Ectomycorrhizas associated with a relict population of Dryas octopetala in the Burren, western Ireland. I. Distribution of ectomycorrhizas in relation to vegetation and soil characteristics
The distribution of ectomycorrhizas on Dryas octopetala L in grass heaths of the 450 km2 karst region known as the Burren in Western Ireland was examined in relation to soil factors and vegetation type. Ectomycorrhizas were identified or characterised from 56 soil cores from 30 sites, and the occurr...
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description | The distribution of ectomycorrhizas on Dryas octopetala L in grass heaths of the 450 km2 karst region known as the Burren in Western Ireland was examined in relation to soil factors and vegetation type. Ectomycorrhizas were identified or characterised from 56 soil cores from 30 sites, and the occurrence of each ectomycorrhizal (EM) type was quantified by estimating the total length of mycorrhizal tips of each type. Soil organic matter, total nitrogen, extractable phosphorus, pH and depth were the soil factors determined. In total, 24 EM types were recorded. The EM community of Dryas roots was significantly more species-rich in one vegetation type--Hyperico-Dryadetum--than in others (Arctostaphylo-Dryadetum or Asperulo-Seslerietum). Multiple linear regression analyses indicated that soil organic matter and soil depth explained a significant portion of the variation in EM abundance, while soil organic matter and extractable phosphorus explained a significant portion of the variation in EM diversity. Canonical correspondence analysis showed that some individual EM types (e.g. Craterellus lutescens, Cenococcum geophilum, Tomentella sp., Boletus sp.) exhibited distinct soil preferences, most markedly in relation to soil organic matter, which, in this analysis, was the main significant soil variable distinguishing the three vegetation types. |
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The EM community of Dryas roots was significantly more species-rich in one vegetation type--Hyperico-Dryadetum--than in others (Arctostaphylo-Dryadetum or Asperulo-Seslerietum). Multiple linear regression analyses indicated that soil organic matter and soil depth explained a significant portion of the variation in EM abundance, while soil organic matter and extractable phosphorus explained a significant portion of the variation in EM diversity. Canonical correspondence analysis showed that some individual EM types (e.g. Craterellus lutescens, Cenococcum geophilum, Tomentella sp., Boletus sp.) exhibited distinct soil preferences, most markedly in relation to soil organic matter, which, in this analysis, was the main significant soil variable distinguishing the three vegetation types.</description><identifier>ISSN: 0940-6360</identifier><identifier>EISSN: 1432-1890</identifier><identifier>DOI: 10.1007/s00572-005-0347-4</identifier><identifier>PMID: 15726435</identifier><language>eng</language><publisher>Berlin: Springer</publisher><subject>Ascomycota - isolation & purification ; Basidiomycota - isolation & purification ; Biodiversity ; Biological and medical sciences ; Dryas ; ectomycorrhizae ; edaphic factors ; Fundamental and applied biological sciences. 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I. Distribution of ectomycorrhizas in relation to vegetation and soil characteristics</title><title>Mycorrhiza</title><addtitle>Mycorrhiza</addtitle><description>The distribution of ectomycorrhizas on Dryas octopetala L in grass heaths of the 450 km2 karst region known as the Burren in Western Ireland was examined in relation to soil factors and vegetation type. Ectomycorrhizas were identified or characterised from 56 soil cores from 30 sites, and the occurrence of each ectomycorrhizal (EM) type was quantified by estimating the total length of mycorrhizal tips of each type. Soil organic matter, total nitrogen, extractable phosphorus, pH and depth were the soil factors determined. In total, 24 EM types were recorded. The EM community of Dryas roots was significantly more species-rich in one vegetation type--Hyperico-Dryadetum--than in others (Arctostaphylo-Dryadetum or Asperulo-Seslerietum). Multiple linear regression analyses indicated that soil organic matter and soil depth explained a significant portion of the variation in EM abundance, while soil organic matter and extractable phosphorus explained a significant portion of the variation in EM diversity. Canonical correspondence analysis showed that some individual EM types (e.g. Craterellus lutescens, Cenococcum geophilum, Tomentella sp., Boletus sp.) exhibited distinct soil preferences, most markedly in relation to soil organic matter, which, in this analysis, was the main significant soil variable distinguishing the three vegetation types.