Neuroanatomical organization of the cholinergic system in the central nervous system of a basal actinopterygian fish, the senegal bichir Polypterus senegalus
Identifieur interne : 001535 ( Istex/Corpus ); précédent : 001534; suivant : 001536Neuroanatomical organization of the cholinergic system in the central nervous system of a basal actinopterygian fish, the senegal bichir Polypterus senegalus
Auteurs : Jesús M. L Pez ; Jorge Perlado ; Ruth Morona ; R. Glenn Northcutt ; Agustín GonzálezSource :
- Journal of Comparative Neurology [ 0021-9967 ] ; 2013-01-01.
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Abstract
Polypterid bony fishes are believed to be basal to other living ray‐finned fishes, and their brain organization is therefore critical in providing information as to primitive neural characters that existed in the earliest ray‐finned fishes. The cholinergic system has been characterized in more advanced ray‐finned fishes, but not in polypterids. In order to establish which cholinergic neural centers characterized the earliest ray‐finned fishes, the distribution of choline acetyltransferase (ChAT) is described in Polypterus and compared with the distribution of this molecule in other ray‐finned fishes. Cell groups immunoreactive for ChAT were observed in the hypothalamus, the habenula, the optic tectum, the isthmus, the cranial motor nuclei, and the spinal motor column. Cholinergic fibers were observed in both the telencephalic pallium and the subpallium, in the thalamus and pretectum, in the optic tectum and torus semicircularis, in the mesencephalic tegmentum, in the cerebellar crest, in the solitary nucleus, and in the dorsal column nuclei. Comparison of the data within a segmental neuromeric context indicates that the cholinergic system in polypterid fishes is generally similar to that in other ray‐finned fishes, but cholinergic‐positive neurons in the pallium and subpallium, and in the thalamus and cerebellum, of teleosts appear to have evolved following the separation of polypterids and other ray‐finned fishes. J. Comp. Neurol. 521:24–49, 2013. © 2012 Wiley Periodicals, Inc.
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DOI: 10.1002/cne.23155
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L Pez</name><affiliation><mods:affiliation>Department of Cell Biology, Faculty of Biology, University Complutense, 28040 Madrid, Spain</mods:affiliation></affiliation></author><author><name sortKey="Perlado, Jorge" sort="Perlado, Jorge" uniqKey="Perlado J" first="Jorge" last="Perlado">Jorge Perlado</name><affiliation><mods:affiliation>Department of Cell Biology, Faculty of Biology, University Complutense, 28040 Madrid, Spain</mods:affiliation></affiliation></author><author><name sortKey="Morona, Ruth" sort="Morona, Ruth" uniqKey="Morona R" first="Ruth" last="Morona">Ruth Morona</name><affiliation><mods:affiliation>Department of Cell Biology, Faculty of Biology, University Complutense, 28040 Madrid, Spain</mods:affiliation></affiliation></author><author><name sortKey="Northcutt, R Glenn" sort="Northcutt, R Glenn" uniqKey="Northcutt R" first="R. Glenn" last="Northcutt">R. Glenn Northcutt</name><affiliation><mods:affiliation>Laboratory of Comparative Neurobiology, Scripps Institution of Oceanography and Department of Neurosciences, School of Medicine, University of California, San Diego, La Jolla, California 92037</mods:affiliation></affiliation></author><author><name sortKey="Gonzalez, Agustin" sort="Gonzalez, Agustin" uniqKey="Gonzalez A" first="Agustín" last="González">Agustín González</name><affiliation><mods:affiliation>Department of Cell Biology, Faculty of Biology, University Complutense, 28040 Madrid, Spain</mods:affiliation></affiliation><affiliation><mods:affiliation>Departamento de Biología Celular, Facultad de Biología, Universidad Complutense, 28040 Madrid, Spain</mods:affiliation></affiliation></author></titleStmt><publicationStmt><idno type="wicri:source">ISTEX</idno><idno type="RBID">ISTEX:BDE0A19858D8C1F1E4C1040C46A237D8E2184F97</idno><date when="2013" year="2013">2013</date><idno type="doi">10.1002/cne.23155</idno><idno type="url">https://api.istex.fr/document/BDE0A19858D8C1F1E4C1040C46A237D8E2184F97/fulltext/pdf</idno><idno type="wicri:Area/Istex/Corpus">001535</idno><idno