The Cambridge Natural History

The Central Nervous System is dorsal and tubular as in Vertebrates, and lies in a connective-tissue sheath immediately above the notochord (Figs. 71, etc., and 80, A). Posteriorly it tapers to a fine point a little in front of the end of the notochord, but anteriorly it ends abruptly some distance behind the anterior extremity of the notochord. The central canal is connected with the dorsal surface by a median longitudinal cleft (Fig. 80, C), and at the anterior end it dilates to form the cerebral vesicle (c.v) with which two simple sense-organs, an eye-spot (e) and an olfactory pit (olf), are connected. A patch of ciliated epithelium in the floor of the vesicle has been described as an "infundibular-organ." There is also a surface dilatation of the dorsal cleft behind the cerebral vesicle (dil). The nervous system as far back as this point may be regarded as the brain, though scarcely distinguishable externally (Figs. 71 and 80, A) from the spinal chord behind. From this "brain" arise two pairs of "cranial" nerves, the first (I.) from the anterior end, and the second (II.) from the dorsal surface of the cerebral vesicle; both are in front of the first myotomes of the body, and supply the pre-oral snout with nerves.

The spinal cord gives off a large number of spinal nerves segmentally arranged, but, like the myotomes, not opposite and symmetrical on the two sides, but placed alternately (Fig. 81). Moreover, the spinal nerves arise on each side at two levels, there being a more dorsal series each arising by a single root and supplying the integument as well as the transverse muscles, so as to be sensory as well as motor, and a ventral series arising each by a number of roots (Fig. 81) and wholly motor in function, as they supply only the myotomes. These two series may be compared to the dorsal and ventral roots which in the Vertebrata join to form a mixed spinal nerve.

In addition to ordinary small nerve cells the central nervous system contains certain large nerve cells with very long processes, the "giant fibres," which extend through the greater part of the length of the spinal cord. No trace of a sympathetic nervous system has been found.

The Sense-Organs connected with the nervous system are few and simple. There are sensory cells in the ectoderm, on the margin of the velum, on the velar tentacles, and especially in clumps on papillae of the cirri around the mouth, which are probably tactile. In the roof of the oral hood there is a sensory structure, the "groove of Hatschek," which is supposed to be an organ of taste. The olfactory pit alluded to above opens externally on the left-hand side of the snout. It is ciliated internally and leads to the so-called olfactory lobe, an antero-dorsal hollow outgrowth from the brain. In the young animal the olfactory pit opens by the neuropore into the central canal (Fig. 80, A), but that passage is closed in the adult. Possibly the olfactory pit is homologous with the hypophysis or pituitary body of Vertebrates, the homologue of which in Tunicata has a ciliated funnel. Finally, the median cerebral eye (Figs. 80 and 81) is a mere pigment spot in the anterior wall of the cerebral vesicle, and a series of somewhat similar pigment spots occurs along the floor of the central canal in the spinal cord.^[114] There is no known auditory organ. On the under surface of the oral hood patches of ciliated epithelium drawn out into rounded lobes were called by Johannes Müller the "Räder-organ." This is probably of use in drawing water inwards to the pharynx, but it may also be a sense-organ.

The Gonads are segmentally arranged along the sides of the body, projecting into the atrial cavity at the sides of the pharynx and intestine. In some species the gonads are paired, but in others belonging to the genus Asymmetron (p. 137) only a single series, that of the right side, is present. In the common Amphioxus (Branchiostoma lanceolatum) there are about 26 pairs (Fig. 70, B), lying in somites 25 to 51; and ovaries and testes are found in separate individuals in all other respects. Each gonad is surrounded by a layer of coelomic epithelium. The gonad must therefore be regarded as having grown down from a myotome of the body-wall into a coelomic pouch, carrying before it the coelomic and then the atrial epithelium (Figs. 72, and 74, A, g). Eventually the gonads, when ripe, burst through the layers of epithelium, and the ova and sperms are shed into the atrium and escape to the exterior by the atriopore, or it may be in some cases by the mouth.

Development takes place in the sea-water where the egg is fertilised—apparently always about sunset, the embryonic stages being passed through during the night, and the larva hatched in the early morning.

