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Measuring the contributions of nitrification and denitrification to the flux of nitrous oxide from soil
The flux of N 2O from soil can be due to nitrification or denitrification. Since aerobic and anaerobic microsites can develop within the same soil aggregate, nitrification and denitrification could be occurring at the same time. The contribution of nitrification and denitrification to the flux of N...
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Published in: | Soil biology & biochemistry 1997-02, Vol.29 (2), p.139-151 |
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creator | Stevens, R.J. Laughlin, R.J. Burns, L.C. Arah, J.R.M. Hood, R.C. |
description | The flux of N
2O from soil can be due to nitrification or denitrification. Since aerobic and anaerobic microsites can develop within the same soil aggregate, nitrification and denitrification could be occurring at the same time. The contribution of nitrification and denitrification to the flux of N
2O can be studied by differentially
15N-labelling the NO
3
− and NH
4
+ pools in soils. By periodically measuring and comparing the enrichments of the N
2O, NH
4
+ and NO
3
− pools, the relative importance of the two processes can be quantified. The conclusions are based on calculations which assume that the
15N atom fractions of the nitrification and denitrification pools remain uniform throughout the incubation. The initial uniformity of the denitrification pool was tested by adding a nitrification-inhibitor, C
2H
2, at time zero and examining the
15N-distribution of the accumulated N
2O at subsequent times. If the
15N distribution in the N
2O is random it originated from one source, but ifthe
15N distribution is non-random the N
2O originated from two or more sources. Two soil incubation experiments were conducted. In the first experiment fresh sieved soil was incubated over 10 days at 40, 50 and 60% moisture content with (NH
2)
2CO (70 μmol N g
−1) and KNO
3 (14 μmol N g
−1) differentially labelled at 10 atom% excess
15N. The headspace was sampled daily for N
2O before being refreshed with normal air. Every second day the sizes and enrichments of the NH
4
+ and NO
3
− pools were determined by destructive sampling. In the second experiment the assumption that the method of addition of label created only one denitrifying pool was tested by blocking nitrification with C
2H
2 (10 kPa). Fresh soil was incubated for three incubation times (6, 12 and 24 h) with differentially-labelled NH
4NO
3 (1.46 μmol N g
−1) enriched to 20 atom% excess
15N, with glucose (42 and 83 μmol C g
−1) to promote denitrification. In the first experiment the enrichment of the N
2O did not match either the enrichment of the NH
4
+ or NO
3
− pools, showing that N
2O was being produced by nitrification and denitrification. Quantification of the fractional contributions of nitrification and denitrification showed that denitrification was the dominant process in the first 2 days, but then nitrification became the dominant process for the rest of the incubation. More N
2O was produced at 50 and 60% moisture than at 40% moisture, but the relative contributions of the two processes were the same |
doi_str_mv | 10.1016/S0038-0717(96)00303-3 |
format | article |
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2O from soil can be due to nitrification or denitrification. Since aerobic and anaerobic microsites can develop within the same soil aggregate, nitrification and denitrification could be occurring at the same time. The contribution of nitrification and denitrification to the flux of N
2O can be studied by differentially
15N-labelling the NO
3
− and NH
4
+ pools in soils. By periodically measuring and comparing the enrichments of the N
2O, NH
4
+ and NO
3
− pools, the relative importance of the two processes can be quantified. The conclusions are based on calculations which assume that the
15N atom fractions of the nitrification and denitrification pools remain uniform throughout the incubation. The initial uniformity of the denitrification pool was tested by adding a nitrification-inhibitor, C
2H
2, at time zero and examining the
15N-distribution of the accumulated N
2O at subsequent times. If the
15N distribution in the N
2O is random it originated from one source, but ifthe
15N distribution is non-random the N
2O originated from two or more sources. Two soil incubation experiments were conducted. In the first experiment fresh sieved soil was incubated over 10 days at 40, 50 and 60% moisture content with (NH
