Pristis.—Body depressed and elongate, gradually passing into the strong and muscular tail. Pectoral fins, with the front margins quite free, not extending to the head. No tentacles below the saw. Teeth in the jaws minute, obtuse. Dorsal fins without spine, the first opposite or close to the base of the ventrals.

“Saw-fishes.” Abundant in tropical, less so in sub-tropical seas. They attain to a considerable size, specimens with a saw 6 feet long and 1 foot broad at the base not being of uncommon occurrence. The saw, which is their weapon of attack, renders them most dangerous to almost all the other large inhabitants of the ocean. Its endoskeleton consists of three, sometimes five, rarely four, hollow cylindrical tubes, placed side by side, tapering towards the end, and incrusted with an osseous deposit. These tubes are the rostral processes of the cranial cartilage, and exist in all Rays, though in them they are shorter and much less developed. The teeth of the saw are implanted in deep sockets of the hardened integument. The teeth proper, with which the jaws are armed, are much too small for inflicting wounds or seizing other animals. Saw-fishes use this weapon in tearing pieces of flesh off an animal’s body or ripping open its abdomen. The detached fragments or protruding soft parts are then seized by them and swallowed. Five distinct species of Saw-fishes are known.

Saws of extinct species have been found in the London clay of Sheppey and in the Bagshot sands.

Second Family—Rhinobatidæ.

Tail strong and long, with two well-developed dorsal fins, and a longitudinal fold on each side; caudal developed. Disk not excessively dilated, the rayed portion of the pectoral fins not being continued to the snout.

Rhynchobatus.—Dorsal fins without spine, the first opposite to the ventrals. Caudal fin with the lower lobe well developed. Teeth obtuse, granular, the dental surfaces of the jaws being undulated.

Fig. 125.—Dentition of Rhynchobatus.

Two species, Rh. ancylostomus and Rh. djeddensis, are very common on the tropical coasts of the Indian Ocean. They feed on hard-shelled animals, and attain scarcely a length of 8 feet.

Rhinobatus.—Cranial cartilage produced into a long rostral process, the space between the process and pectoral fin being filled by a membrane. Teeth obtuse, with an indistinct transverse ridge. Dorsal fins without spine, both at a great distance behind the ventral fins. Caudal fin without lower lobe.

Numerous on the coasts of tropical and sub-tropical seas; about twelve species. Trygonorhina is an allied genus from South Australia.

The oolitic genus Spathobatis is scarcely distinct from Rhinobatus; and another fossil from Mount Lebanon has been actually referred to this latter genus. Trigorhina from Monte Postale must be placed here.

Third Family—Torpedinidæ.

The trunk is a broad, smooth disk. Tail with a longitudinal fold on each side; a rayed dorsal fin is generally, and a caudal always, present. Anterior nasal valves confluent into a quadrangular lobe. An electric organ composed of vertical hexagonal prisms between the pectoral fins and the head.

“Electric Rays.” The electric organs with which these fishes are armed are large, flat, uniform bodies, lying one on each side of the head, bounded behind by the scapular arch, and laterally by the anterior crescentic tips of the pectoral fins. They consist of an assemblage of vertical hexagonal prisms, whose ends are in contact with the integuments above and below; and each prism is subdivided by delicate transverse septa, forming cells, filled with a clear, trembling, jelly-like fluid, and lined within by an epithelium of nucleated corpuscles. Between this epithelium and the transverse septa and walls of the prism there is a layer of tissue on which the terminations of the nerves and vessels ramify. Hunter counted 470 prisms in each battery of Torpedo marmorata, and demonstrated the enormous supply of nervous matter which they receive. Each organ receives one branch of the Trigeminal nerve and four branches of the Vagus, the former, and the three anterior branches of the latter, being each as thick as the spinal chord (electric lobes). The fish gives the electric shock voluntarily, when it is excited to do so in self-defence or intends to stun or to kill its prey; but to receive the shock the object must complete the galvanic circuit by communicating with the fish at two distinct points, either directly or through the medium of some conducting body. If an insulated frog’s leg touches the fish by the end of the nerve only, no muscular contractions ensue on the discharge of the battery, but a second point of contact immediately produces them. It is said that a painful sensation may be produced by a discharge conveyed through the medium of a stream of water. The electric currents created in these fishes exercise all the other known powers of electricity: they render the needle magnetic, decompose chemical compounds, and emit the spark. The dorsal surface of the electric organ is positive, the ventral surface negative.

