Abstract

The present study investigates the coevolution of a particular male genital process and the female spermathecal ducts in a clade of stalk-eyed flies (Diptera, Diopsidae) and debates the underlying evolutionary mechanisms. The fine morphology and interaction of the male and female genitalic structures are reconstructed from serial sections of mating pairs in one of the species. It is found that the male genital process traverses the common spermathecal duct to enter the base of one of the separate spermathecal ducts during the mating. Spermatozoa and accessory secretions are not transferred through the male genital process but can be discharged only from the male gonopore near its base. A detailed morphometric study reveals low intraspecific variation and hypoallometry of the male genital process. Across 17 species studied comparatively, the lengths of the male genital process and the female common and separate spermathecal ducts are highly variable. The length of the male genital process is correlated significantly with that of the female common spermathecal duct, but not with that of the separate spermathecal ducts. Based on the combined evidence it is concluded that the male genital process and the female common spermathecal duct have coevolved, and that sexual selection by cryptic female choice constitutes a possible and parsimonious explanation for their coevolution. Alternative or additional explanations in terms of sexually antagonistic coevolution cannot be ruled out conclusively, but are not supported by the available evidence.

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