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BATRACHIA . The arguments adduced by T. H. See also:Huxley, in his See also:article on this subject in the ninth edition of the Ency 1opaedia Britannia', for applying the name See also:Amphibia to those See also:lung-breathing, pentadactyle vertebrates which had been first severed from the Linnaean Amphibia by See also:Alexandre See also:Brongniart, under the name of Batrachia, have not met with universal See also:acceptance. Although much used in See also:text-books and anatomical See also:works in See also:Great See also:Britain and in See also:Germany, the former name has been discarded; in favour of the latter by the See also:principal authors on systematic herpetology, such as W. See also:Peters, A. See also:Gunther and E. D. See also:Cope, and their See also:lead is followed in the See also:present article. Bearing in mind that See also:Linnaeus, in his use of the name Amphibia, was not alluding to the gill-breathing and See also:air-breathing periods through which most frogs and newts pass in the course of their existence, but only wished to convey the fact that many of the constituents of the See also:group resort to both See also:land and See also:water (e.g. crocodiles), it seems hard to admit that the See also:term may be thus diverted from its See also:original signification, especially when such a See also:change results in discarding the name expressly proposed by Brongniart to denote' the association which has ever since been universally adopted either as an See also:order, a sub-class or a class. Many authors who have devoted See also:special See also:attention to questions of nomenclature therefore think Reptilia and Batrachia the correct names of the two great classes into which the Linnaean Amphibia have been divided, and consider that the latter term should be reserved for the use of those who, like that great authority, the See also:late See also:Professor Peters, down to the See also:time of his See also:death in 1883, would persist in regarding See also:reptiles and batrachians as See also:mere sub-classes (1). However extraordinary it may appear, especially to those who bring the living forms only into See also:focus, that opposition should still be made to Huxley's See also:primary See also:division of the vertebrates other than mammals into See also:Sauropsida (birds and reptiles) and Ichthyopsida (batrachians and fishes), it is certain that See also:recent discoveries in palaeontology have reduced the See also:gap between batrachians and reptiles to such a minimum as to cause the greatest embarrassment in the See also:attempt to draw a satisfactory See also:line of separation between the two; on the other See also:hand the See also:hiatus between fishes and batrachians remains as wide as it was at the time Huxley's article Amphibia (See also:Encyclopaedia Britannica, 9th ed.) was written. The See also:chief See also:character which distinguishes the Batrachians from the reptiles, leaving aside the metamorphoses, lies in the arrangement of the bones of the See also:palate, where a large parasphenoid extends forwards as far or nearly as far as the vomers and widely separates the pterygoids. The bones which See also:bear the two occipital condyles have given rise to much discussion, and the See also:definition given by Huxley in the previous edition—" two occipital condyles, the basi-occipital region of the See also:skull either very incompletely or not at all ossified "—requires revision. Some authors have held that the See also:bone on which the occipital condyles have been found most See also:developed in some labyrinthodonts (2) represents a large basi-occipital bearing two knobs for the See also:articulation with the first vertebra, whilst the skull of the batrachians of the present See also:day has lost the basi-occipital, and the condyles are furnished by the exoccipitals. On the other hand, some reptiles have the occipital condyle divided into two and produced either by the basi-occipital or by the ex-occipitals. But the recent find of a well preserved skull of a labyrinthodont (Capitosaurus stantonensis) from the Trias of See also:Staffordshire has enabled A. S. See also:Woodward (3) to show that, in that See also:form at any See also:rate, the condyles are really exoccipital, although they are separated by a narrow basi-occipital. It is therefore very probable that the authors quoted in (2) were mistaken in their See also:identification of the elements at' the See also:base of the foramen magnum. The fact remains, however, that some if not all of the stegocephalous batrachians have an ossified basi-occipital. As a result of his researches on the anomodont reptiles and the Stegocephalia (4), as the See also:extinct order that includes the well known labyrinthodonts is now called, we have had the proposal by H. G. See also:Seeley (5) to See also:place the latter with the reptiles instead of with the batrachians, and H. Gadow, in his most recent See also:classification (6), places some of them among the reptiles, others being See also:left with the batrachians; whilst H. See also:Credner, basing his views on the See also:discovery by him of various annectent forms between the Stegocephalia and the Rhynchocephalian reptiles, has proposed a class, Eotetrapoda, to include these forms, ancestors of the batrachians proper on the one hand, of the reptiles proper on the other. Yet, that the Stegocephalia, notwithstanding their great See also:affinity to the reptiles, ought to be included in the batrachians as commonly understood, seems sufficiently obvious from the mere fact of their passing through a branchiate See also:condition, i.e. undergoing See also:metamorphosis (7). The outcome of our present knowledge points to the Stegocephalia, probably themselves derived from the Crossopterygian fishes (8), having yielded on the one hand the true batrachians (retrogressive See also:series), with which they are to a certain extent connected through the Caudata and the Apoda, on the other hand the reptiles (progressive series), through the Rhynchocephalians and the Anomodonts, the latter being believed, on very suggestive See also:evidence, to lead to the mammals (9). The division of the class Amphibia or Batrachia into four orders, as carried out by Huxley, is maintained, with, however, a change of names: Stegocephalia, for the assemblage of See also:minor See also:groups that cluster See also:round the Labyrinthodonta of R. See also:Owen, which name is restricted to the forms for which it was originally in-tended; Peromela, Urodela, Anura, are changed to A poda, Caudata, Ecaudata, for the See also:reason that (unless obviously misleading, which is not the See also:case in the present instance) the first proposed name should supersede all others for higher groups as well as for genera and See also:species, and the latter set have the benefit of the See also:law of priority. In the first subdivision of the batrachians into two families by C. Dumeril in 1806 (Zool. Anal. pp. 90-94) these are termed " Anoures " and FIo. 1.