Methane and nitrous oxide porewater concentrations and surface fluxes of a regulated river

甲烷 一氧化二氮 温室气体 环境科学 水槽(地理) 水柱 环境化学 化学 低流变区 地表水 水文学(农业) 环境工程 地质学 海洋学 有机化学 岩土工程 地理 地图学
作者
Jorge A. Villa,Garrett J. Smith,Yang Ju,Lupita Renteria,Jordan C. Angle,Evan Arntzen,Samuel F. Harding,Huiying Ren,Xingyuan Chen,Audrey H. Sawyer,Emily Graham,James Stegen,Kelly Wrighton,Gil Bohrer
出处
期刊:Science of The Total Environment [Elsevier BV]
卷期号:715: 136920-136920 被引量:18
标识
DOI:10.1016/j.scitotenv.2020.136920
摘要

Greenhouse gas (GHG) emissions from rivers are a critical missing component of current global GHG models. Their exclusion is mainly due to a lack of in-situ measurements and a poor understanding of the spatiotemporal dynamics of GHG production and emissions, which prevents optimal model parametrization. We combined simultaneous observations of porewater concentrations along different beach positions and depths, and surface fluxes of methane and nitrous oxide at a plot scale in a large regulated river during three water stages: rising, falling, and low. Our goal was to gain insights into the interactions between hydrological exchanges and GHG emissions and elucidate possible hypotheses that could guide future research on the mechanisms of GHG production, consumption, and transport in the hyporheic zone (HZ). Results indicate that the site functioned as a net source of methane. Surface fluxes of methane during river water stages at three beach positions (shallow, intermediate and deep) correlated with porewater concentrations of methane. However, fluxes were significantly higher in the intermediate position during the low water stage, suggesting that low residence time increased methane emissions. Vertical profiles of methane peaked at different depths, indicating an influence of the magnitude and direction of the hyporheic mixing during the different river water stages on methane production and consumption. The site acted as either a sink or a source of nitrous oxide depending on the elevation of the water column. Nitrous oxide porewater concentrations peaked at the upper layers of the sediment throughout the different water stages. River hydrological stages significantly influenced porewater concentrations and fluxes of GHG, probably by influencing heterotrophic respiration (production and consumption processes) and transport to and from the HZ. Our results highlight the importance of including dynamic hydrological exchanges when studying and modeling GHG production and consumption in the HZ of large rivers.

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