Temperature sensitivity of soil enzymes along an elevation gradient in the Peruvian Andes

Soil enzymes are catalysts of organic matter depolymerisation, which is of critical importance for ecosystem carbon (C) cycling. Better understanding of the sensitivity of enzymes to temperature will enable improved predictions of climate change impacts on soil C stocks. These impacts may be especially large in tropical montane forests, which contain large amounts of soil C. We determined the temperature sensitivity (Q 10) of a range of hydrolytic and oxidative enzymes involved in organic matter cycling from soils along a 1900 m elevation gradient (a 10 °C mean annual temperature gradient) of tropical montane forest in the Peruvian Andes. We investigated whether the activity (V max) of selected enzymes: (i) exhibited a Q 10 that varied with elevation and/or soil properties; and (ii) varied among enzymes and according to the complexity of the target substrate for C-degrading enzymes. The Q 10 of V max for β-glucosidase and β-xylanase increased with increasing elevation and declining mean annual temperature. For all other enzymes, including cellobiohydrolase, N-acetyl β-glucosaminidase and phosphomonoesterase, the Q 10 of V max did not vary linearly with elevation. Hydrolytic enzymes that degrade more complex C compounds had a greater Q 10 of V max, but this pattern did not apply to oxidative enzymes because phenol oxidase had the lowest Q 10 value of all enzymes studied here. Our findings suggest that regional differences in the temperature sensitivities of different enzyme classes may influence the terrestrial C cycle under future climate warming

Drying and substrate concentrations interact to inhibit decomposition of carbon substrates added to combusted Inceptisols from a boreal forest

Climate change is expected to alter the mechanisms controlling soil organic matter (SOM) stabilization. Under climate change, soil warming and drying could affect the enzymatic mechanisms that control SOM turnover and dependence on substrate concentration. Here, we used a greenhouse climate manipulation in a mature boreal forest soil to test two specific hypotheses: (1) Rates of decomposition decline at lower substrate concentrations, and (2) reductions in soil moisture disproportionately constrain the degradation of low-concentration substrates. Using constructed soil cores, we measured decomposition rates of two polymeric substrates, starch and cellulose, as well as enzyme activities associated with degradation of these substrates. The greenhouse manipulation increased temperature by 0.8 °C and reduced moisture in the constructed cores by up to 90 %. We rejected our first hypothesis, as the rate of starch decomposition did not decrease with declining starch concentration under control conditions, but we did find support for hypothesis two: Drying led to lower decomposition rates for low-concentration starch. We observed a threefold reduction in soil respiration rates in bulk soils in the greenhouses over a 4-month period, but the C losses from the constructed cores did not vary among our treatments. Activities of enzymes that degrade cellulose and starch were elevated in the greenhouse treatments, which may have compensated for moisture constraints on the degradation of the common substrate (i.e., cellulose) in our constructed cores. This study confirms that substrate decomposition can be concentration-dependent and suggests that climate change effects on soil moisture could reduce rates of decomposition in well-drained boreal forest soils lacking permafrost