fig354

Fig. 354.—Pond Loach (Misgurnus fossilis), with lower view of mouth. ⅓ natural size.

The Loaches, Cobitidinae, which form a very natural sub-family, are small fishes, few species growing to a foot in length, mostly living in small streams and ponds. Many delight in the mud at the bottom, in which they move like Eels. In some cases, the branchial respiration appears to be insufficient, and the intestinal tract acts as an accessory breathing organ. The air-bladder, which is partially encased in a bony capsule, may be so reduced as to lose its hydrostatic functions and becomes transformed into a sensory organ, its outer exposed surface being connected with the skin by a meatus between the bands of muscle, and conveying the thermo-barometrical impressions to the auditory nerves; hence the name of "Wetterfisch," by which Loaches are known in some parts of Germany.

The Homalopterinae are more or less perfectly adapted to life in rapid streams, the most remarkable in this respect being Gastromyzon of North Borneo, in which the pectoral and ventral fins are much expanded to form, with the belly, a sucker by which the fish adhere to the stones of mountain torrents, showing a remarkable analogy to Exostoma among the Silurids.[666]

fig355

Fig. 355.Gastromyzon borneensis, ventral view, natural size.

Fam. 4. Siluridae.—Mouth non-protractile, bordered by the praemaxillaries and the maxillaries, or by the praemaxillaries only, the maxillaries being often rudimentary and supporting the base of a barbel; jaws usually toothed. Parietal bones usually confluent with the supraoccipital, forming a single large plate (parieto-occipital); symplectic and suboperculum absent. Pharyngeal bones normal, with small teeth. Ribs attached to the lower surface of long parapophyses; epipleurals absent. Pectoral fins inserted very low down, folding like the ventrals, often armed, like the dorsal, with a strong bony spine. Body naked or with bony plates. An adipose dorsal fin often present. One to four pairs of barbels.

The skull and the opercular apparatus show a reduction in the number of elements as compared with the Characinids and Cyprinids, such as the absence of the metapterygoid, the often rudimentary, rod-like condition of the palatine, and the fusion of the parietals with the supraoccipital.[667] The scapular arch is solidly united to the skull and is often very massive, and the occiput may be connected with the base of the dorsal fin by a buckler formed by the expansion of the first and second inter-neural bones. The pterygials or supports of the pectoral rays are large and reduced to two or three.[668] Teeth are rarely present on the maxillary bones (Diplomystes, Eutropiichthys), being usually confined to the praemaxillaries and dentaries; they often occur on the palate. The branchiostegal rays vary from 4 to 17. The lips are sometimes much developed, and may form a sucking disk, as in Euchilichthys and Exostoma. As in the Cyprinids, the pungent spines which may arm the fins have nothing in common with the true spines of Acanthopterygians; they result from the co-ossification, with age, of successive articles; but, contrary to the condition in the Cyprinids, the axis of the spine is single, not double. The ventral rays vary from 6 to 16, 6 being the most frequent number. Some of the exterior vertebrae may be solidly fused together, and also with the occipito-nuchal buckler. Prof. Ramsay Wright[669] has shown, by a study of the development, that the complex which follows the first vertebra, which is more or less rudimentary, if distinct, represents the fusion of the 2nd, 3rd, and 4th vertebrae, without even nerve-foramina denoting its compound origin; the first, strongly developed, transverse process represents that of the 4th vertebra. The air-bladder is usually large and trilocular, but additional septa may greatly complicate its structure, and external diverticula may also exist;[670] it may be more or less reduced and entirely or partially enclosed in a bilateral bony capsule formed by the transverse processes of the vertebrae, and sometimes (Nematogenys) ankylosed to the skull. In a few genera, like Cetopsis, the air-bladder seems to be altogether absent: it is reduced to two small oval sacs encased in the large compound anterior vertebra. As in Loaches, the air-bladder is often in immediate contact with the skin behind the shoulder-girdle. The intestinal tract may be simple and short (carnivorous forms) or extremely long and convoluted (Callichthys); as in Cyprinids, pyloric appendages are absent.