- Upper view of Archego-" Urodeles in See also:French, saurus Decheni. (Outlines and Caudati in pm, Praema maxill after st, Sup St p ratem-Latin. When Dumeril's n, Nasal. poral. See also:pupil, M. See also:Oppel, in 1811 m, Maxilla. sq, Squamosal. (Ordn. Rept. P. 72), added 1, Lachrymal. pto, Postorbital. the Caecilians, he named pf, Praefrontal. qi, Quadrato- the three A oda j, See also:J1. fupt groups p j, Jugal. uga o, Occipital. Ecaudata and Caudata. The ptf, Postfrontal. pt, See also:Post-See also:tern- Latin form being the only P, Parietal. poral. one entitled to recognition 4. Quadrate. in zoological nomenclature, it follows that the last-mentioned names should be adopted for the three orders into which recent batrachians are divided. 1. STEGOCEPHALIA (1Q).—Tailed, lacertiform or serpentiform batrachians, with the temporal region of the skull roofed over by postorbital, squamosal, and supratemporal plates similar to the same bones in Crossopterygian fishes, and likewise with paired dermal bones (occipitals and post-temporals) behind the parietals and supratemporals. A parietal foramen; scales or bony scutes frequently present, especially on the ventral region, which is further protected by three large bony plates—interclavicle and clavicles. the latter in addition to cleithra. Extinct, ranging from the Upper Devonian to the Trias. Our knowledge of Devonian forms is still extremely meagre, the only certain See also:proof of the existence of pentadactyle vertebrates at that See also:period resting on the footprints discovered in See also:Pennsylvania and described by O. C. See also:Marsh (11) as Tinopus antiquus. Sundry remains from See also:Belgium, as to the identification of which doubts are still entertained, have been regarded by M. Lohest (12) as evidence of these batrachians in the Devonian. Over zoo species are now distinguished, from the Carboniferous of See also:Europe and See also:North See also:America, the See also:Permian of See also:Spitsbergen, Europe, North America and See also:South See also:Africa, and the Trias of Europe, America, South Africa, See also:India and See also:Australia. The forms of batrachians with which we are acquainted show the vertebral See also:column to have been evolved in the course of time from a notochordal condition with segmented centra similar to that of See also:early bony ganoid fishes (e.g. Caturus, Eurycormus), to biconcave contra, and finally to the socket-and-See also: Embolomeri, with the centra and intercentra equally developed disks, of which there are thus two to each neural arch; these disks perforated in the See also:middle for the passage of the notochord. This type may be directly derived from the preceding, with which it appears to be connected by the genus Diplospondylus. Fam.: CRICOTIDAE, Permian. C. Labyrinthodonta, with See also:simple biconcave vertebral disks, very slightly pierced by a remnant of the notochord and supporting the loosely articulated neural arch. .`' This condition is derived from (Outline after Jaekel.) that of the Rhachitomi, as shown by the structure of the vertebral column in See also:young specimens. Mostly large forms from the Trias (a few Permian), with true labyrinthic dentition. Families: LABY RINTHODONTIDAE, ANTHRACOSAURIDAE, DENDRERPETIDAE, NY RANIIDAE. D. Microsauria, nearest the reptiles, with persistent notochord completely surrounded by constricted cylinders on which the neural arch rests. Teeth hollow, with simple or only slightly folded walls. Mostly of small See also:size and abundant in the Carboniferous and See also:Lower Permian. Families: UROCORDYLIDAE, LIMNERPETIDAE, HYLONOMIDAE (fig. 3), MICROBRACHIDAE, DOLICHOSOMATIDAE; the latter serpentiform, apodal. E. Branchiosauria, nearest to the true batrachians; with persistent non-constricted notochord, surrounded by See also:barrel-shaped, bony cylinders formed by the neural arch above and a pair of intercentra below, both these elements taking an equal See also:share in the formation of a transverse See also:process on each side for the support of the See also:rib. This See also:plan of structure, apparently evolved out of the rhachitomous type by suppression of the pleurocentra and the downward See also:extension of the neural arch, leads to that characteristic of frogs in which, as development shows, the vertebra is formed wholly or for the greater See also:part by the neural arch (14). Small forms from the Upper Carboniferous and Permian formations. A single See also:family: BRANCHIOSAURIDAE. II. APODA (15).—No limbs. Tail vestigial or absent. 'Frontal bones distinct from parietals; palatines fused with maxillaries. Male with an intromittent copulatory, See also:organ. Degraded, See also:worm-like batrachians of still obscure See also:affinities, inhabiting tropical Africa, south-eastern See also:Asia and tropical America. See also:Thirty-three species are known. No fossils have yet been discovered. It has been attempted Af late to do away .with this order altogether and to make the Caecilians merely a family of the Urodeles. This view has originatedout of the very remarkable superficial resemblance between the Ichthyophis-larva and the Amphiuma. Cope (16) regarded the Apoda as the extremes of a line of degeneration from the Salamanders, with Amphiuma as one of the annectent forms. In the See also:opinion of P. and F. See also:Sarasin (17), whose great See also:work on the development of Ichthyophis is one of the See also:moat important recent contributions to our knowledge of the batrachians, Amphiuma is a sort of neotenic Caecilian, a larval form become sexually mature while retaining the branchial respiration. If the See also:absence of limbs and the reduction of the tail were the only characteristic of the group, there would be, of course, no objection to unite the Caecilians with the Urodeles; but, to say nothing of the scales, present in many genera of Apodals and absent in all Caudates, which have been shown by H. Credner to be identical in structure with FIG. 3.—A, Dorsal vertebra of Hytonothose of Stegocephalians, the Caecilian skull pre- See also:mus (side view and front view). B, Dorsal Bents features which are vertebra of Branchiosaurus (side view and not shared by any of front view). n, Neural See also:canal; ch, chorda. the tailed batrachians. (After Credner.) G. M. See also:Winslow (18), who has made a study of the chondrocranium of Ichthyophis, concludes that its condition could not have been derived from a Urodele form, but points to some more See also:primitive ancestor. That this ancestor was nearly related to, if not one of, the Stegocephalians, future discovery will in all See also:probability show. A B North America. This order contains about 150 species, referred to five families: HYLAEOBATRACHIDAE, SALAMANDRIDAE, AMPHIUMIDAE, PROTEIDAE, SIRENIDAE. Fossil remains are few in the Upper See also:Eocene and See also:Miocene of Europe and the Upper Cretaceous of North America. The See also:oldest Urodele known is Hylaeobalrachus Dollo (21) from the Lower Wealdenof Belgium. At present this order is confined to the See also:northern hemisphere, with the exception of two Spelerpes from the See also:Andes of See also:Ecuador and See also:Peru, and a Plethodon from See also:Argentina. IV. ECAUDATA (22).