PGE geochemistry of the Eagle Ni–Cu–(PGE) deposit, Upper Michigan: constraints on ore genesis in a dynamic magma conduit

The Eagle Ni–Cu–(PGE) deposit is hosted in mafic–ultramafic intrusive rocks associated with the Marquette–Baraga dike swarm in northern Michigan. Sulfide mineralization formed in association with picritic magmatism in a dynamic magma conduit during the early stages in the development of the ~1.1?Ga Midcontinent Rift System. Four main types of sulfide mineralization have been recognized within the Eagle deposit: (1) disseminated sulfides in olivine-rich rocks; (2) rocks with semi-massive sulfides located both above and below the massive sulfide zone; (3) massive sulfides; and (4) sulfide veins in sedimentary country rocks. The disseminated, massive and lower semi-massive sulfide zones are typically composed of pyrrhotite, pentlandite and chalcopyrite, whereas the upper semi-massive sulfide ore zone also contains pyrrhotite, pentlandite, and chalcopyrite, but has higher cubanite content. Three distinct types of sulfide mineralization are present in the massive sulfide zone: IPGE-rich, PPGE-rich, and PGE-unfractioned. The lower and upper semi-massive sulfide zones have different PGE compositions. Samples from the lower semi-massive sulfide zone are characterized by unfractionated PGE patterns, whereas those from the upper semi-massive sulfide zone show moderate depletion in IPGE and moderate enrichment in PPGE. The mantle-normalized PGE patterns of unfractionated massive and lower semi-massive sulfides are subparallel to those of the disseminated sulfides. The results of numerical modeling using PGE concentrations recalculated to 100% sulfide (i.e., PGE tenors) and partition coefficients of PGE between sulfide liquid and magma indicate that the disseminated and unfractionated massive sulfide mineralization formed by the accumulation of primary sulfide liquids with similar R factors between 200 and 300. In contrast, the modeled R factor for the lower semi-massive sulfide zone is <100. The fractionated sulfide zones such as those of the IPGE-rich and PPGE-rich massive sulfides and the upper semi-massive sulfide zone can be explained by fractional crystallization of monosulfide solid solution from sulfide liquids. The results of numerical modeling indicate that the sulfide minerals in the upper semi-massive sulfide zone are the products of crystallization of fractionated sulfide liquids derived from a primary sulfide liquid with an R factor similar to that for the disseminated sulfide mineralization. Interestingly, the modeled parental sulfide liquid for the IPGE-rich and PPGE-rich massive sulfide zones has a higher R factor (~400) than that for the unfractionated massive sulfide mineralization. Except one sample which has unusually high IPGE and PPGE contents, all other samples from the Cu-rich sulfide veins in the footwall of the intrusion are highly depleted in IPGE and enriched in PPGE. These signatures are generally consistent with highly fractionated sulfide liquids expelled from crystallizing sulfide liquid. Collectively, our data suggest that at least four primary sulfide liquids with different R factors (<100, 200–300, ~400) were involved in the formation of the Eagle magmatic sulfide deposit. We envision that the immiscible sulfide liquids were transported from depth by multiple pulses of magma passing through the Eagle conduit system. The sulfide liquids were deposited in the widened part of the conduit system due to the decreasing velocity of magma flow. The presence of abundant olivine in some of the sulfide ore zones indicates that the ascending magma also carried olivine crystals. Sulfide saturation was attained in the parental magma due in large part to the assimilation of country rock sulfur at depth.     

