AustralieFrV1, PascalFrancis, Corpus, bibRecord, 002E87

Out of the Palaeotropics? Historical biogeography and diversification of the cosmopolitan ectomycorrhizal mushroom family Inocybaceae

Identifieur interne : 002E87 ( PascalFrancis/Corpus ); précédent : 002E86; suivant : 002E88

Out of the Palaeotropics? Historical biogeography and diversification of the cosmopolitan ectomycorrhizal mushroom family Inocybaceae

Auteurs : P. Brandon Matheny ; M. Catherine Aime ; Neale L. Bougher ; Bart Buyck ; Dennis E. Desjardin ; Egon Horak ; Bradley R. Kropp ; D. Jean Lodge ; Kasem Soytong ; James M. Trappe ; David S. Hibbett

Source :

Journal of biogeography [ 0305-0270 ] ; 2009.

RBID : Pascal:09-0163619

Descripteurs français

Pascal (Inist)
- Historique, Biogéographie, Diversification, Dispersion, Ectomycorhize, Horloge moléculaire, Vicariance, Fungi, Basidiomycota.

English descriptors

KwdEn :
- Basidiomycota, Biogeography, Case history, Dispersion, Diversification, Ectomycorrhiza, Fungi, Molecular clock, Vicariance.

Abstract

Aim The ectomycorrhizal (ECM) mushroom family Inocybaceae is widespread in north temperate regions, but more than 150 species are encountered in the tropics and the Southern Hemisphere. The relative roles of recent and ancient biogeographical processes, relationships with plant hosts, and the timing of divergences that have shaped the current geographic distribution of the family are investigated. Location Africa, Australia, Neotropics, New Zealand, north temperate zone, Palaeotropics, Southeast Asia, South America, south temperate zone. Methods We reconstruct a phylogeny of the Inocybaceae with a geological timeline using a relaxed molecular clock. Divergence dates of lineages are estimated statistically to test vicariance-based hypotheses concerning relatedness of disjunct ECM taxa. A series of internal maximum time constraints is used to evaluate two different calibrations. Ancestral state reconstruction is used to infer ancestral areas and ancestral plant partners of the family. Results The Palaeotropics are unique in containing representatives of all major clades of Inocybaceae. Six of the seven major clades diversified initially during the Cretaceous, with subsequent radiations probably during the early Palaeogene. Vicariance patterns cannot be rejected that involve area relationships for Africa-Australia, Africa-India and southern South America-Australia. Northern and southern South America, Australia and New Zealand are primarily the recipients of immigrant taxa during the Palaeogene or later. Angiosperms were the earliest hosts of Inocybaceae. Transitions to conifers probably occurred no earlier than 65 Ma. Main conclusions The Inocybaceae initially diversified no later than the Cretaceous in Palaeotropical settings, in association with angiosperms. Diversification within major clades of the family accelerated during the Palaeogene in north and south temperate regions, whereas several relictual lineages persisted in the tropics. Both vicariance and dispersal patterns are detected. Species from Neotropical and south temperate regions are largely derived from immigrant ancestors from north temperate or Palaeotropical regions. Transitions to conifer hosts occurred later, probably during the Palaeogene.

Notice en format standard (ISO 2709)

Pour connaître la documentation sur le format Inist Standard.

