the Fourth Week of Advent
Click here to join the effort!
Bible Encyclopedias
Horse
1911 Encyclopedia Britannica
or (a word common to Teutonic languages in such forms as hors, hros, ros; cf. the Ger. ross), a name properly restricted to the domesticated horse (Equus caballus) and its wild or halfwild representatives, but in a zoological sense used as a general term for all the members of the family Equidae.
Species The distinctive characteristics of the family, and its position in the zoological system, are given in the articles Equidae and Perissodactyla. Here attention is concentrated on the leading features of the horse as contrasted with the other members of the same family, and subsequently on the anatomical structure of the former animal. The evolution of the existing representatives of the family from primitive extinct animals is summarized in the article Equidae.
Horse, Wild Horse, Pony. - The horse (Equus caballus) is distinguished from the others by the long hairs of the tail being more abundant and growing quite or nearly from the base as well as the end and sides, and also by possessing a small bare callosity on the inner side of the hind leg, just below the "hock" or heel joint, in addition to the one on the inner side of the fore-arm above the carpus or " knee," common to all the genus. The mane is also longer and more flowing, and the ears are shorter, the limbs longer, and the head smaller.
Though existing horses are usually not marked in any definite manner, or only irregularly dappled, or spotted with light surrounded by a darker ring, many examples are met with showing a dark median dorsal streak like that found in all the other members of the genus, and even with dark stripes on the shoulders and legs.
Two distinct types of horse, in many instances largely modified by interbreeding, appear to exist. (I) The northern, or dun type, represented by the dun ponies of Norway (Equus caballus typicus), the closely allied Celtic pony (E. c.celticus) of Iceland, the Hebrides, &c., and the wild pony of Mongolia (E. c. przewalskii), with which the now extinct tarpan of the Russian steppes appears to have been identical. The prevalent colour is yellowdun, with dark brown or black mane, tail and legs; in the wild forms the muzzle is often white and the root of the tail shorthaired; while the head is relatively large and heavy. No depression exists in the skull in front of the eye. Most of the ordinary horses of N.W. Europe are descended from the dun type; with more or less admixture of Barb blood. (2) The southern, or Barb type, represented by Barbs, Arabs, thoroughbreds, &c. (E. c. asiaticus or libycus), in which the typical colour is bay with black " points " and often a white star on the forehead, and the mane and tail are long and full. The skull generally shows a slight depression in front of the socket of the eye, which, although now serving as the attachment for the muscle running to the nostril, may represent the face-gland of the extinct Hipparion. Many of the dark-coloured horses of Europe have Barb or Arab blood in their veins, this being markedly the case with the Old English black or Shire horse, the skull of which shows a distinct depression in front of the eye-socket. This depression is still more marked in the extinct Indian E. sivalensis, which may have been the ancestral form.
In Europe wild horses were abundant in the prehistoric Neolithic or polished-stone period. Judging from the quantity of their remains found associated with those of the men of that time, the chase of these animals must have been among man's chief occupations, and horses must have furnished him with one of his most important food-supplies. The characters of the bones preserved, and certain rude but graphic representations carved on bones or reindeers' antlers, enable us to know that they were rather small in size and heavy in build, with large heads and rough shaggy manes and tails, much like, in fact, the recently extinct tarpans or wild horses of the steppes of the south of Russia, and the still-surviving Mongolian wild pony or " Przewalski's horse." These horses were domesticated by the inhabitants of Europe before the dawn of history. Horses are now diffused by the agency of man throughout almost the whole of the inhabited parts of the globe, and the great modifications they have undergone in consequence of domestication, crossing, and selective breeding are well exemplified by comparing such extreme forms as the Shetland pony, dwarfed by uncongenial climate, the thoroughbred racer, and the London dray-horse. In Australia, as in America, horses imported by European settlers have escaped into unreclaimed lands and multiplied to a prodigious extent, roaming in vast herds over the wide and uncultivated plains.