type="wicri:explorRef" wicri:stream="Istex" wicri:step="Corpus" wicri:corpus="ISTEX">001535</idno></publicationStmt><sourceDesc><biblStruct><analytic><title level="a" type="main" xml:lang="en">Neuroanatomical organization of the cholinergic system in the central nervous system of a basal actinopterygian fish, the senegal bichir Polypterus senegalus</title><author><name sortKey="L Pez, Jesus M" sort="L Pez, Jesus M" uniqKey="L Pez J" first="Jesús M." last="L Pez">Jesús M. L Pez</name><affiliation><mods:affiliation>Department of Cell Biology, Faculty of Biology, University Complutense, 28040 Madrid, Spain</mods:affiliation></affiliation></author><author><name sortKey="Perlado, Jorge" sort="Perlado, Jorge" uniqKey="Perlado J" first="Jorge" last="Perlado">Jorge Perlado</name><affiliation><mods:affiliation>Department of Cell Biology, Faculty of Biology, University Complutense, 28040 Madrid, Spain</mods:affiliation></affiliation></author><author><name sortKey="Morona, Ruth" sort="Morona, Ruth" uniqKey="Morona R" first="Ruth" last="Morona">Ruth Morona</name><affiliation><mods:affiliation>Department of Cell Biology, Faculty of Biology, University Complutense, 28040 Madrid, Spain</mods:affiliation></affiliation></author><author><name sortKey="Northcutt, R Glenn" sort="Northcutt, R Glenn" uniqKey="Northcutt R" first="R. Glenn" last="Northcutt">R. Glenn Northcutt</name><affiliation><mods:affiliation>Laboratory of Comparative Neurobiology, Scripps Institution of Oceanography and Department of Neurosciences, School of Medicine, University of California, San Diego, La Jolla, California 92037</mods:affiliation></affiliation></author><author><name sortKey="Gonzalez, Agustin" sort="Gonzalez, Agustin" uniqKey="Gonzalez A" first="Agustín" last="González">Agustín González</name><affiliation><mods:affiliation>Department of Cell Biology, Faculty of Biology, University Complutense, 28040 Madrid, Spain</mods:affiliation></affiliation><affiliation><mods:affiliation>Departamento de Biología Celular, Facultad de Biología, Universidad Complutense, 28040 Madrid, Spain</mods:affiliation></affiliation></author></analytic><monogr></monogr><series><title level="j">Journal of Comparative Neurology</title><title level="j" type="abbrev">J. Comp. 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The cholinergic system has been characterized in more advanced ray‐finned fishes, but not in polypterids. In order to establish which cholinergic neural centers characterized the earliest ray‐finned fishes, the distribution of choline acetyltransferase (ChAT) is described in Polypterus and compared with the distribution of this molecule in other ray‐finned fishes. Cell groups immunoreactive for ChAT were observed in the hypothalamus, the habenula, the optic tectum, the isthmus, the cranial motor nuclei, and the spinal motor column. Cholinergic fibers were observed in both the telencephalic pallium and the subpallium, in the thalamus and pretectum, in the optic tectum and torus semicircularis, in the mesencephalic tegmentum, in the cerebellar crest, in the solitary nucleus, and in the dorsal column nuclei. Comparison of the data within a segmental neuromeric context indicates that the cholinergic system in polypterid fishes is generally similar to that in other ray‐finned fishes, but cholinergic‐positive neurons in the pallium and subpallium, and in the thalamus and cerebellum, of teleosts appear to have evolved following the separation of polypterids and other ray‐finned fishes. J. Comp. Neurol. 521:24–49, 2013. © 2012 Wiley Periodicals, Inc.</div></front></TEI><istex><corpusName>wiley</corpusName><author><json:item><name>Jesús M. 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The cholinergic system has been characterized in more advanced ray‐finned fishes, but not in polypterids. In order to establish which cholinergic neural centers characterized the earliest ray‐finned fishes, the distribution of choline acetyltransferase (ChAT) is described in Polypterus and compared with the distribution of this molecule in other ray‐finned fishes. Cell groups immunoreactive for ChAT were observed in the hypothalamus, the habenula, the optic tectum, the isthmus, the cranial motor nuclei, and the spinal motor column. Cholinergic fibers were observed in both the telencephalic pallium and the subpallium, in the thalamus and pretectum, in the optic tectum and torus semicircularis, in the mesencephalic tegmentum, in the cerebellar crest, in the solitary nucleus, and in the dorsal column nuclei. Comparison of the data within a segmental neuromeric context indicates that the cholinergic system in polypterid fishes is generally similar to that in other ray‐finned fishes, but cholinergic‐positive neurons in the pallium and subpallium, and in the thalamus and cerebellum, of teleosts appear to have evolved following the separation of polypterids and other ray‐finned fishes. J. Comp. 