A01	`01`	`1`		`@0 0305-0270`
A02	`01`			`@0 JBIODN`
A03		`1`		`@0 J. biogeogr.`
A05				`@2 36`
A06				`@2 4`
A08	`01`	`1`	`ENG`	`@1 Out of the Palaeotropics? Historical biogeography and diversification of the cosmopolitan ectomycorrhizal mushroom family Inocybaceae`
A11	`01`	`1`		`@1 BRANDON MATHENY (P.)`
A11	`02`	`1`		`@1 AIME (M. Catherine)`
A11	`03`	`1`		`@1 BOUGHER (Neale L.)`
A11	`04`	`1`		`@1 BUYCK (Bart)`
A11	`05`	`1`		`@1 DESJARDIN (Dennis E.)`
A11	`06`	`1`		`@1 HORAK (Egon)`
A11	`07`	`1`		`@1 KROPP (Bradley R.)`
A11	`08`	`1`		`@1 LODGE (D. Jean)`
A11	`09`	`1`		`@1 SOYTONG (Kasem)`
A11	`10`	`1`		`@1 TRAPPE (James M.)`
A11	`11`	`1`		`@1 HIBBETT (David S.)`
A14	`01`			`@1 Biology Department, Clark University @2 Worcester, MA @3 USA @Z 1 aut. @Z 11 aut.`
A14	`02`			`@1 Department of Plant Pathology and Crop Physiology, Louisiana State University Agricultural Center @2 Baton Rouge, LA @3 USA @Z 2 aut.`
A14	`03`			`@1 Department of Environment and Conservation, Western Australian Herbarium, Bentley Delivery Centre @2 Perth, WA @3 AUS @Z 3 aut.`
A14	`04`			`@1 Muséum National d'Histoire Naturelle, Département Systématique et Evolution, USM 602 -CP 39 @2 Paris @3 FRA @Z 4 aut.`
A14	`05`			`@1 Department of Biology, San Francisco State University @2 San Francisco, CA @3 USA @Z 5 aut.`
A14	`06`			`@1 Nikodemweg 5 @2 Innsbruck @3 AUT @Z 6 aut.`
A14	`07`			`@1 Department of Biology, Utah State University @2 Logan, UT @3 USA @Z 7 aut.`
A14	`08`			`@1 Center for Forest Mycology Research, US Department of Agriculture, Forest Service, Northern Research Station @2 Luquillo @3 PRI @Z 8 aut.`
A14	`09`			`@1 Faculty of Agricultural Technology, King Mongkut's Institute of Technology Ladkrabang @2 Bangkok @3 THA @Z 9 aut.`
A14	`10`			`@1 Department of Forest Science, Oregon State University @2 Corvallis, OR @3 USA @Z 10 aut.`
A20				`@1 577-592`
A21				`@1 2009`
A23	`01`			`@0 ENG`
A43	`01`			`@1 INIST @2 15698 @5 354000184838010020`
A44				`@0 0000 @1 © 2009 INIST-CNRS. All rights reserved.`
A45				`@0 3 p.1/4`
A47	`01`	`1`		`@0 09-0163619`
A60				`@1 P`
A61				`@0 A`
A64	`01`	`1`		`@0 Journal of biogeography`
A66	`01`			`@0 GBR`
C01	`01`		`ENG`	@0 Aim The ectomycorrhizal (ECM) mushroom family Inocybaceae is widespread in north temperate regions, but more than 150 species are encountered in the tropics and the Southern Hemisphere. The relative roles of recent and ancient biogeographical processes, relationships with plant hosts, and the timing of divergences that have shaped the current geographic distribution of the family are investigated. Location Africa, Australia, Neotropics, New Zealand, north temperate zone, Palaeotropics, Southeast Asia, South America, south temperate zone. Methods We reconstruct a phylogeny of the Inocybaceae with a geological timeline using a relaxed molecular clock. Divergence dates of lineages are estimated statistically to test vicariance-based hypotheses concerning relatedness of disjunct