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1.
The Tyndrum Pb+Zn veins, hosted by late Proterozoic quartzites, were probably generated in the Tournaisian (360 Ma). By determination of sulphur isotopic ratios of vein minerals three aspects of the Tyndrum mineralization were addressed, (i) sulphate sulphur sources; (ii) reduced sulphur source; (iii) isotopic equilibrium in the vein system including geothermometry. Twelve galenas have δ34S values ranging from +3.55 ‰ to +6.38 ‰ (this excludes one value of +11.21 ‰ from a large but nearly barren quartz vein). Other sulphides are enriched or depleted in 34S in the sense expected for isotopic equilibrium although there is no evidence for isotopic equilibrium between the vein minerals. The sulphide sulphur source was probably in the Dalradian metasediments where disseminated pyrite averages +6 ‰. Baryte had δ34S values averaging 14 ‰ and was therefore not in isotopic equilibrium with sulphides: a continental groundwater source is most likely.  相似文献   

2.
The Lumwana Cu (± Co ± U) deposits of NW Zambia are large, tabular, disseminated ore bodies, hosted within the Mwombezhi Dome of the Lufilian Arc. The host rocks to the Lumwana deposits are two mineralogically similar but texturally distinct gneisses, a granitic to pegmatitic gneiss and a banded to augen gneiss which both comprise quartz–feldspar ± biotite ± muscovite ± haematite ± amphibole and intervening quartz–feldspar ± biotite schist. The sulphide ore horizons are typically developed within a biotite–muscovite–quartz–kyanite schist, although mineralization locally occurs within internal gneiss units. Contacts between the ore and host rocks are transitional and characterized by a loss of feldspar. Kinematic indicators, such as S-C fabrics and pressure shadows on porphyroblasts, suggest a top to the north shear sense. The sulphides are deformed by a strong shear fabric, enclosed within kyanite or concentrated into low strain zones and pressure shadows around kyanite porphyroblasts. This suggests that the copper mineralization was introduced either syn- or pre-peak metamorphism. In addition to Cu and Co, the ores are also characterized by enrichments in U, V, Ni, Ba and S and small, discrete zones of uranium mineralization, occur adjacent to the hanging wall and footwall of the copper ore bodies or in the immediate footwall to the copper mineralization. Unlike typical Copperbelt mineralization, unmineralized units show very low background copper values. Whole rock geochemical analyses of the interlayered schist and ore schist, compared to the gneiss, show depletions in Ca, Na and Sr and enrichments in Mg and K, consistent with replacement of feldspar by biotite. The mineral chemistry of muscovite, biotite and chlorite reflect changes in the bulk rock chemistry and show consistent increases in X Mg as the schists develop. δ34S for copper sulphides range from +2.3?‰ to +18.5?‰, with pyrite typically restricted to values between +3.9?‰ and +6.2?‰. These values are atypical of sulphides precipitated by bacteriogenic sulphate reduction. δ34S data for Chimiwungo (Cu + Co) show a broader range and increased δ34S values compared to the Malundwe (Cu) mineralization. The Lumwana deposits show many characteristics which distinguish them from classical Copperbelt mineralization and which suggests that they are formed by metasomatic alteration, mineralization and shearing of pre-Katangan basement. Although this style of mineralization is reported elsewhere in the Copperbelt, sometimes associated with the more widely reported stratiform ores of the Lower Roan, none of the previously reported occurrences have so far developed the tonnages of ore reported at Lumwana.  相似文献   

3.

The geology, stable isotopes and fluid inclusions from mineralized and unmineralized Middle Proterozoic sequences of the McArthur Basin, Northern Territory, have been studied at Eastern Creek, Bulman Mines, Beetle Springs, and other localities in the McArthur Basin where disseminated sulphides in unmineralized black shales were available from drill core. At Eastern Creek, galena and minor chalcopyrite (δ34S+3.6 to +11.2%o) occur in an evaporitic sedimentary sequence. Barite (δ34S+18.4 to +24.7%o) also occurs, and saline brines are trapped along healed fractures in the barite. Pressure‐corrected trapping temperatures in the barite (95–138°C), and in vein dolomite (158–168°C) agree with temperature estimates from the degree of maturation of the sedimentary organic matter. The δ18O and δ13CCo2 values of the mineralizing fluid were calculated to be +3.5 to +4.5%o and ‐2.7%o, respectively. Sedimentary dolomite has restricted δ13C and δ18O ranges, within the reported ranges for non‐mineralized Middle Proterozoic dolomite. An ore formation model developed for Eastern Creek, in which a basinal fluid at about 200°C carrying base metals and sulphide was released from underlying sediments during local fault movement, may be applicable to a number of other deposits. The mineralization deposited from these fluids occurs only below the pre‐Roper Group unconformity, implying that it may be older than the basal Roper Group. The δ34S values of iron sulphides in fine grained black dolostones (not associated with mineral deposits) from the McArthur Basin were assessed in the light of the values found for sulphides in modern organic‐rich sedimentary environments. The data so obtained suggest that the considerable concentration of iron sulphide in the mineral deposits formed, at least in part, from heated basinal waters and that disseminated iron sulphides remote from mineralization also formed from a similar source.  相似文献   

