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Dep. of Soil Science, Univ. of Alberta, Edmonton, Alberta, Canada T6G 2E3 and Centre for Land and Biological Resources Research (CLBRR), Agriculture Canada, Ottawa, Ontario, Canada
* Corresponding author (rgrant.gpu.srv.ualberta.ca).
ABSTRACT
If ecosystem simulation models are to be used to study changes in C distribution under proposed changes in climate, then they must represent the effects of soil physical conditions upon microbial activity. Hypotheses for the effects of soil water content (
) and temperature (Ts) on microbial oxidation rates were formulated into mathematical algorithms as part of the ecosys modelling program. Access to organic substrates by heterotrophic microbial populations was represented from competitive enzyme kinetics, which were presumed to be sensitive to
. Access to O2 by obligately aerobic or facultatively anaerobic microbial populations was represented from O2 diffusion gradients and active uptake rates controlled by
and Ts. Sensitivity to Ts of substrate hydrolysis and oxidation by heterotrophic microbial populations was modelled from an Arrhenius function. Rates of simulated respiration were tested against rates measured under laboratory and field conditions at different
and Ts. Simulated CO2 fluxes were largest when
= 0.6 to 0.7 of total porosity and declined to <0.2 of their largest values when
declined to 0.2 or rose above 0.9 of total porosity. The sensitivity of simulated CO2 fluxes to
was consistent with that measured during laboratory incubations, except in the range of 0.65 to 0.80 of total porosity, where sensitivity of measured fluxes was greater than that simulated. When
was >0.8 of total porosity, simulated respiratory quotients rose above 1.0 to values consistent with those recorded elsewhere at high
. Model hypotheses allowed simulated CO2 evolution rates to reproduce those reported from wheat residue during a 30-d incubation at Ts from 0 to 20°C and
s from –0.033 to –5.0 MPa. These hypotheses also allowed simulated changes in CO2 evolution rates attributed to changes in Ts and
to reproduce those measured in the field during 60 d under barley.
K1A 0C6. CLBRR Contribution no. 94-57.
Received for publication September 7, 1993.
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