ECM taxa. A series of internal maximum time constraints is used to evaluate two different calibrations. Ancestral state reconstruction is used to infer ancestral areas and ancestral plant partners of the family. Results The Palaeotropics are unique in containing representatives of all major clades of Inocybaceae. Six of the seven major clades diversified initially during the Cretaceous, with subsequent radiations probably during the early Palaeogene. Vicariance patterns cannot be rejected that involve area relationships for Africa-Australia, Africa-India and southern South America-Australia. Northern and southern South America, Australia and New Zealand are primarily the recipients of immigrant taxa during the Palaeogene or later. Angiosperms were the earliest hosts of Inocybaceae. Transitions to conifers probably occurred no earlier than 65 Ma. Main conclusions The Inocybaceae initially diversified no later than the Cretaceous in Palaeotropical settings, in association with angiosperms. Diversification within major clades of the family accelerated during the Palaeogene in north and south temperate regions, whereas several relictual lineages persisted in the tropics. Both vicariance and dispersal patterns are detected. Species from Neotropical and south temperate regions are largely derived from immigrant ancestors from north temperate or Palaeotropical regions. Transitions to conifer hosts occurred later, probably during the Palaeogene.
C02	`01`	`X`		`@0 002A14B04A`
C03	`01`	`X`	`FRE`	`@0 Historique @5 01`
C03	`01`	`X`	`ENG`	`@0 Case history @5 01`
C03	`01`	`X`	`SPA`	`@0 Estudio histórico @5 01`
C03	`02`	`X`	`FRE`	`@0 Biogéographie @5 02`
C03	`02`	`X`	`ENG`	`@0 Biogeography @5 02`
C03	`02`	`X`	`SPA`	`@0 Biogeografía @5 02`
C03	`03`	`X`	`FRE`	`@0 Diversification @5 03`
C03	`03`	`X`	`ENG`	`@0 Diversification @5 03`
C03	`03`	`X`	`SPA`	`@0 Diversificación @5 03`
C03	`04`	`X`	`FRE`	`@0 Dispersion @5 04`
C03	`04`	`X`	`ENG`	`@0 Dispersion @5 04`
C03	`04`	`X`	`SPA`	`@0 Dispersión @5 04`
C03	`05`	`X`	`FRE`	`@0 Ectomycorhize @5 05`
C03	`05`	`X`	`ENG`	`@0 Ectomycorrhiza @5 05`
C03	`05`	`X`	`SPA`	`@0 Ectomicorriza @5 05`
C03	`06`	`X`	`FRE`	`@0 Horloge moléculaire @5 06`
C03	`06`	`X`	`ENG`	`@0 Molecular clock @5 06`
C03	`06`	`X`	`SPA`	`@0 Reloj molecular @5 06`
C03	`07`	`X`	`FRE`	`@0 Vicariance @5 07`
C03	`07`	`X`	`ENG`	`@0 Vicariance @5 07`
C03	`07`	`X`	`SPA`	`@0 Vicariancia @5 07`
C03	`08`	`X`	`FRE`	`@0 Fungi @2 NS @5 49`
C03	`08`	`X`	`ENG`	`@0 Fungi @2 NS @5 49`
C03	`08`	`X`	`SPA`	`@0 Fungi @2 NS @5 49`
C03	`09`	`X`	`FRE`	`@0 Basidiomycota @2 NS @5 50`
C03	`09`	`X`	`ENG`	`@0 Basidiomycota @2 NS @5 50`
C03	`09`	`X`	`SPA`	`@0 Basidiomycota @2 NS @5 50`
C07	`01`	`X`	`FRE`	`@0 Mycorhize`
C07	`01`	`X`	`ENG`	`@0 Mycorrhiza`
C07	`01`	`X`	`SPA`	`@0 Micorriza`
C07	`02`	`X`	`FRE`	`@0 Symbionte @5 17`
C07	`02`	`X`	`ENG`	`@0 Symbiont @5 17`
C07	`02`	`X`	`SPA`	`@0 Simbionte @5 17`
N21				`@1 117`
N44	`01`			`@1 OTO`
N82				`@1 OTO`

