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Labile soil carbon inputs mediate the soil microbial community composition and plant residue decomposition rates
Root carbon (C) inputs may regulate decomposition rates in soil, and in this study we ask: how do labile C inputs regulate decomposition of plant residues, and soil microbial communities? In a 14 d laboratory incubation, we added C compounds often found in root exudates in seven different concentrat...
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Published in: | The New phytologist 2010-12, Vol.188 (4), p.1055-1064 |
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description | Root carbon (C) inputs may regulate decomposition rates in soil, and in this study we ask: how do labile C inputs regulate decomposition of plant residues, and soil microbial communities? In a 14 d laboratory incubation, we added C compounds often found in root exudates in seven different concentrations (0, 0.7, 1.4, 3.6, 7.2, 14.4 and 21.7 mg C g⁻¹ soil) to soils amended with and without ¹³C-labeled plant residue. We measured CO₂ respiration and shifts in relative fungal and bacterial rRNA gene copy numbers using quantitative polymerase chain reaction (qPCR). Increased labile C input enhanced total C respiration, but only addition of C at low concentrations (0.7 mg C g⁻¹) stimulated plant residue decomposition (+2%). Intermediate concentrations (1.4, 3.6 mg C g⁻¹) had no impact on plant residue decomposition, while greater concentrations of C (> 7.2 mg C g⁻¹) reduced decomposition (-50%). Concurrently, high exudate concentrations (> 3.6 mg C g⁻¹) increased fungal and bacterial gene copy numbers, whereas low exudate concentrations (< 3.6 mg C g⁻¹) increased metabolic activity rather than gene copy numbers. These results underscore that labile soil C inputs can regulate decomposition of more recalcitrant soil C by controlling the activity and relative abundance of fungi and bacteria. |
doi_str_mv | 10.1111/j.1469-8137.2010.03427.x |
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(ORNL), Oak Ridge, TN (United States)</creatorcontrib><description>Root carbon (C) inputs may regulate decomposition rates in soil, and in this study we ask: how do labile C inputs regulate decomposition of plant residues, and soil microbial communities? In a 14 d laboratory incubation, we added C compounds often found in root exudates in seven different concentrations (0, 0.7, 1.4, 3.6, 7.2, 14.4 and 21.7 mg C g⁻¹ soil) to soils amended with and without ¹³C-labeled plant residue. We measured CO₂ respiration and shifts in relative fungal and bacterial rRNA gene copy numbers using quantitative polymerase chain reaction (qPCR). Increased labile C input enhanced total C respiration, but only addition of C at low concentrations (0.7 mg C g⁻¹) stimulated plant residue decomposition (+2%). Intermediate concentrations (1.4, 3.6 mg C g⁻¹) had no impact on plant residue decomposition, while greater concentrations of C (> 7.2 mg C g⁻¹) reduced decomposition (-50%). Concurrently, high exudate concentrations (> 3.6 mg C g⁻¹) increased fungal and bacterial gene copy numbers, whereas low exudate concentrations (< 3.6 mg C g⁻¹) increased metabolic activity rather than gene copy numbers. These results underscore that labile soil C inputs can regulate decomposition of more recalcitrant soil C by controlling the activity and relative abundance of fungi and bacteria.