Ass, Zebra, Quagga
The next group is formed by the Asiatic wild asses, or kiangs and onagers, as they might well be called, in order to distinguish them from tl}e wild asses of Africa. These asses have moderate ears, the tail rather long, and the back-stripe dark brown and running from head to tail. On the neck and withers this stripe is formed by the mane. There are two species of Asiatic wild ass, with several varieties. The first and largest has two races, the chigetai (Equus hemionus) of Mongolia, and the kiang (E. h. kiang) of Tibet; which is a redder animal. The onager (E. onager), of which there are several races, is smaller, with a broader dorsal stripe, bordered with white; the colour varying from sandy to greyish. This species ranges from Baluchistan and N.W. India to Persia, Syria and Arabia. These asses inhabit desert plains or open table-land; the kiang dwelling at elevations of about 14,000 ft. They are generally found in herds of from twenty to forty, although occasionally in larger numbers. All are fleet, and traverse rough ground with speed. On the lowlands they feed on dry grasses, and in Tibet on small woody plants. In India and Persia they are difficult to approach, although this is not the case in Tibet. Their sandy or chestnut colouring assimilates them to the horse, and separates them widely from the African wild asses, which are grey. The kiang has also larger and more horse-like hoofs, and the tail is haired higher up, thus approximating to Equus caballus przewalskii. Among the striped species, or zebras and quaggas of Africa, the large Grevy's zebra (Equus grevyi) of Somaliland and Abyssinia stands apart from the rest by the number and narrowness of its stripes, which have an altogether peculiar arrangement on the hind-quarters, the small size of the callosities on the fore-legs, the mane extending on to the withers and enormous rounded ears, thickly haired internally. The large size of the ears and the narrow stripes are in some degree at any rate adaptations to a life on scrub-clad plains.
Next comes the closely allied species with small pointed ears, of which the true quagga (E. quagga) of South Africa is now extinct. This animal has the dark stripes limited to the .head, neck and shoulders, upon a brown ground. In the typical form, now also extinct, of the bonte-quagga, dauw, or Burchell's zebra (E. burchelli), the ground-colour is white, and the stripes cover the body and upper part of the limbs. This was the commonest species in the great plains of South Africa, where it roamed in large herds, often in company with the quagga and numerous antelopes. The species ranges from the Orange river to the confines of Abyssinia, but its more northern representatives show a gradual increase in the striping of the legs, culminating in the north-east African E. burchelli granti, in which the stripes extend to the hoofs. The markings, too, are alternately black and white, in place of brown and creamy, with intermediate " shadow stripes," as in the southern races.
Lastly, there is the true or mountain zebra (E. zebra), typically from the mountain ranges of Cape Colony, where it is now specially protected, but represented by E. zebra penricei in south-west Africa. In its relatively long ears and general build it approaches the African wild asses, from which it chiefly differs by the striping (which is markedly different from that of the quagga-group) and the reversal of the direction of the hairs along the spine.
The African wild ass (E. asinus) is the parent of the domesticated breed, and is a long-eared grey animal, with no forelock, and either a shoulder-stripe or dark barrings on the legs. There are two races, of which the Nubian E. a. africanus is the smaller, and has a continuous dorsal stripe and a shoulder-stripe but no bars on the legs. The Somali race (E. a somaliensis), on the other hand, is a larger and greyer animal, with an interrupted dorsal and no shoulder-stripe, but distinct leg-barrings.
