Tight covariation of BOLD signal changes and slow ERPs in the parietal cortex in a parametric spatial imagery task with haptic acquisition
Identifieur interne : 000F72 ( Istex/Corpus ); précédent : 000F71; suivant : 000F73Tight covariation of BOLD signal changes and slow ERPs in the parietal cortex in a parametric spatial imagery task with haptic acquisition
Auteurs : Tobias Schicke ; Lars Muckli ; Anton L. Beer ; Michael Wibral ; Wolf Singer ; Rainer Goebel ; Frank Rösler ; Brigitte RöderSource :
- European Journal of Neuroscience [ 0953-816X ] ; 2006-04.
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Abstract
The present study investigated the relation of brain activity patterns measured with functional magnetic resonance imaging (fMRI) and slow event‐related potentials (ERPs) associated with a complex cognitive task. A second goal was to examine the neural correlates of spatial imagery of haptically – instead of visually – acquired representations. Using a mental image scanning task, spatial imagery requirements were systematically manipulated by parametrically varying the distance between haptically acquired landmarks. Results showed a close relation between slow ERPs and the blood oxygenation level dependent (BOLD) signal in human parietal lobe. Reaction times of mental scanning correlated with the distances between landmarks on the learned display. In parallel, duration and amplitude of slow ERPs and duration of the haemodynamic response systematically varied as a function of mental scanning distance. Source analysis confirmed that the ERP imagery effect likely originated from the same cortical substrate as the corresponding BOLD effect. This covariation of the BOLD signal with slow ERPs is in line with recent findings in animals demonstrating a tight link between local field potentials and the BOLD signal. The parietal location of the imagery effect is consistent with the idea that externally triggered (perceptual) and mentally driven (imagery) spatial processes are both mediated by the same supramodal brain areas.
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DOI: 10.1111/j.1460-9568.2006.04720.x
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ISTEX:5E9705143B48FA9F1219953A0483F5EC062D9714Le document en format XML
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Beer</name><affiliation><mods:affiliation>Department of Psychology, Boston University, Boston, United States</mods:affiliation></affiliation></author><author><name sortKey="Wibral, Michael" sort="Wibral, Michael" uniqKey="Wibral M" first="Michael" last="Wibral">Michael Wibral</name><affiliation><mods:affiliation>Max Planck Institute for Brain Research, Frankfurt/Main, Germany</mods:affiliation></affiliation><affiliation><mods:affiliation>Brain Imaging Center Frankfurt, Frankfurt/Main, Germany</mods:affiliation></affiliation></author><author><name sortKey="Singer, Wolf" sort="Singer, Wolf" uniqKey="Singer W" first="Wolf" last="Singer">Wolf Singer</name><affiliation><mods:affiliation>Max Planck Institute for Brain Research, Frankfurt/Main, Germany</mods:affiliation></affiliation><affiliation><mods:affiliation>Brain Imaging Center Frankfurt, Frankfurt/Main, Germany</mods:affiliation></affiliation></author><author><name sortKey="Goebel, Rainer" sort="Goebel, Rainer" uniqKey="Goebel R" first="Rainer" last="Goebel">Rainer Goebel</name><affiliation><mods:affiliation>Faculty of Psychology, Maastricht University, Maastricht, Netherlands</mods:affiliation></affiliation></author><author><name sortKey="Rosler, Frank" sort="Rosler, Frank" uniqKey="Rosler F" first="Frank" last="Rösler">Frank Rösler</name><affiliation><mods:affiliation>Department of Psychology, Philipps‐University Marburg, Marburg, Germany</mods:affiliation></affiliation></author><author><name sortKey="Roder, Brigitte" sort="Roder, Brigitte" uniqKey="Roder B" first="Brigitte" last="Röder">Brigitte Röder</name><affiliation><mods:affiliation>Biological Psychology and Neuropsychology, University of Hamburg, D‐20146 Hamburg, Germany</mods:affiliation></affiliation></author></analytic><monogr></monogr><series><title level="j">European Journal of Neuroscience</title><idno type="ISSN">0953-816X</idno><idno type="eISSN">1460-9568</idno><imprint><publisher>Blackwell Publishing Ltd</publisher><pubPlace>Oxford, UK</pubPlace><date type="published" when="2006-04">2006-04</date><biblScope unit="volume">23</biblScope><biblScope unit="issue">7</biblScope><biblScope unit="page" from="1910">1910</biblScope><biblScope unit="page" to="1918">1918</biblScope></imprint><idno type="ISSN">0953-816X</idno></series><idno