Differences in mycorrhizal communities between Epipactis palustris, E. helleborine and its presumed sister species E. neerlandica
In orchid species that have populations occurring in strongly contrasting habitats, mycorrhizal divergence and other habitat-specific adaptations may lead to the formation of reproductively isolated taxa and ultimately to species formation. However, little is known about the mycorrhizal communities...
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Veröffentlicht in: | Annals of botany 2016-07, Vol.118 (1), p.105-114 |
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description | In orchid species that have populations occurring in strongly contrasting habitats, mycorrhizal divergence and other habitat-specific adaptations may lead to the formation of reproductively isolated taxa and ultimately to species formation. However, little is known about the mycorrhizal communities associated with recently diverged sister taxa that occupy different habitats.
In this study, 454 amplicon pyrosequencing was used to investigate mycorrhizal communities associating with Epipactis helleborine in its typical forest habitat and with its presumed sister species E. neerlandica that almost exclusively occurs in coastal dune habitats. Samples of the phylogenetically more distant E. palustris, which co-occurred with E. neerlandica, were also included to investigate the role of habitat-specific conditions on mycorrhizal communities.
A total of 105 operational taxonomic units (OTUs) of putative orchid mycorrhizal fungi were observed in the three studied species. The majority of these fungi were endophytic fungi of Helotiales and ectomycorrhizal fungi belonging to Thelephoraceae, Sebacinaceae and Inocybaceae. In addition, a large number of other ectomycorrhizal taxa were detected, including Cortinarius, Cenococcum, Tuber, Geopora, Wilcoxina, Meliniomyces, Hebeloma, Tricholoma, Russula and Peziza Mycorrhizal communities differed significantly between the three species, but differences were most pronounced between the forest species (E. helleborine) and the two dune slack species (E. neerlandica and E. palustris).
The results clearly showed that recently diverged orchid species that occupy different habitats were characterized by significantly different mycorrhizal communities and call for more detailed experiments that aim at elucidating the contribution of habitat-specific adaptations in general and mycorrhizal divergence in particular to the process of speciation in orchids. |
doi_str_mv | 10.1093/aob/mcw015 |
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In this study, 454 amplicon pyrosequencing was used to investigate mycorrhizal communities associating with Epipactis helleborine in its typical forest habitat and with its presumed sister species E. neerlandica that almost exclusively occurs in coastal dune habitats. Samples of the phylogenetically more distant E. palustris, which co-occurred with E. neerlandica, were also included to investigate the role of habitat-specific conditions on mycorrhizal communities.
A total of 105 operational taxonomic units (OTUs) of putative orchid mycorrhizal fungi were observed in the three studied species. The majority of these fungi were endophytic fungi of Helotiales and ectomycorrhizal fungi belonging to Thelephoraceae, Sebacinaceae and Inocybaceae. In addition, a large number of other ectomycorrhizal taxa were detected, including Cortinarius, Cenococcum, Tuber, Geopora, Wilcoxina, Meliniomyces, Hebeloma, Tricholoma, Russula and Peziza Mycorrhizal communities differed significantly between the three species, but differences were most pronounced between the forest species (E. helleborine) and the two dune slack species (E. neerlandica and E. palustris).
The results clearly showed that recently diverged orchid species that occupy different habitats were characterized by significantly different mycorrhizal communities and call for more detailed experiments that aim at elucidating the contribution of habitat-specific adaptations in general and mycorrhizal divergence in particular to the process of speciation in orchids.</description><identifier>ISSN: 0305-7364</identifier><identifier>ISSN: 1095-8290</identifier><identifier>EISSN: 1095-8290</identifier><identifier>DOI: 10.1093/aob/mcw015</identifier><identifier>PMID: 26946528</identifier><language>eng</language><publisher>England: Oxford University Press</publisher><subject>Ascomycota ; Basidiomycota ; Belgium ; Biodiversity ; Cenococcum ; Cortinarius ; Ecosystem ; ectomycorrhizae ; endophytes ; Epipactis ; Forests ; Geopora ; habitats ; Hebeloma ; Helotiales ; Inocybaceae ; Mycorrhizae - physiology ; mycorrhizal fungi ; Orchid Biology ; Orchidaceae - microbiology ; PART OF A HIGHLIGHT ON ORCHID BIOLOGY ; Peziza ; Phylogeny ; Russula ; Sebacinaceae ; sequence analysis ; Sequence Analysis, DNA ; Symbiosis ; Thelephoraceae ; Tricholoma ; Tuber (Tuberaceae)</subject><ispartof>Annals of botany, 2016-07, Vol.118 (1), p.105-114</ispartof><rights>The Author 2016</rights><rights>The Author 2016. Published by Oxford University Press on behalf of the Annals of Botany Company. All rights reserved. For Permissions, please email: journals.permissions@oup.com.</rights><rights>The Author 2016. Published by Oxford University Press on behalf of the Annals of Botany Company. All rights reserved. For Permissions, please email: journals.permissions@oup.com 2016</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c397t-b991e77138c20ca5879757571f37580ae6aaae8cd10d2188b3cafceff37c45473</citedby><cites>FETCH-LOGICAL-c397t-b991e77138c20ca5879757571f37580ae6aaae8cd10d2188b3cafceff37c45473</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.jstor.org/stable/pdf/26526502$$EPDF$$P50$$Gjstor$$H</linktopdf><linktohtml>$$Uhttps://www.jstor.org/stable/26526502$$EHTML$$P50$$Gjstor$$H</linktohtml><link.rule.ids>230,314,723,776,780,799,881,27901,27902,53766,53768,57992,58225</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26946528$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Jacquemyn, Hans</creatorcontrib><creatorcontrib>Waud, Michael</creatorcontrib><creatorcontrib>Lievens, Bart</creatorcontrib><creatorcontrib>Brys, Rein</creatorcontrib><title>Differences in mycorrhizal communities between Epipactis palustris, E. helleborine and its presumed sister species E. neerlandica</title><title>Annals of botany</title><addtitle>Ann Bot</addtitle><description>In orchid species that have populations occurring in strongly contrasting habitats, mycorrhizal divergence and other habitat-specific adaptations may lead to the formation of reproductively isolated taxa and ultimately to species formation. However, little is known about the mycorrhizal communities associated with recently diverged sister taxa that occupy different habitats.
