“Invisible gold” in pyrite is defined as an Au solid solution of the pyrite lattice, sub-microscopic Au nanoparticles (NPs) in the pyrite, or other chemisorption complexes of Au. Because the relationship between the Au and As concentrations in pyrite could indicate the genesis of the deposit, the purpose of this study is to assess the micro-analytical characteristics of the Au–As relationship in pyrite from epithermal and hydrothermally affected sedimentary Au deposits by secondary ion mass spectrometry. The Au and As concentrations in pyrite vary from 0.04 to 30 ppm and from 1 to 1000 ppm, respectively, in the high-sulfidation Nansatsu-type epithermal deposits; these concentrations are both lower than those of the low-sulfidation epithermal Hishikari deposit. The Au concentrations in pyrrhotite and pyrite reach 6 and 0.3 ppm, respectively, in the Kalahari Goldridge banded-iron-formation-hosted gold deposit, and Au in pyrrhotite may sometimes exist as NPs, whereas As concentrations in pyrrhotite and pyrite are both low and lie in a narrow range from 6 to 22 ppm. Whether Au is present as NPs is important in ore dressing. The Au and As concentrations in pyrite from the Witwatersrand gold field range from 0.02 to 1.1 ppm and from 8 to 4000 ppm, respectively. The shape of the pyrite grains might prove to be an indicator of the hydrothermal influence on deposits of sedimentary origin, which implies the genesis of the deposits.
The Kraaipan and Amalia greenstone belts in South Africa occur in the western part of the Kaapvaal Craton. The two belts stretch discontinuously in an approximately north–south orientation over a distance of about 250 km from southern Botswana in the north to the Vaal River near Christiana in the south and are separated by a distance of about 90 km. Gold mineralization is hosted in banded iron formation at both the Kalahari Goldridge deposit (Kalgold) in the Kraaipan greenstone belt in the north and the Amalia deposit in the Amalia greenstone belt in the south, with the mineralization associated with quartz–carbonate veins. The footwalls of these deposits are generally composed of mafic volcanic schist and the hanging walls consisting of graywackes, schist and shale units. The Kalgold and Amalia gold deposits show some variation in the redox condition of the mineralizing system and fluid chemistry. The ore mineral assemblage is characterized by magnetite–pyrrhotite–pyrite at Kalgold, which is indicative of reducing conditions, and a magnetite–hematite–pyrite assemblage at Amalia that suggests a relatively oxidizing environment. Average mineralizing temperatures determined from chlorite geothermometry were relatively higher at the Kalahari Goldridge deposit ranging from 350 to 400 °C compared to the slightly cooler range of 330 to 390 °C at Amalia. The composition of the fluids derived from fluid inclusions is indicative of low salinity H2O--CO2±CH4-rich fluids at Kalgold against relatively H2O-CO2-rich fluids at Amalia. Evidence from strontium–carbon–oxygen isotopic ratios from carbonates suggests that differences in redox conditions in the deposits could be attributed to different flow pathways by an evolving fluid from a common source (with minimum 87Sr/86Sr = 0.70354) to the sites of gold deposition, with a significant ore fluid interaction with a thick sequence of carbonaceous meta-pelitic rock units at the Kalahari Goldridge deposit that is absent in the Amalia deposit.
The Kraaipan and Amalia greenstone belts in South Africa occurs in the western part of the Kaapvaal Craton. The two belts stretch discontinuously in an approximately north-south orientation over a distance of about 250 km from southern Botswana in the north to the Vaal River near Christiana in the south and are separated by a distance of about 90 km. Gold mineralization is hosted in banded iron-formation at both the Kalahari Goldridge deposit (Kalgold) in the Kraaipan greenstone belt in the north, and the Amalia deposit in the Amalia greenstone belt in the south, with the mineralization associated with quartz-carbonate veins. The footwall of these deposits is generally composed of mafic volcanic schist and hanging wall consisting of graywackes, schist and shale units. The Kalgold and Amalia gold deposits show some variation in the redox condition of the mineralizing system, mineralization temperatures and fluid chemistry. The ore mineral assemblage is characterized by magnetite-pyrrhotite-pyrite at Kalgold, which is indicative of reducing conditions, and magnetite-hematite-pyrite assemblage at Amalia that suggest a relatively oxidizing environment. Average mineralizing temperatures determined from chlorite geothermometry were relatively higher at the Kalahari Goldridge deposit ranging from 350 to 400oC compared to 335 to 370oC (mean, 352± 18, n = 113) at Amalia. The composition of the fluids derived from fluid inclusions are indicative of low salinity H2O-CH4-CO2-rich fluids at Kalgold against relatively H2O-CO2-rich fluids at Amalia. Evidence from strontium-carbon-oxygen isotopic ratios from carbonates suggests differences in redox conditions in the deposits could be attributed to different flow pathways by the evolving fluid from a common source (with minimum 87Sr/86Sr=0.70354) to the sites of gold deposition; with significant ore fluid interaction with thick sequence of carbonaceous meta-pelitic rock units at the Kalahari Goldridge deposit, that is absent in the Amalia deposit.