</description><identifier>ISSN: 0028-646X</identifier><identifier>EISSN: 1469-8137</identifier><identifier>DOI: 10.1111/j.1469-8137.2010.03427.x</identifier><identifier>PMID: 21058948</identifier><language>eng</language><publisher>Oxford, UK: John Wiley & Sons</publisher><subject>ABUNDANCE ; Acid soils ; BACTERIA ; Bacteria - drug effects ; Bacteria - genetics ; BASIC BIOLOGICAL SCIENCES ; Biodegradation, Environmental - drug effects ; CARBON ; Carbon - metabolism ; Carbon - pharmacology ; CARBON DIOXIDE ; Carbon Dioxide - metabolism ; carbon‐13 ; Cell Respiration - drug effects ; Community composition ; DECOMPOSITION ; ENVIRONMENTAL SCIENCES ; Exudates ; Exudation ; FUNGI ; Fungi - drug effects ; Fungi - genetics ; Gene Dosage - drug effects ; GENES ; INCUBATION ; Incubation period ; Low concentrations ; Microbial activity ; Microbiomes ; Microorganisms ; Nucleotide sequence ; Panicum - cytology ; Panicum - drug effects ; Panicum - metabolism ; PCR ; Plant communities ; Plant residues ; POLYMERASE CHAIN REACTION ; priming ; qPCR ; Relative abundance ; RESIDUES ; RESPIRATION ; root exudation ; rRNA ; Soil ; Soil - analysis ; Soil amendment ; Soil biochemistry ; Soil biology ; Soil composition ; Soil ecology ; Soil fungi ; Soil Microbiology ; Soil microorganisms ; Soil respiration ; Soil water ; SOILS</subject><ispartof>The New phytologist, 2010-12, Vol.188 (4), p.1055-1064</ispartof><rights>Copyright © 2010 New Phytologist Trust</rights><rights>No claim to original US government works. Journal compilation © New Phytologist Trust (2010)</rights><rights>No claim to original US government works. Journal compilation © New Phytologist Trust (2010).</rights><rights>Copyright Wiley Subscription Services, Inc. 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(ORNL), Oak Ridge, TN (United States)</creatorcontrib><title>Labile soil carbon inputs mediate the soil microbial community composition and plant residue decomposition rates</title><title>The New phytologist</title><addtitle>New Phytol</addtitle><description>Root carbon (C) inputs may regulate decomposition rates in soil, and in this study we ask: how do labile C inputs regulate decomposition of plant residues, and soil microbial communities? In a 14 d laboratory incubation, we added C compounds often found in root exudates in seven different concentrations (0, 0.7, 1.4, 3.6, 7.2, 14.4 and 21.7 mg C g⁻¹ soil) to soils amended with and without ¹³C-labeled plant residue. We measured CO₂ respiration and shifts in relative fungal and bacterial rRNA gene copy numbers using quantitative polymerase chain reaction (qPCR). Increased labile C input enhanced total C respiration, but only addition of C at low concentrations (0.7 mg C g⁻¹) stimulated plant residue decomposition (+2%). Intermediate concentrations (1.4, 3.6 mg C g⁻¹) had no impact on plant residue decomposition, while greater concentrations of C (> 7.2 mg C g⁻¹) reduced decomposition (-50%). Concurrently, high exudate concentrations (> 3.6 mg C g⁻¹) increased fungal and bacterial gene copy numbers, whereas low exudate concentrations (< 3.6 mg C g⁻¹) increased metabolic activity rather than gene copy numbers. These results underscore that labile soil C inputs can regulate decomposition of more recalcitrant soil C by controlling the activity and relative abundance of fungi and bacteria.</description><subject>ABUNDANCE</subject><subject>Acid soils</subject><subject>BACTERIA</subject><subject>Bacteria - drug effects</subject><subject>Bacteria - genetics</subject><subject>BASIC BIOLOGICAL SCIENCES</subject><subject>Biodegradation, Environmental - drug effects</subject><subject>CARBON</subject><subject>Carbon - metabolism</subject><subject>Carbon - pharmacology</subject><subject>CARBON DIOXIDE</subject><subject>Carbon Dioxide - metabolism</subject><subject>carbon‐13</subject><subject>Cell Respiration - drug effects</subject><subject>Community composition</subject><subject>DECOMPOSITION</subject><subject>ENVIRONMENTAL SCIENCES</subject><subject>Exudates</subject><subject>Exudation</subject><subject>FUNGI</subject><subject>Fungi - drug effects</subject><subject>Fungi - genetics</subject><subject>Gene Dosage - drug effects</subject><subject>GENES</subject><subject>INCUBATION</subject><subject>Incubation period</subject><subject>Low concentrations</subject><subject>Microbial activity</subject><subject>Microbiomes</subject><subject>Microorganisms</subject><subject>Nucleotide