hour,
or until all the pieces are perfectly dissolved, skim off the froth from the
surface, and strain through a flannel for use. Isinglass and cuttings of
parchment make an excellent size, and are preferable for particular
injections. If gelatine be employed an ounce to a pint of water will be
sufficiently strong, but in very hot weather it is necessary to add a little
more gelatine. It must be first soaked in part of the cold water until it swells
up and becomes soft, when the rest of the water, made hot, is to be added.
The size thus prepared may be fixed with finely levigated vermilion,
chrome-yellow, blue salts, or flake white.
To prepare the subject, the principal points to be attained are: to dissolve the
fluids and completely empty the vessels; relax the solids; and prevent the
injection from coagulating too soon. For this purpose it is necessary to place
the animal, or part to be injected, in warm water, as hot as the operator’s
hand will bear. This should be kept at nearly the same temperature for some
time by occasionally adding hot water. The length of time required is in
proportion to the size of the part and the amount of its rigidity.
Injecting the systems of Vessels with different colours: Carmine and
Gelatine Injection.—Carmine 30 grains, strong liquid ammonia 60 drops,
glacial acetic acid 43 drops, gelatine solution (one ounce in six ounces of
water) two ounces, water one ounce: dissolve the carmine in the ammonia
and water in a test tube, and mix it with one half of the warm gelatine, add
Fig. 243.—Artery Needle.
A pair of strong forceps for seizing the vessel, and a small needle (Fig. 243)
is also necessary for passing the thread round the vessel into which the
injection pipe has been inserted. These complete the list of apparatus. To
prepare the material for opaque injections, take one pound of the finest and
most transparent glue, break it into small pieces, put it into an earthen pot,
and pour on it three pints of cold water; let it stand twenty-four hours,
stirring it now and then with a stick; set it over a slow fire for half an hour,
or until all the pieces are perfectly dissolved, skim off the froth from the
surface, and strain through a flannel for use. Isinglass and cuttings of
parchment make an excellent size, and are preferable for particular
injections. If gelatine be employed an ounce to a pint of water will be
sufficiently strong, but in very hot weather it is necessary to add a little
more gelatine. It must be first soaked in part of the cold water until it swells
up and becomes soft, when the rest of the water, made hot, is to be added.
The size thus prepared may be fixed with finely levigated vermilion,
chrome-yellow, blue salts, or flake white.
To prepare the subject, the principal points to be attained are: to dissolve the
fluids and completely empty the vessels; relax the solids; and prevent the
injection from coagulating too soon. For this purpose it is necessary to place
the animal, or part to be injected, in warm water, as hot as the operator’s
hand will bear. This should be kept at nearly the same temperature for some
time by occasionally adding hot water. The length of time required is in
proportion to the size of the part and the amount of its rigidity.
Injecting the systems of Vessels with different colours: Carmine and
Gelatine Injection.—Carmine 30 grains, strong liquid ammonia 60 drops,
glacial acetic acid 43 drops, gelatine solution (one ounce in six ounces of
water) two ounces, water one ounce: dissolve the carmine in the ammonia
and water in a test tube, and mix it with one half of the warm gelatine, add
Page 362
the acid to the remaining half of gelatine, and drop it little by little into the
carmine mixture, stirring it well with a glass rod during the mixing; filter
through flannel, and add a few drops of carbolic acid to make it keep. It is
very important that the stain should be quite neutral, the test of which is the
colour and smell of the fluid. It should be a bright red, and all trace of smell
of ammonia must be removed.
Prussian or Berlin Blue and Gelatine.—Take 1½ ounces of gelatine, place
it in a vessel and cover it with water; allow it to stand until all the water is
absorbed and the gelatine is quite soft, then dissolve in hot water. Dissolve
one drachm (60 grains) of Prussian or Berlin blue in six ounces of water,
and gradually mix it with the gelatine solution, stirring well with a glass rod
during the mixing; then filter as before.
Watery Solution of Berlin Blue.—Dissolve 2½ drachms of the blue in 18
ounces of distilled water, and filter. This staining fluid is used for injecting
the lymphatic system.
Directions for Injecting.—The animal to be injected must be first killed by
chloroform, and injected while still warm; to secure this place the body in a
water bath, at a temperature of 104° Fahrenheit. Expose the main artery of
the parts to be injected, clear a small portion of it from the surrounding
tissues, and place a ligature of thin tissue or silk round it, by means of the
small artery needle (Fig. 243). With a pair of sharp-pointed scissors make
an oblique slit in the wall of the vessel, insert the cannula, and tie the
ligature firmly over the artery behind the point of the cannula, into which
put the stop-cock. Fill the syringe with injection fluid, which must not be
too warm, and take care not to draw up any air-bubbles; insert the nozzle of
the syringe into the stop-cock and force in a little fluid; remove the syringe
so that the air may escape, re-insert the syringe, repeat the process until no
air-bubbles escape, and then proceed slowly with the injection. Half an hour
will be required to complete the process in an animal the size of a rabbit. To
judge of the completeness of the injection, examine the vascular parts of the
lips, tongues and eyes; if satisfactory, tie the ligature round the artery and
withdraw the syringe; place the animal in cold water for an hour to
consolidate the injection fluid. When cold dissect out the organs, cut them
up, and place them in methylated spirit to harden. Change the spirit every
carmine mixture, stirring it well with a glass rod during the mixing; filter
through flannel, and add a few drops of carbolic acid to make it keep. It is
very important that the stain should be quite neutral, the test of which is the
colour and smell of the fluid. It should be a bright red, and all trace of smell
of ammonia must be removed.
Prussian or Berlin Blue and Gelatine.—Take 1½ ounces of gelatine, place
it in a vessel and cover it with water; allow it to stand until all the water is
absorbed and the gelatine is quite soft, then dissolve in hot water. Dissolve
one drachm (60 grains) of Prussian or Berlin blue in six ounces of water,
and gradually mix it with the gelatine solution, stirring well with a glass rod
during the mixing; then filter as before.
Watery Solution of Berlin Blue.—Dissolve 2½ drachms of the blue in 18
ounces of distilled water, and filter. This staining fluid is used for injecting
the lymphatic system.
Directions for Injecting.—The animal to be injected must be first killed by
chloroform, and injected while still warm; to secure this place the body in a
water bath, at a temperature of 104° Fahrenheit. Expose the main artery of
the parts to be injected, clear a small portion of it from the surrounding
tissues, and place a ligature of thin tissue or silk round it, by means of the
small artery needle (Fig. 243). With a pair of sharp-pointed scissors make
an oblique slit in the wall of the vessel, insert the cannula, and tie the
ligature firmly over the artery behind the point of the cannula, into which
put the stop-cock. Fill the syringe with injection fluid, which must not be
too warm, and take care not to draw up any air-bubbles; insert the nozzle of
the syringe into the stop-cock and force in a little fluid; remove the syringe
so that the air may escape, re-insert the syringe, repeat the process until no
air-bubbles escape, and then proceed slowly with the injection. Half an hour
will be required to complete the process in an animal the size of a rabbit. To
judge of the completeness of the injection, examine the vascular parts of the
lips, tongues and eyes; if satisfactory, tie the ligature round the artery and
withdraw the syringe; place the animal in cold water for an hour to
consolidate the injection fluid. When cold dissect out the organs, cut them
up, and place them in methylated spirit to harden. Change the spirit every
Page 363
twenty-four hours for the first three days. The hardening process will be
complete in ten days.
To inject lymphatics by the puncture process, a small-sized subcutaneous
syringe should be used, filled with a watery solution of the prepared stains.
Thrust the nozzle into the pad of the foot, (or tongue), and then rub the limb
to cause the injection fluid to flow along the lymphatic vessels into the
glands.
When the blue stain is used add a few drops of acetic acid to the spirit while
the hardening process is going on.
Of Injecting Different Systems of Vessels with Different Colours.—It is often
desirable to inject different systems of vessels distributed to a part with
different colours, in order to ascertain the arrangement of each set of vessels
and their relation to each other. A portion of the gall-bladder in which the
veins have been injected with white lead, and the arteries with vermilion,
forms an attractive preparation. Each artery, even to its smallest branches, is
seen to be accompanied by two small veins, one lying on either side of it.
By this method four different sets of tubes have been injected—the artery
with vermilion, the portal vein with white lead, the duct with Prussian blue,
and the hepatic vein with lake. There are also opaque colouring matters
which may be employed for double injections.
Injecting the Lower Animals.—The vessels of fishes are exceedingly tender,
and require great caution in filling them. It is often difficult or quite
impossible to tie the pipe in the vessel of a fish, and it will generally be
found a much easier process to cut off the tail of the fish, and put the pipe
into the divided vessel which lies immediately beneath the spinal column.
In this simple manner beautiful injections of fish may be made.
Mollusca (slug, snail, oyster, &c.).—The tenuity of the vessels of the
mollusc often renders it impossible to tie the pipe in the usual manner. The
capillaries are, however, usually very large, so that the injection runs very
readily. In different parts of the bodies of these animals are numerous
lacunæ or spaces, which communicate directly with the vessels. Now, if an
opening be made through the integument of the muscular foot of the animal,
complete in ten days.
To inject lymphatics by the puncture process, a small-sized subcutaneous
syringe should be used, filled with a watery solution of the prepared stains.
Thrust the nozzle into the pad of the foot, (or tongue), and then rub the limb
to cause the injection fluid to flow along the lymphatic vessels into the
glands.
When the blue stain is used add a few drops of acetic acid to the spirit while
the hardening process is going on.
Of Injecting Different Systems of Vessels with Different Colours.—It is often
desirable to inject different systems of vessels distributed to a part with
different colours, in order to ascertain the arrangement of each set of vessels
and their relation to each other. A portion of the gall-bladder in which the
veins have been injected with white lead, and the arteries with vermilion,
forms an attractive preparation. Each artery, even to its smallest branches, is
seen to be accompanied by two small veins, one lying on either side of it.
By this method four different sets of tubes have been injected—the artery
with vermilion, the portal vein with white lead, the duct with Prussian blue,
and the hepatic vein with lake. There are also opaque colouring matters
which may be employed for double injections.
Injecting the Lower Animals.—The vessels of fishes are exceedingly tender,
and require great caution in filling them. It is often difficult or quite
impossible to tie the pipe in the vessel of a fish, and it will generally be
found a much easier process to cut off the tail of the fish, and put the pipe
into the divided vessel which lies immediately beneath the spinal column.
In this simple manner beautiful injections of fish may be made.
Mollusca (slug, snail, oyster, &c.).—The tenuity of the vessels of the
mollusc often renders it impossible to tie the pipe in the usual manner. The
capillaries are, however, usually very large, so that the injection runs very
readily. In different parts of the bodies of these animals are numerous
lacunæ or spaces, which communicate directly with the vessels. Now, if an
opening be made through the integument of the muscular foot of the animal,
Page 364
a pipe may be inserted, and thus the vessels may be injected from these
lacunæ with comparative facility.
Insects.—Injections of insects may be made by forcing the injection into the
general abdominal cavity, when it passes into the dorsal vessel and is
afterwards distributed throughout the system. The superfluous injection is
then washed away, and such parts of the body as may be required removed
for examination.
Natural injection of Medusæ may be effected without injuring the vessels,
with an opening at the side remote from it. The medusa must be placed in a
glass vessel, with the bell downwards, and a bell-jar ending in a narrow
tube above is placed over it and made air-tight; the medusa is then covered
with the injection-mass, the air in the glass is exhausted, and as the sea-
water runs out by slits in the lower side of the annular canal, the coloured
fluid runs in. In the case of leeches and large species of earthworms, the
natural injection is made from the ventral sinus. In all cases a glass tube is
used, with a finely drawn-out point. The injection is complete when the
injection issues from the counter-opening. Besides the animals mentioned,
large caterpillars, beetles, and larvæ of various kinds are favourable objects
for injection; the glass cannula being introduced into the posterior end of
the dorsal vessel, and the counter-opening made in the ventral vessel, and
vice versâ.
Staining Living Protoplasm with Bismarck Brown.—Henneguy having
treated Paramœcium aurelia with an aqueous solution of aniline brown
(known as “Bismarck Brown”), found that they assumed an intense yellow-
brown colour. The colour first appears in the vacuoles of the protoplasm,
and then in the protoplasm itself, the nucleus generally remaining
colourless, and becoming more visible than in the normal state. If a yellow-
tinted paramœcium be compressed so as to cause a small quantity of the
protoplasm to exude, it is seen that it really is the protoplasmic substance
which becomes coloured. All the Infusoria may be stained with Bismarck
brown, but no other aniline colour employed exhibits the same property—
they merely stain the Infusoria after death, and are in fact poisonous. Living
protoplasm does not as a rule absorb colouring matters, and as Infusoria are
chiefly composed of protoplasm, attempts have been made to ascertain
lacunæ with comparative facility.
Insects.—Injections of insects may be made by forcing the injection into the
general abdominal cavity, when it passes into the dorsal vessel and is
afterwards distributed throughout the system. The superfluous injection is
then washed away, and such parts of the body as may be required removed
for examination.
Natural injection of Medusæ may be effected without injuring the vessels,
with an opening at the side remote from it. The medusa must be placed in a
glass vessel, with the bell downwards, and a bell-jar ending in a narrow
tube above is placed over it and made air-tight; the medusa is then covered
with the injection-mass, the air in the glass is exhausted, and as the sea-
water runs out by slits in the lower side of the annular canal, the coloured
fluid runs in. In the case of leeches and large species of earthworms, the
natural injection is made from the ventral sinus. In all cases a glass tube is
used, with a finely drawn-out point. The injection is complete when the
injection issues from the counter-opening. Besides the animals mentioned,
large caterpillars, beetles, and larvæ of various kinds are favourable objects
for injection; the glass cannula being introduced into the posterior end of
the dorsal vessel, and the counter-opening made in the ventral vessel, and
vice versâ.
Staining Living Protoplasm with Bismarck Brown.—Henneguy having
treated Paramœcium aurelia with an aqueous solution of aniline brown
(known as “Bismarck Brown”), found that they assumed an intense yellow-
brown colour. The colour first appears in the vacuoles of the protoplasm,
and then in the protoplasm itself, the nucleus generally remaining
colourless, and becoming more visible than in the normal state. If a yellow-
tinted paramœcium be compressed so as to cause a small quantity of the
protoplasm to exude, it is seen that it really is the protoplasmic substance
which becomes coloured. All the Infusoria may be stained with Bismarck
brown, but no other aniline colour employed exhibits the same property—
they merely stain the Infusoria after death, and are in fact poisonous. Living
protoplasm does not as a rule absorb colouring matters, and as Infusoria are
chiefly composed of protoplasm, attempts have been made to ascertain
Page 365
whether protoplasm in general, of animal or vegetable origin, behaved in
the same way in the presence of aniline brown. A tolerably strong solution
of Bismarck brown was therefore injected under the skin of the back of
several frogs. After some hours the tissues became uniformly tinted a deep
yellow; the muscular substance especially had a very marked yellow tint.
The frogs did not appear in the least incommoded. Small fry of trout placed
in a solution stained rapidly and continued to swim about. Finally, a guinea-
pig, under whose skin some powder of Bismarck brown had been
introduced, soon presented a yellow staining of the buccal and anal mucous
membranes and of the skin. Seeds of cress sown on cotton soaked with a
concentrated solution of the Bismarck brown sprouted, and the young plants
were strongly stained brown; but on crushing the tissues and examining
them under the microscope, it was ascertained that the protoplasm of the
cells was very feebly coloured: the vessels, on the contrary, showed a deep
brown stain up to their termination of the leaf. The mycelium of a mould
developed in a solution of Bismarck brown was clearly stained after having
been washed in water, whilst it is known that the mycelium, which
frequently forms in coloured solutions, picro-carmine, hæmatoxylin, &c.,
remained perfectly colourless. Other aniline colours injected under the skin
of frogs stained the connective tissue as deeply as did the Bismarck brown;
but the striæ of muscle remained colourless. We may conclude, then, that
Bismarck brown possesses the quality of colouring living protoplasm both
in plants and in animals.
Cutting, Grinding, and Mounting Hard Structures.
Take the femur of cat, or rabbit, remove as much of the muscle as possible
and macerate it in water until quite clean; on removal hang it up to dry.
With a fine saw make transverse and longitudinal sections. File the section
down until flat, and smooth. Take some Canada balsam, place a piece on a
square of glass and warm gently over a lamp until the balsam is plastic
enough to allow of the section being pressed into it, and set it aside to
consolidate. Take a hone (“Water-of-Ayr” stone), moisten it with water, and
rub one side of the section upon it until quite smooth, then place the glass
slip, with the section still attached, into methylated spirit, and in a very
short time the section will be separated; wash it and remount it on the
the same way in the presence of aniline brown. A tolerably strong solution
of Bismarck brown was therefore injected under the skin of the back of
several frogs. After some hours the tissues became uniformly tinted a deep
yellow; the muscular substance especially had a very marked yellow tint.
The frogs did not appear in the least incommoded. Small fry of trout placed
in a solution stained rapidly and continued to swim about. Finally, a guinea-
pig, under whose skin some powder of Bismarck brown had been
introduced, soon presented a yellow staining of the buccal and anal mucous
membranes and of the skin. Seeds of cress sown on cotton soaked with a
concentrated solution of the Bismarck brown sprouted, and the young plants
were strongly stained brown; but on crushing the tissues and examining
them under the microscope, it was ascertained that the protoplasm of the
cells was very feebly coloured: the vessels, on the contrary, showed a deep
brown stain up to their termination of the leaf. The mycelium of a mould
developed in a solution of Bismarck brown was clearly stained after having
been washed in water, whilst it is known that the mycelium, which
frequently forms in coloured solutions, picro-carmine, hæmatoxylin, &c.,
remained perfectly colourless. Other aniline colours injected under the skin
of frogs stained the connective tissue as deeply as did the Bismarck brown;
but the striæ of muscle remained colourless. We may conclude, then, that
Bismarck brown possesses the quality of colouring living protoplasm both
in plants and in animals.
Cutting, Grinding, and Mounting Hard Structures.
Take the femur of cat, or rabbit, remove as much of the muscle as possible
and macerate it in water until quite clean; on removal hang it up to dry.
With a fine saw make transverse and longitudinal sections. File the section
down until flat, and smooth. Take some Canada balsam, place a piece on a
square of glass and warm gently over a lamp until the balsam is plastic
enough to allow of the section being pressed into it, and set it aside to
consolidate. Take a hone (“Water-of-Ayr” stone), moisten it with water, and
rub one side of the section upon it until quite smooth, then place the glass
slip, with the section still attached, into methylated spirit, and in a very
short time the section will be separated; wash it and remount it on the
Page 366
reverse side, and proceed to rub it down on the hone until it appears to be
thin enough for mounting. Polish both sides on a polishing strop with
Tripoli powder, and mount in Canada balsam.
thin enough for mounting. Polish both sides on a polishing strop with
Tripoli powder, and mount in Canada balsam.
Page 367
Teeth.—The enamel of the teeth
is a much harder structure than
that of bone, consequently it is
found necessary to have recourse
to a cutting machine. Hand
machines have been introduced
for this purpose, but the small
lathe described in the earlier
editions of my book has in no
way been superseded by later
cutting machines. Fig. 244
represents the small lathe used
for cutting and polishing every
kind of hard substance. With
regard to the teeth, two sections
should be made perpendicular to
one another through the middle
of the crown and fang of the
Fig. 244.—Small Lathe for cutting and polishing tooth from before backwards, and
Sections of Teeth. from right to left, which will
show the peculiar structure of the
enamel. The section must be cemented to the carrier of the stock of the
lathe, or to the metal plate a, and kept in position by the steel holder b; the
wheel being set in motion by the first treadle. The embedding materials in
use are either gum-shellac or Canada balsam. The former is more generally
employed by the lapidary and grinder of lenses than the latter. As the
enamel is liable to fracture under the saw, it will be necessary to lessen the
friction by dripping water on the saw as it is made to revolve. Thick
sections can be quickly ground down against the corrondum wheel. The
final polishing of the section may be done on the lathe, or by rubbing the
flattened surface with water upon a “Water-of-Ayr” stone, and ultimately set
up in Canada balsam, which must not be too fluid, or it will penetrate the
lacunæ and canaliculi, fill up the interspaces, and cause them to become
quite invisible. As the flatness of the polishing surfaces is a matter of
importance, the stones themselves should be tested from time to time, and
when found to present an uneven surface must be rubbed down on a granite
is a much harder structure than
that of bone, consequently it is
found necessary to have recourse
to a cutting machine. Hand
machines have been introduced
for this purpose, but the small
lathe described in the earlier
editions of my book has in no
way been superseded by later
cutting machines. Fig. 244
represents the small lathe used
for cutting and polishing every
kind of hard substance. With
regard to the teeth, two sections
should be made perpendicular to
one another through the middle
of the crown and fang of the
Fig. 244.—Small Lathe for cutting and polishing tooth from before backwards, and
Sections of Teeth. from right to left, which will
show the peculiar structure of the
enamel. The section must be cemented to the carrier of the stock of the
lathe, or to the metal plate a, and kept in position by the steel holder b; the
wheel being set in motion by the first treadle. The embedding materials in
use are either gum-shellac or Canada balsam. The former is more generally
employed by the lapidary and grinder of lenses than the latter. As the
enamel is liable to fracture under the saw, it will be necessary to lessen the
friction by dripping water on the saw as it is made to revolve. Thick
sections can be quickly ground down against the corrondum wheel. The
final polishing of the section may be done on the lathe, or by rubbing the
flattened surface with water upon a “Water-of-Ayr” stone, and ultimately set
up in Canada balsam, which must not be too fluid, or it will penetrate the
lacunæ and canaliculi, fill up the interspaces, and cause them to become
quite invisible. As the flatness of the polishing surfaces is a matter of
importance, the stones themselves should be tested from time to time, and
when found to present an uneven surface must be rubbed down on a granite
Page 368
stone with fine sand, or on a lead plate with emery powder. If it is decided
to use Canada balsam as the embedding material, this must be prepared in
the following manner:—The section of tooth or bone must be attached to a
slip of well-annealed glass by hardened Canada balsam, and its adhesion
effectually secured by placing the slide on the cover of a water bath, or in
the hot-chamber (Fig. 256), when the balsam, a thick drop of which should
be used, will spread out by liquefaction. The slide should then be removed
and allowed to cool in order that the hardness of the balsam may be tested.
If too soft, as indicated by its readily yielding to the pressure of the thumb-
nail, the heating process must be repeated, care being taken not to cause it
to boil and form bubbles; if too hard, which will be shown by its chipping,
it must be remelted and diluted with fluid balsam, and then set aside as
before. When it is found to be of the right consistence, the section must be
laid upon its surface with the polished side downwards; the slip of glass is
next to be gradually warmed until the balsam is softened, care being taken
to avoid the formation of bubbles, then press the section gently down with a
needle upon the liquefied balsam, the pressure being just applied on one
side rather than over the whole surface, so as to drive the superfluous
balsam towards the opposite side; finally, an equable pressure over the
whole will secure a perfect attachment of the section without air bubbles. If,
however, these should present themselves in drying, and they cannot
otherwise be expelled by pressure, it will be found better to take the section
off and relay it as before. The thickness of the layer of balsam may be
reduced by rubbing it down before applying the glass-cover.
Rock Sections.—Small pieces of rock may be ground down by the aid of the
lathe, or on a zinc plate, with emery powder and water, until one side is
rendered smooth and flat. Then fasten the polished side of the section to a
square of glass on the metal holder of the lathe, with dried Canada balsam,
as directed for bone, and allow it time to become consolidated. When
moderately thin take a piece of plate-glass and some fine emery or putty-
powder and rub the section down as thin as possible. When found to be thin
enough wash it well in water, and put it aside to dry, or warm it over a
spirit-lamp, and with a needle push the section off the glass into a watch-
glass of benzole or turpentine, and allow it to soak until all the balsam is
dissolved out. Wash again in turpentine, and mount in Canada balsam, with
or without a cover-glass. Sections of echinus spines, shells, stones of fruits,
to use Canada balsam as the embedding material, this must be prepared in
the following manner:—The section of tooth or bone must be attached to a
slip of well-annealed glass by hardened Canada balsam, and its adhesion
effectually secured by placing the slide on the cover of a water bath, or in
the hot-chamber (Fig. 256), when the balsam, a thick drop of which should
be used, will spread out by liquefaction. The slide should then be removed
and allowed to cool in order that the hardness of the balsam may be tested.
If too soft, as indicated by its readily yielding to the pressure of the thumb-
nail, the heating process must be repeated, care being taken not to cause it
to boil and form bubbles; if too hard, which will be shown by its chipping,
it must be remelted and diluted with fluid balsam, and then set aside as
before. When it is found to be of the right consistence, the section must be
laid upon its surface with the polished side downwards; the slip of glass is
next to be gradually warmed until the balsam is softened, care being taken
to avoid the formation of bubbles, then press the section gently down with a
needle upon the liquefied balsam, the pressure being just applied on one
side rather than over the whole surface, so as to drive the superfluous
balsam towards the opposite side; finally, an equable pressure over the
whole will secure a perfect attachment of the section without air bubbles. If,
however, these should present themselves in drying, and they cannot
otherwise be expelled by pressure, it will be found better to take the section
off and relay it as before. The thickness of the layer of balsam may be
reduced by rubbing it down before applying the glass-cover.
Rock Sections.—Small pieces of rock may be ground down by the aid of the
lathe, or on a zinc plate, with emery powder and water, until one side is
rendered smooth and flat. Then fasten the polished side of the section to a
square of glass on the metal holder of the lathe, with dried Canada balsam,
as directed for bone, and allow it time to become consolidated. When
moderately thin take a piece of plate-glass and some fine emery or putty-
powder and rub the section down as thin as possible. When found to be thin
enough wash it well in water, and put it aside to dry, or warm it over a
spirit-lamp, and with a needle push the section off the glass into a watch-
glass of benzole or turpentine, and allow it to soak until all the balsam is
dissolved out. Wash again in turpentine, and mount in Canada balsam, with
or without a cover-glass. Sections of echinus spines, shells, stones of fruits,
Page 369
&c., are prepared in the same way as those of bones and teeth; but when the
grinding is finished, the sections must be passed through alcohol into oil of
cloves, after which they should be mounted in Canada balsam. If tolerably
thin, sections of these substances can be cut in the lathe; in the first
instance, there will be no actual occasion to attach them to glass at all,
except for the purpose of obtaining a hold upon the specimen for polishing,
but the surface thus attached must afterwards be completely removed in
order to bring into view a stratum which the Canada balsam may not have
penetrated.
With regard to smaller bodies, these can scarcely be treated in any other
way than by attaching a number of them to slips of glass at once, and in
such a way as to make them mutually support each other. Thus in making
horizontal and vertical sections of foraminifera, it would be impossible to
slice them through unless they were laid close together in a bed of hardened
Canada balsam, and first grinding away one side and then turning and
rubbing down the other. My friend, Dr. Wallich, many years ago
communicated to me the ingenious plan adopted by himself when mounting
and turning a number of these minute objects together. The specimens being
cemented with Canada balsam, in the first instance, to a thin film of mica,
and then attached to a glass slide by the same means, when ground down to
the thinness desired, the slide must be gradually heated just sufficiently to
allow of the detachment of the mica-film and the specimen it carries; a
clean slide with a thin layer of hardened balsam having been prepared, the
mica-film is transferred to it with the ground surface downward. Its
adhesion by drying having been complete, the grinding and polishing
should be proceeded with; and as the mica-film will yield to the stone
without any difficulty, the specimen now reversed in position may be
further reduced to the requisite thickness for mounting as a permanent
object.
Staining and Mounting Vegetable Tissues.—Bacteria I propose to treat of in
a separate section. Vegetable tissues generally will first receive attention,
and their differentiation is based on the employment of delicate gradations
of colour stains. The more striking results are obtained by Multiple
Staining, while the cell contents are rendered more palpable. On this
account colouring media have been divided into nuclear, plasmic, and
grinding is finished, the sections must be passed through alcohol into oil of
cloves, after which they should be mounted in Canada balsam. If tolerably
thin, sections of these substances can be cut in the lathe; in the first
instance, there will be no actual occasion to attach them to glass at all,
except for the purpose of obtaining a hold upon the specimen for polishing,
but the surface thus attached must afterwards be completely removed in
order to bring into view a stratum which the Canada balsam may not have
penetrated.
With regard to smaller bodies, these can scarcely be treated in any other
way than by attaching a number of them to slips of glass at once, and in
such a way as to make them mutually support each other. Thus in making
horizontal and vertical sections of foraminifera, it would be impossible to
slice them through unless they were laid close together in a bed of hardened
Canada balsam, and first grinding away one side and then turning and
rubbing down the other. My friend, Dr. Wallich, many years ago
communicated to me the ingenious plan adopted by himself when mounting
and turning a number of these minute objects together. The specimens being
cemented with Canada balsam, in the first instance, to a thin film of mica,
and then attached to a glass slide by the same means, when ground down to
the thinness desired, the slide must be gradually heated just sufficiently to
allow of the detachment of the mica-film and the specimen it carries; a
clean slide with a thin layer of hardened balsam having been prepared, the
mica-film is transferred to it with the ground surface downward. Its
adhesion by drying having been complete, the grinding and polishing
should be proceeded with; and as the mica-film will yield to the stone
without any difficulty, the specimen now reversed in position may be
further reduced to the requisite thickness for mounting as a permanent
object.
Staining and Mounting Vegetable Tissues.—Bacteria I propose to treat of in
a separate section. Vegetable tissues generally will first receive attention,
and their differentiation is based on the employment of delicate gradations
of colour stains. The more striking results are obtained by Multiple
Staining, while the cell contents are rendered more palpable. On this
account colouring media have been divided into nuclear, plasmic, and
Page 370
specific. The first are chiefly valued in proportion as they prove to have a
selective affinity for the nuclei of cells, and leaving the protoplasm
comparatively unstained. Such stains are needful for fresh and young
tissues. On the other hand, plasmic stains colour tissue uniformly, and are
used to give a ground colour by way of contrast; and specific stains are
chiefly employed to distinguish certain elementary structures from the mass
of cellulose which forms the basis of vegetable tissue, and which is also met
with to a slight extent in animal membranes.
Cellulose, as it occurs in plant life, presents a variety of physical properties:
sometimes it is soft, as in young plants, and again quite dense in older
structures. This fact accounts for the varying results obtained when
cellulose is subjected to the action of staining fluids, and whether the
cellulose occurs in a nearly pure form, as in cotton fibre, or in the modified
form of lignine or woody-fibre. Stains which readily attack young tissue
have little or no effect upon it in its maturer form. It is of much importance,
then, in the staining of fibres, as well as sections for the microscope, that
the cellulose should take the stain uniformly.
The staining of tissues may be effected in four ways. First, when the stain
has sufficient affinity for the tissue to be retained by it without the
intervention of any outside agent. Second, when the stain and mordant are
mixed and applied to the tissue in one solution. These two are the simplest
and easiest methods of staining. Third, when the tissue is first immersed in
the staining liquid and then transferred to some other liquid which shall fix
the colour upon the tissue. Fourth, when the tissue is first impregnated with
the mordant, or fixing agent, and then immersed in the stain. The last
method is the one usually followed in commercial works, and it is to be
recommended in the staining of microscopical preparations which do not
readily take the stain.
Nuclear Stains.—As in both vegetable and animal sections it is generally
the nuclei which form the landmarks of the structure, so the most important
class of reagents which are used in any of the branches of microscopical
work are the “nuclear stains.” There are several of these stains, the most
important of which is the hæmatoxylin, and when proper solutions are used
the results are very satisfactory. Many formulæ have been given, but there
selective affinity for the nuclei of cells, and leaving the protoplasm
comparatively unstained. Such stains are needful for fresh and young
tissues. On the other hand, plasmic stains colour tissue uniformly, and are
used to give a ground colour by way of contrast; and specific stains are
chiefly employed to distinguish certain elementary structures from the mass
of cellulose which forms the basis of vegetable tissue, and which is also met
with to a slight extent in animal membranes.
Cellulose, as it occurs in plant life, presents a variety of physical properties:
sometimes it is soft, as in young plants, and again quite dense in older
structures. This fact accounts for the varying results obtained when
cellulose is subjected to the action of staining fluids, and whether the
cellulose occurs in a nearly pure form, as in cotton fibre, or in the modified
form of lignine or woody-fibre. Stains which readily attack young tissue
have little or no effect upon it in its maturer form. It is of much importance,
then, in the staining of fibres, as well as sections for the microscope, that
the cellulose should take the stain uniformly.
The staining of tissues may be effected in four ways. First, when the stain
has sufficient affinity for the tissue to be retained by it without the
intervention of any outside agent. Second, when the stain and mordant are
mixed and applied to the tissue in one solution. These two are the simplest
and easiest methods of staining. Third, when the tissue is first immersed in
the staining liquid and then transferred to some other liquid which shall fix
the colour upon the tissue. Fourth, when the tissue is first impregnated with
the mordant, or fixing agent, and then immersed in the stain. The last
method is the one usually followed in commercial works, and it is to be
recommended in the staining of microscopical preparations which do not
readily take the stain.
Nuclear Stains.—As in both vegetable and animal sections it is generally
the nuclei which form the landmarks of the structure, so the most important
class of reagents which are used in any of the branches of microscopical
work are the “nuclear stains.” There are several of these stains, the most
important of which is the hæmatoxylin, and when proper solutions are used
the results are very satisfactory. Many formulæ have been given, but there
Page 371
are three only reliable, Delafield’s, Kleinenberg’s, and Ehrlich’s, in all of
which alum is present as an ingredient; the idea being that the alumina
forms with the colouring matter an insoluble lake, and so acts as a mordant.
In Delafield’s solutions a large proportion of alum to hæmatoxylin is used,
and methylic alcohol (wood-spirit in the place of rectified spirit).
For Kleinenberg’s solution many different formulæ exist. Squire’s improved
formulæ for both stains is given in the Appendix, “Formulæ and Methods.”
Hæmatoxylin solutions stain the nuclei violet, and in order to change this
into blue, the sections should be transferred to water taken from the house
supply, not distilled water; but as the alkalinity of the water varies in
different localities, a better and more uniform result is obtained by using a
weak solution of bicarbonate of sodium (half a grain to the ounce).
Carmine is also much in vogue as a nuclear stain, and the two solutions
more generally employed are Greenacher’s alcoholic borax carmine, and
Orth’s lithium carmine. Under ordinary circumstances they act as general
stains, affecting the ground tissue as well as the nuclei. By subsequent
treatment with acidulated alcohol or acidulated glycerine the colour is
discharged from the ground tissue without seriously affecting the nuclei.
Used in this way, carmine becomes a good nuclear stain. It should be
remembered that the sections must not be washed in pure water, as the
colour will to a great extent be discharged; nor in acidulated water, as the
carmine will be precipitated.
Alum carmine and alum cochineal are useful nuclear stains, not requiring
after-treatment.
Picro-carmines are also largely used. The following formulæ will be found
the most useful:—
Ammonia Picro-carmine.—Carmine, one gramme; strong solution of
ammonia, three cc.; distilled water, five cc. Dissolve the carmine in the
ammonia and water with a gentle heat, then add saturated aqueous solution
of picric acid, 200 cc.; heat to boiling, and filter.
which alum is present as an ingredient; the idea being that the alumina
forms with the colouring matter an insoluble lake, and so acts as a mordant.
In Delafield’s solutions a large proportion of alum to hæmatoxylin is used,
and methylic alcohol (wood-spirit in the place of rectified spirit).
For Kleinenberg’s solution many different formulæ exist. Squire’s improved
formulæ for both stains is given in the Appendix, “Formulæ and Methods.”
Hæmatoxylin solutions stain the nuclei violet, and in order to change this
into blue, the sections should be transferred to water taken from the house
supply, not distilled water; but as the alkalinity of the water varies in
different localities, a better and more uniform result is obtained by using a
weak solution of bicarbonate of sodium (half a grain to the ounce).
Carmine is also much in vogue as a nuclear stain, and the two solutions
more generally employed are Greenacher’s alcoholic borax carmine, and
Orth’s lithium carmine. Under ordinary circumstances they act as general
stains, affecting the ground tissue as well as the nuclei. By subsequent
treatment with acidulated alcohol or acidulated glycerine the colour is
discharged from the ground tissue without seriously affecting the nuclei.
Used in this way, carmine becomes a good nuclear stain. It should be
remembered that the sections must not be washed in pure water, as the
colour will to a great extent be discharged; nor in acidulated water, as the
carmine will be precipitated.
Alum carmine and alum cochineal are useful nuclear stains, not requiring
after-treatment.
Picro-carmines are also largely used. The following formulæ will be found
the most useful:—
Ammonia Picro-carmine.—Carmine, one gramme; strong solution of
ammonia, three cc.; distilled water, five cc. Dissolve the carmine in the
ammonia and water with a gentle heat, then add saturated aqueous solution
of picric acid, 200 cc.; heat to boiling, and filter.
Page 372
Picro-Lithium Carmine.—The following is generally preferred for use—
Lithium carmine solution, 100 cc.; saturated solution of picric acid, 270 cc.
There are several aniline dyes which are used for nuclear staining:
methylene blue, methyl green, safranine, gentian violet, vesuvine, fuchsine,
and Hoffmann’s blue.
The usual process is to stain in ¼ or ½ per cent. aqueous solutions and wash
in methylated spirit. Methylene blue and methyl green have the reputation
of being so readily washed out in the methylated spirit as to be worthless.
This is obviated by washing the sections (when removed from the stain) in
distilled water, previous to the differentiation in methylated spirit. Treated
in this manner, the nuclear staining is very beautiful. This also applies to
Hoffmann’s blue and partly to vesuvine; with the latter, however, it is not a
necessity. Safranine and gentian violet worked better by transferring the
sections directly from the stain into 90 per cent. alcohol.
Contrast Stains.—Very frequently other stains are used to dye the ground a
colour which is in contrast to that employed for the nuclei. Brown, orange,
or pink are used after nuclear blue or green. Carmine is generally
counterstained yellow or indigo-blue; and fuchsine red, as in tubercle
bacilli, is counterstained with nuclear blue. It is important that the ground
stain should be made weaker than the principal stain, so that the whole
tissue may be shown without detracting from the nuclei. The following
colours are used as counterstains for animal sections, but they prove less
useful for vegetable sections: benzo-purpurine, eosin, erythrosine, orange,
acid rubin, and picric acid.
Examples of specific stains are fuchsine, methylene blue, and gentian violet
for bacteria; osmic acid for fatty elements; victoria blue and rose bengale,
for demonstrating elastic tissue; methyl violet, iodine, and safranine, for
amyloid degeneration. Methylene blue is one of the most useful of aniline
dyes, and one of the most variable in composition.
Iodine green, or methyl green, has long been in use as a reagent for
amyloid, starchy matters, in ignorance of the fact that the reaction is due to
the methyl violet, contained as an impurity in the iodine green. It is
exceedingly difficult to obtain a green quite free from violet. As nuclear
Lithium carmine solution, 100 cc.; saturated solution of picric acid, 270 cc.
There are several aniline dyes which are used for nuclear staining:
methylene blue, methyl green, safranine, gentian violet, vesuvine, fuchsine,
and Hoffmann’s blue.
The usual process is to stain in ¼ or ½ per cent. aqueous solutions and wash
in methylated spirit. Methylene blue and methyl green have the reputation
of being so readily washed out in the methylated spirit as to be worthless.
This is obviated by washing the sections (when removed from the stain) in
distilled water, previous to the differentiation in methylated spirit. Treated
in this manner, the nuclear staining is very beautiful. This also applies to
Hoffmann’s blue and partly to vesuvine; with the latter, however, it is not a
necessity. Safranine and gentian violet worked better by transferring the
sections directly from the stain into 90 per cent. alcohol.
Contrast Stains.—Very frequently other stains are used to dye the ground a
colour which is in contrast to that employed for the nuclei. Brown, orange,
or pink are used after nuclear blue or green. Carmine is generally
counterstained yellow or indigo-blue; and fuchsine red, as in tubercle
bacilli, is counterstained with nuclear blue. It is important that the ground
stain should be made weaker than the principal stain, so that the whole
tissue may be shown without detracting from the nuclei. The following
colours are used as counterstains for animal sections, but they prove less
useful for vegetable sections: benzo-purpurine, eosin, erythrosine, orange,
acid rubin, and picric acid.
Examples of specific stains are fuchsine, methylene blue, and gentian violet
for bacteria; osmic acid for fatty elements; victoria blue and rose bengale,
for demonstrating elastic tissue; methyl violet, iodine, and safranine, for
amyloid degeneration. Methylene blue is one of the most useful of aniline
dyes, and one of the most variable in composition.
Iodine green, or methyl green, has long been in use as a reagent for
amyloid, starchy matters, in ignorance of the fact that the reaction is due to
the methyl violet, contained as an impurity in the iodine green. It is
exceedingly difficult to obtain a green quite free from violet. As nuclear
Page 373
stains they are identical, and the amyloid reaction, being dependent wholly
upon the contained violet, varies, not with the formula of the green, but
with the extent to which it has been purified.
Cellulose reactions.—After the nuclear stains, the most important reagents
to the botanist are those which affect cellulose and its several modifications.
Pure cellulose is coloured yellow by iodine, the colour being changed to a
blue on the addition of slightly dilute sulphuric acid, or a strong solution of
zinc. Solutions containing iodine, iodide of potassium, and chloride of zinc,
give a violet reaction with unaltered cellulose, and yellow with lignine.
Schulze’s zinc re-agent must be used with a certain amount of caution, as
the chloride of zinc and potassium undergo decomposition. The formula
now in use is as follows: Take of zinc chloride solution (sp. gr. 1·85) 70 cc.,
potassium iodide 10 grammes, iodine 0·1 gramme; but this solution can
only be employed as a re-agent and not as a dye, and structures stained with
it cannot be mounted in any of the ordinary media, and the only fluid for
ringing them down is caoutchouc cement.
Cellulose can be stained permanently by carmine, hæmatoxylin, nigrosine,
methylene blue, safranine, and fuchsine. The aniline dyes are used in dilute
aqueous solutions containing one-eighth or one-fourth per cent. of dye.
When the cellulose undergoes the change known as lignification its
reactions are altered. It is coloured yellow by chloro-zinc iodine, red by
phloroglucin, yellow by aniline chloride. The two latter are much assisted
by hydrochloric acid. The results of these reactions also cannot be preserved
in the usual mounting media.
Sections containing mixed tissue, partly unaltered cellulose and partly
lignified, give striking results with aniline dyes, and with this additional
advantage can be preserved for years.
Double Staining.—When a section is passed through methyl green solution
and afterwards one of carmine, the lignified portion is coloured green and
the unlignified red. Acid green may be used in the place of methyl green,
with a similar result. When picric acid is used with carmine, ingrosine, or
Hoffmann’s blue, the picric acid dyes the ligneous portion and the others
colour the unlignified structure, red, black, and blue respectively.
upon the contained violet, varies, not with the formula of the green, but
with the extent to which it has been purified.
Cellulose reactions.—After the nuclear stains, the most important reagents
to the botanist are those which affect cellulose and its several modifications.
Pure cellulose is coloured yellow by iodine, the colour being changed to a
blue on the addition of slightly dilute sulphuric acid, or a strong solution of
zinc. Solutions containing iodine, iodide of potassium, and chloride of zinc,
give a violet reaction with unaltered cellulose, and yellow with lignine.
Schulze’s zinc re-agent must be used with a certain amount of caution, as
the chloride of zinc and potassium undergo decomposition. The formula
now in use is as follows: Take of zinc chloride solution (sp. gr. 1·85) 70 cc.,
potassium iodide 10 grammes, iodine 0·1 gramme; but this solution can
only be employed as a re-agent and not as a dye, and structures stained with
it cannot be mounted in any of the ordinary media, and the only fluid for
ringing them down is caoutchouc cement.
Cellulose can be stained permanently by carmine, hæmatoxylin, nigrosine,
methylene blue, safranine, and fuchsine. The aniline dyes are used in dilute
aqueous solutions containing one-eighth or one-fourth per cent. of dye.
When the cellulose undergoes the change known as lignification its
reactions are altered. It is coloured yellow by chloro-zinc iodine, red by
phloroglucin, yellow by aniline chloride. The two latter are much assisted
by hydrochloric acid. The results of these reactions also cannot be preserved
in the usual mounting media.
Sections containing mixed tissue, partly unaltered cellulose and partly
lignified, give striking results with aniline dyes, and with this additional
advantage can be preserved for years.
Double Staining.—When a section is passed through methyl green solution
and afterwards one of carmine, the lignified portion is coloured green and
the unlignified red. Acid green may be used in the place of methyl green,
with a similar result. When picric acid is used with carmine, ingrosine, or
Hoffmann’s blue, the picric acid dyes the ligneous portion and the others
colour the unlignified structure, red, black, and blue respectively.
Page 374
Eosin stain is the most useful for sieve-tubes and plates. Make a strong
solution of eosin in equal parts of water and alcohol, and stain the section
for five or ten minutes. Wash well in methylated spirit, dehydrate, clean in
oil of cloves, and mount in Canada balsam.
Bleaching Process.—The bleaching and clearing of vegetable structures
before staining is a very necessary process, especially so if starch be present
in any quantity. Clearing agents are of two kinds—those which act by virtue
of their property of strongly refracting light, and those which disintegrate
and dissolve the amyloid cell contents. To the first class belong the essential
oils, as oil of cloves, Canada balsam, glycerine, and other similar bodies; to
the second class, solutions of potash, phenol, and chloral hydrate. The
actual value of some of these agents is questionable. The process usually
preferred is as follows: Place the sections in a fresh clear solution of
chlorinated lime, allowing them to remain until quite bleached, say from
two to four or five minutes; then gently warm in a test-tube for a few
seconds, and quickly replace the solution with distilled water and boil for
two or three minutes; repeat the treatment with boiling water three times;
wash with a one per cent. solution of acetic acid, and finally with distilled
water. The sections are then quite ready for staining operations.
When the stem is hard and brown, a solution of chloride of lime should be
used—a quarter of an ounce of chloride dissolved in a pint of water, well
shaken and stood by to settle down, then pour off the clear fluid for use. For
hard tissues this solution answers well, but it is not suitable for leaves, as
they require not only bleaching, but the cell contents should be dissolved
out to render them transparent. A solution of chlorinated soda answers well
for both stems and leaves. It is prepared as follows:—
To one pint of water add two ounces of fresh chloride of lime, shake or stir
it well two or three times, then allow it to stand till the lime has settled.
Prepare meanwhile a saturated solution of carbonate of soda—common
washing soda. Now pour off the clear supernatant fluid from the chloride of
lime, and add to it, by degrees, the soda solution, when a precipitate of
carbonate of lime will be thrown down; continue to add the soda solution
till no further precipitate is formed. Filter the solution, and keep it in a well-
stoppered bottle in the dark, otherwise it speedily spoils.
solution of eosin in equal parts of water and alcohol, and stain the section
for five or ten minutes. Wash well in methylated spirit, dehydrate, clean in
oil of cloves, and mount in Canada balsam.
Bleaching Process.—The bleaching and clearing of vegetable structures
before staining is a very necessary process, especially so if starch be present
in any quantity. Clearing agents are of two kinds—those which act by virtue
of their property of strongly refracting light, and those which disintegrate
and dissolve the amyloid cell contents. To the first class belong the essential
oils, as oil of cloves, Canada balsam, glycerine, and other similar bodies; to
the second class, solutions of potash, phenol, and chloral hydrate. The
actual value of some of these agents is questionable. The process usually
preferred is as follows: Place the sections in a fresh clear solution of
chlorinated lime, allowing them to remain until quite bleached, say from
two to four or five minutes; then gently warm in a test-tube for a few
seconds, and quickly replace the solution with distilled water and boil for
two or three minutes; repeat the treatment with boiling water three times;
wash with a one per cent. solution of acetic acid, and finally with distilled
water. The sections are then quite ready for staining operations.
When the stem is hard and brown, a solution of chloride of lime should be
used—a quarter of an ounce of chloride dissolved in a pint of water, well
shaken and stood by to settle down, then pour off the clear fluid for use. For
hard tissues this solution answers well, but it is not suitable for leaves, as
they require not only bleaching, but the cell contents should be dissolved
out to render them transparent. A solution of chlorinated soda answers well
for both stems and leaves. It is prepared as follows:—
To one pint of water add two ounces of fresh chloride of lime, shake or stir
it well two or three times, then allow it to stand till the lime has settled.
Prepare meanwhile a saturated solution of carbonate of soda—common
washing soda. Now pour off the clear supernatant fluid from the chloride of
lime, and add to it, by degrees, the soda solution, when a precipitate of
carbonate of lime will be thrown down; continue to add the soda solution
till no further precipitate is formed. Filter the solution, and keep it in a well-
stoppered bottle in the dark, otherwise it speedily spoils.
Page 375
Sections bleached in chlorinated soda must, when white enough, be washed
in distilled water, and allowed to remain in it for twenty-four hours,
changing the water four or five times, and adding a few drops of nitric acid,
or at the rate of eight or ten drops to the half-pint, to the water employed
before the final washing takes place. From water transfer them to alcohol,
in which they must remain for an hour or more.
Although alkaline glycerine has been recommended for several purposes in
micro-technique, it is not so well known as it should be how serviceable it
is as an extempore mounting solution in vegetable histology. The best
mixture for general use is composed of glycerine 2 ozs., distilled water 1½
oz., solution of potash, B.P., ½ oz. This combines the refringent property of
the glycerine with the clearing action of the caustic potash, while the
swelling action of the potash is considerably diminished.
Cutting Sections of Hard Woods.—The lathe and circular saw will be found
as useful for cutting sections of the harder kinds of woods, as for bone
structure. It may be necessary to subject the older and consequently harder
pieces of wood to the action of steam for a few hours to soften them, and
afterwards transfer them to methylated spirit, before making an attempt to
cut sections. But the more open woods, of one, two, or three years’ growth,
will show all that may be required, and these can be cut by hand, or with the
microtome, as already described.
With a little practice the finest and thinnest possible slices may be cut by
hand. It is usual to take off the first slice to give a smooth and even surface
to the specimen. Then turn the screw to raise it a little, sprinkle the surface
with spirit and water, and cut with a light hand. Remove the cut sections
with a fine camel’s-hair brush or a section lifter (Fig. 250) to a small vessel
containing water, when the thinnest will float on the surface, and remove to
methylated spirit and water, where they should remain until they can be
mounted. Sections of hard woods, and those containing gum-resins, or other
insoluble material, must first be kept in methylated spirit or alcohol, and
finally transferred to oil of cloves, to render them sufficiently transparent
for mounting in Canada balsam.
If the structure of an exogenous wood is required to be examined, the
sections should be made in at least three different ways: the transverse, the
in distilled water, and allowed to remain in it for twenty-four hours,
changing the water four or five times, and adding a few drops of nitric acid,
or at the rate of eight or ten drops to the half-pint, to the water employed
before the final washing takes place. From water transfer them to alcohol,
in which they must remain for an hour or more.
Although alkaline glycerine has been recommended for several purposes in
micro-technique, it is not so well known as it should be how serviceable it
is as an extempore mounting solution in vegetable histology. The best
mixture for general use is composed of glycerine 2 ozs., distilled water 1½
oz., solution of potash, B.P., ½ oz. This combines the refringent property of
the glycerine with the clearing action of the caustic potash, while the
swelling action of the potash is considerably diminished.
Cutting Sections of Hard Woods.—The lathe and circular saw will be found
as useful for cutting sections of the harder kinds of woods, as for bone
structure. It may be necessary to subject the older and consequently harder
pieces of wood to the action of steam for a few hours to soften them, and
afterwards transfer them to methylated spirit, before making an attempt to
cut sections. But the more open woods, of one, two, or three years’ growth,
will show all that may be required, and these can be cut by hand, or with the
microtome, as already described.
With a little practice the finest and thinnest possible slices may be cut by
hand. It is usual to take off the first slice to give a smooth and even surface
to the specimen. Then turn the screw to raise it a little, sprinkle the surface
with spirit and water, and cut with a light hand. Remove the cut sections
with a fine camel’s-hair brush or a section lifter (Fig. 250) to a small vessel
containing water, when the thinnest will float on the surface, and remove to
methylated spirit and water, where they should remain until they can be
mounted. Sections of hard woods, and those containing gum-resins, or other
insoluble material, must first be kept in methylated spirit or alcohol, and
finally transferred to oil of cloves, to render them sufficiently transparent
for mounting in Canada balsam.
If the structure of an exogenous wood is required to be examined, the
sections should be made in at least three different ways: the transverse, the
Page 376
longitudinal, and the oblique, or, as they are sometimes called, the
horizontal, vertical, and tangential, each of which will exhibit different
appearances, as seen in Fig. 245: b is a vertical section through the pith of a
coniferous plant, and exhibits the medullary rays known to the cabinet-
maker as the silver grain; e is a magnified view of a part of the same; the
woody fibres are seen with their dots l, and the horizontal lines k indicating
the medullary rays cut lengthwise; c is a tangential section, and f a portion
of the same; the medullary rays m m, and the woody fibres with vertical
slices of the dots, are shown. Instructive preparations will be secured by
cutting oblique sections of the stem. The sections seen are made from the
pine. All exogenous stems, however, exhibit three different appearances,
according to the direction in which the section is made.
Fig. 245.—Sections of Wood.
Bacteria Cultivation, Sterilising, and Preparing for Microscopical
Examination.
horizontal, vertical, and tangential, each of which will exhibit different
appearances, as seen in Fig. 245: b is a vertical section through the pith of a
coniferous plant, and exhibits the medullary rays known to the cabinet-
maker as the silver grain; e is a magnified view of a part of the same; the
woody fibres are seen with their dots l, and the horizontal lines k indicating
the medullary rays cut lengthwise; c is a tangential section, and f a portion
of the same; the medullary rays m m, and the woody fibres with vertical
slices of the dots, are shown. Instructive preparations will be secured by
cutting oblique sections of the stem. The sections seen are made from the
pine. All exogenous stems, however, exhibit three different appearances,
according to the direction in which the section is made.
Fig. 245.—Sections of Wood.
Bacteria Cultivation, Sterilising, and Preparing for Microscopical
Examination.
Page 377
That branch of mycology which is now looked upon as a separate
department of science, termed bacteriology, took shape in the years 1875-9,
when its founder, the veteran botanist Cohn, who recognised that the
protoplasm of plants corresponded to the animal sarcode, published his
exact mode of studying bacteria. But it was a pupil of his, Dr. Koch, who a
year later discovered that a specific cattle disease, anthrax, was due to a
bacillus, and it was he also who gave us the useful modification of gelatine
as a medium in which to grow bacteria; he hit upon the method of pouring
melted gelatine containing distributed germs on to plates, and thus isolating
the colonies and ensuring the further isolation of the spores, and so facilitate
the preparation of pure cultures on a large scale, and with great saving of
time.
The difficulty of isolating a bacterium and tracing its life history under the
microscope must at first sight appear great. A further objection that such
work is slow and difficult has no more weight here than in any other
department of science, as will be seen on proceeding to follow out the
directions I am about to furnish for the use of the student.
Apparatus, Material, and Reagents employed in Bacteriological
Investigations.
A good microscope with a wide-angled sub-stage condenser, and objectives
of an inch, ¼-inch, or 1⁄6-inch, and a 1⁄12-inch homogeneous oil-immersion.
A large bell-glass for covering the same when fuming acids are in use in the
laboratory.
About a square foot of blackened plate-glass.
A white porcelain slab, or a shallow photographic dish of some size.
Glass bottles with ground stoppers for alcoholic solutions and aniline dyes.
Glass bottles with funnels for filtering solutions of stains, with pipettes.
department of science, termed bacteriology, took shape in the years 1875-9,
when its founder, the veteran botanist Cohn, who recognised that the
protoplasm of plants corresponded to the animal sarcode, published his
exact mode of studying bacteria. But it was a pupil of his, Dr. Koch, who a
year later discovered that a specific cattle disease, anthrax, was due to a
bacillus, and it was he also who gave us the useful modification of gelatine
as a medium in which to grow bacteria; he hit upon the method of pouring
melted gelatine containing distributed germs on to plates, and thus isolating
the colonies and ensuring the further isolation of the spores, and so facilitate
the preparation of pure cultures on a large scale, and with great saving of
time.
The difficulty of isolating a bacterium and tracing its life history under the
microscope must at first sight appear great. A further objection that such
work is slow and difficult has no more weight here than in any other
department of science, as will be seen on proceeding to follow out the
directions I am about to furnish for the use of the student.
Apparatus, Material, and Reagents employed in Bacteriological
Investigations.
A good microscope with a wide-angled sub-stage condenser, and objectives
of an inch, ¼-inch, or 1⁄6-inch, and a 1⁄12-inch homogeneous oil-immersion.
A large bell-glass for covering the same when fuming acids are in use in the
laboratory.
About a square foot of blackened plate-glass.
A white porcelain slab, or a shallow photographic dish of some size.
Glass bottles with ground stoppers for alcoholic solutions and aniline dyes.
Glass bottles with funnels for filtering solutions of stains, with pipettes.
Page 378
A specialised form of pipette for the micro-chemical filtration of solutions
(Fig. 246).
A small stoppered bottle of cedar oil (Fig. 247).
Set of small glass dishes or watch-glasses for section staining.
Stock of glass slides sterilised, together with round thin glass-covers, in
boxes (Fig. 248).
Needle holders and platinum needles, with a packet of ordinary sewing
needles (Fig. 249).
Platinum, or plated copper section-lifters (Fig. 250).
Glass rods, drawn out to a fine point, for manipulating sections when acids
are employed.
(Fig. 246).
A small stoppered bottle of cedar oil (Fig. 247).
Set of small glass dishes or watch-glasses for section staining.
Stock of glass slides sterilised, together with round thin glass-covers, in
boxes (Fig. 248).
Needle holders and platinum needles, with a packet of ordinary sewing
needles (Fig. 249).
Platinum, or plated copper section-lifters (Fig. 250).
Glass rods, drawn out to a fine point, for manipulating sections when acids
are employed.
Page 379
Fig. 247.—Bottle
and Dipper for
Cedar Oil.
Fig. 248.—Box Fig. 249.—Needle Holders,
Fig. 246.—Pipette for keeping Glass- fine Lifter and Hook for
for Micro-chemical covers. Manipulating Structure.
Filtration.
and Dipper for
Cedar Oil.
Fig. 248.—Box Fig. 249.—Needle Holders,
Fig. 246.—Pipette for keeping Glass- fine Lifter and Hook for
for Micro-chemical covers. Manipulating Structure.
Filtration.
Page 380
Fig. 250.—Section
Lifters.
Fig. 251a.—Forceps with fine
Fig. 251.—Spring Points.
Flat Forceps.
A pair of small spring steel platinum-pointed forceps for holding glass-
covers (Fig. 251).
One or two pairs of fine-pointed forceps (Fig. 251a).
Collapsible tubes for containing Canada balsam and dammar.
Soft rags or old pocket handkerchiefs for removing cedar oil from lenses
and cover-glasses. Chamois leather for wiping lenses and removing dust.
Reagents, alcohol, bergamot oil, celloidin, dissolved in equal parts of ether
and alcohol.
Lifters.
Fig. 251a.—Forceps with fine
Fig. 251.—Spring Points.
Flat Forceps.
A pair of small spring steel platinum-pointed forceps for holding glass-
covers (Fig. 251).
One or two pairs of fine-pointed forceps (Fig. 251a).
Collapsible tubes for containing Canada balsam and dammar.
Soft rags or old pocket handkerchiefs for removing cedar oil from lenses
and cover-glasses. Chamois leather for wiping lenses and removing dust.
Reagents, alcohol, bergamot oil, celloidin, dissolved in equal parts of ether
and alcohol.
Page 381
Ebner’s solution. (See Appendix.)
Formalin, glycerine, gelatine, Klebs’ and Kleinenberg’s solutions. (See
Appendix.) The latter consisting of a watery solution of picric acid 100
parts; strong sulphuric acid two parts; filter, and add distilled water 300
parts.
Muller fluid. (See Appendix.)
Osmic acid, a five per cent. solution.
Paraffin, spermaceti and xylol, acetic acid, hydrochloric acid, a one per
cent. solution with alcohol.
Ammonia liquid, ether, picro-lithium carmine, potash solution.
Safranine, concentrated alcoholic solution of, and a watery solution.
Turpentine, vesuvin, water distilled and sterilised.
Aqueous solutions of the several dyes may be kept in bottles ready for use.
To both aqueous and alcoholic solutions a few drops of phenol, or a crystal
of thymol, should be added as a preservative. For the rapid staining of
cover-glass preparations, it is convenient to have the most frequently used
stains—fuchsine, methyl-violet, &c.—in bottles provided with pipette
stoppers.
Clearing Agents.—Oils of cedar wood, cloves, origanum, aniline, terebene,
toluol and xylol, benzol and spirits of turpentine.
Mounting Media.—Acetate of potash solution concentrated, benzole,
balsam, glycerine jelly, Fanant’s medium, dammar and mastic, Canada
balsam in xylol, Hollis’s glue, zinc white.
Cement for fixing small specimens temporarily to a glass slide. Remove all
traces of moisture, place upon it a drop or two of a medium prepared as
follows:—Dissolve over a water bath 15 grammes of white lac in 100
Formalin, glycerine, gelatine, Klebs’ and Kleinenberg’s solutions. (See
Appendix.) The latter consisting of a watery solution of picric acid 100
parts; strong sulphuric acid two parts; filter, and add distilled water 300
parts.
Muller fluid. (See Appendix.)
Osmic acid, a five per cent. solution.
Paraffin, spermaceti and xylol, acetic acid, hydrochloric acid, a one per
cent. solution with alcohol.
Ammonia liquid, ether, picro-lithium carmine, potash solution.
Safranine, concentrated alcoholic solution of, and a watery solution.
Turpentine, vesuvin, water distilled and sterilised.
Aqueous solutions of the several dyes may be kept in bottles ready for use.
To both aqueous and alcoholic solutions a few drops of phenol, or a crystal
of thymol, should be added as a preservative. For the rapid staining of
cover-glass preparations, it is convenient to have the most frequently used
stains—fuchsine, methyl-violet, &c.—in bottles provided with pipette
stoppers.
Clearing Agents.—Oils of cedar wood, cloves, origanum, aniline, terebene,
toluol and xylol, benzol and spirits of turpentine.
Mounting Media.—Acetate of potash solution concentrated, benzole,
balsam, glycerine jelly, Fanant’s medium, dammar and mastic, Canada
balsam in xylol, Hollis’s glue, zinc white.
Cement for fixing small specimens temporarily to a glass slide. Remove all
traces of moisture, place upon it a drop or two of a medium prepared as
follows:—Dissolve over a water bath 15 grammes of white lac in 100
Page 382
grammes of absolute alcohol, decant off the clear liquid, and stand it by for
a while.
As the alcohol evaporates from the warmed surface of the glass slide a hard
transparent coating is left. This may be slightly softened at any time by
means of a drop of oil of lavender. After arranging the objects the heat of a
spirit-lamp will cause the oil to evaporate, leaving them firmly attached.
Objects may be mounted on cover-glasses in a similar way. A resinous
mounting medium may then be employed in the usual manner. If glycerine
or glycerine jelly is the mounting medium employed, collodion diluted with
two or three times its volume of oil of lavender may be found preferable as
the fixing agent. The section should be placed in position before the
preparation dries and the oil is evaporated.
Methylated spirit is often so largely adulterated with rock-oil as to render it
unsuitable for technical purposes. Even to varnishes it imparts a fluorescent
appearance as it dries off.
Fig. 252.—Iron Box for holding Sterilised Instruments and Glass Plates.
The needles and instruments used must not be passed through a Bunsen
burner flame, which is most destructive, but enclosed in a sheet-iron box
made for the purpose (Fig. 252), and placed in the hot-air steriliser for an
hour at 150°C. The box can be opened at the side, and each instrument
withdrawn with a pair of sterilised forceps when required for use.
Glass plates are sterilised in the same iron box, and the platinum needles
for inoculating nutrient media, examining cultivations, &c., are served in
the same manner before being used. The needles consist of two or three
inches of platinum wire fixed to the end of a glass rod. Several of these
needles should be made by fixing pieces of wire into a glass rod about six
a while.
As the alcohol evaporates from the warmed surface of the glass slide a hard
transparent coating is left. This may be slightly softened at any time by
means of a drop of oil of lavender. After arranging the objects the heat of a
spirit-lamp will cause the oil to evaporate, leaving them firmly attached.
Objects may be mounted on cover-glasses in a similar way. A resinous
mounting medium may then be employed in the usual manner. If glycerine
or glycerine jelly is the mounting medium employed, collodion diluted with
two or three times its volume of oil of lavender may be found preferable as
the fixing agent. The section should be placed in position before the
preparation dries and the oil is evaporated.
Methylated spirit is often so largely adulterated with rock-oil as to render it
unsuitable for technical purposes. Even to varnishes it imparts a fluorescent
appearance as it dries off.
Fig. 252.—Iron Box for holding Sterilised Instruments and Glass Plates.
The needles and instruments used must not be passed through a Bunsen
burner flame, which is most destructive, but enclosed in a sheet-iron box
made for the purpose (Fig. 252), and placed in the hot-air steriliser for an
hour at 150°C. The box can be opened at the side, and each instrument
withdrawn with a pair of sterilised forceps when required for use.
Glass plates are sterilised in the same iron box, and the platinum needles
for inoculating nutrient media, examining cultivations, &c., are served in
the same manner before being used. The needles consist of two or three
inches of platinum wire fixed to the end of a glass rod. Several of these
needles should be made by fixing pieces of wire into a glass rod about six
Page 383
inches long. The glass rod must be heated at the extreme end in the flame of
a Bunsen burner, or blow-pipe, and the platinum wire held near one
extremity with forceps, and fused into the end of the glass rod. Some of
these rods should be straight, and some bent, and others provided with a
loop, and kept especially ready for inoculating test-tubes of nutrient jelly.
Fig. 253.—Damp Chamber for Plate-cultivations.
Glass Dishes.—Several shallow glass dishes are required for preparing
damp chamber cultivations, the upper covers fitting over the under (as in
Fig. 253), in the centre of which culture-plates are stacked one above the
other, and when necessary placed in the incubator.
Apparatus for Incubation and Cultivations in Liquid Media.
Lister’s Flasks.—Lister devised a globe-shaped flask with two necks, a
vertical and a lateral one, the lateral being a bent spout, tapering towards the
extremity. When the vessel is restored to the erect position after pouring out
some of its contents, a drop of liquid remains behind in the end of the
nozzle, and thus prevents the regurgitation of air through the spout. A cap of
cotton-wool is tied over the orifice, and the residue left in the flask for
future use. The vertical neck of the flask is plugged with sterilised cotton-
wool in the ordinary way.
a Bunsen burner, or blow-pipe, and the platinum wire held near one
extremity with forceps, and fused into the end of the glass rod. Some of
these rods should be straight, and some bent, and others provided with a
loop, and kept especially ready for inoculating test-tubes of nutrient jelly.
Fig. 253.—Damp Chamber for Plate-cultivations.
Glass Dishes.—Several shallow glass dishes are required for preparing
damp chamber cultivations, the upper covers fitting over the under (as in
Fig. 253), in the centre of which culture-plates are stacked one above the
other, and when necessary placed in the incubator.
Apparatus for Incubation and Cultivations in Liquid Media.
Lister’s Flasks.—Lister devised a globe-shaped flask with two necks, a
vertical and a lateral one, the lateral being a bent spout, tapering towards the
extremity. When the vessel is restored to the erect position after pouring out
some of its contents, a drop of liquid remains behind in the end of the
nozzle, and thus prevents the regurgitation of air through the spout. A cap of
cotton-wool is tied over the orifice, and the residue left in the flask for
future use. The vertical neck of the flask is plugged with sterilised cotton-
wool in the ordinary way.
Page 384
Fig. 255.—Storing Cultivation
Fig. 254.—Pasteur’s Bulb Pipette. Tube.
Sternberg advocates the use of a glass bulb, provided with a slender neck
drawn out to a fine point and hermetically sealed. Special forms of tubes,
bulbs, and pipettes were devised by Pasteur, and are still in use at the
Bacteriological Institute, Paris, and known as the Pasteur’s bulb pipette
(Fig. 254).
Others are provided with lateral or with curved arms, one of which is drawn
out to a fine point, and the slender neck plugged with cotton-wool, as in
Fig. 255.
THE WARM CHAMBER, STERILISER, AND INCUBATOR.
Fig. 254.—Pasteur’s Bulb Pipette. Tube.
Sternberg advocates the use of a glass bulb, provided with a slender neck
drawn out to a fine point and hermetically sealed. Special forms of tubes,
bulbs, and pipettes were devised by Pasteur, and are still in use at the
Bacteriological Institute, Paris, and known as the Pasteur’s bulb pipette
(Fig. 254).
Others are provided with lateral or with curved arms, one of which is drawn
out to a fine point, and the slender neck plugged with cotton-wool, as in
Fig. 255.
THE WARM CHAMBER, STERILISER, AND INCUBATOR.
Page 385
Fig. 256.—Pfeiffer’s Warm Chamber.
The Warm Chamber.—This is an accessory of importance in bacteriological
work. For the continuous heating of specimens during cultivation it is an
absolute necessity. Pfeiffer’s warm chamber (Fig. 256) is suitable for
microscopical work generally. It consists of a hard-wood box, made air-
tight, with doors and glass windows to allow of the specimen being moved
from time to time, and kept under constant observation. The box is mounted
on a metal plate tripod stand, and is heated from below by a small gas
burner, with a thermo-regulator. A paraffin lamp will do as well, so long as
it maintains a temperature of from 25° to 45°C., and without danger of
injury to the stand and lenses of the microscope. A thermometer is placed in
the air space to mark the temperature.
The Warm Chamber.—This is an accessory of importance in bacteriological
work. For the continuous heating of specimens during cultivation it is an
absolute necessity. Pfeiffer’s warm chamber (Fig. 256) is suitable for
microscopical work generally. It consists of a hard-wood box, made air-
tight, with doors and glass windows to allow of the specimen being moved
from time to time, and kept under constant observation. The box is mounted
on a metal plate tripod stand, and is heated from below by a small gas
burner, with a thermo-regulator. A paraffin lamp will do as well, so long as
it maintains a temperature of from 25° to 45°C., and without danger of
injury to the stand and lenses of the microscope. A thermometer is placed in
the air space to mark the temperature.
Page 386
Fig. 257.—Crookshank’s Incubator.
Hot-air Incubators and Sterilisers are usually made of sheet-iron, in the
form of a cubical chest, with double walls, supported on four legs, as that of
Dr. Crookshank’s (Fig. 257). They are heated by gas or a lamp from below,
while the temperature is indicated by a thermometer inserted through a hole
in the top, as in that of the Hearson’s incubator. Test-tubes, flasks, funnels,
cotton-wool, &c., must be sterilised by exposure to a temperature of 150°C.
for an hour or more.
Wire Cages or crates are used for containing test-tubes, especially when
they are to be sterilised in the hot-air steriliser, or for lowering tubes of
nutrient jelly into the steam steriliser. All instruments, needles, scalpels,
&c., before using must be carefully sterilised.
Hot-air Incubators and Sterilisers are usually made of sheet-iron, in the
form of a cubical chest, with double walls, supported on four legs, as that of
Dr. Crookshank’s (Fig. 257). They are heated by gas or a lamp from below,
while the temperature is indicated by a thermometer inserted through a hole
in the top, as in that of the Hearson’s incubator. Test-tubes, flasks, funnels,
cotton-wool, &c., must be sterilised by exposure to a temperature of 150°C.
for an hour or more.
Wire Cages or crates are used for containing test-tubes, especially when
they are to be sterilised in the hot-air steriliser, or for lowering tubes of
nutrient jelly into the steam steriliser. All instruments, needles, scalpels,
&c., before using must be carefully sterilised.
Page 387
Steam Sterilisers are made either of iron or
tin, jacketed with thick felt, and provided
with a conical cap or lid perforated at the
apex to receive a thermometer (Fig. 258).
Inside the vessel is an iron grating or
diaphragm about two-thirds of the way
down, which divides the interior into two
chambers, the upper or steam chamber, and
the lower or water chamber. A gauge outside
marks the level of the water in the lower
chamber; this should be kept about two-
thirds full. The apparatus stands upon three
legs, and is heated from below with a Bunsen
burner or a lamp. It is employed for
sterilising nutrient media in tubes or flasks,
for cooking potatoes or hastening the
filtration of agar-agar. When the thermometer
indicates 100° C. the lid is removed, and test-
tubes are lowered in a wire-basket by means
of a hook and string, and the lid quickly
replaced. Potatoes or small flasks are
lowered into the cylinder in a tin receiver Fig. 258.—Dr. Koch’s Steam Steriliser.
with a perforated bottom, which rests upon
the grating, and admits of the contents being exposed to the steam
generated.
One of the most efficient forms of incubators introduced into the
bacteriological laboratory is that known as Hearson’s (Fig. 259). This
consists of a chamber surrounded by a water-jacket, with water space
below, to afford room for the pipe, L, which conveys the heated products
from the flame of the lamp, T, through the water and back again to the
lantern. A is the water-jacket surrounding the chamber containing the
cultures; O, the pipe through which the water supply is admitted; N, the tap
for employing the same; M, the overflow pipe; S, the capsule in a case
attached by a tube to the lower plate outside; D, a lever pivoted on the left,
carrying at its free end a damper, F, which, when resting on the chimney, V,
effectually closes it; P, a screw for adjusting the damper when starting the
tin, jacketed with thick felt, and provided
with a conical cap or lid perforated at the
apex to receive a thermometer (Fig. 258).
Inside the vessel is an iron grating or
diaphragm about two-thirds of the way
down, which divides the interior into two
chambers, the upper or steam chamber, and
the lower or water chamber. A gauge outside
marks the level of the water in the lower
chamber; this should be kept about two-
thirds full. The apparatus stands upon three
legs, and is heated from below with a Bunsen
burner or a lamp. It is employed for
sterilising nutrient media in tubes or flasks,
for cooking potatoes or hastening the
filtration of agar-agar. When the thermometer
indicates 100° C. the lid is removed, and test-
tubes are lowered in a wire-basket by means
of a hook and string, and the lid quickly
replaced. Potatoes or small flasks are
lowered into the cylinder in a tin receiver Fig. 258.—Dr. Koch’s Steam Steriliser.
with a perforated bottom, which rests upon
the grating, and admits of the contents being exposed to the steam
generated.
One of the most efficient forms of incubators introduced into the
bacteriological laboratory is that known as Hearson’s (Fig. 259). This
consists of a chamber surrounded by a water-jacket, with water space
below, to afford room for the pipe, L, which conveys the heated products
from the flame of the lamp, T, through the water and back again to the
lantern. A is the water-jacket surrounding the chamber containing the
cultures; O, the pipe through which the water supply is admitted; N, the tap
for employing the same; M, the overflow pipe; S, the capsule in a case
attached by a tube to the lower plate outside; D, a lever pivoted on the left,
carrying at its free end a damper, F, which, when resting on the chimney, V,
effectually closes it; P, a screw for adjusting the damper when starting the
Page 388
apparatus; H, a lead weight for bringing more pressure on the capsule; K, a
thermometer, the bulb of which is inside and the scale outside the chamber.
Fig. 259.—The Baird-Hearson Biological Incubator.
The treated products of combustion move in the direction indicated until the
water and chamber are sufficiently heated to distend the capsule. When this
point is reached the wire between S and P is pushed up by the capsule, and
the lever causes the damper to rise more or less off the chimney, V, and on
examining the thermometer the inside of the chamber is at length found to
remain steadily at the required temperature.
When the thermometer registers the desired temperature, the lead weight
must be damped to the lever by means of the milled-head screw which goes
through it. After having been once adjusted the heat in the interior will
thermometer, the bulb of which is inside and the scale outside the chamber.
Fig. 259.—The Baird-Hearson Biological Incubator.
The treated products of combustion move in the direction indicated until the
water and chamber are sufficiently heated to distend the capsule. When this
point is reached the wire between S and P is pushed up by the capsule, and
the lever causes the damper to rise more or less off the chimney, V, and on
examining the thermometer the inside of the chamber is at length found to
remain steadily at the required temperature.
When the thermometer registers the desired temperature, the lead weight
must be damped to the lever by means of the milled-head screw which goes
through it. After having been once adjusted the heat in the interior will
Page 389
remain constant, notwithstanding the utmost changes of temperature
occurring in these latitudes, nor will very great alterations in the size of the
lamp-flame seriously interfere with the results. The milled-head screw, P,
must be turned, after the first adjustment, during the whole time that the
incubator is in use. Observe the temperature before opening the door;
observations taken afterwards are worthless.
Preparation of Nutrient Media—Separation, and Cultivation of
Bacteria.
Fig. 260.—Plate Cultivation Showing Colonies.
To cultivate micro-organisms artificially they must be supplied with the
proper nutrient material, perfectly free from pre-existing organisms. The
secret of Koch’s methods greatly depends upon the possibility, in the case
of starting with a mixture of micro-organisms, of being able to isolate them
completely one from another, and to obtain an absolutely pure growth of
each cultivable species. When sterile nutrient gelatine has been liquefied in
a test-tube and inoculated with a mixture of bacteria in such a way that the
individual micro-organisms are distributed throughout it, and the liquid is
poured out on a glass plate and allowed to solidify, the individual bacteria,
instead of moving about freely as in a liquid medium, are fixed to one spot,
occurring in these latitudes, nor will very great alterations in the size of the
lamp-flame seriously interfere with the results. The milled-head screw, P,
must be turned, after the first adjustment, during the whole time that the
incubator is in use. Observe the temperature before opening the door;
observations taken afterwards are worthless.
Preparation of Nutrient Media—Separation, and Cultivation of
Bacteria.
Fig. 260.—Plate Cultivation Showing Colonies.
To cultivate micro-organisms artificially they must be supplied with the
proper nutrient material, perfectly free from pre-existing organisms. The
secret of Koch’s methods greatly depends upon the possibility, in the case
of starting with a mixture of micro-organisms, of being able to isolate them
completely one from another, and to obtain an absolutely pure growth of
each cultivable species. When sterile nutrient gelatine has been liquefied in
a test-tube and inoculated with a mixture of bacteria in such a way that the
individual micro-organisms are distributed throughout it, and the liquid is
poured out on a glass plate and allowed to solidify, the individual bacteria,
instead of moving about freely as in a liquid medium, are fixed to one spot,
Page 390
where they develop their own species. In this way colonies are formed, each
possessing its own biological characteristics and morphological
appearances (Fig. 260).
To maintain individuals isolated from each other during growth, and free
from contamination, it is only necessary to thin out the cultivation to protect
the plates from the air, and to have facilities for examining them from time
to time, and observing the characteristic microscopical appearances. The
colonies on nutrient gelatine examined with a low power (Fig. 260), if
micro-organisms such as Bacillus anthraces and Proteus mirabilis, the
naked eye appearances in test-tubes of the growth of the bacilli of anthrax
and tubercle, and the brilliant growth of micro-coccus prodigiosus, may be
given as examples in which the appearances are often very striking and
sometimes quite characteristic. I must, however, first direct attention to a
well-recognised fact, that bacteriology only touches animal pathology at a
few points, and that so far from bacteria being synonymous with disease
germs, the majority of these remarkable organisms appear to be beneficent
rather than inimical to man. This is of immense importance to science, as I
shall attempt to show further on; although even a brief description of all the
useful ferments due to bacteria and brought into use would occupy a
volume to themselves, and call for a school of bacteriology quite apart from
that involved in the medical aspect of the question, for the purpose of fully
investigating problems raised by the agriculturist, the forester, the gardener,
the dairyman, brewer, dyer, tanner, and other industries, which open up
vistas of practical application, and to some extent are already being taken
advantage of in commerce.
The Preparation of Nutrient Gelatine and Agar-agar.—Take half a
kilogramme (one pound) of beef as free as possible from fat, chop finely,
transfer to a flask or cylindrical vessel, and shake up well with a litre of
distilled water. Place the vessel in an ice-pail, or ice-cupboard, or in winter
in a cold cellar, and leave for the night. Next morning commence with the
preparation of all requisite apparatus. Thoroughly wash and rinse with
alcohol about 100 test-tubes, and allow them to dry. Plug the mouths of the
test-tubes with cotton-wool, place them in their wire cages in the hot-air
steriliser, to be heated for an hour at a temperature of 150°C. In the same
manner cleanse and sterilise several flasks, and a small glass funnel. In the
possessing its own biological characteristics and morphological
appearances (Fig. 260).
To maintain individuals isolated from each other during growth, and free
from contamination, it is only necessary to thin out the cultivation to protect
the plates from the air, and to have facilities for examining them from time
to time, and observing the characteristic microscopical appearances. The
colonies on nutrient gelatine examined with a low power (Fig. 260), if
micro-organisms such as Bacillus anthraces and Proteus mirabilis, the
naked eye appearances in test-tubes of the growth of the bacilli of anthrax
and tubercle, and the brilliant growth of micro-coccus prodigiosus, may be
given as examples in which the appearances are often very striking and
sometimes quite characteristic. I must, however, first direct attention to a
well-recognised fact, that bacteriology only touches animal pathology at a
few points, and that so far from bacteria being synonymous with disease
germs, the majority of these remarkable organisms appear to be beneficent
rather than inimical to man. This is of immense importance to science, as I
shall attempt to show further on; although even a brief description of all the
useful ferments due to bacteria and brought into use would occupy a
volume to themselves, and call for a school of bacteriology quite apart from
that involved in the medical aspect of the question, for the purpose of fully
investigating problems raised by the agriculturist, the forester, the gardener,
the dairyman, brewer, dyer, tanner, and other industries, which open up
vistas of practical application, and to some extent are already being taken
advantage of in commerce.
The Preparation of Nutrient Gelatine and Agar-agar.—Take half a
kilogramme (one pound) of beef as free as possible from fat, chop finely,
transfer to a flask or cylindrical vessel, and shake up well with a litre of
distilled water. Place the vessel in an ice-pail, or ice-cupboard, or in winter
in a cold cellar, and leave for the night. Next morning commence with the
preparation of all requisite apparatus. Thoroughly wash and rinse with
alcohol about 100 test-tubes, and allow them to dry. Plug the mouths of the
test-tubes with cotton-wool, place them in their wire cages in the hot-air
steriliser, to be heated for an hour at a temperature of 150°C. In the same
manner cleanse and sterilise several flasks, and a small glass funnel. In the
Page 391
meantime, the meat infusion must be well shaken, and the liquid portion
separated by filtering and squeezing through a linen cloth or a meat press.
The red juice thus obtained must be brought up to a litre by transferring it to
a large measuring glass and adding distilled water. It is then poured into a
sufficiently large and strong beaker, and set aside after the addition of ten
grammes of peptone, five grammes of common salt, and 100 grammes of
best gelatine.
In about half an hour the gelatine is sufficiently softened, and subsequent
heating in a water bath causes it to be completely dissolved.
The next process requires the greatest care and attention. Some micro-
organisms grow best in a slightly acid, others in a slightly alkaline, medium.
For example, for the growth and characteristic appearances of the comma
bacillus of Asiatic cholera a faintly alkaline soil is absolutely essential. This
slightly alkaline medium will be found to answer best for most micro-
organisms, and may be obtained as follows:—With a clean glass rod dipped
in the mixture, the reaction upon litmus-paper may be obtained, and a
concentrated solution of carbonate of soda must be added drop by drop until
red litmus-paper becomes faintly blue. If it is too alkaline, it can be
neutralised by the addition of lactic acid.
Finally, the mixture is heated for an hour in the water-bath. Ten minutes
before the boiling is completed the white of an egg beaten up with the shell
is added, and the liquid is then filtered while hot.
During filtration the funnel should be covered over with a plate of glass,
and the process of filtering must be repeated, if necessary, until a pale
straw-coloured, perfectly transparent filtrate results. The sterilised test-tubes
are filled to about a third of their depth by pouring in the gelatine carefully
and steadily. The object of this care is to prevent the mixture touching the
part of the tube with which the plug comes into contact; otherwise, when
the gelatine sets, the cotton-wool adheres to the tubes and becomes a source
of embarrassment to subsequent procedures. As the tubes are filled they are
placed in a basket, and then sterilised. They are either lowered into the
steam steriliser, when the thermometer indicates 100 cc., for twelve
minutes, for four or five successive days, or they may be transferred to the
separated by filtering and squeezing through a linen cloth or a meat press.
The red juice thus obtained must be brought up to a litre by transferring it to
a large measuring glass and adding distilled water. It is then poured into a
sufficiently large and strong beaker, and set aside after the addition of ten
grammes of peptone, five grammes of common salt, and 100 grammes of
best gelatine.
In about half an hour the gelatine is sufficiently softened, and subsequent
heating in a water bath causes it to be completely dissolved.
The next process requires the greatest care and attention. Some micro-
organisms grow best in a slightly acid, others in a slightly alkaline, medium.
For example, for the growth and characteristic appearances of the comma
bacillus of Asiatic cholera a faintly alkaline soil is absolutely essential. This
slightly alkaline medium will be found to answer best for most micro-
organisms, and may be obtained as follows:—With a clean glass rod dipped
in the mixture, the reaction upon litmus-paper may be obtained, and a
concentrated solution of carbonate of soda must be added drop by drop until
red litmus-paper becomes faintly blue. If it is too alkaline, it can be
neutralised by the addition of lactic acid.
Finally, the mixture is heated for an hour in the water-bath. Ten minutes
before the boiling is completed the white of an egg beaten up with the shell
is added, and the liquid is then filtered while hot.
During filtration the funnel should be covered over with a plate of glass,
and the process of filtering must be repeated, if necessary, until a pale
straw-coloured, perfectly transparent filtrate results. The sterilised test-tubes
are filled to about a third of their depth by pouring in the gelatine carefully
and steadily. The object of this care is to prevent the mixture touching the
part of the tube with which the plug comes into contact; otherwise, when
the gelatine sets, the cotton-wool adheres to the tubes and becomes a source
of embarrassment to subsequent procedures. As the tubes are filled they are
placed in a basket, and then sterilised. They are either lowered into the
steam steriliser, when the thermometer indicates 100 cc., for twelve
minutes, for four or five successive days, or they may be transferred to the
Page 392
test-tube water-bath, and heated for an hour or two for three successive
days.
If the gelatine shows any turbidity after, it must be poured back into a flask,
boiled for ten minutes, and filtered again, and the process of sterilisation
repeated.
Nutrient Agar-agar is a substance prepared from seaweed which grows on
the coasts of Japan and India, and is supplied in long crinkled strips. It boils
at 90° C., and remains solid up to a temperature of about 45° C. It is
therefore substituted for gelatine in the preparation of a jelly for the
cultivation of those bacteria which will grow best in the incubator at the
temperature of the blood, and also at ordinary temperature for bacteria
which lignify gelatine. The preparation is conducted on much the same
principles as those already described. Instead, however, of 100 grammes of
gelatine, only about twenty grammes of agar-agar (1·5 to 2 per cent.), and
to facilitate the solution it must be allowed to soak in salt water overnight.
Flannel is substituted for filter paper. The hot-water apparatus is invariably
employed. The final results, when solid, should be colourless and clear; but
if slightly milky, it may still be employed.
Wort-gelatine is used in studying the bacteria of fermentation. It is made by
adding from five to ten per cent. of gelatine to beer-wort.
Glycerine Agar-agar.—This is made by adding five per cent. of glycerine to
nutrient agar-agar, after the boiling and before the filtration.
days.
If the gelatine shows any turbidity after, it must be poured back into a flask,
boiled for ten minutes, and filtered again, and the process of sterilisation
repeated.
Nutrient Agar-agar is a substance prepared from seaweed which grows on
the coasts of Japan and India, and is supplied in long crinkled strips. It boils
at 90° C., and remains solid up to a temperature of about 45° C. It is
therefore substituted for gelatine in the preparation of a jelly for the
cultivation of those bacteria which will grow best in the incubator at the
temperature of the blood, and also at ordinary temperature for bacteria
which lignify gelatine. The preparation is conducted on much the same
principles as those already described. Instead, however, of 100 grammes of
gelatine, only about twenty grammes of agar-agar (1·5 to 2 per cent.), and
to facilitate the solution it must be allowed to soak in salt water overnight.
Flannel is substituted for filter paper. The hot-water apparatus is invariably
employed. The final results, when solid, should be colourless and clear; but
if slightly milky, it may still be employed.
Wort-gelatine is used in studying the bacteria of fermentation. It is made by
adding from five to ten per cent. of gelatine to beer-wort.
Glycerine Agar-agar.—This is made by adding five per cent. of glycerine to
nutrient agar-agar, after the boiling and before the filtration.
Page 393
Fig. 261.—Pure Cultivation in Tubes (Crookshank).
Test-tube Cultivations.—To inoculate test-tubes containing nutrient jelly,
the cotton-wool plug is removed. A sterilised needle, charged, for example,
with blood or pus containing bacteria, is thrust once in the middle line into
the nutrient jelly, and steadily withdrawn. The tube should be held
horizontally or with its mouth downwards, and the plug replaced as quickly
as possible, and an india-rubber cap fitted over the mouth of the tube.
The appearance produced by the growths in the test-tubes can be in most
cases sufficiently examined with the naked eye (Fig. 261). In some cases
the jelly is partially liquefied, while in others it remains solid. The growths
may be abundant or scanty, coloured or colourless. When liquefaction
slowly takes place in the needle tracts, the appearances which result are
often very delicate and in some very characteristic. The appearance of a
simple white thread with branching lateral filaments, of a cloudiness, or of a
string of beads in the track of the needle, may be given as examples. In
some cases much may be learnt by means of a magnifying-glass.
Beneke recommends that gelatine culture tubes should be inoculated by
making a puncture quite at the side of the medium, close to the glass. The
Test-tube Cultivations.—To inoculate test-tubes containing nutrient jelly,
the cotton-wool plug is removed. A sterilised needle, charged, for example,
with blood or pus containing bacteria, is thrust once in the middle line into
the nutrient jelly, and steadily withdrawn. The tube should be held
horizontally or with its mouth downwards, and the plug replaced as quickly
as possible, and an india-rubber cap fitted over the mouth of the tube.
The appearance produced by the growths in the test-tubes can be in most
cases sufficiently examined with the naked eye (Fig. 261). In some cases
the jelly is partially liquefied, while in others it remains solid. The growths
may be abundant or scanty, coloured or colourless. When liquefaction
slowly takes place in the needle tracts, the appearances which result are
often very delicate and in some very characteristic. The appearance of a
simple white thread with branching lateral filaments, of a cloudiness, or of a
string of beads in the track of the needle, may be given as examples. In
some cases much may be learnt by means of a magnifying-glass.
Beneke recommends that gelatine culture tubes should be inoculated by
making a puncture quite at the side of the medium, close to the glass. The
Page 394
advantage of this method over the plan of inoculating the mass in the
middle is that the growing culture can be microscopically examined from
the outside, and various details made out, such as the nature of the growth,
the comparative appearance of colonies near the surface and those situated
more deeply, and the presence of one or more distinct organisms. If the
tubes used have the opposite sides flat and parallel, such examinations will
be still further facilitated.
Plate Cultivations.—By this method a mixture of bacteria, whether in
fluids, excreta, or in cultivations on solid media, can be so treated that the
different species are isolated one from the other, and perfectly pure
cultivations of each of the cultivable bacteria in the original mixture
established in various nutrient media. We are enabled also to examine under
a low power of the microscope the individual colonies of bacteria. The
same process, with slight modification, is also employed in the examination
of air, soil, and water.
In order to spread out the liquid jelly evenly on the surface of a glass plate,
and to hasten its solidification, it is necessary to place the plate upon a level
and cool surface. The glass plates are sterilised in an iron box placed in the
hot-air steriliser, at 150° C., from one to two hours.
The damp chambers for the reception of the inoculated plates are prepared
by cleansing and washing out with one in twenty carbolic acid the shallow
glass dish and bell-cover (Fig. 253). A piece of filter-paper should cover the
bottom of dish, moistened with the same solution.
“In a glass-beaker with pad of cotton-wool at bottom place tube containing
cultivation, the three tubes to be inoculated, three glass rods which have to
be sterilised, and a thermometer. Liquefy the gelatine in the three tubes by
placing them in a beaker containing water 30° C. Keep the tubes, both
before and after the inoculation, in the warm water to maintain the gelatine
in a state of liquefaction. Remove the plug from the culture and also the
plug of test-tube with liquefied jelly. With the needle take up a droplet of
the cultivation and stir it round in the liquefied jelly. Replace both plugs,
and set aside the cultivation. Hold the freshly-inoculated tube almost
horizontally, then raise it to the vertical, so that the liquid gelatine gently
flows back. By repeating this motion, and rolling the tube, the micro-
middle is that the growing culture can be microscopically examined from
the outside, and various details made out, such as the nature of the growth,
the comparative appearance of colonies near the surface and those situated
more deeply, and the presence of one or more distinct organisms. If the
tubes used have the opposite sides flat and parallel, such examinations will
be still further facilitated.
Plate Cultivations.—By this method a mixture of bacteria, whether in
fluids, excreta, or in cultivations on solid media, can be so treated that the
different species are isolated one from the other, and perfectly pure
cultivations of each of the cultivable bacteria in the original mixture
established in various nutrient media. We are enabled also to examine under
a low power of the microscope the individual colonies of bacteria. The
same process, with slight modification, is also employed in the examination
of air, soil, and water.
In order to spread out the liquid jelly evenly on the surface of a glass plate,
and to hasten its solidification, it is necessary to place the plate upon a level
and cool surface. The glass plates are sterilised in an iron box placed in the
hot-air steriliser, at 150° C., from one to two hours.
The damp chambers for the reception of the inoculated plates are prepared
by cleansing and washing out with one in twenty carbolic acid the shallow
glass dish and bell-cover (Fig. 253). A piece of filter-paper should cover the
bottom of dish, moistened with the same solution.
“In a glass-beaker with pad of cotton-wool at bottom place tube containing
cultivation, the three tubes to be inoculated, three glass rods which have to
be sterilised, and a thermometer. Liquefy the gelatine in the three tubes by
placing them in a beaker containing water 30° C. Keep the tubes, both
before and after the inoculation, in the warm water to maintain the gelatine
in a state of liquefaction. Remove the plug from the culture and also the
plug of test-tube with liquefied jelly. With the needle take up a droplet of
the cultivation and stir it round in the liquefied jelly. Replace both plugs,
and set aside the cultivation. Hold the freshly-inoculated tube almost
horizontally, then raise it to the vertical, so that the liquid gelatine gently
flows back. By repeating this motion, and rolling the tube, the micro-
Page 395
organisms which have been introduced are distributed throughout the
gelatine. Any violent shaking, and consequent formation of bubbles, must
be carefully avoided. Inoculate the second tube, and also third, in the same
way, but with three droplets from a sterilised needle. The next process
consists in pouring out the gelatine on glass plates and allowing it to
solidify.
“Remove cover of box containing sterilised plates, withdraw a plate with
sterilised forceps, and rapidly transfer it to the filter-paper under the bell-
glass and quickly replace cover of box. Remove plug from the test-tube
which was first inoculated, and the contents are poured out on the plate.
With a glass rod the gelatine must be then rapidly spread out in an even
layer within about half an inch of the margin of the plate, the bell-glass is
replaced, and the gelatine is allowed to set. Meanwhile a glass bench is
placed in damp chamber, upon which the plate is placed when the gelatine
is quite solid; precisely the same process is repeated with the other tubes.
“The colonies will be found to develop in the course of a day or two, the
time varying with the temperature of the room. The lower plate will contain
a countless number of colonies, which, if the micro-organisms liquefy
gelatine, speedily commingle, and produce in a very short time a complete
liquefaction of the whole gelatine. On the middle plate the colonies will
also be very numerous, but retain their isolated positions for a longer time;
while on the uppermost plate the colonies are completely isolated from one
another, with an appreciable surface of gelatine intervening.
“The microscopical appearances of the colonies are best studied by placing
the plate on a slab of blackened glass, or on a porcelain slab if the colonies
are coloured. A small diaphragm is used, and the appearances studied
principally with a low power. A much simpler method of plate-cultivation is
to pour the liquefied jelly into shallow flat dishes; they take up much less
room, and in many ways are more convenient.
“Nutrient agar-agar can also be employed for the preparation of plate-
cultivations, but it is much more difficult to obtain satisfactory results.”
gelatine. Any violent shaking, and consequent formation of bubbles, must
be carefully avoided. Inoculate the second tube, and also third, in the same
way, but with three droplets from a sterilised needle. The next process
consists in pouring out the gelatine on glass plates and allowing it to
solidify.
“Remove cover of box containing sterilised plates, withdraw a plate with
sterilised forceps, and rapidly transfer it to the filter-paper under the bell-
glass and quickly replace cover of box. Remove plug from the test-tube
which was first inoculated, and the contents are poured out on the plate.
With a glass rod the gelatine must be then rapidly spread out in an even
layer within about half an inch of the margin of the plate, the bell-glass is
replaced, and the gelatine is allowed to set. Meanwhile a glass bench is
placed in damp chamber, upon which the plate is placed when the gelatine
is quite solid; precisely the same process is repeated with the other tubes.
“The colonies will be found to develop in the course of a day or two, the
time varying with the temperature of the room. The lower plate will contain
a countless number of colonies, which, if the micro-organisms liquefy
gelatine, speedily commingle, and produce in a very short time a complete
liquefaction of the whole gelatine. On the middle plate the colonies will
also be very numerous, but retain their isolated positions for a longer time;
while on the uppermost plate the colonies are completely isolated from one
another, with an appreciable surface of gelatine intervening.
“The microscopical appearances of the colonies are best studied by placing
the plate on a slab of blackened glass, or on a porcelain slab if the colonies
are coloured. A small diaphragm is used, and the appearances studied
principally with a low power. A much simpler method of plate-cultivation is
to pour the liquefied jelly into shallow flat dishes; they take up much less
room, and in many ways are more convenient.
“Nutrient agar-agar can also be employed for the preparation of plate-
cultivations, but it is much more difficult to obtain satisfactory results.”
Page 396
Microscopical Examination of Bacteria.
Bacteria in Liquids, Cultures, and Fresh Tissues.—In conducting
bacteriological researches, the importance of absolute cleanliness cannot be
too strongly insisted upon. All instruments, glass vessels, slides, and cover-
glasses should be thoroughly cleansed before use. The same applies to the
preparation and employment of culture media; any laxity in the processes of
sterilisation, or insufficient attention to minute technical details, will be
followed with disappointing results by contamination of the cultures,
resulting in the loss of much time.
For the preparation of microscopical specimens it will be found convenient
to use a platinum inoculating needle, sterilised, as before directed, in the
sheet-iron box; in a few moments it will be cool enough not to destroy the
bacteria with which it is brought into contact.
Unstained Bacteria.—The bacteria in liquids, such as blood and culture-
fluids, can be investigated in the unstained condition by transferring a drop
with a looped platinum needle, or a capillary pipette, to a slide, covering it
with a clean cover-glass, and examining without further treatment. If it is
desirable to keep the specimen under prolonged observation, a drop of
sterilised water or salt solution must be run in at the margin of the cover-
glass to counteract the tendency to dry.
Cultures on the solid media can be examined by transferring a small portion
with a sterilised needle to a drop of sterilised water on a slide, thinning it
out, and covering with cover-glass as already described. Tissues in the fresh
state may be teased out with needles (Fig. 249) in sterilised salt solution,
and pressed out into a sufficiently thin layer between the slide and cover-
glass. Glycerine may in many cases be substituted for salt solution,
especially for such as actinomyces and mould fungi.
Very small bacilli and micro-cocci are distinguished from granular matter or
fat-crystals, or vice versâ, by the fact that the latter are altered or dispersed
by the addition of acetic acid, and changed by solution of potash; ether
dissolves out fatty particles, while micro-organisms remain unaffected.
Baumgarten demonstrated tubercle bacilli in sections by treating them with
Bacteria in Liquids, Cultures, and Fresh Tissues.—In conducting
bacteriological researches, the importance of absolute cleanliness cannot be
too strongly insisted upon. All instruments, glass vessels, slides, and cover-
glasses should be thoroughly cleansed before use. The same applies to the
preparation and employment of culture media; any laxity in the processes of
sterilisation, or insufficient attention to minute technical details, will be
followed with disappointing results by contamination of the cultures,
resulting in the loss of much time.
For the preparation of microscopical specimens it will be found convenient
to use a platinum inoculating needle, sterilised, as before directed, in the
sheet-iron box; in a few moments it will be cool enough not to destroy the
bacteria with which it is brought into contact.
Unstained Bacteria.—The bacteria in liquids, such as blood and culture-
fluids, can be investigated in the unstained condition by transferring a drop
with a looped platinum needle, or a capillary pipette, to a slide, covering it
with a clean cover-glass, and examining without further treatment. If it is
desirable to keep the specimen under prolonged observation, a drop of
sterilised water or salt solution must be run in at the margin of the cover-
glass to counteract the tendency to dry.
Cultures on the solid media can be examined by transferring a small portion
with a sterilised needle to a drop of sterilised water on a slide, thinning it
out, and covering with cover-glass as already described. Tissues in the fresh
state may be teased out with needles (Fig. 249) in sterilised salt solution,
and pressed out into a sufficiently thin layer between the slide and cover-
glass. Glycerine may in many cases be substituted for salt solution,
especially for such as actinomyces and mould fungi.
Very small bacilli and micro-cocci are distinguished from granular matter or
fat-crystals, or vice versâ, by the fact that the latter are altered or dispersed
by the addition of acetic acid, and changed by solution of potash; ether
dissolves out fatty particles, while micro-organisms remain unaffected.
Baumgarten demonstrated tubercle bacilli in sections by treating them with
Page 397
potash, which clarified the tissues and brought the bacilli clearly into view.
In examining unstained bacteria the iris-diaphragm should be used, and the
sub-stage condenser carefully centred and focussed.
His’s Method of Staining.—A slide is prepared as for bacteria in the fresh
state; the reagents are then applied by placing them with a pipette drop by
drop at a margin of the cover-glass, and causing them to flow through the
preparation by means of a strip of filter-paper placed at the opposite margin.
Babès’ Method is as follows: A little of the growth spread out on a cover-
glass into as thin a film as possible; when almost dry, apply a drop or two of
a weak aqueous solution of methyl-violet from a pipette to the film; any
excess of the stain must be removed by gentle pressure with a strip of filter-
paper.
Cover-glass Preparations.—A cover-glass is smeared with the substance to
be examined spread out into a sufficiently thin layer; in the case of cultures
on solid media, diffuse the bacteria in a little sterilised water. By means of
another cover-glass the juice or fluid is squeezed out from between them
into a thin layer, and on sliding them apart each cover-glass bears on it a
thin film of the material. The cover-glass is then placed with its film side
upwards and allowed to dry. After a few minutes it is passed from above
downwards through the flame of a Bunsen burner three times. Apply two or
three drops of an aqueous solution of fuchsine or methyl-violet to cover the
film, wash away any surplus stain after a few minutes with distilled water.
The cover-glass is then allowed to dry, when the preparation may be
mounted in Canada balsam, or while still wet, turned over on a slide, and
the excess of water removed with filter-paper.
If necessary to apply stain for a much larger period, pour staining solution
into a watch glass and allow cover-glass to swim on surface with prepared
side downwards.
Crookshank, instead of watery solutions of aniline dyes, prefers to use
stronger solutions, and to reduce the staining by a momentary immersion in
alcohol. The method is as follows: cover-glass preparations are stained with
carbolised fuchsine (Neelsen’s solution) for about two minutes, rinsed in
In examining unstained bacteria the iris-diaphragm should be used, and the
sub-stage condenser carefully centred and focussed.
His’s Method of Staining.—A slide is prepared as for bacteria in the fresh
state; the reagents are then applied by placing them with a pipette drop by
drop at a margin of the cover-glass, and causing them to flow through the
preparation by means of a strip of filter-paper placed at the opposite margin.
Babès’ Method is as follows: A little of the growth spread out on a cover-
glass into as thin a film as possible; when almost dry, apply a drop or two of
a weak aqueous solution of methyl-violet from a pipette to the film; any
excess of the stain must be removed by gentle pressure with a strip of filter-
paper.
Cover-glass Preparations.—A cover-glass is smeared with the substance to
be examined spread out into a sufficiently thin layer; in the case of cultures
on solid media, diffuse the bacteria in a little sterilised water. By means of
another cover-glass the juice or fluid is squeezed out from between them
into a thin layer, and on sliding them apart each cover-glass bears on it a
thin film of the material. The cover-glass is then placed with its film side
upwards and allowed to dry. After a few minutes it is passed from above
downwards through the flame of a Bunsen burner three times. Apply two or
three drops of an aqueous solution of fuchsine or methyl-violet to cover the
film, wash away any surplus stain after a few minutes with distilled water.
The cover-glass is then allowed to dry, when the preparation may be
mounted in Canada balsam, or while still wet, turned over on a slide, and
the excess of water removed with filter-paper.
If necessary to apply stain for a much larger period, pour staining solution
into a watch glass and allow cover-glass to swim on surface with prepared
side downwards.
Crookshank, instead of watery solutions of aniline dyes, prefers to use
stronger solutions, and to reduce the staining by a momentary immersion in
alcohol. The method is as follows: cover-glass preparations are stained with
carbolised fuchsine (Neelsen’s solution) for about two minutes, rinsed in
Page 398
alcohol for a few seconds, and quickly washed in water. This method is
specially valuable for sarcinæ and streptococci.
Gram’s Method.—The whole film is first stained violet with gentian-violet,
fixed by a solution of iodine, in iodide of potassium in the bacilli, but not in
any débris, pus cells, or tissue elements present. Transfer cover-glass to
alcohol, the bacilli alone remain stained, the violet colour being changed to
blue. By employing a contrast colour, such as eosin, a double staining is
obtained.
For staining preparations with gentian-violet Crookshank employs the
following useful method:—Place four or five drops of pure aniline in a test-
tube, add distilled water to three-quarters full, close mouth with thumb,
shake thoroughly. Filter the emulsion twice, pour filtrate into watch-glass.
To the perfectly clear aniline water thus obtained, add, drop by drop, a
concentrated alcoholic solution of gentian-violet till precipitation
commences. Cover-glasses must be left in this solution ten minutes,
transferred to iodine-potassic-iodide until the film becomes uniformly
brown, then rinsed in alcohol. The decolourisation may be hastened by
dipping the cover-glass in clove oil and returning to alcohol. Again immerse
cover-glass in clove oil, dry by gently pressing between two layers of filter-
paper, and mount in Canada balsam.
Double-staining of cover-glass preparations.—They can be treated by
Ehrlich’s method for staining tubercular sputum, or by Neelsen’s
modification, or by staining with eosin after treatment by the method of
Gram.
Ehrlich’s Method is as follows: Five parts of aniline oil are shaken up with
one hundred parts of distilled water, and the emulsion filtered through
moistened filter-paper. A saturated alcoholic solution of fuchsine, methyl-
violet, or gentian-violet, is added to filtrate in watch-glass, drop by drop,
until precipitation commences. Cover-glass preparations are floated in this
mixture for fifteen minutes to half an hour, then washed for a few seconds
in dilute nitric acid (one part of nitric acid to two of water), then rinsed in
distilled water.
specially valuable for sarcinæ and streptococci.
Gram’s Method.—The whole film is first stained violet with gentian-violet,
fixed by a solution of iodine, in iodide of potassium in the bacilli, but not in
any débris, pus cells, or tissue elements present. Transfer cover-glass to
alcohol, the bacilli alone remain stained, the violet colour being changed to
blue. By employing a contrast colour, such as eosin, a double staining is
obtained.
For staining preparations with gentian-violet Crookshank employs the
following useful method:—Place four or five drops of pure aniline in a test-
tube, add distilled water to three-quarters full, close mouth with thumb,
shake thoroughly. Filter the emulsion twice, pour filtrate into watch-glass.
To the perfectly clear aniline water thus obtained, add, drop by drop, a
concentrated alcoholic solution of gentian-violet till precipitation
commences. Cover-glasses must be left in this solution ten minutes,
transferred to iodine-potassic-iodide until the film becomes uniformly
brown, then rinsed in alcohol. The decolourisation may be hastened by
dipping the cover-glass in clove oil and returning to alcohol. Again immerse
cover-glass in clove oil, dry by gently pressing between two layers of filter-
paper, and mount in Canada balsam.
Double-staining of cover-glass preparations.—They can be treated by
Ehrlich’s method for staining tubercular sputum, or by Neelsen’s
modification, or by staining with eosin after treatment by the method of
Gram.
Ehrlich’s Method is as follows: Five parts of aniline oil are shaken up with
one hundred parts of distilled water, and the emulsion filtered through
moistened filter-paper. A saturated alcoholic solution of fuchsine, methyl-
violet, or gentian-violet, is added to filtrate in watch-glass, drop by drop,
until precipitation commences. Cover-glass preparations are floated in this
mixture for fifteen minutes to half an hour, then washed for a few seconds
in dilute nitric acid (one part of nitric acid to two of water), then rinsed in
distilled water.
Page 399
Neelsen’s Solution and Methylene Blue.—Ziehl suggested the use of
carbolic acid as a substitute for aniline blue. Neelsen recommended a
solution of carbolic acid, absolute alcohol and fuchsine. (See Appendix.)
Gram’s Solution and Eosin.—After using Gram’s method as above and
decolourising in alcohol, the cover-glass is placed in a weak solution of
eosin for two or three minutes, washed in alcohol, immersed in clove oil,
dried, and mounted in balsam.
Staining of Spores.—The cover-glass preparation must be heated to 210° C.
for half an hour, or passed about twelve times through the flame of a
Bunsen burner, or exposed to the action of strong sulphuric acid for several
seconds, then a few drops of a watery solution of aniline dye applied in the
usual way. To double-stain spore-bearing bacilli the cover-glass preparation
must be floated from twenty minutes to an hour on Ehrlich’s fuchsine-
aniline-water, or on the Ziehl-Neelsen solution. The stain must be heated
until steam arises.
Staining of Flagella.
Koch first stained flagella by floating the cover-glass on a watery solution
of hæmatoxylin, transferring them to a five per cent. solution of chromic
acid, or to Müller’s fluid, by which they obtained a brownish-black
coloration.
Löffler’s Method.—Add together aqueous solutions of ferrous-sulphate and
tannin (twenty per cent.) until the mixture turns a violet-black colour, then
add three or four cc. of a one-in-eight aqueous solution of logwood; a few
drops of carbolic acid may be added before transferring to a stoppered
bottle; that is the mordant. The dye consists of 1 cc. of a one per cent.
solution of caustic soda, added to 100 cc. of aniline water, in which four or
five grammes of either methyl-violet, methylene blue, or fuchsine, are
dissolved. A cover-glass preparation is made in the usual way, then the film
is covered with mordant, and cover-glass held over flame until steam rises,
the mordant is then washed off with distilled water. The stain is filtered and
a few drops allowed to fall on film, after a few minutes the cover-glass is
carbolic acid as a substitute for aniline blue. Neelsen recommended a
solution of carbolic acid, absolute alcohol and fuchsine. (See Appendix.)
Gram’s Solution and Eosin.—After using Gram’s method as above and
decolourising in alcohol, the cover-glass is placed in a weak solution of
eosin for two or three minutes, washed in alcohol, immersed in clove oil,
dried, and mounted in balsam.
Staining of Spores.—The cover-glass preparation must be heated to 210° C.
for half an hour, or passed about twelve times through the flame of a
Bunsen burner, or exposed to the action of strong sulphuric acid for several
seconds, then a few drops of a watery solution of aniline dye applied in the
usual way. To double-stain spore-bearing bacilli the cover-glass preparation
must be floated from twenty minutes to an hour on Ehrlich’s fuchsine-
aniline-water, or on the Ziehl-Neelsen solution. The stain must be heated
until steam arises.
Staining of Flagella.
Koch first stained flagella by floating the cover-glass on a watery solution
of hæmatoxylin, transferring them to a five per cent. solution of chromic
acid, or to Müller’s fluid, by which they obtained a brownish-black
coloration.
Löffler’s Method.—Add together aqueous solutions of ferrous-sulphate and
tannin (twenty per cent.) until the mixture turns a violet-black colour, then
add three or four cc. of a one-in-eight aqueous solution of logwood; a few
drops of carbolic acid may be added before transferring to a stoppered
bottle; that is the mordant. The dye consists of 1 cc. of a one per cent.
solution of caustic soda, added to 100 cc. of aniline water, in which four or
five grammes of either methyl-violet, methylene blue, or fuchsine, are
dissolved. A cover-glass preparation is made in the usual way, then the film
is covered with mordant, and cover-glass held over flame until steam rises,
the mordant is then washed off with distilled water. The stain is filtered and
a few drops allowed to fall on film, after a few minutes the cover-glass is
Page 400
again warmed until steam rises. The stain is then washed off with distilled
water, and the preparation is ready to be mounted for examination.
As Löffler’s process is somewhat complicated, a modification has been said
to afford more satisfactory results. A specimen is taken from a recent
gelatine culture and diluted with water. A little of the fluid is then
transferred to a warm cover-glass by means of a pipette and allowed to dry,
after which a drop of the following mordant is applied:—Aqueous solution
of tannin (twenty per cent.), ten cc.; cold saturated solution of ferrous
sulphate, five cc.; saturated solution of fuchsine in absolute alcohol, one cc.
The cover is next heated gently for a short time until vapours are given off,
then washed carefully. This process is repeated two or three times, and the
specimen washed after each application. Subsequently, staining is effected
by means of Ziehl’s fuchsine solution, the cover is afterwards warmed once
or twice for about fifteen seconds, then washed, and the specimen examined
in water to ascertain if the colour is sufficiently intense. If satisfactory, the
preparation may then be dried and finally mounted in Canada balsam or
dammar.
Preservation of Preparations.—After examining a cover-glass preparation
with an oil-immersion objective the cedar oil must be carefully wiped off,
and the slide set aside for the Canada balsam to set. At a convenient time
these preparations should be sealed with a ring of Hollis’s glue.
Bacteria in Sections of Tissues.
Method of Hardening and Decalcifying Tissues.—To harden small organs,
such as the viscera of a mouse, they should be placed on a piece of filter-
paper at the bottom of a small wide-mouthed glass jar, and covered with
about twenty times their volume of absolute alcohol. Larger organs are
treated in the same way, but must be cut up into small pieces. Müller’s
fluid, methylated spirit, or formalin may be used.
Teeth, or osseous structures, must first be placed in a decalcifying solution,
as Kleinenberg’s. When sufficiently softened, soak in water, to wash out
picric acid, and transfer to weak spirit. Ebner’s solution gives good results.
water, and the preparation is ready to be mounted for examination.
As Löffler’s process is somewhat complicated, a modification has been said
to afford more satisfactory results. A specimen is taken from a recent
gelatine culture and diluted with water. A little of the fluid is then
transferred to a warm cover-glass by means of a pipette and allowed to dry,
after which a drop of the following mordant is applied:—Aqueous solution
of tannin (twenty per cent.), ten cc.; cold saturated solution of ferrous
sulphate, five cc.; saturated solution of fuchsine in absolute alcohol, one cc.
The cover is next heated gently for a short time until vapours are given off,
then washed carefully. This process is repeated two or three times, and the
specimen washed after each application. Subsequently, staining is effected
by means of Ziehl’s fuchsine solution, the cover is afterwards warmed once
or twice for about fifteen seconds, then washed, and the specimen examined
in water to ascertain if the colour is sufficiently intense. If satisfactory, the
preparation may then be dried and finally mounted in Canada balsam or
dammar.
Preservation of Preparations.—After examining a cover-glass preparation
with an oil-immersion objective the cedar oil must be carefully wiped off,
and the slide set aside for the Canada balsam to set. At a convenient time
these preparations should be sealed with a ring of Hollis’s glue.
Bacteria in Sections of Tissues.
Method of Hardening and Decalcifying Tissues.—To harden small organs,
such as the viscera of a mouse, they should be placed on a piece of filter-
paper at the bottom of a small wide-mouthed glass jar, and covered with
about twenty times their volume of absolute alcohol. Larger organs are
treated in the same way, but must be cut up into small pieces. Müller’s
fluid, methylated spirit, or formalin may be used.
Teeth, or osseous structures, must first be placed in a decalcifying solution,
as Kleinenberg’s. When sufficiently softened, soak in water, to wash out
picric acid, and transfer to weak spirit. Ebner’s solution gives good results.
Page 401
Methods of embedding, fixing, and cutting.—Crookshank finds that after
hardening, the pieces of tissue are embedded in a mixture of ether and
alcohol for an hour or more, then transferred to a solution of celloidin in
equal parts of ether and alcohol, and left there for several hours.
The piece of tissue is then placed in a glass capsule, and some of the
celloidin solution poured over it. The capsule can be placed bodily in 60 to
80 per cent. alcohol, and left there until the following morning. The
celloidin should be of the consistency of wax. The piece of tissue is next cut
out, and after trimming is put into water until it sinks, then transferred to
gum, and cut with the freezing microtome.
Sections of fresh tissues are to be floated in ·8 per cent. salt solution, and
then carefully transferred by a platinum lifter to a watch-glass containing
absolute alcohol.
Staining Bacteria in Tissue Sections.—Weigert’s method is as follows:—
Place sections for from six to eighteen hours in a one per cent. watery
solution of any of the basic aniline dyes. To hasten, place the capsule
containing solution in the incubator, or heat it to 45° C., or a stronger
solution may be used. In the latter case the sections must be treated with a
half-saturated solution of carbonate of potash, as they are easily over-
stained. In either case the sections are next washed with distilled water,
passed through sixty per cent. alcohol into absolute alcohol. When almost
decolourised, spread out on a platinum lifter and transfer to clove oil, or
stain with picro-carmine solution (Weigert’s) for half an hour, wash in
water, alcohol, and treat with clove oil, and transfer to clean glass slide.
Gram’s Method.—Sections are stained for ten minutes in a capsule
containing aniline-gentian-violet solution, then placed in the iodine and
iodide solution until uniformly brown, then placed in absolute alcohol, and
washed by carefully moving sections in the liquid with a glass rod. When
completely decolourised, they are transferred to clove oil and then to a
slide.
Double-staining is obtained by transferring the sections after
decolourisation to eosin, Bismarck brown, or vesuvin (Crookshank).
hardening, the pieces of tissue are embedded in a mixture of ether and
alcohol for an hour or more, then transferred to a solution of celloidin in
equal parts of ether and alcohol, and left there for several hours.
The piece of tissue is then placed in a glass capsule, and some of the
celloidin solution poured over it. The capsule can be placed bodily in 60 to
80 per cent. alcohol, and left there until the following morning. The
celloidin should be of the consistency of wax. The piece of tissue is next cut
out, and after trimming is put into water until it sinks, then transferred to
gum, and cut with the freezing microtome.
Sections of fresh tissues are to be floated in ·8 per cent. salt solution, and
then carefully transferred by a platinum lifter to a watch-glass containing
absolute alcohol.
Staining Bacteria in Tissue Sections.—Weigert’s method is as follows:—
Place sections for from six to eighteen hours in a one per cent. watery
solution of any of the basic aniline dyes. To hasten, place the capsule
containing solution in the incubator, or heat it to 45° C., or a stronger
solution may be used. In the latter case the sections must be treated with a
half-saturated solution of carbonate of potash, as they are easily over-
stained. In either case the sections are next washed with distilled water,
passed through sixty per cent. alcohol into absolute alcohol. When almost
decolourised, spread out on a platinum lifter and transfer to clove oil, or
stain with picro-carmine solution (Weigert’s) for half an hour, wash in
water, alcohol, and treat with clove oil, and transfer to clean glass slide.
Gram’s Method.—Sections are stained for ten minutes in a capsule
containing aniline-gentian-violet solution, then placed in the iodine and
iodide solution until uniformly brown, then placed in absolute alcohol, and
washed by carefully moving sections in the liquid with a glass rod. When
completely decolourised, they are transferred to clove oil and then to a
slide.
Double-staining is obtained by transferring the sections after
decolourisation to eosin, Bismarck brown, or vesuvin (Crookshank).
Page 402
Formalin is an excellent preservative fluid; one part to 20,000 is sufficient
to prevent fermentation. For the preservation of vegetable sections, a one
per cent. solution is required; even the fresh appearance of vegetable
structures is preserved for some time when immersed in it. In the nutrient
gelatine for biological specimens, if used early, will arrest the liquefaction
of the gelatine by bacteria. For hardening it saves time, and is even better
than alcohol, chromic acid, pot. bich., and many others. It does not cause
shrinkage of the cells. Tissue ½ to ¾ inch thick hardens in twenty-four
hours in pure formalin; five to ten per cent. is best for loose tissue. In
another method, by which time can be saved, instead of placing the
specimen in the formalin and afterwards in mucilage, prior to cutting
sections, make the mucilage with two per cent. (or stronger) formalin water,
and it will then answer both purposes at the same time.
Preparing, Mounting, Cementing and Collecting Objects.
Various materials are required for preparing and mounting microscopic
objects, as slips of glass, patent flatted plate measuring 3 × 1 inch, thin glass
covers, glass cells, preservative media, varnishes, cements, a glazier’s
diamond, and a Shadbolt’s turn-table.
The glass slides and covers, although sent out packed ready for use, should
be immersed in an alkaline solution to ensure perfect freedom from any
greasiness derived from touching by the fingers. Dr. Seller recommends a
particular solution for this purpose. (See Formulæ, Appendix.)
Varnishes and cements must be selected with care, as these are not only
expected to adhere firmly to the glass slide, but also to resist the action of
the preservative fluid in which the specimen may be mounted. Among the
numerous preparations employed, I may enumerate Canada balsam, gum
dammar, Venice turpentine, Japanners’ gold size, used for closing up cells,
asphalte varnish, Brunswick black, shellac, glue and honey, Hollis’ liquid
glue, and marine glue. To give a finish to the mounted specimen, coloured
varnishes are sometimes resorted to. A red varnish of sealing-wax is made
by digesting powdered sealing-wax in strong alcohol. Filter, and place the
solution in a dish, and evaporate by means of a sand bath to reduce it to a
to prevent fermentation. For the preservation of vegetable sections, a one
per cent. solution is required; even the fresh appearance of vegetable
structures is preserved for some time when immersed in it. In the nutrient
gelatine for biological specimens, if used early, will arrest the liquefaction
of the gelatine by bacteria. For hardening it saves time, and is even better
than alcohol, chromic acid, pot. bich., and many others. It does not cause
shrinkage of the cells. Tissue ½ to ¾ inch thick hardens in twenty-four
hours in pure formalin; five to ten per cent. is best for loose tissue. In
another method, by which time can be saved, instead of placing the
specimen in the formalin and afterwards in mucilage, prior to cutting
sections, make the mucilage with two per cent. (or stronger) formalin water,
and it will then answer both purposes at the same time.
Preparing, Mounting, Cementing and Collecting Objects.
Various materials are required for preparing and mounting microscopic
objects, as slips of glass, patent flatted plate measuring 3 × 1 inch, thin glass
covers, glass cells, preservative media, varnishes, cements, a glazier’s
diamond, and a Shadbolt’s turn-table.
The glass slides and covers, although sent out packed ready for use, should
be immersed in an alkaline solution to ensure perfect freedom from any
greasiness derived from touching by the fingers. Dr. Seller recommends a
particular solution for this purpose. (See Formulæ, Appendix.)
Varnishes and cements must be selected with care, as these are not only
expected to adhere firmly to the glass slide, but also to resist the action of
the preservative fluid in which the specimen may be mounted. Among the
numerous preparations employed, I may enumerate Canada balsam, gum
dammar, Venice turpentine, Japanners’ gold size, used for closing up cells,
asphalte varnish, Brunswick black, shellac, glue and honey, Hollis’ liquid
glue, and marine glue. To give a finish to the mounted specimen, coloured
varnishes are sometimes resorted to. A red varnish of sealing-wax is made
by digesting powdered sealing-wax in strong alcohol. Filter, and place the
solution in a dish, and evaporate by means of a sand bath to reduce it to a
Page 403
proper consistency. This is said to resist the action of cedar oil. For white,
zinc, cement is the best. This is made of benzole, gum dammar, oxide of
zinc, and turpentine. Cole gives another formula, but either of these may be
obtained of Squire, who supplies every kind of staining and mounting
material.
Fig. 262.—Walmsley’s Cell-making Turn-table.
Cells for Mounting.—The minuter forms of life should be mounted in thin
cells, which may be readily made with Japanners’ gold size, dammar or
asphalte, and a Shadbolt or Walmsley’s turntable. The glass slide being
placed under the metal springs in such a manner that its two ends shall be
equi-distant from the centre (a guide to the position is afforded by the
circles traced out on the brass), take a camel’s hair pencil and dip it into the
Japanner’s gold-size, holding it firmly between the finger and thumb, and
set the wheel in motion, when a perfect circle will be formed; put it aside to
dry, or place it in the warm chamber to harden. To cut cover-glasses place a
sheet of thin glass under the brass springs, and substitute for the pencil a
cutting diamond. A cutting diamond is not only useful to the microscopist
for the above purpose, but also for writing the names of mounted objects on
one end of the slide.
It will be found convenient to make a number of such cells, and keep a
stock ready for use. There are many objects whose structure is very
transparent. These should be mounted dry. Scales from the wings of
butterflies and moths, of the podura and lepisma, and some of the
diatomaceæ are of this class. All that is necessary in preparing objects for
dry mounting is to take care that they are free from extraneous matter, and
zinc, cement is the best. This is made of benzole, gum dammar, oxide of
zinc, and turpentine. Cole gives another formula, but either of these may be
obtained of Squire, who supplies every kind of staining and mounting
material.
Fig. 262.—Walmsley’s Cell-making Turn-table.
Cells for Mounting.—The minuter forms of life should be mounted in thin
cells, which may be readily made with Japanners’ gold size, dammar or
asphalte, and a Shadbolt or Walmsley’s turntable. The glass slide being
placed under the metal springs in such a manner that its two ends shall be
equi-distant from the centre (a guide to the position is afforded by the
circles traced out on the brass), take a camel’s hair pencil and dip it into the
Japanner’s gold-size, holding it firmly between the finger and thumb, and
set the wheel in motion, when a perfect circle will be formed; put it aside to
dry, or place it in the warm chamber to harden. To cut cover-glasses place a
sheet of thin glass under the brass springs, and substitute for the pencil a
cutting diamond. A cutting diamond is not only useful to the microscopist
for the above purpose, but also for writing the names of mounted objects on
one end of the slide.
It will be found convenient to make a number of such cells, and keep a
stock ready for use. There are many objects whose structure is very
transparent. These should be mounted dry. Scales from the wings of
butterflies and moths, of the podura and lepisma, and some of the
diatomaceæ are of this class. All that is necessary in preparing objects for
dry mounting is to take care that they are free from extraneous matter, and
Page 404
fix them permanently in the position in which their structure will show to
the best advantage.
For mounting specimens of greater thickness it is desirable to use deeper
cells. It will then be found convenient to make a second or a third
application of the gold-size, allowing sufficient time between applications
for the varnish to dry. Cells of a still deeper kind are made up by cementing
rings of glass or metal to the glass-slides with marine glue or Brunswick
black. The latter will be rendered more durable by mixing in a small
quantity of indiarubber varnish (made by dissolving small strips of
caoutchouc in gas-tar). The process of mounting in glass-cells is similar to
that employed in making varnish-cells, except that a somewhat larger
quantity of cementing medium is required. Objects mounted in this way
should be kept for a time in the horizontal position, and a little fresh varnish
must be applied if the cement shows a tendency to crack. In mounting
objects in balsam, care must be taken to have the specimen quite dry before
transferring it to turpentine. Objects mounted in cells should become
perfectly saturated with the mounting fluid before being finally cemented
down.
It is preferable to mount and preserve
specimens of animal tissues in shallow cells,
to avoid undue pressure on the preparation.
Cells intended to contain preparations
immersed in fluid must be made of a
substance impervious to the fluid used, such as
Fig. 263.—Glass-cells for Mounting.
here represented (Fig. 263). The surface of the
fixed glass-circle should be slightly roughened
before applying the cement.
Different modes of mounting may be employed with advantage; for
instance, entomological specimens, as legs, wings, spiracles, tracheæ,
ovipositors, stings, tongues, palates, corneæ, should be mounted in balsam;
the trachea of the house-cricket, however, should be mounted dry. Sections
of bone may either be mounted dry or in a fluid. Other objects, as sections
of wood and stones of fruit, exhibit their structure best in Canada balsam.
the best advantage.
For mounting specimens of greater thickness it is desirable to use deeper
cells. It will then be found convenient to make a second or a third
application of the gold-size, allowing sufficient time between applications
for the varnish to dry. Cells of a still deeper kind are made up by cementing
rings of glass or metal to the glass-slides with marine glue or Brunswick
black. The latter will be rendered more durable by mixing in a small
quantity of indiarubber varnish (made by dissolving small strips of
caoutchouc in gas-tar). The process of mounting in glass-cells is similar to
that employed in making varnish-cells, except that a somewhat larger
quantity of cementing medium is required. Objects mounted in this way
should be kept for a time in the horizontal position, and a little fresh varnish
must be applied if the cement shows a tendency to crack. In mounting
objects in balsam, care must be taken to have the specimen quite dry before
transferring it to turpentine. Objects mounted in cells should become
perfectly saturated with the mounting fluid before being finally cemented
down.
It is preferable to mount and preserve
specimens of animal tissues in shallow cells,
to avoid undue pressure on the preparation.
Cells intended to contain preparations
immersed in fluid must be made of a
substance impervious to the fluid used, such as
Fig. 263.—Glass-cells for Mounting.
here represented (Fig. 263). The surface of the
fixed glass-circle should be slightly roughened
before applying the cement.
Different modes of mounting may be employed with advantage; for
instance, entomological specimens, as legs, wings, spiracles, tracheæ,
ovipositors, stings, tongues, palates, corneæ, should be mounted in balsam;
the trachea of the house-cricket, however, should be mounted dry. Sections
of bone may either be mounted dry or in a fluid. Other objects, as sections
of wood and stones of fruit, exhibit their structure best in Canada balsam.
Page 405
In mounting entomological specimens, the first thing, of course, is the
dissection of the insect. This is best accomplished by the aid of a dissecting
microscope, a pair of small brass forceps, and finely-pointed scissors; the
parts to be prepared and mounted should first be carefully detached from
the insect with the scissors, then immersed in a solution of caustic alkali
(liquor potassæ) for a few days, to soften and dissolve out the fat and soft
parts. The length of time necessary for their immersion can only be
determined by experience, but, as a general rule, the objects assume a
certain amount of transparency when they have been long enough in the
alkali; when this is ascertained, the object must be placed in a proper
receptacle and put by to soak for two or three hours in soft or distilled
water. It should then be placed between two slips of glass, and gently
pressed till the softer parts are removed. Should any adhere to the edge of
the object, it will be necessary to wash the specimen carefully in water, a
process that will be much assisted by the delicate touches of a camel’s-hair
brush. Place the object now and then under the microscope to see that all
extraneous matter is removed, and when this is accomplished take the
specimen up carefully with the camel’s-hair brush, or a lifter, and place it on
a piece of very smooth paper (thick ivory note is the best for the purpose),
arrange it carefully with the brush and a finely pointed needle, place a
second piece of paper over it, and press it flat between two slips of glass,
and compress it by a small spring clip (Fig. 264). A dozen clips may be had
for a few pence. When thoroughly dry (which it will probably be in about
twenty-four hours, if in a warm room), separate the glasses, and gently
unfold the paper; then, with a little careful manipulation, the object may be
readily detached, and placed in a little spirit of turpentine, where it should
be allowed to remain until rendered transparent and fit for mounting. The
time during which it should remain in this liquid will depend on the
structure; some objects, such as wings of flies, will be quickly permeated,
while horny and dense objects require an immersion of a fortnight or even
longer. A pomatum pot with a concave bottom and well-fitting lid will
answer admirably for conducting the soaking process in; and it is well, in
preparing several specimens at a time, to have two pots, one for large and
medium, the other for very small objects, otherwise the smaller will adhere
to the larger.
dissection of the insect. This is best accomplished by the aid of a dissecting
microscope, a pair of small brass forceps, and finely-pointed scissors; the
parts to be prepared and mounted should first be carefully detached from
the insect with the scissors, then immersed in a solution of caustic alkali
(liquor potassæ) for a few days, to soften and dissolve out the fat and soft
parts. The length of time necessary for their immersion can only be
determined by experience, but, as a general rule, the objects assume a
certain amount of transparency when they have been long enough in the
alkali; when this is ascertained, the object must be placed in a proper
receptacle and put by to soak for two or three hours in soft or distilled
water. It should then be placed between two slips of glass, and gently
pressed till the softer parts are removed. Should any adhere to the edge of
the object, it will be necessary to wash the specimen carefully in water, a
process that will be much assisted by the delicate touches of a camel’s-hair
brush. Place the object now and then under the microscope to see that all
extraneous matter is removed, and when this is accomplished take the
specimen up carefully with the camel’s-hair brush, or a lifter, and place it on
a piece of very smooth paper (thick ivory note is the best for the purpose),
arrange it carefully with the brush and a finely pointed needle, place a
second piece of paper over it, and press it flat between two slips of glass,
and compress it by a small spring clip (Fig. 264). A dozen clips may be had
for a few pence. When thoroughly dry (which it will probably be in about
twenty-four hours, if in a warm room), separate the glasses, and gently
unfold the paper; then, with a little careful manipulation, the object may be
readily detached, and placed in a little spirit of turpentine, where it should
be allowed to remain until rendered transparent and fit for mounting. The
time during which it should remain in this liquid will depend on the
structure; some objects, such as wings of flies, will be quickly permeated,
while horny and dense objects require an immersion of a fortnight or even
longer. A pomatum pot with a concave bottom and well-fitting lid will
answer admirably for conducting the soaking process in; and it is well, in
preparing several specimens at a time, to have two pots, one for large and
medium, the other for very small objects, otherwise the smaller will adhere
to the larger.
Page 406
In mounting objects in fluid, the glass
cover should come nearly, but not quite, to
the edge of the cell, a slight margin being
left for the cement, which should project
slightly over the edge of the cover, in order
to secure it to the cell.
Media for Preserving Algæ.—The most
Fig. 264.—Spring Clip for Mounting.
useful preservative media for algæ are
chrome-alum, formalin, and camphor water. The solution should consist of
one per cent. of chrome-alum and one per cent. of formalin; this will render
the gelatinous sheath and matrix form clear, while it will retain the colour of
the algæ in most cases. The Chlorophyceæ do well in any of these media;
but other species, as Ulva Lactuca, are rendered somewhat brittle. For such
use formalin alone. The Phæophyceæ should be placed while fresh in the
formalin; the larger forms are better fixed by placing them for an hour or
two in chrome-alum solution. The Florideæ do well in any of the three
solutions, but the more delicate species, Griffithsia, require a two per cent.
formalin solution in sea-water; the plant preserves its natural appearance in
this medium.
To preserve and mount diatomaceæ in as nearly as possible a natural
condition, they should be first well washed in distilled water and mounted
in a medium composed of one part of spirits of wine to seven parts of
distilled water. The siliceous coverings of the diatoms, however, which
show various beautiful forms under the higher powers of the microscope,
require more care in preparation. The guano, or infusorial earth containing
them, should first be washed several times in water till the water is
colourless, allowing sufficient time for precipitation between each washing.
The deposit must then be put into a test tube and nitro-hydrochloric acid
(equal parts of nitric and hydrochloric acids) added to it, when a violent
effervescence will take place. When this has subsided, the whole should be
subjected to heat, brought nearly to the boiling point for six or eight hours.
The acid must now be carefully poured off, and the precipitate washed in a
large quantity of water, allowing some three or four hours between each
washing, for the subsidence of some of the lighter forms. The sediment
cover should come nearly, but not quite, to
the edge of the cell, a slight margin being
left for the cement, which should project
slightly over the edge of the cover, in order
to secure it to the cell.
Media for Preserving Algæ.—The most
Fig. 264.—Spring Clip for Mounting.
useful preservative media for algæ are
chrome-alum, formalin, and camphor water. The solution should consist of
one per cent. of chrome-alum and one per cent. of formalin; this will render
the gelatinous sheath and matrix form clear, while it will retain the colour of
the algæ in most cases. The Chlorophyceæ do well in any of these media;
but other species, as Ulva Lactuca, are rendered somewhat brittle. For such
use formalin alone. The Phæophyceæ should be placed while fresh in the
formalin; the larger forms are better fixed by placing them for an hour or
two in chrome-alum solution. The Florideæ do well in any of the three
solutions, but the more delicate species, Griffithsia, require a two per cent.
formalin solution in sea-water; the plant preserves its natural appearance in
this medium.
To preserve and mount diatomaceæ in as nearly as possible a natural
condition, they should be first well washed in distilled water and mounted
in a medium composed of one part of spirits of wine to seven parts of
distilled water. The siliceous coverings of the diatoms, however, which
show various beautiful forms under the higher powers of the microscope,
require more care in preparation. The guano, or infusorial earth containing
them, should first be washed several times in water till the water is
colourless, allowing sufficient time for precipitation between each washing.
The deposit must then be put into a test tube and nitro-hydrochloric acid
(equal parts of nitric and hydrochloric acids) added to it, when a violent
effervescence will take place. When this has subsided, the whole should be
subjected to heat, brought nearly to the boiling point for six or eight hours.
The acid must now be carefully poured off, and the precipitate washed in a
large quantity of water, allowing some three or four hours between each
washing, for the subsidence of some of the lighter forms. The sediment
Page 407
must be examined under the microscope with an inch object-glass, and the
siliceous valves of the diatoms picked out with a coarse hair or bristle.
Dr. Rezner’s Mechanical Finger (Fig. 265) for selecting and arranging
diatoms, adaptable to any microscope, is made to slip on to the objective far
enough to have a firm bearing, and so that the bristle point can be brought
into focus when depressed to its limit. It is clamped in its place by a small
thumb-screw. The bristle holder slides into its place, and is carefully
adjusted to the centre of the field. When using the finger, the bristle is first
raised by means of the micrometer screw till so far within focus as to be
nearly or quite invisible, then the objective is focussed on to the slide, and
the desired object sought for and brought into the centre of the field; the
bristle point is then lowered by the screw until it reaches the object, which
usually adheres to it at once, and can then be examined by rotating the
bristle wire by means of the milled head.
Fig. 265.—Rezner’s Mechanical Finger.
The medium used for mounting diatomaceæ is of considerable importance,
inasmuch as their visibility is either diminished or much increased thereby.
Professor Abbe, experimenting with the more minute test objects, diatoms,
&c., found monobromide of naphthaline gave increased definition to most
of them. This liquid is colourless, somewhat of an oleaginous nature, and is
soluble in alcohol. Its density is 1·555, and refractive index 1·6. Its index of
visibility is about twice that of Canada balsam.
Taking the refractive index of air as 1·0, and diatomaceous silex as 1·43,
the visibility may be expressed by the difference ·43.
siliceous valves of the diatoms picked out with a coarse hair or bristle.
Dr. Rezner’s Mechanical Finger (Fig. 265) for selecting and arranging
diatoms, adaptable to any microscope, is made to slip on to the objective far
enough to have a firm bearing, and so that the bristle point can be brought
into focus when depressed to its limit. It is clamped in its place by a small
thumb-screw. The bristle holder slides into its place, and is carefully
adjusted to the centre of the field. When using the finger, the bristle is first
raised by means of the micrometer screw till so far within focus as to be
nearly or quite invisible, then the objective is focussed on to the slide, and
the desired object sought for and brought into the centre of the field; the
bristle point is then lowered by the screw until it reaches the object, which
usually adheres to it at once, and can then be examined by rotating the
bristle wire by means of the milled head.
Fig. 265.—Rezner’s Mechanical Finger.
The medium used for mounting diatomaceæ is of considerable importance,
inasmuch as their visibility is either diminished or much increased thereby.
Professor Abbe, experimenting with the more minute test objects, diatoms,
&c., found monobromide of naphthaline gave increased definition to most
of them. This liquid is colourless, somewhat of an oleaginous nature, and is
soluble in alcohol. Its density is 1·555, and refractive index 1·6. Its index of
visibility is about twice that of Canada balsam.
Taking the refractive index of air as 1·0, and diatomaceous silex as 1·43,
the visibility may be expressed by the difference ·43.
Page 408
The following table may be constructed :—
Refractive indices Visibility of silex
(taken approximately). (Refr. index = 1·43).
Water .. = 1·33 .. 10
Canada balsam .. = 1·54 .. 11
Bisulphide of carbon .. = 1·68 .. 25
Sol. of sulphur in bisulph. .. = 1·75 .. 32
" phosphorus " .. = 2·11 .. 67
These data relating to visibility must be taken in connection with the
numerical aperture of the objectives and of the illuminating pencil. The
effect produced on diatoms is very remarkable, the markings on their
siliceous frustules being visible under much lower powers.
So that the visibility of the diatom mounted in phosphorus as compared
with balsam is as sixty-seven to eleven; in other words, the image is six
times more visible. Mr. Stephenson’s phosphorus medium is composed of a
solution of solid or stick phosphorous dissolved in bisulphide of carbon.
Great care is required in preparing the solution owing to the very
inflammable nature of the materials. So small a quantity of the bisulphide of
carbon is required to dissolve the phosphorus that the diatom may be said to
be mounted in nearly pure phosphorus. Remarkable enough, this medium
has the reverse effect upon such test-objects as podura and lepisma scales.
These lose their characteristic markings.
For mounting minute objects, carbolic acid solution will be found a useful
medium—the purest crystals of carbolic acid dissolved in just sufficient
water to render them fluid. No more should be dissolved than may be
wanted for the time being, as if left standing exposed to the light it changes
colour. Small crustacean foraminifera, the palates of moluscs, after boiling a
short time in liquid potash and well washing to remove all traces of alkali,
may be preserved in carbolic acid solution. Should the specimens appear
cloudy gently warm the slide over a spirit lamp.
Preserving and Killing Rotatoria with cilia in situ.—Mr. C. Rousselet’s
method of preserving and mounting the Rotatoria47 has been attended with
Refractive indices Visibility of silex
(taken approximately). (Refr. index = 1·43).
Water .. = 1·33 .. 10
Canada balsam .. = 1·54 .. 11
Bisulphide of carbon .. = 1·68 .. 25
Sol. of sulphur in bisulph. .. = 1·75 .. 32
" phosphorus " .. = 2·11 .. 67
These data relating to visibility must be taken in connection with the
numerical aperture of the objectives and of the illuminating pencil. The
effect produced on diatoms is very remarkable, the markings on their
siliceous frustules being visible under much lower powers.
So that the visibility of the diatom mounted in phosphorus as compared
with balsam is as sixty-seven to eleven; in other words, the image is six
times more visible. Mr. Stephenson’s phosphorus medium is composed of a
solution of solid or stick phosphorous dissolved in bisulphide of carbon.
Great care is required in preparing the solution owing to the very
inflammable nature of the materials. So small a quantity of the bisulphide of
carbon is required to dissolve the phosphorus that the diatom may be said to
be mounted in nearly pure phosphorus. Remarkable enough, this medium
has the reverse effect upon such test-objects as podura and lepisma scales.
These lose their characteristic markings.
For mounting minute objects, carbolic acid solution will be found a useful
medium—the purest crystals of carbolic acid dissolved in just sufficient
water to render them fluid. No more should be dissolved than may be
wanted for the time being, as if left standing exposed to the light it changes
colour. Small crustacean foraminifera, the palates of moluscs, after boiling a
short time in liquid potash and well washing to remove all traces of alkali,
may be preserved in carbolic acid solution. Should the specimens appear
cloudy gently warm the slide over a spirit lamp.
Preserving and Killing Rotatoria with cilia in situ.—Mr. C. Rousselet’s
method of preserving and mounting the Rotatoria47 has been attended with
Page 409
so much success that the old difficulty attendant upon the preservation of
these various beautiful forms of infusorial life has been practically
overcome. The process resorted to consists of four stages, namely,
narcotising, killing, fixing, and preserving. In dealing with rotifers hitherto,
the difficulty has been that of successfully killing them with their rotating
organs fully extended. It has been found needful to have recourse in the first
instance to a narcotising agent, and one that acts slowly. The most suitable
is a weak solution of the hydrochlorate of cocaine, a one per cent. solution,
or even weaker. This was first proposed by Mr. Weber for keeping these
active little bodies quiet while under observation. Mr. Rousselet carries this
agent further; he applied it to narcotise them prior to killing, and this it does
most effectually. The rotifers are seen to sink to the bottom of the live-cell,
and the cilia gradually to slacken in motion, and the time for killing has
arrived. This is effected by Flemming’s chromo-aceto-osmic acid. A rather
weak solution must be employed—consisting of 1 per cent. solution of
chromic acid, 15 parts; 2 per cent. osmic acid, 4 parts; glacial acetic acid, 1
part—which is at the same time a killing and fixing medium. The word
“fixing” must not be taken to imply simply fixing, as it includes rapidly
killing and hardening and preventing further change in the tissues of the
rotifers by subsequent treatment, as mounting. The animal, therefore, must
remain quietly for a few minutes, and then taken out and washed in five or
six changes of distilled water, and hence transferred to the preservative
fluid. All this must be effected with great care. The best preservative fluid is
simply distilled water, rendered antiseptic by a trace of the fixing solution
(about eight drops to an ounce of water) giving the slightest tinge of yellow
to the solution. This slight tinge of colour is imparted to the rotifers,
otherwise they remain transparent and unchanged, while the nervous tissue
throughout the body is brought out to perfection.
Some slight difference in treatment is required by certain species, as that of
Asplanchna priodonta; after the application of the cocaine solution, which
should be added slowly, that is, by letting a few drops trickle down the side
of the live-trough; this, being heavier than water, sinks to the bottom, thus
narcotising the rotifers, and assisting to kill them with the cilia fully
expanded. They should be left quietly for fifteen minutes, then thoroughly
washed with distilled water. On further experimenting, Mr. Rousselet found
that a weaker solution of osmic acid alone, ¼ per cent., answers quite as
these various beautiful forms of infusorial life has been practically
overcome. The process resorted to consists of four stages, namely,
narcotising, killing, fixing, and preserving. In dealing with rotifers hitherto,
the difficulty has been that of successfully killing them with their rotating
organs fully extended. It has been found needful to have recourse in the first
instance to a narcotising agent, and one that acts slowly. The most suitable
is a weak solution of the hydrochlorate of cocaine, a one per cent. solution,
or even weaker. This was first proposed by Mr. Weber for keeping these
active little bodies quiet while under observation. Mr. Rousselet carries this
agent further; he applied it to narcotise them prior to killing, and this it does
most effectually. The rotifers are seen to sink to the bottom of the live-cell,
and the cilia gradually to slacken in motion, and the time for killing has
arrived. This is effected by Flemming’s chromo-aceto-osmic acid. A rather
weak solution must be employed—consisting of 1 per cent. solution of
chromic acid, 15 parts; 2 per cent. osmic acid, 4 parts; glacial acetic acid, 1
part—which is at the same time a killing and fixing medium. The word
“fixing” must not be taken to imply simply fixing, as it includes rapidly
killing and hardening and preventing further change in the tissues of the
rotifers by subsequent treatment, as mounting. The animal, therefore, must
remain quietly for a few minutes, and then taken out and washed in five or
six changes of distilled water, and hence transferred to the preservative
fluid. All this must be effected with great care. The best preservative fluid is
simply distilled water, rendered antiseptic by a trace of the fixing solution
(about eight drops to an ounce of water) giving the slightest tinge of yellow
to the solution. This slight tinge of colour is imparted to the rotifers,
otherwise they remain transparent and unchanged, while the nervous tissue
throughout the body is brought out to perfection.
Some slight difference in treatment is required by certain species, as that of
Asplanchna priodonta; after the application of the cocaine solution, which
should be added slowly, that is, by letting a few drops trickle down the side
of the live-trough; this, being heavier than water, sinks to the bottom, thus
narcotising the rotifers, and assisting to kill them with the cilia fully
expanded. They should be left quietly for fifteen minutes, then thoroughly
washed with distilled water. On further experimenting, Mr. Rousselet found
that a weaker solution of osmic acid alone, ¼ per cent., answers quite as
Page 410
well as, if not better than, Flemming’s fluid; even this must be allowed to
act for only a very short time—a minute at most; the rotifers then remain
white and transparent, excepting the ova, in which a fat-like substance,
lecithene, is secreted. If they become too much stained, they may be
decolourised by passing them through peroxide of hydrogen. For
narcotising the following solution has been found most useful:—Take a 2
per cent. solution of cocaine hydrochlorate, 3 parts; methylated spirit of
wood naphtha, 1 part; and distilled water, 6 parts. This must be added as
before directed, drop by drop, watching the effect upon the rotifers under
the microscope.
All the rotatoria may be killed and preserved in the same way. For
mounting, Mr. Rousselet prefers a slightly hollowed-out glass cell, the
advantage of which is that the rotifers are kept to the centre, and cannot
move to the edge. A little difficulty at first presents itself to exclude air-
bubbles, but this, with a little care, can be overcome by placing a drop of a
two or three per cent. solution of formalin, just sufficient to fill the cell.
Then transfer the rotifers with a dipping pipette to the cell, and lower the
cover-glass down very gently, removing any excess of fluid by blotting-
paper. The best cement for the cover-glass is gold-size.
Method of Cementing.—After many years’ experience, I have arrived at the
conclusion that for cementing down the cover-glass there is nothing better
than either gold size or gum dammar varnish. The latter, for some
preparations, will be improved by the addition of a small proportion of
indiarubber dissolved in naphtha. (See Appendix.)
Should glycerine be preferred, carefully wash away any surplus quantity by
gently syringing; then apply a ring of waterproof cement round the cover-
glass. An inexpensive one can be made by dissolving ten grains of gum-
ammoniac in an ounce of acetic acid, and adding to this solution two
drachms of Cox’s gelatine. This liquid flows easily from the brush and is
waterproof, rendered more so if subsequently brushed over with a solution
of ten grains of bichromate of potash in an ounce of water. An especial
recommendation to this cement is its adhesiveness to glass, even should
there be a little glycerine left behind on the cover. After the gelatine ring is
thoroughly dry any kind of cement may be employed.
act for only a very short time—a minute at most; the rotifers then remain
white and transparent, excepting the ova, in which a fat-like substance,
lecithene, is secreted. If they become too much stained, they may be
decolourised by passing them through peroxide of hydrogen. For
narcotising the following solution has been found most useful:—Take a 2
per cent. solution of cocaine hydrochlorate, 3 parts; methylated spirit of
wood naphtha, 1 part; and distilled water, 6 parts. This must be added as
before directed, drop by drop, watching the effect upon the rotifers under
the microscope.
All the rotatoria may be killed and preserved in the same way. For
mounting, Mr. Rousselet prefers a slightly hollowed-out glass cell, the
advantage of which is that the rotifers are kept to the centre, and cannot
move to the edge. A little difficulty at first presents itself to exclude air-
bubbles, but this, with a little care, can be overcome by placing a drop of a
two or three per cent. solution of formalin, just sufficient to fill the cell.
Then transfer the rotifers with a dipping pipette to the cell, and lower the
cover-glass down very gently, removing any excess of fluid by blotting-
paper. The best cement for the cover-glass is gold-size.
Method of Cementing.—After many years’ experience, I have arrived at the
conclusion that for cementing down the cover-glass there is nothing better
than either gold size or gum dammar varnish. The latter, for some
preparations, will be improved by the addition of a small proportion of
indiarubber dissolved in naphtha. (See Appendix.)
Should glycerine be preferred, carefully wash away any surplus quantity by
gently syringing; then apply a ring of waterproof cement round the cover-
glass. An inexpensive one can be made by dissolving ten grains of gum-
ammoniac in an ounce of acetic acid, and adding to this solution two
drachms of Cox’s gelatine. This liquid flows easily from the brush and is
waterproof, rendered more so if subsequently brushed over with a solution
of ten grains of bichromate of potash in an ounce of water. An especial
recommendation to this cement is its adhesiveness to glass, even should
there be a little glycerine left behind on the cover. After the gelatine ring is
thoroughly dry any kind of cement may be employed.
Page 411
A useful cement for fixing minute objects, diatoms, &c., temporarily to thin
glass covers, before permanently mounting them in Canada balsam, is made
as follows:—Dissolve, without heat, two or three grains of gum arabic in
one ounce of distilled water, then add glacial acetic acid, three minims, and
the least trace of sugar. Filter carefully through filter paper, and repeat this
in the course of three or four weeks. This cement will be unaffected by the
balsam.
Mounting Chara.—It is often found difficult to preserve and mount the fruit
of chara, but this can be successfully accomplished in glycerine jelly, by
taking the following precautions. After cleaning the specimen place it in 92
per cent. of alcohol for several hours, then transfer it to a mixture of equal
parts of spirit and glycerine for several hours longer, pour off nearly all the
mixture, and add pure glycerine at intervals till the glycerine becomes
concentrated. The specimen is then mounted in glycerine jelly in a cell just
deep enough to take it without pressure.
There are some objects much more difficult to prepare than others, and
which tax the patience of the beginner in a manner which can hardly be
imagined by any one who has never made the attempt. The structure of
many creatures is so delicate as to require the very greatest care to prevent
mutilation, and consequent spoliation, of the specimen. The beginner,
therefore, must not be discouraged by a few failures in commencing, but
should persevere in his attempts, and constant practice will soon teach him
the best way of managing intricate and difficult objects. The room in which
he operates should be free from dust, smoke, and intrusion, and everything
used should be kept scrupulously clean, since a very small speck of dirt,
which may be almost invisible to the naked eye, will assume unpleasant
proportions under the microscope, and not only mar, but possibly spoil a
fine and delicate preparation.
Few students on commencing to work with the microscope will fully realise
the fact that under medium or high powers the natural appearance of almost
all objects is changed by the refractive nature of the fluid medium in which
they are immersed and which enters more or less into their composition.
The remarkable changes effected by the law of diffusion, when alkaloid
substances enter into their composition, show the necessity of taking every
glass covers, before permanently mounting them in Canada balsam, is made
as follows:—Dissolve, without heat, two or three grains of gum arabic in
one ounce of distilled water, then add glacial acetic acid, three minims, and
the least trace of sugar. Filter carefully through filter paper, and repeat this
in the course of three or four weeks. This cement will be unaffected by the
balsam.
Mounting Chara.—It is often found difficult to preserve and mount the fruit
of chara, but this can be successfully accomplished in glycerine jelly, by
taking the following precautions. After cleaning the specimen place it in 92
per cent. of alcohol for several hours, then transfer it to a mixture of equal
parts of spirit and glycerine for several hours longer, pour off nearly all the
mixture, and add pure glycerine at intervals till the glycerine becomes
concentrated. The specimen is then mounted in glycerine jelly in a cell just
deep enough to take it without pressure.
There are some objects much more difficult to prepare than others, and
which tax the patience of the beginner in a manner which can hardly be
imagined by any one who has never made the attempt. The structure of
many creatures is so delicate as to require the very greatest care to prevent
mutilation, and consequent spoliation, of the specimen. The beginner,
therefore, must not be discouraged by a few failures in commencing, but
should persevere in his attempts, and constant practice will soon teach him
the best way of managing intricate and difficult objects. The room in which
he operates should be free from dust, smoke, and intrusion, and everything
used should be kept scrupulously clean, since a very small speck of dirt,
which may be almost invisible to the naked eye, will assume unpleasant
proportions under the microscope, and not only mar, but possibly spoil a
fine and delicate preparation.
Few students on commencing to work with the microscope will fully realise
the fact that under medium or high powers the natural appearance of almost
all objects is changed by the refractive nature of the fluid medium in which
they are immersed and which enters more or less into their composition.
The remarkable changes effected by the law of diffusion, when alkaloid
substances enter into their composition, show the necessity of taking every
Page 412
precaution in the employment of preservative fluids. Glycerine affords an
example of the chemical change induced, should the preparation have been
passed through an alkaline solution.
Air Bubbles are a constant source of annoyance both in preparing and
mounting. These may be removed from the specimen by gently warming
the under part of the slide over a spirit lamp, or placing the slide in the
warm chamber, when the bubbles will move towards the edge of the cover-
glass and ultimately disappear. The air-pump is preferred by many
microscopists.
Collection of Objects.
Infusorial Life, with all its fascinations, was fully unveiled to naturalists by
the celebrated Ehrenberg. It was he who termed it infusorial, because he
first met with the more interesting forms of minute life in infusions of hay
and other vegetable substances. Since his day it is a well-known experience
of those who take up the microscope that the most interesting objects to
commence with are infusorial living creatures of sufficient dimensions to be
easily understood and seen with moderate magnifying powers. Moreover,
infusoria are more readily found in almost any pool or running stream of
water, either near the surface or clinging to the under surfaces of aquatic
plants. At one time all the small shallow pools in the neighbourhood of
London—Hampstead Heath, Clapham, Wandsworth, and other commons—
abounded in the most interesting forms of life, were famous hunting
grounds for the marvellous volvox, the charming dismid and diatom, the
wonderful budding and self-dividing hydra. A few hours’ ramble furnished
the microscopist with a bountiful supply of these and many other forms of
life. Now all is changed; our commons have been devoted to other
purposes, and with the general levelling up all the little pools have
disappeared, and the microscopist has been warned off and driven further
afield, or seeks the good offices of a country friend for an occasional peep
into pond life.48
A teaspoonful, however, judiciously taken from a well-chosen locality will
often be found to contain a variety of living forms, every one of which will
example of the chemical change induced, should the preparation have been
passed through an alkaline solution.
Air Bubbles are a constant source of annoyance both in preparing and
mounting. These may be removed from the specimen by gently warming
the under part of the slide over a spirit lamp, or placing the slide in the
warm chamber, when the bubbles will move towards the edge of the cover-
glass and ultimately disappear. The air-pump is preferred by many
microscopists.
Collection of Objects.
Infusorial Life, with all its fascinations, was fully unveiled to naturalists by
the celebrated Ehrenberg. It was he who termed it infusorial, because he
first met with the more interesting forms of minute life in infusions of hay
and other vegetable substances. Since his day it is a well-known experience
of those who take up the microscope that the most interesting objects to
commence with are infusorial living creatures of sufficient dimensions to be
easily understood and seen with moderate magnifying powers. Moreover,
infusoria are more readily found in almost any pool or running stream of
water, either near the surface or clinging to the under surfaces of aquatic
plants. At one time all the small shallow pools in the neighbourhood of
London—Hampstead Heath, Clapham, Wandsworth, and other commons—
abounded in the most interesting forms of life, were famous hunting
grounds for the marvellous volvox, the charming dismid and diatom, the
wonderful budding and self-dividing hydra. A few hours’ ramble furnished
the microscopist with a bountiful supply of these and many other forms of
life. Now all is changed; our commons have been devoted to other
purposes, and with the general levelling up all the little pools have
disappeared, and the microscopist has been warned off and driven further
afield, or seeks the good offices of a country friend for an occasional peep
into pond life.48
A teaspoonful, however, judiciously taken from a well-chosen locality will
often be found to contain a variety of living forms, every one of which will
Page 413
deserve a careful and patient study.
Of the microscopic organisms, the collection of which requires no other
methods than those ordinarily pursued by the naturalist, most of them must
be sought for in pools or running waters, basking in the sunshine, clinging
to leaves and rootlets of all aquatic plants; some freely moving about, others
clinging to stones or pieces of wood at the bottom. Dismids congregate in
shallow waters or rise to the surface in a quiet nook, while the diatomaceæ
are seen covering the bottom of clear water, to which they give a yellowish-
brown tinge of colour.
Infusorial animal life, as vorticellæ, stentors, rotifers, and various polyzoa,
cling, as also do hydra, in colonies to vallisneria, duck-weed, frogbit, or
small branches dipping down under water; and if some of the water-weed is
brought home the little creatures will live and thrive for several weeks. No
waters, however, are so full of minute animal life as the sphagnum bog. A
number of species of diatoms, as well as protozoids and the smaller
molluscs, will be found in all peat bogs. It is remarkable, too, that the same
species, everywhere, are associated with this kind of moss. Lord Sidney
Godolphin Osborn supplied his friends with moss growing in a damp part
of the garden walk of his rectory; this always furnished the same species of
rotifers. These proved to be most interesting objects to my friends, and in an
early communication I described them as indestructible, since they will bear
any amount of desiccation; nevertheless, they were revived when a drop of
water was introduced into the glass-cell.
Of the microscopic organisms, the collection of which requires no other
methods than those ordinarily pursued by the naturalist, most of them must
be sought for in pools or running waters, basking in the sunshine, clinging
to leaves and rootlets of all aquatic plants; some freely moving about, others
clinging to stones or pieces of wood at the bottom. Dismids congregate in
shallow waters or rise to the surface in a quiet nook, while the diatomaceæ
are seen covering the bottom of clear water, to which they give a yellowish-
brown tinge of colour.
Infusorial animal life, as vorticellæ, stentors, rotifers, and various polyzoa,
cling, as also do hydra, in colonies to vallisneria, duck-weed, frogbit, or
small branches dipping down under water; and if some of the water-weed is
brought home the little creatures will live and thrive for several weeks. No
waters, however, are so full of minute animal life as the sphagnum bog. A
number of species of diatoms, as well as protozoids and the smaller
molluscs, will be found in all peat bogs. It is remarkable, too, that the same
species, everywhere, are associated with this kind of moss. Lord Sidney
Godolphin Osborn supplied his friends with moss growing in a damp part
of the garden walk of his rectory; this always furnished the same species of
rotifers. These proved to be most interesting objects to my friends, and in an
early communication I described them as indestructible, since they will bear
any amount of desiccation; nevertheless, they were revived when a drop of
water was introduced into the glass-cell.
Page 414
Fig. 266.—Collecting Stick, Bottle, Hook, and Net.
The Thames mud always furnishes a number of beautiful forms of
triceratum. Lower down the river, as brackish water is reached, greater
varieties of diatoms appear. But to secure them the collector must be
provided with a collecting stick. A convenient form is furnished by Messrs.
Baker (Fig. 266). This consists of an ordinary walking-stick, together with a
lengthening rod, a cutting hook to clear away weeds, ringed bottles with
screw tops, and a net with a glass tube attached. Their uses are too obvious
to need further description.
The siliceous skeletons of diatoms are met with in the fossil state. Among
the first discovered of the infusorial strata were the polishing slates of Bilin
and Tripoli, the berg-mehl or mountain meal, the entire mass of which is
composed of the siliceous skeletons of different species of diatoms.
Richmond, Virginia, is rich in the same organisms, while the great mass of
our chalk cliffs are composed of foraminiferous shells, xanthidiæ, &c. One
remarkable fact in connection with fossil infusoria is that most of the forms
are still found in the recent state. The beautiful engine-turned discs,
Coscinodisci, so abundant in the Richmond earth, may be met with in our
own seas, and in great profusion in the deposits of guano on the African and
American coasts, and in the stomachs of the oyster, scallop, and other salt-
water molluscous animals common to our shores.
The Thames mud always furnishes a number of beautiful forms of
triceratum. Lower down the river, as brackish water is reached, greater
varieties of diatoms appear. But to secure them the collector must be
provided with a collecting stick. A convenient form is furnished by Messrs.
Baker (Fig. 266). This consists of an ordinary walking-stick, together with a
lengthening rod, a cutting hook to clear away weeds, ringed bottles with
screw tops, and a net with a glass tube attached. Their uses are too obvious
to need further description.
The siliceous skeletons of diatoms are met with in the fossil state. Among
the first discovered of the infusorial strata were the polishing slates of Bilin
and Tripoli, the berg-mehl or mountain meal, the entire mass of which is
composed of the siliceous skeletons of different species of diatoms.
Richmond, Virginia, is rich in the same organisms, while the great mass of
our chalk cliffs are composed of foraminiferous shells, xanthidiæ, &c. One
remarkable fact in connection with fossil infusoria is that most of the forms
are still found in the recent state. The beautiful engine-turned discs,
Coscinodisci, so abundant in the Richmond earth, may be met with in our
own seas, and in great profusion in the deposits of guano on the African and
American coasts, and in the stomachs of the oyster, scallop, and other salt-
water molluscous animals common to our shores.
Page 415
A great number of infusorial earths may be mounted as dry objects, while
others require careful washing and digesting in appropriate media. The finer
portions of the sediments will be found to contain the better and more
perfect siliceous shells.
Preparing and Mounting Apparatus.
Fig. 267.—Mounting Apparatus.
1.—Ross’s instrument for cutting thin covering-glass for objects. This apparatus
consists of a bent arm supporting the cutting portion of this apparatus, which
consists of a vertical rod with a soft cork at one end. A brass arm at right angles
carries the diamond parallel with and close to the main rod.
2.—Covering-glass measurer. To measure the thickness of covering-glass, place it
between the brass plate and the steel bearing; the long end of the lever will then
indicate the thickness on the scale, to 1⁄50-th, 1⁄100-th, or 1⁄1000-th inch.
3.—Brass table on folding legs, with lamp for mounting objects.
4.—Whirling table with eccentric adjustment for making cells and finishing off
slides.
5.—Air-pump with glass receiver, 3½-inch brass plate for mounting objects and
withdrawing air-bubbles.
6.—Improved table with knife for cutting soft sections. This consists of an
absolutely flat brass table, with a square hole to receive the wood, or other matter,
on a movable screw, which adjusts the thickness of the section.
7.—Smith’s holder with spring and screw for adjusting pressure when mounting
objects.
others require careful washing and digesting in appropriate media. The finer
portions of the sediments will be found to contain the better and more
perfect siliceous shells.
Preparing and Mounting Apparatus.
Fig. 267.—Mounting Apparatus.
1.—Ross’s instrument for cutting thin covering-glass for objects. This apparatus
consists of a bent arm supporting the cutting portion of this apparatus, which
consists of a vertical rod with a soft cork at one end. A brass arm at right angles
carries the diamond parallel with and close to the main rod.
2.—Covering-glass measurer. To measure the thickness of covering-glass, place it
between the brass plate and the steel bearing; the long end of the lever will then
indicate the thickness on the scale, to 1⁄50-th, 1⁄100-th, or 1⁄1000-th inch.
3.—Brass table on folding legs, with lamp for mounting objects.
4.—Whirling table with eccentric adjustment for making cells and finishing off
slides.
5.—Air-pump with glass receiver, 3½-inch brass plate for mounting objects and
withdrawing air-bubbles.
6.—Improved table with knife for cutting soft sections. This consists of an
absolutely flat brass table, with a square hole to receive the wood, or other matter,
on a movable screw, which adjusts the thickness of the section.
7.—Smith’s holder with spring and screw for adjusting pressure when mounting
objects.
Page 416
8.—Cutting diamonds for cell-making and cutting slips of glass.
9.—Writing diamonds for cutting thin covering-glass and naming objects.
10.—Page’s wooden forceps, for holding glass slips or objects when heated, during
mounting.
9.—Writing diamonds for cutting thin covering-glass and naming objects.
10.—Page’s wooden forceps, for holding glass slips or objects when heated, during
mounting.
Page 417
PART II.
Page 418
CHAPTER I.
Microscopic Forms of Life—Thallophytes—Pteridophyta,
Phanerogamæ—Structure and Properties of the Cell.
The time has long since passed by since the value of the microscope as an
instrument of scientific research might have been called in question. By its
aid the foundation of mycology has been securely laid, and cryptogamic
botany in particular has, during the last quarter of a century, made
surprising progress in the hands of those devoted to pursuits which confer
benefits upon mankind.
Little more than thirty years ago practically nothing was known of the life
history of a fungus, nothing of parasitism, of infectious diseases, or even of
fermentation. Our knowledge of the physiology of nutrition was in its
infancy; even the significance of starches and sugars in the green plant was
as yet not understood, while a number of the most important facts relating
to plants and the physiology of animals were unknown and undiscovered.
When we reflect on these matters, and remember that bacteria were
regarded merely as curious animalculæ, that rusts and smuts were supposed
to be emanations of diseased states, and that spontaneous generation still-
survived among us, some idea may be formed of the condition of
cryptogamic botany and the lower forms of animal life some eight or ten
years after my book on the microscope made its first appearance (1854).
Indeed, long prior to this time, dating from that of even the earliest workers
with the microscope, it was known that the water of pools and ditches, and
especially infusions of plants and animals of all kinds, teem with living
organisms, but it was not recognised definitely that vast numbers of these
microscopic living beings (and even actively moving ones) are plants,
Microscopic Forms of Life—Thallophytes—Pteridophyta,
Phanerogamæ—Structure and Properties of the Cell.
The time has long since passed by since the value of the microscope as an
instrument of scientific research might have been called in question. By its
aid the foundation of mycology has been securely laid, and cryptogamic
botany in particular has, during the last quarter of a century, made
surprising progress in the hands of those devoted to pursuits which confer
benefits upon mankind.
Little more than thirty years ago practically nothing was known of the life
history of a fungus, nothing of parasitism, of infectious diseases, or even of
fermentation. Our knowledge of the physiology of nutrition was in its
infancy; even the significance of starches and sugars in the green plant was
as yet not understood, while a number of the most important facts relating
to plants and the physiology of animals were unknown and undiscovered.
When we reflect on these matters, and remember that bacteria were
regarded merely as curious animalculæ, that rusts and smuts were supposed
to be emanations of diseased states, and that spontaneous generation still-
survived among us, some idea may be formed of the condition of
cryptogamic botany and the lower forms of animal life some eight or ten
years after my book on the microscope made its first appearance (1854).
Indeed, long prior to this time, dating from that of even the earliest workers
with the microscope, it was known that the water of pools and ditches, and
especially infusions of plants and animals of all kinds, teem with living
organisms, but it was not recognised definitely that vast numbers of these
microscopic living beings (and even actively moving ones) are plants,
Page 419
growing on and in the various solid and liquid matters examined, and as
truly as visible and accepted plants grow on soil and in the air and water.
Perhaps the most important discovery in the history of cryptogamic botany
was initiated here. The change, then, that has come over our knowledge of
microscopic plant life during this last busy quarter of a century has been
almost entirely due to the initiation and improvement, first in methods of
growing them, and in the methods of “Microscopic Gardening”; and
secondly, to the greater knowledge gained in the use of the microscope.
“If we look at the great groups of plants from a broad point of view, it is
remarkable that the fungi and the phanerogams occupy attention on quite
other grounds than do the algæ, mosses, and ferns. Algæ are especially a
physiologist’s group, employed in questions on nutrition, reproduction, and
cell division and growth; the Bryophyta and Pteridophyta are, on the other
hand, the domain of the morphologist. Fungi and Phanerogams, while
equally or even more employed by specialists in morphology and
physiology, appeal widely to general interest on the ground of utility.
“It is very significant that a group like the fungi should have attracted so
much scientific attention, and aroused so general an interest at the same
time. But the fact that fungi affect our lives directly has been driven home;
and whether as poisons or foods, destructive moulds or fermentation agents,
parasitic mildews or disease germs, they occupy more interest than all other
cryptogams put together, the flowering plants alone rivalling them in this
respect. A marked feature of the period in which we live will be the great
advances made in our knowledge of the uses of plants, for, of course, this
development of economic botany has gone hand in hand with the progress
of geological botany, the extension of our planting, and the useful
applications of botany to the processes of home industries.”49
The intimate organic structure of the vegetable world is seen to consist of a
variety of different materials indeterminable by unassisted vision, and for
the most part requiring high magnification for their discrimination.
Chemical analysis had, however, shown that vegetables are composed of a
few simple substances, water, carbonic acid gas, oxygen, nitric acid, and a
small portion of inorganic salts. Out of these simple elements the whole of
the immense variety of substances produced by the vegetable kingdom are
truly as visible and accepted plants grow on soil and in the air and water.
Perhaps the most important discovery in the history of cryptogamic botany
was initiated here. The change, then, that has come over our knowledge of
microscopic plant life during this last busy quarter of a century has been
almost entirely due to the initiation and improvement, first in methods of
growing them, and in the methods of “Microscopic Gardening”; and
secondly, to the greater knowledge gained in the use of the microscope.
“If we look at the great groups of plants from a broad point of view, it is
remarkable that the fungi and the phanerogams occupy attention on quite
other grounds than do the algæ, mosses, and ferns. Algæ are especially a
physiologist’s group, employed in questions on nutrition, reproduction, and
cell division and growth; the Bryophyta and Pteridophyta are, on the other
hand, the domain of the morphologist. Fungi and Phanerogams, while
equally or even more employed by specialists in morphology and
physiology, appeal widely to general interest on the ground of utility.
“It is very significant that a group like the fungi should have attracted so
much scientific attention, and aroused so general an interest at the same
time. But the fact that fungi affect our lives directly has been driven home;
and whether as poisons or foods, destructive moulds or fermentation agents,
parasitic mildews or disease germs, they occupy more interest than all other
cryptogams put together, the flowering plants alone rivalling them in this
respect. A marked feature of the period in which we live will be the great
advances made in our knowledge of the uses of plants, for, of course, this
development of economic botany has gone hand in hand with the progress
of geological botany, the extension of our planting, and the useful
applications of botany to the processes of home industries.”49
The intimate organic structure of the vegetable world is seen to consist of a
variety of different materials indeterminable by unassisted vision, and for
the most part requiring high magnification for their discrimination.
Chemical analysis had, however, shown that vegetables are composed of a
few simple substances, water, carbonic acid gas, oxygen, nitric acid, and a
small portion of inorganic salts. Out of these simple elements the whole of
the immense variety of substances produced by the vegetable kingdom are
Page 420
constructed. No part of the plant contains fewer than three of these
universally distributed elements, hence the greater uniformity in their
chemical constituents. It will be seen, then, that the methods of plant
chemistry are of supreme interest both to the chemist and the physiologist,
or biologist. Plants, while they borrow materials from the inorganic, and
powers from the physical world, whereby they are enabled to pass through
the several stages of germination, growth, and reproduction, could not
accomplish these transformations without the all-important aid of light and
heat, the combined functions of which are indispensable to the perfect
development of the vegetable world.
Light, then, enables plants to decompose, change into living matter, and
consolidate, the inorganic elements of carbonic acid gas, water, and
ammonia, which are absorbed by the leaves and roots from the atmosphere
and earth; the quantity of carbon consolidated being exactly in proportion to
the intensity of the light. Nevertheless, light in its chemical character is a
deoxidising agent, by which the numerous neutral compounds common to
vegetables are formed. It is the principal agent in preparing the food of
plants, and it is during the chemical changes spoken of that the specific heat
of plants is slowly evolved, which, though generally feeble, is sometimes
very sensibly evolved, especially so when flowers and fruits are forming, on
account of the increase of chemical energy at this period.
The action of heat is measurable throughout the whole course of vegetable
life, although its manifestations take on various forms—those suited to the
period and circumstances of growth. Upon the heat generated depends the
formation of protein and nitrogenous substances, which abound more
directly in the seed buds, the points of the roots, and in all those organs of
plants which are in the greatest state of activity. The whole chemistry of
plant life, in fact, is manifest in this production of energy for drawing
material from its surroundings; therefore the organising power of plants
bears a direct ratio to the amount of light and heat acting upon them.
The living medium, then, which possesses the marvellous property of being
primarily aroused into life and energy, and which either forms the whole or
the greater portion of every plant, is in its earliest and simplest form nothing
more than a microscopic cell, consisting of one or two colourless particles
universally distributed elements, hence the greater uniformity in their
chemical constituents. It will be seen, then, that the methods of plant
chemistry are of supreme interest both to the chemist and the physiologist,
or biologist. Plants, while they borrow materials from the inorganic, and
powers from the physical world, whereby they are enabled to pass through
the several stages of germination, growth, and reproduction, could not
accomplish these transformations without the all-important aid of light and
heat, the combined functions of which are indispensable to the perfect
development of the vegetable world.
Light, then, enables plants to decompose, change into living matter, and
consolidate, the inorganic elements of carbonic acid gas, water, and
ammonia, which are absorbed by the leaves and roots from the atmosphere
and earth; the quantity of carbon consolidated being exactly in proportion to
the intensity of the light. Nevertheless, light in its chemical character is a
deoxidising agent, by which the numerous neutral compounds common to
vegetables are formed. It is the principal agent in preparing the food of
plants, and it is during the chemical changes spoken of that the specific heat
of plants is slowly evolved, which, though generally feeble, is sometimes
very sensibly evolved, especially so when flowers and fruits are forming, on
account of the increase of chemical energy at this period.
The action of heat is measurable throughout the whole course of vegetable
life, although its manifestations take on various forms—those suited to the
period and circumstances of growth. Upon the heat generated depends the
formation of protein and nitrogenous substances, which abound more
directly in the seed buds, the points of the roots, and in all those organs of
plants which are in the greatest state of activity. The whole chemistry of
plant life, in fact, is manifest in this production of energy for drawing
material from its surroundings; therefore the organising power of plants
bears a direct ratio to the amount of light and heat acting upon them.
