Chloroplast DNA variation of white oak in the Baltic countries and Poland
Identifieur interne : 000122 ( PascalFrancis/Checkpoint ); précédent : 000121; suivant : 000123Chloroplast DNA variation of white oak in the Baltic countries and Poland
Auteurs : Ulrike M. Csaikl [Autriche] ; Izabela Glaz [France, Pologne] ; Virgilijus Baliuckas [Lituanie] ; Rémy J. Petit [France] ; Jan Svejgaard Jensene [Danemark]Source :
- Forest ecology and management [ 0378-1127 ] ; 2002.
Descripteurs français
- Pascal (Inist)
- Wicri :
- geographic : Estonie, Lettonie, Lituanie, Pologne.
- topic : Répartition géographique.
English descriptors
- KwdEn :
Abstract
In this study we were interested how recolonisation of oak in the Baltic region occurred after the last ice-age. To analyse the chloroplast DNA (cpDNA) variation for white oak species at the more northerly limit of their distribution, a total of 394 samples from 54 locations from Estonia, Latvia, Lithuania and Poland were assessed for previously characterised as well as newly found cpDNA variation. Of the oak samples taken, Quercus robur was most frequently found throughout the entire Baltic area. Quercus petraea was only found and characterised in Poland. A total of 13 different haplotypes were found within the Baltic area. Most frequent (75% of all samples) are members of lineage A (common in the Balkan refugial area) while 16% belong to oak from the Italian Pleistocene forest refuge and only a total of 9% originate in the Spanish refuge the majority of which is likely to be also allochtonous. Haplotype 7 of lineage A is found in 33% of the sample set in the entire Baltic region. Haplotype 6 is found at the more northern limit of the area. Haplotype 5 a more eastern member of the lineage is found at low frequency in the east of the region. Haplotype 4, rather sparse in Europe, is mainly scattered throughout Poland. Lineage C is represented by haplotypes 1 and 2 the former found close to the Baltic Sea while the latter, being an Eastern member of the lineage originating in Italy, is found at low frequency to the east of the region. Oak from refugial areas in Spain has limited impact on the area and is found exclusively in Poland. Such genotypes are found mainly close to the Baltic Sea in Poland and only 2% show up in uniform stands. Therefore members of lineage B could either have their most north-easterly limit of distribution in Poland or most likely they have been transferred there from possible German locations. In spite of the historical anthropogenic influences in the Baltic States as well as in Poland clear tracks of recolonisation could be identified.
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Pascal:02-0172688Le document en format XML
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Csaikl</name><affiliation wicri:level="1"><inist:fA14 i1="01"><s1>Austrian Research Centre Seibersdorf (ARCS)</s1><s2>2444 Seibersdorf</s2><s3>AUT</s3><sZ>1 aut.</sZ></inist:fA14><country>Autriche</country><wicri:noRegion>Austrian Research Centre Seibersdorf (ARCS)</wicri:noRegion></affiliation></author><author><name sortKey="Glaz, Izabela" sort="Glaz, Izabela" uniqKey="Glaz I" first="Izabela" last="Glaz">Izabela Glaz</name><affiliation wicri:level="3"><inist:fA14 i1="02"><s1>Institut National de la Recherche Agronomique, Station de Recherches Forestières, BP 45</s1><s2>33611 Gazinet</s2><s3>FRA</s3><sZ>2 aut.