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The Project Gutenberg eBook of The anatomy of the domestic
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Title: The anatomy of the domestic fowl

Author: B. F. Kaupp

Release date: August 8, 2023 [eBook #71368]

Language: English

Original publication: Philadelphia: W. B. Saunders Company, 1918

Other information and formats: www.gutenberg.org/ebooks/71368

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*** START OF THE PROJECT GUTENBERG EBOOK THE ANATOMY
OF THE DOMESTIC FOWL ***

Transcriber’s Note:

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New original cover art included with this eBook is
granted to the public domain.

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The Anatomy
of the
Domestic Fowl

By
B. F. Kaupp, M. S., D. V. M.
Poultry Investigator and Pathologist in the North Carolina Experiment Station, State
Department of Agriculture, and the State College of Agriculture; Formerly Director of
Anatomy Laboratory, Kansas City Veterinary College

Illustrated

Philadelphia and London

W. B. Saunders Company
1918

Page 6

Copyright, 1918, by W. B. Saunders Company

PRINTED IN AMERICA

To
DAN T. GRAY, B. S., A. B., M. S.
Chief, Animal Industry Division, North Carolina
Experiment Station
As a Token of Respect and Gratitude This
Volume is Dedicated
By
THE AUTHOR

Page 7

FOREWORD

Advanced work in the study of poultry husbandry is now being done in
this country, to a greater or less extent, at all the two score and more
Agricultural and other Colleges and Experiment Stations. From these
institutions comes the demand for a text-book on the Anatomy of the
Domestic Fowl. No complete text-book on the subject, up to the present,
has existed. It is with the hope of meeting the demand that this book is
published.
In supplementing the information gathered from the books and articles
listed in the bibliography, the author has spent much time and effort in
obtaining the matter here presented. As this, however, is the initial complete
text on the subject necessarily much remains to be added and corrected. The
author would welcome suggestions and corrections from any one into
whose hands the book may come.
B. F. Kaupp.

The North Carolina State College of Agriculture,
West Raleigh, North Carolina,
September, 1918.

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CONTENTS

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OSTEOLOGY

Page
Osseous Structure 17
Classification of Bones 20
Composition of Bone 21
Skeleton of the Fowl 21
Axial Skeleton 23
Cranium and Face 23
Occipital 25
Ethmoid 27
Sphenoid 28
Frontal 29
Parietal 29
Temporal 29
Premaxilla 31
Maxilla 32
Nasal 32
Lacrimal 32
Palatine 33
Pterygoid 33
Zygomatic 33
Vomer 33
Jugal and Quadrato-jugal 33
Quadrate 34
Inferior Maxilla 34
Turbinate Bones 34
Hyoid 35
Vertebral Column 35
Cervical Vertebræ 35
Atlas 37
Axis 37
Dorsal Vertebræ 39
Lumbo-sacral Vertebræ 39
Coccygeal Vertebræ 41
Ribs 41
Sternum 42
Appendicular Skeleton 43
Shoulder Girdle 43
Fore Limb 44

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Pelvic Girdle 48
Hind Limb 50

ARTHROLOGY
Kinds of Joints 56
Movements of Joints 56
Ligamentous Structure 57
Ligaments of:
Ear 58
Jaw 58
Vertebræ 58
Ribs 59
Sternum 59
Shoulder-joint 61
Elbow-joint 61
Carpal Joint 62
Finger 64
Pelvis 65
Hip-joint 65
Knee-joint 65
Tibio-metatarsal Joint 69
Toes 69

MYOLOGY
Kinds and Structure of Muscles 70
Fascia 71
Muscular Nomenclature 71
True Dermal Muscles 71
Dermo-osseous Muscles 73
Muscles of the Head 76
Muscles of the Tongue 79
Cervical Muscles 81
Muscles of the Air Passages 86
Superior Larynx 86
Inferior Larynx 86
Sternal Muscles 90
Abdominal Muscles 90
Dorsolumbar Muscles 92
Coccygeal Muscles 93
Costal Muscles 96
Anterior Pectoral Muscles 99

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Pectoral Muscles 100
Muscles of the Scapular Region 101
Muscles of the Brachial Region 104
Muscles of the Forearm and Hand 105
Digital Muscles 109
Muscles of the Posterior Limb 111
Tibial Group of Muscles 117
Muscles of the Eye 124
Muscles of the Ear 128
Functions of Muscles 128

SPLANCHNOLOGY
Digestive Apparatus 135
Mouth 135
Tongue 139
Pharynx 141
Glands Adjacent to Mouth and Pharynx 141
Esophagus 142
Crop 142
Stomach 143
Proventriculus 143
Gizzard 145
Small Intestine 147
Large Intestine 150
Cæca 151
Cloaca 151
Course of the Food 152
Accessory Organs of Digestion 152
Liver 153
Pancreas 155
Spleen 155
Abdominal and Pelvic Cavities 156
Peritoneum and Mesentery 156
Relations of the Visceral Organs of the Domestic Fowl 158
Relations of the Visceral Organs of the Baby Chick 165
Uro-genital System 169
Urinary Apparatus 169
Kidneys 169
Ureter 174
Male Generative Organs 175
Testicles 175

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Vas Deferens 178
Female Generative Organs 178
Egg 180
Oviduct 182
Parts of the Oviduct 183
Ligaments of the Oviduct 188
Ductless Glands 190
Thyroid Gland 190
Thymus Gland 190
Adrenal Gland 191
Respiratory Apparatus 193
Nostrils and Nasal Chambers 193
Pharynx and Superior Larynx 193
Trachea 194
Inferior Larynx 194
Bronchi and the Lungs 195
Air-sacs 199

ANGIOLOGY
Circulatory Apparatus 206
Heart 206
Structure of the Heart 207
Blood-vessels 209
Structure of the Capillaries and Arteries 209
Structure of the Veins 211
Arterial Trunks 211
Branches of:
Arteria Brachiocephalica 213
Arteria Carotis Cerebralis Interna 214
Arteria Carotis Externa 214
Arteria Carotis Facialis 214
Aorta Posterior 224
Venous Trunks 233
Branches of:
Venæ Cavæ Anteriores 234
Vena Jugularis 237
Vena Occipitalis Externa 239
Venous Sinuses of the Head 239
Veins of the Brain Cavity 241
Veins of the Neck 242
Branches of the Vena Subclavia 243

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Veins of the Dorsal Region 243
Veins of the Thorax 244
Veins of the Fore Limb 245
Branches of the Iliaca 246
Branches of the Vena Iliaca Interna 247
Posterior Vena Cava 247
Veins of the Posterior Extremity 248
Branches of the Vena Cava Posterior 248
Veins of the Caudal Region and Pelvic Cavity 250
Veins of the Truncus Vena Iliaca Communis 252
Visceral Veins of the Posterior Vena Cava 252
Lymphatic System 254
Blood and its Functions 257
Fate of the Erythrocyte 261

NEUROLOGY
Nervous System 264
Cranial Nerves 265
Olfactorius 265
Opticus 267
Motoris Oculi 267
Patheticus 268
Trifacialis 268
Abducentes 270
Facialis and Acousticus 271
Vagus Group 272
Glosso-pharyngeus 272
Vagus or Pneumogastricus 273
Accessorius Spinalis 274
Hypoglossus 274
Spinal Cord 275
Structure of the Cord 275
Structure of the Nerve Trunks and Ganglia 277
Spinal Nerves 281
Brachial Plexus 282
Lumbo-sacral or Crural Plexus 285
Brain 288
Coverings of the Brain 288
Structure of the Brain 289
Divisions of the Brain 290
Sympathetic Nervous System 297

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Functions of the Nervous System 300

ESTHESIOLOGY
Sense Organs 303
Sight 303
Hearing 305
Smell 307
Taste 307
Touch 307
Structure of Appendages 309

EMBRYOLOGY
Spermatogenesis 318
Oögenesis 319
Fertilization 319
Outline for Laboratory Study of the Chick 330
Living Embryo 330
Preparation for Study of Entire Embryos and Sections 330
Points to be Observed in the Study 332
Derivatives of the Germ-layers 342
Preparation of Structures for Study 343
Directions for Dissecting Muscles 343
Directions for Study of the Viscera 344
Directions for Study of the Arteries 345
Study of the Structure of Bones 346
Special Technic for Dissection of Cranial and Spinal Nerves 347
Directions for Study of Soft Structures 347
To Stain Sections of Liver for Study of Kupffer Cells 349
To Prepare Anatomical Specimens for Museum 349
To Make Specimens Transparent 350
Equipment for the Dissection Laboratory 351

Bibliography 353
Index 355

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ANATOMY
OF THE
DOMESTIC FOWL

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OSTEOLOGY

Osseous Structure.—Bone is structurally modified connective tissue which has
become hard by being impregnated with calcium salts.
Kinds of Bone Tissue.—There are two kinds of bone tissue: substantia compacta, or
compact bone tissue; and substantia spongiosa, or spongy, cancellous bone tissue.
Compact Bone Tissue.—The compact bone tissue forms the hard outer layer of all
bones. It is thickest in the shaft and becomes thin toward the extremities. Through the
compact bone tissue approximately parallel with the longitudinal axis of the bone, run
canals called Haversian canals, through which pass blood and lymph vessels for the
nourishment of the bone and nerves. The Haversian canals are surrounded by concentric
lamellæ. The spaces between the cylinders thus formed are filled with interstitial lamellæ;
and both the exterior surface of the bone and the interior surface surrounding the
medullary canal, are built up of peripheral, or circumferential lamellæ. Between the
lamellæ, somewhat irregularly placed, are minute reservoirs, called lacunæ, which contain
bone corpuscles. From the lacunæ radiate minute canals, or canaliculi, which maintain
circulation through the bone substance, and which communicate with the Haversian
canals. Complex anastomoses exist among the canaliculi. Still other channels for the
passage of blood-vessels are Volkmann’s canals which pierce the peripheral lamellæ, thus
allowing vessels to pass from the periosteum to the Haversian canals. Similar channels
afford communication between the inner Haversian canals and the medullary cavity.
The entire structure composed of an Haversian canal, its surrounding lamellæ, lacunæ,
and canaliculi, with their contained vessels, is called an Haversian system.
Cancellous Bone Tissue.—The cancellous bone tissue forms the bulk of the short, flat,
and irregular bones and of the extremities of the long bones. It consists of delicate bony
plates and spicules, which intercross in various directions. The spaces between these
plates and spicules, called cancelli, are occupied by marrow except in the bones that are
pneumatic. The blood-vessels, lymphatics, and nerves course through this marrow but are
not arranged in an Haversian system.

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Fig. 1.—Longitudinal section of compact bone
of the femur of the hen. 1, Haversian canals. 2,
Lacunæ with their canaliculi.

The Periosteum.—Covering the surface of bone, except at the articular surface where it
is covered with cartilage, is a membrane, the periosteum, which consists of two layers: an
outer, fibrous, protective layer, and an inner, cellular, osteogenic layer. The outer layer
consists principally of white fibrous tissue. The inner layer contains many more
connective-tissue cells, which gradually become more closely aggregated as we proceed
toward the osseous surface; but there is no sharply defined line of demarcation between
the two periosteal layers.

Fig. 2.—Transverse section of compact bone of
the femur of the hen. 1, The lacunæ and
canaliculi. 2, The periosteum.

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Fig. 3.—Transverse section of compact bone of
the femur of the hen showing the lacunæ and
canaliculi under high magnification.

The periosteum is firmly attached to the bone by trabeculæ of fibrous tissue, called the
fibers of Sharpey. These fibers of Sharpey penetrate the bone at right angles to its surface
and carry blood-vessels.
Marrow.—There are two kinds of marrow: yellow, or medulla ossium flava, and red, or
medulla ossium rubra.
The yellow marrow occurs in all bones except the femur and proximal portion of the
tibia of adult fowls. It is composed of a network of fibrous tissue carrying blood-vessels,
fat cells, and myelocytes, or marrow cells.
The red marrow is found throughout the femur and the proximal portion of the tibia,
and in a few of the pelvic bones and vertebræ in the adult fowl, and in certain other bones
of the baby chick. Red marrow consists of a delicate network of connective tissue
supporting a dense capillary plexus, a small amount of fat, and numerous cells. The
cellular elements of red marrow consist of marrow cells which contain large nuclei and
possess ameboid movement, red blood cells, giant cells containing one or more nuclei, and
various kinds of leucocytes, including eosinophiles, mast cells, and also osteoclasts.
Growth of Bone.—In the baby chick, only the shaft and a portion of the extremities of
the long bones are thoroughly ossified, the extreme ends, and of the femur most of the
articular head, being cartilaginous. The bones grow in length by an increase in the
cartilage, the cartilage gradually becoming ossified. Growth in diameter is accomplished
by the constant deposition of new layers of bone beneath the periosteum. During this
process the osteoclasts absorb the bone from within. The formation of the marrow cavity
is thus effected.

Classification of Bones.—The bones of the fowl are classified as long, short, flat, and
irregular.
Long Bones.—The long bones occur in the legs and wings, where they serve as levers
to sustain weight and make locomotion possible. A long bone consists of a shaft and two

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extremities. The superior is called the proximal and the inferior the distal extremity. The
expanded articular surfaces in forming joints with adjoining bones afford ample space for
the attachment of ligaments. The shaft is cylindrical and hollow.
Short Bones.—Short bones occur in the feet and in the wings. Their structure is similar
to that of the long bones.
Flat Bones.—The flat bones occur where extensive protection is needed, as in the
cranial region; or where large surface for muscular attachments is needed, as in the costal
and pelvic regions. Flat bones are made up of two thin layers of compact bone with a
variable amount of cancellous tissue interposed.
Irregular Bones.—The irregular bones include the vertebræ, the patellæ, and the carpal
bones.

Composition of Bone.—Bone consists of organic and inorganic matter. Organic matter
gives toughness and elasticity to the bone, and inorganic matter hardness. The organic
substance of bone is called ossein. When boiled in water ossein is resolved into gelatin.
The following tables[1] give the results of an analysis of the femur, fresh, of a mature hen.
1. Grateful acknowledgment is hereby made to Dan M. McCarty, Chemist, Animal Industry Division, North
Carolina Agricultural Experiment Station, for this analysis.

Fresh femur:
Water 18.23 per cent.
Dry matter 81.77 per cent.
Dry matter:
Organic matter 63.09 parts
Inorganic matter 18.68 parts
Salts in dry matter:
Calcium 6.970 per cent.
Magnesium 0.283 per cent.
Potassium 0.004 per cent.
Sodium 0.276 per cent.
Iron 0.020 per cent.
Phosphorus 3.210 per cent.
Sulphur 0.085 per cent.
Chlorine 0.520 per cent.
Carbon dioxid 0.550 per cent.

The inorganic matter of the femur of the hen consists of 18.68 parts or 22.84 per cent.
of dry matter, and the organic matter of 77.16 per cent. Stated in other words the femur,
including its contained marrow, consists of organic and inorganic matter in the ratio of 3.4,
approximately, to 1.

The Skeleton of the Fowl.—The skeleton of a bird is remarkable for the rapidity of its
ossification. It is worthy of note that other parts of the bodies of adult birds also become

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ossified. Among such parts are the tendons of the muscles of the legs, of the feet, and of
the neck; the plates of the corneal margin of the sclerotic tunic of the eye; and the stapes
of the ear. Ossification in birds at the attachments of the semi-lunar valves of the aorta and
of the pulmonary artery has been reported by Owen.
The bony structure is compact, and the bones contain a greater proportion of phosphate
of lime than do the osseous structures of mammals. Especially is this the case in those
parts of the skeleton which are permeated by air.

The Divisions of the Skeleton

( The Skull ( Cranium

( ( Face

The Axial skeleton ( ( Cervical region

( ( Dorsal region ( Ribs

( The Vertebral column ( ( Sternum

( Lumbar region

( Sacral region

( Coccygeal region

( Scapula

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( Shoulder girdle ( Coracoid

( ( Clavicle

(

( ( Arm ( Humerus

( (

( Fore limb ( Forearm ( Radius

( ( ( Ulna

( (

( ( ( Carpus

The Appendicular skeleton ( ( Hand ( Metacarpus

( ( Phalanges

(

( Pelvic girdle ( Ilium

( (Hip bone) ( Ischium

( ( Pubis

(

( ( Thigh ( Femur

( Hind limb (

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( Leg ( Tibia

( ( Fibula

(

( Foot ( Metatarsus

( Phalanges

The bodies of birds contain many air reservoirs to make them light that flying may be
more easy. Many bones have their weight in proportion to size and strength thus greatly
reduced. In very young birds the cavities of bones contain, instead of air spaces, loosely
arranged red marrow, which is in most bones later absorbed. The air reservoirs in bones
are most capacious in the best flyers. In the non-flyers more of the bones retain their red
marrow.
The bones supplied with air spaces are relatively larger than in mammals, and are
provided with small transverse osseous columns which cross in different directions and
from side to side. These cross beams give stability to the thin wall of the bone. The
membranes lining these cavities are very vascular.

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The Axial Skeleton

THE SKULL

The skull is divided into the cranial and facial portions. In these parts we find present
31 bones: one occipital, two parietal, two frontal, one ethmoid, one sphenoid, and two
temporal; all of which constitute the cranial group; two premaxillary, two maxillæ, two
nasal, two lacrimal, two palatine, two pterygoid, two zygomatic, one vomeral, the two
jugal, and two quadrato-jugal, which constitute the facial group; two quadrati and one
inferior maxillary, which constitute the inferior jaw group.
The peculiarities of the skull are the long os incisivum and the single condyle located
on the occipital bone just below the foramen magnum. The condyle articulates with the
atlas.
The head of the bird is small in proportion to the size of the body, and in front it is
conical in shape.

The Cranium

The cranial cavity, or cavum cranii, incloses the brain with its membranes and vessels.
The dorsal wall, or roof, is formed by the frontal and the parietal bones. In the median
line of the cerebral portion is the internal parietal crest. The roof of the cerebellar portion
is marked centrally by a groove.
The posterior wall of the cerebellum is formed by the occipital bone.
The lateral wall is formed chiefly by the temporal bone. It is marked by a ridge which
divides the cavity into the cerebral and cerebellar compartments. The cerebral portion is
marked by a depression which receives the optic lobes. A crest divides this cavity from the
optic portion. The walls are marked by digitations and vascular grooves.

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Fig. 4.—The skeleton of the domestic fowl. 1,
Os incisivum. 2, External nasal opening. 3, Os
nasale. 4, Os lachrymale. 5, Lamina
perpendicularis. 6, Os dentale. 7, Os palatine. 8,
Os quadrato-jugal. 9. Os pterygoideum. 10, Os
quadratum. 11, Os articulare. 12, External
auditory canal. 13, Atlas. 14, Os carpi radiale.
15, Radius. 16, First finger. 17, Os metacarpus.
18, Second finger. 19, Third finger. 20, Os carpi
ulnare. 21, Ulna. 22, Humerus. 23, Thoracic
vertebræ. 24, Scapula. 25, Os ilium. 26,
Foramen ischiadicum. 27, Caudal vertebræ. 28,
Pygostyle. 29, Foramen obturatum. 30, Os
ischium. 31, Processus uncinatus. 32, Vertebral
rib. 33, Os claviculum or furculum. 34, Os
coracoideum. 35, Os femoris. 36, Os pubis. 37,
Body of sternum. 38, Lateral internal process of
sternum. 39, Costal process of sternum. 40,
Sternal crest, cristi sterni, or keel of breast-
bone. 41, Sternal rib. 42, Lateral external
process of sternum. 43, Os fibula. 44, Xyphoid
process of sternum. 45, Internal notch. 46, Os
patella. 47, Os tibia. 48, Os metatarsus. 49,
Second toe. 50, Fourth toe. 51, Os metatarsale.
52, First toe. 53, Second toe. 54, Second
phalanx of second finger. 55, Os metacarpus.
56, Air opening in humerus. 57, Hypocledium.
58, External notch. 59, Cervical vertebræ. 60,
Foramen oblongum.

The ventral wall, floor, or basis cranii interna, may be regarded as forming five fossæ.
These are: one anterior, one middle, one posterior, and two lateral. The anterior fossa

Page 25

supports the frontal and olfactory parts of the cerebrum. It lies at a higher level than the
middle fossa. The middle fossa, or fossa cranii media, is circular in outline and extends
into the lateral fossæ which lodge the olfactory lobes. Just back of the middle fossa is the
sulla turcica, upon which rests the pituitary body. The posterior fossa, or fossa cranii
posterior, lodges the medulla oblongata.

Bones of the Cranium (Figs. 4, 6, 7, and 8).—The bones of the cranium fuse early in
the chick’s life. The sutures uniting the bones can usually be seen in the fetus or in the
baby chick soon after it emerges from the shell. The major portion of the cranial bones
become entirely fused. Each cranial and each facial bone ossifies from a distinct center or
centers.
The cavity for the cerebrum is much larger than the cavity for the cerebellum. The
cranial cavities in birds are relatively larger than in mammals. The bones are designated as
in mammals. There are three single bones, the occipital, the ethmoid, and the sphenoid.
Those in pairs are the frontal, the parietal, and the temporal.

The Occipital. Location.—The occipital bone or os occipitale, is situated at the
posterior part of the cranium, of which it forms the posterior wall. This part is called the
base of the cranium. The occipital bone articulates with or touches inferiorly, the
sphenoid, laterally, the temporal, and superiorly, the parietal.
Development.—The occipital bone is developed from four centers of ossification; the
dorsal, or os occipitale superius, two lateral, or ossa occipitales laterales, and the ventral,
or os occipitale inferius, all of which may be seen distinct in the baby chick (Fig. 5, Part
II, No. 1).

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Fig. 5.—Bones of the head and vertebra.

Part I.—1, The cranium. 2, The skull cap. 3,
The ethmoid bone. 4, The inferior maxilla. 5,
The palatine bone. 6, The quadrato-jugal. 7, The
jugal. 8, The superior maxilla. 9, The
premaxilla. 10, The horny covering for the
premaxilla. 11, The horny covering for the os
dentale. 12, The os quadratum. 13, The nasal
bone. 14, The pterygoid.

Part II.—1, The os occipitale (1, dorsal; 2, two
lateral; 3, ventral portions and 4, foramen
magnum). 2, The fourteen cervical vertebræ. (1,
atlas; 2, axis). 3, The seven dorsal vertebræ. 4,
The fourteen lumbo-sacral vertebræ. 5, The
seven coccygeal vertebræ. 6, The pelvis (1,
ilium; 2, ischium; 3, pubis; 4, cotyloid cavity or
acetabulum). 7, The vertebral column complete
from the baby chick. 8, The parietal bone. 9,
The temporal bone. 10, The frontal bone.

Description.—In the center of the occipital bone is the foramen magnum. Through this
foramen the spinal cord extends into the cranial cavity and connects with the medulla
oblongata. The occipital bone has a single condyle, which is located just below the
foramen magnum and articulates with the atlas. At the base of the condyle a small
subcondyloid fossa receives the body of the atlas during extreme flexion of the head. In
the center of the lateral wing of the occipital bone there is a small foramen through which
passes the hypoglossal nerve. Somewhat laterally from this foramen there is an opening
through which the vagus, or pneumogastric nerve passes. Laterally from these is the
canalis caroticus et jugularis. Between the os occipitale superius, or dorsal portion, and
the ossa parietalia is a space to which ligaments are attached, called the fontanel.

Page 27

Fig. 6.—View of the frontal region of the skull
of a hen. 1, Parietal. 2, Frontal. 3, Nasal. 4,
Premaxilla. 5, Temporal. 6, Inferior jaw. 7,
Jugal bone.

The Ethmoid. Location.—The ethmoid, or os ethmoidale, forms the anterior wall of
the cranium, and the orbital septum. It is related anteriorly with the vomeral, superiorly
with the nasal and frontal, posteriorly with the temporal, and inferiorly with the sphenoid,
and palatine.
Description.—The ethmoid consists of a perpendicular and a horizontal lamina. The
perpendicular lamina, located between the orbital cavities, is called the septum
interorbitale. On each side of the septum interorbitale and near the superior orbital roof
are two foramina for the passage of the olfactory nerves. In the horizontal plate, which
forms the anterior cranial wall, are located the optic foramina through which pass the
optic nerves.

Page 28

Fig. 7.—Side view of the skull of a hen. 1, Lamina perpendicularis. 2, Foramen for the passage
of the nerve of smell. 3, Foramen for the passage of the optic nerve. 4, Nasal bone. 5, External
nasal opening. 6, Premaxilla. 7, Os dentale. 8, Superior maxilla. 9, Os jugal. 10, Os quadrato-
jugal. 11, Os quadratus. 12, Pterygoideus. 13, Os articulare. 14, Inferior maxilla. 15, Temporal.
16, External auditory canal. 17, Parietal. 18, Frontal. 19, Palatine. 20, Orbital process, posterior
to which is the processus zygomaticus. 21, Interorbital foramen and optic foramen for passage
of optic nerve. 22, Attachment for inferior oblique; 23, for superior oblique; 24, for levator
palpebræ superioris; 25, for internal rectus; 26, for superior rectus; 27, for external rectus; 28,
for inferior rectus; 28, for inferior rectus; 29, for depressor palpebræ inferioris; 30, for
orbicularis palpebrarum; 31, for tensor tympani; 32, for circumconcha.

The Sphenoid. Location.—The sphenoid, or os sphenoidale, forms the floor of the
cranial cavity and articulates with or touches posteriorly the occipital, laterally the
temporal, and anteriorly the palatine, and ethmoid.
Description.—The sphenoid bone, the largest part of the cranial floor, is formed by the
fusion of the nasal and the cranial parts. It is a three-cornered bone with two, thin, broad
wings. These wings are divided into two portions, orbital wings, or alæ orbitales, and
temporal wings, or alæ temporales. The temporal wing forms a cover for the Eustachian
tube trumpet, and for the canal coming from the sella turcica, which latter gives passage to
the intracranial carotid artery. The orbital wing forms the lower portion of the posterior
wall of the orbital cavity, and lies directly before the os petrosum or temporal bone where
the second and third branches of the fifth pair of cranial nerves emerge from the cranial
cavity.
Anteriorly the sphenoid has a foramen for the passage of the Eustachian tube, the tuba
auditiva, and also a sharp-pointed projection, the nasal portion, called the rostrum.

The Frontal. Location.—The frontal bones, or ossa frontales, two in number, form the
forehead, a portion of the nose, and a portion of the roof of the orbital cavities. They are
related posteriorly with the parietal, laterally with the temporal and zygomatic, and
anteriorly with the nasal and premaxillary. They touch inferiorly the ethmoid.

Page 29

Description.—Each of these bones has a processus orbitalis which is seen at the outer
margin of the posterior and upper orbital wall and just in front of the zygomatic process of
the squamous portion of the temporal. The frontal bone forms the anterior portion of the
superior wall of the cranial cavity. The two bones are thin, flat, and meet at the median
line of the forehead. The external surface is convex. The inner surface has a ridge located
longitudinally and in the center the bone becomes narrow anteriorly.

The Parietal. Location.—The parietal bones, or ossa parietalia, two in number, form
the posterior part of the roof of the cranial cavity. They meet in the median line and are
related posteriorly with the occipital, anteriorly with the frontal, and laterally with the
temporal bones.
Description.—The parietal bones are short and very broad (Fig. 5, Part II, No. 8). Each
bone is quadrilateral in outline and has two surfaces, four borders and four angles. The
external parietal surface is convex and smooth and the internal, cerebral surface is
concave.

The Temporal. Location.—The temporal bones, or ossa temporales, two in number, are
located at the lateral portion of the cranium, and aid in the formation of the cranial wall.
The temporal bone is related posteriorly with the occipital, superiorly with the parietal and
frontal, externally with the quadratus, anteriorly with the ethmoid, and inferiorly with the
sphenoid.
Description.—The temporal bones consist of the fused squamous and petrous
temporals; they contain the essential organs of hearing.

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Fig. 8.—Inferior view of the skull of a hen. 1,
Occipital. 2, Foramen magnum. 3, Occipital
condyle and just below the basi-occipital. 4,
Foramen for the passage of the hypoglossal
nerve. 5, Foramen for the passage of the vagus.
6, Canalis caroticus and jugulare. 7, Sphenoid.
8, Temporal wings of the sphenoid. 9, Foramen
auditiva. 10, Os articulare. 11, Os angulare. 12,
Vomer. 13, Os dentale. 14, Pterygoid.

The squamous portion of the temporal bone possesses the long thin zygomatic process
sometimes called the posterior orbitalis. It forms a small flattened tongue, directed
forward, sometimes free, and at other times united by its superior border to the summit of
the orbital process. This is especially true in the turkey. This process is seen near the lower
outer portion of the posterior orbital wall. The squamous portion is also provided antero-
laterally with an articular facet which articulates with the quadrate bone. The large portion
of the temporal bone lies on the side of the cranium superior to the ala sphenoida
temporale. It extends outward and anteriorly over the rims of the petrosum and ala
sphenoida orbitale. The squamous part forms the upper three-fourths of the cochlea, the
inner auditory canal, the upper part of the fenestra ovalis, the anterior vertical and the
outer semicircular canal, and the lower part of the posterior vertical semicircular canal.
The petrous portion forms the posterior wall of the foramen ovale and the fenestra
ovalis in which lies the columella. The fenestra ovalis and the fenestra rotunda are the
only two entrances into the labyrinth. In this region may be seen the fusion line between
the os petrosum and the os occipitale. Superiorly and posteriorly the petrous portion
touches the external parietalia and occipitalis; infero-laterally it unites with the basi-

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sphenoid. The outer rim of the foramen ovale is broadened by the ala sphenoida and
mesially by the basi-sphenoid. This foramen gives exit to the second and third divisions of
the fifth pair of cranial nerves.
The lateral surface of the temporal bone presents a short tube, the external acoustic
process, or processus acusticus externus, to which is attached the concha of the ear. The
process is directed outward. Its lumen, the external acoustic meatus, or meatus acusticus
externus, conducts to the cavity of the middle ear in the bare skull, but is separated from it
by the tympanic membrane in the natural state.

Bones of the Face

The bones of the face, or ossa faciei, are the premaxillary, or upper mandible, the
maxillæ, the nasal, the lacrimal, the palatine, the pterygoid, the zygomatic, the vomeral,
the jugal and the quadrato-jugal. The vomer is single, the others are paired. In the inferior
maxillary group there are the quadrati, and the inferior maxillary, or lower mandible. The
turbinated and hyoid bones are also discussed with the bones of the face.
The beak consists of the anterior portion of the upper and lower mandibles which are
covered with a horny structure.

The Premaxilla. Location.—The premaxillæ, or ossa incisiva, or mandibular
structures, are located in the extreme anterior facial region.
Description.—The premaxillæ are long and the anterior end is pointed. Each consist of
two lateral halves which become fused before the chick is hatched. They partly
circumscribe the openings into the nose. This bone is the base of the upper portion of the
beak and determines its form. It forms the anterior walls of the nasal cavity. It has between
the nasal bones, two processes which extend back to the anterior point of the cerebral
cavity. The posterior part of the incisivum and nasale are flat, thin, and elastic. The
extensions then are the processus maxillaris, the processus palatinus, and the processus
frontalis, the first of which forms part of the jaw rim, the second, which aids in forming
the gum plate, and the last which reaches to the anterior portion of the cranial wall.

The Maxilla. Location.—The superior maxillaries, or ossa maxillares, two in number,
form the floor of the upper beak, a part of the palatine roof and nasal walls.
Each maxilla borders laterally the premaxilla and the nasal; inferiorly, the anterior point
of the palatine; and posteriorly, the jugale.
Description.—The maxillæ are thin, flat, bones. They have three borders and three
angles. The palatine processes of the two bones do not meet in the median line, which
results in a cleft in the median palatine region. The bone-like gums are formed partly by
the palatine processes but more largely by lateral wings of the os incisivum. Each maxilla
has posteriorly a yoke-like extension, superiorly a small extension, and also a palatine
process. The latter articulates by a facet with the vomer.

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The Nasal. Location.—The nasal bones, or ossa nasalia, two in number, are located in
the lateral facial region. The nasal bone articulates posteriorly with the frontal; laterally,
on the inner border, with the processus frontalis of the premaxilla, and on the outer border
with the lacrimal; and inferiorly with the premaxilla, maxilla, jugale, and vomer.
Description.—The nasal bone, or os nasale, is broad, flat, and elastic and forms the
posterior wall of the nasal opening. Under this bone is located the infraorbital sinus.
There are three extensions: first, the processus intermaxillaris, which forms the upper
wall of the nasal cavity; second, the processus maxillaris anterior, directed downward and
forward, which fuses with the maxillary bone and forms the posterior rim of the nasal
cavity; and third, a posterior processus frontalis, which lies parallel with the ethmoid.

The Lacrimal. Location.—The lacrimal bones, or ossa lacrimalia, two in number, are
located at the outer border and at the junction of the processus frontalis of the nasal, with
the frontal bone.
Description.—The lacrimal bone is small, and rather filiform. They become fused with
the nasal and the frontal bones, forming part of the margin of each.

The Palatine.—Location. The palatine bones, or ossa palatina, two in number, enter
into the formation of the inner part of the bony gum and hard palate, or roof of the mouth.
They form the support for the hard palate. Each palatine articulates posteriorly with the
rostrum, or nasal portion of the sphenoid, and with the pterygoid; and anteriorly with the
maxilla.
Description.—The palatine bone is curled posteriorly and is thin at the upper portion
and thick at the lower border. Anteriorly it has a long rather filiform projection.

The Pterygoid. Location.—The pterygoid bones, or ossa pterygoidea, two in number,
are located back of the region of the posterior nares. They extend diagonally outward and
backward from the median region of the sphenoid rostrum to the quadrate bone. They
articulate anteriorly with the sphenoid rostrum and the palatine, and posteriorly with the
quadrate.
Description.—The pterygoid bones are slender and cylindrical, and are expanded at the
ends into an articular facet.

The Zygomatic. Location.—The zygomatic, or ossa zygomatica, two in number are
situated below the orbital cavity and extend from the maxilla to the quadrate bone.
Description.—The zygomatic is small, slender, rod-shaped, and forms the lateral
portion of the upper jaw. The anterior portion of the zygomatic represents the jugal and is
fused with the maxilla and with the anterior processus maxillaris of the nasal bone, the
maxilla, and the posterior portion, the quadrato-jugal, which articulates with the quadrate
bone.

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The Vomer. Location.—The vomer is located in the median nasal septum. It articulates
with the rostrum of the sphenoid, being connected to it by a mass of ligaments. It touches
anteriorly the posterior portion of the maxilla.
Description.—The vomer is a median bone and aids in the formation of the septum
nasi. It consists of a thin plate, thickest posteriorly and diminishing toward the anterior
edge.

The Jugal and Quadrato-jugal.—The jugal and quadrato-jugal are united forming a
long slender cylindrical bone called the zygomatic, lying at the outer side of the upper jaw.
They have been described under zygomatic, which see.

The Quadrate. Location.—The quadrate bones, or ossa quadrata, two in number, are
located antero-laterally to the temporal bones. Each articulates inferiorly with the posterior
articular portion, or pars articulare, of the inferior maxilla and infero-laterally with the
quadrato-jugalare portion of the zygomatic. It articulates antero-internally with the
pterygoid and supero-posteriorly with the temporal.
Description.—The quadrate bone is anvil-like in shape. It has an anterior process, the
orbital process, for muscular attachments, and posteriorly it affords attachment to the ear
drum.

The Inferior Maxilla. Location.—The inferior maxilla, lower jaw, or os maxillare
inferius, also called the mandibular bone, or pars dentis, is analogous to the lower jaw of
mammals. It articulates posteriorly with the quadrate bone.
Description.—The inferior maxilla is the largest bone of the face. It is made up of a
right and a left limb which are separate in the fetus and which unite subsequently
anteriorly, forming the inferior portion of the beak. Each limb of the jaw is developed
from five elements: the pars articularis, which forms the jaw-joint and, expanded,
articulates with the quadrate bone; the pars angularis, lying just in front of the pars
articularis; the pars supra-angularis, a slender bone lying just above the angularis; the
splenial, a thin plate of bone, lying along the inner surface of the mandible; and the pars
dentalis, which forms the anterior portion of the jaw.

The Turbinate Bones. Location.—The turbinate bones, or ossa turbinata, six in
number, are attached to the lateral walls of the nasal cavity (Fig. 26, No. A, 1 and 2). In
each nasal cavity there are three turbinate bones, one anterior and two posterior. Of the
two posterior the upper one lies supero-posterior to the inferior one. The turbinate bones
are attached to the lateral nasal walls, project into the cavity and thus greatly diminishing
its extent.
Description.—Each turbinate bone is composed of a very thin lamina, finely cribriform
in many places, and in the fresh state, covered on both sides with mucous membrane.

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These bones are curled and partly membrano-cartilaginous structures which give greater
surface in the nasal passage for mucous membrane in which the olfactory nerve terminal
filaments are distributed.

The Nasal Cavity.—The nasal cavity, or cavum nasi, is a longitudinal passage which
extends through the upper part of the face. It is divided into right and left halves by a
median septum nasi. Its walls are made up of the premaxilla, maxilla, nasal, vomer, and
palatine bones.

The Hyoid Bone. Location.—The hyoid bone, or os hyoideum, is situated chiefly
between the rami of the mandible, but its upper part extends around the outer margin of
the base of the skull. The hyoid bone does not articulate with any bones of the skull, but is
firmly attached by strong fibrous structure.
Description.—The hyoid bone consists of the following parts: the body, or basi-hyal,
which is subcylindrical and presents in front a trochlear articular surface, convex
transversely, and concave vertically for articulation with the ewer-shaped portion of the
glosso-hyal. The anterior free portion, or lingual process, is called the glosso-hyal, or
entoglossal bone. The lingual process gives support to the muscular and fibrous structures
of the tongue. On either side of the basi-hyal there is a limb passing posteriorly along the
side of the superior larynx, extending upward along the outer border of the occipital bone.
This is the cornu of the os hyoideum and is divided into two elements, first, the basi-
branchial which is bone and articulates with the basi-hyal, and the second, the cerato-
branchial, cartilaginous in structure. In the center and projecting backward from the body
of the os hyoideum is a spur process called the uro-hyal, partly bony and partly
cartilaginous, and which rests upon the superior larynx.

THE VERTEBRAL COLUMN

The vertebral, or spinal column consists of 42 bones, as shown in the following table:

Cervical region 14
Dorsal region 7
Lumbo-sacral region 14
Coccygeal region 7

Total 42

Many of the bones of the dorsal and lumbo-sacral regions do not have free articulations.
The cervical and coccygeal alone have free movements.

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The Cervical Vertebræ (Fig. 4, No. 59; Fig. 5, Part II, No. 2). Location.—The cervical
vertebræ form the neck of the fowl.

Fig. 9.—Os hyoidum and tongue muscles. 1,
Glosso-hyal. 3, Basi-hyal. 4, Basi-branchial
element of the cornua. 5, Cerato-branchial
element of the cornua. 6, Uro-hyal or spur
process. 7, Genio-hyoideus. 8, Cerato-hyoideus
showing the slender tendon. 9, Hyoideus
transversus. 10, Hyoideus transversus.

Description.—The long cervical section of the spinal column is S-shaped and is made
up of fourteen vertebræ. The anterior segments move freely forward, the middle ones
backward and the posterior ones forward, allowing the S-shaped curve of the neck. The
neck is flexible so that it is possible for the beak to reach the coccygeal oil gland. The bird
is enabled to reach the feathers on all parts of the body to cleanse and oil them.

The Atlas. Location.—The first cervical vertebra is called the atlas. Anteriorly it
articulates with the single condyle of the occipital bone. Posteriorly it articulates with the
axis, or second cervical vertebra.
Description.—The atlas is the smallest of the cervical vertebræ and is ring-shaped. The
anterior articular surface, half-moon in shape, forms a deep articular cavity. The joint,
called a ball-and-socket joint, makes possible movements in all directions. The condyle of
the occiput also touches an articular end of the odontoid process of the axis, or second

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cervical vertebra. Posteriorly there projects from the atlas two small lateral wings
possessing articular facets which articulate with similar facets on the lateral wings of the
axis. Posteriorly the body of the atlas is also provided with an articular surface which
articulates with a similar surface on the anterior portion of the body of the axis.

The Axis. Location.—The axis is the second cervical vertebra. It articulates anteriorly
with the atlas, and by a facet on the extreme anterior end of the odontoid process, with the
condyle of the occipital bone. Posteriorly it articulates with the third cervical vertebra.
Description.—The body of the axis is short. The upper anterior portion of the body of
the axis is provided with a tooth-like process called the odontoid process. There are two
anterior lateral wings provided with small articular facets which articulate with similar
facets of the atlas. The anterior surface of the body of the axis forms a true articulation
with the body of the atlas.
The axis is provided with a superior and an inferior spine. There are two posterior
articular processes which articulate with the prezygapophyses, or anterior articular
processes, of the third cervical vertebra. The posterior part of the body of the axis forms a
true articulation with the body of the third cervical vertebra.

Other Cervical Vertebræ.—Beginning with the axis, the body of which is relatively
short, the body of each succeeding vertebra is longer than that of the preceding. The
articulations of each vertebra with adjoining vertebræ are effected by means of
diarthrodial facets, convex in one direction and concave in the other.

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Fig. 10.—A. Diagram of three first dorsal
vertebræ and scapular arch-side view. B.
Diagram of section through the hemal arch.

A. 1, First dorsal segment. 2, Second. 3, Third. 4
and 5, Hemal arches. 6, The pleurapophyses or
floating ribs. 7, The third pleurapophyses or
dorsal vertebral rib articulating with the
hemapophysis or sternal rib, 8, and this in turn
with the wing of the sternum form a hemal arch.
9, The sternum. 10, Intervertebral foramen
through which the nerves pass. 11, Articulation
with the body of vertebra parapophyses. 12,
Articulation with transverse process or
diapophyses. 13, Oblique process or
zygapophysis. 14, The epipleural appendage.

B. 1, Hemal or inferior spine (hypapophysis). 2,
The neural arch. 3, The pleurapophyses or rib.
4, The superior or neural spine or neurapophysis
which aids in the formation of the anapophyseal
ridge. 5, Parapophyseal surface for head of rib.
6, Tubercle of rib articulating with the
diapophysis. 7, Lamina of neurapophysis. 8,
Centrum. 9, Hemal arch.

Between the bodies of the vertebræ are pads of fibrous cartilage. Above these bodies
and inferior to the neural spines extends throughout the spinal column the large neural
canal which is occupied by the spinal cord. Between the vertebral segments the neural

Page 38

canal is exposed superiorly, since here the neural arches do not completely bridge the
canal. These spaces are protected by intervertebral ligaments.
In addition to the superior neural spines and the inferior spines, from the body of the
vertebra project lateral processes, and anterior and posterior oblique processes.
All cervical vertebræ except the atlas and the axis are made up of the following parts: a
body, or centrum, a neural canal, a neural arch, a superior dorsal, or neural spine, or
neurapophysis, which in most cervical vertebræ is only slightly developed, two oblique
processes, or zygapophyses, two transverse processes, or diapophyses (Fig. 10, No. 12)
and in some vertebræ two tubercles, or anapophyses above the posterior zygapophyses.
The prezygapophyses are directed upward and inward; the postzygapophyses are directed
downward and outward. The inferior spines are only well developed in the last two or
three cervical vertebræ.
Between vertebral segments, except the central sacral portion, on each side, there is an
intervertebral foramen (Fig. 11, No. A, 4), through which pass the spinal nerves. In the
central portion of the sacrum where the vertebræ have fused, there are two foramina on
each side for each original vertebra, one located above the other, the upper giving passage
to the sensory branch, the lower to the motor branch of the nerve.
The Dorsal Vertebræ (Fig. 4, No. 23; Fig. 11, A). Location.—The dorsal, or thoracic
vertebræ, or vertebræ thoracicales, aid in forming the roof of the chest cavity.
Description.—The dorsal vertebral section is made up of seven vertebræ, with strong
short bodies. The first and sixth dorsal segments articulate as do the cervical, by the bodies
and oblique processes. (Fig. 11, No. A, 3, illustrates the oblique processes.) The seventh
dorsal is fused with the first lumbo-sacral vertebra. The second to the fifth inclusive of the
vertebræ are fused together, and the superior and inferior spinous processes are fused into
a prominent plate-like ridge.
The transverse processes of the dorsal vertebræ, from the second to the sixth, are well
developed and are bridged over with a thin layer of bone. The ventral spines are partly
fused and form a very prominent and continuous ridge. (Fig. 11, No. A, 1, shows the fused
superior spines; No. 2, the fused inferior spines; and No. 4, the intervertebral foramina.)
The Lumbo-sacral Vertebræ (Fig. 5, Part II, No. 4). Location.—The fused lumbo-
sacral section of the spinal column forms the roof of the pelvic cavity.

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Fig. 11.—Bones from the scapular arch.

A. Dorsal vertebra. 1, Superior spinous ridge, 2,
Inferior spinous ridge. 3, Oblique processes. 4,
Intervertebral foramina. 5, Articular facette for
head of the rib. 6, Articular facette for tubercle
of the rib. 7, Articular portion of the body.

B. Outer surface of scapula.

C. Inner surface of scapula. 1, Thin caudal end.
2, Articular head. 4, Processus furcularis. 5,
Processus humeralis. 6, Processus coracoideus.

D. Outer surface of coracoid.

E. Inner surface of coracoid. 1, The furcular
tuberosity. 2, Articular facette for articulation
with the sternum. 3, Articular surface for
humerus and scapula.

F. Outer surface of humerus and G the inner
surface of the same. 1, Trochanteric fossa. 2,
Oval articular head at proximal end. 3, Shaft. 4,
Distal end showing articular condyles. 5,
Trochanter. 6, Trochlea for ulna. 7, Trochlea for
radius. 8, Depression or fossa.

H. Section through the median plane of the
humerus showing the delicate cross partitions
illustrating provisions made for bones provided
with air-sac extensions.

Page 40

Description.—The lumbo-sacral region consists of fourteen vertebræ which are distinct
in the body of the newly hatched chick, but which become fused soon after hatching. With
these vertebral segments there are fused the last dorsal and first coccygeal vertebral
segments. This fusion is so complete that the segments are indicated only by the
intervertebral foramina on the sides through which the spinal nerves pass, and by
transverse markings on the inferior surface of the bodies.
The lumbo-sacral vertebræ, called the sacrum, and the ilia are fused. The dorsal spines
of the vertebral segments are indicated only in the anterior portion where they are fused,
forming a plate. There are no prominent ventral spines.
The Coccygeal Vertebræ (Fig. 4, No. 27). Location.—The coccygeal or caudal
vertebræ, or vertebræ coccygeæ, constitute the bones of the tail.
Description.—There are seven coccygeal vertebræ. The last segment, shaped like a
plough share and therefore called the pygostyle, is the largest and is supposed to have
been formed by the fusion of several original distinct segments. It supports the coccygeal
oil gland and the row of rudder feathers, or rectrices, which are arranged fan-wise.
All of the coccygeal vertebræ except the first are freely movable, thus allowing the tail
to be used as a rudder during flight. The lateral spines are long and well developed, and
the superior spines are bifurcated, thus giving increased surface for muscular attachment.
The first coccygeal segment is fused with the last lumbo-sacral vertebra.

THE THORAX

The dorsal vertebræ superiorly, the ribs laterally, and the sternum, or breast-bone
inferiorly, form the skeleton of a large cavity called the thorax. The dorsal vertebræ have
been described.
The Ribs (Fig. 4, No. 32; Fig. 10, A and B). Location.—The ribs form the lateral bony
wall of the thorax, articulating superiorly with the dorsal vertebræ.
Description.—The ribs are arranged in order of length, the ultimate rib being the
longest. From anterior to posterior, they approach more nearly a horizontal position. The
ribs are divided into the true and the false. The true ribs articulate with the sternum. The
false ribs do not touch the sternum; they are floating. The true ribs are composed of two
parts, a vertebral, or dorsal, and a sternal, or ventral. The vertebral part, or extremitas
vertebralis, is provided with an articular head, or caput costæ; a neck, or collum costæ;
and an articular tubercle, or tuberculum costæ. The head and tubercle articulate with the
dorsal vertebra. Below the head of each rib is a pneumatic foramen.
The distal extremity of the dorsal section of the rib articulates with the proximal end of
the sternal section by a diarthrodial articulation.
The articulations of the true ribs with the sternum is diarthrodial and each articulate by
two small ridges with a double sternal facet. The first, the second, and the seventh ribs are
floating, or false ribs. The first rib articulates with the quadrate part of the last cervical
vertebra and also with the first dorsal vertebra. The seventh, the last rib, articulates with

Page 41

the under side of the anterior alar part of the ilium. This rib is situated similarly to the true
ribs; but, instead of articulating directly with the sternum, the lower end lies against the
sternal segment of the rib just anterior to it.
From the posterior edge of the second, the third, the fourth, and the fifth ribs, and near
the middle of the dorsal segment, are flat, uncinate, bony processes which project upward
and backward, overlying in each case, the succeeding rib and giving greater surface for
muscular attachments and greater stability to the thorax.
The Sternum (Fig. 4, No. 40; Fig. 10, No. A, 9). Location.—The sternum, or breast-
bone forms the inferior portion, or floor of the thoracic cavity.
Description.—The sternum is a quadrilateral, curved plate with processes projecting
from each angle and from the middle of the anterior and posterior borders. The posterior
medial projection, or metasternum, is the longest, and has a tall, plate-like ridge—the
sternal crest, crista sterni—running along its ventral surface. The crest serves the
important function of increasing the bony area for the attachment of the powerful muscles
which move the wings. The anterior medial projection, or rostrum, is short, and pierced at
its root by an opening from which extend two elongated, saddle-shaped depressions into
which the end of the coracoid bones are received.
The plate-like process of bone, the posterior lateral process, which projects from the
caudal angles of the sternum soon divides into two parts. The shorter of these, the oblique
process, broadens toward its free end and covers the sternal segments of the last two ribs.
The sides of the sternum are thus provided with an external and an internal process
forming an external and an internal notch. These notches are bridged over by a broad
ligament, to which the muscles are attached. In poor flyers, as the domestic fowl, these
notches are large. The posterior end of the sternum is called the xiphoid process or
processus xiphoideus. Anteriorly the sternum is provided with lateral external processes,
the costal processes. The lateral borders of the sternum are pitted by four depressions into
which the sternal segments of the ribs are received. The dorsal, or inner surface of the
bone is pierced by openings by which the air-sacs communicate with the interior.

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The Appendicular Skeleton

The appendicular skeleton consists of the shoulder girdle, the fore limb, the pelvic
girdle, or hip bone, and the hind limb. The shoulder girdle consists of the scapula, the
coracoid, and the clavicle. The fore limb consists of the arm, forearm, and the hand. The
arm consists of the humerus, the forearm of the radius and the ulna; and the hand consists
of the carpus, the metacarpus, and the phalanges. The pelvic girdle consists of the ilium,
the ischium, and the pubis. The hind limb consists of the thigh, the leg, and the foot. The
thigh consists of the femur, and the leg consists of the tibia and the fibula. The foot
consists of the metatarsus and the phalanges.

THE SHOULDER GIRDLE

The shoulder girdle consists of the scapula, the clavicle and the coracoid.
The Scapula. Location.—The scapula (Fig. 11, A, B) lies on the outer and superior rib
surface, extending parallel with the dorsal vertebræ.
Description.—The scapula is a thin, sword-like bone, becoming thicker as it approaches
the shoulder-joint. The scapula expands and becomes thin near the free end, which reaches
nearly to the antero-lateral portion of the ilium (Fig. 4, No. 24). The scapula articulates
with the coracoid. A pneumatic foramen is located at the base of the acromion process.
The anterior part of the scapula is provided with an articular head and is provided with an
inner process, called the processus furcularis, which lies near the furcula and coracoid. An
outer stronger processus humeralis forms the posterior half of the glenoid cavity, or
cavitas glenoidalis, in which the humerus articulates and the processus coracoideus.
The Clavicle. Location.—The clavicles, commonly known as the wish bone, are
located in the anterior chest region.
Description.—The clavicles are long, slender bones uniting below in the hypocledium, a
laterally flattened process. They are joined to the upper end of the coracoid by fibrous
cartilage. The hypocledium is joined to the anterior point of the sternum by the
claviculosternal ligament. The clavicles, as united by the hypocledium, form a v-shaped
structure called the furculum, or, popularly, the wish bone.
The forks play the part of an elastic spring, whose office it is to prevent the wings from
coming toward each other during contraction of the depressor muscles. The conformation
of this bone is, therefore, like the sternum, related to the extent and power of flight; and
for this reason it is that, in swift flyers, the two branches of the furculum are thick, solid,
widely separated, and curved like a U; while in those that fly heavily and with difficulty,
these branches are thin and weak, and join at an acute angle. The latter formation greatly
diminishes its strength, and lessens, in a singular manner, the reactionary power of the
bony arch it represents.

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The Coracoid. Location.—The coracoid is located just back of the clavicle and at the
side of the entrance of the thoracic cavity. It is the strongest bone of the shoulder girdle,
extending upward, outward, and forward. It articulates inferiorly with the sternum and
superiorly with the humerus and the scapula, and is attached to the superior end of the
furcular limb by a fibrous cartilage.
Description.—It is thinnest in the center or shaft and broadens toward the inferior
extremity. The upper hook-like part of the coracoid forms the fore part of the glenoid
cavity, and together with the scapula and furcula form the foramen triosseum through
which passes the tendon of the elevator muscle of the wing. The upper end flattens out
into three tuberosities, the tuberositas furcularis which is thick and to which attaches the
limb of the furcula, the tuberositas scapularis which unites to the scapula, and the
tuberositas humeralis which lies between these and articulates with the humerus.

THE FORE LIMB

The bones of the fore limb are humerus, ulna, radius, carpus, metacarpus, and
phalanges.
The Humerus. Location.—The humerus constitutes the arm, which, when at rest, lies
parallel to the dorsal vertebræ. It articulates superiorly with the glenoid cavity, a shallow
ball-and-socket joint, formed by the scapula and the coracoid; and inferiorly with the ulna
and radius.
Description.—The proximal extremity of the humerus is provided with a trochanter
(Fig. 11, G, No. 5) and a large oval head or caput humeri, which articulates in the glenoid
cavity. The head is an elongate, semi-oval convexity, with the long axis transverse from
the radial to the ulnar side and with the ends continued into upper and lower crests. The
upper crest of the head of the humerus is on the radial side and the lower crest on the
under side. Under this latter crest there is a pneumatic fossa (Fig. 11, F, No. 1), at the
upper end of which there is an opening into the bone, the pneumatic foramen, which
brings the air-sac into communication with the air space of the bone. The shaft, or corpus
humeris, is irregularly cylindrical and slightly S-shaped.
The proximal part of the shaft, which is expanded on the palmar side, is concave across
and convex lengthwise. The distal part is slightly flattened. The shaft of the humerus is
almost cylindrical.
The distal extremity of the humerus is provided with two articular condyles, one of
which articulates with the ulna and the other with the radius. On the radial side of the
palmar surface there is a ridge; and on the ulnar side of the same surface there is a second
ridge diverging to the opposite tuberosity. The radial surface is a narrow, subelongate
convexity, extending from the middle, approximately, of the palmar surface, obliquely to
the lower part of the radial tuberosity. The two articular convexities, or trochlea, at the
distal end of the humerus are bent toward the palmar aspect, the anconal aspect is the side
on which the elbow is situated. The inner convexity is the larger and articulates with the
ulna. To the outside is the processus cubitalis humeri. The outer articulates with the radius

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and is so arranged that the radius makes a greater flexion than the ulna. At the lower end
of the humerus there is a depression which receives the anconeus of the ulna during
flexion and extension of the forearm. On the shoulder- and elbow-joint are found grooves
over which the tendons glide, at which places sheaths are provided. This arrangement also
aids in keeping the capsular ligament in place.
The Ulna. Location.—The ulna, larger than the radius, is bent and articulates with the
radius only at the ends. The two bones are bound together by a ligamentous band. It also
articulates superiorly with the distal end of the humerus, and inferiorly with the carpus.
When the wing is folded the radius is superior and a trifle to the inner side of the ulna.
Description.—The proximal end is most expanded, and is obliquely truncate for the
articular excavation adapted to the ulnar tubercle of the humerus. A short angular process
behind the cavity represents the olecranon, which is the processus olecranalis
coracoideus ulnæ to which the ligamentum capsulare cubiti attaches. On the inner side of
the head is the internal tubercle of the ulna and on the external side the external tubercle of
the ulna. An excavation is noted on the radial side of the proximal end for the lateral
articulation of the head of the radius. On the upper side near the articular part is located
the sigmoid cavity.
The shaft, or corpus ulnæ, decreases in size near the distal end. It is slightly curved,
flattened laterally with an internal and an external ridge.
The distal end of the ulna is slightly expanded into a trochlea which is sharply convex
and articulates with two free carpal bones, the scapho-lunar, or os carpi radiale, and the
cuneiform, or os carpi ulnare. The scapho-lunar is placed on the radial side, and the
carpiulnare on the ulnar side. The distal extremity of the ulna is provided with a styloid
process and on the dorsal side with a tubercle.
The Radius. Location.—The radius lies beside the ulna with which it articulates at each
extremity. At the inferior extremity the articulation is rotary. It also articulates superiorly
with the humerus and inferiorly with the os carpi radiale.
Description.—The radius, cylindrical in shape, is more slender than the ulna.
The proximal end is expanded, subelliptical, with a concavity for the oblique tubercle
and a thickened convex border for articulation with the ulna. This end is provided with the
tuberositas radii.
The shaft, or corpus radii, is slender, subcompressed, and has a slight bend upward from
the ulna. A nutrient foramen occurs in this shaft.
The distal end is expanded and rather flattened with two grooves on the anconal side for
passage of tendons. For articulation with the scapho-lunar the radius is provided with a
terminal transverse convexity produced palmad, which also articulates with the ulna
laterally. There is a tuberosity on the radial side of the expansion and inferiorly the
inferior tuberculum ossis carpi radialis and superiorly a superior tuberculum ossis carpi
radialis.
The Hand.—The hand is made up of the carpus, the metacarpus, and the phalanges.
The bones of the hand are so arranged as to allow abduction and adduction, or flexion
in the ulno-radial plane, movements which are necessary in the outspreading and folding

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of the wing. Thus the hand of the fowl moves in a state of pronation, without the power of
rotation. The carpal bones are so placed between the anterior arm and metacarpus as to
reduce the abduction which is necessary to hold and extend the wing, so that the hand or
wing be in a fixed position.
The Carpus.—The carpus in the domestic fowl is represented by two bones, ossa carpi,
called the scapho-lunar, or os carpi radiale, and the cuneiform, or os carpi ulnare. The
scapho-lunar is the smaller and is located between the radius and metacarpus. The
cuneiform is the larger and is located between the ulna, the radius, and the metacarpus.
The cuneiform is somewhat anvil-like in shape, being provided with a body and two
prongs.
The Metacarpus.—The metacarpal bones, or ossa metacarpi, two in number, are
separated at their middle portion, and consolidated at their extremities. The upper
proximal base of the metacarpus is provided with a tubercle, the tuberculum muscularis,
and externally the tuberculum ulnare ossis metacarpi. The distal end of the metacarpal
bone is provided with a tuberculum articulare.
The Phalanges.—The first three fingers only are represented, and these are
rudimentary.
The first finger called the pollex or thumb, consists of but one joint. It is located on the
proximal and outer end of the metacarpal bone. It has on its proximal end a tubercle, the
tuberculum articulare.
The second finger, the best developed, consists of two phalanxes. These are the main
bones extending from the metacarpus. Each articular end is provided with a tuberculum
articulare.
The third finger, small, cylindrical in shape, is located at the distal and inner side of the
metacarpal bone.

THE PELVIC GIRDLE (Fig. 4, No. 25; Fig. 5, Part II, 6)
The pelvic girdle is made up of three bones as follows: the ilium, the ischium, and the
pubis, all of which are fused in adult life. They are separate in the baby chick (Fig. 5, Part
II, 6). The pelvis together with the lumbo-sacral vertebræ forms a thin, irregular, shell-like
structure extending superiorly from the tail to the thoracic region. The sacrum is broad
posteriorly and together with the ilium forms the pelvic roof. The ilium and ischium are its
lateral walls.
The top surface of the pelvis shows the fovea ilio-lumbalis dorsalis, which is bounded
mesially by the crista ilii. Between it and the spina lumbalis there is a broad furrow, the
bottom of which is formed by the dorsal surface of the lumbar vertebræ. The sulcus ilio-
lumbalis dorsalis is formed by the rims of the ilia, so that a ridge is observable. The
cavum ilio-lumbale dorsale is formed by the iliac rims on either side. Anteriorly is the
canalis ilio-lumbalis, which is formed by the ilium and the lumbar vertebral spines. It is
located longitudinally to the vertebræ. The anterior opening of this canal is the larger.
Posterior to the acetabulum is the post-acetabular ridge.

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The under part of the pelvis presents three distinct regions. The cavity is divided into
the fovea lumbalis, or anterior part, the fovea ischiadica, or mesial part, and the fovea
pudendalis, or posterior part. Posterior to these is the region called the planum coccygeum.
The fovea lumbalis contains the anterior lobe of the kidney, and is circumscribed
anteriorly by the last rib-carrying vertebra, and posteriorly by the transverse process of the
last lumbar vertebra.
In the fovea ischiadica which follows, lie the nerve plexus ischiadicus and the middle
lobe of the kidney. Its posterior boundary is the linea arcuata. The linea arcuata is a line
drawn from the acetabulum of the one side to the acetabulum of the other side.
The fovea pudendalis contains the posterior lobe of the kidney. The posterior boundary
is the anterior border of the first coccygeal vertebra. It gives passage to the nerve plexus
pudendo-hemorrhoidalis.
The ilium, the ischium, and the pubis join to form the cotyloid cavity, or acetabulum, in
which articulates the head of the femur. The floor of the cavity is perforated by a relatively
large round foramen.
The Ilium. Location.—The ilium, together with the lumbo-sacral vertebræ, forms the
roof of the pelvic cavity. It articulates at its inner border with the lumbo-sacral vertebræ,
postero-laterally with the ischium and at the cotyloid cavity with the pubis.
Description.—The ilium is remarkable for its development in the long axis of the
vertebral column. It is long and narrow; and mesially, where it is thickest it forms the
upper wall of the acetabulum. Anterior to the acetabulum it is outwardly concave, and
posterior to the acetabulum it is convex. The ilium fuses with the last dorsal vertebra and
with the lumbo-sacral vertebræ and is excavated on its internal face. This surface is
irregular and lodges the kidneys. This inner margin of the renal part enters with the square
extensions of the posterior excavation passing into the posterior iliac spine. The external
margin is the extension of the crista transversa and forms the processus ischiadicus.
Posteriorward the renal part of the ilium joins the ischium.
The ilia converge at the summits of the anterior sacral spines forming the ilio-lumbar
spines.
The ilium is joined to the square extensions of the last sacral vertebra by the symphysis
ilio-sacralis, to the larger part of the lumbar vertebræ by the sutura ilio-lumbalis, and to
the transverse processes of the last sacral vertebræ by the symphysis ilio-sacri.
The Ischium. Location.—The ischium is located in the postero-inferior part of the
pelvis. It joins superiorly with the ilium, and inferiorly with the pubis.
Description.—The ischium is smaller than the ilium and is a flattened, triangular-
shaped bone, thickest where it forms the posterior part of the acetabulum, becoming
thinner and broader as it extends backward. Posteriorly it forms the caudal extension. The
inferior border is turned slightly outward and is fused with the pubis. Between these bones
there is located the large oval ischiadic foramen, through which passes the ischiadic nerve.
This bone aids the ilium in the formation of the obturator foramen through which passes
the tendon of the internal obturator muscle. The lower part of the ischium which separates

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the ischiadic foramen from the obturator foramen is called the ramus ascendens ossis
ischii.
The Pubis. Location.—The pubis is located along the inferior margin of the ischium
and extends further back than the posterior border of the ischium.
Description.—The pubis is a long, slender, rib-like bone. It forms the lower and front
portion of the acetabulum. The ischiadic foramen formed by the ischium and pubis is
single and nearly circular in fowls, double in pigeons, and in geese and ducks it is
elongate.

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THE HIND LIMB (Fig. 4, Nos. 35, 47, 48, 49, 50, 51, 52, and 53; Fig. 12)

The pelvic, or hind, limb supports the body. The bones of each leg are the femur, which
constitutes the thigh, the tibia and the fibula, which represents the leg, and the metatarsus
and the phalanges, which form the foot.
The Femur (Fig. 12, A and B). Location.—The femur, or os femoris, the first bone of
the hind extremity, extends obliquely downward and forward, articulating with the
acetabulum above and the tibia, the fibula, and the patella below.
Description.—The femur, one of the largest, thickest, and strongest bones of the body,
belongs to the class of cylindrical bones, and presents for examination a shaft and two
extremities.
The superior, or proximal extremity, is provided with a head, caput femoris; the neck,
collum femoris; and the trochanter. The head is relatively small, and is marked by a
depression above for the round ligament which fills the cavity in the acetabular wall. Its
axis is nearly at right angles with the shaft. A neck joins it to the body at the proximal end.
External to the head of the femur is the trochanter. The trochanter presents an outer
convexity over which the tendon of the gluteus maximus extends to become inserted
below. The trochanteric ridge, which is opposite the articular head, presents an outer
flattened surface which possesses impressions for muscular attachments. The trochanteric
fossa, or fossa trochanterica, is shallow.
The shaft, or corpus femoris, is shorter than the tibia, is in general cylindrical, bent
forward, and the lower half is flattened and expanded transversely. A nutrient foramen is
located in the median portion of the shaft. The shaft shows muscular linear ridges.
The distal extremity is large in both directions and comprises the trochlea in front and
two condyles behind, one internal and one external. The condyles are separated by the
intercondyloid fossa, or fossa intercondyloidea, which is marked with pits for the
attachment of ligaments; and above this is the epitrochlear fossa.

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Fig. 12.—Bones of the hind extremity.

A. Posterior view of femur.

B. Anterior view. 1, Shaft. 2, Proximal
extremity. 3, Distal extremity. 4, Articular head.
5, Trochanter major. 6, Shallow trochanteric
fossa. 7, Convexity over which the tendon of
the gluteus maximus glides. 8, External
condyle. 9, Internal condyle. 10, Nutrient
foramen. 11, Intercondyloid fossa. 12, Muscular
linear ridges. 13, Epitrochlear fossa.

C. Internal view of tibia.

D. External view. 1, Shaft. 2, Articular head. 3,
Distal end. 4, The rotular process. 5, The fibular
ridge. 6, External condyle. 7, Internal condyle.
8, Intercondyloid space. 9, Nutrient foramen.

E. Fibula, lateral view. 1, Articular head. 2, Its
attenuated portion.

F. Posterior view of metatarsus. 1, Trochlea for
inner or second digit. 2, Trochlea for middle or
third toe. 3, Trochlea for outer digit. 4, Bony
core for spur. 5, Bony canal for tendons. 6,
Groove for tendons. 7, Fossa intercondyloidea.

The inner condyle begins anteriorly as a ridge, and expands into a convexity which
attains its greatest breadth posteriorly where it becomes more flattened. The inner side of
the inner condyle is flattened and is provided with a tuberosity at its mid-part and a second
just above the posterior part of the condyle.
The outer condyle is formed in the same manner as the inner condyle. It is indented at
its broad, lower end by an angular groove, which, winding divides the posterior part of the
condyle into two convexities. The more external convex ridge and the groove dividing it
from the outer condyle are adapted to the head of the fibula. There is in this part a fibular
ridge and above this ridge a tuberosity.

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The Tibia. Location.—The tibia (Fig. 12, D and C) extends obliquely downward and
backward from the knee-joint to the hock. It articulates above with the femur and, by its
procnemial process with the patella, below with the metatarsus, and laterally with the
fibula.
Description.—The tibia is the longest bone in the posterior limb, and possesses a shaft
and two extremities. It is largest at the proximal end and presents three faces.
The proximal extremity presents a semi-oval articular surface, not quite at right angles
with the shaft, which articulates with the condyles of the femur. The margin is raised
toward the anterior of the bone. The head of the tibia, or caput tibiæ, extends into a rotular
process which extends transversely, and is truncate. From the anterior of this process there
descends two vertical ridges; one near the angle of the rotular process, the procnemial
ridge; the other from the outer fibular angle, the ectocnemial ridge. On the outer side of
the intercondylar tuberosity there is a surface for the ligamentous union with the head of
the fibula; and a short distance below this there is a vertical ridge for the close attachment,
almost a fusion, with the fibula, called the fibular ridge.
The shaft, or corpus tibiæ is straight and the upper two-thirds subtrihedral; the lower
third oval. A nutrient foramen occurs near the upper postero-internal portion of the middle
third of the bone.
The distal extremity is much smaller than the proximal one; it is quadrangular in form.
The expanded inferior end of the tibia forms two articular condyles above which
posteriorly there is the epicondyloid fossa. The inner condyle, the larger, has a groove near
the lower end of the anterior part of the shaft, which deepens toward the intercondyloid
space. This intercondyloid fossa in young birds is covered by a strong ligament, which in
older birds, becomes ossified. On the lateral side of each condyle, there is a depression for
the attachment of ligaments.
The Patella. Location.—The patella, or knee-cap, thin and wide, articulates with the
procnemial process of the tibia, and with the deep trochlea of the distal end of the femur.
Description.—The patella is irregular in shape with three faces and three borders. The
posterior surface is articular. The other two surfaces are rough for tendinous attachment.
The patellar ligaments in old birds may become ossified.
In order to turn the foot in and out, the tibia not only turns around the inner condyle of
the femur, but also around the patella, so that the posterior surface turns outward and thus
turns outward the metatarsus and all the toes.
The Fibula. Location.—The fibula lies at the outer border of the tibia. It articulates
superiorly with the outer condyle of the femur, and laterally with the tibia.
Description.—The fibula is rudimentary; it is largest superiorly and tapers to a slender
point. The head is compressed laterally, and furnishes an upper and an inner articular
surface.
The Tarsus.—There exist, during fetal development of the chick, two rows of tarsal
bones which later become fused. The upper row fuses with the tibia and the lower with the
metatarsus. Therefore, in the adult, there is no tarsus.

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The Metatarsus. Location.—The metatarsal bone extends downward and forward. In
birds it consists of one bone, which articulates superiorly with the inferior extremity of the
tibia. On the distal end it has a threefold trochlear arrangement which articulates with the
three principal digits.
Description.—The proximal extremity posteriorly has a process which may be
considered as a consolidation of originally separate metatarsal bones. The process at the
supero-posterior part of the metatarsus is called the hypotarsus of the tarso-metatarsus,
through which extends a canal called the hypotarsal canal, and which gives passage to
flexor tendons.
The proximal end of the metatarsus is ossified from one center of ossification forming
an epiphysis which caps the ends of the three original metatarsal bones that coalesce, first
with one another, then with the epiphysis, thus forming a single compound bone. Above
and just to the inside of the metatarsus there may occur a small bone which is imbedded in
ligaments and articulates with the inner proximal surface of the metatarsus. This has been
called by Gadow a sesamoid bone.
The shaft shows tendonal grooves which are best marked on the posterior surface. The
shaft is rounded at the sides and flattened on the anterior and posterior surfaces. At the
juncture of the middle and inferior thirds of the metatarsus there is a conical process
turned slightly backward, which serves as a base for the spur. The spur is a horny
structure.
At the distal extremity occurs the threefold trochlear arrangement mentioned above,
which incloses the fossa intercondyloidea. The inner trochlea is the broadest, and the outer
the narrowest. The inner trochlea articulates with the proximal end of the second, the
middle with the third, and the outer with the fourth toe.
The Phalanges. Location.—Most domestic fowls are provided with four digits, or toes;
the Houdan and Dorking are provided with five. In fowls with four toes the three principal
toes, the second, the third, and the fourth, are directed forward, and the first, or hallux, is
directed backward.
Description.—The last phalanx of each toe, called the ungual phalanx, is slightly
curved downward, is pointed anteriorly, like the claw of the cat or dog, and is covered
with a horny sheath. The articular ends of the joints of the phalanges are enlarged. The
base of the basal phalanx has two enlargements, the superior-inferior tubercles, or
tuberculum superius et inferius, between which is located the fossa articularis transversa.
Laterally the head has two condyles, condyli laterales, which are divided by the sulcus
longitudinalis. The bodies of the phalanges vary in form; they are superiorly rounded, but
inferiorly rounded, flat, or even somewhat concave. The distal extremity has an articular
trochlea.
The first toe, or digit, called the great toe, or hallux, is composed of three phalanges, or
segments. The first segment, or basal phalanx is considered a rudimentary metacarpal
bone; it is attached by a fibrous cartilaginous tissue to the inner posterior surface of the
inferior extremity of the metacarpal bone just below the spur.

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The second toe, likewise composed of three phalanges, is directed forward. It articulates
with the inner trochlea located on the inferior metacarpal bone.
The third toe, made up of four phalanges, is the middle of the three forward toes. It
articulates with the middle trochlea of the inferior extremity of the metacarpal bone.
The fourth toe, is composed of five phalanges; it is, however, of approximately the
same length as the third, the segments being shorter. The fourth or outer toe articulates
with the outer trochlea of the distal extremity of the metacarpal bone.

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ARTHROLOGY

Kinds of Joints.—Joints may be movable, immovable, or mixed. In
movable, or true joints the articular surface of each bone is covered by
cartilage. The bones are held together by ligaments, the capsular one often
surrounding the joint and enclosing the synovial membrane. In some joints
there is a pad of fibrous cartilage interposed between the two articular
cartilages. Such a pad, called a meniscus, adds to the elasticity and the free
movement of the joint. Movable joints form the most numerous class; they
are for the most part found in the limbs.
In an immovable joint there is only a thin layer of fibrous or cartilaginous
material interposed between the bones. The fibrous layer of the periosteum
of both bones unite to cover the connecting material and becomes attached
to the same, thus serving as a ligament. If the connecting material is fibrous,
the joint is called a suture; if cartilaginous, a synchondrosis. These joints are
found in the skull and in the pelvis.
The term mixed is used with reference, not to the motion in joints, but to
their structure, which partakes of the nature of both the movable and
immovable. The bones are firmly joined by a strong interposed pad of
fibrous cartilage to which also is adherent the ligaments of the joint. There
are no capsular ligaments; the cartilaginous pad or disc is softer toward its
center, where occasionally there may be one, or even two, narrow cavities.
Authorities differ as to whether such cavities are lined by synovial
membrane or not. Since there are really no frictional surfaces in such a
joint, motion depends upon the flexibility of the disc. The joints between
the vertebral centra afford the best illustration of the mixed class.
Movement of Joints.—The movements admissible in joints may be
divided into four kinds: gliding, angular movement, circumduction, and
rotation. These movements are often, however, more or less combined in

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the various joints. It is seldom that there occurs only one kind of motion in
any particular joint.
Gliding movement is the most simple kind of motion that can take place
in a joint, one surface gliding or moving over another without any angular
or rotary movement.
Angular movement occurs only between the long bones. By it the angle
between the two bones is increased or diminished. It may take place in four
directions: forward and backward, consisting of flexion and extension; or
inward and outward from the medial line of the body, consisting of
adduction and abduction. Abduction of a limb is movement away from the
medial line of the body. Adduction of a limb is movement toward the
medial line of the body.
Circumduction is that limited degree of motion which takes place
between the head of a bone and its articular cavity, whilst the extremity and
sides of the limb are made to circumscribe a conical space, the base of
which corresponds with the inferior extremity of the limb, the apex with the
articular cavity; this kind of motion is best seen in the shoulder- and hip-
joint.
Rotation is the movement of a bone upon an axis, which is the axis of the
pivot on which the bone turns, as in the articulation between the atlas and
axis, when the odontoid process serves as a pivot around which the atlas
turns; or else is the axis of a pivotlike process which turns within a ring, as
in the rotation of the radius upon the humerus.
Pronation is a form of rotation in which the inferior extremity of the
radius passes before the ulna, and thus causes the hand to execute a kind of
rotation from without inward.
Supination is a form of rotation in which the movement of the forearm
and hand are carried outward so that the anterior surface of the latter
becomes superior.
The Ligamentous Structure.—Ligaments are dense, fibrous, connecting
structures. They are made up principally of white fibrous tissue and exist in
all true joints.
There are four kinds of ligaments associated with true joints:
The first kind, the capsular ligament which encloses all true joints, is thin
and consists of interlaced fibers attached to the bone at the edges of the

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articular cartilages. It either partly or wholly surrounds the joint, enclosing
and protecting a synovial apparatus, which, by secreting a liquid resembling
serum, lubricates the joint to prevent friction.
The second kind, the binding or lateral ligaments, consist of flattened or
rounded cords or bands of fibrous tissue. Such a ligament extends from one
bone to the other, and firmly attached to their roughened surfaces, holds the
bones in place and at the same time allows the required amount of motion.
The third kind, located between the joints, is called interosseous
ligament.
The fourth kind, called the annular ligament binds down and protects the
tendons.
Ligaments of the Ear[2].—The concha of the ear is provided with a
superior and an inferior ligament.
2. The classification of Gadow is used.

Ligaments of the Jaw.—The articulations of the lower jaw are complex.
The freely movable articulation is between the inferior maxilla and the
quadrate. Less freely movable articulations are formed by the quadrate with
the temporal, the zygomatic and the pterygoid. A lateral ligament of the jaw,
the articulo-jugale extends from the posterior border of the inner wing of
the os articulare of the inferior maxilla (Fig. 8, No. 10, and Fig. 19, No. 15)
to the outer border of the os quadrato jugulare.
A lateral temporo-maxillary ligament extends from the outer surface of
the temporal bone to the outer border of the os articulare of the inferior
maxilla (Fig. 8, No. 11, and Fig. 19, No. 14).
Ligaments of the Vertebræ.—In each space between the bodies of the
vertebræ there is a meniscus intervertebralis. This meniscus is analogous to
the annulus fibrosus of mammals (Gadow), which, is possibly formed as a
protrusion of the anterior surface of the vertebral body. The meniscus or
disc may develop into a ring-shaped structure, the true meniscus, or it may
develop to different degrees as an extension of the vertebral body surface,
and become, as in the dorsal and lumbar regions, fused with the vertebral
segments, in which case it is called the annulus fibrosus.
The vertebral disc which is connected with the atlas and which is fused
with that bone, represents the first meniscus, which is called the ligamentum

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transversum atlantis. This, as well as other ligaments of the spinal column,
may become ossified.
The ligament which is located between those vertebral bodies which face
each other and is inside the joint cavity, is called the ligamentum
suspensorium corporum vertebralium. It passes through the central opening
of the meniscus and lies exactly in the long axis of the body of the vertebra.
The first ligament of the neck is the ligamentum suspensorium dentis
epistrophei. The ligamentum capsulare atlantico-occipitale and the
ligamentum capsulare atlantico-epistrophicum odontoideum are two parts
of the joint capsule of the vertebral body. Other ligaments of this part are
the membranæ obturatoriæ intervertebrales posteriores, which are located
between the semicircular rims of the neck vertebræ.
The ligamentum transversum atlantis surrounds the occipital condyle.
The ligamentum nuchæ is a thin, membranous, ribbon-like structure
which lies between the muscles of the right and those of the left side of the
middle, and the lower part on the posterior of the neck, and ends in
attachments to the superior spines of the cervical vertebræ.
The ligamentum elasticum interspinale profundum and the ligamentum
elasticum interspinale superficiale and the three last named are the
ligaments which keep the neck of the fowl in the s-shape, without the action
of the muscles.
The ligamentum capsulare obliquum connects the facets of the oblique
processes.
Ligaments of the Ribs.—The thick inferior end of the sternal portion of
the true rib has two small articular heads, which articulate with two
depressions in the articular surface of the sternum. This articulation is held
firm by a capsular ligament.
The upper end of the sternal rib forms an almost perfect right angle with
the inferior end of the dorsal rib with which it is connected by a joint
provided with a synovial apparatus and a capsular ligament. This
arrangement allows free movement outward and inward and is the main
joint in respiration.
The upper end of the dorsal portion of the rib articulates with the dorsal
vertebra. The joint formed by the articular head with the body of the
vertebra is provided with a capsular ligament. The tubercle of the rib

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articulates with the facet on the transverse process of the dorsal vertebra,
and is provided with a transverse ligament, called the ligamentum
transversum externum. It is also provided with a capsular ligament.
The ligamentum triangulare connects each processus uncinatus with the
succeeding rib. This ligament is in the form of a membranous sheet, or
aponeurosis.
Ligaments of the Sternum (Fig. 13).—The external and the internal
notches of the sternum are bridged over with a thin membrane which gives
an extensive surface for muscular attachments. The sternal muscles overlie
this portion.

