Se and In minerals in the submarine oxidation zone of a massive sulfide orebody of the molodezhnoe copper–zinc massive sulfide deposit,Southern Urals

For the first time, extremely high Se and In contents were determined for the pinches of massive sulfide orebodies that are composed of small-clastic layered sulfide sediments transformed during submarine supergenesis. Se (clausthalite and naumannite) and In (roquesite) minerals were found. Hydrothermal chalcopyrite, a significant amount of which is present in the clasts of paleohydrothermal black smoker chimneys, was the source of Se. Most of the amount of In was contributed during dissolution of clasts of hydrothermal sphalerite, which is unstable in the submarine oxidation zone in the presence of oxidized pyrite.     

Subvolcanic gabbro–porphyrite and intrusive diorite,and sulfide mineralization of the Dzhusa volcanogenic massive sulfide deposit (Southern Urals)

Two sequentially formed groups of dikes in the gabbro–porphyrite complex have been distinguished, the ages of which are early Eifelian (early dikes) and early Givetian (late dikes). We have estimated the temperature impact of ore contact metamorphism, which is related to dikes of the Lower Carboniferous Magnitogorsk intrusive complex. A hidden zonality of microimpurities in the ore-forming minerals has been established for the first time by the LA-ICP-MS method. The ore formation age has been determined as early Eifelian–early Givetian.     

Age and tectonic setting of the Bavanat Cu–Zn–Ag Besshi-type volcanogenic massive sulfide deposit, southern Iran

The Bavanat Cu–Zn–Ag Besshi-type volcanogenic massive sulfide (VMS) deposit occurs within the Surian volcano-sedimentary complex in the Sanandaj–Sirjan zone (SSZ) of southern Iran. The Surian complex is comprised of pelite, sandstone, calcareous shale, basalt, gabbro sills, and thin-bedded limestone. Mineralization occurs as stratiform sheet-like and tabular orebodies hosted mainly by greenschist metamorphosed feldspathic and quartz feldspathic sandstone, basalt, and pelites. The basalts of the Surian complex show predominantly tholeiitic to transitional affinities, with a few samples that are alkalic in composition. Primitive mantle-normalized trace and rare earth element (REE) patterns of the Surian basalts display depletions in light REE, negative anomalies of Nb, Ta, and Ti, and positive anomalies of P. Positive P anomalies are indicative of minor crustal contamination. Furthermore, Th enrichments in the mid-ocean ridge basalt-normalized patterns of the Surian basalts are characteristic of rifted arc basalts emplaced in continental margin subduction zones. The high MgO content (>6?wt.%) of most Surian basalts and low TiO₂ content of two samples (0.53 and 0.62?wt.%) are characteristic of boninites. The aforementioned features of the basalts indicate arc tholeiites emplaced in intra-arc rift environments and continental margin subduction zones. U–Pb dating by laser ablation- inductively coupled plasma mass spectrometry of detrital zircons extracted from the host feldspathic and quartz feldspathic sandstone yields various ages that are predominantly Permian and Triassic; however, the youngest zircons give a mean Early Jurassic concordant U–Pb age of 191?±?12?Ma. This age, together with geological and petrochemical data, indicate that VMS mineralization formed in the Early Jurassic in pull-apart basins within the SSZ. These basins and the VMS mineralization may be temporally related to an intra-arc volcano–plutonic event associated with Neo-Tethyan oblique subduction.     

Geology,mineralogy, and sulfur isotope geochemistry of the Sargaz Cu–Zn volcanogenic massive sulfide deposit,Sanandaj–Sirjan Zone,Iran