Hybrids
There are thus eight modifications of the horse-type at present existing, sufficiently distinct to be reckoned as species by most zoologists, and easily recognizable by their external characters. They are, however, all so closely allied that'each will, at least in a state of domestication or captivity, breed with any of the others. Cases of fertile union are recorded between the horse and the quagga, the horse and the bonte-quagga or Burchell's zebra, the horse and the onager and kiang or Asiatic wild asses, the common ass and the zebra, the ass and bontequagga, the ass and the onager, the onager and the zebra, and the onager and the bonte-quagga. The two species which are farthest removed in structure, the horse and the ass, produce, as is well known, hybrids or mules, which in certain qualities useful to man excel both their progenitors, and in some countries and for certain kinds of work are in greater requisition than either. Although occasional more or less doubtful instances have been recorded of female mules breeding with the males of one or other of the pure species, it is more than doubtful if any case has occurred of their breeding inter se, although the opportunities of doing so must have been great, as mules have been reared in immense numbers for at least several thousands of years. We may therefore consider it settled that the different species of the group are now in that degree of physiological differentiation which enables them to produce offspring with each other, but does not permit of the progeny continuing the race, at all events unless reinforced by the aid of one of the pure forms.
The several members of the group show mental differences quite as striking as those exhibited by their external form, and more than perhaps might be expected from the similarity of their brains. The patience of the ass, the high spirit of the horse, the obstinacy of the mule, have long been proverbial. It is very remarkable that, out of so many species, two only should have XIII. 2 3 a shown any aptitude for domestication, and that these should have been from time immemorial the universal and most useful companions and servants of man, while all the others remain in their native freedom to this day. It is, however, still a question whether this really arises from a different mental constitution causing a natural capacity for entering into relations with man, or whether it may not be owing to their having been brought gradually into this condition by long-continued and persevering efforts when the need of their services was felt. It is possible that one reason why most of the attempts to add new species to the list of our domestic animals in modern times have ended in failure is that it does not answer to do so in cases in which existing species supply all the principal purposes to which the new ones might be put. It can hardly be expected that zebras and bontequaggas fresh from their native mountains and plains can be brought into competition as beasts of burden and draught with horses and asses, whose useful qualities have been augmented by the training of thousands of generations of progenitors.
Not infrequently instances occur of domestic horses being produced with a small additional toe with complete hoof, usually on the inside of the principal toe, and, though far more rarely, three or more toes may be present. These malformations are often cited as instances of reversion to the condition of some of the earlier forms of equine animals previously mentioned. In some instances, however, the feet of such polydactyle horses bear little resemblance to those of the extinct Hipparion or Anchitherium, but look rather as if due to that tendency to reduplication of parts which occurs so frequently as a monstrous condition, especially among domesticated animals, and which, whatever its origin, certainly cannot in many instances, as the cases of entire limbs superadded, or of six digits in man, be attributed to reversion.
Anatomy The anatomical structure of the horse has been described in detail in several works mentioned in the bibliography at the end of this section, though these have generally been written from the point of view of the veterinarian rather than of the comparative anatomist. The limits of the present article will only admit of the most salient points being indicated, particularly those in which the horse differs from other Ungulata. Unless otherwise specified, it must be understood that all that is stated here, although mostly derived from observation upon the horse, applies equally well to the other existing members of the group.
