Forest soils are an important sink for atmospheric CH4 but the contribution
of CH4 oxidation, production and transport to the overall CH4 flux is diff
icult to quantify. It is important to understand the role these processes p
lay in CH4 dynamics of forest soils, to enable prediction of how the size o
f this sink will respond to future environmental change. Methane oxidation,
production and transport were investigated for a temperate forest soil, pr
eviously shown to be a net CH4 consumer, to determine the extent to which p
hysical and biological processes contributed to the not flux. The sum of ox
idation rates for soil layers were significantly greater (P<0.05) than for
the intact soil cores from which the layers were taken. Combined with the i
mmediate inhibition Of CH4 uptake on waterlogging soils, the findings sugge
sted that soil CH4 diffusion was an important regulator of CH4 uptake. In s
upport of this, a subsurface maximum for CH4 oxidation was observed, but th
e exact depth of the maximum differed when rates were calculated on a mass
or on an areal basis. Markedly varying potential CH4 uptake activities betw
een soil cores were masked in intact core rates. Potential CH4 oxidation co
nformed well to Michaelis-Menten kinetics but V-max K-t and a(A)(O) values
varied with depth, suggesting different functional methanotrophic communiti
es were active in the profile, The presence of monophasic kinetics in fresh
soil could not be used to infer that the soil was exposed only to CH4 mixi
ng ratios atmospheric, as challenging soils with 20% CH4 in air did not ind
uce low-affinity oxidation kinetics. Atmospheric CH4 oxidation potentiaks e
xceeded production potentials by 10-220 times. The results show that the fo
rest soil CH4 flux was dominated by CH4 oxidation and transport, methanogen
esis played only a minor role. (C) 2001 Elsevier Science Ltd. All rights re
served.