</sZ><sZ>4 aut.</sZ></inist:fA14><country>France</country><placeName><region type="region" nuts="2">Nouvelle-Aquitaine</region><region type="old region" nuts="2">Aquitaine</region><settlement type="city">Gazinet</settlement></placeName></affiliation><affiliation wicri:level="1"><inist:fA14 i1="03"><s1>Department of Genetics and Physiology of Woody Plants, Forest Research Institute, St. 3 Bitwy Warszawskiej 1920r</s1><s2>00 973 Warsaw</s2><s3>POL</s3><sZ>2 aut.</sZ></inist:fA14><country>Pologne</country><wicri:noRegion>00 973 Warsaw</wicri:noRegion></affiliation></author><author><name sortKey="Baliuckas, Virgilijus" sort="Baliuckas, Virgilijus" uniqKey="Baliuckas V" first="Virgilijus" last="Baliuckas">Virgilijus Baliuckas</name><affiliation wicri:level="1"><inist:fA14 i1="04"><s1>Department of Forest Genetics and Reforestation, Lithuanian Forest Research Institute</s1><s2>4312 Girionys</s2><s3>LTU</s3><sZ>3 aut.</sZ></inist:fA14><country>Lituanie</country><wicri:noRegion>4312 Girionys</wicri:noRegion></affiliation></author><author><name sortKey="Petit, Remy J" sort="Petit, Remy J" uniqKey="Petit R" first="Rémy J." last="Petit">Rémy J. Petit</name><affiliation wicri:level="3"><inist:fA14 i1="02"><s1>Institut National de la Recherche Agronomique, Station de Recherches Forestières, BP 45</s1><s2>33611 Gazinet</s2><s3>FRA</s3><sZ>2 aut.</sZ><sZ>4 aut.</sZ></inist:fA14><country>France</country><placeName><region type="region" nuts="2">Nouvelle-Aquitaine</region><region type="old region" nuts="2">Aquitaine</region><settlement type="city">Gazinet</settlement></placeName></affiliation></author><author><name sortKey="Jensene, Jan Svejgaard" sort="Jensene, Jan Svejgaard" uniqKey="Jensene J" first="Jan Svejgaard" last="Jensene">Jan Svejgaard Jensene</name><affiliation wicri:level="1"><inist:fA14 i1="05"><s1>Danish Forest and Landscape Research Institute, Hørsholm Kongevej</s1><s2>2970 Hørsholm</s2><s3>DNK</s3><sZ>5 aut.</sZ></inist:fA14><country>Danemark</country><wicri:noRegion>2970 Hørsholm</wicri:noRegion></affiliation></author></analytic><series><title level="j" type="main">Forest ecology and management</title><title level="j" type="abbreviated">For. ecol. manage.</title><idno type="ISSN">0378-1127</idno><imprint><date when="2002">2002</date></imprint></series></biblStruct></sourceDesc><seriesStmt><title level="j" type="main">Forest ecology and management</title><title level="j" type="abbreviated">For. ecol. manage.</title><idno type="ISSN">0378-1127</idno></seriesStmt></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Chloroplast DNA</term><term>Colonization</term><term>Estonia</term><term>Genetic diversity</term><term>Genetic variability</term><term>Geographic distribution</term><term>Glaciation</term><term>Haplotype</term><term>Latvia</term><term>Lithuania</term><term>Poland</term><term>Quercus petraea</term><term>Quercus robur</term><term>Refuge</term><term>Restriction fragment length polymorphism</term><term>Vegetation dynamics</term></keywords><keywords scheme="Pascal" xml:lang="fr"><term>DNA chloroplastique</term><term>Variabilité génétique</term><term>Diversité génétique</term><term>Colonisation</term><term>Dynamique végétation</term><term>Glaciation</term><term>Zone refuge</term><term>Répartition géographique</term><term>Haplotype</term><term>Quercus robur</term><term>Quercus