The egg is small (0.105 mm. in diameter when shed) and contains very little food-yolk. Segmentation is complete (Fig. 82, A), is nearly regular, and results in the formation of a hollow blastosphere (Fig. 82, E, F), the wall of which is one cell thick. The lower cells (Fig. 82, B, C, D) are slightly larger than the upper. Invagination of the lower cells then takes place (Fig. 83, A), resulting in the suppression of the blastocoele or segmentation cavity and the formation of an archenteron, at first shallow and opening widely to the exterior (Fig. 83, B), and then deeper and with the opening narrowed to a small posterior blastopore (Fig. 83, C). This "gastrula" stage differs from the blastosphere in having a mouth or blastopore, and in being two cell-layers thick—epiblast (ectoderm) on the outside and hypoblast (endoderm) within. It soon shows the future aspects of the body by its elongation and shape (Fig. 83, C), as the dorsal surface becomes flat and the ventral convex, while the blastopore is at the posterior end of the dorsal surface. The blastopore soon closes, and the mouth and anus are formed independently later.

The epiblast cells become ciliated all over the surface, so that the embryo rotates within the thin covering which still surrounds it. And now all the chief systems of the body begin to be marked out. The tubular nervous system develops from a depression of the epiblast (the medullary plate) in the middle line of the flattened dorsal surface (Fig. 84, A, mp). The edges of the depressed area grow inwards and unite over the deeper layer of epiblast, which becomes the wall of the neural canal or embryonic nervous system (Fig. 84, D, n); and further back these edges of the medullary plate join one another behind the blastopore, so that the latter comes to open into the floor of the neural canal, thus forming the neurenteric canal (Fig. 85, A, cn). Anteriorly the neural canal (n) opens to the exterior for some time by the neuropore.

The hypoblastic walls of the archenteron give off a long median dorsal groove which becomes the notochord (Fig. 84, C and D, ch); and also an anterior pouch and certain lateral pairs of diverticula which are the enterocoeles or coelomic pouches, and give rise to the mesoblastic somites (Fig. 84, B and C, mk). The notochord (Fig. 84, D, ch) is at first a longitudinal cellular ridge, which becomes segmented off from the hypoblast as a rod lying below the neural canal. It is seen in various stages of development in Figs. 84 and 86, leading to the vacuolated condition of the adult.

The coelomic pouches are five in number—(1) one median, anterior, which gives rise to the two head cavities, the left-hand one of which opens to the exterior by means of the pre-oral pit; (2) a pair of small lateral pouches, placed anteriorly and dorsally, which do not divide but give rise to the first pair of myotomes only and their outgrowths which extend back into the metapleural folds, where, however, they are later replaced by lymph spaces; and (3) a second pair of diverticula, more posteriorly placed, which continue to grow back towards the blastopore, and have paired mesoblastic somites, the cavities in which are the beginnings of the coelom in the body, constricted off from them successively from before backwards (Fig. 85, A, ush) to form all the remaining myotomes.^[115] This is the first sign of segmentation in the animal, and at this stage, when it has about five pairs of mesoblastic somites, it breaks out of its covering and becomes a free-swimming larva.

The mouth now appears, and soon grows to a large opening on the left side of the now pointed anterior end (Fig. 86, A, m), and the first gill-slit (ks) forms as a direct communication from the front of the mesenteron (pharynx) to the exterior. It is ventral at first, and then shifts over to the right side.

The anus forms posteriorly, and the neurenteric canal closes up. A depression on the floor of the enteron close to the mouth gives rise to the "club-shaped gland" (Fig. 86, B, k), which is probably a gill-cleft in its nature.

The walls of the coelomic pouches, which have been extending both dorsally and ventrally (Fig. 84, D), become the mesoderm, the outer the somatic and the inner the splanchnic layer; and the ventral parts of their cavities unite to form the coelom. The cells of the dorsal parts become muscle fibres, and constitute the myotomes internally and the connective tissue of the skin externally.

The larva (Fig. 87) is now long and narrow with many segments, pointed ends, and a caudal fin. The gill-slits all appear first in the mid-ventral line and then shift over to the right side (Fig. 87, 1-4): they are metamerically arranged. After fourteen have been so formed a series of eight appear dorsally to those on the right side, and then the first set, originally ventral, move over to the left side, and by the suppression of some they become equal in number and segmentally arranged on the two sides of the body. This is perhaps the stage at which Amphioxus shows the nearest approach to the typical embryo of a higher Vertebrate. The gill-slits are here seven to nine on each side, and the Vertebrate embryo has usually five to seven on each side. These first gill-slits in Amphioxus are later subdivided by the downgrowth of the tongue-bar from the dorsal edge.

