Fig. 93.—Tilapia dolloi. To show the external characters of an Acanthopterygian Teleost. A, side view; B, the first branchial arch. a.f, Spinose part of the anal fin; a.f1, soft rays; c.f, caudal fin; d.f, spinose portion of the dorsal fin; d.f1, soft rays; g.f, gill filaments; g.r, gill rakers; i.l.l, inferior lateral line; n, nostril; p.f, pelvic fin; p.op, preoperculum; pt.f, pectoral fin; s.l.l, superior lateral line; t.s, transverse row of scales. (From Boulenger.)
In Fishes the characteristic shape of the body is more or less that of a spindle, tapering at each end and somewhat flattened from side to side; and, as a rule, the three regions of the body—head, trunk, and tail—pass almost imperceptibly into one another (Fig. 93, A). Nevertheless, there is great diversity of form in different Fishes. Compare, for example, the elongated, cylindrical shape of the Eels (which is perhaps associated with their habit of insinuating themselves into holes and crevices, and their undulatory, snake-like movements when swimming); the compressed, band-like shape of the Ribbon-Fishes (Trachypteridae); the flattened bodies of those Fishes which habitually live and move on the bottom, like the Skates and Rays; the thin, laterally-compressed bodies, often nearly as high as long, of the Flat-Fishes (Pleuronectidae), which always swim and rest on either the right or left side; the almost spherical Globe-Fishes (Tetrodon) which often float passively in the water; and the singular rectangular, coffin-like Coffer-Fishes (Ostracion). There is also much difference in the relative proportions of the three regions of the body in different Fishes, as witness the enormous size and grotesque appearance of the head of the Angler-Fish (Lophius); the huge high trunk and abbreviated tail of the Sun-Fish (Orthagoriscus); and the short high trunk and long tail of Notopterus (Fig. 334).
In its external appearance the head perhaps differs more in different Fishes than any other part of the body. Long and flattened in the Skates and Rays, the head becomes short and high in most Holocephali and in many Teleosts, or is shaped like a blunt cone, as in such Dipnoi as Protopterus and Lepidosiren; or becomes long and pointed, as in the North American "Gar Pike" (Lepidosteus); or, finally, as in the Hammer-head Shark (Sphyrna), the head may be produced into great lateral extensions, carrying the eyes at their extremities (Fig. 256, B). Apart from its relative shape and size, the appearance of the head may be further modified by the thinness of the investing scaleless skin, which readily allows the surface and contour lines of the bones of the skull to be seen through it, as in the Crossopterygii, and in such Teleosts as the Siluroid genera Clarias and Callichthys; or the skin, even if devoid of scales, may be so thick that scarcely any of the bones are visible externally. The exoskeleton, whether in the form of scales or bony plates, may extend to a varying degree on to the surface of the head in different Teleosts, or may even invest nearly the whole of the head. When, as is not infrequently the case (e.g. many Scorpaenidae) certain of the bones of the skull are produced into projecting spines, the head assumes a singularly formidable appearance (Fig. 424).
The mouth differs greatly in size and position. In existing Elasmobranchs it is generally crescentic in shape and always ventral in position, but in certain primitive fossil members of the group, as in the Palaeozoic Cladoselache, it is anterior and terminal. The Sturgeon and other living Chondrostei have the mouth ventral. In the Dipnoi also the mouth is ventral, but is near the extremity of the snout. As a rule, the mouth is terminal or nearly so in the living Crossopterygii and Holostei, and in the great majority of Teleosts, although in the latter group it is occasionally distinctly ventral, especially when a snout is developed, and it may sometimes look upwards by reason of the projection of the lower jaw in front of the upper. A pronounced "beak" is sometimes formed by the forward prolongation of both jaws, as in the Gar Pike (Lepidosteus), with the result that the vertical gape of the mouth is greatly increased, but in a few Teleosts a beak may result from a forward extension of one jaw only, the upper in the Sword-Fish (Xiphias) and the lower in the "Half-Beak" (Hemirhamphus). A further modification is to be noted in many Teleosts, in which, owing to the forward prolongation and inclination of the skeletal supports of the jaws, the mouth is at the extremity of a longer or shorter spout-like beak, and is then usually very small. This is the case in the "Sea-Horse" (Hippocampus), the Pipe-Fishes (Syngnathus), the "Flute-mouths" (Fistularia), and the Trumpet-Fish (Centriscus), and especially in certain species of the African family Mormyridae, where the pore-like mouth is at the extremity of a long, tapering, downwardly-curved proboscis (Fig. 330). In many Teleosts the mouth can be protruded and withdrawn at will by a sliding motion of the bones of the upper jaw (premaxillae) on the anterior skull bones by which they are supported. From this point of view the toothless mouth of the Sturgeon is even more remarkable. By a forward or a backward swing of the elements which form the upper half of the hyoid arch (hyomandibular and symplectic) the mouth can be thrust downwards from the under side of the head like a spout, when the Fish is feeding, and subsequently retracted. In not a few Fishes the forepart of the head is prolonged forwards over the mouth and jaws in the form of a rostrum or "snout"; it is, in fact, to the growth of a snout that the ventral position of the mouth in Fishes is generally due. This feature is more or less characteristic of most Elasmobranchs, in which the snout forms a cut-water overhanging the mouth. In the Holocephali the snout is short and blunt, except in Harriotta, where it is pointed and unusually long. Among the Chondrostei the Sturgeon has an exceptionally massive snout, the length and shape of which differs in different species. In the allied Polyodon the thin, flattened, spoon-like snout is scarcely less than one-fourth the length of the body (Fig. 289).
