Literature DB >> 9030631

Spatially selective auditory responses in the superior colliculus of the echolocating bat.

D E Valentine1, C F Moss.   

Abstract

When a bat approaches a target, it continuously modifies its echolocation sounds and relies on incoming echo information to shape the characteristics of its subsequent sonar cries. In addition, acoustic information about the azimuth and elevation of a sonar target elicits orienting movements of the head and pinnae toward the sound source. This requires a common sensorimotor interface, where echo information is used to guide motor behaviors. Using single-unit neurophysiological methods and free-field auditory stimulation, we present data on biologically relevant specializations in the superior colliculus (SC) of the bat for orientation by sonar. In the bat's SC, two classes of spatially tuned neurons are distinguished by their sensitivity to echoes. One population shows facilitated, delay-tuned responses to pairs of sounds, simulating sonar emissions and echoes. Delay tuning, related to encoding target range, may play a role in guiding motor responses in echolocation, because the bat adjusts its emissions with changes in target distance. The delay-facilitated response depends on the direction of stimulation and on the temporal relationship between the simulated emission and echo in the sound pair, suggesting that this class of neurons represents the location of a target in three dimensions. A second population encodes the target in two dimensions, azimuth and elevation, and does not show a facilitated response to echoes delivered from any locus. Encoding of azimuth and elevation may be important for directing head aim, and this class may function in transforming auditory spatial information into signals used to guide acoustic orientation.

Mesh:

Year:  1997        PMID: 9030631      PMCID: PMC6573370     

Source DB:  PubMed          Journal:  J Neurosci        ISSN: 0270-6474            Impact factor:   6.167


  37 in total

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Authors:  J F Olsen; N Suga
Journal:  J Neurophysiol       Date:  1991-06       Impact factor: 2.714

2.  Corticofugal modulation of time-domain processing of biosonar information in bats.

Authors:  J Yan; N Suga
Journal:  Science       Date:  1996-08-23       Impact factor: 47.728

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Authors:  M Kawasaki; D Margoliash; N Suga
Journal:  J Neurophysiol       Date:  1988-02       Impact factor: 2.714

4.  Between the retinotectal projection and directed movement: topography of a sensorimotor interface.

Authors:  P Grobstein
Journal:  Brain Behav Evol       Date:  1988       Impact factor: 1.808

5.  Neural control of vocalization in bats: mapping of brainstem areas with electrical microstimulation eliciting species-specific echolocation calls in the rufous horseshoe bat.

Authors:  G Schuller; S Radtke-Schuller
Journal:  Exp Brain Res       Date:  1990       Impact factor: 1.972

6.  The resolution of target range by echolocating bats.

Authors:  J A Simmons
Journal:  J Acoust Soc Am       Date:  1973-07       Impact factor: 1.840

7.  Response properties of single units in the dorsal nucleus of the lateral lemniscus and paralemniscal zone of an echolocating bat.

Authors:  E Covey
Journal:  J Neurophysiol       Date:  1993-03       Impact factor: 2.714

8.  Neural axis representing target range in the auditory cortex of the mustache bat.

Authors:  N Suga; W E O'Neill
Journal:  Science       Date:  1979-10-19       Impact factor: 47.728

9.  Auditory and visual maps of space in the optic tectum of the owl.

Authors:  E I Knudsen
Journal:  J Neurosci       Date:  1982-09       Impact factor: 6.167

10.  Spatial tuning of auditory neurons in the superior colliculus of the echolocating bat, Myotis lucifugus.

Authors:  D Wong
Journal:  Hear Res       Date:  1984-12       Impact factor: 3.208

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  19 in total

1.  The corticofugal system for hearing: recent progress.

Authors:  N Suga; E Gao; Y Zhang; X Ma; J F Olsen
Journal:  Proc Natl Acad Sci U S A       Date:  2000-10-24       Impact factor: 11.205

2.  Vocal premotor activity in the superior colliculus.

Authors:  Shiva R Sinha; Cynthia F Moss
Journal:  J Neurosci       Date:  2007-01-03       Impact factor: 6.167

3.  What the bat's voice tells the bat's brain.

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Journal:  Proc Natl Acad Sci U S A       Date:  2008-06-18       Impact factor: 11.205

4.  Echo-acoustic flow shapes object representation in spatially complex acoustic scenes.

Authors:  Wolfgang Greiter; Uwe Firzlaff
Journal:  J Neurophysiol       Date:  2017-03-08       Impact factor: 2.714

5.  Functional Organization and Dynamic Activity in the Superior Colliculus of the Echolocating Bat, Eptesicus fuscus.

Authors:  Melville J Wohlgemuth; Ninad B Kothari; Cynthia F Moss
Journal:  J Neurosci       Date:  2017-11-27       Impact factor: 6.167

6.  Near-field discrimination of sound source distance in the rabbit.

Authors:  Shigeyuki Kuwada; Duck O Kim; Kelly-Jo Koch; Kristina S Abrams; Fabio Idrobo; Pavel Zahorik; Laurel H Carney
Journal:  J Assoc Res Otolaryngol       Date:  2015-01-17

7.  Visually guided gradation of prey capture movements in larval zebrafish.

Authors:  Bradley W Patterson; Aliza O Abraham; Malcolm A MacIver; David L McLean
Journal:  J Exp Biol       Date:  2013-04-25       Impact factor: 3.312

8.  Midbrain auditory selectivity to natural sounds.

Authors:  Melville J Wohlgemuth; Cynthia F Moss
Journal:  Proc Natl Acad Sci U S A       Date:  2016-02-16       Impact factor: 11.205

9.  Flying in silence: Echolocating bats cease vocalizing to avoid sonar jamming.

Authors:  Chen Chiu; Wei Xian; Cynthia F Moss
Journal:  Proc Natl Acad Sci U S A       Date:  2008-08-25       Impact factor: 11.205

10.  Dynamic representation of 3D auditory space in the midbrain of the free-flying echolocating bat.

Authors:  Ninad B Kothari; Melville J Wohlgemuth; Cynthia F Moss
Journal:  Elife       Date:  2018-04-10       Impact factor: 8.140

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