The Sargaz Cu–Zn massive sulfide deposit is situated in the southeastern part of Kerman Province, in the southern Sanandaj–Sirjan Zone of Iran. The stratigraphic footwall of the Sargaz deposit is Upper Triassic to Lower Jurassic (?) pillowed basalt, whereas the stratigraphic hanging wall is andesite. Mafic volcanic rocks are overlain by andesitic volcaniclastics and volcanic breccias and locally by heterogeneous debris flows. Rhyodacitic flows and volcaniclastics overlie the sequence of basaltic and andesitic rocks. Based on the bimodal nature of volcanism, the regional geologic setting and petrochemistry of the volcanic rocks, we suggest massive sulfide mineralization in the Sargaz formed in a nascent ensialic back-arc basin. The current reserves (after ancient mining) of the Sargaz deposit are 3 Mt at 1.34% Cu, 0.38% Zn, 0.08%Pb, 0.24 g/t Au, and 7 g/t Ag. The structurally dismembered massive sulfide lens is zoned from a pyrite-rich base, to a pyrite?±?chalcopyrite-rich central part, and a sphalerite–chalcopyrite-rich upper part, with a sphalerite-rich zone lateral to the upper part. The main sulfide mineral is pyrite, with lesser chalcopyrite and sphalerite. The feeder zone, comprised of a vein stockwork consists of quartz–sulfide–sericite pesudobreccia and, in the deepest part, chlorite–quartz–pyrite pesudobreccia. Footwall hydrothermal alteration extends at least 70–80 m below the massive sulfide lens and more than a hundred meters along strike from the massive sulfide lens. Jasper and Fe–Mn bearing chert horizons lateral to the sulfide deposit represent low-temperature hydrothermal precipitates of the evolving hydrothermal system. Based on mineral textures and paragenetic relationships, the growth history of the Sargaz deposit is complex and includes: (1) early precipitation of sulfides (protore) on the seafloor as precipitation of fine-grained anhedral pyrite, sphalerite, quartz, and barite; (2) anhydrite precipitation in open spaces and mineral interstices within the sulfide mound followed by its subsequent dissolution, formation of breccia textures, and mound clasts and precipitation of coarse-grained pyrite, sphalerite, tetrahedrite–tennantite, galena and barite; (3) replacement of pre-existing sulfides by chalcopyrite precipitated at higher temperatures (zone refining); (4) continued “refining” led to the dissolution of stage 3 chalcopyrite and formation of a base-metal-depleted pyrite body in the lowermost part of the massive sulfide lens; (5) carbonate veins were emplaced into the sulfide lens, replacing stage 2 barite. The δ³⁴S composition of the sulfides ranges from +2.8‰ to +8.5‰ (average, +5.6‰) with a general increase of δ³⁴S ratios with depth within the massive sulfide lens and underlying stockwork zone. The heavier values indicate that some of the sulfur was derived from seawater sulfate that was ultimately thermochemically reduced in deep hydrothermal reaction zones.     

A combined fluid inclusion and S–Pb isotope study of the Neoproterozoic Pingshui volcanogenic massive sulfide Cu–Zn deposit,Southeast China

The Pingshui Cu–Zn deposit is located in the Jiangshan–Shaoxing fault zone, which marks the Neoproterozoic suture zone between the Yangtze block and Cathaysia block in South China. It contains 0.45 million tons of proven ore reserves with grades of 1.03 wt.% Cu and 1.83 wt.% Zn. This deposit is composed of stratiform, massive sulfide ore bodies, which contain more than 60 vol.% sulfide minerals. These ore bodies are hosted in altered mafic and felsic rocks (spilites and keratophyres) of the bimodal volcanic suite that makes up the Neoproterozoic Pingshui Formation. Metallic minerals include pyrite, chalcopyrite, sphalerite, tennantite, tetrahedrite and magnetite, with minor galena. Gangue minerals are quartz, sericite, chlorite, calcite, gypsum, barite and jasper. Three distinct mineralogical zones are recognized in these massive sulfide ore bodies: a distal zone composed of sphalerite + pyrite + barite (zone I); an intermediate zone characterized by a pyrite + sphalerite + chalcopyrite assemblages (zone II); and a proximal zone containing chalcopyrite + pyrite + magnetite (zone III). A thin, layer of exhalative jaspilite overlies the sulfide ore bodies except in the proximal zone. The volcanic rocks of the Pingshui Formation are all highly altered spilites and keratophyres, but their trace element geochemistry suggests that they were generated by partial melting of the depleted mantle in an island arc setting. Homogenization temperatures of the primary fluid inclusions in quartz from massive sulfide ores are between 217 and 328 °C, and their salinities range from 3.2 to 5.7 wt.% NaCl equivalent. Raman spectroscopy of the fluid inclusions showed that water is the dominant component, with no other volatile components. Fluid inclusion data suggest that the ore-forming fluids were derived from circulating seawater. The δ³⁴S values of pyrite from the massive sulfide ores range from − 3.6‰ to + 3.4‰, indicating that the sulfur was primarily leached from the arc volcanic rocks of the Pingshui Formation. Both pyrite from the massive sulfide ores and plagioclase from the spilites have similar lead isotope compositions, implying that the lead was also derived from the Pingshui Formation. The low lead contents of the massive sulfide ores and the geochemistry of their host rocks are similar to many VMS Cu–Zn deposits in Canada (e.g., Noranda) and thus can be classified as belonging to the bimodal-mafic subtype. The presence of magnetite and the absence of jaspilite and barite at the − 505 m level in the Pingshui deposit suggest that this level is most likely the central zone of the original lateral massive sulfide ore bodies. If this interpretation is correct, the deep part of the Pingshui Cu–Zn deposit may have significant exploration potential.     

