Structural geology of the Dugald River Zn---Pb---Ag deposit, Mount Isa Inlier, Australia

The sediment-hosted Zn---Pb---Ag deposit at Dugald River is situated 87 km northeast of Mount Isa, NW Queensland. It is a mid-scale base metal accumulation restricted to a black slate sequence of low metamorphic grade. The orebody is tabular and consists of fine- to medium-grained sulphides with a dominant mineralogy of sphalerite, pyrrhotite, pyrite, galena, quartz and muscovite. Three different ore types have been recognized based on mineralization textures; laminated, banded and brecciated. The present reserve stands at 38 million tons of ore averaging 13.0% Zn, 2.1% Pb and 42 g/t Ag. A structural investigation has revealed that six stages of deformation have affected the metasediments in the Dugald River area. The first four (D₁, D₂, D₃ and D₄) are characterized by the extensive development of folds and associated axial plane cleavage. They were all generated in a ductile regime and are of considerable significance for the structural evolution of this region as well as for the emplacement and localization of the sulphide mineralization. D₅ provides a transition towards brittle deformation developing strong kink folds with subhorizontal axial planes. D₆ was a brittle event, producing E-W-trending open folds and major NE and NW strike-slip faults crosscutting all the pre-existing structural elements plus segmenting the orebody. Correlation between the development of deformation and the formation of mineralization can be observed from macro- to microscales. Relationships of mineralization with folds and cleavage indicate a post-D₂ (dominant deformation event) and probably syn-D₄ deformation timing for the Zn---Pb---Ag mineralization at Dugald River, as suggested by the ubiquitous truncations of D₂ fabrics by ore mineral assemblages throughout the deposit.     

Structural geology of the Dugald River ZnPbAg deposit, Mount Isa Inlier, Australia

The sediment-hosted ZnPbAg deposit at Dugald River is situated 87 km northeast of Mount Isa, NW Queensland. It is a mid-scale base metal accumulation restricted to a black slate sequence of low metamorphic grade. The orebody is tabular and consists of fine- to medium-grained sulphides with a dominant mineralogy of sphalerite, pyrrhotite, pyrite, galena, quartz and muscovite. Three different ore types have been recognized based on mineralization textures; laminated, banded and brecciated. The present reserve stands at 38 million tons of ore averaging 13.0% Zn, 2.1% Pb and 42 g/t Ag. A structural investigation has revealed that six stages of deformation have affected the metasediments in the Dugald River area. The first four (D₁, D₂, D₃ and D₄) are characterized by the extensive development of folds and associated axial plane cleavage. They were all generated in a ductile regime and are of considerable significance for the structural evolution of this region as well as for the emplacement and localization of the sulphide mineralization. D₅ provides a transition towards brittle deformation developing strong kink folds with subhorizontal axial planes. D₆ was a brittle event, producing E-W-trending open folds and major NE and NW strike-slip faults crosscutting all the pre-existing structural elements plus segmenting the orebody. Correlation between the development of deformation and the formation of mineralization can be observed from macro- to microscales. Relationships of mineralization with folds and cleavage indicate a post-D₂ (dominant deformation event) and probably syn-D₄ deformation timing for the ZnPbAg mineralization at Dugald River, as suggested by the ubiquitous truncations of D₂ fabrics by ore mineral assemblages throughout the deposit.     

Draa Sfar, Morocco: A Visean (331 Ma) pyrrhotite-rich, polymetallic volcanogenic massive sulphide deposit in a Hercynian sediment-dominant terrane

