Massive Sulfide Ore Research Articles

Relics of near-bottom fauna in massive sulfide ores

The additional study of ancient volcanogenic massive sulfide deposits in various regions revealed microtextures, probably of biogenic origin, which could represent varieties of the shells of mineralized fauna. The new finds expand the list of sites containing relics of bioforms associated with hydrothermal vents of "black smokers".

A 3D forward-modeling approach for airborne electromagnetic data using a modified spectral-element method

The spectral-element (SE) method, which is based on the Galerkin technique, has been gradually implemented in geophysical electromagnetic (EM) 3D simulation. The accuracy and efficiency of this approach, implemented for deformed hexahedral and regular meshes, has been verified for airborne EM forward modeling. One advantage of the SE method over the conventional finite-element method is that it provides accurate results for earth models that can be adequately parameterized using a coarse mesh. However, realistic models can contain important small-scale conductivity variations or larger features with complicated boundaries. To overcome the limitations imposed by using the same mesh to parameterize the model and for implementing the forward-modeling approach, we have developed an adaptation of the conventional SE method. This is inspired by the ideas behind the element-free Galerkin (EFG) method, in which the conductivity is no longer assumed to be constant within a cell; instead, it is handled via the same kind of numerical integration as in the EFG method. This allows a coarse, regular hexahedral mesh to be used for the forward modeling for complex earth models. After presenting the theory for this new SE approach, we test it for airborne EM modeling of 1D and 3D models to verify its flexibility and accuracy. Finally, we model the Ovoid Zone massive sulfide ore body located at Voisey’s Bay, Labrador, Canada, to illustrate the flexibility and practicality of our approach.

Pb-Nd-Sr Isotope Geochemistry of Metapelites from the Iberian Pyrite Belt and Its Relevance to Provenance Analysis and Mineral Exploration Surveys

Abstract The Iberian Pyrite Belt is a world-class metallogenic district developed at the Devonian-Carboniferous boundary in the Iberian Variscides that currently has seven active mines: Neves Corvo (Cu-Zn-Sn) and Aljustrel (Cu-Zn) in Portugal, and Riotinto (Cu), Las Cruces (Cu), Aguas Teñidas (Cu-Zn-Pb), Sotiel-Coronada (Cu-Zn-Pb), and La Magdalena (Cu-Zn-Pb) in Spain. The Iberian Pyrite Belt massive sulfide ores are usually hosted in the lower sections of the volcano-sedimentary complex (late Famennian to late Visean), but they also occur in the uppermost levels of the phyllite-quartzite group at the Neves Corvo deposit, stratigraphically below the volcano-sedimentary complex. A Pb-Nd-Sr isotope dataset was obtained for 98 Iberian Pyrite Belt metapelite samples (from Givetian to upper Visean), representing several phyllite-quartzite group and volcano-sedimentary complex sections that include the footwall and hanging-wall domains of ore horizons at the Neves Corvo, Aljustrel, and Lousal mines. The combination of whole-rock Nd and Sr isotopes with Th/Sc ratios shows that the siliciclastic components of Iberian Pyrite Belt metapelites are derived from older quartz-feldspathic basement rocks (–11 ≤ εNdinitial ≤ –8 and (87Sr/86Sr)i up to 0.727). The younger volcano-sedimentary complex metapelites (upper Tournaisian) often comprise volcanic-derived constituents with a juvenile isotopic signature, shifting the εNdi up to +0.2. The Pb isotope data confirm that the phyllite-quartzite group and volcano-sedimentary complex successions are crustal reservoirs for metals found in the deposits. In Neves Corvo, where there is more significant Sn- and Cu-rich mineralization, the higher (206Pb/204Pb)i and (207Pb/204Pb)i values displayed by phyllite-quartzite group and lower volcano-sedimentary complex metapelites (up to 15.66 and 18.33, respectively) suggest additional contributions to the metal budget from a deeper and more radiogenic source. The proximity to Iberian Pyrite Belt massive sulfide ore systems hosted in metapelite successions is observed when (207Pb/204Pb)i >15.60 and Fe2O3/TiO2 or (Cu+Zn+Pb)/Sc >10. These are important criteria that should be considered in geochemical exploration surveys designed for the Iberian Pyrite Belt.

