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.
- NSF-PAR ID:
- 10031623
- Publisher / Repository:
- Wiley Blackwell (John Wiley & Sons)
- Date Published:
- Journal Name:
- Limnology and Oceanography: Methods
- Volume:
- 15
- Issue:
- 1
- ISSN:
- 1541-5856
- Page Range / eLocation ID:
- 103 to 115
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
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Abstract A chemoautotrophy maximum is present in many anoxic basins at the sulfidic layer's upper boundary, but the factors controlling this feature are poorly understood. In 13 of 31 cruises to the Cariaco Basin, particulate organic carbon (POC) was enriched in13C (δ13CPOCas high as −16‰) within the oxic/sulfidic transition compared to photic zone values (−23 to −26‰). During “heavy” cruises, fluxes of O2and [NO3−+ NO2−] to the oxic/sulfidic interface were significantly lower than during “light” cruises. Cruises with isotopically heavy POC were more common between 2013 and 2015 when suspended particles below the photic zone tended to be nitrogen rich compared to later cruises. Within the chemoautotrophic layer, nitrogen‐rich particles (molar ratio C/N< 10) were more likely to be13C‐enriched than nitrogen‐poor particles, implying that these inventories were dominated by living cells and fresh detritus rather than laterally transported or extensively decomposed detritus. During heavy cruises,13C enrichments persisted to 1,300 m, providing the first evidence of downward transport of chemoautotrophically produced POC. Dissolved inorganic carbon assimilation during heavy cruises (
n = 3) was faster and occurred deeper than during light cruises (n = 2). Metagenomics data from the chemoautotrophic layer during two cruises support prevalence of microorganisms carrying RuBisCO form II genes, which encode a carbon fixation enzyme that discriminates less against heavy isotopes than most other carbon fixation enzymes, and metatranscriptomics data indicate that higher expression of form II RuBisCO genes during the heavy cruises at depths where essential reactants coexist are responsible for the isotopically heavier POC.
