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1.
Kuroko-type massive sulfide deposits of the Eastern Black Sea province of Turkey are related to the Upper Cretaceous felsic lavas and pyroclastic rocks, and associated with clay and carbonate alteration zones in the footwall and hangingwall lithologies. A complete upward-vertical section of a typical orebody consists of a stringer-disseminated sulfide zone composed mainly of pyrite and chalcopyrite; a massive pyrite zone; a massive yellow ore consisting mainly of chalcopyrite and pyrite; a black ore made up mainly of galena and sphalerite with minor amounts of chalcopyrite, bornite, pyrite and various sulfosalts; and a barite zone. Most of the deposits in the province are associated with gypsum in the footwall or hangingwall. The paragenetic sequence in the massive ore is pyrite, sphalerite, chalcopyrite, bornite, galena and various sulfosalts, with some overlap between the mineral phases. Massive, stringer and disseminated sulfides from eight kuroko-type VMS deposits of the Eastern Black Sea province have a 34S range of 0–7 per mil, consistent with the 34S range of felsic igneous rocks. Sulfides in the massive ore at Madenköy (4.3–6.1 per mil) differ isotopically from sulfides in the stringer zone (6.3–7.2 per mil) suggesting a slightly increased input of H2S derived from marine sulfate with time. Barite and coarse-grained gypsum have a 34S range of 17.7–21.5 per mil, a few per mil higher than the 34S value of contemporaneous seawater sulfate. The deposits may, therefore, have formed in restricted basins in which bacterial reduction of sulfate was taking place. Fine-grained, disseminated gypsum at Kutlular and Tunca has 34S values (2.6–6.1 per mil) overlapping those of ore sulfides, indicating sulfide oxidation during waning stages of hydrothermal activity.  相似文献   

2.
The Felbertal scheelite deposit is the largest known strata-bound tungsten concentration. It lies in an up to 400 m thick rock pile in the lowermost part of the volcanic rock sequence, probably of the Early Paleozoic Habach Formation. Both ore fields (eastern and western) have been affected by Variscan and Alpine metamorphism and tectonism, resulting in a remobilization of the ore mineralization. This ore deposit and the neighboring rocks show a strikingly low sulfur content. The eastern field with one major orebody has very little sulfide mineralization. The western field, with 8 orebodies (K1–K8) and two remobilized vein zones (S1 and S2), reveals somewhat more minor sulfide enrichments that are mainly within and around the K1 and K2 orebodies and in some parts of the interlayered schist sequence. Sulfur isotope compositions of 90 sulfide minerals (37 pyrrhotite, 20 chalcopyrite, 19 pyrite and 11 molybdenite and/or WS2-MoS2 solid solutions and 3 Pb-Bi sulfosalts, including 7 sulfides within scheelite grains) from 60 ore and host rock samples have been determined with a standard error of less than ±0.2 per mil. All data range from –3.6 to +4.3 34S. There are small differences in the sulfur isotope values from place to place and in time from the first and second to the third generation. In the western field, the K1 orebody differs from other orebodies (K2, K4, K7) due to isotopically heavier 34S values. The three scheelite generations show differences in the 34S values of the sulfide microphases within scheelite grains, from +1.0 to +4.3 per mil for the first and the second, and from –1.8 to –3.3 per mil for the third generation. Sulfide phases within molybdoscheelites may have crystallized under the same conditions as the other coeval sulfide minerals in the same orebody. They commonly formed later than scheelite. These changes may be explained using data from Ohmoto and Rye (1979): Small changes in temperature, pH, and/or may result in large changes in the 34S values with the precipitation of isotopically heavier sulfides under more reducing conditions. Only four samples with sulfide mineral pairs show isotopic equilibrium. All others display some disequilibrium. We suggest that the sulfides in the ores and surrounding volcanogenic host rocks formed contemporaneously from the same hydrothermal ore fluids, and that the sulfur species in these fluids may have been dominantly H2S.  相似文献   

3.
Sulfide minerals in amounts up to 3 vol% are found in basal, chilled marginal zones of two layered peridotite-pyroxenite-gabbro sills in the Early Precambrian Deer Lake Complex, northcentral Minnesota. The sulfides occur interstitially to silicate minerals, and consist of pyrrhotite with minor exsolved cobaltian pentlandite, chalcopyrite, gersdorffite, and marcasite±pyrite as an alteration product of pyrrhotite.The basal chilled units (3–6 m) of the sills are divisable into three zones based primarily on textures. The lowermost zone is an equigranular basalt, whereas the overlying zone is characterized by skeletal, spinifex-like actinolite after clinopyroxene. The upper zone of the basal margins contains elongate and swallow tail plagioclase, and is barren of sulfide minerals.Electron microprobe analyses of sulfide minerals and modal data suggest that sulfide bulk compositions at 1,100–1,000 ° C represent a pyrrhotite solid solution and a coexisting Cu-rich sulfide liquid. Cooling of the Cu-rich liquid and low temperature transformations are thought to have produced chalcopyrite or chalcopyrite plus pyrrhotite. The sulfide minerals have reequlibrated to temperatures near 300 ° C or less.Analyses of sulfur content and 34S values suggest that assimilation of sulfur from adjacent country rocks was the principal mechanism responsible for anomalous concentrations of sulfides in the basal chilled margins. The distribution of sulfides in the peridotite-pyroxenite-gabbro portions of the sills, and calculations of settling rate preclude an origin involving gravitational settling of immiscible droplets through the magma body.  相似文献   