The atrium is an ingrowth of the external space between the two ventral metapleural or atrial folds (Figs. 88 and 89), paired lateral ridges of the body-wall, and so is lined by ectoderm. This ingrowth is shut off from the exterior by the growth towards each other of sub-atrial ridges on the inner sides of the metapleural folds (see Fig. 89, A, sl), and then becomes greatly enlarged by the increased relative growth of the ventro-lateral part of the body-wall (Fig. 89, B, C). The posterior opening between the metapleural folds remains as the atriopore (Fig. 88, C, ap); while the anterior end (Fig. 88) also remains open for some time, but eventually closes. As the metapleural folds lie outside the gill-slits (Fig. 88, A) when these folds close in (B and C), it comes about that the gill-slits which formerly opened freely to the exterior now open into the cavity of the atrium (compare Figs. 87 and 88).

The mouth now becomes median and ventral, and is reduced in size, the oral hood (stomodaeum) is formed in front of it, the gill-slits become more numerous and vertically elongated, the endostyle forms along the floor of the pharynx, and the gonads grow as paired pouches from the body-wall. This brings the animal to the young adult condition, reached at a period of probably about three months after the fertilisation of the egg.

The development as a whole shows a very marked resemblance to that of the Tunicata (see p. 55), but lends no support to the view that Amphioxus has degenerated from a higher group of the Vertebrata.

Thus sixteen species have been described, of which the three under Branchiostoma placed after square brackets, seem to be merely varieties of B. lanceolatum, and B. nakagawae is probably identical with B. belcheri; while it is a question whether Asymmetron caudatum is more than a variety of A. lucayanum, thus leaving eleven or twelve species that seem fairly well characterised. The exact positions of the two marked (?), viz. B. elongatum and B. pelagicum, cannot be determined in the absence of fuller descriptions of these species.

The list above, and the map (Fig. 90), give some indication of the geographical distribution of the group, and show that, although the few species are widely distributed over the shallow waters of the globe, most of the records lie between 40° N. and 40° S. latitudes. In fact the group is mainly a tropical one, and is most abundant in the Indo-Pacific region. The crosses indicate records of species of Branchiostoma, and the circles those of Asymmetron (including Heteropleuron); the latter are confined to the Indo-Pacific seas, with the exception of A. lucayanum from the Bahamas—one of the numerous cases of interesting similarity between the marine faunas of the East and West Indies.

FISHES
(EXCLUSIVE OF THE SYSTEMATIC ACCOUNT OF TELEOSTEI)

T. W. BRIDGE, Sc.D., F.R.S.

Trinity College, Cambridge; Mason Professor of Zoology and Comparative
Anatomy in the University of Birmingham

CHAPTER V

THE SYSTEMATIC POSITION AND CLASSIFICATION OF FISHES

In the first chapter of this volume it was pointed out that the Craniata, of which the Fishes form a subordinate group, is the last of the four principal divisions into which the Chordata are divided. The animals included in the first three, viz. the Hemichordata, the Urochordata, and the Cephalochordata, have already been dealt with in the earlier chapters, and it now remains for us briefly to consider the diagnostic characters of the Craniata, and then, more in detail, the organisation of the Fishes.

The Craniata, often termed Vertebrata, form one of the best defined and most easily recognisable divisions of the animal kingdom. As the name implies, they are distinguished from the more primitive Chordata by the formation of a definite "head," as the result of the modification of the anterior portion of the central nervous system to form a complex brain, round which are concentrated the chief organs of special sense. This is combined with the evolution of a skull, which, in addition to providing a "cranium" for the enclosure and protection of the brain, and partial or complete capsules for the sense-organs, is connected behind with a system of bony or cartilaginous visceral arches, which loop round the pharynx between the gill-clefts. Besides supporting the breathing organs (gills) in the lower aquatic Craniata, or existing as embryonic vestiges in the higher lung-breathing forms, these arches usually form the basis of jaws for the mouth. The epidermal portion of the superficial skin is always composed of several layers of cells. The notochord, which is always present in the embryo, and in a few Craniates, both living and extinct, may even be retained in its entirety in the adult, fails to reach the anterior end of the brain. In most Craniates, however, the notochord becomes more or less completely replaced in the adult by the development round it of a series of vertebrae, forming the backbone or vertebral column. Two pairs of limbs, and cartilaginous or bony limb-girdles for their support, are very generally present.

