| Plectognathi | Anura | |||||||||
| │ | Lophobranchia | Peromela | │ | |||||||
| │ | │ | │ | │ | |||||||
| │ | │ | │ | Sozura | |||||||
| Labyrinthodonta | │ | │ | |||||||
| Stichobrancia Physoclisti | │ │ | │ │ | │ │ | |||||||
| Enchelygenes | │ |
| │ | |||||||
| │ │ | │ │ | Ganocephala Phractamphibia | Sozobranchia Lissamphibia | |||||||
| │ | │ | │ | │ | |||||||
|
| |||||||||
| │ | Amphibia | |||||||||
| Thrissogenes Physostomi Teleostei | Semæopteri | │ │ │ | ||||||||
| │ | Fulcrati | │ | Protopteri | │ | Plesiosauria | |||||
| Pycnoscolopes | │ | │ | │ | │ | Icthyosauria | │ | ||||
| │ | │ | │ | │ | │ | │ | │ | ||||
| Cœloscolopes Cycliferi Cycloganoides) |
Rhombiferi (Rhomboganoides) | │ │ │ │ | │ │ │ │ | │ │ │ │ | │ │ │ │ | |||||
| │ | │ | │ | │ | │ | │ | |||||
| Dipneusta | │ │ | │ │ | │ │ | ||||||
Sturiones │ │ | │ │ │ │ | │ │ │ │ | │ │ │ │ |
Halisauria | ||||||
| │ | │ | │ | │ | │ | ||||||
| Cephalaspidæ | │ | Rajacei | │ |
| ||||||
| │ | │ | Amphipneumona | |||||||
| Pamphracti Tabuliferi (Placoganoides) Ganoides | │ │ │ │ | │ │ │ │ | │ │ │ │ | |||||||
| │ │ | │ │ | Chimæracei Holocephali | │ │ | |||||||
| Squalacei | │ | │ | │ | |||||||
| │ | │ | │ | │ | |||||||
| │ │ | │ │ | ||||||||
| │ | │ | │ | ||||||||
| │ | │ | │ | ||||||||
Fish Amphirrhina | │ │ │ │ | |||||||||
| │ | ||||||||||
| │ │ | Cyclostoma Monorrhina | |||||||||
| ||||||||||
| Craniota | ||||||||||
Genuine fish are divided into three distinct sub-classes, namely, Primæval fish, Ganoid fish, and Osseous fish. The oldest of these, where the original form has been most faithfully preserved, is that of the Primæval fish (Selachii). Of these there still exist Sharks (Squali), and Rays (Rajæ), which are classed together as cross-mouthed fishes (Plagiostomi), and the strange and grotesquely formed Sea-cats, or Chimæracei (Holocephali). These primary fish of the present day, which are met with in all seas, are only poor remains of the prevailing animal groups, rich in forms, which the Selachii formed in the earlier periods of the earth’s history, and especially during the palæolithic period. Unfortunately all Primæval fish possess a cartilaginous, never a completely osseous skeleton, which is but little, if at all, capable of being petrified. The only hard parts of the body which could be preserved in a fossil state, are the teeth and fin-spikes. These are found in the older formations in such quantities, varieties, and sizes, that we may, with certainty, infer a very considerable development of Primæval fish in those remote ages. They are even found in the Silurian strata, which contain but few remains of other Vertebrata, such as Enamelled fish (and these only in the most recent part, that is, in the upper Silurian). By far the most important and interesting of the three orders of Primæval fish are Sharks; of all still living double-nostriled animals, they are probably most closely allied to the original primary form of the whole group, namely, to the Proselachii. Out of these Proselachii, which probably differed but little from genuine Sharks, Enamelled fish, and the present Primæval fish, in all probability, developed in one direction, and the Dipneusta, Sea-dragons, and Amphibia in another.
