Organo-mineral associations in sandy acid forest soils: importance of specific surface area, iron oxides and micropores

Organo-mineral associations stabilize soil organic matter, though the mechanisms by which they do so are unclear. We used particle-size fractions < 6.3 μm of two soils to examine the importance of Fe oxides, short-range order Al silicates and the surface areas of minerals and micropores on the formation of organo-mineral associations. In the subsoil Fe oxides were most strongly statistically correlated with the mineral-bound organic carbon. We therefore assume that they are the most important substrates for the formation of organo-mineral associations. There is no indication that this is caused by physical protection of organic matter in their micropores (< 2 nm). In the Haplic Podzol, dithionite–citrate–bicarbonate-soluble short-range order Al silicates may also play a role. Fe oxide particles were calculated to offer specific surface areas of ～ 200 m² g^?1 (goethite) and ～ 800 m² g^?1 (ferrihydrite), corresponding to crystal diameters of only a few nm. We assume that the resulting large amount of oxide-specific reactive surface sites (conditionally charged hydroxyl groups) is responsible for their dominant role as sorbents. With maximum C loadings of 1.3 mg C per m² Fe oxide for the Dystric Cambisol and 1.1 mg C per m² Fe oxide + short-range order Al silicates for the Haplic Podzol the subsoils of both soils seem to have reached saturation with respect to organic matter sorption. In contrast to subsoil horizons, organo-mineral associations from topsoils contain much larger amounts of organic matter. Here a larger C loading on Fe oxides or a greater importance of other sorbents in addition to the oxides must be assumed.