DIVERSITY OF INTENSE ACID (ADVANCED ARGILLIC) ALTERATION
AAA is typically silica-saturated and ranges from low-T (25-250ºC) kaolinite-stable to high-T (400-600ºC) andalusite-stable assemblages; these features and accessory phases vary with setting. AAA varies markedly in oxidation state, sulfidation state and sulfide contents ranging from (1) high-sulfidation, S-rich (5-20% pyrite) in porphyry and epithermal systems, to (2) lower sulfidation S-poor (0-2% pyrite, common hypogene Fe oxides) in several settings including IOCG systems, to (3) to sulfate-bearing (typ. alunite) sulfide-poor, oxidized assemblages in near surface systems. Bulk metal contents and ratios vary widely (e.g., Ag:Au in high sulfidation AAA varies from <1 to >100; high to absent As, Hg); in some cases metals are leached or absent (e.g., IOCGs, some pyrophyllite deposits).These characteristics require different fluids and processes – including but not limited to the familiar SO2-driven (porphyry, epithermal), steam-heated (geothermal), and weathering-related mechanisms.
As is well established, SO2-rich hydrothermal fluids of magmatic derivation are most common; yet even they exhibit large differences in element enrichments requiring that other factors be important including differences in magmatic compositions and vapor vs. brine transport. Low sulfur systems require other acid sources, in IOCG and perhaps other settings this is likely HCl and metal chlorides, factors that in turn will govern distinctive element enrichments. Supported by NSF EAR08-38157 and USGS MRERP 08HQGR0060.