Fam. 1. Semionotidae.—Small-mouthed, fusiform or deep-bodied Holosteans with rhombic scales, rarely, as in Aetheolepis, cycloid in the caudal region. All the fins possess fulcra. Teeth more or less conical, with a tendency to become tritoral in certain genera. Jugular plate present or absent. Acentrophorus (Upper Permian); Semionotus (Trias of England, Germany, S. Africa, and N. America); Lepidotus (Fig. 292) (Trias of Germany, Jurassic of Europe and India, Cretaceous of Brazil); the deep-bodied Dapedius (Lias of Dorset, Fig. 293), and Aetheolepis (Jurassic of New South Wales) are characteristic genera.

Fam. 2. Macrosemiidae.—Closely related to the Semionotidae, but with a more extended dorsal fin. Macrosemius (Upper Jurassic of England, Germany, France); Notagogus (Upper Jurassic of Naples, Bavaria, France); Petalopteryx (Upper Cretaceous of Syria).

Fam. 3. Pycnodontidae.—Highly specialised deep-bodied Fishes, with a small mouth and characteristic grinding or tritoral teeth. Scales rhombic. Fulcra absent. Dorsal and anal fins long. There is no jugular plate. The family ranges from the Lower Lias to the Lower Eocene, inclusive. Mesodon, Mesturus, Gyrodus, and Microdon are Jurassic genera. Coccodus and Xenopholis occur in the Upper Cretaceous of Syria (Mount Lebanon), and Pycnodus in various European Eocene formations.

Fam. 4. Eugnathidae.—Large-mouthed, elongate fusiform predaceous Fishes, with pointed teeth, rhombic scales, short dorsal and anal fins, a single jugular plate and prominent fulcra. The vertebral centra are represented by distinct hypo- and pleuro-centra, which may form complete alternating rings in the tail.

The family first appears in the Trias and ranges throughout the Jurassic period. Eugnathus (Jurassic) and Eurycormus (Upper Jurassic). Caturus (Fig. 294) has a more extensive range, occurring in the Upper Trias of the Tyrol and in the Upper Jurassic of England and Bavaria. Caturus and Eurycormus, with their relatively thin, imbricated, cycloid scales, which have lost the peg-and-socket articulation, form connecting links between the more typical Eugnathus and the Amiidae.

Fam. 5. Amiidae.—Body fusiform and somewhat compressed. Scales uniformly thin, cycloid, and imbricated. Single dorsal fin long and low. Anal fin short. Tail nearly homocercal, with a rounded hinder margin. Fulcra absent from all the fins. Moderately large conical teeth are present on the premaxillae, maxillae, palatines and dentaries, and smaller teeth on the vomers, pterygoids, splenials and parasphenoid. Pre- and post-centra fused in the trunk, forming complete bony amphicoelous centra, but distinct in the tail. A single large jugular plate is present. In the solitary living species the air-bladder is cellular, and its afferent arteries are derived from a posterior aortic arch. Pyloric caeca absent. Two peculiar comb-like structures are present on the throat.

The Bow-Fin (Amia calva), the sole existing representative of the family, is abundant in the rivers and lakes of Central and Southern North America, including the great lakes Huron and Erie. It is a voracious, carnivorous Fish, preying upon other Fish as well as upon fresh-water Crustaceans and Insects, very tenacious of life, and of no economic value. The male is smaller than the female, about 18 inches in length, and is distinguished by the presence of a round black spot, encircled by a margin of orange, at the base of the caudal fin (Fig. 295). The female may exceed 24 inches.

