The partitioning of adsorbed P between labile and non-labile pools by
soils is fundamental to the residual effect of fertilizer-P added to s
oils. The main objective of the study was to determine the partitionin
g of adsorbed P between the labile and non-labile phases by some bench
mark soils of northeast Brazil for which is little is known. Surface a
nd subsurface samples of several soils: Non-Calcic Brown soil and Plan
osol (Haplustalfs), Cambisol (Ustropept), Lithosols (Orthents) and All
uvial soil (Tropaquept) were equilibrated with varying concentrations
of KH2PO4. The readily exchangeable portion of the adsorbed P was dete
rmined by anion exchange resin (AER). Considerable hysteresis was obse
rved between adsorbed P and AER-P. To quantify the extent of the hyste
resis, a critical P concentration (P-crit), the amount of P adsorbed a
t zero desorption by AER, was defined. The P-crit of the soils average
d across the soil depths followed the order: Non-Calcic Brown soil > P
lanosol > Alluvial > Cambisol > Lithosol. The P-crit correlated with c
lay and oxalate Fe (Fe-o). The P affinity index (K) estimated by Langm
uir adsorption model accounted for 66% of the variance in P-crit. A se
quential extraction with 0.5 M NaHCO3, 0.1 M NaOH and 11.5 M HCl to re
move the labile, moderately labile and non-labile P forms respectively
, indicated that between 63 and 99% of adsorbed P was in the labile po
ol (AER-P + HCO3-P + OH-P), suggesting that the soils might have high
potential for residual fertilizer-P responses.