Porphyry Cu mineralization processes of Xinqiao deposit, Tongling ore district: Constraints from the geochronology and geochemistry of zircon, apatite, and rutile

Xinqiao is a large ore deposit that is well known for its stratabound massive sulfide and skarn ores. Recently, deep drilling has shown that Xinqiao also has typical porphyry mineralization and alteration features. The Cu grade is 0.3–0.6% and occurs as quartz-pyrite-chalcopyrite in potassic and phyllic alteration zones. The characteristics and genetic processes of the porphyry mineralization at Xinqiao have not previously been reported.Three intrusion types are recognized; pyroxene diorite, quartz diorite and quartz monzodiorite porphyry; Cu mineralization is associated with the quartz diorite and quartz monzodiorite porphyry. Zircon U-Pb dating shows that the three intrusions were all emplaced at about 140 Ma. Zircons from the quartz diorite and quartz monzodiorite porphyry show higher Ce4+/Ce3+ and Eu/Eu* (>0.5), 10,000(Eu/Eu*)/Y (>5), and (Ce/Nd)/Y (>0.01), than the pyroxene diorite, and apatites from the mineralized intrusions have slightly higher SO3 (average 0.40) contents than ones from the pyroxene diorite (average 0.33). These results indicate that the fertile magmas were more oxidized, hydrous, and S-rich than the barren pyroxene diorite, consistent with their association with porphyry Cu mineralization. U-Pb dating of hydrothermal rutile from the porphyry mineralization and garnet from the skarn ore both yield ages of about 140 Ma, suggesting that the porphyry and skarn mineralization belong to same system. The geochemistry of hydrothermal rutile and apatite in the porphyry mineralization zone also indicates that Xinqiao ores were produced from a S-rich magmatic-hydrothermal fluid system. Our results highlight huge porphyry Cu mineralization potential beneath stratabound and skarn deposits in the Middle-Lower Yangtze River metallogenic belt.

Metallogeny of a Pan-African oceanic arc: VHMS and gold deposits in the Ariab-Arbaat belt, Haya terrane, Red Sea Hills (Sudan)

Gold in the Ariab district (Red Sea Hills, Sudan) is mined in gossans developed over volcanogenic massive sulphide (VHMS) deposits formed in the context of a Tonian ensimatic arc of the Haiya terrane, in the Neoproterozoic Arabo-Nubian Shield. All the primary gold occurrences of the Ariab belt, whatever their style (VHMS-, quartz lode- or shear-zone-hosted), appear, however, to have been syn-to late-kinematic, i.e., formed in the context of the final Pan-African collision leading to the Arabian-Nubian Shield (D3 event), and therefore are post-VHMS. Gold is thus found associated with either galena or bismuth telluride in late syn- to post-metamorphic sets of (micro)cracks, mostly within earlier pyrite or arsenopyrite. Gold deposition as native gold or electrum occurred when an intense fluid circulation of metamorphic CO2-H2O rich fluids underwent significant decompression from lithostatic to hydrostatic pressures at temperatures decreasing from 400 to 430 °C at around 8 km depth down to 300 °C. Although no clear evidence of volatile unmixing was observed, the decompression, together with a temperature decrease due to dilution by aqueous rich fluids, favoured gold deposition.The late-D3 gold event in the Ariab belt has all the makings of an orogenic gold system, notably similar to the Late Carboniferous gold event in the West European Variscan belt. Thus, it is possible to propose that, at the end of the collision events, fluids released from the newly formed terrane root were channelled towards the upper crust through the major D3 shear zones such as the Oko shear zone. The fluids outpouring from these major drains were then conveyed through fault plays and damaged zones, up to specific chemical traps within massive sulphide ore bodies or quartz veins systems. Thus, the Ariab gold district could be classified as a representative of the class of orogenic gold deposits.

GEOLOGY, MINERAL COMPOSITION OF ORE AND ALTERED HOST ROCKS OF MASSIVE SULPHIDE MINERALIZATION OF THE AKZHARSKY ORE FIELD (SOUTH URALS)

The article describes the geological structure of the Akzharsky ore field, of five individual massive sulphide mineralization: Yuzhnoye, Yuzhno-Akzharskoye, Novoye, Bezymyannoye and Burozheleznyakovoye. The results of a microscopic study of the mineral composition of ores and altered host rocks are discussed. It is shown that all ore mineralizations are concentrated at a single lithological-stratigraphic level, but differ from each other in details of the structure, scale and mineral composition of mineralization. Massive ores prevail, and embedded and densely embedded ores are subordinate. The composition of the ore is mainly chalcopyrite-pyrite, to a lesser extent sphalerite-chalcopyritepyrite and pyrite. In the direction from south to north of the ore field, there is a change in the direction of increasing «polymetallicity» in ore mineralogy. Texture and structure of the ores of the Akzharsky ore field are rather uniform. Linear structures predominate (from banded to schistosely banded). Massive structures have a sharply subordinate distribution; brecciated ones are noted in isolated cases. Hydrothermal alterations formed mainly in rhyodacite-basalt strata from foot wall of ore bodies and, according to mineral composition, belong to propylites. They are characterized by an unstable set of mineral facies, weak contrast of metasomatic zones, and extremely uneven of rocks alteration. It has been established that the volcanic complexes of the ore field contain deposits not typical for the Ural massive sulphide ore province, differing in the mineral composition of ores, the conditions of their geological setting and the nature of the rocky alterations. This made it possible to concretize the concept of the relationship between the considered mineralization and volcanism and significantly supplement the already known typical models of pyrite-bearing ore-magmatic systems.