Skeleton
The skull as a whole is greatly elongated, chiefly in consequence of the immense size of the face as compared with the hinder or true cranial portion. The basal line of the cranium from the lower border of the foramen magnum to the incisor border of the palate is nearly straight. The orbit, of nearly circular form, though small in proportion to the size of the whole skull, is distinctly marked, being completely surrounded by a strong ring of bone with prominent edges. Behind it, and freely communicating with it beneath the osseous bridge (the post-orbital process of the frontal) forming the boundary between them, is the small temporal fossa occupying the whole of the side of the cranium proper, and in front is the great flattened expanse of the " cheek," formed chiefly by the maxilla, giving support to the long row of cheek-teeth, and having a prominent ridge running forward from below the orbit for the attachment of the masseter muscle. The lachrymal occupies a considerable space on the flat surface of the cheek in front of the orbit, and below it the jugal does the same. The latter sends a horizontal or slightly ascending process backwards below the orbit to join the under surface of the zygomatic process of the squamosal, which is remarkably large, and instead of ending as usual behind the orbit, runs forwards to join the greatly developed post-orbital process of the frontal, and even forms part of the posterior and inferior boundary of the orbit, an arrangement not met with in other mammals. The closure of the orbit behind distinguishes the skull of the horse from that of its allies the rhinoceros and tapir, and also from all of the perissodactyles of the Eocene period. In front of the brain cavity, the great tubular nasal cavities are provided with well-developed turbinal bones, and are roofed over by large nasals, broad behind, and ending in front in a narrow decurved point. The opening of the anterior nostrils is prolonged backwards on each side of the face between the nasals and the elongated slender premaxillae. The latter expand in front, and are curved downwards to form the semicircular alveolar border which supports the large incisor teeth. The palate is narrow in the interval between the incisor and molar teeth, in which are situated the large anterior palatine foramina. Between the molar teeth it is broader, and it ends posteriorly in a rounded excavated border opposite the hinder border of the penultimate molar tooth. It is mainly formed by the maxillae, as the palatines are very narrow. The pterygoids are delicate slender slips of bone attached to the hinder border of the palatines, and supported externally by, and generally welded with, the rough pterygoid plates of the alisphenoid, with no pterygoid fossa between. They slope obliquely forwards, and end in curved, compressed, hamular processes. There is a distinct alisphenoid canal for the passage of the internal maxillary artery. The base of the cranium is long and narrow; the alisphenoid is very obliquely perforated by the foramen rotundum, but the foramen ovale is confluent with the large foramen lacerum medium behind. The glenoid surface for the articulation of the mandible is greatly extended transversely, concave from side to side, convex from before backwards in front, and hollow behind, and is bounded posteriorly at its inner part by a prominent post-glenoid process. The squamosal enters considerably into the formation of the temporal fossa, and, besides sending the zygomatic process forwards, it sends down behind the meatus auditorius a post-tympanic process which aids to hold in place the otherwise loose tympano-periotic bone. Behind this the exoccipital gives off a long paroccipital process.
FIG. I. - Side view of Skull of Horse, with the bone removed so as to expose the whole of the teeth.
PMx, Premaxilla. c, The canine tooth.
Mx, Maxilla. pm', The situation of the rudi Na, Nasal bone. mentary first premolar, Ma, Jugal or malar bone. which has been lost in L, Lacrymal bone. the lower, but is present Fr, Frontal bone. in the upper jaw.
Sq, Squamosal bone. pmt, p m 3, and pm', The three Pa, Parietal bone. fully developed pre oc, Occipital condyle. molar teeth.
pp, Paroccipital process. m', m 2, and m 3, The three true and The three incisor teeth. molar teeth.
The periotic and tympanic are welded together, but not with the squamosal. The former has a wide but shallow floccular fossa on its inner side, and sends backwards a considerable " pars mastoidea," which appears on the outer surface of the skull between the posttympanic process of the squamosal and the exoccipital. The tympanic forms a tubular meatus auditorius externus directed outwards and slightly backwards. It is not dilated into a distinct bulla, but ends in front in a pointed rod-like process. It completely embraces the truncated cylindrical tympanohyal, which is of great size, corresponding with the large development of the whole anterior arch of the hyoid. This consists mainly of a long and compressed stylohyal, expanded at the upper end, where it sends off a triangular posterior process. The basi-hyal is remarkable for the long, median, pointed, compressed " glossohyal " process, which it sends forward from its anterior border into the base of the tongue. A similar but less developed process is found in the rhinoceros and tapir. The lower jaw is large, especially the region of the angle, which is expanded and flattened, giving great surface for the attachment of the masseter muscle. The condyle is greatly elevated above the alveolar border; its articular surface is very wide transversely, and narrow and convex from before backwards. The coronoid process is slender, straight, and inclined backwards. The horizontal ramus, long, straight, and compressed, gradually narrows towards the symphysis, where it expands laterally to form with the ankylosed opposite ramus the wide, semicircular, shallow alveolar border for the incisor teeth.
The vertebral column consists of seven cervical, eighteen dorsal, six lumbar, five sacral, and fifteen to eighteen caudal vertebrae.
