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Geoderma 106 (2001) 83-100
Distribution and Dynamic of Gibbsite and Kaolinite in an Oxisol of Serra do Mar, southeastern Brazil
S. Furian 1, Laurent Barbiero 2, René Boulet 3, 4, Pierre Curmi 5, Michel Grimaldi 6, 7, Catherine Grimaldi 8
(13/06/2001)

In the Serra do Mar region, in southeastern Brazil, the soil mantle is mainly characterised by (i) a gibbsitic saprolite, (ii) various kaolinitic horizons within the gibbsitic material, (iii) kaolinito-gibbsitic topsoil horizons. This organisation does not match with the thermodynamic stability of gibbsite and kaolinite accompanying the solution percolation through soil profiles. A study of the micromorphological, mineralogical and chemical properties of the soil mantle reveals that this organisation arises from the in situ development of the soil from the crystalline bedrock. The bauxitic weathering of the bedrock, even if it is rich in quartz, can be explained by a fast renewal of the solutions and/or a high solubility of the kaolinite. Recycling of Si and Al by the forest can maintain a dynamic equilibrium of Kaolinite in the topsoil horizons, as observed in Amazonia. The kaolinitic compact horizons evolve upslope at the expend of the gibbsitic material. At the contact between kaolinitic and gibbsitic material, dissolution patterns of quartz and gibbsite are observed, indicating that this evolution is in process. These observations and the organisation of the soil mantle set the problem of the apparent stability of gibbsite and kaolinite in this environment. Various assumptions that could explain this organisation of the soil mantle are discussed. Changes in the activity of water due to the pore size diminution, and displacement of the gibbsite-kaolinite equilibrium appear insufficient to explain the stability of kaolinite. However, it could be alloted to the slow down of water flows in the soil mantel. Lastly, the eventual role of the complexing organic matter is presented. More investigations on the biogeochemical cycle of Si and Al and on the physico-chemical processes at the soil solution-mineral interface are necessary to explain the stability and dynamic of gibbsite and kaolinite in this environment.
1 :  Laboratório de Pedologia, Departamento de Geografia
Universidade Federal do Mato Grosso do Sul
2 :  Laboratoire des Mécanismes et Transfert en Géologie (LMTG)
CNRS : UMR5563 – Observatoire Midi-Pyrénées – Université Paul Sabatier [UPS] - Toulouse III – Institut de recherche pour le développement [IRD] : UMR154
3 :  Universidade de São Paulo
Universidade de São Paulo
4 :  ORSTOM-NUPEGEL
Universidade de São Paulo
5 :  ENESAD
Ecole Nationale Supérieure d'Agronomie de Dijon
6 :  Unité mixte de physique CNRS/Thalès (UMP CNRS/THALES)
CNRS : UMR137 – THALES
7 :  Biodiversité et fonctionnement du sol (BIOSOL)
Institut de recherche pour le développement [IRD] – Université Pierre et Marie Curie [UPMC] - Paris VI – Université Paris VII - Paris Diderot – Université Paris-Est Créteil Val-de-Marne (UPEC)
8 :  Sol Agro et hydrosystème Spatialisation (SAS)
Institut national de la recherche agronomique (INRA) : UR1069 – Ecole Nationale Supérieure Agronomique de Rennes
Planète et Univers/Sciences de la Terre
Gibbsite – Kaolinite – Resilication – Mineral stability – Brazil
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