Understanding individual‐level variation in response to the environment is fundamental to understanding life‐history evolution and population dynamics. Telomeres, the protective caps at the ends of chromosomes, shorten in response to oxidative stress, and telomere shortening is correlated with reduced survival and life span. Investigating telomere dynamics may help us quantify individual variation in the costs experienced from social and ecological factors, and enhance our understanding of the dynamics of natural populations.Here, we study spatio‐temporal variation in lifelong telomere dynamics in the Seychelles warbler, Acrocephalus sechellensis. We combine long‐term life history and ecological data with a large longitudinal dataset of mean telomere lengths, consisting of 1,808 samples from 22 cohorts born between 1993 and 2014. We provide a detailed analysis of how telomere dynamics vary over individual life spans and cohorts, and with spatio‐temporal variation in the social and ecological environment.We found that telomere length decreases with cross‐sectional and longitudinal measures of age, and most rapidly very early in life. However, both cross‐sectional and longitudinal data suggested that against this overall pattern of shortening, bouts of telomere length increase occur in some individuals. Using a large number of repeated measurements we show statistically that these increases are unlikely to be explained solely by qPCR measurement error.Telomere length varied markedly among cohorts. Telomere length was positively associated with temporal variation in island‐wide insect abundance—a key resource for the insectivorous Seychelles warbler—suggesting that the costs associated with living in harsher environments can be studied by investigating telomere dynamics. We also found evidence for sex‐specific relationships between telomeres and tarsus length, potentially reflecting differential costs of growth.Our long‐term data show that in a natural population, telomere dynamics vary in a complex manner over individual life spans, and across space and time. Variance in telomere dynamics among individuals is the product of a wide array of genetic, parental and environmental factors. Explaining this variation more fully will require the integration of comprehensive long‐term ecological and genetic data from multiple populations and species.

This is a repository copy of Coordinated parental provisioning is related to feeding rate and reproductive success in a songbird.

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Inbreeding results in more homozygous offspring that should suffer reduced fitness, but it can be difficult to quantify these costs for several reasons. First, inbreeding depression may vary with ecological or physiological stress and only be detectable over long time periods. Second, parental homozygosity may indirectly affect offspring fitness, thus confounding analyses that consider offspring homozygosity alone. Finally, measurement of inbreeding coefficients, survival and reproductive success may often be too crude to detect inbreeding costs in wild populations. Telomere length provides a more precise measure of somatic costs, predicts survival in many species and should reflect differences in somatic condition that result from varying ability to cope with environmental stressors. We studied relative telomere length in a wild population of Seychelles warblers (Acrocephalus sechellensis) to assess the lifelong relationship between individual homozygosity, which reflects genome‐wide inbreeding in this species, and telomere length. In juveniles, individual homozygosity was negatively associated with telomere length in poor seasons. In adults, individual homozygosity was consistently negatively related to telomere length, suggesting the accumulation of inbreeding depression during life. Maternal homozygosity also negatively predicted offspring telomere length. Our results show that somatic inbreeding costs are environmentally dependent at certain life stages but may accumulate throughout life.

Lay SummaryOffspring raised with siblings often have to compete for access to limited parental resources; but in adulthood, this prior exposure to competition may be beneficial rather than costly. In Seychelles warblers, nestlings raised with competitors suffered more than those raised alone; but during adulthood, those raised with competition appeared to outperform those raised singly. These results suggest a more multifaceted link between early-life competition and lifetime performance than is currently assumed.

Providing plausible mechanisms to explain variation in the honesty of information communicated through offspring begging signals is fundamental to our understanding of parent-offspring conflict and the evolution of family life. A recently published research article used comparative analyses to investigate two long-standing hypotheses that may explain the evolution of begging behavior. The results suggested that direct competition between offspring for parental resources decreases begging honesty, whereas indirect, kin-selected benefits gained through saving parental resources for the production of future siblings increase begging honesty. However, we feel that evidence for a role of kin selection in this context is still missing. We present a combination of arguments and empirical tests to outline alternative sources of interspecific variation in offspring begging levels and discuss avenues for further research that can bring us closer to a complete understanding of the evolution of offspring signaling. K E Y W O R D S :Comparative studies, competition, kin selection, signaling.

Parents who raise their nestling in a communal nest alongside the nestling of other parents can reduce costly competition between offspring by providing more food. In the Seychelles warbler, we show that nestlings raised with a sibling have lower mass and survival than those raised alone, whereas nestlings raised with a nonsibling do not suffer these costs. Our results suggest that increased food provisioning can reduce competition among nonsiblings and facilitate the evolution of joint-nesting.

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