HYDROTHERMAL FLUID EVOLUTION IN PORPHYRY-TYPE ORE DEPOSITS
Early quartz-rich veins (+-mb) with potassic alteration are comprised of mosaics of CL-bright quartz that lacks euhedral shapes or growth zones. Such quartz is characteristically fractured and cut by later CL-darker quartz with euhedral growth zones. Where Fe and Cu-Fe sulfides are present, they are typically surrounded by late CL-dark quartz. CL-bright quartz typically contains 50-200 ppm Ti and 50-200 ppm Al. Unlike Fe and Cu-Fe sulfides, molybdenite is commonly in direct contact with CL-bright quartz and calcite or anhydrite. In many systems, these veins are dominated by low salinity (3-8 wt %), CO2-bearing (0-10 mol%) B40 fluid inclusions. These inclusions homogenize between 300 and 400°C. Unmixed vapor and brine inclusions are also present in these veins in some systems.
Later pyrite-quartz veins with sericitic alteration typically contain less quartz, which is CL-darker with oscillatory growth zones revealed by CL. This quartz cuts early bright quartz and typically lacks intense fracture networks observed in early veins. Quartz in pyrite-quartz veins typically contains <10 ppm Ti and Al concentrations vary from a ~50-400 ppm. Fluid inclusions in these veins vary, but typically include low salinity, CO2-bearing B60s that homogenize between 350° and 420°C. Unmixed vapor and brines are present, but less common in pyrite-quartz veins in many porphyry deposits.
In many porphyry systems, late sphalerite and galena-bearing veins contain quartz with distinct euhedral growth zones revealed by CL. Quartz in these veins typically contains less than 5 ppm Ti and 10-4000 ppm Al. Fluid inclusions typically contain 10-30% bubble (B20s). These inclusions are low salinity and typically homogenize at temperatures between 180° and 300°C.
Taken together, these data demonstrate the variations in pressure and temperature evolution among various porphyry-type deposits.