A gene–culture co-evolutionary perspective on the puzzle of human twinship

Natural selection should favour litter sizes that optimise trade-offs between brood-size and offspring viability. Across the primate order, the modal litter size is one, suggesting a deep history of selection favouring minimal litters in primates. Humans, however – despite having the longest juvenil...

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Main Authors: Augusto Dalla Ragione, Cody T. Ross, Daniel Redhead
Format: Article
Language:English
Published: Cambridge University Press 2024-01-01
Series:Evolutionary Human Sciences
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Online Access:https://www.cambridge.org/core/product/identifier/S2513843X24000306/type/journal_article
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author Augusto Dalla Ragione
Cody T. Ross
Daniel Redhead
author_facet Augusto Dalla Ragione
Cody T. Ross
Daniel Redhead
author_sort Augusto Dalla Ragione
collection DOAJ
description Natural selection should favour litter sizes that optimise trade-offs between brood-size and offspring viability. Across the primate order, the modal litter size is one, suggesting a deep history of selection favouring minimal litters in primates. Humans, however – despite having the longest juvenile period and slowest life-history of all primates – still produce twin births at appreciable rates, even though such births are costly. This presents an evolutionary puzzle. Why is twinning still expressed in humans despite its cost? More puzzling still is the discordance between the principal explanations for human twinning and extant empirical data. Such explanations propose that twinning is regulated by phenotypic plasticity in polyovulation, permitting the production of larger sib sets if and when resources are abundant. However, comparative data suggest that twinning rates are actually highest in poorer economies and lowest in richer, more developed economies. We propose that a historical dynamic of gene–culture co-evolution might better explain this geographic patterning. Our explanation distinguishes geminophilous and geminophobic cultural contexts, as those celebrating twins (e.g. through material support) and those hostile to twins (e.g. through sanction of twin-infanticide). Geminophilous institutions, in particular, may buffer the fitness cost associated with twinning, potentially reducing selection pressures against polyovulation. We conclude by synthesising a mathematical and empirical research programme that might test our ideas.
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spelling doaj-art-8b8aa4c38a0f4e00886bde663e70cc902025-08-20T02:13:48ZengCambridge University PressEvolutionary Human Sciences2513-843X2024-01-01610.1017/ehs.2024.30A gene–culture co-evolutionary perspective on the puzzle of human twinshipAugusto Dalla Ragione0https://orcid.org/0009-0008-4472-4242Cody T. Ross1https://orcid.org/0000-0002-0067-4799Daniel Redhead2https://orcid.org/0000-0002-2809-8121Department of Human Behavior, Ecology and Culture, Max Planck Institute for Evolutionary Anthropology, Leipzig, GermanyDepartment of Human Behavior, Ecology and Culture, Max Planck Institute for Evolutionary Anthropology, Leipzig, GermanyDepartment of Human Behavior, Ecology and Culture, Max Planck Institute for Evolutionary Anthropology, Leipzig, Germany Department of Sociology, University of Groningen, Grote Rozenstraat 31, 9712 TG Groningen, The Netherlands Inter-University Center for Social Science Theory and Methodology, University of Groningen, Groningen, The NetherlandsNatural selection should favour litter sizes that optimise trade-offs between brood-size and offspring viability. Across the primate order, the modal litter size is one, suggesting a deep history of selection favouring minimal litters in primates. Humans, however – despite having the longest juvenile period and slowest life-history of all primates – still produce twin births at appreciable rates, even though such births are costly. This presents an evolutionary puzzle. Why is twinning still expressed in humans despite its cost? More puzzling still is the discordance between the principal explanations for human twinning and extant empirical data. Such explanations propose that twinning is regulated by phenotypic plasticity in polyovulation, permitting the production of larger sib sets if and when resources are abundant. However, comparative data suggest that twinning rates are actually highest in poorer economies and lowest in richer, more developed economies. We propose that a historical dynamic of gene–culture co-evolution might better explain this geographic patterning. Our explanation distinguishes geminophilous and geminophobic cultural contexts, as those celebrating twins (e.g. through material support) and those hostile to twins (e.g. through sanction of twin-infanticide). Geminophilous institutions, in particular, may buffer the fitness cost associated with twinning, potentially reducing selection pressures against polyovulation. We conclude by synthesising a mathematical and empirical research programme that might test our ideas.https://www.cambridge.org/core/product/identifier/S2513843X24000306/type/journal_articleTwinshipcoevolutiontwinsgeminophiliageminophobia
spellingShingle Augusto Dalla Ragione
Cody T. Ross
Daniel Redhead
A gene–culture co-evolutionary perspective on the puzzle of human twinship
Evolutionary Human Sciences
Twinship
coevolution
twins
geminophilia
geminophobia
title A gene–culture co-evolutionary perspective on the puzzle of human twinship
title_full A gene–culture co-evolutionary perspective on the puzzle of human twinship
title_fullStr A gene–culture co-evolutionary perspective on the puzzle of human twinship
title_full_unstemmed A gene–culture co-evolutionary perspective on the puzzle of human twinship
title_short A gene–culture co-evolutionary perspective on the puzzle of human twinship
title_sort gene culture co evolutionary perspective on the puzzle of human twinship
topic Twinship
coevolution
twins
geminophilia
geminophobia
url https://www.cambridge.org/core/product/identifier/S2513843X24000306/type/journal_article
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