4.
Most sulphides from various rock types and mineralization of Archean age exhibit sulphur isotope values (δ34S) near 0‰. This is due to a general absence of conditions suitable for the oxidation-reduction reactions essential for isotopic fractionation. However, some important occurrences of Archean Au mineralization do display significant variations in δ34S). One such occurrence with unusual isotopic compositions is the Hemlo gold deposit: pyrite from the ore typically has δ34S < −6‰ to a minimum value of −17.5‰ The isotopic composition of the pyrite is correlated with the content of Au, indicating that they are genetically related.The sulphur isotope data suggest that sulphur compounds experienced redox reactions in the hydrothermal system at Hemlo and that sulphate was present prior to the Au mineralization. This sulphate may be of exogenic origin from a restricted basin, or of endogenic origin from magmatic-hydrothermal fluids. Other characteristic features of the deposit, such as enrichment in Sb, Tl and Hg, may also be explained by ore deposition under moderately oxidizing conditions.Distinctive δ34S values were also observed in pyrite from Au mineralization at Heron Bay, 30 km west of Hemlo, and from baritic strata 21 to 27 km west and on approximate strike from Hemlo. These occurrences also represent sulphate-bearing hydrothermal systems and, as such, give distant information on the unusual environment of the mineralization at Hemlo. Since the isotopes of sulphur are sensitive to oxidation conditions they may be used to identify hydrothermal activities characteristic of this type of Au mineralization and to explore for other unusual areas of sulphate accumulation in Archean terrains.  相似文献   

5.
Luiswishi is a Congo-type Neoproterozoic sediment-hosted stratiform Cu–Co ore deposit of the Central Africa Copperbelt, located northwest of Lubumbashi (DRC). The ores form two main Cu–Co orebodies hosted by the Mines Subgroup, one in the lower part of the Kamoto Formation and the other at the base of the Dolomitic Shales Formation. Sulphides occur essentially as early parallel layers of chalcopyrite and carrolite, and secondarily as late stockwork sulphides cross-cutting the bedding and the early sulphide generation. Both types of stratiform and stockwork chalcopyrite and carrolite were systematically analyzed for sulphur isotopes, along the lithostratigraphic succession of the Mine Series. The quite similar δ34S values of stratiform sulphides and late stockwork sulphides suggest an in situ recrystallization or a slight remobilization of stockwork sulphides without attainment of isotopic equilibrium between different sulphide phases (chalcopyrite and carrolite). The distribution of δ34S values (−14.4‰ to +17.5‰) combined with the lithology indicates a strong stratigraphic control of the sulphur isotope signature, supporting bacterial sulphate reduction during early diagenesis of the host sediments, in a shallow marine to lacustrine environment. Petrological features combined with sulphur isotopic data of sulphides at Luiswishi and previous results on nodules of anhydrite in the Mine Series indicate a dominant seawater/lacustrine origin for sulphates, precluding a possible hydrothermal participation. The high positive δ34S values of sulphides in the lower orebody at Luiswishi, hosted in massive chloritic–dolomitic siltite (known as Grey R.A.T.), fine-grained stratified dolostone (D.Strat.) and silicified-stromatolitic dolomites alternating with chloritic–dolomitic silty beds (R.S.F.), suggest that they were probably deposited during a period of regression in a basin cut off from seawater. The variations of δ34S values (i.e. the decrease of δ34S values from the Kamoto Formation to the overlying Dolomitic Shales and then the slight increase from S.D.2d to S.D.3a and S.D.3b members) are in perfect agreement with the inferred lithological and transgressive–regressive evolution of the ore-hosting sedimentary rocks [Cailteux, J., 1994. Lithostratigraphy of the Neoproterozoic Shaba-type (Zaire) Roan Supergroup and metallogenesis of associated stratiform mineralization. In: Kampunzu A.B., Lubala, R.T. (Eds.), Neoproterozoic Belts of Zambia, Zaire and Namibia. Journal of African Earth Sciences 19, 279–301].  相似文献   