The living medium, then, which possesses the marvellous property of being
primarily aroused into life and energy, and which either forms the whole or
the greater portion of every plant, is in its earliest and simplest form nothing
more than a microscopic cell, consisting of one or two colourless particles
Page 421
of matter, in closest contact, and wholly immersed in a transparent
substance somewhat resembling albumen (white of egg), termed
protoplasm, but differing essentially in its character and properties. This
nearly colourless organisable matter is the life-blood of the cell. It is
sufficiently viscid to maintain its globular form, and under high powers is
seen to have a slightly consolidated film enclosing semi-transparent
particles, together with vacuoles which are of a highly refractive nature.
These small bodies are termed nuclei, and they appear to be furnished with
an extremely delicate enveloping film. In a short time the nuclei increase in
number and split up the parent body. The protoplasmic mass, however, is
undoubtedly the true formative material, and is rightly regarded as “the
physical basis of life” of both the vegetable and animal kingdoms.
There are, however, certain members of the vegetable kingdom which
somewhat resemble animals in their dependence upon receiving organic
compounds already formed for them, being themselves unable to effect the
fixation of the carbon needed to effect the first stage in their after chemical
transformations. Such is the case with a large class of flowering plants,
among Phanerogams, and the leafless parasites which draw their support
chiefly from the tissues of their hosts. It is likewise the case with regard to
the whole group of fungi; the lower cryptogams, which derive the greater
portion of their nutritive materials from organic matter undergoing some
form of histolysis; while others belonging to this group have the power of
originating decomposition by a fermentative (zymotic) action peculiarly
their own. There are many other protophytes which live by absorption, and
which appear to take in no solid matter, but draw nourishment from the
atmosphere or the water in which they exist.
With regard to motion, this was at one time considered the distinctive
attribute of animal life, but many protophytes possess a spontaneity of
power and motion, while others are furnished with curious motile organs
termed cilia, or whip-like appendages, flagella, by which their bodies are
propelled with considerable force through the water in which they live.
Henceforth this protoplasmic substance was destined to take an important
position in the physiological world. It is, then, desirable to enter somewhat
more fully into the life history of so remarkable a body. It has a limiting
substance somewhat resembling albumen (white of egg), termed
protoplasm, but differing essentially in its character and properties. This
nearly colourless organisable matter is the life-blood of the cell. It is
sufficiently viscid to maintain its globular form, and under high powers is
seen to have a slightly consolidated film enclosing semi-transparent
particles, together with vacuoles which are of a highly refractive nature.
These small bodies are termed nuclei, and they appear to be furnished with
an extremely delicate enveloping film. In a short time the nuclei increase in
number and split up the parent body. The protoplasmic mass, however, is
undoubtedly the true formative material, and is rightly regarded as “the
physical basis of life” of both the vegetable and animal kingdoms.
There are, however, certain members of the vegetable kingdom which
somewhat resemble animals in their dependence upon receiving organic
compounds already formed for them, being themselves unable to effect the
fixation of the carbon needed to effect the first stage in their after chemical
transformations. Such is the case with a large class of flowering plants,
among Phanerogams, and the leafless parasites which draw their support
chiefly from the tissues of their hosts. It is likewise the case with regard to
the whole group of fungi; the lower cryptogams, which derive the greater
portion of their nutritive materials from organic matter undergoing some
form of histolysis; while others belonging to this group have the power of
originating decomposition by a fermentative (zymotic) action peculiarly
their own. There are many other protophytes which live by absorption, and
which appear to take in no solid matter, but draw nourishment from the
atmosphere or the water in which they exist.
With regard to motion, this was at one time considered the distinctive
attribute of animal life, but many protophytes possess a spontaneity of
power and motion, while others are furnished with curious motile organs
termed cilia, or whip-like appendages, flagella, by which their bodies are
propelled with considerable force through the water in which they live.
Henceforth this protoplasmic substance was destined to take an important
position in the physiological world. It is, then, desirable to enter somewhat
more fully into the life history of so remarkable a body. It has a limiting
Page 422
membrane, composed of a substance somewhat allied to starch, termed
cellulose, one of the group of compounds known as carbo-hydrates. The
mode of formation and growth of this cell wall is not yet definitely
determined; nevertheless, it is the universal framework or skeleton of the
vegetable world, although it appears to play no special part in their vital
functions. It merely serves the purpose of a protecting membrane to the
globular body called the “primordial cell,” which permanently constitutes
the living principle upon which the whole fundamental phenomena of
growth and reproduction depend.
Sometimes this protoplasmic material is seen to constitute the whole plant;
and so with regard to the simplest known forms of animal life—the amœba,
for example. That so simple and minute an organism should be capable of
independent motion is indeed surprising. Dujardin, a French physiologist,
termed this animated matter sarcode. On a closer study of the numerous
forms of animal life it was found that all were alike composed of this
sarcode substance, some apparently not having a cell wall. The same
seemed to hold good of certain higher forms of cells, the colourless blood
corpuscles for instance, which under high powers of the microscope are
seen to change their shape, moving about by the streaming out of this
sarcode. At length the truth dawned on histologists that the cell contents,
rather than the closing wall, must be the essential structure. On further
investigation it became apparent that a far closer similarity existed between
vegetables and animals than was before supposed. Ultimately it was made
clear that the vegetable protoplasm and the animal sarcode were one and the
same structure. Max Schultz found this to be the case, and to all intents and
purposes they are identical.
We have now to retrace our steps and look somewhat more closely into the
discovery of that important body, the cell-nucleus. It was an English
botanist, Dr. Robert Brown, who, in 1833, during his microscopical studies
of the epidermis of orchids, discovered in their cells “an opaque spot,” to
which soon afterwards he gave the name of nucleus. Schleiden and
Schwann’s later researches led them to the conclusion that the nucleus is the
most characteristic formative element in all vegetable and animal tissues in
the incipient phase of existence. It then began to be taught that there is one
universal principle of development for the elementary parts of all
cellulose, one of the group of compounds known as carbo-hydrates. The
mode of formation and growth of this cell wall is not yet definitely
determined; nevertheless, it is the universal framework or skeleton of the
vegetable world, although it appears to play no special part in their vital
functions. It merely serves the purpose of a protecting membrane to the
globular body called the “primordial cell,” which permanently constitutes
the living principle upon which the whole fundamental phenomena of
growth and reproduction depend.
Sometimes this protoplasmic material is seen to constitute the whole plant;
and so with regard to the simplest known forms of animal life—the amœba,
for example. That so simple and minute an organism should be capable of
independent motion is indeed surprising. Dujardin, a French physiologist,
termed this animated matter sarcode. On a closer study of the numerous
forms of animal life it was found that all were alike composed of this
sarcode substance, some apparently not having a cell wall. The same
seemed to hold good of certain higher forms of cells, the colourless blood
corpuscles for instance, which under high powers of the microscope are
seen to change their shape, moving about by the streaming out of this
sarcode. At length the truth dawned on histologists that the cell contents,
rather than the closing wall, must be the essential structure. On further
investigation it became apparent that a far closer similarity existed between
vegetables and animals than was before supposed. Ultimately it was made
clear that the vegetable protoplasm and the animal sarcode were one and the
same structure. Max Schultz found this to be the case, and to all intents and
purposes they are identical.
We have now to retrace our steps and look somewhat more closely into the
discovery of that important body, the cell-nucleus. It was an English
botanist, Dr. Robert Brown, who, in 1833, during his microscopical studies
of the epidermis of orchids, discovered in their cells “an opaque spot,” to
which soon afterwards he gave the name of nucleus. Schleiden and
Schwann’s later researches led them to the conclusion that the nucleus is the
most characteristic formative element in all vegetable and animal tissues in
the incipient phase of existence. It then began to be taught that there is one
universal principle of development for the elementary parts of all
Page 423
organisms, however different, and that is the formation of cells. Thus was
enunciated a doctrine which was for all practical purposes absolutely new,
and which opened out a wide field of further investigation for the
physiologist, and led up to a fuller knowledge of the cell contents. In fact, it
became a question as to whether the cell contents rather than the enclosing
wall should not be considered the basis of life, since the cell at this time had
by no means lost its importance, although it no longer signified the minute
cavity it did when originally discovered by Schwann. It now implied, as
Schultz defined it, “a small mass of viscid matter, protoplasm, endowed
with the attributes of life.” The nucleus was once more restored to its
original importance, and with even greater significance. In place of being a
structure generated de novo from non-cellular substance, and disappearing
as soon as its function of cell formation is accomplished, the nucleus is now
known as the central permanent feature of every cell, and indestructible
while the cell lives, and the parent, by division of its substance, of other
generations of nuclei and cells. The word cell has at the same time received
its final definition as “a small mass of protoplasm supplied with a nucleus.”
In short, all the activities of plant and animal life are really the product of
energy liberated solely through histolysis, or destructive processes,
amounting to the combustion that takes place in the ultimate cells of the
organisms.
But there are other points of especial interest involved in the question of
cell formation beside those already mentioned.
The cell and its contents collectively are termed the endoplasm, or when
coloured, as in algæ, endochrome. With regard to the outer layer of the cell
and its growth nothing satisfactory has been clearly determined and finally
accepted.
The cell as a whole is a protoplasmic mass, and not an emulsion, as some
observers would have us suppose. It is, in fact, a reticulated tissue of the
most delicate structure, made up of canaliculate spiral fibrils with hyaline
walls capable of expansion and contraction. These fibrils are probably
composed of still finer spirals. The visible granulated portion of the
protoplasm, the only part that takes a stain under ordinary circumstances, is
simply the contents of these canals. It is the chromatin of Flemming, and is
enunciated a doctrine which was for all practical purposes absolutely new,
and which opened out a wide field of further investigation for the
physiologist, and led up to a fuller knowledge of the cell contents. In fact, it
became a question as to whether the cell contents rather than the enclosing
wall should not be considered the basis of life, since the cell at this time had
by no means lost its importance, although it no longer signified the minute
cavity it did when originally discovered by Schwann. It now implied, as
Schultz defined it, “a small mass of viscid matter, protoplasm, endowed
with the attributes of life.” The nucleus was once more restored to its
original importance, and with even greater significance. In place of being a
structure generated de novo from non-cellular substance, and disappearing
as soon as its function of cell formation is accomplished, the nucleus is now
known as the central permanent feature of every cell, and indestructible
while the cell lives, and the parent, by division of its substance, of other
generations of nuclei and cells. The word cell has at the same time received
its final definition as “a small mass of protoplasm supplied with a nucleus.”
In short, all the activities of plant and animal life are really the product of
energy liberated solely through histolysis, or destructive processes,
amounting to the combustion that takes place in the ultimate cells of the
organisms.
But there are other points of especial interest involved in the question of
cell formation beside those already mentioned.
The cell and its contents collectively are termed the endoplasm, or when
coloured, as in algæ, endochrome. With regard to the outer layer of the cell
and its growth nothing satisfactory has been clearly determined and finally
accepted.
The cell as a whole is a protoplasmic mass, and not an emulsion, as some
observers would have us suppose. It is, in fact, a reticulated tissue of the
most delicate structure, made up of canaliculate spiral fibrils with hyaline
walls capable of expansion and contraction. These fibrils are probably
composed of still finer spirals. The visible granulated portion of the
protoplasm, the only part that takes a stain under ordinary circumstances, is
simply the contents of these canals. It is the chromatin of Flemming, and is
Page 424
capable of motion within the canals. The nucleus, then, is probably nothing
more than a granule of the extra-cellular net, and is formed by the junction
of the several bands of wall-threads which traverse it in different directions.
The cell wall of plants possesses the same structure as protoplasm, and is
probably protoplasm impregnated by cellulose.
It is this portion of the protoplasmic mass that is now recognised under the
term octoplasm, or primordial utricle, and is of so fine and delicate a nature
that it is only brought into view when separated from the cell wall either by
further developmental changes, or by reagents and certain stains or dyes. It
was, in fact, discovered to be a slightly condensed portion of the
protoplasmic layer corresponding to the octosare of the lower forms of
animal life. The octoplasm and cell wall can only be distinguished from
each other by chemical tests. Both nucleus and nucleoli are only rendered
visible in the same way, that is, by staining for several hours in a carmine
solution, and washing in a weak acetic acid solution.
With the enlargement of the cell by the imbibition of water, clear spaces,
termed vacuoles, are seen to occupy a small portion of the cell, while the
nucleus and nucleoli lie close to the parietal layer.
The interesting phenomenon of cyclosis, to which I shall have occasion to
refer further on, is now believed to be due to the contractility of certain
wall-threads stretching from the nucleus to the outermost layers of the cell.
An intimate relationship is thereby established between the nucleus, the
nucleolus, and the parietal layer. This much has been made clear by the
more scientific methods of investigation pursued in the use of the
microscope. Nevertheless a large and important class of cells, forming a
kind of borderland between the vegetable and animal kingdoms, still
remains to be dealt with, in which the cell contents are only imperfectly
differentiated, while numerous other unicellular organisms, owing to their
extreme minuteness, tenuity, and want of all colour, are apparently devoid
of any nucleus, and when present can only be differentiated by a resort to a
specially conducted method of preparation and staining. There is, however,
a remarkable feature in connection with many micro-organisms—that
certain of these protophytes possess motive organs, cilia or flagella, bodies
at one time supposed to be characteristic of, and belonging to, the protozoa.
more than a granule of the extra-cellular net, and is formed by the junction
of the several bands of wall-threads which traverse it in different directions.
The cell wall of plants possesses the same structure as protoplasm, and is
probably protoplasm impregnated by cellulose.
It is this portion of the protoplasmic mass that is now recognised under the
term octoplasm, or primordial utricle, and is of so fine and delicate a nature
that it is only brought into view when separated from the cell wall either by
further developmental changes, or by reagents and certain stains or dyes. It
was, in fact, discovered to be a slightly condensed portion of the
protoplasmic layer corresponding to the octosare of the lower forms of
animal life. The octoplasm and cell wall can only be distinguished from
each other by chemical tests. Both nucleus and nucleoli are only rendered
visible in the same way, that is, by staining for several hours in a carmine
solution, and washing in a weak acetic acid solution.
With the enlargement of the cell by the imbibition of water, clear spaces,
termed vacuoles, are seen to occupy a small portion of the cell, while the
nucleus and nucleoli lie close to the parietal layer.
The interesting phenomenon of cyclosis, to which I shall have occasion to
refer further on, is now believed to be due to the contractility of certain
wall-threads stretching from the nucleus to the outermost layers of the cell.
An intimate relationship is thereby established between the nucleus, the
nucleolus, and the parietal layer. This much has been made clear by the
more scientific methods of investigation pursued in the use of the
microscope. Nevertheless a large and important class of cells, forming a
kind of borderland between the vegetable and animal kingdoms, still
remains to be dealt with, in which the cell contents are only imperfectly
differentiated, while numerous other unicellular organisms, owing to their
extreme minuteness, tenuity, and want of all colour, are apparently devoid
of any nucleus, and when present can only be differentiated by a resort to a
specially conducted method of preparation and staining. There is, however,
a remarkable feature in connection with many micro-organisms—that
certain of these protophytes possess motive organs, cilia or flagella, bodies
at one time supposed to be characteristic of, and belonging to, the protozoa.
Page 425
This being the case, the methods of plant chemistry are of supreme interest,
the more so because physiologists are in a position to isolate a single
bacterial cell, grow it in certain media, and thus devote special attention to
it, and keep it for some time under observation. In this way it has become
possible to further grasp facts in connection with cell nutrition and the
nature of its waste products. We have, then, arrived at a stage when the
history of the chemical changes brought about by bacteria can be more
definitely determined, as we have here to do with the vegetable cell in its
simplest form. The chemical work performed by these micro-organisms has
as yet occupied only a few years; nevertheless, the results have been of the
most remarkable and encouraging character.
At an earlier period an interesting discovery in connection with the
pathogenic action of these bodies was, by the labours of Schöenlein, Robin,
and others, brought to the notice of the medical profession, viz., that certain
diseases affecting the human body were due to vegetable parasites. In 1856
an opportunity offered itself for a thorough investigation, and the
microscopical part of the work fell into my hands, with the result that I was
able to add considerably to Schöenlein’s list of parasitic skin diseases. My
observations were in the first instance communicated to the medical
journals. But the generalisation arrived at was that “If there be any
exceptions to the law that parasites select for their sustenance the subjects
of debility and decay, such exceptions are rarely to be found among the
vegetations belonging to fungi, which invariably derive nutrition from
matter in a state of lowered vitality, passing into degeneration, or wherein
decomposition has already taken place to a certain extent.... It scarcely
admits of a doubt that all diseases observed of late years among plants have
been due to parasites of the same class favoured by want of vigour of
growth and atmospheric conditions, and that the cause of the various
murrains of which so much has been heard is also due to similar causes.”50
Herein, then, is to be found the solution of a difficulty that so long
surrounded the question, but which subsequently culminated in the
specialisation and scientific development of bacteriology, due to the
unceasing labours of Pasteur, whose solid genius enabled him to overcome
the prejudices of those who were at work on other lines, and who had no
conception of the functions that parasitic organisms fulfil in nature.
the more so because physiologists are in a position to isolate a single
bacterial cell, grow it in certain media, and thus devote special attention to
it, and keep it for some time under observation. In this way it has become
possible to further grasp facts in connection with cell nutrition and the
nature of its waste products. We have, then, arrived at a stage when the
history of the chemical changes brought about by bacteria can be more
definitely determined, as we have here to do with the vegetable cell in its
simplest form. The chemical work performed by these micro-organisms has
as yet occupied only a few years; nevertheless, the results have been of the
most remarkable and encouraging character.
At an earlier period an interesting discovery in connection with the
pathogenic action of these bodies was, by the labours of Schöenlein, Robin,
and others, brought to the notice of the medical profession, viz., that certain
diseases affecting the human body were due to vegetable parasites. In 1856
an opportunity offered itself for a thorough investigation, and the
microscopical part of the work fell into my hands, with the result that I was
able to add considerably to Schöenlein’s list of parasitic skin diseases. My
observations were in the first instance communicated to the medical
journals. But the generalisation arrived at was that “If there be any
exceptions to the law that parasites select for their sustenance the subjects
of debility and decay, such exceptions are rarely to be found among the
vegetations belonging to fungi, which invariably derive nutrition from
matter in a state of lowered vitality, passing into degeneration, or wherein
decomposition has already taken place to a certain extent.... It scarcely
admits of a doubt that all diseases observed of late years among plants have
been due to parasites of the same class favoured by want of vigour of
growth and atmospheric conditions, and that the cause of the various
murrains of which so much has been heard is also due to similar causes.”50
Herein, then, is to be found the solution of a difficulty that so long
surrounded the question, but which subsequently culminated in the
specialisation and scientific development of bacteriology, due to the
unceasing labours of Pasteur, whose solid genius enabled him to overcome
the prejudices of those who were at work on other lines, and who had no
conception of the functions that parasitic organisms fulfil in nature.
Page 426
Going back to my earlier experimental researches to determine the part
taken by saccharomycetes and saprophytes in fermentation, I find, from
correspondence in my possession, that in 1859 I demonstrated to the
satisfaction of Dr. Bell, F.R.S., the then head of the chemical laboratory of
Somerset House, that a very small portion of putrefactive matter taken from
an animal body, a parasitic fungus (Achorion Schöenleinii), a mould
(Aspergillus or Penicillium), and a yeast (Torula cerevisiæ) would in a short
time, and indifferently, set up a ferment in sweet-wort and transform its
saccharine elements into alcohol, differing only in degree (quantitative),
and not in kind or quality. This, then, was the first step in the direction
towards proving symbiotic action between these several parasitic
organisms. The only apparent difference observed during the fermentative
processes was that putrefactive (saprophytic) action commenced at a
somewhat earlier stage, and that the percentage of alcohol was also
somewhat less.51
In 1856, also, the ærobic bacteria attracted my attention, and, together with
the late Rev. Lord Sidney Godolphin Osborne, I exposed plates of glass
(microscopical slides), covered with glycerine and grape sugar, in every
conceivable place where we thought it possible to arrest micro-organisms.
The result is known, viz., that fungoid bodies (moulds and bacterial) were
taken in great numbers, and varying with the seasons. The air of the hospital
and sick-room likewise engaged attention, each of which proved especially
rich in parasitic bodies. During the cholera visitation of 1858 the air was
rich in ærobic and anærobic bacteria, while a blue mist which prevailed
throughout the epidemic yielded a far greater number than at any former
period (represented in Plate I., No. 13). This blue mist attracted the especial
attention of meteorologists. At a somewhat later period a more remarkable
fungoid disease, the fungus foot of India, mycetoma, came under my
observation, a detailed description of which I contributed to the medical
journals, and also, with further details, to the “Monthly Microscopical
Journal” of 1871. Interlacing mycelia, ending in hyphæ, in this destructive
form of parasitic disease were seen to pervade the whole of the tissues of
the foot, the bony structures being involved, and it was only possible to stay
the action of the parasite by amputation.
taken by saccharomycetes and saprophytes in fermentation, I find, from
correspondence in my possession, that in 1859 I demonstrated to the
satisfaction of Dr. Bell, F.R.S., the then head of the chemical laboratory of
Somerset House, that a very small portion of putrefactive matter taken from
an animal body, a parasitic fungus (Achorion Schöenleinii), a mould
(Aspergillus or Penicillium), and a yeast (Torula cerevisiæ) would in a short
time, and indifferently, set up a ferment in sweet-wort and transform its
saccharine elements into alcohol, differing only in degree (quantitative),
and not in kind or quality. This, then, was the first step in the direction
towards proving symbiotic action between these several parasitic
organisms. The only apparent difference observed during the fermentative
processes was that putrefactive (saprophytic) action commenced at a
somewhat earlier stage, and that the percentage of alcohol was also
somewhat less.51
In 1856, also, the ærobic bacteria attracted my attention, and, together with
the late Rev. Lord Sidney Godolphin Osborne, I exposed plates of glass
(microscopical slides), covered with glycerine and grape sugar, in every
conceivable place where we thought it possible to arrest micro-organisms.
The result is known, viz., that fungoid bodies (moulds and bacterial) were
taken in great numbers, and varying with the seasons. The air of the hospital
and sick-room likewise engaged attention, each of which proved especially
rich in parasitic bodies. During the cholera visitation of 1858 the air was
rich in ærobic and anærobic bacteria, while a blue mist which prevailed
throughout the epidemic yielded a far greater number than at any former
period (represented in Plate I., No. 13). This blue mist attracted the especial
attention of meteorologists. At a somewhat later period a more remarkable
fungoid disease, the fungus foot of India, mycetoma, came under my
observation, a detailed description of which I contributed to the medical
journals, and also, with further details, to the “Monthly Microscopical
Journal” of 1871. Interlacing mycelia, ending in hyphæ, in this destructive
form of parasitic disease were seen to pervade the whole of the tissues of
the foot, the bony structures being involved, and it was only possible to stay
the action of the parasite by amputation.
Page 427
So far, then, the study of parasitic organisms had at an early period shared
largely in my microscopical work, extending over several years, and with
the result that these micro-organisms were found to exhibit on occasions
great diversity of character, and that different members of the bacteria in
particular flourish under great diversity of action, and often under entirely
opposite conditions; that they feed upon wholly different materials, and
perform an immense variety of chemical work in the media in which they
live.
The study of the chemistry (chemotaxis) of bacteria has, however, greatly
enlarged our conception of the chemical value and power of the vegetable
cell, while it is obvious that no more appropriate or remunerative field of
study could engage the attention of the microscopist, as well as the chemist,
than that of bacterial life, and which is so well calculated to enlarge our
views of created organisms, whether belonging to the vegetable or animal
kingdom.
Pathogenic Fungi and Moulds.
It is scarcely necessary to go back to the history of the parasitic fungi to
which diseases of various kinds were early attributable. The rude
microscopes of two and a half centuries ago revealed the simple fact that all
decomposable substances swarmed with countless multitudes of organisms,
invisible to ordinary vision. Leuwenhoek, the father of microscopy, and
whose researches were generally known and accepted in 1675, tells of his
discovery of extremely minute organisms in rain-water, in vegetable
infusions, in saliva, and in scrapings from the teeth; further, he
differentiated these living organisms by their size and form, and illustrated
them by means of woodcuts; and there can be no doubt that his figures are
intended to represent leptothrix filaments, vibrios, and spirilla. In other of
his writings attempts are made to give an idea of the size of these
“animalcules”; he described them as a thousand times smaller than a grain
of sand. From his investigations a belief sprung up that malaria was
produced by “animalcules,” and that the plague which visited Toulon and
Marseilles in 1721 arose from a similar cause. Somewhat later on the
natural history of micro-organisms was more diligently studied, and with
largely in my microscopical work, extending over several years, and with
the result that these micro-organisms were found to exhibit on occasions
great diversity of character, and that different members of the bacteria in
particular flourish under great diversity of action, and often under entirely
opposite conditions; that they feed upon wholly different materials, and
perform an immense variety of chemical work in the media in which they
live.
The study of the chemistry (chemotaxis) of bacteria has, however, greatly
enlarged our conception of the chemical value and power of the vegetable
cell, while it is obvious that no more appropriate or remunerative field of
study could engage the attention of the microscopist, as well as the chemist,
than that of bacterial life, and which is so well calculated to enlarge our
views of created organisms, whether belonging to the vegetable or animal
kingdom.
Pathogenic Fungi and Moulds.
It is scarcely necessary to go back to the history of the parasitic fungi to
which diseases of various kinds were early attributable. The rude
microscopes of two and a half centuries ago revealed the simple fact that all
decomposable substances swarmed with countless multitudes of organisms,
invisible to ordinary vision. Leuwenhoek, the father of microscopy, and
whose researches were generally known and accepted in 1675, tells of his
discovery of extremely minute organisms in rain-water, in vegetable
infusions, in saliva, and in scrapings from the teeth; further, he
differentiated these living organisms by their size and form, and illustrated
them by means of woodcuts; and there can be no doubt that his figures are
intended to represent leptothrix filaments, vibrios, and spirilla. In other of
his writings attempts are made to give an idea of the size of these
“animalcules”; he described them as a thousand times smaller than a grain
of sand. From his investigations a belief sprung up that malaria was
produced by “animalcules,” and that the plague which visited Toulon and
Marseilles in 1721 arose from a similar cause. Somewhat later on the
natural history of micro-organisms was more diligently studied, and with
Page 428
increasing interest. Müller, in 1786, pointed out that they had been too
much given to occupy themselves in finding new organisms, he therefore
devoted himself to the study of their forms and biological characters, and it
was on such data he based a classification. Thus the scientific knowledge
gained of these minute bodies was considerably advanced, and the subject
now entered upon a new phase: the origin of micro-organisms. It further
resolved itself into two rival theories—spontaneous generation, and
development from pre-existing germs—the discussion over which lasted
more than a century. Indeed, it only ended in 1871, when the originator of
the Abiogenesis theory withdrew from the contest, and the more scientific
investigations of Pasteur (1861) found general acceptance. This
indefatigable worker had been investigating fermentation, and studying the
so-called diseases of wines and a contagious disease which was committing
ravages among silkworms. Pasteur in time was able to confirm the belief
that the “muscadine disease” of silkworms was due to the presence of
micro-organisms, discernible only by the microscope. The oval, shining
bodies in the moth, worm, and eggs had been previously observed and
described by Nägeli and others, but it was reserved for Pasteur to show that
when a silkworm whose body contained these organisms was pounded up in
a mortar with water, and painted over the leaves of the tree upon which
healthy worms were fed, all took the disease and died.
PLATE IX.
much given to occupy themselves in finding new organisms, he therefore
devoted himself to the study of their forms and biological characters, and it
was on such data he based a classification. Thus the scientific knowledge
gained of these minute bodies was considerably advanced, and the subject
now entered upon a new phase: the origin of micro-organisms. It further
resolved itself into two rival theories—spontaneous generation, and
development from pre-existing germs—the discussion over which lasted
more than a century. Indeed, it only ended in 1871, when the originator of
the Abiogenesis theory withdrew from the contest, and the more scientific
investigations of Pasteur (1861) found general acceptance. This
indefatigable worker had been investigating fermentation, and studying the
so-called diseases of wines and a contagious disease which was committing
ravages among silkworms. Pasteur in time was able to confirm the belief
that the “muscadine disease” of silkworms was due to the presence of
micro-organisms, discernible only by the microscope. The oval, shining
bodies in the moth, worm, and eggs had been previously observed and
described by Nägeli and others, but it was reserved for Pasteur to show that
when a silkworm whose body contained these organisms was pounded up in
a mortar with water, and painted over the leaves of the tree upon which
healthy worms were fed, all took the disease and died.
PLATE IX.
Page 429
AFTER DR CROOKSHANK J. T. Balcomb. del.
TYPICAL FORMS OF BACTERIA, SCHIZOMYCETES, OR FISSION-FUNGI.
As the contagious particles were transmitted to the eggs, the method
adopted for preventing the spread of the disease was as follows:—Each
female moth was kept separate from the others, and allowed to deposit her
eggs, and after death her body was crushed up in a mortar as before, and a
drop of the fluid examined under the microscope. When any trace of
muscadine was found present, the whole of the eggs and body were burnt.
In this way the disease was combated, and ultimately stamped out.
Pasteur also pointed out that one form or cause of disease must not be
confounded with another. For example, muscadine, a true fungus (Botrytis
bassiana), should not be confounded with another disease known to attack
silkworms, termed pebrin, this being caused by a bacterium, and, according
TYPICAL FORMS OF BACTERIA, SCHIZOMYCETES, OR FISSION-FUNGI.
As the contagious particles were transmitted to the eggs, the method
adopted for preventing the spread of the disease was as follows:—Each
female moth was kept separate from the others, and allowed to deposit her
eggs, and after death her body was crushed up in a mortar as before, and a
drop of the fluid examined under the microscope. When any trace of
muscadine was found present, the whole of the eggs and body were burnt.
In this way the disease was combated, and ultimately stamped out.
Pasteur also pointed out that one form or cause of disease must not be
confounded with another. For example, muscadine, a true fungus (Botrytis
bassiana), should not be confounded with another disease known to attack
silkworms, termed pebrin, this being caused by a bacterium, and, according
Page 430
to the more recent researches of Balbiani, by a Psorospermia. Botrytis is a
true mould, belonging to the Oomycetes, and allied to the potato fungus,
Peronospora. It is propagated by spores, which, falling on a silkworm,
germinate and penetrate its body. A mycelium is then developed, which
spreads throughout the body. Hyphæ appear through the skin, and bear
white chalky-looking spores; these become detached, and float in the air as
an impalpable dust-like smoke. Damp further develops the fungus.
Insects suffer much from the ravages of fungi. The house-fly sticking to the
window-pane is seen to be surrounded by the mycelia of Penicillium
racemosum (Sporendonema muscæ, or Saprolegnia feræ). In other cases
Cordiceps attacks certain caterpillars belonging to the genera Cossus and
Hepialus when they are buried in the sand and before their metamorphosis
into chrysalides; they are killed by the rapid development of hyphæ and
mycelium in their tissues.
Sphæria miletaris, a parasite of Bombyx pilyocarpa, the caterpillar of which
is found on pine-trees, is one of the few fungi which may be regarded as
beneficial to man, since it aids in the destruction of multitudes of these
caterpillars, which otherwise would devour the young shoots and pine
needles. Giard specialises other parasites of insects, which he terms
Entomophoreæ. Others, E. rimosa, attack grasshoppers and the diptera,
enveloping them in a dense coating of mycelium and spores, which speedily
kills the victim.
The study, then, of the life-history of germs, microbes, micro-organisms, or
bacteria (as they are indifferently termed), opened up a new science, that of
Bacteriology. By the more recent advances in this science we are enabled to
understand the very important part these minute organisms fill in the great
scheme of Nature, for almost exclusively by their agency the soil is
supplied with the requisite nutritive material for plant life. And, as already
pointed out, wherever organic matter is present—that is, the dead and
useless substances which are the refuse of life—such material is promptly
seized upon by micro-organisms, by means of which histolysis is rapidly
accomplished.
Bacteria require a power of from 600 to 1,000 diameters or more for the
determination of the species to which they belong. The number of species
true mould, belonging to the Oomycetes, and allied to the potato fungus,
Peronospora. It is propagated by spores, which, falling on a silkworm,
germinate and penetrate its body. A mycelium is then developed, which
spreads throughout the body. Hyphæ appear through the skin, and bear
white chalky-looking spores; these become detached, and float in the air as
an impalpable dust-like smoke. Damp further develops the fungus.
Insects suffer much from the ravages of fungi. The house-fly sticking to the
window-pane is seen to be surrounded by the mycelia of Penicillium
racemosum (Sporendonema muscæ, or Saprolegnia feræ). In other cases
Cordiceps attacks certain caterpillars belonging to the genera Cossus and
Hepialus when they are buried in the sand and before their metamorphosis
into chrysalides; they are killed by the rapid development of hyphæ and
mycelium in their tissues.
Sphæria miletaris, a parasite of Bombyx pilyocarpa, the caterpillar of which
is found on pine-trees, is one of the few fungi which may be regarded as
beneficial to man, since it aids in the destruction of multitudes of these
caterpillars, which otherwise would devour the young shoots and pine
needles. Giard specialises other parasites of insects, which he terms
Entomophoreæ. Others, E. rimosa, attack grasshoppers and the diptera,
enveloping them in a dense coating of mycelium and spores, which speedily
kills the victim.
The study, then, of the life-history of germs, microbes, micro-organisms, or
bacteria (as they are indifferently termed), opened up a new science, that of
Bacteriology. By the more recent advances in this science we are enabled to
understand the very important part these minute organisms fill in the great
scheme of Nature, for almost exclusively by their agency the soil is
supplied with the requisite nutritive material for plant life. And, as already
pointed out, wherever organic matter is present—that is, the dead and
useless substances which are the refuse of life—such material is promptly
seized upon by micro-organisms, by means of which histolysis is rapidly
accomplished.
Bacteria require a power of from 600 to 1,000 diameters or more for the
determination of the species to which they belong. The number of species
Page 431
has been so much increased of late that a bulky volume is found to be
insufficient for their enumeration. I am, however, by the courtesy of
Professor Crookshank, enabled to present my readers with the typical forms
of thirty-nine species of Bacteria, Schizomycetes, or fission-fungi, a
selection, it will be seen, chiefly taken from among pathogenic organisms—
those believed to originate disease. But many of the supposed Saprophytic
forms often described as originating disease are merely accidental
associates, that is, living in companionship for a time.
Size.—In ordinary terms of measurement, bacteria are on an average from
1⁄25000th to about 1⁄5000th of an inch long. These measurements do not convey
a definite impression to the mind. It is calculated that a thousand million of
them could be contained in a space of 1⁄25th of an inch. The best impression
of the size of the bacteria is, perhaps, obtained when it is stated that a 1⁄25-
inch immersion objective gives a magnification of nearly 2,200 diameters,
and that under this power the bacteria appear to be about the size of very
small print. The standard of measurement accepted by bacteriologists is the
micro-millimeter. One millimeter is equal to about 1⁄25000th an English inch.
The number of micrococci in a milligramme of a culture of Staphylococcus
pyogenes aurens has been estimated by Bujwid by counting at eight
thousand millions. Not only do various species differ in dimensions, but
considerable differences may be noted in a pure culture of the same species.
On the other hand, there are numerous species which so closely resemble
each other in size and shape that they cannot be differentiated by
microscopic examination alone, and we have to look to other
characteristics, as colour, growth in various culture media, pathogenic
power, chemical products, &c., in order to decide the question of identity.
Reproduction.—The reproduction of bacteria takes place for the most part
by fission and by spore formation. Fission is a process of splitting up or
division, whereby an organism divides into two or more parts, each of
which lives and divides in its turn. If certain organisms are watched under
the microscope, a coccus or bacillus will be seen to elongate and at the
same time become narrower, until its two halves become free, the two
individual organisms again dividing and subdividing in their turn. This kind
of reproduction is more readily seen in a higher class of unicellular
organisms, the desmids. If, however, the new organisms do not break away
insufficient for their enumeration. I am, however, by the courtesy of
Professor Crookshank, enabled to present my readers with the typical forms
of thirty-nine species of Bacteria, Schizomycetes, or fission-fungi, a
selection, it will be seen, chiefly taken from among pathogenic organisms—
those believed to originate disease. But many of the supposed Saprophytic
forms often described as originating disease are merely accidental
associates, that is, living in companionship for a time.
Size.—In ordinary terms of measurement, bacteria are on an average from
1⁄25000th to about 1⁄5000th of an inch long. These measurements do not convey
a definite impression to the mind. It is calculated that a thousand million of
them could be contained in a space of 1⁄25th of an inch. The best impression
of the size of the bacteria is, perhaps, obtained when it is stated that a 1⁄25-
inch immersion objective gives a magnification of nearly 2,200 diameters,
and that under this power the bacteria appear to be about the size of very
small print. The standard of measurement accepted by bacteriologists is the
micro-millimeter. One millimeter is equal to about 1⁄25000th an English inch.
The number of micrococci in a milligramme of a culture of Staphylococcus
pyogenes aurens has been estimated by Bujwid by counting at eight
thousand millions. Not only do various species differ in dimensions, but
considerable differences may be noted in a pure culture of the same species.
On the other hand, there are numerous species which so closely resemble
each other in size and shape that they cannot be differentiated by
microscopic examination alone, and we have to look to other
characteristics, as colour, growth in various culture media, pathogenic
power, chemical products, &c., in order to decide the question of identity.
Reproduction.—The reproduction of bacteria takes place for the most part
by fission and by spore formation. Fission is a process of splitting up or
division, whereby an organism divides into two or more parts, each of
which lives and divides in its turn. If certain organisms are watched under
the microscope, a coccus or bacillus will be seen to elongate and at the
same time become narrower, until its two halves become free, the two
individual organisms again dividing and subdividing in their turn. This kind
of reproduction is more readily seen in a higher class of unicellular
organisms, the desmids. If, however, the new organisms do not break away
Page 432
from each other, but remain connected in groups or clusters, they are termed
Staphylococci; if they remain connected in the form of a chain, or like a
string of beads, they are termed Streptococci. If the division takes place in
one plane, Diplococci are formed; if in two directions Tetracocci, or Tablet-
cocci, are formed. On account of this multiplication by fission, the generic
name of Schizomycetes, or fission-fungi, has been given to bacteria.
Spores.—A second method by which bacteria propagate is by spores. These
bodies are distinguished by their remarkable power of resistance to the
influence of temperature and the action of chemical reagents. Some of them
will resist their immersion in strong acid solutions for many hours; also
freezing and very high temperatures. Spore formation may take place in two
ways: firstly, by “endogenous spores” (internal spores); secondly, by
“arthrospores.”
Endogenous Spores.—When the formation of the spores takes place in the
mother-cell, the protoplasm is seen to contract, giving rise to one or more
highly refractive bodies, which are the spores. The enclosing membrane of
the organism then breaks away, leaving the spores free.
Arthrospores.—When the spore is not formed in the parent bacillus, but
when entire cells (owing to lack of favourable conditions of growth)
become converted into spores, the formation is known as “arthrogenous,”
the single individual being called an arthrospore. When the conditions are
again favourable, spores germinate, giving rise to new bacilli. The
germinating spore becomes elongated, and loses its bright appearance, the
outer membrane becomes ruptured, and the young bacillus is set free.
Certain conditions, such as the presence of oxygen in the case of the
anthrax bacillus, give rise to the formation of spores; while various kinds of
bacteria secure continuous existence by developing spores when there is
lack of proper food material.
With reference to the incredible rapidity with which the bacteria multiply
under conditions favourable to the growth and development, Cohn writes as
follows:—“Let us assume that a microbe divides into two within an hour,
then again into eight in the third hour, and so on. The number of microbes
thus produced in twenty-four hours would exceed sixteen and a half
millions; in two days they would increase to forty-seven trillions; and in a
Staphylococci; if they remain connected in the form of a chain, or like a
string of beads, they are termed Streptococci. If the division takes place in
one plane, Diplococci are formed; if in two directions Tetracocci, or Tablet-
cocci, are formed. On account of this multiplication by fission, the generic
name of Schizomycetes, or fission-fungi, has been given to bacteria.
Spores.—A second method by which bacteria propagate is by spores. These
bodies are distinguished by their remarkable power of resistance to the
influence of temperature and the action of chemical reagents. Some of them
will resist their immersion in strong acid solutions for many hours; also
freezing and very high temperatures. Spore formation may take place in two
ways: firstly, by “endogenous spores” (internal spores); secondly, by
“arthrospores.”
Endogenous Spores.—When the formation of the spores takes place in the
mother-cell, the protoplasm is seen to contract, giving rise to one or more
highly refractive bodies, which are the spores. The enclosing membrane of
the organism then breaks away, leaving the spores free.
Arthrospores.—When the spore is not formed in the parent bacillus, but
when entire cells (owing to lack of favourable conditions of growth)
become converted into spores, the formation is known as “arthrogenous,”
the single individual being called an arthrospore. When the conditions are
again favourable, spores germinate, giving rise to new bacilli. The
germinating spore becomes elongated, and loses its bright appearance, the
outer membrane becomes ruptured, and the young bacillus is set free.
Certain conditions, such as the presence of oxygen in the case of the
anthrax bacillus, give rise to the formation of spores; while various kinds of
bacteria secure continuous existence by developing spores when there is
lack of proper food material.
With reference to the incredible rapidity with which the bacteria multiply
under conditions favourable to the growth and development, Cohn writes as
follows:—“Let us assume that a microbe divides into two within an hour,
then again into eight in the third hour, and so on. The number of microbes
thus produced in twenty-four hours would exceed sixteen and a half
millions; in two days they would increase to forty-seven trillions; and in a
Page 433
week the number expressing them would be made up of fifty-one figures.
At the end of twenty-four hours the microbes descended from a single
individual would occupy 1⁄40th of a hollow cube, with edges 1⁄25th of an inch
long, but at the end of the following day would fill a space of twenty-seven
cubic inches, and in less than five days their volume would equal that of the
entire ocean.”
Again, Cohn estimated that a single bacillus weighs about
0·000,000,000,024,243,672 of a grain; forty thousand millions, 1 grain; 289
billions, 1 pound. After twenty-four hours the descendants from a single
bacillus would weigh 1⁄2666th of a grain; after two days, over a pound; after
three days, sixteen and a half million pounds, or 7,366 tons. It is quite
unneccessary to state that these figures are purely theoretical, and could
only be realised if there were no impediment to such rapid increase.
Fortunately, however, various checks, such as lack of food and
unfavourable physical conditions, intervene to prevent unmanageable
multiplication of these bodies.
These figures show, however, what a tremendous vital activity micro-
organisms do possess, and it will be seen later at what great speed they
increase in water, milk, broth, and other suitable media.
The following bacilli, among others, have numerous flagella distributed
over the whole of the organism: the bacillus of blue milk (Bacillus
cyanogenus)52; the bacillus of malignant œdema; the hay bacillus (Bacillus
subtilis); Proteus vulgaris, &c.
The following have only one or two flagella at the poles: the Bacillus
pyocyaneus, the Spirillum finkleri, the Spirillum choleræ Asiaticæ, &c.
The Spirillum undala, Spirillum rubrum, Spirillum concentricum, and
Sarcinæ, pocket-cocci, have several flagella.
Micrococcus agilis have also several flagella; these possibly arise from one
point. As I have already pointed out, the classification of the bacteria is one
of great difficulty, since new kinds are being constantly discovered, and at
At the end of twenty-four hours the microbes descended from a single
individual would occupy 1⁄40th of a hollow cube, with edges 1⁄25th of an inch
long, but at the end of the following day would fill a space of twenty-seven
cubic inches, and in less than five days their volume would equal that of the
entire ocean.”
Again, Cohn estimated that a single bacillus weighs about
0·000,000,000,024,243,672 of a grain; forty thousand millions, 1 grain; 289
billions, 1 pound. After twenty-four hours the descendants from a single
bacillus would weigh 1⁄2666th of a grain; after two days, over a pound; after
three days, sixteen and a half million pounds, or 7,366 tons. It is quite
unneccessary to state that these figures are purely theoretical, and could
only be realised if there were no impediment to such rapid increase.
Fortunately, however, various checks, such as lack of food and
unfavourable physical conditions, intervene to prevent unmanageable
multiplication of these bodies.
These figures show, however, what a tremendous vital activity micro-
organisms do possess, and it will be seen later at what great speed they
increase in water, milk, broth, and other suitable media.
The following bacilli, among others, have numerous flagella distributed
over the whole of the organism: the bacillus of blue milk (Bacillus
cyanogenus)52; the bacillus of malignant œdema; the hay bacillus (Bacillus
subtilis); Proteus vulgaris, &c.
The following have only one or two flagella at the poles: the Bacillus
pyocyaneus, the Spirillum finkleri, the Spirillum choleræ Asiaticæ, &c.
The Spirillum undala, Spirillum rubrum, Spirillum concentricum, and
Sarcinæ, pocket-cocci, have several flagella.
Micrococcus agilis have also several flagella; these possibly arise from one
point. As I have already pointed out, the classification of the bacteria is one
of great difficulty, since new kinds are being constantly discovered, and at
Page 434
present any attempt made in this direction can only be considered as quite
of a provisional nature.
The difficulties which stand in the way may be surmised from the fact that
Sarcinæ, pocket-cocci, were originally believed to be a single species,
described by me, under the name of Sarcina ventriculi, in the fourth edition
of my book, “as remarkable bodies invading the human and animal
stomach, and seriously interfering with its functions.”
The original woodcut of these curious
parasites is reproduced in Fig. 268, also in
Plate IX., No. 7, and which evidently
belong to a different species, numbering
thirty-nine altogether. Quite recently Mr. G.
H. Broadbent, M.R.C.S., Manchester, sent
Fig. 268.—Sarcinæ. me a supply of these interesting bodies
lately discovered by him in an infusion of
cow manure. On examining a drop with a power of 1500 diameters they
were discovered moving over the field of the microscope with a gyrating
motion by the aid of flagella projecting from each corner of the pocket.
After some days, having attained their full growth of four, eight or sixteen
in a pocket, they break up, and recommence the formative process. Sarcinæ
are certainly pathogenic in their nature. Cocci in groups, or asso-cocci, are
similarly associated. These several forms of spiro-bacteria are enclosed in a
transparent cell-wall, and are sometimes described as zooglæa.
Of bacteria the most characteristic groups are bacillus, bacterium, and a
species of clostridium, a bottle-shaped bacillus. It is, however, difficult to
draw a sharp line between so-called species.
Spiro-bacteria, or spirilla, possess short or long filaments, rigid or flexible,
and their movements are accordingly rotatory, or in the long axis of the
filaments. These bodies are again divided into comma bacilli, or vibrios—a
name invented by the older microscopists who first described them—some
species of which have a flagellate appendage, to which their movements are
due.
of a provisional nature.
The difficulties which stand in the way may be surmised from the fact that
Sarcinæ, pocket-cocci, were originally believed to be a single species,
described by me, under the name of Sarcina ventriculi, in the fourth edition
of my book, “as remarkable bodies invading the human and animal
stomach, and seriously interfering with its functions.”
The original woodcut of these curious
parasites is reproduced in Fig. 268, also in
Plate IX., No. 7, and which evidently
belong to a different species, numbering
thirty-nine altogether. Quite recently Mr. G.
H. Broadbent, M.R.C.S., Manchester, sent
Fig. 268.—Sarcinæ. me a supply of these interesting bodies
lately discovered by him in an infusion of
cow manure. On examining a drop with a power of 1500 diameters they
were discovered moving over the field of the microscope with a gyrating
motion by the aid of flagella projecting from each corner of the pocket.
After some days, having attained their full growth of four, eight or sixteen
in a pocket, they break up, and recommence the formative process. Sarcinæ
are certainly pathogenic in their nature. Cocci in groups, or asso-cocci, are
similarly associated. These several forms of spiro-bacteria are enclosed in a
transparent cell-wall, and are sometimes described as zooglæa.
Of bacteria the most characteristic groups are bacillus, bacterium, and a
species of clostridium, a bottle-shaped bacillus. It is, however, difficult to
draw a sharp line between so-called species.
Spiro-bacteria, or spirilla, possess short or long filaments, rigid or flexible,
and their movements are accordingly rotatory, or in the long axis of the
filaments. These bodies are again divided into comma bacilli, or vibrios—a
name invented by the older microscopists who first described them—some
species of which have a flagellate appendage, to which their movements are
due.
Page 435
Anthrax, Splenic Fever, has been long known to be prevalent among cattle
at certain seasons of the year, and is believed to originate from peculiar
conditions of climate and soil. This view of splenic fever on microscopical
examination proved an entire fallacy. Bollinger in 1872 discovered that the
blood of the affected animal was still virulent after death, owing to the
presence of the spores of the bacillus, and that the soil also became infected
and impregnated by the disease germs wherever the fever first broke out. In
1877 Dr. Koch made a more careful investigation into the source of the
disease, and was able to give a complete demonstration of the life-history of
the splenic fever bacillus, and to offer definite proofs of its pathogenic
properties. He pointed out that the rods grew in the blood and tissues by
lengthening and by cross division. Further, that they not only grew into long
leptothrix filaments but they produced enormous numbers of seeds or
spores. He watched the fusion of the rods to the formation of spores and the
sprouting of fresh rods. He furthermore inoculated a mouse, watched the
effect through several generations, and fully demonstrated that in the blood
and swollen spleen of the animal the same rods were always present.
Pasteur and Paul Bret pursued the same course of investigations, which
were always followed with precisely similar results. It was, however,
principally due to the researches of Koch that the doctrine of contagium
vivum was placed on a scientific basis.
Subsequently Koch formulated methods of cultivation, and dictated the
microscopical apparatus needful. Furthermore, he furnished postulates for
proving beyond doubt the existence of specific pathogenic micro-
organisms.
“The chain of evidence regarded by Dr. Koch as essential for proving the
existence of a pathogenic organism is as follows:—1. The micro-organism
must be found in the blood, lymph, or diseased tissue of man or animal
suffering from, or dead of the disease. 2. The micro-organism must be
isolated from the blood or tissue, and cultivated in suitable media—i.e.,
outside the animal body. These pure cultivations must be carried on through
successive generations of the organism. 3. Pure cultivation thus obtained
must, when introduced into the body of a healthy animal, produce the
disease in question. 4. In the inoculated animal the same micro-organism
must again be found. The chain of evidence will be still more complete if,
at certain seasons of the year, and is believed to originate from peculiar
conditions of climate and soil. This view of splenic fever on microscopical
examination proved an entire fallacy. Bollinger in 1872 discovered that the
blood of the affected animal was still virulent after death, owing to the
presence of the spores of the bacillus, and that the soil also became infected
and impregnated by the disease germs wherever the fever first broke out. In
1877 Dr. Koch made a more careful investigation into the source of the
disease, and was able to give a complete demonstration of the life-history of
the splenic fever bacillus, and to offer definite proofs of its pathogenic
properties. He pointed out that the rods grew in the blood and tissues by
lengthening and by cross division. Further, that they not only grew into long
leptothrix filaments but they produced enormous numbers of seeds or
spores. He watched the fusion of the rods to the formation of spores and the
sprouting of fresh rods. He furthermore inoculated a mouse, watched the
effect through several generations, and fully demonstrated that in the blood
and swollen spleen of the animal the same rods were always present.
Pasteur and Paul Bret pursued the same course of investigations, which
were always followed with precisely similar results. It was, however,
principally due to the researches of Koch that the doctrine of contagium
vivum was placed on a scientific basis.
Subsequently Koch formulated methods of cultivation, and dictated the
microscopical apparatus needful. Furthermore, he furnished postulates for
proving beyond doubt the existence of specific pathogenic micro-
organisms.
“The chain of evidence regarded by Dr. Koch as essential for proving the
existence of a pathogenic organism is as follows:—1. The micro-organism
must be found in the blood, lymph, or diseased tissue of man or animal
suffering from, or dead of the disease. 2. The micro-organism must be
isolated from the blood or tissue, and cultivated in suitable media—i.e.,
outside the animal body. These pure cultivations must be carried on through
successive generations of the organism. 3. Pure cultivation thus obtained
must, when introduced into the body of a healthy animal, produce the
disease in question. 4. In the inoculated animal the same micro-organism
must again be found. The chain of evidence will be still more complete if,
Page 436
from artificial culture, a chemical substance is obtained capable of
producing the disease quite independently of the living organism. It is not
enough to merely detect, or even artificially cultivate, a bacterium
associated with disease. An endeavour must be made to establish the exact
relationship of the bacteria to disease processes. In many instances disease
bacteria regarded as the actual contagia have been found, on a further
searching inquiry, to be entirely misleading. It is almost needless to remind
the enthusiast that the actual contagion of the disease must be fully
demonstrated.”
producing the disease quite independently of the living organism. It is not
enough to merely detect, or even artificially cultivate, a bacterium
associated with disease. An endeavour must be made to establish the exact
relationship of the bacteria to disease processes. In many instances disease
bacteria regarded as the actual contagia have been found, on a further
searching inquiry, to be entirely misleading. It is almost needless to remind
the enthusiast that the actual contagion of the disease must be fully
demonstrated.”
Page 437
Fig. 269.—Micro-Photograph of Typhoid Fever Bacteria. Magnified 1000 ×.
Taken by Leitz’s oil immersion 1⁄12-inch ocular No. 4, and sunlight exposure of
one minute.
Typhoid Bacillus (Fig. 269).—Rods 1 to 3µ in length, and ·5 to ·8µ in
breadth, and threads. Spore-formation has not been observed, but the
protoplasm may be broken up, producing appearances which may be
mistaken for spores. Actively motile, provided, some with a single and
others with very numerous flagella, which are from three to five times as
long as the bacillus itself. They stain readily in aqueous solutions of aniline
dyes; and grow rapidly at a temperature of about 60° Fahr. In plate
cultivations minute colonies are visible in thirty-six to forty-eight hours;
they are circular or oval, with an irregular margin. On agar they form a
whitish transparent layer, and they flourish in milk.
Taken by Leitz’s oil immersion 1⁄12-inch ocular No. 4, and sunlight exposure of
one minute.
Typhoid Bacillus (Fig. 269).—Rods 1 to 3µ in length, and ·5 to ·8µ in
breadth, and threads. Spore-formation has not been observed, but the
protoplasm may be broken up, producing appearances which may be
mistaken for spores. Actively motile, provided, some with a single and
others with very numerous flagella, which are from three to five times as
long as the bacillus itself. They stain readily in aqueous solutions of aniline
dyes; and grow rapidly at a temperature of about 60° Fahr. In plate
cultivations minute colonies are visible in thirty-six to forty-eight hours;
they are circular or oval, with an irregular margin. On agar they form a
whitish transparent layer, and they flourish in milk.
Page 438
Fig. 270.—Plague Bacillus, Bombay, 1897. Magnified 1200 ×.
The Plague (Pestis Bacillus).—The Bombay plague of 1897-98 will ever be
remembered as one of the most appalling visitations ever known. The
number of deaths will never be accurately determined, as the native
population, among whom the disease chiefly prevailed and became so fatal,
concealed their dead or carried them away by night. The outbreak from the
first proved to be most infectious, its incubation lasting from a few hours to
a week only. It prevailed in all the over-crowded native quarters of the city.
The rats and mice that infested the dwellings of the poor were found to be
equally susceptible with human beings, and these vermin also died by
hundreds. Those that survived left their holes and made off, in this way
helping to spread the infective virus. On examining the bodies of dead rats,
they were found to have swollen legs, the blood being filled by bacilli and
curious monads, with whip-like appendages. The bacillus of plague was
The Plague (Pestis Bacillus).—The Bombay plague of 1897-98 will ever be
remembered as one of the most appalling visitations ever known. The
number of deaths will never be accurately determined, as the native
population, among whom the disease chiefly prevailed and became so fatal,
concealed their dead or carried them away by night. The outbreak from the
first proved to be most infectious, its incubation lasting from a few hours to
a week only. It prevailed in all the over-crowded native quarters of the city.
The rats and mice that infested the dwellings of the poor were found to be
equally susceptible with human beings, and these vermin also died by
hundreds. Those that survived left their holes and made off, in this way
helping to spread the infective virus. On examining the bodies of dead rats,
they were found to have swollen legs, the blood being filled by bacilli and
curious monads, with whip-like appendages. The bacillus of plague was
Page 439
discovered by Kitasato in 1894; it is characterised by short rods with
rounded ends, and a clear space in the middle. The bacilli stain readily with
aniline dyes, and when cultivated on agar, white transparent colonies are
formed which present an iridescent appearance when examined by reflected
light. In addition to the bubonic swellings, the neighbouring lymphatic
glands were also swollen and blocked by bacilli.
Fig. 271.—Monads in Rat’s Blood, 1,200 ×. (Crookshank.)
a. Monad threading its way among the blood-corpuscles; b. Another with
pendulum movement attached to a corpuscle; c. Angular forms; d. Encysted forms;
e and f. The same seen edgeways.
My illustration (Fig. 270) is from a micro-photograph taken in 1897, when
the death rate stood very high. The general distribution of the bacilli,
together with phagocytes and the contents of swollen lymphatic glands,
magnified 1,200 ×, is from a preparation made in hospital. The monads
from the rat’s blood, 1200 ×, seen threading their way among the blood
corpuscles of a rat, and represented in Fig. 271, are somewhat larger than
those found in the Bombay rats, but the flagella in the latter were quite as
marked, while the encysted forms were wholly absent and the blood
corpuscles less crenated. The white bodies (Fig. 270) were in some
preparations, together with the lymphatic bodies, more numerous and more
swollen.
rounded ends, and a clear space in the middle. The bacilli stain readily with
aniline dyes, and when cultivated on agar, white transparent colonies are
formed which present an iridescent appearance when examined by reflected
light. In addition to the bubonic swellings, the neighbouring lymphatic
glands were also swollen and blocked by bacilli.
Fig. 271.—Monads in Rat’s Blood, 1,200 ×. (Crookshank.)
a. Monad threading its way among the blood-corpuscles; b. Another with
pendulum movement attached to a corpuscle; c. Angular forms; d. Encysted forms;
e and f. The same seen edgeways.
My illustration (Fig. 270) is from a micro-photograph taken in 1897, when
the death rate stood very high. The general distribution of the bacilli,
together with phagocytes and the contents of swollen lymphatic glands,
magnified 1,200 ×, is from a preparation made in hospital. The monads
from the rat’s blood, 1200 ×, seen threading their way among the blood
corpuscles of a rat, and represented in Fig. 271, are somewhat larger than
those found in the Bombay rats, but the flagella in the latter were quite as
marked, while the encysted forms were wholly absent and the blood
corpuscles less crenated. The white bodies (Fig. 270) were in some
preparations, together with the lymphatic bodies, more numerous and more
swollen.
Page 440
With regard to the conditions of life of the bacteria, they may be divided
broadly into two classes. When the organisms draw their nourishment from
some living body or “host,” they are known as “parasites.” These are further
termed “obligate” parasites if they exclusively live on their “host.” If the
bacteria draw their nourishment from dead organic matter, they are called
“saprophytes.” These are also divided into “obligate” and “facultative”
saprophytes. Thus it will be apparent that a parasite under certain
circumstances may readily become a saprophyte.
Some of the more important saprophytes are those organisms which play an
important and useful part in our every-day life, such as, for instance, in the
phenomena associated with fermentation, and putrefaction agents which
transform dead and decomposing organic matter into their simpler elements,
thus completing the great life cycle, and rendering the dead and effete
matter again ready for the vital processes.
Among other life manifestations of certain bacteria may be mentioned those
which have the property of generating colouring matter, though not
chlorophyll. The bacteria themselves are colourless and transparent, and the
pigment is merely formed as a product of their metabolism, especially
under the influence of light. Many of the bacteria give rise to various gases
and odours, particularly the anærobic organisms, which originate those foul
putrefactive gases (ammonia, sulphuretted hydrogen, &c.). The blood-rain,
Micrococcus prodigiosus, gives off an odour resembling trimethylamin.
Micro-organisms have the property of producing various changes in the
medium on which they are grown. In many cases albuminous bodies are
peptonized and gelatine is liquefied. Many bacteria have the faculty of
resolving organic bodies into their simplest elements; others, again, have
the property of converting ammonia into nitric and nitrous acid. Certain
microbes have the property of becoming phosphorescent in the dark. These
phosphorescent bacteria are often seen on decaying plants and wood;
sometimes in tropical climates the sea becomes luminous owing to the
presence of countless numbers of these organisms. Again, they are
frequently seen on the surface of dead fish, particularly mackerel, which
often become so bright as to strongly illuminate the cupboard in which they
lie.
broadly into two classes. When the organisms draw their nourishment from
some living body or “host,” they are known as “parasites.” These are further
termed “obligate” parasites if they exclusively live on their “host.” If the
bacteria draw their nourishment from dead organic matter, they are called
“saprophytes.” These are also divided into “obligate” and “facultative”
saprophytes. Thus it will be apparent that a parasite under certain
circumstances may readily become a saprophyte.
Some of the more important saprophytes are those organisms which play an
important and useful part in our every-day life, such as, for instance, in the
phenomena associated with fermentation, and putrefaction agents which
transform dead and decomposing organic matter into their simpler elements,
thus completing the great life cycle, and rendering the dead and effete
matter again ready for the vital processes.
Among other life manifestations of certain bacteria may be mentioned those
which have the property of generating colouring matter, though not
chlorophyll. The bacteria themselves are colourless and transparent, and the
pigment is merely formed as a product of their metabolism, especially
under the influence of light. Many of the bacteria give rise to various gases
and odours, particularly the anærobic organisms, which originate those foul
putrefactive gases (ammonia, sulphuretted hydrogen, &c.). The blood-rain,
Micrococcus prodigiosus, gives off an odour resembling trimethylamin.
Micro-organisms have the property of producing various changes in the
medium on which they are grown. In many cases albuminous bodies are
peptonized and gelatine is liquefied. Many bacteria have the faculty of
resolving organic bodies into their simplest elements; others, again, have
the property of converting ammonia into nitric and nitrous acid. Certain
microbes have the property of becoming phosphorescent in the dark. These
phosphorescent bacteria are often seen on decaying plants and wood;
sometimes in tropical climates the sea becomes luminous owing to the
presence of countless numbers of these organisms. Again, they are
frequently seen on the surface of dead fish, particularly mackerel, which
often become so bright as to strongly illuminate the cupboard in which they
lie.
Page 441
The particular class of fungi that produce disease in man and the higher
animals are generally known as “pathogenic.” These pathogenic organisms
may exert their pernicious power in several ways. They may be injurious on
account of their abstracting nourishment from the blood or tissues, or for
the purely mechanical reason of their stopping up the minute capillaries and
blood-vessels by their excessive multiplication. But the poisonous action of
most of the pathogenic bacteria is due to the chemical products secreted by
the organisms, and it is to the circulation and absorption within the body of
these poisons that the disturbances of the animal system, which characterise
disease, decay, and dissolution of every organism, must be traced.
Parasitic Diseases of Plants.
The subject of fungoid diseases and fungus epidemics are of worldwide
interest, if only because of the annual losses to agriculturists from parasitic
diseases of plants, amounting to millions of pounds sterling. The history of
wheat-rust, and that of oats and rye, each equally susceptible to the ravages
of the same Rufus, can be traced back to Genesis. A description of it was
given in 1805 by Sir Joseph Banks. He suggested that the germs entered the
stomata, and he warned farmers against the use of rusted litter, and made
important experiments on the sowing of rusted wheat-grains. A great
discussion on the barberry question followed, Fries particularly insisting on
the difference between Æcidium berberidis and Puccinia graminis. Tulasne
confirmed the statement made by Henslow that the uredo and puccinia
stages belong to the same fungus, and are not mixed species. De Bary’s
investigations in 1860-64 proved that the sporidia of some Uredinieæ (e.g.,
Coleosporium) will not infect the plant which bears the spores, and that the
æcidia of certain other forms are stages in the life-history of species of
Uromyces and Puccinia. Furthermore, De Bary in 1864 attacked the
question of wheat rust, and by means of numerous sowings of the
telentospores on barberry proved that they bring about the infection.
This led to the discovery of the phenomenon of Heterœcism (colonisation),
introducing a new idea, and clearing up many difficulties. In 1890 the rust
question entered on a new phase: it was taken up by men of science all over
the world, and active inquiries were set on foot. The result has been the
animals are generally known as “pathogenic.” These pathogenic organisms
may exert their pernicious power in several ways. They may be injurious on
account of their abstracting nourishment from the blood or tissues, or for
the purely mechanical reason of their stopping up the minute capillaries and
blood-vessels by their excessive multiplication. But the poisonous action of
most of the pathogenic bacteria is due to the chemical products secreted by
the organisms, and it is to the circulation and absorption within the body of
these poisons that the disturbances of the animal system, which characterise
disease, decay, and dissolution of every organism, must be traced.
Parasitic Diseases of Plants.
The subject of fungoid diseases and fungus epidemics are of worldwide
interest, if only because of the annual losses to agriculturists from parasitic
diseases of plants, amounting to millions of pounds sterling. The history of
wheat-rust, and that of oats and rye, each equally susceptible to the ravages
of the same Rufus, can be traced back to Genesis. A description of it was
given in 1805 by Sir Joseph Banks. He suggested that the germs entered the
stomata, and he warned farmers against the use of rusted litter, and made
important experiments on the sowing of rusted wheat-grains. A great
discussion on the barberry question followed, Fries particularly insisting on
the difference between Æcidium berberidis and Puccinia graminis. Tulasne
confirmed the statement made by Henslow that the uredo and puccinia
stages belong to the same fungus, and are not mixed species. De Bary’s
investigations in 1860-64 proved that the sporidia of some Uredinieæ (e.g.,
Coleosporium) will not infect the plant which bears the spores, and that the
æcidia of certain other forms are stages in the life-history of species of
Uromyces and Puccinia. Furthermore, De Bary in 1864 attacked the
question of wheat rust, and by means of numerous sowings of the
telentospores on barberry proved that they bring about the infection.
This led to the discovery of the phenomenon of Heterœcism (colonisation),
introducing a new idea, and clearing up many difficulties. In 1890 the rust
question entered on a new phase: it was taken up by men of science all over
the world, and active inquiries were set on foot. The result has been the
Page 442
confirmation of De Bary’s results, but with the further discovery that our
four common cereals are attacked by no less than ten different forms of rust
belonging to five separate species or “form species,” and with several
physiological varieties, capable of turning the table upon the barberry by
infecting it. Some of these are found to be strictly confined to one or other
of the four common cereals, infecting two or more of them, while others
can infect various kinds of our common wild grasses.
The fact is, that what has usually
gone by the name of Puccinia
graminis is an aggregate of several
species, and that varietal forms of
this exist so especially adapted to the
host, that, although no morphical
differences can be detected between
them, they cannot be transferred
from one cereal to another, pointing
to physiological variations of a kind
met with among bacteria and yeasts,
but hitherto unsuspected in these
higher parasitic fungi. It now appears
we must be prepared for similar
specialisation of varietal forms
among Ustilagineæ as well as among
Uredineæ.
Fig. 272.—Puccinia, displaying uredospores and
Moreover, it has been found that telentospores.
different sorts of wheat, oats, barley, a. Aregma speciosum; b. Xenodochus paradoxus;
and rye are susceptible to their c. P. Amorphæ; d. Triphœmium dubens; e.
particular rusts in different degrees, Younger spores; f. P. lateripes; magnified 450
diameters.
at the bottom of which, it is
suggested, there must be some
complex physiological causes. De Bary gave proof, in 1886, that Peziza
(Plate I., Nos. 1, 4, 5, 6) succeeds in becoming parasitic only after
saprophytic culture to a strong mycelium, and that its form is altered
thereby—probably by the excretion of a poison. Professor Marshall Ward
showed that similar results took place in the case of the lily disease.
four common cereals are attacked by no less than ten different forms of rust
belonging to five separate species or “form species,” and with several
physiological varieties, capable of turning the table upon the barberry by
infecting it. Some of these are found to be strictly confined to one or other
of the four common cereals, infecting two or more of them, while others
can infect various kinds of our common wild grasses.
The fact is, that what has usually
gone by the name of Puccinia
graminis is an aggregate of several
species, and that varietal forms of
this exist so especially adapted to the
host, that, although no morphical
differences can be detected between
them, they cannot be transferred
from one cereal to another, pointing
to physiological variations of a kind
met with among bacteria and yeasts,
but hitherto unsuspected in these
higher parasitic fungi. It now appears
we must be prepared for similar
specialisation of varietal forms
among Ustilagineæ as well as among
Uredineæ.
Fig. 272.—Puccinia, displaying uredospores and
Moreover, it has been found that telentospores.
different sorts of wheat, oats, barley, a. Aregma speciosum; b. Xenodochus paradoxus;
and rye are susceptible to their c. P. Amorphæ; d. Triphœmium dubens; e.
particular rusts in different degrees, Younger spores; f. P. lateripes; magnified 450
diameters.
at the bottom of which, it is
suggested, there must be some
complex physiological causes. De Bary gave proof, in 1886, that Peziza
(Plate I., Nos. 1, 4, 5, 6) succeeds in becoming parasitic only after
saprophytic culture to a strong mycelium, and that its form is altered
thereby—probably by the excretion of a poison. Professor Marshall Ward
showed that similar results took place in the case of the lily disease.
Page 443
Reinhardt, in 1892, showed that the apical growth of a peziza is disturbed
and interrupted if the culture solution is employed concentrated; and
Büsgen, in 1893, showed that Botrytis cinerea excretes poison at the tips of
the hyphæ, thus confirming Professor Ward’s results with the lily disease in
1888, and of later years, that a similar excretion occurs in rust-fungus. He
further found that the water contents of the infected plant exercises an
influence, as in the case of Botrytis attacking chrysanthemums and other
plants in the autumn, and that cold increases the germinating capacity of the
spores.
Pfeiffer, in his work on “Chemotaxis,” shows that bacteria will congregate
in the neighbourhood of an algal cell evolving oxygen. He also found that
many motile antherozoids, zoospores, bacteria, &c., when free to move in a
liquid, are attracted towards a point whence a given chemical substance is
diffusing. He was concerning himself less with the evolution of oxygen or
movements of bacteria than with a fundamental question of stimulation to
movement in general. He found the attractive power of different chemical
substances vary with the organism, and that various other bodies beside
oxygen attract bacteria—peptone, dextrose, potassium salts, &c.; that
swarm spores of the fungus Saprolegnia are powerfully attracted towards
the muscles of a fly’s leg placed in the water in which they are swimming
about; also, that in many cases where the hyphæ of fungi suddenly and
sharply bend out of their original course to enter the body of a plant or
animal, the cause of the bending lies in a powerful chemotropic action, due
to the attraction of some substance escaping from the body. Professor Ward
has seen zoospores of a Pythium suddenly dart out on to the cut surface of a
bean-stem, and there fix themselves.
This will be better understood by referring to the course pursued by these
bodies generally. When the spore of a parasitic fungus settles on a plant, it
frequently behaves as follows:—The spore germinates and forms a slender
tube of delicate consistency, blunt at the end, and containing colourless
protoplasm, as shown, highly magnified in Fig. 272, and in Figs. 273 and
274 much less magnified. De Bary long ago showed that such a tube—the
germinal-hypha—only grows for a short time along the surface of the
organ, and its tip soon bends down and enters the plant, either through one
of the stomata or by boring its way directly through the cell-walls. Professor
and interrupted if the culture solution is employed concentrated; and
Büsgen, in 1893, showed that Botrytis cinerea excretes poison at the tips of
the hyphæ, thus confirming Professor Ward’s results with the lily disease in
1888, and of later years, that a similar excretion occurs in rust-fungus. He
further found that the water contents of the infected plant exercises an
influence, as in the case of Botrytis attacking chrysanthemums and other
plants in the autumn, and that cold increases the germinating capacity of the
spores.
Pfeiffer, in his work on “Chemotaxis,” shows that bacteria will congregate
in the neighbourhood of an algal cell evolving oxygen. He also found that
many motile antherozoids, zoospores, bacteria, &c., when free to move in a
liquid, are attracted towards a point whence a given chemical substance is
diffusing. He was concerning himself less with the evolution of oxygen or
movements of bacteria than with a fundamental question of stimulation to
movement in general. He found the attractive power of different chemical
substances vary with the organism, and that various other bodies beside
oxygen attract bacteria—peptone, dextrose, potassium salts, &c.; that
swarm spores of the fungus Saprolegnia are powerfully attracted towards
the muscles of a fly’s leg placed in the water in which they are swimming
about; also, that in many cases where the hyphæ of fungi suddenly and
sharply bend out of their original course to enter the body of a plant or
animal, the cause of the bending lies in a powerful chemotropic action, due
to the attraction of some substance escaping from the body. Professor Ward
has seen zoospores of a Pythium suddenly dart out on to the cut surface of a
bean-stem, and there fix themselves.
This will be better understood by referring to the course pursued by these
bodies generally. When the spore of a parasitic fungus settles on a plant, it
frequently behaves as follows:—The spore germinates and forms a slender
tube of delicate consistency, blunt at the end, and containing colourless
protoplasm, as shown, highly magnified in Fig. 272, and in Figs. 273 and
274 much less magnified. De Bary long ago showed that such a tube—the
germinal-hypha—only grows for a short time along the surface of the
organ, and its tip soon bends down and enters the plant, either through one
of the stomata or by boring its way directly through the cell-walls. Professor
Page 444
Ward says these phenomena suggested to himself that the end of the tube is
attracted in some way, and by some force which brings its tip out of the
previous direction, and De Bary has suggested that this attraction is due to
some chemical substance excreted by the host plant. It is remarkable with
what ease the tube penetrates the cell-walls, and which Ward believes to be
due to the solvent action of an enzyme, capable of dissolving cellulose.
“Miyoshi carried these observations a step further when, in 1894, he
showed that if a leaf is injected with a substance such as ammonium-
chloride, dextrine, or cane-sugar (all substances capable of exerting
chemotropic attraction on fungus-hyphæ), and spores of a fungus which is
not parasitic are then sown on it, the hyphæ of the fungus penetrate the
stomata and behave exactly as if the fungus were a true parasite.
“So surprising a result lets in a flood of light on many known cases of
fungi, which are, as a rule, non-parasitic, becoming so, in fact, only when
the host plant is in an abnormal condition, e.g., the entry of species of
Botrytis into living tissues when the weather is cold and damp and the light
dull; the entry of Mucor into various fruits, tomatoes, apples, pears, &c.,
when the hyphæ meet with a slight crack or wound, through which the
juices are exposed. It is exceedingly probable that the rapid infection of
potato leaves in damp weather in July is traceable not merely to the
favouring effect of the moisture on the fungus, but that the state of super-
saturation of the cell-walls of the potato leaf—the tissues of which are now
unduly filled with water and dissolved sugars, &c., owing to the dull light
and diminished transpiration—is the primary factor which determines the
easy victory of the parasite, and, as Professor Ward suggested some time
ago, that the suppressed life of Ustilagineæ in the stems of grasses is due to
the want of particular carbo-hydrates in the vegetative tissues, but which are
present in the grain. A year later Miyoshi carried proof to demonstration,
and showed that a fungus-hypha is actually so attracted by substances on
the other side of a membrane, and that its tip pierces the latter; for the
hyphæ were made to grow through films of artificial cellulose, of collodion,
of cellulose impregnated with paraffin, of parchment paper, and even the
chitinous coat of an insect, simply by placing the intact films on gelatine
impregnated with the attracting substance, and laying the spores on the
opposite side of the membrane.
attracted in some way, and by some force which brings its tip out of the
previous direction, and De Bary has suggested that this attraction is due to
some chemical substance excreted by the host plant. It is remarkable with
what ease the tube penetrates the cell-walls, and which Ward believes to be
due to the solvent action of an enzyme, capable of dissolving cellulose.
“Miyoshi carried these observations a step further when, in 1894, he
showed that if a leaf is injected with a substance such as ammonium-
chloride, dextrine, or cane-sugar (all substances capable of exerting
chemotropic attraction on fungus-hyphæ), and spores of a fungus which is
not parasitic are then sown on it, the hyphæ of the fungus penetrate the
stomata and behave exactly as if the fungus were a true parasite.
“So surprising a result lets in a flood of light on many known cases of
fungi, which are, as a rule, non-parasitic, becoming so, in fact, only when
the host plant is in an abnormal condition, e.g., the entry of species of
Botrytis into living tissues when the weather is cold and damp and the light
dull; the entry of Mucor into various fruits, tomatoes, apples, pears, &c.,
when the hyphæ meet with a slight crack or wound, through which the
juices are exposed. It is exceedingly probable that the rapid infection of
potato leaves in damp weather in July is traceable not merely to the
favouring effect of the moisture on the fungus, but that the state of super-
saturation of the cell-walls of the potato leaf—the tissues of which are now
unduly filled with water and dissolved sugars, &c., owing to the dull light
and diminished transpiration—is the primary factor which determines the
easy victory of the parasite, and, as Professor Ward suggested some time
ago, that the suppressed life of Ustilagineæ in the stems of grasses is due to
the want of particular carbo-hydrates in the vegetative tissues, but which are
present in the grain. A year later Miyoshi carried proof to demonstration,
and showed that a fungus-hypha is actually so attracted by substances on
the other side of a membrane, and that its tip pierces the latter; for the
hyphæ were made to grow through films of artificial cellulose, of collodion,
of cellulose impregnated with paraffin, of parchment paper, and even the
chitinous coat of an insect, simply by placing the intact films on gelatine
impregnated with the attracting substance, and laying the spores on the
opposite side of the membrane.
Page 445
“Now this is obviously a point of the highest importance in the theory of
parasitism and parasitic diseases, because it suggests at once that in the
varying conditions of the cells, the contents of which are separated only by
membranous walls from the fungus-hyphæ, whose entrance means ruin and
destruction, there may be found circumstances which sometimes favour and
sometimes disfavour the entrance of the hyphæ; and it is, at least, a
remarkable fact that some of the substances which experiments prove to be
highly attractive to such hyphæ—e.g., sugars, the sap of plums, phosphates,
nitrates, &c.—are just the substances found in plants; and the discovery that
the action depends upon the nature of the substance as well as on the kind
of fungus, and is affected by its concentration, the temperature, and other
circumstances, only confirms us in this idea.”
Moreover, there is one other fact which it is important to notice, viz., that
there are substances which repel instead of attract the hyphæ. Is it not, then,
asks Professor Ward, natural to conclude that the differences in behaviour
of different parasites towards different host-plants, and towards the same
host-plant under different conditions, probably depend on the chemotropic
irritability of the hyphæ towards the substance formed in the cells on the
other side of the membranous cell-walls? And when, as often happens, the
effusion of substances, such as the cells contain, to the exterior is facilitated
by over-distension and super-saturation, or by actual wounds, we cannot be
surprised at the consequences when a fungus, hitherto unable to enter the
plant, suddenly does so. To this proposition my answer is emphatically in
the affirmative, since in my investigations into the “fungus-foot disease”
(“Mycetoma”), 1871, of India, the entry of the fungus was in almost every
case shown to be through an abrasion of the skin or a direct open wound;
the majority of the cases reported were among the agricultural classes.
When, then, as often happens, the effusion of substances, such as the cells
contain, to the exterior is facilitated by over-distension and super-saturation,
or by actual wounds, we cannot be surprised at the consequences when a
fungus, hitherto unable to enter the plant, suddenly does so. Nevertheless, it
must be admitted that the knowledge gained of parasites does not
satisfactorily account for epidemic visitations over large areas.
Habitat of Fungi and Moulds.
parasitism and parasitic diseases, because it suggests at once that in the
varying conditions of the cells, the contents of which are separated only by
membranous walls from the fungus-hyphæ, whose entrance means ruin and
destruction, there may be found circumstances which sometimes favour and
sometimes disfavour the entrance of the hyphæ; and it is, at least, a
remarkable fact that some of the substances which experiments prove to be
highly attractive to such hyphæ—e.g., sugars, the sap of plums, phosphates,
nitrates, &c.—are just the substances found in plants; and the discovery that
the action depends upon the nature of the substance as well as on the kind
of fungus, and is affected by its concentration, the temperature, and other
circumstances, only confirms us in this idea.”
Moreover, there is one other fact which it is important to notice, viz., that
there are substances which repel instead of attract the hyphæ. Is it not, then,
asks Professor Ward, natural to conclude that the differences in behaviour
of different parasites towards different host-plants, and towards the same
host-plant under different conditions, probably depend on the chemotropic
irritability of the hyphæ towards the substance formed in the cells on the
other side of the membranous cell-walls? And when, as often happens, the
effusion of substances, such as the cells contain, to the exterior is facilitated
by over-distension and super-saturation, or by actual wounds, we cannot be
surprised at the consequences when a fungus, hitherto unable to enter the
plant, suddenly does so. To this proposition my answer is emphatically in
the affirmative, since in my investigations into the “fungus-foot disease”
(“Mycetoma”), 1871, of India, the entry of the fungus was in almost every
case shown to be through an abrasion of the skin or a direct open wound;
the majority of the cases reported were among the agricultural classes.
When, then, as often happens, the effusion of substances, such as the cells
contain, to the exterior is facilitated by over-distension and super-saturation,
or by actual wounds, we cannot be surprised at the consequences when a
fungus, hitherto unable to enter the plant, suddenly does so. Nevertheless, it
must be admitted that the knowledge gained of parasites does not
satisfactorily account for epidemic visitations over large areas.
Habitat of Fungi and Moulds.
Page 446
Fig. 273.—Fungi and Moulds.
Description of Figures.—a. Fungi Spores, taken in a sick chamber; b. Aspergillus
glaucus; c. Yeast, recent state; d. Exhausted yeast, budding; e. Penicillium spores
more highly magnified; g. Aerobic spores and mould mycelium; h. Aspergillus
spore, grown on melon.
Habitat, Specialised Forms of Parasites.
Habitat.—The habitat of vegetable parasitic fungi is extremely variable.
Fungi are found everywhere, living and flourishing on all the families of the
vegetable and animal kingdoms. They attack our houses, foods, clothes,
utensils of every kind, wall papers and books, the paste of which, to my
astonishment, affords a sufficient supply of nourishment. Members of the
parasitic tribe of bacteria, by a combined effort of countless myriads, have
given rise to a sense of supernatural agency. Bacillus prodigiosus, described
also as Palmella mirifica and Zoogalactina imetropia, from its attacking
milk and other alimentary substances, the spores of which are often of a
deep red colour, have been found to cover whole tracts of country in a
single night with what is called a “gory dew,” changing in daylight to a
deep green colour. This was at one time regarded with superstitious awe as
a miracle, as it has been known to attack bread and even the sacred wafer,
and which in mediæval ages was described as the “bleeding-host.” This
parasitic plant belongs to anærobic bacteria, and is only developed in the
dark. The nitrogen required for nutrition must be derived from the air. An
algal form gives rise to the red scum seen in ponds and reservoirs in the
Description of Figures.—a. Fungi Spores, taken in a sick chamber; b. Aspergillus
glaucus; c. Yeast, recent state; d. Exhausted yeast, budding; e. Penicillium spores
more highly magnified; g. Aerobic spores and mould mycelium; h. Aspergillus
spore, grown on melon.
Habitat, Specialised Forms of Parasites.
Habitat.—The habitat of vegetable parasitic fungi is extremely variable.
Fungi are found everywhere, living and flourishing on all the families of the
vegetable and animal kingdoms. They attack our houses, foods, clothes,
utensils of every kind, wall papers and books, the paste of which, to my
astonishment, affords a sufficient supply of nourishment. Members of the
parasitic tribe of bacteria, by a combined effort of countless myriads, have
given rise to a sense of supernatural agency. Bacillus prodigiosus, described
also as Palmella mirifica and Zoogalactina imetropia, from its attacking
milk and other alimentary substances, the spores of which are often of a
deep red colour, have been found to cover whole tracts of country in a
single night with what is called a “gory dew,” changing in daylight to a
deep green colour. This was at one time regarded with superstitious awe as
a miracle, as it has been known to attack bread and even the sacred wafer,
and which in mediæval ages was described as the “bleeding-host.” This
parasitic plant belongs to anærobic bacteria, and is only developed in the
dark. The nitrogen required for nutrition must be derived from the air. An
algal form gives rise to the red scum seen in ponds and reservoirs in the
Page 447
autumn. The discharge from wounds is coloured blue by Bacterium
pyocyanine. There are many other forms, some of which have an orange
colour, and the genus is recognised as “chromogenic microbes.”
A cryptogam belonging to anærobic
bacteria, described as Protococcus
invalis, on being set aside in a bottle,
and a little rain water added, was
seen to set up spontaneous
fermentation, and in a very short
time exhibited remarkable activity.
The colour of the infusion changed,
it assumed a delicate pink hue in
direct light, which deepened to a red
in reflected light. The fluid contents
Fig. 274.—Fungi and Moulds.
were now observed to be dichoric,
Description of Figures.—d. Puccinia graminis on and the spectroscopic appearance
wheat; c. Polycystis spore of rye-smut; f. Alder subsequently presented was one of
fungus spores, Microspheria penicellula; g.
Dactylium roseum, rose-coloured mould; h. much interest. The spectrum was a
Verticillium distans, whorled mould found on well-marked one, and might be taken
herbaceous plants; i. Botrytis, vine and lily to determine the presence of a
fungus; j, j′. Peronospora infestans, potato
fungus; k. P. gangliformis, mould of herbaceous nitrogenous element or of glucose.
plants; l. Various Penicillium and other spores
taken in a bean-field. Among all the various plants known
to suffer from the attacks of
parasites, the vine has been the greatest sufferer. The oïdium, or Erysiphe
Tuckeri, so called from the name of the discoverer by whom it was first
described, has been longest known to the vine grower. This really belongs
to the group Ascomycetes, and appears to have been brought from America
in 1845, whence it was passed on to France, where it soon threatened to
entirely destroy the vineyards. This was followed by another parasite,
belonging in this instance to the animal kingdom, Phylloxera vastatrix. This
oïdium appears on the grape in the form of greyish filaments, terminating in
an enlarged head, which contains an agglomeration of spores, not free or in
a chaplet, as in Aspergillus (Fig. 273). These spores when ripe burst from
the capsule as fine dust, and are diffused by the air in all directions, thus
spreading the disease far and away. Another of the parasitic moulds,
pyocyanine. There are many other forms, some of which have an orange
colour, and the genus is recognised as “chromogenic microbes.”
A cryptogam belonging to anærobic
bacteria, described as Protococcus
invalis, on being set aside in a bottle,
and a little rain water added, was
seen to set up spontaneous
fermentation, and in a very short
time exhibited remarkable activity.
The colour of the infusion changed,
it assumed a delicate pink hue in
direct light, which deepened to a red
in reflected light. The fluid contents
Fig. 274.—Fungi and Moulds.
were now observed to be dichoric,
Description of Figures.—d. Puccinia graminis on and the spectroscopic appearance
wheat; c. Polycystis spore of rye-smut; f. Alder subsequently presented was one of
fungus spores, Microspheria penicellula; g.
Dactylium roseum, rose-coloured mould; h. much interest. The spectrum was a
Verticillium distans, whorled mould found on well-marked one, and might be taken
herbaceous plants; i. Botrytis, vine and lily to determine the presence of a
fungus; j, j′. Peronospora infestans, potato
fungus; k. P. gangliformis, mould of herbaceous nitrogenous element or of glucose.
plants; l. Various Penicillium and other spores
taken in a bean-field. Among all the various plants known
to suffer from the attacks of
parasites, the vine has been the greatest sufferer. The oïdium, or Erysiphe
Tuckeri, so called from the name of the discoverer by whom it was first
described, has been longest known to the vine grower. This really belongs
to the group Ascomycetes, and appears to have been brought from America
in 1845, whence it was passed on to France, where it soon threatened to
entirely destroy the vineyards. This was followed by another parasite,
belonging in this instance to the animal kingdom, Phylloxera vastatrix. This
oïdium appears on the grape in the form of greyish filaments, terminating in
an enlarged head, which contains an agglomeration of spores, not free or in
a chaplet, as in Aspergillus (Fig. 273). These spores when ripe burst from
the capsule as fine dust, and are diffused by the air in all directions, thus
spreading the disease far and away. Another of the parasitic moulds,
Page 448
Peronospora viticola, is a kind of mildew, differing from oïdium. The
hyphæ penetrate more deeply than that of oïdium. On the upper surface of
the leaf brown patches appear; these branch out and ramify as seen in the
potato-fungus, P. infestans (Fig. 274). The parasite destroys the tissue of the
leaf, and it withers and dies. There are other well-known parasites, the
black-rot, Phomauvicola, belonging to the Ascomycetes. This appears in
early shoots in the form of round black spots, and gradually spreads over
leaves and young fruit. This same rot, one year, devastated the American
vineyards.
Cereals, wheats and grasses, suffer
from other well-known forms of
microscopic fungi termed rusts and
smuts, which cover the blades or
infect the full ear of the fruit. The
name given indicates their colour,
and these belong, for the most part,
to the genus Uredo and the family of
the Basidiomycetes. They have no
endogenous spores but as many as
four forms of exogenous. This is also
the case with wheat and barley, Fig. 275.—Fungi, Moulds.
whereby they are distinguished as
Uredo or Puccinia graminis (see a. Clustered Spores, Gonatobotrys simplex; b.
Spore of Puccinia coronata, the mildew of
Figs. 273 and 274, and Plate I., Nos. grapes; c. Barley smut; d. Puccinia althæa; e.
19 and 22, Æcidium berberidis). For Penicillium glaucum; m. Ixodes farinæ, found in
damaged flour together with smut.
a long time it was believed that
Uredo linearis and Puccinia
graminis were so many distinct species, but it is now known that there are
only three successive phases of the developmental stages of a single species
—that, as a matter of fact, puccinia presents the phenomenon of alternation
of generations, that is, that the complete development of the fungus is only
effected by its transference from one plant to another. Other uredines,
Ustilago and Tilletia smuts, are more apt to affect the ears of wheat, rye,
and other grasses than puccinia. Bread made from wheat affected by smut
has an acrid and bitter taste, while that made from rye flour often produces
a serious form of disease. The propagation of either, then, should be stopped
hyphæ penetrate more deeply than that of oïdium. On the upper surface of
the leaf brown patches appear; these branch out and ramify as seen in the
potato-fungus, P. infestans (Fig. 274). The parasite destroys the tissue of the
leaf, and it withers and dies. There are other well-known parasites, the
black-rot, Phomauvicola, belonging to the Ascomycetes. This appears in
early shoots in the form of round black spots, and gradually spreads over
leaves and young fruit. This same rot, one year, devastated the American
vineyards.
Cereals, wheats and grasses, suffer
from other well-known forms of
microscopic fungi termed rusts and
smuts, which cover the blades or
infect the full ear of the fruit. The
name given indicates their colour,
and these belong, for the most part,
to the genus Uredo and the family of
the Basidiomycetes. They have no
endogenous spores but as many as
four forms of exogenous. This is also
the case with wheat and barley, Fig. 275.—Fungi, Moulds.
whereby they are distinguished as
Uredo or Puccinia graminis (see a. Clustered Spores, Gonatobotrys simplex; b.
Spore of Puccinia coronata, the mildew of
Figs. 273 and 274, and Plate I., Nos. grapes; c. Barley smut; d. Puccinia althæa; e.
19 and 22, Æcidium berberidis). For Penicillium glaucum; m. Ixodes farinæ, found in
damaged flour together with smut.
a long time it was believed that
Uredo linearis and Puccinia
graminis were so many distinct species, but it is now known that there are
only three successive phases of the developmental stages of a single species
—that, as a matter of fact, puccinia presents the phenomenon of alternation
of generations, that is, that the complete development of the fungus is only
effected by its transference from one plant to another. Other uredines,
Ustilago and Tilletia smuts, are more apt to affect the ears of wheat, rye,
and other grasses than puccinia. Bread made from wheat affected by smut
has an acrid and bitter taste, while that made from rye flour often produces
a serious form of disease. The propagation of either, then, should be stopped
Page 449
as quickly as possible by destroying all barberry bushes growing near or
within the vicinity of corn fields, and by other means. The ergot of rye is
due to distinct species of fungi having endogenous spores enclosed in a sac
or ascus, hence the name of the family, Ascomycetes or Tuberaceæ, which
are reproduced by the spores contained in these asci. Truffles belong to this
family. But other members of the same family have several forms of spores,
and these again present us with the phenomenon of alternation of
generations.
Ergot of rye is used in medicine, but
if not used with care it will produce a
dangerous disease. This parasitic
fungi consists of minute microscopic
masses of spores, which cover the
young flower of the rye with a white
flocculent mass, formerly termed
sphacelium. The mycelium formed
spreads over the ear of corn in thick
felt-like masses, termed sclerotis.
The sphacelium changes its form in
Fig. 276.—Fungi, Moulds. the following spring. Other changes
are brought about, and it seems to
p. Spores of Tilletia caries; q. Spores of Tilletia
caries, when germinating, produce a fœtid olive- pass through a cycle of alternations
coloured spore in cereal grains; r. Telentospores of generations.
of Puccinia graminis; s. Crystopus candidus,
spores growing in chains; t. Petronospora
infestans, mildew of turnips, &c.; u. A transverse
Bread made from rye so infested is
section of ergot of rye, showing spores in masses; known to produce grave
v. Claviceps purpuræ, associated with ergoted consequences, soon to become fatal
rye.
if not detected in time. The disease is
termed ergotism, and gangrene of the
extremities takes place among people of the north of France and Russia,
who consume bread made from rye flour. Ergot of maize will also cause
similar diseases. Fowls and other animals fed upon this cereal become in a
short time poisoned, and the cause of death is not rightly suspected. There is
another fungus belonging to the same group of Ascomycetes, known as
Eurotium repens, which appears upon leather when left in a damp place,
within the vicinity of corn fields, and by other means. The ergot of rye is
due to distinct species of fungi having endogenous spores enclosed in a sac
or ascus, hence the name of the family, Ascomycetes or Tuberaceæ, which
are reproduced by the spores contained in these asci. Truffles belong to this
family. But other members of the same family have several forms of spores,
and these again present us with the phenomenon of alternation of
generations.
Ergot of rye is used in medicine, but
if not used with care it will produce a
dangerous disease. This parasitic
fungi consists of minute microscopic
masses of spores, which cover the
young flower of the rye with a white
flocculent mass, formerly termed
sphacelium. The mycelium formed
spreads over the ear of corn in thick
felt-like masses, termed sclerotis.
The sphacelium changes its form in
Fig. 276.—Fungi, Moulds. the following spring. Other changes
are brought about, and it seems to
p. Spores of Tilletia caries; q. Spores of Tilletia
caries, when germinating, produce a fœtid olive- pass through a cycle of alternations
coloured spore in cereal grains; r. Telentospores of generations.
of Puccinia graminis; s. Crystopus candidus,
spores growing in chains; t. Petronospora
infestans, mildew of turnips, &c.; u. A transverse
Bread made from rye so infested is
section of ergot of rye, showing spores in masses; known to produce grave
v. Claviceps purpuræ, associated with ergoted consequences, soon to become fatal
rye.
if not detected in time. The disease is
termed ergotism, and gangrene of the
extremities takes place among people of the north of France and Russia,
who consume bread made from rye flour. Ergot of maize will also cause
similar diseases. Fowls and other animals fed upon this cereal become in a
short time poisoned, and the cause of death is not rightly suspected. There is
another fungus belonging to the same group of Ascomycetes, known as
Eurotium repens, which appears upon leather when left in a damp place,
Page 450
and also upon vegetable or animal substances if badly preserved, and
gradually destroys it. This mould is of a darkish green colour.
The minute spores display themselves as rows of beads when fully ripe on
the erect mycelium. Aspergillus glaucus represents the white exogenous
spores of the sphacelium of the ergot of rye; and those subsequently
produced in the yellow balls correspond with the asci developed in
sclerotis, the endogenous species. Many of the parasitic species belonging
to the genera Erysiphe, Sphæria, Sordaria, Penicillium, &c., have a similar
mode of propagation, and affect a large number of plants.
Parasitic Fungi of Men and Animals.
In the microscopical examinations especially given to the elucidation of
parasitic diseases of the skin, previously referred to, I discovered more
varieties of spores and filaments of certain cryptogamic plants associated
with a larger number of specific forms of fungi than any previous observer.
I did not, however, feel justified in concluding, with Küchenmeister,
Schœnlein, and Robin, that these fungoid growths were the primary cause
of the diseases referred to. Indeed, the foremost dermatologists of the period
utterly refused to entertain the specific germ theory of the German
investigators. Nevertheless, I contended, “the universality of their
distribution is in itself a fact of very considerable importance, and one
pointing to the belief that they are scavengers ever ready to fasten on
decaying matter, and, on finding a suitable soil, spread out their invisible
filaments in every direction in so persistent a manner as to arrest growth
and overwhelm the plant in destruction.”53
Special forms of fungi are given in Plate I., Nos. 10-14, and those of the
ascomycetes in Nos. 17-21.
Oïdium albicans affects both animals and plants. It often attacks the mucous
membrane of the mouths of young children. The spores become elongated
and converted into hyphæ, and ramify about in all directions, producing a
troublesome form of disease. This parasitic fungus is better known under
another name, Saccharomyces mycoderma. Oïdium resemble algæ in their
gradually destroys it. This mould is of a darkish green colour.
The minute spores display themselves as rows of beads when fully ripe on
the erect mycelium. Aspergillus glaucus represents the white exogenous
spores of the sphacelium of the ergot of rye; and those subsequently
produced in the yellow balls correspond with the asci developed in
sclerotis, the endogenous species. Many of the parasitic species belonging
to the genera Erysiphe, Sphæria, Sordaria, Penicillium, &c., have a similar
mode of propagation, and affect a large number of plants.
Parasitic Fungi of Men and Animals.
In the microscopical examinations especially given to the elucidation of
parasitic diseases of the skin, previously referred to, I discovered more
varieties of spores and filaments of certain cryptogamic plants associated
with a larger number of specific forms of fungi than any previous observer.
I did not, however, feel justified in concluding, with Küchenmeister,
Schœnlein, and Robin, that these fungoid growths were the primary cause
of the diseases referred to. Indeed, the foremost dermatologists of the period
utterly refused to entertain the specific germ theory of the German
investigators. Nevertheless, I contended, “the universality of their
distribution is in itself a fact of very considerable importance, and one
pointing to the belief that they are scavengers ever ready to fasten on
decaying matter, and, on finding a suitable soil, spread out their invisible
filaments in every direction in so persistent a manner as to arrest growth
and overwhelm the plant in destruction.”53
Special forms of fungi are given in Plate I., Nos. 10-14, and those of the
ascomycetes in Nos. 17-21.
Oïdium albicans affects both animals and plants. It often attacks the mucous
membrane of the mouths of young children. The spores become elongated
and converted into hyphæ, and ramify about in all directions, producing a
troublesome form of disease. This parasitic fungus is better known under
another name, Saccharomyces mycoderma. Oïdium resemble algæ in their
Page 451
mode of life, as they are mostly
found in a liquid media. The
structure of all ferments is very
simple: each plant is composed of a
single cell, either of a spherical,
elliptical, or cylindrical form,
varying in size, and filled with
protoplasmic and nucleated matter.
This grows, and is seen to bud out
and divide into two or more parts, all
resembling the mother cell.
Fig. 277 represents the healthy cells
of yeast, Saccharomyces cerevisiæ,
freshly taken from a brewer’s vat,
Fig. 277.—Healthy fresh Yeast, from a large
Brewery, in an active stage of formation, × and in an active stage of growth. The
400. mode of multiplication continues as
long as the plant remains in a liquid
favourable to its nutrition.
The changes from one stage to another are rapid, as will be noticed on
reference to the consecutive formative processes the cells are known to pass
through, Fig. 278 (1859).
If the development of the plant is arrested by want of a saccharine or
nitrogenous substance, and the liquid dries up, the protoplasm contained in
the cell contracts, and the spores, or endogenous reproductive organs, of the
plant will remain in a state of rest, become perfectly dry, and yet retain life.
They are not easily killed, even when subjected to a very high or low
temperature, they do not lose the power of germination when favourable
conditions present themselves, and at once take on a new birth.
There are, however, many other ferments besides that of beer-yeasts, such
as alcoholic and wine ferments, the commonest of which, according to
Pasteur, is Saccharomyces ellipsoideus.
found in a liquid media. The
structure of all ferments is very
simple: each plant is composed of a
single cell, either of a spherical,
elliptical, or cylindrical form,
varying in size, and filled with
protoplasmic and nucleated matter.
This grows, and is seen to bud out
and divide into two or more parts, all
resembling the mother cell.
Fig. 277 represents the healthy cells
of yeast, Saccharomyces cerevisiæ,
freshly taken from a brewer’s vat,
Fig. 277.—Healthy fresh Yeast, from a large
Brewery, in an active stage of formation, × and in an active stage of growth. The
400. mode of multiplication continues as
long as the plant remains in a liquid
favourable to its nutrition.
The changes from one stage to another are rapid, as will be noticed on
reference to the consecutive formative processes the cells are known to pass
through, Fig. 278 (1859).
If the development of the plant is arrested by want of a saccharine or
nitrogenous substance, and the liquid dries up, the protoplasm contained in
the cell contracts, and the spores, or endogenous reproductive organs, of the
plant will remain in a state of rest, become perfectly dry, and yet retain life.
They are not easily killed, even when subjected to a very high or low
temperature, they do not lose the power of germination when favourable
conditions present themselves, and at once take on a new birth.
There are, however, many other ferments besides that of beer-yeasts, such
as alcoholic and wine ferments, the commonest of which, according to
Pasteur, is Saccharomyces ellipsoideus.
Page 452
Fig. 278.—Development of Yeast Cells.
1. When first taken; 2. One hour after introducing a few cells into sweet-wort; 3.
Three hours after; 4. Eight hours; 5. Forty-eight hours, when the cells become
elongated.
But yeast-fungi and mould-fungi, like bacteria or fission-fungi, are micro-
organisms, belonging to two specific orders, the Saccharomycetes and the
Hyphomycetes, which are intimately related to each other, but quite distinct
from bacteria. Their germs occur widely distributed in air, soil, and water.
Many species are of hygienic, while others are of pathological interest and
importance in being either accidentally associated with, or the cause of,
disease processes, while others are fermentations of very essential service in
various industrial processes. The making of beers, wines, and spirits, as we
understand them, constitutes but a small part of the province of
fermentation. The life activities of ferments open out a study of vast
importance to mankind, and while they have only been regarded in their
worst aspect—that of a bane—they are, nevertheless, a boon to mankind.
The first clear view we obtained of this was that of Reess, who in 1870
showed there were several species or forms of the yeast-fungus. Hansen
followed up this discovery in 1883, and, taking advantage of the strict
methods of culture introduced by bacteriologists, found that by cultivating
1. When first taken; 2. One hour after introducing a few cells into sweet-wort; 3.
Three hours after; 4. Eight hours; 5. Forty-eight hours, when the cells become
elongated.
But yeast-fungi and mould-fungi, like bacteria or fission-fungi, are micro-
organisms, belonging to two specific orders, the Saccharomycetes and the
Hyphomycetes, which are intimately related to each other, but quite distinct
from bacteria. Their germs occur widely distributed in air, soil, and water.
Many species are of hygienic, while others are of pathological interest and
importance in being either accidentally associated with, or the cause of,
disease processes, while others are fermentations of very essential service in
various industrial processes. The making of beers, wines, and spirits, as we
understand them, constitutes but a small part of the province of
fermentation. The life activities of ferments open out a study of vast
importance to mankind, and while they have only been regarded in their
worst aspect—that of a bane—they are, nevertheless, a boon to mankind.
The first clear view we obtained of this was that of Reess, who in 1870
showed there were several species or forms of the yeast-fungus. Hansen
followed up this discovery in 1883, and, taking advantage of the strict
methods of culture introduced by bacteriologists, found that by cultivating
Page 453
yeast on a solid media from a single spore it was quite possible to obtain
constant types of pure yeasts, each possessing its own peculiar properties.
One consequence of Hansen’s labours was that it now became possible for
every brewer to work with a yeast of uniform type instead of with
haphazard mixtures, in which serious disease forms might predominate and
injure the beer. Among other things made clear was that a true yeast may
have a mycelial stage of development. Furthermore, there is the influence
exercised by the nucleus of the yeast cell. Many other points of interest
arose out of these investigations; one was, that many higher fungi can
assume a yeast-like stage of development if submerged in fluids, as, for
instance, various species of Mucor, Ustilago, Exoascus, and numerous
others. Ascomycetes, and Basidiomycetes as well, are known to form
budding cells, and it was thought that the yeasts of alcoholic fermentation
are merely reduced forms of these higher fungi, which have become
habituated to the budding condition—a conclusion supported by Hansen’s
discovery that a true Saccharomyces can develop a feeble, but a true,
mycelium.
constant types of pure yeasts, each possessing its own peculiar properties.
One consequence of Hansen’s labours was that it now became possible for
every brewer to work with a yeast of uniform type instead of with
haphazard mixtures, in which serious disease forms might predominate and
injure the beer. Among other things made clear was that a true yeast may
have a mycelial stage of development. Furthermore, there is the influence
exercised by the nucleus of the yeast cell. Many other points of interest
arose out of these investigations; one was, that many higher fungi can
assume a yeast-like stage of development if submerged in fluids, as, for
instance, various species of Mucor, Ustilago, Exoascus, and numerous
others. Ascomycetes, and Basidiomycetes as well, are known to form
budding cells, and it was thought that the yeasts of alcoholic fermentation
are merely reduced forms of these higher fungi, which have become
habituated to the budding condition—a conclusion supported by Hansen’s
discovery that a true Saccharomyces can develop a feeble, but a true,
mycelium.
Page 454
Fig. 279.—Saccharomyces and Moulds.
1. Section from a tomato, showing spores growing from cuticle; 2. Portion
detached to show budding-out process; 3. Lateral view of spore sac with oospores
issuing forth; 4. Apiculated ferment spores; 6 and 7. Mycoderma cerivisiæ in
different stages of growth, as seen on wine bottles; 8 and 9. Torulæ diabeticæ,
torulæ and fission spores.
“This view has been entirely confirmed by an inquiry into the mode of
brewing saké by the Japanese, by the aid of the Aspergillus fungus. Further
researches established the fact that other forms of fungi, e.g., those on the
surface of fruits, developed endogenous spores, which cause alcoholic
fermentation. More recently, and by further experimental inquiry, partly by
pure cultures of separate forms, and partly by well-devised cultures on
ripening fruits still attached to the plant but imprisoned in sterilised glass
vessels, it has been found that yeast and moulds are separate forms, not
1. Section from a tomato, showing spores growing from cuticle; 2. Portion
detached to show budding-out process; 3. Lateral view of spore sac with oospores
issuing forth; 4. Apiculated ferment spores; 6 and 7. Mycoderma cerivisiæ in
different stages of growth, as seen on wine bottles; 8 and 9. Torulæ diabeticæ,
torulæ and fission spores.
“This view has been entirely confirmed by an inquiry into the mode of
brewing saké by the Japanese, by the aid of the Aspergillus fungus. Further
researches established the fact that other forms of fungi, e.g., those on the
surface of fruits, developed endogenous spores, which cause alcoholic
fermentation. More recently, and by further experimental inquiry, partly by
pure cultures of separate forms, and partly by well-devised cultures on
ripening fruits still attached to the plant but imprisoned in sterilised glass
vessels, it has been found that yeast and moulds are separate forms, not
Page 455
genetically connected, but merely associated in nature, as are so many other
forms of yeasts, bacteria, and moulds. Further, Hansen has discovered that
several yeasts furnish quite distinct races or varieties in different breweries
in various parts of the world, so that we cannot avoid the conclusion that
their race characteristics have been impressed on the cells by the continued
action of the conditions of culture to which they have so long been exposed
—they are, in fact, domesticated races.”
The environments of yeasts are peculiar. Sauer found that a given variety of
yeast, whose activity is normally inhibited when the alcohol attains a
certain degree of concentration in the liquid, can be induced to go on
fermenting until a higher degree is attained by the addition of a certain
lactic acid bacterium. The latter, indeed, appears to prepare the way for the
yeast. It has been shown, also, that damage may be done to beers and wines
by allowing plant germs to gain access with the yeast; there are, too, several
forms of yeast that are inimical to the action of the required fermentation.
Other researches show that associated yeasts may ferment better than any
single yeast, and such symbiotic action of two yeasts of high fermenting
power has given better results than either alone. English ginger-beer
furnishes a curious symbiotic association of two organisms—a true yeast
and a true bacterium—so closely united that the yeast cells become
imprisoned in the gelatinous meshes of the bacterium; and it is a curious
fact that this symbiotic union of yeast and bacterium ferments is far more
energetic than either when used alone, and the product is different, large
quantities of lactic and carbonic acids being formed, and little or no alcohol.
Many years ago I gave an account of similar curious symbiotic results
obtained by introducing into a wort-infusion a small proportion of German
yeast, an artificial product composed of honey, malt, and a certain
proportion of spontaneously-fermented wheat flour. This, to my
astonishment, produced ten per cent. more alcohol than any of its
congeners, and did not so soon exhaust itself as brewer’s yeast.54
In the hephir used in Europe for fermenting milk, another symbiotic
association of yeast and a bacterium, it is seen that in this process no less
than four distinct organisms are concerned. I have already instanced the
fermentation of rice to produce saké, which is first acted upon by an
forms of yeasts, bacteria, and moulds. Further, Hansen has discovered that
several yeasts furnish quite distinct races or varieties in different breweries
in various parts of the world, so that we cannot avoid the conclusion that
their race characteristics have been impressed on the cells by the continued
action of the conditions of culture to which they have so long been exposed
—they are, in fact, domesticated races.”
The environments of yeasts are peculiar. Sauer found that a given variety of
yeast, whose activity is normally inhibited when the alcohol attains a
certain degree of concentration in the liquid, can be induced to go on
fermenting until a higher degree is attained by the addition of a certain
lactic acid bacterium. The latter, indeed, appears to prepare the way for the
yeast. It has been shown, also, that damage may be done to beers and wines
by allowing plant germs to gain access with the yeast; there are, too, several
forms of yeast that are inimical to the action of the required fermentation.
Other researches show that associated yeasts may ferment better than any
single yeast, and such symbiotic action of two yeasts of high fermenting
power has given better results than either alone. English ginger-beer
furnishes a curious symbiotic association of two organisms—a true yeast
and a true bacterium—so closely united that the yeast cells become
imprisoned in the gelatinous meshes of the bacterium; and it is a curious
fact that this symbiotic union of yeast and bacterium ferments is far more
energetic than either when used alone, and the product is different, large
quantities of lactic and carbonic acids being formed, and little or no alcohol.
Many years ago I gave an account of similar curious symbiotic results
obtained by introducing into a wort-infusion a small proportion of German
yeast, an artificial product composed of honey, malt, and a certain
proportion of spontaneously-fermented wheat flour. This, to my
astonishment, produced ten per cent. more alcohol than any of its
congeners, and did not so soon exhaust itself as brewer’s yeast.54
In the hephir used in Europe for fermenting milk, another symbiotic
association of yeast and a bacterium, it is seen that in this process no less
than four distinct organisms are concerned. I have already instanced the
fermentation of rice to produce saké, which is first acted upon by an
Page 456
Aspergillus that converts the starch into sugar and an associated yeast, and
this is also shown to be a distinct fungus, symbiotically associated in the
conversion. “Starting, then, from the fact that the constitution of the
medium profoundly affects the physiological action of the fungus, there can
be nothing surprising in the discovery that the fungus is more active in a
medium which has been favourably altered by an associated organism,
whether the latter aids the fungus by directly altering the medium, or by
ridding it of products of excretion, or by adding gaseous or other body. It is
not difficult to see, then, that natural selection will aid in the perpetuation of
the symbiosis, and in cases like that of the ginger-beer plant it is extremely
difficult to get the two organisms apart, a difficulty similar to that in the
case of the soredia of lichens.”
Buchner discovered that by means of extreme pressure a something can be
extracted from yeast which at once decomposes sugar into alcohol and
carbon-dioxide. This something is regarded as a kind of incomplete
protoplasm—a body, as we have already seen, composed of proteid—and in
a structural condition somewhere between that of true soluble enzymes like
invertin and a complete living protoplasm. This reminds me of an older
experiment of mine, the immediate conversion of cane-sugar into grape-
sugar. If we take two parts of white sugar and rub it up in a mortar with one
part of a perfectly dry solid, the German yeast before spoken of, it is
immediately transformed as if by magic into a flowing liquid mass—a
syrup. This process of forming “invert sugar” can be watched under the
microscope; the liberation of carbonic acid gas in large bubbles is seen to
go on simultaneously with the assimilation of the dextrose, and the breaking
up of the crystals of sugar; the cell at the same time increasing in size as
well as in refractive power; a curious state of activity appears to be going
on in the small mass, which is very interesting to watch throughout.
However, the enzymes of Buchner are probably bits off the protoplasm, as
it were, and so the essentials of the theory of fermentation remain, the
immediate agent being not that of protoplasm itself, but of something made
by or broken off from it. Enzymes, or similar bodies, are known to be very
common in plants, and the suspicion that fungi do much work with their aid
is abundantly confirmed. It seems, indeed, that there are a whole series of
these bodies which have the power of carrying over oxygen to other bodies,
this is also shown to be a distinct fungus, symbiotically associated in the
conversion. “Starting, then, from the fact that the constitution of the
medium profoundly affects the physiological action of the fungus, there can
be nothing surprising in the discovery that the fungus is more active in a
medium which has been favourably altered by an associated organism,
whether the latter aids the fungus by directly altering the medium, or by
ridding it of products of excretion, or by adding gaseous or other body. It is
not difficult to see, then, that natural selection will aid in the perpetuation of
the symbiosis, and in cases like that of the ginger-beer plant it is extremely
difficult to get the two organisms apart, a difficulty similar to that in the
case of the soredia of lichens.”
Buchner discovered that by means of extreme pressure a something can be
extracted from yeast which at once decomposes sugar into alcohol and
carbon-dioxide. This something is regarded as a kind of incomplete
protoplasm—a body, as we have already seen, composed of proteid—and in
a structural condition somewhere between that of true soluble enzymes like
invertin and a complete living protoplasm. This reminds me of an older
experiment of mine, the immediate conversion of cane-sugar into grape-
sugar. If we take two parts of white sugar and rub it up in a mortar with one
part of a perfectly dry solid, the German yeast before spoken of, it is
immediately transformed as if by magic into a flowing liquid mass—a
syrup. This process of forming “invert sugar” can be watched under the
microscope; the liberation of carbonic acid gas in large bubbles is seen to
go on simultaneously with the assimilation of the dextrose, and the breaking
up of the crystals of sugar; the cell at the same time increasing in size as
well as in refractive power; a curious state of activity appears to be going
on in the small mass, which is very interesting to watch throughout.
However, the enzymes of Buchner are probably bits off the protoplasm, as
it were, and so the essentials of the theory of fermentation remain, the
immediate agent being not that of protoplasm itself, but of something made
by or broken off from it. Enzymes, or similar bodies, are known to be very
common in plants, and the suspicion that fungi do much work with their aid
is abundantly confirmed. It seems, indeed, that there are a whole series of
these bodies which have the power of carrying over oxygen to other bodies,
Page 457
and so bringing about oxidations of a peculiar character. These curious
enzymes were first observed owing to studies on the changes which wine
and plant juice undergo when exposed to the action of the oxygen of the air.
The browning of cut apples is known to be due to the action of an oxydase,
that is, an oxygen carrying ferment, and the same is claimed for the deep
colouring of certain lacs obtained from the juice of plants, such as
Anacardiaceæ, which are pale and transparent when fresh drawn, but which
gradually darken in colour on exposure to the air. Oxydases have been
isolated from beets, dahlia, potato-tubers, and several other plants. This fact
explains a phenomenon known to botanists, and partly explained by
Schönbein as far back as 1868, that if certain fungi (e.g., Boletus beridies)
are broken or bruised, the yellow or white flesh at once turns blue; this
action is now traced to the presence in the cell sap of an oxydase.
It is the diastatic activity of Aspergillus which is utilised in the making of
saké from rice, and in the preparation of soy from the soja bean in Japan.
Katz has recently tested the diastatic activity of Aspergillus, of Penicillium,
and of Bacterium megatherium, in the presence of large and small quantities
of sugar, and found all are able to produce not only diastase, but also other
enzymes; as the sugar accumulates the diastase formed diminishes, whereas
the accumulation of other carbo-hydrates produces no such effect. Harting’s
investigation on the destruction of timber by fungi derives new interest
from the discovery of an emulsion-like enzyme in many such wood-
destroying forms, which splits up glucosides, amygdalin, and other
substances into sugar, and that hyphæ feed on other carbo-hydrates. The
fact, also, that Aspergillus can form inverts of the sucrase and maltase
types, as well as emulsin, inulate, and diastase, according to circumstances
of nutrition, will explain why this fungus can grow on almost any organic
substance it may happen to alight upon. The secretion of special enzymes
by fungi has a further interest just now, for recent investigations promise to
bring us much nearer to an understanding of the phenomena of parasitism
than it was possible when I was at work upon them some forty or fifty years
ago.
It was De Bary who impelled botanists to abandon older methods, and he
who laid the foundation of modern mycology. Later on he pointed out that
enzymes were first observed owing to studies on the changes which wine
and plant juice undergo when exposed to the action of the oxygen of the air.
The browning of cut apples is known to be due to the action of an oxydase,
that is, an oxygen carrying ferment, and the same is claimed for the deep
colouring of certain lacs obtained from the juice of plants, such as
Anacardiaceæ, which are pale and transparent when fresh drawn, but which
gradually darken in colour on exposure to the air. Oxydases have been
isolated from beets, dahlia, potato-tubers, and several other plants. This fact
explains a phenomenon known to botanists, and partly explained by
Schönbein as far back as 1868, that if certain fungi (e.g., Boletus beridies)
are broken or bruised, the yellow or white flesh at once turns blue; this
action is now traced to the presence in the cell sap of an oxydase.
It is the diastatic activity of Aspergillus which is utilised in the making of
saké from rice, and in the preparation of soy from the soja bean in Japan.
Katz has recently tested the diastatic activity of Aspergillus, of Penicillium,
and of Bacterium megatherium, in the presence of large and small quantities
of sugar, and found all are able to produce not only diastase, but also other
enzymes; as the sugar accumulates the diastase formed diminishes, whereas
the accumulation of other carbo-hydrates produces no such effect. Harting’s
investigation on the destruction of timber by fungi derives new interest
from the discovery of an emulsion-like enzyme in many such wood-
destroying forms, which splits up glucosides, amygdalin, and other
substances into sugar, and that hyphæ feed on other carbo-hydrates. The
fact, also, that Aspergillus can form inverts of the sucrase and maltase
types, as well as emulsin, inulate, and diastase, according to circumstances
of nutrition, will explain why this fungus can grow on almost any organic
substance it may happen to alight upon. The secretion of special enzymes
by fungi has a further interest just now, for recent investigations promise to
bring us much nearer to an understanding of the phenomena of parasitism
than it was possible when I was at work upon them some forty or fifty years
ago.
It was De Bary who impelled botanists to abandon older methods, and he
who laid the foundation of modern mycology. Later on he pointed out that
Page 458
when the infecting germinal tube of a fungus enters a plant-cell, two
phenomena must be taken into account, the penetration of the cell-walls and
tissues, and the attraction which causes the tips of the growing hypha to
face and penetrate these obstacles, instead of gliding over them in the lines
of apparent least resistance. The further development of these two factors
shows that in the successful attack of a parasitic plant on its victim or host
these fungi can excrete cellulose-dissolving enzymes, and that they have the
power of destroying lignine. Zopf has also furnished examples of fungi
which can consume fats. There is, however, one other connection in which
these observations on enzymes in the plant-cell promise to be of
considerable importance, viz., the remarkable action of certain rays of the
solar light on bacteria. It has been known for some time past that if bacteria
in a nutrient liquid are exposed to sunlight they quickly die. The further
researches of Professor Marshall Ward and other workers in the same
direction have brought out the fact that it is really the light rays, and not
high temperatures, that it is especially the blue-violet and ultra-violet rays,
which exert the most effective bactericidal action. This proof depended
upon the production of actual photographs in bacteria of the spectrum itself.
Apart from this, the Professor demonstrated that just such spores as those of
anthrax, at the same time pathogenic and highly resistant to heat, succumb
soonest to the action of these cold light-rays, and that under conditions
which preclude their being poisoned by a liquid bath. It is in all probability
the action of these rays of light upon the enzymes, which abound in the
bacterial cells, that bring about their death.
The sun, then, is seen to be our most powerful scavenger, and this
apparently receives confirmation in connection with Martinaud’s
observations, that the yeasts necessary for wine-making are deficient in
numbers and power on grapes exposed to intense light, and to this is due
that better results are obtained in central France as contrasted with those in
the south. “When we reflect, then, that the nature of parasitic fungi, the
actual demonstration of infection by a fungus spore, the transmission of
germs by water and air, the meaning and significance of polymorphism,
heteræcism, symbiosis, had already been rendered clear in the case of fungi,
and that it was by these studies in fermentation, and in the life-history of the
fungus Saccharomyces, that the way was prepared for the ætiology of
phenomena must be taken into account, the penetration of the cell-walls and
tissues, and the attraction which causes the tips of the growing hypha to
face and penetrate these obstacles, instead of gliding over them in the lines
of apparent least resistance. The further development of these two factors
shows that in the successful attack of a parasitic plant on its victim or host
these fungi can excrete cellulose-dissolving enzymes, and that they have the
power of destroying lignine. Zopf has also furnished examples of fungi
which can consume fats. There is, however, one other connection in which
these observations on enzymes in the plant-cell promise to be of
considerable importance, viz., the remarkable action of certain rays of the
solar light on bacteria. It has been known for some time past that if bacteria
in a nutrient liquid are exposed to sunlight they quickly die. The further
researches of Professor Marshall Ward and other workers in the same
direction have brought out the fact that it is really the light rays, and not
high temperatures, that it is especially the blue-violet and ultra-violet rays,
which exert the most effective bactericidal action. This proof depended
upon the production of actual photographs in bacteria of the spectrum itself.
Apart from this, the Professor demonstrated that just such spores as those of
anthrax, at the same time pathogenic and highly resistant to heat, succumb
soonest to the action of these cold light-rays, and that under conditions
which preclude their being poisoned by a liquid bath. It is in all probability
the action of these rays of light upon the enzymes, which abound in the
bacterial cells, that bring about their death.
The sun, then, is seen to be our most powerful scavenger, and this
apparently receives confirmation in connection with Martinaud’s
observations, that the yeasts necessary for wine-making are deficient in
numbers and power on grapes exposed to intense light, and to this is due
that better results are obtained in central France as contrasted with those in
the south. “When we reflect, then, that the nature of parasitic fungi, the
actual demonstration of infection by a fungus spore, the transmission of
germs by water and air, the meaning and significance of polymorphism,
heteræcism, symbiosis, had already been rendered clear in the case of fungi,
and that it was by these studies in fermentation, and in the life-history of the
fungus Saccharomyces, that the way was prepared for the ætiology of
Page 459
bacterial diseases in animals, there should be no doubt as to the mutual
bearings of these matters.”
Industrial uses of Fungi and Saccharomycetes.
There are many industrial processes which are more or less dependent for
success on bacterial fermentations. The subject is young, but the results
already obtained are seen to be of immense importance from a scientific
point of view, and to open up vistas of practical application already being
taken advantage of in commerce, while problems are continually being
raised by the forester, the agriculturist, the gardener, the dairyman, the
brewer, dyer, tanner, and with regard to various industries, which will
eventually confer great advantages in their economic application.
The remarkable discovery made by Alvarez of the bacillus, which converts
a sterilised decoction of the indigo plant into indigo sugar and indigo white,
the latter then oxidising to form the valuable blue dye, whereas the sterile
decoction itself, even in presence of oxygen, forms no indigo, plainly
proves how these minute organisms may be turned to a good account. There
are, however, important points to be determined as to the action of the
fermentation brought about by these enzymes, and the appearance of certain
mysterious diseases in the indigo vats. Again, certain stages in the
preparation of tea and tobacco leaves are found to depend upon very
carefully regulated fermentations, which must be stopped at the right
moment, or the product will be spoilt. Regarding the possible rôle of
bacteria, the West Indian tobacco has a special bacterium, which has been
isolated and found to play a very important part in its flavour. Every
botanist knows that flax and hemp are the best fibres of Linum and
Cannabis respectively, separated by steeping in water until the middle
lamella is destroyed and the fibres isolated; but it is not so well known that
not every water is suitable for this “retting” or steeping process; and for a
long time this was as much a mystery as why some waters are so much
better than others for brewing. Quite recently Fribes has succeeded in
isolating the bacillus upon which the dissolution of the middle lamella
depends. This investigation brought out other interesting details as to the
reaction produced by living micro-organisms, and which can be utilised in
bearings of these matters.”
Industrial uses of Fungi and Saccharomycetes.
There are many industrial processes which are more or less dependent for
success on bacterial fermentations. The subject is young, but the results
already obtained are seen to be of immense importance from a scientific
point of view, and to open up vistas of practical application already being
taken advantage of in commerce, while problems are continually being
raised by the forester, the agriculturist, the gardener, the dairyman, the
brewer, dyer, tanner, and with regard to various industries, which will
eventually confer great advantages in their economic application.
The remarkable discovery made by Alvarez of the bacillus, which converts
a sterilised decoction of the indigo plant into indigo sugar and indigo white,
the latter then oxidising to form the valuable blue dye, whereas the sterile
decoction itself, even in presence of oxygen, forms no indigo, plainly
proves how these minute organisms may be turned to a good account. There
are, however, important points to be determined as to the action of the
fermentation brought about by these enzymes, and the appearance of certain
mysterious diseases in the indigo vats. Again, certain stages in the
preparation of tea and tobacco leaves are found to depend upon very
carefully regulated fermentations, which must be stopped at the right
moment, or the product will be spoilt. Regarding the possible rôle of
bacteria, the West Indian tobacco has a special bacterium, which has been
isolated and found to play a very important part in its flavour. Every
botanist knows that flax and hemp are the best fibres of Linum and
Cannabis respectively, separated by steeping in water until the middle
lamella is destroyed and the fibres isolated; but it is not so well known that
not every water is suitable for this “retting” or steeping process; and for a
long time this was as much a mystery as why some waters are so much
better than others for brewing. Quite recently Fribes has succeeded in
isolating the bacillus upon which the dissolution of the middle lamella
depends. This investigation brought out other interesting details as to the
reaction produced by living micro-organisms, and which can be utilised in
Page 460
deciding questions of plant chemistry too subtile for testing with ordinary
re-agents. One other important fact connected with these researches is that
botanists have now discarded the view that the middle lamella of the plants
referred to is composed of cellulose, and know that it consists of pectin
compounds. Fribes’ anærobic bacillus is found to dissolve and destroy
pectins and pectinates, but does not touch cellulose or gum. It is well known
that the steeping of skins in water in preparation for tanning involves
bacterial action, owing to which the hair and epidermal coverings are
removed, but it also appears that in the process of swelling the limed skins,
the gases evolved in the substance of the tissues, and the evolution of which
causes the swelling and loosens the fibre so that the tanning solutions may
penetrate, are due to a particular fermentation caused by a bacterium,
which, according to some investigators, is identical with a lactic ferment
introduced by the pine bark, and which is responsible for the advantageous
acidification of the tanning solutions.
Hay is made in different ways, and in those where a “spontaneous” heating
process is resorted to the fermentation is no doubt dependent upon the
presence of thermogenic bacteria. But probably no other subject has
attained to so much importance as the bacteriology of the dairy: the study of
the bacteria found in milk, butter, and cheese in their various forms.
Of milk, especially, much has been written and said as a disease-
transmitting medium, and with every good reason, and, if the statement of a
Continental authority may be accepted that each time we eat a slice of bread
and butter we devour a number of bacteria equal to the population of
Europe, we have sure grounds for seeking for further information as to what
these bacteria are and what they are doing. And similarly so with cheese,
which teems with millions of these minute organisms.
“Some few years ago it was found that the peculiar aroma of butter was due
to a bacterium. There are two species of bacteria, one of which develops an
exquisite flavour and aroma, but the butter keeps badly, while the other
develops less aroma, but the butter keeps better. In America, however, they
have isolated and distributed pure cultures of a particular butter bacillus
which develops the famous ‘June’ flavour, hitherto only met with in the
butter made in a certain district during a short season of the year. This fine-
re-agents. One other important fact connected with these researches is that
botanists have now discarded the view that the middle lamella of the plants
referred to is composed of cellulose, and know that it consists of pectin
compounds. Fribes’ anærobic bacillus is found to dissolve and destroy
pectins and pectinates, but does not touch cellulose or gum. It is well known
that the steeping of skins in water in preparation for tanning involves
bacterial action, owing to which the hair and epidermal coverings are
removed, but it also appears that in the process of swelling the limed skins,
the gases evolved in the substance of the tissues, and the evolution of which
causes the swelling and loosens the fibre so that the tanning solutions may
penetrate, are due to a particular fermentation caused by a bacterium,
which, according to some investigators, is identical with a lactic ferment
introduced by the pine bark, and which is responsible for the advantageous
acidification of the tanning solutions.
Hay is made in different ways, and in those where a “spontaneous” heating
process is resorted to the fermentation is no doubt dependent upon the
presence of thermogenic bacteria. But probably no other subject has
attained to so much importance as the bacteriology of the dairy: the study of
the bacteria found in milk, butter, and cheese in their various forms.
Of milk, especially, much has been written and said as a disease-
transmitting medium, and with every good reason, and, if the statement of a
Continental authority may be accepted that each time we eat a slice of bread
and butter we devour a number of bacteria equal to the population of
Europe, we have sure grounds for seeking for further information as to what
these bacteria are and what they are doing. And similarly so with cheese,
which teems with millions of these minute organisms.
“Some few years ago it was found that the peculiar aroma of butter was due
to a bacterium. There are two species of bacteria, one of which develops an
exquisite flavour and aroma, but the butter keeps badly, while the other
develops less aroma, but the butter keeps better. In America, however, they
have isolated and distributed pure cultures of a particular butter bacillus
which develops the famous ‘June’ flavour, hitherto only met with in the
butter made in a certain district during a short season of the year. This fine-
Page 461
flavoured butter is now constantly manufactured in a hundred American
dairies; and the manufacture of pure butter with a constant flavour has
become a matter of certainty.
“Properly considered, the manufacture of cheese is a form of ‘microscopic
gardening’ even more complex and more horticultural in nature than the
brewing of beer. From the first moment, when the cheesemaker guards and
cools his milk, till his stock is ready he is doing his best to keep down the
growth of micro-organisms rushing about to take possession of his milk. He
therefore coagulates it with rennet—an enzyme of animals, but also, as we
have seen, common in plants—and the curd thus prepared is simply treated
as a medium, on which he grows certain fungi and bacteria, with every
needed precaution for favouring their development, and protecting them
against the inroads of other pests and against unsuitable temperature,
moisture, and access of light. Having succeeded in growing the right kind
of plants on his curd, his art then demands that he shall stop their growth at
the critical moment, and his cheese is ready for market.
“Furthermore, the particular flavour and peculiar odours of cheeses, as
Camembert, Stilton, and Roquefort, have to be obtained, and this is secured,
for instance, by cultivating a certain fungus, Penicillium, on bread, and
purposely adding it to Roquefort. This is found to destroy the lactic and
other acids, and so enables certain bacteria in the cheese to set to work and
further change the medium; whereas in another kind of cheese the object is
to prevent this fungus paving the way for these bacteria. Another kind of
bacillus has been discovered which gives a peculiar clover aroma to certain
cheeses.
“It is thought that more definite results will be obtained by the investigation
of the manufacture of the vegetable cheeses of China and Japan, which are
made by exposing the beans of the leguminous plant, Glycine—termed
soja-beans—to bacterial fermentations in warm cellars with or without
certain mould-fungi. Several kinds of bean-cheeses are made in this way,
known by special names. They all depend upon the peculiar decompositions
of the tissues of the cotyledons of the soja-beans, which contain 35 to 40
per cent. of proteids and quantities of fatty matter. The softened beans are
first rendered mouldy, and the interpenetrating hyphæ render the contents
dairies; and the manufacture of pure butter with a constant flavour has
become a matter of certainty.
“Properly considered, the manufacture of cheese is a form of ‘microscopic
gardening’ even more complex and more horticultural in nature than the
brewing of beer. From the first moment, when the cheesemaker guards and
cools his milk, till his stock is ready he is doing his best to keep down the
growth of micro-organisms rushing about to take possession of his milk. He
therefore coagulates it with rennet—an enzyme of animals, but also, as we
have seen, common in plants—and the curd thus prepared is simply treated
as a medium, on which he grows certain fungi and bacteria, with every
needed precaution for favouring their development, and protecting them
against the inroads of other pests and against unsuitable temperature,
moisture, and access of light. Having succeeded in growing the right kind
of plants on his curd, his art then demands that he shall stop their growth at
the critical moment, and his cheese is ready for market.
“Furthermore, the particular flavour and peculiar odours of cheeses, as
Camembert, Stilton, and Roquefort, have to be obtained, and this is secured,
for instance, by cultivating a certain fungus, Penicillium, on bread, and
purposely adding it to Roquefort. This is found to destroy the lactic and
other acids, and so enables certain bacteria in the cheese to set to work and
further change the medium; whereas in another kind of cheese the object is
to prevent this fungus paving the way for these bacteria. Another kind of
bacillus has been discovered which gives a peculiar clover aroma to certain
cheeses.
“It is thought that more definite results will be obtained by the investigation
of the manufacture of the vegetable cheeses of China and Japan, which are
made by exposing the beans of the leguminous plant, Glycine—termed
soja-beans—to bacterial fermentations in warm cellars with or without
certain mould-fungi. Several kinds of bean-cheeses are made in this way,
known by special names. They all depend upon the peculiar decompositions
of the tissues of the cotyledons of the soja-beans, which contain 35 to 40
per cent. of proteids and quantities of fatty matter. The softened beans are
first rendered mouldy, and the interpenetrating hyphæ render the contents
Page 462
accessible to certain bacteria, which peptonise and otherwise alter them.
There is the further question of the manufacture of vinegar by fermentation,
of the preparation of soy from a brine extract of mouldy and fermented
soja-beans, of bread-making, and other equally interesting manufactures.”
Results of De Bary’s Investigations in Parasitism.
“When the idea of parasitism was rendered definite by the fundamental
distinction drawn by De Bary between a parasite and a saprophyte, it soon
became evident that some further distinction must be made between
obligate facultative parasites and saprophytes respectively. De Bary, when
he proposed these terms for adoption, was clearly alive to the existence of
transitions which we now know to be numerous and so gradual in character
that we can no longer define any such physiological groups. Twenty years
ago penicillium and mucor would have been regarded as saprophytes of the
most obligate type, but we now know that under certain circumstances these
fungi can become parasites, and the borderland between facultative
parasites and saprophytes on the one hand, and between the former and true
parasites on the other, can no longer be recognised.”
In 1866 the germ of an idea was sown which has taken root and extended.
De Bary pointed out that in the case of lichens we have either a fungus
parasite on an algæ, or else certain organisms hitherto accepted as algæ are
merely incomplete forms.
“In 1879 the same observer definitely launched the new hypothesis of
symbiosis. The word itself is due to Frank, who, in a valuable paper on the
biology of the thallus of certain lichens, very clearly set forth the existence
of various stages of life in common among all the lower forms of plants.
The details of these matters are now principally of historical interest. We
now know that lichens are dual organisms, composed of various algæ,
symbiotic with Ascomycetes, with Basidiomycetes, and, as Massee has
shown, even with Gastromycetes. The soil contains also bacterio-lichens.
Hence arose a new biological idea—that a fungus may be in such nicely-
balanced relationship with the host from which it derives its sustenance,
that it may be attended with nearly equal advantage to both.
There is the further question of the manufacture of vinegar by fermentation,
of the preparation of soy from a brine extract of mouldy and fermented
soja-beans, of bread-making, and other equally interesting manufactures.”
Results of De Bary’s Investigations in Parasitism.
“When the idea of parasitism was rendered definite by the fundamental
distinction drawn by De Bary between a parasite and a saprophyte, it soon
became evident that some further distinction must be made between
obligate facultative parasites and saprophytes respectively. De Bary, when
he proposed these terms for adoption, was clearly alive to the existence of
transitions which we now know to be numerous and so gradual in character
that we can no longer define any such physiological groups. Twenty years
ago penicillium and mucor would have been regarded as saprophytes of the
most obligate type, but we now know that under certain circumstances these
fungi can become parasites, and the borderland between facultative
parasites and saprophytes on the one hand, and between the former and true
parasites on the other, can no longer be recognised.”
In 1866 the germ of an idea was sown which has taken root and extended.
De Bary pointed out that in the case of lichens we have either a fungus
parasite on an algæ, or else certain organisms hitherto accepted as algæ are
merely incomplete forms.
“In 1879 the same observer definitely launched the new hypothesis of
symbiosis. The word itself is due to Frank, who, in a valuable paper on the
biology of the thallus of certain lichens, very clearly set forth the existence
of various stages of life in common among all the lower forms of plants.
The details of these matters are now principally of historical interest. We
now know that lichens are dual organisms, composed of various algæ,
symbiotic with Ascomycetes, with Basidiomycetes, and, as Massee has
shown, even with Gastromycetes. The soil contains also bacterio-lichens.
Hence arose a new biological idea—that a fungus may be in such nicely-
balanced relationship with the host from which it derives its sustenance,
that it may be attended with nearly equal advantage to both.
Page 463
“In the humus of forests we find the roots of beeches and other Cupuliferæ
(willows, pines, and so forth) clothed with a dense mantle of hyphæ, and
swollen into fleshlike masses of mycorhiza. In similar soils, and in
moorlands, which abound in the slowly decomposing root-fibres and other
vegetable remains so characteristic of these soils, the roots of orchids,
heaths, gentians, &c., are similarly provided with fungi, the hyphæ of which
penetrate further into the tissues, and even send haustoria into the living
cells, but without injuring them. As observations multiplied it became clear
that the mycorhiza, or fungus-root, was not to be dismissed as a mere case
of roots affected by parasites, but that a symbiotic union, comparable to that
of the lichens, exists, and we must assume that both tree and fungus derive
benefit from the connection.
Fig. 280.—Fine Section through Truffle.
a. Asci filled with spores; b. Mycelia, × 250.
“Frank stated, as the result of his experimental research, that seedling
forest-trees cannot be grown in sterilised soil, where their roots are
(willows, pines, and so forth) clothed with a dense mantle of hyphæ, and
swollen into fleshlike masses of mycorhiza. In similar soils, and in
moorlands, which abound in the slowly decomposing root-fibres and other
vegetable remains so characteristic of these soils, the roots of orchids,
heaths, gentians, &c., are similarly provided with fungi, the hyphæ of which
penetrate further into the tissues, and even send haustoria into the living
cells, but without injuring them. As observations multiplied it became clear
that the mycorhiza, or fungus-root, was not to be dismissed as a mere case
of roots affected by parasites, but that a symbiotic union, comparable to that
of the lichens, exists, and we must assume that both tree and fungus derive
benefit from the connection.
Fig. 280.—Fine Section through Truffle.
a. Asci filled with spores; b. Mycelia, × 250.
“Frank stated, as the result of his experimental research, that seedling
forest-trees cannot be grown in sterilised soil, where their roots are
Page 464
prevented from forming mycorhiza; and he concluded that the fungus
conveys organic materials to the roots, which it obtains by breaking down
the leaf-mould and decaying plant remains, together with water and
minerals from the soil, and plays the especial part of a nitrogen-catching
apparatus. In return for this import service the root pays a tax to the fungus
by sparing it certain of its tissue contents. It is a curious fact then that the
mycorhiza is only formed where humus or vegetable mould abounds.”
These instructive investigations offer an intelligible explanation of the
growth of that well-known subterranean fungus, the truffle (Tuber
cibarium), the microscopic appearances of a section of which formed the
subject of a paper I contributed to “The Popular Science Review” some
years ago (1862). The fungus, as will be seen by the fine section cut through
a truffle, Fig. 280, consists of flocculent filaments, which in the first
instance cover the ground at the fall of the leaf in autumn, under oak or
beech trees, the hyphæ of which penetrate the ground, through the humid
soil to the root-hairs of the tree. Filaments (mycelia) are again given off
which terminate in asci or sacs filled with minute spores of about 1⁄2500th of
an inch in size, while the interspaces are filled up by mycelia, that become
consolidated into a firm nut-like body.
What happens, then, is this: Trees and plants with normal roots and root-
hairs, when growing in ordinary soil, can adapt their roots to life in a soil
heavily charged with humus only by contracting symbiotic association with
the fungus and paying the tax demanded by the latter in return for its
supplies and services. If this adaptation is impossible, and no other suitable
variation is evolved, such trees cannot grow in such soils. The physiological
relations of the root to the fungus must be different in details in the case of
non-green, purely saprophytic, plants, Neottia, Monotropa, &c., and in that
of green plants like Erica, Fagus, and Pinus. It is, however, a well-known
fact that ordinary green plants cannot utilize vegetable débris directly, and
forest trees do so in appearance only, for the fungi, yeasts and bacteria there
are actively decomposing the leaves and other remains. A class of pseudo-
symbiotic organisms are, however, being brought into the foreground,
where the combined action of two symbionts results in the death of or
injury to a third plant, each symbiont alone proving harmless. Some time
ago Vuillemin showed that a disease in olives results from the invasion of a
conveys organic materials to the roots, which it obtains by breaking down
the leaf-mould and decaying plant remains, together with water and
minerals from the soil, and plays the especial part of a nitrogen-catching
apparatus. In return for this import service the root pays a tax to the fungus
by sparing it certain of its tissue contents. It is a curious fact then that the
mycorhiza is only formed where humus or vegetable mould abounds.”
These instructive investigations offer an intelligible explanation of the
growth of that well-known subterranean fungus, the truffle (Tuber
cibarium), the microscopic appearances of a section of which formed the
subject of a paper I contributed to “The Popular Science Review” some
years ago (1862). The fungus, as will be seen by the fine section cut through
a truffle, Fig. 280, consists of flocculent filaments, which in the first
instance cover the ground at the fall of the leaf in autumn, under oak or
beech trees, the hyphæ of which penetrate the ground, through the humid
soil to the root-hairs of the tree. Filaments (mycelia) are again given off
which terminate in asci or sacs filled with minute spores of about 1⁄2500th of
an inch in size, while the interspaces are filled up by mycelia, that become
consolidated into a firm nut-like body.
What happens, then, is this: Trees and plants with normal roots and root-
hairs, when growing in ordinary soil, can adapt their roots to life in a soil
heavily charged with humus only by contracting symbiotic association with
the fungus and paying the tax demanded by the latter in return for its
supplies and services. If this adaptation is impossible, and no other suitable
variation is evolved, such trees cannot grow in such soils. The physiological
relations of the root to the fungus must be different in details in the case of
non-green, purely saprophytic, plants, Neottia, Monotropa, &c., and in that
of green plants like Erica, Fagus, and Pinus. It is, however, a well-known
fact that ordinary green plants cannot utilize vegetable débris directly, and
forest trees do so in appearance only, for the fungi, yeasts and bacteria there
are actively decomposing the leaves and other remains. A class of pseudo-
symbiotic organisms are, however, being brought into the foreground,
where the combined action of two symbionts results in the death of or
injury to a third plant, each symbiont alone proving harmless. Some time
ago Vuillemin showed that a disease in olives results from the invasion of a
Page 465
bacillus (B. oleæ), which can, however, only obtain its way into the tissues
through the passages driven by the hyphæ of a fungus (Chætophoma). The
resulting injury is a sort of burr. This observer also observed the same
bacillus and fungus in the canker burrs of the ash.
Among many similar cases well worth further attention are the invasion of
potato-tubers by bacteria, these making their way down the decaying hyphæ
of pioneer fungi. Professor Marshall Ward has seen tomatoes infected by
similar means, and other facts show that many bacteria which quicken the
rotting of wood are thus led into the tissues by fungi.
Probably no subject in the whole domain of cryptogamic botany has wider
bearings on agricultural science than the study of the flora and changes on
and in manure and soil. Nitrifying bacteria play a very important part by
providing plant life with a most necessary food. They occur in the soil, and
two kinds have been described—the one kind converting ammonia into
nitrous acid, and the other changing nitrous into nitric acid. We are
principally indebted to Winogradsky for our knowledge of these bacteria;
he furnishes instances of the bearing of bacteriological work on this
department of science, and explains, not only the origin of nitre-beds and
deposits, but also the way the ammonia compounds fixed by the soil in the
neighbourhood of the root-hairs are nitrified, and so rendered directly
available to plant life. The investigations of other observers show that the
nitrifying organism is a much more highly-developed and complex form
than had been suspected; that it can be grown on various media, and that it
exhibits considerable polymorphism—i.e., it can be made to branch out and
show other characteristics of a true fungus. “I have,” writes Professor Ward,
“for some time insisted on the fact that river water contains reduced forms
of bacteria—i.e., forms so altered by exposure to light, changes of
temperature, and the low nutritive value of the water, that it is only after
prolonged culture in richer food media that their true nature becomes
apparent.” Strutzer and Hartleb show that the morphological form of the
nitrifying organism can be profoundly altered by just such variations of the
conditions described by Ward, and that it occurs as a branched mycelial
form; as bacilli or bacteria; or as cocci of various dimensions, according to
the conditions.
through the passages driven by the hyphæ of a fungus (Chætophoma). The
resulting injury is a sort of burr. This observer also observed the same
bacillus and fungus in the canker burrs of the ash.
Among many similar cases well worth further attention are the invasion of
potato-tubers by bacteria, these making their way down the decaying hyphæ
of pioneer fungi. Professor Marshall Ward has seen tomatoes infected by
similar means, and other facts show that many bacteria which quicken the
rotting of wood are thus led into the tissues by fungi.
Probably no subject in the whole domain of cryptogamic botany has wider
bearings on agricultural science than the study of the flora and changes on
and in manure and soil. Nitrifying bacteria play a very important part by
providing plant life with a most necessary food. They occur in the soil, and
two kinds have been described—the one kind converting ammonia into
nitrous acid, and the other changing nitrous into nitric acid. We are
principally indebted to Winogradsky for our knowledge of these bacteria;
he furnishes instances of the bearing of bacteriological work on this
department of science, and explains, not only the origin of nitre-beds and
deposits, but also the way the ammonia compounds fixed by the soil in the
neighbourhood of the root-hairs are nitrified, and so rendered directly
available to plant life. The investigations of other observers show that the
nitrifying organism is a much more highly-developed and complex form
than had been suspected; that it can be grown on various media, and that it
exhibits considerable polymorphism—i.e., it can be made to branch out and
show other characteristics of a true fungus. “I have,” writes Professor Ward,
“for some time insisted on the fact that river water contains reduced forms
of bacteria—i.e., forms so altered by exposure to light, changes of
temperature, and the low nutritive value of the water, that it is only after
prolonged culture in richer food media that their true nature becomes
apparent.” Strutzer and Hartleb show that the morphological form of the
nitrifying organism can be profoundly altered by just such variations of the
conditions described by Ward, and that it occurs as a branched mycelial
form; as bacilli or bacteria; or as cocci of various dimensions, according to
the conditions.
Page 466
“These observations, and others made on variations in form
(polymorphism) in other fungi and bacteria, open out a vast field for further
work, and must lead to advancement in our knowledge of these puzzling
organisms; they also help us to explain many inconsistencies in the existing
systems of classification of the so-called ‘species’ of bacteria as determined
by test-tube culture.”
Algæ.—The algals have a special charm for microscopists. I am free to
confess my interest in these organisms, and for several reasons. In this
humid climate of ours they are accessible during the greater part of the year;
they can be found in any damp soil, in bog, moss, and in water—indeed,
wherever the conditions for their existence seem to be at all favourable for
development. Should the soil dry up for a time, when the rain returns algæ
are seen to spring into life and give forth their dormant spores, which once
more resume the circle of formation and propagation. In the earliest stage of
development the spore or spore cell is so very small when in a desiccated
state, that any number may be carried about by the slightest breath of air
and borne away to a great distance. To all such organisms I originally gave
the name of Ærozoa; now recognised as ærobic and anærobic organisms
(Fig. 281).
Fig. 281.—Ærobic Spores × 200.
1. Ærobic fungi caught over a sewer; 2. Fragments of Penicillium spores; 3.
Ærobic fungi taken in the time of the cholera visitation, 1854.
With reference to the ærobic bacteria I have only to add that in addition to
the simple mode of taking them on glass slides smeared over with
glycerine, special forms of æroscopes are now in use for the purpose,
consisting of a small cylinder in which a current of air is produced by an
(polymorphism) in other fungi and bacteria, open out a vast field for further
work, and must lead to advancement in our knowledge of these puzzling
organisms; they also help us to explain many inconsistencies in the existing
systems of classification of the so-called ‘species’ of bacteria as determined
by test-tube culture.”
Algæ.—The algals have a special charm for microscopists. I am free to
confess my interest in these organisms, and for several reasons. In this
humid climate of ours they are accessible during the greater part of the year;
they can be found in any damp soil, in bog, moss, and in water—indeed,
wherever the conditions for their existence seem to be at all favourable for
development. Should the soil dry up for a time, when the rain returns algæ
are seen to spring into life and give forth their dormant spores, which once
more resume the circle of formation and propagation. In the earliest stage of
development the spore or spore cell is so very small when in a desiccated
state, that any number may be carried about by the slightest breath of air
and borne away to a great distance. To all such organisms I originally gave
the name of Ærozoa; now recognised as ærobic and anærobic organisms
(Fig. 281).
Fig. 281.—Ærobic Spores × 200.
1. Ærobic fungi caught over a sewer; 2. Fragments of Penicillium spores; 3.
Ærobic fungi taken in the time of the cholera visitation, 1854.
With reference to the ærobic bacteria I have only to add that in addition to
the simple mode of taking them on glass slides smeared over with
glycerine, special forms of æroscopes are now in use for the purpose,
consisting of a small cylinder in which a current of air is produced by an
Page 467
aspirator and diffused through a glass vessel containing a sterilised fluid.
These are in constant use in all bacteriological laboratories. The results
obtained are transferred to sterilised flasks or tubes as those shown in a
former chapter.
Miquel, who has given considerable attention to the subject of ærobic and
anærobic bacteria, reckons that the number of spores that find their way into
the human system by respiration, even should health be perfectly sound,
may be estimated at 300,000 a day.
One of the most commonly met with forms of micro-organisms is
Leptothrix buccalis. It chiefly finds its nutritive material in the interstices of
the teeth, and is composed of short rods and tufted stems of vigorous
growth, to which the name of Bacillus subtilis has been given (Fig. 282).
Among numerous other fungoid bodies discovered in the mouth, Sarcinæ
have been found. See Plate IX., No. 7.
Fig. 282.—Section of the Mucous Membrane of the Mouth, × 350.
Showing: a. The denser connective tissue; b. Teased out tissue; c. Muscular fibre;
d. Leptothrix buccalis, together with minute forms of bacteria and micrococci; e.
Ascomycetes and starch granules.
These are in constant use in all bacteriological laboratories. The results
obtained are transferred to sterilised flasks or tubes as those shown in a
former chapter.
Miquel, who has given considerable attention to the subject of ærobic and
anærobic bacteria, reckons that the number of spores that find their way into
the human system by respiration, even should health be perfectly sound,
may be estimated at 300,000 a day.
One of the most commonly met with forms of micro-organisms is
Leptothrix buccalis. It chiefly finds its nutritive material in the interstices of
the teeth, and is composed of short rods and tufted stems of vigorous
growth, to which the name of Bacillus subtilis has been given (Fig. 282).
Among numerous other fungoid bodies discovered in the mouth, Sarcinæ
have been found. See Plate IX., No. 7.
Fig. 282.—Section of the Mucous Membrane of the Mouth, × 350.
Showing: a. The denser connective tissue; b. Teased out tissue; c. Muscular fibre;
d. Leptothrix buccalis, together with minute forms of bacteria and micrococci; e.
Ascomycetes and starch granules.
Page 468
The Beggiatoa, a sewage fungus, found by me in the river Lea water of
1884 growing in great profusion, consists chiefly of mycelial threads and a
number of globular, highly refractive bodies, and may be regarded as
evidence of the presence in the water of an abnormal amount of sulphates
which set free a gas, sulphuretted hydrogen, of a dangerous and offensive
character. Another curious body closely allied to Beggiatoa alba is
Cladothrix; this assumes a whitish pellicle on the surface of putrefying
liquids.
These saprophytes obtain nourishment from organic matter; nevertheless
they are not true parasites in the first stage of their existence, during which
they live freely in the water or in damp soil; they, however, become
pathogenic parasites when they penetrate into the tissues of animals, and
necessarily live at the expense of their host.
Fungi, Algæ, Lichens, etc.
1884 growing in great profusion, consists chiefly of mycelial threads and a
number of globular, highly refractive bodies, and may be regarded as
evidence of the presence in the water of an abnormal amount of sulphates
which set free a gas, sulphuretted hydrogen, of a dangerous and offensive
character. Another curious body closely allied to Beggiatoa alba is
Cladothrix; this assumes a whitish pellicle on the surface of putrefying
liquids.
These saprophytes obtain nourishment from organic matter; nevertheless
they are not true parasites in the first stage of their existence, during which
they live freely in the water or in damp soil; they, however, become
pathogenic parasites when they penetrate into the tissues of animals, and
necessarily live at the expense of their host.
Fungi, Algæ, Lichens, etc.
Page 469
Tuffen West, del. Edmund Evans.
Plate I.
Bacteria, as I have said, were for a long time classed with fungi under the
name of Schizomycetes. But the more recent researches into their
organisation, and more especially into their mode of reproduction, show
that they rather more resemble a group of algæ devoid of chlorophyll. Zopf
asserts that the same species of algals may at one time be presented in the
form of a plant living freely in water, or in damp ground, in association with
chlorophyllaceous protoplasm, and at another in the form of a bacterium
devoid of green colouring matter, and receiving nourishment from organic
substances previously elaborated by plants or animals, thus accommodating
itself, according to circumstances, to two very different modes of existence.
Plate I.
Bacteria, as I have said, were for a long time classed with fungi under the
name of Schizomycetes. But the more recent researches into their
organisation, and more especially into their mode of reproduction, show
that they rather more resemble a group of algæ devoid of chlorophyll. Zopf
asserts that the same species of algals may at one time be presented in the
form of a plant living freely in water, or in damp ground, in association with
chlorophyllaceous protoplasm, and at another in the form of a bacterium
devoid of green colouring matter, and receiving nourishment from organic
substances previously elaborated by plants or animals, thus accommodating
itself, according to circumstances, to two very different modes of existence.
Page 470
That widely-distributed single-cell plant, the Palmoglœa macrococca of
Kützing, that spreads itself as a green slime over damp stones, walls, and
other bodies, affords an example. If a small portion be scraped off and
placed on a slip of glass, and examined with a half or a quarter-inch power,
it will be seen to consist of a number of ovoid cells, having a transparent
structureless envelope, nearly filled by granular matter of a greenish colour.
At certain periods this mass divides into two parts, and ultimately the cell
becomes two. Sometimes the cells are united end to end, just as we see
them united in the actively-growing yeast plant; but in this case the growth
is accelerated, apparently, by cold and damp. Another plant belonging to the
same species, the Protococcus pluvialis, is found in every pool of water, the
spores of which must be always floating in the air, since they appear after
every shower of rain.
Protococcus pluvialis is furnished with motile organs—two or more
vibratile flagella passing through perforations in the cell-wall—whereby, at
certain stages, they move rapidly about. The flagella are distinctly seen on
the application of the smallest drop of iodine. The more remarkable of the
several forms presented by the plant is that of naked spores, termed by
Flotow Hæmatococcus porphyrocephalus. These minute bodies are usually
seen to consist of green, red, and colourless granules in equal proportions,
and occupying different portions of the cell. They seem to have some share
in the after subdivision of the cell (Fig. 283). There are also still-cells,
which sub-divide into two, while the motile cells divide into four or eight. It
is not quite clear what becomes of the motile zoospores, B, but as they have
been seen to become encysted, they doubtless have a special function, or
become still-cells under certain circumstances.
It appears that both longitudinal and transverse division of the primordial
cell takes place; and that the vibratile flagella of the parent cell retain to the
last their function and their motion after the primordial cell has become
detached and transformed into an independent secondary cell (Fig. 283, G).
Kützing, that spreads itself as a green slime over damp stones, walls, and
other bodies, affords an example. If a small portion be scraped off and
placed on a slip of glass, and examined with a half or a quarter-inch power,
it will be seen to consist of a number of ovoid cells, having a transparent
structureless envelope, nearly filled by granular matter of a greenish colour.
At certain periods this mass divides into two parts, and ultimately the cell
becomes two. Sometimes the cells are united end to end, just as we see
them united in the actively-growing yeast plant; but in this case the growth
is accelerated, apparently, by cold and damp. Another plant belonging to the
same species, the Protococcus pluvialis, is found in every pool of water, the
spores of which must be always floating in the air, since they appear after
every shower of rain.
Protococcus pluvialis is furnished with motile organs—two or more
vibratile flagella passing through perforations in the cell-wall—whereby, at
certain stages, they move rapidly about. The flagella are distinctly seen on
the application of the smallest drop of iodine. The more remarkable of the
several forms presented by the plant is that of naked spores, termed by
Flotow Hæmatococcus porphyrocephalus. These minute bodies are usually
seen to consist of green, red, and colourless granules in equal proportions,
and occupying different portions of the cell. They seem to have some share
in the after subdivision of the cell (Fig. 283). There are also still-cells,
which sub-divide into two, while the motile cells divide into four or eight. It
is not quite clear what becomes of the motile zoospores, B, but as they have
been seen to become encysted, they doubtless have a special function, or
become still-cells under certain circumstances.
It appears that both longitudinal and transverse division of the primordial
cell takes place; and that the vibratile flagella of the parent cell retain to the
last their function and their motion after the primordial cell has become
detached and transformed into an independent secondary cell (Fig. 283, G).
Page 471
Fig. 283.—Cell Development. (Protococcus pluvialis.)
Protococcus pluvialis, Kützing. Hæmatococcus pluvialis, Flotow. Chlamidococcus
versatilis, A. Braun. Chlamidococcus pluvialis, Flotow and Braun.
A. Division of a simple cell into two, each primordial vesicle having developed a
cellulose envelope; B. Zoospores, having escaped from a cell; C. Division of an
encysted cell into segments; D. Division of another cell, with vibratile flagella
projecting through cell-wall; E. An encysted flagellate cell; F. Division of an
encysted nucleated cell into four parts, with vibratile filaments projecting; G.
Fission of a young cell.
The most striking of the vital phenomena presented by Protococcus is that
of periodicity. Certain forms—for instance, encysted zoospores, of a certain
colour, appear in a given infusion, at first exclusively, then they gradually
diminish, become more and more rare, and finally disappear altogether.
After some time their number again increases, and this may be repeated.
Thus, a cell which at one time presented only still forms at another
contained only motile ones. The same may be said with respect to
segmentation. If a number of motile cells be transferred from a larger vessel
into a smaller one, in the course of a few hours most of them will have
subsided to the bottom, and in the course of the day observed to be on the
point of sub-division. On the following morning division will have become
completed; on the next day the bottom of the vessel will be found covered
with a new generation of self-dividing cells, which, again, will produce
another generation. This regularity, however, is not always observed. The
influence of every change in the external conditions of life upon the plant is
Protococcus pluvialis, Kützing. Hæmatococcus pluvialis, Flotow. Chlamidococcus
versatilis, A. Braun. Chlamidococcus pluvialis, Flotow and Braun.
A. Division of a simple cell into two, each primordial vesicle having developed a
cellulose envelope; B. Zoospores, having escaped from a cell; C. Division of an
encysted cell into segments; D. Division of another cell, with vibratile flagella
projecting through cell-wall; E. An encysted flagellate cell; F. Division of an
encysted nucleated cell into four parts, with vibratile filaments projecting; G.
Fission of a young cell.
The most striking of the vital phenomena presented by Protococcus is that
of periodicity. Certain forms—for instance, encysted zoospores, of a certain
colour, appear in a given infusion, at first exclusively, then they gradually
diminish, become more and more rare, and finally disappear altogether.
After some time their number again increases, and this may be repeated.
Thus, a cell which at one time presented only still forms at another
contained only motile ones. The same may be said with respect to
segmentation. If a number of motile cells be transferred from a larger vessel
into a smaller one, in the course of a few hours most of them will have
subsided to the bottom, and in the course of the day observed to be on the
point of sub-division. On the following morning division will have become
completed; on the next day the bottom of the vessel will be found covered
with a new generation of self-dividing cells, which, again, will produce
another generation. This regularity, however, is not always observed. The
influence of every change in the external conditions of life upon the plant is
Page 472
very remarkable. It is only necessary to pour water from a smaller into a
larger or shallower vessel to at once induce segmentation of cells. The same
phenomenon occurs in other algals; thus Vaucheria almost always develops
zoospores at whatever time of year they may be brought from their natural
habitat into a warm room. Light is conducive to the manifestation of vital
action in the motile spores; they usually collect in great numbers on the
surface of the water, and at that part exposed to the strongest light.
But in the act of propagation, on the contrary, and when about to pass into
the still condition, the motile Protococcus cell seems to shun light, and falls
to the bottom of the vessel. Too strong sunlight, as when concentrated by a
lens, quickly kills the young zoospores. A temperature of undue elevation is
injurious to the development of their vital activity and the formation of the
zoospores. Frost destroys motile, but not still zoospores.55
Stephanosphæra pluvialis is a conspicuous variety of the fresh-water algals,
described by Cohn. It consists of a cell containing eight primordial cells
filled with chlorophyll, uniformly arranged (see Plate I., No. 24 d). The
globular mother-cell rotates, somewhat in the same way as the volvox, by
vibratile flagella, two of which are seen projecting from each cell and
piercing the transparent outer cell wall. Every cell divides first into two,
then four, and lastly eight cells, each one of which again divides into a
number of micro-gonidia, which have a motion within the mother-cell, and
ultimately escape from it. Under certain circumstances each of the eight
young cells is observed to change places in the interior of the cell;
eventually they escape, lose their flagella, form a thicker membrane as at b,
and for a time remain motionless, and sink to the bottom of the vessel in
which they are contained. If the vessel is permitted to become thoroughly
dry, and then again has water poured into it, motile cells reappear; from
which circumstance it is probable that these represent the resting spores of
the plant. When in the condition of greatest activity its division into eight is
perfected during the night, and early in the morning light the young cells
escape and pass through similar changes. It is calculated that in eight days,
under favourable circumstances, 16,777,216 families may be formed from
one resting-cell of Stephanosphæra. In certain of the cells, and at particular
periods, remarkable amœboid bodies (Plate I., No. 24 c) make their
appearance. There is a marked difference between Stephanosphæra and
larger or shallower vessel to at once induce segmentation of cells. The same
phenomenon occurs in other algals; thus Vaucheria almost always develops
zoospores at whatever time of year they may be brought from their natural
habitat into a warm room. Light is conducive to the manifestation of vital
action in the motile spores; they usually collect in great numbers on the
surface of the water, and at that part exposed to the strongest light.
But in the act of propagation, on the contrary, and when about to pass into
the still condition, the motile Protococcus cell seems to shun light, and falls
to the bottom of the vessel. Too strong sunlight, as when concentrated by a
lens, quickly kills the young zoospores. A temperature of undue elevation is
injurious to the development of their vital activity and the formation of the
zoospores. Frost destroys motile, but not still zoospores.55
Stephanosphæra pluvialis is a conspicuous variety of the fresh-water algals,
described by Cohn. It consists of a cell containing eight primordial cells
filled with chlorophyll, uniformly arranged (see Plate I., No. 24 d). The
globular mother-cell rotates, somewhat in the same way as the volvox, by
vibratile flagella, two of which are seen projecting from each cell and
piercing the transparent outer cell wall. Every cell divides first into two,
then four, and lastly eight cells, each one of which again divides into a
number of micro-gonidia, which have a motion within the mother-cell, and
ultimately escape from it. Under certain circumstances each of the eight
young cells is observed to change places in the interior of the cell;
eventually they escape, lose their flagella, form a thicker membrane as at b,
and for a time remain motionless, and sink to the bottom of the vessel in
which they are contained. If the vessel is permitted to become thoroughly
dry, and then again has water poured into it, motile cells reappear; from
which circumstance it is probable that these represent the resting spores of
the plant. When in the condition of greatest activity its division into eight is
perfected during the night, and early in the morning light the young cells
escape and pass through similar changes. It is calculated that in eight days,
under favourable circumstances, 16,777,216 families may be formed from
one resting-cell of Stephanosphæra. In certain of the cells, and at particular
periods, remarkable amœboid bodies (Plate I., No. 24 c) make their
appearance. There is a marked difference between Stephanosphæra and
Page 473
Chlamydococcus, for while in the latter the individual portions of a
primordial cell separate entirely from one another, each developing its own
enveloping membrane, and ultimately escaping as a unicellular individual;
in the former, on the other hand, the eight portions remain for a time living
in companionship.
Volvocineæ.—A fresh-water unicellular plant of singular beauty and interest
to the microscopist is the Volvox globator (Plate I., No. 15). No. 16
represents a portion of another cell, with brownish amœboid bodies
enclosed in the protoplasmic web. It is common to our fresh-water pools,
and attains a diameter of about 1⁄20th or 1⁄30th of an inch. Its movement is
peculiar, a continued roll onwards, or a rotation like that of a top; at other
times it glides along smoothly. When examined under a sufficiently high
power, it is seen to be a hollow sphere, studded with green spots, and
traversed by green threads connecting each of the spots or spores with the
maternal cell. From each of the spores proceed two long flagella, lashing
filaments, which keep the globular body on the move. After a time the
sphere bursts, and the contained sporules issue forth and speedily pass
through a similar stage of development. These interesting cells were long
taken to be animal bodies. Ehrenberg described them as Monads, possessing
a mouth, stomach, and an eye.
The setting free of the young volvox is essentially a process of cell division,
occurring during the warmer periods of the year, and, as Professor Cohn
shows, is a considerable advance upon the simpler conjugation of two
smaller cells in desmids; it more closely resembles that which prevails
among the higher algæ and a large number of cryptogams. As autumn
advances the volvox spherules usually cease to multiply by the formation of
zoosporanges, and certain of their ordinary cells begin to undergo changes
by which they are converted, some into male or sperm-cells, others into
germ-cells, but the greater number appear to remain sterile. Both kinds of
cells at first so nearly resemble each other that it is only when the sperm
cells begin to undergo sub-division that they are seen to be about three
times the size of the sterile cells. Then the primary cell resolves itself into a
cluster of peculiar secondary cells, each consisting of an elongated body
containing an orange-coloured endochrome and a pair of long flagella, as
seen in the antherozoids of the higher cryptogams. As the sperm-cells
primordial cell separate entirely from one another, each developing its own
enveloping membrane, and ultimately escaping as a unicellular individual;
in the former, on the other hand, the eight portions remain for a time living
in companionship.
Volvocineæ.—A fresh-water unicellular plant of singular beauty and interest
to the microscopist is the Volvox globator (Plate I., No. 15). No. 16
represents a portion of another cell, with brownish amœboid bodies
enclosed in the protoplasmic web. It is common to our fresh-water pools,
and attains a diameter of about 1⁄20th or 1⁄30th of an inch. Its movement is
peculiar, a continued roll onwards, or a rotation like that of a top; at other
times it glides along smoothly. When examined under a sufficiently high
power, it is seen to be a hollow sphere, studded with green spots, and
traversed by green threads connecting each of the spots or spores with the
maternal cell. From each of the spores proceed two long flagella, lashing
filaments, which keep the globular body on the move. After a time the
sphere bursts, and the contained sporules issue forth and speedily pass
through a similar stage of development. These interesting cells were long
taken to be animal bodies. Ehrenberg described them as Monads, possessing
a mouth, stomach, and an eye.
The setting free of the young volvox is essentially a process of cell division,
occurring during the warmer periods of the year, and, as Professor Cohn
shows, is a considerable advance upon the simpler conjugation of two
smaller cells in desmids; it more closely resembles that which prevails
among the higher algæ and a large number of cryptogams. As autumn
advances the volvox spherules usually cease to multiply by the formation of
zoosporanges, and certain of their ordinary cells begin to undergo changes
by which they are converted, some into male or sperm-cells, others into
germ-cells, but the greater number appear to remain sterile. Both kinds of
cells at first so nearly resemble each other that it is only when the sperm
cells begin to undergo sub-division that they are seen to be about three
times the size of the sterile cells. Then the primary cell resolves itself into a
cluster of peculiar secondary cells, each consisting of an elongated body
containing an orange-coloured endochrome and a pair of long flagella, as
seen in the antherozoids of the higher cryptogams. As the sperm-cells
Page 474
approach maturity the clusters may be seen to move within them; the
bundles then separate and show an independent active movement while still
within the cavity of the primary cell, and finally escape through a rupture in
the cell-wall, rapidly diffusing themselves as they pass through the cavity.
The germ-cells continue to increase in size without undergoing sub-
division, at first showing large vacuoles in their protoplasm, but
subsequently becoming filled with a darker coloured endochrome. The form
of the cell also changes from its flask-like shape to the globular, and at the
same time seems to acquire a firmer envelope. Over this the swarming
antherozoids diffuse themselves and penetrate the substance to the interior,
and are then lost to view. The product of this fusion, Cohn tells us, is a
reproductive cell, or “oospore,” which speedily becomes enveloped in
another membrane with a thicker external coat, beset with conical-pointed
processes; and now the chlorophyll of the young cell gives place, as in
Palmoglæ, to starch and reddish or orange-coloured, and a more highly
refractive, fluid. As many as forty of such oospores have been counted in a
single sphere of volvox, which then acquires the peculiar appearance
observed by Ehrenberg, and described by him under the name of Volvox
stellatus. The further history of this wonderful spheroid unicellular plant
has been traced out by Kirchner, who found that their germination
commences in the early months of the year—in February—with the
liberation of the spherical endospore from its envelope and its division into
four cells. A remarkable phenomenon has been observed by Dr. Braxton
Hicks—the conversion of an ordinary volvox cell into a moving mass of
protoplasm that bears a striking resemblance to the well-known amœba.
“Towards the end of the autumn the endochrome mass of the volvox
increases to nearly double its ordinary size, but instead of undergoing the
usual sub-division so as to produce a macrogonidium, it loses its colour and
regularity of form, and becomes an irregular mass of colourless protoplasm,
containing a number of brownish granules.” The final change and the
ultimate destination of these curious amœboid bodies have not been
satisfactorily made out, but from other observations on the protoplasmic
contents of the cells of the roots of mosses, which in the course of two
hours become changed into ciliated bodies, it is believed that this is the
mode in which these fragile structures are enabled to retain life and to resist
all the external conditions, such as damp, dryness, and the alternations of
heat and cold.
bundles then separate and show an independent active movement while still
within the cavity of the primary cell, and finally escape through a rupture in
the cell-wall, rapidly diffusing themselves as they pass through the cavity.
The germ-cells continue to increase in size without undergoing sub-
division, at first showing large vacuoles in their protoplasm, but
subsequently becoming filled with a darker coloured endochrome. The form
of the cell also changes from its flask-like shape to the globular, and at the
same time seems to acquire a firmer envelope. Over this the swarming
antherozoids diffuse themselves and penetrate the substance to the interior,
and are then lost to view. The product of this fusion, Cohn tells us, is a
reproductive cell, or “oospore,” which speedily becomes enveloped in
another membrane with a thicker external coat, beset with conical-pointed
processes; and now the chlorophyll of the young cell gives place, as in
Palmoglæ, to starch and reddish or orange-coloured, and a more highly
refractive, fluid. As many as forty of such oospores have been counted in a
single sphere of volvox, which then acquires the peculiar appearance
observed by Ehrenberg, and described by him under the name of Volvox
stellatus. The further history of this wonderful spheroid unicellular plant
has been traced out by Kirchner, who found that their germination
commences in the early months of the year—in February—with the
liberation of the spherical endospore from its envelope and its division into
four cells. A remarkable phenomenon has been observed by Dr. Braxton
Hicks—the conversion of an ordinary volvox cell into a moving mass of
protoplasm that bears a striking resemblance to the well-known amœba.
“Towards the end of the autumn the endochrome mass of the volvox
increases to nearly double its ordinary size, but instead of undergoing the
usual sub-division so as to produce a macrogonidium, it loses its colour and
regularity of form, and becomes an irregular mass of colourless protoplasm,
containing a number of brownish granules.” The final change and the
ultimate destination of these curious amœboid bodies have not been
satisfactorily made out, but from other observations on the protoplasmic
contents of the cells of the roots of mosses, which in the course of two
hours become changed into ciliated bodies, it is believed that this is the
mode in which these fragile structures are enabled to retain life and to resist
all the external conditions, such as damp, dryness, and the alternations of
heat and cold.
Page 475
It would be quite impossible to deny the great similarity there is between
the structure of volvox and that of the motile cell of Protococcus pluvialis.
The influence of reagents will sometimes cause the connecting processes of
the young cells, as in Protococcus, to be drawn back into the central mass,
and the connecting threads are sometimes seen as double lines, or tubular
prolongations of the membrane. At other times they appear to be connected
by star-like prolongations to the parent cell (Plate I., No. 15), presenting an
almost identical appearance with Pediastrum pertusum. Another body
designated by Ehrenberg Sphærosira volvox is an ordinary volvox in a
different stage of development; its only features of dissimilarity being that a
large proportion of the green cells, instead of being single, are double or
quadruple, and that the groups of flagellate cells form by their aggregation
discoid bodies, each furnished with a single flagellum. These clusters
separate themselves from the parent cell, and swim off freely under the
forms which have been designated Uvella and Syncrypta by Ehrenberg. Mr.
Henry Carter, F.R.S., who made a careful investigation of unicellular plants,
described Sphærosira as the male, or spermatic form of volvox.
Among other organisms closely allied to volvox and included in
Volvocineæ, affording the microscopist many interesting transitional forms
in their various modes of fructification, are the Eudorina, still-water
organisms that pass through a similar process of reproduction as the volvox.
In the Pandorina morum, its reproduction is curiously intermediate between
the lower and the higher types; as within each cell is a mulberry-like mass,
composed of cells possessing a definite number of swarm spores, sixteen
usually, which rupture the mother cell, and swim off furnished with a pair
of flagella. A similar process takes place in some of the Confervaceæ and
other fresh-water algæ. The Palmella, again, consist of (Plate I., No. 21)
minute organisms of very simple structure, which grow either on damp
surfaces or in fresh water. The stonework of some of our churches is often
seen to be covered with a species of Palmella, that take the form of an
indefinite slimy film. The “red snow” of Arctic or Alpine regions,
considered to be a species of Protococcus, is frequently placed among
Palmella. A more characteristic form of the P. cruenta is the Hæmatococcus
sanguinis, the whole mass of which is sub-divided by partitions enclosing a
larger or smaller number of cells, which diffuse their granular contents
through the gelatinous mass in which their several changes take place. The
the structure of volvox and that of the motile cell of Protococcus pluvialis.
The influence of reagents will sometimes cause the connecting processes of
the young cells, as in Protococcus, to be drawn back into the central mass,
and the connecting threads are sometimes seen as double lines, or tubular
prolongations of the membrane. At other times they appear to be connected
by star-like prolongations to the parent cell (Plate I., No. 15), presenting an
almost identical appearance with Pediastrum pertusum. Another body
designated by Ehrenberg Sphærosira volvox is an ordinary volvox in a
different stage of development; its only features of dissimilarity being that a
large proportion of the green cells, instead of being single, are double or
quadruple, and that the groups of flagellate cells form by their aggregation
discoid bodies, each furnished with a single flagellum. These clusters
separate themselves from the parent cell, and swim off freely under the
forms which have been designated Uvella and Syncrypta by Ehrenberg. Mr.
Henry Carter, F.R.S., who made a careful investigation of unicellular plants,
described Sphærosira as the male, or spermatic form of volvox.
Among other organisms closely allied to volvox and included in
Volvocineæ, affording the microscopist many interesting transitional forms
in their various modes of fructification, are the Eudorina, still-water
organisms that pass through a similar process of reproduction as the volvox.
In the Pandorina morum, its reproduction is curiously intermediate between
the lower and the higher types; as within each cell is a mulberry-like mass,
composed of cells possessing a definite number of swarm spores, sixteen
usually, which rupture the mother cell, and swim off furnished with a pair
of flagella. A similar process takes place in some of the Confervaceæ and
other fresh-water algæ. The Palmella, again, consist of (Plate I., No. 21)
minute organisms of very simple structure, which grow either on damp
surfaces or in fresh water. The stonework of some of our churches is often
seen to be covered with a species of Palmella, that take the form of an
indefinite slimy film. The “red snow” of Arctic or Alpine regions,
considered to be a species of Protococcus, is frequently placed among
Palmella. A more characteristic form of the P. cruenta is the Hæmatococcus
sanguinis, the whole mass of which is sub-divided by partitions enclosing a
larger or smaller number of cells, which diffuse their granular contents
through the gelatinous mass in which their several changes take place. The
Page 476
albuminoid envelope of these masses is seen to contain parasitic growths,
which have given rise to some discussion, especially when their filaments
are observed to radiate in various directions.
