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that different types of plant material lead to different rates of acetate formation.
There is also a stronger substrate-based coupling of root surface and methanogens
in oligotrophic (bog) than in minerotrophic (fen) sites (Cadillo-Quiroz et al. 2010 ;
Ström et al. 2003 ; Öquist and Svensson 2002 ). Seasonal algal or phytoplankton
blooms might be responsible for formation of acetate and CH 4 in the sediments
of deep lakes (Schulz and Conrad 1995 ). The acetate concentration profiles show
maxima (~100 μ M in 2 or 4 cm depth) in summer and minima (~5 μ M over the
entire depth) in winter, when the respective CH 4 concentrations are ~750 μ M in
summer and ~120 μ M in winter (Schulz and Conrad 1995 ).
It is evidenced that gas bubbles contain about 60-70 % CH 4 with an average
δ 13 C of -56.2 % and δ D of -354 %, and 2 % CO 2 with an average δ 13 C of -14.1 %
(Thebrath et al. 1993 ). These data indicate that CH 4 is produced from methyl car-
bon, i.e. mainly using acetate as fermentative substrate (Thebrath et al. 1993 ).
In anoxic paddy soil, interspecies H 2 transfer within methanogenic bacterial asso-
ciations (MBA) account for 95-97 % of the conversion of 14 CO 2 to 14 CH 4 , and
only 3-5 % of the 14 CH 4 is produced from the turnover of dissolved H 2 (Conrad
et al. 1989a , b ). An experimental study demonstrates that the ratio of Fe(II) pro-
duction to CO 2 production (3.9) is similar to that expected (4.0) for organic carbon
oxidation coupled to Fe(III) oxide reduction (Fig. 8 ) (Roden and Wetzel 1996 ).
The study also shows that the rates of CH 4 production are low during the Fe(III)
reduction in oxidized sediments, but increase when the Fe(III) oxides are depleted
to background levels (Fig. 8 a). The rates of CO 2 and CH 4 production are about
Fig. 8 Fe(III) reduction, CO 2 production, and CH 4 production in oxidized ( a , b ) and reduced ( c ,
d ) Talladega wetland sediment slurries. Data source Roden and Wetzel ( 1996 )
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