SECTION XIII

THE CENTRAL NERVOUS SYSTEM AND THE SPECIAL SENSES

Diseases of this system and its specialized end organs of sense in the

eye, ear and nose are recognized by veterinarians as occurring among

domesticated animals, in which however they are by no means so common as

in human beings. Because of the natural reserve of wild beasts and

because their habits and manners are not so familiar to the observer, it

would seem that clinical evidences of disease of the nervous system are

rarest among them. The brain, cord and nerves of our specimens have not

been studied with the minuteness accorded to the examination of other

viscera since we have not had the personnel to devote the time to this

really colossal undertaking, our work with these tissues being directed

toward the accumulation and preservation of apparently normal brains

from every species; there are now some nine hundred brains on the

shelves. However, whenever the history of the animal before death has

suggested that disturbance in the nerve organs might exist, they have

been dissected grossly and examined microscopically. Had we subjected

all our material to microscopic study it is quite possible that we might

have discovered more lesions. This is still possible by reason of our

gross material and autopsy protocols.

We have been fortunate in having Dr. W. B. Cadwalader, Secretary of the

Society, and Dr. J. H. W. Rhein with their broad experience in

neurology, take interest in this phase of the subject and study our

material. The number of cases in which definite lesions have been found

is surprisingly small, so that no generalizations can be attempted

except perhaps in a negative sense. After the study of thirty-nine

brains and cords from animals in whose history some suggestion of

nervous system disease existed, Doctor Cadwalader could find

abnormalities in only twenty-two cases, mostly however of a very

indefinite character. This observer further points out that in his

experience with our material, his observations of our animals and a

review of the literature, he is unable to find satisfactory instances of

the so-called system or tract diseases such as tabes and lateral

sclerosis. This he suggests is due to the absence of arterial sclerosis

in the lower types of brain, intimating further that perhaps the

relation of syphilis to human arteriosclerosis and degenerative nervous

system disease is thereby strengthened. These facts being true it is not

astonishing that massive cerebral apoplexy and cerebral softening do not

occur[56]. The lesions that have been found were either definitely

infectious, as encephalitis or acute septicemia, tuberculosis,

poliomyelitis, meningitis, or the minute hemorrhages and vague

granularities or vacuolizations of nerve cells in toxemic conditions.

The material being limited and broad statements being impossible, the

important cases will be cited individually or in small groups.

CONVULSIONS.

Before entering upon the special subjects, a word might be added

concerning the clinical evidences of neurologic conditions as seen in

the Garden. Perhaps the most common and certainly the most definite

clinical sign of nervous disturbance is the convulsion. General spasms

or fits are fairly common among the carnivores and monkeys, in the

former most often associated with intestinal parasitism, in the latter

with no especial relationship unless it be renal disease. The

convulsions have been general, with and without the preservation of

consciousness. No cases of focal or Jacksonian spasms are recorded

although we shall cite two instances of tuberculoma reasonably near the

motor area in the cerebrum. The exact cause of many cases cannot be set

down since intracranial disease does not often exist.

Intoxication from chemical products of disturbed digestion or from worms

themselves is the usual explanation of spasms associated with intestinal

parasitism; if this be true, intoxication in the absence of demonstrable

parasites may also be the cause in certain cases of enteritis. However

we have seen fits when enteritis, parasites and renal disease were not

found. If these were true epilepsy, they are instances of perhaps the

rarest disease of animals, which I do not presume to diagnose.

Convulsive seizures in herbivorous animals are exceedingly rare although

I have seen clonic movements of a spasmodic character in antelopes and

deer shortly before death from gastroenteritis. Ataxia and

incoördination are much more common. Birds, notably parrots and soft-

billed insectivorous varieties, are not uncommonly afflicted with fits

but as they are rarely observed except by the keeper the exact nature is

difficult to describe. Those seen by the writer have been of two kinds.

The first and more common consists of falling from the perch in a dazed

and stiff condition, with dilated fixed eyes, stiffened and spread-out

legs and wings. Recovery follows shortly and the bird resumes its perch

either in excitement, or slowly and uncertainly, perhaps to have another

attack in a few minutes. These cases, in the few instances in which they

could be followed, were due to faulty feeding and enteritis and showed

either nothing or a mild congestion of the brain. The other variety of

fit is epileptiform, a rapidly developing clonic spasm of all parts of

the body with a tendency to opisthotonos. In one case of this character,

a parrot, no lesions were found in the brain, an enteritis existing

however. Another case concerned a pet Indian Shama I had at my home. He

had been doing well and singing loudly, until one evening he was allowed

to remain in a tobacco-smoke-filled room whereupon next morning he

stopped eating and singing. Later that day the clonic form of

convulsions appeared, growing worse for thirty-six hours or until death.

At autopsy no food was found in the alimentary tract. The brain and cord

were congested grossly, while minutely, perivascular hemorrhages and

marked vacuolization and diffuseness of staining were found in ganglion

cells of the bulb, pons, anterior spinal horns and in the pyramidal

cells of the cerebellum. Happening so promptly after exposure to tobacco

smoke, when the bird was doing well, I venture to associate the two.

ATAXIA.

Incoördination and ataxia are so often observed and under so many

conditions that it is well nigh impossible in any individual case to

give an adequate explanation before death. They are in all probability

the expression of sickness and nothing more in the vast majority of

instances. When they are observed in such cases as the tyromata of the

cerebrum or in certain of the ungulates, they may mean something

definite. In this latter order and to a less extent in carnivores, one

frequently sees weakness and uncertainty of gait in the hind quarters,

the legs being usually coördinate but tending to give way under the

weight of the body.

From a study of veterinary literature and our own material it would seem

that this may have many explanations. In the first place, it may simply

indicate weakness expressing itself in the heaviest part of the body,

the animal inclining its femora forward to assist in supporting the

heavy abdomen. It may be an expression of abdominal pain, the recti

becoming rigid and the quadriceps of the thigh participating in the

protection of the belly. Almost any of the intra-abdominal conditions,

gastroenteritis, mesenteric thrombosis, peritonitis, or diseases of the

psoas muscle and lumbar vertebra, might occasion this attempt at

support. Disease of gluteal muscles, as hemoglobinuric fever, may

produce a palsy of the whole pelvic girdle with weakness of the hind

legs. There may be associated with the weakness of the hind legs a

humped-up condition of the lumbar spine and retraction of the abdomen,

sometimes called “tucked in;” in two definite cases of this last sort we

have found renal pelvic stones and once intestinal sand. Some instances

are undoubtedly due to meningomyelitis or to poliomyelitis and at the

place for this subject a few cases will be discussed. Meningitis has not

been found in the ungulates showing this weakness. There have been

however cases of ataxia in the hind legs of deer and antelopes, which

did not have a ready explanation fitting in with the foregoing. Two of

these we thought might be due to certain grasses in the enclosures and

have changed the exhibition spaces. No conclusion can be drawn from this

as yet. No enterocolic disease could be found nor any lesion of the

sciatic nerve and lumbar enlargement of the cord. We have however

discovered sciatic neuritis in a case like hemoglobinuric fever in a

Burchell’s zebra. The history of the animal is similar to that of this

disease in domestic animals in so far as symptomatology is concerned; in

so far as confinement in a stall is concerned no data is at hand but

death occurred on December 26th in the zebra house whereas he had been

accustomed to go out into the yard all summer and autumn.

MENINGITIS.

The coverings of the brain and cord have not been the seat of the well

known acute inflammations seen in domestic horses and cattle. Eleven

instances of disease in the meninges are recorded but, with very few

exceptions, have been accompanied by other lesions offering a ready

etiological explanation. These cases are however not very instructive

except perhaps three in monkeys where the meningitis seemed to be

secondary to gastroenterocolitis. In one case a colon bacillus was

apparently responsible, in a second no bacteriology was undertaken and a

third was too rotten for the results to be dependable. A focus of

infection aside from the intestinal area could not be found. The only

noteworthy finding was the scantiness of the cerebrospinal fluid and the

almost exclusive subpial exudate; these facts would seem to strengthen

the thought that the virus came through the blood stream. Another case

was due to extension, through the temporal bone to the lateral sinus, of

a necrotizing process beginning in the buccal muscles or parotid gland;

the necrosis bacillus and a host of Gram-positive cocci were found. A

Canadian porcupine suffered with a mucopurulent nasopharyngitis which

involved the deep sinuses, the middle ear and the temporal bone; smears

from the pus over the corresponding cerebral hemisphere and from the

nasal pus showed pneumococcus forms; the lungs were not affected. The

llama which showed the intracapsular fracture of the femur (page 344)

had also hemorrhage into a fibrinous exudate in the mastoid cells with

deep opaque congestion and edema of the pia above the petrous portion of

the temporal bone. Decomposition precluded satisfactory bacteriology but

it is suggested that probably injury in falling started a hemorrhage in

the ear upon which a secondary infection was implanted. What seems a

true meningitis secondary to otitis media and mastoid suppuration was

seen in a marmoset.

A case of the well known but obscure condition known as chronic

productive pachymeningitis was observed in a badger. Although it cannot

be explained it is cited as a matter of record and interest.

American Badger (_Taxidea taxus_). Pachymeningitis externa. The dura

is fast to the skull and cannot be removed. Scattered irregularly over

the entire inner surface of the skull are pale pinhead sized hard

nodules. It is impossible to tell if they are in the dura or the bone.

The brain shows engorged vessels but is otherwise negative.

Two instances of hemorrhagic pachymeningitis associated with cretinism

were seen in wolf cubs. The following notes illustrate both cases.

American Gray Wolf (_Canis mexicanus_). Cretinism. Hemorrhagic

external pachymeningitis with craniotabes. Upon removing the calvarium

a marked craniotabes of the under surface is found and with it a deep

red and purple staining of outside of dura and inner table of skull.

These changes are most marked along the longitudinal sinus at internal

occipital protuberance and along left parietal region. Dura on left

side is distinctly congested. This is also true of pia. The brain and

its base seem normal.

Cyst of the brain. A sooty mangabey (_Cercocebus fuliginosus_) had been

in the Garden for about four months and was apparently an adult normal

animal. It died rather suddenly after a distinct convulsion with

semiconsciousness. At autopsy in addition to a nephritis, a large cyst

was found to occupy the posterior third of the left hemisphere. Its

walls were composed of a thin (one-sixteenth inch) rim of cerebral

substance and the meninges; its contents were clear. The notes do not

record any examination for parasites. This monkey showed no localizing

signs.

TUBERCULOSIS.

Gross tuberculous lesions have been found in the brain in several

specimens with generalized disease but only two cases are of special

interest. A Rhesus macaque (_Macacus rhesus_) suffering with generalized

but chiefly lymphatic tuberculosis, showed a large plaque on the

external surface of the dura over the vertex where it was adherent to a

yellow, fairly firm nodule about ten mm. across. This nodule was deeply

imbedded in the brain substance, barely projecting above the surface,

generally spherical and not encapsulated. There was no peripheral

reactive zone. The meninges were not altered anywhere except as above.

The blood vessels were not especially congested. The pia arachnoid

contained no excess of fluid but the summits of the convolutions were

flattened. The mass was located in the posterior frontal convolution,

near the longitudinal fissure, occupying nearly its whole breadth and

penetrating about one centimetre. It did not enter the fornicate gyrus.

There was a completely degenerated core about two mm. across. The

adjacent bone was beginning to erode. No localizing signs were reported.

The other case, that of a young Drill baboon (_Papio leucophæus_), was

studied with Dr. J. H. W. Rhein and can be reported in the following

condensed notes.