Cat-Fishes, as Silurids are usually called, are a large family embracing some 1000 species, spread over the fresh waters of all parts of the world, but mostly from between the tropics.[671] Only a few are marine (Plotosus, Arius, Galeichthys).

This family may be divided into eight subfamilies

(i.) Clariinae.—Dorsal and anal fins very long, extending to the caudal; gill-membranes free, or narrowly united to the isthmus. Asiatic-African genera: Clarias, Heterobranchus, Plotosus. Asiatic-Australian: Copidoglanis. Asiatic: Cranoglanis. African: Clariallabes, Allabenchelys, Gymnallabes, Channalabes. Australian: Cnidoglanis.

(ii.) Silurinae.—Dorsal fin very short or absent, anal very long; gill-membranes free. Europaeo-Asiatic: Silurus. Asiatic: Silurodon, Silurichthys, Saccobranchus, Wallago, Belodontichthys, Cryptopterus, Callichrous, Hemisilurus, Ailiichthys, Ailia, Schilbichthys, Laïs, Pseudeutropius, Pangasius, Osteogeniosus, Helicophagus, Silondia. African: Eutropius, Schilbe, Siluranodon, Physailia, Parailia. Australian: Eumeda, Neosilurus.

(iii.) Bagrinae.—Dorsal fin short, followed by a more or less elongate adipose fin; anal short or moderate; gill-membranes free. Asia, Africa, America, Australia: Arius. Asia and America: Amiurus. Asiatic: Macrones, Pseudobagrus, Liocassis, Bagroides, Bagrichthys, Rita, Acrochordonichthys, Acysis, Olyra, Hemipimelodus. African: Bagrus, Clarotes, Chrysichthys, Gephyroglanis, Auchenoglanis, Notoglanidium, Anoplopterus, Galeichthys. American: Diplomystes, Paradiplomystes, Aelurichthys, Genidens, Noturus, Callophysus, Pimelodus, Pimelodina, Nanoglanis, Heptapterus, Nematogenys, Pariolius, Pirinampus, Conorhynchus, Notoglanis, Callophysus, Sorubim, Piramutana, Bagropsis, Sciades. Australian: Nedystoma, Pachyula.

(iv.) Doradinae.—A short-rayed dorsal fin and an adipose, the latter sometimes replaced by a second rayed dorsal; anal short or moderate; gill-clefts more or less widely interrupted below. African: Synodontis, Chiloglanis, Atopochilus, Euchilichthys, Mochocus, Doumea, Phractura, Paraphractura, Andersonia, Trachyglanis, Belonoglanis. Asiatic: Bagarius, Glyptosternum, Gagata, Pseudecheneis, Exostoma, Sisor, Breitensteinia, Sosia, Chaca. South American: Doras, Oxydoras, Leptodoras, Physopyxis, Glanidium, Centromochlus, Wertheimeria, Cetopsis.

(v.) Malopterurinae.—No rayed dorsal fin, an adipose; anal short; gill-clefts interrupted below. African: Malopterurus.

(vi.) Callichthyinae.—Dorsal, anal, and adipose fins short; body completely cuirassed; praemaxillaries much reduced, the border of the upper jaw formed mainly by the maxillaries. South American: Callichthys, Corydoras.

(vii.) Hypophthalminae.—Dorsal fin short, behind the ventrals, anal long; gill-clefts wide or interrupted below. South American: Ageniosus, Trachelyopterus, Auchenipterus, Epapterus, Tetranematichthys, Hypophthalmus, Helogenes.

(viii.) Trichomycterinae.—Dorsal fin short, far back, behind the ventrals; no adipose fin; anal short; operculum and interoperculum armed with erectile spines. South American: Trichomycterus, Eremophilus, Stegophilus, Vandellia, Acanthopoma.

Our knowledge of the distribution in time of the Silurids is still very scanty, and throws no light on the derivation of the group. Arius, and two genera apparently related to it, Rhineaster and Bucklandium, have left remains in the Eocene of Europe and North America, and traces of various recent genera have been found in later Tertiary deposits in Europe, Asia, and North and South America.