Numerical heat and fluid flow modeling of the Hercynian Draa Sfar polymetallic (Zn–Pb–Cu) massive sulfide deposit,Central Jbilets,Morocco

Draa Sfar is a polymetallic (Zn–Pb–Cu) volcanogenic massive sulfide deposit with an actual resource of 13 Mt at 4.0% Zn and 1.3% Pb. It is part of the central Jbilets area known for its several Cu–Zn ore deposits. The ore is hosted in the upper Visean-Namurien sedimentary formation. Owing to the complexity of the geology of the ore deposits, numerical simulation approach was attempted to shed light into the temperature distribution, the circulation of the hydrothermal fluid and the genesis of massive sulfide ore bodies by evaluating the permeability, porosity, and thermal conductivity. On the basis of this simulation approach, the ore is predicted to be deposited at a temperature ranging between 230 and 290 °C. This temperature range is dependent on the pre-existing temperature of the discharge area where a metal-rich fluid precipitated the ore. The duration of the Draa Sfar ore body formation is predicted to be 15, 000 to 50, 000 years. Based on geological studies of Draa Sfar deposit together with the aforementioned results of the simulation approach, an ore genetic model for the massive sulfide ore bodies is proposed. In this model, the supply of ore-forming fluids is ensured by the combination of seawater and magmatic waters. Magma that generated rhyodacite dome acted as the heat source that remobilized the circulation of these ore-bearing fluids. The NW-SE trending faults acted as potential pathways for both the downward and upward migration of the ore-forming fluids. Due to their high permeability, the ignimbritic facies, host rocks of Draa Sfar ore bodies, have favored the circulation of the fluids. The mixing between the ore-forming fluids of magmatic origin and the descending seawaters and/or in situ pore waters led to the formation the ore bodies in 35,000 years. The position and size of the ore body, determined by the simulation approach, is consistent with the actual field geological data.     

Geology and genesis of the giant Beiya porphyry–skarn gold deposit,northwestern Yangtze Block,China

The Beiya ore deposit is located in the northwestern Yangtze Block, to the southeast of the Tibetan Plateau, SW China. The deposit is hosted by a porphyritic monzogranitic stock that is cross-cut by a porphyritic granite and later lamprophyre dikes. The whole-rock geochemistry of the porphyritic monzogranite and granite intrusions is both potassic and adakite-like, as evidenced by high K₂O/Na₂O (2.2 to 24.8), Sr/Y (53.2 to 143.2), and (La/Yb)_N (4.9 to 28.9) ratios. Both intrusions have comparable zircon U–Pb ages of ca. 36 Ma and εHf(t) values of − 6.8 to + 2.7. Zircons within these intrusions have Hf isotope crustal model ages with a prominent peak at ca. 840 Ma, and both of the intrusions have similar Sr–Nd–Pb isotopic compositions that are comparable to the compositions of amphibolite xenoliths hosted by potassic felsic intrusions in western Yunnan. The contemporaneous lamprophyre dikes show Nb–Ta depletion, enriched (⁸⁷Sr/⁸⁶Sr)_i and εNd(t), and extremely low Nb/U ratios (1.6–3.6), suggesting that these dikes were formed from magmas generated by partial melting of a metasomatized subcontinental lithospheric mantle (SCLM). The geochemistry of the porphyritic intrusions and the lamprophyre dikes suggests that the Beiya porphyries formed as a result of partial melting of a thickened and K-rich region of the lower crust, triggered by melting of metasomatized SCLM. The ca. 840 Ma U–Pb ages and εHf(t) values (− 6.8 to + 2.7) of xenocrystic zircons within the porphyritic intrusions suggest that these zircons were produced in a continental arc setting at ca. 840 Ma. The peak Hf model age of the zircons crystallized from the intrusions and the U–Pb ages of the xenocrystic zircons within the intrusions suggest that these porphyritic intrusions formed from magmas sourced from a juvenile crust that formed at ca. 840 Ma. This juvenile crust is most likely the source for the metals within the porphyry–skarn deposits in the study area, as the SCLM-derived lamprophyre dikes in this area are barren.Massive Fe–Au orebodies (~ 99 million metric tons at an average grade of 2.61 g/t Au) within the study area are generally located within the skarn-altered boundary of the porphyritic monzogranite stock and along the faults in the surrounding Triassic carbonates. The Fe–Au orebodies are spatially and genetically associated with skarn comprising garnet and diopside. Petrographic observations show that the massive Fe–Au orebodies mainly consist of hematite and magnetite with disseminated pyrite that hosts native gold and electrum.The porphyritic granite contains porphyry-style mineralization in the form of disseminated and veinlet-hosted pyrite and chalcopyrite. Pyrite-hosted lattice-bound gold is present within both the massive Fe–Au and the porphyry-type mineralization in the study area, and is present at concentrations up to 10 ppm Au (as determined by in situ LA-ICP-MS analysis). Subsequent weathering altered the primary magnetite–hematite–sulfide assemblage in the Fe–Au orebody into a magnetite–limonite assemblage, and generated laterite-type mineralization in which gold is hosted by limonite.     