The baboon appeared to be perfectly well until October 18, 1906, when

some lameness in the anterior and posterior extremities on the right

side was observed. This gradually increased, and was associated with

general convulsions. On November 30th, I made an examination and found

the following condition: The right upper and lower extremities were

weaker than on the left side. On the left side the power seemed to be

fair. He was able to hold on to an iron bar with the fingers of the

upper and lower extremities on the right side but in withdrawing the

bar it was not difficult to overcome his grasp and the power on this

side was distinctly less than on the left. The movements of the right

arm were somewhat ataxic, as observed when he made efforts to grasp

the bar. The knee jerks were increased on both sides and appeared to

be equally so. There was no evidence of facial palsy. He moved both

sides of the face equally well at times when he expressed anger or

fear in the facial expression. The tongue seemed to be retracted

equally well on both sides. Tests for hemianopsia were, of course,

unsatisfactory, but he seemed to recognize readily the approach of the

iron bar from both sides. There was no disturbance of the rectal or

bladder functions, although at autopsy the bladder was full. Death

occurred on December 2, 1906. At the autopsy the brain and spinal

cord, with the other organs were examined. The dura was adherent to

the left side of the brain, in the prefrontal region, in the upper

third and when the brain was removed it was observed that an area of

softening lay beneath this point. A small caseous mass was also

observed at the base of the right lung, and beneath the diaphragm on

the right side was a large abscess, partly involving the liver. The

tubercle bacillus was found in the pus removed from the area of

softening beneath the left cortex. A study of the brain revealed the

presence of three foci of softening. The largest one was situated in

the left hemisphere in the prefrontal region, and extended from just

beneath the cortex in the upper third of the region, downward almost

to the base of the brain. This area was cylindrical in shape and

measured 2.5 cm. in its greatest diameter. The area of softening

consisted of caseated material and pus, in which the tubercle bacillus

was found present. The second area of softening was found on the right

side of the brain, much smaller in extent and measuring 1.5 cm.

diameter. There was no pus present in this area, but it consisted of a

circumscribed mass of caseous material. The apex of this area of

softening was just beneath the cortex in the prefrontal region on the

right side, and in the removal of the brain the cortex was torn just

above this area of caseation. This point was .5 cm. in front of the

central fissure and about 1 cm. below the superior surface of the

brain. A third area of softening was observed posteriorly, in the

white substance, in the parieto-occipital region, and measured about 6

mm. in diameter. A study of the sections of the brain shows

beautifully the extent of the destruction of the brain tissue. The

optic thalamus and the lenticular nucleus, and the posterior limb of

the internal capsule, on the left side, are destroyed in part. The

anterior limb of the internal capsule in one section, is preserved,

notwithstanding the fact that the optic thalamus on the same side has

been in large part destroyed. In spite of the fact that the posterior

limb of the internal capsule has been destroyed at some levels, it is

interesting to note that the degeneration of the pyramidal tracts of

the pons and medulla on the opposite side and the lateral columns of

the spinal cord are not intensely—although distinctly—degenerated. It

is very interesting to note that in view of the severe damage to the

posterior limb of the internal capsule on the left side, there was not

more paralysis, for it will be remembered that there was considerable

power of prehension in the right upper and lower extremities.

ENCEPHALOMYELITIS, POLIOMYELITIS.

While, as has been stated, no well defined cases of the recognized

meningocephalic infectious diseases have been observed in the Garden,

there have been several animals in whose cord and brain changes were

found comparable to the infections disease known in man as

poliomyelitis. On several occasions since this disease was recognized as

occurring in epidemic form it has been observed that domestic mammals

and fowls suffered from a similar condition. The general vicinity of

Philadelphia had a low grade epidemic among children during the years

from 1907 to 1912 and it is during this time that most of the cases of a

comparable character were observed among our animals. It is to be

emphasized that attacks were entirely sporadic and the cases did not

appear to bear a relation to one another. This character is quite in

accord with certain of the outbreaks in man. However we cannot state

that the disease is exactly the same as seen in the human being for, as

will be noted in the cited examples, all the pathological features were

not fulfilled.

It is not always possible to differentiate between myelitic disease and

polyneuritis of man or animals. Studied symptomatically the cases in our

records which proved to have degenerative and infiltrative lesions

comparable to poliomyelitis showed gradual but progressive paralysis

expressed by inability to move rather than disinclination—in other words

loss of power rather than restriction because of pain. None of the

animals in which poliomyelitis was demonstrated have exhibited the

ataxia of the hind legs discussed on a previous page nor have we found

myelitic lesions in the few cords from animals suffering with this

weakness. The nearest approach to a cerebrospinal explanation for

weakness and palsy was in a zebra which died with constipation, acute

nephritis, and hepatic perilobular fibrosis. In this animal a pronounced

subpial mononuclear infiltrate was observed, in places involving the

superficial parts of the cerebral gray matter, especially about the

congested vessels of this area. This condition was present to a slight

degree in the cord. There was then a low grade meningoencephalitis but

no nerve cell changes. So far as is known to me no animal showing a

definite local paresis or paraplegia recovered from the attack; had this

occurred we might have observed residual palsies.

In so far as lesions are concerned they are perhaps best illustrated by

the appended cases, but since even in them there is a lack of

uniformity, it may be well to discuss the basic changes of all. The

outstanding abnormality in the microscopic anatomy is the richness of

small mononuclear cells beneath the pia, both spinal and cerebral,

around the smaller blood vessels and to a lesser extent around the

multipolar cells of the gray matter. These do not present the dense

colonization often seen in the acute cases of infantile paralysis in man

but are prominent in comparison to normal nervous tissue. Hemorrhages or

at least small groups of erythrocytes outside of blood vessels are seen

here and there. Vacuolization of ganglion cells is variable, being

prominent in some, trifling or absent in others. Glial proliferation is

often quite marked, and in one case to be cited seems the prominent

lesion.

The animals in which meningopoliomyelitis has been found were three

monkeys, two Canadian lynx, a bear and a raccoon; about a score of cords

from other animals with some kind of palsy have been studied

microscopically without discovering it. The following cases illustrate

our material. The only instance of two cases in close relation concerns

the lynx (_Felis canadensis_). They occupied the same cage and died

twelve days apart. No symptoms were recorded until a few days before

death when a general paralysis appeared, deepening to completeness on

the day of death. No case occurred in neighboring cages. Doctor Rhein

studied all these cases, and his notes are used for these records.

Portions of the lumbar and cervical enlargements and of the thoracic

regions of the cord were stained with hemalum and acid fuchsin and with

thionin. The pia was slightly infiltrated. There was some cellular

infiltration of the anterior septum, and the vessels here showed an

increase in the nuclei of the walls and a slight perivascular

infiltration. The pial infiltration seemed to be equally distributed in

the entire circumference of the cord, although perhaps a little more

marked over the anterior and posterior septa. The vessels of the gray

matter were congested and the walls of the vessels in most part showed a

proliferation of the nuclei. There were a few small hemorrhages into the

gray matter, probably agonal. As compared with the human cord and the

cords of monkeys, antelopes and dogs, there was an unusually large

number of glia nuclei, which, if found in the human cord, would be

looked upon as a proliferation process. In some cases these nuclei were

heaped together in masses, and were evidently pathological. There was

also, about the ganglion cells, some pericellular round cell

infiltration, and this was more marked around a few cells which were

almost entirely destroyed. The ganglion cells themselves were swollen.

Some showed eccentric nuclei, and many of them stained poorly, while one

or two showed distinct vacuolization. In one field a ganglion cell was

partly destroyed by a recent hemorrhage. There were, however, a number

of cells which appeared normal. This process seemed to be fairly

distinct in the lumbar and cervical enlargements, but was not clearly

demonstrated in the sections from the dorsal region. The cellular

infiltration of the horns was evidently not leucocytic, but presented

the appearance of a connective tissue proliferation. Although these are

not the exact lesions found in poliomyelitis in the human animal, they

are at least suggestive of the same process since the infiltrating cells

are of the lymphatic or connective tissue types. There is no acute

inflammatory leucocytic infiltrate.

A weeper cebus (_Cebus capucinus_) ever since he was received acted in

such a peculiar manner, seeming to have only partial control of his

movements, that he was known as the “Crazy Monkey.” There was no history

of illness before death. Pathological diagnosis: Chronic enterocolitis,

chronic adhesive pericarditis, early interstitial change in kidney,

edema of lungs, meningitis and poliomyelitis. The pia of the paracentral

cortex was thickened and was the seat of a round cell infiltration of

moderate degree, the cells being of the mononuclear type. The blood

vessels of the cortex were congested and the nuclei of the walls were

increased. The round cell infiltration of the pia had in some places

extended into the cortical layers. The pia surrounding the medulla

oblongata was also the seat of a slight round cell infiltration. The pia

of the spinal cord, however, did not show any cellular infiltration. The

cells of the anterior horns of the spinal gray matter were extensively

diseased, being swollen in places, some surrounded by a glia

proliferation and many with marked vacuolization.

A common raccoon (_Procyon lotor_) was observed in the laboratory to

have complete paralysis of the anterior and partial paralysis of the

posterior extremities. This latter was almost complete in muscles

controlling the feet, while the thigh and hip muscles showed some

irregular incoördinate movements. Respiration shallow but regular.

History shows that the power of the extremities began to fail about a

month before death and was absolutely lost in the fore extremities three

days before the animal was killed. Diagnosis: Poliomyelitis. Examination

of the central nervous system showed the presence of marked round cell

infiltration of pia of cortex and of spinal cord, more particularly in

the lower thoracic and lumbar regions. Ganglion cells in the lumbar

region were markedly diseased. There were numerous old and fresh

hemorrhages and a moderate degree of round cell infiltration in the

anterior horns. Two young of this animal, born three months before its

death, showed weakness and gradual increasing paralysis of their

extremities beginning when three months old (that is at the time of the

death of their mother), and lasting until their death, one in the

seventh and one in the eighth month of life. These were found not to

have changes in the central nervous system, but there was sufficient

rachitis to account for this paralysis.

The only tumor of the central nervous system found among these animals

occurred in an Undulated Grass Parrakeet (_Melopsittacus undulatus_).

The gross notes are very vague but the microscopy is suggestive of a

glioma. The growth in the brain consists of large irregular masses of

large cells with vesicular nuclei and pale homogeneous protoplasm.

“Scattered between these accumulations are irregular strands of spindle

cells, with spindle-shaped nuclei, taking the hematoxylin very deeply.

The supporting tissue is almost without cells, taking the eosin faintly,

and is quite loosely arranged. No fibrils are seen among the cells. The

blood vessels are congested, and at one place there is a small

hemorrhage. The vessel walls are the same as the rest of the connective

tissue. There is a slightly atypical metastasis in the liver.”

A case, the identity of which is still undecided, was observed in a

Green Monkey (_Cercopithecus callitrichus_); it may belong among the

gliomata or glioses. There was in the middle of this monkey’s cerebrum a

gray area about 3 × 2 × 1 cm. with a softened centre, the more solid

parts being found under the microscope to consist of glia tissue, blood

vessels and degenerated cells. No true gliomatous formations could be

discovered. Because of the indefiniteness of the lesion, it is not

included in the tumors or inflammations. Clinically the effect of the

change was to cause blindness and ataxia but motor power was not greatly

impaired.

A very small number of tumors of the brain in wild animals is on record

in the English and German literature, perhaps the most interesting being

what resembles in description a subdural neurocytoma reported by Wilson

in the _Proceedings of the London Zoological Society_, 1908. The mass

was separate from the cerebellum, but had hollowed out a place for

itself in this part of the hind-brain.

