The Bushveld Igneous Complex (BIC) is known for its laterally extensive platinum group element-bearing layers, the most famous being the Merensky Reef and the UG-2 chromitite in the eastern and western limbs of the complex. In the northern limb, the Platreef mineralization and a thick chromitite seam below it (referred to as the "UG-2 equivalent" or UG-2E) have been proposed to be the stratigraphic equivalents of the Merensky Reef and the UG-2, respectively. In this study, we compare a suite of UG-2E samples from the Turfspruit project with a UG-2 reference suite from the western limb using petrography, electron probe microanalysis, laser ablation-inductively coupled plasma-mass spectrometry, and Mössbauer spectroscopy. The results show that (a) in Mg# vs. Cr# diagrams, UG-2E chromites have a distinct compositional field; however, when samples of similar chromite modal abundance (≥ 80%) are used, the UG-2E chromites overlap the field that characterizes UG-2 chromites; (b) the UG-2E is more variable in chromite modal abundance than the UG-2; and (c) variations in Mg# and Fe/ΣFe in the UG-2E indicate contamination of the magma by metasedimentary rocks of the Duitschland Formation (Transvaal Supergroup) during emplacement, followed by partial re-equilibration of chromite grains with a trapped melt. Thus, we conclude that for chromite modes higher than 80%, the chromite composition retains enough information to allow correlation and that the UG-2E in the northern limb is very likely the UG-2 chromitite.

The abundance and types of reef-bearing carbonate platforms reflect the evolution of Devonian climate, with conspicuous microbial-algal reefs in the warm Early and Late Devonian and sponge-coral reefs in the cooler Middle Devonian. A dolomitized Wenlock-Lower Devonian microbial-algal reef-bearing carbonate platform hosts epigenetic copper-cobalt-germanium (Cu-Co-Ge) sulfide mineralization at Ruby Creek-Bornite in the Brooks Range, Alaska. Here, we present rhenium-osmium (Re-Os) radiometric ages and molybdenum and sulfur (δMo = +2.04 to +5.48‰ and δS = -28.5 to -1.8‰) isotope variations for individual Cu-Co-Fe sulfide phases along the paragenetic sequence carrollite-bornite-pyrite. In the context of a hot, extensional passive margin, greenhouse conditions in the Early Devonian favored restriction of platform-top seawater circulation and episodic reflux of oxidized brines during growth of the carbonaceous carbonate platform. Molybdenum and sulfur isotope data signal the stepwise reduction of hot brines carrying Cu during latent reflux and geothermal circulation for at least ca. 15 million years from the Early Devonian until Cu-Co sulfide mineralization ca. 379-378 million years ago (Ma) in the Frasnian, Late Devonian (weighted mean of Re-Os model ages of carrollite at 379 ± 15 Ma [ = 4]; Re-Os isochron age of bornite at 378 ± 15 Ma [ = 6]). On the basis of petrographic relationships between sulfides and solid bitumen, and the Mo and S isotope data for sulfides, we imply that the endowment in critical metals (e.g., Co, Ge, Re) in the Ruby Creek-Bornite deposit is linked to the activity of primary producers that removed trace metals from the warm Early Devonian seawater and concentrated Co, Ge, and Re in algal-bacterial organic matter in carbonate sediments.

The origin of PGE-Ni-Cu mineralization in the Platreef, northern limb of the Bushveld Igneous Complex (BIC), and the possible correlation with the Merensky Reef in the eastern and western limbs has been long debated. The Platreef and Merensky Reef share the same stratigraphic position in the uppermost part of the Upper Critical Zone (UCZ), near the transition to the overlaying Main Zone (MZ). However, discrepancies in interpretations have been difficult to resolve due to the effects of intense magma-country rock interaction throughout most of the northern limb succession. To address this problem, we generated a detailed stratigraphic profile of the initial strontium isotopic ratio [Sr = (Sr/Sr)] in plagioclase across a Flatreef interval lacking macroscopic evidence of country rock assimilation. The in situ Sr isotopic ratios in plagioclase were determined using LA-MC-ICP-MS analysis on 37 samples from a drill core (UMT094) at the Turfspruit project. Strontium isotope stratigraphy is useful because of a well-documented shift in Sr near the base of the Merensky Unit in the eastern and western limbs. The results show the existence of a significant shift (from Sr = 0.7060 to Sr = 0.7090) that matches the isotopic shift documented through the Merensky Unit in the eastern and western limbs. Thus, this new Sr isotope data indicates that the main mineralized interval of the Flatreef can be stratigraphically correlated to the Merensky Reef in the remainder of the BIC. In addition, we interpret these results as compelling evidence to suggest that the main mineralization processes in the Flatreef were likely similar to those operating in the eastern and western limbs and that interaction with local country rocks was not a necessary condition.