Format Inist (serveur)

NO :	PASCAL 09-0163619 INIST
ET :	Out of the Palaeotropics? Historical biogeography and diversification of the cosmopolitan ectomycorrhizal mushroom family Inocybaceae
AU :	BRANDON MATHENY (P.); AIME (M. Catherine); BOUGHER (Neale L.); BUYCK (Bart); DESJARDIN (Dennis E.); HORAK (Egon); KROPP (Bradley R.); LODGE (D. Jean); SOYTONG (Kasem); TRAPPE (James M.); HIBBETT (David S.)
AF :	Biology Department, Clark University/Worcester, MA/Etats-Unis (1 aut., 11 aut.); Department of Plant Pathology and Crop Physiology, Louisiana State University Agricultural Center/Baton Rouge, LA/Etats-Unis (2 aut.); Department of Environment and Conservation, Western Australian Herbarium, Bentley Delivery Centre/Perth, WA/Australie (3 aut.); Muséum National d'Histoire Naturelle, Département Systématique et Evolution, USM 602 -CP 39/Paris/France (4 aut.); Department of Biology, San Francisco State University/San Francisco, CA/Etats-Unis (5 aut.); Nikodemweg 5/Innsbruck/Autriche (6 aut.); Department of Biology, Utah State University/Logan, UT/Etats-Unis (7 aut.); Center for Forest Mycology Research, US Department of Agriculture, Forest Service, Northern Research Station/Luquillo/Porto Rico (8 aut.); Faculty of Agricultural Technology, King Mongkut's Institute of Technology Ladkrabang/Bangkok/Thaïlande (9 aut.); Department of Forest Science, Oregon State University/Corvallis, OR/Etats-Unis (10 aut.)
DT :	Publication en série; Niveau analytique
SO :	Journal of biogeography; ISSN 0305-0270; Coden JBIODN; Royaume-Uni; Da. 2009; Vol. 36; No. 4; Pp. 577-592; Bibl. 3 p.1/4
LA :	Anglais
EA :	Aim The ectomycorrhizal (ECM) mushroom family Inocybaceae is widespread in north temperate regions, but more than 150 species are encountered in the tropics and the Southern Hemisphere. The relative roles of recent and ancient biogeographical processes, relationships with plant hosts, and the timing of divergences that have shaped the current geographic distribution of the family are investigated. Location Africa, Australia, Neotropics, New Zealand, north temperate zone, Palaeotropics, Southeast Asia, South America, south temperate zone. Methods We reconstruct a phylogeny of the Inocybaceae with a geological timeline using a relaxed molecular clock. Divergence dates of lineages are estimated statistically to test vicariance-based hypotheses concerning relatedness of disjunct ECM taxa. A series of internal maximum time constraints is used to evaluate two different calibrations. Ancestral state reconstruction is used to infer ancestral areas and ancestral plant partners of the family. Results The Palaeotropics are unique in containing representatives of all major clades of Inocybaceae. Six of the seven major clades diversified initially during the Cretaceous, with subsequent radiations probably during the early Palaeogene. Vicariance patterns cannot be rejected that involve area relationships for Africa-Australia, Africa-India and southern South America-Australia. Northern and southern South America, Australia and New Zealand are primarily the recipients of immigrant taxa during the Palaeogene or later. Angiosperms were the earliest hosts of Inocybaceae. Transitions to conifers probably occurred no earlier than 65 Ma. Main conclusions The Inocybaceae initially diversified no later than the Cretaceous in Palaeotropical settings, in association with angiosperms. Diversification within major clades of the family accelerated during the Palaeogene in north and south temperate regions, whereas several relictual lineages persisted in the tropics. Both vicariance and dispersal patterns are detected. Species from Neotropical and south temperate regions are largely derived from immigrant ancestors from north temperate or Palaeotropical regions. Transitions to conifer hosts occurred later, probably during the Palaeogene.
CC :	002A14B04A
FD :	Historique; Biogéographie; Diversification; Dispersion; Ectomycorhize; Horloge moléculaire; Vicariance; Fungi; Basidiomycota
FG :	Mycorhize; Symbionte
ED :	Case history; Biogeography; Diversification; Dispersion; Ectomycorrhiza; Molecular clock; Vicariance; Fungi; Basidiomycota
EG :	Mycorrhiza; Symbiont
SD :	Estudio histórico; Biogeografía; Diversificación; Dispersión; Ectomicorriza; Reloj molecular; Vicariancia; Fungi; Basidiomycota
LO :	INIST-15698.354000184838010020
ID :	09-0163619