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Fig. 13.—Muscles of the fore extremity.
Inside view. 1, Lateral external process
of sternum. 2, Lateral internal process of
same. 3, Ligament of the external notch.
4, Ligament of the internal notch. 5,
Pectoralis major. 5a, Its fan-shaped
expansion at shoulder-joint laid back. 6,
Pectoralis tertius. 7, The coracoid. 8,
Biceps. 8a, Its long head. 8b, Its short
head. 9, Pectoralis secundus. 10, Rectus
abdominis. 11, Teres et infraspinatus.
12, Deltoid. 13, Capsular ligament. 14,
Teres minor. 15, Coraco-brachialis. 16,
Serratus magnus anticus. 17, Extensor
metacarpi radialis longior. 18, Pronator
brevis. 19, Flexor carpi ulnaris. 20,
Flexor carpi ulnaris brevior. 21, Flexor
digitorum profundus. 22, Extensor
indicis longus. 23, Extensor ossis
metacarpi pollicis. 24, Humerus. 25,
Shoulder. 26, Elbow. 27, Carpus. 28,
Section through vertebra. 29, Keel of
sternum. 28a, Flexor brevis pollicis.
29a, Extensor proprius pollicis. 30,
Flexor minimi digiti brevis. 31,
Interosseous palmaris. 32, Interosseous
palmaris.

The sternum is connected by a fibrous mass with the inferior portion of
the clavicle, or hypocledium (Fig. 57), the claviculosternal ligament.

Page 59

The inferior narrow elongated end of the coracoid forms with the sternum
a true articulation, which is provided with a capsular ligament, the
ligamentum capsulare. Capsular ligaments occur at the articulations
between the sternum and ribs.
Ligaments of the Shoulder-joint (Fig. 13).—The shoulder-joint is made
up of the scapula, the humerus, and the coracoid. The ends of these three
bones form the foramen triosseum (Fig. 15, No. A, 7) through which passes
the tendon of the elevator muscle of the wing.
The furcula, independent of the shoulder-joint or girdle, is attached to the
supero-internal part of the proximal end of the coracoid by fibrous
connective tissue; it is also connected to the other bones of the shoulder-
joint by the ligamentum coraco-furculare and the ligamentum furculo-
scapulare.
The ligamentum coraco-scapulare extends from the tuberosity of the
furcula to the coracoid and to the processus furcularis of the scapula.
The ligamentum coracoido-scapulare externum extends between the
external tuberosity of the coracoid, the tuberosity of the scapula, and the
humerus.
The ligamentum coracoideo-scapulare inferius extends from the coracoid
to the inner tubercle of the scapula.
Another long, broad ligament belongs to the episternal apparatus.
The shoulder-joint is provided with a wide, loose, capsular ligament
(Fig. 13, No. 13). Attached to the humerus are four other ligaments, of
which three pass from the anterior end of the coracoid and the fourth from
the scapula. The latter are as follows: first, the supero-anterior ligamentum
humero-coracoideum, which extends from the small tubercle of the
humerus to the coracoid bone; second, the antero-inferior ligamentum
humero-coracoideum, which extends from the humerus to the coracoid;
third, the ligamentum coraco-humerale, which extends from the coracoid to
the large tubercle of the humerus; fourth, the ligamentum humero-scapulare
which extends between the processus humeralis of the scapula and the head
of the humerus.
Ligaments of the Elbow-joint (Fig. 14).—The elbow-joint is made up
of the ulna, radius and the humerus. The ligaments of the elbow-joint are as
follows: the ligamentum capsulare cubiti, or capsular ligament, which

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extends from the processus cubitalis of the humerus to the processus
olecranalis coracoideus of the ulna and to the tuberositas radii of the radius
(Fig. 15, No 5).
The ligamentum laterale cubiti externum connects the outer humeral
distal extremity with the head of the radius (Fig. 15, No. 2).
The ligamentum laterale cubiti internum lies between the inner distal
extremity of the humerus and the tuberculum internum of the ulna (Fig. 14,
No. 9).
The ligamentum annulare radii originates on the olecranon, surrounds
the head of the radius, and is attached to the tuberculum internum of the
ulna (Fig. 15, No. 3).
The ligamentum cubiti teres extends from the head of the radius to the
upper end of the ulna (Fig. 15, No. 4).

Fig. 14.—Muscles and ligaments of the
arm and forearm of a hen.

A. External view. 1, Expansor
secundarium. 2, Tensor patagii longus.
3, Tensor patagii brevis. 5, Brachialis
anticus. 6, Pronator longus. 7, Supinator
brevis. 8, Extensor indicis brevis. 10,
Scapulo-humeralis.

B. Internal view. 9, Ligamentum laterale
cubiti internum.

The ligamentum transversum spreads out between the head of the ulna
and the radius, thus uniting the two bones, and limiting supination (Fig. 15,

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No. 1).
Ligaments of the Carpal Joint.—The carpal joint is made up of the
ulna, radius, the two carpal bones and the metacarpus.
There are two strong ligamenta obliqua carpi ulnaris which extend from
the processus styloideus of the ulna to the tuberculum posterius carpi
ulnaris of the os carpi ulnaris.
The ligamentum posticum ulnare carpi ulnaris extends from the
processus styloideus of the ulna to the os carpi ulnaris.

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Fig. 15.—Ligaments of the arm and
forearm of a hen.

A. The scapulo-coraco-humeral
articulation. 1, Proximal end of the
humerus. 2, Articular head of humerus.
3, The coracoid. 4, Proximal end of the
clavicle. 5, Tendon of pectoralis tertius.
6, Tendon of pectoralis secundus. 7,
Opening or foramen triossium through
which the tendon of the elevator of the
wing passes. (Pectoralis secundus.) 8,
Broken end of scapula.

B. 1, Ligamentum transversum. 2,
Ligamentum laterale cubiti externum. 3,
Ligamentum annulare radii. 4,
Ligamentum cubiti teres. 5, A portion of
the ligamentum capsulare cubiti. 6,
Distal extremity of humerus. 7, Ulna. 8,
Radius.

C. Muscles of the outside surface of the
arm. 1, Tensor patagii longus. 2,
Extensor digitorum communis. 3,
Tensor patagii brevis. 4, Anconeus. 5,
Flexor carpi ulnaris. 6, Biceps. 7,
Triceps. 8. Deltoid. 9, Brachialis
anticus. 10, Flexor metacarpi radialis.
11, Extensor ossis metacarpi pollicis.
12, Extensor metacarpi radialis longior.
13, Extensor indicis longus.

The ligamentum ulnare carpi radialis is a short ribbon-like ligament
which passes over the above-mentioned ligaments and is attached to the
inner surface of the os carpus radialis.

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The ligamentum ulnare carpi radialis internum is a strong ligament
which originates on the inner part of the elbow. It extends to the upper rim
of the base of the main digit.
The ligamentum radiale carpi radialis externum originates on the outside
of the head of the middle digit and inserts to the superior tuberculum carpi
radialis of the radius.
The ligamentum carpi radialis internum, a short ligament, extends from
the inside of the head of the main digit to the inner rim of the carpi radialis.
The ligamentum carpi interosseum is located between the carpal bones.
The ligamentum ulnare metacarpi internum is spread out between the
processus styloideus of the ulna and the tuberositas muscularis on the upper
side of the middle finger base at a point where the second and the third
metacarpi separate.
The ligamentum ulnare metacarpi externum extends from the tubercle of
the distal extremity of the ulna, on the dorsal side, to the tubercle on the
base of the metacarpus.
Ligamentum radiale metacarpi extends from the head of the inner digit to
a point near the tuberculum muscularis of the radius.
The ligamentum transversum ossis carpi radialis et metacarpi is located
between the inferior tuberculum ossis carpi radialis and the first metacarpal
bone.
There is another ligament between the tuberculum superiorus carpi
radialis and the first metacarpal bone.
The ligamentum ossis carpi radialis internum et metacarpi extends from
the inner surface of the carpus radialis to the tuberositas muscularis of the
radius.
The ligamentum ossis carpi ulnaris externum et metacarpi extends from
the ulnar carpal bone to the tuberculum of the metacarpal bone.
The ligamentum ossis carpi ulnaris internum et metacarpi extends from
the processus uncinatus of the ulnar carpal bone to the tuberositas
muscularis of the metacarpal bone.
Ligaments of the Finger.—The ligamentum pollicare connects the
thumb with the first metacarpal bone.

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The ligamentum anterius ossis metacarpi et primæ phalangis digiti
secundi extends from the tuberculum articulare metacarpi, of the proximal
end of the metacarpus, to the tuberculum articulare of the first phalanx of
the second or large finger. Similarly attached, are also an internal and a
posterior ligament, or ligamentum internum and ligamentum posterius.
The three phalanges are all provided with capsular ligaments, or
ligamenta capsularia, which bind together the several phalanges.
The small or third finger is connected to the metacarpus by a capsular
ligament, the ligamentum capsulare, and by an interosseous ligament, or
ligamentum interosseum digitorum, to the first phalanx of the second finger.
Ligaments of the Pelvis.—The obturator foramen, formed by the ilium
and the ischium, is covered by a broad membranous ligament (Fig. 4, No.
29).
The oblong foramen, or foramen oblongum, and the foramen
ischiadicum, formed by the ischium and the pubis are covered by broad
membranous ligaments (Fig. 4, Nos. 29 and 60).
Poupart’s ligament or ligamentum Poupartii, quite small in fowls,
extends from the anterior lower rim of the ilium to the pelvic cavity, and is
inserted at the bottom of the acetabulum.
Another broad ligament originates from the posterior rim of the ischium
and is attached to the square surface of the first coccygeal vertebra.
The ilio-pubic ligament extends from the pubic spine to the last
rudimentary rib.
Ligaments of the Hip-joint (Fig. 25, F).—The hip-joint is made up of
the ilium, ischium, pubis and femur and is a deep ball-and-socket joint. The
cavity or acetabulum is called a cotyloid cavity.
The hip-joint is provided with three ligaments.
The ligamentum capsulare femoris is attached around the rim of the
cotyloid cavity and around the rim of the articular head of the femur (Fig.
25, No. F, 4).
The ligamentum teres, or round ligament, is a very short ligament which
closes the hole at the floor of the cotyloid cavity, at which point it is
attached. It is also attached to the head of the femur.

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The ligamentum ilio-sacrale strengthens the hip-joint capsule. It passes
from the lower anterior rim of the os ilii, extending over the capsule to the
neck of the femur to which it is attached.
The Ligaments of the Knee-joint (Figs. 16 and 17).—The knee-joint is
made up of the femur, patella, tibia and fibula, and is provided with the
following ligaments:
The ligamentum extero-laterale genu is a strong ligament extending from
the condylus externus femoris, or external femoral condyle to the outer
surface of the head of the fibula, or capitulum fibulæ. From this head there
passes inward, a strong ligament to a point between the femur and fibula
(Fig. 25, No. D, 4).

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Fig. 16.—Ligaments and muscles of the hind extremity.

A. A transverse section through the tibial or tarsal cartilage, front view. 1,
Gastrocnemius tendon. 2, Flexor perforatus annularis primus pedis. 3, Flexor
perforans digitorum profundus. 4, Flexor perforatus indicis secundi pedis. 5,
Extensor longus hallucis. 6, The articular surface. 7, Ligamentum capsulare ossis
tarsi. 8, Flexor perforatus medius secundus pedis. 9, Flexor perforatus indicis
secundus pedis. 10, Tendons of the extensor muscles.

B. Knee-joint. Inside view of femoro-tibial articulation. 1, Anterior ligamentum
cruciatum. 2, Internal ligamentum laterale genu. 3, Anterior patellar ligament. 4,
Patella. 5, Distal end of femur. 6, Proximal end of tibia. 7, Location of meniscus
or pad of fibrocartilage.

C. Anterior view of tibio-tarsal articulation. 1, Distal end of tibia. 2, Its articular
surface. 3, Ligamentum anticum. 4, Proximal end of metacarpus. 6, Pad of
fibrocartilage.

D. The dorsal surface of the coccyx. 1, The bilobate oil gland. 2, Its duct. 3,
Levator coccygis.

E. Inside view of pelvis and thigh. 1, Obturator internus. 2, Ambiens. 3, Vastus
internus. 4, Internal ligamentum laterale genu. 5, Tibialis anticus. 6, Loop
through which the tibialis anticus passes. 7, Adductors of the thigh. 8, Loop for
the extensor tendon.

The ligamentum intero-laterale genu extends from the outer surface of
the internal condyle of the tibia, or condylus internus tibiæ. It gives off a
thin ligamentous slip which enters the joint and is attached to the inner half-

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moon shaped pad of fibrous cartilage, or meniscus, which it draws
backward by the flexion of the knee (Fig. 16, No. B, 2).
The ligamentum popliteum arises from the fossa poplitea of the distal
extremity of the femur and extends downward to the posterior rim of the
head of the tibia.
The anterior ligamentum cruciatum genu originates from the fossa
poplitea and extends outward antero-laterally to the rim of the head of the
tibia (Fig. 25, No. 6).
The posterior ligamentum cruciatum genu is a short, strong ligament
which originates from the cavity of the internal condyle of the femur, or
condylus internus femoris, and inserts into the internal glenoid cavity of the
tibia (Fig. 25, No. 1) or cavitas glenoidalis interna.
The meniscus of the femoro-tibial articulation is divided into four parts,
as follows: first, the internal adhesio cornu antici cartilaginis lunatæ;
second, the posterior adhesio cornu antici cartilaginis lunatæ; third, the
external cornu cartilaginis lunatæ; fourth, the anterior cornu antici
cartilaginis lunatæ. The latter originates between the condyles and passes
around the ligamentum cruciatum genu posticum (Fig. 16, No. B, 7).
The inner semi-lunar fibrous cartilage is well developed and is joined by
two ligaments between the femoral and the tibial surfaces (Fig. 25, No. 1).
The external semi-lunar cartilage lies in a cavity between the external
femoral condyle and the head of the fibula (Fig. 25, No. 2).
The fibrous cartilages are bound posteriorly by a ligament, and by a
second ligament to the head of the fibula, or capitulum fibulæ. Both pads of
fibrous cartilage are connected by a transverse ligament called the
ligamentum transversale commune (Fig. 25, No. 5).
The patella is provided with several ligaments, as follows:
The anterior patellar ligament, broad, strong, and irregular in thickness,
extends from the inferior margin of the patella to the rim of the second tibial
crest (Fig. 16, No. B, 3).
The ligamentum capsulare capituli fibulæ is spread out between the head
of the fibula, or capitulum fibulæ, and the superficies glenoidalis peronea
tibiæ.

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Fig. 17.—Muscles and tendons of the
head and posterior extremity.

A. Section of neck with superficial
muscles removed. 1, Obliquo-
transversales. 2, Interspinales. 3,
Intertransversales. 4, Interarticulares.

B. Head showing muscles. 1, Beak. 2,
Nostril. 3, Tongue. 4, Sublingual
salivary gland. 5, Pterygoideus. 6,
Stylo-hyoideus. 7, Temporal. 8, Flexor
capitis inferior. 9, Rectus capitis
lateralis. 10, Rectus capitis posticus
major. 11, Trachelo-mastoideus. 12,
Eye. 13, Mylo-hyoideus. 14, Genio-
hyoideus. 15, Biventer maxilla. 16,
Digastricus. 17, Rectus capitis anterior
minor.

C. Foot of hen showing tendons. 1,
Flexor perforans digitorum profundus.
2, Flexor perforatus medius primus
pedis. 3, Sheath at joint through which
tendon passes. 4, Flexor perforatus
indicis primus pedis. 5, Flexor
perforatus medius secundus pedis. 6,
Flexor perforatus annularis primus
pedis. 7, Flexor longus hallucis.

D. Outside view of leg of hen. 1, Biceps
flexor cruris. 2, Semitendinosus. 3,
Loop through which biceps flexor cruris
passes. 4, Tibialis anticus. 5, Flexor
perforatus indicis secundus pedis. 6,
Flexor perforatus medius primus pedis.

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7, Gastrocnemius. 8, Flexor perforatus
annularis primus pedis. 9, Flexor
perforatus medius secundus pedis. 10,
Extensor longus hallucis.

The ligamentum tibio-fibulare extends from the head of the fibula, or
capitulum fibulæ, to the inner surface of the external crest, or crista externa
tibiæ, of the tibia (Fig. 25, No. 3).
The ligamentum interosseum is a delicate ligament located between the
tibia and fibula (Fig. 25, No. 4) which very early becomes ossified.
Ligaments of the Tibio-metatarsal Joint (Fig. 16).—The tibio-tarsal
joint is made up of the tibia and metatarsus.
The ligamentum capsulare ossis tibio-metatarsi connects the tibia and the
metatarsus and surrounds the joint (Fig. 16, Nos. A, 7 and C, 7).
The ligamentum externum, a long strong ligament, originates on the
upper and outer surface of the external condyle, or condylus externus of the
tibia and is attached to the upper rim of the os metatarsi (Fig. 23, No. 15).
The ligamentum anticum is spread out between the fossa
intercondyloidea of the tibia and the tuberculum ossis metatarsi of the
proximal end of the metatarsus (Fig. 16, No. C, 3). Just posterior to this
ligament, there is an interosseous ligament, the ligamentum interosseum.
A semi-lunar pad of fibrous cartilage, the cartilago semi-lunaris is
located between the outer distal extremity of the tibia and upper articular
surface of the metatarsus (Fig. 16, No. C, 6). Its concave portion is directed
anteriorly and receives an insertion from the ligamentum externum, or
external ligament.
The tendon Achillis (Fig. 16, No. A, 1) may become ossified.
Ligaments of the Toes (Fig. 16).—In addition to the capsular ligaments,
which all true joints have, we find the following in connection with the
toes:
The ligamentum superius and the ligamentum inferius connect the second
toe with the great toe, or hallux.
The ligamentum laterale externum and the ligamentum laterale internum
unite the bases of the second, third and fourth toes to the lateral faces of the
trochleas of the inferior extremity of the metatarsus.

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The bases of the toes are held together by the ligamenta transversa. All
the rest of the toes are held together by the ligamenta capsularia digitorum
pedis and by two lateral ligaments, namely: the ligamentum laterale
externum and the ligamentum laterale internum.

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MYOLOGY

Kinds and Structure of Muscles.—Muscles are highly specialized
structures which have the property of contractility when stimulated, and
thus produce motion. Muscular tissue is sometimes called flesh. Two kinds
of muscles are recognized; muscles of locomotion and visceral muscles.
The muscles of locomotion may be in masses of different shape attached
to the skin, the dermal, or to the skin and skeletal structure, the dermo-
osseous, or from one bone to another, the skeletal. The visceral muscles
form sheets and make up a portion of the wall of many of the hollow
organs, such as the intestines, the stomach, the gizzard, the esophagus, and
the blood-vessels. A special type of muscle forms the heart.
When classified with reference to structure, muscular tissue is divided
into three types, as follows: voluntary-striated, involuntary, and
involuntary-striated. The microscopic examination of each of these types of
muscle shows it to be made up of fibers, these fibers to be made up of
muscle cells, the muscle cell to be inclosed in a delicate tubular sheath, or
membrane, called the sarcolemma. This membrane, tough and elastic,
isolates each fiber. The bundles of fibers, called fasciculi, are surrounded by
a fibrous sheath, which is called the perimysium internum; and the entire
muscle has likewise an investing sheath of connective tissue, called the
perimysium externum. The muscular cells show a longitudinal striation
marking the fibrillæ, and they also show a cross striation. Nuclei are found
just beneath the covering, or sarcolemma, in the striated muscle cell (Fig.
77, No. 2). In the involuntary and in the involuntary-striated muscle cell,
the nuclei are centrally located.
The voluntary-striated muscles consist of cylindrical fibers and with a
few exceptions, are under the control of the will. A muscle of this type, the
regular skeletal form, usually has at each extremity a fibrous structure,

Page 72

called a tendon, by means of which it is attached to the bones. The
intermediate fleshy portion of the muscle, in case of considerable bulk, is
called the belly of the muscle.
The involuntary, non-striated, or smooth muscle, cells are spindle-
shaped, long, and pale in color (Fig. 77, No. 1). The cells lie end to end
forming fibers. These fibers do not terminate in tendons, but are arranged in
sheets and aid in forming the walls of the digestive tract, to which they give
the power of contraction and expansion.
Involuntary-striated, or heart muscle (Fig. 77, No. 4), occupies an
intermediate position between the two muscles just described. It is
composed of cells which branch, are somewhat rectangular. They possess
both longitudinal and transverse striation. Among the fibers is found a small
amount of connective tissue, as in the former types of muscle, which gives
support to the blood-vessels and nerves.
Fascia.—The term fascia is applied to membranous expansions, differing
materially in strength, texture, and relations. Fascia is composed of loosely
arranged white fibrous connective tissue. At least two layers may usually be
distinguished, the superficial fascia and the deep fascia.
Below the skin is the superficial fascia, which forms a continuous
covering over the whole body and serves to attach the skin to the underlying
structure.
The deep fascia more densely constructed, may be attached to the
skeleton, ligaments, and tendons.
When the fascia spreads out, becomes denser, and acts as a continuation
of a muscle, it is called an aponeurosis.
The Muscular Nomenclature.—In the fowl there are 162 muscles,
single or in pairs. These muscles are named from their location, as the
lingualis; others from their attachments, as the dermo-temporalis; some
from their form, as the rhomboideus; others from their use, as the flexor or
extensor; and still others from their direction, as the transversus.

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The Dermal Muscles

Birds are provided with a system of delicate muscles divided into
numerous fasciculi, which harmoniously act upon the feather quills and
collectively agitate the plumage. These are the dermal muscles. This group
is divided into two subgroups: the true dermal muscles, that is, those that
have their origin and insertion to the under surface of the skin; and the
dermo-osseous, those that originate on the surface of some bone and insert
to the inner surface of the skin.

TRUE DERMAL MUSCLES

Dermo-frontalis
Dermo-dorsalis
Dermo-tensor patagii
Dermo-humeralis
Dermo-pectoralis

Dermo-frontalis.[3] Location.—This muscle is somewhat rudimentary
and may be entirely absent. It is located in the frontal region and is about 2
or 3 centimeters long and not so wide.
3. The classification of Shufeldt is used.

Origin and Insertion.—Closely attached to the skin.
Shape.—Flat and rather rectangular.
Relations.—Superiorly with the skin and inferiorly with the frontal
bones.
Action.—By contraction the feathers on the top of the head lie flat. Those
above the eyes are elevated.
Dermo-dorsalis. Location.—In the median line of the neck and back.
Origin and Insertion.—Adhering closely to the skin, it generally
becomes lost at the occiput; it is most highly developed in the mid-cervical
region, and it gradually disappears over the caudal region.

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Shape.—Delicate and ribbon-shaped.
Relations.—Superiorly it is attached to the skin. Fat sometimes surrounds
the muscle.
Action.—By contraction it raises the feathers along the superior part of
the neck and dorsal region.
Dermo-tensor Patagii. Location.—Between the root of the neck and top
of the shoulder.
Origin and Insertion.—Attached to the skin in the region of the anterior
part of the root of the neck, some fibers passing obliquely upward and blend
with fibers of the dermo-temporalis. It blends, by a slender tendon, with that
of the tensor patagii longus.
Shape.—A bundle of muscular fibers later becomes thin, delicate, and
triangular in shape.
Relations.—Externally to the skin.
Action.—Auxiliary to the tensor patagii longus. A tensor of this region.
The patagii are associated with the wing fold of skin which fills the angle
between the arm and forearm. This fold contains elastic tissue and muscle.
Dermo-humeralis. Location.—Lateral thoracic region.
Origin and Insertion.—Fan-like delicate fibers from the skin in the
abdominal integument, contracting into a long narrow fasciculus of fibers,
again spreading out in fan-shape to be inserted to the tendon of the
pectoralis major, just below its insertion.
Shape.—Triangular, fan-shape.
Relations.—Superiorly with the skin.
Action.—Controls the skin in this region. The anterior end being fixed,
the muscles are raised; and the posterior end acting as the fixed point, the
feathers are caused to lie close to the body.
Dermo-pectoralis. Location.—On each side of the chest, lying in a
longitudinal manner.
Origin and Insertion.—Attached to the skin on either side of the thorax
corresponding to the dermo-dorsalis. Anteriorly it disappears over the
region of the origin of the cleido-trachealis, and posteriorly just behind the
tips of the post-pubic parts of the pelvis.
Shape.—Thin, delicate.

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Relations.—Superiorly with the skin.
Action.—The anterior part acting as the fixed point, the feathers of the
chest are raised; and the posterior end acting as the fixed point, the feathers
are made to lie flat.

THE DERMO-OSSEOUS MUSCLES

Dermo-temporalis
Platysma myoides
Dermo-cleido dorsalis
Cleido-trachealis
Dermo-spinalis
Dermo-iliacus
Dermo-ulnaris

Dermo-temporalis (Fig. 18, No. 1). Location.—From the temporal
region down the side of the neck to the anterior part of the thoracic region.
Origin.—By a broad tendinous attachment from a small depression
above and anterior to the temporal fossa. From here the fibers pass upward
and backward and then downward.
Insertion.—A few fibers blend with those of the cleido-trachealis. The
fibers are then lost upon the skin in front and opposite the shoulder-joint.
Some of the fibers blend with those of the dermo-tensor patagii.
Shape.—Long, flat, and ribbon-shaped. The lower portion consists of
delicate fibers.
Relations.—Superior to the temporal muscle and sphenotic process.
Superior to the cleido-trachealis and inferiorly to the shoulder-joint. The
superior portion touches the skin throughout its entire length.
Action.—A tensor of the lateral cervical integument. It is an auxiliary to
the tensor patagii.
Platysma Myoides. Location.—The inferior portion of the throat.
Origin.—From the lower margin of the rami of the jaw. Just inferior to
the attachment of the masseter.

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Fig. 18.—Muscles of the upper neck
region, 1, Dermo-temporalis. 2, Cornu
of the os hyoideum. 3, Carotid artery. 4,
Jugular vein. 5, Pneumogastric nerve. 6,
Esophagus. 7, Trachea.

Insertion.—From the point of origin it spreads out into a thin fan-like
layer and meets its fellow in the median raphe. It is attached to the skin in
this region.
Shape.—A very thin fan-shaped muscle.
Relations.—Closely adherent to the skin.
Action.—Assists in supporting the lingual apparatus and superior larynx.
Compresses and elevates the part.
Dermo-cleido Dorsalis. Location.—Anterior shoulder region.
Origin.—From the upper mesial part of the clavicular bone.
Insertion.—Three fasciculi forming a fan-like arrangement attached to
the skin in the shoulder-joint and scapular region. The extremities of the
fasciculi may meet in the median line of the dorsal region and merge with
the dermo-dorsalis.
Shape.—Three fasciculi forming a fan-shaped radiation.

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Relations.—Superiorly with the skin. Inferiorly with the shoulder-joint.
Action.—Contracting with the origin as the fixed point, they brace the
skin over the forepart of the back. With the integumental attachment as the
fixed point, they aid in the act of respiration.
Cleido-trachealis. Location.—Extending from the shoulder to the
superior laryngeal region.
Origin.—From a small area on the antero-inner part of the middle of the
arm of the furcula.
Insertion.—The fibers pass upward and become flattened and attached to
the skin and dermo-temporalis muscle. They touch each other on the
anterior border of the superior larynx, the trachea, and the skin over these
parts.
Shape.—A slender bundle of muscles.
Relations.—Superiorly the skin, and internally the larynx and the trachea.
Action.—Controls the skin region of this part of the neck.
Dermo-spinalis. Location.—In the region of the shoulder.
Origin.—In an attenuated fascia from the crest of the neural spines of the
first, the second, and the third dorsal vertebræ.
Insertion.—To the skin in a broad pale stratum, over the scapular region.
Shape.—Thin, pale, and very delicate.
Relations.—Superiorly with the skin, and inferiorly with the shoulder.
Action.—Controls the skin of the region.
Dermo-iliacus. Location.—Along the back on either side of the spine.
Origin.—From the inner angle of the marginal portion of the antero-
dorsal border of the ilium.
Insertion.—Passing forward as a delicate band it spreads out and
becomes lost in the skin of the shoulder region.
Shape.—Thin, delicate, and ribbon-shaped.
Relations.—Superiorly with the skin.
Action.—If the posterior end is fixed, it will cause the feathers to lie close
to the skin. Its action would then be opposite to the dermo-dorsalis.
Dermo-ulnaris. Location.—Outer surface of the anterior upper costal
and the posterior humeral region.

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Origin.—By a thin fascia from the outer part of the third and the fourth
true ribs at the base of their epineural appendages. Also from the fascia
between them.
Insertion.—The fibers pass forward and upward as a thick muscular
bundle and is loosely attached to the skin at a point just back of the
humerus. The tendon later becomes spread out and attached to the fascia as
far as the elbow-joint. It covers the olecranon of the ulna.
Shape.—At first rather thick, fascicular-like; later becomes tendinous;
and at its attachment it becomes spread out over the olecranon.
Relation.—Inferiorly with the ribs and humerus, and externally with the
skin.
Action.—A depressor of the humeral region.

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The Skeletal Muscles

THE MUSCLES OF THE HEAD

Temporal
Masseter
Biventer maxillæ
Entotympanicus
Pterygoideus internus
Pterygoideus externus
Digastricus

Temporal (Fig. 19, No. 4). Location.—Occupies the temporal fossa.
Origin.—From the mesian line of the sphenotic process, and the adjacent
wall of the orbit.
Insertion.—The fibers passing downward and forward blend with the
fibers of the masseter. Inferiorly it inserts by a tendon to the coranoid
process upon the superior ramal margin of the mandible.
Shape.—Fan-shaped with broad portion uppermost.
Relations.—It occupies the temporal fossa. It is related superiorly with
the dermo-temporalis and skin. Inferiorly, with the biventer maxillæ and the
masseter.
Action.—It aids in closing the jaw.
Masseter (Fig. 19, No. 1). Location.—Occupies the supero-lateral
portion of the surface of the lower jaw.
Origin.—In two portions: the first, by a broad and thin tendon from the
entire length of the bony ridge above the external auditory meatus, from the
squamosal process, and from the outer portion of the quadrate bone; the
second, from the side and under border of the zygoma.
Insertion.—The first portion: The fibers pass downward and forward
beneath the zygoma; a few of the fibers blend with those of the temporal;
one tendon inserts to a small tubercle on the upper border of the jaw behind

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the coronoid process, and by fleshy insertion to the outer side of the ramus
of the lower jaw, quite as far forward as the horny portion of the beak. The
second portion: by a small tendon to the mandible on its upper border
immediately in front of the articular portion.
Shape.—Flat, and elongate. Somewhat fleshy.
Relations.—Superiorly with the temporal, and inferiorly with the
biventer maxillæ and stylo-hyoideus. Externally with the skin, and
internally with the jaw bone.
Action.—Aids in closing the jaw.
Biventer Maxillæ (Fig. 19, No. 3). Location.—Covers the outer
posterior portion of the mandible.
Origin.—It arises in two portions: The first, from a ridge bounding the
posterior part of the auditory canal; the second, from a depression of the
mesial side. These two parts blend and extend downward and forward.
Insertion.—To the posterior part of the articular end of the mandible.
Shape.—A curved fleshy mass.
Relations.—Superiorly with the temporal and stylo-hyoideus. Posteriorly
with the digastricus and genio-hyoideus. Internally with the jaw bone, and
externally with the skin.
Action.—It aids in opening the jaw.
Entotympanic. Location.—Posterior to the pterygoid.
Origin.—From the side of the basi-sphenoid and from the base of the
rostrum immediately beyond it.
Insertion.—The fibers pass downward and forward, and insert by a
double tendinous slip. One slip inserts to a spine-like process on the upper
side of the pterygoid, and the other to the quadrato-pterygoidean
articulation.
Shape.—Spindle-shaped.
Relations.—Anteriorly with the pterygoid. Internally and posteriorly with
the basi-sphenoid. Externally with the pterygoideus internus.
Action.—Aids in raising the upper mandible by pulling forward the
quadratus and pterygoidean against the palatines.
Pterygoideus Internus (Fig. 17, No. B, 5). (Synonym.—Pterygoideus
medialis.[4])

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4. According to international veterinary nomenclature.

Location.—A muscular mass at the roof of the mouth.
Origin.—From the major part of the surface of the palatine bone and the
distal head and shaft of the pterygoid and the sphenoidal projection.
Insertion.—By a tendon to the antero-internal part of the articular part of
the mandible.
Shape.—Fusiform with a thick fleshy belly.
Relations.—Superiorly with the palatine, the pterygoid, and the sphenoid
bones. Inferiorly with the skin.
Action.—It aids in closing the jaw.
Pterygoideus Externus. (Synonym.—Pterygoideus lateralis.)
Location.—Supero-external to the pterygoideus internus.
Origin.—From the outer part of the extremity of the orbital process of the
quadrate.
Insertion.—The fibers pass downward, outward and forward and are
inserted to the inner part of the mandibular ramus.
Shape.—A small round bundle.
Relations.—Inferiorly with the pterygoideus internus. Externally with the
inferior maxilla.
Action.—Aids in closing the jaw.
Digastricus (Fig. 17, No. B, 16). Location.—Extends from the basi-
temporal to the side of the neck.
Origin.—From the external lateral angle of the basi-temporal.
Insertion.—Opposite the angle of the jaw the fibers spread out in fan-like
arrangement. The muscle meets its fellow of the opposite side; extends
longitudinally over the superior larynx, for some distance down the neck.
Shape.—Thin and ribbon-shaped.
Relations.—Externally to the platysma myoides. The anterior fasciculi
blend with those of the mylo-hyoideus; internally with the larynx at the
upper part.
Action.—To raise the trachea and hyoid apparatus against the pharynx.

Page 82

THE MUSCLES OF THE TONGUE

Mylo-hyoideus
Stylo-hyoideus
Genio-hyoideus
Cerato-hyoideus
Sterno-hyoideus
Depressor-glossus
Cerato-glossus
Hyoideus transversus

Mylo-hyoideus. Location.—The forepart of the inter-ramal space.
Origin.—From the inner side of the lower jaw at a point just above the
lower border and the inturned edge of the horny sheath of the beak.
Insertion.—By aponeurosis to the under side of the hyoid, on the median
line between the first and the second basi-branchial.
Shape.—Thin, flat, and delicate.
Relations.—Inferiorly with the skin. Thin and rather broad, it meets its
fellow of the opposite side. Laterally with the rami of the jaw. Superiorly
with the hyoid apparatus.
Action.—Lifts the tongue upward against the roof of the mouth.
Stylo-hyoideus (Fig. 17, No. B, 6). Location.—Supero-posterior to the
hyoid apparatus.
Origin.—From the outer portion of the articular enlargement of the lower
jaw.
Insertion.—By a tendon to the basi-branchial of the thyro-hyal.
Shape.—A long transversely flattened fasciculus.
Relations.—Supero-posterior part of the hyoid apparatus along side the
genio-hyoideus and the cerato-hyoideus.
Action.—Singly, pulls the tongue to one side; acting with its fellow, pulls
the tongue upward.
Genio-hyoideus (Fig. 9, No. 7). Location.—Supero-posterior to the
hyoid apparatus.
Origin.—From the anterior portion of the inner side of the lower jaw.

Page 83

Insertion.—To the middle of the outer side of the basi-branchial of the
corner of the os hyoides which cornu it completely envelops.
Shape.—A long, rather thick fasciculus.
Relations.—With the stylo-hyoideus and cerato-hyoideus.
Action.—Protrudes the tongue from the mouth.
Cerato-hyoideus (Fig. 9, No. 8). (Synonym.—Kerato-hyoideus.)
Location.—Inferior to the hyoid apparatus.
Origin.—By a delicate tendinous slip from the under side of the shaft of
the basi-hyal element of the hyoid apparatus.
Insertion.—To a small elevation on the under side of the anterior end of
the glosso-hyal.
Shape.—A small round muscular fasciculus becoming tendinous in its
anterior half.
Relations.—Superiorly with the hyoid apparatus.
Action.—Singly, pulls the tongue to one side; acting with its fellow,
depresses the tongue.
Sterno-hyoideus. Location.—Inferior to the hyoid apparatus.
Origin.—From the outer anterior surface of the thyroid bone of the
superior larynx.
Insertion.—To the anterior part of the basi-hyal.
Shape.—At first broad and rather fleshy, becomes contracted and
somewhat tendinous.
Relations.—Inferior to the hyoid apparatus and superior larynx.
Action.—When the larynx is fixed, acting alone deflects the tongue
laterally; acting with its fellow, depresses the tongue. If the base of the
tongue is fixed the two pull the larynx forward. Hence muscles of
deglutition.
Depressor-glossus. Location.—Superior to the basi-hyal.
Origin.—From the under portion of the basi-hyal.
Insertion.—To under part of the glosso-hyal.
Shape.—Small, short.
Relations.—Superiorly with the basi-hyal and glosso-hyal bones.

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Action.—Depresses the tip of the tongue and elevates the base.
Cerato-glossus. Location.—On the upper portion of the cornu of the
hyoid.
Origin.—One-half of the surface of the first basi-branchial.
Insertion.—To the upper side of the shaft of the cerato-branchial element
of the hyoid apparatus.
Shape.—A small muscular fasciculus.
Relations.—Supero-laterally to the cerato-branchial element.
Action.—Elevates the cornua of the hyoid arches and presses them
against the skull.
Hyoideus Transversus (Fig. 9, No. 9 and 10). Location.—Envelops the
spur process of the euro-hyal.
Origin and Insertion.—It extends from the inner side of one cornu to the
spur process.
Shape.—Thin, flat.
Relations.—Posterior to the euro-hyal, which it envelops, and between
the cornua of the os hyoides.
Action.—Approximates the cornua of the os hyoides.

THE CERVICAL MUSCLES

Complexus
Rectus capitis anticus minor
Flexor capitis inferior
Rectus capitis posticus major
Biventer cervicis
Longus colli posticus
Obliquus colli
Longus colli anterior
Rectus capitis lateralis
Trachelo-mastoideus
Interspinales
Interarticulares
Obliquo-transversales

Page 85

Intertransversales
Scalenus medius
Complexus (Fig. 19, No. 5). Location.—Supero-lateral portion of the
neck.
Origin.—By three tendinous slips from the antero-lateral portion of the
transverse process of the fourth, the fifth, and the sixth cervical vertebræ.
Insertion.—The muscular fibers pass around the neck and meet their
fellows in the median line in a fascia formation. The thin tendinous sheet
inserts into the occiput just above the occipital ridge.
Shape.—From point of origin this muscle expands into a broad sheet.
Relations.—It overlies the muscles of the occipital region.
Action.—It extends the head.
Rectus Capitis Anticus Minor (Fig. 19, No. 8). (Synonym.—Rectus
capitis ventralis minor.)
Location.—Infero-lateral portion of the neck.
Origin.—From the apices of the hyapophyses of the second, the third,
and the fourth cervical vertebræ.
Insertion.—To the occiput just below the complexus.
Shape.—A long and rather thick fasciculus.
Relations.—Externally with the skin. The tendinous slips of origin pass
between the flexor capitis inferior and longus colli anterior.
Action.—Extends the head.
Flexor Capitis Inferior (Fig. 19, No. 7). Location.—Antero-inferior part
of the neck.
Origin.—From the apices of the hyapophyses of the second, the third,
and the fourth cervical vertebræ.
Insertion.—To the triangular area on the basi-temporal of the base of the
cranium.
Shape.—At first tendinous, becomes somewhat fleshy as it passes
forward.

Page 86

Fig. 19.—Muscles of the head and neck. 1, Masseter muscle. 2, Infraorbital
sinus. 3, Biventer maxilla. 4, Temporalis. 5, Complexus. 6, Rectus capitis
posticus major. 7, Flexor capitis inferior. 8, Rectus capitis anticus minor. 9,
Biventer cervicis. 10, Longus colli posticus. 11, Obliquus colli. 12,
Intertransversales. 13, Longus colli anterior. 14, Lateral temporo-maxillary
ligament. 15, Lateral ligament of the jaw. 16, Trachelo-mastoideus. 17, Rectus
capitis lateralis. 18, Scalenus medius. 19, Rhomboideus. 20, Trapezius. 21,
Location of scapula. 22, Supraspinatus. 23, Teres et Infraspinatus.

Relations.—Antero-inferior portion of the neck close to the rectus capitis
anticus minor.
Action.—Flexes the head upon the neck.
Rectus Capitis Posticus Major (Fig. 19, No. 6). (Synonym.—Rectus
capitis dorsalis major.)
Location.—Supero-lateral area on the anterior portion of the neck.
Origin.—From the median anterior aspect of the second cervical
vertebra, and the supero-anterior border of the neural canal.
Insertion.—To the crescent-shaped area at the back of the skull.
Shape.—Short, thick, fleshy bundle.
Relations.—Superiorly with the complexus; inferiorly with the trachelo-
mastoideus and the vertebræ.
Action.—Singly, pulls the head to one side; acting with its fellow, extends
the head.

Page 87

Biventer Cervicis (Fig. 19, No. 9). Location.—Occupies the superior
part of the neck.
Origin.—From the side of the neural spine of the first dorsal vertebra,
and from the adjacent tendon of the longus colli posticus.
Insertion.—To the occiput.
Shape.—Tendinous in the middle with a more or less spindle-shaped
belly at each end.
Relations.—Superior to the longus colli posticus. It lies next to the skin.
Action.—Extends the head on the neck and elevates the neck.
Longus Colli Posticus (Fig. 19, No. 10). (Synonym.—Longus colli
dorsalis.)
Location.—Occupies the superior part of the neck.
Origin.—From the marginal edges of the summits of the neural spines of
the first two dorsal vertebræ.
Insertion.—To the transverse process of the axis, and superior part of the
cervical vertebræ.
Shape.—A long, somewhat narrow, flattened muscle, the inferior portion
of which is divided into five or six fasciculi.
Relations.—Superiorly with the biventer cervicis and inferiorly with the
vertebræ.
Action.—Raises the neck upward.
Obliquus Colli (Fig. 19, No. 11). Location.—On the lateral side of the
neck.
Origin and Insertion.—The first of the seven fasciculi originates from the
diapophysis of the eleventh cervical vertebra, winds obliquely over the
tenth, and is inserted into the posterior margin of the postzygapophysis of
the ninth vertebra. In its passage it receives the slip from the longus colli
posticus. The next fasciculus originates from the transverse process of the
tenth cervical vertebra, winds obliquely over the ninth vertebra, and is
inserted to the postzygapophysis of the eighth vertebra. In its passage it also
receives a fasciculus from the longus colli posticus. The next three fasciculi
originate in a similar manner being attached to similar postzygapophyses
and have slips extending forward which slips are inserted to the neural
spines of the alternate vertebræ. The sixth fasciculus originates from the

Page 88

transverse process of the sixth vertebra, passing obliquely up the neck is
inserted to the extremity of the diapophysis of the fourth vertebra, the outer
extremity of the transverse process of the third vertebra. The seventh, or
anterior, fasciculus originates from the transverse process of the fifth
vertebra, and is inserted to the extremity of the diapophysis of the third
vertebra.
Shape.—Short, thick fasciculi.
Relations.—Laterally with the vertebræ. Inferiorly with the
intertransversales. Superiorly with the longus colli posticus, and externally
with the skin.
Action.—Flexes one vertebra on the other laterally.
Longus Colli Anterior (Fig. 19, No. 13). (Synonym.—Longus colli
ventralis.)
Location.—Occupies the anterior portion of the neck.
Origin and Insertion.—This muscle is divided into a vertical portion, and
a superior and an inferior oblique portion. The vertical portion originates
from the hypophyses of the tenth to the fifteenth vertebra and is inserted by
a tendon to the tubercle on the inferior portion of the atlas. Small, slender
tendons are given off and insert to the apices of the parapophyses of the
fourth to the tenth cervical vertebræ. There is more or less attachment to the
bodies of the cervical vertebræ mentioned. The superior oblique portion
originates from the diapophyses of the third, the fourth, the fifth cervical
vertebræ and becoming tendinous is inserted to the tubercle on the inferior
portion of the body of the atlas. The inferior oblique portion originates from
the transverse processes of the fourth, the fifth, and the sixth cervical
vertebræ. It is inserted by a slender tendon to the apex of the parapophysis
of the third cervical vertebra.
Shape.—A long fleshy muscle extending the entire length of the neck.
Relations.—Inferiorly with the skin and superiorly with the cervical
vertebræ.
Action.—Pulls the neck downward.
Rectus Capitis Lateralis (Fig. 19, No. 17). Location.—The infero-
lateral anterior portion of the neck.
Origin.—Originates tendinous from the diapophysis of the third, the
fourth, and the fifth cervical vertebræ.

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Insertion.—Passes obliquely upward in front of the spinal column to the
inner tubercle on the basal ridge of the basi-temporal bone, by a
subcompressed tendon.
Shape.—A somewhat thick fasciculus.
Relations.—Superiorly with the trachelo-mastoideus, inferiorly with the
longus colli anterior, and externally with the skin.
Action.—Singly, pulls the head down and to one side; acting with its
fellow, pulls the head downward.
Trachelo-mastoideus (Fig. 19, No. 16). (Synonym.—Longissimus
capitis et atlantis.)
Location.—Laterally on the anterior portion of the neck.
Origin.—Semitendinous from the diapophyses of the second, the third,
the fourth, and the fifth cervical vertebræ.
Insertion.—By subcompressed tendon to the base of the cranium, at the
outer tubercle of the basal ridge of the basi-temporal.
Shape.—Flattened from side to side; broad at the posterior portion,
becomes angular at the anterior portion.
Action.—Singly, pulls the head down and to one side; acting with its
fellow, pulls the head downward.
Interspinales (Fig. 17, A, No. 2). Location.—Superior to the vertebra.
Origin and Insertion.—A series of muscles connecting the superior
neural spines of the cervical vertebræ.
Shape.—Thin, flat.
Relations.—Anteriorly the posterior border of the vertebræ in front and
posteriorly the anterior border of the succeeding vertebræ, inferiorly by the
vertebræ.
Action.—To approximate the spinous portion of the vertebræ.
Interarticulares (Fig. 17, No. A, 4). Location.—Supero-laterally to the
vertebræ. Between the postzygapophysis.
Origin and Insertion.—From the posterior margin of the ring of the atlas
to the postzygapophysis of the axis. Then in the succeeding vertebræ from
the postzygapophysis of the vertebra to the same of the succeeding vertebra.
Shape.—Muscular bundle.

Page 90

Relations.—Inferiorly with the vertebræ. Supero-laterally with the
obliquo-transversales.
Action.—Aids in approximating the vertebræ in a supero-lateral
direction.
Obliquo-transversales (Fig. 17, A, No. 1). Location.—Supero-lateral to
the vertebræ.
Origin and Insertion.—Passes obliquely from the transverse process of
one vertebra to the postzygapophysis of the vertebra beyond.
Shape.—A thin fasciculus.
Relations.—Inferiorly with the interarticulares and laterally with the
intertransversales.
Action.—Aids in flexing the vertebræ supero-laterally.
Intertransversales (Fig. 19, No. 12). Location.—Laterally to the
vertebræ.
Origin and Insertion.—Extend between the transverse processes
beginning at the third cervical vertebra.
Shape.—Short, thick.
Relations.—Laterally the vertebræ. Superiorly the obliquo-transversales.
Action.—Aids in flexing the vertebræ laterally.
Scalenus Medius (Fig. 19, No. 18). (Synonym.—Scalenus.)
Location.—Supero-laterally to the entrance of the thorax.
Origin.—From the diapophysis and pleurapophysis of the eleventh
cervical vertebra.
Insertion.—To the entire border of the first rib. A few fibers pass over to
the anterior free margin of the middle third of the second rib.
Shape.—Rather pyramidal in shape with base uppermost.
Relations.—Posteriorly with the levatores costarum. Internally with the
longus colli.
Action.—When the first rib is fixed singly, turns the neck to one side;
acting with its fellow, extends the neck. When the neck is fixed, by drawing
the first rib forward, it acts as an inspiratory muscle.

Page 91

THE MUSCLES OF THE AIR PASSAGES

The Superior Larynx

Constrictor glottidis
Thyreo-arytenoideus

The Inferior Larynx

Tracheo-lateralis
Broncho-trachealis posticus
Broncho-trachealis anticus
Broncho-trachealis brevis
Bronchialis posticus
Bronchialis anticus
Sterno-trachealis

Constrictor Glottidis. Location.—Supero-anterior portion of the
superior larynx.
Origin.—From the superior and longitudinal line of the thyroid plate.
Insertion.—All along the inner margin of the arytenoid bone, and to the
apex of the mid-cricoidal segment.
Shape.—Thin, flat sheet extending outward and upward, and then
inward.
Relation.—Interiorly with the larynx.
Action.—The two muscles of this kind acting together, close the glottis
by drawing the apices of the arytenoids to the median line.
Thyreo-arytenoideus. Location.—Supero-lateral portion of the superior
larynx.
Origin.—From the entire outer margin of the thyroid plate and the outer
margin of the cricoid bone.
Insertion.—All along the outer margin of the arytenoid bone and the
outer border of the central cricoid piece.
Shape.—A thin, flat sheet.
Relations.—Infero-laterally with the superior larynx.

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Action.—The two muscles of this kind acting together, open the glottis
by pulling the arytenoid bone outward.
Tracheo-lateralis (Fig. 20, No. 2). Location.—Along the lateral side of
the trachea.
Origin.—By the union of the bronchio-trachealis posticus and bronchio-
trachealis anticus, on the lateral side of the trachea, about 1½ centimeters
from the bifurcation of the trachea.
Insertion.—In delicate fan-like structure to the side of the trachea, near
the superior larynx.
Shape.—Thin, ribbon-shaped, closely attached to the trachea.
Relations.—Internally with the trachea, and externally with the skin and
other integument.
Action.—Acts as a brace to the sides of the trachea, and contracting,
approximates the tracheal rings and thus shortens the trachea.
Broncho-trachealis Posticus (Fig. 21, No. 3). Location.—Postero-
superior portion of the trachea. The fibers pass downward and backward.
Origin.—From the inferior end of the tracheo-lateralis.
Insertion.—To the end of the third half of the bronchial ring of the same
side.
Shape.—A small fasciculus.
Relations.—Internally with the trachea, and externally with the skin and
other integument.

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Fig. 20.—The anterior pectoral region. 1, Sterno-trachealis. 2, Tracheo-lateralis.
3, Broncho-trachealis brevis. 4, Costal process of sternum. 5, Right and left
carotid converging and occupying same sheath at 6. 7, The heart showing
branches of coronary artery. 8, Cervical air-sac. 9, Left brachio-cephalic artery.
10, Right brachio-cephalic artery. 11, Trachea. 12, Inferior larynx. 13.
Subclavian artery. 14, Carotid trunk. 15, Internal thoracic artery. 16 Thyroid
gland. 17, Anterior vena cava. 18, Auricular appendage.

Fig. 21.—The inferior tracheal region.
1, Bronchialis anticus. 2, Bronchialis
posticus. 3, Broncho-trachealis posticus.
4, Broncho-trachealis anticus.

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Action.—A tensor of the true or inferior larynx.
Broncho-trachealis Anticus (Fig. 21, No. 4). Location.—Anterior
portion of the inferior extremity of the trachea.
Origin.—The anterior branch of the bifurcated tracheo-lateralis.
Insertion.—To the anterior extremity of the third half ring of the
bronchus of the same side.
Shape.—A small fasciculus.
Relations.—Internally with the trachea, and externally with the skin and
other integument.
Action.—A tensor of the inferior larynx.
Broncho-trachealis Brevis (Fig. 20, No. 3). Location.—Posterior part of
the inferior extremity of the trachea.
Origin.—From just beneath the broncho-trachealis anticus muscle.
Insertion.—Extends obliquely across the inferior larynx and is inserted to
the posterior end of the second bronchial ring.
Shape.—Rather short, strong, straight, subcylindrical.
Relations.—Internally with the trachea, and laterally with the broncho-
trachealis posticus.
Action.—A tensor of the inferior larynx.
Bronchialis Posticus (Fig. 21, No. 2). Location.—Supero-lateral side of
the anterior end of the bronchi.
Origin.—From the lateral inferior margin of the last tracheal ring.
Insertion.—Passing obliquely across the larynx it inserts to the posterior
extremity of the second half ring of the bronchus.
Shape.—Small, thick, spindle-shaped.
Relations.—Internally with the trachea, inferiorly with the bronchialis
anticus, and superiorly with the broncho-trachealis brevis.
Action.—A tensor of the larynx.
Bronchialis Anticus (Fig. 21, No. 1). Location.—Inferior to the former
muscle.
Origin.—From the last ring of the trachea.
Insertion.—The fibers pass obliquely forward and become inserted to the
rim of the arytenoid cartilage of the inferior larynx, and the anterior

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extremities of the first and second half rings of the bronchus.
Shape.—Thick, spindle-shaped; about twice the size of the bronchialis
posticus.
Relations.—It is crossed at its origin by the broncho-trachealis anticus
and is related internally with the bronchus and end of the trachea.
Action.—A tensor of the larynx.
Sterno-trachealis (Fig. 20, No. 1). Location.—The inferior region of the
trachea above the above-named muscles.
Origin.—From the side of the trachea beneath the posterior border of the
broncho-trachealis anticus.
Insertion.—Passes downward and backward across the cavity of the
chest and is inserted to the inner part of the costal process of the sternum.
Shape.—A delicate cord of fibers.
Relations.—Internally with the broncho-trachealis muscles.
Action.—A relaxor of the larynx, and hence, of the tympanic membrane.

THE STERNAL GROUP

Triangularis Sterni. Location.—In the floor of the thoracic cavity.
Origin.—From the entire superior margin of the summits of the costal
processes.
Insertion.—The fibers extend upward and backward, dividing into four
digitations which cover the inner surface of the three principal sternal ribs,
and are inserted to the first four as high as their articulations with the
vertebral ribs.
Shape.—Flat and somewhat triangular.
Relations.—Interiorly with the floor of the thoracic cavity.
Action.—A powerful muscle of expiration. In contracting, lessens the
cubic content of the thorax.
The Diaphragm (Fig. 47, No. 10; Fig. 33, No. 9). Description.—The
diaphragm in the domestic fowl is rudimentary. It consists of a thin semi-
transparent membrane, situated between and separating the thoracic and the
abdominal cavities. It readily conforms to the various organs pressing upon

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it from each side. On each side are three rudimentary muscles which extend
from the vertebral heads of the second, the third, and the fourth sternal ribs.
The fibers of these muscles spread out in fan-like upon the diaphragm, and
are seen just above the digitations of the triangularis sterni.

THE ABDOMINAL MUSCLES

Obliquus abdominis externus
Obliquus abdominis internus
Rectus abdominis
Transversalis abdominis

Obliquus Abdominis Externus (Fig. 22, No. 1). Location.—The
outermost muscle of the lateral abdominal wall.
Attachments.—By a delicate aponeurotic membrane, from the sides of all
the true dorsal ribs, from the posterior border of the last vertebral rib and
the adjoining margins of the pelvis, and from the entire posterior surface of
the inferior border of the post-pubic element of the pelvis; by aponeurosis,
blending with the fascia toward the root of the tail and lower part of the
abdomen; and by aponeurosis to the sides of the sternum, to the under part
of the pectoralis major muscle, and to the zyphoid prolongation. Also by
aponeurosis it meets its fellow from the opposite side, at the linea alba.

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Fig. 22.—The abdominal muscles of a hen. Right side. 1, Obliquus abdominis
externus. 2, Obliquus abdominis internus. 3, Peritoneum covering intestines. 4,
Peritoneum covering the gizzard. 5, The lungs (note how small they are from a
relative standpoint). 6, The great sciatic or ischiadic nerve. 7, Lumbar nerves. 8,
Kidney. 9, Brachial plexus. 10, Pericardium of the base of the heart. 11, Anterior
vena cava. 12, Oil gland. 13, Showing a sacculation of the abdominal muscles.
There is no tunica abdominalis in the fowl.

Obliquus Abdominis Internus (Fig. 22, No. 2). Location.—Just internal
with regard to the external oblique.
Attachments.—By aponeurosis, from the posterior third of the post-pubic
element of the pelvis; by muscular fibers, from the balance of the bone; and
by a few fibers, from the iliac border posterior to the acetabulum.
Anteriorly, these fibers are inserted to the entire posterior margin of the last
vertebral rib, and into the pleurapophysial head of the last costal rib.
Rectus Abdominis (Fig. 13, No. 10 and Fig. 23, No. 1). Location.—The
inferior median abdominal wall.
Attachments.—By aponeurosis, from the distal extremity of the post-
pubic element of the pelvis and from the semitendinous ligament which
stretches from one post-pubic tip to the other. Attaches anteriorly to the
zyphoid margin of the sternum, and passes, by a broad aponeurotic
membrane, over the outer surface of the thoracic wall beneath the external
oblique.
Transversalis Abdominis (Fig. 25, No. H, 1). Location.—Infero-lateral
portion of the abdominal wall.
Attachments.—By a thin, tendinous attachment from the entire post-
pubic and iliac margins of the pelvis and from the interpubic ligament. Its

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fibers cross the abdomen between the peritoneum, the rectum, and the
internal oblique. It is inserted over the entire pleural part of the last two
vertebral ribs, the intercostal muscles between them, and the same surface
of the hemapophyses connected below. Inserts into the linea alba.
Action.—The abdominal muscles give support to the abdominal organs,
aid in flexing the spine, draw the last rib backward, thus aiding in
respiration, and compress the abdominal organs to aid in defecation and
expiration.

THE DORSO-LUMBAR REGION

Sacro-lumbalis
Longissimus dorsi

Sacro-lumbalis. Location.—The lateral lumbo-sacral region.
Origin.—Tendinous from the anterior margin of the ilium, from the
angles of the last two vertebral ribs, and by tendinous slips, from the outer
ends of the transverse processes of the last three dorsal vertebræ.
Insertion.—By a few fleshy fibers into the angle of the first dorsal rib
and to the corresponding points upon the free cervical ribs, and by a strong
semitendinous insertion into the outer extremity of the diapophysis of the
twelfth cervical vertebra.
Shape.—A close fitting, tendo-muscular sheet extending between the
anterior margin of the ilium and the root of the neck.
Relations.—Intimately blended with the longissimus dorsi externally.
Action.—Assists the longissimus dorsi.
Longissimus Dorsi (Fig. 24, No. 4). Location.—The superior dorso-
lumbar region.
Origin.—From the inner portion of the anterior margin of the ilium, and
from the various surfaces afforded by its walls and the walls of the ilio-
neural canal; by a series of short and distinct tendons alternately from the
anterior and posterior extremities of the summits of the neural spines of all
the dorsal vertebræ. From the diapophyses of the dorsal vertebræ, from the
crests of the neural spines of the last three dorsal vertebræ, from the bodies
of the dorsal vertebræ, and from the fascia between them and the sacro-

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lumbalis; and also by a tendinous sheet continuous with the origin of the
longus colli posticus.
Insertion.—By four fasciculi into the free posterior margins of the
oblique processes of the eleventh, the twelfth, the thirteenth, and the
fourteenth cervical vertebræ.
Shape.—A large flat sheet.
Relations.—Laterally, with the superior spinous processes of the
vertebræ, and with the superior surface of the ribs.
Action.—Singly, flexes the back laterally; with its fellow, aids in
elevating the body upward.

THE COCCYGEAL MUSCLES

Levator coccygis
Levator caudæ
Transversus peronei
Depressor caudæ
Depressor coccygis
Lateralis caudæ
Lateralis coccygis
Infracoccygis

Levator Coccygis (Fig. 23, No. 2). Location.—The superior part of the
caudal apparatus.
Origin.—From a limited area of the ilium just beyond and to the side of
the anterior free caudal vertebræ.
Insertion.—Into the tuberosity of the anterior margin of the pygostyle.
Shape.—Short, fleshy.
Relations.—Superior portion of the coccygeal vertebræ.
Action.—Elevates the tail.
Levator Caudæ (Fig. 23, No. 4). Location.—Supero-lateral side of the
tail.
Origin.—From the posterior surface of the post-acetabular area of the
pelvis, and from the superior surface of all the coccygeal vertebræ except

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the pygostyle.
Insertion.—To the four inner quill butts of the main tail feathers.
Shape.—Long, spindle-shaped.
Relations.—Internally, with the levator coccygis and externally, with the
lateralis caudæ.
Action.—Powerfully elevates the four inner main tail feathers.
Transversus Peronei (Fig. 23, No. 3). Location.—The posterior
abdominal region.

Fig. 23.—Outer layer of muscles of the
tail and thigh, 1, Rectus abdominis. 2,
Levator coccygis. 3, Transversalis
peronie. 4, Levator caudæ. 5, Lateralis
caudæ. 6, Depressor caudæ. 7, Sartorius.
8 and 9, Gluteus primus. 10,
Semitendinosus. 11, Gastrocnemius. 12,
Peroneus longus. 13, Flexor perforatus
indicis secundus pedis. 14, Flexor
perforatus medius secundus pedis. 15,
Lateral ligament of the hock.

Origin.—From the entire posterior margin of the ischium, and from the
posterior margin of the post-pubis extending beyond it.
Insertion.—Becoming aponeurotic, it passes toward the coccyx and is
attached to the entire posterior margin of the ilium. Passes to the median
line, meeting its fellow in front of the anus.
Shape.—Thin, sheet-like.

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Relations.—Infero-anteriorly with the anus. Posteriorly with the edges of
the ilium and of the ischium. Internally with the depressor caudæ.
Action.—Gives support to the viscera in the post-anal region, and aids in
attaching the anus to the structures above.
Depressor Caudæ (Fig. 23, No. 6). Location.—The infero-lateral side of
the tail.
Origin.—From the lower half of the posterior border of the ischium, and
from the entire posterior border of the post-pubis beyond.
Insertion.—To the quill butts of the three or four outer main tail feathers.
Shape.—Strong, conical.
Relations.—Externally, with the depressor coccygis.
Action.—Singly, pulls the tail downward and outward; with its fellow,
pulls the tail downward.
Depressor Coccygis. Location.—The outermost of the infero-lateral
muscles of the tail.
Origin.—From the lower half of the posterior margin of the ischium and
the anterior three-fourths of the posterior margin of the post-pubic element
of the pelvis beyond it.
Insertion.—To the thickened rim of the inferior and expanded portion of
the pygostyle.
Shape.—Flat, triangular.
Relations.—Internally with the depressor caudæ.
Action.—Singly, pulls the tail downward and to one side; with its fellow,
pulls the tail downward.
Lateralis Caudæ (Fig. 23, No. 5). Location.—The lateral side of the tail.
Origin.—From the tip of the transverse process of the first free caudal
vertebræ.
Insertion.—To the outer three quill butts of the main tail feathers.
Shape.—Four fasciculi forming a fleshy belly.
Relations.—Inferiorly, with the levator caudæ and superiorly with the
depressor caudæ.
Action.—Singly, pulls the tail downward and outward; with its fellow,
pulls the tail downward. The outermost fasciculus contracting, spreads the

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tail feathers.
Lateralis Coccygis (Fig. 25, No. E, 2). Location.—The infero-lateral
side of the caudal vertebræ.
Origin.—From the surface of the posterior end of the ilium and by
tendons from the under side of the ends of the first three or four caudal
vertebræ.
Insertion.—To the side of the posterior margin of the expanded portion of
the pygostyle.
Shape.—Subcompressed mass.
Relations.—With the transverse processes of the caudal vertebra,
inferiorly.
Action.—Controls the lateral movements of the tail and its feathers, and
the oblique downward movement.
Infracoccygis (Fig. 25, No. E, 1). Location.—The extreme inferior
portion of the caudal vertebræ.
Origin.—From the inferior surface of the diapophysis of the last vertebra
which anchyloses with the pelvic sacrum, and from all the free caudal
vertebræ.
Insertion.—Into the lower side of the pygostyle.
Shape.—Flat, somewhat triangular.
Relations.—Superiorly, with the vertebræ, laterally, with the lateralis
coccygis, and mesially, with its fellow of the opposite side.
Action.—Depresses the tail.

THE COSTAL REGION

Latissimus dorsi
Trapezius
Rhomboideus
Serratus magnus anticus
Serratus parvus anticus
Teres et infraspinatus
Intercostales
Levatores costarum

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Appendico-costales
Latissimus Dorsi (Fig. 24, No. 7). Location.—Supero-lateral portion of
the dorsal region.
Origin.—From two portions, the anterior slip from the outer edge of the
superior margins of the neural spines of the second and the third dorsal
vertebræ, and the second portion from a similar point on all the succeeding
dorsal vertebræ. The second portion is fascia-like in its attachments.
Insertion.—The fibers converge toward the humerus and enter between
the deltoid the scapular head of the triceps and the remaining heads of this
muscle and is inserted to the anconal part of the humerus, just within in the
radial crest.
Shape.—Thin, triangular.
Relations.—Superiorly, with the skin. The most superficial of the dorsal
muscles.
Action.—To elevate the humerus and thus flex the shoulder-joint. An
expiratory muscle when the wing is fixed.
Trapezius (Fig. 19, No. 20). Location.—In the shoulder region, just
below the longissimus dorsi.
Origin.—From the neural spines of the second, the third, the fourth, and
the fifth cervical vertebræ just below the latissimus dorsi.
Insertion.—To the mesian upper border of the scapula.
Shape.—A flat oblong layer of fibers.
Relations.—The posterior part of the trapezius overlies the anterior part
of the rhomboideus. The posterior two-thirds is covered by the latissimus
dorsi. The anterior third is superficial.
Action.—Draws the scapula forward.
Rhomboideus (Fig. 19, No. 19). Location.—Supero-posterior scapular
region.
Origin.—From the neural spines of the first four dorsal vertebræ beneath
the latissimus dorsi and trapezius muscles.
Insertion.—The fibers passing outward and backward attach to the
posterior third of the mesial or upper border of the scapula.
Shape.—Thin, flat, delicate.

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Relations.—Superiorly, by the latissimus dorsi and the trapezius.
Action.—To draw the free end of the scapula upward and forward.
Serratus Magnus Anticus (Fig. 13, No. 16). Location.—The supero-
lateral side of the thorax.
Origin.—By three strong digitations: first, from the outer part of the
second true rib just above the base of the epineural appendage; the other
two, from similar locations on the two succeeding ribs, just above the origin
of the dermo-ulnaris.
Insertions.—The first by tendinous attachment to the
interpleurapophysial membrane. The rest of the fibers pass upward and
slightly forward, and are inserted to the inferior surface of the apex of the
scapula.
Shape.—Three flat, strong digitations.
Relations.—Internally, with the ribs.
Action.—If the scapula is fixed, it is a muscle of inspiration.
Serratus Parvus Anticus. Location.—The outer and upper surface of the
anterior part of the thorax.
Origin.—By three digitations from the outer surface of the first three ribs
above the origin of the serratus magnus anticus and the thoraco-scapularis.
Insertion.—The thin sheet of fibers passes upward and backward, and is
inserted to the inferior margin of the scapula.
Shape.—Thin, flat.
Relations.—Internally, with the ribs.
Action.—If the scapula is fixed, it is a muscle of respiration.
Teres et Infraspinatus (Fig. 13, No. 11). Location.—Scapular region.
Origin.—From the superior surface and outer margin of the posterior
two-thirds of the scapula.
Insertion.—The fibers pass forward and outward, and insert to the
humerus at the middle of the ulnar margin of the pneumatic fossa, between
the forks of the triceps.
Shape. —Flat, triangular-shaped.
Relations.—Anteriorly, with the supraspinatus. Internally, with the ribs.

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Action.—Aids in keeping the humerus in its socket. Assists in closing the
wing by drawing the humerus to the side of the body.
Intercostales (Fig. 24, No. 5). Location.—Between the ribs of the upper
thoracic region.
Origin and Insertion.—From the anterior border of one rib, the fibers,
passing obliquely upward and forward, and the lower portion downward
and forward, are inserted to the posterior border of the rib just in front.
Shape.—They are best developed in the anterior portion of the thoracic
region and extend down as far as the sternal ribs.
Relations.—Internally the pleura, and anteriorly and posteriorly the ribs.
Action.—The first rib being rendered fixed by the scalenus medius, the
muscles draw the ribs forward, thus aiding inspiration.
Levatores Costarum (Fig. 24, No. 2). Location.—Supero-lateral portion
of the thorax.
Origin and Insertion.—A series of muscles, the first of which extends
from the extremity of the transverse process of the twelfth vertebra, the
fibers passing downward and backward to the anterior free margin of the
upper third of the long posterior rib, and to the external surface close to its
margin. The others arise and insert in a similar manner from the ends of the
diapophyses of all the dorsal vertebræ and attach to each succeeding rib.
Those in front are best developed.
Shape.—Thin and triangular.
Relations.—External to the intercostales.
Action.—Aids in respiration.
Appendico-costales (Fig. 24, No. 1). Location.—The lateral side of the
thorax.
Origin and Insertion.—From the posterior edge of an uncinate process or
epineural appendage, the fibers extending downward and backward to the
outer surface of the succeeding rib.
Shape.—A series of thin triangular-shaped muscles.
Relations.—Internally, with the intercostales.
Action.—Aids in respiration.

Page 106

THE ANTERIOR PECTORAL GROUP

Tensor patagii longus
Tensor patagii brevis

Tensor Patagii Longus (Fig. 15C, No. 1; Fig. 14, No. 2). Location.—
Anterior shoulder region, in the triangular patagium of the wing.
Origin.—By a flat tendon common to it and the tensor patagii brevis
from the supero-mesial line of the head of the clavicle.
Insertion.—By a long slender tendon extending in the duplicature of the
patagium, with which the fibers blend. Passing to the side of the extensor
metacarpi radialis longus, it extends over the end of the radius and is
inserted to the os carpi radiale, and to the fascia which binds down the other
tendons on the anterior part of the wrist-joint.
Shape.—Cone-shaped belly terminating in a long tendon.
Relations.—Externally, with the skin; by its tendon, with the border of
the extensor metacarpi radialis longior.
Action.—Tenses the soft part in the fold of the wing, and aids in flexing
the forearm.
Tensor Patagii Brevis (Fig. 14, No. 3). Location.—In the triangular
patagium of the wing.
Origin.—From the head of the clavicle in common with the preceding.
Insertion.—The tendon bifurcates, one branch blending with the fascia of
the extensor metacarpi radialis longior, the other inserting just below the
tubercle on the external condyle of the humerus.
Shape.—Fleshy; somewhat broader and longer than the preceding.
Relations.—Interiorly, with the preceding.
Action.—Assists the tensor patagii longus in flexing the forearm.

THE PECTORAL MUSCLES

Pectoralis major
Pectoralis secundus
Pectoralis tertius

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Pectoralis Major (Fig. 13, No. 5). Location.—On the lateral side of the
sternum.
Origin.—From the posterior portion of the lateral wing of the sternal
body, from the outer marginal third of the keel of the sternum, and from the
entire outer side of the limb of the furcula or clavicle.
Insertion.—The fibers converging form toward the proximal third of the
humerus a broad tendon which by its insertion covers the entire palmar part
of the pectoral crest. A few of the tendinous fibers pass over the shoulder-
joint and blend with the long head of the biceps. Near this point it receives
the insertion of the dermo-humeralis.
Relations.—Interiorly, with the skin; superiorly, in the sternal region,
with the pectoralis secundus and the pectoralis tertius.
Shape.—Fleshy; largest of the pectorales.
Action.—Powerfully depresses the humerus. The chief muscle of flight.
Pectoralis Secundus (Fig. 13, No. 9; Fig. 15, No. A, 6). Location.—The
entire lateral side of the sternum.
Origin.—From the anterior sternal extremity of the lower third of the
coracoid, from the keel and sternal wing, and by a tendon from a
membraneous expansion between the coracoid and the clavicular bones and
from the lower third of the coracoid.
Insertion.—The fibers converge into a tendon, which passes upward
around the coracoid to its posterior through a canal formed by the scapula,
the coracoid, and the clavicle, the foramen triosseum (Fig. 15, No. A, 7).
This tendon then passes outward and downward, and becoming flat, inserts
to the humerus just anterior to the radial crest and nearer to the humeral
head than does the pectoralis major.
Relations.—Internally, with the breast-bone; externally, with the
pectoralis major; and superiorly, with the pectoralis tertius.
Shape.—Long, fusiform, fleshy.
Action.—Raises the wing.
Pectoralis Tertius (Fig. 13, No. 6; Fig. 15, No. A, 5). Location.—On the
antero-lateral side of the sternum.
Origin.—From the anterior half of the exterior of the body of the
sternum, from the fascia of the subclavius on the outer border of the costal

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process, and from the outer, lower third of the coracoid process.
Insertion.—The fibers pass upward to the outer side of the coracoid, and
becoming tendinous as they reach the humerus, by a strong flattened tendon
insert to the ulnar crest of the humerus on the proximal margin at about a
middle point of the pneumatic fossa.
Relations.—Externally, with the pectoralis major; interiorly, with the
pectoralis secundus; internally, with the fascia of the subclavius and the
sternum.
Shape.—Fleshy, fusiform.
Action.—Assists the pectoralis secundus in elevating the humerus.

MUSCLES OF THE SCAPULAR REGION

Coraco-humeralis
Scapulo-humeralis
Supraspinatus
Subclavius
Coraco-brachialis
Teres minor
Levator scapulæ
Thoraco-scapularis
Subscapularis

Coraco-humeralis. Location.—The scapulo-humeral region.
Origin.—From the outer side of the head of the coracoid, supero-laterally
to the long head of the biceps.
Insertion.—To the palmar part of the head of the humerus just inside of
the insertion of the pectoralis major.
Shape.—A delicate subcylindrical muscle.
Relations.—Superior to the head of the humerus.
Action.—Aids in extending the humerus.
Scapulo-humeralis (Fig. 14, No. 10). Location.—The scapulo-humeral
region.

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Origin.—From the inner side of the neck of the scapula just within the
head of the deltoid.
Insertion.—Passing over the top of the shoulder-joint it is inserted to the
palmar part of the humeral head between the insertion of the pectoralis
major and the pectoralis secundus.
Shape.—Narrow, flat ribbon.
Relations.—Along the upper margin of the larger portion of the deltoid.
Action.—Aids in extending the humerus.
Supraspinatus (Fig. 19, No. 22). Location.—Scapular region.
Origin.—From the superior surface and outer third of the scapula.
Insertion.—To the lower border of the pneumatic fossa of the humerus.
Shape.—Thin, flat, triangular.
Relations.—Externally, with the trapezius and posteriorly, with the teres
et infraspinatus.
Action.—If the scapula is the fixed point it will pull the humerus upward
and backward.
Subclavius. Location.—Anterior sternal region.
Origin.—From the entire outer surface of the sternal process of the
sternum and the adjacent outer surfaces of three or four of the
hemapophyses.
Insertion.—To the inferior margin of the coracoid bone, the longer fibers
passing over to the fossa in the lower third of the posterior part of the
coracoid.
Shape.—Rather small, fleshy.
Relations.—Overlapped by the pectoralis tertius.
Action.—Pulls the coracoid outward. Also aids in keeping the coracoid in
place.
Coraco-brachialis (Fig. 13, No. 15). Location.—Along the coracoid
shaft.
Origin.—By a delicate tendon from a small circular point on the postero-
mesial part of the shaft of the coracoid immediately above the attachment of
the subclavius and the fossa at that point.

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Insertion.—To the top of the ulnar tuberosity of the humerus. This
subcircular space is common to the teres minor and to this muscle.
Shape.—Long, fusiform.
Relations.—With the shaft of the coracoid between the teres minor and
subscapularis.
Action.—To depress the wing.
Teres Minor (Fig. 13, No. 14). Location.—The coraco-scapular region.
Origin.—From under the side of the anterior tip of the scapula.
Insertion.—Passing outward behind the coracoid head and beneath the
neck of the scapula, it is attached by a small tendon to the top of the ulnar
tuberosity of the humerus in common with the coraco-brachialis, with
which tendon it fuses.
Shape.—Small, chunky.
Relations.—Anteriorly, with the tip of the scapula and behind the
coracoid head. Posteriorly, with the coraco-brachialis.
Action.—Aids in the downward stroke of the wing.
Levator Scapulæ. Location.—Scapular region.
Origin.—By two strong digitations, one from each of the lateral
processes of the first cervical vertebra.
Insertion.—To the middle third of the inferior part of the blade of the
scapula.
Shape.—Small and flat.
Relations.—Inferior to the scapula.
Action.—Pulls the scapula forward, and with it the entire shoulder girdle,
which articulates like a hinge-joint at the costo-sternal juncture.
Thoraco-scapularis. Location.—Lateral side of the chest.
Origin.—From the outer part of the lower half of the first free rib, the
outer side of the next succeeding rib and its epineural appendage, and from
a similar surface on the next rib.
Insertion.—By a broad, flat tendon which passes between the two
divisions of the subscapularis and inserts at a point at the juncture of the
anterior and middle third of the outer margin of the scapula.
Shape.—Broad, flat.

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Relations.—Internally, with the ribs and the scapula.
Action.—When the scapula is fixed it is a muscle of inspiration. When
the ribs are fixed, it draws the scapula downward.
Subscapularis. Location.—Scapulo-humeral region.
Origin.—From the anterior and outer half of the scapula.
Insertion.—By a strong and subcylindrical tendon to the top of the ulnar
tuberosity of the humerus close to the combined tendons of the coraco-
brachialis and teres minor.
Shape.—A large and powerful muscle.
Relations.—The flat tendon of the thoraco-scapularis divides the
posterior portion of the belly into two portions.
Action.—A powerful rotary muscle of the head of the humerus; aids in
keeping the humeral head in the glenoid cavity.

