JN Fuel your research with LabChart
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


J Neurophysiol 86: 2761-2788, 2001;
0022-3077/01 $5.00
This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in ISI Web of Science
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via ISI Web of Science (25)
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Fishman, Y. I.
Right arrow Articles by Steinschneider, M.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Fishman, Y. I.
Right arrow Articles by Steinschneider, M.

The Journal of Neurophysiology Vol. 86 No. 6 December 2001, pp. 2761-2788
Copyright ©2001 by the American Physiological Society

Consonance and Dissonance of Musical Chords: Neural Correlates in Auditory Cortex of Monkeys and Humans

Yonatan I. Fishman,1 Igor O. Volkov,2 M. Daniel Noh,2 P. Charles Garell,2 Hans Bakken,2 Joseph C. Arezzo,1 Matthew A. Howard,2 and Mitchell Steinschneider1

 1Department of Neuroscience, Albert Einstein College of Medicine, Bronx, New York 10461; and  2Department of Surgery, Division of Neurosurgery, University of Iowa College of Medicine, Iowa City, Iowa 52242

Fishman, Yonatan I., Igor O. Volkov, M. Daniel Noh, P. Charles Garell, Hans Bakken, Joseph C. Arezzo, Matthew A. Howard, and Mitchell Steinschneider. Consonance and Dissonance of Musical Chords: Neural Correlates in Auditory Cortex of Monkeys and Humans. J. Neurophysiol. 86: 2761-2788, 2001. Some musical chords sound pleasant, or consonant, while others sound unpleasant, or dissonant. Helmholtz's psychoacoustic theory of consonance and dissonance attributes the perception of dissonance to the sensation of "beats" and "roughness" caused by interactions in the auditory periphery between adjacent partials of complex tones comprising a musical chord. Conversely, consonance is characterized by the relative absence of beats and roughness. Physiological studies in monkeys suggest that roughness may be represented in primary auditory cortex (A1) by oscillatory neuronal ensemble responses phase-locked to the amplitude-modulated temporal envelope of complex sounds. However, it remains unknown whether phase-locked responses also underlie the representation of dissonance in auditory cortex. In the present study, responses evoked by musical chords with varying degrees of consonance and dissonance were recorded in A1 of awake macaques and evaluated using auditory-evoked potential (AEP), multiunit activity (MUA), and current-source density (CSD) techniques. In parallel studies, intracranial AEPs evoked by the same musical chords were recorded directly from the auditory cortex of two human subjects undergoing surgical evaluation for medically intractable epilepsy. Chords were composed of two simultaneous harmonic complex tones. The magnitude of oscillatory phase-locked activity in A1 of the monkey correlates with the perceived dissonance of the musical chords. Responses evoked by dissonant chords, such as minor and major seconds, display oscillations phase-locked to the predicted difference frequencies, whereas responses evoked by consonant chords, such as octaves and perfect fifths, display little or no phase-locked activity. AEPs recorded in Heschl's gyrus display strikingly similar oscillatory patterns to those observed in monkey A1, with dissonant chords eliciting greater phase-locked activity than consonant chords. In contrast to recordings in Heschl's gyrus, AEPs recorded in the planum temporale do not display significant phase-locked activity, suggesting functional differentiation of auditory cortical regions in humans. These findings support the relevance of synchronous phase-locked neural ensemble activity in A1 for the physiological representation of sensory dissonance in humans and highlight the merits of complementary monkey/human studies in the investigation of neural substrates underlying auditory perception.




This article has been cited by other articles:


Home page
BrainHome page
N. Gosselin, S. Samson, R. Adolphs, M. Noulhiane, M. Roy, D. Hasboun, M. Baulac, and I. Peretz
Emotional responses to unpleasant music correlates with damage to the parahippocampal cortex
Brain, October 1, 2006; 129(10): 2585 - 2592.
[Abstract] [Full Text] [PDF]


Home page
Ann. N. Y. Acad. Sci.Home page
J. McDERMOTT and M. D. HAUSER
Probing the Evolutionary Origins of Music Perception
Ann. N.Y. Acad. Sci., December 1, 2005; 1060(1): 6 - 16.
[Abstract] [Full Text] [PDF]


Home page
Cereb CortexHome page
M. Steinschneider, I. O. Volkov, Y. I. Fishman, H. Oya, J. C. Arezzo, and M. A. Howard III
Intracortical Responses in Human and Monkey Primary Auditory Cortex Support a Temporal Processing Mechanism for Encoding of the Voice Onset Time Phonetic Parameter
Cereb Cortex, February 1, 2005; 15(2): 170 - 186.
[Abstract] [Full Text] [PDF]


Home page
NeurologyHome page
C. Carlson and E. K. St. Louis
Vacuum cleaner epilepsy
Neurology, July 13, 2004; 63(1): 190 - 191.
[Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Visit Other APS Journals Online