[The literature on the electric organ of Torpedo is very extensive. Here may be mentioned Lorenzini, “Osservazioni intorno alle Torpedini,” (1678); Walsh, “On the Electric Property of the Torpedo,” in Philos. Trans., 1773; Hunter, “Anatomical Observations on the Torpedo,” ibid.; Davy, “Observations on the Torpedo,” in Philos. Trans., 1834; Matteucci and Savi, “Traité des Phénomènes Electro-Physiologiques,” 1844.]

Of the genus Torpedo six species are known, distributed over the Atlantic and Indian Oceans; three of them are rather common in the Mediterranean, and one (T. hebetans) reaches the south coast of England. They attain to a width of from two to three feet, and specimens of that size are able to disable by a single discharge a full-grown man, and, therefore, may prove dangerous to bathing persons. Other genera, differing from Torpedo in the position and structure of some of the fins, are found in other tropical and sub-tropical seas, viz. Narcine, Hypnos, Discopyge (Peru), Astrape, and Temera. All, like electric fishes generally, have a naked body.

A large fish, of the general appearance of a Torpedo, has been found at Monte Bolca; and Cyclobatis, from the upper cretaceous limestone of Lebanon, is probably another extinct representative of this family.

Fourth Family—Rajidæ.

Disk broad, rhombic, generally with asperities or spines; tail with a longitudinal fold on each side. The pectoral fins extend to the snout. No electric organ; no serrated caudal spine.

Raja.—Two dorsal fins on the tail, without spine; tail with a rudimentary caudal fin, or without caudal. Each ventral fin divided into two by a deep notch. Teeth small, obtuse, or pointed. Pectoral fins not extending forwards to the extremity of the snout. Nasal valves separated in the middle, where they are without a free margin (see Fig. 1, p. 34).

Fig. 126.—Raja lemprieri, from Tasmania.

Fig. 127.—Dermal spines of a male Thornback, Raja clavata.

Of all the genera of Batoidei, Rays have the widest geographical range; they are chiefly inhabitants of temperate seas, and much more numerous in those of the Northern than of the Southern Hemisphere. They advance more closely to the Arctic and Antarctic circles than any other member of this group. More than thirty species are known, of which the following are found on the British coast:—The Thornback (R. clavata), the Homelyn Ray (R. maculata), the Starry Ray (R. radiata), the Sandy Ray (R. circularis), the common Skate (R. batis), the Burton Skate (R. marginata), and the Shagreen Skate (R. fullonica). Some of these species, especially the Skates, attain a considerable size, the disk measuring six and even seven feet across. All are eatable, and some of them regularly brought to market. In the majority of the species peculiar sexual differences have been observed. In some, as in the Thornback, all or some of the teeth are pointed in the male sex, whilst they are obtuse and flat in the female. The males of all are armed with patches of claw-like spines, retractile in grooves of the integument, and serially arranged occupying a space on the upper side of the pectoral fin near the angle of the disk, and frequently also the sides of the head. In species which are armed with bucklers or asperities it is the female which is principally provided with these dermal productions, the male being entirely or nearly smooth. Also the colour is frequently different in the two sexes.

Other genera of this family are Psammobatis, Sympterygia, and Platyrhina. Although probably this family was well represented in cretaceous and tertiary formations, the remains found hitherto are comparatively few. Arthropterus, from the Lias, seems to have been a true Ray; and dermal spines of a species allied to the Thornback (Raja antiqua) are abundant in the crag deposits of Suffolk and Norfolk.

Fifth Family—Trygonidæ.

The pectoral fins are uninterruptedly continued to, and confluent at, the extremity of the snout. Tail long and slender, without lateral longitudinal folds; vertical fins none, or imperfectly developed, often replaced by a strong serrated spine.

