Turnover of labile and recalcitrant soil carbon differ in response to nitrate and ammonium deposition in an ombrotrophic peatland
The effects of 4 years of simulated nitrogen deposition, as nitrate (NO₃⁻) and ammonium (NH₄⁺), on microbial carbon turnover were studied in an ombrotrophic peatland. We investigated the mineralization of simple forms of carbon using MicroResp[trade mark sign] measurements (a multiple substrate indu...
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Published in | Global change biology Vol. 16; no. 8; pp. 2307 - 2321 |
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Main Authors | , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Oxford, UK
Oxford, UK : Blackwell Publishing Ltd
01.08.2010
Blackwell Publishing Ltd Wiley-Blackwell |
Subjects | |
Online Access | Get full text |
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Summary: | The effects of 4 years of simulated nitrogen deposition, as nitrate (NO₃⁻) and ammonium (NH₄⁺), on microbial carbon turnover were studied in an ombrotrophic peatland. We investigated the mineralization of simple forms of carbon using MicroResp[trade mark sign] measurements (a multiple substrate induced respiration technique) and the activities of four soil enzymes involved in the decomposition of more complex forms of carbon or in nutrient acquisition: N-acetyl-glucosaminidase (NAG), cellobiohydrolase (CBH), acid phosphatase (AP), and phenol oxidase (PO). The potential mineralization of labile forms of carbon was significantly enhanced at the higher N additions, especially with NH₄⁺ amendments, while potential enzyme activities involved in breakdown of more complex forms of carbon or nutrient acquisition decreased slightly (NAG and CBH) or remained unchanged (AP and PO) with N amendments. This study also showed the importance of distinguishing between NO₃⁻ and NH₄⁺ amendments, as their impact often differed. It is possible that the limited response on potential extracellular enzyme activity is due to other factors, such as limited exposure to the added N in the deeper soil or continued suboptimal functioning of the enzymes due to the low pH, possibly via the inhibitory effect of low phenol oxidase activity. |
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Bibliography: | http://dx.doi.org/10.1111/j.1365-2486.2009.02082.x ArticleID:GCB2082 istex:1FA3F129C7ACE397229684BE0D9A676C27A7F19B ark:/67375/WNG-9RMH7Z3X-V SourceType-Scholarly Journals-1 ObjectType-Feature-1 content type line 14 ObjectType-Article-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 1354-1013 1365-2486 |
DOI: | 10.1111/j.1365-2486.2009.02082.x |