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Neurol.</title><idno type="pISSN">0021-9967</idno><idno type="eISSN">1096-9861</idno><idno type="DOI">10.1002/(ISSN)1096-9861</idno><imprint><publisher>Wiley Subscription Services, Inc., A Wiley Company</publisher><pubPlace>Hoboken</pubPlace><date type="published" when="2013-01-01"></date><biblScope unit="volume">521</biblScope><biblScope unit="issue">1</biblScope><biblScope unit="page" from="24">24</biblScope><biblScope unit="page" to="49">49</biblScope></imprint></monogr><idno type="istex">BDE0A19858D8C1F1E4C1040C46A237D8E2184F97</idno><idno type="DOI">10.1002/cne.23155</idno><idno type="ArticleID">CNE23155</idno></biblStruct></sourceDesc></fileDesc><profileDesc><creation><date>2013</date></creation><langUsage><language ident="en">en</language></langUsage><abstract xml:lang="en"><p>Polypterid bony fishes are believed to be basal to other living ray‐finned fishes, and their brain organization is therefore critical in providing information as to primitive neural characters that existed in the earliest ray‐finned fishes. The cholinergic system has been characterized in more advanced ray‐finned fishes, but not in polypterids. In order to establish which cholinergic neural centers characterized the earliest ray‐finned fishes, the distribution of choline acetyltransferase (ChAT) is described in Polypterus and compared with the distribution of this molecule in other ray‐finned fishes. Cell groups immunoreactive for ChAT were observed in the hypothalamus, the habenula, the optic tectum, the isthmus, the cranial motor nuclei, and the spinal motor column. Cholinergic fibers were observed in both the telencephalic pallium and the subpallium, in the thalamus and pretectum, in the optic tectum and torus semicircularis, in the mesencephalic tegmentum, in the cerebellar crest, in the solitary nucleus, and in the dorsal column nuclei. Comparison of the data within a segmental neuromeric context indicates that the cholinergic system in polypterid fishes is generally similar to that in other ray‐finned fishes, but cholinergic‐positive neurons in the pallium and subpallium, and in the thalamus and cerebellum, of teleosts appear to have evolved following the separation of polypterids and other ray‐finned fishes. J. Comp. Neurol. 521:24–49, 2013. © 2012 Wiley Periodicals, Inc.</p></abstract><abstract xml:lang="en" style="graphical"><p></p></abstract><textClass xml:lang="en"><keywords scheme="keyword"><list><head>keywords</head><item><term>acetylcholine</term></item><item><term>immunohistochemistry</term></item><item><term>segmental organization</term></item><item><term>cladistians</term></item><item><term>brain evolution</term></item><item><term>motor nuclei</term></item><item><term>nucleus medianus magnocellularis</term></item></list></keywords></textClass><textClass><keywords scheme="Journal Subject"><list><head>article-category</head><item><term>Research Article</term></item></list></keywords></textClass></profileDesc><revisionDesc><change when="2012-04-17">Received</change><change when="2012-05-18">Registration</change><change when="2013-01-01">Published</change></revisionDesc></teiHeader></istex:fulltextTEI><json:item><extension>txt</extension><original>false</original><mimetype>text/plain</mimetype><uri>https://api.istex.fr/document/BDE0A19858D8C1F1E4C1040C46A237D8E2184F97/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>Wiley Subscription Services, Inc., A Wiley Company</publisherName><publisherLoc>Hoboken</publisherLoc></publisherInfo><doi registered="yes">10.1002/(ISSN)1096-9861</doi><issn type="print">0021-9967</issn><issn type="electronic">1096-9861</issn><idGroup><id type="product" value="CNE"></id></idGroup><titleGroup><title type="main" xml:lang="en" sort="JOURNAL OF COMPARATIVE NEUROLOGY">Journal of Comparative Neurology</title><title type="short">J. 