The “Sting-Rays” are as numerous as the Rays proper, but they inhabit rather tropical than temperate seas. The species armed with a spine use it as a weapon of defence, and the wounds inflicted by it are, to man, extremely painful, and have frequently occasioned the loss of a limb. We have mentioned above (p. 190) that the danger arises from the lacerated nature of the wound as well as from the poisonous property of the mucus inoculated. The spines (Fig. 98, p. 190) are always barbed on the sides, and may be eight or nine inches long in the larger species. They are shed from time to time, and replaced by others growing behind the one in function, as the teeth of the fishes of this order, or as the fangs of a poisonous snake. Fossil species of Trygon and Urolophus occur in the tertiary strata of Monte Bolca and Monte Postale. The genera into which the various species have been divided are the following:—

Urogymnus.—Tail long, without fin or spine, sometimes with a narrow cutaneous fold below. Body densely covered with osseous tubercles. Teeth flattened.

Only one species is known (U. asperrimus), common in the Indian Ocean, and with a body from 4 to 5 feet long; the skin is frequently used for covering shields and the handles of swords and other weapons, its rough surface offering a firm hold to the hand.

Trygon.—Tail very long, tapering, armed with a long arrow-shaped barbed spine. Body smooth or with tubercles. Nasal valves coalescent into a quadrangular flap. Teeth flattened.

Some twenty-five species are known, one of which (T. pastinaca) extends from the south coast of England and the east coast of North America through the Atlantic and Indian Ocean to Japan. The majority of the species belong to the tropical parts of the Indian and Atlantic Oceans; some inhabit exclusively freshwaters of eastern tropical America. A closely allied genus is Tæniura, with six species.

Urolophus.—Tail of moderate length, with a distinct rayed terminal fin, armed with a barbed spine, without or with a rudimentary dorsal fin. Teeth flattened.

Seven species from tropical seas, apparently of small size.

Fig. 128.—Urolophus cruciatus, from Australia.

Pteroplatea.—Body at least twice as broad as long; tail very short and thin, without or with a rudimentary fin, and with a serrated spine. Teeth very small, uni- or tri-cuspid.

Six species from temperate and tropical seas.

Sixth Family—Myliobatidæ.

The disk is very broad, in consequence of the great development of the pectoral fins, which, however, leave the sides of the head free, and reappear at the extremity of the snout as a pair of detached (cephalic) fins. Viviparous.

“Devil-fishes,” “Sea-devils,” or “Eagle-rays.” Generally of large size, inhabiting temperate and tropical seas. Some genera possess a pair of singular cephalic processes, which generally project in a direction parallel to the longitudinal axis of the body, but are said to be flexible in the living fish, and used for scooping food from the bottom and conveying it to the mouth. In all the species the dentition consists of perfectly flat molars, forming a kind of mosaic pavement in both the upper and lower jaws: a most perfect mechanical arrangement for crushing alimentary substances.

Fig. 129.—Jaws of an Eagle-Ray, Myliobatis aquila.

Myliobatis.—Teeth sexangular, large, flat, tessellated, those in the middle much broader than long; several narrower series on each side. Tail very long and thin, with a dorsal fin near its root; generally a serrated spine behind the fin.

Seven species are known, two of which are European, one (M. aquila) being almost cosmopolitan, and occasionally found on the British coast. The young differ much from the adult, having no median series of larger teeth, but all the teeth of equal size and regularly sexangular. Also the tail is much longer in young examples than in old ones, and the coloration more ornamental. Teeth of species very closely allied to, or perhaps even identical with, existing species, are found in tertiary formations.

Aëtobatis.—Form of the head, body, and tail as Myliobatis. The nasal valves remain separate, each forming a long flap. The lower dental lamina projects beyond the upper. Teeth flat, broad, forming a single series, equivalent to the median series of Myliobatis, there being no small lateral teeth.

Fig. 130.—Aëtobatis narinari.

One species only (A. narinari) which is found in almost all tropical seas, and of exceedingly common occurrence in the Atlantic and Indian Oceans; it does not seem to grow to a very large size (perhaps not exceeding 5 feet in width), and is readily recognised by numerous round bluish-white spots, with which the back is ornamented. Fossils of this genus occur in the English Eocenes and the Swiss Molasse.

Fig. 131.—Aëtobatis subarcuatus, from Bracklesham.

Rhinoptera.—The cephalic appendages are bent inwards, and situated at the lower side of the snout. Nasal valves confluent into a broad flap, with free margin. Teeth broad, flat, tessellated, in five or more series, the middle being the broadest, and the others decreasing in width outwards. Tail very slender, with a dorsal fin before the serrated spine.

