A Comparison Between Thrombocytes and Monocyte‐Macrophages in Salmo gairdneri Richardson: A Cytoenzymatic Evaluation
Identifieur interne : 001622 ( Istex/Corpus ); précédent : 001621; suivant : 001623A Comparison Between Thrombocytes and Monocyte‐Macrophages in Salmo gairdneri Richardson: A Cytoenzymatic Evaluation
Auteurs : M. R. Ribaud ; L. Passantino ; A. Perillo ; F. Jirillo ; M. Carrassi ; E. Jirillo ; G. F. PassantinoSource :
- Anatomia, Histologia, Embryologia [ 0340-2096 ] ; 2005-12.
Abstract
Fish leukocyte heterogenity with respect to morphology, morphometry and immunological function has been object of some controversy, mostly because, in lower vertebrates, there are several interspecies differences. Leukocyte enzyme cytochemistry permits cellular differentiation, which is otherwise not possible with routine stains, and may also indicate cell function. In fish, phagocytic performance is principally operated by monocyte‐macrophages (MØ) present in tissues and in circulating blood. Fish thrombocytes (FTHR), even if they are the equivalent of platelets in mammals, are complete cells with cytoplasm and nucleus. They vary in shape from round, like small lymphocytes, to spindle‐shaped or rod‐shaped cells. Several cytochemical methods, as periodic acid Schiff (PAS), naphthol chloroacetate esterase (ASD), α‐naphthyl acetate esterase (ANAE), peroxidase (PEROX), acid phosphatase (Ac. Phos.) with and without tartaric acid (ta) and alkaline phosphatase (Alk. Phos.) have been applied in Salmo gairdneri Richardson to investigate the expression of MØ and FTHR enzyme patterns. Here, we compared cytochemistry between fish MØ and FTHR, and between human MØ and platelets/megakaryocytes, respectively, as indicated in the table. It appears that positivity to some enzyme cytochemistry is phylogenetically maintained in MØ, while in FTHR the enzyme pattern has undergone modification during evolution. For instance, this is the case of ANAE, Ac. Phos. and Alk. Phos., which changed in the phylogenesis, while PAS, AS‐D, PEROX are still present in the evolution. PAS AS‐D ANAE Perox Ac.Phos.‐ta Ac.Phos.+ta Alk. Phos Trout MØ ++ + ++ ++ + − n.d. Human MØ + + ++ + − − − Trout THR −/++ − − − −/+ − ++ Human platelets/ megakaryocytes + − ++ − + + − +, Positive; ++, strongly positive; (, negative; n.d., not determined.
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DOI: 10.1111/j.1439-0264.2005.00669_96.x
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Leukocyte enzyme cytochemistry permits cellular differentiation, which is otherwise not possible with routine stains, and may also indicate cell function. In fish, phagocytic performance is principally operated by monocyte‐macrophages (MØ) present in tissues and in circulating blood. Fish thrombocytes (FTHR), even if they are the equivalent of platelets in mammals, are complete cells with cytoplasm and nucleus. They vary in shape from round, like small lymphocytes, to spindle‐shaped or rod‐shaped cells. Several cytochemical methods, as periodic acid Schiff (PAS), naphthol chloroacetate esterase (ASD), α‐naphthyl acetate esterase (ANAE), peroxidase (PEROX), acid phosphatase (Ac. Phos.) with and without tartaric acid (ta) and alkaline phosphatase (Alk. Phos.) have been applied in Salmo gairdneri Richardson to investigate the expression of MØ and FTHR enzyme patterns. Here, we compared cytochemistry between fish MØ and FTHR, and between human MØ and platelets/megakaryocytes, respectively, as indicated in the table. It appears that positivity to some enzyme cytochemistry is phylogenetically maintained in MØ, while in FTHR the enzyme pattern has undergone modification during evolution. For instance, this is the case of ANAE, Ac. Phos. and Alk. Phos., which changed in the phylogenesis, while PAS, AS‐D, PEROX are still present in the evolution. PAS AS‐D ANAE Perox Ac.Phos.‐ta Ac.Phos.