—Frogs and toads. Four limbs and no tail. See also:Radius confluent with ulna, and See also:tibia with fibula; See also:tarsus (astragalus and calcaneum) elongate, forming an additional segment in the See also:hind See also:limb. Caudal vertebrae fused into a urostyle or coccyx. Frontal bones confluent with parietals. This order embraces about 1300 species, of which some 40 are fossil, divided into two sub-orders and sixteen families: A. Aglossa,—Eustachian tubes See also:united into a single ostium pharyngeum; no See also:tongue. DACTYLETH RIDAE, PIPIDAE. B. Phaneroglossa,—Eustachian tubes separated; tongue present. DISCOGLOSSIDAE,PELOBATIDAE, HEMIPHRACTIDAE,AMPHIGNATHODONTIDAE, HYLIDAE, BUFONIDAE, DENDROPHRYNISCIDAE, CYSTIGNATHIDAE, DYSCOPHIDAE,GENYOPHRYNIDAE,ENGYSTOMATIDAE, CERATOBATRACHIDAE, RANIDAE, DENDROBATIDAE. The Phaneroglossa are divided into two groups; Arcifera and Firmisternia, representing two stages of evolution. The family characters are mainly derived from the See also:dilatation or non-dilatation of the sacral diapophyses, and the presence of teeth in one or both jaws, or their absence. The Discoglossidae are noteworthy for the presence of See also:short ribs to some of the vertebrae, and in some other points also they approach the tailed batrachians; they may be safely regarded as, on the whole, the most generalized of known Ecaudata. Distinct ribs are present at an early age in the Aglossa, as discovered by W. G. Ridewood (23). The recent addition of a third genus of Aglossa, Hymenochirus (24) from tropical Africa, combining characters of Pipa and Xenopus, has removed every doubt as to the real affinity which connects these genera. Hymenochirus is further remarkable for the presence of only six distinct pieces in the vertebral column, which is thus the most abbreviated among all the See also:vertebrata. Frogs and toads occur wherever See also:insect See also:food is procurable, and their See also:distribution is a See also:world-wide one, with the exception of many islands. Thus New See also:Caledonia, which has a See also:rich and quite special See also:lizard-See also:fauna, has no batrachians of its own, although the Australian Hyla aurea has been introduced with success. New See also:Zealand possesses only one species (Liopelma hochstetteri), which appears to be rare and restricted to the North See also:Island. The See also:forest regions of See also:southern Asia, Africa and South America are particularly rich in species. According, to our present knowledge, the Ecaudata can be traced about as far back in time as the Caudata. An unmistakable batrachian of this order, refe-red by its describer to Palaeobatrachus, a determination which is only provisional, has been discovered in the Kimmeridgian of the Sierra del Montsech, See also:Catalonia (25), in a therefore somewhat older formation than the See also:Wealden Caudata Hylaeobatrachus. Apart from a few unsatisfactory remains from the Eocene of See also:Wyoming, fossil tailless batrachians are otherwise only known from the Oligocene, Miocene and See also:Pliocene of Europe and India. These forms differ very little from those that live at the present day in the same part of the world, and some of the genera (Discoglossus, Bufo, Oxyglossus, Rana) arc even identical. Palaeobatrachus (26), of which a number of species represented by skeletons of the perfect form and of the See also:tadpole have been described from Miocene beds in Germany, Bohemia and See also:France, seems to be referable to the Pelobatidae ; this genus has been considered as possibly one of the Aglossa, but the absence of ribs in the larvae speaks against such an association. Numerous additions have been made to our knowledge of the development and See also:nursing habits, which are extremely varied, some forms dispensing with or hurrying through the metamorphoses and hopping out of the See also:egg in the perfect condition (27). See also:Skeleton.—In the earliest forms of this order, the Stegocephalia, we meet with considerable variety in the constitution of the vertebrae, and these modifications have been used for their classification. All agree, however, in having each vertebra formed of at least two pieces, the suture between which persists throughout See also:life. In this they differ from the three orders which have living representatives. Even the inferior See also:arches or chevrons of the tail of salamanders are continuously ossified with the centra. As a See also:matter of fact, these vertebrae have no centra proper, that part which should correspond with the centrum being formed, as a study of the development has shown (H. Gadow, 14), by the See also:meeting and subsequent See also:complete co-ossification of the two chief dorsal and ventral pairs of elements (tail-vertebrae of Caudata), or entirely by the pair of dorsal elements. In the Ecaudata, the vertebrae of the See also:trunk are formed on two different plans. In some the notochord remains for a See also:long time exposed along the ventral See also:surface, and, owing to the absence of cartilaginous formation around it, disappears without ever becoming invested otherwise than by a thin elastic membrane; it can be easily stripped off below the vertebrae in larval specimens on the point of metamorphosing. This has been termed the epichordal type. In others, which represent the perichordal type, the greater share of the formation of the whole vertebra falls to the (paired) dorsal See also:cartilage, but there is in addition a narrow ventral or hypo-chordal cartilage which fuses with the dorsal or becomes connected with it by calcified See also:tissue; the notochord is thus completely surrounded by a thick sheath in tadpoles with imperfectly developed limbs. This mode of formation of both the arch and the greater part or whole of the so-called centrum from the same cartilage explains why there is never a neuro-central suture in these batrachians. During segmentation of the dorsal cartilages mentioned above, which send out the transverse processes of diapophyses, there appears between each two centra an intervertebral cartilage, out of which the articulating condyle of the centrum is formed, and becomes attached B either to the vertebra anterior (procoelous type) or posterior (opisthocoelous type) to it, if not remaining as an See also:independent, inter-vertebral, ossified See also:sphere, as we sometimes find in specimens of Pelobatidae. In the Caudata and Apoda, cartilage often persists between the vertebrae; this cartilage may become imperfectly separated into a See also:cup-and-See also:ball portion, the cup belonging to the posterior end of the vertebra. In such cases the distinction between amphicoelous and opisthocoelous vertebrae rests merely on a question of ossi- A fication, and has occasionally given rise to misunderstandings in the use of these terms. Amphicoelous (bi-See also:concave) vertebrae are found in the Apoda and in some of the Caudata; opisthocoelous (convexo-concave) vertebrae in the higher Caudata and in the lower Ecaudata; whilst the great See also:majority of the Ecaudata have procoelous (concavo-See also:convex) vertebrae. All living batrachians, and some of the Stegocephalia, have trans-See also:verse processes on the vertebrae that succeed the See also:atlas (fig. 4), some of which, in the Cau- data, are divided into a dorsal and a ventral portion. Ribs are present in the lower Ecaudata (Discoglossidae and larval Aglossa), but they are never connected with a sternum. It is in fact doubtful whether the .so-called sternum of batrachians, in most cases a mere See also:plate of cartilage, has been correctly identified as such. When limbs are present, one vertebra, rarely two (fig. 5) or three, are distinguished as sacral, giving See also:attachment to the ilia. In the Ecaudata, the form of the transverse processes of the sacral vertebra varies very consider-ably, and has afforded important characters to the systematist. In accordance with the saltatorial habits of the members of this order, the vertebrae, which number from 40 to 60 in the Caudata, to up-wards of 200 in the Apoda, have become reduced to to as the ducens nerves leave the skull. normal number, viz., eight praecaudal, one sacral and an elongate coccyx or urostyle, formed by coalescence of at least two vertebrae. In some genera this coccyx is fused with the ninth vertebra, and contributes to the sy.,, II B (best rp, The rhinal process. pnl, The praenasal processes. an, The alinasal processes, shown by the removal of part of the See also:floor of the left nasal chamber. AO., The antorbital process. pd, The pedicle of the suspensorium continued into cv, the ventral erns of the suspensorium. cd, Its dorsal crus. tt, The tegmen tympani. SE, The sphen-ethmoid. EO., The exoccipitals. Qu.J., The quadratojugal. II. V. VI. Foramina by which the optic; trigeminal and portio dura, and ab- sacrum, whilst in a few others the number of segments is still further reduced by the co-ossification of one or two vertebrae preceding that corresponding to the normal sacral and by the See also:fusion of the two first vertebrae; the extreme of reduction being found in pm, z,. rns. se' the genus Hymenochirus, the vertebral column of which is figured here (fig. 6.) As stated above in the definition of the order, the Stegocephalia have retained most of the See also:cranial bones which are to be found in the Crossopterygian fishes, and it is worthy of See also:note that the bones termed post-temporals may give attachment-to a further bone so prolonged backwards as to suggest the probability of the skull being connected with the See also:shoulder-See also:girdle, as in most teleostome fishes. This sup-position is supported by a specimen from the Lower Permian of See also:Autun, determined as Actinodon frossardi, acquired in 1902 by the See also:British Museum, which shows a bone, similar to the so-called "epiotic See also:cornu " of the microsaurians, Ceraterpeton and Scincosaurus, to have the relations of the supra-cleithrum of fishes, thus confirming a See also:suggestion made by C. W. See also:Andrews (28). As in fishes also, the sensory canal See also:system must have been highly developed on the skulls of many labyrmthodonts, and the impressions left by these canals have been utilized by morphologists for homologizing the various elements of the cranial roof with those of Crossopterygians. The pineal foramen, in the parietal bones, is as constantly present as it is absent in the other orders. Although not strictly forming part of the skull, allusion should be made here to the See also:ring of sclerotic plates which has been found in many of the Stegocephalia, and which is only found elsewhere in a few Crossopterygian fishes as well as in many reptiles and birds. In the orders which are still represented at the present day, the bones of the skull are reduced in number and the " primordial skull," er chondrocranium (fig. 7), remains to a greater or less extent unossified, even in the adult. Huxley's figures of the skull of a caecilian (Ichlhyophis glutinosus), fig. 8, of a perennibranchiate urodele (Necturus maculosus = Menobranchus lateralis), fig. 9, and of a See also:frog (Rana esculenta), fig. to, are here given for comparison. The skull, in the Apoda, is remarkably solid and compact, and it possesses a postorbital or postfrontal bone (marked t in the figure) which does not exist in any of the other living batrachians. The squamosal bone is large and either in contact with the frontals and parietals or separated from them by a vacuity; the See also:orbit is some-times roofed over by bone. The presence, in some genera, of a second See also:row of mandibular teeth seems to indicate the former existence of a splenial See also:element, such as exists in See also:Siren among the Caudata and apparently in the labyrinthodonts. In the Caudata, the frontals remain likewise distinct from the parietals, whilst in the Ecaudata the two elements are fused into one, and in a few forms (Aglossa,, some Pelobalidae) the paired condition of these bones has disappeared in the adult. Prefrontal bones are present in the Salamandridae and Amphiumidae, but absent (or fused with the nasals) in the other Caudata and in the Ecaudata. In most of the former the palatines fuse with the vomers, whilst they remain distinct, unless entirely lost, in the latter. The vomer is single, or absent, in the Aglossa. In the lower See also:jaw of most of the Ecaudata the svmphysial cartilages ossify separately from the dentary bones, forming the so-called mento-meckelian bones; but these symphysial bones, so distinct in the frog, are less so in the Hylidae and Bufonidae, almost indistinguishable in the Pelobalidae and Discoglossidae, whilst in the Aglossa they do not exist any more than in the other orders of batrachians. No batrachian is known to possess an ossified azygous supra-occipital. Although there are four branchial arches in all the larval forms of the three orders, and throughout life in the Sirenidae, the perenni- A B. FIG. 9.—Lateral, dorsal and ventral views of the cranium of Necturus maculosus. See also:Ill the dorsal view, the bones are removed from the left See also:half of the skhh11; in the ventral view, the parasphenoid, palato-pterygoid, and vomers are given in outline. The letters have, for the most part, the same signification as before. seventh See also:nerve. suspensorium. V';V2,V3, First, second and third q, Quadrate process. divisions of the trigeminal. o, Otic process. s.s.l, Stapedio-suspensorial liga- Na, 'Posterior See also:hares. ment. Mck, Meckel's cartilage. h.s.l, Hyo-suspensorial See also:ligament. Gl. (fig. to), The position of the m.h.l, Mandibulo.hyoid Ligament. glottis. Bb', Bbl, Basilbranchials. branchiate Proteidae have only three (see fig. Is). In the adult Apoda these arches and the hyoid fuse into three transverse, curved or angular bones (see fig. 13), the two posterior disconnected from the hyoid. In the Ecaudata, as shown by E. Gaupp (29) and by W. G. Ridewood (30), the whole hyobranebialapparatus forms a cartilaginous continuum, and during metamgrphosis the branchialia disappear without a trace. The hyoid of the adult frog (fig. I2) P.S. 