The costs of mating and egg production in Callosobruchus seed beetles (original) (raw)
Related papers
2009
Although there is continuing debate about whether sexual selection promotes or impedes adaptation to novel environments, the role of mating behavior in such adaptation remains largely unexplored. We investigated the evolution of mating behavior (latency to mating, mating probability and duration) in replicate populations of seed beetles Callosobruchus maculatus subjected to selection on life-history ("Young" vs. "Old" reproduction) under contrasting regimes of sexual selection ("Monogamy" vs. "Polygamy"). Life-history selection is predicted to favor delayed mating in "Old" females, but sexual conflict under polygamy can potentially retard adaptive life-history evolution. We found that life-history selection yielded the predicted changes in mating behavior, but sexual selection regime had no net effect. In within-line crosses, populations selected for late reproduction showed equally reduced early-life mating probability regardless of mating system. In between-line crosses, however, the effect of lifehistory selection on early-life mating probability was stronger in polygamous lines than in monogamous ones. Thus, although mating system influenced male-female coevolution, removal of sexual selection did not affect the adaptive evolution of mating behavior. Importantly, our study shows that the interaction between sexual selection and life-history selection can result in either increased or decreased reproductive divergence depending on the ecological context.
The effects of age at mating on female life-history traits in a seed beetle
Behavioral Ecology, 2007
Age at first reproduction is an important component of life history across taxa and can ultimately affect fitness. Because genetic interests of males and females over reproductive decisions commonly differ, theory predicts that conflict may arise over the temporal distribution of matings. To determine the potential for such sexual conflict, we studied the direct costs and benefits associated with mating at different times for females, using seed beetles (Acanthoscelides obtectus) as a model system. Virgin females were resistant to male mating attempts at a very early age but subsequently reduced their resistance. Although we found no difference in life span or mortality rates between females mated early in life and those mated later, females that mated early in life suffered a 12% reduction in lifetime fecundity. Thus, there are direct costs associated with mating early in life for females. Yet, males mate even with newly hatched females. We suggest that these data indicate a potential for sexual conflict over the timing of first mating and that female resistance to mating, at least in part, may represent a female strategy aimed at delaying mating to a later time in life.
Does seed size mediate sex-specific reproduction costs in the Callosobruchus maculatus bean beetle?
PLOS ONE
There is a trade-off between reproductive effort and adult longevity, and when resource allocation is taken into account, it is especially pronounced in species that have aphagous adult forms. This trade-off may be further complicated by environmental factors such as nutrient availability during larval development and by the other sex, which influences the costs of reproduction due to the presentation of nuptial gifts. Here, we examined the influence of larval nutrient quantity on the sex-specific longevity costs of reproduction in the gift-giving seed beetle Callosobruchus maculatus. We found no indication that differences in the nutrient quality of larger and smaller host seeds influence survival in virgin and reproducing individuals or nuptial gift size in reproducing individuals. However, in the case of reproducing individuals, the effect of seed size on survival was statistically marginal. Therefore, we advise taking this into account when investigating reproductive efforts in this species. We have also observed interesting interactions between male and female reproductive costs. While females had generally higher mortality than males, nuptial gifts resulted in lowered female mortality and increased male mortality. Additionally, we found a possibly non-linear relationship between nuptial gift size and the offspring production rate of female recipients.
Sexual selection affects lifespan and aging in the seed beetle
Aging Cell, 2007
Sexual selection in general, and sexual conflict in particular, should affect the evolution of lifespan and aging. Using experimental evolution, we tested whether removal of sexual selection leads to the evolution of accelerated or decelerated senescence. We subjected replicated populations of the seed beetle Callosobruchus maculatus to either of two selection regimes for 35 generations. These regimes either allowed (polygamy) or removed the potential (monogamy) for sexual selection to operate. To test for the evolution of intrinsic differences between the two selection regimes, we assayed longevity in replicate cohorts of virgin females and males. Virgin females from populations evolving under sexual selection had reduced lifespan as predicted by the sexual conflict theory of aging. However, this reduction was due to increased baseline mortality rather than an increase in age-specific mortality rates with age. We discuss these findings in light of other data from this model system and suggest that system-specific idiosyncrasies may often modulate the general effects of male-female coevolution on the evolution of aging.
Multivariate intralocus sexual conflict in seed beetles
Evolution, 2014
Intralocus sexual conflict (IaSC) is pervasive because males and females experience differences in selection but share much of the same genome. Traits with integrated genetic architecture should be reservoirs of sexually antagonistic genetic variation for fitness but explorations of multivariate IaSC are scarce. Previously, we showed that upward artificial selection on male lifespan decreased male fitness but increased female fitness compared with downward selection in the seed beetle Callosobruchus maculatus.
Journal of evolutionary biology, 2014
When males provide females with resources at mating, they can become the limiting sex in reproduction, in extreme cases leading to the reversal of typical courtship roles. The evolution of male provisioning is thought to be driven by male reproductive competition and selection for female fecundity enhancement. We used experimental evolution under male- or female-biased sex ratios and limited or unlimited food regimes to investigate the relative roles of these routes to male provisioning in a sex role-reversed beetle, Megabruchidius tonkineus, where males provide females with nutritious ejaculates. Males evolving under male-biased sex ratios transferred larger ejaculates than did males from female-biased populations, demonstrating a sizeable role for reproductive competition in the evolution of male provisioning. Although larger ejaculates elevated female lifetime offspring production, we found little evidence of selection for larger ejaculates via fecundity enhancement: males evolvi...
Although males and females share much of the same genome, selection is often distinct in the two sexes. Sexually antagonistic loci will in theory cause a gender load in populations, because sex-specific selection on a given trait in one sex will compromise the adaptive evolution of the same trait in the other sex. However, it is currently not clear whether such intralocus sexual conflict (ISC) represents a transient evolutionary state, where conflict is rapidly resolved by the evolution of sexual dimorphism (SD), or whether it is a more chronic impediment to adaptation. All else being equal, ISC should manifest itself as correlated evolution between population fitness and SD in traits expressed in both sexes. However, comparative tests of this prediction are problematic and have been unfeasible. Here, we assess the effects of ISC by comparing fitness and SD across distinct laboratory populations of seed beetles that should be well adapted to a shared environment. We show that SD in juvenile development time, a key life-history trait with a history of sexually antagonistic selection in this model system, is positively related to fitness. This effect is due to a correlated evolution between population fitness and development time that is positive in females but negative in males. Loosening the genetic bind between the sexes has evidently allowed the sexes to approach their distinct adaptive peaks.