Lakes are a natural source of methane to the atmosphere and contribute significantly to total emissions compared to the oceans. Controls on methane emissions from lake surfaces, particularly biotic processes within anoxic hypolimnia, are only partially understood. Here we investigated biological methane oxidation in the water column of the seasonally stratified Lake Rotsee. A zone of methane oxidation extending from the oxic/anoxic interface into anoxic waters was identified by chemical profiling of oxygen, methane and δ13C of methane. Incubation experiments with 13C-methane yielded highest oxidation rates within the oxycline, and comparable rates were measured in anoxic waters. Despite predominantly anoxic conditions within the zone of methane oxidation, known groups of anaerobic methanotrophic archaea were conspicuously absent. Instead, aerobic gammaproteobacterial methanotrophs were identified as the active methane oxidizers. In addition, continuous oxidation and maximum rates always occurred under light conditions. These findings, along with the detection of chlorophyll a, suggest that aerobic methane oxidation is tightly coupled to light-dependent photosynthetic oxygen production both at the oxycline and in the anoxic bottom layer. It is likely that this interaction between oxygenic phototrophs and aerobic methanotrophs represents a widespread mechanism by which methane is oxidized in lake water, thus diminishing its release into the atmosphere.

Methane-oxidizing bacteria represent a major biological sink for methane and are thus Earth’s natural protection against this potent greenhouse gas. Here we show that in two stratified freshwater lakes a substantial part of upward-diffusing methane was oxidized by filamentous gamma-proteobacteria related to Crenothrix polyspora. These filamentous bacteria have been known as contaminants of drinking water supplies since 1870, but their role in the environmental methane removal has remained unclear. While oxidizing methane, these organisms were assigned an ‘unusual’ methane monooxygenase (MMO), which was only distantly related to ‘classical’ MMO of gamma-proteobacterial methanotrophs. We now correct this assignment and show that Crenothrix encode a typical gamma-proteobacterial PmoA. Stable isotope labeling in combination swith single-cell imaging mass spectrometry revealed methane-dependent growth of the lacustrine Crenothrix with oxygen as well as under oxygen-deficient conditions. Crenothrix genomes encoded pathways for the respiration of oxygen as well as for the reduction of nitrate to N2O. The observed abundance and planktonic growth of Crenothrix suggest that these methanotrophs can act as a relevant biological sink for methane in stratified lakes and should be considered in the context of environmental removal of methane.

Freshwater lakes represent a substantial natural source of methane to the atmosphere and thus contribute to global climate change. Microbial methane oxidation is an important control on methane release from these systems, where oxygen appears to be the most essential electron acceptor for this process. However, there is extensive geochemical evidence that methane is also oxidized under anoxic conditions in lakes, though the details about the exact mechanism have still not been resolved. Here, we investigated the fate of methane in the water column of meromictic Lake Zug. We provide evidence for ongoing methane oxidation at the oxic/anoxic boundary and also in the anoxic hypolimnion, both apparently mediated by aerobic methane‐oxidizing bacteria. Gammaproteobacterial methanotrophs (gamma‐MOB) dominated the indigenous methanotrophic community and were active under all investigated conditions—oxic, sub‐oxic and anoxic. Methane oxidation was stimulated by the additions of oxygen or iron and manganese oxides under anoxic conditions. In the latter case, trace amounts of oxygen may have still been required for methane activation, yet these findings indicate that gamma‐MOB in Lake Zug might be able to respire electron acceptors other than oxygen. We propose that gamma‐MOB are actively removing methane also in anoxic lake waters, thus contributing to methane mitigation from these habitats.