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Nitrite‐driven nitrous oxide production under aerobic soil conditions: kinetics and biochemical controls
Author(s) -
VENTEREA RODNEY T.
Publication year - 2007
Publication title -
global change biology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 4.146
H-Index - 255
eISSN - 1365-2486
pISSN - 1354-1013
DOI - 10.1111/j.1365-2486.2007.01389.x
Subject(s) - nitrous oxide , nitrite , nitrification , soil water , nitrate , denitrification , chemistry , nitrogen , environmental chemistry , fertilizer , abiotic component , soil science , environmental science , ecology , biology , organic chemistry
Nitrite (NO 2 − ) can accumulate during nitrification in soil following fertilizer application. While the role of NO 2 − as a substrate regulating nitrous oxide (N 2 O) production is recognized, kinetic data are not available that allow for estimating N 2 O production or soil‐to‐atmosphere fluxes as a function of NO 2 − levels under aerobic conditions. The current study investigated these kinetics as influenced by soil physical and biochemical factors in soils from cultivated and uncultivated fields in Minnesota, USA. A linear response of N 2 O production rate () to NO 2 − was observed at concentrations below 60 μg N g −1 soil in both nonsterile and sterilized soils. Rate coefficients ( K p ) relating to NO 2 − varied over two orders of magnitude and were correlated with pH, total nitrogen, and soluble and total carbon (C). Total C explained 84% of the variance in K p across all samples. Abiotic processes accounted for 31–75% of total N 2 O production. Biological reduction of NO 2 − was enhanced as oxygen (O 2 ) levels were decreased from above ambient to 5%, consistent with nitrifier denitrification. In contrast, nitrate (NO 3 − )‐reduction, and the reduction of N 2 O itself, were only stimulated at O 2 levels below 5%. Greater temperature sensitivity was observed for biological compared with chemical N 2 O production. Steady‐state model simulations predict that NO 2 − levels often found after fertilizer applications have the potential to generate substantial N 2 O fluxes even at ambient O 2 . This potential derives in part from the production of N 2 O under conditions not favorable for N 2 O reduction, in contrast to N 2 O generated from NO 3 − reduction. These results have implications with regard to improved management to minimize agricultural N 2 O emissions and improved emissions assessments.