Structural controls on the localization of the mineralized Copper Cliff embayment and the Copper Cliff Offset dyke, Sudbury Igneous Complex, Canada

The Main Mass of the Sudbury Igneous Complex (SIC) is a 1.5–5 km thick, layered sheet of impact melt rocks, intensely studied because of the magmatic Ni-Cu-PGE sulfide deposits associated with the base of the Main Mass and connected dykes, known as the Sublayer and Offset dykes, respectively. The mode of emplacement of the mineralized Offset dykes that connect to the Main Mass through morphologic crater-floor irregularities (embayments) and the style of post-cratering deformation that affected the Offset dykes is not fully understood. This field-based study of the Copper Cliff Embayment (CCE) and Offset (CCO) dyke contributes to unraveling the mode of melt emplacement and the role of pre-impact faults in the deformation of the southern SIC. Field relationships indicate that the CCO dyke formed before the CCE and Sublayer were chemically fully evolved. Respective melts were injected into footwall rocks weakened by pre-impact deformation and cratering as a protracted event, with barren quartz diorite (QD) emplaced prior to mineralized, inclusion-bearing quartz diorite (IQD). Massive sulfide ore bodies appear to have formed late in the evolution of the dyke and physical separation (decoupling) of silicate magma and sulfide melt is required. NW-SE-shortening folded and faulted the strata hosting the CCO dyke and deformation was facilitated through re-activated E-W-striking, pre-impact faults. Restoring the initial geometry of the dyke and embayment, using 3D modelling and field constraints, helped to refine total slip estimates along major faults and confirmed that melts migrated gravitationally downward into the CCO dyke.

The Solution Interaction of Tetrathionate Ions and Sodium Isobutyl Xanthate and Its Effect on the Flotation of Galena and Chalcopyrite

Tetrathionates have been found in significantly high concentrations in recycled process waters from massive sulphide ore processing plants. These polythionates react with xanthate added to flotation pulps thus reducing xanthate dosages in solution potentially affecting flotation performance. The current study focused on the effect of the tetrathionate-xanthate reaction on sulphide mineral recoveries. Ore dissolution studies confirmed the generation of tetrathionates by copper-lead-zinc ores. In 20 min, the tetrathionates consumed more than half of the xanthate in solution at pH 7. Rest potential measurements and Fourier transform infrared spectroscopy (FTIR) showed that the degree of collector-mineral interactions of xanthate and both galena and chalcopyrite was greatly reduced in the presence of a 2000 mg/L tetrathionate solution. Microflotation tests showed that chalcopyrite recovery was less sensitive to tetrathionates as indicated by small changes in mineral recoveries. Galena was sensitive to the action of tetrathionates on the mineral surface as the galena recovery significantly declined when floated with xanthate as a collector in both a 500 mg/L tetrathionate solution and a 2000 mg/L tetrathionate solution. These fundamental results lay a sound base on which more discussion into the significance and the effect of tetrathionates on flotation performance of sulphide ores can be developed.

Flotation of Seafloor Massive Sulfide Ores: Combination of Surface Cleaning and Deactivation of Lead-Activated Sphalerite to Improve the Separation Efficiency of Chalcopyrite and Sphalerite

The purpose of this study is to propose the flotation procedure of seafloor massive sulfide (SMS) ores to separate chalcopyrite and galena as froth and sphalerite, pyrite, and other gangue minerals as tailings, which is currently facing difficulties due to the presence of water-soluble compounds. The obtained SMS ore sample contains CuFeS2, ZnS, FeS2, SiO2, and BaSO4 in addition to PbS and PbSO4 as Pb minerals. Soluble compounds releasing Pb, Zn2+, Pb2+, and Fe2+/3+ are also contained. When anglesite co-exists, lead activation of sphalerite occurred, and thus sphalerite was recovered together with chalcopyrite as froth. To remove soluble compounds (e.g., anglesite) that have detrimental effects on the separation efficiency of chalcopyrite and sphalerite, surface cleaning pretreatment using ethylene diamine tetra acetic acid (EDTA) was applied before flotation. Although most of anglesite were removed and the recovery of chalcopyrite was improved from 19% to 81% at 20 g/t potassium amyl xanthate (KAX) after EDTA washing, the floatability of sphalerite was not suppressed. When zinc sulfate was used as a depressant for sphalerite after EDTA washing, the separation efficiency of chalcopyrite and sphalerite was improved due to deactivation of lead-activated sphalerite by zinc sulfate. The proposed flotation procedure of SMS ores—a combination of surface cleaning with EDTA to remove anglesite and the depression of lead-activated sphalerite by using zinc sulfate—could achieve the highest separation efficiency of chalcopyrite and sphalerite; that is, at 200 g/t KAX, the recoveries of chalcopyrite and sphalerite were 86% and 17%, respectively.