In this study, 454 amplicon pyrosequencing was used to investigate mycorrhizal communities associating with Epipactis helleborine in its typical forest habitat and with its presumed sister species E. neerlandica that almost exclusively occurs in coastal dune habitats. Samples of the phylogenetically more distant E. palustris, which co-occurred with E. neerlandica, were also included to investigate the role of habitat-specific conditions on mycorrhizal communities.
A total of 105 operational taxonomic units (OTUs) of putative orchid mycorrhizal fungi were observed in the three studied species. The majority of these fungi were endophytic fungi of Helotiales and ectomycorrhizal fungi belonging to Thelephoraceae, Sebacinaceae and Inocybaceae. In addition, a large number of other ectomycorrhizal taxa were detected, including Cortinarius, Cenococcum, Tuber, Geopora, Wilcoxina, Meliniomyces, Hebeloma, Tricholoma, Russula and Peziza Mycorrhizal communities differed significantly between the three species, but differences were most pronounced between the forest species (E. helleborine) and the two dune slack species (E. neerlandica and E. palustris).
The results clearly showed that recently diverged orchid species that occupy different habitats were characterized by significantly different mycorrhizal communities and call for more detailed experiments that aim at elucidating the contribution of habitat-specific adaptations in general and mycorrhizal divergence in particular to the process of speciation in orchids.</description><subject>Ascomycota</subject><subject>Basidiomycota</subject><subject>Belgium</subject><subject>Biodiversity</subject><subject>Cenococcum</subject><subject>Cortinarius</subject><subject>Ecosystem</subject><subject>ectomycorrhizae</subject><subject>endophytes</subject><subject>Epipactis</subject><subject>Forests</subject><subject>Geopora</subject><subject>habitats</subject><subject>Hebeloma</subject><subject>Helotiales</subject><subject>Inocybaceae</subject><subject>Mycorrhizae - physiology</subject><subject>mycorrhizal fungi</subject><subject>Orchid Biology</subject><subject>Orchidaceae - microbiology</subject><subject>PART OF A HIGHLIGHT ON ORCHID BIOLOGY</subject><subject>Peziza</subject><subject>Phylogeny</subject><subject>Russula</subject><subject>Sebacinaceae</subject><subject>sequence analysis</subject><subject>Sequence Analysis, DNA</subject><subject>Symbiosis</subject><subject>Thelephoraceae</subject><subject>Tricholoma</subject><subject>Tuber (Tuberaceae)</subject><issn>0305-7364</issn><issn>1095-8290</issn><issn>1095-8290</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkc1LHTEUxUOx1Kd2072SZZGO5mMySTaFYl8_QOimrkMm705fZCYZk0zF7vqfG3lWdFXu4sI9Pw7nchB6R8kZJZqf29ifT-6WUPEKrepFNIppsodWhBPRSN61--gg52tCCOs0fYP262o7wdQK_f3shwESBAcZ-4CnOxdT2vo_dsQuTtMSfPFV6qHcAgS8nv1sXfEZz3Zcckk-f8DrM7yFcYQ-Jh8A27DBvlQiQV4m2ODsc4GE8wzuwaviASCNlfPOHqHXgx0zvH3ch-jqy_rnxbfm8sfX7xefLhvHtSxNrzUFKSlXjhFnhZJaijp04FIoYqGz1oJyG0o2jCrVc2cHB0OVXStayQ_Rx53vvPQ1lINQkh3NnPxk052J1puXSvBb8yv-Nq3mLde0Grx_NEjxZoFczOSzq3_bAHHJhnEqWEckbf-LUkWY5KKjqqKnO9SlmHOC4SkRJeahXlPrNbt6K3zy_Icn9F-fFTjeAde5xPRMr8kEYfwePD2uYQ</recordid><startdate>20160701</startdate><enddate>20160701</enddate><creator>Jacquemyn, Hans</creator><creator>Waud, Michael</creator><creator>Lievens, Bart</creator><creator>Brys, Rein</creator><general>Oxford University Press</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>7S9</scope><scope>L.6</scope><scope>5PM</scope></search><sort><creationdate>20160701</creationdate><title>Differences in mycorrhizal communities between Epipactis palustris, E. helleborine and its presumed sister species E. neerlandica</title><author>Jacquemyn, Hans ; Waud, Michael ; Lievens, Bart ; Brys, Rein</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c397t-b991e77138c20ca5879757571f37580ae6aaae8cd10d2188b3cafceff37c45473</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Ascomycota</topic><topic>Basidiomycota</topic><topic>Belgium</topic><topic>Biodiversity</topic><topic>Cenococcum</topic><topic>Cortinarius</topic><topic>Ecosystem</topic><topic>ectomycorrhizae</topic><topic>endophytes</topic><topic>Epipactis</topic><topic>Forests</topic><topic>Geopora</topic><topic>habitats</topic><topic>Hebeloma</topic><topic>Helotiales</topic><topic>Inocybaceae</topic><topic>Mycorrhizae - physiology</topic><topic>mycorrhizal fungi</topic><topic>Orchid Biology</topic><topic>Orchidaceae - microbiology</topic><topic>PART OF A HIGHLIGHT ON ORCHID BIOLOGY</topic><topic>Peziza</topic><topic>Phylogeny</topic><topic>Russula</topic><topic>Sebacinaceae</topic><topic>sequence analysis</topic><topic>Sequence Analysis, DNA</topic><topic>Symbiosis</topic><topic>Thelephoraceae</topic><topic>Tricholoma</topic><topic>Tuber (Tuberaceae)</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Jacquemyn, Hans</creatorcontrib><creatorcontrib>Waud, Michael</creatorcontrib><creatorcontrib>Lievens, Bart</creatorcontrib><creatorcontrib>Brys, Rein</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>AGRICOLA</collection><collection>AGRICOLA - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Annals of botany</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Jacquemyn, Hans</au><au>Waud, Michael</au><au>Lievens, Bart</au><au>Brys, Rein</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Differences in mycorrhizal communities between Epipactis palustris, E. helleborine and its presumed sister species E. neerlandica</atitle><jtitle>Annals of botany</jtitle><addtitle>Ann Bot</addtitle><date>2016-07-01</date><risdate>2016</risdate><volume>118</volume><issue>1</issue><spage>105</spage><epage>114</epage><pages>105-114</pages><issn>0305-7364</issn><issn>1095-8290</issn><eissn>1095-8290</eissn><abstract>In orchid species that have populations occurring in strongly contrasting habitats, mycorrhizal divergence and other habitat-specific adaptations may lead to the formation of reproductively isolated taxa and ultimately to species formation. However, little is known about the mycorrhizal communities associated with recently diverged sister taxa that occupy different habitats.
In this study, 454 amplicon pyrosequencing was used to investigate mycorrhizal communities associating with Epipactis helleborine in its typical forest habitat and with its presumed sister species E. neerlandica that almost exclusively occurs in coastal dune habitats. Samples of the phylogenetically more distant E. palustris, which co-occurred with E. neerlandica, were also included to investigate the role of habitat-specific conditions on mycorrhizal communities.
A total of 105 operational taxonomic units (OTUs) of putative orchid mycorrhizal fungi were observed in the three studied species. The majority of these fungi were endophytic fungi of Helotiales and ectomycorrhizal fungi belonging to Thelephoraceae, Sebacinaceae and Inocybaceae. In addition, a large number of other ectomycorrhizal taxa were detected, including Cortinarius, Cenococcum, Tuber, Geopora, Wilcoxina, Meliniomyces, Hebeloma, Tricholoma, Russula and Peziza Mycorrhizal communities differed significantly between the three species, but differences were most pronounced between the forest species (E. helleborine) and the two dune slack species (E. neerlandica and E. palustris).
The results clearly showed that recently diverged orchid species that occupy different habitats were characterized by significantly different mycorrhizal communities and call for more detailed experiments that aim at elucidating the contribution of habitat-specific adaptations in general and mycorrhizal divergence in particular to the process of speciation in orchids.</abstract><cop>England</cop><pub>Oxford University Press</pub><pmid>26946528</pmid><doi>10.1093/aob/mcw015</doi><tpages>10</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Ascomycota Basidiomycota Belgium Biodiversity Cenococcum Cortinarius Ecosystem ectomycorrhizae endophytes Epipactis Forests Geopora habitats Hebeloma Helotiales Inocybaceae Mycorrhizae - physiology mycorrhizal fungi Orchid Biology Orchidaceae - microbiology PART OF A HIGHLIGHT ON ORCHID BIOLOGY Peziza Phylogeny Russula Sebacinaceae sequence analysis Sequence Analysis, DNA Symbiosis Thelephoraceae Tricholoma Tuber (Tuberaceae) |
title | Differences in mycorrhizal communities between Epipactis palustris, E. helleborine and its presumed sister species E. neerlandica |
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