2)
2CO (70 μmol N g
−1) and KNO
3 (14 μmol N g
−1) differentially labelled at 10 atom% excess
15N. The headspace was sampled daily for N
2O before being refreshed with normal air. Every second day the sizes and enrichments of the NH
4
+ and NO
3
− pools were determined by destructive sampling. In the second experiment the assumption that the method of addition of label created only one denitrifying pool was tested by blocking nitrification with C
2H
2 (10 kPa). Fresh soil was incubated for three incubation times (6, 12 and 24 h) with differentially-labelled NH
4NO
3 (1.46 μmol N g
−1) enriched to 20 atom% excess
15N, with glucose (42 and 83 μmol C g
−1) to promote denitrification. In the first experiment the enrichment of the N
2O did not match either the enrichment of the NH
4
+ or NO
3
− pools, showing that N
2O was being produced by nitrification and denitrification. Quantification of the fractional contributions of nitrification and denitrification showed that denitrification was the dominant process in the first 2 days, but then nitrification became the dominant process for the rest of the incubation. More N
2O was produced at 50 and 60% moisture than at 40% moisture, but the relative contributions of the two processes were the same at all moisture contents. Nitrification was responsible for 70% of the N
2O flux. In the second experiment examination of the isotopic composition of the N
2O showed that the
15N atoms were randomly distributed throughout the molecules. The N
2O therefore orginated from one denitrifying pool, confirming that our method of addition of label initially created one NO
3
− pool for denitrification. There seems to be no feasible way at present to test the uniformity of the nitrification pool.</description><identifier>ISSN: 0038-0717</identifier><identifier>EISSN: 1879-3428</identifier><identifier>DOI: 10.1016/S0038-0717(96)00303-3</identifier><identifier>CODEN: SBIOAH</identifier><language>eng</language><publisher>Oxford: Elsevier Ltd</publisher><subject>Agronomy. Soil science and plant productions ; Biological and medical sciences ; Chemical, physicochemical, biochemical and biological properties ; Fundamental and applied biological sciences. Psychology ; Organic matter ; Physics, chemistry, biochemistry and biology of agricultural and forest soils ; Soil science</subject><ispartof>Soil biology & biochemistry, 1997-02, Vol.29 (2), p.139-151</ispartof><rights>1997</rights><rights>1997 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c433t-894e7714a0896e253f38250c4f8b6304d5930bab0079aa57aa36283a335dd783</citedby><cites>FETCH-LOGICAL-c433t-894e7714a0896e253f38250c4f8b6304d5930bab0079aa57aa36283a335dd783</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>315,786,790,27957,27958</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=2703216$$DView record in Pascal Francis$$Hfree_for_read</backlink></links><search><creatorcontrib>Stevens, R.J.</creatorcontrib><creatorcontrib>Laughlin, R.J.</creatorcontrib><creatorcontrib>Burns, L.C.</creatorcontrib><creatorcontrib>Arah, J.R.M.</creatorcontrib><creatorcontrib>Hood, R.C.</creatorcontrib><title>Measuring the contributions of nitrification and denitrification to the flux of nitrous oxide from soil</title><title>Soil biology & biochemistry</title><description>The flux of N
2O from soil can be due to nitrification or denitrification. Since aerobic and anaerobic microsites can develop within the same soil aggregate, nitrification and denitrification could be occurring at the same time. The contribution of nitrification and denitrification to the flux of N
2O can be studied by differentially
15N-labelling the NO
3
− and NH
4
+ pools in soils. By periodically measuring and comparing the enrichments of the N
2O, NH
4
+ and NO
3
− pools, the relative importance of the two processes can be quantified. The conclusions are based on calculations which assume that the
15N atom fractions of the nitrification and denitrification pools remain uniform throughout the incubation. The initial uniformity of the denitrification pool was tested by adding a nitrification-inhibitor, C
2H
2, at time zero and examining the
15N-distribution of the accumulated N
2O at subsequent times. If the
15N distribution in the N
2O is random it originated from one source, but ifthe
15N distribution is non-random the N
2O originated from two or more sources. Two soil incubation experiments were conducted. In the first experiment fresh sieved soil was incubated over 10 days at 40, 50 and 60% moisture content with (NH
