Literature DB >> 17451657

Top-down knowledge supports the retrieval of lexical information from degraded speech.

R Hannemann1, J Obleser, C Eulitz.   

Abstract

How is it that the human brain is capable of making sense from speech under many acoustically compromised conditions? The support through top-down knowledge is inevitable but can we identify brain measures of this matching process between degraded auditory input and possible meaning? To answer these questions, the present study investigated the modulation of the induced gamma-band activity (GBA) in the auditory domain in response to degraded speech. During an EEG experiment subjects first listened to digitally degraded unintelligible speech signals (derived from German nouns). In an exposure sequence, half of the nouns were presented in a non-degraded intelligible format and memorized, while in the crucial test sequence subjects listened to all degraded speech signals again and were asked to identify the words. The induced GBA (40-Hz range) showed an increase at left temporal electrode sites around 350 ms only for words correctly identified in the test sequence. No differences in induced GBA were evident in the baseline sequence; neither did the evoked brain potentials yield any comparable effect. We conclude that the observed enhancement in induced gamma-band activity reflects a matching process of top-down lexical memory traces with degraded sensory input to form a comprehendible speech percept. The findings are highly corroborant to analogous studies in the visual system. They lend further plausibility to a left-lateralized fronto-temporal network enabling lexically guided speech perception, and they demonstrate the complementary role of time-sensitive brain analyses in discerning the functional neuroanatomy of speech.

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Year:  2007        PMID: 17451657     DOI: 10.1016/j.brainres.2007.03.069

Source DB:  PubMed          Journal:  Brain Res        ISSN: 0006-8993            Impact factor:   3.252


  26 in total

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Authors:  Kirill V Nourski; Mitchell Steinschneider; Hiroyuki Oya; Hiroto Kawasaki; Matthew A Howard
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2.  Suppressed alpha oscillations predict intelligibility of speech and its acoustic details.

Authors:  Jonas Obleser; Nathan Weisz
Journal:  Cereb Cortex       Date:  2011-11-18       Impact factor: 5.357

3.  Word repetition priming-induced oscillations in auditory cortex: a magnetoencephalography study.

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Journal:  Neuroreport       Date:  2011-12-07       Impact factor: 1.837

4.  Acoustic landmarks drive delta-theta oscillations to enable speech comprehension by facilitating perceptual parsing.

Authors:  Keith B Doelling; Luc H Arnal; Oded Ghitza; David Poeppel
Journal:  Neuroimage       Date:  2013-06-19       Impact factor: 6.556

5.  Diffusion tensor imaging reveals white matter microstructure correlations with auditory processing ability.

Authors:  Vincent J Schmithorst; Scott K Holland; Elena Plante
Journal:  Ear Hear       Date:  2011 Mar-Apr       Impact factor: 3.570

6.  On the matching of top-down knowledge with sensory input in the perception of ambiguous speech.

Authors:  C Eulitz; R Hannemann
Journal:  BMC Neurosci       Date:  2010-06-02       Impact factor: 3.288

7.  When Broca goes uninformed: reduced information flow to Broca's area in schizophrenia patients with auditory hallucinations.

Authors:  Branislava Curcic-Blake; Edith Liemburg; Ans Vercammen; Marte Swart; Henderikus Knegtering; Richard Bruggeman; André Aleman
Journal:  Schizophr Bull       Date:  2012-10-15       Impact factor: 9.306

8.  Gamma phase locking modulated by phonological contrast during auditory comprehension in reading disability.

Authors:  Jooman Han; Maria Mody; Seppo P Ahlfors
Journal:  Neuroreport       Date:  2012-10-03       Impact factor: 1.837

9.  Brain oscillations during semantic evaluation of speech.

Authors:  Antoine J Shahin; Terence W Picton; Lee M Miller
Journal:  Brain Cogn       Date:  2009-03-25       Impact factor: 2.310

10.  Predictive top-down integration of prior knowledge during speech perception.

Authors:  Ediz Sohoglu; Jonathan E Peelle; Robert P Carlyon; Matthew H Davis
Journal:  J Neurosci       Date:  2012-06-20       Impact factor: 6.167

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