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Interbirth intervals: Intrafamilial, intragenomic and intrasomatic conflict

Background and objectives: Interbirth intervals (IBIs) mediate a trade-off between child number and child survival. Life history theory predicts that the evolutionarily optimal IBI differs for different individuals whose fitness is affected by how closely a mother spaces her children. The objective...

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Autor principal: Haig, David
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3917425/
https://www.ncbi.nlm.nih.gov/pubmed/24480612
http://dx.doi.org/10.1093/emph/eou002
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author Haig, David
author_facet Haig, David
author_sort Haig, David
collection PubMed
description Background and objectives: Interbirth intervals (IBIs) mediate a trade-off between child number and child survival. Life history theory predicts that the evolutionarily optimal IBI differs for different individuals whose fitness is affected by how closely a mother spaces her children. The objective of the article is to clarify these conflicts and explore their implications for public health. Methodology: Simple models of inclusive fitness and kin conflict address the evolution of human birth-spacing. Results: Genes of infants generally favor longer intervals than genes of mothers, and infant genes of paternal origin generally favor longer IBIs than genes of maternal origin. Conclusions and implications: The colonization of maternal bodies by offspring cells (fetal microchimerism) raises the possibility that cells of older offspring could extend IBIs by interfering with the implantation of subsequent embryos.
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spelling pubmed-39174252014-02-07 Interbirth intervals: Intrafamilial, intragenomic and intrasomatic conflict Haig, David Evol Med Public Health Original Research Article Background and objectives: Interbirth intervals (IBIs) mediate a trade-off between child number and child survival. Life history theory predicts that the evolutionarily optimal IBI differs for different individuals whose fitness is affected by how closely a mother spaces her children. The objective of the article is to clarify these conflicts and explore their implications for public health. Methodology: Simple models of inclusive fitness and kin conflict address the evolution of human birth-spacing. Results: Genes of infants generally favor longer intervals than genes of mothers, and infant genes of paternal origin generally favor longer IBIs than genes of maternal origin. Conclusions and implications: The colonization of maternal bodies by offspring cells (fetal microchimerism) raises the possibility that cells of older offspring could extend IBIs by interfering with the implantation of subsequent embryos. Oxford University Press 2014-02-07 /pmc/articles/PMC3917425/ /pubmed/24480612 http://dx.doi.org/10.1093/emph/eou002 Text en © The Author(s) 2014. Published by Oxford University Press on behalf of the Foundation for Evolution, Medicine, and Public Health. http://creativecommons.org/licenses/by/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Research Article
Haig, David
Interbirth intervals: Intrafamilial, intragenomic and intrasomatic conflict
title Interbirth intervals: Intrafamilial, intragenomic and intrasomatic conflict
title_full Interbirth intervals: Intrafamilial, intragenomic and intrasomatic conflict
title_fullStr Interbirth intervals: Intrafamilial, intragenomic and intrasomatic conflict
title_full_unstemmed Interbirth intervals: Intrafamilial, intragenomic and intrasomatic conflict
title_short Interbirth intervals: Intrafamilial, intragenomic and intrasomatic conflict
title_sort interbirth intervals: intrafamilial, intragenomic and intrasomatic conflict
topic Original Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3917425/
https://www.ncbi.nlm.nih.gov/pubmed/24480612
http://dx.doi.org/10.1093/emph/eou002
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