A mechanism for antiphonal echolocation by free-tailed bats

Bats are highly social and spend much of their lives echolocating in the presence of other bats. To reduce the effects of acoustic interferences from other bats' echolocation calls, we hypothesized that bats might shift the timing of their pulse emissions to minimize temporal overlap with anoth...

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Published inAnimal behaviour Vol. 79; no. 4; pp. 787 - 796
Main Authors Jarvis, Jenna, Bohn, Kirsten M., Tressler, Jedediah, Smotherman, Michael
Format Journal Article
LanguageEnglish
Published Amsterdam Elsevier Ltd 01.04.2010
Elsevier
Harcourt Brace Jovanovich Ltd
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Abstract Bats are highly social and spend much of their lives echolocating in the presence of other bats. To reduce the effects of acoustic interferences from other bats' echolocation calls, we hypothesized that bats might shift the timing of their pulse emissions to minimize temporal overlap with another bat's echolocation pulses. To test this hypothesis, we investigated whether free-tailed bats, Tadarida brasiliensis, echolocating in the laboratory would shift the timing of their own pulse emissions in response to regularly repeating artificial acoustic stimuli. Each bat tested showed a robust phase-locked temporal pattern in pulse emissions that included an initial suppressive phase lasting more than 60 ms after stimulus onset, during which the probability of emitting pulses was reduced by more than 50%, followed by a compensatory rebound phase, the timing and amplitude of which were dependent on the temporal pattern of the stimulus. The responses were nonadapting and were largely insensitive to broad changes in the acoustic properties of the stimulus. Randomly occurring noise bursts also suppressed calling for up to 60 ms, but the time course of the compensatory rebound phase was more rapid than when the bats were responding to regularly repeating patterns of noise bursts. These findings provide the first quantitative description of how external stimuli may cause echolocating bats to alter the timing of subsequent pulse emissions.
AbstractList Bats are highly social and spend much of their lives echolocating in the presence of other bats. To reduce the effects of acoustic interferences from other bats' echolocation calls, we hypothesized that bats might shift the timing of their pulse emissions to minimize temporal overlap with another bat's echolocation pulses. To test this hypothesis, we investigated whether free-tailed bats, Tadarida brasiliensis, echolocating in the laboratory would shift the timing of their own pulse emissions in response to regularly repeating artificial acoustic stimuli. Each bat tested showed a robust phase-locked temporal pattern in pulse emissions that included an initial suppressive phase lasting more than 60ms after stimulus onset, during which the probability of emitting pulses was reduced by more than 50%, followed by a compensatory rebound phase, the timing and amplitude of which were dependent on the temporal pattern of the stimulus. The responses were nonadapting and were largely insensitive to broad changes in the acoustic properties of the stimulus. Randomly occurring noise bursts also suppressed calling for up to 60ms, but the time course of the compensatory rebound phase was more rapid than when the bats were responding to regularly repeating patterns of noise bursts. These findings provide the first quantitative description of how external stimuli may cause echolocating bats to alter the timing of subsequent pulse emissions.
Bats are highly social and spend much of their lives echolocating in the presence of other bats. To reduce the effects of acoustic interferences from other bats' echolocation calls, we hypothesized that bats might shift the timing of their pulse emissions to minimize temporal overlap with another bat's echolocation pulses. To test this hypothesis, we investigated whether free-tailed bats, Tadarida brasiliensis, echolocating in the laboratory would shift the timing of their own pulse emissions in response to regularly repeating artificial acoustic stimuli. Each bat tested showed a robust phase-locked temporal pattern in pulse emissions that included an initial suppressive phase lasting more than 60 ms after stimulus onset, during which the probability of emitting pulses was reduced by more than 50%, followed by a compensatory rebound phase, the timing and amplitude of which were dependent on the temporal pattern of the stimulus. The responses were nonadapting and were largely insensitive to broad changes in the acoustic properties of the stimulus. Randomly occurring noise bursts also suppressed calling for up to 60 ms, but the time course of the compensatory rebound phase was more rapid than when the bats were responding to regularly repeating patterns of noise bursts. These findings provide the first quantitative description of how external stimuli may cause echolocating bats to alter the timing of subsequent pulse emissions. [PUBLICATION ABSTRACT]
Bats are highly social and spend much of their lives echolocating in the presence of other bats. To reduce the effects of acoustic interferences from other bats' echolocation calls, we hypothesized that bats might shift the timing of their pulse emissions to minimize temporal overlap with another bat's echolocation pulses. To test this hypothesis we investigated whether free-tailed bats ( Tadarida brasiliensis ) echolocating in the lab would shift the timing of their own pulse emissions in response to regularly repeating artificial acoustic stimuli. A robust phase-locked temporal pattern in pulse emissions was displayed by every bat tested which included an initial suppressive phase lasting more than 60 ms after stimulus onset, during which the probability of emitting pulses was reduced by more than fifty percent, followed by a compensatory rebound phase, the timing and amplitude of which were dependent on the temporal pattern of the stimulus. The responses were non-adapting and were largely insensitive to broad changes in the acoustic properties of the stimulus. Randomly occurring noise-bursts also suppressed calling for up to 60 ms, but the time-course of the compensatory rebound phase was more rapid than when the bats were responding to regularly repeating patterns of noise bursts. These findings provide the first quantitative description of how external stimuli may cause echolocating bats to alter the timing of subsequent pulse emissions.
