期刊
EUROPEAN JOURNAL OF SOIL SCIENCE
卷 55, 期 1, 页码 63-69出版社
WILEY-BLACKWELL
DOI: 10.1046/j.1365-2389.2004.00588.x
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Isotopically exchanged phosphorus is difficult to determine in soils that strongly sorb P (so that there is little P in solution) and in soils with large concentrations of colloidal P in soil suspensions. A method is proposed in which anion exchange membranes (AEM) are added to the soil suspension after an initial period of isotopic exchange with P-32-labelled phosphate ions. Isotopically exchanged P, termed E-AEM, is calculated from the ratio of labelled phosphate ions to the total phosphate ions on the membrane. The E-AEM was compared with the E value measured in an aqueous soil extract (E-Water extract) for 14 soils with different degrees of P sorption. The two methods gave similar results in soils with large P concentrations in an aqueous soil extract. However, E-Water extract values significantly exceeded the E-AEM values by up to 18-fold when soluble P was near the determination limit (0.008 mg P l(-1)). In a second experiment, two Ferralsols received further P from inorganic and plant sources and were incubated for 7 days. Treatment effects on labile P were erroneous as detected by the E-Water extract but were significant as detected with the AEM method. Third, E-AEM values were followed in a Lixisol and a Ferralsol which received labelled phosphate ions with carrier just before the beginning of a 23-day incubation. The approximate recovery of added inorganic P in the E-AEM value suggested that this method adequately samples labile P in P-sorbing soils. All these results showed that errors in the determination of E values for soils with very small concentrations of P in the soil solution are reduced using the proposed method.
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