Ni–Cu–(PGE) magmatic sulfide deposits in the Yangliuping area,Permian Emeishan igneous province,SW China

The Ni–Cu–PGE sulfide deposits in the Yangliuping area, SW China, are hosted in mafic–ultramafic sills. The four mineralized sills are located in the Yangliuping tectonic dome and intrude Devonian carbonaceous marble, graphitic schist. The sills are 200–300 m thick and 1,000–2,000 m in strike length and now consist chiefly of serpentinite, talc schist, tremolite schist, and meta-gabbro. Disseminated Ni–Cu sulfide mineralisation occurs in the serpentinite in the lower parts of the sills. Massive sulfide mineralisation is located in the base of the sills and in the footwall along fractures beneath the mineralized serpentinite. Although the sulfide ores have been modified by hydrothermal activity, there are relict cumulate textures in the disseminated sulfides indicating a magmatic origin for the ores. The Yangliuping Intrusions and the Dashibao Formation have similar primitive-mantle normalized trace element and platinum group element (PGE) patterns, indicating that they are derived from a common parental magma type. The positive correlation between Cu concentrations and Cu/Zr ratios of the Dashibao Formation basalts indicates that the chalcophile elements were removed before eruption. We propose that fractional crystallization of the Yangliuping magma accompanied by the introduction of S and CO₂ from the wall rocks caused the magma to become S-saturated leading to the segregation of magmatic sulfides that became enriched in Ni–Cu–(PGE). The sills acted as conduits for the overlying Dashibao Formation basalts with the sulfide liquid, along with early crystallizing olivine and pyroxene, segregating from the magma as it passed through the conduits prior to eruption.Editorial handling: H.E. Frimmel     

The composition of magmatic Ni–Cu–(PGE) sulfide deposits in the Tati and Selebi-Phikwe belts of eastern Botswana

We studied a number of magmatic Ni–Cu–(PGE) sulfide deposits in two distinct belts in eastern Botswana. The Tati belt contains several relatively small deposits (up to 4.5 Mt of ore at 2.05% Ni and 0.85% Cu) at Phoenix, Selkirk and Tekwane. The deposits are hosted by ca 2.7 Ga, low- to medium-grade metamorphosed gabbroic–troctolitic intrusions situated within or at the periphery of a greenstone belt. The deposits of the Selebi-Phikwe belt are larger in size (up to 31 Mt of ore grade). They are hosted by high-grade metamorphosed gabbronorites, pyroxenites and peridotites believed to be older than ca 2.0 Ga that intruded gneisses of the Central Zone of the Limpopo metamorphic belt. The composition of the sulfide mineralisation in the two belts shows systematic variation. Most of the mineralisation in the Tati belt contains 2–9% Ni and 0.05–4% Cu (Cu/Cu + Ni = 0.4–0.7), whereas most of the mineralisation in the Selebi-Phikwe belt contains 1–3% Ni and 0.1–4% Cu (Cu/Cu + Ni = 0.4–0.9). The Cu–Ni tenors of the ores in both belts are consistent with crystallization from a basaltic magma. The Tati ores contain mostly >3 ppm Pt + Pd (Pt/Pd 0.1–1), with Pd/Ir = 100–1,000, indicative of a differentiated basaltic magma that remained S-undersaturated before emplacement. Most of the Selebi-Phikwe ores have <0.5 ppm Pt + Pd (Pt/Pd < 0.1–1), with Pd/Ir = 10–500. This suggests a relatively less differentiated magma that reached S saturation before emplacement. The Tati rocks show flat mantle-normalised incompatible trace element patterns (average Th/Yb_N = 1.57), except for strong enrichments in large ion lithophile elements (Cs, Rb, Ba, U, K). Such patterns are characteristic of relatively uncontaminated oceanic arc magmas and suggest that the Tati intrusions were emplaced in a destructive plate margin setting. Most of the Selebi-Phikwe rocks (notably Dikoloti) have more fractionated trace element signatures (average Th/Yb_N = 4.22), possibly indicating digestion of upper crustal material during magma emplacement. However, as there are also samples that have oceanic arc-like signatures, an alternative possibility is that the composition of most Selebi-Phikwe rocks reflects tectonic mingling of the intrusive rocks with the country rocks. The implication is that orogenic belts may have a higher prospectivity for magmatic Ni–Cu ores than presently recognised. The trigger mechanism for sulfide saturation and segregation in all intrusions remains unclear. Whereas the host rocks to the intrusions appear to be relatively sulfur poor, addition of crustal S to the magmas is suggested by low Se/S ratios in some of the ores (notably at Selebi-Phikwe). External S sources may thus remain unidentified due to poor exposure and/or S mobility in response to metamorphism.     