The petrogenesis of extra-large flake graphite is enigmatic. The Bissett Creek graphite deposit, consisting of flake graphite hosted in upper-amphibolite facies quartzofeldspathic gneisses and rare aluminous gneisses, provides an analogue for graphite exploration. In the Bissett Creek gneisses, graphite is homogeneously distributed and composes 2-10 vol. % of the rocks. Disseminated graphite flakes (~ 1 to 6 mm in size) are interleaved with biotite and are petrologically associated with upper-amphibolite facies metamorphic mineral assemblages. Thermobarometry and phase equilibrium modeling yield peak temperatures of > 760 °C at 0.5-0.9 GPa. Whole-rock samples with abundant graphite yield δC from - 28 to - 14‰. δS values of sulfide-bearing samples vary from 10 to 15‰. Sulfur and carbon isotope values are compatible with a biogenic origin, flake graphite probably formed from metamorphism of in situ organic material. However, the variability of δC values from the deposit along with graphite microstructures suggest that carbon-bearing metamorphic fluid (or melt) generated during metamorphism may have remobilized carbon resulting in anomalously large to extra-large flake sizes. This may be a common mechanism globally to explain large graphite flake sizes where graphite formed through in situ metamorphism of organic matter is coarsened due to remobilization of CO-rich fluids (or melt) during high-temperature metamorphism.

The Montecristo district, northern Chile, is one of the few places worldwide where there is a direct relationship between magnetite-(apatite) (MtAp) mineralization and iron oxide-copper-gold (IOCG) mineralization. The MtAp mineralization includes Ti-poor magnetite, fluorapatite, and actinolite and is crosscut and partially replaced by a younger IOCG mineralization that includes a second generation of actinolite and magnetite with quartz, chalcopyrite, pyrite, and molybdenite. The MtAp stage at Montecristo is interpreted as the crystallized iron-rich melts that used the pre-existing structures of the Atacama Fault System as conduits. These rocks later acted as a trap for hydrothermal IOCG mineralization. Geochronology data at Montecristo indicate that the host diorite (U-Pb zircon 153.3 ± 1.8 Ma, 2-sigma), MtAp mineralization (Ar-Ar in actinolite, 154 ± 2 Ma and 153 ± 4 Ma, 2-sigma), and the IOCG event (Re-Os on molybdenite, 151.8 ± 0.6 Ma, 2-sigma) are coeval within error and took place in a time span of less than 3.4 Ma. The εHf and εNd values of the host diorite are + 8.0 to + 9.8 and + 4.3 to + 5.4, respectively. The whole-rock Sr/Sr values of the IOCG mineralization (0.70425 to 0.70442) are in the lower end of those of the MtAp mineralization (0.70426-0.70629). In contrast, εNd values for the IOCG mineralization (+ 5.4 and + 5.7) fall between those of the MtAp rocks (+ 6.6 to + 7.2) and the host diorite, which suggests that the IOCG event was related to fluids having a more crustal Nd (εNd <  + 5.7) composition than the MtAp mineralization. This likely reflects the mixing of Nd from the MtAp protolith and a deep magmatic-hydrothermal source, very likely an unexposed intrusion equivalent to the host diorite. Sulfur isotope compositions (δS, + 0.3 to + 3.4‰) are consistent with a magmatic source.

