Arbuscular mycorrhiza enhance the rate of litter decomposition while inhibiting soil microbial community development.
Identifieur interne : 000D67 ( Main/Corpus ); précédent : 000D66; suivant : 000D68Arbuscular mycorrhiza enhance the rate of litter decomposition while inhibiting soil microbial community development.
Auteurs : Heng Gui ; Kevin Hyde ; Jianchu Xu ; Peter MortimerSource :
- Scientific reports [ 2045-2322 ] ; 2017.
English descriptors
- KwdEn :
- Biodegradation, Environmental (MeSH), Calophyllum (microbiology), Composting (MeSH), Fatty Acids (analysis), Fatty Acids (biosynthesis), Glomeromycota (growth & development), Glomeromycota (metabolism), Kinetics (MeSH), Microbial Consortia (physiology), Mycorrhizae (growth & development), Mycorrhizae (metabolism), Nitrogen (analysis), Nitrogen (metabolism), Phospholipids (analysis), Phospholipids (biosynthesis), Plant Leaves (chemistry), Plant Leaves (metabolism), Plant Leaves (microbiology), Soil (chemistry), Soil Microbiology (MeSH).
- MESH :
- chemical , analysis : Fatty Acids, Nitrogen, Phospholipids.
- chemical , biosynthesis : Fatty Acids, Phospholipids.
- chemistry : Plant Leaves, Soil.
- growth & development : Glomeromycota, Mycorrhizae.
- metabolism : Glomeromycota, Mycorrhizae, Nitrogen, Plant Leaves.
- microbiology : Calophyllum, Plant Leaves.
- physiology : Microbial Consortia.
- Biodegradation, Environmental, Composting, Kinetics, Soil Microbiology.
Abstract
Although there is a growing amount of evidence that arbuscular mycorrhizal fungi (AMF) influence the decomposition process, the extent of their involvement remains unclear. Therefore, given this knowledge gap, our aim was to test how AMF influence the soil decomposer communities. Dual compartment microcosms, where AMF (Glomus mosseae) were either allowed access (AM+) to or excluded (AM-) from forest soil compartments containing litterbags (leaf litter from Calophyllum polyanthum) were used. The experiment ran for six months, with destructive harvests at 0, 90, 120, 150, and 180 days. For each harvest we measured AMF colonization, soil nutrients, litter mass loss, and microbial biomass (using phospholipid fatty acid analysis (PLFA)). AMF significantly enhanced litter decomposition in the first 5 months, whilst delaying the development of total microbial biomass (represented by total PLFA) from T150 to T180. A significant decline in soil available N was observed through the course of the experiment for both treatments. This study shows that AMF have the capacity to interact with soil microbial communities and inhibit the development of fungal and bacterial groups in the soil at the later stage of the litter decomposition (180 days), whilst enhancing the rates of decomposition.
DOI: 10.1038/srep42184
PubMed: 28176855
PubMed Central: PMC5296878
Links to Exploration step
pubmed:28176855Le document en format XML
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uniqKey="Hyde K" first="Kevin" last="Hyde">Kevin Hyde</name><affiliation><nlm:affiliation>Key laboratory for Plant Diversity and Biogeography of East Asia, Kunming Institute of Botany, Chinese Academy of Sciences, Kunming 650201, China.</nlm:affiliation></affiliation><affiliation><nlm:affiliation>Centre of Excellence in Fungal Research, Mae Fah Luang University, Chiang Rai 57100, Thailand.</nlm:affiliation></affiliation><affiliation><nlm:affiliation>School of Science, Mae Fah Luang University, Chiang Rai 57100, Thailand.</nlm:affiliation></affiliation></author><author><name sortKey="Xu, Jianchu" sort="Xu, Jianchu" uniqKey="Xu J" first="Jianchu" last="Xu">Jianchu Xu</name><affiliation><nlm:affiliation>Key laboratory for Plant Diversity and Biogeography of East Asia, Kunming Institute of Botany, Chinese Academy of Sciences, Kunming 650201, China.</nlm:affiliation></affiliation><affiliation><nlm:affiliation>World Agroforestry Centre, East and Central Asia, Kunming 650201, China.