Nd and Hf isoscapes of the Yilgarn Craton, Western Australia and implications for its mineral systems

The Yilgarn Craton, Western Australia is endowed with significant gold, nickel‑copper, Cu-Pb-Zn volcanic-hosted massive sulphide (VHMS) and iron ore deposits. Detailed knowledge of the spatial relationships between mineral systems and the crustal framework of the Yilgarn Craton may be powerful tools in the predictive exploration of undiscovered mineral systems. Both Nd and Hf isotopes have the potential to image crustal residence, mantle tapping structures, and juvenile input over both space and time. This study uses a recent compilation of Hf (1236 zircon analyses) and Nd (462 whole rock analyses) isotopes to image the architecture of the crust and compare this to the distribution of gold, nickel‑copper-platinum group elements (Ni-Cu-PGEs), Cu-Pb-Zn VHMS and iron ore deposits. Spatial correlation plots reveal a statistically significant relationship between Nd and Hf isotopic domains and the occurrence of gold, Ni-Cu-PGE, base metals, and iron confirmed by the coefficient of determination (R2) which measures how differences in metal occurrences can be explained by differences in the isotopic signature. Nickel occurrences show the strongest antithetic spatial correlation (R2 = 0.80) with Hf model ages, followed by gold (R2 = 0.58) and base metals (R2 = 0.35), which implies higher metal endowment in areas of more juvenile crust. In contrast, there is a significant positive spatial correlation (R2 = 0.49) between iron ore occurrence and older model ages. Isotopic data can also be plotted as Hf or Nd time-slices, where the strongest spatial correlation between gold, nickel, and base metal occurrence and juvenile input occurs at ca. 2700–2550 Ma. Generally, a model can be proposed where (1) base metals are more prevalent in juvenile crust because of its thinner nature, greater mantle input, high-heat flow, increased water-magma interaction; (2) iron ore is concentrated in regions of old, mature, and stable crust; (3) komatiite-hosted Ni-Cu-PGE systems are focused in juvenile rift zones at the edge of old crustal blocks; and (4) gold is also localised in juvenile crust at craton edges where several factors are localised, including orogenesis, occurrence of previously fertilised crust (i.e. Fe-rich lithologies, sanukitoids), favourable structures (potential inversion of rift structures), and ‘late’ alkaline magmatism. In gold, Ni-Cu-PGE, and base metal mineral systems, the ability of magmas to access higher crustal levels unimpeded appears vital in regional prospectivity and is itself a function of crustal configuration.

The Haidbach deposit in the Central Tauern Window, Eastern Alps, Austria: a metamorphosed orthomagmatic Ni-Cu-Co-PGE mineralization in the Polymetallic Ore District Venediger Nappe System – Hollersbach Complex

Abstract Cu-Ni-Co-PGE mineralization occurs at Haidbachgraben in the Early Palaeozoic, Subpenninic Hollersbach Complex of the Central Tauern Window, Austria. Massive sulfide ore formed from sulfide melt segregated from silicate melt during intrusion of pyroxenite into magmatic rocks formed in an MORB-type environment. Relics of magmatic minerals include chromian spinel and polyphase sulfide droplets composed of pyrrhotite, chalcopyrite and pentlandite preserved in recrystallized pyrite. Both ore and host rocks were multiply deformed and metamorphosed, leading to hornblendite carrying the ore, enveloped by chlorite-epidote schist. Conditions of – likely Variscan – amphibolite facies metamorphism are documented by relict pargasitic cores in hornblende and actinolite-tremolite, and by ternary sulfarsenide compositions in the Co-Ni-Fe solid solution series that are the most common accessory minerals found in the sulfide ore. Pyrrhotite, pentlandite, chalcopyrite and pyrite are the major sulfide minerals. Chalcopyrite is Cd-rich and retains a high-temperature magmatic signature. High Co/Sb and moderate Se/As ratios in pyrite also point to a magmatic environment of mineralization. The accessory mineral assemblage of small grain size (mostly <10 µm) comprises native Au-Ag alloy and petzite as Au-Ag minerals, sperrylite, a variety of Pd tellurides and bismuthotellurides with elevated Sb, irarsite, and Re sulfides such as tarkianite and a Pb-Re sulfide. In addition, minor molybdenite, bournonite, scheelite and selenides have been identified. Two precious metal assemblages are present in individual samples: (1) hessite associated with Pd tellurides, often accompanied by sphalerite and chalcopyrite; (2) tarkianite forming euhedral inclusions in pyrite. Sperrylite and Au-Ag native alloys are present throughout and were also detected in silicate matrix. Most of the precious metal-bearing phases must have formed during recrystallization of base metal sulfides after the magmatic, and probably during later metamorphic events terminating in the Neoalpine Tauern crystallization.