type="istex">5E9705143B48FA9F1219953A0483F5EC062D9714</idno><idno type="DOI">10.1111/j.1460-9568.2006.04720.x</idno><idno type="ArticleID">EJN4720</idno></biblStruct></sourceDesc><seriesStmt><idno type="ISSN">0953-816X</idno></seriesStmt></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>cortex</term><term>event‐related potentials</term><term>fMRI</term><term>human</term><term>mental imagery</term><term>source modelling</term></keywords></textClass><langUsage><language ident="en">en</language></langUsage></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">The present study investigated the relation of brain activity patterns measured with functional magnetic resonance imaging (fMRI) and slow event‐related potentials (ERPs) associated with a complex cognitive task. A second goal was to examine the neural correlates of spatial imagery of haptically – instead of visually – acquired representations. Using a mental image scanning task, spatial imagery requirements were systematically manipulated by parametrically varying the distance between haptically acquired landmarks. Results showed a close relation between slow ERPs and the blood oxygenation level dependent (BOLD) signal in human parietal lobe. Reaction times of mental scanning correlated with the distances between landmarks on the learned display. In parallel, duration and amplitude of slow ERPs and duration of the haemodynamic response systematically varied as a function of mental scanning distance. Source analysis confirmed that the ERP imagery effect likely originated from the same cortical substrate as the corresponding BOLD effect. This covariation of the BOLD signal with slow ERPs is in line with recent findings in animals demonstrating a tight link between local field potentials and the BOLD signal. The parietal location of the imagery effect is consistent with the idea that externally triggered (perceptual) and mentally driven (imagery) spatial processes are both mediated by the same supramodal brain areas.</div></front></TEI><istex><corpusName>wiley</corpusName><author><json:item><name>Tobias Schicke</name><affiliations><json:string>Biological Psychology and Neuropsychology, University of Hamburg, D‐20146 Hamburg, Germany</json:string></affiliations></json:item><json:item><name>Lars Muckli</name><affiliations><json:string>Max Planck Institute for Brain Research, Frankfurt/Main, Germany</json:string><json:string>Brain Imaging Center Frankfurt, Frankfurt/Main, Germany</json:string></affiliations></json:item><json:item><name>Anton L. 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A second goal was to examine the neural correlates of spatial imagery of haptically – instead of visually – acquired representations. Using a mental image scanning task, spatial imagery requirements were systematically manipulated by parametrically varying the distance between haptically acquired landmarks. Results showed a close relation between slow ERPs and the blood oxygenation level dependent (BOLD) signal in human parietal lobe. Reaction times of mental scanning correlated with the distances between landmarks on the learned display. In parallel, duration and amplitude of slow ERPs and duration of the haemodynamic response systematically varied as a function of mental scanning distance. Source analysis confirmed that the ERP imagery effect likely originated from the same cortical substrate as the corresponding BOLD effect. 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contributed equally to this work.</note><affiliation>T.S. and L.M. contributed equally to this work.</affiliation><affiliation>Max Planck Institute for Brain Research, Frankfurt/Main, Germany</affiliation><affiliation>Brain Imaging Center Frankfurt, Frankfurt/Main, Germany</affiliation></author><author><persName><forename type="first">Anton L.</forename><surname>Beer</surname></persName><affiliation>Department of Psychology, Boston University, Boston, United States</affiliation></author><author><persName><forename type="first">Michael</forename><surname>Wibral</surname></persName><affiliation>Max Planck Institute for Brain Research, Frankfurt/Main, Germany</affiliation><affiliation>Brain Imaging Center Frankfurt, Frankfurt/Main, Germany</affiliation></author><author><persName><forename type="first">Wolf</forename><surname>Singer</surname></persName><affiliation>Max Planck Institute for Brain Research, Frankfurt/Main, Germany</affiliation><affiliation>Brain Imaging Center Frankfurt, 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when="2006-04"></date><biblScope unit="volume">23</biblScope><biblScope unit="issue">7</biblScope><biblScope unit="page" from="1910">1910</biblScope><biblScope