The Hamlin Lake area is located approximately 120km southwest of Thunder Bay, Ontario, in the Shebandowan Greenstone Belt of the Wawa Subprovince in the Superior Province. The area has been explored for its copper and gold mineralization for more than 50 years, but has only recently been treated as an iron-oxide copper gold (IOCG) occurrence. The aim of this study was to characterize the alteration at the occurrence through space and time, and to relate this paragenesis to the formation of mineralization.
Localized field mapping and re-logging of drill core established several relationships between styles of alteration. Rocks were examined in hand specimen and thin section, and minerals were examined with scanning electron microscope (SEM) to identify mineral assemblages and associations. Consistent variations in space could not be mapped, so textural relationships were used to relate the timing between six styles of alteration and the local brecciation that hosts the potential ore. These are: (1) sodic, (2) early potassic, (3) calcic(-iron), (4) late potassic, (5) carbonate, and (6) silicic.
Sodic alteration is largely composed of albitisation, and is occasionally conserved in fragments of the breccia. The early potassic stage of alteration consists of biotite and magnetite in the matrix of the breccia, which is cross-cut by epidote and sphene from the calcic(-iron) stage. Sodium cobaltinitrite staining was used to identify potassium feldspar alteration associated with mineralization of the late potassic stage. The mineralization in this stage is represented by the assemblage chalcopyrite + pyrite + magnetite. This first stage of mineralization was succeeded by carbonate precipitation, and finally by a second stage of mineralization associated with a vuggy quartz breccia.
The two phases of mineralization are primarily different in that stage I mineralization is associated with potassic alteration and iron-oxide mineralization, whereas stage II mineralization is associated with quartz and has a general lack of massive iron-oxide. The alteration leading up to the first stage of mineralization, and the stage I mineralization itself are consistent with the general alteration patterns observed in other magnetite-group IOCG deposits worldwide. The onset of carbonate alteration, followed by vuggy quartz with moderate- to high-sulfidation assemblages of stage II mineralization, is more typical of an epithermal environment.
Thermodynamic parameters of the mineralizing fluids were ascertained by the use of fluid inclusions. Fluid inclusions from the vuggy quartz associated with stage II mineralization were analyzed and suggest a low-salinity fluid with a temperature in the approximate range of 200° to 250°C responsible for mineralization.
Stable oxygen isotopes from chlorite, magnetite and sulphur isotopes from sulphides were measured to establish the source of the fluids responsible for the formation of the deposit. Oxygen from the magnetite of early mineralizing assemblages has a narrow range of values for δ18Owater from +8.9€ to +10.9€. These are indicative of a deep-seated metamorphic or magmatic source for early fluids. Oxygen from chlorite associated with the later stages of mineralization have a wider range of δ18Owater values (+0.4€ to +5.9€), which may suggest that meteoric or other crustally derived fluids played a role in stage II mineralization. δD values were measured on the chlorite as well; however, these may have been reset by later metasomatic events. Sulphur isotope values from mineralization were measured (δ34S -6.9€ to +1.8€), and indicated that an exotic sulphur source probably played a role in mineralization.