4.
The economic mineralization of Pd at the Lac des Iles mine occurs in the gabbroic rocks of the Mine Block Intrusion in the 2.69 Ga Lac des Iles Intrusive Complex. The complex intruded the tonalitic rocks of the Lac des Iles greenstone belt in the Wabigoon Subprovince of the Superior Province of Canada. We conducted a detailed study on the Pd mineralization in the southern Roby Zone and the Twilight Zone. Sulphide minerals commonly display exsolution textures where pentlandite and chalcopyrite are exsolved from pyrrhotite. Sulphur contents from these zones display positive correlations with the contents of platinum group elements (PGE), Se, and Te, suggesting a magmatic origin of the mineralization where PGE were concentrated in immiscible sulphide melt in the parental magmas. The average ratios of Se/S (703±192×10–6) and Te/S (192±104×10–6) in the two zones are higher than the primitive mantle values of ~300×10–6 and ~48×10–6, respectively. The high ratios are consistent with the derivation of their parental magmas from a depleted mantle source. The High Grade Zone forms a narrow northwest-trending zone in the margin of the Roby Zone, and is hosted by an intensely altered clinopyroxenite/melanogabbroic unit. It contains two mineral assemblages; millerite + siegenite ± chalcopyrite ± pyrite co-existing with hornblende + plagioclase ± quartz ± carbonate, and pyrite ± chalcopyrite with chlorite + actinolite ± albite ± quartz ± carbonate. The ore is high in Pd (mean Pd/Pt ratio of 16.5; up to 25) compared to the southern Roby Zone and Twilight Zone where the Pd/Pt ratios are ~8. It shows positive correlations between Se and Te and between Se and immobile metals, such as Ni and Co. The data suggest a primary magmatic origin of mineralization of the High Grade Zone, but there is substantial scatter on diagrams involving S, such as the plot between S and Se. The evidence suggests that the primary magmatic mineralization was followed by hydrothermal transport of mobile elements. Using the relationships between Se and metals, the ore most likely had 0.8–2 ppm Pt and 8–21 ppm Pd during the primary mineralization. The subsequent hydrothermal activity resulted in the enrichment of Pd by up to 40 ppm. The lack of fluid pathways in the High Grade Zone and the distribution of the zone are consistent with magmatic-hydrothermal activity by aqueous fluids exsolved from the parental magmas of the Roby Zone and High Grade Zone. Sulphide minerals from the southern Roby Zone, Twilight Zone, and High Grade Zone have similar 34S values, ranging from 0.0 to +1.5. The data are consistent with the derivation of S from the mantle. In individual samples from the southern Roby Zone and High Grade Zone, pyrite shows lower 34S than chalcopyrite, suggesting isotopic disequilibrium of S. This likely reflects the crystallization and re-crystallization of sulphide minerals over a wide range of temperatures.Editorial handling: B. Lehmann  相似文献   

5.
A sulfur isotopic study of the San Cristobal tungsten-base metal mine,Peru   总被引：1，自引：0，他引：1  
The San Cristobal tungsten-base metal deposit differs from other quartz-wolframite vein deposits in that it has a major period of base metal mineralization consisting of pyrite, chalcopyrite, sphalerite, and galena. Homogenization temperatures of primary and pseudosecondary inclusions were measured in augelite (260–400°C), quartz (230–350°C) and sphalerite (180–220°C). The 34S values of H2S in solution in equilibrium with the vein minerals range from 1.6 to 9.0 permil increasing through the paragenesis. The relatively heavy values suggest a nonmagmatic source for the sulfur. Evaporitic sulfates are a likely source of heavy sulfur and sedimentary anhydrite is known to occur near the San Cristobal region. In contrast to San Cristobal are three similar quartz-wolframite vein deposits, Pasto Bueno, Panasqueira, and Tungsten Queen. They each have an average 34S value for sulfides of about 0 permil, suggesting a sulfur of magmatic origin. At San Cristobal an influx of sedimentary sulfur could not only account for the distinctive isotopic signature of the sulfides but also for the presence of the base metal mineralization.  相似文献   