The segmentation, or serial repetition of certain organs of the body, which is so marked a feature in the Cephalochordata, is also characteristic of the Craniata. Examples of this may be seen in the division of the lateral longitudinal muscles of the body wall into muscle-segments or myotomes by a series of transverse fibrous septa; in the formation of the vertebral column by a series of successive joints or vertebrae; in a similar serial repetition of the cranial and spinal nerves, the gill-clefts and branchial arches, certain blood-vessels, and the renal tubules. There is sometimes, however, no precise regional or numerical correspondence between the different organs which are successively repeated in this way, and hence it is probable that, in at least some of the organs of the Craniate body, the segmentation has been independently evolved in each case.

The pharynx is relatively much shorter than in other Chordata. The gill-clefts are few in number, whether, as in the lower Craniata, they are retained as the functional breathing organs, or are present, as vestiges only, in the embryos of the higher members of the group. In no instance are they subdivided by the growth of "tongue-bars" or "synapticula," nor do they open externally into an atrial or peribranchial cavity. The liver is a massive compound tubular gland, never, in the adult at all events, a simple caecal sac; and usually there is a pancreas and a spleen.

A spacious epithelium-lined body cavity or coelom, which, as regards its origin, may be regarded as a "syncoelom,"^[117] surrounds the alimentary canal and separates it from the body wall. From the epithelial walls of the coelom are derived the gonads (ovaries and testes), which in the adult are limited to a single pair; while paired and often segmentally-arranged lateral tubular outgrowths from it (renal tubuli) acquire a glandular character and form the basis of the excretory or kidney system. A special portion of the coelom also surrounds the heart and forms a pericardial cavity, and in some Craniata the genital ducts may be formed from its lining membrane.

There is always a muscular heart, consisting of at least three chambers, a sinus venosus, an auricle and a ventricle, and formed by a modification of the initial portion of the ventral or cardiac aorta of the Cephalochordata. The disposition of the great blood-vessels is based on a common plan in all Craniata, and the blood which circulates in them is red in colour owing to the presence of red, haemoglobin-containing corpuscles in addition to the colourless leucocytes which alone are present in the Cephalochordata. Ductless blood-glands of various kinds (spleen, thyroid, thymus, inter- and ad-renal bodies) are very generally present, and modify in different ways the character of the blood as it circulates through them. Besides blood-vessels there is also a somewhat similar system of lymphatic vessels distributed throughout the organs and tissues of the body, which serves the purpose of re-collecting the fluid portion of the blood that has diffused from the blood-vessels for the nutrition of the tissues, and conveying it back to the blood vascular system. These lymphatics contain lymph, a fluid comparable to dilute blood plasma, in which leucocytes float. In addition to their continuity with the blood-vessels at certain points, the lymphatic vessels may also communicate with the coelom, and hence the Craniata must be included among those somewhat rare exceptions to the general rule that no connexion exists between the series of blood-containing channels and the coelom.

In the excretory system the renal tubuli in the adult Craniata rarely retain their primitive embryonic communication with the coelom, and in no instance have they separate and independent external apertures; on the contrary, by the union of their outer or distal extremities, common efferent ducts are formed, which either open into a "cloaca," or directly on to the exterior of the body near the anus.

In all Craniates the dorsally-placed and tubular central nervous system has its anterior portion enlarged and otherwise modified to form a "brain," while the remaining portion, retaining a simpler and more uniform structure, forms the spinal cord. In the embryo the brain always consists of three successive sac-like enlargements known as the fore-, mid-, and hind-brain, and from these are developed the various parts of the complex adult brain, which in the disposition and mutual relations of its parts conforms to a common plan in all the members of the group. There are at least ten pairs of cranial nerves having their origin from the brain, and, in addition, a varying number of spinal nerves arising from the spinal cord, and as a rule formed in each case by the union of a mainly sensory, ganglionated, dorsal root with a mainly motor, non-ganglionated, ventral root.

The median and usually vestigial, parietal, or pineal eye may sometimes be retained as a functional organ, but there exist in all Craniates, in addition, paired eyes, the sensory portion of which, the retina, is derived as an outgrowth from the first of the primary embryonic brain-vesicles. To these organs of special sense are added a pair of auditory organs, and a pair of olfactory organs, besides, in the lower aquatic Craniates, the peculiar sensory organs of the "lateral line."

