Alteration patterns and structural controls of the El Espino IOCG mining district,Chile

The El Espino IOCG mining district is characterized by several mineralized bodies the largest of which is the El Espino deposit, which has an estimated geologic resource of 123 Mt at 0.66 % Cu and 0.24 g/t Au. Mineralized bodies are distributed in a 7?×?10 km² area throughout a 1,000-m vertical section. They range from single veins to stockworks and breccias to manto-type deposits. The ore bodies are hosted primarily by volcanic, volcaniclastic, and sedimentary rocks of the Early Cretaceous Arqueros and Quebrada Marquesa formations, with a few mineralized zones within Late Cretaceous dioritic intrusions. The fault and vein architecture shows that El Espino IOCG system was localized within a dilatational jog along a major transtensional dextral fault system. Sodic alteration (albite) is the most extensive style of alteration in the district, and it is bounded by major NS–NNE trending faults. Sodic–calcic (epidote–albite) alteration occurs at deep to medium elevations (1,000–500 m) and grades inward into calcic alteration. Calcic alteration surrounds dioritic intrusions of the Llahuin plutonic suite. Significant iron oxides are associated with later calcic alteration associations (actinolite–epidote–hematite). The upper portions of the alteration system (0–500 m) display hydrolytic alteration associations with abundant hematite. Hydrolytic veins are feeders to zones of manto-type alteration and mineralization within favorable volcano-sedimentary lithologies that formed El Espino deposit. Sulfides are largely confined to calcic and hydrolytic alteration associations. Hydrothermal fluids responsible for hematite and sulfide mineralization had salinities between 32 and 34 wt% NaCl_eq and temperature of approximately 425 °C at an estimated depth of 3–4 km. Geochronological U–Pb and ⁴⁰Ar/³⁹Ar data indicate that hydrothermal alteration was coeval with magmatic intrusive activity. One particular dioritic intrusion (88.5 Ma) preceded the calcic stage (88.4 Ma), which was accompanied by iron oxide copper and gold mineralization. Hydrolytic alteration, related to economic iron oxide copper and gold mineralization, came immediately after at 87.9 Ma.