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A combination of divergent natural and sexual selection is a powerful cause of speciation. This conjunction of evolutionary forces may often occur when divergence is initiated by ecological differences between populations because local adaptation to new resources can lead to changes in sexual selection. The hypothesis that differences in resource use contribute to the evolution of reproductive isolation by altering the nature of sexual selection predicts that: (1) differences in sexual traits, such as signals and preferences, are an important source of reproductive isolation between species using different resources; (2) there are identifiable sources of selection on sexual traits that differ between species using different resources; and (3) signals vary between populations using different resources to a larger extent than between populations using the same resource at different localities. Testing these predictions requires a group of closely-related species or populations that specialize on different resources and for which the traits involved in mate choice are known. The Enchenopa binotata species complex of treehoppers (Hemiptera: Membracidae) are host plant specialists in which speciation is associated with shifts to novel host plants. Mating in this complex is preceded by an exchange of vibrational signals transmitted through host plant stems, and the signal traits important for mate choice have been identified. In the E. binotata complex, previous work has supported the first two predictions: (1) signal differences between species are important in mate recognition and (2) host shifts can alter both the trait values favoured by sexual selection and the evolutionary response to that selection. In the present study, we tested the last prediction by conducting a large-scale study of mating signal variation within and between the 11 species in the complex. We find that differences in host use are strongly associated with differences in signal traits important for mate recognition. This result supports the hypothesis that hosts shifts have led to speciation in this group in part through their influence on divergence in mate communication systems.

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Male Graminella nigrifrons leafhoppers (Cicadellidae: Homoptera) employ a "call-fly" strategy to find virgin females on oat host plants. Males observed in isolation during daylight hours exhibit a high rate of interplant movement, calling from the lower canopy on each plant visited. Virgin and mated females exhibit little interplant movement. They differ from one another in that virgin females perch on the upper half of plants, whereas mated females perch on the lower half of plants. The positioning of females in the plant canopy is influenced by light. Unlike mated females, virgin females respond to male calls by emitting their own acoustic signals. When virgin females are present on plants visited by males, interplant movement of males ceases, and a localized-upward search of the female bearing plant ensues. Male search is influenced by light. Regardless of whether virgin females were confined to the upper or lower portion of plants, direction of male search was towards a light source used to illuminate above or below the plant canopy. These findings suggest that interplant movement by males and sedentary behavior by females prior to mate recognition and their use of acoustic and phototactic sensory modalities after mate recognition represent previously unrecognized adaptations to problems associated with the use of vibrational signals on plants.

The influences of artificial and natural rearing substrates on mating success were investigated for the parasitoid wasp Cotesia marginiventris (Cresson) (Hymenoptera: Braconidae), a candidate for augmentative biological control of various lepidopteran pests. Five rearing substrates were tested: plastic, glass, chiffon fabric, and leaves of two host plants, bean [ Vigna unguiculata (L.) (Fabaceae)] and maize [ Zea mays L. (Poaceae)]. Mating success was highest on chiffon, lowest on plastic and glass, and intermediate on maize and bean. The transmission characteristics of one component (buzz 1) of the courtship vibrations produced by male wing fanning were investigated using laser vibrometry. The duration of buzz 1 was longer on maize, bean, and chiffon than on plastic and glass. The fundamental frequency of buzz 1 (~300 Hz) was lowest on bean and highest on glass, and intermediate among other substrates. The relative amplitude of buzz 1 was higher on chiffon than on plastic, glass, or bean, and intermediate on maize. The relative importance of airborne sound and substrate vibration as courtship signals was also investigated with experiments that manipulated the production of courtship vibrations and the mating substrates. The amplitude of courtship vibrations on chiffon was significantly higher for winged males than for dealated males. The mating success of males was impacted by both the presence of wings and the mating substrate. These findings suggest that mating success and transmission of courtship vibrations are influenced by the rearing substrate, and that courtship vibrations are critical to mating success in C. marginiventris . Future efforts to mass rear this parasitoid and other insects should consider the potential influences of rearing substrates on mating.