unit="page" to="1918">1918</biblScope></imprint></monogr><idno type="istex">5E9705143B48FA9F1219953A0483F5EC062D9714</idno><idno type="DOI">10.1111/j.1460-9568.2006.04720.x</idno><idno type="ArticleID">EJN4720</idno></biblStruct></sourceDesc></fileDesc><profileDesc><creation><date>2006</date></creation><langUsage><language ident="en">en</language></langUsage><abstract xml:lang="en"><p>The present study investigated the relation of brain activity patterns measured with functional magnetic resonance imaging (fMRI) and slow event‐related potentials (ERPs) associated with a complex cognitive task. A second goal was to examine the neural correlates of spatial imagery of haptically – instead of visually – acquired representations. Using a mental image scanning task, spatial imagery requirements were systematically manipulated by parametrically varying the distance between haptically acquired landmarks. Results showed a close relation between slow ERPs and the blood oxygenation level dependent (BOLD) signal in human parietal lobe. Reaction times of mental scanning correlated with the distances between landmarks on the learned display. In parallel, duration and amplitude of slow ERPs and duration of the haemodynamic response systematically varied as a function of mental scanning distance. Source analysis confirmed that the ERP imagery effect likely originated from the same cortical substrate as the corresponding BOLD effect. This covariation of the BOLD signal with slow ERPs is in line with recent findings in animals demonstrating a tight link between local field potentials and the BOLD signal. The parietal location of the imagery effect is consistent with the idea that externally triggered (perceptual) and mentally driven (imagery) spatial processes are both mediated by the same supramodal brain areas.</p></abstract><textClass xml:lang="en"><keywords scheme="keyword"><list><head>keywords</head><item><term>cortex</term></item><item><term>event‐related potentials</term></item><item><term>fMRI</term></item><item><term>mental imagery</term></item><item><term>human</term></item><item><term>source modelling</term></item></list></keywords></textClass></profileDesc><revisionDesc><change when="2006-04">Published</change></revisionDesc></teiHeader></istex:fulltextTEI><json:item><original>false</original><mimetype>text/plain</mimetype><extension>txt</extension><uri>https://api.istex.fr/document/5E9705143B48FA9F1219953A0483F5EC062D9714/fulltext/txt</uri></json:item></fulltext><metadata><istex:metadataXml wicri:clean="Wiley, elements deleted: body"><istex:xmlDeclaration>version="1.0" encoding="UTF-8" standalone="yes"</istex:xmlDeclaration><istex:document><component version="2.0" type="serialArticle" xml:lang="en"><header><publicationMeta level="product"><publisherInfo><publisherName>Blackwell Publishing Ltd</publisherName><publisherLoc>Oxford, UK</publisherLoc></publisherInfo><doi origin="wiley" registered="yes">10.1111/(ISSN)1460-9568</doi><issn type="print">0953-816X</issn><issn type="electronic">1460-9568</issn><idGroup><id type="product" value="EJN"></id><id type="publisherDivision" value="ST"></id></idGroup><titleGroup><title type="main" sort="EUROPEAN JOURNAL OF NEUROSCIENCE">European Journal of Neuroscience</title></titleGroup></publicationMeta><publicationMeta level="part" position="04107"><doi origin="wiley">10.1111/ejn.2006.23.issue-7</doi><numberingGroup><numbering type="journalVolume" number="23">23</numbering><numbering type="journalIssue" number="7">7</numbering></numberingGroup><coverDate startDate="2006-04">April 2006</coverDate></publicationMeta><publicationMeta level="unit" type="article" position="24" status="forIssue"><doi origin="wiley">10.1111/j.1460-9568.2006.04720.x</doi><idGroup><id type="unit" value="EJN4720"></id></idGroup><countGroup><count type="pageTotal" number="9"></count></countGroup><titleGroup><title type="tocHeading1">Research Reports</title></titleGroup><eventGroup><event type="firstOnline" date="2006-04-05"></event><event type="publishedOnlineFinalForm" date="2006-04-05"></event><event type="xmlConverted" agent="Converter:BPG_TO_WML3G version:3.2.2 mode:FullText" date="2013-07-16"></event><event type="xmlConverted" agent="Converter:WILEY_ML3G_TO_WILEY_ML3GV2 version:4.0.1" date="2014-03-12"></event><event type="xmlConverted" agent="Converter:WML3G_To_WML3G version:4.1.7 mode:FullText,remove_FC" date="2014-10-16"></event></eventGroup><numberingGroup><numbering type="pageFirst" number="1910">1910</numbering><numbering type="pageLast" number="1918">1918</numbering></numberingGroup><correspondenceTo>Tobias Schicke, as above.
