ArticleThe Journal of animal ecology2020
Experimentally increased brood size accelerates actuarial senescence and increases subsequent reproductive effort in a wild bird population.
Article in The Journal of animal ecology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.
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Who cites it
11 citing papers in PubMed, 31 citations in OpenAlex.
- Reproductive Drivers of Temporal Telomere Dynamics in Female Tree Swallows.Molecular ecology · 2026Article
- Flexibility of exercise capacity during nestling feeding in blue tits.The Journal of experimental biology · 2026Article
- Reproductive aging and age-dependent parental effects on offspring in a long-lived seabird.Oecologia · 2026Article
- No Evidence That Life History Strategies Shape Within-Body Mosaics of Ageing.Molecular ecology · 2025Article
- Experimentally manipulated food availability affects offspring quality but not quantity in zebra finch meso-populations.Oecologia · 2022Article
- Telomere dynamics in female Columbian ground squirrels: recovery after emergence and loss after reproduction.Oecologia · 2022Article
- The stagnation paradox: the ever-improving but (more or less) stationary population fitness.Proceedings. Biological sciences · 2021Review
- Beneficial cumulative effects of old parental age on offspring fitness.Proceedings. Biological sciences · 2021Article
- The influence of phylogeny and life history on telomere lengths and telomere rate of change among bird species: A meta-analysis.Ecology and evolution · 2021Review
- Predation has small, short-term, and in certain conditions random effects on the evolution of aging.BMC ecology and evolution · 2021Article
- Experimentally increased brood size accelerates actuarial senescence and increases subsequent reproductive effort in a wild bird population.The Journal of animal ecology · 2020Article
Corrections and comments
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Authors and funding
3 authors at 1 institution in 2 countries.
Funding
No grant is acknowledged in the PubMed record.
Abstract
The assumption that reproductive effort decreases somatic state, accelerating ageing, is central to our understanding of life-history variation. Maximal reproductive effort early in life is predicted to be maladaptive by accelerating ageing disproportionally, decreasing fitness. Optimality theory predicts that reproductive effort is restrained early in life to balance the fitness contribution of reproduction against the survival cost induced by the reproductive effort. When adaptive, the level of reproductive restraint is predicted to be inversely linked to the remaining life expectancy, potentially resulting in a terminal effort in the last period of reproduction. Experimental tests of the reproductive restraint hypothesis require manipulation of somatic state and subsequent investigation of reproductive effort and residual life span. To our knowledge the available evidence remains inconclusive, and hence reproductive restraint remains to be demonstrated. We modulated somatic state through a lifelong brood size manipulation in wild jackdaws and measured its consequences for age-dependent mortality and reproductive success. The assumption that lifelong increased brood size reduced somatic state was supported: Birds rearing enlarged broods showed subsequent increased rate of actuarial senescence, resulting in reduced residual life span. The treatment induced a reproductive response in later seasons: Egg volume and nestling survival were higher in subsequent seasons in the increased versus reduced broods' treatment group. We detected these increases in egg volume and nestling survival despite the expectation that in the absence of a change in reproductive effort, the reduced somatic state indicated by the increased mortality rate would result in lower reproductive output. This leads us to conclude that the higher reproductive success we observed was the result of higher reproductive effort. Our findings show that reproductive effort negatively covaries with remaining life expectancy, supporting optimality theory and confirming reproductive restraint as a key factor underpinning life-history variation.
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