Sexual Selection History Research Articles

Pesticide exposure triggers sex-specific inter- and transgenerational effects conditioned by past sexual selection.

Environmental variation often induces plastic responses in organisms that can trigger changes in subsequent generations through non-genetic inheritance mechanisms. Such transgenerational plasticity thus consists of environmentally induced non-random phenotypic modifications that are transmitted through generations. Transgenerational effects may vary according to the sex of the organism experiencing the environmental perturbation, the sex of their descendants or both, but whether they are affected by past sexual selection is unknown. Here, we use experimental evolution on an insect model system to conduct a first test of the involvement of sexual selection history in shaping transgenerational plasticity in the face of rapid environmental change (exposure to pesticide). We manipulated evolutionary history in terms of the intensity of sexual selection for over 80 generations before exposing individuals to the toxicant. We found that sexual selection history constrained adaptation under rapid environmental change. We also detected inter- and transgenerational effects of pesticide exposure in the form of increased fitness and longevity. These cross-generational influences of toxicants were sex dependent (they affected only male descendants), and intergenerational, but not transgenerational, plasticity was modulated by sexual selection history. Our results highlight the complexity of intra-, inter- and transgenerational influences of past selection and environmental stress on phenotypic expression.

Finding love: fruit fly males evolving under higher sexual selection are inherently better at finding receptive females

Courtship is an important component of male reproductive behaviour that enables males to learn about the suitability of their mating partners. Experimental evidence suggests that Drosophila melanogaster males can learn to modify their courtship behaviour based on their prior experience with unreceptive females. This courtship learning is expected to provide a fitness advantage to males and could therefore evolve given suitable heritable variation. We investigated the role of sexual selection in the evolution of courtship learning ability of males, using populations of D. melanogaster evolving under high and low levels of sexual selection for over 170 generations. We exposed males from both types of population to unreceptive females and then tested their ability to discriminate between receptive and unreceptive females in a complex mating environment. After being exposed to unreceptive females, males from both types of population (1) courted females less (both receptive and unreceptive), (2) took longer to initiate courtship, but took less time to start mating after initiating courtship and (3) increased the proportion of courtship directed towards receptive females, indicating the ability of both types of males to learn from previous experience. We did not find any difference in the courtship learning ability of males from the two types of populations. However, males from populations with higher levels of sexual selection were better at recognizing and courting receptive females, even when they were not previously exposed to unreceptive females. Taken together, these results show that sexual selection may not result in improved learning abilities but can lead to the evolution of an improved innate ability of males to assess the receptivity of females. • Selectively courting receptive females can greatly affect the fitness of males. • Courtship learning enables males to assess the receptivity of females. • History of sexual selection does not affect the males' courtship learning ability. • Males evolving under higher sexual selection recognize receptive females better. • Courtship learning affected courtship and mating latency and courtship intensity.

An unexpectedly long history of sexual selection in birds-of-paradise

BackgroundThe birds-of-paradise (Paradisaeidae) form one of the most prominent avian examples of sexual selection and show a complex biogeographical distribution. The family has accordingly been used as a case-study in several significant evolutionary and biogeographical syntheses. As a robust phylogeny of the birds-of-paradise has been lacking, these hypotheses have been tentative and difficult to assess. Here we present a well supported species phylogeny with divergence time estimates of the birds-of-paradise. We use this to assess if the rates of the evolution of sexually selected traits and speciation have been excessively high within the birds-of-paradise, as well as to re-interpret biogeographical patterns in the group.ResultsThe phylogenetic results confirm some traditionally recognized relationships but also suggest novel ones. Furthermore, we find that species pairs are geographically more closely linked than previously assumed. The divergence time estimates suggest that speciation within the birds-of-paradise mainly took place during the Miocene and the Pliocene, and that several polygynous and morphologically homogeneous genera are several million years old. Diversification rates further suggest that the speciation rate within birds-of-paradise is comparable to that of the enitre core Corvoidea.ConclusionThe estimated ages of morphologically homogeneous and polygynous genera within the birds-of-paradise suggest that there is no need to postulate a particularly rapid evolution of sexually selected morphological traits. The calculated divergence rates further suggest that the speciation rate in birds-of-paradise has not been excessively high. Thus the idea that sexual selection could generate high speciation rates and rapid changes in sexual ornamentations is not supported by our birds-of-paradise data. Potentially, hybridization and long generation times in polygynous male birds-of-paradise have constrained morphological diversification and speciation, but external ecological factors on New Guinea may also have allowed the birds-of-paradise to develop and maintain magnificent male plumages. We further propose that the restricted but geographically complex distributions of birds-of-paradise species may be a consequence of the promiscuous breeding system.