There may be nineteen rib-bearing vertebrae, in which case five only will be reckoned as belonging to the lumbar series. The odontoid process of the axis is wide, flat, and hollowed above, as in the ruminants. The bodies of the cervical vertebrae are elongated, strongly keeled, and markedly opisthocoelous, or concave behind and convex in front. The neural laminae are broad, the spines almost obsolete, except in the seventh, and the transverse processes not largely developed. In the trunk vertebrae the opisthocoelous character of the centrum graduall y diminishes. The spinous processes of the anterior thoracic region are high and compressed. To these is attached the powerful elastic ligament (ligamentum nuchae, or " paxwax ") which, passing forwards in the middle line of the neck above the neural arches of the cervical vertebrae - to which it is also connected - is attached to the occiput and supports the weight of the head. The transverse processes of the lumbar vertebrae are long, flattened, and project horizontally outwards or slightly forward from the arch. The metapophyses are moderately developed, and there are no anapophyses. The caudal vertebrae, except those quite at the base, are slender and cylindrical, without processes and without chevron bones beneath. The ribs are eighteen or nineteen in number on each side, flattened, and united to the sternum by short, stout, tolerably well ossified sternal ribs. The sternum consists of six pieces; the anterior or presternum is compressed and projects forwards like the prow of a boat. The segments which follow gradually widen, and tie hinder part of the sternum is broad and flat.
As in all other ungulates, there are no clavicles. The scapula is long and slender, the supra-scapular border being rounded, and slowly and imperfectly ossified. The spine is very slightly developed; rather above the middle its edge is thickened and somewhat turned backwards, but it gradually subsides at the lower extremity without forming any acromial process. The coracoid is a prominent rounded nodule. The humerus is stout and rather short. The ulna is rudimentary, being represented by little more than the olecranon. The shaft gradually tapers below and is firmly welded to the radius. The latter bone is of nearly equal width throughout. The three bones of the first row of the carpus (scaphoid, lunar and cuneiform) are subequal in size. The second row consists of a broad and flat magnum, supporting the great third metacarpal, having to its radial side the trapezoid, and to its ulnar side the unciform, which are both small, and articulate inferiorally with the rudimentary second and fourth metacarpals. The pisiform is large and prominent, flattened and curved; it articulates partly with the cuneiform and partly with the lower end of the radius. The large metacarpal is called in veterinary anatomy " cannon bone"; the small lateral metacarpals, which gradually taper towards their lower extremities, and lie in close contact with the large one, are called " splint bones." The single digit consists of a moderate-sized proximal (os suffraginis, or large pastern), a short middle (os coronae, or small pastern), and a wide, semi-lunar, ungual phalanx (os pedis, or coffin bone). There is a pair of large nodular sesamoids behind the metacarpo-phalangeal articulation, and a single large transversely-extended sesamoid behind the joint between the second and third phalanx, called the " navicular bone." The carpal joint, corresponding to the wrist of man, is commonly called the " knee " of the horse, the joint between the metacarpal and the first phalanx the " fetlock," that between the first and second phalanges the " pastern," and that between the second and third phalanges the " coffin joint." In the hinder limb the femur is marked, as in other perissodactyles, by the presence of a " third trochanter," a flattened process, curving forwards and arising from the outer side of the bone, about one-third of the distance from the upper end. The fibula is reduced to a mere rod-like rudiment of the upper end. The lower part is absent or completely fused with the tibia. The calcaneum has a long and compressed calcaneal process. The astragalus has a large flat articular surface in front for the navicular, and a small one for the cuboid. The navicular and the external cuneiform bones are broad and flat. The cuboid is small, and the internal and middle cuneiform bones are small and united together. The metapodals and phalanges resemble very closely those of the fore limb, but the principal metatarsal is more laterally compressed at its upper end than is the corresponding metacarpal. The joint between the femur and tibia, corresponding to the knee of man, is called the " stifle-joint "; that between the tibia and tarsus, corresponding to the ankle of man, the " hock." The bones and joints of the foot have the same names as in the fore limb. The horse is eminently " digitigrade," standing on the extremity of the single digit of each foot, which is kept habitually in a position approaching to vertical.
