The adsorption-desorption of cadmium (Cd) as a function of pH, ionic s
trength, and composition of the electrolyte was examined for four vari
able charge soils: two Alfisols from Zimbabwe (Mazowe and Bulawayo) an
d two Andisols from Spain (Realejos-1 and Realejos-2), At the natural
soil pH, Cd adsorption measured in 0.01 mol dm(-3) NaNO3 was related t
o the net negative surface charge of the soils, Most of the Cd adsorbe
d in the four soils was strongly bonded, Increasing pH increased the s
urface negative charge of all soils, Adsorption of Cd also increased c
ontinuously with rising pH, and part of the variation in adsorption wi
th pH was explained by the variation in the negative surface charge, D
esorption decreased as the pH increased and became a trace at pH > 6.
Differences in extractability between the two groups of soils were con
sidered to be related to differences in the characteristics of the soi
l matrix, Increasing the concentration of the electrolyte from 0.001 t
o 0.1 mol dm(-3) NaNO3 caused a decrease in Cd adsorption and enhanced
the amount of sorbed metal that could subsequently be desorbed, Varia
tions in the initial pH of the soil suspensions, however, accounted fo
r part of the effect, This pH-ionic strength interaction was even more
evident when the most dilute electrolyte was used, Adsorption was red
uced in the Ca-electrolyte compared with the Na-electrolyte, Calcium,
on the contrary. increased Cd desorption.