The Oscillariaceæ constitute a genus of Confervaceæ which have always
had very great interest for the microscopist in consequence of their very
remarkable animal-like movements, and from which they derive their
generic name. For more than a century these Bacillaria have excited the
curiosity of all observers without any one having derived more than an
approximate idea of their remarkable rhythmical movements. The frustule
consists of a number of very fine short threads attached together by a
gelatinous sheath, in one species all of equal length. Their backward and
forward movement is of a most singular character; the only other conferva
in which I have seen a motion of a similar kind is the Schizonema. In this
species the frustules are packed together in regular series, the front and side
views being always in the same direction. These several bodies move along
within the filamentous sheath without leaving their respective places. On
carefully following the movement, it is seen at first much extended, and
then more compressed, while the frustules become more linear in their
arrangement, and present a closer resemblance to Bacillaria paradoxa,
augmented by the circumstance that the frustules are seen to move in both
directions. A frustule of Schizonema can move independently of the sheath,
and so will a detached frustule of bacillaria. This peculiar and exceptionally
anomalous phenomenon as that of the movements of bacillaria can hardly
be confined to a solitary species. The movements of the frustules are much
accelerated by warmth and light. The longer filaments of other minute
species only slightly exhibit any motion of the kind, but have peculiar
undulating motions.
Confervaceæ are a genus of algals. The species consist of unbranched
filaments composed of cylindrical or moniliform cells, with starch granules.
Many are vesicular, and all multiply by zoospores generated in the interior
of the plant at the expense of the granular matter. They are, for the most
part, found in fresh water attached or floating, some in salt water, and a few
in both, in colour usually green, but occasionally olive, violet, and red. The
Confervaceæ proper are often divided into four families: 1. Hydrodictidæ;
2. Zygnemidæ; 3. Confervidæ; 4. Chætophoridæ. To the microscopist all the
which have given rise to some discussion, especially when their filaments
are observed to radiate in various directions.
The Oscillariaceæ constitute a genus of Confervaceæ which have always
had very great interest for the microscopist in consequence of their very
remarkable animal-like movements, and from which they derive their
generic name. For more than a century these Bacillaria have excited the
curiosity of all observers without any one having derived more than an
approximate idea of their remarkable rhythmical movements. The frustule
consists of a number of very fine short threads attached together by a
gelatinous sheath, in one species all of equal length. Their backward and
forward movement is of a most singular character; the only other conferva
in which I have seen a motion of a similar kind is the Schizonema. In this
species the frustules are packed together in regular series, the front and side
views being always in the same direction. These several bodies move along
within the filamentous sheath without leaving their respective places. On
carefully following the movement, it is seen at first much extended, and
then more compressed, while the frustules become more linear in their
arrangement, and present a closer resemblance to Bacillaria paradoxa,
augmented by the circumstance that the frustules are seen to move in both
directions. A frustule of Schizonema can move independently of the sheath,
and so will a detached frustule of bacillaria. This peculiar and exceptionally
anomalous phenomenon as that of the movements of bacillaria can hardly
be confined to a solitary species. The movements of the frustules are much
accelerated by warmth and light. The longer filaments of other minute
species only slightly exhibit any motion of the kind, but have peculiar
undulating motions.
Confervaceæ are a genus of algals. The species consist of unbranched
filaments composed of cylindrical or moniliform cells, with starch granules.
Many are vesicular, and all multiply by zoospores generated in the interior
of the plant at the expense of the granular matter. They are, for the most
part, found in fresh water attached or floating, some in salt water, and a few
in both, in colour usually green, but occasionally olive, violet, and red. The
Confervaceæ proper are often divided into four families: 1. Hydrodictidæ;
2. Zygnemidæ; 3. Confervidæ; 4. Chætophoridæ. To the microscopist all the
Page 477
plants of this genera are
extremely interesting as subjects
for the study of cell
multiplication. The process
usually takes place in the
terminal cell, the first step in
which is the division of the
endochrome, and then follows a
sort of hour-glass contraction
across the cavity of the parent
cell, whereby it is divided into
two equal parts. This is better
seen in some of the desmids than
in Fig. 284, Nos. 4, 5, and 6.
Some species are characterised
by a different mode of
reproduction; these possess a
number of nuclei, and multiply
Fig. 284.—Confervaceæ. by zoospores of two kinds, the
1. Volvox globator; 2. A section of volvox, largest of which have either two
showing the flagellate margin of the cell; 3. A or four cilia, which germinate
portion more highly magnified, to show the directly the smaller are
young volvocina, with their nuclei and thread-
like attachments; 4. Spirogyra, near which are biciliated; conjugation has been
spores in different stages of development; 5. seen to take place in a few
Conferva floccosa; 6. Stigeoclonium protensum,
jointed filaments and single zoospores; 7.
instances.
Staurocarpus gracilis, conjugating filaments and
spores. Allied to the Confervaceæ is an
interesting plant, Sphæroplea
annulina, which has received careful attention from Cohn. The oospores of
this plant are the product of a process partaking of a sexual nature, and
when mature are filled with reddish fat vesicles which divide by
segmentation.
The Ædogoniaceæ also closely resemble Confervaceæ in habits of life, but
differ in some particulars, especially so in the mode of reproduction (only a
single large zoospore being set free from each cell) and by the almost
complete fission of the cell-wall or one of the rings which serve as a hinge.
extremely interesting as subjects
for the study of cell
multiplication. The process
usually takes place in the
terminal cell, the first step in
which is the division of the
endochrome, and then follows a
sort of hour-glass contraction
across the cavity of the parent
cell, whereby it is divided into
two equal parts. This is better
seen in some of the desmids than
in Fig. 284, Nos. 4, 5, and 6.
Some species are characterised
by a different mode of
reproduction; these possess a
number of nuclei, and multiply
Fig. 284.—Confervaceæ. by zoospores of two kinds, the
1. Volvox globator; 2. A section of volvox, largest of which have either two
showing the flagellate margin of the cell; 3. A or four cilia, which germinate
portion more highly magnified, to show the directly the smaller are
young volvocina, with their nuclei and thread-
like attachments; 4. Spirogyra, near which are biciliated; conjugation has been
spores in different stages of development; 5. seen to take place in a few
Conferva floccosa; 6. Stigeoclonium protensum,
jointed filaments and single zoospores; 7.
instances.
Staurocarpus gracilis, conjugating filaments and
spores. Allied to the Confervaceæ is an
interesting plant, Sphæroplea
annulina, which has received careful attention from Cohn. The oospores of
this plant are the product of a process partaking of a sexual nature, and
when mature are filled with reddish fat vesicles which divide by
segmentation.
The Ædogoniaceæ also closely resemble Confervaceæ in habits of life, but
differ in some particulars, especially so in the mode of reproduction (only a
single large zoospore being set free from each cell) and by the almost
complete fission of the cell-wall or one of the rings which serve as a hinge.
Page 478
The zoospores are the largest known among algals, and each is described as
having a red eye-spot. The Chætophoraceæ form an interesting group of
confervoid plants, and are usually found in running streams, as they prefer
pure water. One of the characteristics of the group is that the extremities of
the branches are prolonged into an acute-shaped termination, as represented
in Fig. 284, No. 6. A very pretty object under the microscope is
Draparnaldia glomerata, belonging to this species. It consists of an axis
composed of a row of cells, and at regular intervals whorls of slender
prolongations, containing chlorophyll or endochrome of a deeper green;
these attain to an extraordinary length.
The Batrachospermæ bear a strong resemblance to frog-spawn, from which
they derive their name, and are chiefly a marine group of algals allied to the
Rhodespermeæ or red seaweeds. The late Dr. A. Hassall first described
them; they have since received more careful attention from M. Sirodot.
They are reddish-green, extremely flexible, and nothing can surpass the
grace of their movements in water; but when removed from their element
they lose all form, and resemble a jelly-like substance without a trace of
organisation; but if allowed to remain quiet they regain their original shape.
The presence of the cell-membrane will be best demonstrated by breaking
up the filaments, either by moving the thin glass cover, or by cutting
through a mass of them in all directions with a fine dissecting knife. On
now examining the slide, in most instances many detached empty pieces of
the cell-membrane, with its striæ, will be seen, as well as filaments partly
deprived of protoplasm. On the application of iodine all these appearances
become more distinguishable in consequence of the filament turning red or
brown, while the empty cells remain either unaffected, or present a slight
yellowish tint, as is frequently the case with cellulose when old.
With regard to the contents of the cell, the endochrome is coloured in the
Oscillatoriæ, and is distinguishable by circular bands or rings around the
axis of the cylindrical filament. Iodine stains them brown or red, and syrup
and dilute sulphuric acid produce a beautiful rose colour. As to their mode
of propagation, nothing positive is known. If kept for some time they
gradually lose their green colour; a portion of the mass, becoming brown,
sinks to the bottom of the vessel, and presents a granular layer.
having a red eye-spot. The Chætophoraceæ form an interesting group of
confervoid plants, and are usually found in running streams, as they prefer
pure water. One of the characteristics of the group is that the extremities of
the branches are prolonged into an acute-shaped termination, as represented
in Fig. 284, No. 6. A very pretty object under the microscope is
Draparnaldia glomerata, belonging to this species. It consists of an axis
composed of a row of cells, and at regular intervals whorls of slender
prolongations, containing chlorophyll or endochrome of a deeper green;
these attain to an extraordinary length.
The Batrachospermæ bear a strong resemblance to frog-spawn, from which
they derive their name, and are chiefly a marine group of algals allied to the
Rhodespermeæ or red seaweeds. The late Dr. A. Hassall first described
them; they have since received more careful attention from M. Sirodot.
They are reddish-green, extremely flexible, and nothing can surpass the
grace of their movements in water; but when removed from their element
they lose all form, and resemble a jelly-like substance without a trace of
organisation; but if allowed to remain quiet they regain their original shape.
The presence of the cell-membrane will be best demonstrated by breaking
up the filaments, either by moving the thin glass cover, or by cutting
through a mass of them in all directions with a fine dissecting knife. On
now examining the slide, in most instances many detached empty pieces of
the cell-membrane, with its striæ, will be seen, as well as filaments partly
deprived of protoplasm. On the application of iodine all these appearances
become more distinguishable in consequence of the filament turning red or
brown, while the empty cells remain either unaffected, or present a slight
yellowish tint, as is frequently the case with cellulose when old.
With regard to the contents of the cell, the endochrome is coloured in the
Oscillatoriæ, and is distinguishable by circular bands or rings around the
axis of the cylindrical filament. Iodine stains them brown or red, and syrup
and dilute sulphuric acid produce a beautiful rose colour. As to their mode
of propagation, nothing positive is known. If kept for some time they
gradually lose their green colour; a portion of the mass, becoming brown,
sinks to the bottom of the vessel, and presents a granular layer.
Page 479
Mesoglia vermicularis (Fig. 285) consists
of strings of cells cohering and held
together by their membranous covering. In
the lowly organised plant Vaucheria (Plate
I., No. 23, V. sessilis)—so named after its
discoverer Vaucher, a German botanist—a
genus of Siphonaceæ, we have an example
of true processes of sexual generation. The
branching filaments are often seen to bear
at their sides peculiar globular bodies or
oval protuberances, nipple-shaped
buddings-out of the cell-wall, filled with a
dark-coloured endochrome and distributed
in pairs, one of which curves round to meet
the other, when conjugation is seen to take
place. Near these bodies others are found
Fig. 285.—Mesoglia vermicularis. with pointed projections, which have been
described as “horns,” but these, Pringshelm
says, are “antherids which produce antherozoids in their interior,” while the
capsule-like bodies constituting the oospores become, when fertilised, a
new generation, which swarm out through a cavity or aperture in the parent
cell-wall.
The fruit of fresh-water and most olive-green algals is enclosed in spherical
cavities under the epidermis of the frond, termed conceptacles, and may be
either male or female. The zoids are bottle-shaped and have flagella; the
transparent vesicle in which they are contained is itself enclosed in a second
of similar form. In monœcious and diœcious algals the female conceptacles
are distinguished from the male by their olive colour. The spores, when
developed, are borne on a pedicle emanating from the inner wall of the
conceptacle. They rupture the outer wall at its apex; at first the spore
appears simple, but soon after a series of changes takes place, consisting in
a splitting up of the endochrome into six or eight masses of spheroidal
bodies. A budding-out occurs in a few hours’ time, and ultimately elongates
into a cylindrical thread. The Vaucheria present a double mode of
reproduction, and their fronds consist of branching tubes resembling in their
general character that of the Bryophyta, from which indeed they differ only
of strings of cells cohering and held
together by their membranous covering. In
the lowly organised plant Vaucheria (Plate
I., No. 23, V. sessilis)—so named after its
discoverer Vaucher, a German botanist—a
genus of Siphonaceæ, we have an example
of true processes of sexual generation. The
branching filaments are often seen to bear
at their sides peculiar globular bodies or
oval protuberances, nipple-shaped
buddings-out of the cell-wall, filled with a
dark-coloured endochrome and distributed
in pairs, one of which curves round to meet
the other, when conjugation is seen to take
place. Near these bodies others are found
Fig. 285.—Mesoglia vermicularis. with pointed projections, which have been
described as “horns,” but these, Pringshelm
says, are “antherids which produce antherozoids in their interior,” while the
capsule-like bodies constituting the oospores become, when fertilised, a
new generation, which swarm out through a cavity or aperture in the parent
cell-wall.
The fruit of fresh-water and most olive-green algals is enclosed in spherical
cavities under the epidermis of the frond, termed conceptacles, and may be
either male or female. The zoids are bottle-shaped and have flagella; the
transparent vesicle in which they are contained is itself enclosed in a second
of similar form. In monœcious and diœcious algals the female conceptacles
are distinguished from the male by their olive colour. The spores, when
developed, are borne on a pedicle emanating from the inner wall of the
conceptacle. They rupture the outer wall at its apex; at first the spore
appears simple, but soon after a series of changes takes place, consisting in
a splitting up of the endochrome into six or eight masses of spheroidal
bodies. A budding-out occurs in a few hours’ time, and ultimately elongates
into a cylindrical thread. The Vaucheria present a double mode of
reproduction, and their fronds consist of branching tubes resembling in their
general character that of the Bryophyta, from which indeed they differ only
Page 480
in respect of the arrangement of their green contents. In that most
remarkable plant Saprolegnia ferox, which is structurally so closely allied to
Vaucheria, though separated from them by the absence of green colouring
matter, a corresponding analogy in the processes of development takes
place. In the formation of its zoospores, an intermediate step is presented
between that of the algæ and a class of plants formally placed among fungi.
The Ulvaceæ.—The typical form of seaweeds is the Ulva lactuca, well
known from its fronds of dark-green “laver” on every coast throughout the
world. Ulvæ are seen to differ but little from the preceding group of fresh-
water algals. The specific difference is that the cells, when multiplied by
binary subdivision, not only remain in firm connection with each other but
possess a more regular arrangement. The frond plane of the algal is either
more simple or lobed, and is formed of a double layer of cells closely
packed together and producing zoospores. The whole group is chiefly
distinguished from Porphyra by their green colour, the latter being roseate
or purple. Ulvæ are mostly marine, with one or two exceptions. One species
(U. thermalis) grows in the hot springs of Gastein, in a temperature of about
117° Fahr. The development of Ulvæ is seen in Fig. 286. The isolated cells,
A, resemble in some points those of the Protococcus; these give rise to
successive subdivisions determining the clusters seen at B and C, and by
their aggregation to the confervoid filament shown at D. These filaments
increase in length and breadth by successive additions, and finally take the
form of fronds, or rows of cells.
remarkable plant Saprolegnia ferox, which is structurally so closely allied to
Vaucheria, though separated from them by the absence of green colouring
matter, a corresponding analogy in the processes of development takes
place. In the formation of its zoospores, an intermediate step is presented
between that of the algæ and a class of plants formally placed among fungi.
The Ulvaceæ.—The typical form of seaweeds is the Ulva lactuca, well
known from its fronds of dark-green “laver” on every coast throughout the
world. Ulvæ are seen to differ but little from the preceding group of fresh-
water algals. The specific difference is that the cells, when multiplied by
binary subdivision, not only remain in firm connection with each other but
possess a more regular arrangement. The frond plane of the algal is either
more simple or lobed, and is formed of a double layer of cells closely
packed together and producing zoospores. The whole group is chiefly
distinguished from Porphyra by their green colour, the latter being roseate
or purple. Ulvæ are mostly marine, with one or two exceptions. One species
(U. thermalis) grows in the hot springs of Gastein, in a temperature of about
117° Fahr. The development of Ulvæ is seen in Fig. 286. The isolated cells,
A, resemble in some points those of the Protococcus; these give rise to
successive subdivisions determining the clusters seen at B and C, and by
their aggregation to the confervoid filament shown at D. These filaments
increase in length and breadth by successive additions, and finally take the
form of fronds, or rows of cells.
Page 481
Fig. 287.—Sphacelaria
Fig. 286.—Successive Stages of Development of Ulvæ. cirrhosa, with spores
A. Isolated spores; B and C. Clusters of cells; D. Cells in the borne at the sides of
filamentous stage. the branchlets.
The marine greenish-olive algæ present a general appearance which might
at first sight be mistaken for plants of a higher order of cryptogams. Their
fronds have no longer the form of a filament, but assume that of a
membranous expansion of cells. The cells in which zoospores are found
have an increased quantity of coloured protoplasm accumulated towards
one point of the cell-wall; while the zoospores are observed to converge
with their apices towards the same point. In some algæ, which seem to be
closely related in form and structure to the Bryophyta, we notice this
important difference, that the zoospores are developed in an organ specially
destined for the purpose, presenting peculiarities of form and distinguishing
it from other parts of the branching tubular frond. In the genus Derbesia
distinct spore cases develop, a young branch of which, when destined to
become a spore case, instead of elongating indefinitely, begins, after having
arrived at a certain length, to swell out into an ovoid vesicle, in the cavity of
which a considerable accumulation of protoplasm takes place. This is
separated from the rest of the plant, and becomes an opaque mass,
surrounded by a distinct membrane. After a time a division of the mass
Fig. 286.—Successive Stages of Development of Ulvæ. cirrhosa, with spores
A. Isolated spores; B and C. Clusters of cells; D. Cells in the borne at the sides of
filamentous stage. the branchlets.
The marine greenish-olive algæ present a general appearance which might
at first sight be mistaken for plants of a higher order of cryptogams. Their
fronds have no longer the form of a filament, but assume that of a
membranous expansion of cells. The cells in which zoospores are found
have an increased quantity of coloured protoplasm accumulated towards
one point of the cell-wall; while the zoospores are observed to converge
with their apices towards the same point. In some algæ, which seem to be
closely related in form and structure to the Bryophyta, we notice this
important difference, that the zoospores are developed in an organ specially
destined for the purpose, presenting peculiarities of form and distinguishing
it from other parts of the branching tubular frond. In the genus Derbesia
distinct spore cases develop, a young branch of which, when destined to
become a spore case, instead of elongating indefinitely, begins, after having
arrived at a certain length, to swell out into an ovoid vesicle, in the cavity of
which a considerable accumulation of protoplasm takes place. This is
separated from the rest of the plant, and becomes an opaque mass,
surrounded by a distinct membrane. After a time a division of the mass
Page 482
takes place, and a number of pyriform zoospores, each of which is
furnished with flagella, are set free.
Desmidiaceæ, Diatomaceæ, Algæ.
Tuffen West, del. Edmund Evans.
Plate II.
In Cutleria (Fig. 288) we have a special feature of interest with two kinds of
organs, seemingly opposed to each other with regard to their reproductive
functions. The sporangia not only differ from those of other species, but the
frond consists of olive-coloured irregularly-divided flagella, on each side of
which tufts (sori) consisting of the reproductive organs, intermixed with
hair-like bodies, are scattered. The zoospores are divided by transverse
partitions into four cavities, each of which is again bisected by a
furnished with flagella, are set free.
Desmidiaceæ, Diatomaceæ, Algæ.
Tuffen West, del. Edmund Evans.
Plate II.
In Cutleria (Fig. 288) we have a special feature of interest with two kinds of
organs, seemingly opposed to each other with regard to their reproductive
functions. The sporangia not only differ from those of other species, but the
frond consists of olive-coloured irregularly-divided flagella, on each side of
which tufts (sori) consisting of the reproductive organs, intermixed with
hair-like bodies, are scattered. The zoospores are divided by transverse
partitions into four cavities, each of which is again bisected by a
Page 483
longitudinal median septum.
When first thrown off they are in
appearance so much like the
spores of Puccinia that they may
be mistaken for them, although
so very much larger than those of
other olive-coloured algæ.
Florideæ, the red algæ (Plate II.),
present many varieties of
structure, although less appears
to be known of their reproductive
processes than of lower forms of
cryptogamic plants. These are,
however, of three kinds. The
first, to which the term polyspore
has been applied, is that of a
gelatinous or membranous Fig. 288.—Cutleria dichotoma. Section of lacinia of a
frond, showing the stalked eight-chambered
pericarp or conceptacle, in which oosporanges growing on tufts with intercalated
an indefinite number of filaments. Magnified 50 diameters.
zoospores are contained. This
organ may be either at the summit or base of a branch, or it may be
concealed in or below the cortical layer of the stem. In some cases a number
of spore-bearing filaments emanate from a kind of membrane at the base of
a spheroidal cellular perisporangium, by the rupture of which the zoospores
formed from the endochrome of the filaments make their escape. Other
changes have been observed; however, they all agree in one particular,
namely, that the zoospore is developed in the interior of a cell, the wall of
which forms its perispore, and the internal protoplasmic membrane
endochrome, the zoospore itself, for the escape of which the perispore
opens out at its apex.
The second form is more simple, and consists of a globular or ovoid cell,
containing a central granular mass; this ultimately divides into four
quadrate-shaped spores; these, on attaining maturity, escape by rupture of
the cell-wall. Another organ, called a tetraspore, takes its origin in the
cortical layer. The tetraspores are arranged either in an isolated manner
When first thrown off they are in
appearance so much like the
spores of Puccinia that they may
be mistaken for them, although
so very much larger than those of
other olive-coloured algæ.
Florideæ, the red algæ (Plate II.),
present many varieties of
structure, although less appears
to be known of their reproductive
processes than of lower forms of
cryptogamic plants. These are,
however, of three kinds. The
first, to which the term polyspore
has been applied, is that of a
gelatinous or membranous Fig. 288.—Cutleria dichotoma. Section of lacinia of a
frond, showing the stalked eight-chambered
pericarp or conceptacle, in which oosporanges growing on tufts with intercalated
an indefinite number of filaments. Magnified 50 diameters.
zoospores are contained. This
organ may be either at the summit or base of a branch, or it may be
concealed in or below the cortical layer of the stem. In some cases a number
of spore-bearing filaments emanate from a kind of membrane at the base of
a spheroidal cellular perisporangium, by the rupture of which the zoospores
formed from the endochrome of the filaments make their escape. Other
changes have been observed; however, they all agree in one particular,
namely, that the zoospore is developed in the interior of a cell, the wall of
which forms its perispore, and the internal protoplasmic membrane
endochrome, the zoospore itself, for the escape of which the perispore
opens out at its apex.
The second form is more simple, and consists of a globular or ovoid cell,
containing a central granular mass; this ultimately divides into four
quadrate-shaped spores; these, on attaining maturity, escape by rupture of
the cell-wall. Another organ, called a tetraspore, takes its origin in the
cortical layer. The tetraspores are arranged either in an isolated manner
Page 484
along the branches, or in
numbers together; in some
instances the branches that
contain them are so modified in
form they look like special
organs, and have been called
stichidia; as, for example, in
Dasya (Fig. 289). Of the third
kind of reproductive organ a
difference of opinion exists as to
the signification of their
antheridia; although always
produced in precisely the same
situations as the tetraspores and
polyspores, they are
agglomerations of little
colourless cells, either united in a
Fig. 289.—Dasya kutzingiana, with seed vessel and
two rows of tetraspores. Magnified 50 diameters. bunch, as in Griffithsia, or
enclosed in a transparent
cylinder, as in Polysiphonia, or covering a kind of expanded disc of peculiar
form, as in Laurencia. According to competent observers, the cells contain
spermatozoids. Nägeli describes the spermatozoid as a spiral fibre, which,
as it escapes, lengthens itself in the form of a screw. Thuret, on the contrary,
says the contents are granular, and offer no trace of a spiral filament, but are
expelled from the cells by a slow motion. The antheridia appear in their
most simple form in Callithamnion (Plate II., Nos. 32 and 34), being
reduced to a small mass of cells composed by numerous little bunches
which are sessile on the bifurcations of the terminal branches. The spores
are simpler structures than the tetraspores, and mostly occupy a more
important position. They are not scattered through the frond, but grouped in
definite masses, and generally enclosed in a special capsule or conceptacle,
which may be mistaken for a tetraspore case. The simplest form of the spore
fruit consists of spherical masses of spores attached to the wall of the frond,
or imbedded in its substance, without a proper conceptacle; such a fruit is
called a favellidium, and occurs in Halymenia; the same name is applied to
the fruits of similar structures not perfectly immersed, as those of Gigartina,
Gelidium, &c., where they form tubercular swellings on the lobes. In some,
numbers together; in some
instances the branches that
contain them are so modified in
form they look like special
organs, and have been called
stichidia; as, for example, in
Dasya (Fig. 289). Of the third
kind of reproductive organ a
difference of opinion exists as to
the signification of their
antheridia; although always
produced in precisely the same
situations as the tetraspores and
polyspores, they are
agglomerations of little
colourless cells, either united in a
Fig. 289.—Dasya kutzingiana, with seed vessel and
two rows of tetraspores. Magnified 50 diameters. bunch, as in Griffithsia, or
enclosed in a transparent
cylinder, as in Polysiphonia, or covering a kind of expanded disc of peculiar
form, as in Laurencia. According to competent observers, the cells contain
spermatozoids. Nägeli describes the spermatozoid as a spiral fibre, which,
as it escapes, lengthens itself in the form of a screw. Thuret, on the contrary,
says the contents are granular, and offer no trace of a spiral filament, but are
expelled from the cells by a slow motion. The antheridia appear in their
most simple form in Callithamnion (Plate II., Nos. 32 and 34), being
reduced to a small mass of cells composed by numerous little bunches
which are sessile on the bifurcations of the terminal branches. The spores
are simpler structures than the tetraspores, and mostly occupy a more
important position. They are not scattered through the frond, but grouped in
definite masses, and generally enclosed in a special capsule or conceptacle,
which may be mistaken for a tetraspore case. The simplest form of the spore
fruit consists of spherical masses of spores attached to the wall of the frond,
or imbedded in its substance, without a proper conceptacle; such a fruit is
called a favellidium, and occurs in Halymenia; the same name is applied to
the fruits of similar structures not perfectly immersed, as those of Gigartina,
Gelidium, &c., where they form tubercular swellings on the lobes. In some,
Page 485
the tubercles present a pore at the summit, through which the spores emerge
forth. In other cases, as in Ceramium (Plate II., Nos. 27 and 37), the spores
occupy a more conspicuous place; a characteristic species is Delessaria
(Plate II., No. 39), the coccidium either occurring on lateral branches, or is
sessile on the face of the frond, when it consists of a case filled with
angular-shaped spores attached to the wall of the case. The general external
appearance of the red algæ is very varied, but it seems to attain to its
deepest colouring in the Red Sea, which, it is said, is entirely due to the
peculiarly vivid red seaweed. They are all exquisite objects for the
microscope, as may be surmised from the few varieties presented in Plate
II. The Florideæ of the warmer seas exhibit most elegantly formed fronds,
as will be seen on reference to the “Phycologia Australica” of the late Dr.
William Harvey, F.R.S.
The Characeæ may be placed among the highest of the algals, if only for the
complexity of their reproductive organs, which certainly offer a contrast in
their simplicity of structure. Chara vulgaris, stonewort, is a simple fresh-
water plant, preferring still freshwater ponds or slow-moving rivers running
over a chalky soil. It thus derives the calcareous matter found in the axis of
the plant, together with a small portion of silica. Its filaments (or branches,
as some botanists prefer to call them) are given off in whorls. The Characeæ
are a small family of acrogens, consisting of only two or three at most. They
are monœcious and diœcious, the two kinds of fruit being often placed close
together. They may easily be grown in a tall glass jar for observation. All
that is necessary is to put the jar occasionally under the house tap and let the
water run slowly over the top for a short time, thus renewing the contents
without disturbing the plant. The hard water supplied to London suits chara
better than softer water. Both chara and nitella are objects of great interest
to microscopists, since in the former the important fact of vegetable
circulation was first observed. A portion of the plant of the natural size is
shown in Fig. 290, No. 1.
Characeæ.
forth. In other cases, as in Ceramium (Plate II., Nos. 27 and 37), the spores
occupy a more conspicuous place; a characteristic species is Delessaria
(Plate II., No. 39), the coccidium either occurring on lateral branches, or is
sessile on the face of the frond, when it consists of a case filled with
angular-shaped spores attached to the wall of the case. The general external
appearance of the red algæ is very varied, but it seems to attain to its
deepest colouring in the Red Sea, which, it is said, is entirely due to the
peculiarly vivid red seaweed. They are all exquisite objects for the
microscope, as may be surmised from the few varieties presented in Plate
II. The Florideæ of the warmer seas exhibit most elegantly formed fronds,
as will be seen on reference to the “Phycologia Australica” of the late Dr.
William Harvey, F.R.S.
The Characeæ may be placed among the highest of the algals, if only for the
complexity of their reproductive organs, which certainly offer a contrast in
their simplicity of structure. Chara vulgaris, stonewort, is a simple fresh-
water plant, preferring still freshwater ponds or slow-moving rivers running
over a chalky soil. It thus derives the calcareous matter found in the axis of
the plant, together with a small portion of silica. Its filaments (or branches,
as some botanists prefer to call them) are given off in whorls. The Characeæ
are a small family of acrogens, consisting of only two or three at most. They
are monœcious and diœcious, the two kinds of fruit being often placed close
together. They may easily be grown in a tall glass jar for observation. All
that is necessary is to put the jar occasionally under the house tap and let the
water run slowly over the top for a short time, thus renewing the contents
without disturbing the plant. The hard water supplied to London suits chara
better than softer water. Both chara and nitella are objects of great interest
to microscopists, since in the former the important fact of vegetable
circulation was first observed. A portion of the plant of the natural size is
shown in Fig. 290, No. 1.
Characeæ.
Page 486
Fig. 290.—Diagrammatic sketch of Chara.
1. A stem of Chara vulgaris, natural size; 2. Magnified view (arrows indicating the
course taken by the chlorophyll); 3. A limb, with buds protruding; 4. Portion of a
leaf of Vallisneria spiralis, showing cyclosis of chlorophyll granules.
Each plant is composed of an assemblage of long tubiform cells placed end
to end, with fixed intervals, around which the branchlets are disposed with
great regularity. In nitella the stem and branches are composed of simple
cells, which sometimes attain to several inches in length. Each node, or
zone, from which the branches spring, consists of a single plate, or layer, of
small cells, which are a continuation of the cortical layer of the internode
(Fig. 290, No. 3) as an outgrowth. Each cell is partially filled with
chlorophyll granules, and it is these that are seen under the microscope
taking the course shown by the arrows (Fig. 290, No. 2). The rate of
movement of the granules is accelerated by moderate warmth and retarded
1. A stem of Chara vulgaris, natural size; 2. Magnified view (arrows indicating the
course taken by the chlorophyll); 3. A limb, with buds protruding; 4. Portion of a
leaf of Vallisneria spiralis, showing cyclosis of chlorophyll granules.
Each plant is composed of an assemblage of long tubiform cells placed end
to end, with fixed intervals, around which the branchlets are disposed with
great regularity. In nitella the stem and branches are composed of simple
cells, which sometimes attain to several inches in length. Each node, or
zone, from which the branches spring, consists of a single plate, or layer, of
small cells, which are a continuation of the cortical layer of the internode
(Fig. 290, No. 3) as an outgrowth. Each cell is partially filled with
chlorophyll granules, and it is these that are seen under the microscope
taking the course shown by the arrows (Fig. 290, No. 2). The rate of
movement of the granules is accelerated by moderate warmth and retarded
Page 487
by cold. It is in viewing the circulation in water plants that the warm stage
of the microscope is brought into use. Borne along with the protoplasmic
stream are a number of solid particles consisting of starch granules and
other matters. The method of viewing the circulation is by cutting sections
off a portion of the plant with a very sharp knife, and arranging them in a
growing cell with a few drops of water, and covering over with a thin cover-
glass.
Fig. 291.—The Fructification of Chara fragilis.
A. Portion of filament containing “antheroids”; B. A group of antheridial filaments,
composed of a series of cells, within each of which antherozoids are formed; C.
The escape of mature antherozoids, with whip-like prolongations, about to swim
off; D. Antherid supported on flask-shaped pedicle; E. Nucule enlarging, and seen
to contain oospores; F. Spores and elaters of Equisetum; G. Spores surrounded by
elaters of Equisetum.
The reproductive process of Chara is effected by two sets of bodies, both of
which are placed at the base of the branches (Fig. 291, E and D) either on
the same or different plants, one set known as globules or antherids, and the
other as nucules, containing the oospores or archegones. These are often of
a bright red colour, and have covering plates, or shields (B and E), curiously
of the microscope is brought into use. Borne along with the protoplasmic
stream are a number of solid particles consisting of starch granules and
other matters. The method of viewing the circulation is by cutting sections
off a portion of the plant with a very sharp knife, and arranging them in a
growing cell with a few drops of water, and covering over with a thin cover-
glass.
Fig. 291.—The Fructification of Chara fragilis.
A. Portion of filament containing “antheroids”; B. A group of antheridial filaments,
composed of a series of cells, within each of which antherozoids are formed; C.
The escape of mature antherozoids, with whip-like prolongations, about to swim
off; D. Antherid supported on flask-shaped pedicle; E. Nucule enlarging, and seen
to contain oospores; F. Spores and elaters of Equisetum; G. Spores surrounded by
elaters of Equisetum.
The reproductive process of Chara is effected by two sets of bodies, both of
which are placed at the base of the branches (Fig. 291, E and D) either on
the same or different plants, one set known as globules or antherids, and the
other as nucules, containing the oospores or archegones. These are often of
a bright red colour, and have covering plates, or shields (B and E), curiously
Page 488
marked, and the central portion is composed of a number of filaments rolled
up (as in E) or free (as seen at B), projecting out from the centre of the
sphere. The antherid is supported on a short flask-shaped pedicle, which
projects into the interior. At the apex of each of the eight manubria is a
roundish hyaline cell, termed a capitulum, and at its apex again six smaller
or secondary capitula. The long whip-shaped filaments are divided by
transverse septa into a hundred or more compartments, every one of which
is filled with an antherozoid (as at A), consisting of a spiral thread of
protoplasm packed into two or three coils; these escape and become free (as
seen at C), each having two long fine flagella. The young antherozoid swims
off with a lashing action, and the whole field appears for a time filled with
life. They swim about freely, but their motion gradually ceases, and soon
they arrive at a state of inaction.
Nitella appears to have a somewhat different mode of fructification to that
of its congener. It puts forth a long filamentous branch from one of its
joints, which, on reaching the surface of the water, terminates in a whitish
fruit-like cluster. It is even a more delicate and less robust algal than chara,
and every care should be taken to imitate the still water in which it grows. It
delights in shady woods and in calcareous open pools.
Similar care is requisite with regard to Vallisneria; and a more equal
temperature is better suited to the growth of this aquatic plant. It should be
planted in the middle of the jar or aquarium, about two inches deep in
mould, closely pressed down, then gently fill the jar with water. When the
water requires changing, a small portion only should be run off at a time. It
appears to thrive in proportion to the frequency of changing the water, and
taking care that the water added rather increases the temperature than
lowers it.
The natural habitat of the Frog-bit, another water-plant of much interest, is
found on the surface of ponds and ditches; in the autumn its seeds fall, and
become buried in the mud at the bottom during the winter; in the spring
these plants rise to the surface, produce flowers, and grow throughout the
summer. Chara may be found in many places around London, and in the
upper reaches of the Thames.
up (as in E) or free (as seen at B), projecting out from the centre of the
sphere. The antherid is supported on a short flask-shaped pedicle, which
projects into the interior. At the apex of each of the eight manubria is a
roundish hyaline cell, termed a capitulum, and at its apex again six smaller
or secondary capitula. The long whip-shaped filaments are divided by
transverse septa into a hundred or more compartments, every one of which
is filled with an antherozoid (as at A), consisting of a spiral thread of
protoplasm packed into two or three coils; these escape and become free (as
seen at C), each having two long fine flagella. The young antherozoid swims
off with a lashing action, and the whole field appears for a time filled with
life. They swim about freely, but their motion gradually ceases, and soon
they arrive at a state of inaction.
Nitella appears to have a somewhat different mode of fructification to that
of its congener. It puts forth a long filamentous branch from one of its
joints, which, on reaching the surface of the water, terminates in a whitish
fruit-like cluster. It is even a more delicate and less robust algal than chara,
and every care should be taken to imitate the still water in which it grows. It
delights in shady woods and in calcareous open pools.
Similar care is requisite with regard to Vallisneria; and a more equal
temperature is better suited to the growth of this aquatic plant. It should be
planted in the middle of the jar or aquarium, about two inches deep in
mould, closely pressed down, then gently fill the jar with water. When the
water requires changing, a small portion only should be run off at a time. It
appears to thrive in proportion to the frequency of changing the water, and
taking care that the water added rather increases the temperature than
lowers it.
The natural habitat of the Frog-bit, another water-plant of much interest, is
found on the surface of ponds and ditches; in the autumn its seeds fall, and
become buried in the mud at the bottom during the winter; in the spring
these plants rise to the surface, produce flowers, and grow throughout the
summer. Chara may be found in many places around London, and in the
upper reaches of the Thames.
Page 489
Anacharis alsinastrum.—This remarkable plant is so unlike any other
water-plant that it may be at once recognised by its leaves growing in threes
round a slender stem. It is also known as “Waterthyme,” from a
resemblance it bears to that plant.
The colour of the plant is deep green; the leaves are nearly half an inch
long, by an eighth wide, egg-shaped at the point, with serrated edges. Its
powers of increase are prodigious, as every fragment is capable of
becoming an independent plant, producing roots and stems, and extending
itself indefinitely in every direction. The specific gravity of it is so nearly
that of water, that it is more disposed to sink than float. A small branch of
the plant is represented, with a hydra attached to it, in a subsequent chapter.
The special cells in which the circulation is most readily seen are the
elongated cells around the margin of the leaf and those of the midrib. On
examining the leaf with polarised light, the cells are observed to contain a
large proportion of silica, and present a very interesting appearance. A
bright band of light encircles the leaf, and traverses its centre. In fact, the
leaf is set, as it were, in a framework of silica. By boiling the leaf for a short
time in equal parts of nitric acid and water, a portion of the vegetable tissue
is destroyed, and the silica rendered more distinct, without changing the
form of the leaf.
It is necessary to make a thin section or strip from the leaf of Vallisneria for
the purpose of exhibiting the circulation in the cells, as shown in Fig. 290,
No. 4. Among the cell granules, a few of a more transparent character than
the rest, are seen to have a nucleolus within.
The phenomenon of cell cyclosis occurs in other plants beside those
growing in water. The leaf of the common plantain or dock, Plantago,
furnishes a good example, the movement being seen both in the cells of the
plant and hairs of the cuticle torn from the midrib.
Cell-division.—In order to study the process of cell-division the hairs on the
stamens of Tradescantia should be taken. Remove one from a bud on a
warm day and let a drop of a one per cent. sugar solution fall upon it, and
cover it with a thin glass cover. Place it for a short time in a moist-chamber
(Fig. 256), and then examine it with a magnifying power of 500 diameters.
water-plant that it may be at once recognised by its leaves growing in threes
round a slender stem. It is also known as “Waterthyme,” from a
resemblance it bears to that plant.
The colour of the plant is deep green; the leaves are nearly half an inch
long, by an eighth wide, egg-shaped at the point, with serrated edges. Its
powers of increase are prodigious, as every fragment is capable of
becoming an independent plant, producing roots and stems, and extending
itself indefinitely in every direction. The specific gravity of it is so nearly
that of water, that it is more disposed to sink than float. A small branch of
the plant is represented, with a hydra attached to it, in a subsequent chapter.
The special cells in which the circulation is most readily seen are the
elongated cells around the margin of the leaf and those of the midrib. On
examining the leaf with polarised light, the cells are observed to contain a
large proportion of silica, and present a very interesting appearance. A
bright band of light encircles the leaf, and traverses its centre. In fact, the
leaf is set, as it were, in a framework of silica. By boiling the leaf for a short
time in equal parts of nitric acid and water, a portion of the vegetable tissue
is destroyed, and the silica rendered more distinct, without changing the
form of the leaf.
It is necessary to make a thin section or strip from the leaf of Vallisneria for
the purpose of exhibiting the circulation in the cells, as shown in Fig. 290,
No. 4. Among the cell granules, a few of a more transparent character than
the rest, are seen to have a nucleolus within.
The phenomenon of cell cyclosis occurs in other plants beside those
growing in water. The leaf of the common plantain or dock, Plantago,
furnishes a good example, the movement being seen both in the cells of the
plant and hairs of the cuticle torn from the midrib.
Cell-division.—In order to study the process of cell-division the hairs on the
stamens of Tradescantia should be taken. Remove one from a bud on a
warm day and let a drop of a one per cent. sugar solution fall upon it, and
cover it with a thin glass cover. Place it for a short time in a moist-chamber
(Fig. 256), and then examine it with a magnifying power of 500 diameters.
Page 490
The nucleus of the cell will be seen, near its terminal position, to gradually
elongate in the direction of the longer axis of the cell and become more
granular, while the protoplasm moves towards the extreme end; the nucleus
at the same time will present a striated appearance, with the fibrilla
arranged parallel to the longer axis of the nucleus, and at length approach
each other at the poles. A nuclear spindle will now be produced, and the
fibres ruptured in the equatorial plane, so that two nuclei will be found in
place of the one. The best preparations of nuclei are obtained by making
thin longitudinal sections of actively-growing plants (young rootlets of
Pinus, for example), and staining them with hæmatoxylin in the manner
described in a former chapter.
Desmidiaceæ and Diatomaceæ.
The two groups of Desmidiaceæ and Diatomaceæ differ so little in their
general characters that they may be spoken of as members or representative
families of microscopic and unicellular algæ alike in their remarkable
beauty and bilateral symmetry, and of such peculiar interest as to call for
special notice. Desmids differ from diatoms chiefly in colour, in lacking a
non-silicious skeleton, and in their generative process, which for the most
part consists in the conjugation of two similar cells. Diatoms, on the other
hand, have dense silicious skeletons and a general absence of green
colouring matter. Ralfs, in his systematic monograph, enumerates twenty
genera of desmids. The limiting membrane is alike firm and flexible, since
it exhibits some elasticity and resistance to pressure, and is not readily
decomposable. Traces of silica are found in only a few of the desmids,
while the frustule of the diatom is chiefly composed of this substance; both
have an external membranous covering, so transparent and homogeneous in
structure as to be in danger of being entirely overlooked, unless some
staining material is used, together with a high-power objective possessing
considerable penetration. In some species, however, the mucous covering is
more clearly defined, as in Staurastrum and Didymoprium Grevelli.
Openings occur in the outer membrane of other species, as the Closterium.
PLATE X.
elongate in the direction of the longer axis of the cell and become more
granular, while the protoplasm moves towards the extreme end; the nucleus
at the same time will present a striated appearance, with the fibrilla
arranged parallel to the longer axis of the nucleus, and at length approach
each other at the poles. A nuclear spindle will now be produced, and the
fibres ruptured in the equatorial plane, so that two nuclei will be found in
place of the one. The best preparations of nuclei are obtained by making
thin longitudinal sections of actively-growing plants (young rootlets of
Pinus, for example), and staining them with hæmatoxylin in the manner
described in a former chapter.
Desmidiaceæ and Diatomaceæ.
The two groups of Desmidiaceæ and Diatomaceæ differ so little in their
general characters that they may be spoken of as members or representative
families of microscopic and unicellular algæ alike in their remarkable
beauty and bilateral symmetry, and of such peculiar interest as to call for
special notice. Desmids differ from diatoms chiefly in colour, in lacking a
non-silicious skeleton, and in their generative process, which for the most
part consists in the conjugation of two similar cells. Diatoms, on the other
hand, have dense silicious skeletons and a general absence of green
colouring matter. Ralfs, in his systematic monograph, enumerates twenty
genera of desmids. The limiting membrane is alike firm and flexible, since
it exhibits some elasticity and resistance to pressure, and is not readily
decomposable. Traces of silica are found in only a few of the desmids,
while the frustule of the diatom is chiefly composed of this substance; both
have an external membranous covering, so transparent and homogeneous in
structure as to be in danger of being entirely overlooked, unless some
staining material is used, together with a high-power objective possessing
considerable penetration. In some species, however, the mucous covering is
more clearly defined, as in Staurastrum and Didymoprium Grevelli.
Openings occur in the outer membrane of other species, as the Closterium.
PLATE X.
Page 491
DESMIDIACEÆ.
Many species of desmids have a power of motion, the cause of which must
be due either to cilia or a flagellate organ. This, however, is denied by some
observers, who regard their movements as due to an exudation of the
mucilaginous contents of the cell, to exosmose, or diffusion, neither of
which hypotheses will at all help us to understand the gliding movements of
the Oscillariæ or the sharp jerky movement of the Schizonema. The
movements of desmids are especially exerted when in the act of dividing,
and by sunlight, towards which they are always observed to move. The
force with which some diatoms move about is very great, and this can only
be satisfactorily explained by admitting a specialised organ.
The appearance of the Desmidiaceæ (Plate X.) is much modified by their
eminences, depressions, and processes, as well as that of the surface, the
Many species of desmids have a power of motion, the cause of which must
be due either to cilia or a flagellate organ. This, however, is denied by some
observers, who regard their movements as due to an exudation of the
mucilaginous contents of the cell, to exosmose, or diffusion, neither of
which hypotheses will at all help us to understand the gliding movements of
the Oscillariæ or the sharp jerky movement of the Schizonema. The
movements of desmids are especially exerted when in the act of dividing,
and by sunlight, towards which they are always observed to move. The
force with which some diatoms move about is very great, and this can only
be satisfactorily explained by admitting a specialised organ.
The appearance of the Desmidiaceæ (Plate X.) is much modified by their
eminences, depressions, and processes, as well as that of the surface, the
Page 492
margin of the fronds, and the depth and width of the central constriction.
The surfaces may be dotted over irregularly, the dots themselves being
elevated or depressed points in their structural character. The margins of
some have a dentate appearance, as in Cosmarium. In the elongated forms,
such as Penium, the puncta are disposed in lines parallel to the length. In
several these lines are either elevations or furrows, it is not always easy to
say which; they are peculiar, however, to the elongated forms of
Closterium. When the lines are fine they produce a striation of the surface,
but in order to discover this the fronds should be viewed when empty and
by a fairly good power. The modification of surface in several genera seems
to be due, not to mere simple appendages, but to expansion of the limiting
membrance into thickened processes, and which may terminate in spines, as
in Xanthidium and Staurastrum (Plate X., Nos. 8-19 and 22). A general
distribution over the surface is characteristic of the former, but in Euastrum
the surfaces are very irregular, and therefore described as “swellings or
inflations.” Micrasterias has its margin deeply incised into lobes, which in
some have a radiating arrangement; when the lobes on the margin are small
they constitute crenations or dentations. The fronds of Euastrum binatum
are bicrenate on the sides, as are those of Desmidium and Hyalotheca and
other species. Another variety of margin exists, known as undulating or
wavy, while the general concavity or convexity of the margins furnish other
specific characteristics.
Pediastreæ (Plate X., Nos. 24-29).—The members of this family formerly
included the Micrasterias and Arthrodesmius of Ehrenberg. From their
arrangement of cells in determinate numbers and definite forms, it has been
thought by some observers that they should be removed from the desmids
to a special or sub-family. The points of difference consist in the firmness of
the outer covering, in the frequent interruptions on the margin of the cells,
and in the protrusion of “horns,” or rather a notch more or less deep. It is
true that the cells are not made up of two symmetrical halves, and that they
are in aggregation, which is not (except in the Scenedesmus, a genus that
distinctly connects this group with desmids) in linear series, but in the form
of discoidal fronds. They, however, divide into 8, 16, or 32 gonidia, and
these move about for some time before the formation of a new frond. It was
Nägeli who first instituted a sub-genus of Pediastrum, under the designation
of Anomopedium, the chief characteristic of which is the absence of bilobed
The surfaces may be dotted over irregularly, the dots themselves being
elevated or depressed points in their structural character. The margins of
some have a dentate appearance, as in Cosmarium. In the elongated forms,
such as Penium, the puncta are disposed in lines parallel to the length. In
several these lines are either elevations or furrows, it is not always easy to
say which; they are peculiar, however, to the elongated forms of
Closterium. When the lines are fine they produce a striation of the surface,
but in order to discover this the fronds should be viewed when empty and
by a fairly good power. The modification of surface in several genera seems
to be due, not to mere simple appendages, but to expansion of the limiting
membrance into thickened processes, and which may terminate in spines, as
in Xanthidium and Staurastrum (Plate X., Nos. 8-19 and 22). A general
distribution over the surface is characteristic of the former, but in Euastrum
the surfaces are very irregular, and therefore described as “swellings or
inflations.” Micrasterias has its margin deeply incised into lobes, which in
some have a radiating arrangement; when the lobes on the margin are small
they constitute crenations or dentations. The fronds of Euastrum binatum
are bicrenate on the sides, as are those of Desmidium and Hyalotheca and
other species. Another variety of margin exists, known as undulating or
wavy, while the general concavity or convexity of the margins furnish other
specific characteristics.
Pediastreæ (Plate X., Nos. 24-29).—The members of this family formerly
included the Micrasterias and Arthrodesmius of Ehrenberg. From their
arrangement of cells in determinate numbers and definite forms, it has been
thought by some observers that they should be removed from the desmids
to a special or sub-family. The points of difference consist in the firmness of
the outer covering, in the frequent interruptions on the margin of the cells,
and in the protrusion of “horns,” or rather a notch more or less deep. It is
true that the cells are not made up of two symmetrical halves, and that they
are in aggregation, which is not (except in the Scenedesmus, a genus that
distinctly connects this group with desmids) in linear series, but in the form
of discoidal fronds. They, however, divide into 8, 16, or 32 gonidia, and
these move about for some time before the formation of a new frond. It was
Nägeli who first instituted a sub-genus of Pediastrum, under the designation
of Anomopedium, the chief characteristic of which is the absence of bilobed
Page 493
peripheral cells. In Cœlastrum the cells are hexangular, the central ones
very regularly so; in Sorastrum they are wedge-shaped, or triangular, with
rounded-off angles. Viewed laterally the cells appear oblong. The cells of
Pediastrum are considerably compressed, so that when aggregated they
form a flattened tubular structure; in figure they are polygonal, frequently
hexagonal, a shape owing, in all probability, to mutual lateral pressure
during growth. There is a pervading uniformity in the contents of the cells
of the different genera, which consist of protoplasmic endochrome. At first
the colour is pale green, but it becomes deeper with full maturity, while the
decaying cells are seen to change to a deep reddish-yellow or brown. The
protoplasm is also clear and homogeneous, but in time granules appear,
enlarge, and multiply in number; moreover, each cell presents a single
bright green vesicle, around which are collected clear circular spaces or
globules, recalling those of Closterium, and varying in number from two to
six or more, their position not being regulated by the partition wall as in
Palmellæ, but by the centre of the entire frond. Oil globules are also
contained in the cells; their presence is indicated by the addition of a drop
of tincture of iodine. On one occasion Nägeli saw in Pediastrum boryanum
the endochrome disposed in a radiating manner, an arrangement which
often obtains in algals and in other vegetable cells with a central nucleus.
The cells of Pediastreæ are always united together in compound fronds, as
represented in Plate X., Nos. 24 and 29.56
The differences pointed out in no way constitute a claim to remove
Pediastreæ from among Desmidiaceæ, certainly not to rank as a distinct
species.
Reproduction of Desmidiaceæ.—A true reproductive act is presented by the
conjugation or coupling of two fronds, and by the resulting development of
a sporangium and subsequent interchange of the contents of the two cells.
At another time self-division is frequently seen to take place in all respects
as in the cells of other algæ. The proceeding is varied in some essential
particulars by the form of the fronds and by other circumstances; as in
fission of Euastrum, for instance (seen in Plate X., Nos. 1, 2, and 12), when
the narrow connecting bands between the two segments of the fronds are
rapidly pushed aside by growth and finally divide. Two modes of
conjugation of fronds are represented in Plate X., Nos. 25 and 33, in
very regularly so; in Sorastrum they are wedge-shaped, or triangular, with
rounded-off angles. Viewed laterally the cells appear oblong. The cells of
Pediastrum are considerably compressed, so that when aggregated they
form a flattened tubular structure; in figure they are polygonal, frequently
hexagonal, a shape owing, in all probability, to mutual lateral pressure
during growth. There is a pervading uniformity in the contents of the cells
of the different genera, which consist of protoplasmic endochrome. At first
the colour is pale green, but it becomes deeper with full maturity, while the
decaying cells are seen to change to a deep reddish-yellow or brown. The
protoplasm is also clear and homogeneous, but in time granules appear,
enlarge, and multiply in number; moreover, each cell presents a single
bright green vesicle, around which are collected clear circular spaces or
globules, recalling those of Closterium, and varying in number from two to
six or more, their position not being regulated by the partition wall as in
Palmellæ, but by the centre of the entire frond. Oil globules are also
contained in the cells; their presence is indicated by the addition of a drop
of tincture of iodine. On one occasion Nägeli saw in Pediastrum boryanum
the endochrome disposed in a radiating manner, an arrangement which
often obtains in algals and in other vegetable cells with a central nucleus.
The cells of Pediastreæ are always united together in compound fronds, as
represented in Plate X., Nos. 24 and 29.56
The differences pointed out in no way constitute a claim to remove
Pediastreæ from among Desmidiaceæ, certainly not to rank as a distinct
species.
Reproduction of Desmidiaceæ.—A true reproductive act is presented by the
conjugation or coupling of two fronds, and by the resulting development of
a sporangium and subsequent interchange of the contents of the two cells.
At another time self-division is frequently seen to take place in all respects
as in the cells of other algæ. The proceeding is varied in some essential
particulars by the form of the fronds and by other circumstances; as in
fission of Euastrum, for instance (seen in Plate X., Nos. 1, 2, and 12), when
the narrow connecting bands between the two segments of the fronds are
rapidly pushed aside by growth and finally divide. Two modes of
conjugation of fronds are represented in Plate X., Nos. 25 and 33, in
Page 494
Closterium and Penium. The act of conjugation admits of variations in
character, as shown in Staurastrum and Microsterias; the contents of both
fronds are discharged into a delicate intermediate sac; this gradually
thickens and produces spines (Plate X., Nos. 8 and 19). In Didymoprium
the separate joints unite by a narrow process pushed out from each other,
often of considerable length, through which the endochrome of one cell is
transferred to the other, and thus a sporangium is produced within one of
two cells, just as in the conjugatæ (No. 5). In Penium Jennereri the
conjugation takes a varied form; the fronds do not open and gape at the
suture, but couple by small but distinct cylindrical tubes (No. 27).
Among those enumerated, the compressed and deeply constricted cells of
Euastrum offer the more favourable opportunities for studying the manner
of their division; for although the frond is really a single cell, in all its
stages it appears like two, the segments being always distinct, from the
earliest stage. The segments, however, are separated by a connecting link,
which is subsequently converted into two somewhat round hyaline bodies.
These bodies gradually increase and acquire colour, and as they grow the
original segments are further divided, and at length become disconnected,
each taking a new segment to supply the place of that from which it is
separated. It is curious to trace the progressive development of the newer
portions, which at first are devoid of all colour; but as they become larger a
faint green tint is observed, which gradually darkens, and then assumes a
granular appearance. Soon the new segments attain their normal size, while
the covering in some species shows the presence of puncta. In Xanthidium,
Plate X., Nos. 9, 10, and Staurastrum, Nos. 15-18, the spines and processes
make their appearance last, beginning as mere tubercles, and then
lengthening until they attain their perfect form and size, armed with setæ;
but complete separation frequently occurs before growth is fully completed.
This singular process is repeated again and again, so that the older segments
are united successively, as it were, with many generations. When the cells
approach maturity, molecular movements may be at times noticed in their
contents, precisely similar to what Agardh and others aptly term
“swarming.” Meyen describes this granular matter as starch.57 Closterium,
early in the spring, when freshly secured and exposed to light, presents a
wonderful appearance, these bodies being kept continually in motion at
both ends of the frustule by the ciliary action within the cell, and the whole
character, as shown in Staurastrum and Microsterias; the contents of both
fronds are discharged into a delicate intermediate sac; this gradually
thickens and produces spines (Plate X., Nos. 8 and 19). In Didymoprium
the separate joints unite by a narrow process pushed out from each other,
often of considerable length, through which the endochrome of one cell is
transferred to the other, and thus a sporangium is produced within one of
two cells, just as in the conjugatæ (No. 5). In Penium Jennereri the
conjugation takes a varied form; the fronds do not open and gape at the
suture, but couple by small but distinct cylindrical tubes (No. 27).
Among those enumerated, the compressed and deeply constricted cells of
Euastrum offer the more favourable opportunities for studying the manner
of their division; for although the frond is really a single cell, in all its
stages it appears like two, the segments being always distinct, from the
earliest stage. The segments, however, are separated by a connecting link,
which is subsequently converted into two somewhat round hyaline bodies.
These bodies gradually increase and acquire colour, and as they grow the
original segments are further divided, and at length become disconnected,
each taking a new segment to supply the place of that from which it is
separated. It is curious to trace the progressive development of the newer
portions, which at first are devoid of all colour; but as they become larger a
faint green tint is observed, which gradually darkens, and then assumes a
granular appearance. Soon the new segments attain their normal size, while
the covering in some species shows the presence of puncta. In Xanthidium,
Plate X., Nos. 9, 10, and Staurastrum, Nos. 15-18, the spines and processes
make their appearance last, beginning as mere tubercles, and then
lengthening until they attain their perfect form and size, armed with setæ;
but complete separation frequently occurs before growth is fully completed.
This singular process is repeated again and again, so that the older segments
are united successively, as it were, with many generations. When the cells
approach maturity, molecular movements may be at times noticed in their
contents, precisely similar to what Agardh and others aptly term
“swarming.” Meyen describes this granular matter as starch.57 Closterium,
early in the spring, when freshly secured and exposed to light, presents a
wonderful appearance, these bodies being kept continually in motion at
both ends of the frustule by the ciliary action within the cell, and the whole
Page 495
frond is seen brilliantly glittering with active cilia. When a gleam of
stronger light is allowed for a moment to fall on the frond, the rapid
undulations of the cilia produce a series of most delicate prismatic
Newton’s rings. The action and distribution of the cilia, together with the
cyclosis of the granular bodies in the frond, are better seen by the aid of
Wenham’s parabola or a good condenser with a central stop. One of the
wide angular objectives shows the circulation around the marginal portions
of the whole frond. The stream is seen to be running up the more external
portion, internal to which is another stream following a contrary direction;
this action, confined to the space between the mass of endochrome and the
outer portion of the cell-wall, is seen to pass above or around the space in
which cyclosis of the spores is taking place.
During the summer of 1854, the late Rev. Lord Sidney Godolphin Osborne
and myself became much interested in the remarkable family of Closteria.
Fig. 292 is a highly magnified view of Closterium lunula which I drew by
the aid of the camera-lucida at the time. There could be no doubt about the
ciliary action within the frond: it was in every way similar to that of the
branchiæ of the muscle, the same wavy motion, which gradually became
slower as the death of the desmid drew near. This was brought about earlier
when the cell was not kept supplied with fresh water.
stronger light is allowed for a moment to fall on the frond, the rapid
undulations of the cilia produce a series of most delicate prismatic
Newton’s rings. The action and distribution of the cilia, together with the
cyclosis of the granular bodies in the frond, are better seen by the aid of
Wenham’s parabola or a good condenser with a central stop. One of the
wide angular objectives shows the circulation around the marginal portions
of the whole frond. The stream is seen to be running up the more external
portion, internal to which is another stream following a contrary direction;
this action, confined to the space between the mass of endochrome and the
outer portion of the cell-wall, is seen to pass above or around the space in
which cyclosis of the spores is taking place.
During the summer of 1854, the late Rev. Lord Sidney Godolphin Osborne
and myself became much interested in the remarkable family of Closteria.
Fig. 292 is a highly magnified view of Closterium lunula which I drew by
the aid of the camera-lucida at the time. There could be no doubt about the
ciliary action within the frond: it was in every way similar to that of the
branchiæ of the muscle, the same wavy motion, which gradually became
slower as the death of the desmid drew near. This was brought about earlier
when the cell was not kept supplied with fresh water.
Page 496
Fig. 292.—Closterium lunula.
In diagram A, line b points to a cluster of ovoid bodies; these are seen at
intervals throughout the endochrome within the investing membrane. These
bodies are attached to the membrane by small pedicles, and are occasionally
seen in motion about the spot, from which they eventually break away, and
are carried off, by the circulating fluid, to the chambers at the extremities of
the frond; there they join a crowd of similar bodies, in constant motion
within the chambers, when the specimen is quite fresh. That the action of
these free granules or spores is “Brownian,” as surmised by some writers, is
in my opinion entirely fallacious. It is doubtless in a measure due to the
current brought about by the ciliary motion of the more fluid contents of the
cell.
The circulation, when made out over the centre of the frond, for instance at
a, is in appearance of a wholly different nature from that seen at the edges.
In the latter the matter circulated is that of granules, passing each other in
distinct lines, but in opposite directions; in the circulation as seen at a, the
streams are broad, tortuous, of far greater body, and passing with much less
rapidity. To see the centre circulation, use a Gillett’s illuminator and a 1⁄8th
or a 1⁄10th immersion; work the fine adjustment so as to bring the centre of
the frond into focus, then almost lose it by raising the objective; after this,
with great care, work the milled head until the darker body of the
endochrome is clearly brought out.
At B is an enlarged sketch of one extremity of the frond. The arrows within
the chamber pointing to b denote the direction of a strong current of fluid,
which can be occasionally followed throughout. It is acted upon by cilia at
the edges of the chamber, the greater impetus appearing to come from the
centre of the endochrome. The fluid is here acting in positive jets, that is,
with an almost arterial action; and according to the strength with which it is
propelled at the time, the loose floating bodies are sent to a greater or less
distance from the end of the frustule; the fluid is thus impelled from a
centre, and kept in activity by the lateral cilia, that create a rapid current and
give a turning motion to the free bodies. The line—a, in this diagram,
denotes the outline of the membrane which encloses the endochrome; on
both sides cilia can be seen. The circulation exterior to it passes and
In diagram A, line b points to a cluster of ovoid bodies; these are seen at
intervals throughout the endochrome within the investing membrane. These
bodies are attached to the membrane by small pedicles, and are occasionally
seen in motion about the spot, from which they eventually break away, and
are carried off, by the circulating fluid, to the chambers at the extremities of
the frond; there they join a crowd of similar bodies, in constant motion
within the chambers, when the specimen is quite fresh. That the action of
these free granules or spores is “Brownian,” as surmised by some writers, is
in my opinion entirely fallacious. It is doubtless in a measure due to the
current brought about by the ciliary motion of the more fluid contents of the
cell.
The circulation, when made out over the centre of the frond, for instance at
a, is in appearance of a wholly different nature from that seen at the edges.
In the latter the matter circulated is that of granules, passing each other in
distinct lines, but in opposite directions; in the circulation as seen at a, the
streams are broad, tortuous, of far greater body, and passing with much less
rapidity. To see the centre circulation, use a Gillett’s illuminator and a 1⁄8th
or a 1⁄10th immersion; work the fine adjustment so as to bring the centre of
the frond into focus, then almost lose it by raising the objective; after this,
with great care, work the milled head until the darker body of the
endochrome is clearly brought out.
At B is an enlarged sketch of one extremity of the frond. The arrows within
the chamber pointing to b denote the direction of a strong current of fluid,
which can be occasionally followed throughout. It is acted upon by cilia at
the edges of the chamber, the greater impetus appearing to come from the
centre of the endochrome. The fluid is here acting in positive jets, that is,
with an almost arterial action; and according to the strength with which it is
propelled at the time, the loose floating bodies are sent to a greater or less
distance from the end of the frustule; the fluid is thus impelled from a
centre, and kept in activity by the lateral cilia, that create a rapid current and
give a turning motion to the free bodies. The line—a, in this diagram,
denotes the outline of the membrane which encloses the endochrome; on
both sides cilia can be seen. The circulation exterior to it passes and
Page 497
repasses in opposite directions, in three or four distinct courses; these, when
they arrive at—c, seem to encounter a stream making its way towards an
aperture at the apex of the chamber; then they appear to be driven back
again by a stronger force. Some, however, do occasionally enter the
chamber, but very rarely will one of the bodies escape into the outer current,
and should it do so, is carried about until it becomes adherent to the side
wall of the frond.
With regard to the propagation of the C. lunula, I have never seen anything
like conjugation; but I have repeatedly seen self-division (shown at D a a).
This act is chiefly the work of one half of the frond. Having watched for
some time, one half is seen to remain passive, while the other has a lateral
motion from side to side, as if moving on an axis at the point of juncture;
the motion increases, is more active, until at last with a jerk one segment
separates itself from the other, as seen at E. It will be noticed that each end
of the segment is perfectly closed before separation finally takes place;
there is, however, only one perfect chamber, that belonging to the extremity
of the original entire frond. The circulation continues for some time
previous to and after subdivision, in both fronds, and by almost
imperceptible degrees increases in volume. From the end of the
endochrome symptoms of elongation of the frond take place, the semi-lunar
form gradually changes, elongates, and is more defined, until it takes the
form and outline of the fully-formed frustule at the extremity. The obtuse
end—b of the other portion of frond is at the same time elongating and
contracting, and in a few hours from the division of the one segment from
the other the appearance of each half is that of a nearly perfect frustule, the
chamber at the new end is complete, the globular circulation exterior to it
becomes affected by the circulation from within the said chamber, and,
shortly afterwards, some of the free bodies descend, and become exposed to
the current already going on in the chamber. E is a diagram of one end of a
C. didymotocum, in which the same process was well marked, and
completed while it was under observation.
It will appear to most observers that if the continuation of the widely-spread
family of Desmidiaceæ was wholly dependent upon conjugation and
subdivision of their frustules, a process requiring several hours for its
completion, the whole species must have long ago disappeared. It may be
they arrive at—c, seem to encounter a stream making its way towards an
aperture at the apex of the chamber; then they appear to be driven back
again by a stronger force. Some, however, do occasionally enter the
chamber, but very rarely will one of the bodies escape into the outer current,
and should it do so, is carried about until it becomes adherent to the side
wall of the frond.
With regard to the propagation of the C. lunula, I have never seen anything
like conjugation; but I have repeatedly seen self-division (shown at D a a).
This act is chiefly the work of one half of the frond. Having watched for
some time, one half is seen to remain passive, while the other has a lateral
motion from side to side, as if moving on an axis at the point of juncture;
the motion increases, is more active, until at last with a jerk one segment
separates itself from the other, as seen at E. It will be noticed that each end
of the segment is perfectly closed before separation finally takes place;
there is, however, only one perfect chamber, that belonging to the extremity
of the original entire frond. The circulation continues for some time
previous to and after subdivision, in both fronds, and by almost
imperceptible degrees increases in volume. From the end of the
endochrome symptoms of elongation of the frond take place, the semi-lunar
form gradually changes, elongates, and is more defined, until it takes the
form and outline of the fully-formed frustule at the extremity. The obtuse
end—b of the other portion of frond is at the same time elongating and
contracting, and in a few hours from the division of the one segment from
the other the appearance of each half is that of a nearly perfect frustule, the
chamber at the new end is complete, the globular circulation exterior to it
becomes affected by the circulation from within the said chamber, and,
shortly afterwards, some of the free bodies descend, and become exposed to
the current already going on in the chamber. E is a diagram of one end of a
C. didymotocum, in which the same process was well marked, and
completed while it was under observation.
It will appear to most observers that if the continuation of the widely-spread
family of Desmidiaceæ was wholly dependent upon conjugation and
subdivision of their frustules, a process requiring several hours for its
completion, the whole species must have long ago disappeared. It may be
Page 498
presumed then that some other mode of reproduction must prevail. In the
fresh-water algæ the two more general methods of multiplication are clearly
governed by the conditions of the seasons; the resting-spores securing
continuity of life during the winter, the swarm-spores spreading the plant
profusely during the warmer portion of the year, when rapid growth is
possible. I therefore regard the actively swarming bodies seen in continuous
motion at the two extreme portions of the frustule of Closterium lunula as
being either oospores or zoospores, by means of which reproduction takes
place.
Diatomaceæ, commonly called brittleworts, Plate XI., are chiefly
composed of two symmetrical valves, narrow and wand-like, navicular,
miniature boat-shaped, hence their name Navicula (little ship). Hitherto
they have excited the deepest interest among microscopists because of their
wonderfully minute structure, and the difficulty involved in determining
their exact nature and formation. Each individual diatom has a silicious
skeleton, spoken of as a frustule, frond, or cell, having a rectangular or
prismatic form, which mostly obtains in the whole family, the angles of the
junction of the two united valves being, as a rule, acute, and enclosing a
yellowish-brown endochrome. Deeply-notched frustules, like those of the
Desmidiaceæ, do not occur, and the production of spines and tubercles so
common in that family is rare in the Diatomaceæ. Great variety of outline
prevails, so much so that no rule in this respect can be formulated.
The frustules, however, are usually composed of two equal and similar
halves, but exceptions to this are found in the Actinomtheæ, Cocconcidæ,
and one or two other families. The extremities of some species, e.g.,
Nitzshia and Pleurosigma, are extremely elongated, forming long, filiform,
tubular processes; in Biddulphia and Rizoselenia, short tubular processes
from their margins. Great variety of outline may prevail in a genus, so
considerable indeed that no accurate definition can be given, the
characteristics shading off through several species until the similarity to an
assumed typical form is much diminished, which may again be modified by
accidental circumstances that surround the development of the silicious
frustule. It must not be forgotten that the figure is greatly modified or
entirely changed by the position of the valves, whether seen in one position
or another, as already explained in connection with “Errors of
fresh-water algæ the two more general methods of multiplication are clearly
governed by the conditions of the seasons; the resting-spores securing
continuity of life during the winter, the swarm-spores spreading the plant
profusely during the warmer portion of the year, when rapid growth is
possible. I therefore regard the actively swarming bodies seen in continuous
motion at the two extreme portions of the frustule of Closterium lunula as
being either oospores or zoospores, by means of which reproduction takes
place.
Diatomaceæ, commonly called brittleworts, Plate XI., are chiefly
composed of two symmetrical valves, narrow and wand-like, navicular,
miniature boat-shaped, hence their name Navicula (little ship). Hitherto
they have excited the deepest interest among microscopists because of their
wonderfully minute structure, and the difficulty involved in determining
their exact nature and formation. Each individual diatom has a silicious
skeleton, spoken of as a frustule, frond, or cell, having a rectangular or
prismatic form, which mostly obtains in the whole family, the angles of the
junction of the two united valves being, as a rule, acute, and enclosing a
yellowish-brown endochrome. Deeply-notched frustules, like those of the
Desmidiaceæ, do not occur, and the production of spines and tubercles so
common in that family is rare in the Diatomaceæ. Great variety of outline
prevails, so much so that no rule in this respect can be formulated.
The frustules, however, are usually composed of two equal and similar
halves, but exceptions to this are found in the Actinomtheæ, Cocconcidæ,
and one or two other families. The extremities of some species, e.g.,
Nitzshia and Pleurosigma, are extremely elongated, forming long, filiform,
tubular processes; in Biddulphia and Rizoselenia, short tubular processes
from their margins. Great variety of outline may prevail in a genus, so
considerable indeed that no accurate definition can be given, the
characteristics shading off through several species until the similarity to an
assumed typical form is much diminished, which may again be modified by
accidental circumstances that surround the development of the silicious
frustule. It must not be forgotten that the figure is greatly modified or
entirely changed by the position of the valves, whether seen in one position
or another, as already explained in connection with “Errors of
Page 499
Interpretation.” Again, in the genera Navicula, Pinnularia (Plate II., Nos. 33,
38, and 40), and others, the frustules are in one aspect boat-shaped, but in
the other either oblong with truncated ends, or prismatic. In the genus
Triceratium (Plate XI., No. 10), the difference of figure is very remarkable
as the front or side view is examined.
The sudden change in appearance presented to the eye as the frustule is seen
to roll over is rather peculiar. As a rule, therefore, we must examine all
specimens in every aspect, to accomplish which very shallow cells should
be selected, say of 1⁄100th of an inch deep, and covered with glass 1⁄250th of an
inch thick. A good penetrating objective should be used, and careful
illumination obtained. The Diatomaceæ are perhaps more widely distributed
than any other class of infusorial life; they are found in fresh, salt, and
brackish water; many grow attached to other bodies by a stalk (Plate II., No.
33, Licmophora and Achnanthidium); while others, as Pleurosigma, No. 40,
swim about freely.
PLATE XI.
38, and 40), and others, the frustules are in one aspect boat-shaped, but in
the other either oblong with truncated ends, or prismatic. In the genus
Triceratium (Plate XI., No. 10), the difference of figure is very remarkable
as the front or side view is examined.
The sudden change in appearance presented to the eye as the frustule is seen
to roll over is rather peculiar. As a rule, therefore, we must examine all
specimens in every aspect, to accomplish which very shallow cells should
be selected, say of 1⁄100th of an inch deep, and covered with glass 1⁄250th of an
inch thick. A good penetrating objective should be used, and careful
illumination obtained. The Diatomaceæ are perhaps more widely distributed
than any other class of infusorial life; they are found in fresh, salt, and
brackish water; many grow attached to other bodies by a stalk (Plate II., No.
33, Licmophora and Achnanthidium); while others, as Pleurosigma, No. 40,
swim about freely.
PLATE XI.
Page 500
DIATOMACEÆ, RECENT AND FOSSIL.
There are a considerable number of Diatomaceæ which, when in the young
state, are enclosed in a muco-gelatinous sheath; while others are attached by
stipes or stalk to algæ. It would be vain, in a limited space, to attempt a
description of this numerous and extensive family. Nägeli and other
observers describe a “mucilaginous pellicle on the inner layer of the
valves,” while, as Menghine observes, “an organic membrane ought to exist
both inside and outside, for the silica could not become solid except by
crystallizing or depositing itself on some pre-existing substance.” The
surface of the frustules is generally very beautifully sculptured, and the
markings assume the appearance of dots (puncta), stripes (striæ), ribs
(costæ), pinnules (pinnæ), of furrows and fine lines; longitudinal,
transverse, and radiating bands; canals or canaliculi; and of cells or areolæ;
There are a considerable number of Diatomaceæ which, when in the young
state, are enclosed in a muco-gelatinous sheath; while others are attached by
stipes or stalk to algæ. It would be vain, in a limited space, to attempt a
description of this numerous and extensive family. Nägeli and other
observers describe a “mucilaginous pellicle on the inner layer of the
valves,” while, as Menghine observes, “an organic membrane ought to exist
both inside and outside, for the silica could not become solid except by
crystallizing or depositing itself on some pre-existing substance.” The
surface of the frustules is generally very beautifully sculptured, and the
markings assume the appearance of dots (puncta), stripes (striæ), ribs
(costæ), pinnules (pinnæ), of furrows and fine lines; longitudinal,
transverse, and radiating bands; canals or canaliculi; and of cells or areolæ;
Page 501
whilst all present striking varieties and modifications in their form,
character, and degree of development. Again, the fine lines or striæ of many
frustules are resolvable into rows of minute dots or perforations, as occur in
Pleurosigma angulatum, delineated in the accompanying microphotograph
(Fig. 294), taken for the author purposely to show the markings on this
especially selected test diatom.
Fig. 293.
1. Pleurosigma attenuatum; 2. Pleurosigma angulatum; 3. Pleurosigma Spencerii.
Magnified 450 diameters.
The nature of the markings on the diatom valves is one of considerable
interest, and attempts have been made to produce them artificially, but
without success.
character, and degree of development. Again, the fine lines or striæ of many
frustules are resolvable into rows of minute dots or perforations, as occur in
Pleurosigma angulatum, delineated in the accompanying microphotograph
(Fig. 294), taken for the author purposely to show the markings on this
especially selected test diatom.
Fig. 293.
1. Pleurosigma attenuatum; 2. Pleurosigma angulatum; 3. Pleurosigma Spencerii.
Magnified 450 diameters.
The nature of the markings on the diatom valves is one of considerable
interest, and attempts have been made to produce them artificially, but
without success.
Page 502
Fig. 294.—Pleurosigma angulatum, magnified 4500 diameters.
(From a microphotograph taken by Zeiss with the 2 mm. aprochromatic objective,
1·30 numerical aperture, and projection eye-piece, No. 4.)
Professor Max Schultze devoted a great amount of time to the investigation
of the subject, and has recorded in a voluminous paper58 the results of his
observations. He says, “Most of the species of the Diatomaceæ are
characterised by the presence on their outer surface of certain differences of
relief, referable either to elevations or to depressions disposed in rows. The
opinions of microscopists with respect to the nature of these markings are
still somewhat divided. Whilst in the larger forms, and those distinguished
by their coarser dots, the appearance is manifestly due to the existence of
thinner spots in the valve, we cannot so easily explain the cause of the
(From a microphotograph taken by Zeiss with the 2 mm. aprochromatic objective,
1·30 numerical aperture, and projection eye-piece, No. 4.)
Professor Max Schultze devoted a great amount of time to the investigation
of the subject, and has recorded in a voluminous paper58 the results of his
observations. He says, “Most of the species of the Diatomaceæ are
characterised by the presence on their outer surface of certain differences of
relief, referable either to elevations or to depressions disposed in rows. The
opinions of microscopists with respect to the nature of these markings are
still somewhat divided. Whilst in the larger forms, and those distinguished
by their coarser dots, the appearance is manifestly due to the existence of
thinner spots in the valve, we cannot so easily explain the cause of the
Page 503
striation or punctation in Pleurosigma angulatum and similar finely-marked
forms.”
Dr. R. Zeiss some time ago furnished me with a microphotograph of a
frustule magnified 4500 diameters that seemed to confirm Mr. T. F. Smith’s
view of the structure of these valves. Dr. Van Heurck has also made a study
of this diatom, and concludes that the valves consist of two membranes of
thin films, and of an intermediate layer, the outer being pierced with
openings. The outer membrane is, he believes, “so delicate that it is easily
destroyed by acid or by friction, and the several processes employed in
cleaning and preparing it for microscopical examination. When the
openings or apertures of the internal portion are arranged in alternate rows
they assume the hexagonal form; when in straight rows, the openings are
seen to be square or oblong.” A description hardly in accord with Fig. 294.
Movements of Diatoms.
The late Professor Smith, in his “Synopsis of Diatoms,” refers to their
movements in the following terms: “I am constrained to believe that the
movements observed in the Diatomaceæ are due to forces operating within
the frustule, and are probably connected with the endosmotic and exosmotic
action of the cells. The fluids which are concerned in these actions must
enter, and be emitted through the minute foramina at the extremities of the
silicious valves.” Schultze’s researches, which were made at a later date,
carried this debatable question somewhat further. He is of opinion “that a
sarcode (protoplasmic) substance envelops the external surface of the
diatoms, and its movements are due to this agent exclusively.” His
investigations were mainly confined to P. angulatum, and to the larger P.
attenuatum (Fig. 293, 1 and 2), as the transverse markings on the frustule
do not impede to so great an extent the observation of what is going on
within. The living specimen of P. angulatum under the microscope usually
has its broad side turned to view, with one long curved “raphe” uppermost,
and the other in contact with the glass cover (Fig. 293). Within the frustule
the yellow colouring matter, “endochrome,” fills the cavity more or less
completely. In the broader part of the frustule these bands of endochrome
describe one or two complicated windings. It is only possible in those
forms.”
Dr. R. Zeiss some time ago furnished me with a microphotograph of a
frustule magnified 4500 diameters that seemed to confirm Mr. T. F. Smith’s
view of the structure of these valves. Dr. Van Heurck has also made a study
of this diatom, and concludes that the valves consist of two membranes of
thin films, and of an intermediate layer, the outer being pierced with
openings. The outer membrane is, he believes, “so delicate that it is easily
destroyed by acid or by friction, and the several processes employed in
cleaning and preparing it for microscopical examination. When the
openings or apertures of the internal portion are arranged in alternate rows
they assume the hexagonal form; when in straight rows, the openings are
seen to be square or oblong.” A description hardly in accord with Fig. 294.
Movements of Diatoms.
The late Professor Smith, in his “Synopsis of Diatoms,” refers to their
movements in the following terms: “I am constrained to believe that the
movements observed in the Diatomaceæ are due to forces operating within
the frustule, and are probably connected with the endosmotic and exosmotic
action of the cells. The fluids which are concerned in these actions must
enter, and be emitted through the minute foramina at the extremities of the
silicious valves.” Schultze’s researches, which were made at a later date,
carried this debatable question somewhat further. He is of opinion “that a
sarcode (protoplasmic) substance envelops the external surface of the
diatoms, and its movements are due to this agent exclusively.” His
investigations were mainly confined to P. angulatum, and to the larger P.
attenuatum (Fig. 293, 1 and 2), as the transverse markings on the frustule
do not impede to so great an extent the observation of what is going on
within. The living specimen of P. angulatum under the microscope usually
has its broad side turned to view, with one long curved “raphe” uppermost,
and the other in contact with the glass cover (Fig. 293). Within the frustule
the yellow colouring matter, “endochrome,” fills the cavity more or less
completely. In the broader part of the frustule these bands of endochrome
describe one or two complicated windings. It is only possible in those
Page 504
specimens in which the bands are narrow to properly trace their foldings,
and determine their number. The next objects which strike the eye on
examining a freshly-gathered Pleurosigma are numerous highly refractive
oil-globules. These are not, however, all in the same place, and one globule
appears nearer the observer than the other; their relative position is best
seen when a view of the narrow side of the frustule can be obtained, so that
one raphe is to the left and the other to the right. The blue-black colour
which is assumed by these globules after treating with acid demonstrates
their oleaginous nature. The middle of the cavity of the frustule is occupied,
in the larger navicula, by two large oil-globules (seen in the diagrammatic
Fig. 295), and by a colourless finely granular mass, whose position in the
body is not so clearly seen in the flat view as in the side view. Besides the
central mass, the conical cavities at either end of the frustule are seen to
enclose granular substance, and two linear extensions from each of three
masses are developed, closely underlying the raphæ. In the side view,
therefore, they appear attached to the right and left edges of the interior of
the frustule. This colourless granular substance carries in its centre, near the
middle part of the diatom, an imperfectly developed nucleus which is not
very easy to see, but may be demonstrated by the application of an acid.
The colourless substance is protoplasm, and encloses numerous small
refractive particles; this, on adding a drop of a one per cent. solution of
osmic acid, is coloured blue-black, and proves to be fat. It is, however,
exceedingly difficult to determine the exact limitations of the protoplasm,
on account of the highly refractive character of the silicious skeleton, and
the obstruction to the light presented by the endochrome.
At a short distance the protoplasm reappears, contracted into a considerable
mass, within the terminal ends of the frustule. Schultze observed in this part
of the protoplasm a rapid molecular movement, “cyclosis,” such as occurs
in Closterium, and also a current of the granules of the protoplasm along the
raphe. “Pleurosigma angulatum ‘crawls,’ as do all diatoms possessing a
raphe, along this line of suture. To crawl along, it must have a fixed
support.” “There is obviously,” adds Schultze, “but one explanation; it is
clear that there must be a band of protoplasm lying along the raphe, which
causes the particles of colouring matter to adhere, and gives rise to a gliding
movement. For there is but one phenomenon which can be compared with
the gliding motion of foreign bodies on the Diatomaceæ, and that is, the
and determine their number. The next objects which strike the eye on
examining a freshly-gathered Pleurosigma are numerous highly refractive
oil-globules. These are not, however, all in the same place, and one globule
appears nearer the observer than the other; their relative position is best
seen when a view of the narrow side of the frustule can be obtained, so that
one raphe is to the left and the other to the right. The blue-black colour
which is assumed by these globules after treating with acid demonstrates
their oleaginous nature. The middle of the cavity of the frustule is occupied,
in the larger navicula, by two large oil-globules (seen in the diagrammatic
Fig. 295), and by a colourless finely granular mass, whose position in the
body is not so clearly seen in the flat view as in the side view. Besides the
central mass, the conical cavities at either end of the frustule are seen to
enclose granular substance, and two linear extensions from each of three
masses are developed, closely underlying the raphæ. In the side view,
therefore, they appear attached to the right and left edges of the interior of
the frustule. This colourless granular substance carries in its centre, near the
middle part of the diatom, an imperfectly developed nucleus which is not
very easy to see, but may be demonstrated by the application of an acid.
The colourless substance is protoplasm, and encloses numerous small
refractive particles; this, on adding a drop of a one per cent. solution of
osmic acid, is coloured blue-black, and proves to be fat. It is, however,
exceedingly difficult to determine the exact limitations of the protoplasm,
on account of the highly refractive character of the silicious skeleton, and
the obstruction to the light presented by the endochrome.
At a short distance the protoplasm reappears, contracted into a considerable
mass, within the terminal ends of the frustule. Schultze observed in this part
of the protoplasm a rapid molecular movement, “cyclosis,” such as occurs
in Closterium, and also a current of the granules of the protoplasm along the
raphe. “Pleurosigma angulatum ‘crawls,’ as do all diatoms possessing a
raphe, along this line of suture. To crawl along, it must have a fixed
support.” “There is obviously,” adds Schultze, “but one explanation; it is
clear that there must be a band of protoplasm lying along the raphe, which
causes the particles of colouring matter to adhere, and gives rise to a gliding
movement. For there is but one phenomenon which can be compared with
the gliding motion of foreign bodies on the Diatomaceæ, and that is, the
Page 505
clinging to and casting off of particles by the pseudopodia of the rhizopod,
as observed, for instance, on placing a living Gromia or Miliolina in still
water with finely-powdered carmine. The nature of the adhesion and of the
motion is in both cases the same. And since, with diatoms as unicellular
organisms, protoplasm forms a large part of the cell (in many cases two
distinctly moving protoplasms), this implies that the external movements
are referable to the movements of the protoplasm.” It is quite evident to
those who have studied the movements of diatoms that they are surrounded
by a sarcode structure of a more pellucid character than that of Amœba. Six
years before Schultze’s observations were published, I wrote in a third
edition of my book, page 307, “The act of progression favours the notion of
contractile tentacular filaments—pseudopodia—as the organs of
locomotion and prehension.”
Since my former observations on the movements of diatoms, I have given
much attention to two forms, P. angulatum and Pinnularia. The powers
used were Hartnack’s No. 8, and Gunlack’s 1⁄16-inch immersion; Gillett’s
condenser illumination, with lamp flame edge turned to mirror and bull’s-
eye lens; a perforated slide with a square of thin glass ·006 cemented to it,
and a cover-glass of ·005. So far as I could satisfy myself, no terminal
space, as in the Closteria, could be seen, otherwise the course of the
gemmules is as freely traced as in that form. They are more minute than the
Closterium lunula granules, more steadily or slowly seen to pass up and
down one half the frustule towards the extremity, one half of the current
seeming to turn round upon its axis and descending towards the other. The
granules were thickly scattered at the apex, but gradually became fewer, and
the ascending and descending current tapered away towards the central
nodule, which became more filled up or closed in.
as observed, for instance, on placing a living Gromia or Miliolina in still
water with finely-powdered carmine. The nature of the adhesion and of the
motion is in both cases the same. And since, with diatoms as unicellular
organisms, protoplasm forms a large part of the cell (in many cases two
distinctly moving protoplasms), this implies that the external movements
are referable to the movements of the protoplasm.” It is quite evident to
those who have studied the movements of diatoms that they are surrounded
by a sarcode structure of a more pellucid character than that of Amœba. Six
years before Schultze’s observations were published, I wrote in a third
edition of my book, page 307, “The act of progression favours the notion of
contractile tentacular filaments—pseudopodia—as the organs of
locomotion and prehension.”
Since my former observations on the movements of diatoms, I have given
much attention to two forms, P. angulatum and Pinnularia. The powers
used were Hartnack’s No. 8, and Gunlack’s 1⁄16-inch immersion; Gillett’s
condenser illumination, with lamp flame edge turned to mirror and bull’s-
eye lens; a perforated slide with a square of thin glass ·006 cemented to it,
and a cover-glass of ·005. So far as I could satisfy myself, no terminal
space, as in the Closteria, could be seen, otherwise the course of the
gemmules is as freely traced as in that form. They are more minute than the
Closterium lunula granules, more steadily or slowly seen to pass up and
down one half the frustule towards the extremity, one half of the current
seeming to turn round upon its axis and descending towards the other. The
granules were thickly scattered at the apex, but gradually became fewer, and
the ascending and descending current tapered away towards the central
nodule, which became more filled up or closed in.
Page 506
Fig. 295.—Outline sketches of Pinnulariæ, showing vesicles.
Fig. 296.—Gomphonema constrictum. (From a microphotograph.)
Fig. 296.—Gomphonema constrictum. (From a microphotograph.)
Page 507
This beautiful sight was not confined to one frustule, but was exhibited in
all that were in a healthy condition. I examined several, and watched them
for a long time. The phenomenon described depends much upon the healthy
condition of the frustule at the time; as the movements of the diatoms
became sluggish, the circulation gradually slackens and then ceases
altogether. I also saw a somewhat similar action in the more active
specimens of P. hippocampus and Navicula cuspidata, but the coarser
markings and thickness of the wall of these diatoms seemed to place greater
difficulties in the way of observation than the finer valves of the P.
angulatum. One thing I believe is certain, that the circulation described is
precisely similar to that seen in the Closteria, or, on a much larger scale, in
Chara and the leaf of the Anacharis, bearing in mind also that in the
Closterium the cell is divided by a transverse suture, and in P. angulatum by
a longitudinal one (Plate II., Nos. 38-40). About the same time some very
lively specimens of the Pinnulariæ were sent to me, and the movements of
these frustules were more closely observed. One or two of the more active
would attack a body relatively larger than itself, it would also force its way
into a mass of granular matter, and then recede from it with a jerky motion.
In more than one instance a cell of Palmoglæa was seized and carried away
by the Pinnularia, the former at the time being actively engaged in the
process of cell division. Other diatoms present among my specimens were
also in an active condition, and the circulation of granular matter in all was
distinctly visible. In the Pinnulariæ two large colourless vesicles were seen
on either side of the median nodule, each having a central nucleus, as
represented in the accompanying sketch, made while under observation in
two positions. The central portion of each frustule was closely packed with
a rich yellowish-brown coloured endochrome, interspersed with a few fat
globules. The phenomenon of cyclosis was not seen in any of these diatoms,
but I have satisfied myself, by staining, of the presence of a delicately fine
external protoplasmic covering in many diatoms. That their movements
resemble the gliding movements exhibited by the Amœba can scarcely be
doubted. Numerous forms of Diatomaceæ are found growing on or attached
to water-plants or pieces of detached stalks, which, although generally
simple, are sometimes compound, dividing and subdividing in a beautiful
ramous manner. Pinnulariæ, Nitzschia, &c., are seen adherent by one
extremity, about which they turn or bend themselves as on a hinge. By the
process of cell-division, groups of Synedræ become attached by a point, in
all that were in a healthy condition. I examined several, and watched them
for a long time. The phenomenon described depends much upon the healthy
condition of the frustule at the time; as the movements of the diatoms
became sluggish, the circulation gradually slackens and then ceases
altogether. I also saw a somewhat similar action in the more active
specimens of P. hippocampus and Navicula cuspidata, but the coarser
markings and thickness of the wall of these diatoms seemed to place greater
difficulties in the way of observation than the finer valves of the P.
angulatum. One thing I believe is certain, that the circulation described is
precisely similar to that seen in the Closteria, or, on a much larger scale, in
Chara and the leaf of the Anacharis, bearing in mind also that in the
Closterium the cell is divided by a transverse suture, and in P. angulatum by
a longitudinal one (Plate II., Nos. 38-40). About the same time some very
lively specimens of the Pinnulariæ were sent to me, and the movements of
these frustules were more closely observed. One or two of the more active
would attack a body relatively larger than itself, it would also force its way
into a mass of granular matter, and then recede from it with a jerky motion.
In more than one instance a cell of Palmoglæa was seized and carried away
by the Pinnularia, the former at the time being actively engaged in the
process of cell division. Other diatoms present among my specimens were
also in an active condition, and the circulation of granular matter in all was
distinctly visible. In the Pinnulariæ two large colourless vesicles were seen
on either side of the median nodule, each having a central nucleus, as
represented in the accompanying sketch, made while under observation in
two positions. The central portion of each frustule was closely packed with
a rich yellowish-brown coloured endochrome, interspersed with a few fat
globules. The phenomenon of cyclosis was not seen in any of these diatoms,
but I have satisfied myself, by staining, of the presence of a delicately fine
external protoplasmic covering in many diatoms. That their movements
resemble the gliding movements exhibited by the Amœba can scarcely be
doubted. Numerous forms of Diatomaceæ are found growing on or attached
to water-plants or pieces of detached stalks, which, although generally
simple, are sometimes compound, dividing and subdividing in a beautiful
ramous manner. Pinnulariæ, Nitzschia, &c., are seen adherent by one
extremity, about which they turn or bend themselves as on a hinge. By the
process of cell-division, groups of Synedræ become attached by a point, in
Page 508
a fan-like form. The fan-like collection of frustules is said to be flabellate,
or radiate. In Licmophora, Achnanthes and other species (Plate II., Nos. 29-
33) the double condition of union of frustules and of attachment by a
pedicle are illustrated. When a stipe branches it does so normally in a
dichotomous manner, each new individual being produced by a secondary
pedicle. This regular dichotomy is seen in several genera: Cocconema and
Gomphonema, the latter more perfectly in Fig. 296, from a
microphotograph, in which a branching, or rather longitudinal, rupture of
the pedicle takes place at intervals, and the entire organism presents a more
or less complete flabella, or fan-like cluster, on the summit of the branches,
and imperfect or single frustules irregularly scattered throughout the whole
length of the pedicle.
Isthmia enervis (Fig. 297).—The unicellular frustule of this species is
extremely difficult to define, owing to the large areolations of the valves; it
has a remarkable internal structure. The olive-brown cell contents are found
collected, for the most part, into a central mass, from which radiating,
branched, granular threads extend to and unite with the periphery. When
viewed by a magnifying power of 600 or 700 diameters, these
prolongations are seen to be composed of aggregations of ovate or spindle-
shaped corpuscles, held together by protoplasmic matter. These bodies are
sometimes quiescent, but more often travel slowly to and fro from the
central mass. The general aspect under these conditions so nearly
corresponds to the characteristic circulation in the frustules of unicellular
plants and of certain rhizopoda, that it is difficult to realise that the object
when under examination is an elegant marine diatom.
There is a large section of diatoms in which the frustules are diffused
throughout a muco-gelatinous envelope in a definite manner. Histologically
this is homologous with the pedicles and connecting nodules thrown out
during the act of self-division, and in some species (Cocconeis, Fragillaria,
&c.) it often persists after that act is complete.
or radiate. In Licmophora, Achnanthes and other species (Plate II., Nos. 29-
33) the double condition of union of frustules and of attachment by a
pedicle are illustrated. When a stipe branches it does so normally in a
dichotomous manner, each new individual being produced by a secondary
pedicle. This regular dichotomy is seen in several genera: Cocconema and
Gomphonema, the latter more perfectly in Fig. 296, from a
microphotograph, in which a branching, or rather longitudinal, rupture of
the pedicle takes place at intervals, and the entire organism presents a more
or less complete flabella, or fan-like cluster, on the summit of the branches,
and imperfect or single frustules irregularly scattered throughout the whole
length of the pedicle.
Isthmia enervis (Fig. 297).—The unicellular frustule of this species is
extremely difficult to define, owing to the large areolations of the valves; it
has a remarkable internal structure. The olive-brown cell contents are found
collected, for the most part, into a central mass, from which radiating,
branched, granular threads extend to and unite with the periphery. When
viewed by a magnifying power of 600 or 700 diameters, these
prolongations are seen to be composed of aggregations of ovate or spindle-
shaped corpuscles, held together by protoplasmic matter. These bodies are
sometimes quiescent, but more often travel slowly to and fro from the
central mass. The general aspect under these conditions so nearly
corresponds to the characteristic circulation in the frustules of unicellular
plants and of certain rhizopoda, that it is difficult to realise that the object
when under examination is an elegant marine diatom.
There is a large section of diatoms in which the frustules are diffused
throughout a muco-gelatinous envelope in a definite manner. Histologically
this is homologous with the pedicles and connecting nodules thrown out
during the act of self-division, and in some species (Cocconeis, Fragillaria,
&c.) it often persists after that act is complete.
Page 509
Fig. 297.—Isthmia enervis. Microphotograph.
Diatomaceæ, Recent and Fossil.
Fig. 298.—Fossil Diatoms from Springfield (Barbadoes).
1, Achnanthidium; 2, Diatoma vulgare, side view and front view; 3, Biddulphia; 4,
5, 6, 7, Amphitetias antediluviana, front view, with globular and oval forms;
Gomphonema elongatum and capitatum.
Diatomaceæ, Recent and Fossil.
Fig. 298.—Fossil Diatoms from Springfield (Barbadoes).
1, Achnanthidium; 2, Diatoma vulgare, side view and front view; 3, Biddulphia; 4,
5, 6, 7, Amphitetias antediluviana, front view, with globular and oval forms;
Gomphonema elongatum and capitatum.
Page 510
Fossilised Diatomaceæ.—Dr. Gregory was of opinion that a large number
of diatoms separated into species are only transition forms, and more
extended observations have proved that form and outline are not always to
be trusted in this matter. Species-making is a modern invention, and can
hardly apply to the indestructible fossilised forms of the frustules of
Diatomaceæ, with their beautiful sculpturings and geometrical
constructions, which have not been materially changed since they were first
deposited. Startling and almost incredible as the assertion may appear to
some, it is none the less a fact established beyond all question, that some of
the most gigantic mountain-ranges, as the mighty Andes, towering into
space 25,250 feet above the level of the sea, their base occupying vast areas
of land; as also massive limestone rocks; the sand that covers boundless
deserts; and the soil of many wide-extended plains, are each and all
principally composed of Diatomaceæ. And, as Dr. Buckland once observed:
“The remains of such minute animals have added much more to the mass of
materials which compose the exterior crust of the globe than the bones of
elephants, hippopotami, and whales.”
In 1841 the late Mr. Sollitt, of Hull, discovered the beautiful longitudinal
and transverse striæ (markings) on the Pleurosigma hippocampus. A curved
graceful line runs down the shell, in the centre of which is an expanded oval
opening. Near to the central opening the dots elongate crossways,
presenting the appearance of small short bands.
In the vicinity of this town many interesting varieties of Diatomaceæ have
been found, the beauty of the varied forms of which are constantly under
investigation; at the same time some of them are highly useful, as forming
that class of test objects which are better calculated than many others for
determining the excellence and powers of certain objectives. Mr. Sollitt
carefully measured the markings on some of the frustules and found they
ranged between the 1⁄30000th and 1⁄130000th of an inch; the Pleurosigma strigilis
having the strongest markings, and the Pleurosigma acus the finest.
Mr. J. D. Sollitt not only first proposed their use, but he also furnished the
measurements of the lines of the several members of this family, as follows:
—
of diatoms separated into species are only transition forms, and more
extended observations have proved that form and outline are not always to
be trusted in this matter. Species-making is a modern invention, and can
hardly apply to the indestructible fossilised forms of the frustules of
Diatomaceæ, with their beautiful sculpturings and geometrical
constructions, which have not been materially changed since they were first
deposited. Startling and almost incredible as the assertion may appear to
some, it is none the less a fact established beyond all question, that some of
the most gigantic mountain-ranges, as the mighty Andes, towering into
space 25,250 feet above the level of the sea, their base occupying vast areas
of land; as also massive limestone rocks; the sand that covers boundless
deserts; and the soil of many wide-extended plains, are each and all
principally composed of Diatomaceæ. And, as Dr. Buckland once observed:
“The remains of such minute animals have added much more to the mass of
materials which compose the exterior crust of the globe than the bones of
elephants, hippopotami, and whales.”
In 1841 the late Mr. Sollitt, of Hull, discovered the beautiful longitudinal
and transverse striæ (markings) on the Pleurosigma hippocampus. A curved
graceful line runs down the shell, in the centre of which is an expanded oval
opening. Near to the central opening the dots elongate crossways,
presenting the appearance of small short bands.
In the vicinity of this town many interesting varieties of Diatomaceæ have
been found, the beauty of the varied forms of which are constantly under
investigation; at the same time some of them are highly useful, as forming
that class of test objects which are better calculated than many others for
determining the excellence and powers of certain objectives. Mr. Sollitt
carefully measured the markings on some of the frustules and found they
ranged between the 1⁄30000th and 1⁄130000th of an inch; the Pleurosigma strigilis
having the strongest markings, and the Pleurosigma acus the finest.
Mr. J. D. Sollitt not only first proposed their use, but he also furnished the
measurements of the lines of the several members of this family, as follows:
—
Page 511
Amphipleura pellucida, or Acus, 130,000 in the inch, cross lines.
" sigmoidea, 70,000 in the inch.
Navicula rhomboides, 111,000 in the inch, cross lines.
Pleurosigma fasciola, fine shell, 86,000 in the inch, cross lines.
" " strong shell, 64,000 in the inch, cross lines.
" strigosum, 72,000 in the inch, diagonal lines.
" angulatum, 51,000 in the inch, diagonal lines.
" quadratum, 50,000 in the inch, diagonal lines.
" Spencerii, 50,000 in the inch, cross lines.
" attenuatum, 42,000 in the inch, cross lines.
" Balticum, 40,000 in the inch, cross lines.
" formosum, 32,000 in the inch, diagonal lines.
" strigilis, 30,000 in the inch, cross lines.
PLATE XII.
" sigmoidea, 70,000 in the inch.
Navicula rhomboides, 111,000 in the inch, cross lines.
Pleurosigma fasciola, fine shell, 86,000 in the inch, cross lines.
" " strong shell, 64,000 in the inch, cross lines.
" strigosum, 72,000 in the inch, diagonal lines.
" angulatum, 51,000 in the inch, diagonal lines.
" quadratum, 50,000 in the inch, diagonal lines.
" Spencerii, 50,000 in the inch, cross lines.
" attenuatum, 42,000 in the inch, cross lines.
" Balticum, 40,000 in the inch, cross lines.
" formosum, 32,000 in the inch, diagonal lines.
" strigilis, 30,000 in the inch, cross lines.
PLATE XII.
Page 512
MICRO-PHOTOGRAPH OF TEST DIATOMS.
Lichenaceæ.
The lichens are a family of autonomous plants, an intermediary group of
algals or cellular cryptogams, drawing their nourishment from the air
through their whole surface medium, and propagating by spores usually
enclosed in asci, and always having green gonidia in their thallus. Their
gonidia, bright coloured globular cells, form layers under the cortical
covering of the thallus, and generally develop in the form of incrustations,
which cover stones, wood, and the bark of trees, or penetrate into the
lamellæ of the epidermis of woody plants. The gonidia of lichens partake of
both the character of vegetative and reproductive cells.
The thallus in the fructicose group attaches itself by a narrow base, growing
in the form of a miniature shrub. Another group is met with in a slimy
condition—the gelatinous lichens. These species, for the most part,
furnished dyes before the discovery of the coal-tar dyes. In many of the
Palmella cruenta, commonly found growing on the walls and roofs of
houses, a colourless acid liquid is found, which, on being treated with
alkali, produces a bright yellow colour; and another, Avernia vulpina,
furnishes a brown dye; the Rocella fuciformis and R. tinctoria yield the
purple dye substance known as orchil, or archil, from which the useful blue
paper of the chemist for testing acidity is manufactured. Usnic acid,
combined with green and yellow resins, seems to be more or less a
constituent of many lichens.
A vertical section of Palmella stellata is given in Plate I., No. 26, in which
the emission of the ripe spores of the lichens is seen to be not unlike that
which takes place in some of the fungi, Pezizæ, Sphæriæ, &c. If a portion
of the thallus be moistened and placed in a common phial, with the
apotheca turned toward one side, in a few hours the opposite surface of the
glass will be found covered with patches of spores, easily perceptible by
their colour; or if placed on a moistened surface, and one of the usual glass
slips laid over it, the latter will be covered in a short time. As to the powers
of dissemination of these lowly organised plants, an observation led to the
Lichenaceæ.
The lichens are a family of autonomous plants, an intermediary group of
algals or cellular cryptogams, drawing their nourishment from the air
through their whole surface medium, and propagating by spores usually
enclosed in asci, and always having green gonidia in their thallus. Their
gonidia, bright coloured globular cells, form layers under the cortical
covering of the thallus, and generally develop in the form of incrustations,
which cover stones, wood, and the bark of trees, or penetrate into the
lamellæ of the epidermis of woody plants. The gonidia of lichens partake of
both the character of vegetative and reproductive cells.
The thallus in the fructicose group attaches itself by a narrow base, growing
in the form of a miniature shrub. Another group is met with in a slimy
condition—the gelatinous lichens. These species, for the most part,
furnished dyes before the discovery of the coal-tar dyes. In many of the
Palmella cruenta, commonly found growing on the walls and roofs of
houses, a colourless acid liquid is found, which, on being treated with
alkali, produces a bright yellow colour; and another, Avernia vulpina,
furnishes a brown dye; the Rocella fuciformis and R. tinctoria yield the
purple dye substance known as orchil, or archil, from which the useful blue
paper of the chemist for testing acidity is manufactured. Usnic acid,
combined with green and yellow resins, seems to be more or less a
constituent of many lichens.
A vertical section of Palmella stellata is given in Plate I., No. 26, in which
the emission of the ripe spores of the lichens is seen to be not unlike that
which takes place in some of the fungi, Pezizæ, Sphæriæ, &c. If a portion
of the thallus be moistened and placed in a common phial, with the
apotheca turned toward one side, in a few hours the opposite surface of the
glass will be found covered with patches of spores, easily perceptible by
their colour; or if placed on a moistened surface, and one of the usual glass
slips laid over it, the latter will be covered in a short time. As to the powers
of dissemination of these lowly organised plants, an observation led to the
Page 513
conclusion that the gonidia of lichens have greater powers in this direction
than was formerly supposed. It is found that by placing a clean sheet of
glass in the open air during a fall of snow, and receiving the melting water
in a tube or bottle, quantities of what has been looked upon as a “unicellular
plant” can be taken, the cells of which may be kept in a dormant condition
for a long time during cold weather, but upon the return of spring warmth
and moisture they begin to increase, by a process of subdivision, into two,
four or eight portions; these soon assume a rounded form, and burst the
parent cell-wall open; these secondary cells then begin to divide and
subdivide again, and the process may go on without much variation for a
long time. The phenomena described may be watched by taking a portion of
the bark of a tree on which Chlorococcus has been deposited, and placing it
under a glass to keep it in a moderately moist atmosphere; the only
difference being a change in colour, caused by the growth of the fibres, as
may be seen on microscopical examination. “And this,” says Dr. Hicks,
who first observed this phenomenon in plant life, “is an instructive point,
because it will be found that the colour varies notably according to the
lichen prevalent in its neighbourhood.”59 He believes there can be no doubt
that what has been called Chlorococcus is nothing more than the gonidia of
a lichen; and that under suitable conditions, chiefly drought and warmth, the
gonidium often throws out from its external envelope a small fibre, which,
adhering and branching, forms a “soridium.” “The soridia remain dormant
for a very long time, and do not develop into thalli unless in a favourable
situation, in some cases it may be for years. It will be perceived that the
soridium contains all the elements of a thallus in miniature; in fact, a thallus
does frequently arise from one alone, and the fibres of neighbouring soridia
interlace; thus a thallus is matured very rapidly. This is one of the causes of
the variation of appearance so common in many species of lichens, more
readily seen towards the centre of the parent thallus. When the gonidia
remain attached to the parent thallus, the circumstances are, of course, more
favourable, and they develop into secondary thalli, attached more or less to
the older one, which, in many instances, decays beneath them. This process
being continued year after year gives an apparent thickness and spongy
appearance to the lichen, and is the principal cause of the various
modifications in the external aspect of the lichens which caused them
formerly to be misunderstood and wrongly classified.”60
than was formerly supposed. It is found that by placing a clean sheet of
glass in the open air during a fall of snow, and receiving the melting water
in a tube or bottle, quantities of what has been looked upon as a “unicellular
plant” can be taken, the cells of which may be kept in a dormant condition
for a long time during cold weather, but upon the return of spring warmth
and moisture they begin to increase, by a process of subdivision, into two,
four or eight portions; these soon assume a rounded form, and burst the
parent cell-wall open; these secondary cells then begin to divide and
subdivide again, and the process may go on without much variation for a
long time. The phenomena described may be watched by taking a portion of
the bark of a tree on which Chlorococcus has been deposited, and placing it
under a glass to keep it in a moderately moist atmosphere; the only
difference being a change in colour, caused by the growth of the fibres, as
may be seen on microscopical examination. “And this,” says Dr. Hicks,
who first observed this phenomenon in plant life, “is an instructive point,
because it will be found that the colour varies notably according to the
lichen prevalent in its neighbourhood.”59 He believes there can be no doubt
that what has been called Chlorococcus is nothing more than the gonidia of
a lichen; and that under suitable conditions, chiefly drought and warmth, the
gonidium often throws out from its external envelope a small fibre, which,
adhering and branching, forms a “soridium.” “The soridia remain dormant
for a very long time, and do not develop into thalli unless in a favourable
situation, in some cases it may be for years. It will be perceived that the
soridium contains all the elements of a thallus in miniature; in fact, a thallus
does frequently arise from one alone, and the fibres of neighbouring soridia
interlace; thus a thallus is matured very rapidly. This is one of the causes of
the variation of appearance so common in many species of lichens, more
readily seen towards the centre of the parent thallus. When the gonidia
remain attached to the parent thallus, the circumstances are, of course, more
favourable, and they develop into secondary thalli, attached more or less to
the older one, which, in many instances, decays beneath them. This process
being continued year after year gives an apparent thickness and spongy
appearance to the lichen, and is the principal cause of the various
modifications in the external aspect of the lichens which caused them
formerly to be misunderstood and wrongly classified.”60
Page 514
The erratic lichens are found among the genus Palmella, some of which
grow among boulders of the primary and metamorphic formations, curled
up into a ball, and only fixed to their matrix by a slender thread. The
globular Lecanora esculenta will at times suddenly cover large tracts of
country in Persia and Tartary, where it is eaten by the cattle. During a
scarcity of food a shower of these lichens, Mr. Berkeley tells us, fell at
Erzeroum, and saved the cattle from starvation.61
Another group of the Palmella, or Peltigeri, so named from the target-like
discs on their surface, spread their foliaceous fronds over the ground, and as
the fruit is marginal, it gives the thallus a digitate appearance. These are
often spotted over by a little red fungus. The Lecidinei contains numerous
species of the most varied habits, and always crustaceous, and so closely
adherent to the hard rocks and stones on which they grow, that at length
they disintegrate them. From this low species a higher form arises, with
erect branching stems, and clothed with foliaceous, brightly-coloured
scales.
The Coccocarpei is mainly distinguished by having orbicular discs entirely
deprived of the cortical envelope called an excipulum. The discs spring at
once from the medullary stratum, and contain asci and sporidia similar to
those of the minute fungi Sphæriæ. Some of the lichens are themselves
parasitic, and begin existence under the thick skin of the leaves of tropical
plants, and spread encrusting thallus over their surface, the excipulum and
perithecia being black; but in most cases these are beautifully sculptured,
and are interesting objects for the microscope. Indeed, the sphere-bearing
lichens, with upright stems bearing globular fruit at the extremity of their
branches, are at first indicated by a swelling, but in time the outer layer
bursts and exposes sporidia, which are beautiful objects under the
microscope on account of their spherical form and more or less deep blue
tint. Humble and lowly as lichens may appear to be, they have been divided
into fifty-eight or more genera and 2,500 species. The brothers Tulasne, De
Bary, the Rev. Mr. Berkeley, and others, devoted great attention to the
peculiarities of their structure and natural history.
Hepaticæ.—An intermediary group of much interest to the microscopist are
the Hepaticæ (liverworts). These are found growing on damp rocks in the
grow among boulders of the primary and metamorphic formations, curled
up into a ball, and only fixed to their matrix by a slender thread. The
globular Lecanora esculenta will at times suddenly cover large tracts of
country in Persia and Tartary, where it is eaten by the cattle. During a
scarcity of food a shower of these lichens, Mr. Berkeley tells us, fell at
Erzeroum, and saved the cattle from starvation.61
Another group of the Palmella, or Peltigeri, so named from the target-like
discs on their surface, spread their foliaceous fronds over the ground, and as
the fruit is marginal, it gives the thallus a digitate appearance. These are
often spotted over by a little red fungus. The Lecidinei contains numerous
species of the most varied habits, and always crustaceous, and so closely
adherent to the hard rocks and stones on which they grow, that at length
they disintegrate them. From this low species a higher form arises, with
erect branching stems, and clothed with foliaceous, brightly-coloured
scales.
The Coccocarpei is mainly distinguished by having orbicular discs entirely
deprived of the cortical envelope called an excipulum. The discs spring at
once from the medullary stratum, and contain asci and sporidia similar to
those of the minute fungi Sphæriæ. Some of the lichens are themselves
parasitic, and begin existence under the thick skin of the leaves of tropical
plants, and spread encrusting thallus over their surface, the excipulum and
perithecia being black; but in most cases these are beautifully sculptured,
and are interesting objects for the microscope. Indeed, the sphere-bearing
lichens, with upright stems bearing globular fruit at the extremity of their
branches, are at first indicated by a swelling, but in time the outer layer
bursts and exposes sporidia, which are beautiful objects under the
microscope on account of their spherical form and more or less deep blue
tint. Humble and lowly as lichens may appear to be, they have been divided
into fifty-eight or more genera and 2,500 species. The brothers Tulasne, De
Bary, the Rev. Mr. Berkeley, and others, devoted great attention to the
peculiarities of their structure and natural history.
Hepaticæ.—An intermediary group of much interest to the microscopist are
the Hepaticæ (liverworts). These are found growing on damp rocks in the
Page 515
neighbourhood of springs and dripping banks. The scale-moss, the
Marchantia polymorphia (Fig. 299), may be taken as typical of this little
group, with its gemmiparous conceptacles and lobed receptacles, bearing
archegones on transparent glass-like fruit stalks, carrying on their summits
either round shield-like discs or radiating bodies with a striking
resemblance to a wheel without its tyre.
The liverworts are closely allied to the
mosses, and as much difficulty was
experienced in dividing the two, Hooker
placed the whole under one genus, the
Jungermannia. More recently, however,
they have been divided into those with a
stem and leaves confluent in a frond,
Fig. 299.—Marchantia polymorphia. Marchantia; those with stem and leaves
distinct, Jungermannia; and those with a
solitary capsule, filiform, bivalved, stalked, with a free central placentation,
Anthocotaceæ. Some botanists have further divided them, but they are all
extensively propagated by gemmæ.
The fronds carry the male organs, or antherids, and the disc, in the first
instance, bears the female organs, or archegones, and after a time gives
place to the sporanges, or spore cases. It is these bodies which are of so
much interest to microscopists; if the plant is brought into a warm room,
they suddenly burst open with some violence the moment a drop of water is
applied to them, and the sporanges are dispersed in a small cloud of
brownish dust. If this dust is examined under a medium power, it is seen to
consist of a number of chain-like bodies, somewhat like the spring of a
small watch; and if the process of bursting be closely watched, these minute
springs will be found twisting and curling about in every direction. The
structure of the frond itself will be seen to be interesting when cut in the
vertical direction and placed under the microscope.
The gemmæ of Marchantia polymorphia are produced in elegant
membranous cups, with a toothed margin growing on the upper surface of
the frond, especially in very damp courtyards between the stones, or near
running water, where its lobed fronds are found covering extensive tracts of
Marchantia polymorphia (Fig. 299), may be taken as typical of this little
group, with its gemmiparous conceptacles and lobed receptacles, bearing
archegones on transparent glass-like fruit stalks, carrying on their summits
either round shield-like discs or radiating bodies with a striking
resemblance to a wheel without its tyre.
The liverworts are closely allied to the
mosses, and as much difficulty was
experienced in dividing the two, Hooker
placed the whole under one genus, the
Jungermannia. More recently, however,
they have been divided into those with a
stem and leaves confluent in a frond,
Fig. 299.—Marchantia polymorphia. Marchantia; those with stem and leaves
distinct, Jungermannia; and those with a
solitary capsule, filiform, bivalved, stalked, with a free central placentation,
Anthocotaceæ. Some botanists have further divided them, but they are all
extensively propagated by gemmæ.
The fronds carry the male organs, or antherids, and the disc, in the first
instance, bears the female organs, or archegones, and after a time gives
place to the sporanges, or spore cases. It is these bodies which are of so
much interest to microscopists; if the plant is brought into a warm room,
they suddenly burst open with some violence the moment a drop of water is
applied to them, and the sporanges are dispersed in a small cloud of
brownish dust. If this dust is examined under a medium power, it is seen to
consist of a number of chain-like bodies, somewhat like the spring of a
small watch; and if the process of bursting be closely watched, these minute
springs will be found twisting and curling about in every direction. The
structure of the frond itself will be seen to be interesting when cut in the
vertical direction and placed under the microscope.
The gemmæ of Marchantia polymorphia are produced in elegant
membranous cups, with a toothed margin growing on the upper surface of
the frond, especially in very damp courtyards between the stones, or near
running water, where its lobed fronds are found covering extensive tracts of
Page 516
moist soil. At the period of
fructification the fronds send up
stalks, which carry at their
summit round shield-like
radiating discs, which bear upon
their surface a number of little
open basket-shaped
“conceptacles.” These again
expand into singularly graceful
cups (as in Fig. 300), and are Fig. 300.—Gemmiparous conceptacle of Marchantia
found in all stages of polymorphia, expanding and rising from the
surface of a frond. In the interior are seen
development. When mature, the gopidial gemmæ already detached by the splitting
basket contains a number of little of the epiderm.
green round or oblong discs, each
composed of two or more layers of cells; the wall itself being surmounted
by a glistening fringe of teeth, whose edges are themselves regularly
fringed with minute outgrowths. The cup seems to be formed by a
development of the superior epidermis, which is raised up, and finally
bursts and spreads out, laying bare the seeds.
The archegones of Marchantia are very curious bodies, while the elater and
spores are even still more so. These are elongated cells, each containing a
double spiral fibre coiled up in the interior. It is the elasticity of this which
tears apart the cell-membrane, and sends forth the spores with a jerk, and
thus assists in their dispersion. Marchantia is the type of the malloid
Hepaticæ.
Musci, Bryophyta.
Mosses are a beautiful class of non-vascular cryptogams. Linnæus called
them servi, servants or workmen, as they seem to labour to produce
vegetation in places where soil is not already formed. The Bryophyta form
three natural divisions: the Bryinæ, or true mosses; the Sphagnaceæ, or
peat-mosses; and the Hepaticæ, or liverworts. The two first are commonly
united. In these the sexual organs consist of antheridia and archegonia, but
fructification the fronds send up
stalks, which carry at their
summit round shield-like
radiating discs, which bear upon
their surface a number of little
open basket-shaped
“conceptacles.” These again
expand into singularly graceful
cups (as in Fig. 300), and are Fig. 300.—Gemmiparous conceptacle of Marchantia
found in all stages of polymorphia, expanding and rising from the
surface of a frond. In the interior are seen
development. When mature, the gopidial gemmæ already detached by the splitting
basket contains a number of little of the epiderm.
green round or oblong discs, each
composed of two or more layers of cells; the wall itself being surmounted
by a glistening fringe of teeth, whose edges are themselves regularly
fringed with minute outgrowths. The cup seems to be formed by a
development of the superior epidermis, which is raised up, and finally
bursts and spreads out, laying bare the seeds.
The archegones of Marchantia are very curious bodies, while the elater and
spores are even still more so. These are elongated cells, each containing a
double spiral fibre coiled up in the interior. It is the elasticity of this which
tears apart the cell-membrane, and sends forth the spores with a jerk, and
thus assists in their dispersion. Marchantia is the type of the malloid
Hepaticæ.
Musci, Bryophyta.
Mosses are a beautiful class of non-vascular cryptogams. Linnæus called
them servi, servants or workmen, as they seem to labour to produce
vegetation in places where soil is not already formed. The Bryophyta form
three natural divisions: the Bryinæ, or true mosses; the Sphagnaceæ, or
peat-mosses; and the Hepaticæ, or liverworts. The two first are commonly
united. In these the sexual organs consist of antheridia and archegonia, but
Page 517
they are of simpler structure than will be found in ferns; and the first
generation from the spore is asexual.
The common or wall screw-moss
(Fig. 301) grows almost everywhere,
and if examined closely, is seen to
have springing from its base
numerous very slender stems, each
terminating in a dark brown case,
which encloses antheroids. If a patch
of the moss is gathered when in this
Fig. 301.—Screw-moss. state, and the green part of the base is
put into water, the threads of the
fringe will uncoil and disentangle themselves in a most curious and
beautiful manner; from this circumstance the plant takes its popular name of
screw-moss. The leaf usually consists of either a single or a double layer of
cells, having flattened sides, by which they adhere one to another. The leaf-
cells (Fig. 302) of the Sphagnum or bog-moss exhibit a curious departure
from the ordinary type; they are large, polygonal, and elongated, and
contain spiral fibres loosely coiled in their interior. The young leaf does not
differ from the older; both are evolved by a gradual process of
differentiation.
Mosses, like liverworts, possess
both antheridia and pistillida,
which are engaged in the process
of fructification. The fertilized
cell becomes gradually
developed into a conical body
elevated upon a footstalk, the
walls of the flask-shaped body
carrying the higher part upwards
as a calyptra or hood upon its
summit, while the lower part
Fig. 302.—Section of leaf of Sphagnum moss,
showing large cells of spiral fibres and remains to form a kind of collar
connecting apertures. round the base. These spore-
capsules are closed on their
generation from the spore is asexual.
The common or wall screw-moss
(Fig. 301) grows almost everywhere,
and if examined closely, is seen to
have springing from its base
numerous very slender stems, each
terminating in a dark brown case,
which encloses antheroids. If a patch
of the moss is gathered when in this
Fig. 301.—Screw-moss. state, and the green part of the base is
put into water, the threads of the
fringe will uncoil and disentangle themselves in a most curious and
beautiful manner; from this circumstance the plant takes its popular name of
screw-moss. The leaf usually consists of either a single or a double layer of
cells, having flattened sides, by which they adhere one to another. The leaf-
cells (Fig. 302) of the Sphagnum or bog-moss exhibit a curious departure
from the ordinary type; they are large, polygonal, and elongated, and
contain spiral fibres loosely coiled in their interior. The young leaf does not
differ from the older; both are evolved by a gradual process of
differentiation.
Mosses, like liverworts, possess
both antheridia and pistillida,
which are engaged in the process
of fructification. The fertilized
cell becomes gradually
developed into a conical body
elevated upon a footstalk, the
walls of the flask-shaped body
carrying the higher part upwards
as a calyptra or hood upon its
summit, while the lower part
Fig. 302.—Section of leaf of Sphagnum moss,
showing large cells of spiral fibres and remains to form a kind of collar
connecting apertures. round the base. These spore-
capsules are closed on their
Page 518
summit by opercula or lids, and their mouths when laid open are
surrounded by a beautiful toothed fringe, termed the peristome. This fringe
is shown in Fig. 303, in the centre of a capsule of Funaria, with its
peristome in situ. The fringes of teeth are variously constructed, and are of
great service in discriminating the genera. In Neckera antipyretica the
peristome is double, the inner being composed of teeth united by cross bars,
forming a very pretty trellis. The seed spores are contained in the upper part
of the capsule, where they are clustered round the central pillar, termed the
columella; and at the time of maturity, the interior of the capsule is almost
entirely occupied by spores.
Fig. 303.—Mouth of Capsule of Funaria, showing Fig. 304.—Hair-moss in
Peristome. Fruit.
The undulating hair-moss, Polytrichum undulatum (Fig. 304), is found on
moist, shady banks of pools and rivulets. The seed-vessel has a curious
surrounded by a beautiful toothed fringe, termed the peristome. This fringe
is shown in Fig. 303, in the centre of a capsule of Funaria, with its
peristome in situ. The fringes of teeth are variously constructed, and are of
great service in discriminating the genera. In Neckera antipyretica the
peristome is double, the inner being composed of teeth united by cross bars,
forming a very pretty trellis. The seed spores are contained in the upper part
of the capsule, where they are clustered round the central pillar, termed the
columella; and at the time of maturity, the interior of the capsule is almost
entirely occupied by spores.
Fig. 303.—Mouth of Capsule of Funaria, showing Fig. 304.—Hair-moss in
Peristome. Fruit.
The undulating hair-moss, Polytrichum undulatum (Fig. 304), is found on
moist, shady banks of pools and rivulets. The seed-vessel has a curious
Page 519
shaggy cap; but in its construction it is very similar to that of the screw-
moss, except that the fringe around its opening is not twisted. The
reproductive organs of mosses are of two kinds; the capsule containing
minute spores, archegonia, and the antheridia, or male efflorescence. The
capsule, theca, or sporangium, is lateral or terminal, sessile, or on a fruit
stalk (seta) of various shapes, indehiscent, or bursting by four valves at the
sides, or more commonly by a deciduous cup, operculum. When this falls
the mouth of the capsule becomes exposed. The rim is crowned with tooth-
like or cilia-like appendages in sets of four or multiples of that number—
peristome. These are often brightly coloured and hydroscopic. By simply
breathing upon them they suddenly fly open, and are endowed with motion,
that is, if they contain spores. The spores on germination produce a green
confervoid-like mass of threads, from which the young plant arises.
The Sphagnaceæ, or “bog mosses,” have been separated from true mosses
from the marked differences they present. The stem is more widely
differentiated, and throughout its structure a rapid passage of fluid takes
place. It has the power of absorbing moisture from the atmosphere, so that
if a plant be placed dry in a glass of water with its rosette of leaves hanging
over the edge, it acts like a syphon, and the water will drop from it until the
glass is emptied. As may be supposed, the leaf is composed of large open
cells, and it absorbs more water than the root. The antherids or male organs
of Sphagnaceæ resemble those of liverworts, rather than those of mosses,
both in form and arrangement; they are grouped in “catkins” at the tips of
the lateral branches, each of the imbricated perigonal leaves enclosing a
single globose antherid on a slender foot-stalk, and surrounded by long
branched paraphyses of cobweb-like tenuity. The female organs, or
archegones, do not differ materially in structure from those of mosses; they
are grouped together in a sheath of deep green leaves at the end of the
shorter lateral branchlets at the side of the rosette or terminal crown of
leaves. The sporange is very uniform in all the species, and the spores are in
groups of fours, as in mosses, around a hemispherical columella. These
plants grow so rapidly that they soon cover a pool with thin matted bundles
of branches, and as they decay they fall to the bottom, and become the
foundation of the future bog or peat moss.
moss, except that the fringe around its opening is not twisted. The
reproductive organs of mosses are of two kinds; the capsule containing
minute spores, archegonia, and the antheridia, or male efflorescence. The
capsule, theca, or sporangium, is lateral or terminal, sessile, or on a fruit
stalk (seta) of various shapes, indehiscent, or bursting by four valves at the
sides, or more commonly by a deciduous cup, operculum. When this falls
the mouth of the capsule becomes exposed. The rim is crowned with tooth-
like or cilia-like appendages in sets of four or multiples of that number—
peristome. These are often brightly coloured and hydroscopic. By simply
breathing upon them they suddenly fly open, and are endowed with motion,
that is, if they contain spores. The spores on germination produce a green
confervoid-like mass of threads, from which the young plant arises.
The Sphagnaceæ, or “bog mosses,” have been separated from true mosses
from the marked differences they present. The stem is more widely
differentiated, and throughout its structure a rapid passage of fluid takes
place. It has the power of absorbing moisture from the atmosphere, so that
if a plant be placed dry in a glass of water with its rosette of leaves hanging
over the edge, it acts like a syphon, and the water will drop from it until the
glass is emptied. As may be supposed, the leaf is composed of large open
cells, and it absorbs more water than the root. The antherids or male organs
of Sphagnaceæ resemble those of liverworts, rather than those of mosses,
both in form and arrangement; they are grouped in “catkins” at the tips of
the lateral branches, each of the imbricated perigonal leaves enclosing a
single globose antherid on a slender foot-stalk, and surrounded by long
branched paraphyses of cobweb-like tenuity. The female organs, or
archegones, do not differ materially in structure from those of mosses; they
are grouped together in a sheath of deep green leaves at the end of the
shorter lateral branchlets at the side of the rosette or terminal crown of
leaves. The sporange is very uniform in all the species, and the spores are in
groups of fours, as in mosses, around a hemispherical columella. These
plants grow so rapidly that they soon cover a pool with thin matted bundles
of branches, and as they decay they fall to the bottom, and become the
foundation of the future bog or peat moss.
Page 520
Felices.—Of all the spore-bearing families the ferns are the more
universally known. They constitute an exceedingly numerous genera and
species, and vary from low herbaceous plants of an inch in height to that of
tree ferns, which attain a height of fifty or more feet, terminating in a
graceful coronet of fronds or leaves. Of whatever size a fern may be, its
spores are, for the most part, microscopic, produced within the sporangium
by cell division, and are therefore free and variously shaped.
The true mode of development of ferns from their spores was that furnished
by Nägeli, who announced the existence of antheridia. On the spore starting
into life it sends out from the cell-wall of its outer coat a white tubular
projection, or root fibre (Fig. 305, A, B, and C), which passes through the
cell-wall of its outer coat. This attracts sufficient moisture to burst open the
outer, and then it begins to increase by the subdivision of its cells, until the
primary green prothallus D is formed. This falls to the ground, and, being
furnished on its under side with thread-like fibres, fixes itself to the earth,
and thus is developed the rhizome, or root of the future plant. In each of the
antheridia, which are numerous, a cell is formed, chiefly filled with
albuminous matter and free spores, each having attached a flat ribbon-like
filament, or stermatoid, curled in a spiral manner. These are ultimately set
free by the rupture of the cell-wall, and commence revolving rapidly by the
agency of the whip-like appendage at the larger end.
universally known. They constitute an exceedingly numerous genera and
species, and vary from low herbaceous plants of an inch in height to that of
tree ferns, which attain a height of fifty or more feet, terminating in a
graceful coronet of fronds or leaves. Of whatever size a fern may be, its
spores are, for the most part, microscopic, produced within the sporangium
by cell division, and are therefore free and variously shaped.
The true mode of development of ferns from their spores was that furnished
by Nägeli, who announced the existence of antheridia. On the spore starting
into life it sends out from the cell-wall of its outer coat a white tubular
projection, or root fibre (Fig. 305, A, B, and C), which passes through the
cell-wall of its outer coat. This attracts sufficient moisture to burst open the
outer, and then it begins to increase by the subdivision of its cells, until the
primary green prothallus D is formed. This falls to the ground, and, being
furnished on its under side with thread-like fibres, fixes itself to the earth,
and thus is developed the rhizome, or root of the future plant. In each of the
antheridia, which are numerous, a cell is formed, chiefly filled with
albuminous matter and free spores, each having attached a flat ribbon-like
filament, or stermatoid, curled in a spiral manner. These are ultimately set
free by the rupture of the cell-wall, and commence revolving rapidly by the
agency of the whip-like appendage at the larger end.
Page 521
Fig. 305.—Development of the Globular Antheridium and Spermatoids of Pteris
serrulata.
A. Spores; B, C. Early stages of development; D. Prothallus with radial fibres; a, a
and a, b are stermatoids; and h, h. Enclosed antheridia.
The sporangia, or spore-cases, are, for the most part, globular in form, and
are nearly or quite surrounded by a strong elastic ring, which in some cases
is continued to form a stalk. When the spores are ripe, this ring, by its
elastic force, tears open the sporangia and gives exit to a quantity of
microscopic filaments, curled in corkscrew-like fashion (Figs. 305 and
307). The ring assumes various forms; in one group it passes vertically up
the back of the sporangium, and is continued to a point termed the stomata,
where the horizontal bursting takes place. This form is seen in Fig. 306, a,
b. In other groups it is vertical, as in c, c; in others transverse, as in d; or
apical, as at e; and in a few instances it is obsolete, as in f. These are the
true ferns, and their systematic arrangement is chiefly founded on the
peculiarity of the sori and sporangia, characters which become quite
intelligible by the aid of the microscope.
serrulata.
A. Spores; B, C. Early stages of development; D. Prothallus with radial fibres; a, a
and a, b are stermatoids; and h, h. Enclosed antheridia.
The sporangia, or spore-cases, are, for the most part, globular in form, and
are nearly or quite surrounded by a strong elastic ring, which in some cases
is continued to form a stalk. When the spores are ripe, this ring, by its
elastic force, tears open the sporangia and gives exit to a quantity of
microscopic filaments, curled in corkscrew-like fashion (Figs. 305 and
307). The ring assumes various forms; in one group it passes vertically up
the back of the sporangium, and is continued to a point termed the stomata,
where the horizontal bursting takes place. This form is seen in Fig. 306, a,
b. In other groups it is vertical, as in c, c; in others transverse, as in d; or
apical, as at e; and in a few instances it is obsolete, as in f. These are the
true ferns, and their systematic arrangement is chiefly founded on the
peculiarity of the sori and sporangia, characters which become quite
intelligible by the aid of the microscope.
Page 522
The beautiful ringed sporangium of
the fern (Fig. 307) when ruptured
gives exit to the dust-like spores;
these, examined under a moderate
power, are seen to be sub-globose
and pyramidal, the outer coat or
exospore being a coloured hyaline
cell with nuclei similar to the spores
of mosses, but in which chlorophyll
soon begins to form, and from this
little green embryonic growth the
organs of reproduction are formed.
Fig. 306.—Sporangia of Polypodiaceous
Ferns. In all ferns the pistillidia or
a, b. Polypodiaceæ; c. Cyantheineæ; d. archegonia are analogous to the
Gleichenineæ; e. Schizeineæ; f. Osmundineæ. ovules or nascent seeds of flowering
plants, and contain, like them, a
germinal vesicle, which becomes fertilized
through the agency of the spiral filaments,
and then gradually develops into an embryo
plant possessing a terminal bud. This bud
begins at once to unfold and push out leaves
with a circinate vernation, of a very simple
form at first, and growing up beneath the
prothallium, coming out at the notch; single
fibrous roots are at the same time sent down
into the earth, the delicate expanded
Fig. 307.—Spores of Deparia prolifera.
prothallium withers away, and the
foundation of the perfect fern plant is laid.
When a fern acquires a considerable stem, as in a tree fern, it consists of
cellular tissue and an external cortical portion forming fibro-vascular
bundles, scalariform ducts, and woody fibre. Fig. 308, b, shows an oblique
section of the footstalk of a fern leaf with its bundle of scalariform ducts.
These observations on ferns have acquired increased interest from
subsequent investigations made on the allied Cryptogams, and on the
processes occurring in the impregnation of the Conifers. Not only have later
the fern (Fig. 307) when ruptured
gives exit to the dust-like spores;
these, examined under a moderate
power, are seen to be sub-globose
and pyramidal, the outer coat or
exospore being a coloured hyaline
cell with nuclei similar to the spores
of mosses, but in which chlorophyll
soon begins to form, and from this
little green embryonic growth the
organs of reproduction are formed.
Fig. 306.—Sporangia of Polypodiaceous
Ferns. In all ferns the pistillidia or
a, b. Polypodiaceæ; c. Cyantheineæ; d. archegonia are analogous to the
Gleichenineæ; e. Schizeineæ; f. Osmundineæ. ovules or nascent seeds of flowering
plants, and contain, like them, a
germinal vesicle, which becomes fertilized
through the agency of the spiral filaments,
and then gradually develops into an embryo
plant possessing a terminal bud. This bud
begins at once to unfold and push out leaves
with a circinate vernation, of a very simple
form at first, and growing up beneath the
prothallium, coming out at the notch; single
fibrous roots are at the same time sent down
into the earth, the delicate expanded
Fig. 307.—Spores of Deparia prolifera.
prothallium withers away, and the
foundation of the perfect fern plant is laid.
When a fern acquires a considerable stem, as in a tree fern, it consists of
cellular tissue and an external cortical portion forming fibro-vascular
bundles, scalariform ducts, and woody fibre. Fig. 308, b, shows an oblique
section of the footstalk of a fern leaf with its bundle of scalariform ducts.
These observations on ferns have acquired increased interest from
subsequent investigations made on the allied Cryptogams, and on the
processes occurring in the impregnation of the Conifers. Not only have later
Page 523
researches furnished a satisfactory interpretation of the archegonia and
antheridia of the mosses and liverworts, but they have made known and co-
ordinated the existence of analogous phenomena in the Equisetaceæ,
Lycopodiaceæ, and Rhizocarpeæ, and prove, moreover, that the bodies
described by Dr. Brown in the Conifers under the name of “corpuscles” are
analogous to the archegonia of the Cryptogams; so that a link is hereby
formed between these groups and the higher flowering plants.
Fig. 308.—a. Vertical section of Fern-root, showing spiral tissue and cells filled
with granular bodies; b. Section of Footstalk.
Equisetaceæ.—The development of Horse-tails (Fig. 309), the name by
which they are commonly known, corresponds in some respects with that of
ferns. They comprise a little group, and the whole of their structure is
composed in an extraordinary degree by silex, so that even when the
organic portion has been destroyed by prolonged maceration in strong acid,
a consistent skeleton still remains. It is this flinty material that constitutes
their chief interest for microscopists. A portion of their silicious particles is
distributed in two lines, arranged parallel to the axis of the plant, others are
grouped into oval forms, and connected by a chain as in a necklace. The
form and arrangement of the crystals are better seen under polarised light.
Plate VIII., No. 170, a portion of the epidermis, forms an extremely
beautiful object. Sir David Brewster pointed out that each silicious particle
has a regular axis of double refraction. What is usually said to be the
fructification of the Equisetaceæ forms a cone or spike-like extremity to the
antheridia of the mosses and liverworts, but they have made known and co-
ordinated the existence of analogous phenomena in the Equisetaceæ,
Lycopodiaceæ, and Rhizocarpeæ, and prove, moreover, that the bodies
described by Dr. Brown in the Conifers under the name of “corpuscles” are
analogous to the archegonia of the Cryptogams; so that a link is hereby
formed between these groups and the higher flowering plants.
Fig. 308.—a. Vertical section of Fern-root, showing spiral tissue and cells filled
with granular bodies; b. Section of Footstalk.
Equisetaceæ.—The development of Horse-tails (Fig. 309), the name by
which they are commonly known, corresponds in some respects with that of
ferns. They comprise a little group, and the whole of their structure is
composed in an extraordinary degree by silex, so that even when the
organic portion has been destroyed by prolonged maceration in strong acid,
a consistent skeleton still remains. It is this flinty material that constitutes
their chief interest for microscopists. A portion of their silicious particles is
distributed in two lines, arranged parallel to the axis of the plant, others are
grouped into oval forms, and connected by a chain as in a necklace. The
form and arrangement of the crystals are better seen under polarised light.
Plate VIII., No. 170, a portion of the epidermis, forms an extremely
beautiful object. Sir David Brewster pointed out that each silicious particle
has a regular axis of double refraction. What is usually said to be the
fructification of the Equisetaceæ forms a cone or spike-like extremity to the
Page 524
top of the stem (Fig. 309), the whole resembling a series of spike-like
branches (the real stem being a horizontal rhizome), and a cluster of shield-
like discs, each of which carries a circle of sporanges that open by
longitudinal slits to set free the spores which are attached to it in two pairs
of elastic filaments (shown in Fig. 291, F, G), elaters; these are at first coiled
up around the spore in the manner represented at G, but on their liberation
they extend themselves as shown at F. The slightest moisture will close
them up again, and their purpose having been served in the distribution of
the spores, they are no longer required. If a number of spores be spread out
on a glass-slip under the microscope and, while watching, a bystander
breathes upon them, they immediately respond, are set in motion,
presenting a curious appearance, but as soon as the hydroscopic effect has
passed off they return to their previous condition. These spores can be
mounted in a cell with a movable cover, and made to exhibit the same effect
over and over again.
Fig. 309.—Equisetum giganticum.
a. Fragment of stem showing mode of branching out; b. Cone or spike of
fructification; c. Scale detached from cone; d. Spore with elastic filaments; e.
Vertical section of stem; f. Transverse section showing hexagonal cells.
The vascular tissue of the Equisetaceæ (Fig. 309, e, f) shows them to be of a
higher grade than the ferns. More recently discovered Horse-tails, of Brazil,
grow to a gigantic size, but even these are comparatively small when
compared with the Calamites, and other fossil Equisetaceæ of the coal
branches (the real stem being a horizontal rhizome), and a cluster of shield-
like discs, each of which carries a circle of sporanges that open by
longitudinal slits to set free the spores which are attached to it in two pairs
of elastic filaments (shown in Fig. 291, F, G), elaters; these are at first coiled
up around the spore in the manner represented at G, but on their liberation
they extend themselves as shown at F. The slightest moisture will close
them up again, and their purpose having been served in the distribution of
the spores, they are no longer required. If a number of spores be spread out
on a glass-slip under the microscope and, while watching, a bystander
breathes upon them, they immediately respond, are set in motion,
presenting a curious appearance, but as soon as the hydroscopic effect has
passed off they return to their previous condition. These spores can be
mounted in a cell with a movable cover, and made to exhibit the same effect
over and over again.
Fig. 309.—Equisetum giganticum.
a. Fragment of stem showing mode of branching out; b. Cone or spike of
fructification; c. Scale detached from cone; d. Spore with elastic filaments; e.
Vertical section of stem; f. Transverse section showing hexagonal cells.
The vascular tissue of the Equisetaceæ (Fig. 309, e, f) shows them to be of a
higher grade than the ferns. More recently discovered Horse-tails, of Brazil,
grow to a gigantic size, but even these are comparatively small when
compared with the Calamites, and other fossil Equisetaceæ of the coal
Page 525
measures and new red sandstone. They all require a calcareous flinty soil
for growth. A spring water-course making its way to the sea, as in the
Chines of the Isle of Wight, is very favourable, the author having gathered
them more than once in Bramble Chine.
Nearly allied to ferns is a little group of small aquatic plants, the
Rhizocarpeæ (pepperworts), which either float on the water or creep along
shallow bottoms. These are chiefly curious from having two kinds of spores
produced from separate sporanges; smaller and larger “microspores”
undergoing progressive sub-division without the formation of a distinct
prothallium; each cell giving origin to an antherozoid, a generative process
said to belong exclusively to flowering plants, corresponding indeed to the
pollen grains of higher plants.
Structure of Phanerogamiæ or Flowering Plants.
The two great divisions of the vegetable kingdom are known as
Cryptogamia and Phanerogamia. It does not follow, however, that there is
any abrupt break between the two, as will appear from the context.
Although it is customary to speak of the flowering plants as a higher grade
of life, yet there is an intermediary class of Phanerogamiæ in which the
conspicuous parts of the generative system partake of a condition closely
resembling those of the higher Cryptogamiæ, observed in Gymnosperms,
Coniferæ, and Cycadæ. So it may be said the distinctive character of the
former is that of reproduction by seeds rather than flowers. The progress of
botanical science during the latter half of the Victorian reign has been quite
as remarkable as that of histology; while the comparative physiology and
morphology of plants have perhaps advanced even more rapidly because
the ground was newer. The consequence is that the specialisation of
botanical science has been brought about con-currently with a more
comprehensive nomenclature. The chief cause in this instance of modern
specialisation is utility. “If we look at the great groups of plants from a
broad point of view, it will be seen that the fungi and the phanerogams
occupy public attention on other grounds than do the algæ, mosses and
ferns. Algæ are especially a physiologist’s group, employed in questions on
nutrition, reproduction, and cell division and growth. The Bryophyta and
for growth. A spring water-course making its way to the sea, as in the
Chines of the Isle of Wight, is very favourable, the author having gathered
them more than once in Bramble Chine.
Nearly allied to ferns is a little group of small aquatic plants, the
Rhizocarpeæ (pepperworts), which either float on the water or creep along
shallow bottoms. These are chiefly curious from having two kinds of spores
produced from separate sporanges; smaller and larger “microspores”
undergoing progressive sub-division without the formation of a distinct
prothallium; each cell giving origin to an antherozoid, a generative process
said to belong exclusively to flowering plants, corresponding indeed to the
pollen grains of higher plants.
Structure of Phanerogamiæ or Flowering Plants.
The two great divisions of the vegetable kingdom are known as
Cryptogamia and Phanerogamia. It does not follow, however, that there is
any abrupt break between the two, as will appear from the context.
Although it is customary to speak of the flowering plants as a higher grade
of life, yet there is an intermediary class of Phanerogamiæ in which the
conspicuous parts of the generative system partake of a condition closely
resembling those of the higher Cryptogamiæ, observed in Gymnosperms,
Coniferæ, and Cycadæ. So it may be said the distinctive character of the
former is that of reproduction by seeds rather than flowers. The progress of
botanical science during the latter half of the Victorian reign has been quite
as remarkable as that of histology; while the comparative physiology and
morphology of plants have perhaps advanced even more rapidly because
the ground was newer. The consequence is that the specialisation of
botanical science has been brought about con-currently with a more
comprehensive nomenclature. The chief cause in this instance of modern
specialisation is utility. “If we look at the great groups of plants from a
broad point of view, it will be seen that the fungi and the phanerogams
occupy public attention on other grounds than do the algæ, mosses and
ferns. Algæ are especially a physiologist’s group, employed in questions on
nutrition, reproduction, and cell division and growth. The Bryophyta and
Page 526
Pteridophyta, are, on the other hand, the domain of the morphologist
concerned with such questions as the alternations of generations and the
evolution of the higher plants.
“Fungi and phanerogams, while equally or even more employed by
specialists in morphology and physiology, appeal widely to general interest,
and evidently so on the ground of utility. Without saying that this enhances
the importance of either group, it certainly attracts scientific attention to
them. However, the histology of the minute cell, in addition to its
importance from an academical point of view, has a special interest for the
microscopist.”
It would be impossible to find anything more remarkable in histology than
the detailed agreement in the structure and behaviour of the nucleus in the
higher plants and the higher animals, an agreement which is conspicuously
manifest in those special divisions which take place during the maturation
of the sexual cells.
So with regard to the question of “alternation of generations.” We have
known since the important discoveries of Hofmeister that the development
of a large part of the vegetable kingdom involves a regular alternation of
two distinct generations, the one which is sexual being constantly
succeeded, so far as the normal cycle is concerned, by the other which is
asexual. This alternation is most marked in the mosses and ferns. In the
Bryophyta the ordinary moss or liverwort plant is the sexual generation of
the ovum, which, when fertilised, gives rise to the moss-fruit, and
represents the asexual stage. The latter is once more seen to form spores
from which the sexual plant is again developed.
In the Pteridophyta the alternation is equally regular, but the relative
development of the two generations is totally different, the sexual form
being the insignificant prothallus, while the whole fern-plant, as we
ordinarily know it, is the asexual generation.
The thallus of some of the lower Bryophyta is quite comparable with the
prothallus of a fern, so as regards the sexual generation there is no difficulty
in seeing the relation of the two classes; but when we come to the asexual
generation or sporophyte the case is totally different. There is no
concerned with such questions as the alternations of generations and the
evolution of the higher plants.
“Fungi and phanerogams, while equally or even more employed by
specialists in morphology and physiology, appeal widely to general interest,
and evidently so on the ground of utility. Without saying that this enhances
the importance of either group, it certainly attracts scientific attention to
them. However, the histology of the minute cell, in addition to its
importance from an academical point of view, has a special interest for the
microscopist.”
It would be impossible to find anything more remarkable in histology than
the detailed agreement in the structure and behaviour of the nucleus in the
higher plants and the higher animals, an agreement which is conspicuously
manifest in those special divisions which take place during the maturation
of the sexual cells.
So with regard to the question of “alternation of generations.” We have
known since the important discoveries of Hofmeister that the development
of a large part of the vegetable kingdom involves a regular alternation of
two distinct generations, the one which is sexual being constantly
succeeded, so far as the normal cycle is concerned, by the other which is
asexual. This alternation is most marked in the mosses and ferns. In the
Bryophyta the ordinary moss or liverwort plant is the sexual generation of
the ovum, which, when fertilised, gives rise to the moss-fruit, and
represents the asexual stage. The latter is once more seen to form spores
from which the sexual plant is again developed.
In the Pteridophyta the alternation is equally regular, but the relative
development of the two generations is totally different, the sexual form
being the insignificant prothallus, while the whole fern-plant, as we
ordinarily know it, is the asexual generation.
The thallus of some of the lower Bryophyta is quite comparable with the
prothallus of a fern, so as regards the sexual generation there is no difficulty
in seeing the relation of the two classes; but when we come to the asexual
generation or sporophyte the case is totally different. There is no
Page 527
appreciable resemblance between the fruit of any of the Bryophyta and the
plant of any vascular Cryptogam.
“It is now known that in the higher plants a remarkable numerical change
takes place in the constituents of the nucleus of the cell shortly before
fertilisation. In angiospermous plants a reduction of the chromosomes
occurs shortly before differentiation of the sexual cells. Thus, in the case of
the lily, fertilisation is not the simple fusion of nuclear bodies. These
spheres are seen to fuse in pairs, and then by position to determine the plane
of first cleavage of the ovum; agreeing, in fact, closely with what is
observed to take place in the animal kingdom.”
In the higher grades of plants it will be evident that the several tissues that
compose their bodies are not found in the root, stem, and leaf without
definite order and purpose, but that they are grouped into systems for the
performance of different kinds of work. In all flowering plants at least three
different systems may be clearly distinguished. These are the epidermal or
boundary tissue system, the fundamental or ground tissue system, and the
fibro-vascular or conducting system. All three systems of tissue originate
from meristem cells, located at the growing point of the stem and root.
Although these systems characterise the higher types of plants, the
elementary tissues (represented in Plate XIII. and in other figures) enter
alike into the several component parts of nearly all plants. The stem, the
branch, and the root, are alike constituted of an outer coating which affords
a mechanical support, and once formed takes no further share in the
economy of the plant, excepting that of assisting to convey fluid from the
roots to the branches and leaves, an action more of a capillary nature than
vital. The nourishment of the plant is brought about by other material
structures, as the pith, the cortex, the cambium, and so forth, all of which
greatly assist in the formative process. The woody portion of the plants is
especially concerned in furnishing support to the softer pulpy textures,
while the tissues of leaves and flowers are chiefly composed of cells
compactly held together by protoplasmic or albuminoid matter. Water, of
course, enters largely into the constituents of all plants. Beneath the
epidermis is another layer of importance, the parenchymatous, which
becomes more or less solid with the growth of the pith and cellular wall. In
plant of any vascular Cryptogam.
“It is now known that in the higher plants a remarkable numerical change
takes place in the constituents of the nucleus of the cell shortly before
fertilisation. In angiospermous plants a reduction of the chromosomes
occurs shortly before differentiation of the sexual cells. Thus, in the case of
the lily, fertilisation is not the simple fusion of nuclear bodies. These
spheres are seen to fuse in pairs, and then by position to determine the plane
of first cleavage of the ovum; agreeing, in fact, closely with what is
observed to take place in the animal kingdom.”
In the higher grades of plants it will be evident that the several tissues that
compose their bodies are not found in the root, stem, and leaf without
definite order and purpose, but that they are grouped into systems for the
performance of different kinds of work. In all flowering plants at least three
different systems may be clearly distinguished. These are the epidermal or
boundary tissue system, the fundamental or ground tissue system, and the
fibro-vascular or conducting system. All three systems of tissue originate
from meristem cells, located at the growing point of the stem and root.
Although these systems characterise the higher types of plants, the
elementary tissues (represented in Plate XIII. and in other figures) enter
alike into the several component parts of nearly all plants. The stem, the
branch, and the root, are alike constituted of an outer coating which affords
a mechanical support, and once formed takes no further share in the
economy of the plant, excepting that of assisting to convey fluid from the
roots to the branches and leaves, an action more of a capillary nature than
vital. The nourishment of the plant is brought about by other material
structures, as the pith, the cortex, the cambium, and so forth, all of which
greatly assist in the formative process. The woody portion of the plants is
especially concerned in furnishing support to the softer pulpy textures,
while the tissues of leaves and flowers are chiefly composed of cells
compactly held together by protoplasmic or albuminoid matter. Water, of
course, enters largely into the constituents of all plants. Beneath the
epidermis is another layer of importance, the parenchymatous, which
becomes more or less solid with the growth of the pith and cellular wall. In
Page 528
the pulpy substance of some leaves the epidermis presents a thin lamina of
palisade-tissue, the bulk of the mesophyll consisting of spongy parenchyma
or sclerenchymatous fibres (seen in Fig. 310), which also serve to show the
disposition of the several layers about to be brought under notice.
Development of the Tissue Systems.—In the growing plant the embryonic
cells soon become differentiated into three primary meristem layers, known
as dermatogen, periblem, and phloem, from which are developed
respectively the primary cortex, epidermis, and the stele or vascular
cylinder. The dermatogen forms the outermost layer of cells at the growing
point, and when present always develops into true epidermal tissue. In
stems the dermatogen is always single-layered, while in roots it consists of
several layers and develops a many-layered epidermis.
Fig. 310.—Section of Leaf of Piper.
c. Cortex; ep. Epidermis; pal. Palisade-tissue; scl f. Sclerenchymatous fibres of
pericycle; o. Oil gland.
The periblem occurs immediately beneath the dermatogen, forming a
hollow cylinder of tissue, which surrounds the phloem. From the periblem
is developed the fundamental tissue of the primary cortex. When no
dermatogen is present in the growing-point (stems of vascular cryptogams)
palisade-tissue, the bulk of the mesophyll consisting of spongy parenchyma
or sclerenchymatous fibres (seen in Fig. 310), which also serve to show the
disposition of the several layers about to be brought under notice.
Development of the Tissue Systems.—In the growing plant the embryonic
cells soon become differentiated into three primary meristem layers, known
as dermatogen, periblem, and phloem, from which are developed
respectively the primary cortex, epidermis, and the stele or vascular
cylinder. The dermatogen forms the outermost layer of cells at the growing
point, and when present always develops into true epidermal tissue. In
stems the dermatogen is always single-layered, while in roots it consists of
several layers and develops a many-layered epidermis.
Fig. 310.—Section of Leaf of Piper.
c. Cortex; ep. Epidermis; pal. Palisade-tissue; scl f. Sclerenchymatous fibres of
pericycle; o. Oil gland.
The periblem occurs immediately beneath the dermatogen, forming a
hollow cylinder of tissue, which surrounds the phloem. From the periblem
is developed the fundamental tissue of the primary cortex. When no
dermatogen is present in the growing-point (stems of vascular cryptogams)
Page 529
the external layer of the periblem develops cells which perform epidermal
functions. The phloem occupies the centre of the growing-point, and
consists of a solid mass of somewhat elongated cells. From the phloem are
developed the fibro-vascular and fundamental tissues of the vascular-
cylinder or stele.
PLATE XIII.
ELEMENTARY PLANT TISSUES.
Epidermal or Boundary Tissue System.—This system constitutes the
external covering of the plant, and is commonly called the epidermis. It
includes, besides the ordinary epidermal cells, the guard-cells of the
stomata and water pores, the plant hairs or trichomes, and the epidermal or
external glands. The epidermal tissues are chiefly protective in function,
functions. The phloem occupies the centre of the growing-point, and
consists of a solid mass of somewhat elongated cells. From the phloem are
developed the fibro-vascular and fundamental tissues of the vascular-
cylinder or stele.
PLATE XIII.
ELEMENTARY PLANT TISSUES.
Epidermal or Boundary Tissue System.—This system constitutes the
external covering of the plant, and is commonly called the epidermis. It
includes, besides the ordinary epidermal cells, the guard-cells of the
stomata and water pores, the plant hairs or trichomes, and the epidermal or
external glands. The epidermal tissues are chiefly protective in function,
Page 530
serving to prevent excessive evaporation from the interior tissues of the
plant.
Fig. 311.
a. Epidermis, reticulated ducts, and conjunctive palisade cells; b. Vertical section
of alder root, woody layer, and boundary ducts.
In stems the external layer of cells, whatever its origin, is known as the
epidermis, while in roots it is called the epiblema. The epidermis usually
consists of a single layer of cells, but in some cases it is two or three-
layered, as in the leaves of figs and begonias.
In land plants the epidermis is usually strongly cutinised, while in
submerged plants it is never cutinised. The epidermis of land plants is also
often waxy, the wax occurring on the surface as minute grains, rods or
flakes, constituting the so-called bloom of leaves and fruits, and giving to
them their glaucous appearance. Chlorophyll bodies are usually absent from
the ordinary epidermal cells of land plants, while they commonly occur in
the epidermal cells of aquatic plants.
Ordinary epidermal cells are usually thin-walled and transparent, and
contain a nucleus and colourless watery protoplasm, but are destitute of
both chlorophyll-bodies and starch-grains.
The external layers of the outer walls constitute the cuticle of the plant,
while the internal layers and the radial and inner walls are composed of
cellulose. The cells of the epidermis are always very compactly arranged,
plant.
Fig. 311.
a. Epidermis, reticulated ducts, and conjunctive palisade cells; b. Vertical section
of alder root, woody layer, and boundary ducts.
In stems the external layer of cells, whatever its origin, is known as the
epidermis, while in roots it is called the epiblema. The epidermis usually
consists of a single layer of cells, but in some cases it is two or three-
layered, as in the leaves of figs and begonias.
In land plants the epidermis is usually strongly cutinised, while in
submerged plants it is never cutinised. The epidermis of land plants is also
often waxy, the wax occurring on the surface as minute grains, rods or
flakes, constituting the so-called bloom of leaves and fruits, and giving to
them their glaucous appearance. Chlorophyll bodies are usually absent from
the ordinary epidermal cells of land plants, while they commonly occur in
the epidermal cells of aquatic plants.
Ordinary epidermal cells are usually thin-walled and transparent, and
contain a nucleus and colourless watery protoplasm, but are destitute of
both chlorophyll-bodies and starch-grains.
The external layers of the outer walls constitute the cuticle of the plant,
while the internal layers and the radial and inner walls are composed of
cellulose. The cells of the epidermis are always very compactly arranged,
Page 531
having their walls so closely adherent that the intercellular spaces are
entirely obliterated except at the stomata and water-pores.
Fig. 312.
1. Vertical section of leaf of Iris germanica; a, a. Elongated cells of the epiderm; b.
Stomata cut through longitudinally; c, c. Green cells of the parenchyma; d, d.
Colourless tissue of the interior of the leaf. 2. Portion of leaf torn from its surface;
a. Elongated cells of the cuticle; b. Cells of the stomata; c. Cells of the
parenchyma; d. Limiting wall of the epidermic cell; e. Lacunæ or openings in the
parenchyma corresponding to the stomata.
There are exceptions to this rule, as, for example, in Cinchona calisaya,
which shows no trace of epidermis, this being replaced by a corky layer of
tubular cells. Where this occurs in a plant to any extent, the whole of the
outer tissues are displaced, and the bark consists exclusively of phloem
tissues. This, although of constant occurrence in C. calisaya, is not so
common in other species, as C. succirubia, the middle structure of which
consists of parenchyma in which appear more or less numerous isolated
store-cells, and when these are absent there is a formation of rhytidoma and
displacement of the tissues containing the store-cells and ducts. The
chlorophyll of C. succirubia is very marked, and its spectrum presents
seven distinct absorption bands.
The epidermal system of plants in general includes other tissues than those
already named, as the guard-cells of the stomata, the water-pores, plant-
hairs or trichomes, and the external or epidermal glands, all of which are
but modifications of ordinary epidermal tissue.
entirely obliterated except at the stomata and water-pores.
Fig. 312.
1. Vertical section of leaf of Iris germanica; a, a. Elongated cells of the epiderm; b.
Stomata cut through longitudinally; c, c. Green cells of the parenchyma; d, d.
Colourless tissue of the interior of the leaf. 2. Portion of leaf torn from its surface;
a. Elongated cells of the cuticle; b. Cells of the stomata; c. Cells of the
parenchyma; d. Limiting wall of the epidermic cell; e. Lacunæ or openings in the
parenchyma corresponding to the stomata.
There are exceptions to this rule, as, for example, in Cinchona calisaya,
which shows no trace of epidermis, this being replaced by a corky layer of
tubular cells. Where this occurs in a plant to any extent, the whole of the
outer tissues are displaced, and the bark consists exclusively of phloem
tissues. This, although of constant occurrence in C. calisaya, is not so
common in other species, as C. succirubia, the middle structure of which
consists of parenchyma in which appear more or less numerous isolated
store-cells, and when these are absent there is a formation of rhytidoma and
displacement of the tissues containing the store-cells and ducts. The
chlorophyll of C. succirubia is very marked, and its spectrum presents
seven distinct absorption bands.
The epidermal system of plants in general includes other tissues than those
already named, as the guard-cells of the stomata, the water-pores, plant-
hairs or trichomes, and the external or epidermal glands, all of which are
but modifications of ordinary epidermal tissue.
Page 532
The Stomata or Breathing Pores are apertures in the epidermal which lie
over large intercellular spaces (Fig 312, 2, b). These are usually bordered by
two modified epidermal cells, called guard-cells. Stomata are formed in the
following manner: A young epidermal cell divides into two equal portions
by the formation of a septum across its middle, each half developing into a
guard-cell; the septum now splits lengthwise and separates the guard-cells,
leaving an aperture or stoma between them.
In the higher plants the guard-cells of the stomata are crescent-shaped and
occur in pairs, the concave sides of the cells facing each other with the
aperture between, while in mosses the stomata possesses but a single
annular guard-cell which surrounds the aperture. The guard-cells of stomata
usually contain chlorophyll-bodies in addition to the ordinary protoplasm.
They have the power of increasing or diminishing the size of the aperture
under the influence of light and moisture, thus regulating the amount of
evaporation from the internal tissues of the plant.
Water Pores or Water Stomata are apertures in the epidermis, similar in
structure to ordinary stomata, but differ from them both in function and
distribution. Water-pores excrete water in the form of drops, and have their
guard-cells fixed and immovable. They always occur at the ends of vasal
bundles, and are found on the margin and at the apex of leaves.
Plant Hairs or Trichomes are modified epidermal cells prolonged
externally, and may be either unicellular or multicellular. Each hair consists
of a basal portion, or foot, which is embedded among the ordinary
epidermal cells, and an apical portion or body, which is prolonged
externally. Ordinary epidermal hairs are usually thin-walled, the inner
layers of the wall being composed of cellulose, while the outer layer is
more or less strongly cutinised. The walls may become hardened by
deposits of lime-salts or silica. Sometimes the cells become glandular and
secrete oily, resinous, or irritating matters, as in stinging-nettle hairs (Plate
XIII., No. 19), when they are known as glandular hairs. The development of
resin-passages may be observed in transverse sections of the stem of the ivy
(Hedera helix) cut from a young succulent stem, and mounted in glycerine.
The resin is seen scattered through the cortex and pith, and in the soft bast
over large intercellular spaces (Fig 312, 2, b). These are usually bordered by
two modified epidermal cells, called guard-cells. Stomata are formed in the
following manner: A young epidermal cell divides into two equal portions
by the formation of a septum across its middle, each half developing into a
guard-cell; the septum now splits lengthwise and separates the guard-cells,
leaving an aperture or stoma between them.
In the higher plants the guard-cells of the stomata are crescent-shaped and
occur in pairs, the concave sides of the cells facing each other with the
aperture between, while in mosses the stomata possesses but a single
annular guard-cell which surrounds the aperture. The guard-cells of stomata
usually contain chlorophyll-bodies in addition to the ordinary protoplasm.
They have the power of increasing or diminishing the size of the aperture
under the influence of light and moisture, thus regulating the amount of
evaporation from the internal tissues of the plant.
Water Pores or Water Stomata are apertures in the epidermis, similar in
structure to ordinary stomata, but differ from them both in function and
distribution. Water-pores excrete water in the form of drops, and have their
guard-cells fixed and immovable. They always occur at the ends of vasal
bundles, and are found on the margin and at the apex of leaves.
Plant Hairs or Trichomes are modified epidermal cells prolonged
externally, and may be either unicellular or multicellular. Each hair consists
of a basal portion, or foot, which is embedded among the ordinary
epidermal cells, and an apical portion or body, which is prolonged
externally. Ordinary epidermal hairs are usually thin-walled, the inner
layers of the wall being composed of cellulose, while the outer layer is
more or less strongly cutinised. The walls may become hardened by
deposits of lime-salts or silica. Sometimes the cells become glandular and
secrete oily, resinous, or irritating matters, as in stinging-nettle hairs (Plate
XIII., No. 19), when they are known as glandular hairs. The development of
resin-passages may be observed in transverse sections of the stem of the ivy
(Hedera helix) cut from a young succulent stem, and mounted in glycerine.
The resin is seen scattered through the cortex and pith, and in the soft bast
Page 533
which lies outside the cambium in various stages of development, starting
from a group of four cells without intercellular spaces.
Root hairs spring from the epiblema and are never cutinised, but are
frequently more or less mucilaginous. The root-hairs are the principal
absorbing organs of the plant, and are confined to the younger roots,
occurring just above their tips. Root-hairs are never present in aquatic
plants, and are absent from the roots of certain of the Coniferæ. It is a
curious fact with regard to bell-heather growing in higher latitudes, that the
plants possess a peculiar root structure as a protection against droughts. In
most of them the sustentation of life depends upon the formation of a
number of long thin filaments on their roots resembling root-hairs, which
penetrate the root, forming nodular masses within it. These filaments belong
to a fungus entirely parasitic to the root, and yet different from a common
parasite, inasmuch as the plant in this way obtains so much of its
nourishment, and when the fungus is not present, or is removed, the plant
can no longer live on a peaty soil. The leaf-blade of the coarse moorland
grass Nardus is likewise endowed with a singular property—that of rolling
up cylindrically and spreading out again to adapt itself to the dry and wet
weather of the moorlands of Scotland.
Fig. 313.
a. Section of the testa of Gourd Seed, showing communicating cells filled with
colouring matter; b. Section of stem of Clematis, three pores separated and more
highly magnified; c. Transverse section of same, showing medullary rays.
Fundamental or Ground Tissue System.—This system constitutes the
groundwork of plants, and is the system through which the vasal bundles
are distributed. The fundamental tissues are composed largely, though not
wholly, of parenchyma, and are chiefly concerned in the metabolic work of
plant life.
from a group of four cells without intercellular spaces.
Root hairs spring from the epiblema and are never cutinised, but are
frequently more or less mucilaginous. The root-hairs are the principal
absorbing organs of the plant, and are confined to the younger roots,
occurring just above their tips. Root-hairs are never present in aquatic
plants, and are absent from the roots of certain of the Coniferæ. It is a
curious fact with regard to bell-heather growing in higher latitudes, that the
plants possess a peculiar root structure as a protection against droughts. In
most of them the sustentation of life depends upon the formation of a
number of long thin filaments on their roots resembling root-hairs, which
penetrate the root, forming nodular masses within it. These filaments belong
to a fungus entirely parasitic to the root, and yet different from a common
parasite, inasmuch as the plant in this way obtains so much of its
nourishment, and when the fungus is not present, or is removed, the plant
can no longer live on a peaty soil. The leaf-blade of the coarse moorland
grass Nardus is likewise endowed with a singular property—that of rolling
up cylindrically and spreading out again to adapt itself to the dry and wet
weather of the moorlands of Scotland.
Fig. 313.
a. Section of the testa of Gourd Seed, showing communicating cells filled with
colouring matter; b. Section of stem of Clematis, three pores separated and more
highly magnified; c. Transverse section of same, showing medullary rays.
Fundamental or Ground Tissue System.—This system constitutes the
groundwork of plants, and is the system through which the vasal bundles
are distributed. The fundamental tissues are composed largely, though not
wholly, of parenchyma, and are chiefly concerned in the metabolic work of
plant life.
Page 534
Ground tissue includes, besides ordinary parenchyma, collenchyma,
selerenchymatous parenchyma, fibrous tissue, cork, laticiferous and
glandular tissues. To the fundamental system also belongs the chlorophyll
cells of leaves, the thin-walled cells of the pith and medullary rays, the cells
of the cortex of stems and roots, and most of the soft cellular tissues in all
plants.
The lower plants consist almost entirely of fundamental tissue. In the
herbaceous forms of the higher plants the ground tissues largely
predominate, while in woody plants they are present in much smaller
proportion, the vascular tissues being the most abundant. In aquatic plants
generally, the fundamental tissues constitute the principal system.
The hypoderma occurs immediately beneath the epidermis, and consists of
several layers of cells. A collenchymatous hypoderma is found in the stems
and petioles of most herbaceous dicotyls, and frequently occurs next the
mid-rib of leaves, where it forms a strengthening tissue. A
sclerenchymatous hypoderma occurs either as a continuous layer beneath
the epidermis, as in the stems of some ferns, Pteris aquilina, and in leaves
of the pine; or it may form numerous isolated strands beneath the epidermis,
as in the stems of horsetails and in certain Umbelliferæ.
Fig. 314.
selerenchymatous parenchyma, fibrous tissue, cork, laticiferous and
glandular tissues. To the fundamental system also belongs the chlorophyll
cells of leaves, the thin-walled cells of the pith and medullary rays, the cells
of the cortex of stems and roots, and most of the soft cellular tissues in all
plants.
The lower plants consist almost entirely of fundamental tissue. In the
herbaceous forms of the higher plants the ground tissues largely
predominate, while in woody plants they are present in much smaller
proportion, the vascular tissues being the most abundant. In aquatic plants
generally, the fundamental tissues constitute the principal system.
The hypoderma occurs immediately beneath the epidermis, and consists of
several layers of cells. A collenchymatous hypoderma is found in the stems
and petioles of most herbaceous dicotyls, and frequently occurs next the
mid-rib of leaves, where it forms a strengthening tissue. A
sclerenchymatous hypoderma occurs either as a continuous layer beneath
the epidermis, as in the stems of some ferns, Pteris aquilina, and in leaves
of the pine; or it may form numerous isolated strands beneath the epidermis,
as in the stems of horsetails and in certain Umbelliferæ.
Fig. 314.
Page 535
a. Tangential section of Taxus baccata (Yew), showing the woody fibre; b. Vertical
section of same, spiral fibres, and ducts; c. Vertical section of Elm, showing ducts
and dotted cells.
The endodermis is the innermost layer of the extra-stelar fundamental
tissues, and always abuts on the stele or steles. In monocotyls it marks the
boundary between the cortex and the central cylinder, and it is sometimes
spoken of as the nucleus sheath.
In stems the endodermal cells are usually thin-walled and unlignified,
having a suberous thickening band extending round the upper, lower and
lateral surfaces, which in cross-section appears as a black dot on the radial
wall (Fig. 314, c.)
According to its position in the stele, the conjunctive tissue is divided into
three principal portions, viz., that portion which invests the vasal bundles,
the pericycle; that portion which lies between the bundles of the stele, the
interfascicular conjunctive tissue; and that which occupies the centre of the
stele, the medullary conjunctive tissue. The pericycle, formerly called the
pericambium, is the outermost layer of the conjunctive tissue of the stele.
The bundle-sheath of the young stem is more easily recognised than in the
older stem. It is, in fact, a continuous layer of cells, whose radial walls have
a characteristic dark spot on each radial wall. The bundle-sheath lies
immediately outside the vascular bundles, curving slightly towards the
centre of the stem in the spaces between the bundles. It is more prominent
in the stem when very young, as the cells are then filled with starch
granules. This layer of cells will be readily seen in sections treated with
iodine.
In dicotyls and gymnosperms the medullary rays consist essentially of
interfascicular ground tissue. The medullary conjunctive tissue occupies the
centre of the stele, constituting the so-called pith, and usually consists of
parenchymatous cells, but may contain, in addition, either stone cells,
sclerenchyma fibres, laticiferous or glandular tissues.
The Fibro-vascular or Conducting Tissue System.—This system constitutes
the fibrous framework of the plant, and is the system by means of which
section of same, spiral fibres, and ducts; c. Vertical section of Elm, showing ducts
and dotted cells.
The endodermis is the innermost layer of the extra-stelar fundamental
tissues, and always abuts on the stele or steles. In monocotyls it marks the
boundary between the cortex and the central cylinder, and it is sometimes
spoken of as the nucleus sheath.
In stems the endodermal cells are usually thin-walled and unlignified,
having a suberous thickening band extending round the upper, lower and
lateral surfaces, which in cross-section appears as a black dot on the radial
wall (Fig. 314, c.)
According to its position in the stele, the conjunctive tissue is divided into
three principal portions, viz., that portion which invests the vasal bundles,
the pericycle; that portion which lies between the bundles of the stele, the
interfascicular conjunctive tissue; and that which occupies the centre of the
stele, the medullary conjunctive tissue. The pericycle, formerly called the
pericambium, is the outermost layer of the conjunctive tissue of the stele.
The bundle-sheath of the young stem is more easily recognised than in the
older stem. It is, in fact, a continuous layer of cells, whose radial walls have
a characteristic dark spot on each radial wall. The bundle-sheath lies
immediately outside the vascular bundles, curving slightly towards the
centre of the stem in the spaces between the bundles. It is more prominent
in the stem when very young, as the cells are then filled with starch
granules. This layer of cells will be readily seen in sections treated with
iodine.
In dicotyls and gymnosperms the medullary rays consist essentially of
interfascicular ground tissue. The medullary conjunctive tissue occupies the
centre of the stele, constituting the so-called pith, and usually consists of
parenchymatous cells, but may contain, in addition, either stone cells,
sclerenchyma fibres, laticiferous or glandular tissues.
The Fibro-vascular or Conducting Tissue System.—This system constitutes
the fibrous framework of the plant, and is the system by means of which
Page 536
fluids are conducted from one part of the plant to another. Its function is
partly to give strength and support, but principally to conduct the crude and
elaborated juices to and from the leaves. It is found only in the higher
plants, constituting the tough and stringy tissues in stems and roots, and the
system of veins in leaves. The fibro-vascular system consists essentially of
vascular tissue (ducts, tracheids, and sieve-tubes), and forms long strands—
the fibro-vascular bundles—which extend vertically through the
fundamental tissues of the plant. The term “fibro-vascular,” as applied to
the conducting system, is not strictly correct, since fibres do not always
accompany the vascular elements, hence this system is often spoken of as
the vascular system, and the bundles as vascular, or more briefly as vasal
bundles.
That the arrangement, and course of the vascular bundles in dicotyledous
stems are connected with those of the leaves is an obvious fact. It may be
seen in sections of Helianthus, but is more markedly shown in plants with
regularly decussate leaves, as Cerastium, Clematis, &c. Still, the
arrangement of the bundles may differ radically from that of the leaves, and
is, to a certain extent, independent of them. This will be noticed in sections
of Iberis amara, where the bundles do not run longitudinally, but in
tangential spirals. These, as Nägeli pointed out, have no direct relation with
the leaves; and he recommends a series of types for investigation, in which
it will be seen how closely the arrangement of the bundles is connected with
the arrangement of the leaves, and the number of bundles entering the stem
from each leaf: Iberis amara, leaves alternate, leaf-trace with one bundle;
Lupinus, leaves alternate, leaf-trace with three bundles; Cerastium, leaves
opposite, leaf-trace with one bundle; Clematis, leaves opposite, leaf-trace
with three bundles; Stachys, leaves opposite, leaf-trace with two bundles.
partly to give strength and support, but principally to conduct the crude and
elaborated juices to and from the leaves. It is found only in the higher
plants, constituting the tough and stringy tissues in stems and roots, and the
system of veins in leaves. The fibro-vascular system consists essentially of
vascular tissue (ducts, tracheids, and sieve-tubes), and forms long strands—
the fibro-vascular bundles—which extend vertically through the
fundamental tissues of the plant. The term “fibro-vascular,” as applied to
the conducting system, is not strictly correct, since fibres do not always
accompany the vascular elements, hence this system is often spoken of as
the vascular system, and the bundles as vascular, or more briefly as vasal
bundles.