+ta Alk. Phos Trout MØ ++ + ++ ++ + − n.d. Human MØ + + ++ + − − − Trout THR −/++ − − − −/+ − ++ Human platelets/ megakaryocytes + − ++ − + + − +, Positive; ++, strongly positive; (, negative; n.d., not determined.</div></front></TEI><istex><corpusName>wiley</corpusName><author><json:item><name>M. R. Ribaud</name><affiliations><json:string>Department of Animal Health and Welfare, Faculty of Veterinary Medicine, University of Bari, Str. 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Prov. le per Casamassima Km 3, 70010, Valenzano (BA)</json:string></affiliations></json:item></author><articleId><json:string>AHE669_96_96</json:string></articleId><language><json:string>eng</json:string></language><originalGenre><json:string>abstract</json:string></originalGenre><abstract>Fish leukocyte heterogenity with respect to morphology, morphometry and immunological function has been object of some controversy, mostly because, in lower vertebrates, there are several interspecies differences. Leukocyte enzyme cytochemistry permits cellular differentiation, which is otherwise not possible with routine stains, and may also indicate cell function. In fish, phagocytic performance is principally operated by monocyte‐macrophages (MØ) present in tissues and in circulating blood. Fish thrombocytes (FTHR), even if they are the equivalent of platelets in mammals, are complete cells with cytoplasm and nucleus. They vary in shape from round, like small lymphocytes, to spindle‐shaped or rod‐shaped cells. Several cytochemical methods, as periodic acid Schiff (PAS), naphthol chloroacetate esterase (ASD), α‐naphthyl acetate esterase (ANAE), peroxidase (PEROX), acid phosphatase (Ac. Phos.) with and without tartaric acid (ta) and alkaline phosphatase (Alk. Phos.) have been applied in Salmo gairdneri Richardson to investigate the expression of MØ and FTHR enzyme patterns. Here, we compared cytochemistry between fish MØ and FTHR, and between human MØ and platelets/megakaryocytes, respectively, as indicated in the table. It appears that positivity to some enzyme cytochemistry is phylogenetically maintained in MØ, while in FTHR the enzyme pattern has undergone modification during evolution. For instance, this is the case of ANAE, Ac. Phos. and Alk. Phos., which changed in the phylogenesis, while PAS, AS‐D, PEROX are still present in the evolution. PAS AS‐D ANAE Perox Ac.Phos.‐ta Ac.Phos.+ta Alk. Phos Trout MØ ++ + ++ ++ + − n.d. 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R.</forename><surname>Ribaud</surname></persName><affiliation>Department of Animal Health and Welfare, Faculty of Veterinary Medicine, University of Bari, Str. Prov. le per Casamassima Km 3, 70010, Valenzano (BA)</affiliation></author><author xml:id="author-2"><persName><forename type="first">L.</forename><surname>Passantino</surname></persName><affiliation>Department of Animal Health and Welfare, Faculty of Veterinary Medicine, University of Bari, Str. Prov. le per Casamassima Km 3, 70010, Valenzano (BA)</affiliation></author><author xml:id="author-3"><persName><forename type="first">A.</forename><surname>Perillo</surname></persName><affiliation>Department of Animal Health and Welfare, Faculty of Veterinary Medicine, University of Bari, Str. Prov. le per Casamassima Km 3, 70010, Valenzano (BA)</affiliation></author><author xml:id="author-4"><persName><forename type="first">F.</forename><surname>Jirillo</surname></persName><affiliation>Department of Internal Medicine, Immunology and Infectious Disease, Section of Microbiology and Immunology, Faculty of Medicine, University of Bari, Policlinico ‐Piazza G. Cesare‐ 70124 – Bari, Italy</affiliation></author><author xml:id="author-5"><persName><forename type="first">M.</forename><surname>Carrassi</surname></persName><affiliation>Department of Animal Health and Welfare, Faculty of Veterinary Medicine, University of Bari, Str. Prov. le per Casamassima Km 3, 70010, Valenzano (BA)</affiliation></author><author xml:id="author-6"><persName><forename type="first">E.