Draa Sfar is a Visean, stratabound, volcanogenic massive sulphide ore deposit hosted by a Hercynian carbonaceous, black shale-rich succession of the Jebilet terrane, Morocco. The ore deposit contains 10 Mt grading 5.3 wt.% Zn, 2 wt.% Pb, and 0.3 wt.% Cu within two main massive sulphides orebodies, Tazakourt (Zn-rich) and Sidi M'Barek (Zn–Cu rich). Pyrrhotite is by far the dominant sulphide (70 to 95% of total sulphides), sphalerite is fairly abundant, chalcopyrite and galena are accessory, pyrite, arsenopyrite and bismuth minerals are rare. Pyrrhotite is monoclinic and mineralogical criteria indicate that it is of primary origin and not formed during metamorphism. Its composition is very homogeneous, close to Fe₇S₈, and its absolute magnetic susceptibility is 2.10^− 3 SI/g. Ar–Ar dating of hydrothermal sericites from a coherent rhyolite flow or dome within the immediate deposit footwall indicates an age of 331.7 ± 7.9 Ma for the Draa Sfar deposit and rhyolite volcanism.The Draa Sfar deposit has undergone a low-grade regional metamorphic event that caused pervasive recrystallization, followed by a ductile–brittle deformation event that has locally imparted a mylonitic texture to the sulphides and, in part, is responsible for the elongated and sheet-like morphology of the sulphide orebodies. Lead isotope data fall into two compositional end-members. The least radiogenic end-member, (²⁰⁶Pb/²⁰⁴Pb = 18.28), is characteristic of the Tazakourt orebody, whereas the more radiogenic end-member (²⁰⁶Pb/²⁰⁴Pb  18.80) is associated with the Sidi M'Barek orebody, giving a mixing trend between the two end-members. Lead isotope compositions at Draa Sfar testify to a significant continental crust source for the base metals, but are different than those of the Hajar and South Iberian Pyrite Belt VMS deposits.The abundance of pyrrhotite versus pyrite in the orebodies is attributed to low fO₂ conditions and neither a high temperature nor a low aH₂S (below 10^− 3) is required. The highly anoxic conditions required to stabilize pyrrhotite over pyrite are consistent with formation of the deposit within a restricted, sediment-starved, anoxic basin characterized by the deposition of carbonaceous, pelagic sediments along the flank of a rhyolitic flow-dome complex that was buried by pelitic sediments. Deposition of sulphides likely occurred at and below the seafloor within anoxic and carbonaceous muds.Draa Sfar and other Moroccan volcanogenic massive sulphide deposits occur in an epicontinental volcanic domain within the outer zone of the Hercynian belt and formed within a sedimentary environment that has a high pelagic component. In spite of the diachronous emplacement between the IPB deposits (late Devonian to Visean) and Moroccan deposits (Dinantian), all were formed around 340 ± 10 Ma following a major phase of the Devonian compression.     

安徽铜陵冬瓜山铜矿床的叠加改造成矿机制：来自矿石结构的证据

长江中、下游地区块状硫化物矿床普遍受到燕山期岩浆及其热液的改造与叠加.本文以铜陵冬瓜山矿床为例,探讨这类矿床的成矿机制.该矿床主要由层状硫化物矿体组成,伴有矽卡岩型和斑岩型矿体.野外地质观察及室内矿相学的研究表明,冬瓜山层状矿体中矿石遭受了强烈的热变质作用及热液交代作用.进变质过程中形成的结构主要为黄铁矿受燕山期岩浆侵...     

Application of the sphalerite geobarometer to some skarn-type ore deposits

Based on the equation recently determined, formation pressures of skarn-type ore deposits were estimated from the composition of sphalerite coexisting with pyrite and hexagonal pyrrhotite. As criteria for equilibrium among sphalerite, pyrite and hexagonal pyrrhotite, the following three points were carefully checked on each specimen: 1) the presence of hexagonal pyrrhotite, 2) no time sequences among the formation of sulfide minerals, and 3) no compositional variation in sphalerite. Most of the Cu-Fe skarn deposits studied were formed under pressures of more than 1 kb, whereas Zn-Pb(-Cu-Fe) deposits tend to have formed at relatively shallow environments, namely under less than 1 kb. The calculated pressures are qualitatively consistent with the depth of formation of deposits estimated from the geological evidences. The sphalerite geobarometry is quite sensitive even at low pressure ranges, and it is applicable to the deposits formed under shallow conditions.     

