Multisensory interactions between auditory and haptic object recognition.
Identifieur interne : 000C10 ( PubMed/Corpus ); précédent : 000C09; suivant : 000C11Multisensory interactions between auditory and haptic object recognition.
Auteurs : Tanja Kassuba ; Mareike M. Menz ; Brigitte Röder ; Hartwig R. SiebnerSource :
- Cerebral cortex (New York, N.Y. : 1991) [ 1460-2199 ] ; 2013.
English descriptors
- KwdEn :
- Adult, Auditory Perception (physiology), Brain Mapping, Cerebral Cortex (physiology), Decision Making (physiology), Female, Humans, Male, Nerve Net (physiology), Pattern Recognition, Physiological (physiology), Perceptual Masking (physiology), Recognition (Psychology) (physiology), Touch (physiology), Young Adult.
- MESH :
Abstract
Object manipulation produces characteristic sounds and causes specific haptic sensations that facilitate the recognition of the manipulated object. To identify the neural correlates of audio-haptic binding of object features, healthy volunteers underwent functional magnetic resonance imaging while they matched a target object to a sample object within and across audition and touch. By introducing a delay between the presentation of sample and target stimuli, it was possible to dissociate haptic-to-auditory and auditory-to-haptic matching. We hypothesized that only semantically coherent auditory and haptic object features activate cortical regions that host unified conceptual object representations. The left fusiform gyrus (FG) and posterior superior temporal sulcus (pSTS) showed increased activation during crossmodal matching of semantically congruent but not incongruent object stimuli. In the FG, this effect was found for haptic-to-auditory and auditory-to-haptic matching, whereas the pSTS only displayed a crossmodal matching effect for congruent auditory targets. Auditory and somatosensory association cortices showed increased activity during crossmodal object matching which was, however, independent of semantic congruency. Together, the results show multisensory interactions at different hierarchical stages of auditory and haptic object processing. Object-specific crossmodal interactions culminate in the left FG, which may provide a higher order convergence zone for conceptual object knowledge.
DOI: 10.1093/cercor/bhs076
PubMed: 22518017
Links to Exploration step
pubmed:22518017Le document en format XML
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Siebner</name></author></titleStmt><publicationStmt><idno type="wicri:source">PubMed</idno><date when="2013">2013</date><idno type="doi">10.1093/cercor/bhs076</idno><idno type="RBID">pubmed:22518017</idno><idno type="pmid">22518017</idno><idno type="wicri:Area/PubMed/Corpus">000C10</idno></publicationStmt><sourceDesc><biblStruct><analytic><title xml:lang="en">Multisensory interactions between auditory and haptic object recognition.</title><author><name sortKey="Kassuba, Tanja" sort="Kassuba, Tanja" uniqKey="Kassuba T" first="Tanja" last="Kassuba">Tanja Kassuba</name><affiliation><nlm:affiliation>Danish Research Centre for Magnetic Resonance, Copenhagen University Hospital Hvidovre, 2650 Hvidovre, Denmark. tanjak@drcmr.dk</nlm:affiliation></affiliation></author><author><name sortKey="Menz, Mareike M" sort="Menz, Mareike M" uniqKey="Menz M" first="Mareike M" last="Menz">Mareike M. Menz</name></author><author><name sortKey="Roder, Brigitte" sort="Roder, Brigitte" uniqKey="Roder B" first="Brigitte" last="Röder">Brigitte Röder</name></author><author><name sortKey="Siebner, Hartwig R" sort="Siebner, Hartwig R" uniqKey="Siebner H" first="Hartwig R" last="Siebner">Hartwig R. Siebner</name></author></analytic><series><title level="j">Cerebral cortex (New York, N.Y. : 1991)</title><idno type="eISSN">1460-2199</idno><imprint><date when="2013" type="published">2013</date></imprint></series></biblStruct></sourceDesc></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Adult</term><term>Auditory Perception (physiology)</term><term>Brain Mapping</term><term>Cerebral Cortex (physiology)</term><term>Decision Making (physiology)</term><term>Female</term><term>Humans</term><term>Male</term><term>Nerve Net (physiology)</term><term>Pattern Recognition, Physiological (physiology)</term><term>Perceptual Masking (physiology)</term><term>Recognition (Psychology) (physiology)</term><term>Touch (physiology)</term><term>Young Adult</term></keywords><keywords scheme="MESH" qualifier="physiology" xml:lang="en"><term>Auditory Perception</term><term>Cerebral Cortex</term><term>Decision Making</term><term>Nerve Net</term><term>Pattern Recognition, Physiological</term><term>Perceptual Masking</term><term>Recognition (Psychology)</term><term>Touch</term></keywords><keywords scheme="MESH" xml:lang="en"><term>Adult</term><term>Brain Mapping</term><term>Female</term><term>Humans</term><term>Male</term><term>Young Adult</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">Object manipulation produces characteristic sounds and causes specific haptic sensations that facilitate the recognition of the manipulated object. To identify the neural correlates of audio-haptic binding of object features, healthy volunteers underwent functional magnetic resonance imaging while they matched a target object to a sample object within and across audition and touch. By introducing a delay between the presentation of sample and target stimuli, it was possible to dissociate haptic-to-auditory and auditory-to-haptic matching. We hypothesized that only semantically coherent auditory and haptic object features activate cortical regions that host unified conceptual object representations. The left fusiform gyrus (FG) and posterior superior temporal sulcus (pSTS) showed increased activation during crossmodal matching of semantically congruent but not incongruent object stimuli. In the FG, this effect was found for haptic-to-auditory and auditory-to-haptic matching, whereas the pSTS only displayed a crossmodal matching effect for congruent auditory targets. Auditory and somatosensory association cortices showed increased activity during crossmodal object matching which was, however, independent of semantic congruency. Together, the results show multisensory interactions at different hierarchical stages of auditory and haptic object processing. Object-specific crossmodal interactions culminate in the left FG, which may provide a higher order convergence zone for conceptual object knowledge.</div></front></TEI><pubmed><MedlineCitation Owner="NLM" Status="MEDLINE"><PMID Version="1">22518017</PMID><DateCreated><Year>2013</Year><Month>04</Month><Day>04</Day></DateCreated><DateCompleted><Year>2013</Year><Month>09</Month><Day>30</Day></DateCompleted><Article PubModel="Print-Electronic"><Journal><ISSN IssnType="Electronic">1460-2199</ISSN><JournalIssue CitedMedium="Internet"><Volume>23</Volume><Issue>5</Issue><PubDate><Year>2013</Year><Month>May</Month></PubDate></JournalIssue><Title>Cerebral cortex (New York, N.Y. : 1991)</Title><ISOAbbreviation>Cereb. Cortex</ISOAbbreviation></Journal><ArticleTitle>Multisensory interactions between auditory and haptic object recognition.</ArticleTitle><Pagination><MedlinePgn>1097-107</MedlinePgn></Pagination><ELocationID EIdType="doi" ValidYN="Y">10.1093/cercor/bhs076</ELocationID><Abstract><AbstractText>Object manipulation produces characteristic sounds and causes specific haptic sensations that facilitate the recognition of the manipulated object. To identify the neural correlates of audio-haptic binding of object features, healthy volunteers underwent functional magnetic resonance imaging while they matched a target object to a sample object within and across audition and touch. By introducing a delay between the presentation of sample and target stimuli, it was possible to dissociate haptic-to-auditory and auditory-to-haptic matching. We hypothesized that only semantically coherent auditory and haptic object features activate cortical regions that host unified conceptual object representations. The left fusiform gyrus (FG) and posterior superior temporal sulcus (pSTS) showed increased activation during crossmodal matching of semantically congruent but not incongruent object stimuli. In the FG, this effect was found for haptic-to-auditory and auditory-to-haptic matching, whereas the pSTS only displayed a crossmodal matching effect for congruent auditory targets. Auditory and somatosensory association cortices showed increased activity during crossmodal object matching which was, however, independent of semantic congruency. Together, the results show multisensory interactions at different hierarchical stages of auditory and haptic object processing. Object-specific crossmodal interactions culminate in the left FG, which may provide a higher order convergence zone for conceptual object knowledge.