124 research outputs found

    Life-history traits as causes or consequences of social behaviour: why do cooperative breeders lay small clutches?

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    Cooperatively breeding birds tend to exhibit high adult survival and relatively small clutch sizes. According to the life-history hypothesis for cooperative breeding, high survival creates conditions for philopatry based on difficulties that dispersers face when competing for territories in a landscape with slow territory turnover. However, this hypothesis evokes a puzzle because high fecundity should also lead to problems in territory acquisition because of the large number of competitors for each vacancy. We suggest two reasons for the observed association between small clutch size, high survival rate and cooperative breeding in birds. The first reason is that when survival rate is a better predictor of cooperative breeding than fecundity, a general life-history trade-off between clutch size and survival rate will create the observed association between cooperative breeding and the two life-history characters. Theoretically, a high survival rate is expected to predict cooperative breeding better than fecundity, because a high survival rate increases both habitat saturation and the direct benefits of staying at home. The second reason is that the reproductive value of the first offspring each year is higher than that of subsequent offspring for cooperative breeders (the offspring depreciation hypothesis). This is because these offspring will be able to delay dispersal and gain indirect benefits by helping at home. We show that this. under very general conditions, decreases the optimum clutch size of cooperative breeders below that of non-cooperative breeders

    Male mating constraints affect mutual mate choice: Prudent male courting and sperm limited females

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    Costs of sperm production may lead to prudence in male spermallocation and also to male mate choice. Here, we develop a life history–based mutual mate choice model that takes into account the lost-opportunity costs for males from time out in sperm recovery and lets mate competition be determined by the prevailing mate choice strategies. We assume that high mating rate may potentially lead to sperm depletion in males, and that as a result, female reproduction may be limited by the availability of sperm. Increasing variation in male quality leads, in general, to increased selective mate choice by females, and vice versa. Lower-quality males may, however, gain access to more fecund higher-quality females by lowering their courting rate, thus increasing their sperm reserves. When faced with strong male competition for mates, low-quality males become less choosy, which leads to assortative mating for quality and an increased mating rate across all males. With assortative mating, the frequency of antagonistic interactions (sexual conflict) is reduced, allowing males to lower the time spent replenishing sperm reserves in order to increase mating rate. This in turn leads to lower sperm levels at mating and therefore could lead to negative effects on female fitness via sperm limitation

    Integrating personality research and animal contest theory: aggressiveness in the green swordtail <i>Xiphophorus helleri</i>

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    &lt;p&gt;Aggression occurs when individuals compete over limiting resources. While theoretical studies have long placed a strong emphasis on context-specificity of aggression, there is increasing recognition that consistent behavioural differences exist among individuals, and that aggressiveness may be an important component of individual personality. Though empirical studies tend to focus on one aspect or the other, we suggest there is merit in modelling both within-and among-individual variation in agonistic behaviour simultaneously. Here, we demonstrate how this can be achieved using multivariate linear mixed effect models. Using data from repeated mirror trials and dyadic interactions of male green swordtails, &lt;i&gt;Xiphophorus helleri&lt;/i&gt;, we show repeatable components of (co)variation in a suite of agonistic behaviour that is broadly consistent with a major axis of variation in aggressiveness. We also show that observed focal behaviour is dependent on opponent effects, which can themselves be repeatable but were more generally found to be context specific. In particular, our models show that within-individual variation in agonistic behaviour is explained, at least in part, by the relative size of a live opponent as predicted by contest theory. Finally, we suggest several additional applications of the multivariate models demonstrated here. These include testing the recently queried functional equivalence of alternative experimental approaches, (e. g., mirror trials, dyadic interaction tests) for assaying individual aggressiveness.&lt;/p&gt

    Observed shifts in the contact zone between two forms of the diving beetle Hydroporus memnonius are consistent with predictions from sexual conflict.