The Ganoid, or Enamelled fish (Ganoides), in regard to their anatomy stand midway between the Primæval and the Osseous fish. In many characteristics they agree with the former, and in many others with the latter. Hence, we infer that genealogically they form the transition from Primæval to Osseous fish. The Ganoids are for the most part extinct, and more nearly so than the Primæval fish, whereas they were developed in great force during the entire palæolithic and mesolithic periods. Ganoid fish are divided into three legions according to the form of their external covering, namely, Mailed, Angular-scaled, and Round-scaled. The Mailed Ganoid fish (Tabuliferi) are the oldest, and are directly allied to the Selachii, out of which they originated. Fossil remains of them, though rare, are found even in the upper Silurian (Pteraspis ludensis of the Ludlow strata). Gigantic species of them, coated with strong bony plates, are found in the Devonian system. But of this legion there now lives only the small order of Sturgeons (Sturiones), including the Spade-sturgeons (Spatularidæ), and those Sturgeons (Accipenseridæ) to which belong, among others, the Huso, which yields isinglass, or sturgeon’s sound, and the Caviar-sturgeon, whose eggs we eat in the shape of caviar, etc. Out of the mailed Ganoid fish, the angular and round-scaled ones probably developed as two diverging branches. The Angular-scaled Ganoid fish (Rhombiferi)—which can be distinguished at first sight from all other fish by their square or rhombic scales—are at present represented only by a few survivors, namely, the Finny Pike (Polypterus) in African rivers (especially the Nile), and by the Bony Pike (Lepidosteus) in American rivers. Yet during the palæolithic and the first half of the mesolithic epochs this legion formed the most numerous group of fishes. The third legion, that of Round-scaled Ganoid fish (Cycliferi), was no less rich in forms, and lived principally during the Devonian and Coal periods. This legion, of which the Bald Pike (Amia), in North American rivers, is the only survivor, was especially important, inasmuch as the third sub-class of fish, namely, Osseous fish, developed out of it.
Osseous fish (Teleostei) include the greater portion of the fish of the present day. Among these are by far the greater portion of marine fish, and all of our fresh-water fish except the Ganoid fish just mentioned. This class is distinctly proved by numerous fossils to have arisen about the middle of the Mesolithic epoch out of Ganoid fish, and moreover out of the Round-scaled, or Cycliferi. The Thrissopidæ of the Oolitic period (Thrissops, Leptolepis, Tharsis), which are most closely allied to the herrings of the present day, are probably the oldest of all Osseous fish, and have directly arisen out of Round-scaled Ganoid fish, closely allied to the existing Amia. In the older Osseous fish of the legion called Physostomi, as also in the Ganoides, the swimming bladder throughout life was connected with the throat by a permanent air passage (a kind of windpipe). This is still the case with all the fish belonging to this legion, namely, with herrings, salmon, carp, shad, eels, etc. However, during the chalk period this air passage, in some of the Physostomi, became constricted and closed, and the swimming bladder was thus completely separated from the throat. Hence there arose a second legion of Osseous fish, the Physoclisti, which did not attain their actual development until the tertiary epoch, and soon far surpassed the Physostomi in variety. To this legion belong most of the sea fish of the present day, especially the large families of the Turbot, Tunny, Wrasse, Crowfish, etc., further, the Lock-jaws (Plectognathi), Trunk fish, and Globe-fish and the Bushy-gills (Lophobranchi), viz., Pipe-fish, and Sea-horses. There are, however, only very few Physoclisti among our river fish, for instance, Perch and Sticklebacks; the majority of river fish are Physostomi.
Midway between genuine Fish and Amphibia is the remarkable class of Mud-fish, or Scaly Sirens (Dipneusta, or Protopteri). There now exist only a few representatives of this class, namely, the American Mud-fish (Lepidosiren paradoxa) in the region of the river Amazon, and the African Mud-fish (Protopterus annectens) in different parts of Africa. A third large Salamander-fish (Ceratodus Fosteri) has lately been discovered in Australia. During the dry season, that is in summer, these strange animals bury themselves in a nest of leaves in the dry mud, and then breathe air through lungs like the Amphibia. But during the wet season, in winter, they live in rivers and bogs, and breathe water through gills like fish. Externally, they resemble fish of the eel kind, and are like them covered with scales; in many other characteristics also—in their internal structure, their skeleton, extremities, etc.—they resemble Fish more than Amphibia. But in certain features they resemble the Amphibia, especially in the formation of their lungs, nose, and heart. There is consequently an endless dispute among zoologists, as to whether the Mud-fish are genuine Fish or Amphibia. Distinguished zoologists have expressed themselves in favour of both opinions. But in fact, owing to the complete blending of characteristics which they present, they belong neither to the one nor to the other class, and are probably most correctly dealt with as a special class of Vertebrata, forming the transition between Fishes and Amphibians. The still living Dipneusta are probably the last surviving remains of a group which was formerly rich in forms, but has left no fossil traces on account of the want of a solid skeleton. In this respect, these animals are exactly like the Monorrhina and the Leptocardia. However, teeth are found in the Trias which resemble those of the living Ceratodus. Possibly the extinct Dipneusta of the palæolithic period, which developed in the Devonian epoch out of primæval fish, must be looked upon as the primary forms of the Amphibia, and thus also of all higher Vertebrata. At all events the unknown forms of transition—from Primæval fish to Amphibia—were probably very like the Dipneusta.