The habits of the Silurids are extremely diversified, and the shape of the body varies accordingly. The body may be very short and the head enormous and excessively depressed, for instance in the Indo-Burmese Chaca lophioides, which, as its name implies, resembles the Fishing-Frog or Angler; stout and Cottus-like in some South American Pimelodus; Loach-like in Trichomycterus and Stegophilus; more or less Eel-shaped in Clarias and its allies, etc.; the extreme of slenderness obtains in the African Channalabes, the body being excessively elongate (over 100 vertebrae), the ventral fins absent, and the pectorals rudimentary or absent. Among other remarkable forms may be mentioned the Indian Sisor, which resembles Aspredo, and in which the upper caudal ray is much thickened and greatly prolonged; Pseudecheneis, living in rapids of the Himalayas and Khasia hills, provided with a transversely plaited ventral disk between the pectoral fins; the African Phractura and Andersonia, resembling Loricaria; and the likewise African Belonoglanis, comparable to a Needle-Fish. The spines which so frequently arm the dorsal and pectoral fins may be barbed or serrated, and constitute formidable defensive weapons; in the South American Ageniosus valenciennesi, the maxillary bone is transformed into a strong, barbed, erectile spine, replacing the barbel. Stings of even the smaller Cat-Fish are at least as painful as that of a bee, and this is probably due to some poisonous property of the dermal secretion of the Fish.

fig356

Fig. 356.—Harmout, Clarias anguillaris (after Valenciennes). ¼ nat. size.

Cope believed an orifice at or above the axil of the pectoral fin in Noturus to be the opening of the duct of a poison-gland; "from it may frequently be drawn a solid gelatinous style ending in a tripod, each limb of which is dichotomously divided into short branches of regular length." I think this condition of things has nothing to do with a poison-organ, and is merely a repetition of what is observed in Loaches and in the Characinid Xenocharax, where I have found a gelatinous substance filling the short duct by which the membrane of the air-bladder is placed in communication with the skin and the sensory organ of the lateral line. Most Silurids can live in very foul water, taking in air from the surface, and spend a comparatively long time out of the water, without being possessed of any special apparatus for atmospheric respiration. A few genera, however, are provided with an accessory breathing organ: in Clarias, Heterobranchus, and allies, there is a dendritic superbranchial organ, in Saccobranchus a long air-sac, extending from the first branchial cleft along the side of the body, as described above, p. 295; and these Fish can live for days on land. Clarias lazera has been observed, in Senegambia, to spend several months of the dry season in burrows, from which it emerges at night to crawl about in search of food. Many Silurids, but especially Doras and Synodontis, are known to produce sounds in and out of the water by means of a special mechanism of the air-bladder and the processes of the vertebrae above it, combined with the movements of the pectoral spine grinding in the glenoid cavity.[672] In South America, Doras has been observed to move rapidly on land, projecting itself forward on the pectoral spines by the elastic spring of the tail, travelling long journeys over land, from one drying pond to another, spending whole nights on the way; these migrations sometimes take place in numerous bands, baskets of the small Fish being filled by the Indians who come across them.[673] The African Synodontis are much in the habit of floating or swimming leisurely on the surface with the belly in the air, as was well known to the ancient Egyptians, who have frequently depicted the Fish in this anomalous position. A curious fact in connexion with this habit is that S. membranaceus and S. batensoda, in which it has most frequently been observed, show an inversion of the ordinary mode of coloration, the lower parts being dark brown or black and the upper pale silvery grey. The electric Cat-Fish (Malopterurus electricus), is also a native of Africa, occurring all over the tropical parts of that continent and also in the Lower Nile, growing to a length of three feet. Its flesh is more esteemed than that of other Silurids. It avoids light and is slow in its movements. The electrical apparatus differs absolutely from that of all other Fishes, being derived from the integument, belonging to the glandular system, and surrounding the whole body with a thick coat of grease or gelatinous substance; the apparatus is governed by a single nerve on each side proceeding from a huge ganglionic cell at the anterior extremity of the spinal cord.[674] The shocks given by Madopterurus are very powerful, and the Fish is called "Raad" by the Arabs, a name which means "thunder." Kept in an aquarium with other Fishes, even of the same species, the "Raad" soon kills its companions.

fig357

Fig. 357.Synodontis decorus, from the Congo. ⅓ nat. size.

fig358

Fig. 358.Callichthys littoralis, from South America. ⅔ nat. size.