Amia frequently rises to the surface, especially when the water is foul, and takes in large mouthfuls of air, and it is probable that the air is subsequently passed into the spacious cellular air-bladder which acts as a lung. The breeding season, during which the coloration of the Fish is more brilliant than at other times, lasts from the beginning of May to June, but it may begin and end somewhat earlier if the temperature be favourable. The Fish makes its way from the deeper water, where it has remained sluggish during the winter, to the spawning ground. This is usually at the swampy end of a lake where there is an abundance of aquatic herbage intersected by channels of clear water. There the Fish is said to circle round until the soft weeds and rootlets are bent and crushed aside, so as to leave an area having the appearance of a crude form of nest,^[588] in which the eggs are deposited. They may be found in enormous numbers adhering to the leaves and rootlets of the weedy home. After oviposition the male remains on guard until the young are hatched out, when they appear to leave the nest in a body, still under the protection of their watchful parent. At all events a little later the male has been observed to be accompanied by a swarm of young fry, which he keeps together by circling round them. The development of the eggs is remarkably rapid. From the first cleavage of the egg to the hatching of the embryo the whole process may be completed within from 4 to 8 days. When hatched the larvae are about 5 to 6 mm. long. They possess a large yolk sac and a preoral sucker for attachment. The pectoral fins are conspicuous structures before there is any trace of the pelvic fins.

The Amiidae, represented by Megalurus,^[589] first appear in the Upper Jurassic of Dorset, France, and Bavaria. In the Cretaceous period the family is represented by Amiopsis. Species of Amia occur in the Eocene of Europe and North America. In the former area the genus became extinct at the close of the Lower Miocene period, but in the latter Amia calva still survives.

Fam. 6. Pachycormidae.—Large-mouthed, predaceous Amioid Fishes with a more or less prominent snout and a short dorsal fin. Scales rhombic but thin, rounded behind, and overlapping, sometimes absent. A single large jugular plate.

In the earlier forms (e.g. Pachycormus, Lias) the snout is but slightly produced, but in Hypsocormus (Upper Jurassic), and especially in Protosphyraena (Cambridge Upper Greensand and the Cretaceous of Europe and North America), it becomes greatly elongated and associated with an exceptionally strong dentition.

Fam. 7. Aspidorhynchidae.—Long-bodied Fishes, with a pointed preoral rostrum, sharp teeth, and deep rhombic scales. Fins small, the dorsal and anal being remote from the pelvic fins. Fulcra vestigial or absent. Jugular plates not known.

Two genera only are known. Aspidorhynchus is a Jurassic form. Belonostomus is Upper Jurassic and Cretaceous. Species of the latter genus have a very wide distribution (Europe, North and South America, and Australia).

Fam. 8. Lepidosteidae.—Body elongate, with a relatively short caudal region. Tail semi-heterocercal. Scales rhombic, thick, ganoin-coated and articulated, not vertically elongated on the sides of the body. Dorsal and anal fins short and remote from the pelvic fins. Median fins with fulcra. Both the upper and lower jaws more or less elongated, forming a broad and depressed or a long tapering beak, near the anterior end of which the nostrils are placed. Eyes small. Vertebral centra well ossified, opisthocoelous and fused with the neural arches. The metapterygoid bones have a secondary articulation with the skull.^[590] Maxillae segmented into numerous pieces. Jugular plates absent. Branchiostegal rays reduced to three on each side. Teeth numerous, slender, and of unequal size. In the larger teeth the dentine is intricately folded. Pyloric caeca branched and compacted together into a gland-like mass. Air-bladder cellular, but its blood is not derived from a posterior aortic arch.

The only known genus is Lepidosteus, the existing species of which frequent the fresh waters of North America.^[591] The common or Long-nosed Gar-Pike (L. osseus), remarkable for its long and slender beak, is generally abundant in the rivers and lakes of the United States from Vermont to the Rio Grande, and it may reach a length of five feet. The "Short-nosed Gar" (L. platystomus, Günther) has a much shorter and broader beak, and a similar distribution (Fig. 299). The "Great" or "Alligator Gar" (L. viridis, Günther) has a more southerly habitat, frequenting the rivers of the Southern States, Northern Mexico, and Cuba. It is by far the largest species, sometimes reaching a length of 8 to 10 feet.