New Geochemical and Mineralogical Data on Rocks and Ores of the NE Flank of the Oktyabr’skoe Deposit (Norilsk Area) and a View on Their Origin

The Oktyabr’skoe deposit in the Norilsk ore district is the largest platinum-copper-nickel deposit in the world. It contains a huge main orebody (2.4 km3) of massive sulfide ores and some smaller sulfide bodies. Almost all publications on this deposit are devoted to the main orebody. However, to solve the problems of the deposit genesis, it is necessary to take into account the geological structure of the entire area and the composition of all orebodies. For the first time we present data on the inner structure, geochemical and mineralogical characteristics of the intrusive body, and related the disseminated and massive sulfide ores (orebody number C-5) in the northeastern flank of the deposit. The intrusion studied in the core of the borehole RG-2 consists of several horizons including the following rock varieties (from bottom to top): olivine gabbro-dolerites, taxitic gabbro-dolerites, picritic gabbro-dolerites, troctolites, olivine-free gabbro-dolerites, ferrogabbro, and leucogabbro. The intrusion shows a strong differentiated inner structure where high-Mg rocks (up to 25 wt.% MgO troctolites and picritic gabbro-dolerites) in the bottom are associated with low-Mg rocks (6–7 wt.%, gabbro-dolerites, leucogabbro, ferrogabbro) without intermediate differentiated members (8–12 wt.% MgO olivine gabbro-dolerites). Rocks are characterized by low TiO2 content (≤1 wt.%). Taxitic gabbro-dolerites, picritic gabbro-dolerites, and troctolites contain disseminated sulfide chalcopyrite-pyrrhotite mineralization (32 m thick). Cu and Ni concentrations reach up 0.74 and 0.77 wt.%, respectively. Massive ores (27 m) occur in the bottom part of the intrusion. The ores consist of pentlandite, chalcopyrite and pyrrhotite, the latter mineral dominates. Their chemical composition is stable: Cu/Ni ~1, Pd/Pt varies from 5 to 6. The C-5 orebody is similar to the C-3 orebody in terms of mineral and chemical compositions, and differ from the nearby the C-4 orebody which is characterized by a Cu/Ni ratio changing from 5 to 8. On the basis of geochemical and mineralogical data, it is assumed that orebodies C-3 and C-5 are associated with one intrusion, while the orebody number C-4 is related to another intrusive body. Thus, the deposit has a more complex structure and includes several more intrusions than is usually considered.

The Mineral Composition of Paleoproterozoic Metamorphosed Massive Sulfide Ores in the Kola Region (A Case Study of the Bragino Ore Occurrence, Southern Pechenga)

Many massive sulfide ore occurrences and deposits in the Kola region are located within the Paleoproterozoic Pechenga–Imandra–Varzuga rift belt (2.5–1.7 Ga). They are hosted by volcanosedimentary complexes of the South Pechenga (Bragino ore occurrence) and western Imandra–Varzuga structural zones (Pirrotinovoe Ushchel’e deposit, Tahtarvumchorr ore occurrence, etc.). The age of the massive sulfide ore was estimated at ca. 1.9 Ga. The ores and their host complexes underwent amphibolite-facies metamorphism, which accounts for their specific mineral composition. The types of ores in the Bragino ore occurrence are discussed, the mineral assemblages are listed, and the major ore minerals, that is, pyrrhotite, pyrite, sphalerite, marcasite, etc., are characterized.