Metamorphic degassing of carbonates in the contact aureole of the Aguablanca Cu–Ni–PGE deposit,Spain

Analysis of magmatic and sedimentary rocks of several large igneous provinces has demonstrated that the release of gas during plutonic-metamorphic processes may be linked to global climate change and mass extinctions. Aguablanca, one of the largest Cu–Ni–PGE deposits in Europe, formed during the Variscan orogeny when a mafic magma intruded limestones and shales, creating a contact aureole composed of marble, skarn and hornfels. Our petrological and geochemical investigation of the aureole provides evidence that a combination of the two processes led to the formation of the ore deposit: The assimilation of terrigenous sediments supplied S to the magma while the assimilation of carbonates changed the oxygen fugacity and decreased the solubility of sulfur in the magma. The metamorphic assemblages in the contact aureole are directly related to heterogeneity of the protolith and particularly to the original proportions of calcite and clay. We modeled carbon dioxide degassing during contact metamorphism and showed that pure limestone is relatively unproductive because of its high reaction temperature. The presence of clay, however, leads to the formation of calc-silicates and significantly enhances CO₂ degassing. Our estimations suggest that degassing of the Aguablanca contact aureole released about 74.8 Mt of CO₂, a relatively low volume that we attribute to the composition of the host rock, mainly a pure limestone. A far larger volume of carbon dioxide was emitted by the contact metamorphism of dolostones in the contact aureole of Panzhihua (part of Emeishan large igneous province, SW China). We propose that the level of emission of carbon dioxide depends strongly on the nature of the protolith and has to be considered when predicting environmental impact during the emplacement of large igneous provinces.     

Geochemistry of the Kalatongke Ni–Cu–(PGE) sulfide deposit,NW China: implications for the formation of magmatic sulfide mineralization in a postcollisional environment

The Kalatongke (also spelt as Karatungk) Ni–Cu–(platinum-group element, PGE) sulfide deposit, containing 33 Mt sulfide ore with a grade of 0.8 wt.% Ni and 1.3 wt.% Cu, is located in the Eastern Junggar terrane, Northern Xinjiang, NW China. The largest sulfide ore body, which occupies more than 50 vol.% of the intrusion Y1, is dominantly comprised of disseminated sulfide with a massive sulfide inner zone. Economic disseminated sulfides also occur at the base of the intrusions Y2 and Y3. The main host rock types are norite in the lower part and diorite in the upper part of each intrusion. Enrichment in large ion lithophile elements and depletion in heavy rare earth elements relative to mid-ocean ridge basalt indicate that the mafic intrusions were produced from magmas derived from a metasomatized garnet lherzolite mantle. The average grades of the disseminated ores are 0.6 wt.% Ni and 1.1 wt.% Cu, whereas those of the massive ores are 2 wt.% Ni and 8 wt.% Cu. The PGE contents of the disseminated ores (14–69 ppb Pt and 78–162 ppb Pd) are lower than those of the massive ores (120–505 ppb Pt and 30–827 ppb Pd). However, on the basis of 100% sulfide, PGE contents of the massive sulfides are lower than those of the disseminated sulfides. Very high Cu/Pd ratios (>4.5 × 10⁴) indicate that the Kalatongke sulfides segregated from PGE-depleted magma produced by prior sulfide saturation and separation. A negative correlation between the Cu/Pd ratio and the Pd content in 100% sulfide indicates that the PGE content of the sulfide is controlled by both the PGE concentrations in the parental silicate magma and the ratio of the amount of silicate to sulfide magma. The negative correlations between Ir and Pd indicate that the massive sulfides experienced fractionation.     

