Literature DB >> 16266165

Delays of stimulus-frequency otoacoustic emissions and cochlear vibrations contradict the theory of coherent reflection filtering.

Jonathan H Siegel1, Amanda J Cerka, Alberto Recio-Spinoso, Andrei N Temchin, Pim van Dijk, Mario A Ruggero.   

Abstract

When stimulated by tones, the ear appears to emit tones of its own, stimulus-frequency otoacoustic emissions (SFOAEs). SFOAEs were measured in 17 chinchillas and their group delays were compared with a place map of basilar-membrane vibration group delays measured at the characteristic frequency. The map is based on Wiener-kernel analysis of responses to noise of auditory-nerve fibers corroborated by measurements of vibrations at several basilar-membrane sites. SFOAE group delays were similar to, or shorter than, basilar-membrane group delays for frequencies >4 kHz and <4 kHz, respectively. Such short delays contradict the generally accepted "theory of coherent reflection filtering" [Zweig and Shera, J. Acoust. Soc. Am. 98, 2018-2047 (1995)], which predicts that the group delays of SFOAEs evoked by low-level tones approximately equal twice the basilar-membrane group delays. The results for frequencies higher than 4 kHz are compatible with hypotheses of SFOAE propagation to the stapes via acoustic waves or fluid coupling, or via reverse basilar membrane traveling waves with speeds corresponding to the signal-front delays, rather than the group delays, of the forward waves. The results for frequencies lower than 4 kHz cannot be explained by hypotheses based on waves propagating to and from their characteristic places in the cochlea.

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Year:  2005        PMID: 16266165     DOI: 10.1121/1.2005867

Source DB:  PubMed          Journal:  J Acoust Soc Am        ISSN: 0001-4966            Impact factor:   1.840


  69 in total

1.  Perception of across-frequency asynchrony and the role of cochlear delays.

Authors:  Magdalena Wojtczak; Jordan A Beim; Christophe Micheyl; Andrew J Oxenham
Journal:  J Acoust Soc Am       Date:  2012-01       Impact factor: 1.840

2.  Effects of low-frequency biasing on otoacoustic and neural measures suggest that stimulus-frequency otoacoustic emissions originate near the peak region of the traveling wave.

Authors:  Jeffery T Lichtenhan
Journal:  J Assoc Res Otolaryngol       Date:  2011-10-15

3.  Direction of wave propagation in the cochlea for internally excited basilar membrane.

Authors:  Yizeng Li; Karl Grosh
Journal:  J Acoust Soc Am       Date:  2012-06       Impact factor: 1.840

4.  Coherent reflection without traveling waves: on the origin of long-latency otoacoustic emissions in lizards.

Authors:  Christopher Bergevin; Christopher A Shera
Journal:  J Acoust Soc Am       Date:  2010-04       Impact factor: 1.840

5.  Fast reverse propagation of sound in the living cochlea.

Authors:  Wenxuan He; Anders Fridberger; Edward Porsov; Tianying Ren
Journal:  Biophys J       Date:  2010-06-02       Impact factor: 4.033

6.  Distortion product otoacoustic emissions measured as vibration on the eardrum of human subjects.

Authors:  E Dalhoff; D Turcanu; H-P Zenner; A W Gummer
Journal:  Proc Natl Acad Sci U S A       Date:  2007-01-22       Impact factor: 11.205

7.  Two-tone distortion at different longitudinal locations on the basilar membrane.

Authors:  Wenxuan He; Alfred L Nuttall; Tianying Ren
Journal:  Hear Res       Date:  2007-02-12       Impact factor: 3.208

8.  Neural representation of spectral and temporal information in speech.

Authors:  Eric D Young
Journal:  Philos Trans R Soc Lond B Biol Sci       Date:  2008-03-12       Impact factor: 6.237

9.  Inverted direction of wave propagation (IDWP) in the cochlea.

Authors:  Egbert de Boer; Jiefu Zheng; Edward Porsov; Alfred L Nuttall
Journal:  J Acoust Soc Am       Date:  2008-03       Impact factor: 1.840

10.  Reverse wave propagation in the cochlea.

Authors:  Wenxuan He; Anders Fridberger; Edward Porsov; Karl Grosh; Tianying Ren
Journal:  Proc Natl Acad Sci U S A       Date:  2008-02-12       Impact factor: 11.205

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