6.
The Navia gold belt is located in the West Asturian-Leonese Zone of the Iberian Variscan Orogen. The host rocks of the mineralization are quartzites, sandstones and black shales of Cambro-Ordovician age. The gold belt extends along 35 km and has five major veins: Penedela, Encarnita, Fornaza, Carmina and S. Jose. The ores belong to at least four associations having contrasting mineralogies and textures. The δ34S values for individual mineral phases reflect the polyphase metallogenic history. The older association (Stage 1) is Fe-Mn-rich and is made up of spessartine, grunerite-dannemorite and quartz, with magnetite, pyrrhotite and chalcopyrite as metallic phases. The mineralization of Stage 1 is followed by the As-rich Stage 2 with quartz, arsenopyrite and pyrite. The δ34S values for pyrite range from 14.9 to 19.9 per mil (n = 16), and for arsenopyrite from 13.2 to 17.3 per mil (n = 7). The observed isotopic homogeneity likely implies isotopic equilibrium at the scale of the gold vein. Stage 3 contains a coarse-grained base metal sulphide-rich association. The δ4S values for sphalerite range from 16.4 to 20.6 per mil (n= 16), and for galena from 17.0 to 18.7 per mil (n = 11). δ34Ssp > δ34Sgl suggests that the sulphur isotopic fractionation of the ore-forming system had reached equilibrium. The youngest crosscutting mineral association (Stage 4) consists of Pb-Sb sulphosalts, bornite, electrum and quartz. The δ34S values for sulphosalts range from 9.7 to 15.8 per mil, showing the lightest results of the Navia sulphides.The relatively tight clustering of δ34S values of the Au-related sulphides, and the results of fluid inclusions and paragenetic studies, can be interpreted to indicate that the hydrothermal fluids of the last three stages were dominated by H2S. In the H2S predominant field, sulphide minerals precipitating from solutions would exhibit δ34S values similar to the δ34SΣS value of the ore fluid. The heavy δ34SΣS of the Navia fluids is consistent with leaching of sulphur from the host rocks. The main sulphur source could be diagenetic pyrite from the siliciclastic rocks of the Cabos and Luarca Formations, which exhibit δ34S values from 8.3 to 21.2 per mil. An additional sulphur-source in Stage 3 would be the leaching of disseminated sphalerite and galena present in Cambrian carbonates.  相似文献   

7.
Fourteen stratiform, stratabound and vein-type sulphide occurrences in the Upper Allochthon of the Central–North Norwegian Caledonides have been studied for their sulphur, oxygen and hydrogen isotope composition. Depositional ages of host rocks to the stratabound and stratiform sulphide occurrences range from 590 to 640?Ma. The sulphides and their host rocks have been affected by polyphase deformation and metamorphism with a peak temperature of 650?°C dated to 432?Ma. A total of 104 sulphide and 2 barite samples were analysed for δ34S, 16 whole-rock and quartz samples for δ18O and 12 samples of muscovite for δD. The overall δ34S values range from ?14 to +31‰ with the majority of sampled sulphides lying within a range of +4 to +15‰. In most cases δ34S within each hand specimen behaves in accordance with the equilibrium fractionation sequence, δ34Sgn<δ34Scp<δ34Ssph<δ34Spy. A systematic increase in δ34S from the vein sulphides (?8‰) through schist/amphibolite-hosted (+6‰) and schist-hosted (+7 to +12‰) to dolomite-hosted (+12 to +31‰) occurrences is documented. The δ34S averages of the stratiform schist-hosted sulphides are 17 to 22‰ lower than in the penecontemporaneous seawater sulphate. The Bjørkåsen (+4 to +6‰) occurrence is a volcanogenic massive sulphide (VMS) transitional to sedimentary massive sulphide (SMS), exhalative, massive, pyritic deposit of Cu–Zn–Pb sulphides formed by fluids which obtained H2S via high-temperature reduction of seawater sulphate by oxidation of Fe2+ during the convective circulation of seawater through underlying rock sequences. The Raudvatn, volcanic-hosted, disseminated Cu sulphides (+6 to +8‰) obtained sulphur via a similar process. The Balsnes, stratiform, ‘black schist’-hosted, pyrite–pyrrhotite occurrence (?6 to ?14‰) is represented by typical diagenetic sulphides precipitated via bacteriogenic reduction of coeval (ca. 600?Ma) seawater sulphate (+25 to +35‰) in a system open to sulphate supply. The δ34S values of the Djupvik–Skårnesdalen (+7 to +12‰), Hammerfjell (+5 to 11‰), Kaldådalen (+10 to +12‰) and Njallavarre (+7 to +8‰) stratiform, schist-hosted, massive and disseminated Zn–Pb (±Cu) sulphide occurrences, as well as the stratabound, quartzite-hosted, Au-bearing arsenopyrite occurrence at Langvatnet (+7 to +11‰), suggest that thermochemically reduced connate seawater sulphate was a principal sulphur source. The Sinklien and Tårstad, stratabound, dolomite- and dolomite collapse breccia-hosted, Zn (±Cu–Pb) sulphides are marked by the highest enrichment in 34S (+20 to +31‰). The occurrences ?are?assigned to the Mississippi-Valley-type deposits.?High δ34S values require reduction/replacement of contemporaneous (ca. 590?Ma) evaporitic sulphate (+23 to +34‰) with Corg-rich fluids in a closed system. The Melkedalen (+12 to +15‰), stratabound, fault-controlled, Cu–Zn sulphide deposit is hosted by the ca. 595?Ma dolomitised Melkedalen marble. The deposit is composed of several generations of ore minerals which formed by replacement of host dolomite. Polyphase hydrothermal fluids were introduced during several reactivation episodes of the fault zone. The positive δ34S values with a very limited fractionation (<3‰) are indicative of the sulphide-sulphur generated through abiological, thermochemical reduction of seawater sulphate by organic material. The vein-type Cu (±Au–W) occurrences at Baugefjell, Bugtedalen and Baugevatn (?8 to ?4‰) are of hydrothermal origin and obtained their sulphur from igneous sources with a possible incorporation of sedimentary/diagenetic sulphides. In a broad sense, all the stratiform/stratabound, sediment-hosted, sulphide occurrences studied formed by epigenetic fluids within two probable scenarios which may be applicable separately or interactively: (1) expulsion of hot metal-bearing connate waters from deeper parts of sedimentary basins prior to nappe translation (late diagenetic/catagenetic/epigenetic fluids) or (2) tectonically driven expulsion in the course of nappe translation (early metamorphic fluids). A combination of (1) and (2) is favoured for the stratabound, fault-controlled, Melkedalen and Langvatnet occurrences, whereas the rest are considered to have formed within option (1). The sulphides and their host rocks were transported from unknown distances and thrust on to the Fennoscandian Shield during the course of the Caledonian orogeny. The displaced/allochthonous nature of the Ofoten Cu–Pb–Zn ‘metallogenetic province’ would explain the enigmatically high concentration of small-scale Cu–Pb–Zn deposits that occur only in this particular area of the Norwegian Caledonides.  相似文献   