</nlm:affiliation></affiliation></author><author><name sortKey="Mortimer, Peter" sort="Mortimer, Peter" uniqKey="Mortimer P" first="Peter" last="Mortimer">Peter Mortimer</name><affiliation><nlm:affiliation>Key laboratory for Plant Diversity and Biogeography of East Asia, Kunming Institute of Botany, Chinese Academy of Sciences, Kunming 650201, China.</nlm:affiliation></affiliation><affiliation><nlm:affiliation>World Agroforestry Centre, East and Central Asia, Kunming 650201, China.</nlm:affiliation></affiliation></author></titleStmt><publicationStmt><idno type="wicri:source">PubMed</idno><date when="2017">2017</date><idno type="RBID">pubmed:28176855</idno><idno type="pmid">28176855</idno><idno type="doi">10.1038/srep42184</idno><idno type="pmc">PMC5296878</idno><idno type="wicri:Area/Main/Corpus">000D67</idno><idno type="wicri:explorRef" wicri:stream="Main" wicri:step="Corpus" wicri:corpus="PubMed">000D67</idno></publicationStmt><sourceDesc><biblStruct><analytic><title xml:lang="en">Arbuscular mycorrhiza enhance the rate of litter decomposition while inhibiting soil microbial community development.</title><author><name sortKey="Gui, Heng" sort="Gui, Heng" uniqKey="Gui H" first="Heng" last="Gui">Heng Gui</name><affiliation><nlm:affiliation>Key laboratory for Plant Diversity and Biogeography of East Asia, Kunming Institute of Botany, Chinese Academy of Sciences, Kunming 650201, China.</nlm:affiliation></affiliation><affiliation><nlm:affiliation>World Agroforestry Centre, East and Central Asia, Kunming 650201, China.</nlm:affiliation></affiliation><affiliation><nlm:affiliation>Centre of Excellence in Fungal Research, Mae Fah Luang University, Chiang Rai 57100, Thailand.</nlm:affiliation></affiliation><affiliation><nlm:affiliation>School of Science, Mae Fah Luang University, Chiang Rai 57100, Thailand.</nlm:affiliation></affiliation></author><author><name sortKey="Hyde, Kevin" sort="Hyde, Kevin" uniqKey="Hyde K" first="Kevin" last="Hyde">Kevin Hyde</name><affiliation><nlm:affiliation>Key laboratory for Plant Diversity and Biogeography of East Asia, Kunming Institute of Botany, Chinese Academy of Sciences, Kunming 650201, China.</nlm:affiliation></affiliation><affiliation><nlm:affiliation>Centre of Excellence in Fungal Research, Mae Fah Luang University, Chiang Rai 57100, Thailand.</nlm:affiliation></affiliation><affiliation><nlm:affiliation>School of Science, Mae Fah Luang University, Chiang Rai 57100, Thailand.</nlm:affiliation></affiliation></author><author><name sortKey="Xu, Jianchu" sort="Xu, Jianchu" uniqKey="Xu J" first="Jianchu" last="Xu">Jianchu Xu</name><affiliation><nlm:affiliation>Key laboratory for Plant Diversity and Biogeography of East Asia, Kunming Institute of Botany, Chinese Academy of Sciences, Kunming 650201, China.</nlm:affiliation></affiliation><affiliation><nlm:affiliation>World Agroforestry Centre, East and Central Asia, Kunming 650201, China.</nlm:affiliation></affiliation></author><author><name sortKey="Mortimer, Peter" sort="Mortimer, Peter" uniqKey="Mortimer P" first="Peter" last="Mortimer">Peter Mortimer</name><affiliation><nlm:affiliation>Key laboratory for Plant Diversity and Biogeography of East Asia, Kunming Institute of Botany, Chinese Academy of Sciences, Kunming 650201, China.</nlm:affiliation></affiliation><affiliation><nlm:affiliation>World Agroforestry Centre, East and Central Asia, Kunming 650201, China.</nlm:affiliation></affiliation></author></analytic><series><title level="j">Scientific reports</title><idno type="eISSN">2045-2322</idno><imprint><date when="2017" type="published">2017</date></imprint></series></biblStruct></sourceDesc></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Biodegradation, Environmental (MeSH)</term><term>Calophyllum (microbiology)</term><term>Composting (MeSH)</term><term>Fatty Acids (analysis)</term><term>Fatty Acids (biosynthesis)</term><term>Glomeromycota (growth & development)</term><term>Glomeromycota (metabolism)</term><term>Kinetics (MeSH)</term><term>Microbial Consortia (physiology)</term><term>Mycorrhizae (growth & development)</term><term>Mycorrhizae (metabolism)</term><term>Nitrogen (analysis)</term><term>Nitrogen (metabolism)</term><term>Phospholipids (analysis)</term><term>Phospholipids (biosynthesis)</term><term>Plant Leaves (chemistry)</term><term>Plant Leaves (metabolism)</term><term>Plant Leaves (microbiology)</term><term>Soil (chemistry)</term><term>Soil Microbiology (MeSH)</term></keywords><keywords scheme="MESH" type="chemical" qualifier="analysis" xml:lang="en"><term>Fatty Acids</term><term>Nitrogen</term><term>Phospholipids</term></keywords><keywords scheme="MESH" type="chemical" qualifier="biosynthesis" xml:lang="en"><term>Fatty Acids</term><term>Phospholipids</term></keywords><keywords scheme="MESH" qualifier="chemistry" xml:lang="en"><term>Plant Leaves</term><term>Soil</term></keywords><keywords scheme="MESH" qualifier="growth & development" xml:lang="en"><term>Glomeromycota</term><term>Mycorrhizae</term></keywords><keywords scheme="MESH" qualifier="metabolism" xml:lang="en"><term>Glomeromycota</term><term>Mycorrhizae</term><term>Nitrogen</term><term>Plant Leaves</term></keywords><keywords scheme="MESH" qualifier="microbiology" xml:lang="en"><term>Calophyllum</term><term>Plant Leaves</term></keywords><keywords scheme="MESH" qualifier="physiology" xml:lang="en"><term>Microbial Consortia</term></keywords><keywords scheme="MESH" xml:lang="en"><term>Biodegradation, Environmental</term><term>Composting</term><term>Kinetics</term><term>Soil Microbiology</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">Although there is a growing amount of evidence that arbuscular mycorrhizal fungi (AMF) influence the decomposition process, the extent of their involvement remains unclear. Therefore, given this knowledge gap, our aim was to test how AMF influence the soil decomposer communities. Dual compartment microcosms, where AMF (Glomus mosseae) were either allowed access (AM+) to or excluded (AM-) from forest soil compartments containing litterbags (leaf litter from Calophyllum polyanthum) were used. The experiment ran for six months, with destructive harvests at 0, 90, 120, 150, and 180 days. For each harvest we measured AMF colonization, soil nutrients, litter mass loss, and microbial biomass (using phospholipid fatty acid analysis (PLFA)). AMF significantly enhanced litter decomposition in the first 5 months, whilst delaying the development of total microbial biomass (represented by total PLFA) from T<sub>150</sub> to T<sub>180</sub>. A significant decline in soil available N was observed through the course of the experiment for both treatments. This study shows that AMF have the capacity to interact with soil microbial communities and inhibit the development of fungal and bacterial groups in the soil at the later stage of the litter decomposition (180 days), whilst enhancing the rates of decomposition.</div></front></TEI><pubmed><MedlineCitation Status="MEDLINE" Owner="NLM"><PMID Version="1">28176855</PMID><DateCompleted><Year>2018</Year><Month>10</Month><Day>30</Day></DateCompleted><DateRevised><Year>2018</Year><Month>11</Month><Day>13</Day></DateRevised><Article PubModel="Electronic"><Journal><ISSN IssnType="Electronic">2045-2322</ISSN><JournalIssue CitedMedium="Internet"><Volume>7</Volume><PubDate><Year>2017</Year><Month>02</Month><Day>08</Day></PubDate></JournalIssue><Title>Scientific reports</Title><ISOAbbreviation>Sci Rep</ISOAbbreviation></Journal><ArticleTitle>Arbuscular mycorrhiza enhance the rate of litter decomposition while inhibiting soil microbial community development.</ArticleTitle><Pagination><MedlinePgn>42184</MedlinePgn></Pagination><ELocationID EIdType="doi" ValidYN="Y">10.1038/srep42184</ELocationID><Abstract><AbstractText>Although there is a growing amount of evidence that arbuscular mycorrhizal fungi (AMF) influence the decomposition process, the extent of their involvement remains unclear. Therefore, given this knowledge gap, our aim was to test how AMF influence the soil decomposer communities. Dual compartment microcosms, where AMF (Glomus mosseae) were either allowed access (AM+) to or excluded (AM-) from forest soil compartments containing litterbags (leaf litter from Calophyllum polyanthum) were