That the arrangement, and course of the vascular bundles in dicotyledous
stems are connected with those of the leaves is an obvious fact. It may be
seen in sections of Helianthus, but is more markedly shown in plants with
regularly decussate leaves, as Cerastium, Clematis, &c. Still, the
arrangement of the bundles may differ radically from that of the leaves, and
is, to a certain extent, independent of them. This will be noticed in sections
of Iberis amara, where the bundles do not run longitudinally, but in
tangential spirals. These, as Nägeli pointed out, have no direct relation with
the leaves; and he recommends a series of types for investigation, in which
it will be seen how closely the arrangement of the bundles is connected with
the arrangement of the leaves, and the number of bundles entering the stem
from each leaf: Iberis amara, leaves alternate, leaf-trace with one bundle;
Lupinus, leaves alternate, leaf-trace with three bundles; Cerastium, leaves
opposite, leaf-trace with one bundle; Clematis, leaves opposite, leaf-trace
with three bundles; Stachys, leaves opposite, leaf-trace with two bundles.
Page 537
Fig. 315.
1. Transverse section of the stem of Cedar, showing xylem or wood; 2. Section of
stem of Conifer, the phloem and zones of annual growth; 3. Section of an Ivory
Nut, cells, and radiating pores; 4. Section of the outer or ligneous portion of same,
with radiating cells.
The connection of the leaf and stem will be best seen by cutting
longitudinal sections through a young node of Helianthus, so as to include
the median plane of the leaf, or of both leaves if opposite to each other, as
they often are; steep them in dilute potash for twenty-four hours and mount
in glycerine. A medium power will serve for their examination. The course
of the vascular bundles will appear dark through the more transparent
parenchyma. The continuity of the tissues of the stem and petiole if
followed will be seen to have no definite boundary between the two parts;
the bundles from the petiole pass into the stem, and no bundle of the upper
internode lies in the same vertical plane as that which enters from the
petiole between two successive bundles of the vascular ring.
Every complete vasal bundle consists of xylem or wood and phloem or
bast.
The former consists essentially of trachery tissue (ducts and tracheids), and
may contain in addition both wood fibres and wood parenchyma. The
phloem or bast consists essentially of sieve tissue, and usually contains
some ordinary parenchyma. In angiosperms companion-cells always
1. Transverse section of the stem of Cedar, showing xylem or wood; 2. Section of
stem of Conifer, the phloem and zones of annual growth; 3. Section of an Ivory
Nut, cells, and radiating pores; 4. Section of the outer or ligneous portion of same,
with radiating cells.
The connection of the leaf and stem will be best seen by cutting
longitudinal sections through a young node of Helianthus, so as to include
the median plane of the leaf, or of both leaves if opposite to each other, as
they often are; steep them in dilute potash for twenty-four hours and mount
in glycerine. A medium power will serve for their examination. The course
of the vascular bundles will appear dark through the more transparent
parenchyma. The continuity of the tissues of the stem and petiole if
followed will be seen to have no definite boundary between the two parts;
the bundles from the petiole pass into the stem, and no bundle of the upper
internode lies in the same vertical plane as that which enters from the
petiole between two successive bundles of the vascular ring.
Every complete vasal bundle consists of xylem or wood and phloem or
bast.
The former consists essentially of trachery tissue (ducts and tracheids), and
may contain in addition both wood fibres and wood parenchyma. The
phloem or bast consists essentially of sieve tissue, and usually contains
some ordinary parenchyma. In angiosperms companion-cells always
Page 538
accompany the sieve-tubes in the phloem, while in gymnosperms they are
absent.
According to the relative positions of the xylem and phloem elements, there
are two principal kinds of conjoint bundles—the collateral and the
concentric. Of these again there are three varieties, but the experiments with
leaves bring out parallel facts; that in ordinary stems the staining of the
wood by an ascending coloured liquid is due, not to the passage of the
coloured liquid up the substance of the wood, but to the permeability of its
ducts and such of its pitted cells as are united into regular canals; and the
facts showing this at the same time indicate with tolerable clearness the
process by which wood is formed, for what in these cases is seen to take
place with dye may be fairly presumed to take place with sap.
Taking it, then, as a fact that the vessels and ducts are the channels through
which the sap is distributed, the varying permeability of their walls, and
consequent formation of wood, is due to the exposure of the plant to
intermittent mechanical strains, actual or potential, or both, in this way. If a
trunk, a bough, shoot, or a petiole is bent by a gust of wind, the substance of
its convex side is subject to longitudinal tension, the substance of its
concave side being at the same time compressed. This is the primary
mechanical effect. The secondary is when the tissues of the convex side are
stretched, and also produce lateral compression. In short, the formation of
wood is dependent upon transverse strains, such as are produced in the
aerial parts of upright plants by the action of the wind.
absent.
According to the relative positions of the xylem and phloem elements, there
are two principal kinds of conjoint bundles—the collateral and the
concentric. Of these again there are three varieties, but the experiments with
leaves bring out parallel facts; that in ordinary stems the staining of the
wood by an ascending coloured liquid is due, not to the passage of the
coloured liquid up the substance of the wood, but to the permeability of its
ducts and such of its pitted cells as are united into regular canals; and the
facts showing this at the same time indicate with tolerable clearness the
process by which wood is formed, for what in these cases is seen to take
place with dye may be fairly presumed to take place with sap.
Taking it, then, as a fact that the vessels and ducts are the channels through
which the sap is distributed, the varying permeability of their walls, and
consequent formation of wood, is due to the exposure of the plant to
intermittent mechanical strains, actual or potential, or both, in this way. If a
trunk, a bough, shoot, or a petiole is bent by a gust of wind, the substance of
its convex side is subject to longitudinal tension, the substance of its
concave side being at the same time compressed. This is the primary
mechanical effect. The secondary is when the tissues of the convex side are
stretched, and also produce lateral compression. In short, the formation of
wood is dependent upon transverse strains, such as are produced in the
aerial parts of upright plants by the action of the wind.
Page 539
Fig. 316.—Termination of Vascular System.
1.—Absorbent organ from the leaf of Euphorbia neriifolia. The cluster of fibrous
cells forming one of the terminations of the vascular system is here embedded in a
solid parenchyma.
2.—A structure of analogous kind from the leaf of Ficus elastica. Here the
expanded terminations of the vessels are embedded in the network parenchyma,
the cells of which unite to form envelopes for them.
3.—End view of an absorbent organ from the root of a turnip. It is taken from the
outermost layer of vessels. Its funnel-shaped interior is drawn as it presents itself
when looked at from the outside of this layer, its narrow end being directed
towards the centre of the turnip.
4.—Shows on a larger scale one of these absorbents from the leaf of Panax
Lessonii. In this figure is clearly seen the way in which the cells of the network
parenchyma unite into a closely-fitting case for the spiral cells.
5.—A less-developed absorbent, showing its approximate connection with a duct.
In their simplest forms these structures consist of only two fenestrated cells, with
1.—Absorbent organ from the leaf of Euphorbia neriifolia. The cluster of fibrous
cells forming one of the terminations of the vascular system is here embedded in a
solid parenchyma.
2.—A structure of analogous kind from the leaf of Ficus elastica. Here the
expanded terminations of the vessels are embedded in the network parenchyma,
the cells of which unite to form envelopes for them.
3.—End view of an absorbent organ from the root of a turnip. It is taken from the
outermost layer of vessels. Its funnel-shaped interior is drawn as it presents itself
when looked at from the outside of this layer, its narrow end being directed
towards the centre of the turnip.
4.—Shows on a larger scale one of these absorbents from the leaf of Panax
Lessonii. In this figure is clearly seen the way in which the cells of the network
parenchyma unite into a closely-fitting case for the spiral cells.
5.—A less-developed absorbent, showing its approximate connection with a duct.
In their simplest forms these structures consist of only two fenestrated cells, with
Page 540
their ends bent round so as to meet. Such types occur in the central mass of the
turnip, where the vascular system is relatively imperfect. Besides the
comparatively regular forms of these absorbents, there are forms composed of
amorphous masses of fenestrated cells. It should be added that both the regular and
irregular kinds are very variable in their numbers: in some turnips they are
abundant, and in others scarcely to be found. Possibly their presence depends on
the age of the turnip.
6.—Represents a much more massive absorbent from the same leaf, the
surrounding tissues being omitted.
7.—Similarly represents, without its sheath, an absorbent from the leaf of Clusia
flava.
8.—A longitudinal section through the axis of another such organ, showing its
annuli of reticulated cells when cut through. The cellular tissue which fills the
interior is supposed to be removed.
In concentric bundles one of the elements, either the xylem or the phloem,
occupies the centre, and is more or less surrounded by the other, as seen in
Fig. 310. Meristem tissue is never present, hence concentric bundles are
always closed. They, however, occur in the stems of most ferns, and are
always surrounded by a pericycle and endodermis, and should be regarded
as steles. Concentric bundles with a central phloem occur in the rhizomes of
some monocotyles, as Calamus, Iris, Convallaria, &c.
The Stele, or Vascular Cylinder, is developed from the phloem of the
growing plant, and consists of one or more vasal bundles imbedded in
fundamental tissue, the whole being enclosed by a pericycle and an
endoderm. The typical stele includes all the tissues evolved by the
endodermis, which, however, forms no part of the vascular cylinder itself,
but merely surrounds it. The pericycle is always the outermost layer of the
tissues of the stele, while the endodermis is the innermost layer of the extra-
stelar tissues.
The arboreus type of stem can be best followed by making sections of a
twig of the elm (Ulmus campestris), which will be found to be cylindrical
hirsute, green or brown according to age, the latter colour being due to the
formation of cork. Small brown excrescences are scattered over its surface;
these are termed lenticels. The cork will be seen to lie immediately below
the epidermis, and to consist of cubical cells, with little or no cell contents;
they are arranged in radial rows, without intercellular spaces. The walls of
turnip, where the vascular system is relatively imperfect. Besides the
comparatively regular forms of these absorbents, there are forms composed of
amorphous masses of fenestrated cells. It should be added that both the regular and
irregular kinds are very variable in their numbers: in some turnips they are
abundant, and in others scarcely to be found. Possibly their presence depends on
the age of the turnip.
6.—Represents a much more massive absorbent from the same leaf, the
surrounding tissues being omitted.
7.—Similarly represents, without its sheath, an absorbent from the leaf of Clusia
flava.
8.—A longitudinal section through the axis of another such organ, showing its
annuli of reticulated cells when cut through. The cellular tissue which fills the
interior is supposed to be removed.
In concentric bundles one of the elements, either the xylem or the phloem,
occupies the centre, and is more or less surrounded by the other, as seen in
Fig. 310. Meristem tissue is never present, hence concentric bundles are
always closed. They, however, occur in the stems of most ferns, and are
always surrounded by a pericycle and endodermis, and should be regarded
as steles. Concentric bundles with a central phloem occur in the rhizomes of
some monocotyles, as Calamus, Iris, Convallaria, &c.
The Stele, or Vascular Cylinder, is developed from the phloem of the
growing plant, and consists of one or more vasal bundles imbedded in
fundamental tissue, the whole being enclosed by a pericycle and an
endoderm. The typical stele includes all the tissues evolved by the
endodermis, which, however, forms no part of the vascular cylinder itself,
but merely surrounds it. The pericycle is always the outermost layer of the
tissues of the stele, while the endodermis is the innermost layer of the extra-
stelar tissues.
The arboreus type of stem can be best followed by making sections of a
twig of the elm (Ulmus campestris), which will be found to be cylindrical
hirsute, green or brown according to age, the latter colour being due to the
formation of cork. Small brown excrescences are scattered over its surface;
these are termed lenticels. The cork will be seen to lie immediately below
the epidermis, and to consist of cubical cells, with little or no cell contents;
they are arranged in radial rows, without intercellular spaces. The walls of
Page 541
these cork cells will stain
yellowish-brown with Schultze’s
solution. Treat a thin section with
sulphuric acid and the walls will
swell out and gradually lose their
sharpness of outline, with the
exception of the cuticularised
outer wall of the epidermis and
the cork. This material is
occasionally found developed in
the twigs of the elm, so that it can
be separated as thick radial plates
of tissue.
“By comparing sections of twigs
cut of various ages, the following
information may be gleaned:
Fig. 317.—Vertical section of Sugar-cane Stem That cork cambium, or
showing parachyma and crystalline cells, × 200 phellogen, appears as a layer of
diameters. cortical cells below the
epidermis, and that these divide
parallel to the surface of the stem. The result of successive divisions in this
direction is the formation of secondary tissue, which develops externally as
cork, internally as phelloderm. The true cork cambium consists of only a
single cell in each radial row, from which, by successive division, all these
secondary tissues are derived—i.e., cambium of vascular bundles. As stems
grow older, layers of cork appear successively further and further from the
external surface; not only the cortex, but also the outer portions of the
phloem are thus cut off from physiological connection with the inner tissue.
The term bark is applied to tissues thus cut off, together with the cork
which forms the physiological boundary. The stem of Vitis affords a good
example of such successive layers of cork.”
yellowish-brown with Schultze’s
solution. Treat a thin section with
sulphuric acid and the walls will
swell out and gradually lose their
sharpness of outline, with the
exception of the cuticularised
outer wall of the epidermis and
the cork. This material is
occasionally found developed in
the twigs of the elm, so that it can
be separated as thick radial plates
of tissue.
“By comparing sections of twigs
cut of various ages, the following
information may be gleaned:
Fig. 317.—Vertical section of Sugar-cane Stem That cork cambium, or
showing parachyma and crystalline cells, × 200 phellogen, appears as a layer of
diameters. cortical cells below the
epidermis, and that these divide
parallel to the surface of the stem. The result of successive divisions in this
direction is the formation of secondary tissue, which develops externally as
cork, internally as phelloderm. The true cork cambium consists of only a
single cell in each radial row, from which, by successive division, all these
secondary tissues are derived—i.e., cambium of vascular bundles. As stems
grow older, layers of cork appear successively further and further from the
external surface; not only the cortex, but also the outer portions of the
phloem are thus cut off from physiological connection with the inner tissue.
The term bark is applied to tissues thus cut off, together with the cork
which forms the physiological boundary. The stem of Vitis affords a good
example of such successive layers of cork.”
Page 542
Fig. 318.
1. Laticiferous Tissue; 2. Vertical section of a Leaf of the India-rubber Tree, with a
central gland; 3. Vertical cast of spiral tubes of Opuntia.
For the study of sieve-tubes take the vegetable marrow, in which they are of
extraordinary size. Cut transverse sections of the stem and stain with eosin,
and mount them in glycerine. The general arrangement will be seen to differ
from that of most other herbaceous plants. Below the epidermis a thick
walled band of sclerenchyma with lignified walls will be seen distinct from
the vascular bundles, which readily take a stain. The vascular bundles are
separate and distinct, and the structure of the bundle is abnormal, there
being in each a separate central mass of xylem, with the phloem masses
lying, the one central, the other in the peripheral side. Between the xylem
and the phloem masses is the cambium layer. The structure being the same
in both will serve for the study of the punctate sieve-plates; these are readily
stained with eosin, as shown in Sach’s text-book.
Laticiferous Tissues (Fig. 318).—In cutting sections of latex care must be
taken to at once transfer them to alcohol so as to prevent the flow of the
latex from the cells, otherwise the laticiferous vessels will be much less
easily traced. The better method is to plunge the root of the dandelion
(Leontodon taraxacum), after cleaning, into alcohol, and there let it remain
until it has become hardened; then cut thin tangential sections from the
phloem, and longitudinal sections through the cambium, and mount them in
potash and glycerine. The laticiferous vessels appear circular in the
1. Laticiferous Tissue; 2. Vertical section of a Leaf of the India-rubber Tree, with a
central gland; 3. Vertical cast of spiral tubes of Opuntia.
For the study of sieve-tubes take the vegetable marrow, in which they are of
extraordinary size. Cut transverse sections of the stem and stain with eosin,
and mount them in glycerine. The general arrangement will be seen to differ
from that of most other herbaceous plants. Below the epidermis a thick
walled band of sclerenchyma with lignified walls will be seen distinct from
the vascular bundles, which readily take a stain. The vascular bundles are
separate and distinct, and the structure of the bundle is abnormal, there
being in each a separate central mass of xylem, with the phloem masses
lying, the one central, the other in the peripheral side. Between the xylem
and the phloem masses is the cambium layer. The structure being the same
in both will serve for the study of the punctate sieve-plates; these are readily
stained with eosin, as shown in Sach’s text-book.
Laticiferous Tissues (Fig. 318).—In cutting sections of latex care must be
taken to at once transfer them to alcohol so as to prevent the flow of the
latex from the cells, otherwise the laticiferous vessels will be much less
easily traced. The better method is to plunge the root of the dandelion
(Leontodon taraxacum), after cleaning, into alcohol, and there let it remain
until it has become hardened; then cut thin tangential sections from the
phloem, and longitudinal sections through the cambium, and mount them in
potash and glycerine. The laticiferous vessels appear circular in the
Page 543
transverse sections with brown contents; these are distributed in groups
round the central xylem. Observe in such sections the presence of sphere
crystals of inulin. These are formed quite irrespective of the cell-walls.
Laticiferous cells are readily seen in the cortex of Euphorbia splendens, cut
just outside the vascular ring. Long tubes will be seen to run through the
cortical parenchyma, with thick cellulose walls and granular contents.
These are the laticiferous cells, the branching of which distinguishes them
from the preceding structure. Included in the granular contents are starch
grains of a peculiar dumb-bell form.
Leaf or Petiole.—The general morphology of leaf tissue is essentially the
same as that of the stem from which it proceeds. In the typical monostotic
stem of Phanerogamæ each leaf receives a portion of the stele or central
cylinder of the stem. Such portion is termed a meristele, and may be either
entire or split up into a number of schizosteles.
The microscopical structure of leaves should be studied in the whole organ,
and by the aid of isolating elements. The whole or portion of a leaf should
be soaked in chloral hydrate solution; this will render it transparent,
whereby the internal structure can be studied as a whole. Sections should be
prepared from fresh leaves, or dried ones softened by soaking in water. Cut
them transversely, both in the direction of the mid-rib and at right angles to
it. This is best effected by placing the material between two pieces of elder
pith or fresh carrot. Sections of the whole are made and transferred to a dish
of water. Leaf sections are easily made for examination by macerating the
leaves in solution of caustic potash varying in strength from one to five per
cent. The epidermis on both sides may be detached, and the elements of the
mesophyll and vascular bundles isolated for separate examination.
Potassium permanganate proves to be a useful reagent. A weak solution
causes the protoplasmic structures to swell up, thus assisting in the
observation of the structure of the chromatophores. This solution may also
be employed as a macerating fluid. Beautiful preparations are obtained in
this way of the sieve-tubes of Vitis.
Special structural peculiarities are to be observed in the leaves of various
plants in which the epidermis consists of more than a single layer of cells
round the central xylem. Observe in such sections the presence of sphere
crystals of inulin. These are formed quite irrespective of the cell-walls.
Laticiferous cells are readily seen in the cortex of Euphorbia splendens, cut
just outside the vascular ring. Long tubes will be seen to run through the
cortical parenchyma, with thick cellulose walls and granular contents.
These are the laticiferous cells, the branching of which distinguishes them
from the preceding structure. Included in the granular contents are starch
grains of a peculiar dumb-bell form.
Leaf or Petiole.—The general morphology of leaf tissue is essentially the
same as that of the stem from which it proceeds. In the typical monostotic
stem of Phanerogamæ each leaf receives a portion of the stele or central
cylinder of the stem. Such portion is termed a meristele, and may be either
entire or split up into a number of schizosteles.
The microscopical structure of leaves should be studied in the whole organ,
and by the aid of isolating elements. The whole or portion of a leaf should
be soaked in chloral hydrate solution; this will render it transparent,
whereby the internal structure can be studied as a whole. Sections should be
prepared from fresh leaves, or dried ones softened by soaking in water. Cut
them transversely, both in the direction of the mid-rib and at right angles to
it. This is best effected by placing the material between two pieces of elder
pith or fresh carrot. Sections of the whole are made and transferred to a dish
of water. Leaf sections are easily made for examination by macerating the
leaves in solution of caustic potash varying in strength from one to five per
cent. The epidermis on both sides may be detached, and the elements of the
mesophyll and vascular bundles isolated for separate examination.
Potassium permanganate proves to be a useful reagent. A weak solution
causes the protoplasmic structures to swell up, thus assisting in the
observation of the structure of the chromatophores. This solution may also
be employed as a macerating fluid. Beautiful preparations are obtained in
this way of the sieve-tubes of Vitis.
Special structural peculiarities are to be observed in the leaves of various
plants in which the epidermis consists of more than a single layer of cells
Page 544
(e.g., the leaves of Ficus, Peperaceæ, Begoniaceæ, &c.), cystoleths in the
cells of the epidermis of Urtica; glandular structure in Ruta, Psorales; the
coriaceous leaves of the Cherry Laurel, and the cylindrical leaves of
Stonecrop (Sedum acre).
Reproductive Organs.—The development of the rudiments of flowers is of
an extremely interesting nature, and the complete flower should be carefully
studied. Median sections are best suited for the purpose. In the large
majority of plants the calyx is developed first, then the corolla, and next the
stamens. Preparations should be made from materials hardened in alcohol,
or first fixed with a strong solution of picric acid and then hardened in
alcohol.
Pollen-grains.—Microspores are found lying free in sections made of the
reproductive organs; these may be transferred to a glycerine fluid and
examined under a high power. They are mostly spherical, with granular
protoplasmic contents, in which with much difficulty two nuclei can be
made out. Mount and examine, as types of the various forms of granules,
the pollen of Helianthus, Althœa, Cucurbita, Ænothera, Orchis, Mimosa,
Tulipa, &c. Mount any of these pollen-grains in a weak solution of cane-
sugar (about five per cent.), examine with a high power, and note the
configuration of their walls with a medium power under polarised light. If
transverse sections be made from very young buds, the development of the
anther and the pollen may be traced. The material should be preserved in
strong alcohol, and the sections treated with equal parts of alcohol and
glycerine, and exposed in a watch-glass that the alcohol may evaporate. By
this method sections may be prepared for illustrating the formation of the
tapetum, special mother-cells, and division of the nucleus.
Starch Granules.—One of the most universally distributed materials found
in plants is starch composed of two substances, granulose, which
constitutes by far the largest part, and a skeleton of farinose. It is only the
former of these that stains blue with iodine solutions; the latter partially
assumes a brownish colour. The structure of starch granules is not of equal
density throughout; the hilum or nuclear portion is most conspicuous,
around which the rest of the material is deposited in layers, indicative of
stratification. The several layers next to the hilum are less dense than those
cells of the epidermis of Urtica; glandular structure in Ruta, Psorales; the
coriaceous leaves of the Cherry Laurel, and the cylindrical leaves of
Stonecrop (Sedum acre).
Reproductive Organs.—The development of the rudiments of flowers is of
an extremely interesting nature, and the complete flower should be carefully
studied. Median sections are best suited for the purpose. In the large
majority of plants the calyx is developed first, then the corolla, and next the
stamens. Preparations should be made from materials hardened in alcohol,
or first fixed with a strong solution of picric acid and then hardened in
alcohol.
Pollen-grains.—Microspores are found lying free in sections made of the
reproductive organs; these may be transferred to a glycerine fluid and
examined under a high power. They are mostly spherical, with granular
protoplasmic contents, in which with much difficulty two nuclei can be
made out. Mount and examine, as types of the various forms of granules,
the pollen of Helianthus, Althœa, Cucurbita, Ænothera, Orchis, Mimosa,
Tulipa, &c. Mount any of these pollen-grains in a weak solution of cane-
sugar (about five per cent.), examine with a high power, and note the
configuration of their walls with a medium power under polarised light. If
transverse sections be made from very young buds, the development of the
anther and the pollen may be traced. The material should be preserved in
strong alcohol, and the sections treated with equal parts of alcohol and
glycerine, and exposed in a watch-glass that the alcohol may evaporate. By
this method sections may be prepared for illustrating the formation of the
tapetum, special mother-cells, and division of the nucleus.
Starch Granules.—One of the most universally distributed materials found
in plants is starch composed of two substances, granulose, which
constitutes by far the largest part, and a skeleton of farinose. It is only the
former of these that stains blue with iodine solutions; the latter partially
assumes a brownish colour. The structure of starch granules is not of equal
density throughout; the hilum or nuclear portion is most conspicuous,
around which the rest of the material is deposited in layers, indicative of
stratification. The several layers next to the hilum are less dense than those
Page 545
farthest from it. The position of the
hilum determines the form of the
grain, a few being rounded, others
oval or elongated. The grain also
contains different proportions of
water; this conveys the appearance of
concentric lines or curves about the
nucleus. The latter is more
conspicuous in the potato starches, as
seen in Plate XIII., Nos. 6-15. Starch
grains, in nearly all cases, are formed
by the agency of proteid bodies,
Fig. 319.—Pollen Grains. either chloroplasts or amyloplasts,
A. Pollen-grain of Clove-pink; B. Poppy; C.
and under the action of sunlight are
Passion-flower (Passiflora cœrulea); D. Cobœa gradually broken up and employed in
scandens. the process of growth. There are
some plants, however, notably the
Compositeæ, in which another carbohydrate, inulin, takes the place of
starch from the first, and is used as a reserve food material. For this reason
we look in vain for starch in the cells of Inula, Taraxacum, &c. From the
whole group of fungi starch is absent; this seems to explain the fact that
chlorophyll, or colouring matter, is rarely met with in the fungi, hence their
inability to utilize, like green plants, carbon-dioxide as food.
hilum determines the form of the
grain, a few being rounded, others
oval or elongated. The grain also
contains different proportions of
water; this conveys the appearance of
concentric lines or curves about the
nucleus. The latter is more
conspicuous in the potato starches, as
seen in Plate XIII., Nos. 6-15. Starch
grains, in nearly all cases, are formed
by the agency of proteid bodies,
Fig. 319.—Pollen Grains. either chloroplasts or amyloplasts,
A. Pollen-grain of Clove-pink; B. Poppy; C.
and under the action of sunlight are
Passion-flower (Passiflora cœrulea); D. Cobœa gradually broken up and employed in
scandens. the process of growth. There are
some plants, however, notably the
Compositeæ, in which another carbohydrate, inulin, takes the place of
starch from the first, and is used as a reserve food material. For this reason
we look in vain for starch in the cells of Inula, Taraxacum, &c. From the
whole group of fungi starch is absent; this seems to explain the fact that
chlorophyll, or colouring matter, is rarely met with in the fungi, hence their
inability to utilize, like green plants, carbon-dioxide as food.
Page 546
Fig. 320.—Swollen Potato Starch, after the application of potassium hydrate.
(Magnified 210 diameters.)
The tissues which most commonly contain starch, or which contain it in
largest quantity, are those of the parenchymatous series, though it
sometimes occurs in the latex of laticiferous tissues, and even in ducts and
tracheids. In the stems of Dicotyledons it occurs chiefly in the parenchyma
of the middle and inner bark, in the medullary ray cells, and in the cells of
the pith. In the roots of these plants it has a similar distribution, being for
the most part confined to the middle or inner bark and the medullary rays,
pith not being present in these organs. In succulent stems and roots, of
course, it also commonly occurs in the xylem tissues of the fibro-vascular
bundles.
(Magnified 210 diameters.)
The tissues which most commonly contain starch, or which contain it in
largest quantity, are those of the parenchymatous series, though it
sometimes occurs in the latex of laticiferous tissues, and even in ducts and
tracheids. In the stems of Dicotyledons it occurs chiefly in the parenchyma
of the middle and inner bark, in the medullary ray cells, and in the cells of
the pith. In the roots of these plants it has a similar distribution, being for
the most part confined to the middle or inner bark and the medullary rays,
pith not being present in these organs. In succulent stems and roots, of
course, it also commonly occurs in the xylem tissues of the fibro-vascular
bundles.
Page 547
A study of the various kinds of starches is important, since this material is
very largely used as an adulterant. Other than microscopical means of
detecting frauds are practically useless; assaying is tedious and expensive,
while the microscope is always available and at hand. The limits of
variation should be studied in starches from the same species of plants; the
variations are not very wide, but in most cases characteristic, so that the
discrimination is at all times an easy task. The reagents required are simply
iodine and dilute potassium hydrate, aided by polarised light.
Fig. 321.
a a a. Granules and cells of cocoa; b b b. Arrowroot, Tous-les-mois; c c c. Tapioca
starch. (Magnified 300 diameters.)
very largely used as an adulterant. Other than microscopical means of
detecting frauds are practically useless; assaying is tedious and expensive,
while the microscope is always available and at hand. The limits of
variation should be studied in starches from the same species of plants; the
variations are not very wide, but in most cases characteristic, so that the
discrimination is at all times an easy task. The reagents required are simply
iodine and dilute potassium hydrate, aided by polarised light.
Fig. 321.
a a a. Granules and cells of cocoa; b b b. Arrowroot, Tous-les-mois; c c c. Tapioca
starch. (Magnified 300 diameters.)
Page 548
The starch grains of the potato are the best to study in the first instance on
account of their large size (Fig. 320).
In arrowroot starch (Fig. 321) the stratification is almost as distinct as in
that of the potato; the grains much resemble each other. Although somewhat
smaller, the grains of arrowroot are more uniform in size. The starches are
much used as an adulterant of drugs and various articles sold as cocoas.
Wheat-starch (Fig. 322) consists of circular flattened grains varying much
in size, the central nucleus and stratification of which are very difficult to
distinguish.
In the smaller starches the hilum becomes more indistinct, and without
stratification, as in rice-starch, the latter being angular in shape. The hilum
in other leguminous plants forms a longitudinal cleft; white rye-starch
exhibits distinct cracks. Compound grains are occasionally met with, as in
the oat. In Plate XIII. will be found small groups of starches taken under the
same medium power for the sake of comparison. In the microscopical
examination of starches first use a 2⁄3-inch or a ½-inch and then a 1⁄6-inch
objective.
account of their large size (Fig. 320).
In arrowroot starch (Fig. 321) the stratification is almost as distinct as in
that of the potato; the grains much resemble each other. Although somewhat
smaller, the grains of arrowroot are more uniform in size. The starches are
much used as an adulterant of drugs and various articles sold as cocoas.
Wheat-starch (Fig. 322) consists of circular flattened grains varying much
in size, the central nucleus and stratification of which are very difficult to
distinguish.
In the smaller starches the hilum becomes more indistinct, and without
stratification, as in rice-starch, the latter being angular in shape. The hilum
in other leguminous plants forms a longitudinal cleft; white rye-starch
exhibits distinct cracks. Compound grains are occasionally met with, as in
the oat. In Plate XIII. will be found small groups of starches taken under the
same medium power for the sake of comparison. In the microscopical
examination of starches first use a 2⁄3-inch or a ½-inch and then a 1⁄6-inch
objective.
Page 549
Fig. 322.
a. Husks of Wheat-starch, swollen by reagents and heat; b. A portion of cellulose;
c. Rice-starch, magnified 420 diameters.
The bran of the husk of wheat when broken by grinding is seen to be
composed of two coats of hexagonal cells, the outer of which is detached by
the roasting process. The hexagonal cell layer is, however, so little altered
as to be perfectly distinguishable under the microscope. Thus even a small
admixture of roasted corn with coffee or chicory can be detected without
much difficulty. As to whether starch granules should be regarded as
crystalline or colloid bodies, a difference of opinion still prevails. There are,
however, reasons for believing that the polarisation effects produced by
starch grains are not due to crystalline structure but to stress or strain, of the
same nature as the polarisation of glass when it is subject to strain. The
a. Husks of Wheat-starch, swollen by reagents and heat; b. A portion of cellulose;
c. Rice-starch, magnified 420 diameters.
The bran of the husk of wheat when broken by grinding is seen to be
composed of two coats of hexagonal cells, the outer of which is detached by
the roasting process. The hexagonal cell layer is, however, so little altered
as to be perfectly distinguishable under the microscope. Thus even a small
admixture of roasted corn with coffee or chicory can be detected without
much difficulty. As to whether starch granules should be regarded as
crystalline or colloid bodies, a difference of opinion still prevails. There are,
however, reasons for believing that the polarisation effects produced by
starch grains are not due to crystalline structure but to stress or strain, of the
same nature as the polarisation of glass when it is subject to strain. The
Page 550
polarising phenomena are precisely such as would be induced in any
transparent solid composed of layers, the inner of which being kept in a
state of stress by the compression exerted by the outer layers. Moreover,
when by use of a swelling reagent, such as caustic potash solution, the outer
wall of the starch is made to expand by the imbibition of water, the
polarisation effects immediately disappear. Were the solid particles of
crystal thus forced apart by water each particle would still exhibit
polarisation phenomena.
Want of space will not permit me to further enlarge upon other micro-
chemical substances that enter into the composition of plants; as, for
example, the oil secreting glands. These when present take the place of
starch. There is, however, one product among the cell contents of plants of
some interest to the microscopist—those extremely fine crystals known as
raphides, composed of calcium-phosphate and oxalate. Mr. Gulliver
insisted upon the value of raphides as characteristic of several families of
plants. Schleiden states that “needle-formed crystals, in bundles of from
twenty to thirty in a cell, are present in almost all plants,” and that so really
practical is the presence or absence of raphides, that by studying them he
has been able to pick out pots of seedling Onagraceæ, which had been
accidentally mixed with pots of other seedlings of the same age, and at that
period of growth when no other botanical character would have been so
readily sufficient.
If we examine a portion of the layers of an onion (Plate XIV., No. 3), or a
thin section of the stem or root of the garden rhubarb (No. 4), we shall find
many cells in which either bundles of needle-shaped crystals or masses of a
stellate form occur, not strictly raphides.
Raphides were first noticed by Malpighi in Opuntia, and subsequently
described by Jurine and Raspail. According to the latter observer, the
needle-shaped or acicular are composed of phosphate, and the stellate of
oxalate of lime. There are others having lime as a basis, in combination
with tartaric, malic, and citric acids, all of which are destroyed by acetic
acid; others are soluble in many of the fluids employed in mounting. These
crystals vary in size from the 1⁄40th of an inch, while others are as small as
the 1⁄1000th. They occur in all parts of the plant; in the stem, bark, leaf, petals,
transparent solid composed of layers, the inner of which being kept in a
state of stress by the compression exerted by the outer layers. Moreover,
when by use of a swelling reagent, such as caustic potash solution, the outer
wall of the starch is made to expand by the imbibition of water, the
polarisation effects immediately disappear. Were the solid particles of
crystal thus forced apart by water each particle would still exhibit
polarisation phenomena.
Want of space will not permit me to further enlarge upon other micro-
chemical substances that enter into the composition of plants; as, for
example, the oil secreting glands. These when present take the place of
starch. There is, however, one product among the cell contents of plants of
some interest to the microscopist—those extremely fine crystals known as
raphides, composed of calcium-phosphate and oxalate. Mr. Gulliver
insisted upon the value of raphides as characteristic of several families of
plants. Schleiden states that “needle-formed crystals, in bundles of from
twenty to thirty in a cell, are present in almost all plants,” and that so really
practical is the presence or absence of raphides, that by studying them he
has been able to pick out pots of seedling Onagraceæ, which had been
accidentally mixed with pots of other seedlings of the same age, and at that
period of growth when no other botanical character would have been so
readily sufficient.
If we examine a portion of the layers of an onion (Plate XIV., No. 3), or a
thin section of the stem or root of the garden rhubarb (No. 4), we shall find
many cells in which either bundles of needle-shaped crystals or masses of a
stellate form occur, not strictly raphides.
Raphides were first noticed by Malpighi in Opuntia, and subsequently
described by Jurine and Raspail. According to the latter observer, the
needle-shaped or acicular are composed of phosphate, and the stellate of
oxalate of lime. There are others having lime as a basis, in combination
with tartaric, malic, and citric acids, all of which are destroyed by acetic
acid; others are soluble in many of the fluids employed in mounting. These
crystals vary in size from the 1⁄40th of an inch, while others are as small as
the 1⁄1000th. They occur in all parts of the plant; in the stem, bark, leaf, petals,
Page 551
fruit, root, and even in the pollen, and occasionally in the interior of cells.
In certain species of aloe, as Aloe verrucosa, we are able to discern small
silky filaments; these are bundles of the acicular form of raphides, and
probably, as in sponges, act as a skeleton support to the internal soft pulpy
mass.
PLATE XIV.
STELLATE AND CRYSTALLINE TISSUE OF PLANTS.
In portions of the cuticle of the medicinal squill (Scilla maritima) large cells
are found full of needle-shaped crystals. These cells, however, do not lie in
the same plane as the smaller cells of the cuticle. In the cuticle of an onion
every cell is occupied either by an octahedral or a prismatic crystal of
calcium oxalate. In some specimens the octahedral form predominates; in
In certain species of aloe, as Aloe verrucosa, we are able to discern small
silky filaments; these are bundles of the acicular form of raphides, and
probably, as in sponges, act as a skeleton support to the internal soft pulpy
mass.
PLATE XIV.
STELLATE AND CRYSTALLINE TISSUE OF PLANTS.
In portions of the cuticle of the medicinal squill (Scilla maritima) large cells
are found full of needle-shaped crystals. These cells, however, do not lie in
the same plane as the smaller cells of the cuticle. In the cuticle of an onion
every cell is occupied either by an octahedral or a prismatic crystal of
calcium oxalate. In some specimens the octahedral form predominates; in
Page 552
others, even from the same plant, the crystals are prismatic and arranged in
a stellate form, as in that of the grass (Pharus cristatus). (Plate XIV., No. 6.)
Raphides of peculiar figure are found in the bark of certain trees. In the
hickory (Carya alba) may be observed masses of flattened prisms having
both extremities pointed. In vertical sections from the stem of Elæagnus
angustifolia, numerous raphides of large size are embedded in the pith, and
also found in the bark of the apple-tree, and in elm seeds, every cell
containing two or more minute crystals.
In the Graminaceæ, especially the canes; in the Equisetum hyemale, or
Dutch rush; in the husk of rice, wheat, and other grains, silica in some form
or other is abundant. Some have beautifully-arranged masses of silica with
raphides. The leaves of Deutzia scabia, No. 7, are remarkable for their
stellate hairs, developed from the cuticle of both their upper and under
surfaces; forming most interesting and attractive objects examined under
polarised light. (Plate VIII., No. 173.)
Silica is found in the structure of Rubiaceæ both in the stem and leaves,
and, if present in sufficient thickness, depolarises light. This is especially
the case in the glandular hairs on the margins of the leaves. One of the order
Compositæ, a plant popularly known as the “sneezewort” (Archillæ
ptarmica), has a large amount of silica in the hairs found about the
serratures of its leaves.
All plants are provided with hairs; some few with hairs of a defensive
character. Those in the Urtica dioica, commonly called the Stinging-nettle,
are glandular hairs, developed from the cuticle, and contain an irritating
fluid; in other hairs a circulation is visible: examined under a power of 100
diameters, they present the appearance seen at Plate XIII., No. 19.
a stellate form, as in that of the grass (Pharus cristatus). (Plate XIV., No. 6.)
Raphides of peculiar figure are found in the bark of certain trees. In the
hickory (Carya alba) may be observed masses of flattened prisms having
both extremities pointed. In vertical sections from the stem of Elæagnus
angustifolia, numerous raphides of large size are embedded in the pith, and
also found in the bark of the apple-tree, and in elm seeds, every cell
containing two or more minute crystals.
In the Graminaceæ, especially the canes; in the Equisetum hyemale, or
Dutch rush; in the husk of rice, wheat, and other grains, silica in some form
or other is abundant. Some have beautifully-arranged masses of silica with
raphides. The leaves of Deutzia scabia, No. 7, are remarkable for their
stellate hairs, developed from the cuticle of both their upper and under
surfaces; forming most interesting and attractive objects examined under
polarised light. (Plate VIII., No. 173.)
Silica is found in the structure of Rubiaceæ both in the stem and leaves,
and, if present in sufficient thickness, depolarises light. This is especially
the case in the glandular hairs on the margins of the leaves. One of the order
Compositæ, a plant popularly known as the “sneezewort” (Archillæ
ptarmica), has a large amount of silica in the hairs found about the
serratures of its leaves.
All plants are provided with hairs; some few with hairs of a defensive
character. Those in the Urtica dioica, commonly called the Stinging-nettle,
are glandular hairs, developed from the cuticle, and contain an irritating
fluid; in other hairs a circulation is visible: examined under a power of 100
diameters, they present the appearance seen at Plate XIII., No. 19.
Page 553
Fig. 323.
A. Cotton; B. Fibres of Flax; C. Filaments of Silk; D. Wool of Sheep.
The fibrous tissue of plants is of great value in many manufactures. It
supplies material for our linens, cordage, paper, and other industries. This
tissue is remarkable for toughness of fibre, and exhibits an approach to
indestructibility, in the use it is put to in connection with the electric light. It
is of importance, then, to be able to distinguish it from other fibres with
which it is often mixed in various manufactures. Here the use of the
microscope is found of considerable importance. In flax and hemp, in which
the fibres are of great length, there are traces of transverse markings at short
intervals. In the rough condition in which flax is imported into this country,
the fibres have been separated, to a certain extent, by a process termed
hackling, and further subjected to hackling, maceration, and bleaching,
before it can be reduced to the white silky condition required by the spinner
and weaver, and finally assumes the appearance of structureless tubes, Fig.
323 B. China-grass, New Zealand flax, and some other plants produce a
similar material, but are not so strong, in consequence of the outer
membrane containing more lignine. It is important to the manufacturer that
he should be able to determine the true character of some of the textures
employed in articles of clothing; this he may do by the aid of the
microscope. In linen we find each component thread made up of the
longitudinal, unmarked fibres of flax; but if cotton has been mixed, we
recognise a flattened, more or less rounded band, as in Fig. 323 A, having a
very striking resemblance to hair, which, in reality, it is; since, in the
condition of elongated cells, it lines the inner surface of the pod. These,
again, should he contrasted with the filaments of silk, Fig. 323 C, and also
of wool, Fig. 323 D. The latter may be at once recognised by the zigzag
transverse markings on its fibres. The surface of wool is covered with
furrowed and twisted fine cross lines, of which there are from 2,000 to
4,000 in an inch. On this structure depends its felting property, in judging of
fleeces, attention should be paid to the fineness and elasticity of the fibre—
the furrowed and scaly surface, as shown by the microscope, the quantity of
fibre in a given surface, the purity of the fleece, upon which depend the
success of the scouring and subsequent operations.
A. Cotton; B. Fibres of Flax; C. Filaments of Silk; D. Wool of Sheep.
The fibrous tissue of plants is of great value in many manufactures. It
supplies material for our linens, cordage, paper, and other industries. This
tissue is remarkable for toughness of fibre, and exhibits an approach to
indestructibility, in the use it is put to in connection with the electric light. It
is of importance, then, to be able to distinguish it from other fibres with
which it is often mixed in various manufactures. Here the use of the
microscope is found of considerable importance. In flax and hemp, in which
the fibres are of great length, there are traces of transverse markings at short
intervals. In the rough condition in which flax is imported into this country,
the fibres have been separated, to a certain extent, by a process termed
hackling, and further subjected to hackling, maceration, and bleaching,
before it can be reduced to the white silky condition required by the spinner
and weaver, and finally assumes the appearance of structureless tubes, Fig.
323 B. China-grass, New Zealand flax, and some other plants produce a
similar material, but are not so strong, in consequence of the outer
membrane containing more lignine. It is important to the manufacturer that
he should be able to determine the true character of some of the textures
employed in articles of clothing; this he may do by the aid of the
microscope. In linen we find each component thread made up of the
longitudinal, unmarked fibres of flax; but if cotton has been mixed, we
recognise a flattened, more or less rounded band, as in Fig. 323 A, having a
very striking resemblance to hair, which, in reality, it is; since, in the
condition of elongated cells, it lines the inner surface of the pod. These,
again, should he contrasted with the filaments of silk, Fig. 323 C, and also
of wool, Fig. 323 D. The latter may be at once recognised by the zigzag
transverse markings on its fibres. The surface of wool is covered with
furrowed and twisted fine cross lines, of which there are from 2,000 to
4,000 in an inch. On this structure depends its felting property, in judging of
fleeces, attention should be paid to the fineness and elasticity of the fibre—
the furrowed and scaly surface, as shown by the microscope, the quantity of
fibre in a given surface, the purity of the fleece, upon which depend the
success of the scouring and subsequent operations.
Page 554
In the mummy-cloths of the
Egyptians flax only was used,
whereas the Peruvians used cotton
alone. By the many improvements
introduced into manufacturing
processes, flax has been reduced to
the fineness and texture of silk, and
even made to resemble other
materials.
Fossil Plants.—It is well known that
the primordial forests furnish a
number of families of plants familiar
to the modern algæologist. The cord-
like plant, Chorda filium, known as
“dead men’s ropes,” from its proving
fatal at times to the too adventurous
swimmer who gets entangled in its
Fig. 324.
thick wreaths, had a Lower Silurian
representative, known to 1. Woody Fibre from the root of the Elder,
palæontologists as Palæochorda, or exhibiting small pores; 2. Woody fibre of fossil
wood, showing large pores; 3. Woody fibre of
ancient chorda, which existed, fossil wood, bordered with pores and spiral
apparently, in two species,—a larger fibres; 4. Fossil wood from coal.
and a smaller. The still better known
Chondrus crispus, the Irish moss, or Carrageen moss, has likewise its
apparent, though more distant representative, in chondritis, a Lower
Silurian algal, of which there seems to exist at least three species. The
fucoids, or kelpweeds, appear to have also their representatives in such
plants as Fucoides gracilis, of the Lower Silurians of the Malverns; in
short, the Thallogens of the first ages of vegetable life seem to have
resembled in the group, and in at least their more prominent features, the
algæ of the existing time. And with the first indications of land we pass
from the thallogens to the acrogens—from the seaweeds to the fern-allies.
The Lycopodiaceæ, or club-mosses, bear in the axils of their leaves minute
circular cases, which form the receptacles of their spore-like seeds. And
when high in the Upper Silurian system, and just when preparing to quit it
for the Lower Old Red Sandstone, we detect our earliest terrestrial
Egyptians flax only was used,
whereas the Peruvians used cotton
alone. By the many improvements
introduced into manufacturing
processes, flax has been reduced to
the fineness and texture of silk, and
even made to resemble other
materials.
Fossil Plants.—It is well known that
the primordial forests furnish a
number of families of plants familiar
to the modern algæologist. The cord-
like plant, Chorda filium, known as
“dead men’s ropes,” from its proving
fatal at times to the too adventurous
swimmer who gets entangled in its
Fig. 324.
thick wreaths, had a Lower Silurian
representative, known to 1. Woody Fibre from the root of the Elder,
palæontologists as Palæochorda, or exhibiting small pores; 2. Woody fibre of fossil
wood, showing large pores; 3. Woody fibre of
ancient chorda, which existed, fossil wood, bordered with pores and spiral
apparently, in two species,—a larger fibres; 4. Fossil wood from coal.
and a smaller. The still better known
Chondrus crispus, the Irish moss, or Carrageen moss, has likewise its
apparent, though more distant representative, in chondritis, a Lower
Silurian algal, of which there seems to exist at least three species. The
fucoids, or kelpweeds, appear to have also their representatives in such
plants as Fucoides gracilis, of the Lower Silurians of the Malverns; in
short, the Thallogens of the first ages of vegetable life seem to have
resembled in the group, and in at least their more prominent features, the
algæ of the existing time. And with the first indications of land we pass
from the thallogens to the acrogens—from the seaweeds to the fern-allies.
The Lycopodiaceæ, or club-mosses, bear in the axils of their leaves minute
circular cases, which form the receptacles of their spore-like seeds. And
when high in the Upper Silurian system, and just when preparing to quit it
for the Lower Old Red Sandstone, we detect our earliest terrestrial
Page 555
organisms, we find that they are composed exclusively of those little spore-
receptacles.
The existing plants whence we derive our analogies in dealing with the
vegetation of this early period contribute but little, if at all, to the support of
animal life. The ferns and their allies remain untouched by the grazing
animals. Our native club-mosses, though once used in medicine, are
positively deleterious; horsetails (Equisetaceæ), though harmless, so
abound in silex, which wrap them round with a cuticle of stone, that they
are rarely cropped by cattle; while the thickets of fern which cover our hill
and dell, and seem so temptingly rich and green in their season, scarce
support the existence of a single creature, and remain untouched, in stem
and leaf, from their first appearance in spring until they droop and wither
under the frosts of early winter.
The flora of the coal measures was the richest and most luxuriant, in at least
individual productions, with which the fossil botanist has formed an
acquaintance. Never before or since did our planet bear so rank a vegetation
as that of which the numerous coal seams and inflammable shales of the
carboniferous period form but a portion of the remains—the portion spared,
in the first instance, by dissipation and decay, and in the second by
denuding agencies. Nevertheless almost all our coal—the stored-up fuel of
a world—is not, as it is often said to be, the product of destroyed forests of
conifers and flora of the profuse vegetation of the earliest periods in the
history of our globe. Later investigations show that our coal measures are
the compressed accumulations of peat-bogs which, layer by layer, have
sunken down under the superimposed weight of the next. The vertical stems
of coniferous trees became imbedded by a natural process of decay, and
were subsequently overwhelmed in the erect position in which they are
found. The true grasses scarcely appear in the fossil state at all. For the first
time, amid the remains of a flora that seems to have had but few flowers—
the Oolitic ages—do we detect, in a few broken fragments of the wings of
butterflies, decided traces of the flower-sucking insects. Not, however, until
we enter into the great Tertiary division do these become numerous. The
first bee makes its appearance in the amber of the Eocene, locked up
hermetically in its gem-like tomb—an embalmed corpse in a crystal coffin
—along with fragments of flower-bearing herbs and trees. Her tomb
receptacles.
The existing plants whence we derive our analogies in dealing with the
vegetation of this early period contribute but little, if at all, to the support of
animal life. The ferns and their allies remain untouched by the grazing
animals. Our native club-mosses, though once used in medicine, are
positively deleterious; horsetails (Equisetaceæ), though harmless, so
abound in silex, which wrap them round with a cuticle of stone, that they
are rarely cropped by cattle; while the thickets of fern which cover our hill
and dell, and seem so temptingly rich and green in their season, scarce
support the existence of a single creature, and remain untouched, in stem
and leaf, from their first appearance in spring until they droop and wither
under the frosts of early winter.
The flora of the coal measures was the richest and most luxuriant, in at least
individual productions, with which the fossil botanist has formed an
acquaintance. Never before or since did our planet bear so rank a vegetation
as that of which the numerous coal seams and inflammable shales of the
carboniferous period form but a portion of the remains—the portion spared,
in the first instance, by dissipation and decay, and in the second by
denuding agencies. Nevertheless almost all our coal—the stored-up fuel of
a world—is not, as it is often said to be, the product of destroyed forests of
conifers and flora of the profuse vegetation of the earliest periods in the
history of our globe. Later investigations show that our coal measures are
the compressed accumulations of peat-bogs which, layer by layer, have
sunken down under the superimposed weight of the next. The vertical stems
of coniferous trees became imbedded by a natural process of decay, and
were subsequently overwhelmed in the erect position in which they are
found. The true grasses scarcely appear in the fossil state at all. For the first
time, amid the remains of a flora that seems to have had but few flowers—
the Oolitic ages—do we detect, in a few broken fragments of the wings of
butterflies, decided traces of the flower-sucking insects. Not, however, until
we enter into the great Tertiary division do these become numerous. The
first bee makes its appearance in the amber of the Eocene, locked up
hermetically in its gem-like tomb—an embalmed corpse in a crystal coffin
—along with fragments of flower-bearing herbs and trees. Her tomb
Page 556
remains to testify to the gradual fitting up of our earth as a place of
habitation for creatures destined to seek delight for the mind and eye, as
certainly as for the proper senses, and in especial marks the introduction of
the stately forest trees, and the arrival of the charmingly beautiful flowers
that now deck the earth.62
habitation for creatures destined to seek delight for the mind and eye, as
certainly as for the proper senses, and in especial marks the introduction of
the stately forest trees, and the arrival of the charmingly beautiful flowers
that now deck the earth.62
Page 557
CHAPTER II.
The Sub-kingdom Protozoa.
The consideration of the whole special group of organisms forming the
subject matter of this chapter, under the heading of Protozoa, were formerly
included among Infusoria, which also embraced every kind of
microscopical aquatic body, whether belonging to the vegetable or animal
series. A more critical survey of the organisation and affinities of Infusoria
and the members which constituted the group led to a re-arrangement,
which has been very generally accepted as forming a sub-kingdom,
Protozoa. This may be defined as embracing all those forms of life,
referable to the lowest grade of the animal kingdom, whose members for
the most part are represented by organisms possessing a single cell or
aggregation of cells (and also included under the general term of unicellular
organisms) the whole of which are engaged in feeding, moving, respiring,
and reproducing by segmentation or fission much in the same way as that of
the unicellular plants described in a previous chapter. Following out this
sub-division of the entire series of Protozoa, the several groups range
themselves into four readily distinguishable sections. In the first, the most
lowly organised and most abundant have no oral orifice in the literal
meaning of the word, food being intercepted at any point of the surface of
the body. This most simple elementary type of structure of the Protozoa is
represented in the Amœba and Actinophrys, the various representatives of
the Foraminifera, and certain Flagellata, as Spumella and Anthrophysa.
Next in the ascending scale is a group of Protozoa, in which, though
differentiation has not proceeded so far as to arrive at the constitution of a
distinct oral aperture, the inception of food substance is limited to a
discoidal area occupying the anterior extremity of the body and is
associated with the special food-arresting apparatus. To this section of the
Protozoa are relegated the minuter flagellate, “collar-bearing” animals, and
also the entire group of sponges or Porifera.
The Sub-kingdom Protozoa.
The consideration of the whole special group of organisms forming the
subject matter of this chapter, under the heading of Protozoa, were formerly
included among Infusoria, which also embraced every kind of
microscopical aquatic body, whether belonging to the vegetable or animal
series. A more critical survey of the organisation and affinities of Infusoria
and the members which constituted the group led to a re-arrangement,
which has been very generally accepted as forming a sub-kingdom,
Protozoa. This may be defined as embracing all those forms of life,
referable to the lowest grade of the animal kingdom, whose members for
the most part are represented by organisms possessing a single cell or
aggregation of cells (and also included under the general term of unicellular
organisms) the whole of which are engaged in feeding, moving, respiring,
and reproducing by segmentation or fission much in the same way as that of
the unicellular plants described in a previous chapter. Following out this
sub-division of the entire series of Protozoa, the several groups range
themselves into four readily distinguishable sections. In the first, the most
lowly organised and most abundant have no oral orifice in the literal
meaning of the word, food being intercepted at any point of the surface of
the body. This most simple elementary type of structure of the Protozoa is
represented in the Amœba and Actinophrys, the various representatives of
the Foraminifera, and certain Flagellata, as Spumella and Anthrophysa.
Next in the ascending scale is a group of Protozoa, in which, though
differentiation has not proceeded so far as to arrive at the constitution of a
distinct oral aperture, the inception of food substance is limited to a
discoidal area occupying the anterior extremity of the body and is
associated with the special food-arresting apparatus. To this section of the
Protozoa are relegated the minuter flagellate, “collar-bearing” animals, and
also the entire group of sponges or Porifera.
Page 558
Gregarinida, Polycystina, Foraminifera, Rotifera, etc.
Tuffen West, del. Edmund Evans.
Plate III.
In the third section the highest degree of organisation is arrived at. Here is
represented a single, simple, often highly-differentiated oral aperture or true
mouth. Associated with this section are found the majority of those
organisms that collectively constitute the class Infusoria in the proper
acceptation of the term, and it embraces the majority of the Ciliata, the
Cilio-flagellata, as Euglena, Chilomonas, &c., in which the presence of a
distinct and circumscribed oral aperture is clearly seen. With the fourth and
remaining section of Protozoa, the oral or inceptive apparatus exhibits a
highly characteristic structural modification. This is not restricted to a
definite area, nor is it associated with the entire surface of the body, but it
Tuffen West, del. Edmund Evans.
Plate III.
In the third section the highest degree of organisation is arrived at. Here is
represented a single, simple, often highly-differentiated oral aperture or true
mouth. Associated with this section are found the majority of those
organisms that collectively constitute the class Infusoria in the proper
acceptation of the term, and it embraces the majority of the Ciliata, the
Cilio-flagellata, as Euglena, Chilomonas, &c., in which the presence of a
distinct and circumscribed oral aperture is clearly seen. With the fourth and
remaining section of Protozoa, the oral or inceptive apparatus exhibits a
highly characteristic structural modification. This is not restricted to a
definite area, nor is it associated with the entire surface of the body, but it
Page 559
consists of a number of flexible, retractile, tentacle-like organs radiating
from diverse and definite regions of the periphery, each of which subserves
as a tubular sucking-mouth, or for the purpose of grasping food. These may
be literally described as many-mouthed, and have been appropriately
designated Polystomata. The true zoological position of the Spongida or
Porifera is not finally settled, the members of this important section having
been formerly regarded as a subordinate group of the Rhizopoda or an
independent class of the Protozoa; consequently a tendency has been shown
to assign to them a position more nearly approximating to that of the
Cœlenterata, or zoophytes and corals, or place them among the more highly
organised tissue-constructed animals, the Metazoa, these being
characterised by groups of cells set apart to perform certain functions for
the whole animal. A division of labour is seen to be marked in these lower
animals as the organism becomes more specialised, and the number of
functions a cell performs becomes more and more limited as the body
becomes more complex.
It has been found convenient to adopt the following definition of the
Infusoria as one more generally acceptable. The Protozoa in their adult
condition are furnished with prehensile or locomotive organs, that take the
form of cilia, flagella, or of adhesive or suctorial tentacula, but not of
simple pseudopodia; their zooids are essentially unicellular, free swimming
or sedentary; they are either naked, loricate, or inhabit a simple,
mucilaginous matrix; single or united in aggregations, in which the
individual units are distinctly recognisable; not united and forming a single
gelatinous plasmodium, as in Mycetozoa, nor immersed within and lining
the interior cavities of a complex protoplasmic and mostly spiculiferous
skeleton, as in the Spongida, their food substances being intercepted by a
single distinct oral aperture, or by several apertures through a limited
terminal region or through the entire area of the general surface of the body.
They increase by simple longitudinal or transverse fission, by external or
internal gemmation or division, preceded mostly by a quiescent or encysted
state, into a greater or less number of sporular bodies. Sexual elements, as
represented by true ova or spermatozoa, are entirely absent, but two or more
zooids frequently coalesce as an antecedent process to the phenomena of
open formation.63
from diverse and definite regions of the periphery, each of which subserves
as a tubular sucking-mouth, or for the purpose of grasping food. These may
be literally described as many-mouthed, and have been appropriately
designated Polystomata. The true zoological position of the Spongida or
Porifera is not finally settled, the members of this important section having
been formerly regarded as a subordinate group of the Rhizopoda or an
independent class of the Protozoa; consequently a tendency has been shown
to assign to them a position more nearly approximating to that of the
Cœlenterata, or zoophytes and corals, or place them among the more highly
organised tissue-constructed animals, the Metazoa, these being
characterised by groups of cells set apart to perform certain functions for
the whole animal. A division of labour is seen to be marked in these lower
animals as the organism becomes more specialised, and the number of
functions a cell performs becomes more and more limited as the body
becomes more complex.
It has been found convenient to adopt the following definition of the
Infusoria as one more generally acceptable. The Protozoa in their adult
condition are furnished with prehensile or locomotive organs, that take the
form of cilia, flagella, or of adhesive or suctorial tentacula, but not of
simple pseudopodia; their zooids are essentially unicellular, free swimming
or sedentary; they are either naked, loricate, or inhabit a simple,
mucilaginous matrix; single or united in aggregations, in which the
individual units are distinctly recognisable; not united and forming a single
gelatinous plasmodium, as in Mycetozoa, nor immersed within and lining
the interior cavities of a complex protoplasmic and mostly spiculiferous
skeleton, as in the Spongida, their food substances being intercepted by a
single distinct oral aperture, or by several apertures through a limited
terminal region or through the entire area of the general surface of the body.
They increase by simple longitudinal or transverse fission, by external or
internal gemmation or division, preceded mostly by a quiescent or encysted
state, into a greater or less number of sporular bodies. Sexual elements, as
represented by true ova or spermatozoa, are entirely absent, but two or more
zooids frequently coalesce as an antecedent process to the phenomena of
open formation.63
Page 560
The infusorial body in its simplest type of development, as in Amœba,
exhibits a structural composition substantially corresponding with that of
the lowest organised tissue cell. There is no distinct bounding membrane, or
cell-wall, and it is throughout, and apart from the nucleus or endopart, one
continuous mass of granular matter, but otherwise homogeneous and
undifferentiated protoplasm. Professor Greef, who has made a study of the
Amœba, describes motor fibrils in the exoplasm which are active and large
in A. terricola. These are readily seen by staining with osmic acid, and,
after washing this out with water, immersing in a weak alcoholic solution.
In Amœba so prepared and examined with a high power, the whole body
will be seen to be surrounded by a distinct double integumentary layer.
Highly refractive bodies may also be seen in the interior, connected together
by extremely fine filaments. Professor Greef concludes that here we have to
do with muscular fibrillæ, which traverse the contractile outer zone in a
radial direction and there terminate for the time being. By a similar method,
axial filaments can be demonstrated in Heliozoa; these, it is believed, are
the true motors of their pseudopodia, and also the axial structures of the
Acineta, a marine animal related to ciliate infusoria.
In the Amœba, at one time well known as the Proteus animalcule, Fig. 325,
the marvellous body creeps onward in a flowing manner, occasionally and
languidly emitting a single pseudopod first on one side, then on the other.
More commonly it puts on a dendroid or palmate form; then again it
assumes more or less grotesque shapes in which almost any conceivable
image may be imagined. The body, as will be seen in this highly-magnified
figure, is full of granules (with the exception of a thin clear outer hyaline
zone), and near the centre is a globular or discoid body known as the
nucleus, composed of slightly denser material than that which surrounds it.
The division of the body into two is preceded by a division of this nucleus.
Near the latter is a clear spherical space—the contractile vacuole—which
gradually expands, and then rather suddenly collapses and reappears at the
same spot, the systole and diastole being slow and continuous. The
contractile vacuole contains a clear liquid which is expelled on the collapse
of the vacuole. This organ probably serves the double function of
respiration and excretion. The Amœba is omnivorous, chiefly a vegetarian,
and, therefore, found on the ooze of ponds or on the under surface of the
exhibits a structural composition substantially corresponding with that of
the lowest organised tissue cell. There is no distinct bounding membrane, or
cell-wall, and it is throughout, and apart from the nucleus or endopart, one
continuous mass of granular matter, but otherwise homogeneous and
undifferentiated protoplasm. Professor Greef, who has made a study of the
Amœba, describes motor fibrils in the exoplasm which are active and large
in A. terricola. These are readily seen by staining with osmic acid, and,
after washing this out with water, immersing in a weak alcoholic solution.
In Amœba so prepared and examined with a high power, the whole body
will be seen to be surrounded by a distinct double integumentary layer.
Highly refractive bodies may also be seen in the interior, connected together
by extremely fine filaments. Professor Greef concludes that here we have to
do with muscular fibrillæ, which traverse the contractile outer zone in a
radial direction and there terminate for the time being. By a similar method,
axial filaments can be demonstrated in Heliozoa; these, it is believed, are
the true motors of their pseudopodia, and also the axial structures of the
Acineta, a marine animal related to ciliate infusoria.
In the Amœba, at one time well known as the Proteus animalcule, Fig. 325,
the marvellous body creeps onward in a flowing manner, occasionally and
languidly emitting a single pseudopod first on one side, then on the other.
More commonly it puts on a dendroid or palmate form; then again it
assumes more or less grotesque shapes in which almost any conceivable
image may be imagined. The body, as will be seen in this highly-magnified
figure, is full of granules (with the exception of a thin clear outer hyaline
zone), and near the centre is a globular or discoid body known as the
nucleus, composed of slightly denser material than that which surrounds it.
The division of the body into two is preceded by a division of this nucleus.
Near the latter is a clear spherical space—the contractile vacuole—which
gradually expands, and then rather suddenly collapses and reappears at the
same spot, the systole and diastole being slow and continuous. The
contractile vacuole contains a clear liquid which is expelled on the collapse
of the vacuole. This organ probably serves the double function of
respiration and excretion. The Amœba is omnivorous, chiefly a vegetarian,
and, therefore, found on the ooze of ponds or on the under surface of the
Page 561
leaves of aquatic plants, especially among Confervæ. It can be readily
produced by placing a few fibres of fresh meat in an infusion of hay.
Fig. 325.—Amœba, Proteus animalcule; magnified 600 diameters.—(Warne).
The Gregarinæ consist of a remarkable group of organisms, but these,
although unicellular, are, for the most part, confined to the intestinal tract of
worms and of the higher animals, and will therefore be described among
internal parasites.
Tho fungus-animals, Mycetozoa, have already been referred to in a
previous chapter. The best known species, however, is found in tan yards in
the form of creeping masses of naked protoplasm, termed Plasmodia. Cakes
of protoplasm become segregated from the main mass, and break up into
Amœba-like spores, which unite again to form Plasmodia.
The Rhizopoda, or root-footed class of animals, are among the most
interesting simple organisms with which the microscope has made us
acquainted. In the living state they have the power of protruding
pseudopodia from the body, by which they creep about, or cling to plants
produced by placing a few fibres of fresh meat in an infusion of hay.
Fig. 325.—Amœba, Proteus animalcule; magnified 600 diameters.—(Warne).
The Gregarinæ consist of a remarkable group of organisms, but these,
although unicellular, are, for the most part, confined to the intestinal tract of
worms and of the higher animals, and will therefore be described among
internal parasites.
Tho fungus-animals, Mycetozoa, have already been referred to in a
previous chapter. The best known species, however, is found in tan yards in
the form of creeping masses of naked protoplasm, termed Plasmodia. Cakes
of protoplasm become segregated from the main mass, and break up into
Amœba-like spores, which unite again to form Plasmodia.
The Rhizopoda, or root-footed class of animals, are among the most
interesting simple organisms with which the microscope has made us
acquainted. In the living state they have the power of protruding
pseudopodia from the body, by which they creep about, or cling to plants
Page 562
when in search of food. This group,
in fact, includes Amœba,
Foraminifera, Sun-animalcules, and
Radiolarians. In the first the
pseudopodia are simple and lobose;
in the second they are slender,
confluent and reticulate; while in the
two last they are simple, radiating
and somewhat stiff, and partake of a
calcareous formation.
Of the Lobosa, we may take a well-
known representative of the group,
Fig. 326.—Rhizopoda lobosa. the Protomyxa, found at the bottom
of fresh-water pools, especially those
A. Difflugia proteiformis; B. Difflugia oblonga;
C, D. Arcella acuminata and dentata near bog-moss, where its minute
orange-coloured particles of jelly-
like substance are seen creeping over stones or shells. If quietly watched the
pseudopodia, some of which are broad and others slender, become
quiescent spheres, which break up into numerous portions, each of which
becomes a new animal.
This group is divided into the shell-less (Nuda) and shell-formed (Testacea).
The brown, horny covering is often finely faceted, and is either shaped like
a dome, semi-circular, or flat as a box, through which they protrude their
few or many pseudopodia (seen in Fig. 326).
PLATE XV.
in fact, includes Amœba,
Foraminifera, Sun-animalcules, and
Radiolarians. In the first the
pseudopodia are simple and lobose;
in the second they are slender,
confluent and reticulate; while in the
two last they are simple, radiating
and somewhat stiff, and partake of a
calcareous formation.
Of the Lobosa, we may take a well-
known representative of the group,
Fig. 326.—Rhizopoda lobosa. the Protomyxa, found at the bottom
of fresh-water pools, especially those
A. Difflugia proteiformis; B. Difflugia oblonga;
C, D. Arcella acuminata and dentata near bog-moss, where its minute
orange-coloured particles of jelly-
like substance are seen creeping over stones or shells. If quietly watched the
pseudopodia, some of which are broad and others slender, become
quiescent spheres, which break up into numerous portions, each of which
becomes a new animal.
This group is divided into the shell-less (Nuda) and shell-formed (Testacea).
The brown, horny covering is often finely faceted, and is either shaped like
a dome, semi-circular, or flat as a box, through which they protrude their
few or many pseudopodia (seen in Fig. 326).
PLATE XV.
Page 563
GROMIA.
In the Difflugia the lorica or shell is strengthened by the addition of
silicious particles; in Euglypta it is sac-shaped, with a jagged free margin,
the surface being covered by overlapping scales; while Arcella are capable
of secreting vesicles of air in their interior, whereby they are enabled to rise
to the surface. On some parts of our coast, if the sea sand be carefully
looked over with a pocket lens, there will often be found minute grains of a
porcelain oval kind, belonging to the Miliolina, segmented or strung
together not quite in the same plane.
In the Difflugia the lorica or shell is strengthened by the addition of
silicious particles; in Euglypta it is sac-shaped, with a jagged free margin,
the surface being covered by overlapping scales; while Arcella are capable
of secreting vesicles of air in their interior, whereby they are enabled to rise
to the surface. On some parts of our coast, if the sea sand be carefully
looked over with a pocket lens, there will often be found minute grains of a
porcelain oval kind, belonging to the Miliolina, segmented or strung
together not quite in the same plane.
Page 564
Fig. 327.—Section of Rotalia.
a,a, Radiating interceptal canals; b, Internal Fig. 328.—Rosalina varians or Discorbina
bifurcations; c, Transverse branch; d, Tubular globularia, with pseudopodia
wall of chambers. protruding.
The Foraminifera are rhizopods, whose simple protoplasmic bodies send
forth, through perforations in the membrane or outer covering of calcium
carbonate and silica, branching rays of pseudopodia. The order is divided
into two groups, the Imperforata and the Perforata; in the former the shell or
harder structure possesses only one or more apertures, whereas in the latter,
in addition to the main opening, the shell has its walls perforated
throughout, which admits of minute pseudopodia or fine threads being
protruded (Fig. 328). (See also Plate III., Nos. 75-85.) The vast majority of
Perforata form their shells, or rather skeletons, of calcium carbonate and
silica, which renders them almost indestructible. Consequently the form is
preserved through ages, and they present objects of the greatest interest to
the microscopist.
A curious and interesting feature of the Foraminifera—often an element of
difficulty to the student—is the tendency of modifications of types
comprising the larger groups to run into parallel isomorphous series. Thus,
if the entire class be roughly divided, as it sometimes has been, into three
orders, comprising respectively the forms characterised by porcellaneous,
arenaceous, and hyaline “tests,” the same general conformation and
arrangement of chambers will be found in each of the three series. The most
remarkable example, even among the smaller groups, is the Rotaliidæ, of
which three or four genera may be arranged in parallel lines, and in more or
a,a, Radiating interceptal canals; b, Internal Fig. 328.—Rosalina varians or Discorbina
bifurcations; c, Transverse branch; d, Tubular globularia, with pseudopodia
wall of chambers. protruding.
The Foraminifera are rhizopods, whose simple protoplasmic bodies send
forth, through perforations in the membrane or outer covering of calcium
carbonate and silica, branching rays of pseudopodia. The order is divided
into two groups, the Imperforata and the Perforata; in the former the shell or
harder structure possesses only one or more apertures, whereas in the latter,
in addition to the main opening, the shell has its walls perforated
throughout, which admits of minute pseudopodia or fine threads being
protruded (Fig. 328). (See also Plate III., Nos. 75-85.) The vast majority of
Perforata form their shells, or rather skeletons, of calcium carbonate and
silica, which renders them almost indestructible. Consequently the form is
preserved through ages, and they present objects of the greatest interest to
the microscopist.
A curious and interesting feature of the Foraminifera—often an element of
difficulty to the student—is the tendency of modifications of types
comprising the larger groups to run into parallel isomorphous series. Thus,
if the entire class be roughly divided, as it sometimes has been, into three
orders, comprising respectively the forms characterised by porcellaneous,
arenaceous, and hyaline “tests,” the same general conformation and
arrangement of chambers will be found in each of the three series. The most
remarkable example, even among the smaller groups, is the Rotaliidæ, of
which three or four genera may be arranged in parallel lines, and in more or
Page 565
less closely isomorphous series. In the report appended to the “Challenger”
scheme of classification many examples are enumerated. In Arenacea we
have a small family of Foraminifera, the external surfaces of which present
a ridge and furrow arrangement, and the incrustations are entirely of a
sandy nature held together by a cement secreted by the animal. (Plate XV.,
No. 1, Astrorhiza limicola.)
Gromia.—Among the more remarkable of the Perforata group the Gromia
have a foremost place. They are very minute globular or oval-shaped
bodies, about one-twenty-fourth of an inch in length, found in fresh,
brackish, and salt water. The forms brought up in Dr. Wallich’s deep sea
soundings of 1860 were taken attached to pieces of corallines, or found
loose among Globigerina ooze. At first there appears to be nothing peculiar
about these tiny specks of matter resembling the ova of a zoophyte, but
presently, at the smaller end, a very fine thread is protruded, and then
another, dividing into finer branches, and, ultimately, a complete network of
filaments extends on all sides, and become attached to the side of the glass
jar that contains them. Now, on employing magnifying power, every thread
exhibits a circulatory motion, an up and down stream or cyclosis of
granules suspended in a fluid mass. It is by means of these pseudopodia, as
the threads are termed, that the Gromia moves its body along and clings to
the glass. We may surmise, then, that these pseudopodia are either
gelatinous, glutinous, or terminate in sucker-like processes. Increase in the
“test,” integument, is brought about, as in Difflugia, by the secretion of
calcareous matter or by cementing fine silicious particles to the outer wall,
as the protoplasm is seen to flow over the test, so that when it comes in
contact with a diatom it is thereby drawn towards the oral opening and
slowly digested.
Some considerable time elapsed between the discovery of Gromia by Mr.
W. Archer, F.R.S., and the demonstration of a nucleus and contractile
vesicle by Dr. Wallich. It was thought that in the whole of the Monozoa the
nucleus was absent, but it is now known that this important body is
embedded in the protoplasmic substance, and the reproduction of these
curious animals is thereby secured. Among the better known species of
Gromia is G. Dujardinii, chiefly distinguishable by the darker colour of the
“test,” by the greater quantity of silica that enters into the formation of its
scheme of classification many examples are enumerated. In Arenacea we
have a small family of Foraminifera, the external surfaces of which present
a ridge and furrow arrangement, and the incrustations are entirely of a
sandy nature held together by a cement secreted by the animal. (Plate XV.,
No. 1, Astrorhiza limicola.)
Gromia.—Among the more remarkable of the Perforata group the Gromia
have a foremost place. They are very minute globular or oval-shaped
bodies, about one-twenty-fourth of an inch in length, found in fresh,
brackish, and salt water. The forms brought up in Dr. Wallich’s deep sea
soundings of 1860 were taken attached to pieces of corallines, or found
loose among Globigerina ooze. At first there appears to be nothing peculiar
about these tiny specks of matter resembling the ova of a zoophyte, but
presently, at the smaller end, a very fine thread is protruded, and then
another, dividing into finer branches, and, ultimately, a complete network of
filaments extends on all sides, and become attached to the side of the glass
jar that contains them. Now, on employing magnifying power, every thread
exhibits a circulatory motion, an up and down stream or cyclosis of
granules suspended in a fluid mass. It is by means of these pseudopodia, as
the threads are termed, that the Gromia moves its body along and clings to
the glass. We may surmise, then, that these pseudopodia are either
gelatinous, glutinous, or terminate in sucker-like processes. Increase in the
“test,” integument, is brought about, as in Difflugia, by the secretion of
calcareous matter or by cementing fine silicious particles to the outer wall,
as the protoplasm is seen to flow over the test, so that when it comes in
contact with a diatom it is thereby drawn towards the oral opening and
slowly digested.
Some considerable time elapsed between the discovery of Gromia by Mr.
W. Archer, F.R.S., and the demonstration of a nucleus and contractile
vesicle by Dr. Wallich. It was thought that in the whole of the Monozoa the
nucleus was absent, but it is now known that this important body is
embedded in the protoplasmic substance, and the reproduction of these
curious animals is thereby secured. Among the better known species of
Gromia is G. Dujardinii, chiefly distinguishable by the darker colour of the
“test,” by the greater quantity of silica that enters into the formation of its
Page 566
pseudopodia, and by the formation of isogamous zoospores, two of which
are seen in conjugation in Plate XV., No. 2. An excess of protoplasm must
also be secreted to admit of so large a protrusion outside the testa.
G. Lieberkühnia (of Claparède and Lachman), No. 5, differs in formation.
Its shape is pyriform, and the opening whence the pseudopodia streams out
is situated in a lateral depression about midway in the testa, c, o. Hence a
trunk branch is seen to issue forth, and from this a ramification of threads,
psdp, extends to a considerable distance in all directions.
The Micro-gromia of Hertwig, No. 4, is the minutest form of the genus yet
discovered, and differs from those already described in the mode of
reproduction. The individual takes the shape of a water bottle with a short
neck, whence issue forth a limited number of very slender threads. The test
is quite transparent, and it was in this species that the nucleus and
contractile vesicle, which lie embedded near the mouth, were first clearly
made out.
The zoospores of Micro-gromia have a curious habit of uniting with their
neighbours to form a colony, No. 4. Their colonisation is apparently
intended to facilitate multiplication. Reproduction is carried on somewhat
after the manner of Volvox. The globular bodies formed sink to the bottom
of the glass vessel, and there remain for a time in a quiescent state. In the
course of a day or two the mass assumes a motive appearance, increases in
bulk, becomes more ovoid in shape, and ultimately the nucleus shows the
first sign of division. Vertical segmentation takes place, as at A, into two
equal parts; each half is seen to possess its fair share of the nucleus and
contractile vesicle. It then turns in the horizontal direction, and now there
appears to be an upper and a lower division, the uppermost having a neck-
like attachment, and this is making its way to the narrow oral opening in the
parent testa, as at B. Here it is seen pressing forward, and at C the neck is
protruding some distance, and the second half assumes a bottle shape; at D
the greater part of the animal is nearly set free, and after a short rest it fully
launches forth. It finally pulls itself together, as at E, and either develops a
pair of flagella and swims off, or assumes the form of an Actinophrys. In
either case, and in a very short space of time, the separated young animal is
are seen in conjugation in Plate XV., No. 2. An excess of protoplasm must
also be secreted to admit of so large a protrusion outside the testa.
G. Lieberkühnia (of Claparède and Lachman), No. 5, differs in formation.
Its shape is pyriform, and the opening whence the pseudopodia streams out
is situated in a lateral depression about midway in the testa, c, o. Hence a
trunk branch is seen to issue forth, and from this a ramification of threads,
psdp, extends to a considerable distance in all directions.
The Micro-gromia of Hertwig, No. 4, is the minutest form of the genus yet
discovered, and differs from those already described in the mode of
reproduction. The individual takes the shape of a water bottle with a short
neck, whence issue forth a limited number of very slender threads. The test
is quite transparent, and it was in this species that the nucleus and
contractile vesicle, which lie embedded near the mouth, were first clearly
made out.
The zoospores of Micro-gromia have a curious habit of uniting with their
neighbours to form a colony, No. 4. Their colonisation is apparently
intended to facilitate multiplication. Reproduction is carried on somewhat
after the manner of Volvox. The globular bodies formed sink to the bottom
of the glass vessel, and there remain for a time in a quiescent state. In the
course of a day or two the mass assumes a motive appearance, increases in
bulk, becomes more ovoid in shape, and ultimately the nucleus shows the
first sign of division. Vertical segmentation takes place, as at A, into two
equal parts; each half is seen to possess its fair share of the nucleus and
contractile vesicle. It then turns in the horizontal direction, and now there
appears to be an upper and a lower division, the uppermost having a neck-
like attachment, and this is making its way to the narrow oral opening in the
parent testa, as at B. Here it is seen pressing forward, and at C the neck is
protruding some distance, and the second half assumes a bottle shape; at D
the greater part of the animal is nearly set free, and after a short rest it fully
launches forth. It finally pulls itself together, as at E, and either develops a
pair of flagella and swims off, or assumes the form of an Actinophrys. In
either case, and in a very short space of time, the separated young animal is
Page 567
quite ready to re-unite, as at F, and assist in forming a new colony of the
species.
The Polymorphina belong to a low genus of the Foraminifera. They consist
of a number of forms and exhibit a rather extensive series of variations,
although consisting of a few simple types, and showing transitions between
forms which at first seem to be distinct. The majority of species keep to the
sea bottom; some few are pelagic, and occur in abundance on the surface of
the ocean. Among the latter are the Globigerina: its shell is about one-
fortieth of an inch in diameter, and usually composed of seven globular
chambers arranged spirally in such a manner that all are visible from above,
each chamber opening by a crescentic-shaped orifice into a depression in
the middle of the next. Perfect specimens bristle with long slender spines,
the pores affording passage to pseudopodia, which stream out along the
spines. The more carefully-conducted deep-sea investigations have brought
to light the fact that the floor of the ocean, at great depths, and over a vast
area, is formed of these white or pinkish coloured bodies, all containing on
an average about 60 per cent. of calcium carbonate. It is a question whether
the Globigerinidæ which make up the bulk of the ooze actually live at the
bottom as well as the surface of the sea. This question has given rise to
much discussion. Dr. Murray came to the conclusion that pelagic species do
not live near the ocean floor. This opinion is partly based on the fact that the
area of the Globigerina ooze coincides with the area of surface of
temperature at which these bodies are found to exist. When the surface
water is too cold for them, they are not to be found, neither are they found
below. Major S. R. J. Owen, while dredging the surface of mid-ocean—the
Indian, and the warmer portion of the Atlantic—found attached to his nets a
number of these interesting bodies, and which always made their
appearance just about sunset. In Plate III., Nos. 43-52, a number of these
interesting and variously-formed bodies are given, and an attempt is also
made to show the richly-tinted colour appearances presented by the sarcode
or protoplasm of the Globigerina.
species.
The Polymorphina belong to a low genus of the Foraminifera. They consist
of a number of forms and exhibit a rather extensive series of variations,
although consisting of a few simple types, and showing transitions between
forms which at first seem to be distinct. The majority of species keep to the
sea bottom; some few are pelagic, and occur in abundance on the surface of
the ocean. Among the latter are the Globigerina: its shell is about one-
fortieth of an inch in diameter, and usually composed of seven globular
chambers arranged spirally in such a manner that all are visible from above,
each chamber opening by a crescentic-shaped orifice into a depression in
the middle of the next. Perfect specimens bristle with long slender spines,
the pores affording passage to pseudopodia, which stream out along the
spines. The more carefully-conducted deep-sea investigations have brought
to light the fact that the floor of the ocean, at great depths, and over a vast
area, is formed of these white or pinkish coloured bodies, all containing on
an average about 60 per cent. of calcium carbonate. It is a question whether
the Globigerinidæ which make up the bulk of the ooze actually live at the
bottom as well as the surface of the sea. This question has given rise to
much discussion. Dr. Murray came to the conclusion that pelagic species do
not live near the ocean floor. This opinion is partly based on the fact that the
area of the Globigerina ooze coincides with the area of surface of
temperature at which these bodies are found to exist. When the surface
water is too cold for them, they are not to be found, neither are they found
below. Major S. R. J. Owen, while dredging the surface of mid-ocean—the
Indian, and the warmer portion of the Atlantic—found attached to his nets a
number of these interesting bodies, and which always made their
appearance just about sunset. In Plate III., Nos. 43-52, a number of these
interesting and variously-formed bodies are given, and an attempt is also
made to show the richly-tinted colour appearances presented by the sarcode
or protoplasm of the Globigerina.
Page 568
Fig. 329.—Globigerina and other bodies taken in deep sea soundings (Atlantic).
“Many of the forms,” writes Major Owen,64 “have hitherto been claimed by
the geologist, but I have found them enjoying life in this their true home,
the silicious shells filled with coloured sarcode, and sometimes this sarcode
in a state of distension somewhat similar to that found projecting from the
Foraminifera, but not in such slender threads. There are no objects in nature
more brilliant in their colouring or more exquisitely delicate in their forms
and structure. Some are of but one colour, crimson, yellow, or blue;
sometimes two colours are found on the same individual, but always
separate, and rarely if ever mixed to form green or purple. In a globular
species, whose shell is made up of the most delicate fretwork, the brilliant
colours of the sarcode shine through the little perforations very prettily. In
specimens of the triangular and square forms (Plate III., Nos. 43, 44, 45 and
“Many of the forms,” writes Major Owen,64 “have hitherto been claimed by
the geologist, but I have found them enjoying life in this their true home,
the silicious shells filled with coloured sarcode, and sometimes this sarcode
in a state of distension somewhat similar to that found projecting from the
Foraminifera, but not in such slender threads. There are no objects in nature
more brilliant in their colouring or more exquisitely delicate in their forms
and structure. Some are of but one colour, crimson, yellow, or blue;
sometimes two colours are found on the same individual, but always
separate, and rarely if ever mixed to form green or purple. In a globular
species, whose shell is made up of the most delicate fretwork, the brilliant
colours of the sarcode shine through the little perforations very prettily. In
specimens of the triangular and square forms (Plate III., Nos. 43, 44, 45 and
Page 569
46), the respective tints of yellow and crimson are vivid and delicately
shaded; in one the pink lines are concentric; while another is of a stellate
form, the points and uncoloured parts being bright clear crystal, while a
beautiful crimson ring surrounds the central portion. A globular form
resembles a specimen of the Chinese ball-cutting—one sphere within
another; this, however, appears to belong to a distinct species.
Fig. 330.—Globigerina and other bodies taken in deep sea soundings, 1856
(Atlantic).
“The shells of some of the globular forms of these Polycystina, whose
conjugation I believe I have witnessed, are composed of a fine fretwork,
with one or more large circular holes; and I suspect the junction to take
place by the union of two such apertures. That the figures of these shells
become elongated, lose their globular form after death, and present a
shaded; in one the pink lines are concentric; while another is of a stellate
form, the points and uncoloured parts being bright clear crystal, while a
beautiful crimson ring surrounds the central portion. A globular form
resembles a specimen of the Chinese ball-cutting—one sphere within
another; this, however, appears to belong to a distinct species.
Fig. 330.—Globigerina and other bodies taken in deep sea soundings, 1856
(Atlantic).
“The shells of some of the globular forms of these Polycystina, whose
conjugation I believe I have witnessed, are composed of a fine fretwork,
with one or more large circular holes; and I suspect the junction to take
place by the union of two such apertures. That the figures of these shells
become elongated, lose their globular form after death, and present a
Page 570
disturbed surface is seen in some of the figures represented in Plate III.,
Nos. 82-85.” Those without internal chambers have been described as
Orbulina universa, Plate III., Fig. 78, while Nos. 75 and 76, although
members of the same family, have been separated, but all should certainly
be united under Globigerina.
“The minute silicious shells of Polycystina present wonderful beauty and
variety of form; all are more or less perforated, and often prolonged into
spines or other projections, through which the sarcode body extends itself
into pseudopodial prolongations resembling those of Actinophrys. When
seen disporting themselves in all their living splendour, their brilliancy of
colouring renders them objects of unusual attraction. It will appear that they
wish to avoid the light, as they are rarely found on the surface of the sea in
the daytime; it is after sunset and during the twilight that they make their
appearance.”
Many forms of Globigerina and Foraminifera are represented in Figs. 329
and 330. These varied and beautiful forms were dredged up with soundings
made in 1856 for the purpose of ascertaining the depth of the Atlantic, prior
to the laying down of the electric telegraph wire from England to America,
and taken at a depth of 2,070 fathoms.
Heliozoa.—Actinophrys-Sol, “sun-animalcules,” belong to this group; most
of them inhabit fresh water (Plate III., No. 66). The chief characteristic, and
the one to which they owe their name, is the possession of long, slender,
somewhat stiff pseudopodia; these radiate from all parts of the body. The
living animal usually contains green-coloured particles within a minute
translucent spherical globule of about 1⁄250th of an inch in diameter. It is,
therefore, variously designated the green sun-animalcule, Acanthocystis, or
Actinophrys-Sol. It is commonly found amongst the weeds in clear pools of
water, where desmids abound. The pseudopodia appear to be stiff; they are,
however, quite flexible, and the body contains more than one clear vesicle
with a nucleus; reproduction is secured by the simple division commencing
in the nucleus. The little animal can move over a hard surface by the
alternate relaxation and stiffening of its pseudopodia; when one of these
touches a small organism, it is believed to paralyse it, then envelop, and
deliberately digest it. In another species, the lattice-animalcule (Cathrulina),
Nos. 82-85.” Those without internal chambers have been described as
Orbulina universa, Plate III., Fig. 78, while Nos. 75 and 76, although
members of the same family, have been separated, but all should certainly
be united under Globigerina.
“The minute silicious shells of Polycystina present wonderful beauty and
variety of form; all are more or less perforated, and often prolonged into
spines or other projections, through which the sarcode body extends itself
into pseudopodial prolongations resembling those of Actinophrys. When
seen disporting themselves in all their living splendour, their brilliancy of
colouring renders them objects of unusual attraction. It will appear that they
wish to avoid the light, as they are rarely found on the surface of the sea in
the daytime; it is after sunset and during the twilight that they make their
appearance.”
Many forms of Globigerina and Foraminifera are represented in Figs. 329
and 330. These varied and beautiful forms were dredged up with soundings
made in 1856 for the purpose of ascertaining the depth of the Atlantic, prior
to the laying down of the electric telegraph wire from England to America,
and taken at a depth of 2,070 fathoms.
Heliozoa.—Actinophrys-Sol, “sun-animalcules,” belong to this group; most
of them inhabit fresh water (Plate III., No. 66). The chief characteristic, and
the one to which they owe their name, is the possession of long, slender,
somewhat stiff pseudopodia; these radiate from all parts of the body. The
living animal usually contains green-coloured particles within a minute
translucent spherical globule of about 1⁄250th of an inch in diameter. It is,
therefore, variously designated the green sun-animalcule, Acanthocystis, or
Actinophrys-Sol. It is commonly found amongst the weeds in clear pools of
water, where desmids abound. The pseudopodia appear to be stiff; they are,
however, quite flexible, and the body contains more than one clear vesicle
with a nucleus; reproduction is secured by the simple division commencing
in the nucleus. The little animal can move over a hard surface by the
alternate relaxation and stiffening of its pseudopodia; when one of these
touches a small organism, it is believed to paralyse it, then envelop, and
deliberately digest it. In another species, the lattice-animalcule (Cathrulina),
Page 571
the pseudopodia or silicious threads are arranged tangentially. It grows on a
long flexible stalk, attached to an aquatic plant, the total length of which is
about 1⁄200th an inch. The globular body is perforated in all directions,
through which the fine stiff pseudopodia are thrust out; it is often known to
form colonies.
In this order may well be placed the Radiolaria; they are, however, usually
separated. But Radiolarians, whether seen alive or in their skeleton form,
are surpassingly beautiful. By the favour of Messrs. Warne, I am enabled to
append a frontispiece plate to this volume taken from their “Royal Natural
History.” These bodies are all marine, and live in zones of several thousand
fathoms, and like their congeners, the Globigerina, they avoid a strong light,
and only appear after sunset. Their bodies are supposed to emit a
phosphorescent glow, but more is known of their silicious skeletons than of
their living forms; yet it is not this feature that separates them from other
orders of rhizopods, but the possession of a membranous central capsule
enclosing the nucleus. The body substance outside this capsule is highly
vacuolated in some species, especially in surface forms. A few are without a
skeleton, and these consist of oval masses of protoplasm, with slender
pseudopodia. In a few species the skeleton is formed of a glassy horny
substance, termed acanthin, arranged in the form of radiating spines.
Radiolarians secrete a silicious skeleton, which assumes a variety of forms,
as trellis-work, boxes joined by radiating spines, helmets, baskets, bee-
hives, discs, rings, and numerous other forms. Haeckel has described
upwards of four thousand species, and possibly as many more could be
added to this number. Radiolaria are divided into two groups. In the one
there is either no skeleton or one of silex; in the other the skeleton is formed
of radiating spines of a horny nature. These are again subdivided according
to the characters of the central capsule. In those forms with a silicious
skeleton the geometrical pattern conforms more or less to the shape of the
central capsule, being either spherical or conical. The central capsule is
regarded as being homologous with the calcareous shell of Globigerina.
Reproduction takes place by simple division into two, or by the body
breaking up into spores, each provided with a flagellum, or two spores may
fuse together, and the result will be an adult Radiolarian. Certain yellow
corpuscles present in the outer part of their body-surface change into
long flexible stalk, attached to an aquatic plant, the total length of which is
about 1⁄200th an inch. The globular body is perforated in all directions,
through which the fine stiff pseudopodia are thrust out; it is often known to
form colonies.
In this order may well be placed the Radiolaria; they are, however, usually
separated. But Radiolarians, whether seen alive or in their skeleton form,
are surpassingly beautiful. By the favour of Messrs. Warne, I am enabled to
append a frontispiece plate to this volume taken from their “Royal Natural
History.” These bodies are all marine, and live in zones of several thousand
fathoms, and like their congeners, the Globigerina, they avoid a strong light,
and only appear after sunset. Their bodies are supposed to emit a
phosphorescent glow, but more is known of their silicious skeletons than of
their living forms; yet it is not this feature that separates them from other
orders of rhizopods, but the possession of a membranous central capsule
enclosing the nucleus. The body substance outside this capsule is highly
vacuolated in some species, especially in surface forms. A few are without a
skeleton, and these consist of oval masses of protoplasm, with slender
pseudopodia. In a few species the skeleton is formed of a glassy horny
substance, termed acanthin, arranged in the form of radiating spines.
Radiolarians secrete a silicious skeleton, which assumes a variety of forms,
as trellis-work, boxes joined by radiating spines, helmets, baskets, bee-
hives, discs, rings, and numerous other forms. Haeckel has described
upwards of four thousand species, and possibly as many more could be
added to this number. Radiolaria are divided into two groups. In the one
there is either no skeleton or one of silex; in the other the skeleton is formed
of radiating spines of a horny nature. These are again subdivided according
to the characters of the central capsule. In those forms with a silicious
skeleton the geometrical pattern conforms more or less to the shape of the
central capsule, being either spherical or conical. The central capsule is
regarded as being homologous with the calcareous shell of Globigerina.
Reproduction takes place by simple division into two, or by the body
breaking up into spores, each provided with a flagellum, or two spores may
fuse together, and the result will be an adult Radiolarian. Certain yellow
corpuscles present in the outer part of their body-surface change into
Page 572
unicellular parasitic algals; these can be separated and cultivated
independently of their host. The Radiolarians live floating at all depths from
1,000 to 2,500 fathoms, and are distributed over areas in the central Pacific
and the south-eastern part of the Indian Ocean, the ooze forming the ocean
bed being made up of their skeletons to an extent of 80 per cent. of the
deposit; hence it has become known as Radiolarian ooze. The chalky-
looking Barbadoes earth, a Tertiary formation, is composed almost entirely
of their skeletons. Somewhat similar deposits exist in the Nicobar Islands,
in Greece, and in Sicily.
It will have been noticed that by far the greater number of Foraminifera are
of marine origin, and these occur in such widespread profusion that the
finest calcareous particles which constitute the seashore in some places
consist almost wholly of their microscopic remains. At former periods of
the earth’s history they appear to have existed even in greater profusion
than at the present time. This is evidenced by their remains forming the
principal constituent of our largest geological formations.
Moreover, during the Canadian Geological Survey large masses of what
appeared to be a fossil organism were discovered in rocks situated near the
base of the Laurentian series of North America. Sir William Dawson, of
Montreal, referred these remains to an animal of the foraminiferal type; and
specimens were sent by Sir W. Logan to the late Dr. Carpenter, requesting
him to subject them to a careful examination. As far back as 1858 Sir W.
Logan had suspected the existence of organic remains in specimens from
the Grand Calumet limestone, on the Ottawa River, but a casual
examination of the specimens was insufficient to determine the point.
Similar forms being seen by Sir W. Logan in blocks from the Grenville bed
of the Laurentian limestone were in their turn tried, and ultimately revealed
their true structure to Sir William Dawson and Dr. Sterry Hunt, who named
the structure Eozoon Canadense.
The masses of which these fossils consist are composed of layers of
serpentine alternating with calc spar. It was found by these observers that
the calcareous layers represented the original shell, and the silicious layers
the softer parts of the once living Foraminifera. The results were arrived at
through comparison of the appearance presented by the Eozoon with the
independently of their host. The Radiolarians live floating at all depths from
1,000 to 2,500 fathoms, and are distributed over areas in the central Pacific
and the south-eastern part of the Indian Ocean, the ooze forming the ocean
bed being made up of their skeletons to an extent of 80 per cent. of the
deposit; hence it has become known as Radiolarian ooze. The chalky-
looking Barbadoes earth, a Tertiary formation, is composed almost entirely
of their skeletons. Somewhat similar deposits exist in the Nicobar Islands,
in Greece, and in Sicily.
It will have been noticed that by far the greater number of Foraminifera are
of marine origin, and these occur in such widespread profusion that the
finest calcareous particles which constitute the seashore in some places
consist almost wholly of their microscopic remains. At former periods of
the earth’s history they appear to have existed even in greater profusion
than at the present time. This is evidenced by their remains forming the
principal constituent of our largest geological formations.
Moreover, during the Canadian Geological Survey large masses of what
appeared to be a fossil organism were discovered in rocks situated near the
base of the Laurentian series of North America. Sir William Dawson, of
Montreal, referred these remains to an animal of the foraminiferal type; and
specimens were sent by Sir W. Logan to the late Dr. Carpenter, requesting
him to subject them to a careful examination. As far back as 1858 Sir W.
Logan had suspected the existence of organic remains in specimens from
the Grand Calumet limestone, on the Ottawa River, but a casual
examination of the specimens was insufficient to determine the point.
Similar forms being seen by Sir W. Logan in blocks from the Grenville bed
of the Laurentian limestone were in their turn tried, and ultimately revealed
their true structure to Sir William Dawson and Dr. Sterry Hunt, who named
the structure Eozoon Canadense.
The masses of which these fossils consist are composed of layers of
serpentine alternating with calc spar. It was found by these observers that
the calcareous layers represented the original shell, and the silicious layers
the softer parts of the once living Foraminifera. The results were arrived at
through comparison of the appearance presented by the Eozoon with the
Page 573
microscopic structure which Dr. Carpenter had previously shown to
characterise certain members of the Foraminifera. The Eozoon not only
exceeded other known Foraminifera in size to an extent that might have
easily led observers astray, but, from its apparently very irregular mode of
growth and general external form, no help was derived in its identification,
and it was only by microscopical examination of its minute structure that its
true character was ascertained. Dr. Carpenter wrote:—“The minute
structure of Eozoon may be determined by the microscopic examination
either of thin transparent sections, or of portions which have been subjected
to the action of dilute acids, so as to remove the calcareous portion, leaving
only the internal casts, or models, in silex, of the chambers and other
cavities originally occupied by the substance of one animal.” Subsequently
he found portions of minute structure so perfect that he was able to say that
“delicate pseudopodial threads were originally put forth through openings
in the shell wall of less than 1⁄10000th of an inch in diameter” (Plate III., Nos.
64, 65). In a paper read at the meeting of the Geological Society he stated
that he had since detected Eozoon in a specimen of ophicalcite from
Bohemia, in a specimen of gneiss from near Moldau, and in specimens of
serpentine limestone sent to Sir C. Lyell by Dr. Gümbel, of Bavaria. These
also were found to be parts of the great formation of the “fundamental”
gneiss, considered by Sir Roderick Murchison as the equivalent of the
Laurentian rocks of Canada.65
If the remains of Foraminifera be dissolved in dilute hydrochloric acid, an
organic basis is left, after the removal of the calcareous matter, accurately
retaining the form of the shell with all its openings and pores. The earthy
constituent is mainly calcium carbonate; but there is also a small amount of
phosphate of lime in the shells of many of them.
characterise certain members of the Foraminifera. The Eozoon not only
exceeded other known Foraminifera in size to an extent that might have
easily led observers astray, but, from its apparently very irregular mode of
growth and general external form, no help was derived in its identification,
and it was only by microscopical examination of its minute structure that its
true character was ascertained. Dr. Carpenter wrote:—“The minute
structure of Eozoon may be determined by the microscopic examination
either of thin transparent sections, or of portions which have been subjected
to the action of dilute acids, so as to remove the calcareous portion, leaving
only the internal casts, or models, in silex, of the chambers and other
cavities originally occupied by the substance of one animal.” Subsequently
he found portions of minute structure so perfect that he was able to say that
“delicate pseudopodial threads were originally put forth through openings
in the shell wall of less than 1⁄10000th of an inch in diameter” (Plate III., Nos.
64, 65). In a paper read at the meeting of the Geological Society he stated
that he had since detected Eozoon in a specimen of ophicalcite from
Bohemia, in a specimen of gneiss from near Moldau, and in specimens of
serpentine limestone sent to Sir C. Lyell by Dr. Gümbel, of Bavaria. These
also were found to be parts of the great formation of the “fundamental”
gneiss, considered by Sir Roderick Murchison as the equivalent of the
Laurentian rocks of Canada.65
If the remains of Foraminifera be dissolved in dilute hydrochloric acid, an
organic basis is left, after the removal of the calcareous matter, accurately
retaining the form of the shell with all its openings and pores. The earthy
constituent is mainly calcium carbonate; but there is also a small amount of
phosphate of lime in the shells of many of them.
Page 574
Fig. 331.
1. Separated prisms from outer layer of Pinna shell; 2. Skeletons of Foraminifera
from limestone; 3. Recent shell of Polystomella crispa; examined under dark-
ground illumination.
Infusoria.
We are now brought face to face with animals which possess considerable
variation of structure, Infusorial animalcules, as they are termed. It was
Ehrenberg who attributed to them a highly complex organisation, but later
observations negatived these views and showed them to be animals formed
of one or more cells, or colonies of so-called individuals. It is true that this
cell or united protoplasm may show a wonderful amount of differentiation,
what with its nucleus and vacuole, mouth and gullet, its variously-arranged
cilia or flagella, its contractile fibres, its separation into an outer denser and
a more fluid inner protoplasm, and its horny cup and stalks.
1. Separated prisms from outer layer of Pinna shell; 2. Skeletons of Foraminifera
from limestone; 3. Recent shell of Polystomella crispa; examined under dark-
ground illumination.
Infusoria.
We are now brought face to face with animals which possess considerable
variation of structure, Infusorial animalcules, as they are termed. It was
Ehrenberg who attributed to them a highly complex organisation, but later
observations negatived these views and showed them to be animals formed
of one or more cells, or colonies of so-called individuals. It is true that this
cell or united protoplasm may show a wonderful amount of differentiation,
what with its nucleus and vacuole, mouth and gullet, its variously-arranged
cilia or flagella, its contractile fibres, its separation into an outer denser and
a more fluid inner protoplasm, and its horny cup and stalks.
Page 575
In these few lines we have a condensed summary of the special qualities of
minute forms of life that afford much interesting work for the microscope.
Fig. 332.—Acineta, magnified 600 diameters (Warne).
Among those widespread, and in some respects heterogeneous, forms of life
associated under the comprehensive title of Infusoria, we encounter types
that not only differ very widely from one another, but which occupy a
different rank or position, so to speak, with regard to the relation they bear
to each other, and also to the outlying representatives of the series—
differences that permeate throughout the ranks of this extensive group.
Furthermore, a considerable number of Infusorial animalcules foreshadow
or typify, in a corresponding degree, the separate or associated cell elements
out of which higher tissue structures—metazoic organisms—are built up.
We may take the well-known example Euglena viridis (Plate III., No. 67),
minute forms of life that afford much interesting work for the microscope.
Fig. 332.—Acineta, magnified 600 diameters (Warne).
Among those widespread, and in some respects heterogeneous, forms of life
associated under the comprehensive title of Infusoria, we encounter types
that not only differ very widely from one another, but which occupy a
different rank or position, so to speak, with regard to the relation they bear
to each other, and also to the outlying representatives of the series—
differences that permeate throughout the ranks of this extensive group.
Furthermore, a considerable number of Infusorial animalcules foreshadow
or typify, in a corresponding degree, the separate or associated cell elements
out of which higher tissue structures—metazoic organisms—are built up.
We may take the well-known example Euglena viridis (Plate III., No. 67),
Page 576
or Paramecium (No. 74), and their allies; these would appear to be the
prototypes of Turbellaria. Another more lowly organised group of the
Ciliata exhibits a distinct and highly-interesting affinity to the Opalinidæ.
There are many other species (Acineta, Plate III., No. 68, for instance),
which at first sight would seem to stand by themselves and present no
marked agreement with any metazoic type. Indeed, the function of these
and other polypites consists simply in seizing food and conveying it through
perforations at the extremity of each separate tentaculum to its interior. In
Acineta certain of the tentacles only are suctorial, and these, being the inner
ones, fulfil the ingestive function, while the peripheral series are prehensile.
This stalked club-shaped body (Fig. 332), which fixes itself to seaweeds or
Bryozoa, is seen to have a nucleus, and also clear vesicles in the body-
substance; its embryos are ciliated. It is an object of considerable interest
even among curious marine animalcules; one or two species inhabit fresh
water. The spiral-mouthed Spirostomum are among the largest of the class,
and in sunlight are visible to the naked eye as slender golden threads of
about 1⁄10th of an inch in length. The mouth slit, extending half the length of
the body, is bordered on one side by cilia. The body is cylindrical and the
surface covered with rows of cilia. Its multiplication takes place by
transverse fission through the middle.
Flagellate Infusoria.—The characteristic of this group, as its name implies,
is the possession of one or more flagella or whip-like appendages, at the
base of which is an opening in the denser surface layer of protoplasm, and
in the interior a nucleus and one or more contractile vacuoles, and not
infrequently a brilliant red spot of pigment known to microscopists as the
eye-spot. The Monads, which constitute the simplest members of the group,
are commonly found in fresh-water pools and vegetable infusions. The
typical form consists simply of a spherical or oval cell provided with a
flagellum. The Volvox was formerly placed in this group, but as it contains
chlorophyll it is properly claimed by the botanist. The collared group
possesses cup-like collars, and these frequently secrete horny receptacles or
cups, and form elegant tree-like colonies.
The mail-coated group are of very varied form, the body being often
prolonged into spiny processes. They have two long flagella which fit into
grooves purposely provided. But the most interesting and remarkable are
prototypes of Turbellaria. Another more lowly organised group of the
Ciliata exhibits a distinct and highly-interesting affinity to the Opalinidæ.
There are many other species (Acineta, Plate III., No. 68, for instance),
which at first sight would seem to stand by themselves and present no
marked agreement with any metazoic type. Indeed, the function of these
and other polypites consists simply in seizing food and conveying it through
perforations at the extremity of each separate tentaculum to its interior. In
Acineta certain of the tentacles only are suctorial, and these, being the inner
ones, fulfil the ingestive function, while the peripheral series are prehensile.
This stalked club-shaped body (Fig. 332), which fixes itself to seaweeds or
Bryozoa, is seen to have a nucleus, and also clear vesicles in the body-
substance; its embryos are ciliated. It is an object of considerable interest
even among curious marine animalcules; one or two species inhabit fresh
water. The spiral-mouthed Spirostomum are among the largest of the class,
and in sunlight are visible to the naked eye as slender golden threads of
about 1⁄10th of an inch in length. The mouth slit, extending half the length of
the body, is bordered on one side by cilia. The body is cylindrical and the
surface covered with rows of cilia. Its multiplication takes place by
transverse fission through the middle.
Flagellate Infusoria.—The characteristic of this group, as its name implies,
is the possession of one or more flagella or whip-like appendages, at the
base of which is an opening in the denser surface layer of protoplasm, and
in the interior a nucleus and one or more contractile vacuoles, and not
infrequently a brilliant red spot of pigment known to microscopists as the
eye-spot. The Monads, which constitute the simplest members of the group,
are commonly found in fresh-water pools and vegetable infusions. The
typical form consists simply of a spherical or oval cell provided with a
flagellum. The Volvox was formerly placed in this group, but as it contains
chlorophyll it is properly claimed by the botanist. The collared group
possesses cup-like collars, and these frequently secrete horny receptacles or
cups, and form elegant tree-like colonies.
The mail-coated group are of very varied form, the body being often
prolonged into spiny processes. They have two long flagella which fit into
grooves purposely provided. But the most interesting and remarkable are
Page 577
the phosphorescent animalcules (Noctiluca), whose beautiful bluish-green
luminosity on the surface of the sea has attracted attention from very early
periods. It was, however, not until the first half of the present century that
the luminosity was discovered to be due to the presence of multitudes of
these minute jelly-like spheres.
Fig. 333.—Noctiluca miliaris;
magnified 150 diameters. Fig. 334.—Pyrocystis; magnified 150 diameters.
The body of the Noctiluca (Fig. 333) is a nearly globular-shaped cyst,
enclosed in a tough membranous wall, from a grooved opening in which a
striated muscular flagellum or proboscis is projected forth, and it is by
means of this the animal swims away even in rough seas. A fine whip-like
flagellum is also located in the same groove. At the apex of the funnel there
is a mass of protoplasm which extends itself as a widely-meshed, highly-
vacuolated network to the inner wall of the cyst, whence it is believed the
phosphorescent light emanates. It multiplies by self-division, first becoming
encysted after withdrawing its flagellum, and then breaking up into
numerous ciliated helmet-shaped swarm spores. Frequently two organisms
fuse into one and then divide into spores.
Noctiluca mainly confines itself to the shallower seas, but there are related
forms met with in the warmer open seas; these belong to the genus
Pyrocystis (Fig. 334). In one variety the body is perfectly spherical and
without the big flagellum or proboscis. Professor Butschli, however, regards
luminosity on the surface of the sea has attracted attention from very early
periods. It was, however, not until the first half of the present century that
the luminosity was discovered to be due to the presence of multitudes of
these minute jelly-like spheres.
Fig. 333.—Noctiluca miliaris;
magnified 150 diameters. Fig. 334.—Pyrocystis; magnified 150 diameters.
The body of the Noctiluca (Fig. 333) is a nearly globular-shaped cyst,
enclosed in a tough membranous wall, from a grooved opening in which a
striated muscular flagellum or proboscis is projected forth, and it is by
means of this the animal swims away even in rough seas. A fine whip-like
flagellum is also located in the same groove. At the apex of the funnel there
is a mass of protoplasm which extends itself as a widely-meshed, highly-
vacuolated network to the inner wall of the cyst, whence it is believed the
phosphorescent light emanates. It multiplies by self-division, first becoming
encysted after withdrawing its flagellum, and then breaking up into
numerous ciliated helmet-shaped swarm spores. Frequently two organisms
fuse into one and then divide into spores.
Noctiluca mainly confines itself to the shallower seas, but there are related
forms met with in the warmer open seas; these belong to the genus
Pyrocystis (Fig. 334). In one variety the body is perfectly spherical and
without the big flagellum or proboscis. Professor Butschli, however, regards
Page 578
this species as an encysted or resting phase of the commoner and better-
known form.
The late Mr. Philip Gosse, F.R.S., was the first microscopist to describe the
Noctiluca. After careful observation, he wrote in his “Naturalist’s Rambles”
as follows:—“I had an opportunity of becoming acquainted with the minute
animals to which a great portion of the luminousness of the sea is attributed.
One of my large glass vases of sea-water I had observed to become
suddenly at night, when tapped with the finger, studded with minute but
brilliant sparks at various points on the surface of the water. I set the jar in
the window, and was not long in discovering, without the aid of a lens, a
goodly number of the tiny jelly-like globules of Noctiluca miliaris
swimming about in various directions. They swam with an even gliding
motion, much resembling that of the Volvox globator of our fresh-water
pools. They congregated in little groups, and a shake of the vessel sent them
darting down from the surface. It was not easy to keep them in view when
seen, owing rather to their extreme delicacy and colourless transparency
than to their minuteness. They were, in fact, distinctly appreciable by the
naked eye, measuring from 1⁄50th to 1⁄30th of an inch in diameter.”
Among the numerous fresh-water members of the flagellate infusoria, there
is one which especially calls for notice, Codosiga, discovered by the late
Professor H. J. Clark. This minute body bears a delicate funnel-shaped
protoplasmic expansion or collar, common to the several members of this
organic series. The flagellum is placed at the base of the oral opening, and
within the circumscribed area of the collar, which is of such extreme tenuity
that its true form and nature can only be determined by a very careful
adjustment of the achromatic condenser and accessory apparatus employed,
together with a wide-angled objective. It is seen to greater advantage by
supplying the animal with very fine particles of colouring matter. In this
way it is found that the infundibuliform cup consists of protoplasm, through
which the flagellum is protruded and withdrawn into the general substance
of the Monad’s body (Fig. 335). As many as twenty or more zooids are
attached to the extremity of a slender footstalk. The length of the body,
exclusive of the collar, is 1⁄2500th to the 1⁄1200th of an inch. The habitat of these
bodies is fresh water. Mr. Saville Kent in 1869 discovered some of these
interesting infusoria in the London Docks.
known form.
The late Mr. Philip Gosse, F.R.S., was the first microscopist to describe the
Noctiluca. After careful observation, he wrote in his “Naturalist’s Rambles”
as follows:—“I had an opportunity of becoming acquainted with the minute
animals to which a great portion of the luminousness of the sea is attributed.
One of my large glass vases of sea-water I had observed to become
suddenly at night, when tapped with the finger, studded with minute but
brilliant sparks at various points on the surface of the water. I set the jar in
the window, and was not long in discovering, without the aid of a lens, a
goodly number of the tiny jelly-like globules of Noctiluca miliaris
swimming about in various directions. They swam with an even gliding
motion, much resembling that of the Volvox globator of our fresh-water
pools. They congregated in little groups, and a shake of the vessel sent them
darting down from the surface. It was not easy to keep them in view when
seen, owing rather to their extreme delicacy and colourless transparency
than to their minuteness. They were, in fact, distinctly appreciable by the
naked eye, measuring from 1⁄50th to 1⁄30th of an inch in diameter.”
Among the numerous fresh-water members of the flagellate infusoria, there
is one which especially calls for notice, Codosiga, discovered by the late
Professor H. J. Clark. This minute body bears a delicate funnel-shaped
protoplasmic expansion or collar, common to the several members of this
organic series. The flagellum is placed at the base of the oral opening, and
within the circumscribed area of the collar, which is of such extreme tenuity
that its true form and nature can only be determined by a very careful
adjustment of the achromatic condenser and accessory apparatus employed,
together with a wide-angled objective. It is seen to greater advantage by
supplying the animal with very fine particles of colouring matter. In this
way it is found that the infundibuliform cup consists of protoplasm, through
which the flagellum is protruded and withdrawn into the general substance
of the Monad’s body (Fig. 335). As many as twenty or more zooids are
attached to the extremity of a slender footstalk. The length of the body,
exclusive of the collar, is 1⁄2500th to the 1⁄1200th of an inch. The habitat of these
bodies is fresh water. Mr. Saville Kent in 1869 discovered some of these
interesting infusoria in the London Docks.
Page 579
“The more exact significance of the special organ, the collar, is manifest by
the circulatory currents or cyclosis induced, and there can be no room for
doubt that this structure finds its precise homologue in the pseudopodia of
the foraminiferous group of the Rhizopoda, in which a similar circulation or
cyclosis of the constituent sarcode is exhibited. The whole of this highly-
interesting flagellate order, a comparatively small one as yet, are
remarkable for their pale glaucous green or florescent hue, such colour
assisting materially in their recognition, even when the magnifying power
employed is insufficient for the detection of the very characteristic collar
with its enclosed flagellum.”66
the circulatory currents or cyclosis induced, and there can be no room for
doubt that this structure finds its precise homologue in the pseudopodia of
the foraminiferous group of the Rhizopoda, in which a similar circulation or
cyclosis of the constituent sarcode is exhibited. The whole of this highly-
interesting flagellate order, a comparatively small one as yet, are
remarkable for their pale glaucous green or florescent hue, such colour
assisting materially in their recognition, even when the magnifying power
employed is insufficient for the detection of the very characteristic collar
with its enclosed flagellum.”66
Page 580
Fig. 335.—Codosiga umbellata; a few colonies of Zooids diverging from the
parent foot-stalk with flagella extended, magnified 650 diameters.
Ciliata.—Types of Ciliata obtained from hay infusions are very numerous.
Ehrenberg’s animalcules were mainly of a large size, and of those belonging
to the higher order of the Ciliata, pertaining to such genera as Paramecium,
Colpoda, Cyclidium, Oxytricha, and Vorticella. These, however, represent
but an insignificant minority of the hosts of flagellate forms which abound
in our humid climate, and in hay infusions in particular. In such infusions,
watched from day to day and produced from hay obtained from different
localities, the number of types developed in regular sequence is found to be
perfectly marvellous, commencing with the Monas proper, Amphimonas
and Heteromita; while Bacteria, in their motile and quiescent forms, are
invariably present and furnish an abundant supply of material for the
microscope.67
parent foot-stalk with flagella extended, magnified 650 diameters.
Ciliata.—Types of Ciliata obtained from hay infusions are very numerous.
Ehrenberg’s animalcules were mainly of a large size, and of those belonging
to the higher order of the Ciliata, pertaining to such genera as Paramecium,
Colpoda, Cyclidium, Oxytricha, and Vorticella. These, however, represent
but an insignificant minority of the hosts of flagellate forms which abound
in our humid climate, and in hay infusions in particular. In such infusions,
watched from day to day and produced from hay obtained from different
localities, the number of types developed in regular sequence is found to be
perfectly marvellous, commencing with the Monas proper, Amphimonas
and Heteromita; while Bacteria, in their motile and quiescent forms, are
invariably present and furnish an abundant supply of material for the
microscope.67
Page 581
Vorticellidæ constitute one of the most numerous families of the ciliate
infusoria. All its members are at once recognised by their normal stationary
condition, and by the structure of their oral system. In but few of the genera
is there any marked divergence from this formula, and when any exists it is
made manifest by an increase in development of some one of its elements at
the expense of another. For instance, in the genus Spirochona, the external
edge of the encircling border or peristome is suppressed, while the inner
portion is abnormally developed into a transparent and highly elevated
spiral membrane. The bell-animalcules usually possess stalks, and are either
solitary or form branching colonies. Conichilus vorticella (Plate III., No.
80) is a well-known member of the colony stock, all the zooids of which are
united on a slender branching pedicle, which consists of a central
contractile cord enclosed within a tubular hyaline sheath. There are many
other shrub-like colonies all variously modified in form and character. The
Epistylis opercularia, or nodding-bell animalcule, is an interesting member
of a numerous host of solitary short-stalked forms (Fig. 337). When the
animal is disturbed, the heads drop down towards the stalk. This animalcule
has been found to form a colony; and another, Carchesium, whose tiny
branched tree-like colonies resemble little white globular masses of moulds,
are seen at once to drop down towards the base of the colony with a jerky
movement if the cell be touched. By a process of encysting, all the
Vorticellæ and many of the more highly-organised ciliata have the means of
what may be termed self-preservation. Should the water dry up in which
they have been living, the little animal encases itself in mud at the bottom
of the pool. Should this be baked by the sun not the least injury arises, for at
this stage it crumbles into dust, and is carried by the wind to long distances,
but the first shower of rain calls it back to active life, and soon after it is
seen to issue forth as a free swimming bud.
Thuricola valvata (Plate III., No. 72) possesses a hinge-like process which
closes up like a door when the animal contracts itself into its case. This very
effectually protects it from assault. Both portions of the valve are capable of
extension. Another group of ciliate infusoria also possess a limited number
of cilia, but these, although restricted to the under surface of their bodies,
have an unrestricted range of motion. The group are all free swimmers,
belonging to the genus Oxytricha. They possess two separate alimentary
orifices, neither of which are situated at the extremities or encased by a
infusoria. All its members are at once recognised by their normal stationary
condition, and by the structure of their oral system. In but few of the genera
is there any marked divergence from this formula, and when any exists it is
made manifest by an increase in development of some one of its elements at
the expense of another. For instance, in the genus Spirochona, the external
edge of the encircling border or peristome is suppressed, while the inner
portion is abnormally developed into a transparent and highly elevated
spiral membrane. The bell-animalcules usually possess stalks, and are either
solitary or form branching colonies. Conichilus vorticella (Plate III., No.
80) is a well-known member of the colony stock, all the zooids of which are
united on a slender branching pedicle, which consists of a central
contractile cord enclosed within a tubular hyaline sheath. There are many
other shrub-like colonies all variously modified in form and character. The
Epistylis opercularia, or nodding-bell animalcule, is an interesting member
of a numerous host of solitary short-stalked forms (Fig. 337). When the
animal is disturbed, the heads drop down towards the stalk. This animalcule
has been found to form a colony; and another, Carchesium, whose tiny
branched tree-like colonies resemble little white globular masses of moulds,
are seen at once to drop down towards the base of the colony with a jerky
movement if the cell be touched. By a process of encysting, all the
Vorticellæ and many of the more highly-organised ciliata have the means of
what may be termed self-preservation. Should the water dry up in which
they have been living, the little animal encases itself in mud at the bottom
of the pool. Should this be baked by the sun not the least injury arises, for at
this stage it crumbles into dust, and is carried by the wind to long distances,
but the first shower of rain calls it back to active life, and soon after it is
seen to issue forth as a free swimming bud.
Thuricola valvata (Plate III., No. 72) possesses a hinge-like process which
closes up like a door when the animal contracts itself into its case. This very
effectually protects it from assault. Both portions of the valve are capable of
extension. Another group of ciliate infusoria also possess a limited number
of cilia, but these, although restricted to the under surface of their bodies,
have an unrestricted range of motion. The group are all free swimmers,
belonging to the genus Oxytricha. They possess two separate alimentary
orifices, neither of which are situated at the extremities or encased by a
Page 582
dense integument. Their locomotive organs
consist either of setæ, vibratile cilia, or non-
vibratile styles or uncini, variously situated, and
all serving to make these infusorial animals very
active (Plate III., Nos. 73 and 77). A typical
species is the mussel-animalcule (Stylonychia,
Fig. 338), common in all infusions and pools of
water. Its body is oval and flattened, and about
1⁄100th of an inch in length. At one end a funnel-
shaped depression or mouth, with a ciliated
margin, leads to the inner part of the body, in
Fig. 336.—Vorticella microstoma. which are two oval bodies, a nucleus and a
contractile vacuole, which is seen to contract
rhythmically. The creature can also stalk along by means of its cilia or setæ,
and set up currents to the mouth. Plate III., Nos. 70, 71, 72, 73, and 74, are
types of these interesting bodies.
consist either of setæ, vibratile cilia, or non-
vibratile styles or uncini, variously situated, and
all serving to make these infusorial animals very
active (Plate III., Nos. 73 and 77). A typical
species is the mussel-animalcule (Stylonychia,
Fig. 338), common in all infusions and pools of
water. Its body is oval and flattened, and about
1⁄100th of an inch in length. At one end a funnel-
shaped depression or mouth, with a ciliated
margin, leads to the inner part of the body, in
Fig. 336.—Vorticella microstoma. which are two oval bodies, a nucleus and a
contractile vacuole, which is seen to contract
rhythmically. The creature can also stalk along by means of its cilia or setæ,
and set up currents to the mouth. Plate III., Nos. 70, 71, 72, 73, and 74, are
types of these interesting bodies.
Page 583
Fig. 337.—Nodding-bell Fig. 338.—Mussel-animalcule (Stylonychia mytilus) under
animalcule (Epistyles surface.
operculata) × 250 a. Mouth; b. Contractile vacuole; c. Nucleus. (Magnified
(Warne). 150 diameters.
Dr. Balbini believes a true sexual generation occurs among these organisms,
but, with the exception of the Paramecium, this has not been seen to take
place; even Gruber’s more recent investigations appear to be inconclusive
on this point. Conjugation, however, it is said takes place among some
attached forms, as in the Stentors. These have been seen to put forth a bud
from the body base, and soon after become free swimming bodies. The
trumpet-animalcule (Stentor), a conspicuous member of the ciliata, is
comparatively large, being about the 1⁄25th of an inch in length when
extended to the full size. It is usually found attached to the under sides of
duckweed, and is continually changing its form from that of a small knob
when contracted, to the trumpet shape seen in Fig. 339, No. 6, when fully
extended, and from which it derives its name. The long cilia projected from
animalcule (Epistyles surface.
operculata) × 250 a. Mouth; b. Contractile vacuole; c. Nucleus. (Magnified
(Warne). 150 diameters.
Dr. Balbini believes a true sexual generation occurs among these organisms,
but, with the exception of the Paramecium, this has not been seen to take
place; even Gruber’s more recent investigations appear to be inconclusive
on this point. Conjugation, however, it is said takes place among some
attached forms, as in the Stentors. These have been seen to put forth a bud
from the body base, and soon after become free swimming bodies. The
trumpet-animalcule (Stentor), a conspicuous member of the ciliata, is
comparatively large, being about the 1⁄25th of an inch in length when
extended to the full size. It is usually found attached to the under sides of
duckweed, and is continually changing its form from that of a small knob
when contracted, to the trumpet shape seen in Fig. 339, No. 6, when fully
extended, and from which it derives its name. The long cilia projected from
Page 584
the upper part form a spiral within the margin of the open mouth leading to
the digestive sac. A contractile vacuole lies to the right of the oral opening.
New individuals are produced by the process of budding, and in the form of
ciliated embryos from the nucleus. Stentors are commonly met with in fresh
water, and are usually of a brilliant green colour. These little bodies will
bear cutting up: if only a fragment of the nucleus be included in the section,
the injury is soon repaired.
Rotifera, or Wheel-animalcules (Fig. 339).—In this group we have a higher
type of animal, with a more complex organisation than those previously
noticed. The great majority inhabit fresh water, and are readily developed in
hay infusions, in bog-moss, in house-top gutters, everywhere if looked for
after a shower of rain. The rotating organs from which these fascinating
animalcula derive their name consist of two disc-like bodies whose margins
are fringed with rows of cilia, which create currents toward the oral
aperture, and which have given rise to the optical delusion of rotating
wheels. The disposition of the cilia is so arranged as to bring food to the
rotifer and conduct it to the mastax or digesting apparatus—a muscular bulb
moved by a series of muscles—the gastric glands and stomach. The great
transparency of the whole structure permits of the animal economy being
easily studied. The body is covered with a horny envelope of two layers,
and is divided into segmental divisions, which slide into each other
telescopic fashion. Consequently, as the water dries up, the animal is for a
long time rendered indestructible and capable of resisting varying
temperatures and the action of caustic reagents.
Rotifers are oviparous, and their eggs are conspicuous and of three kinds.
The common soft-shelled eggs produce females, the smaller and more
spherical produce males. The ephippial, or summer eggs, are often beset
with spines or bosses; these have only a membranous covering, and are
hatched soon after they are laid, or before leaving the ova sac. The male
rotifer is but a third of the length of the female, often without cilia, and
appears to have no alimentary tract; indeed, the only internal organ is a
large sperm sac. Rotifers have been divided by Dr. Hudson and the late Mr.
Gosse in their charming work on these very interesting “Wheel-
animalcules” into four orders, according to their powers of locomotion, as
follows:—(1) Rhizota, the rooted; (2) Bdelloida, the leech-like, that swim
the digestive sac. A contractile vacuole lies to the right of the oral opening.
New individuals are produced by the process of budding, and in the form of
ciliated embryos from the nucleus. Stentors are commonly met with in fresh
water, and are usually of a brilliant green colour. These little bodies will
bear cutting up: if only a fragment of the nucleus be included in the section,
the injury is soon repaired.
Rotifera, or Wheel-animalcules (Fig. 339).—In this group we have a higher
type of animal, with a more complex organisation than those previously
noticed. The great majority inhabit fresh water, and are readily developed in
hay infusions, in bog-moss, in house-top gutters, everywhere if looked for
after a shower of rain. The rotating organs from which these fascinating
animalcula derive their name consist of two disc-like bodies whose margins
are fringed with rows of cilia, which create currents toward the oral
aperture, and which have given rise to the optical delusion of rotating
wheels. The disposition of the cilia is so arranged as to bring food to the
rotifer and conduct it to the mastax or digesting apparatus—a muscular bulb
moved by a series of muscles—the gastric glands and stomach. The great
transparency of the whole structure permits of the animal economy being
easily studied. The body is covered with a horny envelope of two layers,
and is divided into segmental divisions, which slide into each other
telescopic fashion. Consequently, as the water dries up, the animal is for a
long time rendered indestructible and capable of resisting varying
temperatures and the action of caustic reagents.
Rotifers are oviparous, and their eggs are conspicuous and of three kinds.
The common soft-shelled eggs produce females, the smaller and more
spherical produce males. The ephippial, or summer eggs, are often beset
with spines or bosses; these have only a membranous covering, and are
hatched soon after they are laid, or before leaving the ova sac. The male
rotifer is but a third of the length of the female, often without cilia, and
appears to have no alimentary tract; indeed, the only internal organ is a
large sperm sac. Rotifers have been divided by Dr. Hudson and the late Mr.
Gosse in their charming work on these very interesting “Wheel-
animalcules” into four orders, according to their powers of locomotion, as
follows:—(1) Rhizota, the rooted; (2) Bdelloida, the leech-like, that swim
Page 585
and creep like a leech; (3) Ploïma, the sea-worthy, that only swim with their
ciliary wreath; (4) Scirtopoda, the skippers, that swim with their cilia and
skip with arthropodous limbs. These, again, are subdivided into families.
With such hardy creatures as Philodina, Adineta, Brachionus, &c., creatures
to whom extremes of cold, heat, and drought are the ordinary conditions of
life, nothing can be easier to keep going throughout the year. Mr. C. F.
Rousselet, who has so thoroughly succeeded in mounting Rotifers with their
cilia fully extended, recently exhibited at one of the evening meetings of the
Royal Microscopical Society, London, no less than four hundred specimens
in a natural and perfect condition, the nervous system being seen more
clearly from its successful staining throughout the body than in the living
rotifer.
Fig. 339.
1. Rotifer vulgaris with its cilia; b. rotating; c. horn; d. œsophagus; f. outer case; g.
ova, foot protruding through outer case. 2. Same in the contracted state and at rest,
showing the segmentation of the body and development of young. 3. Pitcher-
shaped Brachionus, furnished with two horny projections; a. mastax; b. shell; c.
cilia, rotating disc; d. foot. 4. Baker’s Brachionus, with six horny setæ; these are
ciliary wreath; (4) Scirtopoda, the skippers, that swim with their cilia and
skip with arthropodous limbs. These, again, are subdivided into families.
With such hardy creatures as Philodina, Adineta, Brachionus, &c., creatures
to whom extremes of cold, heat, and drought are the ordinary conditions of
life, nothing can be easier to keep going throughout the year. Mr. C. F.
Rousselet, who has so thoroughly succeeded in mounting Rotifers with their
cilia fully extended, recently exhibited at one of the evening meetings of the
Royal Microscopical Society, London, no less than four hundred specimens
in a natural and perfect condition, the nervous system being seen more
clearly from its successful staining throughout the body than in the living
rotifer.
Fig. 339.
1. Rotifer vulgaris with its cilia; b. rotating; c. horn; d. œsophagus; f. outer case; g.
ova, foot protruding through outer case. 2. Same in the contracted state and at rest,
showing the segmentation of the body and development of young. 3. Pitcher-
shaped Brachionus, furnished with two horny projections; a. mastax; b. shell; c.
cilia, rotating disc; d. foot. 4. Baker’s Brachionus, with six horny setæ; these are
Page 586
retracted when the cilia are in action; the letters relate to the same internal organs
as in the former; the ova sac seen filled with eggs. 5 and 6. B. ovalis, closed, and
with cilia displayed.
There is also a family of Rotatoria with a single rotatory organ, disposed
around the margin of the case. This comprises at present a very small group.
The Œcistes is a member of the family (Plate III., No. 69). A single ciliary
wreath leads to the alimentary canal, and a pharyngeal bulb or mastax
comprises the apparatus of nutrition. The visual organs are red, as in other
rotifers, and the ovarium contains several ova, shown in No. 69. The
envelope is a gelatinous transparent sheath, into which the animalcule can
withdraw itself, its attachment to the bottom being by the end of the foot-
like tail. The most interesting among this genus are the Floscularians. These
creatures may undoubtedly be described as among the most beautiful and
interesting of infusorial animals.
The Stephanoceros, “crowned animalcule,” as it is termed, is about 1⁄36th of
an inch in length, and enclosed in a transparent cylindrical flexible case,
beyond which it protrudes five long arms in a graceful manner. These,
touching at their points, give a form from which it derives its name. These
arms are furnished with several rows of short cilia, which seize the food
brought within their grasp until it can be swallowed. In addition to the
rotatory organs, they have short flexible processes, or cornu, attached to the
outside of one or more of their lobes. The water vascular system consists of
two canals arising from a small pyriform contractile vesicle, situated below
the stomach. The ova, after leaving the ova sac, remain quiescent until their
cilia are developed. Floscularians, like Melicertans, have a certain affinity
in form with Vorticellians and Stentors, and also with Campanulariæ,
among polypes. Their cilia are less regular when in action than in other
Rotatoria. When they retreat into their transparent cells they appear to fold
themselves up. Their internal structure can be seen through the external
case, and ova are observed enclosed in an ova sac; when thrown off they
remain quiescent until the formation of their cilia. The whole family furnish
interesting objects for microscopic investigation.
Melicerta ringens (“beaded Melicerta”).—Of all the Melicerta, or “horny
floscularia,” this is the most beautiful. Its crystalline body is enclosed in a
pellucid covering, wider at the top than the bottom, of a dark yellow or
as in the former; the ova sac seen filled with eggs. 5 and 6. B. ovalis, closed, and
with cilia displayed.
There is also a family of Rotatoria with a single rotatory organ, disposed
around the margin of the case. This comprises at present a very small group.
The Œcistes is a member of the family (Plate III., No. 69). A single ciliary
wreath leads to the alimentary canal, and a pharyngeal bulb or mastax
comprises the apparatus of nutrition. The visual organs are red, as in other
rotifers, and the ovarium contains several ova, shown in No. 69. The
envelope is a gelatinous transparent sheath, into which the animalcule can
withdraw itself, its attachment to the bottom being by the end of the foot-
like tail. The most interesting among this genus are the Floscularians. These
creatures may undoubtedly be described as among the most beautiful and
interesting of infusorial animals.
The Stephanoceros, “crowned animalcule,” as it is termed, is about 1⁄36th of
an inch in length, and enclosed in a transparent cylindrical flexible case,
beyond which it protrudes five long arms in a graceful manner. These,
touching at their points, give a form from which it derives its name. These
arms are furnished with several rows of short cilia, which seize the food
brought within their grasp until it can be swallowed. In addition to the
rotatory organs, they have short flexible processes, or cornu, attached to the
outside of one or more of their lobes. The water vascular system consists of
two canals arising from a small pyriform contractile vesicle, situated below
the stomach. The ova, after leaving the ova sac, remain quiescent until their
cilia are developed. Floscularians, like Melicertans, have a certain affinity
in form with Vorticellians and Stentors, and also with Campanulariæ,
among polypes. Their cilia are less regular when in action than in other
Rotatoria. When they retreat into their transparent cells they appear to fold
themselves up. Their internal structure can be seen through the external
case, and ova are observed enclosed in an ova sac; when thrown off they
remain quiescent until the formation of their cilia. The whole family furnish
interesting objects for microscopic investigation.
Melicerta ringens (“beaded Melicerta”).—Of all the Melicerta, or “horny
floscularia,” this is the most beautiful. Its crystalline body is enclosed in a
pellucid covering, wider at the top than the bottom, of a dark yellow or
Page 587
reddish-brown colour, which gradually becomes encrusted by zones of a
variety of shapes, cemented together with a peculiar secretion that hardens
in water. It derives its name from these pellets, which have the appearance
of rows of beads. Mr. Gosse furnished an excellent account of the
architectural instincts of Melicerta ringens: “An animalcule so minute as to
be with difficulty appreciable by the naked eye, inhabiting a tube composed
of pellets, which it forms and lays one by one. It is a mason who not only
builds up his mansion brick by brick, but makes his bricks as he goes on,
from substances which he collects around him, shaping them in a mould
which he carries on his body.
“The pellets composing the case are very regularly placed in position; in a
fine specimen, about the 1⁄30th of an inch in length, when fully expanded, as
many as fifteen longitudinal rows of pellets were counted, which gave
about thirty-two rows in all. As it exposes itself more and more, suddenly
two large rounded discs are expanded, around which, at the same instant, a
wreath of cilia is seen performing surprising motions.
“On mixing carmine with the water, the course of the ciliary current is
readily traced, and forms a fine spectacle. The particles are hurled round the
margin of the disc, until they pass off in front through the great sinus,
between the larger petals. If the pigment be abundant, the cloudy torrent for
the most part rushes off, and prevents our seeing what takes place; but if the
atoms be few, we see them swiftly glide along the facial surface, following
the irregularities of outline with beautiful precision, dash round the
projecting chin like a fleet of boats doubling a bold headland, and lodge
themselves, one after another, in the little cup-like receptacle beneath. Mr.
Gosse, believing that the pellets of the case might be prepared in the cup-
like receptacle, watched the animal, and presently had the satisfaction of
seeing it bend its head forward, as anticipated, and after a second or two
raise it again; the little cup having in the meantime lost its contents. It
immediately began to fill again; and when it was full, and the contents were
consolidated by rotation, aided probably by the admixture of a salivary
secretion, it was again bent down to the margin of the case, and emptied of
its pellet. This process he saw repeated many times in succession, until a
goodly array of dark-red pellets were laid upon the yellowish-brown ones,
but very irregularly. After a certain number were deposited in one part, the
variety of shapes, cemented together with a peculiar secretion that hardens
in water. It derives its name from these pellets, which have the appearance
of rows of beads. Mr. Gosse furnished an excellent account of the
architectural instincts of Melicerta ringens: “An animalcule so minute as to
be with difficulty appreciable by the naked eye, inhabiting a tube composed
of pellets, which it forms and lays one by one. It is a mason who not only
builds up his mansion brick by brick, but makes his bricks as he goes on,
from substances which he collects around him, shaping them in a mould
which he carries on his body.
“The pellets composing the case are very regularly placed in position; in a
fine specimen, about the 1⁄30th of an inch in length, when fully expanded, as
many as fifteen longitudinal rows of pellets were counted, which gave
about thirty-two rows in all. As it exposes itself more and more, suddenly
two large rounded discs are expanded, around which, at the same instant, a
wreath of cilia is seen performing surprising motions.
“On mixing carmine with the water, the course of the ciliary current is
readily traced, and forms a fine spectacle. The particles are hurled round the
margin of the disc, until they pass off in front through the great sinus,
between the larger petals. If the pigment be abundant, the cloudy torrent for
the most part rushes off, and prevents our seeing what takes place; but if the
atoms be few, we see them swiftly glide along the facial surface, following
the irregularities of outline with beautiful precision, dash round the
projecting chin like a fleet of boats doubling a bold headland, and lodge
themselves, one after another, in the little cup-like receptacle beneath. Mr.
Gosse, believing that the pellets of the case might be prepared in the cup-
like receptacle, watched the animal, and presently had the satisfaction of
seeing it bend its head forward, as anticipated, and after a second or two
raise it again; the little cup having in the meantime lost its contents. It
immediately began to fill again; and when it was full, and the contents were
consolidated by rotation, aided probably by the admixture of a salivary
secretion, it was again bent down to the margin of the case, and emptied of
its pellet. This process he saw repeated many times in succession, until a
goodly array of dark-red pellets were laid upon the yellowish-brown ones,
but very irregularly. After a certain number were deposited in one part, the
Page 588
animal would suddenly turn itself round in its case, and deposit some in
another part. It took from two-and-a-half to three-and-a-half minutes to
make and deposit a pellet.”
Melicerta may be found in clear pools, mill-ponds, and other places through
which a current of water gently flows. If a portion of water-weed be brought
home and placed in a small glass zoophyte-trough, and carefully examined
with a magnifying power of about fifty diameters, a few delicate-looking
projections of a reddish-brown colour will probably be seen adhering to the
plant; these are the tubular cases of Melicerta, which, after a short period of
rest, will be seen to be animals of 1⁄12th of an inch or more in length.
Porifera. Spongiadæ.
Sponges.—The term Porifera, or
“canal-bearing zoophytes,” was
applied by the late Dr. Grant to
designate the remarkable class of
organisms known as sponges, met
with in every sea, and numbering
about two thousand species, varying
in size from a pin’s head to masses
several feet in height; and weighing
from a few grains to over a hundred
Fig. 340.—Spongia panicea.
pounds. Sponges assume an endless
variety of shapes, as cups, vases,
Bread-crumb Sponge, showing currents entering spheres, tubes, baskets, branched-
surface a, and leaving by oscules b.
like trees, but often as shapeless
masses. When living they are all
colours and all consistences, soft and gelatinous, fleshy, leathery or stony. A
fuller knowledge of sponges was gained in 1825, when Dr. Robert Grant
examined a fragment of living sponge under the microscope. On bringing it
to the side of the glass cell in which he had preserved it, he beheld this
living fountain pouring forth a torrent of liquid matter in rapid succession,
and he was at once convinced that a current flowed out of the larger
orifices. He introduced a small portion of fine chalk, and saw particles
another part. It took from two-and-a-half to three-and-a-half minutes to
make and deposit a pellet.”
Melicerta may be found in clear pools, mill-ponds, and other places through
which a current of water gently flows. If a portion of water-weed be brought
home and placed in a small glass zoophyte-trough, and carefully examined
with a magnifying power of about fifty diameters, a few delicate-looking
projections of a reddish-brown colour will probably be seen adhering to the
plant; these are the tubular cases of Melicerta, which, after a short period of
rest, will be seen to be animals of 1⁄12th of an inch or more in length.
Porifera. Spongiadæ.
Sponges.—The term Porifera, or
“canal-bearing zoophytes,” was
applied by the late Dr. Grant to
designate the remarkable class of
organisms known as sponges, met
with in every sea, and numbering
about two thousand species, varying
in size from a pin’s head to masses
several feet in height; and weighing
from a few grains to over a hundred
Fig. 340.—Spongia panicea.
pounds. Sponges assume an endless
variety of shapes, as cups, vases,
Bread-crumb Sponge, showing currents entering spheres, tubes, baskets, branched-
surface a, and leaving by oscules b.
like trees, but often as shapeless
masses. When living they are all
colours and all consistences, soft and gelatinous, fleshy, leathery or stony. A
fuller knowledge of sponges was gained in 1825, when Dr. Robert Grant
examined a fragment of living sponge under the microscope. On bringing it
to the side of the glass cell in which he had preserved it, he beheld this
living fountain pouring forth a torrent of liquid matter in rapid succession,
and he was at once convinced that a current flowed out of the larger
orifices. He introduced a small portion of fine chalk, and saw particles
Page 589
driven into the interior, and pass out again by different ways. To determine
the cause of the currents, it was necessary to make a closer examination of
the anatomy of the sponge. For this purpose he cut or peeled off thin
sections, and saw that the whole substance was divided into flagellated
chambers, enclosing spherical and other bodies, and perforated by pores.
Each chamber proved to be about 1⁄500th of an inch in diameter, groups of
them opening by a wider orifice into a common space, or canaliculus, and
joining others to form canals terminating in larger oscular canals. The walls
throughout are lined with flat cells, but in the flagellated chambers the
living cells are more or less cylindrical, and each is provided at the free end
with a whip-like appendage, or flagellum. Furthermore the upper margin
was seen to be expanded into a thin hyaline collar, so that the whip
appeared to have its origin in the centre of a basin or funnel. The currents of
water traversing the body of the sponge are kept up by the movements of
the flagella of the collar-cells. These beat the water in the flagellated
chambers into the rootlets of the canals leading to the oscules. To replace
this, water flows into the flagellated chambers from the rootlets of the
canals passing down from the groups of pores in the skin. The currents
entering the sponge bring in oxygenated sea-water and minute food
particles, such as diatoms and infusorial organisms; the currents from the
oscules contain an excess of carbonic acid of waste products, resulting from
vital activity and indigestible remains. The cells lining the canals effect the
exchange of gases, and take up food particles.
Professor Grant’s careful and
instructive researches were begun
on the smaller kind of British
sponges hanging down from
rocks (Spongia coalita), and on
which he gazed for “twenty-five
minutes, until obliged to
withdraw his eyes from fatigue.”
This sponge fixes itself by a root;
and the currents enter through the
stem and body, and leave
principally by oscules placed on Fig. 341.—A section of a flagellate chamber of a
Fresh-water Sponge, showing collar-cells
the branches. (Vosmaer).
the cause of the currents, it was necessary to make a closer examination of
the anatomy of the sponge. For this purpose he cut or peeled off thin
sections, and saw that the whole substance was divided into flagellated
chambers, enclosing spherical and other bodies, and perforated by pores.
Each chamber proved to be about 1⁄500th of an inch in diameter, groups of
them opening by a wider orifice into a common space, or canaliculus, and
joining others to form canals terminating in larger oscular canals. The walls
throughout are lined with flat cells, but in the flagellated chambers the
living cells are more or less cylindrical, and each is provided at the free end
with a whip-like appendage, or flagellum. Furthermore the upper margin
was seen to be expanded into a thin hyaline collar, so that the whip
appeared to have its origin in the centre of a basin or funnel. The currents of
water traversing the body of the sponge are kept up by the movements of
the flagella of the collar-cells. These beat the water in the flagellated
chambers into the rootlets of the canals leading to the oscules. To replace
this, water flows into the flagellated chambers from the rootlets of the
canals passing down from the groups of pores in the skin. The currents
entering the sponge bring in oxygenated sea-water and minute food
particles, such as diatoms and infusorial organisms; the currents from the
oscules contain an excess of carbonic acid of waste products, resulting from
vital activity and indigestible remains. The cells lining the canals effect the
exchange of gases, and take up food particles.
Professor Grant’s careful and
instructive researches were begun
on the smaller kind of British
sponges hanging down from
rocks (Spongia coalita), and on
which he gazed for “twenty-five
minutes, until obliged to
withdraw his eyes from fatigue.”
This sponge fixes itself by a root;
and the currents enter through the
stem and body, and leave
principally by oscules placed on Fig. 341.—A section of a flagellate chamber of a
Fresh-water Sponge, showing collar-cells
the branches. (Vosmaer).
Page 590
At present too little is known as to
the physiology of digestion in
sponges to permit of a definite
statement on the subject. In
specimens fed upon carmine the
collar-cells have been found loaded
with granules; in others, again, the
flat cells lining the subdermal
cavities have been found gorged with
colour granules. From Bowerbank’s
monograph on the British Spongiadæ
Fig. 342.—An Ascon Sponge.
(1864 and 1874) nothing of
importance can be gained on the
A. Magnified × 20 diameters; B. × 80 diameters; subject; in fact, it relates almost
C. Transverse section; D. Collar-cells, × 700
diameters. The embryo, an extremely minute oval entirely to the structure and
cyst, is furnished with a flagellum for swimming; organisation of sponges in their dried
in the third it assumes an amœboid form (Warne.) or preserved condition, and therefore
is only of value for purposes of
specific identification. One of the simplest of living sponges, the
microscopic structure of which it is possible to trace, Ascetta primordialis,
is found on seaweeds in the Mediterranean. In its simple unbranched
condition it forms a minute white sac about one twenty-fifth of an inch in
height, opening above by a wide round oscule and narrowing below to a
stalk (Fig. 342). The walls are very thin and perforated by pores, through
which the water passes into the interior. The walls of the sac are composed
of two layers, an inner lining of collar-cells, and an outer layer consisting of
a gelatinous matrix containing amœboid bodies and transparent three-rayed
spicules. These serve to support the walls and as a frame-work for the
pores, as in all the sponges. By eliminating the spicular skeleton, and by
supposing the tube to be more globular, the “olynthus form” will be
obtained, which has been regarded as the hypothetical ancestor of all
sponges. A canal system arises when the walls grow thick or form folds, or
give off pouches or tubes. From these channels arise incipient in-current
canals, between the inside or lumen of the folds and that forming the out-
current canal system.
the physiology of digestion in
sponges to permit of a definite
statement on the subject. In
specimens fed upon carmine the
collar-cells have been found loaded
with granules; in others, again, the
flat cells lining the subdermal
cavities have been found gorged with
colour granules. From Bowerbank’s
monograph on the British Spongiadæ
Fig. 342.—An Ascon Sponge.
(1864 and 1874) nothing of
importance can be gained on the
A. Magnified × 20 diameters; B. × 80 diameters; subject; in fact, it relates almost
C. Transverse section; D. Collar-cells, × 700
diameters. The embryo, an extremely minute oval entirely to the structure and
cyst, is furnished with a flagellum for swimming; organisation of sponges in their dried
in the third it assumes an amœboid form (Warne.) or preserved condition, and therefore
is only of value for purposes of
specific identification. One of the simplest of living sponges, the
microscopic structure of which it is possible to trace, Ascetta primordialis,
is found on seaweeds in the Mediterranean. In its simple unbranched
condition it forms a minute white sac about one twenty-fifth of an inch in
height, opening above by a wide round oscule and narrowing below to a
stalk (Fig. 342). The walls are very thin and perforated by pores, through
which the water passes into the interior. The walls of the sac are composed
of two layers, an inner lining of collar-cells, and an outer layer consisting of
a gelatinous matrix containing amœboid bodies and transparent three-rayed
spicules. These serve to support the walls and as a frame-work for the
pores, as in all the sponges. By eliminating the spicular skeleton, and by
supposing the tube to be more globular, the “olynthus form” will be
obtained, which has been regarded as the hypothetical ancestor of all
sponges. A canal system arises when the walls grow thick or form folds, or
give off pouches or tubes. From these channels arise incipient in-current
canals, between the inside or lumen of the folds and that forming the out-
current canal system.
Page 591
There is a common ciliated Sycon found on seaweed round the British
coast; it has the appearance of a white sac about an inch in height, with a
crown of glassy spicules around the orifice. The vertical cavity of the sac is
surrounded by a wall of closely-packed horizontal tubes, opening at their
inner ends into the central cavity, but externally ending blindly. The central
cavity of the sac is surrounded or lined with flat-cells, and the radial tubes
with collar-cells, and the walls of the tubes are perforated. Here the spaces
between and outside the densely-packed tubes are the in-current canals. In
an equally common British sponge, Grantia, which forms small flat white
bags, a rudimentary cortex covers the outer ends of the tubes. In
Grantiopois, the cortex becomes quite thick; as the radial tubes in this
species become more branched and the mesoderm thicker, so the passages
or in-current canals become more complicated. Common silicious, sponges
develop in a different manner from the calcareous ones, namely, from a
hollow conical sac open at the top and with a flat base; the spherical
flagellated chambers at a very early stage forming a mammillated layer in
the walls. Plakina, one of the simplest silicious sponges, encrusts stones
with a fleshy crust, consisting of a sac with a flat base attached to the stone
in sucker-like fashion, and with the rest of the walls forming simple folds.
The spaces between and outside the folds form the in-current, and those in
the lumen of the folds the out-current, channels. Each of the flagellated
chambers in the walls of the folds communicates with the in-current spaces
through several pores, and opens into the out-current spaces by one large
pore, the currents of water passing out by the central oscule. Here we have a
general idea of the formation of all the commoner forms of sponges. In the
more delicate species, as that of Venus’ flowerbasket, the cells are formed
by a trellis work of large spicules of silica. Groups of cells congregate in the
ground substance and secrete a network of cylindrical fibres and spicules,
which, although they remain to a certain extent separate, are always
beautifully adapted for purposes of support. In addition to the support these
afford, the skeleton spicules afford a means of defence against the attacks of
small animals.68
A fairly good idea will be gained of the internal structure of sponges from
the section made of a Geodia Barretti, Fig. 343.
coast; it has the appearance of a white sac about an inch in height, with a
crown of glassy spicules around the orifice. The vertical cavity of the sac is
surrounded by a wall of closely-packed horizontal tubes, opening at their
inner ends into the central cavity, but externally ending blindly. The central
cavity of the sac is surrounded or lined with flat-cells, and the radial tubes
with collar-cells, and the walls of the tubes are perforated. Here the spaces
between and outside the densely-packed tubes are the in-current canals. In
an equally common British sponge, Grantia, which forms small flat white
bags, a rudimentary cortex covers the outer ends of the tubes. In
Grantiopois, the cortex becomes quite thick; as the radial tubes in this
species become more branched and the mesoderm thicker, so the passages
or in-current canals become more complicated. Common silicious, sponges
develop in a different manner from the calcareous ones, namely, from a
hollow conical sac open at the top and with a flat base; the spherical
flagellated chambers at a very early stage forming a mammillated layer in
the walls. Plakina, one of the simplest silicious sponges, encrusts stones
with a fleshy crust, consisting of a sac with a flat base attached to the stone
in sucker-like fashion, and with the rest of the walls forming simple folds.
The spaces between and outside the folds form the in-current, and those in
the lumen of the folds the out-current, channels. Each of the flagellated
chambers in the walls of the folds communicates with the in-current spaces
through several pores, and opens into the out-current spaces by one large
pore, the currents of water passing out by the central oscule. Here we have a
general idea of the formation of all the commoner forms of sponges. In the
more delicate species, as that of Venus’ flowerbasket, the cells are formed
by a trellis work of large spicules of silica. Groups of cells congregate in the
ground substance and secrete a network of cylindrical fibres and spicules,
which, although they remain to a certain extent separate, are always
beautifully adapted for purposes of support. In addition to the support these
afford, the skeleton spicules afford a means of defence against the attacks of
small animals.68
A fairly good idea will be gained of the internal structure of sponges from
the section made of a Geodia Barretti, Fig. 343.
Page 592
Fig. 343.—Geodia Barretti (Bowerbank).
A tangential section of geodia sponge exhibiting the radial disposition of the
fasciculi of the skeleton, and a portion of the mesoderm of the sponge, magnified
50 diameters; a. intermarginal cavities; b. a basal intermarginal cavity; c. ova
imbedded in the dermal crust of the sponge; d. large patentoternate spicula, the
heads of which form areas for the valvular bases of the intermarginal cavities; e.
recurvo-ternate defensive and aggressive spicula within the summits of the
intercellular spaces of the sponge; f. portion of the interstitial membrane of sponge,
crowded with minute stellate spicula; g. portions of the secondary system of
external defensive spicula.
Reproduction.—As regards the modes of reproduction, both male and
female cells are found in the mesoderm. The male cells generally give rise
by division of the nucleus to masses of spermatozoa, each of which
possesses a conical head and a long vibratile filament. The ova appear as
large round cells, and when conglomerated in masses, resemble those of
A tangential section of geodia sponge exhibiting the radial disposition of the
fasciculi of the skeleton, and a portion of the mesoderm of the sponge, magnified
50 diameters; a. intermarginal cavities; b. a basal intermarginal cavity; c. ova
imbedded in the dermal crust of the sponge; d. large patentoternate spicula, the
heads of which form areas for the valvular bases of the intermarginal cavities; e.
recurvo-ternate defensive and aggressive spicula within the summits of the
intercellular spaces of the sponge; f. portion of the interstitial membrane of sponge,
crowded with minute stellate spicula; g. portions of the secondary system of
external defensive spicula.
Reproduction.—As regards the modes of reproduction, both male and
female cells are found in the mesoderm. The male cells generally give rise
by division of the nucleus to masses of spermatozoa, each of which
possesses a conical head and a long vibratile filament. The ova appear as
large round cells, and when conglomerated in masses, resemble those of
Page 593
Micro-gromia, which, after fertilisation, undergo segmentation or division,
first into two cells, and again dividing and sub-dividing, until a cluster or
mass of cells results (as seen in Fig. 343). The outer layer of the egg-shaped
embryo becomes more cylindrical in shape, and is now provided with cilia,
and soon appears as an independent minute oval body. If a bread-crumb
sponge be cut open in the autumn, the embryos will be seen as bright
yellow spots within the body-substance. By keeping specimens in a vessel
of water, the embryos will be seen to escape from the oscules, and swim
freely about with the broad end forwards. After twenty-four hours of
independent existence, the embryo remains stationary, and fixes itself by its
broad end, which becomes flattened out. By a remarkable transformation,
the larger granular cells of the interior burst out and grow over the outer
flagellate layer of cells, and the latter become the collar-cells of the adult
sponge. A minute sponge with one oscule results from the development of
the fertilised ovum. An extensive crust with numerous oscules may be
regarded either as a colony in which each oscule represents an individual, or
simply as one individual in which the growth of the body necessitates the
formation of new channels for the conveyance of food materials. The
embryos of some of the fresh-water sponges (Spongillidæ) living in ponds,
canals, lakes and rivers all over the world, as soon as they become fertilised
undergo segmentation, and form oval ciliated bodies, in appearance
somewhat resembling the gastrula of Monoxenia, one of the simplest kinds
of corals. Fresh-water sponges are green in colour, due to the granular
bodies which crowd the cells near the surface of the sponge; that this colour
is not due to the formation of chlorophyll is seen on keeping them in a
shady place, when they become pale grey or yellowish-brown, and if kept
quite in the dark they entirely lose all colour.
PLATE XVI.
first into two cells, and again dividing and sub-dividing, until a cluster or
mass of cells results (as seen in Fig. 343). The outer layer of the egg-shaped
embryo becomes more cylindrical in shape, and is now provided with cilia,
and soon appears as an independent minute oval body. If a bread-crumb
sponge be cut open in the autumn, the embryos will be seen as bright
yellow spots within the body-substance. By keeping specimens in a vessel
of water, the embryos will be seen to escape from the oscules, and swim
freely about with the broad end forwards. After twenty-four hours of
independent existence, the embryo remains stationary, and fixes itself by its
broad end, which becomes flattened out. By a remarkable transformation,
the larger granular cells of the interior burst out and grow over the outer
flagellate layer of cells, and the latter become the collar-cells of the adult
sponge. A minute sponge with one oscule results from the development of
the fertilised ovum. An extensive crust with numerous oscules may be
regarded either as a colony in which each oscule represents an individual, or
simply as one individual in which the growth of the body necessitates the
formation of new channels for the conveyance of food materials. The
embryos of some of the fresh-water sponges (Spongillidæ) living in ponds,
canals, lakes and rivers all over the world, as soon as they become fertilised
undergo segmentation, and form oval ciliated bodies, in appearance
somewhat resembling the gastrula of Monoxenia, one of the simplest kinds
of corals. Fresh-water sponges are green in colour, due to the granular
bodies which crowd the cells near the surface of the sponge; that this colour
is not due to the formation of chlorophyll is seen on keeping them in a
shady place, when they become pale grey or yellowish-brown, and if kept
quite in the dark they entirely lose all colour.
PLATE XVI.
Page 594
SKELETONS AND SPICULA OF SPONGES.
A few sponges possess no skeleton whatever, excepting the gelatinous
ground substance; in some specimens the skeleton is mainly or entirely
composed of foreign particles of sand or the remains of Foraminifera.
Others are composed of calcium carbonate, and form the class Calcarea, the
spicules of which are white, and opaque in mass; but on placing portions in
hydrochloric acid, the skeleton is dissolved away with effervescence, and
the spicules are left behind transparent and glassy. A great variety is seen in
the different species, as will be gathered from the few typical forms shown
in Plate XVI., and which even in their fossilised state remain unaltered, the
silica which enters so largely into their composition being indestructible,
the calcareous matter alone becoming separated in exposure to the action of
air, or by boiling in hydrochloric acid. The only perceptible difference
A few sponges possess no skeleton whatever, excepting the gelatinous
ground substance; in some specimens the skeleton is mainly or entirely
composed of foreign particles of sand or the remains of Foraminifera.
Others are composed of calcium carbonate, and form the class Calcarea, the
spicules of which are white, and opaque in mass; but on placing portions in
hydrochloric acid, the skeleton is dissolved away with effervescence, and
the spicules are left behind transparent and glassy. A great variety is seen in
the different species, as will be gathered from the few typical forms shown
in Plate XVI., and which even in their fossilised state remain unaltered, the
silica which enters so largely into their composition being indestructible,
the calcareous matter alone becoming separated in exposure to the action of
air, or by boiling in hydrochloric acid. The only perceptible difference
Page 595
noticed is an increase in transparency, and this, on mounting them in
Canada balsam, adds to their beauty when examined by polarised light.
Hyalonema, the “glass-rope” sponge of Japan, consists of a bundle of from
200 to 300 threads of transparent silica, glistening with a satiny lustre like
the most brilliant spun glass; each thread is about eighteen inches long, in
the middle the thickness of a knitting-needle, and gradually tapering
towards either end to a fine point; the whole bundle coiled like a strand of
rope into a lengthened spiral, the threads of the middle and lower portions
remaining compactly coiled by a permanent twist of the individual threads;
the upper portions of the coil frayed out, so that the glassy threads stand
separate from each other. The spicules on the outside of the coil stretch its
entire length, each taking about two and a half turns of the spiral. One of
these long needles is about one-third of a line in diameter in the centre,
gradually tapering towards either end. The spirally-twisted portion of the
needle occupies rather more than the middle half of its entire length. In the
lower portion of the coil, which is embedded in the sponge, the spicule
becomes straight, and tapers down to an extreme tenuity, ultimately
becoming so fine that it is scarcely possible to trace it to its termination.
Within the mesoderm, and in oscule, was noticed a deep brownish-orange
coloured shrunken membrane; this was traced to a parasitic polyp. Since
this was first observed on an early specimen of the Japanese glass-sponge,
the same parasite has always been found growing on and in all these curious
sponges. The surface of the stalk above the portion embedded in the mud is
seen to be covered with a warty crust of parasitic polyps. All the specimens
of Hyalonema in the European museums in 1860 had their stalks overgrown
with Palythoa, while many had their bodies also covered with another
parasite, and which, fortunately for the sponge, did not form a sandy crust.
The polyps, having no skeleton, dry up entirely, and leave behind no trace
except the stain first referred to. Unlike a parasite, however, the polyps do
not feed upon the juices and soft parts of the sponge, nor indeed do they
share its food, but simply settle upon the sponge and feed upon any food
that may chance to come within their reach.
The dredgings of the Challenger brought to the surface many entirely new
forms of glass-sponges and from great depths. One of the most beautiful,
Canada balsam, adds to their beauty when examined by polarised light.
Hyalonema, the “glass-rope” sponge of Japan, consists of a bundle of from
200 to 300 threads of transparent silica, glistening with a satiny lustre like
the most brilliant spun glass; each thread is about eighteen inches long, in
the middle the thickness of a knitting-needle, and gradually tapering
towards either end to a fine point; the whole bundle coiled like a strand of
rope into a lengthened spiral, the threads of the middle and lower portions
remaining compactly coiled by a permanent twist of the individual threads;
the upper portions of the coil frayed out, so that the glassy threads stand
separate from each other. The spicules on the outside of the coil stretch its
entire length, each taking about two and a half turns of the spiral. One of
these long needles is about one-third of a line in diameter in the centre,
gradually tapering towards either end. The spirally-twisted portion of the
needle occupies rather more than the middle half of its entire length. In the
lower portion of the coil, which is embedded in the sponge, the spicule
becomes straight, and tapers down to an extreme tenuity, ultimately
becoming so fine that it is scarcely possible to trace it to its termination.
Within the mesoderm, and in oscule, was noticed a deep brownish-orange
coloured shrunken membrane; this was traced to a parasitic polyp. Since
this was first observed on an early specimen of the Japanese glass-sponge,
the same parasite has always been found growing on and in all these curious
sponges. The surface of the stalk above the portion embedded in the mud is
seen to be covered with a warty crust of parasitic polyps. All the specimens
of Hyalonema in the European museums in 1860 had their stalks overgrown
with Palythoa, while many had their bodies also covered with another
parasite, and which, fortunately for the sponge, did not form a sandy crust.
The polyps, having no skeleton, dry up entirely, and leave behind no trace
except the stain first referred to. Unlike a parasite, however, the polyps do
not feed upon the juices and soft parts of the sponge, nor indeed do they
share its food, but simply settle upon the sponge and feed upon any food
that may chance to come within their reach.
The dredgings of the Challenger brought to the surface many entirely new
forms of glass-sponges and from great depths. One of the most beautiful,
Page 596
known as Carpenter’s glass-sponge (Pheronema), is composed of concentric
laminæ of silica deposited around a fine central axial canal. These form a
gauze-like network throughout, but with no regularity of structure.
Clionæ.—Not the least wonderful circumstance connected with the history
of sponges is the power possessed by certain species of boring into
substances, the hardness of which might be considered as a sufficient
protection against such apparently contemptible foes. Shells (both living
and dead), coral, and even solid rocks are attacked by these humble
destroyers, gradually broken up, and, no doubt, finally reduced to such a
state as to render substances which would otherwise remain dead and
useless in the economy of nature available for the supply of the necessities
of other living creatures.
These boring sponges constitute the genus Cliona of Dr. Grant. They are
branched in form, or consist of lobes united by delicate stems, and after
having buried themselves in shells or other calcareous objects, preserve
their communication with the water by means of perforations in the outer
wall of the shell. The mechanism by which a creature of so low a type of
organisation contrives to produce effects so remarkable is still doubtful,
from the great difficulties which lie in the way of coming to any satisfactory
conclusions upon the habits of an animal that works so completely in the
dark as the Cliona celata. Mr. Hancock, in his valuable memoir upon the
boring sponges, attributes their excavating power to the presence of the
multitude of minute silicious crystalline particles adhering to the surface of
the sponge; these he supposes are set in motion by ciliary action. In
whatever way this action may be produced, however, there can be no doubt
that these sponges are constantly and silently effecting the disintegration of
submarine calcareous bodies—the shelly coverings, it may be, of animals
far higher in organisation, and in many instances they prove themselves
formidable enemies even to living molluscs, by boring completely through
the shell. In this case the animal whose domicile it so unceremoniously
invades has no alternative but to raise a wall of new shelly matter between
himself and his unwelcome guest, and in this manner generally succeeds in
barring him out.
laminæ of silica deposited around a fine central axial canal. These form a
gauze-like network throughout, but with no regularity of structure.
Clionæ.—Not the least wonderful circumstance connected with the history
of sponges is the power possessed by certain species of boring into
substances, the hardness of which might be considered as a sufficient
protection against such apparently contemptible foes. Shells (both living
and dead), coral, and even solid rocks are attacked by these humble
destroyers, gradually broken up, and, no doubt, finally reduced to such a
state as to render substances which would otherwise remain dead and
useless in the economy of nature available for the supply of the necessities
of other living creatures.
These boring sponges constitute the genus Cliona of Dr. Grant. They are
branched in form, or consist of lobes united by delicate stems, and after
having buried themselves in shells or other calcareous objects, preserve
their communication with the water by means of perforations in the outer
wall of the shell. The mechanism by which a creature of so low a type of
organisation contrives to produce effects so remarkable is still doubtful,
from the great difficulties which lie in the way of coming to any satisfactory
conclusions upon the habits of an animal that works so completely in the
dark as the Cliona celata. Mr. Hancock, in his valuable memoir upon the
boring sponges, attributes their excavating power to the presence of the
multitude of minute silicious crystalline particles adhering to the surface of
the sponge; these he supposes are set in motion by ciliary action. In
whatever way this action may be produced, however, there can be no doubt
that these sponges are constantly and silently effecting the disintegration of
submarine calcareous bodies—the shelly coverings, it may be, of animals
far higher in organisation, and in many instances they prove themselves
formidable enemies even to living molluscs, by boring completely through
the shell. In this case the animal whose domicile it so unceremoniously
invades has no alternative but to raise a wall of new shelly matter between
himself and his unwelcome guest, and in this manner generally succeeds in
barring him out.
Page 597
From a close examination of the structural and developmental characters of
the Spongideæ, it must be conceded that they belong rather to the flagellata
Protozoa than to any other order. This was the view held by the late
Professor Clark, and Mr. Saville Kent quite concurs in it.69 Summing up the
entire evidence adduced, scarcely a shadow of doubt is admissible
concerning the intimate relationship that subsists between the Choano-
flagellata and other flagellate Protozoa and that of sponges. The primary
and essential element of the apparently complex sponge stock is the
assemblage of collared flagellate zooids that inhabit its interstitial cavities
under various plans of distribution. Individually these collared zooids
correspond structurally and functionally in every detail with the collared
units of such genera as Codosiga, Salpingœca, and Proto-spongia. The
collar in either case presents the same structure and functions, exhibits the
same circulatory currents or cyclosis, and acts in the same way for the
capture of food. The body contains an identical centrally located spheroidal
nucleus or endoplast, and a corresponding series of rhythmically pulsating
contractile vesicles. The developmental reproductive phenomena are also
strictly parallel. Both originate as simple Amœba or simple flagellate
Monads, exhibiting no trace in their earliest stage of the subsequently
acquired characteristic collar. Both again after a time withdraw their collar
and flagellum, and assume the amœboid state; then, coalescing, enter upon
a quiescent or encysted condition, and break up into a number of sporular
bodies, and thus provide for the further existence and distribution of the
species. The whole process again is much akin to that which obtains in the
protophytic type, Volvox globator, which liberates from its interior free
swimming gemmules that take the form of spherical aggregation of
biflagellate daughter-cells. In their isolated state, on the other hand, the
swarm gemmules of the sponge stock are directly comparable with the free
swimming subspheroidal colony stock of the flagellate infusoria Synura,
Syncrypta, and Uroglena, or with the attached subspheroidal clusters of
Codosiga and Anthophysa.
Echinodermata, Hydrozoa, Polyzoa, Helminthoida.
the Spongideæ, it must be conceded that they belong rather to the flagellata
Protozoa than to any other order. This was the view held by the late
Professor Clark, and Mr. Saville Kent quite concurs in it.69 Summing up the
entire evidence adduced, scarcely a shadow of doubt is admissible
concerning the intimate relationship that subsists between the Choano-
flagellata and other flagellate Protozoa and that of sponges. The primary
and essential element of the apparently complex sponge stock is the
assemblage of collared flagellate zooids that inhabit its interstitial cavities
under various plans of distribution. Individually these collared zooids
correspond structurally and functionally in every detail with the collared
units of such genera as Codosiga, Salpingœca, and Proto-spongia. The
collar in either case presents the same structure and functions, exhibits the
same circulatory currents or cyclosis, and acts in the same way for the
capture of food. The body contains an identical centrally located spheroidal
nucleus or endoplast, and a corresponding series of rhythmically pulsating
contractile vesicles. The developmental reproductive phenomena are also
strictly parallel. Both originate as simple Amœba or simple flagellate
Monads, exhibiting no trace in their earliest stage of the subsequently
acquired characteristic collar. Both again after a time withdraw their collar
and flagellum, and assume the amœboid state; then, coalescing, enter upon
a quiescent or encysted condition, and break up into a number of sporular
bodies, and thus provide for the further existence and distribution of the
species. The whole process again is much akin to that which obtains in the
protophytic type, Volvox globator, which liberates from its interior free
swimming gemmules that take the form of spherical aggregation of
biflagellate daughter-cells. In their isolated state, on the other hand, the
swarm gemmules of the sponge stock are directly comparable with the free
swimming subspheroidal colony stock of the flagellate infusoria Synura,
Syncrypta, and Uroglena, or with the attached subspheroidal clusters of
Codosiga and Anthophysa.
Echinodermata, Hydrozoa, Polyzoa, Helminthoida.
Page 598
Tuffen West, del. Edmund Evans.
Plate IV.
Plate IV.
Page 599
CHAPTER III.
Zoophytes, Cœlenterata, Medusæ, Corals, Hydrozoa.
A study of the earliest growth of the Cœlenterata has
shown that their internal cavities are nothing more
than regular radiate out-growths of the internal
structures. The result of this development is a
condition which does not occur again in the whole
of the animal kingdom. There is a system of cavities
all in open communication one with another, no
closed blood vascular system, and no specialised
respiratory apparatus. Again, all the animals that
constitute this large group are radiate in structure,
that is, when viewed from above they are typically
star-shaped, and if cut across, every horizontal
section shows a symmetrical arrangement of the
several parts around a centre. There are other radiate
animals, as the Echinoderms, but while in these five
is the fundamental number of rays, in the
Cœlenterata the rays are a multiple of four, six and
upwards. The skeleton or framework of each differs,
and when the Cœlenterata form calcareous
structures, these are quite different from the tests of
the sea-urchins; and in all cases the anterior portion
of the body is crowned with one or more circles of
tentacles, which remain perfectly flexible and Fig. 344.—Gorgonia Nobilis.
flower-like. The most highly-developed of the free
forms are the sea-anemones and the jelly-fish. These have no hard or
calcareous skeleton whatever, but withal they are, in the opinion of
naturalists and microscopists, the most beautiful objects among Zoophytes.
Zoophytes, Cœlenterata, Medusæ, Corals, Hydrozoa.
A study of the earliest growth of the Cœlenterata has
shown that their internal cavities are nothing more
than regular radiate out-growths of the internal
structures. The result of this development is a
condition which does not occur again in the whole
of the animal kingdom. There is a system of cavities
all in open communication one with another, no
closed blood vascular system, and no specialised
respiratory apparatus. Again, all the animals that
constitute this large group are radiate in structure,
that is, when viewed from above they are typically
star-shaped, and if cut across, every horizontal
section shows a symmetrical arrangement of the
several parts around a centre. There are other radiate
animals, as the Echinoderms, but while in these five
is the fundamental number of rays, in the
Cœlenterata the rays are a multiple of four, six and
upwards. The skeleton or framework of each differs,
and when the Cœlenterata form calcareous
structures, these are quite different from the tests of
the sea-urchins; and in all cases the anterior portion
of the body is crowned with one or more circles of
tentacles, which remain perfectly flexible and Fig. 344.—Gorgonia Nobilis.
flower-like. The most highly-developed of the free
forms are the sea-anemones and the jelly-fish. These have no hard or
calcareous skeleton whatever, but withal they are, in the opinion of
naturalists and microscopists, the most beautiful objects among Zoophytes.
Page 600
In spite of their variety of forms, the Cœlenterata seem to be as incapable of
higher development as do the Echinoderms, and they have failed to make
headway in fresh water, but it is not improbable that some of the simplest
forms of the whole group may have given rise to higher animal forms,
while the sea anemones, corals, &c., being those descendants of the
primitive simple form, have retained the original type of organization
almost unchanged.
Fig. 345.—Hydra viridis, adhering to a stalk of Anacharis alsinastrum.
The type of the group is the Hydra, a fresh-water polyp, commonly found
attached to the leaves and stems of many aquatic plants, or floating pieces
of stick. Two species are well known to microscopists, the H. viridis, or
green polyp, and the H. vulgaris, somewhat darker in colour, probably
dependent upon the nature of its food. The third, less common species, the
H. fasca, is distinguished from both by the length of its tentacles, which,
when fully extended, greatly exceed those of either of the before-
higher development as do the Echinoderms, and they have failed to make
headway in fresh water, but it is not improbable that some of the simplest
forms of the whole group may have given rise to higher animal forms,
while the sea anemones, corals, &c., being those descendants of the
primitive simple form, have retained the original type of organization
almost unchanged.
Fig. 345.—Hydra viridis, adhering to a stalk of Anacharis alsinastrum.
The type of the group is the Hydra, a fresh-water polyp, commonly found
attached to the leaves and stems of many aquatic plants, or floating pieces
of stick. Two species are well known to microscopists, the H. viridis, or
green polyp, and the H. vulgaris, somewhat darker in colour, probably
dependent upon the nature of its food. The third, less common species, the
H. fasca, is distinguished from both by the length of its tentacles, which,
when fully extended, greatly exceed those of either of the before-
Page 601
mentioned. The fresh-water group measures from one-eighth to the one-
third of an inch in length, and form simple stocks of one, two or more
branches. They almost exactly resemble in form the polyps of the
Hydractinia, which are provided with a circle of tentacles. When placed in a
vessel of water and left undisturbed they often attach themselves to the side,
where they may be examined with a moderate power at leisure. They are
then seen to spread out their tentacles like fine threads, and seize upon any
small creature that may come in their way, and by the same means convey it
to a mouth capable of great extension. All Hydra possess stinging-cells, by
means of which they paralyse their prey. Many Hydra attain to a large size,
and shoot out long poisonous filaments; they also possess smaller kinds of
smooth cells, which appear to be employed for an entirely different
purpose, but for what is not positively known. Hydra usually multiply by
means of buds, an out-growth from the body, and these remain attached to
the mother stalk for some time, often long enough to give rise to one or two
smaller buds. Single eggs are also developed in the ectoderm beneath
capsules, or wart-like prominences. The adult animal can be cut to pieces,
and from each piece a new individual will be developed. This method of
reproduction was first tried by the naturalist Trembley in 1739, whose
experiments in this direction excited the greatest interest among the
naturalists of the middle of the last century. Hydra fusca in various stages of
development is given in outline in Fig. 346.
third of an inch in length, and form simple stocks of one, two or more
branches. They almost exactly resemble in form the polyps of the
Hydractinia, which are provided with a circle of tentacles. When placed in a
vessel of water and left undisturbed they often attach themselves to the side,
where they may be examined with a moderate power at leisure. They are
then seen to spread out their tentacles like fine threads, and seize upon any
small creature that may come in their way, and by the same means convey it
to a mouth capable of great extension. All Hydra possess stinging-cells, by
means of which they paralyse their prey. Many Hydra attain to a large size,
and shoot out long poisonous filaments; they also possess smaller kinds of
smooth cells, which appear to be employed for an entirely different
purpose, but for what is not positively known. Hydra usually multiply by
means of buds, an out-growth from the body, and these remain attached to
the mother stalk for some time, often long enough to give rise to one or two
smaller buds. Single eggs are also developed in the ectoderm beneath
capsules, or wart-like prominences. The adult animal can be cut to pieces,
and from each piece a new individual will be developed. This method of
reproduction was first tried by the naturalist Trembley in 1739, whose
experiments in this direction excited the greatest interest among the
naturalists of the middle of the last century. Hydra fusca in various stages of
development is given in outline in Fig. 346.
