Plant can alter reproductive strategies for adaptation to different environments. However, alterations in flowering strategies and sexual allocation for the same species growing in different environments still remain unclear. We examined the sexual reproduction parameters of Caragana stenophylla across four climatic zones from semi-arid, arid, very arid, to intensively arid zones in the Inner M...

Sexual dimorphism is typically a result of strong sexual selection on male traits used in male-male competition and subsequent female choice. However, in social species where reproduction is monopolized by one or a few individuals in a group, selection on secondary sexual characteristics may be strong in both sexes. Indeed, sexual dimorphism is reduced in many cooperatively breeding vertebrates...

Many theories have been proposed to explain the evolution of sex, but the question remains unsettled owing to a paucity of compelling empirical tests. The crux of the problem is to understand the prevalence of sexual reproduction in the natural world, despite obvious costs relative to asexual reproduction. Here we perform experiments with digital organisms (evolving computer programs) to test t...

Although numerous hypotheses exist to explain the overwhelming presence of sexual reproduction across the tree of life, we still cannot explain its prevalence when considering all inherent costs involved. The Red Queen hypothesis states that sex is maintained because it can create novel genotypes with a selective advantage. This occurs when the interactions between species induce frequent envir...

Asexual reproduction, including parthenogenesis in which embryos develop within a female without fertilization, is assumed to confer advantages over sexual reproduction, which includes a "cost of males." Sexual reproduction largely predominates in animals, however, indicating that this cost is outweighed by the genetic and/or ecological benefits of sexuality, including the acquisition of advant...

1. The widespread occurrence of sexual reproduction indicates that the benefits of sex can overcome its costs relative to asexual reproduction. Many closely related sexual and asexual taxa have different geographic distributions suggesting that their relative fitness may depend on the environment. However, support for such ecological differentiation is mainly based on correlative evidence, with...

Cyclic parthenogens, such as the cladoceran, Daphnia magna, utilize both asexual (parthenogenetic) and sexual reproduction in order to maximize population fitness in variable environments. Parthenogenetic reproduction is the default strategy among D. magna, while various environmental cues trigger cycles of sexual reproduction. Experiments were conducted with the juvenile hormone analog methopr...

Cyclical parthenogens, which combine asexual and sexual reproduction, are good models for research into the ecological and population processes affecting the evolutionary maintenance of sex. Sex in cyclically parthenogenetic rotifers is necessary for diapausing egg production, which is essential to survive adverse conditions between planktonic growing seasons. However, within a planktonic seaso...

Facultatively sexual organisms often engage in sex more often when in poor condition. We show that such condition-dependent sex carries evolutionary advantages and can explain the evolution of sexual reproduction even when sex entails high costs. Specifically, we show that alleles promoting individuals of low fitness to have sex more often than individuals of high fitness spread through a popul...

Many bacteria are highly sexual, but the reasons for their promiscuity remain obscure. Did bacterial sex evolve to maximize diversity and facilitate adaptation in a changing world, or does it instead help to retain the bacterial functions that work right now? In other words, is bacterial sex innovative or conservative? Our aim in this review is to integrate experimental, bioinformatic and theor...