used. The experiment ran for six months, with destructive harvests at 0, 90, 120, 150, and 180 days. For each harvest we measured AMF colonization, soil nutrients, litter mass loss, and microbial biomass (using phospholipid fatty acid analysis (PLFA)). AMF significantly enhanced litter decomposition in the first 5 months, whilst delaying the development of total microbial biomass (represented by total PLFA) from T<sub>150</sub> to T<sub>180</sub>. A significant decline in soil available N was observed through the course of the experiment for both treatments. This study shows that AMF have the capacity to interact with soil microbial communities and inhibit the development of fungal and bacterial groups in the soil at the later stage of the litter decomposition (180 days), whilst enhancing the rates of decomposition.</AbstractText></Abstract><AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Gui</LastName><ForeName>Heng</ForeName><Initials>H</Initials><AffiliationInfo><Affiliation>Key laboratory for Plant Diversity and Biogeography of East Asia, Kunming Institute of Botany, Chinese Academy of Sciences, Kunming 650201, China.</Affiliation></AffiliationInfo><AffiliationInfo><Affiliation>World Agroforestry Centre, East and Central Asia, Kunming 650201, China.</Affiliation></AffiliationInfo><AffiliationInfo><Affiliation>Centre of Excellence in Fungal Research, Mae Fah Luang University, Chiang Rai 57100, Thailand.</Affiliation></AffiliationInfo><AffiliationInfo><Affiliation>School of Science, Mae Fah Luang University, Chiang Rai 57100, Thailand.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Hyde</LastName><ForeName>Kevin</ForeName><Initials>K</Initials><AffiliationInfo><Affiliation>Key laboratory for Plant Diversity and Biogeography of East Asia, Kunming Institute of Botany, Chinese Academy of Sciences, Kunming 650201, China.</Affiliation></AffiliationInfo><AffiliationInfo><Affiliation>Centre of Excellence in Fungal Research, Mae Fah Luang University, Chiang Rai 57100, Thailand.</Affiliation></AffiliationInfo><AffiliationInfo><Affiliation>School of Science, Mae Fah Luang University, Chiang Rai 57100, Thailand.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Xu</LastName><ForeName>Jianchu</ForeName><Initials>J</Initials><AffiliationInfo><Affiliation>Key laboratory for Plant Diversity and Biogeography of East Asia, Kunming Institute of Botany, Chinese Academy of Sciences, Kunming 650201, China.</Affiliation></AffiliationInfo><AffiliationInfo><Affiliation>World Agroforestry Centre, East and Central Asia, Kunming 650201, China.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Mortimer</LastName><ForeName>Peter</ForeName><Initials>P</Initials><AffiliationInfo><Affiliation>Key laboratory for Plant Diversity and Biogeography of East Asia, Kunming Institute of Botany, Chinese Academy of Sciences, Kunming 650201, China.</Affiliation></AffiliationInfo><AffiliationInfo><Affiliation>World Agroforestry Centre, East and Central Asia, Kunming 650201, China.</Affiliation></AffiliationInfo></Author></AuthorList><Language>eng</Language><PublicationTypeList><PublicationType UI="D016428">Journal Article</PublicationType><PublicationType UI="D013485">Research Support, Non-U.S. Gov't</PublicationType></PublicationTypeList><ArticleDate DateType="Electronic"><Year>2017</Year><Month>02</Month><Day>08</Day></ArticleDate></Article><MedlineJournalInfo><Country>England</Country><MedlineTA>Sci Rep</MedlineTA><NlmUniqueID>101563288</NlmUniqueID><ISSNLinking>2045-2322</ISSNLinking></MedlineJournalInfo><ChemicalList><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="D005227">Fatty Acids</NameOfSubstance></Chemical><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="D010743">Phospholipids</NameOfSubstance></Chemical><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="D012987">Soil</NameOfSubstance></Chemical><Chemical><RegistryNumber>N762921K75</RegistryNumber><NameOfSubstance UI="D009584">Nitrogen</NameOfSubstance></Chemical></ChemicalList><CitationSubset>IM</CitationSubset><CommentsCorrectionsList><CommentsCorrections