BRAIN WEIGHTS.

The policy of preserving the brain of all species enables us to record

in the accompanying list the weights of a large number of specimens. In

order that the figures may have a representative and comparative value

only those are given where the total body weight of the animal is also

known. The specimens were removed by the laboratory staff, most of them

by one person, and by the same technique. All brains were weighed

immediately upon removal from the body, no preservative being near the

organ. The brains were themselves externally normal. Our technician is

skillful in removing the organ, practically always getting the pituitary

body, and cutting off the brain stem at the foramen magnum, the pia

remaining but the dura removed. Because the specimens were taken, in

practically all cases, from animals that died in the Park, and because

of the shortness of the list (196), it seems wise not to attempt

conclusions referable to comparative weights of the different orders and

families. However, the data seem worthy of record because it is doubtful

if anywhere one can find so many weights taken under comparable

conditions by the same personnel. One can find a considerable list of

brain weights and values in many publications throughout the literature,

notably in an article by Ziehen in Bardeleben’s _Handbuch der Anatomie_

(Vol. IV, Abt. III 363), but from no single source are there so many

varieties or so long a list. Ziehen’s tables are compiled from the

literature and therefore represent data collected under different

conditions, many of which were probably pathological. The appended

figures are to be considered as raw material collected under uniform

conditions.

Examination of the figures bears out in a measure some of the remarks

made by Ziehen, notably those which indicate that between large and

small varieties of the same general group, the smaller has the greater

brain weight value and that the youthful animal has more brain than the

adult.

The brains at the museum are fixed in saline-formaldehyde—sufficient

strength of the former to suspend the organ in the container and four

percentage of the latter. When fixation is complete, as indicated by

density, preservation is done in one per cent. formaldehyde, the organ,

usually bound in gauze, being laid in cotton. A list of important

references is added to the weight tables—some antedating Ziehen’s

articles, but principally those that have appeared since the publication

of his monograph.

PRINCIPAL REFERENCES TO THE RELATIVE WEIGHT OF THE BRAIN

ZIEHEN: In _Bardeleben’s Handbuch der Anatomie des Menschen_, Vol. 4,

pt. 3.

ZIEHEN: _Handbuch der Anatomie des Nervensystems_, Jena, 1903.

GIRARD: _Bulletin de l’Institut Gen. Psychologie_, Vol. 7, p. 53.

VON BUSCHAU: _Real Encyclopedie der Gesamten Heilkunde 3. Aufl._

VON BUSCHAU: _Neurologisches Zentralbl._, 1897, March.

BRANDT: _Bull. de la Soc. Imperial des Naturalistes de Moscow_, 1867,

40, pt. 2, 525.

MIES: _Verhandl. der Gesellsch. deutscher Naturforsch und Arzte_, 1898,

353.

DHERE ET LAPICQUE: _Archives de la Physiologie_, October, 1898.

LAPICQUE ET GIRARD: _C. R. des Sceances de l’Academie de Science_,

Paris, 1905, 140, 1057.

LAPICQUE: _Bulletin de Museum d’Histoire Naturelle_, 1909, No. 7, 408.

LAPICQUE: _Revue du Mois_, Paris, April, 1908, 445.

LAPICQUE: _Bulletin et Memoires de la Société d’Anthropologie de Paris_,

1907, 5, Vol. 8, No. 3, 261.

LAPICQUE: _Biologica_, Vol. 2, 1912, p. 257.

FUNK: _Inaug. Dissert. Wurzburg_, 1911.

POYNTER: _Cerebral Anthropology_, Lincoln, 1913.

MOLLISON: _Arch. für Anthropologie_, 1914, XIII, 388.

HULTGREN: _Das Hirngewicht des Menschen_, Upsala, 1912.

WEBER: _Festschrift für Karl Gegenbauer_, 1898.

DUBOIS: _Bulletin de la Soc. Anthropologie_, Paris, 1897, 337.

DUBOIS: _Archiv. für Anthropologie_, Vol. 25, 1898.

DUBOIS: _Proc. Sci. K. Acad. Wet., Amsterdam_, 1914, 16, 647.

DUBOIS: _Zeitschrift für Morph. und Anthropologie_, 1914, Vol. 18, 323.

MARCHAND: _Hirngewicht des Menschen_, Leipsig, 1902.

RUDOLPH: _Beiträge zur Path. Anatomie_, Jena, 58, 1914, 48.

KRAEMER: _Mitt. der Deutsch. Landwehrgesell_, 29, 1914, 55.

TABLE 18.—_Giving the Actual Weight of the Brain and the Relation of this to that

of the Body in 196 Animals._

════════════════════╤═══╤══════╤═══════════╤══════╤═════════╤════════╤══════╤══════

Order Family │Sex│Known │Development│ Time │Condition│ Body │Brain │Grams

│ │Age at│ │ in │ │ Weight │Weight│Brain

│ │Death │ │Garden│ │in Grams│ in │ Per

│ │ │ │ │ │ │Grams │ Kilo

│ │ │ │ │ │ │ │ of

│ │ │ │ │ │ │ │ Body

│ │ │ │ │ │ │ │Weight

Genus Species │ „ │ „ │ „ │ „ │ „ │ „ │ „ │ „

Common Name │ „ │ „ │ „ │ „ │ „ │ „ │ „ │ „

────────────────────┼───┼──────┼───────────┼──────┼─────────┼────────┼──────┼──────

PRIMATESA: │ │ │ │ │ │ │ │

SIMIADÆ: │ │ │ │ │ │ │ │

Simia satyrus, │ │ │ │ │ │ │ │

Orang utan │ ♂ │ │Immature │4 yrs.│Good │ 15,500.│ 405.│ 26.1

│ │ │ │6 mo. │ │ │ │

Orang utan │ ♀ │ │Immature │4 yrs.│Thin │ 22,178.│ 300.│ 13.4

│ │ │ │2 mo. │ │ │ │

Hylobates │ │ │ │ │ │ │ │

hainanus, │ │ │ │ │ │ │ │

Hainan Gibbon │ ♂ │ │Mature │4 yrs.│Good │ 5,900.│ 115.│ 19.4

│ │ │ │3 mo. │ │ │ │

Hylobates │ │ │ │ │ │ │ │

leuciscus, │ │ │ │ │ │ │ │

Silver Gibbon │ ♀ │ │Mature │14 │Very thin│ 3,030.│ 75.│ 24.7

│ │ │ │days │ │ │ │

│ │ │ │ │ │ │ │

CERCOPITHECIDÆ: │ │ │ │ │ │ │ │

Presbytis │ │ │ │ │ │ │ │

cephalopterus, │ │ │ │ │ │ │ │

Ceylon Entellus │ ♂ │ │Mature │1 mo. │Good │ 4,080.│ 58.│ 14.2

Cercopithecus │ │ │ │ │ │ │ │

sabæus, │ │ │ │ │ │ │ │

Grivet Monkey │ ♀ │ │Mature │14 │Good │ 3,530.│ 65.│ 18.4

│ │ │ │yrs. │ │ │ │

Cercopithecus │ │ │ │ │ │ │ │

patas, │ │ │ │ │ │ │ │

Red Monkey │ ♂ │ │Mature │2 yrs.│Good │ 5,060.│ 105.│ 20.7

│ │ │ │9 mo. │ │ │ │

Cercocebus │ │ │ │ │ │ │ │

fuliginosus, │ │ │ │ │ │ │ │

Sooty Mangabey │ ♀ │ │ │3 mo. │Good │ 3,342.│ 105.│ 31.4

Macacus arctoides,│ │ │ │ │ │ │ │

Brown Macaque │ ♂ │ │ │3 yrs.│Good │ 3,161.│ 100.│ 31.7

│ │ │ │6 mo. │ │ │ │

Macacus │ │ │ │ │ │ │ │

nemestrinus, │ │ │ │ │ │ │ │

Pigtailed │ ♀ │ │ │4 yrs │Very Thin│ 4,560.│ 100.│ 21.9

Macaque │ │ │ │3 mo. │ │ │ │

Pigtailed │ ♀ │10 mo.│Baby │10 mo.│Good │ 1,390.│ 67.│ 48.2

Macaque │ │ │ │ │ │ │ │

Macacus rhesus, │ │ │ │ │ │ │ │

Rhesus Macaque │ ♂ │6 mo. │Baby │6 mo. │Good │ 462.│ 67.│ 145.

Papio porcarius, │ │ │ │ │ │ │ │

Chacma Baboon │ ♂ │ │Mature │1 wk. │Thin │ 12,300.│ 180.│ 14.6

Papio │ │ │ │ │ │ │ │

cynocephalus, │ │ │ │ │ │ │ │

Yellow Baboon │ ♂ │ │Mature │4 yrs.│ │ 8,942.│ 140.│ 15.6

│ │ │ │6 mo. │ │ │ │

│ │ │ │ │ │ │ │

CEBIDÆ: │ │ │ │ │ │ │ │

Ateles ater, │ │ │ │ │ │ │ │

Black Spider │ ♀ │ │ │1 mo. │Good │ 1,790.│ 125.│ 70.

Monkey │ │ │ │ │ │ │ │

Black Spider │ ♀ │ │ │2 mo. │Good │ 2,475.│ 105.│ 42.5

Monkey │ │ │ │ │ │ │ │

Black Spider │ ♂ │ │ │2 mo. │Good │ 3,630.│ 125.│ 34.4

Monkey │ │ │ │ │ │ │ │

Lagothrix │ │ │ │ │ │ │ │

lagotricha, │ │ │ │ │ │ │ │

Woolly Monkey │ ♀ │ │ │9 mo. │Thin │ 1,634.│ 82.│ 50.3

Cebus fatuellus, │ │ │ │ │ │ │ │

Brown Cebus │ ♀ │ │ │2 yrs.│Thin │ 1,500.│ 60.│ 40.

Cebus albifrons, │ │ │ │ │ │ │ │

White fronted │ ♂ │ │ │ │ │ 1,750.│ 61.│ 34.8

Cebus │ │ │ │ │ │ │ │

Aotes vociferans, │ │ │ │ │ │ │ │

Noisy │ ♂ │ │ │2 wks.│Good │ 480.│ 20.│ 41.7

Douroucouli │ │ │ │ │ │ │ │

│ │ │ │ │ │ │ │

CALLITRICHIDÆ: │ │ │ │ │ │ │ │

Callithrix │ │ │ │ │ │ │ │

pencillata, │ │ │ │ │ │ │ │

Black eared │ ♂ │ │ │1 yr. │Good │ 135.│ 10.│ 73.

Marmoset │ │ │ │ │ │ │ │

Black eared │ ♂ │ │ │6 mo. │Good │ 250.│ 15.│ 60.

Marmoset │ │ │ │ │ │ │ │

Leontocebus │ │ │ │ │ │ │ │

œdipus, │ │ │ │ │ │ │ │

Pinche Marmoset │ ♂ │ │ │1 wk. │Good │ 167.│ 14.│ 84.

│ │ │ │ │ │ │ │

LEMURES: │ │ │ │ │ │ │ │

LEMURIDÆ: │ │ │ │ │ │ │ │

Lemur catta, │ │ │ │ │ │ │ │

Ring tailed │ ♀ │Mature│ │7 yrs.│Good │ 1,470.│ 30.│ 20.4

Lemur │ │ │ │ │ │ │ │

Ring tailed │ ♀ │ │ │1 yr. │Good │ 1,240.│ 20.│ 16.

