Abstract

Sexual selection is a process that operates through intrasexual competition and intersexual choice for reproduction in both sexes. Here, we report our work on a polygamous moth, Ephestia kuehniella Zeller (Lepidoptera: Pyralidae), aiming to infer the form and nature of precopulatory sexual selection in males and females. We show that, although a number of traits measured in each sex are correlated with mating success, the primary selection trait in females appears to be abdominal thickness and that in males is aedeagus length. As the female's abdominal thickness is a reliable signal about the number and developmental stage of eggs, males who select females with thicker abdomens for mating will gain reproductive benefit, i.e., fertilizing more mature eggs. For females, earlier maturation of their eggs makes the females more likely to achieve mating earlier in an uncertain world where there is no guarantee that they will find more males in the future. Sexual selection appears to be the important force behind the evolution of fast egg maturation in females. We show that, under a male-biased sex ratio, more than 20% of mating fails within a few minutes after the aedeagus has penetrated into the female's genitalia, suggesting that females can assess the features of the male aedeagus before allowing insemination to occur. Dissection and examination of both sexes suggest that a longer aedeagus enhances mating and fertilization efficiency in this species, supporting the notion that sexual selection is a primary force in the evolution of genital variance.

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