RefType="ErratumIn"><RefSource>Sci Rep. 2017 Apr 28;7:45947</RefSource><PMID Version="1">28452982</PMID></CommentsCorrections></CommentsCorrectionsList><MeshHeadingList><MeshHeading><DescriptorName UI="D001673" MajorTopicYN="N">Biodegradation, Environmental</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D029759" MajorTopicYN="N">Calophyllum</DescriptorName><QualifierName UI="Q000382" MajorTopicYN="N">microbiology</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D000076282" MajorTopicYN="Y">Composting</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D005227" MajorTopicYN="N">Fatty Acids</DescriptorName><QualifierName UI="Q000032" MajorTopicYN="N">analysis</QualifierName><QualifierName UI="Q000096" MajorTopicYN="N">biosynthesis</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D055137" MajorTopicYN="N">Glomeromycota</DescriptorName><QualifierName UI="Q000254" MajorTopicYN="N">growth & development</QualifierName><QualifierName UI="Q000378" MajorTopicYN="Y">metabolism</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D007700" MajorTopicYN="N">Kinetics</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D059013" MajorTopicYN="N">Microbial Consortia</DescriptorName><QualifierName UI="Q000502" MajorTopicYN="N">physiology</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D038821" MajorTopicYN="N">Mycorrhizae</DescriptorName><QualifierName UI="Q000254" MajorTopicYN="N">growth & development</QualifierName><QualifierName UI="Q000378" MajorTopicYN="Y">metabolism</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D009584" MajorTopicYN="N">Nitrogen</DescriptorName><QualifierName UI="Q000032" MajorTopicYN="N">analysis</QualifierName><QualifierName UI="Q000378" MajorTopicYN="N">metabolism</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D010743" MajorTopicYN="N">Phospholipids</DescriptorName><QualifierName UI="Q000032" MajorTopicYN="N">analysis</QualifierName><QualifierName UI="Q000096" MajorTopicYN="N">biosynthesis</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D018515" MajorTopicYN="N">Plant Leaves</DescriptorName><QualifierName UI="Q000737" MajorTopicYN="N">chemistry</QualifierName><QualifierName UI="Q000378" MajorTopicYN="N">metabolism</QualifierName><QualifierName UI="Q000382" MajorTopicYN="Y">microbiology</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D012987" MajorTopicYN="N">Soil</DescriptorName><QualifierName UI="Q000737" MajorTopicYN="N">chemistry</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D012988" MajorTopicYN="Y">Soil Microbiology</DescriptorName></MeshHeading></MeshHeadingList><CoiStatement>The authors declare no competing financial interests.</CoiStatement></MedlineCitation><PubmedData><History><PubMedPubDate PubStatus="received"><Year>2016</Year><Month>08</Month><Day>15</Day></PubMedPubDate><PubMedPubDate PubStatus="accepted"><Year>2017</Year><Month>01</Month><Day>06</Day></PubMedPubDate><PubMedPubDate PubStatus="entrez"><Year>2017</Year><Month>2</Month><Day>9</Day><Hour>6</Hour><Minute>0</Minute></PubMedPubDate><PubMedPubDate PubStatus="pubmed"><Year>2017</Year><Month>2</Month><Day>9</Day><Hour>6</Hour><Minute>0</Minute></PubMedPubDate><PubMedPubDate PubStatus="medline"><Year>2018</Year><Month>10</Month><Day>31</Day><Hour>6</Hour><Minute>0</Minute></PubMedPubDate></History><PublicationStatus>epublish</PublicationStatus><ArticleIdList><ArticleId IdType="pubmed">28176855</ArticleId><ArticleId IdType="pii">srep42184</ArticleId><ArticleId IdType="doi">10.1038/srep42184</ArticleId><ArticleId IdType="pmc">PMC5296878</ArticleId></ArticleIdList><ReferenceList><Reference><Citation>Science. 2012 Aug 31;337(6098):1084-7</Citation><ArticleIdList><ArticleId IdType="pubmed">22936776</ArticleId></ArticleIdList></Reference><Reference><Citation>FEMS Microbiol Ecol. 2011 Jun;76(3):428-38</Citation><ArticleIdList><ArticleId IdType="pubmed">21303398</ArticleId></ArticleIdList></Reference><Reference><Citation>New Phytol. 2009;181(1):199-207</Citation><ArticleIdList><ArticleId 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