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Glenn</givenNames><familyName>Northcutt</familyName></personName></creator><creator xml:id="au5" creatorRole="author" affiliationRef="#af1" corresponding="yes"><personName><givenNames>Agustín</givenNames><familyName>González</familyName></personName><contactDetails><email>agustin@bio.ucm.es</email></contactDetails></creator></creators><affiliationGroup><affiliation xml:id="af1" countryCode="ES" type="organization"><unparsedAffiliation>Department of Cell Biology, Faculty of Biology, University Complutense, 28040 Madrid, Spain</unparsedAffiliation></affiliation><affiliation xml:id="af2" countryCode="US" type="organization"><unparsedAffiliation>Laboratory of Comparative Neurobiology, Scripps Institution of Oceanography and Department of Neurosciences, School of Medicine, University of California, San Diego, La Jolla, California 92037</unparsedAffiliation></affiliation></affiliationGroup><keywordGroup xml:lang="en" type="author"><keyword xml:id="kwd1">acetylcholine</keyword><keyword xml:id="kwd2">immunohistochemistry</keyword><keyword xml:id="kwd3">segmental organization</keyword><keyword xml:id="kwd4">cladistians</keyword><keyword xml:id="kwd5">brain evolution</keyword><keyword xml:id="kwd6">motor nuclei</keyword><keyword xml:id="kwd7">nucleus medianus magnocellularis</keyword></keywordGroup><fundingInfo><fundingAgency>the Spanish Ministry of Science and Technology</fundingAgency><fundingNumber>BFU2009‐12315</fundingNumber><fundingNumber>BFU2012‐31687</fundingNumber></fundingInfo><fundingInfo><fundingAgency>the U.S. National Science Foundation</fundingAgency><fundingNumber>1120844</fundingNumber></fundingInfo><supportingInformation><p> Additional Supporting Information may be found in the online version of this article. </p><supportingInfoItem><mediaResource alt="supporting information" href="urn-x:wiley:00219967:media:cne23155:CNE_23155_sm_SuppFig1"></mediaResource><caption>Supporting Figure 1: (Magenta‐green version for the assistance of color blind readers.) Photomicrographs of transverse (a, b, d, f‐h) and sagittal (c, e) sections through the brain of Polypterus, illustrating staining in the same sections for ChAT (red fluorescence) and either TH (a‐e, h) or Islet1 (f‐h) (green fluorescence). The relationship between the distinct cell populations is illustrated for: (a) the rostral part of the supraoptoparaventricular band; (b) the magnocellular part of the supraoptoparaventricular band and the suprachiasmatic nucleus; (c) the oculomotor and trochlear nuclei and the pretectum; (d) transverse section through the pretectal region at the level indicated in c (arrow points to the fibers ascending toward the pretectal neuropil); (e) the trigeminal motor nucleus just caudal to the THir cells of the locus coeruleus; (f) transverse section through the motor nucleus of the trigeminus and the ventral nucleus of the octavolateral area (note nuclear Isl1staining in motor cells); (g) the nucleus medianus magnocellularis, the vagal motor nucleus, and the rostral cells of the spino‐occipital nucleus (all double labeled); (h) the retina with distinct ChATir and THir cells. Scale bars = 200 μm (b‐e), 100 μm (a, f, g), 50 μm (h).</caption></supportingInfoItem></supportingInformation><abstractGroup><abstract type="main" xml:lang="en"><title type="main">Abstract</title><p>Polypterid bony fishes are believed to be basal to other living ray‐finned fishes, and their brain organization is therefore critical in providing information as to primitive neural characters that existed in the earliest ray‐finned fishes. The cholinergic system has been characterized in more advanced ray‐finned fishes, but not in polypterids. In order to establish which cholinergic neural centers characterized the earliest ray‐finned fishes, the distribution of choline acetyltransferase (ChAT) is described in <i>Polypterus</i> and compared with the distribution of this molecule in other ray‐finned fishes. Cell groups immunoreactive for ChAT were observed in the hypothalamus, the habenula, the