'Lh'.. C EO. P.a. so. PS Au consists of a plate of cartilage with two slender cornua, three processes on each side, and two long bony rods behind, termed the thyro-hyals, which embrace the larynx. In the Aglossa, which are remarkable for the large size and complexity of the larynx, the thyro-hyal bones are incorporated into the laryngeal apparatus, whilst the recently discovered Hymenochirus is further remarkable for the large size and ossification of the hyoidean cornua (ceratohyals), a feature which, though not uncommon among the salamanders, is unique among the Ecaudata (31). The See also:pectoral girdle of the Stegocephalia is, of course, only known from the ossified ele- ments, the identifica- tion of which has given rise to some diversity of opinion. But C. See also:Gegenbaur's (32) inter- pretation may be re- garded as final. He as shown that, as in the Crossopterygian and. Chondrostean ganoid fishes, there di are two clavicular elements on each side; the lower corresponds to the clavicle of See also:rep-tiles and higher vertebrates, whilst the up-per corresponds to the clavicle of teleostean fishes, and has been named by him "cleithrum." As stated above, there is strong evidence in favour of the view that some forms at least possessed in addition a "supracleithrum," corresponding to the supra-clavicle. of bony S fishes. The element often termed " cora- Coid " in these fossils ould be the scapula. he clavicles See also:rest on a D large discoidal, rhom- throughout. the interclavicle of Pmx, Premaxilla. Hy, Hyoidean cornu reptiles. Mx, Maxilla. P.S, Parasphenoid. The pectoral girdle Vo, Vomer. An,Angulare. of the living types of Na, Nasal. D, Dentale. batrachians is dis- S.e, Sphen-ethmoid. V, Foramen of exit tinguishable into a Fr, Frontal. of the trige- scapular, a coracoidal, Pa, Parietal. minal. and a' praecoracoidal E.Q Exoccipital. H, Of the optic. region. In most of the Ep, Epiotic process. X, Of the pneumo- Caudata the scapular Pr.O, See also:Pro-otic. gastric and region alone ossifies, t.t, Tegmentympani. glosso-pharyn- but in the Ecaudata Sq, Squamosal. geal nerves. the coracoid is bony QQ J, Quadrato-jugal. Vr. Foramen by and a clavicle is fre- t', Pterygoid, an- which the or- quently developed over terror process. bito-nasal or the praecoracoid See also:car- Pt2, See also:Internal process. first division of tilage. In these ba- Pts, Posterior or exter- the fifth passes trachians the pectoral nal process. to the nasal arch falls into two dis- Ca, See also:Columella auris. cavity. tinet types—the arci- St, Stapes. ferous, in which the precoracoid (+clavicle) and coracoid are widely separated from each other distally and connected by an arched' cartilage (the ern: coracoid). the right usually overlapping the left ; and the firmi- sternal, in which both precoracoid and coracoid nearly abut on the median line, and are only narrowly separated by the more or less fused epicoracoids. The former type is exemplified by the toads and the lower Ecaudata, whilst the latter is characteristic of the true frogs (Ranidae), although when quite young these batrachians present a condition similar to that which persists throughout life in their lower relatives. A cartilage in the median line in front of the precoracokis, sometimes supported by a bony See also:style, is the so-called omosternum; a large one behind the coracoids, also sometimes provided with a bony style, has been called the sternum. But these names will probably have to be changed when the homologies of these parts are better under-stood. The pelvic arch of some of the Stegocephalia contained a well ossified pubic element, whilst in all other batrachians only the ilium, or the ilium and the ischium are ossified. In the Ecaudata the ilium is greatly elongated and the pubis and ischium are flattened, discoidal, and closely applied to their See also:fellows by their inner surfaces; the pelvic girdle looks like a pair of See also:tongs. The long bones of the limbs consist of an See also:axis of cartilage; the extremities of the cartilages frequently undergo calcification and are thus converted into epiphyses. In the Ecaudata the radius and ulna coalesce into one bone. The carpus, which remains cartilaginous in many of the Stegocephalia and Caudata, contains six to eight elements when the manus is fully developed, whilst the number is reduced in those forms which have only two or three digits. Except in some of the Stegocephalia, there are only four functional digits in the manus, but the Ecaudata have a more or less distinct rudiment of pollex; in the Caudata it seems to be the See also:outer See also:digit which has been suppressed, as atavistic reappearance of a fifth digit takes place on the outer side of the Manus, as it does on the pes in those forms in which the toes are reduced to four. The usual number of phalanges is 2, 2, 3, 2 in the Stegocephalia and Caudata, 2, 2, 3, 3 in the Ecaudata. In the See also:foot the digits usually number five, and the phalanges 2, 2, 3, 3, 2 in the Caudata, 2, 2, , 4, 3 in the Stegocephalia and Ecaudata. There are occasionally See also:intercalary ossifications between the two distal phalanges (33). There are usually nine tarsal elements in the Caudata; this number is reduced in the Ecaudata, in which the two bones of the proximal row (sometimes coalesced) are much elongated and form an additional segment to the greatly lengthened hind-limb, a sort of crus secundarium. In the Ecaudata also, the tibia and fibula coalesce into one bone, and two or three small bones on the inner side of the tarsus form what has been regarded as a rudimentary digit or " prehallux." Integument.—In all recent batrachians, the skin is naked, or if small scales are present, as in many of the Apoda, they are concealed in the skin. The extinct Stegocephalia, on the other hand, were mostly protected, on the ventral surface at least, by an See also:armour of overlapping round, See also:oval, or rhomboidal scales, often very similar to those of Crossopterygian or ganoid fishes, and likewise disposed in trans-verse oblique lines converging forwards on the middle line of the belly. Sometimes these scales assumed the importance of scutes and formed a carapace, as in the batrachian armadillo " discovered by E. D. Cope. A few frogs have the skin of the back studded with stellate bony deposits Phyllomedusa, Nototrema), whilst two genera are remarkable for possessing a bony dorsal See also:shield, See also:free from the vertebrae (Ceratorphrys) or ankylosed to 'them (Brachycephalus). None of the Stegocephalia appears to have been provided with claws, but some living batrachians (Onychodactylus, Xenopus, Hymenochirus) have the tips of some or all of the digits protected by a claw-like horny sheath. The integument of tailed and tailless batrachians is remarkable for the great abundance of follicular glands, of which there may be two kinds, each having a special secretion, which is always more or less acrid and irritating, and affords a means of See also:defence against the attacks of many carnivorous animals. A great See also:deal has been A apparatus of Necturus maculosus. Hh, Hypo-hyal. Ep.br,Ep.b?,Ep.b3, Ch, Cerato-hyal. First, second Bb', First basi- and third epi- branchial. branchials. Bbl, Ossified second Gl, Glottis. basibranchial. published on the poisonous secretion of batrachians (34), which is utilized by the See also:Indians of South America for poisoning their arrows. Some of the See also:poison-secreting glands attain a greater complication of structure and are remarkable for their large size, such as the so-called " parotoid " glands on the back of the See also:head in toads and salamanders. In all larval forms, in the Caudata, and in a few of the Ecaudata (-Xenopus, for instance), the epidermis becomes modified in relation with the termination of sensory nerves, and gives rise to See also:organs of the same nature as those of the lateral line