Abstract

Soil horizons below 30 cm depth contain about 60% of the organic carbon stored in soils. Although insight into the physical and chemical stabilization of soil organic matter (SOM) and into microbial community composition in these horizons is being gained, information on microbial functions of subsoil microbial communities and on associated microbially-mediated processes remains sparse. To identify possible controls on enzyme patterns, we correlated enzyme patterns with biotic and abiotic soil parameters, as well as with microbial community composition, estimated using phospholipid fatty acid profiles. Enzyme patterns (i.e. distance-matrixes calculated from these enzyme activities) were calculated from the activities of six extracellular enzymes (cellobiohydrolase, leucine-amino-peptidase, N-acetylglucosaminidase, chitotriosidase, phosphatase and phenoloxidase), which had been measured in soil samples from organic topsoil horizons, mineral topsoil horizons, and mineral subsoil horizons from seven ecosystems along a 1500 km latitudinal transect in Western Siberia. We found that hydrolytic enzyme activities decreased rapidly with depth, whereas oxidative enzyme activities in mineral horizons were as high as, or higher than in organic topsoil horizons. Enzyme patterns varied more strongly between ecosystems in mineral subsoil horizons than in organic topsoils. The enzyme patterns in topsoil horizons were correlated with SOM content (i.e., C and N content) and microbial community composition. In contrast, the enzyme patterns in mineral subsoil horizons were related to water content, soil pH and microbial community composition. The lack of correlation between enzyme patterns and SOM quantity in the mineral subsoils suggests that SOM chemistry, spatial separation or physical stabilization of SOM rather than SOM content might determine substrate availability for enzymatic breakdown. The correlation of microbial community composition and enzyme patterns in all horizons, suggests that microbial community composition shapes enzyme patterns and might act as a modifier for the usual dependency of decomposition rates on SOM content or C/N ratios.

Highlights

  • These factors are most likely responsible for the clear separation of enzyme patterns according to horizons (R2 1⁄4 0.66), which was stronger than the differences in enzyme patterns between sites (R2 1⁄4 0.14; Fig. 3), in our study

  • While hydrolytic enzyme activities generally decreased with depth, POX activities did not change from topsoil to subsoil (Fig. 1)

  • An explanation for this might be that the activity of hydrolytic enzymes is often directly related to soil organic matter (SOM) content (Sinsabaugh et al, 2008; Schnecker et al, 2014)

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Summary

Introduction

Soil pH, one of the factors often associated with enzyme activities (Sinsabaugh et al, 2008), changes with depth (Eilers et al, 2012). In addition to these direct influences on enzyme activities, the availability of substrate for enzymatic breakdown decreases with depth. While the main proportion of SOM in topsoils is plant derived material, SOM in subsoils is microbially transformed (Wallander et al, 2003). During this microbial transformation of SOM, carbon is lost, mainly as CO2, whereas most of the nitrogen (N) is recycled and remains in the system, resulting in lower C/N ratios of subsoil SOM (Rumpel and Ko€gel-Knabner, 2011)

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