</forename><surname>Jirillo</surname></persName><affiliation>Department of Animal Health and Welfare, Faculty of Veterinary Medicine, University of Bari, Str. 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Leukocyte enzyme cytochemistry permits cellular differentiation, which is otherwise not possible with routine stains, and may also indicate cell function. In fish, phagocytic performance is principally operated by monocyte‐macrophages (MØ) present in tissues and in circulating blood. Fish thrombocytes (FTHR), even if they are the equivalent of platelets in mammals, are complete cells with cytoplasm and nucleus. They vary in shape from round, like small lymphocytes, to spindle‐shaped or rod‐shaped cells. Several cytochemical methods, as periodic acid Schiff (PAS), naphthol chloroacetate esterase (ASD), α‐naphthyl acetate esterase (ANAE), peroxidase (PEROX), acid phosphatase (Ac. Phos.) with and without tartaric acid (ta) and alkaline phosphatase (Alk. Phos.) have been applied in Salmo gairdneri Richardson to investigate the expression of MØ and FTHR enzyme patterns. Here, we compared cytochemistry between fish MØ and FTHR, and between human MØ and platelets/megakaryocytes, respectively, as indicated in the table. It appears that positivity to some enzyme cytochemistry is phylogenetically maintained in MØ, while in FTHR the enzyme pattern has undergone modification during evolution. For instance, this is the case of ANAE, Ac. Phos. and Alk. Phos., which changed in the phylogenesis, while PAS, AS‐D, PEROX are still present in the evolution. PAS AS‐D ANAE Perox Ac.Phos.‐ta Ac.Phos.+ta Alk. Phos Trout MØ ++ + ++ ++ + − n.d. Human MØ + + ++ + − − − Trout THR −/++ − − − −/+ − ++ Human platelets/ megakaryocytes + − ++ − + + − +, Positive; ++, strongly positive; (, negative; n.d., not determined.</p></abstract></profileDesc><revisionDesc><change when="2005-12">Published</change><change xml:id="refBibs-istex" who="#ISTEX-API" when="2016-12-13">References added</change><change xml:id="refBibs-istex" who="#ISTEX-API" when="2017-02-9">References added</change></revisionDesc></teiHeader></istex:fulltextTEI><json:item><extension>txt</extension><original>false</original><mimetype>text/plain</mimetype><uri>https://api.istex.fr/document/919052E1E7FC92C14503EFE7A060F2EF8A9CD7AE/fulltext/txt</uri></json:item></fulltext><metadata><istex:metadataXml wicri:clean="Wiley component found"><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 Verlag GmbH</publisherName><publisherLoc>Berlin, Germany</publisherLoc></publisherInfo><doi origin="wiley" registered="yes">10.1111/(ISSN)1439-0264</doi><issn type="print">0340-2096</issn><issn type="electronic">1439-0264</issn><idGroup><id type="product" value="AHE"></id><id type="publisherDivision" value="ST"></id></idGroup><titleGroup><title type="main" sort="ANATOMIA HISTOLOGIA EMBRYOLOGIA">Anatomia, Histologia, Embryologia</title></titleGroup></publicationMeta><publicationMeta level="part" position="12000"><doi origin="wiley">10.1111/ahe.2005.34.issue-s1</doi><numberingGroup><numbering type="journalVolume" number="34">34</numbering><numbering type="supplement">s1</numbering></numberingGroup><coverDate startDate="2005-12">December 2005</coverDate></publicationMeta><publicationMeta level="unit" type="abstract" position="1" status="forIssue"><doi origin="wiley">10.1111/j.1439-0264.2005.00669_96.x</doi><idGroup><id type="unit" value="AHE669_96_96"></id></idGroup><titleGroup><title type="tocHeading1">Abstracts of the XXVth Congress of the European Association of Veterinary Anatomists (EAVA), Oslo, 28–31 July 2004</title></titleGroup><eventGroup><event type="firstOnline" date="2005-11-22"></event><event type="publishedOnlineFinalForm" date="2005-11-22"></event><event type="xmlConverted" agent="Converter:BPG_TO_WML3G version:2.3.6 