Helen L. Osmond

Swingin' in the rain: condition dependence and sexual selection in a capricious world.

Signals used in mate attraction are predicted to be highly condition dependent, and thus should be sensitive to environmental contributions to condition. However, the effects of temporal fluctuations in the environment on sexual selection in long-lived animals have been largely ignored. Female superb fairy-wrens, Malurus cyaneus, use the time that males moult into nuptial plumage prior to the onset of the breeding season to distinguish between the extra-group sires that dominate paternity. Although moult varies predictably with age, and shows marked differences between males, the phenotypic distribution also changes radically with climate; so after dry summers few males can attempt early moult. We use the recently introduced de-lifing technique to examine sexual selection gradients over 15 years of selection. Overall, there was strong evidence of directional sexual selection for early moult. However, sexual selection was much stronger when the conditions were favourable (rainfall was high), and selection was undetectable in some years. The contribution of early moulting males to population growth increased when many males moulted early, decreased when early moulting males suffered disproportionate mortality and decreased when females lacked subordinate helpers, forcing them to cede paternity to their social partner. These data suggest that short-term and laboratory studies of mate choice and sexual selection may misrepresent or underestimate the complexity of the sexual selection landscape.

Can we measure the benefits of help in cooperatively breeding birds: the case of superb fairy-wrens Malurus cyaneus ?

1. Correlational studies of reproductive success are plagued by difficulty over the direction of causation. For example, improved reproductive success with age can result from increased experience or reproductive effort, or selection against low-quality phenotypes that survive poorly. An association between supernumeraries and reproductive success in cooperative breeders can arise either because supernumeraries boost productivity, or productive territories accumulate supernumeraries. 2. Paired comparisons of parents sampled with and without supernumeraries have recently been widely applied to quantify help. However, Dickinson & Hatchwell (2004) have argued that this approach is flawed. They conjectured that those groups that gain supernumeraries are a biased superior sample of those that initially lack supernumeraries, while groups that lose supernumeraries will be a sample of inferior cooperative groups. They predict that these biased comparisons will underestimate the effect of help. 3. This conjecture has neither been explored theoretically, nor empirically tested. We use data from a 19-year study of the superb fairy-wren Malurus cyaneus to examine the conjecture and derive predictors of annual reproductive success in this species. 4. We introduce statistical models of reproductive success based on a zero-inflated Poisson link function to identify three strong correlates of reproductive success: high spring rainfall, progress from the first to later years of life, and acquisition of supernumeraries. 5. First year females that died after breeding and those that survived to breed again had similar productivity. As female productivity improves with age, increased reproductive skill or effort is implicated rather than selection against inferior phenotypes. 6. We argue that the Dickinson-Hatchwell conjecture does not constrain paired comparisons in M. cyaneus. The dominant male and breeding female gain no immediate fecundity advantage from supernumeraries. 7. Effects on the future survival of dominants are even more difficult, as while helpers could enhance survival of dominants, a territory that facilitates survival should also accumulate philopatric supernumeraries. Males, the philopatric sex, did not survive better on territories with supernumeraries. However, females, the dispersive sex, had higher survival as the number of supernumeraries increased, because helpers allowed them to reduce the costs of reproduction. These data exacerbate the paradox posed by previously reported costs that supernumeraries impose on dominant males.

Increased Opportunities for Cuckoldry may be Why Dominant Male Fairy-Wrens Tolerate Helpers

The highest known rates of extra-pair fertilization (76%) occur in the superb fairy-wren (Malurus cyaneus), a bird that lives in both breeding pairs and in cooperative groups where 2-5 males assist a single female. Males living in groups are cuckolded more often than males in pairs, apparently because females can rely on helpers as an alternative source of care, and so do not need to allow their mate fertilizations. It is therefore unclear why dominant males tolerate helpers. Here we show that dominant males with helpers provide less parental care during the nestling period, and use this reduced workload to make extra-territorial forays which are used to court extra-group females. DNA fingerprinting suggests that this increased display rate provides them with an advantage in obtaining extra-group copulations. These data suggest that within-pair and extra-pair paternity will not always be positively correlated.

