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Agricultural Zoology · J. Ritzema Bos — chapter 4 of 30 · ~1,632 words · public domain

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In all other Vertebrates a more rapid movement of the blood is rendered possible by the insertion of a second heart, quite similar in every respect to the other heart, in the course of the blood between the respiratory organs and the body. The first heart drives the blood through the lung capillaries, and therefore corresponds to the fish-heart; from these capillaries the blood returns to the auricle of the second heart, and from the ventricle of that heart travels to the various parts of the body. When it has completed this course, it returns to the auricle of the first heart. Although these two structures work independently, they lie close together and make up a single organ. We do not therefore speak of two individual hearts, but of one heart with two halves. The first half, which receives the blood, poor in oxygen, that is returned from the body, and sends it on to the lungs, lies on the right, and is termed the right half. The second half, which receives the richly oxygenated blood from the lungs, and pumps it to the various parts of the body, is termed the left half (Fig. 9 and explanation).

In the arrangement just described, which is found in Mammals and Birds, the blood returning from the lungs is propelled with new force through the body, and therefore circulates very quickly, so that the various parts receive a relatively large amount of oxygen in a short time. It is therefore intelligible that Birds and Mammals develop more warmth than Fish. They possess a special, constant body temperature, somewhat different in different species, but usually lying between 98° and 104° Fhr., and they are called warm-blooded animals.

FIG. 9.—Diagram of the Mammalian Heart. 1, right, 2, left ventricle; 3, right, 4, left auricle; 5, superior, 6, inferior vena cava; 7, pulmonary artery forking into branches for right and left lungs; 8, the four pulmonary veins; 9, the great body-artery (aorta); the arrows indicate the direction of the blood-stream. ]

FIG. 10.—Diagram of the Heart of a Reptile. Between the right (r.K.) and left (l.K.) ventricles is a perforated partition. r.V.K., right auricle; l.V.K., left auricle; H.v., vena cava, carrying back the blood which has traversed the body into the right auricle; L.art., pulmonary artery; L.v., pulmonary vein; Ao., aorta. ]

In Reptiles (snakes, lizards, etc.), the two halves of the heart are not entirely distinct, since there is an opening in the partition-wall between the two ventricles. As a consequence of this, the poorly oxygenated blood of the right half of the heart mixes with the richly oxygenated blood of the left half, the extent to which this mixing takes place being proportional to the size of the aperture. In Reptiles, therefore, the blood supplied to the lungs is not so poor in oxygen as it might be, nor, on the other hand, is the blood supplied to the other parts of the body completely oxygenated. As consequences of this: (1) respiration is feebler, and (2) the development of heat less than in Mammals and Birds (i.e. reptiles are cold-blooded), and (3) the chemical changes taking place in the body (the metabolism) go on more slowly than in warm-blooded animals, and we can understand why reptiles execute fewer movements in a given space of time.

FIG. 11.—Diagram of a Frog’s Heart. (The ventricle K. is quite undivided: compare Figs. 9 and 10.) Other letters as in Fig. 10. ]

In Amphibians (e.g. frog) the two ventricles are similarly connected, but the opening is still larger than in Reptiles, and the partition-wall may even be altogether absent. It follows, therefore, that the mixing of the two kinds of blood is still more complete, and that Amphibians, too, are cold-blooded.

The vertebrate sub-kingdom embraces the classes of I. Mammals; II. Birds; III. Reptiles; IV. Amphibians; V. Fishes.

CLASS I.: =MAMMALIA= (SUCKLERS).

Warm-blooded Vertebrates (p. 16), usually covered with hair, and bringing forth living young, that suck for some time after birth. The female is provided with milk-glands on the thorax or abdomen, or both those regions.

Speaking quite broadly, the skeleton is like that of man, described on pp. 4–8. There are, however, great differences in detail. The cranium is relatively much smaller, and the bones of the face (especially of the jaws) are usually much larger than in the human skull. The number of the cervical vertebræ is seven in all Mammals, as in man; but the other kinds of vertebræ vary in number in the different species. The number of caudal vertebræ, for example, is very variable. As most Mammals go on all fours, their fore and hind limbs are much more similar than is the case in man. In many the thigh and upper-arm bones are drawn closely up to the body (horse, ox, pig). Mammals never have more than five fingers or toes, but may have fewer. The thumb or great toe is the first to disappear (hind foot of dog, fore and hind foot of pig). There may be only three (rhinoceros), two (ox, sheep), or one (horse) digit developed. In addition to fully developed digits, there are in many Mammals very small stunted ones (“dew-claws” of the stag).