High-pressure metamorphism of stratiform sulphide deposits from the Diahot region,New Caledonia

Stratiform Cu-Pb-Zn (-Au-Ag) mineralization associated with black carbonaceous schists and acid metatuffs is restricted to distinct horizons within the Cretaceous sequence of the Diahot region. The sulphides occur in sharply bounded lenses which show varying degrees of compositional banding conformable with the foliation of the country schists. The deposits are sedimentary-exhalative of the Rio Tinto-type and have been modified by mid-Tertiary high-pressure metamorphism (lawsonite-albite and glaucophanitic greenschist facies). The ores are not strongly deformed by the metamorphism and sedimentary structures, pyrite framboids and atoll structures are preserved in some deposits. With increasing metamorphic grade sphalerite becomes more iron-rich, pyrrhotite becomes more abundant, and the sulphides show a general increase in grain-size which parallels that of the silicates in the enclosing rocks. In the more highly metamorphosed deposits the sulphide associations are retrograde assemblages. There is no evidence of large-scale metamorphic remobilization of sulphides. No differences were observed in either the sulphide assemblages or in the composition of the sulphides to indicate that the metamorphism was of the high pressure rather than the low pressure type.     

Stromeyerite and mckinstryite from the Godejord polymetallic sulphide deposit,central Norweigan Caledonides

The Cu-Ag-S minerals, stromeyerite and mckinstryite, have been found for the first time in a stratabound polymetallic pyritic deposit in the Caledonides of central Norway. The surface specimens examined contained approximately 0.5% Ag, 1.8% Cu, 15.0% Zn and over 10 g/t Au and showed the mineral association pyrite, sphalerite, chalcopyrite, galena, tennantite, bornite, Cu-Ag sulphides, covelline, native Au, a Cu-Sn sulphide, and a new mineral of composition Ag₅CuTeS₂. The Cu-Ag sulphides appear to be replacing preexisting sulphides, with the exception of pyrite and sphalerite. The nature of this replacement is discussed. Analyses, by microprobe, of the Cu-Ag-S phases are reported and compared with published data. The stromeyerite shows an average composition Cu_1.01Ag S, the mckinstryite Cu_0.77Ag_1.19S. Values are reported of the reflectance at 542 nm for both minerals. The data indicate that stromeyerite is optically positive with Rg: 30.7%, Rm: 27.3%, Rp: 25.8% while mckinstryite is negative with Rg: 32.5%, Rm: 31.9%, Rp: 27.6%.     

The adsorption of gold(I) hydrosulphide complexes by iron sulphide surfaces

The adsorption of gold by pyrite, pyrrhotite, and mackinawite from solutions containing up to 40 mg/kg (8 μm) gold as hydrosulphidogold(I) complexes has been measured over the pH range from 2 to 10 at 25°C and at 0.10 m ionic strength (NaCl, NaClO₄). The pH of point of zero charge, pH_pzc, has been determined potentiometrically for all three iron sulphides and shown to be 2.4, 2.7, and 2.9 for pyrite, pyrrhotite, and mackinawite, respectively. In solutions containing hydrogen sulphide, the pH_pzc is reduced to values below 2. The surface charge for each sulphide is therefore negative over the pH range studied in the adsorption experiments. Adsorption was from 100% in acid solutions having pH < 5.5 (pyrite) and pH < 4 (mackinawite and pyrrhotite). At alkaline pH’s (e.g., pH = 9), the pyrite surface adsorbed 30% of the gold from solution, whereas the pyrrhotite and mackinawite surfaces did not adsorb.The main gold complex adsorbed is AuHS°, as may be deduced from the gold speciation in solution in combination with the surface charge. The adsorption of the negatively charged Au(HS)₂⁻ onto the negatively charged sulphide surfaces is not favoured. The X-ray photoelectron spectroscopic data revealed different surface reactions for pyrite and mackinawite surfaces. While no change in redox state of adsorbent and adsorbate was observed on pyrite, a chemisorption reaction has been determined on mackinawite leading to the reduction of the gold(I) solution complex to gold(0) and to the formation of surface polysulphides. The data indicate that the adsorption of gold complexes onto iron sulphide surfaces such as that of pyrite is an important process in the “deposition” of gold from aqueous solutions over a wide range of temperatures and pressures.     

