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Dynamics of nitrous oxide in groundwater at the aquatic-terrestrial interface

机译:水陆界面的一氧化二氮动力学

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摘要

Few data are available to validate the Intergovernmental Panel on Climate Change's (IPCC) emission factors for indirect emissions of nitrous oxide (N2O). In particular the N2O emissions resulting from nitrogen leaching and the associated groundwater and surface drainage (EF5-g) are particularly poorly characterized. In situ push-pull methods have been used to identify the fate of NO3- in the groundwater. In this study, we adapted a previously published in situ denitrification push-pull method to examine the fate of (N2O)-N-15 introduced into the subsoil-groundwater matrix. Enriched (N2O)-N-15 was manufactured, added to groundwater via a closed system in the laboratory, and then introduced into the groundwater-subsoil matrix in an upland-marsh transition zone of a salt marsh and a forested alluvial riparian zone. Conservative tracers (SF6 and Br-) and (N2O)-N-15 were injected into the groundwater and left for 1-4h after which the groundwater was sampled. Added (N2O)-N-15 behaved in a conservative manner at one site while the other site showed variability with some injections showing significant consumption (3-8 mu g N2O-(15)Nkg(-1) soil day(-1)) of (N2O)-N-15. Our results show that the fate and dynamics of N2O in groundwater are complex and variable and that these dynamics should be considered in the development of improved IPCC inventory calculations.
机译:很少有数据可以验证政府间气候变化专门委员会(IPCC)的一氧化二氮(N2O)间接排放因子。特别是,由氮浸出以及相关的地下水和地表排水(EF5-g)引起的N2O排放特别难以表征。原位推挽法已被用于确定地下水中NO3-的去向。在这项研究中,我们采用了以前发布的原位反硝化推挽方法,以研究引入地下土壤-地下水基质中的(N2O)-N-15的命运。生产了浓缩的(N2O)-N-15,并通过实验室中的密闭系统将其添加到地下水中,然后将其引入盐沼的山地沼泽过渡带和森林冲积河岸带的地下水-土壤基质中。将守恒示踪剂(SF6和Br-)和(N2O)-N-15注入地下水中,放置1-4h,然后对地下水进行采样。 (N2O)-N-15在一个站点上表现保守,而另一站点显示出一定的可变性,某些注射显示出大量消耗(3-8μgN2O-(15)Nkg(-1)土壤日(-1) (N2O)-N-15)。我们的结果表明,地下水中N2O的命运和动态是复杂且可变的,在开发改进的IPCC库存计算时应考虑这些动态。

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