Mineralogical and chemical zonations observed in massive sulfide ores from Ni-Cu-platinum group element (PGE) deposits are commonly ascribed to the fractional crystallization of monosulfide solid solution (MSS) and intermediate solid solution (ISS) from sulfide liquid. Recent studies of classic examples of zoned orebodies at Sudbury and Voisey’s Bay (Canada) demonstrated that the chemistry of magnetite crystallized from sulfide liquid was varying in response to sulfide fractional crystallization. Other classic examples of zoned Ni-Cu-PGE sulfide deposits occur in the Norilsk-Talnakh mining district (Russia), yet magnetite in these orebodies has received little attention. In this contribution, we document the chemistry of magnetite in samples from Norilsk-Talnakh, spanning the classic range of sulfide composition, from Cu poor (MSS) to Cu rich (ISS). Based on textural features and mineral associations, four types of magnetite with distinct chemical composition are identified: (1) MSS magnetite, (2) ISS magnetite, (3) reactional magnetite (at the sulfide-silicate interface), and (4) hydrothermal magnetite (resulting from sulfide-fluid interaction). Compositional variability in lithophile and chalcophile elements records sulfide fractional crystallization across MSS and ISS magnetites and sulfide interaction with silicate minerals (reactional magnetite) and fluids (hydrothermal magnetite). Estimated partition coefficients for magnetite in sulfide systems are unlike those in silicate systems. In sulfide systems, all lithophile elements are compatible and chalcophile elements tend to be incompatible with magnetite, but in silicate systems some lithophile elements are incompatible and chalcophile elements are compatible with magnetite. Finally, comparison with magnetite data from other Ni-Cu-PGE sulfide deposits pinpoints that the nature of parental silicate magma, degree of sulfide evolution, cocrystallizing phases, and alteration conditions influence magnetite composition.

The titanomagnetite of the Lac Doré Complex, an Archean layered intrusion that is located in the Abitibi greenstone belt in Québec (Canada), contains a wide variety of exsolution textures, which are the remnants of a complex cooling history. In the present study, we reconstitute the decomposition stages of the original solid solution in order to explain the formation of ilmenite, Al-spinel (hercynite and gahnite), and corundum exsolutions in magnetite. This was conducted through a detailed mineralogical and textural examination and in situ determination of mineral chemistry. Our investigation reveals two discrete types of ilmenite exsolutions, which are ascribed, respectively, to the oxidation of ulvöspinel at temperatures above and below the magnetite-ulvöspinel solvus. Exsolutions of Al-spinel result from either a decrease in the solubility of the (FeZn)Al₂O₄ components upon cooling, or local excesses of Al and Zn due to the removal of ulvöspinel during the early oxidation. The origin of corundum is ascribed to the oxidation of pre-existing hercynite exsolutions. The trace element composition of the titanomagnetite indicates stratigraphic reversals in Cr, Mg, Co, Ti, and Si and important changes in redox conditions. We interpret this as a direct consequence of a major event of magma chamber replenishment, which strongly influenced the distribution of exsolutions.