Constraints on scheelite genesis at the Dabaoshan stratabound polymetallic deposit, South China

Abstract The genesis of the Dabaoshan stratabound base metal deposit has remained in dispute since its discovery. Scheelite is commonly present in both the Cu-S orebody and adjacent porphyry-style Mo-W mineralization and can provide insights into the hydrothermal history. In the stratabound Cu-S orebodies, there are three stages of mineralization: early-stage, Cu-(W), and late-stage. Two types of scheelite (here referred to as SchA and SchB) are identified in the Cu-(W) mineralization stage. SchA is anhedral and disseminated in massive sulfide ores. It coexists with chalcopyrite and replaces the preexisting arsenic-bearing pyrite. SchA exhibits chaotic cathodoluminescent (CL) textures and contains abundant mineral inclusions, including pyrite, chalcopyrite, arsenopyrite, uraninite, and minor REE-bearing minerals. Chemically, SchA displays middle REE (MREE)-enriched patterns with negative Eu anomalies. SchB occurs in veins crosscutting the stratabound orebodies and shows patchy textures in CL images. Based on CL texture, SchB is subdivided into SchB1 and SchB2. SchB1 is CL-dark and occasionally shows oscillatory zoning, whereas SchB2 is CL-bright and relatively homogeneous. Chemically, SchB1 has a high-U content (mean = 552 ppm) and REE patterns varying from MREE-enriched to MREE-depleted. In contrast, SchB2 is depleted in U (mean = 2.5 ppm) and has MREE-enriched patterns. Compared with SchB, SchA is significantly enriched in Ba. Scheelite in the stratabound orebodies has similar Y/Ho ratios and trace-element characteristics as Sch3 in the Dabaoshan porphyry system. In situ U-Pb dating of hydrothermal apatite, collected from the Sch3-bearing veins in the footwall of stratabound orebodies, yielded a mineralization age of 160.8 ± 1.1 Ma. Zircon from the Dabaoshan granite porphyry yielded a U-Pb age of 161.8 ± 1.0 Ma. These two ages are consistent within uncertainty, suggesting that the ore-forming fluid responsible for tungsten mineralization in the stratabound orebodies was derived from the porphyry system. When fluid emanating from the deep porphyry system encountered the overlying Lower Qiziqiao Formation and stratabound orebodies, replacement reactions resulted in dramatic variations in physiochemical conditions (e.g., decrease in fO2, increase in Ca/Fe, As, Ba). During this process, U6+ was reduced to U4+, and As and Ba were leached out of the preexisting pyrite and host rock. Fluid-rock interactions triggered a rapid discharge of fluids, forming SchA with chaotic CL textures and abundant inclusions, but uniform REE patterns. SchB (characterized by patches with different chemical characteristics) may have been formed from repeated injection of ascending fluids into fractures crosscutting the preexisting massive sulfide ores. We propose that Jurassic porphyry Mo-W mineralization contributed to tungsten mineralization in the stratabound orebodies. Considering that Cu and W mineralization are genetically related, not only in the footwall but also in the stratabound orebodies, we infer that Cu in the stratabound orebodies was locally sourced from the Jurassic porphyry mineralization.

Geology and Genesis of the Giant Gorevskoe Pb-Zn-Ag Deposit, Krasnoyarsk Territory, Russia

Abstract The Gorevskoe Pb-Zn-Ag mine is currently the largest producer of Pb and Zn in Russia, exploiting one of the largest sediment-hosted Pb-Zn deposits worldwide. Despite its size and economic importance, the Gorevskoe deposit remains poorly understood. It is located on the western margin of the Siberian craton within the Yenisei Ridge, a Neoproterozoic orogenic belt. Mineralization consists of three tabular orebodies that are in turn composed of multiple stacked stratiform to strata-bound lenses of galena-pyrrhotite-sphalerite-rich massive sulfide ore, hosted in organic-rich marine metalimestones and calcareous slates of Stenian to Tonian age (1,020 ± 70 Ma). Extensive Fe-Mg-Mn-carbonate alteration haloes surround the ore lenses. The Pb isotope signature of the deposit is consistent with derivation of Pb, and probably all associated metals, from an evolved crustal source at the time of formation of the host rocks. The sulfur isotope compositions of pyrrhotite, sphalerite, galena, arsenopyrite, and pyrite (δ34S = 16.0–20.4‰) do not vary considerably across the deposit and are within the range reported for contemporaneous seawater, indicating complete reduction of marine sulfate as the main source of sulfur. The available geologic and geochemical data indicate that the Gorevskoe deposit belongs to the sediment-hosted massive sulfide (SHMS) class of Zn-Pb deposits, with an affinity to Selwyn-type deposits. Hydrothermal mineralization appears to be temporally related to rifting and distal mafic volcanism in a passive margin setting. Geologic relationships suggest that the orebodies formed in a diagenetic environment. Furthermore, the predominance of primary pyrrhotite over pyrite as the major iron sulfide, the presence of abundant siderite, and the relatively homogeneous sulfur isotope signature of the ores indicate highly reducing conditions during ore formation. They also constrain the character of the metal-bearing fluid to be similarly reducing, and of moderate temperature (200°–300°C). Gorevskoe may thus be regarded as one of the world’s largest Selwyn-type SHMS deposits.

