The impact of kaolinite and oxi-hydroxides on nitrate adsorption in deep layers of a Costarican Acrisol under coffee cultivation

A nitrogen budget study of a highly fertilized coffee plantation growing on an Acrisol (Ultisol: Ustic Paleohumult) in Southern Costa Rica provided clear evidence of low nitrate (NO3−) leaching to groundwater, in spite of a large annual rainfall and fairly high soil permeability. In this study, conducted at the same site, we measured soil properties in relation to nitrate adsorption. The clay content and proportion of kaolinite were high in the 80–200cm layer and decreased below, whereas the proportion of gibbsite and to a lesser extent of iron oxi-hydroxides increased below 200cm. Nitrate adsorption isotherms were measured. Nitrate adsorption maxima [coefficient a (Nmax) of the Langmuir equation] ranged from 1.9 to 1.6cmolc kg−1 between 80 and 200cm depth and decreased below to reach a value of 0.9cmolc kg−1 at 380cm depth. Anion exchange capacity and nitrate adsorption maxima were positively correlated with the clay and kaolinite contents, and negatively with gibbsite content and the net charge, assessed from the difference between soil pH in KCl and in distilled water. Nevertheless, the sorption affinity of NO3− to mineral surfaces, (coefficient b of the Langmuir equation), was highly correlated with the net charge and with the occurrence of gibbsite and iron oxi-hydroxides. We measured in the field a large NO3−–N accumulation in the sub-soil (up to 1570kg of NO3−–Nha−1 retained between 80 and 380cm depth). In the layer 80–200cm, where the clay size fraction was dominated by kaolinite, 55 to 75% of the stored NO3− could be extracted by shaking soil in distilled water. In this soil layer, the NO3− content was positively related to the net positive charge. In the layer 200–380cm, where the clay size fraction was dominated by gibbsite, the proportion of NO3− extractable in distilled water was lower (45%) than above.