THE MUSCLES OF THE BRACHIAL REGION

Biceps
Triceps
Deltoid
Brachialis anticus

Biceps (Fig. 13, No. 8). (Synonym.—Biceps brachii.)
Location.—The anterior brachial region.
Origin.—By a broad tendon it covers the top of the shoulder-joint,
dividing into two heads, giving rise to the long and the short heads. The
long is inserted into the outer part of the head of the coracoid just beyond
the glenoid cavity; the short head to the distal angle of the ulnar tuberosity
of the humerus.
Insertion.—To the ulna just in front of the articular cavity for the
trochlear surface of the distal extremity of the humerus.
Shape.—Large, subfusiform.
Relations.—On one side by the triceps and the other the deltoid and
anteriorly partially covered by the patagii muscles.

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Action.—A powerful flexor of the forearm.
Deltoid (Fig. 13, No. 12; Fig. 15, No. 8). Location.—Occupying the
lateral side of the humerus; the brachial region.
Origin.—Divided into two portions, the long narrow head extends from
the clavicular process of the scapula and from the adjacent surface of the
same bone. These fibers then extend around the back of the shoulder-joint,
and are joined by the fibers that arise from the entire outer surface of the
large os humero-scapulare. These latter fibers are inserted upon an
extensive area upon the anconal part of the bone beyond the humeral
articular head, and to almost the entire shaft below it.
Insertion.—By a subcylindrical tendon to the proximal side of the
tubercle of the external condyle, and above the insertion of the extensor
metacarpi radialis longus.
Shape.—Large, fleshy, with tendinous attachment.
Relations.—On one side by the biceps and the other by the triceps also
the patagii.
Action.—To extend the arm.
Triceps (Fig. 15, No. 7). (Synonym.—Triceps brachii.)
Location.—The posterior humeral region.
Origin.—By three portions: by the internal and external heads, and by the
long scapular head. The internal and the external heads are blended except
at their proximal extremities. Each head arises from the anconal surface of
the shaft of the humerus. The internal head being located toward the deltoid
attachment and the external head into the pneumatic fossa. The long head
extends from a circumscribed area just posterior to the glenoid cavity of the
scapula. The fibers pass around the shoulder-joint, beneath the deltoid.
Insertion.—The broad tendon passes over the elbow-joint and is inserted
to the entire under surface of the olecranon of the ulna.
Shape.—Long, large, fleshy.
Relations.—The supraspinatus passes between the internal and the
external heads. It is bounded by the biceps and the deltoid.
Action.—An extensor of the antibrachial region directly antagonizing the
biceps.

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Brachialis Anticus (Fig. 15, No. 9; Fig. 14, No. 5). Location.—In the
flexure of the humerus and the ulna.
Origin.—It arises fleshy from a circumscribed area on the inner side of
the anconal part of the distal extremity of the humerus.
Insertion.—The fibers passing directly over the elbow-joint become
inserted to the lateral surface of the proximal end of the ulna close to the
margin of the sigmoid cavity.
Shape.—Small, fleshy.
Relations.—With the joint.
Action.—Assists in flexing the forearm upon the arm. Protects the
structures in the anterior part of the elbow-joint.

THE MUSCLES OF THE FOREARM AND THE HAND

Extensor metacarpi radialis longior
Supinator brevis
Extensor digitorum communis
Pronator brevis
Flexor metacarpi radialis
Extensor ossis metacarpi pollicis
Pronator longus
Extensor indicis longus
Flexor digitorum sublimis
Flexor digitorum profundus
Flexor carpi ulnaris
Flexor carpi ulnaris brevior

Extensor Metacarpi Radialis Longior (Fig. 13, No. 17). Location.—
Superior to the radius.
Origin.—By two strong tendinous heads; the outer from the tubercle of
the external condyle of the humerus, just above the origin of the tendon of
the tensor patagii brevis; the inner and stronger portion from the tubercle
found above the oblique trochlear facet of the distal end of the radius.
Insertion.—Becoming a flat, broad, and strong tendon at about the
middle of the forearm, finally becomes inserted to the apex of the

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anchylosed first metacarpal of the carpo-metacarpus.
Shape.—A thick, fusiform belly, tendinous at both extremities.
Relations.—By the side of the pronator brevis.
Action.—Raises the hand, and draws it forward toward the radial margin
of the forearm and retains it on the same side.
Extensor Digitorum Communis (Fig. 15, No. 2). Location.—The upper
metacarpal region.
Origin.—Immediately below the tubercle of the external condyle of the
humerus.
Insertion.—By a small tendon to the outer side of the base of the pollex,
and at a mid-point upon the anterior rim of the proximal phalanx of the
middle finger.
Shape.—Small spindle-shaped, becoming tendinous at about the middle
of the forearm.
Relations.—Occupies the middle of the group of muscles on the outer
side of the forearm.
Action.—An extensor of the digit.
Supinator Brevis (Fig. 14, No. 7). Location.—The superior part of the
radius.
Origin.—From the external condyle of the humerus below the origin of
the tendon of the extensor digitorum communis.
Insertion.—To the outer side of the shaft of the radius, for nearly one-
third of its length.
Shape.—Thin, slender.
Relations.—Inferiorly, with the bone.
Action.—A supinator of the radial region, and antagonistic to the
pronators.
Flexor Metacarpi Radialis (Fig. 15, No. 10). Location.—The lowest of
the group of three muscles on the outer part of the forearm.
Origin.—By two tendinous heads, the longer from the external condyle
of the humerus, and the other just beyond the base of the olecranon.
Insertion.—Becomes tendinous at about the middle of the shaft of the
ulna and inserts to a prominent process on the proximal third of the

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posterior part of the shaft of the mid-metacarpal.
Shape.—Fusiform.
Relations.—Inferiorly, the anconeus and superiorly, the extensor
digitorum communis.
Action.—A powerful flexor of the hand.
Pronator Brevis (Fig. 13, No. 18). Location.—Supero-lateral side of the
forearm.
Origin.—From just above the internal condyle of the humerus.
Insertion.—The tendon passing obliquely across the interosseous space
and is inserted to the ulnar side of the shaft of the radius, just beyond the
juncture of the proximal and the middle thirds.
Shape.—Fusiform.
Relations.—Superior to the pronator longus.
Action.—Pronates the forearm, and flexes the forearm upon the arm.
Pronator Longus (Fig. 14, No. 6). Location.—Lateral side of the radio-
ulnar region.
Origin.—From the middle of the internal condyle of the humerus.
Insertion.—To the shaft of the radius just beneath the pronator brevis.
Shape.—Massive, ellipsoidal.
Relations.—Between the pronator brevis and flexor digitorum profundus.
Action.—A pronator.
Extensor Ossis Metacarpi Pollicis (Fig. 13, No. 23). Location.—
Slightly interposed between the ulna and radius.
Origin.—Immediately in front of the greater sigmoid cavity of the ulna.
Insertion.—To the palmar side of the base of the first metacarpal, in
common with the extensor metacarpi radialis longior.
Shape.—Delicate, straight.
Relations.—Superiorly, the extensor indicis longus, and inferiorly, the
anconeus and the flexor digitorum profundus.
Action.—Extends the hand upon the forearm.
Anconeus (Fig. 15, No. 4). Location.—Between the ulna and the radius.

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Origin.—By a short, strong, subcylindrical tendon from the lower
posterior of the external condyle of the humerus.
Insertion.—To the latero-radial side of the ulna somewhat beyond its
middle.
Shape.—Fusiform.
Relations.—Superiorly, the extensor indicis longus, and inferiorly, the
ulna.
Action.—A flexor of the forearm.
Extensor Indicis Longus (Fig. 13, No. 22; Fig. 15, No. 13). Location.—
Infero-lateral to the radius.
Origin.—From about one-half the surface of the proximal portion of the
radius.
Insertion.—Possesses a long tendon which passing over a groove at the
distal end of the ulna and receiving muscular fibers at the base of the
metacarpus, extends down the anterior part of the hand and is inclosed in a
sheath in front of the superior part of the first phalanx of the index-finger.
This tendon is inserted into the anterior upper rim of the distal phalanx.
Shape.—Small, thin.
Relations.—Supero-laterally with the radius.
Action.—Extensor of the digit.
Flexor Digitorum Sublimis. Location.—The forearm.
Origin.—From the internal condyle of the humerus.
Insertion.—Passing over the wrist, it is inserted to the middle phalanx of
the hand.
Shape.—A musculo-tendinous band, rather delicate and rudimentary.
Relations.—Closely adhering to the integument that stretches from the
internal condyle of the humerus to the wrist.
Action.—Assists these muscles. A flexor.
Flexor Digitorum Profundus (Fig. 13, No. 21). Location.—Lateral side
of the ulna.
Origin.—By two heads from the proximal extremity of the ulna, between
which the brachialis anticus passes.

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Insertion.—The two bellies uniting are attached to the under side of the
shaft of the ulna. It becomes tendinous about the middle of the shaft, and
inserts to the ulnar side of the base of the distal joint of the index-finger.
Shape.—A fleshy belly with long tendon.
Relations.—Inferiorly, with the flexor carpi ulnaris, superiorly, with the
pronator brevis.
Action.—A flexor of the digit.
Flexor Carpi Ulnaris (Fig. 13, No. 19). Location.—Inferior part of the
forearm.
Origin.—By two strong tendons; one from the side and posterior of the
internal condyle of the humerus, passing through the humero-ulnar pulley at
the side of the base of the olecranon process; the other, to the posterior of
the internal condyle of the humerus. It does not pass through a pulley.
Insertion.—A subcylindrical tendon extends back of the ulnare ossicle of
the carpus giving off a tendinous slip to the flexor digitorum profundus, and
becomes inserted to the anterior rim of the proximal phalanx of the index
digit. It has an attachment at the carpus.
Shape.—A strong fleshy belly terminating in a long tendon.
Relations.—The outermost inferior muscle of the forearm.
Action.—A powerful flexor of the hand upon the forearm.
Flexor Carpi Ulnaris Brevior (Fig. 13, No. 20). Location.—Inferior
part of the antibrachial region.
Origin.—From a broad area on the middle third of the upper side of the
shaft of the ulna.
Insertion.—Near the top of the outer edge of the anchylosed os magnum
of the carpo-metacarpus.
Shape.—Thin, somewhat flat.
Relations.—To the inside of the flexor digitorum profundus.
Action.—Flexes the hand upon the forearm and rotates the hand toward
the body.

OTHER MUSCLES OF THE DIGITS

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Extensor proprius pollicis
Flexor minimi digiti
Abductor minimi digiti
Interosseous palmaris
Flexor brevis pollicis
Flexor minimi digiti brevis
Interosseous dorsalis
Flexor metacarpi brevis

Extensor Proprius Pollicis (Fig. 13, No. 29a). Location.—Anterior to
the radio-carpal joint.
Origin.—From the ulnar side of the tendon of the extensor metacarpi
radialis longior.
Insertion.—To the antero-ulnar side of the pollex.
Shape.—Small, spindle-shaped; tendinous at both attachments.
Relations.—Inferiorly, with the proximal and anterior part of the
metacarpus.
Action.—An extensor of the pollex.
Flexor Brevis Pollicis (Fig. 13, No. 28a). Location.—Anterior to the
pollex.
Origin.—From the shaft of the mid-metacarpal bone, just below the
pollex.
Insertion.—Distal apex of the pollex.
Shape.—Short, small, fleshy.
Relations.—Superiorly, with the inferior part of the pollex.
Action.—Flexes the pollex.
Flexor Minimi Digiti. Location.—Inferior side of the metacarpus.
Origin.—From the posterior part of the median metacarpal close to the os
carpi ulnare. A few fibers extend to the ulna.
Insertion.—Into the base of the median phalanx.
Shape.—Small, slender, short.
Relations.—Superiorly, with the metacarpal bone.
Action.—A flexor of the digit.

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Flexor Minimi Digiti Brevis (Fig. 13, No. 30). Location.—Inferior to
the third, or small finger.
Origin.—From the lower and posterior end of the median metacarpal and
from the adjacent tendon of the preceding.
Insertion.—Inserted to the apex of the small finger.
Shape.—Small and rather rudimentary.
Relations.—Inferior to the small finger.
Action.—Acts as a posterior ligament of this joint.
Abductor Minimi Digiti. Location.—Supero-lateral side of the small
finger.
Origin.—From the proximal extremity of the anterior aspect of the third
finger.
Insertion.—To the posterior border of the proximal phalanx of the
second, or index-finger at a point just above the tip of the third finger.
Shape.—A few muscular fibers with some tendinous material.
Relations.—At the base of the median segment of the index-finger and to
the side of the third.
Action.—Antagonizes the powerful flexors on the back of the joint.
Interosseus Dorsalis (Fig. 13, No. 31). Location.—By the side of the
metacarpus.
Origin.—From the margin of the shaft of the median metacarpal.
Insertion.—To the anterior part of the base of the distal phalanx of the
index digit.
Shape.—Short, delicate, with long tendon.
Relations.—Internally, the metacarpal bone.
Action.—Extends the last bone of the middle finger.
Interosseus Palmaris (Fig. 13, No. 32). Location.—On the opposite side
of the bone from the interosseous dorsalis.
Origin.—From the shaft of the median metacarpal under the preceding.
Insertion.—To the apex of the last joint of the second, or middle finger.
Shape.—Small, delicate, with long slender tendon.
Relations.—Beneath the preceding and along the metacarpal bone.

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Action.—Flexes the terminal phalanx.
Flexor Metacarpi Brevis. Location.—To the lateral side of the
metacarpal bone.
Origin.—From the outer side of the distal extremity of the ulna.
Insertion.—To the base, in front, and on the ulnar side of the proximal
phalanx of the index digit.
Shape.—Delicate, with long slender tendon.
Relations.—On the lateral side of the ulna and the metacarpal bone.
Action.—Flexes the metacarpus.

MUSCLES OF THE POSTERIOR LIMB

Sartorius
Gluteus medius
Extensor femoris
Biceps flexor cruris
Semitendinosus accessorius
Femoro-caudal
Obturator internus
Abductor longus
Gluteus primus
Gluteus minimus
Vastus internus
Semitendinosus
Semimembranosus
Obturator externus
Gemellus
Adductor magnus

Sartorius (Fig. 23, No. 7). Location.—Extreme anterior portion of the
thigh.
Origin.—From the outer two-thirds of the superior surface of the raised
emarginations of the anterior border of the ilium, and by fascia from the
neural spines of the fourth dorsal vertebra.

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Insertion.—Obliquely by a semitendinous fascia to the inner edge of the
ligamentum patella, and to the inner and adjacent border of the anterior half
of the summit of the tibia.
Shape.—Large, fleshy.
Relations.—Posteriorly, with the gluteus primus and the vasti.
Action.—Extends the leg, flexes and adducts the thigh.
Gluteus Primus (Fig. 23, No. 8 and 9). Location.—The outer flat
massive muscle of the thigh.
Origin.—By a thin fascia from nearly the entire length of the supero-
internal margin of the pre-acetabular portion of the ilium, above the
antitrochanter, and from the entire length of the post-acetabular ridge.
Insertion.—Near the patella it joins the tendon of the extensor femoris,
and by aponeurosis spreads over the knee and is inserted to the crest of the
upper border of the tibia, the patella being incorporated in its aponeurotic
ligament.
Shape.—Triangular in shape, it is aponeurotic anteriorly and more fleshy
posteriorly.
Relations.—Anteriorly, covers over the posterior portion of the sartorius
and the body of the gluteus medius; posteriorly, bordered by the
semitendinosus and the biceps.
Action.—Abducts the thigh.
Gluteus Medius (Fig. 24, No. 11). Location.—Supero-anterior part of
the ilium under the gluteus primus.
Origin.—From the entire supero-internal margin of the pre-acetabular
surface of the ilium and the concave surface on the adjacent bone.
Insertion.—By a strong tendon which passes over a bursa on the anterior
rim of the trochanter and is inserted obliquely to this trochanter.
Shape.—A fleshy muscle filling the concavity of the pre-acetabular
division of the ilium.
Relations.—Superiorly, with the gluteus primus; inferiorly, with the
gluteus minimus.
Action.—Abducts and pulls the femur forward.
Gluteus Minimus (Fig. 24, No. 12). (Synonym.—Gluteus profundus.)

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Location.—Beneath the medius and the smaller of the two.
Origin.—To the anterior margin of the outer border of the ilium, and
from the supero-external surface of the last rib.
Insertion.—The fibers extending downward and backward and outward
become tendinous and are inserted below the trochanter of the outer part of
the upper third of the femur.
Shape.—Small, fleshy.
Relations.—Inferiorly, with the bone and superiorly, with the gluteus
medius.
Action.—Abducts and pulls the thigh forward.
Extensor Femoris (Fig. 24, No. 15). Location.—Anterior femoral
region. It is divided into two parts: the vastus externus and the crureus.
Origin.—The vastus extemus (Fig. 24, No. 14) arises tendinous from the
base of the trochanter of the outer part of the femur and from this point
down the bone approximately to the condyle. The crureus (Fig. 24, No. 13)
originates by a tendon from the anterior upper prominent rim of the
trochanter, from this point extending down the antero-external part of the
shaft of the femur.
Insertion.—Merges with the gluteus primus, and, by a fascia-like
arrangement, spreads over the front of the knee-joint inserts to the patella
and is also inserted into the crest of the tibia.
Shape.—Large, fleshy.
Relations.—Posteriorly, with the femur and anteriorly, with the sartorius.
Action.—Extends strongly the leg upon the thigh.
Vastus Internus (Fig. 16, No. 3). Location.—Internal and lateral side of
the femur.
Origin.—From the postero-internal part of the shaft of the femur just
below the head, and in a straight line extending down the femur.
Insertion.—By a broad tendon along the thickened inner border of the
summit of the tibia.
Shape.—Thick, long.
Relations.—Anteriorly, with the bone; surrounded by the other crural
muscles.

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Action.—Extends the leg upon the knee; a powerful assistant of the
extensor femoris.
Biceps Flexor Cruris (Fig. 17, No. D, 1). Location.—Posterior tibial
region.
Origin.—By a tendinous fascia from the post-acetabular ridge, extending
between the antitrochanter and the anterior point of the insertion of the
semitendinosus.
Insertion.—To the tuberosity on the external part of the shaft of the fibula
a short distance below the head.
Shape.—Large, rather cone-shaped with base directed upward.
Relations.—Anteriorly, with the vastus externus; posteriorly, with the
semitendinosus. The inferior tendinous portion passes through a tendinous
sling or pulley called the biceps band.
Action.—Flexes the leg upon the thigh.
Semitendinosus (Fig. 23, No. 10). Location.—Posterior femoral region.
Origin.—By a tough, strong fascia from the surface of the caudal
muscles and from the posterior third of the post-acetabular ridge.
Insertion.—The fibers pass downward and forward, and insert to the
tendinous raphe along the posterior margin of the semitendinosus
accessorius; lower down it merges with the median fascia of the inner head
of the gastrocnemius.
Shape.—Fleshy, broad, flat and long.
Relations.—Internally, with the semimembranosus and anteriorly, with
the biceps flexor cruris.
Action.—Flexes the leg.
Semitendinosus Accessorius. Location.—Posterior femoral region.
Origin.—From an oblique line just above the condyle, on the posterior of
the shaft of the femur.
Insertion.—Its fibers, passing upward and backward, attach themselves
to the tendinous raphe common to this muscle and the semitendinosus, and
are finally inserted to the inner side of the shaft of the tibia.
Shape.—Flat, oblong.

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Relations.—Posteriorly to the shaft of the femur, and externally to the
long adductors of the thigh.
Action.—Aids the preceding in flexing the leg.
Semimembranosus (Fig. 24, No. 17). Location.—Postero-internal to the
semitendinosus.
Origin.—From the outer surface of the ischium, beginning at the lower
margin of its notch on the posterior pelvic border, extends on a curved line
on the adjacent surface beyond.
Insertion.—The fibers, passing downward and forward, insert by a broad,
thin tendon to the shaft of the tibia a short distance below the head and on a
line parallel to the long axis of the tibia.
Shape.—Long, narrow, ribbon-shaped.
Relations.—Lies adjacent to the semitendinosus and in the same plane.
Action.—Directly flexes the leg.
Femoro-caudal (Fig. 24, No. 8). Location.—Infero-lateral to the caudal
and post-femoral region.
Origin.—By a delicate tendon from the base of the pygostyle.
Insertion.—By a thin, flat tendon upon the outer part of the shaft of the
femur below the trochanter and at about the juncture of the upper and
middle third of the bone.

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Fig. 24.—Second layer of muscles of
the thigh of a cock. Outside view. 1,
Appendico-costales. 2, Levatores
costarum. 3, Sacro-lumbalis. 4,
Longissimus dorsi. 5, Intercostales. 6,
Longissimus dorsi. 7, Latissimus dorsi.
8, Femoro-caudal. 9, Edge of obturator
externus. 11, Gluteus medius. 12,
Gluteus minimus. 13, Crureus. 14,
Vastus externus. 15, Extensor femoris.
16, Biceps flexor cruris. 17,
Semimembranosus. 18, Adductor
magnus. 19, Adductor longus. 20,
External abdominal oblique. 21,
Depressor coccygis. 22, Tibialis anticus.
23, Tibialis posticus. 24, Flexor
perforans digitorum profundus. 25,
Flexor perforatus medius secundus
pedis. 26, Flexor longus hallucis.

Shape.—Long, narrow, spindle-shaped, flattened from side to side.
Relations.—Interiorly to the obturator externus, and along the upper
border of the long adductors of the thigh and the semimembranosus.
Action.—Pulls the tail down and to one side.
Obturator Externus (Fig. 24, No. 9). Location.—External posterolateral
side of the pelvis.
Origin.—From the posterior half of the periphery of the ischiatic foramen
and the concavity found on the external surface of the lateral part of the
pelvis.

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Insertion.—The fibers pass across to the femur and are inserted by a
broad, flat tendon to the shaft of the femur just below the trochanter.
Shape.—Thick, fleshy.
Relations.—Lies just above the femoro-caudal muscle, the sciatic nerve
and femoral artery pass over and external to its tendon.
Action.—Pulls the head of the femur backward.
Obturator Internus (Fig. 16, No. E, 1). Location.—Occupies the space
between the ischium and the pubis.
Origin.—From the ventral surface of the ischium, including the posterior
border, from the inner line of the corresponding post-pubis, and from the
membrane covering the space between these two bones.
Insertion.—Becoming dense, subcylindrical, and strong, it passes
through the obturator foramen and is inserted to the outer part of the
trochanter of the femur, in common with the gemellus and opposite to the
insertion of the gluteus medius.
Shape.—Subtriangular and flat with a central tendon; bipenniform.
Relations.—Outside the pelvis the tendon lies upon the gemellus and is
external to it. Fills the obturator foramen and the space between the ischium
and the pubis.
Action.—Acts as a posterior stay to the head of the femur.
Gemellus (Fig. 25, No. 5). Location.—Posterior to the head of the femur.
Origin.—From the fossa between the acetabulum and the obturator
foramen, and on the outer side of the pelvis.
Insertion.—Its fibers are attached by fascia to the tendon of the obturator
internus, and pass directly to the trochanter of the femur where they insert
in common with that of the obturator internus.
Shape.—Strong, thick, chunky.
Relations.—Postero-external to the head of the femur.
Action.—Like the two preceding, when the head of the femur is fixed, it
pulls the pelvis forward and steadies it on the head of the femur.
Adductor Longus (Fig. 24, No. 19). Location.—In the posterior femoral
region.
Origin.—From a line on the lateral part of the pelvis.

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Insertion.—The fibers, passing downward and forward, are inserted on a
longitudinal line along the posterior part of the shaft of the femur.
Shape.—Broad, flat, fleshy.
Relations.—Posteriorly to the femur, and anteriorly to the adductor
magnus.
Action.—Adducts the thigh.
Adductor Magnus (Fig. 24, No. 18). Location.—Posterior femoral
region.
Origin.—From the fine constituting the lower boundary of the ischiatic
fossa on the outer lateral part of the pelvis.
Insertion.—The fibers pass downward and are inserted to the superior
curve of the internal femoral condyle. The internal head of the
gastrocnemius blends with this muscle just above its attachment.
Shape.—Long, narrow.
Relations.—Posteriorly to the adductor magnus and anteriorly to the
semimembranosus.
Action.—Strongly adducts the thigh.

THE TIBIAL GROUP

Gastrocnemius
Peroneus longus
Extensor longus digitorum
Tibialis posticus
Flexor longus hallucis
Flexor perforatus annularis primus pedis
Flexor perforatus medius secundus pedis
Flexor perforans digitorum profundus
Soleus
Tibialis anticus
Extensor hallucis brevis
Flexor perforatus indicis secundus pedis
Flexor perforatus medius primus pedis
Flexor perforatus indicis primus pedis

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Extensor brevis digitorum
Flexor hallucis brevis
Extensor annularis brevis
Gastrocnemius (Fig. 23, No. 11). Location.—Posterior tibial region.
Origin.—There are three heads: the internal, the external, and the tibial.
The external head extends by a short, flattened, strong tendon from the
postero-external part of the external condyle of the femur; the internal head
extends from the outer surface of the inner condyle of the femur; and the
tibial head extends from the entire inner rim of the tibial summit and from
the free edge of the adjacent crest.
Insertion.—At the lower fourth of the tibial shaft, terminates in a broad,
flat tendon which passes over the shallow, longitudinal groove of the tibial
cartilage, and, crossing the tibio-tarsal joint, is inserted to the posterior
surface of the hypotarsus of the metatarsal bone, and finally, below this
point, merges into the podothecal sheath confining the flexor tendons.
Shape.—Large, fleshy, somewhat cone-shaped with the base upward.
Relations.—The posterior fleshy muscle of the post-tibial region located
anterior to the soleus.
Action.—Extends the metatarsus on the tibia.
Soleus (Fig. 25, No. G, 1). Location.—The posterior tibial region.
Origin.—From the posterior part of the head of the tibia.
Insertion.—By a long slender tendon to the proximal end and toward the
inner angle of the tibial cartilage, some of the fibers passing to the tendon of
the gastrocnemius.
Shape.—Small, flattened.
Relations.—Anteriorly, with the flexor perforans digitorum profundus
and posteriorly, with the gastrocnemius.
Action.—Similar to that of the gastrocnemius.
Peroneus Longus (Fig. 23, No. 12). Location.—Antero-lateral tibial
region.
Origin.—From the raised crest in front of the head of the tibia, and from
the fascia that covers the outer side of the knee-joint.
Insertion.—The fibers, passing downward, then downward and outward,
terminate in a small tendon at the lower third of the tibia. This tendon

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bifurcates just above the tibial condyles at the outer part of the limb, the
shorter and stronger attaches to the fibrous fascia covering the tibial
cartilage, the other merging with the tendon of the flexor perforatus medius
primus pedis about 1 centimeter below the hypotarsus of the tarso-
metatarsus.
Relations.—Covers over all the muscles of the anterior tibial region.
Shape.—A broad muscular sheet.
Action.—Assists the flexor perforatus medius primus pedis.
Tibialis Anticus (Fig. 24, No. 22). Location.—In the anterior tibial
region.
Origin.—The muscular belly may be easily divided into two parts. The
inner head extends from the head of the tibia immediately beneath the
peroneus longus. The outer head arises by a strong tendon from a
depression on the antero-inferior ridge of the outer condyle of the femur.
Insertion.—The tendon passing through the fibrous ligamentous loop just
above the tibial condyles, inserts to a tubercle on the shaft just below the
head of the tarso-metatarsus.
Shape.—Large, fusiform.
Relations.—Beneath the peroneus longus.
Action.—Flexes the metatarsus upon the tibia.
Extensor Longus Digitorum (Fig. 25, No. G, 6). Location.—Anterior
tibial region.
Origin.—From the inferior portion of the crest and a portion of the shaft
of the fibula.
Insertion.—It becomes tendinous at the lower third of the bone, passing
under the bony ridge just above the condyle in front, and over the ankle-
joint. It is bound down by firm fascia, and at the trochlea of the basal toe
joints, divides into three small tendinous slips. These pass over the superior
part of the second, the third, and the fourth toes, bifurcating in their course,
and are inserted to the distal ones.
Shape.—Long, penniform, with a long, slender tendon.
Relations.—Immediately below the tibialis anticus.
Action.—Extends the digits as their long extensor.

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Extensor Hallucis Brevis (Fig. 25, No. G, 4). Location.—The anterior
metatarsal region, along the antero-internal edge.
Origin.—From just below the summit of the antero-internal part of the
head of the tarso-metatarsus, and from the adjacent shaft below, and from
the tendon of the tibialis anticus.
Insertion.—Into the process at the superior part of the bone of the bony
claw of the hallux.
Shape.—Slender, thin in diameter, with a long, slender tendon.
Relations.—Superiorly, with the antero-internal edge of the metatarsus
and interiorly, its tendon with the top of the hallux.
Action.—Extends the hallux.
Extensor Brevis Digitorum. Location.—On the anterior surface of the
metatarsus.

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Fig. 25.—Inner layer of muscles of the
thigh of a hen. Outside view.

A. Pad of fibrocartilage or meniscus of
femoro-tibial articulation. 1, Inner semi-
lunar fibrocartilage. 2, External semi-
lunar cartilage. 3, Anterior border.

B. Tarsal meniscus or pad of
fibrocartilage.

C. Articular surface of the tarsal joint. 1,
Posterior ligamentum cruciatum genu.
2, Femoral tendinous insertion of tibialis
anticus. 3, Ligamentum tibio-fibulare. 4,
Ligamentum interosseum. 5,
Ligamentum transversum of the
meniscus. 6, Anterior ligamentum
cruciatum genu.

D. 1, Tibia. 2, Fibula. 3, Femur. 4,
External ligamentum laterale genu.

E. Inferior surface of the tail of a hen. 1,
Infracoccygis. 2, Lateralis coccygis.

F. Outside pelvic view. 1, Obturator
ligament. 2, Tendon of the obturator
internus. 3, Ligamentum oblongum. 4,
Ligamentum capsulare. 5, Gemellus.

G. Outside view of leg of a cock. 1,
Soleus. 2, Flexor longus hallucis. 3,
Flexor perforans digitorum profundus.
4, Extensor brevis hallucis. 5, Extensor
brevis annularis. 6, Extensor longus

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digitorum. 7, Tendon of the tibialis
posticus.

H. 1, Transversalis abdominalis. 2,
Cotyloid cavity.

Origin.—By a small fleshy belly to the anterior part of the proximal end
of the metatarsus.
Insertion.—It becomes tendinous about the middle third of the
metatarsus. Extending down the anterior face of the metatarsus it is inserted
to the inner tubercle of the base of the first phalanx of the outer or fourth
toe.
Shape.—Long, slender.
Relations.—Posteriorly with the metatarsus.
Action.—Pulls the fourth toe upward and inward.
Flexor Hallucis Brevis. Location.—Postero-internal side of the
metatarsus.
Origin.—Side and lower margin of the inner aspect of the hypotarsus of
the tarso-metatarsus and from the shaft of this bone immediately below it.
Insertion.—Winds round inner side of basal joint of the hallux and is
inserted on its under side.
Shape.—Small flat muscle gradually tapering into a tendon.
Relations.—Posteriorly with the metatarsus.
Action.—To flex the hallux.
Extensor Annularis Brevis. Location.—On postero-external side of
metatarsus.
Origin.—External aspect of the hypotarsus and the shaft below.
Insertion.—Supero-external part of the basal phalanx of the fourth toe.
Shape.—Small flat muscle.
Relations.—Posteriorly with the metatarsus.
Action.—Extensor of the fourth toe.
Tibialis Posticus (Fig. 24, No. 23). Location.—In the posterior tibial
region.

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Origin.—From the whole shaft of the fibula below the insertion of the
biceps flexor cruris, and from the shaft of the tibia a short distance below
this insertion. Also from the interosseous membrane, and the adjacent
surface of the tibial shaft.
Insertion.—Passing in front of the external malleolus, crossing the ankle-
joint, finally inserted into the outer edge of the summit of the tarso-
metatarsal bone.
Shape.—Long, subcylindrical.
Relations.—Medially, with the flexor perforans digitorum pedis;
superiorly, with the postero-external portion of the tibia.
Action.—Extends the metatarsus upon the tibia.
Flexor Perforatus Indicis Secundus Pedis (Fig. 17, No. 5). Location.—
The posterior tibial region.
Origin.—From the external surface of the outer condyle of the femur, just
below the head of the gastrocnemius.
Insertion.—Passing in an oblique manner along posterior to the tibia,
extends through the superficial part of the tibial cartilage to the outer side of
the leg; then crossing the tibio-tarsal joint, it passes through a special canal
of the hypotarsus, down the back of the tarso-metatarsus, under the annular
ligament of the sole of the foot and a cartilaginous structure below this
ligament, over the trochlea, and is inserted to the middle shaft of the second
phalanx of the second toe.
Shape.—Thin, flat, broadly spindle-shaped.
Relations.—Posteriorly, with the flexor perforatus medius secundus
pedis, and anteriorly, with the flexor perforatus annularis primus pedis.
Action.—Flexes the toes.
Flexor Longus Hallucis (Fig. 17, No. 7; Fig. 25, No. 2). Location.—The
posterior tibial region.
Origin.—By two tendinous heads: one from the posterior part of the
femur, just below the two condyles; the other from the outer part of the
external condyle of the femur. The deep flexor passes between these two
heads.
Insertion.—Becoming tendinous at the lower third of the leg, passes
beneath the superficial flexors in a special canal on the outer side of the

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tibial cartilage, and extends through the large canal of the hypotarsus (Fig.
12, No. F, 5) next to the shaft, then down to the apex of the accessory
metacarpal bone. It is inserted to the tubercle on the inferior proximal end
of the ungual phalanx.
Shape.—Large, fusiform.
Relations.—With the exterior of the deep flexors.
Action.—Flexes the hallux as its long flexor.
Flexor Perforatus Annularis Primus Pedis (Fig. 17, Nos. D, 8 and C,
6). Location.—The posterior tibial region.
Origin.—From the inner side of the belly of the flexor longus hallucis.
Insertion.—Becoming tendinous at the lower third of the tibia, passes a
little to the outer side and through the tibial cartilage, then over the ankle-
joint and through the hypotarsal canal (Fig. 12, No. 5) to the under side of
the outer toe, where it forms a sheath through which the deep flexors
extend. It gives off on either side a tendinous slip which attaches to the
basal phalanx.
Shape.—Long, slender, compressed laterally.
Relations.—Internally, with the flexor perforatus indicis secundus pedis,
and externally, with the flexor longus hallucis.
Action.—Flexes the toes as their long flexor. A second flexor of the outer
toe.
Flexor Perforatus Medius Secundus Pedis (Fig. 17, No. 9). Location.
—The posterior tibial region.
Origin.—From a strong fascia that merges with the knee-joint, and by a
tendon from the external condyle of the femur in common with the tendon
of the flexor perforatus indicis secundus pedis.
Insertion.—Continued as a flattened tendon extending from the lower
third of the leg, passing obliquely through the tibial cartilage and then
through the interno-posterior canal of the hypotarsus, (Fig. 12, No. F, 5)
inserted to the second joint of the middle toe.
Shape.—Long, fusiform.
Relations.—With the shaft of the fibula, which it covers.
Action.—Flexes the middle toe.

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Flexor Perforatus Medius Primus Pedis (Fig. 17, No. 2). Location.—
Posterior tibial region.
Origin.—From the inner side of the muscular portion of the flexor
perforatus annularis primus pedis.
Insertion.—Terminating in a flattened tendon, passes through the tibial
cartilage and hypotarsus, and then extends along the shaft of the basal joint
of the third toe, and, dividing into two slips, inserts to either side of its
shaft.
Shape.—Long, rather small.
Relations.—With the flexor perforatus annularis primus pedis on the
inner side.
Action.—Flexes the third toe.
Flexor Perforatus Indicis Primus Pedis (Fig. 17, No. 4). Location.—
The posterior tibial region.
Origin.—From a thin, broad tendon, on the external condyle of the
femur, in common with the flexor perforatus medius secundus pedis.
Insertion.—Becoming tendinous, passes through the tibial cartilage and
the hypotarsus of the metatarsus (Fig. 16, A) and inserts to the sides of the
basal joint of the second toe.
Shape.—Long, slender, fusiform; somewhat flattened laterally.
Relations.—With the flexor perforatus medius secundis pedis,
posteriorly.
Action.—A flexor of the toes.
Flexor Perforans Digitorum Profundus (Fig. 24, No. 24 and Fig. 25,
No. G, 3). Location.—The posterior tibial region.
Origin.—From the posterior part of the external condyle of the femur,
from the posterior part of the tibia just below the summit, and from a point
near the origin of the soleus.
Insertion.—Its heavy flattened tendon passes through the tibial cartilage,
this tendon dividing, the branches pass along the under side of the toes,
perforating the outer tendons and become inserted to the proximal tubercle
at the base of the under side of the ungual phalanxes of the second, third,
and fourth toes.
Shape.—Long, fleshy, with a long tendon.

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Relations.—Closely with the tibial bone; the deepest of all the flexors.
Action.—Flexes the digits.

THE MUSCLES OF THE EYE

Orbicularis palpebrarum
Depressor palpebræ inferioris
Pyramidalis nictitans
Obliquus inferior
Rectus inferior
Levator palpebræ superioris
Quadratus nictitans
Obliquus superior
Rectus superior
Rectus externus
Rectus internus

Orbicularis Palpebrarum (Fig. 7, No. 30). (Synonym.—Orbicularis
oculi.)
Location.—Upon the lacrimal and maxillary bones.
Origin.—From the lacrimal and maxillary bones and the ciliary margin.
Insertion.—To the lower free edge of the tarsal cartilage.
Shape.—Thin, delicate layer of fibers.
Relations.—Externally, with the skin; internally, with the lacrimal and the
maxillary bones.
Action.—Aids in closing the eye.
Levator Palpebræ Superioris (Fig. 7, No. 24). Location.—Along the
superior roof of the orbit.
Origin.—Along a longitudinal line found near the middle of the roof of
the orbit.
Insertion.—To the ciliary margin of the upper lid, near the outer canthus.
Shape.—Thin, delicate layer.
Relations.—Superiorly, with the bony wall, and inferiorly, with the
eyeball.

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Action.—Raises the superior eyelid.
Depressor Palpebræ Inferioris (Fig. 7, No. 29). (Synonym.—Malaris.)
Location.—Along the inferior border of the eye.
Origin.—From the inferior border of the interorbital foramen.
Insertion.—To the lower lid.
Shape.—Thin, flat, delicate.
Relations.—Superiorly, with the eyeball; inferiorly, with the inferior
orbital wall.
Action.—Pulls the lower lid down.
Quadratus Nictitans (Fig. 26, No. B, 7). Location.—Above the eyeball
along the inferior border of the upper wall of the orbit.
Origin.—From the sclerotic from the upper part of the ball.
Insertion.—To the upper part of the sheath of the optic nerve near the
optic foramen.
Shape.—Broad, thin, quadrate.
Relations.—Inferiorly, with the eyeball; superiorly, with the orbital wall,
with the superior oblique, and with the superior rectus.
Action.—Aids in pulling the nictitating membrane obliquely outward and
downward over the forepart of the eyeball.
Pyramidalis Nictitans (Fig. 26, No. B, 8). Location.—Inferoposteriorly
to the eyeball.
Origin.—From the lower nasal side of the eyeball.
Insertion.—The fibers converge toward the upper part of the optic nerve,
into a tendon which passes through a pulley at the free margin of the
quadratus. Inserts to the lower part of the margin of the third eyelid, the
nictitans.
Shape.—Pyramidal; of thin layers of fibers.
Relations.—Internally, with the bony orbital wall; externally, with the
eyeball.
Action.—Aids the quadratus nictitans.
Obliquus Superior (Fig. 26, No. B, 5). (Synonym.—Obliquus dorsalis.)
Location.—Superior to the eyeball.

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Fig. 26.—Structures of the eye and
nasal passage.

A. 1, The anterior turbinated bone. 2,
The posterior turbinated bones. 3,
Orbital gland. 4, Ophthalmic division of
the fifth pair of cranial nerves. 5,
Section through the cerebrum. 6,
Section through the skull showing the
air spaces. 7, Section through the comb.
8, Anterior portion of the upper beak. 9,
Edge of the hard palate.

B. The intrinsic muscles of the eyeball.
1, Superior rectus. 2, Internal rectus. 3,
Inferior rectus. 4, External rectus. 5,
Superior oblique. 6, Inferior oblique. 7,
Quadratus. 8, Pyramidalis. 9, Optic
nerve. 10, Edge of membrana nictitans.

C. Posterior part of the eye showing at
the inferior portion of the ball the
pyramidalis muscle at 1, and at 2, the
quadratus. 3, Optic nerve.

D. Inner view of the posterior part of the
vitreous chamber. 1, Sclerotic coat. 2,
Choroid coat. 3, Retina. 4, Pecten.

E. Longitudinal section through the eye
of a hen. 1, Cornea. 2, Anterior
chamber. 3, Scleral ring. 4, Crystalline
lense. 5, Iris. 6, Retina. 7, Sclerotic. 8,
Choroid. 9, Pecten. 10, Optic nerve. 11,

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Vitreous chamber.

F. An edge view of the crystalline lense
of a hen showing it to be asymmetrical
biconvex. 1, The anterior side. 2, The
posterior side.

G. The upper section through the
anterior portion of the anterior
turbinated bone showing one complete
circle and the lower a section through
the middle turbinated showing one and
one-half turns.

Origin.—From the orbital septum just back of the inner canthus, the
fibers passing backward and forward.
Insertion.—Into the sclera, anterior to the sclerotic plates.
Shape.—Small, thin, fan-shaped.
Relations.—With the eyeball, superiorly; at its extremities with the
superior rectus, interiorly.
Action.—Rotates the eyeball.
Obliquus Inferior (Fig. 26, No. B, 6). (Synonym.—Obliquus ventralis.)
Location.—Inferior to the eyeball.
Origin.—From the interorbital septum near the inner canthus of the eye.
Insertion.—By a broad expansion to the inferior portion of the eyeball.
Shape.—Tendinous at its insertions; fan-shaped as it passes downward
and outward.
Relations.—Internally, with the eyeball; and externally, with the bony
orbital wall, with the inferior rectus muscle, inferiorly.
Action.—Aids in rotating the eye; opposes the obliquus superior.
Rectus Superior (Fig. 26, No. B, 1). (Synonym.—Rectus dorsalis.)
Location.—Superior to the eyeball.
Origin.—Along the supero-posterior border of the optic foramen.
Insertion.—To the sclera just within the margin of the bony circle of the
eye.
Shape.—Flat, thin.

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Relations.—Internally, with the obliquus superior; superiorly, with the
bony wall of the orbit.
Action.—To pull the eyeball upward.
Rectus Inferior (Fig. 26, No. B, 3). (Synonym.—Rectus ventralis.)
Location.—Inferior to the eyeball.
Origin.—From the inferior border of the optic foramen.
Insertion.—To the lower portion of the eyeball within the margin of the
bony circle of the eye.
Shape.—Thin, fan-shaped.
Relations.—Superiorly, with the eyeball; inferiorly, with the bony wall of
the orbit.
Action.—Pulls the eyeball downward.
Rectus Externus (Fig. 26, No. B, 4). (Synonym.—Rectus lateralis.)
Location.—External to the eyeball.
Origin.—By two heads infero-laterally to the optic foramen.
Insertion.—To the postero-external side of the eyeball.
Shape.—Short, fan-shaped.
Relations.—Internally, with the eyeball; externally, with the bony wall of
the orbit.
Action.—Pulls the eyeball outward.
Rectus Internus (Fig. 26, No. B, 2). (Synonym.—Rectus medialis.)
Location.—Inner side of the eyeball.
Origin.—From the supero-anterior border of the optic foramen.
Insertion.—To the sclera on the anterior portion of the eyeball.
Shape.—Thin, fan-shaped.
Relations.—Internally, with the eyeball and with the pyramidalis;
externally, with the bony wall of the orbit.
Action.—Pulls the eyeball inward.

THE MUSCLES OF THE EAR

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Circumconcha
Tensor tympani

Circumconcha (Fig. 7, No. 32). Location.—Surrounds the external ear.
Origin and Insertion.—The circumconcha, surrounding the periphery of
the ear, is adherent to the skull and loosely to the skin, and is attached to the
outer terminus of the supra-occipital crest.
Relations.—Internally, with the skull; externally, with the skin.
Action.—Relaxes the tympanum.
Tensor Tympani (Fig. 7, No. 31). Location.—External to the quadrate
and to the external auditory meatus.
Origin and Insertion.—From the surface of the quadrate and the inner
end of the quadrato-jugal to the inner surface of the tympanum.
Shape.—A few fibers.
Relations.—Internally, with the quadrate and the quadrato-jugal;
externally, the integumental duplicature.
Action.—Tenses the tympanum.

FUNCTIONS OF MUSCLES

To cause the feathers on the top of the head to lie flat:
Dermo-frontalis.
To raise the feathers along the superior part of the neck and along the
dorsal region:
Dermo-dorsalis.
To tense the patagial region:
Dermo-tensor patagii,
Dermo-temporalis.
To cause the feathers to lie close to the body:
Dermo-humeralis,
Dermo-pectoralis.
To tense the lateral cervical integument:
Dermo-temporalis.
To support the lingual apparatus and superior larynx:
Platysma myoides.

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To manipulate the feathers and skin of the inferior part of the neck:
Cleido-trachealis.
To control the skin in the shoulder region:
Dermo-spinalis.
To cause the feathers of the back to lie close to the skin:
Dermo-iliacus.
To depress the humeral region:
Dermo-ulnaris.
To close the jaw:
Temporalis,
Pterygoideus internus,
Pterygoideus externus,
Masseter.
To open the jaw:
Biventer maxilla,
Entotympanic.
To raise the trachea and hyoid apparatus:
Digastricus.
To elevate the tongue:
Mylo-hyoideus.
To pull the tongue to one side:
Singly[5]—
Cerato-hyoideus,
Stylo-hyoideus.
Alone when the larynx is fixed—
Sterno-hyoideus.
Those which protrude the tongue from the mouth:
Together—
Cerato-hyoideus,
Genio-hyoideus.
To aid in deglutition:
When the base of the tongue is fixed—
Sterno-hyoideus.
To depress the tongue:
Together—
Sterno-hyoideus.
To depress the tip of the tongue and elevate the base:

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Depressor glottis.
To elevate the hyoid arches:
Cerato-glossus.
To extend the head:
Complexus,
Rectus capitis anticus minor.
To flex the head upon the neck:
Flexor capitis inferior.
To extend the head on the neck and elevate the neck:
Biventer cervicis.
To raise the neck upward:
Longus colli posticus.
To flex each vertebra on the preceding or succeeding laterally:
Obliquus colli,
Intertransversales.
To pull the neck downward:
Longus colli anterior.
To pull the head downward:
Together—
Rectus capitis lateralis,
Trachelo-mastoideus.
To pull the head downward and to one side:
Singly—
Rectus capitis lateralis,
Trachelo-mastoideus.
To approximate the spinous processes of the vertebræ:
Interspinales.
To approximate the vertebræ in a supero-lateral direction:
Interarticulares.
To flex the vertebræ supero-laterally:
Obliquo-transversales.
To extend the neck:
Together when the first rib is fixed—
Scalenus medius.
To close the glottis:
Constrictor glottidis.
To open the glottis:

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Thyreo-arytenoideus.
To approximate the tracheal rings:
Tracheo-lateralis.
To tense the inferior larynx:
Broncho-trachealis posticus,
Broncho-trachealis anticus,
Broncho-trachealis brevis,
Bronchialis posticus,
Bronchialis anticus.
To relax the inferior larynx:
Sterno-trachealis.
To aid in respiration:
When the first rib is fixed—
Intercostales.
When wing is fixed—
Latissimus dorsi,
Dermo-cleido dorsalis.
When the scapula is fixed—
Serratus magnus anticus,
Serratus parvus anticus,
Thoraco-scapularis,
Levatores costarum,
Appendico-costales,
Triangularis sterni.
To flex the shoulder-joint:
Latissimus dorsi.
To elevate the humerus:
Latissimus dorsi.
To draw the scapula forward:
Trapezius,
Rhomboideus.
To close the wing:
Teres et infraspinatus.
To extend the humerus:
Coraco-humeralis,
Scapulo-humeralis.
To pull the humerus upward and backward:

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When the scapula is fixed—
Supraspinatus.
To pull the coracoid outward:
Subclavius.
To depress the wing:
Coraco-brachialis.
To depress the scapula:
When the ribs are fixed—
Thoraco-scapularis.
To rotate the humerus:
Subscapularis.
To flex the forearm:
Pronator brevis,
Biceps,
Brachialis anticus,
Anconeus,
Tensor patagii longus,
Tensor patagii brevis.
To extend the arm:
Deltoid.
To extend the antibrachial region:
Triceps.
To raise and to draw the hand forward:
Extensor metacarpi radialis longior.
To extend the digit:
Extensor indicis longus,
Extensor digitorum communis,
Extensor proprius pollicis,
Interosseous dorsalis.
To supinate the radial region:
Supinator brevis.
To flex the hand:
Flexor metacarpi radialis.
To pronate the forearm:
Pronator brevis,
Pronator longus.
To extend the hand on the forearm:

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Extensor ossis metacarpi pollicis.
To flex the digit:
Flexor minimi digiti,
Flexor digitorum sublimis,
Flexor brevis pollicis,
Flexor digitorum profundus,
Interosseous palmaris.
To flex the hand upon the forearm:
Flexor carpi ulnaris,
Flexor carpi ulnaris brevior.
To rotate the hand toward the body:
Flexor carpi ulnaris brevior.
To abduct the digits:
Abductor minimi digiti.
To flex the metacarpus:
Flexor metacarpi brevis.
To extend the leg:
Sartorius.
To adduct the thigh:
Sartorius,
Adductor longus,
Adductor magnus.
To abduct the thigh:
Gluteus primus,
Gluteus medius,
Gluteus minimus.
To pull the thigh forward:
Gluteus minimus,
Gluteus medius.
To extend the leg upon the thigh:
Extensor femoris,
Vastus internus.
To extend the leg upon the knee:
Vastus internus.
To flex the leg upon the thigh:
Biceps flexor cruris,
Semitendinosus,

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Semitendinosus accessorius,
Semimembranosus.
To pull the tail down and to one side:
Femoro-caudal.
To pull the head of the femur backward:
Obturator externus.
To act as a posterior stay to the head of the femur:
Obturator internus.
To pull the pelvis forward and to steady it on the head of the femur:
Gemellus,
Obturator internus,
Obturator externus.
To extend the metatarsus on the tibia:
Gastrocnemius,
Soleus,
Tibialis posticus.
To flex the toes:
Peroneus longus,
Flexor perforatus medius primus pedis,
Flexor perforatus indicis secundus pedis,
Flexor perforatus medius secundus pedis,
Flexor perforatus indicis primus pedis,
Flexor perforans digitorum profundus,
Flexor longus hallucis,
Flexor perforatus annularis primus pedis.
To flex the metatarsus on the tibia:
Tibialis anticus.
To extend the toes:
Extensor longus digitorum,
Extensor hallucis brevis.
To flex the back laterally and to aid in raising the body.
Sacro-lumbalis,
Longissimus dorsi.
To elevate the tail:
Levator coccygis,
Levator caudæ.
To depress the tail:

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Depressor caudæ,
Infracoccygis.
Together—
Depressor coccygis,
Lateralis caudæ.
To pull the tail downward and to one side:
Singly—
Lateralis coccygis.
Depressor coccygis,
Lateralis caudæ.
To close the eyelids:
Orbicularis palpebrarum.
To raise the superior eyelid:
Levator palpebræ superioris.
To pull the lower eyelid downward:
Depressor palpebræ inferioris.
To pull the membrana nictitans over the eyeball:
Quadratus nictitans,
Pyramidalis nictitans.
To rotate the eyeball:
Obliquus superior,
Obliquus inferior.
To pull the eyeball upward:
Rectus superior.
To pull the eyeball downward:
Rectus inferior.
To pull the eyeball outward:
Rectus externus.
To pull the eyeball inward:
Rectus internus.
To tense the ear drum:
Tensor tympani.
To relax the ear drum:
Circumconcha.
To depress the humerus:
Pectoralis major.
To raise the humerus:

Page 149

Pectoralis secundus,
Pectoralis tertius.
5. Muscles are arranged in pairs. Singly means one muscle acting alone, i.e., without its fellow;
together means acting both at the same time.

Page 150

SPLANCHNOLOGY

The Digestive Apparatus.—This apparatus, apparatus digestorius,
consists of the organs directly concerned in the reception of food, in its
passage through the body, and in the expulsion of the unabsorbed portion.
For convenience, these organs are grouped as follows: the alimentary canal
and the accessory organs.
The alimentary canal is a tube which extends from the mouth to the anus.
It has a complete lining of mucous membrane, external to which is an
almost continuous muscular coat. The abdominal portion of the tube is
largely covered with a serous membrane, the visceral peritoneum. The canal
consists of the following consecutive segments: mouth, pharynx, first
portion of the esophagus, crop, second portion of the esophagus,
proventriculus, gizzard, small intestine, large intestine, and cloaca.
The accessory organs are beak, tongue, salivary glands, liver, and
pancreas.
The Mouth (Fig. 27).—The distinctive character of the mouth of the
fowl consists, in the absence of lips and teeth and instead of jaw bones of
other animals, of a beak. The edge of the beak is covered by a horn-like
gum. The shape of the beak differs in the various classes of birds. In the
chicken the beak is short, strong, thick, and pointed; in palmipeds it is
flattened. The upper mandible extends out over the lower mandible. The
outer portion of the upper and the lower beaks is covered by a horny sheath.
There is no velum, and the mouth cavity is extended rather continuously
into the pharynx (Fig. 27, No. 4). The posterior cross bar of the hard palate
(Fig. 27, No. 5), which possesses a row of filiform papillæ projecting
backward, marks the upper boundary line of the mouth; while the posterior
end of the tongue (Fig. 27, No. 6), likewise with a row of filiform papillæ,
marks its lower boundary line.

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Parts of the Mouth.—The mouth of fowls is divided into an upper and a
lower half. The upper half is divided into an anterior and a posterior part.
The anterior part extends from the anterior tip of the beak to the posterior
nares. It is further divided into an outer hard part and an inner soft part. The
outer part is covered by epithelium which may be considered as a
continuation from the upper outer portion of the beak. A portion of this is
cornified. The inner part is covered by a mucous membrane containing
mucous glands, nerves, and blood-vessels.
In the posterior part of the upper half of the mouth, are situated the
posterior nares (Fig. 27, No. 10) which appear as a longitudinal slit in the
center of the hard palate. There is also found in this part a furrow which
contains the opening of the Eustachian tubes, or tubæ auditivæ. There are
also two ridges near the same posterior part in which are red and white
papillæ, which may appear in rows, and which contain mucous glands.

Fig. 27.—Mouth and pharynx of a cock
laid open. 1, Eye. 2, Edge of beak
covered with a horn-like gum. 3,
Tongue. 4, Pharynx. 5, Posterior cross
bar of hard palate. 6, Posterior end of
tongue. 7, Anterior end of esophagus. 8,
Phrenum. 9, Palatal papillaries. 10,
Posterior nares.

The lower half of the mouth lies between the lower jaw bones and the
walls of the mouth cavity. The tongue is attached here by means of the
phrenum (Fig. 27, No. 8). This half of the mouth forms a pocket-like
structure which aids in taking up the food.

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The mouth cavity is lined with stratified squamous epithelium,
continuous with that of the pharynx and the esophagus. Taste buds are
located in the mucous membrane of the mouth.

Fig. 28.—Various anatomical parts of the fowl.

C. A section through the nasal region of the fowl. 1, Nasal passages showing the
turbinated bones dividing the nasal passage into the superior, middle and inferior
meati. 2, The infraorbital sinus. 3, The hard palate.

D. Herbst’s touch corpuscle from the beak of a quail.

E. A vertical section through the ductus cochlearis of a pigeon. 1, A blood-vessel.
2, The periosteum. 3, The bony structure. 4, The vascular integument. 5. The
scala vestibuli. 6, The inner hyaline cylindrical cells. 7, The membrana tectoria.
8, The papilla acustica basilaris. 9, The membrana basilaris. 10, The scala
tympani. 11, The ganglion of the cochlear nerve in the ramus basilaris. 12, The
periosteum (Gadow).

F. A corpuscle of the soft papilla of a duck’s tongue.

J. A transverse section through a feather papilla. 1, The pulp. 2, The malpighian
layer. 3, The corium. 4, The stratum corneum of the papilla. 5, The malpighian
cell group of the main shaft. 6, The horny sheath.

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In many water fowls, as geese and ducks, the gum edge of the mandible
has grooves extending crosswise, in which are numerous terminals of the
trigeminus nerve arranged as taste organs (Fig. 29, G and Fig. 28, D and F).
In many birds of prey and in water birds, e.g., the goose and the duck, there
is found at the base of the beak, a very thin, nervous or sensitive skin, waxy
in appearance, called the ceroma.

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Fig. 29.—Various anatomical parts of
the fowl.

A. 1, The superior semicircular canal. 2,
The vestibular nerve. 3, The meatus
auditorius internus—the entrance of the
auditory nerve. 4, The entrance of the
cochlear nerve. 5, Posterior semicircular
canal. 6, The ampulla.

B. Side papilla of the tongue. 1 and 2,
Papillæ showing a fibrous central core
supporting blood-vessels and nerves. 3,
The basement membrane consisting of
connective tissue.

G. Herbst’s corpuscle of the tongue of a
duck, showing the capsule, lamella and
around the nerve zone, numerous round
bodies arranged in two rows.

H. From the cristæ acoustica of the
ampulla of the dove. A, A vertical

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section with isolated fiber cells. 1 and 2,
The nerve fibers. 3, The hair cells.

I. A longitudinal section through a
feather papilla showing a young feather.
1, The developing feather. 2, The horny
sheath. 3, The epithelium. 4, Stratum
corneum. 5, Stratum malpighi. 6,
Corium. 7, Malpighian cell group of the
follicle.

The Hard Palate.—The hard palate, palatum durum, forming the roof of
the mouth has for its boundaries the beak anteriorly, the mandibular arches
laterally, and the pharynx posteriorly. It has four or five transverse bars,
projecting posteriorly from each of which is a row of filiform papillæ (Figs.
27 and 29).

Fig. 30.—A section through the wall of
the crop of a hen. 1, The outer muscular
layer showing longitudinal fibers. 2, The
inner muscular layer showing the
sectioned ends of the bundles of muscle
fibers. 3, Stratified squamous
epithelium. 4, The outer surface or
lumen of a fold. 5, The stroma,
muscularis mucosa, and submucosa.

The beak (Fig. 4, No. 1) with little if any aid from the tongue, is the
prehensile organ.

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The Tongue (Fig. 27, No. 3). Location.—The tongue (lingua) of the fowl
is situated in the floor of the mouth between the rami of the lower mandible,
and is slung to the cranium by the cerato-branchial element of the os
hyoideum (Fig. 18, No. 2).
Shape.—The tongue, is pointed in front and wide behind, shaped like an
Indian arrow-head, and is supported by the bony and cartilaginous hyoid
apparatus (Fig. 9, A).

Fig. 31.—The visceral organs of the
hen. 1, Tongue. 2, Larynx. 3, Glottis. 4,
First portion of the esophagus. 5, Crop.
6, Second portion of the esophagus. 7,
Proventriculus. 8, Duodenum. 9, Free or
floating portion of the small intestine.
10, Mesentery supporting the free
portion of the small intestine. 11, Cæca.
12, Rectum or large intestine. 13,
Cloaca. 14, Anus. 15, Liver. 16, Gall-
bladder. 17, Pancreas. 18, Gizzard. 19,
Trachea. 20, Lungs. 21, Spleen.

Structure.—The free part of the tongue consists of two long tubes which
are formed by the rolling in of the ventral sides of its horny coverings. The
dorsal plate, which constitutes one-half of the horny sheath, does not form
a part of the tubes, but ends in the region of the point of the entoglossum.

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The top surface is covered by a thick stratum corneum, giving it a rather
horny surface. Glands occur in the posterior part of the tongue.
While not so freely movable as in mammals, the tongues of birds are
very flexible.
The Pharynx (Fig. 27). Location.—The anterior part of the pharynx
joins with the mouth and the posterior part with the upper portion of the
esophagus and the superior larynx. The pharynx is bounded anteriorly by
the base of the tongue and by the posterior edge of the hard palate.
Posteriorly, it is marked by the entrance of the esophagus and by a ridge of
filiform papillæ located on the supero-posterior part of the larynx, called the
palatal papillaries. A few filiform papillæ stud the roof. The pharynx
communicates anteriorly with the posterior nares and the mouth, and,
posteriorly, with the esophagus and the larynx.
Shape.—The pharynx is a musculo-membranous sac.
Structure.—The pharynx is lined with a mucous membrane covered by
squamous epithelium. The mucous membrane is thrown into irregular folds.
The bird has two Eustachian tubes. Pneumatic apertures conduct the air
from the Eustachian tubes to the pericranial diploë.
In the posterior pharyngeal roof is situated the infundibular crevice.
Function.—The function of the pharynx is to give passage for the air
from the posterior nares to the larynx, and to give passage for the food from
the mouth to the esophagus.
Glands Adjacent to the Mouth and to the Pharynx.—The mucous
membrane adjacent to the glottis and in the roof of the mouth contains
alveolar glands. The angular gland of the mouth, located beneath the
zygomatic arch, by some anatomists is considered the rudimentary parotid
gland. The sublingual glands, or glandulæ sublinguales, are well developed
(Fig. 17, No. B, 4). They form conical masses, with the apex directed
anteriorly, and occupy a portion of the intermaxillary space. Several ducts
from these glands open into the mouth cavity. In the palatine region there
are also located glands called the palatine glands, which open by many
stomata upon the surface.
The Esophagus (Fig. 18, No. 6). Location and Shape.—The esophagus
is a musculo-membranous tube, capable of great distension, which extends
from the pharynx to the proventriculus (Fig. 35, No. 1, and 3).

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The esophagus communicates anteriorly with the pharynx. It extends
down the neck, lying supero-laterally with regard to the trachea and toward
the right side. It enters the thorax above the trachea, and, passing through
between the bronchi, terminates into the proventriculus. At the entrance of
the thorax and just to the right of the median line, it expands into the crop
which divides it into two portions, designated as the first and the second.
The first portion of the esophagus is the longer, the length depending upon
the size and kind of fowl.
Structure.—The wall is composed of four coats, the mucous membrane,
the submucosa, the muscular coats, and the fibrous sheath or tunic. The
mucous membrane is pale and is covered with stratified squamous
epithelium.
The mucous membrane is loosely attached to the muscular coat by the
submucosa. Except during deglutition it lies in longitudinal folds which
obliterate the lumen. Opening from the mucosa are lenticular glands, which
may be seen on inflating an esophagus and looking through its transparent
walls.
The muscular coat of the esophagus is divided into two layers, an outer
longitudinal and an inner circular layer.
The outer fibrous sheath connects the esophagus loosely to the
surrounding structures.
Function.—The function of the esophagus is to give passage way for the
food from the pharynx to the crop and from the crop to the proventriculus.
The Crop (Fig. 35, No. 2; Figs. 30 and 31). Location and Shape.—The
crop, or ingluvies, saccular in shape, is located at the entrance of the thorax
and just to the right of the median line. The first portion of the esophagus
empties into the crop superiorly and inferiorly the crop opens into the
second portion of the esophagus. Like the esophagus the crop is capable of
great distension.
Structure.—The wall of the crop is composed of four coats, the mucous
membrane, submucosa, muscular and the outer fibrous.
The crop is lined with mucous membrane containing mucous glands
which secrete a mucus to keep the surface moist. The surface of the mucous
membrane is covered by stratified squamous epithelium.
The submucosa connects the mucous membrane to the muscular coat.

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The wall of the crop is provided with strong muscles. The fibrous coat, or
tunic, connects it with the surrounding structures.
Function.—The crop is a storehouse for the food during the hours of
feeding, the food when needed by the stomach being gradually discharged
from the crop by the contraction of its muscular walls. The subcutaneous
cervical muscles which cover this reservoir aid in this discharge.
In the act of deglutition, the food, after being subjected to the fluid
supplied in the mouth by the adjacent glands, is poised upon the tongue and
swallowed partly by a sudden jerk of the head, and partly by means of the
pressure of the tongue against the hard palate, the food then passes down
the esophagus and lodges first in the crop, till needed by the stomach, when
it is passed through the second portion of the esophagus to the first portion
of the stomach, the proventriculus. The time during which food remains in
the crop depends upon the nature of the food. Animal food will, in part, be
retained about eight hours and vegetable foods may not all be passed on for
from sixteen to eighteen hours.
The Stomach (Fig. 31, No. 7; Fig. 32, B).—The stomach, or ventriculus,
of fowls is made up of two portions, namely, the pars glandularis, or
proventriculus, and the pars muscularis, or gizzard.
The Proventriculus. Location.—The proventriculus lies in the superior
part of the groove formed by the two lobes of the liver, is inferior to the
aorta, and is directed slightly to the left, communicating anteriorly with the
second portion of the esophagus and posteriorly emptying into the pars
muscularis, the gizzard.
Shape.—The proventriculus is round transversely and elongated, in fact,
nearly fusiform. In the hen of average size it measures about 1.62 inches
long and 0.8 inch in diameter.
Structure.—The wall of the proventriculus has four coats, the mucous,
submucous, muscular, and serous.
The inner mucous coat which is raised in folds, is lined with columnar
epithelial cells. The mucous membrane contains lymphoid tissue. The
mucous coat throughout contains simple tubular glands which secrete a
highly acid fluid which finds its way to the surface through small
cylindrical ducts lying at right angles to the inner surface of the mucous
membrane (Fig. 32, No. B, 1).

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Fig. 32.—Gizzard and stomach of the
fowl.

A. 1, Alveolar glands. 2, Mucous
membrane of the inner surface of the
proventriculus showing the tubular
glands. 3, Connective tissue between the
alveolar glands. 4, An artery. 5,
Muscularis mucosa.

B. Photograph of the proventriculus and
gizzard. 1, Proventriculus showing
stomata of glands. 2, End of duodenum.
3, Gizzard showing hornified epithelium
formed into grooves. 4, The heavy
muscular walls.

The submucosa, connects the mucous and muscular coats and the
muscularis layer throws the mucous membrane into folds.
Outside the muscularis mucosa there is another layer (Fig. 32, A), of
simple tubular glands, grouped in lobules, and lined by cuboidal cells and

Page 161

separated from each other by clefts. These tubular glands converge toward
the center and open into the same cavity.
The middle muscular coat can be divided into three layers: two thin,
longitudinal layers, and a thick, circular layer interposed between the other
two.
Function.—The function of the proventriculus appears to be to soak the
food with a secretion. The secretion from the proventriculus is similar to
that produced by the fundus glands of the stomach of mammals. It contains
acid and a ferment-pepsin.
The Gizzard (Fig. 31, No. 18). Location.—The gizzard, or muscular
stomach, occupies a portion of the central part of the abdominal cavity (Fig.
33, No. 4). It lies slightly to the left and just behind the liver, the
proventriculus, and the spleen, and rests upon a mass of intestines. The
gizzard communicates at its anterior portion with the proventriculus and
with the duodenum. These openings are close together. The gizzards of a
large number of hens of average size averaged in weight as follows: full,
0.215 pound; empty, 0.126 pound. The gizzard stands perpendicularly and
somewhat obliquely in the abdominal cavity.
Shape.—In shape the gizzard is roundish, flattened laterally.
Structure.—The walls of the gizzard are very thick and are made up of
three coats: mucous, muscular, and serous.
The cavity of the gizzard is covered by a thick skin-like structure
possessing a heavy stratified squamous epithelial layer which is thrown
somewhat into ridges (Fig. 32, B). This membrane becomes thinnest near
the edges.
The mucous membrane, being cornified and readily detachable, is by
some anatomists considered as a special membrane (Fig. 37, B).
At the pyloric opening there is a valve formed by a fold of the mucous
membrane, which prevents grit and large particles of food from passing out
of the gizzard.

Page 162

Fig. 33.—View of viscera of the left side of a hen. 1, The base of the heart. 2,
Proventriculus. 3, Left lobe of the liver. 4, Gizzard. 5, End of the duodenal loop.
6, Pancreas. 7, Free portion of the small intestine. 8, Lungs. 9, Diaphragm.

Fig. 34.—View of the viscera of the right side of a hen. 1, Base of the heart. 2,
Lungs. 3, Right lobe of the liver. 4, Duodenal loop. 5, Pancreas. 6, Cæcum. 7,
Large intestine or rectum. 8, Free portion of the floating small intestine. 9, Gall-
bladder. 10, Right kidney. 11, The ribs. Note the lungs pushing up between them.

On each side it has a powerful fleshy muscle, the muscularis lateralis.
These musculares laterales are hemispherical, consist of very closely
packed fibers extending transversely, and are attached to strong anterior and
posterior ligamentous tendons. They are joined at the edge of the organ by a

Page 163

strong aponeurosis. The muscular fibers are red but do not possess cross
striations; they are of the smooth type. The muscularis intermedii, thinner
and less developed than the musculares laterales, occurs on each of the
anterior and the posterior parts of the gizzard.
The serous coat covers over the greater part of the external surface of the
gizzard and closely adheres to the muscular coat.
Function.—The hard callous pads of the gizzard, operated by the
powerful muscles above described, together with grit, act like mill stones
and make reduction to fineness very complete.
At the posterior part there is a sacculated portion containing glands of the
long tubular type which secrete a fluid ferment similar to that secreted by
the glands of the pyloric portion of the stomach of mammals. These glands
also exist in a small band near the entrance of the gizzard. Here the food is
mixed with strongly acid secretion containing pepsin which makes gastric
digestion perfect.

Fig. 35.—A median antero-posterior section through the body of a 1-pound
pullet. 1, First portion of the esophagus. 2, Crop. 3, Second portion of the
intestine. 4, Proventriculus. 5, Gizzard. 6, Spleen. 7, Liver. 8, Heart. 9, Point
where duodenum was severed from gizzard. 10, Point where duodenum was
severed. 11, Duodenum. 12, Pancreas. 13, Cæcum. 14, Floating small intestine.
15, Ovary. 16, Oil sac.

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The Small Intestine (Fig. 31, No. 8 and 9).—The small intestine,
intestinum tenue, is the tube which connects the gizzard with the large
intestine. It is divided into two parts, the duodenum and the free portion. Of
the three parts as considered in the mammalian intestine, only the first, the
duodenum, can be distinguished. There is no demarcation between the
jejunum and the ileum. The jejunum and the ileum or that part which
represents these sections, are in coils suspended from the free border of the
mesentery the other border of which is, in turn, attached to the dorsal wall
(Fig. 64). The length of the small intestine in a hen of average size is about
61.7 inches.

Fig. 36.

A. Section of the duodenum of the fowl.
1, Villus. 2, Gland. 3, Mass of lymphoid
tissue. 4, Muscularis mucosa. 5,
Longitudinal layer. 6, Circular muscular
layer. 7, Serous layer.

B. A section from A at a. 1, The striated
free border of the cells. 2, Goblet cell. 3,
Columnar cell. 4, Nucleus of cell.

The wall of the small intestine is provided with four coats, as follows: a
mucous, submucous, muscular coat made up of two layers—the outer,
longitudinal and the inner circular layer, and an external serous.

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Fig. 37.—Histological studies of various anatomical parts.

A. A transverse section of the first portion of the esophagus of a fowl. 1, The
outer longitudinal muscular layer. 2, The circular muscular layer. 3, The
submucosa. 4, The muscularis mucosa. 5, Stroma. 6, Epithelial layer. 7, The
lenticular glands. 8, The lumen.

B. A transverse section of the proventriculus. 1, The outer longitudinal muscular
layer. 2, The middle muscular layer. 3, The inner longitudinal muscular layer. 4,
Stroma. 5, The muscularis mucosa. 6, The submucosa. 7, Stroma. 8, Tubular
glands. 9, Tubulo-alveolar glands. 10, A tubulo-alveolar gland with the tubular
glands cut transversely, 11, The lumen of the proventriculus.

C. A section of the inner wall of the gizzard. 1, The hyaline mucous membrane.
2, Branched tubular glands. 3, Submucosa. 4, Muscle. 5, A connective tissue
septum.

D. A transverse section of the small intestines. 1, The outer longitudinal muscular
layer. 2, The inner circular muscular layer. 3, The muscularis mucosa. 4, The
stroma. 5, Brunner’s glands. 6, A villus. 7, Mass of lymphoid tissue.

E. A transverse section through the cecum. 1, The outer longitudinal muscular
layer. 2, The inner circular muscular layer. 3, The submucosa. 4, The muscularis
mucosa. 5, The stroma. 6, Tubular glands. 7, The lumen.

F. The cerebellum showing the arbo-vitæ. 1, White, fiber portion. 2, The granular
layer. 3, The layer of Purkinje cells. 4, The molecular layer.

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The mucous membrane which lines the intestine is thick, soft, and highly
vascular. It has a velvety appearance, due to numerous long, thin projecting
villi. The villi (Fig. 36, A) are concerned in the absorption of the digested
food, absorbing principally the emulsified fats. Each villus is covered with a
single layer of high columnar epithelial cells. Some of these, the so-called
goblet cells, provide mucin which lubricates the mucous surface. These
cells are found in all mucous surfaces and prevent the surface from
becoming dry. There are a few goblet cells near the summits of the villi.
Openings of simple intestinal tubular glands the duodenal glands, or the
glands formerly known as Brunner’s glands, are located between the villi.
These glands secrete the succus entericus, or intestinal juice. These
openings, or stomata, are lined with granular cells. The reaction of the
contents of the small intestine is strongly acid, but gradually less so in
proportion to the distance down the intestinal tract until the cæca are
reached, where the reaction is found to be faintly acid, neutral, or slightly
alkaline.
Function.—The function of the small intestine is that of digestion and
absorption.
The Duodenum. Location and Shape.—The duodenum, a small tube,
originates from the gizzard about ½ inch to the right of the entrance of the
proventriculus. Extending from left to right, it passes under and behind the
gizzard along the inner side of the right abdominal wall backward to the
posterior portion of the wall, and a trifle more than half way toward the left
side, where the loop rests. This loop, the duodenal loop, is about 5 inches in
length (Fig. 31, No. 8). The two branches of the loop the first and the
second portions or the descending and ascending limbs, are loosely held by
connective tissue, and have the pancreas lodged between them.
The Free Portion of the Small Intestine. Location.—That section of the
small intestine following the duodenum is called the free portion of the
small intestine and occupies the space between the abdominal air-sac and
the median line of the abdominal cavity. It is disposed in coils and is
suspended from the dorsal wall of the abdomen by a thin membrane, the
mesentery.
The bile ducts enter the small intestine about 14 inches from its point of
origin. The pancreas also pours its contents into the small intestine.

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The Large Intestine (Fig. 31, No. 12). Location.—The large intestine
extends in a straight line along the inferior border of the vertebral column
communicating anteriorly with the small intestine, and the cæca and
posteriorly with the cloaca.
Shape.—The diameter of the large intestine is approximately twice that
of the small intestine. In fowls of average size its mean length is 4.61
inches. The large intestine has sometimes been spoken of as the rectum, or
straight gut.
Structure.—Like the small intestine the large intestine has four coats: an
inner mucous, a submucous, a middle muscular and an outer serous. The
folds of mucous membrane of the large intestine have tubular glands lined
with columnar cells (Fig. 37, A, No. 1).
Function.—The large intestine is similar in function to that of the small
intestine, in that digestion and absorption may take place within it.
The Cæca (Fig. 31, No. 11). Location.—The fowl has two cæca
extending forward from their point of origin at the juncture of the small and
large intestine.
Shape.—The cæca average 7.61 inches in length. They are large in
caliber toward the blind extremity and are constricted near their origin.
Structure.—The parietal coats are continued from the small intestine.
Ebarth has described an elevated body in the cæcum, which is located
about 4 millimeters from the opening and is composed entirely of lymphoid
tissue.

Page 168

Fig. 37A.—Photomicrograph of a
transverse section of large intestine and
oviduct just anterior to the cloaca,
showing the tubular glands of the large
intestines, mucosa of oviduct with
intervening structures. 1, The tubular
glands of large intestine, or rectum. 2,
Muscular wall of intestine. 3, Wall of
the oviduct. 4, Mucosa of the oviduct.

The cæca are usually partly filled with a soft pultaceous material of a
pasty consistency.
The Cloaca (Fig. 31, No. 13). Location.—The rectum opens by a
circular, valvular orifice into the dilated portion just in front of the anus,
which dilatation is called the cloaca.
Shape.—The cloaca is saccular in shape.
Structure.—The cloaca is divided into two portions, the coprodeumal and
the urodeumal. That portion of the cloaca into which the intestine empties is
called the coprodeum; and the ureter and oviduct empty into the urodeum.
The seminiferous tubules, carrying the semen from the testes in the male
empty in teatlike projections on the cloacal mucous membrane into the
urodeumal portion. The cloacal walls are similar in structure to the large
intestines.
On the dorsal wall of the cloaca between it and the spine, is a small sac,
called the bursa of Fabricius, which has a duct communicating with the
cloaca. The mucous membrane of this sac is thrown into folds and is
studded with glands. The bursa of Fabricius is larger in the young than in
the adult bird. It apparently atrophies as the bird becomes older. When the

Page 169

bird is four months old this bursa is best developed, and at this age it may
be as large as 2 or 3 centimeters in diameter.
Function.—The function of the cloaca is to give passage way to the
feces, the urine, and the egg and to act as an organ of copulation.
Course of the Food.—The food first enters the mouth, after being picked
up by aid of the beak. From here it passes through the pharynx and first
portion of the esophagus to the crop, without mastication, as the bird is not
provided with teeth. The food is passed from the crop by aid of its muscular
walls as needed; thence through the second portion of the esophagus to the
proventriculus, an expansion in the digestive tube just before it terminates
in the gizzard. The glands of the proventriculus produce a secretion in
which the food is soaked before passing into the gizzard. The gizzard is
provided with strong muscular walls which, by aid of grit, thoroughly
reduce the food to fineness. From the gizzard the food passes through the
first portion of the small intestine, where it is subjected to the action of the
bile from the liver, the pancreatic juice from the pancreas, and of the succus
entericus from the glands of the intestinal wall. The food is then passed into
the cæca. The indigestible portion of the food passes from the cæca through
the large intestine, or rectum, to the cloaca and thence to the external world.
The digestive functions of the bird are very potent and rapid. This
compensates for the waste caused by their extensive, frequent, and energetic
motions, and is in accordance with the rapidity of their circulation and their
high state of irritability.