Coulsonite FeV2O4—A Rare Vanadium Spinel Group Mineral in Metamorphosed Massive Sulfide Ores of the Kola Region, Russia

This work presents new data on a rare vanadium spinel group mineral, i.e., coulsonite FeV2O4 established in massive sulfide ores of the Bragino occurrence in the Kola region, Russia. Coulsonite in massive sulfide ores of the Bragino occurrence is one of the most common vanadium minerals. Three varieties of coulsonite were established based on its chemical composition, some physical properties, and mineral association: coulsonite-I, coulsonite-II, and coulsonite-III. Coulsonite-I forms octahedral crystal clusters of up to 500 µm, and has a uniformly high content of Cr2O3 (20–30 wt.%), ZnO (up to 4.5 wt.%), and MnO (2.8 wt.%), high microhardness (743 kg/mm2) and coefficient of reflection. Coulsonite-II was found in relics of quartz–albite veins in association with other vanadium minerals. Its features are a thin tabular shape and enrichment in TiO2 of up to 18 wt.%. Coulsonite-III is the most common variety in massive sulfide ores of the Bragino occurrence. Coulsonite-III forms octahedral crystals of up to 150 µm, crystal clusters, and intergrowths with V-bearing ilmenite, W-V-bearing rutile, Sc-V-bearing senaite, etc. Chemical composition of coulsonite-III is characterized by wide variation of the major compounds—Fe, V, Cr. In some crystals of coulsonite-III, relics of chromite are observed. The microhardness of coulsonite-III is 577 kg/mm2, the reflection coefficient changes in relation to iron, vanadium, and chromium content.

Magnetite Chemistry by LA-ICP-MS Records Sulfide Fractional Crystallization in Massive Nickel-Copper-Platinum Group Element Ores from the Norilsk-Talnakh Mining District (Siberia, Russia): Implications for Trace Element Partitioning into Magnetite

Abstract 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.

Differentiated Mafic–Ultramafic Intrusions of the Zubovsky Type in the Norilsk Area: Petrochemistry, Geochemistry, and Ore Potential

Intrusions of the Zubovsky type (1) are commonly dominated by troctolite in their ultramafic parts and have an insignificant number (if any) of ultramafic units; (2) occur among olivine and olivine-bearing gabbro-dolerites and often show evidence of a number of accumulation of cumulus olivine, (3) have weakly pronounced (if any) taxitic gabbrodolerite units; (4) include widespread leucocratic hybrid-metasomatic rocks and hybrid quartz- and cordierite-bearing norites and gabbronorites at contacts with the host aluminosilicate rocks; and (5) generally have a low ore content, with the prevalence of disseminated ore units among troctolites and ultramafic rocks, and almost complete absence of massive sulfide ores. The paper is the first to present data on the composition and Nd–Sr–Cu–S isotope-geochemical characteristics of rocks and sulfide ores from the Zubovsky-type intrusions in the Norilsk area. The silicate material of the Zub-Marksheider and Vologochan intrusions is characterized by similar Nd–Sr isotopic parameters: eNd = –1.2 ± 0.5, (87Sr/86Sri) = 0.70685 ± 0.00127, and eNd = 1.2 ± 0.8, (87Sr/86Sri) = 0.70634 ± 0.00068, respectively. These parameters are close to those of intrusions accompanied by economic ore mineralization in the Norilsk area. The whole-rock samples generally have a more ‘radiogenic’ Nd isotopic composition than that of the pyroxene and plagioclase and less ‘radiogenic’ than that of the olivine. The highest eNd value (ca. 5.3) of the olivine indicates that depleted mantle (DM) material was involved in the magma-generating processes. Copper–sulfur isotope data for sulfide ores of the Zub-Marksheider and Vologochan intrusions are remarkably different: δ34S = 1.3 ± 2.3‰, δ65Cu = –0.1 ± 0.15‰ and δ34S = 7.0 ± 1.2‰, δ65Cu = –0.7 ± 0.3‰, respectively. The Cu isotope composition of the sulfide mineralization of both intrusions is close to that of massive and disseminated sulfide ores from the Talnakh deposit in the Norilsk area. The sulfur isotope data suggest that the host rocks had little effect on sulfide mineralization. The identified Nd–Sr–S–Cu isotope-geochemical parameters of the rocks and ores are an important indicator of the potential for rich PGE–Cu–Ni sulfide ores.

