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Accelerated reproduction is not an adaptive response to early-life adversity in wild baboons

In humans and other long-lived species, harsh conditions in early life often lead to profound differences in adult life expectancy. In response, natural selection is expected to accelerate the timing and pace of reproduction in individuals who experience some forms of early-life adversity. However,...

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Autores principales: Weibel, Chelsea J., Tung, Jenny, Alberts, Susan C., Archie, Elizabeth A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: National Academy of Sciences 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7547275/
https://www.ncbi.nlm.nih.gov/pubmed/32958642
http://dx.doi.org/10.1073/pnas.2004018117
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author Weibel, Chelsea J.
Tung, Jenny
Alberts, Susan C.
Archie, Elizabeth A.
author_facet Weibel, Chelsea J.
Tung, Jenny
Alberts, Susan C.
Archie, Elizabeth A.
author_sort Weibel, Chelsea J.
collection PubMed
description In humans and other long-lived species, harsh conditions in early life often lead to profound differences in adult life expectancy. In response, natural selection is expected to accelerate the timing and pace of reproduction in individuals who experience some forms of early-life adversity. However, the adaptive benefits of reproductive acceleration following early adversity remain untested. Here, we test a recent version of this theory, the internal predictive adaptive response (iPAR) model, by assessing whether accelerating reproduction following early-life adversity leads to higher lifetime reproductive success. We do so by leveraging 48 y of continuous, individual-based data from wild female baboons in the Amboseli ecosystem in Kenya, including prospective, longitudinal data on multiple sources of nutritional and psychosocial adversity in early life; reproductive pace; and lifetime reproductive success. We find that while early-life adversity led to dramatically shorter lifespans, individuals who experienced early adversity did not accelerate their reproduction compared with those who did not experience early adversity. Further, while accelerated reproduction predicted increased lifetime reproductive success overall, these benefits were not specific to females who experienced early-life adversity. Instead, females only benefited from reproductive acceleration if they also led long lives. Our results call into question the theory that accelerated reproduction is an adaptive response to both nutritional and psychosocial sources of early-life adversity in baboons and other long-lived species.
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spelling pubmed-75472752020-10-22 Accelerated reproduction is not an adaptive response to early-life adversity in wild baboons Weibel, Chelsea J. Tung, Jenny Alberts, Susan C. Archie, Elizabeth A. Proc Natl Acad Sci U S A Biological Sciences In humans and other long-lived species, harsh conditions in early life often lead to profound differences in adult life expectancy. In response, natural selection is expected to accelerate the timing and pace of reproduction in individuals who experience some forms of early-life adversity. However, the adaptive benefits of reproductive acceleration following early adversity remain untested. Here, we test a recent version of this theory, the internal predictive adaptive response (iPAR) model, by assessing whether accelerating reproduction following early-life adversity leads to higher lifetime reproductive success. We do so by leveraging 48 y of continuous, individual-based data from wild female baboons in the Amboseli ecosystem in Kenya, including prospective, longitudinal data on multiple sources of nutritional and psychosocial adversity in early life; reproductive pace; and lifetime reproductive success. We find that while early-life adversity led to dramatically shorter lifespans, individuals who experienced early adversity did not accelerate their reproduction compared with those who did not experience early adversity. Further, while accelerated reproduction predicted increased lifetime reproductive success overall, these benefits were not specific to females who experienced early-life adversity. Instead, females only benefited from reproductive acceleration if they also led long lives. Our results call into question the theory that accelerated reproduction is an adaptive response to both nutritional and psychosocial sources of early-life adversity in baboons and other long-lived species. National Academy of Sciences 2020-10-06 2020-09-21 /pmc/articles/PMC7547275/ /pubmed/32958642 http://dx.doi.org/10.1073/pnas.2004018117 Text en Copyright © 2020 the Author(s). Published by PNAS. https://creativecommons.org/licenses/by-nc-nd/4.0/ https://creativecommons.org/licenses/by-nc-nd/4.0/This open access article is distributed under Creative Commons Attribution-NonCommercial-NoDerivatives License 4.0 (CC BY-NC-ND) (https://creativecommons.org/licenses/by-nc-nd/4.0/) .
spellingShingle Biological Sciences
Weibel, Chelsea J.
Tung, Jenny
Alberts, Susan C.
Archie, Elizabeth A.
Accelerated reproduction is not an adaptive response to early-life adversity in wild baboons
title Accelerated reproduction is not an adaptive response to early-life adversity in wild baboons
title_full Accelerated reproduction is not an adaptive response to early-life adversity in wild baboons
title_fullStr Accelerated reproduction is not an adaptive response to early-life adversity in wild baboons
title_full_unstemmed Accelerated reproduction is not an adaptive response to early-life adversity in wild baboons
title_short Accelerated reproduction is not an adaptive response to early-life adversity in wild baboons
title_sort accelerated reproduction is not an adaptive response to early-life adversity in wild baboons
topic Biological Sciences
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7547275/
https://www.ncbi.nlm.nih.gov/pubmed/32958642
http://dx.doi.org/10.1073/pnas.2004018117
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