The Current deposit is hosted by serpentinized peridotite that intruded rocks of the Quetico Subprovince in the Midcontinent Rift, and is subdivided into three morphologically distinct regions - the shallow and thin Current-Bridge Zone in the northwest, the deep and thick 437-Southeast Anomaly (SEA) Zone in the southeast, and the thick Beaver-Cloud Zone in the middle. The magma parental to the Current deposit became saturated in sulfide as a result of the addition of external S from at least two sources - a deep source characterized by high ΔS (< 3‰) values, and a shallow source, potentially the Archean metasedimentary country rocks, characterized by low ΔS (< 0.3‰). Variations in ΔS-S/Se-Cu/Pd values indicate that the contamination signatures were largely destroyed by interaction of the sulfide liquid with large volumes of uncontaminated silicate melt. The intrusion crystallized sequentially, with the Current-Bridge Zone crystallizing first, followed by the Beaver-Cloud Zone, and lastly by the 437-SEA Zone. This, along with the elevated Cu/Pd ratios in the 437-SEA Zone, which formed as a result of sulfide segregation during an earlier saturation event, and development of igneous layering in this zone, suggests that it represents the feeder channel to the Current deposit. After the intrusion crystallized, the base-metal sulfide mineralogy was modified by circulation of late-stage hydrothermal fluids, with pyrrhotite and pentlandite being replaced by pyrite and millerite, respectively. This fluid activity mobilized metals and semi-metals, including Fe, Ni, S, Se, Co, Cu, Ag, and As, but did not affect the PGE. This contribution highlights the importance of the interplay between magma dynamics and magmatic-hydrothermal processes in the formation of Ni-Cu-PGE-mineralized deposits.

The ABM deposit is a bimodal-felsic, replacement-style volcanogenic massive sulfide deposit (VMS) that is hosted by back-arc affinity rocks of the Yukon-Tanana terrane in the Finlayson Lake VMS district, Yukon, Canada. Massive sulfide zones occur as stacked and stratabound lenses subparallel to the volcanic stratigraphy, surrounded by pervasive white mica and/or chlorite alteration. Remnant clasts of volcanic rocks and preserved bedding occur locally within the massive sulfide lenses and indicate that mineralization formed through subseafloor replacement of pre-existing strata. Three mineral assemblages occur at the ABM deposit: (1) a pyrite-chalcopyrite-magnetite-pyrrhotite assemblage that is associated with Cu-Bi-Se-Co-enrichment and occurs at the center of the massive sulfide lenses; (2) a pyrite-sphalerite assemblage, which occurs more commonly towards lens margins and is enriched in Zn-Pb-Ag-Au-Hg-As-Sb-Ba; and (3) a minor assemblage comprising chalcopyrite-pyrrhotite-pyrite stringers associated with pervasive chlorite alteration, which occurs mostly at the sulfide lens margins. Petrographic observations of preserved primary, zone refining, and metamorphic textures in combination with in situ geochemistry show that the pyrite-sphalerite assemblage formed at lower temperatures (< 270 °C) than the other two mineral assemblages (~ 270-350 °C), and that mineral chemistry in all mineral assemblages was affected by greenschist facies metamorphism, although the effects are limited to recrystallization, small-scale remobilization (< 1 m) and trace element redistribution.

The Kirazlı deposit is located at the center of the Biga Peninsula metallogenic province, in a geological setting characterized by an extensional tectonic environment. A NNW-SSE trending high-sulfidation (HS) orebody with a total reserve of 33.86 Mt @ 0.69 g/t Au and 9.42 g/t Ag lies beneath the Kirazlı Main zone. A porphyry Cu orebody hosted by Eocene intrusive and volcanic rocks has been intersected by drilling within its vicinity. The HS epithermal deposit is hosted by a partly silicified and brecciated Oligocene volcanic and volcaniclastic sequence consisting mainly of basaltic andesite lava flow and lithic/crystal tuff. Lithogeochemistry and zircon U-Pb radiometric ages allow us to distinguish three distinct high-K calc-alkaline magmatic events at 41, 38, and 32 Ma, sourced by metasomatized mantle melts, which have interacted with the crust during their ascent. Porphyry Cu mineralization took place at 36.7 ± 0.4 Ma (muscovite Ar/Ar age) with subsequent re-opening and base metal deposition. Crosscutting quartz-pyrite-molybdenite veins were emplaced at 33.6 ± 0.2 Ma (molybdenite Re-Os age), and followed by the HS epithermal Au-Ag event at 31 Ma, based on a previous study. Our radiometric data indicate that the Kirazlı deposit has recorded a long-lasting Cenozoic magmatic and metallogenic evolution during about 10 Myr. Our study demonstrates that successive, independent, and overprinting, but genetically unrelated, HS epithermal precious metal, hydrothermal Mo, base metal, and porphyry Cu systems have been active at the same location during protracted extensional tectonics of the Biga Peninsula.