Cargando…
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...
Autores principales: | , , , , |
---|---|
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 |
_version_ | 1785054763986976768 |
---|---|
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. |
format | Online Article Text |
id | pubmed-10244968 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | The Royal Society |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT brindlematilda theevolutionofmasturbationisassociatedwithpostcopulatoryselectionandpathogenavoidanceinprimates AT fergusongowhenry theevolutionofmasturbationisassociatedwithpostcopulatoryselectionandpathogenavoidanceinprimates AT williamsonjoseph theevolutionofmasturbationisassociatedwithpostcopulatoryselectionandpathogenavoidanceinprimates AT thomsenruth theevolutionofmasturbationisassociatedwithpostcopulatoryselectionandpathogenavoidanceinprimates AT sommervolker theevolutionofmasturbationisassociatedwithpostcopulatoryselectionandpathogenavoidanceinprimates AT brindlematilda evolutionofmasturbationisassociatedwithpostcopulatoryselectionandpathogenavoidanceinprimates AT fergusongowhenry evolutionofmasturbationisassociatedwithpostcopulatoryselectionandpathogenavoidanceinprimates AT williamsonjoseph evolutionofmasturbationisassociatedwithpostcopulatoryselectionandpathogenavoidanceinprimates AT thomsenruth evolutionofmasturbationisassociatedwithpostcopulatoryselectionandpathogenavoidanceinprimates AT sommervolker evolutionofmasturbationisassociatedwithpostcopulatoryselectionandpathogenavoidanceinprimates |