Page 602
Fig. 346.
1, 2, 3. Hydra in various stages of development; 4. Group of Stentor polymorphus,
many-shaped Stentor; 5. Englena; 6. Monads.
In the polyps belonging to this family the body-structure for the most part
consists of a homogeneous aggregation of vesicular granules, held together
by an intercellular sarcode, and capable of great extension and contraction,
so that these animals can assume a variety of forms and extend their body
and tentacles until the latter become almost invisible. It was the
resemblance in this respect to the fabled Hydra that originated the name. Its
organ of prehension is termed the hasta; this consists of a sac or opening at
the terminal end of the tentacle, within which is seen a saucer-shaped
vesicle, supporting a minute ovate body, which carries a sharp calcareous
piece termed a sagitta or arrow. Although the fresh-water Hydra may be
1, 2, 3. Hydra in various stages of development; 4. Group of Stentor polymorphus,
many-shaped Stentor; 5. Englena; 6. Monads.
In the polyps belonging to this family the body-structure for the most part
consists of a homogeneous aggregation of vesicular granules, held together
by an intercellular sarcode, and capable of great extension and contraction,
so that these animals can assume a variety of forms and extend their body
and tentacles until the latter become almost invisible. It was the
resemblance in this respect to the fabled Hydra that originated the name. Its
organ of prehension is termed the hasta; this consists of a sac or opening at
the terminal end of the tentacle, within which is seen a saucer-shaped
vesicle, supporting a minute ovate body, which carries a sharp calcareous
piece termed a sagitta or arrow. Although the fresh-water Hydra may be
Page 603
regarded as typical of this group of animals, marine fauna furnish a far
more extensive group in the corals, jelly-fish, and sea-anemones.
A smaller group, the Ctenophora, although members of this sub-kingdom,
have not yet found their true position; nevertheless they are interesting
glassy, transparent creatures, either shaped like apples, melons, or Phrygian
caps, or else forming bands of some considerable length; all are
wonderfully transparent, with the single exception of the Beroë. These
inhabit the open sea, and are only seen inshore when driven in by currents
or strong winds. Their position in the water is usually more or less vertical,
the mouth being turned downwards. The portion from which this group
derives its name is the ribs, which are symmetrically arranged, and consist
of rows of short transverse combs, each forming rows of cilia, which, as
they wave to and fro, constitute a swimming or rowing plate, their activity
in the water depending upon the will of the animal. They are also provided
with an oral umbrella, and capturing filaments or tentacles with hair-like
branches. These tentacles, attached to the sides of the animal, are capable of
erection or withdrawal into pockets. Great variety is seen in these accessory
organs of locomotion; for instance, the Cydippidæ (Plate XVII.) have only
arms, but these are remarkable for their length, and serve for the purpose of
capturing food as well as for steering. The most interesting, if not the most
beautiful of the Ctenophora, are the Beroidæ; it is this family that bear a
resemblance to the Phrygian cap (Plate XVII., e). The mouth is wide, but it
appears to have no capturing tentacles, and yet their habits are carnivorous;
they will even devour their own relations. Many of the genus are
phosphorescent, and in place of stinging-cells have small spherical knobs
beset with sticky globules, in which their food becomes entangled, and
these are apparently in constant use.
PLATE XVII.
more extensive group in the corals, jelly-fish, and sea-anemones.
A smaller group, the Ctenophora, although members of this sub-kingdom,
have not yet found their true position; nevertheless they are interesting
glassy, transparent creatures, either shaped like apples, melons, or Phrygian
caps, or else forming bands of some considerable length; all are
wonderfully transparent, with the single exception of the Beroë. These
inhabit the open sea, and are only seen inshore when driven in by currents
or strong winds. Their position in the water is usually more or less vertical,
the mouth being turned downwards. The portion from which this group
derives its name is the ribs, which are symmetrically arranged, and consist
of rows of short transverse combs, each forming rows of cilia, which, as
they wave to and fro, constitute a swimming or rowing plate, their activity
in the water depending upon the will of the animal. They are also provided
with an oral umbrella, and capturing filaments or tentacles with hair-like
branches. These tentacles, attached to the sides of the animal, are capable of
erection or withdrawal into pockets. Great variety is seen in these accessory
organs of locomotion; for instance, the Cydippidæ (Plate XVII.) have only
arms, but these are remarkable for their length, and serve for the purpose of
capturing food as well as for steering. The most interesting, if not the most
beautiful of the Ctenophora, are the Beroidæ; it is this family that bear a
resemblance to the Phrygian cap (Plate XVII., e). The mouth is wide, but it
appears to have no capturing tentacles, and yet their habits are carnivorous;
they will even devour their own relations. Many of the genus are
phosphorescent, and in place of stinging-cells have small spherical knobs
beset with sticky globules, in which their food becomes entangled, and
these are apparently in constant use.
PLATE XVII.
Page 604
ZOOPHYTES, ASTEROIDS, NUDIBRANCHIS, ACALEPS, ECHINOIDS,
CTENOPHORA, TUNICATA, AND CRUSTACEANS.
The Stinging Series, Cnidaria, comprise sea-anemones, corals, jelly-fish
among marine animals, and Hydra among the fresh-water Cœlenterata; and
derive their name from a remarkably curious feature, the so-called stinging
capsules. These are not only offensive, but also defensive weapons with all
the animals belonging to this group; the possession of which has converted
the bell-like jelly-fish into a simple Cnidarian. The principal change is in
the gelatinous layer between the outer wall and the inner digesting layer of
the ectoderm. But without entering further into their structure and relations,
the stinging-cells and batteries claim especial attention. These cells vary
considerably in size without their characteristics being essentially changed.
The protoplasm of the cell is modified into a tolerably firm substance,
enclosing an oval or cylindrical vesicle. Closely associated with this is a
CTENOPHORA, TUNICATA, AND CRUSTACEANS.
The Stinging Series, Cnidaria, comprise sea-anemones, corals, jelly-fish
among marine animals, and Hydra among the fresh-water Cœlenterata; and
derive their name from a remarkably curious feature, the so-called stinging
capsules. These are not only offensive, but also defensive weapons with all
the animals belonging to this group; the possession of which has converted
the bell-like jelly-fish into a simple Cnidarian. The principal change is in
the gelatinous layer between the outer wall and the inner digesting layer of
the ectoderm. But without entering further into their structure and relations,
the stinging-cells and batteries claim especial attention. These cells vary
considerably in size without their characteristics being essentially changed.
The protoplasm of the cell is modified into a tolerably firm substance,
enclosing an oval or cylindrical vesicle. Closely associated with this is a
Page 605
pointed process, standing up far above the level of the outer covering,
known as the cnidocil. Within the vesicle is found, either spirally rolled up
or in an irregular tangle, a long filament or hollow tube, a prolongation of
the vesicle, but turned outside in. This tube is more than twenty times as
long as the cell, is pointed at the tip, and beset with two rows of fine
spirally-arranged barbed hooks. When the cnidocil is touched or irritated,
this filament is violently shot out, being then turned inside-out, like the
fingers of a glove. So long as the thread remains rolled up within the vesicle
the barbed hooks remain in their tube, but when shot out, they change to the
outside. The rolled-up filament appears to be filled with some poisonous
material, which is ejected when the tube is shot out, and where the point
strikes a wound is inflicted, so that unless the prey is stronger than the
attacker it cannot escape. The greater the struggle, the larger the number of
capsules discharged in order to kill.
known as the cnidocil. Within the vesicle is found, either spirally rolled up
or in an irregular tangle, a long filament or hollow tube, a prolongation of
the vesicle, but turned outside in. This tube is more than twenty times as
long as the cell, is pointed at the tip, and beset with two rows of fine
spirally-arranged barbed hooks. When the cnidocil is touched or irritated,
this filament is violently shot out, being then turned inside-out, like the
fingers of a glove. So long as the thread remains rolled up within the vesicle
the barbed hooks remain in their tube, but when shot out, they change to the
outside. The rolled-up filament appears to be filled with some poisonous
material, which is ejected when the tube is shot out, and where the point
strikes a wound is inflicted, so that unless the prey is stronger than the
attacker it cannot escape. The greater the struggle, the larger the number of
capsules discharged in order to kill.
Page 606
Fig. 347.—The Stinging Capsules of Cnidaria.
1 and 2. Retracted filaments; 3. Partly protruded; 4. Fully protruded. Magnified ×
600. (Warne.)
Polypomedusæ.—Among the higher development of the stinging group is
the jelly-fish. The Siphonophora, as represented by the Portuguese man-of-
war, are in their turn the highest development of swimming-bells, and
exhibit many modifications and combinations of individuals. The tentacles
of the Physalia, the best known, are stiff with batteries of stinging-capsules,
the sting of which is more like the shock of the electric current. The
Challenger soundings brought to light some remarkably interesting forms,
and these have furnished much work for the microscope, as all their larval
forms are extremely curious. Among the Hydromedusæ there are many
different life histories. Take the jelly-fish, the eggs of which have given up
forming stocks, and are hatched out at once as Medusæ. There are others,
the eggs of which form stocks; others, again, in which the sexual
individuals do not swim away as jelly-fish. The last were at one time
described under a new name, because of one or two curious forms being
taken creeping on the ground. This creeping Medusa (Clavatella prolifera)
has six arms, the tips of which are provided with true suckers, and on these
it walks as on stilts, while from each arm a short stalk arises, the swollen
end of which is beset with stinging capsules. It has an extensile mouth-tube,
and feeds upon small crustaceans found on seaweeds.
Among the forms that swim away as jelly-fish a very curious example is
presented in Corymorpha mutans. These swim about for a time, and then
firmly attach themselves by numerous thread-like appendages, forced into
the sand, and where the young prepare for their next metamorphosis. As an
example of the stocks of those representatives which do not swim away as
jelly-fish, take the beautifully-feathered, plant-like creatures found erect
along the seashore, the Sertularia (Fig. 358, No. 12) and Plumularia.
Plumularia primata, Fig. 348. Other members of these groups will be found
in Plate IV., Nos. 95-99.
1 and 2. Retracted filaments; 3. Partly protruded; 4. Fully protruded. Magnified ×
600. (Warne.)
Polypomedusæ.—Among the higher development of the stinging group is
the jelly-fish. The Siphonophora, as represented by the Portuguese man-of-
war, are in their turn the highest development of swimming-bells, and
exhibit many modifications and combinations of individuals. The tentacles
of the Physalia, the best known, are stiff with batteries of stinging-capsules,
the sting of which is more like the shock of the electric current. The
Challenger soundings brought to light some remarkably interesting forms,
and these have furnished much work for the microscope, as all their larval
forms are extremely curious. Among the Hydromedusæ there are many
different life histories. Take the jelly-fish, the eggs of which have given up
forming stocks, and are hatched out at once as Medusæ. There are others,
the eggs of which form stocks; others, again, in which the sexual
individuals do not swim away as jelly-fish. The last were at one time
described under a new name, because of one or two curious forms being
taken creeping on the ground. This creeping Medusa (Clavatella prolifera)
has six arms, the tips of which are provided with true suckers, and on these
it walks as on stilts, while from each arm a short stalk arises, the swollen
end of which is beset with stinging capsules. It has an extensile mouth-tube,
and feeds upon small crustaceans found on seaweeds.
Among the forms that swim away as jelly-fish a very curious example is
presented in Corymorpha mutans. These swim about for a time, and then
firmly attach themselves by numerous thread-like appendages, forced into
the sand, and where the young prepare for their next metamorphosis. As an
example of the stocks of those representatives which do not swim away as
jelly-fish, take the beautifully-feathered, plant-like creatures found erect
along the seashore, the Sertularia (Fig. 358, No. 12) and Plumularia.
Plumularia primata, Fig. 348. Other members of these groups will be found
in Plate IV., Nos. 95-99.
Page 607
Fig. 348.—Plumularia primata. Doris tuberculata
seen clinging to a fucus.
seen clinging to a fucus.
Page 608
Fig. 349.—Group of female stock of Hydractinia echinata.
a, a. Nutritive individuals; b, b. Female individuals and groups of eggs. Highly
magnified.—(Warne.)
In addition to the nutritive individuals, there are the egg-bearing; these do
not become free-swimming individuals. One small family is neither
branched nor feathered—the Hydractinia echinata, found in the North Sea
and on the Norwegian coasts, where it attaches itself to the shells of
gastropods, selecting those inhabited by hermit crabs. The part of the stock
common to all the individuals is the skin-like portion which adheres to the
surface of the shell. In some spiny processes are produced, and the nutritive
canals running down the stems of the polyps are continued into the
membrane belonging to the stock, as seen in Fig. 349.
a, a. Nutritive individuals; b, b. Female individuals and groups of eggs. Highly
magnified.—(Warne.)
In addition to the nutritive individuals, there are the egg-bearing; these do
not become free-swimming individuals. One small family is neither
branched nor feathered—the Hydractinia echinata, found in the North Sea
and on the Norwegian coasts, where it attaches itself to the shells of
gastropods, selecting those inhabited by hermit crabs. The part of the stock
common to all the individuals is the skin-like portion which adheres to the
surface of the shell. In some spiny processes are produced, and the nutritive
canals running down the stems of the polyps are continued into the
membrane belonging to the stock, as seen in Fig. 349.
Page 609
The nutritive individuals are distinguished by long tentacles, mouths, and
digestive canals. The females have no mouths, and are supplied with food
through the system of canals running to them from the nutritive males.
These reproductive members are furnished with stinging threads instead of
tentacles for the protection of their ova. The ciliated larvæ, in a very short
time, swim off to found new colonies.
The free-swimming jelly-fish (Fig. 350, and Plate
XVII., c and d) belong to the order
Scyphomedusæ. These are characterised by their
delicate colouring, and from the arrangement of
their nervous system, which can only be made out
by staining. Some new and curious forms were
dredged from a depth of more than 6,000 feet off
the coast of New Zealand, varying in size from an
inch to twenty inches; many having from four to
eight or ten eyes arranged along the margin.
Anthozoa.—From the free-swimming we turn to a
group of permanently fixed polyp forms, the sea-
anemones and corals. The development of
Monoxenia commences with the egg, repeatedly
dividing into many parts (Fig. 351, C, D, and E),
by a process common to the animal kingdom, Fig. 350.—Medusæ, Jelly-fish.
termed egg-segmentation, in this particular
instance proceeding from an apparently hollow sphere, A, enclosing a single
layer of cells, G. Each cell sends out a long cilia, or whip-like process, F, by
means of which the larva turns about and swims in the body fluid of the
parent polyp. One half of the sphere now becomes enfolded into the other
half, H, and forms what is termed a gastrula, I, K. The gastrula stage of
Monoxenia is of the simplest kind, the larva forming a sac, with walls
consisting of two layers, an outer, or ectoderm, and an inner, or endoderm.
The transition from the flat dish shape, H, to the sac with a narrow mouth is
at once clear, and the knowledge that all the Cœlenterates proceed from
similar larvæ, and that all the complications of their various systems are
developed from a simple gastrula, throws much light on their anatomy.
During these transitions the endoderm, whose cells multiply, continues as
digestive canals. The females have no mouths, and are supplied with food
through the system of canals running to them from the nutritive males.
These reproductive members are furnished with stinging threads instead of
tentacles for the protection of their ova. The ciliated larvæ, in a very short
time, swim off to found new colonies.
The free-swimming jelly-fish (Fig. 350, and Plate
XVII., c and d) belong to the order
Scyphomedusæ. These are characterised by their
delicate colouring, and from the arrangement of
their nervous system, which can only be made out
by staining. Some new and curious forms were
dredged from a depth of more than 6,000 feet off
the coast of New Zealand, varying in size from an
inch to twenty inches; many having from four to
eight or ten eyes arranged along the margin.
Anthozoa.—From the free-swimming we turn to a
group of permanently fixed polyp forms, the sea-
anemones and corals. The development of
Monoxenia commences with the egg, repeatedly
dividing into many parts (Fig. 351, C, D, and E),
by a process common to the animal kingdom, Fig. 350.—Medusæ, Jelly-fish.
termed egg-segmentation, in this particular
instance proceeding from an apparently hollow sphere, A, enclosing a single
layer of cells, G. Each cell sends out a long cilia, or whip-like process, F, by
means of which the larva turns about and swims in the body fluid of the
parent polyp. One half of the sphere now becomes enfolded into the other
half, H, and forms what is termed a gastrula, I, K. The gastrula stage of
Monoxenia is of the simplest kind, the larva forming a sac, with walls
consisting of two layers, an outer, or ectoderm, and an inner, or endoderm.
The transition from the flat dish shape, H, to the sac with a narrow mouth is
at once clear, and the knowledge that all the Cœlenterates proceed from
similar larvæ, and that all the complications of their various systems are
developed from a simple gastrula, throws much light on their anatomy.
During these transitions the endoderm, whose cells multiply, continues as
Page 610
an uninterrupted lining to the stomach and its appendages, while the
ectoderm yields the cuticular elements.
Fig. 351.—Stages in development of Monoxenia Darwinii, × 600.—(Warne.)
A third intermediate gelatinous layer, the mesoglæa, arises between the two
layers in which muscles and connective interstitial tissue appear. In the
mesoglæa of one species of coral calcification takes place; this internal
calcification has but a small share in the work of the great rock-making
corals, their most important calcification being external. In Monoxenia,
although the transition from the gastrula larva to the adult animal has not
been seen, there can be no doubt as to how this is carried out, the
transformations having been watched throughout in other species. The larva
attaches itself with the end opposite the mouth, the cilia disappear, and after
the mouth-tube has been formed by the folding in of the anterior end along
ectoderm yields the cuticular elements.
Fig. 351.—Stages in development of Monoxenia Darwinii, × 600.—(Warne.)
A third intermediate gelatinous layer, the mesoglæa, arises between the two
layers in which muscles and connective interstitial tissue appear. In the
mesoglæa of one species of coral calcification takes place; this internal
calcification has but a small share in the work of the great rock-making
corals, their most important calcification being external. In Monoxenia,
although the transition from the gastrula larva to the adult animal has not
been seen, there can be no doubt as to how this is carried out, the
transformations having been watched throughout in other species. The larva
attaches itself with the end opposite the mouth, the cilia disappear, and after
the mouth-tube has been formed by the folding in of the anterior end along
Page 611
the longitudinal axis of the body, and has thus become marked off from the
stomach, eight hollow tentacles rise round the mouth as outgrowths of the
body cavity, or as direct continuations of the stomach.
Like all other corals, Monoxenia periodically multiply by means of eggs,
which are formed either in the walls of the radiating partitions or septa, or
along the free edges. These are ejected through the oral opening. As a rule,
the polyps are either male or female; but in stock-forming species
individuals of the two sexes are often mixed. Monoxenia may be taken as
the simplest type of the regularly radiate polyps; in all the different organs
being repeated in regular rings round a central axis; the mouth also is
circular. From this interesting account, drawn by Haeckel, of a simple
polyp, it will be at once seen what kind of radiate animal it is that builds up
the coral reefs. “No garden on earth can match the gardens of the sea that
circle the northern part of Australia. As the tide ebbs in azure sunset, coral-
reefs peer out symmetrically arranged in beds and intersected by emerald
pathways coursing through corals of all hues and tints fathoms deep in the
channels.”
In a growing polyp-stock the individuals usually remain in organic
connection; that is to say, each first provides for itself and then shares its
superfluity with others, sometimes by means of a continuous reticulated
system of canals perforating the calcareous substance which often separates
the members of one stock from another. The whole colony may thus be
physiologically one creature with many mouths. There are others that
remain single, as the inverted pyramidal-looking bodies, Fungidæ,
commonly called “Sea-mushrooms,” found in great variety. The colour of
the polypidom is white, of a flattened round shape, made up of thin plates
or scales, imbedded in a translucent jelly-like substance, and within is
concealed a polyp; the footstalk, by means of which the animal is attached
to the rock, is of a calcareous nature (Fig. 352, No. 1).
stomach, eight hollow tentacles rise round the mouth as outgrowths of the
body cavity, or as direct continuations of the stomach.
Like all other corals, Monoxenia periodically multiply by means of eggs,
which are formed either in the walls of the radiating partitions or septa, or
along the free edges. These are ejected through the oral opening. As a rule,
the polyps are either male or female; but in stock-forming species
individuals of the two sexes are often mixed. Monoxenia may be taken as
the simplest type of the regularly radiate polyps; in all the different organs
being repeated in regular rings round a central axis; the mouth also is
circular. From this interesting account, drawn by Haeckel, of a simple
polyp, it will be at once seen what kind of radiate animal it is that builds up
the coral reefs. “No garden on earth can match the gardens of the sea that
circle the northern part of Australia. As the tide ebbs in azure sunset, coral-
reefs peer out symmetrically arranged in beds and intersected by emerald
pathways coursing through corals of all hues and tints fathoms deep in the
channels.”
In a growing polyp-stock the individuals usually remain in organic
connection; that is to say, each first provides for itself and then shares its
superfluity with others, sometimes by means of a continuous reticulated
system of canals perforating the calcareous substance which often separates
the members of one stock from another. The whole colony may thus be
physiologically one creature with many mouths. There are others that
remain single, as the inverted pyramidal-looking bodies, Fungidæ,
commonly called “Sea-mushrooms,” found in great variety. The colour of
the polypidom is white, of a flattened round shape, made up of thin plates
or scales, imbedded in a translucent jelly-like substance, and within is
concealed a polyp; the footstalk, by means of which the animal is attached
to the rock, is of a calcareous nature (Fig. 352, No. 1).
Page 612
Fig. 352.—Sea-Anemones.
1. Actinia rubra, tentacles displayed and retracted; 2. Heticictis bellis; 3. H. bellis,
seen from above.
Hexactinia (six-rayed polyps) are not limited to six rays, as the name given
them may seem to imply; they are, in fact, very numerous in some of the
largest and most gorgeous of the sea-anemones. All are distinguished by
their solitary manner of life, their size, and their vivid and variedly beautiful
colouring. The endoderm is firm, and when the animal withdraws its
tentacles and shuts its body substance in, there is some difficulty in
penetrating to the interior. It does not, however, secrete a calcareous
skeleton inside or out, as do the true coral polyps. Among the Hexactinia
the sea-anemone (Fig. 352) takes the first place.
These beautifully coloured creatures are, for the most part, found attached
to the spot selected by the larvæ; a few species bore into the sand with the
posterior part of the body, or build a sheath, which they inhabit. They are
voracious feeders, and devour large pieces of flesh, and even mussel and
oysters, sucking them in by means of their long grasping tentacles. Well-fed
anemones change their skin frequently, during which process they remain
closely retracted; the shed skin forms a loose girdle around the base. Actinia
bellis not infrequently attach themselves to the shells of crabs and whelks,
and are thus carried to pastures new.
1. Actinia rubra, tentacles displayed and retracted; 2. Heticictis bellis; 3. H. bellis,
seen from above.
Hexactinia (six-rayed polyps) are not limited to six rays, as the name given
them may seem to imply; they are, in fact, very numerous in some of the
largest and most gorgeous of the sea-anemones. All are distinguished by
their solitary manner of life, their size, and their vivid and variedly beautiful
colouring. The endoderm is firm, and when the animal withdraws its
tentacles and shuts its body substance in, there is some difficulty in
penetrating to the interior. It does not, however, secrete a calcareous
skeleton inside or out, as do the true coral polyps. Among the Hexactinia
the sea-anemone (Fig. 352) takes the first place.
These beautifully coloured creatures are, for the most part, found attached
to the spot selected by the larvæ; a few species bore into the sand with the
posterior part of the body, or build a sheath, which they inhabit. They are
voracious feeders, and devour large pieces of flesh, and even mussel and
oysters, sucking them in by means of their long grasping tentacles. Well-fed
anemones change their skin frequently, during which process they remain
closely retracted; the shed skin forms a loose girdle around the base. Actinia
bellis not infrequently attach themselves to the shells of crabs and whelks,
and are thus carried to pastures new.
Page 613
Fig. 353.—Larvæ of Sea-Anemones, Actinia effœta, highly magnified.
On account of the ease with which anemones are kept in captivity, their
mode of reproduction can be closely observed. With but few exceptions
they develop from eggs, and in the course of a few weeks are hatched into
ciliated infusorial larvæ, presenting most curious and exquisite
representations of jugs and jars, with cover lids (as seen in Fig. 353, Actinia
effœta). These evince the handiwork of a master hand in the ceramic art.
They are, however, of so translucent a nature as to permit of the internal
structure being seen to consist of nerves and vessels, and which are
rendered more apparent by staining. These settle down in a week or ten
days, and then shed their cilia, the first tentacle appearing during the
process of attachment.
In some species the young Actiniæ are seen to pass through their whole
development within the body cavity of the parent. Most anemones are
provided with several circles of more or less cylindrical tentacles, and there
are a few specially beautiful species which, besides tentacles of the usual
form, have, either within or without the ordinary circle of tentacles, lobed or
On account of the ease with which anemones are kept in captivity, their
mode of reproduction can be closely observed. With but few exceptions
they develop from eggs, and in the course of a few weeks are hatched into
ciliated infusorial larvæ, presenting most curious and exquisite
representations of jugs and jars, with cover lids (as seen in Fig. 353, Actinia
effœta). These evince the handiwork of a master hand in the ceramic art.
They are, however, of so translucent a nature as to permit of the internal
structure being seen to consist of nerves and vessels, and which are
rendered more apparent by staining. These settle down in a week or ten
days, and then shed their cilia, the first tentacle appearing during the
process of attachment.
In some species the young Actiniæ are seen to pass through their whole
development within the body cavity of the parent. Most anemones are
provided with several circles of more or less cylindrical tentacles, and there
are a few specially beautiful species which, besides tentacles of the usual
form, have, either within or without the ordinary circle of tentacles, lobed or
Page 614
leaf-like tactile and seizing organs. These belong to the family of the
beautiful Crambactis of the Red Sea. Below these grasping tentacles comes
a circle of thicker arms unlike the former, being spindle shaped. All the
tentacles of the sea-anemones are hollow with a fine aperture at the tip,
through which, on closing rapidly, it is seen to expel a jet of water.
True Corals.—It will have been noticed in the foregoing remarks that in the
soft body-division of the Hexactinia there are both single individuals and
colonies joined together to form stocks. The same diversity in this respect
will be found among corals proper, with this difference, that the skeleton-
forming polyps, by combining, build up substantial structures in the most
secure and advantageous positions. Now it so happens that all the corals
found about our coasts are generally small and solitary dwellers, one of the
best known of which is the scarlet crisp coral, Flabellum, and is
characterised by the slit-like form of the mouth. Viewed sideways it
resembles a small fan fastened along the edges, and just inside a row of
fully developed tentacles is seen protruding. An interesting form of budding
occurs in these corals: the buds fall off, and in this budding condition the
coral might pass, and indeed has been described as a different species of
Flabellum. The colour of the coral is a beautifully transparent red.
Remarkable as the solitary corals are, they are surpassed both in number
and in form by those which form compound stocks, that is to say, in which
the buds do not fall off, but go on building up coral islands and barrier reefs
in the warmer seas. Some very few typical forms only are given in the
group accompanying, shown in Fig. 358.
A different kind of stock is developed in a number of forms, some
producing many buds, as in the Madrepores, in which selected polyps
spring up above the rest, their sides also becoming covered with small buds,
each one of which is a living, feeding, coral animal surrounded by a crown
of tentacles. These Madrepores play a very important part in the building up
of coral reefs.
beautiful Crambactis of the Red Sea. Below these grasping tentacles comes
a circle of thicker arms unlike the former, being spindle shaped. All the
tentacles of the sea-anemones are hollow with a fine aperture at the tip,
through which, on closing rapidly, it is seen to expel a jet of water.
True Corals.—It will have been noticed in the foregoing remarks that in the
soft body-division of the Hexactinia there are both single individuals and
colonies joined together to form stocks. The same diversity in this respect
will be found among corals proper, with this difference, that the skeleton-
forming polyps, by combining, build up substantial structures in the most
secure and advantageous positions. Now it so happens that all the corals
found about our coasts are generally small and solitary dwellers, one of the
best known of which is the scarlet crisp coral, Flabellum, and is
characterised by the slit-like form of the mouth. Viewed sideways it
resembles a small fan fastened along the edges, and just inside a row of
fully developed tentacles is seen protruding. An interesting form of budding
occurs in these corals: the buds fall off, and in this budding condition the
coral might pass, and indeed has been described as a different species of
Flabellum. The colour of the coral is a beautifully transparent red.
Remarkable as the solitary corals are, they are surpassed both in number
and in form by those which form compound stocks, that is to say, in which
the buds do not fall off, but go on building up coral islands and barrier reefs
in the warmer seas. Some very few typical forms only are given in the
group accompanying, shown in Fig. 358.
A different kind of stock is developed in a number of forms, some
producing many buds, as in the Madrepores, in which selected polyps
spring up above the rest, their sides also becoming covered with small buds,
each one of which is a living, feeding, coral animal surrounded by a crown
of tentacles. These Madrepores play a very important part in the building up
of coral reefs.
Page 615
Fig. 354. Developmental stages of Larvæ, Astroides calycularis, × 40.
Another massive coral, the Astroides calycularis, has a different mode of
growth, the tubes not being fused together. When seen standing out these
yellowish-red polyps have been mistaken for small anemones. The larvæ of
this coral leave the egg while still in the large chambered body cavity of the
parent, where they swim about for a time, till they escape through the
mouth. They are worm-like in form, and swim by means of cilia, which are
thicker at the foremost end. The mouth first appears after leaving the parent,
but as they soon become exhausted by the effort they assume a contracted
form, and attach themselves, as do anemones, by pressing the thicker end of
the body against a rock, the whole contracting into a thick round disc, while
longitudinal furrows become visible at the upper part where the mouth sinks
in. At the end of these furrows twelve tentacles appear. The accompanying
illustration shows the various stages through which the larvæ pass in rapid
succession (Fig. 354); at the same time it has already commenced to secrete
its calcareous skeleton. This is not formed as a connected whole but from a
number of separate centres of secretion formed between the polyp and the
substance to which it has attached itself, and which become gradually fused
into a perfect skeleton. A section of the polyp at this stage forms an
interesting microscopical object.
The so-called eight-rayed corals consist of the one genus Tubipora, the
members of which are few in number and not varied in form (Fig. 358, No.
10). In the structure, however, of skeletons they are unique among extant
Another massive coral, the Astroides calycularis, has a different mode of
growth, the tubes not being fused together. When seen standing out these
yellowish-red polyps have been mistaken for small anemones. The larvæ of
this coral leave the egg while still in the large chambered body cavity of the
parent, where they swim about for a time, till they escape through the
mouth. They are worm-like in form, and swim by means of cilia, which are
thicker at the foremost end. The mouth first appears after leaving the parent,
but as they soon become exhausted by the effort they assume a contracted
form, and attach themselves, as do anemones, by pressing the thicker end of
the body against a rock, the whole contracting into a thick round disc, while
longitudinal furrows become visible at the upper part where the mouth sinks
in. At the end of these furrows twelve tentacles appear. The accompanying
illustration shows the various stages through which the larvæ pass in rapid
succession (Fig. 354); at the same time it has already commenced to secrete
its calcareous skeleton. This is not formed as a connected whole but from a
number of separate centres of secretion formed between the polyp and the
substance to which it has attached itself, and which become gradually fused
into a perfect skeleton. A section of the polyp at this stage forms an
interesting microscopical object.
The so-called eight-rayed corals consist of the one genus Tubipora, the
members of which are few in number and not varied in form (Fig. 358, No.
10). In the structure, however, of skeletons they are unique among extant
Page 616
corals. Each individual secretes a smooth-walled tube without calcification
of the vertical septa. These tubes, like the pipes of an organ, stand almost
parallel, and are united to form a stock by means of transverse platforms.
The formation of buds does not appear to take place in this family.
Another of the eight-rayed corals is Gorgoniidæ. These are permanently
fixed to the spot on which they are found, and form a bush-like growth,
giving no idea of the living coral, as it rises in graceful branching colonies,
in deep water, and represents a portion of Gorgonia nobilis with polyps
expanded (Figs. 344 and 358, No. 9).
Other corals present numerous other departures from the types we have
been considering, but so far modified in form as that of the Sea-pen,
Veretillum (Fig. 355), the stock part of which is surrounded by polyps
continued down a portion of the cylindrical stalk. The best known of the
species is Pennatula phosphorea of the Mediterranean.
Pennatulidæ.—This family derives
its name from penna, a quill. Their
spicula also resemble a penholder in
appearance, shown in Fig. 358, No.
3. The polyps are without colour,
provided with eight rather long
retractile tentacula, beautifully
ciliated on the inner aspect with two
series of short processes, and
strengthened by these crystalline
spicula, a row being carried up the
stalk, together with a series of
ciliated processes. The mouth,
occupying the centre of the tentacula,
is somewhat angular. The ova lie
between the membranous part of the
pinnæ; these are globular, of a
yellowish colour, and by pressure
can be made to pass through the
mouth. Dr. Grant wrote:—“A more
of the vertical septa. These tubes, like the pipes of an organ, stand almost
parallel, and are united to form a stock by means of transverse platforms.
The formation of buds does not appear to take place in this family.
Another of the eight-rayed corals is Gorgoniidæ. These are permanently
fixed to the spot on which they are found, and form a bush-like growth,
giving no idea of the living coral, as it rises in graceful branching colonies,
in deep water, and represents a portion of Gorgonia nobilis with polyps
expanded (Figs. 344 and 358, No. 9).
Other corals present numerous other departures from the types we have
been considering, but so far modified in form as that of the Sea-pen,
Veretillum (Fig. 355), the stock part of which is surrounded by polyps
continued down a portion of the cylindrical stalk. The best known of the
species is Pennatula phosphorea of the Mediterranean.
Pennatulidæ.—This family derives
its name from penna, a quill. Their
spicula also resemble a penholder in
appearance, shown in Fig. 358, No.
3. The polyps are without colour,
provided with eight rather long
retractile tentacula, beautifully
ciliated on the inner aspect with two
series of short processes, and
strengthened by these crystalline
spicula, a row being carried up the
stalk, together with a series of
ciliated processes. The mouth,
occupying the centre of the tentacula,
is somewhat angular. The ova lie
between the membranous part of the
pinnæ; these are globular, of a
yellowish colour, and by pressure
can be made to pass through the
mouth. Dr. Grant wrote:—“A more
Page 617
Fig. 355. singular and beautiful spectacle
1. Pennatula phosphorea; 2. Synapta chirodata; could scarcely be conceived than that
3. Anchor-shaped spiculum and plate from the of a deep purple Pennatula
ectoderm of same.
phosphorea, with all its delicate
transparent polyps expanded and
emitting their usual brilliant phosphorescent light, sailing through the still
and dark abyss, by the regular and synchronous pulsations of the minute
fringed arms of the polyps.”
The spicula are seen to be a continuous series of cones fitting into each
other.
Bryozoa, Moss-animals.
The exact position in which the Bryozoa, or moss-animals, should be placed
in the animal kingdom has not been finally determined. They were at one
time associated with corals; then with sponges; but, on further
acquaintance, it became evident that they did not belong to either.
Naturalists also claimed them as Rotifers and Ciliata, but this claim met
with no better reception. Since they appear to have no settled classification,
there can be no objection to linking them once more to corals, as they
apparently resemble these animals by always living in colonies, the
individual members of which are joined in a number of different ways to
form stocks, the individuals themselves, however, being very much smaller
than those of corals proper. The advantage is that the structure of the
Bryozoans can be more readily studied, as many of them live in transparent
chambers or cells, the walls of which, although somewhat firmly
agglutinated together, are flexible enough to fold up, as the animals
instantly withdraw their bodies and close up the top on the slightest alarm
(Fig. 356).
1. Pennatula phosphorea; 2. Synapta chirodata; could scarcely be conceived than that
3. Anchor-shaped spiculum and plate from the of a deep purple Pennatula
ectoderm of same.
phosphorea, with all its delicate
transparent polyps expanded and
emitting their usual brilliant phosphorescent light, sailing through the still
and dark abyss, by the regular and synchronous pulsations of the minute
fringed arms of the polyps.”
The spicula are seen to be a continuous series of cones fitting into each
other.
Bryozoa, Moss-animals.
The exact position in which the Bryozoa, or moss-animals, should be placed
in the animal kingdom has not been finally determined. They were at one
time associated with corals; then with sponges; but, on further
acquaintance, it became evident that they did not belong to either.
Naturalists also claimed them as Rotifers and Ciliata, but this claim met
with no better reception. Since they appear to have no settled classification,
there can be no objection to linking them once more to corals, as they
apparently resemble these animals by always living in colonies, the
individual members of which are joined in a number of different ways to
form stocks, the individuals themselves, however, being very much smaller
than those of corals proper. The advantage is that the structure of the
Bryozoans can be more readily studied, as many of them live in transparent
chambers or cells, the walls of which, although somewhat firmly
agglutinated together, are flexible enough to fold up, as the animals
instantly withdraw their bodies and close up the top on the slightest alarm
(Fig. 356).
Page 618
Fig. 356.—Paludicella, tentacles expanded Fig. 357.—Sea-moss, Flustra, the body
and cell closed. having been withdrawn from its cell.
The general structure of the Bryozoan individual, figured attached by its
footstalk to a stem of wood, consists of a mouth at the anterior part of the
body opening into a muscular pharynx in the alimentary canal, together
occupying a considerable amount of space. The terminal portion turns upon
itself towards the oral opening, its chief attachment being a short strand of
tissue termed the funiculus (shown in Fig. 358, No. 11). In all adults two
masses of cells are found attached to the wall of the chamber; the upper
yields the eggs, within the lower the male elements are developed. Moss-
animals are hermaphrodite, fertilisation being effected by the two elements
mingling together in the body fluid. These are the essential points in the
structure of the whole seventeen hundred species. Among the larger
colonies a number of fresh-water genera are found attached to the roots and
branches of aquatic plants, most of which, however, are inconspicuous. The
and cell closed. having been withdrawn from its cell.
The general structure of the Bryozoan individual, figured attached by its
footstalk to a stem of wood, consists of a mouth at the anterior part of the
body opening into a muscular pharynx in the alimentary canal, together
occupying a considerable amount of space. The terminal portion turns upon
itself towards the oral opening, its chief attachment being a short strand of
tissue termed the funiculus (shown in Fig. 358, No. 11). In all adults two
masses of cells are found attached to the wall of the chamber; the upper
yields the eggs, within the lower the male elements are developed. Moss-
animals are hermaphrodite, fertilisation being effected by the two elements
mingling together in the body fluid. These are the essential points in the
structure of the whole seventeen hundred species. Among the larger
colonies a number of fresh-water genera are found attached to the roots and
branches of aquatic plants, most of which, however, are inconspicuous. The
Page 619
beauty of these minute bodies can only be seen under the microscope. Many
consist of delicate branching growths, the Sea-mats (Flustra), for instance;
others again appear as attractive lace corals, between the open meshes of
which multitudes of minute apertures crowned with tentacles are displayed.
The several individuals of the genus Lepralia are arranged in rows, and
further distinguished by the animals being developed only on one side of
the stock. The marvellous variety of forms presented by these small animals
is in a measure determined by the particular manner of their buddings. The
greater number of fresh-water moss-animals belong to the order
Phylactolæmata, so called because the mouth is provided with a tongue-
shaped lid. The crown of tentacles is furnished with rows of cilia, and is
horseshoe-shaped, the whole being surrounded at its base by an integument
forming a kind of cup, which is either soft or horny. Those belonging to the
wandering types (Cristatella, Plate IV., Nos. 95-98) form flattened elliptical
colonies, some of which creep or move about on a kind of foot. A nervous
system pervades the mass of polyps, while in each separate polyp a nerve
ganglion is seen to be situated between the œsophagus and the posterior
part of the alimentary canal. The colony nerve system regulates the
movements of the stock.
consist of delicate branching growths, the Sea-mats (Flustra), for instance;
others again appear as attractive lace corals, between the open meshes of
which multitudes of minute apertures crowned with tentacles are displayed.
The several individuals of the genus Lepralia are arranged in rows, and
further distinguished by the animals being developed only on one side of
the stock. The marvellous variety of forms presented by these small animals
is in a measure determined by the particular manner of their buddings. The
greater number of fresh-water moss-animals belong to the order
Phylactolæmata, so called because the mouth is provided with a tongue-
shaped lid. The crown of tentacles is furnished with rows of cilia, and is
horseshoe-shaped, the whole being surrounded at its base by an integument
forming a kind of cup, which is either soft or horny. Those belonging to the
wandering types (Cristatella, Plate IV., Nos. 95-98) form flattened elliptical
colonies, some of which creep or move about on a kind of foot. A nervous
system pervades the mass of polyps, while in each separate polyp a nerve
ganglion is seen to be situated between the œsophagus and the posterior
part of the alimentary canal. The colony nerve system regulates the
movements of the stock.
Page 620
Fig. 358.—Typical forms of Corals.
1. Fungia agariciformis; 2. Alcyonium, Cydonium Mulleri; 3. Cydonium, polyps
protruding and tentacles expanded, others closed; 4. A stock viewed from above; 5.
Madrepore abrotanoide; 6. Madrepore, slightly magnified, showing oral opening;
7. Corallidæ; 8. Coral, polyps protruding from cells; 9. Gorgonia nobilis, with
polyps expanded; 10. Tubipora musica; 11. Tubes of same, with polyps expanded,
one cut longitudinally to show internal structure; 12. Sertularia, polyps protruded,
and withdrawn into their polypidoms.
There are many beautifully formed freshwater polyps deserving of more
than a passing notice, as the slender Coryne (Coryne stauridia), found
adhering to the footstalk of a Rhodymenia (Fig. 359), about which it creeps
in the form of a white thread. On placing both under the microscope, the
thread-like body of the little animal appears cylindrical and tubular,
perfectly transparent, and permeated by a central core, apparently cellular in
texture, hollow, and within which a rather slow circulation of globules is
1. Fungia agariciformis; 2. Alcyonium, Cydonium Mulleri; 3. Cydonium, polyps
protruding and tentacles expanded, others closed; 4. A stock viewed from above; 5.
Madrepore abrotanoide; 6. Madrepore, slightly magnified, showing oral opening;
7. Corallidæ; 8. Coral, polyps protruding from cells; 9. Gorgonia nobilis, with
polyps expanded; 10. Tubipora musica; 11. Tubes of same, with polyps expanded,
one cut longitudinally to show internal structure; 12. Sertularia, polyps protruded,
and withdrawn into their polypidoms.
There are many beautifully formed freshwater polyps deserving of more
than a passing notice, as the slender Coryne (Coryne stauridia), found
adhering to the footstalk of a Rhodymenia (Fig. 359), about which it creeps
in the form of a white thread. On placing both under the microscope, the
thread-like body of the little animal appears cylindrical and tubular,
perfectly transparent, and permeated by a central core, apparently cellular in
texture, hollow, and within which a rather slow circulation of globules is
Page 621
perceived. The parent Coryne sends
off numerous branches, the terminal
head of which is oblong, cylindrical,
and at the extreme end there are
arranged four tentacles, long and
slender, each being furnished with a
nodular head. A magnified view of
one detached is shown erect (Fig.
359, No. 2). This polyp is much
infested by parasites, vorticella
growing on it in immense numbers,
forming aggregated clusters here and
there, individuals of the parasitic
colony adhering to each other, and
projecting outwards in every
direction.
Alcyonella, another fresh-water
polyp, is found in the autumn of the
year in all the London Docks
adhering to pieces of floating timber.
A. stagnorum partakes of the
Fig. 359. character of a sponge rather than that
of a polyp. It is usually found in
1. Coryne stauridia; 2. A tentacle detached and gelatinous colonies, and when stood
magnified 200 diameters.
aside for a short time these put forth
a number of ciliated tentacles (shown
in Fig. 360, magnified 100 diameters).
The ova contained within the sac, and viewed by transmitted light, appear
as opaque spheres surrounded by a thin transparent margin; these increase
in thickness as the ova is developed, and such of the ova as lie in contact
seem to unite and form a statoblast. A rapid current in the water around each
animal, drawing with it loose particles and floating animalcules, is seen
moving with some velocity as in other ciliated bodies; and a zone of very
minute vibrating cilia surrounds the transparent margin of each tentacle.
off numerous branches, the terminal
head of which is oblong, cylindrical,
and at the extreme end there are
arranged four tentacles, long and
slender, each being furnished with a
nodular head. A magnified view of
one detached is shown erect (Fig.
359, No. 2). This polyp is much
infested by parasites, vorticella
growing on it in immense numbers,
forming aggregated clusters here and
there, individuals of the parasitic
colony adhering to each other, and
projecting outwards in every
direction.
Alcyonella, another fresh-water
polyp, is found in the autumn of the
year in all the London Docks
adhering to pieces of floating timber.
A. stagnorum partakes of the
Fig. 359. character of a sponge rather than that
of a polyp. It is usually found in
1. Coryne stauridia; 2. A tentacle detached and gelatinous colonies, and when stood
magnified 200 diameters.
aside for a short time these put forth
a number of ciliated tentacles (shown
in Fig. 360, magnified 100 diameters).
The ova contained within the sac, and viewed by transmitted light, appear
as opaque spheres surrounded by a thin transparent margin; these increase
in thickness as the ova is developed, and such of the ova as lie in contact
seem to unite and form a statoblast. A rapid current in the water around each
animal, drawing with it loose particles and floating animalcules, is seen
moving with some velocity as in other ciliated bodies; and a zone of very
minute vibrating cilia surrounds the transparent margin of each tentacle.
Page 622
Dr. Percival Wright discovered on
the western coast of Ireland a new
genus of Alcyonidæ, which he
named after the well-known
naturalist Harte, Hartea elegans
(Plate IV., No. 86). This polyp is
solitary, the body cylindrical, and
fixed by its base to the rock; it has
eight ciliated tentacles, which are
knobbed at their base and most freely
displayed. It is a very beautiful
polyzoon of a clear white colour, and
when fully expanded stands three-
quarters of an inch high.
Lophopus crystallinus (Plate IV., No.
98) displays beautiful plumes of
tentacles arranged in a double
horseshoe-shaped series. When first
Fig. 360.—Alcyonella fluviatella.
observed these polyps resemble in
many respects masses of the water
snail ova, for which they are often mistaken. On placing these jelly-like
masses into a glass trough with some of the clear water taken from the
stream in which they are found, delicate tubes are seen to cautiously
protrude, and the beautiful fringes of cilia are quickly brought into play. The
organisation of L. crystallinus is simple, although it is provided with organs
of digestion, circulation, respiration, and generation. The nervous70 and
muscular systems are well developed. This polyp increases both by budding
and by ova, both of which conditions are shown in Plate IV., No. 98. The
ova are enclosed in the transparent case of the parent. In Lophopus and
some other fresh-water genera, Cristatella, Plumatella, and Alcyonella, the
neural margin of the Lophopore is extended into two triangular arms, giving
it the appearance of a deep crescent.
Another family presents a contrast: there is no lid to the mouth, and the
tentacles are arranged in a circle on a disc. An important rise in organisation
is found in the Gymnolæmata, especially in the lip-mouthed forms; the
the western coast of Ireland a new
genus of Alcyonidæ, which he
named after the well-known
naturalist Harte, Hartea elegans
(Plate IV., No. 86). This polyp is
solitary, the body cylindrical, and
fixed by its base to the rock; it has
eight ciliated tentacles, which are
knobbed at their base and most freely
displayed. It is a very beautiful
polyzoon of a clear white colour, and
when fully expanded stands three-
quarters of an inch high.
Lophopus crystallinus (Plate IV., No.
98) displays beautiful plumes of
tentacles arranged in a double
horseshoe-shaped series. When first
Fig. 360.—Alcyonella fluviatella.
observed these polyps resemble in
many respects masses of the water
snail ova, for which they are often mistaken. On placing these jelly-like
masses into a glass trough with some of the clear water taken from the
stream in which they are found, delicate tubes are seen to cautiously
protrude, and the beautiful fringes of cilia are quickly brought into play. The
organisation of L. crystallinus is simple, although it is provided with organs
of digestion, circulation, respiration, and generation. The nervous70 and
muscular systems are well developed. This polyp increases both by budding
and by ova, both of which conditions are shown in Plate IV., No. 98. The
ova are enclosed in the transparent case of the parent. In Lophopus and
some other fresh-water genera, Cristatella, Plumatella, and Alcyonella, the
neural margin of the Lophopore is extended into two triangular arms, giving
it the appearance of a deep crescent.
Another family presents a contrast: there is no lid to the mouth, and the
tentacles are arranged in a circle on a disc. An important rise in organisation
is found in the Gymnolæmata, especially in the lip-mouthed forms; the
Page 623
individuals belonging to this order vary in structure and fulfil different
physiological functions. There are structures known as zoæcia, stolons,
avicularia, vibracula, and ovicells, some of which are merely modified
individuals. The zoæcia are the normal individuals of the colony, fully
developed for most of the functions of life; the stolons have a much
humbler function, but are indispensable—they are the root-like outgrowths
of the stock, and serve for attaching the colony to foreign objects. The most
remarkable are those known as avicularia, so called because they resemble
the head of a bird. This process acts as a pair of forceps, the large upper
blade of which is very like the skull and upper jaw of a bird, and the smaller
lower blade (like the lower jaw) constantly opens and shuts by means of a
complicated arrangement of muscles (shown in Fig. 361). These avicularia
are movably attached by short muscles to the neck, and are found near the
entrance to a zoæcium. They turn from side to side, snapping in all
directions, catching at every particle of food that may come near; at length
the morsel is drawn into the mouth by the cilia on the tentacles. From this
very peculiar structure the Chilostomata were originally named bird’s-head
corallines, then specifically shepherd’s-purse corallines, Notamia bursaria.
Equally interesting, again, are the vibracula, long thread-like structures,
attached by short footstalks. These keep up a constant whip-like motion, the
object of which is not quite clear. The ovicells, or egg receptacles, are found
at the lower ends of the zoæcia in the form of shields, helmets, or vesicles.
In Plate IV., Nos. 95 and 96, a front and edge view of the statoblast is
shown highly magnified.
physiological functions. There are structures known as zoæcia, stolons,
avicularia, vibracula, and ovicells, some of which are merely modified
individuals. The zoæcia are the normal individuals of the colony, fully
developed for most of the functions of life; the stolons have a much
humbler function, but are indispensable—they are the root-like outgrowths
of the stock, and serve for attaching the colony to foreign objects. The most
remarkable are those known as avicularia, so called because they resemble
the head of a bird. This process acts as a pair of forceps, the large upper
blade of which is very like the skull and upper jaw of a bird, and the smaller
lower blade (like the lower jaw) constantly opens and shuts by means of a
complicated arrangement of muscles (shown in Fig. 361). These avicularia
are movably attached by short muscles to the neck, and are found near the
entrance to a zoæcium. They turn from side to side, snapping in all
directions, catching at every particle of food that may come near; at length
the morsel is drawn into the mouth by the cilia on the tentacles. From this
very peculiar structure the Chilostomata were originally named bird’s-head
corallines, then specifically shepherd’s-purse corallines, Notamia bursaria.
Equally interesting, again, are the vibracula, long thread-like structures,
attached by short footstalks. These keep up a constant whip-like motion, the
object of which is not quite clear. The ovicells, or egg receptacles, are found
at the lower ends of the zoæcia in the form of shields, helmets, or vesicles.
In Plate IV., Nos. 95 and 96, a front and edge view of the statoblast is
shown highly magnified.
Page 624
Fig. 361.
1. Notamia bursaria, shepherd’s-purse Bryozoa; 2. Polyp magnified and
withdrawn into its cell; 3. Portion of a colony of Hydroid polyps.
Another sub-order consists of the Cyclostomata, or round-mouthed
Bryozoans, of which the Tubulipora is the typical form. The stocks are cup-
shaped incrustations, the individuals radiating outwards, as in Plate IV., No.
92. Tubularia dumortierii is a very interesting form, the germinal bodies,
statoblasts, being formed as cell masses on the strand, or funiculus, which
also maintains the stomach in its place. They are round or oval in shape, and
brown or yellow in colour, and consist of two valves fitted one upon the
other like watch glasses, as shown in No. 96. A number of other statoblasts
are shown, Nos. 97, 98, and 99. The edge running round No. 95 is seen to
have barbed tips; the ring itself contains small air chambers, and is termed
1. Notamia bursaria, shepherd’s-purse Bryozoa; 2. Polyp magnified and
withdrawn into its cell; 3. Portion of a colony of Hydroid polyps.
Another sub-order consists of the Cyclostomata, or round-mouthed
Bryozoans, of which the Tubulipora is the typical form. The stocks are cup-
shaped incrustations, the individuals radiating outwards, as in Plate IV., No.
92. Tubularia dumortierii is a very interesting form, the germinal bodies,
statoblasts, being formed as cell masses on the strand, or funiculus, which
also maintains the stomach in its place. They are round or oval in shape, and
brown or yellow in colour, and consist of two valves fitted one upon the
other like watch glasses, as shown in No. 96. A number of other statoblasts
are shown, Nos. 97, 98, and 99. The edge running round No. 95 is seen to
have barbed tips; the ring itself contains small air chambers, and is termed
Page 625
the swimming belt. It is, in fact, a perfect hydrostatic apparatus, giving
support to the winter buds or statoblasts on the surface of the water. The
barbed hooks apparently act as anchors, and by their means they catch on at
points suitable for their development during the coming spring. As soon as
the time comes, the two halves split apart and the germinal mass emerges
forth. Out of these winter buds and statoblasts asexually produced
individuals arise, which reproduce themselves sexually, their descendants
again yielding winter germs. In short, an alternation of generations is a
continually recurring process.
Brachiopoda.—Here again we have to do
with an enigmatical class of arm-footed
animals, of which the Lamp-shells may be
regarded as typical. These have remained
unaltered from the earliest geological
epochs. Brachiopods are divided into two
orders: those having shells without hinges,
and those with shells hinged together. On
the whole they possess less interest for the
microscopists than many other animals,
except in their earliest developmental
stages of existence.
One of the most interesting of the hinge-
class group, living chiefly near the shores
of the warmer seas, is the Lingulidæ. The
valves are almost exactly similar, but are
Fig. 362.—Lingula pyramidata. not hinged together, and have no processes
for the support of the thick fleshy spiral
arms of the animals. In L. pyramidata, found around the Philippine Islands
(Fig. 362), the stalk is nine times longer than the body. The animal does not
attach itself by this, but moves about like a worm, making tubes out of sand,
into which it can withdraw itself and disappear. The cilia at the mantle edge
form a fine sieve, thus preventing foreign particles from entering the gills.
Its internal structure possesses points of interest, and the parasitic growths
covering the cartilaginous structure, miscalled a shell, are curious, and
excite the attention of the naturalist.
support to the winter buds or statoblasts on the surface of the water. The
barbed hooks apparently act as anchors, and by their means they catch on at
points suitable for their development during the coming spring. As soon as
the time comes, the two halves split apart and the germinal mass emerges
forth. Out of these winter buds and statoblasts asexually produced
individuals arise, which reproduce themselves sexually, their descendants
again yielding winter germs. In short, an alternation of generations is a
continually recurring process.
Brachiopoda.—Here again we have to do
with an enigmatical class of arm-footed
animals, of which the Lamp-shells may be
regarded as typical. These have remained
unaltered from the earliest geological
epochs. Brachiopods are divided into two
orders: those having shells without hinges,
and those with shells hinged together. On
the whole they possess less interest for the
microscopists than many other animals,
except in their earliest developmental
stages of existence.
One of the most interesting of the hinge-
class group, living chiefly near the shores
of the warmer seas, is the Lingulidæ. The
valves are almost exactly similar, but are
Fig. 362.—Lingula pyramidata. not hinged together, and have no processes
for the support of the thick fleshy spiral
arms of the animals. In L. pyramidata, found around the Philippine Islands
(Fig. 362), the stalk is nine times longer than the body. The animal does not
attach itself by this, but moves about like a worm, making tubes out of sand,
into which it can withdraw itself and disappear. The cilia at the mantle edge
form a fine sieve, thus preventing foreign particles from entering the gills.
Its internal structure possesses points of interest, and the parasitic growths
covering the cartilaginous structure, miscalled a shell, are curious, and
excite the attention of the naturalist.
Page 626
Another bivalve so unlike a crustacean, among which it has been placed, I
may venture to describe among Lamp-shells. I refer to the barnacle (Lepas)
generally met with covering the bottoms of ships. These, as in the former
genus, are more interesting to the microscopist in the early stage of
existence, and also for the curious parasites known to infest them. The
barnacle protrudes through its two valves six pairs of slender, bristly, two-
branched filamentous limbs, which keep up a constant sweeping motion,
and whereby it secures its supply of food (Fig. 363). When first hatched the
young are in the Nauplius stage, being furnished with a median eye and
three pairs of flagellated appendages. After enjoying a free life the larva
moults and passes into a second stage, in which with its two eyes and
compressed carapace (shown in Fig. 364) it so nearly resembles a Daphnia.
Before these thoracic appendages entirely disappear they first change
places, and then each is seen to be provided with a sucker; by this means
the larva fixes itself to its permanent resting-place, while a cement gland
pours out a secretion that glues it firmly to the point of attachment chosen.
These Cirripedes are not true parasites, inasmuch as they do not extract
nourishment from the body to which they are attached.
One species, the Proteolepas, is in
the adult stage a maggot-like,
limbless, shell-less animal found
living within the mantle chamber of
other members of the same order,
while the root-headed Cirripedes
(Peltogaster curvatus, as Fig. 364,
No. 1) live parasitically upon higher
crustaceans.
Echinodermata.—This sub-kingdom
includes the star-fishes, stone-lilies, Fig. 363.
sea-urchins, feather-stars, and sea- 1. Spat of oyster, some ciliated; 2. Barnacles
cucumbers, some of which have been attached by footstalks.
already alluded to, and are so well
known that they need no lengthy description, while of the fossil sea-urchins
of our chalk formations, the Pentremites and Crinoids, whose silicious
remains are so abundant and so familiar to naturalists and geologists, but
may venture to describe among Lamp-shells. I refer to the barnacle (Lepas)
generally met with covering the bottoms of ships. These, as in the former
genus, are more interesting to the microscopist in the early stage of
existence, and also for the curious parasites known to infest them. The
barnacle protrudes through its two valves six pairs of slender, bristly, two-
branched filamentous limbs, which keep up a constant sweeping motion,
and whereby it secures its supply of food (Fig. 363). When first hatched the
young are in the Nauplius stage, being furnished with a median eye and
three pairs of flagellated appendages. After enjoying a free life the larva
moults and passes into a second stage, in which with its two eyes and
compressed carapace (shown in Fig. 364) it so nearly resembles a Daphnia.
Before these thoracic appendages entirely disappear they first change
places, and then each is seen to be provided with a sucker; by this means
the larva fixes itself to its permanent resting-place, while a cement gland
pours out a secretion that glues it firmly to the point of attachment chosen.
These Cirripedes are not true parasites, inasmuch as they do not extract
nourishment from the body to which they are attached.
One species, the Proteolepas, is in
the adult stage a maggot-like,
limbless, shell-less animal found
living within the mantle chamber of
other members of the same order,
while the root-headed Cirripedes
(Peltogaster curvatus, as Fig. 364,
No. 1) live parasitically upon higher
crustaceans.
Echinodermata.—This sub-kingdom
includes the star-fishes, stone-lilies, Fig. 363.
sea-urchins, feather-stars, and sea- 1. Spat of oyster, some ciliated; 2. Barnacles
cucumbers, some of which have been attached by footstalks.
already alluded to, and are so well
known that they need no lengthy description, while of the fossil sea-urchins
of our chalk formations, the Pentremites and Crinoids, whose silicious
remains are so abundant and so familiar to naturalists and geologists, but
Page 627
little remains to be said. They are chiefly interesting to the microscopist
from their calcareous and silicious appendages, known as spicula. In the
sea-urchin, brittle-star, or feather-star, the outer body surface consists
almost wholly of a deposit of calcium carbonate, combined in the form of
little plates built up into a rigid “test,” whereas in the star-fish it usually
forms a kind of scaffolding, between the layers of which there stretches a
firm leathery skin. Among the sea-cucumbers, the living specimens of
which present extraordinary variations both in form and character, the
deposit consists chiefly of small spicules which grate when the skin is cut
with a knife. If a thin section of the skin is examined under the microscope,
the spicules are seen to be profusely distributed in the middle layer. The
same deposit takes place in the stalked column of a crinoid and in sea-
urchins (Echinodermata), which has tended to preserve them in the
fossilised state. Fig. 365 is selected as exhibiting to perfection the Medusa-
headed Pentacrinoid. This echinoderm differs in two characters: first, its
microscopic structure is that of a meshwork deposited in the spaces of a
network of soft tissue; secondly, that each element, whether a spicule or a
plate, is, despite its trellised structure, deposited around regular lines of
crystallisation (shown in Plate IV., Nos. 89 and 90). Owing to these
characteristics the minutest portion of an echinoderm skeleton is readily
recognised, even when fossilised, under the microscope. Even the species of
the sea-cucumber can be determined by the shape of their spicules.
Another noticeable feature in the radiate structure is that in many cases it
gives to the animal a star-shape, to which the names of star-fish and brittle-
star are given (see Plate IV., No. 91, and Plate XVII., f and n). The ordinary
five-rayed star-fish is found everywhere around the English coasts. This
constant arrangement of organs holds good in the majority of the
echinoderms; it can be detected in the Holothurians, where, beside the
feathery tentacles of the head, rows of shorter sucker-like processes will be
found, which in some instances extend the whole length of the body, the
fixed number of rows being also five in their internal organs. Hence these
animals were formerly grouped under Radiata. But if a sea-cucumber or
sea-urchin be dissected, a marked distinction will be found between them,
in one portion of the organism in particular: the intestine is shut off from the
rest of the body-cavity, often coiling round inside. Examine a star-fish or
sea-urchin on the under-surface of the rays, and, passing in five bands from
from their calcareous and silicious appendages, known as spicula. In the
sea-urchin, brittle-star, or feather-star, the outer body surface consists
almost wholly of a deposit of calcium carbonate, combined in the form of
little plates built up into a rigid “test,” whereas in the star-fish it usually
forms a kind of scaffolding, between the layers of which there stretches a
firm leathery skin. Among the sea-cucumbers, the living specimens of
which present extraordinary variations both in form and character, the
deposit consists chiefly of small spicules which grate when the skin is cut
with a knife. If a thin section of the skin is examined under the microscope,
the spicules are seen to be profusely distributed in the middle layer. The
same deposit takes place in the stalked column of a crinoid and in sea-
urchins (Echinodermata), which has tended to preserve them in the
fossilised state. Fig. 365 is selected as exhibiting to perfection the Medusa-
headed Pentacrinoid. This echinoderm differs in two characters: first, its
microscopic structure is that of a meshwork deposited in the spaces of a
network of soft tissue; secondly, that each element, whether a spicule or a
plate, is, despite its trellised structure, deposited around regular lines of
crystallisation (shown in Plate IV., Nos. 89 and 90). Owing to these
characteristics the minutest portion of an echinoderm skeleton is readily
recognised, even when fossilised, under the microscope. Even the species of
the sea-cucumber can be determined by the shape of their spicules.
Another noticeable feature in the radiate structure is that in many cases it
gives to the animal a star-shape, to which the names of star-fish and brittle-
star are given (see Plate IV., No. 91, and Plate XVII., f and n). The ordinary
five-rayed star-fish is found everywhere around the English coasts. This
constant arrangement of organs holds good in the majority of the
echinoderms; it can be detected in the Holothurians, where, beside the
feathery tentacles of the head, rows of shorter sucker-like processes will be
found, which in some instances extend the whole length of the body, the
fixed number of rows being also five in their internal organs. Hence these
animals were formerly grouped under Radiata. But if a sea-cucumber or
sea-urchin be dissected, a marked distinction will be found between them,
in one portion of the organism in particular: the intestine is shut off from the
rest of the body-cavity, often coiling round inside. Examine a star-fish or
sea-urchin on the under-surface of the rays, and, passing in five bands from
Page 628
top to bottom, a number of small
cylindrical processes are seen gently
waving about; these lie in two rows
with a clear space between them, and
are termed in consequence
ambulacrum. They end in sucker-like
discs, which enable the animal to
attach itself, or pull itself against
strong currents.
Fig. 364.—Parasitic Barnacles.
1. Peltogaster curvatus; 2. Nauplius larva of
Parthenopea; × 200.
cylindrical processes are seen gently
waving about; these lie in two rows
with a clear space between them, and
are termed in consequence
ambulacrum. They end in sucker-like
discs, which enable the animal to
attach itself, or pull itself against
strong currents.
Fig. 364.—Parasitic Barnacles.
1. Peltogaster curvatus; 2. Nauplius larva of
Parthenopea; × 200.
Page 629
Fig. 365.—Medusa-headed Pentacrinoid.
a. Crown and part of stem; b. Upper surface of body, the arms broken away,
showing the food grooves passing to the central mouth.—(Warne.)
Just one other special feature should be noticed: radial canals pass along
under the ambulacra, and join a ring-canal around the mouth, well supplied
by nerve cells.
a. Crown and part of stem; b. Upper surface of body, the arms broken away,
showing the food grooves passing to the central mouth.—(Warne.)
Just one other special feature should be noticed: radial canals pass along
under the ambulacra, and join a ring-canal around the mouth, well supplied
by nerve cells.
Page 630
Fig. 366.
1. Transverse section of a branch of Myriapore; 2, and the others Section of the
stem of Virgularia mirabilis; 3, Spiculum from the outer surface of Sea-pen; 4,
Spicula from Isis hippuris; 5, from Gorgonia elongata; 6, from Alcyonium; 7, and
from Gorgonia umbraculum; 8, Calcareous remains of a Crinoid.
Crinoids (stone-lilies), on the other hand, are formed of a series of flat
rings, pierced through by a narrow canal. The ossicles, as they are termed,
are joined by ligaments passing through their solid substance and endowed
with muscular power; the central part serves for the passage of blood-
vessels, and is surrounded by a sheath of nervous tissue that controls the
movements of the stem, the latter being encrusted by a number of fine
rootlets. The stems possess a limited power of bending. In the words of
Professor Agassiz, “The stem itself passes slowly from a rigid vertical
attitude to a curved or even a drooping position; the cirri move more rapidly
than the arms, and the animal uses them as hooks to catch hold of objects,
and on account of their sharp extremities they are well adapted to retain
their hold of prey.” The rosy-feather star-fish is often found clinging to a
tube of the Sabella worm; the food of crinoids consists of foraminifera,
1. Transverse section of a branch of Myriapore; 2, and the others Section of the
stem of Virgularia mirabilis; 3, Spiculum from the outer surface of Sea-pen; 4,
Spicula from Isis hippuris; 5, from Gorgonia elongata; 6, from Alcyonium; 7, and
from Gorgonia umbraculum; 8, Calcareous remains of a Crinoid.
Crinoids (stone-lilies), on the other hand, are formed of a series of flat
rings, pierced through by a narrow canal. The ossicles, as they are termed,
are joined by ligaments passing through their solid substance and endowed
with muscular power; the central part serves for the passage of blood-
vessels, and is surrounded by a sheath of nervous tissue that controls the
movements of the stem, the latter being encrusted by a number of fine
rootlets. The stems possess a limited power of bending. In the words of
Professor Agassiz, “The stem itself passes slowly from a rigid vertical
attitude to a curved or even a drooping position; the cirri move more rapidly
than the arms, and the animal uses them as hooks to catch hold of objects,
and on account of their sharp extremities they are well adapted to retain
their hold of prey.” The rosy-feather star-fish is often found clinging to a
tube of the Sabella worm; the food of crinoids consists of foraminifera,
Page 631
diatoms, and the larvæ of crustaceans. There are so many curious features in
connection with the Echinodermata that my readers may with advantage
consult “The Challenger Reports” and Warne’s “Natural History” on other
points of interest.
Holothuroidea (sea-cucumbers) are elongated slug-like creatures, the skin
being in structure similar to that of the slug, with a comparatively small
amount of calcareous matter. Usually this occurs in small spicules, which
assume very definite shapes, as the anchors of Synapta (Plate IV., No. 87,
and in Fig. 355). There are also rings of calcareous plates around the gullet,
five of which have the same relation to the radial water-vessels as the
auricles round the jaws of a sea-urchin, and which likewise serve for the
attachment of muscles. These plates are seen in Plate VIII., Nos. 171 and
172, as they appear coloured by selenite films under polarised light. Around
the mouth in Cucumaria is a fringe of branched tentacles connected with the
water-vascular ring; these appear to be used as a net to intercept floating
organisms.
Correlated with the star-fishes is a small family based on the character of
their pincer-like organs, called pedicellariæ, on the surface of the test
(shown in Plate IV., Nos. 93 and 94, magnified × 25). Movable spines cover
the surface of these echinoderms, varying in size from minute bristle-like
structures to long rods. The pedicellariæ are, it is believed, derived from the
smaller spines, and two of them are united at the base by muscles, slightly
curved, and made to approach each other at their extremities. There is a
gradual modification of this type through the whole series. Many uses have
been assigned to them, as the holding of food, as they have been seen to
hold to the fronds of seaweed and keep them steady until the spines and
tube feet can be brought into action. The inner surface of the pedicellariæ
are known to be the most sensitive, and the blades close on the minutest
object touching the inner surface. Beside these peculiar bodies the surface
of the skin has small tubular processes, and tubular feet with suckers at the
end. At the extremity of each arm is a single tube-foot with an impaired
tentacle, and above this again is a small eye coloured by red pigment.
Passing by many other points of interest in the Echinoidæ, the spines are
seen to be attached to the test or shell by a ball and socket joint and well-
connection with the Echinodermata that my readers may with advantage
consult “The Challenger Reports” and Warne’s “Natural History” on other
points of interest.
Holothuroidea (sea-cucumbers) are elongated slug-like creatures, the skin
being in structure similar to that of the slug, with a comparatively small
amount of calcareous matter. Usually this occurs in small spicules, which
assume very definite shapes, as the anchors of Synapta (Plate IV., No. 87,
and in Fig. 355). There are also rings of calcareous plates around the gullet,
five of which have the same relation to the radial water-vessels as the
auricles round the jaws of a sea-urchin, and which likewise serve for the
attachment of muscles. These plates are seen in Plate VIII., Nos. 171 and
172, as they appear coloured by selenite films under polarised light. Around
the mouth in Cucumaria is a fringe of branched tentacles connected with the
water-vascular ring; these appear to be used as a net to intercept floating
organisms.
Correlated with the star-fishes is a small family based on the character of
their pincer-like organs, called pedicellariæ, on the surface of the test
(shown in Plate IV., Nos. 93 and 94, magnified × 25). Movable spines cover
the surface of these echinoderms, varying in size from minute bristle-like
structures to long rods. The pedicellariæ are, it is believed, derived from the
smaller spines, and two of them are united at the base by muscles, slightly
curved, and made to approach each other at their extremities. There is a
gradual modification of this type through the whole series. Many uses have
been assigned to them, as the holding of food, as they have been seen to
hold to the fronds of seaweed and keep them steady until the spines and
tube feet can be brought into action. The inner surface of the pedicellariæ
are known to be the most sensitive, and the blades close on the minutest
object touching the inner surface. Beside these peculiar bodies the surface
of the skin has small tubular processes, and tubular feet with suckers at the
end. At the extremity of each arm is a single tube-foot with an impaired
tentacle, and above this again is a small eye coloured by red pigment.
Passing by many other points of interest in the Echinoidæ, the spines are
seen to be attached to the test or shell by a ball and socket joint and well-
Page 632
arranged muscles, whereby the spines can be moved in any direction. The
tubercles, however, do not cover the whole test, but are disposed chiefly in
five broad zones extending from one pole to another. When a transverse
section of a spine is examined by a medium power it is seen to be made up
of a series of concentric and radiating layers (shown in Plate XVIII., Nos. 1
and 2), the centre being occupied by reticulated structure and structureless
spots arranged at equal distances; these may be termed ribs or pillars.
Passing towards the margin are other rows conveying the impression of a
beautiful indented reticulated tissue. Many of the spines present no
structure, while others exhibit a series of concentric rings of successive
growth, which strongly remind one of the medullary rays of plants. When a
vertical section of a spine is submitted to examination, it is seen to be
composed of cones placed one above the other, the outer margin of each
cone being formed by the series of pillars. In certain species of Echinus the
number of cones is very considerable, while in others there are seldom more
than one or two to be found; from these, transverse sections may when
made show no concentric rings, only the external row of pillars.
The skeleton of echinoderms contains but a small amount of organic matter,
as will be seen on dissolving out the calcareous portion in dilute nitric or
hydrochloric acids. The residuum structure will appear to be meshes or
areolæ, bounded by a substance having a fibrous appearance, intermingled
with granulous matter; in fact, it bears a close resemblance to the areolar
tissue of higher animals, and the test may be considered as formed, not by
the consolidation of the cells of the ectoderm, as in the mollusc, but by the
calcification of the fibro-areolar tissue of the endoderm. This calcification
of a simple fibrous tissue by the deposit of a mineral substance, not in the
meshes of areolæ but in intimate union with the organic basis, is a condition
of much interest to the physiologist; it presents an example of a process
which seems to have an important share in the formation and growth of
bone, namely, in the progressive calcification of the fibrous tissue of the
periosteum membrane covering of the bone.
The development of the sea-urchin from the fertilised egg first divides and
then sub-divides, and in a short time the embryo issues forth with a small
tuft of cilia, by means of which it swims off freely. The larvæ, in its full
tubercles, however, do not cover the whole test, but are disposed chiefly in
five broad zones extending from one pole to another. When a transverse
section of a spine is examined by a medium power it is seen to be made up
of a series of concentric and radiating layers (shown in Plate XVIII., Nos. 1
and 2), the centre being occupied by reticulated structure and structureless
spots arranged at equal distances; these may be termed ribs or pillars.
Passing towards the margin are other rows conveying the impression of a
beautiful indented reticulated tissue. Many of the spines present no
structure, while others exhibit a series of concentric rings of successive
growth, which strongly remind one of the medullary rays of plants. When a
vertical section of a spine is submitted to examination, it is seen to be
composed of cones placed one above the other, the outer margin of each
cone being formed by the series of pillars. In certain species of Echinus the
number of cones is very considerable, while in others there are seldom more
than one or two to be found; from these, transverse sections may when
made show no concentric rings, only the external row of pillars.
The skeleton of echinoderms contains but a small amount of organic matter,
as will be seen on dissolving out the calcareous portion in dilute nitric or
hydrochloric acids. The residuum structure will appear to be meshes or
areolæ, bounded by a substance having a fibrous appearance, intermingled
with granulous matter; in fact, it bears a close resemblance to the areolar
tissue of higher animals, and the test may be considered as formed, not by
the consolidation of the cells of the ectoderm, as in the mollusc, but by the
calcification of the fibro-areolar tissue of the endoderm. This calcification
of a simple fibrous tissue by the deposit of a mineral substance, not in the
meshes of areolæ but in intimate union with the organic basis, is a condition
of much interest to the physiologist; it presents an example of a process
which seems to have an important share in the formation and growth of
bone, namely, in the progressive calcification of the fibrous tissue of the
periosteum membrane covering of the bone.
The development of the sea-urchin from the fertilised egg first divides and
then sub-divides, and in a short time the embryo issues forth with a small
tuft of cilia, by means of which it swims off freely. The larvæ, in its full
Page 633
development, measures about one millimetre in diameter, and is a curious
and remarkable creature.
The sub-kingdom Mollusca comprises some fifty thousand species, and
fresh forms are being constantly discovered, the number of the aquatic
genera being more than double that of the terrestrial species, for it matters
not to what depth of ocean the dredge is let down, some new form is certain
to be gathered. The Challenger expedition has enriched our knowledge of
the deep-sea fauna to an enormous extent; so much so, that fifty volumes
have already been published descriptive of animals brought to the surface.
Nevertheless, we are told that the great coast lines of South America,
Africa, Asia, and parts of Australia have been but imperfectly explored for
smaller kinds of Mollusca.
Molluscs are soft-bodied, cold-blooded animals, without any internal
skeleton, but this is compensated for by the external hardened shell, which
at once serves the purpose of bones, and is a means of defence. These
bodies are not divided into segments like those of worms and insects, but
are enveloped in a muscular covering or skin, termed the mantle, the special
function of which in most species is the formation and secretion of the
shell. The foot, which serves the double purpose of locomotion and
burrowing in the sand or rock, is an organ particularly characteristic of most
molluscs. There are many departures from this rule, as, for instance, in the
group Chitonidæ, where the shell takes the form of a series of eight adjacent
plates; and in another, the Pholadidæ, there are one or more accessory
pieces in addition to the two principal valves. Some are bivalved, others
univalved, and concealed beneath the skin. All shells are mainly composed
of carbonate of lime, with a small admixture of animal matter. Their
microscopic examination reveals a great diversity of structure, as we shall
presently see, and they are accordingly termed porcellaneous, nacreous,
glassy, horny, and fibrous. Most molluscs have the power of repairing
injuries to their shells; many exhibit an outer coat of animal matter, termed
the peristracum, the special function of which is to preserve the shell from
atmospheric and chemical action of the carbonic acid in the water in which
they dwell.
and remarkable creature.
The sub-kingdom Mollusca comprises some fifty thousand species, and
fresh forms are being constantly discovered, the number of the aquatic
genera being more than double that of the terrestrial species, for it matters
not to what depth of ocean the dredge is let down, some new form is certain
to be gathered. The Challenger expedition has enriched our knowledge of
the deep-sea fauna to an enormous extent; so much so, that fifty volumes
have already been published descriptive of animals brought to the surface.
Nevertheless, we are told that the great coast lines of South America,
Africa, Asia, and parts of Australia have been but imperfectly explored for
smaller kinds of Mollusca.
Molluscs are soft-bodied, cold-blooded animals, without any internal
skeleton, but this is compensated for by the external hardened shell, which
at once serves the purpose of bones, and is a means of defence. These
bodies are not divided into segments like those of worms and insects, but
are enveloped in a muscular covering or skin, termed the mantle, the special
function of which in most species is the formation and secretion of the
shell. The foot, which serves the double purpose of locomotion and
burrowing in the sand or rock, is an organ particularly characteristic of most
molluscs. There are many departures from this rule, as, for instance, in the
group Chitonidæ, where the shell takes the form of a series of eight adjacent
plates; and in another, the Pholadidæ, there are one or more accessory
pieces in addition to the two principal valves. Some are bivalved, others
univalved, and concealed beneath the skin. All shells are mainly composed
of carbonate of lime, with a small admixture of animal matter. Their
microscopic examination reveals a great diversity of structure, as we shall
presently see, and they are accordingly termed porcellaneous, nacreous,
glassy, horny, and fibrous. Most molluscs have the power of repairing
injuries to their shells; many exhibit an outer coat of animal matter, termed
the peristracum, the special function of which is to preserve the shell from
atmospheric and chemical action of the carbonic acid in the water in which
they dwell.
Page 634
The shells of gastropods are enlarged with the growth of the mollusc by the
addition of fresh layers to the margin. In some species the periodic
formation of spines occurs; a typical case will be found among Muricidæ.
The varied colours of shells are due to glands situated on the margin of the
mantle, and beneath the peristracum; occasionally the inner layer of
porcellaneous shells is of a different colour to the outer, as, for example, in
the helmet-shells (Cassis), much used by carvers of shell cameos. Light and
warmth, as in the vegetable kingdom, are the great factors in the production
of brilliant colours. In cold climates land snails bury themselves in winter
time in the ground or beneath decaying vegetable matter, and in hot seasons
they close up the aperture of the shells with a temporary lid, called an
epiphragm. These exhibit great tenacity of life, as, for instance, in the
Egyptian desert-snail, Helix desertorum. The reproductive system is in all
cases effected by means of eggs. The ova are usually enclosed in capsules,
and deposited in masses, and the number of eggs contained in the squid and
the whelk have been stated to be thirty or forty thousand. The ova of
molluscs may be gradually developed into the adult, or there may be a free-
swimming ciliated larval stage, or a special larval form, as in the fresh-
water mussel. Most are provided with a more or less distinct head; both
cephalopods and gastropods are furnished with eyes. In land snails these are
found placed on projecting stalks. In most cases the utility of molluscs far
outweighs the injury occasioned by a few species, as, for instance, the
Teredo, and the burrowing habits of the Pholas and Saxicava, compact
marble having been found bored through by them.
Mr. J. Robertson wrote me in 1866:—“Having, while residing here
(Brighton), opportunities of studying the Pholas dactylus, I have
endeavoured during the last six months to discover how this mollusc makes
its hole or crypt in the chalk—by a chemical solvent? by absorption? by
ciliary currents? or by rotatory motions? My observations, dissections, and
experiments set at rest controversy on this point. Between twenty and thirty
of these creatures have been at work in lumps of chalk in sea water in a
finger glass and a pan, at my window for the last three months. The Pholas
dactylus makes its hole by grating the chalk with its rasp-like valves,
licking it up when pulverised with its foot, forcing it up through its
principal or branchial siphon, and squirting it out in oblong nodules. The
crypt protects the Pholas from Conferveæ, often found growing
addition of fresh layers to the margin. In some species the periodic
formation of spines occurs; a typical case will be found among Muricidæ.
The varied colours of shells are due to glands situated on the margin of the
mantle, and beneath the peristracum; occasionally the inner layer of
porcellaneous shells is of a different colour to the outer, as, for example, in
the helmet-shells (Cassis), much used by carvers of shell cameos. Light and
warmth, as in the vegetable kingdom, are the great factors in the production
of brilliant colours. In cold climates land snails bury themselves in winter
time in the ground or beneath decaying vegetable matter, and in hot seasons
they close up the aperture of the shells with a temporary lid, called an
epiphragm. These exhibit great tenacity of life, as, for instance, in the
Egyptian desert-snail, Helix desertorum. The reproductive system is in all
cases effected by means of eggs. The ova are usually enclosed in capsules,
and deposited in masses, and the number of eggs contained in the squid and
the whelk have been stated to be thirty or forty thousand. The ova of
molluscs may be gradually developed into the adult, or there may be a free-
swimming ciliated larval stage, or a special larval form, as in the fresh-
water mussel. Most are provided with a more or less distinct head; both
cephalopods and gastropods are furnished with eyes. In land snails these are
found placed on projecting stalks. In most cases the utility of molluscs far
outweighs the injury occasioned by a few species, as, for instance, the
Teredo, and the burrowing habits of the Pholas and Saxicava, compact
marble having been found bored through by them.
Mr. J. Robertson wrote me in 1866:—“Having, while residing here
(Brighton), opportunities of studying the Pholas dactylus, I have
endeavoured during the last six months to discover how this mollusc makes
its hole or crypt in the chalk—by a chemical solvent? by absorption? by
ciliary currents? or by rotatory motions? My observations, dissections, and
experiments set at rest controversy on this point. Between twenty and thirty
of these creatures have been at work in lumps of chalk in sea water in a
finger glass and a pan, at my window for the last three months. The Pholas
dactylus makes its hole by grating the chalk with its rasp-like valves,
licking it up when pulverised with its foot, forcing it up through its
principal or branchial siphon, and squirting it out in oblong nodules. The
crypt protects the Pholas from Conferveæ, often found growing
Page 635
parasitically not only outside the shell but even within the lips of the valves,
thus preventing the action of the siphons. In the foot there is a spring, or
style, which when removed is found to possess great elasticity, and this
seems to be the mainspring of the motion of the Pholas.”
Fig. 367.—Hexabranchus.
I must pass by many groups and orders to more aberrant types, represented
by the naked-gilled orders, Opisthobranchiata and Nudibranchiata. These
gastropods constitute a large sub-order of extremely beautiful molluscs,
remarkable in shape, and often brilliant in colour. The distinguishing
character of these typical forms consists in the peculiar nature and situation
of their breathing organs, which are exposed on the back of the animal or
around the anterior part, and are not protected by the mantle. But the
situation is varied, and the gills are sometimes placed on each side of the
body, respiration being effected by the ciliated surface of the whole. For
these and other reasons they have been placed in four groups. Nudibranchs
are found in all parts of the world, and are most abundant in depths where
the choicest seaweeds and corallines abound. Their fecundity is very great,
as many as sixty thousand eggs being deposited by a single female at one
time. They are eaten as a luxury where they most abound.
thus preventing the action of the siphons. In the foot there is a spring, or
style, which when removed is found to possess great elasticity, and this
seems to be the mainspring of the motion of the Pholas.”
Fig. 367.—Hexabranchus.
I must pass by many groups and orders to more aberrant types, represented
by the naked-gilled orders, Opisthobranchiata and Nudibranchiata. These
gastropods constitute a large sub-order of extremely beautiful molluscs,
remarkable in shape, and often brilliant in colour. The distinguishing
character of these typical forms consists in the peculiar nature and situation
of their breathing organs, which are exposed on the back of the animal or
around the anterior part, and are not protected by the mantle. But the
situation is varied, and the gills are sometimes placed on each side of the
body, respiration being effected by the ciliated surface of the whole. For
these and other reasons they have been placed in four groups. Nudibranchs
are found in all parts of the world, and are most abundant in depths where
the choicest seaweeds and corallines abound. Their fecundity is very great,
as many as sixty thousand eggs being deposited by a single female at one
time. They are eaten as a luxury where they most abound.
Page 636
Fig. 368.—Longitudinal section of Pleurobranchus aurantiacus, showing
circulation and gills or branchiæ.—(Warne.)
In the Opisthobranchs the branched veins as well as the auricle are placed
behind the ventricle of the heart. They differ from Nudibranchs inasmuch as
they are usually furnished with a pair of tentacles and labial palpi, or an
expansion of the skin like the veil of the larval form. To clearly understand
the character of the internal organisation of these curious animals, the
longitudinal section given in Fig. 368 must be consulted: p is the foot; a the
mouth, covered above with the veil-like expansion, over which are the
tentacles, c; the branchial veins, v, carry the blood to the gills, from which it
flows into the heart at h. This disposition is the opposite of that which
characterises the Prosobranchus. Another anatomical peculiarity, which may
here be referred to, is the direct communication of the system of blood
vessels with the surrounding medium; a characteristic common to most
other molluscs, and on which depends the changeable external appearance
of the animal. In the illustration of Pleurobranchus here given, g indicates
the opening of the duct which conveys water direct to the blood, and
through which the blood vessels permeate the back and foot. Like the holes
in the sponges, it can be filled or emptied at the will of the animal.
Although this, in the main, is the principle of the circulation in most of this
order, one branch possesses no special breathing organs, respiration being
carried on throughout the naked skin of the body.
With regard to the Nudibranchiata, the group having the most symmetrical
form is the extensive family Dorididæ, characterised by differences in the
branchiæ, the relative proportion of the mantle to the foot, and variations in
circulation and gills or branchiæ.—(Warne.)
In the Opisthobranchs the branched veins as well as the auricle are placed
behind the ventricle of the heart. They differ from Nudibranchs inasmuch as
they are usually furnished with a pair of tentacles and labial palpi, or an
expansion of the skin like the veil of the larval form. To clearly understand
the character of the internal organisation of these curious animals, the
longitudinal section given in Fig. 368 must be consulted: p is the foot; a the
mouth, covered above with the veil-like expansion, over which are the
tentacles, c; the branchial veins, v, carry the blood to the gills, from which it
flows into the heart at h. This disposition is the opposite of that which
characterises the Prosobranchus. Another anatomical peculiarity, which may
here be referred to, is the direct communication of the system of blood
vessels with the surrounding medium; a characteristic common to most
other molluscs, and on which depends the changeable external appearance
of the animal. In the illustration of Pleurobranchus here given, g indicates
the opening of the duct which conveys water direct to the blood, and
through which the blood vessels permeate the back and foot. Like the holes
in the sponges, it can be filled or emptied at the will of the animal.
Although this, in the main, is the principle of the circulation in most of this
order, one branch possesses no special breathing organs, respiration being
carried on throughout the naked skin of the body.
With regard to the Nudibranchiata, the group having the most symmetrical
form is the extensive family Dorididæ, characterised by differences in the
branchiæ, the relative proportion of the mantle to the foot, and variations in
Page 637
the radula and jaws. The general aspect of the genus Doris, although drawn
on a small scale, is represented in Plate XVII., Fig. b. The whole sub-order
of Nudibranchs has become more generally known and admired since the
publication of Alder and Hancock’s monograph with its many attractive
coloured illustrations.
These gastropods can be kept alive for some time in a small aquarium if the
precaution is observed of often changing the water and adding a little fresh
seaweed. Numerous curious microscopic forms of life may be found
adhering to them.
Tunicata.—The most remarkable group of animals
belonging to this sub-order are the Ascidians. They
derive their name from the test or tunic, a
membranous consistence, in which they dwell, and
which often includes calcareous spicules. The test has
two orifices, within which is the mantle. Few
microscopic spectacles are more interesting than the Fig. 369.—Aplysia dipilans.
circulation along this network of muslin-like fabric,
and that of the ciliary movement by which the fluid is kept moving. In the
transparent species, as Clavelina and Perophora, the ciliary movement is
seen to greater advantage. The animals are found adhering to the broad
fronds of fuci near low water-mark. They thrive in tanks, and multiply both
by fission and budding. Two species are figured in Plate XVII., Figs. i and
k, the zooids of which were found arranged in clusters, as represented.
Aplysiidæ (sea-hares), so called on account of a slight resemblance to a
crouching hare. The body form is elongated with a partially developed neck
and head, oral and dorsal tentacles, and furnished beneath the mantle with a
shelly plate to protect the branchiæ. The mouth is provided with horny jaws,
and the gizzard is armed with spines, to prepare the food for digestion. The
side lobes are thin and large, and are either folded over the back or used in
swimming. Fig. 369 is a reduced drawing of A. dipilans.
The Pectinibranchs are known as violet sea-snails, Ianthinidæ and
Scalariidæ. The radula consists of numerous rows of pointed teeth arranged
in cross series, forming an angle in the middle. There is no central or
rachidian tooth, and they have thin trochiform shells adapted for a pelagic
on a small scale, is represented in Plate XVII., Fig. b. The whole sub-order
of Nudibranchs has become more generally known and admired since the
publication of Alder and Hancock’s monograph with its many attractive
coloured illustrations.
These gastropods can be kept alive for some time in a small aquarium if the
precaution is observed of often changing the water and adding a little fresh
seaweed. Numerous curious microscopic forms of life may be found
adhering to them.
Tunicata.—The most remarkable group of animals
belonging to this sub-order are the Ascidians. They
derive their name from the test or tunic, a
membranous consistence, in which they dwell, and
which often includes calcareous spicules. The test has
two orifices, within which is the mantle. Few
microscopic spectacles are more interesting than the Fig. 369.—Aplysia dipilans.
circulation along this network of muslin-like fabric,
and that of the ciliary movement by which the fluid is kept moving. In the
transparent species, as Clavelina and Perophora, the ciliary movement is
seen to greater advantage. The animals are found adhering to the broad
fronds of fuci near low water-mark. They thrive in tanks, and multiply both
by fission and budding. Two species are figured in Plate XVII., Figs. i and
k, the zooids of which were found arranged in clusters, as represented.
Aplysiidæ (sea-hares), so called on account of a slight resemblance to a
crouching hare. The body form is elongated with a partially developed neck
and head, oral and dorsal tentacles, and furnished beneath the mantle with a
shelly plate to protect the branchiæ. The mouth is provided with horny jaws,
and the gizzard is armed with spines, to prepare the food for digestion. The
side lobes are thin and large, and are either folded over the back or used in
swimming. Fig. 369 is a reduced drawing of A. dipilans.
The Pectinibranchs are known as violet sea-snails, Ianthinidæ and
Scalariidæ. The radula consists of numerous rows of pointed teeth arranged
in cross series, forming an angle in the middle. There is no central or
rachidian tooth, and they have thin trochiform shells adapted for a pelagic
Page 638
life. They are mostly of a violet colour, from which they derive their name,
the colour being more vivid on the underside, which is turned up towards
the light when the animal is swimming near the surface of the sea (Fig.
370).
Fig. 370.—Ianthinia, Violet Sea-snail.—(Warne.)
The bubble b, drawn somewhat too large, is about to be joined to the anterior end
of the float; c. Shell; l. Float; p. Foot; t. Head.
The most interesting feature in connection with these oceanic snails is the
curious float which they construct to support their egg-capsules. It is a
gelatinous raft, in fact, enclosing air-bubbles, which is attached to the foot,
the egg capsules being suspended from its under-surface. They are unable to
sink so long as they are in connection with their floats, and are therefore
the colour being more vivid on the underside, which is turned up towards
the light when the animal is swimming near the surface of the sea (Fig.
370).
Fig. 370.—Ianthinia, Violet Sea-snail.—(Warne.)
The bubble b, drawn somewhat too large, is about to be joined to the anterior end
of the float; c. Shell; l. Float; p. Foot; t. Head.
The most interesting feature in connection with these oceanic snails is the
curious float which they construct to support their egg-capsules. It is a
gelatinous raft, in fact, enclosing air-bubbles, which is attached to the foot,
the egg capsules being suspended from its under-surface. They are unable to
sink so long as they are in connection with their floats, and are therefore
Page 639
often cast on shore during storms, and furnish an endless series of
microscopic specimens. The violet snails feed on various kinds of jelly-fish,
and occur in shoals.
Pond Snails.—The three families, Limnœidæ, Physidæ, and Chilinidæ,
form a special group of the pulminate, sessile-eyed fresh-water snails. The
larger family of these belongs to the genus Limnœa, having a compressed
and triangular head with two tentacles and eyes placed at their inner base.
They are prolific and gregarious, and their ova are enclosed in transparent
gelatinous capsules, deposited in continuous series, and firmly glued to
submerged stems and leaves of aquatic plants. L. stagnalis is common in all
ponds, marshes and slow-running rivers of Great Britain.
Fig. 371.—Ova and young of Limnæus stagnalis.
One of the species, L. trancatula, is the host of the liver-fluke so fatal to
sheep. The fluke parasite passes one stage of its existence in the intestine of
the pond snail.
Each ova-sac of Limnœa contains from fifty to sixty ova (represented in
Fig. 371, at a). If examined with a low power soon after the eggs are
deposited, they appear to consist simply of a pellucid protoplasmic
substance. In about twenty-four hours a very minute yellowish spot, the
nucleus, is discovered near the cell-wall. In another twenty-four hours the
microscopic specimens. The violet snails feed on various kinds of jelly-fish,
and occur in shoals.
Pond Snails.—The three families, Limnœidæ, Physidæ, and Chilinidæ,
form a special group of the pulminate, sessile-eyed fresh-water snails. The
larger family of these belongs to the genus Limnœa, having a compressed
and triangular head with two tentacles and eyes placed at their inner base.
They are prolific and gregarious, and their ova are enclosed in transparent
gelatinous capsules, deposited in continuous series, and firmly glued to
submerged stems and leaves of aquatic plants. L. stagnalis is common in all
ponds, marshes and slow-running rivers of Great Britain.
Fig. 371.—Ova and young of Limnæus stagnalis.
One of the species, L. trancatula, is the host of the liver-fluke so fatal to
sheep. The fluke parasite passes one stage of its existence in the intestine of
the pond snail.
Each ova-sac of Limnœa contains from fifty to sixty ova (represented in
Fig. 371, at a). If examined with a low power soon after the eggs are
deposited, they appear to consist simply of a pellucid protoplasmic
substance. In about twenty-four hours a very minute yellowish spot, the
nucleus, is discovered near the cell-wall. In another twenty-four hours the
Page 640
nucleus referred to is seen to have assumed a somewhat deeper colour and
to contain within it a minute spot—a nucleolus.
On the fourth day the nucleus has changed its position, and is enlarged to
double the size; a slightly magnified view is seen at b. On a closer
examination a tranverse fissure is seen; this on the eighth day divides the
small mass as at c, and the outer wall is thickened. The embryo becomes
detached from the side of the cell, and moves with a rotatory motion around
the interior; the direction of this motion is from the right to the left, and is
always increased when sunlight falls upon it. The increase is gradual up to
the eighteenth day, when the changes are more distinctly visible, and the
ova crowd down to the mouth of the ova-sac, as at d. By employing a
higher magnifying power a minute black spec, the future eye (e) and
tentacles of the snail, is quite visible. Upon closely observing it, a fringe of
cilia is noticed in motion near the edge of the shell. It is now apparent that
the rotatory motion first observed must have been in a great measure due to
this; and the current kept up in the fluid contents of the cell by the ciliary
fringes. For days after the young animal has escaped from the egg, this
ciliary motion is carried on, not alone by the fringe surrounding the mouth,
but by cilia entirely surrounding the tentacles themselves, which whips up a
supply of nourishment, and at the same time aeration of the blood is
effected. From the twenty-sixth to the twenty-eighth day it appears actively
engaged near the side of the egg, using force to break through the cell-wall,
which at length it succeeds in accomplishing; leaving its shell in the ova-
sac, and immediately attaching itself to the side of the glass its ciliary action
recommences, and it appears to have advanced a stage, as at f. It is still
some months before the embryo grows to the perfect form, Fig. 372; the
animal is here shown with its sucker-like foot adhering closely to the glass
of the aquarium. A single snail will deposit from two to three of these ova-
sacs a week, producing, in the course of six weeks or two months, from 900
to 1,000 young.
The shell itself is deposited in minute cells, which take up a circular
position around the axis; on its under-surface a hyaline membrane is
secreted. The integument expands, and at various points an internal
colouring-matter or pigment is deposited. The increase of the animal goes
on until the expanded foot is formed, the outer edge of which is rounded off
to contain within it a minute spot—a nucleolus.
On the fourth day the nucleus has changed its position, and is enlarged to
double the size; a slightly magnified view is seen at b. On a closer
examination a tranverse fissure is seen; this on the eighth day divides the
small mass as at c, and the outer wall is thickened. The embryo becomes
detached from the side of the cell, and moves with a rotatory motion around
the interior; the direction of this motion is from the right to the left, and is
always increased when sunlight falls upon it. The increase is gradual up to
the eighteenth day, when the changes are more distinctly visible, and the
ova crowd down to the mouth of the ova-sac, as at d. By employing a
higher magnifying power a minute black spec, the future eye (e) and
tentacles of the snail, is quite visible. Upon closely observing it, a fringe of
cilia is noticed in motion near the edge of the shell. It is now apparent that
the rotatory motion first observed must have been in a great measure due to
this; and the current kept up in the fluid contents of the cell by the ciliary
fringes. For days after the young animal has escaped from the egg, this
ciliary motion is carried on, not alone by the fringe surrounding the mouth,
but by cilia entirely surrounding the tentacles themselves, which whips up a
supply of nourishment, and at the same time aeration of the blood is
effected. From the twenty-sixth to the twenty-eighth day it appears actively
engaged near the side of the egg, using force to break through the cell-wall,
which at length it succeeds in accomplishing; leaving its shell in the ova-
sac, and immediately attaching itself to the side of the glass its ciliary action
recommences, and it appears to have advanced a stage, as at f. It is still
some months before the embryo grows to the perfect form, Fig. 372; the
animal is here shown with its sucker-like foot adhering closely to the glass
of the aquarium. A single snail will deposit from two to three of these ova-
sacs a week, producing, in the course of six weeks or two months, from 900
to 1,000 young.
The shell itself is deposited in minute cells, which take up a circular
position around the axis; on its under-surface a hyaline membrane is
secreted. The integument expands, and at various points an internal
colouring-matter or pigment is deposited. The increase of the animal goes
on until the expanded foot is formed, the outer edge of which is rounded off
Page 641
and turned over by condensed tissue in
the form of a twisted wire; this encloses a
network of small vessels filled with a
fluid in constant and rapid motion. The
course of the blood or fluid, as it passes
from the heart, may be traced through the
larger branches to the respiratory organs,
consisting of branchial-fringes placed
near the mouth; the blood may also be
seen returning through other vessels. The
heart, a strong muscular apparatus, is
pear-shaped, and enclosed within a
pericardium or extremely thin and
pellucid enveloping membrane. The heart
is seen to be furnished with muscular
bands of considerable strength, the action
of which appears like the alternate to-
and-fro motion occasioned by drawing
Fig. 372.—Limnæus stagnalis (natural size).
out a band of indiarubber, and which,
although so minute, are clearly analogous
to the muscular fibres of the mammal heart; it beats or contracts at the rate
of about sixty times a minute, and is placed rather far back in the body,
towards the axis of the shell. The nervous system is made up of ganglia, or
nervous centres, and distributed throughout the various portions of the
body.
The singular arrangement of the eye cannot be omitted; it appears at an
early stage of life to be within the tentacle, and consequently capable of
being retracted into it. In the adult animal the eye is situated at the base of
the tentacle; and although it can be protruded at pleasure for a short
distance, it seems to depend much upon the tentacle for protection as a
coverlid—it invariably draws down the tentacle over the eye when that
organ needs protection. The eye itself is pyriform, somewhat resembling the
round figure of the human eye-ball, with its optic-nerve attached. In colour
it is very dark, having a central pupillary-opening for the admission of light.
The tentacle, which is cylindrical in the young animal, becomes flat and
triangular in shape in the adult. The tentacles serve in some respect to
the form of a twisted wire; this encloses a
network of small vessels filled with a
fluid in constant and rapid motion. The
course of the blood or fluid, as it passes
from the heart, may be traced through the
larger branches to the respiratory organs,
consisting of branchial-fringes placed
near the mouth; the blood may also be
seen returning through other vessels. The
heart, a strong muscular apparatus, is
pear-shaped, and enclosed within a
pericardium or extremely thin and
pellucid enveloping membrane. The heart
is seen to be furnished with muscular
bands of considerable strength, the action
of which appears like the alternate to-
and-fro motion occasioned by drawing
Fig. 372.—Limnæus stagnalis (natural size).
out a band of indiarubber, and which,
although so minute, are clearly analogous
to the muscular fibres of the mammal heart; it beats or contracts at the rate
of about sixty times a minute, and is placed rather far back in the body,
towards the axis of the shell. The nervous system is made up of ganglia, or
nervous centres, and distributed throughout the various portions of the
body.
The singular arrangement of the eye cannot be omitted; it appears at an
early stage of life to be within the tentacle, and consequently capable of
being retracted into it. In the adult animal the eye is situated at the base of
the tentacle; and although it can be protruded at pleasure for a short
distance, it seems to depend much upon the tentacle for protection as a
coverlid—it invariably draws down the tentacle over the eye when that
organ needs protection. The eye itself is pyriform, somewhat resembling the
round figure of the human eye-ball, with its optic-nerve attached. In colour
it is very dark, having a central pupillary-opening for the admission of light.
The tentacle, which is cylindrical in the young animal, becomes flat and
triangular in shape in the adult. The tentacles serve in some respect to
Page 642
distinguish species. In Limnœa they are, as I have said, compressed and
triangular, with the eyes at their inner base. In Physa they are cylindrical
and slender and without lateral mantle lobes. The development of the
lingual membrane is delayed; consequently, the young animal does not
early take to a vegetable sustenance: in place of teeth it has two rows of
cilia, as before stated, which drop off when the teeth are fully formed. The
lingual band bearing the teeth, or the “tongue,” as it is termed, consists of
several rows of cutting spines, pointed with silica.
It is a fact of some interest, physiologically, to know that if the young
animal is kept in fresh water alone, without vegetable matter of any kind, it
retains its cilia, and arrest of development follows, and it more slowly
acquires gastric teeth, and attains to perfection in form or size. If, at the
same time, it is confined within a narrow cell or space, it grows only to such
a size as will enable it to move about freely; thus it is made to adapt itself to
the necessities of a restricted state of existence. Some young animals in a
narrow glass-cell, at the end of six months, were alive and well; the cilia
were seen to be retained around the tentacles in constant activity, whilst
other animals of the same brood and age, placed in a situation favourable to
growth, attained their full size, and produced young, which grew in three
weeks to the size of their elder relations.71
My experimental investigations were further extended to the development
of the lingual membrane, or teeth, of Gastropoda, as well as the jaw and
radula. In Limnœa, the teeth when fully developed resemble those of Helix;
that is to say, in the fully grown animal are found several rows or bands of
similar teeth, with simple obtuse cusps and a much suppressed central tooth.
In the young snail a high power of the microscope is required to make them
out. The dental band, however, in most Mollusca is disposed in longitudinal
series, but varies a good deal in this respect, as will be seen on reference to
my several papers, with illustrations of upwards of a hundred different
species, published in “Linnæan Transactions” of 1866, and in the
“Microscopical Society’s Transactions” of 1868. By way of example I may
say, in the Pulmonata the lingual band usually consists of a single median
row, the laterals on each side being broad and similar. But in many other
groups the teeth are arranged in three, five, or seven dissimilar series.
Taking Nerita as a type, the broad teeth on each side of the median are
triangular, with the eyes at their inner base. In Physa they are cylindrical
and slender and without lateral mantle lobes. The development of the
lingual membrane is delayed; consequently, the young animal does not
early take to a vegetable sustenance: in place of teeth it has two rows of
cilia, as before stated, which drop off when the teeth are fully formed. The
lingual band bearing the teeth, or the “tongue,” as it is termed, consists of
several rows of cutting spines, pointed with silica.
It is a fact of some interest, physiologically, to know that if the young
animal is kept in fresh water alone, without vegetable matter of any kind, it
retains its cilia, and arrest of development follows, and it more slowly
acquires gastric teeth, and attains to perfection in form or size. If, at the
same time, it is confined within a narrow cell or space, it grows only to such
a size as will enable it to move about freely; thus it is made to adapt itself to
the necessities of a restricted state of existence. Some young animals in a
narrow glass-cell, at the end of six months, were alive and well; the cilia
were seen to be retained around the tentacles in constant activity, whilst
other animals of the same brood and age, placed in a situation favourable to
growth, attained their full size, and produced young, which grew in three
weeks to the size of their elder relations.71
My experimental investigations were further extended to the development
of the lingual membrane, or teeth, of Gastropoda, as well as the jaw and
radula. In Limnœa, the teeth when fully developed resemble those of Helix;
that is to say, in the fully grown animal are found several rows or bands of
similar teeth, with simple obtuse cusps and a much suppressed central tooth.
In the young snail a high power of the microscope is required to make them
out. The dental band, however, in most Mollusca is disposed in longitudinal
series, but varies a good deal in this respect, as will be seen on reference to
my several papers, with illustrations of upwards of a hundred different
species, published in “Linnæan Transactions” of 1866, and in the
“Microscopical Society’s Transactions” of 1868. By way of example I may
say, in the Pulmonata the lingual band usually consists of a single median
row, the laterals on each side being broad and similar. But in many other
groups the teeth are arranged in three, five, or seven dissimilar series.
Taking Nerita as a type, the broad teeth on each side of the median are
Page 643
termed laterals; and the numerous small teeth on the outside of the band,
known as the pleuræ, are termed uncini.
Since the investigations of Lovén into the lingual dentition of the Mollusca,
various observers have studied the subject, with great advantage to our
knowledge of the affinities of these animals. That these investigations have
proved of value is shown by the light which has been shed on the true
position of many species. When once we have ascertained the homology of
a genus, whose relations were otherwise somewhat doubtful, it is surprising
how other characteristics, even of the shell, probably misunderstood before,
concur to bear out the affinities indicated by the lingual band. These tooth-
bearing membranes, armed with sharp cutting points, admirably adapted for
the division of the food on which they feed, are most of them beautiful
objects for the microscope.
Fig. 373.
1. Palate of Buccinum undatum, common Whelk, seen under polarised light; 2.
Palate of Doris tuberculata, Sea-slug.
The two ends of each longitudinal row of teeth are connected with muscles
attached to the upper and lower surfaces of cartilaginous cushions; the
alternate contractions and extensions of the muscles cause the bands of
teeth to work backwards and forwards, after the fashion of a chain-saw, or
rather of a rasp, upon any substance to which it is applied, and the resulting
wear and tear of the anterior teeth are made good by a development of new
teeth in the secreting sac in which the hinder end of the band is lodged.
Besides the chain-saw-like motion of the band the lingual membrane has a
known as the pleuræ, are termed uncini.
Since the investigations of Lovén into the lingual dentition of the Mollusca,
various observers have studied the subject, with great advantage to our
knowledge of the affinities of these animals. That these investigations have
proved of value is shown by the light which has been shed on the true
position of many species. When once we have ascertained the homology of
a genus, whose relations were otherwise somewhat doubtful, it is surprising
how other characteristics, even of the shell, probably misunderstood before,
concur to bear out the affinities indicated by the lingual band. These tooth-
bearing membranes, armed with sharp cutting points, admirably adapted for
the division of the food on which they feed, are most of them beautiful
objects for the microscope.
Fig. 373.
1. Palate of Buccinum undatum, common Whelk, seen under polarised light; 2.
Palate of Doris tuberculata, Sea-slug.
The two ends of each longitudinal row of teeth are connected with muscles
attached to the upper and lower surfaces of cartilaginous cushions; the
alternate contractions and extensions of the muscles cause the bands of
teeth to work backwards and forwards, after the fashion of a chain-saw, or
rather of a rasp, upon any substance to which it is applied, and the resulting
wear and tear of the anterior teeth are made good by a development of new
teeth in the secreting sac in which the hinder end of the band is lodged.
Besides the chain-saw-like motion of the band the lingual membrane has a
Page 644
kind of licking or scraping action as a whole. With the constant growth of
the band new teeth are developed, when the teeth on the extreme portion of
the band differ much in size and form from those in the median line.
As I have shown in the papers already referred to, that as each row is a
repetition of the first, the arrangement of teeth admits of easy representation
by a numerical formula, in which, when the uncini are very numerous, they
are indicated by the sign ∞ (infinity), and the others by the proper figure.
Thus, ∞ · 5 · 1 · 5 · ∞, which, in the genus Trochus, signifies that each row
consists of one median, flanked on both sides by five lateral teeth, and these
again by a large number of uncini. When only three areas are found, the
outer ones must be considered the pleuræ, inasmuch as there is frequently a
manifest division in the membrane between them and the lateral areas.
Most of the Cephalopod molluscs are provided with well-developed teeth,
and they are, as we know, carnivorous. The teeth of the cuttle-fish, Sepia
officinalis (Plate V., No. 111), resemble those of the Pteropoda, and have the
same formula, 3 · 1 · 3. Sepia are also furnished with a retractile proboscis,
and a prehensile spiny collar, apparently for the purpose of seizing and
holding prey while the teeth are tearing it to pieces. In the squid Loligo
(Plate V., No. 113) the median teeth are broad at the base, approach the
tricuspid form with a prolonged acute central cusp, while the uncini are
much prolonged and slightly curved. The lingual band increases in breadth
towards the base, sometimes to twice that of the anterior portion. This band,
mounted dry, forms an attractive object for black-ground illumination.
In another family, that of the rock-limpet, Patella radiata, the lingual band
(Plate V., No. 116) well serves to distinguish it from the better-known
common limpet. It is furnished with a remarkable long ribbon, studded by
numerous rows of strong dark-brown tricuspid teeth. The lingual membrane
when not in use lies folded up in the abdominal cavity. The teeth of Acmæa
are somewhat differently arranged (Plate V., No. 117); their formula is 3 · 1
· 3.
Testacella maugei, belonging to Pulmonifera, is slug-like in appearance,
and subterranean in its habits, chiefly feeding on earth-worms. During
winter and in dry weather it forms a kind of cocoon, and thus completely
encloses itself in an opaque white mantle; in this way it protects itself from
the band new teeth are developed, when the teeth on the extreme portion of
the band differ much in size and form from those in the median line.
As I have shown in the papers already referred to, that as each row is a
repetition of the first, the arrangement of teeth admits of easy representation
by a numerical formula, in which, when the uncini are very numerous, they
are indicated by the sign ∞ (infinity), and the others by the proper figure.
Thus, ∞ · 5 · 1 · 5 · ∞, which, in the genus Trochus, signifies that each row
consists of one median, flanked on both sides by five lateral teeth, and these
again by a large number of uncini. When only three areas are found, the
outer ones must be considered the pleuræ, inasmuch as there is frequently a
manifest division in the membrane between them and the lateral areas.
Most of the Cephalopod molluscs are provided with well-developed teeth,
and they are, as we know, carnivorous. The teeth of the cuttle-fish, Sepia
officinalis (Plate V., No. 111), resemble those of the Pteropoda, and have the
same formula, 3 · 1 · 3. Sepia are also furnished with a retractile proboscis,
and a prehensile spiny collar, apparently for the purpose of seizing and
holding prey while the teeth are tearing it to pieces. In the squid Loligo
(Plate V., No. 113) the median teeth are broad at the base, approach the
tricuspid form with a prolonged acute central cusp, while the uncini are
much prolonged and slightly curved. The lingual band increases in breadth
towards the base, sometimes to twice that of the anterior portion. This band,
mounted dry, forms an attractive object for black-ground illumination.
In another family, that of the rock-limpet, Patella radiata, the lingual band
(Plate V., No. 116) well serves to distinguish it from the better-known
common limpet. It is furnished with a remarkable long ribbon, studded by
numerous rows of strong dark-brown tricuspid teeth. The lingual membrane
when not in use lies folded up in the abdominal cavity. The teeth of Acmæa
are somewhat differently arranged (Plate V., No. 117); their formula is 3 · 1
· 3.
Testacella maugei, belonging to Pulmonifera, is slug-like in appearance,
and subterranean in its habits, chiefly feeding on earth-worms. During
winter and in dry weather it forms a kind of cocoon, and thus completely
encloses itself in an opaque white mantle; in this way it protects itself from
Page 645
frost and cold. Its lingual membrane is large, and covered with about fifty
rows of divergent teeth, gradually diminishing in size towards the median
row; each tooth is barbed and pointed, broader towards the base, and with
an articulating nipple set in the basement membrane. A few rows are
represented slightly magnified (Plate V., No. 121). Their formula is 0 0 · 1 ·
0 0.
Tongues, etc., of Gasteropods.
Tuffen West, del. W. F. Maples, ad. nat. del. Edmund Evans.
Plate V.
The boat-shell, Cymba olla, belonging to the Velutinidæ, formula 0 · 1 · 0,
or 1 · 1 · 1. The lingual band (Plate V., No. 118) is narrow and ribbon-like
in its appearance, with numerous trident-shaped teeth set on a strong
rows of divergent teeth, gradually diminishing in size towards the median
row; each tooth is barbed and pointed, broader towards the base, and with
an articulating nipple set in the basement membrane. A few rows are
represented slightly magnified (Plate V., No. 121). Their formula is 0 0 · 1 ·
0 0.
Tongues, etc., of Gasteropods.
Tuffen West, del. W. F. Maples, ad. nat. del. Edmund Evans.
Plate V.
The boat-shell, Cymba olla, belonging to the Velutinidæ, formula 0 · 1 · 0,
or 1 · 1 · 1. The lingual band (Plate V., No. 118) is narrow and ribbon-like
in its appearance, with numerous trident-shaped teeth set on a strong
Page 646
muscular membrane. The end of the band and its connection with the
muscles at the extremity of the cartilaginous cushion is shown in the
drawing. The blueish appearance is produced by a selenite film and
polarised light. In Scapander ligniarius the band (Plate V., No. 119) is also
narrow, but the teeth are bold and of extraordinary size; their formula is 1 ·
0 · 1. This mollusc is said to be eyeless. Pleurobranchus plumula belongs to
the same family; its teeth are simple, recurved, and convex, and arranged in
numerous divergent rows, the medians of which are largest. The mandible
(Plate V., No. 122) presents an exceedingly pretty tesselated appearance,
and the numerous divergent rows of teeth are tricuspid.
The velvety-shell, Velutina lævigata, formula 3 · 1 · 3. The teeth (Plate V.,
No. 108) are small and fine; medians recurved, with a series of delicate
denticulations on either side of the central cusp, which is much prolonged:
1st laterals, denticulate, with outer cusp prolonged; 2nd and 3rd laterals,
simple curved or hooked-shaped. The mandible (No. 109), divided in the
centre, forms two plates of divergent denticulations.
The ear-shell, Haliotis tuberculatus, is a well-known beautiful shell, much
used for ornamental purposes. The lingual band (Plate V., No. 114), is well
developed. The medians are flattened-out, recurved obtuse teeth; 1st
laterals, trapezoidal or beam-like; uncini numerous, about sixty, denticulate,
the few first pairs prolonged into strong pointed cusps.
The top-shell, Turbo marmoratus. After the outer layer of shell is removed,
it presents a delicate pearly appearance. Its lingual band (No. 123) closely
resembles Trochus; it is long and narrow, the median teeth are broadest,
with five recurved laterals, and numerous rows of uncini, slender and
hooked. A single row only is represented in the plate.
Cyclotus translucidus, a family of operculate land-shells, belongs to the
Cyclostomatidæ. The teeth shown in No. 110, formula 3 · 1 · 3, are
arranged in slightly divergent rows on a narrow band; they are more or less
subquadrate, recurved, with their central cusps prolonged. Cistula catenata,
one of the family Cyclophoridæ; its band (No. 115) formula, 2 · 1 · 2. Its
teeth resemble those of Littorina. The lingual band of Cyclostomatidæ
points out a near alliance to the Trochidæ; but this question can only be
determined by an examination of several species, when it may, perhaps, be
muscles at the extremity of the cartilaginous cushion is shown in the
drawing. The blueish appearance is produced by a selenite film and
polarised light. In Scapander ligniarius the band (Plate V., No. 119) is also
narrow, but the teeth are bold and of extraordinary size; their formula is 1 ·
0 · 1. This mollusc is said to be eyeless. Pleurobranchus plumula belongs to
the same family; its teeth are simple, recurved, and convex, and arranged in
numerous divergent rows, the medians of which are largest. The mandible
(Plate V., No. 122) presents an exceedingly pretty tesselated appearance,
and the numerous divergent rows of teeth are tricuspid.
The velvety-shell, Velutina lævigata, formula 3 · 1 · 3. The teeth (Plate V.,
No. 108) are small and fine; medians recurved, with a series of delicate
denticulations on either side of the central cusp, which is much prolonged:
1st laterals, denticulate, with outer cusp prolonged; 2nd and 3rd laterals,
simple curved or hooked-shaped. The mandible (No. 109), divided in the
centre, forms two plates of divergent denticulations.
The ear-shell, Haliotis tuberculatus, is a well-known beautiful shell, much
used for ornamental purposes. The lingual band (Plate V., No. 114), is well
developed. The medians are flattened-out, recurved obtuse teeth; 1st
laterals, trapezoidal or beam-like; uncini numerous, about sixty, denticulate,
the few first pairs prolonged into strong pointed cusps.
The top-shell, Turbo marmoratus. After the outer layer of shell is removed,
it presents a delicate pearly appearance. Its lingual band (No. 123) closely
resembles Trochus; it is long and narrow, the median teeth are broadest,
with five recurved laterals, and numerous rows of uncini, slender and
hooked. A single row only is represented in the plate.
Cyclotus translucidus, a family of operculate land-shells, belongs to the
Cyclostomatidæ. The teeth shown in No. 110, formula 3 · 1 · 3, are
arranged in slightly divergent rows on a narrow band; they are more or less
subquadrate, recurved, with their central cusps prolonged. Cistula catenata,
one of the family Cyclophoridæ; its band (No. 115) formula, 2 · 1 · 2. Its
teeth resemble those of Littorina. The lingual band of Cyclostomatidæ
points out a near alliance to the Trochidæ; but this question can only be
determined by an examination of several species, when it may, perhaps, be
Page 647
decided to give them rank as a sub-order. They are numerous enough; the
West Indian islands alone furnish 200 species.
The length of the lingual band, and number of rows of teeth borne on it,
vary greatly in different species. But it is among the Pulmonifera we meet
with the most astonishing instances of large numbers of teeth. Limax
maximus possesses 26,800, distributed through 180 rows of 160 each, the
individual teeth measuring only one 10,000th of an inch. Helix pomatia has
21,000, and its comparatively dwarfed congener, H. absoluta, no less than
15,000.
Structure of the Shell of Mollusca.—In my opening sketch of the sub-order
Mollusca an idea may have been gathered of the general character of the
shell covering of these animals. The simplest form of shell occurs in the
rudimentary oval plate of the common slug, Limax rufus. It is embedded in
the shield situated at the back, near the head of the animal. In the Chitons, a
small but singular group of molluscs allied to the univalve limpets, we have
an ovoid shell, made up of eight segments, or movable plates, which give
them a resemblance to enormous woodlice. These have been regarded as
forming a transition series—a link between one division and the other. The
shell in by far the greater portion of all the molluscs is developed from cells
that in process of growth have become hardened by the deposition of
calcareous matter in the interior. This earthy matter consists principally of
calcium carbonate deposited in a crystalline state; and in certain shells, as in
that of the oyster (Plate XVIII., Fig. 8), from the animal cell not having
sufficiently controlled the mode of deposition of the earth particles, they
have assumed the form of perfect rhomboidal crystals.72
PLATE XVIII.
West Indian islands alone furnish 200 species.
The length of the lingual band, and number of rows of teeth borne on it,
vary greatly in different species. But it is among the Pulmonifera we meet
with the most astonishing instances of large numbers of teeth. Limax
maximus possesses 26,800, distributed through 180 rows of 160 each, the
individual teeth measuring only one 10,000th of an inch. Helix pomatia has
21,000, and its comparatively dwarfed congener, H. absoluta, no less than
15,000.
Structure of the Shell of Mollusca.—In my opening sketch of the sub-order
Mollusca an idea may have been gathered of the general character of the
shell covering of these animals. The simplest form of shell occurs in the
rudimentary oval plate of the common slug, Limax rufus. It is embedded in
the shield situated at the back, near the head of the animal. In the Chitons, a
small but singular group of molluscs allied to the univalve limpets, we have
an ovoid shell, made up of eight segments, or movable plates, which give
them a resemblance to enormous woodlice. These have been regarded as
forming a transition series—a link between one division and the other. The
shell in by far the greater portion of all the molluscs is developed from cells
that in process of growth have become hardened by the deposition of
calcareous matter in the interior. This earthy matter consists principally of
calcium carbonate deposited in a crystalline state; and in certain shells, as in
that of the oyster (Plate XVIII., Fig. 8), from the animal cell not having
sufficiently controlled the mode of deposition of the earth particles, they
have assumed the form of perfect rhomboidal crystals.72
PLATE XVIII.
Page 648
SECTIONS OF SHELL-STRUCTURE.
The shell of the wing-shells, Pinna ingens (Plate XVIII., No. 7), is
composed of hexagonal cells, filled with partially translucent calcareous
matter, the outer layer of which can be split up into prism-like columns.
Figs. 3 and 6 are horizontal sections of the Haliotis splendens, with stellate
pigment in a portion of the section, and wavy lines, as in the dentine of the
human tooth, and of Terebratulata rubicuna, showing radiating
perforations. Nos. 4 and 5, sections of the shell of a crab, show pigment
granules beneath the articular layer and the general hexagonal structure of
the next layer.
Some difference of opinion has been expressed with regard to the formation
of pearls, but it is now generally understood to be a diseased condition.
Pearls are matured on a nucleus, consisting of the same matter as that from
The shell of the wing-shells, Pinna ingens (Plate XVIII., No. 7), is
composed of hexagonal cells, filled with partially translucent calcareous
matter, the outer layer of which can be split up into prism-like columns.
Figs. 3 and 6 are horizontal sections of the Haliotis splendens, with stellate
pigment in a portion of the section, and wavy lines, as in the dentine of the
human tooth, and of Terebratulata rubicuna, showing radiating
perforations. Nos. 4 and 5, sections of the shell of a crab, show pigment
granules beneath the articular layer and the general hexagonal structure of
the next layer.
Some difference of opinion has been expressed with regard to the formation
of pearls, but it is now generally understood to be a diseased condition.
Pearls are matured on a nucleus, consisting of the same matter as that from
Page 649
which the new layers of shell proceed at the edge of the mussel or oyster.
The finest kinds are formed in the body of the animal, or originate in the
pearly-looking part of the shell. It is from the size, roundness, and brilliancy
of pearls that their value is estimated.
The microscope discloses a difference in the structure of pearls: those
having a prismatic cellular structure have a brown horny nucleus,
surrounded by small imperfectly-formed prismatic cells; there is also a ring
of horny matter, followed by other prisms, and so on, as represented in Fig.
374; and all transverse sections of pearls from oysters show the same
successive rings of growth or deposit.
Fig. 374.
1. A transverse section of a Pearl from Oyster, showing its prismatic structure 2. A
transverse section of another Pearl, showing its central cellular structure, with
outside rings of true pearly matter. (Magnified 50 diameters.)
The finest kinds are formed in the body of the animal, or originate in the
pearly-looking part of the shell. It is from the size, roundness, and brilliancy
of pearls that their value is estimated.
The microscope discloses a difference in the structure of pearls: those
having a prismatic cellular structure have a brown horny nucleus,
surrounded by small imperfectly-formed prismatic cells; there is also a ring
of horny matter, followed by other prisms, and so on, as represented in Fig.
374; and all transverse sections of pearls from oysters show the same
successive rings of growth or deposit.
Fig. 374.
1. A transverse section of a Pearl from Oyster, showing its prismatic structure 2. A
transverse section of another Pearl, showing its central cellular structure, with
outside rings of true pearly matter. (Magnified 50 diameters.)
Page 650
In a segment of a transverse section of a small purple pearl from a species
of Mytilus (Fig. 375), all trace of prismatic structure has disappeared, and
only a series of fine curved or radiating lines is seen. This pearl consists of a
beautiful purple-coloured series of regular laminæ, many of which have a
series of concentric zones, and are of a yellow tint. The most beautiful
sections for microscopic examination are obtained from Scotch pearls.
Preparation of the Teeth and Shell of Mollusca for Microscopical
Examination.—The method of preparing lingual membranes of Mollusca is
as follows: Under a dissecting microscope, and with a large bull’s eye lens,
cut open and expose to view the floor of the mouth; pin back the cut edges
throughout its length, and work out the dental band with knife and forceps.
The band being detached, place it in a watch-glass, and boil in caustic
potash solution for a few minutes. Having by this process freed the tongue
from its integuments, remove it, wash it well, and place it for a short time in
a dilute acid solution, either acetic or hydrochloric. Wash it well and float it
upon a slide; with a fine sable brush open it out flat, and remove whatever
dirt or fibre may be adhering to it. Lastly, place it in weak spirit and water,
and there let it remain for a few days before mounting in formalin. Canada
balsam renders them rather too pellucid, and the finer teeth are thereby lost.
of Mytilus (Fig. 375), all trace of prismatic structure has disappeared, and
only a series of fine curved or radiating lines is seen. This pearl consists of a
beautiful purple-coloured series of regular laminæ, many of which have a
series of concentric zones, and are of a yellow tint. The most beautiful
sections for microscopic examination are obtained from Scotch pearls.
Preparation of the Teeth and Shell of Mollusca for Microscopical
Examination.—The method of preparing lingual membranes of Mollusca is
as follows: Under a dissecting microscope, and with a large bull’s eye lens,
cut open and expose to view the floor of the mouth; pin back the cut edges
throughout its length, and work out the dental band with knife and forceps.
The band being detached, place it in a watch-glass, and boil in caustic
potash solution for a few minutes. Having by this process freed the tongue
from its integuments, remove it, wash it well, and place it for a short time in
a dilute acid solution, either acetic or hydrochloric. Wash it well and float it
upon a slide; with a fine sable brush open it out flat, and remove whatever
dirt or fibre may be adhering to it. Lastly, place it in weak spirit and water,
and there let it remain for a few days before mounting in formalin. Canada
balsam renders them rather too pellucid, and the finer teeth are thereby lost.
Page 651
Fig. 375.
1. Transverse section of a small Pearl from a Mytilus; 2. Horizontal section
magnified 240 diameters to show prismatic structure and transverse striæ.
The preparation of shell structure must be proceeded with with some
amount of care and caution, or the delicate reticulated network membrane
will be destroyed. If any acid solvent be used to remove the calcareous
structure it should be much diluted, so that the action may proceed slowly
rather than hastily. In the young hermit-crab, for example, where the
calcareous and membranous portions of the shell are continuous, and the
calcium carbonate in a relatively small proportion, a strong acid solution
would entirely destroy the specimen. In the case of nacreous shells the
process of cutting and grinding must also be proceeded with with some
amount of caution. The operation should be examined as the process
proceeds, and under polarised light. Sections of shell structure are usually
mounted in Canada balsam. Under the heading Technique much useful
information on this and kindred subjects will be found in the “Journal of the
Royal Microscopical Society.”
Annulosa, Worms, and Entozoa.
The Annulosa of Huxley embraces the lowest grade of articulated animals,
most of which are now grouped with Metazoa, while some writers place
them in a sub-kingdom Vermes. It appears to me then only possible to
describe this heterogeneous group of worm-like animals among those which
resemble each other in certain negative features, but not possessing any of
the distinctive characters of those previously described. There are numerous
species among Entozoa, every one of which is of the highest interest to
mankind in general, and to animal life as a whole. To these I shall devote
some attention, from the wide-spread importance attached to them. They are
characterised by having a soft absorbent body with little or no colour, in
consequence of being excluded from light, living within the bodies of
animals and absorbing their vital juices, thereby inflicting a large amount of
injury and death upon the whole vertebrate kingdom. They bear in this
respect a close analogy to parasitic Fungi in the nature of their destructive
action upon plant life, which I have fully discussed in a previous chapter.
1. Transverse section of a small Pearl from a Mytilus; 2. Horizontal section
magnified 240 diameters to show prismatic structure and transverse striæ.
The preparation of shell structure must be proceeded with with some
amount of care and caution, or the delicate reticulated network membrane
will be destroyed. If any acid solvent be used to remove the calcareous
structure it should be much diluted, so that the action may proceed slowly
rather than hastily. In the young hermit-crab, for example, where the
calcareous and membranous portions of the shell are continuous, and the
calcium carbonate in a relatively small proportion, a strong acid solution
would entirely destroy the specimen. In the case of nacreous shells the
process of cutting and grinding must also be proceeded with with some
amount of caution. The operation should be examined as the process
proceeds, and under polarised light. Sections of shell structure are usually
mounted in Canada balsam. Under the heading Technique much useful
information on this and kindred subjects will be found in the “Journal of the
Royal Microscopical Society.”
Annulosa, Worms, and Entozoa.
The Annulosa of Huxley embraces the lowest grade of articulated animals,
most of which are now grouped with Metazoa, while some writers place
them in a sub-kingdom Vermes. It appears to me then only possible to
describe this heterogeneous group of worm-like animals among those which
resemble each other in certain negative features, but not possessing any of
the distinctive characters of those previously described. There are numerous
species among Entozoa, every one of which is of the highest interest to
mankind in general, and to animal life as a whole. To these I shall devote
some attention, from the wide-spread importance attached to them. They are
characterised by having a soft absorbent body with little or no colour, in
consequence of being excluded from light, living within the bodies of
animals and absorbing their vital juices, thereby inflicting a large amount of
injury and death upon the whole vertebrate kingdom. They bear in this
respect a close analogy to parasitic Fungi in the nature of their destructive
action upon plant life, which I have fully discussed in a previous chapter.
Page 652
The relations which obtain between parasites and their hosts are in all
respects conditioned by their natural history; and without a detailed
knowledge of the organisation, the development, and the mode of life of the
different species, it is impossible to determine the nature and extent of the
pathological conditions to which they give rise, and at the same time find
means of protection against guests in every way so unwelcome.
The nutritive system of the entozoa must be regarded as in the lowest state
of development, yet there are some among them of a higher grade, as will
be seen as we proceed. All are remarkable alike for their vast
productiveness and for their peculiar metamorphoses. For example, the
greater number of the Tænia begin their lives as sexless, encysted larvæ,
and on entering their final abode, segments are successively added, until the
worm has finally reached the adult stage. Again, the tapeworm of the cat
has its origin in the encysted larvæ found in the livers of the mouse and rat.
Another species of entozoa inhabit the stomach of the stickle-back, and
only attain their perfect form in the stomachs of aquatic birds that feed
exclusively on fish. Another infests the mantle of pond-snails, and through
their agency, the embryos pass into the stomach of sheep.
An almost endless number of similar transformations take place in other
genera. The simplest form among internal parasites is the Gregarinæ,
formerly grouped among Protozoa. They consist of a simple limiting
membrane, with a mass of granular matter enclosed and surrounding a
nucleus (Plate III., No. 53). These parasites pass through a crystoid stage in
the body of one of the lower animals, usually the earthworm, Lumbricus
agricola. In the more mature organism an envelope, differentiated from the
protoplasm within, can be made out (No. 54); this affords an indication of
greater differentiation in the subjacent layer of protoplasm. An anterior
portion is in many cases separated by a constriction from the cylindrical or
band-like body (No. 56). Gregarinæ multiply when encysted, and divide
into a multitude of minute pseudo-navicula, so named from their
resemblance in shape to a well-known form of Diatomaceæ. When a young
pseudo-navicule escapes it behaves somewhat like an amœba, and if
perchance it is swallowed by an appropriate host, it develops at once into
the higher stage. The various forms are represented in Plate III., Nos. 53—
61. Miescher, in 1843, described suchlike bodies, taken from the muscles of
respects conditioned by their natural history; and without a detailed
knowledge of the organisation, the development, and the mode of life of the
different species, it is impossible to determine the nature and extent of the
pathological conditions to which they give rise, and at the same time find
means of protection against guests in every way so unwelcome.
The nutritive system of the entozoa must be regarded as in the lowest state
of development, yet there are some among them of a higher grade, as will
be seen as we proceed. All are remarkable alike for their vast
productiveness and for their peculiar metamorphoses. For example, the
greater number of the Tænia begin their lives as sexless, encysted larvæ,
and on entering their final abode, segments are successively added, until the
worm has finally reached the adult stage. Again, the tapeworm of the cat
has its origin in the encysted larvæ found in the livers of the mouse and rat.
Another species of entozoa inhabit the stomach of the stickle-back, and
only attain their perfect form in the stomachs of aquatic birds that feed
exclusively on fish. Another infests the mantle of pond-snails, and through
their agency, the embryos pass into the stomach of sheep.
An almost endless number of similar transformations take place in other
genera. The simplest form among internal parasites is the Gregarinæ,
formerly grouped among Protozoa. They consist of a simple limiting
membrane, with a mass of granular matter enclosed and surrounding a
nucleus (Plate III., No. 53). These parasites pass through a crystoid stage in
the body of one of the lower animals, usually the earthworm, Lumbricus
agricola. In the more mature organism an envelope, differentiated from the
protoplasm within, can be made out (No. 54); this affords an indication of
greater differentiation in the subjacent layer of protoplasm. An anterior
portion is in many cases separated by a constriction from the cylindrical or
band-like body (No. 56). Gregarinæ multiply when encysted, and divide
into a multitude of minute pseudo-navicula, so named from their
resemblance in shape to a well-known form of Diatomaceæ. When a young
pseudo-navicule escapes it behaves somewhat like an amœba, and if
perchance it is swallowed by an appropriate host, it develops at once into
the higher stage. The various forms are represented in Plate III., Nos. 53—
61. Miescher, in 1843, described suchlike bodies, taken from the muscles of
Page 653
a mouse. A good account of specimens obtained from the muscles of a pig
was published by the late Mr. Rainey in the “Philosophical Transactions,”
1857. He regarded them as cestoid entozoa. They have been described
under a variety of names, as worm-nodules, egg-sacs, eggs of the fluke,
young measles, &c. M. Lieberkühn carefully traced the pseudo-naviculæ
after leaving the perivisceral cavity of the earth-worm; he found large
numbers of small corpuscles, exhibiting amœba-like movements, as well as
pseudo-naviculæ, containing granules, formed in an encysted Gregarinæ.
He imagines that these latter bodies burst, and that their contained granules
develop into the amœbiform bodies which subsequently become Gregarinæ.
Professor Ray Lankester made a careful examination of more than a
hundred worms for the purpose of studying these questions, but he
succeeded in arriving at no other conclusion than that certain forms may be
the by-products of encysted Gregarinæ. The G. lumbricus is one of those
forms which are unilocular. The vesicle is not always very distinct, and is
sometimes altogether absent; occasionally it contains no granules,
sometimes several, one of which is generally nucleated. In other of these
cysts a number of nucleated cells may be seen developing from the
enclosed Gregarina, which gradually become fused together and broken up,
until the entire mass is converted into nucleated bodies, often seen in
different stages of development, assuming the form of a double cone, as that
presented by certain species of Diatomaceæ. At length the cyst contains
nothing but pseudo-naviculæ, sometimes enclosing granules; these
gradually disappear, and finally the cyst bursts. Encystation seems to take
place much more rarely among the bilocular forms of Gregarinæ than in the
unilocular species found in the earthworm and other Annelids.73
Dr. J. Leidy published in the “Transactions of the Philadelphia Society,”
1853, the results of his examinations of several new species of Gregarinæ.
He described a double membrane “within the parietal tunic of the posterior
sac, this being transparent, colourless, and marked by a most beautiful set of
exceedingly regular parallel longitudinal lines.”
Professor R. Leuckart is the latest writer on the parasites of animals, and to
him we are indebted for a more systematic account of the whole group, and
their life-history, than to any previous investigator. I can only attempt to
was published by the late Mr. Rainey in the “Philosophical Transactions,”
1857. He regarded them as cestoid entozoa. They have been described
under a variety of names, as worm-nodules, egg-sacs, eggs of the fluke,
young measles, &c. M. Lieberkühn carefully traced the pseudo-naviculæ
after leaving the perivisceral cavity of the earth-worm; he found large
numbers of small corpuscles, exhibiting amœba-like movements, as well as
pseudo-naviculæ, containing granules, formed in an encysted Gregarinæ.
He imagines that these latter bodies burst, and that their contained granules
develop into the amœbiform bodies which subsequently become Gregarinæ.
Professor Ray Lankester made a careful examination of more than a
hundred worms for the purpose of studying these questions, but he
succeeded in arriving at no other conclusion than that certain forms may be
the by-products of encysted Gregarinæ. The G. lumbricus is one of those
forms which are unilocular. The vesicle is not always very distinct, and is
sometimes altogether absent; occasionally it contains no granules,
sometimes several, one of which is generally nucleated. In other of these
cysts a number of nucleated cells may be seen developing from the
enclosed Gregarina, which gradually become fused together and broken up,
until the entire mass is converted into nucleated bodies, often seen in
different stages of development, assuming the form of a double cone, as that
presented by certain species of Diatomaceæ. At length the cyst contains
nothing but pseudo-naviculæ, sometimes enclosing granules; these
gradually disappear, and finally the cyst bursts. Encystation seems to take
place much more rarely among the bilocular forms of Gregarinæ than in the
unilocular species found in the earthworm and other Annelids.73
Dr. J. Leidy published in the “Transactions of the Philadelphia Society,”
1853, the results of his examinations of several new species of Gregarinæ.
He described a double membrane “within the parietal tunic of the posterior
sac, this being transparent, colourless, and marked by a most beautiful set of
exceedingly regular parallel longitudinal lines.”
Professor R. Leuckart is the latest writer on the parasites of animals, and to
him we are indebted for a more systematic account of the whole group, and
their life-history, than to any previous investigator. I can only attempt to
Page 654
give a mere outline of the developmental stages of a few typical forms of
parasites, commencing with the cystic tapeworm, Tænia. These worms are
ribbon-like in appearance, and are divided throughout the greater part of
their length into segments, and their usual habitation is the intestinal cavity
of vertebrate animals. The anterior extremity of a tænoid worm is usually
called the head, and bears the organ by which the animal attaches itself to
the mucous membrane of the creature which it infests. These organs are
either suckers, or hooks, or both conjoined. In Tænia, four suckers are
combined with a circlet of hooks, disposed around a median terminal
prominence. The embryo passes through certain stages of development—
viz., four forms or changes: but the embryo itself is very peculiar,
consisting of an oval non-ciliated mass, provided with six hooks, three upon
each side of the middle line. Tænia are found enclosed in various situations
besides that of the alimentary canal: the eye, the brain, the muscular tissues,
the liver, &c., of animals. The following cystic worms are usually included
in this genera, Cysticercus Anthocephalus, Cœnurus, and T. Echinococcus.
Plate IV., No. 100, shows an adult specimen of the latter with rostellum
suckers, and three successive segments, the last of which is the ova sac. The
water-vascular system is represented coloured by carmine. This parasite
infests the human body as frequently as many other species. My accurately-
drawn figure is copied from Cobbold’s “Introduction to the Study of
Entozoa.”
Cysticercus fasciolaris is developed within the liver of white mice;
Cysticercus cellulosæ in the muscles of the pig; hence we have the diseased
state of pork familiarly known as “measly pork.” Should a lamb become
infested with Tænia the final transformation will be different; within a
fortnight symptoms of a disease known as “staggers” manifest themselves,
and in the course of a few weeks the Cœnurus cerebralis will be developed
within the brain. Von Siebold pointed out the bearing of this fact upon the
important practical problem of the prevention of “staggers.” Others
belonging to the same class of parasites are quite as remarkable in their
preference for the alimentary canal of fishes. The Echinorhynchus is
developed in the intestinal canal of the flounder, Triænophorus nodulus in
the liver of the salmon. Thus, by careful and repeated observation with the
microscope, a close connection is found to exist between the cystic and
cestoid entozoa.
parasites, commencing with the cystic tapeworm, Tænia. These worms are
ribbon-like in appearance, and are divided throughout the greater part of
their length into segments, and their usual habitation is the intestinal cavity
of vertebrate animals. The anterior extremity of a tænoid worm is usually
called the head, and bears the organ by which the animal attaches itself to
the mucous membrane of the creature which it infests. These organs are
either suckers, or hooks, or both conjoined. In Tænia, four suckers are
combined with a circlet of hooks, disposed around a median terminal
prominence. The embryo passes through certain stages of development—
viz., four forms or changes: but the embryo itself is very peculiar,
consisting of an oval non-ciliated mass, provided with six hooks, three upon
each side of the middle line. Tænia are found enclosed in various situations
besides that of the alimentary canal: the eye, the brain, the muscular tissues,
the liver, &c., of animals. The following cystic worms are usually included
in this genera, Cysticercus Anthocephalus, Cœnurus, and T. Echinococcus.
Plate IV., No. 100, shows an adult specimen of the latter with rostellum
suckers, and three successive segments, the last of which is the ova sac. The
water-vascular system is represented coloured by carmine. This parasite
infests the human body as frequently as many other species. My accurately-
drawn figure is copied from Cobbold’s “Introduction to the Study of
Entozoa.”
Cysticercus fasciolaris is developed within the liver of white mice;
Cysticercus cellulosæ in the muscles of the pig; hence we have the diseased
state of pork familiarly known as “measly pork.” Should a lamb become
infested with Tænia the final transformation will be different; within a
fortnight symptoms of a disease known as “staggers” manifest themselves,
and in the course of a few weeks the Cœnurus cerebralis will be developed
within the brain. Von Siebold pointed out the bearing of this fact upon the
important practical problem of the prevention of “staggers.” Others
belonging to the same class of parasites are quite as remarkable in their
preference for the alimentary canal of fishes. The Echinorhynchus is
developed in the intestinal canal of the flounder, Triænophorus nodulus in
the liver of the salmon. Thus, by careful and repeated observation with the
microscope, a close connection is found to exist between the cystic and
cestoid entozoa.
Page 655
The Echinococcus (Plate IV., No. 101) infests the human liver. These
parasites are always found in cysts, and in closed cavities in the interior of
the body. They are united in fours by a very short stalk or pedicle, common
to the whole. By an increase of magnification the contents of a cyst present
the several structures represented in Fig. 376.
Echinorhynchus, or spiny-headed threadworms, constitute a group of
entozoa which undergo a metamorphosis hardly, perhaps, less remarkable
than that known to take place in other Nematode worms. Leuckart
instituted, in 1861, a series of experiments with the ova of Echinorhynchus
proteus found parasitic upon the Gammarus pulex. The ova of E. proteus
resemble in form and structure those of allied species. They are of a
fusiform shape, surrounded with two membranes, an external of a more
albuminous nature, and an internal chitinous one. When the eggs reach the
intestine the outer of these membranes is absent, being in fact digested,
while the inner remains intact until ruptured by the embryo.
parasites are always found in cysts, and in closed cavities in the interior of
the body. They are united in fours by a very short stalk or pedicle, common
to the whole. By an increase of magnification the contents of a cyst present
the several structures represented in Fig. 376.
Echinorhynchus, or spiny-headed threadworms, constitute a group of
entozoa which undergo a metamorphosis hardly, perhaps, less remarkable
than that known to take place in other Nematode worms. Leuckart
instituted, in 1861, a series of experiments with the ova of Echinorhynchus
proteus found parasitic upon the Gammarus pulex. The ova of E. proteus
resemble in form and structure those of allied species. They are of a
fusiform shape, surrounded with two membranes, an external of a more
albuminous nature, and an internal chitinous one. When the eggs reach the
intestine the outer of these membranes is absent, being in fact digested,
while the inner remains intact until ruptured by the embryo.
Page 656
Fig. 376.—Cystic Disease of Liver (Human).
a. Cyst with Echinococcus enclosed; b. detached hooklets from the head of
Echinococcus, magnified 250 diameters; c. crystals found in cyst, chiefly
cholesterine; d. cylindrical epithelium, some enclosed in structureless vesicles; e.
Puro-muculent granules, fat and blood corpuscles.
The typical Threadworm belonging to the order Nematoidea infest the
intestines of children, and are a source of much suffering. The egg is
elliptical, and contains a mass of granular protoplasm, the external wall of
which soon becomes marked out into a layer of cells. The mouth of the
worm appears as a depression at the end of the blunt head. When the
muscular system and alimentary canal are developed the embryo hatches
out, some few of which are free living forms; most of them lead a parasitic
life. Their reproduction is enormous, representing thousands of eggs and
embryos.
Of the non-parasitic species of thread-worm, the common vinegar eel,
Anguillula,74 affords an example. This is found in polluted water, bog-moss,
and moist earth, as well as in vinegar; also in the alimentary canal of the
pond-snail, the frog, fish, &c. Another species is met with in the ears of
wheat affected with a blight termed the “cockle”; another, the A. glutinis, in
sour paste. If grains of the affected wheat are soaked in water for an hour or
two before they are cut open, the so called “eels” will be found. The paste-
eel makes its appearance spontaneously just as the pasty mass is turning
sour; the means of securing a supply for microscopical examination consists
in allowing a portion of the paste in which they show themselves to dry up,
and laying it by for stock; if at any time a portion of this is introduced into a
a. Cyst with Echinococcus enclosed; b. detached hooklets from the head of
Echinococcus, magnified 250 diameters; c. crystals found in cyst, chiefly
cholesterine; d. cylindrical epithelium, some enclosed in structureless vesicles; e.
Puro-muculent granules, fat and blood corpuscles.
The typical Threadworm belonging to the order Nematoidea infest the
intestines of children, and are a source of much suffering. The egg is
elliptical, and contains a mass of granular protoplasm, the external wall of
which soon becomes marked out into a layer of cells. The mouth of the
worm appears as a depression at the end of the blunt head. When the
muscular system and alimentary canal are developed the embryo hatches
out, some few of which are free living forms; most of them lead a parasitic
life. Their reproduction is enormous, representing thousands of eggs and
embryos.
Of the non-parasitic species of thread-worm, the common vinegar eel,
Anguillula,74 affords an example. This is found in polluted water, bog-moss,
and moist earth, as well as in vinegar; also in the alimentary canal of the
pond-snail, the frog, fish, &c. Another species is met with in the ears of
wheat affected with a blight termed the “cockle”; another, the A. glutinis, in
sour paste. If grains of the affected wheat are soaked in water for an hour or
two before they are cut open, the so called “eels” will be found. The paste-
eel makes its appearance spontaneously just as the pasty mass is turning
sour; the means of securing a supply for microscopical examination consists
in allowing a portion of the paste in which they show themselves to dry up,
and laying it by for stock; if at any time a portion of this is introduced into a
Page 657
little fresh-made paste, and the whole kept warm and moist for a few hours,
it will be found to swarm with these wriggling little worms. A small portion
of paste spread over the face of a Coddington lens is a ready way of
viewing them.
Trichina spiralis.—One of the smallest and most dangerous of all human
internal parasites is T. spiralis, since it finds its way into the muscles
throughout the human body. The young animal presents the form of a
spirally-coiled worm in the interior of a minute oval-shaped cyst (Plate IV.,
No. 104), a mere speck scarcely visible to the naked eye. In the muscular
structure it resembles a small millet seed, somewhat calcareous in
composition. The history of the development of Trichina in the human
muscle is briefly that in a few hours after the ingestion of infected pork,
Trichina, disengaged from the muscle, will be found in the stomach: hence
they pass into the small intestine, where they are further developed.
Continuing their migrations, they penetrate far into the interior of the
primitive muscular fasciculi, where they will be found, in about three days
after ingestion, in considerable numbers, and so far developed that the
young entozoa have almost attained a size equal to that of the full-grown
Trichina (Plate IV., No. 105). They quickly advance into the interior of the
muscular fasciculi, where they live and multiply in continuous series, while
the surrounding structures as well as the muscular tissue undergo a process
of histolysis. The destructive nature of the parasite is very great.
The number of progeny produced by one female may amount to several
thousands, and as soon as they leave the egg they either penetrate through
the blood-vessels, or are carried on by the circulation, and ultimately
become lodged in the muscles situated in the most distant parts of the body.
Here, as already explained, they become encysted.
it will be found to swarm with these wriggling little worms. A small portion
of paste spread over the face of a Coddington lens is a ready way of
viewing them.
Trichina spiralis.—One of the smallest and most dangerous of all human
internal parasites is T. spiralis, since it finds its way into the muscles
throughout the human body. The young animal presents the form of a
spirally-coiled worm in the interior of a minute oval-shaped cyst (Plate IV.,
No. 104), a mere speck scarcely visible to the naked eye. In the muscular
structure it resembles a small millet seed, somewhat calcareous in
composition. The history of the development of Trichina in the human
muscle is briefly that in a few hours after the ingestion of infected pork,
Trichina, disengaged from the muscle, will be found in the stomach: hence
they pass into the small intestine, where they are further developed.
Continuing their migrations, they penetrate far into the interior of the
primitive muscular fasciculi, where they will be found, in about three days
after ingestion, in considerable numbers, and so far developed that the
young entozoa have almost attained a size equal to that of the full-grown
Trichina (Plate IV., No. 105). They quickly advance into the interior of the
muscular fasciculi, where they live and multiply in continuous series, while
the surrounding structures as well as the muscular tissue undergo a process
of histolysis. The destructive nature of the parasite is very great.
The number of progeny produced by one female may amount to several
thousands, and as soon as they leave the egg they either penetrate through
the blood-vessels, or are carried on by the circulation, and ultimately
become lodged in the muscles situated in the most distant parts of the body.
Here, as already explained, they become encysted.
Page 658
Fig. 377.—Monads in Rat’s Blood, stained with methyl violet, showing membrane
under different aspects; blood-corpuscles, some crenated and others with stained
discs (× 1,200).—(Crookshank.)
Professor Virchow draws the following conclusions:—“1. The ingestion of
pig’s flesh, fresh or badly dressed, containing Trichinæ, is attended with the
greatest danger, and may prove the proximate cause of death. 2. The
Trichinæ maintain their living properties in decomposed flesh; they resist
immersion in water for weeks together, and when encysted may, without
injury to their vitality, be plunged in a sufficiently dilute solution of
chromic acid for at least ten days. 3. On the contrary, they perish and are
deprived of all noxious influence in ham which has been well smoked, kept
a sufficient length of time, and then well boiled before it is consumed.”
A more minute Filarian worm has been detected in the human blood-
vessels, known as Filaria sanguinis hominis. This worm carries on its work
of destruction throughout the night; during the day it remains perfectly
passive. It increases rapidly, and produces swellings of the glandular
structures of the body, somewhat after the nature of those characteristic of
the Bombay plague, with a slight difference, that after death the swellings
are seen to be due to the vast accumulations of the Filaria sanguinis
blocking the blood-vessels. The accompanying Fig. 377 shows a similar
infiltration of monads in the blood of rats dying of plague in Bombay.
Trematode Worms.—In the order Trematoda, to which the fluke belongs, the
body is unsegmented, and to the naked eye smooth throughout, with a blood
circulatory system, and two suctorial discs at the hinder end. There is a
under different aspects; blood-corpuscles, some crenated and others with stained
discs (× 1,200).—(Crookshank.)
Professor Virchow draws the following conclusions:—“1. The ingestion of
pig’s flesh, fresh or badly dressed, containing Trichinæ, is attended with the
greatest danger, and may prove the proximate cause of death. 2. The
Trichinæ maintain their living properties in decomposed flesh; they resist
immersion in water for weeks together, and when encysted may, without
injury to their vitality, be plunged in a sufficiently dilute solution of
chromic acid for at least ten days. 3. On the contrary, they perish and are
deprived of all noxious influence in ham which has been well smoked, kept
a sufficient length of time, and then well boiled before it is consumed.”
A more minute Filarian worm has been detected in the human blood-
vessels, known as Filaria sanguinis hominis. This worm carries on its work
of destruction throughout the night; during the day it remains perfectly
passive. It increases rapidly, and produces swellings of the glandular
structures of the body, somewhat after the nature of those characteristic of
the Bombay plague, with a slight difference, that after death the swellings
are seen to be due to the vast accumulations of the Filaria sanguinis
blocking the blood-vessels. The accompanying Fig. 377 shows a similar
infiltration of monads in the blood of rats dying of plague in Bombay.
Trematode Worms.—In the order Trematoda, to which the fluke belongs, the
body is unsegmented, and to the naked eye smooth throughout, with a blood
circulatory system, and two suctorial discs at the hinder end. There is a
Page 659
distinct digestive canal, usually forked, furnished with only one aperture,
the mouth. The excretory organs open out as in tape worms, and the male
and female organs co-exist in the same individual.
The Fluke (shown in Plate IV., No. 103) is cone-shaped, and is the
Amphistome conicum of Rudolphi. This parasite is common in oxen, sheep,
and deer, and it has also been found in the Dorcas antelope. It invariably
takes up its abode in the first stomach, or rumen, attaching itself to the
papillated folds of the mucous membrane. In the full-grown, adult stage, it
rarely exceeds half an inch in length. It is certainly one of the most
remarkable in form and organisation of any of the internal parasites.
The larger fluke (Fasciola hepatica) often attains to an inch or more in size.
It is not only of frequent occurrence in all varieties of grazing cattle, but has
likewise been found in the horse, the ass, and also in the hare and rabbit and
other animals. Its occurrence in man has been recorded by more than one
observer. The oral sucker forming the mouth leads to a short œsophagus,
which very soon divides into two primary stomachal or intestinal trunks, the
latter in their turn sending off branches; the whole together forming that
attractive dendritic system of vessels so often compared to plant-venation.
This remarkably-formed digestive apparatus is represented in Plate IV.,
Nos. 106 and 107, Fasciola gigantea of Cobbold, and should be contrasted
with the somewhat similarly racemose character of the water-vascular
system. Let it be expressly noted, however, that in the digestive system the
majority of the tubes branch out in a direction obliquely downwards,
whereas those of the vascular system slope obliquely upwards. A further
comparison of the disposition of these two systems of structure, with the
same systems figured and described as characteristic of the Amphistoma,
will at once serve to demonstrate the important differences which subsist
between the several members of the two genera, if we turn to the
consideration of the habits of Fasciola hepatica, which, in so far as they
relate to excitation of the liver disease in sheep, acquire the highest practical
importance. Intelligent cattle-breeders, agriculturists, and veterinarians have
all along observed that the rot, as this disease is commonly called, is
particularly prevalent after long-continued wet weather, and more especially
so if there have been a succession of wet seasons; and from this
circumstance they have very naturally inferred that the humidity of the
the mouth. The excretory organs open out as in tape worms, and the male
and female organs co-exist in the same individual.
The Fluke (shown in Plate IV., No. 103) is cone-shaped, and is the
Amphistome conicum of Rudolphi. This parasite is common in oxen, sheep,
and deer, and it has also been found in the Dorcas antelope. It invariably
takes up its abode in the first stomach, or rumen, attaching itself to the
papillated folds of the mucous membrane. In the full-grown, adult stage, it
rarely exceeds half an inch in length. It is certainly one of the most
remarkable in form and organisation of any of the internal parasites.
The larger fluke (Fasciola hepatica) often attains to an inch or more in size.
It is not only of frequent occurrence in all varieties of grazing cattle, but has
likewise been found in the horse, the ass, and also in the hare and rabbit and
other animals. Its occurrence in man has been recorded by more than one
observer. The oral sucker forming the mouth leads to a short œsophagus,
which very soon divides into two primary stomachal or intestinal trunks, the
latter in their turn sending off branches; the whole together forming that
attractive dendritic system of vessels so often compared to plant-venation.
This remarkably-formed digestive apparatus is represented in Plate IV.,
Nos. 106 and 107, Fasciola gigantea of Cobbold, and should be contrasted
with the somewhat similarly racemose character of the water-vascular
system. Let it be expressly noted, however, that in the digestive system the
majority of the tubes branch out in a direction obliquely downwards,
whereas those of the vascular system slope obliquely upwards. A further
comparison of the disposition of these two systems of structure, with the
same systems figured and described as characteristic of the Amphistoma,
will at once serve to demonstrate the important differences which subsist
between the several members of the two genera, if we turn to the
consideration of the habits of Fasciola hepatica, which, in so far as they
relate to excitation of the liver disease in sheep, acquire the highest practical
importance. Intelligent cattle-breeders, agriculturists, and veterinarians have
all along observed that the rot, as this disease is commonly called, is
particularly prevalent after long-continued wet weather, and more especially
so if there have been a succession of wet seasons; and from this
circumstance they have very naturally inferred that the humidity of the
Page 660
atmosphere, coupled with a moist condition of the soil, forms the sole cause
of the malady. Co-ordinating with these facts, it has likewise been noticed
that the flocks grazing in low pastures and marshy districts are much more
liable to the invasion of this endemic disease than are those pasturing on
higher and drier grounds; a noteworthy exception occurring in the case of
those flocks feeding in the salt-water marshes on our eastern shores. Plate
IV., No. 106, Fasciola gigantea: the anterior surface is exposed to display
oral and ventral suckers, and the dendriform digestive apparatus injected
with ultra-marine; No. 107 shows the dorsal aspect of the specimen and the
multiramose character of the water-vascular system, the vessels being
injected with vermilion.
In their larval condition the Amphistoma live in or upon the body of the
pond-snail. This we infer from the circumstance that the larvæ, or cercariæ,
of a closely-allied species, the Amphistoma subclavatum, are known to
infest the alimentary canal of frogs and newts, and have also been found on
the body of the Planorbis by myself. The cercariæ larvæ are taken, it is
believed, by the sheep and the cattle while drinking. The earliest embryotic
stage in which I have found the embryo fluke is represented at Fig. 378, No.
1. In the year 1854, whilst observing the habits of Limnœa and other water-
snails, I brought home specimens from the ornamental water in the Botanic
Gardens; upon these were discovered thousands of minute thread-like
worms, subsequently met with on other embryos, and at first taken to be
simple infusorial animals, but upon placing them in a glass vessel these
minute bodies were observed to detach themselves and commence a free-
swimming existence. A fringe of cilia was seen to surround the flask-shaped
body (No. 1).
of the malady. Co-ordinating with these facts, it has likewise been noticed
that the flocks grazing in low pastures and marshy districts are much more
liable to the invasion of this endemic disease than are those pasturing on
higher and drier grounds; a noteworthy exception occurring in the case of
those flocks feeding in the salt-water marshes on our eastern shores. Plate
IV., No. 106, Fasciola gigantea: the anterior surface is exposed to display
oral and ventral suckers, and the dendriform digestive apparatus injected
with ultra-marine; No. 107 shows the dorsal aspect of the specimen and the
multiramose character of the water-vascular system, the vessels being
injected with vermilion.
In their larval condition the Amphistoma live in or upon the body of the
pond-snail. This we infer from the circumstance that the larvæ, or cercariæ,
of a closely-allied species, the Amphistoma subclavatum, are known to
infest the alimentary canal of frogs and newts, and have also been found on
the body of the Planorbis by myself. The cercariæ larvæ are taken, it is
believed, by the sheep and the cattle while drinking. The earliest embryotic
stage in which I have found the embryo fluke is represented at Fig. 378, No.
1. In the year 1854, whilst observing the habits of Limnœa and other water-
snails, I brought home specimens from the ornamental water in the Botanic
Gardens; upon these were discovered thousands of minute thread-like
worms, subsequently met with on other embryos, and at first taken to be
simple infusorial animals, but upon placing them in a glass vessel these
minute bodies were observed to detach themselves and commence a free-
swimming existence. A fringe of cilia was seen to surround the flask-shaped
body (No. 1).
Page 661
Fig. 378.—Forms of Cercaria; stages in the development of the Fluke.
1. An infusorial embryo; 2. a Trematode embryo having quite recently escaped
from the egg; 3. embryo cercaria; 4. fully-formed cercaria, showing alimentary
canal and sucker-like head; 5. encysted form of same; 6. Cercaria furcata, with the
nervous system and forked tail displayed; 7. in the act of breaking up; 8. tail
portion half an hour after division; 9. parasitic worm of another species of
Trematoda. (Magnified from 10 to 25 diameters.)
The study of these embryos throws a flood of light upon the obscure history
of Cercariæ. After a short period of wandering, their embryos fasten upon
the water-snail, and compel it to act as a wet-nurse, and prepare it for a
further and higher stage of life. The earliest condition in which I have
discovered them concealed about the body of the water-snail is shown at
No. 2; in appearance, a simple elongated sac filled with ova or germs, and
which in a short time develop into the caudate worms already spoken of;
1. An infusorial embryo; 2. a Trematode embryo having quite recently escaped
from the egg; 3. embryo cercaria; 4. fully-formed cercaria, showing alimentary
canal and sucker-like head; 5. encysted form of same; 6. Cercaria furcata, with the
nervous system and forked tail displayed; 7. in the act of breaking up; 8. tail
portion half an hour after division; 9. parasitic worm of another species of
Trematoda. (Magnified from 10 to 25 diameters.)
The study of these embryos throws a flood of light upon the obscure history
of Cercariæ. After a short period of wandering, their embryos fasten upon
the water-snail, and compel it to act as a wet-nurse, and prepare it for a
further and higher stage of life. The earliest condition in which I have
discovered them concealed about the body of the water-snail is shown at
No. 2; in appearance, a simple elongated sac filled with ova or germs, and
which in a short time develop into the caudate worms already spoken of;
Page 662
their tails gradually attaining to the length of the mature embryos, Nos. 3
and 4, the latter being a full-grown Cercaria ephemera.
Diesing described no less than twelve species of Cercariæ, some of the most
curious of which live on the puddle-snail, in colonies of thousands. All
throw off their tails at the moment of changing into a fluke. On placing
some Cercaria furcata (Nos. 6 and 7) under the microscope, they were seen
to plunge about in frantic attempts to escape from confinement. Suddenly I
saw them shed their tails and their bodies divide into two parts, each half
swimming about as vigorously as before, quite indifferent as to the
severance, and apparently dying from exhaustion. Those represented in
Nos. 6 and 7 have a highly-organised nervous system, forming a continuous
circuit throughout the body and tail. The mouth is furnished with a sucker
and hooklets, which can be projected out some distance, while a digestive
apparatus and ventral opening or sucker can be differentiated. The tail is
bifurcated and articulated with the body by a sort of ball-and-socket joint,
and when broken off, the convexity of one part is seen to accurately fit into
the concavity of the other; it lashes about this appendage with considerable
dexterity, rarely attaching itself to any of the small aquatic plants.75
There is yet another Filarian worm, a pest to the poultry-yard, the Gape-
worm, Sclerostoma syngamus. This parasite is widely distributed, and is
invested with special interest, since it produces disease, and kills annually
thousands of young chickens, pheasants, partridges, and many of the larger
kinds of wild birds. The worms find their way into the windpipe or tracheæ,
through the drinking water, while in the embryotic or cercarian stage of
existence, and their increase is so rapid, the birds quickly die of suffocation.
The female gape-worm often attains to a considerable size, and when full
grown resembles the well-known mud-worm of the Thames (Gordius
aquaticus). She measures full six-eighths of an inch in length, while the
male only measures one-eighth. So insignificantly small is he that the
female carries him about tucked into a side pocket. The ova sac occupies a
considerable portion of the internal body space, and is always found loaded
with eggs in all stages of development, numbering some five hundred or a
thousand. In shape these are ovoid. On cutting open the windpipe of
chicken and partridges, I have found their tracheæ literally swarming with
the gape-worm.76
and 4, the latter being a full-grown Cercaria ephemera.
Diesing described no less than twelve species of Cercariæ, some of the most
curious of which live on the puddle-snail, in colonies of thousands. All
throw off their tails at the moment of changing into a fluke. On placing
some Cercaria furcata (Nos. 6 and 7) under the microscope, they were seen
to plunge about in frantic attempts to escape from confinement. Suddenly I
saw them shed their tails and their bodies divide into two parts, each half
swimming about as vigorously as before, quite indifferent as to the
severance, and apparently dying from exhaustion. Those represented in
Nos. 6 and 7 have a highly-organised nervous system, forming a continuous
circuit throughout the body and tail. The mouth is furnished with a sucker
and hooklets, which can be projected out some distance, while a digestive
apparatus and ventral opening or sucker can be differentiated. The tail is
bifurcated and articulated with the body by a sort of ball-and-socket joint,
and when broken off, the convexity of one part is seen to accurately fit into
the concavity of the other; it lashes about this appendage with considerable
dexterity, rarely attaching itself to any of the small aquatic plants.75
There is yet another Filarian worm, a pest to the poultry-yard, the Gape-
worm, Sclerostoma syngamus. This parasite is widely distributed, and is
invested with special interest, since it produces disease, and kills annually
thousands of young chickens, pheasants, partridges, and many of the larger
kinds of wild birds. The worms find their way into the windpipe or tracheæ,
through the drinking water, while in the embryotic or cercarian stage of
existence, and their increase is so rapid, the birds quickly die of suffocation.
The female gape-worm often attains to a considerable size, and when full
grown resembles the well-known mud-worm of the Thames (Gordius
aquaticus). She measures full six-eighths of an inch in length, while the
male only measures one-eighth. So insignificantly small is he that the
female carries him about tucked into a side pocket. The ova sac occupies a
considerable portion of the internal body space, and is always found loaded
with eggs in all stages of development, numbering some five hundred or a
thousand. In shape these are ovoid. On cutting open the windpipe of
chicken and partridges, I have found their tracheæ literally swarming with
the gape-worm.76
Page 663
A remarkable form of the Trematode worm is Bilharzia hæmatobra of
Cobbold, Distomia hæmatobium of other authors (Plate IV., No. 102). This
genus of fluke, discovered by Dr. Bilharz in the human portal system of
blood vessels, gives rise to a very serious state of disease among the
Egyptians. So common is the occurrence of this worm, that this physician
expressed his belief that half the grown-up population of Egypt suffer from
it. Griesinger conjectures that the young of the parasite exist in the waters
of the Nile, and in the fish which abound. Dr. Cobbold thinks “it more
probable that the larvæ, in the form of cercariæ, rediæ, and sporocysts, will
be found in certain gasteropod mollusca proper to the locality.” The
anatomy of this fluke is fully described by Küchenmeister in his book on
parasites, by Leuckart,77 and by Cobbold. The eggs and embryos of
Bilharzia are peculiar in possessing the power of altering their forms in both
stages of life; and it is more than probable that the embryo form has been
mistaken for some extraordinary form of ciliated infusorial animal, its
movements being quick and lively. We cannot fail to notice the curious
form of the male animal, and, unlike the Filarian previously described, it is
he who carries the female about and feeds her. The whip-like appendage
seen in the figure is a portion of the body of the female. The disease
produced by this parasite is said to be more virulent in the summer months,
probably owing to the greater abundance of cercarian larvæ at this period of
the year.
Cobbold, Distomia hæmatobium of other authors (Plate IV., No. 102). This
genus of fluke, discovered by Dr. Bilharz in the human portal system of
blood vessels, gives rise to a very serious state of disease among the
Egyptians. So common is the occurrence of this worm, that this physician
expressed his belief that half the grown-up population of Egypt suffer from
it. Griesinger conjectures that the young of the parasite exist in the waters
of the Nile, and in the fish which abound. Dr. Cobbold thinks “it more
probable that the larvæ, in the form of cercariæ, rediæ, and sporocysts, will
be found in certain gasteropod mollusca proper to the locality.” The
anatomy of this fluke is fully described by Küchenmeister in his book on
parasites, by Leuckart,77 and by Cobbold. The eggs and embryos of
Bilharzia are peculiar in possessing the power of altering their forms in both
stages of life; and it is more than probable that the embryo form has been
mistaken for some extraordinary form of ciliated infusorial animal, its
movements being quick and lively. We cannot fail to notice the curious
form of the male animal, and, unlike the Filarian previously described, it is
he who carries the female about and feeds her. The whip-like appendage
seen in the figure is a portion of the body of the female. The disease
produced by this parasite is said to be more virulent in the summer months,
probably owing to the greater abundance of cercarian larvæ at this period of
the year.
Page 664
Fig. 379.—The double parasitic worm (Diplozoum paradoxum).
There are also double parasitic worms, which may be described as a sub-
order of Trematoda, differing very much from those previously described.
These live on the gills of several species of fresh-water fish, the gudgeon
and minnow, for instance. Among them is a most remarkable creature well
deserving the name of Diplozoum paradoxum which has been bestowed
upon it. It consists of two complete mature similar halves, each possessing
every attribute of a perfect animal (a). Each of the pointed front ends has a
mouth aperture, and close to it two small sucking discs; while each
individual has a separate intestine, consisting of a medium tube and
innumerable side-branches. At the hinder end of the body are two suckers
sunk in a depression, and protected by four hard buckle-shaped organs. The
eggs are elongated, and provided at one end with a fine thread-like
There are also double parasitic worms, which may be described as a sub-
order of Trematoda, differing very much from those previously described.
These live on the gills of several species of fresh-water fish, the gudgeon
and minnow, for instance. Among them is a most remarkable creature well
deserving the name of Diplozoum paradoxum which has been bestowed
upon it. It consists of two complete mature similar halves, each possessing
every attribute of a perfect animal (a). Each of the pointed front ends has a
mouth aperture, and close to it two small sucking discs; while each
individual has a separate intestine, consisting of a medium tube and
innumerable side-branches. At the hinder end of the body are two suckers
sunk in a depression, and protected by four hard buckle-shaped organs. The
eggs are elongated, and provided at one end with a fine thread-like
Page 665
appendage (b). In this egg the young (c)—which at the time of hatching is
only about one-hundredth of an inch—takes about a fortnight to develop. It
is covered with cilia, has two eyes and two suckers; after quitting the egg,
the larvæ are very lively and restless in their movements, gliding about and
then swimming off with rapidity. If unable to find the fish into which they
are destined to live, they grow feeble and perish, but if successful they grow
into the Diporpa (d), which is flattened and lancet-shaped, and bears a small
sucking disc on the under surface and a conical excrescence on the back.
After living in this state for some weeks, and gaining nourishment by
sucking the blood from the fish’s gills, the worms begin to join together in
pairs, one specimen seizing the conical excrescence of another by its
ventrical sucker; then, by a truly acrobatic feat, the second twists itself to
the dorsal excrescence of the first, and in this state an inseparable fusion
takes place between the suckers and the excrescences involved in the
adhesion.78
In the group Vermes, the more highly-organised Annelida must be included.
These, for the most part, live either in fresh or salt water. The Annelids are
various, while the Planaria, a genus of Turbellaria, are very common in
pools, and resemble minute leeches; their motion is continuous and gliding,
and they are always found crawling over the surfaces of aquatic plants and
animals, both in fresh and salt water. The body has the flattened sole-like
shape of the Trematode entozoa (Fig. 378, No. 9), the mouth is surrounded
by a circular sucker; this is applied to the surface of the plant from which
the animal draws its nourishment; it is also furnished with a rather long
proboscis, which is probably employed for a similar purpose.
Planariæ multiply by eggs, and by spontaneous fissuration in a transverse
direction, each segment becoming a perfect animal. Professor Agassiz
believes that the infusorial animals, Paramæcium and Kolpoda, are simply
planarian larvæ.
Hirudinidæ, the leech tribe, are usually believed to form a link between the
Annelida on the one hand, and the Trematoda on the other; their affinities
place them closer with the latter than the former. Although deprived of the
characteristic setæ of the Annelida, and exhibiting no sectional divisions,
they are provided with a sucker-like mouth possessed by Trematoda, but
only about one-hundredth of an inch—takes about a fortnight to develop. It
is covered with cilia, has two eyes and two suckers; after quitting the egg,
the larvæ are very lively and restless in their movements, gliding about and
then swimming off with rapidity. If unable to find the fish into which they
are destined to live, they grow feeble and perish, but if successful they grow
into the Diporpa (d), which is flattened and lancet-shaped, and bears a small
sucking disc on the under surface and a conical excrescence on the back.
After living in this state for some weeks, and gaining nourishment by
sucking the blood from the fish’s gills, the worms begin to join together in
pairs, one specimen seizing the conical excrescence of another by its
ventrical sucker; then, by a truly acrobatic feat, the second twists itself to
the dorsal excrescence of the first, and in this state an inseparable fusion
takes place between the suckers and the excrescences involved in the
adhesion.78
In the group Vermes, the more highly-organised Annelida must be included.
These, for the most part, live either in fresh or salt water. The Annelids are
various, while the Planaria, a genus of Turbellaria, are very common in
pools, and resemble minute leeches; their motion is continuous and gliding,
and they are always found crawling over the surfaces of aquatic plants and
animals, both in fresh and salt water. The body has the flattened sole-like
shape of the Trematode entozoa (Fig. 378, No. 9), the mouth is surrounded
by a circular sucker; this is applied to the surface of the plant from which
the animal draws its nourishment; it is also furnished with a rather long
proboscis, which is probably employed for a similar purpose.
Planariæ multiply by eggs, and by spontaneous fissuration in a transverse
direction, each segment becoming a perfect animal. Professor Agassiz
believes that the infusorial animals, Paramæcium and Kolpoda, are simply
planarian larvæ.
Hirudinidæ, the leech tribe, are usually believed to form a link between the
Annelida on the one hand, and the Trematoda on the other; their affinities
place them closer with the latter than the former. Although deprived of the
characteristic setæ of the Annelida, and exhibiting no sectional divisions,
they are provided with a sucker-like mouth possessed by Trematoda, but
Page 666
they present no resemblance to them in their reproductive organs. On the
other hand, in the arrangement of the nervous system and in their vascular
system, the Hirudinidæ resemble Annelida. The head in most of the
Annelida is distinctly marked, and furnished with eyes, tentacles, mouth,
and teeth, and in some instances with auditory vesicles, containing
otolithes. The nervous system consists of a series of ganglia running along
the ventral portion of the animal, and communicating with a central mass of
brain.
Hirudina medicinalis puts forth a claim for special attention on the ground
of services rendered to mankind. The whole of the family live by sucking
the blood of other animals; and for this purpose the mouth of the leech is
furnished with a number of strong horny teeth, by which they cut through
the skin. In the common leech three rows of teeth exist, arranged in a
triangular, or rather triradiate form, a structure that accounts for the peculiar
appearance of leech bites. The most interesting part of the anatomy of the
leech to microscopists is certainly the structure of the mouth (Fig. 380).
This is a muscular dilatable orifice, within which three beautiful little semi-
circular saws are situated, arranged so that their edges meet in the centre. It
is by means of these saws that the leech makes the incisions whence blood
is to be procured, an operation which is performed in the following manner.
No sooner is the sucker firmly fixed to the skin, than the mouth becomes
slightly everted, and the edges of the saws are thus made to press upon the
tense skin, a sawing movement being at the same time given to each,
whereby it is made gradually to pierce the surface, and cut its way to the
capillary blood-vessels beneath.
In Clepsinidæ the body is of a leech-like form, but
very much narrowed in front, and the mouth is
furnished with a prehensile proboscis. These animals
live in fresh water, where they may often be seen
creeping over aquatic plants. Their prey is the pond-
snail.
Tubicola.—The worms belonging to this series of
branchiferous Annelida are all marine, and
Fig. 380.—Mouth of Leech. distinguished by their invariable habit of forming a
other hand, in the arrangement of the nervous system and in their vascular
system, the Hirudinidæ resemble Annelida. The head in most of the
Annelida is distinctly marked, and furnished with eyes, tentacles, mouth,
and teeth, and in some instances with auditory vesicles, containing
otolithes. The nervous system consists of a series of ganglia running along
the ventral portion of the animal, and communicating with a central mass of
brain.
