Search for: All records

Permafrost sediments contain one of the largest reservoirs of organic carbon on Earth that is relatively stable when it remains frozen. As air temperatures increase, the shallow permafrost thaws which allows this organic matter to be converted into potent greenhouse gases such as methane (CH4) and carbon dioxide (CO2) through microbial processes. Along the Beaufort Sea coast in the vicinity of the Tuktoyaktuk Peninsula, Northwest Territories, Canada, warming air temperatures are causing the active layer above permafrost to deepen, and a number of active periglacial processes are causing rapid erosion of previously frozen permafrost. In this paper, we consider the biogeochemical consequences of these processes on the permafrost sediments found at Tuktoyaktuk Island. Our goals were to document the in situ carbon characteristics which can support microbial activity, and then consider rates of such activity if the permafrost material were to warm even further. Samples were collected from a 12mpermafrost core positioned on the top of the island adjacent to an eroding coastal bluff. Downcore CH4, total organic carbon and dissolved organic carbon (DOC) concentrations and stable carbon isotopes revealed variable in situ CH4 concentrations down core with a sub-surface peak just below the current active layer. The highest DOC concentrations were observed in the active layer. Controlled incubations of sediment from various depths were carried out from several depths anaerobically under thawed (5°C and 15°C) and under frozen (−20°C and −5°C) conditions. These incubations resulted in gross production rates of CH4 and CO2 that increased upon thawing, as expected, but also showed appreciable production rates under frozen conditions. This dataset presents the potential for sediments below the active layer to produce potent greenhouse gases, even under frozen conditions, which could be an important atmospheric source in the actively eroding coastal zone even prior to thawing. 

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.