The geochemical evolution of the Catalan potash subbasin, South Pyrenean foreland basin (Spain)

Abstract

Over the last decade, our studies in ancient evaporitic basins have been based on a detailed study of a single borehole record. The detailed findings in medium- to large-sized evaporitic basins were shadowed with a relevant question: can interpretations from a representative evaporitic record in a single borehole be extended to the whole evaporitic basin? This paper addresses that question; the results obtained are compared with results from another distant point within the basin. The general methodology not only proves its reliability in interpreting the evolution of evaporitic basins from a single borehole but reveals its capability to obtain detailed palaeoenvironmental interpretations. The chemical evolution of an Upper Eocene evaporitic sequence from the South Pyrenean foreland basin (Spain) has been investigated along the Súria-19 borehole record. Detailed petrographic and mineralogical study, X-ray microanalysis of frozen primary inclusions trapped in halite (Cryo-SEM-EDS), systematic isotopic analysis ( δ 34S and δ 18O in sulphates) and computer-based evaporation models have been integrated in a multi-proxy methodology. This study revealed that a variable amount of Ca excess is required throughout different parts of the marine Lower Halite Unit (LHU) for sylvite, instead of K–Mg sulphates, to form. This Ca excess is in turn different from that required for the western sector of the same evaporitic basin (Navarrese subbasin). Quick and variable changes in Ca-rich brines or equivalent dolomitization required are explained as internal processes within the basin rather than secular variations in seawater chemistry. The general hydrological evolution of the Catalan subbasin is explained as a restricted subbasin with a first marine stage in which continental input (up to 50% of total input) had an important control on the geochemistry of the subbasin. A second stage was determined during potash precipitation, in which the subbasin was cut from any seawater input to end up in its last stage as a purely continental evaporitic basin. Coupling evaporation models and analytical results we have obtained the proportions of recycling and their sources, estimated to change from a 100% (total mass of sulphate) Eocene source to 20% Eocene and 80% Triassic (Keuper) towards the latest stage of potash precipitation. The results obtained have been compared with results from the Navarrese subbasin allowing an integrated interpretation of the hydrological evolution of the whole Upper Eocene South Pyrenean basin. Local geochemical variations within the Upper Eocene south Pyrenean basin are explained by the differences in paleogeographical setting of the Navarrese and Catalan subbasins.