Abstract
According to current classification, the living amphibians are distributed among three orders—Caudata (newts and salamanders, or urodeles), Gymnophiona (caecilians), and Anura (frogs and toads)—which often are grouped in a single subclass—Lissamphibia. A current summary of the biology of the Lissamphibia is found in Duellman and Trueb (1994). Among the morphological features common to the three orders of Lissamphibia, but lacking in fish, are four evidently related to acoustic sensing (see Bolt and Lombard 1992; Fritzsch 1992 for recent reviews): (1) a hole (the oval window) in the bony wall of the otic capsule; (2) the insertion of one or two movable skeletal elements, the columella and the operculum, into that hole from its lateral side; (3) a periotic labyrinth, part of which projects into the hole from its medial side; and (4) two extraordinarily thin membranes (contact membranes), comprising locally fused epithelial linings of the periotic and otic labyrinths, each contact membrane forming part of the wall of a separate papillar recess in the otic labyrinth. The two papillae themselves may be homologues of two sensors found in fish—the macula neglecta and the basilar papilla. In amphibians, the putative homologue of the macula neglecta is called the amphibian papilla. Among fish, the basilar papilla has been found only in the coelacanth fish, Latimeria (Fritzsch 1987).
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