A very peculiar class of Vertebrate animals, long since extinct, and which appears to have lived only during the secondary epoch, is formed by the remarkable Sea-dragons (Halisauria, or Enaliosauria, also called Nexipoda, or Swimming-footed animals). These formidable animals of prey inhabited the mesolithic oceans in great numbers, and were of most peculiar forms, sometimes from thirty to forty feet in length. From many and excellently preserved fossil remains and impressions, both of the entire body of Sea-dragons as well as of single parts, we have become very accurately acquainted with the structure of their bodies. They are usually classed among Reptiles, whilst some anatomists have placed them in a much lower rank, as directly allied to Fish. Gegenbaur’s recently published investigations, which place the structure of their limbs in a true light, have led to the surprising conclusion that the Sea-dragons form quite an isolated group, differing widely both from Reptiles and Amphibia as well as from Fish. The skeleton of their four legs, which are transformed into short, broad, paddling fins (like those of fish and whales) furnishes us with a clear proof that the Halisauria branched off from the main-stock of Vertebrata at an earlier period than the Amphibia. For Amphibia, as well as the three higher classes of Vertebrata, are all derived from a common primary form, which possessed only five toes or fingers on each leg. But the Sea-dragons have (either distinctly developed or in a rudimentary condition as parts of the skeleton of the foot) more than five fingers, as have also the Selachians or Primæval fish. On the other hand, they breathed air through lungs, like the Dipneusta, although they always swam about in the sea. They, therefore, perhaps, in conjunction with the Dipneusta, branched off from the Selachii, but did not develop into higher Vertebrata; they form an extinct lateral line of the pedigree, which has died out.
The more accurately known Sea-dragons are classed into three orders, distinct enough one from the other, namely, Primæval Dragons, Fish Dragons, and Serpent Dragons. The Primæval Dragons (Simosauria) are the oldest Sea-dragons, and lived only during the Trias period. The skeletons of many different genera of them are met with in the German limestone known as “Muschel-kalk.” They seem upon the whole to have been very like the Plesiosauria, and are, consequently, sometimes united with them into one order as Sauropterygia. The Serpent Dragons (Plesiosauria) lived in the oolitic and chalk periods together with the Ichthyosauria. They were characterised by an uncommonly long thin neck, which was frequently longer than the whole body, and carried a small head with a short snout. When their arched neck was raised they must have looked very like a swan; but in place of wings and legs they had two pairs of short, flat, oval-paddling fins.
The body of the Fish Dragons (Ichthyosauria) was of an entirely different form; these animals may be opposed to the two preceding orders under the name of Fish-finners (Ichthyopterygia). They possessed a very long extended body, like a fish, and a heavy head with an elongated, flat snout, but a very short neck. Externally, they were probably very like porpoises. Their tail was very long, whereas it was very short in the members of the preceding orders. Also both pairs of paddling fins are broader and show very different structure from that seen in the other two orders. Probably the Fish Dragons and Serpent Dragons developed as two diverging branches out of the Primæval Dragons; but it is also possible that the Plesiosauria alone originated out of the Simosauria, and that the Ichthyosauria were lower off-shoots from the common stock. At all events, they must all be directly, or indirectly derived from the Selachii, or Primæval fish.
The succeeding classes of Vertebrata, the Amphibia and the Amniota (Reptiles, Birds, and Mammals), owing to the characteristic structure which they all exhibit of five toes to each foot, may all be derived from a common primary form, which originated from the Selachii, and which possessed five toes on each of its four limbs. When we find a less number of toes than five, we can show that the missing ones must have been lost in the course of time by adaptation. The oldest known Vertebrata with five toes are the Batrachias (Amphibia). We divide this class into two sub-classes, namely, mailed Batrachians and naked Batrachians, the first of which is distinguished by the body being covered with bony plates or scales.