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    Sexual conflict drives both inter- and intrasexual dimorphisms in many diving beetles, where male persistence and female resistance traits co-evolve in an antagonistic manner. To date most studies have focussed on species where rough and smooth females and their associated males typically co-occur within populations, where phenotype matching between morphs may maintain forms as stable polymorphisms. The Palaearctic diving beetle Hydroporus memnonius is characterised by having dimorphic (rough var. castaneus and smooth, shining) females and associated males which differ in persistence traits; the two forms being largely distributed parapatrically. In this species, instead of mating trade-offs between morphs, males associated with castaneus females should have a mating advantage with both this form and shining females, due to their increased persistence abilities on either cuticular surface. This may be expected to lead to the replacement of the shining form with castaneus in areas where the two come into contact. Using data collected over a thirty year period, we show that this process of population replacement is indeed occurring, castaneus having expanded significantly at the expense of the shining female form. Whilst populations of both forms close to the contact zone appear to differ in their thermal physiology, these differences are minor and suggest that the expansion of castaneus is not linked to climatic warming in recent decades. Instead we argue that the observed spread of castaneus and its associated male may result from the dynamics of sexually antagonistic coevolution in this beetle

    Building Babies - Chapter 16

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    In contrast to birds, male mammals rarely help to raise the offspring. Of all mammals, only among rodents, carnivores, and primates, males are sometimes intensively engaged in providing infant care (Kleiman and Malcolm 1981). Male caretaking of infants has long been recognized in nonhuman primates (Itani 1959). Given that infant care behavior can have a positive effect on the infant’s development, growth, well-being, or survival, why are male mammals not more frequently involved in “building babies”? We begin the chapter defining a few relevant terms and introducing the theory and hypotheses that have historically addressed the evolution of paternal care. We then review empirical findings on male care among primate taxa, before focusing, in the final section, on our own work on paternal care in South American owl monkeys (Aotus spp.). We conclude the chapter with some suggestions for future studies.Deutsche Forschungsgemeinschaft (HU 1746/2-1) Wenner-Gren Foundation, the L.S.B. Leakey Foundation, the National Geographic Society, the National Science Foundation (BCS-0621020), the University of Pennsylvania Research Foundation, the Zoological Society of San Dieg

    Population density and group size effects on reproductive behavior in a simultaneous hermaphrodite

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    <p>Abstract</p> <p>Background</p> <p>Despite growing evidence that population dynamic processes can have substantial effects on mating system evolution, little is known about their effect on mating rates in simultaneous hermaphrodites. According to theory, mating rate is expected to increase with mate availability because mating activity is primarily controlled by the male sexual function. A different scenario appears plausible in the hermaphroditic opisthobranch <it>Chelidonura sandrana</it>. Here, field mating rates are close to the female fitness optimum, suggesting that mating activity remains unresponsive to variation in mate availability.</p> <p>Results</p> <p>Applying an experimental design that aims at independent experimental manipulation of density and social group size, we find substantial increases in mate encounter rate with both factors, but no statistically detectable effects on mating rate in <it>C. sandrana</it>. Instead, mating rate remained close to the earlier determined female fitness optimum.</p> <p>Conclusions</p> <p>We demonstrate that mating rate in <it>C. sandrana </it>is largely unresponsive to variation in mate availability and is maintained close to the female fitness optimum. These findings challenge the prevailing notion of male driven mating rates in simultaneous hermaphrodites and call for complementary investigations of mating rate effects on fitness through the male sexual function.</p

    Only females in poor condition display a clear preference and prefer males with an average badge

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    <p>Abstract</p> <p>Background</p> <p>Female condition-dependent variation in mate preference may have important evolutionary implications, not only within the same population but also among populations. There are few experiments, however, on how condition and/or genotype influences female mate preferences. The black throat patch of the male house sparrow, <it>Passer domesticus</it>, is an intensively studied plumage trait. It is often referred to as a 'badge of status' and seems to be involved in female mate choice, but differences exist among populations. Between-population variation in mate preference may occur for condition-dependent mate preferences. We tested the hypothesis that female preference may vary with female quality (body condition). Therefore, we measured female preference for badge size using an aviary two-choice test in which females were presented with two males that had different sizes of badges (enlarged or averaged).</p> <p>Results</p> <p>Overall we did not find a female preference for enlarged or average badges, but low-quality females spent more time near average badge males. Conversely, high-quality females did not show a clear preference.</p> <p>Conclusions</p> <p>Collectively, these results indicate that female preference varies with female quality. Differences in female condition are causes of within-population variation in mating preferences. To our knowledge, our results provide one of the first experimental evidences that variation in preference for a male ornament is associated with female condition. In our study, however, only females of low condition displayed a clear mate preference. Differences observed among populations could be partly explained by differences in female condition.</p
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