of fishes. In addition to diffuse pigment (mostly in the epidermis), the skin contains granular pigment stored up 2r' in cells, the chromatophores, restricted to the cutis, which are highly See also:mobile and send out r= branches which, by contraction and expansion, may rapidly alter the coloration, most batrachians being in this respect quite comparable to the famous chameleons. Besides See also: Teeth are present in the jaws of all known Stegocephalia view of the head and Apoda and of nearly all Caudata, Siren and trunk of Ichthy- alone presenting plates of See also:horn upon the ophis glutinosus. gingival surfaces of the premaxillae and of Mn, Mandible. the dentary elements of the mandible. But Hy, Hyoid. they are nearly always absent in the lower Br', Br2, 13,4, See also:Bran- jaw of the Ecaudata (exceptions in Hemichial arches. phractus, Amphignathodon, Amphodus, Cerato- GI, Glottis. batrachus, the male of Dimes pho nathus), many Tr, Trachea. of which (toads, for instance) are entirely Ivc, Inferior vena edentulous. cava. - There is great variety in the distribution V, Ventricle. of the teeth on the palate. They may occur Au, Auricles. simultaneously on the vomers, the palatines, Rsve, Lsvc, right the pterygoids and • the parasphenoid in and left supe- some of the Stegocephalia (Dawsonia, Seeleya, rior cavae. Acanthostoma), on the vomers, palatines and Ta, Truncus ar- parasphenoid in many salamandrids (Pletho- teriosus. dontinae and Desmognathinae), on the vomers, A o, Left aortic pterygoids and parasphenoid (some .Pelobates), arch. on the vomers and parasphenoid (Triprion, P.A. Right pulmon- Amphodus), whilst in the majority of other ary artery. The batrachians they are confined to the vomers e See also:rice r d i u m and palatines or to the vomers alone (37). pericardium As regards the alimentary organs; it will extends as far suffice to state, in this very brief See also:sketch, that as the bifurca- all batrachians being carnivorous in their tion of the Perfect condition, the See also:intestine is never very synangium. long and its convolutions are few and simple. But the larvae of the Ecaudata are mainly herbivorous and the See also:digestive See also:tract is accordingly extremely elongate and coiled up like the See also:spring of a See also:watch. The gullet is short, except in the Apoda. The tongue is rudimentary in the perennibranchiate Caudata, well developed, and often protrusile, in the Salamandridae and most of the Ecaudata, totally absent in the Aglossa. The organs of circulation cannot be dealt with here; the most important addition made to our knowledge in recent years being found in the contributions of F. See also:Hochstetter (38) and of G. B.. Howes (39), dealing with the azygous (posterior) See also:cardinal See also:veins in salamanders and some of the Ecaudata. The See also:heart is situated. quite forward, in the gular or pectoral region, even in those tailed batrachians which have a serpentiform body, whilst in the Apoda (fig. t3) it is moved back to .a distance which is comparable to that it occupies in most of the See also:snakes. The See also:Respiratory Organs.—The larynx, which is rudimentary in. most of the Caudata and in the Apoda, is highly developed in the Ecaudata, and becomes the See also:instrument of the powerful See also:voice with which many of the frogs and toads are provided. The lungs are long simple tubes in some of the perenribranchiate Caudata they generally shorten or become cellular in the salamandrids, and attain their highest development in the Ecaudata, especially in such forms as the burrowing Pelobates. Although the lungs are present in such forms as preserve. the gills throughout life, it is highly remarkable that quite a number of abranchiate salamanders, belonging mostly to the subfamilies Desmognathinaeand Plethodonlinae, are devoid of lungs and breathe entirely by the skin and by the bucco-pharyngeal mucose membrane (20). Some of the Salamandrinee show the inter-mediate conditions which have led- to the suppression of the trachea and lungs. In the Apoda, as in many serpentiform reptiles, one of the lungs, either the right or the left, is much less developed than the other, often very short. Urine-genital Organs.—The genital glands, ovaries and testes, are attached to the dorsal wall of the body-cavity, in the immediate vicinity of the kidneys, with which the male glands are intimately connected. The oviducts are long, usually more or less convoluted tubes which open posteriorly into the See also:cloaca, while their anterior See also:aperture is situated far forward, sometimes See also:close to the See also:root of the lung; their walls secrete a gelatinous substance which invests the ova as they descend. In most male batrachians the testes are drained by transverse canals which open into a See also:longitudinal duct, which also receives the canals of the kidneys, so that this See also:common duct conveys both sperma and urine. In some of the discogloesid frogs, however, the seminal duct is quite independent of the See also:kidney;. which has its own canal, or true ureter. Many of the Ecaudata have remnants of oviducts, or Mullerian ducts, most developed in Bufo,. which genus is also remarkable as possessing a problematic organ, See also:Bidder's organ, situated between the testis and the adipose or See also:fat-bodies that surmount it. This has been regarded by some anatomists as a rudimentary ovary. See also:Female salamandrids are provided with a receptaculum seminis. Copulatory organs are absent, except in the Apoda, in which a portion of the cloaca can be everted and acts as a penis. The urinary See also:bladder is always large. The spermatozoa have received a great share of attention, on the part not only of anatomists and physiologists, but even of systematic workers (40). This is due to the great amount of difference in structure and size between these elements in the various genera, and also to the fact that otherwise closely allied species may differ very considerably in this respect. The failure to. obtain hybrids between certain species of Rana has been attributed principally to these See also:differences. The spermatozoa of Discoglossus are remarkable for their great size, measuring three millimetres in length. Pairing and Oviposition.