petraea</term><term>Estonie</term><term>Lettonie</term><term>Lituanie</term><term>Pologne</term><term>Polymorphisme longueur fragment restriction</term></keywords><keywords scheme="Wicri" type="geographic" xml:lang="fr"><term>Estonie</term><term>Lettonie</term><term>Lituanie</term><term>Pologne</term></keywords><keywords scheme="Wicri" type="topic" xml:lang="fr"><term>Répartition géographique</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">In this study we were interested how recolonisation of oak in the Baltic region occurred after the last ice-age. To analyse the chloroplast DNA (cpDNA) variation for white oak species at the more northerly limit of their distribution, a total of 394 samples from 54 locations from Estonia, Latvia, Lithuania and Poland were assessed for previously characterised as well as newly found cpDNA variation. Of the oak samples taken, Quercus robur was most frequently found throughout the entire Baltic area. Quercus petraea was only found and characterised in Poland. A total of 13 different haplotypes were found within the Baltic area. Most frequent (75% of all samples) are members of lineage A (common in the Balkan refugial area) while 16% belong to oak from the Italian Pleistocene forest refuge and only a total of 9% originate in the Spanish refuge the majority of which is likely to be also allochtonous. Haplotype 7 of lineage A is found in 33% of the sample set in the entire Baltic region. Haplotype 6 is found at the more northern limit of the area. Haplotype 5 a more eastern member of the lineage is found at low frequency in the east of the region. Haplotype 4, rather sparse in Europe, is mainly scattered throughout Poland. Lineage C is represented by haplotypes 1 and 2 the former found close to the Baltic Sea while the latter, being an Eastern member of the lineage originating in Italy, is found at low frequency to the east of the region. Oak from refugial areas in Spain has limited impact on the area and is found exclusively in Poland. Such genotypes are found mainly close to the Baltic Sea in Poland and only 2% show up in uniform stands. Therefore members of lineage B could either have their most north-easterly limit of distribution in Poland or most likely they have been transferred there from possible German locations. In spite of the historical anthropogenic influences in the Baltic States as well as in Poland clear tracks of recolonisation could be identified.</div></front></TEI><inist><standard h6="B"><pA><fA01 i1="01" i2="1"><s0>0378-1127</s0></fA01><fA02 i1="01"><s0>FECMDW</s0></fA02><fA03 i2="1"><s0>For. ecol. manage.</s0></fA03><fA05><s2>156</s2></fA05><fA06><s2>1-3</s2></fA06><fA08 i1="01" i2="1" l="ENG"><s1>Chloroplast DNA variation of white oak in the Baltic countries and Poland</s1></fA08><fA09 i1="01" i2="1" l="ENG"><s1>Range wide distribution of chloroplast DNA diversity and pollen deposits in European white oaks: inferences about colonisation routes and management of oak genetic resources</s1></fA09><fA11 i1="01" i2="1"><s1>CSAIKL (Ulrike M.)</s1></fA11><fA11 i1="02" i2="1"><s1>GLAZ (Izabela)</s1></fA11><fA11 i1="03" i2="1"><s1>BALIUCKAS (Virgilijus)</s1></fA11><fA11 i1="04" i2="1"><s1>PETIT (Rémy J.)</s1></fA11><fA11 i1="05" i2="1"><s1>JENSENE (Jan Svejgaard)</s1></fA11><fA12 i1="01" i2="1"><s1>KREMER (Antoine)</s1><s9>ed.</s9></fA12><fA12 i1="02" i2="1"><s1>GOENAGA (Xabier)</s1><s9>préf.