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Social foraging in vampire bats is predicted by long-term cooperative relationships
Stable social bonds in group-living animals can provide greater access to food. A striking example is that female vampire bats often regurgitate blood to socially bonded kin and nonkin that failed in their nightly hunt. Food-sharing relationships form via preferred associations and social grooming w...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8460024/ https://www.ncbi.nlm.nih.gov/pubmed/34555014 http://dx.doi.org/10.1371/journal.pbio.3001366 |
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author | Ripperger, Simon P. Carter, Gerald G. |
author_facet | Ripperger, Simon P. Carter, Gerald G. |
author_sort | Ripperger, Simon P. |
collection | PubMed |
description | Stable social bonds in group-living animals can provide greater access to food. A striking example is that female vampire bats often regurgitate blood to socially bonded kin and nonkin that failed in their nightly hunt. Food-sharing relationships form via preferred associations and social grooming within roosts. However, it remains unclear whether these cooperative relationships extend beyond the roost. To evaluate if long-term cooperative relationships in vampire bats play a role in foraging, we tested if foraging encounters measured by proximity sensors could be explained by wild roosting proximity, kinship, or rates of co-feeding, social grooming, and food sharing during 21 months in captivity. We assessed evidence for 6 hypothetical scenarios of social foraging, ranging from individual to collective hunting. We found that closely bonded female vampire bats departed their roost separately, but often reunited far outside the roost. Repeating foraging encounters were predicted by within-roost association and histories of cooperation in captivity, even when accounting for kinship. Foraging bats demonstrated both affiliative and competitive interactions with different social calls linked to each interaction type. We suggest that social foraging could have implications for social evolution if “local” within-roost cooperation and “global” outside-roost competition enhances fitness interdependence between frequent roostmates. |
format | Online Article Text |
id | pubmed-8460024 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-84600242021-09-24 Social foraging in vampire bats is predicted by long-term cooperative relationships Ripperger, Simon P. Carter, Gerald G. PLoS Biol Short Reports Stable social bonds in group-living animals can provide greater access to food. A striking example is that female vampire bats often regurgitate blood to socially bonded kin and nonkin that failed in their nightly hunt. Food-sharing relationships form via preferred associations and social grooming within roosts. However, it remains unclear whether these cooperative relationships extend beyond the roost. To evaluate if long-term cooperative relationships in vampire bats play a role in foraging, we tested if foraging encounters measured by proximity sensors could be explained by wild roosting proximity, kinship, or rates of co-feeding, social grooming, and food sharing during 21 months in captivity. We assessed evidence for 6 hypothetical scenarios of social foraging, ranging from individual to collective hunting. We found that closely bonded female vampire bats departed their roost separately, but often reunited far outside the roost. Repeating foraging encounters were predicted by within-roost association and histories of cooperation in captivity, even when accounting for kinship. Foraging bats demonstrated both affiliative and competitive interactions with different social calls linked to each interaction type. We suggest that social foraging could have implications for social evolution if “local” within-roost cooperation and “global” outside-roost competition enhances fitness interdependence between frequent roostmates. Public Library of Science 2021-09-23 /pmc/articles/PMC8460024/ /pubmed/34555014 http://dx.doi.org/10.1371/journal.pbio.3001366 Text en https://creativecommons.org/publicdomain/zero/1.0/This is an open access article, free of all copyright, and may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. The work is made available under the Creative Commons CC0 (https://creativecommons.org/publicdomain/zero/1.0/) public domain dedication. |
spellingShingle | Short Reports Ripperger, Simon P. Carter, Gerald G. Social foraging in vampire bats is predicted by long-term cooperative relationships |
title | Social foraging in vampire bats is predicted by long-term cooperative relationships |
title_full | Social foraging in vampire bats is predicted by long-term cooperative relationships |
title_fullStr | Social foraging in vampire bats is predicted by long-term cooperative relationships |
title_full_unstemmed | Social foraging in vampire bats is predicted by long-term cooperative relationships |
title_short | Social foraging in vampire bats is predicted by long-term cooperative relationships |
title_sort | social foraging in vampire bats is predicted by long-term cooperative relationships |
topic | Short Reports |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8460024/ https://www.ncbi.nlm.nih.gov/pubmed/34555014 http://dx.doi.org/10.1371/journal.pbio.3001366 |
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