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THE ACCESSORY ORGANS OF DIGESTION

The accessory organs of digestion are the liver, pancreas, and some
anatomists include also the spleen. The first two manufacture fluids
containing ferments which aid in splitting or digesting the food.
The Liver (Figs. 31, 33 and 34). Location.—The liver, hepar, lies
ventrally and posteriorly to the heart. It is related anteriorly with the
diaphragm, inferiorly with the sternum, posteriorly with the gizzard and
intestine, and superiorly with the ovary, oviduct and proventriculus and
laterally with the abdominal wall.
Shape.—The liver is a voluminous deep livid brown gland, soft and
friable in texture. It is divided into two principal lobes, a right and a left.
The right lobe is larger than the left. In the hen of average size the liver
weighs 35 grams. The parietal surface is convex and smooth. The surface
which lies against the viscera is irregularly concave. The visceral surface
furnishes exit for the bile duct and passage for the nerves and blood-vessels.
This part is called the porta.
The left lobe may be cleft from below so deeply as to form two lobes on
that side.
Structure.—Each lobe is covered by a double serous membrane, one
closely adherent, the other surrounding the structure loosely. These tunics,
which are reflections of the peritoneum, are continued from the base of the
liver, over both the anterior, and the posterior surface. The loose layer is
formed by the air cells surrounding the lobes. The thin border of the liver is
usually free.
The two lobes of the liver are connected by a narrow isthmus of liver
tissue. Occasionally there is a bird in which there occurs a lobus Spigelii
located at the posterior of the liver between the two principal lobes.
The apex of the heart sacculates the diaphragm backward, so that part of
this apex lies between the right and the left lobes (Fig. 43, No. 6 and 7). A
ligament, the falciform, extends from the apex of the pericardial membrane,
and attaching it rather firmly to the central connective tissue, or interlobar
ligament. This ligament also has attachments to the inner surface of the

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sternum. The broad ligament of the liver is formed posteriorly by a fold of
the peritoneum.
The interlobar, or principal, ligament of the liver is formed by a large
and strong duplicature of the peritoneum, which makes a longitudinal
division in the abdominal cavity similar to the lateral division made by the
thoracic mediastinum in mammals. It is reflected upon the pericardium
from the linea alba and the middle line of the sternum, and passes deeply
into the interspace of the lobes of the liver. It is attached to these lobes
throughout their whole length and connects them below to one side of the
gizzard. The lateral and posterior part of the liver attach to the adjacent air
cells, and the whole viscus is thus kept fixed in its position during rapid and
violent movements of the bird.
The remains of the umbilical veins are traceable within the duplicature of
the membranes forming the septum. These remains thus represent the round
ligament of mammals.

Fig. 38.—Cellular structure of liver, pancreas, and trachea.

A. Liver. 1, Liver cells. 2, Sinusoid. 4, Nucleus of cells.

B. Pancreas. 1, Island of Langerhans. 2, Alveolar cells. 3, Duct.

C. Trachea. 1, Ciliated epithelia. 2, Glands. 3, Hyaline cartilage.

D. Section of wall of ovum at Fig. 57 letter d. 1, Yolk. 2, Granular membrane. 3,
Theca. 4, Blood-vessel.

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A microscopic study of the liver of the fowl shows a compact mass of
liver cells polyhedral in shape, with large nuclei (Fig. 38, A). The liver
tissue differs from that of mammals in that there is no clearly outlined
lobular arrangement; neither is the outline of the individual cell so well
marked. The parenchymatous portion is made up of columns of liver tissue.
These columns anastomose and show narrow channels between. They are
best seen in the young chick.
Function.—One of the functions of the liver is to secrete bile. A gall-
bladder, which receives part of the bile secreted by the right lobe of the
liver, is located on the posterior face of this lobe. Extending from this gall-
bladder there is a duct, the cystic duct, which empties into the small
intestine toward the extremity of the second branch of the duodenal loop.
Another duct called the hepatic duct, proceeds directly from the two lobes
of the liver and empties into the intestine just in front of the cystic duct.
The Pancreas (Fig. 31, No. 17). Location and Shape.—The pancreas, an
organ lying in the duodenal loop is a yellowish-white, lobulated gland,
elongated in shape. Its average length in fowls of average size is 4.96
inches, and the average weight about 0.008 pound. The pancreas is divided
into lobes, which in turn are divided into lobules.
Structure.—The pancreas has a supporting connective tissue. The lobules
are made up of small alveolar glands, which are lined with columnar
epithelial cells. The ducts leading from the alveoli are small; these unite to
form larger ducts in which the epithelium is taller. Between the alveoli
throughout the pancreas there are clusters of polyhedral cells which form
the islands of Langerhans. These islands are said to produce an internal
secretion, or hormone, which is absorbed by the blood or lymph capillaries
and thus enters the circulation (Fig. 38, B).
Function.—The function of the pancreas is to secrete a fluid containing
digestive ferments.
The Spleen (Fig. 31, No. 21). Location.—The spleen, or lien, lies in a
triangle formed by the proventriculus, the liver, and the gizzard.
Shape.—It is a reddish-brown body shaped like a buckeye, is small in
size, weighing only about 0.005 pound.
Structure.—The outer surface of the spleen is covered by a reflection of
the peritoneum. After this covering is removed, there is observed a firm,
white, fibrous layer, the cortical portion. This covering sends into the

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interior small and large trabeculæ, forming a framework and dividing it into
acini, or compartments. The spaces are filled with a dark red
parenchymatous material called splenic pulp. The framework, in both deep
and surface portions, are found elastic fibers and smooth muscular fibers.
The spleen is essentially a lymphatic organ, its peculiar structure
depending largely upon the arrangement of the blood-vessels. Compact
lymphatic tissue occurs in the spleen in spherical, oval, or cylindrical
collections of closely packed lymphoid cells. These masses are known as
the Malpighian bodies, or splenic corpuscles. They are distributed
throughout the splenic pulp. Each splenic corpuscle contains one or more
small arteries. These extend near the periphery of the corpuscle and more
rarely in the center.
The splenic artery passes in and the splenic veins out at the hilum which
is located on the concave, or attached, side of the spleen. The splenic artery,
upon entering the organ, at once branches, the trabeculæ forming a support
for the vessels.
After the arteries have entered the hilum, as stated above, they divide into
many branches which follow the septa of the connective tissue. At first the
arteries are accompanied by branches of the splenic veins. Soon, however,
the arteries leave the veins and the septa, and penetrate the splenic pulp. In
the splenic pulp the adventitia of the smaller arteries assume the character
of reticular tissue, and become infiltrated with lymphoid cells. This
infiltration forms masses which are called the splenic corpuscles, or
Malpighian bodies. The terminal arteries break up into capillaries, which
still retain an adventitia, and empty into border spaces, or sinuses,
sometimes spoken of as ampullæ. These sinuses in turn empty into
cavernous sinuses of the splenic pulp. From these are finally formed the
venules; and the collections of venules form the splenic veins through
which the blood gains exit from the spleen.
The Abdominal and Pelvic Cavities.—In birds the abdominal cavity is
divided into two smaller cavities by a fibrous septum. The anterior cavity
representing the abdominal contains the liver, and the other representing the
pelvic contains the gizzard, intestines and oviduct.
The Peritoneum and the Mesentery.—The abdominal and pelvic
cavities are lined by the peritoneum. Like all serous membranes this is
composed of a parietal and a visceral portion, which together form a

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complete sac, with the organs it covers situated on the outer side. The
peritoneum like other serous membranes consists of a mesothelial and a
submesothelial portion, the cells of the former being arranged in a single
layer. Since a serous membrane is so arranged as to line a closed cavity, and
at the same time to cover its contents, it follows that the entire membrane
must be a closed sac, the mesothelial layer being on the inside; such a sac is
called a serous sac, or cavity. Synovial membranes are also regarded as a
variety of serous membranes. The fold, or layer, of the membrane which
lines the cavity is called the parietal, that which covers the greater part of
the organs contained therein is called the visceral portion; the two surfaces
contacting, and gliding upon each other, are lubricated by a fluid secretion
contained in the sac; hence one use of these membranes is to prevent
friction between the walls of cavities and the organs contained therein.
Serous membranes line the abdominal cavity, pericardium, cavities of the
heart and is continuous throughout the vascular structures.

Fig. 39.—A transverse section of body
of hen through 15, Fig. 34. R, Right
side. L, Left side. 1, Spinal cord. 2,
Esophagus. 3, Trachea. 4, Skin. 5,
Pectoral muscles.

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The serous membrane besides covering the external surface of the
viscera, double folds pass from one organ to another, or from an organ to
the parietes of the cavity. These double folds of the peritoneum are known
as ligaments, or as mesenteries. In ligaments the two folds are strengthened
by an interposed layer of fibro-elastic tissue. A mesentery is a broad, double
fold of peritoneum, attached to the abdominal parietes above, and
containing a portion of the intestine in its free or remote extremity. Between
its folds we find blood-vessels, nerves, and lymphatics or lacteals, hence it
permits vascular and nervous communications with the organ attached to it.
The free portion of the small intestine is attached to the free margin of the
mesentery.

Page 176

THE RELATIONS OF THE VISCERAL ORGANS OF THE
DOMESTIC FOWL

Fig. 40.—Transverse section through
the body of a hen through 14, Fig. 34. R,
Right side. L, Left side. 1, Spinal cord.
2, Esophagus. 3, Trachea near inferior
larynx. 4, Lungs. 5, Pectoral muscles.

Figure 33 shows a fowl with the left abdominal wall and the left thoracic
wall removed. No. 1 in this figure shows the base of the heart in front of the
left lobe of the liver. Above the liver is the proventriculus; above this, the
diaphragm; and above the diaphragm and the base of the heart the left lung
occupying the superior part of the thoracic cavity, and that there is no
distinct pleural sac, as in mammals but that the lung pushes out between the
ribs, thus pressing against the ribs on the inner and the lateral sides. The
gizzard is back of the liver, to the left side of the abdominal cavity, and
beneath and in front of the duodenal loop. The small intestine from this side

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is above the gizzard. Supero-anterior to the gizzard is the blind end of the
cæcum. The pancreas is within the duodenal loop.

Fig. 41.—Transverse section through
the body of a hen at 12, Fig. 33. R,
Right side. L, Left side. 1, Spinal cord.
2, Esophagus. 3, Inferior larynx. 4, Base
of the heart. 5, Aorta. 6, Vena cava. 7,
Lungs. 8, Skin. 9, Pectoral muscles.

Figure 34 shows the viscera from the right side after the removal of the
right abdominal and the right thoracic wall. The base of the heart is in front
of the right lobe of the liver. Above these the right lung occupies the upper
part of the thoracic cavity as in the preceding illustration. Just back of this is
the anterior lobe of the kidney. The gall-bladder is observed at No. 9 on the
right lobe of the liver. Just inferior to a longitudinal central line is the
duodenal loop, between the limbs of which is seen the pancreas. Above this
loop the cæca are located. The gizzard is not visible from the right side; on
this side posterior to the liver is the small intestine. Superior to this at No. 7
the rectum.

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The relative position of the visceral organs in the median line is observed
in Fig. 35. No. 1 of this figure shows the stump of the first portion of the
esophagus, and No. 2, the left wall of the crop. Following this, and located
just below the vertebræ is the second portion of the esophagus. The major
portion of the crop is located on the right side.

Fig. 42.—Transverse section through
the body of a hen at 11, Fig. 33. R,
Right side. L, Left side. 1, Spinal cord.
2, Vertebra. 3, Spinous process of
vertebra. 4, Lungs. 5, Esophagus. 6,
Pericardial sac. 7, Sectioned surface of
heart. 8, Auricle of heart. 9, Blood clot
in right auricle. 10, Section of sternum.
11, Pectoral muscles.

It will be noted that the second portion of the esophagus passes over the
base of the heart and the superior part of the liver, and then terminates in the
proventriculus. The proventriculus extends downward and empties into the
gizzard. This organ lies antero-laterally to the gizzard, supero-posterior to
the liver, and to the left of the spleen. The spleen lies in a triangle formed
by the liver, the proventriculus, and the gizzard. The heart is noted to lie

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supero-anterior to the liver, and between the anterior portion of the fissure
formed by the right and the left lobe. The ovary is located back of the
diaphragm at the anterior end of the kidney and below the inferior surface
of the bodies of the vertebræ. The bulk of the floating portion of the small
intestine is located above the gizzard.

Fig. 43.—Transverse section through
the body of a hen at 13, Fig. 34. R,
Right side. L, Left side. 1, Spinal cord.
2, Body of vertebra. 3, Superior spinous
process of vertebra. 4, Lungs. 5,
Esophagus. 6, Heart. 7, Right and left
lobes of liver. 8, Sternum. 9, Skin. 10,
Pectoral muscles.

A transverse anterior section of a normal laying hen is shown in Fig. 39,
the section being made at 15 of Fig. 34. At this point the esophagus lies
centrally and above the trachea. Figure 40 shows a transverse anterior
section through the thoracic region at 14 of Fig. 34. At this point the
esophagus is slightly to the right of and is superior to the trachea. At this
level the apex of the lung is sectioned. This is in the region of the cervical
air-sac. Figure 41 shows a posterior section at 12 of Fig. 33. The esophagus

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here is above and to the right of the inferior larynx, and directly below and
between the lungs. The inferior larynx is above the base of the heart.
Figure 42 shows a transverse anterior section made at 11 of Fig. 33. It
shows that at this level the esophagus is centrally located and passes over
the base of the heart. The heart occupies the lower portion of the thorax and
the lungs the upper. Figure 43 shows a photograph of a transverse anterior
section of the body made at 13 of Fig. 34. At this level the apex of the heart
lies within the anterior fissure of the liver. The sectioned portion of the heart
shows the lower portion of the ventricle.

Fig. 44.—Transverse section through
the body of a hen at 12, Fig. 34. R,
Right side. L, Left side. 1, Spinal cord.
2, Articular surface of vertebral
segment. 3, End of rib. 4, Lungs. 5,
Proventriculus. 6, Liver showing
Glisson’s capsule. 7, Sternum. 8,
Pectoral muscles. 9, Skin.

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Fig. 45.—Transverse section through
the body of a hen at 10, Fig. 33. R,
Right side. L, Left side. 1, Spinal cord.
2, Body of vertebra. 3, Lungs. 4, Ova. 5,
Proventriculus. 6, Liver. 7, Sternum. 8,
Skin. 9, Pectoral muscles.

In this figure the lungs show, on the sectioned surface, the ends of some
of the larger bronchi. The esophagus is located above the heart. Showing
the relations of the visceral organs back of the heart girdle, photograph
number 44, gives an anterior section made at 12, Fig. 33. The lungs are
spread out occupying the posterior thoracic region and below at No. 10 is
the diaphragm. The diaphragm does not appear to have that rigidity and
firmness of position as in mammals. It is rather rudimentary. Below the left
lung and above the left lobe of the liver is the proventriculus. Note that the
viscus is empty and that the mucous membrane is thrown into folds. At this
point the liver occupies much of the abdominal cavity. Figure 45 is a view
of an anterior section made at 10, Fig. 33. In this section the lungs are
decreasing in caliber. The liver occupies much of the space in the lower
right abdominal quadrant, and above and to the right is the ovary with many
of the ova developing yolks. Below No. 4 which is a developing yolk, is the
proventriculus. Figure 46 is a view of an anterior section made at 9, Fig. 33.
At this level are shown sectioned surfaces of the kidneys, which lie on
either side of the spinal column. Below the spinal column and occupying

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the left upper quadrant is the ovary containing ova in the process of
developing yolks. To the right is the sectioned surface of one of the cæca
and below this and on the right side is the sectioned ends of many of the
loops of the floating portion of the small intestine. Occupying the left lower
quadrant is the sectioned surface of the gizzard and on the abdominal floor
and to the right of the gizzard, the posterior end of the right lobe of the
liver.

Fig. 46.—A transverse section through
the body of a hen at 9, Fig. 33. R, Right
side. L, Left side. 1, Spinal cord. 2,
Vertebra. 3, Kidneys. 4, Ovary. 5,
Cæcum. 6, Small intestine. 7, Gizzard.
8, Right lobe of liver. 9, Skin. 10,
Pectoral muscles.

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THE RELATIONS OF THE VISCERAL ORGANS OF THE
BABY CHICK
There is approximately 47 per cent. of the yolk retained in the abdominal
yolk sac of the baby chick at hatching. Figure 47 shows a photograph of a
longitudinal section through a baby chick. This figure shows all the
posterior portion of the abdominal cavity occupied with abdominal yolk.
The abdominal viscera are pushed forward, and as the yolk is gradually
absorbed the visceral organs gradually occupy their normal position.

Fig. 47.—An antero-posterior section through the body of a baby chick just
hatched. 1, Abdominal yolk sac. 2, Gizzard. 3, Liver. 4, Heart. 5, Intestines. 6,
Spinal cord. 7, Cerebrum. 8, Cerebellum. 9, Fat in the post-occipital region. 10,
The thymus gland.

Page 184

Fig. 48.—Transverse sections of the
body of a baby chick at hatching. R,
Right side. L, Left side.

A. A transverse section at A, Fig. 50. 1,
Spinal cord. 2, Esophagus. 3, Entrance
to thorax. 4, Stubs of the wings.

B. A transverse section at B, Fig. 50. 1,
Spinal cord. 2, Esophagus. 3, Lungs. 4,
Heart.

C. A transverse section through the body
at C, Fig. 50. 1, Spinal cord. 2, Lungs.
3, Esophagus. 4, Liver. 5, Heart.

D. A transverse section at D, Fig. 50. 1,
Spinal cord. 2, Proventriculus. 3, Liver.
4, Gizzard. 5, Intestine. 6, Kidneys. 7,
Gall-bladder.

Page 185

Fig. 49.—Transverse section through
the body of a baby chick.

E at E, Fig. 50. 1, Spinal cord. 2,
Kidneys. 3, Gizzard. 4, Intestines. 5,
Unabsorbed yolk. 6, Stubs of legs.

F. A section at F, Fig. 50. 1, Spinal cord.
2, Kidneys. 3, Intestine. 4, Unabsorbed
yolk.

G. A section at G, Fig. 50. 1, Anus. 2,
Umbilicus.

A section through this body Fig. 47 at A is shown in Fig. 48, A. At this
point the esophagus appears below the vertebral column. Figure 48, B, a
section through the body at Fig. 47, B, shows the apex of the lungs. In a
median line and below the lungs is the esophagus. Note the mucous
membrane thrown into folds. Here the heart is sectioned, showing both
auricles and both ventricles. This is a view looking forward. Figure 48, C, is

Page 186

a view of a posterior section made at Fig. 47, C. It shows the same relations
of the esophagus and lungs, but shows at this level both the right and the
left lobe of the liver. Between these lobes we note the sectioned apex of the
heart. Figure 48, D shows a posterior section at Fig. 47, D. At this level the
kidneys are above and infero-laterally to the spinal column. The intestines
are below the kidneys; and on the left side, between the kidneys and left
lobe of the liver, and near the abdominal wall, is the proventriculus.
Occupying the major portion of the inferior abdominal cavity are the right
and the left lobe of the liver, and between these the anterior border of the
gizzard. Note the gizzard sitting at an angle inclining toward the left side.
Figure 49, E shows a section at Fig. 47, E. Here the gizzard occupies the
left lower abdominal quadrant. To the right are the intestines; and directly
above the gizzard is a small portion of the anterior end of the abdominal
yolk sac. Infero-laterally are the kidneys. Figure 49, F, shows the kidneys
similarly located as in the preceding; and just below is the rectum
suspended by the mesentery. The rest of the cavity is occupied by the
abdominal yolk.

Page 187

THE URO-GENITAL SYSTEM

The uro-genital apparatus, or apparatus uro-genitalis, consists of two
groups of organs: the urinary and the genital. The former elaborate and
remove the chief excretory fluid, the urine; and the latter serve for the
formation, development, and expulsion of the products of the reproductive
glands.

Page 188

THE URINARY APPARATUS (Fig. 50 and Fig. 51).

The urinary apparatus of the bird consists of two kidneys, from each of
which a ureter extends and empties into the cloaca.
The Kidneys. Location.—The kidneys are located in excavations in the
pelvic roof. They are related internally with the posterior aorta and vena
cava, supero-internally with the lumbo-sacral vertebræ and superiorly and
supero-externally with the ilium. The abdominal visceral organs lie below
the kidneys. The kidneys are external to or above the peritoneum.
Shape.—In the fowl of average size the kidneys are 2½ inches long and
are made up of three irregular lobes. The anterior lobe is usually the largest
and the middle the smallest. The anterior border of the first lobe is located
opposite the last true dorsal articulation. The anterior lobe is called the
anterior pelvic or ilio-lumbar lobe, the middle the middle pelvic or ilio-
sacral lobe, and the posterior the posterior pelvic lobe.
Structure.—The whole kidney has a fine transparent covering. The dark,
brownish-red parenchyme can be seen through this membrane. It has a
blood vascular system and a urinary tubular system. The larger arteries, the
veins, and the nerves pass between the lobules, and the smaller vessels
between the tubules. These form fine network or plexuses. The lymphatic
vessels are very few, and are mainly found on the surface. The kidneys are
pierced in their posterior third by the external iliac artery and at about its
middle by the venous branches forming the posterior vena cava.
The lobes are made up of lobules, which are plainly perceptible from the
external surface. Each lobule is apparently a unit within itself. It receives its
blood supply from small branches of the renal artery and is made up of a
cortical or peripheral portion which contains the glomerules (Fig. 52, A) and
a medullary portion, which is made up of tubules, or urinary canals,
arteries, veins, and nerves.

Page 189

Fig. 50.—Photograph showing spinal cord and relative positions of the kidney,
lung and heart. 1, Heart. 2, Lung. Note the indentations made by the ribs. 3, The
anterior, middle and posterior lobes of the kidney. The lobules are plainly visible.
4, The lumbo-sacral segment of the spinal cord. 5, Terminal cord filament. 6, The
cervico-dorsal segment of the spinal cord. 7, The brachial nerve plexus. 8 and 9,
The lumbo-sacral plexus. 8, The ischiadic nerve. 9, The lumbar nerves.

The urinary canals are divided into two kinds, namely, the outer and the
inner tubular systems. The outer canals, called the tubulæ uriniferi
corticalis, are very small in caliber and are located in the lobules. The renal
artery (Fig. 53, No. B, 3) breaking up into arterioles in the kidney, and
finally reaching the cortical portion of the lobules, form capillary plexuses
in the shape of minute spheres, which are the glomerules (Fig. 53, No. C, 3
and B, 5). Around each glomerule there is formed a capsule called
Bowman’s capsule, which is the beginning of the uriniferous tubule. This
entire mass is called the Malpighian body, or renal corpuscle. This capsule
then extends as the urinary, or secreting tubule, being at first constricted,
then convoluted, and terminates into a second portion, the descending limb
of Henle. This portion of the tubule becomes constricted. It then forms the
loop of Henle and ascends as the second portion, or second limb of Henle,
which is again of greater diameter. The top of the secreting tubule is slightly
wavy and empties into the collecting tubule along with many others. These
collecting tubules in turn merge into large tubules which finally empty into
the ureter (Fig. 53, No. 14). These collective bundles correspond to the
pyramids of the kidneys of mammals.

Page 190

Fig. 51.—The kidneys. 1a, The posterior. 1b, the middle and 1c, the anterior
lobes of the kidney. 2, The posterior aorta. 3, The external iliac or crural artery.
4, The ischiadic artery. 5, The sacralis media artery. 6, The ureter which empties
into the cloaca at 7. 8, The external iliac vein. 9, The internal iliac vein. 10, The
iliacus communis.

Page 191

Fig. 52.

A. Photomicrograph of a section of a
kidney showing three lobules. 1,
Cortical portion of lobule showing
glomeruli. 2, The central or medullary
portion of the lobule. 3, The outer
surface of the kidney.

B. Salts from the urine of a hen. 1, Uric
acid crystals. 2. Sodium urate crystals.

Page 192

Fig. 53.—The renal structure.

A. 1, Capillary blood-vessel. 2,
Descending limb of Henle. 3, Collecting
tubule. 4, Ascending limb of Henle.

B. 1, Branch of renal artery. 2, The
descending or medullary branch. 3, The
ascending branch. 4, The arteriole
taking part in the formation of the
glomerule. 5, The glomerule. 6,
Bowman’s capsule. 7, Blood-vessel
extending from the glomerule. 8, The
vein of the medullary part of the lobule.
9, The neck. 10, The convoluted tubule.
11, The descending limb of Henle. 12,
Henle’s loop. 13, The ascending loop of
Henle. 14, The collecting tubule.

C. 1, Section through a convoluted
tubule. 2, Bowman’s capsule. 3, The
glomerule.

The neck of the uriniferous tubule as it emerges from Bowman’s capsule
is short and narrow and is lined with a few cuboidal cells. Toward the

Page 193

glomerular end the cells are of a transitional form gradually merging into
the flat squamous type peculiar to Bowman’s capsule. The first convoluted
tubule is lined with irregular cuboidal or pyramidal epithelial cells. The
descending limb of Henle’s loop is narrow and is lined with a simple layer
of flat epithelial cells. In the loop the epithelium changes from the flat type
in the descending limb to the cuboidal in the ascending limb. The ascending
limb of Henle’s loop again becomes broader and is lined with low cuboidal
cells. The second convoluted, or tortuous, tubule is lined with low cuboidal
cells as are also the collecting tubules. The collecting tubules originate from
every part of the internal substance of the lobules, and extending to the
gyrations, uniting in the pinniform structure and traversing to the margin of
the lobules, following along the uneven surface, infero-laterally and toward
the median body line, finally empty into the ureter.
There are many arterial branches given off from the arteria renalis. The
arteries which supply the kidneys are given off from the posterior aorta and
ischiadic artery. As soon as these arteries enter the kidney they break up
into two systems. One system supplies the kidney substance with
nourishment in the form of nutrient blood; the second system supplies the
glomerules with what may be considered functional blood (Gadow). The
second system of arteries branches into the small arteria interlobularis,
which pass between the lobules of the kidneys where they give off side
branches which penetrate the cortical portion of the lobules and form the
capillary plexus, the glomerule.
The arteriole that enters into the structure of the glomerule is lined with
endothelial cells and is surrounded by a few muscle fibers and a fine
network of connective tissue. The vessel that carries the blood away is
similarly constructed.
Function.—In the glomerules the liquid portion of the urine is filtered out
of the blood, which urine flows through the uriniferous tubules and passes
from the kidney through the ureter. In the cubical cells are extracted the
solid portions of the urine which also pass through the tubules with the
liquid. The urinary secretion, as found in the ureter, does not contain much
liquid, but, on the contrary, is made up of a pasty material consisting of salts
which are, for the most part, uric acid crystals and sodium urate (Fig. 52,
B). This material becomes hard, like cement, soon after being exposed to

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the atmosphere. This secretion may be noted as a whitish pasty material on
the outer parts of the feces, or droppings, voided by the birds.
The Ureter. Location.—The ureter extends along the inferior surface of
the kidney. It has its origin near the anterior extremity of the kidney, and
passing posteriorly the entire length of the kidney receives tributary
collecting tubules, and terminates in the upper wall of the cloaca in the
urodeumal portion.
Shape.—The ureter gradually enlarges in diameter until it reaches the
posterior border of the kidney, and then maintains about the same caliber
throughout the rest of its course.
Structure.—The ureter wall is made up of three coats as follows: mucous,
muscular and fibrous.
Function.—The ureters serve as a passage way for the urine from the
kidneys to the cloaca.

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THE MALE GENERATIVE ORGANS (Fig. 54)

The male generative organs in the fowl consist of two testicles and an
excretory apparatus, the vas deferens, for each.
The Testicles. Location.—The testicles are located in the sublumbar
region of the abdominal cavity, behind the lungs, below the anterior
extremity of the kidneys, and opposite the last three ribs.

Fig. 54.—The pelvic organs of a cockerel. A, Testes. B, Rectum. C, Cloaca. D,
Vas deferens. E, Kidney. F, Adrenal gland. G, Lungs. H, Ureter.

Shape.—The testicles are ellipsoid in shape; their size varies with the
different species of birds. The two in the same bird are usually of the same
size, though one testicle may be slightly larger than the other. In a summary
of a large number of weights of the testicles of ten months old cockerels,
the average weight was 0.021 pound each. The average measurements were
2 inches in the major diameter and 1 inch in the minor diameter. In the
cockerel before sexual maturity, which is denoted by the male bird’s
crowing, the testicles are very small. They resemble, in shape, a navy bean
and are yellowish-white in color.
Structure.—The testicle is surrounded by a thin fibrous capsule, which,
in the mature cock, is very vascular. This capsule sends into the interior of

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the gland, septa which form the framework, or supporting structure. This
framework forms the spaces in which are located the glandular substance.
The glandular portion consists of the tubuli seminiferi, which are lined with
cubical cells. The framework supporting these tubules gives passage to
arterial branches of the spermatic artery, which furnish an abundant blood
supply; the framework also supports the veins returning the blood from the
testicle. The seminiferous tubules end in blind extremities in the
epididymus or globus minor, and unite in the seminiferous canals. All
arteries, veins, lymphatics, and seminiferous tubules enter or leave through
the globus minor at the attached portion of the testicle. The epididymis is
made up largely of convoluted tubules which are the continuation of the
secreting tubules of the globus major. The walls of the tubules of the globus
minor become thicker and are provided with smooth muscle cells in
addition to the connective tissue and endothelial lining. The convoluted
tubules empty into the vas deferens. The epididymus is covered by the
fibrous capsule; which corresponds to the tunica albuginea of mammals and
may be considered as a reflection or modification of the visceral
peritoneum.
The substance of the testicle is very soft; in fact, it may be said to be of
the consistency of encephaloid material. It is made up of secreting tubules
in which are found the spermatozoa; it also contains cells which produce an
internal secretion, or hormone. There is also produced some fluid in which
the spermatozoa float, the whole material manufactured constituting the
semen.
The spermatozoa of the fowl are provided with long cylindrical bodies,
which may be straight or wavy (Fig. 55, A). The body of the spermatozoon
is obtuse anteriorly, and posteriorly, tapers into a filimentary tail, or
flagellum, of varying length, by the aid of which the spermatozoon moves
about in the fluid.
The histological structure of the testicles of the baby chick at hatching is
approximately one-half white fibrous connective tissue. The seminal
tubules are small and widely distributed among the connective tissue. The
cells of these tubules possess rather large nuclei, round in shape, with linin
network and chromatin granules, typical of resting germ cells. As the bird
develops the testicles grow, the seminal tubules become larger, and the
amount of connective tissue correspondingly less.

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Fig. 55.

A. Spermatozoa of a cock. a, The
spermatozoa. b, The head. c, The tail.

B. The oviduct of a hen removed. A, The
oviduct. B, The superior ligament. C,
The inferior ligament. Note the oviduct
thrown in folds and the anastomosing
blood-vessels.

In addition to the tubules, the spermatogenic cells, and the connective
tissue, there is also in the testicles more or less fat. There is a small amount
of connective tissue between the seminiferous tubules, in which locations
there are also clusters of polyhedral cells, with round nuclei, others are the
interstitial cells.
The Vas Deferens (Fig. 54, D). Location and Shape.—Extending from
the epididymus, is the vas deferens which runs backward on the infero-
internal surface of the kidney and to the outside of the ureter. It is very

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tortuous passing on the infero-lateral surface of the kidney in company with
the ureter and becoming somewhat expanded posteriorly it terminates in the
upper wall of the cloaca in a rather small papilla located in the uro-genital
portion of the cloaca anterior to the mouth of the ureter. This papilla is the
organ of copulation and in ducks is very large, and spirally elongated, and
retractile forming a kind of penis. The papilla is traversed by a furrow on
the upper surface through which the semen flows.
Structure.—The vas deferens is covered and supported by the
peritoneum. Its wall is made up of a fibrous structure in which may be
found smooth muscle fibers. The wall does not possess glands. It is lined
with columnar epithelium. The posterior end is expanded and terminates
into a papilla. The base of the papilla is surrounded by a plexus of arteries
and veins, which serve as an erectile organ during the venereal orgasm,
when the fossa of the turgid papilla is everted, and the semen brought into
contact with the similarly everted orifice of the oviduct of the female, along
which the spermatozoa pass by undulatory movements of their ciliary
appendage, or tail.

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THE FEMALE GENERATIVE ORGANS (Fig. 56)

The female generative organs consist of one ovary and an oviduct.
Location.—The ovary is located similarly to the testicles of the male
bird, in the sublumbar region of the abdominal cavity, just at the anterior
end of the kidneys, posterior to the lungs, and slightly to the left of the
center.
Shape.—In the pullet the ovarian mass appears somewhat like a bunch of
grapes, being made up of from 3500 to 4500 small, whitish spheres, which
represent the undeveloped ova, and which in the active state are developed,
one by one, into yolks with their blastoderms. From the blastoderm the
fetus may later be developed. In the active ovary of the laying hen the
ovarian mass is of considerable size, as it contains ova in different stages of
development. Only one ovum is completely developed at a time, though
occasionally there may be only a few hours between the maturity of
successive ova. The ova receives nourishment from the blood-vessels of the
capsule, which vessels are branches of the ovarian artery.

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Fig. 56.—Functionating female generative organs of a hen. 1, Ova in process of
formation of yolk. 2, Stigmal line at which point the capsule ruptures when
ovum is mature. 3, The funnel end of the oviduct. 4, The oviduct torn loose and
laid to one side, the albumin-secreting portion. 5, The shell membrane secreting
portion. 6, The albumin. 7, The yolk. 8, The shell-secreting portion. 9, The
cloaca. 10, The rectum.

Structure.—The ovary contains very vascular cellulofibrous tissue. The
ovum as it develops is attached to the ovarian body by means of a delicate
white fibrous pedicle. When the yolk is mature it escapes from the
enveloping fibrous capsule by a cleavage of the capsule. The cleavage line
is called the stigmen (Fig. 56, No. 2). The yolk is surrounded by a very
delicate membrane called the vitelline membrane. The empty sac now
shrinks and finally disappears.
The Egg.—The principal divisions of the egg are the yolk, the albumin
outside of the yolk content, the shell membranes and the shell (Fig. 58). As
stated, the yolk is formed in the ovary, leaving the other three portions to be
formed in the oviduct.

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Fig. 57.—Section through the ovary of
the hen. a, The ova. d, An ovum
beginning to receive deposits of yolk
material. c, Ova farther advanced in
yolk formation.

The albumin may be subdivided into, first, a thin layer of albumin lying
close around the yolk; second, a thick layer of albumin lying at the outer
periphery; and third, a modification of the albumin called the chalazæ. The
chalazæ are twisted, dense cord-like structures at either pole of the yolk,
one end of which is adherent to the vitelline membrane and the other to the
inner membrane surrounding the albumin. The chalazæ thus act as stays to
this structure, which is carrying a delicate burden, the blastoderm.
The shell membrane consists of two layers, an inner delicate, and an
outer thicker layer. When the egg is just laid these two membranes are in all
parts closely adherent to each other, and the egg content completely fills the
shell cavity. As soon as the content cools there is a slight contraction; the
two shell membranes separate at the large end of the egg, forming an air
cell which gradually enlarges as the evaporation of liquid through the pores
of the shell takes place.

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Fig. 58.—A diagram of the parts of the egg. a, The blastoderm. b, The shell. c,
The outer shell membrane. d, The inner shell membrane. e, The air-sac at the
large end of the egg. f, The albumin. g, The chalaza. h, The yellow layers of yolk.
i, The white layers of yolk. k, The flask-shaped portion of white yolk. l, The
vitelline membrane.

The shell consists of several layers. Three are easily distinguishable: first,
an inner mammillary layer, consisting of minute conical deposits of
calcareous material; second, a middle spongy layer, composed of a thick
network of fibers; third, an outer delicate, cuticle-like structure. In certain
breeds of poultry a pigment may be added; for example, in ducks a pea
green, in turkeys a spotted brownish material, and in fowls pink and various
shades of brown. The egg shell is porous to admit the free exchange of air
during the process of incubation.
An average sized hen egg weighs about 2 ounces, of which 11 per cent. is
shell, 32 per cent. yolk, and 57 per cent. white. The principal chemical
constituents of the egg are as follows: ash, or mineral matter, 9 per cent.;
fat, or hydrocarbon, 9.3 per cent.; proteids, or nitrogenous matter, 11.9 per
cent.; and water, 65.5 per cent. There is apparently no constant proportion
of weight between the yolk and albumin. There is also a variation in the
weight of the shell due to its variation in thickness.

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In an examination of ten eggs of average size, the yolk constituted 31 per
cent. of the total weight of the egg.
The following is the result of the analysis of twelve eggs of average size.
This analysis included the shell and all other parts taken together.[6]
6. The analysis was made by D. M. McCarty, chemist, Animal Industry Division, North Carolina
Experiment Station.

Moisture 64.25 per cent.
Dry matter 35.75 per cent.

100.00 per cent.

Parts per hundred including shell

Protein 10.2500
Fat 10.6200
Phosphorus .3020
Calcium .6080
Magnesium .0985
Iron .0103
Sulphur .3950
Chlorine .1506
Potassium .0103
Sodium .2000

The Oviduct.—The three separate and distinct portions of the egg,
albumin, shell membranes, and the shell, are constructed in different parts
of the oviduct.
Location.—The oviduct of the hen extends along the left side of the
bodies of the vertebræ, and the roof of the pelvic cavity and lies dorsal to
the abdominal air-sac. It extends from the posterior border of the ovary and
empties into the cloaca (Fig. 56, No. 3 and 8) through a transverse slit.
Shape.—In a well-developed Plymouth Rock pullet, but one whose
reproductive organs have never become active, the oviduct is about 4½
inches long; in the fully developed and active state it is from 18 to 20 inches
long, and in a collapsed state about ½ inch in diameter. It is held in position
by two ligaments, a dorsal and a ventral (Fig. 55, B) to be described later.

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The oviduct is tortuous in its course, forming three principle convolutions
before reaching the cloaca, and like the ovarian mass, in its active state,
pushes the abdominal viscera downward and toward the right side.
Structure.—The oviduct consists of three coats: first, the serous, located
on the outside, which is a reflection of the peritoneum; second, the
muscular middle tunic; third, the mucous coat, which in a resting state is
thrown into folds.

Fig. 59.—The active oviduct of a hen
laid open. 1, The ovary. 2, The funnel. 3,
The albumin-secreting portion. 4, The
isthmus. 5, The shell=gland portion. 6,
The vagina. 7, The superior ligament. 8,
The inferior ligament.

Parts of the Oviduct.—The parts of the oviduct are as follows: the
funnel, the albumin-secreting portion, the isthmus, the shell-gland portion,
or uterus, and the vagina (Fig. 59).

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Fig. 60.—The mucous lining of the oviduct.

A. Transverse section of the oviduct wall in the region of the neck of the funnel
showing primary and secondary folding of the epithelium (after Surface).

B. Showing the type of gland cells of the funnel region.

C. Transverse section through the wall of the uterus showing the deep folds.

D. Section from the albumin-secreting portion showing the opening of a tubular
gland and also showing the character of the cells.

The funnel is the trumpet-shaped portion, the ostium tubæ abdominale,
whose mouth or fimbriated opening faces the ovary, and lies ventrally to
receive the ovum, or yolk, as it is discharged from the ovary. Its thin wall,
expanded in the anterior portion, is provided with fimbriæ-like projections.
This funnel-shaped portion soon converges to form a constricted portion.
This portion of the active oviduct is from 3 to 4 centimeters long. The
mucous membrane occurs in folds forming low longitudinal spiral ridges
(Fig. 60, A). The fimbriæ are continuous with the dorsal and the ventral
ligament of the oviduct; and from this point, where the ridges of the mucous
membrane are almost nil, they gradually increase in height as they extend
down the tube. These ridges are continued in those of the second, or
albumin-secreting portion (Fig. 60, D). At this point they increase in height
very rapidly. Here the bundles of muscular fibers of the middle coat are thin

Page 206

and distributed among bundles of connective tissue. The muscular fibers
consist of two layers, an outer longitudinal and an inner circular. At places
in this portion the inner bundles may be noted to extend longitudinally. In
embryological development the epithelial layer has an origin different from
the outer layers of the oviduct. In the fetal development the Müllerian duct
arises as a thickening along the Wolffian body just ventral to the gonad.
This Müllerian duct is at first a solid cord of cells. It later develops a lumen,
and grows posteriorly until it connects with the cloaca. At the time of this
posterior growth, mesenchyme cells migrate in from the surrounding tissue
and form a layer about the duct. From this layer of mesenchyme cells there
are developed the outer layers of the oviduct, which layers later develop the
muscular structure and the connective tissue. The epithelium and its
derivatives, which represent the glandular structures, are formed from the
walls of the old Müllerian duct. Thus the two sets of tissues, having
different origins, likewise have different functions. The epithelium is
concerned entirely with secretion, and the derivatives of the mesenchyme
are concerned with supporting and muscular function.
To summarize, six layers of tissue occur in the
funnel region, namely, an outer serous covering,
an outer longitudinal muscular layer, a layer of
connective tissue, an inner circular layer, a second
layer of connective tissue, and an inner mucous
layer. The mucous layer is made up of glands, as
follows. The unicellular glands occur between the
ciliated cells of the epithelium. These glands are
found only in the posterior half of this division of
the oviduct. The glandular grooves are made up of
an accumulation of gland cells at the bottom of the
grooves between the secondary folds of the
epithelium. These are found in all parts of this
division except the extreme posterior part. In the
posterior part we find the third type of glands, the
tubular variety. Fig. 60. A.—The
The second division of the oviduct, as stated mucous lining of the
above, is the albumin-secreting portion. The oviduct.
funnel division gradually merges into the second
portion. These two portions are distinguishable E. Section of the

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from each other. The walls of the albumin- epithelium from the
secreting portion are much thicker and the vagina showing
longitudinal ridges are higher. This section is the unicellular glands.
longest of the five divisions, measuring from 40 to
42 centimeters in length, or more than half the F. A section from the
length of the oviduct. The albumin division isthmus showing
terminates rather abruptly into the third division, opening of a tubule.
the isthmus (Fig. 59, A).
It is probable that the secretion of albumin is not confined to the cells of
the second division; yet we are safe in saying that the major portion is
formed here. The folds of mucous membrane in this division are thicker and
higher than in the funnel, due to their containing cells of the high columnar
type, and to the fuller development of the glands which are of the tubular
variety. The muscular layer is heavier, and therefore the muscular power to
force along the tubes’ contents is greater. In the formation of the mucous
folds we find, in transverse sections, that the central core is made up of
connective tissue which carries blood-vessels and nerve filaments, as in
other similar glandular structure. The epithelium contains glandular cells of
two varieties, namely, the ciliated, columnar variety, and the unicellular,
goblet variety (Fig. 36, No. B, 2). These two kinds of glandular cells are
rather evenly distributed throughout the epithelium of this section of the
oviduct. The unicellular gland cells are more numerous at the mouths of the
ducts leading from the tubular glands. The nuclei of the ciliated cells are
oval and lie near the middle of the cells or a trifle toward the base from the
middle. The protoplasm of the cells is finely granular. Strong cilia in
considerable number surmount each cell. In some cases the goblet or
mucous cells have pushed apart the ciliated cells, and their prolongations
extend farther than the surface of the ciliated cells. The nuclei of the goblet
cells are round, and lie nearer the proximal end than those of the ciliated
cells.
The third division of the oviduct, the isthmus, continues from the
albumin-secreting portion and terminates in the expanded portion called by
some anatomists, the uterus. Toward the posterior end of the albumin-
secreting portion the longitudinal folds of mucous membrane become
lower, making, at the juncture of this and the isthmus, a clear fine of
demarcation. For a distance of 2 or 3 centimeters the folds are low, after

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which they gradually become higher, but never reach the height or thickness
of those in the albumin-secreting portion.
The clear-cut line between the albumin-secreting portion and the isthmus
is partly due to a zone in which the long tubular glands are lacking. The
core of the folds of mucous membrane in this zone contain much more
connective tissue. The cells are both ciliated and unicellular. The rest of the
histological structure of the isthmus is the same as that of the albumin-
secreting portion.
The function of the isthmus is to secrete, or to form, the shell membrane,
the membrana testacea.
The fourth division of the oviduct is the uterus, or the shell-gland portion
(Fig. 60, C). There is no clear line of demarcation between the isthmus and
shell-gland portion, the walls gradually expanding. In this region the folds
of mucous membrane become leaf-like and of considerable length,
extending into the lumen, thus affording a greater cellular surface. The same
coats of the duct are present here as in other parts; but the outer longitudinal
muscular layer is thicker and possesses more strength. The quantity of
connective tissue is about the same. The glands are of a tubular type and the
same two varieties of epithelial cells are found here as elsewhere, namely,
the ciliated high columnar and the unicellular mucous variety.
In the active glandular cells of the shell-forming region the nuclei are
small, dark staining, and lie toward the center of the cell. The chromatin
granules and nucleoli take on a comparatively deep basic stain, but they do
not show the intense stain found in the albumin and the isthmus region. The
cytoplasm of the uterine tubular glands does not present as heavy a granular
appearance as that of the albumin portion. These cells are diffusely
granular, the granules appearing of one size and taking the stain faintly. The
function of this portion is to secrete, or form, the hard calcareous covering
which has been described at the beginning of this section.
The fifth division of the oviduct is the vagina. There is located, at the
juncture of the shell-gland portion with the vagina, a strong sphincter
muscle. The vagina is that constricted portion of the oviduct extending from
this muscle to the cloaca. The mucous membrane forms low narrow folds
with secondary folds, which appear continuous with those of the shell-gland
portion. The core of these folds is composed of connective tissue. The
vagina in the hen of average size measures from 12 to 13 centimeters long

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(Surface). The inner or circular muscular layer is well developed; it is much
thicker than in any other part of the oviduct. This extra development gives
the power necessary to successfully expel the egg. The outer longitudinal
layer is not so well developed; its bundles are scattered throughout the
connective-tissue layers. The egg is caused to move along in the oviduct by
a successive series of contractions of the circular muscular fibers posterior
to it. There are no tubular glands in this portion, but a simple layer of high
ciliated columnar epithelium, and some goblet, or mucous cells. The cells
on the surface generally are long and slender; in the grooves between the
mucous folds the cells are shortest, reaching their greatest length at the tops
of the folds.
The function of the vagina is the secretion, or formation, of the outer
shell cuticle commonly called the bloom, and also in certain breeds, as
indicated above, the tint.
The cloaca furnishes a passage way from the vagina to the external world
by way of the anus. The walls of the cloaca contain glands.
The Ligaments of the Oviduct.—It is held in position by two ligaments,
one dorsal and one ventral. The dorsal ligament of the oviduct is formed by
a double layer of peritoneum with a very small amount of connective tissue
interposed. The peritoneum is also reflected over the oviduct. The ventral
ligament of the oviduct is narrower than the dorsal, but is similarly
constructed. Both ligaments are rather veil-like in appearance. During the
first four or five months of the growth of the young female fowl the
development of the oviduct and its ligaments is in proportion to that of the
body. With the elongation that takes place about the time of functionation,
as described above, the ligaments enlarge in proportion to the enlargements
of the oviduct. The dorsal ligament maintains a line of attachment to the
body wall from the caudal end of the body cavity to the fourth thoracic rib.
The ventral ligament elongates only slightly during this developing period.
It becomes thicker and stronger and early develops a muscular coat. It also
grows in width except at the caudal end. At this point the ligament is simply
a mass of muscular tissue of the smooth or involuntary type. These
ligaments are fan-shaped.
The muscle fibers of the dorsal ligament of the laying hen, have their
origin in a line near the medial side of the dorsal margin. At this point the
bundles of fibers are quite thick, but are spread out thinly toward the margin

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of the oviduct. Frequent anastomoses are noted. The muscular fibers
become continuous with the circular ones of the oviduct.
The ventral ligament of the oviduct of the laying hen is largely a
muscular cord 3 to 6 centimeters in diameter. The caudal end is thicker,
becoming gradually thinner toward the anterior portion. The bundles of
muscular fibers extend toward the oviduct blending with the circular fibers
of that viscus. The ligaments terminate anteriorly in such a manner that they
aid in forming the serous ovarian pocket, which guides the yolk into the
fimbriated portion, or funnel, of the oviduct. The walls of the ovarian
pocket are formed by the left abdominal air-sac, a part of the intestine, and
the mesentery. The dorsal portion is formed by the roof of the abdominal
cavity, and the ventral portion is formed by the dorsal wall of the air-sac.
The medial, the anterior, and the lateral limit of the pocket are formed by a
fusion of the wall of the air-sac to the mesentery and to the body wall.
Posteriorly, the wall consists of the transverse part of the small intestine and
the caudal portion of the left cæcum with their attached mesentery.

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THE DUCTLESS GLANDS

These glands do not possess excretory ducts. They furnish materials
which are added to the blood or lymph as it passes through them. The
material from each gland is known as an internal secretion, or hormone.
Some of these secretions are powerful materials and influence profoundly
the body nutrition. The ductless glands are usually given as follows: the
spleen, the lymph glands, the pineal gland, the pituitary body, the thyroid
gland, the thymus gland, the adrenal glands, and the parathyroids. The
spleen, the pituitary, the pineal, and the lymph glands are described in other
sections.
The Thyroid Gland (Fig. 21, No. 16). Location.—The thyroid gland lies
on the ventral side of the carotis communis at a point where the carotis
communis touches the jugular vein, which is about the point of origin of the
vertebral artery.
Shape.—The thyroid gland is small, oval or somewhat roundish, and red
or rose-colored.
Structure.—The thyroid gland has a fibrous capsule, which sends into the
interior septa which divide it into acini. These acini are closed and contain a
fluid. The thyroid is a ductless gland. Short arteries from the carotis enter
this gland, and some large veins connect it with the jugular vein. The lymph
vessels which lie along the neck are closely connected with it and receive
twigs from the gland. The minute lymphatic capillary endings are found in
its septa and in its capsule. The acini are lined with a single or a double row
of cuboidal secreting cells. There are two kinds of cells, namely, secreting
and resting cells. The actively secreting cells secrete colloid.
The parathyroids consist of two small bodies attached to the lower pole
of the thyroid.

Page 212

The Thymus Gland (Fig. 47, No. 10).—The thymus gland is an organ of
fetal and early baby chickhood. It soon undergoes retrogressive changes
into fat and connective tissue. It is of epithelial origin, being formed in fetal
life from the entodermal cells of the dorsal end of the throat fissure.
Location.—The thymus gland lies anterior to the thyroid, the latter lying
the deeper.
Shape.—The thyroid consists of two lobes, which are united by
connective tissue, and appears as a loop-like acinous gland lying along the
neck and near the region of the bronchi and the jugular veins with fibrous
extensions toward the head.
Structure.—The gland lobes are divided into lobules, which consist of a
cortical and a medullary portion. The cortex consists of nodules of compact
lymphatic tissue similar to those found in the lymph glands. These occupy
the chambers formed by the septa of connective tissue. In the medulla there
are a number of spherical, or oval bodies composed of concentrically
arranged epithelial cells. These are known as Hassall’s corpuscles, and
represent only the remains of the original glandular epithelium. They are
characteristic of the thymus gland. The thymus appears to be a type of
lymph organ. Lymph vessels are rare; a few blood-vessels on the upper side
form capillary nets.
The Adrenal Gland (Fig. 54, F). Location.—The adrenal gland, often
called the suprarenal capsule, lies just anterior to the front part of the
anterior lobe of the kidney, adjacent to the testicles in the male and to the
ovary in the female. It is loosely attached by connective tissue to the
posterior aorta and to the vena cava.
Shape.—It is yellowish-brown or reddish-pink in color, small, and of
irregular formation.
Structure.—The adrenal gland consists of a cortical and a medullary
portion, although these two parts are not distinctly marked. The cortical
portion has columns which extend deeply into the gland, and the medullary
portion sends columns into the cortical portion. Therefore, the two
substances, lying side by side, form a cord-like structure.
It is probable that the cortical portion is derived from the ingrowths of the
peritoneum, and the medullary cords from the sympathetic ganglion.

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The cells are cylindrical or polygonal in shape, with an eccentric
substance between the columns. The cords, or columns, form between them,
elongated channels which extend into the interior of the gland and end as
blind or cæcal extremities. Large ganglionic nerve cells belonging to the
sympathetic system occur near the surface of the gland. The blood-vessels
are not well developed in the interior of the gland but are numerous and of
good size in the outer parts. Lymph vessels are also present.
Function.—The adrenals are ductless glands. They secrete an internal
secretion, or hormone, which influences the tonus of the blood-vessels. An
extract from these glands is called adrenalin.

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THE RESPIRATORY APPARATUS (Figs. 50 and
61, A)

Owen says: “Notwithstanding the extent and activities of the respiratory
function in birds, the organs subservient thereto manifest more of a reptilian
than of the mammalian type of formation.”
By the action of the respiratory organs certain chemical and physical
changes take place in the blood. The chief of these consists in absorption of
oxygen from, and giving off carbon dioxide to, the atmospheric air, the
former changes being necessary for the elaboration of the fluid, the latter
for the elimination of a substance which, if retained, would prove injurious.
The organs of respiration are invariably adapted to the wants of the animal
and the medium in which it lives.
In the bird, which breathes through its nose, the organs of respiration are
nostrils, nasal chambers, pharynx, superior larynx, trachea, inferior larynx,
bronchi, bronchial tubes, lungs, and air-sacs.
The Nostrils and the Nasal Chambers.—The nostrils of the bird open
externally by two small elliptical openings, which pierce the upper
mandible. Within each nasal chamber (Fig. 26, A) are three turbinated
laminæ, or turbinated bones. The inferior one is a simple fold adhering to
the lower and anterior part of the nasal septum. The middle turbinated bone
is the largest. It is of infundibular form, and adheres by its base to the
septum and externally to the side wall of the nose. It is convoluted with two
and a half turns. The superior bone, of bell shape, adheres superiorly to the
frontal bone. The internal turbinated bone extends toward the orbit; the
external terminates in a cul-de-sac behind the middle turbinal (Fig. 26, No.
A, 1 and 2, and G).

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The nostrils are separated by a partition which is partly bony and partly
cartilaginous. The posterior nares is represented by a long slit in the hard
palate.
The Pharynx and the Superior Larynx.—A transverse row of horny,
filiform papillæ marks the anterior border of the pharynx, where in other
animals the soft palate, or velum, is located. (For further description of the
pharynx see special chapter.)
The supero-posterior border of the larynx, at the juncture of the larynx
and the esophageal margin, is marked by a second transverse row of horny,
filiform papillæ, which point backward. There is no epiglottis. The superior
part of the larynx is pierced by an oval, slit-like opening, the glottis, which
is provided with two lips. These when brought together, tightly close the
glottis so that nothing can fall through into the larynx in the act of
deglutition. The margin, or rim, of this opening is called the rami glottis.
The glottis is controlled by two pair of muscles.
The superior surface of the larynx is somewhat triangular with the apex
directed forward. A few delicate, filiform papillæ are upon its surface. The
bird has, as already indicated, two larynxes, the superior larynx located at
the upper end of the trachea, and the inferior larynx at the bifurcation of the
trachea. The inner surface of the superior larynx is smooth and does not
contain vocal cords; it is in these animals simply a passage for air. It is
joined to the trachea inferiorly by a ligament, the crico-trachealis, and lies
at the base of the tongue supported by two cornua of the os hyoideum.
The cartilages forming the principal support of the superior larynx,
consist of four pieces, as follows: one unequal ventral piece, two side
pieces, and one unequal dorsal piece. The cartilaginous, flat, ventral cricoid,
early in the bird’s life, often becomes bony. The side pieces are separated
from it, only exceptionally fusing with it. The dorsal cricoid piece also often
becomes bony. The two arytenoid cartilages, joined with the cricoid
superiorly, are three-sided, and are united to each other in a sharp angle.
They form the superior opening of the superior larynx.
The Trachea.—The trachea is cylindrical and varies in length in
different kinds of birds in accordance with the length of the neck. It consists
of from 90 to 120 cartilaginous rings, complete with the exception of the
two uppermost, which rings are held together by intercartilaginous
ligaments. The tracheal rings are constructed of hyaline cartilage and the

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ligaments of fibrous tissue. It is lined with a mucous membrane covered by
columnar epithelium. The trachea is a passage for air alone and terminates
in the inferior larynx.
The Inferior Larynx.—The inferior larynx, called the true larynx
because it is the organ of voice, is located at the inferior end of the trachea
and the superior ends of the bronchi. By some anatomists this organ has
been called the larynx broncho-trachealis. The larynx is flattened laterally
in fowls. It contains two membranous folds, which in the production of
sound are caused to vibrate. These folds are half-moon shaped elastic
structures, located in the bony, arrowlike way, intero-inferiorly. These
structures are called the membrana tympana interna. In the duck this
inferior larynx is represented by a drum-like cartilaginous and bony
structure, called the bulla tympaniformis. This bulla is a resonant apparatus
which serves to strengthen the voice.
In song birds there is a double glottis, usually produced by a bony bar,
called the pessulus, or os transversale, which traverses the lower end of the
trachea from front to rear. It supports a thin membrane which ascends into
the tracheal area, and, terminating there by a free concave margin, is called
the membrana semi-lunaris. This is most developed in singing birds, and
being vibratile, forms an important part of their trilling vocal apparatus. The
air passes on each side of the membrana semi-lunaris and its sustaining
bone to and from the bronchi and lungs.
The last ring of the trachea usually expands as it descends, with its fore
and posterior parts produced, and the lower lateral borders concave; the
extremities of the pessulus, butts against the angle thus formed and expands
to be attached, also with the fore and posterior terminations of the first half
ring of the bronchus, strengthening and clamping together the upper part of
the vocal framework. The second bronchial half ring is flattened and curved
with the convexity outward, like the first, but is more movable. The third
half ring is less curved and further separated from the second, to the
extremities of which its own are connected by a ligament, and, for the
intervening extent, by a membrane; its inner surface supports the fibrous
cord, or fold, which forms the outer lip of the glottis of that side; it is
capable of rotary movements on its axis, and is an important agent in the
modulation of the voice. All these parts just described are bony.

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The Bronchi and the Lungs.—The bronchi, two in number, are
provided with only incomplete cartilaginous rings. They enter the inferior
face of the lungs, toward their anterior and middle thirds and break up into
primary bronchi, which give off at right angles, secondary bronchi, and
these latter in turn give off tertiary branches.

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Fig. 61.—The lung.

A. The outer surface of one lung. Note
the flattened oval shape. It is not divided
into lobes. 1, The bronchus. 2, Primary
tubules showing openings leading from
the primary tubules to the secondary
tubules. 3, Openings of two of the large
tubes into the diaphragmatic and
abdominal air-sacs.

B. Sectioned surface of lung. 1,
Secondary tubules. 2, Tertiary tubules.
3, Interlacing capillaries and air cells.

C. 1, Cavity of tubule. 2, Its lining
membrane supporting blood-vessels
with large areolæ. 3, Perforations in the
membrane at the orifices of the lobular
passage. 4, Interlobular space containing
the terminal branches of the pulmonary
vessels supplying the capillary plexus,
5, to the meshes of which air gets access
by the lobular passage.

The lungs occupy only about one-seventh of the thoracic space. They are
long, flattened, and oval, extending along each side of the spine from the

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second dorsal vertebra to the anterior end of the kidneys, and laterally to the
juncture of the vertebral with the sternal portions of the ribs. They present
two faces, a superior convex and an inferior concave; two borders, an
external and an internal; and two extremities, an anterior and a posterior
(Fig. 61). The convex surface is also called the dorsal, costal, or superior
face. It is moulded on the walls of the thorax and occupies a part of the
intercostal space, pushing the intercostal muscles outward. When the
surface of the lung is examined it is seen to be furrowed where the ribs
pressed during life. These furrows are as deep as the ribs are thick. The
sides of the lungs are covered with connective tissue which attaches them to
the costal walls.
The concave, or inferior, face also called the diaphragmatic or visceral
face is directed downward. The diaphragm separates it from the abdominal
viscera. The surface is covered by connective tissue which closely attaches
it to the diaphragm. It is perforated by the five tubules which bring the
posterior air-sac into communication with the lungs.
The borders of the lungs extend parallel to the long axis of the body. The
internal border is rectilinear, thick, and rounded. The external border is
convex, thin, and sharp.
The anterior extremity terminates in a sharp point which occupies a space
formed by the ribs externally and the inferior spines internally. The
posterior extremity is somewhat rounded and extends as far back as the
anterior border of the kidneys.
As soon as the bronchi enter the lungs they become broadened, the
cartilaginous rings disappear, and they continue as membranous channels
whose diameters gradually decrease, as they extend backward, to the point
where they terminate in the ostium caudale, at which point they are
surrounded by a cartilaginous ring. The ostium caudale brings the tubules
into communication with the ventral air-sacs.
Twelve air tubules have their origin from each common bronchus, or
trunk. Four are given off from the internal wall of the main bronchus by a
series of openings arranged in a row. Seven are given off from the external
wall by a second series similar to that of the first. The twelfth extends from
the inferior wall, and immediately takes a course downward and outward
and communicates with the posterior diaphragmatic air-sac. This may be
considered as the terminal branch of the trunk.

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All of these secondary canals, except the last, pass toward the periphery
of the lung. They divide and subdivide at the periphery, covering it with
their ramifications. The canals extending from the inner wall are distributed
to the inferior face of the lung. Those extending from the outer wall are
distributed to the outer face of the lung. The first constitute the
diaphragmatic and the second the costal bronchial tubes.
The four diaphragmatic bronchial tubes are numbered in the order in
which they are given off. The first is carried forward horizontally, the
second transversely inward, the third obliquely inward and backward, and
the fourth directly backward. They have, by some anatomists, been called
the anterior, the internal, and the posterior diaphragmatic bronchial tubes.
There are two posterior diaphragmatic bronchial tubes; the larger called the
great posterior, and the smaller, which passes directly backward, the small
posterior.
The costal bronchial tubes, seven in number, are numbered from the
front backward in the order they are given off. Parallel at their origin, and
side by side, like pipes of an organ, they soon spread out in fan-shape like
the preceding. They extend from their central origin to the periphery. The
first extends obliquely upward and inward to the anterior extremity of the
lung. All branches from this bronchus extend from its anterior wall. The
first branches are inflected to reach the external border of the lung. The
succeeding branches are directed forward and the last forward and inward.
They all meet those from the anterior diaphragmatic bronchus, but do not
anastomose with them.
The second, the third, and the fourth costal bronchi extend in a transverse
manner and ramify on the inner border of the lung.
The fifth and the sixth are directed toward the posterior extremity of the
lung. The seventh, very small, reaches this extremity, where it disappears.
The first costal bronchus is the largest; those following it gradually
become smaller. At their points of origin they adhere closely to the ribs.
They are all imperforate, which is a distinguishing feature from those
occupying the opposite face.
The canaliculi or tertiary tubules given off by these secondary bronchial
tubes do not differ greatly in caliber in the various parts. They are given off
at right angles from the pulmonary wall of each bronchus, and extend
perpendicularly into the lung substance. Thus we find three kinds of

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conduits, the primary, the secondary, and the peripheral, or tertiary. The first
are like the barbs of a feather on its shaft; and the second and
parenchymatous are implanted on the pulmonary walls of the first, like the
hairs of a brush on their common base. Thus instead of the branching of the
bronchi being dichrotomous, as in mammals, it is piniform.
The canaliculi, or finer tubules, communicate with one another. The inner
microscopic appearance of the canaliculi indicate that they are divided into
areola, which gives them a cellular aspect. These tertiary bronchi open on a
dense labyrinth of blood capillaries (Fig. 61, C). At this point the ciliated
epithelial cells give way to simple squamous epithelium.
Thus we find three kinds of bronchi, or their ramifications, as follows:
the primary, the secondary, and the tertiary.
The Air-sacs (Fig. 61, A).—The air-sacs are bladder-like structures
consisting of a delicate cellulo-serous membrane, an extension from the
bronchial tubes, in some places strengthened by an external envelope of
elastic fibrous tissue. Long thin blood-vessels are distributed in the
substance of these walls. They are branches from vessels of the general
circulation and not extensions from those of the lungs. No lymphatics have
been found in the air-sacs.

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Fig. 61, A.—Diagram of air-sacs and their location. 1, The proximal end of the
humerus. 2, The proximal end of the right clavicle. 3, The cervical air cell. 4,
The right coracoid bone. 5, The anterior thoracic air cell. 6, The right side of the
sternum. 7, The right side of the liver. 8, The peritoneum. 9, The right abdominal
air cell. 10, The coccyx. 11, The proximal end of the right femur. 12, The right
supero-posterior air-sac. 13, The right infero-posterior air-sac. 14, The right lung.
15, The axillary extension of the air-sac. 16, The obturator foramen. 17. The
pelvis.

These sacs do not communicate with each other and normally they are
not fully inflated. In some locations they extend into the bones and are in
communication with the extensions of the bronchial tubes. In fact, by some
anatomists they have been called “bladder-like, extra-pulmonary expansions
of the bronchial tubes, free from cartilage.” The air-sacs make the bird’s
body lighter, thus making long-continued flight possible. They are best
developed in those birds which fly most. There are four pairs of cells and
one single cell from which all other expansions and extensions are made.
These sacs are as follows: a single anterior thoracic, and, in pairs, cervical,
anterior diaphragmatic, posterior diaphragmatic, and abdominal.
The Anterior Thoracic Air-sac.—The anterior thoracic air-sac is located
above the clavicles and the interclavicular space, in the cavity of the thorax.
It is related superiorly with the trachea and the esophagus; laterally with the

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lungs and the cervical air-sacs; inferiorly with the sternum, the clavicle, and
the interclavicular aponeurosis; posteriorly with the heart and the anterior
diaphragmatic reservoir; and anteriorly with the integuments of the neck. It
contains the inferior larynx and the two primary bronchi, and large vascular
trunks from which are given off vessels supplying the neck and the wings.
Three prolongations, called subpectoral, subscapular, and middle, or
humeral, arise from the lateral walls of this air-sac. These prolongations
cross the walls of the thorax and pass around the articulation of the
shoulder.
The subpectoral prolongation extends from the thoracic reservoir by an
orifice situated behind the coracoid, and passes beneath the tendon of the
great pectoral muscle. When the pectoralis major contracts, this contraction
dilates the subjacent cell and draws into it a greater quantity of air.
The subscapular and the humeral prolongations communicate with the
thoracic air cell by a common opening situated behind the small adductor
muscle of the humerus. The subscapular prolongation, after leaving this
point, spreads under the scapular and the subscapular muscle, which it
separates from the ribs and corresponding intercostal muscles, and extends
in a longitudinal direction.
The humeral prolongation, smaller than the subscapular, occupies the
axilla, and is in shape triangular. It has from its summit into an infundibular
fossa, an extension which enters the canal of the humerus. The walls of this
cell form the lining of the air space in the humerus.
The thoracic air-sac thus possesses numerous membranous folds which
divide its cavity. The contiguous structures which it overlies, as the trachea,
the esophagus, the muscles of the inferior larynx, as well as the arteries and
veins, make its outer walls irregular. This orifice is dilated during
inspiration, by the contraction of the two first fasciculi of the diaphragm.
The Cervical Air-sacs.—The two cervical air-sacs are located just above
the thoracic air-sac at the inferior part of the neck and in front of the lungs.
They are cone-shaped with the base directed forward and the apex
backward. They are related superiorly with the cervical muscles, and
inferiorly with the thoracic air-sac from which they are separated by the
trachea, the esophagus, the pneumogastric nerve, and the jugular veins. The
walls touch each other internally, and form a median septum which includes
in its substance the two common carotid arteries. Externally they are related

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to the origin of the cervical nerves, to each of which they contribute a small
sheath. They surround the vertebral artery, and are connected with the
subcutaneous muscles and the skin. The summits communicate with the
anterior diaphragmatic bronchus. Prolongations extend from their bases
which conduct the air into all the vertebræ of the neck and the back, into all
the vertebral ribs, and into the spinal canal. Parallel with and adjacent to the
vertebral arteries, and lodged in the canals excavated in the transverse
processes of the cervical vertebræ, are two cervical prolongations, one on
each side, which extend to the cranium from the base of the cervical
reservoirs. From their sides, at the last six cervical vertebræ, are six
extensions in the form of diverticuli, which, lying against each other, pass
from each side into the muscles of the neck. They are surrounded by a thin
fibrous envelope, a continuation of the mucous lining of the sac, and
apparently form a canal in the inferior part of this region. These
prolongations are better developed in palmipedes than in chickens. On the
internal side of these prolongations, one or more foramina penetrate the
vertebral segment, which allow the extensions of the prolongations into the
spinal canal. Chauveau states that “as the medullary tissue is replaced by air
in the bones of birds, so is the subarachnoid fluid replaced by air around the
spinal cord.”
The prolongations extending from the cervical air-sacs, having entered
the thorax, terminate by passing into the first dorsal vertebra. After
permeating every part of this vertebra, it escapes by a lateral opening and
forms a small sac located between the first two ribs, near the origin of the
first dorsal nerve. From this sac an extension is given off, which enters the
second vertebral segment at the antero-lateral part; from this point it passes
back, forming a new air-sac between the second and third ribs. It now
passes in the same manner into the third vertebra and extends through the
third intercostal sac, and so on till the last dorsal vertebra has been served.
At the same time that these sacs receive the air from the vertebræ preceding
them, and transmit it to those which follow, they communicate it to all the
vertebral ribs. The aerial currents which leave the cervical air-sacs do not
communicate with those of the cranium. Experiments show that the cranial
bones have apparently no communication with the respiratory apparatus.
The Anterior Diaphragmatic Air-sac.—The two anterior diaphragmatic
or supero-posterior air-sacs are related with the lungs anteriorly, and with
the abdominal viscera posteriorly. Anteriorly also is the thoracic air-sac,

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posteriorly are the posterior diaphragmatic air-sacs, and laterally the ribs
and the intercostal muscles and internally is the esophagus. The lungs
communicate with these air-sacs through circular openings from the great
posterior diaphragmatic bronchus and frequently by a second opening from
this same tube. These are the only sacs which receive air from the lungs
through two openings.
The Posterior Diaphragmatic Air-sac.—The two posterior
diaphragmatic, or infero-posterior air-sacs are oval in shape and located
between the thoracic and the abdominal cavity. They are related anteriorly
with the anterior diaphragmatic air-sacs. These two sacs form a vertical
transverse partition. The posterior diaphragmatic air-sacs are related
posteriorly with the abdominal air-sacs from which they are separated by
the diaphragm. They are related below with the lateral parts of the sternum
and the sternal ribs, and externally with the ribs and the intercostal muscles.
These air-sacs communicate with the lungs through openings located in the
middle part of the external border of the lung, into the extremity of
voluminous bronchial tubes which follow the direction of the largest air
tubes.
The Abdominal Air-sacs.—The two abdominal air-sacs located on each
side of the abdominal cavity, when inflated with air, form enormous
bladder-like structures. They are related laterally with the abdominal wall
and internally with the abdominal viscera. The anterior extremities are in
communication with the mesobronchi and are somewhat inflected to pass
under the fibrous arches extending from the spine to the pelvis. Anteriorly
these sacs adjoin the diaphragm, the testes in the male, and ovary in the
female, and to the parietes of the abdomen and those of the pelvis. Below
and in front, they rest on a fibrous septum, which in all birds divides the
abdominal cavity into two smaller cavities: one anterior, representing the
abdomen and containing the liver; the other posterior, representing the
pelvis and containing the gizzard and the intestines. The anterior portion
overlies the posterior part of the lobes of the liver, the proventriculus, the
spleen, and the gizzard. The kidneys are located above these air-sacs.
Dorsal to the sacs is also a part of the intestines and in the female the
oviduct. The abdominal air-sacs are attached by a ligament-like structure in
their medial, their anterior, and their lateral margin. The posterior, the
dorsal, and the ventral margin are free. Mesially this attachment is to the
mesentery, connecting the left cæcum to the dorsal margin of the gizzard,

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and also to the mesentery of the proventriculus. The anterior attachment is
to the body wall and extends in front of the end of the ovary and the adrenal
glands. At the antero-lateral part of the body cavity the attachment extends
in a widening band along the lateral side of the ovary and of the oviduct, as
far back as the caudal margin of the sac. The lateral attachment is related to
the kidney, the dorsal ligament of the oviduct, and the abdominal wall.
Each of these abdominal sacs has three extensions: one suprarenal and
two femoral.
The suprarenal extension leaves the principal sac at the postero-external
part of the kidney, extends upward, and forward, and expands over the
surface of the kidney. At the internal border of the kidney, this prolongation
extends between the transverse processes of the sacral vertebræ, reaches a
height of the first dorsal vertebra, forms a triangular canal located above the
sacrum in the sacral channel, and is separated from its fellow by a series of
corresponding spinous processes.
The two femoral extensions, an anterior, small, and a posterior, large,
extend from the abdominal air-sac at the cotyloid cavity, leave the pelvis
through the bony passage occupied by the crural vessels, extend around the
coxo-femoral articulation, and terminate in a blind extremity. In some birds,
particularly in birds of prey and ostriches, there are prolongations extending
into the femur, entering through a foramen at the anterior part of the great
trochanter.
Summary of Bones Supplied by Each Air-sac.—The thoracic air-sac
communicates on each side of the thorax with twelve bones, including the
four sternal ribs. It supplies air to the clavicles, which are perforated at both
their extremities, and to the coracoids, which are perforated just below their
scapular extremity. The sternum is supplied through two series of openings,
the middle ones that conduct air into the sternal ridge and the lateral ones,
eight in number and very small, correspond to the intercostal spaces. The
sternal ribs are penetrated by small foramina at their inferior extremities.
From the subscapular extension the scapulæ receive air through one or two
foramina at their anterior extremity. The humeral prolongation supplies the
humerus through a foramen located at the upper edge of the humeral fossa,
at the infero-internal part of the articular head.
The cervical air-sac furnishes air to all the cervical vertebræ, to all the
dorsal vertebræ, and to all the vertebral ribs. The anterior parts of the

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vertebræ of the neck are supplied with air through the passage
accommodating the vertebral artery. The posterior parts of the vertebræ are
supplied by extensions from the interspinal canal. The first extensions
obtain entrance to the anterior segments by one or more openings of the
inner wall of the intertransverse canals; the median extensions penetrate the
posterior segments by two openings, a right and a left, situated on the inner
wall of those segments. The first dorsal vertebra is supplied with air in the
same manner, by the middle and the lateral canals of the neck. This air, after
passing through the first vertebra, leaves by a lateral exit to enter a small
air-sac. From this it passes into the superior part of the second vertebra,
escapes from this through its lower portion, to be received into a lateral sac,
and so on to the last dorsal vertebra. These sacs also supply the vertebral
ribs with air, which enters them by very small openings located on their
spinal extremities.
The diaphragmatic air-sacs do not have communications with the bones.
The abdominal air-sacs communicate with the sacrum, the coccygeal
vertebræ, the iliac bones, and the femurs. The air passing through the
sacrum, the coccyx, and the ilium comes directly from the suprarenal
extensions; the air which fills the femoral cavity comes from the femoral
extensions.
In some birds these air spaces are more greatly developed than in others.
The bones that are always aerated in all birds are the cervical and the dorsal
vertebræ, the sternum, and the humeri. Those aerated in some kinds only
are the furculum, the scapulæ, the vertebral and the sternal ribs, the sacrum,
the coccyx, and the femurs. Those that are never aerated are the bones of
the forearm, the hand, the leg, and the foot.
The service of air to the bones in most parts of the body by the air-sacs,
as just shown, is in special cases otherwise rendered. The Eustachian tubes
furnish air to the bones of the cranium and to the upper jaw; while the lower
jaw receives air from the pneumatic foramen situated upon each ramus
behind the tympanic articulation, and from an air cell which surrounds the
joint.
The cavities of the embryonic bones, which afterward become
pneumatic, are filled with marrow. Selenka states that the invasion of the
bones by the air is a late development, and that in the humerus this invasion
occurs after the twenty-second day in the life of the chick.

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Hunter and Compar, who have made extensive researches, consider the
function of the air-sacs as threefold.
First, the air-sacs are subsidiary respiratory organs, which aid in ridding
the blood of waste products and in taking in oxygen.
Second, they aid mechanically the actions of respiration in birds. During
the act of inspiration the sternum is depressed, the angle between the
vertebral and the sternal ribs is made less acute, and the thoracic cavity
proportionately enlarged; the air then rushes into the lungs and into the
thoracic receptacles, while those of the abdomen become flaccid. When the
sternum is raised, or approximated toward the spine, part of the air is
expelled from the lungs and the thoracic air-sac through the trachea, and
part is driven into the abdominal receptacles, which are thus alternately
enlarged and diminished with the expansion and the contraction of the
thorax. Hence the lungs, notwithstanding their fixed condition, are subject
to due compression through the medium of the contiguous air receptacles,
and are affected equally and regularly by every motion of the sternum and
of the ribs.
Third, they reduce decidedly the specific gravity of the whole body. This
must necessarily follow from the large spaces filled with air as well as from
the absence in the bones of marrow and other fluids. The air-sacs by their
position also render equilibrium more stable.

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ANGIOLOGY

The Circulatory Apparatus.—The circulatory apparatus consists of two tubular systems: the blood vascular
system and the lymphatic system.
The blood vascular system consists of the heart, the arteries, the veins, and the capillaries.
The heart is the central, propelling organ. The arteries form a series of efferent tubules, which, by branching,
constantly increase in number and decrease in caliber, and which serve to carry the blood from the heart to the
tissues. The capillaries are extensions from these latter tubules into which the arteries empty, and through the walls
of which the interchange of elements between the blood and the other tissues takes place. The veins form a system
of converging tubules which receive the blood from the capillaries, decrease in number and increase in size as they
approach the heart, and return the blood to that organ.
The lymphatic system consists of capillaries and veins alone. As in the blood system, the lymph capillaries
collect the effete material and pour it into the lymph veins, and these in turn, carry it to the large blood veins
adjacent to the heart.
Both these systems have one and the same continuous lining, which consists of a single layer of endothelial
cells. In the heart this lining is called the endocardium, and in the vessels, the endothelium. It forms a perfectly
smooth surface.

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THE HEART (Fig. 21, No. 7)

The heart of the domestic fowl is located in the median line of the thoracic cavity. It is more anterior and mesial
than in mammals. Its axis is parallel with the axis of the trunk. The lungs being confined to the dorsal part of the
trunk, the lower part of the heart is not surrounded by them, but extends backward, the apex resting in the anterior
part of the anterior median fissure of the liver.
The heart has the form of an acute cone (Fig. 50, No. 1), the apex of which is bluntly rounded.
The heart is surrounded by a sero-fibrous sac, the pericardium. This sac adheres to the cervical air reservoirs
anteriorly and to the diaphragmatic septum posteriorly. It is composed of two membranous layers: the parietal,
external, dense, and fibrous; and the visceral, internal, and serous. The pericardial sac has no direct attachment to
the heart, except at the upper extremity where it surrounds the large vessels emerging from it. The serous layer is
reflected over the outer portion of the heart, where it is called the epicardium. The function of the pericardium is to
prevent friction during the beating of the heart. It contains a small amount of serous fluid for perfect lubrication.
This fluid is called the liquor pericardii.
Internally the heart has four cavities: two auricles and two ventricles. The right ventricle is more crescent-
shaped than in solipedes, and in a manner envelops the left ventricle in front and to the right, though it does not
reach the point of the heart. The right auricle is larger than the left. The auriculo-ventricular valve is not tricuspid
as in mammals. This valve instead of being formed as usual by a membranous curtain, with margins retained by
cords fixed to the walls of the ventricles, is composed of a wide muscular leaf, which appears to be a portion of the
inner wall of the ventricle detached from the interventricular septum. This septum is convex; and the auriculo-
ventricular orifice is an oblique slit situated between it and the muscular valve in question; so that, when the heart
wall contracts at the systole, the valve is applied against this septum and closes the passage. The bicuspid, or
auriculo-ventricular valve of the left side usually has two segments, though occasionally there may be three. The
fossa ovalis is a depression behind the posterior semi-lunar valve in the septum of the heart. The membranous
septum closing the foramen ovale is complete and strong but thin and transparent. The right auricle receives the
blood from the two venæ cavæ coming from the anterior extremity, and from the posterior vena cava. These empty
into a sinus. The left auricle has two vessels, the pulmonary veins which bring blood to it from the lungs.