Lepidosteus is a voracious Fish, preying upon smaller Fishes, and, except in the breeding season, it frequents the deeper parts of the rivers or lakes. The Fish is constantly in the habit of rising to the surface and emitting bubbles of gas, either through the mouth or by the branchial clefts, and it is probable that this gas is air which has been previously swallowed at the surface and passed into the air-bladder. About May Lepidosteus resorts in large numbers to shallower water, where the temperature is higher, for the purpose of spawning, each female being attended by from one to four males.^[592] During brief recurring periods of excitement, accompanied by convulsive lashing movements, the eggs and sperm are emitted. The eggs are extremely sticky, and adhere tenaciously to the rocks and stones on which they are deposited. In a few days the embryos hatch out, and at this stage the larva has a huge mouth surmounted by a terminal preoral disc, fringed with a row of marginal wart-like suckers (Fig. 300). The yolk sac is so large as greatly to hamper the movements of the larva; hence, by means of its suckers, the young Lepidosteus attaches itself to surrounding objects, and remains almost entirely motionless for some little time after hatching. Later, about a fortnight after escaping from the egg, the yolk becomes completely absorbed, the suckers degenerate and eventually disappear, and the larva, freed from its load of nutritive reserve, assumes a more active life. After the absorption of the yolk the larvae of Mosquitos appears to form the exclusive diet of the young Lepidosteus for some time, but very soon young Fishes are readily devoured.^[593]

Lepidosteus seems to have been abundant in Europe during the Eocene and Miocene periods, but became extinct before the Pliocene. In North America, also, the genus dates from the Eocene, and still survives.

Order IV. Teleostei.

[For the account of this Order, see pp. 541 f.]

CHAPTER XIX

DIPNEUSTI

Sub-Class III. Dipneusti (Dipnoi).

These singularly interesting Fishes are distinguished by their more or less acutely lobate paired fins and their overlapping cycloid scales, and by the fact that the bony dermal fin-rays of the median fins are much more numerous than their supporting radialia. Tail heterocercal or apparently diphycercal. Nostrils inferior. Vertebral column acentrous. The radialia of the median fins articulate with the contiguous neural or haemal spines and agree with them numerically. Skull autostylic. Premaxillae and maxillae absent, but a secondary lower jaw is represented by certain dermal bones of which tooth-bearing splenials are the most important, the dentary bones being absent altogether, or, if present, toothless and small. The cranial dermal bones include median as well as paired lateral plates, but their relations to those of other Fishes are very obscure. Two opercular bones are always present, but branchiostegal rays are unknown. One of the most important diagnostic features is the dentition. All Dipneusti agree in possessing large tritoral dental plates supported by the palato-pterygoid and splenial bones. The secondary pectoral girdle includes only cleithra and infraclavicles (clavicles). There is a pelvic girdle. Claspers absent. Of the four families of Dipneusti, two, the Ctenodontidae and the Uronemidae, are exclusively Palaeozoic. The third, the Ceratodontidae, is Mesozoic, and still survives. The fourth, the Lepidosirenidae, is known only by two existing genera.

Fam. 1. Ctenodontidae.—Body fusiform. Tail heterocercal or apparently diphycercal. Excluding the anal fin, which is always distinct, the remaining median fins are either distinct or continuous. Dental plates traversed by radiating transverse ridges terminating in rows of conical denticles (ctenodont dentition, Fig. 303). Vomerine teeth not known. Cranial bones numerous and small, and, like the squamation, with or without an investment of ganoin. Jugular plates present or absent.^[594] The oldest genus is Dipterus^[595] from the Old Red Sandstone of Scotland, where it is contemporaneous with the earliest Crossopterygii and also with the oldest known Actinopterygii (Cheirolepis). Phaneropleuron (Old Red Sandstone of Scotland, Upper Devonian of Canada, Fig. 302), Scaumenacia (Upper Devonian of Canada), Ctenodus (Carboniferous of Great Britain and North America), and Sagenodus (Carboniferous of Great Britain and Lower Permian of Bohemia) belong to the same family.