Hirudina medicinalis puts forth a claim for special attention on the ground
of services rendered to mankind. The whole of the family live by sucking
the blood of other animals; and for this purpose the mouth of the leech is
furnished with a number of strong horny teeth, by which they cut through
the skin. In the common leech three rows of teeth exist, arranged in a
triangular, or rather triradiate form, a structure that accounts for the peculiar
appearance of leech bites. The most interesting part of the anatomy of the
leech to microscopists is certainly the structure of the mouth (Fig. 380).
This is a muscular dilatable orifice, within which three beautiful little semi-
circular saws are situated, arranged so that their edges meet in the centre. It
is by means of these saws that the leech makes the incisions whence blood
is to be procured, an operation which is performed in the following manner.
No sooner is the sucker firmly fixed to the skin, than the mouth becomes
slightly everted, and the edges of the saws are thus made to press upon the
tense skin, a sawing movement being at the same time given to each,
whereby it is made gradually to pierce the surface, and cut its way to the
capillary blood-vessels beneath.
In Clepsinidæ the body is of a leech-like form, but
very much narrowed in front, and the mouth is
furnished with a prehensile proboscis. These animals
live in fresh water, where they may often be seen
creeping over aquatic plants. Their prey is the pond-
snail.
Tubicola.—The worms belonging to this series of
branchiferous Annelida are all marine, and
Fig. 380.—Mouth of Leech. distinguished by their invariable habit of forming a
Page 667
tube or case, within which the soft parts of the animal can be entirely
retracted. This tube is usually attached to stones or other submarine bodies.
Externally it is composed of various foreign materials, sand, crystalline
bodies, and the débris of shells; internally it is lined with a smooth coating
of sarcode, sometimes of a harder consistency. The Tubicola generally live
in societies, winding their tubes into a mass which often attains a
considerable size; only a few are solitary in their habits. They retain their
position in their cases by means of tufts of bristles and spines; the latter, in
the tubicular Annelids, are usually hooked, so that by applying them to the
walls of the case, the animal is enabled to oppose a considerable resistance
to any effort made to withdraw it. In the best known family of the order
(Sabellia), the branchiæ are placed in the head, and form a circle of plumes,
or a tuft of branched organs. The Serpulidæ form irregularly twisted
calcareous tubes, and often grow together in large masses, when they secure
themselves to shells and similar objects; other species, Terebellidæ, which
build their cases of sand and stones, appear to prefer a life of solitude. The
best known form is Terebella littoralis.79 The curious little spiral shells seen
upon the fronds of seaweeds are formed by an animal belonging to the
Spirorbis.
If the animals be placed in a
vessel of sea-water a very
pleasing spectacle will soon be
witnessed. The top part of the
tube is seen to open, and the
creature cautiously protrudes a
fringe of tentacles; these
gradually spread out two
beautiful fan-like rows of
tentacles, surrounded by cilia of a
rich purple or red colour. These
serve the double purpose of
breathing and feeding organs.
When withdrawn from its Fig. 381.—Serpula with extended tentacles and body
protruding from calcareous case.
calcareous case, the soft body is
seen to be constructed of a series
of rings, with a terminal prehensile foot by which it attaches itself.
retracted. This tube is usually attached to stones or other submarine bodies.
Externally it is composed of various foreign materials, sand, crystalline
bodies, and the débris of shells; internally it is lined with a smooth coating
of sarcode, sometimes of a harder consistency. The Tubicola generally live
in societies, winding their tubes into a mass which often attains a
considerable size; only a few are solitary in their habits. They retain their
position in their cases by means of tufts of bristles and spines; the latter, in
the tubicular Annelids, are usually hooked, so that by applying them to the
walls of the case, the animal is enabled to oppose a considerable resistance
to any effort made to withdraw it. In the best known family of the order
(Sabellia), the branchiæ are placed in the head, and form a circle of plumes,
or a tuft of branched organs. The Serpulidæ form irregularly twisted
calcareous tubes, and often grow together in large masses, when they secure
themselves to shells and similar objects; other species, Terebellidæ, which
build their cases of sand and stones, appear to prefer a life of solitude. The
best known form is Terebella littoralis.79 The curious little spiral shells seen
upon the fronds of seaweeds are formed by an animal belonging to the
Spirorbis.
If the animals be placed in a
vessel of sea-water a very
pleasing spectacle will soon be
witnessed. The top part of the
tube is seen to open, and the
creature cautiously protrudes a
fringe of tentacles; these
gradually spread out two
beautiful fan-like rows of
tentacles, surrounded by cilia of a
rich purple or red colour. These
serve the double purpose of
breathing and feeding organs.
When withdrawn from its Fig. 381.—Serpula with extended tentacles and body
protruding from calcareous case.
calcareous case, the soft body is
seen to be constructed of a series
of rings, with a terminal prehensile foot by which it attaches itself.
Page 668
Many Annelids are without tubes or cells of any kind, simply burying their
bodies in the sand near tidal mark. The Arenicola, lob-worm, is a well-
known specimen of the class; its body is so transparent that the circulating
fluids can be distinctly seen under a moderate magnifying power. Two kinds
of fluids flow through the vessels, one nearly colourless, the other red; the
vessels through which the latter circulate are described as blood-vessels.
Not very much interest attaches to the developmental stage of the Annelida.
They issue forth from ova, and the embryo so closely resemble ciliated
polypes, that competent observers have mistaken them for animals
belonging to a lower class; a few hours’ careful watching is sufficient to
dispel a belief of the kind, when the embryonic, globular, or shapeless mass
is seen to assume a form of segmentation, and soon the various internal
organs become more and more developed, eye spots appear, and the young
animal arrives at the adult stage of its existence.
Crustacea.
The crustaceans comprise a large assemblage of Arthropods, presenting
great diversity of structure. Some of the parasitic species have become so
simplified in organisation that they appear to present no relationship with
the higher members of the class, yet it is certain that all the species, whether
terrestrial or aquatic, belong to the same stock, and may have had origin in
the same fundamental plan of structure. Essentially, the body consists of a
large number of segments, to each of which is attached a pair of two-
branched appendages; the external branch is termed the exopodite and the
internal the endopodite. Five segments at the front end of the body unite to
form a head, the appendages of the first two being situated in front of the
mouth, and performing the office of feelers or antennæ, while those of the
remaining three segments are transformed into jaws, the first pair of jaws
being the mandibles and the following two pairs the maxillæ. The rest of the
appendages are variously modified and to some are attached respiratory
organs in the form of gills. Crustaceans are broadly divided from
Centipedes, Millipedes, Insects, &c., by the presence of two pairs instead of
one pair of antennæ, and by the possession of branchial and not tubular
(tracheal) respiratory organs. Arachnida and some other species are again
bodies in the sand near tidal mark. The Arenicola, lob-worm, is a well-
known specimen of the class; its body is so transparent that the circulating
fluids can be distinctly seen under a moderate magnifying power. Two kinds
of fluids flow through the vessels, one nearly colourless, the other red; the
vessels through which the latter circulate are described as blood-vessels.
Not very much interest attaches to the developmental stage of the Annelida.
They issue forth from ova, and the embryo so closely resemble ciliated
polypes, that competent observers have mistaken them for animals
belonging to a lower class; a few hours’ careful watching is sufficient to
dispel a belief of the kind, when the embryonic, globular, or shapeless mass
is seen to assume a form of segmentation, and soon the various internal
organs become more and more developed, eye spots appear, and the young
animal arrives at the adult stage of its existence.
Crustacea.
The crustaceans comprise a large assemblage of Arthropods, presenting
great diversity of structure. Some of the parasitic species have become so
simplified in organisation that they appear to present no relationship with
the higher members of the class, yet it is certain that all the species, whether
terrestrial or aquatic, belong to the same stock, and may have had origin in
the same fundamental plan of structure. Essentially, the body consists of a
large number of segments, to each of which is attached a pair of two-
branched appendages; the external branch is termed the exopodite and the
internal the endopodite. Five segments at the front end of the body unite to
form a head, the appendages of the first two being situated in front of the
mouth, and performing the office of feelers or antennæ, while those of the
remaining three segments are transformed into jaws, the first pair of jaws
being the mandibles and the following two pairs the maxillæ. The rest of the
appendages are variously modified and to some are attached respiratory
organs in the form of gills. Crustaceans are broadly divided from
Centipedes, Millipedes, Insects, &c., by the presence of two pairs instead of
one pair of antennæ, and by the possession of branchial and not tubular
(tracheal) respiratory organs. Arachnida and some other species are again
Page 669
widely separated. The majority of the young on leaving the egg are quite
unlike the parent, and only acquires their definite form after undergoing a
series of changes. The earliest stage, which has been called the Nauplius,
already referred to in connection with the barnacle, is a minute body
showing no trace of segmentation, and provided with a single eye, and three
pairs of swimming appendages, which become the two pairs of antennæ and
the mandibles of the adult. This stage is by no means of invariable
occurrence, but is chiefly characteristic of the lowest members, the
Entomostraca, and is rare in the higher, Malacostraca. The typical
crustaceans are shrimps, crayfish, &c., so familiarly described by Huxley.
The zoæa stage of the crab, a minute transparent creature, which undergoes
several changes, swims about flapping its long jointed abdomen, like some
of the Entomostraca, and the shrimp in particular. The larva of crayfish, the
so-called glass-crab, is very peculiar and interesting. The sessile-eyed
series, in which the compound eyes are never mounted on a movable stalk,
and to which the Isopoda belong, exhibits great diversity of structure as
well as of habits and habitat. Some live in fresh water, most are marine,
while others live on land and take to a parasitic life.
This genus contains Gnathia, in which the male
and female are so dissimilar, that they are
frequently referred to as members of two
families. In the adult male the mandibles are
powerful and prominent, and the head is large,
squared, and as wide as the thorax. In the
female, on the contrary, the head is curiously
small and triangular, without visible mandibles,
and the thorax is much dilated. The creatures
are about one-sixth of an inch long, and of a
greyish colour, and the destruction they bring
about is due to their habit of boring into timber
below water mark. Fig. 382 represents an
enlarged view of the male Gnathia. These Fig. 382.—Male Gnathia, enlarged.
crustaceans are vegetarians, and feed on wood.
Other members of the group, known as fish lice, are much larger in size,
and chiefly infest the cetacea, and bear in addition two large eyes. By
means of their powerful fore feet the Cymothordæ attach themselves to both
unlike the parent, and only acquires their definite form after undergoing a
series of changes. The earliest stage, which has been called the Nauplius,
already referred to in connection with the barnacle, is a minute body
showing no trace of segmentation, and provided with a single eye, and three
pairs of swimming appendages, which become the two pairs of antennæ and
the mandibles of the adult. This stage is by no means of invariable
occurrence, but is chiefly characteristic of the lowest members, the
Entomostraca, and is rare in the higher, Malacostraca. The typical
crustaceans are shrimps, crayfish, &c., so familiarly described by Huxley.
The zoæa stage of the crab, a minute transparent creature, which undergoes
several changes, swims about flapping its long jointed abdomen, like some
of the Entomostraca, and the shrimp in particular. The larva of crayfish, the
so-called glass-crab, is very peculiar and interesting. The sessile-eyed
series, in which the compound eyes are never mounted on a movable stalk,
and to which the Isopoda belong, exhibits great diversity of structure as
well as of habits and habitat. Some live in fresh water, most are marine,
while others live on land and take to a parasitic life.
This genus contains Gnathia, in which the male
and female are so dissimilar, that they are
frequently referred to as members of two
families. In the adult male the mandibles are
powerful and prominent, and the head is large,
squared, and as wide as the thorax. In the
female, on the contrary, the head is curiously
small and triangular, without visible mandibles,
and the thorax is much dilated. The creatures
are about one-sixth of an inch long, and of a
greyish colour, and the destruction they bring
about is due to their habit of boring into timber
below water mark. Fig. 382 represents an
enlarged view of the male Gnathia. These Fig. 382.—Male Gnathia, enlarged.
crustaceans are vegetarians, and feed on wood.
Other members of the group, known as fish lice, are much larger in size,
and chiefly infest the cetacea, and bear in addition two large eyes. By
means of their powerful fore feet the Cymothordæ attach themselves to both
Page 670
marine and fresh-water fish, showing a preference for the inside of the
mouth of their host.
The bar-footed group Copepoda are
free living, and the thorax bears four or
five swimming feet; the abdomen is
without appendages. The best known
fresh-water form is Cyclops, the
structure of which serves as a type of
the order. The body is, as is well
known to microscopists, broad in front
and tapering behind, being thus, when
viewed swimming, pear-shaped in
outline. The dorsal elements of the
head are fused to form a carapace,
which bears a single eye, from which
circumstance it derives its name. The
eggs are carried by the female in a
couple of ova-sacs attached to the last
Fig. 383.—1. Cypris; 2. Cyclops; 3. segment of the thorax, and so prolific
Branchipus grubei.
are these creatures that a female will
produce over four thousand million
young. The young when hatched is an oval Nauplius, which after two or
three moults acquires the adult state. In the family of the Apodidæ we have
an equally well-known crustacean, the Branchipus. In the Branchipodidæ
the body is also elongated, but there are no appendages to the abdomen,
which consists of nine segments, while there are eleven pairs of thoracic
appendages. The head shield is not developed backwards, and the large
separated eyes are supported on distinct stalks. In the male the second
antennæ are converted into claspers. These crustaceans swim upside down
(Fig. 383).
Cladocera (Daphniadæ of Dr. Baird).—The water-flea (Daphnia pulex)
may be taken as the best known example of the order. The body of this little
active animal is narrowed in front, and at the posterior end, where the
carapace is deeply notched, is the tip of the abdomen bearing the pair of
rigid barbed setæ from which the genus takes its name. At the front of the
mouth of their host.
The bar-footed group Copepoda are
free living, and the thorax bears four or
five swimming feet; the abdomen is
without appendages. The best known
fresh-water form is Cyclops, the
structure of which serves as a type of
the order. The body is, as is well
known to microscopists, broad in front
and tapering behind, being thus, when
viewed swimming, pear-shaped in
outline. The dorsal elements of the
head are fused to form a carapace,
which bears a single eye, from which
circumstance it derives its name. The
eggs are carried by the female in a
couple of ova-sacs attached to the last
Fig. 383.—1. Cypris; 2. Cyclops; 3. segment of the thorax, and so prolific
Branchipus grubei.
are these creatures that a female will
produce over four thousand million
young. The young when hatched is an oval Nauplius, which after two or
three moults acquires the adult state. In the family of the Apodidæ we have
an equally well-known crustacean, the Branchipus. In the Branchipodidæ
the body is also elongated, but there are no appendages to the abdomen,
which consists of nine segments, while there are eleven pairs of thoracic
appendages. The head shield is not developed backwards, and the large
separated eyes are supported on distinct stalks. In the male the second
antennæ are converted into claspers. These crustaceans swim upside down
(Fig. 383).
Cladocera (Daphniadæ of Dr. Baird).—The water-flea (Daphnia pulex)
may be taken as the best known example of the order. The body of this little
active animal is narrowed in front, and at the posterior end, where the
carapace is deeply notched, is the tip of the abdomen bearing the pair of
rigid barbed setæ from which the genus takes its name. At the front of the
Page 671
head is a large compound eye and two pairs of branched plumed
appendages, antennæ. The first pair of these are small and simple. The jaws
consist of the mandibles and the first pair of maxillæ, the second pair of
maxillæ being obsolete in the adult. The thorax comprises five segments,
each bearing a pair of leaf-like swimming limbs. The abdomen consists of
three segments, and is destitute of limbs. The males are usually smaller than
the females, and much rarer, being rarely met with before the end of
summer.
Eggs are laid both in summer and winter, and are passed into a brood-
pouch, separating the upper surface of the thorax from the backward
extension of the carapace. Here the summer eggs hatch, but the winter set
are enclosed in a kind of capsule developed from the carapace. This
capsule, termed the ephippium, is cast off with the next moult of the
mother’s integument (a process necessary for the gradual growth of the
crustacean), and falling to the bottom of the water, gives exit to the
embryos, which hatch in its interior, and the young born from these
“ephippial” eggs produce young, which in their turn become mothers. It
appears, then, the winter eggs are enclosed in capsules of more than usual
hardness to enable them to withstand any degree of cold that might
otherwise prove fatal to the parent. Dr. Baird found, on examining ponds
that had been again filled up by rain after remaining two months dry,
numerous specimens of Daphnia and Cyclops quadricornis in all stages of
growth.80
We learn also from his investigations that the Daphnia have many enemies.
“The larva of the Corethra plumicornis, known to microscopical observers
as the skeleton larva, is exceedingly rapacious of Daphnia. Pritchard says
they are the choice food of a species of Nais; and Dr. Parnell states that the
Lochleven trout owes its superior sweetness and richness of flavour to its
food, which consists of small shell-fish and Entomostraca.” These
crustaceans abound in fresh and salt water. Artemiæ are formed exclusively
in salt water, in salt marshes, and in water highly charged with salt. Myriads
of these Entomostraca are found in the salterns at Lymington, in the open
tanks or reservoirs where the brine is deposited previous to boiling. A pint
of the fluid contains about a quarter of a pound of salt, and this concentrated
solution destroys most other marine animals. During the fine days in
appendages, antennæ. The first pair of these are small and simple. The jaws
consist of the mandibles and the first pair of maxillæ, the second pair of
maxillæ being obsolete in the adult. The thorax comprises five segments,
each bearing a pair of leaf-like swimming limbs. The abdomen consists of
three segments, and is destitute of limbs. The males are usually smaller than
the females, and much rarer, being rarely met with before the end of
summer.
Eggs are laid both in summer and winter, and are passed into a brood-
pouch, separating the upper surface of the thorax from the backward
extension of the carapace. Here the summer eggs hatch, but the winter set
are enclosed in a kind of capsule developed from the carapace. This
capsule, termed the ephippium, is cast off with the next moult of the
mother’s integument (a process necessary for the gradual growth of the
crustacean), and falling to the bottom of the water, gives exit to the
embryos, which hatch in its interior, and the young born from these
“ephippial” eggs produce young, which in their turn become mothers. It
appears, then, the winter eggs are enclosed in capsules of more than usual
hardness to enable them to withstand any degree of cold that might
otherwise prove fatal to the parent. Dr. Baird found, on examining ponds
that had been again filled up by rain after remaining two months dry,
numerous specimens of Daphnia and Cyclops quadricornis in all stages of
growth.80
We learn also from his investigations that the Daphnia have many enemies.
“The larva of the Corethra plumicornis, known to microscopical observers
as the skeleton larva, is exceedingly rapacious of Daphnia. Pritchard says
they are the choice food of a species of Nais; and Dr. Parnell states that the
Lochleven trout owes its superior sweetness and richness of flavour to its
food, which consists of small shell-fish and Entomostraca.” These
crustaceans abound in fresh and salt water. Artemiæ are formed exclusively
in salt water, in salt marshes, and in water highly charged with salt. Myriads
of these Entomostraca are found in the salterns at Lymington, in the open
tanks or reservoirs where the brine is deposited previous to boiling. A pint
of the fluid contains about a quarter of a pound of salt, and this concentrated
solution destroys most other marine animals. During the fine days in
Page 672
summer Artemiæ may be observed in immense numbers near the surface of
the water, and, as they are frequently of a lively red colour, the water
appears tinged with the same hue. The movements of this little animal are
peculiar. It swims about on its back, and by means of its tail, its feet being
at the same time in constant motion. They are both oviparous and
ovoviviparous, according to the season of the year. At certain periods they
only lay eggs, while during the hot summer months they produce their
young alive. In about fifteen days the eggs are expelled in numbers varying
from 50 to 150. As is the case with many of the Entomostraca, the young
present a very different appearance from the adult animals; and they are so
exactly like the young of Chirocephalus, that with difficulty are they
distinguishable one from the other. The ova of other species are furnished
with thick capsules, and imbedded in a dark opaque substance, presenting a
minutely cellular appearance, and occupying the interspace between the
body of the animal and the back of the shell; this is called the ephippium.
The shell is often beautifully transparent, sometimes spotted with pigment;
it consists of a substance known as chitine, impregnated with a variable
amount of calcium carbonate, which produces a copious effervescence on
the addition of a small quantity of a strong acid to the water in which the
shell is immersed. When boiled, Artemiæ turn red as their congeners,
lobsters. Their shells may be said to consist of two valves united at the
back, resembling the bivalve shell of a mussel, or simply folded at the back
to appear like a bivalve, but are really not so; or they may consist of a
number of rings or segments. The body of Cypris presents a reticulated
appearance, somewhat resembling cell structure. Entomostraca should be
narcotised and prepared for examination under the microscope as directed
by Mr. Rousselet at pages 345, 346.
Insects’ Eggs, etc.
the water, and, as they are frequently of a lively red colour, the water
appears tinged with the same hue. The movements of this little animal are
peculiar. It swims about on its back, and by means of its tail, its feet being
at the same time in constant motion. They are both oviparous and
ovoviviparous, according to the season of the year. At certain periods they
only lay eggs, while during the hot summer months they produce their
young alive. In about fifteen days the eggs are expelled in numbers varying
from 50 to 150. As is the case with many of the Entomostraca, the young
present a very different appearance from the adult animals; and they are so
exactly like the young of Chirocephalus, that with difficulty are they
distinguishable one from the other. The ova of other species are furnished
with thick capsules, and imbedded in a dark opaque substance, presenting a
minutely cellular appearance, and occupying the interspace between the
body of the animal and the back of the shell; this is called the ephippium.
The shell is often beautifully transparent, sometimes spotted with pigment;
it consists of a substance known as chitine, impregnated with a variable
amount of calcium carbonate, which produces a copious effervescence on
the addition of a small quantity of a strong acid to the water in which the
shell is immersed. When boiled, Artemiæ turn red as their congeners,
lobsters. Their shells may be said to consist of two valves united at the
back, resembling the bivalve shell of a mussel, or simply folded at the back
to appear like a bivalve, but are really not so; or they may consist of a
number of rings or segments. The body of Cypris presents a reticulated
appearance, somewhat resembling cell structure. Entomostraca should be
narcotised and prepared for examination under the microscope as directed
by Mr. Rousselet at pages 345, 346.
Insects’ Eggs, etc.
Page 673
Tuffen West, del. Edmund Evans.
Plate VI.
Plate VI.
Page 674
CHAPTER IV.
Arthropoda—Insecta.
Distinctive Characters of Insects.—The term Insect, although originally and
according to the meaning of the word correctly employed in a wide sense to
embrace all those articulate creatures in which the body is externally
divided into a number of segments, including, of course, flies, butterflies,
beetles, bugs, spiders, scorpions, crabs, shrimps, &c., is now by common
consent used in a much more restricted sense to apply only to such of these
animals as have six walking legs. Insects belong to a class of Arthropoda,
and are distinguished by having the head, chest, and abdomen distinctly
marked out and separable; by having not more than three pairs of legs in the
adult state; by having the legs borne by the thoracic segments only; by
having usually two pairs of wings; by the possession of tracheæ, or air-
tubes, as respiratory organs; and by being provided with a single pair of
antennæ, or feelers. The insect class is one exhibiting uniformity of type
and structure. Extreme variations are no doubt seen within certain limits,
but these variations are sharply marked off from the groups we have been
previously considering. The examination of insects may be pursued
according to a defined order, and it will be found that no class of animals
will afford the microscopist a more wonderful field of observation and a
greater variety of interesting objects than that of the insect tribes.
In the insect, as in the crustacean, the hard parts of the body form an outer
and protecting covering, and also serve for the attachment of muscles. The
casing, however, in insects is purely of a chitinous, or horny nature, and has
in its composition only a trace of calcium carbonate. Each somite, or joint
of the body, is usually composed of six pieces; the upper, or dorsal half of
each segment is named the tergum, the lower half the sternum, the side
pieces pleura, the sternum being further sub-divided into epimeral and
espisternal pieces. The body as a whole consists of some twenty segments,
Arthropoda—Insecta.
Distinctive Characters of Insects.—The term Insect, although originally and
according to the meaning of the word correctly employed in a wide sense to
embrace all those articulate creatures in which the body is externally
divided into a number of segments, including, of course, flies, butterflies,
beetles, bugs, spiders, scorpions, crabs, shrimps, &c., is now by common
consent used in a much more restricted sense to apply only to such of these
animals as have six walking legs. Insects belong to a class of Arthropoda,
and are distinguished by having the head, chest, and abdomen distinctly
marked out and separable; by having not more than three pairs of legs in the
adult state; by having the legs borne by the thoracic segments only; by
having usually two pairs of wings; by the possession of tracheæ, or air-
tubes, as respiratory organs; and by being provided with a single pair of
antennæ, or feelers. The insect class is one exhibiting uniformity of type
and structure. Extreme variations are no doubt seen within certain limits,
but these variations are sharply marked off from the groups we have been
previously considering. The examination of insects may be pursued
according to a defined order, and it will be found that no class of animals
will afford the microscopist a more wonderful field of observation and a
greater variety of interesting objects than that of the insect tribes.
In the insect, as in the crustacean, the hard parts of the body form an outer
and protecting covering, and also serve for the attachment of muscles. The
casing, however, in insects is purely of a chitinous, or horny nature, and has
in its composition only a trace of calcium carbonate. Each somite, or joint
of the body, is usually composed of six pieces; the upper, or dorsal half of
each segment is named the tergum, the lower half the sternum, the side
pieces pleura, the sternum being further sub-divided into epimeral and
espisternal pieces. The body as a whole consists of some twenty segments,
Page 675
of which five or six form the head, the thorax of three joints, while the
abdomen may number from nine to eleven. The head segments are united to
form apparently a single mass, and the appendages of this region are
modified for sensory purposes, and also serve as cutting and masticatory
organs. The appendages of the head, examined in order, will be found to
consist of eyes, antennæ, or feelers, and organs of the mouth. The antennæ
of insects rarely exceed two in number, but these present great variations in
form and size. In their simplest form they exist as straight jointed filaments,
but in many insects they are forked, in others club-shaped, while in others
they mimic forms of vegetation, and for the most part are extremely
interesting objects for the microscope.
The principal use of these antennæ is
that of organs of touch, but it is quite
probable that they may subserve other
functions, as of taste or even hearing.
The eyes of insects consist of either a
pair of ocelli, or of a great number,
when they are termed compound eyes,
formed of an aggregation of external
Fig. 384.—Vertical section of cornea of Eye of
hexagonal facets and lenses, and nerve
Fly. filaments, all of which have a distinct
connection with the mass of ganglia
recognised as the brain, as will be seen in Fig. 384, a section of the eye of a
fly. The number of facets varies very greatly in these compound eyes; ants,
for example, have fifty facets, flies two thousand or more, and butterflies as
many. Dr. Hooke counted seven thousand, and Leuwenhoeck as many as
twelve thousand in the eye of a dragon fly. The eyes of some insects are
supported on short stalks or pedicles, but these are never movable, as, for
example, in Stalk-eyed crustaceans.
The organs of the mouth in insects present a striking homology or similarity
in their fundamental structure. Two chief types of mouth are found. The
biting or masticatory, as in beetles, includes a labium or upper lip, a pair of
mandibles or lower jaws, a pair of lesser jaws or maxillæ, which bear one or
two pairs of palpi, and a lower lip or labium, also with palpi. This latter and
primitive condition of the labium is seen in Orthropterous insects and some
abdomen may number from nine to eleven. The head segments are united to
form apparently a single mass, and the appendages of this region are
modified for sensory purposes, and also serve as cutting and masticatory
organs. The appendages of the head, examined in order, will be found to
consist of eyes, antennæ, or feelers, and organs of the mouth. The antennæ
of insects rarely exceed two in number, but these present great variations in
form and size. In their simplest form they exist as straight jointed filaments,
but in many insects they are forked, in others club-shaped, while in others
they mimic forms of vegetation, and for the most part are extremely
interesting objects for the microscope.
The principal use of these antennæ is
that of organs of touch, but it is quite
probable that they may subserve other
functions, as of taste or even hearing.
The eyes of insects consist of either a
pair of ocelli, or of a great number,
when they are termed compound eyes,
formed of an aggregation of external
Fig. 384.—Vertical section of cornea of Eye of
hexagonal facets and lenses, and nerve
Fly. filaments, all of which have a distinct
connection with the mass of ganglia
recognised as the brain, as will be seen in Fig. 384, a section of the eye of a
fly. The number of facets varies very greatly in these compound eyes; ants,
for example, have fifty facets, flies two thousand or more, and butterflies as
many. Dr. Hooke counted seven thousand, and Leuwenhoeck as many as
twelve thousand in the eye of a dragon fly. The eyes of some insects are
supported on short stalks or pedicles, but these are never movable, as, for
example, in Stalk-eyed crustaceans.
The organs of the mouth in insects present a striking homology or similarity
in their fundamental structure. Two chief types of mouth are found. The
biting or masticatory, as in beetles, includes a labium or upper lip, a pair of
mandibles or lower jaws, a pair of lesser jaws or maxillæ, which bear one or
two pairs of palpi, and a lower lip or labium, also with palpi. This latter and
primitive condition of the labium is seen in Orthropterous insects and some
Page 676
Neuroptera. Other structures occurring in those of the mouth are the ligula,
this being sometimes divided, as in bees, into three lobes, of which the two
outer are the paraglossæ and the middle process the lingua or tongue. There
is a second form of mouth, termed the suctorial. This is seen in Lepidoptera
(butterflies), and is adapted for extracting the pollen and juices of flowers,
and in which the palpi are greatly developed, and form two hairy pads or
cushions, between which the proboscis is coiled up when at rest. Thus we
find in the Lepidoptera the same fundamental condition of mouth as in
some Coleoptera. In Hymenoptera (wasps and bees), a variety of mouth is
found which presents a combination of the masticatory with the suctorial
types. The labium and mandibles exist as in the beetle, the maxillæ being
developed to form long sheaths protecting the labium, which now takes the
form of a tongue. In Hemiptera (bugs and their allies), the mandibles and
maxillæ exist as sharp lancets, while the labium forms a protective sheath.
In the Diptera (flies, gnats, &c.), the labium undergoes a great development,
and forms a very prominent tongue, the other parts of the mouth being
developed simply as sheaths to the labium. See Figs. 389 and 390.
The thorax or chest of insects consists of three segments, named from
before backwards: the prothorax, mesothorax, and metathorax. The first
bears the anterior pair of legs; the mesothorax, the second pair of legs and
the first pair of wings; and the metathorax, the third pair of legs and second
pair of wings. The last joints of the leg constitute the tarsus or foot-claws.
The nervures of the wings are in reality hollow tubes, and are extensions of
the spiracles, or respiratory apertures.
The muscles of insects lie concealed beneath the integument; they are not
gathered into distinct bundles as in the higher animals, although they
exhibit in many cases a striated or striped structure. This is well seen in
some of the beetle tribe, the water-beetle in particular. In certain larvæ the
muscles are exceedingly complicated. Lyonnet found in the larva of the
goat-moth, two hundred and twenty-eight muscles in the head alone, and in
the whole body no less than three thousand nine hundred and ninety-three.
The muscular power of insects is, relatively to the size of the body, very
great. The flea, for instance, leaps two hundred times its own height. There
are beetles weighing a few grammes that will escape from a pressure of
from twenty to thirty ounces.
this being sometimes divided, as in bees, into three lobes, of which the two
outer are the paraglossæ and the middle process the lingua or tongue. There
is a second form of mouth, termed the suctorial. This is seen in Lepidoptera
(butterflies), and is adapted for extracting the pollen and juices of flowers,
and in which the palpi are greatly developed, and form two hairy pads or
cushions, between which the proboscis is coiled up when at rest. Thus we
find in the Lepidoptera the same fundamental condition of mouth as in
some Coleoptera. In Hymenoptera (wasps and bees), a variety of mouth is
found which presents a combination of the masticatory with the suctorial
types. The labium and mandibles exist as in the beetle, the maxillæ being
developed to form long sheaths protecting the labium, which now takes the
form of a tongue. In Hemiptera (bugs and their allies), the mandibles and
maxillæ exist as sharp lancets, while the labium forms a protective sheath.
In the Diptera (flies, gnats, &c.), the labium undergoes a great development,
and forms a very prominent tongue, the other parts of the mouth being
developed simply as sheaths to the labium. See Figs. 389 and 390.
The thorax or chest of insects consists of three segments, named from
before backwards: the prothorax, mesothorax, and metathorax. The first
bears the anterior pair of legs; the mesothorax, the second pair of legs and
the first pair of wings; and the metathorax, the third pair of legs and second
pair of wings. The last joints of the leg constitute the tarsus or foot-claws.
The nervures of the wings are in reality hollow tubes, and are extensions of
the spiracles, or respiratory apertures.
The muscles of insects lie concealed beneath the integument; they are not
gathered into distinct bundles as in the higher animals, although they
exhibit in many cases a striated or striped structure. This is well seen in
some of the beetle tribe, the water-beetle in particular. In certain larvæ the
muscles are exceedingly complicated. Lyonnet found in the larva of the
goat-moth, two hundred and twenty-eight muscles in the head alone, and in
the whole body no less than three thousand nine hundred and ninety-three.
The muscular power of insects is, relatively to the size of the body, very
great. The flea, for instance, leaps two hundred times its own height. There
are beetles weighing a few grammes that will escape from a pressure of
from twenty to thirty ounces.
Page 677
Professor Schäfer infers that the structure of the wing-muscles of insects
furnishes the key to the comprehension of the more intricate muscular
structure of vertebrates. The sarcode element, however, is not made up of a
bundle of rods, but of a continuous sarcous element, readily made out by
staining with hæmatoxylin. This substance is then seen to be pierced by
minute tubular canals, and the longitudinal striation of muscle is due to this
canalisation. The whole is connected and enclosed by a membrane of
extreme delicacy.
The digestive system of insects varies with their habits and food. In Stylops,
bee-parasites, and in young bees living on fluids, the intestine ends in a
blind sac. There are three coats of structure throughout the digestive system.
The œsophagus or gullet is provided with a crop in flies, bees, and
butterflies; a true analogue of the gizzard in birds. There is in some respects
a curious likeness between the conformation of the digestive organs of birds
and that of insects. No true liver, but salivary glands in the mouth have been
made out; the heart lies dorsally, and consists of a pulsating sac divided into
compartments, and the fluid flows through it towards the head, whence it
circulates freely to other parts of the body. Each trachea is an elastic tube
formed of two delicate membranes, between which the spiral filament is
coiled up, and is of sufficient density to prevent the collapse of the tube by
the movements of the body. These tracheæ are distributed throughout the
muscular tissue and the whole of the body. Thus the insect, like the bird,
may be said to breathe in every part of the body, and is in this way rendered
light and buoyant for flight. The air is admitted to the tracheæ by apertures
termed spiracles, which the insect can close at will, and these are distributed
to the number of eleven on each side of the body. The nervous system
consists of a chain of ganglia or nerve-knots, which unite towards the head
to form a single cord, as seen in the section made through the spider (Fig.
409).
The reproduction of all insects takes place by ova, and they are diæceous—
that is, have two distinct sexes. In some few instances, as that of Aphides,
or plant-lice, we have the peculiar phenomenon of parthenogenesis, the
process of reproduction being performed by imperfect wingless females.
These bring forth living young ones, which begin to feed the moment they
are born, and constitute a viviparous brood; in other cases females lay eggs,
furnishes the key to the comprehension of the more intricate muscular
structure of vertebrates. The sarcode element, however, is not made up of a
bundle of rods, but of a continuous sarcous element, readily made out by
staining with hæmatoxylin. This substance is then seen to be pierced by
minute tubular canals, and the longitudinal striation of muscle is due to this
canalisation. The whole is connected and enclosed by a membrane of
extreme delicacy.
The digestive system of insects varies with their habits and food. In Stylops,
bee-parasites, and in young bees living on fluids, the intestine ends in a
blind sac. There are three coats of structure throughout the digestive system.
The œsophagus or gullet is provided with a crop in flies, bees, and
butterflies; a true analogue of the gizzard in birds. There is in some respects
a curious likeness between the conformation of the digestive organs of birds
and that of insects. No true liver, but salivary glands in the mouth have been
made out; the heart lies dorsally, and consists of a pulsating sac divided into
compartments, and the fluid flows through it towards the head, whence it
circulates freely to other parts of the body. Each trachea is an elastic tube
formed of two delicate membranes, between which the spiral filament is
coiled up, and is of sufficient density to prevent the collapse of the tube by
the movements of the body. These tracheæ are distributed throughout the
muscular tissue and the whole of the body. Thus the insect, like the bird,
may be said to breathe in every part of the body, and is in this way rendered
light and buoyant for flight. The air is admitted to the tracheæ by apertures
termed spiracles, which the insect can close at will, and these are distributed
to the number of eleven on each side of the body. The nervous system
consists of a chain of ganglia or nerve-knots, which unite towards the head
to form a single cord, as seen in the section made through the spider (Fig.
409).
The reproduction of all insects takes place by ova, and they are diæceous—
that is, have two distinct sexes. In some few instances, as that of Aphides,
or plant-lice, we have the peculiar phenomenon of parthenogenesis, the
process of reproduction being performed by imperfect wingless females.
These bring forth living young ones, which begin to feed the moment they
are born, and constitute a viviparous brood; in other cases females lay eggs,
Page 678
and the process proceeds in the ordinary way, and nearly all the year round.
The former is provided with a lancet-like beak for piercing and sucking the
juices of the leaf, and a pair of curious honey-tubes. Insects generally
undergo a transformation or metamorphosis in passing from the egg to the
adult stage. While within the egg the body may be seen to become
segmented, and in the course of time—in such insects as flies, bees, beetles,
and butterflies—issue forth from the egg as larvæ, or caterpillars. This
worm-like creature makes for itself an investing case or cocoon, in which it
passes into the pupa stage of its existence. Within the pupa case a wonderful
transformation takes place; the larval body being literally broken down by
the process of histolysis, while its elements are rebuilt and transformed into
that of the imago, or perfect insect. In grasshoppers, crickets, dragon-flies,
bugs, &c., the metamorphosis is incomplete (hemimetabolic). Some few
lower insect forms (lice, spring-tails, &c.) undergo no change of the kind,
and in no way differ from the adult except in size. These are termed
ametabolic insects. Others again, as the cockchafer and gold beetle, pass
three years in the larval stage. Development in all cases is arrested or
retarded by cold. Reaumur kept a butterfly pupa for two years in an ice-
house, and it exhibited no tendency towards a change until removed to a
warm temperature.
From the short natural history of insect life I have endeavoured to sketch
out, it will have been surmised that insects offer a wide field of research,
and an almost endless number of objects of interest for the microscope. The
variety of material is great, and the structure and adaptation of means to an
end is of the most fascinating kind. Most cabinets abound in preparations
gathered together with some care and mounted with all the skill at the
command of the collector, affording, as a rule, as endless an amount of
pleasure to the tyro as to the more practised entomologist. It may be
surmised, then, that to enter fully into a description of the several parts of
insect structure would require a volume81 of very large bulk, and occupy
months and years. I will, therefore, take some points of interest in the
structural characteristics of insects, and take them in the order in which they
have already been brought to notice. The head, eyes, and other appendages
of these insects we are more or less acquainted with.
The former is provided with a lancet-like beak for piercing and sucking the
juices of the leaf, and a pair of curious honey-tubes. Insects generally
undergo a transformation or metamorphosis in passing from the egg to the
adult stage. While within the egg the body may be seen to become
segmented, and in the course of time—in such insects as flies, bees, beetles,
and butterflies—issue forth from the egg as larvæ, or caterpillars. This
worm-like creature makes for itself an investing case or cocoon, in which it
passes into the pupa stage of its existence. Within the pupa case a wonderful
transformation takes place; the larval body being literally broken down by
the process of histolysis, while its elements are rebuilt and transformed into
that of the imago, or perfect insect. In grasshoppers, crickets, dragon-flies,
bugs, &c., the metamorphosis is incomplete (hemimetabolic). Some few
lower insect forms (lice, spring-tails, &c.) undergo no change of the kind,
and in no way differ from the adult except in size. These are termed
ametabolic insects. Others again, as the cockchafer and gold beetle, pass
three years in the larval stage. Development in all cases is arrested or
retarded by cold. Reaumur kept a butterfly pupa for two years in an ice-
house, and it exhibited no tendency towards a change until removed to a
warm temperature.
From the short natural history of insect life I have endeavoured to sketch
out, it will have been surmised that insects offer a wide field of research,
and an almost endless number of objects of interest for the microscope. The
variety of material is great, and the structure and adaptation of means to an
end is of the most fascinating kind. Most cabinets abound in preparations
gathered together with some care and mounted with all the skill at the
command of the collector, affording, as a rule, as endless an amount of
pleasure to the tyro as to the more practised entomologist. It may be
surmised, then, that to enter fully into a description of the several parts of
insect structure would require a volume81 of very large bulk, and occupy
months and years. I will, therefore, take some points of interest in the
structural characteristics of insects, and take them in the order in which they
have already been brought to notice. The head, eyes, and other appendages
of these insects we are more or less acquainted with.
Page 679
We will take for examination a
typical member of Muscidæ, a
family embracing a large and
varied assortment of species,
among which the house-fly and
the blow-fly are the best known
forms. Musca domestica needs
no description. An interesting
part of the house-fly to the
microscopist is the wonderful
component parts of the head. On
examination we find a couple of
protuberances, more or less
prominent, and situated
symmetrically one on each side.
Fig. 385.—A tangential or side section of Eye of Fly, Their outline at the base is for the
with palp or pads protruded. most part oval, elliptical, circular,
or truncated; while their curved
surfaces are spherical, spheroidal, or pyriform. These horny, round, and
naked parts are the corneæ of the compound eye of the fly, and they are
appropriately so termed, from the analogy they bear to the larger transparent
tunics in the higher classes of animals. They differ, however, from the latter,
as when viewed by the microscope they display a large number of
hexagonal facets, which constitute the medium for the admission of light to
several hundred simple eyes. Under an ordinary lens, and by reflected light,
the entire surface of one cornea presents a beautiful reticulation, like very
fine wire gauze, with minute papilla, or at least a slight elevation, in the
centre of each mesh. These are resolved, however, by the aid of a
compound microscope, and with a power of from 80 to 100 diameters, into
an almost incredible number (when compared with the space they occupy)
of minute, regular, geometrical hexagons, well defined, and capable of
being computed with tolerable ease, their exceeding minuteness being taken
into consideration.
Fig. 386 represents a vertical section of the eye, showing the hexagonal
faceted arrangement of cylindrical tubes.
typical member of Muscidæ, a
family embracing a large and
varied assortment of species,
among which the house-fly and
the blow-fly are the best known
forms. Musca domestica needs
no description. An interesting
part of the house-fly to the
microscopist is the wonderful
component parts of the head. On
examination we find a couple of
protuberances, more or less
prominent, and situated
symmetrically one on each side.
Fig. 385.—A tangential or side section of Eye of Fly, Their outline at the base is for the
with palp or pads protruded. most part oval, elliptical, circular,
or truncated; while their curved
surfaces are spherical, spheroidal, or pyriform. These horny, round, and
naked parts are the corneæ of the compound eye of the fly, and they are
appropriately so termed, from the analogy they bear to the larger transparent
tunics in the higher classes of animals. They differ, however, from the latter,
as when viewed by the microscope they display a large number of
hexagonal facets, which constitute the medium for the admission of light to
several hundred simple eyes. Under an ordinary lens, and by reflected light,
the entire surface of one cornea presents a beautiful reticulation, like very
fine wire gauze, with minute papilla, or at least a slight elevation, in the
centre of each mesh. These are resolved, however, by the aid of a
compound microscope, and with a power of from 80 to 100 diameters, into
an almost incredible number (when compared with the space they occupy)
of minute, regular, geometrical hexagons, well defined, and capable of
being computed with tolerable ease, their exceeding minuteness being taken
into consideration.
Fig. 386 represents a vertical section of the eye, showing the hexagonal
faceted arrangement of cylindrical tubes.
Page 680
Fig. 386.—Section of Eye of Fly.
l. Lenses; co. Cones; pl. Pigment layer, consisting of rings round the rods; r.r.
Rods; a.v1. Air vessels between the rods; m1. Membrane on which the rods and air
vessels rest; a.v2. Shorter lengths of air vessels which form a layer above the first
nerve junction; n.j1. First nerve junction; m2. Membrane on which it stands; A. V.,
A. V. Large air vessel surrounding the eye; n.j2. Second nerve junction; a.v3. Air
vessels; op. n. Optic nerve; b.n. Brain substance. (Magnified × 160.)
In this section it appears to be questionable whether the normal shape of the
lenses is not round, assuming the hexagonal shape during the process of
growth in consequence of their agglomeration. The corneal surface can be
peeled off, and if carefully flattened out and mounted it will be seen that
each lens is not a simple lens, but a double-convex compound one,
composed of two plano-convex lenses of different densities or refracting
power joined together.
Experiments made on the eyes of insects, and also of crustaceæ, show that
in the insect a real and reversed image of external bodies is formed in each
ommatidium; it coincides with the internal face of the crystalline cone in
immediate contact with the retina. Although small, the retinal image is
distinct and subtends an angle of nearly forty-five. In the same way in the
crustacean, the crystalline lens forms on the retinula a reversed image, but
the refractive media have a longer focus, and the retinal membrane is not
l. Lenses; co. Cones; pl. Pigment layer, consisting of rings round the rods; r.r.
Rods; a.v1. Air vessels between the rods; m1. Membrane on which the rods and air
vessels rest; a.v2. Shorter lengths of air vessels which form a layer above the first
nerve junction; n.j1. First nerve junction; m2. Membrane on which it stands; A. V.,
A. V. Large air vessel surrounding the eye; n.j2. Second nerve junction; a.v3. Air
vessels; op. n. Optic nerve; b.n. Brain substance. (Magnified × 160.)
In this section it appears to be questionable whether the normal shape of the
lenses is not round, assuming the hexagonal shape during the process of
growth in consequence of their agglomeration. The corneal surface can be
peeled off, and if carefully flattened out and mounted it will be seen that
each lens is not a simple lens, but a double-convex compound one,
composed of two plano-convex lenses of different densities or refracting
power joined together.
Experiments made on the eyes of insects, and also of crustaceæ, show that
in the insect a real and reversed image of external bodies is formed in each
ommatidium; it coincides with the internal face of the crystalline cone in
immediate contact with the retina. Although small, the retinal image is
distinct and subtends an angle of nearly forty-five. In the same way in the
crustacean, the crystalline lens forms on the retinula a reversed image, but
the refractive media have a longer focus, and the retinal membrane is not
Page 681
connected with the lens, the interval being filled up by a substance
analogous to the vitreous of vertebrates. In both cases it would appear that
light does not act directly on the rods; these latter can only receive
impressions through the intermediary retinal cells. The retinal images of
arthropods, as might have been surmised, are much less perfect than those
of the higher orders; on the other hand, their eyes seem to be better adapted
for seeing objects in relief and the movements of bodies. The shyness of
butterflies and moths is certainly an inherited instinct as a protection against
danger from their many enemies.
In the accompanying Fig. 387, A is a
vertical section of the eye of
Melolontha vulgans, the fan-like
arrangement of the facets, together
with the transparent pyramidal
gathering of the retinal rods
proceeding towards the brain; B is a
few of the corneal tubes more highly
Fig. 387. magnified, the darker portion
representing the pigment layer of the
A. Vertical section of Eye of Melolontha vulgans,
Cockchafer; B. A few facets more highly corneal tubes. In Plate VI., No. 133,
magnified, showing facets and pigment layer. the under surface of the head and
mouth of the “Tsetse” fly, Glossina
morsitans, is shown. The proboscis of this fly is long and prominent, and
the antennæ are peculiar, inasmuch as the third segment is long, and
produced almost as far as the flagellum, which is furnished with barbed
hairs along its outer surface only. Although this fly barely equals the blow-
fly in size, it is one of the greatest pests to the domestic cattle of Equatorial
Africa. The palpi, although arising from two roots, are seen joined together
when the fly is at rest, but when in the act of piercing or sucking they divide
and the sheath is thrown directly upwards. The palpi are furnished on their
convex sides with long and sharply-pointed dark-brown setæ or hairs, while
the inner concave sides, which are brought into contact with the proboscis,
are perfectly smooth and fleshy. Three circular openings seem to indicate
the tubular nature of what in the house-fly is a fleshy, expanded, and highly-
developed muscular proboscis (seen in Fig. 388, Musca domestica). The
proboscis (labium) forms the chief part of the organ, dilates into wonderful
analogous to the vitreous of vertebrates. In both cases it would appear that
light does not act directly on the rods; these latter can only receive
impressions through the intermediary retinal cells. The retinal images of
arthropods, as might have been surmised, are much less perfect than those
of the higher orders; on the other hand, their eyes seem to be better adapted
for seeing objects in relief and the movements of bodies. The shyness of
butterflies and moths is certainly an inherited instinct as a protection against
danger from their many enemies.
In the accompanying Fig. 387, A is a
vertical section of the eye of
Melolontha vulgans, the fan-like
arrangement of the facets, together
with the transparent pyramidal
gathering of the retinal rods
proceeding towards the brain; B is a
few of the corneal tubes more highly
Fig. 387. magnified, the darker portion
representing the pigment layer of the
A. Vertical section of Eye of Melolontha vulgans,
Cockchafer; B. A few facets more highly corneal tubes. In Plate VI., No. 133,
magnified, showing facets and pigment layer. the under surface of the head and
mouth of the “Tsetse” fly, Glossina
morsitans, is shown. The proboscis of this fly is long and prominent, and
the antennæ are peculiar, inasmuch as the third segment is long, and
produced almost as far as the flagellum, which is furnished with barbed
hairs along its outer surface only. Although this fly barely equals the blow-
fly in size, it is one of the greatest pests to the domestic cattle of Equatorial
Africa. The palpi, although arising from two roots, are seen joined together
when the fly is at rest, but when in the act of piercing or sucking they divide
and the sheath is thrown directly upwards. The palpi are furnished on their
convex sides with long and sharply-pointed dark-brown setæ or hairs, while
the inner concave sides, which are brought into contact with the proboscis,
are perfectly smooth and fleshy. Three circular openings seem to indicate
the tubular nature of what in the house-fly is a fleshy, expanded, and highly-
developed muscular proboscis (seen in Fig. 388, Musca domestica). The
proboscis (labium) forms the chief part of the organ, dilates into wonderful
Page 682
muscular lips, and enables the insect to employ the tongue as a prehensile
organ. The lips are covered with rows of minute setæ, directed a little
backwards and arranged rather closely together.
Fig. 388.—Proboscis of House-fly, Musca domestica. (The small circle indicates
the object about the natural size.)
There are very many rows of these minute hairs on each of the lips, and
from being arranged in a similar direction are employed by the insect in
scraping or tearing delicate surfaces. These hairs are tests for the best of
high powers. It is by means of these that it teases human beings in the heat
of summer, when it alights on the hand or face, to sip the perspiration as it
exudes from the skin. The fluid ascends the proboscis, partly by a sucking
action, assisted by the muscles of the lips themselves, which are of a spiral
organ. The lips are covered with rows of minute setæ, directed a little
backwards and arranged rather closely together.
Fig. 388.—Proboscis of House-fly, Musca domestica. (The small circle indicates
the object about the natural size.)
There are very many rows of these minute hairs on each of the lips, and
from being arranged in a similar direction are employed by the insect in
scraping or tearing delicate surfaces. These hairs are tests for the best of
high powers. It is by means of these that it teases human beings in the heat
of summer, when it alights on the hand or face, to sip the perspiration as it
exudes from the skin. The fluid ascends the proboscis, partly by a sucking
action, assisted by the muscles of the lips themselves, which are of a spiral
Page 683
form, arranged around a highly elastic, tendinous, and ligamentous
structure, with other retractile additions for rapidity and facility of motion.
The beautiful form of the spiral
structure of the tongue should be
viewed under a high magnifying
power, when it will be seen that
no continuing spiral structure
really exists; each ring,
apparently detached, does not
extend quite round; their action is
that of sucking tubes. Fluids are
evidently drawn up through the
entire fissure caused by the
opening between the ends of the
whole series of rings. It may well
be pronounced a marvellous
Fig. 389.—Spiral structure of Tongue of House-fly,
from a micro-photograph made with a Zeiss 16
structure. The mounting of the
mm. and apochromatic projection eye-piece × tongue must be done with a
150. considerable amount of care to
show this structure, imperfectly
represented in my woodcut.
These insects are of some service in the economy of nature, by their
consumption of decaying animal matter, found about in quantities ordinarily
imperceptible to most people, and that would not be removed by ordinary
means during hot weather. It was asserted by Linnæus that three flies would
consume a dead horse as quickly as a lion. This was, of course, said with
reference to the offspring of such three flies; and it is quite possible the
assertion may be correct, since the young begin to eat as soon as hatched,
and a female blow-fly will produce twenty thousand living larvæ (one of
which is represented in Plate VI., No. 141). In twenty-four hours, each will
have increased in weight two hundred times, in five days it attains to its full
size, and changes into the pupa, and then to the perfect insect.
structure, with other retractile additions for rapidity and facility of motion.
The beautiful form of the spiral
structure of the tongue should be
viewed under a high magnifying
power, when it will be seen that
no continuing spiral structure
really exists; each ring,
apparently detached, does not
extend quite round; their action is
that of sucking tubes. Fluids are
evidently drawn up through the
entire fissure caused by the
opening between the ends of the
whole series of rings. It may well
be pronounced a marvellous
Fig. 389.—Spiral structure of Tongue of House-fly,
from a micro-photograph made with a Zeiss 16
structure. The mounting of the
mm. and apochromatic projection eye-piece × tongue must be done with a
150. considerable amount of care to
show this structure, imperfectly
represented in my woodcut.
These insects are of some service in the economy of nature, by their
consumption of decaying animal matter, found about in quantities ordinarily
imperceptible to most people, and that would not be removed by ordinary
means during hot weather. It was asserted by Linnæus that three flies would
consume a dead horse as quickly as a lion. This was, of course, said with
reference to the offspring of such three flies; and it is quite possible the
assertion may be correct, since the young begin to eat as soon as hatched,
and a female blow-fly will produce twenty thousand living larvæ (one of
which is represented in Plate VI., No. 141). In twenty-four hours, each will
have increased in weight two hundred times, in five days it attains to its full
size, and changes into the pupa, and then to the perfect insect.
Page 684
Fig. 390.—Tongue, Proboscis, and piercing apparatus of Drone-fly (Eristalis
tenax).
tenax).
Page 685
Fig. 391.—Under-surface of a Wasp’s Tongue, Feelers, &c. (Seen within the circle
is the tongue about life-size.)
In the drone-fly (Eristalis tenax), the mouth organs are larger than in the
house-fly, and differ in many respects. The tongue is split up for a certain
distance, and then again united, as represented in Fig. 390. The labium,
mandibles, and maxillæ are converted into well-developed lancet-shaped
organs; these both pierce the skin of animals, and form tubes by which their
blood may be sucked up. Next to the maxillary palpi a couple of lancets are
seen to project out; these again are associated with two other instruments,
one resembling in appearance a two-edged sword, and a peculiar one with
pincers or cutting teeth at the extremity. It is very peculiar, and resembles an
instrument used in surgery for enlarging the wound, and in this case to
increase the flow of blood. This remarkable compound piercing apparatus
of the drone-fly is of exquisite finish, and must strike the observer with
amazement, while it greatly transcends the work of human mechanism. The
fleshy tongue itself projects some distance from the apparatus described,
and is furnished with setæ or hairs, shorter and fewer in number than those
is the tongue about life-size.)
In the drone-fly (Eristalis tenax), the mouth organs are larger than in the
house-fly, and differ in many respects. The tongue is split up for a certain
distance, and then again united, as represented in Fig. 390. The labium,
mandibles, and maxillæ are converted into well-developed lancet-shaped
organs; these both pierce the skin of animals, and form tubes by which their
blood may be sucked up. Next to the maxillary palpi a couple of lancets are
seen to project out; these again are associated with two other instruments,
one resembling in appearance a two-edged sword, and a peculiar one with
pincers or cutting teeth at the extremity. It is very peculiar, and resembles an
instrument used in surgery for enlarging the wound, and in this case to
increase the flow of blood. This remarkable compound piercing apparatus
of the drone-fly is of exquisite finish, and must strike the observer with
amazement, while it greatly transcends the work of human mechanism. The
fleshy tongue itself projects some distance from the apparatus described,
and is furnished with setæ or hairs, shorter and fewer in number than those
Page 686
of the house-fly, and while its spiral structure is not so fully developed, its
retractor, muscles, and ligaments are even more so.
The further development of the mouth organs must be looked for in other
members of the insect tribe, when it will be seen many assume a more or
less modified form of structure, that, for example, in Hymenoptera (the bee
and wasp), in which insects the mouth and tongue are divided into lobes
which are used to extract the nectary (as Linnæus termed it) from the plants
on which they feed. The tongue in most species is capable of extension and
contraction.
Fig. 392.
1. Sting of Wasp (Vespa vulgaris), with its muscular attachments and palpi for
cleansing the apparatus; 2. Sting of Bee.
In Fig. 391 the under-surface of the wasp’s tongue is shown, together with
its two pairs of antennæ, and pair of brushes on either side, for brushing off
the gathered pollen and honey from the broad tongue. It is amply provided
with muscular structure. The antennæ, or feelers, are as curious in form as
they are delicate in structure. Those of the male differ from those of the
female.
retractor, muscles, and ligaments are even more so.
The further development of the mouth organs must be looked for in other
members of the insect tribe, when it will be seen many assume a more or
less modified form of structure, that, for example, in Hymenoptera (the bee
and wasp), in which insects the mouth and tongue are divided into lobes
which are used to extract the nectary (as Linnæus termed it) from the plants
on which they feed. The tongue in most species is capable of extension and
contraction.
Fig. 392.
1. Sting of Wasp (Vespa vulgaris), with its muscular attachments and palpi for
cleansing the apparatus; 2. Sting of Bee.
In Fig. 391 the under-surface of the wasp’s tongue is shown, together with
its two pairs of antennæ, and pair of brushes on either side, for brushing off
the gathered pollen and honey from the broad tongue. It is amply provided
with muscular structure. The antennæ, or feelers, are as curious in form as
they are delicate in structure. Those of the male differ from those of the
female.
Page 687
Both the bee and the wasp are armed with an exceedingly venomous sting,
as is well known. This structure takes the form of a well-adapted
mechanical contrivance, and is a weapon of offence as well as of defence.
The sting consists of two barbed needle-points, of a sufficient length to
pierce the flesh to some depth. From the peculiar arrangement of their
serrated edges their immediate withdrawal cannot take place, and it is this
circumstance, with the drop of poison injected into the open wound, that
renders their sting of the most painful and irritating kind. The gland
containing the poison is contained in a minute sac situated at the root of the
piercing apparatus. In Fig. 392 is shown the sting of the wasp and the bee.
Very many insects are provided with instruments for boring into the bark or
solid wood itself. The female Cynip bores into the oak-apple for the
purpose of depositing her egg. The larva, when full grown, eats its way out
of the nut, and drops to the ground, where it attains the form of the perfect
fly (Fig. 393).
There are numbers of species living
exclusively upon the leaves of plants, to
which they do much damage by the
excrescences or galls they form. Each tree
seems to be infested by its own species of
gall-mite, the so-called nail-gall of the lime
being caused by a species named Phytoptus
tibiæ. These galls take the form of a pointed
Fig. 393.—Female Gall-fly and Larva. column, standing erect on the upper side of
the leaf. Galls of much the same structure
occur in the sycamore, maple, elm, and various fruit trees.
The gnat (Culex pipiens) is furnished with a sting curiously constructed
(Fig. 394), and enclosed in a perfectly clothed sheath covered throughout by
scales or feathers. This is folded up when not in use. The mouth is provided
with a complete set of lancets for piercing the flesh; after having inflicted a
severe wound, it injects an acid poison through the proboscis. The scales of
the gnat vary in structure accordingly as these are found on the wing, the
body, or the proboscis. A magnified wing is shown at No. 2, Fig. 394, and a
magnified scale from the proboscis at No. 3. In Fig. 405, Nos. 3 and 5, more
as is well known. This structure takes the form of a well-adapted
mechanical contrivance, and is a weapon of offence as well as of defence.
The sting consists of two barbed needle-points, of a sufficient length to
pierce the flesh to some depth. From the peculiar arrangement of their
serrated edges their immediate withdrawal cannot take place, and it is this
circumstance, with the drop of poison injected into the open wound, that
renders their sting of the most painful and irritating kind. The gland
containing the poison is contained in a minute sac situated at the root of the
piercing apparatus. In Fig. 392 is shown the sting of the wasp and the bee.
Very many insects are provided with instruments for boring into the bark or
solid wood itself. The female Cynip bores into the oak-apple for the
purpose of depositing her egg. The larva, when full grown, eats its way out
of the nut, and drops to the ground, where it attains the form of the perfect
fly (Fig. 393).
There are numbers of species living
exclusively upon the leaves of plants, to
which they do much damage by the
excrescences or galls they form. Each tree
seems to be infested by its own species of
gall-mite, the so-called nail-gall of the lime
being caused by a species named Phytoptus
tibiæ. These galls take the form of a pointed
Fig. 393.—Female Gall-fly and Larva. column, standing erect on the upper side of
the leaf. Galls of much the same structure
occur in the sycamore, maple, elm, and various fruit trees.
The gnat (Culex pipiens) is furnished with a sting curiously constructed
(Fig. 394), and enclosed in a perfectly clothed sheath covered throughout by
scales or feathers. This is folded up when not in use. The mouth is provided
with a complete set of lancets for piercing the flesh; after having inflicted a
severe wound, it injects an acid poison through the proboscis. The scales of
the gnat vary in structure accordingly as these are found on the wing, the
body, or the proboscis. A magnified wing is shown at No. 2, Fig. 394, and a
magnified scale from the proboscis at No. 3. In Fig. 405, Nos. 3 and 5, more
Page 688
highly magnified wing and body scales are given. The proboscis is
protected on either side by antennæ and feelers.
Fig. 394.
1. Head of Culex pipiens, female Gnat, detached from body; 2. Wing, showing
nervature and fringed edges; 3. Scale from Proboscis; 4. Proboscis and Lancets.
The reticulated markings on each side of the head show the proportionate space
occupied by the eyes.
The giant-tailed wasp, Sirax gigas, is furnished with an even more curious
mechanical boring apparatus (Fig. 395) than its congeners. This is a boring
ovipositor, skilfully contrived for piercing the bark of trees, in which the
insect deposits her eggs, and where the larva, when hatched, will find an
ample supply of food to carry it through this stage of existence. The boring
tube, it will be seen, is a perfect muscular structure (c, c, a, and x); in short,
protected on either side by antennæ and feelers.
Fig. 394.
1. Head of Culex pipiens, female Gnat, detached from body; 2. Wing, showing
nervature and fringed edges; 3. Scale from Proboscis; 4. Proboscis and Lancets.
The reticulated markings on each side of the head show the proportionate space
occupied by the eyes.
The giant-tailed wasp, Sirax gigas, is furnished with an even more curious
mechanical boring apparatus (Fig. 395) than its congeners. This is a boring
ovipositor, skilfully contrived for piercing the bark of trees, in which the
insect deposits her eggs, and where the larva, when hatched, will find an
ample supply of food to carry it through this stage of existence. The boring
tube, it will be seen, is a perfect muscular structure (c, c, a, and x); in short,
Page 689
it is an endless form of drill, well known to the mechanic, such as is
employed in fine work for drilling holes. The females are of some size, and
may be surprised and taken in the act of boring through the bark of the pine
tree, for which they have a preference.
There is also a species of the
broad-bodied saw-fly, Lyda
campestris. These bore the
Scotch fir, and deposit their eggs.
The larvæ from these eggs, when
hatched out, feed upon the pine-
needles, first spinning a fine web
to conceal their work of
depredation. A better known saw-
fly, Abraxas grossulariata, plays
havoc among our gooseberry
trees. The female is provided
with a curious mechanical
apparatus as an ovipositor, with
which she cuts into the thicker
under-leaf of the plant. This
penetrating and cutting tool
consists of a double-saw (Fig.
396) of elaborate construction,
which when not in use is kept
concealed in a long narrow case
situated beneath the abdomen. It
Fig. 395.—Boring apparatus of Giant-tailed Wasp is further protected by two horny
(Sirex gigas), × 350. plates. The saws pass out through
a deep groove so arranged that
the saws work side by side backwards and forwards, without a possibility of
running out of the groove. When the cut is made, the four are drawn
together and form a central canal, through which an egg is forced into the
leaf. The cutting edges of the saws are provided with about eighteen or
twenty teeth; these have sharp points of extreme delicacy, and together
make a serrated edge of the exact form given to the finest and best-made
surgical saws of the present day. In the summer-time the proceedings of the
employed in fine work for drilling holes. The females are of some size, and
may be surprised and taken in the act of boring through the bark of the pine
tree, for which they have a preference.
There is also a species of the
broad-bodied saw-fly, Lyda
campestris. These bore the
Scotch fir, and deposit their eggs.
The larvæ from these eggs, when
hatched out, feed upon the pine-
needles, first spinning a fine web
to conceal their work of
depredation. A better known saw-
fly, Abraxas grossulariata, plays
havoc among our gooseberry
trees. The female is provided
with a curious mechanical
apparatus as an ovipositor, with
which she cuts into the thicker
under-leaf of the plant. This
penetrating and cutting tool
consists of a double-saw (Fig.
396) of elaborate construction,
which when not in use is kept
concealed in a long narrow case
situated beneath the abdomen. It
Fig. 395.—Boring apparatus of Giant-tailed Wasp is further protected by two horny
(Sirex gigas), × 350. plates. The saws pass out through
a deep groove so arranged that
the saws work side by side backwards and forwards, without a possibility of
running out of the groove. When the cut is made, the four are drawn
together and form a central canal, through which an egg is forced into the
leaf. The cutting edges of the saws are provided with about eighteen or
twenty teeth; these have sharp points of extreme delicacy, and together
make a serrated edge of the exact form given to the finest and best-made
surgical saws of the present day. In the summer-time the proceedings of the
Page 690
female insect may be witnessed, and the method of using this curious
instrument seen, by the aid of a hand magnifier. These insects are not easily
alarmed when busy at work.
Fig. 396.—Saws of the Gooseberry-fly (Abraxas grossulariata).
Before bringing my remarks on proboscides of insects to a conclusion,
attention must be given to that of the honey bee (Apis mellifica), and its
curious accessories. The mouth of bees exhibits a combination of the
suctorial and the masticatory form of oral apparatus. Thus the labial, or
upper lip, and the mandibles, or large pair of jaws, are well developed,
while the maxillæ, or lesser pair, are elongated to form a tubular organ,
through which, together with the tongue, the flower juices, “honey-dew,”
may be sucked up. The labium, lower lip, is also rather prolonged, and the
palpi, or organs of touch, with which it is endowed form a useful protective
apparatus. The mandibles are employed by bees in the construction of their
abodes, while the suctorial portion of the mouth is devoted to the reception
of nourishment and to prehension. The sting of the bee, already noticed, is
in fact an ovipositor, the female alone being provided with this weapon as
an egg-depositing organ, although better known as an aculeus or sting; but
instrument seen, by the aid of a hand magnifier. These insects are not easily
alarmed when busy at work.
Fig. 396.—Saws of the Gooseberry-fly (Abraxas grossulariata).
Before bringing my remarks on proboscides of insects to a conclusion,
attention must be given to that of the honey bee (Apis mellifica), and its
curious accessories. The mouth of bees exhibits a combination of the
suctorial and the masticatory form of oral apparatus. Thus the labial, or
upper lip, and the mandibles, or large pair of jaws, are well developed,
while the maxillæ, or lesser pair, are elongated to form a tubular organ,
through which, together with the tongue, the flower juices, “honey-dew,”
may be sucked up. The labium, lower lip, is also rather prolonged, and the
palpi, or organs of touch, with which it is endowed form a useful protective
apparatus. The mandibles are employed by bees in the construction of their
abodes, while the suctorial portion of the mouth is devoted to the reception
of nourishment and to prehension. The sting of the bee, already noticed, is
in fact an ovipositor, the female alone being provided with this weapon as
an egg-depositing organ, although better known as an aculeus or sting; but
Page 691
it forms no part of the oral apparatus (as shown in Fig. 397). The proboscis
itself will be seen to be curiously divided; the divisions are elegant and
regular, beset with numerous setæ or hairs. The two horny outside lancets
are spear-shaped and partially set with short hairs; at the base of each is a
hinge articulation; this permits of considerable motion in several directions,
and is much used by the busy insect for forcing open the more internal parts
of flowers, thus facilitating the introduction of the proboscis. The two
shorter feelers are closely connected with the proboscis, and terminate in
three-jointed articulations. The structure of the proboscis is so arranged that
it can be enlarged at the base, and thus made to contain a greater quantity of
the collected honey-dew; at the same time it is in this cavity the nectar
appears to be converted into pure honey. The proboscis tapers off to a little
nipple-like extremity, and at its base is seen two shorter and stronger
mandibles, from between which is protruded a long and narrow lance-like
tongue, the whole being most curiously connected by a series of strong
muscles and ligaments. The basal or first joint of the hind leg in the neuter
or working bee is developed into an enlarged form of pocket, used by the
insect for conveying the pollen of flowers and the propolis to the hive.
Indeed, both the tibia and the first joint of the tarsus are broadened out into
plates, but the two sides of the plates are differently furnished. On one side
is a thick coating of hairs, those on the tarsus taking the form of a brush,
evidently used for brushing out the pollen, as these special developments
are not found on the hind legs of the drones or of the queen.
itself will be seen to be curiously divided; the divisions are elegant and
regular, beset with numerous setæ or hairs. The two horny outside lancets
are spear-shaped and partially set with short hairs; at the base of each is a
hinge articulation; this permits of considerable motion in several directions,
and is much used by the busy insect for forcing open the more internal parts
of flowers, thus facilitating the introduction of the proboscis. The two
shorter feelers are closely connected with the proboscis, and terminate in
three-jointed articulations. The structure of the proboscis is so arranged that
it can be enlarged at the base, and thus made to contain a greater quantity of
the collected honey-dew; at the same time it is in this cavity the nectar
appears to be converted into pure honey. The proboscis tapers off to a little
nipple-like extremity, and at its base is seen two shorter and stronger
mandibles, from between which is protruded a long and narrow lance-like
tongue, the whole being most curiously connected by a series of strong
muscles and ligaments. The basal or first joint of the hind leg in the neuter
or working bee is developed into an enlarged form of pocket, used by the
insect for conveying the pollen of flowers and the propolis to the hive.
Indeed, both the tibia and the first joint of the tarsus are broadened out into
plates, but the two sides of the plates are differently furnished. On one side
is a thick coating of hairs, those on the tarsus taking the form of a brush,
evidently used for brushing out the pollen, as these special developments
are not found on the hind legs of the drones or of the queen.
Page 692
Fig. 397.
1. Honey bee’s tongue; 2. Leg of worker bee. (The small circles show the objects
about the natural size.)
1. Honey bee’s tongue; 2. Leg of worker bee. (The small circles show the objects
about the natural size.)
Page 693
Fig. 398.
1. Foot and leg of Ophion; 2. Foot and leg of Flesh-fly; 3. Foot and leg of Drone-
fly, with pad or sucker appendage.
The wax used in the formation of cells is a secretion that exudes through
certain portions of the body of the bee, since it is found in little pouches
situated on the under part of the body, but it is not brought home ready for
use. The walls of the cells are strengthened when completed by a kind of
varnish, already referred to as the propolis, collected from the buds of
poplar and lime trees, and this is spread over the walls of the cell by that
wonderful pair of broad spatulæ, represented in the drawing.
Many interesting variations will be found in the legs and feet of flies, as
well as in those of other orders of insects (Lepidoptera). One or two typical
forms are represented in Plate VI., and in Fig. 398.
The tarsus, or foot of the fly (Fig. 398), consists of a deeply bifid,
membranous structure, pulvillus; anterior to its attachment to the fifth tarsal
joint, or the upper surface, are seated two claws, or “tarsal ungues”; these
are freely movable in every direction. These ungues differ greatly in their
outline, size, and relative development to the tarsi, and to the bodies of the
insects possessing them, and in their covering; most are naked over their
1. Foot and leg of Ophion; 2. Foot and leg of Flesh-fly; 3. Foot and leg of Drone-
fly, with pad or sucker appendage.
The wax used in the formation of cells is a secretion that exudes through
certain portions of the body of the bee, since it is found in little pouches
situated on the under part of the body, but it is not brought home ready for
use. The walls of the cells are strengthened when completed by a kind of
varnish, already referred to as the propolis, collected from the buds of
poplar and lime trees, and this is spread over the walls of the cell by that
wonderful pair of broad spatulæ, represented in the drawing.
Many interesting variations will be found in the legs and feet of flies, as
well as in those of other orders of insects (Lepidoptera). One or two typical
forms are represented in Plate VI., and in Fig. 398.
The tarsus, or foot of the fly (Fig. 398), consists of a deeply bifid,
membranous structure, pulvillus; anterior to its attachment to the fifth tarsal
joint, or the upper surface, are seated two claws, or “tarsal ungues”; these
are freely movable in every direction. These ungues differ greatly in their
outline, size, and relative development to the tarsi, and to the bodies of the
insects possessing them, and in their covering; most are naked over their
Page 694
entire surface, having however a
hexagonal network at their bases,
which indicates a rudimentary
condition of minute scale-like hairs,
such as are common on some part of
the integument of all insects. Flexor
and extensor muscles are attached to
both ungues and flaps; the flaps are
either corrugated or arranged on the
ridge and furrow plan, in other cases
they are perfectly smooth on their
free surface, while others are covered
with minute scale-like hairs. The
thickness of the divided membrane
Fig. 399.—Sucker on the leg of Water-beetle.
(The dot in the circle represents the object natural on the blow-fly does not exceed the
size.) 1⁄2000th of an inch at the margin; they
somewhat increase in thickness
towards the point of attachment. Projecting from the flap are organs which
have been termed “hairs,” “hair-like appendages,” “trumpet-shaped hairs.”
These are doubtless the immediate agents in holding on to a smooth surface,
as that of glass, and are termed “tenent-hairs,” in allusion to their office.
The under surface of left forefoot of Musca vomitoria is shown with tenent-
hairs (Plate VI., No. 140); a and b are more magnified hairs, a from below,
b from the side. No. 142 is the left forefoot of Amara communis, showing
the under surface and form of tenent appendages, one of which is seen more
magnified at a; No. 143, under surface of left forefoot, Ephydra riparia.
This fly is met with in immense numbers on the surface water in salt
marshes. It does not possess the power of climbing glass; this is explained
by the structure of the tenent-hairs; the central tactile organ is also very
peculiar, the whole acting as a float, one to each foot, to enable the fly to
rest on the surface of the water; a is one of the external hairs, No. 135,
under surface of left forefoot of Cassida viridis (tortoise-beetle), showing
the bifurcate tenent appendages, one of which is given at a more magnified.
These, in ground beetles, are met with only in males, and are used for
sexual purposes. The delicacy of the structure of these hairs in the fly and
the elastic membranous expansion of the foot are marvellous. When the fly
hexagonal network at their bases,
which indicates a rudimentary
condition of minute scale-like hairs,
such as are common on some part of
the integument of all insects. Flexor
and extensor muscles are attached to
both ungues and flaps; the flaps are
either corrugated or arranged on the
ridge and furrow plan, in other cases
they are perfectly smooth on their
free surface, while others are covered
with minute scale-like hairs. The
thickness of the divided membrane
Fig. 399.—Sucker on the leg of Water-beetle.
(The dot in the circle represents the object natural on the blow-fly does not exceed the
size.) 1⁄2000th of an inch at the margin; they
somewhat increase in thickness
towards the point of attachment. Projecting from the flap are organs which
have been termed “hairs,” “hair-like appendages,” “trumpet-shaped hairs.”
These are doubtless the immediate agents in holding on to a smooth surface,
as that of glass, and are termed “tenent-hairs,” in allusion to their office.
The under surface of left forefoot of Musca vomitoria is shown with tenent-
hairs (Plate VI., No. 140); a and b are more magnified hairs, a from below,
b from the side. No. 142 is the left forefoot of Amara communis, showing
the under surface and form of tenent appendages, one of which is seen more
magnified at a; No. 143, under surface of left forefoot, Ephydra riparia.
This fly is met with in immense numbers on the surface water in salt
marshes. It does not possess the power of climbing glass; this is explained
by the structure of the tenent-hairs; the central tactile organ is also very
peculiar, the whole acting as a float, one to each foot, to enable the fly to
rest on the surface of the water; a is one of the external hairs, No. 135,
under surface of left forefoot of Cassida viridis (tortoise-beetle), showing
the bifurcate tenent appendages, one of which is given at a more magnified.
These, in ground beetles, are met with only in males, and are used for
sexual purposes. The delicacy of the structure of these hairs in the fly and
the elastic membranous expansion of the foot are marvellous. When the fly
Page 695
is climbing, a minute quantity of some glutinous fluid is exuded, so that the
tubular nature of the tenent-hairs hardly admits of a doubt.
“At the root of the pulvillus, or its under surface, is a process, which in
some instances is short and thick, in others long and curved, and tapering to
its extremity (Scatophaga), setose (Empis), plumose (Hippoboscidæ), or, in
one remarkable example (Ephydra), closely resembling in its appearance
the very rudimentary pulvillus with which it is associated. Just at the base
of the fifth tarsal joint, on its under surface, there is present, in Eristalis, a
pair of short, very slightly curved hairs, which point almost directly
downwards.”82
Tenent-hairs are usually present in some modification or other. It is really
difficult to name a beetle which has not some form of them; the only one I
yet know that seems to me really to possess nothing of the kind is a species
of Helops, living on sandy heaths. I suppose the dense cushion of hairs on
the tarsi to be for the protection, simply, of the joints to which they are
attached. I have detected them on the tarsal joints of species of Ephydra,
and on the first basal tarsal joint of the drone of the hive-bee. A very
rudimentary form of tenent-hairs is present on the under surface of some of
the tree-bugs (Pentatomidæ), which have in addition a large, deeply-cleft
organ at the extremity of the tarsus; this appears to be a true sucker.
When walking on a rough surface, the foot represents that of a Coleopterous
insect without any tenent appendages. The ungues are always attached to
the last joint of an insect’s tarsus. They are not attached to the fifth tarsal
joint of a Dipterous insect, neither are they attached to the fifth tarsal joint
of a Hymenopterous insect, but to the terminal sucker, which again, in this
great order, is a sixth tarsal joint, membranous, flexible, elastic in the
highest degree, retractile to almost its fullest extent within the fifth tarsal
joint—a joint modified to an extraordinary degree for special purposes.
In plantula of Lucanus, with its pair of minute claws, the ungues are hairs
modified for special purposes; and they have the structure of true hairs. The
sustentacula of Epeira, the analogous structures on the entire under surface
of the last tarsal joints in Pholcus, the condition of the parts in the hind
limbs of Notonecta, in both its mature and earlier conditions, as well as in
Sarcoptes, Psoroptes, and some other Acari, all may be cited in proof of this
tubular nature of the tenent-hairs hardly admits of a doubt.
“At the root of the pulvillus, or its under surface, is a process, which in
some instances is short and thick, in others long and curved, and tapering to
its extremity (Scatophaga), setose (Empis), plumose (Hippoboscidæ), or, in
one remarkable example (Ephydra), closely resembling in its appearance
the very rudimentary pulvillus with which it is associated. Just at the base
of the fifth tarsal joint, on its under surface, there is present, in Eristalis, a
pair of short, very slightly curved hairs, which point almost directly
downwards.”82
Tenent-hairs are usually present in some modification or other. It is really
difficult to name a beetle which has not some form of them; the only one I
yet know that seems to me really to possess nothing of the kind is a species
of Helops, living on sandy heaths. I suppose the dense cushion of hairs on
the tarsi to be for the protection, simply, of the joints to which they are
attached. I have detected them on the tarsal joints of species of Ephydra,
and on the first basal tarsal joint of the drone of the hive-bee. A very
rudimentary form of tenent-hairs is present on the under surface of some of
the tree-bugs (Pentatomidæ), which have in addition a large, deeply-cleft
organ at the extremity of the tarsus; this appears to be a true sucker.
When walking on a rough surface, the foot represents that of a Coleopterous
insect without any tenent appendages. The ungues are always attached to
the last joint of an insect’s tarsus. They are not attached to the fifth tarsal
joint of a Dipterous insect, neither are they attached to the fifth tarsal joint
of a Hymenopterous insect, but to the terminal sucker, which again, in this
great order, is a sixth tarsal joint, membranous, flexible, elastic in the
highest degree, retractile to almost its fullest extent within the fifth tarsal
joint—a joint modified to an extraordinary degree for special purposes.
In plantula of Lucanus, with its pair of minute claws, the ungues are hairs
modified for special purposes; and they have the structure of true hairs. The
sustentacula of Epeira, the analogous structures on the entire under surface
of the last tarsal joints in Pholcus, the condition of the parts in the hind
limbs of Notonecta, in both its mature and earlier conditions, as well as in
Sarcoptes, Psoroptes, and some other Acari, all may be cited in proof of this
Page 696
fact. The various orders of insects have, for the most part, each their own
type of foot. Thus there is the Coleopterous type, the Hymenopterous type,
the Dipterous type, the Homopterous type, &c.; each so very distinctive,
that in critical instances they will sometimes serve at once to show to which
order an insect should be referred. Thus, amongst all the Diptera, I have as
yet met with but one subdivision which presents an exception to the
structure described. This exception is furnished by the Tipulidæ, which have
the Hymenopterous foot. With hardly an exception, then, I believe the form
of foot described will be found universal among the Diptera.
It may be desirable to add a few words on the best plan of conducting
observations on the feet of insects. Their action should be studied by
placing the insect under the influence of chloroform. It is of advantage to
carefully preserve the parts examined, and for this purpose Deane’s medium
or glycerine jelly suits very well; some of the more delicate preparations,
however, can only be kept unchanged in a solution of chloride of zinc. The
plan of soaking in caustic potash, crushing, washing, putting into spirits of
wine and then into turpentine, and lastly into Canada balsam, is perfectly
useless, excepting in rare instances where points connected with the
structure of the integument have to be made out. Of course, the parts should
be viewed from above, from below, and in profile, in order to gain exact
ideas of their relations. The binocular microscope diminishes the difficulties
which formerly had to be encountered, as by its aid many parts may be
clearly viewed without preparation of any kind.
type of foot. Thus there is the Coleopterous type, the Hymenopterous type,
the Dipterous type, the Homopterous type, &c.; each so very distinctive,
that in critical instances they will sometimes serve at once to show to which
order an insect should be referred. Thus, amongst all the Diptera, I have as
yet met with but one subdivision which presents an exception to the
structure described. This exception is furnished by the Tipulidæ, which have
the Hymenopterous foot. With hardly an exception, then, I believe the form
of foot described will be found universal among the Diptera.
It may be desirable to add a few words on the best plan of conducting
observations on the feet of insects. Their action should be studied by
placing the insect under the influence of chloroform. It is of advantage to
carefully preserve the parts examined, and for this purpose Deane’s medium
or glycerine jelly suits very well; some of the more delicate preparations,
however, can only be kept unchanged in a solution of chloride of zinc. The
plan of soaking in caustic potash, crushing, washing, putting into spirits of
wine and then into turpentine, and lastly into Canada balsam, is perfectly
useless, excepting in rare instances where points connected with the
structure of the integument have to be made out. Of course, the parts should
be viewed from above, from below, and in profile, in order to gain exact
ideas of their relations. The binocular microscope diminishes the difficulties
which formerly had to be encountered, as by its aid many parts may be
clearly viewed without preparation of any kind.
Page 697
Fig. 400.
1. Antenna of the Silkworm-moth; 2. Tongue of Butterfly; 3. A portion of tongue
highly magnified, showing its muscular fibre; 4. Tracheæ of silkworm; 5. Foot of
silkworm. (The small circles enclose each object somewhat near the natural size.)
Moths and butterflies supply the microscopist with some of the most
beautiful objects for examination. What can be more wonderful in its
adaptation than the antenna of the moth (represented in Fig. 400, No. 1),
with a thin, finger-like extremity almost supplying the insect with a perfect
and useful hand, moved throughout its extent by a muscular apparatus of
the most exquisite construction. The tongue of butterfly (No. 2) is evidently
made for the purpose of dipping into the interior of flowers and extracting
the juices; this act is assisted by a series of fine muscles. An enlarged view
of a portion is given at No. 3; see Plate VI., Nos. 132 and 133, antennæ of
Vapour Moth.
1. Antenna of the Silkworm-moth; 2. Tongue of Butterfly; 3. A portion of tongue
highly magnified, showing its muscular fibre; 4. Tracheæ of silkworm; 5. Foot of
silkworm. (The small circles enclose each object somewhat near the natural size.)
Moths and butterflies supply the microscopist with some of the most
beautiful objects for examination. What can be more wonderful in its
adaptation than the antenna of the moth (represented in Fig. 400, No. 1),
with a thin, finger-like extremity almost supplying the insect with a perfect
and useful hand, moved throughout its extent by a muscular apparatus of
the most exquisite construction. The tongue of butterfly (No. 2) is evidently
made for the purpose of dipping into the interior of flowers and extracting
the juices; this act is assisted by a series of fine muscles. An enlarged view
of a portion is given at No. 3; see Plate VI., Nos. 132 and 133, antennæ of
Vapour Moth.
Page 698
Fig. 401.—Breathing aperture or spiracle of Fig. 402.—Magnified portions of the trachea
silkworm. (In the circle it is shown of the Hydrophilus, showing spiral
about the natural size.) tubes.
The inconceivably delicate structure of the maxillæ or tongues (for there are
two) of the butterfly, rolled up like the trunk of an elephant, and capable,
like it, of every variety of movement, has been carefully examined and
described by Mr. Newport. “Each maxilla is convex on its outer surface, but
concave on its inner; so that when the two are united they form a tube,
haustellium, by their union, through which fluids may be drawn into the
mouth. The inner or concave surface, which forms the tube, is lined with a
very smooth membrane, and extends throughout the whole length of the
organ; while that of each maxilla is hollow in its interior, apparently
forming a tube ‘in itself,’ but this is not so; the mistake has arisen from the
existence of large tracheæ, or breathing tubes, in the interior of the
proboscis. In some species the extremity of the haustellium is studded
externally with a number of minute papillæ, or fringes—as in Vanessa
atalanta—in which they become small elongated barrel-shaped bodies,
terminated by smaller papillæ at their extremities. On alighting on a flower,
the insect makes a powerful expiratory effort, by which the air is expelled
from the interior air-tubes, and from those with which they are connected in
the head and body; and at the moment of applying its proboscis to the food,
it makes an inspiratory effort, by which the central canal in the proboscis is
silkworm. (In the circle it is shown of the Hydrophilus, showing spiral
about the natural size.) tubes.
The inconceivably delicate structure of the maxillæ or tongues (for there are
two) of the butterfly, rolled up like the trunk of an elephant, and capable,
like it, of every variety of movement, has been carefully examined and
described by Mr. Newport. “Each maxilla is convex on its outer surface, but
concave on its inner; so that when the two are united they form a tube,
haustellium, by their union, through which fluids may be drawn into the
mouth. The inner or concave surface, which forms the tube, is lined with a
very smooth membrane, and extends throughout the whole length of the
organ; while that of each maxilla is hollow in its interior, apparently
forming a tube ‘in itself,’ but this is not so; the mistake has arisen from the
existence of large tracheæ, or breathing tubes, in the interior of the
proboscis. In some species the extremity of the haustellium is studded
externally with a number of minute papillæ, or fringes—as in Vanessa
atalanta—in which they become small elongated barrel-shaped bodies,
terminated by smaller papillæ at their extremities. On alighting on a flower,
the insect makes a powerful expiratory effort, by which the air is expelled
from the interior air-tubes, and from those with which they are connected in
the head and body; and at the moment of applying its proboscis to the food,
it makes an inspiratory effort, by which the central canal in the proboscis is
Page 699
dilated, and the food ascends it at the same instant to supply the vacuum
produced; and thus it passes into the mouth and stomach, the constant
ascent of the fluid being assisted by the action of the muscles of the
proboscis, which continues during the whole time that the insect is feeding.
By this combined agency of the acts of respiration and the muscles of the
proboscis we are also enabled to understand the manner in which the
humming-bird sphynx extracts in an instant the honey from a flower while
hovering over it, without alighting; and which it certainly would be unable
to do were the ascent of the fluid entirely dependent upon the action of the
muscles of the organ.”
The trachæal or respiratory system of insects varies, or rather is found to
exist in modified forms to suit their varied conditions of life. While in the
larval stage the breathing apertures are seen to recur at intervals on each
side of the abdomen (as that of the silkworm, Fig. 401), thus ensuring a
continuous supply of air to the circulating fluids throughout the whole body.
These spiracles are usually nine or ten in number, and consist of a
membranous ring of an oval form. The air-tubes are exquisitely composed
of two thin membranes, between which a delicate elastic thread or spiral
fibre is interposed, forming a cylindrical opening and keeping the tube in a
distended condition, thus mechanically preserving the sides from collapse
or pressure in their passage through the air, which otherwise might occasion
suffocation. Fig. 402 represents the double spiral arrangement of a portion
of a trachea of Hydrophilus, which ensures both elasticity and strength.
There are other points of interest confined to the water-beetle tribe, among
the more striking of which is the foreleg of the Dytiscus marginalis. Here
the first three joints of the tarsus are expanded into a broad surface, and
fringed throughout with curved hairs. From the surface of these spring a
number of short hairs, with cup-like discs at their extremities, one of which
is seen highly magnified in Plate VI., No. 142. These are so cup-like in
form that they have been hitherto described as “suckers,” but it is believed
they are simply a special apparatus for the development of the hairs seen on
the leg and foot of the beetle. Another curious example occurs in the
Gyrinus, or whirligig-beetle. The front pair of legs are of the ordinary kind,
but the under pair are furnished with expanding paddles. The trochanter,
femur, and tibia, are flat plates of a triangular shape, pointed at their outer
produced; and thus it passes into the mouth and stomach, the constant
ascent of the fluid being assisted by the action of the muscles of the
proboscis, which continues during the whole time that the insect is feeding.
By this combined agency of the acts of respiration and the muscles of the
proboscis we are also enabled to understand the manner in which the
humming-bird sphynx extracts in an instant the honey from a flower while
hovering over it, without alighting; and which it certainly would be unable
to do were the ascent of the fluid entirely dependent upon the action of the
muscles of the organ.”
The trachæal or respiratory system of insects varies, or rather is found to
exist in modified forms to suit their varied conditions of life. While in the
larval stage the breathing apertures are seen to recur at intervals on each
side of the abdomen (as that of the silkworm, Fig. 401), thus ensuring a
continuous supply of air to the circulating fluids throughout the whole body.
These spiracles are usually nine or ten in number, and consist of a
membranous ring of an oval form. The air-tubes are exquisitely composed
of two thin membranes, between which a delicate elastic thread or spiral
fibre is interposed, forming a cylindrical opening and keeping the tube in a
distended condition, thus mechanically preserving the sides from collapse
or pressure in their passage through the air, which otherwise might occasion
suffocation. Fig. 402 represents the double spiral arrangement of a portion
of a trachea of Hydrophilus, which ensures both elasticity and strength.
There are other points of interest confined to the water-beetle tribe, among
the more striking of which is the foreleg of the Dytiscus marginalis. Here
the first three joints of the tarsus are expanded into a broad surface, and
fringed throughout with curved hairs. From the surface of these spring a
number of short hairs, with cup-like discs at their extremities, one of which
is seen highly magnified in Plate VI., No. 142. These are so cup-like in
form that they have been hitherto described as “suckers,” but it is believed
they are simply a special apparatus for the development of the hairs seen on
the leg and foot of the beetle. Another curious example occurs in the
Gyrinus, or whirligig-beetle. The front pair of legs are of the ordinary kind,
but the under pair are furnished with expanding paddles. The trochanter,
femur, and tibia, are flat plates of a triangular shape, pointed at their outer
Page 700
angles, from which the apex springs. But the tarsus is jointed on the inner
angle of the furthermost end of the tibia, and each of its four joints expands
into a flat paddle blade. In the accompanying Fig. 403 one paddle is seen
expanded, the other closed.
Fig. 403.
1. Leg of Gyrinus, Whirligig, paddle shown expanded. 2. Paddle closed up.
These paddles are adapted with much precision to ensure the most effectual
application of the propelling power; as the beetle strikes out in the act of
swimming, the membranous expansion described enables it to move about
with great rapidity; upon the legs being drawn back towards the body, the
membrane closes up, and thus offers no resistance to the water. The eyes are
not the least curious part of the merry little beetle: the upper section is fitted
for seeing in the air, and is adapted to the upper or superior part of the head;
the lower portion, for seeing under the water, being placed at a lower angle,
a thin division only separating the two.
angle of the furthermost end of the tibia, and each of its four joints expands
into a flat paddle blade. In the accompanying Fig. 403 one paddle is seen
expanded, the other closed.
Fig. 403.
1. Leg of Gyrinus, Whirligig, paddle shown expanded. 2. Paddle closed up.
These paddles are adapted with much precision to ensure the most effectual
application of the propelling power; as the beetle strikes out in the act of
swimming, the membranous expansion described enables it to move about
with great rapidity; upon the legs being drawn back towards the body, the
membrane closes up, and thus offers no resistance to the water. The eyes are
not the least curious part of the merry little beetle: the upper section is fitted
for seeing in the air, and is adapted to the upper or superior part of the head;
the lower portion, for seeing under the water, being placed at a lower angle,
a thin division only separating the two.
Page 701
Fig. 404.—Scales from Butterflies’ and Moths’ wings, magnified 200 diameters.
1. Scale of Morpho menelaus; 2. Large scale of Polyommatus argiolus, azure blue;
3. Hipparchia janira argiolus; 4. Pontia brassica; 5. Podura plumbea; 6. Small
scale of azure blue.
Wings of Insects.—These exhibit variety of form and structure, as well as of
beauty of colouring. At an early period the orders of insects were mainly
founded upon these interesting appendages. The Orthoptera were the
straight wings; the Neuroptera the nerved; the Trichoptera the hairy wings;
the Coleoptera the cased or sheathed wings; the Diptera the two wings; the
Hymenoptera the married wings; and the Lepidoptera the scaled wings. A
number of wings are small and membranous, and may be mounted dry for
examination under the microscope. Others are better seen mounted in
benzol-balsam. The elytra, iridescent wing cases of the diamond, and other
beetles, as well as the wings of the more highly coloured butterflies, make
pretty objects mounted dry for opaque illumination by the Lieberkühn or
reflector. The thicker horny cases of other members of the beetle tribe
require long soaking, as described in a former chapter.
1. Scale of Morpho menelaus; 2. Large scale of Polyommatus argiolus, azure blue;
3. Hipparchia janira argiolus; 4. Pontia brassica; 5. Podura plumbea; 6. Small
scale of azure blue.
Wings of Insects.—These exhibit variety of form and structure, as well as of
beauty of colouring. At an early period the orders of insects were mainly
founded upon these interesting appendages. The Orthoptera were the
straight wings; the Neuroptera the nerved; the Trichoptera the hairy wings;
the Coleoptera the cased or sheathed wings; the Diptera the two wings; the
Hymenoptera the married wings; and the Lepidoptera the scaled wings. A
number of wings are small and membranous, and may be mounted dry for
examination under the microscope. Others are better seen mounted in
benzol-balsam. The elytra, iridescent wing cases of the diamond, and other
beetles, as well as the wings of the more highly coloured butterflies, make
pretty objects mounted dry for opaque illumination by the Lieberkühn or
reflector. The thicker horny cases of other members of the beetle tribe
require long soaking, as described in a former chapter.
Page 702
The wings of moths and butterflies are covered with scales or feathers,
carefully overlapping each other, as tiles are made to cover the tops of
houses. The iridescent variety of colouring on insects’ wings arises from the
peculiar wavy arrangement of the scales. Figs. 404 and 405 are magnified
representations of a few of them. No. 1, a scale of the Morpho menelaus,
taken from the side of the wing, is of a pale-blue colour; it measures about
1⁄120th of an inch in length, and exhibits a series of longitudinal striæ or
lines, between which are disposed cross-lines or other striæ, giving it very
much an appearance of brick-work (better seen in Fig. 405, No. 1).
Fig. 405.—Portions of Scales, magnified 500 diameters.
1. Portion of scale of Morpho menelaus; 2. Portion of large scale of Podura
plumbea; 3. Scale from the wing of Gnat, its two layers being represented; 4.
Portion of a large scale of Lepisma Saccharina; 5. Body scale of Gnat, magnified
650 diameters.
Polyommatus argiolus, azure-blue (Fig. 404, Nos. 2 and 6), are large and
small scales taken from the under-side of the wing of this beautiful blue
butterfly; the small scale is covered with a series of spots, and exhibits both
carefully overlapping each other, as tiles are made to cover the tops of
houses. The iridescent variety of colouring on insects’ wings arises from the
peculiar wavy arrangement of the scales. Figs. 404 and 405 are magnified
representations of a few of them. No. 1, a scale of the Morpho menelaus,
taken from the side of the wing, is of a pale-blue colour; it measures about
1⁄120th of an inch in length, and exhibits a series of longitudinal striæ or
lines, between which are disposed cross-lines or other striæ, giving it very
much an appearance of brick-work (better seen in Fig. 405, No. 1).
Fig. 405.—Portions of Scales, magnified 500 diameters.
1. Portion of scale of Morpho menelaus; 2. Portion of large scale of Podura
plumbea; 3. Scale from the wing of Gnat, its two layers being represented; 4.
Portion of a large scale of Lepisma Saccharina; 5. Body scale of Gnat, magnified
650 diameters.
Polyommatus argiolus, azure-blue (Fig. 404, Nos. 2 and 6), are large and
small scales taken from the under-side of the wing of this beautiful blue
butterfly; the small scale is covered with a series of spots, and exhibits both
Page 703
longitudinal and transverse striæ, these should be clearly defined, and the
spots separated by a quarter-inch object-glass. No. 3, Hipparchia janira, is a
scale from the meadow-brown butterfly: on this brown spots, having an
irregular shape with longitudinal striæ, are seen. No. 4, Pontia brassica,
cabbage butterfly, was at one time taken to be an excellent criterion of the
penetration and definition of an object glass. It is seen to have a free
extremity or brush-like appendage. With a fairly good power, the
longitudinal markings appear like rows of small beads. Chevalier selected
for his test object the scale of the Pontia brassica. Mohl and Schacht
extolled Hipparchia janira as a good test of penetration in an objective of
moderate angular aperture. Amici’s test object is Navicula rhomboides, the
display of the lines forming the test.
The Tinea vestianella, clothes-moth,
is furnished with unique scales.
Small and destructive as this moth is,
it suffers much from a parasitic mite,
and from which it is unable to free
itself.
The Podura scale (Fig. 405), with its
delicate transparent membrane and
curiously inserted “notes of
admiration,” as they were called, was
long believed to be an excellent test
object for the highest powers of the Fig. 406.—Podura villosa, male and female,
highly magnified.
microscope, but I believe it is no
longer regarded in that light: indeed, most insect scales have declined in the
value and estimation of the skilled microscopist. This is in part due to the
improvements made in the objective. The high-angled glasses have cleared
up obscure points in the structural characters of the minuter forms of life,
and the scales of insects are no longer found to be difficult test objects for
the modern objective of a Zeiss or a Powell to resolve. Nevertheless, the
scale of the Podura belonging to the order Thysanura, a curious little insect
commonly known by the name of springtail, usually found living in most
obscure places, and too small to attract attention, is not likely to be entirely
thrust aside. The springtails (Collembola) are furnished on the under-side of
spots separated by a quarter-inch object-glass. No. 3, Hipparchia janira, is a
scale from the meadow-brown butterfly: on this brown spots, having an
irregular shape with longitudinal striæ, are seen. No. 4, Pontia brassica,
cabbage butterfly, was at one time taken to be an excellent criterion of the
penetration and definition of an object glass. It is seen to have a free
extremity or brush-like appendage. With a fairly good power, the
longitudinal markings appear like rows of small beads. Chevalier selected
for his test object the scale of the Pontia brassica. Mohl and Schacht
extolled Hipparchia janira as a good test of penetration in an objective of
moderate angular aperture. Amici’s test object is Navicula rhomboides, the
display of the lines forming the test.
The Tinea vestianella, clothes-moth,
is furnished with unique scales.
Small and destructive as this moth is,
it suffers much from a parasitic mite,
and from which it is unable to free
itself.
The Podura scale (Fig. 405), with its
delicate transparent membrane and
curiously inserted “notes of
admiration,” as they were called, was
long believed to be an excellent test
object for the highest powers of the Fig. 406.—Podura villosa, male and female,
highly magnified.
microscope, but I believe it is no
longer regarded in that light: indeed, most insect scales have declined in the
value and estimation of the skilled microscopist. This is in part due to the
improvements made in the objective. The high-angled glasses have cleared
up obscure points in the structural characters of the minuter forms of life,
and the scales of insects are no longer found to be difficult test objects for
the modern objective of a Zeiss or a Powell to resolve. Nevertheless, the
scale of the Podura belonging to the order Thysanura, a curious little insect
commonly known by the name of springtail, usually found living in most
obscure places, and too small to attract attention, is not likely to be entirely
thrust aside. The springtails (Collembola) are furnished on the under-side of
Page 704
the first abdominal segment with a curious tube or sucker, from the orifice
of which glandular process a secreted viscid matter is protruded; they are
remarkable also from the fact that in most of them no trace of a tracheal
system has yet been discovered. The eyes when present are in the form of
simple or grouped ocelli, the antennæ number six joints, and the abdomen
has but six segments, often only three. The forked tail is a curious process
turned forward and attached to one of the tender segments and held in
position under the body; when released it springs back and bounds up to a
very considerable height. Fig. 406 represents Podura villosa. There are
several species, one of which (P. aquatica) is found floating in patches on
pools of water on bright summer days.
Lepisma saccharina belongs to the same genus as Podura. This minute
springtail derives its name from having been discovered in old sugar-casks.
It has a spindle-shaped body covered with silvery scales, long used as test
objects. The sides of the abdomen are furnished with a series of appendages
with long bristle-like setæ, or hairs, at their extremities. The head is
concealed under a prothorax, the antennæ are long, and the maxillary palpi
are either five or seven-jointed, and very conspicuous, to enable them to cut
the dry wood on which they principally feed. The scales must be mounted
under thin cover-glasses; oblique illumination shows up some portions to
advantage, while central light from an achromatic condenser and a wide-
angled objective renders their markings more distinct. Portion of a scale
more highly magnified is shown in Fig. 405.
Eggs of Insects (Plate VI., Nos. 124-139).—In form, colour, and variety of
design, the eggs of insects are more surprisingly varied than those of the
feathered tribes; but as from extreme smallness they escape observation, an
acquaintance with their structure is not so familiar as it might be. Although
the eggs of the bird tribe differ much in their external characteristics, they
closely resemble each other while yet a part of the ovarian ova, and prior to
their detachment from the ovary. At one period of their formation all eggs
consist of three similar parts:—1st. The internal nucleated cell, or germinal
vesicle, with its macula; 2nd. The vitellus, or yolk-substance; and 3rd. The
vesicular envelope, or vitelline membrane. The germinal vesicle is the first
produced, then the yolk substance, which gradually envelops it, and the
vitelline membrane, the latest formed, incloses the whole. The chemical
of which glandular process a secreted viscid matter is protruded; they are
remarkable also from the fact that in most of them no trace of a tracheal
system has yet been discovered. The eyes when present are in the form of
simple or grouped ocelli, the antennæ number six joints, and the abdomen
has but six segments, often only three. The forked tail is a curious process
turned forward and attached to one of the tender segments and held in
position under the body; when released it springs back and bounds up to a
very considerable height. Fig. 406 represents Podura villosa. There are
several species, one of which (P. aquatica) is found floating in patches on
pools of water on bright summer days.
Lepisma saccharina belongs to the same genus as Podura. This minute
springtail derives its name from having been discovered in old sugar-casks.
It has a spindle-shaped body covered with silvery scales, long used as test
objects. The sides of the abdomen are furnished with a series of appendages
with long bristle-like setæ, or hairs, at their extremities. The head is
concealed under a prothorax, the antennæ are long, and the maxillary palpi
are either five or seven-jointed, and very conspicuous, to enable them to cut
the dry wood on which they principally feed. The scales must be mounted
under thin cover-glasses; oblique illumination shows up some portions to
advantage, while central light from an achromatic condenser and a wide-
angled objective renders their markings more distinct. Portion of a scale
more highly magnified is shown in Fig. 405.
Eggs of Insects (Plate VI., Nos. 124-139).—In form, colour, and variety of
design, the eggs of insects are more surprisingly varied than those of the
feathered tribes; but as from extreme smallness they escape observation, an
acquaintance with their structure is not so familiar as it might be. Although
the eggs of the bird tribe differ much in their external characteristics, they
closely resemble each other while yet a part of the ovarian ova, and prior to
their detachment from the ovary. At one period of their formation all eggs
consist of three similar parts:—1st. The internal nucleated cell, or germinal
vesicle, with its macula; 2nd. The vitellus, or yolk-substance; and 3rd. The
vesicular envelope, or vitelline membrane. The germinal vesicle is the first
produced, then the yolk substance, which gradually envelops it, and the
vitelline membrane, the latest formed, incloses the whole. The chemical
Page 705
constituents of the egg are the same in all cases, albumen, fatty matters, and
a proportion of a substance precipitable by water. The production of the
chorion, or shell membrane, does not take place till the ovum has attained
nearly its full size, and it then appears to proceed, in part at least, from the
consolidation over the whole surface of one or more layers of an
albuminous fluid secreted from the wall of the oviduct.
The embryo cell is so directly connected with the germinal vesicle that at a
certain period it disappears altogether, and is absorbed into the germinal
yolk, or rather becomes the nucleus of the embryo, when a greater degree of
compactness is observed in the yolk, and all that remains of the germinal
vesicle is one or more highly refracting fat globules and albuminoid bodies.
Towards the end of the period of incubation, the head of the young
caterpillar is said to lie towards the dot or opening in the lid, termed the
micropyle,83 from its resemblance to a small gate, or opening through which
the larva emerges forth as a butterfly.
The germinal vesicle is comparatively large and well-marked while the egg
is yet in the ova-sac. By preparing sections after Dr. Halifax’s method,84 we
find that the germinal vesicle in the bee’s egg is not situated immediately
near or even below the so-called micropyle, but rather more to the side of
the egg; just in the position which the head of the embryo is subsequently
found to occupy at maturity.
The egg membrane, or envelope, of all the Lepidoptera is composed of
three separate and distinct layers: an external slightly raised coat, tough and
hard in its character, a middle one of united cells, and a fine transparent
vitelline lining membrane, perfectly smooth and homogeneous in structure,
imparting solidity, and giving a fine iridescent hue to the surface. The
germinal vesicle is of a proportionately large size for the egg, and its
macula is at first single, then multiple. In the egg of the silkworm the outer
membrane is comprised of an inner reticulated membrane of non-nucleated
cells, in the outer layer the cells are arranged in an irregular circular form,
also non-nucleated, with minute interstitial setæ or hairs projecting outward.
The outer surface of the egg-shell of Coccus Persicæ is covered by minute
rings, of which the ends somewhat overlap. These rings are thought to be
identical in their character with the whitish substance which exudes through
a proportion of a substance precipitable by water. The production of the
chorion, or shell membrane, does not take place till the ovum has attained
nearly its full size, and it then appears to proceed, in part at least, from the
consolidation over the whole surface of one or more layers of an
albuminous fluid secreted from the wall of the oviduct.
The embryo cell is so directly connected with the germinal vesicle that at a
certain period it disappears altogether, and is absorbed into the germinal
yolk, or rather becomes the nucleus of the embryo, when a greater degree of
compactness is observed in the yolk, and all that remains of the germinal
vesicle is one or more highly refracting fat globules and albuminoid bodies.
Towards the end of the period of incubation, the head of the young
caterpillar is said to lie towards the dot or opening in the lid, termed the
micropyle,83 from its resemblance to a small gate, or opening through which
the larva emerges forth as a butterfly.
The germinal vesicle is comparatively large and well-marked while the egg
is yet in the ova-sac. By preparing sections after Dr. Halifax’s method,84 we
find that the germinal vesicle in the bee’s egg is not situated immediately
near or even below the so-called micropyle, but rather more to the side of
the egg; just in the position which the head of the embryo is subsequently
found to occupy at maturity.
The egg membrane, or envelope, of all the Lepidoptera is composed of
three separate and distinct layers: an external slightly raised coat, tough and
hard in its character, a middle one of united cells, and a fine transparent
vitelline lining membrane, perfectly smooth and homogeneous in structure,
imparting solidity, and giving a fine iridescent hue to the surface. The
germinal vesicle is of a proportionately large size for the egg, and its
macula is at first single, then multiple. In the egg of the silkworm the outer
membrane is comprised of an inner reticulated membrane of non-nucleated
cells, in the outer layer the cells are arranged in an irregular circular form,
also non-nucleated, with minute interstitial setæ or hairs projecting outward.
The outer surface of the egg-shell of Coccus Persicæ is covered by minute
rings, of which the ends somewhat overlap. These rings are thought to be
identical in their character with the whitish substance which exudes through
Page 706
pores on the under-side of the body; it is more than probable that a
succession of layers of rings fully accounts for the beautiful prismatic hues
they present viewed as opaque objects under the microscope, and
illuminated by Lieberkühn or side-condenser. This white substance, it
should be observed, forms a part of the intimate structure of the egg-shell,
and is in nowise affected by methylated spirit or dilute acids. Sir John
Lubbock85 states that in the greenish eggs of Phryganea, “the colour is due
to the yolk-globules themselves. In Coccus, however, this is not so; the
yolk-globules are slightly yellow, and the green hue of the egg is owing to
the green granules, which are minute oil globules. When, however, the egg
arrives at maturity, and the upper chamber has been removed by absorption,
these green granules will be found to be replaced by dark-green globules,
regular in size, and about 1⁄8000th of an inch in diameter, and which appear to
be in no way the same in the yolk of Phryganea eggs.” Another curious fact
has been noticed, which partially bears on the question of colour: the
production of parasite bodies within the eggs of some insects. In the
Coccus, for instance, parasitic cells of a green colour occur, “shaped like a
string of sausages, in length about the 1⁄2000th of an inch by about the 1⁄7000th
in breadth.”
The eggs of moths and butterflies present many varying tints of colour; in
speaking of this quality I do not restrict the term solely to those prismatic
changes to which allusion has been made, and which are liable to constant
mutations according to the accident of the rays of light thrown upon them;
but I more particularly refer to the several natural transitions of colour, the
prevailing tints of which are yellow, white, grey, and a light-brown. In some
eggs the yellow, white, and grey are delicately blended, and, when viewed
with a magnifying power of about fifty diameters, and by the aid of the
side-reflector (parabolic-reflector), exhibit many beautiful combinations.
The more delicate opalescent, or rather iridescent, tints appear on the eggs
of insects, while those of the feathered tribes furnish no like example. The
egg of the mottled umber moth, Erannis defoliaria (Plate VI., No. 137), is
in every way very beautiful. It is in shape ovoid, with regular hexagonal
reticulations, each corner being studded with a knob or button; the space
within the hexagon is finely punctated, and the play of colours is exquisitely
delicate. In this egg no micropyle can be seen. The egg of the thorn moth,
Ennomos erosaria (Plate VI., No. 138), is of an elongated brick-looking
succession of layers of rings fully accounts for the beautiful prismatic hues
they present viewed as opaque objects under the microscope, and
illuminated by Lieberkühn or side-condenser. This white substance, it
should be observed, forms a part of the intimate structure of the egg-shell,
and is in nowise affected by methylated spirit or dilute acids. Sir John
Lubbock85 states that in the greenish eggs of Phryganea, “the colour is due
to the yolk-globules themselves. In Coccus, however, this is not so; the
yolk-globules are slightly yellow, and the green hue of the egg is owing to
the green granules, which are minute oil globules. When, however, the egg
arrives at maturity, and the upper chamber has been removed by absorption,
these green granules will be found to be replaced by dark-green globules,
regular in size, and about 1⁄8000th of an inch in diameter, and which appear to
be in no way the same in the yolk of Phryganea eggs.” Another curious fact
has been noticed, which partially bears on the question of colour: the
production of parasite bodies within the eggs of some insects. In the
Coccus, for instance, parasitic cells of a green colour occur, “shaped like a
string of sausages, in length about the 1⁄2000th of an inch by about the 1⁄7000th
in breadth.”
The eggs of moths and butterflies present many varying tints of colour; in
speaking of this quality I do not restrict the term solely to those prismatic
changes to which allusion has been made, and which are liable to constant
mutations according to the accident of the rays of light thrown upon them;
but I more particularly refer to the several natural transitions of colour, the
prevailing tints of which are yellow, white, grey, and a light-brown. In some
eggs the yellow, white, and grey are delicately blended, and, when viewed
with a magnifying power of about fifty diameters, and by the aid of the
side-reflector (parabolic-reflector), exhibit many beautiful combinations.
The more delicate opalescent, or rather iridescent, tints appear on the eggs
of insects, while those of the feathered tribes furnish no like example. The
egg of the mottled umber moth, Erannis defoliaria (Plate VI., No. 137), is
in every way very beautiful. It is in shape ovoid, with regular hexagonal
reticulations, each corner being studded with a knob or button; the space
within the hexagon is finely punctated, and the play of colours is exquisitely
delicate. In this egg no micropyle can be seen. The egg of the thorn moth,
Ennomos erosaria (Plate VI., No. 138), is of an elongated brick-looking
Page 707
form, one end of which is slightly tapered off, while the other, in which the
lid is placed, is flattened and surrounded by a beautifully white-beaded
border, having for its centre a slightly raised reticulated micropyle. The
empty egg-shell gives a fine opalescent play of colours, while that
containing the young worm is of a brownish-yellow.
The egg of the straw-belle moth, Aspillates gilvaria (Plate VI., No. 139), is
delicately tinted, somewhat long and narrow, with sides slightly flattened or
rounded off, and irregularly serrated. The top is convex, and the base a little
indented, in which are seen the lid and micropyle. The young worm,
however, usually makes its way through the upper convex side: the
indentation represented in the drawing shows the place of exit.
An example of those eggs possessing a good deal of natural colour is
presented in that of the common puss-moth, Cerura vinula, a large
spheroidal-shaped egg, having, under the microscope, the appearance of a
fine ripe orange; the micropyle exactly corresponds to the depression left in
this fruit on the removal of the stalk. The surface is finely reticulated, and
the natural colour a deep orange.
The egg of the mottled rustic moth, Caradina morpheus (No. 124), is
subconical, and equally divided throughout by a series of ribs, which
terminate in a well-marked geometrically-formed lid. The egg of the
tortoise-shell butterfly, Vanessa urticæ (No. 125), is ovoid and divided into
segments, the ribs turning in towards the micropyle. The common footman,
Lithosia campanula (No. 126), produces a perfectly globular egg covered
with fine reticulations of a delicate buff colour. The egg of the shark moth,
Cucullia umbratica (No. 127), is subconical in form, with ribs and cross-
bars passing up from a flattened base to the summit, and turning over to
form the lid. No. 136 is the egg of blue argus butterfly, Polyommatus argus.
That of the small emerald moth, Jodis Vernaria (No. 134), is an egg of
singular form and beauty—an oval, flattened on both sides, of silvery
iridescence, and covered throughout with minute reticulations and dots. It is
particularly translucent, so much so that the yellow-brown worm is readily
seen curled up within. The lid or micropyle is not detected until the larva
eats its way out of the shell. It should be noted that the series of eggs in
Plate VII. are somewhat over-coloured, and consequently lose much of their
lid is placed, is flattened and surrounded by a beautifully white-beaded
border, having for its centre a slightly raised reticulated micropyle. The
empty egg-shell gives a fine opalescent play of colours, while that
containing the young worm is of a brownish-yellow.
The egg of the straw-belle moth, Aspillates gilvaria (Plate VI., No. 139), is
delicately tinted, somewhat long and narrow, with sides slightly flattened or
rounded off, and irregularly serrated. The top is convex, and the base a little
indented, in which are seen the lid and micropyle. The young worm,
however, usually makes its way through the upper convex side: the
indentation represented in the drawing shows the place of exit.
An example of those eggs possessing a good deal of natural colour is
presented in that of the common puss-moth, Cerura vinula, a large
spheroidal-shaped egg, having, under the microscope, the appearance of a
fine ripe orange; the micropyle exactly corresponds to the depression left in
this fruit on the removal of the stalk. The surface is finely reticulated, and
the natural colour a deep orange.
The egg of the mottled rustic moth, Caradina morpheus (No. 124), is
subconical, and equally divided throughout by a series of ribs, which
terminate in a well-marked geometrically-formed lid. The egg of the
tortoise-shell butterfly, Vanessa urticæ (No. 125), is ovoid and divided into
segments, the ribs turning in towards the micropyle. The common footman,
Lithosia campanula (No. 126), produces a perfectly globular egg covered
with fine reticulations of a delicate buff colour. The egg of the shark moth,
Cucullia umbratica (No. 127), is subconical in form, with ribs and cross-
bars passing up from a flattened base to the summit, and turning over to
form the lid. No. 136 is the egg of blue argus butterfly, Polyommatus argus.
That of the small emerald moth, Jodis Vernaria (No. 134), is an egg of
singular form and beauty—an oval, flattened on both sides, of silvery
iridescence, and covered throughout with minute reticulations and dots. It is
particularly translucent, so much so that the yellow-brown worm is readily
seen curled up within. The lid or micropyle is not detected until the larva
eats its way out of the shell. It should be noted that the series of eggs in
Plate VII. are somewhat over-coloured, and consequently lose much of their
Page 708
natural transparency. The eggs of flies and parasites also present much
variety in form, colour, and construction. Many of their eggs are provided
with a veritable lid, which opens up with a hinge-like articulation. This lid
is seen in the egg of bot-fly, Plate VI., No. 144, from which the larva is just
escaping; No. 146, egg of Scatophaga; No. 147, egg of parasite of magpie.86
Still more remarkable in the delicate and beautiful forms are some of the
parasities which infest birds in particular: Plate VI., No. 145, the egg of
parasite of pheasant; No. 147, that of the magpie, while that of the peacock
is curiously interesting. In Fig. 407 the larvæ of the horn-bill are seen just
about to emerge from their eggs.
The larvæ of most Hymenoptera are
footless grubs, furnished with a soft
head, and exhibiting but little, if any,
advance upon those of Diptera (Plate
VI., No. 141). In the saw-fly, however,
the larva, instead of being as above
described, a mere footless maggot,
presents the closest resemblance to the
caterpillar of the Lepidoptera; it is
provided with a distinct head, with six
thoracic legs, and in most cases from
twelve to sixteen pro-legs are
appended to the abdominal segments.
One
Fig. 407.—Larvæ of the Hornbill emerging other conspicuous object
from eggs. represented in Plate VI., No. 128, is the
maple Aphis, also known as the leaf-
insect, averaging in size about the one-fiftieth of an inch in length.
Although recognised and described under the name of the leaf-insect,
nothing was known of its origin and history, with the exception of what the
Rev. J. Thornton published in 1852, and to whom we owe its re-discovery
on the leaves of the maple. Subsequently it attracted the attention of the
Dutch naturalist, Van der Hoeven, who regarded it as the larval form of a
species of Aphis, and named it Periphyllus. It has more recently engaged
the attention of Dr. Balbiani and M. Siguoret, whose united investigations
will be found in “Comptes Rendus,” 1867. These observers assigned it
variety in form, colour, and construction. Many of their eggs are provided
with a veritable lid, which opens up with a hinge-like articulation. This lid
is seen in the egg of bot-fly, Plate VI., No. 144, from which the larva is just
escaping; No. 146, egg of Scatophaga; No. 147, egg of parasite of magpie.86
Still more remarkable in the delicate and beautiful forms are some of the
parasities which infest birds in particular: Plate VI., No. 145, the egg of
parasite of pheasant; No. 147, that of the magpie, while that of the peacock
is curiously interesting. In Fig. 407 the larvæ of the horn-bill are seen just
about to emerge from their eggs.
The larvæ of most Hymenoptera are
footless grubs, furnished with a soft
head, and exhibiting but little, if any,
advance upon those of Diptera (Plate
VI., No. 141). In the saw-fly, however,
the larva, instead of being as above
described, a mere footless maggot,
presents the closest resemblance to the
caterpillar of the Lepidoptera; it is
provided with a distinct head, with six
thoracic legs, and in most cases from
twelve to sixteen pro-legs are
appended to the abdominal segments.
One
Fig. 407.—Larvæ of the Hornbill emerging other conspicuous object
from eggs. represented in Plate VI., No. 128, is the
maple Aphis, also known as the leaf-
insect, averaging in size about the one-fiftieth of an inch in length.
Although recognised and described under the name of the leaf-insect,
nothing was known of its origin and history, with the exception of what the
Rev. J. Thornton published in 1852, and to whom we owe its re-discovery
on the leaves of the maple. Subsequently it attracted the attention of the
Dutch naturalist, Van der Hoeven, who regarded it as the larval form of a
species of Aphis, and named it Periphyllus. It has more recently engaged
the attention of Dr. Balbiani and M. Siguoret, whose united investigations
will be found in “Comptes Rendus,” 1867. These observers assigned it
Page 709
definitely to Aphis. A brown species is also met with during a great part of
the year feeding upon the young shoots of the maple. The female produces
two kinds of young, as do all the genus Aphis, one normal the other
abnormal; the first are alone capable of reproducing their species, while the
latter retain their original form, which is not changed throughout their
existence. They increase so slowly in size that it may appear doubtful
whether they eat, the mouth being rudimentary; they undergo no change; do
not acquire wings, and their antennæ always retain the five joints peculiar to
all young Aphides before the first moult. Neither are they all of the same
colour, some being of a bright green, as represented in Plate VI., while
others are of a darker, or brownish-green colour. The brown-green embryos
differ from the adult female only in those characters analogous to all other
species, and this chiefly with regard to the minute hairs, which are long and
simple. In the green embryos, in the place of setæ, the body is surrounded
by transparent lamellæ, oblong in shape. These scales not only cover the
body, but also the anterior portion of the head, the first joint of the antennæ,
and the outer edge of the tibiæ of the first pair of legs. The dorsal surface in
these insects is covered with a mosaic of hexagonal plates, very closely
resembling the plates of the carapace of the tortoise. In this particular my
artist has fallen into a slight error. Another peculiarity is that the body is
much flattened out, and looks so much like a scale on the surface of the leaf
that it requires considerable practice, as well as quickness of sight, to detect
the young maple Aphis. One of the lamellæ is seen highly magnified at c,
and a tenent-hair at b. The antennæ, tapering off towards the apex, are
serrate on both edges, and terminate in a fine lancet (shown at a), with
which it penetrates the leaf of the plant. Beneath the insertions of the
antennæ is a complex form of sucking mouth, and on either side of the head
are two brilliant scarlet-coloured eyes.
Aphides, as is well known, live upon the juices of plants, which they suck,
and when they occur in great numbers cause considerable damage to the
gardener and farmer. Many plants are liable to be attacked by swarms of
these insects, when their leaves curl up, they grow sickly, and their produce
is either greatly reduced or utterly ruined. One striking instance is presented
in the devastation caused by the hop-fly (Aphis humuli).
the year feeding upon the young shoots of the maple. The female produces
two kinds of young, as do all the genus Aphis, one normal the other
abnormal; the first are alone capable of reproducing their species, while the
latter retain their original form, which is not changed throughout their
existence. They increase so slowly in size that it may appear doubtful
whether they eat, the mouth being rudimentary; they undergo no change; do
not acquire wings, and their antennæ always retain the five joints peculiar to
all young Aphides before the first moult. Neither are they all of the same
colour, some being of a bright green, as represented in Plate VI., while
others are of a darker, or brownish-green colour. The brown-green embryos
differ from the adult female only in those characters analogous to all other
species, and this chiefly with regard to the minute hairs, which are long and
simple. In the green embryos, in the place of setæ, the body is surrounded
by transparent lamellæ, oblong in shape. These scales not only cover the
body, but also the anterior portion of the head, the first joint of the antennæ,
and the outer edge of the tibiæ of the first pair of legs. The dorsal surface in
these insects is covered with a mosaic of hexagonal plates, very closely
resembling the plates of the carapace of the tortoise. In this particular my
artist has fallen into a slight error. Another peculiarity is that the body is
much flattened out, and looks so much like a scale on the surface of the leaf
that it requires considerable practice, as well as quickness of sight, to detect
the young maple Aphis. One of the lamellæ is seen highly magnified at c,
and a tenent-hair at b. The antennæ, tapering off towards the apex, are
serrate on both edges, and terminate in a fine lancet (shown at a), with
which it penetrates the leaf of the plant. Beneath the insertions of the
antennæ is a complex form of sucking mouth, and on either side of the head
are two brilliant scarlet-coloured eyes.
Aphides, as is well known, live upon the juices of plants, which they suck,
and when they occur in great numbers cause considerable damage to the
gardener and farmer. Many plants are liable to be attacked by swarms of
these insects, when their leaves curl up, they grow sickly, and their produce
is either greatly reduced or utterly ruined. One striking instance is presented
in the devastation caused by the hop-fly (Aphis humuli).
Page 710
The Aphrophora bifasciata, common
frog-hopper, is a well-known garden
pest. The antennæ of this insect are
placed between the eyes, and the
scutellum is not covered; the eyes,
never more than two in number, are
occasionally wanting. These pests are
Fig. 408.—Aphrophora spumaria, Cuckoo-
spit.
furnished with long hind legs, that
enable them to perform most
a. The frothy substance; b. The pupa. extraordinary leaping feats. The best-
known British species is the cuckoo-
spit, froth-fly (Fig. 408). The names cuckoo-spit and froth-fly both allude to
the peculiar habit of the insect, while in the larva state, of enveloping itself
in a kind of frothy secretion, somewhat resembling saliva.
Arachnidæ.—In this class of insects, spiders, scorpions, and mites are
included, all of which belong to a sub-class of Arthropoda, and are
appropriately placed between the Crustacea on the one hand and the Insecta
on the other. The highest Crustaceans have ten feet, the Arachnidæ eight,
and insects six. The Arachnidæ are wingless, have no antennæ, and breathe
by means of tracheal tubes, or pulmonary sacs, these performing the
function of lungs. As a rule they have several simple eyes, have no proper
metamorphosis, and they are essentially predaceous, the females being
larger than the males. Most of the Arachnidæ live on insects, and may
therefore be regarded in the light of a friend to the florist and gardener.
The Epeira diadema is the best known member of the species; in summer
spiders abound on every shrub, and spin out their wonderful webs from
branch to branch.
frog-hopper, is a well-known garden
pest. The antennæ of this insect are
placed between the eyes, and the
scutellum is not covered; the eyes,
never more than two in number, are
occasionally wanting. These pests are
Fig. 408.—Aphrophora spumaria, Cuckoo-
spit.
furnished with long hind legs, that
enable them to perform most
a. The frothy substance; b. The pupa. extraordinary leaping feats. The best-
known British species is the cuckoo-
spit, froth-fly (Fig. 408). The names cuckoo-spit and froth-fly both allude to
the peculiar habit of the insect, while in the larva state, of enveloping itself
in a kind of frothy secretion, somewhat resembling saliva.
Arachnidæ.—In this class of insects, spiders, scorpions, and mites are
included, all of which belong to a sub-class of Arthropoda, and are
appropriately placed between the Crustacea on the one hand and the Insecta
on the other. The highest Crustaceans have ten feet, the Arachnidæ eight,
and insects six. The Arachnidæ are wingless, have no antennæ, and breathe
by means of tracheal tubes, or pulmonary sacs, these performing the
function of lungs. As a rule they have several simple eyes, have no proper
metamorphosis, and they are essentially predaceous, the females being
larger than the males. Most of the Arachnidæ live on insects, and may
therefore be regarded in the light of a friend to the florist and gardener.
The Epeira diadema is the best known member of the species; in summer
spiders abound on every shrub, and spin out their wonderful webs from
branch to branch.
Page 711
Fig. 409.—A lengthways section through the body of female Epeira diadema.
Explanation of reference.—ey. Eyes; p.g. Poison gland; ht. Heart; in. Intestine,
alimentary canal; l. Liver; r. Rectum or cloaca; dt. and sp. Discharge tubes of
spinnerets; o. Slit, or air opening; ov. Ovipositor; ph. Pharynx; br. Brain; thr.
Throat, or gullet, filled with eggs; un. l. Under lip; m. Mouth; f. Fang, or claw; j.
Jaw. The gills, or breathing apparatus are situated at the air opening, o; and the silk
glands are above this. (Magnified 20 diameters.)
The body, seen in my illustration, Fig. 409, in section, consists of two parts;
the foremost is the cephalothorax, or head, upon which is mounted four
pairs of eyes (two of which are seen in section), while to the thorax is
attached eight jointed well-developed legs terminating in feet, with claws
adapted for climbing and holding on. The other half consists, of the
abdomen, together with spinnerets and glands, which secrete the fluid out of
which the web is spun, and this, although it hardens to some extent on
exposure to the air, retains its viscid nature for the purpose of entangling its
prey. The spinnerets are the most interesting feature in the anatomy of the
Epeira (Figs. 410 and 411).
Explanation of reference.—ey. Eyes; p.g. Poison gland; ht. Heart; in. Intestine,
alimentary canal; l. Liver; r. Rectum or cloaca; dt. and sp. Discharge tubes of
spinnerets; o. Slit, or air opening; ov. Ovipositor; ph. Pharynx; br. Brain; thr.
Throat, or gullet, filled with eggs; un. l. Under lip; m. Mouth; f. Fang, or claw; j.
Jaw. The gills, or breathing apparatus are situated at the air opening, o; and the silk
glands are above this. (Magnified 20 diameters.)
The body, seen in my illustration, Fig. 409, in section, consists of two parts;
the foremost is the cephalothorax, or head, upon which is mounted four
pairs of eyes (two of which are seen in section), while to the thorax is
attached eight jointed well-developed legs terminating in feet, with claws
adapted for climbing and holding on. The other half consists, of the
abdomen, together with spinnerets and glands, which secrete the fluid out of
which the web is spun, and this, although it hardens to some extent on
exposure to the air, retains its viscid nature for the purpose of entangling its
prey. The spinnerets are the most interesting feature in the anatomy of the
Epeira (Figs. 410 and 411).
Page 712
Fig. 410.
1. Spinnerets of Spider; 2. Extreme end of one of the upper pair of spinnerets; 3.
End of under pair of spinnerets; 4. Foot of Spider; 5. Side view of eye; 6. The
arrangement of the four pairs of eyes.
Five kinds of spinning glands are found in spiders. The glandulæ
aciniformes are those which consist of a proper tunica and an epithelium;
these exhibit in all parts the same reaction to staining agents. The glandulæ
pyriformes consist of a tunica proper and an epithelium, which in their
lower parts (or those near the efferent ducts) stain more deeply than the
upper. The glandulæ ampullaceæ and glandulæ tubuliformes have similar
coverings, the latter terminating in a large spool. The glandulæ aggregatæ
have a wide and branched lumen, the efferent duct of which is provided
with cells and an accessory piece, which draws out to a tip. All the glands
have secreting portions, which serve as collecting cavities for the spinning
material. The spools are two-jointed basal and one-jointed accessory pieces.
In addition to the five glands enumerated, there are also lobate and
cribelleum glands; these are variously distributed, and exercise different
functions, one set preparing the so-called moist filaments from the moist
droplets, another spins the egg-cocoon, as nearly all spiders envelop their
eggs in a covering of silken threads and store them up in some sheltered
place awaiting the warm weather of spring to hatch them out. The bag that
holds the eggs is not one of the least curious efforts of skill and care. The
1. Spinnerets of Spider; 2. Extreme end of one of the upper pair of spinnerets; 3.
End of under pair of spinnerets; 4. Foot of Spider; 5. Side view of eye; 6. The
arrangement of the four pairs of eyes.
Five kinds of spinning glands are found in spiders. The glandulæ
aciniformes are those which consist of a proper tunica and an epithelium;
these exhibit in all parts the same reaction to staining agents. The glandulæ
pyriformes consist of a tunica proper and an epithelium, which in their
lower parts (or those near the efferent ducts) stain more deeply than the
upper. The glandulæ ampullaceæ and glandulæ tubuliformes have similar
coverings, the latter terminating in a large spool. The glandulæ aggregatæ
have a wide and branched lumen, the efferent duct of which is provided
with cells and an accessory piece, which draws out to a tip. All the glands
have secreting portions, which serve as collecting cavities for the spinning
material. The spools are two-jointed basal and one-jointed accessory pieces.
In addition to the five glands enumerated, there are also lobate and
cribelleum glands; these are variously distributed, and exercise different
functions, one set preparing the so-called moist filaments from the moist
droplets, another spins the egg-cocoon, as nearly all spiders envelop their
eggs in a covering of silken threads and store them up in some sheltered
place awaiting the warm weather of spring to hatch them out. The bag that
holds the eggs is not one of the least curious efforts of skill and care. The
Page 713
mother uses her body as a gauge to measure her work, precisely as a bird
uses her body to gauge the size and form of its nest. The spider first spreads
a thin coating of silk as a foundation, taking care to have this circular by
turning its body round during the process. In the same manner it spins a
raised border round this till it takes the form of a cup; it is at this stage of
the work the female begins to lay her eggs in the cup, and not content to fill
it up to the brim, she also piles up a heap as high as the cup is deep. Here,
then, is a cup full of eggs, the under half covered and protected by the
silken sides of the cup, but the upper still exposed to the air and the cold.
She now sets to work to cover this; the process is similar to the preceding—
that is, she weaves a thick web of silk all round the top, and instead of a
cup-shaped nest, like those of the bird tribe, the whole partakes of the form
of a ball much larger than the body of the spider.
The eight legs and feet of the spider
(one only is represented Fig. 410, No.
4) are curiously constructed. Each
foot, when magnified, is seen to be
armed with strong horny claws, with
serrations on their under-surface. By
this arrangement the spider is enabled
to regulate the issue of its web from
the spinnerets. In addition, a
remarkable comb-like claw is
provided for the purpose of
separating certain threads which enter
into the composition of the delicate
web, so that everything is arranged
and planned in the most geometrical Fig. 411.—Spinnerets of Spider greatly enlarged.
order, while the mouth or jaws with
their two movable poison-fangs convert the Arachnidæ into formidable and
dangerous foes. The maternal industry and instincts of spiders, the
ballooning habits of others, the cave dwellers, with their limited vision,
combined with an increased delicacy of touch and hearing, their disguise of
feigned death when a strong enemy approaches, are all of the most
interesting character.
uses her body to gauge the size and form of its nest. The spider first spreads
a thin coating of silk as a foundation, taking care to have this circular by
turning its body round during the process. In the same manner it spins a
raised border round this till it takes the form of a cup; it is at this stage of
the work the female begins to lay her eggs in the cup, and not content to fill
it up to the brim, she also piles up a heap as high as the cup is deep. Here,
then, is a cup full of eggs, the under half covered and protected by the
silken sides of the cup, but the upper still exposed to the air and the cold.
She now sets to work to cover this; the process is similar to the preceding—
that is, she weaves a thick web of silk all round the top, and instead of a
cup-shaped nest, like those of the bird tribe, the whole partakes of the form
of a ball much larger than the body of the spider.
The eight legs and feet of the spider
(one only is represented Fig. 410, No.
4) are curiously constructed. Each
foot, when magnified, is seen to be
armed with strong horny claws, with
serrations on their under-surface. By
this arrangement the spider is enabled
to regulate the issue of its web from
the spinnerets. In addition, a
remarkable comb-like claw is
provided for the purpose of
separating certain threads which enter
into the composition of the delicate
web, so that everything is arranged
and planned in the most geometrical Fig. 411.—Spinnerets of Spider greatly enlarged.
order, while the mouth or jaws with
their two movable poison-fangs convert the Arachnidæ into formidable and
dangerous foes. The maternal industry and instincts of spiders, the
ballooning habits of others, the cave dwellers, with their limited vision,
combined with an increased delicacy of touch and hearing, their disguise of
feigned death when a strong enemy approaches, are all of the most
interesting character.
Page 714
One of the more remarkable, the Argyroneta aquatica (diving spider),
weaves itself a curious little bell-shaped globule, which it takes with it to
the bottom of the water, whither it retires to devour its prey.
Notwithstanding its aquatic habits, this, like the rest of its species, is fitted
only for aerial respiration; it therefore carries down, entangled amongst the
hairs of its body, a small bubble of air. This contrivance presents us with the
earliest form of diving-bell.
Mites and Ticks constitute a group which for diversity of structure, number
of species and individuals, and minuteness of size, has no equal. The typical
genus of the family—Ixodidæ—being wholly parasitic in their habits, are so
modified in organisation, so marked by degeneration, that some authors
have proposed to remove them into a class by themselves. One leading
character distinguishes the whole: the abdomen rarely presents a trace of
segmentation, but is confluent with the cephalothorax, the fusion between
the two being so complete that, as in the harvest spiders belonging to
Palpatores, the anterior sternal plates of the abdomen are thrust far forward
between the coxæ of the cephalothoracic limbs. As in Arachnidæ, however,
the mouth is adapted for sucking, but the jaws are often partially united, and
form, with a plate termed the epistome and the labium, a beak. The
mandibles are either pincer-like, or simply pointed at the tip, forming
piercing organs; the palpi have their basal segments, or maxillæ, united,
which form a conspicuous plate, or hypostomes, constituting the floor of the
mouth. These organs are often seen to be separated from the rest of the
cephalothorax by a membranous joint, and constitute a kind of head, the
capitulum. In most cases no trace of special respiratory organs can be
found. Another characteristic of value in separating ticks from harvest-
spiders is that in the former the young undergo a metamorphosis in the
course of growth, being hatched as six-footed larvæ, and acquiring later in
life a fourth pair of legs.
The Acariæ include a number of families, all distinguished by the position
of the respiratory stigmata and the form of the mandibles and palpi. In the
velvety mites (Trombidiidæ), the integument is soft and covered with
variously-coloured fine hairs, and the legs are adapted for walking, running
or swimming. The latter live in fresh-water ponds, creeping over the leaves
of aquatic plants. The fresh-water mites (Atax spinipes, Fig. 412) swim
weaves itself a curious little bell-shaped globule, which it takes with it to
the bottom of the water, whither it retires to devour its prey.
Notwithstanding its aquatic habits, this, like the rest of its species, is fitted
only for aerial respiration; it therefore carries down, entangled amongst the
hairs of its body, a small bubble of air. This contrivance presents us with the
earliest form of diving-bell.
Mites and Ticks constitute a group which for diversity of structure, number
of species and individuals, and minuteness of size, has no equal. The typical
genus of the family—Ixodidæ—being wholly parasitic in their habits, are so
modified in organisation, so marked by degeneration, that some authors
have proposed to remove them into a class by themselves. One leading
character distinguishes the whole: the abdomen rarely presents a trace of
segmentation, but is confluent with the cephalothorax, the fusion between
the two being so complete that, as in the harvest spiders belonging to
Palpatores, the anterior sternal plates of the abdomen are thrust far forward
between the coxæ of the cephalothoracic limbs. As in Arachnidæ, however,
the mouth is adapted for sucking, but the jaws are often partially united, and
form, with a plate termed the epistome and the labium, a beak. The
mandibles are either pincer-like, or simply pointed at the tip, forming
piercing organs; the palpi have their basal segments, or maxillæ, united,
which form a conspicuous plate, or hypostomes, constituting the floor of the
mouth. These organs are often seen to be separated from the rest of the
cephalothorax by a membranous joint, and constitute a kind of head, the
capitulum. In most cases no trace of special respiratory organs can be
found. Another characteristic of value in separating ticks from harvest-
spiders is that in the former the young undergo a metamorphosis in the
course of growth, being hatched as six-footed larvæ, and acquiring later in
life a fourth pair of legs.
The Acariæ include a number of families, all distinguished by the position
of the respiratory stigmata and the form of the mandibles and palpi. In the
velvety mites (Trombidiidæ), the integument is soft and covered with
variously-coloured fine hairs, and the legs are adapted for walking, running
or swimming. The latter live in fresh-water ponds, creeping over the leaves
of aquatic plants. The fresh-water mites (Atax spinipes, Fig. 412) swim
Page 715
about freely by means of vigorous
strokes of their legs, which act as
oars. In the adult the body is more or
less spherical, and usually of a bright
red or greenish colour. The males of
one species have a curious blunt tail-
like prolongation from the hinder end
of the abdomen. The eggs are laid in
the spring on the stems of water
Fig. 412. plants, and the six-footed larvæ when
A. Atax spinipes, water mite seen from below; B.
hatched attach themselves to water-
Water Scorpion infested by Atax. bugs (Nepa) or water-beetles
(Dytiscus) by means of a large
sucker developed on the front of the head.
Fig. 413.—Ixodes ricinus or Sheep-tick (under surface). The small circle encloses
one life-size.
strokes of their legs, which act as
oars. In the adult the body is more or
less spherical, and usually of a bright
red or greenish colour. The males of
one species have a curious blunt tail-
like prolongation from the hinder end
of the abdomen. The eggs are laid in
the spring on the stems of water
Fig. 412. plants, and the six-footed larvæ when
A. Atax spinipes, water mite seen from below; B.
hatched attach themselves to water-
Water Scorpion infested by Atax. bugs (Nepa) or water-beetles
(Dytiscus) by means of a large
sucker developed on the front of the head.
Fig. 413.—Ixodes ricinus or Sheep-tick (under surface). The small circle encloses
one life-size.
Page 716
Of all the Acari, the best known and most troublesome are those belonging
to the family Ixodidæ; these infest the whole animal creation. They are
furnished with a long cylindrical beak, armed with recurved hooks, formed
of the two mandibles above and the long slender labium below. They have
no eyes, nor apparently any dermaploptic sense, but there are various
seemingly sensitive setæ distributed over the body and on the appendages.
The whole of the mites will be found suitable objects for the study of
development, as the process is slow and their eggs do not require much
care. The segmentation of the eggs differs; some of the cells are
distinguished by their large nuclei, which stain feebly by carmine. During
the cleavage of the egg no division of the so-called yolk has been observed,
but later on this breaks up into several minute pieces.
The accompanying Fig. 413 shows
the under surface of the body and the
mouth parts of the common English
dog and sheep tick, Ixodes ricinus,
with its six formidable legs. The
upper surface is shown in Fig. 415;
the head (capitulum) and mouth
organs in Fig. 414, c, d, e, f, g,
together with the four segments of
the palpi; h the labial process armed
with hooks forming the lower side of
the beak, and i indicating the tips of
the two mandibles forming the upper
side, and projecting beyond the apex
of the labium. By means of this beak,
which is thrust to its base into the
integument, the tick adheres firmly
to its host, and in detaching them
care must be taken that the head is
not left behind buried in the skin.
This tick is found in all stages of
growth; the females, gorging
Fig 414.—Mouth organs of Sheep-tick. themselves with blood, swell up to
the size of a pea, as seen in Fig. 413,
to the family Ixodidæ; these infest the whole animal creation. They are
furnished with a long cylindrical beak, armed with recurved hooks, formed
of the two mandibles above and the long slender labium below. They have
no eyes, nor apparently any dermaploptic sense, but there are various
seemingly sensitive setæ distributed over the body and on the appendages.
The whole of the mites will be found suitable objects for the study of
development, as the process is slow and their eggs do not require much
care. The segmentation of the eggs differs; some of the cells are
distinguished by their large nuclei, which stain feebly by carmine. During
the cleavage of the egg no division of the so-called yolk has been observed,
but later on this breaks up into several minute pieces.
The accompanying Fig. 413 shows
the under surface of the body and the
mouth parts of the common English
dog and sheep tick, Ixodes ricinus,
with its six formidable legs. The
upper surface is shown in Fig. 415;
the head (capitulum) and mouth
organs in Fig. 414, c, d, e, f, g,
together with the four segments of
the palpi; h the labial process armed
with hooks forming the lower side of
the beak, and i indicating the tips of
the two mandibles forming the upper
side, and projecting beyond the apex
of the labium. By means of this beak,
which is thrust to its base into the
integument, the tick adheres firmly
to its host, and in detaching them
care must be taken that the head is
not left behind buried in the skin.
This tick is found in all stages of
growth; the females, gorging
Fig 414.—Mouth organs of Sheep-tick. themselves with blood, swell up to
the size of a pea, as seen in Fig. 413,
Page 717
c. Capitulum; d, e, f, g. Segments of palpi; h. but the male, formerly regarded as a
Labial process; i. Spiny beak formed of fused
mandibles.—(Warne.) distinct species, is of a much smaller
size. In distribution these pests are
almost cosmopolitan, and in tropical countries they grow to much greater
dimensions, the females sometimes attaining the size of a large gooseberry.
The family of true mites is that of the Sarcoptidæ; these are either free or
parasitic. They have no breathing organs; the palpi are basally fused to the
rostrum, the mandibles are pincer-like, and the tarsi are often furnished at
their tips with a sucker. The most familiar is the cheese mite, Tyroglyphus,
which feeds upon decaying matter.
Fig. 415.
1. Female Sheep-tick; 2. Rat-tick; 3. Head of Cat-flea; 4. Larva of Flea. (The life
size is given in circles.)
Labial process; i. Spiny beak formed of fused
mandibles.—(Warne.) distinct species, is of a much smaller
size. In distribution these pests are
almost cosmopolitan, and in tropical countries they grow to much greater
dimensions, the females sometimes attaining the size of a large gooseberry.
The family of true mites is that of the Sarcoptidæ; these are either free or
parasitic. They have no breathing organs; the palpi are basally fused to the
rostrum, the mandibles are pincer-like, and the tarsi are often furnished at
their tips with a sucker. The most familiar is the cheese mite, Tyroglyphus,
which feeds upon decaying matter.
Fig. 415.
1. Female Sheep-tick; 2. Rat-tick; 3. Head of Cat-flea; 4. Larva of Flea. (The life
size is given in circles.)
Page 718
The well-known cheese mite attains to a size plainly visible to the naked
eye, but when first hatched out from the egg (shown in its several stages of
development in Fig. 417), requires a moderate amount of magnification. Its
growth, however, is rapid and the young begin to feed as soon as they leave
the egg. The body is partially covered over by setæ, or hairs, and the feet
terminate in hooklets, as seen in the full-grown acarus. The mandibles are
cutting, but as a rule they prefer soft and partially-decayed kinds of food. It
also feeds upon damaged flour, sugar, and other domestic articles. The
Dermestes lardarius, one of the minute beetle tribe (Fig. 418), commits
even greater depredations among insect and other collections during the
larval stage of its existence.
Fig. 416.
eye, but when first hatched out from the egg (shown in its several stages of
development in Fig. 417), requires a moderate amount of magnification. Its
growth, however, is rapid and the young begin to feed as soon as they leave
the egg. The body is partially covered over by setæ, or hairs, and the feet
terminate in hooklets, as seen in the full-grown acarus. The mandibles are
cutting, but as a rule they prefer soft and partially-decayed kinds of food. It
also feeds upon damaged flour, sugar, and other domestic articles. The
Dermestes lardarius, one of the minute beetle tribe (Fig. 418), commits
even greater depredations among insect and other collections during the
larval stage of its existence.
Fig. 416.
Page 719
Tyroglyphus. 1. Pediculus vulgaris × 50 diameters; 2. Acarus destructor under
surface; 3. Sarcoptes scabici, Itch-insect, magnified 350 diameters; 4. Demodex
folliculorum from the human skin in various stages of growth, from the egg
upwards, magnified 400 diameters. (The small circles enclose the objects of the
natural size.)
Fig. 417.—The Cheese Mite, Acarus domesticus, seen in its several stages of
development.
Birds suffer much from mites
living parasitically upon them
belonging to Sarcoptidæ; these
likewise infest mankind, and give
rise to a disease known as the
itch (Fig. 416, No. 3). This
malady and the irritation Fig. 418.—Dermestes lardarius: larva, pupa, and
accompanying it are caused by imago. (Natural size.)
the mite excavating tunnels under
the skin. In these the eggs are laid and hatched, and the young then start
burrowing on their own account; their burrows are traced as whitish lines
on the surface of the skin.
Fig. 416, No. 4, Demodex folliculorum, is another remarkable parasite
found beneath the skin; this is usually obtained from a spot where the
surface; 3. Sarcoptes scabici, Itch-insect, magnified 350 diameters; 4. Demodex
folliculorum from the human skin in various stages of growth, from the egg
upwards, magnified 400 diameters. (The small circles enclose the objects of the
natural size.)
Fig. 417.—The Cheese Mite, Acarus domesticus, seen in its several stages of
development.
Birds suffer much from mites
living parasitically upon them
belonging to Sarcoptidæ; these
likewise infest mankind, and give
rise to a disease known as the
itch (Fig. 416, No. 3). This
malady and the irritation Fig. 418.—Dermestes lardarius: larva, pupa, and
accompanying it are caused by imago. (Natural size.)
the mite excavating tunnels under
the skin. In these the eggs are laid and hatched, and the young then start
burrowing on their own account; their burrows are traced as whitish lines
on the surface of the skin.
Fig. 416, No. 4, Demodex folliculorum, is another remarkable parasite
found beneath the skin; this is usually obtained from a spot where the
Page 720
sebaceous follicles or fat glands are abundant, such as the forehead, the side
of the nose, and the angles between the nose and lip. If the part where a
little black spot or a pustule is seen be squeezed rather hard, the oily matter
there accumulated will be forced out in a globular form. This minute mite is
less than one-fiftieth of an inch in length; if it be laid on a glass slide, and a
small quantity of glycerine added to cause the separation of the harder
portions, the parasite in all probability will float out, and, by means of a
fine-pointed pencil or brush, can be transferred to a clean slide and mounted
in Canada balsam. An allied species is found in the skin of dogs suffering
from mange.
Fig. 419.
1. Parasite of Turkey; 2. Acarus of common Fowl, under surface; 3. Parasite of
Pheasant. (The small circles enclose each about life size.)
of the nose, and the angles between the nose and lip. If the part where a
little black spot or a pustule is seen be squeezed rather hard, the oily matter
there accumulated will be forced out in a globular form. This minute mite is
less than one-fiftieth of an inch in length; if it be laid on a glass slide, and a
small quantity of glycerine added to cause the separation of the harder
portions, the parasite in all probability will float out, and, by means of a
fine-pointed pencil or brush, can be transferred to a clean slide and mounted
in Canada balsam. An allied species is found in the skin of dogs suffering
from mange.
Fig. 419.
1. Parasite of Turkey; 2. Acarus of common Fowl, under surface; 3. Parasite of
Pheasant. (The small circles enclose each about life size.)
Page 721
The Stylopidæ are remarkable parasites, living upon the bodies of wasps,
bees, and bugs, and present a type of structure quite distinct from beetles or
the ticks described. The male (Xenos peckii, Fig. 420) is a winged insect
with coarsely faceted eyes, large fan-shaped wings, extremely small
inconspicuous elytra, the two first thoracic rings short, while the metathorax
is elongated and covers the base of the abdomen, and the hind legs are
placed a long way behind the middle pair. The female, on the other hand, is
a grub-like creature, without legs, wings, or eyes; she never leaves the body
of her host, and from her eggs active little larvæ develop and get carried
into the nests of bees and wasps.
Mites are very numerous, differ in
form, and are interesting objects
under the microscope. The body of
the common flea (Fig. 421) is
divided into distinct segments, those
about the thorax being separated.
Although apterous, the flea has the
rudiments of four wings in the form
of horny plates on both sides of the Fig. 420.—Xenos peckii. 1. Male; 2. Female.
thoracic segments. Its mouth consists
of a pair of sword-shaped mandibles, finely serrated; these, with a sharp,
penetrating, needle-like organ, constitute the formidable weapons with
which it pierces through the skin.
The neck is distinctly separated, and the body covered with scales, the
edges of which are beset with short setæ; from the head project a short pair
of antennæ, below which are a proboscis and a lance-shaped cutting
apparatus. On each side of the head a large compound eye is placed; it has
six many-jointed powerful legs, terminating in two-hooked claws; a pair of
long hind legs are kept folded up when the insect is at rest, which, in the act
of jumping, it suddenly straightens out with great muscular force. The
female flea (Fig. 421) lays a great number of eggs, sticking them together
with a glutinous secretion; the flea infesting the dog or cat glues its eggs to
the roots of the hairs. In about four days the eggs are hatched out, and a
small white larva or grub is seen crawling about, and feeding most actively.
Plate VI., No. 141, is a magnified view of one covered with short hairs.
bees, and bugs, and present a type of structure quite distinct from beetles or
the ticks described. The male (Xenos peckii, Fig. 420) is a winged insect
with coarsely faceted eyes, large fan-shaped wings, extremely small
inconspicuous elytra, the two first thoracic rings short, while the metathorax
is elongated and covers the base of the abdomen, and the hind legs are
placed a long way behind the middle pair. The female, on the other hand, is
a grub-like creature, without legs, wings, or eyes; she never leaves the body
of her host, and from her eggs active little larvæ develop and get carried
into the nests of bees and wasps.
Mites are very numerous, differ in
form, and are interesting objects
under the microscope. The body of
the common flea (Fig. 421) is
divided into distinct segments, those
about the thorax being separated.
Although apterous, the flea has the
rudiments of four wings in the form
of horny plates on both sides of the Fig. 420.—Xenos peckii. 1. Male; 2. Female.
thoracic segments. Its mouth consists
of a pair of sword-shaped mandibles, finely serrated; these, with a sharp,
penetrating, needle-like organ, constitute the formidable weapons with
which it pierces through the skin.
The neck is distinctly separated, and the body covered with scales, the
edges of which are beset with short setæ; from the head project a short pair
of antennæ, below which are a proboscis and a lance-shaped cutting
apparatus. On each side of the head a large compound eye is placed; it has
six many-jointed powerful legs, terminating in two-hooked claws; a pair of
long hind legs are kept folded up when the insect is at rest, which, in the act
of jumping, it suddenly straightens out with great muscular force. The
female flea (Fig. 421) lays a great number of eggs, sticking them together
with a glutinous secretion; the flea infesting the dog or cat glues its eggs to
the roots of the hairs. In about four days the eggs are hatched out, and a
small white larva or grub is seen crawling about, and feeding most actively.
Plate VI., No. 141, is a magnified view of one covered with short hairs.
Page 722
After nine or ten days the larva assumes the pupa form; this it retains four
days, and in nine days more it becomes a perfect flea. The head of the flea
found in the cat (Fig. 415, No. 3) somewhat differs in form from that of the
species infesting the human being; its jaws are furnished with more
formidable-looking mandibles, and from between the first and second joints
behind the head short strong spines project.
Fig. 421.
1. Female Flea; 2. Male Flea. (The small circles enclose fleas of about life size.)
days, and in nine days more it becomes a perfect flea. The head of the flea
found in the cat (Fig. 415, No. 3) somewhat differs in form from that of the
species infesting the human being; its jaws are furnished with more
formidable-looking mandibles, and from between the first and second joints
behind the head short strong spines project.
Fig. 421.
1. Female Flea; 2. Male Flea. (The small circles enclose fleas of about life size.)
Page 723
Fig. 422.
1. Parasite of Eagle; 2. Parasite of Vulture; 3. Parasite of Pigeon, Sarcoptes
palumbinus. (The circles enclose each about life size.)
Two small and obscure groups of the mites and ticks have been associated
with the latter, but for no better reason than that their affinities are
unknown. The first of these are the Tardigrada, or bear animalcules, which
comprise microscopical animals living in damp, sandy, and mossy places;
the body is long and oval in shape, and possesses four pairs of bud-like
unjointed appendages, each tipped with claws: the last pair of legs project
from the hinder part of the body. The mouth is much subdued, and only a
trace of jaws is found as a pair of stylets; there appear to be no organs of
respiration or circulation, and, unlike what obtains in all true Arachnida, the
1. Parasite of Eagle; 2. Parasite of Vulture; 3. Parasite of Pigeon, Sarcoptes
palumbinus. (The circles enclose each about life size.)
Two small and obscure groups of the mites and ticks have been associated
with the latter, but for no better reason than that their affinities are
unknown. The first of these are the Tardigrada, or bear animalcules, which
comprise microscopical animals living in damp, sandy, and mossy places;
the body is long and oval in shape, and possesses four pairs of bud-like
unjointed appendages, each tipped with claws: the last pair of legs project
from the hinder part of the body. The mouth is much subdued, and only a
trace of jaws is found as a pair of stylets; there appear to be no organs of
respiration or circulation, and, unlike what obtains in all true Arachnida, the
Page 724
sexes are united in each individual. These curious infusorial creatures have
been found by myself in an infusion of cow manure.
Injurious Insects.—In describing some of the more interesting points in
connection with insect life, I have only quite incidentally referred to the
destructive habits of the larger number of insects and the ravages annually
inflicted, chiefly by the smaller parasitical tribes, upon our cultivated crops
of all kinds.
Here we have a wide field of research open to the microscopist, whose
investigations must be carried out systematically, day by day, and for which
a moderate power will effectually serve his purpose.
There are some ten or twelve species of injurious insects that attack the hop
plant. By way of example, I will select one of the least known among them,
the hop-flea, or beetle (Haltica concinna). This is sufficiently minute to
require the aid of the microscope, and very closely resembles the turnip-flea
proper, H. nemorum. Under the microscope the former will be seen to differ
considerably. Its colour is brassy, whereas the colour of its congener is
dusky or black, and its wing-cases are striped. They both have wonderful
powers of jumping. H. concinna has a curious toothed formation of the
tibia, with a set of spines, while the tibia of the turnip-flea is without any
curve. It presents other points of difference. The hop-flea is, in fact, a
winged beetle, and passes the winter in the perfect state under clods, tufts of
grass, or weeds outside the hop-plantation, and here it lays its eggs. In the
early spring the larvæ are hatched out as a little white maggot, which
immediately makes its way to the hop-plant and burrows into the young
leaves and feeds upon its tissues. Here we have an insect taken at random
from among thousands of others of the most destructive kinds which
annually destroy crops of enormous value to the nation.
been found by myself in an infusion of cow manure.
Injurious Insects.—In describing some of the more interesting points in
connection with insect life, I have only quite incidentally referred to the
destructive habits of the larger number of insects and the ravages annually
inflicted, chiefly by the smaller parasitical tribes, upon our cultivated crops
of all kinds.
Here we have a wide field of research open to the microscopist, whose
investigations must be carried out systematically, day by day, and for which
a moderate power will effectually serve his purpose.
There are some ten or twelve species of injurious insects that attack the hop
plant. By way of example, I will select one of the least known among them,
the hop-flea, or beetle (Haltica concinna). This is sufficiently minute to
require the aid of the microscope, and very closely resembles the turnip-flea
proper, H. nemorum. Under the microscope the former will be seen to differ
considerably. Its colour is brassy, whereas the colour of its congener is
dusky or black, and its wing-cases are striped. They both have wonderful
powers of jumping. H. concinna has a curious toothed formation of the
tibia, with a set of spines, while the tibia of the turnip-flea is without any
curve. It presents other points of difference. The hop-flea is, in fact, a
winged beetle, and passes the winter in the perfect state under clods, tufts of
grass, or weeds outside the hop-plantation, and here it lays its eggs. In the
early spring the larvæ are hatched out as a little white maggot, which
immediately makes its way to the hop-plant and burrows into the young
leaves and feeds upon its tissues. Here we have an insect taken at random
from among thousands of others of the most destructive kinds which
annually destroy crops of enormous value to the nation.
Page 725
Tuffen West, del. Edmund Evans.
Plate VII.
Plate VII.
Page 726
CHAPTER V.
Vertebrata.
The most complicated condition in which matter exists is where, under the
influence of life, it forms bodies with a structure of tubes and cavities in
which fluids are incessantly in motion, and producing continuous changes.
These have been rightly designated “organised bodies,” because of the
various organs they contain. The two principal classes into which organised
bodies have been divided are recognised as vegetable and animal. It was
Bichat who taught that our animal life is double, while our organic life is
single. In organic life, to stop is to die; and the life we have in common with
vegetables never sleeps, and if the circulation of the fluids within the animal
body ceases for a few seconds, it ceases for ever. In the vertebrate body,
however, the combination of organs attains to the highest development, in
striking contrast with that of the class we have previously considered, the
Invertebrata, the animal kingdom being divided into Vertebrates and
Invertebrates.
The Vertebrata are distinguished from all other animals by the circumstance
that a transverse and a vertical section of the body exhibits two cavities
completely separated from one another by a partition. A still more
characteristic feature separates the one from the other; it is the
specialisation of the chief nervous centres, and their peculiar relation to the
other systems of the body.
The dorsal cavity of the body contains the cerebro-spinal nervous system,
the ventral, the alimentary canal, the heart, and usually a double chain of
ganglia; these pass under the name of the sympathetic system. It is very
probable that this sympathetic nervous system represents, wholly or
partially, the principal nervous system of the Annulosa and Mollusca. In any
case, the central parts of the cerebro-spinal nervous system—i.e., the brain
Vertebrata.
The most complicated condition in which matter exists is where, under the
influence of life, it forms bodies with a structure of tubes and cavities in
which fluids are incessantly in motion, and producing continuous changes.
These have been rightly designated “organised bodies,” because of the
various organs they contain. The two principal classes into which organised
bodies have been divided are recognised as vegetable and animal. It was
Bichat who taught that our animal life is double, while our organic life is
single. In organic life, to stop is to die; and the life we have in common with
vegetables never sleeps, and if the circulation of the fluids within the animal
body ceases for a few seconds, it ceases for ever. In the vertebrate body,
however, the combination of organs attains to the highest development, in
striking contrast with that of the class we have previously considered, the
Invertebrata, the animal kingdom being divided into Vertebrates and
Invertebrates.
The Vertebrata are distinguished from all other animals by the circumstance
that a transverse and a vertical section of the body exhibits two cavities
completely separated from one another by a partition. A still more
characteristic feature separates the one from the other; it is the
specialisation of the chief nervous centres, and their peculiar relation to the
other systems of the body.
The dorsal cavity of the body contains the cerebro-spinal nervous system,
the ventral, the alimentary canal, the heart, and usually a double chain of
ganglia; these pass under the name of the sympathetic system. It is very
probable that this sympathetic nervous system represents, wholly or
partially, the principal nervous system of the Annulosa and Mollusca. In any
case, the central parts of the cerebro-spinal nervous system—i.e., the brain
Page 727
and the spinal cord—would appear to be unrepresented among invertebrate
animals. Likewise, in the partition between the cerebro-spinal and visceral
tubes, certain structures which are not represented in Invertebrates are
contained. During the embryonic condition of all Vertebrates, the centre of
the partition is occupied by an elongated cellular cylindrical mass, the
notochord, or chorda dorsalis. This structure persists throughout the life in
some Vertebrata, but in most it is more or less completely replaced by a
jointed, partly fibrous, cartilaginous, and bony vertical column. All
vertebrate animals have a complete vascular system. In the thorax and
abdomen, in place of a single perivisceral cavity, in communication with the
vascular system, and serving as a blood-sinus, there are one or more serous
sacs. These invest the principal viscera, and may or may not communicate
with the exterior, recalling in the latter case the atrial cavities of the
Mollusca. In all Vertebrata, except Amphioxus, there is a single valvular
heart, and all possess a hepatic portal system, the blood of the alimentary
canal never being wholly returned directly to the heart by the ordinary
veins, but being more or less completely collected into a trunk (the portal
vein), which ramifies through and supplies the liver.
With reference to one other point of importance, the development of the ova
of Vertebrates, these have the same primary composition as those of other
animals, consisting of a germinal vesicle containing one or more germinal
nuclei, and included within a vitellus. But as this forms a part of general
anatomy, and as my object is simply the investigation of the fundamental
and microscopical structure of animal organisms, I shall not further pursue
the morphological part of the subject, especially as so many excellent text-
books are within reach of the student who desires to fully acquaint himself
with precise information.
Notwithstanding, then, the apparent diversity in the structure of the
vertebrate and the invertebrate and the various tissues of which animals and
vegetables are constituted, microscopical research has satisfactorily
demonstrated that all textures have their origin in cells; in fact, when the
formative process is complete, the animal cell is seen to consist of the same
parts and almost the same chemical constituents as the typical cell of the
plant—namely, a definite cell-wall enclosing cell contents, of which the
nature may be diverse, but the cell nucleus is precisely the same and is the
animals. Likewise, in the partition between the cerebro-spinal and visceral
tubes, certain structures which are not represented in Invertebrates are
contained. During the embryonic condition of all Vertebrates, the centre of
the partition is occupied by an elongated cellular cylindrical mass, the
notochord, or chorda dorsalis. This structure persists throughout the life in
some Vertebrata, but in most it is more or less completely replaced by a
jointed, partly fibrous, cartilaginous, and bony vertical column. All
vertebrate animals have a complete vascular system. In the thorax and
abdomen, in place of a single perivisceral cavity, in communication with the
vascular system, and serving as a blood-sinus, there are one or more serous
sacs. These invest the principal viscera, and may or may not communicate
with the exterior, recalling in the latter case the atrial cavities of the
Mollusca. In all Vertebrata, except Amphioxus, there is a single valvular
heart, and all possess a hepatic portal system, the blood of the alimentary
canal never being wholly returned directly to the heart by the ordinary
veins, but being more or less completely collected into a trunk (the portal
vein), which ramifies through and supplies the liver.
With reference to one other point of importance, the development of the ova
of Vertebrates, these have the same primary composition as those of other
animals, consisting of a germinal vesicle containing one or more germinal
nuclei, and included within a vitellus. But as this forms a part of general
anatomy, and as my object is simply the investigation of the fundamental
and microscopical structure of animal organisms, I shall not further pursue
the morphological part of the subject, especially as so many excellent text-
books are within reach of the student who desires to fully acquaint himself
with precise information.
Notwithstanding, then, the apparent diversity in the structure of the
vertebrate and the invertebrate and the various tissues of which animals and
vegetables are constituted, microscopical research has satisfactorily
demonstrated that all textures have their origin in cells; in fact, when the
formative process is complete, the animal cell is seen to consist of the same
parts and almost the same chemical constituents as the typical cell of the
plant—namely, a definite cell-wall enclosing cell contents, of which the
nature may be diverse, but the cell nucleus is precisely the same and is the
Page 728
actual seat and origin of all formative activity. The cell and nucleus grow by
assimilation or intersusception, that is, by inflowing of nutrition among all
parts, the new replacing the old, yet maintaining its original structure and
composition. That which was once thought special to animals is now found
to be common to both plants and animals: they are found to be alike
fundamentally in internal structure, and in the discharge of the mysterious
processes of reproduction and of nutrition, although the latter forms a
convenient line of separation. Life in plants goes on indefinitely; cuttings
may be taken without injury to their vigour and duration of life. The same
may be said of some of the lower forms of invertebrate life; for example,
the hydra, the anemone, and some other well-known animals, may be cut
up, divided into several parts, each one of which will form a new animal,
provided a nucleus be included in the section. Nevertheless, the
organisation of the amœba and the hydra is as complete for its purpose as
that of man for his, and the evidence of continuity forbids the drawing of
hard and fast lines, as was formerly done between the two kingdoms, the
animal and vegetable. The amount of similarity or agreement in the
organisation of animals is various. Animals indeed differ from each other in
slight points only, for the discovery of which the microscope must be
brought into requisition. Living matter in its earliest stage and simplest
form appears to the naked eye as a homogeneous structure, but when placed
under the highest powers of the microscope, it is seen not to be so.
But perhaps the most marked feature of the age has been the increasing
attention given to the study of the lower forms of life, using their simpler
structures and more diffuse phenomena to elucidate the more general
properties of living matter. To understand life we must understand
protoplasm. Of this there can be no doubt, as we have seen in a previous
chapter that a whole family, the Monera, consists of this simple living,
microscopic, jelly-like substance, which has not even begun to be
differentiated, as in the amœba, which has as yet no special organs, and
every speck becomes a mouth or a stomach, and which can be turned inside
out and shoot out tongues of jelly to move and feel with. “Reproduction is
the faculty most characteristic of life, and sharply distinguishes the organic
from the inorganic.” It is, then, the corpuscles of protoplasm, called cells
(cellulæ), which have so much interest for the physiologist, and these, like
the cytods, may form independent organisms, which are then termed
assimilation or intersusception, that is, by inflowing of nutrition among all
parts, the new replacing the old, yet maintaining its original structure and
composition. That which was once thought special to animals is now found
to be common to both plants and animals: they are found to be alike
fundamentally in internal structure, and in the discharge of the mysterious
processes of reproduction and of nutrition, although the latter forms a
convenient line of separation. Life in plants goes on indefinitely; cuttings
may be taken without injury to their vigour and duration of life. The same
may be said of some of the lower forms of invertebrate life; for example,
the hydra, the anemone, and some other well-known animals, may be cut
up, divided into several parts, each one of which will form a new animal,
provided a nucleus be included in the section. Nevertheless, the
organisation of the amœba and the hydra is as complete for its purpose as
that of man for his, and the evidence of continuity forbids the drawing of
hard and fast lines, as was formerly done between the two kingdoms, the
animal and vegetable. The amount of similarity or agreement in the
organisation of animals is various. Animals indeed differ from each other in
slight points only, for the discovery of which the microscope must be
brought into requisition. Living matter in its earliest stage and simplest
form appears to the naked eye as a homogeneous structure, but when placed
under the highest powers of the microscope, it is seen not to be so.
But perhaps the most marked feature of the age has been the increasing
attention given to the study of the lower forms of life, using their simpler
structures and more diffuse phenomena to elucidate the more general
properties of living matter. To understand life we must understand
protoplasm. Of this there can be no doubt, as we have seen in a previous
chapter that a whole family, the Monera, consists of this simple living,
microscopic, jelly-like substance, which has not even begun to be
differentiated, as in the amœba, which has as yet no special organs, and
every speck becomes a mouth or a stomach, and which can be turned inside
out and shoot out tongues of jelly to move and feel with. “Reproduction is
the faculty most characteristic of life, and sharply distinguishes the organic
from the inorganic.” It is, then, the corpuscles of protoplasm, called cells
(cellulæ), which have so much interest for the physiologist, and these, like
the cytods, may form independent organisms, which are then termed
Page 729
unicellular. Again, cells form other cells, and a multicellular organism
results, and goes on increasing in geometrical progression. In the Vertebrata
the cell retains its characteristic spheroidal shape, as seen in Fig. 423, and
undergoes division by virtue of its living protoplasmic mass.
results, and goes on increasing in geometrical progression. In the Vertebrata
the cell retains its characteristic spheroidal shape, as seen in Fig. 423, and
undergoes division by virtue of its living protoplasmic mass.
Page 730
Fig. 423.
1. Newly formed cell structure; 2. Division of the nucleus; 3. It changes its
situation in the cell; 4. Subdivides and breaks up; 5. Cell-walls increase in
thickness; 6. Branch out into stellate cells; 7. Two cells coalesce; 8 and 9. Become
multicellular.
Epithelial Cells.—All free surfaces of the human body, both internal and
external, are to a very considerable extent covered by epithelium cells.
These cells are everywhere the same, but with modifications in shape and
arrangement. Epithelial cells are nucleated and always joined by their
surfaces or edges, without, on the external surfaces, the intervention of
connective tissue.
There are four essential varieties:—1. Tesselated; 2. Columnar; 3.
Spheroidal; 4. Ciliated; in all of which the nucleus remains remarkably
uniform in its characters, is either round or oval, and flattened out,
measuring 1⁄6000th to 1⁄4000th of an inch in diameter. They are insoluble in
acetic acid, colourless, or slightly tinted by the structure with which they
are in contact, and usually contain one or more nucleoli with a few minute
irregular granules, as represented in Fig. 424.
The simplest and most commonly distributed variety is the tesselated,
known also as the scaly, squamous, pavement, and flattened epithelium,
always arranged in single layers, lining serous cavities, many parts of the
mucous membrane, and the interior of ducts and blood vessels. Upon the
external surface of the body it occurs in superimposed layers, forming the
1. Newly formed cell structure; 2. Division of the nucleus; 3. It changes its
situation in the cell; 4. Subdivides and breaks up; 5. Cell-walls increase in
thickness; 6. Branch out into stellate cells; 7. Two cells coalesce; 8 and 9. Become
multicellular.
Epithelial Cells.—All free surfaces of the human body, both internal and
external, are to a very considerable extent covered by epithelium cells.
These cells are everywhere the same, but with modifications in shape and
arrangement. Epithelial cells are nucleated and always joined by their
surfaces or edges, without, on the external surfaces, the intervention of
connective tissue.
There are four essential varieties:—1. Tesselated; 2. Columnar; 3.
Spheroidal; 4. Ciliated; in all of which the nucleus remains remarkably
uniform in its characters, is either round or oval, and flattened out,
measuring 1⁄6000th to 1⁄4000th of an inch in diameter. They are insoluble in
acetic acid, colourless, or slightly tinted by the structure with which they
are in contact, and usually contain one or more nucleoli with a few minute
irregular granules, as represented in Fig. 424.
The simplest and most commonly distributed variety is the tesselated,
known also as the scaly, squamous, pavement, and flattened epithelium,
always arranged in single layers, lining serous cavities, many parts of the
mucous membrane, and the interior of ducts and blood vessels. Upon the
external surface of the body it occurs in superimposed layers, forming the
Page 731
“stratified epidermis.” To obtain specimens of lamellar epithelium it is only
necessary to collect a little saliva, or pass a glass slide over the lining
membrane of the cheek, cover it with a thin cover glass, and examine it
with a ¼-inch objective. Pavement epithelium is the elementary structure of
hair, nails, and horn.
PLATE XIX.
ANIMAL TISSUES.
Columnar epithelium exists upon the mucous membrane of the stomach, on
the villi of the intestines, and in the several canals. It occupies either a
vertical or horizontal position, and may be detached in rows, as shown in
Plate XIX., No. 2, a section taken from the intestine of a rabbit. This
variety, when more highly magnified, as in Fig. 424, is seen to consist of
necessary to collect a little saliva, or pass a glass slide over the lining
membrane of the cheek, cover it with a thin cover glass, and examine it
with a ¼-inch objective. Pavement epithelium is the elementary structure of
hair, nails, and horn.
PLATE XIX.
ANIMAL TISSUES.
Columnar epithelium exists upon the mucous membrane of the stomach, on
the villi of the intestines, and in the several canals. It occupies either a
vertical or horizontal position, and may be detached in rows, as shown in
Plate XIX., No. 2, a section taken from the intestine of a rabbit. This
variety, when more highly magnified, as in Fig. 424, is seen to consist of
Page 732
club-shaped nucleated cells, the thicker end being turned towards the
surface. The protoplasm of the cell is granular, and the presence of minute
vacuoles and fatty globules occupy a great part of the space. The nucleus is
now seen to contain a fine network. At times the outer end of the cell is
distended, as in Fig. 3. This form of columnar epithelium (known as the
“goblet” cell) presents a close and remarkable resemblance to the cilio-
flagellate “collared” infusorial monad in its extended “wine-glass” form.
Fig. 424.
No. 1. Pavement epithelium, taken from an internal membrane; 2. Columnar
epithelium, from the intestine of a rabbit, showing central fat globules, and at str a
fine ciliated border; 3. A so-called “goblet”-cell.
Spheroidal epithelium is confined to the closed cavities of the body, and in
the internal structure of the ducts of secreting glands. The cells are, for the
most part, circular, although some are flattened out at the sides in which
they are in contact with each other (Plate XIX., No. 1a). Specimens of this
form may be taken from the internal surface of one of the lower animals
with a scalpel. The collected matter must be placed in a drop of distilled
water and examined with a high power.
Ciliated epithelium is characterised by the presence of those fine hair-like
filaments (cilia) attached to the free surface of the cell. During life, and for
some time after death, the cilia are seen to retain their constant waving
motion. The cilia all move in one direction and rhythmically, thus giving
surface. The protoplasm of the cell is granular, and the presence of minute
vacuoles and fatty globules occupy a great part of the space. The nucleus is
now seen to contain a fine network. At times the outer end of the cell is
distended, as in Fig. 3. This form of columnar epithelium (known as the
“goblet” cell) presents a close and remarkable resemblance to the cilio-
flagellate “collared” infusorial monad in its extended “wine-glass” form.
Fig. 424.
No. 1. Pavement epithelium, taken from an internal membrane; 2. Columnar
epithelium, from the intestine of a rabbit, showing central fat globules, and at str a
fine ciliated border; 3. A so-called “goblet”-cell.
Spheroidal epithelium is confined to the closed cavities of the body, and in
the internal structure of the ducts of secreting glands. The cells are, for the
most part, circular, although some are flattened out at the sides in which
they are in contact with each other (Plate XIX., No. 1a). Specimens of this
form may be taken from the internal surface of one of the lower animals
with a scalpel. The collected matter must be placed in a drop of distilled
water and examined with a high power.
