Oviductal retention of developing embryos, with provision for maternal
nutrition after yolk is exhausted (viviparity) and maintenance throug
h metamorphosis, has evolved independently in each of the three living
orders of amphibians, the Anura (frogs and toads), the Urodela (salam
anders and newts), and the Gymnophiona (caecilians). In anurans and ur
odeles obligate viviparity is very rare (less than 1% of species); a f
ew additional species retain the developing young, but nutrition is yo
lk-dependent (ovoviviparity) and, at least in salamanders, the young m
ay be born before metamorphosis is complete. However, in caecilians pr
obably the majority of the approximately 170 species are viviparous, a
nd none are ovoviviparous. All of the amphibians that retain their you
ng oviductally practice internal fertilization; the mechanism is cloac
al apposition in frogs, spermatophore reception in salamanders, and in
tromission in caecilians. Internal fertilization is a necessary but no
t sufficient exaptation (sensu Gould and Vrba: Paleobiology 8:4-15, '8
2) for viviparity. The salamanders and all but one of the frogs that a
re oviductal developers live at high altitudes and are subject to rigo
rous climatic variables; hence, it has been suggested that cold might
be a ''selection pressure'' for the evolution of egg retention. Howeve
r, one frog and all the live-bearing caecilians are tropical low to mi
ddle elevation inhabitants, so factors other than cold are implicated
in the evolution of live-bearing. Viviparity might facilitate life in
a rigorous environment, but likely is not ''caused'' by such an existe
nce. (C) 1993 Wiley-Liss, Inc.