Literature DB >> 13679133

The origin of SFOAE microstructure in the guinea pig.

Shawn S Goodman1, Robert H Withnell, Christopher A Shera.   

Abstract

Human stimulus-frequency otoacoustic emissions (SFOAEs) evoked by low-level stimuli have previously been shown to have properties consistent with such emissions arising from a linear place-fixed reflection mechanism with SFOAE microstructure thought to be due to a variation in the effective reflectance with position along the cochlea [Zweig and Shera, J. Acoust. Soc. Am. 98 (1995) 2018-2047]. Here we report SFOAEs in the guinea pig obtained using a nonlinear extraction paradigm from the ear-canal recording that show amplitude and phase microstructure akin to that seen in human SFOAEs. Inverse Fourier analysis of the SFOAE spectrum indicates that SFOAEs in the guinea pig are a stimulus level-dependent mix of OAEs arising from linear-reflection and nonlinear-distortion mechanisms. Although the SFOAEs are dominated by OAE generated by a linear-reflection mechanism at low and moderate stimulus levels, nonlinear distortion can dominate some part of, or all of, the emission spectrum at high levels. Amplitude and phase microstructure in the guinea pig SFOAE is evidently a construct of (i). the complex addition of nonlinear-distortion and linear-reflection components; (ii). variation in the effective reflectance with position along the cochlea; and perhaps (iii). the complex addition of multiple intra-cochlear reflections.

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Year:  2003        PMID: 13679133     DOI: 10.1016/s0378-5955(03)00193-x

Source DB:  PubMed          Journal:  Hear Res        ISSN: 0378-5955            Impact factor:   3.208


  18 in total

1.  Reducing reflected contributions to ear-canal distortion product otoacoustic emissions in humans.

Authors:  Tiffany A Johnson; Stephen T Neely; Judy G Kopun; Michael P Gorga
Journal:  J Acoust Soc Am       Date:  2006-06       Impact factor: 1.840

2.  Use of stimulus-frequency otoacoustic emission latency and level to investigate cochlear mechanics in human ears.

Authors:  Kim S Schairer; John C Ellison; Denis Fitzpatrick; Douglas H Keefe
Journal:  J Acoust Soc Am       Date:  2006-08       Impact factor: 1.840

3.  Testing coherent reflection in chinchilla: Auditory-nerve responses predict stimulus-frequency emissions.

Authors:  Christopher A Shera; Arnold Tubis; Carrick L Talmadge
Journal:  J Acoust Soc Am       Date:  2008-07       Impact factor: 1.840

4.  Influence of stimulus parameters on amplitude-modulated stimulus frequency otoacoustic emissions.

Authors:  Tiffany A Johnson; Laura Beshaler
Journal:  J Acoust Soc Am       Date:  2013-08       Impact factor: 1.840

5.  Level dependence of distortion product otoacoustic emission phase is attributed to component mixing.

Authors:  Carolina Abdala; Sumitrajit Dhar; Radha Kalluri
Journal:  J Acoust Soc Am       Date:  2011-05       Impact factor: 1.840

6.  Simultaneous Intracochlear Pressure Measurements from Two Cochlear Locations: Propagation of Distortion Products in Gerbil.

Authors:  Wei Dong
Journal:  J Assoc Res Otolaryngol       Date:  2016-12-01

7.  Overshoot measured physiologically and psychophysically in the same human ears.

Authors:  Kyle P Walsh; Edward G Pasanen; Dennis McFadden
Journal:  Hear Res       Date:  2010-04-27       Impact factor: 3.208

8.  Electrically Evoked Medial Olivocochlear Efferent Effects on Stimulus Frequency Otoacoustic Emissions in Guinea Pigs.

Authors:  Maria A Berezina-Greene; John J Guinan
Journal:  J Assoc Res Otolaryngol       Date:  2016-10-31

9.  Stimulus Frequency Otoacoustic Emission Delays and Generating Mechanisms in Guinea Pigs, Chinchillas, and Simulations.

Authors:  Maria A Berezina-Greene; John J Guinan
Journal:  J Assoc Res Otolaryngol       Date:  2015-09-15

10.  Stimulus-frequency otoacoustic emission: measurements in humans and simulations with an active cochlear model.

Authors:  Yong-Sun Choi; Soo-Young Lee; Kourosh Parham; Stephen T Neely; Duck O Kim
Journal:  J Acoust Soc Am       Date:  2008-05       Impact factor: 1.840

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