In this family the eggs and young are usually looked after by the parents. Aristotle observed that the male of the European Silurus glanis watches over and defends the eggs. In one of the commonest North American Cat-Fishes, Amiurus nebulosus, a species which has been largely introduced into some parts of Europe of late, now thriving in many ponds and more or less polluted streams of the Continent, the eggs are deposited near the banks of weedy ponds and rivers without currents, in concealed places beneath logs, stumps, or even in pails or other receptacles, failing which both parents join in excavating a sort of nest in the mud, a work often requiring two or three days of incessant labour. The male watches over the eggs, and later leads the young in great schools near the shore, seemingly caring for them as the hen for her chickens.[675] The Doras and the Callichthys of South America, according to Hancock[676] and Vipan,[677] build regular nests of grass or leaves, sometimes placed in a hole scooped out in the bank, in which they cover their eggs and defend them, male and female sharing in this parental duty. In the likewise South American Corydoras (Callichthys paleatus), as observed by Carbonnier,[678] a lengthy courtship takes place, followed by an embrace, during which the female receives the seminal fluid in a sort of pouch formed by the folded membranes of her ventral fins; immediately after, five or six eggs are produced and received in the pouch, to be afterwards carefully placed in a secluded spot. This operation is repeated many times, until the total number of eggs, about 250, have been deposited. In accordance with these pairing habits, the pectoral spines of the male, which are used in amplexation, are longer and stronger than those of the female. These Fish are monogamous, and both parents remain by the side of the nest, furiously attacking any assailant. Dr. R. Semon[679] has made observations in Queensland on the habits of Arius australis, which builds nests in the sandy bed of the Burnett River. These nests consist of circular basin-like excavations, about 20 inches in diameter, at the bottom of which the eggs are laid, and covered over by several layers of large stones. A still more efficient protection is afforded their progeny by the marine and estuarine species of Arius,[680] Galeichthys,[681] and Osteogeniosus,[682] the male, more rarely the female, carrying the eggs in the mouth and pharynx; these eggs, few in number, are remarkably large, measuring as much as 17 or 18 millimetres in diameter in Arius commersonii, a Fish of three or four feet in length. According to Babuchin, Malopterurus also is said by the Nile fishermen to shelter its fry in the mouth.

Some of the Silurids attain to a very large size. Among these is the type of the family, Silurus glanis, the "Wels" of the Germans, its only European representative, which occurs over a great part of Europe, but is absent from the British Isles, France, the Spanish Peninsula, and Italy. It is most abundant in the Danube basin, where it sometimes reaches a length of 10 feet or more and a weight of 400 lbs. It is the largest strictly fresh-water Fish of Europe. Among the smallest species, we have to mention the "Candiru" of Brazil, Vandellia cirrhosa, 60 millimetres in length and 3 or 4 in diameter, which is believed to enter and ascend the urethra of people bathing, being attracted by the urine; the Fish, having once made its way into the urethra, cannot be pulled out again, owing to the erectile spines which arm its gill-covers. The natives of some parts of the Amazons are in great dread of this Fish, and protect themselves when entering the water by wearing a sheath formed of a small, minutely-perforated cocoanut-shell suspended from a belt of palm-fibres.[683] According to Reinhardt[684] the allied Stegophilus insidiosus, a small colourless Fish, 30 to 40 mm. long, from Brazil and Argentine, lives parasitically in the gill-cavity of large Cat-Fishes (Platystoma). Dr. F. Silvestri has noticed that it sucks the blood in the gills of Platystoma coruscans, a Silurid growing to a length of 6 feet.

fig359

Fig. 359.—Upper view of heads of Chaetostomus cirrhosus, male and female. (Nat. size.)