Petrography, mineralogy and geochemistry of the Zarshuran Carlin-like gold deposit, northwest Iran

Gold mineralisation at Zarshuran, northwestern Iran, is hosted by Precambrian carbonate and black shale formations which have been intruded by a weakly mineralised granitoid. Granitoid intrusion fractured the sedimentary rocks, thereby improving conditions for hydrothermal alteration and mineralisation. Silicification is the principal hydrothermal alteration along with decalcification and argillisation. Three hydrothermal sulphide mineral assemblages have been identified: an early assemblage of pyrrhotite, pyrite and chalcopyrite; then widespread base metal sulphides, lead-sulphosalts and zoned euhedral arsenical pyrite; and finally late network arsenical pyrite, massive and colloform arsenical pyrite, colloform sphalerite, coloradoite, and arsenic–antimony–mercury–thallium-bearing sulphides including orpiment, realgar, stibnite, getchellite, cinnabar, lorandite and a Tl-mineral, probably christite. Most of the gold at Zarshuran is detectable only by quantitative electron microprobe and bulk chemical analyses. Gold occurs mainly in arsenical pyrite and colloform sphalerite as solid solution or as nanometre-sized native gold. Metallic gold is found rarely in hydrothermal quartz and orpiment. Pure microcrystalline orpiment, carbon-rich shale, silicified shale with visible pyrite grains and arsenic minerals contain the highest concentrations of gold. In many ways Zarshuran appears to be similar to the classic Carlin-type sediment-hosted disseminated gold deposits. However, relatively high concentrations of tellurium at Zarshuran, evidenced by the occurrence of coloradoite (HgTe), imply a greater magmatic contribution in the mineralising hydrothermal solutions than is typical of Carlin-type gold deposits. Received: 13 May 1999 / Accepted: 2 February 2000     

The Bepkong gold deposit,Northwestern Ghana

The Bepkong gold deposit is located in the Wa–Lawra belt of the Paleoproterozoic Baoulé-Mossi domain of the West African Craton, in NW Ghana. It occurs in pelitic and volcano-sedimentary rocks, metamorphosed to greenschist facies, in genetic association with zones of shear interpreted to form during the regional D₃ deformational event, denominated D_B1 at the deposit scale. The ore zone forms a corridor-like body composed of multiple quartz ± carbonate veins surrounded by an alteration envelope, characterized by the presence of chlorite, calcite, sericite, quartz and disseminated pyrite, arsenopyrite plus subordinate pyrrhotite and chalcopyrite. The veins contain only small proportions of pyrite, whereas most of the sulphides, particularly arsenopyrite, occur in the altered host rock, next to the veins. Pyrite is also common outside of the ore zone. Gold is found in arsenopyrite, where it occurs as invisible gold and as visible – albeit micron-size – grains in its rims, and as free gold within fractures cross-cutting this sulphide. More rarely, free gold also occurs in the veins, in fractured quartz. In the ore zone, pyrite forms euhedral crystals surrounding arsenopyrite, but does not contain gold, suggesting that it formed at a late stage, from a gold-free hydrothermal fluid.     

Geochemical alteration halos around the Mount Morgan gold-copper deposit, Queensland, Australia