Ciliated epithelium is characterised by the presence of those fine hair-like
filaments (cilia) attached to the free surface of the cell. During life, and for
some time after death, the cilia are seen to retain their constant waving
motion. The cilia all move in one direction and rhythmically, thus giving
Page 733
rise to the appearance of a succession of undulations. Ciliated epithelium is
found lining the mucous membrane of the air passages and nasal ducts, and
wherever it is necessary to urge on a secretion by mechanical means,
ciliated epithelium exists. Specimens for examination are easily obtained
from the oyster, and with care will show the characteristic motion. A portion
of a gill separated from the mollusc will live on for a considerable time if
kept in a little of its natural secretion. The parameciæ, rotifera, and all the
ciliata, are furnished with cilia as a means of locomotion and obtaining
sustenance. By snipping off a small piece from the gills of the mussel,
always accessible to the microscopist, and covering it over with thin glass
to prevent evaporation of the animal juices, its cilia will continue to work
for hours.
Lymph and Blood, Fig. 425 B, a a.—There are other cells in the animal
body which possess a certain amount of resemblance to those confined to
the more superficial structures—i.e., the lymph, chyle, and blood. These
fluids present in one respect a physical uniformity of composition, and a
resemblance in the size of their characteristic corpuscles. Chyle contains
besides the corpuscles of lymph, a quantity of minute granules which
imparts a white colour to the fluid. Intermixed are oil globules, free nuclei,
and sometimes a few red blood discs. Chyle may be had for microscopic
examination by squeezing a little juice from the lymphatic gland of a sheep
just slaughtered.
found lining the mucous membrane of the air passages and nasal ducts, and
wherever it is necessary to urge on a secretion by mechanical means,
ciliated epithelium exists. Specimens for examination are easily obtained
from the oyster, and with care will show the characteristic motion. A portion
of a gill separated from the mollusc will live on for a considerable time if
kept in a little of its natural secretion. The parameciæ, rotifera, and all the
ciliata, are furnished with cilia as a means of locomotion and obtaining
sustenance. By snipping off a small piece from the gills of the mussel,
always accessible to the microscopist, and covering it over with thin glass
to prevent evaporation of the animal juices, its cilia will continue to work
for hours.
Lymph and Blood, Fig. 425 B, a a.—There are other cells in the animal
body which possess a certain amount of resemblance to those confined to
the more superficial structures—i.e., the lymph, chyle, and blood. These
fluids present in one respect a physical uniformity of composition, and a
resemblance in the size of their characteristic corpuscles. Chyle contains
besides the corpuscles of lymph, a quantity of minute granules which
imparts a white colour to the fluid. Intermixed are oil globules, free nuclei,
and sometimes a few red blood discs. Chyle may be had for microscopic
examination by squeezing a little juice from the lymphatic gland of a sheep
just slaughtered.
Page 734
Fig. 425.—Human Blood Corpuscles and Crystals.
A. a a. Red blood corpuscles lying flat on the warm stage; b b. in profile; c c.
arranged in rouleaux; d. crenated; e. rendered spherical by water; I. leucocytes and
white amœboid corpuscles; B. Blood discs of fowl, red and white, others seen in
convexity and with a nucleus. Blood Crystals.—C. Hæmatin from human blood;
D. Hæmatoidin; E. Hæmin; F. Tetrahedral; G. Pentagonal; H. Octahedral crystals
from blood of mouse.
Blood Corpuscles or cells vary considerably in mammals, birds, reptiles,
and fishes. Fig. 102 (page 143) is a microphotograph of a drop of blood
magnified 3,500 times; and Fig. 425, A, shows both red and white discs
drawn to scale, magnified 1,200 diameters. The red corpuscles of human
blood are distinguished by their clearly defined outlines and dark centres.
Each disc is biconcave in form, and hence the whole surface cannot be
focussed at the same time. When the circumference is well illuminated the
centre is dark, but by bringing the objective nearer to the object, the
A. a a. Red blood corpuscles lying flat on the warm stage; b b. in profile; c c.
arranged in rouleaux; d. crenated; e. rendered spherical by water; I. leucocytes and
white amœboid corpuscles; B. Blood discs of fowl, red and white, others seen in
convexity and with a nucleus. Blood Crystals.—C. Hæmatin from human blood;
D. Hæmatoidin; E. Hæmin; F. Tetrahedral; G. Pentagonal; H. Octahedral crystals
from blood of mouse.
Blood Corpuscles or cells vary considerably in mammals, birds, reptiles,
and fishes. Fig. 102 (page 143) is a microphotograph of a drop of blood
magnified 3,500 times; and Fig. 425, A, shows both red and white discs
drawn to scale, magnified 1,200 diameters. The red corpuscles of human
blood are distinguished by their clearly defined outlines and dark centres.
Each disc is biconcave in form, and hence the whole surface cannot be
focussed at the same time. When the circumference is well illuminated the
centre is dark, but by bringing the objective nearer to the object, the
Page 735
concavity of the disc is brought into focus. It generally happens that blood
corpuscles, on being first drawn, run together, and present the appearance of
rolls of coins; or they may be scattered about over the field. There is a
considerable difference in the form of the discs; they are circular in all
mammals, except the camel, dromedary, and llama, these being oval. In
profile blood corpuscles are biconcave, their investing membrane is
homogeneous and elastic, and will readily move along the smallest capillary
vessels. There is no trace of a nucleus in the blood-discs of the adult
Mammalia, while in size they bear no proportion to the bulk of the animal
in whose blood-vessels they circulate. The corpuscles of Mammalia in
general are like those of man in form and size, being either a little larger or
smaller. The most marked exception is the blood of the musk-deer, in which
the corpuscles are of extreme smallness, about the 1⁄12000th of an inch in
diameter. In the elephant they are large, about 1⁄2700th of an inch in diameter.
The goat, among common animals, has very small corpuscles, but they are,
withal, twice as large as those of the musk-deer. In the Menobranchus
lateralis they are of a much larger size than in any animal, being the 1⁄350th
of an inch; in the proteus, the 1⁄400th of an inch in the longest diameter; in the
salamander, or water-newt, 1⁄600th; in the frog, 1⁄900th; lizards, 1⁄1400th; in birds,
1⁄1700th; and in man, 1⁄3200th of an inch. Of fishes, the cartilaginous have the
largest corpuscles; in gold-fish, they are about the 1⁄1700th of an inch in their
longest diameter.
The large size of the blood discs in reptiles, especially in the Batrachia, has
been of great service to physiologists by enabling them to ascertain many
particulars regarding structure which could not have been otherwise
determined with certainty. The value of the spectroscope in the chemical
examination of the blood has been already referred to. See page 252.
White corpuscles or leucocytes (Fig. 425, I) differ materially from the red.
They are large, spheroidal, finely granular masses of about 1⁄2800th of an inch
in diameter. In a cubic millimètre of human blood there are about 10,000
white corpuscles. They have a lower specific gravity than the red, have no
cell-wall, and their substance mainly consists of protoplasm. The internal
granular appearance is now believed to be due to a fine intercellular
network having small dots at the intersections of the web. In the meshes of
the net a hyaline substance is interspersed. They possess one or more
corpuscles, on being first drawn, run together, and present the appearance of
rolls of coins; or they may be scattered about over the field. There is a
considerable difference in the form of the discs; they are circular in all
mammals, except the camel, dromedary, and llama, these being oval. In
profile blood corpuscles are biconcave, their investing membrane is
homogeneous and elastic, and will readily move along the smallest capillary
vessels. There is no trace of a nucleus in the blood-discs of the adult
Mammalia, while in size they bear no proportion to the bulk of the animal
in whose blood-vessels they circulate. The corpuscles of Mammalia in
general are like those of man in form and size, being either a little larger or
smaller. The most marked exception is the blood of the musk-deer, in which
the corpuscles are of extreme smallness, about the 1⁄12000th of an inch in
diameter. In the elephant they are large, about 1⁄2700th of an inch in diameter.
The goat, among common animals, has very small corpuscles, but they are,
withal, twice as large as those of the musk-deer. In the Menobranchus
lateralis they are of a much larger size than in any animal, being the 1⁄350th
of an inch; in the proteus, the 1⁄400th of an inch in the longest diameter; in the
salamander, or water-newt, 1⁄600th; in the frog, 1⁄900th; lizards, 1⁄1400th; in birds,
1⁄1700th; and in man, 1⁄3200th of an inch. Of fishes, the cartilaginous have the
largest corpuscles; in gold-fish, they are about the 1⁄1700th of an inch in their
longest diameter.
The large size of the blood discs in reptiles, especially in the Batrachia, has
been of great service to physiologists by enabling them to ascertain many
particulars regarding structure which could not have been otherwise
determined with certainty. The value of the spectroscope in the chemical
examination of the blood has been already referred to. See page 252.
White corpuscles or leucocytes (Fig. 425, I) differ materially from the red.
They are large, spheroidal, finely granular masses of about 1⁄2800th of an inch
in diameter. In a cubic millimètre of human blood there are about 10,000
white corpuscles. They have a lower specific gravity than the red, have no
cell-wall, and their substance mainly consists of protoplasm. The internal
granular appearance is now believed to be due to a fine intercellular
network having small dots at the intersections of the web. In the meshes of
the net a hyaline substance is interspersed. They possess one or more
Page 736
nuclei; these are seen on the application of a few drops of acetic acid. When
examined in a perfectly fresh state, especially if the glass slide be placed on
the warm stage of the microscope, they exhibit a spontaneous change of
shape, amœba-like, such movements being accordingly termed amœboid.
The movements referred to consist in the protrusion of processes of
protoplasm which are retracted and other processes protruded as
represented (Fig. 425, I). Both in human blood and in newts there are
colourless corpuscles which contain coarser granules than others; these are
called granular corpuscles. Some are shown near the amœboid bodies. The
white corpuscles are readily found in various tissues of the body, as in the
lymphatic glands. In inflammatory diseases these leucocytes pass through
the walls of the capillaries into the tissues, and form morbid products, pus-
cells.
Sections of blood discs are made by dipping a fine needle in a drop of blood
as it exudes from a prick of the finger and drawing thin lines across the
glass slip, allowing time to dry, and then cutting the lines across in all
directions with a razor. The loosened portions should be removed with a
camel’s-hair brush.
In birds, the blood discs are oval in shape and possess a nucleus, shown in
Fig. 425 B, in the blood of the fowl; this is rendered more apparent on
adding a drop of acetic acid. The blood of fishes is also oval and nucleated,
rather more pointed than that of birds. In reptiles generally the red blood
discs are large, oval, nucleated bodies, the white corpuscles still preserving
their invariable circular form and granular appearance. In the salamander
and proteus the discs attain to their greatest size. In the former they measure
1⁄700th of an inch, and in the latter 1⁄400th.
Blood Crystals.—In addition to the elements described, the blood contains
various crystalline forms, represented in Fig. 425, C to H. In connection
with the micro-spectroscope (p. 253), the spectra of certain blood crystals
are given; although varying in different animals, sufficient uniformity
prevails as to render them characteristic. The crystals are formed when a
little blood is mixed with water on the slide, allowing a short time for
crystallisation. Near the edge of the cover-glass, where crystals begin to
form, they are more distinct, but a high power is required for their
examined in a perfectly fresh state, especially if the glass slide be placed on
the warm stage of the microscope, they exhibit a spontaneous change of
shape, amœba-like, such movements being accordingly termed amœboid.
The movements referred to consist in the protrusion of processes of
protoplasm which are retracted and other processes protruded as
represented (Fig. 425, I). Both in human blood and in newts there are
colourless corpuscles which contain coarser granules than others; these are
called granular corpuscles. Some are shown near the amœboid bodies. The
white corpuscles are readily found in various tissues of the body, as in the
lymphatic glands. In inflammatory diseases these leucocytes pass through
the walls of the capillaries into the tissues, and form morbid products, pus-
cells.
Sections of blood discs are made by dipping a fine needle in a drop of blood
as it exudes from a prick of the finger and drawing thin lines across the
glass slip, allowing time to dry, and then cutting the lines across in all
directions with a razor. The loosened portions should be removed with a
camel’s-hair brush.
In birds, the blood discs are oval in shape and possess a nucleus, shown in
Fig. 425 B, in the blood of the fowl; this is rendered more apparent on
adding a drop of acetic acid. The blood of fishes is also oval and nucleated,
rather more pointed than that of birds. In reptiles generally the red blood
discs are large, oval, nucleated bodies, the white corpuscles still preserving
their invariable circular form and granular appearance. In the salamander
and proteus the discs attain to their greatest size. In the former they measure
1⁄700th of an inch, and in the latter 1⁄400th.
Blood Crystals.—In addition to the elements described, the blood contains
various crystalline forms, represented in Fig. 425, C to H. In connection
with the micro-spectroscope (p. 253), the spectra of certain blood crystals
are given; although varying in different animals, sufficient uniformity
prevails as to render them characteristic. The crystals are formed when a
little blood is mixed with water on the slide, allowing a short time for
crystallisation. Near the edge of the cover-glass, where crystals begin to
form, they are more distinct, but a high power is required for their
Page 737
examination. In human blood the crystals are prismatic; in that of the
guinea-pig, tetrahedral; in the blood of the mouse, octahedral. Other forms
may be obtained by the aid of chemical reagents.
In human blood there are at least three distinct forms of crystals: Hæmatin
is formed in normal blood, is made visible on the addition of a little water
to blood, or by agitation with ether, so as to dissolve the cell-wall of the
blood corpuscles, and allow the contents to escape. A drop of blood will
furnish crystals large enough to be seen with a moderate power.
Hæmatoidin crystals are abnormal products, found in connection with
certain diseased conditions. These crystals are seen as represented at D.
Hæmin crystals must be regarded as artificial chemical products, the result
of treating blood with glacial acetic acid; the acicular crystals at E, reddish-
brown in colour, are artificially produced.
Fig. 426.
1. White fibrous or non-elastic tissue; 2. Yellow fibrous elastic tissue.
Basement Membrane—Connective Tissue System.—Connective or areolar
tissue is present almost throughout the whole of the human body, and serves
to connect the various organs with one another, as well as to bind together
the several parts. The muscles are surrounded by a connective tissue sheath;
guinea-pig, tetrahedral; in the blood of the mouse, octahedral. Other forms
may be obtained by the aid of chemical reagents.
In human blood there are at least three distinct forms of crystals: Hæmatin
is formed in normal blood, is made visible on the addition of a little water
to blood, or by agitation with ether, so as to dissolve the cell-wall of the
blood corpuscles, and allow the contents to escape. A drop of blood will
furnish crystals large enough to be seen with a moderate power.
Hæmatoidin crystals are abnormal products, found in connection with
certain diseased conditions. These crystals are seen as represented at D.
Hæmin crystals must be regarded as artificial chemical products, the result
of treating blood with glacial acetic acid; the acicular crystals at E, reddish-
brown in colour, are artificially produced.
Fig. 426.
1. White fibrous or non-elastic tissue; 2. Yellow fibrous elastic tissue.
Basement Membrane—Connective Tissue System.—Connective or areolar
tissue is present almost throughout the whole of the human body, and serves
to connect the various organs with one another, as well as to bind together
the several parts. The muscles are surrounded by a connective tissue sheath;
Page 738
this penetrates into their substance, and binds together fasciculi and fibres.
The same tissue is present in the skin and the mucous membranes; it also
forms a sheath for the arteries, veins, and nerves. It is plentifully supplied
by blood-vessels, and nerves pass through its substance. Microscopically,
four different elements can be clearly made out:—1. Connective tissue cells
or corpuscles; 2. White fibrous tissue; 3. Yellow fibrous tissue; 4. Ground
substance.
On examining the connective tissue cells of young animals, various cells
will be seen with fine granular contents, together with nuclei, lying in
spaces in the ground substance, some branched, others flattened or rounded.
Even tissues supposed to be homogeneous in structure, are on staining seen
to have connective tissue cells, such as those represented in a section of the
cornea of the eye (see p. 31). In this case the connective tissue cells are
termed corneal corpuscles; the branched cells, it will be noticed, are united
by branches.
The cells in the fibrous tissue of tendons are square or oblong, and form
continuous rows. White fibrous tissue is distributed throughout the animal
body, but in a variety of forms; it is found in the skin and other membranes,
and in all parts where strength and flexibility are necessary. The structure of
white and yellow fibrous tissues is shown in Figs. 426 and 427.
Fig. 427.
The same tissue is present in the skin and the mucous membranes; it also
forms a sheath for the arteries, veins, and nerves. It is plentifully supplied
by blood-vessels, and nerves pass through its substance. Microscopically,
four different elements can be clearly made out:—1. Connective tissue cells
or corpuscles; 2. White fibrous tissue; 3. Yellow fibrous tissue; 4. Ground
substance.
On examining the connective tissue cells of young animals, various cells
will be seen with fine granular contents, together with nuclei, lying in
spaces in the ground substance, some branched, others flattened or rounded.
Even tissues supposed to be homogeneous in structure, are on staining seen
to have connective tissue cells, such as those represented in a section of the
cornea of the eye (see p. 31). In this case the connective tissue cells are
termed corneal corpuscles; the branched cells, it will be noticed, are united
by branches.
The cells in the fibrous tissue of tendons are square or oblong, and form
continuous rows. White fibrous tissue is distributed throughout the animal
body, but in a variety of forms; it is found in the skin and other membranes,
and in all parts where strength and flexibility are necessary. The structure of
white and yellow fibrous tissues is shown in Figs. 426 and 427.
Fig. 427.
Page 739
1. White fibrous tissue lining the interior of the egg shell, with the calcium
carbonate removed by immersion in hydrochloric acid; 2. White fibrous tissue,
from the sclerotic coat of the eye.
White fibrous tissue presents silver-lustre bundles, running for the most part
in parallel directions through and over the muscles and tendons. For
examination under the microscope, obtain a fragment of fresh meat cut in
the longitudinal direction; place it in water, and tease it out with needles as
directed in a former chapter. The smallest fragment will suffice for
examination under a quarter or one-sixth inch objective. These filaments are
exceedingly minute, measuring 1⁄3000th to 1⁄2500th of an inch in diameter, and
do not interlace through the bundles, although they intersect each other
occasionally. Transverse sections may be made by drying a piece of tendon
until it becomes sufficiently firm to cut with a razor or microtome, and
mounted as a permanent specimen. From the cut ends of the fibres small
dark points will be seen, especially in the denser structure of the tendons;
these are termed “connective tissue corpuscles.”
Yellow elastic fibrous tissue is remarkable in contradistinction to the white
for its elasticity and capability of extension. It is found on the coats of
blood-vessels, between the vertebral arches, and in quadrupeds it forms a
strong elastic band, extending from the occiput, throughout the spines of the
vertebra, and enabling the animal to support the head in the pendent
position, without muscular exertion. These fibres can only be separated
from each other with difficulty, and their elasticity is shown by a tendency
to curl up. These yellow fibres are somewhat coarser than the white, and
they remain unaffected by acetic acid of the ordinary strength. Elastic tissue
is a constituent of the skin, mucous, and serous membranes, and of the
areolar or cellular tissue.
In order to microscopically examine this structure, take a small portion of
the strong ligament of the neck of the ox, place it as before in water, and
tease it out with needles; place a fragment on a glass slip, cover with a thin
cover-glass, and submit it to a high magnifying power. Transverse sections
made as directed in the case of white tissue will be seen to be hexagonal in
form.
carbonate removed by immersion in hydrochloric acid; 2. White fibrous tissue,
from the sclerotic coat of the eye.
White fibrous tissue presents silver-lustre bundles, running for the most part
in parallel directions through and over the muscles and tendons. For
examination under the microscope, obtain a fragment of fresh meat cut in
the longitudinal direction; place it in water, and tease it out with needles as
directed in a former chapter. The smallest fragment will suffice for
examination under a quarter or one-sixth inch objective. These filaments are
exceedingly minute, measuring 1⁄3000th to 1⁄2500th of an inch in diameter, and
do not interlace through the bundles, although they intersect each other
occasionally. Transverse sections may be made by drying a piece of tendon
until it becomes sufficiently firm to cut with a razor or microtome, and
mounted as a permanent specimen. From the cut ends of the fibres small
dark points will be seen, especially in the denser structure of the tendons;
these are termed “connective tissue corpuscles.”
Yellow elastic fibrous tissue is remarkable in contradistinction to the white
for its elasticity and capability of extension. It is found on the coats of
blood-vessels, between the vertebral arches, and in quadrupeds it forms a
strong elastic band, extending from the occiput, throughout the spines of the
vertebra, and enabling the animal to support the head in the pendent
position, without muscular exertion. These fibres can only be separated
from each other with difficulty, and their elasticity is shown by a tendency
to curl up. These yellow fibres are somewhat coarser than the white, and
they remain unaffected by acetic acid of the ordinary strength. Elastic tissue
is a constituent of the skin, mucous, and serous membranes, and of the
areolar or cellular tissue.
In order to microscopically examine this structure, take a small portion of
the strong ligament of the neck of the ox, place it as before in water, and
tease it out with needles; place a fragment on a glass slip, cover with a thin
cover-glass, and submit it to a high magnifying power. Transverse sections
made as directed in the case of white tissue will be seen to be hexagonal in
form.
Page 740
Adipose Tissue.—Fat is found in many situations in the animal body, and on
examination is seen to consist entirely of vesicles, distributed through a
delicate membrane of connective tissue, shown in Plate XIX., Nos. 4 and 5.
On pressure, the circular or oval form of the cells becomes polyhedral;
occasionally the fatty acids in the interior of the vesicles crystallise, and
give rise to a star-like appearance. For the examination of adipose tissue,
take a portion of the mesentery of any small animal—a mouse, or rat.
Retiform Tissue.—Adenoid, or retiform tissue, consists of a delicate
network of connective tissue corpuscles, joining their branches together.
This forms the stroma or framework of lymphoid tissue. It is found in
connection with all the lymphatic glands, spleen, &c. Plate XIX., No. 3, a b,
shows small sections of a lymphatic, together with capillary vessels.
Muscular Fibre.—There are two varieties of muscular fibre in the body—
i.e., striated, and non-striated. The striated is formed in muscles attached to
bony structures, as those of the arm and leg, and in some of the soft
structures, as the tongue, palate, œsophagus, in short, all muscles under the
control of the will. Striped muscle is of a dull red colour and marked with
peculiar longitudinal furrows on its surface. Voluntary muscle consists of:—
1, a connective tissue sheath; 2, fasciculi; 3, fibres and sarcolemma; 4,
discs, fibrilla and sarcous elements. These are shown in connection with
other tissues in Plate XIX., Nos. 11 and 12, and also in Fig. 428 (1, 2, 3).
Fig. 428.
1. Muscular fibre broken across, the fragments connected by the connective tissue
membrane × 100; 2. Fibre broken up into irregular distinct bands: a few blood
examination is seen to consist entirely of vesicles, distributed through a
delicate membrane of connective tissue, shown in Plate XIX., Nos. 4 and 5.
On pressure, the circular or oval form of the cells becomes polyhedral;
occasionally the fatty acids in the interior of the vesicles crystallise, and
give rise to a star-like appearance. For the examination of adipose tissue,
take a portion of the mesentery of any small animal—a mouse, or rat.
Retiform Tissue.—Adenoid, or retiform tissue, consists of a delicate
network of connective tissue corpuscles, joining their branches together.
This forms the stroma or framework of lymphoid tissue. It is found in
connection with all the lymphatic glands, spleen, &c. Plate XIX., No. 3, a b,
shows small sections of a lymphatic, together with capillary vessels.
Muscular Fibre.—There are two varieties of muscular fibre in the body—
i.e., striated, and non-striated. The striated is formed in muscles attached to
bony structures, as those of the arm and leg, and in some of the soft
structures, as the tongue, palate, œsophagus, in short, all muscles under the
control of the will. Striped muscle is of a dull red colour and marked with
peculiar longitudinal furrows on its surface. Voluntary muscle consists of:—
1, a connective tissue sheath; 2, fasciculi; 3, fibres and sarcolemma; 4,
discs, fibrilla and sarcous elements. These are shown in connection with
other tissues in Plate XIX., Nos. 11 and 12, and also in Fig. 428 (1, 2, 3).
Fig. 428.
1. Muscular fibre broken across, the fragments connected by the connective tissue
membrane × 100; 2. Fibre broken up into irregular distinct bands: a few blood
Page 741
corpuscles distributed about × 200; 3. A fasciculus of muscular fibre from leg of
pig × 600.
In Plate XIX., Fig. 11, the muscular fibre taken from the tongue of a lamb
shows the continuity of the upper portion with the connective tissue
membrane. In Fig. 12, a branching-out bundle of muscular fibre, taken from
the upper lip of the rat, is seen to end in stellate connective cells. The
delicate homogeneous sheath that binds the fibres together is termed
sarcolemma. This is readily seen in prepared muscle of the frog and water-
beetle, less plainly in man. Each muscle is provided with a sheath of
connective tissue; this surrounds it, binds the fasciculi together, and
supports the blood-vessels; it is called the perimysium, and sends fine
prolongations in between the fibres, termed endomysium. The intervals seen
on high amplification between the dark striæ are called Kruse’s membrane.
On breaking up the striated structure it is resolvable into fibrillæ and
furthermore into discs.
Fig. 429.
1. Vertical section of epidermis; 2. Pigment cells from a lower layer of cutis.
Among mammalia the pig furnishes the best examples of muscle fibrillæ;
among insects the water-beetle and the thorax of the housefly. A power of
600 or 800 diameters is required to separate the fibrillæ. Blood-vessels are
well supplied with striated muscle, but none of their minuter branches
pig × 600.
In Plate XIX., Fig. 11, the muscular fibre taken from the tongue of a lamb
shows the continuity of the upper portion with the connective tissue
membrane. In Fig. 12, a branching-out bundle of muscular fibre, taken from
the upper lip of the rat, is seen to end in stellate connective cells. The
delicate homogeneous sheath that binds the fibres together is termed
sarcolemma. This is readily seen in prepared muscle of the frog and water-
beetle, less plainly in man. Each muscle is provided with a sheath of
connective tissue; this surrounds it, binds the fasciculi together, and
supports the blood-vessels; it is called the perimysium, and sends fine
prolongations in between the fibres, termed endomysium. The intervals seen
on high amplification between the dark striæ are called Kruse’s membrane.
On breaking up the striated structure it is resolvable into fibrillæ and
furthermore into discs.
Fig. 429.
1. Vertical section of epidermis; 2. Pigment cells from a lower layer of cutis.
Among mammalia the pig furnishes the best examples of muscle fibrillæ;
among insects the water-beetle and the thorax of the housefly. A power of
600 or 800 diameters is required to separate the fibrillæ. Blood-vessels are
well supplied with striated muscle, but none of their minuter branches
Page 742
penetrate the sarcolemma. The involuntary or non-striated variety of
muscular fibre exists in all parts of the body where movements occur
independently of the will, also in the ciliary muscle and the iris of the eye,
as well as in the middle coats of the arteries. Non-striated fibres are pale in
colour, prismatic in shape, and easily flattened by pressure. In size, they
vary from 1⁄7000th to 1⁄3500th of an inch in diameter, and are marked at short
intervals by oblong corpuscles.
The Integument or Skin consists of epidermis or cuticle, dermis, corium or
cutis vera, sweat-glands, nails, hairs, sebaceous glands, and numerous
nerves and vessels. The epidermis forms a protective covering over the
whole surface of the body, and is moulded on to the surface of the corium
beneath, covering the ridges, depressions and papillæ. It is made up of three
principal layers: the horny layer or stratium corneum, the most superficial,
this consists of layers of flattened cells, which are without a nucleus; the
stratum lucidum, composed of layers of nucleated cells, more or less
indistinct in section; the rete mucosum or malpighian layer; is composed in
its upper part of layers of “prickle cells” and its inferior of a single stratum
of columnar cells. Pigment is principally found in the lowest layer, Fig. 429.
The gradations of colour in the skin are due to the granular contents of the
pigment cells. This is seen on steeping sections cut from the skin of a negro
in chlorine; the colour is discharged. In Plate XIX., No. 13, the pigment
cells of the choroid coat of eye are shown. Here the pigment is darker in
colour, and its function is the absorption of light and the prevention of
disturbing effects occasioned by circles of dispersion.
muscular fibre exists in all parts of the body where movements occur
independently of the will, also in the ciliary muscle and the iris of the eye,
as well as in the middle coats of the arteries. Non-striated fibres are pale in
colour, prismatic in shape, and easily flattened by pressure. In size, they
vary from 1⁄7000th to 1⁄3500th of an inch in diameter, and are marked at short
intervals by oblong corpuscles.
The Integument or Skin consists of epidermis or cuticle, dermis, corium or
cutis vera, sweat-glands, nails, hairs, sebaceous glands, and numerous
nerves and vessels. The epidermis forms a protective covering over the
whole surface of the body, and is moulded on to the surface of the corium
beneath, covering the ridges, depressions and papillæ. It is made up of three
principal layers: the horny layer or stratium corneum, the most superficial,
this consists of layers of flattened cells, which are without a nucleus; the
stratum lucidum, composed of layers of nucleated cells, more or less
indistinct in section; the rete mucosum or malpighian layer; is composed in
its upper part of layers of “prickle cells” and its inferior of a single stratum
of columnar cells. Pigment is principally found in the lowest layer, Fig. 429.
The gradations of colour in the skin are due to the granular contents of the
pigment cells. This is seen on steeping sections cut from the skin of a negro
in chlorine; the colour is discharged. In Plate XIX., No. 13, the pigment
cells of the choroid coat of eye are shown. Here the pigment is darker in
colour, and its function is the absorption of light and the prevention of
disturbing effects occasioned by circles of dispersion.
Page 743
Fig. 430.—Vertical section of skin and subcutaneous tissues, showing the sweat-
glands and fat-globules, ducts passing upwards to the epidermis or external cuticle.
Magnified 250 diameters.
The Dermis, or true skin, consists of an interlacing network of connective
tissue, yellow elastic tissue corpuscles, vessels, and nerves. There are also
small muscular fibres in connection with the hair follicles, and beneath the
subcutaneous tissues contain an abundant supply of fat adipose tissue.
Numerous ridges are seen on the surface, especially on the palm of the hand
and sole of the foot, caused by rows of little elevations of the cutis vera,
termed papillæ. These are more or less conical, and contain a capillary loop,
nerve, and touch corpuscle, which serve to increase the sensitiveness of the
part, lodging a touch corpuscle in a favourable position for receiving
sensations of touch, Fig. 430.
Sweat glands are situated in the subcutaneous tissue, and consist of fine
tubes, which form the duct (seen in the section, Fig. 430); these are
continuous with a blind extremity, coiled up into a ball one-sixtieth of an
inch in diameter, and surrounded by a plexus of capillaries to form the
glands and fat-globules, ducts passing upwards to the epidermis or external cuticle.
Magnified 250 diameters.
The Dermis, or true skin, consists of an interlacing network of connective
tissue, yellow elastic tissue corpuscles, vessels, and nerves. There are also
small muscular fibres in connection with the hair follicles, and beneath the
subcutaneous tissues contain an abundant supply of fat adipose tissue.
Numerous ridges are seen on the surface, especially on the palm of the hand
and sole of the foot, caused by rows of little elevations of the cutis vera,
termed papillæ. These are more or less conical, and contain a capillary loop,
nerve, and touch corpuscle, which serve to increase the sensitiveness of the
part, lodging a touch corpuscle in a favourable position for receiving
sensations of touch, Fig. 430.
Sweat glands are situated in the subcutaneous tissue, and consist of fine
tubes, which form the duct (seen in the section, Fig. 430); these are
continuous with a blind extremity, coiled up into a ball one-sixtieth of an
inch in diameter, and surrounded by a plexus of capillaries to form the
Page 744
gland (Fig. 431, No. 2). Between the layer of columnar cells and the
limiting membrane is a layer of non-striated muscle, and beneath the rite
mucosum there are several layers of polyhedral cells, and an external and
internal limiting membrane; the epithelium of the duct is at its mouth
continuous with the epithelium of the epidermis.
Fig. 431.
1. Blood vessels of papillæ supplied to cutis; 2. Perpendicular section through the
scalp, with two hair-sacs; a. epidermis; b. cutis; c. muscles of the hair follicles.
Nails consist of a root and body, the lunular of which is the whitish portion
of the body near the root, where the skin beneath is less vascular than any
other portion of the finger. The nail closely resembles the epidermis, and
consists of hard and thin layers of cells on the surface, and round, moist
cells beneath. Posteriorly the nail fits into a groove which lodges its root.
The part to which the nail is attached is known as the nail-bed. The
stratified appearance produced by the coalescence of the cells, and their
lying over each other, is shown in Plate VII., No. 149, the toe of the mouse;
while the special arrangement of tissue is better seen under polarised light
(Plate VIII., No. 174).
Hairs consist of a shaft and root. The shaft is cylindrical, and covered with
a layer of imbricated scales, arranged with their edges upwards. The
substance of the hair consists of fibres, or elongated fusiform cells, in which
nuclei are seen. There are present in some hairs (Fig. 432) small air spaces
or lacunæ. In the coarser hair of the body there is a pith (medulla), occupied
by small angular cells and fat granules.
limiting membrane is a layer of non-striated muscle, and beneath the rite
mucosum there are several layers of polyhedral cells, and an external and
internal limiting membrane; the epithelium of the duct is at its mouth
continuous with the epithelium of the epidermis.
Fig. 431.
1. Blood vessels of papillæ supplied to cutis; 2. Perpendicular section through the
scalp, with two hair-sacs; a. epidermis; b. cutis; c. muscles of the hair follicles.
Nails consist of a root and body, the lunular of which is the whitish portion
of the body near the root, where the skin beneath is less vascular than any
other portion of the finger. The nail closely resembles the epidermis, and
consists of hard and thin layers of cells on the surface, and round, moist
cells beneath. Posteriorly the nail fits into a groove which lodges its root.
The part to which the nail is attached is known as the nail-bed. The
stratified appearance produced by the coalescence of the cells, and their
lying over each other, is shown in Plate VII., No. 149, the toe of the mouse;
while the special arrangement of tissue is better seen under polarised light
(Plate VIII., No. 174).
Hairs consist of a shaft and root. The shaft is cylindrical, and covered with
a layer of imbricated scales, arranged with their edges upwards. The
substance of the hair consists of fibres, or elongated fusiform cells, in which
nuclei are seen. There are present in some hairs (Fig. 432) small air spaces
or lacunæ. In the coarser hair of the body there is a pith (medulla), occupied
by small angular cells and fat granules.
Page 745
Fig. 432.
1. Single Hair-root and Shaft; 2. Vertical section, showing fibrous character of the
hair together with colouring matter, external edges serrated; 3. Transverse section
of human hair, medullary substance, and central pith.
The root of the hair is seen to dilate that it may fit more firmly into the skin
hair-follicle. The latter consists of two coats, an outer and an inner,
continuous with the epidermis, and this is called the root sheath. The outer
portion consists of three layers, formed of connective tissue, blood-vessels,
and nerves. The inner, or epidermic, coat comes away when the hair is
pulled out, and hence is called the root sheath. This again is made up of two
layers, the outer of which corresponds with the horny layer, and is
composed of flattened cells. The bulbous root of the hair is connected with
the papilla. In the cat the tactile nasal hairs are very large. Small bundles of
involuntary muscular fibres connect the corium with the root, so that in
contracting they elevate or expand the hair.
1. Single Hair-root and Shaft; 2. Vertical section, showing fibrous character of the
hair together with colouring matter, external edges serrated; 3. Transverse section
of human hair, medullary substance, and central pith.
The root of the hair is seen to dilate that it may fit more firmly into the skin
hair-follicle. The latter consists of two coats, an outer and an inner,
continuous with the epidermis, and this is called the root sheath. The outer
portion consists of three layers, formed of connective tissue, blood-vessels,
and nerves. The inner, or epidermic, coat comes away when the hair is
pulled out, and hence is called the root sheath. This again is made up of two
layers, the outer of which corresponds with the horny layer, and is
composed of flattened cells. The bulbous root of the hair is connected with
the papilla. In the cat the tactile nasal hairs are very large. Small bundles of
involuntary muscular fibres connect the corium with the root, so that in
contracting they elevate or expand the hair.
Page 746
Fig. 433.
1. Jointed hairs of Indian bat; 2. Hair of flying-fox, showing imbricated scales; 3.
Hair of mouse, showing pigment layers; 4. Hair of a small beetle (Dermestes). ×
250.
The hair of the lower animals presents a diversity of structure, especially on
the outer surface, and with reference to the arrangement of the scales. The
hair of the Indian bat, for instance, consists of a shaft invested with erectile
scales, placed at regular intervals; these stand out from the shaft, as in Fig.
433, No. 1. This form of scale varies considerably in the different species of
these animals, and a portion of hair near the root is nearly divested of
scales. Many of the scales are not unlike those of certain of the insect tribe,
seen in that of Dermestes, No. 3, while the hair of the mouse has a series of
transverse imbricated scales arranged as tiles on a house, due to
accumulated pigment. Hairs taken from various animals form interesting
objects of study for the microscope, as already noticed. Other hairs are
shown in Fig. 434. No. 1 is a transverse section of a hair from the ant-eater;
1. Jointed hairs of Indian bat; 2. Hair of flying-fox, showing imbricated scales; 3.
Hair of mouse, showing pigment layers; 4. Hair of a small beetle (Dermestes). ×
250.
The hair of the lower animals presents a diversity of structure, especially on
the outer surface, and with reference to the arrangement of the scales. The
hair of the Indian bat, for instance, consists of a shaft invested with erectile
scales, placed at regular intervals; these stand out from the shaft, as in Fig.
433, No. 1. This form of scale varies considerably in the different species of
these animals, and a portion of hair near the root is nearly divested of
scales. Many of the scales are not unlike those of certain of the insect tribe,
seen in that of Dermestes, No. 3, while the hair of the mouse has a series of
transverse imbricated scales arranged as tiles on a house, due to
accumulated pigment. Hairs taken from various animals form interesting
objects of study for the microscope, as already noticed. Other hairs are
shown in Fig. 434. No. 1 is a transverse section of a hair from the ant-eater;
Page 747
the central part consists of air-cells, the outer of a granular pith. No. 2 is a
transverse section of hair of peccary, with a diversified arrangement of the
cortical envelope, sending outward a set of radial prolongations and air-
cells; this kind of structure is also found in the quills of the porcupine. No. 3
is a transverse section of a hair of the elephant, which shows a combination
of a number of tubes united together, somewhat resembling the arrangement
of the hoof-horn of some of the ruminants, and the denser horny growth on
the snout of the rhinoceros, No. 4. The curious modification of these horny
structures is seen in the horns of other animals, and which may be likened
to a bundle of hairs. On making a transverse section, as in Fig. 434, and
submitting it to polarised light, on rotating the analyser, the dark central
spot shown is replaced by a bright one with a play of colours due to the
interference of light (Plate VIII., No. 178). The scales of fish are also of
interest (Fig. 435). These have been shown to afford an unerring guide in
the classification of fishes and in the examination of their fossil remains. As
a class of objects for the microscope, they are found to be both curious and
beautiful. Plate VIII., No. 176, is a scale of the grayling, seen under
polarised light.
Fig. 434.
1. Hair of ant-eater; 2. Hair of peccary; 3. Hair of elephant; 4. Horn of Rhinoceros.
transverse section of hair of peccary, with a diversified arrangement of the
cortical envelope, sending outward a set of radial prolongations and air-
cells; this kind of structure is also found in the quills of the porcupine. No. 3
is a transverse section of a hair of the elephant, which shows a combination
of a number of tubes united together, somewhat resembling the arrangement
of the hoof-horn of some of the ruminants, and the denser horny growth on
the snout of the rhinoceros, No. 4. The curious modification of these horny
structures is seen in the horns of other animals, and which may be likened
to a bundle of hairs. On making a transverse section, as in Fig. 434, and
submitting it to polarised light, on rotating the analyser, the dark central
spot shown is replaced by a bright one with a play of colours due to the
interference of light (Plate VIII., No. 178). The scales of fish are also of
interest (Fig. 435). These have been shown to afford an unerring guide in
the classification of fishes and in the examination of their fossil remains. As
a class of objects for the microscope, they are found to be both curious and
beautiful. Plate VIII., No. 176, is a scale of the grayling, seen under
polarised light.
Fig. 434.
1. Hair of ant-eater; 2. Hair of peccary; 3. Hair of elephant; 4. Horn of Rhinoceros.
Page 748
Of the harder outgrowths of the dermal
structures, the teeth afford the chief example
among animals. The rough anatomy of the tooth
in mankind consists of a crown, that projects
from the gum; a root, or fangs, fixed in a socket
of the jawbone, and a short intermediary neck.
Each tooth is supplied with an artery and nerve,
and has a central cavity filled with a soft,
vascular, sensitive substance, the pulp. On
making a vertical section of a tooth, we recognise
the several structures in the order of, pulp, crusta,
petrosa, dentine, and enamel. A section through a
human molar tooth (shown in Fig. 436) will
convey some idea of the arrangement of the
denser structures referred to above.
Fig. 435.—Fish Scale (Sole).
Fig. 436.—Sections of Human Molar Tooth (magnified 50 diameters). 1. Vertical
section; 2. Horizontal section.
Blandin was the first to demonstrate that teeth are developed in the mucous
membrane, similar to that of hair and nails. Teeth are formed in grooves of
structures, the teeth afford the chief example
among animals. The rough anatomy of the tooth
in mankind consists of a crown, that projects
from the gum; a root, or fangs, fixed in a socket
of the jawbone, and a short intermediary neck.
Each tooth is supplied with an artery and nerve,
and has a central cavity filled with a soft,
vascular, sensitive substance, the pulp. On
making a vertical section of a tooth, we recognise
the several structures in the order of, pulp, crusta,
petrosa, dentine, and enamel. A section through a
human molar tooth (shown in Fig. 436) will
convey some idea of the arrangement of the
denser structures referred to above.
Fig. 435.—Fish Scale (Sole).
Fig. 436.—Sections of Human Molar Tooth (magnified 50 diameters). 1. Vertical
section; 2. Horizontal section.
Blandin was the first to demonstrate that teeth are developed in the mucous
membrane, similar to that of hair and nails. Teeth are formed in grooves of
Page 749
the mucous membrane, and subsequently converted into closed sacs by a
process of involution, and their final adhesion to the jaw is a later process.
It is very generally conceded that teeth belong to the muco-dermoid, and not
to the periosteal, series of tissues; that, instead of standing in close relation
to the endo-skeleton, they are part of the dermal or exo-skeleton; their true
analogues being the hair, and some other epidermic appendages. Huxley
proved that, although teeth are developed in two ways, they are mere
varieties of the usual mode in the animal kingdom. In the first, which is
typified by the mackerel and the frog, the pulp is never free, but from the
first is inclosed within the capsule, seeming to sink down as fast as it grows.
In the other, the pulp projects freely at one period above the surface of the
mucous membrane, becoming subsequently included within a capsule
formed by the involution of the latter; this occurs in the human subject. The
skate offers a sort of intermediate structure.
Fig. 437.
1. Section of a cusp of the posterior molar of a child. The inner outline represents it
before the addition of acetic acid—the outer afterwards, when Nasmyth’s
membrane g is seen raised up in folds; f. the enamel organ; c. the dentine; the
central portion being filled with pulp. 2. Edge of the pulp of a molar cusp, showing
the first rudiment of the dentine, commencing in a perfectly transparent layer
between the nuclei of the pulp and the membrana preformativa. 3. Nasmyth’s
membrane detached from the subjacent enamel by acetic acid. 4. Stellate-cells of
the enamel organ. 5. Tooth of frog, acted on by dilute hydrochloric acid, so as to
dissolve out the enamel and free Nasmyth’s membrane. The structure of the
process of involution, and their final adhesion to the jaw is a later process.
It is very generally conceded that teeth belong to the muco-dermoid, and not
to the periosteal, series of tissues; that, instead of standing in close relation
to the endo-skeleton, they are part of the dermal or exo-skeleton; their true
analogues being the hair, and some other epidermic appendages. Huxley
proved that, although teeth are developed in two ways, they are mere
varieties of the usual mode in the animal kingdom. In the first, which is
typified by the mackerel and the frog, the pulp is never free, but from the
first is inclosed within the capsule, seeming to sink down as fast as it grows.
In the other, the pulp projects freely at one period above the surface of the
mucous membrane, becoming subsequently included within a capsule
formed by the involution of the latter; this occurs in the human subject. The
skate offers a sort of intermediate structure.
Fig. 437.
1. Section of a cusp of the posterior molar of a child. The inner outline represents it
before the addition of acetic acid—the outer afterwards, when Nasmyth’s
membrane g is seen raised up in folds; f. the enamel organ; c. the dentine; the
central portion being filled with pulp. 2. Edge of the pulp of a molar cusp, showing
the first rudiment of the dentine, commencing in a perfectly transparent layer
between the nuclei of the pulp and the membrana preformativa. 3. Nasmyth’s
membrane detached from the subjacent enamel by acetic acid. 4. Stellate-cells of
the enamel organ. 5. Tooth of frog, acted on by dilute hydrochloric acid, so as to
dissolve out the enamel and free Nasmyth’s membrane. The structure of the
Page 750
dentine e is rendered indistinct. At the base, Nasmyth’s membrane is continued
over the bony substance at z, in which the nuclei of the lacunæ are visible. (After
Huxley.) 6. Decalcified tooth-structure; a. the dentine; b. enamel organ; c. enamel;
d. Nasmyth’s membrane.
The enamel forms a continuous layer, and invests the crown of the tooth; it
is thickest upon the masticating surface, and decreases towards the neck,
where it usually terminates. The external surface of the enamel appears
smooth, but is always marked by delicate elevations and transverse ridges,
and covered by a fine membrane (Nasmyth’s membrane), containing
calcareous matter. This membrane is separable after being subjected to
hydrochloric acid; it then appears like a network of areolar tissue, shown in
Fig. 438, No. 6; Huxley’s “calcified membrana,” which commence at the
pulp cavity, and pass up to the enamel.
Fig. 438.—Tooth Structure.
1. Longitudinal section of superior canine tooth, exhibiting general arrangement,
and contour markings, slightly magnified; 2 and 3. Portions from same, highly
magnified, showing the relative position of bone-cells, cementum at 2, dentine
fibres, and commencement of enamel at 3; 4. Dentine fibres decalcified; 5.
Nasmyth’s membrane separated and the calcareous matter dissolved out with dilute
acid; 6. Cells of the pulp lying between it and the ivory; 7. A transverse section of
enamel, showing the sheaths of fibres, contents removed, and magnified 300
diameters.
Czermak discovered that the curious appearances of globular conglomerate
formations in the substance of dentine depend on its mode of calcification
over the bony substance at z, in which the nuclei of the lacunæ are visible. (After
Huxley.) 6. Decalcified tooth-structure; a. the dentine; b. enamel organ; c. enamel;
d. Nasmyth’s membrane.
The enamel forms a continuous layer, and invests the crown of the tooth; it
is thickest upon the masticating surface, and decreases towards the neck,
where it usually terminates. The external surface of the enamel appears
smooth, but is always marked by delicate elevations and transverse ridges,
and covered by a fine membrane (Nasmyth’s membrane), containing
calcareous matter. This membrane is separable after being subjected to
hydrochloric acid; it then appears like a network of areolar tissue, shown in
Fig. 438, No. 6; Huxley’s “calcified membrana,” which commence at the
pulp cavity, and pass up to the enamel.
Fig. 438.—Tooth Structure.
1. Longitudinal section of superior canine tooth, exhibiting general arrangement,
and contour markings, slightly magnified; 2 and 3. Portions from same, highly
magnified, showing the relative position of bone-cells, cementum at 2, dentine
fibres, and commencement of enamel at 3; 4. Dentine fibres decalcified; 5.
Nasmyth’s membrane separated and the calcareous matter dissolved out with dilute
acid; 6. Cells of the pulp lying between it and the ivory; 7. A transverse section of
enamel, showing the sheaths of fibres, contents removed, and magnified 300
diameters.
Czermak discovered that the curious appearances of globular conglomerate
formations in the substance of dentine depend on its mode of calcification
Page 751
and the presence of earthy material; and he attributed the contour lines to
the same cause. Contour markings vary in intensity and number; they are
most abundant in the root, and most marked in the crown. Vertical sections
exhibit them the best; as Fig. 440, No. 1. In preparing a specimen, first
make the section accurately, then decalcify it by submersion in dilute
hydrochloric acid; dry it and mount in Canada balsam; place the specimen
in the hot chamber for some time to soak in the fluid resin before it cools.
The white opacity at the extremity of the contour markings gives the
appearance of rings to the tooth-fang.
“The tooth-substance appears,” says Czermak, “on its inner surface, not as a
symmetrical whole, but consisting of balls of various diameter, which are
fused together into a mass with one another in different degrees, and in
which the dentine tubes in contact with the germ cavity terminate. By
reflected light, dark-ground illumination, one perceives this stalactite-like
condition of the inner surface of the tooth-substance very distinctly, by
means of the varied illumination of the globular elevations, and by the
shadows which they cast.” To see this structure to advantage the preparation
should be made from a tooth root, the growth of which is not complete.
With such preparations, the ground-substance of the last formed layer of the
tooth-substance is seen to be, at least partly, in the form of globular masses,
fused together with those of the penultimate layers.
The cementum is the cortical layer of osseous tissue, forming an outer
coating to the fangs, which it sometimes cements together. Its internal
surface is intimately united with the dentine, and in many teeth it would
appear as if the earliest determined arrangement of the fibres of the dentine
started from the canaliculi, as they radiate from the lacunæ in the cement.
The inter-lacunar layer is often striated, and exhibits a laminated structure:
sometimes it appears as if Haversian canals were running in a perpendicular
direction to the pulp cavity. The canaliculi frequently run out into numerous
branches, connecting one with another, and anastomising with the ends of
the dentine fibres. The thick layers of cement which occur in old teeth show
immense quantities of aggregated lacunæ of an irregular and elongated
form.
the same cause. Contour markings vary in intensity and number; they are
most abundant in the root, and most marked in the crown. Vertical sections
exhibit them the best; as Fig. 440, No. 1. In preparing a specimen, first
make the section accurately, then decalcify it by submersion in dilute
hydrochloric acid; dry it and mount in Canada balsam; place the specimen
in the hot chamber for some time to soak in the fluid resin before it cools.
The white opacity at the extremity of the contour markings gives the
appearance of rings to the tooth-fang.
“The tooth-substance appears,” says Czermak, “on its inner surface, not as a
symmetrical whole, but consisting of balls of various diameter, which are
fused together into a mass with one another in different degrees, and in
which the dentine tubes in contact with the germ cavity terminate. By
reflected light, dark-ground illumination, one perceives this stalactite-like
condition of the inner surface of the tooth-substance very distinctly, by
means of the varied illumination of the globular elevations, and by the
shadows which they cast.” To see this structure to advantage the preparation
should be made from a tooth root, the growth of which is not complete.
With such preparations, the ground-substance of the last formed layer of the
tooth-substance is seen to be, at least partly, in the form of globular masses,
fused together with those of the penultimate layers.
The cementum is the cortical layer of osseous tissue, forming an outer
coating to the fangs, which it sometimes cements together. Its internal
surface is intimately united with the dentine, and in many teeth it would
appear as if the earliest determined arrangement of the fibres of the dentine
started from the canaliculi, as they radiate from the lacunæ in the cement.
The inter-lacunar layer is often striated, and exhibits a laminated structure:
sometimes it appears as if Haversian canals were running in a perpendicular
direction to the pulp cavity. The canaliculi frequently run out into numerous
branches, connecting one with another, and anastomising with the ends of
the dentine fibres. The thick layers of cement which occur in old teeth show
immense quantities of aggregated lacunæ of an irregular and elongated
form.
Page 752
Compact Tissues, Cartilage and
Bone.—Cartilage is a bluish or
yellowish-white, semi-
transparent, elastic substance,
without vessels or nerves, and
surrounded by a membrane,
termed pericondrium, of a dense
fibrous nature. That kind,
however, known as articular Fig. 439.—Transverse section of Tooth of Pristis,
cartilage, receives a layer of showing orifices of medullary canals, with
systems of radiating fibres (tubuli) analogous to
epithelium from the synovial the Haversian canals in true bone.
membrane, but this is confined to
marginal portions, in consequence of the central wear which occurs as soon
as the parts are subjected to friction, during the movement of the limbs.
Cartilage covers the ends of all bones in apposition to form joints, and thus
lessens the effects of concussion. Besides the ordinary kind of cartilage,
temporary and permanent, there are two modifications of the tissue,
confined to certain portions of the body: cellular cartilage, composed of
cells lying close together, in a mesh formed of fine fibres; and fibro-
cartilage, cells distributed in a matrix of fibrous tissue.
Examined with a low power, cartilage appears to be homogeneous in
structure, studded over with numerous round, oval, oblong, semilunar, and
irregular-shaped corpuscles, as seen in Plate XIX., No. 8, a vertical section
of animal cartilage, arranged in columns, and condensed at the lower
surface previous to its conversion into bone. The greater opacity of this
portion is owing to the increase of osseous fibres, and the multiplication of
oil globules, and the intercellular spaces becoming filled with vessels. No. 9
shows a small transverse section of the same, with a further change of the
cartilage cells at a into bone cells, and at b with the characteristic canaliculi
and lacunæ. No. 7 further shows a section of the large tendon fixed to the
back of the heel of the foot, near the juncture of the tendo-Archillis with the
cartilage. For the examination of these several changes a high power is
necessary, and for the purpose pieces taken from the ox may be easily
obtained from the butcher, and fine sections cut with a razor parallel to the
surface.
Bone.—Cartilage is a bluish or
yellowish-white, semi-
transparent, elastic substance,
without vessels or nerves, and
surrounded by a membrane,
termed pericondrium, of a dense
fibrous nature. That kind,
however, known as articular Fig. 439.—Transverse section of Tooth of Pristis,
cartilage, receives a layer of showing orifices of medullary canals, with
systems of radiating fibres (tubuli) analogous to
epithelium from the synovial the Haversian canals in true bone.
membrane, but this is confined to
marginal portions, in consequence of the central wear which occurs as soon
as the parts are subjected to friction, during the movement of the limbs.
Cartilage covers the ends of all bones in apposition to form joints, and thus
lessens the effects of concussion. Besides the ordinary kind of cartilage,
temporary and permanent, there are two modifications of the tissue,
confined to certain portions of the body: cellular cartilage, composed of
cells lying close together, in a mesh formed of fine fibres; and fibro-
cartilage, cells distributed in a matrix of fibrous tissue.
Examined with a low power, cartilage appears to be homogeneous in
structure, studded over with numerous round, oval, oblong, semilunar, and
irregular-shaped corpuscles, as seen in Plate XIX., No. 8, a vertical section
of animal cartilage, arranged in columns, and condensed at the lower
surface previous to its conversion into bone. The greater opacity of this
portion is owing to the increase of osseous fibres, and the multiplication of
oil globules, and the intercellular spaces becoming filled with vessels. No. 9
shows a small transverse section of the same, with a further change of the
cartilage cells at a into bone cells, and at b with the characteristic canaliculi
and lacunæ. No. 7 further shows a section of the large tendon fixed to the
back of the heel of the foot, near the juncture of the tendo-Archillis with the
cartilage. For the examination of these several changes a high power is
necessary, and for the purpose pieces taken from the ox may be easily
obtained from the butcher, and fine sections cut with a razor parallel to the
surface.
Page 753
Fig. 440.
1. Cartilage from a mouse’s ear closely resembling vegetable tissue ×200; 2.
Cartilage from rabbit’s ear, with nucleated cells embedded in matrix; 3. Cartilage
from the end of a human rib ×300.
The better specimens for microscopical examination are those taken from
very young animals, in whom the ossific process is still incomplete. In
order to examine cellular cartilage, the ear of the mouse should be taken
and just dried sufficiently to enable fine sections to be cut by the microtome
transversely (Fig. 440).
Cartilage forms the entire skeleton of a certain number of fishes, as the
skate, lamprey, ray, shark, &c., the cells of which are embedded in a matrix
of granular matter, which has been properly termed intercellular. The
nearest approach to ossification of cartilage in fishes is that of the cuttle-
fish; in this stellate cells are freely distributed, as shown in Fig. 441, No. 3.
1. Cartilage from a mouse’s ear closely resembling vegetable tissue ×200; 2.
Cartilage from rabbit’s ear, with nucleated cells embedded in matrix; 3. Cartilage
from the end of a human rib ×300.
The better specimens for microscopical examination are those taken from
very young animals, in whom the ossific process is still incomplete. In
order to examine cellular cartilage, the ear of the mouse should be taken
and just dried sufficiently to enable fine sections to be cut by the microtome
transversely (Fig. 440).
Cartilage forms the entire skeleton of a certain number of fishes, as the
skate, lamprey, ray, shark, &c., the cells of which are embedded in a matrix
of granular matter, which has been properly termed intercellular. The
nearest approach to ossification of cartilage in fishes is that of the cuttle-
fish; in this stellate cells are freely distributed, as shown in Fig. 441, No. 3.
Page 754
Fig. 441.
1. Cartilage from the head of the skate, cells filled with nuclei; 2. Cartilage from
frog, oblong cells with nuclei; 3. Cartilage from cuttle-fish, with stellate cells, ×
200.
White fibro-cartilage occurs between the bodies of the vertebræ as a
connecting medium. In this kind the cells are more widely distributed,
specimens of which may be taken from the central portion of an
interarticular disc of any animal. The oval or circular corpuscles will be
seen surrounded by an abundance of fibrous tissue.
An acquaintance with the degeneration of the textures with which we have
been dealing may be of service to the student, as he may, in the course of
his examination, meet with an abnormal condition altogether different to
those described. The process of degeneration is usually a slow one, except
in the case of fatty infiltration, an example of which is furnished by the fatty
degeneration of the liver in Strasburg geese. Muscular tissue is very prone
to fatty degeneration, and fatty heart is often met with. Calcareous
degeneration of the muscles, ligaments, and cartilages, as well as morbid
deposits, are not at all uncommon in these structures. In Plate XIX., No. 9, a
small section is given of an enchondroma, and in which the round or ovoid
cells of the cartilage are seen degenerated and converted into granular
masses of a calcareous nature. Fig. 442 is a somewhat more highly
magnified section of a calcareous or morbid growth, taken from a human
1. Cartilage from the head of the skate, cells filled with nuclei; 2. Cartilage from
frog, oblong cells with nuclei; 3. Cartilage from cuttle-fish, with stellate cells, ×
200.
White fibro-cartilage occurs between the bodies of the vertebræ as a
connecting medium. In this kind the cells are more widely distributed,
specimens of which may be taken from the central portion of an
interarticular disc of any animal. The oval or circular corpuscles will be
seen surrounded by an abundance of fibrous tissue.
An acquaintance with the degeneration of the textures with which we have
been dealing may be of service to the student, as he may, in the course of
his examination, meet with an abnormal condition altogether different to
those described. The process of degeneration is usually a slow one, except
in the case of fatty infiltration, an example of which is furnished by the fatty
degeneration of the liver in Strasburg geese. Muscular tissue is very prone
to fatty degeneration, and fatty heart is often met with. Calcareous
degeneration of the muscles, ligaments, and cartilages, as well as morbid
deposits, are not at all uncommon in these structures. In Plate XIX., No. 9, a
small section is given of an enchondroma, and in which the round or ovoid
cells of the cartilage are seen degenerated and converted into granular
masses of a calcareous nature. Fig. 442 is a somewhat more highly
magnified section of a calcareous or morbid growth, taken from a human
Page 755
subject in which a morbid growth was seen to be gradually destroying the
bone and cartilage cells.
Bone.—Bone is a hard
unyielding structure, and which
in the vertebrata forms the
skeleton of the adult. It is the
framework for the support of the
soft tissues of the body, and
forms various cavities for the
reception of important organs, as
the brain, spinal cord, eyes, heart
and lungs, and acts as levers for
the action of the muscles and
joints. The partial elasticity of
bone is seen in the ribs, and the
rebound when the skull is
dropped on the ground. Bone
consists of earthy and animal
Fig. 442.—Cartilage taken from a diseased finger, in matters intimately combined; the
which both cartilage and bone were in a state of
degeneration. removal of either, however, does
not destroy the form of the bone,
if the process of separation be carefully conducted. The earthy constituents
may all be dissolved out by hydrochloric acid, but the form of the bone is
preserved in its minute particular, and in this state sections may be cut for
microscopical examination. If allowed to become dry it shrivels, and
assumes the density of horn. The interior of a bone is of a spongy or
cancellated structure, particularly at the ends. The outer portion of the bone
is more dense than the internal part. The study of bone should commence
with sections of the softened structure. Directions for making sections of
bone are given in the chapter on Practical Microscopy.
PLATE XX
bone and cartilage cells.
Bone.—Bone is a hard
unyielding structure, and which
in the vertebrata forms the
skeleton of the adult. It is the
framework for the support of the
soft tissues of the body, and
forms various cavities for the
reception of important organs, as
the brain, spinal cord, eyes, heart
and lungs, and acts as levers for
the action of the muscles and
joints. The partial elasticity of
bone is seen in the ribs, and the
rebound when the skull is
dropped on the ground. Bone
consists of earthy and animal
Fig. 442.—Cartilage taken from a diseased finger, in matters intimately combined; the
which both cartilage and bone were in a state of
degeneration. removal of either, however, does
not destroy the form of the bone,
if the process of separation be carefully conducted. The earthy constituents
may all be dissolved out by hydrochloric acid, but the form of the bone is
preserved in its minute particular, and in this state sections may be cut for
microscopical examination. If allowed to become dry it shrivels, and
assumes the density of horn. The interior of a bone is of a spongy or
cancellated structure, particularly at the ends. The outer portion of the bone
is more dense than the internal part. The study of bone should commence
with sections of the softened structure. Directions for making sections of
bone are given in the chapter on Practical Microscopy.
PLATE XX
Page 756
VERTEBRATA, BONE STRUCTURE.
The intimate structure of bone will be studied in connection with Plate XX.
Two series of lamellæ may be demonstrated in bone after maceration in
acid, a larger system surrounding the medullary canal, and a smaller
surrounding the Haversian canals, both of which are seen in Nos. 1 and 2.
In macerating bones, the lamellæ of the layer concentric system may be
peeled off in layers; these are seen to be pierced with fine apertures, caused
by the canaliculi. In some parts larger apertures are seen through which
bundles of fibres pass, pinning, as it were, the several layers together; these
are the perforating fibres. The outermost of the layers, being near the
periosteum, the membrane covering the bone, are termed periosteal layers;
the innermost, being close to the canal, are called medullary layers. No. 1 is
a transverse section of a flat bone, the clavicle, and it shows the Haversian
The intimate structure of bone will be studied in connection with Plate XX.
Two series of lamellæ may be demonstrated in bone after maceration in
acid, a larger system surrounding the medullary canal, and a smaller
surrounding the Haversian canals, both of which are seen in Nos. 1 and 2.
In macerating bones, the lamellæ of the layer concentric system may be
peeled off in layers; these are seen to be pierced with fine apertures, caused
by the canaliculi. In some parts larger apertures are seen through which
bundles of fibres pass, pinning, as it were, the several layers together; these
are the perforating fibres. The outermost of the layers, being near the
periosteum, the membrane covering the bone, are termed periosteal layers;
the innermost, being close to the canal, are called medullary layers. No. 1 is
a transverse section of a flat bone, the clavicle, and it shows the Haversian
Page 757
canals, varying in size from 1⁄2000th to 1⁄200th of an inch in diameter, the
largest being near the medullary canal. In shape they are round, oval, or
oblong, according to the line of section. Each canal is surrounded by rings,
none of which are complete, and running one into the other at various parts.
Under a higher power, those irregular shaped bodies termed lacunæ, with
fine radiating fibres, are seen to be smaller canals, canaliculi.
By means of this complete and intricate distribution of the canals of the
Haversian system, the nutritive fluids pass into the most compact parts of
the osseous tissue. Longitudinal sections of the long bones show these
canals as continuous branching-out cells.
In many of the lower animals the bony structure differs from those of man,
as will be seen in Plate XX. No. 3 shows a transverse section of the femur,
or leg-bone of an ostrich, magnified ninety-five times, in which the
Haversian canals are much smaller and more numerous, and many of them
run in the transverse direction. No. 4, again, is a transverse section of the
humerus, or fore-arm bone of a turtle (Chelonia mydas). This exhibits traces
of Haversian canals, with a slight tendency to a concentric arrangement of
bone-cells around them, the bone-cells being large and numerous, and
occur, for the most part, in parallel rows. In No. 5, a horizontal section of
the lower jaw-bone of a conger-eel exhibits a single plane of bone-cells
arranged in parallel lines. There are no Haversian canals present, and when
this specimen is contrasted with that of No. 4, it will be noticed that the
canaliculi given off from each of the bone-cells of this fish are very few in
number in comparison with that of the reptile. No. 6 is a section of a portion
of the cranium of a siren (Siren lacertina), remarkable for the large size of
the bone-cells, and of the canaliculi, which are larger in this animal than in
any other yet examined; and as in the preceding specimen, no Haversian
canals are present. No. 7 is a section of bone taken from the exterior of the
shaft of the humerus of a Pterodactyle; this exhibits the elongated bone-
cells characteristic of the order Reptilia. No. 8 is a horizontal section of a
scale, or flattened spine, from the skin of a Trygon, or sting ray; this
exhibits large Haversian canals, with numerous wavy parallel tubes, like
those of dentine, communicating with them. This specimen shows, besides
wavy tubes, numerous bone-cells, whose canaliculi communicate with the
tubes, as in dentine.
largest being near the medullary canal. In shape they are round, oval, or
oblong, according to the line of section. Each canal is surrounded by rings,
none of which are complete, and running one into the other at various parts.
Under a higher power, those irregular shaped bodies termed lacunæ, with
fine radiating fibres, are seen to be smaller canals, canaliculi.
By means of this complete and intricate distribution of the canals of the
Haversian system, the nutritive fluids pass into the most compact parts of
the osseous tissue. Longitudinal sections of the long bones show these
canals as continuous branching-out cells.
In many of the lower animals the bony structure differs from those of man,
as will be seen in Plate XX. No. 3 shows a transverse section of the femur,
or leg-bone of an ostrich, magnified ninety-five times, in which the
Haversian canals are much smaller and more numerous, and many of them
run in the transverse direction. No. 4, again, is a transverse section of the
humerus, or fore-arm bone of a turtle (Chelonia mydas). This exhibits traces
of Haversian canals, with a slight tendency to a concentric arrangement of
bone-cells around them, the bone-cells being large and numerous, and
occur, for the most part, in parallel rows. In No. 5, a horizontal section of
the lower jaw-bone of a conger-eel exhibits a single plane of bone-cells
arranged in parallel lines. There are no Haversian canals present, and when
this specimen is contrasted with that of No. 4, it will be noticed that the
canaliculi given off from each of the bone-cells of this fish are very few in
number in comparison with that of the reptile. No. 6 is a section of a portion
of the cranium of a siren (Siren lacertina), remarkable for the large size of
the bone-cells, and of the canaliculi, which are larger in this animal than in
any other yet examined; and as in the preceding specimen, no Haversian
canals are present. No. 7 is a section of bone taken from the exterior of the
shaft of the humerus of a Pterodactyle; this exhibits the elongated bone-
cells characteristic of the order Reptilia. No. 8 is a horizontal section of a
scale, or flattened spine, from the skin of a Trygon, or sting ray; this
exhibits large Haversian canals, with numerous wavy parallel tubes, like
those of dentine, communicating with them. This specimen shows, besides
wavy tubes, numerous bone-cells, whose canaliculi communicate with the
tubes, as in dentine.
Page 758
The following points may be noted with regard to the several sections of
bone described. That of the bird, for instance, contrasted with that of the
mammal, exhibits the following peculiarities: the Haversian canals are more
abundant, much smaller, and often run in a direction at right angles to that
of the shaft, by which means the concentric laminated arrangement is in
some cases lost; the direction of the canals follows the curve of the bone;
the bone-cells are much smaller and more numerous; while the number of
canaliculi sent off from the cells is less than in those of mammals. No. 3 is
the average length of a bone-cell of the ostrich, 1⁄2000th of an inch, in breadth
1⁄6000th.
In the Reptilia, the bones may be either hollow, cancellated, or solid; and
their specific gravity is less than that of birds or mammals. The short bones
of most of the chelonian reptiles are solid, and the long bones are either
hollow or cancellated; the ribs of the serpent-tribe are hollow, the medullary
cavity performing the office of a Haversian canal; the bone-cells are
accordingly arranged in concentric circles around their canals. The vertebræ
of these animals are solid; and the bone, like that of certain birds, is
remarkable for density and whiteness. When a transverse section is taken
from one of the long bones, and contrasted with that of a mammal or bird,
the difference will be noticed; there are very few, if any, Haversian canals,
and these are large; and at one view, in the section, No. 7, the canals and
bone-cells are arranged both vertically and longitudinally. The bone-cells
are remarkable for the great size to which they attain; in the turtle they are
1⁄375th of an inch in length, the canaliculi are extremely numerous, and are of
a size proportionate to that of the bone-cell.
In fishes a greater variation occurs in the minute structure of the skeleton
than in either of the three preceding classes. A rare structure is that of the
sword of the sword-fish (Istiophorus). In this, Haversian canals and a
concentric laminated arrangement of the bone are found, but no bone-cells.
The Haversian canals, when they are present, are of large size, and very
numerous, and then the bone-cells are, generally speaking, either absent or
but few in number, their place being occupied by tubes or canaliculi, which
are often of a very large size. The bone-cells are remarkable for their
graduate figure, and the canaliculi derived from them are comparatively few
in number. In a thin section of the scale of an osseous fish, the cells lie
bone described. That of the bird, for instance, contrasted with that of the
mammal, exhibits the following peculiarities: the Haversian canals are more
abundant, much smaller, and often run in a direction at right angles to that
of the shaft, by which means the concentric laminated arrangement is in
some cases lost; the direction of the canals follows the curve of the bone;
the bone-cells are much smaller and more numerous; while the number of
canaliculi sent off from the cells is less than in those of mammals. No. 3 is
the average length of a bone-cell of the ostrich, 1⁄2000th of an inch, in breadth
1⁄6000th.
In the Reptilia, the bones may be either hollow, cancellated, or solid; and
their specific gravity is less than that of birds or mammals. The short bones
of most of the chelonian reptiles are solid, and the long bones are either
hollow or cancellated; the ribs of the serpent-tribe are hollow, the medullary
cavity performing the office of a Haversian canal; the bone-cells are
accordingly arranged in concentric circles around their canals. The vertebræ
of these animals are solid; and the bone, like that of certain birds, is
remarkable for density and whiteness. When a transverse section is taken
from one of the long bones, and contrasted with that of a mammal or bird,
the difference will be noticed; there are very few, if any, Haversian canals,
and these are large; and at one view, in the section, No. 7, the canals and
bone-cells are arranged both vertically and longitudinally. The bone-cells
are remarkable for the great size to which they attain; in the turtle they are
1⁄375th of an inch in length, the canaliculi are extremely numerous, and are of
a size proportionate to that of the bone-cell.
In fishes a greater variation occurs in the minute structure of the skeleton
than in either of the three preceding classes. A rare structure is that of the
sword of the sword-fish (Istiophorus). In this, Haversian canals and a
concentric laminated arrangement of the bone are found, but no bone-cells.
The Haversian canals, when they are present, are of large size, and very
numerous, and then the bone-cells are, generally speaking, either absent or
but few in number, their place being occupied by tubes or canaliculi, which
are often of a very large size. The bone-cells are remarkable for their
graduate figure, and the canaliculi derived from them are comparatively few
in number. In a thin section of the scale of an osseous fish, the cells lie
Page 759
nearly all in one plane, and the anastomoses of the canaliculi are more
distinctly seen; in the hard scales of many, as the Lepidosteus and
Calicthys, and in spines of the Siluridæ, the bone-cells are well
differentiated. In the true bony scales comprising the exo-skeleton of
cartilaginous fishes the bone-cells are seen in great numbers.
Now, if we proceed at once to the application of the facts which have been
laid down, and make a fragment of bone of an extinct animal the subject of
investigation, it will be found that the bone-cells in Mammalia are tolerably
uniform in size; and if we take 1⁄2000th of an inch as a standard, the bone-
cells of birds fall below that standard; but the bone-cells of reptiles are
much above either of the two preceding, while those of fishes are
essentially different, both in size and shape, and are not likely to be
mistaken for one or the other; so that the determination of a minute yet
characteristic fragment of fishes’ bone is a task easily performed. If the
portion of bone does not exhibit bone-cells, but presents either one or other
of the characters indicated, the task of discrimination is equally easy. We
have now the mammal, the bird, and the reptile to deal with. In
consequence of the very great size of the cells and their canaliculi in the
reptile, a portion of bone of one of these animals can readily be
distinguished from that of a bird, or a mammal. The only difficulty lies
between these two last; but, notwithstanding that on a cursory glance the
bone of a bird appears very like that of a mammal, there are certain points
in their minute structure in which they differ; and one is the difference in
size of the bone-cells. To determine accurately, therefore, between the two,
we must, if the section be a transverse one, also note the comparative sizes
of the Haversian canals, and the tortuosity of their course; for the diameter
of the canal bears a certain proportion to the size of the bone-cells, and after
close examination the eye will readily detect differences.
distinctly seen; in the hard scales of many, as the Lepidosteus and
Calicthys, and in spines of the Siluridæ, the bone-cells are well
differentiated. In the true bony scales comprising the exo-skeleton of
cartilaginous fishes the bone-cells are seen in great numbers.
Now, if we proceed at once to the application of the facts which have been
laid down, and make a fragment of bone of an extinct animal the subject of
investigation, it will be found that the bone-cells in Mammalia are tolerably
uniform in size; and if we take 1⁄2000th of an inch as a standard, the bone-
cells of birds fall below that standard; but the bone-cells of reptiles are
much above either of the two preceding, while those of fishes are
essentially different, both in size and shape, and are not likely to be
mistaken for one or the other; so that the determination of a minute yet
characteristic fragment of fishes’ bone is a task easily performed. If the
portion of bone does not exhibit bone-cells, but presents either one or other
of the characters indicated, the task of discrimination is equally easy. We
have now the mammal, the bird, and the reptile to deal with. In
consequence of the very great size of the cells and their canaliculi in the
reptile, a portion of bone of one of these animals can readily be
distinguished from that of a bird, or a mammal. The only difficulty lies
between these two last; but, notwithstanding that on a cursory glance the
bone of a bird appears very like that of a mammal, there are certain points
in their minute structure in which they differ; and one is the difference in
size of the bone-cells. To determine accurately, therefore, between the two,
we must, if the section be a transverse one, also note the comparative sizes
of the Haversian canals, and the tortuosity of their course; for the diameter
of the canal bears a certain proportion to the size of the bone-cells, and after
close examination the eye will readily detect differences.
Page 760
Fig. 443.
1. A portion of the web of frog’s foot, spread out and slightly magnified to show
distribution of blood-vessels; 2. Is a portion magnified 250 diameters to show the
ovoid form of the blood discs in a vessel, beneath which hexagonal nucleated
epithelium cells appear.
Arteries and Veins.—The circulation of the animal frame is maintained by
arteries, veins, and capillaries. The arteries are elastic and contractile tubes;
these convey the blood from the heart to the capillaries. The larger arteries
are exceedingly elastic, but feebly contractile on account of the muscular
tissue in their walls. The veins ramify throughout the body, are more
numerous than the arteries, and of greater capacity. They usually
accompany the arteries and correspond to them in structure, the larger veins
possessing semi-lunar valves; these project into their interiors, and thus
prevent the regurgitation of the blood. They have four coats, consisting of
areolar tissue, yellow fibres combined with muscular fibres, and white
fibrous tissue, two layers of yellow fibres arranged longitudinally, and a
single layer of epithelial cells. Intermediate between the arteries and veins
there are exceedingly fine tubes, termed capillaries, in which the arteries
terminate, and from which the veins arise. These are composed of a fine
1. A portion of the web of frog’s foot, spread out and slightly magnified to show
distribution of blood-vessels; 2. Is a portion magnified 250 diameters to show the
ovoid form of the blood discs in a vessel, beneath which hexagonal nucleated
epithelium cells appear.
Arteries and Veins.—The circulation of the animal frame is maintained by
arteries, veins, and capillaries. The arteries are elastic and contractile tubes;
these convey the blood from the heart to the capillaries. The larger arteries
are exceedingly elastic, but feebly contractile on account of the muscular
tissue in their walls. The veins ramify throughout the body, are more
numerous than the arteries, and of greater capacity. They usually
accompany the arteries and correspond to them in structure, the larger veins
possessing semi-lunar valves; these project into their interiors, and thus
prevent the regurgitation of the blood. They have four coats, consisting of
areolar tissue, yellow fibres combined with muscular fibres, and white
fibrous tissue, two layers of yellow fibres arranged longitudinally, and a
single layer of epithelial cells. Intermediate between the arteries and veins
there are exceedingly fine tubes, termed capillaries, in which the arteries
terminate, and from which the veins arise. These are composed of a fine
Page 761
homogeneous membrane, with here and there a nucleus. The capillary
circulation of the blood is readily seen in the tail of the newt and the foot of
the frog, Fig. 443.
A network of capillaries conveying blood
to the lungs, and ramifying throughout the
structure, is shown in Fig. 444, and in Plate
XIX., No. 6, the termination of a capillary
of a blood-vessel in the fat-cells of the
human body. Plate VII. illustrates the
distribution of the arteries and veins to
various parts of the animal body. This
coloured plate, however, is designed to
show the value of injected preparations in
the delineation of animal structures. By
thus artificially restoring the blood and
distending the tissues, a much better idea is
obtained of the relative condition of parts,
the appearance presented by the erectile
papillæ, &c. In the section of foot of mouse
(No. 149), the bone is seen surrounded by Fig. 444.—A network of capillaries.
its vascular supply, arterial and venous; in
No. 150, the papillæ of the tongue are distended and seen erect; in No. 152,
a vertical section of the fungi-form papillæ on the tongue of cat, with
capillary loops passing into them, is demonstrated; in No. 151, the vertical
section of brain of a rat, the vascular supply is shown; No. 153, the
malpighian tufts (circular bodies) and arteries ramifying about the structure;
in No. 154, the vertical section through the intestine of the rat, shows villi
(arteries and veins) surmounted by epithelium, and supported on a layer of
the mucous membrane; in No. 155, the vascular supply sent to the roots of
the whisker of the nose of the mouse; in No. 157, a tangential section cut
through the several textures, the sclerotic coat and retina of the eye of a cat
is clearly made out although not highly magnified; again, in No. 156, the
beautiful vascular arrangement of the internal gill of the tadpole could
scarcely be so strikingly illustrated in any other way; while in the central,
No. 158, the vascular system throughout the whole of the body of a fully
developed tadpole, with the way in which the blood is carried from the
circulation of the blood is readily seen in the tail of the newt and the foot of
the frog, Fig. 443.
A network of capillaries conveying blood
to the lungs, and ramifying throughout the
structure, is shown in Fig. 444, and in Plate
XIX., No. 6, the termination of a capillary
of a blood-vessel in the fat-cells of the
human body. Plate VII. illustrates the
distribution of the arteries and veins to
various parts of the animal body. This
coloured plate, however, is designed to
show the value of injected preparations in
the delineation of animal structures. By
thus artificially restoring the blood and
distending the tissues, a much better idea is
obtained of the relative condition of parts,
the appearance presented by the erectile
papillæ, &c. In the section of foot of mouse
(No. 149), the bone is seen surrounded by Fig. 444.—A network of capillaries.
its vascular supply, arterial and venous; in
No. 150, the papillæ of the tongue are distended and seen erect; in No. 152,
a vertical section of the fungi-form papillæ on the tongue of cat, with
capillary loops passing into them, is demonstrated; in No. 151, the vertical
section of brain of a rat, the vascular supply is shown; No. 153, the
malpighian tufts (circular bodies) and arteries ramifying about the structure;
in No. 154, the vertical section through the intestine of the rat, shows villi
(arteries and veins) surmounted by epithelium, and supported on a layer of
the mucous membrane; in No. 155, the vascular supply sent to the roots of
the whisker of the nose of the mouse; in No. 157, a tangential section cut
through the several textures, the sclerotic coat and retina of the eye of a cat
is clearly made out although not highly magnified; again, in No. 156, the
beautiful vascular arrangement of the internal gill of the tadpole could
scarcely be so strikingly illustrated in any other way; while in the central,
No. 158, the vascular system throughout the whole of the body of a fully
developed tadpole, with the way in which the blood is carried from the
Page 762
remotest part of the tail to the heart, and sent to the gills, the brain, &c., it is
quite unnecessary to enlarge upon. These are seen under a low power, but
for the purpose of studying the basement membrane, together with the
intimate association and termination of the nerves accompanying the
arteries and veins, it is absolutely necessary to resort to a staining process,
and cutting fine sections with the microtome. Small portions of a nerve may
be cut off with fine scissors, teased out with needles, and a drop of acetic
acid added to render the sheath more transparent; in a few seconds the
connective tissue corpuscles will be brought into view. For the
microscopical examination of nerve-fibrillæ take a small section from the
leg of a frog, and tease it out in blood serum or white of egg. In size the
fibrillæ vary, even in the same nerve, from the 1⁄12000th to the 1⁄1500th of an
inch in diameter.
Fig. 445.
To show the circulation of the blood in the frog’s foot, and without causing
the animal pain or much inconvenience, it is better to enclose it in a black
silk bag, and draw out the foot as shown at a a a, Fig. 445. The bag
provided should be from three to four inches in length, and two and a half
inches broad, shown at b b, having a piece of tape, c c, sewn to each side,
about midway between the mouth and the bottom, and the mouth itself
capable of being closed by a drawing-in string, d d. Into this bag the frog is
placed, and only the leg which is about to be examined kept outside; the
string d d must then be drawn sufficiently tight around the small part of the
quite unnecessary to enlarge upon. These are seen under a low power, but
for the purpose of studying the basement membrane, together with the
intimate association and termination of the nerves accompanying the
arteries and veins, it is absolutely necessary to resort to a staining process,
and cutting fine sections with the microtome. Small portions of a nerve may
be cut off with fine scissors, teased out with needles, and a drop of acetic
acid added to render the sheath more transparent; in a few seconds the
connective tissue corpuscles will be brought into view. For the
microscopical examination of nerve-fibrillæ take a small section from the
leg of a frog, and tease it out in blood serum or white of egg. In size the
fibrillæ vary, even in the same nerve, from the 1⁄12000th to the 1⁄1500th of an
inch in diameter.
Fig. 445.
To show the circulation of the blood in the frog’s foot, and without causing
the animal pain or much inconvenience, it is better to enclose it in a black
silk bag, and draw out the foot as shown at a a a, Fig. 445. The bag
provided should be from three to four inches in length, and two and a half
inches broad, shown at b b, having a piece of tape, c c, sewn to each side,
about midway between the mouth and the bottom, and the mouth itself
capable of being closed by a drawing-in string, d d. Into this bag the frog is
placed, and only the leg which is about to be examined kept outside; the
string d d must then be drawn sufficiently tight around the small part of the
Page 763
leg to prevent the foot from being pulled into the bag, but not to stop the
circulation; three short pieces of thread, f f f, are now passed around the
three principal toes; and the bag with the frog must be fastened to the plate
a a by means of the tapes c c. When this is accomplished, the threads f f f
are passed either through some of the holes in the edge of the plate, three of
which are shown at g g g, in order to keep the web open; or, what answers
better, in a series of pegs of the shape represented by h, each having a slit, i,
extending more than halfway down it; the threads are wound round these
two or three times, and then the end is secured by putting it into the slit i.
The plate is now ready to be adapted to the stage of the microscope: the
square opening over which the foot is secured must be brought over the
aperture in the stage through which the light passes from the mirror.
The tadpole circulation is readily seen by placing the creature on its back,
when we immediately observe the beating heart, a bulbous-looking cavity,
formed of delicate, transparent tissue, through which the blood alternately
enters by one orifice and leaves by a more distant exit. The heart, it will be
noticed, is enclosed within its pericardium, this being the more delicate part
of the creature’s organisation. The binocular microscope should be used for
viewing the circulation. Passing along the course of the great blood-vessels
to the right and left of the heart, the eye is arrested by a large oval body, of a
more complicated structure. This is the inner gill, formed of delicate,
transparent tissue, traversed by arteries, and a network of blood-vessels. It
is almost unnecessary to say the tadpole has a respiratory and circulatory
system resembling those of fishes.
In nearly all fish the heart has but two cavities, an auricle and ventricle; the
blood is returned by the veins to the auricle, passes into the ventricle, and is
then transmitted to the gills, where, being exposed to the air contained in
the water, it becomes deprived of carbonic acid, aerated, and rendered fit to
breathe. In the reptile we find a modification of plan. The heart has three
cavities, two auricles and one ventricle; by this contrivance there is a
perpetual mixture in the heart of the impure carbonized blood which has
already circulated through the body, and flows into the ventricle from the
right auricle, with the purer aerated blood returned from the lungs, which
flows at the same instant into the ventricle from the left auricle.
circulation; three short pieces of thread, f f f, are now passed around the
three principal toes; and the bag with the frog must be fastened to the plate
a a by means of the tapes c c. When this is accomplished, the threads f f f
are passed either through some of the holes in the edge of the plate, three of
which are shown at g g g, in order to keep the web open; or, what answers
better, in a series of pegs of the shape represented by h, each having a slit, i,
extending more than halfway down it; the threads are wound round these
two or three times, and then the end is secured by putting it into the slit i.
The plate is now ready to be adapted to the stage of the microscope: the
square opening over which the foot is secured must be brought over the
aperture in the stage through which the light passes from the mirror.
The tadpole circulation is readily seen by placing the creature on its back,
when we immediately observe the beating heart, a bulbous-looking cavity,
formed of delicate, transparent tissue, through which the blood alternately
enters by one orifice and leaves by a more distant exit. The heart, it will be
noticed, is enclosed within its pericardium, this being the more delicate part
of the creature’s organisation. The binocular microscope should be used for
viewing the circulation. Passing along the course of the great blood-vessels
to the right and left of the heart, the eye is arrested by a large oval body, of a
more complicated structure. This is the inner gill, formed of delicate,
transparent tissue, traversed by arteries, and a network of blood-vessels. It
is almost unnecessary to say the tadpole has a respiratory and circulatory
system resembling those of fishes.
In nearly all fish the heart has but two cavities, an auricle and ventricle; the
blood is returned by the veins to the auricle, passes into the ventricle, and is
then transmitted to the gills, where, being exposed to the air contained in
the water, it becomes deprived of carbonic acid, aerated, and rendered fit to
breathe. In the reptile we find a modification of plan. The heart has three
cavities, two auricles and one ventricle; by this contrivance there is a
perpetual mixture in the heart of the impure carbonized blood which has
already circulated through the body, and flows into the ventricle from the
right auricle, with the purer aerated blood returned from the lungs, which
flows at the same instant into the ventricle from the left auricle.
Page 764
For the purpose of subsequent observations the tadpole should be selected
at a period in which the skin is perfectly transparent, otherwise the
appearances already described of the form and situation of the heart, and the
three great arterial trunks (proceeding right and left), will not be clearly
made out. The anatomical arrangement of the vessels will be seen to be
closely connected with the corresponding gill, the upper one (the cephalic)
running along the upper edge of the gill, giving off, in its course, a branch
which ascends to the mouth, with its accompanying vein; this is termed the
labial artery and vein. The cephalic artery continues its course around the
gill, until it suddenly curves upwards and backwards, and reaches the upper
surface of the head, when it dips down between the eye and the brain.
It must not be supposed that this can be made out in the average tadpole, the
obstacle to which is the large coil of intestines, usually distended with dark-
coloured food. This must first be reduced by making your tadpole live on
plain water for some days. Plate VII., No. 158, affords a view of the vessels
obtained under the influence of low diet, and whereby we are enabled to
trace the course of the three large arteries. The third trunk, traversing the
lung, is seen to emerge from the lower edge and descend into the abdomen
to form the great abdominal aorta. A small half-starved tadpole shows the
heart beating and the blood circulating, but the latter is quite colourless, not
a single red globule visible anywhere. The heart is a colourless globe, the
gills two transparent ovals, and the intestines a colourless, transparent coil.
Through the empty coil the artery is seen on either side leaving the gills,
and converging towards the spine, and uniting to form the abdominal aorta,
the large central vessel coloured red in the figure. After the aorta has
supplied the abdominal viscera, a prolongation, or caudal artery is seen
descending to the tail, the all-important organ of locomotion in the tadpole.
This artery, entering the root of the tail, is imbedded deeply in the flesh,
whence it emerges, and then continues its course, closely accompanied by
the vein, to within a short distance of the extremity, where, being reduced to
a state of extreme fineness, it terminates in a capillary loop, composed of
the end of the artery and the beginning of the vein. The artery, in its course,
gives off branches continually to supply the neighbouring tissue. The blood-
current in the tail is often seen, even in the main artery or vein, to be
sluggish. This occurs independently of the heart, which will continue to
beat as usual; it happens, because the circulation in the tail depends very
at a period in which the skin is perfectly transparent, otherwise the
appearances already described of the form and situation of the heart, and the
three great arterial trunks (proceeding right and left), will not be clearly
made out. The anatomical arrangement of the vessels will be seen to be
closely connected with the corresponding gill, the upper one (the cephalic)
running along the upper edge of the gill, giving off, in its course, a branch
which ascends to the mouth, with its accompanying vein; this is termed the
labial artery and vein. The cephalic artery continues its course around the
gill, until it suddenly curves upwards and backwards, and reaches the upper
surface of the head, when it dips down between the eye and the brain.
It must not be supposed that this can be made out in the average tadpole, the
obstacle to which is the large coil of intestines, usually distended with dark-
coloured food. This must first be reduced by making your tadpole live on
plain water for some days. Plate VII., No. 158, affords a view of the vessels
obtained under the influence of low diet, and whereby we are enabled to
trace the course of the three large arteries. The third trunk, traversing the
lung, is seen to emerge from the lower edge and descend into the abdomen
to form the great abdominal aorta. A small half-starved tadpole shows the
heart beating and the blood circulating, but the latter is quite colourless, not
a single red globule visible anywhere. The heart is a colourless globe, the
gills two transparent ovals, and the intestines a colourless, transparent coil.
Through the empty coil the artery is seen on either side leaving the gills,
and converging towards the spine, and uniting to form the abdominal aorta,
the large central vessel coloured red in the figure. After the aorta has
supplied the abdominal viscera, a prolongation, or caudal artery is seen
descending to the tail, the all-important organ of locomotion in the tadpole.
This artery, entering the root of the tail, is imbedded deeply in the flesh,
whence it emerges, and then continues its course, closely accompanied by
the vein, to within a short distance of the extremity, where, being reduced to
a state of extreme fineness, it terminates in a capillary loop, composed of
the end of the artery and the beginning of the vein. The artery, in its course,
gives off branches continually to supply the neighbouring tissue. The blood-
current in the tail is often seen, even in the main artery or vein, to be
sluggish. This occurs independently of the heart, which will continue to
beat as usual; it happens, because the circulation in the tail depends very
Page 765
much on the motion of the organ. When this is suspended (as in the
confined tadpole under the microscope), the blood moves sluggishly, or
stops, till the tail regains its freedom and motion, when the activity of the
current is restored.
Having traced the arterial system which conveys the blood from the heart to
the extremities, we will now note its return by the veins back again to the
heart.
The caudal vein runs near the artery during the greater part of its course,
with its stream of blood towards the heart. This stream is swollen by
perpetual tributaries from numerous vessels. As the vein approaches the
root of the tail it is inclined towards the artery, and diverges from it at the
point of entering the abdomen. Here it approaches the kidneys and sends off
branches, while the main trunk continues its course onward; and, passing
upwards behind a coil of intestine, it approaches the liver, and runs in a
curved course along the margin of that organ. The blood is now seen to
enter the vena cava by several channels, that converge towards the great
vein as it passes in close proximity to the organ. Beyond the liver the vena
cava continues its course upwards and inwards to its termination in the
sinus venosus or rudimentary auricle of the heart. This termination is the
junction of not less than six distinct venous trunks, incessantly pouring their
blood into the heart. The circulation in the fringed lips forms a most
complicated network of vessels, out of which proceeds a vein
corresponding to the artery already traced. This descends in a direct course
till it joins the principal vein of the head, which corresponds to the jugular
in the mammalia.
Thus it will be seen the blood is driven by the heart into each inner gill
through three large blood-vessels, which arise directly from the truncus
arteriosus, and may be called the afferent vessels of the gill. In Plate VII.,
No. 156, an enlarged view of a gill is shown.
On closer examination “each internal gill or entire branchial organ is seen
to consist of cartilaginous arches, with a piece of additional framework of a
triangular form, stretching beyond the arches, composed of semi-
transparent, gelatinous-looking material. These form the framework of the
organ and support upon their upper surface the three rows of crests with
confined tadpole under the microscope), the blood moves sluggishly, or
stops, till the tail regains its freedom and motion, when the activity of the
current is restored.
Having traced the arterial system which conveys the blood from the heart to
the extremities, we will now note its return by the veins back again to the
heart.
The caudal vein runs near the artery during the greater part of its course,
with its stream of blood towards the heart. This stream is swollen by
perpetual tributaries from numerous vessels. As the vein approaches the
root of the tail it is inclined towards the artery, and diverges from it at the
point of entering the abdomen. Here it approaches the kidneys and sends off
branches, while the main trunk continues its course onward; and, passing
upwards behind a coil of intestine, it approaches the liver, and runs in a
curved course along the margin of that organ. The blood is now seen to
enter the vena cava by several channels, that converge towards the great
vein as it passes in close proximity to the organ. Beyond the liver the vena
cava continues its course upwards and inwards to its termination in the
sinus venosus or rudimentary auricle of the heart. This termination is the
junction of not less than six distinct venous trunks, incessantly pouring their
blood into the heart. The circulation in the fringed lips forms a most
complicated network of vessels, out of which proceeds a vein
corresponding to the artery already traced. This descends in a direct course
till it joins the principal vein of the head, which corresponds to the jugular
in the mammalia.
Thus it will be seen the blood is driven by the heart into each inner gill
through three large blood-vessels, which arise directly from the truncus
arteriosus, and may be called the afferent vessels of the gill. In Plate VII.,
No. 156, an enlarged view of a gill is shown.
On closer examination “each internal gill or entire branchial organ is seen
to consist of cartilaginous arches, with a piece of additional framework of a
triangular form, stretching beyond the arches, composed of semi-
transparent, gelatinous-looking material. These form the framework of the
organ and support upon their upper surface the three rows of crests with
Page 766
their vascular network, and the main arterial and venous trunks lying
parallel to and between them. The three systemic arteries arising, right and
left, from the truncus arteriosus, enter each gill on its cardiac side, and then
follow the course of the crests, lying in close proximity to them. The upper
of these branchial arteries runs alone on the outside of the upper crest, and
another branch leaving the trunk and passing into the network of the crest,
whence a returning vessel may be traced carrying back the blood across the
branchial artery, and to a vessel lying close to and taking the same course as
the artery itself. Carrying the eye along the latter vessel we find, at a short
distance from the first of these crest branches, a second, leaving the main
trunk and entering the crest, when a corresponding returning vessel conveys
the blood across the arterial trunk into the vessel lying beside it, as in the
former instance. A number of these branches may be traced from one crest
to the other. But it is now seen that the trunk from which these arterial
branches spring diminishes in size as it proceeds in its course (like the gill
artery in fishes), while the vessel running parallel to it and receiving the
stream as it returns from the crest enlarges to some extent. Thus, the artery
or afferent vessel which brings the blood to the gill is large at its entrance,
but gradually diminishes and dwindles to a point at the opposite end of the
crest; while the venous or efferent vessel, beginning as a mere radical,
gradually enlarges, and thus becomes the trunk that conveys the blood out
of the gill to its ultimate destination. This vessel is the upper branchial vein
so long as it remains in contact with the gill; subsequently it changes its
name on leaving the gill and as it passes upwards for distribution to the
head, when it is designated the cephalic artery. The middle branchial artery
and vein proceed in like manner in connection with the middle crest, and
the lower artery and vein in connection with the lower crest. The middle
and lower venous trunks, having reached the extremity of the crests, curve
downwards and inwards, and leave the gill. The former trunk, converging
towards the spine, meets its fellow, and with it forms the ventral aorta. The
latter gives origin to the pulmonary artery, and supplies also the
integuments of the neck. Curious and interesting is the final stage of the
metamorphosis, when the waning tadpole and incipient frog coexist, and are
actually seen together in the same subject. The dwindling gills and the
shrinking tail—the last remnants of the tadpole form—are yet seen, in
company with the coloured, spotted skin, the newly formed and slender
parallel to and between them. The three systemic arteries arising, right and
left, from the truncus arteriosus, enter each gill on its cardiac side, and then
follow the course of the crests, lying in close proximity to them. The upper
of these branchial arteries runs alone on the outside of the upper crest, and
another branch leaving the trunk and passing into the network of the crest,
whence a returning vessel may be traced carrying back the blood across the
branchial artery, and to a vessel lying close to and taking the same course as
the artery itself. Carrying the eye along the latter vessel we find, at a short
distance from the first of these crest branches, a second, leaving the main
trunk and entering the crest, when a corresponding returning vessel conveys
the blood across the arterial trunk into the vessel lying beside it, as in the
former instance. A number of these branches may be traced from one crest
to the other. But it is now seen that the trunk from which these arterial
branches spring diminishes in size as it proceeds in its course (like the gill
artery in fishes), while the vessel running parallel to it and receiving the
stream as it returns from the crest enlarges to some extent. Thus, the artery
or afferent vessel which brings the blood to the gill is large at its entrance,
but gradually diminishes and dwindles to a point at the opposite end of the
crest; while the venous or efferent vessel, beginning as a mere radical,
gradually enlarges, and thus becomes the trunk that conveys the blood out
of the gill to its ultimate destination. This vessel is the upper branchial vein
so long as it remains in contact with the gill; subsequently it changes its
name on leaving the gill and as it passes upwards for distribution to the
head, when it is designated the cephalic artery. The middle branchial artery
and vein proceed in like manner in connection with the middle crest, and
the lower artery and vein in connection with the lower crest. The middle
and lower venous trunks, having reached the extremity of the crests, curve
downwards and inwards, and leave the gill. The former trunk, converging
towards the spine, meets its fellow, and with it forms the ventral aorta. The
latter gives origin to the pulmonary artery, and supplies also the
integuments of the neck. Curious and interesting is the final stage of the
metamorphosis, when the waning tadpole and incipient frog coexist, and are
actually seen together in the same subject. The dwindling gills and the
shrinking tail—the last remnants of the tadpole form—are yet seen, in
company with the coloured, spotted skin, the newly formed and slender
Page 767
legs, the flat head, the wide and toothless mouth, and the crouching attitude
of the all but perfect reptile.”87
To observe the circulation and how it is carried on during life in the gills,
the outer covering must be carefully raised, or even stripped off. This will
be better accomplished by putting the tadpole under the influence of
cocaine or chloroform—a drop of the fluid is sufficient for the purpose.
The metamorphosis in the embryo of the frog is by no means exceptional.
The ascidian begins life in the form of a tadpole, with a muscular tail;
subsequently it fixes itself by its head to a rock, and its tail disappears. The
changes the tadpole of the frog passes through are in every respect, except
in one or two minor details, similar to those of adult amphibia which pass
their whole lives in water. The newly-hatched flat-fish is symmetrical, an
eye being placed on each side of its head, with the adults of other fishes.
The fœtal whale has well-developed hind limbs, and which, after passing
into a condition almost perfect in proportion to the rest of the body,
gradually dwindle away again to the merest rudimentary structures. In all
these, and a number of similar cases, it is seen that the earlier condition of
existing animals represents, and is in agreement with that of its adult
ancestor of a remote period in the past. Collected facts bearing upon this
question have been made the groundwork of a theory of hereditary
properties in the germ, and a disposition to go through the same phases of
life as the parent.
of the all but perfect reptile.”87
To observe the circulation and how it is carried on during life in the gills,
the outer covering must be carefully raised, or even stripped off. This will
be better accomplished by putting the tadpole under the influence of
cocaine or chloroform—a drop of the fluid is sufficient for the purpose.
The metamorphosis in the embryo of the frog is by no means exceptional.
The ascidian begins life in the form of a tadpole, with a muscular tail;
subsequently it fixes itself by its head to a rock, and its tail disappears. The
changes the tadpole of the frog passes through are in every respect, except
in one or two minor details, similar to those of adult amphibia which pass
their whole lives in water. The newly-hatched flat-fish is symmetrical, an
eye being placed on each side of its head, with the adults of other fishes.
The fœtal whale has well-developed hind limbs, and which, after passing
into a condition almost perfect in proportion to the rest of the body,
gradually dwindle away again to the merest rudimentary structures. In all
these, and a number of similar cases, it is seen that the earlier condition of
existing animals represents, and is in agreement with that of its adult
ancestor of a remote period in the past. Collected facts bearing upon this
question have been made the groundwork of a theory of hereditary
properties in the germ, and a disposition to go through the same phases of
life as the parent.
Page 768
CHAPTER VI.
The Mineral and Geological Kingdoms.
The structure of rocks and the formation of crystals will be found to furnish
an endless supply of instructive material for the microscope. In sciences of
pure observation, as those of mineralogy and geology, the facts to be
observed are of several different kinds, and where so many observers are at
work all over the world, constant progress will necessarily be made, as well
as continued correction required from change and improvement in the
methods of observation. It would be impossible to give even a slight sketch
of what has been done in the two departments of nature referred to during
the past few years. Mineralogical and geological research have derived very
great advantage from having been assigned to professional teaching. But, as
Professor Bonney reminds us, the progress made in geological work in
particular, has been directly due to the revelations of the microscope. It
called forth an instrument of special construction for the purpose, the
petrological microscope (Fig. 79), well equipped with Nicol’s prisms, and
numerous other appliances demanded for the important investigations.
“Upon the history of the two main groups of rocks the microscope has
thrown much light. For the igneous rocks it has simplified their
classification and determined their mutual relations; while for the
rudimentary group, it has shown the true nature of their constituents, and
pointed out the sources from which they were derived. But it is in helping to
elucidate the problem of the metamorphic rocks, of which much less was
known, that the microscope has been of the most service. It has likewise
greatly assisted in the attempt to determine the history and mutual relation
of these rocks. One of the most important results within the last few years
has been the demonstration that without exception these crystallin schists
are very old, all probably older than the first rocks in which traces of life
have been found. The conclusion arrived at, is that “the environment
The Mineral and Geological Kingdoms.
The structure of rocks and the formation of crystals will be found to furnish
an endless supply of instructive material for the microscope. In sciences of
pure observation, as those of mineralogy and geology, the facts to be
observed are of several different kinds, and where so many observers are at
work all over the world, constant progress will necessarily be made, as well
as continued correction required from change and improvement in the
methods of observation. It would be impossible to give even a slight sketch
of what has been done in the two departments of nature referred to during
the past few years. Mineralogical and geological research have derived very
great advantage from having been assigned to professional teaching. But, as
Professor Bonney reminds us, the progress made in geological work in
particular, has been directly due to the revelations of the microscope. It
called forth an instrument of special construction for the purpose, the
petrological microscope (Fig. 79), well equipped with Nicol’s prisms, and
numerous other appliances demanded for the important investigations.
“Upon the history of the two main groups of rocks the microscope has
thrown much light. For the igneous rocks it has simplified their
classification and determined their mutual relations; while for the
rudimentary group, it has shown the true nature of their constituents, and
pointed out the sources from which they were derived. But it is in helping to
elucidate the problem of the metamorphic rocks, of which much less was
known, that the microscope has been of the most service. It has likewise
greatly assisted in the attempt to determine the history and mutual relation
of these rocks. One of the most important results within the last few years
has been the demonstration that without exception these crystallin schists
are very old, all probably older than the first rocks in which traces of life
have been found. The conclusion arrived at, is that “the environment
Page 769
necessary for changing an ordinary sediment into a crystalline schist existed
generally only in the earliest ages, and but very rarely and locally, if ever,
since palæozoic time began.”
The crystalline schists then are the relics still preserved to us of the early
days of the earth’s history, when the temperature near the surface was still
high. Since that time the zone for marked mineralogical changes has been
continually sinking, until at the present day it has reached a depth
practically unattainable. “The subterranean laboratory still exists, but the
way to it was virtually closed at a comparatively early period in the earth’s
history.” Greater progress has been made since the microscope was pressed
into the service of geology, and inspires the hope that we shall yet learn
something more of the earliest ages, when the mystery of life began.
“It may be regarded as one of the most remarkable results of geological
science, that an acquaintance with organic forms is at least as necessary for
a geologist as a knowledge of minerals, and that a correct knowledge of
organic remains (portions of fossil plants and animals) should prove a more
certain and unerring guide in unravelling the structure of complicated
districts of countries, than the most wide and general acquaintance with
inorganic substances. The cause of this, however, is obvious, as the mineral
substances produced at any one period of a vast succession of ages, do not
appear to have had any essential difference from those formed under like
circumstances at another. The animals and plants, however, living at one
period of the earth’s history were widely different from those living at other
periods. There has been a continuous succession of different races of living
beings on the earth following each other in a certain regular and
ascertainable order, and when that order has been determined, it is equally
certain that we can at once assign to its proper period of production, and
therefore to its proper place in the series of rocks, any portion of earthy
matter we may meet with containing any one, or even any recognisable
fragment of one, of these once living beings.”
The method of preparing sections of minerals and rocks for microscopic
examination will be found at pp. 241, 307-309. The sections, it is almost
needless to say, must be prepared thin enough to permit the use of
transmitted light, as well as for that of polarised light: that is to say, they
generally only in the earliest ages, and but very rarely and locally, if ever,
since palæozoic time began.”
The crystalline schists then are the relics still preserved to us of the early
days of the earth’s history, when the temperature near the surface was still
high. Since that time the zone for marked mineralogical changes has been
continually sinking, until at the present day it has reached a depth
practically unattainable. “The subterranean laboratory still exists, but the
way to it was virtually closed at a comparatively early period in the earth’s
history.” Greater progress has been made since the microscope was pressed
into the service of geology, and inspires the hope that we shall yet learn
something more of the earliest ages, when the mystery of life began.
“It may be regarded as one of the most remarkable results of geological
science, that an acquaintance with organic forms is at least as necessary for
a geologist as a knowledge of minerals, and that a correct knowledge of
organic remains (portions of fossil plants and animals) should prove a more
certain and unerring guide in unravelling the structure of complicated
districts of countries, than the most wide and general acquaintance with
inorganic substances. The cause of this, however, is obvious, as the mineral
substances produced at any one period of a vast succession of ages, do not
appear to have had any essential difference from those formed under like
circumstances at another. The animals and plants, however, living at one
period of the earth’s history were widely different from those living at other
periods. There has been a continuous succession of different races of living
beings on the earth following each other in a certain regular and
ascertainable order, and when that order has been determined, it is equally
certain that we can at once assign to its proper period of production, and
therefore to its proper place in the series of rocks, any portion of earthy
matter we may meet with containing any one, or even any recognisable
fragment of one, of these once living beings.”
The method of preparing sections of minerals and rocks for microscopic
examination will be found at pp. 241, 307-309. The sections, it is almost
needless to say, must be prepared thin enough to permit the use of
transmitted light, as well as for that of polarised light: that is to say, they
Page 770
should range from about 1⁄100th to 1⁄1000th of an inch. Almost any lapidary will
cut sections of any choice specimen.88 The formation of crystals, and the
method of preparing them for examination, has also been fully explained in
the chapter on polarised light, pp. 219 et seq., and illustrated on Plate VIII.
It is well known in micro-chemistry that “almost every substance, simple or
compound, capable of existing in the solid state, assumes, under favourable
conditions, a distinct geometrical figure, usually bounded by plane surfaces
and having angles of constant value.
Much useful information may be gained upon micro-crystallography, as
well as on almost everything having any relation to the technique of the
microscope, in the “Journal of the Royal Microscopical Society.” To the
June number (1898) Mr. T. Charters White contributes an article on crystals,
and reminds us that the presence of much or little moisture will modify and
alter forms, as much and as often as varying degrees of temperature. At the
same time he offers a few useful suggestions for the purpose of securing
better results, for which purpose he employs hippuric acid, hydroquinine,
and picric acid alone or in combination with hippuric acid, and an aqueous
solution of bichromate of potassium, crystallised in a tolerably thick
emulsion of gum arabic. This is the only aqueous solution; the other
solvents have been methylated spirit, acetone, and absolute alcohol, taking
these three solvents as types of the greatest volatility, because in making
certain crystals it is necessary that the solvent should evaporate quickly,
otherwise the crystals will assume their original forms. It is further
desirable to make saturated, or even super-saturated solutions of the three
chemicals named, as the colours produced under polarised light are of a
deeper and richer character than they are if made from weaker solutions. Of
the three chemicals named he prefers hippuric acid, for reasons stated, that
it is the most manageable, and allows of more time being taken in
modifying the formation of the crystals. It is also advisable to slightly warm
the glass slide before the drop of fluid is applied. On the whole, picric acid
appears to furnish a greater variety of crystals when used in combination
with bichromate of potassium and a solution of gum arabic.
cut sections of any choice specimen.88 The formation of crystals, and the
method of preparing them for examination, has also been fully explained in
the chapter on polarised light, pp. 219 et seq., and illustrated on Plate VIII.
It is well known in micro-chemistry that “almost every substance, simple or
compound, capable of existing in the solid state, assumes, under favourable
conditions, a distinct geometrical figure, usually bounded by plane surfaces
and having angles of constant value.
Much useful information may be gained upon micro-crystallography, as
well as on almost everything having any relation to the technique of the
microscope, in the “Journal of the Royal Microscopical Society.” To the
June number (1898) Mr. T. Charters White contributes an article on crystals,
and reminds us that the presence of much or little moisture will modify and
alter forms, as much and as often as varying degrees of temperature. At the
same time he offers a few useful suggestions for the purpose of securing
better results, for which purpose he employs hippuric acid, hydroquinine,
and picric acid alone or in combination with hippuric acid, and an aqueous
solution of bichromate of potassium, crystallised in a tolerably thick
emulsion of gum arabic. This is the only aqueous solution; the other
solvents have been methylated spirit, acetone, and absolute alcohol, taking
these three solvents as types of the greatest volatility, because in making
certain crystals it is necessary that the solvent should evaporate quickly,
otherwise the crystals will assume their original forms. It is further
desirable to make saturated, or even super-saturated solutions of the three
chemicals named, as the colours produced under polarised light are of a
deeper and richer character than they are if made from weaker solutions. Of
the three chemicals named he prefers hippuric acid, for reasons stated, that
it is the most manageable, and allows of more time being taken in
modifying the formation of the crystals. It is also advisable to slightly warm
the glass slide before the drop of fluid is applied. On the whole, picric acid
appears to furnish a greater variety of crystals when used in combination
with bichromate of potassium and a solution of gum arabic.
Page 771
APPENDICES AND TABLES USEFUL TO THE
MICROSCOPIST.
Appendix A.
ILLUMINATION ARRANGEMENTS OF THE MICROSCOPE.
A doubt has of late been expressed among practical microscopists as to the
value of the illumination arrangements of the lamp and the microscope, so
as to secure the more perfect definition of the flagellate organ of the monas
and other minute forms of infusorial life. We have been told that better
results will be obtained by turning the mirror aside, and so disposing the
microscope and lamp in the horizontal position, that the central rays of light
from the mirror-edge of the lamp-flame shall pass through the optical axis
of the achromatic condenser, the focus of which must be accurately brought
upon the field of view by means of the substage centring screws and rack-
work, and in such a manner, that by employing a 1-inch objective, a
sharply-defined image of the lamp-flame, edge-on, is projected on to the
centre of the field in association with the specimen under examination. If
the 1-inch objective be now replaced by a 1-12th or 1-16th inch immersion
and once again focussed into place, and a slight re-adjustment of the
centring made, it will be found that the field is brilliantly illuminated, and
the most minute portions of infusorial life are well defined, and with a
sharpness otherwise unattainable. At the same time the graduating or iris
diaphragm must be brought into use.
Dr. Clifford Mercer, the President of the American Microscopical Society,
who has quite recently reinvestigated the question of illumination, utterly
condemns the narrow cone, as well as that of oblique light in all such
investigations, and considers the 3-4ths axil cone as the most suitable
method for microscopical illumination, and he bases his resolving limit
MICROSCOPIST.
Appendix A.
ILLUMINATION ARRANGEMENTS OF THE MICROSCOPE.
A doubt has of late been expressed among practical microscopists as to the
value of the illumination arrangements of the lamp and the microscope, so
as to secure the more perfect definition of the flagellate organ of the monas
and other minute forms of infusorial life. We have been told that better
results will be obtained by turning the mirror aside, and so disposing the
microscope and lamp in the horizontal position, that the central rays of light
from the mirror-edge of the lamp-flame shall pass through the optical axis
of the achromatic condenser, the focus of which must be accurately brought
upon the field of view by means of the substage centring screws and rack-
work, and in such a manner, that by employing a 1-inch objective, a
sharply-defined image of the lamp-flame, edge-on, is projected on to the
centre of the field in association with the specimen under examination. If
the 1-inch objective be now replaced by a 1-12th or 1-16th inch immersion
and once again focussed into place, and a slight re-adjustment of the
centring made, it will be found that the field is brilliantly illuminated, and
the most minute portions of infusorial life are well defined, and with a
sharpness otherwise unattainable. At the same time the graduating or iris
diaphragm must be brought into use.
Dr. Clifford Mercer, the President of the American Microscopical Society,
who has quite recently reinvestigated the question of illumination, utterly
condemns the narrow cone, as well as that of oblique light in all such
investigations, and considers the 3-4ths axil cone as the most suitable
method for microscopical illumination, and he bases his resolving limit
Page 772
accordingly. Some important experiments are brought forward by Dr.
Mercer, which at the same time demonstrate the correctness of Lord
Rayleigh’s limit of resolution (referred to in a previous chapter, p. 44), for
circular apertures as contrasted with that calculated by the late Sir George
Airy.
With regard to the Abbé Theory, Dr. Mercer says: “Resolution in the Abbé
Theory may be said to increase by bounds. So long as the central image of
the source of light alone is to be seen at the back of the objective, resolution
is not present. The aperture may be increased without change in the
contraction of the diffraction pattern, and in accompanying resolution, so
long as the central image alone is to be seen at the back of the objective; but
the moment the increase in aperture is sufficient to uncover or admit one
flanking spectrum image, resolution is present. With greater increase in
aperture, no improvement in the picture as to the contraction of the
diffraction pattern is to be seen until another spectrum image is uncovered
or admitted. Dr. Mercer gives his reasons for considering that the
advantageous reduction in a cone of light between an object and the
objective should not exceed, in the case of first-class objectives, one-fourth
to one-third (never more than one-half) of the diameter of the cone. On the
other hand, with full cone illumination, resolution increases continuously,
and not by jumps or by periodic accessions. With regard to the use of
oblique light, he says his Photos 2, 3, and 489 are a pictorial warning for a
second time against the use of oblique illumination in ordinary work us a
means of increasing, or of attempting to exhaust the resolving power of the
microscope. At the same time it becomes evident that every substage should
be provided with a means by which its condenser may be accurately
centred, and that every student using the microscope should be familiar
with a method of centring his substage condenser.
Dr. Mercer summarises the results of his experiments thus:—
1. “Diffraction rays on leaving an object may be considered in the same
category with other rays changed in direction by an object.
2. “The diffraction phenomena seen in a projected image are essentially the
effect of changes in light above the objective, due to a function of aperture,
Mercer, which at the same time demonstrate the correctness of Lord
Rayleigh’s limit of resolution (referred to in a previous chapter, p. 44), for
circular apertures as contrasted with that calculated by the late Sir George
Airy.
With regard to the Abbé Theory, Dr. Mercer says: “Resolution in the Abbé
Theory may be said to increase by bounds. So long as the central image of
the source of light alone is to be seen at the back of the objective, resolution
is not present. The aperture may be increased without change in the
contraction of the diffraction pattern, and in accompanying resolution, so
long as the central image alone is to be seen at the back of the objective; but
the moment the increase in aperture is sufficient to uncover or admit one
flanking spectrum image, resolution is present. With greater increase in
aperture, no improvement in the picture as to the contraction of the
diffraction pattern is to be seen until another spectrum image is uncovered
or admitted. Dr. Mercer gives his reasons for considering that the
advantageous reduction in a cone of light between an object and the
objective should not exceed, in the case of first-class objectives, one-fourth
to one-third (never more than one-half) of the diameter of the cone. On the
other hand, with full cone illumination, resolution increases continuously,
and not by jumps or by periodic accessions. With regard to the use of
oblique light, he says his Photos 2, 3, and 489 are a pictorial warning for a
second time against the use of oblique illumination in ordinary work us a
means of increasing, or of attempting to exhaust the resolving power of the
microscope. At the same time it becomes evident that every substage should
be provided with a means by which its condenser may be accurately
centred, and that every student using the microscope should be familiar
with a method of centring his substage condenser.
Dr. Mercer summarises the results of his experiments thus:—
1. “Diffraction rays on leaving an object may be considered in the same
category with other rays changed in direction by an object.
2. “The diffraction phenomena seen in a projected image are essentially the
effect of changes in light above the objective, due to a function of aperture,
Page 773
and not to changes below the objective, due to diffraction of light in the
plane of the object.
3. “Diffraction in the plane of the object does, under some circumstances,
furnish light to certain parts of an aperture from which primary rays are
absent, and this enables aperture to more fully determine the character of
the projected image, resulting in a more nearly truthful image, or, on the
other hand, in false appearances. This is the gist of the Abbé phenomena of
microscopic vision.
4. “But such phenomena are not peculiar to microscopic vision,
notwithstanding Professor Abbé’s claim to the contrary.
5. “With any positive lens similar and more brilliant results may be got by
utilising corresponding pencils of primary rays, instead of isolated pencils
of diffracted rays.
6. “Still more trustworthy results may be got by using primary rays in place
of the isolated pencils of primary rays.
7. “An advantage peculiar to using narrow cone illumination with an
objective of wide aperture (the only illumination admissible in the Abbé
theory), consists in giving, under suitable conditions, approximately the
acme of resolving power simultaneously in each several diameters. Thus a
circular aperture is approximately squared or made rectangular as to
resolving power in several of its diameters simultaneously.
8. “Special attention is called to the fact that the Abbé theory deals with
complex objects; for only such objects are subject to resolution. Single
particles and uniform areas are outside its domain. These latter, however,
are microscopic objects, and all objects are essentially different shaped
aggregations of points. An isolated point-like particle, no matter what its
minuteness, may be seen if it present sufficient contrast with the
surrounding microscopic field. The size of the disc image is no less than a
limit determined finally by aperture. That limit in size varying inversely
with aperture, determines the limit of resolving power. This is the gist of the
theory of microscopic vision which harmonises with our experimental study
of aperture.”
plane of the object.
3. “Diffraction in the plane of the object does, under some circumstances,
furnish light to certain parts of an aperture from which primary rays are
absent, and this enables aperture to more fully determine the character of
the projected image, resulting in a more nearly truthful image, or, on the
other hand, in false appearances. This is the gist of the Abbé phenomena of
microscopic vision.
4. “But such phenomena are not peculiar to microscopic vision,
notwithstanding Professor Abbé’s claim to the contrary.
5. “With any positive lens similar and more brilliant results may be got by
utilising corresponding pencils of primary rays, instead of isolated pencils
of diffracted rays.
6. “Still more trustworthy results may be got by using primary rays in place
of the isolated pencils of primary rays.
7. “An advantage peculiar to using narrow cone illumination with an
objective of wide aperture (the only illumination admissible in the Abbé
theory), consists in giving, under suitable conditions, approximately the
acme of resolving power simultaneously in each several diameters. Thus a
circular aperture is approximately squared or made rectangular as to
resolving power in several of its diameters simultaneously.
8. “Special attention is called to the fact that the Abbé theory deals with
complex objects; for only such objects are subject to resolution. Single
particles and uniform areas are outside its domain. These latter, however,
are microscopic objects, and all objects are essentially different shaped
aggregations of points. An isolated point-like particle, no matter what its
minuteness, may be seen if it present sufficient contrast with the
surrounding microscopic field. The size of the disc image is no less than a
limit determined finally by aperture. That limit in size varying inversely
with aperture, determines the limit of resolving power. This is the gist of the
theory of microscopic vision which harmonises with our experimental study
of aperture.”
Page 774
Appendix B.
MICRO-PHOTOGRAPHY.
Owing in some measure to the more complete knowledge of the subject
gained by the experience of years, and the extreme value of micro-
photography in the delineation of bacteria, and perhaps in a measure to the
advent of the perfected dry-plate process, photography is being rapidly
pressed forward in conjunction with the microscope. In the course of the
year [1898] no less than six, more or less, new forms of micro-photographic
apparatus have appeared; two are simple, one for daylight, one for lamp,
one for electric, and one for lime-light illumination. Passing over the
simpler forms, for a notice of which I am unable to find room, there is one
piece of new apparatus, that of Mr. E. B. Stringer, which is not only new,
but is in every way adapted to the work of micro-photography. It is in fact a
well-arranged camera, fitted with a powerful condensing arrangement, each
portion of which is capable of being independently centred and controlled.
Indeed, the specially interesting feature of the apparatus is the control of the
gas and the beautiful and uniformally illuminating disc of zircon, about a
quarter of an inch in diameter.
Fig. 446.—Mr. E. B. Stringer’s Improved Micro-photography Apparatus.
B. Oxyhydrogen jet with zirconium cylinder, covered by the cowl A when
working.
C. Doublet parallelising condenser, with centering screws.
D. Iris diaphragm.
E. Holder for trough and light-filtering media.
F. Plano-convex lens, 41⁄4ins. diameter, with centering screws G
H. Plano-concave lens, with iris diaphragm T.
K. Connecting pulleys between focussing rod of camera and fine adjustment of
Microscope.
L. Triangular frame in which Microscope feet are placed.
M. Flap shutter.
MICRO-PHOTOGRAPHY.
Owing in some measure to the more complete knowledge of the subject
gained by the experience of years, and the extreme value of micro-
photography in the delineation of bacteria, and perhaps in a measure to the
advent of the perfected dry-plate process, photography is being rapidly
pressed forward in conjunction with the microscope. In the course of the
year [1898] no less than six, more or less, new forms of micro-photographic
apparatus have appeared; two are simple, one for daylight, one for lamp,
one for electric, and one for lime-light illumination. Passing over the
simpler forms, for a notice of which I am unable to find room, there is one
piece of new apparatus, that of Mr. E. B. Stringer, which is not only new,
but is in every way adapted to the work of micro-photography. It is in fact a
well-arranged camera, fitted with a powerful condensing arrangement, each
portion of which is capable of being independently centred and controlled.
Indeed, the specially interesting feature of the apparatus is the control of the
gas and the beautiful and uniformally illuminating disc of zircon, about a
quarter of an inch in diameter.
Fig. 446.—Mr. E. B. Stringer’s Improved Micro-photography Apparatus.
B. Oxyhydrogen jet with zirconium cylinder, covered by the cowl A when
working.
C. Doublet parallelising condenser, with centering screws.
D. Iris diaphragm.
E. Holder for trough and light-filtering media.
F. Plano-convex lens, 41⁄4ins. diameter, with centering screws G
H. Plano-concave lens, with iris diaphragm T.
K. Connecting pulleys between focussing rod of camera and fine adjustment of
Microscope.
L. Triangular frame in which Microscope feet are placed.
M. Flap shutter.
Page 775
N. Door through which image is observed on card screen, etc.
O. Solid block of mahogany on which camera body is fixed and supported.
P. Dark slide.
This efficient photo-micrographic apparatus (Fig. 446) is made by Messrs.
W. Watson & Sons, under the instructions of Mr. E. B. Stringer. The
illuminating condensing system is mounted on a square brass bar, the
illuminant being oxygen-hydrogen light burning on zirconium. Immediately
in front of this is a condenser, c, four and a half inches diameter, with an iris
diaphragm, D, immediately in front of it. The holder, E, carries the light
filtering media through which the beam passes and enters the condenser, F.
It then goes through a tank of water contained in the cone, F to H, and
emerges a practically parallel beam of great intensity through a plano-
concave lens, h, of such a diameter as to exactly fill the back lens of the
substage condenser. There is an iris diaphragm, T, for cutting off stray light.
The whole of the apparatus is fitted with centring screws and clamps, and
after having been once adjusted it is ready for use at any moment without
preparation. By means of this apparatus, instantaneous pictures can be taken
of living rotifers, so brilliant is the illumination, while photographs of such
fine objects as the flagella of bacteria cannot be secured with the same
amount of certainty by any other microphotographic apparatus with which I
have made myself acquainted.
Appendix C.
FORMULÆ AND METHODS:—CEMENTING,
CLEARING, HARDENING AND MOUNTING.90
CLEARING AGENTS.
The object of employing a clearing agent is to replace the alcohol in the
dehydrated section by a liquid which has a refractive index about the same
as the balsam into which it is to be placed, and which will readily mix with
it.
O. Solid block of mahogany on which camera body is fixed and supported.
P. Dark slide.
This efficient photo-micrographic apparatus (Fig. 446) is made by Messrs.
W. Watson & Sons, under the instructions of Mr. E. B. Stringer. The
illuminating condensing system is mounted on a square brass bar, the
illuminant being oxygen-hydrogen light burning on zirconium. Immediately
in front of this is a condenser, c, four and a half inches diameter, with an iris
diaphragm, D, immediately in front of it. The holder, E, carries the light
filtering media through which the beam passes and enters the condenser, F.
It then goes through a tank of water contained in the cone, F to H, and
emerges a practically parallel beam of great intensity through a plano-
concave lens, h, of such a diameter as to exactly fill the back lens of the
substage condenser. There is an iris diaphragm, T, for cutting off stray light.
The whole of the apparatus is fitted with centring screws and clamps, and
after having been once adjusted it is ready for use at any moment without
preparation. By means of this apparatus, instantaneous pictures can be taken
of living rotifers, so brilliant is the illumination, while photographs of such
fine objects as the flagella of bacteria cannot be secured with the same
amount of certainty by any other microphotographic apparatus with which I
have made myself acquainted.
Appendix C.
FORMULÆ AND METHODS:—CEMENTING,
CLEARING, HARDENING AND MOUNTING.90
CLEARING AGENTS.
The object of employing a clearing agent is to replace the alcohol in the
dehydrated section by a liquid which has a refractive index about the same
as the balsam into which it is to be placed, and which will readily mix with
it.
Page 776
Oil of Bergamot will clear quickly from 90 per cent. of alcohol. Clove oil
clears more rapidly, but it dissolves out aniline colours to a considerable
extent. Xylol is without action on aniline colours. This strength of alcohol is
chosen because of its being that of the methylated spirit sold in London, and
which is much used in washing and dehydrating on account of its
cheapness.
Oil of Cedar Wood, although an essential oil, resembles xylol, but
evaporates slowly. It has very little solvent action on the aniline colours. It
clears rapidly from absolute alcohol, but not well from 90 per cent. Sections
can be left in it for several days. It is a convenient medium in which to
examine tissues before mounting them permanently. It clears celloidin
without dissolving it; and as a connecting fluid between the object and
objective nothing better has been discovered.
Other clearing agents have been tried, but as they dissolve out the aniline
colours, are no longer used.
CEMENTS.
Grove’s Mastic and Bismuth.—Dissolve gum mastic in chloroform, and
thicken with nitrate of bismuth. The solution of mastic should be nearly
saturated.
Grove’s Oxide of Zinc, Dammar, and Drying Oil.—Rub up well-ground
oxide of zinc, 2 ozs., with drying oil, to the consistence of thick paint. Then
add an equal quantity of gum dammar, previously dissolved in benzoline,
and of the thickness of syrup. Strain through close-meshed muslin. Keep in
well-corked bottle, and, if necessary, thin with benzoline.
Isinglass Cement.—Heat the isinglass in a covered vessel on the water-bath
with a little glacial acetic acid, until it is thoroughly softened and forms a
stiff mass, then gradually add more acid until it produces a thick solution
which is of uniform consistence, and just fluid while hot. Then run into
wide-mouth bottles and close with good corks.
clears more rapidly, but it dissolves out aniline colours to a considerable
extent. Xylol is without action on aniline colours. This strength of alcohol is
chosen because of its being that of the methylated spirit sold in London, and
which is much used in washing and dehydrating on account of its
cheapness.
Oil of Cedar Wood, although an essential oil, resembles xylol, but
evaporates slowly. It has very little solvent action on the aniline colours. It
clears rapidly from absolute alcohol, but not well from 90 per cent. Sections
can be left in it for several days. It is a convenient medium in which to
examine tissues before mounting them permanently. It clears celloidin
without dissolving it; and as a connecting fluid between the object and
objective nothing better has been discovered.
Other clearing agents have been tried, but as they dissolve out the aniline
colours, are no longer used.
CEMENTS.
Grove’s Mastic and Bismuth.—Dissolve gum mastic in chloroform, and
thicken with nitrate of bismuth. The solution of mastic should be nearly
saturated.
Grove’s Oxide of Zinc, Dammar, and Drying Oil.—Rub up well-ground
oxide of zinc, 2 ozs., with drying oil, to the consistence of thick paint. Then
add an equal quantity of gum dammar, previously dissolved in benzoline,
and of the thickness of syrup. Strain through close-meshed muslin. Keep in
well-corked bottle, and, if necessary, thin with benzoline.
Isinglass Cement.—Heat the isinglass in a covered vessel on the water-bath
with a little glacial acetic acid, until it is thoroughly softened and forms a
stiff mass, then gradually add more acid until it produces a thick solution
which is of uniform consistence, and just fluid while hot. Then run into
wide-mouth bottles and close with good corks.
Page 777
Kitton’s Cement of white lead and red lead in powder, and litharge powder
in equal parts. Grind together with a little turpentine, until thoroughly
incorporated, and mix with gold size. The mixture should be thin enough to
use with a brush; in using, one coat should be allowed to dry before
applying another. No more cement should be mixed with the gold size than
is required for immediate use, as it sets quickly, and becomes unworkable.
Krönig’s Cement.—Gradually add ordinary resin, 7 to 9 parts, to melted
beeswax, 2 parts, then steam and cool.
Shellac Cement.—Dissolve shellac in an equal weight of methylated spirit,
then pour off the clear portion and add a few drops of balsam and castor oil.
Marine Glue.—Dissolve indiarubber in mineral naphtha, and add twice the
quantity of powdered shellac; or make chloroform the solvent, and use
mastic instead of shellac. For casting battery trays, use a composition of 4
parts resin and 1 of gutta percha, with a little boiled oil.
Selier (Cleaning Glass Slides).—New slides or cover-glasses must be
placed for a few hours in a mixture of 1 part of potassium bichromate, 1 of
sulphuric acid, and 25 of water. Subsequently wash with water and wipe dry
with a linen rag, after draining off the excess of moisture. Covers that have
been used should be previously immersed for a few days in a mixture of
equal parts of alcohol and hydrochloric acid. Scrape old slides free of
mounting medium before immersing them in the bichromate solution.
Elsching’s Celloidin Solution.—Allow the celloidin shavings to swell up
for 24 hours in the necessary quantity of absolute alcohol, then add the
proper amount of ether.
Koch’s Copal.—Stain small pieces of material in bulk, and dehydrate with
alcohol, then immerse in a thin solution of copal in chloroform. Evaporate
with a gentle heat until the solution is so far concentrated as to draw out
into threads that are brittle on cooling. Then remove the objects and leave
on a tile for a few days to dry. Sections may then be cut by means of a fine
saw. If objects are imbedded unstained, remove copal from sections by
soaking in chloroform, decalcify if necessary, and stain.
in equal parts. Grind together with a little turpentine, until thoroughly
incorporated, and mix with gold size. The mixture should be thin enough to
use with a brush; in using, one coat should be allowed to dry before
applying another. No more cement should be mixed with the gold size than
is required for immediate use, as it sets quickly, and becomes unworkable.
Krönig’s Cement.—Gradually add ordinary resin, 7 to 9 parts, to melted
beeswax, 2 parts, then steam and cool.
Shellac Cement.—Dissolve shellac in an equal weight of methylated spirit,
then pour off the clear portion and add a few drops of balsam and castor oil.
Marine Glue.—Dissolve indiarubber in mineral naphtha, and add twice the
quantity of powdered shellac; or make chloroform the solvent, and use
mastic instead of shellac. For casting battery trays, use a composition of 4
parts resin and 1 of gutta percha, with a little boiled oil.
Selier (Cleaning Glass Slides).—New slides or cover-glasses must be
placed for a few hours in a mixture of 1 part of potassium bichromate, 1 of
sulphuric acid, and 25 of water. Subsequently wash with water and wipe dry
with a linen rag, after draining off the excess of moisture. Covers that have
been used should be previously immersed for a few days in a mixture of
equal parts of alcohol and hydrochloric acid. Scrape old slides free of
mounting medium before immersing them in the bichromate solution.
Elsching’s Celloidin Solution.—Allow the celloidin shavings to swell up
for 24 hours in the necessary quantity of absolute alcohol, then add the
proper amount of ether.
Koch’s Copal.—Stain small pieces of material in bulk, and dehydrate with
alcohol, then immerse in a thin solution of copal in chloroform. Evaporate
with a gentle heat until the solution is so far concentrated as to draw out
into threads that are brittle on cooling. Then remove the objects and leave
on a tile for a few days to dry. Sections may then be cut by means of a fine
saw. If objects are imbedded unstained, remove copal from sections by
soaking in chloroform, decalcify if necessary, and stain.
Page 778
Eulenstein’s Cement.—Mix equal parts of Brunswick black and gold size
with a very little Canada balsam.
DECALCIFYING AND BLEACHING.
In the case of bony structures, or tissues so impregnated with calcium salts,
the material should be decalcified by an acid capable of dissolving out the
mineral matter. Hydrochloric acid with alcohol is in more general use. The
older the bone the stronger will be the acid required, nitric with alcohol and
chromic acid. Picric acid is preferred for fœtal bone.
Andeer, J. J., finds an aqueous solution of phloroglucin acts as a powerful
decalcifying agent on the bones of animals, but is without action on the
most delicate organic tissue. If treatment with hydrochloric acid be
employed as well, the residual “ossein” will be without a trace of either
calcium phosphate or carbonate.
Ebner’s Fluids.—(1) Mix 100 C.c. of cold saturated aqueous solution of
sodium chloride, 100 C.c. of water, and 4 C.c. of hydrochloric acid.
Preparations are placed in the fluid, and 1 to 2 C.c. of hydrochloric acid
added daily until they are soft. (2) Mix 2·5 parts of hydrochloric acid (sp.
gr. 1·16) with 500 of alcohol (90 per cent.), 100 of water, and 2·5 of sodium
chloride.
Fol’s Liquid.—Mix 70 volumes of 1 per cent. chromic acid, 3 of nitric acid,
and 200 of water.
Mayer’s Desilification Process.—Place the objects in alcohol contained in
a glass vessel coated internally with paraffin, then add hydrofluoric acid
drop by drop until desilification is complete, avoiding the fumes
meanwhile.
Marsh’s Chlorine Method.—Chlorine is generated in a small bottle by
treating crystals of potassium chlorate with strong HCl., and the gas is led
through a piece of glass tubing, bent twice at right angles, to the bottom of a
bottle containing the sections immersed in water.
with a very little Canada balsam.
DECALCIFYING AND BLEACHING.
In the case of bony structures, or tissues so impregnated with calcium salts,
the material should be decalcified by an acid capable of dissolving out the
mineral matter. Hydrochloric acid with alcohol is in more general use. The
older the bone the stronger will be the acid required, nitric with alcohol and
chromic acid. Picric acid is preferred for fœtal bone.
Andeer, J. J., finds an aqueous solution of phloroglucin acts as a powerful
decalcifying agent on the bones of animals, but is without action on the
most delicate organic tissue. If treatment with hydrochloric acid be
employed as well, the residual “ossein” will be without a trace of either
calcium phosphate or carbonate.
Ebner’s Fluids.—(1) Mix 100 C.c. of cold saturated aqueous solution of
sodium chloride, 100 C.c. of water, and 4 C.c. of hydrochloric acid.
Preparations are placed in the fluid, and 1 to 2 C.c. of hydrochloric acid
added daily until they are soft. (2) Mix 2·5 parts of hydrochloric acid (sp.
gr. 1·16) with 500 of alcohol (90 per cent.), 100 of water, and 2·5 of sodium
chloride.
Fol’s Liquid.—Mix 70 volumes of 1 per cent. chromic acid, 3 of nitric acid,
and 200 of water.
Mayer’s Desilification Process.—Place the objects in alcohol contained in
a glass vessel coated internally with paraffin, then add hydrofluoric acid
drop by drop until desilification is complete, avoiding the fumes
meanwhile.
Marsh’s Chlorine Method.—Chlorine is generated in a small bottle by
treating crystals of potassium chlorate with strong HCl., and the gas is led
through a piece of glass tubing, bent twice at right angles, to the bottom of a
bottle containing the sections immersed in water.
Page 779
Ranvier’s Fluid.—Use 50 per cent. hydrochloric acid with the addition of
sodium chloride to counteract its swelling action.
Squire’s Fluid.—(1) Mix 95 parts of glycerine with 5 parts of hydrochloric
acid; used for softening teeth. (2) Use a 4 per cent. aqueous solution of
arsenic acid at a temperature of 30° to 40° C. After softening tissues in this
solution, keep them in alcohol.
Waldeyer.—To a 0·1 per cent. solution of palladium chloride, add one-
tenth its volume of hydrochloric acid.
HARDENING, FREEZING, AND EMBEDDING.
Altmann (Fixing Solution).—A mixture of equal parts of 5 per cent.
potassium bichromate solution and 2 per cent. osmic acid.
Alcohol.—Strengths of alcoholic solutions, as given by Squire, will be
found of practical value. Absolute alcohol (sp. gr. O·797) containing about
98 per cent. of ethylic alcohol is taken as the basis in most instances.
Alcohol of 90 per cent. (sp. gr. 0·823) is prepared by mixing 14 volumes of
absolute alcohol and 1 volume of distilled water; 84 per cent. alcohol (sp.
gr. 0·838) is rectified spirit B.P.; 70 per cent. alcohol (sp. gr. 0·872) may be
obtained by adding 1 volume of distilled water to 3 volumes of absolute
alcohol, 6 volumes of rectified spirit, or 4 volumes of methylated spirit; 50
per cent. alcohol (sp. gr. 0·918) is prepared by adding 4 volumes of distilled
water to 5 volumes of absolute alcohol, 3 volumes of water to 5 volumes of
rectified spirit, or 3·5 volumes of water to 5 volumes of methylated spirit.
Absolute alcohol, 75 C.c., mixed with acetic acid, 25 C.c., serves as an
excellent fixing agent for nuclei. Immerse tissues in it for 6 to 12 hours,
then transfer to 90 per cent. alcohol until hardened, afterwards preserving in
70 per cent. alcohol till wanted.
Betz’s Hardening Fluid.—A mixture of equal parts of sulphuric ether and
alcohol. This is used for hardening the brain of insects prior to cutting
sections.
sodium chloride to counteract its swelling action.
Squire’s Fluid.—(1) Mix 95 parts of glycerine with 5 parts of hydrochloric
acid; used for softening teeth. (2) Use a 4 per cent. aqueous solution of
arsenic acid at a temperature of 30° to 40° C. After softening tissues in this
solution, keep them in alcohol.
Waldeyer.—To a 0·1 per cent. solution of palladium chloride, add one-
tenth its volume of hydrochloric acid.
HARDENING, FREEZING, AND EMBEDDING.
Altmann (Fixing Solution).—A mixture of equal parts of 5 per cent.
potassium bichromate solution and 2 per cent. osmic acid.
Alcohol.—Strengths of alcoholic solutions, as given by Squire, will be
found of practical value. Absolute alcohol (sp. gr. O·797) containing about
98 per cent. of ethylic alcohol is taken as the basis in most instances.
Alcohol of 90 per cent. (sp. gr. 0·823) is prepared by mixing 14 volumes of
absolute alcohol and 1 volume of distilled water; 84 per cent. alcohol (sp.
gr. 0·838) is rectified spirit B.P.; 70 per cent. alcohol (sp. gr. 0·872) may be
obtained by adding 1 volume of distilled water to 3 volumes of absolute
alcohol, 6 volumes of rectified spirit, or 4 volumes of methylated spirit; 50
per cent. alcohol (sp. gr. 0·918) is prepared by adding 4 volumes of distilled
water to 5 volumes of absolute alcohol, 3 volumes of water to 5 volumes of
rectified spirit, or 3·5 volumes of water to 5 volumes of methylated spirit.
Absolute alcohol, 75 C.c., mixed with acetic acid, 25 C.c., serves as an
excellent fixing agent for nuclei. Immerse tissues in it for 6 to 12 hours,
then transfer to 90 per cent. alcohol until hardened, afterwards preserving in
70 per cent. alcohol till wanted.
Betz’s Hardening Fluid.—A mixture of equal parts of sulphuric ether and
alcohol. This is used for hardening the brain of insects prior to cutting
sections.
Page 780
Cole’s Freezing Process.—Dissolve picked gum acacia, 4 ozs., in distilled
water, 6 ozs., and to each 5 parts of the resulting mucilage add 3 parts of
syrup made by dissolving loaf sugar, 1 lb., in distilled water, 1 pint. To each
ounce of the medium add 5 grains of pure carbolic acid, and soak the tissues
in it prior to freezing. For tissues liable to come to pieces, mix 4 parts of
syrup with 5 of mucilage.
Flemming’s Fixing Solution.—Osmic acid (1 per cent. solution), 80 C.c.;
chromic acid (10 per cent. solution), 15 C.c.; glacial acetic acid, 10 C.c.;
distilled water, 95 C.c.
Fol’s Fixing—Osmic acid (1 per cent. solution), 4 C.c.; chromic acid (10
per cent. solution), 5 C.c.; glacial acetic acid, 10 C.c.; distilled water, 181
C.c.
Fischer’s Imbedding Mass.—Dissolve 15 parts of transparent soap in 17·5
parts of 96 per cent. alcohol.
Klein’s Hardening.—Mix 1 C.c. of 10 per cent. chromic acid solution with
60 C.c. of water, and add 30 C.c. of 90 per cent. alcohol.
Müller’s Fluid Formula, see page 288.—This solution is sometimes
mixed with one-third its volume of 90 per cent. alcohol, its hardening action
being then much more rapid.
Rabl’s Hardening Fluid.—Chromic acid solution (10 per cent.), 7 C.c.;
water, 200 C.c.; formic acid (sp. gr. 1·2), 5 drops.
Rollett’s Freezing Process.—Small portions of tissue placed on the stage
of microtome, after immersion in the white of an egg, then frozen and cut
with a very cold knife.
Ryder (Double Embedding).—After the celloidin bath, soak objects in
chloroform, then remove into a mixture of chloroform and paraffin, heated
to not more than 40° C., and finally into a bath of pure paraffin.
Stricker (Imbedding Mass).—Prepare the objects in alcohol and imbed in a
concentrated solution in gum arabic in a paper case, then throw the whole
water, 6 ozs., and to each 5 parts of the resulting mucilage add 3 parts of
syrup made by dissolving loaf sugar, 1 lb., in distilled water, 1 pint. To each
ounce of the medium add 5 grains of pure carbolic acid, and soak the tissues
in it prior to freezing. For tissues liable to come to pieces, mix 4 parts of
syrup with 5 of mucilage.
Flemming’s Fixing Solution.—Osmic acid (1 per cent. solution), 80 C.c.;
chromic acid (10 per cent. solution), 15 C.c.; glacial acetic acid, 10 C.c.;
distilled water, 95 C.c.
Fol’s Fixing—Osmic acid (1 per cent. solution), 4 C.c.; chromic acid (10
per cent. solution), 5 C.c.; glacial acetic acid, 10 C.c.; distilled water, 181
C.c.
Fischer’s Imbedding Mass.—Dissolve 15 parts of transparent soap in 17·5
parts of 96 per cent. alcohol.
Klein’s Hardening.—Mix 1 C.c. of 10 per cent. chromic acid solution with
60 C.c. of water, and add 30 C.c. of 90 per cent. alcohol.
Müller’s Fluid Formula, see page 288.—This solution is sometimes
mixed with one-third its volume of 90 per cent. alcohol, its hardening action
being then much more rapid.
Rabl’s Hardening Fluid.—Chromic acid solution (10 per cent.), 7 C.c.;
water, 200 C.c.; formic acid (sp. gr. 1·2), 5 drops.
Rollett’s Freezing Process.—Small portions of tissue placed on the stage
of microtome, after immersion in the white of an egg, then frozen and cut
with a very cold knife.
Ryder (Double Embedding).—After the celloidin bath, soak objects in
chloroform, then remove into a mixture of chloroform and paraffin, heated
to not more than 40° C., and finally into a bath of pure paraffin.
Stricker (Imbedding Mass).—Prepare the objects in alcohol and imbed in a
concentrated solution in gum arabic in a paper case, then throw the whole
Page 781
into alcohol and cut after 2 or 3 days.
Webb (Dextrin Freezing).—A thick solution of dextrin (1:40) in aqueous
solution of carbolic acid is used for imbedding, and subsequently frozen.
MOUNTING MEDIA.
Sections are usually mounted in balsam, dammar, glycerine, &c., but it is
not a necessity that the cover-glass should be fixed or cemented down.
Some cements (caoutchouc by preference) should be employed when
glycerine or aqueous (Farrant’s) media are used.
Alleger’s Gelatine Process.—Add a few drops of formalin to each
gramme of 0·5 to 1 per cent. gelatine solution. After mounting the section in
this, apply heat to the slide until the paraffin is softened, and allow the
superfluous gelatine to drain from the edge of the slide.
Apáthy’s Mounting Medium.—Picked gum arabic, 50 Gm.; cane-sugar, 50
Gm.; distilled water, 50 Gm.; dissolve over a warm bath and add 0·05 Gm.
of thymol. This medium sets very hard, and combined with a paper cell it
may be used for ringing glycerine mounts.
Cole’s Slow or Exposure Method of Mounting.—Dissolve dried Canada
balsam, 3 ozs., in benzole, 3 fl. ozs., and filter. Apply a clean cover-glass to
a slide that has been moistened by breathing on it, and place a few drops of
the balsam solution on the cover-glass. Then remove a section from
turpentine, and put it into the balsam. Put aside for 12 hours to allow the
benzole to evaporate, and having warmed a slide and added a drop of fresh
balsam solution to that on the cover-glass, bring the fluid balsam in contact
with the warmed slide. Press the cover down carefully to avoid the
inclusion of air bubbles, and when the excess of balsam is squeezed out, put
the slide aside to cool, after which it may be cleaned with a camel-hair
brush or soft rag moistened with methylated spirit.
Farrant’s Solution.—Take of gum arabic 5 parts; water 5 parts; when the
gum is fairly dissolved add 10 parts of a 5 per cent. solution of carbolic
acid.
Webb (Dextrin Freezing).—A thick solution of dextrin (1:40) in aqueous
solution of carbolic acid is used for imbedding, and subsequently frozen.
MOUNTING MEDIA.
Sections are usually mounted in balsam, dammar, glycerine, &c., but it is
not a necessity that the cover-glass should be fixed or cemented down.
Some cements (caoutchouc by preference) should be employed when
glycerine or aqueous (Farrant’s) media are used.
Alleger’s Gelatine Process.—Add a few drops of formalin to each
gramme of 0·5 to 1 per cent. gelatine solution. After mounting the section in
this, apply heat to the slide until the paraffin is softened, and allow the
superfluous gelatine to drain from the edge of the slide.
Apáthy’s Mounting Medium.—Picked gum arabic, 50 Gm.; cane-sugar, 50
Gm.; distilled water, 50 Gm.; dissolve over a warm bath and add 0·05 Gm.
of thymol. This medium sets very hard, and combined with a paper cell it
may be used for ringing glycerine mounts.
Cole’s Slow or Exposure Method of Mounting.—Dissolve dried Canada
balsam, 3 ozs., in benzole, 3 fl. ozs., and filter. Apply a clean cover-glass to
a slide that has been moistened by breathing on it, and place a few drops of
the balsam solution on the cover-glass. Then remove a section from
turpentine, and put it into the balsam. Put aside for 12 hours to allow the
benzole to evaporate, and having warmed a slide and added a drop of fresh
balsam solution to that on the cover-glass, bring the fluid balsam in contact
with the warmed slide. Press the cover down carefully to avoid the
inclusion of air bubbles, and when the excess of balsam is squeezed out, put
the slide aside to cool, after which it may be cleaned with a camel-hair
brush or soft rag moistened with methylated spirit.
Farrant’s Solution.—Take of gum arabic 5 parts; water 5 parts; when the
gum is fairly dissolved add 10 parts of a 5 per cent. solution of carbolic
acid.
Page 782
Flemming’s Glycerine Preservative.—Mix equal parts of alcohol,
glycerine, and water. Lee recommends the addition of 0·5 to 0·75 per cent.
of acetic acid.
Lee’s Turpentine Colophonium Mounting Medium.—This is highly
recommended for general work, and is prepared by adding small pieces of
colophonium to rectified oil of turpentine, heating in a stove, and when the
solution is sufficiently thick filtering twice in the stove.
Seaman (Glycerine Jelly).—Dissolve isinglass in water so as to make a jelly
that remains stiff at the ordinary temperature of the room, and add one-tenth
part of glycerine, together with a little solution of borax, carbolic acid, or
camphor water. Filter through muslin whilst warm and add a little alcohol.
Seiler (Alcohol Balsam).—Heat Canada balsam until it becomes brittle
when cold, then dissolve in warm absolute alcohol and filter through
absorbent cotton-wool. This is chiefly useful as a mounting medium for
objects stained with carmine.
Squire (Farrant’s Medium).—Dissolve in 200 C.c. of distilled water 1 Gm.
of arsenious acid and 130 Gm. of gum arabic, then add 100 C.c. of
glycerine. Filter through fine Swedish filter paper upon which has been
deposited a thin layer of talc.
Squire (Glycerine and Gum).—Dissolve 130 Gm. of gum arabic in 200 C.c.
of chloroform water (1 in 200), then add 100 C.c. of glycerine and filter.
Squire (Glycerine Jelly).—Soak 100 Gm. of French gelatine in chloroform
water, drain when soft, and dissolve with heat in 750 Gm. of glycerine. Add
400 Gm. of chloroform water, with which has been incorporated about 50
Gm. of fresh egg albumen, mix thoroughly, and heat to boiling point for
about 5 minutes. Make up the total weight to 1550 Gm. with chloroform
water and filter in a warm chamber.
Squire (Canada Balsam).—Dry the balsam over a water bath until brittle
when cooled, then to each 200 Gm. add 100 C.c. of benzole or rather less
xylol.
glycerine, and water. Lee recommends the addition of 0·5 to 0·75 per cent.
of acetic acid.
Lee’s Turpentine Colophonium Mounting Medium.—This is highly
recommended for general work, and is prepared by adding small pieces of
colophonium to rectified oil of turpentine, heating in a stove, and when the
solution is sufficiently thick filtering twice in the stove.
Seaman (Glycerine Jelly).—Dissolve isinglass in water so as to make a jelly
that remains stiff at the ordinary temperature of the room, and add one-tenth
part of glycerine, together with a little solution of borax, carbolic acid, or
camphor water. Filter through muslin whilst warm and add a little alcohol.
Seiler (Alcohol Balsam).—Heat Canada balsam until it becomes brittle
when cold, then dissolve in warm absolute alcohol and filter through
absorbent cotton-wool. This is chiefly useful as a mounting medium for
objects stained with carmine.
Squire (Farrant’s Medium).—Dissolve in 200 C.c. of distilled water 1 Gm.
of arsenious acid and 130 Gm. of gum arabic, then add 100 C.c. of
glycerine. Filter through fine Swedish filter paper upon which has been
deposited a thin layer of talc.
Squire (Glycerine and Gum).—Dissolve 130 Gm. of gum arabic in 200 C.c.
of chloroform water (1 in 200), then add 100 C.c. of glycerine and filter.
Squire (Glycerine Jelly).—Soak 100 Gm. of French gelatine in chloroform
water, drain when soft, and dissolve with heat in 750 Gm. of glycerine. Add
400 Gm. of chloroform water, with which has been incorporated about 50
Gm. of fresh egg albumen, mix thoroughly, and heat to boiling point for
about 5 minutes. Make up the total weight to 1550 Gm. with chloroform
water and filter in a warm chamber.
Squire (Canada Balsam).—Dry the balsam over a water bath until brittle
when cooled, then to each 200 Gm. add 100 C.c. of benzole or rather less
xylol.
Page 783
Squire (Dammar Solution).—(1) Dissolve 100 Gm. of dammar in 100 C.c.
of benzole. (2) Dissolve 100 Gm. of dammar in 200 C.c. of turpentine oil,
and add 50 Gm. of mastic dissolved in 200 C.c. of chloroform.
Squire (Potassium Acetate Solution).—Dissolve 250 Gm. of potassium
acetate in 100 C.c. of water, by the aid of gentle heat, and filter. This is used
as a mounting medium.
Squire (Treatment of Sections).—Imbed tissues to be cut in paraffin melting
between 45° and 50° C., according to the temperature of the room and the
nature of the material. Afterwards preserve the sections, prior to staining
and mounting, in 50 per cent. alcohol, or in a mixture of equal volumes of
glycerine and thymol water (1 in 1500). Sections may be conveniently
washed in alcohol, dehydrated, and cleared, in small wide-mouthed bottles.
Topping’s Solution.—-Mix 1 part of absolute alcohol with 5 parts of water,
or 4 parts of water and 1 part of aluminium acetate. Add an equal volume of
glycerine before use.
STAINS AND STAINING METHODS.
Apáthy’s Hæmatoxylin Stain.—After staining in 1 per cent. solution of
hæmatoxylin in 70 or 80 per cent. alcohol, wash out in 1 per cent. solution
of potassium bichromate in alcohol of the same strength. The bichromate
solution should be freshly made by mixing 1 part of a 5 per cent. aqueous
solution with about 4 parts of 80 to 90 per cent. alcohol.
Alferow (Silver Staining).—An acid solution of silver picrate, lactate,
acetate, or citrate, is prepared by adding to 800 C.c. of the solution 10 to 15
drops of a concentrated solution of the acid of the salt taken.
Bethe’s Stain for Chitin.—Place series of mounted sections on slides in a
freshly prepared 10 per cent. solution of aniline hydrochloride, containing 1
drop of hydrochloric acid for each 10 C.c., for 3 or 4 minutes, then rinse in
water, and put the slide with sections downwards in a 10 per cent. solution
of potassium bichromate. The process may be repeated if the stain is not
of benzole. (2) Dissolve 100 Gm. of dammar in 200 C.c. of turpentine oil,
and add 50 Gm. of mastic dissolved in 200 C.c. of chloroform.
Squire (Potassium Acetate Solution).—Dissolve 250 Gm. of potassium
acetate in 100 C.c. of water, by the aid of gentle heat, and filter. This is used
as a mounting medium.
Squire (Treatment of Sections).—Imbed tissues to be cut in paraffin melting
between 45° and 50° C., according to the temperature of the room and the
nature of the material. Afterwards preserve the sections, prior to staining
and mounting, in 50 per cent. alcohol, or in a mixture of equal volumes of
glycerine and thymol water (1 in 1500). Sections may be conveniently
washed in alcohol, dehydrated, and cleared, in small wide-mouthed bottles.
Topping’s Solution.—-Mix 1 part of absolute alcohol with 5 parts of water,
or 4 parts of water and 1 part of aluminium acetate. Add an equal volume of
glycerine before use.
STAINS AND STAINING METHODS.
Apáthy’s Hæmatoxylin Stain.—After staining in 1 per cent. solution of
hæmatoxylin in 70 or 80 per cent. alcohol, wash out in 1 per cent. solution
of potassium bichromate in alcohol of the same strength. The bichromate
solution should be freshly made by mixing 1 part of a 5 per cent. aqueous
solution with about 4 parts of 80 to 90 per cent. alcohol.
Alferow (Silver Staining).—An acid solution of silver picrate, lactate,
acetate, or citrate, is prepared by adding to 800 C.c. of the solution 10 to 15
drops of a concentrated solution of the acid of the salt taken.
Bethe’s Stain for Chitin.—Place series of mounted sections on slides in a
freshly prepared 10 per cent. solution of aniline hydrochloride, containing 1
drop of hydrochloric acid for each 10 C.c., for 3 or 4 minutes, then rinse in
water, and put the slide with sections downwards in a 10 per cent. solution
of potassium bichromate. The process may be repeated if the stain is not
Page 784
sufficiently intense, but the sections must be well rinsed with water after
each immersion.
Beale’s Ammonia Carmine.—Carmine, 10 grs.; strong solution of ammonia,
30 mins.; distilled water, 2 ozs.; alcohol, 0·5 oz.; glycerine, 2 ozs. Dissolve
the carmine in the ammonia by the aid of heat, boil for a few seconds, and
let the solution cool. Then allow the excess of ammonia to evaporate, add
the other ingredients, and filter. If any carmine should deposit on keeping
add one or two drops of ammonia solution to redissolve it.
Benda’s Copper Hæmatoxylin.—Harden the material with chromic acid or
Flemming’s solution and leave sections for 24 hours in a 5 per cent.
solution of neutral copper acetate at a temperature of about 40° C., wash out
well with distilled water, and stain to a dark grey or blackish tint in a
saturated aqueous hæmatoxylin solution. Decolourise the sections in 0·2 per
cent. hydrochloric acid until light yellow, put back into the copper solution
until they turn bluish-grey, then wash, dehydrate, clear, and mount in
balsam.
Bismarck Brown.—Vesuvine 0·5 Gm., rectified spirit 2, and distilled water
80 C.c.; or a concentrated alcoholic solution may be kept ready for dilution.
Bochmer’s Hæmatoxylin.—Dissolve (a) crystallised hæmatoxylin, 1 Gm.,
in absolute alcohol, 10 C.c., and (b) alum ammonia, 10 Gm., in distilled
water, 200 C.c. Mix the two solutions, and allow to ripen for some days
before use. Filter after standing a week. Wash out with aqueous solution of
alum (0·5 per cent.) or with acids.
Calberla’s Indulin Stain.—Dilute a concentrated aqueous solution with 6
volumes of water and stain sections for 5 to 20 minutes. Afterwards wash in
water or alcohol, and examine in glycerine or clove oil.
Calberla’s Macerating Mixture (for nerve and muscle of embryos).—
Dissolve potassium chloride, 0·4 Gm., sodium chloride, 0·3 Gm., sodium
phosphate, 0·2 Gm., and calcium chloride, 0·2 Gm., in water, 100 Gm.,
saturated with carbon dioxide just before using. Mix one volume of this
solution with half a volume of Müller’s solution and one volume of water.
The Müller’s solution may be replaced by a 2·5 per cent. solution of
each immersion.
Beale’s Ammonia Carmine.—Carmine, 10 grs.; strong solution of ammonia,
30 mins.; distilled water, 2 ozs.; alcohol, 0·5 oz.; glycerine, 2 ozs. Dissolve
the carmine in the ammonia by the aid of heat, boil for a few seconds, and
let the solution cool. Then allow the excess of ammonia to evaporate, add
the other ingredients, and filter. If any carmine should deposit on keeping
add one or two drops of ammonia solution to redissolve it.
Benda’s Copper Hæmatoxylin.—Harden the material with chromic acid or
Flemming’s solution and leave sections for 24 hours in a 5 per cent.
solution of neutral copper acetate at a temperature of about 40° C., wash out
well with distilled water, and stain to a dark grey or blackish tint in a
saturated aqueous hæmatoxylin solution. Decolourise the sections in 0·2 per
cent. hydrochloric acid until light yellow, put back into the copper solution
until they turn bluish-grey, then wash, dehydrate, clear, and mount in
balsam.
Bismarck Brown.—Vesuvine 0·5 Gm., rectified spirit 2, and distilled water
80 C.c.; or a concentrated alcoholic solution may be kept ready for dilution.
Bochmer’s Hæmatoxylin.—Dissolve (a) crystallised hæmatoxylin, 1 Gm.,
in absolute alcohol, 10 C.c., and (b) alum ammonia, 10 Gm., in distilled
water, 200 C.c. Mix the two solutions, and allow to ripen for some days
before use. Filter after standing a week. Wash out with aqueous solution of
alum (0·5 per cent.) or with acids.
Calberla’s Indulin Stain.—Dilute a concentrated aqueous solution with 6
volumes of water and stain sections for 5 to 20 minutes. Afterwards wash in
water or alcohol, and examine in glycerine or clove oil.
Calberla’s Macerating Mixture (for nerve and muscle of embryos).—
Dissolve potassium chloride, 0·4 Gm., sodium chloride, 0·3 Gm., sodium
phosphate, 0·2 Gm., and calcium chloride, 0·2 Gm., in water, 100 Gm.,
saturated with carbon dioxide just before using. Mix one volume of this
solution with half a volume of Müller’s solution and one volume of water.
The Müller’s solution may be replaced by a 2·5 per cent. solution of
Page 785
ammonium chromate. Tissues macerated in this mixture are isolated by
teasing and shaking, and mount specimens in concentrated potassium
acetate solution.
Canoy’s Salt Solution.—Add a trace of osmic acid to a 0·75 per cent.
solution of sodium chloride in water.
Chenzinsky’s Methylene Blue and Eosine.—Mix saturated aqueous
solution of methylene blue, 40 parts, with 0·5 per cent. solution of eosine in
70 per cent. alcohol, 20 parts, and distilled water or glycerine, 40 parts.
Cohnheim’s Gold Method.—Place pieces of tissue in 0·5 per cent. gold
chloride solution until quite yellow, then expose to light in water acidulated
with acetic acid until the gold is thoroughly reduced. Mount specimens in
acidulated glycerine.
Crookshank’s Method of Staining Flagella.—Cover-glass preparations
are stained with a drop of concentrated alcoholic solution of gentian violet,
then rinsed in water, allowed to dry, and mounted in balsam.
Czoker’s Alum Cochineal.—Dissolve alum 1 Gm. in distilled water, 100
C.c., add powdered cochineal, 1 Gm., and boil; evaporate down to half of
its original bulk, filter, and add ½ C.c. of liquid carbolic acid.
Delafield’s Hæmatoxylin.—Dissolve hæmatoxylin, 4 Gm., in absolute
alcohol, 25 C.c., and add the solution to 400 C.c. of a saturated aqueous
solution of ammonia alum. Expose the mixture to light and air for 3 or 4
days, then filter and add glycerine, 100 C.c., and methylic alcohol, 100 C.c.
Again expose the solution to light until it becomes dark-coloured, then filter
and preserve in a stoppered bottle.
Ehrlich’s Acid Hæmatoxylin.—Dissolve hæmatoxylin, 2 Gm., in absolute
alcohol, 100 C.c., and add glycerine, 100 C.c., distilled water, 100 C.c.,
ammonia alum, 2 Gm., glacial acetic acid, 10 C.c. Expose to daylight for at
least a month before use, removing the stopper at intervals.
Ehrlich’s Hæmatoxylin (Ammoniated).—Dissolve ammonium carbonate,
0·4 Gm., and hæmatoxylin, 2 Gm., in proof spirit, 40 C.c., and expose to
teasing and shaking, and mount specimens in concentrated potassium
acetate solution.
Canoy’s Salt Solution.—Add a trace of osmic acid to a 0·75 per cent.
solution of sodium chloride in water.
Chenzinsky’s Methylene Blue and Eosine.—Mix saturated aqueous
solution of methylene blue, 40 parts, with 0·5 per cent. solution of eosine in
70 per cent. alcohol, 20 parts, and distilled water or glycerine, 40 parts.
Cohnheim’s Gold Method.—Place pieces of tissue in 0·5 per cent. gold
chloride solution until quite yellow, then expose to light in water acidulated
with acetic acid until the gold is thoroughly reduced. Mount specimens in
acidulated glycerine.
Crookshank’s Method of Staining Flagella.—Cover-glass preparations
are stained with a drop of concentrated alcoholic solution of gentian violet,
then rinsed in water, allowed to dry, and mounted in balsam.
Czoker’s Alum Cochineal.—Dissolve alum 1 Gm. in distilled water, 100
C.c., add powdered cochineal, 1 Gm., and boil; evaporate down to half of
its original bulk, filter, and add ½ C.c. of liquid carbolic acid.
Delafield’s Hæmatoxylin.—Dissolve hæmatoxylin, 4 Gm., in absolute
alcohol, 25 C.c., and add the solution to 400 C.c. of a saturated aqueous
solution of ammonia alum. Expose the mixture to light and air for 3 or 4
days, then filter and add glycerine, 100 C.c., and methylic alcohol, 100 C.c.
Again expose the solution to light until it becomes dark-coloured, then filter
and preserve in a stoppered bottle.
Ehrlich’s Acid Hæmatoxylin.—Dissolve hæmatoxylin, 2 Gm., in absolute
alcohol, 100 C.c., and add glycerine, 100 C.c., distilled water, 100 C.c.,
ammonia alum, 2 Gm., glacial acetic acid, 10 C.c. Expose to daylight for at
least a month before use, removing the stopper at intervals.
Ehrlich’s Hæmatoxylin (Ammoniated).—Dissolve ammonium carbonate,
0·4 Gm., and hæmatoxylin, 2 Gm., in proof spirit, 40 C.c., and expose to
Page 786
the air in a shallow dish for 24 hours. Then make up the volume to 40 C.c.
with proof spirit (warming if necessary to re-dissolve any separate crystals),
and add ammonia alum, 2 Gm., dissolved in distilled water, 80 C.c.,
together with glycerine, 100 C.c., rectified spirit, 80 C.c., and glacial acetic
acid, 10 C.c.
Ehrlich-Biondi Mixture (or Ehrlich-Biondi-Heidenheim mixture).—
Dissolve (a) methyl green, 0·5 Gm., in distilled water, 100 C.c.; (b) acid
fuchsine, 0·5 Gm., in distilled water, 40 C.c.; (c) orange, 2 Gm., in distilled
water, 200 C.c. Mix the three solutions and filter before use. Stain sections
for 12 hours, then wash, dehydrate, clear, and mount.
Ehrlich-Weigert-Koch’s Gentian-Violet-Aniline-Water.—Aniline water,
100 C.c., concentrated alcoholic solution of gentian violet, 11 C.c.; absolute
alcohol, 10 C.c.
Everard, Demoor, and Massart’s Hæmatoxylin-Eosine.—Dissolve alum,
20 Gm., in water, 200 Gm., by the aid of heat, then filter, and after 24 hours
add a solution of hæmatoxylin, 1 Gm., in alcohol, 10 Gm. Let the solution
stand for 8 days, again filter, and mix with an equal volume of the following
solution:—Eosine, 1 Gm., alcohol, 25 Gm., water, 75 Gm., glycerine, 50
Gm.
Flemming’s Gentian Violet Method.—Use a concentrated alcoholic
solution of Gentian Violet diluted with about one half its bulk of water.
Differentiate the stained objects in alcohol acidulated with about 0·5 per
cent. of hydrochloric acid, followed by pure alcohol and clove oil.
Flemming’s Orange Method.—Stain for days or weeks in strong alcoholic
safranine solution diluted with half its bulk of aniline water (saturated); then
rinse in distilled water, differentiate in absolute alcohol containing 0·1 per
cent. of hydrochloric acid, stain for 1 to 3 hours in strong aqueous gentian
violet solution, again wash in distilled water, and finally treat with
concentrated aqueous solution of Orange. After a few minutes transfer
sections to absolute alcohol, then clear in clove or bergamot oil, and mount
in dammar or balsam.
with proof spirit (warming if necessary to re-dissolve any separate crystals),
and add ammonia alum, 2 Gm., dissolved in distilled water, 80 C.c.,
together with glycerine, 100 C.c., rectified spirit, 80 C.c., and glacial acetic
acid, 10 C.c.
Ehrlich-Biondi Mixture (or Ehrlich-Biondi-Heidenheim mixture).—
Dissolve (a) methyl green, 0·5 Gm., in distilled water, 100 C.c.; (b) acid
fuchsine, 0·5 Gm., in distilled water, 40 C.c.; (c) orange, 2 Gm., in distilled
water, 200 C.c. Mix the three solutions and filter before use. Stain sections
for 12 hours, then wash, dehydrate, clear, and mount.
Ehrlich-Weigert-Koch’s Gentian-Violet-Aniline-Water.—Aniline water,
100 C.c., concentrated alcoholic solution of gentian violet, 11 C.c.; absolute
alcohol, 10 C.c.
Everard, Demoor, and Massart’s Hæmatoxylin-Eosine.—Dissolve alum,
20 Gm., in water, 200 Gm., by the aid of heat, then filter, and after 24 hours
add a solution of hæmatoxylin, 1 Gm., in alcohol, 10 Gm. Let the solution
stand for 8 days, again filter, and mix with an equal volume of the following
solution:—Eosine, 1 Gm., alcohol, 25 Gm., water, 75 Gm., glycerine, 50
Gm.
Flemming’s Gentian Violet Method.—Use a concentrated alcoholic
solution of Gentian Violet diluted with about one half its bulk of water.
Differentiate the stained objects in alcohol acidulated with about 0·5 per
cent. of hydrochloric acid, followed by pure alcohol and clove oil.
Flemming’s Orange Method.—Stain for days or weeks in strong alcoholic
safranine solution diluted with half its bulk of aniline water (saturated); then
rinse in distilled water, differentiate in absolute alcohol containing 0·1 per
cent. of hydrochloric acid, stain for 1 to 3 hours in strong aqueous gentian
violet solution, again wash in distilled water, and finally treat with
concentrated aqueous solution of Orange. After a few minutes transfer
sections to absolute alcohol, then clear in clove or bergamot oil, and mount
in dammar or balsam.
Page 787
Fol’s Ferric Chloride Fixing and Staining Process.—Preparations are
treated with tincture of ferric chloride diluted with 5 to 10 times its bulk of
70 per cent. alcohol, and then transfer for 24 hours to alcohol containing a
trace of gallic acid.
Frey’s Fuchsine Solution.—A solution of 0·01 Gm. of crystallised
fuchsine, 20 to 25 drops absolute alcohol, and 15 C.c. of water.
Friedlaender’s Staining Methods.—Cover-glass preparations are treated
for 3 minutes with a 1 per cent. solution of acetic acid, and allowed to dry
after removal of excess of liquid by filter paper. Next place them in gentian
violet aniline water (aniline water, 100 C.c., concentrated alcoholic solution
of gentian violet, 11 C.c.; absolute alcohol, 10 C.c.) for half a minute, wash
in water, mount and dry in balsam. Sections are kept for 24 hours in a warm
place, in the following solution:—Concentrated alcoholic solution of
gentian violet, 50 C.c.; distilled water, 100 C.c.; glacial acetic acid, 10 C.c.
Then treat for 1 or 2 minutes with 0·1 per cent. acetic acid, dehydrate, clear,
and mount in balsam.
Gaffky’s Staining Methods.—Sections of material hardened in alcohol are
left for 20 to 24 hours in a deep blue opaque solution, freshly made by
adding saturated alcoholic solution of methylene blue to distilled water.
Then wash in distilled water, dehydrate in absolute alcohol, clear in
turpentine oil, and mount in balsam.
Giacomi’s Staining Method.—Stain cover-glass preparations for a few
minutes in a hot solution of fuchsine, then place in water containing a few
drops of ferric chloride solution, and afterwards decolourise in strong ferric
chloride solution. If any precipitate be formed with the iron solution,
complete the decolourisation in alcohol. Counterstain with vesuvine.
Gibbes’ Double Staining Method.—Well mix magenta, 2 Gm., and
methylene blue, 1 Gm., then add slowly aniline oil, 3 C.c., dissolve in
rectified spirit, 15 C.c. Subsequently add 15 C.c. of distilled water and keep
the stain in a stoppered bottle. Cover-glass preparations are placed for 4
minutes in the slightly heated stain and sections left for some hours in the
stain at the ordinary temperature. Afterwards, wash in methylated spirit
treated with tincture of ferric chloride diluted with 5 to 10 times its bulk of
70 per cent. alcohol, and then transfer for 24 hours to alcohol containing a
trace of gallic acid.
Frey’s Fuchsine Solution.—A solution of 0·01 Gm. of crystallised
fuchsine, 20 to 25 drops absolute alcohol, and 15 C.c. of water.
Friedlaender’s Staining Methods.—Cover-glass preparations are treated
for 3 minutes with a 1 per cent. solution of acetic acid, and allowed to dry
after removal of excess of liquid by filter paper. Next place them in gentian
violet aniline water (aniline water, 100 C.c., concentrated alcoholic solution
of gentian violet, 11 C.c.; absolute alcohol, 10 C.c.) for half a minute, wash
in water, mount and dry in balsam. Sections are kept for 24 hours in a warm
place, in the following solution:—Concentrated alcoholic solution of
gentian violet, 50 C.c.; distilled water, 100 C.c.; glacial acetic acid, 10 C.c.
Then treat for 1 or 2 minutes with 0·1 per cent. acetic acid, dehydrate, clear,
and mount in balsam.
Gaffky’s Staining Methods.—Sections of material hardened in alcohol are
left for 20 to 24 hours in a deep blue opaque solution, freshly made by
adding saturated alcoholic solution of methylene blue to distilled water.
Then wash in distilled water, dehydrate in absolute alcohol, clear in
turpentine oil, and mount in balsam.
Giacomi’s Staining Method.—Stain cover-glass preparations for a few
minutes in a hot solution of fuchsine, then place in water containing a few
drops of ferric chloride solution, and afterwards decolourise in strong ferric
chloride solution. If any precipitate be formed with the iron solution,
complete the decolourisation in alcohol. Counterstain with vesuvine.
Gibbes’ Double Staining Method.—Well mix magenta, 2 Gm., and
methylene blue, 1 Gm., then add slowly aniline oil, 3 C.c., dissolve in
rectified spirit, 15 C.c. Subsequently add 15 C.c. of distilled water and keep
the stain in a stoppered bottle. Cover-glass preparations are placed for 4
minutes in the slightly heated stain and sections left for some hours in the
stain at the ordinary temperature. Afterwards, wash in methylated spirit
Page 788
until no more colour comes away, then dehydrate, clear in cedar oil, and
mount in balsam.
Gibbes’ Magenta Stain.—Mix magenta, 2 Gm.; aniline oil, 3 Gm.; rectified
spirit, 20 C.c.; and distilled water, 20 C.c.
Golgi’s Sublimated Method.—Small cubes of tissue are hardened for 15 to
30 days in Müller’s fluid, which should be frequently changed. Then
transfer for 8 to 10 days to 0·25 to 1 per cent. aqueous mercuric chloride
solution, which must be changed, as it becomes coloured. If desired, treat
subsequently with weak sodium sulphide solution to darken the stain and
make it sharper. After cutting sections from material thus prepared they
must be well washed with water.
Gram’s Stain for Bacteria.—This is prepared by shaking 15 drops of
aniline oil with 15 Gm. of water, filtering the solution and adding to the
filtrate 4 to 5 drops of saturated alcoholic solution of gentian violet. Or
shake 3·3 C.c. of aniline with 100 C.c. of distilled water and, after filtering,
add 11 C.c. of concentrated alcoholic solution of gentian violet and 10 C.c.
of absolute alcohol. After preparations have been stained for 1 to 3 minutes
in one of the above they are quickly rinsed in absolute alcohol and then
placed in Gram’s solution of iodine in potassium iodine (iodine, 1 Gm.;
potassium iodine, 2 Gm.; water, 300 C.c.), until they have acquired a brown
colour. This takes about 1 to 3 minutes, and they are next washed in 90 per
cent. alcohol until they become pale yellow, then dehydrated, cleared, and
mounted in balsam. Counterstain with eosine or vesuvine if desired.
Gram’s Solution.—Iodine, 1 Gm.; potassium iodine, 2 Gm.; distilled water,
300 Gm.
Grenacher’s Alum Carmine.—Dissolve 5 Gm. of ammonium alum in 100
C.c. of distilled water, add 1 Gm. of carmine, and boil for 20 minutes, filter
when cool, and add distilled water to make up to 100 C.c.
Grenacher’s Alcoholic Borax Carmine.—Dissolve 4 Gm. of borax in 100
C.c. of distilled water, then add 3 Gm. of carmine, and heat gently. Finally,
add 100 C.c. of 70 per cent. alcohol, filter the solution, if necessary, before
mount in balsam.
Gibbes’ Magenta Stain.—Mix magenta, 2 Gm.; aniline oil, 3 Gm.; rectified
spirit, 20 C.c.; and distilled water, 20 C.c.
Golgi’s Sublimated Method.—Small cubes of tissue are hardened for 15 to
30 days in Müller’s fluid, which should be frequently changed. Then
transfer for 8 to 10 days to 0·25 to 1 per cent. aqueous mercuric chloride
solution, which must be changed, as it becomes coloured. If desired, treat
subsequently with weak sodium sulphide solution to darken the stain and
make it sharper. After cutting sections from material thus prepared they
must be well washed with water.
