2004
DOI: 10.1139/z04-074
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Conspecifics influence call design in the Brazilian free-tailed bat,Tadarida brasiliensis

Abstract: The Brazilian free-tailed bat, Tadarida brasiliensis (Saint-Hilaire, 1824), uses calls that represent a broad continuum of design variation which is dependent upon habitat and situation, and exhibits characteristic changes in call design as bats close in on airborne targets. Here we demonstrate the influence of conspecifics on call design. We found that the peak frequency used in calls varies more as the number of bats flying in the same space increases (measured from single bats and pairs of bats). We investi… Show more

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Cited by 69 publications
(66 citation statements)
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“…Theoretically, changing bandwidth is one method that a sonar receiver could use to circumvent jamming (Simmons and Stein, 1980). Recently, Tadarida brasiliensis has been shown to shift its search call frequencies upward when dynamically challenged with the playback of a conspecific echolocation sequence (Gillam et al, 2007) experimentally corroborating previous correlational field studies (Orbist, 1995;Surlykke and Moss, 2000;Ratcliffe et al, 2004;Ulanovsky et al, 2004). The tiger moths used in these experiments and an assemblage of tropical tiger moths (Barber and Conner, 2006) respond during the end of the approach phase of the echolocation attack, when the spectral bandwidth of the biosonar cries has reached a near maximum (Simmons et al, 1978;Schnitzler and Kalko, 2001).…”
Section: Bioacousticssupporting
confidence: 72%
“…Theoretically, changing bandwidth is one method that a sonar receiver could use to circumvent jamming (Simmons and Stein, 1980). Recently, Tadarida brasiliensis has been shown to shift its search call frequencies upward when dynamically challenged with the playback of a conspecific echolocation sequence (Gillam et al, 2007) experimentally corroborating previous correlational field studies (Orbist, 1995;Surlykke and Moss, 2000;Ratcliffe et al, 2004;Ulanovsky et al, 2004). The tiger moths used in these experiments and an assemblage of tropical tiger moths (Barber and Conner, 2006) respond during the end of the approach phase of the echolocation attack, when the spectral bandwidth of the biosonar cries has reached a near maximum (Simmons et al, 1978;Schnitzler and Kalko, 2001).…”
Section: Bioacousticssupporting
confidence: 72%
“…The lengthening of call durations that we observed may be an attempt to do the same. Bats also shift call frequency in order to avoid jamming by conspecifics Ratcliffe et al, 2004;Ulanovsky et al, 2004), chorusing insects and synthetic narrowband noise (Bates et al, 2008;Tressler and Smotherman, 2009), but not broadband noise (Bates et al, 2008;Tressler and Smotherman, 2009). We did not observe bats changing the frequency of their emissions in response to moth clicks, only the durations and pulse intervals.…”
Section: Bat Echolocation and Flight Responses To Moth Clicks Supportmentioning
confidence: 99%
“…Call design separation was affected by the spatial distance between paired bats and baseline similarity in call design, which further suggests that the bat actively adjusts its call design to avoid signal interference from conspecifics. Several bat species, including R. hardwickei, Balantiopteryx plicata, T. brasiliensis and Tadarida teniotis, have been reported to adjust their call frequencies when flying in groups (Bartonicka et al, 2007;Habersetzer, 1981;Ibánez et al, 2004;Ratcliffe et al, 2004;Ulanovsky et al, 2004). Some bat species modified temporal features rather than spectral features of their vocalizations to avoid call interference from conspecifics (Obrist, 1995).…”
Section: Global Signal Adjustments In the Presence Of Conspecificsmentioning
confidence: 99%