mode:FullText source:Header result:Header" date="2010-04-14"></event><event type="xmlConverted" agent="Converter:WILEY_ML3G_TO_WILEY_ML3GV2 version:3.8.8" date="2014-01-01"></event><event type="xmlConverted" agent="Converter:WML3G_To_WML3G version:4.1.7 mode:FullText,remove_FC" date="2014-10-14"></event></eventGroup><numberingGroup><numbering type="pageFirst" number="42">42</numbering><numbering type="pageLast" number="43">43</numbering></numberingGroup><linkGroup><link type="toTypesetVersion" href="file:AHE.AHE669_96_96.pdf"></link></linkGroup></publicationMeta><contentMeta><titleGroup><title type="main">A Comparison Between Thrombocytes and Monocyte‐Macrophages in Salmo gairdneri Richardson: A Cytoenzymatic Evaluation</title><title type="short">Abstracts</title></titleGroup><creators><creator creatorRole="author" xml:id="cr1" affiliationRef="#a96-1"><personName><givenNames>M. R.</givenNames><familyName>Ribaud</familyName></personName></creator><creator creatorRole="author" xml:id="cr2" affiliationRef="#a96-1"><personName><givenNames>L.</givenNames><familyName>Passantino</familyName></personName></creator><creator creatorRole="author" xml:id="cr3" affiliationRef="#a96-1"><personName><givenNames>A.</givenNames><familyName>Perillo</familyName></personName></creator><creator creatorRole="author" xml:id="cr4" affiliationRef="#a96-2"><personName><givenNames>F.</givenNames><familyName>Jirillo</familyName></personName></creator><creator creatorRole="author" xml:id="cr5" affiliationRef="#a96-1"><personName><givenNames>M.</givenNames><familyName>Carrassi</familyName></personName></creator><creator creatorRole="author" xml:id="cr6" affiliationRef="#a96-1"><personName><givenNames>E.</givenNames><familyName>Jirillo</familyName></personName></creator><creator creatorRole="author" xml:id="cr7" affiliationRef="#a96-1"><personName><givenNames>G. F.</givenNames><familyName>Passantino</familyName></personName></creator></creators><affiliationGroup><affiliation xml:id="a96-1"><unparsedAffiliation>Department of Animal Health and Welfare, Faculty of Veterinary Medicine, University of Bari, Str. Prov. le per Casamassima Km 3, 70010, Valenzano (BA)</unparsedAffiliation></affiliation><affiliation xml:id="a96-2" countryCode="IT"><unparsedAffiliation>Department of Internal Medicine, Immunology and Infectious Disease, Section of Microbiology and Immunology, Faculty of Medicine, University of Bari, Policlinico ‐Piazza G. Cesare‐ 70124 – Bari, Italy</unparsedAffiliation></affiliation></affiliationGroup><abstractGroup><abstract type="main" xml:lang="en"><p>Fish leukocyte heterogenity with respect to morphology, morphometry and immunological function has been object of some controversy, mostly because, in lower vertebrates, there are several interspecies differences. Leukocyte enzyme cytochemistry permits cellular differentiation, which is otherwise not possible with routine stains, and may also indicate cell function. In fish, phagocytic performance is principally operated by monocyte‐macrophages (MØ) present in tissues and in circulating blood. Fish thrombocytes (FTHR), even if they are the equivalent of platelets in mammals, are complete cells with cytoplasm and nucleus. They vary in shape from round, like small lymphocytes, to spindle‐shaped or rod‐shaped cells. Several cytochemical methods, as periodic acid Schiff (PAS), naphthol chloroacetate esterase (ASD), α‐naphthyl acetate esterase (ANAE), peroxidase (PEROX), acid phosphatase (Ac. Phos.) with and without tartaric acid (ta) and alkaline phosphatase (Alk. Phos.) have been applied in Salmo gairdneri Richardson to investigate the expression of MØ and FTHR enzyme patterns. Here, we compared cytochemistry between fish MØ and FTHR, and between human MØ and platelets/megakaryocytes, respectively, as indicated in the table. It appears that positivity to some enzyme cytochemistry is phylogenetically maintained in MØ, while in FTHR the enzyme pattern has undergone modification during evolution. For instance, this is the case of ANAE, Ac. Phos. and Alk. Phos., which changed in the phylogenesis, while PAS, AS‐D, PEROX are still present in the evolution.