Fam. 2. Uronemidae.—Body fusiform. Dentition non-ctenodont, consisting of patches of distinct rounded denticles with a row of basally-confluent conical denticles along the outer margin of each. Scales thin. All the median fins are continuous. Tail apparently diphycercal. Cranial dermal bones as in Dipterus. Uronemus^[596] (Lower Carboniferous of Scotland), and perhaps Conchopoma^[597] (Lower Permian of Prussia), are the only known genera.

The two remaining families possess certain features which cannot be affirmed to have existed in their extinct allies. Thus, both agree in exhibiting those striking and, so far as Fishes are concerned, unique modifications of the air-bladder and vascular system, and the olfactory organs,^[598] which are more or less closely associated with air-breathing habits and indicate a marked convergence towards the Amphibia. Side by side with such indications of advancing specialisation in certain directions, ample evidence of a remote ancestry is to be seen in such primitive features as the presence of a spiral valve and a multi-valvular conus arteriosus, and in the short and simple alimentary canal. Of other points of agreement mention may be made of the absence of jugular plates, the presence of vomerine teeth, the continuity of all the median fins, and the apparently diphycercal but probably gephyrocercal character of the tail.

Fam. 3. Ceratodontidae.—Body elongated and compressed. Scales large, thin, non-ganoid, and partially enclosed in dermal pouches. Paired fins biserial. Chondrocranium complete. Dermal bones wholly devoid of ganoin, reduced in number but increased in size. Circumorbital bones present. Dental plates oval, crescentic or triangular, traversed by several radiating enamelled ridges, terminating in smooth or feebly denticulated biting margins. Lower jaw with a small toothless dentary on each side. The hyoid arch includes a small hyomandibular and a hypo-hyal in addition to a cerato-hyal. Branchial arches five in number and bisegmented. The gills exhibit little evidence of degeneration. Hyo-branchial cleft open, and associated with a pseudobranch. The first four branchial arches carry holobranchs. Air-bladder single. Young not provided with cutaneous gills. Two genera only are known, the Mesozoic Ceratodus and the still living Neoceratodus. The former genus includes numerous species, for the most part known only by their dental plates, and has a remarkably wide distribution in different geological formations. Species occur in the Trias of England, Germany, India, South Africa (Upper Karoo strata), and also, but more rarely, in certain Jurassic deposits in England and in Colorado.^[599] Neoceratodus is represented by a solitary species, N. forsteri^[600] (Fig. 304, A), which is now restricted to the Burnett and Mary rivers in Queensland. A somewhat wider distribution of the species in recent times is indicated by the presence of teeth in the later Tertiary (alluvial) deposits of Darling Downs, near the borders of New South Wales.

The Neoceratodus^[601] of the Burnett frequents the comparatively stagnant pools or water-holes which alternate with shallow runs and are usually full of water all the year round. In these pools, filled with a rich growth of aquatic vegetation, and often the favourite haunt of the Platypus (Ornithorhynchus), the Fish is fairly abundant. Inactive and sluggish in its habits, usually lying motionless on the bottom, the Fish is easily captured by the natives with hand-nets or baited hooks. Neoceratodus lives on fresh-water Crustaceans, worms, and molluscs, and to obtain them it crops the luxuriant vegetation of the water-holes much in the same way that a Polychaet or a Holothurian swallows sand for the sake of the included nutrient particles. Apparently the air-bladder is a functional lung at all times, acting in conjunction with the gills. At irregular intervals the Fish rises to the surface and protrudes its snout in order to empty its lung and take in fresh air. While doing so the animal makes a peculiar grunting noise, "spouting" as the local fishermen call it, which may be heard at night for some distance, and is probably caused by the forcible expulsion of air through the mouth. Useful as the lung is as a breathing organ under normal conditions, there can be little doubt that its value as such is much greater whenever gill-breathing becomes difficult or impossible.