Fig. 132.—Rhinoptera woodwardi; fossil.

Fig. 133.—Rhinoptera polyodon.

Seven species from tropical and sub-tropical seas are known; of Rhinoptera polyodon nothing is known except the jaws; and as its dentition is very peculiar, no opportunity should be lost of obtaining and preserving entire animals. Teeth very similar to those of existing species, and described as Zygobatis, occur in the Norwich Crag and in Miocene formations of Switzerland.

Dicerobatis (Cephaloptera).—Cephalic appendages pointing straight forwards or inwards. Nostrils widely separated from each other. Mouth inferior, wide. Both jaws with very numerous and very small flat or tubercular teeth. Tail very slender, with a dorsal fin between the ventrals, and with or without a serrated spine.

Ceratoptera.—Cephalic appendages pointing forwards or inwards. Mouth anterior; wide. Teeth in the lower jaw only, very small. Tail very slender, with a dorsal fin between the ventrals and without spine.

Fig. 134.—Dicerobatis draco, from Misol.

The species of these two last genera are not yet well distinguished; about five of Dicerobatis and two of Ceratoptera are known from tropical and temperate seas, but their occurrence in the latter is rather sporadic. Some of them, if not all, attain an enormous size. One mentioned by Risso, taken off Messina, weighed 1250 pounds. Several observers speak of having seen them in pairs, the male being usually the smaller. Of a pair mentioned by Risso the female was first taken, and the male remained hovering about the boat for three days, and was afterwards found floating dead on the surface. Still larger individuals, but of uncertain species, are mentioned by Lacépède, who says that one taken at Barbadoes required seven yoke of oxen to draw it. A sketch of another, which was said to be twenty feet long, was sent to Lacépède; and Sonnini speaks of one which appeared to him to be longer and wider than the ship in which he was sailing. A fœtus taken from the uterus of the mother captured at Jamaica, and preserved in the British Museum, is five feet broad, and weighed twenty pounds. The mother measured fifteen feet in width as well as in length, and was between three and four feet thick. The capture of “Devil-fishes” of such large size is attended with danger, as they not rarely attack and capsize the boat. They are said to be especially dangerous when they accompany their young, of which they bring forth one only at a time.

SECOND SUB-ORDER—HOLOCEPHALA.

One external gill-opening only, covered by a fold of the skin, which encloses a rudimentary cartilaginous gill-cover; four branchial clefts within the gill-cavity. The maxillary and palatal apparatus coalescent with the skull.

This suborder is represented in the living fauna by one family only, Chimæridæ; it forms a passage to the following order of fishes, the Ganoids. In external appearance, and with regard to the structure of their organs of propagation, the Chimæras are Sharks (See Fig. 96, p. 184). The males are provided with “claspers” in connection with the ventral fins, and the ova are large, encased in a horny capsule, and few in number; and there is no doubt that they are impregnated within the oviduct, as in Sharks. Chimæras are naked, but, as in Scylliidæ, very young individuals possess a series of small “placoid” spines, which occupy the median line of the back, and remind us of similar dermal productions in the Rays. The males, besides, are provided with a singular erectile appendage, spiny at its extremity, and received in a groove on the top of the head. On the other hand, the relations of the Chimæras to the Ganoid, and, more especially, Dipnoous type become manifest in their notochordal skeleton and continuity of cranial cartilage. The spine in front of the first dorsal fin is articulated to the neural apophysis, and not merely implanted in the soft parts, and immovable as in Sharks. A cartilaginous operculum makes its appearance, and the external gill-opening is single. The dentition is that of a Dipnoid, each “jaw” being armed with a pair of broad dental plates, with the addition of a pair of smaller cutting teeth in the upper “jaw.” Fossils of similar dental combination are not rare in strata, commencing from the Lias and the bottom of the Oolitic series; but it is impossible to decide in every case whether the fossil should be referred to the Holocephalous or Dipnoous type. According to Newberry, Chimæroid fishes commence in the Devonian with Rhynchodus, the remains of which were discovered by him in Devonian rocks of Ohio. Undoubted Chimæroids are Elasmodus, Psaliodus, Ganodus, Ischyodus, Edaphodon, and Elasmognathus, principally from mesozoic and tertiary formations. Very similar fossils occur in the corresponding strata of North America. A single species of Callorhynchus has been discovered by H. Hector in the Lower Greensand of New Zealand.