FIG. 12.—Vertical Section of a Human Grinding Tooth. ]

FIG. 13.—Crown of a Grinder of the Ox. a, cement; b, enamel; c, dentine; d, enamel; e, cement. ]

There are also great differences in the way of resting the feet on the ground. Man and bear tread on the soles of the feet (plantigrade); dog and cat walk on the under side of the toes (digitigrade), not on the other parts of the feet. Ox, pig, horse, etc., rest while walking only on the tips of the toes, which are sheathed in hoofs (unguligrade).

The teeth of mammals are wedged into special sockets in the jaw-bones. The structure of a mammalian tooth is made clear by Fig. 12. We first distinguish a pulp-cavity (p), which in the living animal is filled with a substance supplied by a bloodvessel and nerve. This cavity is surrounded by the dentine (d), a hard substance which makes up the greater part of the tooth. Hard enamel (s) covers the whole of the crown in man and many animals, while in certain other forms it is found only on part of the crown. The root of the tooth is covered with cement (z), a bone-like substance.

All teeth in which the entire surface of the crown is covered by enamel only are known as simple teeth, while those into which the enamel only penetrates in more or less deep folds, leaving the rest of the crown uncovered, are known as compound teeth (Fig. 13). The structure of the teeth is related to the nature of the food. We distinguish three kinds of teeth in the same animal, which, however, are not all present in every species; these are the incisors, canines, and grinders. The first two kinds are changed; but only the anterior grinders, known as the premolars, are changed, while the hinder ones, the true molars, do not first appear as “milk” teeth, but rather later on with the other “permanent” teeth.

The following orders of Mammals are distinguished: I. Bimana (Man), II. Quadrumana (Apes), III. Carnivora (Beasts of prey), IV. Insectivora (Insect-eaters), V. Cheiroptera (Bats), VI. Rodentia (Gnawers), VII. Ruminantia, VIII. Solidungula, IX. Pachydermata, X. Cetacea, XI. Edentata, XII. Marsupialia (Pouched animals), XIII. Monotremata.

I shall deal here only with those orders which are of agricultural importance.

ORDER: =Carnivora= (BEASTS OF PREY).

In each jaw there are six relatively small incisor teeth; and, on each side of these, a large projecting canine, by which the flesh is torn from the body of the prey (Fig. 14). The premolars and the first of the true molars (the carnassials) are strongly compressed, and have a cutting crown; their outer surface is completely covered with hard enamel. As the lower jaw is smaller than the upper jaw, and is only able to move up and down, not from side to side, the sharp crowns of the premolars, and especially those of the large carnassials, cut along one another, and divide anything coming between them as if with shears. The small molars which are usually found behind the carnassials have broad tuberculated crowns. The temporal (i.e. chewing) muscles are strongly developed, the general result of which is that the head is broad. The claws are very sharp in some of the families. The Carnivora are powerful animals, move very quickly, and are endowed with keen smell and sight.

Footnote 2:

The upper carnassials = last premolars. The lower „ = first molars.—TR.

The wild Carnivora living in Britain belong to the families of cats, dogs, and weasels.

Family: =Felidæ= (Cat Family).

Typical Carnivora with very large canines and carnassials, two premolars in each half of each jaw, one of the upper molars, but none of the lower ones, small and tuberculated. Tongue rough. Fore and hind feet five-toed. When not in use, the claws are drawn back (retracted). The Felidæ are digitigrade. Backbone very flexible, and with free power of movement. The Felidæ are bloodthirsty, nocturnal animals, many of which climb well, and spring upon their prey.

The group is specially exemplified by the =Domestic Cat=, the parent stock of which is the Nubian cat (Felis maniculata), a native of Nubia and the Soudan. The =Wild Cat= (Felis catus) is larger than the common kind, and has a thicker tail. Formerly it was tolerably common in Britain, but now only occurs in a few thinly populated districts.

FIG. 14.—Skull of Domestic Cat. ]

The =Lynx= (Felis Lynx), found at one time in Germany, still lives in the Carpathians, and in Switzerland, but occurs more commonly in Scandinavia, Denmark, and Russia.

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