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Ethological reproductive isolation and genetic divergence across 26 protein loci were measured among populations of the salamander Desmognathus ochrophaeus in the southern Appalachian Mountains. Levels of ethological isolation varied from none to complete and were statistically significant for all but two pairings between populations inhabiting different mountain ranges. When geographic and genetic distances were treated as independent variables in multiple correlation analyses, they accounted for about halfthe variance in levels of ethological isolation. When genetic distance is held constant, the remaining relationship between ethological isolation and geographic distance is still statistically significant. When geographic distance is held constant, the remaining relationship between genetic distance and levels of ethological isolation is nonsignificant, as is the relationship between geographic distance and genetic distance when ethological isolation is held constant. Ethological isolation and genetic divergence evidently both reflect the gradual divergence of allopatric populations, but genetic distance is a poor predictor of ethological isolation in these salamanders.

We constructed a model for the evolution of sexual isolation by extending Lande's (1981) model of sexual selection. The model predicts that asymmetric sexual isolation is a transient phenomenon, characteristic of intermediate stages of divergence in sexually selected traits. Unlike the Kaneshiro (1976, 1980) proposal, our model does not depend upon drift and the loss of courtship elements to produce asymmetries in sexual isolation. According to our model, the direction of evolution cannot be predicted from asymmetry in sexual isolation. We tested some features of the model using data from an experimental study of sexual isolation in the salamander Desmognathus ochrophaeus. We tested for sexual isolation between 12 allopatric populations and found significant asymmetry in sexual isolation in about a quarter of the test cases. The highest degrees of asymmetry were associated with intermediate levels of divergence. A curvilinear relationship between isolation asymmetry and divergence was predicted by our model and was supported by statistical analysis of the salamander data.

We constructed a model for the evolution of sexual isolation by extending Lande's (1981) model of sexual selection. The model predicts that asymmetric sexual isolation is a transient phenomenon, characteristic of intermediate stages of divergence in sexually selected traits. Unlike the Kaneshiro (1976, 1980) proposal, our model does not depend upon drift and the loss of courtship elements to produce asymmetries in sexual isolation. According to our model, the direction of evolution cannot be predicted from asymmetry in sexual isolation. We tested some features of the model using data from an experimental study of sexual isolation in the salamander Desmognathus ochrophaeus. We tested for sexual isolation between 12 allopatric populations and found significant asymmetry in sexual isolation in about a quarter of the test cases. The highest degrees of asymmetry were associated with intermediate levels of divergence. A curvilinear relationship between isolation asymmetry and divergence was predicted by our model and was supported by statistical analysis of the salamander data.

With 1 plate and 12 figures in the text) Newts were collected throughout the year from both breeding ponds and terrestrial sites and were weighed, measured and dissected; in males, the testes were examined histologically. Smooth newts show post-nuptial gametogenesis such that, during late summer and autumn they are producing mature gametes for the following year's breeding season. In males, the testes are at their smallest size during the spring, when they consist mostly of immature sperm cysts and evacuated tissue, mature sperm having been evacuated into the vasa deferentia during the newts' migration to water. Evacuated testicular tissue is glandular in function and there is evidence that secretions from this tissue control the development of secondary sexual characters: the dorsal crest, fringes of skin on the toes and the dorsal cloaca1 gland. In both sexes, fat body and liver weights are lowest in the spring and increase in the autumn. In females, oocytes vary in size, depending on the amount of yolk they contain. Only the larger oocytes are laid in a current breeding season, the smaller ones being retained and yolked in late summer and autumn. In both sexes, measures of fecundity (testis size in males, oocyte number in females) are strongly correlated with body size. The finding that male newts have a finite supply of sperm during the breeding season leads to an interpretation of various aspects of male courtship behaviour. These are adaptations for conserving sperm and allocating it to courtship encounters in a way likely to promote male reproductive success.

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