The living Chimæras are few in number, and remain within very moderate dimensions, probably not exceeding a length of five feet, inclusive of their long filamentous, diphycercal tail. They are referred to two genera.

Chimæra.—Snout soft, prominent, without appendage. The dorsal fins occupying the greater part of the back, anterior with a very strong and long spine. Longitudinal axis of the tail nearly the same as that of the trunk, its extremity being provided with a low fin above and below, similar in form to a dorsal and anal fin. Anal fin very low.

Three species are known: Ch. monstrosa, from the coasts of Europe and Japan and the Cape of Good Hope; Ch. colliei from the west coast of North America; and Ch. affinis from the coast of Portugal. (See Fig. 96, p. 184.)

Callorhynchus.—Snout with a cartilaginous prominence, terminating in a cutaneous flap. Two dorsal fins, the anterior with a very strong and long spine. Extremity of the tail distinctly turned upwards, with a fin along its lower edge, but without one above. Anal fin close to the caudal, short and deep.

One species (C. antarcticus) is common in the Southern temperate zone. Cunningham describes the egg (see Fig. 81, p. 169), as being of a dark greenish-black colour, and, in general, measuring from eight to nine or even ten inches in length, by about three in breadth. It consists of a central, somewhat spindle-shaped convex area (between the horny walls of which the young fish lies), surrounded by a broad plicated margin, which is fringed at the edge, and covered on the under surface with fine light brownish-yellow hairs.

SECOND ORDER—GANOIDEI.

Skeleton cartilaginous or ossified. Body with medial and paired fins, the hinder pair abdominal. Gills free, rarely partially attached to the walls of the gill-cavity. One external gill-opening only on each side; a gill-cover. Air-bladder with a pneumatic duct. Ova small, impregnated after exclusion. Embryo sometimes with external gills.

To this order belong the majority of the fossil fish remains of palæozoic and mesozoic age, whilst it is very scantily represented in the recent fauna, and evidently verging towards total extinction. The knowledge of the fossil forms, based on mere fragments of the hard parts of the body only, is very incomplete, and therefore their classification is in a most unsatisfactory state. In the following pages only the most important groups will be mentioned.

[For a study of details we have to refer to Agassiz, “Poissons Fossiles;” Owen, “Palæontology,” Edinb. 1861, 8vo; Huxley, “Preliminary Essay upon the Systematic Arrangement of the Fishes of the Devonian Epoch,” in Mem. Geolog. Survey, Dec. 10; Lond. 1861, and “Illustrations of the Structure of Crossopterygian Ganoids,” ibid. December 12, 1866; Traquair, “The Ganoids of the British Carboniferous Formations,” part I. “Palæoniscidæ.” Palæontogr. Soc. Lond. 1877.]

Eight suborders may be distinguished at present.

FIRST SUB-ORDER—PLACODERMI.

Extinct. The head and pectoral region of the body encased in great bony, sculptured plates, with dots of enamel; the remainder of the body naked, or with ganoid scales; skeleton notochordal.

Comprises the oldest vertebrate remains, from Devonian and Carboniferous formations. Pterichthys: (Figs. 135 and 136), tail tapering, covered with small ganoid scales, without caudal fin; the cephalic shield was probably moveably joined to the cuirass of the trunk, and both were composed of several pieces; the abdominal shield consisted of one single median plate, and two pairs of lateral plates, a third small pair being sometimes observed detached in front of the anterior pair; pectoral exceedingly long, consisting of two pieces movably connected with each other; tail scaly, and short; a small dorsal fin placed on the tail; a pair of small ventrals; jaws small, with confluent denticles. Several species have been distinguished in remains found in the strata of Caithness and other localities in Scotland. Coccosteus (Fig. 137, p. 354): all the bony plates are firmly united, no pectoral spines; tail naked and long; a dorsal and anal fin supported by interneural and interhæmal spines. Dentition unknown. Dinichthys: a gigantic fish from the Devonian of North America (estimated at from 15 to 18 feet in length), with the dermal covering very similar to that of Coccosteus, but with a simple arched dorsal shield. As in this latter genus the caudal extremity does not possess external or internal bony parts, and the ventral plastron of both genera corresponds in every particular; the dentition is so singularly like that of Lepidosiren, that Newberry (Geolog. Survey of Ohio, vol. ii. part 2) considers this genus to be in genetic relation to the Dipnoi. The following genera have been united in a separate family, Cephalaspidæ; viz. Cephalaspis: head covered by a continuous shield with tubercular surface, produced into a horn at each posterior corner; a median dorsal backward prolongation bears a spine; heterocercal. Auchenaspis and Didymaspis: allied to the preceding, but with the cephalic shield divided into a larger anterior and smaller posterior piece. Pteraspis: with the cephalic shield finely striated or grooved, composed of seven pieces. Scaphaspis and Cyathaspis: with the surface of the head-shield similarly sculptured as in Pteraspis, but simple in the former, and composed of four pieces in the latter. Astrolepis: attained to the gigantic size of between twenty and thirty feet; its mouth was furnished with two rows of teeth, of which the outer ones were small, the inner much larger.