The muscles of the limbs are modified from those of the ordinary mammalian type in accordance with the reduced condition of the bones and the simple requirements of flexion and extension of the joints, no such actions as pronation and supination, or opposition of digits, being possible or needed. The muscles therefore which perform these functions in other quadrupeds are absent or rudimentary.
Below the carpal and tarsal joints, the fore and hind limbs correspond almost exactly in structure as well as function. On the anterior or extensor surface of the limb a powerful tendon (7 in fig. 2), that of the anterior extensor of the phalanges (corresponding to the extensor communis digitorum of the arm and extensor longus digitorum of the foot of man) passes down over the metacarpal bone and phalanges, to be inserted mainly into the upper edge of the anterior surface of the last phalanx or pedal bone. There is also a much smaller second extensor on the outer side of this in each limb, the lateral extensor of the phalanges. In the fore-leg the tendon of this muscle (which corresponds with the extensor minimi digiti of man) receives a slip from that of the principal extensor, and is inserted into the first phalanx. In the hind-leg (where it is the homologue apparently of the peroneus brevis of man) the tendon becomes blended with that of the large extensor.
A strong ligamentous band behind the metapodium, arising from near the upper extremity of its posterior surface, divides into two at its lower end, and each division, being first connected with one of the paired upper sesamoid bones, passes by the side of the first phalanx to join the extensor tendon of the phalanges. This is called in veterinary anatomy the " suspensory ligament of the sesamoids," or of the " fetlock " (io in fig. 2); but its attachments and relations, as well as the occasional presence of muscular fibres in its substance, show that it is the homologue of the interosseous muscles of other mammals, modified in structure and function, to s ' '16 FIG. 2. - Section of Foot of Horse.
2, First phalanx (os suffraginis). 1, Metacarpal bone. I o, Suspensory ligament of fetlock.
3, Second phalanx (os coronae). Inferior or short sesamoid s, Third or ungual phalanx (os ligament.
pedis, or coffin bone). 12, Derma or skin of the foot, 5, One of the upper sesamoid covered with hair, and continued into bones.
6, Lower sesamoid or navicular 13, The coronary cushion, bone. 14, The podophyllous or laminar 7, Tendon of anterior extensor membrane, and of the phalanges. 15, The keratogenous membrane 8, Tendon of superficial flexor of the sole.
(fl. perforatus). 16, Plantar cushion.
17, Hoof.
9, Tendon of deep flexor (fl. perforans). 18, Fatty cushion of fetlock. suit the requirements of the horse's foot. Behind or superficial to this are placed the two strong tendons of the flexor muscles, the most superficial, or flexor perforatus (8) dividing to allow the other to pass through, and then inserted into the middle phalanx. The flexor perforans (9) is as usual inserted into the terminal phalange. In the fore-leg these muscles correspond with those similarly named in man. In the hind-leg, the perforated tendon is a continuation of that of the plantaris, passing pulley-wise over the tuberosity of the calcaneum. The perforating tendon is derived from the muscle corresponding with the long flexor of man, and the smaller tendon of the oblique flexor (tibialis porticus of man) is united with it.
The hoof of the horse corresponds to the nail or claw of other mammals, but is so constructed as to form a complete and solid case to the expanded termination of the toe, giving a firm basis of support formed of a non-sensitive substance, which is continually renewed by the addition of material from within, as its surface wears away by friction. The terminal phalange of the toe is greatly enlarged and modified in form to support this hoof, and the size of the internal framework of the foot is increased by a pair of lateral fibro-cartilaginous masses attached on each side to the hinder edges of the bone, and by a fibro-cellular and fatty plantar cushion in the median part. These structures are all enclosed in the middle subcorneous integument, a continuation of the ordinary skin of the limb, but extremely vascular, and having its superficial extent greatly increased by being developed into papillae or laminae. From this the horny material which constitutes the hoof is exuded. A thickened ring encircling the upper part, called coronary cushion (13) and the sole (15), are covered with numerous thickly-set 17 papillae or villi, and take the greatest share in the formation of the hoof; the intermediate part constituting the front and side of the foot (14), corresponding with the wall of the hoof, is covered with parallel, fine longitudinal laminae, which fit into corresponding depressions in the inner side of the horny hoof.