Bats are highly social and spend much of their lives echolocating in the presence of other bats. To reduce the effects of acoustic interferences from other bats' echolocation calls, we hypothesized that bats might shift the timing of their pulse emissions to minimize temporal overlap with another bat's echolocation pulses. To test this hypothesis we investigated whether free-tailed bats (Tadarida brasiliensis) echolocating in the lab would shift the timing of their own pulse emissions in response to regularly repeating artificial acoustic stimuli. A robust phase-locked temporal pattern in pulse emissions was displayed by every bat tested which included an initial suppressive phase lasting more than 60 ms after stimulus onset, during which the probability of emitting pulses was reduced by more than fifty percent, followed by a compensatory rebound phase, the timing and amplitude of which were dependent on the temporal pattern of the stimulus. The responses were non-adapting and were largely insensitive to broad changes in the acoustic properties of the stimulus. Randomly occurring noise-bursts also suppressed calling for up to 60 ms, but the time-course of the compensatory rebound phase was more rapid than when the bats were responding to regularly repeating patterns of noise bursts. These findings provide the first quantitative description of how external stimuli may cause echolocating bats to alter the timing of subsequent pulse emissions.
Bats are highly social and spend much of their lives echolocating in the presence of other bats. To reduce the effects of acoustic interferences from other bats' echolocation calls, we hypothesized that bats might shift the timing of their pulse emissions to minimize temporal overlap with another bat's echolocation pulses. To test this hypothesis, we investigated whether free-tailed bats, Tadarida brasiliensis, echolocating in the laboratory would shift the timing of their own pulse emissions in response to regularly repeating artificial acoustic stimuli. Each bat tested showed a robust phase-locked temporal pattern in pulse emissions that included an initial suppressive phase lasting more than 60 ms after stimulus onset, during which the probability of emitting pulses was reduced by more than 50%, followed by a compensatory rebound phase, the timing and amplitude of which were dependent on the temporal pattern of the stimulus. The responses were nonadapting and were largely insensitive to broad changes in the acoustic properties of the stimulus. Randomly occurring noise bursts also suppressed calling for up to 60 ms, but the time course of the compensatory rebound phase was more rapid than when the bats were responding to regularly repeating patterns of noise bursts. These findings provide the first quantitative description of how external stimuli may cause echolocating bats to alter the timing of subsequent pulse emissions.
Author Jarvis, Jenna
Bohn, Kirsten M.
Smotherman, Michael
Tressler, Jedediah
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Issue 4
Keywords acoustic masking
free-tailed bat
echolocation
bat
Tadarida brasiliensis
vocalization
noise
animal communication
Acoustic communication
Animal communication
Noise
Sound production
Acoustics
Vertebrata
Mammalia
Masking
Chiroptera
Echolocation
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Snippet Bats are highly social and spend much of their lives echolocating in the presence of other bats. To reduce the effects of acoustic interferences from other...
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SubjectTerms acoustic masking
Acoustics
Animal behavior
Animal cognition
Animal communication
Animal ethology
bat
Bats
Biological and medical sciences
echolocation
free-tailed bat
Fundamental and applied biological sciences. Psychology
Mammalia
Noise
Psychology. Psychoanalysis. Psychiatry
Tadarida brasiliensis
Vertebrates: general zoology, morphology, phylogeny, systematics, cytogenetics, geographical distribution
vocalization
Title A mechanism for antiphonal echolocation by free-tailed bats
URI https://dx.doi.org/10.1016/j.anbehav.2010.01.004
https://www.ncbi.nlm.nih.gov/pubmed/20419063
https://www.proquest.com/docview/224572259
https://search.proquest.com/docview/1835551677
https://search.proquest.com/docview/745927815
https://pubmed.ncbi.nlm.nih.gov/PMC2858338
Volume 79
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