The Keumhak Cu deposit is located within the Cretaceous Gyeongsang Basin in the southeastern part of the Korean peninsula. Quartz and calcite vein mineralization in Early Cretaceous sedimentary rocks occurred in three stages: Stage I, quartz+sulfides+ hematite+sulfosalts mineralization; Stage II, quartz+sulfides stage; and Stage III, barren calcite. The main ore mineralization, stage I, can be classified into three substages (pyritic, base-metal, and sulfosalt substages) according to ore mineral assemblages and paragenesis. K-Ar radiometric dating of alteration sericite (77.6±1.6 Ma) indicates that the Cu mineralization of the Keumhak deposit was Late Cretaceous and probably associated with Late Cretaceous granitic rocks that occur near the Keumhak mine.
The Stage I mineralization occurred between >360° and <200°C from fluids with salinities between 5.6 and 1.4 equiv. wt.% NaCl. Most of the Cu mineralization occurred at higher tempera-tures (320° to 280°C). Fluid inclusion data indicate that the main Cu-Pb-Zn ore mineralization resulted from a complex history of CO
2 effervescence coupled with boiling, cooling and dilution of ore fluids. The Cu mineralization was mainly a result of CO
2 effervescence coupled with boiling, whereas the Pb-Zn and the late sulfosalt mineralization resulted mainly from cooling and dilution by an influx of cooler meteoric waters coupled with retrograde boiling. Evidence of fluid unmixing indicates pressures of about 500 bars to 800 bars, and later retrograde boiling evidence indicates that the pressure fluctuated by 200 to 300 bars during hydraulic fracturing.
Sulfur isotope compositions of sulfide minerals in the stage I decrease systematically with paragenetic time with the resultant decrease of calculated δ
34S values of H
2S of 8.4 to 4.7‰. These values, together with the observed change to hematite+sulfides (and/or sulfosalts) assemblages, suggest progressively increasing oxidizing conditions, with a corresponding increase of the sulfate/H
2S ratio of hydrothermal fluids. Gradual increase in the oxidized/reduced sulfur ratio of ore stage fluids led to later mineralization in the stage I through breakdown of metal complexes. Measured and calculated hydrogen and oxygen isotope values of the middle to late ore-forming fluids of the stage I suggest meteoric water dominance, approaching unexchanged meteoric water values, except the
18O-shift.
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