Structure of the Heart.—The heart is lined by a serous membrane, the endocardium, which is a continuation of
the endothelium of the blood-vessels. There are a few muscular pillars in the inner wall, called the columnæ carnæ.
To give the heart its pumping power, it is made up of contractile tissue, a specialized kind of muscle called heart
muscle. It is involuntary-striated and occupies an intermediate position, both morphologically and embryologically,
between smooth involuntary muscle and striated voluntary muscle (Fig. 74, No. 4). It, like striated voluntary
muscle, is both transversely and longitudinally striated. Heart muscle cells are short, thick cylinders, which are
joined end to end to form long fibers. By means of lateral branches the cells of one fiber anastomoses with cells of
adjacent fibers. Each cell of heart muscle contains one centrally located nucleus. There is no distinct sarcolemma,
but the sarcoplasm is more dense near the surface of the cell, which gives it the appearance of an enveloping cell
wall. There is a zone free from fibrillæ around the nucleus. The longitudinal fibrillæ, which make up the cell, are
held together by a cement-like substance.
The main mass of the heart wall, called myocardium, consists of the specialized muscular tissue just described.
The myocardium differs in thickness in different parts of the heart wall. It is thickest in the left ventricle and
thinnest in the auricles. The left ventricle forces the blood through the systemic circulation and hence must be
thicker to give it more power than is needed for the right ventricle, which forces the blood only through the lungs.
The auricles are thinnest of all; for they receive the blood and pass it only to the chambers below. The auricular
appendages at the base of the heart in fowls are not so well marked as in mammals. The auricular muscles consist
of an outer coat common to both auricles, the fibers of which are transverse and of an inner coat, independent for
each auricle, the fibers of which are longitudinal. Between the two coats, occur bundles of muscle the fibers of
which run in various directions. The disposition of the muscle tissue of the ventricles is much more complicated. It
is composed of several layers of fibers intricately interwoven.
The endocardium, covering the inner surface of the myocardium, forms a serous lining of all the chambers of
the heart. At the arterial and venous openings it is continuous with and similar in structure to the intima of the
vessels. The endocardium consists of two layers, an external layer closely attached to the myocardium and

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consisting of mixed fibers, including those of elastic tissue and smooth muscle cells; and an inner, single layer of
endothelial cells, spoken of above.
The heart is supplied with nutrient blood by the two coronary arteries, which are given off from the common
aorta just above the semi-lunar valves.
A right, or anterior, and a left, or posterior, coronary from their point of origin, turn in a ventral direction
between the root of the aorta and the pulmonary artery, the right going to the right coronary groove and the left to
the left coronary groove in the crown furrow. From here they send branches into the heart. The anterior, right,
coronary, or coronaria dextra, the larger, is given off from the inferior wall of the aorta. It divides into a ramus
superficialis and a ramus profundus. The ramus superficialis enters the crown furrow and divides into two or three
branches on the right heart wall. These branches extend to the apex of the heart. Twigs from this artery along its
course extend into the muscular wall reaching the posterior of the coronary groove where they anastomose with
those of the left coronary, the ramus profundus, and with other branches from the same artery. The ramus
profundus, larger than the preceding, gives off fine branches into the walls of the aorta and of the pulmonary
artery, then enters from behind into the right wall of the septum ventriculorum, extends into the apex of the heart,
and supplies the septum, or right inner chamber wall with the last branch, this breaking through the posterior wall
of the auricular appendage.
The posterior, left coronary, or coronaria sinistra, originates from the dorsal wall of the aorta, proceeds as one
branch on the upper surface of the left auricular appendix, and then extends between the left appendix and the
pulmonary artery to the ventral surface of the heart. On the left side it supplies the wall of the pulmonary artery
and gives off a ramus profundus. It sometimes divides into two parts and supplies the ventral wall of the right
chamber and then extends to the left wall of the septum medium. The rest of the coronaria sinistra enters into the
left crown furrow as the ramus superficialis, which provides the left and dorsal upper surface of the left chamber to
the apex. From this furrow it extends into the left chamber and the left appendage, and finally fuses with the ramus
superficialis of the coronaria dextra.

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THE BLOOD-VESSELS

The blood-vessels consist of arteries, veins and capillaries.
The Structure of the Capillaries and Arteries.—The capillaries are minute vessels which connect the
arterioles, or terminal arteries, with the venules, or terminal veins. They are only from 6 to 14 microns in diameter.
Their walls consist of a single layer of endothelial cells, which are somewhat elongated in the long axis of the
vessels. Their edges are serrated, and are united by a small amount of intercellular cement-like substance.
Capillaries branch without diminution in caliber, and these branches anastomose to form capillary networks, the
meshes of which differ in size and shape in different tissues and organs. The largest meshed networks occur in the
serous membranes and in the muscles; and the smallest occur in the glands, such as the liver.
The walls of the arteries are thick and stand open when empty, owing to the elastic tissue contained in their
walls, while the walls of the veins collapse when empty, owing to their containing a smaller amount of elastic
tissue. The arterial wall is provided with three coats: tunica intima, or inner coat; tunica media, or median coat;
and tunica adventitia, or outer coat.
The tunica intima consists of a single layer of endothelial cells, continuous with and similar to that forming the
walls of the capillaries. In passing from the capillaries to the arterioles, there is first a thin coat, or sheath-like
layer, of connective tissue around the outside of the endothelial tubes. Further along, isolated smooth muscle cells
arranged in a circular manner occur between the endothelial layer and the layer of connective tissue, this structure
forming vessels called precapillary arteries. Further along still, the muscle cells form a complete layer; in this
section the vessels are called arterioles and are made up of three coats: the inner endothelial, the middle muscular,
and the outer fibrous.
In arteries of medium size the intima consists of the endothelial layer, a layer of delicate white and elastic fibers,
connective-tissue cells, and the membrana elastica interna, or an outer layer, the elastic layer, of the intima.
The media consists of a thick coat of circularly arranged smooth muscle cells, its thickness depending largely
upon the size of the vessels. There is also a small amount of fibrillary connective tissue, which supports the muscle
cells. Elastic tissue is present in the media, the amount depending on the size of the vessel, the larger the vessel the
more elastic tissue there is present. In the large arteries coarse elastic fibers intermingle with the finer ones. When
much elastic tissue is present the muscle cells are separated into more or less well-defined groups.
The adventitia is composed of loose connective tissue with some elastic fibers. A few smooth muscle cells are
present, which, as are also the elastic fibers, are arranged longitudinally. The adventitia, blending with the
connective tissue surrounding the arteries, serves to anchor the vessels to the surrounding structure.
Structure of the Veins.—In many respects the walls of the veins resemble those of the arteries. The same three
coats exist and the same elements enter into their structure. The transition from capillary to small veins, and from
those to larger veins, is similar to the transition from the arteries to capillaries, in inverse order. The walls are not
so thick as those of arteries. The elastic tissue is much less in quantity and in smaller veins disappears. There is not
a clear line of demarcation between the intima and the media.
The veins of birds differ from those of mammals in that they have fewer valves. The valves are also less perfect,
and often permit a backward flow of blood.
The walls of the arteries and of the veins are supplied with nutrient blood-vessels. These are called the vasa
vasorum, or blood-vessels of the blood-vessel wall. They are mostly in the adventitia. They may arise from the
vessel to which they are distributed or take origin from an adjacent vessel. These small arteries supplying the
vessel coat after terminating into capillaries form small veins through which the blood, from the structure of the
vessel wall, is returned.
The walls of the blood-vessels are supplied with both medullated and non-medullated nerves. The non-
medullated nerve fibers are axones of the sympathetic neurones and control the caliber of the vessels. These fibers
are called the vasomotor nerves. They form plexuses in the adventitia, from which are given off branches which
penetrate the media and terminate on the muscle cells. The medullated nerves are the axones of the spinal nerves.
The larger fibers are found in the connective tissue outside the adventitia and give off branches to the media where
they divide repeatedly, lose their sheath, and terminate in the media and at times in the intima.

The Arterial Trunks

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The common aorta is short; it originates from the left ventricle (Fig. 61B, No. K, 14), and is guarded by three
semi-lunar valves. The aorta breaks through the pericardium just to the right of the pulmonary arteries in a ventral
direction; it then turns upward dorsally and to the right of the inferior bodies of the vertebræ. It is then directed
anteriorly, and dorsally to the right bronchus, between the right bronchus and the right lung. The right and the left
coronaries are given off from the common aorta; they have been discussed. There is next given off the left brachio-
cephalic or brachio-cephalic sinister artery (Fig. 61B, No. K, 10), which is just above the border of the base of the
heart. This artery passes upward and slightly forward, over the center of the inferior larynx. Just beyond this point
the subclavian artery is given off; this artery later becomes the axillary and the axillary the brachial artery. Then
there is given off the anterior and the posterior thoracic arteries; and finally, the pectoral, which supply the
pectoralis muscles and later terminate in the carotid, the vertebral, and the cervical arteries. The carotid artery
gives off an esophageal artery. The other arterial trunk given off from the common aorta is the right brachio-
cephalic or brachio-cephalic dexter (Fig. 61B, No. K, 18). The right brachio-cephalic artery gives off the
subclavian, which continues as the axillary, and continues as the brachial artery. There is given off the anterior and
the posterior thoracic, the right carotid (Fig. 61B, No. K, 11), the vertebral, and the dorsal. The last continues as the
cervical.

Fig. 61B.

K. The arterial trunks. 1, The middle sacral artery. 2, The hypogastric
artery. 3, The posterior mesenteric artery. 4, The ischiadic artery. 5, The
femoral artery. 6, The renal artery. 7, The left pectoral artery or thoracico
caudalis. 8, The left axillary artery. 9, The left carotid artery. 10, The left
brachio-cephalic artery. 11, The right carotid artery. 12, The right brachial
artery. 13, The right pectoral artery. 14, The common carotid artery. 15,
The posterior aorta. 16, The celiac axis. 17, The anterior mesenteric artery.
18, The right brachio-cephalic artery. 19, The auricular portion of the heart.
20, The ventricular portion of same. 21, Sterno-clavicular artery. 22, Anterior
thoracic.

L. The venous trunks. 1, The caudal vein. 2, The coccygeo-mesenteric vein. 3, The posterior mesenteric vein. 4, The
anterior mesenteric vein. 5, The gastro-duodenal vein. 6, The portal vein. 7, The hepatic vein. 8, The left anterior vena
cava. 9, The left pectoral vein. 10, The left brachial vein. 11, The left jugular vein. 12, The right jugular vein. 13, The right
brachial vein. 14, The right pectoral vein. 15, The right anterior vena cava. 16, The posterior vena cava. 17, The common
iliac vein. 18, The femoral vein. 19, The renal vein. 20, The internal iliac vein. 21, The hypogastric vein. 22, The auricular
portion of the heart. 23, The ventricular portion of same.

The pulmonary arterial trunk is given off from the conus arteriosus of the right ventricle. It is guarded at its
origin by three semi-lunar valves similar to those of the aorta. The trunk divides into two pulmonary arteries,
which are short, one called the pulmonalis dexter and the other the pulmonalis sinister. The former goes to the right
and the latter to the left lung. Each branch penetrates the lung near the bronchus. These arteries divide, or branch,

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similarly to the bronchi. Following the branchings of the bronchi, they finally terminate into the lung capillaries,
forming networks on the bronchi and the air-tube terminals.

BRANCHES OF THE BRACHIO-CEPHALIC ARTERY

( Thyroidea

( ( Cervicalis inferior

( Vertebralis ( Vertebralis anterior

( ( Vertebralis posterior

( ( Arteria cervicalis ascendens

( Bronchiales

( Truncus ( Inferior esophageal

( caroticus ( Subcutaneous colli

( ( ( Carotis cerebralis

( ( Carotis ( Cervicalis superior

( ( communis ( Occipitalis

( ( ( Carotis externa

( ( Spinalis anterior ( Basilaris ( Cerebelli inferior

Brachio-cephalic (

( ( Clavicularis

( ( Sterno-clavicularis ( Sternalis

( ( ( Acromialis

( (

Page 235

( ( ( Subscapularis

( ( ( ( Ulnaris

( Subclavia ( Axillaris ( Brachialis ( Brachialis profunda

( ( ( Radialis

( ( Humeralis ( Circumflex humeralis

( ( ( anterior

(

( ( Thoracica externa

( Thoracalis ( ( Arteria thoracica

( Thoracica inferior ( longa

(

( Mammaria interna

( Circumflex humeralis posterior

Brachialis profunda ( Collateral ulnaris

( Collateral radialis

The cord-like remnant of the ductus botalli, or embryonal connection between the lung arterial trunk and the
anterior aorta, has been observed but is rare in grown birds.
The arteries, the veins, and the lymphatic vessels of birds anastomose far more frequently than those of
mammals.

BRANCHES OF THE ARTERIA CAROTIS CEREBRALIS INTERNA

Page 236

( Occipitalis ( Occipitalis sublimis

( ( Occipitalis profunda ( Meningea

( ( Temporalis

( ( ( Rete t

( Ophthalmica ( Recurrent ophthalmicum ( Rete ethmoidalis

( externa ( Ethmoidali

( ( Plexus palpebralis

( ( Plexus alveolaris inferior

( ( Plexus muscularis

Carotis cerebralis ( Plexus temporalis ( Plexus lacrimalis

( ( Ramus ciliaris posticus

( ( Meningea media

(

( ( Sphenoidea (

( ( Spheno-maxillaris ( Ethmoidalis ( extern

( ( ( Ophthalmica ( (

( ( ( interna (

( Cerebralis ( (

( Ramus ( Sylviæ

( anterior ( Cerebralis profunda ( Choroid plexus

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( Arteria centralis retinæ

( Ramus posterior

BRANCHES OF THE ARTERIA CAROTIS EXTERNA

( Hyoidea

Carotis externa ( Laryngea superior

( Facialis

( Lingualis

BRANCHES OF THE ARTERIA CAROTIS FACIALIS

( Auricularis

Facialis ( Facialis interna ( Alveolaris inferior ( Mentalis

( Maxillaris interna

( Facialis externa

Page 238

Branches of the Carotid Trunk

The carotis communis artery springs from the carotid trunk of the brachio-cephalic. It is directed horizontally,
ascending to the ventral side of the neck. It then extends downward to the inferior median neck region. Just after
leaving its origin it gives off several small branches to the bronchi and to the esophagus, and extends toward the
head. The carotid lies on the thyroid gland and at this point touches the jugular vein (Fig. 21). At this point the
thyroid arteries are given off from the carotid trunk. The thyroid gland also receives blood from the bronchialis
artery.
Dorsalward and near the thyroid gland the carotid artery gives off a branch (the bronchialis) which accompanies
the recurrent laryngeal nerve, along the inferior larynx and the bronchi, and supplies the lung substance and that
part of the esophagus in this region.
The vertebral artery is given off from the carotid trunk, dorsalward to the thyroid gland, and on the left side.
The right vertebral artery may be given off from the brachialis dextra or right brachialis.
The inferior esophageal artery is given off from the ventral side of the carotid, supplies the esophagus, extends
then to the skin of the neck and to the trachea, is directed anteriorly toward the head and anastomoses with the
vertebral artery. This artery accompanies the vagus nerve and forms a collateral artery to the carotid and the
vertebral artery.
The subcutaneous colli springs from the carotid artery near the thyroid gland and communicates with the
inferior cervical artery, which, in turn springs from the vertebral artery.

The Common Carotid.—Near the last cervical vertebra the two carotid arteries occupy the same channel, to
which they are attached by fascia, and, lying close to the inferior surface of the bodies of the cervical vertebræ, are
covered by the colli muscles. Near the third or the fourth cervical vertebra, the two carotid arteries separate. Near
the atlas each carotid divides into the carotis cerebralis and carotis externa. Near this division the superior
cervical artery branches off. This latter artery extends down the neck in company with the pneumogastric nerve
and the jugular vein, supplies the skin and the neck muscles, and anastomoses with the inferior cervical artery and
the subcutaneous colli artery.
The occipital artery originates either from the carotis communis or sometimes from the superior cervical.

Branches of the Carotis Cerebralis

The branches of the carotis cerebralis are as follows:
1. The occipitalis (Fig. 72, No. 18), which in turn gives off, first, the occipitalis sublimis. The occipitalis
sublimis supplies the outer and the middle portion of the digastricus and the posterior mylo-hyoideus muscle. It
also gives off, second, the occipitalis profunda which supplies the inner portion of the digastricus muscle and
becomes the meningeal artery, which passes through the foramen vagi, entering the brain cavity, where it supplies
the coverings of the brain as far as the sella turcica. Superficial branches of this artery are distributed to the
muscles in the region of the atlas and anastomose with the vertebral artery.
2. The ophthalmica externa, which passes below the articulation of the quadrate bone, around the tympanic
cavity, enters the canalis caroticus, and passes into the cranial cavity. The ramus occipitalis, passing out of the
same foramen, again enters the diploë of the cranium; then after passing dorsally over the upper outer semicircular
canal of the ear, passes backward through the occipital bone.
The ophthalmica externa (Fig. 72, No. 9) forms a main trunk and gives off two branches: the temporal artery
and the recurrent ophthalmic. The recurrent ophthalmic gives off the rete temporalis, rete ethmoidalis, a branch to
the orbital gland, and finally anastomoses with its own branches and with those of the internal ophthalmic at the
olfactory foramen and aids in forming the ethmoidal artery. These arteries supply blood by giving off branches to

Page 239

the muscles of the eye, sclerotic coat, iris, choroid coat, and the ciliary bodies. It gives off another branch to
Harder’s gland, and finally anastomoses with the ethmoidalis.
3. The plexus temporalis, rete mirabile ophthalmicum, or wonderful network (Fig. 72, No. 8), is formed
between the second and the third trunk of the trigeminus nerve and the rete ophthalmicum.
Inferior to this is the alveolar plexus, which plexus accompanies the third branch of the trigeminus into the
lower jaw. Two main branches form this plexus, one coming from the carotis facialis, which anastomoses with the
alveolar artery.
The palpebral plexus lies between the trunks of the trigeminus, and supplies mainly the lower eyelid.
The plexus muscularis extends to the fifth portion of the temporal muscle.
The plexus lacrimalis forms on the posterior orbital wall on the ramus ethmoidalis and supplies the lacrimal
gland and the upper eyelid. It anastomoses with branches from the facial artery.
The ramus ciliaris posticus supplies the inferior rectus and the external rectus muscle of the eyeball. It
anastomoses with the ophthalmica externa.
The median meningeal artery passes through the foramen occupied by the second branch of the trigeminal
nerve. Passing into the cranial cavity, it supplies the dura mater. Before passing into this foramen, small branches
are given off, which supply the skin and the temporal muscle; and some branches anastomose with the superior
cervical and the ethmoidal arteries.

4. The Cerebral Artery.—Each cerebral artery enters the cranial cavity through the canalis caroticus located in
the sphenoid bone, passes forward medially from the cochlea, dorsally from the Eustachian tube, and passes
through a small canal which opens on the inner surface of the sella turcica. Originating in this foramen, the
sphenoid artery divides into two branches which anastomose with the pterygoidean and the pterygo-pharyngeal
artery and which supply the upper jaw and the throat regions.
The spheno-maxillaris artery supplies the gums.
The right and the left cerebral arteries unite at the sella turcica. After this union they divide again immediately
and pass to the base of the brain, where they give off twigs to the optic nerve, to the optic chiasm, and where also
is given off the arteria retinæ centralis. Passing posteriorly each cerebral artery gives off the ramus posterior, and
then passes to the side of the cerebellum.
The basilar artery, a continuation of the anterior spinal artery, is located ventrally and mesially to the
cerebellum. Laterally and inferiorly the basilar artery gives off the inferior cerebellar artery.
The ramus anterior is given off from the cerebralis artery and continues as the internal ophthalmic artery. The
ramus anterior also gives off the sylvian artery, which supplies the sides of the cerebrum and the middle brain. In
the fissure between the hemispheres and the optic thalamus is located the arteria cerebri profunda. This artery
passes along the median surface of the cerebrum and in its course supplies the adjacent parts. It enters into the
formation of the choroid plexus of the lateral ventricle.
The internal ophthalmic artery extends out of the cranial cavity, through the optic foramen, into the orbital
cavity. It passes upward along the interorbital wall and supplies the optic nerve, the trigeminus nerve trunk, and the
eye muscles, and dorsally anastomoses near the olfactory nerve with the rete ethmoidale and the external
ophthalmic artery, and continues as the ethmoidal artery.
The ethmoidal artery supplies the supra-orbital gland and the gland of Harder. It gives off twigs to the rete
ophthalmicum and other branches to the skin of the frontal region, where it anastomoses with branches of the
external facial artery. These branches in the frontal region are rather large. Large branches are given off to the
comb.
The arteria ethmoidalis externa originates in the nasal cavity from a division of the ethmoidal artery.
The external ethmoidal artery passes below the lacrimal bone, extends forward, supplies the walls of the nasal
cavity, and finally sends a branch anteriorly into the upper median portion of the jaw bone, and other branches to
the septum nasi and other parts of the nasal cavity.
There are frequent anastomoses between the ethmoidalis interna, the facialis, and the spheno-maxillary artery.
The internal ethmoidal artery supplies principally the posterior turbinated bones and septum nasi.

Branches of the External Carotid Artery

Page 240

Branches from the external carotid and the facial artery supply the tongue and its muscles, the larynx, the lower
jaw bone, the gums, and the upper lateral facial region.
The external carotid (Fig. 62, No. A, 8) gives off the following branches:
First, the hyoid artery (Fig. 72, No. 12) which supplies the inner portion of the depressor mandibular and also
the cornua of the os hyoideum, and extends to the tip of the tongue.
Second, the superior laryngeal artery (Fig. 72, No. 16) which supplies the sterno-brachialis and gives off
branches which extend downward to the trachea and to the esophagus. The main artery passes along the left side of
the esophagus and anastomoses with branches of the inferior esophageal, forming collateral circulation in that
region.

Fig. 62.

A. Blood-vessels of the head. 1, The cerebellum. 2. The
cerebrum. 3, The semicircular canals. 4, Sinus occipitalis
superior. 5, Sinus temporalis sphenoideus. 6, Sinus
transversus dexter. 7, Superior esophageal artery. 8, Carotis
externus. 9, Lingual artery. 10, Sinus longitudinalis.

B. Veins of the antero-inferior part of the head and neck. 1,
The right carotid artery. 2, The left carotid artery. 3, Vena
jugularis dexter. 4, Vena vertebralis dexter. 5, Transverse
vein. 6, Vena cephalica dexter anterior. 7, Vena lingualis. 8,
Vena cephalica posterior. 9, Vena facialis externa dexter. 10,
Vena infrapalatina. 11, Posterior nares. 12, Vena facialis
interna. 13, Vena facialis externa sinister.

C. The brain. 1, Medulla oblongata. 2, Cerebellum. 3, Optic
lobe. 4, Cerebrum. 5, Longitudinal fissure. 6, Transverse
fissure. 7, Olfactory nerve. 8, Optic nerve. 9, Optic
commissure. 10, Motor oculi. 11, Patheticus. 12, Trigeminal,
or trifacialis. 13, Abducens. 14, Facialis. 15, Auditory, or
acousticus. 16, Glosso-pharyngeus. 17, Pneumogastric. 18,
Spinal accessory. 19, Hypoglossus. 20, Hypophysis. 21, Crus
cerebri. 22, Ganglion on superior nerve trunk. 23, Spinal
cord. 24, A pair of spinal nerves.

Third, the lingualis artery (Fig. 62, No. A, 9) which lies between the mylo-hyoideus and the posterior part of
the hyoid bone. It supplies the tongue muscles. It passes to the median surface of the lower jaw bone, where are
given off small branches which enter the jaw and anastomose with the inferior alveolar artery.
Fourth, the Facial Artery.—The facial artery divides into the following branches:

Page 241

The auricular artery is given off near the articulation of the os quadratum with the os zygomaticum. It is located
at the outer auditory canal, and its branches are distributed to the parotid region and to the depressor mandibular,
or digastricus, muscle.
The external facial artery is located between the os quadratum and the masseter muscle. It gives off a branch to
the lower jaw bone and to the skin of that region, and then passes to the lacrimal bone and supplies branches to the
commissure of the mouth, the auditory canal, the masseter muscle, the three eyelids (upper and lower eyelids and
the membrana nictitans), the nose cavity, and the skin in the frontal region. It communicates on the other side with
the ethmoidal artery.
The internal facial artery passes over and through the os pterygoideum, supplies all the jaw muscles, and is
continued as the inferior alveolar artery.
The inferior alveolar artery enters the canal of the lower jaw bone along with the mandibular nerve. It is finally
continued as the mental artery, leaving the canal, and passing to the outer jaw surface.
The facialis continues as the internal maxillary artery.
The internal maxillary artery (Fig. 72, No. 15) supplies the pterygoid muscle, the upper part of the pharynx, the
commissure of the mouth, the salivary gland region, the gums, and finally anastomoses with branches of the
spheno-maxillaris artery.

Branches of the Vertebral Artery

The vertebral artery is given off, dorsally near the thyroid gland, from the carotis communis or from the carotid
trunk. The vertebral artery passes horizontally and dorsally into the canals formed in the transverse processes of
the cervical vertebræ. After it leaves the carotid, it is divided into anterior and posterior branches.
The posterior vertebral artery passes in the canals of the transverse processes of the fifth or sixth dorsal
vertebra. It sends branches into the vertebræ, into the spinal canal, and into the intercostal muscles between the ribs
and anastomoses with the intercostal arteries.
The anterior vertebral artery is larger than the posterior. It extends laterally along the side of the neck in the
foramen of the transverse processes of the cervical vertebræ, and lies along the course of the inferior vertebral vein
and the deep imbedded trunk of the sympathetic nerve. It continues to the head. In its passage it gives off to each
vertebral segment a dorsal and a ventral branch. Twigs from these branches pass into the bodies of the vertebræ
and the spinal canal, giving nutriment to the bony structure and to the spinal cord and its coverings. Other twigs
are distributed to the muscles of the neck and some finally anastomose with branches of the carotis communis.
This artery, reaching the head, gives off a long anastomosing branch which passes between the atlas and posterior
part of the occipital bone and joins the ramus profundus and the occipital artery, thus again communicating with
the carotid artery. The remainder of the vertebral artery is small and passes through the foramen magnum into the
cranial cavity where it anastomoses with terminal branches of the cerebral artery. At the base of the neck and
before the vertebral artery enters the canal of the cervical vertebræ, it gives off the arteria cervicalis ascendens,
superior artery of the crop (Fig. 73, No. 18) which branches out on the upper surface of the crop is also distributed
to the neck muscles, and later subdivides into the transverse cervical arteries which supply the skin and the
muscles of the base of the neck, and the shoulder region.
On the ventral side of the neck there are given off two subvertebral carotid arterial branches. They lie in a
shallow furrow on the ventral side of the cervical vertebræ and close to the median line.

Branches of the Subclavian Artery

The subclavian artery (Fig. 20, No. 13; Fig. 73, No. 11) gives off the following branches:

1. Sterno-clavicularis (Fig. 73, No. 9) which originates on the upper part of the subclavia, between the carotid
artery and external thoracic (Fig. 73, No. 3), divides into many branches. The sterno-clavicularis gives off the
sternal artery, which enters by the side of the supra-coracoid muscle and the anterior rim of the sternum. It is
distributed to the inner surface and over the air-sac. Another outside branch passes the posterior end of the crista
sterna and supplies the large breast muscles.

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The clavicular artery (Fig. 73, No. 8) accompanies the clavicle to the shoulder-joint.
The acromial artery is given off from the sterno-clavicularis on the ligament near the shoulder-joint.
2. The thoracic artery branches from the subclavian artery (Fig. 70, No. 4). The thoracic artery gives off the
following branches:
The internal mammary, or internal thoracic artery (Fig. 73, No. 16) arises on the inner side of the sternum and
extends downward and backward, giving nutrient branches to the anterior vena cava and to the diaphragm. At the
point of the costo-sternal muscle it divides into an inner and an outer branch.
The inner branch supplies the costo-sternal muscle and extends along the ribs and along their juncture with the
breast-bone. It finally extends posteriorly, giving numerous branches to the abdominal muscles. The outer branch
is distributed in a similar manner, giving off branches to the diaphragm and to the abdominal muscles, and
anastomoses, on the surface of the abdominal muscles, with the epigastric artery.
The external thoracic artery (Fig. 73, No. 3), ramus superior, supplies principally the large breast muscles.
The inferior thoracic artery, external ramus inferior, passes along the outside of the pectoralis major muscle,
extends downward, and gives off the arteria thoracica longa (subcutaneous thoracic). This latter artery supplies the
skin of the breast region. Other branches are given off to the muscles of the breast and to the skin of the region,
and some finally anastomose with the branches of the sternal artery.
3. The axillary artery (Fig. 73, No. 12) extends out of the thoracic cavity along with the brachial nerve plexus.
It gives off the subscapularis which supplies the muscles of the scapular region. The axillary artery terminates as
the brachialis which passes between the biceps brachii and anconeus muscles downward along the humeral shaft.
It gives off the anterior humeral circumflex artery and the brachialis profunda artery (Fig. 68, No. 3). It gives off
near the elbow-joint the ulnar and radial arteries.
The anterior circumflex humeral artery passes through the short head of the biceps and gives off a branch to the
biceps muscle, supplying the insertional part of the breast muscles.

Branches of the Brachialis Profunda

The brachialis profunda artery (Fig. 68, No. 3) continues as the posterior circumflex humeral artery. This artery
supplies the muscles of the posterior part of the humerus, the skin of the wing, and the muscles of the brachial
region. The trunk of the arteria brachii profunda passes downward along the anconeus muscle, supplying that
muscle and giving off the collateral ulnar artery. On the ulnar olecranon it anastomoses with the recurrent ulnar,
thus establishing, at this region, collateral circulation. The rest of the brachialis sends branches to the biceps
muscle and to the skin of the upper arm, and finally gives off the arteria collateralis radialis, which supplies the
condylo-ulnaris. It then anastomoses with the end branches of the recurrent radialis artery.
The radial artery (Fig. 67, No. 4) passes downward on the outer rim of the forearm. It continues down to the
carpal region, where it supplies the muscles and the skin of the carpal region it gives off the recurrent radial, which
passes on the middle finger and finally anastomoses with the collateral radialis artery.
The ulnar artery (Fig. 68, No. 6 and 9) passes downward on the inner surface of the ulna to the carpal region
where it gives off a branch to the wing plexus and divides into two branches, the smaller branch supplying the
thumb (Fig. 68, No. 7). This branch passes down the radial side of the middle finger to the last joint of the second
finger. The larger (Fig. 68, No. 8) lies between the second and the third finger bones, and passes through a slit
between these two bones to the flexor side of the hand and extends to the last finger-joint, supplying the structures
in the region. The ulnar artery gives off a small arterial twig to the papilla of each large wing feather (Fig. 67, No.
6).
The recurrent ulnar passes backward to the olecranon of the ulna and supplies the muscles, the skin, the
feathers, and other structures of the region, and terminates in end collateral ulnar branches (Fig. 67, No. 5).

BRANCHES OF THE POSTERIOR AORTA[7]

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( Esophageal

( Intercostales

( Dorsal

( Lumbars

( Spermatics

( Renals

( Ovarian

( Celiac ( Recurrent esophageal

( axis ( Recurrent intestinalis ( Recurrent ilio-colicus

( ( Posterior or recurrent sinister ( Renalis

( ( Anterior or recurrent dexter ( Splenics

( ( ( Hepatic

( ( Hepatica dextra ( Gastric

(

Posterior ( Sacralis media ( Coccygeæ laterales

aorta ( ( Coccygea media ( Coccygeæ laterales

(

( Anterior mesenteric ( Recurrent ilio-celiacus

( ( Recurrent superior hemorrhoidal

( Posterior mesenteric ( Median hemorrhoidal

( ( Recurrent renalis

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( ( Tibialis postica

( Ischiadica ( Tibialis antica ( Peroneal ( Anterior tibial plexus

( ( Arteria ovarialis

( Pudenda communis ( Renalis

( ( Hemorrhoidalis intima

( ( Pudenda externa

(

( Crural ( Internal pelvic (umbilical)

( (External iliac) ( Circumflex femoris

( ( Femoralis

7. Nomenclature used by Bronn.
The posterior aorta (Fig. 63, No. 2) passes backward along the inferior part of the bodies of the dorsal and
lumbo-sacral vertebræ. In the thoracic cavity it lies dorsal to the esophagus. It gives branches (esophageal) only to
the esophagus during its passage as far as the seventh dorsal vertebra. Following this point there are given of
several pairs of arteries which divide into a superior and an inferior branch. The superior branch extends upward
and anastomoses with branches of the vertebral artery and other twigs coming from the intercostal arteries. These
latter arteries given off are small dorsal arteries. The inferior branches extend downward between the ribs and
supply the intercostal muscles. The intercostal arteries do not take their origin from the aorta in numerous and
regular branches as in mammals; they consist originally of but few vessels, which are multiplied by anastomoses
with each other and with the arteries which come out of the spinal canal. An arterial plexus is thus formed around
the head of each rib, from which a vessel is sent to each of the intercostal muscles and ribs and are continued into
the muscles upon the outside of the body and its integuments. The anastomosis of the intercostal arteries round the
ribs is similar to the plexus, which is produced by the great sympathetic nerve in the same location. The lumbar
arteries are given off farther posteriorly and along the lumbar region. The lumbar, like the dorsal branches are
given off in pairs. These arterial branches pass along the thigh and the upper sacral vertebral region, and supply
those parts. Ventrally they are covered by the kidneys and pass into the abdominal muscles. The posterior aorta
gives off the spermatic arteries and the ovarian artery. In the male the former supply the testes. The ovarian artery
of the female gives off a twig to each calyx containing an ovum. Each calyx is voluminously supplied with blood.
Next the renal arteries are given off to the kidneys.

Page 245

Fig. 63.—The vascular system injected. 1, The heart. 2, The posterior aorta. 3, The right brachio-cephalic artery. 4, The
left brachio-cephalic artery. 5, The anterior mesenteric artery showing its many branches and anastomoses near and on the
intestines. It is accompanied by branches of the mesenteric vein. 6, The rectal branch of the posterior mesenteric artery. 7,
The duodenal loop and pancreas showing the pancreatic artery. 8, The anus. 9, The cloaca. 10, The liver. 11, The lungs. 12,
The right subclavian artery. 13, The right carotid artery. 14, The right anterior vena cava. 15, The subclavian vein. 16, The
right jugular vein. 17, The carotid trunk. 18, The posterior vena cava.

Fig. 64.—The splanchnic arteries, veins and nerves. 1, A
portion of the left testes. 2, Adrenal gland. 3, Anterior lobe of
kidney. 4, Heart. 5, Liver. 6, Second portion of the
esophagus. 7, Proventriculus. 8, Gizzard. 9, Spleen. 10,
Duodenal loop. 11, Pancreas. 12, Blind extremity of cæcum.
13, Floating portion of small intestine. 14, Rectum. 15,
Cloaca. 16, Anus. 17, Celiac axis. 18, Ureter. 19, Vas
deferens. 20, Recurrent sinister artery. 21, Anterior recurrent
dexter artery. 22, Arteria hepatica dextra. 23, Recurrent
esophageal artery. 24, Recurrent intestinalis artery. 25, Ilio-
colicus artery. 26, Anterior mesenteric artery. 27, Recurrent
branches of the same. 28, Ilio-cœliacus artery. 29, Recurrent
superior hemorrhoidal artery. 30, Posterior mesenteric artery.
31, Crural arteries. 32, Sacralis media artery. 33, Recurrent
renalis. 34, Middle renal lobe. 35, Posterior renal lobe. 36,
Vena mesentericus communis. 37, Vena hemorrhoidalis. 38,
Vena pancreatico-duodenalis. 39, Vena proventriculo-
leinealis. 40, Vena portalis dextra. 41, Ischiadic nerve. 42,
Thoracic sympathetic trunk. 43, Anterior splanchnic plexus.
44, Spinal nerves. 45, Posterior splanchnic nerve plexus. 46,
Intestinal nerve trunk. 47, Vena renalis magna.

The celiac axis (Fig. 64, No. 17) originates near the seventh sternal vertebra and to the right of the esophagus,
breaks through the diaphragm, and, near this point, gives off a recurrent esophageal (Fig. 64, No. 23). The celiac

Page 246

axis gives off three main branches: The anterior or recurrent dexter, the posterior or recurrent sinister, the recurrent
intestinalis, all of which lie to the right of the spleen, under the left lobe of the liver, and along the left side of the
stomach. The recurrent sinister (Fig. 64, No. 20) gives arterial branches to the proventriculus, the gizzard, the
pyloris, and the left lobe of the liver. The anterior or recurrent dexter (Fig. 64, No. 21) gives off a renal artery and
from four to six splenic arteries.
The recurrent intestinalis artery (Fig. 64, No. 24) arises on the posterior of the stomach within the duodenal
loop, and supplies the duodenum and the pancreas (Fig. 63, No. 7). It gives off a branch, called the recurrent ilio-
colicus (Fig. 64, No. 25), which supplies the large intestines, including the cæca.
The arteria hepatica dextra (Fig. 64, No. 22) is a branch from the celiac axial trunk. It gives several branches to
the right lobe of the liver and to the gall-bladder. The gastric branches pass to the muscles of the stomach. The
anterior and posterior recurrent branches often anastomose.
The anterior mesenteric artery (Fig. 63, No. 5; Fig. 64, No. 26) originates from the posterior aorta near the
generative glands. It is directed downward, and divides into many branches which pass in the mesentery toward
the intestines. Recurrent branches (Fig. 64, No. 27) are given off, which anastomose, forming mesenteric arches.
From these arches are given off branches which supply the intestinal walls.
The anterior mesenteric artery gives off the recurrent ilio-celiacus (Fig. 64, No. 28) which is distributed to the
cæca; other of its branches are distributed to the small intestine.
The anterior mesenteric artery extends along the small intestine and ends in the recurrent superior hemorrhoidal
arteries (Fig. 64, No. 29) which anastomoses on the surface of the rectum with a branch of the posterior
mesenteric artery.
Branches from the anterior mesenteric artery also anastomose with branches of the celiac axis.
The posterior mesenteric artery (Fig. 64, No. 30) is given off from the posterior aorta posterior to the origin of
the anterior mesenteric and near the arteries of the thigh and is distributed to the lesser mesentery supplying the
large intestine. Branches of the superior hemorrhoidal arteries anastomose with branches of the posterior
mesenteric artery. Branches from this source are called the median hemorrhoidal (Fig. 63, No. 6).
The posterior mesenteric artery (Fig. 64, No. 30) also gives off a long branch to the cæca. Branches of the
posterior mesenteric artery anastomose with branches of the anterior mesenteric.
The crural arteries (Fig. 64, No. 31) are given off in a pair from the posterior aorta. They pass through the
mass of the lobes of the kidneys, at about the median region, and extend out of the pelvic cavity in front of the
spine and ilio-pubic ligament.

Fig. 65.—Blood-vessels and nerves of the hind extremity. Inside view of leg. 1, Ischiadic nerve. 2, Ischiadic artery. 3,
Posterior tibial vein. 4, Vena metatarsa dorsalis interna. 5, Vena metatarsalis plantaris profunda. 6, Vena cruralis. 7, Vena
metatarsalis interna, vena magna. 8, Vena tibialis postica. 9, Vena metatarsa magna. 10, Nerves of the toes. 11, Vena
metatarsalis dorsalis profunda.

The crural, or the external iliac artery, is divided into three branches as follows:

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First, the internal pelvic, or umbilical artery, is given off just as the cruralis leaves the pelvic cavity. It passes, as
a long vessel, on the inner surface of the lumbo-sacral bones and supplies the obturator internus muscle and
extends into the umbilical region. It gives off branches to the abdominal muscles, and, in the female, a branch is
distributed to the ligament of the oviduct.
Second, the arteria circumflex femoris, which passes between the sartorius and vastus internus and extends
dorsalward, supplies the sartorius muscle, the vasti muscles, and the ilio-trochanteric region.
Third, the femoral artery, which passes beside the vena cruralis and extends down the posterior surface of the
thigh to the knee-joint, supplies the upper thigh muscles with the exception of the adductor muscles.

Fig. 66.—Blood-vessels and nerves of the posterior extremity. Outside view. 1, Anterior tibial artery. 2, Metatarsal artery.
3, Digital arteries. 4, Vena cutaneous crurus. 5, Ischiadic artery. 6, Vena cruralis. 7, Lateral cutaneous branch of the
ischiadic nerve.

Fig. 67.—Blood-vessels and nerves of the fore limb. Outside view. 1, Median nerve. 3, Ulnar nerve. 4, Radial artery. 5,
Recurrent ulnaris artery. 6, Twigs of ulnar artery to wing feathers.

The ischiadic artery (Fig. 69, No. 9) forms the main artery of the posterior extremity. This artery, the largest
vessel of that region, is given off from the posterior aorta and passes ventrally over and between two of the main
lobes of the kidney. The continuation of the posterior aorta is called the sacralis media (Fig. 64, No. 32). The
ischiadic artery gives off a recurrent renalis on the posterior lobe of the kidney (Fig. 64, No. 33). On the left side it
gives off a branch to the oviduct and to the ligament of the oviduct. The main trunk leaves the cavity with the
ischiadic nerve (Fig. 65, No. 1) through a foramen formed by the os ilium and the os ischium. It sends branches
into the adductor muscles of the upper and the lower thigh. It gives off anastomotic branches which unite with
those from the femoral artery. At the flexure of the knee-joint it gives off two branches to that region (Fig. 69, No.

Page 248

10). It gives off another branch to the gastrocnemius muscle and one to the flexor perforans digitorum. It
terminates in the anterior and posterior tibial arteries.

Fig. 68.—Blood-vessels and nerves of the fore limb. Inside view. 1, Vena humeri profunda. 2, Brachialis longus inferior. 3,
Brachialis profunda. 4, Radial artery. 6, Ulnar artery. 7, Ulnar arterial branch to thumb. 8, Digital branch of ulnar artery. 9,
Ulnar artery.

The first, the tibialis postica (Fig. 69, No. 12) passes between the gastrocnemius and the deep flexors giving off
branches in its course to the skin and to other parts, and disappears shortly below the intertarsal joint.
The second, the tibialis antica (Fig. 66, No. 1; Fig. 69, No. 11), is often the larger of the two arteries. The
anterior tibial artery gives off branches to the knee-joint and to adjacent structures. It gives a large branch to the
head of the gastrocnemius muscle. It passes to the posterior surface of the tibial head and gives off the peroneal
artery, which passes through the membrana interossea located between the tibia and fibula giving branches to the
anterior side of the membrane of the patellar region of the knee-joint. It gives branches to the anterior side of the
lower thigh and finally terminates subcutaneously in the anterior tibial plexus.
The main portion of the anterior tibial artery passes downward along the posterior surface of the membrane
located between the tibia and fibula, and sends branches for the flexor digitorum communis et profundus. It then
breaks through the membrane, reaches the anterior side and there communicates with the anterior tibial plexus. It
gives off branches to the muscles on the anterior side of the lower thigh and the skin, and passes between the outer
and the middle malleolus of the tarsal bones. It passes to the plantar surface and divides between the toes. In
addition to the plantar branches there are given off dorsal branches between the third and the fourth toes. These
branches form the direct continuation of the dorsal vessels of the anterior tibial plexus.

Page 249

Fig. 69.—Blood-vessels and nerves of the femoro-tibial region. A section of the tibia removed.

A. Veins, arteries and nerves dissected as in B.

B. V, Vein. A, Artery. N, Nerve. 1, Vena poplitealis. 2, The three veins forming the vena poplitealis. 3, Vena femoris interna
profunda. 4, Vena femoris anterior. 5, Vena cruralis. 6, Vena cutanea abdominalis femoralis. 7, Vena cutaneous cruralis. 8,
Deep vein of the knee-joint. 9, Ischiadic artery. 10, Branches of ischiadic artery to flexure of knee. 11, Anterior tibial
artery. 12, Posterior tibial artery. 13, Ischiadic nerve. 14, Trunk (a branch of the ischiadic) which gives off the superficialis
peroneus and peroneus profundus. 15, Median branch of ischiadic nerve. 16, Superficialis peroneus. 17, Lateral branch of
the ischiadic nerve.

The arteria pudenda communis (Fig. 70, No. 20) passes to the depressor coccygeus muscle, gives off a branch
to the caudal part of the kidney, crosses the ureter, provides the ischio-pubic and pubio-coccygeus, or depressor
coccygis lateralis, muscles, and on the lateral rim of the latter muscle it gives off the arteria hemorrhoidalis
intima. This artery passes to the bursa of Fabricius and to the end of the cloaca. It enters into the ischio-coccygeus
muscle, and divides into the arteria pudenda externa, and in ducks, the arteria profunda penis. These branches
supply the vas deferens, the ureter, the cloaca, the penile structure, and the muscles of these parts.

Page 250

Fig. 70.—Blood-vessels of a Cornish cock. 1, The left pulmonary artery. 2, Right pulmonary artery. 3, Left brachio-
cephalic artery. 4, Left subclavian artery. 5, Left carotid artery. 6, Right brachio-cephalic artery. 7, Posterior aorta. 8,
Posterior vena cava. 9, Left pulmonary vein. 10, Right pulmonary vein. 11, Celiac axis. 12, Anterior mesenteric artery. 13,
Ischiadic artery. 14, Crop. 15, Superior artery of the crop and vein of same name. 16, Testicular or ovarian artery. 17,
External iliac artery. 18, Intercostal nerve. 19, Median sacral artery. 20, Arteria pudenda communis. 21, Anus. 22, Vena
hypogastrica. 23, Right vena hepatica magna. 24, Left vena hepatica magna. 25, Vena iliaca interna. 26, Vena iliaca
communis. 27, Vena iliaca externa. 28, Vena coccygo-mesenterica. 29, Vena umbilicalis. 30, Vena suprarenalis. 31, Origin
of the pars renalis. 32, Lumbar veins. 33, Vena epigastrica. 34, Lumbales (arteries). 35, Anterior division of the lumbo-
sacral plexus. 36, Posterior division of the lumbo-sacral plexus. 37, Left anterior vena cava. 38, Right anterior vena cava.

The Sacralis Media.—The median coccygeal artery (Fig. 70, No. 19) forms the single extension of the sacralis
media. It gives off lateral branches between the caudal vertebræ which supply the dorsal muscles of that region and
the skin. The third pair are the largest. These are the arteriæ coccygeæ laterales, and are located on the dorsal side
of the tail, they supply the tail glands and rudder feathers, the main tail feathers, or rectrices. A small arterial twig
is given off to the papilla of each rectrix.

The Venous Trunks

The venous blood enters the lungs from the right ventricle through the two pulmonary arteries (Fig. 70, No. 1
and 2).
The two pulmonary veins (Fig. 70, No. 9 and 10) collect the arterial blood from the lungs, and empty it into the
left auricle.
There are three venæ cavæ which collect the systemic blood and empty it into the right auricle. These venæ
cavæ are two anterior (Fig. 70, No. 37 and 38) and one posterior (Fig. 70, No. 8).
Each anterior vena cava is formed by the union of a vena jugularis, a vena vertebralis, and a vena subclavicularis
(Fig. 63, No. 15).

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Fig. 71.—Veins of the liver of a fowl. 1, Vena mesenterica communis. 2, Vena portalis propria. 3, Anterior vena
mesentericus. 4, Vena portalis dexter. 5, Vena portalis sinister. 6, Posterior vena cava. 7, Celiac axis. 8, Base of the heart. 9,
The liver. 10, Hepatic veins.

The jugular vein is formed by the union of the vena cephalica anterior, and the vena cephalica posterior.
The jugular vein (Fig. 62, No. B, 3) passes along the side of the neck and lies near the trachea, the esophagus,
and the pneumogastric nerve. Near the base of the skull the two jugular veins, the right and the left, are connected
by a transverse vein. By this anastomosis part of the blood from the left jugular vein is sent into the right.
Therefore the right jugular vein is larger than the left. The jugular veins collect the blood from the tongue region,
the thyroid, the esophagus, the trachea, the crop, and other structures along its course through the cervical region.
The vertebral veins are divided into the anterior and the posterior, or the inferior and the superior. The anterior
vertebral vein is located in the cervical region and collects the blood from the brain and the inner part of the head.
The vertebral vein passes along the dorsal side of the spinal cord.

BRANCHES OF THE VENÆ CAVÆ ANTERIORES

( Venæ linguales

( Vena occipitalis lateralis ( Vena occipito-collores

( Vena ascendenes lateralis

( Venæ colli cutineæ

( Venæ esophagealeæ

( Venæ tracheales

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( Vena ( Vena subscapularis

( jugularis ( Venæ glandularum thyroidearum

( ( ( Vena occipitalis ( Sinus foraminis

( ( ( interna ( occipitalis

( ( Vena (

( ( vertebralis ( Vena vertebralis posterior ( Vena intercos

Vena cava ( ( ( Vena vertebralis anterior

anterior ( ( Vena vertebralis

( Vena vertebralis lateralis dorsalis ( Venæ intercostales

(

( Venæ coronariæ

( Vena subclavicularis

( Vena thoracica interna ( Vena intercostales

( Vena pharyngea superior

( Vena muscularis depressoris mandibularis

Vena facialis ( Vena muscularis colli anterior superioris

communis ( Vena lingualis

( Vena sublingualis et sphenoidea

Page 253

The posterior vertebral vein is located in the dorsal region, passes backward and receives the blood from the
dorsal neck region and from the intercostal veins and from the vertebral segments and adjacent regions.
The anterior and the posterior vertebral vein form one trunk, the vertebral vein, and this trunk empties into the
vena jugularis just before the subclavian and the jugular unite.
The subclavian vein collects the blood from the anterior extremities. It unites with the vena jugularis of the
same side.
The left vena cava receives the coronary veins from the heart.

Page 254

THE VEINS OF THE HEAD

Branches of the Vena Facialis Interna

The vena facialis interna (Fig. 62, No. 12) lies dorsal on the pterygoid bone and receives the vena maxillaris,
the vena ophthalmica, the vena mandibularis interna, the venæ pharyngeæ superiores, and the vena retis mirabilis
temporale.

Fig. 72.—Blood-vessels and nerves of the abdominal cavity
and hind extremity and head. 1, Vena renalis. 2, Vena
intervertebrales sacrales. 3, Posterior aorta. 4, External iliac.
6, Ischiadic nerve. 7, Ischiadic artery. 8, Arterial rete (plexus
temporalis). 9, Ophthalmic artery. 10, Palatine artery. 11,
Lingual artery. 12, Hyoid artery. 13, 14, External carotid
artery. 15, Internal maxillary artery. 16, Superior laryngeal
artery. 17, Superior esophageal artery. 18, Occipital artery.
19, Internal carotid artery.

The vena maxillaris comes out of the upper beak with the recurrent trigeminus nerve and then passes backward
between the jugular and palatine bones. It lies medio-ventrally to the eyeball and communicates at this point with
the ophthalmic vein. It is covered ventrally with the pterygoid bone. The maxillary vein collects the blood from the
gland of Harder, the upper beak, and receives blood from the vena supra-palatina and from the lower jaw bone
and the external mandibular vein. It also receives blood from the external sublingual vein, and the sublingual
gland. It follows the inner rim of the jaw bone. The maxillary vein receives an anastomosing branch from the
cutaneous facial vein, at a point near the commissure of the mouth.

Page 255

Fig. 73.—Photograph of blood-vessels and nerves of the
thorax. 1, Vena sternalis. 2, Vena thoracico-externa. 3,
External thoracic artery. 4, Coracoid bone. 5, Sternum. 6,
Shoulder-joint. 7, Humerus. 8, Clavicularis artery. 9, Sterno-
clavicularis artery. 10, Thoracico-humeralis artery. 11,
Subclavian artery. 12, Axillary artery. 13, Brachialis
profundus artery. 14, Ulnar artery. 15, Radial artery. 16,
Internal mammary artery. 17, Superior vein of the crop. 18,
Superior artery of the crop. 19, Brachial nerve plexus. 20,
Anterior division of brachial nerve plexus. 21, Posterior
division of brachial nerve plexus.

The vena ophthalmica lies close to the point where the olfactory nerve passes out of the cranial cavity. The
largest branch it receives is the recurrent ophthalmo-temporalis, which accompanies the lateral side of the optic
nerve. It collects the blood from the base of the brain, from Harder’s gland, from the eye muscles, from the inner
eye, the nose, the lacrimal gland, the skin of the frontal region, and the comb.

BRANCHES OF THE VENA JUGULARIS

( Vena maxillaris

( Vena ophthalmica

( Vena facialis ( Vena mandibularis interna

( interna ( Vena retis mirabilis temporalis

( Vena cephalica ( ( Venæ pharyngeæ superiores

( anterior or (

( facialis ( ( Vena facialis cutinea

( communis ( ( Vena temporalis

Page 256

( ( Vena facialis ( Vena auricularis

Vena jugularis ( ( externa ( Vena palpebralis

or cephalica ( ( Vena transvers

communis ( ( Vena retis m

( Vena subclavia

( Venæ vertebrales

( ( Sinus cranii et cerebri

( ( Vena carotis

( (

( ( Vena auris ( Sinus foveæ cerebelli

( ( ( Vena occipitalis ext

( Vena cephalica ( Vena jugularis prima

( posterior ( Vena occipitalis

( Vena lingualis

( Vena mandibularis externa

Vena maxillaris ( Vena sublingualis externa

( Vena supra-palatina

Vena ophthalmica ( Vena ophthalmo-temporalis, recurrent

Page 257

Vena facialis communis ( Vena cephalica externa

Vena occipitalis externa ( Vena occipitalis interna

Vena retis mirabilis temporalis ( Vena spheno-temporalis

Sinus foveæ cerebelli ( Sinus occipitalis externa

The trunk of the internal facial vein receives the blood of the internal mandibular vein. The internal
mandibular vein emerges from the alveolar canal of the inferior jaw bone and receives branches from the muscles
of mastication.
The vena retis mirabilis temporalis passes out of the eye cavity and lies between the internal facial vein and
the external facial vein, and passes around the os quadratum and the os pterygoideum. It receives veins from the
outer ear region, lacrimal gland, eyelids, and the spheno-temporalis.
The venæ pharyngeæ superiores are the veins on the dorsal surface of the pharynx. These veins form the small
plexuses which unite with the two trunks of the facial veins. This forms an anastomosis between the left and the
right facial veins.

Branches of the External Facial Vein

The vena facialis externa (Fig. 62, No. B, 9) lies behind the quadrate bone and is partly covered ventrally by the
inner extension of the lower jaw bone. It collects the blood principally from the upper region of the cranium and
the face, including the comb.
The vena facialis cutinea receives branches from the muscles in the region of the jaw, the lower jaw bone, the
muscles of the eyelids, the frontal region, and the anastomotic branches from the vena maxillaris.
The vena temporalis is made up of veins from the skin of the temporal region, the masseter and the tongue
muscles, and from the sides of the upper throat region.
The vena palpebralis is made up from veins from the three eyelids and the temporal region near the eye. Its
trunk passes laterally over the temporo-mandibularis ligament. The vena palpebralis collects blood from the

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lacrimal gland, the eyelids, and the outer ear region.
The following veins empty into the trunk of the vena facialis communis: venæ pharyngis superiores, vena
muscularis depressoris mandibulæ, vena muscularis colli anterior superioris, vena lingualis et hyoidea. The right
terminal branches of the vena lingualis empty into the vena cephalica posterior.
The venæ pharyngis superiores and vena lingualis et hyoidea collect blood from the muscles of the tongue and
posterior tongue region.
The vena lingualis et hyoidea (Fig. 62, No. B, 7) collects the blood from the muscles of the tongue region, the
lower tongue glands, and the upper throat region.
Between the two trunks of the vena facialis communis and anterior to the entrance of the vena cephalica
posterior there is an anastomosis, the vena transversus (Fig. 62, No. B, 5). Through this anastomosis which lies
crosswise the two jugular veins are influenced in different ways. At this point both jugular veins are of the same
size. The anastomotic branch lies crosswise. Through this anastomosis the right receives some blood from the left
head region indicating that the blood flows from left to right. This, as stated before, makes the left jugular vein the
smaller.

Branches of the Vena Cephalica Posterior

The left vena cephalica posterior (Fig. 62, No. B, 8) communicates with the transverse vein (Fig. 62, No. B, 5).
The left receives the smaller veins of the skin region, the esophagus, and the trachea. These vessels communicate
with their fellow of the opposite side and with the vertebral vein of the same side, which causes a gradual
reduction of the size of the jugular vein.

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BRANCHES OF THE VENA OCCIPITALIS EXTERNUS

( ( Venæ choroideæ

( Sinus ( Venæ cutaneæ et frontales

( longitudinalis ( Venæ nasales

Vena ( ( Venæ ophthalmiæ

occipitalis (

externus ( ( ( Sinus occipitalis

( Sinus ( Sinus ( Sinus temporo-sphenoideus

( semicircularis ( transversus ( Venæ cerebellares

( ( ( Sinus petrosus sphenoideus

Sinus petrosus sphenoideus ( Retis mirabile temporalis

Sinus temporo-sphenoideus ( Sinus annularis venosus basilaris

Sinus foraminus occipitalis ( Venæ medullares

( Venæ cerebrales

Sinus ( Vena cerebralis basilaris ( Sinus venosus annularis anterior

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venosus (

annularis (

basilaris ( Vena ophthalmica

( Vena medullaris mediana longitudinalis

The vena cephalica posterior (Fig. 62, No. B, 8) is formed from the veins of the sinuses of the cranium, the
brain, the vena auris, the vena jugularis prima, the vena carotis, and the vena occipitalis. It collects most of the
blood from the cranium and the posterior part of the head and from the tongue.

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THE VENOUS SINUSES OF THE HEAD

The sinus longitudinalis (Fig. 62, A, 10) extends from the dorsal median line of the internal occipital
protuberance to the olfactory nerve. It collects the blood from the choroidea of the brain and from the skin of the
frontal region. It receives laterally the veins of the nose, the vena ophthalmica, and the sinus transversus.
The sinus occipitalis (Fig. 62, No. A, 4) forms the continuation of the transverse sinus. It is located in the
posterior cerebral cavity, and is wing-shaped, extending both to the right and to the left.
The sinus foraminis occipitalis a continuation of the sinus occipitalis, lies transversely on the ventral side of
the cranial cavity and receives the veins from the medulla oblongata. One branch passes through the os occipitalis
basilare, and then extends sidewise to the foramen magnum and anastomoses with the vena occipitalis.
The sinus transversus (Fig. 62, No. A, 6) extends in a pair from the internal occipital protuberance between the
cerebrum, cerebellum, and the corpus quadrigeminum. It receives vessels from the upper surface of the
cerebellum. The sinus has three branches, all of which empty into the sinus semicircularis.
The sinus semicircularis extends along the dorsal petrosal rim, anterior to the inner ear, and from this point
backward. Near the foramen magnum it passes through the os occipitale and empties into the external occipital
vein.
The vena occipitalis externus extends near the foramen magnum, surrounds the basis occipitalis, and receives
the semicircular sinus and through the semicircular sinus the blood from the sinus transversus.
The sinus petrosus sphenoideus, passing in company with the occipital sinus, extends from the transverse sinus
to the cavity near which the trigeminus lies. The sinus dividing into two branches, one of these extends to the
hypophysis and unites with the basal veins of the brain; the other passes with the rete out of the cranial cavity
along with a branch of the trigeminus, and communicates with the rete mirabile temporale.
The sinus temporo-sphenoideus (Fig. 62, No. A, 5) extends forward and outward from the transverse sinus,
and, between the corpus quadrigeminum and the cerebrum, unites with the sinus venosus annularis basilaris.
The sinus venosus annularis basilaris lies in the region of the optic nerve and surrounds the hypophysis,
forming a complete circle. It receives small vessels from the cerebrum, the corpora quadrigemina, and anteriorly
the longitudinal basilar vein or vena basilaris media, of the cerebrum, which comes out of the anterior annular
venous sinus. The anterior annular venous sinus surrounds the base of the olfactory nerves. It communicates with
the sinus petrosus sphenoideus, which emerges from behind the optic lobe, the sinus temporo-sphenoideus, which
emerges from in front of the optic lobe, and posteriorly the median longitudinal vein of the medulla oblongata or
vena basilaris. Laterally and anterior to the optic lobe it receives the vena basilaris lateralis, and also a branch of
the vena ophthalmica.
The blood received by the sinus annularis basilaris comes from the brain cavity through three pairs of veins, as
follows: first, the two ophthalmic veins which pass through the posterior orbital wall between the olfactory and the
optic nerve; second, two other branches of the ophthalmica which pass with the optic nerve; third, two veins which
pass through a foramen by the side of the sella turcica to the hypophysis together with the carotis cerebralis, and
then leave the cerebral cavity ventrally, at which point they are called the venæ carotes. These last accompany the
cerebral artery backward, and pass through a foramen in the base of the cranium. Each one then passes through the
cranial wall close to the external auditory canal, and empties into another vein in the posterior region of the head.
The sinus fovæ hemispherii cerebelli lies in the hollow between the os petrosum and the semicircular canals. It
receives blood from the external occipital sinus and from the cerebellum, and empties into the vena auris interna.

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VEINS OF THE BRAIN CAVITY

The vena auris interna passes through a bony canal along the outer rim of the posterior semicircular canal and
then along the external semicircular canal. It receives vessels from the labyrinth, and extends along the posterior
rim of the tympanum to the outer ear canal.
The vena occipitalis interna, extending from the sinus foraminis occipitalis, passes through the side of the atlas
and divides near the condyle into two branches. One of these branches the internal occipital, forms the root of the
vena vertebralis, and the other empties into the vena occipitalis externa.
Near the outer and upper part of the condyle it forms two large veins and collects the blood from the vena
occipitalis media. These veins collect the blood from the rectus capitis anticus, and communicate with the vena
cephalica anterior.
The vena occipitalis externa, sometimes called the vena occipitalis collateralis, extends from the vena auris,
and receives vessels from the neck region. It receives on the side of the occipitoatloid joint the vena occipitalis
interna. The vena occipitalis externa forms a junction with the vena vertebralis emptying into the transverse vein.

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THE VEINS OF THE NECK

Branches of the Vena Jugularis

The trunks of the vena jugularis or vena cephalica communis pass subcutaneously on both sides near the trachea
and the esophagus. Near the height of the thyroid gland they almost touch the carotid artery. They then cross,
dorsalward, the trunk of the subclavian artery, and in their course receive the vertebral vein and unite with the
subclavian vein toward the side of the vena brachiocephalica. The union on the right side lies to the right of the
anterior aorta, and the union on the left side lies to the left of the pulmonary artery.
The jugular vein (Fig. 18, No. 4) receives in its course the following veins:
The venæ linguales (Fig. 62, No. B, 7), which at times empty into the vena cephalica posterior.
The vena occipito-collares, which arises on the ventral side from the muscles of the neck and the vertebræ;
empties into the vena occipitalis lateralis and also communicates with the vena jugularis by anastomoses.
The venæ ascendentes laterales, which collect blood from the lateral sides of the neck.
The venæ colli cutineæ, which enter the jugular vein laterally. The upper branches are directed crosswise, and
are shorter than the lower ones. The lower branches are located near the thorax, are directed upward, and
anastomose by fine terminal twigs. Plexuses are frequently formed in the inner side of the skin of the neck.

BRANCHES OF THE VENA SUBCLAVIA

( Vena profunda ulnaris

( Vena brachialis ( Vena profunda radialis

( Truncus venæ ( ( Vena profunda humeri

( axillaris (

( ( Vena basilica or cutinea ulnaris

(

( ( Vena cutinea abdomino-pectoralis

Truncus venæ ( Vena pectoris ( Vena infrascapularis anterior

subclaviæ ( externa ( Vena thoracica externa

( Vena coracoidea

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( Vena sternalis

The venæ esophageæ are numerous smaller veins formed in closely woven plexuses in the region of the
esophagus along the neck. Some pass upward and some downward.
The venæ tracheales are located on the supero-lateral side of the trachea and along the edge of the lateral
tracheal muscle. They have numerous anastomoses transversely with the longitudinal vein of the cervical region,
anteriorly with the vena lingualis, and on the left side with the left jugular vein.
The vena subscapularis passes along the median line of the scapula to the side of the jugular vein, and
anastomoses with the vertebral vein.
The venæ glandularum thyroidearum are several small, short veins coming from the thyroid gland.
The vena vertebralis, originating near the atlas, is a continuation of the internal occipital vein. The internal
occipital vein receives the bulk of the blood from the brain and communicates with the lateral veins of the cervical
region and collects blood from the cervical vertebra. The vertebral vein accompanies the vertebral artery and the
deep sympathetic nerve trunk in the vertebral canal. The vein either leaves this canal with the vertebral artery at a
point near the last two vertebral nerve trunks of the brachial plexus, or it leaves the canal one vertebra in front of
the vertebral artery.

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THE VEINS OF THE DORSAL REGION

The vena vertebralis lateralis dorsalis collects blood from the cervical vertebræ, from the dorsal vertebræ, and
from the intercostal region.
The blood from the neural canal, including the spinal cord, is collected in one long vein extending from the head
to the tail on the upper side of the cord. This vein has sinus-like expansions. Between each two vertebræ it
anastomoses with the vertebral vein on each side. In the lumbo-sacral region these anastomotic branches empty
into the hypogastric veins.
The vena intercostalis is formed in the costal region and anastomoses with the vein extending longitudinally
between the capitulum and the tuberculum of the rib.
The vena vertebralis posterior at the height of the first and the second dorsal vertebræ, empties into the main
trunk of the vertebral vein. Its lower roots come out near the side of the kidney, and unite, forming a large
ascending trunk uniting with the vena vertebralis anterior forming one large trunk, which extends into the chest
cavity.
The posterior vertebral vein also receives a large vein from the skin of the outer tarsal region and a few vessels
from the muscles of the outer abdominal and the outer costal region, from the skin, from the pectoralis muscles,
and from the shoulder region.

Page 266

VEINS OF THE THORAX

Branches of the Vena Subclavia

The vena thoracica externa (Fig. 73, No. 2) is made up of veins mainly from the pectoral group of muscles.
The posterior branch anastomoses with the vena cutinea. Its anterior branch is made up mainly of branches from
the furcular region. It empties into the vena pectoralis externa and the vena pectoralis externa empties into the vena
subclavia.
The vena coracoidea comes out of the region of the shoulder-joint, passes downward along the inner surface of
the coracoid, and receives small branches from the walls of the arteria brachia cephalica and from the pericardium.
The vena sternalis (Fig. 73, No. 1) is made up of two branches. The outer branch comes from the muscles of
the subclavian region passes over the cristi sterni, medially, to the sterno-coracoid joint and into the breast cavity,
where it receives the inner branch, which drains the inner surface of the breast-bone.
The vena thoracica interna empties into the vena cava anterior. It extends from the abdominal muscles where it
communicates with the epigastric vein. It then passes on the inner side of the thoracic cavity close to the breast-
bone and receives many intercostal veins.
The vena cava sinistra receives first, the vena proventricularis communis, which collects the blood from the
walls of the proventriculus, and second, the vena coronaria cardis magna. This latter vein originates close to the
apex of the heart and collects blood principally from the walls of the left ventricle. It connects in the left sulcus
transversus with the vena cardis superior and ends at the base of the left upper vena cava. Its exit is not guarded by
a valve. The veins of the right ventricle are partly on the surface. They collect blood along the sulcus transversus
dexter and enter directly into the right ventricle. The veins of the front part of the heart are small. They collect
behind the sulcus coronalis and end either directly into the right auricle or into the vena cardis magna.

Page 267

VEINS OF THE FORE LIMB

The vena radialis profunda accompanies the radial artery on the dorsal anterior rim of the index-finger and
passes, on the dorsal side, over the carpal region. It passes through the interosseous ligament between the ulna and
the radius, and reaches the ventral surface of the arm. At this point it passes upward and anastomoses with the vena
ulnaris. It collects the blood from the skin of the anterior wing region and the flexor muscles of the anterior arm. It
empties into the vena brachialis.
The vena humeri profunda (Fig. 68, No. 1) emerges at the height of the elbow, and collects blood from the
skin of the dorsal surface of the wing. It also receives veins from the muscles of the posterior side of the upper
arm. It passes subcutaneously and dorsally over the dorsal portion of the humerus in company with the external
radial muscle and passes with it around the external part of the humerus between the long and short heads of the
triceps. It takes a diagonal course to the shoulder cavity and at that point empties into the brachial trunk.
The profundus ulnaris originates at the volar surface of the hand, proceeds in company with the ulnar artery,
and sends on the base of the hand small anastomotic veins to the vena cutanea ulnaris or basilica. It passes along
the anterior arm and between the flexor carpi ulnaris and the pronator profundus muscle to the elbow-joint. On the
median surface of the biceps it passes upward and anastomoses with the radial vein. The ulnar vein, in the region
of the elbow-joint, receives a large lateral branch which extends around the end tendon of the biceps and
anastomoses above with the vena basilica.
The vena basilica or cutanea ulnaris is a long vein which originates from the subcutaneous dorsal surface of the
index-finger. Near the base of the hand it receives an anastomosing branch from the vena radialis and the vena
ulnaris, and then passes upward along the posterior rim of the ulna. It receives numerous branches from the roots
of the flight feathers. It crosses below the elbow-joint and reaches the volar surface of the arm. It receives a large
branch from the ulnar vein, and then, passing in a diagonal and median direction to the triceps, extends to the
shoulder cavity where it empties into the axillary vein.
The outer breast veins unite forming a trunk which crosses ventrally to the subclavian artery, and empties into
the subclavian vein.
The vena cutanea abdomino-pectoralis collects the blood from a large skin area of the abdomen, the upper thigh,
the breast, and the intercostal region. In the skin of the abdomen it forms a network.

BRANCHES OF THE ILIACS

( Vena metatarsalis ( Vena metatarsalis

( Vena ( interna or magna ( plantaris profunda

( tibialis ( Vena tibialis antica

( postica ( Vena metatarsalis ( Venæ metatarsales

( ( externa

(

Page 268

( Vena ( Vena metatarsalis dorsalis profunda

( Vena ( tibialis ( Vena metatarsalis dorsalis interna

( poplitealis ( antica ( Vena peronealis

( ( Vena cutanea cruralis

( ( Venæ surales

Vena (

iliaca ( ( Vena cutanea abdominalis femoralis

externa ( Vena ( Vena femoralis interna profunda

( cruralis ( Vena femoralis anterior

( ( Vena epigastrica

The main trunk passes in the median abdominal line forward and then upward, along the outer edge of the
pectoralis major, over the first sternal rib; receives blood from the infrascapular vein, and empties into the
pectoralis externa.
The vena brachialis is located in the middle of the humerus and the triceps muscle. It is formed by the vena
ulnaris, and the vena radialis. It passes with the median nerve and the brachial artery over the inner surface of the
humeral joint. Posterior to the humeral head it receives the vena profunda humeri. At the shoulder cavity it
receives the vena cutanea ulnaris or vena basilica.
The trunk of the axillary vein is very short and is formed by the veins of the shoulder and the wing. The deeper
wing veins accompany the large arterial and the nerve trunks.

BRANCHES OF THE VENA ILIACA INTERNA

( Vena intervertebralis lumbalis

( Pars truncalis ( Vena renalis magna

( (

Page 269

( ( ( Vena hypogastrica cauda

( ( Vena renalis ( Vena hypogastrica caudalis d

( ( ( Vena portalis

( ( Vena coccygea ( Vena cutanea et pudenda

Vena iliaca ( ( Vena coccygea

interna or ( ( Vena cutanea pubica

vena hypogastrica ( Pars caudalis ( Vena cutanea caudalis

( ( Vena pudenda ( Vena spermatica

( ( Vena caudalis muscularis

( ( Venæ sacrales

( ( Venæ intervertebrales sacralis ( Venæ renales

( ( Venæ renales

( Pars renalis ( Vena ischiadica

( Vena obturatoria

( Vena suprarenalis externa ( Azygos sacralis

Page 270

THE POSTERIOR VENA CAVA

The posterior vena cava (Fig. 63, No. 18; Fig. 70, No. 8) has its origin in the posterior half of the body of the
bird, somewhat to the right of the posterior aorta, near the anterior lobe of the kidney, by the union of the right and
the left vena iliaca communis. It receives the blood from all of the posterior half of the body including the posterior
limbs, of the visceral organs, of the abdominal and the pelvic cavity. The posterior vena cava passes dorsally
through the right lobe of the liver and through the diaphragm and ends in a short, broad trunk on the posterior
dorsal side of the right auricle of the heart. Its opening into the heart is guarded by two half-moon shaped valves.
The basal part of the trunk reaches from the right auricle of the heart to the upper anterior rim of the liver where it
receives three large trunks, first, the right and second, the left vena portalis hepatica magna, and third, smaller
vessels from the liver substance.

Page 271

THE VEINS OF THE POSTERIOR EXTREMITY

In the skin region on the inner sides of the toes near their bases the small veins collect into five metatarsal veins.
The largest vein collects the blood from the first, the second, and the third toe, passes up the tarsus and is called the
vena metatarsalis interna, or vena magna (Fig. 65, No. 7). It is located just beneath the skin on the inner surface of
the metatarsal bone. It passes in a circle, around the condyle of the tibia and becomes the vena tibialis postica
(Fig. 65, No. 3 and 8). The vena tibialis postica passes under the tendon Achillis and the tendon of the flexor
digitorum brevis, lies subcutaneously upon the latter, and reaching the knee-joint crosses over the upper surface of
the ischiadic nerve and becomes the vena poplitealis, at which point it receives the vena tibialis antica.

BRANCHES OF THE VENA CAVA POSTERIOR

( Vena ovariana

( Venæ testiculæ

( Vena proventricularis communis

( Vena suprarenalis revehentis

( Vena portalis magna sinistra

( Vena portalis magna dextra

( Venæ innominatæ

( Venæ hepaticæ

Vena cava ( Vena cardis coronaria magna

posterior ( Vena proventricularis inferior

( ( Vena iliaca interna ( Vena hypogastrica

( ( Vena iliaca externa ( Vena renalis

( ( Vena suprarenalis externa

( Vena iliaca ( Vena ischiadica

Page 272

( communis ( Vena renalis

( ( Vena intervertebralis lumbalis

( ( Vena renalis magna

( Vena mesenterica communis ( Vena coccygo-mesenterica

Vena ( ( Vena mesenterica anterior

portalis ( Vena pancreatico-duodenalis

dextra ( ( Vena proventricularis

( Vena proventricularis lienalis ( Vena splenica

Vena coccygo-mesenterica ( Vena hemorrhoidalis

On the dorsal side of the metatarsus are two veins. The vena metatarsalis dorsalis profunda (Fig. 65, No. 11),
which extends under the tendon of the extensors of the toes, along with the artery and the nerve. It collects the
blood from the third and the fourth toe and in the middle of the metatarsus receives the vena metatarsalis dorsalis
interna (Fig. 65, No. 4), which connects the vena metatarsalis dorsalis profunda and the vena magna. The two
dorsal veins anastomose with the vena magna, at the intertarsal joint. They pass transversely under the ligament
and form the main trunk of the vena tibialis antica which lies close to the anterior surface of the tibia. Near this
point there is formed a plexus of veins which again form a trunk and communicates with the vena peronealis and
enters between the tibia and fibula with the tibialis antica. It extends along the flexure of the knee and the posterior
part of the lower thigh.
The vena metatarsalis externa passes subcutaneously on the outside of the fourth toe and the metatarsus, and
above the intertarsal point joins the tibialis postica.
The vena metatarsalis plantaris profunda (Fig. 65, No. 5) lies on the ventral side of the foot and forms several
anastomosing arches with the other veins of the toes. Below the intertarsal joint it enters the vena metatarsalis
magna (Fig. 65, No. 9).
The vena cutanea cruralis (Fig. 69, No. 7) originates at the height of the tarsal region and passes
subcutaneously on the outer posterior surface of the lower thigh region to the vena poplitealis.
The venæ surales or inferior muscular branches of the vena poplitealis consist of many veins. One branch
comes from the region of the shank and from the gastrocnemius muscle; another as a main branch from the

Page 273

posterior surface of the lower thigh; and a third from the outer surface of the muscles and skin of the upper thigh.
The three branches together with the anterior and posterior tibial (Fig. 69, No. 2) unite at the flexure of the knee
forming the vena poplitealis (Fig. 69, No. 1).
In the region of the upper thigh, between the knee and the abdominal cavity, the following four veins form the
vena cruralis: (Fig. 66, No. 6; Fig. 69, No. 5). First, the vena cutanea abdominalis femoralis (Fig. 69, No. 6)
which comes out of the side of the abdominal wall, draining the skin of the inner surface of the upper portion of
the thigh, the adductor muscles, and the region of the abdominal and the breast border. It crosses the ischiadic
artery in a diagonal direction, and enters the vena cruralis in the middle of the crural region.
Second, the vena femoralis interna profunda (Fig. 69, No. 3) forms a communication between the end of the
suralis near the knee. It lies on the median portion of the flexor cruris internus muscle.
Third, the vena femoralis anterior (Fig. 69, No. 4) is formed from branches from the sartorius and adjacent
structures, and anteriorly empties into the crural vein near where the latter enters the abdominal cavity.
Fourth, the vena epigastrica (Fig. 70, No. 33) is formed by branches from the abdominal wall and branches
from the walls of the abdominal air-sacs. It passes along the median surface of the os pubis and ends into the vena
cruralis near the spine of the ilio-pubica or at a point where these join with the vena hypogastrica.