Simple or branched tactile filaments or "barbels" are present on different parts of the head in many Teleostomi, sometimes at or near the chin, as in certain Gadidae, like the Haddock and Cod, or on the under surface of the snout, in front of the mouth, as in the Sturgeon. In the Siluridae (Fig. 356), where they are found in relation with the upper and lower jaws, and even between the nostrils, these structures are often remarkably developed.
The eyes of Fishes are usually very large. They are generally situated on the sides of the head, but in the "Star-gazers" (Uranoscopus) they are on the upper surface and close together. In the goggle-eyed Periophthalmus the eyes seem to protrude from their orbits, and in a variety of a species of Carp, the Gold-Fish (Cyprinus auratus), the protrusion is so marked that the eyes seem as if on stalks. In a few species, which live either in caves or at very great oceanic depths, the eyes become vestigial, and are hidden beneath the skin, or are even covered by scales (Fig. 430).
In the Elasmobranchs and Dipnoi the olfactory organs retain their primitive position as pit-like sacs on the ventral surface of the snout, just in front of the mouth. In the Dipnoi (e.g. Protopterus) each olfactory sac has two apertures, of which one, the external nostril, is placed on the under surface of the snout, while the other, the internal nostril, opens within the upper lip into the oral cavity—a feature which is unique among Fishes. In nearly all Teleostomi, also, each sac has two nostrils, which, however, are situated either on the upper surface or on the sides of the fore-part of the head, and have no communication with the mouth.
Directly behind the head in Elasmobranchs, or beneath its hinder part in all other Fishes, are placed the external apertures of the branchial clefts. In the former group these apertures are visible externally in the form of a series of narrow vertical slits, but in the latter they communicate with the exterior by opening on each side into a common branchial cavity, the outer wall of which is formed by a movable flap-like fold with a free hinder margin and a special internal skeleton of cartilaginous rays or of bony plates and rods, the gill-cover or operculum (Fig. 161, B). Behind the free margin of the operculum there is a slit-like orifice, the gill-opening or external branchial aperture, which curves from above downward and forward toward the chin, and places the branchial cavity in communication with the exterior. Through this aperture the water, which has entered through the mouth, traversed the gill-clefts, and bathed the gills, finds its exit from the body. The space on the ventral side of the head between the two halves of the lower jaw, and between the two external branchial apertures, is termed the "isthmus." The size of the external branchial aperture differs greatly in different Fishes, according to the extent to which the free opercular margin fuses below with the isthmus, or behind with the side of the head. Thus the aperture may extend from the chin in front upward and backward to near the dorsal surface of the head, or it may be reduced to little more than a mere pore situated on any part of the opercular edge (e.g. Hippocampus); or, as in Symbranchus, the reduced pores of opposite sides may coalesce in the floor of the throat in a common median opening.
In the Elasmobranchs and in the Dipnoi the cloacal aperture is always situated at the junction of the trunk with the tail. In the Teleostomi, however, where the intestine has a separate external orifice or anus, distinct from, and placed in front of, the separate or combined urino-genital ducts, the anus may either retain its primitive position near the union of the trunk and tail, or occupy almost any intermediate position between this point and the throat.