8.
Bituminous mud shales of the Upper Permian Ravnefjeld Formation (Zechstein 1 equivalent) are mineralised with zinc, lead and copper within a ca. 50 km2 area on Wegener Halvø in central East Greenland. The occurrence of base-metal sulphides in shale nodules cemented prior to compaction indicates an early commencement of base-metal mineralisation. In other cases, post-compactional sulphide textures are observed. Homogeneous lead isotope signatures of galena and sphalerite from the shales (206Pb/204Pb: 18.440–18.466; 207Pb/204Pb: 16.554–16.586; 208Pb/204Pb: 38.240–38.326) suggest that all base metals were introduced during a single hydrothermal event. Therefore, post-compactional textures are believed to result from recrystallisation of early diagenetic sulphides during deep burial in the Upper Cretaceous to Tertiary. Lead isotope signatures of galena hosted in Upper Permian carbonate build-ups are relatively heterogeneous compared to those of the shale-hosted sulphides. The observed relations indicate a shared lead source for the two types of mineralisation, but different degrees of homogenisation during mineralisation. This suggests that lead was introduced to the carbonate rocks and black shales during two separate events. δ34S of base-metal sulphides in the Ravnefjeld Formation lie between –12 and –4‰, whereas synsedimentary and early diagenetic pyrite in unmineralised shales in general have δ34S between –47 and –16.5‰. Early diagenetic pyrite in the Wegener Halvø area in general has δ34S 15 to 20‰ higher than the same pyrite morphotype in Triaselv in the western part of the basin. This relatively high δ34S can be explained by extensive microbial sulphate reduction within persistent euxinic (super-anoxic) bottom waters under which supply of isotopically light seawater sulphate (and disproportionation of intermediate sulphur compounds) was restricted. The sulphur in the base-metal sulphides is believed to represent sulphide-dominated pore water, enriched in 34S due to preferential removal of 32S by sulphate-reducing bacteria and precipitation of diagenetic pyrite in the near-seafloor environment. We suggest that the sulphide-dominated pore water was trapped in the shale formation prior to introduction of base-metal-bearing fluids through fractures in the underlying carbonates, and that sulphide precipitation took place when the two fluids met. δ34S values of carbonate-hosted base-metal sulphides fall within the same range as the shale-hosted ones. The relationship between barite and sulphides and evidence for pre-mineralisation entrapment of liquid hydrocarbons in the carbonates suggest that the sulphide in this case is derived by in-situ thermochemical sulphate reduction (TSR). Measured fractionation between sulphide and sulphate ranges from 18.5 to 24.4‰, suggesting temperatures of TSR around 70 to 100 °C. Vitrinite reflectance measurements in mineralised shale samples are all between 1.7 and 2.0%, except for samples taken close to a Tertiary dyke giving ca. 3.0%. Vitrinite reflectance data are comparable to previously published data from unmineralised shale samples in the area and could not be proven to correlate with the degree of mineralisation. This indicates that any early hydrothermal effect has been overprinted later, probably during deep burial in the Late Cretaceous to Early Tertiary as previously proposed.  相似文献   