Native bismuth,tsumoite, and Pb-bearing tsumoite from the Tarn’er copper-zinc massive sulfide deposit,northern Urals

Bismuth mineralization, including native bismuth, tsumoite (Bi_1.99–2.03Te_2.00), and Pb-bearing tsumoite (Bi_1.56–1.88Pb_0.45–0.14)_2.00–2.03Te_2.00, was identified in the Au-enriched disseminated ore at the Tarn’er massive sulfide deposit formed under the effect of a large diorite intrusion. Native bismuth associated with hessite forms idiomorphic inclusions in chalcopyrite. The assemblage of Pb-bearing tsumoite, hessite, and altaite occurs as angular allotriomorphic-granular inclusions in silicates or at the contact between silicate and sulfide aggregates. Tsumoite in allotriomorphic-granular aggregates with galena, hessite, and sphalerite is devoid of lead. Gold (Au_0.65Ag_0.35) was identified along with bismuth tellurides. The temperature of contact methamorphism (500–800°C) was estimated from the stability of andalusite, sillimanite, and cordierite. The morphology of the bismuth telluride aggregates in silicates and graphic intergrowth of tsumoite with galena suggest possible crystallization from anatectic melt. The positive correlation between Bi, Te, and Au confirms their probable joint transportation in the melt.     

Sequence of mineral formation in clastic ores of the Saf’yanovka volcanic-hosted copper massive sulfide deposit,the Central Urals

The bedded clastic ore widespread on the slopes and flanks of the deeply eroded sulfide mound at the Saf’yanovka volcanic-hosted copper massive sulfide deposit consists of products of destruction of the Paleozoic black smoker along with diverse newly formed sulfides. The size of ore clasts gradually decreases with distance from the massive ore mound, from more than tens of centimeters to a few millimeters. The clastic sediments are characterized by good preservation of sulfide material composed of hydrothermal sedimentary colloform pyrite, chalcopyrite with lamellae of relict isocubanite, and concentrically zoned sphalerite. Numerous pyrite framboids, nodules, and euhedral crystals; chalcopyrite segregations; and twinned sphalerite are typical of sulfide-bearing black shale. Enargite, tennantite, and galena were formed after pyrite, filling interstices between nodules or partially replacing and corroding the previously formed minerals. The interrelations between minerals show that the fine-clastic sulfide-bearing black shale underwent diagenesis in the presence of organic matter.     

The Boliden gold-rich volcanogenic massive sulfide deposit, Skellefte district, Sweden: new U–Pb age constraints and implications at deposit and district scale

The Boliden deposit (8.3 Mt at 15.9 g/t Au) is interpreted to have been formed between ca. 1894 and 1891 Ma, based on two new U–Pb ID-TIMS ages: a maximum age of 1893.9?+?2.0/?1.9 Ma obtained from an altered quartz and feldspar porphyritic rhyolite in the deposit footwall in the volcanic Skellefte group and a minimum age of 1890.8?±?1 Ma obtained from a felsic mass-flow deposit in the lowermost part of the volcano-sedimentary Vargfors group, which forms the stratigraphic hanging wall to the deposit. These ages are in agreement with the alteration and mineralization being formed at or near the sea floor in the volcanogenic massive sulfide environment. These two ages and the geologic relationships imply that: (1) volcanism and hydrothermal activity in the Skellefte group were initiated earlier than 1.89 Ga which was previously considered to be the onset of volcanism in the Skellefte group; (2) the volcano-sedimentary succession of the Vargfors group is perhaps as old as 1892 Ma in the eastern part of the Skellefte district; and (3) an early (synvolcanic) deformation event in the Skellefte group is evidenced by the unconformity between the ≤1893.9?+?2.0/?1.9 Ma Skellefte group upper volcanic rocks and the ≤1890.8?±?1 Ma Vargfors sedimentary and volcanic rocks in the Boliden domain. Differential block tilting, uplift, and subsidence controlled by synvolcanic faults in an extensional environment is likely, perhaps explaining some hybrid VMS-epithermal characteristics shown by the VMS deposits of the district.     

Mineralogy, geochemistry and stratigraphy of the Maslovsky Pt–Cu–Ni sulfide deposit, Noril’sk Region, Russia