Links to Exploration step

Pascal:09-0163619

Le document en format XML

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<author><name sortKey="Trappe, James M" sort="Trappe, James M" uniqKey="Trappe J" first="James M." last="Trappe">James M. Trappe</name>
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<author><name sortKey="Hibbett, David S" sort="Hibbett, David S" uniqKey="Hibbett D" first="David S." last="Hibbett">David S. Hibbett</name>
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<sourceDesc><biblStruct><analytic><title xml:lang="en" level="a">Out of the Palaeotropics? Historical biogeography and diversification of the cosmopolitan ectomycorrhizal mushroom family Inocybaceae</title>
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<author><name sortKey="Desjardin, Dennis E" sort="Desjardin, Dennis E" uniqKey="Desjardin D" first="Dennis E." last="Desjardin">Dennis E. Desjardin</name>
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<author><name sortKey="Horak, Egon" sort="Horak, Egon" uniqKey="Horak E" first="Egon" last="Horak">Egon Horak</name>
<affiliation><inist:fA14 i1="06"><s1>Nikodemweg 5</s1>
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<author><name sortKey="Kropp, Bradley R" sort="Kropp, Bradley R" uniqKey="Kropp B" first="Bradley R." last="Kropp">Bradley R. Kropp</name>
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<s2>Logan, UT</s2>
<s3>USA</s3>
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<author><name sortKey="Lodge, D Jean" sort="Lodge, D Jean" uniqKey="Lodge D" first="D. Jean" last="Lodge">D. Jean Lodge</name>
<affiliation><inist:fA14 i1="08"><s1>Center for Forest Mycology Research, US Department of Agriculture, Forest Service, Northern Research Station</s1>
<s2>Luquillo</s2>
<s3>PRI</s3>
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<author><name sortKey="Soytong, Kasem" sort="Soytong, Kasem" uniqKey="Soytong K" first="Kasem" last="Soytong">Kasem Soytong</name>
<affiliation><inist:fA14 i1="09"><s1>Faculty of Agricultural Technology, King Mongkut's Institute of Technology Ladkrabang</s1>
<s2>Bangkok</s2>
<s3>THA</s3>
<sZ>9 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author><name sortKey="Trappe, James M" sort="Trappe, James M" uniqKey="Trappe J" first="James M." last="Trappe">James M. Trappe</name>
<affiliation><inist:fA14 i1="10"><s1>Department of Forest Science, Oregon State University</s1>
<s2>Corvallis, OR</s2>
<s3>USA</s3>
<sZ>10 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author><name sortKey="Hibbett, David S" sort="Hibbett, David S" uniqKey="Hibbett D" first="David S." last="Hibbett">David S. Hibbett</name>
<affiliation><inist:fA14 i1="01"><s1>Biology Department, Clark University</s1>
<s2>Worcester, MA</s2>
<s3>USA</s3>
<sZ>1 aut.</sZ>
<sZ>11 aut.</sZ>
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<series><title level="j" type="main">Journal of biogeography</title>
<title level="j" type="abbreviated">J. biogeogr.</title>
<idno type="ISSN">0305-0270</idno>
<imprint><date when="2009">2009</date>
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<seriesStmt><title level="j" type="main">Journal of biogeography</title>
<title level="j" type="abbreviated">J. biogeogr.</title>
<idno type="ISSN">0305-0270</idno>
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<profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Basidiomycota</term>
<term>Biogeography</term>
<term>Case history</term>
<term>Dispersion</term>
<term>Diversification</term>
<term>Ectomycorrhiza</term>
<term>Fungi</term>
<term>Molecular clock</term>
<term>Vicariance</term>
</keywords>
<keywords scheme="Pascal" xml:lang="fr"><term>Historique</term>
<term>Biogéographie</term>
<term>Diversification</term>
<term>Dispersion</term>
<term>Ectomycorhize</term>
<term>Horloge moléculaire</term>
<term>Vicariance</term>
<term>Fungi</term>
<term>Basidiomycota</term>