—Batrachians may be divided into four categories under this head:— (t) no amplexation; (2) amplexation. without internal fecundation; (3) amplexation with internal fecundation; (4) copulation proper. The first See also:category embraces many aquatic newts, the second nearly all the Ecaudata, the third the rest of the Caudata, and the See also:fourth the Apoda. In the typical newts (Molge) of Europe, the males are adorned during the breeding See also:season with See also:bright colours and crests or other ornamental dermal appendages, and, resorting to the water, they engage in a lengthy courtship accompanied by lively evolutions around the females,. near which they See also:deposit their spermatozoa in bundles on a gelatinous See also:mass, the spermatophore, probably secreted by the cloacal gland. This arrangement facilitates the internal fecundation of the female without copulation, the, female absorbs the spermatozoa by squeezing them out of the spermatophore between the cloacal lips. Other newts, and many salamanders, whether terrestrial or aquatic, pair, the male embracing the female about the fore limbs or in the pelvic region, and the males of such forms are invariably devoid of ornamental secondary sexual characters; but in spite of this amplexation the same mode of fecundation by means of a spermatophore is resorted to although` it may happen that the contents of the spermatophore are absorbed See also:direct from the cloaca of the male. The spermatozoa thus reach the eggs in the oviducts, where they may develop entirely, some of the salamanders being viviparous. In all the tailless batrachians (with the exception of a single known viviparous See also:toad),the male clings to the female round,the See also:breast, at the See also:arm-pits, or round the See also:waist, and awaits, often for See also:hours or days, the deposition of the ova, which are immediately fecundated by several seminal emissions. The fourth category is represented by the Apoda or Caecilians in which, as we have stated above, the male is provided with an intromittent organ. Some of these batrachians are viviparous. In those species in which the embrace is of long duration the limbs 528 of the male, usually the fore limbs (pleurodele See also:newt, Ecaudata), rarely the hind limbs (a few See also:American and See also:European newts), according to the mode of amplexation, acquire a greater development, and are often armed with temporary horny excrescences which drop off after the pairing season. These asperities usually form See also:brush-like patches on the inner side of one or more of the digits, but may extend over, the inner surface of the limbs and on the breast and See also:chin; the use of them on these parts is sufficiently obvious, but they are sometimes also present, without apparent function, on various parts of the foot, as in Discoglossus, Bombina.tor, and Pelodytes. In some species of the South American frogs of the genus Leptodactylus the breast and hands are armed with very large spines, which inflict deep wounds on the feiiiale held in embrace. In most of the Caudata, the eggs are deposited singly in the axils of water See also:plants or on leaves whic : the female folds over the egg with her hind limbs. The eggs are also deposited singly in some of the lower Ecaudata. In many of the Ecaudata, and in a few of the Caudata and Apoda, the eggs are laid in strings or bands which are twined round aquatic plants or carried by the See also:parent; whilst in other Ecaudata they form large masses which either See also:float on the surface of the water or sink to the bottom. A few batrachians retain the ova within the oviducts until the young have undergone part or the whole of the See also:meta. morphosis. Viviparous parturition is known among the Caudata (Salamandra, Spelerpes fuscus), and the Apoda (Dermophis thomensis, Typhlonectes compressicauda); also in a little toad (Pseudophryne vivipara) recently discovered in See also:German See also:East Africa (41). Development and Metamorphosis.—In a great number of batrachians, including most of the European species, the egg is small and the food-yolk is in insufficient quantity to form an See also:external appendage of the embryo. But in a few European and North American species, and in a great many inhabitants of the tropics, the egg is large and a considerable portion of it persists for a long time as a yolk-See also:sac. Although the segmentation is always complete, it is very irregular in these types, some of which make a distinct approach to the meroblastic egg. With the exception of a number of forms in which the whole development takes place within the egg or in the body of the See also:mother, batrachians undergo metamorphoses, the young passing through a free-See also:swimming, gill-breathing period of considerable duration, during which their See also:appearance, structure, and often their regime, are essentially different from those of the mature form. Even the ' fossil Stegocephalia underwent metamorphosis, as we know from various larval remains first described as Branchiosaurus. They are less marked. or more See also:gradual in the Apoda and Caudata than in Ecaudata, in which the See also:stage known as tadpole is very unlike the frog or toad into which it rather suddenly passes (see TADPOLE). In the Caudata, external gills (three on each side) persist until the close of the metamorphosis, whilst in the Apoda and Ecaudata they exist only during the earlier periods, being afterwards replaced by internal gills. Many cases are known in which the young batrachian enters the world in tht perfect condition, as in the black salamander of the See also:Alps (Salamandra atra), the See also:cave salamander (Spelerpes fuscus), the caeci„an Typhlonectes, and a number of frogs, such as Pipa, Rhino-See also:derma, Hylodes, some Nototrema, Rana opisthodon, &c. A fairly complete See also:bibliographical See also:index to these cases and the most remark-able instances of parental care in tailless batrachians will be found in the interesting articles by Lilian V. See also:Sampson (42), and by G. See also:Brandes and W. Schoenichen (43). It will suffice to indicate here in a synoptic form, as was done by the present writer many See also:year ago, when our knowledge of these wonders of batrachian life was far less advanced than it is now, the principal modes of See also:protection which are resorted to: Protection by means of nests or nurseries. A. In enclosures in the water.—Hylafaber. B. In nests in holes near the water.--Rhacophorus, Lepto(c) On the belly. (1) Exposed, by the female.—Rhacophorus rebiculatus. (2) In a pouch (the produced vocal sac), by the male.—Rhinoderma. (d) In the mouth, by the female.--Hylambates brevirostris. See also:Geographical Distribution.—If a division of the world according to its batrachian faunae were to be attempted, it would differ very considerably from that which would See also:answer for the principal groups of reptiles, the lizards especially. We should have four great realms: (1) Europe and Northern and . Temperate Asia, Africa north of the See also:Sahara (palaearctic region) and North and Central America (nearctic region); (2) Africa and South-Eastern Asia (Ethiopian and See also:Indian region); (3) South America (neotropical region) ; and (4) Australia (Australian region): The first would be characterized by the Caudata, which are almost confined to it (although a few species penetrate into the Indian and neotropical regions), the Discoglossidae, mostly Europaeo-See also:Asiatic, but one genus in See also:California, and the numerous Pelobatidae; the second by the presence of Apoda, the prevalence of firmisternal Ecaudata and the absence of Hylidae ; the third by the presence of Apoda, the pre-See also:valence of arciferous Ecaudata and the scarcity of Ranidae, the fourth by the prevalence of arciferous Ecaudata and the absence of Ranidae, as well as by the absence of either Caudata or Apoda. See also:Madagascar might almost stand as a fifth division of the world, characterized by the See also:total absence of Caudata, Apoda, and arciferous Ecaudata. But the close relation of its very rich frog-fauna to that of the Ethiopian and Indian regions speaks against attaching too great importance to these negative features. It may