</p><p> <tabularFixed><table frame="topbot"><tgroup cols="8" align="left"><colspec colnum="1" colname="col1"></colspec><colspec colnum="2" colname="col2"></colspec><colspec colnum="3" colname="col3"></colspec><colspec colnum="4" colname="col4"></colspec><colspec colnum="5" colname="col5"></colspec><colspec colnum="6" colname="col6"></colspec><colspec colnum="7" colname="col7"></colspec><colspec colnum="8" colname="col8"></colspec><thead valign="bottom"><row rowsep="1"><entry></entry><entry>PAS</entry><entry>AS‐D</entry><entry>ANAE</entry><entry>Perox</entry><entry>Ac.Phos.‐ta</entry><entry>Ac.Phos.+ta</entry><entry>Alk. Phos</entry></row></thead><tbody valign="top"><row><entry>Trout MØ</entry><entry>++</entry><entry>+</entry><entry>++</entry><entry>++</entry><entry>+</entry><entry>−</entry><entry>n.d.</entry></row><row><entry>Human MØ</entry><entry>+</entry><entry>+</entry><entry>++</entry><entry>+</entry><entry>−</entry><entry>−</entry><entry>−</entry></row><row><entry>Trout THR</entry><entry>−/++</entry><entry>−</entry><entry>−</entry><entry>−</entry><entry>−/+</entry><entry>−</entry><entry>++</entry></row><row><entry>Human platelets/ megakaryocytes</entry><entry>+</entry><entry>−</entry><entry>++</entry><entry>−</entry><entry>+</entry><entry>+</entry><entry>−</entry></row></tbody></tgroup></table><noteGroup><note xml:id="tu1_note40" numbered="no"><p>+, Positive; ++, strongly positive; (, negative; n.d., not determined.</p></note></noteGroup></tabularFixed> </p></abstract></abstractGroup></contentMeta></header></component></istex:document></istex:metadataXml><mods version="3.6"><titleInfo lang="en"><title>A Comparison Between Thrombocytes and Monocyte‐Macrophages in Salmo gairdneri Richardson: A Cytoenzymatic Evaluation</title></titleInfo><titleInfo type="abbreviated" lang="en"><title>Abstracts</title></titleInfo><titleInfo type="alternative" contentType="CDATA" lang="en"><title>A Comparison Between Thrombocytes and Monocyte‐Macrophages in Salmo gairdneri Richardson: A Cytoenzymatic Evaluation</title></titleInfo><name type="personal"><namePart type="given">M. R.</namePart><namePart type="family">Ribaud</namePart><affiliation>Department of Animal Health and Welfare, Faculty of Veterinary Medicine, University of Bari, Str. Prov. le per Casamassima Km 3, 70010, Valenzano (BA)</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">L.</namePart><namePart type="family">Passantino</namePart><affiliation>Department of Animal Health and Welfare, Faculty of Veterinary Medicine, University of Bari, Str. Prov. le per Casamassima Km 3, 70010, Valenzano (BA)</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">A.</namePart><namePart type="family">Perillo</namePart><affiliation>Department of Animal Health and Welfare, Faculty of Veterinary Medicine, University of Bari, Str. Prov. le per Casamassima Km 3, 70010, Valenzano (BA)</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">F.</namePart><namePart type="family">Jirillo</namePart><affiliation>Department of Internal Medicine, Immunology and Infectious Disease, Section of Microbiology and Immunology, Faculty of Medicine, University of Bari, Policlinico ‐Piazza G. Cesare‐ 70124 – Bari, Italy</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">M.</namePart><namePart type="family">Carrassi</namePart><affiliation>Department of Animal Health and Welfare, Faculty of Veterinary Medicine, University of Bari, Str. Prov. le per Casamassima Km 3, 70010, Valenzano (BA)</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">E.</namePart><namePart type="family">Jirillo</namePart><affiliation>Department of Animal Health and Welfare, Faculty of Veterinary Medicine, University of Bari, Str. Prov. le per Casamassima Km 3, 70010, Valenzano (BA)</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">G. F.