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<front><div type="abstract" xml:lang="en">Aim The ectomycorrhizal (ECM) mushroom family Inocybaceae is widespread in north temperate regions, but more than 150 species are encountered in the tropics and the Southern Hemisphere. The relative roles of recent and ancient biogeographical processes, relationships with plant hosts, and the timing of divergences that have shaped the current geographic distribution of the family are investigated. Location Africa, Australia, Neotropics, New Zealand, north temperate zone, Palaeotropics, Southeast Asia, South America, south temperate zone. Methods We reconstruct a phylogeny of the Inocybaceae with a geological timeline using a relaxed molecular clock. Divergence dates of lineages are estimated statistically to test vicariance-based hypotheses concerning relatedness of disjunct ECM taxa. A series of internal maximum time constraints is used to evaluate two different calibrations. Ancestral state reconstruction is used to infer ancestral areas and ancestral plant partners of the family. Results The Palaeotropics are unique in containing representatives of all major clades of Inocybaceae. Six of the seven major clades diversified initially during the Cretaceous, with subsequent radiations probably during the early Palaeogene. Vicariance patterns cannot be rejected that involve area relationships for Africa-Australia, Africa-India and southern South America-Australia. Northern and southern South America, Australia and New Zealand are primarily the recipients of immigrant taxa during the Palaeogene or later. Angiosperms were the earliest hosts of Inocybaceae. Transitions to conifers probably occurred no earlier than 65 Ma. Main conclusions The Inocybaceae initially diversified no later than the Cretaceous in Palaeotropical settings, in association with angiosperms. Diversification within major clades of the family accelerated during the Palaeogene in north and south temperate regions, whereas several relictual lineages persisted in the tropics. Both vicariance and dispersal patterns are detected. Species from Neotropical and south temperate regions are largely derived from immigrant ancestors from north temperate or Palaeotropical regions. Transitions to conifer hosts occurred later, probably during the Palaeogene.</div>
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<fA08 i1="01" i2="1" l="ENG"><s1>Out of the Palaeotropics? Historical biogeography and diversification of the cosmopolitan ectomycorrhizal mushroom family Inocybaceae</s1>
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<fA11 i1="01" i2="1"><s1>BRANDON MATHENY (P.)</s1>
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<fA11 i1="02" i2="1"><s1>AIME (M. Catherine)</s1>
</fA11>
<fA11 i1="03" i2="1"><s1>BOUGHER (Neale L.)</s1>
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<fA11 i1="04" i2="1"><s1>BUYCK (Bart)</s1>
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<fA11 i1="05" i2="1"><s1>DESJARDIN (Dennis E.)</s1>
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<fA11 i1="06" i2="1"><s1>HORAK (Egon)</s1>
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<fA11 i1="07" i2="1"><s1>KROPP (Bradley R.)</s1>
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<fA11 i1="08" i2="1"><s1>LODGE (D. Jean)</s1>
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<fA11 i1="09" i2="1"><s1>SOYTONG (Kasem)</s1>
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<fA11 i1="10" i2="1"><s1>TRAPPE (James M.)</s1>
</fA11>
<fA11 i1="11" i2="1"><s1>HIBBETT (David S.)</s1>
</fA11>
<fA14 i1="01"><s1>Biology Department, Clark University</s1>
<s2>Worcester, MA</s2>
<s3>USA</s3>
<sZ>1 aut.</sZ>
<sZ>11 aut.</sZ>
</fA14>
<fA14 i1="02"><s1>Department of Plant Pathology and Crop Physiology, Louisiana State University Agricultural Center</s1>
<s2>Baton Rouge, LA</s2>
<s3>USA</s3>
<sZ>2 aut.</sZ>
</fA14>
<fA14 i1="03"><s1>Department of Environment and Conservation, Western Australian Herbarium, Bentley Delivery Centre</s1>
<s2>Perth, WA</s2>
<s3>AUS</s3>
<sZ>3 aut.</sZ>
</fA14>
<fA14 i1="04"><s1>Muséum National d'Histoire Naturelle, Département Systématique et Evolution, USM 602 -CP 39</s1>
<s2>Paris</s2>
<s3>FRA</s3>
<sZ>4 aut.</sZ>
</fA14>
<fA14 i1="05"><s1>Department of Biology, San Francisco State University</s1>
<s2>San Francisco, CA</s2>
<s3>USA</s3>
<sZ>5 aut.</sZ>
</fA14>
<fA14 i1="06"><s1>Nikodemweg 5</s1>
<s2>Innsbruck</s2>
<s3>AUT</s3>
<sZ>6 aut.</sZ>
</fA14>
<fA14 i1="07"><s1>Department of Biology, Utah State University</s1>
<s2>Logan, UT</s2>
<s3>USA</s3>
<sZ>7 aut.</sZ>
</fA14>
<fA14 i1="08"><s1>Center for Forest Mycology Research, US Department of Agriculture, Forest Service, Northern Research Station</s1>