</description><subject>Ascomycota - isolation & purification</subject><subject>Basidiomycota - isolation & purification</subject><subject>Biodiversity</subject><subject>Biological and medical sciences</subject><subject>Dryas</subject><subject>ectomycorrhizae</subject><subject>edaphic factors</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Hydrogen-Ion Concentration</subject><subject>Ireland</subject><subject>Karst</subject><subject>Linear Models</subject><subject>Mycorrhizae - classification</subject><subject>Mycorrhizae - isolation & purification</subject><subject>mycorrhizal fungi</subject><subject>Nitrogen - analysis</subject><subject>Organic Chemicals - analysis</subject><subject>Organic matter</subject><subject>Organic phosphorus</subject><subject>Parasitism and symbiosis</subject><subject>Phosphorus - analysis</subject><subject>plant communities</subject><subject>Plant physiology and development</subject><subject>Plant Roots - microbiology</subject><subject>roots</subject><subject>Rosaceae - microbiology</subject><subject>Soil - analysis</subject><subject>soil chemistry</subject><subject>Soil depth</subject><subject>Soil organic matter</subject><subject>Soils</subject><subject>species diversity</subject><subject>Statistics as Topic</subject><subject>Symbiosis</subject><subject>Vegetation</subject><issn>0940-6360</issn><issn>1432-1890</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2005</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>BENPR</sourceid><recordid>eNqFks1u1DAQgC0EokvhAbiAhQQnsozjv-QIbYGVKnGAni3H63RdZeNgO1TLu_FuzHYXVeqFiy3b33z2jIeQlwyWDEB_yABS1xWOFXChK_GILJjgdcWaFh6TBbQCKsUVnJBnOd8AMK04e0pOGIYpweWC_LlwJW53Lqa0Cb9tpjbn6IItfk1vQ9lQS5Mfgit0itM82BLiSGNPz9MO4YjBky92sDSMtGw8_TSn5Mf39Nbn4tNIVxhtx_WSrpb0POSSQjf_c_gHV6NiT98dl0h_-WtU363QQHMMA3Ubm6xDM6qCy8_Jk94O2b84zqfk6vPFj7Ov1eW3L6uzj5eVE4yVSkheNxa4XOuOOdvw2nHJWuW8E71qRYel6LXuoNdOCsAd1oi2U6qzogbl-Cl5d_BOKf6cMTWzDdn5AVPzcc5GNRKr3NT_BfEDsPRCIPjmAXgT5zRiEkYxDrWUIBFiB8ilmHPyvZlS2Nq0MwzMvgPMoQMMjmbfAWYvfnUUz93Wr-8jjl-OwNsjYLOzQ5_s6EK-5zRo3TaA3OsD19to7DVW3Fx9rwEfx0DVrQb-FxHMxNw</recordid><startdate>20050901</startdate><enddate>20050901</enddate><creator>Harrington, T.J</creator><creator>Mitchell, D.T</creator><general>Springer</general><general>Springer Nature B.V</general><scope>FBQ</scope><scope>IQODW</scope><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>3V.</scope><scope>7T7</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8FD</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AEUYN</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>C1K</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M7N</scope><scope>M7P</scope><scope>P64</scope><scope>PHGZM</scope><scope>PHGZT</scope><scope>PJZUB</scope><scope>PKEHL</scope><scope>PPXIY</scope><scope>PQEST</scope><scope>PQGLB</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>7X8</scope></search><sort><creationdate>20050901</creationdate><title>Ectomycorrhizas associated with a relict population of Dryas octopetala in the Burren, western Ireland. I. Distribution of ectomycorrhizas in relation to vegetation and soil characteristics</title><author>Harrington, T.J ; Mitchell, D.T</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c411t-45328a035d7b1ca832c35196cec4f694b435f77b0f7c5406941849b66ba4206c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2005</creationdate><topic>Ascomycota - isolation & purification</topic><topic>Basidiomycota - isolation & purification</topic><topic>Biodiversity</topic><topic>Biological and medical sciences</topic><topic>Dryas</topic><topic>ectomycorrhizae</topic><topic>edaphic factors</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Hydrogen-Ion Concentration</topic><topic>Ireland</topic><topic>Karst</topic><topic>Linear Models</topic><topic>Mycorrhizae - classification</topic><topic>Mycorrhizae - isolation & purification</topic><topic>mycorrhizal fungi</topic><topic>Nitrogen - analysis</topic><topic>Organic Chemicals - analysis</topic><topic>Organic matter</topic><topic>Organic phosphorus</topic><topic>Parasitism