Analysis of atmospheric inputs of nitrate to a temperate forest ecosystem from Δ17O isotope ratio measurements

Determining the fate of atmospheric N deposited in forest ecosystems is essential to understanding the ecological impact of increased anthropogenic N deposition. We hypothesize that a significant fraction of soil nitrate (dry deposited HNO3 and wet deposited NO3−) in northern Michigan is derived fro...

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Bibliographic Details
Published inGeophysical research letters Vol. 38; no. 15
Main Authors Costa, A. W., Michalski, G., Schauer, A. J., Alexander, B., Steig, E. J., Shepson, P. B.
Format Journal Article
LanguageEnglish
Published Washington, DC Blackwell Publishing Ltd 01.08.2011
American Geophysical Union
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Summary:Determining the fate of atmospheric N deposited in forest ecosystems is essential to understanding the ecological impact of increased anthropogenic N deposition. We hypothesize that a significant fraction of soil nitrate (dry deposited HNO3 and wet deposited NO3−) in northern Michigan is derived from atmospheric deposition. To test this idea, soil, rainfall, and cloud water were sampled in a temperate forest in northern Lower Michigan. The fraction of the soil solution NO3− pool directly from atmospheric deposition was quantified using the natural isotopic tracer, Δ17O. Our results show that on average 9% of the soil solution NO3− is unprocessed (no microbial turnover) N derived directly from the atmosphere. This points to the potential importance of anthropogenic N deposition and contributes to the long‐standing need to improve our understanding of the impacts of atmospheric nitrogen processing and deposition on forest ecosystems and forest productivity. Key Points Mass independent fraction of nitrate is a very useful tool for our question Atmospheric nitrate deposition is highly significant for N‐limited forests
Bibliography:ark:/67375/WNG-CZR5Q0V3-2
istex:FECA0B1CA522FEDD9762E465DA0F4E8CDEE20B7C
ArticleID:2011GL047539
ISSN:0094-8276
1944-8007
DOI:10.1029/2011GL047539