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VEINS OF THE CAUDAL REGION AND OF THE PELVIC CAVITY

The vena iliaca interna or the vena hypogastrica (Fig. 70, No. 22) collects most of the blood from the tail. The
vena iliaca interna collects most of the blood from the pelvic cavity, and the adjacent intestines. It unites with the
vena iliaca externa (Fig. 70, No. 27) and receives the vena renalis magna and forms the trunk of the vena iliaca
communis (Fig. 70, No. 26).
The vena coccygea originates between the coccygeal vertebræ, and collects the blood from the region of the tail,
including the tail feathers, the tail muscles, the tail gland, and the skin of the region. These small collecting vessels
form a trunk on each side of the coccyx. The right and the left pass laterally, each one taking up a vena cutanea et
pudenda, and frequently anastomosing with the vessels on the other side. These often unite into one vessel. Both
trunks are connected by a transverse, or anastomotic, vessel. At this anastomosis there empty into it the vena
coccygea mesenterica and the vena portalis. There also communicate at this point the right and the left
hypogastrica caudalis. In its course it is partly imbedded in the kidney and passes anteriorly to the vena iliaca
communis. This circle is called the arcus hypogastricus. Thus the veins of the abdominal cavity have many
anastomoses forming many arcs, making possible two outlets for the blood.
The azygos sacralis empties into the arcus at about its middle. From here it extends forward to the inside and
under the kidney and empties into the vena suprarenalis externa.
The vena cutanea pubica originates on the lower portion of the abdomen, collects the blood from the muscles
of the distal part of the ischium, and enters the pelvic cavity between the ischium and the ilium. It joins with the
vena cutanea caudalis.
The vena cutanea caudalis originates from branches which drain the skin and other parts of the ventral
coccygeal region. The vena cutanea pubica also communicates with the vena caudalis muscularis and with the
vena pudenda, thus forming the caudal trunk of the vena hypogastrica.
The vena pudenda originates in the walls of the cloaca in the region of the generative organs.
A small vena spermatica accompanies the lower end of the vas deferens and the ureter, and empties medially
into the vena pudenda.
The pars renalis of the vena hypogastrica extends from the middle of the arcus to the union of the vena
hypogastrica and the vena cruralis.
The vena hypogastrica communicates with the pars renalis. The vessels that empty into the pars renalis are as
follows:
The venæ sacrales collect blood from the dorsal wall of the abdominal cavity and enter the pelvis through the
foramen sacralis. They pass between the pelvic wall and kidney, and at times pass through the kidney tissue. They
empty into the pars renalis of the hypogastric arch.
The venæ intervertebrales sacrales (Fig. 72, No. 2) originate in the region of the roots of the plexus of sacral
nerves and pass through the kidney substance or on the dorsal surface and empty into the pars renalis.
The venæ renales (Fig. 72, No. 1) are very numerous and originate in the kidney substance, forming two main
and several minor branches, which pass posteriorly, and empty partly into the vena hypogastrica, partly into the
vena renalis magna, and also into the vena intervertebralis; other branches empty into the trunk of the iliaca
communis.
The vena suprarenalis externa (Fig. 70, No. 30) is located near the anterior rim of the kidney and is connected
with the vena hypogastrica. It also receives on the medial side, short branches which come out of the upper kidney
surface and sacral vertebræ.
The vena ischiatica originates by the union of several venous branches which come from the muscles of the
pelvis and upper thigh region. The ischiatic vein enters the pelvic cavity along with the ischiatic nerve and artery,
and communicates with the vena hypogastrica at about the level of the anterior lobe of the kidney. It is always
smaller than the vena cruralis.
The vena obturatoria originates mainly from vessels from the obturator muscles. It enters the pelvic cavity
through the obturator foramen. Another branch is sometimes found which comes out of the inner surface of the
peritoneum which covers the obturator muscles and the walls of the abdominal air-sacs and empties between the
vena ischiatica and the vena vertebralis into the vena hypogastrica.

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VEINS OF THE TRUNCUS VENA ILIACA COMMUNIS

The vena intervertebralis lumbalis, which comes out of the lumbar region, the spinal canal, the lumbo-sacral
nerve plexus, and several small venous branches from the lobes of the kidney. It passes dorsalward through the
kidney and empties into the iliac vein. There are also communications with the vena intervertebralis thoracica.
The vena renalis magna (Fig. 64, No. 47) forms the main descending vein to the middle and posterior lobes of
the kidney. It lies ventrally and mesially on the middle lobe and partly on the inner part of the posterior lobe. It
sometimes has on each side two main trunks. The vein receives some small vessels out of the anterior kidney lobe,
also other small veins from that part of the peritoneum which covers the kidney, from the rectum and finally small
veins from the ureter.

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VISCERAL VEINS OF THE POSTERIOR VENA CAVA

The venæ testiculæ, or the vena ovariana drain the blood from the testicles of the male and ovary of the female.
The size of these veins change with the enlargement of the testes or of the ovary during reproductive activity.
The venæ suprarenales revehentes are short, thick trunks coming from the adrenal glands. The left empties
into the left side of the posterior vena cava and the right into the right dorsal side. These receive veins from the
testicles in the male and from the ovary in the female.
The vena proventricularis inferior drains the stomach wall. One branch of this vein enters the left side of the
posterior vena cava; the other enters the vena proventricularis communis, which in turn empties into the trunk of
the anterior vena cava sinistra.
The venæ hepaticæ consist of one large and several small veins from each lobe of the liver, and empty into the
posterior vena cava.
Some small vessels come from the pericardium and the peritoneal covering of the liver, and pass in the
mediastinum to the trunk of the posterior vena cava.
In the region of the vena portalis:
The liver receives almost all the blood from the stomach, the intestines, the pancreatic gland, the spleen, partly
from the liver itself, and partly from the abdominal air-sacs. This blood enters into the liver through the vena
portalis dextra, the vena portalis sinistra, and the vena portalis propria.
In both lobes of the liver these veins divide into numerous small branches and collect again into two large short
trunks, the vena hepatica magna dextra (Fig. 70, No. 23), coming out of the right lobe of the liver and the vena
hepatica magna sinistra (Fig. 70, No. 24) coming out of the left lobe. These two vessels empty inferiorly into the
posterior vena cava.
The vena portalis dextra receives the blood from the vena mesenterica communis.
The vena mesenterica communis (Fig. 64, No. 36) receives the blood from the vena coccygo-mesenterica (Fig.
70, No. 28) which comes from the arcus hypogastricus and receives the vena hemorrhoidalis (Fig. 64, No. 37).
This drains the cloaca and the bursa of Fabricius, and it also receives veins from the rectum and from the base of
the cæca.
The vena mesenterica anterior (Fig. 71, No. 3) accompanies the anterior mesenteric artery, and collects the
blood from numerous vessels from the small intestine.
The vena pancreatico-duodenalis (Fig. 64, No. 38) comes out of the duodenum and the pancreas, along the
right side of the stomach and along both cæca.
The vena proventriculo-lienalis (Fig. 64, No. 39) comes out of the dorsal side of the proventriculus on the left
side of the gizzard, passes along the hilus of the spleen, and takes up several splenic veins.
The vena portalis dextra (Fig. 64, No. 40; Fig. 71, No. 4) receives a vein near the base of the gall-bladder. This
branch enters the right lobe of the liver and unites with the vena portalis sinistra.
The vena portalis sinistra (Fig. 71, No. 5) enters the left lobe of the liver and there forms a sinus. It receives
vessels which come from the muscles of the gizzard, the inferior vena proventricularis, and from the proventricular
wall.
The vena portalis propria receives small veins which come out of the walls of the abdominal air-sacs and from
the fat of the abdominal walls.
The vena umbilicalis originates in the umbilical region and empties into the vena hepatica magna sinistra at a
point where it comes out of the liver (Fig. 70, No. 29). This is the remains of an embryonal vein which collected
all the blood of the yolk sac, passed on the left side of the large intestine to the body, took up the vena mesenterica
and ended as the vena umphalo-mesenterica.

The Lymphatic System

The peculiarity of the lymph vessels is that they are associated with organs in which lymph cells are formed.

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The lymphatic system consists of the lymph vessels and the cell-forming organs. In some instances the cell-
producing organs are lymph follicles and in others lymph glands. For the most part the glands are replaced by
plexuses which in many places surround the blood-vessels.
The lymph of birds is similar to that of mammals. The larger lymph vessels are similar to the veins, although the
walls are always thinner. Its tunica intima is rich in elastic fibers and has a layer of endothelial cells on the inner
side. The tunica media is formed of rings of smooth muscle fibers. The adventitia is composed of loose connective
tissue.
The lymph vessels frequently form plexuses. The large lymph trunks follow the course of the larger blood-
vessels, and frequently surround the arteries. All the lymph vessels of the body, exclusive of the lymph of the
caudal region, form into a large trunk which originates on both sides of the celiaca communis and passes upward
along the side of the abdominal aorta, reaching a point anterior to the celiaca. By receiving many vessels in this
region it forms a plexus around the aorta, and finally divides into two vessels, the right and the left, ducti thoracici.
The lymph vessels of the left side of the head, the neck, and the lung, and the left wing, and also lymph vessels
of the proventriculus and the throat enter into the left ductus thoracicus. They accompany the jugular vein and are
closely associated with the thyroid gland.
The right thoracic duct receives the lymph veins from the right cervical lymph vein, and the right side of the
head, the neck, the lung, and from the right wing.
After the right cervical lymph vein has passed through the right thyroid gland, it divides into two branches, one
branch emptying into the right thoracic duct and the other into the vena cava dextra.
The lymph vessels of the liver, the stomach, the pancreas, and the duodenum enter near the root of the arteria
celiaca into the large lymph trunk. The lymph vessels of the remainder of the intestines, of the kidney, and of the
generative organs empty farther caudally.
The lymph vessels of the intestines take up the emulsified fat. This emulsion in birds is colorless. The vessels
pass upward along the mesenteric arteries. There are no mesenteric glands. These vessels form a plexus around the
arteria celiaca. The lymph vessels of the posterior extremities accompany the artery, especially the anterior iliaca
externa, and empty into the thoracic duct at the point of the anterior iliaco-communis.
The lymph vessels in birds are numerous. The lymph glands are few. They are only visibly found in the anterior
breast and the neck region, and sometimes in the wings. Lymph follicles are numerous in the intestines.
The thin walls of the lacteals, of the lymph vessels, and of the thoracic duct are made up of two tunics, the inner
being the thinner and weaker.
The lymphatics of the foot unite to form the vessels along the sides of each toe. In palmipedes there are
anastomosing branches which pass from the lateral vessels of one toe to those of the adjoining toe, forming arches
in the uniting web of the foot. These branches form a small plexus at the anterior part of the digito-metatarsal joint,
from which pass three or four lymph vessels. The anterior and internal branches accompany and form a network
around the blood-vessels. The posterior and external branches receive the lymphatic vessels from the sole of the
foot. They then ascend along the metatarsus and form, at its proximal articulation, a close network from which
vessels pass along the tibial region, forming a plexus around it as far as the middle of the leg. From this there
arises two branches. The smaller passes along the anterior part of the depression between the tibia and the fibula,
as far as the knee-joint, where it joins the other branch, which accompanies the blood-vessel. The trunk formed by
the union of these two vessels accompanies the femoral vessels. Forming plexuses in its course, it receives
tributary vessels from the adjacent muscles. The iliac trunk accompanies the femoral vein into the abdominal
cavity, entering just in front of the anterior end of the pubis. At this point it receives branches from the lateral parts
of the pelvis and then separates into two branches. The posterior vessel receives some lymph from the anterior
lobes of the kidney, and from the ovary, or testis, and communicates anteriorly with a branch formed by the lymph
vessels adjacent to the anterior mesenteric artery, and posteriorly with a large vesicular plexus surrounding the
aorta and its branches. This plexus receives the lymph from the renal plexus and from those accompanying the
arteria media.
There are two sacral or pelvic vesicles which are situated at the angle between the tail and the thigh in the
posterior part of the abdominal cavity. Each vesicle is a trifle more than a half inch long and a quarter inch wide,
and is shaped somewhat like a kidney bean. They have muscular coats with striated fibers. These sacs are called
“lymph hearts.”
The anterior division of the femoral lymphatic trunk accompanies the aorta, on which it forms a plexus with the
branches of the opposite side, and with the intestinal lymph vessels. These vessels commence from a continuous

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plexiform network located between the mucous and the muscular coat of the intestine. They are larger at this point
than where they leave the intestine to pass through the mesentery. They accompany the trunk of the anterior
mesenteric artery and form a plexus around it.
Before reaching the region of the aorta, the intestinal lymphatic vessels communicate with the posterior division
of the femoral trunk and with the lymph vessels of the ovary or of the testis. After passing to the region of the aorta
they receive vessels from the pancreas and the duodenum, and terminate around the celiac axis with the lymphatics
of the liver, the proventriculus, the gizzard, and the spleen, forming a rather voluminous plexus (Lauth).
The aortic plexus represents the receptaculum chyli and gives origin to two thoracic ducts, mentioned above,
which passing on each side of the bodies of the vertebræ, pass one right and one left, over the lungs, from which
they receive lymph vessels, and terminate after receiving the lymph vessels of the wing, into the jugular vein of
their respective sides. The left thoracic duct, before emptying into the vein, receives the trunk of the lymphatics of
the left side of the neck, and the right duct that of the right side of the neck, each tributary collecting lymph from
all the structures of its side.
The lymphatics of the wing follow the course of the brachial artery, forming a plexus around it. These vessels
are well developed in the elbow region. The principal trunk, following the humerus, receives collateral branches in
its upper third. This vessel, when nearing the chest, receives two or three large lymph vessels from the pectoral
muscles, and a branch which accompanies the brachial plexus.
The lymph vessels of the head accompany the branches of the jugular vein, collecting the lymph from the
structures of the head and the neck.
The lymphatic vessels communicate at the anterior and posterior oblique anastomosing vessels. At the lower
part of the neck each trunk receives a vessel, which accompanies the carotid arteries. Further on they are provided
with a lymph gland which rests on the jugular vein.

The Blood and Its Functions

The special function of the blood is to nourish all the tissues of the body, and in this way to aid growth and
repair. It furnishes material for the purpose of the elaboration of body secretions; it supplies the organism with
oxygen; and it carries away carbon dioxid and other effete material. Blood is constantly in circulation.
Blood is red, opaque, and is, in the fowl, quite viscid. The exact tint of the blood depends on whether it is drawn
from an artery or from a vein. Blood from a vein has a purplish tinge while that from an artery is a bright scarlet.
The color of blood is largely due to pigment in the erythrocyte, called hemoglobin.
The reaction of the blood is alkaline, due to the phosphate and the bicarbonate of soda. The alkalinity of the
blood is reduced by work. This is due to the formation of sarcolactic acid in the muscle. The odor of blood is due
to volatile fatty acids. Each kind of fowl has its own peculiar odor. The taste of the blood is saltish, due to a small
amount of sodium chlorid it contains.
The blood consists of the following substances:
First, the unorganized part, or fluid, the liquor sanguinis or plasma. It contains in solution proteids, extractives,
mineral matter, and gases. The gases are held in loose chemical union.
The liquor sanguinis constitutes fully 66 per cent. of the volume of the blood. It is albuminous in nature and
contains a small amount of coloring matter of a fatty nature. It holds in solution three proteids—fibrinogen, serum
globulin, and serum albumin.
Second, the organized parts, or the cellular structure (Fig. 74, Nos. 1 to 21). The cells float in the plasma and
consist of three groups: the erythrocytes, or red blood cells, the leucocytes, or white blood cells, and the
thrombocytes.
Erythrocytes.—The average number of red cells (Fig. 74, No. 21) of the domestic fowl range between
3,000,000 and 4,000,000 per cubic millimeter. The red blood cells are flattened and elliptical in shape, and possess
an oval elliptical nucleus. The average length is ¹⁄₂₁₀₀ inch and the diameter ¹⁄₃₈₀₀ inch, or 7 to 8 micra in diameter
and 12 to 13 micra in length. However the diameters vary in different kinds of birds. The cytoplasm is yellow and
glassy, and the nucleus takes basic stains and appears somewhat picnotic.

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Thrombocytes.—The thrombocyte (Fig. 74, No. 19) is of about the same length as the erythrocyte but
somewhat narrower. The nucleus is round, stains purple with the Wright’s stain, and the chromatin material is
somewhat diffused. The diameter of the nucleus is nearly equal to that of the cell. The cytoplasm is pale and may
show vacuoles near the nucleus. They may contain small circumscribed red structures. They vary somewhat in size
and shape. There are in the domestic fowl between 45,000 and 55,000 per cubic millimeter.
Leucocytes.—There are, in the blood of the hen, 28,000 to 35,000 leucocytes per cubic millimeter. The
leucocytes may be divided into five distinct types. These are as follows:
Polymorphonuclear leucocytes with eosinophilic rods (Fig. 74, No. 2) are round and have a diameter about
equal to the length of the erythrocyte. The nucleus is polymorphous; that is, it has two or more lobes. The nucleus
stains a pale blue, and the chromatin is diffused. The cytoplasm is colorless with bright red staining spindle-shaped
rods. There are 28 to 32 per cent. of this type of cell in the blood of the hen.

Fig. 74.—Blood cells of the fowl. Wright’s stain. From a S.
C. Rhode Island Red cockerel. 1, Basophile (mast cell) with
lilac staining spherical granules. 2, Eosinophile with rod-
shaped acidophile bodies. 3 and 4, Eosinophiles with
acidophile staining round granules. 5, Eosinophile ruptured.
6, Mononuclear leucocyte with vacuoles in the cytoplasm. 7
and 9, Transitional leucocytes (first stage). 8, Mononuclear
leucocyte. 10, 11, and 12, Small lymphocytes. 13 and 14,
Large lymphocytes. 15, A lymphocyte. 16, Lymphocyte
(nucleus centrally located). 17 and 18, Transitional
leucocyte. 19, Thrombocyte. 20, Neutrophile
(polymorphonuclear). 21, Erythrocytes.

Polymorphonuclear leucocytes with eosinophilic granules (Fig. 74, No. 3 and 4) are of about the same shape and
size as the preceding. The nucleus is similar to the former except that it may appear slightly picnotic. The
cytoplasm stains not at all or faintly blue; it contains round or spherical granules which stain a dull red. There is
from 4 to 6 per cent. of this type of eosinophiles found in the domestic fowl.
Lymphocytes are round in shape and of about the diameter of the width of a thrombocyte (Fig. 74, No. 11). The
nucleus is round, staining somewhat purple, and contains a diffused chromatin material. The cytoplasm exists in
only small amounts; it lies to the side of the nucleus and stains a pale blue. This is the small lymphocyte. A similar
cell but much larger also exists. This is the large lymphocyte (Fig. 74, No. 13). There is from 40 to 44 per cent. of
the lymphocytes in the blood of the fowl. The small lymphocytes are most abundant.
Large mononuclear cells (Fig. 74, No. 6) either round or oval, in shape, whose diameter may be about that of an
erythrocyte and at times much larger. The nucleus may be round, oval, or irregular, and at times rather crescent or
U-shaped (Fig. 74, No. 17). The cytoplasm is abundant and completely surrounds the nucleus. The cytoplasm

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stains a paler blue than the nucleus. Both taking the basic stain as do the lymphocytes. These constitute 18 to 20
per cent. of the cells of the blood.
Mast cells or basophiles (Fig. 74, No. 1) are of about the same size and shape as the eosinophiles. The nucleus is
round or oval, and stains a very pale blue. The cytoplasm is colorless, mostly to one side of the nucleus, and
contains round or spherical purple staining granules. This type of cell constitutes from 2 to 4 per cent. of the white
cells of the blood.
Structure of the Red Blood Cell.—The red blood cell is composed of a spongy stroma holding in its meshes
the red coloring matter. The stroma, or framework, of the erythrocyte consists principally of nucleo-albumin; it
contains lecithin, cholesterin, and salts. The red matter consists of an albuminous crystalline substance called
hemoglobin, which forms about 90 per cent. of the total solid matter of the dried corpuscle. Each red cell offers a
certain absorbing surface for oxygen. As the blood circulates through the delicate walls of the lungs and the air-
sacs, it takes up oxygen; the blood at the same time delivers to the air carbon dioxid which has been brought from
the tissues where active cell metabolism has been going on. This oxygen taken up by the erythrocyte forms a loose
chemical union and is known as oxy-hemoglobin. In this form it is carried to the tissues of the body where it is
given up by the erythrocyte to the tissues where oxidation is going on.
Hemoglobin is a crystallizable proteid substance containing carbon, hydrogen, oxygen, nitrogen, sulphur, and
iron.
Formation of the Cells of the Blood.—The red blood cells are formed in the red marrow of the bone.
Polymorphonuclear leucocytes are formed in the red marrow of the bones, and the lymphocytes in the lymph
glands and lymph follicles.
The bird carries a normal body temperature of 105° to 107° F. The average temperature of 50 mature hens and
cocks was 106.8° F. The blood is of a deep red color.
Composition of the Blood.—The average composition of the blood of the domestic fowl as given by Owen, is
as follows:

Whole shed blood:
Water 780 parts
Clot 157 parts
Albumin and salts 63 parts

1000 parts

Moist blood cells:
Average total weight 456.69
Water 342.52
Solid matter 97.50

Plasma:
Total weight 543.30 parts
Water 495.72 parts
Solid matter 30.72 parts

Blood when drawn and allowed to stand soon coagulates. In the blood of birds this process is very rapid, the
blood coagulating, in most instances, in about one-half minute. Blood coagulates only in the presence of calcium
salts.
During life, the liquor sanguinis is termed plasma; but after it has been shed from the body and coagulation has
taken place, the liquid residue is called serum. Serum is plasma with its modifications as the result of coagulation,
and as this latter process is brought about by the production of fibrin, we may say that serum is plasma minus
fibrin-forming elements.
The proteids of the serum are serum globulin, serum albumin, and a ferment produced as the result of
coagulation. As fibrinogen is used up in the process of coagulation, it is not found in the serum, but there is in the
serum a proteid known as fibrino-globulin. This is produced from fibrinogen during the process of fibrin
formation. The following tabulation gives a clear idea of the difference between the proteids of plasma and of
those of serum:

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Proteids of Plasma
Fibrinogen
Serum globulin
Serum albumin

Proteids of Serum
Serum globulin
Serum albumin
Fibrin ferment (nucleoproteid)
Fibrino-globulin

Fibrinogen is the precursor of fibrin.
The fibrin of the blood clot of the bird is soft and very lacerable. The
serum is usually yellow.

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THE FATE OF THE ERYTHROCYTE OF THE FOWL

The power of vascular endothelium to ingest red blood corpuscles has
been studied by Keys.
When bacteria or other minute foreign bodies are injected into the blood
stream of pigeons, they are rapidly withdrawn from the circulation into the
tissues of the liver and of the spleen. The foreign bodies are noted to be
contained within cells of a distinct type, which is found in both liver and
spleen. This type of cell contains, in addition to the foreign substances
injected, much yellow pigment, and when tested for iron by Pearl’s method
gives a positive Prussian-blue reaction.
In such specimens there is a display of contrast to other tissues. There is
an extensive content of cells possessing the distinct tone of Prussian-blue
iron reaction. These cells are distributed rather evenly throughout both the
spleen and the liver, but more numerously in the liver.
In the liver, under low-power magnification, these cells appear as blue
patches, sharply differentiated from the red-stained parenchyma. These cells
are larger in their greater diameter than the liver cells. They vary much in
size and form. They bear a constant relationship to the venous capillaries,
and often appear to occupy the lumen of the vessels. Under higher
magnification it is noted, however, that each cell is an integral part of the
endothelial intima lining of the capillaries. They are therefore fixed tissue
cells, engaged by one of its surfaces upon the reticulum of the vessel wall,
with a free surface bulging a greater or less degree into the lumen of the
vessel. The attached surface of the cell follows exactly the line of the vessel
wall. These cells are similar to those described for mammals by Kupffer
and are called Kupffer cells or stellate cells. In the fowl Keys proposes the
name hemophages. The nucleus of the hemophage stains a deep garnet with
the carmine used in the above-given technic, and contains two or three very
distinct and intensely stained nucleoli. In the hemophages, which are more
nearly flat, the nucleus appears like those of the typical endothelial cells;
whereas in the protruding hemophages of greater bulk, the nucleus is more
vesicular and is irregularly pyramidal in form. Rarely two nuclei are found
in one cell. Within this cell may be seen vacuoles of the cytoplasm which

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contain red blood corpuscles. These blood corpuscles have been phagocyted
from the circulating blood stream. Approximately one-third of the intimal
cells are hemophages. Each hemophage displays evidence that it contains,
or has recently contained, one or more red blood cells. The cell body of the
hemophage has no fixed morphology, but changes from time to time
according to its phase of phagocytic activity. In a stage which the
hemophage has recently ingested a red blood cell, the cell body bulges out
into the lumen of the vessel and the nucleus is crowded to one side. At this
time the red blood cell appears as those in the blood stream and possesses
the characteristic staining reactions. The nucleus of the red blood cell stains
deep reddish brown and the cytoplasm an even yellow bronze. In the next
stage the cytoplasm of the hemophage gives a diffuse Prussian-blue
reaction. Then in hemophages which represent later stages there are various
stages of disintegration and digestion of the red blood cell. The first
changes of the phagocyted red blood cell is hemolysis, the hemoglobin
escaping into vacuoles of the cytoplasm of the phagocytic cell, leaving the
nucleus-containing stroma distinctly outlined. The stroma may retain the
original ovoid form or may become spherical; the nucleus in such instances
remains ovoid. Gradually, both the stroma and nucleus lose their staining
reaction until finally the vacuoles contract about a small indistinct remnant
of the nucleus, which in its turn ultimately disappears. During this latter
process the size of the hemophage gradually decreases. The hemoglobin,
which has escaped into the cytoplasm of the hemophage, is seen to undergo
a series of changes. At first the greater part of the pigment does not give the
iron reaction but retains its yellow-bronze tone with erythrosin and occupies
vacuoles of various sizes. Later the contents of the vacuoles give the iron
reaction and with increasing intensity. Later there is a gradual decrease in
the staining reaction indicating that the iron gradually disappears from the
cells which extracted it from the red blood cells it digests. As a summary we
find, that these cells take care of the worn out red blood cells. They devour
them; hemolyze them, destroying the stroma and nucleus; split the
hemoglobin and free the iron; and then finally return to their normal form.
The spleen contains the same type cells, but they are fewer in number.
For the most part they are confined to the pulp cords and have no such
evident relation to the vessel wall, or lumen, as in the liver.
The function of the cells of the spleen are essentially the same as those in
the liver.

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Iron freed from the worn out red blood cells is not retained by the cells
freeing it, nor is it found in the bile. It does not occur elsewhere in the
tissues of the liver and spleen. It is possibly discharged into the blood
stream, and transported to the hemapoietic tissues. Cells which hemolyze
red blood cells and liberate the iron are to be seriously thought of in
connection with bile formation since bilirubin is approximately, if not
identical with, iron-free hematoidon.

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NEUROLOGY

The Nervous System.—The nervous system is an apparatus by means of
which animals appreciate and become influenced by impressions from the
outer world. Animals react on these impressions, and thus are enabled to
adapt themselves to their environment. This system is the organic
substratum of life, sensation, and motion. Broadly stated, the nervous
system connects the various parts of the body with each other, and to
coördinate the parts into a harmonious whole in order to carry on the bodily
functions methodically and to control the physiological division of labor
throughout the organism.
The nervous system consists of two parts. The first is the cerebro-spinal
system, which comprises the central nervous axis, including the brain and
the spinal cord, and the peripheral nerves, including the cranial and the
spinal nerves. The second is the sympathetic nervous system. The two parts
of the system are closely linked together, and both terminate in peripheral
nerve endings, including those of special sense, of sensation, and of motion.
The cerebro-spinal nerves especially preside over the special senses,
motion and sensation; and the sympathetic over the digestive, the
pulmonary, and the vascular apparatus.
From a structural standpoint, the nerve system consists of cell elements
peculiarly differentiated from all other tissue cells in that their protoplasm is
extended in the form of processes, often to great distances from the nuclear
region. The cell elements are held in place by supporting tissue and receive
an abundant blood supply; they are partly of ectodermal and partly of
mesodermal origin.
The cell element of the nerve system, called a neurone, is the
developmental, structural, and functional unit of the nervous system. It is a
single cell presenting unusual structural modifications. It comprises not

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only the nerve cell body with its numerous protoplasmic processes, or
dendrites, but also the axone, which may vary in length from a fraction of a
millimeter to fully half the bird’s length. The bulk of the axone is many
times the bulk of the cell body.
Certain non-medullated axones are surrounded by a delicate,
homogeneous, nucleated sheath, called the neurilemma, or sheath of
Schwann.

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THE CRANIAL NERVES

The cranial nerves have their origin in the brain and leave the cranial
cavity in pairs. They are numbered numerically from before backward,
there being twelve pairs in all. The following is a tabulation according to
their number, name, and function:

No. Name Functional Nature
I. Olfactory Smell-sense
II. Optic Visual-sense
III. Oculomotor Motor to muscles of eyeball and orbit
IV. Pathetici Motor to superior oblique muscle of eyeball
V. Trifacial Mixed: Sensor to face and tongue. Motor to face
VI. Abducentes Motor to External rectus of eyeball
VII. Facial Motor to muscles of head and face
VIII. Auditory Hearing-sense
IX. Glosso- Mixed: Tongue, pharynx and muscles of throat
pharyngeal
X. Vagus Mixed: Sensori-motor to respiratory tract and part of alimentary
tract
XI. Spinal accessory Motor to muscles of pharynx, neck and heart
XII. Hypoglossal Motor to muscles of the tongue

Olfactorius.—Nervus olfactorius (Fig. 75, C, 16). This is the nerve of
smell, one of the nerves of special sense. The organ of smell consists of five
layers as follows:
First, a layer of olfactory fibers extending in different directions and
consisting of a dense plexiform arrangement of the axones of the olfactory
cells. From this layer the fibers pass into the layer of olfactory glomeruli
where their terminal ramifications mingle with the dendritic terminals of
cells lying in the more dorsal layers, to form distinctly outlined spheroidal
or oval nerve fiber nests, the olfactory glomeruli.
Second, a fine granular layer of basic substance containing round cellular
structures, the stratum granulosum.
Third, broader granular, or molecular layer, having on its inner surface a
row of large pyramidal cells which are both small and large and which send

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their dendrites into the olfactory glomeruli. Their points are directed
outward.
Fourth, a layer of round cells tightly pressed together and measuring
about 5 microns in diameter. Between these cells are very fine nerve fibers.

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Fig. 75.—The brain of a hen.
Photograph.

A. Upper surface of the brain. 1,
Medulla oblongata. 2, Calamus
scriptorius. 3, Cerebellum. 4, Optic
lobes. 5, Transverse fissure. 6,
Longitudinal fissure. 7, Upper surface
of the left cerebral lobe. 8, Upper
surface of the right cerebral lobe. 9,
Lateral pillar of the cerebellum.

B. The posterior surface of the eyeball.
10, The sectioned surface of the optic
nerve.

C. The inferior surface of the brain. 11,
Corneo-scleral juncture. 12, The cornea.
13, The sclera. 14, The optic nerve. 15,
The optic chiasm. 16, The olfactory
lobes. 17, The medulla oblongata. 18,
Tuber cinererum et infundibulum.

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Fifth, a layer of epithelial cells.
The peripheral fibers and the nerve cell layers near the hemispheres
disappear so that the basic substance of the trabecula with the hemispheres
form the entire lobe mass. On the lower surface of the hemispheres there is
a long bundle of nerve fibers which enter into the substance of the olfactory
lobes and there disappears. These fibers are medullated. Non-medullated
fibers enter into the makeup of the olfactory trunk.
The original center of the olfactory nerve is not in the hemisphere, but in
the same location as the optic nerve. This nerve trunk consists of very fine
non-medullated fibers. The nerves of smell are therefore not peripheralistic
nerves. The nerve fibers are distributed to the mucous surface of the
turbinated bones. Toward the front they form an expanded prolongation.
The olfactory nerve, as it emerges from the cone-like anterior tip of the
cerebrum, is of considerable thickness and extends along with the median
dorsal artery of that region above and to the inside of the orbit, under the
thin bony structure. Before its termination into the posterior turbinated
bones, it is crossed by the superior maxillary division of the fifth pair of
cranial nerves. It extends as far as the pituitary membrane of the turbinate
bones upon which its filaments are distributed radially.
The Opticus.—The nervus opticus (Fig. 75, No. C, 14) the second
cranial, is the nerve of sight. The optic lobe, or tuberculum bigeminum lies
at the base of the brain on each side of the optic tract.
From the optic lobes the two trunks pass forward along the under surface
of the cerebri, forming the optic chiasm at the hypophysis (Fig. 75, No. C,
15), at which point the nerve fibers originating from the right side pass to
the left, and vice versǎ. From the chiasm the true optic nerves pass forward
to the posterior surface of the eyeball. They are composed of a bundle of
very fine, marrow-like nerves. These fibers enter into the ganglionic cells of
the retina. By removal of the finely adherent neurilemma, the optic nerve is
seen to be composed of parallel, longitudinal lamellæ, the margins of which
are mostly free on one side.
The Motor Oculi.—The motor oculi (Fig. 62, No. C, 10), the third
cranial nerve is a motor nerve. It originates close to the base of the brain
behind the position of the hippocampus of mammals on the inner side of the
crus cerebri, and also on the inner somatic column close below and
somewhat aside from the aqueduct of Sylvius. The nerve leaves the brain

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cavity through a distinct foramen near the foramen opticum, and supplies
the following eye muscles: first, after entering the orbit, it sends a branch
upward to the inferior portion of the inferior rectus; then, it gives off the
thick ramus ciliaris. The trunk then extends under the optic nerve and
passes forward to innervate the inferior rectus, the internal rectus, and the
inferior oblique. A ciliary ganglion forms on the trunk.
The Patheticus.—(Fig. 62, No. C, 11) is a small motor nerve, originating
close to the sulcus centralis, in the circle of the center brain over the valve
of Vieussens, between the posteriors of the optic lobes. It extends in a
dorsal direction between the cerebellum and the lobus opticus, to the
posterior of the latter of which it then forms a loop ventrally. Lying close to
the optic foramen it passes through a fine opening into the eye cavity and
supplies the superior oblique muscle of the eye. During its course it passes
dorsally over the optic nerve, and then crosses dorsally over the ophthalmic
division of the fifth pair of cranial nerves and the internal rectus muscle.
The Trifacialis.—(Fig. 62, No. C, 12). This, the fifth cranial, is a mixed
nerve and is divided into two parts, portio major and portio minor.
The portio major originates in the ganglion cells of the posterior part of
the brain. Commencing near the medulla oblongata it passes through the
posterior part of the brain, then upward and outward; and along its route it
forms the Gasserian ganglion, which lies partly in the cranial cavity or in its
wall.
The portio minor consists of the downward passing fibers containing the
motoric elements which are distributed to the muscles of the jaw and of the
eye. The roots are found in the ganglion from the center and back brain,
close below the pathetic nerve origin, where the pathetic passes between the
lobus opticus and the pars peduncularis; it then takes a lateral course
between the two.
The fibers of the portio minor do not take part in the formation of the
Gasserian ganglion, but are only partly surrounded by it.
There are three nerve trunks given off of the trifacialis: the ophthalmic,
the superior maxillary, and the inferior maxillary.
The ophthalmic division of the fifth nerve is the smallest of the three
branches. It emerges directly from the Gasserian ganglion, and passes
through a narrow bony canal in the base of the brain, below the pathetic and
the abducens, and through the foramen ophthalmicum. It then enters the eye

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cavity above the optic nerve, and on the wall of the cavity extends
downward, and with regard to the eyeball, dorsally lying close to the rectus
internus muscle and close to the surface of the eyeball. It passes along the
olfactory nerve, extends under the superior oblique muscle, and finally
reaches the inner angle, or canthus, of the eye. It here divides into the
recurrent externa and the ethmoidalis. The ethmoidalis branch is a straight
continuation of the ophthalmic. It extends along close to its fellow of the
opposite side, and, over the vomer, splits into two branches. The smaller of
these branches breaks through the bone cells of the jaw, continues upon its
ventral surface in a furrow extending forward, and terminates in the gum
region. It supplies the gum and point of the beak. The larger branch enters
into the cell substance extending to the tip of the beak, in its course sending
out a number of fine filaments, which spread out along the outer surface. At
this point these two branches may fuse. The larger branch is endowed with
the sense of touch.
The recurrent externa divides shortly after leaving the main trunk of the
eye cavity passes over the lacrimal gland. It gives two branches to this
gland and one to the membrana nictitans, and innervates the upper eyelid. It
then emerges from the eye cavity, passing over the os lacrimale, and gives
one or more branches to the integument of this region, including the comb.
This branch is large in birds with a large comb. Branches pass in front of
the lacrimal bone through the outer nasal cavity and into its deeper
structure.
Shortly after the ophthalmic branch has entered into the eye cavity and
before it crosses the optic nerve, it gives a fine branch to the motor occuli.
The second and the third branches of the fifth cranial nerve are mixed.
They contain elements of both the portio major and the portio minor. These
two branches come from the lower part of the outer region of the ganglion,
and pass together through a cavity which is located between the os
petrosum and alæ and basis sphenoid, and then branch.
The ramus secundus, or superior maxillary division, of the trifacial, is the
second branch and passes into the orbit below the optic nerve and the
eyeball. It is called the recurrent infra-orbitale. It gives an ascending branch
to the gland of Harder, one to the conjunctiva, one to the membrana
nictitans, and one to the eyelids. It also gives a branch to the skin below the
eye and to the angle of the mouth. This latter branch is called the recurrent

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subcutaneous. These two branches communicate with the recurrent nasal
ciliaris of the first trigeminus branch. The second branch passes below the
nasal opening, then passes on and forms the alveolar nerve on the side
between the gums. It sends several recurrent posterior branches to the
elevations on the back part of the mouth. It extends forward to the point of
the beak.
The inferior maxillary division of the fifth is larger than the other two. It
is directed downward and outward then upward to the temporal region. At
the temporal region it divides into five parts. It gives a branch to the
temporalis muscle, one to the pterygoid muscle, and one to the mylo-
hyoideus. The main branch gives twigs to the parotid gland region and
enters into the dental canal of the lower jaw. Numerous filaments break
through the lower jaw bone, and then spread out on the skin and rim of that
bone. The largest branch, called the recurrent maxillaris externa, comes out
near the coronoid process. The rest of the trunk extends to, and comes out
of, several foramina at the anterior point of the jaw bone.
These filaments are contained in grooves or cavities of the lower jaw and
terminate in touch buds.
The trifacialis fuses with the other cranial nerves and with the
sympathetic nervous system. Some of these fusions are as follows: The
recurrent ophthalmica fuses with the orbito-nasalis ganglion. Indirect fusion
of the recurrent maxillary division of this nerve takes place near the
Gasserian ganglion through the sympathetic nerves, the temporo-lacrimalis,
the facial nerves, the large cervical ganglion, and indirectly with the glosso-
pharyngeal and the vagus. This fusion has been called the superior recurrent
branch of the trigeminus, or trifacialis.
There is a direct fusion of the superior recurrent maxillary division of the
fifth just before entering the upper jaw. This fusion is with the spheno-
palatine ganglion and the sympathetic carotidis cephalica, and also with the
large cervical ganglion.
The Abducens (Fig. 62, No. C, 13).—This nerve originates in the
somatic and motoric column along with the other nerves of the eye muscles.
Its nucleus lies in the circle of the pars commissuralis of the cerebellum.
The nerve then passes ventrally, as does the motoris oculi and leaves the
brain along the median line. This is a comparatively large nerve and passes
somewhat laterally and ventrally from the foramen opticum through a canal

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in the sphenoid. It then enters the orbital cavity. Some muscular twigs are
given off to the quadratus and to the pyramidalis muscle. This nerve also
innervates the external rectus muscle of the eye. The abducens anastomoses
with the ramus ciliaris and the ophthalmic nerve and gives fine nerve twigs
to the ramus ciliaris externus of the ciliary ganglion.
The Facialis and the Acusticus.—The facial nerve originates with the
auditory (Fig. 62, No. C, 14 and 15) in a very vaguely known manner, from
the cerebellum. It divides into three parts.
The first of these probably comes from the complex ganglion with the
posterior roots of the auditory. This part belongs to the somatic sensory
group of nerves. From this same group originates the auditory, which
spreads out into the cochlea and takes the impressions of sound. This nerve
is short and thick, and, at the point where it loses its medullary covering on
entering the cochlea, there is developed a ganglion. This ganglion is similar
to the spinal ganglia.
The second part is provided with one root which originates mesially and
ventrally, from the deeper ganglion cells. Some of the fibers from this root
constitute the vestibular branches. They accompany the auditory and supply
the anterior part of the ear labyrinth and the semicircular canals. The larger
part of the fibers of this trunk make up the intermediate part of the facial.
The geniculate ganglion is formed at their fusion. The sympathetic spheno-
palatine nerve emerges from this ganglion, coming out of the aqueduct of
Fallopius.
The third part, called the portio dura, is the main facialis. It is located
opposite the auditoria intermedia. Its roots may be traced to the complex
ganglion, from which they take a direction ventrally from the median
portion.
The facialis, after emerging from the aqueduct of Fallopius, takes a
curved course and partly fuses with the sympathetic temporo-lacrimalis on
the upper posterior wall of the ear drum. It is here accompanied by the
carotid and the cephalic arteries. It leaves the ear drum through an opening
in the quadrate bone, giving off a large branch to the digastricus muscle and
a small one to the stapedius of the columella auris. The facialis trunk is
quite large. It then passes downward along the quadrate bone, where it
receives a large branch from the glosso-pharyngeus. This nerve also gives
branches to the mylo-hyoideus and the stylo-hyoideus muscle, crosses

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laterally the glosso-pharyngeus, and finally fuses with branches of the
subcutaneous and with the first, the second, the third, and the fourth
cervical nerves. After this fusion the nerves innervate the skin of the
anterior of the neck and the constrictor colli muscle.
The facialis anastomoses as follows: with a fine branch of the
sympathetic temporo-lacrimalis, indirectly with the ramus trigeminus, with
the large cervical nerve ganglion and with the spheno-palatine ganglion and
nerve.
The Vagus Group.—The ninth, the tenth, and the eleventh cranial nerves
are by some anatomists called the vagus group, first so called by Willis.
They are made up of both sensory and motor nerves.
The Glosso-pharyngeus.—The roots of the glosso-pharyngeus (Fig. 62,
No. C, 16; Fig. 76, No. 13) emerge, along with those of the vagus, from the
medulla oblongata, and enter, as a short trunk, the foramen jugulare et
caroticum. Between these two nerves there is usually found a thin portion of
bone. The trunk of the glosso-pharyngeus forms a ganglion in the foramen
jugulare et caroticum where it receives connecting branches from the near-
by ganglion radicis and vagus nerve. The glosso-pharyngeus passes out of
the foramen jugulare et caroticum above the large superior sympathetic
nerve ganglion, with which it communicates. The glosso-pharyngeus passes
diagonally over the ramus temporo-lacrimalis of the sympathetic system,
and then receives a very strong branch from the vagus (Fig. 76, No. 12). It
sends a short branch to the recurrent lacrimalis of the sympathetic system.
At this point there is formed a reddish-yellow ganglion, the petrosal
ganglion, which is similar to the petrosal ganglion of mammals. Frequently
it is found close below the large superior cervical nerve ganglion. The
petrosal ganglion is frequently connected by special fibers with the cervical
nerve ganglion, the large superior cervical nerve ganglion and the ganglion
radicis vagi. The glosso-pharyngeus is divided into the following branches.
First, the recurrent pharyngeus which gives branches to the upper part of
the throat and which is tortuous in its course. It receives a branch from the
superior cervical nerve ganglion and gives off branches to the salivary
glands and papillæ of the posterior tongue region.
Second, the recurrent lingualis, which passes with the lingual artery over
the hyoid bone to the base of the tongue and to the papillæ. Another branch

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passes below the tongue bone and supplies the tongue and the pharynx. The
glosso-pharyngeal is a mixed nerve.

Fig. 76.—Photograph of spinal cord of a hen. 1, Cerebrum. 2, The olfactory
nerve terminating at 3, the turbinated bones. 4, The superior maxillary division
of the fifth nerve dividing. 5, The eye with the upper part laid open. 6, The
cervical segment. 7, The lumbo-sacral segment. 8, The lungs. 9, The kidneys
lying above the peritoneum. 10, The terminal filament of the spinal cord. 11, The
hypoglossal nerve. 12, The vagus nerve. 13, The glosso-pharyngeal nerve. 14,
The branch from the vagus.

The Vagus.—The vagus, or pneumogastricus (Fig. 18, No. 5; Fig. 62,
No. C, 17; Fig. 76, No. 12), a mixed nerve, forms a ganglion in the foramen
through which it passes. The foramen lies between the os petrosum and os
occipitale, close to the foramen jugulare, above and to the inside of it.
The ganglionic root of the vagus communicates with the superior cervical
nerve ganglion. The vagus, after coming out of the foramen, takes up
branches of the spinal accessory, passes to the superior nerve ganglion,
crosses the carotid artery, and then, accompanied by the internal jugular, it
connects by a branch with the hypoglossal. It then communicates with the
petrosal ganglion, and receives a long branch from the superior cervical
ganglion. It then extends along the neck with the jugular vein and often
fuses with the sympathetic ganglionic plexuses. As it passes, it is
interwoven with the glosso-pharyngeus, but each nerve element retains its
own individuality. Extending down the neck, on entering the thoracic
cavity, it lies between the plexus brachialis and the carotid artery. Then it
passes below the subclavian artery, and between the bronchial tubes, the
aorta pulmonalis, and the subclavian vein. Then ventrally it rests upon the
glands, and the right and the left vagi fuse or unite. From here they radiate

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down to the stomach in fan-shape, and, continuing, they fuse with the
sympathetic system.
The other branches of the vagus are:
The first branch is the recurrent laryngeus, which supplies the lower end
of the bronchial tubes, and the esophagus, then enters above the bronchus
near the origin of the subclavian artery as the recurrent cardiacus.
The second are the recurrent pulmonale which pass into the lungs, each
fusing with its fellow from the opposite side, and giving off branches
inferior to the vena cava including a branch to the heart.
The third are the recurrent hepatici which pass through the diaphragm
and are distributed to the liver.
The Accessorius Spinalis.—This is a very small motor nerve (Fig. 62,
No. C, 18). It comes out between the dorsal and the ventral root of the third
cervical nerve. It lies close to the neck and extends anteriorly, receiving
roots from the first and the second cervical nerve. It passes through the
occipital foramen into the brain cavity and then enters the ganglion radicis
vagi. It passes out of the cranial cavity through the foramen jugulare. It then
partly fuses with the vagus and partly, as a fine branch, with the
subcutaneous colli.
The Hypoglossus.—The hypoglossus is a motor nerve (Fig. 62, No. C,
19). It originates anterior to the eleventh pair of cranial nerves, and from the
same ganglion as the abducens and the motor oculi. It leaves the medulla
oblongata from its ventral surface, and passes with a posterior and an
anterior branch out of the cranial cavity through two separate foramina in
the os occipitale laterale. The posterior branch, much smaller than the
anterior, passes between the cranial bones and the cervical sympathetic
nerve; it then passes at right angles through the rectus capitis anticus, and,
while closely following the carotid artery, it fuses with the anterior branch.
The larger, anterior branch, much stronger than the posterior, sends a short
strong branch to the complexus muscle. The rest of this branch, which
probably has sympathetic elements, is disposed as is a spinal nerve. It
crosses the sympathetic nerve, and at this point forms a typical cervical
sympathetic ganglion. It also forms a short loop with the recurrent ventralis
of the first cervical plexus. From this loop, after it has given off several
branches to the muscles of the neck, it gives off one or two strong branches,
which fuse with each other and with the posterior thin branch, thus forming

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the trunk of the hypoglossus. It receives many elements from the first
cervical nerves.
The hypoglossus sometimes communicates with the vagus, crosses over
the latter, and divides itself into two main branches, as follows:
First, the recurrent laryngo-lingualis, which passes between the cornua
of the os hyoideum and the larynx to the anterior part, and furnishes the
principal tongue muscles. It extends along the inferior surface of the tongue
and fuses with the one of the other side and extends to the free tip of the
tongue. This nerve probably receives sensory elements from the second root
and from the confluent of the first cervical nerve. This form of anastomosis
is well marked in birds with thick tongues, as ducks.
Second, the recurrent laryngeus furnishes the muscles of the superior
larynx and of the tongue skeleton. It extends downward and also furnishes
the muscles of the trachea. It follows the course of the jugular vein and at
the entrance of the chest supplies the furcula. The nerve passes into the
thorax, downward along the side of the bronchial tubes, and supplies
innervation to all the muscles of the inferior larynx.

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THE SPINAL CORD

Structure of the Cord.—The spinal cord is called the myelon or medulla
spinalis. It is a comparatively large, white, irregularly cylindrical cord,
flattened from above downward. It extends from the foramen magnum at
the base of the medulla to the caudal portion of the spinal canal where it
terminates in a fine filament. In order to allow considerable motion of the
spinal column without danger of injury to the spinal cord, the cord is
loosely suspended in the canal. The meninges, or coverings, are continued
from the brain. In addition to these there are to be found arteries, veins, and
nerves entering and others making their exit from the canal and from the
cord. At the cervico-dorsal juncture, where the brachial plexus is given off,
the cord is enlarged. There is another enlargement at the point where the
lumbo-sacral plexus is given off. At this point, superiorly, there is a
longitudinal cavity called the sinus rhomboidalis. This sinus contains a
gelatinous substance. There is a pair of nerves given off at each
intervertebral foramen. Thus there are as many pairs of spinal nerves as
there are vertebral segments. The inferior root is the motor root and carries
the impulses from the cord to the periphery. The superior root is the sensory
branch and carries the impulses from the periphery to the cord, and thence
the impulse is carried to the centers in the brain. The sensory and the motor
roots are of about equal size. The inferior have more numerous filaments.
The ganglion on the superior or sensory root is relatively large. In the sacral
region the sensory and the motor branches pass through their own bony
canal.
White rami communicantes are given off at each intervertebral foramen
to the sympathetic system and gray rami are received from the sympathetic
ganglia. Thus there is established a direct communication between the
sympathetic and the spinal system. There is a ganglion on the superior root
just outside the spinal cord.
The ganglionic portion, or gray matter, is arranged in the center of the
cord in two comma-shaped parts forming an X. The white matter, or the
material forming the fibers, is arranged around the central ganglionic
portion.

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The spinal cord may be divided into two lateral symmetrical halves.
There are two longitudinal fissures, one on the upper and the other on the
lower half. The upper called the superior median fissure is narrow but deep.
The one on the inferior side, called the inferior median, is usually more
pronounced. The superior parts of the gray matter are called the superior
cornua, or horns; the inferior parts the inferior cornua, or horns. The center
of the cord is pierced by a central canal which communicates with the
fourth ventricle at the calamus scriptorius.

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STRUCTURE OF THE NERVE TRUNKS AND GANGLIA

The protoplasmic processes called dendrites have a similar structure to
the cell body. The dendrites branch dichotomously, become rapidly smaller,
and usually end at no great distance from the cell body.
The axone or axis cylinder process, differs from the cell body and from
the dendrites. It does not contain chromophilic granules. It consists entirely
of neurofibrils and perifibrillar substance. It emerges from the cell at an
enlargement known as the axone hill. This hill is free from chromophilic
bodies.
Nerves are divided into two kinds, medullated and non-medullated.
Medullated nerves are divided into two kinds: medullated nerves with a
neurolemma, and medullated nerves without a neurolemma.
Medullated nerves with a neurolemma consists of an axone, a medullary
sheath, and a neurolemma. A delicate membrane called an axolemma, or
periaxial sheath envelops the axone. The medullary sheath called myelin, is
semifluid, somewhat resembling fat. The outer covering is the neurolemma,
or sheath of Schwann. It is a delicate, structureless membrane which
incloses the myelin. There is under this sheath an occasional oval nucleus.
At intervals there are constrictions, or nodes, called the constrictions of
Ranvier. The part between the nodes is called the internode.
The medullated axones without a neurolemma are the medullated nerve
fibers of the central nervous system.
The non-medullated axones, or non-medullated nerve fibers, are divided
into non-medullated axones with and those without, a neurolemma.
The non-medullated axone without a neurolemma is merely a naked
axone. They are confined to the gray matter and to the beginnings and
endings of sheath axones, all the latter being uncovered for a short distance
after leaving the nerve cell body and also just before reaching their
terminations.
The long axones serve to make connections with the peripheral, or
distant, nerve cell, muscle cell, or gland cell; while the shorter axones of
certain neurones divide into terminal branches in the immediate vicinity of

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its cell body, presumably to come into relation with other nerve cells in the
same or adjacent groups.

Page 303

Fig. 77.—Histological structure of
tissues.

1. Non-striated or involuntary muscle
cell. a. 1, Nucleus; 2, Protoplasm. b.
Transverse section showing nuclei in the
center of the cells that are cut through
the nuclear zone. c. A cross-section of
the connective tissue which binds
together the muscle cells. d. A section
showing the so-called intercellular
bridges.

2. A cross-section of the rectus
abdominalis. 1, The endomysium which
binds the cells into primary fasciculi or
bundles. 2, The perimysium which
surround the bundles of fasciculi. 3, The
epimysium which surrounds the muscle.
These binding structures are white
fibrous connective tissue.

3. A longitudinal section at the juncture
of a muscle and tendon. a, The juncture
between the muscle and tendon. Note
the many nuclei in both muscle and
tendon. This is voluntary or striated
muscle which make up the dermal,
dermo-osseous and skeletal muscles.

Page 304

4. A longitudinal section of heart
muscle. a, Connective-tissue cell. b,
Nucleus of a muscle cell. c, Cement line
between the muscle discs. d, The cell or
segment.

5. A bipolar ganglionic nerve cell. a,
The nucleus. b, The nucleolus. c, The
fibrillar structure. d, The medullary
sheath.

6. A diagram showing the scheme of the
peripheral nerve trunk. a, The neuraxis
of the peripheral sensory neurone. b,
The spinal ganglion of the superior or
sensory root. c, The dendrite or
peripheral nerve fiber of the sensory
nerve. d, The nerve trunk. f, The
sympathetic nerve ganglion connected
with the spinal cord through the white
and the gray ramus communicans. e,
The neuraxis of the sympathetic
neurone. g, Neuraxis or trunk of the
motor neurone or nerve cell. h, The
anterior horn of the gray matter of the
spinal cord.

7. A diagram of a peripheral sensory
neurone. a, The neuraxis which ends in
the spinal cord or brain. b, The T-shaped
division of Ranvier. c, The dendrite or
sensory nerve fiber in the nerve trunk. d,
The nucleus and nucleolus of the cell e.,
f. the axis cylinder process of the cell. g,
The telodendrions or terminal branches
of the dendrite or axis cylinder.

8. A schematic diagram of the sensory
motor reflex. a, The telodendria. b, The
dendrite. c, Nerve cell of the motor
neurone. d, The motor neurone. f, The
muscle fiber. g, The neuraxis of both
sensory and motor neurones, the upper
being the sensory. h, The nerve cell in
the sensory ganglion. i, The sensory
neurone or axis cylinder (nerve fiber). j,
The skin with peripheral telodendrion of
sensory neurone.

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Neurones are devoted to the maintenance of functions. Reproductive
neurones are so arranged as to receive afferent nerve impulses from other
tissues; emissive neurones give off efferent nerve impulses. The former are
sensory neurones; the latter are motor neurones if connected with muscles,
and excito-glandular if connected with gland cells. The basis, then, of the
nerve system is a series of neurones, with projecting and association
processes, coördinated for the purpose of performing specific actions
manifested either by motion, by trophic changes, or by the apperception of
stimuli of a chemic, mechanic (tactile and auditory), thermal, or photic
nature.
The whole of the nerve structure is composed of the nerve tissue and
supporting connective tissue. The neurones constitute the nerve tissue,
while the supportive tissue is composed of neuroglia and of white fibrous
tissue derived either from the investing membrane or from the sheaths of its
numerous vascular channels.
The neurones, or nerve cells, exhibit marked variations as to external
characters, dimensions, and form. The neurone presents a swollen cell mass
and a nucleus; it is known as the ganglion cell. From this cell body are
given off a number of processes of two distinct kinds: first, protoplasmic
processes, which are commonly branched, called dendrites; second, a
single, thinner, and paler process; the axis cylinder process.
The bodies of cells vary in size from 4 to 100 microns or more in
diameter. The largest cells occur in the inferior horn of the spinal cord, in
the spinal ganglia, in the large pyramidal cell layer of the cerebral cortex, in
the Purkinjean cell layer of the cerebellum, and in Clark’s column of the
spinal cord. Very small cells occur in the olfactory bulbs, in the granular
layer of the cerebral and cerebellar cortex, and in the gliosum cornuale of
the cord.
Nerve cells are classified according to the number of processes arising
from the cell body, and neurones are referred to as unipolar, bipolar, and
multipolar.
Unipolar cells are met with frequently in early stages of embryonic
development, but are rare in adults, occurring only in the retina, in the
olfactory bulb, and within the baskets of the Purkinjean cells of the
cerebellum. The cells of the cerebro-spinal ganglia, except the cochlear and

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vestibular, are apparently unipolar, but they are developmentally and
functionally of bipolar nature.
Bipolar cells are found almost exclusively in the peripheral sensory
system, as in the olfactory membrane, in the retina, in the cochlear and
vestibular ganglia, and in the cerebro-spinal ganglia of the embryo.
Multipolar cells are the most numerous and form the principal elements
of nerve centers throughout the system. They are termed multipolar because
of the greater or lesser number of dendrites given off in addition to the
single axone.
The body of the nerve cell consists of a mass of protoplasm surrounding
a nucleus. The cytoplasm of the nerve cell consists of two distinct
substances: first, neurofibrils; second, perifibrillar substance. In most nerve
cells there is a third substance called chromophilic bodies.
The neurofibrils, extremely delicate, are continuous throughout the cell
body and all of its processes. Within the body of the cell they cross and
interlace and probably anastomose.
The perifibrillar substance is a fluid or a semifluid substance which both
in the cell body and in the processes surrounds and separates the
neurofibrils.
The chromophilic bodies are granules or groups of granules which occur
in the cytoplasm of all the larger and of many of the smaller nerve cells.

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THE SPINAL NERVES
The first pair of spinal nerves come out between the atlas and the
occipital bone. Each nerve divides into three branches. The first is the
anterior branch which innervates the dorsalis, the biventer cervicis, the
cervicales, and the caput posticus muscles. The second is the recurrent
ventralis which passes mesially and downward from the recurrent
communicans. It innervates the rectus capitis anticus muscle and joins a
branch of the hypoglossal nerve. There is given off a white ramus
communicans to the sympathetic nerve.
The second spinal nerve emerges from the opening between the first and
the second cervical vertebræ and is similarly disposed as the first cervical. It
gives off a branch called the recurrent ventralis which fuses with branches
of the first cervical and the hypoglossal nerve. This nerve innervates the
complexus muscle.
The succeeding cervical nerves emerge in a similar manner down the
neck and are distributed to the muscles and other structures of the cervical
region. The second, the third, and the fourth cervical nerve gives off
branches which form anastomosing loops with the facial nerve.
According to Gadow the last cervical nerve passes between the last
cervical and the first dorsal segment. There are thus fifteen pair of cervical
nerves.
The first pair of dorsal nerves pass out between the first two dorsal
vertebræ. The first few dorsal nerve branches innervate only the trunk
muscles. Other branches supply the skin and the other adjacent integument.
The ventral branches of the cervical nerves often communicate with the
ventral branches of the first dorsal nerves. These branches are larger than
the superior branches and aid in the formation of the brachial plexus.
Smaller inferior branches are distributed to the scalenus and other muscles,
and extend as far posterior as the intestines.
The dorsal branches of the spinal nerves in the lumbo-sacral region are
very small, on account of the lack of extensive development of the muscles
of this region. The elements entering into these nerve trunks are largely
vasomotor nerves. In addition to the upper twigs supplying the skin and the

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other integument of the region, other branches descend into the abdominal
cavity.
The caudal spinal nerves are not well developed and disappear in the
region of the caudal vertebræ. The dorsal branches innervate the levator
muscles, and the ventral branches the depressor muscles.
There is thus given off, throughout the vertebral column, a pair of nerves
between each two vertebral segments, making as many pairs of nerves for
the region as there are vertebral segments of that region.
The Brachial Plexus.—The brachial plexus (Fig. 73, No. 19) arises
principally from the roots of the last three cervical and the first dorsal spinal
nerves. These branches anastomose beneath the deep face of the scapulo-
humeral articulation.
The brachial plexus divides into two distinct parts. The first (Fig. 73, No.
20) the dorsal called the superior thoracic is distributed to the serratus and
the rhomboideus muscle. The second is the inferior thoracic (Fig. 73, No.
21), which consists of the main plexus, and which gives off muscular
branches especially to the sterno-coracoideus and to the main portion
passing on as the nerve trunk to the structures of the wing.
From the superior thoracic plexus there are several secondary plexuses
formed.
The dorsalis or serratus plexus. This plexus is located adjacent to the
anterior part of the main plexus and is formed of from two to four spinal
nerve branches. The rhomboideus is supplied by branches which may be
traced to the first root of this plexus. This nerve is called the rhomboideus
superficialis. Another nerve is given off from the middle part of the dorsal
side of the plexus and is called the rhomboideus profundus. A third, the
superficialis serratus, is the largest of the branches. It breaks up into
terminal branches, one going to each serration, or digitation, of the serratus
muscle. Branches from the anterior portion of this plexus are distributed to
the patagii muscles.
The superior brachial plexus gives off the following nerves:
The subcoraco-scapularis, which is purely a motor nerve, springs from
the anterior roots of the plexus. It gives off a branch to the following three
muscles: subcoracoideus, subcoracoido-scapularis, and scapulo-humeralis.
The scapulo-humeralis is distributed to the scapular humeral region.

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The latissimus dorsi is located on the peripheral border of the scapulo-
humeralis or supraspinatus. It originates from the second, and the fourth
nerve roots of the plexus. It is located on the dorsal side of the plexus. It
divides into two main branches, one going to the latissimus dorsi and the
other to the scapulo-humeralis muscle. From the side are given off branches
which supply the patagii muscle and enter into the formation of the dorso-
cutaneous plexus.
The axillaris springs from the second and the third root of the brachial
plexus, extends in a lateral direction, passing the ventral and distal rim of
the insertional part of the posterior scapulo-humeralis or teres et
infraspinatus and enters near the capsular ligament of the shoulder-joint. It
gives off to this joint a small branch, called the recurrent articularis, which
passes outward between the triceps brachialis and the humerus. It lies on the
inner side of the major deltoid, and patagii muscles, and also the skin of the
lateral shoulder and the upper arm region. The recurrent axillaris
communicates with the main branch of the radial nerve.
The cutaneus brachii superior is a small nerve which springs from the
last brachial plexus root and passes between the skin and the triceps brachii
muscle on the dorsal surface of the upper arm, or brachial, region. It
extends down over the elbow region, where it gives off numerous branches
to the skin of these regions, to the meta-patagium and to the extensor
muscles of the upper arm.
The brachialis longus superior is a large nerve trunk which springs from
most of the other plexus roots. It extends around to the dorsal side of the
upper arm and supplies the skin, the feathers, and the muscles of the
forearm and the hand. Branches from this nerve trunk supply the triceps
brachii and other muscles of the region. The main branch passes between
the radius and the ulna, and, passing the elbow-joint, gives off branches to
that joint. Passing on, it divides into two branches. One of these extends
superficially over the upper part of the condylus ulnaris and supplies the
extensor digitorum communis and the extensor metacarpi ulnaris, or flexor
metacarpi radialis muscles, and, continuing superficially to the ulnar side, is
distributed to the skin of the region. The second, a deep branch, extends on
the ulnar side of the radius over the extensor indicis longus, and innervates
the latter muscle, the extensor pollicis longus, the extensor pollicis brevis,
the adductor pollicis, the interosseous palmaris, and the flexor digitorum.

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The inferior brachial plexus gives off the following branches:
The supra-coracoideus, a large nerve which springs from the first main
root of the plexus, and passes outward through the foramen coracoideum of
the sternal ligament.
The sterno-coracoideus, a small nerve which extends downward from the
plexus.
The somewhat large posterior coraco-brachialis, nerve which springs
from one or two middle roots of the plexus and accompanies the pectoral
nerve.
The anterior thoracic, a large nerve which springs from two or three of
the posterior roots of the plexus and extends to the shoulder cavity where it
branches. The anterior branch is distributed to the patagium and the front
part of the pectoral muscles. The posterior branch supplies muscles along
the side of the thorax and extends into the abdominal muscles.
The anterior coraco-brachialis, a small nerve which springs mostly from
the inferior longus brachialis, passes to the distal end of the tuberculum
humeralis radii, then passes backward between the front part of the humerus
and the biceps, where it supplies the anterior coraco-brachialis.
The cutaneous brachialis et inferior brachialis, a small nerve which
springs from the posterior roots of the plexus. It is distributed to the skin of
the region and branches are given off to the patagii and the ventral wing
surface. A few branches extend as far as the upper arm.
The brachialis longus inferior (Fig. 68, No. 2), a continuation of the
main trunk of the inferior brachial nerve, which comes out of all the plexus
roots except the first. It gives off some branches to the pectoral region and
then enters the shoulder cavity. It gives off the anterior coraco-brachialis,
passes down the humerus in an S-shape, and divides into two branches, the
ulnar and the median.
The ulnar nerve (Fig. 67, No. 3) divides into numerous branches which
are distributed to the ulnar side of the forearm and the hand. The ulnar
nerve passes below the skin of the ulnar outside rim of the forearm and
gives branches to the carpi ulnaris, finally supplying the flexor digitorum; it
then passes with the tendon of this muscle downward to the interosseous
dorsalis, the abductor indicis, or flexor minimi brevis, the flexor pollicis,
and the abductor pollicis, or extensor proprius pollicis.

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The median nerve (Fig. 67, No. 2) extends down the arm and gives
branches to the biceps muscle, and to the patagii region. Continuing, the
median nerve supplies the pronator muscle and the brachialis inferior, or
brachialis anticus, and then divides into two branches. The first and largest
branch passes between the two pronator muscles giving branches to the
pronator profundus, or pronator longus, and the flexor digitorum profundus
muscle. This nerve then passes anteriorly along the tendon to the base of the
digit, and, on the dorsal side, joins the other branch of the median nerve. At
this point there is often a plexus, and at the point of fusion of the ulnar
nerve on the ulnar side there may also be a small plexus. These plexuses
mainly supply the skin of these regions. The second branch, passes forward,
crosses the extensor carpi radialis and lies just below the pronator
profundus, or pronator longus, giving branches to the skin. It passes
downward on the radial side of the ulnar and supplies the muscles of that
part; it then continues down the hand. Branches are given off to the extensor
proprius pollicis, the interosseous dorsalis, the flexor digitorum, and to the
skin between the thumb and the forefinger.
The intercostal nerves (Fig. 70, No. 18) are given off from the spinal
cord of the dorsal region. The superior branches are small and supply the
superior dorsal region. The inferior branches lie one behind each rib,
innervate the intercostal muscles, and give a few twigs to the superficial
thoracic muscles.
The Lumbo-sacral, or Crural, Nerve Plexus.—The crural plexus (Fig.
70, No. 35 and 36) is made up of trunks from the last two lumbar and first
four sacral spinal nerves. There are two portions of this plexus separated by
a considerable distance.
The anterior portion (Fig. 70, No. 35) consists of the lumbar nerves and a
portion of the first sacral nerves. The fusion takes place on the bony ridge
that separates the lumbar from the sacral region.
The posterior portion (Fig. 70, No. 36) consists of a part of the first sacral
and all of the three succeeding nerves.
The anterior nerve of this plexus is distributed to the abdominal muscles.
An anterior branch is given off to the sartorius. A large cutaneous branch
enters between the sartorius and the ilio-trochanteric eminence, and
supplies the outer and the upper surface of the upper thigh region. Several
short branches are given off from the middle, or main, mass of the crural

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plexus to the ilio-trochanteric, or gluteal, muscle. Another nerve passes over
the side of the sartorius adjacent to the femoro-tibialis, or extensor femoris,
and supplies the ilio-tibialis, or gluteus primus. The rest of this section of
the crural nerves pass in a distal direction over the inner and front side of
the cutaneous nerve and enter the ilio-femoralis, or gluteus medius, the
ambiens and the femoro-tibialis muscle.
The furcalis nerve comes out between the last two lumbo-sacral
vertebræ.
The obturator nerve springs from several roots. The anterior root of this
nerve comes from the main trunk of the crural plexus, and its last root from
the furcalis nerve. The obturator nerve extends in a ventral direction from
the plexus, then horizontally on the inner surface of the abdominal cavity. It
gives off twigs to the obturator muscle and then passes through the
obturator foramen. After leaving the abdominal cavity it gives branches to
the accessorius, the obturator, and, the pubio-femoral, or adductor longus
muscle.
The crural plexus gives off another large nerve trunk which extends
downward. Shortly after emerging from the plexus it gives off a muscular
branch to the ilio-femoralis, or gluteus medius muscle. It then passes
between this muscle and the shaft of the femur, to the inner posterior
surface of the thigh, and to the inner surface of the knee. It gives off a
branch to the structures of the knee. At the knee this nerve terminates in
several branches, some of which pass to the inner surface of the tibial head,
the internal lateral ligament, the periosteum, the internal condyle, and
finally to the upper part of the head of the gastrocnemius muscle.
The main part of this nerve passes downward as the cutaneous nerve,
along the inner surface of the lower thigh.
The ischiadic plexus (Fig. 64, No. 41) has five to six roots, which fuse
into the ischiadic trunk. This main trunk extends out of the abdominal
cavity, through the ischiadic foramen, close behind the anterior trochanter
of the ilium (Fig. 65, No. 1). It gives a branch to the external ilio-femoral or
gluteus medius, and a branch to the post-acetabular portion of the ilio-
tibialis, or gluteus primus muscle. The main trunk (Fig. 69, No. 13) passes
downward to the lower portion of the thigh. In this course there are two
branches which run parallel to the femoral artery and the femoral vein. It
gives off a small muscular branch to the accessorius, and further down

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gives off a long slender branch to the outside of the knee-joint. It gives off a
lateral cutaneous branch (Fig. 66, No. 7) to the posterior outer portion of the
lower thigh. It supplies motor fibers to the external head of the
gastrocnemius muscle.
At the knee region the ischiadica divides into three parts. The largest
branch (Fig. 69, No. 14) passes with the tendon of the ilio-fibularis, or
biceps femoris muscle, through a loop, the biceps band, and lies on the
upper lateral surface of the fibula. It is covered by the external head of the
gastrocnemius muscle. It innervates the three posterior muscles of the lower
thigh, and then divides into two branches. One, the superficialis peroneus
(Fig. 69, No. 16) passes with the profundus nerve, forming a double trunk
and occupying the tibio-fibular groove on the antero-lateral side. It passes
over the transverse ligament and the tibio-metatarsal joint, and after sending
small branches to the structures of the tibial side of the metatarsus, it ends
as a cutaneous nerve on the upper side of the third and the fourth toe.
The other branch is the peroneus profundus, which separates from the
peroneus superficialis and passes downward in company with the tendons,
under the transverse ligament, and then along the anterior upper surface of
the metatarsus, where it innervates the muscles of that region. It gives
branches to the malleolus, to the tendons of the third toe, and to the median
part of the second toe, and supplies the cutaneous structures of the third and
the fourth toe.
The third branch of the ischiadica, a long nerve, is given off just after the
ischiadica passes through the loop. It passes downward between the two
peroneal nerves. It is covered by a sheath. It passes over the posterior
outside rim of the intertarsal joint and innervates the tendon sheath. The
main portion of this nerve is located on the anterior surface of the tendon
Achillis, and passes down on the plantar side, and innervates the periosteum
and all plantar foot muscles. It finally radiates to the plantar surface of the
three anterior toes.
The integument of the toes is sparingly supplied with nerves.
The nerve trunks that do not pass through the biceps band, or loop can be
divided into a medial (Fig. 69, No. 15) and a lateral (Fig. 69, No. 17)
portion. The medial portion (Fig. 69, No. 15) soon divides into numerous
branches which supply the muscles of the posterior and the inner portion of
the thigh. A rather large, long branch passes downward along the tendon of

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the plantar muscle, which lies on the posterior median edge of the tibia, and
gives off twigs to the median and posterior part of the intertarsal joint,
supplying the periosteum and other structures and the adjacent skin. It
passes downward along the outer side of the medial metatarsal insertion of
the tendon Achillis.
The fifth branch is given off from the second trunk and lies laterally. It is
covered by the external head of the gastrocnemius, passes along the vena
saphena, and gives off a short main branch to the inner side of the
intertarsal joint. The main part passes the tibial side of the joint, becomes
subcutaneous, and finally innervates the two plantar muscles. A lateral
ascending inner branch innervates the flexor perforatus digitorum, and, in
company with an outer branch, the external head of the gastrocnemius, and
also the flexor pedis perforatus.
The plexus pedundus is formed from the spinal nerves coming out of the
plexus ischiadicus. These fibers emerge caudalward and are directed
horizontally. They frequently anastomose with each other, especially on the
pubic rim and on the outside of the plexus ischiadicus. These branches are
deeply imbedded in the kidney substance and innervate the pubio-
coccygeus, or depressor coccygis lateralis, the ilio-coccygeus, the
transversalis, the sphincter, and other muscles of this region, and the skin of
the anal region.

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THE BRAIN

The Brain Coverings.—The cerebro-spinal axis of birds is similar to
that of mammals. The meninges of the brain are three in number, dura
mater, arachnoid, and pia mater. The dura mater is the thickest. It is
constructed of white fibrous connective tissue, and lines the cranial cavity.
Thus it serves as an internal periosteum. It is continuous with the spinal
dura mater at the foramen magnum, and is also prolonged as a sheath of the
nerves. In birds of flight where the air-sacs and reservoirs are developed to
the highest state, Sappy finds that, “just as the medullary tissue is replaced
by air in the bones of birds, so might it be imagined that the subarachnoid
fluid is also replaced by air around the spinal cord,” and observations justify
the correctness of this statement. The dura mater measures exactly the
volume of the marrow in birds; so that there does not exist between the
fibers and the nervous surface any space for an accumulation of liquid. This
anatomical fact is sufficient to demonstrate the absence of subarachnoid
fluid in the bird. In denying the existence of this fluid, it ought to be added
that in this class of vertebrates, the spinal prolongation is covered by a triple
envelope; and that between the pia mater and the dura mater is a thin
transparent membrane, which is lubricated by a serous fluid. This fluid
however does not collect; it only moistens the arachnoid membrane.
The arachnoid is located between the dura mater above and the pia mater
below. The pia mater adheres closely to the nerve tissue.
The falx cerebri exists in fowls and in turkeys. It has the form of a
segment of a circle, and extends from the middle of the interval of the
openings for the olfactory nerves to the tentorium cerebelli. The falx
cerebelli is absent. The tentorium is small and is sustained by a bony plate,
and there are in addition two folds, one on each side, that separate the
hemispheres from the tubercula quadrigemina. Owing to the absence of the
falx cerebelli, the meninges lie close together. The falx cerebri is ossified in
birds.
The Brain Structure.—The brain (Fig. 62, C and Fig. 75, A and C) is
made up of three principal parts: the cerebrum, the cerebellum and the

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medulla oblongata. In a fowl of medium size the brain weighs about 150
grains.
The pons varolii is absent in birds. The crura cerebelli (Fig. 75, No. 9) are
immediately connected with the corpora restiformia. The lower face of the
isthmus is convex posteriorly; in front, the tubercula bigemina (Fig. 75, No.
4) are united to each other by a comparatively large transverse cord, formed
by the optic nerves intercrossing in the median line. The superior face of the
medulla oblongata is depressed above to constitute a fourth ventricle; in
front of this ventricle are the tubercula bigemina, or optic lobes. These two
voluminous tubercles are separated from each other above, where they
embrace the cerebellum, and are salient on the sides of the lower face. They
are hollow internally, and communicate with the aqueduct of Sylvius. The
thalami optici are not well developed.
A large transverse fissure divides the cerebrum from the cerebellum (Fig.
75, No. 5). The optic chiasm (Fig. 75, No. 15) behind which lies the
hypophysis (Fig. 62, No. C, 20) covers the region of the middle brain. The
large transverse fissure is the dividing line between the hemispheres and the
optic lobes. If the hypophysis be removed there will be observed a slit
surrounded by gray matter which is called the tuber cinereum et
infundibulum (Fig. 75, No. 18). On the pars commissuralis and the after
brain there are visible the roots of the fifth, the ninth, the tenth, and the
twelfth pairs of cranial nerves. Close beside the median furrow which
extends to the front part of the long furrow of the spinal cord there is
observed the third pair of cranial nerves, which have their origin in the
middle brain. The fourth pair of cranial nerves extend from the roof of the
middle brain on both sides between the middle brain and the optic lobes.
These nerves finally emerge and become visible on the ventral surface.
The sixth nerve is visible near the middle furrow and almost in the
middle of the pyramids, and near the roots of the fifth, the seventh, the
ninth, the tenth, and the twelfth pair of cranial nerves.

THE DIVISIONS OF THE BRAIN

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(Thalamus

(Pineal body

(Infundibulum

(Hypophysis

Forebrain (Optic tract and chiasm

(Cerebral hemispheres

(Olfactory lobes

(Third ventricle

(Lateral ventricles

(Peduncles of the cerebrum

Midbrain (Optic lobes

(Aqueduct

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(Medulla oblongata

Hindbrain (Cerebellum

(Fourth ventricle

The medulla oblongata (Fig. 62, No. C, 1; Fig. 75, A and C) terminates
anteriorly in the pars commissuralis and the pars peduncularis. As the spinal
cord approaches the head there is a gradual swelling, or lateral thickening,
which merges into the medulla oblongata. The superior and the inferior
surface of the medulla oblongata (Fig. 75, No. A, 1 and C, 17) are flattened.
There is a shallow furrow and a slight swelling at the point where the
hypoglossal nerve emerges. The central canal of the spinal cord gradually
comes closer to the upper surface and communicates with the fourth
ventricle, at which point the posterior raphe is shortened and the sulcus
longitudinalis posterior becomes shallow. At the point where the central
canal terminates in the fourth ventricle there is a V-shaped point called the
calamus scriptorius (Fig. 75, No. 2). The fourth ventricle is located on the
upper wall of the medulla oblongata below the cerebellum, and is bounded
laterally by the peduncles of the cerebellum. It is marked posteriorly by the
calamus scriptorius and anteriorly by the valve of Vieussens.

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The valve of Vieussens is located at the posterior end of the aqueduct of
Sylvius. The posterior part of the fourth ventricle is marked by grooves or
furrows. Extending along the central part of the floor of the fourth ventricle
there is a sulcus, or groove, called the sulcus centralis, which divides the
superior pyramids. On the median lateral sides there are two points of gray
substance which form the alæ cinereæ. The roots of the pneumogastric, the
glosso-pharyngeal, and the spinal accessory may be traced to the alæ cineræ
and the gray matter of the ridges of the medulla oblongata. The sixth pair of
the cranial nerves emerge from the medulla near the sulcus centralis and to
the side of the auditory nerve. Part of the trigeminus emerges from the rim
of the furrow next to the ridge. At the outer border of the medulla are
observed the thick ends of the roots of the pneumogastric, the spinal
accessory, the glosso-pharyngeal, and the auditory facialis.
On both sides of the sulcus longitudinalis inferior are found the inferior
pyramids, or pyramidal columns. These pyramids become expanded near
the origin of the third pair of nerves and merge into the cerebral peduncles,
or crura cerebri.
The pyramidal fibers may also be traced to the optic lobes. The roots of
the abducens are found at a point between the crura cerebri and the optic
lobes. The third pair lies to the side of this, and the roots of the trigeminus
are adjacent to those of the third. A bundle of fibers from this region pass
into the cerebellum and form the crura cerebelli; others pass into the
cerebellum from the side, spreading out in fan-shaped radiation, and
forming the white central substances peculiarly arranged, called the arbor
vitæ, or tree of life. A third bundle fuse with the crura cerebelli anteriorly,
and pass into the peduncles of the cerebrum, or crura cerebri.
The gray ganglionic substance forms columns which extend the whole
length of the medulla oblongata and into the cerebri. The medulla oblongata
contains numerous centers which preside over various visceral functions as
deglutition, respiration, thermotactic, secretory, cardiac, and digestion.
In the medulla as in the spinal cord there are five main groups of cells.
First, the posterior or upper horns, from which come the somatic sensory
nerves. Second, Clark’s cells, located centrally, which are the origin of the
ganglionated splanchnic nerves. Third, cell groups of the lateral horns
which are the center for the non-ganglionated splanchnic nerves, and certain
other nerves for the viscera, including the enteric muscles. Fourth, cell

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groups of the anterior horns, which are the center of all somatic voluntary
muscles. Fifth, groups of single cells probably belonging to the posterior
horns which are probably centers for other splanchnic nerve fibers.