Pyrite Varieties at Pobeda Hydrothermal Fields, Mid-Atlantic Ridge 17°07′–17°08′ N: LA-ICP-MS Data Deciphering

The massive sulfide ores of the Pobeda hydrothermal fields are grouped into five main mineral microfacies: (1) isocubanite-pyrite, (2) pyrite-wurtzite-isocubanite, (3) pyrite with minor isocubanite and wurtzite-sphalerite microinclusions, (4) pyrite-rich with framboidal pyrite, and (5) marcasite-pyrite. This sequence reflects the transition from feeder zone facies to seafloor diffuser facies. Spongy, framboidal, and fine-grained pyrite varieties replaced pyrrhotite, greigite, and mackinawite “precursors”. The later coarse and fine banding oscillatory-zoned pyrite and marcasite crystals are overgrown or replaced by unzoned subhedral and euhedral pyrite. In the microfacies range, the amount of isocubanite, wurtzite, unzoned euhedral pyrite decreases versus an increasing portion of framboidal, fine-grained, and spongy pyrite and also marcasite and its colloform and radial varieties. The trace element characteristics of massive sulfides of Pobeda seafloor massive sulfide (SMS) deposit are subdivided into four associations: (1) high temperature—Cu, Se, Te, Bi, Co, and Ni; (2) mid temperature—Zn, As, Sb, and Sn; (3) low temperature—Pb, Sb, Ag, Bi, Au, Tl, and Mn; and (4) seawater—U, V, Mo, and Ni. The high contents of Cu, Co, Se, Bi, Te, and values of Co/Ni ratios decrease in the range from unzoned euhedral pyrite to oscillatory-zoned and framboidal pyrite, as well as to colloform and crystalline marcasite. The trend of Co/Ni values indicates a change from hydrothermal to hydrothermal-diagenetic crystallization of the pyrite. The concentrations of Zn, As, Sb, Pb, Ag, and Tl, as commonly observed in pyrite formed from mid- and low-temperature fluids, decline with increasing crystal size of pyrite and marcasite. Coarse oscillatory-zoned pyrite crystals contain elevated Mn compared to unzoned euhedral varieties. Framboidal pyrite hosts maximum concentrations of Mo, U, and V probably derived from ocean water mixed with hydrothermal fluids. In the Pobeda SMS deposit, the position of microfacies changes from the black smoker feeder zone at the base of the ore body, to seafloor marcasite-pyrite from diffuser fragments in sulfide breccias. We suggest that the temperatures of mineralization decreased in the same direction and determined the zonal character of deposit.

Setting, sulfur isotope variations, and metamorphism of Jurassic massiveZn‐Pb‐Agsulfide mineralization associated with arc‐type volcanism (Skra, Vardar zone, Νorthern Greece)

AbstractMassive Zn‐Pb‐Ag sulfide mineralization appears conformable with felsic volcanism, developed in an Upper Jurassic volcanic arc to the Southwest (SW) of the Serbo‐Macedonian continent in Northern Greece. The host volcanic sequence of the mineralization comprises mylonitized rhyolitic to rhyodacitic lavas, pyroclastics, quartz‐feldspar porphyries, and cherty tuffs. A “white mica—quartz—pyrite” mineral assemblage characterizes the volcanic rocks in the footwall and hanging‐wall of massive sulfide ore layers, formed as a result of greenschist‐grade regional metamorphism on “clay‐quartz‐pyrite” hydrothermal alteration haloes. Massive ore lenses are usually underlain by deformed Cu‐pyrite and quartz‐pyrite stockworks. Most of the sulfide ore bodies have proximal‐type features. Ductile deformation and regional metamorphism have transformed many of the stockwork structures. The mineralization is characterized by high Zn, Pb, and Ag contents, while Cu and critical metals are low. Primary depositional textures, for example, layering, clastic pyrite, colloform, and atoll textures were identified. The overall textural features of the mineralization indicate it has undergone mechanical deformation. The most prominent features of the effects of metamorphism, folding and shearing, are modification of the ore body morphology toward flattened and boudinage structures and transformation of the ore textures toward the dominance of planar fabrics. Sulfur isotope analyses of sulfides along with textural observations are consistent with a dual source of sulfide sulfur. Sulfur isotope values for sphalerite, non‐colloform pyrite, galena, and chalcopyrite fall in a limited range from −1.6 to +4.8‰ (mean δ34S + 2‰), indicating a hydrothermal source derived from the reduction of coeval seawater sulfate in the convective system. Pyrites with colloform and atoll textures are characterized by a34S depletion, indicating a bacterial reduction of coeval seawater sulfate. The morphology of ore beds, the mineralogy, sulfide textures, and ore chemistry along with the petrology and tectonic setting of the host rocks can be attributed to typical of a bimodal‐felsic metallogenesis. Although similar in many respects to classic Kuroko‐type volcanogenic massive sulfide mineralization, it has some atypical features, like the absence of barite ore, which is possibly a result of significant temporal depletion in sulfate due to bacterial reduction, a conclusion supported by the widespread occurrence of colloidal and atoll textures of pyrite.