The distribution of platinum group elements (PGE) and other chalcophile elements among sulfides from the Creighton Ni–Cu–PGE sulfide deposit, Sudbury, Canada, and the origin of palladium in pentlandite

Concentrations of platinum group elements (PGE), Ag, As, Au, Bi, Cd, Co, Mo, Pb, Re, Sb, Se, Sn, Te, and Zn, have been determined in base metal sulfide (BMS) minerals from the western branch (402 Trough orebodies) of the Creighton Ni–Cu–PGE sulfide deposit, Sudbury, Canada. The sulfide assemblage is dominated by pyrrhotite, with minor pentlandite, chalcopyrite, and pyrite, and they represent monosulfide solid solution (MSS) cumulates. The aim of this study was to establish the distribution of the PGE among the BMS and platinum group minerals (PGM) in order to understand better the petrogenesis of the deposit. Mass balance calculations show that the BMS host all of the Co and Se, a significant proportion (40–90%) of Os, Pd, Ru, Cd, Sn, and Zn, but very little (<35%) of the Ag, Au, Bi, Ir, Mo, Pb, Pt, Rh, Re, Sb, and Te. Osmium and Ru are concentrated in equal proportions in pyrrhotite, pentlandite, and pyrite. Cobalt and Pd (∼1 ppm) are concentrated in pentlandite. Silver, Cd, Sn, Zn, and in rare cases Au and Te, are concentrated in chalcopyrite. Selenium is present in equal proportions in all three BMS. Iridium, Rh, and Pt are present in euhedrally zoned PGE sulfarsenides, which comprise irarsite (IrAsS), hollingworthite (RhAsS), PGE-Ni-rich cobaltite (CoAsS), and subordinate sperrylite (PtAs₂), all of which are hosted predominantly in pyrrhotite and pentlandite. Silver, Au, Bi, Mo, Pb, Re, Sb, and Te are found predominantly in discrete accessory minerals such as electrum (Au–Ag alloy), hessite (Ag₂Te), michenerite (PdBiTe), and rhenium sulfides. The enrichment of Os, Ru, Ni, and Co in pyrrhotite, pentlandite, and pyrite and Ag, Au, Cd, Sn, Te, and Zn in chalcopyrite can be explained by fractional crystallization of MSS from a sulfide liquid followed by exsolution of the sulfides. The early crystallization of the PGE sulfarsenides from the sulfide melt depleted the MSS in Ir and Rh. The bulk of Pd in pentlandite cannot be explained by sulfide fractionation alone because Pd should have partitioned into the residual Cu-rich liquid and be in chalcopyrite or in PGM around chalcopyrite. The variation of Pd among different pentlandite textures provides evidence that Pd diffuses into pentlandite during its exsolution from MSS. The source of Pd was from the small quantity of Pd that partitioned originally into the MSS and a larger quantity of Pd in the nearby Cu-rich portion (intermediate solid solution and/or Pd-bearing PGM). The source of Pd became depleted during the diffusion process, thus later-forming pentlandite (rims of coarse-granular, veinlets, and exsolution flames) contains less Pd than early-forming pentlandite (cores of coarse-granular).     

Anorthosites of the Low-sulfide Platiniferous Horizon (Reef I) in the Upper Riphean Yoko–Dovyren Massif (Northern Cisbaikalia): New Data on the Composition,PGE–Cu–Ni Mineralization,Fluid Regime,and Formation Conditions

Geology of Ore Deposits - Recent investigations have made it possible to update the mineralogical, petrochemical, and geochemical characteristics of anorthosites, which are considered the main link...     