be noted here that no two parts of the world differ so considerably in their Ecaudata as do Madagascar and Australia, the former having only Firmisternia, the latter only Arcifera. Although there is much similarity between the Apoda of Africa and of South America, one genus being even common to both parts of the world, the frogs are extremely different, apart from the numerous representatives of the widely distributed genus Bssfo. It may be said that, on the whole, the distribution of the batrachians agrees to some extent with that of fresh-water fishes, except for the much less marked affinity between South America and Africa, although even among the former we have the striking example of the distribution of the very natural group of the aglossal batrachians, represented by Pipa in South America and by Xenopus and Hymenochirus in Africa. Synopsis of the Extinct Batrachia of North America," Proc. Ac. Philad., 1868, p. 208. (5) " Researches on the Structure, Organization and Classification of the Fossil Reptilia, vii " Phil. Trans. clxxxiii. (B), 1892, p. 311. (6) See also:Cambridge Natural See also:History, viii. (1901). (7) " See also:Die Urvierfussler (Eotetrapoda) See also:des sachsischen Rotliegenden," Allgem. verstdndl. naturh. Abh., See also:Berlin, 1891, No. 15; " Die Entwicklungsgeschichte von Branchiosaurus amblystomus, Zeitschr.See also:deutsch. geol. Ges., 1886, p. 576. (8) C. See also:Emery, " Ober die Beziehungen des Chiropterygium zum Ichthyopterygium," Zool. Anz. x., 1887, p.. 185; E. D.' Cope, " On the Phylogeny of the Vertebrata," Proc. Amer. Philos. See also:Soc. See also:xxx., 1892, p. 280; H. B. See also:Pollard, " On the See also:Anatomy and Phylogenetic Position of Polypterus," Zool. Jahrb. Anat. v., 1892, p. 414; G. See also:Baur, " The Stegocephali: a Phylogenetic Study," Anat. Anz. xi., 1896, p. 657 ; L. Dollo, " Sur le phylogenie des dipneustes," Mem_ soc. beige geol. ix., 1895, p. 79; T. Gill, " On the Derivation of the Pectoral Member in Terrestrial Vertebrates," Rep. Brit. See also:Ass., 1897, p. 697. (9) E. D. Cope, " The Origin of the See also:Mammalia," Proc. Amer. Philos. Soc. xxu., 1884, p. 43; cf. Discussion on Origin of Mammals, Proc. Intern. Congr. Zool., Cambridge, 1898; also H. Gadow, " The Origin of the Mammalia," Z. f. Morphol. iv., 1902, p. 345; and R. See also:Broom, Rep. Brit. Ass., 1905, p. 437. (10) A. Fritsch, Fauna der Gaskohle and der Kalksteine der Permformation Bohmens, vols. i. and ii (See also:Prague, 1879-1885, 4to) ; H. Credner, " Die Stegocephalen aus dem Rotliegenden des Plauenschen Grundes bei See also:Dresden," Zeitschr. deutsch. geol. Ges., 1881–1894; J. W. See also:Dawson, "On the Results of Recent Explcrations of Erect "Trees containing See also:Animal Remains in the See also:Coal Formation of Nova See also:Scotia," Phil. Trans. clxxiii., 1882, p. 621; H. B. See also:Geinitz and J. V. Deichmuller, " Die Saurier der unteren Dyas von Sachsen," Palaeontegr. See also:xxix., 1882, p.'1; A. See also:Gaudry, See also:Les Enchafnements du monde animal clans let temps geologiques, fossiles primaires (See also:Paris, 1883, 8vo), p. 251; E. D. Cope, " The Batrachia of the Permian Period of North America," Amer. Nat. xviii., 1884, p. 26; E. See also:Fraas, " Die Labyrinthodonten der schwabischen Trias," Palaeontogr. See also:xxxvi., 1889, p. i; L. v. See also:Ammon, Die permischen Amphibien der Rheinpfalz (See also:Munich, 1889-1891, 4to); R. Lydelker,, See also:Catalogue of the Fossil Reptilia and Amphibia in the British Museum, part iv. (See also:London, 189o, 8vo) ; E. Fraas, Die schwabischen Trias-Saurier nach dem Material der k. Naturalien-Sammlung in See also:Stuttgart zusammengestellt (Stuttgart,1896, 4to) ; O. Jaekel, " Die Organization dactylus. C. In nests overhanging the water.—Rhacophorus, Chiromantis, Phyllomedusa. D. On trees or in See also:moss away from the water.—Rana opisthodon, Hylodes, Hylella platycephala. E. In a gelatinous bag in the water.—Phrynixalus, Salamandrella. 2 Direct nursing by the parents. A Tadpoles transported from one place to another.—Dendrebates, Phyllobates, Sooglossus. B. Eggs protected by the parents who coil themselves round or " sit " on them.—Mantophryne, Desmognathus, Autodax, Plethodon, See also:Cryptobranchus, Amphiuma, Ichtkyophis, Hypogeophis, Siphonops. C. Eggs carried by the parents. (a) Round the legs, by the male.—Alytes. (b) On the back, by the female. (1) Exposed.—Hyla goeldii, H. evansii, Ceratohyla (2) In See also:cell-like pouches.—Pipa. (3) In a common pouch.—Nototrema, Amphignathodon. von Archegosaurus," Zeitschr. deutsch. geol. Ges. xlviii., 1896, p. 505; F. Broili, "Ein Beitrag zur Kenntnis von Eryops megacephalus," Palaeontogr. xlvi., 1899, p. 61. (11) " Amphibian Foot-prints from the Devonian," Amer. Journ. Sci. ii., 1896, p. 374. (12) " Decouverte du plus ancien amphibien connu . dans le famennien superieur de Modave," See also:Bull. soc. beige geol. xv., 1888, p. cxx, (13) " A Batrachian Armadillo," Amer. See also:Hat. xxix., 1895, p. 998. (14) C. Gegenbaur, Untersuchungen zur vergleichenden Anatomie der Wirbelsaule bei Amphibian and Replilien (See also:Leipzig, 1862, 4to); H. Gadow, " On the Evolution of the Vertebral Column of Amphibia and Amniota," Phil. Trans. clxxxvii. (B), 1896, p. f. (15) R. Wiedersheim, See also:Pie Anatomic der Gymnophionen (See also:Jena; 1879, 4to); W. Peters, Ober die Einteilung der Caecilien," Mon. Berl. Ac , 1879, p. 924; G. A. Boulenger, Catalogue of Batrachia Gradientia s. Caudata and Batrachia Apoda in the Collection of the British Museum (London, 1882, 8vo), and "A Synopsis cif the Genera and Species of Apodal Batrachians," P.Z.S., 1895, p. 401. (16) " On the Structure and Affinities of the Amphiumidae," Proc. Amer. Philos. Soc. See also:xxiii., 1886, p. 442. (17) Ergebnisse- neturwissenschaftlicher Forschungen auf See also:Ceylon, ii. (See also:Wiesbaden, 1887-189o, 4to). (18) " The Chondrocraniuin of the Ichthyopsida," See also:Stud. Biol. Lab. Tufts See also:Coll. No. 5, 1898, p. 147. (19) G. A. Boulenger, Catalogue, &c., 1882. (20) H. H. Wilder, "Lungenlose Salamandriden," Anat. An.z. ix., 1894, p. 216; L. Camerano, " Ricerche anatomofisiologiche intorno ai Salamandridi normalmente apneumoni," Atti See also:Ace. Torin. ?ocix., 1894, p. 705, and xxxi., 1896, p. 512; H. H. Wilder, " Lung-less Salamanders," Anat. Anz. xii., 1896, p. 182; E. Loennberg, " Notes on Tailed Batrachians without Lungs," Zool. Anz. xix., 1896, p. 33. (21) " Note sur le batracien de Bernissart," Bull. mus. belg. iii., 1884, p. 85. 22) G. A. Boulenger, Catalogue of Batrachia Salientias. Ecaudeta 'in the Collection of the British Museum (London, 1882, 8vo). (23) " On the Development of the Vertebral Column in See also:Pipe and Xenopus," Anat. Anz. xiii., 1898, p. 359. (24) G. A. Boulenger, " On Hymenochirus, a New Type of Aglossal Batrachians," See also:Ann. and Mag. N.H. (7), iv., 1899, p. 122. (25) L. M. Vidal, Mem. Ac. See also:Barcelona (3), iv., 1902, No. 18, pl. iv. (26) W. Wolterstorff, "'Ober fossile Frosche, insbesondere Palacobatrachus," Jahresb. Nat. Ver. Magdeb., 1885 and 1886. (27) W. Peters, "Utter die Entwickelung eincs Batrachiers. Hylodes martinicens'is, ohne Metamornhose," Mon. Berl. Ac., 1876, p. 709; A. 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