Hydrothermal Mineralization and Mineral Chemistry of Arsenides and Sulfarsenides in the Fe-Co-Ni-As-S System and Introduction of Three Unique Minerals, Port Radium Deposit, Canada.

The Port Radium U-Cu-Ni-Co-Ag deposit in northwestern Canada is hosted within a mineral system that has generated a variety of mineralization styles from iron oxide-copper-gold to iron oxide-apatite, porphyry, skarn, and epithermal. Their genesis is linked to an extensive subduction-related magmatism that formed widespread dacite-rhyodacite-andesite volcanic and volcanoclastic sequences (~1.87 Ga), which have been intruded by their equivalent intrusive plutons. Pervasive and intensive hydrothermal alterations, including albitic, magnetite-actinolite-apatite, potassic ± albitic, phyllic, and propylitic occurred before the main sulfide, sulfarsenide, and uraninite vein-type mineralization. Although scarce sulfide minerals formed at the beginning of the hydrothermal activity, the main polymetallic arsenide-sulfarsenide-sulfide ± uraninite vein-type mineralization occurred during the epithermal stage. In addition to the common arsenides and sulfarsenides including nickeline, cobaltite, rammelsbergite, safflorite, skutterudite, gersdorffite, and arsenopyrite, three unique sulfarsenides were also found: Co_0.67Ni_0.32Fe_0.02S_0.19As_2.80, which could be a sulfur-rich skutterudite, Ni_0.85Co_0.15S_0.39As_1.60, and Ni_0.69Co_0.31S_0.47As_1.52, which are chemically comparable to the Port Radium rammelsbergite with substantial addition of S and Co; they could be the solid solution product of gersdorffite-cobaltite or safflorite-rammelsbergite. [ABSTRACT FROM AUTHOR]