Chemical stabilization of organic carbon pools in particle size fractions in no-till and meadow soils

The knowledge about the relevance of physical and chemical fractionation methods to soil organic carbon (SOC) stabilization mechanisms is fragmentary but needed to manage the SOC pool. Therefore, our objective was to compare the C contents of the particle size fractions coarse and fine sand, silt, and clay of the two uppermost horizons of a soil under three different management systems (meadow; no-till corn, NT; no-till corn with manure, NTm). The mineral composition was dominated by silt (48–60%). However, coarse sand and clay showed the highest enrichment of C compared to the bulk soil. In spite of an enrichment factor below 1, the high proportion of silt made this fraction the main C store. In the upper 30 cm, this fraction amounted to 27.1 Mg C ha⁻¹ in NTm and progressively less in NT (15.5 Mg C ha⁻¹), and meadow (14.9 Mg C ha⁻¹), representing 44%, 39%, and 39% of the total SOC pool, respectively. The C in the isolated particle size fractions was further investigated by an oxidizing treatment with Na₂S₂O₈ and a treatment with HF to solubilize the mineral phases. The pools of oxidizable C were comparable among particle size fractions and pedons, as indicated by Na₂S₂O₈ treatment. The pools of C preferentially associated with soil minerals were also comparable among pedons, as indicated by HF treatment. However, NTm stored the largest pool (12.6 Mg ha⁻¹) of mineral-associated C in 0–30 cm depth. The silt-associated and mineral-bound SOC pool in NTm was greater compared to NT due to increased organic matter (OM) input. Thus, the silt particle size fraction at the North Appalachian Experimental Watershed (NAEW) has the potential for SOC sequestration by stabilizing OM inputs. Mineralogical and molecular level analyses on a larger set of fractions obtained from entire rooted soil profiles are required, however, to compare the SOC sequestration capacity of the land uses.