The Mount Morgan Au-Cu pyritic massive sulphide deposit occurs in a north-trending belt of Middle Paleozoic volcanic rocks located in south-central Queensland. The host rocks for the deposit are a normal sequence of rhyolitic tuff that have a north-northwest regional strike and easterly dips of 20° to 30°. The tuff contains thin units of chert, jasperoid and carbonate.The Mount Morgan deposit was represented by a zone of sulphide mineralization 600 m long, 100–200 m wide and 300 m deep that transects stratigraphy and can be divided into: (1) an oxidized zone, characterized by a hematitic, Au-enriched gossan with minor stratiform sphalerite-argillite; and (2) a primary zone which can be subdivided into an upper zone of greater than 50% sulphide minerals (Main Pipe orebody), and a lower siliceous stockwork zone with approximately 20% sulphide minerals (Sugarloaf orebody). Pyrite is the most abundant sulphide mineral in both the upper and lower primary zones with lesser pyrrhotite and accessory chalcopyrite, sphalerite and gold. A zone of silicification forms an envelope around the orebody and extends stratigraphically downwards in a pipe-like zone for greater than 750 m. The orebody contained 67 Mt of 4.87 g/t Au and 0.70% Cu.The distribution and variation of between 7 and 29 elements and specific conductance were examined in 1252 samples of the host rocks taken from diamond drill core and surface outcrop. The host rocks in the immediate vicinity of the deposit are marked by the development of three distinct but overlapping chemical and mineralogical zones representing an outward progression from the most intensive to a less intensive alteration. A 50-m-thick siliceous inner zone of intensely altered rocks, depleted in all investigated elements except Si, surrounds the orebody. This zone passes outward into a 100-m-thick middle zone of dominantly sericite-pyrite characterized by high concentrations of K, Fe, Cu and Co. The sericite-pyrite zone, in turn, passes into an outer 100-m-thick chlorite zone with high Fe, Mg, Mn and Zn concentrations. High concentrations of H₂O⁺ are associated with the sericite-pyrite zone and the chlorite zone. The alteration pipe underlying the Mount Morgan orebody is characterized by depletions in Na, Ca and K and enrichments in Fe and Mg. A non-economic pyrite body contained within the alteration pipe has spatially restricted enrichment halos of Fe, Mg, Zn, Cu and Co.     

Gold-bearing hedenbergite skarns from the SW contact of the Andorra granite (Central Pyrenees, Spain)

Several varieties of skarn outcrop have been found to develop along the contact between the Andorra granite and the Devonian limestones. The skarns contain variable amounts of gold ranging up to 5 g/t, always associated with sulphides. The sulphides in the skarn include arsenopyrite and pyrrhotite with lesser amounts of chalcopyrite, galena, sphalerite and Bi-minerals. Geothermometric and geobarometric data indicate the skarns formed at about 2 kbar and temperatures ranging from 500 ° to 350 °C from CO₂-free polysaline brines at a slightly acidic pH and oxygen fugacity which decreases with time from the pyrite-pyrrhotite-magnetite towards the QFM buffer. Available data on gold solubility suggest that sufficient quantities of gold to form an ore deposit could have been transported as AuCl ₂ ^- at the high temperatures and salinities under which the skarns formed. Both gold deposition and sulphide precipitation could have occurred due to a decrease in temperature and/or oxygen fugacity.     

Lewis Ponds, a hybrid carbonate and volcanic-hosted polymetallic massive sulphide deposit, New South Wales, Australia

