The figure (see [fig. 6]) is a composite picture of the lateral-line system of the higher or truly stegocephalous Amphibia. The outline of the skull is based on that of Eryops. All of the canals do not exist on any one skull or in any one order, but all are found somewhere in the group.
Fig. 11.
A. Skull of Eoserpeton tenuicorne Cope, showing arrangement of cranial elements. × 2. fr, frontal; j, jugal; mx, maxilla; n, nasal; or, orbit; par, parietal; pof, postfrontal; pmx, premaxilla; po, postorbital; pp, postparietal; qj, quadratojugal; sq, squamosal; spt, supratemporal; tab, tabulare.
B. Outline of skull of Ceraterpeton galvani Huxley from the Carboniferous of England. Heavy broken lines show the distribution of lateral-line canals. × 1. (After Andrews.) fr, frontal; par, parietal; or, orbit; po, postorbital; pp, postparietal; spt, supratemporal; tab, tabulare.
The canals have been described in all known orders of fossil Amphibia and the system is found likewise in all the living orders, including the Gymnophiona, which have "a strong line of lateral sense-organs" (Gadow). In the Branchiosauria, the earliest of the true Amphibia (Euamphibia) and ancestral to the modern Caudata, the lateral-line system is known on the tails of two genera ([462], [478]) from the Mazon Creek, Illinois, shales—Micrerpeton and Eumicrerpeton. The system as there defined has been fully discussed in the description of the anatomical details of the species, to which reference may be made for further data ([pp. 52-60]). Suffice it to say here that the system of sense-organs there preserved is identical with that of the larval Necturus; the lines arising as a median from the tip of the tail and a dorsal springing from the median at a distance of a few millimeters from the tip of the tail. The lines are more evident on account of the fact that the lateral-line sense-organs were located under specialized pigmented scales. The significance of the close similarity between the arrangement of the lateral-line systems on the tail of Necturus, Micrerpeton, and Eumicrerpeton is doubtless of genetic ([459]) importance, indicating the origin of the caudate Amphibia from the Branchiosauria by a degenerative or recessive evolution in other structural characters. This system of sense-organs has been described in no other branchiosaurian.
The Microsauria ([458]) are exceedingly interesting in possessing a very peculiar type of lateral-line system. It is known in a few forms and in one specimen especially well (Erpetosaurus tabulatus) ([fig. 22, G]). In this species, which is represented by a single imperfect skull, there are evidences of a nearly complete lateral-line system of canals and pits. The occipital cross-commissure is represented on the posterior border of the skull by a row of elongate pits such as Andrews described for Ceraterpeton ([8]). I fail to find in American species the pores described by Andrews. The temporal canal forms with the jugal canal a complete ring, much as it is in Trematosaurus, only in Erpetosaurus tabulatus the temporal canal does not touch the tabulare. I think there are indications of a connection of the temporal canal with the supraorbital. The temporal canal cuts the supratemporal, the squamosal, and jugal. The jugal canal lies for the most part on the supratemporal and quadratojugal, and joins the infraorbital on the jugal. A portion only of the infraorbital canal is preserved. There is also a portion of the supraorbital canal. It seems not to be connected with the temporal canal, although there is a possible indication of this connection. The supraorbital crosses the frontal, prefrontal, and a part of the nasal. The squamosal element is peculiar in Erpetosaurus tabulatus in that it is excluded from the parietal by the extension of the tabulare and postorbital. This condition is found in several other species of the Microsauria. It will be noticed that with the changed condition of the squamosal the temporal canal has changed also, and this is further proof of the close connection between the cranial elements and the lateral-line canals, as Allis has maintained for Amia. (See in this connection C. J. Herrick, Journ. Comp. Neurol., vol. II, p. 224, 1901.)
The Diplocaulia, an amphibian order allied to the Branchiosauria ([477]) and through them to the Caudata, have the lateral-line system apparently well-developed. The skulls are always crushed flat, so that the canals are nearly obliterated. On the mandible, however, the canals are clearly distinct and apparently run the entire course around the mandibular rami. On a well-preserved skull of Diplocaulus magnicornis Cope there are indications of three lateral-line canals ([477, pl. 1]). The infraorbital is clearly marked as a well-defined groove just below the orbit. The supraorbital is indicated only for a short distance, and there are indications of the temporal canal. The operculo-mandibular canal has its course, for the most part, near the middle of the rami, but as it approaches the posterior angle of the mandible it suddenly changes its course and drops down to the lower edge, only to rise again and to come out strongly marked near the median plane on the posterior angle of the mandible.
The Temnospondylia, as represented by Eryops, Cricotus, and Archegosaurus, possess well-developed lateral-line canals ([458]). H. von Meyer ([428]) many years ago made out the course of the canals in Archegosaurus. The greater part of the following description is based on Eryops megacephalus Cope from the Texas Permian. The entire surface of the cranial elements in Eryops, as in other of the Stegocephala ([458]), is covered with coarse pits. The fossæ are present even in the bottoms of the grooves which represent the lateral-line system, and are more marked in the members of the Temnospondylia than in the Stereospondylia.