Tm. Hoehler et al., FIELD AND LABORATORY STUDIES OF METHANE OXIDATION IN AN ANOXIC MARINESEDIMENT - EVIDENCE FOR A METHANOGEN-SULFATE REDUCER CONSORTIUM, Global biogeochemical cycles, 8(4), 1994, pp. 451-463
Field and laboratory studies of anoxic sediments from Cape Lookout Big
ht, North Carolina, suggest that anaerobic methane oxidation is mediat
ed by a consortium of methanogenic and sulfate-reducing bacteria. A se
asonal survey of methane oxidation and CO2 reduction rates indicates t
hat methane production was confined to sulfate-depleted sediments at a
ll times of year, while methane oxidation occurred in two modes. In th
e summer, methane oxidation was confined to sulfate-depleted sediments
and occurred at rates lower than those of CO2 reduction. In the winte
r, net methane oxidation occurred in an interval at the base of the su
lfate-containing zone. Sediment incubation experiments suggest both me
thanogens and sulfate reducers were responsible for the observed metha
ne oxidation. In one incubation experiment both modes of oxidation wer
e partially inhibited by 2-bromoethanesulfonic acid (a specific inhibi
tor of methanogens). This evidence, along with the apparent confinemen
t of methane oxidation to sulfate-depleted sediments in the summer, in
dicates that methanogenic bacteria are involved in methane oxidation.
In a second incubation experiment, net methane oxidation was induced b
y adding sulfate to homogenized methanogenic sediments, suggesting tha
t sulfate reducers also play a role in the process. We hypothesize tha
t methanogens oxidize methane and produce hydrogen via a reversal of C
O2 reduction. The hydrogen is efficiently removed and maintained at lo
w concentrations by sulfate reducers. Pore water Hz concentrations in
the sediment incubation experiments (while net methane oxidation was o
ccurring) were low enough that methanogenic bacteria could derive suff
icient energy for growth from the oxidation of methane. The methanogen
-sulfate reducer consortium is consistent not only with the results of
this study, but may also be a feasible mechanism for previously docum
ented anaerobic methane oxidation in both freshwater and marine enviro
nments.