Lemur │ │ │ │3 mo. │ │ │ │

Lemur mongoz, │ │ │ │ │ │ │ │

Mongoose Lemur │ ♀ │ │ │2 yrs.│Good │ 1,457.│ 20.│ 13.8

Galago maholi, │ │ │ │ │ │ │ │

Maholi Galago │ ♂ │5 yrs.│Mature │5 yrs.│Good │ 100.│ 4.│ 40.

│ │3 mo. │ │3 mo. │ │ │ │

│ │ │ │ │ │ │ │

CARNIVORA: │ │ │ │ │ │ │ │

FELIDÆ: │ │ │ │ │ │ │ │

Felis viverrina, │ │ │ │ │ │ │ │

Fishing Cat │ ♂ │ │ │10 mo.│Good │ 7,000.│ 60.│ 8.5

Felis chaus, │ │ │ │ │ │ │ │

Jungle Cat │ ♀ │ │Mature │5 yrs.│Good │ 3,640.│ 45.│ 12.2

│ │ │ │3 mo. │ │ │ │

Felis ruffus, │ │ │ │ │ │ │ │

American Wild │ ♀ │ │ │4 yrs.│Thin │ 4,402.│ 50.│ 11.1

Cat │ │ │ │ │ │ │ │

Felis onca, │ │ │ │ │ │ │ │

Jaguar │ ♀ │20 │Mature │15 │Very thin│ 29,500.│ 170.│ 5.7

│ │yrs. │ │yrs. │ │ │ │

Felis eyra, │ │ │ │ │ │ │ │

Eyra │ ♂ │ │ │3 mo. │Good │ 5,000.│ 44.│ 8.8

Felis canadensis, │ │ │ │ │ │ │ │

Canada Lynx │ ♀ │ │Mature │4 yrs.│Very thin│ 7,270.│ 80.│ 11.

│ │ │ │6 mo. │ │ │ │

Felis │ │ │ │ │ │ │ │

chibigonazon, │ │ │ │ │ │ │ │

Brazilian Ocelot│ ♀ │ │Young │1 mo. │Thin │ 1,350.│ 35.│ 26.

Felis pardalis, │ │ │ │ │ │ │ │

Common Ocelot │ ♀ │ │ │10 mo.│Good │ 5,800.│ 50.│ 8.6

Common Ocelot │ ♂ │ │Young │2 mo. │Thin │ 2,700.│ 45.│ 16.6

Felis concolor, │ │ │ │ │ │ │ │

Puma │ ♂ │ │ │ │Good │ 52,700.│ 150.│ 2.8

Puma │ ♀ │ │Mature │8 yrs.│Very thin│ 29,500.│ 50.│ 1.69

│ │ │ │6 mo. │ │ │ │

Puma │ ♂ │ │Baby │ │Good │ 1,067.│ 55.│ 51.5

Puma │ ♀ │ │Baby │ │Good │ 998.│ 55.│ 55.

Felis tigris, │ │ │ │ │ │ │ │

Bengal Tiger │ ♀ │ │Mature │12 │Fair │ 66,000.│ 250.│ 3.8

│ │ │ │yrs. │ │ │ │

Bengal Tiger │ ♂ │ │Mature │12 │Very thin│ 91,000.│ 240.│ 2.6

│ │ │ │yrs. │ │ │ │

Felis uncia, │ │ │ │ │ │ │ │

Snow Leopard │ ♀ │ │Mature │8 yrs.│Good │ 22,700.│ 120.│ 5.3

│ │ │ │ │ │ │ │

HYÆNIDÆ: │ │ │ │ │ │ │ │

Hyæna hyæna, │ │ │ │ │ │ │ │

Striped Hyæna │ ♂ │ │Mature │4 yrs.│Poor │ 27,200.│ 92.│ 3.3

│ │ │ │ 3 mo.│ │ │ │

Striped Hyæna │ ♂ │ │Mature │8 yrs.│Good │ 36,300.│ 90.│ 2.4

│ │ │ │10 mo.│ │ │ │

│ │ │ │ │ │ │ │

CANIDÆ: │ │ │ │ │ │ │ │

Canis │ │ │ │ │ │ │ │

procyonoides, │ │ │ │ │ │ │ │

Raccoon-like Dog│ ♀ │ │Mature │3 yrs.│Good │ 4,770.│ 25.│ 5.2

Raccoon-like Dog│ ♀ │ │ │ │Good │ 4,900.│ 35.│ 7.1

Canis familiaris, │ │ │ │ │ │ │ │

Eskimo Dog │ ♂ │ │Mature │ │Very thin│ 36,300.│ 100.│ 2.7

Canis cinereo │ │ │ │ │ │ │ │

argenteus, │ │ │ │ │ │ │ │

Gray Fox │ ♀ │ │Mature │3 yrs.│Good │ 2,652.│ 40.│ 15.

Canis cinereus │ │ │ │ │ │ │ │

argenteus scotti, │ │ │ │ │ │ │ │

Scott’s Gray Fox│ ♀ │ │Mature │2 yrs.│Good │ 2,200.│ 53.│ 25.

│ │ │ │6 mo. │ │ │ │

Canis chama, │ │ │ │ │ │ │ │

Silver Fox │ ♂ │ │ │7 mo. │Good │ 3,325.│ 40.│ 12.

Canis mesomelas, │ │ │ │ │ │ │ │

Blackbacked │ ♂ │ │ │2 yrs.│Good │ 6,000.│ 60.│ 10.

Jackal. │ │ │ │6 mo. │ │ │ │

Blackbacked │ ♀ │ │ │ │ │ 3,500.│ 70.│ 20.

Jackal │ │ │ │ │ │ │ │

│ │ │ │ │ │ │ │

MUSTELIDÆ: │ │ │ │ │ │ │ │

Mustela foina, │ │ │ │ │ │ │ │

Beech Marten │ ♀ │ │Mature │3 yrs.│Good │ 810.│ 15.│ 18.3

Mustela americana,│ │ │ │ │ │ │ │

Pine Marten │ ♂ │ │Mature │4 yrs.│Good │ 680.│ 13.│ 19.

Gulo gulo, │ │ │ │ │ │ │ │

Wolverine │ ♀ │ │ │3 yrs.│Good │ 5,700.│ 75.│ 13.1

│ │ │ │3 mo. │ │ │ │

Galictis barbara, │ │ │ │ │ │ │ │

Tayra. │ ♂ │ │ │7 mo. │Good │ 1,480.│ 55.│ 37.

Mephitis │ │ │ │ │ │ │ │

mephitica, │ │ │ │ │ │ │ │

Common Skunk │ ♀ │ │ │6 mo. │Good │ 1,755.│ 6.│ 3.4

Common Skunk │ ♀ │ │ │2 wks.│Good │ 1,700.│ 7.│ 4.1

Meles meles, │ │ │ │ │ │ │ │

European Badger │ ♂ │ │ │3 yrs.│Good │ 7,473.│ 46.│ 6.

│ │ │ │ │ │ │ │

PROCYONIDÆ: │ │ │ │ │ │ │ │

Procyon lotor, │ │ │ │ │ │ │ │

Common Raccoon │ ♂ │ │Mature │7 yrs.│Good │ 9,000.│ 42.│ 4.6

│ │ │ │3 mo. │ │ │ │

Common Raccoon │ ♀ │ │Mature │9 yrs.│Good │ 5,450.│ 37.│ 6.9

│ │ │ │2 mo. │ │ │ │

Procyon lotor │ │ │ │ │ │ │ │

hernandezi, │ │ │ │ │ │ │ │

Mexican Raccoon │ ♀ │ │ │2 yrs.│Good │ 6,130.│ 40.│ 6.5

Nasua nasua, │ │ │ │ │ │ │ │

Ring tailed │ ♂ │ │ │1 yr. │Good │ 1,600.│ 40.│ 25.

Coati │ │ │ │4 mo. │ │ │ │

Ring tailed │ ♂ │ │ │10 mo.│Good │ 1,600.│ 35.│ 24.3

Coati │ │ │ │ │ │ │ │

Nasua narica, │ │ │ │ │ │ │ │

White nosed │ ♂ │Mature│ │8 yrs.│Very thin│ 5,000.│ 44.│ 8.8

Coati │ │ │ │ │ │ │ │

Potos │ │ │ │ │ │ │ │

caudivolvulus, │ │ │ │ │ │ │ │

Kinkajou │ │Mature│ │3 yrs.│Good │ 1,440.│ 35.│ 24.2

│ │ │ │2 mo. │ │ │ │

│ │ │ │ │ │ │ │

URSIDÆ: │ │ │ │ │ │ │ │

Ursus malayanus, │ │ │ │ │ │ │ │

Sun Bear │ │ │ │1 yr. │Good │ 41,000.│ 125.│ 3.5

│ │ │ │9 mo. │ │ │ │

Ursus beringiana, │ │ │ │ │ │ │ │

Kamchatkan Bear │ ♀ │ │ │ │Very thin│ 31,800.│ 315.│ 9.9

│ │ │ │ │ │ │ │

PINNIPEDIA: │ │ │ │ │ │ │ │

OTARIIDÆ: │ │ │ │ │ │ │ │

Eumetopias │ │ │ │ │ │ │ │

stelleri, │ │ │ │ │ │ │ │

Steller’s Sea │ ♂ │ │ │4 yrs.│Very thin│120,400.│ 515.│ 4.27

Lion │ │ │ │ │ │ │ │

Zalophus │ │ │ │ │ │ │ │

californianus, │ │ │ │ │ │ │ │

California Hair │ ♂ │ │Mature │6 yrs.│Very good│ 94,000.│ 420.│ 4.46

Seal │ │ │ │9 mo. │ │ │ │

│ │ │ │ │ │ │ │

RODENTIA: │ │ │ │ │ │ │ │

MURIDÆ: │ │ │ │ │ │ │ │

Peromyscus │ │ │ │ │ │ │ │

leucopus, │ │ │ │ │ │ │ │

White footed Mouse│ ♀ │5 yrs.│Mature │5 yrs.│Good │ 39.│ 1.│ 25.6

│ │ │ │ │ │ │ │

CASTORIDÆ: │ │ │ │ │ │ │ │

Castor canadensis,│ │ │ │ │ │ │ │

American Beaver │ ♀ │ │ │8 yrs.│Good │ 10,000.│ 40.│ 4.

│ │ │ │2 mo. │ │ │ │

│ │ │ │ │ │ │ │

OCTODONTIDÆ: │ │ │ │ │ │ │ │

Myocastor coypus, │ │ │ │ │ │ │ │

Coypu │ ♀ │ │ │ │Good │ 2,000.│ 20.│ 10.