The Lewis Ponds Zn–Pb–Cu–Ag–Au deposit, located in the eastern Lachlan Fold Belt, central western New South Wales, exhibits the characteristics of both volcanic-hosted massive sulphide and carbonate-hosted replacement deposits. Two stratabound massive to disseminated sulphide zones, Main and Toms, occur in a tightly folded Upper Silurian sequence of marine felsic volcanic and sedimentary rocks. They have a combined indicated resource of 5.7 Mt grading 3.5% Zn, 2.0% Pb, 0.19% Cu, 97 g/t Ag and 1.9 g/t Au. Main Zone is hosted by a thick unit of poorly sorted mixed provenance breccia, limestone-clast breccia and quartz crystal-rich sandstone, whereas Toms Zone occurs in the overlying siltstone. Pretectonic carbonate–chalcopyrite–pyrite and quartz–pyrite stringer veins occur in the footwall porphyritic dacite, south of Toms Zone. Strongly sheared dolomite–chalcopyrite–pyrrhotite veins directly underlie the Toms massive sulphide lens. The mineralized zones consist predominantly of pyrite, sphalerite and galena. Paragenetically early framboidal, dendritic and botryoidal pyrite aggregates and tabular pyrrhotite pseudomorphs of sulphate occur throughout the breccia and sandstone beds that host Main Zone, but are rarely preserved in the annealed massive sulphide in Toms Zone. Main and Toms zones are associated with a semi-conformable hydrothermal alteration envelope, characterized by texturally destructive chlorite-, dolomite- and quartz-rich assemblages. Dolomite, chlorite, quartz, calcite and sulphides have selectively replaced breccia and sandstone beds in the Main Zone host sequence, whereas the underlying porphyritic dacite is weakly sericite altered. Vuggy and botryoidal textures resulted from partial dissolution of the dolomite-altered sedimentary rocks and unimpeded growth of base metal sulphides, carbonate and quartz into open cavities. The intense chlorite-rich alteration assemblage, underlying Toms Zone, grades outward into a weak pervasive sericite–quartz assemblage with distance from the massive sulphide lens. Limestone clasts and hydrothermal dolomite at Lewis Ponds are enriched in light carbon and oxygen isotopes. The dolomite yielded ¹³C_VPDB values of –11 to +1 and ¹⁸O_VSMOW values of 6 to 16. Liquid–vapour fluid inclusions in the dolomite have low salinities (1.4–7.7 equiv. wt% NaCl) and homogenization temperatures (166–232°C for 1,000 m water depth). Dolomitization probably involved fluid mixing or fluid–rock interactions between evolved heated seawater and the limestone-bearing facies, prior to and during mineralization. ³⁴S_VCDT values range from 2.0 to 5.0 in the massive sulphide and 3.9 to 7.4 in the footwall carbonate–chalcopyrite–pyrite stringer veins, indicating that the hydrothermal fluid may have contained mamgatic sulphur and a component of partially reduced seawater. The sulphide mineral assemblages at Lewis Ponds are consistent with moderate to strongly reduced conditions during diagenesis and mineralization. Low temperature dolomitization of limestone-bearing facies in the Main Zone host sequence created secondary porosity and provided a reactive host for fluid-rock interactions. Main Zone formed by lateral fluid flow and sub-seafloor replacement of the poorly sorted breccia and sandstone beds. Base metal sulphide deposition probably resulted from dissolution of dolomite, fluid mixing and increased fluid pH. Pyrite, sphalerite and galena precipitated from a relatively low temperature, 150–250°C hydrothermal fluid. In contrast, Toms Zone was emplaced into fine-grained sediment at or near the seafloor, above a zone of focused up-flowing hydrothermal fluids. Copper-rich assemblages were deposited in the Toms Zone footwall and massive sulphide lenses in Main and Toms zones as the hydrothermal system intensified. During the D₁ deformation, fracture-controlled fluids within the Lewis Ponds fault zone and adjacent footwall volcanic succession remobilized sulphides into syntectonic quartz veins. Lewis Ponds is a rare example of a synvolcanic sub-seafloor hydrothermal system developed within fossiliferous limestone-bearing facies. The close spatial association between limestone, hydrothermal dolomite, massive sulphide and dacite provides a basis for new exploration targets elsewhere in New South Wales.Editorial handling: D. Lentz     

Hydrothermal deposition on the East Pacific rise at 21°N

In the spring of 1979, 350°C springs precipitating hydrothermal sulphides and sulphates directly on to the sea-floor were discovered on the crest of the East Pacific Rise (EPR) at 21°N by the astonished scientific party of the RISE submersible expedition. These hot springs are within a linear field of active and inactive hydrothermal vents extending 6 km along the rise axis. Typically the mineral deposits at EPR, 21°N consist of basal sulphide mounds surmounted by mineralized sulphide-sulphate edifices, or “chimneys”, reaching heights up to 13 m above the sea floor. The mounds rest directly on fresh basalt and cover areas up to 450 m². Chimneys atop mounds may be active or dead. The hottest active chimneys (350°C) spew forth fluids blackened by fine-grained sulphide precipitates, dominantly hexagonal pyrrhotite and iron-rich sphalerite. These “black smokers” are distinguished from cooler “white smoker” chimneys which are encrusted by worm tubes and emit milky fluids bearing amorphous silica, barite, and pyrite.     