The horny hoof is divided into a wall or crust consisting of the front and sides, the flattened or concave sole, and the frog, a triangular median prominence, notched posteriorly, with the apex turned forwards, situated in the hinder part of the sole. It is formed of pavement epithelial cells, mainly grouped in a concentric manner around the vascular papillae of the subcorneous integument, so that a section near the base of the hoof, cut transversely to the long axis of these papillae, shows a number of small circular or oval orifices, with cells arranged concentrically round them. The nearer the surface of the hoof, or farther removed from the seat of growth, the more indistinct the structure becomes.
Small round or oval plates of horny epithelium called " chestnuts," callosities growing like the hoof from enlarged papillae of the skin, are found on the inner face of the fore-arm, above the carpal joint in all species of Equidae, and in the horse (E. caballus) similar structures occur near the upper extremity of the inner face of the metatarsus. They are evidently rudimentary structures which it is suggested may represent glands (Lydekker, Proc. Zool. Soc. London, 1903, vol. i.).
Dentition
The dentition of the horse, when all the teeth are in place, is expressed by the formula i. 3, c. i, p., m. 3 = 44. The incisors of each jaw are placed in close contact, forming a semicircle. The crowns are broad, somewhat awl-shaped, and of nearly equal size. They have all the great peculiarity, not found in the teeth of any other mammal, and only in the Equidae of comparatively recent geological periods (see also Palaeontology), of an involution of the external surface of the tooth (see fig. 3), by which what should properly be the apex is carried deeply into the interior of the crown, forming a pit, the bottom of which becomes partially filled with cement. As the tooth wears, the surface, besides the external enamel C"' :? °' layer as in an ordinary ?..,r simple tooth, shows in addition a second inner ring of the same hard substance surrounding the pit, which adds greatly to the efficiency of the tooth as an organ for biting tough, fibrous substances. This pit, generally filled in the living animal with particles of food, is FIG. 3 - Longitudinal and Transverse Section dark from its 3 - g dark colour, and con of Upper Incisor of Horse. stitutes the " mark " p, Pulp cavity. by which the age of d, Dentine or ivory. the horse is judged, e, Enamel. as in consequence of c, Outer layer of cementum or crusta petrosa. its only extending to c', Inner layer of cementum, lining a, the pit a certain depth in or cavity of the crown of the tooth. the crown it becomes obliterated as the latter wears away, and then the tooth assumes the character of that of an ordinary incisor, consisting only of a core of dentine, surrounded by the external enamel layer. It is not quite so deep in the lower as in the upper teeth. The canines are either rudimentary or absent in the female. In the male they are compressed, pointed, and smaller than the incisors, from which they are separated by a slight interval. The teeth of the cheek series are all in contact with each other, but separated from the canines by a considerable toothless space. The anterior premolars are quite rudimentary, sometimes not developed at all, and generally fall by the time the animal attains maturity, so that there are but six functional cheek teeth, - three that have predecessors in the milk-dentition, and hence are considered as premolars, and three molars, but otherwise, except the first and last of the series, not distinguishable in form or structure. These teeth in both upper and lower jaws are extremely long-crowned or hypsodont, successive portions being pushed out as the surface wears away, a process which continues until the animal becomes advanced in age. The enamelled surface is infolded in a complex manner (a modification of that found in other perissodactyles), the folds extending quite to the base of the crown, and the interstices being filled and the surface covered with a considerable mass of cement, which binds together and strengthens the whole tooth. As the teeth wear, the folded enamel, being harder than the other constituents, the dentine and cement, forms projecting ridges on the surface arranged in a definite pattern, which give it great efficiency as a grinding instrument (see fig. 2, in article Equidae). The free surfaces of the upper teeth are quadrate, except the first and last, which are nearly triangular. The lower teeth are much narrower than the upper.