│ │ │ │ │ │ │ │

HYSTRICIDÆ: │ │ │ │ │ │ │ │

Hystrix │ │ │ │ │ │ │ │

longicauda, │ │ │ │ │ │ │ │

Malaccan │ ♀ │ │Mature │18 │Thin │ 6,000.│ 26.│ 4.3

Porcupine │ │ │ │yrs. │ │ │ │

Erethizon dorsatus│ │ │ │ │ │ │ │

dorsatus, │ │ │ │ │ │ │ │

Canada Porcupine│ ♀ │ │ │2 mo. │Good │ 4,065.│ 20.│ 4.9

Coendon │ │ │ │ │ │ │ │

prehensilis, │ │ │ │ │ │ │ │

Brazilian Tree │ ♀ │ │ │1 wk. │Good │ 480.│ 14.│ 29.1

Porcupine │ │ │ │ │ │ │ │

│ │ │ │ │ │ │ │

CAVIIDÆ: │ │ │ │ │ │ │ │

Cavia porcella, │ │ │ │ │ │ │ │

Wild Guinea-Pig │ ♂ │ │Mature │6 yrs.│Good │ 320.│ 4.│ 12.5

│ │ │ │2 mo. │ │ │ │

Hydrochœrus │ │ │ │ │ │ │ │

hydrochœrus, │ │ │ │ │ │ │ │

Capybara │ ♂ │ │ │1 mo. │Good │ 19,000.│ 50.│ 2.63

│ │ │ │ │ │ │ │

PROBOSCIDEA: │ │ │ │ │ │ │ │

Elephas maximus, │ │ │ │ │ │ │ │

Asiatic Elephant│ ♂ │3 yrs.│Young │1 mo. │Good │241,000.│3,432.│ 14.1

│ │ │ │ │ │ │ │

HYRACOIDEA: │ │ │ │ │ │ │ │

HYRACIDÆ: │ │ │ │ │ │ │ │

Procaria capensis,│ │ │ │ │ │ │ │

Cape Hyrax │ ♂ │ │ │8 mo. │Good │ 1,800.│ 15.│ 8.3

Cape Hyrax │ ♀ │ │ │1 yr. │Good │ 2,170.│ 20.│ 9.2

│ │ │ │9 mo. │ │ │ │

│ │ │ │ │ │ │ │

UNGULATA: │ │ │ │ │ │ │ │

TAPIRIDÆ: │ │ │ │ │ │ │ │

Tapirus indicus, │ │ │ │ │ │ │ │

Malayan Tapir │ ♀ │ │Mature │7 yrs.│Thin │250,000.│ 300.│ 1.2

│ │ │ │4 mo. │ │ │ │

Malayan Tapir │ ♂ │ │Young │3 mo. │Good │ 80,000.│ 225.│ 2.8

│ │ │ │ │ │ │ │

EQUIDÆ: │ │ │ │ │ │ │ │

Equus prjivalskii,│ │ │ │ │ │ │ │

Wild Horse │ ♀ │1 wk. │Baby │1 wk. │Good │ 22,700.│ 330.│ 14.

Equus burchelli, │ │ │ │ │ │ │ │

Burchell’s Zebra│ ♂ │ │Mature │6 yrs.│Good │341,000.│ 645.│ 1.9

│ │ │ │ │ │ │ │

BOVIDÆ: │ │ │ │ │ │ │ │

Strepsiceros │ │ │ │ │ │ │ │

capensis, │ │ │ │ │ │ │ │

Greater Kudu │ ♂ │ │ │4 mo. │Thin │285,000.│ 290.│ 2.2

Cobus leche, │ │ │ │ │ │ │ │

Leche Antelope │ ♀ │ │Mature │10 │Good │ 52,700.│ 200.│ 3.8

│ │ │ │yrs. 6│ │ │ │

│ │ │ │mo. │ │ │ │

Damaliscus │ │ │ │ │ │ │ │

albifrons, │ │ │ │ │ │ │ │

Blessbok │ ♂ │ │Mature │11 │Good │ 58,100.│ 245.│ 4.2

│ │ │ │yrs. │ │ │ │

Boselaphus │ │ │ │ │ │ │ │

tragocamelus, │ │ │ │ │ │ │ │

Nylghaie │ ♀ │ │ │2 yrs.│Good │136,300.│ 310.│ 2.3

│ │ │ │2 mo. │ │ │ │

Poephagus │ │ │ │ │ │ │ │

grunniens, │ │ │ │ │ │ │ │

Yak │ ♂ │3 yrs.│Young runt │3 yrs.│Runt │114,000.│ 290.│ 2.5

│ │6 mo. │ │6 mo. │ │ │ │

Yak │ ♀ │ │Mature │5 yrs.│Thin │177,000.│ 385.│ 2.2

Taurotragus oryx │ │ │ │ │ │ │ │

livingstonii, │ │ │ │ │ │ │ │

Livingstone’s │ ♀ │ │Old │13 │Good │327,000.│ 415.│ 1.3

Eland │ │ │ │yrs. │ │ │ │

Hemitragus │ │ │ │ │ │ │ │

jemlaicus, │ │ │ │ │ │ │ │

Himalayan Thar │ ♂ │ │ │2 yrs.│Good │ 31,800.│ 165.│ 5.2

│ │ │ │2 mo. │ │ │ │

Himalayan Thar │ ♂ │9 mo. │Young │9 mo. │Good │ 9,100.│ 130.│ 16.

Ovis tragelaphus, │ │ │ │ │ │ │ │

Aoudad │ ♂ │ │ │3 yrs.│Good │ 77,200.│ 233.│ 3.

│ │ │ │2 mo. │ │ │ │

Aoudad │ ♀ │ │Old │3 yrs.│Good │ 41,000.│ 195.│ 4.8

│ │ │ │6 mo. │ │ │ │

│ │ │ │ │ │ │ │

GIRAFFIDÆ: │ │ │ │ │ │ │ │

Giraffa │ │ │ │ │ │ │ │

camelopardalis, │ │ │ │ │ │ │ │

Giraffe │ ♀ │ │ │5 yrs.│Good │500,000.│ 630.│ 1.2

│ │ │ │8 mo. │ │ │ │

Giraffa capensis, │ │ │ │ │ │ │ │

Giraffe │ ♂ │ │Old │7 mo. │ │383,000.│ 670.│ 1.7

(Southern) │ │ │ │ │ │ │ │

│ │ │ │ │ │ │ │

CERVIDÆ: │ │ │ │ │ │ │ │

Cervus duvanceli, │ │ │ │ │ │ │ │

Barasingha Deer │ ♀ │1 mo. │Baby │1 mo. │Good │ 9,500.│ 121.│ 13.

Cervus eldi, │ │ │ │ │ │ │ │

Eld’s Deer │ ♂ │ │ │ │Good │ 59,000.│ 225.│ 3.8

Cervus elaphus, │ │ │ │ │ │ │ │

Red Deer │ ♀ │ │ │ │Good │ 72,700.│ 310.│ 4.4

Cervus porcinus, │ │ │ │ │ │ │ │

Hog Deer │ ♂ │11 mo.│Young │11 mo.│Good │ 25,000.│ 130.│ 5.2

Hog Deer │ ♂ │ │ │3 yrs.│Good │ 41,000.│ 125.│ 3.

│ │ │ │4 mo. │ │ │ │

Cervus sika │ │ │ │ │ │ │ │

manchuricus, │ │ │ │ │ │ │ │

Manchurian Sika │ ♂ │ │Mature │6 yrs.│Good │ 56,800.│ 265.│ 4.6

Deer │ │ │ │3 mo. │ │ │ │

Cervus │ │ │ │ │ │ │ │

cashmirianus, │ │ │ │ │ │ │ │

Kashmir Deer │ ♂ │ │ │3 yrs.│Fair │ 56,800.│ 275.│ 4.6

│ │ │ │4 mo. │ │ │ │

│ │ │ │ │ │ │ │

CAMELIDÆ: │ │ │ │ │ │ │ │

Camelus │ │ │ │ │ │ │ │

bactrianus, │ │ │ │ │ │ │ │

Bactrian Camel │ ♂ │ │Mature │11 │Fair │430,000.│ 610.│ 1.4

│ │ │ │yrs. │ │ │ │

Camelus │ │ │ │ │ │ │ │

dromidarius, │ │ │ │ │ │ │ │

Common Camel │ ♀ │ │Mature │5 yrs.│Fair │472,700.│ 465.│ .98

│ │ │ │ │ │ │ │

HIPPOPOTAMIDÆ: │ │ │ │ │ │ │ │

Hippopotamus │ │ │ │ │ │ │ │

amphibius, │ │ │ │ │ │ │ │

Hippopotamus │ ♂ │1 mo. │Baby │1 mo. │Good │ 40,000.│ 195.│ 4.87

│ │ │ │ │ │ │ │

SUIDÆ: │ │ │ │ │ │ │ │

Macrocephalus │ │ │ │ │ │ │ │

africanus, │ │ │ │ │ │ │ │

Wart Hog │ ♀ │ │Mature │7 yrs.│Good │ 59,000.│ 151.│ 2.5

│ │ │ │9 mo. │ │ │ │

Wart Hog │ ♂ │ │ │2 yrs.│Good │ 82,700.│ 150.│ 1.8

│ │ │ │9 mo. │ │ │ │

Wart Hog. │ ♂ │ │ │ │Good │ 90,000.│ 158.│ 1.7

│ │ │ │ │ │ │ │

TAYASSUIDÆ: │ │ │ │ │ │ │ │

Tayassu tajacu, │ │ │ │ │ │ │ │

Peccary │ ♀ │ │Mature │6 yrs.│Good │ 19,650.│ 95.│ 4.8

│ │ │ │6 mo. │ │ │ │

Peccary │ ♂ │ │ │3 yrs.│Good │ 22,700.│ 75.│ 3.3

│ │ │ │6 mo. │ │ │ │

│ │ │ │ │ │ │ │

ENDENTATA: │ │ │ │ │ │ │ │

DASYPODIDÆ: │ │ │ │ │ │ │ │

Tatu novemcinctus,│ │ │ │ │ │ │ │

Nine banded │ ♀ │ │ │2 yrs.│Good │ 1,840.│ 10.│ 5.4

Armadillo │ │ │ │ │ │ │ │

│ │ │ │ │ │ │ │

MYRMECOPHAGIDÆ: │ │ │ │ │ │ │ │

Myrmecophaga │ │ │ │ │ │ │ │

tetradactyla, │ │ │ │ │ │ │ │

Tamandua Anteater │ ♀ │ │ │1 wk. │Good │ 3,300.│ 24.│ 7.3

│ │ │ │ │ │ │ │

MARSUPIALIA: │ │ │ │ │ │ │ │

DIDELPHYIDÆ: │ │ │ │ │ │ │ │

Didelphys │ │ │ │ │ │ │ │

virginiana, │ │ │ │ │ │ │ │

Common Opossum │ ♂ │ │ │2 wks.│Good │ 2,500.│ 6.5│ 2.6

Common Opossum │ │ │Young │3 mo. │Good │ 351.│ 6.│ 17.

