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Urban landscapes and legacy industry provide hotspots for riverine greenhouse gases: A source-to-sea study of the River Clyde.
- Source :
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Water Research . Jun2023, Vol. 236, pN.PAG-N.PAG. 1p. - Publication Year :
- 2023
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Abstract
- • Urban wastewater, mine water and agricultural inputs dominated GHG generation. • Anthropogenic urban nutrient sources disproportionality increased GHGs in summer. • Low oxygen and high riverine residence time increased nutrient impacts on GHGs. • A source-to sea methodology enabled easy identification of GHG sources and sinks. • Load appointment modelling enabled separation of point and diffuse GHG sources. There is growing global concern that greenhouse gas (GHG) emissions from water bodies are increasing because of interactions between nutrient levels and climate warming. This paper investigates key land-cover, seasonal and hydrological controls of GHGs by comparison of the semi-natural, agricultural and urban environments in a detailed source-to-sea study of the River Clyde, Scotland. Riverine GHG concentrations were consistently oversaturated with respect to the atmosphere. High riverine concentrations of methane (CH 4) were primarily associated with point source inflows from urban wastewater treatment, abandoned coal mines and lakes, with CH 4 -C concentrations between 0.1 - 44 µg l−1. Concentrations of carbon dioxide (CO 2) and nitrous oxide (N 2 O) were mainly driven by nitrogen concentrations, dominated by diffuse agricultural inputs in the upper catchment and supplemented by point source inputs from urban wastewater in the lower urban catchment, with CO 2 -C concentrations between 0.1 - 2.6 mg l−1 and N 2 O-N concentrations between 0.3 - 3.4 µg l−1. A significant and disproportionate increase in all GHGs occurred in the lower urban riverine environment in the summer, compared to the semi-natural environment, where GHG concentrations were higher in winter. This increase and change in GHG seasonal patterns points to anthropogenic impacts on microbial communities. The loss of total dissolved carbon, to the estuary is approximately 48.4 ± 3.6 Gg C yr−1, with the annual inorganic carbon export approximately double that of organic carbon and four times that of CO 2, with CH 4 accounting for 0.03%, with the anthropogenic impact of disused coal mines accelerating DIC loss. The annual loss of total dissolved nitrogen to the estuary is approximately 4.03 ± 0.38 Gg N yr−1 of which N 2 O represents 0.06%. This study improves our understanding of riverine GHG generation and dynamics which can contribute to our knowledge of their release to the atmosphere. It identifies where action could support reductions in aquatic GHG generation and emission. [Display omitted] [ABSTRACT FROM AUTHOR]
Details
- Language :
- English
- ISSN :
- 00431354
- Volume :
- 236
- Database :
- Academic Search Index
- Journal :
- Water Research
- Publication Type :
- Academic Journal
- Accession number :
- 163388128
- Full Text :
- https://doi.org/10.1016/j.watres.2023.119969