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Different Auditory Feedback Control for Echolocation and Communication in Horseshoe Bats

Auditory feedback from the animal's own voice is essential during bat echolocation: to optimize signal detection, bats continuously adjust various call parameters in response to changing echo signals. Auditory feedback seems also necessary for controlling many bat communication calls, although...

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Autores principales: Liu, Ying, Feng, Jiang, Metzner, Walter
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3634746/
https://www.ncbi.nlm.nih.gov/pubmed/23638137
http://dx.doi.org/10.1371/journal.pone.0062710
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author Liu, Ying
Feng, Jiang
Metzner, Walter
author_facet Liu, Ying
Feng, Jiang
Metzner, Walter
author_sort Liu, Ying
collection PubMed
description Auditory feedback from the animal's own voice is essential during bat echolocation: to optimize signal detection, bats continuously adjust various call parameters in response to changing echo signals. Auditory feedback seems also necessary for controlling many bat communication calls, although it remains unclear how auditory feedback control differs in echolocation and communication. We tackled this question by analyzing echolocation and communication in greater horseshoe bats, whose echolocation pulses are dominated by a constant frequency component that matches the frequency range they hear best. To maintain echoes within this “auditory fovea”, horseshoe bats constantly adjust their echolocation call frequency depending on the frequency of the returning echo signal. This Doppler-shift compensation (DSC) behavior represents one of the most precise forms of sensory-motor feedback known. We examined the variability of echolocation pulses emitted at rest (resting frequencies, RFs) and one type of communication signal which resembles an echolocation pulse but is much shorter (short constant frequency communication calls, SCFs) and produced only during social interactions. We found that while RFs varied from day to day, corroborating earlier studies in other constant frequency bats, SCF-frequencies remained unchanged. In addition, RFs overlapped for some bats whereas SCF-frequencies were always distinctly different. This indicates that auditory feedback during echolocation changed with varying RFs but remained constant or may have been absent during emission of SCF calls for communication. This fundamentally different feedback mechanism for echolocation and communication may have enabled these bats to use SCF calls for individual recognition whereas they adjusted RF calls to accommodate the daily shifts of their auditory fovea.
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spelling pubmed-36347462013-05-01 Different Auditory Feedback Control for Echolocation and Communication in Horseshoe Bats Liu, Ying Feng, Jiang Metzner, Walter PLoS One Research Article Auditory feedback from the animal's own voice is essential during bat echolocation: to optimize signal detection, bats continuously adjust various call parameters in response to changing echo signals. Auditory feedback seems also necessary for controlling many bat communication calls, although it remains unclear how auditory feedback control differs in echolocation and communication. We tackled this question by analyzing echolocation and communication in greater horseshoe bats, whose echolocation pulses are dominated by a constant frequency component that matches the frequency range they hear best. To maintain echoes within this “auditory fovea”, horseshoe bats constantly adjust their echolocation call frequency depending on the frequency of the returning echo signal. This Doppler-shift compensation (DSC) behavior represents one of the most precise forms of sensory-motor feedback known. We examined the variability of echolocation pulses emitted at rest (resting frequencies, RFs) and one type of communication signal which resembles an echolocation pulse but is much shorter (short constant frequency communication calls, SCFs) and produced only during social interactions. We found that while RFs varied from day to day, corroborating earlier studies in other constant frequency bats, SCF-frequencies remained unchanged. In addition, RFs overlapped for some bats whereas SCF-frequencies were always distinctly different. This indicates that auditory feedback during echolocation changed with varying RFs but remained constant or may have been absent during emission of SCF calls for communication. This fundamentally different feedback mechanism for echolocation and communication may have enabled these bats to use SCF calls for individual recognition whereas they adjusted RF calls to accommodate the daily shifts of their auditory fovea. Public Library of Science 2013-04-24 /pmc/articles/PMC3634746/ /pubmed/23638137 http://dx.doi.org/10.1371/journal.pone.0062710 Text en © 2013 Liu 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
Liu, Ying
Feng, Jiang
Metzner, Walter
Different Auditory Feedback Control for Echolocation and Communication in Horseshoe Bats
title Different Auditory Feedback Control for Echolocation and Communication in Horseshoe Bats
title_full Different Auditory Feedback Control for Echolocation and Communication in Horseshoe Bats
title_fullStr Different Auditory Feedback Control for Echolocation and Communication in Horseshoe Bats
title_full_unstemmed Different Auditory Feedback Control for Echolocation and Communication in Horseshoe Bats
title_short Different Auditory Feedback Control for Echolocation and Communication in Horseshoe Bats
title_sort different auditory feedback control for echolocation and communication in horseshoe bats
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3634746/
https://www.ncbi.nlm.nih.gov/pubmed/23638137
http://dx.doi.org/10.1371/journal.pone.0062710
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