│ │ │ │ │ │ │ │

DASYURIDÆ: │ │ │ │ │ │ │ │

Sarcophilus │ │ │ │ │ │ │ │

ursinus, │ │ │ │ │ │ │ │

Tasmanian Devil │ ♂ │ │Mature │4 yrs.│Thin │ 2,950.│ 8.│ 2.7

│ │ │ │6 mo. │ │ │ │

Dasyurus │ │ │ │ │ │ │ │

viverrinus, │ │ │ │ │ │ │ │

Common Dasyure │ ♀ │ │ │2 yrs.│Good │ 680.│ 4.5│ 6.6

│ │ │ │2 mo. │ │ │ │

Common Dasyure │ ♂ │ │ │8 mo. │Good │ 1,130.│ 5.5│ 4.8

Common Dasyure │ ♂ │ │ │1 yr. │Good │ 1,430.│ 7.│ 4.9

│ │ │ │6 mo. │ │ │ │

│ │ │ │ │ │ │ │

PHASCOLOMYIDÆ: │ │ │ │ │ │ │ │

Phascolomys │ │ │ │ │ │ │ │

mitchelli, │ │ │ │ │ │ │ │

Wombat. │ ♂ │ │Mature │9 yrs.│Excellent│ 25,900.│ 70.│ 2.7

│ │ │ │6 mo. │ │ │ │

│ │ │ │ │ │ │ │

MACROPODIDÆ: │ │ │ │ │ │ │ │

Macropus │ │ │ │ │ │ │ │

giganteus, │ │ │ │ │ │ │ │

Great Gray │ ♂ │ │Mature │3 yrs.│Good │ 34,000.│ 65.│ 1.9

Kangaroo │ │ │ │2 mo. │ │ │ │

Macropus rufus, │ │ │ │ │ │ │ │

Red Kangaroo │ ♂ │ │Mature │5 yrs.│Good │ 63,600.│ 70.│ 1.1

│ │ │ │8 mo. │ │ │ │

Macropus unguifer,│ │ │ │ │ │ │ │

Nailtailed │ ♂ │ │ │2 wks.│Good │ 4,600.│ 12.│ 2.6

Wallaby │ │ │ │ │ │ │ │

Macropus thetidis,│ │ │ │ │ │ │ │

Thigh striped │ ♂ │ │ │2 wks.│Good │ 5,150.│ 25.│ 4.8

Wallaby │ │ │ │ │ │ │ │

Macropus │ │ │ │ │ │ │ │

ualabatus, │ │ │ │ │ │ │ │

Black Wallaby │ ♀ │ │ │1 yr. │Good │ 8,170.│ 35.│ 4.2

│ │ │ │6 mo. │ │ │ │

Aepyprymnus │ │ │ │ │ │ │ │

rufescens, │ │ │ │ │ │ │ │

Rufous Rat │ ♀ │3 yrs.│Mature │3 yrs.│Good │ 1,130.│ 15.│ 13.3

Kangaroo │ │1 mo. │ │ │ │ │ │

Rufous Rat │ ♀ │6 yrs.│Mature │6 yrs.│Good │ 1,485.│ 15.│ 10.+

Kangaroo │ │9 mo. │ │9 mo. │ │ │ │

│ │ │ │ │ │ │ │

PASSERES: │ │ │ │ │ │ │ │

ICTERIDÆ: │ │ │ │ │ │ │ │

Quisculus │ │ │ │ │ │ │ │

quiscula, │ │ │ │ │ │ │ │

Purple Grackle │ ♂ │ │ │2 yrs.│Good │ 115.│ 2.7│ 23.4

│ │ │ │7 mo. │ │ │ │

Icterus icterus, │ │ │ │ │ │ │ │

Common Troupial │ ♂ │ │ │2 yrs.│Good │ 53.│ 2.│ 27.7

│ │ │ │7 mo. │ │ │ │

Common Troupial │ ♂ │ │ │4 yrs.│Thin │ 68.│ 2.│ 29.4

│ │ │ │7 mo. │ │ │ │

│ │ │ │ │ │ │ │

PLOCEIDÆ: │ │ │ │ │ │ │ │

Amadina │ │ │ │ │ │ │ │

erythrocephala, │ │ │ │ │ │ │ │

Red headed Finch│ ♀ │ │ │4 yrs.│Good │ 25.│ 1.2│ 48.

Munia malacca, │ │ │ │ │ │ │ │

Black headed │ ♂ │ │ │3 yrs.│Good │ 13.│ .7│ 52.6

Finch │ │ │ │ │ │ │ │

│ │ │ │ │ │ │ │

TANAGRIDÆ: │ │ │ │ │ │ │ │

Euphonia violacea,│ │ │ │ │ │ │ │

Violet Tanager │ ♀ │ │ │2 days│Good │ 15.│ 1.│ 66.6

Violet Tanager │ ♂ │ │ │2 days│Good │ 16.│ 1.│ 62.5

Tanagra cana, │ │ │ │ │ │ │ │

Silver blue │ ♂ │ │ │6 mo. │Good │ 29.│ 1.│ 34.5

Tanager │ │ │ │ │ │ │ │

Silver blue │ ♀ │ │ │1 yr. │Good │ 30.│ 1.│ 33.3

Tanager │ │ │ │2 mo. │ │ │ │

│ │ │ │ │ │ │ │

FRINGILLIDÆ: │ │ │ │ │ │ │ │

Zonotrichia │ │ │ │ │ │ │ │

albicollis, │ │ │ │ │ │ │ │

White throated │ ♂ │ │ │1 yr. │Good │ 35.│ 1.5│ 42.8

Sparrow │ │ │ │6 mo. │ │ │ │

White throated │ ♂ │ │ │6 mo. │Good │ 32.│ 1.5│ 46.9

Sparrow │ │ │ │ │ │ │ │

White throated │ ♂ │ │ │1 yr. │Good │ 23.│ 1.3│ 56.5

Sparrow │ │ │ │8 mo. │ │ │ │

Eophona melanura, │ │ │ │ │ │ │ │

Black tailed │ ♂ │ │ │2 mo. │Good │ 31.│ 2.│ 64.5

Hawfinch │ │ │ │ │ │ │ │

Black tailed │ ♂ │ │ │1 mo. │Good │ 30.│ 1.7│ 56.6

Hawfinch │ │ │ │ │ │ │ │

Java Sparrow │ ♂ │ │ │ │Good │ 28.│ 1.2│ 42.8

Passerina ciris, │ │ │ │ │ │ │ │

Nonpareil │ ♂ │ │ │9 mo. │Good │ 15.│ .5│ 33.3

Bunting │ │ │ │ │ │ │ │

Pipilo │ │ │ │ │ │ │ │

erythropthalmus, │ │ │ │ │ │ │ │

Towhee │ ♀ │ │ │1 yr. │Good │ 16.│ 1.2│ 75.

│ │ │ │2 mo. │ │ │ │

│ │ │ │ │ │ │ │

TURDIDÆ: │ │ │ │ │ │ │ │

Turdus iliacus, │ │ │ │ │ │ │ │

Red winged │ ♀ │ │ │5 yrs.│Good │ 55.│ 1.5│ 27.2

Thrush │ │ │ │6 mo. │ │ │ │

│ │ │ │ │ │ │ │

PITTIDÆ: │ │ │ │ │ │ │ │

Pitta strepitans, │ │ │ │ │ │ │ │

Noisy Pitta. │ │ │ │1 yr. │Good │ 92.│ 2.5│ 27.

│ │ │ │8 mo. │ │ │ │

│ │ │ │ │ │ │ │

CRATEROPODIDÆ: │ │ │ │ │ │ │ │

Garrulax │ │ │ │ │ │ │ │

leucolophus, │ │ │ │ │ │ │ │

White crested │ ♀ │ │ │2 yrs.│Good │ 105.│ 2.7│ 25.7

Jay Thrush │ │ │ │6 mo. │ │ │ │

│ │ │ │ │ │ │ │

PICARIÆ: │ │ │ │ │ │ │ │

RHAMPHASTIDÆ: │ │ │ │ │ │ │ │

Rhamphastos │ │ │ │ │ │ │ │

cuvieri, │ │ │ │ │ │ │ │

Cuvier’s Toucan │ ♀ │ │ │11 │Thin │ 356.│ 8.│ 22.4

│ │ │ │yrs. 9│ │ │ │

│ │ │ │mo. │ │ │ │

│ │ │ │ │ │ │ │

BUCEROTIDÆ: │ │ │ │ │ │ │ │

Lephoceros │ │ │ │ │ │ │ │

flavirostris, │ │ │ │ │ │ │ │

Yellow billed │ ♀ │ │ │1 yr. │Good │ 177.│ 6.│ 33.8

Hornbill │ │ │ │9 mo. │ │ │ │

│ │ │ │ │ │ │ │

STRIGES: │ │ │ │ │ │ │ │

ALUCONIDÆ: │ │ │ │ │ │ │ │

Aluco pratincola, │ │ │ │ │ │ │ │

Am. Barn Owl │ ♂ │ │ │1 mo. │Good │ 470.│ 11.│ 23.4

│ │ │ │ │ │ │ │

BUBONIDÆ: │ │ │ │ │ │ │ │

Bubo virginianus, │ │ │ │ │ │ │ │

Great Horned Owl│ ♀ │ │ │1 yr. │Good │ 1,415.│ 12.│ 8.4

Otus asio asio, │ │ │ │ │ │ │ │

Screech Owl │ ♂ │ │ │1 day │Good │ 122.│ 6.│ 49.

Strix varia varia,│ │ │ │ │ │ │ │

Barred Owl │ ♀ │ │ │11 │Good │ 1,022.│ 12.│ 11.6

│ │ │ │yrs. │ │ │ │

│ │ │ │ │ │ │ │

PSITTACI: │ │ │ │ │ │ │ │

PSITTACIDÆ: │ │ │ │ │ │ │ │

Conurus cactorum, │ │ │ │ │ │ │ │

Cactus conure │ ♀ │ │ │1 yr. │Good │ 64.│ 4.│ 62.5

│ │ │ │6 mo. │ │ │ │

Chrysotis │ │ │ │ │ │ │ │

leucocephala, │ │ │ │ │ │ │ │

White fronted │ │ │ │1 yr. │Good │ 251.│ 8.5│ 33.8

Amazon │ │ │ │ │ │ │ │

Chrysotis │ │ │ │ │ │ │ │

levaillanti, │ │ │ │ │ │ │ │

Levaillant’s │ │ │ │1 yr. │Good │ 300.│ 12.│ 40.

Amazon │ │ │ │ │ │ │ │

│ │ │ │ │ │ │ │

ACCIPITRES: │ │ │ │ │ │ │ │

SERPENTARIIDÆ: │ │ │ │ │ │ │ │

Serpentarius │ │ │ │ │ │ │ │

serpentarius, │ │ │ │ │ │ │ │

Secretary │ ♂ │ │ │2 wks.│Good │ 3,768.│ 15.│ 4.

Vulture │ │ │ │ │ │ │ │

│ │ │ │ │ │ │ │

FALCONIDÆ: │ │ │ │ │ │ │ │

Haliæetus │ │ │ │ │ │ │ │

leucocephalus, │ │ │ │ │ │ │ │

Bald Eagle │ ♀ │ │ │1 yr. │Good │ 2,860.│ 15.│ 5.2

│ │ │ │3 mo. │ │ │ │

│ │ │ │ │ │ │ │

COLUMBÆ: │ │ │ │ │ │ │ │

COLUMBIDÆ: │ │ │ │ │ │ │ │

Ocyphaps lophotes,│ │ │ │ │ │ │ │

Crested Pigeon │ │ │ │3 mo. │Thin │ 142.│ 2.│ 14.

Lophophaps │ │ │ │ │ │ │ │

leucogaster, │ │ │ │ │ │ │ │

Plumed Pigeon │ ♂ │ │ │ │Good │ 52.│ 1.2│ 23.

Phaps chalcoptera,│ │ │ │ │ │ │ │

Bronze winged │ ♀ │ │ │4 yrs.│Good │ 219.│ 1.5│ 6.8

Pigeon │ │ │ │2 mo. │ │ │ │

Columba phæonata, │ │ │ │ │ │ │ │

Dark backed │ ♂ │ │ │2 yrs.│Good │ 360.│ 2.│ 5.05

Pigeon │ │ │ │9 mo. │ │ │ │

Scardapella │ │ │ │ │ │ │ │

squamosa, │ │ │ │ │ │ │ │

Ground Dove │ ♀ │ │ │2 yrs.│Good │ 23.│ 1.7│ 64.