</namePart><namePart type="family">Passantino</namePart><affiliation>Department of Animal Health and Welfare, Faculty of Veterinary Medicine, University of Bari, Str. Prov. le per Casamassima Km 3, 70010, Valenzano (BA)</affiliation><role><roleTerm type="text">author</roleTerm></role></name><typeOfResource>text</typeOfResource><genre type="abstract" displayLabel="abstract"></genre><originInfo><publisher>Blackwell Verlag GmbH</publisher><place><placeTerm type="text">Berlin, Germany</placeTerm></place><dateIssued encoding="w3cdtf">2005-12</dateIssued><copyrightDate encoding="w3cdtf">2005</copyrightDate></originInfo><language><languageTerm type="code" authority="rfc3066">en</languageTerm><languageTerm type="code" authority="iso639-2b">eng</languageTerm></language><physicalDescription><internetMediaType>text/html</internetMediaType></physicalDescription><abstract lang="en">Fish leukocyte heterogenity with respect to morphology, morphometry and immunological function has been object of some controversy, mostly because, in lower vertebrates, there are several interspecies differences. Leukocyte enzyme cytochemistry permits cellular differentiation, which is otherwise not possible with routine stains, and may also indicate cell function. In fish, phagocytic performance is principally operated by monocyte‐macrophages (MØ) present in tissues and in circulating blood. Fish thrombocytes (FTHR), even if they are the equivalent of platelets in mammals, are complete cells with cytoplasm and nucleus. They vary in shape from round, like small lymphocytes, to spindle‐shaped or rod‐shaped cells. Several cytochemical methods, as periodic acid Schiff (PAS), naphthol chloroacetate esterase (ASD), α‐naphthyl acetate esterase (ANAE), peroxidase (PEROX), acid phosphatase (Ac. Phos.) with and without tartaric acid (ta) and alkaline phosphatase (Alk. Phos.) have been applied in Salmo gairdneri Richardson to investigate the expression of MØ and FTHR enzyme patterns. Here, we compared cytochemistry between fish MØ and FTHR, and between human MØ and platelets/megakaryocytes, respectively, as indicated in the table. It appears that positivity to some enzyme cytochemistry is phylogenetically maintained in MØ, while in FTHR the enzyme pattern has undergone modification during evolution. For instance, this is the case of ANAE, Ac. Phos. and Alk. Phos., which changed in the phylogenesis, while PAS, AS‐D, PEROX are still present in the evolution. PAS AS‐D ANAE Perox Ac.Phos.‐ta Ac.Phos.+ta Alk. Phos Trout MØ ++ + ++ ++ + − n.d. Human MØ + + ++ + − − − Trout THR −/++ − − − −/+ − ++ Human platelets/ megakaryocytes + − ++ − + + − +, Positive; ++, strongly positive; (, negative; n.d., not determined.</abstract><relatedItem type="host"><titleInfo><title>Anatomia, Histologia, Embryologia</title></titleInfo><genre type="journal">journal</genre><identifier type="ISSN">0340-2096</identifier><identifier type="eISSN">1439-0264</identifier><identifier type="DOI">10.1111/(ISSN)1439-0264</identifier><identifier type="PublisherID">AHE</identifier><part><date>2005</date><detail type="volume"><caption>vol.</caption><number>34</number></detail><detail type="supplement"><caption>Suppl. no.</caption><number>s1</number></detail><extent unit="pages"><start>42</start><end>43</end></extent></part></relatedItem><identifier type="istex">919052E1E7FC92C14503EFE7A060F2EF8A9CD7AE</identifier><identifier type="DOI">10.1111/j.1439-0264.2005.00669_96.x</identifier><identifier type="ArticleID">AHE669_96_96</identifier><recordInfo><recordContentSource>WILEY</recordContentSource><recordOrigin>Blackwell Verlag GmbH</recordOrigin></recordInfo></mods></metadata><serie></serie></istex></record>Pour manipuler ce document sous Unix (Dilib)
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