</s9></fA12><fA14 i1="01"><s1>Austrian Research Centre Seibersdorf (ARCS)</s1><s2>2444 Seibersdorf</s2><s3>AUT</s3><sZ>1 aut.</sZ></fA14><fA14 i1="02"><s1>Institut National de la Recherche Agronomique, Station de Recherches Forestières, BP 45</s1><s2>33611 Gazinet</s2><s3>FRA</s3><sZ>2 aut.</sZ><sZ>4 aut.</sZ></fA14><fA14 i1="03"><s1>Department of Genetics and Physiology of Woody Plants, Forest Research Institute, St. 3 Bitwy Warszawskiej 1920r</s1><s2>00 973 Warsaw</s2><s3>POL</s3><sZ>2 aut.</sZ></fA14><fA14 i1="04"><s1>Department of Forest Genetics and Reforestation, Lithuanian Forest Research Institute</s1><s2>4312 Girionys</s2><s3>LTU</s3><sZ>3 aut.</sZ></fA14><fA14 i1="05"><s1>Danish Forest and Landscape Research Institute, Hørsholm Kongevej</s1><s2>2970 Hørsholm</s2><s3>DNK</s3><sZ>5 aut.</sZ></fA14><fA15 i1="01"><s1>Institut National de la Recherche Agronomique, Station de Recherches Forestières, BP 45</s1><s2>33611 Gazinet</s2><s3>FRA</s3></fA15><fA15 i1="02"><s1>Directorate General for Research, European Commission, Rue de la Loi 200</s1><s2>1049 Brussels</s2><s3>BEL</s3><sZ>2 aut.</sZ></fA15><fA20><s1>211-222</s1></fA20><fA21><s1>2002</s1></fA21><fA23 i1="01"><s0>ENG</s0></fA23><fA43 i1="01"><s1>INIST</s1><s2>17223</s2><s5>354000102308950130</s5></fA43><fA44><s0>0000</s0><s1>© 2002 INIST-CNRS. All rights reserved.</s1></fA44><fA45><s0>1 p.1/4</s0></fA45><fA47 i1="01" i2="1"><s0>02-0172688</s0></fA47><fA60><s1>P</s1></fA60><fA61><s0>A</s0></fA61><fA64 i1="01" i2="1"><s0>Forest ecology and management</s0></fA64><fA66 i1="01"><s0>NLD</s0></fA66><fC01 i1="01" l="ENG"><s0>In this study we were interested how recolonisation of oak in the Baltic region occurred after the last ice-age. To analyse the chloroplast DNA (cpDNA) variation for white oak species at the more northerly limit of their distribution, a total of 394 samples from 54 locations from Estonia, Latvia, Lithuania and Poland were assessed for previously characterised as well as newly found cpDNA variation. Of the oak samples taken, Quercus robur was most frequently found throughout the entire Baltic area. Quercus petraea was only found and characterised in Poland. A total of 13 different haplotypes were found within the Baltic area. Most frequent (75% of all samples) are members of lineage A (common in the Balkan refugial area) while 16% belong to oak from the Italian Pleistocene forest refuge and only a total of 9% originate in the Spanish refuge the majority of which is likely to be also allochtonous. Haplotype 7 of lineage A is found in 33% of the sample set in the entire Baltic region. Haplotype 6 is found at the more northern limit of the area. Haplotype 5 a more eastern member of the lineage is found at low frequency in the east of the region. Haplotype 4, rather sparse in Europe, is mainly scattered throughout Poland. Lineage C is represented by haplotypes 1 and 2 the former found close to the Baltic Sea while the latter, being an Eastern member of the lineage originating in Italy, is found at low frequency to the east of the region. Oak from refugial areas in Spain has limited impact on the area and is found exclusively in Poland. Such genotypes are found mainly close to the Baltic Sea in Poland and only 2% show up in uniform stands. Therefore members of lineage B could either have their most north-easterly limit of distribution in Poland or most likely they have been transferred there from possible German locations. In spite of the historical anthropogenic influences in the Baltic States as well as in Poland clear tracks of recolonisation could be identified.