Abstract

SUMMARYThe significance of exchangeable cations in the release of phosphorus by sequential extraction with water was evaluated in 11 acid (pH 5.0–6.3) New Zealand soils contrasting in P status and P retention. The release of P from Na‐saturated soil exceeded that from the original Ca‐dominated soils by up to four‐fold. Possible explanations for the larger P release in the Na system include: (i) desorption of P induced by increased surface negative potential associated with the exchange of Na for Ca/Mg, and/or (ii) accelerated dissolution of Ca phosphate compounds or complexes resulting from the creation of a sink for Ca.The potential of a series of anion‐ and cation‐exchange resin systems (AER and CER, respectively) as sinks for labile soil P was also examined. For all soils studied, P extracted by AER‐HCO3 <AER‐OH/CER‐Na< AER‐OH/CER‐H. The success of the AER‐OH/ CER‐H system in extracting P is attributed to its ability to remove exchangeable Ca and Mg, and to reduce the ionic strength of the equilibrating solution. A high correlation (r= 0.99**) was obtained between P extracted by AER‐HCO3 and that removed by sequential extraction with water. Also, the amounts of P extracted by AER‐OH/CER‐H and NaCl/ H2O were closely correlated (r= 0.95**), suggesting similar release mechanisms. The results obtained indicate that charge‐balancing cations, particularly Ca which is the predominant exchangeable cation in the majority of soils, exerts a more significant control on soil P equilibria in acid soils than is commonly recognized.

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