Ws. Reeburgh et al., CARBON KINETIC ISOTOPE EFFECT ACCOMPANYING MICROBIAL OXIDATION OF METHANE IN BOREAL FOREST SOILS, Geochimica et cosmochimica acta, 61(22), 1997, pp. 4761-4767
Atmospheric methane (CH4) oxidation occurs in soils at sites in the Bo
nanza Creek L.T.E.R. near Fairbanks, Alaska, USA, at rates less than o
r equal to 2 mg CH4 m(-2) d(-1); the maximum CH4 oxidizing activity is
located in loess at a depth of similar to 15 cm. Methane, carbon diox
ide, and stable isotope (delta(13)C-CH4, delta(13)C-CO2) depth distrib
utions were measured at two sites: South facing Aspen (AS2) and North
facing Black Spruce (BS2). The combined effects of diffusion and oxida
tion are similar at both sites and result in a CH4 concentration decre
ase (1.8-0.1 ppm) and a delta(13)C-CH4 increase (-48 parts per thousan
d to -43 parts per thousand) from the soil surface to 60-80 cm depth.
Isotope flux ratio and diffusion-consumption models were used to estim
ate the kinetic isotope effect (KIE); these results agree with the obs
erved top-to-bottom difference in delta(13)C-CH4, which is the integra
ted result of isotope fractionation due to diffusion and oxidation. Th
e KIE for CH, oxidation determined from these measurements is 1.022-1.
025, which agrees with previous KIE determinations based on changes in
headspace CH4 concentration and delta(13)C-CH4 over time. A much lowe
r soil respiration rate in the North facing Black Spruce soils is indi
cated by fivefold lower soil CO2 concentrations. The similarity in CH4
oxidation at the two sites and the differences in inferred soil respi
ration at the two sites suggest that soil CH4 oxidation and soil respi
ration are independent processes. The soil organic matter responsible
for the CO2 flux has a delta(13)C estimated to be -27 to -28 parts per
thousand. Copyright (C) 1997 Elsevier Science Ltd.