The gonads are reduced to a single pair in the adult, although it is possible that they may have a multiple origin in the embryo. Gonoducts for the discharge of the sex-cells are almost invariably present, and may owe their origin either to a change of function on the part of certain kidney-ducts, or to independent evolution from the lining membrane of the coelom. The ova are generally provided with a large amount of nutritive reserve in the shape of food-yolk, and hence the process of segmentation is frequently partial or "meroblastic," but in some groups, in which the ova have less food-yolk, it is complete or "holoblastic." The typical invaginate gastrula stage, which is so striking a feature in the embryonic history of the lower Chordata, occurs also in a few of the lower Craniates, but in most of them it is apt to become masked or modified in various ways by the presence of a superabundant amount of food-yolk.

Functional hermaphroditism is of very rare occurrence in Craniates, and, as in the Cephalochordata, reproduction by budding and the formation of colonies are unknown.

Thus distinguished from other Chordata, the Craniata are divided into six "classes," which may be variously grouped, as the following table shows:—

Ichthyopsida. Breathing by gills at some period of life. Anamniota No embryonic covering or amnion. Anallantoidea. No embryonic respiratory organ or allantois.			brace	I. Cyclostomata. Lampreys and Hag-Fishes.	brace	Agnathostomata. Without biting jaws.
				II. Pisces. True Fishes.	brace	Gnathostomata. With biting jaws.
				III. Amphibia. Newts, Frogs, and Toads.
Amniota. Amnion present. Allantoidea. Allantois present	brace	Sauropsida.	brace	IV. Reptilia. Lizards, Snakes, Turtles, and Crocodiles.
				V. Aves. Birds.
				VI. Mammalia. Hairy Quadrupeds.

Ichthyopsida. Breathing by gills at some period of life. Anamniota No embryonic covering or amnion. Anallantoidea. No embryonic respiratory organ or allantois.		I. Cyclostomata. Lampreys and Hag-Fishes.	Agnathostomata. Without biting jaws.
		II. Pisces. True Fishes.	Gnathostomata. With biting jaws.
		III. Amphibia. Newts, Frogs, and Toads.
Amniota. Amnion present. Allantoidea. Allantois present	Sauropsida.	IV. Reptilia. Lizards, Snakes, Turtles, and Crocodiles.
		V. Aves. Birds.
		VI. Mammalia. Hairy Quadrupeds.

Apart from the distinctive characters of the six "classes" into which the Craniata are divided, two or three of these classes may possess important structural features in common by which they are distinguished from others. Thus, Cyclostomata, Fishes and Amphibia agree with one another, and differ from all the remaining groups in breathing by gills and in possessing lateral line sensory organs during part, or the whole, of life. Their embryos have no investing amnion, neither does the sac-like outgrowth from the hind-gut, which is known as the allantois, if present at all, ever extend beyond the coelom to form an embryonic investment or to act as a primitive breathing organ. Hence, therefore, the terms Ichthyopsida, Anamniota, and Anallantoidea have been applied to these three classes. Similarly, the term Sauropsida, as applied to Reptiles and Birds, is a convenient means of giving expression to the fact that, underlying the most striking diversity of outward form and habits, there is a community of inward structure which justifies the conclusion that these animals are more closely related to one another than either group is to any other class of Craniates. And again, the application of the terms Agnathostomata and Gnathostomata brings into sharp relief the fundamental distinction between the Cyclostomata and all the remaining groups of Craniata which is only partially illustrated by the presence or absence of biting jaws.

In a general and popular sense the Cyclostomata are usually regarded as "Fishes," but this usage rests on no better foundation than a certain agreement between the Cyclostomata and the true Fishes in outward form and habits, and in their method of respiration by gills. On the other hand, it has been maintained that the distinctive features of the Cyclostomata are of sufficient importance not merely to separate them from the true Fishes, but possibly even (as is to some extent expressed by the use of the terms Agnathostomata and Gnathostomata) to warrant their elevation to a group equal in taxonomic value to all the remaining living Craniata taken collectively. The organisms included in the Cyclostomata, the Lampreys, and especially the Hag-Fishes, exhibit in many respects an extremely low grade of Craniate structure; but how far the simplicity or archaic nature of some of their organs is primitive, or has been acquired through degeneration, it is difficult, and is sometimes impossible, to determine with any degree of satisfaction. In other respects, such as the presence of a rasping "tongue," it is obvious that the Cyclostomata have attained a high degree of specialisation. As one of several illustrations which might be given of difficulties of this kind, it may be mentioned that it is by no means certain that the Cyclostomata are not the degenerate descendants of primitive but now extinct Gnathostomata. At all events the presence of paired cartilages in the skull of the Lamprey, which, with some show of reason, may be regarded as representatives of the primitive upper and lower jaws of the latter group, would seem to suggest this conclusion. If this be correct, we must regard the formation of a suctorial buccal funnel, with its complex system of supporting cartilages—one of the most striking features in the structure of this animal—as a secondary and adaptive specialisation of a mouth originally provided with biting jaws. But in spite of such difficulties there can be no question that the Cyclostomata are the most primitive of all existing Craniates, and so far differ from the true Fishes and from all other classes of Craniate animals, that their inclusion in a class by themselves is the least that can be done to give graphic expression to their isolated position, even if we do not fully accept the dictum of Haeckel that "they are further removed from Fishes than Fishes from Man."