sequence</subject><subject>Panicum - cytology</subject><subject>Panicum - drug effects</subject><subject>Panicum - metabolism</subject><subject>PCR</subject><subject>Plant communities</subject><subject>Plant residues</subject><subject>POLYMERASE CHAIN REACTION</subject><subject>priming</subject><subject>qPCR</subject><subject>Relative abundance</subject><subject>RESIDUES</subject><subject>RESPIRATION</subject><subject>root exudation</subject><subject>rRNA</subject><subject>Soil</subject><subject>Soil - analysis</subject><subject>Soil amendment</subject><subject>Soil biochemistry</subject><subject>Soil biology</subject><subject>Soil composition</subject><subject>Soil ecology</subject><subject>Soil fungi</subject><subject>Soil Microbiology</subject><subject>Soil microorganisms</subject><subject>Soil respiration</subject><subject>Soil water</subject><subject>SOILS</subject><issn>0028-646X</issn><issn>1469-8137</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2010</creationdate><recordtype>article</recordtype><recordid>eNqNkU1v1DAQhi0EotvCTwBFcOCUxd9xDhxQBS3SCjiAxM1yHEd1lMTBdkT33zMhywpxAV888jzveGZehAqC9wTO635PuKxLRVi1pxheMeO02t8_QLtz4iHaYUxVKbn8doEuU-oxxrWQ9DG6oAQLVXO1Q_PBNH5wRQp-KKyJTZgKP81LTsXoWm-yK_LdKT16G0PjDYBhHJfJ5-MazSH57EFnpraYBzPlIrrk28UVrfszH6FaeoIedWZI7unpvkJf37_7cn1bHj7dfLh-eyitqFlVNoZLqYxkcBQWDbx1TcdqRjvLHXdKEYvrrmOKuhbDuI2iomuolcK2hrTsCr3Y6oaUvU7WZ2fvbJgmZ7MmmHKGMUCvNmiO4fviUtajT9YNMIQLS9JKKE4pI-SfZCUZhcaFBPLlX2QfljjBrJoKQhmF1VdAqY2ClaYUXafn6EcTj9CbXj3WvV6t1KuVevVY__JY34P0-emDpQGPzsLfpgLwZgN-gLPH_y6sP36-XSPQP9v0fcohnvUc1xLDRthPvW2_DQ</recordid><startdate>201012</startdate><enddate>201012</enddate><creator>de Graaff, Marie-Anne</creator><creator>Classen, Aimee T.</creator><creator>Castro, Hector F.</creator><creator>Schadt, Christopher W.</creator><general>John Wiley & Sons</general><general>Blackwell Publishing Ltd</general><general>Wiley Subscription Services, Inc</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>7QO</scope><scope>7SN</scope><scope>8FD</scope><scope>C1K</scope><scope>F1W</scope><scope>FR3</scope><scope>H95</scope><scope>L.G</scope><scope>M7N</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope><scope>7T7</scope><scope>OTOTI</scope></search><sort><creationdate>201012</creationdate><title>Labile soil carbon inputs mediate the soil microbial community composition and plant residue decomposition rates</title><author>de Graaff, Marie-Anne ; Classen, Aimee T. ; Castro, Hector F. ; Schadt, Christopher W.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5937-ba4668a63333805b937fbf3932fc4e4e881c09ff382ed0137b825fb2c65cda1d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2010</creationdate><topic>ABUNDANCE</topic><topic>Acid soils</topic><topic>BACTERIA</topic><topic>Bacteria - drug effects</topic><topic>Bacteria - genetics</topic><topic>BASIC BIOLOGICAL SCIENCES</topic><topic>Biodegradation, Environmental - drug effects</topic><topic>CARBON</topic><topic>Carbon - metabolism</topic><topic>Carbon - pharmacology</topic><topic>CARBON DIOXIDE</topic><topic>Carbon Dioxide - metabolism</topic><topic>carbon‐13</topic><topic>Cell Respiration - drug effects</topic><topic>Community composition</topic><topic>DECOMPOSITION</topic><topic>ENVIRONMENTAL SCIENCES</topic><topic>Exudates</topic><topic>Exudation</topic><topic>FUNGI</topic><topic>Fungi - drug effects</topic><topic>Fungi - genetics</topic><topic>Gene Dosage - drug effects</topic><topic>GENES</topic><topic>INCUBATION</topic><topic>Incubation period</topic><topic>Low concentrations</topic><topic>Microbial activity</topic><topic>Microbiomes</topic><topic>Microorganisms</topic><topic>Nucleotide sequence</topic><topic>Panicum - cytology</topic><topic>Panicum - drug effects</topic><topic>Panicum - metabolism</topic><topic>PCR</topic><topic>Plant communities</topic><topic>Plant residues</topic><topic>POLYMERASE CHAIN REACTION</topic><topic>priming</topic><topic>qPCR</topic><topic>Relative abundance</topic><topic>RESIDUES</topic><topic>RESPIRATION</topic><topic>root exudation</topic><topic>rRNA</topic><topic>Soil</topic><topic>Soil - analysis</topic><topic>Soil amendment</topic><topic>Soil biochemistry</topic><topic>Soil biology</topic><topic>Soil composition</topic><topic>Soil ecology</topic><topic>Soil fungi</topic><topic>Soil Microbiology</topic><topic>Soil microorganisms</topic><topic>Soil respiration</topic><topic>Soil water</topic><topic>SOILS</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>de Graaff, Marie-Anne</creatorcontrib><creatorcontrib>Classen, Aimee T.