Genetic polymorphisms are powerful model systems to study the maintenance of diversity in nature. In some systems, polymorphisms are limited to female coloration; these are thought to have arisen as a consequence of reducing male mating harassment, commonly resulting in negative frequency‐dependent selection on female color morphs. One example is the damselfly Ischnura elegans, which shows three female color morphs and strong sexual conflict over mating rates. Here, we present research integrating male tactics, and female evolutionary strategies (female mating behavior and morph‐specific female fecundity) in populations with different morph‐specific mating frequencies, to obtain an understanding of mating rates in nature that goes beyond the mere measure of color frequencies. We found that female morph behavior differed significantly among but not within morphs (i.e., female morph behavior was fixed). In contrast, male tactics were strongly affected by the female morph frequency in the population. Laboratory work comparing morph‐specific female fecundity revealed that androchrome females have lower fecundity than both of the gynochrome female morphs in the short term (3‐days), but over a 10‐day period one of the gynochrome female morphs became more fecund than either of the other morphs. In summary, our study found sex‐specific dynamics in response to different morph frequencies and also highlights the importance of studying morph‐specific fecundities across different time frames to gain a better understanding of the role of alternative reproductive strategies in the maintenance of female‐limited color polymorphism.

ABSTRAGT Spodoptera frugiperda (J.E.Smith) (Lepidoptera: Noctuidae) is a Neotropical moth that has diverged into corn. Zea mays L., and rice, Oryza sativa L., host strains because these plants are their most frequently used hosts. The corn strain also has been found in cotton, Gossypium hirsutum L., and sorghum. Sorghum bicolor (L. ) Moench, and the rice strain in small grasses and pasture grasses. Studies of the reproductive isolation between these two strains have provided ambiguous results from populations in the United States. In Golombia, we tested pre-and postzygotic isolation in these strains. Both strains showed postzygotic isolation for several life-history traits, including nutnber of egg masses, number of larvae, number of females, pupal developmental time, female and male longevity, and female and male pupal weight. We observed a reduction of the number of hybrid females and a reduction in fertility in hybrids in S. frugiperda. These results suggest tbe possibility of Haldane's lnile. Heterosis in the F^jj) and F^^) generations was observed for number of larvae and adult longevity. This line presented a high standard deviation, suggesting instability in this cross. A possible effect of the X chromosome may explain the reduction in viability and sterility in El hybrids of host strains of S. frugiperda. No temporal isolation was observed between the corn and rice strains. Differences in longevity between corn and rice strains might be another form of temporal isolation between these strains, because differences in adulthood time might reduce the encounters between them and thus hybridization.

A major challenge in evolutionary biology consists of understanding how genetic and phenotypic variation is created and maintained. In this study, we investigated the origin(s) and evolutionary patterns of the female-limited colour polymorphism in ischnuran damselflies. These consist of the presence of one to three colour morphs: one androchrome morph with a coloration that is similar to the male and two gynochrome morphs (infuscans and aurantiaca) with female-specific coloration. We (i) documented the colour and mating system of 44 of the 75 taxa within the genus Ischnura, (ii) reconstructed the evolutionary history of colour and mating system to identify the ancestral state, (iii) evaluated the stability of the colour morph status over time and (iv) tested for a correlation between colour and mating system. We found that the ancestral female colour of Ischnura was monomorphic and aurantiaca and that colour morph status changed over time, characterized by many gains and losses across the species tree. Our results further showed that colour polymorphism is significantly more frequent among polyandric species, whereas monandric species tend to be monomorphic. Research on some Ischnura species has shown that colour morphs have evolved to reduce male mating harassment, and our finding that the same phenotypic morphs have evolved multiple times (convergent evolution) suggests that several species in this genus might be experiencing similar selective pressures.

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