│ │ │ │9 mo. │ │ │ │

Zenaidura macroura│ │ │ │ │ │ │ │

carolinensis, │ │ │ │ │ │ │ │

Carolina Dove │ ♂ │ │ │2 yrs.│Thin │ 92.│ 1.│ 10.8

│ │ │ │9 mo. │ │ │ │

│ │ │ │ │ │ │ │

GALLI: │ │ │ │ │ │ │ │

PHASIANIDÆ: │ │ │ │ │ │ │ │

Coturnix │ │ │ │ │ │ │ │

pectoralis, │ │ │ │ │ │ │ │

Stubble Quail │ ♀ │ │ │2 yrs.│Good │ 70.│ .7│ 10.

Lophortyx │ │ │ │ │ │ │ │

californica │ │ │ │ │ │ │ │

californica, │ │ │ │ │ │ │ │

California Quail│ ♀ │ │ │1 yr. │Good │ 180.│ 1.5│ 8.33

│ │ │ │4 mo. │ │ │ │

Arboricola │ │ │ │ │ │ │ │

atrogularis, │ │ │ │ │ │ │ │

Black throated │ ♀ │ │ │1 yr. │Good │ 151.│ 2.5│ 16.

Hill Partridge │ │ │ │2 mo. │ │ │ │

Meleagris │ │ │ │ │ │ │ │

gallopavo │ │ │ │ │ │ │ │

silvestris, │ │ │ │ │ │ │ │

Eastern Wild │ ♂ │ │ │ │Good │ 6,340.│ 12.│ 1.9

Turkey │ │ │ │ │ │ │ │

│ │ │ │ │ │ │ │

CRACIDÆ: │ │ │ │ │ │ │ │

Ortalis vetula, │ │ │ │ │ │ │ │

Mexican Guan │ ♀ │ │ │2 yrs.│Thin │ 442.│ 5.│ 11.3

│ │ │ │2 mo. │ │ │ │

│ │ │ │ │ │ │ │

MEGAPODIDÆ: │ │ │ │ │ │ │ │

Catheturus │ │ │ │ │ │ │ │

lathami, │ │ │ │ │ │ │ │

Brush Turkey │ ♂ │ │ │3 mo. │Good │ 1,487.│ 5.│ 3.37

│ │ │ │ │ │ │ │

ALECTORIDES: │ │ │ │ │ │ │ │

GRUIDÆ: │ │ │ │ │ │ │ │

Grus lilfordi, │ │ │ │ │ │ │ │

Lilford’s Crane │ ♂ │ │ │1 yr. │Good │ 3,790.│ 18.│ 4.7

│ │ │ │4 mo. │ │ │ │

Tetrapteryx │ │ │ │ │ │ │ │

paradisea, │ │ │ │ │ │ │ │

Stanley Crane │ ♂ │ │ │3 yrs.│Good │ 4,450.│ 13.│ 2.9

│ │ │ │3 mo. │ │ │ │

│ │ │ │ │ │ │ │

STEGANOPODES: │ │ │ │ │ │ │ │

ANHINGIDÆ: │ │ │ │ │ │ │ │

Anhinga anhinga, │ │ │ │ │ │ │ │

Darter │ ♂ │ │ │3 yrs.│Good │ 251.│ 8.5│ 33.8

Darter │ ♀ │ │ │7 yrs.│Good │ 998.│ 6.│ 6.

│ │ │ │6 mo. │ │ │ │

│ │ │ │ │ │ │ │

HERODIONES: │ │ │ │ │ │ │ │

ARDEIDÆ: │ │ │ │ │ │ │ │

Nycticorax │ │ │ │ │ │ │ │

nyctanassa, │ │ │ │ │ │ │ │

Yellow crowned │ ♂ │ │ │1 yr. │Good │ 620.│ 7.│ 11.3

Night Heron │ │ │ │ │ │ │ │

│ │ │ │ │ │ │ │

CICONIIDÆ: │ │ │ │ │ │ │ │

Leptoptilus │ │ │ │ │ │ │ │

dubius, │ │ │ │ │ │ │ │

Adjutant Stork │ │ │ │ │ │ 7,873.│ 36.│ 4.5

Leptoptilus │ │ │ │ │ │ │ │

crumeniferus, │ │ │ │ │ │ │ │

Marabou Stork │ │ │ │ │ │ 4,580.│ 24.│ 5.2

│ │ │ │ │ │ │ │

PLATALEIDÆ: │ │ │ │ │ │ │ │

Carphibis │ │ │ │ │ │ │ │

spinicollis, │ │ │ │ │ │ │ │

Straw necked │ │ │ │ │ │ 1,665.│ 89.│ 4.8

Ibis │ │ │ │ │ │ │ │

│ │ │ │ │ │ │ │

PALAMEDES: │ │ │ │ │ │ │ │

Palmadea derbiana,│ │ │ │ │ │ │ │

Derbian Screamer│ ♂ │ │ │3 yrs.│Good │ 2,730.│ 10.│ 3.6

Derbian Screamer│ ♂ │ │ │1 wk. │Thin │ 1,700.│ 8.│ 4.7

│ │ │ │ │ │ │ │

ANSERES: │ │ │ │ │ │ │ │

ANATIDÆ: │ │ │ │ │ │ │ │

Cygnopsis │ │ │ │ │ │ │ │

cygnoides, │ │ │ │ │ │ │ │

Chinese Goose. │ ♂ │ │ │2 yrs.│Good │ 2,740.│ 15.│ 5.5

│ │ │ │6 mo. │ │ │ │

Plectropterus │ │ │ │ │ │ │ │

niger, │ │ │ │ │ │ │ │

Black Spurwinged│ ♂ │ │ │9 yrs.│Good │ 2,735.│ 13.│ 4.7

Goose │ │ │ │ │ │ │ │

Cereopsis novæ- │ │ │ │ │ │ │ │

hollandiæ, │ │ │ │ │ │ │ │

Cereopsis Goose │ ♀ │ │ │2 yrs.│Good │ 2,370.│ 9.│ 3.6

│ │ │ │3 mo. │ │ │ │

Cereopsis Goose │ ♂ │ │ │1 yr. │Good │ 2,748.│ 11.│ 4.

Anser domesticus, │ │ │ │ │ │ │ │

Sebastopol Goose│ ♂ │ │ │3 yrs.│Good │ 3,106.│ 19.│ 6.1

│ │ │ │2 mo. │ │ │ │

Anser fabalis, │ │ │ │ │ │ │ │

Bean Goose │ ♂ │ │ │12 │Good │ 2,640.│ 13.│ 4.9

│ │ │ │yrs. 6│ │ │ │

│ │ │ │mo. │ │ │ │

Chloephaga │ │ │ │ │ │ │ │

magellanica, │ │ │ │ │ │ │ │

Upland Goose │ ♂ │ │ │2 wks.│Thin │ 1,822.│ 8.│ 4.4

Coscoroba │ │ │ │ │ │ │ │

coscoroba, │ │ │ │ │ │ │ │

Coscoroba Swan │ ♂ │ │ │1 mo. │Good │ 1,915.│ 9.│ 4.7

Anas │ │ │ │ │ │ │ │

platyrhynchos, │ │ │ │ │ │ │ │

Mallard Duck │ ♀ │ │ │3 yrs.│Good │ 1,471.│ 8.│ 5.4

Mallard Duck. │ ♀ │ │ │3 yrs.│Good │ 525.│ 6.│ 11.4

Dafila acuta, │ │ │ │ │ │ │ │

Pintailed Duck. │ │ │ │3 yrs.│Good │ 489.│ 6.│ 12.2

Fuligula ferina, │ │ │ │ │ │ │ │

Pochard │ ♂ │ │ │4 yrs.│Good │ 600.│ 6.│ 10.

│ │ │ │6 mo. │ │ │ │

│ │ │ │ │ │ │ │

STRUTHIONES: │ │ │ │ │ │ │ │

STRUTHIONIDÆ: │ │ │ │ │ │ │ │

Struthio │ │ │ │ │ │ │ │

molybdophanes, │ │ │ │ │ │ │ │

Samoli Ostrich │ ♀ │ │ │9 yrs.│Thin │ 60,000.│ 37.│ .65

│ │ │ │3 mo. │ │ │ │

│ │ │ │ │ │ │ │

CASUARIIDÆ: │ │ │ │ │ │ │ │

Casuarius │ │ │ │ │ │ │ │

papuanus, │ │ │ │ │ │ │ │

Papuan Cassowary│ ♂ │ │ │8 yrs.│Good │ 24,000.│ 30.│ 1.3

────────────────────┴───┴──────┴───────────┴──────┴─────────┴────────┴──────┴──────

SECTION XIII-PART II

THE EYE

INFLAMMATIONS.

Conjunctivitis is rather rare but does occur in all varieties of

animals, seldom however, to the extent that the specimen has to be

sacrificed. So far as the daily reports can be relied upon we have had

no epidemic inflammations of the eye. The parrots and monkeys are the

only animals that can be handled enough for treatment, and in them the

applications have not seemed very efficacious. Two cases of

conjunctivitis and iritis have had a tuberculous basis and two other

specimens have had tuberculosis in the eye. Two parrots had, in

association with generalized tuberculosis, semisolid masses in the orbit

which dislocated the bulb, thickened the lids and presented as yellowish

granulating tumors under the conjunctiva; a Swainson’s long-tailed jay

(_Calocitta formosa_) had this lesion on both sides. The only case in a

mammal concerned an Anubis baboon (_Papio anubis_) in which one eye had

been enucleated, two weeks before death, for purulent ophthalmitis. The

other eye became affected shortly after the extraction and the animal

was killed; it was found to have caseous pneumonia. The tuberculous

process had probably begun in the region of the optic nerve and involved

the whole bulb. Secondary infection with pyogenic cocci had been

superimposed upon the original process. Keratomalacia, encountered on a

few occasions, will be discussed by Doctor White.

Iridocyclitis was found in a white browed guan (_Penelope

superciliaris_) the notes of which are condensed as follows:

The internal organs show nothing of value pathologically. The right

eye shows moderate conjunctivitis and a marked thickening of the

cornea with complete opacity. The lens is destroyed and the retina

infiltrated by gelatinous material. Humors are watery, non-

suppurative, but the fundal portion of the retina shows several poorly

circumscribed, yellowish white, gelatinous collections. Microscopical

section of cornea shows replacement of normal bundles by wavy ones

intermixed with small numbers of nuclei. These are never of

inflammatory type, but always of connective tissue type. Conjunctival

mucosa defective in centre, puckered but shows no subjacent

inflammatory features. Ciliary body richly infiltrated by lymphocytes

and vessels distinctly congested. This condition extends over whole

anterior surface of iris and for a short distance over posterior.

Sclera shows much bone formation. Chronic interstitial keratitis,

subacute interstitial iritis and cyclitis.

CATARACT.

Opacities of the cornea are quite common among our specimens, most often

due we believe, to local trauma; ungulates exhibit them more than other

varieties. Cataractous opacities of the lens are frequently observed in

senile animals but, while I have no figures for the statement, I believe

they are not as common among our specimens as can be observed in

domestic horses and dogs. No record has been made of streaky clouds or

spots in the lens but only of complete opacities. There are three only,

an aoudad (_Ovis tragelaphus_) a macaw (_Ara macao_) and a summer duck

(_Aix sponsa_) the last of which alone is interesting. This bird, a

fully developed adult female, was killed because of total blindness and

found to have a low grade chronic pancreatitis and a bilateral

Morgagnian cataract, the lens capsule containing a thin cloudy fluid

with the nucleus quite freely movable in it.

AMBLYOPIA.