<s2>Luquillo</s2>
<s3>PRI</s3>
<sZ>8 aut.</sZ>
</fA14>
<fA14 i1="09"><s1>Faculty of Agricultural Technology, King Mongkut's Institute of Technology Ladkrabang</s1>
<s2>Bangkok</s2>
<s3>THA</s3>
<sZ>9 aut.</sZ>
</fA14>
<fA14 i1="10"><s1>Department of Forest Science, Oregon State University</s1>
<s2>Corvallis, OR</s2>
<s3>USA</s3>
<sZ>10 aut.</sZ>
</fA14>
<fA20><s1>577-592</s1>
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<fA21><s1>2009</s1>
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<fC01 i1="01" l="ENG"><s0>Aim The ectomycorrhizal (ECM) mushroom family Inocybaceae is widespread in north temperate regions, but more than 150 species are encountered in the tropics and the Southern Hemisphere. The relative roles of recent and ancient biogeographical processes, relationships with plant hosts, and the timing of divergences that have shaped the current geographic distribution of the family are investigated. Location Africa, Australia, Neotropics, New Zealand, north temperate zone, Palaeotropics, Southeast Asia, South America, south temperate zone. Methods We reconstruct a phylogeny of the Inocybaceae with a geological timeline using a relaxed molecular clock. Divergence dates of lineages are estimated statistically to test vicariance-based hypotheses concerning relatedness of disjunct ECM taxa. A series of internal maximum time constraints is used to evaluate two different calibrations. Ancestral state reconstruction is used to infer ancestral areas and ancestral plant partners of the family. Results The Palaeotropics are unique in containing representatives of all major clades of Inocybaceae. Six of the seven major clades diversified initially during the Cretaceous, with subsequent radiations probably during the early Palaeogene. Vicariance patterns cannot be rejected that involve area relationships for Africa-Australia, Africa-India and southern South America-Australia. Northern and southern South America, Australia and New Zealand are primarily the recipients of immigrant taxa during the Palaeogene or later. Angiosperms were the earliest hosts of Inocybaceae. Transitions to conifers probably occurred no earlier than 65 Ma. Main conclusions The Inocybaceae initially diversified no later than the Cretaceous in Palaeotropical settings, in association with angiosperms. Diversification within major clades of the family accelerated during the Palaeogene in north and south temperate regions, whereas several relictual lineages persisted in the tropics. Both vicariance and dispersal patterns are detected. Species from Neotropical and south temperate regions are largely derived from immigrant ancestors from north temperate or Palaeotropical regions. Transitions to conifer hosts occurred later, probably during the Palaeogene.</s0>
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<fC03 i1="03" i2="X" l="SPA"><s0>Diversificación</s0>
<s5>03</s5>
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<fC03 i1="04" i2="X" l="FRE"><s0>Dispersion</s0>
<s5>04</s5>
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<fC03 i1="04" i2="X" l="ENG"><s0>Dispersion</s0>
<s5>04</s5>
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<s5>05</s5>
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<fC03 i1="05" i2="X" l="SPA"><s0>Ectomicorriza</s0>
<s5>05</s5>
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<s5>06</s5>
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<s5>06</s5>
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<s5>06</s5>
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<fC03 i1="07" i2="X" l="FRE"><s0>Vicariance</s0>
<s5>07</s5>
</fC03>
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<fC07 i1="01" i2="X" l="SPA"><s0>Micorriza</s0>
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<server><NO>PASCAL 09-0163619 INIST</NO>
<ET>Out of the Palaeotropics? Historical biogeography and diversification of the cosmopolitan ectomycorrhizal mushroom family Inocybaceae</ET>
<AU>BRANDON MATHENY (P.); AIME (M. Catherine); BOUGHER (Neale L.); BUYCK (Bart); DESJARDIN (Dennis E.); HORAK (Egon); KROPP (Bradley R.); LODGE (D. Jean); SOYTONG (Kasem); TRAPPE (James M.); HIBBETT (David S.)</AU>
