Abstract

Soil organic matter (SOM) has vital roles in the global carbon (C) cycle and the use of organic amendments (OAs) to maintain or improve SOM levels is a promising practice. However, the mechanisms underlying SOM stabilization in OA-amended soils remain insufficiently resolved. For more effective understanding on such issues, we examined soil samples from a long-term experimental plot (26–31 years) that included six treatments, namely, a chemical fertilizer (CF) alone (CF), a bark compost plus CF (BC + CF), a coffee residue compost plus CF (CRC + CF), a cattle manure compost plus CF (CMC + CF), and a cattle manure (CMC) or sewage sludge compost (SSC) alone at a higher application rate, using physical fractionation. In the fractionation, free particulate SOM (fSOM), free SOM occluded in aggregates (oSOM), and SOM weakly bound to minerals (wSOM; s.g. 1.6–2.0 g cm−3) and strongly (sSOM; s.g. >2.0 g cm−3) were separated and characterized using 13C nuclear magnetic resonance (NMR) along with OAs and bulk soil samples. The long-term OA applications enhanced the total C accumulation and the amount of C accumulated as oSOM, wSOM, and sSOM correlated positively with the total C content. The application of BC or CRC resulted in a greater accumulation of fSOM. Conversely, the continuous application of SSC or CMC, which has a high N content and a low C/N ratio, led to a greater accumulation of C, mainly as wSOM. Our findings suggest that both the quality and quantity of OAs control the forms of C that accumulate and this involves different mechanistic pathways. We suggest that the abundant alkyl C in the wSOM and sSOM fractions was SSC-derived SOM in the SSC soil while in the case of the CMC soil, this was due to the increased contribution of microbial-derived SOM.

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