We report new data on the stratigraphy, mineralogy and geochemistry of the rocks and ores of the Maslovsky Pt–Cu–Ni sulfide deposit which is thought to be the southwestern extension of the Noril’sk 1 intrusion. Variations in the Ta/Nb ratio of the gabbro-dolerites hosting the sulfide mineralization and the compositions of their pyroxene and olivine indicate that these rocks were produced by two discrete magmatic pulses, which gave rise to the Northern and Southern Maslovsky intrusions that together host the Maslovsky deposit. The Northern intrusion is located inside the Tungusska sandstones and basalt of the Ivakinsky Formation. The Southern intrusion cuts through all of the lower units of the Siberian Trap tuff-lavas, including the Lower Nadezhdinsky Formation; demonstrating that the ore-bearing intrusions of the Noril’sk Complex post-date that unit. Rocks in both intrusions have low TiO₂ and elevated MgO contents (average mean TiO₂ <1 and MgO?=?12?wt.%) that are more primitive than the lavas of the Upper Formations of the Siberian Traps which suggests that the ore-bearing intrusions result from a separate magmatic event. Unusually high concentrations of both HREE (Dy+Yb+Er+Lu) and Y (up to 1.2 and 2.1?ppm, respectively) occur in olivines (Fo_79.5 and 0.25% NiO) from picritic and taxitic gabbro-dolerites with disseminated sulfide mineralization. Thus accumulation of HREE, Y and Ni in the melts is correlated with the mineral potential of the intrusions. The TiO₂ concentration in pyroxene has a strong negative correlation with the Mg# of both host mineral and Mg# of host rock. Sulfides from the Northern Maslovsky intrusion are predominantly chalcopyrite–pyrrhotite–pentlandite with subordinate and minor amounts of cubanite, bornite and millerite and a diverse assemblage of rare precious metal minerals including native metals (Au, Ag and Pd), Sn–Pd–Pt–Bi–Pb compounds and Fe–Pt alloys. Sulfides from the Southern Maslovsky intrusion have δ ³⁴S?=?5–6‰ up to 10.8‰ in two samples whereas the country rock basalt have δ ³⁴S?=?3–4‰, implying there was no in situ assimilation of surrounding rocks by magmas.     

Deformation behavior of migmatites: insights from microstructural analysis of a garnet–sillimanite–mullite–quartz–feldspar-bearing anatectic migmatite at Rampura–Agucha,Aravalli–Delhi Fold Belt,NW India

International Journal of Earth Sciences - In the present study we investigate the microstructural development in mullite, quartz and garnet in an anatectic migmatite hosted within a Grenvillian-age...     

Facies architecture of the felsic lava‐dominated host sequence to the Thalanga massive sulfide deposit,Lower Ordovician,northern Queensland

The Thalanga volcanic‐hosted massive sulfide deposit occurs in the Cambro‐Ordovician Mt Windsor Subprovince in northern Queensland. The orebody comprises steeply dipping, stratiform, sheet‐like, polymetallic massive sulfide lenses. Overall, the volcanic facies architecture at Thalanga is dominated by quartz‐ and/or feldspar‐phyric lavas and synvolcanic intrusions that comprise coherent facies and in situ and resedimented autoclastic facies. Systematic phenocryst logging (mineralogy, abundance, size) has been used to discriminate separate emplacement units of rhyolite in the footwall and dacite in the hangingwall. Some of the petrographically different rhyolite and dacite types can also be distinguished using immobile‐element geochemistry. Rhyolitic lavas and intrusions in the footwall are weakly to strongly altered. Apparent clastic textures resulting from hydrothermal alteration and metamorphism are widely developed in the coherent facies. Genuine clastic textures are characterised by clasts with randomly oriented internal laminar or banded fabric (e.g. rotated, flow‐laminated clasts), marked and consistent differences in quartz phenocryst abundance and/or size range between clasts and matrix, and normal grading. Mass‐flow‐emplaced, rhyolitic breccia units delineate palaeo‐sea‐floor positions in the footwall that are potentially prospective for exhalative massive sulfide mineralisation. A comparison of the distribution of clastic and coherent facies with the geometry of strongly altered zones in the footwall indicates that intense hydrothermal fluid flow was independent of the facies arrangement. The massive sulfide lenses conformably overly altered footwall rhyolite and occur in a distinctive facies association which includes coarse quartz‐phenocryst‐rich rhyolitic sills with peperitic contacts and crystal‐rich polymictic breccia. The hangingwall to the orebody consists of largely unaltered dacitic lavas and synvolcanic intrusions and minor dacitic pumice breccia, dacitic breccia and polymictic volcanic breccia. The facies architecture shows that the Thalanga massive sulfide deposit formed in a below‐storm‐wave‐base depositional environment on top of an elevated, lava‐dominated, rhyolitic volcanic centre. A modern analogue for the setting of the Thalanga massive sulfide is the PACMANUS hydrothermal field on the crest of the dacite lava‐dominated Pual Ridge in the eastern Manus backarc basin (Papua New Guinea).     