Display rate by male fairy-wrens (Malurus cyaneus) during the fertile period of females has little influence on extra-pair mate choice

Abstract Empirical and theoretical studies have only recently begun to examine how females use complex multi-component displays when selecting mates. Superb fairy-wrens are well suited to the study of female choice because females have control over extra-group paternity and cuckold their mates at high rates, while males possess a variety of sexually selected traits. Available evidence suggests that females base their extra-group mate choice on the timing of male moult into breeding plumage or the onset of display. However, males continue to perform elaborate displays throughout the season, and direct most displays to females during their fertile period. We therefore conducted focal observations on fertile females to quantify the frequency of male display and used microsatellite genotyping to compare the role of display rate during the breeding season and the timing of male moult on female mate choice. We show that the addition of data on male display rate does not improve our ability to predict which males obtain extra-group paternity. The timing of male moult into breeding plumage remains the only predictor of male extra-group reproductive success. Nevertheless, we found that males displayed more to females that were unable to select extra-group mates on the basis of the timing of moult or the onset of display. This raises the possibility that there are circumstances when females use display rate to discriminate between potential extra-group sires. Overall this study supports the theoretical prediction that females are more likely to base their mate choice on reliable indicators of male quality such as fixed morphological traits and displays of endurance, in this case an early moult into breeding plumage and the performance of an elaborate display during the winter, than a flexible behavioural trait such as display rate during the breeding season.

Fluctuations in population composition dampen the impact of phenotypic plasticity on trait dynamics in superb fairy‐wrens

1. In structured populations, phenotypic change can result from changes throughout an individuals lifetime (phenotypic plasticity, age-related changes), selection and changes in population composition (environment- or density-driven fluctuations in age-structure). 2. The contribution of population dynamics to phenotypic change has often been ignored. However, for understanding trait dynamics, it is important to identify both the individual- and population-level mechanisms responsible for trait change, because they potentially reinforce or counteract each other. 3. We use 22 years of field data to investigate the dynamics of a sexually selected phenological trait, the timing of nuptial moult in superb fairy-wrens Malurus cyaneus. 4. We show that trait expression is both climate- and age-dependent, but that phenotypic plasticity in response to climate variability also varies with age. Old males can acquire nuptial plumage very early after high rainfall, but 1- to 2-year-olds cannot. However, males of all ages that defer moult to later in the year acquire nuptial plumage earlier when conditions are warmer. 5. The underlying mechanism appears to be that old males may risk moulting in the most challenging period of the year: in autumn, when drought restricts food abundance and during the cold winter. By contrast, young males always moult during the spring transition to benign - warmer and generally wetter - conditions. Temperature changes dominate this transition that heralds the breeding season, thereby causing both young and late-moulting older birds to be temperature sensitive. 6. Climate and age also affect trait dynamics via a population dynamical pathway. The same high rainfall that triggers early moulting in old males concurrently increases offspring recruitment and thereby reduces the average age of males in the population. Consequently, effects of rainfall on trait dynamics through phenotypic plasticity of old males are dampened by synchronous rejuvenation of the age-structure. 7. A long-term trend towards drier environments prompted phenotypic change because of plasticity, but this was masked by climate-driven demographic change (causing apparent stasis). This suggests a novel explanation for why trait change may fail to reflect the observed pattern of directional selection or phenotypic plasticity.

Inbreeding, inbreeding depression, and infidelity in a cooperatively breeding bird*: INBREEDING AND INFIDELITY

Inbreeding depression plays a major role in shaping mating systems: in particular, inbreeding avoidance is often proposed as a mechanism explaining extra‐pair reproduction in socially monogamous species. This suggestion relies on assumptions that are rarely comprehensively tested: that inbreeding depression is present, that higher kinship between social partners increases infidelity, and that infidelity reduces the frequency of inbreeding. Here, we test these assumptions using 26 years of data for a cooperatively breeding, socially monogamous bird with high female infidelity, the superb fairy‐wren (Malurus cyaneus). Although inbred individuals were rare (∼6% of offspring), we found evidence of inbreeding depression in nestling mass (but not in fledgling survival). Mother–son social pairings resulted in 100% infidelity, but kinship between a social pair did not otherwise predict female infidelity. Nevertheless, extra‐pair offspring were less likely to be inbred than within‐pair offspring. Finally, the social environment (the number of helpers in a group) did not affect offspring inbreeding coefficients or inbreeding depression levels. In conclusion, despite some agreement with the assumptions that are necessary for inbreeding avoidance to drive infidelity, the apparent scarcity of inbreeding events and the observed levels of inbreeding depression seem insufficient to explain the ubiquitous infidelity in this system, beyond the mother–son mating avoidance.