Change in carbon flux (1960–2015) of the Red River (Vietnam)

Global riverine carbon concentrations and fluxes have been impacted by climate and human-induced changes for many decades. This paper aims to reconstruct the longterm carbon concentrations and carbon fluxes of the Red River, a system under the coupled pressures of environmental change and human activity. Based on (1) the relationships between particulate and dissolved organic carbon (POC, DOC) or dissolved inorganic carbon (DIC), and suspended sediments (TSS) or river water discharge and on (2) the available detailed historical records of river discharge and TSS concentration, the variations of the Red River carbon concentration and flux were estimated for the period 1960–2015. The results show that total carbon flux of the Red River averaged 2555?±?639 kton C year^?1. DIC fluxes dominated total carbon fluxes, representing 64% of total, reflecting a strong weathering process from carbonate rocks in the upstream basin. Total carbon fluxes significantly decreased from 2816 kton C year^?1 during the 1960s to 1372 kton C year^?1 during the 2010s and showed clear seasonal and spatial variations. Organic carbon flux decreased in both quantity and proportion of the total carbon flux from 40.9% in 1960s to 14.9% in 2010s, reflecting the important impact of dam impoundment. DIC flux was also reduced over this period potentially as a consequence of carbonate precipitation in the irrigated, agricultural land and the reduction of the Red River water discharge toward the sea. These decreases in TSS and carbon fluxes are probably partially responsible for different negatives impacts observed in the coastal zone.     

Metal sources for the polymetallic Ni–Mo–PGE mineralization in the black shales of the Lower Cambrian Niutitang Formation,South China

Total organic carbon content (TOC), trace element and platinum-group element (PGE) concentrations were determined in the black shales of the Lower Cambrian Niutitang Formation in the Nayong area, Guizhou Province, South China, in order to study the polymetallic Ni–Mo–PGE mineralization. The results demonstrate that numerous elements are enriched in the polymetallic ores compared to those of the nearby black shale, particularly Ni, Mo, Zn, TOC and total PGE, which can reach up to 7.03 wt.%, 8.49 wt.%, 11.7 wt.%, 11.5 wt.% and 943 ppb, respectively. The elemental enrichment distribution patterns are similar to those in the Zunyi and Zhangjiajie areas except that the Nayong location is exceptionally enriched in Zn. Whereas positive correlations are observed between the ore elements of the polymetallic ores, no such correlations are observed in the black shale. These positively correlated metallic elements are classified into three groups: Co–Ni–Cu–PGE, Zn–Cd–Pb and Mo–Tl–TOC. The geological and geochemical features of these elements suggest that Proterozoic and Early Palaeozoic mafic and ultramafic rocks, dolomites and/or Pb–Zn deposits of the Neoproterozoic Dengying Formation and seawater could be the principal sources for Co–Ni–Cu–PGE, Zn–Cd–Pb, and Mo–Tl–TOC, respectively. Furthermore, the chondrite-normalized patterns of PGEs with Pd/Pt, Pd/Ir and Pt/Ir indicate that PGE enrichment of the polymetallic ores is most likely related to hydrothermal processes associated with the mafic rocks. In contrast, PGE enrichment in the black shale resembles that of the marine oil shale with terrigenous and seawater contributions. Our investigations of TOC, trace elements and PGE geochemistry suggest that multiple sources along with submarine hydrothermal and biological contributions might be responsible for the formation of the polymetallic Ni–Mo–PGE mineralization in the black shales of the Lower Cambrian Niutitang Formation across southern China.     

Oceanic lithosphere heterogeneity in the eastern Paleo-Tethys revealed by PGE and Re–Os isotopes of mantle peridotites in the Jinshajiang ophiolite

Platinum group elements (PGE) and Re–Os isotopes of mantle peridotites in the Jinshajiang ophiolite (SW China) were investigated in this study, in order to cons...     