</s0></fC01><fC02 i1="01" i2="X"><s0>002A32D01B3</s0></fC02><fC02 i1="02" i2="X"><s0>002A33C02</s0></fC02><fC03 i1="01" i2="X" l="FRE"><s0>DNA chloroplastique</s0><s5>01</s5></fC03><fC03 i1="01" i2="X" l="ENG"><s0>Chloroplast DNA</s0><s5>01</s5></fC03><fC03 i1="01" i2="X" l="SPA"><s0>DNA cloroplástico</s0><s5>01</s5></fC03><fC03 i1="02" i2="X" l="FRE"><s0>Variabilité génétique</s0><s5>02</s5></fC03><fC03 i1="02" i2="X" l="ENG"><s0>Genetic variability</s0><s5>02</s5></fC03><fC03 i1="02" i2="X" l="SPA"><s0>Variabilidad genética</s0><s5>02</s5></fC03><fC03 i1="03" i2="X" l="FRE"><s0>Diversité génétique</s0><s5>03</s5></fC03><fC03 i1="03" i2="X" l="ENG"><s0>Genetic diversity</s0><s5>03</s5></fC03><fC03 i1="03" i2="X" l="SPA"><s0>Diversidad genética</s0><s5>03</s5></fC03><fC03 i1="04" i2="X" l="FRE"><s0>Colonisation</s0><s5>04</s5></fC03><fC03 i1="04" i2="X" l="ENG"><s0>Colonization</s0><s5>04</s5></fC03><fC03 i1="04" i2="X" l="SPA"><s0>Colonización</s0><s5>04</s5></fC03><fC03 i1="05" i2="X" l="FRE"><s0>Dynamique végétation</s0><s5>05</s5></fC03><fC03 i1="05" i2="X" l="ENG"><s0>Vegetation dynamics</s0><s5>05</s5></fC03><fC03 i1="05" i2="X" l="SPA"><s0>Dinámica vegetación</s0><s5>05</s5></fC03><fC03 i1="06" i2="X" l="FRE"><s0>Glaciation</s0><s5>06</s5></fC03><fC03 i1="06" i2="X" l="ENG"><s0>Glaciation</s0><s5>06</s5></fC03><fC03 i1="06" i2="X" l="SPA"><s0>Glaciación</s0><s5>06</s5></fC03><fC03 i1="07" i2="X" l="FRE"><s0>Zone refuge</s0><s5>07</s5></fC03><fC03 i1="07" i2="X" l="ENG"><s0>Refuge</s0><s5>07</s5></fC03><fC03 i1="07" i2="X" l="SPA"><s0>Zona refugio</s0><s5>07</s5></fC03><fC03 i1="08" i2="X" l="FRE"><s0>Répartition géographique</s0><s5>08</s5></fC03><fC03 i1="08" i2="X" l="ENG"><s0>Geographic distribution</s0><s5>08</s5></fC03><fC03 i1="08" i2="X" l="SPA"><s0>Distribución geográfica</s0><s5>08</s5></fC03><fC03 i1="09" i2="X" l="FRE"><s0>Haplotype</s0><s5>09</s5></fC03><fC03 i1="09" i2="X" l="ENG"><s0>Haplotype</s0><s5>09</s5></fC03><fC03 i1="09" i2="X" l="SPA"><s0>Haplotipo</s0><s5>09</s5></fC03><fC03 i1="10" i2="X" l="FRE"><s0>Quercus robur</s0><s2>NS</s2><s5>10</s5></fC03><fC03 i1="10" i2="X" l="ENG"><s0>Quercus robur</s0><s2>NS</s2><s5>10</s5></fC03><fC03 i1="10" i2="X" l="SPA"><s0>Quercus robur</s0><s2>NS</s2><s5>10</s5></fC03><fC03 i1="11" i2="X" l="FRE"><s0>Quercus petraea</s0><s2>NS</s2><s5>11</s5></fC03><fC03 i1="11" i2="X" l="ENG"><s0>Quercus petraea</s0><s2>NS</s2><s5>11</s5></fC03><fC03 i1="11" i2="X" l="SPA"><s0>Quercus petraea</s0><s2>NS</s2><s5>11</s5></fC03><fC03 i1="12" i2="X" l="FRE"><s0>Estonie</s0><s2>NG</s2><s5>20</s5></fC03><fC03 i1="12" i2="X" l="ENG"><s0>Estonia</s0><s2>NG</s2><s5>20</s5></fC03><fC03 i1="12" i2="X" l="SPA"><s0>Estonia</s0><s2>NG</s2><s5>20</s5></fC03><fC03 i1="13" i2="X" l="FRE"><s0>Lettonie</s0><s2>NG</s2><s5>21</s5></fC03><fC03 i1="13" i2="X" l="ENG"><s0>Latvia</s0><s2>NG</s2><s5>21</s5></fC03><fC03 i1="13" i2="X" l="SPA"><s0>Letonia</s0><s2>NG</s2><s5>21</s5></fC03><fC03 i1="14" i2="X" l="FRE"><s0>Lituanie</s0><s2>NG</s2><s5>22</s5></fC03><fC03 i1="14" i2="X" l="ENG"><s0>Lithuania</s0><s2>NG</s2><s5>22</s5></fC03><fC03 i1="14" i2="X" l="SPA"><s0>Lituania</s0><s2>NG</s2><s5>22</s5></fC03><fC03 i1="15" i2="X" l="FRE"><s0>Pologne</s0><s2>NG</s2><s5>23</s5></fC03><fC03 