Literature DB >> 25142131

Development of echolocation calls and neural selectivity for echolocation calls in the pallid bat.

Khaleel A Razak1, Zoltan M Fuzessery2.   

Abstract

Studies of birdsongs and neural selectivity for songs have provided important insights into principles of concurrent behavioral and auditory system development. Relatively little is known about mammalian auditory system development in terms of vocalizations or other behaviorally relevant sounds. This review suggests echolocating bats are suitable mammalian model systems to understand development of auditory behaviors. The simplicity of echolocation calls with known behavioral relevance and strong neural selectivity provides a platform to address how natural experience shapes cortical receptive field (RF) mechanisms. We summarize recent studies in the pallid bat that followed development of echolocation calls and cortical processing of such calls. We also discuss similar studies in the mustached bat for comparison. These studies suggest: (1) there are different developmental sensitive periods for different acoustic features of the same vocalization. The underlying basis is the capacity for some components of the RF to be modified independent of others. Some RF computations and maps involved in call processing are present even before the cochlea is mature and well before use of echolocation in flight. Others develop over a much longer time course. (2) Normal experience is required not just for refinement, but also for maintenance, of response properties that develop in an experience independent manner. (3) Experience utilizes millisecond range changes in timing of inhibitory and excitatory RF components as substrates to shape vocalization selectivity. We suggest that bat species and call diversity provide a unique opportunity to address developmental constraints in the evolution of neural mechanisms of vocalization processing.
© 2014 Wiley Periodicals, Inc.

Entities:  

Keywords:  auditory cortex; development; receptive fields; spectrotemporal processing; vocalizations

Mesh:

Year:  2014        PMID: 25142131      PMCID: PMC4336241          DOI: 10.1002/dneu.22226

Source DB:  PubMed          Journal:  Dev Neurobiol        ISSN: 1932-8451            Impact factor:   3.964


  79 in total

1.  Necessity for afferent activity to maintain eye-specific segregation in ferret lateral geniculate nucleus.

Authors:  B Chapman
Journal:  Science       Date:  2000-03-31       Impact factor: 47.728

Review 2.  From central pattern generator to sensory template in the evolution of birdsong.

Authors:  Masakazu Konishi
Journal:  Brain Lang       Date:  2010-10       Impact factor: 2.381

3.  Systematic representation of sound locations in the primary auditory cortex.

Authors:  Khaleel A Razak
Journal:  J Neurosci       Date:  2011-09-28       Impact factor: 6.167

4.  Development of spectral and temporal response selectivity in the auditory cortex.

Authors:  Edward F Chang; Shaowen Bao; Kazuo Imaizumi; Christoph E Schreiner; Michael M Merzenich
Journal:  Proc Natl Acad Sci U S A       Date:  2005-11-01       Impact factor: 11.205

5.  Combination-sensitive neurons in the medial geniculate body of the mustached bat: encoding of target range information.

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

6.  Syllable acoustics, temporal patterns, and call composition vary with behavioral context in Mexican free-tailed bats.

Authors:  Kirsten M Bohn; Barbara Schmidt-French; Sean T Ma; George D Pollak
Journal:  J Acoust Soc Am       Date:  2008-09       Impact factor: 1.840

7.  GABA shapes selectivity for the rate and direction of frequency-modulated sweeps in the auditory cortex.

Authors:  Khaleel A Razak; Zoltan M Fuzessery
Journal:  J Neurophysiol       Date:  2009-06-24       Impact factor: 2.714

8.  Biosonar and neural computation in bats.

Authors:  N Suga
Journal:  Sci Am       Date:  1990-06       Impact factor: 2.142

Review 9.  Neural maps for target range in the auditory cortex of echolocating bats.

Authors:  M Kössl; J C Hechavarria; C Voss; S Macias; E C Mora; M Vater
Journal:  Curr Opin Neurobiol       Date:  2013-09-17       Impact factor: 6.627

10.  Response selectivity for multiple dimensions of frequency sweeps in the pallid bat inferior colliculus.

Authors:  Z M Fuzessery
Journal:  J Neurophysiol       Date:  1994-09       Impact factor: 2.714

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  1 in total

1.  Hearing, echolocation, and beam steering from day 0 in tongue-clicking bats.

Authors:  Grace C Smarsh; Yifat Tarnovsky; Yossi Yovel
Journal:  Proc Biol Sci       Date:  2021-10-27       Impact factor: 5.349

  1 in total

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