Sulphur‐isotope study of the massive sulphide orebody at Woodlawn,New South Wales

³⁴S/³²S ratios have been measured in a suite of samples from the stratabound, volcanogenic massive sulphide deposit at Woodlawn, N.S.W. ³⁴S values for the sulphides vary as follows: in the ore horizon, pyrite +6.7 to +9.2%. (mean +8.1‰), sphalerite +5.2 to +8.6‰. (mean +6.9‰), chalcopyrite +6.4 to +7.0‰ (mean +6.7‰) and galena +2.8 to +5.5‰ (mean +4.4‰); in the vein mineralization, the host volcanics—pyrite +8.7 to +11.4%. (mean +9.8‰), sphalerite +7.8 to + 10.3‰ (mean +9.2‰), chalcopyrite; +8.8 to +10.1‰ (mean +9.2‰) and galena +6.9 to +7.2‰ (mean +7.1‰). Barite from the upper ore horizon levels has an isotopic composition of +30.0‰, consistent with its having originated from Silurian ocean sulphate. The general order of ³⁴S enrichment in the sulphides is pyrite > chalcopyrite ～ sphalerite > galena. Isotopic fractionations in the systems galena/sphalerite/pyrite and chalcopyrite/pyrite indicate an equilibration temperature of 275–300°C. This temperature is considered to represent that of sulphide deposition.     

Tsumoite (BiTe) and associated Ni-PGE mineralization from Gondpipri mafic-ultramafic complex,Bastar Craton,Central India: mineralogy and genetic significance

This paper reports the occurrence of Tsumoite (a bismuth telluride) in the Heti Cu-Ni-PGM prospect, Gondpipri mafic-ultramafic complex, Central India. The Gondpipri complex consists of several tectonically dismembered gabbronorite-gabbro-anorthositic gabbro — olivine gabbro -websterite disposed in ～10 km long tonalite-trondhjemitegranodiorite (TTG) and charnockite-enderbite suite of rocks. The mineralization occurs in the sulphide zone hosted by gabbro variants. The host rocks have been deformed and metamorphosed to granulite grade and subjected to various degrees of hydrothermal alteration. The mineralization comprises chalcopyrite, pentlandite, pyrrhotite, cubanite, millerite, and pyrite. In addition to these, occur (1) tsumoite (2) PGM in the form of moncheite, merenskyite, Pd-mellonite, and Pt-Pd-Te-Bi-Fe-S alloy. The present study indicates that the mineralization occurs in two stages related to: (i) magmatic and (ii) hydrothermal remobilization and transport of Cu-rich sulphides, tsumoite and PGM, and their re-deposition in hydrosilicate alteration zones. It is possible that the mineralization at Heti formed at different stages of bismuth activity under variable fS₂, T, and fTe₂ conditions due to change in total concentration of Te and S and /or cooling. Since the role of S is limited, Te and cooling are important factor influencing mineralogy and composition of tsumoite and associated mineralization. Mineralization occurs in two different modes of occurrences. The early mineralisation occur as blebs, specks and dissemination of sulphides, viz. pyrrhotite, chalcopyrite, pentlandite and minor pyrite ± PGM, whereas later mineralisation occur as stringers, minor veins of sulphides viz. pyrite, millerite, cubanite, sijenite, tsumoite and ± PGM. Mineral assemblages and textural relationships at Heti has indicated precipitation of tsumoite and associated PGM along fractures and secondary silicates, which confirms their hydrothermal origin.     