E‐mail: <email normalForm="tobias.schicke@uni-hamburg.de">tobias.schicke@uni‐hamburg.de</email></correspondenceTo><linkGroup><link type="toTypesetVersion" href="file:EJN.EJN4720.pdf"></link></linkGroup></publicationMeta><contentMeta><unparsedEditorialHistory>Received 29 September 2005, revised 25 January 2006, accepted 31 January 2006</unparsedEditorialHistory><countGroup><count type="figureTotal" number="4"></count><count type="tableTotal" number="3"></count><count type="formulaTotal" number="0"></count><count type="referenceTotal" number="44"></count><count type="wordTotal" number="7192"></count><count type="linksPubMed" number="0"></count><count type="linksCrossRef" number="0"></count></countGroup><titleGroup><title type="main">Tight covariation of BOLD signal changes and slow ERPs in the parietal cortex in a parametric spatial imagery task with haptic acquisition</title><title type="shortAuthors">T. Schicke <i>et al</i>.</title><title type="short">Covariaton of BOLD signal and slow ERPs</title></titleGroup><creators><creator creatorRole="author" xml:id="cr1" affiliationRef="#a1" noteRef="#fn1"><personName><givenNames>Tobias</givenNames><familyName>Schicke</familyName></personName></creator><creator creatorRole="author" xml:id="cr2" affiliationRef="#a2 #a3" noteRef="#fn1"><personName><givenNames>Lars</givenNames><familyName>Muckli</familyName></personName></creator><creator creatorRole="author" xml:id="cr3" affiliationRef="#a4"><personName><givenNames>Anton L.</givenNames><familyName>Beer</familyName></personName></creator><creator creatorRole="author" xml:id="cr4" affiliationRef="#a2 #a3"><personName><givenNames>Michael</givenNames><familyName>Wibral</familyName></personName></creator><creator creatorRole="author" xml:id="cr5" affiliationRef="#a2 #a3"><personName><givenNames>Wolf</givenNames><familyName>Singer</familyName></personName></creator><creator creatorRole="author" xml:id="cr6" affiliationRef="#a5"><personName><givenNames>Rainer</givenNames><familyName>Goebel</familyName></personName></creator><creator creatorRole="author" xml:id="cr7" affiliationRef="#a6"><personName><givenNames>Frank</givenNames><familyName>Rösler</familyName></personName></creator><creator creatorRole="author" xml:id="cr8" affiliationRef="#a1"><personName><givenNames>Brigitte</givenNames><familyName>Röder</familyName></personName></creator></creators><affiliationGroup><affiliation xml:id="a1" countryCode="DE"><unparsedAffiliation>Biological Psychology and Neuropsychology, University of Hamburg, D‐20146 Hamburg, Germany</unparsedAffiliation></affiliation><affiliation xml:id="a2" countryCode="DE"><unparsedAffiliation>Max Planck Institute for Brain Research, Frankfurt/Main, Germany</unparsedAffiliation></affiliation><affiliation xml:id="a3" countryCode="DE"><unparsedAffiliation>Brain Imaging Center Frankfurt, Frankfurt/Main, Germany</unparsedAffiliation></affiliation><affiliation xml:id="a4" countryCode="US"><unparsedAffiliation>Department of Psychology, Boston University, Boston, United States</unparsedAffiliation></affiliation><affiliation xml:id="a5" countryCode="NL"><unparsedAffiliation>Faculty of Psychology, Maastricht University, Maastricht, Netherlands</unparsedAffiliation></affiliation><affiliation xml:id="a6" countryCode="DE"><unparsedAffiliation>Department of Psychology, Philipps‐University Marburg, Marburg, Germany</unparsedAffiliation></affiliation></affiliationGroup><keywordGroup xml:lang="en"><keyword xml:id="k1">cortex</keyword><keyword xml:id="k2">event‐related potentials</keyword><keyword xml:id="k3">fMRI</keyword><keyword xml:id="k4">mental imagery</keyword><keyword xml:id="k5">human</keyword><keyword xml:id="k6">source modelling</keyword></keywordGroup><abstractGroup><abstract type="main" xml:lang="en"><title type="main">Abstract</title><p>The present study investigated the relation of brain