A very interesting case of amblyopia in a young monkey was studied and

reported by Dr. H. M. Langdon and Doctor Cadwalader in the _Journal of

Comparative Pathology and Therapeutics_, Vol. XXVIII, Part 4. Because of

its unusual character and careful investigation, the report is

reproduced here:

Pigtailed macaque (_Macacus nemestrinus_) was born June 9, 1913, in

the monkey house, a well developed baby. He thrived and was as good as

any for his age. He was never known to have anything wrong with him

until on the morning of June 3, 1914, when he was found on the bottom

of the cage in the monkey house. He had clenched hands and feet, jaws

tightly closed, lips drawn back, eyes staring and glassy, with

convulsive shaking of the extremities. At intervals he would become

limp, with fists still clenched, and with only occasional jerks in the

extremities. This would last about a minute, and then convulsive

movements would be resumed. The entire “fit” lasted about ten minutes.

He was immediately removed from the large cage in the monkey house to

a small one in the back room of the laboratory. When put in the small

cage he staggered as if dazed, and groped about apparently blind. He

never recovered his sight entirely, but at times seemed to see better

than at others. He was not seen in a “fit” in the laboratory. On June

24th, a small piece of banana was offered by a person who stood

directly in the sunlight. The monkey came to the front of the cage,

reached out and grasped very firmly the thumb of the hand holding the

banana but did not take the banana although he very plainly wanted it.

The banana was thrown into the cage, hitting the monkey on the back.

He turned very quickly, then smelled over the floor of the cage until

he found the banana. On June 30th, he was examined by Doctor Langdon

and the following condition was noted:

“Pupils react to the light of the ophthalmoscope. Optic discs are

normal. Arteries possibly a little small. No other fundus changes.” On

July 1, a cloudy day, he was laid facing a window. A coat sleeve was

laid over his eyes for a minute and then quickly removed. His pupils

were seen to react slowly but distinctly to the light. His gaze would

not follow a finger moved in front of his eyes. When put back in the

cage he climbed up on the wire at the back and then tried to climb the

plain sheet-iron side. He groped and felt for a support and then fell.

This he did several times. About August 1, when the eyes were

examined, there seemed to be more visual perception and very

distinctly prompter pupillary reflex, which condition remained about

the same when examined October 1. He died October 10, 1914, of a

compound fracture of the right femur inflicted by a monkey in the

adjoining cage.

At autopsy the viscera appeared normal throughout. The animal was

fairly well nourished. There was about 5 cc. clear, pale yellow fluid

under the dura. It escaped upon removal of the brain. There were

adhesions of the dura over the temporal lobe (inferior surface),

posterior and external to the optic tract, so firm as to remove some

periosteum and superficial bone. Rest of dura seemed normal.

Examination of the brain. Sections were made from different parts of

the cerebral cortex, all of which were more or less alike. There was

swelling of the endothelium of the pial lymph spaces, with some

separation of the fibres of the pia itself which extended into the

sulci. The perivascular lymph spaces of the larger arteries of the

cortex were dilated, and the adjacent cerebral tissue was edematous. A

well marked endothelial swelling and hyperplasia affected a number of

the arteries and capillaries producing marked general or nodular

thickening in some places. Accompanying these hyperplastic changes

there was a marked calcification of some of the arteries. This was not

confined to one tunic, but in some instances it extended almost

completely through the vessel wall, and here and there the lumen of a

vessel was nearly obliterated. The main features were endothelial

hyperplasia, edema of the pia and of the subpial cortex with some

calcification of the vessels. It was perhaps less well marked in the

occipital lobes than in other parts. The optic nerve and other

portions of the brain appeared to be normal.

MOON BLINDNESS.

It seems also profitable to repeat here a report Dr. H. M. Langdon and I

made in 1911 upon a horse with periodic ophthalmia or “moon blindness,”

a widespread condition and one upon which there is even to-day little

known and much contradictory theorizing. It is worthy of record that Dr.

J. H. W. Eyre of Guy’s Hospital, had a case to study at the same time as

ours. He did not find the protozoön-like body discussed below, but laid

weight upon the isolation of St. aureus, an organism often mentioned in

the literature about this disease. I cite the whole report since our

publication in the 1911 Report of this Garden seems not to have been

quoted in any of the reference articles on “Moon blindness.” Those who

are interested in the clinical and pathological sides of the question

will find a good summary in _Veröff. aus der-Jahres. Vet. Berichten der

beamt. Tierärzte Preussens_, 1908, and the bacteriology of the equine

eye by Karsten, _Inaug. Disser._ Giessen, 1909.

“During the latter part of 1909 and first part of 1910 we had a horse

referred to us suffering with recurrent ophthalmia or moon blindness.

This affection, suggested by its name, is supposed to have some relation

to the lunar periods. Some points in our work showed that such may be

the case. Attacks appear not infrequently at the time of the full moon,

and in our only experimental infection twenty-eight days elapsed between

inoculation and a general ocular inflammation.

“This affection manifests itself as a conjunctivitis early in the

attack, but rapidly progresses to an iridocyclitis and lastly to a

panophthalmitis. After each attack the ball is smaller until it is so

shrunken as to be sightless from chronic thickening and opacities. The

causation is not known. The disease behaves not unlike an infectious

one, remaining in a stud for years at a time. Not every horse may be

affected. It has been connected with dampness, bad fodder, overwork and

the like. Again others have connected it with malaria or rheumatism.

Potapenke, Vigezzi, Koch and others have found various microörganisms,

no two of which seem to be the same. Even an animal organism like

malaria has been described. (Whether or not malaria has anything to do

with the disease, it must be said that our horse was favorably affected

in regard to temperature as well as to the eye condition by repeated

subcutaneous injections of Quinine Bisulphate, Grain xx daily.) The

attacks last five to nine days. One or both eyes may be attacked and not

uncommonly do they alternate. One eye may cease to have attacks while

the other continues. The experiments here recorded were made with the

idea of transmitting the disease to other horses. They were only

partially successful. During eight months the affected animal referred

to us had six attacks of ophthalmia. The attack was observed for study

on the first occasion, but during the second his anterior chamber was

entered by a needle attached to a syringe, the exudate aspirated and

injected into the eye of a horse with apparently healthy eyes. The

history of this second horse will be given later. The attacks of the

first horse ranged from six to twelve days. Five of the six affected the

left eye and one the right. In January, 1910, the left eye was used for

further inoculation, and following this traumatism complete recovery

never took place. The corneal scar left by the needle tract almost

disappeared, but an inferior anterior synechia formed and was followed

by a spreading opacity of the cornea, much wrinkling of the iris and

opacity of the depths. After the fourth attack in this eye it was

completely blind. Material was obtained from this eye during its last

attack, but it was merely serous fluid containing a few blood cells and

epithelium, but no bacteria.

“In transferring the affection from this animal, the conjunctival sac

was washed with 1–5000 bichloride of mercury solution and well rinsed

with salt solution. The anterior chamber was then entered with an

aspirating needle and the exudate removed. This consisted of 0.4 cc.

slightly turbid straw colored fluid containing a few shreds of lymph.

Bacteriological cultures, moist and dry preparations were made from a

part of this, while the remainder was introduced into the anterior

chamber of the second horse. This animal’s eye showed the effects of the

traumatism for eight days, and then was normal save for a small opaque

spot in the cornea left from needle puncture. After twenty-three days a

small patch of lymph collected in the pupil. This increased slowly

accompanied by lacrymation until the twenty-seventh day, when a sudden

and violent conjunctivitis arose. The lymph in the anterior chamber

likewise suddenly increased and rapidly became pus, forming a hypopyon.

The conjunctivitis became purulent. The violent stage lasted five days

and slowly subsided, leaving an ectropion with a densely injected bulbar

conjunctiva, almost complete corneal opacity and an irregular

contraction of iris, apparently due to several small synechiæ. The

depths could not be seen because of the corneal condition. This stage of

affairs remained during the rest of the animal’s life, two months. He

was permitted to live to see if an exacerbation of this chronic process

or involvement of the other eye would appear. Such not occurring in two

months, he was killed and the eyes removed. Fluid removed from the left

eye of the first horse when killed during the last attack was injected

into the anterior chamber of a third horse. This animal’s eye received

the operation well and the trauma had entirely disappeared when the

animal died on the eighth day.

“LABORATORY EXAMINATIONS.—From fluid removed from horse eye (No. 1)

anaerobic cultures made on milk and blood serum, blood agar, glycerine

agar; cultures were made directly from the fluid, while the coagula were

dried upon slides and stained as follows: Loeffler’s, Gram’s, Giemsa. In

all there are very few recognizable bodies. They are red blood cells,

polynuclears and a very few small mononuclear cells. In regard to

microörganisms three structures present themselves. A well staining

Gram-positive, rounded end rod of fairly uniform size but tending to

grow in pairs and stain rather irregularly with Loeffler and Giemsa.

These forms are sometimes called ‘dumbbell’ in that they are bipolar, or

even seem to have a constriction in their centre. Another form is

peculiar and cannot be said to be recognized as a bacterium. It is

circular, of fairly regular size and contour and in many places looks

like a very large coccus. In Loeffler’s stain it is colored deeply in

the centre with a paler marginal zone and an unstained halo about it,

which, however, is not like a capsule. In the Gram and Giemsa method it

is deeply blue or purple with a retractile centre and very sharply

outlined contour. These forms varied from 3 to 5 microns. The third form

is a wavy delicate short mycelium-like thread. Smears from the cultures

as made above showed chiefly a Gram-positive, rounded end rod but which

did not grow on planting out. It grew on aerobic media, but was not

found on anaerobic. The Gram-positive organism would not grow beyond the

fourth generation. It was not identified with any known species by the

characters manifested during the short time we were able to keep it

alive but could be placed in the Hog Cholera group. The mycelium was

found to be an aspergillus. In regard to the large coccus-like body,

little can be added to the above description. Further examination did

not reveal characters permitting us to place it among the protozoa. No

evidences of division were seen. The body is quite uniform in

appearance, varying only in size. Whatever this is it seems to be an

organized body.”

“Cultures from pus in the anterior chamber of the second horse showed

the palely staining rod, an aspergillus and Micrococcus aquatilis. The

first was planted on horse serum bouillon, but did not grow after the

first generation. These cultures were made after death, but the cultures

made during the acute attack direct from conjunctival sac contained such

a host of organisms that no judgment could be formed of their relative

importance. The polar staining rod was found in smears. No large coccus-

like bodies were observed in the second horse. Fluid taken from the

first horse’s eye at death was sterile.”

“These observations are at variance with those of others but such

results are not unique in this respect. It seems as if the polar

staining rod deserves some consideration, and we expect to devote some

attention to it if another horse suffering from recurrent ophthalmia

come to our notice. The large coccus-like bodies are very interesting

and may be protozoa. The finding of the amœba in the cases of Potapenke,

increases their importance. Before, during and after the fourth attack

of the first horse twenty grains of quinine bisulphate were given

hypodermically daily for twenty days. The attack was very mild. Before

the drug was given his temperature had ranged from 99° to 101° F.

Immediately after the first dose the temperature fell to below 99° F.,

and remained at a very regular level during the entire twenty days. No

malarial organisms were found in the blood.”

The ear is without special interest except as a place of localization of

sarcoptes, demodex and fly larvæ. A few cases of acute catarrhal otitis

media have been found in association with nasopharyngitis both of the

nonspecific variety and that which resembles distemper. One case which

led to meningitis has been mentioned.

Disease in captive wild mammals and birds · 第 7 / 13 章