Open AccessWhat prevents outgassing of methane to the atmosphere in Lake Tanganyika?
Author(s) -
DurischKaiser Edith,
Schmid Martin,
Peeters Frank,
Kipfer Rolf,
Dinkel Christian,
Diem Torsten,
Schubert Carsten J.,
Wehrli Bernhard
Publication year - 2011
Publication title -
journal of geophysical research: biogeosciences
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.67
H-Index - 298
eISSN - 2156-2202
pISSN - 0148-0227
DOI - 10.1029/2010jg001323
Subject(s) - anoxic waters , water column , methane , environmental chemistry , anaerobic oxidation of methane , methanogenesis , biogeochemical cycle , organic matter , environmental science , epilimnion , hypolimnion , oceanography , eutrophication , geology , chemistry , ecology , biology , nutrient
Tropical East African Lake Tanganyika hosts the Earth's largest anoxic freshwater body. The entire water column holds over 23 Tg of the potent greenhouse gas methane (CH 4 ). Methane is formed under sulphate‐poor conditions via carbon dioxide reduction or fermentation from detritus and relict sediment organic matter. Permanent density stratification supports an accumulation of CH 4 below the permanent oxycline. Despite CH 4 significance for global climate, anaerobic microbial consumption of CH 4 in freshwater is poorly understood. Here we provide evidence for intense methanotrophic activity not only in the oxic but also in the anoxic part of the water column of Lake Tanganyika. We measured CH 4 , 13 C of dissolved CH 4 , dissolved oxygen (O 2 ), sulphate (SO 4 2− ), sulphide (HS − ) and the transient tracers chlorofluorocarbon‐12 (CFC‐12) and tritium ( 3 H). A basic one‐dimensional model, which considers vertical transport and biogeochemical fluxes and transformations, was used to interpret the vertical distribution of these substances. The results suggest that the anaerobic oxidation of CH 4 is an important mechanism limiting CH 4 to the anoxic zone of Lake Tanganyika. The important role of the anaerobic oxidation for CH 4 concentrations is further supported by high abundances (up to ∼33% of total DAPI‐stained cells) of single living archaea, identified by fluorescence in situ hybridization.