Search results for "Sexual conflict"
showing 10 items of 44 documents
Energetically costly precopulatory mate guarding in the amphipod Gammarus pulex: causes and consequences
2003
Precopulatory mate guarding (PCMG) is thought to have evolved as a male mating strategy in species in which female receptivity is limited to a short time. It is common among crustaceans, and energetic costs associated with PCMG are thought to promote size-assortative pairing in such species, although direct evidence is lacking. Using both field surveys and laboratory experiments, we assessed the energetic costs of PCMG in Gammarus pulex and investigated their possible causes. Energetic costs were measured as differences in lipid and glycogen reserves. In field-collected samples, size-corrected lipid and glycogen reserves of paired males were both significantly higher than those of unpaired …
Mating strategies and resulting patterns in mate guarding crustaceans : an empirical and theoretical approach
2012
Because of strong costs associated with each mating event, females are usually not as available for reproduction as males at any given time. Males are therefore in competition with each other for access to receptive females, hence leading to strong sexual selection. One textbook case of such a mating system occurs in moulting crustaceans where females can only be fertilized during a short period following their moult. This has favoured the evolution male strategies to monopolize females before their period of receptivity. Such a precopulatory mate guarding is widespread among many taxa and represents one of the most striking example of males’ competitive traits favoured by sexual selection.…
Male reproductive senescence as a potential source of sexual conflict in a beetle
2011
The link between senescence and reproductive success is a contentious yet crucial issue to our understanding of mate choice, sexual conflict, and the evolution of ageing. By imposing direct (i.e., male fertility) or indirect (i.e., zygote viability) reproductive costs to females, male senescence may lead to sexual conflict at different levels. For example, ageing may affect male ability to deliver sperm, thus setting the scene for sexual conflict over mating, and/or may affect the quality of individual sperm cells, generating the potential for sexual conflict over fertilizing strategies. We addressed these issues by studying the mating behavior, reproductive fitness, and fertilization patte…
It takes two to tango
2003
Abstract In most taxa, females are more likely than males to care for offspring. Why? Ever since Trivers' landmark work, the answer has been traced back to sexual differences in pre-mating reproductive investment (unequal gamete size or anisogamy). However, recent work shows that parental investment theory has inadvertently ignored a profoundly simple fact of life: every offspring has a mother and father. Taking this into account completely changes how we should think about sex differences in parental care.
Can evolution of sexual dimorphism be triggered by developmental temperatures?
2012
Genetic prerequisites for the evolution of sexual dimorphism, sex-specific heritabilities and low or negative genetic correlations between homologous traits in males and females are rarely found. However, sexual dimorphism is evolving rapidly following environmental change, suggesting that sexual dimorphism and its genetic background could be environmentally sensitive. Yet few studies have explored the sensitivity of the genetic background of sexual dimorphism on environmental variation. In this study, on Drosophila melanogaster, we used a large nested full-sib–half-sib breeding design where families were split into four different developmental temperatures: two constant temperature treatme…
Sexual Selection Within the Female Genitalia in Lepidoptera
2015
The genitalia of male and female Lepidoptera are complex organs, composed of several structures that exhibit great diversity of shapes, sizes, and positions, suggesting that they have evolved in a relatively rapid and divergent way. In this chapter, we explore the selective pressures responsible for the evolution of genital morphology in the Lepidoptera , emphasizing the possible role of post-copulatory intersexual selection (PCIS) mechanisms (cryptic female choice and sexual conflict). Our exploration is in great extent speculative because knowledge on the functional morphology of genitalia in this group is limited. We start by describing the complexity and diversity of genitalia in Lepido…
Erratum: Transcriptomes of parents identify parenting strategies and sexual conflict in a subsocial beetle
2016
Parenting in the burying beetle Nicrophorus vespilloides is complex and, unusually, the sex and number of parents that can be present is flexible. Such flexibility is expected to involve specialized behaviour by the two sexes under biparental conditions. Here, we show that offspring fare equally well regardless of the sex or number of parents present. Comparing transcriptomes, we find a largely overlapping set of differentially expressed genes in both uniparental and biparental females and in uniparental males including vitellogenin, associated with reproduction, and takeout, influencing sex-specific mating and feeding behaviour. Gene expression in biparental males is similar to that in non…
The ecology of sexual conflict: behaviorally plastic responses to temperature variation in the social environment can drastically modulate male harm …
2018
AbstractSexual conflict is a fundamental driver of male/female adaptations, an engine of biodiversity, and a crucial determinant of population viability. For example, sexual conflict frequently leads to behavioural adaptations that allow males to displace their rivals, but in doing so harm those same females they are competing to access. Sexual conflict via male harm hence not only deviates females from their fitness optimum, but can decrease population viability and facilitate extinction. Despite this prominent role, we are far from understanding what factors modulate the intensity of sexual conflict, and particularly the role of ecology in mediating underlying behavioural adaptations. In …
Body size and mating strategies in the simultaneous hermaphrodite Oxynoe olivacea (Mollusca, Opisthobranchia, Sacoglossa).
2004
Summary 1To better understand the role and importance of body size in hermaphroditic mating system theory, the mating behaviour of the shelled sacoglossan Oxynoe olivacea was studied. This simultaneous hermaphrodite exhibits bilateral and unilateral sperm transfer and thus it is particularly suitable for studies on hermaphrodite sexual conflict. 2In this study three hypotheses on body size were tested: that O. olivacea partner size has an effect on (i) mating mode choice, (ii) duration of mating modes, and (iii) choice of sexual role. Furthermore, we tested Charnov's hypothesis that in O. olivacea, like many simultaneous hermaphrodites, a sexual conflict exists and the male role is preferre…
Inclusive fitness and sexual conflict: How population structure can modulate the battle of the sexes
2014
Competition over reproductive opportunities among members of one sex often harms the opposite sex, creating a conflict of interest between individual males and females. Recently, this battle of the sexes has become a paradigm in the study of intersexual coevolution. Here, we review recent theoretical and empirical advances suggesting that – as in any scenario of intraspecific competition – selfishness (competitiveness) can be influenced by the genetic relatedness of competitors. When competitors are positively related (e.g. siblings), an individual may refrain from harming its competitor(s) and their mate(s) because this can improve the focal individual's inclusive fitness. These findings r…