Fig. 135.—Dorsal surface of Pterichthys, after Pander. d, Dorsal fin; c, pectoral member; 2–10, head-bucklers; 11–13, dorsal bucklers.

Fig. 136.—Ventral aspect of Pterichthys, after Pander. 15, mandible (?); 16–21, ventral bucklers.

Fig. 137.—Coccosteus, after Pander. A, Anal fin; D, Dorsal fin; C, Heterocercal tail; c, notochord; n, neurals; h, hæmals; 6–24, bucklers.

[See Ray Lankester, A. Monograph of the Fishes of the Old Red Sandstone of Britain. Part I. Cephalaspidæ. Lond. 1868 and 1870. 4to.]

SECOND SUB-ORDER—ACANTHODINI.

Extinct. Body oblong, compressed, covered with shagreen; skull not ossified; caudal heterocercal. Large spines, similar to those of Chondropterygians, in front of some of the median and paired fins. The spines are imbedded between the muscles, and not provided with a proximal joint.

Acanthodes, Chiracanthus, from Devonian and Carboniferous formations.

THIRD SUB-ORDER—DIPNOI.

Nostrils two pairs, more or less within the mouth; limbs with an axial skeleton. Lungs and gills. Skeleton notochordal. No branchiostegals.[38]

First Family—Sirenidæ.

Caudal fin diphycercal; no gular plates; scales cycloid. A pair of molars, above and below, and one pair of vomerine teeth.

Lepidosiren.—Body eel-shaped, with one continuous vertical fin. Limbs reduced to cylindrical filaments, without fringe. Vomerine teeth conical, pointed. Each dental lamina or molar with strong cusps, supported by vertical ridges. No external branchial appendages; five branchial arches, with four intervening clefts. Conus arteriosus with two longitudinal valves. Ovaries closed sacs.

One species only is known from the system of the River Amazons (L. paradoxa). It must be very locally distributed, as but a few specimens have been brought to Europe, and all recent endeavours to obtain others have been unsuccessful. Natterer, by whom this most interesting fish was discovered, states that he obtained two specimens, one on the Madeira River, near Borba; the other in a backwater of the Amazons, above Villa Nova. The natives of the former place called it Carámurú, and considered it very scarce. The larger individual was nearly four feet long. It is said to produce a sound not unlike that of a cat, and to feed on the roots of mandioca and other vegetables. But, to judge from the dentition, this fish is much more likely to be carnivorous, like the following. It is one of the greatest desiderata of Natural History Collections.

[Natterer, “Annalen des Wiener Museum’s,” 1839, ii.; Bischoff. “Annales des Sciences Naturelles,” 1840. xiv.]

Protopterus.—Very similar in the general form of the body and dentition to Lepidosiren. Pectoral and ventral filaments with a fringe containing rays. Three small branchial appendages above the small gill-opening; six branchial arches, with five intervening clefts. Conus arteriosus with two longitudinal valves. Ovaries closed sacs.

Protopterus annectens is the “Lepidosiren” which is commonly found in Zoological collections. It is usually imported from the west coast of Africa, where it abounds in many localities; but it is spread over the whole of tropical Africa, and forms in many districts of the central parts a regular article of food.

Fig. 138.—Protopterus annectens. g, Branchial filaments; v, vent.