Fam. 5. Loricariidae.—Distinguished from the preceding by the sessile ribs and the absence of the transverse processes in the praecaudal vertebrae, which have bifid neural spines. The air-bladder is always much reduced, and enclosed in a right and a left bony capsule formed by the skull and the anterior vertebrae. Gill-openings narrow clefts. The mouth is inferior, with more or less developed circular lips and feeble dentition; it is used as a sucker, by which the Fish fixes itself to any hard object with such strength that it cannot be pulled off without great difficulty. The teeth are usually slender and bicuspid. The food consists of very small prey and more or less putrefied organic substances, the intestine being usually extremely elongate and much convoluted. The habits of these Fish are very little known, but the fact that the males of many species have the pectoral fins much stronger than the females renders it probable that they pair like Callichthys. There are other sexual differences in many species of Plecostomus, Chaetostomus, and Loricaria, as the presence of dermal tentacles on the snout (see Fig. 359), or of hair-like bristles on various parts of the head and fins in the males, which are usually of larger size.

About 200 species are known, all from the tropical and subtropical parts of Central and South America. The largest species (Chaetostomus gigas) measures 2½ feet; many are of very small size.[685] The genera may be referred to two sub-families:—

(i.) Arginae.—Body naked; ribs strong. Arges, Stygogenes, Astroblepus.

(ii.) Loricariinae.—Body cuirassed by bony plates; ribs very slender. Plecostomus, Liposarcus, Chaetostomus, Cochliodon, Pterygoplichthys, Rhinelepis, Acanthicus, Otocinclus, Hypoptopoma, Loricaria, Acestra.

fig360

Fig. 360.Acestra gladius, from the Jurua River, with upper and lower views of head and trunk. (⅔ nat. size.)

The "Prenadillas" of the Andes, Arges and Stygogenes, were believed to live in subterranean waters within the bowels of active volcanoes, and to be ejected with streams of mud and water during eruptions, a story that has been repeated by Humboldt. The fact is that they live in small torrents at great altitudes (up to 10,700 feet), and are swept down during periods of disturbance caused by the eruption of the volcano.[686] The members of the sub-family Loricariinae vary much in the shape of the body, which may be short and stout, or more or less slender, the extreme in the latter respect being attained by the species of the genus Acestra.

Fam. 6. Aspredinidae.—This family is also closely related to the Siluridae. The ribs are sessile as in the Loricariidae, but inserted very low down on the centra, which higher up bear strong transverse processes. The opercular bone is entirely absent. The gill-opening is reduced to a foramen in front of the pectoral fin. The head is extremely depressed and the mouth terminal; the tail is very slender; the body is naked. The air-bladder is large and free, the intestinal canal short. Four genera from South America: Aspredo, Bunocephalus, Bunocephalichthys, Dysichthys. Species 18. Aspredo, of the Guianas, the largest form, reaching to about a foot in length, is remarkable for the manner in which the female carries her eggs. The skin of the lower parts assumes a spongy condition about the breeding season, and the eggs, after being deposited, become attached to the lower surface of the head, belly, and paired fins, forming a single layer; each egg becomes connected with the skin of the mother by a cup-shaped, pedunculate base, supplied with blood-vessels and coated with a layer of epithelium, the formation of which is still unexplained.[687]

CHAPTER XXII

TELEOSTEI (CONTINUED): SYMBRANCHII—APODES—HAPLOMI—HETEROMI—CATOSTEOMI—PERCESOCES—ANACANTHINI

Sub-Order 3. Symbranchii

Eel-shaped Fishes without paired fins, with the pectoral arch free or suspended from the skull, and with the anterior vertebrae distinct, without Weberian ossicles. Gill-openings confluent into a single, ventral slit. Air-bladder absent.

The structure of the skull conforms to that of typical Malacopterygians. The praemaxillary and maxillary are well developed, the latter placed behind the former, and forming but a very small part of the oral border; the symplectic is present; the parietals form a long sagittal suture, and separate the frontals from the supraoccipital. The vertebrae are very numerous, the praecaudal bearing very strong parapophyses, to which short, slender ribs are attached. The skin is naked (Symbranchidae) or covered with minute scales (Amphipnoidae), and the vertical fins are rudimentary, reduced to mere dermal folds.

Like the Apodes, which they resemble in general appearance, these Fishes are no doubt derived from some low type with abdominal ventral fins, but whether from the Malacopterygii or the Haplomi we have as yet no data from which to conclude. Only two families are known.

