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The evolution of masturbation is associated with postcopulatory selection and pathogen avoidance in primates

Masturbation occurs throughout the animal kingdom. At first glance, however, the fitness benefits of this self-directed behaviour are unclear. Regardless, several drivers have been proposed. Non-functional hypotheses posit that masturbation is either a pathology, or a byproduct of high underlying se...

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Autores principales: Brindle, Matilda, Ferguson-Gow, Henry, Williamson, Joseph, Thomsen, Ruth, Sommer, Volker
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10244968/
https://www.ncbi.nlm.nih.gov/pubmed/37282530
http://dx.doi.org/10.1098/rspb.2023.0061
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author Brindle, Matilda
Ferguson-Gow, Henry
Williamson, Joseph
Thomsen, Ruth
Sommer, Volker
author_facet Brindle, Matilda
Ferguson-Gow, Henry
Williamson, Joseph
Thomsen, Ruth
Sommer, Volker
author_sort Brindle, Matilda
collection PubMed
description Masturbation occurs throughout the animal kingdom. At first glance, however, the fitness benefits of this self-directed behaviour are unclear. Regardless, several drivers have been proposed. Non-functional hypotheses posit that masturbation is either a pathology, or a byproduct of high underlying sexual arousal, whereas functional hypotheses argue an adaptive benefit. The Postcopulatory Selection Hypothesis states that masturbation aids the chances of fertilization, while the Pathogen Avoidance Hypothesis states that masturbation helps reduce host infection by flushing pathogens from the genital tract. Here, we present comprehensive new data documenting masturbation across the primate order and use these, in conjunction with phylogenetic comparative methods, to reconstruct the evolutionary pathways and correlates of masturbation. We find that masturbation is an ancient trait within the primate order, becoming a more common aspect of the haplorrhine behavioural repertoire after the split from tarsiers. Our analyses provide support for both the Postcopulatory Selection and Pathogen Avoidance Hypotheses in male primates, suggesting that masturbation may be an adaptive trait, functioning at a macroevolutionary scale.
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spelling pubmed-102449682023-06-08 The evolution of masturbation is associated with postcopulatory selection and pathogen avoidance in primates Brindle, Matilda Ferguson-Gow, Henry Williamson, Joseph Thomsen, Ruth Sommer, Volker Proc Biol Sci Evolution Masturbation occurs throughout the animal kingdom. At first glance, however, the fitness benefits of this self-directed behaviour are unclear. Regardless, several drivers have been proposed. Non-functional hypotheses posit that masturbation is either a pathology, or a byproduct of high underlying sexual arousal, whereas functional hypotheses argue an adaptive benefit. The Postcopulatory Selection Hypothesis states that masturbation aids the chances of fertilization, while the Pathogen Avoidance Hypothesis states that masturbation helps reduce host infection by flushing pathogens from the genital tract. Here, we present comprehensive new data documenting masturbation across the primate order and use these, in conjunction with phylogenetic comparative methods, to reconstruct the evolutionary pathways and correlates of masturbation. We find that masturbation is an ancient trait within the primate order, becoming a more common aspect of the haplorrhine behavioural repertoire after the split from tarsiers. Our analyses provide support for both the Postcopulatory Selection and Pathogen Avoidance Hypotheses in male primates, suggesting that masturbation may be an adaptive trait, functioning at a macroevolutionary scale. The Royal Society 2023-06-14 2023-06-07 /pmc/articles/PMC10244968/ /pubmed/37282530 http://dx.doi.org/10.1098/rspb.2023.0061 Text en © 2023 The Authors. https://creativecommons.org/licenses/by/4.0/Published by the Royal Society under the terms of the Creative Commons Attribution License http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, provided the original author and source are credited.
spellingShingle Evolution
Brindle, Matilda
Ferguson-Gow, Henry
Williamson, Joseph
Thomsen, Ruth
Sommer, Volker
The evolution of masturbation is associated with postcopulatory selection and pathogen avoidance in primates
title The evolution of masturbation is associated with postcopulatory selection and pathogen avoidance in primates
title_full The evolution of masturbation is associated with postcopulatory selection and pathogen avoidance in primates
title_fullStr The evolution of masturbation is associated with postcopulatory selection and pathogen avoidance in primates
title_full_unstemmed The evolution of masturbation is associated with postcopulatory selection and pathogen avoidance in primates
title_short The evolution of masturbation is associated with postcopulatory selection and pathogen avoidance in primates
title_sort evolution of masturbation is associated with postcopulatory selection and pathogen avoidance in primates
topic Evolution
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10244968/
https://www.ncbi.nlm.nih.gov/pubmed/37282530
http://dx.doi.org/10.1098/rspb.2023.0061
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