During the dry season, specimens living in shallow waters which periodically dry up, form a cavity in the mud, the inside of which they line with a protecting capsule of mucus, and from which they emerge again when the rains refill the pools inhabited by them. Whilst they remain in this torpid state of existence, the clay-balls containing them are frequently dug out, and if the capsules are not broken, the fishes imbedded in them can be transported to Europe, and released by being immersed in slightly tepid water. Protopterus is exclusively carnivorous, feeding on water-insects, frogs, and fishes, and attains a length of six feet.

[Owen, “Trans. Linn. Soc.” 1841, xviii.]

Ceratodus.—Body elongate, compressed, with one continuous vertical fin. Limbs paddle-shaped, with broad, rayed fringe. Vomerine teeth incisor-like; molars with flat, undulated surface, and lateral prongs. No external branchial appendages. Conus arteriosus with transverse series of valves. Ovaries transversely lamellated.[39]

Fig. 139.—Ceratodus miolepis.

Two species, C. forsteri and C. miolepis, are known from fresh waters of Queensland. The specimens hitherto obtained have come from the Burnett, Dawson, and Mary rivers, some from the fresh waters of the upper parts, others from the lower brackish portions. The fish is said to attain to a weight of twenty pounds and to a length of 6 feet. Locally, the settlers call it “Flat-head,” “Burnett- or Dawson-Salmon,” and the aborigines “Barramunda,” a name which they appear to apply also to other large-scaled freshwater fishes, as the Osteoglossum leichardti. In the stomach there is generally found an enormous quantity of the leaves of plants growing on the banks of rivers, evidently eaten after they had fallen into the water and when in a decomposing condition. The flesh of the fish is salmon-coloured, and much esteemed as food.

The Barramunda is said to be in the habit of going on land, or at least on mud-flats; and this assertion appears to be borne out by the fact that it is provided with a lung. However, it is much more probable that it rises now and then to the surface of the water in order to fill its lung with air, and then descends again until the air is so much deoxygenised as to render a renewal of it necessary. It is also said to make a grunting noise, which may be heard at night for some distance. This noise is probably produced by the passage of the air through the œsophagus when it is expelled for the purpose of renewal. As the Barramunda has perfectly developed gills, beside the lung, we can hardly doubt that, when it is in water of normal composition, and sufficiently pure to yield the necessary supply of oxygen, these organs are sufficient for the purpose of breathing, and that the respiratory function rests with them alone. But when the fish is compelled to sojourn in thick muddy water charged with gases, which are the products of decomposing organic matter (and this must be the case very frequently during the droughts which annually exhaust the creeks of tropical Australia), it commences to breathe air with its lung in the way indicated above. If the medium in which it happens to be is perfectly unfit for breathing the gills cease to have any function; if only in a less degree the gills may still continue to assist in respiration. The Barramunda, in fact, can breathe by either gills or lungs alone, or by both simultaneously. It is not probable that it lives freely out of the water, its limbs being much too flexible for supporting the heavy and unwieldy body, and too feeble generally to be of much use in locomotion on land. However, it is quite possible that it is occasionally compelled to leave the water, although we cannot believe that it can exist without it in a lively condition for any length of time.

Of its propagation or development we know nothing, except that it deposits a great number of eggs of the size of those of a newt, and enveloped in a gelatinous case. We may infer that the young are provided with external gills, as in Protopterus and Polypterus.

Fig. 140.—Tooth of fossil Ceratodus from Aust., near Bristol, natural size.

The discovery of Ceratodus does not date farther back than the year 1870, and proved to be of the greatest interest, not only on account of the relation of this creature to the other living Dipnoi and Ganoidei, but also because it threw fresh light on those singular fossil teeth which are found in strata of Triassic and Jurassic formations in various parts of Europe, India, and America. These teeth, of which there is a great variety with regard to general shape and size, are sometimes two inches long, much longer than broad, depressed, with a flat or slightly undulated, always punctated crown, with one margin convex, and with from three to seven prongs projecting on the opposite margin.

Fig. 141.—Dipterus macrolepidotus.

Second Family—Ctenododipteridæ.

Caudal fin heterocercal. Gular plates. Scales cycloid. Two pairs of molars and one pair of vomerine teeth.

