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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...

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Autores principales: Fürtbauer, Ines, Mundry, Roger, Heistermann, Michael, Schülke, Oliver, Ostner, Julia
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
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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.
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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
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