Cargando…
You Mate, I Mate: Macaque Females Synchronize Sex not Cycles
Extended female sexuality in species living in multimale-multifemale groups appears to enhance benefits from multiple males. Mating with many males, however, requires a low female monopolizability, which is affected by the spatiotemporal distribution of receptive females. Ovarian cycle synchrony pot...
Autores principales: | , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2011
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3192140/ https://www.ncbi.nlm.nih.gov/pubmed/22022541 http://dx.doi.org/10.1371/journal.pone.0026144 |
_version_ | 1782213718443032576 |
---|---|
author | Fürtbauer, Ines Mundry, Roger Heistermann, Michael Schülke, Oliver Ostner, Julia |
author_facet | Fürtbauer, Ines Mundry, Roger Heistermann, Michael Schülke, Oliver Ostner, Julia |
author_sort | Fürtbauer, Ines |
collection | PubMed |
description | Extended female sexuality in species living in multimale-multifemale groups appears to enhance benefits from multiple males. Mating with many males, however, requires a low female monopolizability, which is affected by the spatiotemporal distribution of receptive females. Ovarian cycle synchrony potentially promotes overlapping receptivity if fertile and receptive periods are tightly linked. In primates, however, mating is often decoupled from hormonal control, hence reducing the need for synchronizing ovarian events. Here, we test the alternative hypothesis that females behaviorally coordinate their receptivity while simultaneously investigating ovarian cycle synchrony in wild, seasonal Assamese macaques (Macaca assamensis), a promiscuous species with extremely extended female sexuality. Using fecal hormone analysis to assess ovarian activity we show that fertile phases are randomly distributed, and that dyadic spatial proximity does not affect their distribution. We present evidence for mating synchrony, i.e., the occurrence of the females' receptivity was significantly associated with the proportion of other females mating on a given day. Our results suggest social facilitation of mating synchrony, which explains (i) the high number of simultaneously receptive females, and (ii) the low male mating skew in this species. Active mating synchronization may serve to enhance the benefits of extended female sexuality, and may proximately explain its patterning and maintenance. |
format | Online Article Text |
id | pubmed-3192140 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-31921402011-10-21 You Mate, I Mate: Macaque Females Synchronize Sex not Cycles Fürtbauer, Ines Mundry, Roger Heistermann, Michael Schülke, Oliver Ostner, Julia PLoS One Research Article Extended female sexuality in species living in multimale-multifemale groups appears to enhance benefits from multiple males. Mating with many males, however, requires a low female monopolizability, which is affected by the spatiotemporal distribution of receptive females. Ovarian cycle synchrony potentially promotes overlapping receptivity if fertile and receptive periods are tightly linked. In primates, however, mating is often decoupled from hormonal control, hence reducing the need for synchronizing ovarian events. Here, we test the alternative hypothesis that females behaviorally coordinate their receptivity while simultaneously investigating ovarian cycle synchrony in wild, seasonal Assamese macaques (Macaca assamensis), a promiscuous species with extremely extended female sexuality. Using fecal hormone analysis to assess ovarian activity we show that fertile phases are randomly distributed, and that dyadic spatial proximity does not affect their distribution. We present evidence for mating synchrony, i.e., the occurrence of the females' receptivity was significantly associated with the proportion of other females mating on a given day. Our results suggest social facilitation of mating synchrony, which explains (i) the high number of simultaneously receptive females, and (ii) the low male mating skew in this species. Active mating synchronization may serve to enhance the benefits of extended female sexuality, and may proximately explain its patterning and maintenance. Public Library of Science 2011-10-12 /pmc/articles/PMC3192140/ /pubmed/22022541 http://dx.doi.org/10.1371/journal.pone.0026144 Text en Fürtbauer et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Fürtbauer, Ines Mundry, Roger Heistermann, Michael Schülke, Oliver Ostner, Julia You Mate, I Mate: Macaque Females Synchronize Sex not Cycles |
title | You Mate, I Mate: Macaque Females Synchronize Sex not Cycles |
title_full | You Mate, I Mate: Macaque Females Synchronize Sex not Cycles |
title_fullStr | You Mate, I Mate: Macaque Females Synchronize Sex not Cycles |
title_full_unstemmed | You Mate, I Mate: Macaque Females Synchronize Sex not Cycles |
title_short | You Mate, I Mate: Macaque Females Synchronize Sex not Cycles |
title_sort | you mate, i mate: macaque females synchronize sex not cycles |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3192140/ https://www.ncbi.nlm.nih.gov/pubmed/22022541 http://dx.doi.org/10.1371/journal.pone.0026144 |
work_keys_str_mv | AT furtbauerines youmateimatemacaquefemalessynchronizesexnotcycles AT mundryroger youmateimatemacaquefemalessynchronizesexnotcycles AT heistermannmichael youmateimatemacaquefemalessynchronizesexnotcycles AT schulkeoliver youmateimatemacaquefemalessynchronizesexnotcycles AT ostnerjulia youmateimatemacaquefemalessynchronizesexnotcycles |