Briefly stated, the Cyclostomata or Agnathostomata are distinguished from "Fishes" and all the remaining Craniata (Gnathostomata) by the following characters:—

The mouth is either nearly terminal, as in the Hag-Fishes (Myxine); or, as in the Lampreys (Petromyzon), it opens out of a spacious, pre-oral, suctorial, buccal funnel, which, in its relations to the hypophysis or pituitary body, recalls the pre-oral buccal cavity of the Cephalochordata. As in Amphioxus, the hypophysis^[118] is displaced dorsally by the forward growth of the pre-oral portion of the head in the embryo, and consequently it only attains its normal relations to the infundibular downgrowth^[119] from the ventral surface of the fore-brain by perforating the floor of the skull from above instead of from below as in all other Craniates. In one section of the group (e.g. Myxine) the hypophysis opens into the oral cavity, and serves as a tubular passage for the inspiratory water-current to the gill-sacs, a feature in which these Cyclostomes are unique. The apparently median olfactory organ is carried inwards with the hypophysial involution, and communicates with the latter throughout life. A primitive upper jaw (palato-quadrate cartilages or sub-ocular arches) is present, and in at least some Cyclostomes (e.g. the Lampreys), and possibly in all, there are structures which very probably represent a primitive lower jaw (Meckel's cartilages); but such structures are always non-biting, and merely form skeletal supports for other portions of the skull. In place of biting jaws the mouth is provided with a complex rasping lingual apparatus supported by special cartilages, the so-called tongue, which bears horny teeth and is capable of protrusion and retraction. Paired limbs are entirely wanting.

In the Gnathostomata, on the contrary, there is no buccal funnel, and the mouth, whether terminal or ventral in position, opens directly outwards. The hypophysis is usually carried inwards with the stomatodaeal invagination which in the embryo gives rise to the mouth, and is therefore from the first in relation with the ventral surface of the brain. Biting jaws (palato-quadrate and Meckelian cartilages), formed by the modification of an anterior and primitively gill-bearing visceral arch, are invariably present. The olfactory organs are obviously paired, and they are distinct from the hypophysis. Paired limbs are present.

As previously stated, the true Fishes form the second of the six "classes" into which the Craniata are divided. As compared with the higher Craniata, their distinctive characters may be concisely stated as follows:—

Fresh water or marine Gnathostomata, which in their shape and in method of breathing are adapted for an aquatic life. Throughout life their respiratory organs are in the form of vascular processes (gills) derived from the walls of the branchial clefts, and supported by a series of branchial arches. The principal organ of locomotion is the powerful muscular tail; in addition, however, there are paired fins, pectoral and pelvic, corresponding to the fore- and hind-limbs of the terrestrial Craniata, and possessing a supporting cartilaginous or bony skeleton ("ichthyopterygium") which cannot readily be compared with the limb-skeleton of the latter. Fishes also possess a system of median fins, supported by a special skeleton of their own. An exoskeleton of dermal spines or denticles, scales or bony plates, is usually present. Except in one group, the Dipnoi, the heart has but one auricle, and receives only venous blood, which it forces, first, through the blood-vessels of the gills, and thence, as arterial blood, through the vessels of the body generally. An air-bladder is frequently present, and serves as a hydrostatic organ or float, but in a few cases it may act as a lung, and helps the gills in the work of respiration. The paired olfactory organs rarely communicate with the oral cavity by internal nostrils. Peculiar cutaneous sense-organs are disposed in linear tracts along the sides of the body (lateral line sensory organs), and on the head, and appear to be specially associated with a life in water.

Fishes may be divided into the following "sub-classes," and these in turn may be subdivided into various "orders" and "sub-orders":—

FISHES (EXCLUSIVE OF THE SYSTEMATIC ACCOUNT OF TELEOSTEI)

CHAPTER V

FISHES
(EXCLUSIVE OF THE SYSTEMATIC ACCOUNT OF TELEOSTEI)