Effect of lithological substrate on microbial biomass and enzyme activity in brown soil profiles in the northern Apennines (Italy)

The aim of the present study was to investigate the microbial activity along forest brown soil profiles sequence developed on different lithological substrates (carbonate or non-carbonated cement in sandstone formations) at different altitudes. The main question posed was: does carbonate affect the biochemical activity of brown soil profiles at different altitudes? For the purpose of this study, four soil profiles with different amounts and compositions of SOM developed on different lithological substrates were selected: two with carbonate (MB and MZ) and the other two with non-carbonated cement in the sandstone formations (MF1 and MF2). Chemical and biochemical properties of soil were analysed along soil profiles in order to assess the SOM quantity and quality, namely total organic C (C_org), water extractable organic C (WEOC) and humification indices (HI, DH, HR). Microbial biomass (C_mic and N_mic) content, as well as the specific activities of acid phosphatase, β-glucosidase and chitinase enzymes were chosen as indicators of biochemical activity. The soil biochemical properties provided evidence of better conditions for microorganisms in MB than in MF1, MF2 and MZ soil profiles, since patterns of microbial biomass content and activity might be expected in response to the amount and quality of organic substances. The different lithological substrates did not show any clear effect on soil microbial biomass content, since similar values were obtained in MF1, MF2 (with non-carbonated cement) and MZ (with carbonate). However, the specific activities of acid phosphatase (per unit of C_org and per unit of C_mic) were higher in soils with no carbonate (MF1 and MF2) than in soils with carbonate (MB and MZ). In conclusion, the biochemical activity along brown soil profiles was mainly regulated by different soil organic matter content and quality, while the two different lithological substrates (with carbonate or non-carbonated cement in the sandstone formations) did not show any direct effect on microbial biomass and its activity. However, the activity of acid phosphatase per unit of C was particularly enhanced in soil with non-carbonate cement in the sandstone formations.     

Determination of the fate of regularly applied 13C‐labeled‐artificial‐exudates C in two agricultural soils

Exudates are part of the total rhizodeposition released by plant roots to soil and are considered as a substantial input of soil organic matter. Exact quantitative data concerning the contribution of exudates to soil C pools are still missing. This study was conducted to reveal effects of ¹³C‐labeled exudate (artificial mixture) which was regularly applied to upper soil material from two agricultural soils. The contribution of exudate C to water‐extractable organic C (WEOC), microbial biomass C (MBC), and CO₂‐C evolution was investigated during a 74 d incubation. The WEOC, MBC, and CO₂‐C concentrations and the respective δ¹³C values were determined regularly. In both soils, significant incorporation of artificial‐exudate‐derived C was observed in the WEOC and MBC pool and in CO₂‐C. Up to approx. 50% of the exudate‐C amounts added were recovered in the order WEOC << MBC < CO₂‐C in both soils at the end of the incubation. Newly built microbial biomass consisted mainly of exudates, which substituted soil‐derived C. Correspondingly, the CO₂‐C evolved from exudate‐treated soils relative to the controls was dominated by exudate C, showing a preferential mineralization of this substrate. Our results suggest that the remaining 50% of the exudate C added became stabilized in non‐water‐extractable organic fractions. This assumption was supported by the determination of the total organic C in the soils on the second‐last sampling towards the end of the incubation. In the exudate‐treated soils, significantly more soil‐derived C compared to the controls was found in the WEOC on almost all samplings and in the MBC on the first sampling. This material might have derived from exchange processes between the added exudate and the soil matrix. This study showed that easily available substrates can be stabilized in soil at least in the short term.     

Spatial and temporal patterns of water-extractable organic carbon (WEOC) of surface mineral soil in a cool temperate forest ecosystem

Water-extractable organic carbon (WEOC) drives the C and N cycles in forest ecosystems via microbial activity. However, few studies have considered both then spatial and temporal patterns of WEOC in forest soils. We investigated the spatial and temporal variation in WEOC along a topographic sequence in a cool temperate deciduous forest. The concentrations of WEOC, carbohydrates, total phenols, and other organics were 126±51, 40±15, 1.5±0.5 and 85±43 mg C kg dry soil⁻¹, respectively. Carbohydrates and phenols accounted for 33±11 and 1.5±1.0% of WEOC, respectively. The effect of season on the WEOC concentration was stronger than that of slope position the growing season, although most of the soil properties varied markedly with slope position. The concentration of carbohydrates in WEOC showed similar seasonal patterns across slope positions. The carbohydrate concentration peaked in May and August. The results suggest that carbohydrates are controlled by the recent production of C, rather than by organic C that has accumulated in soil.     

Determination of the fate of C labelled maize and wheat rhizodeposit-C in two agricultural soils in a greenhouse experiment under C-CO2-enriched atmosphere

A deeper understanding of the contribution of carbon (C) released by plant roots (rhizodeposition) to soil organic matter (SOM) can help to increase our knowledge of global C-cycling. These insights can eventually lead to sustainable management of SOM especially in agricultural systems. This study was conducted to determine the fate of ¹³C labelled rhizodeposit-C of maize and wheat plants. They were grown in a greenhouse in permeable nylon bags filled with upper soil material from two agricultural soils of the same location, but with different crop yields. The bags were placed into pots, which were also filled with soil surrounding the bags. Soil inside the bags was considered as rhizosphere soil, wheras the one outside the bags represented bulk soil. The contributions of rhizodeposits to water extractable organic carbon (WEOC), microbial biomass-C (MB-C), CO₂-C evolution, and total organic carbon (C_org) were investigated during a 7-week growing period. The WEOC, MB-C, CO₂-C, C_org contents and the respective δ¹³C values were determined regularly, and a newly developed method for determining δ¹³C values in soil extracts was applied.In both soils, regardless of crop yield potential, significant incorporation of rhizodeposition-derived C was observed in the MB-C, CO₂-C, and C_org pool, but not in the WEOC. The pattern of C incorporation into the different pools was the same for both soils with both plants, and rhizodeposit-derived C was recovered in the order MB-C<C_org<CO₂-C. This showed that rhizodeposits were mainly respired, but since C_org was the second largest pool of the overall balances, they were also stabilized in the soils at least in the short term. It is suggested that the increased SOM mineralization observed in this study (positive priming effects) was probably induced by C exchange processes between the soil matrix and soluble rhizodeposits. Moreover, soluble rhizodeposit-C was detected in MB-C and CO₂-C evolved outside the direct root zone, showing the availability of these C-components in the bulk soil.