Abstract

Attempts to understand the causes of variation in senescence trajectories would benefit greatly from biomarkers that reflect the progressive declines in somatic integrity (SI) that lead to senescence. While telomere length has attracted considerable interest in this regard, sources of variation in telomere length potentially unrelated to declines in SI could, in some contexts, leave telomere attrition rates a more effective biomarker than telomere length alone. Here, we investigate whether telomere length and telomere attrition rates predict the survival of wild white‐browed sparrow‐weaver nestlings (Plocepasser mahali). Our analyses of telomere length reveal counterintuitive patterns: telomere length soon after hatching negatively predicted nestling survival to fledging, a pattern that appears to be driven by differentially high in‐nest predation of broods with longer telomeres. Telomere length did not predict survival outside this period: neither hatchling telomere length nor telomere length in the mid‐nestling period predicted survival from fledging to adulthood. Our analyses using within‐individual telomere attrition rates, by contrast, revealed the expected relationships: nestlings that experienced a higher rate of telomere attrition were less likely to survive to adulthood, regardless of their initial telomere length and independent of effects of body mass. Our findings support the growing use of telomeric traits as biomarkers of SI, but lend strength to the view that longitudinal assessments of within‐individual telomere attrition since early life may be a more effective biomarker in some contexts than telomere length alone.

Highlights

  • Senescence, the progressive late‐life decline in reproductive suc‐ cess or survival widely documented across taxa, is thought to arise from age‐related declines in Somatic Integrity (SI; the extent to which somatic tissues are free from biomolecular errors and damage; Kirkwood, 1977; Kirkwood & Holliday, 1979)

  • Survival and lifespan) both in early life and adulthood, findings con‐ sistent with it serving as a biomarker of somatic in‐ tegrity (SI), given the expectation that deficits in SI accumulate over the life course (Kirkwood, 1977) and could reduce survival at any life stage by compromising resilience to environmental hazards

  • Positive associations between telomere length and survival are far from universal (S1), and a recent meta‐analysis con‐ cluded that while a significant positive association does exist across studies, the overall effect size is small and exhibits significant heterogeneity across studies (Wilbourn et al, 2018)

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Summary

| INTRODUCTION

Senescence, the progressive late‐life decline in reproductive suc‐ cess or survival widely documented across taxa, is thought to arise from age‐related declines in Somatic Integrity (SI; the extent to which somatic tissues are free from biomolecular errors and damage; Kirkwood, 1977; Kirkwood & Holliday, 1979). Viewing telomere attrition in early life as a biomarker of within‐individual declines in SI, we predict that nest‐ lings that show higher rates of telomere attrition will have reduced downstream survival even after controlling for variation in body mass. Whether such a relationship between telomere attrition and survival gives rise to a positive association between telomere length and downstream survival will depend in part upon the extent to which variation in telomere length at the focal time points arises from mech‐ anisms other than within‐individual declines in SI. If variation in both SI and telomere length principally arises from developmental differences at the egg stage, telomere length at 4 days of age could be a stronger predictor of downstream survival than subsequent telo‐ mere attrition

| METHODS
| DISCUSSION
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