This seems to be the case during the hot season, when the water becomes foul from the presence of decomposing animal or vegetable matter. Semon records a striking illustration of this in the case of a partially dried-up water-hole, in which the water had become so foul that it was full of dead fishes of various kinds. Fatal as these conditions were to ordinary Fishes, Neoceratodus not only survived but seemed to be quite healthy and fresh. Such observations are of exceptional interest. Not only do they afford a clue to the conditions of life which, in the course of time, probably led to lung-breathing in Neoceratodus, but they also suggest the possibility that a similar environment has been conducive to the evolution of air-breathing Vertebrates from gill-breathing and Fish-like progenitors. In spite of its pulmonary respiration, Neoceratodus more closely resembles the typical Fishes in its habits than any other Dipneusti. It lives all the year round in the water. There is no evidence that it ever becomes dried up in the mud, or passes into a summer sleep in a cocoon, and the well-developed condition of its gills suggest that these organs play a more important rôle in breathing than in either Protopterus or Lepidosiren. The Fish is not known to leave the water, and the paired fins, useful no doubt as paddles, are quite incapable of supporting the bulky body on terra firma. In fact, when Neoceratodus is taken out of its natural element it seems to be more helpless than most other Fishes, and, in spite of its capacity for lung-breathing, soon dies unless kept moist by artificial means. Spawning takes place from April to November, principally in September and October. The eggs, invested by a jelly-like coat, secreted by the oviducal walls, are deposited not in a nest, but singly amongst aquatic vegetation, and, as they are not adherent, it is probable that they finally rest on the mud. The early developmental stages exhibit a general resemblance to those of Amphibia. There is no larval metamorphosis, and at no period does the young Neoceratodus (Fig. 305) possess cutaneous gills or a cement organ. The tail is apparently diphycercal from the first, and the pelvic limbs do not appear until about six weeks after the pectoral members. It is interesting to note that the dental plates are first represented by lines or patches of separate denticles (non-ctenodont), which subsequently fuse basally (ctenodont) before the adult condition is reached.^[602] Neoceratodus is stated to grow to a length of 5 to 6 feet.

Fam. 4. Lepidosirenidae.—Body elongate, cylindrical and more or less Eel-like, with small cycloid scales completely enclosed in the skin. Paired fins so acutely lobate as to present the appearance of tapering cylindrical filaments, equally devoid of scales and fin-rays. In a general way the cranial dermal bones correspond with those of Neoceratodus, but the place of the posterior median bone is taken by a large, gable-like fronto-parietal bone, situated internal to the head muscles, and in direct relation with the chondrocranium, which is largely aborted in the interorbital region. Circumorbital bones absent. Opercular bones much reduced. Lower jaw without dentary plates. Palatine and splenial dental plates with three non-denticulate, trenchant ridges. Hyoid arch consists of cerato-hyals only. Hyoidean cleft closed. Certain of the anterior branchial arches devoid of branchial filaments; when present the latter are leaf-like and free. Air-bladder a double lung. There is a larval metamorphosis, and the young possess cutaneous gills. The family includes two genera, Protopterus and Lepidosiren. In the former genus the paired fins are either uniserial or they consist of axial mesomeres only; there are six branchial arches and five clefts; and the larval gills are usually retained as vestiges throughout life. In Lepidosiren the paired fins are reduced to the segmented axis, without pre- or post-axial radials. There are five branchial arches and four clefts, and the cutaneous gills disappear soon after the larval metamorphosis.

Protopterus has a wide distribution over the middle portion of the great African continent, ranging from the river Senegal and the White Nile on the north to the Congo basin, Lake Tanganyika, and the Zambesi on the south. Three species are known, P. annectens (Fig. 304), P. aethiopicus, and P. dolloi. Protopterus^[603] is usually found in marshes in the vicinity of rivers. Voracious in its habits the Fish is mainly carnivorous, subsisting principally on Frogs, worms, insects, and crustaceans. It is by no means averse to preying upon its own kind, and if several of these Fishes are confined in the same aquarium they are apt to give free vent to their cannibal instincts by biting off the tails or limbs of their fellows. The missing parts are soon regenerated, but the new members are usually somewhat abnormal, the tail, for instance, never regaining its original length, while a new pectoral limb may be bifid or even trifid.^[604] The tail is the principal organ of locomotion, and by its means the Fish is capable of remarkably quick, agile movements. When slowly moving over the bottom of an aquarium the paired limbs are observed to move to and fro on opposite sides alternately in a somewhat bipedal fashion. The limbs are useless for swimming, although it is possible that they may be helpful in creeping over the bottom, or in balancing, or as tactile organs. Protopterus is said to breathe by its lungs as well as by its gills, and to rise to the surface at short intervals to take in fresh air.