Fig. 77, A.

G, A section through the tuberculum bigeminum. 1, Pia mater. 2, Nerve fibers. 3,
Fine granular ground substance. 4, Thin layer of small cells. 5, Fine granular
ground substance. 6, A second thin cell layer. 7, Fine granular ground substance.
8, Third thin cell layer. 9, Fine granular ground substance. 10, Fourth widely
extended cell layer. 11, A fine granular layer. 12, A thick layer of spindle cells.
13, A layer of medullated nerve fibers. 14, Ependemal cells. 15, The sinus.

H, A transverse section through the medulla oblongata, 1, 3, 4 and 6 are
ganglionic centers. 2, The dorsal groove. 8, The ventral fissure. 5, The central
canal. 7, Fiber tracts.

I, A transverse section through the cervical portion of the spinal cord. 1, Ventral
septum. 2, Dorsal septum. 3, The central canal. 4, The dorsal horn. 5, The ventral
horn.

J, A section through the wall of the oil gland, or rump gland. 1, The stroma. 2,
The tubular glands some of which are branched.

K, A section through a spike of a comb of a cock. 1, The epithelial layer. 2, A
dense fibrous subepithelial layer. 3, A second fibrous vascular layer. 6, A denser
central core supporting the large arteries and veins. 4, A vein. 5, An artery.

L, A section through a lobe of the wattle of a hen. 1, The epithelial layer. 2, A
dense vascular layer. 3, A vein. 4, An artery. 5, A loose fibrous vascular structure.

Page 321

The gray matter in the cord is in the form of two commas placed with
their backs together with the central canal passing between them. The
central canal is located in the center of the cord. As the cord nears the
medulla oblongata the form of the gray matter changes. The second, the
third, and the fifth ganglion centers are arranged laterally, and show a
distinct side-horn group. The central canal separates the two Clark’s
columns; later the side-horn group enlarges and extends ventrally around
the anterior horn group and joins on the other side in half-moon shaped
formation.
The central ganglionic mass of the spinal cord, the center for the enteric
visceral system, is divided into three complex parts. First, there are cell
groups on both sides of the posterior raphe. Second, the half-moon shaped
ventral groups extending parallel peripherally described above. Third, lying
between groups one and two a complex group, which possesses a large
collection of cells. These furnish splanchnic nerve centers, the anterior
supplying motor nerves and carrying motor impulses outward, and the
superior sensory which carry impulses to the centers. The cell group of the
superior horns takes a sidewise peripheral position (Gadow).
The cerebellum (Fig. 62, C, 2) is located above the medulla oblongata
and posterior to the cerebrum. The cerebellum consists principally of a
median lobe called the worm. The lateral lobes are conical and rudimentary.
The under part of the worm forms the roof of the fourth ventricle.
On the upper surface of the cerebellum are numerous transverse
markings (in the hen 13 or 14) which divide the lobe into leaves. When the
cerebellum is cut lengthwise there is observed on the sectioned surface the
peculiar arrangement of the white and the gray matter, the arbor vitæ,
mentioned above. There is a small cavity in the cerebellum which
communicates with the fourth ventricle.
The cerebellar cortex shows four parts, namely: First, the central part
composed of white medullated fibers, between which are arranged
neuroglear cells. Second, a rather reddish layer of cells of different sizes.
These cells are embedded in a fine ground substance and are about 0.003
mm. in diameter. Third, a plain layer of large pear-shaped ganglion cells,
the cells of Purkinje. Fine branches extend outward from the apex of these
cells. Fourth, an outer gray layer which consists of small multipolar nerve
cells with some neuroglear cells. The color of these three layers, according

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to Gadow, depends upon the color of the plumage; that is, if the plumage is
dark, this layer is dark; if light, the layers are light. The marked coloring is
said to be most distinct in the second layer.
The anterior portion of the cerebellum consists of medullated nerves
whose fibers run crosswise. These are the extensions of the true cerebellar
fibers, which become fewer and fewer as they proceed anteriorly. Finally, a
few remaining fibers running crosswise fuse as the commissura Sylvii, and
extend into the lobi optici. A layer of nerve cells extends under these
medullated nerve fibers.
A bundle of fibers extending from the medulla oblongata. These fibers
extend into the optic lobes, form the crura cerebri, or peduncles of the
cerebri, and also form the inferior wall, or floor, of the aqueduct of Sylvius.
The crura are sometimes spoken of as the partes pedunculares. These
contain gray matter. The following division is made of the ganglion of this
region. First, a group of cells near the base of the peduncles, which are
divided from the ventral rim by the arciform fibers. This ganglionic
formation may be considered an extension from the medulla oblongata.
Second, a group of the ganglion cells of the lobus optici. Third, a group of
cells lying near the lobus opticus, which give rise to the ascending roots of
the trigeminus. Fourth, a group of ganglionic cells from which spring the
roots of the motores occuli, and which lies near the middle line and under
the sulcus centralis. Many ganglion cells are found to the right and to the
left of the sulcus centralis, which show different arrangement of the cells at
different levels. Fifth, a group of irregular cells which extends centrally on
the superior walls of the third ventricle and to the superior part of the lobus
opticus.
The microscopic structure of the roof of the lobus opticus, or corpus
bigeminum, shows that the layers are arranged parallel to the pia mater and
are divided into the following parts:
Externally, the pia mater.
An outer layer of very fine nerve fibers, which lies just below the pia
mater.
A layer of fine granular ground substance.
A thin layer of small cells the diameter of each of which is 0.038 mm.
A layer of fine granular ground substance.

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A second thin cell layer.
A zone of fine granular ground substance.
A third thin cell layer.
A fine granular ground substance.
A fourth widely extended cell layer.
A fine granular layer.
A somewhat thick layer of spindle-shaped cells.
A layer of medullated nerve fibers.
This last is the inner layer of nerve fiber. On the inner surface of this
layer we find the ependymal cells, the cells that line the cavity of the optic
lobes. The commissura Sylvii form the covering of the lobi optici and join
these two lobes. This commissure is formed from the upper and the lower
layer of nerve fibers. In the commissure these fibers cross each other.
The hypophysis (Fig. 62, No. C, 20) lies back of the chiasm, or optic
commissure, and below the middle of the third ventricle. The infundibulum,
a pedicle-like structure, connects the hypophysis with the third ventricle of
the cerebri. It contains a cavity and forms an extension of the third
ventricle. The hypophysis is divided into two lobes, an anterior and a
posterior.
The third ventricle communicates anteriorly with the lateral ventricles of
the cerebri through the foramen of Monro, and posteriorly with the fourth
ventricle through the aqueduct of Sylvius. The posterior walls of the third
ventricle are relatively thick and form the posterior brain commissure. The
wall is thin from the commissure to the chiasm. Within it lie two ridges,
which connect the two hemispheres with the corpus callosum, and, farther
anteriorly, with the anterior cerebral commissure. The space from the third
ventricle and to the anterior commissure is called the laminæ terminales.
The pineal gland, located between the cerebri and the cerebellum, lies
against the choroid plexus, which covers the highest point of the third
ventricle.
The cerebrum is divided by a deep longitudinal fissure into two
hemispheres. The cerebrum is shaped somewhat like the heart on a playing
card. The lower face is somewhat flattened. The upper and lateral sides are
not provided with convolutions or sulci, but are smooth. The fissure of

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Sylvius is faintly marked on the inferior face. The olfactory lobes appear
well developed and are relatively large for the size of the brain. They lie
close together on the extreme anterior portion in the median line.
The olfactory cerebral crura emerge from the cranium at the upper angle
between the posterior wall, the roof, and the septum of the orbit, and pass
through the olfactory foramina and in grooves on the upper part of the
septum; then passing forward they penetrate the frontal structure and are
finally distributed over the turbinated mucous membrane.
The corpus striatum is large; it occupies nearly the entire floor of the
ventricles.
The anterior commissure is found between the hemispheres. Its middle
part lies in the lamina terminalis on the division between the anterior and
the middle brain, and close to the thalami optici. Its side extensions are
rounded masses called the nervi amygdales.
The corpus callosum, quite rudimentary, lies on the posterior dorsal rim
of the anterior commissure.
The corpus striatum forms a thin broad ridge, which passes ventrally.
This structure consists of twenty-five large pyramidal cells which lie in the
posterior lateral dorsal section, and of from ten to fifteen pyramidal cells
which are located in the rest of the section. In addition to these two groups
there are many cells about 5 millimeters in diameter. These lie, six or more,
in a nest imbedded in neuroglia. There is a thin layer of spindle cells near
the ventral line. The outer nerve nest, or nerves amygdalis, lies in the
posterior lateral ventral part. It is covered by a thin membranous layer. Its
cells are pyramidal in shape and are from 10 to 15 millimeters in diameter.
The cells terminate in spindle form toward the periphery. Nerve fibers
extend from the anterior commissure.
The outer wall of the corpus striatum consists of the following layers:
An outer white layer consisting of fine medullated nerve fibers imbedded
in a ground substance containing numerous nerve cells.
A layer of ganglionic cells, consisting of pyramidal cells from 10 to 15
millimeters in diameter, of other round cells 20 millimeters in diameter, and
finally of cells only 5 millimeters in diameter. This layer forms a reddish
line in the dorsal portion of the corpus striatum.

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These layers form part of the median and the posterior cerebral wall of
the lateral ventricle. The lateral ventricle is closed except for a slit-like
opening behind the posterior commissure. This is the foramen of Monro,
through which the lateral ventricle communicates with the middle, or third,
ventricle.
The choroid plexus is found at the base of the lateral ventricle.
The wall of the lateral ventricle becomes thinner near the region of the
transverse commissure on the surface toward the middle brain. At this point
the pia mater and the ependyma, or the lining cells of the ventricular
membrane, form the major part of the wall.
The domestic fowl does not have the hippocampus.
The wall of the middle ventricle consists of an outer white layer, which is
arranged similarly to that of the corpus striatum. The ventral rim of the wall
is formed by a spiral band which consists of fine medullated fibers, in
which are imbedded a few cells.
The processus cerebri mammillares are also called the tubercula
olfactoria. From these structures extend forward the olfactory nerves, the
posterior roots of which may be traced to the walls of the lateral ventricles.
The structure of the processus cerebri mammillaris is made up of five
layers as follows:
An outer layer, which consists of colorless olfactory fibers extending in
all directions.
A granular ground substance layer, in which are imbedded a few cells.
A thicker granular layer, on the inner edge of which are twenty large
pyramidal cells with processes pointing outward.
A layer of closely packed cells, in which are fine medullated nerve fibers.
These cells are about 5 millimeters in diameter.
An innermost layer of ependymal cells.
Near the hemisphere the peripheral nerve fibers and nerve cells
disappear, leaving only the ground substance of the processus to aid in the
formation of the hemisphere.
There is a long bundle of fibers on the lower surface of the hemisphere,
which blends with the substance of the olfactory fibers.

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The peduncles of the cerebrum (Fig. 62, No. 21) are the slightly
diverging columns of nerve tissue, which form the anterior continuation of
the medulla oblongata and disappear under the optic tracts and the chiasm.

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THE SYMPATHETIC NERVOUS SYSTEM

The sympathetic nervous system commences anteriorly at the large
superior cervical nerve ganglion. This ganglion, anteriorly, brings into
communication the glosso-pharyngeal, the pneumogastric, or vagus, and the
sympathetic system.
The following nerve trunks emerge from the superior cervical nerve
ganglion: a large trunk fusing with the vagus and directed downward,
accompanying and surrounding the carotid artery; a second large trunk
fusing with the recurrent pharyngeus and the glosso-pharyngeus; a third
trunk which merges with the hypoglossal; finally several trunks which are
distributed to the head.
The temporo-lacrimalis, one of the large sympathetic nerves of the head,
as it extends from the cervical nerve ganglion, receives branches from the
ganglion radicis vagi. This nerve, passing between these two ganglions,
extends horizontally forward and outward through a foramen, crossing the
glosso-pharyngeus. Near the Fallopian canals it crosses the facial nerves,
lies supero-laterally, and receives a short branch from the facial nerve
whose fibers are traceable to the geniculate ganglion. It also receives a
branch from the recurrent maxillaris.
This nerve accompanies the external ophthalmic artery forming around it
a network of fibers, called the external ophthalmic plexus. It lies outside
and downward from the optic nerve, sends fine branches to the external
ophthalmic artery and to the masseter artery, and extends along with a small
branch of the superior maxillary nerve to the skin of the outside rim of the
eye cavity.
The ophthalmic plexus, a second trunk extending to the head, enters in its
course, anteriorly, the lacrimal plexus. Its fibers also supply the lacrimal
gland, and finally anastomose with the second recurrent branch of the
trigeminus.
The sympathetic caroticus cephalicus nerve, a third trunk extending to
the head, after emerging from the large superior cervical nerve ganglion,
receives some small branches from the glosso-pharyngeal ganglion, and
then enters, in a horizontal manner, a foramen, the canalis caroticus

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externus, located in the lower part of the basi-occipital and the sphenoid
bone. The anterior opening of this foramen, or canal, is close to the
posterior part of the pterygoid bone. Inside this canal the sympathetic
caroticus cephalicus receives a small branch which extends in a straight line
from the basal part of the facial nerve. After receiving this branch, the nerve
trunk, passing to the ear drum, lies close to the petrosum and the sphenoid.
It is covered by the masseter muscle. The carotic ganglion is located at the
point of the fusion of the caroticus cephalicus with the main trunk. At this
point the caroticus cephalicus divides into two branches. The first is the
superior recurrent nerve, which lies close to the upper surface of the alæ of
the sphenoid, passes between the obliquus externus and the orbital wall,
around the eyeball, and finally into the orbital septum and the internal
muscles of the eye. It communicates with the ophthalmic nerve and sends
twigs to the lacrimal gland, the gland of Harder, the upper eyelid, and the
nose. The orbito-nasale ganglion is located where these nerves
communicate near the nasal region. The second branch of the sympathetic
caroticus cephalicus is the inferior recurrent nerve. This branch passes
forward and dorsally from the pterygoid bone to a point where the upper
rim of the rising wings of the jaw bone meets the sphenoid rostrum. In this
course, some branches are given off to the pharynx, one branch near the
lacrimal gland, and a branch which communicates with the superior
maxillary nerve just before the nerve enters the jaw bone. The spheno-
palatine ganglion is at the point of fusion.
The terminal branches of the spheno-palatine are distributed to the hard
palate, the nose, and the lacrimal gland.
From the large cervical nerve ganglion and near the roots of the caroticus
cephalicus are given off a few small nerve fibers which pass alone to the
pharynx or accompany the jugular nerve branches, and fuse with the main
trunk of the caroticus cephalicus nerve.
From the large superior cervical nerve ganglion the sympathetic trunk
extends downward toward the thorax. It is covered deeply with muscles.
This portion is known as the cervical sympathetic nerve trunk. A trunk lies
on each side of the cervical vertebræ. The large thoracic nerve ganglion, the
inferior cervical, is located along this trunk at the entrance of the thorax.
From this ganglion there is given off the recurrent cardiacus which supplies
the heart. The end branches of the sympathetic nerve trunk blend with the

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pneumogastric nerve. The inferior nerve ganglion is the ganglion
cardiacum. Near this ganglion is found a nerve plexus in which there are
imbedded peripherlistic ganglia. This thoracic plexus, accompanying the
collica artery, passes to the abdominal region, supplying the intestines and
taking part in the formation of the abdominal plexus. The abdominal plexus
is located near the anterior portion of the kidneys. Its fibers are directed
mainly downward to the visceral organs. The large intestine, the rectum and
the copulatory organs receive branches. These latter branches take part in
the formation of the pedunda nerve plexus. Some branches of this plexus,
follow the branches of the posterior mesenteric artery.
The thoracic trunk (Fig. 64, No. 42) of the sympathetic is double. The
anterior portion gives off an anterior splanchnic nerve, or plexus (Fig. 64,
No. 43) which accompanies the celiac axial artery to the gizzard and liver,
communicating with the pneumogastric. The posterior splanchnic nerve is
intimately combined with the adrenal body, and the testes, or the ovary (Fig.
64, No. 45). Intestinal branches accompany those of the mesenteric arteries
(Fig. 64, No. 46). Other branches supply the kidneys, and communicate
with long branches of the spinal nerves destined for the cloaca and adjacent
parts, and thus form a plexus similar to that found in mammals.

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FUNCTIONS OF THE NERVOUS SYSTEM

According to function, the nerves composing the trunks are divided into
afferent and efferent.
The afferent nerves are those that convey the impulses from the periphery
of the body to the nerve center, which are located in the brain or in the
spinal cord. The impulses conveyed are those of special senses, as sight,
hearing, taste, touch, and smell. Impulses producing sensation pleasurable
or painful come from the skin, the muscle, or the viscera.
The efferent nerves are those which convey impulses from the nerve
centers to the periphery. These impulses may be motor as those going to the
muscle cells of the skeletal muscles, the viscera, or the blood-vessels. These
motor impulses make movements in these organs possible. In the blood-
vessel they result in the control of the caliber of the vessel. These impulses
may be of an inhibitory character, as in slowing the heart. They may be
secretory impulses stimulating the gland to activity or regulating
metabolism.
The ganglia are nerve centers which receive and generate impulses; the
nerve trunks are filaments which convey impulses. The gray matter of the
cord described above is the ganglionic portion, and the outer white matter is
made up of nerve fibers which convey impulses from one part of the cord to
another, or to and from the brain.
The nerves that have their roots in the spinal cord superiorly, are sensory;
that is, they convey the sensory impulses from the periphery to the cord
ganglion and to the brain. They have a ganglion just outside the cord.
The nerves that have their roots in the spinal cord inferiorly; that is, they
convey motor impulses from the nerve centers to the periphery. The
function of the inferior roots is to supply all the voluntary muscles as well
as the oviduct, the intestines, and other hollow viscera, including the blood-
vessels with the power of movement. Many of these fibers pass to the
sympathetic ganglion and are distributed as sympathetic nerve fibers.
The cord is divided into different tracts, that is, certain groups of fibers
convey certain kinds of impulses.

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The superior column of the cord conveys to the cerebrum such
impressions as temperature, pressure, and muscular tension.
The fibers of the lateral columns carry sensations of pain.
The fibers of the direct cerebellar tract carry impulses which result in the
maintenance of the equilibrium of the body.
All the voluntary impulses originate in the cerebrum, pass through the
cerebellum and travel direct to the bulb; they then pass over to the opposite
side, and travel by the crossed pyramidal tract to the multipolar cells of the
inferior horn of the spinal cord, and transmit the impulse through motor
fibers that originate at that point in the cord.
All sensory impulses enter the brain on the side opposite their origin, and
all motor impulses leave the brain on the side opposite that to which they
are distributed. Injury of the motor area of the right side of the brain leads
to paralysis of the left side of the body.
An impulse of the vasomotor nerve travels in the lateral column of the
cord.
A nerve impulse may originate in the brain and be modified in passing
through a ganglion in the spinal cord or in the sympathetic system.
The system of reflex action is as follows: first, an efferent nerve which
conveys the impulse from the periphery to a nerve center; second, a
ganglion, or nerve center, to receive the impulse and generate other
impulses; third, an efferent nerve to convey the impulse from the nerve
center to the periphery.
The following is an example of reflex action. The foot of a fowl is
pierced with a pin. The sensory impulse is conveyed by sensory nerve fibers
to the nerve centers. In this center the ganglionic nerve cells generate a
motor impulse which is sent back through the motor nerve fiber to the
muscles controlling the part. The result is that the muscle contracts and
jerks the foot.
There are many functional centers located in the medulla oblongata.
Destruction of this part of the system results in instant death of the bird. In
addition to furnishing a path for fibers carrying impulses from the body to
the cerebrum, it furnishes a large number of centers for such functions as
respiration, swallowing, secretion, temperature, and vasomotor and cardiac
activity.

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The function of the cerebellum is principally that of coördination. It
brings about harmony and rhythm in muscular movements. If the
cerebellum be removed, the bird can no longer walk. It has lost, with this
removal, all power to coördinate.
The cerebrum of the bird has no convolutions, and the gray, or
ganglionic, portion is thin, indicating low power of intelligence. There are
certain areas presiding over other functions, as motor areas, sensory areas,
and so on.
A careful study of the brain of the fowl shows us that the centers
presiding over sight and smell are well developed.
The olfactory bulbs are the centers of the sense of smell.
The optic thalamus is the center of the sense of sight.
The sympathetic nerve system transmits impulses to the involuntary
muscular structure of all organs, including those of the intestinal tract, the
blood-vessels, and perhaps also the glands.

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ESTHESIOLOGY

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THE SENSE ORGANS

The five special senses are seeing, smelling, tasting, hearing, and feeling.

THE ORGAN OF SIGHT

The sense of sight in the bird is well developed. The eye (Fig. 26, D, E
and F), the organ of sight, is relatively large, round laterally, and rather
flattened antero-posteriorly. It is located at the side of the head. The eyeball
is only slightly movable. The septum interorbital separates the two eyeballs
laterally. As in mammals, the eyeball has three coats, which are from inside
to outside, the retina, the choroid, and the sclera. The sclerotic coat is
completed anteriorly by the cornea with which it forms a union called the
corneo-scleral juncture. Around the cornea the sclerotic coat contains a ring
of osseous scales varying in number from twelve to twenty. The sclera may
become ossified posteriorly, forming an osseous sheath around the optic
nerve. The pecten is a vascular comb-like membrane stretching from the
nervous opticus to the crystalline lens. The choroid coat is always black.
The pupil in the hen is also black and round. The iris contains striated
muscular fibers. The membrana nictitans, located at the inner angle is well
developed. It is moved by two muscles (Fig. 26, No. B, 7, 8, 10). The
lacrimal gland and the gland of Harder are present. There is no meibomian
gland.
The tears are secreted by the lacrimal gland and are drained away from
the fore part of the eyeball by two small canals which extend into a lacrimal
sac. From this sac there extends a tube into the nasal cavity called the
lacrimal duct.
The lower lid is the larger and often incloses a small cartilaginous plate.
The conjunctiva is a true mucous membrane which covers the anterior
portion of the eye cavity attaching to the cornea-scleral juncture.
The choroidea is rich in pigment. On its inner surface lies the dark
pigment layer of the retina. The corpus ciliare, that part of the choroid coat

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bearing the ciliary processes, consist of numerous folds. The ciliary muscles
are arranged obliquely. Each consists of three digitations.
The iris is covered on the posterior side with pigment, the color of which
determines the color of the eye. The yellow pigment of the iris has been
said to be due to carotin and xanthophyll and the black pigment to melanin.
The enlarging and the contracting of the pupil is brought about by muscles.
The reduction of the pupillary caliber is due to the sphincter pupillary
muscle. It is said by some anatomists that the muscles controlling the
caliber of the pupil in the bird furnish voluntary motion and that the
capability of accommodation of the eyes is greater in birds than in
mammals.
The retina contains no blood-vessels; otherwise the structure is similar to
that of mammals. The crystalline lens is flattened on the corneal side and is
convex posteriorly. The lens epithelium develops into fibers in the parts
close to the equator, and are almost perpendicular to the eye axis. The
corneal portion is relatively small.
The sclerotic coat is dense and white. It is divided into three layers. It is
thin and flexible, and somewhat elastic posteriorly. It has an internal layer
of hyaline cartilage. Anteriorly its form is maintained by the circle of
osseous plates mentioned above. These plates, interposed between the
exterior and the middle layer, are located immediately behind the cornea.
The scales are thin and of oblong quadrate shape, being elongated from
before backward.
The choroid coat is a membrane loosely cellular and highly vascular. It is
impregnated by a black pigment. Opposite the bony circle the choroid
separates into two layers. The external layer is the thinner and adheres at
first firmly to the sclerotic; it passes forward to become continuous with the
iris. The inner layer is thicker than the external. The two layers are made up
of radiating fibers which terminate anteriorly in the ciliary processes, the
ends of which are adherent to the capsule of the crystalline lens.
The iris is delicate in structure. It is composed of a fine network of
interlacing fibers.
The ciliary nerves and blood-vessels run in the form of single trunks
between the choroid and the sclerotic, and terminate anteriorly in a ring-
shaped plexus for the supply of the iris and the muscular circle of the

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cornea. As stated before, the pupil in the fowl is round, but in the goose it is
elongate transversely; and in the owl, a vertical oval.
The optic nerve approaching the sclerotic coat becomes altered into a
conical extremity, which enters a sheath and is directed downward and
obliquely forward. The extremity of the optic nerve in the interior of the eye
presents a white narrow streak. Branches of the opthalmic artery enter the
eye between the lamina of the retina, along the whole extent of the oblique
slit, and penetrate the fold of the pecten upon which they form a delicate
ramification.
The crystalline lens is of soft texture. It is inclosed in a capsule and is
nearly round. It adheres very firmly in the depression in the anterior part of
the vitreous humor. The capsule is lodged between two layers of hyaloidea,
which as they recede from each other, leave around its circumference the
sacculated canal of Petit.
The cornea is of horny consistency and is transparent. Light thus rapidly
passes through it to the posterior part of the eye.
The vitreous chamber, lying back of the crystalline lens, contains a clear
jelly-like substance.

THE ORGAN OF HEARING

The ear, the organ of hearing, has in the fowl no conchal cartilage. The
external auditory meatus, or canal opening, is found on each side of the
head, and is usually guarded by a few stiff, short feathers. In some kinds of
birds these feathers are capable of being erected so as to direct the waves of
sound into the inner ear. The outer entrance of the ear contains glands. This
canal is short. It leads to the drum, which is somewhat convex from the
outside, and which has a membrane forming a complete curtain stretched
over the outer part. The irregularly formed drum has connection with the
air-containing cavity of the skull, and by a thin cartilaginous canal, the
Eustachian tube, with the pharynx. The auditory ossicles are represented by
only a single bone, called the columella, which most closely represents the
stapes of mammals. This is attached by processes of cartilage to the
tympanic membrane. Owen considers these cartilages as representing the
malleus of mammals. Huxley on the other hand considers them to represent

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the incus. Originating from the processes is a small muscle which is
attached to the drum. This is by Shufeldt considered the Tensor tympani.
The drum cavity through the fenestra vestibularis and cochlearis is
connected with the labyrinth.
The inner ear consists of a membranous labyrinth, surrounded by a
spongy bony structure—the bony labyrinth. In it are recognized the
vestibulum, the three half-circle shaped canals, and the cochlea. The
superior semicircular canal is the largest. The acoustic nerve enters at the
end of the canals near the ampullæ. The nerves are supported in delicate
vascular membranes lining the canals and slightly projecting into the
ampullæ.

Fig. 78.—Diagram of the inner ear. 1,
The integument. 2, The superior
semicircular canal. 3, The external
canal. 4, The horizontal canal. 5, The
ampulla. 6, The obtuse osseous conical
cochlear cavity. 7, The Eustachian tube.
8, The tympanum. 9, Filaments of the
auditory nerve.

The vestibulum is a small irregular cavity which communicates with the
arcades and the cochlea, and through the fenestra vestibularis with the drum
cavity. The endolymph of the vestibulum contains microscopic crystals of
calcium carbonate. The semicircular canals are relatively larger and thicker
than in mammals. The ampullæ in the upper and back part are separated by
walls. The cochlea is an obtuse conical tube-like structure slightly curved at
the blind extremity with the concavity directed backward. It contains a

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membranous lining. At this point the cochlea is broadened and
accommodates a branch of the auditory nerve. This nerve spreads out in
fine filaments upon the surface of the tubes. The hollow space of the
cochlea is divided by a spiral partition, making two chambers, the scala
vestibuli and the scala tympani. These walls extend from the beginning of
the cochlea.
The tympanic cavity is formed by the occipital, the basi- and
alisphenoids, the petrosal portion of the temporal bone. It represents the
stapedial canal leading to the foramen ovalis and the pneumatic apertures
by which the air from the Eustachian tube is conducted to the precranial
diploë.

THE ORGAN OF SMELL

The nose is the seat of the peripheral portion of the organ of the sense of
smell. The terminals of the olfactory nerves, which receive the impressions
of odors, are broadened in the mucous membrane of the walls of the
anterior nares. There are no ethmoidal volutes, or sieve-like structure, in
birds. The nerve extends from the anterior portion of the brain in cone-
shape, finally dividing into filaments which are distributed over the mucous
surface of the turbinated bones.

THE ORGAN OF TASTE

The most important part of the organ of taste is the tongue. In birds the
dorsum of the tongue is covered by a thick stratum corneum, a heavy layer
of stratified squamous epithelium. The tongue, therefore is not in birds so
well adapted for the perception of taste as it is in mammals. The lingual
branch of the trigemini is lacking in birds. This fact makes the ninth pair, or
the nervi glosso-pharyngei, the exclusive nerves of taste. There is an
opinion ventured by one anatomist that, since the first and the second
branch of the fifth pair, or trigemini, have terminal filaments in the hard
palate, they may furnish fibers for the sense of taste. There are many taste
cells on the tongue and on the dorsal palate.

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THE ORGAN OF TOUCH

The peripheral parts of the organ of touch in the fowl are the skin and the
feathers.
In a few birds special touch and taste perception can be supplied by the
edge and point of the beak.
In the skin of birds are found numerous sensory nerve endings for tactile
sense.
The sensory nerves, which provide the sense of touch, usually terminate
in one of two forms. The first are the Herbst’s bodies, which in many
respects are similar to the Picinian bodies.
Herbst’s touch corpuscles are found on all parts of the skin; they are
especially numerous in the region of the tail and of the wing. In the wing
they are particularly numerous in the region of the flight feathers. They
occur in large numbers in the periosteum of the anterior tibial region and in
the mucous membrane of the cloaca and of the generative organs. They are
numerous in the conjunctiva and on the surface of the tongue. They are also
found in the gums and in the beak.
Herbst’s corpuscle is made up of a central fiber-shaped part with a
smooth extension of the axis cylinder of its nerve (Fig. 29, G). This central
fiber is surrounded by a peculiar protoplasmic body. Outside of this there is
a double row of cubical cells which surround the axial part. These are close
together. Outside of these there occurs a concentric lamellar layer, which
contains cells. In the periphery these lamellæ become more distinct and
contain larger but fewer cells. The capsule is made up of very thin layers,
which are continued into the perineural layer. Each body contains a thin
outer zone. The nerve fiber passes in a regular manner from the axis
cylinder, the myelemma, and the sheath of Schwann, and as a delicate nerve
twig is surrounded by a sheath consisting of several perineural layers. As it
enters the center of the touch corpuscle, it loses its myeline sheath near the
base of the body, and the terminal fiber becomes flattened. Its rim is
directed toward the two rows of cubical cells, and it ends in a rounded
knob.
The touch corpuscles are the largest in the mucous membrane of the
cloaca and smallest in the skin. Hess has found these touch corpuscles in
the large filiform papillæ on the side of the tongue and a few on its lower

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surface. They are also found in the soft skin of the edges and inner borders
of the beak.

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STRUCTURE OF APPENDAGES

The skin of the fowl is very thin and does not contain oil glands or sweat
glands. In the fowl the oil is supplied by a tail or rump gland, the glandula
uropygii (Fig. 35, No. 16). This gland is round or oval in shape, and about
the size of a pea and consists of two lobes. It is of the tubular variety with a
teat, which, in most instances has two openings. A medium septum divides
the gland into two halves. The oil secreted by the columnar epithelial cells
is collected in a body cavity located in the center of the gland; this has a
duct extending to the surface. The bird by squeezing out a quantity of this
oil into its beak oils the feathers, passing the beak over them, one by one.
The oil renders the feathers practically impervious to water. It is necessary
for the bird to give proper attention to its plumage in order that the feathers
appear in prime condition. Should there be a disease of the oil gland, or
should the bird become ill and neglect its toilet the result is an unkempt
appearance of the plumage, the feathers becoming rather rough and more or
less injured by the weather.
The subcutis is well developed and furnishes to the cutis great capability
for movement, which is necessary for the rising and falling of the feathers.
The corneum is very thin. Papillary bodies are present only in a very few
places, such as the region about the eye and on the toes. Where the toes
touch the ground in walking there are large wart-like thickenings of the
epithelium. In most birds the shanks are unfeathered. The epidermis on the
feathered parts of the skin is thin, dry on the surface, and abounds in
continuous scales. The stratum corneum is very thick on the horny sheath of
the beak, on the top of the toes, on the spurs of the cock, and on the scale
plates that cover the skin on the shanks. The feathers of birds serve the
same protective purpose as hair on mammals. In cold weather the skin
muscles controlling the feather movements contract; thus the feathers

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become ruffled much as we observe the hair standing erect on horses under
similar conditions. By increasing the dead air space around the body, the
radiation of heat is retarded, and the body kept warmer. The corneum of the
skin is not usually rich in blood-vessels; however, in the domestic fowls
there is in the comb, in the wattles, and similar appendages of the head, a
thick vascular network.
The beak and the claws are modified skin; they are true horn material. At
the base of the beak there is often formed scales, which surround the
nostrils, in whole or in part, and have a naked, or waxy, appearance, which
is known as the cera.

Fig. 79.—Photomicrograph of the
section of skin from the sole of the foot
of a hen. 1, Horny stratified squamous
epithelium. a, Stratum corneum. b,
Stratum lucidum. c, Stratum
germinativum. 2, Connective tissue
supporting membrane, pars reticularis.
3, Blood-vessels.

The feathers may be considered of two chief kinds, the quill feathers and
the clothing feathers. The most rudimentary of the latter are known as
down. A quill feather consists of two principal parts: the quill, or calamus,
and the vane, or vexillum. The quill is continuous with the central shaft,
called the rachis, the two forming the stem of the feather. Projecting
outward from the stem on each side are a large number of pointed and very
flexible barbs. These barbs are located nearly at right angles to the quill and
have extending from them at right angles smaller processes or barbules.
These barbules hook together the barbs and give the web its form. In some

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feathers, as the hackle, and in the wing bar feathers of the male of some
breeds, there is a portion of the upper outer edge of the feather not provided
with barbules, which fact gives the feather its characteristic appearance. The
down feathers are loose and fluffy. In this kind of feather the shaft is weak,
and the barbs are not provided with barbules. The barbs like the shaft may
be considered weak. These feathers give great warmth to the body. There
are fiber feathers appearing as hair-like filaments, and called filo-plumæ.
These are found scattered over the body; they are particularly abundant in
the region of the head and the neck.
At each end of the quill is a small opening, or umbilicus. Inside the barrel
of the feather there is pulp, which in young feathers is very vascular; the
vessels entering by the proximal umbilicus are buried, along with part of the
quill, in a papillated follicle of the skin. From this follicle the feather is
developed. At the base of the shaft a secondary rudimentary quill is usually
formed, which may be represented by a mere tuft of down. On the same
general principle the smaller feathers are constructed. These cover the body,
the upper parts of the legs, and the head, while the larger feathers and quills
are confined to the wings and the tail. The longest quill feathers are those
arising from the hand, called the primaries. Those arising from the forearm
are called the secondaries. Those that are developed from the proximal part
of the arm are called the tertiaries. The rudimentary pollux carries some
feathers which form the alula, or bastard wing. The scapularies are feathers
covering the scapula and the humerus. Covering the bases of the larger
flight feathers are wing coverts consisting of several rows of small feathers.
The quill feathers of the tail are called the rectrices. The rectrices have
considerable mobility; their bases are covered by a row of tail coverts.
The pedal digits of the natatores are joined by a membrane, covered with
scaly skin, which forms the web foot.
The feathers in many parts of the body are developed in rows, there being
intervals, or elongated skin areas, between these groups of several rows,
which are not provided with feather papillæ, but which are covered over by
the feathers developed in front of these spaces. The definite feather lines, or
areas, have been called pterylæ. The intervening tracts devoid of feathers
are called the apteria.
The first outer covering of the bird, or baby chick, is a temporary one
consisting of fasciculi of long filaments of down. These fasciculi on their

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first appearance, are enveloped in a sheath, which soon becomes ruptured
and are entirely cast off by the time the baby chicks are ready to be taken
from the nest or the incubator.

Fig. 80.—Photomicrograph of the skin
of the neck of a S. C. White Leghorn
hen. 1, The skin possessing an outer
stratum, the stratum corneum, next the
stratum lucidum, next the stratum
granulosum and underneath the stratum
germinativum. Beneath the outer dark
band representing the upper skin strata
is the pars reticularis of the derma. 2,
Papilla showing from inside to outside
the hyaline feather wall, the stratum
corneum, the Malpighian layer of the
follicle, the corium. Inside the feather is
noted the pulp-like material.

The down fasciculi, each emerging from its small quill, are succeeded by
the feathers, which they apparently guide through the skin.
Feathers do not spring from all parts of the body alike; especially devoid
of feathers are those parts where chafing and friction is greatest, as under
the wings and in the groin.
At the end of the quill there is a small opening, the inferior umbilicus,
into which projects a papilla of the dermis. Where the quill emerges from
the skin there is another small opening, the superior umbilicus, from which
springs frequently a small feather called the hyporachis. The shaft, or
rachis, has a groove extending along that surface which lies next the body.

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In the newly formed chick the first indication of feathers is the formation
of papillæ, which is constituted by the upward growth of the dermis, or the
sensitive and vascular parts of the skin. Then the skin immediately around
the papilla sinks downward, so that later the papilla is inclosed in a follicle
of the skin. The epidermis over the papilla is the same as over the rest of the
surface. The horny outer layer of the epidermis forms for the growing
feather a protective sheath which is cast off as the feather is formed. The
feather proper develops from the underlying germinative layer, which as the
feather develops, forms a cylinder of cells. The lower part of the cylinder is
in touch with the papilla; this later becomes the quill (Fig. 80, No. 2). The
upper part of the cylinder develops the web portion of the feather. As soon
as the feather is fully developed the papilla, which has projected into the
quill and nourished it, is withdrawn, and the quill becomes filled with a
pithlike material forming septa, which extend in different directions.
Once a year, usually in the late summer or in the fall, the entire feather
coat is changed. This process is called molting. During this time the bird
appears in a somewhat depressed condition, the hen almost always ceases
laying. Birds also molt in the spring, to a limited extent. The male at this
time takes on the so-called breeding plumage, which is the most beautiful of
the year. It has recently been established by Rice, that the young fowl, in
reaching a stage of egg production, molts five times before the laying
period begins.
The structure of the skin of fowls is similar to that of the skin of
mammals. The skin consists of two layers the outer portion, or epidermis,
and the inner true skin, the cutis, corium, or dermis. If we study a section of
skin from the shank region of a fowl we find the outer portion is
differentiated into two distinct regions, the rete Malpighii and the stratum
corneum. The stratum corneum is the outer horny layer. The cells making
up this portion are fusiform, flattened, and in regular rows. The nuclei in
these layers of cells are not pronouncedly visible, and the outline of the
cells not clear in a section such as used in our ordinary methods of study.
The corneum is a compact mass of remnant cells which have lost the
appearance and their texture of living cells. It thus becomes modified into
scales upon the skin surface.
Between the stratum corneum and the stratum Malpighii there is another
zone which consists of the cells undergoing a transitional stage from a

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cubical shape to a more flattened appearance, and gradually becoming more
granular and hyaline.
The various parts of the epidermis are in close genetic relationship to one
another. The upper layer of epithelium is constantly being desquamated.
This casting off is compensated for by a continuous upward pushing of its
lower elements. Cell proliferation occurs in the basal cells and in adjacent
cellular strata of the stratum germinativum, or stratum Malpighii, where the
elements are often seen in process of mitosis, or cell division. The young
cells are gradually pushed upward. During their course they assume the
general characteristics of the elements composing the layers through which
they pass. This process is as follows: each cell changes first into a cell of
the stratum Malpighii; then, when it commences the formation of
keratohyalin, it changes into a cell of the stratum granulosum; later still,
into a cell of the stratum lucidum; and finally into an element of the stratum
corneum, where it gradually loses its nucleus, cornifies, and at last drops
off.
The mesodermic portion of the skin consists of loose, subcutaneous
connective tissue containing some fat. The amount of adipose tissue in the
subcutaneous layer is subject to great variation; there are a few places in
which there is little or no fat. The upper portion of this layer contains a few
elastic fibers, which interlace and run in all directions. Numerous round or
oval cells are found in the upper region. The lower and middle portions of
the corium are richly supplied with blood-vessels terminating into
capillaries, which penetrate the portions bordering the epidermis. Nerves
giving off terminal branches also occur.
The various colors of the skins of fowls are due to the distribution of
various quantities of two colors, orange-yellow and brownish-black.
The yellow pigment is probably carotin and xanthophyll, two pigments
contained in association with the chlorophyll of plants, which the bird
obtains in its feed. These coloring matters were formerly called lipochrome;
but as lipochrome may be any coloring matter of fat, it is not sufficiently
definite. This yellow pigment, when present, is diffused through all parts of
the cell. When dilute, it gives a yellow hue; when concentrated, orange. It is
found in the epidermis and in the fatty masses of and beneath the corium,
and is probably identical with the yellow color of fat in other portions of the
body and in the yolk of the egg. A yellow shank, in a heavily laying hen,

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soon loses a part of its pigment; this is also noted of the coloring matter in
other parts of the body. This fact indicates that the coloring matter of the
fatty part of the egg yolk is from the same source as that of the fat. The
draught of this substance is more than normally and the reserve is being
drawn upon. Feed rich in zanthophyll and carotin cause intense yellow
colored yolks, and feeds poor in these substances cause the yolks to be a
pale yellow. Cotton seed meal contains two pigments, one a yellow
crystalline substance and the other a brownish resinous substance. Both of
these pigments are probably deposited in the egg yolk. The eggs of some
hens contain a large quantity giving a light brownish-yellow color to the
yolk.
The brown or black-brown pigment is carried in microscopic pigment
granules, which may be scattered through the ordinary cells or may be
confined to special pigment cells. The former are confined to the epidermis;
the latter may be found in both layers, but infrequently in the epidermis.
When granules are present in the flattened cells of the corium, they occupy
the nuclear region. They lie in short thin lines while those of the under
portion of the Malpighian layer occur in oval groups. Where these granules
occur in the rete layer, they cluster around the nuclei. In the colored skin
there are dark pigment granules found in the corium and to a less extent in
the rete layer. Hanau has described a definite cellular body which he found
densely packed among the black-brown granules. There is a central body
which sends out branches in all directions. In very dark skinned shanks
these ramifying strands interlace, and form a compact network, which in
many cases is so thick as to give the impression of a homogeneous mass.
Here and there occur round or oval pigmented bodies, which Hanau
concluded were the star-shaped cells with their pseudopod-like appendages
contracted. Pigment cells commonly lie around blood-vessels, clearly
indicating their course. They frequently form a compact tube, but more
often are limited to fragments which only partly enclose the vessels.
Pigment cells occur in several well-defined localities: in the upper portion
of the cutis among the closely interwoven strands of connective tissue; in
the region bordering the blood-vessels; in proximity to nerves, in nerve
endings and in surrounding fat masses. Isolated granules are frequently
scattered throughout the lower section of the corium. Barrows concludes
that the lower bodies of pigment play little or no part in the color of the
external shank, as they lie far below the opaque connective tissue. Melanin

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pigment granules are always contained in the pigment cells. When found in
the Malpighian layer, the pigment cells are of an oval form.
Immediately below the epidermis in the shank skin, extends a space less
in width than the row of columnar cells, which is devoid of pigment. The
brown pigment is melanin, which in large quantities takes on a black hue.
White skin does not contain superficial pigment. Melanin has been
observed in the study of white shank skin, but it lay at considerable depth or
in quantities insufficient to be noticeable. In some breeds of fowls, as the
Mottled Houdan, there are areas in which much melanin is irregularly
deposited, which circumstance gives the leg its mottled appearance.
The yellow color is the result of a deposit of the yellow pigment in the fat
of the shank. This may be deposited in both layers of the skin, or in the
corium alone. When present it is diffused throughout the entire cell as well
as throughout the intercellular substance. In young birds the Malpighian
layer contains much yellow pigment. Old hens have only small quantities in
the corneum. In breeds with normal yellow shanks old hens that have never
laid eggs show a deep orange color in both the dermis and epidermis.
In blue shanked birds melanin is present only in the corium. The black
pigment is seen through the semi-transparent Malpighian stratum, making it
appear bluish instead of brown or black.
The black shank color results when melanin appears in the epidermis.
Two forms of black pigment occur in the epidermis: granules in both layers
and pigment cells in the rete Malpighii.
The green shank is produced where there is pigment in the epidermis and
numerous melanin pigment cells in the upper corium. It is an optical effect
due to melanin lying under the semi-transparent yellow epidermis. There is
no melanin in the epidermis.
In the beak the corium of the skin is represented by a thin layer located
between the periosteum and the stratum Malpighii. Numerous blood-
vessels pass into it, and in the soft horn-like skin, occur sensory nerve
fibers.
The nails originate from the epidermis, of which they are a modification.
The nails of the toes are bent downward. They present a convex dorsal
surface and are concave ventrally. The dorsal surface consists of a horny
plate, which is set in a nail matrix. The ventral portion merges with the

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sides of the upper half, and, as the lower portion is the softer and wears
faster, the nail has a sharp point and edge. The matrix is formed by a growth
of the Malpighian layer of the cutis. A fold of skin lies over its posterior
part. The epidermic cells of the dorsal, or nail, part, and the base of the
ventral part grow fast. The outer cell layer gradually becomes horn-like.
The spurs are conical with a flat base. The basal part rests upon an
enlargement of the shank bone. Soft structure is found between the horny
spur and the bone. The upper cells, like those of the nails and of the skin,
are constantly being worn or cast off, and new cells push up from the lower
layers of cells. These newly formed flattened cells soon become cornified.
The oldest formation is found at the tip and the youngest at the base.

Page 350

EMBRYOLOGY OF THE CHICK

That a new individual may be brought into existence, there must be
accomplished the union of the male element, or spermatozoon, with the
female element, the ovum. This union is called fertilization. In the fowl this
fertilization is accomplished at the anterior portion of the oviduct, after the
calyx has ruptured and discharged its yolk, and before the albumen has been
formed around it. The blastoderm is found on the surface of the yolk. One
spermatozoon is all that is required; in fact, only one can be used in this
union.
Spermatogenesis.—The spermatozoa are formed by the seminiferous
tubules of the testis. From these cells, called the spermatogonia, are formed
other cells called spermatocytes, which in turn form the spermatids, the
immediate forerunners of the spermatozoa. During the period of
multiplication the spermatogonia divide repeatedly by mitosis. Numbers of
small cells are thus produced, each containing in its nucleus the number of
chromosomes typical of the somatic cell of that fowl. In the second period
the cells become larger and spermatocytes of the first order are formed.
Then comes the period of maturation, during which two succeeding
divisions rapidly occur. The first division results in the formation of two
cells exactly alike. These are spermatocytes of the second order. They differ
from the somatic cells in that they contain only one-half the typical number
of chromosomes. The second division produces two similar spermatids
from one spermatocyte of the second order. Therefore four spermatids
exactly alike may be formed from one spermatocyte of the first order. From
these spermatids the spermatozoa are formed (Fig. 55). The heads of the
spermatozoa contain the nuclei derived from the spermatids; the necks
contain the centrosomes; and the tail, consisting of three parts is probably
formed from the protoplasm. Three parts of the tail are as follows: first, the

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pars conjunctionis, which unites the tail to the neck; second, the pars
principalis, which constitutes the main length of the tail; and, third, the pars
terminalis, which consists of an axial filament which transverses the entire
tail and is surrounded by a protoplasmic sheath.
Oögenesis.—The ovum during its formation passes through three stages.

Fig. 81.—Section of ovum in a hen. 1.
Nucleolus. 2. Nucleus. 3. Liquor
folliculi. 4. Stratum granulosum. 5.
Follicular cells. 6. Theca folliculi. 7.
Peripheral stroma.

The first stage, that of division, takes place before the chick is hatched,
and, according to Bradley, comes to an end about the time of hatching. This
stage consists of the rapid formation of ova in the female chick. In the
second stage, which begins about the time of hatching, there is an increase
in the size of the units of the ovary, accompanied by yolk formation. At this
time each ovum is in its own follicle (Fig. 81), and is surrounded by a layer
of cuboidal cells and a theca. The theca is formed from the adjacent fibrous
stroma. The third stage, that of maturation, commences during the
development of the yolk and is complete after it has escaped to the oviduct.
Maturation consists of each cell’s dividing into two unequal parts. In each
division the cell is split into a small cell known as the polar body, which is
cast off and disappears, and a larger cell, which is the ovum proper. In this
process half of the original chromosomes are cast off.

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Fertilization.—The sperm travels rapidly; experiments have shown eggs
to be fertile laid twenty-four hours after service by a male. When the ovum
is discharged into the ovarian pocket it is surrounded by spermatozoa.
After the male pronucleus has united with the female pronucleus in the
single-celled ovum, there is a cleavage of the cell in the long axis of the
egg, making two cells; and then a cleavage at right angles, which
progressively continues, makes the mulberry-like mass. The remaining
content of the egg consists of food for the development of the embryo.
From this mass of cells before the egg is laid the blastoderm is formed. The
cells of the blastoderm are differentiated into two layers. The superficial
layer is the ectoderm and the lower layer is the entoderm. In the newly laid
egg the blastoderm may be observed. It is about 4 millimeters in diameter. It
has a transparent central area, the zona pellucida, which is located over the
subgerminal region. There is a peripheral, less transparent area called the
zona opaca.
In the fertile egg, as soon as it is subjected to the proper temperature, cell
multiplication in the blastoderm begins. The first signs of such change are
noted in the pellucid area of the blastoderm where embryonal traces appear
in the form of the parallel lines called the plicæ primitivæ, which diverge to
form the cephalic dilatation. At about this time takes place the formation of
the myelencephalous columns, in which the blood lakes expand in the
surrounding halones and in the tracts along which pass colorless blood
particles. These tracts extend from below the cephalic expansion to the
peripheral sinuses, as the proto-vertebræ, which begin to appear at the sides
of the myelon. The red color is acquired by the blood, and the heart by its
movements, is made more manifest as the punctum saliens. A distinct
membrane, the serous layer, is formed upon the germ and the blastoderm.
The cephalic end of the embryo rises from the surface of the blastoderm,
and then, curving down, sinks into it, forming for itself a kind of hood of
the serous layer. This hood gradually extends from the margin of the fossa
over the body, and, meeting a similar fold formed by the projecting and
incurved tail, closes over the germ on the upper side, making a
circumscribed cavity, which is the amnion. The progress of differentiation
of layers of the blastoderm has, meantime, gone on beneath. The serous
layer is in part reflected from the vascular and from the mucous layer. The
mucous layer is concerned in the formation of the intestinal canal; and
beyond this part, which is at first an open groove, the mucous layer expands

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over the yolk, which it ultimately incloses, the margins of the vitellicle so
formed contracting and uniting at the side opposite the embryo at a sort of
cicatrix, to which the last part of the abdominal yolk adheres. The vitellicle
is richly vascular, and the surface next to the yolk is augmented by rugæ.
The fowl’s egg, at about the fortieth hour, shows the buds from which the
limbs are developed. A vesicle is seen to protrude near the anal end of the
intestine, which, rapidly expanding, spreads over the embryo, acquiring a
close adhesion to the amnion, but remaining distinct from the vitellicle,
over which it spreads. It finally encloses the albumen and interposes itself
between the latter and the lining membrane of the shell. Umbilical vessels
are associated with this membrane. Hunter called this membrane the
allantois from its containing urine, and Owen states that the sac which
surrounds the albumen acts as the chorion or placenta; for it is most
probable that from this surface the albumen is absorbed and the chick
supported on its developmental food. The external part of the sac apparently
acts as lungs as it comes into contact with the shell of the egg through pores
of which there is an exchange of air. Oxygen is consumed and carbon
dioxide is given off. The blood in the vessels of this membrane is in color
more like arterial blood and that in the interior more like venous blood.
The embryonic mass of the incubating egg always floats to the top side.
As the embryo grows it turns upon its left side, exhibiting a profile view; it
then indents the yolk, and finally almost divides it into two parts.
The peripheral layers of cells rise from the margin of the germ mass, and
extend and contract toward the opposite pole. This tract of germ substance
is the primitive streak. Along the median line it next forms a furrow, which
stops short of the ends of the streak. This streak terminates opposite the
point from which the germ begins, and swells into the head. The median
furrow expands upon it. The cephalic borders are next united by a thin layer
of epithelial cells above the furrow, converting it into a cavity, or ventricle.
The myelonal furrow is similarly covered by a layer, uniting the lateral
columns. The embryonal trace becomes longer, narrower, and bends round
the vitellus. A layer of epithelial cells forms a network over the whole
dorsal surface of the embryo. Oblique striæ appear in the broadening germ
mass radiating from the primitive streak. These indicate divisional
segments. These beginnings of aponeurotic septa probably accompany and
support nervous productions from the myelon columns.

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Two transverse constrictions begin to divide the cephalic enlargements
into three lobes, the second and the third of which expand into vesicles. An
accumulation of cells at the side of the middle expansion appears to add
greatly to its breadth. This forms the basis of the eyes.
The differentiation and the confluence of the cell constituents of the
primitive streak have led to the formation of a pair of albuminous cords
along the sides of the median furrow, forming the myelon proper. The cells
exterior to and above them are converted into muscle and fibrous septa; and
beneath the column is a jelly-filled cylinder, with a transversely striated
sheath, pointed at both ends, forming the notocord. Its anterior point passes
a little in advance of the acoustic vesicle. Beneath the notocord and
surrounding the blastema is stretched the vegetative, or mucous, layer of
cells, in contact with the yolk. Both the head and the tail of the now
cylindrical embryo are liberated from the surface of the yolk. A fold of the
blastema, reflected from the under part of the head, sinks like a pouch into
the yolk, and soon includes the rudiment of the heart, like a bent cord,
which begins to oscillate about the seventh day. From the midline of the
inferior surface of the embryo, or its mucous layer, two longitudinal plates
descend, diverging into the yolk-substance, and form the primitive intestinal
groove.
The ophthalmic vesicle elongates and curves outward until the two ends
almost come into contact. Between these two ends and beneath the delicate
tegumentary layer connecting them the crystalline lens is formed. About the
same time, the otoliths appear in the acoustic vesicles, which have now
acquired a cartilaginous case. The cerebral lobes begin to be formed by a
small fold, rising laterally and overlapping the forepart of the second
enlargement, which has expanded to greater breadth. The olfactory cavities
appear as small cutaneous follicles.
The two myelonal columns, expanding between the ear sacs and receding
so as to show the notocord beneath, bend upward and inward, and unite, to
be continued into the posterior of the optic lobes, thus commencing the
cerebellar bridge across the epencephalic ventricle. The encephalic
vacuities have begun to be filled by the granular basis of the cerebellar
substance.
The intestinal groove begins to be converted into a canal at its two ends.
Beneath the anterior end, and behind the heart, there gradually accumulates

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the cellular basis of the liver.
The commencement of the development of the organ of hearing is by a
superficial depression of the cephalic blastema to meet the process from the
encephalon, which forms the acoustic nerve. The lining of the depression
becomes, on closure of the slit, the proper tunic of the labyrinth.
The vesicle of the labyrinth swells into four dilatations, of which three
are ampullar and the fourth cochlear. The ampullar dilatations extend into
very slender canals, at first almost in the same plane, by which they are
brought into mutual communication. As the canals expand and elongate,
they assume their characteristic relative positions as external, superior, and
posterior, the posterior end of the external canal being extended beneath the
posterior canal. The cochlear dilatation curves as it elongates. An inner
layer becomes distinct from the common membrane and forms the acoustic
lamina.
As in the development of the ear, so in the development of the eye, the
production of the nerve process from the cerebral center is the first step; the
infolding of the superficial blastema to meet the nerve is the next. The so-
called cutaneous follicle becomes a circumscribed sac or vesicle, in which
the changes and the development next proceed, converting the vesicle into
an acoustic labyrinth or into an eyeball. In each case neural elements of two
vertebræ become modified to lodge and to protect the sense organs, forming
respectively the recess called otocrane and that called the orbit. The one is
located between the occipital and the parietal vertebræ, and the other
between the frontal and the nasal vertebræ. The part of the outer blastemal
layer of the head which sinks to meet the process from the mesencephalic
dilatation, rapidly changes its follicular into a vesicular state. The vesicle
thus formed elongates, bending around the cell mass in which the
crystalline lens is formed, and the meeting of the two ends results in
forming the choroid fissure at the lower part of the eyeball.
The mesencephalic process, or optic nerve, expands at the posterior of
the circular sac, and, in the course of mutation into eyeball, lines its
posterior part with a layer which becomes the retina. The transparent layer
covering the forepart of that sac and the inclosed lens is formed into the
cornea. Other layers of the sac are formed into the choroid, the ciliary
processes, the iris, and the pecten.

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Of the appendages of the eye the membrana nictitans is the first to
develop. Then develop the lower lid and, last, the upper lid.
After the development of the essential organs of sense, the skin is
developed. Modifications of the skin form the outer ear and the eyelids.
Then are formed the maxillary arch, the hyoidean arch, and the scapular
arch.
The vessels which return the blood from the vitellicle are the transverse
and the longitudinal vitelline veins. The first are so called because these
trunks pass to the embryo at right angles to its axis. They are the largest
returning canals. The longitudinal veins extend parallel with the axis of the
embryo; they are of smaller size. The right anterior longitudinal vein
becomes the right precaval and receives the remains of the right transverse
vitelline vein, as the right vena azygos. The left anterior longitudinal
vitelline vein is also persistent as the left precaval, and enters in the mature
bird, as in the embryo, at the posterior or the lower part of the auricle. The
left transverse vitelline vein is also subsequently reduced, by receiving only
the vertebral veins of that side, to the condition of a so-called azygos vein.
The main trunk of the post-caval is the result of the returning vessels from
the abdominal viscera and the posterior limbs at a later stage of
development. There is but one principal posterior longitudinal vitelline
vein, and this anastomoses with the left transverse vein as it enters the
embryo.
The auricle, which, by its dilatation of the left side, appears to be double,
receives the venous blood at its right division. The left one, subsequently
receives the veins from the lungs, is ultimately separated from the left
precaval and the right auricle to which that vein is conducted and restricted.
The ventricular part of the heart, at the second day of incubation, is in
the form of a bent tube, curving from behind downward, forward, to the
right and upward, continuing insensibly into the part representing the aortic
bulb, in which the septum first appears, and ultimately dividing the
ventricle into two.
At this stage the piers of the maxillary arch appear as buds from beneath
the eyeballs. The naso-premaxillary process is above their interspace. The
piers of the mandibular arch and those of the hyoidean arch follow in close
succession. The blastemal base of the scapular arch projects slightly at the
sides of the fovea cardiaca; the piers, now separate, ultimately meet in front

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of the heart, and accompany it in its retrograde course. The mesencephalon
is the largest of the segments of the brain which are connected with the
eyeballs.
When the heart has assumed its form as such, distinct from the great
trunks rising from it, the two arteries from the base of the ventricles appear.
The artery to the right bifurcates, one division supplying the head and the
wings, the other winding over the right bronchus. That to the left also
bifurcates. Its left division arching over the left bronchus and anastomosing
with the right arch a little below and behind the apex of the heart. Its right
division arches over the back of the heart, bending to the right and
anastomosing with the right aortic arch just above the outer ductus
arteriosus. Each of these divisions of the left primary arterial trunks sends
off a branch to its corresponding lung. As the lung expands, and especially
at the beginning of the act of expansion toward the close of the period of
incubation, the blood is diverted into the pulmonary vessels, and the
channels below them shrink and disappear. The left primary artery is
retained as the trunk of the pulmonaries, and, through the changes in the
interior of the ventricle, this artery comes to discharge exclusively the
ventricle corresponding to the right in mammals. The retained aorta rises
from the left ventricle.
The air-sacs begin at the lower point of the lung, appearing like small
hydatids, and extend further and further into the abdomen, in front of the
kidneys. They are at first full of fluid. Soon after the development of the
abdominal air-sacs others are developed.
The lungs are at first free, but afterward begin to be attached to the ribs
and to the spine.
In the female embryo we first observe two oviducts, one on each side of
the basis, or stroma of the ovarium, which appears in a relation to the
primordial kidneys similar to that of the testes in the male. At the period
when the permanent kidneys have sent their ureters to the cloaca, the
oviducts have been developed as prolongations from that part, and, up to a
certain point of development, they are of equal size and length.
Subsequently the left oviduct alone continues to grow; the right remaining
stationary or shrivels; occasionally it may be discerned as a rudimentary in
the mature bird, but usually all trace of it has disappeared before hatching.
The left oviduct expands above or at its free end into the infundibular

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orifice, where its parietes are very thin. As it descends, these increase in
thickness, and the efferent tube gradually acquires the texture and form of
an intestine. It is attached and supported by a duplicature of the peritoneum.

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Fig. 82.—Embryological studies.

A. 1, The chorion and allantois. 2, The
allantoic cavity. 3, The amnion. 4, The
yolk sac. 5, A small quantity of
remaining albumin.

B. Brain tube of a chick 25½ hours old
showing partly closed brain tube with
eleven folds of neuromeres.

C. The development of the alimentary
tract. 1, Trachea. 2, Lung. 3, Esophagus.
4, Stomach. 5, Pancreas. 6, Bile duct. 7,
V-shaped loop of midgut. 8, Cloaca. 9,
Vitello-intestinal duct.

D. 1 to 6 inclusive, same as C. 7, Cæca.
8, Cloaca.

E. Kidneys, Wolffian bodies, and testes
of an embryo chick. 1, The adrenals. 2,
The genital. 3, Primitive oviduct. 4,
Permanent kidney. 5, Ureters. 6, Duct of
primitive kidney which conducts the
excretion into the cloaca.

F. A transverse section of a chicks’ head

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48 hours of incubation. 1, Forebrain. 2,
Pigmented layer of retina. 3, Ectoderm.
4, Nervous part of retina. 5, Optic stalk.
6, Invagination of ectoderm to form the
lens rudiment.

At first, the right and the left ovaria are similar in size, but the symmetry
is soon disturbed by concentration of development in the left ovary. The
right ovary remains stationary and ultimately, in most birds, completely
disappears by the time the chick is ready to emerge from the shell.
Three fetal membranes are developed, the chorion, the amnion, and the
allantois. There is also developed the yolk sac (Figs. 82 and 83). The
amnion is connected to the body wall at the umbilicus. The amniotic fluid is
found in this sac. The chorion is at first surrounded by the albumen, but as
the albumen is absorbed the chorion comes in contact with the inner shell
membrane. It is probable that the chorion consists of ectoderm on the
outside and of mesoblast on the inside. The amnion, on the other hand, is
formed of mesoblast on the outside and ectoderm on the inner, or
embryonal, side. The allantois springs from the embryo soon after the
fourth day, and develops from the ventral wall of the primitive gut. By some
embryologists, the yolk sac is included in the embryonic membranes. It
commences as the splanchno-pleure surrounding the mass of yolk. It
becomes smaller as the yolk is absorbed. At first its outline is round but
later its walls become folded in. The yolk is dissolved and absorbed by the
entodermic lining of the sac, and is carried to the embryo by veins called
the vitelline veins (Fig. 83, No. B, 4), which ramify on the walls of the sac.
Some time after the fourteenth day, the chick assumes a position
lengthwise within the egg shell so that the head is near the broad end of the
egg. The head is bent upon the chest and the beak is usually tucked under
the wing. Later the head assumes a position, by a double curve of the neck,
so that the beak is in contact with the air cell. About the fifteenth day, the
coils of intestine, which heretofore have been outside the abdominal cavity,
are withdrawn into the abdominal cavity, as is also the abdominal yolk sac.
As the chick pips out of the shell, the umbilicus becomes occluded.
The outer upper part of the tip of the beak is provided with a short, stout,
spike-like arrangement, called the egg tooth. On the twentieth day this part
of the beak is forced against the wall of the egg and gradually breaks

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through the egg shell. The breathing by the lungs commences some time
before hatching; this is evidenced by the chick within the shell giving
chirping sounds.

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Fig. 83.

A. Longitudinal section of chick, 4 days
incubation. 1, Cephalic fold. 2, Caudal
fold. 3, True amniotic cavity. 4,
Epiblast. 5, Somatic mesoblast. 6,
Visceral mesoblast. 7, Hypoblast. 8,
Future anua still closed. 9. The allantoic
vessicle. 10, The mesentery. 11,
Intestine. 12 and 13, Yolk sac. 14,
Cavity of true amnion. 15, The mouth.
16, Pleuroperitoneal cavity. 17, Fore
gut.

B. Membranes of the chick at the third
day of incubation. 1, Membrane
surrounding albumin. 2, Amnion. 3,
Allantois. 4, Vitellicle.

C. The fore part of an embryo chick at
the second day. 1, Mesencephalon. 2,
The eye. 3, Olfactory organ. 4,
Mandibular arch. 5, Maxillary arch. 6,
Maxillary arch. 7, Hyoidean arch. 8,
Scapular arch. 9, Depression organ of
hearing. 11, Process from encephalon
for union with nerve of hearing.

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D. Primitive blood-vessels at second
day of incubation (Owen). 1,
Mesocephalon. 2, The right anterior
longitudinal vein. 3, The eye. 4, The
mandibular arch. 5, The hyoidean arch.
6, Scapular arch. 7, The same. 8, The
ventricular portion of the heart. 9, The
right transverse vitelline vein. 10,
Posterior longitudinal vitelline vein. 11,
Vertebral vein. 12, Tributaries of same.
14, The auricle. 16, Aortic bulb.

E., A transverse section of chick
embryo, 29 hours incubation. 1, Neural
canal. 2, Neural crest. 3, Somatopleure.
4, Splanchnopleure. 5,
Omphalomesenteric vein. 6, Aorta. 7,
Notocord. 8, Pleuroperitoneal cavity.

F. Chick embryo at the ninth day of
incubation. 1, Allantois. 2, Amnion. 3,
Air cell at large end of the egg. 4, Egg
shell. 5, Outer shell membrane. 6, Inner
shell membrane. 7, Yolk sac. 8, Albumin
(Bradley).

The circulation of the blood is somewhat like the circulation in the fetus
of quadrupeds. The primitive tubular heart (Fig. 83, No. D, 8) is bent in S-
shape; the two ends are connected with blood-vessels; and later, by the
development of the septa, the cavities of the adult heart are defined. The
foramen ovale is found in the median septum. This opening brings the right
and the left side into communication. The septa between the cavities of the
heart are completed by the end of the sixth day. The two vitelline, or
omphalo-mesenteric, veins carry the blood containing the nutrients from the
yolk sac to the liver, where it is mixed with the blood drained from the
intestines by the portal vein, and this blood is finally carried by the
posterior vena cava into the right auricle of the heart. From here it passes
through the foramen ovale to the left auricle; from the left auricle it enters
the left ventricle, from which it is forced into the aorta, and then out into the
systemic circulation. Practically all, if not all, of the blood of the pulmonary
artery is sent into the aorta through a connection with this vessel called the
ductus arteriosus.

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Down appears about the thirteenth day of incubation. There are two kinds
of down on the chick, one long, which comes first, about two or three days
before hatching; a second, or fine, down forms at the roots of the other. As
the embryo develops the air cell, at the large end of the egg which is
developed between the two shell membranes, or membranæ putaminæ,
gradually enlarges.

Page 365

OUTLINE FOR LABORATORY STUDY OF
THE CHICK
The objects of laboratory study of the embryos are as follows:
1. To study the living embryo.
2. To study the entire embryo:
With the dissecting microscope, as an opaque object.
With the compound microscope after killing, hardening, clarifying, and mounting.
3. To study embryos by dissection, in later stages.
4. To study the serial sections with the compound microscope.

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THE LIVING EMBRYO

The egg is opened under warm physiological salt solution: 0.8 per cent.
sodium chlorid in distilled water heated to a temperature of 38°C.
Gradually pick away the shell at the large end. Note that there are two
membranes and an air cell. Strip off the membranes. When sufficient shell
and membranes have been removed from the large end, invert the open end
of the egg in the salt solution and allow the contents to flow out. Care must
be taken not to break the yolk. The embryo, or blastoderm, lies upon the
surface of the yolk, which is usually turned with this body uppermost.
Separate the blastoderm by cutting around the outside of the area vasculosa.
In doing this a small pair of slightly curved scissors is needed. After the
embryo, or blastoderm, has been separated, gently float it into a watch
crystal with the flat bottom submerged in the salt solution. The watch
crystal with its contents may now be gently lifted out. Next remove the
vitelline membrane. The vitelline membrane is the delicate transparent
membrane covering the blastoderm, The embryo is now ready for study.

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THE PREPARATION FOR STUDY OF ENTIRE EMBRYOS
AND SECTIONS

The following processes may be used in killing embryos up to four days,
or ninety-six hours, of age. After removing the embryo as described above,
spread the blastoderm out in the watch crystal and pipette off the salt
solution. Allow it to stand till the edge of the tissue begin slightly to adhere.
Then slowly add the killing fluid by aid of a pipette, dropping it on the
center of the embryo. The pipette must be held low or the mechanical
interference will dislocate the parts.
Older embryos are submerged with their membranes intact into the
killing fluid. The quantity of fluid should be several times the bulk of the
specimen. Kleinenberg’s picrosulphuric acid may be used as a killing fluid.
This fluid is a saturated solution of picric acid plus 2 per cent. sulphuric
acid, to which is added twice its volume of water.
Chick embryos from one to two days old should be left in this fluid from
one and one-half to six hours. Embryos from two to four days old two and
one-half to six hours. Remove the specimen from the killing fluid, and
place it in 70 per cent. alcohol. Change the alcohol every twenty-four hours
until the color ceases to come out of the embryo. Preserve in 80 per cent.
alcohol.
If the specimen is to be mounted whole, transfer it from 80 per cent., then
to 50 per cent., then to 35 per cent., and, finally to water. Small embryos
should remain in each fluid thirty minutes and large ones sixty minutes.
The following method may be used for staining embryos: Dilute
Delafield’s hematoxylin with four times its volume of water. To every 6
cubic centimeters of this diluted hematoxylin, add one drop of
Kleinenberg’s undiluted picrosulphuric acid, and leave specimen in the fluid
thus prepared until it is stained through. This will require from one to three
hours. Now pass up through the series of alcohols to 70 per cent. Next
extract the excessive stain with 1 per cent. hydrochloric acid in 70 per cent.
alcohol. Wash repeatedly with 70 per cent. alcohol to free from the acid;
then transfer the specimen to 80 per cent. alcohol and leave in this for
several hours for complete removal of the acid; then transfer to 95 per cent.

Page 368

alcohol for thirty minutes. Allow the specimen to remain in absolute alcohol
for one hour. Introduce a layer of oil of cloves or xylol beneath the alcohol.
This may be done by gradually allowing the fluid to run down the side of
the bottle. After the embryos have sunk into the oil and begun to appear
transparent, remove the fluid and add fresh oil. After the specimen is
sufficiently transparent, mount in balsam, supporting the cover slip so that it
will not rest on the embryo.
In staining for section, place the embryo in borax carmine from the 50
per cent. alcohol and leave twelve hours. Then wash in 50 per cent. alcohol;
after which transfer to 70 per cent. alcohol for six hours. Clarify in oil of
cedar or oil of cloves, and place in melted paraffin for two hours. Imbed in
paraffin, and section.
Embryos may be hardened, imbedded, and sectioned after the usual
methods, using either paraffin or celloidin, and the sections stained with
hematoxylin and eosin after sectioning.

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POINTS TO BE OBSERVED IN THE STUDY

1. The embryo twenty-nine to thirty-four hours old with from ten to
fourteen somites.

A study of the egg.
In opening the egg, observe that the shell membranes are double.
Observe that the shell is porous.
Note the air cell at the large end of the egg and note that the space or cell
lies between the outer and the inner shell membrane.
After the egg contents have dropped into the salt solution, note extending
from the ends of the yolk the twisted denser cords of albumen. These are
the chalazæ, which act as stays to the yolk. Note that the yolk is surrounded
by a delicate membrane. This is the vitelline membrane. The yolk is the true
ovum and serves as food for the developing embryo.
A study of the living embryo.
Note the amount of yolk that is covered by the blastoderm. Note the
slipper-shaped, transparent center of the blastoderm. This is the area
pellucida. In the center of this there is a narrow white streak. The area opaca
is the area lying external to the area pellucida. In this there is the area
vasculosa.
A study of the embryo entire, including the vascular area.
The blood islands show as irregular deeply stained masses in the vascular
area. At this stage they are inclosed in wide anastomosing tubes, the extra-
embryonic blood-vessels, which open peripherally into the bounding sinus
terminalis.
The following structures may be identified:
The neural tube forming the axis of the embryo. In the anterior region
may be noted the forebrain, the optic vesicles, the midbrain. The hindbrain
is subdivided into the neuromeres. The cord, or myelon, of the neural tube
back of the hindbrain is closed in front but is open behind.
The head projects above the blastoderm. The fold which unites the
ventral surface of the head with the blastoderm is called the head fold.

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The diverging folds of the myelon encloses the primitive streak.
On each side of the neural tube are the mesoblastic somites. The series is
continued behind by the undivided segmental plate.
The heart is beneath the hindbrain. The portion of the body cavity in
which it lies, is bounded in front by the head fold and behind by the
diverging limbs of the splanchno-pleure. Its posterior or venous end
receives the vitelline veins from the vascular area. The anterior or arterial
end is prolonged into the ventral aorta.
Note that the axis is somewhat bent.
The head fold of the amnion is noted to extend over the anterior end of
the head.
A study of the transverse sections.
The sections about 20 micro-millimeters thick should be cut serially, and
so mounted. Knowing how many micro-millimeters the embryo is in length
will enable one to make a diagram of the fetal structure in the study of the
series of transverse sections. The sections should be drawn in the order
studied so as to obtain relative structural ideas.
With the microscope study the following regions:
1. Optic vesicle.
2. Midbrain.
3. Posterior half of the heart.
4. Myelon in the closed region.
5. Myelon in the open region.
6. Through the primitive streak.
2. The embryo twenty to twenty-four hours old with from two to six
somites.
Compare the parts in this embryo with those of the embryos from twenty-
nine to thirty-four hours old. Note and describe the relations of the embryo,
the area pellucida, and the area opaca. Note how much of the yolk the
blastoderm covers.
In studying the entire embryos, note the condition of the medullary plate.
Observe if the tube is formed in any part; how far back the head plate
extends, if the heart can be seen; and if the primitive streak is longer or
shorter than in 1.

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Study relations of structures and make drawings through the point of
divergence of the walls of the fore gut; also through the somatic region, and
through the primitive streak.
Study all parts, as the head fold, the heart, and the fore gut.
3. The embryo forty-four to forty-eight hours old with twenty-four to
twenty-nine somites.
Remove the embryo with the entire area, and preserve it.
Note and carefully describe the changes visible to the naked eye since the
thirty-fourth hour.
In making a study of the entire embryo we note there has been a rapid
growth of the dorsal surface of the head, which has become more bent. This
bend, in the region of the midbrain is called the cephalic flexure. The
forebrain and part of the midbrain form almost a right angle with the rest of
the head. The head is compressed laterally and free from the blastoderm.
The dorsal side of the trunk is turned up, and there is a twisting of the axis
of the embryo just back of the heart. The tail fold begins at about this time
and may or may not be visible. The optic vesicles are relatively smaller in
relation to the brain than in 1. Note the part of the forebrain to which they
are attached. Observe the inner and outer layers of the retina, the lens, the
choroid fissure, and the cavity of the vitreous humor.
Note the auditory vesicles and whether or not they are closed sacs.
Note that the heart has grown in length and has become doubled on itself.
The two ends are fixed. Note the relation of the heart to the afferent and
efferent blood-vessels. Note that two, and possibly three, visceral pounches
are visible. Note whether or not they are ventral to the midbrain. The first,
the hyomandibular pouch, is bounded in front by the first visceral, or
mandibular, and behind by the second visceral, arch. The second pouch is
bound in front by the hyoid, and behind by the third visceral arch. The third
pouch is bounded in front by the third visceral arch, and behind by the
fourth. Note the number of mesoblastic somites and the condition of the
mesoblastic segmental plates.
Note how far back the foregut is closed. Locate the head fold of the
amnion, and note how far back it is closed. Note changes that have taken
place in the vascular area. In studying the sections it will be found that a

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section cut transversely to the trunk will pass horizontally through the
forebrain and through the midbrain.
Study a section through the trunk a short distance behind the heart.
Observe the elevation of the axis of the body. Note the way in which the
lateral folds, or the lateral limiting sulci, in the somatopleure, delimit the
embryonic from the extra-embryonic area.
Note the appearance of the mesenchyme, the approximation of the two
dorsal aortæ, the appearance of the amniotic folds. Observe in the
mesoderm the posterior cardiac veins, and the myotomes, or muscle plates.
The sclerotome is made up of the mass of mesenchyme between the
myotome, on the one hand, and the neural tube and the notochord, on the
other. Note the folding of the splanchno-pleure, and note if there is present
the Wolffian duct, or the nephrotome.
Study sections through the optic vesicles. Note if there is the beginning
of the lens. Do you note the diverticula of the pharynx? Can you identify
the closed amnion and the chorion?
Study sections through the auditory pit. Note fusion of the gill pouches
with the ectoderm. Note the blood-vessels. Study sections through the
region of the heart, through the roots of the vitelline veins, and through the
primitive streak, if it is still present.
For this study it will appear that the anterior end has developed in
advance of the posterior end. The tail fold has probably just begun.
Write a description of the pharynx, and of the circulation at this stage.
4. The embryo sixty-eight to seventy-two hours old with cervical
flexures formed.
In a study of the living embryo note the changes visible to the naked eye
since forty-eight hours old. Note the difference in the blood-vessels of the
vascular area. Name the arteries and veins. Note the beating of the heart.
In a study of the entire mount note that a second, the cervical flexure, has
appeared in the head. Note that the tail fold is well formed. Note the
position of the embryo on the blastoderm. Determine if the amnion is
completely closed. Note the olfactory pits on the ventral surface of the
head, a short distance in front of the optic stalks. Note the telencephalon, a
rudiment of the cerebral hemispheres and an extension of the primary
forebrain. It is bilobed anteriorly. The optic stalks are attached to the floor

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near the anterior end of the thalamencephalon. Note the infundibular region,
which is the depressed region behind the optic stalks. In the roof of the
thalamencephalon there is a short diverticulum, the epiphysis. The
mesencephalon, or midbrain, forms the apex of the cranial flexure, and is
united to the hindbrain by a narrow isthmus. The metencephalon, or
rudimentary cerebellum, appears as a thick portion on the most anterior
division of the hindbrain. The rest of the hindbrain is provided with a
transparent roof and constitutes the myelencephalon, or the rudimentary
medulla oblongata. Observe the inner and the outer wall of the optic cup,
the lens, the choroid fissure, and the posterior, or vitreous, chamber.
Note the form of the otocyst, or auditory sac. Note above which visceral
arch it lies. Note the number of visceral clefts. The visceral arches are
formed by the thickening of the walls of the bounding clefts. The visceral
arches are as follows: the first is the mandibular, or hyomandibular, arch,
which is in front of the first cleft. From this there is developed the lower
jaw. Note if there is a maxillary process arising from the dorsal angle of the
arch. The second arch is the hyoid arch, which is located behind the first
cleft. Then follow in order the third, the fourth, and the fifth visceral arches.
Note above the mandibular arch the rudimentary trigeminal ganglion, and
above the hyoid arch the rudimentary acoustico-facialis. The latter is in
contact with the anterior walls of the auditory sac. The rudimentary glosso-
pharyngeal ganglion is noted above the third visceral arch. The vagus, or
pneumogastric, ganglion is located above the fourth and the fifth. Note the
form and the position of the heart. Note the anterior and the posterior limb
rudiment in the trunk.
In a study of the sections it is found that cuts transverse to the trunk pass
about horizontally through the forebrain. At this age the following sections
of the embryo should be studied:
First, through the hindbrain, at which level will be noted the auditory
sacs, the neuromeres, the trigeminal, the acoustico-facialis, and the glosso-
pharyngeal and the vagus ganglion.
Second, through the upper part of the pharynx, at which level will be
observed the midbrain, the hindbrain, the visceral pouches, the nerves, and
the blood-vessels.
Third, through the choroid fissure of the optic cups. Note the parts of the
eye, and, on the other side of the section, the heart.