optic tectum, the isthmus, the cranial motor nuclei, and the spinal motor column. Cholinergic fibers were observed in both the telencephalic pallium and the subpallium, in the thalamus and pretectum, in the optic tectum and torus semicircularis, in the mesencephalic tegmentum, in the cerebellar crest, in the solitary nucleus, and in the dorsal column nuclei. Comparison of the data within a segmental neuromeric context indicates that the cholinergic system in polypterid fishes is generally similar to that in other ray‐finned fishes, but cholinergic‐positive neurons in the pallium and subpallium, and in the thalamus and cerebellum, of teleosts appear to have evolved following the separation of polypterids and other ray‐finned fishes. J. Comp. Neurol. 521:24–49, 2013. © 2012 Wiley Periodicals, Inc.</p></abstract><abstract type="graphical" xml:lang="en"><p><blockFixed type="graphic"><mediaResourceGroup><mediaResource alt="image" copyright="Wiley Periodicals, Inc." href="urn:x-wiley:00219967:media:CNE23155:gra001"></mediaResource></mediaResourceGroup></blockFixed></p></abstract></abstractGroup></contentMeta></header></component></istex:document></istex:metadataXml><mods version="3.6"><titleInfo lang="en"><title>Neuroanatomical organization of the cholinergic system in the central nervous system of a basal actinopterygian fish, the senegal bichir Polypterus senegalus</title></titleInfo><titleInfo type="abbreviated" lang="en"><title>Cholinergic System of polypterus</title></titleInfo><titleInfo type="alternative" contentType="CDATA" lang="en"><title>Neuroanatomical organization of the cholinergic system in the central nervous system of a basal actinopterygian fish, the senegal bichir Polypterus senegalus</title></titleInfo><name type="personal"><namePart type="given">Jesús M.</namePart><namePart type="family">López</namePart><affiliation>Department of Cell Biology, Faculty of Biology, University Complutense, 28040 Madrid, Spain</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Jorge</namePart><namePart type="family">Perlado</namePart><affiliation>Department of Cell Biology, Faculty of Biology, University Complutense, 28040 Madrid, Spain</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Ruth</namePart><namePart type="family">Morona</namePart><affiliation>Department of Cell Biology, Faculty of Biology, University Complutense, 28040 Madrid, Spain</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">R. Glenn</namePart><namePart type="family">Northcutt</namePart><affiliation>Laboratory of Comparative Neurobiology, Scripps Institution of Oceanography and Department of Neurosciences, School of Medicine, University of California, San Diego, La Jolla, California 92037</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Agustín</namePart><namePart type="family">González</namePart><affiliation>Department of Cell Biology, Faculty of Biology, University Complutense, 28040 Madrid, Spain</affiliation><affiliation>Departamento de Biología Celular, Facultad de Biología, Universidad Complutense, 28040 Madrid, Spain</affiliation><role><roleTerm type="text">author</roleTerm></role></name><typeOfResource>text</typeOfResource><genre type="article" displayLabel="article"></genre><originInfo><publisher>Wiley Subscription Services, Inc., A Wiley Company</publisher><place><placeTerm type="text">Hoboken</placeTerm></place><dateIssued encoding="w3cdtf">2013-01-01</dateIssued><dateCaptured encoding="w3cdtf">2012-04-17</dateCaptured><dateValid encoding="w3cdtf">2012-05-18</dateValid><copyrightDate encoding="w3cdtf">2013</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">7</extent><extent unit="tables">3</extent><extent unit="references">184</extent><extent unit="words">20395</extent></physicalDescription><abstract lang="en">Polypterid bony fishes are believed to be basal to other living ray‐finned fishes, and their brain organization is therefore critical in providing information as to primitive neural characters that existed in the earliest ray‐finned fishes. The cholinergic system has been characterized in more advanced ray‐finned fishes, but not in polypterids. In order to establish which cholinergic neural centers characterized the earliest ray‐finned fishes, the distribution of choline acetyltransferase (ChAT) is described