The long-term trends (1982–2006) in vegetation greenness of the alpine ecosystem in the Qinghai-Tibetan Plateau

The increased rate of annual temperature in the Qinghai-Tibetan Plateau exceeded all other areas of the same latitude in recent decades. The influence of the warming climate on the alpine ecosystem of the plateau was distinct. An analysis of alpine vegetation under changes in climatic conditions was conducted in this study. This was done through an examination of vegetation greenness and its relationship with climate variability using the Advanced Very High Resolution Radiometer satellite imagery and climate datasets. Vegetation in the plateau experienced a positive trend in greenness, with 18.0 % of the vegetated areas exhibiting significantly positive trends, which were primarily located in the eastern and southwestern parts of the plateau. In grasslands, 25.8 % of meadows and 14.1 % of steppes exhibited significant upward trends. In contrast, the broadleaf forests experienced a trend of degradation. Temperature, particularly summer temperature, was the primary factor promoting the vegetation growth in the plateau. The wetter and warmer climate in the east contributed to the favorable conditions for vegetation. The alpine meadow was mostly sensitive to temperature, while the steppes were sensitive to both temperature and precipitation. Although a warming climate was expected to be beneficial to vegetation growth in the alpine region, the rising temperature coupled with reduced precipitation in the south did not favor vegetation growth due to low humidity and poor soil moisture conditions.     

GPS measurements (2003–2006) in the Sikhote Alin network,the Far East

This paper considers results of geodynamic studies using the GPS method in the territory of the Far East. GPS measurements using TRIMBLE-4700 geophones were launched along the Sikhote Alin profile in 2003. The technology of the GPS measurements and the problems of selecting the measurement sites and network configuration with reference to the region’s structure are discussed. The results of GPS measurements in 2003–2006 were used to study the fault system of the Far East continental margin. Different models of the Eurasia rotation (from the known NNR-NUVEL-1A to the recent ones) were analyzed. The solid-body rotation of Eurasia was predicted in the framework of the AR-IR-2006 model with a pole located at 51.045°N latitude, 255.842° longitude and rotating at a rate of 0.2423°/Ma. The parameters of the Amur plate rotation were preliminarily estimated (57.6° ± 0.5°N, 117.1 ± 0.5°E, and 0.083° ± 0.004°/m.y) using results on the Sikhote Alin and Transbaikalian network.     

Contrasting komatiite belts,associated Ni–Cu–(PGE) deposit styles and assimilation histories

The Agnew–Wiluna greenstone belt in the Yilgarn Craton of Western Australia is the most nickel-sulfide-endowed komatiite belt in the world. The Agnew–Wiluna greenstone belt contains two mineralised units/horizons that display very different volcanological and geochemical features. The Mt Keith unit comprises >500 m-thick spinifex-free adcumulate-textured lenses, which are flanked by laterally extensive orthocumulate-textured units. Spinifex texture is absent from this unit. Disseminated nickel sulfides, interstitial to former olivine crystals, are concentrated in the lensoidal areas. Massive sulfides are locally present along the base or margins of the lenses or channels. The Cliffs unit is locally >150 m thick and comprises a sequence of differentiated spinifex-textured flow units. The basal unit is the thickest, and contains basal massive nickel-sulfide mineralisation. The Mt Keith and Cliffs units display important common features: (i) MgO contents of 25–30% in inferred parental magmas; and (ii) Al/Ti ratios of ～20 (Munro-type). However, the Mt Keith unit is highly crustally contaminated (e.g. LREE-enriched, high HFSEs), whereas the Cliffs unit does not display evidence of significant crustal assimilation. We argue that the distinct trace-element concentrations and profiles of the two komatiite units reflect their different emplacement style and country rocks: the Mt Keith unit is interpreted to have been emplaced as an intrusive sill into dacitic volcanic units whereas the Cliffs unit was extruded as lava flow onto tholeiitic basalts in a subaqueous environment. The mode of emplacement and nature of country rock is the single biggest factor in controlling mineralisation styles in komatiites. On the other hand, evidence of crustal contamination does not necessarily provide information of the prospectivity of komatiites to host Ni–Cu–(PGE) mineralisation, despite being a good proxy for the style of komatiite emplacement and the nature of country rocks.     