and symbiosis</topic><topic>Phosphorus - analysis</topic><topic>plant communities</topic><topic>Plant physiology and development</topic><topic>Plant Roots - microbiology</topic><topic>roots</topic><topic>Rosaceae - microbiology</topic><topic>Soil - analysis</topic><topic>soil chemistry</topic><topic>Soil depth</topic><topic>Soil organic matter</topic><topic>Soils</topic><topic>species diversity</topic><topic>Statistics as Topic</topic><topic>Symbiosis</topic><topic>Vegetation</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Harrington, T.J</creatorcontrib><creatorcontrib>Mitchell, D.T</creatorcontrib><collection>AGRIS</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest One Sustainability</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biological Science Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>ProQuest Central (New)</collection><collection>ProQuest One Academic (New)</collection><collection>ProQuest Health & Medical Research Collection</collection><collection>ProQuest One Academic Middle East (New)</collection><collection>ProQuest One Health & Nursing</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Applied & Life Sciences</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>MEDLINE - Academic</collection><jtitle>Mycorrhiza</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Harrington, T.J</au><au>Mitchell, D.T</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Ectomycorrhizas associated with a relict population of Dryas octopetala in the Burren, western Ireland. I. Distribution of ectomycorrhizas in relation to vegetation and soil characteristics</atitle><jtitle>Mycorrhiza</jtitle><addtitle>Mycorrhiza</addtitle><date>2005-09-01</date><risdate>2005</risdate><volume>15</volume><issue>6</issue><spage>425</spage><epage>433</epage><pages>425-433</pages><issn>0940-6360</issn><eissn>1432-1890</eissn><abstract>The distribution of ectomycorrhizas on Dryas octopetala L in grass heaths of the 450 km2 karst region known as the Burren in Western Ireland was examined in relation to soil factors and vegetation type. Ectomycorrhizas were identified or characterised from 56 soil cores from 30 sites, and the occurrence of each ectomycorrhizal (EM) type was quantified by estimating the total length of mycorrhizal tips of each type. Soil organic matter, total nitrogen, extractable phosphorus, pH and depth were the soil factors determined. In total, 24 EM types were recorded. The EM community of Dryas roots was significantly more species-rich in one vegetation type--Hyperico-Dryadetum--than in others (Arctostaphylo-Dryadetum or Asperulo-Seslerietum). Multiple linear regression analyses indicated that soil organic matter and soil depth explained a significant portion of the variation in EM abundance, while soil organic matter and extractable phosphorus explained a significant portion of the variation in EM diversity. Canonical correspondence analysis showed that some individual EM types (e.g. Craterellus lutescens, Cenococcum geophilum, Tomentella sp., Boletus sp.) exhibited distinct soil preferences, most markedly in relation to soil organic matter, which, in this analysis, was the main significant soil variable distinguishing the three vegetation types.</abstract><cop>Berlin</cop><pub>Springer</pub><pmid>15726435</pmid><doi>10.1007/s00572-005-0347-4</doi><tpages>9</tpages></addata></record> |
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subjects | Ascomycota - isolation & purification Basidiomycota - isolation & purification Biodiversity Biological and medical sciences Dryas ectomycorrhizae edaphic factors Fundamental and applied biological sciences. Psychology Hydrogen-Ion Concentration Ireland Karst Linear Models Mycorrhizae - classification Mycorrhizae - isolation & purification mycorrhizal fungi Nitrogen - analysis Organic Chemicals - analysis Organic matter Organic phosphorus Parasitism and symbiosis Phosphorus - analysis plant communities Plant physiology and development Plant Roots - microbiology roots Rosaceae - microbiology Soil - analysis soil chemistry Soil depth Soil organic matter Soils species diversity Statistics as Topic Symbiosis Vegetation |
title | Ectomycorrhizas associated with a relict population of Dryas octopetala in the Burren, western Ireland. I. Distribution of ectomycorrhizas in relation to vegetation and soil characteristics |
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