in Polypterus and compared with the distribution of this molecule in other ray‐finned fishes. Cell groups immunoreactive for ChAT were observed in the hypothalamus, the habenula, the optic tectum, the isthmus, the cranial motor nuclei, and the spinal motor column. Cholinergic fibers were observed in both the telencephalic pallium and the subpallium, in the thalamus and pretectum, in the optic tectum and torus semicircularis, in the mesencephalic tegmentum, in the cerebellar crest, in the solitary nucleus, and in the dorsal column nuclei. Comparison of the data within a segmental neuromeric context indicates that the cholinergic system in polypterid fishes is generally similar to that in other ray‐finned fishes, but cholinergic‐positive neurons in the pallium and subpallium, and in the thalamus and cerebellum, of teleosts appear to have evolved following the separation of polypterids and other ray‐finned fishes. J. Comp. Neurol. 521:24–49, 2013. © 2012 Wiley Periodicals, Inc.</abstract><abstract type="graphical" lang="en"></abstract><note type="funding">the Spanish Ministry of Science and Technology - No. BFU2009‐12315; No. BFU2012‐31687; </note><note type="funding">the U.S. National Science Foundation - No. 1120844; </note><subject lang="en"><genre>keywords</genre><topic>acetylcholine</topic><topic>immunohistochemistry</topic><topic>segmental organization</topic><topic>cladistians</topic><topic>brain evolution</topic><topic>motor nuclei</topic><topic>nucleus medianus magnocellularis</topic></subject><relatedItem type="host"><titleInfo><title>Journal of Comparative Neurology</title></titleInfo><titleInfo type="abbreviated"><title>J. Comp. Neurol.</title></titleInfo><genre type="journal">journal</genre><note type="content"> Additional Supporting Information may be found in the online version of this article.Supporting Info Item: Supporting Figure 1: (Magenta‐green version for the assistance of color blind readers.) Photomicrographs of transverse (a, b, d, f‐h) and sagittal (c, e) sections through the brain of Polypterus, illustrating staining in the same sections for ChAT (red fluorescence) and either TH (a‐e, h) or Islet1 (f‐h) (green fluorescence). The relationship between the distinct cell populations is illustrated for: (a) the rostral part of the supraoptoparaventricular band; (b) the magnocellular part of the supraoptoparaventricular band and the suprachiasmatic nucleus; (c) the oculomotor and trochlear nuclei and the pretectum; (d) transverse section through the pretectal region at the level indicated in c (arrow points to the fibers ascending toward the pretectal neuropil); (e) the trigeminal motor nucleus just caudal to the THir cells of the locus coeruleus; (f) transverse section through the motor nucleus of the trigeminus and the ventral nucleus of the octavolateral area (note nuclear Isl1staining in motor cells); (g) the nucleus medianus magnocellularis, the vagal motor nucleus, and the rostral cells of the spino‐occipital nucleus (all double labeled); (h) the retina with distinct ChATir and THir cells. Scale bars = 200 μm (b‐e), 100 μm (a, f, g), 50 μm (h). - </note><subject><genre>article-category</genre><topic>Research Article</topic></subject><identifier type="ISSN">0021-9967</identifier><identifier type="eISSN">1096-9861</identifier><identifier type="DOI">10.1002/(ISSN)1096-9861</identifier><identifier type="PublisherID">CNE</identifier><part><date>2013</date><detail type="volume"><caption>vol.</caption><number>521</number></detail><detail type="issue"><caption>no.</caption><number>1</number></detail><extent unit="pages"><start>24</start><end>49</end><total>27</total></extent></part></relatedItem><identifier type="istex">BDE0A19858D8C1F1E4C1040C46A237D8E2184F97</identifier><identifier type="DOI">10.1002/cne.23155</identifier><identifier type="ArticleID">CNE23155</identifier><accessCondition type="use and reproduction" contentType="copyright">Copyright © 2012 Wiley Periodicals, Inc.</accessCondition><recordInfo><recordContentSource>WILEY</recordContentSource><recordOrigin>Wiley Subscription Services, Inc., A Wiley Company</recordOrigin></recordInfo></mods></metadata><serie></serie></istex></record>Pour manipuler ce document sous Unix (Dilib)
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