i1="15" i2="X" l="ENG"><s0>Poland</s0><s2>NG</s2><s5>23</s5></fC03><fC03 i1="15" i2="X" l="SPA"><s0>Polonia</s0><s2>NG</s2><s5>23</s5></fC03><fC03 i1="16" i2="X" l="FRE"><s0>Polymorphisme longueur fragment restriction</s0><s5>33</s5></fC03><fC03 i1="16" i2="X" l="ENG"><s0>Restriction fragment length polymorphism</s0><s5>33</s5></fC03><fC03 i1="16" i2="X" l="SPA"><s0>Polimorfismo longitud fragmento restricción</s0><s5>33</s5></fC03><fC07 i1="01" i2="X" l="FRE"><s0>Fagaceae</s0><s2>NS</s2></fC07><fC07 i1="01" i2="X" l="ENG"><s0>Fagaceae</s0><s2>NS</s2></fC07><fC07 i1="01" i2="X" l="SPA"><s0>Fagaceae</s0><s2>NS</s2></fC07><fC07 i1="02" i2="X" l="FRE"><s0>Dicotyledones</s0><s2>NS</s2></fC07><fC07 i1="02" i2="X" l="ENG"><s0>Dicotyledones</s0><s2>NS</s2></fC07><fC07 i1="02" i2="X" l="SPA"><s0>Dicotyledones</s0><s2>NS</s2></fC07><fC07 i1="03" i2="X" l="FRE"><s0>Angiospermae</s0><s2>NS</s2></fC07><fC07 i1="03" i2="X" l="ENG"><s0>Angiospermae</s0><s2>NS</s2></fC07><fC07 i1="03" i2="X" l="SPA"><s0>Angiospermae</s0><s2>NS</s2></fC07><fC07 i1="04" i2="X" l="FRE"><s0>Spermatophyta</s0><s2>NS</s2></fC07><fC07 i1="04" i2="X" l="ENG"><s0>Spermatophyta</s0><s2>NS</s2></fC07><fC07 i1="04" i2="X" l="SPA"><s0>Spermatophyta</s0><s2>NS</s2></fC07><fC07 i1="05" i2="X" l="FRE"><s0>Europe Est</s0><s2>NG</s2></fC07><fC07 i1="05" i2="X" l="ENG"><s0>Eastern Europe</s0><s2>NG</s2></fC07><fC07 i1="05" i2="X" l="SPA"><s0>Europa del Este</s0><s2>NG</s2></fC07><fC07 i1="06" i2="X" l="FRE"><s0>Europe</s0><s2>NG</s2></fC07><fC07 i1="06" i2="X" l="ENG"><s0>Europe</s0><s2>NG</s2></fC07><fC07 i1="06" i2="X" l="SPA"><s0>Europa</s0><s2>NG</s2></fC07><fC07 i1="07" i2="X" l="FRE"><s0>Arbre forestier feuillu</s0><s5>39</s5></fC07><fC07 i1="07" i2="X" l="ENG"><s0>Hardwood forest tree</s0><s5>39</s5></fC07><fC07 i1="07" i2="X" l="SPA"><s0>Arbol forestal frondoso</s0><s5>39</s5></fC07><fN21><s1>098</s1></fN21><fN82><s1>PSI</s1></fN82></pA></standard></inist><affiliations><list><country><li>Autriche</li><li>Danemark</li><li>France</li><li>Lituanie</li><li>Pologne</li></country><region><li>Aquitaine</li><li>Nouvelle-Aquitaine</li></region><settlement><li>Gazinet</li></settlement></list><tree><country name="Autriche"><noRegion><name sortKey="Csaikl, Ulrike M" sort="Csaikl, Ulrike M" uniqKey="Csaikl U" first="Ulrike M." last="Csaikl">Ulrike M. Csaikl</name></noRegion></country><country name="France"><region name="Nouvelle-Aquitaine"><name sortKey="Glaz, Izabela" sort="Glaz, Izabela" uniqKey="Glaz I" first="Izabela" last="Glaz">Izabela Glaz</name></region><name sortKey="Petit, Remy J" sort="Petit, Remy J" uniqKey="Petit R" first="Rémy J." last="Petit">Rémy J. Petit</name></country><country name="Pologne"><noRegion><name sortKey="Glaz, Izabela" sort="Glaz, Izabela" uniqKey="Glaz I" first="Izabela" last="Glaz">Izabela Glaz</name></noRegion></country><country name="Lituanie"><noRegion><name sortKey="Baliuckas, Virgilijus" sort="Baliuckas, Virgilijus" uniqKey="Baliuckas V" first="Virgilijus" last="Baliuckas">Virgilijus Baliuckas</name></noRegion></country><country name="Danemark"><noRegion><name sortKey="Jensene, Jan Svejgaard" sort="Jensene, Jan Svejgaard" uniqKey="Jensene J" first="Jan Svejgaard" last="Jensene">Jan Svejgaard Jensene</name></noRegion></country></tree></affiliations></record>Pour manipuler ce document sous Unix (Dilib)
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