Fam. 1. Symbranchidae.—Post-temporal well developed, forked, attached to the skull. Inhabitants of the fresh or brackish waters of South-Eastern Asia, Tropical America, Australia, and Tasmania. Three genera are known: Symbranchus, with two species from India and the Malay region, and one from Central and South America; Monopterus, with a single species from China, Japan, and the Malay region; and Chilobranchus, with two species from Australia and Tasmania. Although the South American Symbranchus has been observed to live in marshes which periodically dry up, the Fish burying itself in the mud like a Lepidosiren, the branchiae are fully developed on the four branchial arches. In Monopterus, of similar habits, the branchial laminae are rudimentary, and on three arches only. No accessory breathing organ is known to exist.

fig361

Fig. 361.Monopterus javanensis. Lower view of head, showing gill-opening (go): lower view of middle praecaudal vertebrae: and side view of skull and pectoral arch. ar, Articular; br, branchiostegal rays; bra, branchial arches; cl, clavicle; d, dentary; eot, epiotic; eth, ethmoid; f, frontal; hm, hyomandibular; iop, interoperculum; m, maxilla; mpt, metapterygoid; n, nasal; op, operculum; p, parietal; pm, praemaxilla; pop, praeoperculum; ppt, pterygopalatine; ptte, post-temporal; q, quadrate; scl, supra-clavicle; so, supra-occipital; sop, suboperculum; sq, squamosal; sy, symplectic.

Fam. 2. Amphipnoidae.—Post-temporal absent, the shoulder-girdle free from the skull. The Cuchia, Amphipnous cuchia, the sole representative of this family, an inhabitant of the fresh and brackish waters of India and Burma, growing to two feet in length, is remarkable for the presence of a respiratory air-sac on each side of the neck behind the head, communicating with the gill-cavity. Of the three branchial arches the second alone possesses gill-filaments; the third supports, in their place, a thick and semi-transparent tissue; the principal organs of respiration are two small bladders, resembling the posterior portions of the lungs of snakes, which the animal has the power of filling with air immediately derived from the atmosphere. Although covered over by the common integuments, these bladders present externally, when inflated, two protuberances of a round shape. Of the whole volume of blood contained in the branchial artery, one-third passes through the gills and respiratory bladders, whilst the other two-thirds are conveyed directly from the heart to the aorta without being exposed to the action of the air.[688] This amphibious Fish, when in the water, constantly rises to the surface for the purpose of respiration, and it is often found lying in the grassy sides of ponds after the manner of Snakes.

Sub-Order 4. Apodes.

Air-bladder, if present, communicating with the digestive tract by a duct. Praemaxillaries absent; the maxillaries, if present, separated on the median line by the coalesced ethmoid and vomer. Pectoral arch, if present, not connected with and remote from the skull; mesocoracoid arch absent. Fins without spines, the ventrals absent. Anterior vertebrae distinct, without Weberian ossicles.

The Apodes or Eels are elongate, serpentiform Fishes with naked skin, or with minute scales imbedded in the skin, the opercular bones small and completely hidden under the integument; narrow or minute gill-openings; the vertical fins, if present, confluent behind or separated by the projecting tip of the tail. The pterygo-palatine arch is often reduced or absent, and there is no distinct symplectic; the supraoccipital bone is small, separated from the frontals by the parietals, which meet on the middle line. The vertebrae are very numerous (up to 225), and the praecaudals bear strong parapophyses, to which short, slender ribs may be attached; epineurals are sometimes present. The five families into which this sub-order is divided show remarkable degrees of simplification of the skull, through reduction or loss of either the maxillary or the pterygo-palatine arches.

There has been much difference of opinion in the determination of the bones of the upper jaw in these Fishes. Cuvier regarded the lateral bones of the upper jaw as praemaxillaries, Owen and Richardson as palatines (at least in Muraenas), whilst Peters and most recent authors have identified them throughout the order as maxillaries.[689] The conclusion I have come to from the examination of numerous skulls belonging to various genera, is that the praemaxillaries have disappeared in all, whilst the maxillaries have persisted in the true Eels (Anguillidae) and disappeared in the Muraenidae, their place being taken by the fused palato-ectopterygoids, which may even join the mandibular suspensorium. The vestigial bone, regarded by Jacoby as the pterygoid in Muraena helena, may be identified as the meta-pterygoid, and therefore does not disprove the homology, here suggested, of the other elements of the palate.