The milk-dentition consists of i. g, c. a, m. g =24, - the canines and first or rudimentary premolars having apparently no predecessors. In form and structure the milk-teeth much resemble the permanent ones, having the same characteristic enamel-foldings. Their eruption commences a few days after birth, and is complete before the end of the first year, the upper teeth usually appearing somewhat earlier than the lower. The first teeth which appear are the first and second milk-molars (about five days), then the central incisor (from seven to ten days); this is followed by the second incisor (at one month), then the third molar, and finally the third incisor. Of the permanent teeth the first molar appears a little after the end of the first year, followed by the second molar before the end of the second year. At about two and a half years the first premolar replaces its predecessor. Between two and a half and three years the first incisor appears. At three years the second and third premolars, and the third molar have appeared, at from three and a half to four years the second incisor, at four to four and a half years the canine, and, finally, at five years, the third incisor, completing the permanent dentition. Up to this period the age of the horse is clearly shown by the condition of dentition, and for some time longer indications can be obtained from the wear of the incisors, though this depends to a certain extent upon the hardness of the food or other circumstances. As a general rule, the depression caused by the infolding of the surface of the incisor (the " mark ") is obliterated in the first or central incisor at six years, in the second at seven years, and in the third at eight years. In the upper teeth, as the depressions are deeper, this obliteration does not take place until about two years later. After this period no certain indications can be obtained of the age of the horse from the teeth.
Digestive Organs
The lips are flexible and prehensile; and the membrane that lines them and the cheeks smooth. The palate is long and narrow; its mucous surface has seventeen pairs of not very sharply defined oblique ridges, extending as far back as the last molar tooth, beyond which the velum palati extends for about 3 in., having a soft corrugated surface, and ending posteriorly in an arched border without a uvula. This embraces the base of the epiglottis, and, except while swallowing food, shuts off all communication between the cavity of the mouth and the pharynx, respiration being, under ordinary circumstances, exclusively through the nostrils. Between the mucous membrane and the bone of the hard palate is a dense vascular and nervous plexus. The membrane lining the jaws is soft and corrugated. An elongated raised glandular mass, 3 in. long and 1 in. from above downwards, extending backwards from the root of the tongue along the side of the jaws, with openings on the surface leading into crypts with glandular walls, represents the tonsil. The tongue, corresponding to the form of the mouth, is long and narrow. It consists of a compressed intermolar portion with a flat upper surface, broad behind and becoming narrower in front, and of a depressed anterior part rather shorter than the former, which is narrow behind and widens towards the evenly rounded apex. The dorsal surface generally is soft and smooth. There are two large circumvallate papillae near the base, rather irregular in form, about a quarter of an inch in diameter and half an inch apart. The conical papillae are small and close set, though longer and more filamentous on the intermolar portion. There are no fungiform papillae on the dorsum, but a few inconspicuous ones scattered along the sides of the organ.
Of the salivary glands the parotid is by far the largest, elongated in the vertical direction, and narrower in the middle than at either end. Its upper extremity embraces the lower surface of the cartilaginous ear-conch; its lower end reaches the level of the inferior margin of the mandible, along the posterior margin of which it is placed. Its duct leaves the inferior anterior angle, at first descends a little, and runs forward under cover of the rounded inferior border of the lower jaw, then curves up along the anterior margin of the masseter muscle, becoming superficial, pierces the buccinator, and enters the mouth by a simple aperture opposite the middle of the crown of the third premolar tooth. It is not quite so thick as a goosequill when distended, and nearly a foot in length.
