Literature DB >> 12805307

Frequency-specific interaural level difference tuning predicts spatial response patterns of space-specific neurons in the barn owl inferior colliculus.

Michael L Spezio1, Terry T Takahashi.   

Abstract

Space-specific neurons in the barn owl's inferior colliculus have spatial receptive fields (RFs) because of sensitivity to interaural time difference and frequency-specific interaural level difference (ILD). These neurons are assumed to be tuned to the frequency-specific ILDs occurring at their spatial RFs, but attempts to assess this tuning with traditional narrowband stimuli have had limited success. Indeed, tuning assessed in this manner, when processed via a linear model of spectral integration, typically explains only approximately half the variance in spatial response patterns. Here we report our findings that frequency-specific ILD tuning of space-specific neurons, when assessed from responses to broadband stimuli, predicted nearly 75% of the variance in spatial responses, using a linear model of spectral integration (p < 0.0001; n = 97 neurons). Furthermore, when we tested neurons using only those frequencies we found to be spatially relevant, we saw that their responses were similar to those elicited by broadband stimuli. When we used frequencies not identified as spatially relevant, such similarity was lacking. Furthermore, spectral components that elicited high firing rates when presented as narrowband stimuli were found in several cases to be irrelevant for or detrimental to the definition of spatial RFs. Thus, neurons achieved sharp spatial tuning by selecting for ILDs of a subset of spectral components in noise, some of which were not identified using narrowband stimuli.

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Mesh:

Year:  2003        PMID: 12805307      PMCID: PMC6740778     

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


  13 in total

1.  Specialization of binaural responses in ventral auditory cortices.

Authors:  Nathan C Higgins; Douglas A Storace; Monty A Escabí; Heather L Read
Journal:  J Neurosci       Date:  2010-10-27       Impact factor: 6.167

Review 2.  How the owl tracks its prey--II.

Authors:  Terry T Takahashi
Journal:  J Exp Biol       Date:  2010-10-15       Impact factor: 3.312

3.  Spike timing precision changes with spike rate adaptation in the owl's auditory space map.

Authors:  Clifford H Keller; Terry T Takahashi
Journal:  J Neurophysiol       Date:  2015-08-12       Impact factor: 2.714

4.  Sensitivity to interaural time difference and representation of azimuth in central nucleus of inferior colliculus in the barn owl.

Authors:  Peter Bremen; Iris Poganiatz; Mark von Campenhausen; Hermann Wagner
Journal:  J Comp Physiol A Neuroethol Sens Neural Behav Physiol       Date:  2006-09-26       Impact factor: 1.836

5.  Stimulus-specific adaptation to visual but not auditory motion direction in the barn owl's optic tectum.

Authors:  Dante F Wasmuht; Jose L Pena; Yoram Gutfreund
Journal:  Eur J Neurosci       Date:  2017-01-17       Impact factor: 3.386

Review 6.  Auditory processing, plasticity, and learning in the barn owl.

Authors:  Jose L Pena; William M DeBello
Journal:  ILAR J       Date:  2010

7.  Bilateral matching of frequency tuning in neural cross-correlators of the owl.

Authors:  Brian J Fischer; José Luis Peña
Journal:  Biol Cybern       Date:  2009-04-25       Impact factor: 2.086

8.  Cross-correlation in the auditory coincidence detectors of owls.

Authors:  Brian J Fischer; G Björn Christianson; José Luis Peña
Journal:  J Neurosci       Date:  2008-08-06       Impact factor: 6.167

Review 9.  New perspectives on the owl's map of auditory space.

Authors:  Jose L Pena; Yoram Gutfreund
Journal:  Curr Opin Neurobiol       Date:  2013-09-12       Impact factor: 6.627

10.  Multiplicative auditory spatial receptive fields created by a hierarchy of population codes.

Authors:  Brian J Fischer; Charles H Anderson; José Luis Peña
Journal:  PLoS One       Date:  2009-11-24       Impact factor: 3.240

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