Ore mineralogy and sulfur isotope study of the massive sulfide deposit of Filon Norte,Tharsis Mine,Spain

The volcanogenic massive sulfide deposit of Filon Norte at Tharsis is hosted by carbonaceous black slate and connected only partly with stockwork veins. The massive ores are usually composed of fine-grained pyrite with subordinate amounts of sphalerite, chalcopyrite, galena and arsenopyrite. Monoclinic pyrrhotite sometimes occurs in massive pyritic ores in the apparently middle and upper horizons of the orebody, and siderite-rich ores are interstratified with compact pyritic ores in the apparently lower horizons. From the occurrence of monoclinic pyrrhotite, together with the FeS contents of sphalerite mostly ranging from 11 to 16 mol %, it is inferred that the sulfide minerals of the massive orebody were precipitated in euxinic muds on the sea-floor at temperatures below 250°C. The negatively shifted, highly variable ³⁴S values of the massive ores and their close similarity to those of the underlying black slates strongly suggest that the sulfide sulfur of the massive orebody and the slates is cognate and biogenic.     

Multiphase evolution in the black-shale-hosted Ni–Cu–Zn–Co deposit at Talvivaara,Finland

The Talvivaara deposit contains 1550 Mt of ore averaging 0.22% Ni, 0.13% Cu, 0.49% Zn and 0.02% Co. The precursors of the host rocks were deposited 2.1–1.9 Ga ago in a stratified marine basin. Fractured talc-carbonate rocks delineate the eastern border of the deposit and serpentinites and talc-carbonate rocks occur along the rift-related sequence to the north and south of Talvivaara. Characteristic features are high concentrations of organic carbon and sulphur with median values of 7.6% and 8.2%, respectively. Organic carbon is graphitic at present and a variety of sulphide textures occur, representing multiphase evolution during diagenesis, tectonic deformation and medium-grade regional metamorphism. The main sulphides of the Talvivaara ore are pyrrhotite, pyrite, sphalerite, chalcopyrite and pentlandite. Sulphides occur both as fine-grained disseminations and coarse grains or aggregates. Chalcopyrite mainly occurs in joint surfaces and quartz-sulphide veins and pentlandite occur as inclusions in pyrrhotite. Alabandite (MnS) occurs in black shales and black metacarbonate rocks. The early low-T sulphide minerals were overprinted by later stage processes. No framboidal pyrite is any longer present, but spheroidal pyrite with a grain size of < 0.01 mm and containing up to 0.7% Ni occurs. During the deposition of the organic-rich mud the anoxic/euxinic bottom waters were enriched in Ni⁺, Cu⁺ and Zn^2 +. Sulphur isotope δ³⁴S values indicate mixing of sulphur derived from different processes or fractionation by sulphate reduction in a restricted basin. Both thermochemical and bacterial sulphate reductions were important for the generation of reduced sulphur.     

Polymetamorphism of ores in Precambrian stratiform massive sulfide deposits at Ambaji-Deri,Western India

Massive stratiform zinc-lead-copper sulfide ores, in association with cordierite-anthophyllite rocks, occur in adjacent localities of Ambaji and Deri, in Western India. The metasedimentary country rocks, interlayered with amphibolites and intruded by acidic to intermediate plutonic rocks, belong to the Precambrian Delhi Supergroup. The ore minerals identified by detailed mineragraphic studies include: sphalerite, galena, chalcopyrite, pyrite, pyrrhotite (both monclinic and hexagonal phases), magnetite, ilmenite, rutile, arsenopyrite, molybdenite, cubanite, mackinawite, boulangerite, gudmundite, meneghinite, lautite, tenantite, native bismuth, native silver, chalcocite and covellite. The common sulfide-silicate schistosity in the ores, flowage of sulfide streaks and tails around rotated poikiloblasts and in their pressure shadow region developed during early folding (F₁) and regional metamorphism of the rocks under green schist facies condition. These were superimposed by a pervasive hornfelsic fabric involving sulfides and silicates and including microfabrics due to annealing and grain growth in sulfides, during a subsequent phase of low pressure thermal metamorphism and related tectonism (F₂). Finally certain deformation features and some uncommon fabrics like martensitic lamellae in galena and subgrains in sphalerite developed during a mild deformation episode (F₃) in the waning stages of tectonism in the area. Compositional change in the ores during thermal metamorphism was minimal.