Gram’s Stain for Bacteria.—This is prepared by shaking 15 drops of
aniline oil with 15 Gm. of water, filtering the solution and adding to the
filtrate 4 to 5 drops of saturated alcoholic solution of gentian violet. Or
shake 3·3 C.c. of aniline with 100 C.c. of distilled water and, after filtering,
add 11 C.c. of concentrated alcoholic solution of gentian violet and 10 C.c.
of absolute alcohol. After preparations have been stained for 1 to 3 minutes
in one of the above they are quickly rinsed in absolute alcohol and then
placed in Gram’s solution of iodine in potassium iodine (iodine, 1 Gm.;
potassium iodine, 2 Gm.; water, 300 C.c.), until they have acquired a brown
colour. This takes about 1 to 3 minutes, and they are next washed in 90 per
cent. alcohol until they become pale yellow, then dehydrated, cleared, and
mounted in balsam. Counterstain with eosine or vesuvine if desired.
Gram’s Solution.—Iodine, 1 Gm.; potassium iodine, 2 Gm.; distilled water,
300 Gm.
Grenacher’s Alum Carmine.—Dissolve 5 Gm. of ammonium alum in 100
C.c. of distilled water, add 1 Gm. of carmine, and boil for 20 minutes, filter
when cool, and add distilled water to make up to 100 C.c.
Grenacher’s Alcoholic Borax Carmine.—Dissolve 4 Gm. of borax in 100
C.c. of distilled water, then add 3 Gm. of carmine, and heat gently. Finally,
add 100 C.c. of 70 per cent. alcohol, filter the solution, if necessary, before
Page 789
use. Pieces of tissues are stained in this for 1 to 3 days, and then transferred
to 70 per cent. alcohol, containing 0·5 to 1 per cent. of hydrochloric acid.
Heidenhain’s Hæmatoxylin Method.—Dissolve (a) hæmatoxylin, 1 Gm., in
distilled water, 300 C.c.; (b) potassium chromate, 1 Gm., in distilled water,
200 C.c. Small pieces of tissue hardened in alcohol or picric acid are placed
in (a) for 12 to 24 hours, and then transferred for a similar length of time to
(b). Wash thoroughly in water, dehydrate in alcohol, and imbed in paraffin.
Henle’s Stain (for nervous tissue).—Sections are left in palladium chloride
solution (1:300 to 1:600) till they are of a straw colour, then rinsed in water
and stained with strong ammonia carmine.
Henneguy’s Alum Carmine.—Excess of carmine is boiled in saturated
solution of potash alum, and 10 per cent. of glacial acetic acid added on
cooling. Allow to settle for some days, and then filter.
Henneguy’s Permanganate Method.—Treat sections for 5 minutes with 1
per cent. potassium permanganate solution, then wash in water and stain
with safranine, rubin, gentian violet, vesuvine, preference being given to a
safranine solution prepared with aniline water.
Hermann’s Platino-aceto-osmic Mixture.—Mix 15 parts of 1 per cent.
platinic chloride solution, 1 part of glacial acetic acid, and 2 or 4 parts of 2
per cent. osmic acid.
Hertwig’s Macerating Fluid.—Mix equal parts of 0·05 per cent. osmic
acid, and 0·2 per cent. acetic acid. Medusæ are treated with this mixture for
2 or 3 minutes, then washed in 0·1 per cent. acetic acid until free from
osmic acid. Leave them for 24 hours in the dilute acetic acid, then wash in
water, stain with Beale’s carmine, and mount in glycerine. For Actiniæ use
0·04 per cent. osmic acid and make both solutions with sea water. Wash out
with 0·2 per cent. acetic acid, and stain with picro-carmine.
Hessert’s Method for Staining Flagella.—Fix the film by treating cover-
glass preparations with a saturated alcoholic solution of mercuric chloride,
wash, and stain for 30 or 40 minutes in a hot 10 per cent. aqueous solution
of saturated alcoholic solution of fuchsine.
to 70 per cent. alcohol, containing 0·5 to 1 per cent. of hydrochloric acid.
Heidenhain’s Hæmatoxylin Method.—Dissolve (a) hæmatoxylin, 1 Gm., in
distilled water, 300 C.c.; (b) potassium chromate, 1 Gm., in distilled water,
200 C.c. Small pieces of tissue hardened in alcohol or picric acid are placed
in (a) for 12 to 24 hours, and then transferred for a similar length of time to
(b). Wash thoroughly in water, dehydrate in alcohol, and imbed in paraffin.
Henle’s Stain (for nervous tissue).—Sections are left in palladium chloride
solution (1:300 to 1:600) till they are of a straw colour, then rinsed in water
and stained with strong ammonia carmine.
Henneguy’s Alum Carmine.—Excess of carmine is boiled in saturated
solution of potash alum, and 10 per cent. of glacial acetic acid added on
cooling. Allow to settle for some days, and then filter.
Henneguy’s Permanganate Method.—Treat sections for 5 minutes with 1
per cent. potassium permanganate solution, then wash in water and stain
with safranine, rubin, gentian violet, vesuvine, preference being given to a
safranine solution prepared with aniline water.
Hermann’s Platino-aceto-osmic Mixture.—Mix 15 parts of 1 per cent.
platinic chloride solution, 1 part of glacial acetic acid, and 2 or 4 parts of 2
per cent. osmic acid.
Hertwig’s Macerating Fluid.—Mix equal parts of 0·05 per cent. osmic
acid, and 0·2 per cent. acetic acid. Medusæ are treated with this mixture for
2 or 3 minutes, then washed in 0·1 per cent. acetic acid until free from
osmic acid. Leave them for 24 hours in the dilute acetic acid, then wash in
water, stain with Beale’s carmine, and mount in glycerine. For Actiniæ use
0·04 per cent. osmic acid and make both solutions with sea water. Wash out
with 0·2 per cent. acetic acid, and stain with picro-carmine.
Hessert’s Method for Staining Flagella.—Fix the film by treating cover-
glass preparations with a saturated alcoholic solution of mercuric chloride,
wash, and stain for 30 or 40 minutes in a hot 10 per cent. aqueous solution
of saturated alcoholic solution of fuchsine.
Page 790
Hoffmann’s Blue Stain.—Dissolve 1 Gm. of Hoffmann’s blue in 20 C.c. of
rectified spirit and 80 C.c. of distilled water, then add 0·5 C.c. of glacial
acetic acid. As a nuclear stain immerse sections for 10 minutes or more,
rinse in water, wash in 90 per cent. alcohol, dehydrate, clear, and mount in
balsam. To stain sieve areas, less time is required, 5 to 10 minutes, rinse in
distilled water, and mount in glycerine; or dehydrate, clear, and mount in
balsam.
Hoyer’s Shellac Injection Mass.—Dissolve shellac in 80 per cent. alcohol
to the consistency of a thin syrup, and strain through muslin of medium
thickness. Colour with aniline colours in alcoholic solution, or by means of
vermilion or other pigment suspended in alcohol.
Hoyer’s Silver Nitrate Gelatine Mass.—Mix a concentrated solution of
gelatine with an equal volume of a 4 per cent. silver nitrate solution and
warm, then add a very small quantity of aqueous pyrogallic acid solution to
reduce the silver salt, and add chloral and glycerine as in the carmine
gelatine mass.
Hoyer’s Silver Stain.—Add ammonia to a solution of silver nitrate of
known strength, until the precipitate formed just re-dissolves, then dilute
the solution until it contains 0·75 to 0·50 per cent. of the salt.
Kaiser’s Bismarck Brown Stain. Sections are stained for 48 hours, at a
temperature of 60 C., in a saturated solution of Bismarck brown in 60 per
cent. alcohol, and washed out in 60 per cent. alcohol containing 2 per cent.
of H.C.L., or 3 per cent. of acetic acid.
Kaiser’s Nerve Stain.—This is a modification of Weigert’s process. The
material is hardened in Müller’s solution for 2 or 3 days, then cut into slices
2 to 4 Mm. thick, and treated with the solution for 5 or 6 days more.
Subsequently immerse in Marchi’s solution for 8 days, then wash, pass
through alcohol, and imbed in celloidin. Sections are mordanted for 5
minutes in the following mixture:—Solutions of ferric chloride, 1 part;
distilled water, 1 part; rectified spirit, 8 parts. Next wash in Weigert’s
hæmatoxylin, and warm in a fresh quantity of the same for a few minutes,
wash with water, differentiate in Pal’s solution, and neutralise the oxalic
acid by washing in water containing a little ammonia.
rectified spirit and 80 C.c. of distilled water, then add 0·5 C.c. of glacial
acetic acid. As a nuclear stain immerse sections for 10 minutes or more,
rinse in water, wash in 90 per cent. alcohol, dehydrate, clear, and mount in
balsam. To stain sieve areas, less time is required, 5 to 10 minutes, rinse in
distilled water, and mount in glycerine; or dehydrate, clear, and mount in
balsam.
Hoyer’s Shellac Injection Mass.—Dissolve shellac in 80 per cent. alcohol
to the consistency of a thin syrup, and strain through muslin of medium
thickness. Colour with aniline colours in alcoholic solution, or by means of
vermilion or other pigment suspended in alcohol.
Hoyer’s Silver Nitrate Gelatine Mass.—Mix a concentrated solution of
gelatine with an equal volume of a 4 per cent. silver nitrate solution and
warm, then add a very small quantity of aqueous pyrogallic acid solution to
reduce the silver salt, and add chloral and glycerine as in the carmine
gelatine mass.
Hoyer’s Silver Stain.—Add ammonia to a solution of silver nitrate of
known strength, until the precipitate formed just re-dissolves, then dilute
the solution until it contains 0·75 to 0·50 per cent. of the salt.
Kaiser’s Bismarck Brown Stain. Sections are stained for 48 hours, at a
temperature of 60 C., in a saturated solution of Bismarck brown in 60 per
cent. alcohol, and washed out in 60 per cent. alcohol containing 2 per cent.
of H.C.L., or 3 per cent. of acetic acid.
Kaiser’s Nerve Stain.—This is a modification of Weigert’s process. The
material is hardened in Müller’s solution for 2 or 3 days, then cut into slices
2 to 4 Mm. thick, and treated with the solution for 5 or 6 days more.
Subsequently immerse in Marchi’s solution for 8 days, then wash, pass
through alcohol, and imbed in celloidin. Sections are mordanted for 5
minutes in the following mixture:—Solutions of ferric chloride, 1 part;
distilled water, 1 part; rectified spirit, 8 parts. Next wash in Weigert’s
hæmatoxylin, and warm in a fresh quantity of the same for a few minutes,
wash with water, differentiate in Pal’s solution, and neutralise the oxalic
acid by washing in water containing a little ammonia.
Page 791
Kaiser’s Stain for the Spinal Cord.—Sections are stained for a few hours
in solution of náphthylamine brown, 1 part, in water, 200 parts, and alcohol,
100 parts. Afterwards wash with alcohol and clear with origanum oil.
Kallin’s Neurological Method.—Dissolve hydroquinone, 5 Gm., sodium
sulphite, 40 Gm., and potassium carbonate, 75 Gm., in 25 Gm. of distilled
water. At the time of using, dilute this solution with one-third to one-half its
bulk of absolute alcohol; immerse sections of silvered material for several
minutes until reduction is complete. Then place them in 70 per cent. alcohol
for 10 to 15 minutes, and subsequently leave in aqueous solution of sodium
hyposulphite (1:5) for 24 hours or more. Finally dehydrate and mount.
Carmine may be used as an afterstain.
Kleinenberg’s Solution (Improved Formula).—Hæmatoxylin, 2½ Gm.;
crystallised calcium chloride, 20 Gm. in 10 C.c. of distilled water; alum, 3
Gm. in 16 C.c. of distilled water; rectified spirit, 240 C.c. Dissolve the
calcium chloride and alum in their respective quantities of water by the aid
of heat; mix the solutions and immediately dilute with rectified spirit; after
an hour filter and add the hæmatoxylin. This makes a good working
solution which keeps well. Of course it contains the alumina in solution, not
as alum but aluminium chloride. If in special cases the colour is considered
too strong, the dilution (when staining in bulk) must be made with some of
the solution to which hæmatoxylin has not been added.
Koch’s Method for Staining Flagella.—Immerse cover-glass preparations
in a 1 per cent. aqueous solution of hæmatoxylin, then transfer to a 5 per
cent. solution of chromic acid or to Müller’s fluid; dry and mount in
balsam.
Koch-Ehrlich, Bacilli.—Place sections, or cover-glass preparations, for at
least 12 hours in gentian violet, or fuchsine aniline water (aniline water, 100
C.c.; concentrated alcoholic solution of gentian violet, or fuchsine, 11 C.c.;
absolute alcohol, 10 C.c.), then immerse in a mixture of pure nitric acid (sp.
gr. 1·42), 10 C.c., and distilled water, 30 C.c., for some seconds. Rinse in 60
per cent. alcohol for a few minutes, and then counterstain with vesuvine
(vesuvine, 0·5 Gm.; rectified spirit, 20 C.c.; distilled water, 80 C.c.) after
gentian violet; or methylene blue (methylene blue, 0·25 Gm.; rectified
spirit, 20 C.c.; distilled water, 80 C.c.) after fuchsine. Finally rinse in water,
in solution of náphthylamine brown, 1 part, in water, 200 parts, and alcohol,
100 parts. Afterwards wash with alcohol and clear with origanum oil.
Kallin’s Neurological Method.—Dissolve hydroquinone, 5 Gm., sodium
sulphite, 40 Gm., and potassium carbonate, 75 Gm., in 25 Gm. of distilled
water. At the time of using, dilute this solution with one-third to one-half its
bulk of absolute alcohol; immerse sections of silvered material for several
minutes until reduction is complete. Then place them in 70 per cent. alcohol
for 10 to 15 minutes, and subsequently leave in aqueous solution of sodium
hyposulphite (1:5) for 24 hours or more. Finally dehydrate and mount.
Carmine may be used as an afterstain.
Kleinenberg’s Solution (Improved Formula).—Hæmatoxylin, 2½ Gm.;
crystallised calcium chloride, 20 Gm. in 10 C.c. of distilled water; alum, 3
Gm. in 16 C.c. of distilled water; rectified spirit, 240 C.c. Dissolve the
calcium chloride and alum in their respective quantities of water by the aid
of heat; mix the solutions and immediately dilute with rectified spirit; after
an hour filter and add the hæmatoxylin. This makes a good working
solution which keeps well. Of course it contains the alumina in solution, not
as alum but aluminium chloride. If in special cases the colour is considered
too strong, the dilution (when staining in bulk) must be made with some of
the solution to which hæmatoxylin has not been added.
Koch’s Method for Staining Flagella.—Immerse cover-glass preparations
in a 1 per cent. aqueous solution of hæmatoxylin, then transfer to a 5 per
cent. solution of chromic acid or to Müller’s fluid; dry and mount in
balsam.
Koch-Ehrlich, Bacilli.—Place sections, or cover-glass preparations, for at
least 12 hours in gentian violet, or fuchsine aniline water (aniline water, 100
C.c.; concentrated alcoholic solution of gentian violet, or fuchsine, 11 C.c.;
absolute alcohol, 10 C.c.), then immerse in a mixture of pure nitric acid (sp.
gr. 1·42), 10 C.c., and distilled water, 30 C.c., for some seconds. Rinse in 60
per cent. alcohol for a few minutes, and then counterstain with vesuvine
(vesuvine, 0·5 Gm.; rectified spirit, 20 C.c.; distilled water, 80 C.c.) after
gentian violet; or methylene blue (methylene blue, 0·25 Gm.; rectified
spirit, 20 C.c.; distilled water, 80 C.c.) after fuchsine. Finally rinse in water,
Page 792
dehydrate, clear, and mount in balsam. According to Squire, who points out
that nitric acid is apt to injure delicate sections, Watson Cheyne
recommends that sections should be transferred from fuchsine aniline water
to distilled water, then rinsed in alcohol, and placed in the following
contrast stain for 1 or 2 hours:—Saturated alcoholic solution of methylene
blue, 20 C.c.; distilled water, 100 C.c.; formic acid (sp. gr. 1·2), 1 C.c.
Kühne’s Carbolic Methylene Blue.—Rub up 1·5 Gm. of methylene blue
with 10 C.c. of absolute alcohol, and add 100 C.c. of a 5 per cent. aqueous
solution of carbolic acid.
Kühne’s Methyl Violet Solution.—Dissolve 1 Gm. of methyl violet in 90
C.c. of distilled water and 100 C.c. of alcohol.
Kühne’s Aniline Oil Solutions.—Rub up as much methylene blue, methyl
green, or safranine as will go upon the point of a knife, with 10 C.c. of
aniline, and allow to settle.
Kühne’s Carbolic Fuchsine or Black Brown.—Dissolve 1 Gm. of
fuchsine or black brown in 10 C.c. of absolute alcohol, and add 100 C.c. of
a 5 per cent. aqueous solution of carbolic acid.
Kühne’s Modification of Gram’s Method.—Stain nuclei with carmine,
then treat sections for 5 minutes in methyl violet solution, diluted one-sixth
with a 1 per cent. aqueous solution of ammonium carbonate, or in a solution
of Victoria blue, 0·25 Gm., in rectified spirit, 20 C.c., and distilled water, 80
C.c. Next rinse thoroughly in water and transfer to Grain’s solution for 2 to
3 minutes; again rinse in water and extract excess of stain with solution of
yellow fluorescine, 1 Gm., in absolute alcohol, 50 C.c. Finally, pass through
pure alcohol, aniline, terebene, and xylol, and mount in balsam.
Löffler’s Solution.—Concentrated alcoholic solution of methylene blue,
30 C.c.; solution of (caustic potash) potassium hydrate (1:10,000), 100 C.c.
Mix and filter shortly before use. Sections are stained for a few minutes
(tubercle sections for some hours), and excess of stain can be removed by
immersion for a few seconds in 0·5 per cent. acetic acid. Dehydrate in
absolute alcohol, clear in cedar oil, and mount in balsam. Löffler found that
that nitric acid is apt to injure delicate sections, Watson Cheyne
recommends that sections should be transferred from fuchsine aniline water
to distilled water, then rinsed in alcohol, and placed in the following
contrast stain for 1 or 2 hours:—Saturated alcoholic solution of methylene
blue, 20 C.c.; distilled water, 100 C.c.; formic acid (sp. gr. 1·2), 1 C.c.
Kühne’s Carbolic Methylene Blue.—Rub up 1·5 Gm. of methylene blue
with 10 C.c. of absolute alcohol, and add 100 C.c. of a 5 per cent. aqueous
solution of carbolic acid.
Kühne’s Methyl Violet Solution.—Dissolve 1 Gm. of methyl violet in 90
C.c. of distilled water and 100 C.c. of alcohol.
Kühne’s Aniline Oil Solutions.—Rub up as much methylene blue, methyl
green, or safranine as will go upon the point of a knife, with 10 C.c. of
aniline, and allow to settle.
Kühne’s Carbolic Fuchsine or Black Brown.—Dissolve 1 Gm. of
fuchsine or black brown in 10 C.c. of absolute alcohol, and add 100 C.c. of
a 5 per cent. aqueous solution of carbolic acid.
Kühne’s Modification of Gram’s Method.—Stain nuclei with carmine,
then treat sections for 5 minutes in methyl violet solution, diluted one-sixth
with a 1 per cent. aqueous solution of ammonium carbonate, or in a solution
of Victoria blue, 0·25 Gm., in rectified spirit, 20 C.c., and distilled water, 80
C.c. Next rinse thoroughly in water and transfer to Grain’s solution for 2 to
3 minutes; again rinse in water and extract excess of stain with solution of
yellow fluorescine, 1 Gm., in absolute alcohol, 50 C.c. Finally, pass through
pure alcohol, aniline, terebene, and xylol, and mount in balsam.
Löffler’s Solution.—Concentrated alcoholic solution of methylene blue,
30 C.c.; solution of (caustic potash) potassium hydrate (1:10,000), 100 C.c.
Mix and filter shortly before use. Sections are stained for a few minutes
(tubercle sections for some hours), and excess of stain can be removed by
immersion for a few seconds in 0·5 per cent. acetic acid. Dehydrate in
absolute alcohol, clear in cedar oil, and mount in balsam. Löffler found that
Page 793
most bacteria stained better in this solution than in the weaker solutions
used by Koch for turbercle bacillus.
Lavdowsky’s Bilberry Juice Stain.—Well wash the fresh berries of
Vaccinium myrtillus, then express the juice and mix with twice its bulk of
distilled water, mixed with a little 90 per cent. alcohol. Heat for a short time
and filter whilst warm. Dilute the stain with 2 or 3 volumes of distilled
water before use.
Lee’s Formaldehyde Solutions.—(1) Mix 1 part of 40 per cent.
formaldehyde solution with two parts of 1 per cent. chromic acid solution,
and add 4 per cent. of acetic acid. (2) Mix 1 part of 40 per cent.
formaldehyde solution with 4 parts of 1 per cent. platinic chloride solution,
and add 2 per cent. of acetic acid.
Lee’s Osmic Acid and Pyrogallol Stain.—Fix the tissues in Hermann’s
mixture or Flemming’s mixture for half an hour, then place in a weak
solution of pyrogallol, which may be prepared with alcohol in some cases.
Safranine may be used as a second stain.
Martinotti’s Picro-nigrosine Stain.—Pathological objects are stained for 2
or 3 hours or days, in a saturated solution of nigrosine in saturated alcoholic
picric acid solution. Then wash out in a mixture of 1 part of formic acid
with 2 parts of alcohol until the grey matter appears clearly differentiated
from the white to the naked eye.
Mayer’s Aluminium Chloride Carmine.—Dissolve 1 Gm. of carminic acid
and 3 Gm. of aluminium chloride in 200 C.c. of water.
Mayer’s Berlin Blue Injection.—Add a solution of 10 C.c. of tincture of
ferric chloride in 500 C.c. of water, to a solution of 20 Gm. of potassium
ferrocyanide in 500 C.c. of water, allow to stand for 12 hours, decant, wash
the deposit for 1 or 2 days with distilled water until the washings come
through dark blue, then dissolve the blue in about a litre of water.
Mayer’s Carmalum.—Dissolve 1 Gm. of carminic acid and 10 Gm. of
alum in 200 C.c. of distilled water; decant, or filter, and add a few crystals
of thymol, 0·1 per cent. of salicylic acid, or 0·5 per cent. of sodium
used by Koch for turbercle bacillus.
Lavdowsky’s Bilberry Juice Stain.—Well wash the fresh berries of
Vaccinium myrtillus, then express the juice and mix with twice its bulk of
distilled water, mixed with a little 90 per cent. alcohol. Heat for a short time
and filter whilst warm. Dilute the stain with 2 or 3 volumes of distilled
water before use.
Lee’s Formaldehyde Solutions.—(1) Mix 1 part of 40 per cent.
formaldehyde solution with two parts of 1 per cent. chromic acid solution,
and add 4 per cent. of acetic acid. (2) Mix 1 part of 40 per cent.
formaldehyde solution with 4 parts of 1 per cent. platinic chloride solution,
and add 2 per cent. of acetic acid.
Lee’s Osmic Acid and Pyrogallol Stain.—Fix the tissues in Hermann’s
mixture or Flemming’s mixture for half an hour, then place in a weak
solution of pyrogallol, which may be prepared with alcohol in some cases.
Safranine may be used as a second stain.
Martinotti’s Picro-nigrosine Stain.—Pathological objects are stained for 2
or 3 hours or days, in a saturated solution of nigrosine in saturated alcoholic
picric acid solution. Then wash out in a mixture of 1 part of formic acid
with 2 parts of alcohol until the grey matter appears clearly differentiated
from the white to the naked eye.
Mayer’s Aluminium Chloride Carmine.—Dissolve 1 Gm. of carminic acid
and 3 Gm. of aluminium chloride in 200 C.c. of water.
Mayer’s Berlin Blue Injection.—Add a solution of 10 C.c. of tincture of
ferric chloride in 500 C.c. of water, to a solution of 20 Gm. of potassium
ferrocyanide in 500 C.c. of water, allow to stand for 12 hours, decant, wash
the deposit for 1 or 2 days with distilled water until the washings come
through dark blue, then dissolve the blue in about a litre of water.
Mayer’s Carmalum.—Dissolve 1 Gm. of carminic acid and 10 Gm. of
alum in 200 C.c. of distilled water; decant, or filter, and add a few crystals
of thymol, 0·1 per cent. of salicylic acid, or 0·5 per cent. of sodium
Page 794
salicylate. A weaker solution contains 3 to 5 times as much alum and 5
times as much water.
Merbel’s Carmine and Indigo Fluids (give a blue and red stain, and are
very selective).—To prepare the red fluid, take—Carmine, 2 dr.; borax, 2
dr.; distilled water, 4 ozs. For the blue fluid, take—Indigo carmine, 2 dr.;
borax, 2 dr.; distilled water, 4 ozs. Mix each in a mortar, and allow it to
stand, then pour off the supernatant fluid. If the sections have been
hardened in chromic acid, picric acid, or a bichromate, they must be washed
in water till no tinge appears. Place them in alcohol for fifteen or twenty
minutes, then in the two fluids mixed in equal proportions, after which
wash them in a saturated aqueous solution of oxalic acid, where they should
remain a rather shorter time than in the staining fluids. When sufficiently
bleached, wash them in water, to get rid of the acid, then pass them through
spirit and oil of cloves, and mount in balsam or dammar.
Mitrophanow’s Gold Process for Prickle-Cells and Intercellular
Canals.—Wash the tail of an axolotl larva with distilled water, place for an
hour in a watch-glassful of 0·25 per cent. solution of gold chloride,
containing 1 drop of hydrochloric acid; wash, and reduce in a mixture of 1
part of formic acid with 6 parts of water.
Mitrophanow’s Maceration Method for Epithelium.—Fix the embryo for
15 minutes in 3 per cent. nitric acid; then place for an hour in a mixture of
alcohol, 1 volume, and water 2 volumes, and finally treat with stronger
alcohol for 24 hours to separate the epidermis.
Müller’s Berlin Blue for Injections.—Precipitate a concentrated solution
of Berlin blue by means of 90 per cent. alcohol. The precipitate is very
finely divided, whilst the fluid is perfectly neutral and much easier to
prepare than that of Beale.
Neilsen’s Solution of Methyl Violet.—Dissolve fuchsine, 1 part, in
alcohol, 10 parts, and add a 5 per cent. watery solution of carbolic acid, 100
parts.
Neisser’s Double-Staining for Spore-Bearing Bacilli.—Cover-glass
preparations are immersed for 20 minutes in fuchsine aniline water
times as much water.
Merbel’s Carmine and Indigo Fluids (give a blue and red stain, and are
very selective).—To prepare the red fluid, take—Carmine, 2 dr.; borax, 2
dr.; distilled water, 4 ozs. For the blue fluid, take—Indigo carmine, 2 dr.;
borax, 2 dr.; distilled water, 4 ozs. Mix each in a mortar, and allow it to
stand, then pour off the supernatant fluid. If the sections have been
hardened in chromic acid, picric acid, or a bichromate, they must be washed
in water till no tinge appears. Place them in alcohol for fifteen or twenty
minutes, then in the two fluids mixed in equal proportions, after which
wash them in a saturated aqueous solution of oxalic acid, where they should
remain a rather shorter time than in the staining fluids. When sufficiently
bleached, wash them in water, to get rid of the acid, then pass them through
spirit and oil of cloves, and mount in balsam or dammar.
Mitrophanow’s Gold Process for Prickle-Cells and Intercellular
Canals.—Wash the tail of an axolotl larva with distilled water, place for an
hour in a watch-glassful of 0·25 per cent. solution of gold chloride,
containing 1 drop of hydrochloric acid; wash, and reduce in a mixture of 1
part of formic acid with 6 parts of water.
Mitrophanow’s Maceration Method for Epithelium.—Fix the embryo for
15 minutes in 3 per cent. nitric acid; then place for an hour in a mixture of
alcohol, 1 volume, and water 2 volumes, and finally treat with stronger
alcohol for 24 hours to separate the epidermis.
Müller’s Berlin Blue for Injections.—Precipitate a concentrated solution
of Berlin blue by means of 90 per cent. alcohol. The precipitate is very
finely divided, whilst the fluid is perfectly neutral and much easier to
prepare than that of Beale.
Neilsen’s Solution of Methyl Violet.—Dissolve fuchsine, 1 part, in
alcohol, 10 parts, and add a 5 per cent. watery solution of carbolic acid, 100
parts.
Neisser’s Double-Staining for Spore-Bearing Bacilli.—Cover-glass
preparations are immersed for 20 minutes in fuchsine aniline water
Page 795
(concentrated alcoholic solution of fuchsine, 11 C.c.; absolute alcohol, 10
C.c.; aniline water, 100 C.c.; then heat to 80° or 90° C.; next rinse in water,
alcohol, or weak acid, according to the nature of the bacilli, counterstain
with aqueous solution of methylene blue, rinse in water, dry and mount in
balsam). The spores are stained red and the rest of the bacilli blue.
Nissl’s Fuchsine Stain for Nerve Cells.—(1) Fresh material in pieces
measuring 1 C.c. are hardened in a “chromic solution in 70 per cent.
alcohol” for 2 days, then transferred to absolute alcohol for 5 days, and
afterwards cut. Stain the sections singly in a saturated solution of fuchsine,
warming in a deep watch-glass until vapours begin to be given off. Next
plunge the section into absolute alcohol for 1 or 2 minutes, then place it on
a slide, flood with clove oil, and when no more colour is given off, drain
and mount in balsam.
Ohlmacher’s Formaldehyde Staining.—Formalin in a 2 to 4 per cent.
solution is used as a mordant for tar colours. The tissues may be mordanted
separately by treatment for 1 minute or longer, or the formalin may be
added to the stain. Dissolve 1 Gm. of fuchsine in 10 C.c. of absolute
alcohol, and add to 100 C.c. of 4 per cent. formalin solution. Or, add
saturated alcoholic solution of gentian violet or methyl violet 5 B. to the
formalin solution, in the proportion of 1:10. In the case of methylene blue,
dissolve 1 G.m. in 100 C.c. of the formalin solution. Sections stain in half a
minute, and are said to resist alcohol much more than if formalin were not
used.
Oppitz’s Silver Staining.—Reduction is very rapidly effected by placing the
preparations for 2 or 3 minutes in a 0·25 to 0·5 per cent. solution of
chloride of tin.
Pal’s Hæmatoxylin Stain.—Dissolve 0·75 Gm. of hæmatoxylin in 90 C.c.
of distilled water and 10 C.c. of absolute alcohol. Just before use add
saturated solution of lithium carbonate in the proportion of 3 drops to each
10 C.c. of hæmatoxylin solution. (See Weigert.)
Pal’s Hæmatoxylin Method.—Proceed at first as in Weigert’s process for
nerve fibre, omitting the copper bath, and stain in Pal’s hæmatoxylin
solution (see above) for 5 or 6 hours. Then wash the sections in distilled
C.c.; aniline water, 100 C.c.; then heat to 80° or 90° C.; next rinse in water,
alcohol, or weak acid, according to the nature of the bacilli, counterstain
with aqueous solution of methylene blue, rinse in water, dry and mount in
balsam). The spores are stained red and the rest of the bacilli blue.
Nissl’s Fuchsine Stain for Nerve Cells.—(1) Fresh material in pieces
measuring 1 C.c. are hardened in a “chromic solution in 70 per cent.
alcohol” for 2 days, then transferred to absolute alcohol for 5 days, and
afterwards cut. Stain the sections singly in a saturated solution of fuchsine,
warming in a deep watch-glass until vapours begin to be given off. Next
plunge the section into absolute alcohol for 1 or 2 minutes, then place it on
a slide, flood with clove oil, and when no more colour is given off, drain
and mount in balsam.
Ohlmacher’s Formaldehyde Staining.—Formalin in a 2 to 4 per cent.
solution is used as a mordant for tar colours. The tissues may be mordanted
separately by treatment for 1 minute or longer, or the formalin may be
added to the stain. Dissolve 1 Gm. of fuchsine in 10 C.c. of absolute
alcohol, and add to 100 C.c. of 4 per cent. formalin solution. Or, add
saturated alcoholic solution of gentian violet or methyl violet 5 B. to the
formalin solution, in the proportion of 1:10. In the case of methylene blue,
dissolve 1 G.m. in 100 C.c. of the formalin solution. Sections stain in half a
minute, and are said to resist alcohol much more than if formalin were not
used.
Oppitz’s Silver Staining.—Reduction is very rapidly effected by placing the
preparations for 2 or 3 minutes in a 0·25 to 0·5 per cent. solution of
chloride of tin.
Pal’s Hæmatoxylin Stain.—Dissolve 0·75 Gm. of hæmatoxylin in 90 C.c.
of distilled water and 10 C.c. of absolute alcohol. Just before use add
saturated solution of lithium carbonate in the proportion of 3 drops to each
10 C.c. of hæmatoxylin solution. (See Weigert.)
Pal’s Hæmatoxylin Method.—Proceed at first as in Weigert’s process for
nerve fibre, omitting the copper bath, and stain in Pal’s hæmatoxylin
solution (see above) for 5 or 6 hours. Then wash the sections in distilled
Page 796
water (containing a trace of lithium carbonate if the sections are not deep
blue), next treat for 15 to 30 seconds with a 0·25 per cent. potassium
permanganate solution, rinse in water, and decolourise in Pal’s bleaching
solution. (If black spots appear replace in the permanganate solution, again
bleach, and wash for 15 minutes in water.) The grey substance of the
sections is decolourised in a few sections; the sections should then be well
washed out, and may be double-stained with picro-carmine or acetic acid
carmine (see Schneider), Magdala red, or eosine. The nuclei may be stained
with alum carmine. Finally dehydrate, clear, and mount.
Pal-Exner’s Osmic Acid Method.—Spinal cord or brain in 0·25 inch cubes
is immersed in 0·5 per cent. osmic acid solution for 2 days, the solution
being changed each day; then wash in water, transfer to absolute alcohol,
and imbed in celloidin or paraffin. Place sections as cut in glycerine, then
wash in water, treat with potassium permanganate and Pal’s solution, as in
Pal’s hæmatoxylin method, counter-stain with carmine, dehydrate, clear,
and mount in balsam.
Plant’s Method of Staining Actinomycosis.—Sections are placed for 10
minutes in Gibbes’ magenta solution or carbolic fuchsine, at 45° C.; next
they are rinsed in water and placed in saturated aqueous solution of picric
acid, mixed with an equal volume of absolute alcohol, for 5 or 10 minutes;
they are then washed once more, passed through 50 per cent. alcohol into
absolute alcohol, cleared in cedar oil, and mounted in balsam.
Ranvier’s Lemon Juice Method.—Soak pieces of fresh tissue in fresh
lemon juice until transparent (5 to 10 minutes), then rapidly wash in
distilled water, treat for 10 to 60 minutes with 1 per cent. gold chloride
solution, again wash and expose to light in a bottle containing 50 C.c. of
distilled water and 2 drops of acetic acid. Reduction is complete in 24 to 48
hours. If it is not desired to retain the superficial epithelium, reduction may
be more completely effected in the dark, by treatment with formic acid (sp.
gr. 1·2), diluted with 3 times its volume of water. The lemon juice in the
above process may be replaced by an aqueous solution of citric acid (40
grains in each ounce).
Ranvier’s Picro-Carmine.—Carmine, 1 part; distilled water, 10 parts;
solution of ammonia, 3 parts; mix and add of a cold saturated solution of
blue), next treat for 15 to 30 seconds with a 0·25 per cent. potassium
permanganate solution, rinse in water, and decolourise in Pal’s bleaching
solution. (If black spots appear replace in the permanganate solution, again
bleach, and wash for 15 minutes in water.) The grey substance of the
sections is decolourised in a few sections; the sections should then be well
washed out, and may be double-stained with picro-carmine or acetic acid
carmine (see Schneider), Magdala red, or eosine. The nuclei may be stained
with alum carmine. Finally dehydrate, clear, and mount.
Pal-Exner’s Osmic Acid Method.—Spinal cord or brain in 0·25 inch cubes
is immersed in 0·5 per cent. osmic acid solution for 2 days, the solution
being changed each day; then wash in water, transfer to absolute alcohol,
and imbed in celloidin or paraffin. Place sections as cut in glycerine, then
wash in water, treat with potassium permanganate and Pal’s solution, as in
Pal’s hæmatoxylin method, counter-stain with carmine, dehydrate, clear,
and mount in balsam.
Plant’s Method of Staining Actinomycosis.—Sections are placed for 10
minutes in Gibbes’ magenta solution or carbolic fuchsine, at 45° C.; next
they are rinsed in water and placed in saturated aqueous solution of picric
acid, mixed with an equal volume of absolute alcohol, for 5 or 10 minutes;
they are then washed once more, passed through 50 per cent. alcohol into
absolute alcohol, cleared in cedar oil, and mounted in balsam.
Ranvier’s Lemon Juice Method.—Soak pieces of fresh tissue in fresh
lemon juice until transparent (5 to 10 minutes), then rapidly wash in
distilled water, treat for 10 to 60 minutes with 1 per cent. gold chloride
solution, again wash and expose to light in a bottle containing 50 C.c. of
distilled water and 2 drops of acetic acid. Reduction is complete in 24 to 48
hours. If it is not desired to retain the superficial epithelium, reduction may
be more completely effected in the dark, by treatment with formic acid (sp.
gr. 1·2), diluted with 3 times its volume of water. The lemon juice in the
above process may be replaced by an aqueous solution of citric acid (40
grains in each ounce).
Ranvier’s Picro-Carmine.—Carmine, 1 part; distilled water, 10 parts;
solution of ammonia, 3 parts; mix and add of a cold saturated solution of
Page 797
picric acid 200 parts.
Renaut’s Hæmatoxylic Eosine.—Mix 30 C.c. of concentrated aqueous
solution of eosine, 40 C.c. of saturated alcoholic solution of hæmatoxylin
(which has been kept for some time and precipitated), and 130 C.c. of
saturated solution of potash alum in glycerine (sp. gr. 1·26). Stand for 5 or 6
weeks in a partially covered vessel, protected from dust, until the alcohol is
evaporated, and then filter. The filtrate can be diluted with glycerine if
desired. Mount objects in this fluid diluted with 1 or 2 volumes of
glycerine, or, stain separately for some days or weeks and mount in balsam,
after washing in alcohol charged with a sufficient quantity of eosine.
Ranvier and Vignal’s Osmium Mixture.—Fix tissues in a freshly-prepared
mixture of equal volumes of 1 per cent. osmic acid and 90 per cent. alcohol,
then wash out in 80 per cent. alcohol, next with water, and stain for 48
hours with picro-carmine or hæmatoxylin. This method has been applied to
the histology of insects.
Renaut’s Glycerine Hæmatoxylin.—To a saturated solution of potash alum
in glycerine, add a saturated solution of homatoxylin in 90 per cent. alcohol
drop by drop, so as to form a deeply coloured solution. Expose to daylight
for a week, and then filter. This solution, like Renaut’s hæmatoxylic cosine,
may be used for mounting unstained sections, which after some time absorb
the colour from the liquid and become stained.
Safranine.—Safranine, 0·5 Gm.; rectified spirit, 20 C.c.; distilled water, 80
C.c.
Schäfer’s Acid Logwood Solution is especially useful for certain
structures, as tendon, cells, &c. It is thus prepared:—A 1 per cent. solution
of acetic acid is coloured by the addition of 1·3 of its volume of logwood
solution.
Schäfer’s Aniline Dyes, whether in aqueous or alcoholic solutions, give
good results, and are prepared as follows:—Roseanilin or magenta (1 gr. to
1 oz. of alcohol), red; acetate of mauvein (4 gr., alcohol 1 oz., acid nitric 2
drops), blue; aniline black (2 gr., water 1 oz.), grey-black; Nicholson’s
soluble blue (1-6 gr., alcohol 1 oz., and nitric 2 m.), blue. These stains
Renaut’s Hæmatoxylic Eosine.—Mix 30 C.c. of concentrated aqueous
solution of eosine, 40 C.c. of saturated alcoholic solution of hæmatoxylin
(which has been kept for some time and precipitated), and 130 C.c. of
saturated solution of potash alum in glycerine (sp. gr. 1·26). Stand for 5 or 6
weeks in a partially covered vessel, protected from dust, until the alcohol is
evaporated, and then filter. The filtrate can be diluted with glycerine if
desired. Mount objects in this fluid diluted with 1 or 2 volumes of
glycerine, or, stain separately for some days or weeks and mount in balsam,
after washing in alcohol charged with a sufficient quantity of eosine.
Ranvier and Vignal’s Osmium Mixture.—Fix tissues in a freshly-prepared
mixture of equal volumes of 1 per cent. osmic acid and 90 per cent. alcohol,
then wash out in 80 per cent. alcohol, next with water, and stain for 48
hours with picro-carmine or hæmatoxylin. This method has been applied to
the histology of insects.
Renaut’s Glycerine Hæmatoxylin.—To a saturated solution of potash alum
in glycerine, add a saturated solution of homatoxylin in 90 per cent. alcohol
drop by drop, so as to form a deeply coloured solution. Expose to daylight
for a week, and then filter. This solution, like Renaut’s hæmatoxylic cosine,
may be used for mounting unstained sections, which after some time absorb
the colour from the liquid and become stained.
Safranine.—Safranine, 0·5 Gm.; rectified spirit, 20 C.c.; distilled water, 80
C.c.
Schäfer’s Acid Logwood Solution is especially useful for certain
structures, as tendon, cells, &c. It is thus prepared:—A 1 per cent. solution
of acetic acid is coloured by the addition of 1·3 of its volume of logwood
solution.
Schäfer’s Aniline Dyes, whether in aqueous or alcoholic solutions, give
good results, and are prepared as follows:—Roseanilin or magenta (1 gr. to
1 oz. of alcohol), red; acetate of mauvein (4 gr., alcohol 1 oz., acid nitric 2
drops), blue; aniline black (2 gr., water 1 oz.), grey-black; Nicholson’s
soluble blue (1-6 gr., alcohol 1 oz., and nitric 2 m.), blue. These stains
Page 798
should be used weak; and after sections are stained they should be passed
through alcohol and oil of cloves as rapidly as possible; otherwise the
colour will dissolve out before they can be mounted in balsam.
Schultze (Staining Bacilli).—Stain sections and cover-glass preparations
for some hours in aqueous methylene blue solution, differentiate in 0·5 per
cent. acetic acid, dehydrate in alcohol, clear in cedar oil, and mount in
balsam.
Sclavo’s Stain for Flagella.—Leave the preparations for 1 minute in a
solution of 1 Gm. of tannin in 100 C.c. of 50 per cent. alcohol; wash in
distilled water; transfer for 1 minute to 50 per cent. phospho-molybdic acid;
again wash, and stain for 3 to 5 minutes in a hot saturated solution of
fuchsine in aniline water. Then wash in water, dry on filter paper, and
mount in balsam.
Squire’s Picro-Carmine.—(1) Dissolve 1 Gm. of carmine with a gentle heat
in 3 C.c. of strong solution of ammonia, and 5 C.c. of distilled water, then
add 200 C.c. of saturated aqueous solution of picric acid, heat to boiling,
and filter. (2) Dissolve 10 Gm. of carmine in a solution of 1 Gm. of caustic
soda in 1000 C.c. of distilled water; boil, filter and make up to 1000 C.c.
with water. Mix the solution with an equal quantity of water, and add 1 per
cent. aqueous solution of picric acid so long as the turbidity produced
disappears on agitation.
Squire’s Blueing of Sections.—After staining with hæmatoxylin, treat for a
few seconds with a solution of sodium bicarbonate (1:1000) in distilled
water.
Valentine (Fuchsine).—Ether shaken with a solution containing fuchsine is
coloured violet after adding ferrous iodide, but not before.
Victoria Blue.—Victoria blue, 0·25 Gm.; rectified spirit, 20 C.c.; distilled
water, 80 C.c.
Wedl’s Orseille or Orchella Stain.—Mix 5 C.c. of acetic acid, 20 C.c. of
absolute alcohol, and 40 C.c. of distilled water; then add sufficient archil,
through alcohol and oil of cloves as rapidly as possible; otherwise the
colour will dissolve out before they can be mounted in balsam.
Schultze (Staining Bacilli).—Stain sections and cover-glass preparations
for some hours in aqueous methylene blue solution, differentiate in 0·5 per
cent. acetic acid, dehydrate in alcohol, clear in cedar oil, and mount in
balsam.
Sclavo’s Stain for Flagella.—Leave the preparations for 1 minute in a
solution of 1 Gm. of tannin in 100 C.c. of 50 per cent. alcohol; wash in
distilled water; transfer for 1 minute to 50 per cent. phospho-molybdic acid;
again wash, and stain for 3 to 5 minutes in a hot saturated solution of
fuchsine in aniline water. Then wash in water, dry on filter paper, and
mount in balsam.
Squire’s Picro-Carmine.—(1) Dissolve 1 Gm. of carmine with a gentle heat
in 3 C.c. of strong solution of ammonia, and 5 C.c. of distilled water, then
add 200 C.c. of saturated aqueous solution of picric acid, heat to boiling,
and filter. (2) Dissolve 10 Gm. of carmine in a solution of 1 Gm. of caustic
soda in 1000 C.c. of distilled water; boil, filter and make up to 1000 C.c.
with water. Mix the solution with an equal quantity of water, and add 1 per
cent. aqueous solution of picric acid so long as the turbidity produced
disappears on agitation.
Squire’s Blueing of Sections.—After staining with hæmatoxylin, treat for a
few seconds with a solution of sodium bicarbonate (1:1000) in distilled
water.
Valentine (Fuchsine).—Ether shaken with a solution containing fuchsine is
coloured violet after adding ferrous iodide, but not before.
Victoria Blue.—Victoria blue, 0·25 Gm.; rectified spirit, 20 C.c.; distilled
water, 80 C.c.
Wedl’s Orseille or Orchella Stain.—Mix 5 C.c. of acetic acid, 20 C.c. of
absolute alcohol, and 40 C.c. of distilled water; then add sufficient archil,
Page 799
from which excess of ammonia has been driven off, to form a dark reddish
fluid.
Weigert’s Hæmatoxylin.—Dissolve 1 part of hæmatoxylin in 10 parts of
absolute alcohol; then add 90 parts of distilled water and 1 part of aqueous
solution (1:70) of lithium carbonate.
Weigert (Gram’s Method).—In this modification aniline is substituted for
alcohol, in order to avoid prolonged washing with the latter, and the process
is conducted on a slide. The section is placed on a slide, stained with a few
drops of gentian violet aniline water, prepared as in Gram’s method, the
excess of fluid removed, and a few drops of Gram’s solution applied.
Subsequently remove the liquid by gently blotting it off, then wash the
section by allowing aniline to flow’ backwards and forwards over it, and
when colour ceases to come away, repeat the operation with xylol for about
1 minute, then mount in balsam.
Weigert (Staining in Actinomycosis).—Immerse sections for 1 hour in
Wedl’s Orseille stain, then quickly rinse with alcohol and counterstain with
gentian violet. If it be desired to stain the mycelium also, afterwards submit
the sections to Weigert’s modification of Gram’s method. See page 335.
Weigert (Staining Brain Tissue).—Pieces of brain and spinal cord are
hardened in bichromate solution, followed by alcohol, then imbedded in
celloidin or gum. If imbedded in celloidin, the pieces are subsequently
taken from the spirit in which they are immersed, and placed for one or two
days in saturated aqueous solution of copper acetate, diluted with an equal
bulk of water, the mixture being kept at about 40° C. Afterwards transfer
the pieces to 80 per cent. alcohol until required for cutting. Or, the sections
can be cut first, and then treated with copper acetate. To stain the sections,
after being well washed in 90 per cent. alcohol, they are transferred to
Weigert’s hæmatoxylin and left from a few hours to two days, according to
the differentiation required. When opaque and of a deep blue-black colour,
they should be well washed for two or three days in distilled water. Next
decolourise for 0·5 to 2 hours in a solution of 2 Gm. of borax and 2·5 Gm.
of potassium ferrocyanide in 200 C.c. of water. As soon as the grey and
white substances are sharply defined, again wash the sections in water for
half an hour, then dehydrate, clear, and mount in balsam.
fluid.
Weigert’s Hæmatoxylin.—Dissolve 1 part of hæmatoxylin in 10 parts of
absolute alcohol; then add 90 parts of distilled water and 1 part of aqueous
solution (1:70) of lithium carbonate.
Weigert (Gram’s Method).—In this modification aniline is substituted for
alcohol, in order to avoid prolonged washing with the latter, and the process
is conducted on a slide. The section is placed on a slide, stained with a few
drops of gentian violet aniline water, prepared as in Gram’s method, the
excess of fluid removed, and a few drops of Gram’s solution applied.
Subsequently remove the liquid by gently blotting it off, then wash the
section by allowing aniline to flow’ backwards and forwards over it, and
when colour ceases to come away, repeat the operation with xylol for about
1 minute, then mount in balsam.
Weigert (Staining in Actinomycosis).—Immerse sections for 1 hour in
Wedl’s Orseille stain, then quickly rinse with alcohol and counterstain with
gentian violet. If it be desired to stain the mycelium also, afterwards submit
the sections to Weigert’s modification of Gram’s method. See page 335.
Weigert (Staining Brain Tissue).—Pieces of brain and spinal cord are
hardened in bichromate solution, followed by alcohol, then imbedded in
celloidin or gum. If imbedded in celloidin, the pieces are subsequently
taken from the spirit in which they are immersed, and placed for one or two
days in saturated aqueous solution of copper acetate, diluted with an equal
bulk of water, the mixture being kept at about 40° C. Afterwards transfer
the pieces to 80 per cent. alcohol until required for cutting. Or, the sections
can be cut first, and then treated with copper acetate. To stain the sections,
after being well washed in 90 per cent. alcohol, they are transferred to
Weigert’s hæmatoxylin and left from a few hours to two days, according to
the differentiation required. When opaque and of a deep blue-black colour,
they should be well washed for two or three days in distilled water. Next
decolourise for 0·5 to 2 hours in a solution of 2 Gm. of borax and 2·5 Gm.
of potassium ferrocyanide in 200 C.c. of water. As soon as the grey and
white substances are sharply defined, again wash the sections in water for
half an hour, then dehydrate, clear, and mount in balsam.
Page 800
Woodhead’s Method of Staining Tubercle Bacilli.—Take a small quantity
of sputum rich in bacilli, and spread it out by pressure between two cover-
glasses, so that a fairly thin film remains on each. Then carefully slip one
over the other until they come apart. Thoroughly dry the covers, and pass
them rapidly three times through the flame of a spirit lamp, care being taken
not to scorch the film, then float them face downwards on the staining
solution, which has been previously prepared and filtered into a watch-
glass. The stain should consist of saturated alcoholic solution of basic
fuchsine, 1 part; absolute alcohol or rectified spirit, 10 parts; carbolic acid
solution (5 per cent.), 10 parts. Leave the preparations in the watch-glass for
12 to 24 hours, unless time is an object. In the latter case heat the fluid
gently until vapour is given off, then drop the films on the surface, and
leave them for 3 to 5 minutes only. Next transfer the covers to an aqueous
solution of sulphuric acid (25 per cent.), and when decolourisation is
complete, as evidenced by the pink colouration not returning when the
specimens are plunged into a bowl of tap-water containing a single drop of
ammonia solution, thoroughly rinse in the slightly alkaline water and
counter-stain in an aqueous solution of methylene blue. Finally, wash in
water, carefully dry and mount in Canada balsam. The bacilli should stand
out as bright red rods on a blue background of cells.
Ziehl-Neelsen (Staining Bacilli).—Sections are removed from weak spirit
into Neelsen’s carbolic fuchsine and left for 10 or 15 minutes; next
decolourise in sulphuric acid (sp. gr. 1·84) or nitric acid (sp. gr. 1·42)
diluted with 3 volumes of water, rinse in 60 per cent. alcohol, and wash in a
large volume of water to remove the acid. Tubercle and leprosy bacilli are
the only micro-organisms that can retain the stain after treatment with acid.
If the presence of traces of nitrous acid in the nitric acid be suspected,
Squire recommends the use of saturated aqueous solution of sulphanilic
acid mixed with one-third its bulk of nitric acid. The sulphanilic acid
destroys any free nitrous acid, which would otherwise exercise a bleaching
action on the fuchsine-stained bacilli. The sections may be counterstained
with a solution of 0·5 Gm. of methyl green (or 0·25 Gm. of methylene blue)
in 20 C.c. of rectified spirit and 80 C.c. of distilled water. Finally dehydrate
in absolute alcohol, clear in cedar oil, and mount in balsam.
of sputum rich in bacilli, and spread it out by pressure between two cover-
glasses, so that a fairly thin film remains on each. Then carefully slip one
over the other until they come apart. Thoroughly dry the covers, and pass
them rapidly three times through the flame of a spirit lamp, care being taken
not to scorch the film, then float them face downwards on the staining
solution, which has been previously prepared and filtered into a watch-
glass. The stain should consist of saturated alcoholic solution of basic
fuchsine, 1 part; absolute alcohol or rectified spirit, 10 parts; carbolic acid
solution (5 per cent.), 10 parts. Leave the preparations in the watch-glass for
12 to 24 hours, unless time is an object. In the latter case heat the fluid
gently until vapour is given off, then drop the films on the surface, and
leave them for 3 to 5 minutes only. Next transfer the covers to an aqueous
solution of sulphuric acid (25 per cent.), and when decolourisation is
complete, as evidenced by the pink colouration not returning when the
specimens are plunged into a bowl of tap-water containing a single drop of
ammonia solution, thoroughly rinse in the slightly alkaline water and
counter-stain in an aqueous solution of methylene blue. Finally, wash in
water, carefully dry and mount in Canada balsam. The bacilli should stand
out as bright red rods on a blue background of cells.
Ziehl-Neelsen (Staining Bacilli).—Sections are removed from weak spirit
into Neelsen’s carbolic fuchsine and left for 10 or 15 minutes; next
decolourise in sulphuric acid (sp. gr. 1·84) or nitric acid (sp. gr. 1·42)
diluted with 3 volumes of water, rinse in 60 per cent. alcohol, and wash in a
large volume of water to remove the acid. Tubercle and leprosy bacilli are
the only micro-organisms that can retain the stain after treatment with acid.
If the presence of traces of nitrous acid in the nitric acid be suspected,
Squire recommends the use of saturated aqueous solution of sulphanilic
acid mixed with one-third its bulk of nitric acid. The sulphanilic acid
destroys any free nitrous acid, which would otherwise exercise a bleaching
action on the fuchsine-stained bacilli. The sections may be counterstained
with a solution of 0·5 Gm. of methyl green (or 0·25 Gm. of methylene blue)
in 20 C.c. of rectified spirit and 80 C.c. of distilled water. Finally dehydrate
in absolute alcohol, clear in cedar oil, and mount in balsam.
Page 801
Appendix D.
THE METRIC SYSTEM OF WEIGHTS AND MEASURES.
The initial unit of the Metric System is the Metre or unit of length, which
represents one ten millionth part of the earth’s quadrant, or one forty-
millionth part of the circumference of the earth around the poles. The
multiples and sub-divisions of this and all the other units are obtained by
the use of decimals, and for this reason the system is also known as the
decimal system. The multiples are designated by the Greek prefixes, deca =
10; hecto = 100; kilo = 1000; myria = 10,000. For the sub-divisions Latin
prefixes are employed, as follows: deci = 1⁄10; centi = 1⁄100; milli = 1⁄1000. Thus
for measures of length we have the following expressions, showing the
abbreviations commonly employed, and the equivalents in the ordinary
English standards of measurement—
1 Myriametre, Mm. = 10,000.0 M. = 6.2137 miles.
1 Kilometre, Km. = 1,000.0 M. = 0.6213 mile.
1 Hectometre, Hm. = 100.0 M. = 109.362 yards.
1 Decametre, Dm. = 10.0 M. = 32.8086 feet.
1 Metre, M. = 1.0 M. = 39.3704 inches.
1 Decimetre, dm. = 0.1 M. = 3.9370 "
1 Centimetre, cm. = 0.01 M. = 0.3937 "
1 Millimetre, mm. = 0.001 M. = 0.0393 "
From the unit of linear measure of metre is derived the unit of the measure
of capacity or Litre. This represents the cube of one-tenth part of a metre,
or a cubic decimetre, and its multiples and sub-divisions with their
corresponding equivalents in Imperial fluid measure are as follows:—
imperial
1 Myrialitre, Ml. = 10,000.0 L. = 2200.9667
gallons.91
1 Kilolitre, Kl. = 1,000.0 " = 220.0966 imperial gallons.
1 Hectolitre Hl. = 100.0 " = 22.0096 imperial gallons.
1 Decalitre, Dl. = 10.0 " = 2.2009 imperial gallons.
THE METRIC SYSTEM OF WEIGHTS AND MEASURES.
The initial unit of the Metric System is the Metre or unit of length, which
represents one ten millionth part of the earth’s quadrant, or one forty-
millionth part of the circumference of the earth around the poles. The
multiples and sub-divisions of this and all the other units are obtained by
the use of decimals, and for this reason the system is also known as the
decimal system. The multiples are designated by the Greek prefixes, deca =
10; hecto = 100; kilo = 1000; myria = 10,000. For the sub-divisions Latin
prefixes are employed, as follows: deci = 1⁄10; centi = 1⁄100; milli = 1⁄1000. Thus
for measures of length we have the following expressions, showing the
abbreviations commonly employed, and the equivalents in the ordinary
English standards of measurement—
1 Myriametre, Mm. = 10,000.0 M. = 6.2137 miles.
1 Kilometre, Km. = 1,000.0 M. = 0.6213 mile.
1 Hectometre, Hm. = 100.0 M. = 109.362 yards.
1 Decametre, Dm. = 10.0 M. = 32.8086 feet.
1 Metre, M. = 1.0 M. = 39.3704 inches.
1 Decimetre, dm. = 0.1 M. = 3.9370 "
1 Centimetre, cm. = 0.01 M. = 0.3937 "
1 Millimetre, mm. = 0.001 M. = 0.0393 "
From the unit of linear measure of metre is derived the unit of the measure
of capacity or Litre. This represents the cube of one-tenth part of a metre,
or a cubic decimetre, and its multiples and sub-divisions with their
corresponding equivalents in Imperial fluid measure are as follows:—
imperial
1 Myrialitre, Ml. = 10,000.0 L. = 2200.9667
gallons.91
1 Kilolitre, Kl. = 1,000.0 " = 220.0966 imperial gallons.
1 Hectolitre Hl. = 100.0 " = 22.0096 imperial gallons.
1 Decalitre, Dl. = 10.0 " = 2.2009 imperial gallons.
Page 802
fluid ounces
1 Litre, L. = 1.0 " = 35.2154
imperial.
fluid ounces
1 Decilitre, dl. = 0.1 " = 3.5215
imperial.
fluid ounces
1 Centilitre, cl. = 0.01 " = 0.3521
imperial.
fluid ounces
1 Millilitre, ml. = 0.001 " = 0.0352
imperial.
or
Cubic fluid ounces
1 ccm. = 0.001 L. = 0.0352
Centimetre, imperial.
The unit of weight in the metric system is the Gramme. This is also derived
from the metre, and represents the weight of one cubic centimetre, of water,
or the quantity of distilled water, at its maximum density, 4° C. (39·2° F.),
which would fill the cube of one-hundredth part of a metre. The relative
value of the gramme, together with its multiples and sub-divisions, as
compared with the English standards of weight, may be seen from the
following table:—
Gm.
1 Myriagramme, Mg. = 10,000.0 22.0461 pounds.
=
1 Kilogramme, Kg. = 1,000.0 " = 2.2046 "
ounces
1 Hectogramme, Hg. = 100.0 " = 3.5273
avoir.
1 Decagramme, Dg. = 10.0 " = 154.3235 grains.
1 Gramme, Gm. = 1.0 " = 15.4323 "
1 Decigramme, dg. = 0.1 " = 1.5432 "
1 Centigramme, cg. = 0.01 " = 0.1543 "
1 Milligramme, mg. = 0.001 " = 0.0154 "
The expression micro-millimetre is used for microscopic measurements, and
denotes the thousandth part of a millimetre. Of the measures of capacity, the
terms most commonly employed are the litre and the cubic centimetre. Thus
a decalitre may also be expressed as 10 litres, a centilitre as 10 cubic
centimetres, etc. Of the metric weights the gramme and its fractional parts,
1 Litre, L. = 1.0 " = 35.2154
imperial.
fluid ounces
1 Decilitre, dl. = 0.1 " = 3.5215
imperial.
fluid ounces
1 Centilitre, cl. = 0.01 " = 0.3521
imperial.
fluid ounces
1 Millilitre, ml. = 0.001 " = 0.0352
imperial.
or
Cubic fluid ounces
1 ccm. = 0.001 L. = 0.0352
Centimetre, imperial.
The unit of weight in the metric system is the Gramme. This is also derived
from the metre, and represents the weight of one cubic centimetre, of water,
or the quantity of distilled water, at its maximum density, 4° C. (39·2° F.),
which would fill the cube of one-hundredth part of a metre. The relative
value of the gramme, together with its multiples and sub-divisions, as
compared with the English standards of weight, may be seen from the
following table:—
Gm.
1 Myriagramme, Mg. = 10,000.0 22.0461 pounds.
=
1 Kilogramme, Kg. = 1,000.0 " = 2.2046 "
ounces
1 Hectogramme, Hg. = 100.0 " = 3.5273
avoir.
1 Decagramme, Dg. = 10.0 " = 154.3235 grains.
1 Gramme, Gm. = 1.0 " = 15.4323 "
1 Decigramme, dg. = 0.1 " = 1.5432 "
1 Centigramme, cg. = 0.01 " = 0.1543 "
1 Milligramme, mg. = 0.001 " = 0.0154 "
The expression micro-millimetre is used for microscopic measurements, and
denotes the thousandth part of a millimetre. Of the measures of capacity, the
terms most commonly employed are the litre and the cubic centimetre. Thus
a decalitre may also be expressed as 10 litres, a centilitre as 10 cubic
centimetres, etc. Of the metric weights the gramme and its fractional parts,
Page 803
with their respective prefixes, are much used in analytical work. The
kilogramme is largely employed in commercial transactions, and is
commonly abbreviated kilo.
As a comparison of the values of some of the more frequently employed
expressions of the metric and English systems, the following may be found
convenient for reference:—
1 mm. (millimetre) = 1⁄25 of an inch.
1 cm. (centimetre) = 2⁄5 of an inch.
1 inch = 25 millimetres or 2½ centimetres.
1 mg. (milligramme) = 0.01543 grain (or approx. 1⁄64 grain).
1 gm. (gramme) = 15.4324 grains.
1 Kg. (“Kilo” or kilogramme) = 2 lbs. 3¼ ozs. av.
1 pound avoir. = 453,592 grammes.
1 ounce avoir. = 28,350 grammes.
1 grain = 0.06479 gramme or 64.79 milligrammes.
1 cc. (cubic centimetre) = 16.9 minims Imperial measure.
1 L. (litre) = 35.21 fluid ounces Imperial measure, or 33.815 fluid ounces
Wine measure.
1 fluid ounce Imperial measure = 28.350 grammes.
1 pint Imperial measure = 567.0 grammes.
1 gallon Imperial measure = 4.536 litres, or 10 lbs. avoir. of pure water at
62° F. and under an atmospheric pressure of 30 inches of mercury.
It may be well to bear in mind that on the Continent liquids are always
weighed, not measured.
Appendix E.
COMPARISON BETWEEN THE CENTIGRADE AND FAHRENHEIT
THERMOMETERS.
F. C. F. C.
kilogramme is largely employed in commercial transactions, and is
commonly abbreviated kilo.
As a comparison of the values of some of the more frequently employed
expressions of the metric and English systems, the following may be found
convenient for reference:—
1 mm. (millimetre) = 1⁄25 of an inch.
1 cm. (centimetre) = 2⁄5 of an inch.
1 inch = 25 millimetres or 2½ centimetres.
1 mg. (milligramme) = 0.01543 grain (or approx. 1⁄64 grain).
1 gm. (gramme) = 15.4324 grains.
1 Kg. (“Kilo” or kilogramme) = 2 lbs. 3¼ ozs. av.
1 pound avoir. = 453,592 grammes.
1 ounce avoir. = 28,350 grammes.
1 grain = 0.06479 gramme or 64.79 milligrammes.
1 cc. (cubic centimetre) = 16.9 minims Imperial measure.
1 L. (litre) = 35.21 fluid ounces Imperial measure, or 33.815 fluid ounces
Wine measure.
1 fluid ounce Imperial measure = 28.350 grammes.
1 pint Imperial measure = 567.0 grammes.
1 gallon Imperial measure = 4.536 litres, or 10 lbs. avoir. of pure water at
62° F. and under an atmospheric pressure of 30 inches of mercury.
It may be well to bear in mind that on the Continent liquids are always
weighed, not measured.
Appendix E.
COMPARISON BETWEEN THE CENTIGRADE AND FAHRENHEIT
THERMOMETERS.
F. C. F. C.
Page 804
212 100 86 30
200 93.3 84 28.9
150 65.6 82 27.8
112 44.4 80 26.7
110 43.3 78 25.6
108 42.2 76 24.4
106 41.1 74 23.3
105 40.5 72 22.2
104 40 70 21.1
103 39.4 68 20
102 38.9 66 18.9
101 38.3 64 17.8
100 37.8 62 16.7
99 37.2 60 15.6
98 36.7 58 14.4
96 35.6 56 13.3
94 34.4 54 12.2
92 33.3 52 11.1
90 32.2 32 0
88 31.1 25 -3.9
200 93.3 84 28.9
150 65.6 82 27.8
112 44.4 80 26.7
110 43.3 78 25.6
108 42.2 76 24.4
106 41.1 74 23.3
105 40.5 72 22.2
104 40 70 21.1
103 39.4 68 20
102 38.9 66 18.9
101 38.3 64 17.8
100 37.8 62 16.7
99 37.2 60 15.6
98 36.7 58 14.4
96 35.6 56 13.3
94 34.4 54 12.2
92 33.3 52 11.1
90 32.2 32 0
88 31.1 25 -3.9
Page 805
Dr. Culpeper’s Microscope 1738.
Page 806
INDEX.
Abbé on microscopical vision, 37
Abbé’s apertometer, 59
—— condenser, 176
—— stereoscopic eye-pieces, 64
—— test-plate, 164
Aberration, chromatic, 25
—— of the eye, chromatic, 33
—— spherical, 23
Abraxas grossulariata, 598
Absolute alcohol as a hardening reagent, 287
Acaras domesticus, 625
Accessories of the microscope, 197
Achromatic condenser, Beck’s, 180
—— —— Gillett’s, 173
—— —— method of using, 190
—— —— Powell’s, 178
—— —— Ross’s, 176
—— —— Smith & Beck’s, 173
—— —— Watson’s, 177
Achromatic objective, the, 152
Acineta, 495
Actiniæ, 527
Actinophrys-sol, 489
Adams’s book on the microscope, 8
Adipose tissue, 644
Ædogoniaceæ, 409
Aerobic spores, 399
Agar-agar, to prepare nutrient, 330
Air bubbles, 348
Alcyonella, 534
Abbé on microscopical vision, 37
Abbé’s apertometer, 59
—— condenser, 176
—— stereoscopic eye-pieces, 64
—— test-plate, 164
Aberration, chromatic, 25
—— of the eye, chromatic, 33
—— spherical, 23
Abraxas grossulariata, 598
Absolute alcohol as a hardening reagent, 287
Acaras domesticus, 625
Accessories of the microscope, 197
Achromatic condenser, Beck’s, 180
—— —— Gillett’s, 173
—— —— method of using, 190
—— —— Powell’s, 178
—— —— Ross’s, 176
—— —— Smith & Beck’s, 173
—— —— Watson’s, 177
Achromatic objective, the, 152
Acineta, 495
Actiniæ, 527
Actinophrys-sol, 489
Adams’s book on the microscope, 8
Adipose tissue, 644
Ædogoniaceæ, 409
Aerobic spores, 399
Agar-agar, to prepare nutrient, 330
Air bubbles, 348
Alcyonella, 534
Page 807
Algæ, 399
—— media for preserving, 343
—— red, 413
Alvarez’s discovery of bacillus, 392
Amici prism, the, 190
Amœba, 480
Amphibian changes, 669
Amphistoma, 570
Amyot finder, the, 205
Anacharis alsinastrum, 419
Anemones, sea, 526
Angle of vision, 72
Anguillula, 567
Animal structures, staining, 292
Annulosa, 562
Antennæ of insects, 584
Antenna of silkworm moth, 605
Anthrax bacillus, 369
Anthrozoa, 523
Apertometer, Abbé’s, 59
Aperture, definition of, 45
—— measurement of, 57
—— numerical, 57
—— table, 58
Aphides, 587
Aphrophora bifasciata, 618
Apis mellifica, 598
Aplysiidæ, 549
—— dipilans, 549
Apparatus for mounting, 352
Appendices, 673
Arachnidæ, 618
Aragonite, 232
Arcella, 483
Arenicola, 577
Argyroneta aquatica, 621
Artemiæ, 581
—— media for preserving, 343
—— red, 413
Alvarez’s discovery of bacillus, 392
Amici prism, the, 190
Amœba, 480
Amphibian changes, 669
Amphistoma, 570
Amyot finder, the, 205
Anacharis alsinastrum, 419
Anemones, sea, 526
Angle of vision, 72
Anguillula, 567
Animal structures, staining, 292
Annulosa, 562
Antennæ of insects, 584
Antenna of silkworm moth, 605
Anthrax bacillus, 369
Anthrozoa, 523
Apertometer, Abbé’s, 59
Aperture, definition of, 45
—— measurement of, 57
—— numerical, 57
—— table, 58
Aphides, 587
Aphrophora bifasciata, 618
Apis mellifica, 598
Aplysiidæ, 549
—— dipilans, 549
Apparatus for mounting, 352
Appendices, 673
Arachnidæ, 618
Aragonite, 232
Arcella, 483
Arenicola, 577
Argyroneta aquatica, 621
Artemiæ, 581
Page 808
Arteries, 622
Artery-needle, 303
Arthropoda, 583
Arthrospores, 366
Ascidian, 669
Astroides calyculcaris, 529
Babè’s method of staining bacteria, 334
Bacillus, anthrax, 369
—— of plague, 372
—— —— in rat’s blood, 372
—— splenic fever, 369
—— typhoid, 370
Bacteria, 317
—— aerobic, 399
—— classification of, 373
—— Cohn on multiplication of, 367
—— cultivation of, 327
—— —— in tubes, 331
—— —— on plates, 331
—— faculties of, 373
—— in butter, 393
—— in cheese, 393
—— in milk, 393
—— in sections of tissue, 337
—— invasion of potato-tubers by, 398
—— microscopical examination of, 333
—— phosphorescent, 373
—— reproduction of, 365
—— size of, 365
—— staining, 334
—— Winogradsky’s investigations of, 398
Bacterial action in tanning skins, 393
—— fermentations, 391
Bacteriological investigations, apparatus for, 318
—— —— mounting media, 320
Artery-needle, 303
Arthropoda, 583
Arthrospores, 366
Ascidian, 669
Astroides calyculcaris, 529
Babè’s method of staining bacteria, 334
Bacillus, anthrax, 369
—— of plague, 372
—— —— in rat’s blood, 372
—— splenic fever, 369
—— typhoid, 370
Bacteria, 317
—— aerobic, 399
—— classification of, 373
—— Cohn on multiplication of, 367
—— cultivation of, 327
—— —— in tubes, 331
—— —— on plates, 331
—— faculties of, 373
—— in butter, 393
—— in cheese, 393
—— in milk, 393
—— in sections of tissue, 337
—— invasion of potato-tubers by, 398
—— microscopical examination of, 333
—— phosphorescent, 373
—— reproduction of, 365
—— size of, 365
—— staining, 334
—— Winogradsky’s investigations of, 398
Bacterial action in tanning skins, 393
—— fermentations, 391
Bacteriological investigations, apparatus for, 318
—— —— mounting media, 320
Page 809
—— —— reagents used, 320
—— microscope, the, 135
Bacteriology of the dairy, 393
Baker’s advanced student’s microscope, 123
—— collecting stick, 350
—— histological microscope, 125
—— micro-photographic apparatus, 217
—— microscope lamp, 191
—— microscopes, 120
—— Nelson condenser, 184
—— —— model microscope, 120
—— objectives, 168
—— student’s condenser, 184
Baird, Dr., on daphnia, 581
Barnacle, 539
Bartley’s warm-stage, 281
Batrachospermæ, 409
Beck’s binocular dissecting microscope, 101
—— —— National microscope, 99
—— complete microscope lamp, 202
—— compressor, 275
—— disc-holder, 198
—— large Continental model microscope, 98
—— microscopes, 95
—— objectives, 167
—— pathological microscope, 95
—— Star microscope, 101
Beggiatoa, 400
Benjamin Martin’s microscope, 5
Beroidæ, 519
Biaxial crystals, 228
Bilharzia hæmatobra, 573
Binocular microscope, advantage of, 69
—— —— Carpenter on, 69
—— —— Nachet’s, 62
—— —— Pillischer’s, 128
—— —— Riddell’s, 62
—— microscope, the, 135
Bacteriology of the dairy, 393
Baker’s advanced student’s microscope, 123
—— collecting stick, 350
—— histological microscope, 125
—— micro-photographic apparatus, 217
—— microscope lamp, 191
—— microscopes, 120
—— Nelson condenser, 184
—— —— model microscope, 120
—— objectives, 168
—— student’s condenser, 184
Baird, Dr., on daphnia, 581
Barnacle, 539
Bartley’s warm-stage, 281
Batrachospermæ, 409
Beck’s binocular dissecting microscope, 101
—— —— National microscope, 99
—— complete microscope lamp, 202
—— compressor, 275
—— disc-holder, 198
—— large Continental model microscope, 98
—— microscopes, 95
—— objectives, 167
—— pathological microscope, 95
—— Star microscope, 101
Beggiatoa, 400
Benjamin Martin’s microscope, 5
Beroidæ, 519
Biaxial crystals, 228
Bilharzia hæmatobra, 573
Binocular microscope, advantage of, 69
—— —— Carpenter on, 69
—— —— Nachet’s, 62
—— —— Pillischer’s, 128
—— —— Riddell’s, 62
Page 810
—— —— Stephenson’s erecting, 71
—— —— Wenham’s, 65
—— vision, 60
Bismarck-brown for staining protoplasm, 306
Bivalves, 538
Bleaching process, 315
Blood as a test, 263
—— circulation of, in frog’s foot, 665
—— —— —— tadpole, 665
—— corpuscles, 638
—— —— double staining, 295
—— —— size of, 640
—— crystals, 641
—— spectrum, 252
Bombay plague, 371
Bone, 658
—— of fish, 661
—— of reptilia, 660
—— structure of, 659
Borax, 231
Boring sponges, 513
Botterill’s live-trough, 276
Brachiopoda, 538
Branchipodidæ, 580
Brewster’s microscope, 11
Brittleworts, 427
Browning-Huggins micro-spectroscope, 245
Browning’s pocket lens, 76
Bryophyta, 444
Bryozoa, 531
Buchner’s experiments on yeast, 389
Bull’s-eye condensing-lens, 199
Butter, bacteria in, 393
Butterfly’s tongue, 605
—— wings, 610
—— —— Wenham’s, 65
—— vision, 60
Bismarck-brown for staining protoplasm, 306
Bivalves, 538
Bleaching process, 315
Blood as a test, 263
—— circulation of, in frog’s foot, 665
—— —— —— tadpole, 665
—— corpuscles, 638
—— —— double staining, 295
—— —— size of, 640
—— crystals, 641
—— spectrum, 252
Bombay plague, 371
Bone, 658
—— of fish, 661
—— of reptilia, 660
—— structure of, 659
Borax, 231
Boring sponges, 513
Botterill’s live-trough, 276
Brachiopoda, 538
Branchipodidæ, 580
Brewster’s microscope, 11
Brittleworts, 427
Browning-Huggins micro-spectroscope, 245
Browning’s pocket lens, 76
Bryophyta, 444
Bryozoa, 531
Buchner’s experiments on yeast, 389
Bull’s-eye condensing-lens, 199
Butter, bacteria in, 393
Butterfly’s tongue, 605
—— wings, 610
Page 811
Calc-spar, 231
Cambridge rocking microtome, 290
Camera lucida, the, 207
—— —— the Abbé, 208
—— —— the Wollaston, 207
—— Swift’s horizontal, 213
Canada balsam, 293
Carbonate of lead, 232
Carmine as a nuclear stain, 312
Cartilage, 655
Catheart’s freezing microtome, 291
Cedar oil, use of, 171
Cell, definition of, 358
Cell-making turn-table, Walmsley’s 340
Cells, epithelial, 636
—— for living objects, 276
—— for mounting, 340
—— live, 277
Cellulose, 357
—— staining, 314
Cements, 347
—— list of, 676
Centipedes, 578
Cercariæ, 571
Cereal parasites, 381
Chætophoraceæ, 409
Chara, fructification of, 417
—— mounting, 347
—— vulgaris, 415
Characeæ, 415
Cheese, bacteria in, 393
—— mite, 625
Chilinidæ, 551
Chitonidæ, 545
Chloride of gold as stain, 297
—— of palladium as stain, 298
Chromatic aberration, 25
Cambridge rocking microtome, 290
Camera lucida, the, 207
—— —— the Abbé, 208
—— —— the Wollaston, 207
—— Swift’s horizontal, 213
Canada balsam, 293
Carbonate of lead, 232
Carmine as a nuclear stain, 312
Cartilage, 655
Catheart’s freezing microtome, 291
Cedar oil, use of, 171
Cell, definition of, 358
Cell-making turn-table, Walmsley’s 340
Cells, epithelial, 636
—— for living objects, 276
—— for mounting, 340
—— live, 277
Cellulose, 357
—— staining, 314
Cements, 347
—— list of, 676
Centipedes, 578
Cercariæ, 571
Cereal parasites, 381
Chætophoraceæ, 409
Chara, fructification of, 417
—— mounting, 347
—— vulgaris, 415
Characeæ, 415
Cheese, bacteria in, 393
—— mite, 625
Chilinidæ, 551
Chitonidæ, 545
Chloride of gold as stain, 297
—— of palladium as stain, 298
Chromatic aberration, 25
Page 812
—— —— of the eye, 33
Chromic acid as hardening reagent, 288
Ciliata, 498
Circulation of the blood, 665
Cistula catenata, 558
Cladocera, 580
Clavatella prolifera, 521
Clearing agents, list of, 676
Clepsinidæ, 576
Clionæ, 513
Closterium, 424
—— lunula, 425
Cnidaria, 519
Cockchafer’s eye, 590
Coddington lens, the, 76
Codosiga, 497
Cœlenterata, 515
Cohn on multiplication of bacteria, 367
Cole’s direction for section cutting, 285
—— section-cutting microtome, 289
Collecting stick, Baker’s, 350
Collection of objects, 349
Compound microscope, 78
Compressor, Beck’s, 275
Compressorium, 274
—— Ross’s, 275
—— Rousselet’s, 275
Concave lenses, 23
—— surfaces, 17
Condenser, Abbé’s, 176
—— Baker’s Nelson, 184
—— —— student’s, 184
—— Beck’s achromatic, 180
—— Gillett’s achromatic, 173
—— method of using, 190
—— Powell’s achromatic, 178
—— Ross’s achromatic, 176
Chromic acid as hardening reagent, 288
Ciliata, 498
Circulation of the blood, 665
Cistula catenata, 558
Cladocera, 580
Clavatella prolifera, 521
Clearing agents, list of, 676
Clepsinidæ, 576
Clionæ, 513
Closterium, 424
—— lunula, 425
Cnidaria, 519
Cockchafer’s eye, 590
Coddington lens, the, 76
Codosiga, 497
Cœlenterata, 515
Cohn on multiplication of bacteria, 367
Cole’s direction for section cutting, 285
—— section-cutting microtome, 289
Collecting stick, Baker’s, 350
Collection of objects, 349
Compound microscope, 78
Compressor, Beck’s, 275
Compressorium, 274
—— Ross’s, 275
—— Rousselet’s, 275
Concave lenses, 23
—— surfaces, 17
Condenser, Abbé’s, 176
—— Baker’s Nelson, 184
—— —— student’s, 184
—— Beck’s achromatic, 180
—— Gillett’s achromatic, 173
—— method of using, 190
—— Powell’s achromatic, 178
—— Ross’s achromatic, 176
Page 813
—— Smith & Beck’s achromatic, 173
—— —— substage, 193
Condenser, Swift’s, 183
—— Watson’s achromatic, 177
—— —— parachromatic, 182
—— Webster-Collins, 186
—— Wenham’s immersion, 189
—— —— parabolic, 186
Confervaceæ, 408
Conjugate foci, 17
—— real and virtual, 21
Continental microscopes, 130
Contrast stains, 313
Convex lens, 18
Copepoda, 580
Corals, 515, 525
—— true, 528
—— typical forms of, 533
Correction collar, Lister’s, 155
Coryne stauridia, 534
Cotton fibres, 474
Cover glass gauge, Zeiss’s, 165
Crinoids, 542
Critical angle, 14
Crookshank’s incubator, 324
—— method of staining bacteria, 335
Crustaceæ, 578
Crystals, formation and polarisation of, 239
Ctenophora, 518
Cuckoo-spit, 618
Culex pipiens, 596
Cultivation of bacteria, 327
—— of micro-organisms, 327
Cutleria dichotoma, 413
Cutting sections of hard woods, 316
Cuttle-fish, 556
Cyclops, 580
—— —— substage, 193
Condenser, Swift’s, 183
—— Watson’s achromatic, 177
—— —— parachromatic, 182
—— Webster-Collins, 186
—— Wenham’s immersion, 189
—— —— parabolic, 186
Confervaceæ, 408
Conjugate foci, 17
—— real and virtual, 21
Continental microscopes, 130
Contrast stains, 313
Convex lens, 18
Copepoda, 580
Corals, 515, 525
—— true, 528
—— typical forms of, 533
Correction collar, Lister’s, 155
Coryne stauridia, 534
Cotton fibres, 474
Cover glass gauge, Zeiss’s, 165
Crinoids, 542
Critical angle, 14
Crookshank’s incubator, 324
—— method of staining bacteria, 335
Crustaceæ, 578
Crystals, formation and polarisation of, 239
Ctenophora, 518
Cuckoo-spit, 618
Culex pipiens, 596
Cultivation of bacteria, 327
—— of micro-organisms, 327
Cutleria dichotoma, 413
Cutting sections of hard woods, 316
Cuttle-fish, 556
Cyclops, 580
Page 814
Cyclosis, phenomenon of, 359
Cyclostomata, 537
Cyclotus translucidus, 558
Cydippidæ, 518
Cymba olla, 557
Cymothordæ, 580
Dairy, bacteriology of, 393
Daphnia, enemies of, 581
—— ephippial eggs of, 580
Daphnia pulex, 580
De Bary’s investigations in parasitism, 395
Decalcifying and bleaching agents, list of, 677
Decalcifying solution as hardening reagent, 288
Demodex folliculorum, 627
Dental structure, 652
Dermestes lardarius, 627
Dermis, the human, 647
Desmidiaceæ, 420
—— reproduction of, 423
Diamond microscope, Pritchard’s, 9
Diaphragm, the, 194
—— the iris, 176
Diatomaceæ, 420, 427
—— fossilised, 437
—— Max Schultze’s researches, 430
—— where found, 428
Diatoms, mounting medium, 343
—— movements of, 431
Didymoprium grevelli, 420
Difflugia, 482
Digestive system of insects, 587
Dipping-tubes, 279
Disc-holder, Beck’s, 198
Dissecting-knives, 284
Dog-tick, 624
Cyclostomata, 537
Cyclotus translucidus, 558
Cydippidæ, 518
Cymba olla, 557
Cymothordæ, 580
Dairy, bacteriology of, 393
Daphnia, enemies of, 581
—— ephippial eggs of, 580
Daphnia pulex, 580
De Bary’s investigations in parasitism, 395
Decalcifying and bleaching agents, list of, 677
Decalcifying solution as hardening reagent, 288
Demodex folliculorum, 627
Dental structure, 652
Dermestes lardarius, 627
Dermis, the human, 647
Desmidiaceæ, 420
—— reproduction of, 423
Diamond microscope, Pritchard’s, 9
Diaphragm, the, 194
—— the iris, 176
Diatomaceæ, 420, 427
—— fossilised, 437
—— Max Schultze’s researches, 430
—— where found, 428
Diatoms, mounting medium, 343
—— movements of, 431
Didymoprium grevelli, 420
Difflugia, 482
Digestive system of insects, 587
Dipping-tubes, 279
Disc-holder, Beck’s, 198
Dissecting-knives, 284
Dog-tick, 624
Page 815
Double convex lens, 19
Draparnaldia glomerata, 409
Draw-tube, Swift’s, 116
—— Watson’s, 104
Drone fly, 594
Dytiscus marginalis, 607
Echinococcus, 565
Echinodermata, 539
Eggs of insects, 612
Elementary optics, 12
Embedding fluids, list of, 678
—— in paraffin wax, 285
Entomological specimens, mounting, 341
Entozoa, 562
Eosin stain, 315
Eozoon, 492
Epeira diadema, 619
Epidermis of plants, 455
Epithelial cells, 636
Epithelium, mounting, 295
Equisetaceæ, 449
Ergot of rye, 382
Eristalis tenax, 594
Erysiphe Tuckeri, 380
Eudorina, 406
Euglypta, 482
Eurotium repens, 383
Exposure table for photo-micrography, 213
Eye, chromatic aberration of the, 33
—— of cockchafer, 590
—— of fly, 588
—— of whirligig beetle, 608
—— the human, 30
Eye-piece, Abbé’s stereoscopic, 64
—— compensating, 147
Draparnaldia glomerata, 409
Draw-tube, Swift’s, 116
—— Watson’s, 104
Drone fly, 594
Dytiscus marginalis, 607
Echinococcus, 565
Echinodermata, 539
Eggs of insects, 612
Elementary optics, 12
Embedding fluids, list of, 678
—— in paraffin wax, 285
Entomological specimens, mounting, 341
Entozoa, 562
Eosin stain, 315
Eozoon, 492
Epeira diadema, 619
Epidermis of plants, 455
Epithelial cells, 636
Epithelium, mounting, 295
Equisetaceæ, 449
Ergot of rye, 382
Eristalis tenax, 594
Erysiphe Tuckeri, 380
Eudorina, 406
Euglypta, 482
Eurotium repens, 383
Exposure table for photo-micrography, 213
Eye, chromatic aberration of the, 33
—— of cockchafer, 590
—— of fly, 588
—— of whirligig beetle, 608
—— the human, 30
Eye-piece, Abbé’s stereoscopic, 64
—— compensating, 147
Page 816
—— —— Zeiss’s, 147
—— Huyghenian, 139
—— Jackson’s micrometer, 143
—— Ramsden, 142
—— —— micrometer, 145
—— Ross’s, 68
—— Wenham’s double, 63
—— Zeiss’s, 147
Eye-pieces, 139
—— achromatic, 149
—— magnifying powers of, 169
—— projections, 150
—— to clean, 259
Eyes of insects, 584
Favellidium, 415
Feet of insects, observation of, 604
Felices, 446
Fermentation experiments, 361
Fermentations, bacterial, 391
Ferns, 446
—— development of, 446
Fibro-cartilage, 657
Fibrous tissue, 642
—— —— mounting, 296
Filaria sanguinis hominis, 568
Finder, the, 204
—— the Amyot, 205
—— the Maltwood, 204
—— the Okeden, 205
—— Pantacsek’s, 205
Fission formation, 365
Fixing solutions, list of, 678
Flabellum, 528
Flagella, staining of, 336
Flagellate infusoria, 495
—— Huyghenian, 139
—— Jackson’s micrometer, 143
—— Ramsden, 142
—— —— micrometer, 145
—— Ross’s, 68
—— Wenham’s double, 63
—— Zeiss’s, 147
Eye-pieces, 139
—— achromatic, 149
—— magnifying powers of, 169
—— projections, 150
—— to clean, 259
Eyes of insects, 584
Favellidium, 415
Feet of insects, observation of, 604
Felices, 446
Fermentation experiments, 361
Fermentations, bacterial, 391
Ferns, 446
—— development of, 446
Fibro-cartilage, 657
Fibrous tissue, 642
—— —— mounting, 296
Filaria sanguinis hominis, 568
Finder, the, 204
—— the Amyot, 205
—— the Maltwood, 204
—— the Okeden, 205
—— Pantacsek’s, 205
Fission formation, 365
Fixing solutions, list of, 678
Flabellum, 528
Flagella, staining of, 336
Flagellate infusoria, 495
Page 817
Flatness of field, 262
Flax, fibres of, 474
Flea, 629
Florideæ, 413
Flowering plants, 451
Fluke, the, 569
Flustra, 532
Fly, eye of, 588
—— foot of, 602
Focal length of lenses, 22
Focus, method of finding, 271
Foot of fly, 602
Foraminifera, 483
Forceps, 283
—— for mounting, 294
—— stage, 198
Formation and polarisation of crystals, 239
Fossil plants, 475
Fossilised diatomaceæ, 438
Freezing agents, list of, 678
—— microtome, Cathcart’s, 291
—— —— directions for using, 291
Frog-bit, 418
—— plate, 277
Froth-fly, 618
Fungi, industrial uses of, 391
Fungoid diseases, 374
Fungus on plants, 376
—— root, benefit to trees from, 396
—— sewage, 400
—— where found, 379
Gall-fly, 596
Gapeworm, 572
Gelatine, to prepare nutrient, 328
German yeast, 388
Flax, fibres of, 474
Flea, 629
Florideæ, 413
Flowering plants, 451
Fluke, the, 569
Flustra, 532
Fly, eye of, 588
—— foot of, 602
Focal length of lenses, 22
Focus, method of finding, 271
Foot of fly, 602
Foraminifera, 483
Forceps, 283
—— for mounting, 294
—— stage, 198
Formation and polarisation of crystals, 239
Fossil plants, 475
Fossilised diatomaceæ, 438
Freezing agents, list of, 678
—— microtome, Cathcart’s, 291
—— —— directions for using, 291
Frog-bit, 418
—— plate, 277
Froth-fly, 618
Fungi, industrial uses of, 391
Fungoid diseases, 374
Fungus on plants, 376
—— root, benefit to trees from, 396
—— sewage, 400
—— where found, 379
Gall-fly, 596
Gapeworm, 572
Gelatine, to prepare nutrient, 328
German yeast, 388
Page 818
Gillett’s achromatic condenser, 173
Globigerina, 486
Glycerine agar-agar, 330
—— jelly, to make, 297
Gnat, 596
Gnathia, 579
Goniometer, Dr. Leeson’s, 150
Gorgoniidæ, 530
Gosse on noctiluca, 496
Gram’s method of staining bacteria, 335, 338
Grant’s researches on sponges, 507
Gregarinæ, 482, 563
Gromia, 484
Grove’s recommendations for mounting, 299
Gyrinus, eye of, 608
—— leg of, 608
Hæmatoxylin stain, 312
Hairs, structure of, 648
Haliotis splendens, 559
—— tuberculatus, 557
Hansen’s investigations of yeast, 387
Hard structures, mounting, 307
—— woods, cutting sections of, 316
Hardening agents, list of, 677
—— —— absolute alcohol, 287
—— —— chromic acid as, 288
—— —— decalcifying solution as, 288
—— —— methylated spirit as, 288
—— —— Muller’s fluid as, 288
—— —— potassium bichromate, 288
Hardening reagents, 287
—— tissue, 283
Hartea elegans, 535
Heliozoa, 489
Helix absoluta, 558
Globigerina, 486
Glycerine agar-agar, 330
—— jelly, to make, 297
Gnat, 596
Gnathia, 579
Goniometer, Dr. Leeson’s, 150
Gorgoniidæ, 530
Gosse on noctiluca, 496
Gram’s method of staining bacteria, 335, 338
Grant’s researches on sponges, 507
Gregarinæ, 482, 563
Gromia, 484
Grove’s recommendations for mounting, 299
Gyrinus, eye of, 608
—— leg of, 608
Hæmatoxylin stain, 312
Hairs, structure of, 648
Haliotis splendens, 559
—— tuberculatus, 557
Hansen’s investigations of yeast, 387
Hard structures, mounting, 307
—— woods, cutting sections of, 316
Hardening agents, list of, 677
—— —— absolute alcohol, 287
—— —— chromic acid as, 288
—— —— decalcifying solution as, 288
—— —— methylated spirit as, 288
—— —— Muller’s fluid as, 288
—— —— potassium bichromate, 288
Hardening reagents, 287
—— tissue, 283
Hartea elegans, 535
Heliozoa, 489
Helix absoluta, 558
Page 819
—— pomatia, 558
Hepaticæ, 442
Hexactinia, 526
Hirudina medicinalis, 576
Hirudinidæ, 575
His’s method of staining bacteria, 334
Holland’s simple microscope, 75
Holman’s life slide, 277
—— moist chamber, 277
—— syphon slide, 278
Holothurioidea, 543
Honey bee, 598
Horse-tails, 449
House fly, eye of, 588
—— proboscis of, 591
—— tongue of, 592
Human eye, the, 30
—— hair as a test, 269
Huyghenian eye-piece, 139
Hydra, 516
—— fasca, 516
—— stinging, 519
—— viridis, 516
Hydractinia echinata, 523
Hydroid polyps, colony of, 537
Hydrozoa, 515
Ianthinidæ, 550
Iceland spar, 221
Illumination arrangements of the microscope, 673
—— Mercer on, 673
Incubation, apparatus for, 322
—— test for, 263
Incubator, Crookshank’s, 324
Incubators, 324
Indigo plant, 392
Hepaticæ, 442
Hexactinia, 526
Hirudina medicinalis, 576
Hirudinidæ, 575
His’s method of staining bacteria, 334
Holland’s simple microscope, 75
Holman’s life slide, 277
—— moist chamber, 277
—— syphon slide, 278
Holothurioidea, 543
Honey bee, 598
Horse-tails, 449
House fly, eye of, 588
—— proboscis of, 591
—— tongue of, 592
Human eye, the, 30
—— hair as a test, 269
Huyghenian eye-piece, 139
Hydra, 516
—— fasca, 516
—— stinging, 519
—— viridis, 516
Hydractinia echinata, 523
Hydroid polyps, colony of, 537
Hydrozoa, 515
Ianthinidæ, 550
Iceland spar, 221
Illumination arrangements of the microscope, 673
—— Mercer on, 673
Incubation, apparatus for, 322
—— test for, 263
Incubator, Crookshank’s, 324
Incubators, 324
Indigo plant, 392
Page 820
Infusoria, 493
Infusorial life, 349
Injecting, directions for, 304
—— insects, 306
—— lower animals, 305
—— mollusca, 305
—— small animal bodies, 302
—— —— —— —— syringe for, 302
—— with different colours, 304
Injections, to prepare, 303
—— —— subjects for, 303
Injurious insects, 632
Insects, 578, 583
—— antennæ of, 584
—— digestive systems, 586
—— distinctive character of, 583
—— eggs of, 612
—— eyes of, 584
—— injecting, 306
—— injurious, 632
—— mouths of, 584
—— muscles of, 585
—— reproduction of, 587
—— respiratory system of, 607
—— thorax of, 585
—— wings of, 609
Interpretation, errors of, 263
Iris diaphragm, 176
Isthmia enervis, 436
Ixodidæ, 622
Ixodes ricinus, 624
Jackson’s micrometer eye-piece, 143
Jelly-fish, 519, 523
Jungermannia, 442
Infusorial life, 349
Injecting, directions for, 304
—— insects, 306
—— lower animals, 305
—— mollusca, 305
—— small animal bodies, 302
—— —— —— —— syringe for, 302
—— with different colours, 304
Injections, to prepare, 303
—— —— subjects for, 303
Injurious insects, 632
Insects, 578, 583
—— antennæ of, 584
—— digestive systems, 586
—— distinctive character of, 583
—— eggs of, 612
—— eyes of, 584
—— injecting, 306
—— injurious, 632
—— mouths of, 584
—— muscles of, 585
—— reproduction of, 587
—— respiratory system of, 607
—— thorax of, 585
—— wings of, 609
Interpretation, errors of, 263
Iris diaphragm, 176
Isthmia enervis, 436
Ixodidæ, 622
Ixodes ricinus, 624
Jackson’s micrometer eye-piece, 143
Jelly-fish, 519, 523
Jungermannia, 442
Page 821
Koch’s method of staining flagella, 336
Lamp, Baker’s microscope, 191
—— Beck’s complete microscope, 202
—— shells, 539
—— the microscope, 201
—— Watson’s microscope, 203
Lard, embedding in, 285
Larvæ of sea-anemones, 529
Lathe for cutting sections of teeth, 308
Laticiferous tissues, 466
Leaf tissue, 466
Leeson’s goniometer, 150
Leeuwenhoek’s microscope, 4
Leitz’s dissecting microscope, 132
—— microscopes, 132
Lens, bull’s-eye condensing, 199
—— Steinheil’s aplanatic, 77
—— the Coddington, 76
Lenses, concave, 23
—— convex, 18
—— double convex, 19
—— focal length of, 22
—— forms of, 18
—— meniscus form of, 24
—— optical centre of, 20
—— plano-convex, 19
Lepas, 539
Lepisma saccharina, 612
—— scales of, as test, 264
Leptothrix buccalis, 400
Lichenaceæ, 439
Lichens, 439
—— erratic, 441
Lieberkühn’s microscope, 4
Lieberkühn, the, 198
Lamp, Baker’s microscope, 191
—— Beck’s complete microscope, 202
—— shells, 539
—— the microscope, 201
—— Watson’s microscope, 203
Lard, embedding in, 285
Larvæ of sea-anemones, 529
Lathe for cutting sections of teeth, 308
Laticiferous tissues, 466
Leaf tissue, 466
Leeson’s goniometer, 150
Leeuwenhoek’s microscope, 4
Leitz’s dissecting microscope, 132
—— microscopes, 132
Lens, bull’s-eye condensing, 199
—— Steinheil’s aplanatic, 77
—— the Coddington, 76
Lenses, concave, 23
—— convex, 18
—— double convex, 19
—— focal length of, 22
—— forms of, 18
—— meniscus form of, 24
—— optical centre of, 20
—— plano-convex, 19
Lepas, 539
Lepisma saccharina, 612
—— scales of, as test, 264
Leptothrix buccalis, 400
Lichenaceæ, 439
Lichens, 439
—— erratic, 441
Lieberkühn’s microscope, 4
Lieberkühn, the, 198
Page 822
Light, polarisation of, 219
Limax maximus, 558
—— rufus, 558
Limnæan, teeth of, 554
Limnæidæ, 551
Limnæus stagnalis, 551
Lingula pyramidata, 538
Lingulidæ, 538
List of salts, 240
Lister’s correction collar, 155
—— flasks, 322
—— microscope, 81
—— object glass, 154
Live-cages, 274
Live-cells, 277
Live-trough, Botterill’s, 276
Liverworts, 442
Lobosa, 482
Löffler’s method of staining flagella, 336
Logwood, staining by, 293
Lophopus crystallinus, 535
Lyda campestris, 598
Lymph corpuscles, 638
Maddox growing stage, the, 280
Magnifying powers of eye-pieces and objectives, 169
Maltwood finder, the, 204
Maple aphis, 617
Mapping spectra, 253
Marchantia polymorphia, 442
Martin’s microscope, 5
Marzoni’s objective, 152
Mayall’s illuminator, 184
—— mechanical stage, 124
Medusæ, 515, 521
—— a colony of budding, 537
Limax maximus, 558
—— rufus, 558
Limnæan, teeth of, 554
Limnæidæ, 551
Limnæus stagnalis, 551
Lingula pyramidata, 538
Lingulidæ, 538
List of salts, 240
Lister’s correction collar, 155
—— flasks, 322
—— microscope, 81
—— object glass, 154
Live-cages, 274
Live-cells, 277
Live-trough, Botterill’s, 276
Liverworts, 442
Lobosa, 482
Löffler’s method of staining flagella, 336
Logwood, staining by, 293
Lophopus crystallinus, 535
Lyda campestris, 598
Lymph corpuscles, 638
Maddox growing stage, the, 280
Magnifying powers of eye-pieces and objectives, 169
Maltwood finder, the, 204
Maple aphis, 617
Mapping spectra, 253
Marchantia polymorphia, 442
Martin’s microscope, 5
Marzoni’s objective, 152
Mayall’s illuminator, 184
—— mechanical stage, 124
Medusæ, 515, 521
—— a colony of budding, 537
Page 823
Melicerta ringens, 505
Melolontha vulgans, eye of, 590
Meniscus form of lens, 24
Mercer on illumination, 673
Mesoglæa, 525
Mesoglia vermicularis, 410
Methylated spirit as hardening reagent, 288
Metric system of weights and measures, 687
Micrometer, Ramsden’s, 145, 206
—— the stage, 206
Micrometers, 205
Micro-organisms, 373
—— cultivation of, 327
Micro-photography, 210, 674
—— Baker’s apparatus for, 217
—— exposure table, 213
—— Pringle’s apparatus, 217
—— rules for, 214
—— Stringer-Watson’s apparatus for, 674
—— Swift’s apparatus for, 213
Microscope, accessories of the, 197
—— Baker’s advanced student’s, 123
—— —— histological, 125
—— —— Nelson model, 120
—— Beck’s binocular dissecting, 101
—— —— —— National, 99
—— —— large Continental model, 98
—— —— pathological, 95
—— —— Star, 101
—— binocular, Pillischer’s, 128
—— —— Wenham’s, 65
—— Carpenter on binocular, 69
—— compound, 78
—— early history of, 1
—— Holland’s simple, 75
—— Hooke’s water, 2
—— illumination arrangements of the, 673
Melolontha vulgans, eye of, 590
Meniscus form of lens, 24
Mercer on illumination, 673
Mesoglæa, 525
Mesoglia vermicularis, 410
Methylated spirit as hardening reagent, 288
Metric system of weights and measures, 687
Micrometer, Ramsden’s, 145, 206
—— the stage, 206
Micrometers, 205
Micro-organisms, 373
—— cultivation of, 327
Micro-photography, 210, 674
—— Baker’s apparatus for, 217
—— exposure table, 213
—— Pringle’s apparatus, 217
—— rules for, 214
—— Stringer-Watson’s apparatus for, 674
—— Swift’s apparatus for, 213
Microscope, accessories of the, 197
—— Baker’s advanced student’s, 123
—— —— histological, 125
—— —— Nelson model, 120
—— Beck’s binocular dissecting, 101
—— —— —— National, 99
—— —— large Continental model, 98
—— —— pathological, 95
—— —— Star, 101
—— binocular, Pillischer’s, 128
—— —— Wenham’s, 65
—— Carpenter on binocular, 69
—— compound, 78
—— early history of, 1
—— Holland’s simple, 75
—— Hooke’s water, 2
—— illumination arrangements of the, 673
Page 824
—— invention of, 2
—— lamp, the, 201
—— —— Baker’s, 191
—— —— Beck’s, 202
—— —— Watson’s, 203
—— Leitz’s dissecting, 132
—— Leeuwenhoek’s, 4
—— Lieberkühn’s, 4
—— Lister’s, 81
—— manipulation and mode of using the, 258
—— Martin’s, 5
—— Nachet’s, 133
—— —— binocular, 62
—— Pillischer’s binocular, 128
—— —— International, 126
—— Pillischer’s “Kosmos,” 128
—— Powell & Lealand’s, 85
—— —— student’s, 88
—— Pritchard’s diamond, 9
—— Riddell’s binocular, 62
—— Ross’s “Eclipse,” 89
—— —— New Industrial, 90
—— Ross-Jackson, 82
—— Ross-Jackson-Zentmayer, 83
—— Ross-Zentmayer, 91
—— Rousselet’s tank, 126
—— simple, 30, 72, 77
—— simple pocket, 73
—— Sir David Brewster’s, 11
—— Stephenson’s erecting binocular, 71
—— Swift’s advanced student’s, 118
—— —— bacteriological, 116
—— —— four-legged, 114
—— —— histological student’s, 116
—— the bacteriological, 135
—— Watson’s bacteriological, 108
—— —— Edinburgh student’s, 102
—— lamp, the, 201
—— —— Baker’s, 191
—— —— Beck’s, 202
—— —— Watson’s, 203
—— Leitz’s dissecting, 132
—— Leeuwenhoek’s, 4
—— Lieberkühn’s, 4
—— Lister’s, 81
—— manipulation and mode of using the, 258
—— Martin’s, 5
—— Nachet’s, 133
—— —— binocular, 62
—— Pillischer’s binocular, 128
—— —— International, 126
—— Pillischer’s “Kosmos,” 128
—— Powell & Lealand’s, 85
—— —— student’s, 88
—— Pritchard’s diamond, 9
—— Riddell’s binocular, 62
—— Ross’s “Eclipse,” 89
—— —— New Industrial, 90
—— Ross-Jackson, 82
—— Ross-Jackson-Zentmayer, 83
—— Ross-Zentmayer, 91
—— Rousselet’s tank, 126
—— simple, 30, 72, 77
—— simple pocket, 73
—— Sir David Brewster’s, 11
—— Stephenson’s erecting binocular, 71
—— Swift’s advanced student’s, 118
—— —— bacteriological, 116
—— —— four-legged, 114
—— —— histological student’s, 116
—— the bacteriological, 135
—— Watson’s bacteriological, 108
—— —— Edinburgh student’s, 102
Page 825
—— —— histological, 107
—— —— petrological, 111
—— —— portable, 110
—— —— Van Heurck’s, 108
—— Wenham’s binocular, 65
—— —— radial, 90
—— Wollaston’s simple, 74
—— Zeiss’s, 130
Microscopes, Baker’s, 120
—— Beck’s, 95
—— Continental, 130
—— Leitz’s, 132
—— Pillischer’s, 126
—— Ross’s, 88
—— Swift’s, 113
—— Watson’s, 102
Microscopic forms of life, 353
—— vision, principles of, 45
—— —— theory of, 37
Micro-spectroscope, the, 243
Micro-spectroscopic eye-piece, the Sorby-Browning, 247
—— method of using, 250
—— the Browning-Huggins, 245
Microtome, Cambridge rocking, 290
—— Cathcart’s freezing, 291
—— Cole’s section-cutting, 289
—— method of using, 289
Milk, bacteria in, 393
Millipedes, 578
Mineral and geological kingdoms, 670
Mirror, manipulation of, 260
—— the, 195
Mite, cheese, 625
Mites and ticks, 622
Moist stage, 280
Molecular rotation, 238
Mollusca, 545
—— —— petrological, 111
—— —— portable, 110
—— —— Van Heurck’s, 108
—— Wenham’s binocular, 65
—— —— radial, 90
—— Wollaston’s simple, 74
—— Zeiss’s, 130
Microscopes, Baker’s, 120
—— Beck’s, 95
—— Continental, 130
—— Leitz’s, 132
—— Pillischer’s, 126
—— Ross’s, 88
—— Swift’s, 113
—— Watson’s, 102
Microscopic forms of life, 353
—— vision, principles of, 45
—— —— theory of, 37
Micro-spectroscope, the, 243
Micro-spectroscopic eye-piece, the Sorby-Browning, 247
—— method of using, 250
—— the Browning-Huggins, 245
Microtome, Cambridge rocking, 290
—— Cathcart’s freezing, 291
—— Cole’s section-cutting, 289
—— method of using, 289
Milk, bacteria in, 393
Millipedes, 578
Mineral and geological kingdoms, 670
Mirror, manipulation of, 260
—— the, 195
Mite, cheese, 625
Mites and ticks, 622
Moist stage, 280
Molecular rotation, 238
Mollusca, 545
Page 826
—— injecting, 305
—— shell of, 558
Monads in rat’s blood, 372
Monoxenia, 523
Moss-animals, 531
Mosses, 443
Moulds, 380, 381
Mounting apparatus, 352
—— cells for, 340
—— chara, 347
—— entomological specimens, 341
—— epithelium, 295
—— fibrous tissue, 296
—— forceps, 294
—— hard structures, 307
—— media, list of, 678
—— nerve tissue, 296
—— non-striated muscle, 296
—— objects, materials required, 339
—— rock sections, 309
—— spring clip for, 296, 342
—— teeth sections, 308
—— vegetable tissues, 310
Mouse, hair of, 650
Mouth, leptothrix, 400
Mouths of insects, 584
Müller’s fluid, a hardening reagent, 288
Musca domestica, 588
Musci, 443
Muscidæ, 588
Muscles of insects, 585
Muscular fibre, 644
—— —— mounting, 296
Mycetoma, 378
Mycetozoa, 482
Mycorhiza, 396
—— shell of, 558
Monads in rat’s blood, 372
Monoxenia, 523
Moss-animals, 531
Mosses, 443
Moulds, 380, 381
Mounting apparatus, 352
—— cells for, 340
—— chara, 347
—— entomological specimens, 341
—— epithelium, 295
—— fibrous tissue, 296
—— forceps, 294
—— hard structures, 307
—— media, list of, 678
—— nerve tissue, 296
—— non-striated muscle, 296
—— objects, materials required, 339
—— rock sections, 309
—— spring clip for, 296, 342
—— teeth sections, 308
—— vegetable tissues, 310
Mouse, hair of, 650
Mouth, leptothrix, 400
Mouths of insects, 584
Müller’s fluid, a hardening reagent, 288
Musca domestica, 588
Musci, 443
Muscidæ, 588
Muscles of insects, 585
Muscular fibre, 644
—— —— mounting, 296
Mycetoma, 378
Mycetozoa, 482
Mycorhiza, 396
Page 827
Nachet’s binocular microscope, 62
Nails, structure of, 648
Navicula, 427
Neckera antiphyretica, 445
Needles for teasing out sections, 286
Nematoid worms, 556
Nerve tissue, mounting, 296
Nicol prism, 220
Nitella, 418
Nitrate of silver as stain, 297, 298
Noctiluca, 496
Non-striated muscle, mounting, 296
Nose-pieces, 203
Nuclear stains, 311
—— —— carmine, 312
—— —— hæmatoxylin, 312
Nudibranchiata, 547
Nutrient agar-agar, to prepare, 330
—— gelatine, to prepare, 328
—— jelly, to inoculate with bacteria, 331
Object glass, Lister’s, 154
—— to clean, 260
Objective, achromatic, 152
—— changers, 203
—— Powell & Lealand’s oil immersion, 166
Objectives, Baker’s, 168
—— Beck’s, 167
—— English and German, 159
—— high power, 171
—— magnifying powers of, 169
—— Pillischer’s, 169
—— Ross’s, 166
—— Swift’s, 168
—— Watson’s, 167
Objects, collection of, 349
Nails, structure of, 648
Navicula, 427
Neckera antiphyretica, 445
Needles for teasing out sections, 286
Nematoid worms, 556
Nerve tissue, mounting, 296
Nicol prism, 220
Nitella, 418
Nitrate of silver as stain, 297, 298
Noctiluca, 496
Non-striated muscle, mounting, 296
Nose-pieces, 203
Nuclear stains, 311
—— —— carmine, 312
—— —— hæmatoxylin, 312
Nudibranchiata, 547
Nutrient agar-agar, to prepare, 330
—— gelatine, to prepare, 328
—— jelly, to inoculate with bacteria, 331
Object glass, Lister’s, 154
—— to clean, 260
Objective, achromatic, 152
—— changers, 203
—— Powell & Lealand’s oil immersion, 166
Objectives, Baker’s, 168
—— Beck’s, 167
—— English and German, 159
—— high power, 171
—— magnifying powers of, 169
—— Pillischer’s, 169
—— Ross’s, 166
—— Swift’s, 168
—— Watson’s, 167
Objects, collection of, 349
Page 828
Oblique illumination, 186
Oidium albicans, 384
Okeden finder, the, 205
Onion, raphides of, 472
Opisthobranchiata, 548
Optical centre of lenses, 20
Optics, elementary, 12
Oscillariaceæ, 407
Osmic acid as stain, 298
Palates of gastrapods, 556
Palmellaceæ, 407
Palmoglæa macrococca, 401
Pandorina morum, 406
Parabolic reflector, 188
Paraffin wax, embedding in, 285
Parasites, cereal, 381
—— sponge, 512
—— vine, 380
Parasitic diseases of plants, 372
—— fungi of men and animals, 383
Parasitism, De Bary’s investigations in, 395
Patella radiata, 556
Pearls, structure of, 559
Pectinibranchs, 550
Pediastreæ, 422
Pedicellanæ, 543
Peltogaster curvatus, 539
Penetration in objective, 261
Pennatulidæ, 530
Pentacrinoids, 540
Pepperworts, 451
Peronospora viticola, 381
Petiole, 466
Phanerogamiæ, 451
Phanerogams, structure of, 453
Oidium albicans, 384
Okeden finder, the, 205
Onion, raphides of, 472
Opisthobranchiata, 548
Optical centre of lenses, 20
Optics, elementary, 12
Oscillariaceæ, 407
Osmic acid as stain, 298
Palates of gastrapods, 556
Palmellaceæ, 407
Palmoglæa macrococca, 401
Pandorina morum, 406
Parabolic reflector, 188
Paraffin wax, embedding in, 285
Parasites, cereal, 381
—— sponge, 512
—— vine, 380
Parasitic diseases of plants, 372
—— fungi of men and animals, 383
Parasitism, De Bary’s investigations in, 395
Patella radiata, 556
Pearls, structure of, 559
Pectinibranchs, 550
Pediastreæ, 422
Pedicellanæ, 543
Peltogaster curvatus, 539
Penetration in objective, 261
Pennatulidæ, 530
Pentacrinoids, 540
Pepperworts, 451
Peronospora viticola, 381
Petiole, 466
Phanerogamiæ, 451
Phanerogams, structure of, 453
Page 829
Phloem of plants, 454
Pholadidæ, 545
Phomauvicola, 381
Photo-micrography, 210
—— apparatus for, 213
—— Baker’s apparatus for, 217
—— exposure table, 213
—— rules for, 214
—— Swift’s apparatus for, 213
Phylactolæmata, 533
Phylloxera vastatrix, 381
Physalia, 521
Physidæ, 551
Picro-carmine as stain, 299
Pigment cells, 446
Pillischer’s binocular microscope, 128
—— International microscope, 126
—— “Kosmos” microscope, 128
—— objectives, 169
Pinna ingens, 559
Pinnulariæ, 434
Pipette, 319
—— Pasteur’s bulb, 322
Plague, bacillus of, 370
—— the Bombay, 371
Planariæ, 575
Plano-convex lens, 19
Plants, epidermis of, 455
—— fibro-vascular system of, 460
—— flowering, 451
—— fossil, 475
—— ground tissue, system of, 458
—— hairs, 457, 473
—— parasitic diseases of, 374
—— raphides in, 472
—— reproductive organs of, 467
—— spores of parasitic fungus on, 376
Pholadidæ, 545
Phomauvicola, 381
Photo-micrography, 210
—— apparatus for, 213
—— Baker’s apparatus for, 217
—— exposure table, 213
—— rules for, 214
—— Swift’s apparatus for, 213
Phylactolæmata, 533
Phylloxera vastatrix, 381
Physalia, 521
Physidæ, 551
Picro-carmine as stain, 299
Pigment cells, 446
Pillischer’s binocular microscope, 128
—— International microscope, 126
—— “Kosmos” microscope, 128
—— objectives, 169
Pinna ingens, 559
Pinnulariæ, 434
Pipette, 319
—— Pasteur’s bulb, 322
Plague, bacillus of, 370
—— the Bombay, 371
Planariæ, 575
Plano-convex lens, 19
Plants, epidermis of, 455
—— fibro-vascular system of, 460
—— flowering, 451
—— fossil, 475
—— ground tissue, system of, 458
—— hairs, 457, 473
—— parasitic diseases of, 374
—— raphides in, 472
—— reproductive organs of, 467
—— spores of parasitic fungus on, 376
Page 830
—— structure of, 453
—— tissue systems of, 454
—— vascular system of, 464
Plasmodia, 482
Pleurobranchus aurantiacus, 548
—— plumula, 557
Pleurosigma angulatum, 429
—— as a test, 267
—— attenuatum, 429
Plumularia, 521
Pocket lens, Browning’s, 76
—— Coddington’s, 76
Podura-scale test, 268
—— villosa, 611
Polarisation apparatus, 223
—— of light, 219
—— prism, 220
—— —— method of employing, 224
—— rotation of plane of, 231
Polarised crystal of quinidine, 235
Polarising apparatus, Watson’s, 224
Pollen grains, 467
—— —— method of mounting, 467
Polycystina, 489
Polymorphina, 486
Polypomedusæ, 519
Polytrichum undulatum, 445
Polyzoa collecting, 350
Pond-snails, 551
Porifera, 506
Portable microscope, Watson’s, 110
Potassium bichromate as hardening reagent, 288
—— nitrate, crystal of, 232
Powell & Lealand’s microscope, 85
—— oil immersion objective, 166
—— student’s microscope, 88
—— formula for objective, 166
—— tissue systems of, 454
—— vascular system of, 464
Plasmodia, 482
Pleurobranchus aurantiacus, 548
—— plumula, 557
Pleurosigma angulatum, 429
—— as a test, 267
—— attenuatum, 429
Plumularia, 521
Pocket lens, Browning’s, 76
—— Coddington’s, 76
Podura-scale test, 268
—— villosa, 611
Polarisation apparatus, 223
—— of light, 219
—— prism, 220
—— —— method of employing, 224
—— rotation of plane of, 231
Polarised crystal of quinidine, 235
Polarising apparatus, Watson’s, 224
Pollen grains, 467
—— —— method of mounting, 467
Polycystina, 489
Polymorphina, 486
Polypomedusæ, 519
Polytrichum undulatum, 445
Polyzoa collecting, 350
Pond-snails, 551
Porifera, 506
Portable microscope, Watson’s, 110
Potassium bichromate as hardening reagent, 288
—— nitrate, crystal of, 232
Powell & Lealand’s microscope, 85
—— oil immersion objective, 166
—— student’s microscope, 88
—— formula for objective, 166
Page 831
Preparing tissue, 283
Primordial cell, 357
Principal focus, 18
Pringle’s micro-photography apparatus, 217
Prism, 15
—— Nicol’s, 220
Pritchard’s diamond microscope, 9
Proboscis of house fly, 591
Proteolepas, 539
Protococcus invalis, 380
—— pluvialis, 401
Protoplasm, 356
—— staining living, 306
Protozoa, 478
Puccinia graminis, 375
Pyrocystis, 496
Quartz, 231
Quekett on Martin’s microscope, 6
Quinidine, crystals of, 235
Radiolaria, 490
Ramsden eye-piece, 142
—— micrometer eye-piece, 145
Raphides in plants, 472
Rayleigh’s theory of formation of optical images, 44
Reflection, 16
Reflector, Sorby’s, 199
Refraction, 13
—— through prism, 15
Reproductive organs of plants, 467
Resolving power, 262
Retiform tissue, 644
Rezner’s mechanical finger, 343
Rhizocarpeæ, 451
Rhizopoda, 482
Primordial cell, 357
Principal focus, 18
Pringle’s micro-photography apparatus, 217
Prism, 15
—— Nicol’s, 220
Pritchard’s diamond microscope, 9
Proboscis of house fly, 591
Proteolepas, 539
Protococcus invalis, 380
—— pluvialis, 401
Protoplasm, 356
—— staining living, 306
Protozoa, 478
Puccinia graminis, 375
Pyrocystis, 496
Quartz, 231
Quekett on Martin’s microscope, 6
Quinidine, crystals of, 235
Radiolaria, 490
Ramsden eye-piece, 142
—— micrometer eye-piece, 145
Raphides in plants, 472
Rayleigh’s theory of formation of optical images, 44
Reflection, 16
Reflector, Sorby’s, 199
Refraction, 13
—— through prism, 15
Reproductive organs of plants, 467
Resolving power, 262
Retiform tissue, 644
Rezner’s mechanical finger, 343
Rhizocarpeæ, 451
Rhizopoda, 482
Page 832
Riddell’s binocular microscope, 62
Rochelle salt, 232
Rock limpet, 556
—— sections, mounting, 309
Ross’s achromatic condenser, 176
—— compressorium, 275
—— Eclipse microscope, 89
—— eye-pieces, 68
—— microscopes, 88
—— object glass, 154
—— objectives, 166
Ross-Hepworth arc lamp, 218
Ross-Jackson microscope, 82
Ross-Jackson-Zentmayer microscope, 83
Ross-Zentmayer microscope, 91
Rotatoria, mounting, 345
Rotifera, 502
Rousselet’s compressorium, 275
—— method of mounting rotatoria, 345
—— tank microscope, 126
Rye, ergot of, 382
Saccharomyces cerevisiæ, 384
—— ellipsoideus, 385
—— mycoderma, 384
Saccharomycetes, industrial uses of, 391
Salts, list of, 240
Saprolegnia ferox, 411
Sarcode, 357
Saw-fly, 598
Scalariidæ, 550
Scales of butterfly’s wings, 610
Scapander ligniarius, 557
Schäfer’s warm-stage, 282
Scyphomedusæ, 523
Sea-anemone, larvæ of, 529
Rochelle salt, 232
Rock limpet, 556
—— sections, mounting, 309
Ross’s achromatic condenser, 176
—— compressorium, 275
—— Eclipse microscope, 89
—— eye-pieces, 68
—— microscopes, 88
—— object glass, 154
—— objectives, 166
Ross-Hepworth arc lamp, 218
Ross-Jackson microscope, 82
Ross-Jackson-Zentmayer microscope, 83
Ross-Zentmayer microscope, 91
Rotatoria, mounting, 345
Rotifera, 502
Rousselet’s compressorium, 275
—— method of mounting rotatoria, 345
—— tank microscope, 126
Rye, ergot of, 382
Saccharomyces cerevisiæ, 384
—— ellipsoideus, 385
—— mycoderma, 384
Saccharomycetes, industrial uses of, 391
Salts, list of, 240
Saprolegnia ferox, 411
Sarcode, 357
Saw-fly, 598
Scalariidæ, 550
Scales of butterfly’s wings, 610
Scapander ligniarius, 557
Schäfer’s warm-stage, 282
Scyphomedusæ, 523
Sea-anemone, larvæ of, 529
Page 833
Sea-anemones, 526
Sea-cucumber, 540, 543
Sea-hares, 549
Sea-mats, 532
Sea-urchin, 540
Sea-weeds, 409
Section cutting, 283
—— —— Cole’s directions for, 285
Section-cutting microtome, Cole’s, 289
—— lifters, 319
—— scissors, 283
Sections of hard wood, cutting, 316
Selenite, 225
Sepia officinalis, 556
Sertularia, 521
Shadbolt’s turn-table, 295
Sheep-tick, 624
Shell, structure of, 558
—— formation in limnæa, 552
Sieve-tubes, 465
Silk filaments, 474
Silk-worm, 605
Silk-worms, disease of, 363
Silver-side reflector, 198
Simple microscopes, 30, 72, 77
Siphonophora, 521
Sirax gigas, 597
Skin, 646
Smith & Beck’s achromatic condenser, 173
Snow crystals, 237
Sorby-Browning micro-spectroscopic eye-piece, 247
Sorby’s reflector, 199
Spectroscope, cells for use with, 251
—— the, 244
Spectrum of chromule, 255
Sphæroplea annulina, 409
Sphærosira volvex, 406
Sea-cucumber, 540, 543
Sea-hares, 549
Sea-mats, 532
Sea-urchin, 540
Sea-weeds, 409
Section cutting, 283
—— —— Cole’s directions for, 285
Section-cutting microtome, Cole’s, 289
—— lifters, 319
—— scissors, 283
Sections of hard wood, cutting, 316
Selenite, 225
Sepia officinalis, 556
Sertularia, 521
Shadbolt’s turn-table, 295
Sheep-tick, 624
Shell, structure of, 558
—— formation in limnæa, 552
Sieve-tubes, 465
Silk filaments, 474
Silk-worm, 605
Silk-worms, disease of, 363
Silver-side reflector, 198
Simple microscopes, 30, 72, 77
Siphonophora, 521
Sirax gigas, 597
Skin, 646
Smith & Beck’s achromatic condenser, 173
Snow crystals, 237
Sorby-Browning micro-spectroscopic eye-piece, 247
Sorby’s reflector, 199
Spectroscope, cells for use with, 251
—— the, 244
Spectrum of chromule, 255
Sphæroplea annulina, 409
Sphærosira volvex, 406
Page 834
Sphagnaceæ, 446
Spherical aberration, 23
Spiders, 619
Spirilla, 368
Spiro-bacteria, 368
Splenic fever bacillus, 369
Sponges, 506
—— boring, 513
—— Geodia Barretti, 510
—— Grant’s researches on, 507
—— hyalonema, 512
—— parasite on, 512
—— reproduction of, 510
Spongia coalita, 507
Spongiadæ, 506
Spore of parasitic fungus on plants, 576
Spores, 366
Spores, aerobic, 399
—— endogenous, 366
—— staining of, 336
Spring clip for mounting, 296, 342
Stage, Bartley’s warm, 281
—— forceps, 198
—— Maddox growing, 280
—— Mayall’s mechanical, 124
—— moist and warm, 280
—— Schäfer’s, 282
—— Stricker’s, 282
—— Watson’s semi-mechanical, 107
Stain, eosin, 315
Staining animal structures, 292
—— bacteria, 334, 338
—— by logwood, 293
—— cellulose, 314
—— double, 293
—— double and treble, 300
—— living protoplasm, 306
Spherical aberration, 23
Spiders, 619
Spirilla, 368
Spiro-bacteria, 368
Splenic fever bacillus, 369
Sponges, 506
—— boring, 513
—— Geodia Barretti, 510
—— Grant’s researches on, 507
—— hyalonema, 512
—— parasite on, 512
—— reproduction of, 510
Spongia coalita, 507
Spongiadæ, 506
Spore of parasitic fungus on plants, 576
Spores, 366
Spores, aerobic, 399
—— endogenous, 366
—— staining of, 336
Spring clip for mounting, 296, 342
Stage, Bartley’s warm, 281
—— forceps, 198
—— Maddox growing, 280
—— Mayall’s mechanical, 124
—— moist and warm, 280
—— Schäfer’s, 282
—— Stricker’s, 282
—— Watson’s semi-mechanical, 107
Stain, eosin, 315
Staining animal structures, 292
—— bacteria, 334, 338
—— by logwood, 293
—— cellulose, 314
—— double, 293
—— double and treble, 300
—— living protoplasm, 306
Page 835
—— of flagella, 336
—— of spores, 336
—— tissue, 283
Stains and staining methods, list of, 679
Stains, chloride of gold, 297
—— chloride of palladium, 298
—— contrast, 313
—— double and treble, 300
—— nitrate of silver, 297, 298
—— osmic acid, 298
—— picro-carmine, 299
—— single, 298
Starch, 238
—— granules, 469
—— —— of arrowroot, 470
—— —— of potato, 470
—— —— of wheat, 470
Star-fish, 540
Steinheil’s aplanatic lens, 77
Stentors, 501
Stephanoceros, 504
Stephanosphæra pluvialis, 403
Stephenson’s erecting binocular microscope, 71
Stereoscope, the, 60
Stereoscopic binocular vision, 60
Sterilised instruments, 321
Sterilisers, 324
—— Hearson’s, 325
—— steam, 325
—— —— Dr. Koch’s, 325
Sting of bee, 596
—— of wasp, 596
Stock-bottle, 279
Stomata of iris, 456
—— water pores, 457
Stone-lilies, 542
Stonewort, 415
—— of spores, 336
—— tissue, 283
Stains and staining methods, list of, 679
Stains, chloride of gold, 297
—— chloride of palladium, 298
—— contrast, 313
—— double and treble, 300
—— nitrate of silver, 297, 298
—— osmic acid, 298
—— picro-carmine, 299
—— single, 298
Starch, 238
—— granules, 469
—— —— of arrowroot, 470
—— —— of potato, 470
—— —— of wheat, 470
Star-fish, 540
Steinheil’s aplanatic lens, 77
Stentors, 501
Stephanoceros, 504
Stephanosphæra pluvialis, 403
Stephenson’s erecting binocular microscope, 71
Stereoscope, the, 60
Stereoscopic binocular vision, 60
Sterilised instruments, 321
Sterilisers, 324
—— Hearson’s, 325
—— steam, 325
—— —— Dr. Koch’s, 325
Sting of bee, 596
—— of wasp, 596
Stock-bottle, 279
Stomata of iris, 456
—— water pores, 457
Stone-lilies, 542
Stonewort, 415
Page 836
Stricker’s warm stage, 282
Stringer’s apparatus for micro-photography, 674
Stylonychia mytilus, 500
Stylopidæ, 628
Substage condenser, 193
Subterranean fungi, 397
Sun-animalcules, 489
Swift’s advanced student’s microscope, 118
—— bacteriological microscope, 116
—— draw-tube, 116
—— four-legged microscope, 114
—— histological student’s microscope, 116
—— horizontal camera, 213
—— illuminating apparatus, 183
—— microscopes, 113
— objectives, 168
Tables, aperture, 58
Tænia, 564
Tanning skins, 393
Tardigrada, 631
Teasing out sections, needles for, 286
—— —— —— under condensed light, 287
Teeth, 652
—— lathe for cutting sections of, 308
—— method of cutting sections of, 308
—— mounting, 308
Tenent-hairs, 603
Terebella littoralis, 577
Terebratulata rubicuna, 559
Testacella maugei, 556
Test for illumination, 263
Test object, blood as a, 263
Test object, human hair as, 269
—— —— lepisma as, 264
—— —— pleurosigma, 267
Stringer’s apparatus for micro-photography, 674
Stylonychia mytilus, 500
Stylopidæ, 628
Substage condenser, 193
Subterranean fungi, 397
Sun-animalcules, 489
Swift’s advanced student’s microscope, 118
—— bacteriological microscope, 116
—— draw-tube, 116
—— four-legged microscope, 114
—— histological student’s microscope, 116
—— horizontal camera, 213
—— illuminating apparatus, 183
—— microscopes, 113
— objectives, 168
Tables, aperture, 58
Tænia, 564
Tanning skins, 393
Tardigrada, 631
Teasing out sections, needles for, 286
—— —— —— under condensed light, 287
Teeth, 652
—— lathe for cutting sections of, 308
—— method of cutting sections of, 308
—— mounting, 308
Tenent-hairs, 603
Terebella littoralis, 577
Terebratulata rubicuna, 559
Testacella maugei, 556
Test for illumination, 263
Test object, blood as a, 263
Test object, human hair as, 269
—— —— lepisma as, 264
—— —— pleurosigma, 267
Page 837
—— —— podura-scale, 268
Test-plate, Abbé’s, 164
Threadworm, 566
Thorax of insects, 585
Thuricola valvata, 500
Tick, dog, 624
—— sheep, 624
Ticks, 622
Tissue, adipose, 644
—— bacteria in sections of, 337
—— fibrous, 642
—— hardening, 283
—— preparing, 283
—— retiform, 644
—— staining, 283
—— systems of plants, 454
Tongue of butterfly, 605
—— of house fly, 592
—— of wasp, 595
Tooth substance, 654
Topaz, 231
Tourmaline, 225
Trematode worms, 569
Trichina spiralis, 567
Trichomes of plants, 457
Troughs, 274
Truffle, 397
Tuber cibarium, 397
Tubicola, 576
Tubipora, 530
Tubularia dumortierii, 537
Tunicata, 549
Turbo marmoratus, 557
Turn-table, Shadbolt’s, 295
Typhoid bacillus, 370
Test-plate, Abbé’s, 164
Threadworm, 566
Thorax of insects, 585
Thuricola valvata, 500
Tick, dog, 624
—— sheep, 624
Ticks, 622
Tissue, adipose, 644
—— bacteria in sections of, 337
—— fibrous, 642
—— hardening, 283
—— preparing, 283
—— retiform, 644
—— staining, 283
—— systems of plants, 454
Tongue of butterfly, 605
—— of house fly, 592
—— of wasp, 595
Tooth substance, 654
Topaz, 231
Tourmaline, 225
Trematode worms, 569
Trichina spiralis, 567
Trichomes of plants, 457
Troughs, 274
Truffle, 397
Tuber cibarium, 397
Tubicola, 576
Tubipora, 530
Tubularia dumortierii, 537
Tunicata, 549
Turbo marmoratus, 557
Turn-table, Shadbolt’s, 295
Typhoid bacillus, 370
Page 838
Ulvaceæ, the, 411
Ulva lactuca, 411
—— thermalis, 411
Urinary salts, 236
Vallisneria, 418
Varley’s live-box, 274
Varnishes, 339
Vascular system of plants, 464
Vaucheria, 410
Vegetable tissues, staining and mounting, 310
Veins, 662
Velutina lævigata, 557
Vertebrata, 633
Vine parasites, 380
Violet sea-snail, 550
Visual angle, 72
—— judgment, 37
Volvocineæ, 404
Vorticellidæ, 499
Walmsley’s turn-table, 340
Warm chamber, Pfeiffer’s, 323
—— stage, 280
—— —— Bartley’s, 281
—— —— Schäfer’s, 282
—— —— Stricker’s, 282
Wasp, sting of, 596
—— tongue of, 595
Water thyme, 419
Watson’s achromatic condenser, 177
—— bacteriological Van Heurck’s microscope, 108
—— Edinburgh student’s microscope, 102
—— histological microscope, 107
—— mechanical draw-tube, 104
—— microscope lamp, 203
Ulva lactuca, 411
—— thermalis, 411
Urinary salts, 236
Vallisneria, 418
Varley’s live-box, 274
Varnishes, 339
Vascular system of plants, 464
Vaucheria, 410
Vegetable tissues, staining and mounting, 310
Veins, 662
Velutina lævigata, 557
Vertebrata, 633
Vine parasites, 380
Violet sea-snail, 550
Visual angle, 72
—— judgment, 37
Volvocineæ, 404
Vorticellidæ, 499
Walmsley’s turn-table, 340
Warm chamber, Pfeiffer’s, 323
—— stage, 280
—— —— Bartley’s, 281
—— —— Schäfer’s, 282
—— —— Stricker’s, 282
Wasp, sting of, 596
—— tongue of, 595
Water thyme, 419
Watson’s achromatic condenser, 177
—— bacteriological Van Heurck’s microscope, 108
—— Edinburgh student’s microscope, 102
—— histological microscope, 107
—— mechanical draw-tube, 104
—— microscope lamp, 203
Page 839
—— microscopes, 102
—— parachromatic condenser, 182
—— petrological microscope, 111
—— portable microscope, 110
—— semi-mechanical stage, 107
Webster-Collins condenser, 186
Weights and measures, metric system of, 687
Wenham’s binocular microscope, 65
—— double eye-piece, 189
—— immersion condenser, 189
—— parabolic condenser, 186
—— —— reflector, 187
—— radial microscope, 90
Wheat rust, 374
—— starch, 470
Wheel animalcules, 502
Whirligig-beetle, eyes of, 608
—— —— leg of, 608
Wings of butterfly, 610
—— of insects, 609
—— of moth, 610
Winogradsky’s investigations of bacteria, 398
Wollaston’s simple microscope, 74
Wood, formation of, 462
Wool, 474
Worms, 562
Wort-gelatine, 330
Xylem of plants, 462
Yeast cells, 384
—— German, 388
—— Hansen’s investigations of, 387
Zeiss’s compensating eye-piece, 147
—— parachromatic condenser, 182
—— petrological microscope, 111
—— portable microscope, 110
—— semi-mechanical stage, 107
Webster-Collins condenser, 186
Weights and measures, metric system of, 687
Wenham’s binocular microscope, 65
—— double eye-piece, 189
—— immersion condenser, 189
—— parabolic condenser, 186
—— —— reflector, 187
—— radial microscope, 90
Wheat rust, 374
—— starch, 470
Wheel animalcules, 502
Whirligig-beetle, eyes of, 608
—— —— leg of, 608
Wings of butterfly, 610
—— of insects, 609
—— of moth, 610
Winogradsky’s investigations of bacteria, 398
Wollaston’s simple microscope, 74
Wood, formation of, 462
Wool, 474
Worms, 562
Wort-gelatine, 330
Xylem of plants, 462
Yeast cells, 384
—— German, 388
—— Hansen’s investigations of, 387
Zeiss’s compensating eye-piece, 147
Page 840
—— cover-glass gauge, 165
—— microscope, 130
Zentmayer’s Holman syphon slide, 278
Zoophytes, 515
BRADBURY, AGNEW, & CO. LD., PRINTERS, LONDON AND TONBRIDGE.
—— microscope, 130
Zentmayer’s Holman syphon slide, 278
Zoophytes, 515
BRADBURY, AGNEW, & CO. LD., PRINTERS, LONDON AND TONBRIDGE.
Page 841
FOOTNOTES:
1 My earliest acquaintance with the Microscope occurred in the
thirties, when I fortunately became possessed of a Culpeper-
Scarlet instrument, figured in the title-page.
2 At the time this was written, scarcely a book of the kind had been
published at a price within the reach of the student.
3 For fuller information, see the Cantor Lectures on the
Microscope, by the late John Mayall, F.R.M.S., “Society of Arts
Journal,” 1885.
4 “A Practical Treatise on the Use of the Microscope.” London,
1855.
5 For further information, I must refer my readers to Parkinson’s
“Treatise on Optics;” Herschel’s “Familiar Lectures on Light;”
“Cyclopædia Britannica;” Everett’s translation of Deschanel’s
“Physics;” and Nägeli and Schwendener’s “Theory and Practice
of the Microscope,” translated by Frank Crisp, LL.D.
6 The cornea of the eye is not so entirely the simple transparent
structure as it at first sight may appear to be. It is composed of
several layers, the most important of which is the nerve layer,
consisting of innumerable ganglionic stellate plexus of cells
held together by a network, as seen in Fig. 21, a small section
stained by chloride of gold, and magnified 300 diameters.
Beneath the nucleated nerve cells is a second layer of stellate
cells, varying a little in their form. These nerve and stellate cells
serve the purpose of maintaining the cornea in health, and must
play a significant part in the dioptric system.
1 My earliest acquaintance with the Microscope occurred in the
thirties, when I fortunately became possessed of a Culpeper-
Scarlet instrument, figured in the title-page.
2 At the time this was written, scarcely a book of the kind had been
published at a price within the reach of the student.
3 For fuller information, see the Cantor Lectures on the
Microscope, by the late John Mayall, F.R.M.S., “Society of Arts
Journal,” 1885.
4 “A Practical Treatise on the Use of the Microscope.” London,
1855.
5 For further information, I must refer my readers to Parkinson’s
“Treatise on Optics;” Herschel’s “Familiar Lectures on Light;”
“Cyclopædia Britannica;” Everett’s translation of Deschanel’s
“Physics;” and Nägeli and Schwendener’s “Theory and Practice
of the Microscope,” translated by Frank Crisp, LL.D.
6 The cornea of the eye is not so entirely the simple transparent
structure as it at first sight may appear to be. It is composed of
several layers, the most important of which is the nerve layer,
consisting of innumerable ganglionic stellate plexus of cells
held together by a network, as seen in Fig. 21, a small section
stained by chloride of gold, and magnified 300 diameters.
Beneath the nucleated nerve cells is a second layer of stellate
cells, varying a little in their form. These nerve and stellate cells
serve the purpose of maintaining the cornea in health, and must
play a significant part in the dioptric system.
Page 842
7 The standard condition of perfect vision is termed emmetropia.
8 Landolt; “The Accommodation and Refraction of the Eye,”
1886.
9 µ = ·001 of a millimetre. This measurement is now universally
employed in microscopy.
10 Diffraction effects may be observed without a microscope,
indeed, the more striking are seen in connection with telescopic
vision. A beautiful series of phenomena in illustration of the
diffraction of light may be produced as follows: Draw on a large
sheet of paper a series of geometrical figures, arranged at equal
distances in a circle. A collodion photographic picture of these
being taken, a series of small transparent apertures in the
elsewhere opaque film will result. This film is then mounted, so
that it may be in turn brought before the centre of a small hand
telescope, previously adjusted to view an image of the sun. In
this way we have an apparatus of the most compact form, and
by means of which a series of fifty or more phenomena may be
brought into view in a few minutes. These pictures being very
small (occupying on an average area one-tenth of an inch in
diameter), inaccuracies of surface and substance of the glass
may be neglected. A film of Canada balsam with which the glass
is cemented over the picture produces no disturbance. There is a
manifest advantage in the figures being small, as the size of the
image is in inverse proportion to the size of the aperture.
11 Carpenter, “The Microscope,” p. 65, 1891.
12 “Phil. Mag.,” viii., p. 167 (1896).
13 Professor Stokes wrote me in the following flattering terms:
—“What you have submitted to me on the subject of apertures is
so sound, clear, and succinct, that I have nothing to add to it.
The method adapted as you have explained respecting the
immersion system, I consider to be perfectly satisfactory.”
Subsequently, and at my request, Sir George Stokes contributed
8 Landolt; “The Accommodation and Refraction of the Eye,”
1886.
9 µ = ·001 of a millimetre. This measurement is now universally
employed in microscopy.
10 Diffraction effects may be observed without a microscope,
indeed, the more striking are seen in connection with telescopic
vision. A beautiful series of phenomena in illustration of the
diffraction of light may be produced as follows: Draw on a large
sheet of paper a series of geometrical figures, arranged at equal
distances in a circle. A collodion photographic picture of these
being taken, a series of small transparent apertures in the
elsewhere opaque film will result. This film is then mounted, so
that it may be in turn brought before the centre of a small hand
telescope, previously adjusted to view an image of the sun. In
this way we have an apparatus of the most compact form, and
by means of which a series of fifty or more phenomena may be
brought into view in a few minutes. These pictures being very
small (occupying on an average area one-tenth of an inch in
diameter), inaccuracies of surface and substance of the glass
may be neglected. A film of Canada balsam with which the glass
is cemented over the picture produces no disturbance. There is a
manifest advantage in the figures being small, as the size of the
image is in inverse proportion to the size of the aperture.
11 Carpenter, “The Microscope,” p. 65, 1891.
12 “Phil. Mag.,” viii., p. 167 (1896).
13 Professor Stokes wrote me in the following flattering terms:
—“What you have submitted to me on the subject of apertures is
so sound, clear, and succinct, that I have nothing to add to it.
The method adapted as you have explained respecting the
immersion system, I consider to be perfectly satisfactory.”
Subsequently, and at my request, Sir George Stokes contributed
Page 843
a valuable paper on the subject to the “Transactions of the Royal
Microscopical Society,” 1876, on “The Theoretical Limit of
Aperture.”
14 “On the Estimation of Aperture in the Microscope,” “Journal of
the Royal Microscopical Society,” series ii. vol. i.; “Notes on
Aperture, Microscopic Vision, and the Value of Wide-angled
Immersion Objectives,” 1881.
15 Numerical aperture is generally used in the sense in which it was
introduced in 1873 by Professor Abbe, on the basis of his
theoretical investigations. Numerical aperture represents the
ratio between the radius of the effective aperture (p) of the
system on the side where the image is formed—more accurately
the radius of the emerging pencils measured in the upper focal
plane of the objective—and the equivalent focal length (f) of the
latter, i.e.,
Numerical aperture = p/f.
This ratio is equal to the product of the sine of half the angle of
aperture u of the incident pencils and the refractive index n of
the medium, situated in front of the objective. With dry lenses n
has therefore the value 1; with immersion lenses it is equal to
the refractive index of the particular immersion fluid:
Numerical aperture = n Sin u.
The numerical aperture of a lens determines all its essential
qualities; the brightness of the image increases with a given
magnification and, other things being equal, as the square of the
aperture; the resolving and defining powers are directly related
to it, the focal depth of differentiation of depths varies inversely
as the aperture, and so forth. (Abbe, “The Estimation of
Aperture,” “Journal of the Royal Microscopical Society,” 1881,
p. 389.)
16 “Journal of the Royal Microscopical Society.”
Microscopical Society,” 1876, on “The Theoretical Limit of
Aperture.”
14 “On the Estimation of Aperture in the Microscope,” “Journal of
the Royal Microscopical Society,” series ii. vol. i.; “Notes on
Aperture, Microscopic Vision, and the Value of Wide-angled
Immersion Objectives,” 1881.
15 Numerical aperture is generally used in the sense in which it was
introduced in 1873 by Professor Abbe, on the basis of his
theoretical investigations. Numerical aperture represents the
ratio between the radius of the effective aperture (p) of the
system on the side where the image is formed—more accurately
the radius of the emerging pencils measured in the upper focal
plane of the objective—and the equivalent focal length (f) of the
latter, i.e.,
Numerical aperture = p/f.
This ratio is equal to the product of the sine of half the angle of
aperture u of the incident pencils and the refractive index n of
the medium, situated in front of the objective. With dry lenses n
has therefore the value 1; with immersion lenses it is equal to
the refractive index of the particular immersion fluid:
Numerical aperture = n Sin u.
The numerical aperture of a lens determines all its essential
qualities; the brightness of the image increases with a given
magnification and, other things being equal, as the square of the
aperture; the resolving and defining powers are directly related
to it, the focal depth of differentiation of depths varies inversely
as the aperture, and so forth. (Abbe, “The Estimation of
Aperture,” “Journal of the Royal Microscopical Society,” 1881,
p. 389.)
16 “Journal of the Royal Microscopical Society.”
Page 844
17 “Journal Roy. Micros. Soc.,” p. 19, 1878, and p. 20, 1880.
18 “The Magnifying Power of Short Spaces” has been ably
elucidated by John Gorham, Esq., M.R.C.S. “Journal of
Microscopical Society,” October, 1854.
19 The late Mr. Coddington, of Cambridge, who had a high opinion
of the value of this lens, had one of these grooved spheres
executed by Mr. Carey, who gave it the name of the Coddington
Lens, supposing that it was invented by the person who
employed him, whereas Mr. Coddington never laid claim to it,
and the circumstance of his having one made was not known
until nine years after it was described by Sir David Brewster in
the “Edinburgh Journal.”
20 “Journal of the Royal Microscopical Society, 1890,” p. 420.
21 “Journal of the Royal Microscopical Society, 1880,” p. 1050.
22 Apo-chromatic, from the Greek, signifying freedom from colour.
23 Prof. Abbe “On Stephenson’s System of Homogeneous
Immersion for Microscope Objectives,” “Journal of the Royal
Microscopical Society,” II. (1879), p. 256, and on “The Essence
of Homogeneous Immersion,” Ibid., I. (1881), p. 131.
24 Reichert, in his catalogue, does not clearly indicate what the
initial powers of his eye-pieces are.
25 Messrs. Ross have two series of eye-pieces, both Huyghenian.
One series is for use with the English 10-inch tube-body, and is
distinguished by Roman letters, and the other by numerals, and
made as is usual on the Continent, and for use with the shorter
tube-body 6½-inch. The initial powers given in the table are for
the 10-inch tube, and for the shorter must be read as follows:—
1 2 3 4 }
with 6½-inch tube.
4 6 8 12 }
18 “The Magnifying Power of Short Spaces” has been ably
elucidated by John Gorham, Esq., M.R.C.S. “Journal of
Microscopical Society,” October, 1854.
19 The late Mr. Coddington, of Cambridge, who had a high opinion
of the value of this lens, had one of these grooved spheres
executed by Mr. Carey, who gave it the name of the Coddington
Lens, supposing that it was invented by the person who
employed him, whereas Mr. Coddington never laid claim to it,
and the circumstance of his having one made was not known
until nine years after it was described by Sir David Brewster in
the “Edinburgh Journal.”
20 “Journal of the Royal Microscopical Society, 1890,” p. 420.
21 “Journal of the Royal Microscopical Society, 1880,” p. 1050.
22 Apo-chromatic, from the Greek, signifying freedom from colour.
23 Prof. Abbe “On Stephenson’s System of Homogeneous
Immersion for Microscope Objectives,” “Journal of the Royal
Microscopical Society,” II. (1879), p. 256, and on “The Essence
of Homogeneous Immersion,” Ibid., I. (1881), p. 131.
24 Reichert, in his catalogue, does not clearly indicate what the
initial powers of his eye-pieces are.
25 Messrs. Ross have two series of eye-pieces, both Huyghenian.
One series is for use with the English 10-inch tube-body, and is
distinguished by Roman letters, and the other by numerals, and
made as is usual on the Continent, and for use with the shorter
tube-body 6½-inch. The initial powers given in the table are for
the 10-inch tube, and for the shorter must be read as follows:—
1 2 3 4 }
with 6½-inch tube.
4 6 8 12 }
Page 845
26 This centring-glass consists of a tubular cap with a minute
aperture, containing two plano-convex lenses, so adjusted that
the image of the aperture in the object-glass and the images of
the aperture of the lenses and the diaphragms contained in the
tube which holds the illuminating combination, may be all in
focus at the same time, so that by the same adjustment they may
be brought sufficiently near to recognise their centricity.
27 Summary of the value of parabolic illumination and immersion
illuminators, by the late Mr. J. Mayall, will be found on p. 27,
“Journal of the Royal Microscopical Society” (1879).
28 Messrs. Baker and Swift have constructed lamps with removal
and fixed achromatic bull’s-eye lenses in gymbal, and
changeable tinted glass screens. Either of these will add to the
usefulness of the lamp in bacteriological research work. Baker’s
is constructed on the Herschel doublet formula, and should
therefore be free from aberration. It is mounted on a heavy brass
tripod foot, has vertical and horizontal movements by rack and
pinion, brass reservoir, with screw opening for filling, metal
chimney to take 3 × 1½-inch glass slip, removable frame for
carrying tinted glass screens, &c.
29 “Journal of the Royal Microscopical Society,” p. 365, 1896.
30 Dr. G. A. Piersoll, “American Annual of Photography,” 1890.
31 “Journal of the Royal Microscopical Society,” 1892, p. 684.
32 “Journal of the Royal Microscopical Society,” p. 578, 1897.
33 Herapath’s test-fluid is a mixture of three drachms of pure acetic
acid, one drachm of alcohol, and three drops of sulphuric acid.
34 “Journal of the Royal Microscopic Society,” 1867.
35 Born in 1787, at Straubing, a small town in Bavaria.
aperture, containing two plano-convex lenses, so adjusted that
the image of the aperture in the object-glass and the images of
the aperture of the lenses and the diaphragms contained in the
tube which holds the illuminating combination, may be all in
focus at the same time, so that by the same adjustment they may
be brought sufficiently near to recognise their centricity.
27 Summary of the value of parabolic illumination and immersion
illuminators, by the late Mr. J. Mayall, will be found on p. 27,
“Journal of the Royal Microscopical Society” (1879).
28 Messrs. Baker and Swift have constructed lamps with removal
and fixed achromatic bull’s-eye lenses in gymbal, and
changeable tinted glass screens. Either of these will add to the
usefulness of the lamp in bacteriological research work. Baker’s
is constructed on the Herschel doublet formula, and should
therefore be free from aberration. It is mounted on a heavy brass
tripod foot, has vertical and horizontal movements by rack and
pinion, brass reservoir, with screw opening for filling, metal
chimney to take 3 × 1½-inch glass slip, removable frame for
carrying tinted glass screens, &c.
29 “Journal of the Royal Microscopical Society,” p. 365, 1896.
30 Dr. G. A. Piersoll, “American Annual of Photography,” 1890.
31 “Journal of the Royal Microscopical Society,” 1892, p. 684.
32 “Journal of the Royal Microscopical Society,” p. 578, 1897.
33 Herapath’s test-fluid is a mixture of three drachms of pure acetic
acid, one drachm of alcohol, and three drops of sulphuric acid.
34 “Journal of the Royal Microscopic Society,” 1867.
35 Born in 1787, at Straubing, a small town in Bavaria.
Page 846
36 Dr. Thudicum’s “Tenth Report of the Medical Officer of the
Privy Council, 1867.” Mr. Sorby “On Some Improvements in
the Spectrum Method of Detecting Blood.” “Journal of the
Royal Microscopical Society,” 1871.
37 “On the Reduction and Oxidation of the Colouring-matter of the
Blood” (“Proc. of the Royal Soc.” vol. xiii. p. 355). The
oxidising solution is made as follows:—To a solution of proto-
sulphate of iron, enough tartaric acid is added to prevent
precipitation by alkalies. A small quantity of this solution, made
slightly alkaline by ammonia or carbonate of soda, is to be
added to the weak solution of blood in water.
38 “Journal of the Royal Microscopical Society,” 1869.
39 Professor Sylvanus Thompson, “On the Measurement of
Lenses,” “Journal of the Royal Microscopical Society,” 1892, p.
109.
40 “Journal of the Royal Microscopical Society,” 2nd Series, Vol.
iv., p. 542.
41 Mr. J. F. Smith, “On the Structure of the Valve of Pleurosigma
Pellucida,” “Quekett Club Trans.”
42 “Quarterly Journal of Microscopical Science,” New Series, Vol.
viii., 1878.
43 It is quite possible also for the student to make his own
microscope stand. Mr. Field in the “English Mechanic,” pp. 171
et seq., 1897, furnishes numerous working drawings for the
construction of a high-class stand, together with patterns for the
metal work.
44 “Modern Microscopy,” by Martin J. Cole.
45 With regard to the use of absolute alcohol, this re-agent requires
to be used with caution; all minute details are lost, and it causes
Privy Council, 1867.” Mr. Sorby “On Some Improvements in
the Spectrum Method of Detecting Blood.” “Journal of the
Royal Microscopical Society,” 1871.
37 “On the Reduction and Oxidation of the Colouring-matter of the
Blood” (“Proc. of the Royal Soc.” vol. xiii. p. 355). The
oxidising solution is made as follows:—To a solution of proto-
sulphate of iron, enough tartaric acid is added to prevent
precipitation by alkalies. A small quantity of this solution, made
slightly alkaline by ammonia or carbonate of soda, is to be
added to the weak solution of blood in water.
38 “Journal of the Royal Microscopical Society,” 1869.
39 Professor Sylvanus Thompson, “On the Measurement of
Lenses,” “Journal of the Royal Microscopical Society,” 1892, p.
109.
40 “Journal of the Royal Microscopical Society,” 2nd Series, Vol.
iv., p. 542.
41 Mr. J. F. Smith, “On the Structure of the Valve of Pleurosigma
Pellucida,” “Quekett Club Trans.”
42 “Quarterly Journal of Microscopical Science,” New Series, Vol.
viii., 1878.
43 It is quite possible also for the student to make his own
microscope stand. Mr. Field in the “English Mechanic,” pp. 171
et seq., 1897, furnishes numerous working drawings for the
construction of a high-class stand, together with patterns for the
metal work.
44 “Modern Microscopy,” by Martin J. Cole.
45 With regard to the use of absolute alcohol, this re-agent requires
to be used with caution; all minute details are lost, and it causes
Page 847
irregular shrinking of the finer tissues, while fibrous tissue is
brought into undue prominence at the expense of the cellular
elements. Consequently in certain biological laboratories the
method of hardening in alcohol has been abandoned in favour of
other re-agents.
46 “Journal of Anatomy and Physiology,” XX. 1881, p. 349.
47 “Journal of the Quekett Club,” July, 1893, and March, 1895.
48 Mr. John Hood, 50, Dallfield Walk, Dundee, offers a weekly
supply of infusorial life for a small annual subscription, or a
single tube by post at the trifling cost of one shilling.
49 Professor Marshall Ward, F.R.S., “Address to the Botanical
Section of the British Association, 1897.”
50 “British Medical Journal,” March 26, 1859; “Medical Times and
Gazette” and “Popular Science Review,” 1862.
51 “Parasitic Diseases,” “Journ. of the Royal Micros. Soc. of
Lond.,” 1859-60.
52 There are several other kinds of bacteria infesting milk, some of
which are motile, others non-motile, producing acidity and
colouring matter, as B. prodigiosus, red-milk; B. synxanthus,
yellow milk; B. lactis aerogens, which are pathogenic; B. lactis
albus, which coagulate milk; and another form, which is
productive of slimy or ropy-milk.
53 “Parasitic Diseases of the Skin,” 1859-73, p. 30. Bailliere,
Tindal, and Cox.
54 “Organic Germ Theory of Disease,” “Medical Times and
Gazette,” p. 685, 1870.
55 F. Cohn on the “Natural History of Protococcus pluvialis.”
56 Pritchard’s “Infusoria,” p. 24, Plate I., 4th edition.
brought into undue prominence at the expense of the cellular
elements. Consequently in certain biological laboratories the
method of hardening in alcohol has been abandoned in favour of
other re-agents.
46 “Journal of Anatomy and Physiology,” XX. 1881, p. 349.
47 “Journal of the Quekett Club,” July, 1893, and March, 1895.
48 Mr. John Hood, 50, Dallfield Walk, Dundee, offers a weekly
supply of infusorial life for a small annual subscription, or a
single tube by post at the trifling cost of one shilling.
49 Professor Marshall Ward, F.R.S., “Address to the Botanical
Section of the British Association, 1897.”
50 “British Medical Journal,” March 26, 1859; “Medical Times and
Gazette” and “Popular Science Review,” 1862.
51 “Parasitic Diseases,” “Journ. of the Royal Micros. Soc. of
Lond.,” 1859-60.
52 There are several other kinds of bacteria infesting milk, some of
which are motile, others non-motile, producing acidity and
colouring matter, as B. prodigiosus, red-milk; B. synxanthus,
yellow milk; B. lactis aerogens, which are pathogenic; B. lactis
albus, which coagulate milk; and another form, which is
productive of slimy or ropy-milk.
53 “Parasitic Diseases of the Skin,” 1859-73, p. 30. Bailliere,
Tindal, and Cox.
54 “Organic Germ Theory of Disease,” “Medical Times and
Gazette,” p. 685, 1870.
55 F. Cohn on the “Natural History of Protococcus pluvialis.”
56 Pritchard’s “Infusoria,” p. 24, Plate I., 4th edition.
Page 848
57 In order to detect the presence of starch-grains in plants, the
tissue must be kept in alcohol exposed to light, until the whole
of the chlorophyll is dissolved out; it must then be treated for
several hours in a strong solution of potash. After neutralisation
with acetic acid, the tissue may be treated with iodine, which
colours it blue, or with coralline solution, which colours it pink.
58 Verhandl. d. Natur. Hist. Jahr. xx. p. 1. “Micros. Jour. Science,”
vol. iii., p. 120.
59 For instance, where the yellow Palmella is found the
Chlorococcus will assume a yellow tinge in its soridial stage.
Viewed by transmitted light the sori are seen as opaque balls,
with an irregular outline.
60 “Contributions to the Knowledge of the Development of the
Gonidia of Lichens.” By J. Braxton Hicks, M.D., “Quarterly
Journal of Microscopical Science,” vol. viii., 860, p. 239.
61 Berkeley’s “Introduction to Cryptogamic Botany,” 1857.
62 For more detailed information on the structure and classification
of unicellular plants, and cryptogams, the reader is referred to
Ralfs’ “British Desmidaceæ”; Smith’s “British Diatomaceæ”;
Goebel’s “Outlines of Classification and Special Morphology”;
Berkeley’s “Cryptogamic Botany”; De Bary’s “Comparative
Anatomy of the Phaneragams and Ferns”; Professor Marshall
Ward’s “Sach’s Physiology of Plants,” and numerous memoirs
on Fungi; and Bower and Sidney Vine’s “Course of Practical
Instruction in Botany,” a most instructive book on the histology
of plants.
63 “A Manual of the Infusoria,” by W. Saville Kent, F.L.S., &c.,
1880.
64 “Journal of the Linn. Society,” vol. viii., p. 202; vol. ix., p. 147,
1865 and 1866.
tissue must be kept in alcohol exposed to light, until the whole
of the chlorophyll is dissolved out; it must then be treated for
several hours in a strong solution of potash. After neutralisation
with acetic acid, the tissue may be treated with iodine, which
colours it blue, or with coralline solution, which colours it pink.
58 Verhandl. d. Natur. Hist. Jahr. xx. p. 1. “Micros. Jour. Science,”
vol. iii., p. 120.
59 For instance, where the yellow Palmella is found the
Chlorococcus will assume a yellow tinge in its soridial stage.
Viewed by transmitted light the sori are seen as opaque balls,
with an irregular outline.
60 “Contributions to the Knowledge of the Development of the
Gonidia of Lichens.” By J. Braxton Hicks, M.D., “Quarterly
Journal of Microscopical Science,” vol. viii., 860, p. 239.
61 Berkeley’s “Introduction to Cryptogamic Botany,” 1857.
62 For more detailed information on the structure and classification
of unicellular plants, and cryptogams, the reader is referred to
Ralfs’ “British Desmidaceæ”; Smith’s “British Diatomaceæ”;
Goebel’s “Outlines of Classification and Special Morphology”;
Berkeley’s “Cryptogamic Botany”; De Bary’s “Comparative
Anatomy of the Phaneragams and Ferns”; Professor Marshall
Ward’s “Sach’s Physiology of Plants,” and numerous memoirs
on Fungi; and Bower and Sidney Vine’s “Course of Practical
Instruction in Botany,” a most instructive book on the histology
of plants.
63 “A Manual of the Infusoria,” by W. Saville Kent, F.L.S., &c.,
1880.
64 “Journal of the Linn. Society,” vol. viii., p. 202; vol. ix., p. 147,
1865 and 1866.
Page 849
65 Among the more important works on Foraminifera for
consultation will be found D’Orbigny’s “Foraminiferes Fossiles
du Bassin Tertiaire de Vienne” (Autriche); Schultze, “Ueber den
Organismus der Polythalamien,” 1854; Carpenter and
Williamson’s “Researches on the Foraminifera,” “Phil. Trans.
1856;” Parker and Rupert-Jones in the “Annals of Natural
History.” Specimens of Foraminifera may be obtained by
shaking dried sponges; but if required alive they must be
dredged for, or picked off the fronds of living seaweeds, over
the surface of which they are, by the aid of a lens, seen to move.
66 W. Saville Kent, F.L.S., Op. Cit., p. 335.
67 Difficulties formerly associated with the microscopic
examination of flagellate forms of infusorial life have been
overcome by improvements in the objectives, by the knowledge
gained of the monad groups, and by the exhaustive researches of
Drs. Drysdale and Dallinger, whose joint investigations were
published in the Journal of the Royal Microscopical Society,
1873-75. By employing the highest and most perfectly
constructed powers of the microscope, and devoting an
enormous amount of time and attention to unravelling mysteries
so long associated with the production of the lowly organised
flagellate organisms, monads, and patiently watching hour by
hour, the life-history of numerous species of these minute
infusorial animalcules were obtained. Not only was it
discovered that these organisms increased indefinitely by
fission, but that under certain conditions two or more
individuals were united into encystments, and whose contents
broke up into a greater or less number of spore-like bodies, were
speedily developed into the parent type. In the examination of
these minute bodies, it has been found that talc-films, that is,
talc split into extremely fine laminæ, offer the best kind of
cover, in fact, supersede ordinary glass covers, and possess an
advantage, that of bending readily, thus permitting the objective
to be brought close down upon the object.
consultation will be found D’Orbigny’s “Foraminiferes Fossiles
du Bassin Tertiaire de Vienne” (Autriche); Schultze, “Ueber den
Organismus der Polythalamien,” 1854; Carpenter and
Williamson’s “Researches on the Foraminifera,” “Phil. Trans.
1856;” Parker and Rupert-Jones in the “Annals of Natural
History.” Specimens of Foraminifera may be obtained by
shaking dried sponges; but if required alive they must be
dredged for, or picked off the fronds of living seaweeds, over
the surface of which they are, by the aid of a lens, seen to move.
66 W. Saville Kent, F.L.S., Op. Cit., p. 335.
67 Difficulties formerly associated with the microscopic
examination of flagellate forms of infusorial life have been
overcome by improvements in the objectives, by the knowledge
gained of the monad groups, and by the exhaustive researches of
Drs. Drysdale and Dallinger, whose joint investigations were
published in the Journal of the Royal Microscopical Society,
1873-75. By employing the highest and most perfectly
constructed powers of the microscope, and devoting an
enormous amount of time and attention to unravelling mysteries
so long associated with the production of the lowly organised
flagellate organisms, monads, and patiently watching hour by
hour, the life-history of numerous species of these minute
infusorial animalcules were obtained. Not only was it
discovered that these organisms increased indefinitely by
fission, but that under certain conditions two or more
individuals were united into encystments, and whose contents
broke up into a greater or less number of spore-like bodies, were
speedily developed into the parent type. In the examination of
these minute bodies, it has been found that talc-films, that is,
talc split into extremely fine laminæ, offer the best kind of
cover, in fact, supersede ordinary glass covers, and possess an
advantage, that of bending readily, thus permitting the objective
to be brought close down upon the object.
Page 850
68 R. Kirkpatrick, Warne, Op. Cit., pp. 532-3.
69 Saville Kent, op. cit., p. 191.
70 Fritz Müller first demonstrated a nervous system in the Polyzoa:
—“The nervous system of each branch consisting of—1st, a
considerable sized ganglion situated at its origin; 2nd, of a
nervous trunk running the entire length of the branch, at the
upper part of which it subdivides into branches, going to the
ganglia of the internodes arising at this part; and 3rd, of a rich
nervous plexus resting on the trunk, and connecting the ganglia
just mentioned, as well as the basal ganglia of the individual
polypides.” For further account, see paper in the “Micros.
Journ.,” vol. i., New Series, p. 330.
71 I have ventured to devote some considerable space to the
development of the pond-snail, and for an obvious reason, that
of making it perfectly clear to my readers that my microscopical
investigations of Limnœa, made in 1853, were published in the
“Journal of the Microscopical Society,” June, 1854, and
republished in extenso in the several editions of this book,
dating from the last mentioned period. Nevertheless, the fringe
of cilia was, it appears, rediscovered in 1874, just twenty years
after my paper was published. It is almost unnecessary to add
that Carpenter gravely errs in his statement “that the existence of
the fringe of cilia in the embryo snail had been overlooked until
1874.”
72 Mr. George Rainey many years ago made us acquainted with the
fact that certain of the appearances presented by the shell or
other hard structures of animals, and which had hitherto been
referred to as cell-development, are really governed by the
physical laws which govern the aggregation of certain
crystalline salts when exposed to the action of vegetable and
animal substances in a state of solution. Mr. Rainey furnished a
process for obtaining artificially a crystalline substance which
shall so closely resemble shell structure that it can barely be
distinguished from it. The chemical substances to be used in the
69 Saville Kent, op. cit., p. 191.
70 Fritz Müller first demonstrated a nervous system in the Polyzoa:
—“The nervous system of each branch consisting of—1st, a
considerable sized ganglion situated at its origin; 2nd, of a
nervous trunk running the entire length of the branch, at the
upper part of which it subdivides into branches, going to the
ganglia of the internodes arising at this part; and 3rd, of a rich
nervous plexus resting on the trunk, and connecting the ganglia
just mentioned, as well as the basal ganglia of the individual
polypides.” For further account, see paper in the “Micros.
Journ.,” vol. i., New Series, p. 330.
71 I have ventured to devote some considerable space to the
development of the pond-snail, and for an obvious reason, that
of making it perfectly clear to my readers that my microscopical
investigations of Limnœa, made in 1853, were published in the
“Journal of the Microscopical Society,” June, 1854, and
republished in extenso in the several editions of this book,
dating from the last mentioned period. Nevertheless, the fringe
of cilia was, it appears, rediscovered in 1874, just twenty years
after my paper was published. It is almost unnecessary to add
that Carpenter gravely errs in his statement “that the existence of
the fringe of cilia in the embryo snail had been overlooked until
1874.”
72 Mr. George Rainey many years ago made us acquainted with the
fact that certain of the appearances presented by the shell or
other hard structures of animals, and which had hitherto been
referred to as cell-development, are really governed by the
physical laws which govern the aggregation of certain
crystalline salts when exposed to the action of vegetable and
animal substances in a state of solution. Mr. Rainey furnished a
process for obtaining artificially a crystalline substance which
shall so closely resemble shell structure that it can barely be
distinguished from it. The chemical substances to be used in the
Page 851
preparation of the artificial shell, or calculi, are a soluble
compound of lime and carbonate of potash or soda, dissolved in
separate portions of water, and mixed with some viscid
vegetable or animal substance, as gum or albumen, and mixing
the several solutions together. The mechanical conditions
required are that such a quantity of each of the viscid materials
in each solution shall be of about the same density as that of the
nascent carbonate of lime, and at perfect rest. This state of rest
will require from two to three weeks or longer. Mr. Rainey
shows the analogy or identity of his artificially formed crystals
with those found in natural products both in animals and
vegetables, chiefly confining himself to the structure and
formation of shells and bone, pigmental and other cells, and the
structure and development of the crystalline lenses, which he
contends are all formed upon precisely the same physical
principles as the artificial crystals.
73 E. Ray Lankester, “On the Gregarinæ found in the common
Earthworm.”—“Micros. Trans.” vol. iii. p. 83.
74 For the fullest information of marine, land, and fresh-water
species, consult Dr. Bastian’s “Monograph on the
Anguillulidæ”; “Lin. Soc. Trans.” vol. xxv. p. 75; the
“Anguillula Aceti,” by the author, in the “Popular Science
Review,” January, 1863.
75 “Cercaria parasitic on Limnœa,” “Jour. Royal Micros. Soc.”
1870.
76 See my paper “The Natural History of a Nematode Worm,”
“Journ. of Microscopy and Natural History,” October, 1888.
77 “The Parasites of Man and the Diseases which proceed from
them,” by Professor Rudolf Leuckart, 1886.
78 R. J. Pocock, “On Worms” (Warne, Op. cit.), p. 465.
compound of lime and carbonate of potash or soda, dissolved in
separate portions of water, and mixed with some viscid
vegetable or animal substance, as gum or albumen, and mixing
the several solutions together. The mechanical conditions
required are that such a quantity of each of the viscid materials
in each solution shall be of about the same density as that of the
nascent carbonate of lime, and at perfect rest. This state of rest
will require from two to three weeks or longer. Mr. Rainey
shows the analogy or identity of his artificially formed crystals
with those found in natural products both in animals and
vegetables, chiefly confining himself to the structure and
formation of shells and bone, pigmental and other cells, and the
structure and development of the crystalline lenses, which he
contends are all formed upon precisely the same physical
principles as the artificial crystals.
73 E. Ray Lankester, “On the Gregarinæ found in the common
Earthworm.”—“Micros. Trans.” vol. iii. p. 83.
74 For the fullest information of marine, land, and fresh-water
species, consult Dr. Bastian’s “Monograph on the
Anguillulidæ”; “Lin. Soc. Trans.” vol. xxv. p. 75; the
“Anguillula Aceti,” by the author, in the “Popular Science
Review,” January, 1863.
75 “Cercaria parasitic on Limnœa,” “Jour. Royal Micros. Soc.”
1870.
76 See my paper “The Natural History of a Nematode Worm,”
“Journ. of Microscopy and Natural History,” October, 1888.
77 “The Parasites of Man and the Diseases which proceed from
them,” by Professor Rudolf Leuckart, 1886.
78 R. J. Pocock, “On Worms” (Warne, Op. cit.), p. 465.
Page 852
79 An interesting account of the formation of the tubes of Serpula is
given by Mr. Watson, “Jour. Micros. Soc.,” vol. 1890, p. 685.
80 Dr. Baird, “Natural History of British Entomostraca,” printed for
the Ray Society, 1850.
81 See Mr. B. T. Lowne’s exhaustive treatise on “The Anatomy and
Physiology of the Blow-fly,” a volume of 750 pages and 52
plates, 1891.
82 Tuffen West, “Trans. Linn. Soc.,” vol. xxiii., p. 393.
83 The term micropyle (a little gate) has heretofore only been used
in its relation with the vegetable kingdom: it is used to denote
the opening or foramen towards which the radicle is always
pointed.
84 Dr. Halifax adopts the method of killing the insect with
chloroform; he then immerses it in a bath of hot wax, in which it
is allowed to remain until the wax becomes cold and hard; with
a sharp knife sections are easily made in the required direction
without in the least disturbing any of the more fragile parts, or
internal organs of the specimen.
85 “Phil. Trans.,” 1859, p. 341.
86 See my paper on “The Eggs of Insects,” in “The Intellectual
Observer,” Oct. 1867, in which other varieties of eggs are given.
87 W. U. Whitney, “Transactions of the Microscopical Society” for
1861 and 1867.
88 Mr. F. G. Cuttell, 52, New Compton Street, Soho, cuts and
prepares excellent sections.
89 Published with his paper in detail, “Aperture as a Factor in
Microscopic Vision,” “Journal of Royal Micros. Soc.,” June,
1808, pp. 334 et seq.
given by Mr. Watson, “Jour. Micros. Soc.,” vol. 1890, p. 685.
80 Dr. Baird, “Natural History of British Entomostraca,” printed for
the Ray Society, 1850.
81 See Mr. B. T. Lowne’s exhaustive treatise on “The Anatomy and
Physiology of the Blow-fly,” a volume of 750 pages and 52
plates, 1891.
82 Tuffen West, “Trans. Linn. Soc.,” vol. xxiii., p. 393.
83 The term micropyle (a little gate) has heretofore only been used
in its relation with the vegetable kingdom: it is used to denote
the opening or foramen towards which the radicle is always
pointed.
84 Dr. Halifax adopts the method of killing the insect with
chloroform; he then immerses it in a bath of hot wax, in which it
is allowed to remain until the wax becomes cold and hard; with
a sharp knife sections are easily made in the required direction
without in the least disturbing any of the more fragile parts, or
internal organs of the specimen.
85 “Phil. Trans.,” 1859, p. 341.
86 See my paper on “The Eggs of Insects,” in “The Intellectual
Observer,” Oct. 1867, in which other varieties of eggs are given.
87 W. U. Whitney, “Transactions of the Microscopical Society” for
1861 and 1867.
88 Mr. F. G. Cuttell, 52, New Compton Street, Soho, cuts and
prepares excellent sections.
89 Published with his paper in detail, “Aperture as a Factor in
Microscopic Vision,” “Journal of Royal Micros. Soc.,” June,
1808, pp. 334 et seq.
Page 853
90 “Squire’s Methods and Formulæ;” “Modern Microscopy,” Cross
and M. F. Cole; “The Microscopists’ Vade Mecum,” A. B. Lee;
“Bacteriology.” Professor Dr. E. Crookshank, Messrs. Baird and
Tattock, Cross Street, Hatton Garden, supply all Scientific
Apparatus for Bacteriological Work.
91 The imperial gallon contains 277.27384 cubic inches, and the
imperial pint 20 fluid ounces, whereas the wine gallon has 231
cubic inches and the pint 16 fluid ounces. In wine measure 1
litre = 33.815 fluid ounces.
Transcriber’s Note:
Page xxiii, “l. Corystes cossivelaunus” changed to read “l. Corystes
cassivelaunus”.
Page xxv ERRATA incorporated into project.
Page xix, “Acmeœa virginea, part of palate—118.” changed to read
“Acmæa virginea, part of palate—118.”
Page 21, “in Fig. 13, if S, S′ are a pair of conjugate foci,” changed to
read “in Fig. 12, if S, S′ are a pair of conjugate foci,”. S and S′ are in
Fig. 12.
Page 89 “Bacteriological and Histol gical” changed to read
“Bacteriological and Histological”.
Page 598, “Apis nillifica” changed to read “Apis mellifica”, also entry
in index.
Page 663, “the papillæ of the tongue is distended and seen erect”
changed to read “the papillæ of the tongue are distended and seen
and M. F. Cole; “The Microscopists’ Vade Mecum,” A. B. Lee;
“Bacteriology.” Professor Dr. E. Crookshank, Messrs. Baird and
Tattock, Cross Street, Hatton Garden, supply all Scientific
Apparatus for Bacteriological Work.
91 The imperial gallon contains 277.27384 cubic inches, and the
imperial pint 20 fluid ounces, whereas the wine gallon has 231
cubic inches and the pint 16 fluid ounces. In wine measure 1
litre = 33.815 fluid ounces.
Transcriber’s Note:
Page xxiii, “l. Corystes cossivelaunus” changed to read “l. Corystes
cassivelaunus”.
Page xxv ERRATA incorporated into project.
Page xix, “Acmeœa virginea, part of palate—118.” changed to read
“Acmæa virginea, part of palate—118.”
Page 21, “in Fig. 13, if S, S′ are a pair of conjugate foci,” changed to
read “in Fig. 12, if S, S′ are a pair of conjugate foci,”. S and S′ are in
Fig. 12.
Page 89 “Bacteriological and Histol gical” changed to read
“Bacteriological and Histological”.
Page 598, “Apis nillifica” changed to read “Apis mellifica”, also entry
in index.
Page 663, “the papillæ of the tongue is distended and seen erect”
changed to read “the papillæ of the tongue are distended and seen
Page 854
erect”.
Obvious printer errors corrected silently.
Inconsistent spelling and hyphenation are as in the original.
Obvious printer errors corrected silently.
Inconsistent spelling and hyphenation are as in the original.
Page 855
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