Lakes are conduits of greenhouse gases to the atmosphere; however, most efflux estimates for individual lakes are based on extrapolations from a limited number of locations. Within‐lake variability in carbon dioxide (CO2) and methane (CH4) arises from differences in water sources, mixing, atmospheric exchange, and biogeochemical transformations, all of which vary across multiple temporal and spatial scales. We asked, how variable are CO2and CH4across the surface of a single lake, how do spatial patterns change seasonally, and how well does the typical sampling location represent the entire lake surface? During the 2016 ice‐free period, we mapped surface water concentrations of CO2and CH4approximately weekly in Lake Mendota (USA) and modeled diffusive gas exchange. During stratification, CO2was generally lower than atmospheric saturation (mean 19.81 μM) and relatively homogenous (mean coefficient of variation 0.12), whereas CH4was routinely extremely supersaturated (mean 0.29 μM) with greater spatial heterogeneity (mean coefficient of variation 0.65). During fall mixis, concentrations of both gases increased and became more spatially variable, but their spatial arrangements differed. In this system, samples collected from the lake center reasonably well represented the spatially weighted mean CO2concentration but overestimated annual CO2efflux by 21%. For CH4, the lake center underestimated annual diffusive efflux by only 8.6% but poorly represented lakewide concentrations and fluxes on any given day. Upscaling from a single site to the whole lake requires consideration of spatial variation to assess lakewide carbon dynamics due to heterogeneity in within‐lake processing, transport to the lake surface, and exchange with the atmosphere.
Seasonally ice‐covered permafrost lakes in the Arctic emit methane to the atmosphere during periods of open‐water. However, processes contributing to methane cycling under‐ice have not been thoroughly addressed despite the potential for significant methane emission to the atmosphere at ice‐out. We studied annual dissolved methane dynamics within a small (0.2 ha) Mackenzie River Delta lake using sensor and water sampling packages that autonomously and continuously collected lake water samples, respectively, for two years at multiple water column depths. Lake physical and biogeochemical properties (temperature; light; concentrations of dissolved oxygen, manganese, iron, and dissolved methane, including stable carbon, and radiocarbon isotopes) revealed annual patterns. Dissolved methane concentrations increase under‐ice after electron acceptors (oxygen, manganese, and iron oxides) are depleted or inaccessible from the water column. The radiocarbon age of dissolved methane suggests a source from recently decomposed carbon as opposed to thawed ancient permafrost. Sources of dissolved methane under‐ice include a diffusive flux from the sediments and may include water column methanogenesis and/or under‐ice hydrodynamic controls. Following ice‐out, the water column only partially mixes allowing half of the winter‐derived dissolved methane to be microbially oxidized. Despite oxidation at depth, surface water was a source of methane to the atmosphere. The greatest diffusive fluxes to the atmosphere occurred following ice‐out (75 mmol CH4m−2 d−1) and during a mixing episode in mid‐July, likely driven by a storm event. This study demonstrates the importance of fine‐scale temporal sampling to understand dissolved methane processes in seasonally ice‐covered lakes.
more » « less- NSF-PAR ID:
- 10445091
- Publisher / Repository:
- DOI PREFIX: 10.1029
- Date Published:
- Journal Name:
- Journal of Geophysical Research: Biogeosciences
- Volume:
- 126
- Issue:
- 3
- ISSN:
- 2169-8953
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
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