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Epithermal deposits occur in many metallogenic belts globally and are economically important sources of precious and base metals. However, post-mineral cover (both transported and younger deposits) also occurs in many prospective districts and hinders exploration efforts. Hydrogeochemistry is a potentially useful exploration tool in these environments, with water–rock interaction shown from other studies to produce large hydrogeochemical footprints. Groundwaters from in and around the Vaquillas (Au-Ag) epithermal deposit in the pre-cordillera of northern Chile are typically Ca-SO 42-  type with meteoric upflow groundwaters interacting with the ore body and producing a significant downflow (down hydraulic head) mobility (up to 3 km) of (oxy)anions of arsenic and molybdenum, which contrasts with proximal trace cation anomalies. Multiple sulphur endmembers contribute to the dissolved sulphate concentrations, including evaporites, primary hypogene sulphide minerals, and a single δ 34 S (SO4)  value of 30.1 ‰ which is potentially associated with disproportionated sulphur in sulphate. This study reports anomalism from one of the most dilute endmember groundwater compositions from Chile reported to date. The sub-alkaline and weakly oxygenated groundwaters are common in many aquifers globally, making the results applicable to many other metallogenic belts. It is also the first hydrogeochemical case study of an intermediate-sulfidation epithermal deposit. Despite the highly dilute groundwaters recharging aquifers at Vaquillas, we conclude hydrogeochemistry to be a highly effective exploration tool for epithermal and porphyry deposits in areas of significant post-mineral cover.

Using groundwater in the hyper-arid Atacama Desert to discover buried hydrothermal mineral deposits