In order to observe amphibian larvae in development, the normal table of development of them is nesessary. Developing larvae can be classified into several stages according to the lenght of body or time after fertilization but these methods seem to get a variety in each stage. Any examination of the gloss external features of body changes is relevant to a classification. In this study, each specimens, Bufo japonicus, were devided into several stages in accordance with the normal table of development of Bufo japonicus by Iwasawa and their ears were observed morphologically under light microscopy.
The development of the inner ear
At the time of hatching (about stage 21), the otic placord has been formed and has led the otic vesicle during stage 22 to 26. At stage 27, the recessus labyrinthi has developed at the dorsomedial side of the otic veside and has become later the ductus and saccus endolymphaticus. At stage 28, the otic veside is devided into two parts by septum, representing respectively utriculus and sacculus. At the same time, the tree semicircular canals have been separeted from the utriculus and have been completed at stage 34. In the sacculus, the maculae lagenae and sacculi and the papillae amphibiorum and basilaris are formed at stage 33 to 34. The inner ear has been almost completed by the initiation of swimming and eating activity (about stage 34).
The development of the middle ear and its surrouding cirgans
At stage 37, the operculum begins to from as a mesenchymal condensation in the posterior portion of the fenestra ovalis. This condensation begins to condrify and becames a cartilaginous flat plate. By stage 41, the operculum has been formed. The completion of the opercular system is consistent with the connection of the opercular muscle between the scapula and the operculum. The formation of the opercular system is coincide with forelimb development. At the timing of the completion of the operculum (stage 41), the columella (stapes) has been formed as a mesenchymal condensation in the anterior edge of the fenestra ovalis, in contact with the membrane of the fenestra ovalis. The mesenchyme has developed a cartilaginous ball and projected anterolaterally, toward the side of the head. This cartilaginous boll is the proximal portion of the columella. The plectrum has been formed as the ventral extension of the distal portion of the columella, passing underneath the skin that will eventurally form the tynpanic membrane. At the time of begining of the terrestrial life (stage 43 to 44c), dynamic changes have occured in the temporal region. The palatoguadrate and Meckel's cartilage have rotated posteriorly. The tympanic annular cartilage is first formed as a posterior outgrowth of the palatoguadrate near the jow joint. The Meckel's contilage has become to the mandibula and the oro-cleft has grown backward. The thymus, situating laterally to the otic capsule, has begun to move backward during metamorphosis. The otosalpinx and the middle ear cavity have seemed to be formed as the invagination of the pharyngeal mucosa as if replacing the space of the thymus. Most of the investigaters think that the orosalpix and the middle ear cavity come from the first branchial pouch. In this observation, such findings have not been confirmed. As mentioned above, the middle earsound conduction system has been almost completed by the 7th day after the first terrous activity.
The normal table of development of Bufo japonicus ear described in this paper is thought to be useful to the further studies.
Stage 21; neural tube formation III. Stage 22; early tail bud. Stage 26; appearance of gill bud II. Stage 27; ramification of gill bud. Stage 28; simple external gill. Stage 33; operculum formation III. Stage 34; completion of operculum. Stage 37; toe differentiation I. Stage 41; completion of hindlimb. Stage 43; emergence of forelimb I. Stage 44c; vestigial tail. Stage 45;. completion of meta morphosis.
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