2)
2CO (70 μmol N g
−1) and KNO
3 (14 μmol N g
−1) differentially labelled at 10 atom% excess
15N. The headspace was sampled daily for N
2O before being refreshed with normal air. Every second day the sizes and enrichments of the NH
4
+ and NO
3
− pools were determined by destructive sampling. In the second experiment the assumption that the method of addition of label created only one denitrifying pool was tested by blocking nitrification with C
2H
2 (10 kPa). Fresh soil was incubated for three incubation times (6, 12 and 24 h) with differentially-labelled NH
4NO
3 (1.46 μmol N g
−1) enriched to 20 atom% excess
15N, with glucose (42 and 83 μmol C g
−1) to promote denitrification. In the first experiment the enrichment of the N
2O did not match either the enrichment of the NH
4
+ or NO
3
− pools, showing that N
2O was being produced by nitrification and denitrification. Quantification of the fractional contributions of nitrification and denitrification showed that denitrification was the dominant process in the first 2 days, but then nitrification became the dominant process for the rest of the incubation. More N
2O was produced at 50 and 60% moisture than at 40% moisture, but the relative contributions of the two processes were the same at all moisture contents. Nitrification was responsible for 70% of the N
2O flux. In the second experiment examination of the isotopic composition of the N
2O showed that the
15N atoms were randomly distributed throughout the molecules. The N
2O therefore orginated from one denitrifying pool, confirming that our method of addition of label initially created one NO
3
− pool for denitrification. There seems to be no feasible way at present to test the uniformity of the nitrification pool.</description><subject>Agronomy. Soil science and plant productions</subject><subject>Biological and medical sciences</subject><subject>Chemical, physicochemical, biochemical and biological properties</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Organic matter</subject><subject>Physics, chemistry, biochemistry and biology of agricultural and forest soils</subject><subject>Soil science</subject><issn>0038-0717</issn><issn>1879-3428</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1997</creationdate><recordtype>article</recordtype><recordid>eNqFkEtLxDAUhYMoOI7-BKELEV1Ub3rbJlmJDL5AceHsQ5qmY6TTjEkr478383DAlatwD-e75-YQckrhigItr98AkKfAKLsQ5WUcAFPcIyPKmUgxz_g-Ge0sh-QohA8AyAqKIzJ7MSoM3nazpH83iXZd72019NZ1IXFN0tk4N1arlZKork5q81fr3Zps2mH5C7ghsktbR9W7eRKcbY_JQaPaYE6275hM7--mk8f0-fXhaXL7nOocsU-5yA1jNFfARWmyAhvkWQE6b3hVIuR1IRAqVQEwoVTBlMIy46gQi7pmHMfkfLN24d3nYEIv5zZo07aqM_EqSeOSQmQ0GouNUXsXgjeNXHg7V_5bUpCrVuW6VbmqTIpSrluVGLmzbYAKWrWNV522YQdnDDCLIWNys7GZ-Ncva7wM2ppOm9p6o3tZO_tP0A_dsoxB</recordid><startdate>19970201</startdate><enddate>19970201</enddate><creator>Stevens, R.J.</creator><creator>Laughlin, R.J.</creator><creator>Burns, L.C.</creator><creator>Arah, J.R.M.</creator><creator>Hood, R.C.</creator><general>Elsevier Ltd</general><general>Elsevier Science</general><scope>IQODW</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7SN</scope><scope>7T7</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>P64</scope></search><sort><creationdate>19970201</creationdate><title>Measuring the contributions of nitrification and denitrification to the flux of nitrous oxide from soil</title><author>Stevens, R.J. ; Laughlin, R.J. ; Burns, L.C. ; Arah, J.R.M. ; Hood, R.C.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c433t-894e7714a0896e253f38250c4f8b6304d5930bab0079aa57aa36283a335dd783</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1997</creationdate><topic>Agronomy. Soil science and plant productions</topic><topic>Biological and medical sciences</topic><topic>Chemical, physicochemical, biochemical and biological properties</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Organic matter</topic><topic>Physics, chemistry, biochemistry and biology of agricultural and forest soils</topic><topic>Soil science</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Stevens, R.J.</creatorcontrib><creatorcontrib>Laughlin, R.J.</creatorcontrib><creatorcontrib>Burns, L.C.</creatorcontrib><creatorcontrib>Arah, J.R.M.</creatorcontrib><creatorcontrib>Hood, R.C.</creatorcontrib><collection>Pascal-Francis</collection><collection>CrossRef</collection><collection>Ecology Abstracts</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><jtitle>Soil biology & biochemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Stevens, R.J.