U–Pb geochronology and Pb isotope characteristics of the Chahgaz volcanogenic massive sulphide deposit,southern Iran

The Chahgaz Zn–Pb–Cu volcanogenic massive sulphide (VMS) deposit occurs within a metamorphosed bimodal volcano–sedimentary sequence in the south Sanandaj–Sirjan Zone (SSZ) of southern Iran. This deposit is hosted by rhyodacitic volcaniclastics and is underlain and overlain by rhyodacitic flows, volcaniclastics, and pelites. Peperitic textures between rhyodacite flows and contact pelites indicate that emplacement of the rhyodacite occurred prior to the lithification of the pelites. The rhyodacitic flows are calc-alkaline, and show rare earth and trace elements features characteristic of arc magmatism. Zircons extracted from stratigraphic footwall and hanging-wall rhyodacitic flows of the Chahgaz deposit yield concordant U–Pb ages of 175.7 ± 1.7 and 172.9 ± 1.4 Ma, respectively, and a mean age of 174 ± 1.2 Ma. This time period is interpreted to represent the age of mineralization of the Chahgaz deposit. This Middle Jurassic age is suggested as a major time of VMS mineralization within pull-apart basins formed during Neo-Tethyan oblique subduction-related arc volcano-plutonism in the SSZ. Galena mineral separates from the layered massive sulphide have uniform lead isotope ratios of ²⁰⁶Pb/²⁰⁴Pb?=?18.604–18.617, ²⁰⁷Pb/²⁰⁴Pb?=?15.654–15.667, and ²⁰⁸Pb/²⁰⁴Pb?=?38.736–38.769; they show a model age of 200 Ma, consistent with the derivation of Pb from a Late Triassic, homogeneous upper crustal source.     

Petrography,mineral chemistry,fluid inclusion microthermometry and Re–Os geochronology of the Küre volcanogenic massive sulfide deposit (Central Pontides,Northern Turkey)

The Re–Os isotopic system is applied for the first time to the sulfide ores and the overlying black-shales at the Küre volcanogenic massive sulfide deposit of the Central Pontides, Northern Turkey. The ore samples collected include predominantly pyrite, accompanied by chalcopyrite, sphalerite and other species. Massive ore is almost free of gangues, whereas the stockwork ore includes quartz and calcite gangue. The composition of sphalerite is similar to ancient and modern massive sulfide mineralizations globally. Microthermometric studies from quartz from the stockwork ore has shown two populations of two-phase fluid inclusions with vapor/liquid ratios between 4 to 28%, low to intermediate T_h (161.5–317.0 °C) and low salinities (0.9–5 wt.% NaCl equiv.) which are mostly in good agreement with the ranges for volcanogenic massive sulfide mineralizations. These studies also suggest a H₂O–CaCl₂–KCl–MgCl₂ ore-forming fluid system in a shallower subsurface near the seafloor vents. The Re–Os dating of the LLHR sulfides yield a nominal depositional age of upper Toarcian for the massive sulfide mineralization. Two largely different model ages obtained are attributed to other pyrite crystallization events prior to and postdating the main sulfide deposition. Some lower homogenization temperatures (< 200 °C) from the quartz of the stockwork may also similarly be related to the post-VMS events. It is concluded that a submarine volcanic extrusion episode has continued until upper Toarcian in the Küre Basin, when it has entered a stagnation period that allowed the discharge of hydrothermally circulated sulfide-laden fluids from the seafloor vents. This age data promotes the palaeotectonic models interpreting the Küre Basin as a Permian–early Jurassic marginal back-arc basin of the Devonian-Triassic Karakaya Ocean. The Re–Os data from the overlying black-shale provide a glimpse to the initial Os isotope ratio of the water column at the time of the sedimentation (0.45–0.46 for 180 Ma). The lack of common Os from the sulfides does not let us to infer a source of Os and initial ¹⁸⁷Os/¹⁸⁸Os ratios from the black shale are not statistically robust to make a significant deduction. A further detailed study on the isotopic composition of the black shale strata may help us to make an apporach to the Os source(s) in the deposition environment of the Küre VMS deposit.     

Disseminated gold–sulfide mineralization at the Zhaima deposit,eastern Kazakhstan

The Zhaima gold–sulfide deposit is located in the northwestern part of the West Kalba gold belt in eastern Kazakhstan. The mineralization is hosted in Lower Carboniferous volcanic and carbonate rocks formed under conditions of marginal-sea and island-arc volcanic activity. The paper considers the mineralogy and geochemistry of primary gold–sulfide ore and Au-bearing weathering crusts. Au-bearing arsenopyrite–pyrite mineralization formed during only one productive stage. Disseminated, stringer–disseminated, and massive rocks are enriched in Ti, Cr, V, Cu, and Ni, which correspond to the mafic profile of basement. The main ores minerals are represented by finely acicular arsenopyrite containing Au (up to few tens of ppm) and cubic and pentagonal dodecahedral pyrite with sporadic submicroscopic inclusions of native gold. The sulfur isotopic composition of sulfides is close to that of the meteoritic standard (δ³⁴S =–0.2 to +0.2). The ⁴⁰Ar/³⁹Ar age of three sericite samples from ore veinlets corresponds to the Early Permian: 279 ± 3.3, 275.6 ± 2.9, and 272.2 ± 2.9 Ma. The mantle source of sulfur, ore geochemistry, and spatial compatibility of mineralization with basic dikes allow us to speak about the existence of deep fluid–magmatic systems apparently conjugate with the Tarim plume.     