</AbstractText></Abstract><AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Kassuba</LastName><ForeName>Tanja</ForeName><Initials>T</Initials><AffiliationInfo><Affiliation>Danish Research Centre for Magnetic Resonance, Copenhagen University Hospital Hvidovre, 2650 Hvidovre, Denmark. tanjak@drcmr.dk</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Menz</LastName><ForeName>Mareike M</ForeName><Initials>MM</Initials></Author><Author ValidYN="Y"><LastName>Röder</LastName><ForeName>Brigitte</ForeName><Initials>B</Initials></Author><Author ValidYN="Y"><LastName>Siebner</LastName><ForeName>Hartwig R</ForeName><Initials>HR</Initials></Author></AuthorList><Language>eng</Language><PublicationTypeList><PublicationType UI="D016428">Journal Article</PublicationType><PublicationType UI="D013485">Research Support, Non-U.S. Gov't</PublicationType></PublicationTypeList><ArticleDate DateType="Electronic"><Year>2012</Year><Month>04</Month><Day>19</Day></ArticleDate></Article><MedlineJournalInfo><Country>United States</Country><MedlineTA>Cereb Cortex</MedlineTA><NlmUniqueID>9110718</NlmUniqueID><ISSNLinking>1047-3211</ISSNLinking></MedlineJournalInfo><CitationSubset>IM</CitationSubset><MeshHeadingList><MeshHeading><DescriptorName MajorTopicYN="N" UI="D000328">Adult</DescriptorName></MeshHeading><MeshHeading><DescriptorName MajorTopicYN="N" UI="D001307">Auditory Perception</DescriptorName><QualifierName MajorTopicYN="Y" UI="Q000502">physiology</QualifierName></MeshHeading><MeshHeading><DescriptorName MajorTopicYN="N" UI="D001931">Brain Mapping</DescriptorName></MeshHeading><MeshHeading><DescriptorName MajorTopicYN="N" UI="D002540">Cerebral Cortex</DescriptorName><QualifierName MajorTopicYN="Y" UI="Q000502">physiology</QualifierName></MeshHeading><MeshHeading><DescriptorName MajorTopicYN="N" UI="D003657">Decision Making</DescriptorName><QualifierName MajorTopicYN="Y" UI="Q000502">physiology</QualifierName></MeshHeading><MeshHeading><DescriptorName MajorTopicYN="N" UI="D005260">Female</DescriptorName></MeshHeading><MeshHeading><DescriptorName MajorTopicYN="N" UI="D006801">Humans</DescriptorName></MeshHeading><MeshHeading><DescriptorName MajorTopicYN="N" UI="D008297">Male</DescriptorName></MeshHeading><MeshHeading><DescriptorName MajorTopicYN="N" UI="D009415">Nerve Net</DescriptorName><QualifierName MajorTopicYN="N" UI="Q000502">physiology</QualifierName></MeshHeading><MeshHeading><DescriptorName MajorTopicYN="N" UI="D046709">Pattern Recognition, Physiological</DescriptorName><QualifierName MajorTopicYN="Y" UI="Q000502">physiology</QualifierName></MeshHeading><MeshHeading><DescriptorName MajorTopicYN="N" UI="D010470">Perceptual Masking</DescriptorName><QualifierName MajorTopicYN="Y" UI="Q000502">physiology</QualifierName></MeshHeading><MeshHeading><DescriptorName MajorTopicYN="N" UI="D021641">Recognition (Psychology)</DescriptorName><QualifierName MajorTopicYN="Y" UI="Q000502">physiology</QualifierName></MeshHeading><MeshHeading><DescriptorName MajorTopicYN="N" UI="D014110">Touch</DescriptorName><QualifierName MajorTopicYN="Y" UI="Q000502">physiology</QualifierName></MeshHeading><MeshHeading><DescriptorName MajorTopicYN="N" UI="D055815">Young Adult</DescriptorName></MeshHeading></MeshHeadingList></MedlineCitation><PubmedData><History><PubMedPubDate PubStatus="aheadofprint"><Year>2012</Year><Month>4</Month><Day>19</Day></PubMedPubDate><PubMedPubDate PubStatus="entrez"><Year>2012</Year><Month>4</Month><Day>21</Day><Hour>6</Hour><Minute>0</Minute></PubMedPubDate><PubMedPubDate PubStatus="pubmed"><Year>2012</Year><Month>4</Month><Day>21</Day><Hour>6</Hour><Minute>0</Minute></PubMedPubDate><PubMedPubDate PubStatus="medline"><Year>2013</Year><Month>10</Month><Day>1</Day><Hour>6</Hour><Minute>0</Minute></PubMedPubDate></History><PublicationStatus>ppublish</PublicationStatus><ArticleIdList><ArticleId IdType="pii">bhs076</ArticleId><ArticleId IdType="doi">10.1093/cercor/bhs076</ArticleId><ArticleId IdType="pubmed">22518017</ArticleId></ArticleIdList></PubmedData></pubmed></record>Pour manipuler ce document sous Unix (Dilib)
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