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Nitrous oxide production in the Chesapeake Bay
Limnology and Oceanography ( IF 4.5 ) Pub Date : 2022-07-27 , DOI: 10.1002/lno.12191
Weiyi Tang 1 , John C. Tracey 1 , Julia Carroll 1 , Elizabeth Wallace 1 , Jenna A. Lee 1 , Levy Nathan 1 , Xin Sun 1, 2 , Amal Jayakumar 1 , Bess B. Ward 1
Affiliation  

Estuaries at the global scale are significant but highly uncertain sources of atmospheric nitrous oxide (N2O), which is an intense greenhouse gas and ozone depletion agent. As the largest estuary in the United States, the Chesapeake Bay is suggested to be a spatially and temporally variable source and sink of N2O. However, limited observations of N2O cycling preclude us from estimating and predicting its net N2O flux. To improve our mechanistic understanding of the processes that control the N2O flux at the point of production, we applied multiple 15N tracers (NH4+15, 15N-urea, NO215, and NO315) to separately track N2O production from nitrification and denitrification under in situ and manipulated O2 concentrations in the Chesapeake Bay. Nitrification was the major N2O production pathway in oxic waters (up to 7.5 nmol N2O L−1 d−1). In contrast, denitrification dominated N2O production from hypoxic/anoxic waters (up to 20 nmol N2O L−1 d−1). N2O production from urea was observed for the first time in estuarine waters. The contribution from urea was small, but interestingly, showed a depth pattern distinct from other N2O precursors. Experimentally lowering the O2 concentration substantially enhanced N2O production. Therefore, the expansion of hypoxic and anoxic zones in the Chesapeake Bay under climate change as suggested by some climate models may favor the production of N2O, potentially providing positive feedback on warming. Overall, our study provides mechanistic constraints on N2O dynamics that could benefit modeling studies to better estimate the N2O flux in the Chesapeake Bay and other coastal environments.

中文翻译:

切萨皮克湾的一氧化二氮生产

全球范围的河口是大气中一氧化二氮 (N 2 O) 的重要但高度不确定的来源,它是一种强烈的温室气体和臭氧消耗剂。作为美国最大的河口,切萨皮克湾被认为是空间和时间可变的 N 2 O 源和汇。然而,对 N 2 O 循环的有限观察使我们无法估计和预测其净 N 2 O 通量. 为了提高我们对在生产点控制 N 2 O 通量的过程的机械理解,我们应用了多个15 N 示踪剂(NH4+15, 15 N-尿素,2-15,3-15) 分别跟踪切萨皮克湾原位硝化和反硝化产生的N 2 O 和操纵的 O 2浓度。硝化是含氧水中的主要 N 2 O 生产途径(高达 7.5 nmol N 2 O L -1 d -1)。相反,反硝化作用在缺氧/缺氧水的 N 2 O 生产中占主导地位(高达 20 nmol N 2 O L -1 d -1)。在河口水域首次观察到尿素产生N 2 O。尿素的贡献很小,但有趣的是,显示出与其他 N 2不同的深度模式O前体。通过实验降低O 2浓度显着提高了N 2 O的产生。因此,一些气候模型表明,气候变化下切萨皮克湾缺氧区和缺氧区的扩大可能有利于 N 2 O 的产生,从而可能为变暖提供积极的反馈。总体而言,我们的研究提供了对 N 2 O 动力学的机械约束,这有助于建模研究更好地估计切萨皮克湾和其他沿海环境中的 N 2 O 通量。
更新日期:2022-07-27
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