activity patterns measured with functional magnetic resonance imaging (fMRI) and slow event‐related potentials (ERPs) associated with a complex cognitive task. A second goal was to examine the neural correlates of spatial imagery of haptically – instead of visually – acquired representations. Using a mental image scanning task, spatial imagery requirements were systematically manipulated by parametrically varying the distance between haptically acquired landmarks. Results showed a close relation between slow ERPs and the blood oxygenation level dependent (BOLD) signal in human parietal lobe. Reaction times of mental scanning correlated with the distances between landmarks on the learned display. In parallel, duration and amplitude of slow ERPs and duration of the haemodynamic response systematically varied as a function of mental scanning distance. Source analysis confirmed that the ERP imagery effect likely originated from the same cortical substrate as the corresponding BOLD effect. This covariation of the BOLD signal with slow ERPs is in line with recent findings in animals demonstrating a tight link between local field potentials and the BOLD signal. The parietal location of the imagery effect is consistent with the idea that externally triggered (perceptual) and mentally driven (imagery) spatial processes are both mediated by the same supramodal brain areas.</p></abstract></abstractGroup></contentMeta><noteGroup><note xml:id="fn1"><p> T.S. and L.M. contributed equally to this work.</p></note></noteGroup></header></component></istex:document></istex:metadataXml><mods version="3.6"><titleInfo lang="en"><title>Tight covariation of BOLD signal changes and slow ERPs in the parietal cortex in a parametric spatial imagery task with haptic acquisition</title></titleInfo><titleInfo type="abbreviated"><title>Covariaton of BOLD signal and slow ERPs</title></titleInfo><titleInfo type="alternative" contentType="CDATA" lang="en"><title>Tight covariation of BOLD signal changes and slow ERPs in the parietal cortex in a parametric spatial imagery task with haptic acquisition</title></titleInfo><name type="personal"><namePart type="given">Tobias</namePart><namePart type="family">Schicke</namePart><affiliation>Biological Psychology and Neuropsychology, University of Hamburg, D‐20146 Hamburg, Germany</affiliation><description>T.S. and L.M. contributed equally to this work.</description><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Lars</namePart><namePart type="family">Muckli</namePart><affiliation>Max Planck Institute for Brain Research, Frankfurt/Main, Germany</affiliation><affiliation>Brain Imaging Center Frankfurt, Frankfurt/Main, Germany</affiliation><description>T.S. and L.M. contributed equally to this work.</description><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Anton L.</namePart><namePart type="family">Beer</namePart><affiliation>Department of Psychology, Boston University, Boston, United States</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Michael</namePart><namePart type="family">Wibral</namePart><affiliation>Max Planck Institute for Brain Research, Frankfurt/Main, Germany</affiliation><affiliation>Brain Imaging Center Frankfurt, Frankfurt/Main, Germany</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Wolf</namePart><namePart type="family">Singer</namePart><affiliation>Max Planck Institute for Brain Research, Frankfurt/Main, Germany</affiliation><affiliation>Brain Imaging Center Frankfurt, Frankfurt/Main, Germany</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Rainer</namePart><namePart type="family">Goebel</namePart><affiliation>Faculty of Psychology, Maastricht University, Maastricht, Netherlands</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Frank</namePart><namePart type="family">Rösler</namePart><affiliation>Department of Psychology, Philipps‐University