In the dry seasons the marshes in which Protopterus lives become dried up, and to meet this adverse change in its surroundings the Fish hibernates, or passes into a summer sleep, until the next rainy season brings about conditions more favourable to active life. Preparatory to this summer sleep, and before the ground becomes too hard, the Fish makes its way into the mud to a depth of about 18 inches, and there coils itself up in a flask-like enlargement (Fig. 307) at the bottom of the burrow, which is lined by a capsule of hardened mucus secreted by the glands of the skin.^[605] The mouth of the flask is closed by the capsular wall or lid, which is perforated by a small aperture. The margins of this aperture are pushed inwards, so as to form a tubular funnel for insertion between the lips of the Fish. While encapsuled in its cocoon the Fish is surrounded by a soft slimy mucus, no doubt for the purpose of keeping the skin moist, and its lungs are the sole breathing organs, the air passing from the open mouth of the burrow through the hole in the lid directly to the mouth of the animal. The nutrition of the dormant Fish is effected by the absorption of the fat stored up about the kidneys and gonads, somewhat after a fashion not unknown in the fat-bodies of Insects and the hibernating glands of Rodents. Even portions of the caudal muscles undergo fatty degeneration, and thus, in a way which recalls the mode of nutrition of the Salmon during the breeding season, and of the Tadpole during its metamorphosis, a further store of nutritive material becomes available for the sustenance of the Fish during its long summer nap. It is highly probable that the exceptionally numerous leucocytes act as carriers in the work of transporting the fatty particles to the different organs and tissues of the body. The length of the summer sleep naturally varies with the duration of the dry season, and probably it lasts on an average nearly half the year (August to December). The cocoons, imbedded in an outward casing of hardened mud, have often been brought to Europe, and when placed in water of suitable temperature the long torpid Protopterus escapes from its prison in a perfectly healthy condition, and resumes its partly branchial and partly pulmonary mode of breathing. The negroes of the West Coast of Africa are very partial to these Fishes, which they dig out of the dried marshes and preserve in their clumps of mud for food. With the advent of the rainy season, when the marshes become flooded, the Protopterus emerges from its cocoon, and returning to its former active life, soon enters upon the task of reproducing its kind. The important observations of Budgett^[606] have thrown much light on the curious breeding habits and development of these Fishes. The Fish makes a nest near the edge of a swamp. The nest is simply a hole of irregular shape, about a foot in depth, filled with water and surrounded by long grass (Fig. 308). There is no lining to the nest, and the eggs are deposited on the bare mud. Until the eggs are hatched, which occurs about the eighth day, and while the larvae are in the nest, the male remains on guard, and is apt to bite severely an incautious intruder. Probably with the view of aerating the eggs the water is continually lashed about by the tail of the guardian parent. The male has no trace of the peculiar vascular filaments which adorn the pelvic limbs of the male Lepidosiren during the breeding season. The early developmental stages are similar in their main outlines to those of Neoceratodus, but the young are very different. When the young Protopterus (Fig. 309) is hatched it is provided with a crescentic glandular sucker or cement-organ, situated on the under side of the head behind the mouth, by means of which the larva attaches itself to the sides of the nest, or of the vessel in which it is confined, much in the same way as the young Lepidosteus, and probably for the same reason. It may be remarked that the sucker agrees in structure, position, and function with that found in Amphibian tadpoles, but it differs both in position and structure from its preoral analogue in the young of Acipenser, Amia, and Lepidosteus.