Preliminary Study on the PGE Geochemistry of the Permian Basalts in the Jinping Area

INTRODUCTIONIn comparison with studies on the geochemistryof the REE and trace elements of the Emeishan Per-mian basalts ,there has been onlyli mited research onthe platinum group elements ( PGE) . Preli minarystudies have been carried out on the PGE geochemis-try of the basalts in the Emeishan area ( QingyingPower Station profile) and Xinjie area (Zhang andLi ,1998) ,andinthe Shuicheng and Weining areasinGuizhou (Li et al .,2003) . There are no PGEanaly-sis data of the basaltsin…     

Hydrothermal alteration and Cu–Ni–PGE mobilization in the charnockitic rocks of the footwall of the South Kawishiwi intrusion,Duluth Complex,USA

In the Neoarchean (~ 2.7 Ga) contact metamorphosed charnockitic footwall of the Mesoproterosoic (1.1 Ga) South Kawishiwi intrusion of the Duluth Complex, the primary metamorphic mineral assemblage and Cu–Ni–PGE sulfide mineralization is overprinted by an actinolite + chlorite + cummingtonite + prehnite + pumpellyite + quartz + calcite hydrothermal mineral assemblage along 2–3 cm thick veins. In calcite, hosted by the hydrothermal alteration zones and in a single recrystallized quartz porphyroblast, four different fluid inclusion assemblages are documented; the composition of these fluid inclusions provide p–T conditions of the fluid flow, and helps to define the origin of the fluids and evaluate their role in the remobilization and reprecipitation of the primary metamorphic sulfide assemblage.Pure CO₂ fluid inclusions were found as early inclusions in recrystallized quartz porphyroblast. These inclusions may have been trapped during the recrystallization of the quartz during the contact metamorphism of the footwall charnockite in the footwall of the SKI. The estimated trapping pressure (1.6–2.0 kbar) and temperature (810–920 °C) conditions correspond to estimates based on felsic veins in the basal zones of the South Kawishiwi intrusion.Fluid inclusion assemblages with CO₂–H₂O–NaCl and CH₄–N₂–H₂O–NaCl compositions found in this study along healed microfractures in the recrystallized quartz porphyroblast establish the heterogeneous state of the fluids during entrapment. The estimated trapping pressure and temperature conditions (240–650 bar and 120–150 °C for CO₂–H₂O–NaCl inclusions and 315–360 bar and 145–165 °C for CH₄–N₂–H₂O–NaCl inclusions) are significantly lower than the p–T conditions (> 700 °C and 1.6–2 kbar) during the contact metamorphism, indicating that this fluid flow might not be related to the cooling of the Duluth Complex and its contact aureole. The presence of chalcopyrite inclusions in these fluid inclusions and in the trails of these fluid inclusion assemblages confirms that at least on local scale these fluids played a role in base metal remobilization. No evidences have been observed for PGE remobilization and transport in the samples. The source of the carbonic phase in the carbonic assemblages (CO₂; CH₄) could be the graphite, present in the metasedimentary hornfelsed inclusions in the basal zones of the South Kawishiwi intrusion.The hydrothermal veins in the charnockite can be characterized by an actinolite + cummingtonite + chlorite + prehnite + pumpellyite + calcite (I–II) + quartz mineral assemblage. Chlorite thermometry yields temperatures around 276–308 °C during the earliest phase of the fluid flow. In the late calcite (II) phase, high salinity (21.6–28.8 NaCl + CaCl₂ equiv. wt.%), low temperature (90–160 °C), primary aqueous inclusions were found. Chalcopyrite (± sphalerite ± millerite), replacing and intersecting the early hydrothermal phases, are associated to the late calcite (II) phase. The composition of the formational fluids in the Canadian Shield is comparable with the composition of the studied fluid inclusions. This suggests that the composition of the fluids did not change in the past 2 Ga and base metal remobilization by formational fluids could have taken place any time after the formation of the South Kawishiwi intrusion.Sulfur isotope studies carried out on the primary metamorphic (δ³⁴S = 7.4–8.9‰) and the hydrothermal sulfide mineral assemblage (δ³⁴S = 5.5–5.7‰) proves, that during the hydrothermal fluid flow the primary metamorphic ores were remobilized.