The advantage of sex has been among the most debated issues in biology. Surprisingly, the question of why sexual reproduction generally requires the combination of distinct gamete classes, such as small and large gametes, or gametes with different mating types, has been much less investigated. Why do systems with alternative gamete classes (i.e. systems with either anisogamy or mating types or ...

Analyzing regions of the Drosophila genome that have low levels of genetic recombination helps us understand the prevalence of sexual reproduction. Here, we show that genetic variability in these regions can be explained by interference among strongly deleterious mutations and that selection becomes progressively less effective in influencing the behaviour of neighbouring sites as the number of...

If sex is naturally selected as a way to combat parasites, then sexual selection for disease resistance might increase the overall strength of selection for outcrossing. In the present study, we compared how two forms of mate choice affect the evolutionary stability of outcrossing in simultaneous hermaphrodites. In the first form, individuals preferred to mate with uninfected individuals (condi...

François Jacob once facetiously lamented the arrangement in the human body whereby reproduction is the only function for which an individual is equipped with only one-half of the necessary organs, thus entailing the expenditure of a substantial amount of time and energy into finding the other half (10). The spatial separation of the sexual partners (or organs) is indeed an obligatory feature of...

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Although fundamental to the study of invasion mechanisms, the relationship between mode of reproduction and plant invasion is not well understood. Fallopia japonica (Japanese knotweed), a highly aggressive invasive plant in both Europe and North America, serves as a model species for examining this relationship. In Britain, F. japonica var. japonica is a single female clone reproducing solely t...

In sexually dimorphic plants, resource allocation to reproduction often differs between sex morphs. In gynodioecious species, i.e. coexisting hermaphrodite and female plants within a population, females often produce more fruits than hermaphrodites. Since fruit production is costlier than flower production, hermaphrodites and females may regulate flower and fruit production differently in respo...

The evolutionary constraints that lead to the evolution of sexual reproduction are framed by the better repair mechanisms that repair fatal mutations, as well as the need for variable immune systems imposed on large organisms by parasites, such as viruses and bacteria. Besides the evolution of sexual reproduction, these factors also affect mate choice, especially as regards the gene complex tha...

Parthenogenesis has evolved independently in more than 10 Drosophila species. Most cases are tychoparthenogenesis, which is occasional or accidental parthenogenesis in normally bisexual species with a low hatching rate of eggs produced by virgin females; this form is presumed to be an early stage of parthenogenesis. To address how parthenogenesis and sexual reproduction coexist in Drosophila po...

Sexual reproduction in fungi is controlled by genes present at the mating type (MAT) locus, which typically harbors transcription factors that influence the expression of many sex-related genes. The MAT locus exists as two alternative idiomorphs in ascomycetous fungi and sexual reproduction is initiated when genes from both idiomorphs are expressed. Thus, the gene content of this locus determin...