Precipitation fuels dissolved greenhouse gas (CO2, CH4, N2O) dynamics in a peatland-dominated headwater stream: results from a continuous monitoring setup

生物地球化学循环 温室气体 一氧化二氮 环境科学 泥炭 二氧化碳 环境化学 甲烷 溶解有机碳 溪流 水文学(农业) 碳循环 大气(单位) 微粒 大气科学 生态系统 化学 生态学 气象学 地质学 工程类 有机化学 物理 岩土工程 生物 计算机科学 计算机网络
作者
David Piatka,Raphaela L. Nánási,Ricky Mwangada Mwanake,Florian Engelsberger,Georg Willibald,Frank Neidl,Ralf Kiese
出处
期刊:Frontiers in water [Frontiers Media]
卷期号:5 被引量:7
标识
DOI:10.3389/frwa.2023.1321137
摘要

Stream ecosystems are actively involved in the biogeochemical cycling of carbon (C) and nitrogen (N) from terrestrial and aquatic sources. Streams hydrologically connected to peatland soils are suggested to receive significant quantities of particulate, dissolved, and gaseous C and N species, which directly enhance losses of greenhouse gases (GHGs), i.e., carbon dioxide (CO 2 ), methane (CH 4 ), and nitrous oxide (N 2 O), and fuel in-stream GHG production. However, riverine GHG concentrations and emissions are highly dynamic due to temporally and spatially variable hydrological, meteorological, and biogeochemical conditions. In this study, we present a complete GHG monitoring system in a peatland stream, which can continuously measure dissolved GHG concentrations and allows to infer gaseous fluxes between the stream and the atmosphere and discuss the results from March 31 to August 25 at variable hydrological conditions during a cool spring and warm summer period. Stream water was continuously pumped into a water-air equilibration chamber, with the equilibrated and actively dried gas phase being measured with two GHG analyzers for CO 2 and N 2 O and CH 4 based on Off-Axis Integrated Cavity Output Spectroscopy (OA-ICOS) and Non-Dispersive Infra-Red (NDIR) spectroscopy, respectively. GHG measurements were performed continuously with only shorter measurement interruptions, mostly following a regular maintenance program. The results showed strong dynamics of GHGs with hourly mean concentrations up to 9959.1, 1478.6, and 9.9 parts per million (ppm) and emissions up to 313.89, 1.17, and 0.40 mg C or N m −2 h −1 for CO 2 , CH 4 , and N 2 O, respectively. Significantly higher GHG concentrations and emissions were observed shortly after intense precipitation events at increasing stream water levels, contributing 59% to the total GHG budget of 762.2 g m −2 CO 2 -equivalents (CO 2 -eq). The GHG data indicated a constantly strong terrestrial signal from peatland pore waters, with high concentrations of dissolved GHGs being flushed into the stream water after precipitation. During drier periods, CO 2 and CH 4 dynamics were strongly influenced by in-stream metabolism. Continuous and high-frequency GHG data are needed to assess short- and long-term dynamics in stream ecosystems and for improved source partitioning between in-situ and ex-situ production.

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