A month-old larva has much the aspect of a larval Newt. It has four pairs of vascular plumose cutaneous gills (Fig. 309), which are retained as vestiges for a long time or even throughout life, and two pairs of synchronously-developed limbs. As an interesting instance of a nocturnal and protective change of colour, it may be mentioned that the dark chromatophores of the skin of the larva expand in the day-time and the young Fish becomes darker in colour, and therefore less conspicuous when seen against a background of black mud or soil. At night the contraction of the colour-sacs renders the larva more transparent and probably less easily visible than if opaque. The commencement of pulmonary respiration is coincident with the degeneration of the cutaneous gills, which takes place about seven weeks after the deposition of the eggs, and about a month after the larvae leave the nest. Protopterus is said to attain a length of six feet.

Lepidosiren paradoxa,^[607] probably the only species of the genus, is confined to South America. It occurs along the course of the main Amazon river, entering some of its larger affluents, such as the Ucayale, the Madeira, the Rio Negro, and the Tapajóz, and also in the Chaco Boreal to the west of the Upper Paraguay river. The home of the Lepidosiren (or "Lolach," as the natives call the Fish) of the Chaco country is to be found in the wide-spreading marshes and swamps, which for a great part of the year are almost choked by a luxuriant growth of their own peculiar vegetation and covered by a floating carpet of surface weeds, with here and there deeper and clearer water and slow-flowing streams. In the dry season the water gradually shrinks and the swamps eventually become dried up. Of sluggish habits, the Fish wriggles slowly about at the bottom of the swamp like an Eel, using its hind limbs in an irregular bipedal fashion as it wends its way through the dense network of subaqueous plants. Lepidosiren is not exclusively carnivorous. The large fresh-water snail, Ampullaria, which lives in the swamps in enormous numbers, seems to be its favourite food; but masses of confervoid Algae are also eaten, and in its earlier stages it is probable that the Fish is more herbivorous than carnivorous. The Jacare (Caiman sclerops) feeds on Lepidosiren, and this fact, and probably also the cannibal habits of the Fish itself, may explain the capture of specimens with mutilated tails and regenerated, branched, pectoral limbs. Like other living Dipneusti, Lepidosiren rises to the surface to breathe. The intervals are, however, very variable, and no doubt depend on the relative purity or impurity of the water. Both expiration and inspiration are said to take place through the mouth. The snout is protruded on the surface, and the creature expires. After being withdrawn for a moment the head is again projected, and inspiration takes place through the partially open lips.

When the Fish finally sinks a few bubbles of surplus air escape through the gill-clefts. A nocturnal and protective change of colour, similar to that described in Protopterus, has been observed, and although most strikingly manifest in the larvae, it also occurs in individuals of older growth. The flesh is much esteemed as food by the Indians, who wade into the swamps and transfix the Fishes with spears. During the rainy season the Lepidosiren eats voraciously, and a reserve of fat is stored up in the tissues. Like its African relative, the Fish ceases to feed on the approach of the dry season, and eventually hibernates at the dilated extremity of a deep tubular burrow, the entrance to which is plugged by a small lump of clay perforated by several round holes. On the rising of the water at the next rainy season the Lepidosiren pushes out the plug and soon emerges from its burrow.^[608] The breeding season begins soon after the escape of the Fish. The eggs are deposited in nests in the form of underground burrows excavated in the black peaty soil at the bottom of the swamp, with an entrance about 4-5 inches wide. At a depth of about a foot the burrow takes a horizontal course, its total length varying from 2-5 feet. After the eggs are laid the male remains to guard them. During the breeding season the pelvic limbs of the male enlarge and become covered by a rich growth of highly vascular, blood-red filaments 2-3 inches in length^[609] (Fig. 310). The use of these curious structures is uncertain, but it is not improbable that they act as accessory gills to enable the male to guard the eggs in the nest without being forced to resort to the surface to breathe air. The development is essentially similar to that of Protopterus. The larva (Fig. 311) has four pairs of cutaneous gills in relation with the first, second, third, and fourth branchial arches, inclusive, the first three pairs being the homologues of the cutaneous gills of the tailed Amphibia; and also a cement-organ which disappears shortly before the larval metamorphosis. At that period the circulation in the cutaneous gills becomes sluggish, and very soon these organs completely atrophy. About the same time the hyo-branchial cleft closes up, as in Protopterus. The young Lepidosiren soon begins to breathe air and to become more active and lively in its habits.^[610] The adult may attain a length of four feet.

