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Congenital Deafness Leads to Altered Overt Oculomotor Behaviors.

Author(s): Sharp A, Turgeon C, Johnson AP, Pannasch S, Champoux F, Ellemberg D

Front Neurosci. 2020;14:273 Authors: Sharp A, Turgeon C, Johnson AP, Pannasch S, Champoux F, Ellemberg D

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Inferior Longitudinal Fasciculus' Role in Visual Processing and Language Comprehension: A Combined MEG-DTI Study.

Author(s): Shin J, Rowley J, Chowdhury R, Jolicoeur P, Klein D, Grova C, Rosa-Neto P, Kobayashi E

Front Neurosci. 2019;13:875 Authors: Shin J, Rowley J, Chowdhury R, Jolicoeur P, Klein D, Grova C, Rosa-Neto P, Kobayashi E

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Aromatization Is Not Required for the Facilitation of Appetitive Sexual Behaviors in Ovariectomized Rats Treated With Estradiol and Testosterone.

Author(s): Jones SL, Rosenbaum S, Gardner Gregory J, Pfaus JG

Front Neurosci. 2019;13:798 Authors: Jones SL, Rosenbaum S, Gardner Gregory J, Pfaus JG

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Processing of Acoustic Information in Lexical Tone Production and Perception by Pediatric Cochlear Implant Recipients.

Author(s): Deroche MLD, Lu HP, Lin YS, Chatterjee M, Peng SC

Front Neurosci. 2019;13:639 Authors: Deroche MLD, Lu HP, Lin YS, Chatterjee M, Peng SC

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Influence of Head Tissue Conductivity Uncertainties on EEG Dipole Reconstruction.

Author(s): Vorwerk J, Aydin Ü, Wolters CH, Butson CR

Front Neurosci. 2019;13:531 Authors: Vorwerk J, Aydin Ü, Wolters CH, Butson CR

Article GUID: 31231178

Partially Overlapping Brain Networks for Singing and Cello Playing.

Author(s): Segado M, Hollinger A, Thibodeau J, Penhune V, Zatorre RJ

Front Neurosci. 2018;12:351 Authors: Segado M, Hollinger A, Thibodeau J, Penhune V, Zatorre RJ

Article GUID: 29892211

Integrated fMRI Preprocessing Framework Using Extended Kalman Filter for Estimation of Slice-Wise Motion.

Author(s): Pinsard B, Boutin A, Doyon J, Benali H

Front Neurosci. 2018;12:268 Authors: Pinsard B, Boutin A, Doyon J, Benali H

Article GUID: 29755312

Detection of abnormal resting-state networks in individual patients suffering from focal epilepsy: an initial step toward individual connectivity assessment.

Author(s): Dansereau CL, Bellec P, Lee K, Pittau F, Gotman J, Grova C

Front Neurosci. 2014;8:419 Authors: Dansereau CL, Bellec P, Lee K, Pittau F, Gotman J, Grova C

Article GUID: 25565949

The Music-In-Noise Task (MINT): A Tool for Dissecting Complex Auditory Perception.

Author(s): Coffey EBJ, Arseneau-Bruneau I, Zhang X, Zatorre RJ

Front Neurosci. 2019;13:199 Authors: Coffey EBJ, Arseneau-Bruneau I, Zhang X, Zatorre RJ

Article GUID: 30930734


Title:Partially Overlapping Brain Networks for Singing and Cello Playing.
Authors:Segado MHollinger AThibodeau JPenhune VZatorre RJ
Link:https://www.ncbi.nlm.nih.gov/pubmed/29892211?dopt=Abstract
DOI:10.3389/fnins.2018.00351
Category:Front Neurosci
PMID:29892211
Dept Affiliation: PSYCHOLOGY
1 Montreal Neurological Institute, Montreal, QC, Canada.
2 BRAMS International Laboratory for Brain, Music, and Sound Research, Montreal, QC, Canada.
3 Centre for Interdisciplinary Research in Music Media and Technology, Montreal, QC, Canada.
4 Department of Psychology, Concordia University, Montreal, QC, Canada.

Description:

Partially Overlapping Brain Networks for Singing and Cello Playing.

Front Neurosci. 2018;12:351

Authors: Segado M, Hollinger A, Thibodeau J, Penhune V, Zatorre RJ

Abstract

This research uses an MR-Compatible cello to compare functional brain activation during singing and cello playing within the same individuals to determine the extent to which arbitrary auditory-motor associations, like those required to play the cello, co-opt functional brain networks that evolved for singing. Musical instrument playing and singing both require highly specific associations between sounds and movements. Because these are both used to produce musical sounds, it is often assumed in the literature that their neural underpinnings are highly similar. However, singing is an evolutionarily old human trait, and the auditory-motor associations used for singing are also used for speech and non-speech vocalizations. This sets it apart from the arbitrary auditory-motor associations required to play musical instruments. The pitch range of the cello is similar to that of the human voice, but cello playing is completely independent of the vocal apparatus, and can therefore be used to dissociate the auditory-vocal network from that of the auditory-motor network. While in the MR-Scanner, 11 expert cellists listened to and subsequently produced individual tones either by singing or cello playing. All participants were able to sing and play the target tones in tune (<50C deviation from target). We found that brain activity during cello playing directly overlaps with brain activity during singing in many areas within the auditory-vocal network. These include primary motor, dorsal pre-motor, and supplementary motor cortices (M1, dPMC, SMA),the primary and periprimary auditory cortices within the superior temporal gyrus (STG) including Heschl's gyrus, anterior insula (aINS), anterior cingulate cortex (ACC), and intraparietal sulcus (IPS), and Cerebellum but, notably, exclude the periaqueductal gray (PAG) and basal ganglia (Putamen). Second, we found that activity within the overlapping areas is positively correlated with, and therefore likely contributing to, both singing and playing in tune determined with performance measures. Third, we found that activity in auditory areas is functionally connected with activity in dorsal motor and pre-motor areas, and that the connectivity between them is positively correlated with good performance on this task. This functional connectivity suggests that the brain areas are working together to contribute to task performance and not just coincidently active. Last, our findings showed that cello playing may directly co-opt vocal areas (including larynx area of motor cortex), especially if musical training begins before age 7.

PMID: 29892211 [PubMed]