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Temporal vocal features suggest different call-pattern generating mechanisms in mice and bats
BACKGROUND: Mice produce ultrasonic vocalizations in various inter-individual encounters and with high call rates. However, it is so far virtually unknown how these vocal patterns are generated. On the one hand, these vocal patterns could be embedded into the normal respiratory cycle, as happens in...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3846851/ https://www.ncbi.nlm.nih.gov/pubmed/24020588 http://dx.doi.org/10.1186/1471-2202-14-99 |
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author | Hage, Steffen R Gavrilov, Natalja Salomon, Ferdinand Stein, Anna M |
author_facet | Hage, Steffen R Gavrilov, Natalja Salomon, Ferdinand Stein, Anna M |
author_sort | Hage, Steffen R |
collection | PubMed |
description | BACKGROUND: Mice produce ultrasonic vocalizations in various inter-individual encounters and with high call rates. However, it is so far virtually unknown how these vocal patterns are generated. On the one hand, these vocal patterns could be embedded into the normal respiratory cycle, as happens in bats and other mammals that produce similar call rates and frequencies. On the other, mice could possess distinct vocal pattern generating systems that are capable of modulating the respiratory cycle, which is what happens in non-human and human primates. In the present study, we investigated the temporal call patterns of two different mammalian species, bats and mice, in order to differentiate between these two possibilities for mouse vocalizations. Our primary focus was on comparing the mechanisms for the production of rapid, successive ultrasound calls of comparable frequency ranges in the two species. RESULTS: We analyzed the temporal call pattern characteristics of mice, and we compared these characteristics to those of ultrasonic echolocation calls produced by horseshoe bats. We measured the distributions of call durations, call intervals, and inter-call intervals in the two species. In the bat, and consistent with previous studies, we found that call duration was independent of corresponding call intervals, and that it was negatively correlated with the corresponding inter-call interval. This indicates that echolocation call production mechanisms in the bat are highly correlated with the respiratory cycle. In contrast, call intervals in the mouse were directly correlated with call duration. Importantly, call duration was not, or was only slightly, correlated with inter-call intervals, consistent with the idea that vocal production in the mouse is largely independent of the respiratory cycle. CONCLUSIONS: Our findings suggest that ultrasonic vocalizations in mice are produced by call-pattern generating mechanisms that seem to be similar to those that have been found in primates. This is in contrast to the production mechanisms of ultrasonic echolocation calls in horseshoe bats. These results are particularly interesting, especially since mouse vocalizations have recently attracted increased attention as potential indicators for the degree of progression of several disease patterns in mouse models for neurodegenerative and neurodevelopmental disorders of humans. |
format | Online Article Text |
id | pubmed-3846851 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-38468512013-12-04 Temporal vocal features suggest different call-pattern generating mechanisms in mice and bats Hage, Steffen R Gavrilov, Natalja Salomon, Ferdinand Stein, Anna M BMC Neurosci Research Article BACKGROUND: Mice produce ultrasonic vocalizations in various inter-individual encounters and with high call rates. However, it is so far virtually unknown how these vocal patterns are generated. On the one hand, these vocal patterns could be embedded into the normal respiratory cycle, as happens in bats and other mammals that produce similar call rates and frequencies. On the other, mice could possess distinct vocal pattern generating systems that are capable of modulating the respiratory cycle, which is what happens in non-human and human primates. In the present study, we investigated the temporal call patterns of two different mammalian species, bats and mice, in order to differentiate between these two possibilities for mouse vocalizations. Our primary focus was on comparing the mechanisms for the production of rapid, successive ultrasound calls of comparable frequency ranges in the two species. RESULTS: We analyzed the temporal call pattern characteristics of mice, and we compared these characteristics to those of ultrasonic echolocation calls produced by horseshoe bats. We measured the distributions of call durations, call intervals, and inter-call intervals in the two species. In the bat, and consistent with previous studies, we found that call duration was independent of corresponding call intervals, and that it was negatively correlated with the corresponding inter-call interval. This indicates that echolocation call production mechanisms in the bat are highly correlated with the respiratory cycle. In contrast, call intervals in the mouse were directly correlated with call duration. Importantly, call duration was not, or was only slightly, correlated with inter-call intervals, consistent with the idea that vocal production in the mouse is largely independent of the respiratory cycle. CONCLUSIONS: Our findings suggest that ultrasonic vocalizations in mice are produced by call-pattern generating mechanisms that seem to be similar to those that have been found in primates. This is in contrast to the production mechanisms of ultrasonic echolocation calls in horseshoe bats. These results are particularly interesting, especially since mouse vocalizations have recently attracted increased attention as potential indicators for the degree of progression of several disease patterns in mouse models for neurodegenerative and neurodevelopmental disorders of humans. BioMed Central 2013-09-10 /pmc/articles/PMC3846851/ /pubmed/24020588 http://dx.doi.org/10.1186/1471-2202-14-99 Text en Copyright © 2013 Hage et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Hage, Steffen R Gavrilov, Natalja Salomon, Ferdinand Stein, Anna M Temporal vocal features suggest different call-pattern generating mechanisms in mice and bats |
title | Temporal vocal features suggest different call-pattern generating mechanisms in mice and bats |
title_full | Temporal vocal features suggest different call-pattern generating mechanisms in mice and bats |
title_fullStr | Temporal vocal features suggest different call-pattern generating mechanisms in mice and bats |
title_full_unstemmed | Temporal vocal features suggest different call-pattern generating mechanisms in mice and bats |
title_short | Temporal vocal features suggest different call-pattern generating mechanisms in mice and bats |
title_sort | temporal vocal features suggest different call-pattern generating mechanisms in mice and bats |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3846851/ https://www.ncbi.nlm.nih.gov/pubmed/24020588 http://dx.doi.org/10.1186/1471-2202-14-99 |
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