</creatorcontrib><creatorcontrib>Castro, Hector F.</creatorcontrib><creatorcontrib>Schadt, Christopher W.</creatorcontrib><creatorcontrib>Oak Ridge National Lab. 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(ORNL), Oak Ridge, TN (United States)</aucorp><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Labile soil carbon inputs mediate the soil microbial community composition and plant residue decomposition rates</atitle><jtitle>The New phytologist</jtitle><addtitle>New Phytol</addtitle><date>2010-12</date><risdate>2010</risdate><volume>188</volume><issue>4</issue><spage>1055</spage><epage>1064</epage><pages>1055-1064</pages><issn>0028-646X</issn><eissn>1469-8137</eissn><abstract>Root carbon (C) inputs may regulate decomposition rates in soil, and in this study we ask: how do labile C inputs regulate decomposition of plant residues, and soil microbial communities? In a 14 d laboratory incubation, we added C compounds often found in root exudates in seven different concentrations (0, 0.7, 1.4, 3.6, 7.2, 14.4 and 21.7 mg C g⁻¹ soil) to soils amended with and without ¹³C-labeled plant residue. We measured CO₂ respiration and shifts in relative fungal and bacterial rRNA gene copy numbers using quantitative polymerase chain reaction (qPCR). Increased labile C input enhanced total C respiration, but only addition of C at low concentrations (0.7 mg C g⁻¹) stimulated plant residue decomposition (+2%). Intermediate concentrations (1.4, 3.6 mg C g⁻¹) had no impact on plant residue decomposition, while greater concentrations of C (> 7.2 mg C g⁻¹) reduced decomposition (-50%). Concurrently, high exudate concentrations (> 3.6 mg C g⁻¹) increased fungal and bacterial gene copy numbers, whereas low exudate concentrations (< 3.6 mg C g⁻¹) increased metabolic activity rather than gene copy numbers. These results underscore that labile soil C inputs can regulate decomposition of more recalcitrant soil C by controlling the activity and relative abundance of fungi and bacteria.</abstract><cop>Oxford, UK</cop><pub>John Wiley & Sons</pub><pmid>21058948</pmid><doi>10.1111/j.1469-8137.2010.03427.x</doi><tpages>10</tpages><oa>free_for_read</oa></addata></record> |
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subjects | ABUNDANCE Acid soils BACTERIA Bacteria - drug effects Bacteria - genetics BASIC BIOLOGICAL SCIENCES Biodegradation, Environmental - drug effects CARBON Carbon - metabolism Carbon - pharmacology CARBON DIOXIDE Carbon Dioxide - metabolism carbon‐13 Cell Respiration - drug effects Community composition DECOMPOSITION ENVIRONMENTAL SCIENCES Exudates Exudation FUNGI Fungi - drug effects Fungi - genetics Gene Dosage - drug effects GENES INCUBATION Incubation period Low concentrations Microbial activity Microbiomes Microorganisms Nucleotide sequence Panicum - cytology Panicum - drug effects Panicum - metabolism PCR Plant communities Plant residues POLYMERASE CHAIN REACTION priming qPCR Relative abundance RESIDUES RESPIRATION root exudation rRNA Soil Soil - analysis Soil amendment Soil biochemistry Soil biology Soil composition Soil ecology Soil fungi Soil Microbiology Soil microorganisms Soil respiration Soil water SOILS |
title | Labile soil carbon inputs mediate the soil microbial community composition and plant residue decomposition rates |
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