Marburg, Marburg, Germany</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Brigitte</namePart><namePart type="family">Röder</namePart><affiliation>Biological Psychology and Neuropsychology, University of Hamburg, D‐20146 Hamburg, Germany</affiliation><role><roleTerm type="text">author</roleTerm></role></name><typeOfResource>text</typeOfResource><genre type="article" displayLabel="article"></genre><originInfo><publisher>Blackwell Publishing Ltd</publisher><place><placeTerm type="text">Oxford, UK</placeTerm></place><dateIssued encoding="w3cdtf">2006-04</dateIssued><edition>Received 29 September 2005, revised 25 January 2006, accepted 31 January 2006</edition><copyrightDate encoding="w3cdtf">2006</copyrightDate></originInfo><language><languageTerm type="code" authority="rfc3066">en</languageTerm><languageTerm type="code" authority="iso639-2b">eng</languageTerm></language><physicalDescription><internetMediaType>text/html</internetMediaType><extent unit="figures">4</extent><extent unit="tables">3</extent><extent unit="references">44</extent><extent unit="words">7192</extent></physicalDescription><abstract lang="en">The present study investigated the relation of brain activity patterns measured with functional magnetic resonance imaging (fMRI) and slow event‐related potentials (ERPs) associated with a complex cognitive task. A second goal was to examine the neural correlates of spatial imagery of haptically – instead of visually – acquired representations. Using a mental image scanning task, spatial imagery requirements were systematically manipulated by parametrically varying the distance between haptically acquired landmarks. Results showed a close relation between slow ERPs and the blood oxygenation level dependent (BOLD) signal in human parietal lobe. Reaction times of mental scanning correlated with the distances between landmarks on the learned display. In parallel, duration and amplitude of slow ERPs and duration of the haemodynamic response systematically varied as a function of mental scanning distance. Source analysis confirmed that the ERP imagery effect likely originated from the same cortical substrate as the corresponding BOLD effect. This covariation of the BOLD signal with slow ERPs is in line with recent findings in animals demonstrating a tight link between local field potentials and the BOLD signal. The parietal location of the imagery effect is consistent with the idea that externally triggered (perceptual) and mentally driven (imagery) spatial processes are both mediated by the same supramodal brain areas.</abstract><subject lang="en"><genre>keywords</genre><topic>cortex</topic><topic>event‐related potentials</topic><topic>fMRI</topic><topic>mental imagery</topic><topic>human</topic><topic>source modelling</topic></subject><relatedItem type="host"><titleInfo><title>European Journal of Neuroscience</title></titleInfo><genre type="journal">journal</genre><identifier type="ISSN">0953-816X</identifier><identifier type="eISSN">1460-9568</identifier><identifier type="DOI">10.1111/(ISSN)1460-9568</identifier><identifier type="PublisherID">EJN</identifier><part><date>2006</date><detail type="volume"><caption>vol.</caption><number>23</number></detail><detail type="issue"><caption>no.</caption><number>7</number></detail><extent unit="pages"><start>1910</start><end>1918</end><total>9</total></extent></part></relatedItem><identifier type="istex">5E9705143B48FA9F1219953A0483F5EC062D9714</identifier><identifier type="DOI">10.1111/j.1460-9568.2006.04720.x</identifier><identifier type="ArticleID">EJN4720</identifier><recordInfo><recordContentSource>WILEY</recordContentSource><recordOrigin>Blackwell Publishing Ltd</recordOrigin></recordInfo></mods></metadata><serie></serie></istex></record>Pour manipuler ce document sous Unix (Dilib)
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