9.
《International Geology Review》2012,54(14):1635-1648
The Koushk zinc–lead deposit in the central part of the Zarigan–Chahmir basin, central Iran, is the largest of several sedimentary–exhalative (SEDEX) deposits in this basin, including the Chahmir, Zarigan, and Darreh-Dehu deposits. The host-rock sequence consists of carbonaceous, fine-grained black siltstone with interlayered rhyolitic tuffs. It corresponds to the upper part of the Lower Cambrian volcano-sedimentary sequence that was deposited on the Posht-e-Badam Block due to back-arc rifting of the continental margin of the Central Iranian Microcontinent. This block includes the late Neoproterozoic metamorphic basement of the Iran plate, overlain by rocks dating from the Early Cambrian to the Mesozoic. Based on ore body structure, mineralogy, and ore fabric, we recognize four different ore facies in the Koushk deposit: (1) a stockwork/feeder zone, consisting of a discordant mineralization of sulphides forming a stockwork of sulphide-bearing dolomite (quartz) veins cutting the footwall sedimentary rocks; (2) a massive ore/vent complex, consisting of massive replacement pyrite, galena, and sphalerite with minor arsenopyrite and chalcopyrite; (3) bedded ore, with laminated to disseminated pyrite, sphalerite, and galena; and (4) a distal facies, with minor disseminated and laminated pyrite, banded cherts, and disseminated barite. Carbonatization and sericitization are the main wall-rock alterations; alteration intensity increases towards the feeder zone. The δ34S composition of pyrite, sphalerite, and galena ranges from?+6.5 to?+36.7‰. The highest δ34S values correspond to bedded ore (+23.8 to?+36.7‰) and the lowest to massive ore (+6.5 to?+?17.8‰). The overall range of δ34S is remarkably higher than typical magmatic values, suggesting that sulphides formed from the reduction of seawater sulphate by bacteriogenic sulphate reduction in a closed or semi-closed system in the bedded ore, whereas thermochemical sulphate reduction likely played an important role in the feeder zone. Sulphur isotopes, along with sedimentological, textural, mineralogical, and geochemical evidences, suggest that this deposit should be classified as a vent-proximal SEDEX ore deposit.  相似文献   

10.
In the Eastern Pontide Region of northeastern Turkey, volcanogenic Cu-Zn-Pb deposits of the Kuroko type are widespread within the dacitic series of the Liassic-Eocene volcano-sedimentary succession. Sulfide mineralization within the studied deposits shows four different depositional styles: disseminated ore; polymetallic stockwork ores; polymetallic massive ores; and disseminated pyrite in the hanging-wall tuff units. Only the stockwork and massive ores are economically important, and usually one or the other dominates in each ore body.

The δ34S of sulfide minerals belonging to the various styles of mineralization are in the range from ?2.6 to +5.2% (VCDT): pyrite has the highest values and the galena lowest values in agreement with the usual isotopic-fractionation trends. Massive ores have heavier sulfur-isotope composition among the mineralization styles and the heaviest values are recorded in barite- and gypsum-rich deposits. The close similarity of the δ34S among the various mineralization episodes in some deposits indicates a single sulfur source having a stable and homogenous composition.

The δ34S of sulfates fall into three groups: barites and primary gypsum (15.4 to 20.4%), close to coeval seawater sulfate; one value of barite (25.4%) heavier than coeval sea water; and values of secondary gypsum (2.2 to 8.0%) either very light compared to coeval seawater sulfate, or within the range recorded from sulfide minerals. The δ34S values of pyrite disseminated in the brecciated dacite tuff units are very close to zero and similar to the ones reported for magmatic rocks, suggesting a magmatic source for the sulfur of the earliest sulfide mineralization episode. These δ34S data are not sufficient to calculate the fraction of the reduced sulfur derived from seawater sulfate, as the associated fractionation factor cannot be constrained.  相似文献   

11.
Measurements of the 34S/32S ratios in sulphides from the slightly metamorphosed Lady Loretta deposit show the sphalerite and galena to be in isotopic equilibrium. Pyrite in immediate association with these sulphides is not isotopically related. A similar distribution of sulphur isotopes had previously been noted in the even less altered McArthur deposit, for which a dual sulphur source was postulated. This fresh isotopic evidence from Lady Loretta now suggests that such a genesis for stratiform sulphides from the Proterozoic is not uncommon.  相似文献   