<AF>Biology Department, Clark University/Worcester, MA/Etats-Unis (1 aut., 11 aut.); Department of Plant Pathology and Crop Physiology, Louisiana State University Agricultural Center/Baton Rouge, LA/Etats-Unis (2 aut.); Department of Environment and Conservation, Western Australian Herbarium, Bentley Delivery Centre/Perth, WA/Australie (3 aut.); Muséum National d'Histoire Naturelle, Département Systématique et Evolution, USM 602 -CP 39/Paris/France (4 aut.); Department of Biology, San Francisco State University/San Francisco, CA/Etats-Unis (5 aut.); Nikodemweg 5/Innsbruck/Autriche (6 aut.); Department of Biology, Utah State University/Logan, UT/Etats-Unis (7 aut.); Center for Forest Mycology Research, US Department of Agriculture, Forest Service, Northern Research Station/Luquillo/Porto Rico (8 aut.); Faculty of Agricultural Technology, King Mongkut's Institute of Technology Ladkrabang/Bangkok/Thaïlande (9 aut.); Department of Forest Science, Oregon State University/Corvallis, OR/Etats-Unis (10 aut.)</AF>
<DT>Publication en série; Niveau analytique</DT>
<SO>Journal of biogeography; ISSN 0305-0270; Coden JBIODN; Royaume-Uni; Da. 2009; Vol. 36; No. 4; Pp. 577-592; Bibl. 3 p.1/4</SO>
<LA>Anglais</LA>
<EA>Aim The ectomycorrhizal (ECM) mushroom family Inocybaceae is widespread in north temperate regions, but more than 150 species are encountered in the tropics and the Southern Hemisphere. The relative roles of recent and ancient biogeographical processes, relationships with plant hosts, and the timing of divergences that have shaped the current geographic distribution of the family are investigated. Location Africa, Australia, Neotropics, New Zealand, north temperate zone, Palaeotropics, Southeast Asia, South America, south temperate zone. Methods We reconstruct a phylogeny of the Inocybaceae with a geological timeline using a relaxed molecular clock. Divergence dates of lineages are estimated statistically to test vicariance-based hypotheses concerning relatedness of disjunct ECM taxa. A series of internal maximum time constraints is used to evaluate two different calibrations. Ancestral state reconstruction is used to infer ancestral areas and ancestral plant partners of the family. Results The Palaeotropics are unique in containing representatives of all major clades of Inocybaceae. Six of the seven major clades diversified initially during the Cretaceous, with subsequent radiations probably during the early Palaeogene. Vicariance patterns cannot be rejected that involve area relationships for Africa-Australia, Africa-India and southern South America-Australia. Northern and southern South America, Australia and New Zealand are primarily the recipients of immigrant taxa during the Palaeogene or later. Angiosperms were the earliest hosts of Inocybaceae. Transitions to conifers probably occurred no earlier than 65 Ma. Main conclusions The Inocybaceae initially diversified no later than the Cretaceous in Palaeotropical settings, in association with angiosperms. Diversification within major clades of the family accelerated during the Palaeogene in north and south temperate regions, whereas several relictual lineages persisted in the tropics. Both vicariance and dispersal patterns are detected. Species from Neotropical and south temperate regions are largely derived from immigrant ancestors from north temperate or Palaeotropical regions. Transitions to conifer hosts occurred later, probably during the Palaeogene.</EA>
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<FD>Historique; Biogéographie; Diversification; Dispersion; Ectomycorhize; Horloge moléculaire; Vicariance; Fungi; Basidiomycota</FD>
<FG>Mycorhize; Symbionte</FG>
<ED>Case history; Biogeography; Diversification; Dispersion; Ectomycorrhiza; Molecular clock; Vicariance; Fungi; Basidiomycota</ED>
<EG>Mycorrhiza; Symbiont</EG>
<SD>Estudio histórico; Biogeografía; Diversificación; Dispersión; Ectomicorriza; Reloj molecular; Vicariancia; Fungi; Basidiomycota</SD>
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Out of the Palaeotropics? Historical biogeography and diversification of the cosmopolitan ectomycorrhizal mushroom family Inocybaceae

Out of the Palaeotropics? Historical biogeography and diversification of the cosmopolitan ectomycorrhizal mushroom family Inocybaceae

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