Abstract

Abstract. Marine microbial communities can consume dissolved methane before it can escape to the atmosphere and contribute to global warming. Seawater over the shallow Arctic shelf is characterized by excess methane compared to atmospheric equilibrium. This methane originates in sediment, permafrost, and hydrate. Particularly high concentrations are found beneath sea ice. We studied the structure and methane oxidation potential of the microbial communities from seawater collected close to Utqiagvik, Alaska, in April 2016. The in situ methane concentrations were 16.3 ± 7.2 nmol L−1, approximately 4.8 times oversaturated relative to atmospheric equilibrium. The group of methane-oxidizing bacteria (MOB) in the natural seawater and incubated seawater was > 97 % dominated by Methylococcales (γ-Proteobacteria). Incubations of seawater under a range of methane concentrations led to loss of diversity in the bacterial community. The abundance of MOB was low with maximal fractions of 2.5 % at 200 times elevated methane concentration, while sequence reads of non-MOB methylotrophs were 4 times more abundant than MOB in most incubations. The abundances of MOB as well as non-MOB methylotroph sequences correlated tightly with the rate constant (kox) for methane oxidation, indicating that non-MOB methylotrophs might be coupled to MOB and involved in community methane oxidation. In sea ice, where methane concentrations of 82 ± 35.8 nmol kg−1 were found, Methylobacterium (α-Proteobacteria) was the dominant MOB with a relative abundance of 80 %. Total MOB abundances were very low in sea ice, with maximal fractions found at the ice–snow interface (0.1 %), while non-MOB methylotrophs were present in abundances similar to natural seawater communities. The dissimilarities in MOB taxa, methane concentrations, and stable isotope ratios between the sea ice and water column point toward different methane dynamics in the two environments.

Highlights

  • Methane (CH4) is the third most abundant greenhouse gas contributing to climate change (IPCC, 2014) – exceeded only by water vapor and carbon dioxide

  • For most days during the sampling period, the water column at station ice mass balance buoy” (IMB) was characterized by temperatures around −1.8 ◦C and salinities of 33.9 to 36.4

  • We studied the structure and methane oxidation potential of microbial communities from Arctic seawater and sea ice

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Summary

Introduction

Methane (CH4) is the third most abundant greenhouse gas contributing to climate change (IPCC, 2014) – exceeded only by water vapor and carbon dioxide. The two major sources of methane are ongoing biogenic production by microbes in anoxic sediment (Formolo, 2010; Reeburgh, 2007; Whiticar, 1999) and release of fossil methane from geological storage (summarized by Kvenvolden and Rogers, 2005; Saunois et al, 2016). More than 90 % of the methane sourced in the seabed is oxidized within the sediment by anaerobic and aerobic oxidation (Barnes and Goldberg, 1976; Boetius and Wenzhöfer, 2013; Knittel and Boetius, 2009; Reeburgh, 1976). The remaining methane either diffuses into the water at the sediment surface or is released as bubbles, which completely or partially dissolve while rising through the water column (Leifer and Patro, 2002).

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