Large variations of aluminium solubilities are found in marine and rur
al precipitations. The results of seven field experiments are used to
produce a model of the solubilization of aluminium independent of the
sampling site. Large variations of solubility appear, and the pH seems
to be a major factor explaining this solubility changes. Thermodynami
c calculations at T = 278K suggest that, at higher pHs (>5), equilibri
um with gibbsite (alphaAl(OH)3) or a trivalent alkaline insoluble form
acts as a limiting of aluminium solubility and at lower pH2 (<5), Al
could be in equilibrium with a hydroxysulfate salt Al(OH)1.5(SO4)0.75.