The secondary copulatory organ in female ground weta (Hemiandrus pallitarsis, Orthoptera: Anostostomatidae): a sexually selected device in females?

Secondary sexual devices in female insects, primarily abdominal modifications, appear to function as a means of thwarting coercive mating attempts by males or are, in rare cases, sexually selected adaptations. Female ground weta, Hemiandrus pallitarsis (Orthoptera: Anostostomatidae), have an elaborate elbowed device on the underside of the mid-abdomen. Experimental removal of this accessory organ shows that it does not increase the probability of mating as predicted by the thwart-copulation hypothesis. Instead, removal prevents copulation, thus demonstrating that it is a secondary copulatory device. The male attaches to the organ both at the beginning of copulation and at the end, when he positions himself to adhere a spermatophylax food gift onto the mid-ventral region of his mate. The female accessory organ does not function to manipulate eggs or larvae (females provide care to their single clutch of offspring) and is unlikely to be a copulatory structure that prevents hybridization. The great extent of the modification of the ventral abdominal segments of H. pallitarsis females compared to other Hemiandrus species is consistent with a history of sexual selection on the accessory organ. Taken together, these results and the finding that the length of the accessory organ of H. pallitarsis correlates with female fecundity, suggest that this structure evolved under sexual selection to acquire nuptial gifts from males.

Variation at the major histocompatibility complex in Savannah sparrows.

The class I and class II genes of the major histocompatibility complex (Mhc) encode dimeric glycoproteins responsible for eliciting the adaptive immune response of vertebrates. Recent work with birds suggests that the number, size, and arrangement of these genes can differ markedly across species, although the extent of this variation, and its causes and consequences, are poorly understood. We have used a 157-base-pair (bp) portion of the second exon of a class II B gene to probe the Mhc in a free-living population of Savannah sparrows (Passerculus sandwichensis). Segregation analysis of Mhc bands suggests that class II B genes can be found in two independently assorting clusters, as previously described for domestic chickens (Gallus gallus) and ring-necked pheasants (Phasianus colchicus) but unlike gene organization in mammals. The Mhc in Savannah sparrows appears large (with many class II B genes) and variable; we found 42 unique genotypes among 48 adults breeding on Kent Island, New Brunswick, Canada in 1995. Savannah sparrows are long-distance migrants, and these results support recent predictions that migratory birds should show higher levels of Mhc polymorphism and/or a greater number of genes than sedentary species. Savannah sparrows are also socially polygynous with high levels of extra-pair paternity, suggesting that a history of sexual selection might also influence the size and/or structure of the avian Mhc.

Facial attractiveness, developmental stability, and fluctuating asymmetry

Despite robust cross-cultural reliability of human facial attractiveness ratings, research on facial attractiveness has only superficially addressed the connection between facial attractiveness and the history of sexual selection in Homo sapiens. There are reasons to believe that developmental stability and phenotypic quality are related. Recent studies of nonhuman animals indicate that developmental stability, measured as fluctuating asymmetry in generally bilateral symmetrical traits, is predictive of performance in sexual selection: Relatively symmetrical males are advantaged under sexual selection. This pattern is suggested by our study of facial attractiveness and fluctuating asymmetry in seven bilateral body traits in a student population. Overall, facial attractiveness negatively correlated with fluctuating asymmetry; the relation for men, but not for women, was statistically reliable. Possible confounding factors were controlled for in the analysis.