Increases in soil P availability due to liming have been reported in a numb
er of glasshouse and field trials, but the mechanism responsible for this e
ffect has not been identified definitely. In a laboratory study, we examine
d the effects of lime on labile P fractions in six New Zealand soils that v
aried in P-retention capacity. The soils (5.1-5.5 initial pH in water) were
incubated with four rates of CaCO3 to raise pH incrementally to a maximum
of approximate to6.5. Snbsequently, P las KH2PO4) was applied to give three
P levels in each soil. Liming generally decreased Olsen bicarbonate values
, with the effect being largest at the highest rate of P addition. Averaged
across P treatments, the decrease in Olsen P for a unit increase in pH ran
ged from 3 to 7 mg kg(-1). Liming also tended to depress water-extractable
P, Decreases in extractable P suggest that liming increased phosphate adsor
ption. When data for the lime and P treatments were combined, water-extract
able P and Olsen P were well correlated, although each soil showed a differ
ent relationship. Phosphate retention capacity appeared to have a strong in
fluence on tile relationship between water-extractable P and Olsen P, with
the high P retention soils having relatively low proportions of water-extra
ctable P. When exchangeable cations were replaced with Na, soils that had b
een limed released significantly more P to distilled water than their unlim
ed counterparts. The results confirm that the nature of the exchangeable ca
tion suite has a major influence on the pa-dependence of the phosphate adso
rption-desorption equilibrium. In limed soil, exchangeable Ca and pH increa
se simultaneously so that shifts in this equilibrium may be small and unpre
dictable.