Fam. 1. Anguillidae.—Maxillaries present, separated on the median line by the ethmo-vomer; palato-pterygoid bone present, connected with the hyomandibular and quadrate; gill-clefts separate, opening into the pharynx by wide slits; tongue present; vent far removed from the head.

fig362

Fig. 362.—Skull and pectoral arch of Conger vulgaris, side view. Ar, Articular; br, branchiostegal rays; ch, ceratohyal; cl, clavicle; cor, coracoid; d, dentary: eot, epiotic; eth, ethmoid; f, frontal; hm, hyomandibular; iop, interoperculum; m, maxilla; n, nasal; op, operculum; p, parietal; pop, praeoperculum; por, praeorbital; ppt, pterygo-palatine; ps, parasphenoid; ptf, post-frontal; ptr, pterygials; q, quadrate; sc, scapula; scl, supra-clavicle; so, supra-occipital; sop, suboperculum; sq, squamosal; uh, urohyal; v, vomer.

Spread over all the seas of the temperate and tropical zones, often descending to the greatest depths, a few entering fresh waters. Many are known to undergo very striking metamorphoses, the pellucid, strongly compressed larvae (Leptocephalus) having long been a puzzle to naturalists.

Nearly 150 recent species are known, of which some 50 are deep-sea forms, occurring down to 2500 fathoms. Scanty fossil remains, referable to recent genera or scarcely different from them, are known from the Eocene of Europe. The Cretaceous genus Urenchelys, from England and the Lebanon, is interesting as representing a more generalised type, the hindmost vertebrae bearing a pair of expanded hypural bones, showing the diphycercal Eels to have been derived from Fishes with a normal caudal fin.

The genera are numerous. The following are the principal:—Anguilla, Simenchelys, Ilyophis, Conger, Coloconger, Congromuraena, Uroconger, Heteroconger, Muraenesox, Nettastoma, Nettophichthys, Saurenchelys, Nettenchelys, Myrus, Myrophis, Derichthys, Chilorhinus, Muraenichthys, Liuranus, Ophichthys, Moringua.

In the first four genera, small, more or less lineal rudimentary scales are embedded in the skin, arranged in small groups, which are placed obliquely at right angles to one another, forming a curious pattern; but these scales are so small that they escape the notice of the superficial observer, hence Eels have been improperly included among the Fishes forbidden as food by the Mosaic prescriptions. In the other genera, including the exclusively marine Conger of our coasts, scales are really absent.

The Common Eel (Anguilla vulgaris) has a very wide distribution, being found over the greater part of Europe, North Africa, Temperate Asia, and perhaps also North America east of the Rocky Mountains, Mexico, and the West Indies. Its record from Australia and New Zealand is probably due to the imperfection of our knowledge of the specific characters. It is not found in the Black Sea nor in the rivers flowing into it, owing, no doubt, to the sulphurous nature of the bottom of the sea, to which, as we now know, these Fish would have to resort for breeding.

The mode of propagation of the Eel long remained a mystery, from the fact that individuals found in fresh water never show ripe genital glands. The idea had been entertained of their being hermaphrodite, and internal parasites had also given rise to the belief in their viviparous nature. The genital glands of the female were first investigated by Rathke in 1838, but it was not until 1874 that those of the male were discovered by Syrski, and shortly after fully described by L. Jacoby, who, in his final contribution to the subject, concluded that Eels need salt water for the development of their organs of generation, and that this development takes place, not near the coast, but further out in deep water.

fig363

Fig. 363.—Larva of Common Eel, Leptocephalus brevirostris of Kaup. (After Kaup.)