Extinct. Dipterus (Ctenodus), Heliodus from Devonian strata.

Third Family—Phaneropleuridæ.

Caudal fin diphycercal; vertical fin continuous. Gular plates. Scales cycloid. Jaws with a series of minute conical teeth on the margin.

Extinct. Phaneropleuron from Devonian formations, and the carboniferous Uronemus are probably generically identical.

FOURTH SUB-ORDER—CHONDROSTEI.

Skeleton notochordal; skull cartilaginous, with dermal ossifications; branchiostegals few in number or absent. Teeth minute or absent. Integuments naked or with bucklers. Caudal fin heterocercal, with fulcra. Nostrils double, in front of the eyes.

First Family—Acipenseridæ.

Body elongate, sub-cylindrical, with five rows of osseous bucklers. Snout produced, subspatulate or conical, with the mouth at its lower surface, small, transverse, protractile, toothless. Four barbels in a transverse series on the lower side of the snout. Vertical fins with a single series of fulcra in front. Dorsal and anal fins approximate to the caudal. Gill-membranes confluent at the throat and attached to the isthmus. Branchiostegals none. Gills four; two accessory gills. Air-bladder large, simple, communicating with the dorsal wall of the œsophagus.

Fig. 142.—Tail of Acipenser. a, Fulcra; b, osseous bucklers.

Sturgeons are, perhaps, the geologically youngest Ganoids, evidence of their existence not having been met with hitherto in formations of older date than the Eocene clay of Sheppey. They are exclusively inhabitants of the temperate zone of the Northern Hemisphere, being either entirely confined to fresh water, or passing, for the purpose of spawning, a part of the year in rivers. They grow to a large size, and are the largest fishes of the fresh waters of the Northern Hemisphere, specimens 10 feet long being of common occurrence. The ova are very small, and so numerous that one female has been calculated to produce about three millions at one season; therefore their propagation, as well as their growth, must be very rapid; and although in many rivers their number is annually considerably thinned by the systematic manner in which they are caught when they ascend the rivers in shoals from the sea, no diminution has been observed. Wherever they occur they prove to be most valuable on account of their wholesome flesh. In Russia, besides, two not unimportant articles of trade are obtained from them, viz. Caviare, which is prepared from their ovaries, and Isinglass, which is made from the inner coats of their air-bladder. True Sturgeons are divided into two genera, Acipenser and Scaphirhynchus.

Acipenser.—The rows of osseous bucklers are not confluent on the tail. Spiracles present. Caudal rays surrounding the extremity of the tail.

About twenty different species of Sturgeons may be distinguished from European, Asiatic, and American rivers. The best known are the Sterlet (A. ruthenus) from Russian rivers, celebrated for the excellency of its flesh, but rarely exceeding a length of three feet; the Californian Short-snouted Sturgeon (A. brachyrhynchus); the Hausen (A. huso), from rivers, falling into the Black Sea and the Sea of Azow (rare in Mediterranean), sometimes 12 feet long, and yielding an inferior kind of isinglass; the Chinese Sturgeon (A. sinensis); the Common Sturgeon of the United States (A. maculosus), which sometimes crosses the Atlantic to the coasts of Great Britain; Güldenstædt’s Sturgeon (A. güldenstædtii), common in European and Asiatic rivers, which yields more than one-fourth of the caviare and isinglass exported from Russia; the Common Sturgeon of Western Europe (A. sturio), which attains to a length of 18 feet, and has established itself also on the coasts of Eastern North America.

Scaphirhynchus.—Snout spatulate; posterior part of the tail attenuated and depressed, so that it is entirely enveloped by the osseous scutes. Spiracles none. The caudal rays do not extend to the extremity of the tail, which terminates in a filament.

Four species are known: one (S. platyrhynchus) from the river-system of the Mississippi, and the three others from Central Asia; all are exclusively freshwater fishes; their occurrence in so widely distant rivers is one of the most striking instances by which the close affinity of the North American and North Asiatic faunas is proved.

Second Family—Polyodontidæ.

Body naked, or with minute stellate ossifications. Mouth lateral, very wide, with minute teeth in both jaws. Barbels none. Caudal fin with fulcra. Dorsal and anal fins approximate to the caudal. Four gills and a half; no opercular gill or pseudobranchia.