Abstract
Current methods for determining inorganic sulphur (S) in aerated mineral soil horizons often result in underestimates. To overcome this defect we developed a new method combining a batch extraction with 0.5 M NH 4 F solution at a soil:solution ratio of 1:5 with a subsequent analysis of the mobilized SO 4 2- by ion chromatography. The ammonium fluoride extraction enables us to characterize inorganic sulphate in non-calcareous forest soils. It is more efficient than conventional procedures in which inorganic S is extracted with phosphate or bicarbonate solution. In contrast to the extraction with strongly alkaline reagents (NaOH, KOH, LiOH), the NH 4 + -NH 3 buffer system in NH4F prevents the pH of the suspension from exceeding 9.0 and thus the undesired conversion of organic S into SO 4 2- by auto-oxidation and hydrolysis of ester sulphate. In a comparison we demonstrated that the inorganic S in six German forest soils is underestimated by up to 50% or 200 kg S ha -1 in the uppermost 60cm, if it is assessed by extraction with 0.016 M KH 2 PO 4 or 0.5 M NaHCO 3 instead of 0.5 M NH 4 F. Conversely, the pool of ester sulphate is overestimated almost threefold.
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