As a rule it is not until the fifth or sixth year that the Eels go to the sea for the purpose of propagation, which takes place at great depths—at least 200 fathoms. Males have been observed to precede the females. The breeding season over, the Eels do not return to fresh waters, but are believed to die soon after. The eggs were discovered by Raffaele in 1888 in the Gulf of Naples, and shortly after Grassi and Calandruccio finally settled the question of the breeding and development of the Fish from observations made in the Mediterranean. Their conclusions are thus summed up:—"The Common Eel matures in the depths of the sea, where it acquires larger eyes than are ever observed in individuals which have not yet migrated to deep water. The abysses of the sea are its spawning places; its eggs float in the sea water. In developing from the egg, it undergoes a metamorphosis, it passes through a larval form denominated Leptocephalus brevirostris." What length of time the development requires is not yet fully established, since the Leptocephali are rarely found at the surface, most of the specimens studied by Grassi and Calandruccio having been obtained from the stomach of the Sun-Fish (Orthagoriscus mola) in the Straits of Messina; but it is believed that the young Eels or "elvers," which ascend our rivers in such prodigious numbers in spring and summer ("Eel-Fares") are already one year old. Some individuals apparently spend their whole life in fresh waters, but they are barren.[690] A specimen was kept in confinement in the family of the French naturalist Desmarest for upwards of 40 years, growing to a length of 4½ feet, being already of large size at the time of its capture. Eels are extremely voracious, and endowed with an extraordinary tenacity of life; they can live for many hours out of the water, and are often met with at night creeping through the grass of meadows from one pond or stream to another.

One of the most remarkable among the deep-sea Eels is the Snub-nosed Eel (Simenchelys parasiticus), which has been found in great numbers off Newfoundland and the Azores, at depths of 200 to 900 fathoms. The maxillary and mandibular bones are very short and massive, provided with large obtuse teeth; the head is short and bulldog-like in aspect, the mouth small and bordered by a thick circular lip. Some specimens have been observed to burrow in the muscles of living Halibut and other large Fishes, after the manner of Myxine.

Fam. 2. Nemichthyidae.—Distinguished from the preceding by the position of the vent, which is close to, or at no great distance from, the gill-openings. The rays of the vertical fins are connected by thin membrane instead of being imbedded in thick skin, as in most Eels; in some of the genera the jaws are excessively prolonged, needle-like, sometimes recurved. Deep-sea Eels of small size, represented in the Atlantic, Pacific, and Indian Oceans by about 10 species, referred to 6 genera: Dysomma, Dysommatopsis, Nemichthys, Spinivomer, Serrivomer, Gavialiceps.

Fam. 3. Synaphobranchidae.—Maxillaries narrowly separated on the median line, their extremity strongly attached by ligament to the mandible; pterygo-palatine arch absent. Gill-openings externally confluent into a single ventral slit. Deep-sea Fishes, resembling the true Eels in the general form and in the presence of linear scales placed at right angles, but differing in the absence of the pterygo-palatine arch, as in the Saccopharyngidae. Eight species of Synaphobranchus are known, from the Atlantic, Pacific, and Indian Oceans, at depths of 200 to 2000 fathoms.

Fam. 4. Saccopharyngidae.—Maxillaries narrowly separated on the median line, extremely elongate; mouth enormous; pterygo-palatine arch absent; hyomandibular arch slender and movably articulated to the cranium, the two bones (hyomandibular and quadrate) of which it is composed being capable of being swung in all directions; branchial arches far behind the skull; no branchiostegal rays or pharyngeal bones.

Extraordinary-looking deep-sea Fishes allied to the Eels, of which they appear to be a further degraded type, the muscles being feebly developed and the skeleton imperfectly calcified. The mouth, furnished with rather long but feeble, or even minute teeth, and the pharynx and stomach are capable of great distension, these Fish being able to get outside a prey very much larger than themselves; the eyes are situated far forward on the head; the tail is extremely slender and elongate. Four genera are known, each with a single species, from the Atlantic: Saccopharynx, Eurypharynx, Macropharynx, and Gastrostomus. The depths at which they have been obtained vary between 389 and 1467 fathoms, but three out of the four known specimens of Saccopharynx were brought to the surface by having swallowed a Fish too large for the capacity of the stomach. The length of the largest specimen is about 6 feet, of which the tail constitutes nearly three-fourths.

fig364

Fig. 364.Saccopharynx ampullaceus, ⅓ nat. size. (After Günther.)