12.
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.  相似文献   

13.
Thermal water samples and related young and fossil mineralization from a geothermal system at the northern margin of the Upper Rhine Graben have been investigated by combining hydrochemistry with stable and Sr isotope geochemistry. Actively discharging thermal springs and mineralization are present in a structural zone that extends over at least 60 km along strike, with two of the main centers of hydrothermal activity being Wiesbaden and Bad Nauheim. This setting provides the rare opportunity to link the chemistry and isotopic signatures of modern thermal waters directly with fossil mineralization dating back to at least 500–800 ka. The fossil thermal spring mineralization can be classified into two major types: barite-(pyrite) fracture filling associated with laterally-extensive silicification; and barite, goethite and silica impregnation mineralization in Tertiary sediments. Additionally, carbonatic sinters occur around active springs. Strontium isotope and trace element data suggest that mixing of a hot (>100 °C), deep-sourced thermal water with cooler groundwater from shallow aquifers is responsible for present-day thermal spring discharge and fossil mineralization. The correlation between both Sr and S isotope ratios and the elevation of the barite mineralization relative to the present-day water table in Wiesbaden is explained by mixing of deep-sourced thermal water having high 87Sr/86Sr and low δ34S with shallow groundwater of lower 87Sr/86Sr and higher δ34S. The Sr isotope data demonstrate that the hot thermal waters originate from an aquifer in the Variscan crystalline basement at depths of 3–5 km. The S isotope data show that impregnation-type mineralization is strongly influenced by mixing with SO4 that has high δ34S values. The fracture style mineralization formed by cooling of the thermal waters, whereas impregnation-type mineralization precipitated by mixing with SO4-rich groundwater percolating through the sediments.  相似文献   

14.
Mineral assemblages present within the Charmitan gold(-tungsten) quartz-vein mineralization have been investigated for their cathodoluminescence behaviour, chemical composition and noble gas isotope systematics. This inventory of methods allows for the first time a systematic reconstruction of the paragenetic relationships of quartz, scheelite, sulphides and native gold within the gold mineralization at Charmitan and provides the basis to utilise noble gas data in the discussion of sources and evolution of ore-forming fluids. The vein quartz is classified into four generations based on microscopic and cathodoluminescence investigations. Quartz I shows intense brittle deformation as associated scheelite I. Undeformed scheelite II overgrows scheelite I and has lower light rare earth element and higher intermediate rare earth element contents as well as higher strontium concentrations. Scheelite II is associated with the economic gold mineralization and formed during re-crystallisation and re-precipitation of material which was partly re-mobilised from early scheelite I during infiltration of gold-bearing fluids. Early stage native gold inclusions are often associated with stage 2 sulphides, scheelite II and bismuth tellurides and contain Ag (3.6–24.4 wt.%), Hg (≤1.0 wt.%) and Bi (≤0.2 wt.%). Later stage electrum grains occur in association with stage 3 sulphides and sulphosalts and contain Hg (<0.8 wt.%) and elevated Sb concentrations (up to 3.0 wt.%). Noble gas isotope data (3He/4He: 0.2-0.4 Ra) for hydrothermal ore fluids trapped in the gold-related sulphides and sulphosalts (stage 2 pyrite and arsenopyrite; stage 3 pyrite, sphalerite, galena and lead sulphosalts) suggest that diverse fluid sources were involved in the formation of the Charmitan gold deposit. These data are indicative of a small, but significant input of fluids from external, deep-seated (mantle and possibly lower crust) sources. A decrease in the input of mantle helium and an increasing role of crustal helium from early to later stages of the mineralization is suggested by the measured 3He/4He and 40Ar*/4He ratios. Sulphides from ore veins in meta-sedimentary rocks contain higher portions of meteoric fluids than those in intrusive rock types as indicated by their lower 3He/36Ar ratios. The 3He/36Ar ratios in the meta-sedimentary rocks agree well with ratios typical of gold mineralizations in the Tien Shan gold province completely hosted by meta-sedimentary sequences, indicating intense fluid-wall rock interaction.  相似文献   

15.
Rhythmic copper sulphide bands occur in the Weissliegendes sandstones, in the footwall of the Kupferschiefer in the mining district of SW Poland. The δ 34S values of sulphides vary from −39 to — 44‰ (6–7‰ lighter than Kupferschiefer sulphides). The copper sulphides are represented mainly by digenite and chalcocite. According to microprobe results their Pb, Ni, Zn and Ag contents are similar to those in the Kupferschiefer. The bands are assumed to be formed by diffusion of bacterially produced hydrogen sulphide from the Kupferschiefer into the porous volume of the white sandstones containing dissolved copper. The sulphides were precipitated in almost equidistant bands, from top to bottom, probably according to the Ostwald-Prager supersaturation theory. The increase of isotopically heavier sulphur towards the lower levels in the sandstone might be explained by closing of the bacterial sulphate reduction system. Contribution to the IGCP Project No. 254  相似文献   

