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Ultrashort-range, high-frequency communication by female mice shapes social interactions

Animals engage in complex social encounters that influence social groups and resource allocation. During these encounters, acoustic signals, used at both short and long ranges, play pivotal roles in regulating the behavior of conspecifics. Mice, for instance, emit ultrasonic vocalizations, signals a...

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Autores principales: Warren, M. R., Clein, R. S., Spurrier, M. S., Roth, E. D., Neunuebel, J. P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7021676/
https://www.ncbi.nlm.nih.gov/pubmed/32060312
http://dx.doi.org/10.1038/s41598-020-59418-0
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author Warren, M. R.
Clein, R. S.
Spurrier, M. S.
Roth, E. D.
Neunuebel, J. P.
author_facet Warren, M. R.
Clein, R. S.
Spurrier, M. S.
Roth, E. D.
Neunuebel, J. P.
author_sort Warren, M. R.
collection PubMed
description Animals engage in complex social encounters that influence social groups and resource allocation. During these encounters, acoustic signals, used at both short and long ranges, play pivotal roles in regulating the behavior of conspecifics. Mice, for instance, emit ultrasonic vocalizations, signals above the range of human hearing, during close-range social interactions. How these signals shape behavior, however, is unknown due to the difficulty in discerning which mouse in a group is vocalizing. To overcome this impediment, we used an eight-channel microphone array system to determine which mouse emitted individual vocal signals during 30 minutes of unrestrained social interaction between a female and a single male or female conspecific. Females modulated both the timing and context of vocal emission based upon their social partner. Compared to opposite-sex pairings, females in same-sex pairs vocalized when closer to a social partner and later in the 30 minutes of social engagement. Remarkably, we found that female mice exhibited no immediate changes in acceleration (movement) to male-emitted vocal signals. Both males and females, in contrast, modulated their behavior following female-emitted vocal signals in a context-dependent manner. Thus, our results suggest female vocal signals function as a means of ultrashort-range communication that shapes mouse social behavior.
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spelling pubmed-70216762020-02-24 Ultrashort-range, high-frequency communication by female mice shapes social interactions Warren, M. R. Clein, R. S. Spurrier, M. S. Roth, E. D. Neunuebel, J. P. Sci Rep Article Animals engage in complex social encounters that influence social groups and resource allocation. During these encounters, acoustic signals, used at both short and long ranges, play pivotal roles in regulating the behavior of conspecifics. Mice, for instance, emit ultrasonic vocalizations, signals above the range of human hearing, during close-range social interactions. How these signals shape behavior, however, is unknown due to the difficulty in discerning which mouse in a group is vocalizing. To overcome this impediment, we used an eight-channel microphone array system to determine which mouse emitted individual vocal signals during 30 minutes of unrestrained social interaction between a female and a single male or female conspecific. Females modulated both the timing and context of vocal emission based upon their social partner. Compared to opposite-sex pairings, females in same-sex pairs vocalized when closer to a social partner and later in the 30 minutes of social engagement. Remarkably, we found that female mice exhibited no immediate changes in acceleration (movement) to male-emitted vocal signals. Both males and females, in contrast, modulated their behavior following female-emitted vocal signals in a context-dependent manner. Thus, our results suggest female vocal signals function as a means of ultrashort-range communication that shapes mouse social behavior. Nature Publishing Group UK 2020-02-14 /pmc/articles/PMC7021676/ /pubmed/32060312 http://dx.doi.org/10.1038/s41598-020-59418-0 Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Warren, M. R.
Clein, R. S.
Spurrier, M. S.
Roth, E. D.
Neunuebel, J. P.
Ultrashort-range, high-frequency communication by female mice shapes social interactions
title Ultrashort-range, high-frequency communication by female mice shapes social interactions
title_full Ultrashort-range, high-frequency communication by female mice shapes social interactions
title_fullStr Ultrashort-range, high-frequency communication by female mice shapes social interactions
title_full_unstemmed Ultrashort-range, high-frequency communication by female mice shapes social interactions
title_short Ultrashort-range, high-frequency communication by female mice shapes social interactions
title_sort ultrashort-range, high-frequency communication by female mice shapes social interactions
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7021676/
https://www.ncbi.nlm.nih.gov/pubmed/32060312
http://dx.doi.org/10.1038/s41598-020-59418-0
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