Abstract

Chemical weathering can be approached from three interpretive points of view: distribution of the secondary minerals in landscapes, weathering of primary minerals and geochemistry of ions in solution. On granitic rocks it is posible to define both climatic and topographic sequences of distribution of clays in association with weathering products: gibbsite - kaolinite - hydrous iron oxides - hydrous manganese oxides - iron-rich montmorillonite - calcium carbonate - calcium sulfate - sodium carbonates and silicates. These stages appear as an absolute accumulation formed by filling of intergranular pores. Another sequence can be found not in intergranular pores but in the cracks and along the cleavages of primary minerals from which they are derived by relative accumulation. The order of appearance of these secondary minerals remains the same regardless of the nature of climates and the topographic position. The conditions of equilibrium are not identical in the interior of grains of different primary minerals nor in the pores outside of them and the secondary minerals found in the different situations are also not identical. This is well demonstrated by the chemistry of waters draining slopes. The equilibrium diagrams and balances between cations and silica sometimes result in disagreement, proving that equilibrium conditions are not satisfied between solutions circulating in the pores and clay minerals found inside the primary minerals.

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