16.
An integrated mineralogical-geochemical and stable isotopic study of Pb-Zn deposits located at Kayar-Ghugra (Zn-Pb ± Ag), Rampura-Agucha (Zn-Pb, Ag), Dariba-Bethumni (Zn-Pb) and Zawar (Pb-Zn ± Cd, Ag) in Rajasthan is presented in this paper. The Kayar Zn-Pb deposit hosted by (i) phlogopite-tremolite bearing dolomitic carbonates and (ii) scapolite bearing calc-silicates, both belonging to Mesoproterozoic Delhi Supergroup exhibit distinctly different δ13C signatures being close to zero permil for the former reflecting deposition in pristine marine environment and much depleted isotopic values for the latter possibly related to post-depositional alterations. The Zn-Pb sulphides of Agucha, hosted in amphibolite facies to lower granulite facies metasedimentary units belonging to the Bhilwara Supergroup have δ34S values that indicate (i) H2S dominated regime characterized by low fO2, low pH, wherein the δ34S(fluid) responsible for mineralisation approximates the δ34S(sulphide); (ii) the role of seawater in the generation of Agucha ores; (iii) the process of a low temperature oxidation of sulphides in the hydrothermal fluids resulting in the formation of sulphate, by the interaction of ground water; (iv) isotopic disequilibrium in sulphatesulphide pairs that explain oxidation of H2S by acid groundwater (low pH) and deposition of sulphides at higher temperatures and (v) equilibrium isotopic fractionation of the coexisting sulphides reflecting in a higher concentration of H2S (>10?5m) in relation to the total metal content in the hydrothermal fluid $\left( {m_{H_2 S} \geqslant mS_{_{metals} } } \right)$ . Accordingly the concentration of sulphide-sulphate in the hydrothermal solution responsible for the mineralization in Agucha exceeds that of total metals. The sulphides of Bethumni-Rajpura-Dariba belt hosted in low to medium grade siliceous carbonates has a marginally positive (mean of +1.5‰) δ13C values. At Sindeswar, broad and widely scattered δ34S values indicate a polymodal sedimentary source of sulphur that recrystallised at rather low temperature of < 50°C possibly during the processes of low temperature bacterial reduction. The C and O-isotopic studies on mineralized and non-mineralized carbonates reveal (i) normal marine depositional signatures for non-mineralized carbonates with possible minor influence of biogenic carbon during deposition and (ii) ore zone carbonates exhibit depleted δ13C values presumably due either to the deeper mantle-like source of carbonates or due to post-depositional equilibration with isotopically light meteoric waters. In Zawar belt, sulphides hosted in dolomitic carbonate indicated (i) near identical δ34S values of disseminated galena and pyrite veinlets and depleted values of ?4.6 ‰ for late veins of massive galena of Zawar Mala (ii) pyritepyrrhotite veinlet having enhanced δ34S values when compared to the PbS-ZnS veinlet in Morchia-Magra, Balaria and Baroi mines. The carbon isotopic values for carbonates of Zawar Mala mine area are mostly depleted and those from Balaria and Baroi mines exhibit values of 13C close to zero. The generally depleted δ 18O clustering around ?15 ‰ tally well with the reported Paleoproterozoic carbonates and is attributed to the post-depositional equilibration reactions with isotopically light meteoric waters. It is summarized that the host carbonates for Zn-Pb deposits occurring in different tectono-stratigraphic units in Rajasthan have largely similar but bimodal distribution of δ 18O and δ13C isotopic ratios that suggest normal marine values and much depleted values. Whereas the former seems to be in general agreement with the nature of distribution in the Palaeoproterozoic carbonates the latter is attributed to (i) depositional conditions of the basins that includes absence or presence of biogenic activity (ii) isotopic re-equilibration under different metamorphic recrystallization events and/or (iii) interaction with isotopically lighter meteoric waters. In contrast to the uniformity in the C and O distribution pattern, the S-isotopic distribution in the deposits of Rampura-Agucha, Bethumni-Rajpura-Darbia and Zawar mine areas show marked variations reflecting complex deposit-specific ore-forming processes in the said deposits.  相似文献   

