Abstract

Summary Groundwater from the fractured basalt Serra Geral Aquifer (SGA) represents an important source for water supply in Northeastern Sao Paulo state (Brazil). Groundwater flow conditions in fractured aquifers hosted in basaltic rocks are difficult to define because flow occurs through rock discontinuities. The evaluation of hydrodynamic information associated with hydrochemical data has identified geochemical processes related to groundwater evolution, observed in regional flowpaths. SGA groundwaters are characterized by low TDS with pH varying from neutral to alkaline. Two main hydrochemical facies are recognized: Ca–Mg–HCO 3 , and Na–HCO 3 types. Primarily, the geochemical evolution of SGA groundwater occurs under CO 2 open conditions, and the continuous uptake of CO 2 is responsible for mineral dissolution, producing bicarbonate as the main anion, and calcium and magnesium in groundwater. Ion exchange between smectites (Na and Ca-beidelites) seems to be responsible for the occurrence of Na–HCO 3 groundwater. Toward the Rio Grande, in the northern portion of the study area, there is mixing between SGA groundwater and water from the sandstones of the Guarani Aquifer System, as evidenced by the chemical and isotopic composition of the groundwater. Inverse mass balance modeling performed using NETPATH XL produces results in agreement with the dissolution of minerals in basalt (feldspars and pyroxenes) associated with the uptake of atmospheric CO 2 , as well as the dissolution of clay minerals present in the soil. Kaolinite precipitation occurs due to the incongruent dissolution of feldspars, while Si remains almost constant due to the precipitation of silica. The continuous uptake of CO 2 under open conditions leads to calcite precipitation, which in addition to ion exchange are responsible by Ca removal from groundwater and an increase in Na concentrations. Down the flow gradientCO 2 is subject to closed conditions where the basalts are covered by the sediments of Bauru Group or associated with deeper isolated discontinuities. A decrease in the amount of dissolution of labradorite and augite is observed, associated with precipitation of carbonates and kaolinite. Stable isotope ratios of SGA groundwater vary from −37.8‰ to −61.3‰ VSMOW for δ 2 H VSMOW, and −5.7‰ to −8.9‰ VSMOW for δ 18 O, indicating temporal variations in climatic conditions during recharge.

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