Magnetite-rich calc-silicate alteration in relation to synvolcanic intrusion at the Ansil volcanogenic massive sulfide deposit, Rouyn–Noranda, Quebec, Canada

The Ansil Cu–Au volcanogenic massive sulfide deposit is located within an Archean-age cauldron infill sequence that contains the well-known Noranda base metal mining district. The deposit is unusual in that 17% of the massive pyrrhotite–chalcopyrite orebody is replaced by semi-massive to massive magnetite. Temporally associated with the magnetite formation are several calc-silicate mineral assemblages within the massive sulfide lens and the underlying sulfide stockwork vein system. Coarse-grained andradite–hedenbergite and ferroactinolite–ilvaite alteration facies formed in the immediate footwall to the massive magnetite–sulfide lens, whereas an epidote–albite–pyrite-rich mineral assemblage overprints the margins of the chlorite-rich stockwork zone. The epidote-rich facies is in turn overprinted by a retrograde chlorite–magnetite–calcite mineral assemblage, and the andradite–hedenbergite is overprinted first by ferroactinolite–ilvaite, followed by semi-massive to massive magnetite. The footwall sulfide- and magnetite-rich alteration facies are truncated by a late phase of the Flavrian synvolcanic tonalite–trondhjemite complex. Early phases of this intrusive complex are affected to varying degrees by calc-silicate-rich mineral assemblages that are commonly confined to miarolitic cavities, pipe vesicles and veins. The vein trends parallel the orientation of synvolcanic faults that controlled volcanism and hydrothermal fluid migration in the overlying cauldron succession. The magnetite-rich calc-silicate alteration facies are compositionally similar to those of volcanic-hosted Ca–Fe-rich skarn systems typical of oceanic arc terranes. Tonalite–trondhjemite phases of the Flavrian complex intruded to within 400 m of the base of the earlier-formed Ansil deposit. The low-Al trondhjemites generated relatively oxidized, acidic, Ca–Fe-rich magmatic–hydrothermal fluids either through interaction with convecting seawater, or by assimilation of previously altered rocks. These fluids migrated upsection along synvolcanic faults that controlled the formation of the original volcanogenic massive sulfide deposit. This is one of the few documented examples of intense metasomatism of a VMS orebody by magmatic–hydrothermal fluids exsolved from a relatively primitive composite sub-seafloor intrusion. Received: 15 April 1999 / Accepted: 20 January 2000     

Structural,lithological, and geochemical constraints on the dynamic magma plumbing system of the Jinchuan Ni–Cu sulfide deposit,NW China

Eastern and western portions of the Jinchuan ultramafic intrusion have previously been interpreted as dismembered segments of a single elongate intrusion by late faults. However, the different stratigraphic sequences of the two portions indicate that they are originally two separate intrusions, referred to as Eastern and Western intrusions in this study. The Eastern intrusion is characterized by a concentric distribution of rock types with a core of sulfide dunite enveloped by lherzolite, whereas the Western intrusion is composed of the Upper and Lower units, interpreted as magmatic mega cycles with regular variations in lithology and chemistry. In the Western intrusion, the Upper unit consists of fine-grained dunite, lherzolite, and pyroxenite from its base to its top. The MgO contents decrease upward from the dunites (42–45 wt.%) to the lherzolites (36–41 wt.%), while Al₂O₃ and incompatible elements increase upward. In contrast, the Lower unit consists of coarse-grained dunites and lherzolites containing 37–40 and 28–35 wt.% MgO, respectively. Sharp contacts between the Upper and Lower units and fine-grained dunite xenoliths at the top of the Lower unit indicate that the Lower unit intruded along the base of the Upper unit. Disseminated and net-textured sulfides primarily occur in the Lower unit and comprise the no. 24 ore body. Very low S contents (<100 ppm) of the wall rocks at Jinchuan indicate that they were not the source of S causing sulfide immiscibility. Sulfide segregation more likely occurred in deep-seated magma chambers, and sulfides were deposited in the Western intrusion when sulfide-bearing magmas passed through the intrusion. In contrast, the Eastern intrusion was formed by injections of sulfide-free and sulfide-bearing olivine-crystal mushes, respectively, from another deep-seated staging magma chamber. The Eastern and Western intrusions and the deep-seated magma chambers comprise a complicated magma plumbing system at Jinchuan. Normal faults played a significant role in the formation of the magma plumbing system and provided pathways for the magmas.     