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Fourth, a study of a section through the olfactory pits.
Fifth, a study of a section through the pancreatic and the hepatic
diverticula.
Sixth, a study at the beginning of the allantois through the hind-gut.
At this age it is of interest to study the systems of organs. Observe the
manner in which the splanchno-pleure folds to form the walls of the
intestine. Note the commencement of the mesentery. Note that the foremost
part of the alimentary tract is formed from the stomodeal invagination of
the ectoderm. The hypophysis is formed from a dorsal outgrowth of this.
Note its relation to the brain.
The following structures are formed from outgrowths of the ectoderm at
this stage:
First, the visceral pouches.
Second, the median rudiment of the thyroid. This is an outgrowth from
the pharynx between the two hyoid arches.
Third, the rudimentary lungs, which develop in a pair from a median
ventral diverticulum of the alimentary tract, just behind the last visceral
pouch. The esophagus is just posterior to this. The esophagus, very short at
this stage, is continuous with a slightly wider part that develops into the
stomach.
Fourth, the first liver diverticulum, and, at a short distance posterior to
this, the second liver diverticulum.
Fifth, the pancreas is at a point where the intestine opens ventrally. It first
appears as a slight thickening of the dorsal angle of the intestine.
Sixth, the ventral wall of the hind-gut forms a wide evagination.
Seventh, the beginning of the allantois.
After the whole series of transverse sections have been studied and
drawn, construct a longitudinal section of the fetus, including a
reconstruction of the alimentary tract.
At this stage the heart is a simple tube. The following divisions are
distinctly visible: the auricular portion, the ventricular portion, the sinus
venosus, and the bulbus arteriosus. The union of the two ductus Cuvieri and
the ductus venosus form the sinus venosus. The two ductus Cuvieri are
formed by the union of the anterior and the posterior cardinal veins. The

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ductus venosus is formed by the union of the small right and the large left
vitelline vein. These latter veins return the blood from the yolk sac. The
sinus venosus empties into the single auricle above which it is located. The
single auricle is later divided into two chambers, the right and the left
auricle. At this stage it is widest in the lateral direction. The auricle empties
directly into the ventricle. The ventricle lies ventrally and behind the
auricle. This location is due to the bending of the heart at this stage of
development. Its hindmost portion forms the future apex of the heart. If the
series of sections be studied from the posterior forward, the ventricle will be
first to appear in the sections. Just beneath the auricular portion of the heart
there is the bulbus arteriosus. The bulbus arteriosus soon divides into a
number of aortic arches. There is an ascending pair in each of the visceral
arches. The dorsal aorta is formed by the union of the aortic arches above
the visceral arches. The aortic arches are first continued a short distance
forward as the carotid arteries. The dorsal, or posterior, aorta passes
backward under the notochord. The dorsal aorta divides into two parallel
aortæ which give off on each side the vitelline arteries. Note other branches
of this aorta.
The veins at this stage consist of the anterior and posterior cardinal, the
ductus venosus, the ductus Cuvieri, and the vitelline veins.
Make drawing of the circulatory system after a completion of the study
of the series of sections.
Make a study of the nervous system according to hints already given.
The dorsal and the ventral roots of the spinal nerves are given off
separately, and secondarily unite. From the neuroblasts of the cord there are
at regular intervals outgrowths representing the ventral roots. From the
neural crest there develop segmental collections of neuroblasts which form
the spinal ganglia, from which the dorsal spinal nerve roots develop. In fact
this developmental stage can be observed in embryos only forty-eight hours
old, first appearing as a line of cells springing on each side from the angle
between the neural canal tube and the external epiblast. In the section from
the embryo seventy-two hours old there are observed the rudiments of the
development of these spinal nerves. Four primary ganglia develop in the
neural crest of the head. These ganglia are as follows: the acoustico-facialis
ganglia, which is located over the hyoid arch; the ganglia of the trigeminus,
which is located over the mandibular arch; the ganglia of the glosso-

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pharyngeus, which is located over the third visceral arch; and the ganglia of
the vagus, which is located over the third and the fourth visceral cleft.
In this stage of development the trigeminal and the acoustico-facialis are
clearly visible.
On each side and dorsal to the aorta is noted the Wolffian body, or
mesonephros. The Wolffian body (Fig. 82, E) consists of a series of tubules
imbedded in the mesenchyme. The openings into the Wolffian duct lie just
beneath the cardinal vein.
In a study of the Wolffian duct determine just how far anteriorly and
how far posteriorly it extends. Note whether it empties into the cloaca.
Each tube beginning in a blind extremity is later dilated. It has a thin
wall, and is situated near the median portion of the Wolffian body. The
tubule proper passing transversely, opens into the duct. The upper wall of
the thin walled part is invaginated by a mass of mesenchyme that receives a
small vessel from the dorsal aorta. The Malpighian corpuscle, consisting of
a glomerule and Bowman’s capsule, is thus established. In the study of the
four days old chick note the further development of these parts.
In a study of a chick four days, or ninety-six hours old, note to what
extent the yolk is covered by the blastoderm. It will be noted that the
embryo lies in the extra-embryonic cavity. This cavity is bounded above by
the chorion and below by the splanchno-pleure. In removing the amnion
from the embryo, note the relation to the somatic umbilicus. Note the
relation of the splanchnic umbilicus to the splanchno-pleure. What relation
has the allantois to the above?
In examining the head, locate the cerebral hemispheres, and note their
development. Locate the pineal gland. Note changes in the olfactory pit and
the eye. Locate the lens and the choroid fissure. Note that the maxillary
process of the mandibular arch lies beneath the eye and behind the olfactory
pits. Note the otocyst and the relations of the other arches to the above
structures.
In a study of the trunk, note the tail, the allantois, Wolffian ridges, the
heart, and the condition and the position of the rudimentary limbs.
Make drawing of embryo from the side view. Carefully cut off the head
immediately behind the last visceral arch, and study and draw the structures
observed on the ventral side. Note the maxillary processes, the mandibular

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and the hyoid arch, the nasal pits, and the fronto-nasal process, which is just
beginning its development.
In a study of transverse sections observe from your drawing at what level
the section is made. Study and draw a section made through the region of
the anterior limbs. Note the spinal ganglion, the muscle plate, or myotome,
the condensation of mesenchyme around the notochord, the pancreas, the
liver, and the intestine; and note the distribution of the mesenchyme. Note
the ventral roots of the spinal nerves, and the neuroblasts in the spinal cord.
In sectioning the embryo from before backward, the first sections will
pass horizontally through the hindbrain and the midbrain region. Note the
parts, including the auditory vesicle. In the first series of sections also
locate the ganglia of the pneumogastric, or vagus, the acoustico-facialis, the
trigeminus, and the glosso-pharyngeal nerves. Note the notochord and the
cardinal veins. After the disappearance of the ear, we observe the midbrain,
which, is located at one end of the section, and the cord at the other end.
The region between lies just above the pharynx. In the following series
study the visceral arches. Note the third pair of cranial, or motor ocular,
nerves. This latter nerve springs from the floor of the midbrain. From the
ventral prolongation of the floor of the thalamencephalon there arises the
infundibulum. The hypophysis is located just beneath the infundibulum. At
this stage the hypophysis appears as a tube to empty into the mouth. This is
an ingrowth of the oral epithelium.
In a study of a section through the center of the eye we should observe
the lens and optic stalk. This is in the region of the optic chiasm. Note the
choroid fissure and the pineal gland, the latter appearing just beyond the
eyes. Just forward lies the telencephalon, or rudiments of the cerebral
hemispheres.
In a study of the alimentary tract we note that the mouth is bounded by
the mandibular arches. Note the maxillary processes, and the ventral surface
of the head. A finger-like diverticulum, extending from the roof of the
ruptured double membrane, formerly separating the pharynx from the
arches, forms the hypophysis. The great development of the visceral
pouches makes the pharynx rather complex. In studying sections
horizontally through the pharyngeal region note the various visceral arches
and pouches. Note the arteries of the thyroid diverticulum.

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In the series note the changed development of the lung rudiments, the
glottis, the esophagus, the trachea, and the bronchi. The bronchi appear in
pairs. Note that the liver has assumed proportions, and that it surrounds the
common trunk of the vitelline veins, which it divides into two parts. The
sinus venosus lies close to the heart. The ductus venosus is also surrounded
by the liver. Above the tip of the ventricle we note a dilatation which
represents the stomach. The hepatic, or bile duct is located immediately
behind the stomach. This duct is formed by the fusion of the right and the
left duct. Locate, draw, and describe the pancreas; trace the intestine; locate
the splanchnic umbilicus, or yolk stalk; locate the allantois stalk, and trace
its connection with the hind-gut.
In the series, locate and study the Wolffian ducts, the beginning of the
Müllerian duct, the embryonic kidney, or mesonephros, the permanent
kidney, or metanephros. The urino-genital ridge is made up of all the above
except the last named. The urino-genital ridge forms a rounded projection
on each side of the mesentery into the dorsal angles of the body cavity.
The Wolffian ducts empty into the cloaca. There are two ducts which
may be traced far forward, and which are found to extend backward along
the lateral margin of the ridge to the cloaca. Along the greater part of their
length we note tubules emptying into them.
Beginning near the anterior end of the urino-genital ridge, we note that
the Müllerian ducts arise from a thickened line of epithelium. The greater
part of the ridge is formed by the mesonephros. This is made up of a series
of tubules in each of which we may distinguish two parts as follows: a tuft
of capillaries from the aorta forming the glomerules, surrounded by a thin
walled invaginated capsule, making up the Malpighian corpuscle; and the
tubules proper. The tubules lead from the corpuscles, or glomerules, to the
Wolffian duct.
The germinal epithelium constitutes the essential portions of the gonad,
or ovary, or testis. The germinal epithelium arises from a thickening of the
peritoneum of the median wall of the ridge. The gonad is found near the
anterior end of the ridge. At about this age of the embryo there should
appear the primitive ovary or testis. Near the posterior termination of the
Wolffian duct and from the dorsal diverticulum there arises the ureter, or
metanephros duct.

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In these series there should be studied the heart and circulation, which
will be found similar to the sections from the embryo seventy-two hours
old.
Work out a summary of the relations of the allantois and the yolk stalk to
the intestines; the relations of the Wolffian ducts to the intestines; the origin
of the ureters from the Wolffian ducts; the relations of the lungs, the liver,
and the thyroid gland; the relations of the blood-vessels; a study of the
muscle plates; the relations of epiphysis, hypophysis, infundibulum, mouth,
and pharynx; the relations of the vagus, or pneumogastric, trifacial,
acoustico-facialis, and glosso-pharyngeal nerves to the visceral arches.
In addition to the study of embryos at the end of each of the first four
days of incubation, a study should be made of preserved museum
specimens each of which represents the development of a day up to and
including the twenty-first day.

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THE DERIVATIVES OF THE GERM-LAYERS

From the three primary germ-layers are developed the various tissues and
organs of the body by metamorphoses which may be referred to the two
fundamental processes of specialization, or the adaptation of structure to
function, and of unequal growth, which latter results in the formation of
folds, ridges, and constrictions.
From the ectoderm are produced:
The epidermis and its appendages, including the nails, the epithelium in
connection to the feathers and the feathers.
The infoldings of the epidermis, including the epithelium of the mouth,
epithelium of the salivary glands and the anterior lobe of the pituitary body,
or hypophysis.
The epithelium of the nasal tract with its glands and communicating
cavities.
The epithelium lining the external auditory canal, including the outer
stratum of the membrana tympani.
The lining of the anus.
The epithelium of the conjunctiva and of the anterior part of the cornea,
the crystalline lens.
The spinal cord, the brain with its outgrowths, including the optic nerve,
the retina, and the posterior lobe of the pituitary body.
The epithelium of the inner ear.
From the entoderm are produced:
The epithelium of the respiratory tract.
The epithelium of the digestive tract, from the back part of the pharynx to
the anus, including its associated glands, the liver, and the pancreas.
The epithelial parts of the middle ear and of the eustachian tube.
The epithelium of the thymus and the thyroid bodies.
From the mesoderm are developed:

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Connective tissue in all its modified forms, such as bone, cartilage,
lymph, blood, fibrous and areolar tissue.
Muscle tissue.
All endothelial cells, as of joint-cavities, bursal sacs, lymph sacs, blood-
vessels, pericardium, and endocardium, pleura, and peritoneum.
The spleen.
The kidneys and ureters.
The testicles and the system of excretory ducts.
The ovary and oviduct.

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PREPARATION OF STRUCTURES FOR STUDY

It is hoped that the following suggestions will be helpful in the laboratory
work.
Directions for Dissecting Muscles.—The muscles that are brought into
great play in movements of the bird’s limbs are dark carmine in color, while
those which are not brought greatly into use are pale or white in color.
The tendons are made up of white fibrous connective tissue, are very
dense, and pearly white in color.
In securing a bird for dissection of muscles it is best to select one in
rather poor flesh, as the fat is annoying. The bird may be chloroformed or
killed in a bell jar by aid of illuminating gas. After the bird is dead pluck all
the feathers and immerse it in a 10 per cent. solution of formaldehyde or of
80 per cent. alcohol. It is best to puncture the abdominal wall so that the
fluid may at once fill the abdominal cavity and more readily gain access to
the chest cavity; and to puncture the skin at various points so that the liquid
may more quickly become disseminated among the muscular structures.
Post-mortem changes quickly take place if these precautions are not taken.
The liquid surrounding the carcass should be at least twice the quantity of
the bulk of the carcass.
The first dissection should be to lay bare the dermal muscles. The dermal
muscles are of two kinds, true dermal and dermo-osseous. The dermal
muscles have their origin and insertion in the skin, and control the
movements of the different groups of feathers. The dermo-osseous have
their origin on some part of the skeleton, and insert to the integuments.
The dermal muscles vary with the characteristics of the bird, we do not
find all the known dermal muscles in any one specimen. A cock of the
Cornish breed will show these muscles best developed. Birds possess an
enormous system of minute muscles divided up into an infinite number of
fasciculi, to act harmoniously upon the feather quills and to agitate
collectively the plumage. By the aid of a low-power lens the action of the
feather muscles in the large quill butts of the wing or the tail may be
studied.

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The muscles may be studied in groups as outlined in the text. Make an
incision through the skin down to the bone on the superior part of the head,
parallel and close to the base of the upper mandible, and extending
completely across. From the outer end of this make an incision backward
and down to the skull and posteriorly. The muscles of the upper part of the
neck will then be exposed. The straight incision should extend to about a
half inch on the inside of the upper eyelid of the same side. Reflect the flap
of skin from the top of the skull, and carefully examine the under side of it
in the median line, where it overlies the frontal region. The dermo-frontalis
will be observed if it be present. In many birds, especially in females, it
may not be discernible, and may be considered absent. To expose the
circumconcha make an incision completely around the ear; then carefully
dissect to the ear base. A dermal circular muscle should be observed. To
expose the dermo-temporalis extend the longitudinal incision down the
back of the neck to a point between the clavicular heads, carrying it just
through the skin and about one-fourth of an inch to the side of the median
line. Remove the skin from the throat and the anterior portion of the chest.
Lay open the alar and parapatagial duplicatures of the skin. This exposes a
number of dermal muscles. The dermo-temporalis is now observed to
extend from a small depression just above and anterior to the temporal
fossa. It makes slight attachments to the temporal muscle, which it covers,
and extends backward as a thin ribbon-shaped muscle, the fibers blending
with those of the cleido-trachealis, and becomes lost upon the skin in front
and opposite the shoulder-joint. At times its fibers blend with those of the
dermo-tensor patagii.
As the musculature of the fowl is loosely arranged, the rest of the
dissection is easily done if care be exercised.
The ligaments may be dissected after the completion of the study of
muscles, using the same subject or, a two pound broiler be prepared by
killing in the gas chamber, plucking the feathers and parboiling just till the
flesh becomes tender and is easily removed, it will be observed that all
structures can be removed from the points exposing the ligaments distinctly.
The ligaments appear swollen and more easily observed for study.
Directions for the Study of the Viscera.—Carefully remove the right
and the left abdominal and thoracic walls, allowing a strip of tissue to
remain in the median line to hold the organs in their normal position. To

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open these cavities it is necessary to use the bone saw and the scalpel. The
organs may now be studied from each side. To make a longitudinal section
through the median line, select a small bird, one weighing not more than 2
pounds, kill, and preserve in a 10 per cent. solution of formaldehyde for
three days. Then with a sharp, thin, long-bladed knife make an incision at
one sweep through the median line of the body down to the back bone, and
with the bone saw section through the vertebræ. If it is difficult to cut
through the breast-bone, saw through before making the incision. In small
birds the entire cut may be made without the aid of the saw.
Directions for the Study of Arteries.—Arteries should be injected.
Veins are usually more or less filled with blood so that the tracing of these
is not so difficult as the tracing of uninjected arteries. Nerves are white and
no difficulty is usually encountered in tracing them.
The courses of arteries, veins, and nerves are side by side, and many of
them, as in mammals, are arranged in the order of veins, arteries, nerves,
the veins being in front.
The injection apparatus consists of the following parts: air-compression
chamber, to which is attached a pressure pump. A manometer made of glass
tubing 6 millimeters in diameter, inside measurement. This tube is partly
filled with mercury, and a scale in centimeters is made from the top of the
right-hand tube (Fig. 84, No. 8). This ruling, or gauge, should be about 15
centimeters long. Extending from the right extremity of the U-tube is a
small rubber tubing which is attached to the chamber containing the
injection fluid; and extending from the inferior part of this chamber is
another tubing which has the injection needle attached to the free end.
The injection should be done under 120 millimeters pressure. The stop
cock of the pressure chamber is released sufficiently to raise the mercury in
the U-tube six centimeters, which multiplied by 2, the amount of work
required to raise two columns, makes 120 millimeters pressure. If this
pressure be maintained, all vessels should be injected without rupture. The
same process may be used in injecting the air cells through the trachea.
The injecting material may consist of one part finely sifted plaster of
Paris, four parts water, and sufficient gentian violet to make a violet color.
For the coloring, red aniline may be used in preparing this material. The dye
should be dissolved in the water to be used in making the injection liquid.
Caution must be used and the work rapidly done, as the plaster soon sets, or

Page 385

becomes solid, in the needle or in the tubing. A small cannula should be
used, since the endothelial lining of the arteries are easily injured and
difficulty may thus be created.
Select for arterial dissection an old cock, as in a bird of this kind the
arteries are larger and the difficulties are reduced. Select for bleeding and
injection the ischiadic artery in the thigh region. With the sharp point of the
thin blade of a knife make an incision lengthwise of the artery being careful
not to strip back the endothelial lining of the artery. Allow as much of the
blood as will escape before injecting; in fact, the arteries should be
thoroughly emptied, so that there is no longer danger of a clot’s plugging
some vessel and thus preventing its filling. Since the blood of most birds
coagulates in about thirty seconds, this work must be done rapidly, care
being exercised to keep the flow running as long as possible. After bleeding
is completed, insert the cannula and tie the vessel tightly around the cannula
to prevent the escape of the injecting fluid. See that all connections are
sufficiently tight to prevent the escape of liquid under pressure. After the
injection is completed, remove the cannula and tie the artery with a small
twine, preferably cotton. Quickly remove all injecting fluid from the needle,
the tubing, and the injecting chamber.
During the operation of bleeding the cock may be chloroformed, care
being taken not to administer chloroform to kill him; for it is necessary to
maintain life as long as possible so that the heart may be kept beating and
all blood possible drained from the arteries. After the injection is completed
the bird may be plucked and immersed in the preservative fluid in the same
manner as in the preparation for dissection for muscles.
The arteries, the veins, and the nerves may now be dissected and studied
in relation to one another and in relation to the muscles, the bones, and
other structures. The skin should not be removed from the shanks till it is
desired to dissect these parts, as the tissues quickly dry out. In fact, the
tendons of the shanks and toes can best be dissected while the specimen is
fresh.
A Study of the Structure of Bones.—Longitudinal and transverse
sections of old bone may be made by making thin longitudinal and
transverse sections with the bone saw, and then by making them very thin
with a fine three-cornered file. Examining under the low power microscope,
we note the lacunæ, the canaliculi, and the Haversian system.

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Similar sections in green bone may be studied if prepared as follows.
Secure specimen of bone just removed from a fowl and place it for three
days in a 10 per cent. aqueous solution of hydrochloric acid. Test by
puncturing with a needle, and, if all the mineral salts are removed, place in
a water bath and wash for four hours. Pass it through the fluids usually
employed in preparing specimens for sectioning with the microtome. Stain
as sections of other tissue for microscopic study. See the description below.
If the ends of the bone be included, it will enable the student to study not
only compact bone but also cancellated bone and articular, or hyaline
cartilage, and in some of the bones, as the femur, the red marrow.
Special Technic for the Dissection of Cranial and Spinal Nerves.—It
is rather difficult to dissect the cranial and spinal nerves of the fowl, owing
to the fact that the structures are very small. The bone is rather hard and the
nerve tissue so delicate that great skill must be attained to achieve any
degree of success.
A simple technic has been developed as follows: Place the head and neck,
or other structures of the spinal column in a 10 per cent. aqueous solution of
hydrochloric acid for three or more days, the time depending on the size of
the specimen and the amount of soft structures surrounding it. This solution
removes all the calcium salts from the bone and makes the removal of the
bony structures a less difficult task.
Directions for the Study of Soft Structures.—Secure a specimen of the
tissue to be studied—lung, muscle, intestine, liver, pancreas—from a
normal fowl just killed. The specimen should be not more than ½ inch
square. After first hardening three days in 10 per cent. formaldehyde. Pass
through the following fluids:

1. Alcohol, 95 per cent. 24 hours
2. Alcohol, absolute 24 hours
3. Alcohol and ether, equal parts 24 hours
4. 1 per cent. celloidin 24 hours
5. 2 per cent. celloidin 24 hours
6. 4 per cent. celloidin 24 hours
7. 6 per cent. celloidin 24 hours
8. 10 per cent. celloidin 24 hours
9. Place on block, and as soon as solid, place in 80 per cent. alcohol until ready to section.
Histoloid or parlodion will take the place of celloidin.

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In placing specimen on the block be careful that the specimen lies
conveniently for cutting the sections in the right direction. As soon as the
surface has hardened a little, add a few drops of thick celloidin, and repeat
until there is a good body of celloidin. Allow to stand until the tissues are
quite firmly fastened to the block, but not long enough to permit shrinking.
Then place in 80 per cent. alcohol until the specimen is perfectly firm, 12 or
more hours, before cutting.
All tissues, cut sections, and mounted blocks are to be placed in 80 per
cent. alcohol. As containers for this purpose shell vials will be most handy.
Cut the sections with the microtome as thin as possible, the thinner the
better. The following process of staining will make the nucleus blue and the
cytoplasm reddish.

1. Float section in a tumbler of tap water.
2. Place section on slide, and immerse in hematoxylon for five to ten
minutes.
3. Immerse in acid alcohol from two to five seconds.
5. Place on slide, and immerse in eosin from one-half to three minutes.
6. Wash thoroughly in alcohol.
7. Clarify in oil of cloves, oil of cedar, or beechwood creosote, ten
minutes.
8. Mount in balsam.
9. Label and study.
Delafield’s hematoxylon is prepared as follows:

Hematoxylon crystals 4 grams
Alcohol, 95 per cent 25 c.c.
Saturated aqueous solution of ammonia alum 400 c.c.

Add the hematoxylon dissolved in the alcohol to the alum solution, and
expose in an unstoppered bottle to the light and air for three or four days.
Filter and add:

Page 388

Glycerin 100 c.c.
Alcohol, 95 per cent. 100 c.c.

Allow the solution to stand in the light until the color is sufficiently dark;
then filter, and keep in a tightly stoppered bottle. The solution keeps well
and is extremely powerful. So long as it is good the solution has a purplish
tinge. If time permits, it would be wise to combine the alum, the
hematoxylin, and the water, and to ripen the solution for two or three weeks
before adding the other ingredients, which have a tendency to prevent
oxidation.
The acid alcohol is made as follows:

Absolute alcohol 70 c.c.
Distilled water 30 c.c.
Mix.

Above solution 99 c.c.
Hydrochloric acid 1 c.c.

Eosin is sold in two forms, that soluble in water and that soluble in
alcohol. The eosin soluble in water is preferred, because with it a greater
degree of diffusion in stain can be obtained.
Keep on hand a saturated aqueous solution and dilute with water as
needed. The strength of the solution to be used varies somewhat with the
tissue and the reagent in which it is to be fixed; but usually the strength
should be between ⅒ and ½ per cent. when eosin is used after hematoxylin.
The diluted solutions should contain 25 per cent. of alcohol, otherwise they
will not keep well. When eosin is used before an aniline dye, such as
methylene blue, a 5 per cent. or even a saturated solution should be used.
To Stain Sections of Liver for the Study of Kupffer Cells.—To bring
out this reaction Keys suggests the following technic:
Fix small blocks of the fresh tissue of spleen or liver for eighteen to
twenty-four hours in Müller’s fluid plus 5 per cent. mercuric sublimate.
Imbed in paraffin and section to 4 microns. Fix sections to slide, and stain
twenty to forty minutes with acid carmine. Wash, and transfer to equal parts
of a 2 per cent. aqueous solution of potassium ferrocyanid and of a 2 per

Page 389

cent. aqueous solution of hydrochloric acid. Remove after three to ten
minutes, wash in distilled water, and pass quickly through a 0.5 per cent.
aqueous erythrosin solution. Dehydrate in alcohol, clarify in xylol, and
mount in Canada balsam.
To Prepare Anatomical Specimens for a Museum.—The Keiserling
method gives the best results, since by this method the tissues retain their
normal color. The three steps are as follows:
1. Place the specimen in the following solution and leave from one to
seven days, the length of time depending upon the size of the specimen.

Formalin 200 c.c.
Potassium acetate 30 grams
Potassium nitrate 15 grams
Water 1000 c.c.

2. Pass the specimen through each of the following solutions, leaving it
in each twenty-four hours or until the normal color is obtained. The
specimen should be removed from alcohol as soon as color is attained. If it
is left in the alcohol too long it will again lose some of its color.

Alcohol 40 per cent.
Alcohol 60 per cent.
Alcohol 80 per cent.
Alcohol full strength

3. Place the specimen in the following permanent solution, label, and
place in museum.

Glycerin 40 c.c.
Potassium acetate 40 grams
Distilled water 400 c.c.

A small piece of thymol must be placed on the top of the liquid in each
jar, or mold will develop and spoil the specimen.
To Make Specimens Transparent.—Specimens may be rendered
transparent by the method of Spalteholz.
The steps are essentially as follows:

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I. Preparation of the fresh tissue. If any parts are to be made conspicuous,
as blood-vessels, or the lymphatic system, they must be injected with an
insoluble, unbleachable substance. Spalteholz recommended carmine or
methylene blue, and carbon. I have found Higgin’s ordinary black carbon
ink excellent for this purpose. The system or systems are injected with this
substance while the tissue is perfectly fresh.
II. Fixation. The tissues are fixed preferably in 10 per cent. formalin. The
length of time for fixation depends on the size of the tissue. In formalin it
requires from eight hours upward to fix completely.
III. Rinsing. Running tap water for five or ten minutes accomplishes the
rinsing. If it is impracticable to pass directly into the bleaching fluid, the
tissues may be kept temporarily in 60 per cent. or 70 per cent. alcohol. They
should then be rinsed again thoroughly in water when ready to bleach.
IV. Bleaching. The bleaching fluid used is hydrogen peroxid to which
ammonia is added until a white precipitate forms. The proportion is
approximately two parts of peroxid and one of ammonia. The material is
bleached until all the color is removed and the tissue looks perfectly clear or
slightly opaque. It may be quite transparent as the protein coagulate is
somewhat white, but all yellow or reddish color should be bleached away.
V. Washing. Rinse thoroughly in running tap water or through several
changes of water until the odor of ammonia is quite gone.
VI. Dehydration. Pass gradually through alcohol solutions, 30 per cent.,
50 per cent., 60 per cent., 70 per cent., 80 per cent., 95 per cent., and last
through absolute alcohol. The time required for dehydration will vary with
the size of the material, but in either 95 per cent. solution or in absolute
alcohol the tissue should remain until well hardened, twenty-four hours or
more. Dehydration is completed by passing from absolute alcohol, to a fluid
one-half absolute alcohol and one-half benzol; thence for a few days to pure
benzol.
VII. Clarifying. From benzol the material is finally clarified in winter-
green oil or any other standard clearer, and put up in its final position in the
museum jar.
In commenting on this method Dr. A. F. Contant says: “I have found this
to work very successfully in the injection of the lymphatics of the human
skin, which, as you know, is a rather delicate injection and has been difficult
of demonstration by other methods. With this method, however, I have

Page 391

prepared whole portions, as the side of the face, the leg, etc., of small
animals and embryos which show clearly the whole course of the lymphatic
vessels and nodes, in situ, and their relations to surrounding parts.”

Page 392

EQUIPMENT FOR THE DISSECTION LABORATORY

Figure 84 illustrates some essential equipment for the dissection
laboratory. The equipment should consist of a pump, No. 1, which forces air
through the rubber tube, No. 2, into the pressure tank, No. 4, which is
guarded by the valve at No. 3. A dial, No. 5, indicates the pressure of the air
within the tank. The air as needed is released through an outlet valve. The
air now passes through the rubber tube, No. 6, into the left arm of the
manometer at No. 7. The manometer is simply a glass tubing filled with
mercury to the point indicated at No. 7. By the side of the opposite arm
there is made a scale graduated in centimeters. The tube at No. 9 being
attached to the Y-tube, conveys air under the same pressure into the
injection chamber as that supporting the column of mercury of the
manometer. It is necessary to have a pinch cock, as indicated at No. 11, to
control the liquid within the tube. No. 12 illustrates the tube in the end of
which, No. 13, there is inserted a trocar which is introduced into the artery
and tightly tied with a cord.

Page 393

Fig. 84.—Photograph showing injection
apparatus, dissection instruments,
dissection pan and death chamber.

1, Pump. 2, Rubber tube leading from
pump to compression chamber. 3, Stop
cock. 4, Compression air tank. 5,
Pressure indicator. 6, Rubber tube
leading from pressure tank to
manometer. 7, Top of mercury in
manometer tube. 8, Open end of glass
tube showing scale in centimeters. 9,
Tube leading from 4 to injection
chamber. 10, Injection chamber
containing injection fluid. 11, Pinch
cock on rubber tube connecting
injection chamber with injection canula.
12, The tube. 13, Injection canula. 14, A
metal dissection tray. 15, Death
chamber. 16, Base of same. 17, Rubber
tube connecting gas cock with death
chamber. 18, Bone saw. 19, Bone cutter.
20, Scapula. 21, Tenaculum. 22,
Forceps. 23, Straight scissors. 24, Small
pair of curved scissors.

A convenient dissection tray may be made from galvanized iron. It
should be 16 inches square and about 1 inch deep (Fig. 84, No. 14).
A death chamber is made by using a bell jar 12 inches in diameter at the
bottom. This is used on a perfectly smooth board 16 inches square. Through
the center of this board is inserted a glass tube ⅜ inch in diameter. To this
glass tube is attached a rubber tube the other end of which is attached to a
gas jet.

Page 394

The instruments needed in dissecting are illustrated in Fig. 84. No. 18 is a
bone saw; No. 20 is a scalpel; No. 21 is a tenaculum; No. 22 is a pair of
forceps; No. 23 is a pair of straight scissors; and No. 24 is a small pair of
curved scissors.

Page 395

BIBLIOGRAPHY
Baum and Ellenberger, Handbuch der Vergleichenden Anatomie, Berlin, 1912.
Barrows, H. R., Me. E. S. Bull. 232, pp. 16, plates 6, 1914.
Bradley, O. Charnock, The Structure of the Fowl, pp. 146, illustrations 73.
Chaveau, A., Comparative Anatomy of Domestic Animals, New York, 1893.
Curtis, M. R., Ligaments of the Oviduct of the Fowl, Me. E. S. Bull. 206, 1910.
Duval, ——, Atlas of Embryology.
Foster and Balfour, Elements of Embryology.
Gadow, H., and Selenka, E., Vögel. I. Anatomischer Theil (Dr. H. G. Bronn’s Klassen und
Ordnungen des Thier-Reichs. Sechester Band, Vierte Ahtheiburg), Leipsig, 1891.
Gray, Henry, Anatomy Descriptive and Surgical, New York, 1908.
Heisler, J. C., Embryology, Philadelphia, 1901.
Kaupp, B. F., Male Reproductive Organs of the Fowl, Am. Jr. Vet. Med., vol. x, 11, 2.
Kaupp, B. F., Female Reproductive Organs of the Fowl, Am. Vet. Rev., vol. 49, 11, 4.
Leisering Atlas of Anatomy, edited by W. Ellenberger, translated by A. T. Peters, Chicago, 1905.
Lillie, F. R., Embryology of the Chick, Chicago, 1906.
Owen, R., Comparative Anatomy and Physiology of Vertebrates, London, 1866.
Schmeisser, H. C., A Study of the Blood of Fowls, Johns Hopkins Hospital, 1915.
Shufeldt, R. W., Myology of the Raven, pp. 318, illustrations 76, London, 1890.
Strangeways’ Veterinary Anatomy, edited by I. Vaughan, Edinburgh, 1892.
Surface, F. M., Histology of the Oviduct of the Fowl, Me. E. S. Bull., 206, 1912.

Page 396

INDEX

Abdominal air-sac, 202
cavity, 156
Abducens nerve, 270
Abductor minimi digiti muscle, 110
Accessorius spinalis nerve, 274
Accessory organs of digestion, 152
Acetabulum, 48
Achillis tendon, 69
Acoustic lamina, 323
nerve, 306
vesicle, 322
Adductor longus muscle, 117
magnus muscle, 117
Adrenal gland, 191
Adventitia, 201
Afferent nerves, 300
Air-sacs, 199, 325
abdominal, 202
anterior diaphragmatic, 202
thoracic, 200
cervical, 201
femoral extensions, 203

Page 397

humeral extension, 200
posterior diaphragmatic, 202
subpectoral prolongation, 200
subscapular prolongations, 200
suprarenal extensions, 203
Alæ cinereæ, 291
orbitale, 28
temporales, 29
Albumin, 180
portion of oviduct secreting, 185
Allantois, 321
Alula, 311
Alveolar glands, 141
nerve, 270
Amnion, 320, 327
Ampullæ, 306
Ampullar dilatations, 322
Anapophyseal ridge, 38
Anatomic specimen, preparation of, 349
Anconeus muscle, 107
Angiology, 206
Angular glands, 141
groove, 52
Annular ligament, 58
Annulus fibrosus, 58
Anterior coraco-brachialis nerve, 284
diaphragmatic air-sac, 202
fossa, 25
thoracic nerve, 284
Aortic arch, 325

Page 398

bulb, 324
Aponeurosis, 59
Apparatus, circulatory, 206
digestorius, 135
respiratory, 193
uro-genitalis, 169
vocal, 195
Appendages, structure of, 309
Appendico-costales muscle, 99
Appendicular skeleton, 13
Apteria, 34
Aqueduct of Sylvius, 268, 289
Arachnoid, 288, 289
Arbor vitæ, 291
Arch, hemal, 38
scapular, 40
Area opaca, 332
pellucida, 332
vasculosa, 332
Arteria cerebri profunda, 217
Artery or arteries, 209, 325
acromial, 222
anterior circumflex humeral, 222
vertebral, 221
aorta, 211
auricular, 220
axillary, 222
basilar, 217
brachialis, 222
brachio-cephalic sinister, 212
bronchialis, 215

Page 399

carotid trunk, 215
carotis cerebralis, 215
communis, 215
externa, 215
celiac axis, 226
cerebral, 217
cerebri profunda, 217
cervicalis ascendens, 221
circumflex femoris, 228
clavicular, 222
coccygeal laterales, 232
collateralis radialis, 223
common aorta, 211
coronary, 209
crural, 228
esophageal, 224
ethmoidal, 218
ethmoidales externa, 218
external facial, 220
thoracic, 222
facial, 220
femoral 228
hemorrhoidalis intima, 232
hepatica dextra, 227
hyoid, 218
iliac, 229
inferior cerebellar, 217
esophageal, 215
thoracic, 222
intercostal, 224
internal alveolar, 220
ethmoid, 218
facial, 220
mammary, 222
maxillary, 220
ophthalmic, 217
pelvic, 228

Page 400

thoracic, 222
lacrimalis, 217
lingualis, 220
lumbar, 225
median coccygeal, 232
hemorrhoidal, 227
meningeal, 216
mesenteric, 227
muscularis, 207
occipital, 216
occipitalis profunda, 216
sublimis, 216
ophthalmica externa, 216
ovarian, 226
plexus palpebralis, 217
temporalis, 216
posterior aorta, 224
circumflex humeral, 223
mesenteric, 227
vertebral, 221
profunda communis, 231
penis, 232
pudenda externa, 232
pulmonalis dexter, 213
sinister, 213
pulmonary, 213
radial, 223
ramus anterior, 217
posterior, 217
profundus, 209
superficialis, 209
recurrent ciliaris posticus, 217
ilio-celiacus, 227
intestinalis, 227
renalis, 229
sinister, 227
superior hemorrhoidal, 227

Page 401

ulnar, 223
renal, 226
retinæ centralis, 217
sacralis media, 229, 232
spermatic, 226
sphenoid, 217
spheno-maxillaris, 217
splenic, 227
sternal, 222
sterno-clavicularis, 221
subclavian, 212
subcutaneous colli, 215
subscapular, 222
superior cervical, 215
laryngeal, 218
sylvian, 217
temporal, 216
thoracic, 222
thyroid, 215
tibialis antica, 230
postica, 230
ulnar, 223
umbilical, 228
vertebral, 215
Arthrology, 56
Articulo-jugale, 58
Arytenoid cartilage, 194
Atlas, 37
Auricle, 324
Auricular appendage, 208
meatus, 305
ossicles, 305
ventricular valve, 207
Axial skeleton, 23

Page 402

Axillaris nerve, 23
Axis, 37
cylinder process, 277
Axolemma, 277
Axone, 277
hill, 277

Barbes, 310
Barbules, 310
Basi-branchial bone, 35
Basi-hyal bone, 33, 36
Basilar artery, 217
Beak, 139, 310, 316
Biceps band, 114
brachii, 104
flexor cruris, 113
Biventer cervicis muscle, 77, 83
Blastema, 322
Blastoderm, 318
Blood, 257
coagulation, 260
composition, 260
formation, 260
function, 257
plasma, 260
reaction, 257
vascular system, 206
vessels, 209
Bloom, 188
Bone or bones, 17

Page 403

atlas, 37
axis, 37
cancellous, 18
carpus, 44, 47
classification, 20
compact, 17
composition, 21
cervical vertebræ, 35, 37
coccygeal, 35, 41
dorsal vertebræ, 35, 39
entoglossal, 35
ethmoidal, 23, 27
femur, 50
fibula, 53
flat, 21
frontal, 23, 29
furculum, 24
growth, 20
humerus, 44, 45
hyoid, 35, 36
ilium, 49
inferior maxilla, 23, 34
irregular, 21
ischium, 49
jugale, 23, 31, 33
lacrimal, 23, 31, 33
long, 20
lumbo-sacral, 35, 39
maxillæ, 23, 31, 32
metacarpus, 44, 47
metatarsus, 53
nasal, 23, 31, 32
occipital, 23, 35
of cranium, 23
of face, 31
of fore limb, 44
of hind limb, 50

Page 404

of pelvis, 48
of shoulder, 43
of skull, 23
of thorax, 42
of vertebræ, 26
palatine, 23, 31, 33
parietal, 23, 29
phalanges, 44, 47
premaxilla, 23, 31
pterygoid, 23, 31, 33
pubis, 50
pygostyle, 24
quadrate, 23, 34
quadrate-jugale, 23, 33, 36
radius, 44, 46
ribs, 41
scapular arch, 40
sesamoid, 54
sphenoid, 25, 28
supplied with air, 204
tarsus, 53
temporal, 23, 29
tibia, 52
turbinated, 34, 193
ulna, 44, 46
vomeral, 23, 31, 32
zygomatic, 23, 31, 32
Bowman’s capsule, 171
Brachial nerve plexus, 282
Brain, 288
alæ cinereæ, 291
anterior commissure, 296
aqueduct of Sylvius, 289
arbor vitæ, 291
calamus scriptorius, 290
cerebral peduncles, 291

Page 405

choroid plexus, 296
corpora restiformia, 289
corpus callosum, 296
striatum, 296
coverings, 288
crura cerebelli, 291
cerebri, 289
fore, 290
fourth ventricle, 290
hind, 290
hippocampus, 297
hypophysis, 289
inferior pyramids, 291
lamina terminales, 295
lateral ventricles, 297
medulla oblongata, 290
mid-, 290
nervi amygdales, 296
optic chiasm, 289
lobes, 289
pars commissuralis, 289
pons varolii, 289
processus cerebri mammillares, 297
pyramidal columns, 291
sulcus centralis, 291
superior pyramids, 291
thalami optici, 289
tubercula olfactoria, 297
valve of Vieussens, 290
ventricles, lateral, 297
Bronchi, 193, 197
diaphragmatic, 197
Bronchial artery, 215
tubes, 197
Bronchialis anticus, 89, 105
longus inferior nerve, 284

Page 406

superior nerve, 283
posticus, 89
Broncho-trachealis anticus, 38
brevis, 89
Brunner’s glands, 149
Bulla tympaniformis, 195
Bursa of Fabricius, 152

Cæca, 151
Calamus, 310
scriptorius, 290
Canal or canals, caroticus et jugulare, 27
Haversian, 17
hypotarsal, 53
ilio-lumbalis, 48
neural, 38
of Petit, 305
urinary, 170
Volkmann’s, 17
Canaliculi, 17
Cancelli, 17
Capillaries, 209
Capsular ligament, 57
Caput costæ, 42
Carotid trunk, 215
Carotin, 314
Carotis cerebralis artery, 215
communis, 215
externa artery, 215
Carpi radiale, 47

Page 407

ulnare, 47
Carpus, 44, 47
Cartilage semi-lunaris, 69
Cavity, cotyloid, 49
glenoid, 44
glenoidalis interna, 67
nasal, 35
sigmoid, 46
Cavum cranii, 23
ilio-lumbale dorsales, 48
Celiac axis, 226
Cera, 310
Cerato-branchial cartilage, 35
Cerato-glossus muscle, 80
Cerato-hyoideus muscle, 80
Cerebellar cortex, 293
Cerebellum, 25, 295
Cerebral lobes, 322
peduncles, 291
Cerebro-spinal axis, 288
nervous system, 265
Cerebrum, 25
Ceroma, 37
Cervical air-sac, 201
artery, superior, 215
nerve ganglion, 270
sympathetic nerve ganglion, 275
vertebræ, 35, 37
Chalazæ, 180

Page 408

Chamber, nasal, 193
Chorion, 321, 327
Choroid coat, 323
Choroidea, 303
Chromophilic bodies, 280
Chromosomes, 318
Ciliary ganglion, 271
nerve, 304
process, 304, 323
Circulatory system, 206
Circumconcha muscle, 128
Circumduction, 57
Clavicle, 44
Clavicular artery, 222
Claws, 310
Cleido-trachealis muscle, 75
Cloaca, 151
Clothing feathers, 310
Coccygeæ laterales arteries, 232
vertebræ, 33, 41
Cochlearis, 305
Collum costæ, 42
Color of skin, 314
Columella, 31, 305
Column, vertebral, 35
Columnæ carnæ, 207
Complex nerve ganglion, 271

Page 409

Complexus muscle, 81
Composition of bone, 21
of egg, 181
Condyle, external, of femur, 50
inner, of femur, 51
Conjunctiva, 303
Constrictions of Ranvier, 277
Coprodeum, 151
Coraco-brachialis muscle, 103
Coraco-humeralis muscle, 101
Coracoid bone, 194
Corium, 313
Cornea, 323
Corneum, 309
Cornu, hyoid, 35
Coronary artery, 209
Corpora restiformia, 289
Corpus ciliare, 303
Costal bronchial tubes, 197
process of sternum, 24
Cotyloid cavity, 65
Course of food, 152
Cranial cavity, 23
Cranium, 23
Cricoid, 194
Crico-trachealis ligament, 194
Cristiilii, 48

Page 410

sterni, 42
Crop, 142
Crura cerebelli, 291
cerebri, 289
Crural artery, 228
nerve plexus, 283
Crystalline lens, 303, 304, 303, 322, 323
Cuneiform bone, 46
Cutaneous brachii superior nerve, 283
follicle, 323
Cutis, 313

Deglutition, 143
Deltoid, 104
Dendrites, 297
Depressor caudæ muscle, 95
coccygis muscle, 95
glossus muscle, 80
palpebræ inferioris, 125
Derivatives of germ layer, 342
Dermis, 313
Dermo-cleido dorsalis, 75
Dermo-dorsalis, 72
Dermo-frontalis, 72
Dermo-humeralis, 72
Dermo-iliacus, 75
Dermo-pectoralis, 73
Dermo-spinalis, 75

Page 411

Dermo-temporalis, 73
Dermo-tensor patagii, 72
Dermo-ulnaris, 76
Diaphragm, 165
Diaphragmatic bronchial tubes, 197
Diapophysis, 38
Digastric muscle, 78
Digestive apparatus, 135
Digits, 54
Dissection, 343
laboratory, 351
of arteries, 345
of bone, 346
of muscles, 343
of nerves, 347
of viscera, 344
Division of skeleton, 22
Dorsal ligament of oviduct, 188
vertebræ, 35
Dorso-cutaneous nerve plexus, 283
Ductless glands, 148, 329
adrenal, 191
parathyroid, 191
spleen, 155
thymus, 190
Ductus arteriosus, 325, 329
Botalli, 214
Duodenum, 148, 150
Dura mater, 288

Page 412

Ear labyrinth, 305
Ectoderm, 320
Efferent nerves, 300
Egg, 180
composition, 181
tooth, 327
Embryology, 318
Endocardium, 206, 207, 208
Endolymph, 306
Endothelium, 206
Entoderm, 320
Entoglossal bone, 35
Entotympanic, 77
Epicondyloid fossa, 52
Epidermis, 176, 207, 313
Epididymis, 176
Epineural appendage, 38
Equipment, 351
Erythrocytes, 258
fate of, 261
Esophageal artery, 224
inferior, 215
Esophagus, 142
Esthesiology, 303
Ethmoid bone, 27
Eustachian tube, 29, 136
Extensor annularis brevis muscle, 121
brevis digitorum muscle, 120

Page 413

digitorum communis muscle, 106
femoris muscle, 113
hallucis brevis muscle, 119
indicis longus muscle, 108
longus digitorum muscle, 119
metacarpi radialis longior muscle, 105
ossis metacarpi pollicis muscle, 107
proprius pollicis muscle, 109
External facial artery, 220
thoracic artery, 222
Extremitas vertebralis, 42

Fabricius, bursa of, 152
Facial artery, 220
Falx cerebri, 289
Fasciculi, 70, 71
deep, 71
superficialis, 71
Feathers, 311
alula, 311
coverts, 311
primaries, 311
rectrices, 311
rudder, 41
scapularies, 311
secondaries, 311
tertiaries, 311
Female generative organs, 178
Femoral artery, 228
Femoro-caudal, 114
Fenestra ovalis, 31
rotunda, 31

Page 414

vestibularis, 105
Fertilization, 318, 319
Fetal circulation, 329
Fibers of Sharpey, 20
Fibrin ferment, 261
formation, 261
Fibrinogen, 261
Fibrino-globulin, 261
Fibular bone, 53
ridge, 52
Fifth cranial nerve, 268
inferior maxillary division, 268
ophthalmic division, 268
superior maxillary division, 268
Filiform papillæ, 41
Filo-plume, 311
Flesh, 70
Flexor brevis pollicis muscle, 109
capitis inferior muscle, 82
carpi ulnaris brevior muscle, 109
muscle, 108
digitorum profundus muscle, 108
sublimis muscle, 108
hallucis brevis muscle, 121
longus muscle, 122
metacarpi brevis muscle, 111
radialis muscle, 106
minimi digiti muscle, 110
brevis muscle, 110
perforans digitorum profundus muscle, 124
perforatus annularis primus pedis muscle, 122
indicis primus pedis, 123

Page 415

medius primus pedis, 123
secundus pedis, 121, 122
Fontanel, 27
Foramen intervertebralis, 39
ischiadic, 24, 49
magnum, 23
Monro, 295
nutrient, 52
oblongum, 24
optic, 27
ovale, 306, 207, 329
pneumatic, 42, 43, 45
triossium, 44, 61
Fore brain, 290
limb, 44
Fossa anterior, 25
articularis transversa, 54
cranii media, 25
posterior, 25
epicondyloid, 52
epitrochlear, 51
intercondyloid, 51
middle, 25
ovalis, 207
pneumatic, 45
posterior, 25
subcondyloid, 27
trochanteric, 50
Fourth ventricle, 290
Fovea cardiaca, 324
ischiadica, 48
lumbalis, 48
pudendalis, 48
Fowl skeleton, 21

Page 416

Frontal bone, 29
Function, centers of, 301
muscles of, 128
Funnel portion of oviduct, 183
Furculum bone, 24

Gall-bladder, 154
Ganglion, 300
cardiacum, 299
cervical, 270
sympathetic, 275
ciliary, 271
complex, 271
Gasserian, 268
geniculate, 271
inferior cervical, 299
orbito-nasal, 270
petrosal, 272
spheno-palatine, 270
spinal, 276
structure of, 277
superior cervical, 299
sympathetic, 272
thoracic, 299
vagi radicis, 272
Gastrocnemius muscle, 117
Gemellus muscle, 116
Genio-hyoideus muscle, 79
Genital system, 169
Germ layer, 342
Gland, alveolar, 141
angular, 141

Page 417

ductless, 190
lacrimal, 303
meibomian, 303
mouth, 141
mucous, 136
oil, 41
pharynx, 141
sublingual, 141
thymus, 190
thyroid, 190
uropygii, 309
Glosso-hyal element, 35
Glottis, 194
Gluteus medius muscle, 112
minimus muscle, 112
primus muscle, 112
profundus muscle, 112
Gray matter of cord, 292
Groove, angular, 52
tendonal, 54
Growth of bone, 20

Hallux, 54
Hand, 47
Hard palates, 136, 139
Haversian canals, 17
Heart, 206
structure of, 207
ventricles of, 324
Hemal arch, 38
Hemapophysis, 38

Page 418

Hemophage, 262
Hemorrhoidalis intima artery, 232
Henle’s limb, 171
loop, 171
Hepar, 153
Herbst’s corpuscles, 307
Hind brain, 290
limb, 50
Hormone, 190
Humerus, 44, 45
Hyoid, 218
arch, 324
bone, 35
Hyoideus transversus muscle, 80
Hypapophysis, 38
Hypocleidum, 24, 44
Hypoglossal nerve, 274
Hypophysis, 289, 295
Hyporachis, 313
Hypotarsal canal, 53
Hypotarsus, 53

Ilio-lumbalis dorsalis, 48
Ilium bone, 49
Immovable joints, 56
Inferior alveolar artery, 220
cerebellar artery, 217
larynx, 193

Page 419

maxillary bone, 34
pyramids, 291
thoracic artery, 222
tuberculum ossis carpi radialis, 47
Infracoccygis muscle, 96
Infraorbital sinus, 32
Ingluvies, 142
Inner ear, 306
Interarticulares muscles, 85
Intercostal arteries, 224
nerve, 285
Intercostales muscles, 98
Internal adhesio cornu antici cartilaginis lunatæ, 67
ethmoidal artery, 218
facial artery, 220
mammary artery, 222
mandibular vein, 237
maxillary artery, 220
ophthalmic artery, 217, 218
pelvic artery, 228
secretion, 190
thoracic artery, 222
Interosseous ligament, 58
Interosseus dorsalis muscle, 110
palmaris muscle, 111
Interspinales muscles, 85
Intertransversales muscles, 86
Intestine, free portion, 150
large, 150
small, 147
Intestinum tenue, 147

Page 420

Iris, 323, 303, 304
Ischiadic artery, 229
foramen, 49
nerve, 286
Ischium, 49
Isthmus, 186

Joints, 56
immovable, 56
mixed, 56
movements, 56
Jugal bone, 23, 31, 33
Jugular vein, 233

Kerato-hyalin, 314
Kerato-hyoideus muscle, 80
Kidneys, 169

Lacrimal bone, 23, 31, 33
duct, 303
gland, 303
sac, 303
Lacunæ, 17
Lamellæ, 17
circumferential, 17
concentric, 17
interstitial, 17
Lamina perpendicularis, 28
Laminæ terminale, 29
Langerhans, islands of, 303

Page 421

Large intestine, 150
Larynx, 141
bronchio-trachealis, 194
false, 194
inferior, 193
superior, 193
true, 194
Lateral process, 38
Lateralis caudæ muscle, 95
coccygeus muscle, 95
Latissimus dorsi muscle, 96
nerve plexus, 282
Leucocytes, 258
basophile, 259
eosinophile, 258
lymphocyte, 259
mast cell, 259
mononuclear, 259
polymorphonuclear, 258
Levator caudæ muscle, 93
coccygis muscle, 93
palpebræ superioris muscle, 124
scapulæ muscle, 103
Levatores costarum muscle, 98
Lien, 155
Ligament or ligaments, 57
annular, 58
annulare radii, 61
anterior cruciatimi genu, 69
anterius ossis carpi metacarpi et primæ, 69
phalangis digiti secundi, 64
patellar, 67
antero-inferior humero-coracoideum, 61

Page 422

anticum, 69
articulo-jugale, 58
capsular, 57
capsulare atlantico-epistrophicum odontoideum, 59
atlantico-occipitale, 58
capituli fibulæ, 68
cubiti, 61
digitorum pedis, 69
obliquum, 59
ossis tibio-metatarsi, 69
carpi interosseum, 64
radialis internum, 64
claviculosternal, 44
coraco-furculare, 61
coraco-humeralis, 61
coraco-scapulare, 61
inferius, 61
internum, 61
crico-trachealis, 194
cubiti teres, 62
elasticum interspinale profundum, 59
superficiale, 59
externum, 69
extero-laterale genu, 65
furculo-scapulare, 61
humero-scapulare, 61
ilio-pubic, 65
ilio-sacrale, 65
inferius, 61
internum, 64
intero-laterale genu, 66
interosseous, 58
interosseum, 69
intervertebral, 38
laterale cubiti externum, 61
internum, 61
nuchæ, 59

Page 423

obliquo-carpi ulnaris, 62
of carpal joint, 61
of ear, 58
of elbow-joint, 59
of finger, 64
of hip-joint, 65
of jaws, 58
of knee-joint, 65
of liver, 153
of oviduct, 188
of pelvis, 56
of ribs, 59
of shoulder-joint, 59
of sternum, 59
of tibio-metatarsal joint, 69
of toes, 69
of vertebræ, 58
ossis carpi radialis internum et metacarpi, 64
ulnaris externum et metacarpi, 64
internum et metacarpi, 64
pollicare, 64
popliteum, 67
posterior cruciatum genu, 67
posterius, 64
posticum ulnare carpi ulnaris, 63
Poupartii, 65
radiale carpi radialis externum, 64
structure, 57
superius, 69
suspensorium corporum vertebralium, 58
suspensorium dentis epistrophei, 58
tibio-fibulare, 68
transversale commune, 67
transversum, 59
atlantis, 58, 59
externum, 59
triangulare, 59

Page 424

ulnare carpi radialis, 63
internum, 63
metacarpi externum, 64
internum, 64
Limb, fore, 44
hind, 50
Lingua, 139
Linguales arteries, 220
Lipochrome, 314
Liquor pericardii, 207
sanguinis, 258
Liver, 152, 153
ducts, 155
Longissimus capitis et atlantis, 85
dorsi, 92
Longus colli dorsalis muscle, 83
muscle, 83
posticus muscle, 83
Lumbar arteries, 225
Lumbo-sacral vertebræ, 35, 39
Lumbo-sacrales nerves, 285
Lung, 195, 325
tubules, 197, 199
primaries, 197
secondaries, 198
tertiaries, 198
Lymph vascular system, 206, 254
Lymphocytes, 259

Malaris muscle, 125

Page 425

Male generative organs, 175
Malpighian body, 155, 156, 171
Mandibular arch, 324
Marrow, 20
red, 20
yellow, 20
Masseter muscle, 77
Mast cells, 259
Maxilla, 23, 31, 32
Maxillary arch, 324
Median coccygeal artery, 323
hemorrhoidal artery, 227
nerve, 284
Medulla oblongata, 25, 290
ossium flava, 20
rubrum, 20
Meibomian glands, 303
Melanin, 316
Membrana nictitans, 303, 324
putaminæ, 329
semi-lunaris, 195
testacea, 187
tympana interna, 195
Membranæ obturatoræ intervertebrales posteriores, 59
Meningeal artery, 216
Meninges, 288
Meniscus, 56
intervertebralis, 58
Mesentery, 156, 157

Page 426

Metacarpus, 44, 47
Metasternum, 42
Mid brain, 290
Middle fossa of cranium, 25
meningeal artery, 217
Molting, 313
Motor oculi, 267
Mouth, 135
Movable joints, 56
Mucous glands, 136
Müllerian duct, 184
Muscle or muscles, 70
abductor minimi digiti, 110
adductor longus, 117
magnus, 117
anconeus, 107
biceps, 104
flexor crurus, 113
biventer cervicis, 83
maxillæ, 77
brachialis anticus, 105
bronchialis anticus, 89
posticus, 89
broncho-trachealis anticus, 88
brevis, 89
posticus, 89
cerato-glossus, 80
cerato-hyoideus, 80
ciliary, 304
cleido-trachealis, 75
complexus, 81
constrictor glottidis, 87
coraco-brachialis, 102

Page 427

coraco-humeralis, 101
deltoid, 104
depressor caudæ, 95
coccygis, 95
glossus, 80
dermal, 70, 71
dermo-cleido-dorsalis, 75
dermo-dorsalis, 72
dermo-frontalis, 72
dermo-humeralis, 72
dermo-iliacus, 75
dermo-osseous, 70, 73
dermo-pectoralis, 73
dermo-spinalis, 75
dermo-temporalis, 73
dermo-tensor patagii, 72
dermo-ulnaris, 76
diaphragm, 90
digastricus, 78
entotympanic, 77
expansor secundarium, 62
extensor digitorum communis, 106
femoris, 113
indicis longus, 108
metacarpi radialis longior, 105
ossis metacarpi pollicis, 107
proprius pollicis, 107
femoro-caudal, 114
flexor brevis pollicis, 109
capitis inferior, 82
carpi ulnaris, 108
brevior, 109
digitorum sublimis, 108
metacarpi brevis, 111
radialis, 106
minimi digiti, 110
brevis, 110

Page 428

profundus, 108
gastrocnemius, 117
gemellus, 116
genio-hyoideus, 79
gluteus maximus, 50
medius, 112
gluteus minimus, 112
primus, 112
heart, 71
hyoideus transversus, 80
infracoccygis, 96
interarticulares, 85
internal obturator, 49
interosseus dorsalis, 110
palmaris, 111
interspinales, 85
intertransversales, 86
involuntary, 70
striated, 71
lateralis caudæ, 95
coccygis, 95
latissimus dorsi, 96
levator caudæ, 93
coccygis, 93
scapulæ, 103
levatores costarum, 98
longissimus dorsi, 92
longus colli anticus, 84
posticus, 83
masseter, 77
mylo-hyoides, 79
nomenclature, 71
obliquo-transversales, 82
obliquus abdominis externus, 90
internus, 91
colli, 83
obturator externus, 116

Page 429

internus, 116
of abdomen, 90
of air passage, 86
of anterior pectoral region, 99
of brachial region, 104
of cervical region, 81
of coccygeal region, 93
of costal region, 96
of digit, 109
of dorso-lumbar region, 92
of forearm and hand, 105
of head, 76
of inferior larynx, 86
of pectoral region, 100
of posterior limb, 111
of scapular region, 101
of sternum, 90
of superior larynx, 86
of tibial region, 117
of tongue, 79
pectoralis major, 100
secundus, 100
tertius, 100
peroneus longus, 118
platysma myoides, 74
pronator brevis, 107
longus, 107
pterygoideus externus, 78
internus, 78
lateralis, 78
medius, 74
rectus abdominis, 91
capitis anticus minor, 81
lateralis, 84
posticus major, 82
rhomboideus, 17
sacro-lumbalis, 92

Page 430

sartorius, 111
scalenus medius, 86
scapulo-humeralis, 101
semimembranosus, 114
semitendinosus, 114
accessorius, 114
serratus magnus anticus, 97
parvus anticus, 97
skeletal, 70, 76
soleus, 118
sphincter, pupillary, 304
sterno-trachealis, 89
stylo-hyoideus, 79
subclavius, 102
subscapularis, 103
supraspinatus, 102
temporal, 76
tensor patagii brevis, 99
longus, 99
teres et infraspinatus, 98
minor, 102
thoraco-scapularis, 103
thyreo-arytenoideus, 85
trachelo-mastoideus, 85
tracheo-lateralis, 87
transversalis abdominis, 90
transversus peronei, 94
trapezius, 97
triceps, 104
true dermal, 71
voluntary-striated, 70
Myelon, 322
Myeloncephalus columns, 320
Myocardium, 208

Page 431

Nails, 316
Nasal bone, 23, 31, 32
cavity, 35
chambers, 193
Naso-premaxillary process, 324
Nerve or nerves, 264
abducens, 70
accessorius spinalis, 274
acoustic, 271
afferent, 300
alveolar, 270
anterior coraco-brachialis, 284
spinal branches, 281
thoracic, 284
axillaris, 283
brachial plexus, 282
brachialis longus inferior, 284
superior, 283
cells, 280
centers, 30
ciliary, 304
cranial, 265
crural plexus, 285
cutaneous brachialis et inferior brachialis, 284
brachii superior, 283
dorsal spinal, 281
dorsalis plexus, 282
dorso-cutaneous plexus, 283
efferent, 300
ethmoidalis, 269
facialis, 286
function, 300, 301
furcularis, 286
glosso-pharyngeal, 272
hypoglossal, 27, 37, 274
intercostal, 285

Page 432

ischiadic, 49, 286
latissimus dorsi, 282
lumbo-sacral, 285
median, 284
medullated, 277
motor oculi, 267
neurolemma, 277
non-medullated, 277
obturator, 286
olfactorius, 34, 265
optic, 267
patheticus, 268
peroneus profundus, 287
plexus pedundus, 288
pneumogastric, 273
posterior coraco-brachialis, 284
ramus secundus, 269
recurrent cardiacus, 274
externa, 269
hepatici, 274
infra-orbitale, 269
laryngeus, 274
linguales, 273
pharyngeus, 272
pulmonale, 274
subcutaneous, 270
ventralis, 281
rhomboideus profundus, 282
superficialis, 282
scapulo-humeralis, 282
serratus plexus, 282
spinal cord, 275
sterno-coracoideus, 284
subcoraco-scapularis, 282
superficialis peroneus, 287
serratus, 282
supra-coracoideus, 283

Page 433

trifacial, 31, 268
ulnar, 284
vagus, 27, 31, 273
group, 273
Nerve trunks, structure of, 277
Nervous system, 264, 300
Neural arch, 38
spines, 38, 39
Neurofibrils, 280
Neurones, 268, 279
Nostril, 193
Notocord, 322

Oblique process, 39
Obliquo-transversales muscle, 86
Obliquus abdominis externus muscle, 90
internus muscle, 91
dorsalis, 125
inferior, 127
superior, 125
ventralis muscle, 121
Obturator externus, 116
internus, 116
nerve, 286
Occipital artery, 215
bone, 23, 25
Occipitale laterales bone, 25
Occipitalis inferius bone, 25
profunda artery, 215
sublimis artery, 215
superioris bone, 25

Page 434

Odontoid process, 37
Oil gland, 41
Olecranon, 46
Olfactory cavities, 322
cerebral crura, 295
glomeruli, 265
nerve, 265
Oögenesis, 319
Ophthalmic vesicle, 322
Ophthalmica externa, 216
Optic chiasm, 289
lobes, 322, 289
nerve, 267
Orbicularis oculi, 124
palpebrarum muscle, 124
Orbit, 323
Orbital process, 30
Orbito-nasal ganglion, 270
Organ of hearing, 304, 322
of sight, 303
of smell, 307
of taste, 307
of touch, 307
Os angulare, 30
articulare, 30
transversale, 105
Osseous structure, 17
tissue, 17
Ostium tubæ abdominale, 183
Otocrane, 323

Page 435

Otoliths, 322
Ovarian artery, 226
pocket, 189
Ovary, 325
Oviduct, 182, 325
Ovum, 318

Palatal papillaries, 141
Palatine glands, 141
Palatinus bone, 23, 31, 33
Palatum durum, 139
Palpebral plexus, 217
Pancreas, 152, 155
Papilla, 141
Parapophysis, 38
Parietal bone, 29
Pars commissuralis, 289
glandularis, 143
muscularis, 143
renalis, 251
Partes pedunculares, 294
Patella, 53
Patheticus, 268
Pecten, 303, 323
Pectoralis major, 100
secundus, 100
tertius, 101
Pelvic cavity, 156

Page 436

girdle, 48
Pericardium, 207
Perimysium, 70
Periosteum, 18
Peritoneum, 156
Peroneus longus, 118
nerve, 287
Pessulus, 195
Petrosal ganglion, 272
Phalanges, 44, 47, 54
Pharynx, 54, 141
Pia mater, 288
Pineal gland, 295
Pituitary body, 25, 289, 295
Placenta, 321
Planum coccygeum, 48
Plasma, 261
Platysma myoides muscle, 74
Pleurapophysis, 38
Plexus, abdominal, 299
anterior splanchnic, 300
Plexus, lacrimal, 217
mesenteric, 299
muscularis, 217
pedundus, 288
posterior splanchnic, 300
thoracic, 299
Plica primitivæ, 320

Page 437

Pneumatic foramen, 42, 43, 45
Pons varolii, 289
Post-acetabular ridge, 48
Posterior aorta, 224
circumflex artery, 223
diaphragmatic air-sac, 202
fossa, 25
nares, 136
orbitalis, 30
vena cava, 247
vertebral artery, 221
vein, 234
Poupart’s ligament, 65
Prezygapophyses, 39
Primaries, 311
Primitive streak, 321
Process, costal, 43
lateral, 37, 39
oblique, 37, 39
of sternum, 42
odontoid, 37
xiphoid, 43
Processus acusticus externus, 31
ciliaris, 304
coracoideus, 44
cubitalis humeri, 45
frontalis, 32
anterior, 32
posterior, 32
furcularis, 43
humeralis, 43
intermaxillaris, 32
ischiadicus, 49

Page 438

maxillaris, 32
anterior, 32
odontoid, 37
olecranalis coracoideus, 46
orbicularis, 28, 29
orbitalis, 29
palatinus, 32
posterior orbitalis, 30
Processus uncinatus, 24
zygomaticus, 28, 30
Profunda penis, 232
Pronation, 57
Pronator brevis muscle, 107
longus, 107
Proteids of plasma, 261
of serum, 261
Proventriculus, 143
Provertebra, 320
Pterygoideus externus muscle, 78
internus muscle, 78
lateralis muscle, 78
medialis muscle, 78
Pterylæ, 311
Pubis, 50
Pudenda externa artery, 232
Pulmonalis dextra, 213
sinistra, 213
Pulmonary artery, 213
vein, 233
Pulp, 311
Punctum saliens, 320

Page 439

Purkinje cells, 293
Pyramidal columns, 291

Quadrate, 34
Quadrato-jugale, 23, 31, 33
Quadratus nictitans, 125
Quill, 310
feathers, 310

Rachis, 310, 313
Radial artery, 223
Radius, 44, 46
Rami communicantes, 276
glottis, 194
Ramus ascendens ossis ischii, 49
ciliaris posticus, 217
posterior artery, 217
profundus artery, 209
superficialis artery, 209
Rectrices, 41, 311
Rectus abdominalis muscle, 91
capitis anticus minor muscle, 81
dorsalis major muscle, 82
posticus major muscle, 82
Rectus capitis ventralis muscle, 82
dorsalis muscle, 127
externus muscle, 127
inferior muscle, 127
internus muscle, 128
lateralis muscle, 127
medialis muscle, 128

Page 440

superior muscle, 127
ventralis muscle, 127
Recurrent cardiacus nerve, 274
hepatici nerve, 274
infraorbital nerve, 269
intestinalis nerve, 227
laryngeus nerve, 273
lingualis nerve, 273
pharyngeus nerve, 272
pulmonale nerve, 274
renal artery, 223
renales nerves, 229
sinister artery, 227
subcutaneous nerve, 270
Red blood cells, 258
shape, 258
size, 259
structure, 259
Reflex action, 301
Renal artery, 226
corpuscle, 171
Respiratory apparatus, 193
Rete malpighii, 313
Retina, 303, 304, 323
Rhomboideus muscle, 97
profundus nerve, 282
superficialis nerve, 282
Ribs, 41
false, 41
true, 41
Ridge, ectonemial, 52
fibrillar, 52
post-acetabular, 48

Page 441

procnemial, 52
trochanteric, 50
Rotation, 57
Round ligament, 65
Rudder feathers, 41

Sacralis media artery, 229, 232
Sacro-lumbalis muscle, 92
Sacs, air, 199
Sarcolemma, 70
Sartorius muscle, 111
Scala tympani, 306
vestibuli, 306
Scalenus medius muscle, 86
muscle, 86
Scapho-lunar bone, 47
Scapula, 43
Scapulo-humeralis muscle, 101
nerve plexus, 282
Sclerotic coat, 303, 304
Secondaries, 311
Secretion, internal, 190
Semilunar cartilage, 67
Semimembranosus muscle, 114
Seminiferous tubules, 318
Semitendinosus muscle, 114
accessorius muscle, 114
Sense of hearing, 305

Page 442

of sight, 303
of smell, 307
of taste, 307
of touch, 307
organ, 303
Sensory nerves, 300
Septum nasi, 33
Serous cavity, 156
membrane, 156
sac, 156
Serratus magnus anticus muscle, 97
nerve plexus, 282
parvus anticus muscle, 97
Serum, 261
albumin, 261
globulin, 261
Sesamoid bone, 54
Sharpey’s fibers, 20
Sheath of Schwann, 277
Shell bloom, 188
gland, 187
membrane, 181
structure, 181
tint, 181
Shoulder girdle, 43
Sinus foraminis occipitales, 240
foveæ hemispherii cerebelli, 241
infraorbitalis, 32
Sinus longitudinalis, 239
occipitalis, 240
externus, 240
petrosus sphenoideus, 240

Page 443

rhomboideus, 276
semicircularis, 240
temporales, 332
temporo-sphenoideus, 240
transversus, 240
venosus annularis basilaris, 240
Skeleton, 21, 24
appendicular, 43
axial, 22
division, 22
Skin, 309, 323
Small intestine, 147
Smooth muscle, 70
Soleus muscle, 118
Somatic cell, 318
Spermatic artery, 226
Spermatids, 318
Spermatocyte, 318
Spermatogenesis, 318
Spermatogonia, 318
Spermatozoa, 176, 318
Sphenoid artery, 217
bone, 28
rostrum, 29
Spheno-maxillary artery, 217
Spheno-palatine nerve ganglion, 270
Spinal cord, 38
nerves, 281
nervous system, 264
Splanchnology, 135

Page 444

Splanchnopleure, 327
Spleen, 152, 155
Splenic artery, 227
capsule, 155
pulp, 155
Spur, 54, 317
Squamous epithelium, 137
Sternal artery, 222
Sterno-clavicularis artery, 221
muscle, 284
Sterno-coracoideus nerve, 284
Sterno-hyoideus muscle, 80
Sterno-trachealis muscle, 89
Sternum, 42
Stigmen, 179
Stomach, 143
Stratum corneum, 141, 313, 314
germinativum, 314
granulosum, 314
lucidum, 344
Malpighii, 314
Stylo-hyoideus muscle, 79
Styloid process of ulna, 46
Subclavian artery, 234
Subcondyloid fossa, 27
Subcoraco-scapularis nerve, 282
Subcutis, 309
Subscapularis artery, 222

Page 445

Succus entericus, 152
Sulcus ilio-lumbalis dorsalis, 48
centralis, 291, 294
longitudinalis, 291
Superficialis peroneus nerve, 287
serratus nerve, 282
Superior laryngeal artery, 218
larynx, 193
median fissure of cord, 276
pyramidalis, 291
sympathetic ganglion, 272
tuberculum ossis carpi radialis, 47
Supra-coracoideus nerve, 283
Sylvian artery, 217
Sympathetic caroticus cephalicus, 298
nervous system, 264, 297
ophthalmic plexus, 298
recurrent cardiacus, 299
temporo-lacrimalis, 298
thoracic trunk, 299
Symphysis ilio-sacralis, 49
ilio-sacri, 49
Synovial apparatus, 57, 156

Tarso-metatarsus, 53
Tears, 303
Temporal arterial plexus, 216
artery, 215
bone, 29
petrosal portion, 31
squamous portion, 30
Temporalis muscle, 76

Page 446

Tendon Achillis, 69
Tendonal groove, 54
Tensor patagii brevis, 99
longus, 99
tympani, 128
Teres et infraspinatus muscle, 98
minor muscle, 103
Testicles, 175
Thalamus optici, 289
Thorax, 41
Thymus gland, 190
Thyroid artery, 215
gland, 190
Tibialis anticus muscle, 119
Tissue, osseous, 17
Toes, 54
Tongue, 139, 140
Touch corpuscle, 307
Trachea, 194
Trachelo-mastoideus muscle, 85
Transparent specimens, 350
Transversales abdominis muscle, 92
Transverse fissure, 289
vein, 233
Transversus peronei, 94
Trapezius muscle, 97
Triangularis sterni muscle, 90
Triceps brachii, 104

Page 447

muscle, 104
Trifacial nerve, 268
Trochanter, 50
Trochanteric fossa, 50
ridge, 50
Trochlea, femoral, 50
True joints, 56
Tuba auditiva, 29, 136
Tuber cinereum et infundibulum, 289
Tuberculum costæ, 42
Tuberositas furcularis, 44
humeralis, 44
muscularis, 64
radii, 46
scapularis, 44
Tubuli seminiferi, 176, 318
uriniferi corticales, 170
Tunica adventitia, 210
intima, 210
media, 210
Turbinate bones, 34, 193
Tympanic membrane, 31

Ulna, 44, 46
Ulnar nerve, 284
Umbilical artery, 228
Umbilicus, 31
Ureter, 174, 187
Urinary apparatus, 169

Page 448

canals, 170
Urodeum, 151
Urogenital system, 169
Uro-hyal process, 35

Vagina, 187
Valve of Vieussens, 290
Valves of veins, 211
Vane, 310
Vas deferens, 175, 178
Vasa vasorum, 211
Vastus externus muscle, 113
internus muscle, 113
Vaxillum, 310
Vein or veins, 233
anterior vertebral, 234
ascendentes laterales, 242
basilica, 246
brachialis, 246
carotes, 241
cava sinister, 245
cavæ, 233
cephalica posterior, 239
coccygea, 230
colli cutineæ, 242
coracoidea, 244
cutinea abdominis femoralis, 250
caudalis, 251
cruralis, 249
pubica, 251
epigastric, 230
esophageal, 243

Page 449

facialis communis, 238
cutinea, 238
externa, 235
femoralis anterior, 250
interna profunda, 230
foraminis occipitalis, 240
fovæ hemispherii cerebelli, 241
glandularum thyroidearum, 243
humeri, 245
hypogastric, 251
intercostales, 244
internal mandibular, 237
intervertebrales lumbalis, 252
sacrales, 249
ischiadic, 252
jugularis, 233
linguales, 242
lingualis et hyoides, 238
longitudinalis, 239
maxillaris, 235
metatarsalis dorsalis interna, 249
profunda, 249
externa, 249
plantaris profunda, 249
occipitalis, 240
externa, 242
externus, 240
of brain cavity, 241
of dorsal region, 243
of fore limb, 245
of head, 235
of hind limb, 248
of neck, 242
of thorax, 244
of viscera, 252
ophthalmica, 236
ovariana, 252

Page 450

palpebralis, 238
petrosus sphenoideus, 240
pharyngeæ superiores, 238
poplitealis, 251
posterior vena cava, 247
vertebral, 234
profundus ulnaris, 245
proventricularis communis, 245
inferior, 253
pudenda, 251
pulmonary, 233
radialis profunda, 245
renales, 249
renalis magna, 252
retis mirabilis temporalis, 237
sacrales, 249
semicircularis, 240
spermatica, 251
sternalis, 244
structure of, 211
subclavicularis, 233
subscapularis, 243
supra-palatina, 236
suprarenalis externa, 251
revehentes, 252
surales, 244
temporalis, 238
temporo-sphenoideus, 240
testiculæ, 252
thoracica externa, 244
interna, 244
tibialis postica, 248
trachealis, 243
transversus, 233, 238
vertebralis lateralis dorsalis, 243
Venous sinuses, 239
trunks, 233

Page 451

Ventral ligament of oviduct, 188
Ventricles of heart, 324
Ventriculus, 143
Vertebræ, 35
cervical, 35
coccygeal, 35
dorsal, 35, 39
lumbo-sacral, 35, 39
Vertebral artery, 215
column, 35
Vestibulum, 306
Villi, 149
Vitellicle, 321
Vitelline membrane, 180
veins, 324, 327
Vocal apparatus, 195

Wish bone, 244
Wolffian duct, 184, 339

Xanthophyll, 314

Yolk, 180
sac, 327

Zona opaca, 320
pellucida, 320
Zygapophyses, 38, 39
Zygomatic bone, 23, 31, 33

Page 452

process, 30

Page 453

Page 454

TRANSCRIBER’S NOTES
1. Silently corrected obvious typographical errors and variations in
spelling.
2. Retained archaic, non-standard, and uncertain spellings as printed.

Page 455

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