17.
The Shaki porphyry copper(gold) deposits are a trpical example of porphyry copper deposits associ-ated with diorite in eastern China. Quartz diorite, which hosts the deposits, has a Rb-Sr isochron age of 127.9±1.6Ma. Geochemically, the rock is rich in alkalis (especially sodium), light rare earth elements (LREE) and large-ionlithophile elements (LILE), and has a relatively low initial strontium isotopic ratio (I_(Sr)=0.7058); thus it is the productof differentiation of crust-mantle mixing source magma. The model of alteration and mineralization zoning is similarto the Hollister (1974) diorite model. The ore fluids have a relatively high salinity and contain significant amounts ofCO_2, Ca~(2+), Na~+ and Cl~-. The homogenization temperatures of fluid inclusions for the main mineralization stage rangefrom 280 to 420℃, the δ~(18)O values of the ore fluids vary from 3.51 to 5.52‰, the δD values are in the range between-82.4 and -59.8‰, the δ~(34)S values of sulphides vary from -0.3 to 2.49‰, and the δ~(13)C values of CO_2 in inclusionsrange between -2.66 and -6.53‰. Isotope data indicate that the hydrothermal ore fluids and ore substances of theShaxi porphyry copper (gold) deposits were mainly derived from magmatic systems.  相似文献   

18.
The sulphur isotope composition of 233 sulphides and 40 sulphates has been investigated and evaluated in combination with 29 earlier published data. The total variation of δ34S values for the sulphides and the sulphates ranges from ?40 up to ?1 ‰ and from +7 up to +20 ‰, respectively. For the mineral species the variations are (with number of samples in brackets): galena (96) ?32 up to ?2 ‰, sphalerite (141) ?30 up to ?4 ‰, marcasite (16) ?27 up to ?1 ‰, pyrite (10) ?26 up to ?13 ‰, molybedenite (3) ?40 up to ?29 ‰, anhydrite and gypsum (8) +15 up to +20 ‰, coelestine (1) +19 ‰, and barite (33) +7 up to +18 ‰. The frequency distribution of the δ34S values corresponds with the complexity of the ore forming processes which resulted in six strata-bound ore mineralizations. The sulphate values clearly show that the sulphate sulphur originates from sea water sulphate. The sulphides are formed by bacteriogeneric processes from seawater sulphate, and their sulphur isotope composition depends on the lithofacies of the sediments as well as on the following diagenetic processes.  相似文献   

19.
The Shamrocke ore body is a stratiform deposit of disseminated copper-iron sulphides found within lenses of calcareous meta-arkose occurring in Lomagundi Group graphitic schist (Late Precambrian) at Karoi, Rhodesia. Both sulphides and sediments were subjected to high grades of regional metamorphism. Argon/argon isochron ages indicate a major metamorphic event at 550 m. y. (Damaran orogeny) with later minor argon losses. Ore sulphide 34S values range from +3.0 to +14.8 CDT and a general decrease from footwall to hanging-wall reflects an original sedimentary environment where sulphides formed about the sea bed from hydrothermal fluids progressively mixing with sea water. Isotopically lighter sulphides formed syngenetically in the host rocks from bacterial reduction of sulphate. The pyrrhotite was probably formed from pyrite during metamorphism, and owing to reducing conditions maintained similar 34S values to the original pyrite. Oxygen and carbon isotopic analyses of mineralised and unmineralised carbonate lenses are consistent with deposition as marine limestones in an evaporitic environment and/or near hot spring vents.I. N. S. Contribution No 734  相似文献   

20.
《Applied Geochemistry》2005,20(2):261-274
Very low concentrations of total S, mainly sedimentary sulphides, were quantitatively extracted from Quaternary sands of the Elbe Basin, using HNO3, Br2 and HCl, to distinguish 3 aquifer zones:
  • •an upper aerobic section, containing low concentrations (only a few ppm) of non-sulphidic S compounds,
  • •the central and lower part of the aquifer, dominated by 34S-depleted sedimentary Fe sulphides, formed by reduction of infiltrating SO4, derived from groundwater recharge, and
  • •the lowest 5–10 m of the aquifer, containing high concentrations of 34S-enriched sulphides.
The latter originated from dissolved Zechstein SO4, which was reduced during upwelling through the organic-rich Tertiary aquiclude. H2S and HS− reacted and precipitated with Fe and other metal ions shortly after migration into the Corg-poor Quaternary aquifer. The sulphides yield valuable information concerning the ascent of confined saline solutions from isolated Zechstein evaporites inside the “Mühlberger Graben”, which is covered by Cenozoic sediments and whose extension and boundaries are therefore not well defined. Only a few locations, close to faults and geological windows, show deep-water admixture sufficiently strong to cause visible changes in hydrochemistry and isotopic ratios of SO4 and DIC directly above the base of the Quaternary. Sulphides showing different origins may possibly be used in other areas to provide information concerning underlying geology and hydrodynamics.  相似文献   

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