The relations of the different genera of Dipneusti to one another has been discussed by Dollo in a remarkably suggestive paper.^[611] Until the publication of this treatise it was generally believed that the modern Dipneusti, Neoceratodus, Protopterus, and Lepidosiren, especially the first mentioned, were the most primitive and the more nearly related to the ancestral stock, while the older types, such as Dipterus, were regarded in the light of highly specialised offshoots. The continuity of the median fins, the apparently diphycercal character of the tail, and the wholly cartilaginous condition of the chondrocranium in the modern Dipneusti, were contrasted with the divided median fins, the heterocercal tail, and the more extensively ossified chondrocranium of the Palaeozoic forms, and the belief seemed inevitable. Dollo has shown, however, that there is good reason for the view that the evolution of the group has taken place in exactly the opposite direction; that, in fact, the older Dipneusti are the more archaic, and that their modern representatives have been derived from them by a sequence of retrogressive changes; or, in other words, the latter have much the same relation to the former as the degenerate Sturgeons and Paddle-Fishes to their Palaeozoic ancestors, the Palaeoniscidae. Taking Dipterus, the most ancient of all the known Dipneusti, as a starting-point, it is possible to select a series of genera which illustrate the evolution of the group both in structure and in palaeontological sequence.^[612] The series is as follows:—Dipterus, Scaumenacia, Phaneropleuron, Uronemus, Ceratodus (Neoceratodus), Protopterus and Lepidosiren. Briefly, the more important structural modifications observable in the transition from the older to the recent genera are (a) the gradual union of isolated median fins to form a continuous fin^[613]; (b) the substitution of a gephyrocercal tail for a heterocercal^[613]; (c) the degeneration of the squamation, the thick ganoid scales of the earlier types being replaced by thin, non-ganoid scales; (d) a reduction in the number of cranial dermal bones and the loss of their original ganoid investment; (e) the suppression of the jugular plates; and (f) a reduction in the size of the opercular bones. In the last two genera of the series, in which specialisation in some respects and degeneration in others have reached their maximum, the body no longer retains the fusiform and more typically Fish-like shape of the older genera, but, in accordance with Eel-like habits and mode of progression, has become more or less Eel-like in form.^[614] The paired fins are almost vestigial, while the scales, so deeply insunken in the skin as to be externally invisible, suggest that the modern Dipneusti are approximating to a final scaleless as well as to an ultimately limbless condition. As to the origin of the Dipneusti as a group, it seems reasonable to look for their ancestors in the early Devonian Crossopterygii with acutely lobate fins, or, with greater probability, to some still more primitive Crossopterygian with simple, non-rhizodont teeth, capable by fusion of giving rise to massive tritoral plates, and involving as a consequence the substitution of an autostylic for an originally hyostylic skull, and the suppression of the secondary upper jaw. In fact, when our knowledge of the development of the surviving Dipneusti and Crossopterygii is more complete, it is not improbable that the inclusion of the two series of Fishes in subordinate divisions of the Teleostomi will prove to be amply justified. The relations of the Dipneusti to the Amphibia are somewhat deceptive, and it seems improbable that the former group stands in the direct line of Amphibian descent. In most of their structural features not directly or remotely associated with air-breathing the Dipneusti are true Fishes, and the striking resemblances which they present to the Amphibians in the vascular system and lungs seem to be rather the outcome of physiological convergence, associated with adaptive and parallel modifications in structure, and due to the influence of a similar environment, than indicative of direct ancestral relations. With more reason it may be inferred that both the Dipneusti and the Amphibia have been derived from some primitive Crossopterygian ancestor with Elasmobranch tendencies, and subsequently became modified in certain respects on parallel lines.