期刊
GEOCHIMICA ET COSMOCHIMICA ACTA
卷 139, 期 -, 页码 72-82出版社
PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.gca.2014.04.037
关键词
-
资金
- COST Action [ES0806]
- State Secretariat for Education and Research (SER) within COST Action [ES0806]
- Swiss National Science Foundation (SNF)
Efficient nitrous oxide (N2O) mitigation strategies require the identification of the main source and sink processes and their contribution to total soil N2O production. Several abiotic reactions of nitrification intermediates leading to N2O production are known, but their contribution to total N2O production in soils is uncertain. As the site preference (SP) of N-15 in N2O is a promising tool to give more insight into N2O production processes, we investigated the SP of N2O produced by different abiotic reactions in a laboratory study. All reactions involved the nitrification intermediate hydroxylamine (NH2OH) in combination with nitrite (NO2-), Fe3+, Fe2+ and Cu2+, reactants commonly or potentially found in soils, at different concentrations and pH values. N2O production and its four main isotopic species ((NNO)-N-14-N-14-O-16, (NNO)-N-15-N-14-O-16, (NNO)-N-14-N-15-O-16, and (NNO)-N-14-N-14-O-18) were quantified simultaneously and online at high temporal resolution using quantum cascade laser absorption spectroscopy. Thereby, our study presents the first continuous analysis of delta O-18 in N2O. The experiments revealed the possibility of purely abiotic reactions over a wide range of acidity (pH 3-8) by different mechanisms. All studied abiotic pathways produced N2O with a characteristic SP in the range of 34-35 parts per thousand, unaffected by process conditions and remaining constant over the course of the experiments. These findings reflect the benefit of continuous N2O isotopic analysis by laser spectroscopy, contribute new information to the challenging source partitioning of N2O emissions from soils, and emphasize the potentially significant role of coupled biotic-abiotic reactions in soils. (C) 2014 Elsevier Ltd. All rights reserved.
作者
我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。
推荐
暂无数据