</au><au>Laughlin, R.J.</au><au>Burns, L.C.</au><au>Arah, J.R.M.</au><au>Hood, R.C.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Measuring the contributions of nitrification and denitrification to the flux of nitrous oxide from soil</atitle><jtitle>Soil biology & biochemistry</jtitle><date>1997-02-01</date><risdate>1997</risdate><volume>29</volume><issue>2</issue><spage>139</spage><epage>151</epage><pages>139-151</pages><issn>0038-0717</issn><eissn>1879-3428</eissn><coden>SBIOAH</coden><notes>ObjectType-Article-2</notes><notes>SourceType-Scholarly Journals-1</notes><notes>ObjectType-Feature-1</notes><notes>content type line 23</notes><abstract>The flux of N
2O from soil can be due to nitrification or denitrification. Since aerobic and anaerobic microsites can develop within the same soil aggregate, nitrification and denitrification could be occurring at the same time. The contribution of nitrification and denitrification to the flux of N
2O can be studied by differentially
15N-labelling the NO
3
− and NH
4
+ pools in soils. By periodically measuring and comparing the enrichments of the N
2O, NH
4
+ and NO
3
− pools, the relative importance of the two processes can be quantified. The conclusions are based on calculations which assume that the
15N atom fractions of the nitrification and denitrification pools remain uniform throughout the incubation. The initial uniformity of the denitrification pool was tested by adding a nitrification-inhibitor, C
2H
2, at time zero and examining the
15N-distribution of the accumulated N
2O at subsequent times. If the
15N distribution in the N
2O is random it originated from one source, but ifthe
15N distribution is non-random the N
2O originated from two or more sources. Two soil incubation experiments were conducted. In the first experiment fresh sieved soil was incubated over 10 days at 40, 50 and 60% moisture content with (NH
2)
2CO (70 μmol N g
−1) and KNO
3 (14 μmol N g
−1) differentially labelled at 10 atom% excess
15N. The headspace was sampled daily for N
2O before being refreshed with normal air. Every second day the sizes and enrichments of the NH
4
+ and NO
3
− pools were determined by destructive sampling. In the second experiment the assumption that the method of addition of label created only one denitrifying pool was tested by blocking nitrification with C
2H
2 (10 kPa). Fresh soil was incubated for three incubation times (6, 12 and 24 h) with differentially-labelled NH
4NO
3 (1.46 μmol N g
−1) enriched to 20 atom% excess
15N, with glucose (42 and 83 μmol C g
−1) to promote denitrification. In the first experiment the enrichment of the N
2O did not match either the enrichment of the NH
4
+ or NO
3
− pools, showing that N
2O was being produced by nitrification and denitrification. Quantification of the fractional contributions of nitrification and denitrification showed that denitrification was the dominant process in the first 2 days, but then nitrification became the dominant process for the rest of the incubation. More N
2O was produced at 50 and 60% moisture than at 40% moisture, but the relative contributions of the two processes were the same at all moisture contents. Nitrification was responsible for 70% of the N
2O flux. In the second experiment examination of the isotopic composition of the N
2O showed that the
15N atoms were randomly distributed throughout the molecules. The N
2O therefore orginated from one denitrifying pool, confirming that our method of addition of label initially created one NO
3
− pool for denitrification. There seems to be no feasible way at present to test the uniformity of the nitrification pool.</abstract><cop>Oxford</cop><cop>New York, NY</cop><pub>Elsevier Ltd</pub><doi>10.1016/S0038-0717(96)00303-3</doi><tpages>13</tpages></addata></record> |
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language | eng |
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source | ScienceDirect Freedom Collection 2022-2024 |
subjects | Agronomy. Soil science and plant productions Biological and medical sciences Chemical, physicochemical, biochemical and biological properties Fundamental and applied biological sciences. Psychology Organic matter Physics, chemistry, biochemistry and biology of agricultural and forest soils Soil science |
title | Measuring the contributions of nitrification and denitrification to the flux of nitrous oxide from soil |
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