A laser ablation ICP-MS study of platinum-group and chalcophile elements in base metal sulfide minerals of the Jinchuan Ni–Cu sulfide deposit,NW China

The paper presents concentrations of the platinum-group and chalcophile elements in the base metal sulfides (BMS) from the Jinchuan Ni–Cu sulfide deposit determined by laser ablation-inductively coupled plasma-mass spectrometry. Mass balance calculations reveal that pentlandite hosts a large proportion of Co, Ni and Pd (> 65%), and that pentlandite and pyrrhotite accommodate significant proportions of Re, Os, Ru, Rh, and Ag (~ 35–90%), whereas chalcopyrite contains a small amount of Ag (~ 10%) but negligible platinum-group elements. Iridium and Pt are not concentrated in the BMS and mostly occur in As-rich platinum-group minerals. The enrichments of Co, Ni, Re, Os, Ru, and Rh in pentlandite and pyrrhotite, and Cu in chalcopyrite are consistent with the fractionation of sulfide liquid and exsolution of pentlandite and pyrrhotite from the mono-sulfide solid solution (MSS). The Ir-bearing minerals exsolved from the MSS, depleting pentlandite and pyrrhotite in Ir, whereas sperrylite exsolved from the residual sulfide liquid on cooling. Diffusion of Pd from residual sulfide liquid into pentlandite during its exsolution from the MSS and crystallization of Pt-bearing minerals in the residual sulfide liquid resulted in the enrichment of Pd in pentlandite and decoupling between Pd and Pt in the Jinchuan net-textured and massive ores.     

Geological and isotopic constraints on the origin of the Anle carbonate-hosted Zn–Pb deposit in northwestern Yunnan Province,SW China

The Anle Zn–Pb deposit, hosted by Upper Cambrian dolostone, is located in the southern Songpan–Ganzi Block in southwest China. In this deposit, ore bodies occur as stratiform lenses and consist of galena, sphalerite and pyrite as ore minerals, and quartz, dolomite and calcite as gangue minerals. The mineralization shows mainly vein, banded and brecciated structures. Four ore bodies have been found in the Anle deposit, with a combined 2.0 million tonnes (Mt) of sulfide ores at average grades of 1.64 wt.% Pb, 6.64 wt.% Zn and 45 g/t Ag. Brown, brownish-yellow and yellow sphalerite samples have δ⁶⁶Zn values ranging from + 0.08 to + 0.10‰ (average + 0.09‰, n = 3), + 0.12 to + 0.38‰ (average + 0.24‰, n = 8) and + 0.40 to + 0.50‰ (average + 0.46‰, n = 3), respectively. We interpret the progressively heavier Zn isotopes from brown to yellow sphalerite as being led by kinetic Raleigh fractional crystallization. Calcite samples have δ¹³C_PDB and δ¹⁸O_SMOW values ranging from − 4.8 to − 0.2‰ (average − 1.7‰, n = 7) and + 17.9 to + 21.4‰ (average + 19.6‰, n = 7), respectively. Whole-rock δ¹³C_PDB and δ¹⁸O_SMOW values of the Cambrian ore-hosting dolostone range from + 0.1 to + 1.1‰ (average + 0.6‰, n = 3) and + 23.2 to + 24.1‰ (average + 23.6‰, n = 3), respectively. This suggests that carbon in the ore-forming fluids was provided by the host dolostone through carbonate dissolution. δ³⁴S_CDT values of sulfide samples range between − 1.3‰ and + 17.8‰ with an average value of + 6.3‰ (n = 25), lower than evaporites (such as barite + 19.8‰) in the overlaying Lower Ordovician sedimentary strata. The data suggest that sulfur in the hydrothermal fluids were derived from evaporites by thermo-chemical sulfate reduction (TSR). ²⁰⁶Pb/²⁰⁴Pb, ²⁰⁷Pb/²⁰⁴Pb and ²⁰⁸Pb/²⁰⁴Pb ratios for sulfide minerals range from 17.63 to 17.86, 15.58 to 15.69 and 37.62 to 37.95, respectively. The data are similar to those of the age-corrected Cambrian ore-hosting dolostone (²⁰⁶Pb/²⁰⁴Pb = 17.70–17.98, ²⁰⁷Pb/²⁰⁴Pb = 15.58–15.65 and ²⁰⁸Pb/²⁰⁴Pb = 37.67–38.06), but lower than those of age-corrected Ordovician sandstone and slate (²⁰⁶Pb/²⁰⁴Pb = 18.54–19.58, ²⁰⁷Pb/²⁰⁴Pb = 15.73–15.81 and ²⁰⁸Pb/²⁰⁴Pb = 38.44–39.60). This indicates that ore Pb was most likely to be derived from the Cambrian ore-hosting dolostone. Therefore, our new geological and isotopic evidence suggests that the Anle Zn–Pb deposit is best classified to be an epigenetic carbonate-hosted Mississippi Valley-type (MVT) deposit.