6.
M. Deb 《Mineralium Deposita》1986,21(4):313-321
The sulfur isotope composition of 86 sulfide minerals from the Middle Proterozoic, metamorphosed, stratiform, sediment-hosted Zn-Pb-CU sulfide deposits of Dariba and Sindeswar Kalan located within the Rajpura-Dariba belt in Rajasthan, NW India, have been determined. In addition, 16 carbonaceous and 2 carbonate rock samples from the ore zone have been analyzed for their Ctot and Corg contents and carbon isotope compositions. The sulfur isotope compositions range from 9.1 to –6.7 (mean value of 1.9). Increasing 34S values stratigraphically upward are observed, particularly for pyrite and pyrrhotite suggesting a syngenetic origin for the sulfur. No marked lateral isotopic variations or isotopic variation in minerals from successive laminae in banded ore samples occur. Fractionation of sulfur isotopes between coexisting sulfides suggests that the original isotopic pattern was basically preserved during the amphibolite-facies metamorphism suffered by the deposits. Corg in carbonaceous rocks ranges 0.5–9.3 wt%, with 13C values between –21 and –31 (mean of –25.4) in keeping with the biogenic derivation of the carbon. Recrystallized dolostones have 13C values close to –14.4Geological evidence and isotopic features are consistant with the following genetic scheme: (a) base-metal ores along the belt formed from geothermal emanations carrying H2S, produced by the chemical reduction of seawater sulfates and leaching of mafic volcanics, in a semiclosed (with respect to SO4), shallow-water, rift-related basin with high biological activity; (b) pyrite and pyrrhotite formed diagenetically by bacterial reduction of sulfate in pore seawater in a system open to H2S, thus bringing about the gradual enrichment of 34S in these minerals stratigraphically upward; and (c) northward in the belt, at Sindeswar Kalan, the basin of ore deposition was relatively more open.  相似文献   

7.
Sulphur isotopic compositions of sulphides within garnet-rich rocks and high-grade ore from the Broken Hill deposit, New South Wales, Australia, have been determined and show a range of values of –3.3 to +6.7 per mil. Thermochemical considerations, including the spread of values of 34S, suggest that the deposit was derived from a mixed source of sulphur in which seawater, reduced by inorganic processes, mixed with magmatic sulphur or that sulphate from contemporaneous seawater was reduced biogenically at low temperatures. Thermochemical considerations also suggest that pyrrhotite formed by desulphidation of pyrite so that the original Fe-S-O assemblage was pyrite ± magnetite.34S measurements show a broad range which is considered to be due to isotopic reequilibration during retrograde metamorphism and analytical and sampling technique. These data should not be used to indicate original temperatures of deposition or metamorphic temperatures associated with the various metamorphic events.  相似文献   

8.
The S-isotopic compositions of sulfide deposits from Steinmann, granitoid and felsic volcanic associations have been examined. Ores of Steinmann association have 34S values close to zero per mil (34S=+0.3±3.1) it appears they are of mantle origin. Isotopically, ores of granitoid association regularly show a variable enrichment in 32S relative to meteoritic (34S=–2.7±3.3). The composition is in accord with an upper mantle/lower crustal source. Two stratiform accumulations of felsic volcanic association show a narrow spread of 34S values (+0.2 to 2.4); a mantle origin for the sulfur in these deposits is favored. In contrast, vein, stockwork and cement ores are moderately enriched in 32S relative to meteoritic (34S=–4.0±6.4). These ores are polygenetic; sulfur and metals appear to have been leached from local country rocks where volcanogenic and biogenic sulfur predominate.  相似文献   

9.
Abstract: Dashuigou, a unique tellurium‐dominated deposit over the world, is located in the western margin of the Yangtze cra‐ton in southwestern China. It is characterized by high‐grade tellurium accompanied by bismuth, gold, silver, and sulfur, and occurs in the area of less than one km2. The mineralization is divided into three stages, i.e. (1) tellurium‐bearing pyrrhotite–pyrite stage, (2) tetradymite stage, and (3) auriferous quartz veins stage. Tellurium mineralization coexisting with bismuth, silver, selenium, and gold predominantly develops in the stage 2, while the stage 1 is enriched only in sulfur and iron, and the stage 3 is very weakly mineralized with gold. The δ34S values of sulfides in the ore of the deposit vary in a narrow range of –3.1 ‐ +2.8 per mil with –3.1 ‐ +2.8 per mil for the stage 1 and –0.5 ‐ +2.1 for the stage 2, showing the isotopic characteristics of mantle derived sulfur. The δ13C values of vein dolomites vary from –5.3 to –7.2 per mil, with –5.3 ‐ –6.6 per mil for the stage 1 and –5.3 ‐ –7.2 per mil for the stage 2, which are significantly different from those of surrounding Triassic marble with δ13C values of –0.3 ‐ +2.8 per mil, and show characteristics of mantle derived carbon. The δ18O values of vein dolomites range from +10.2 to +13.1 per mil, which are higher than those of carbonatite, but lower than those of the marble. Their corresponding δ18Owater values are +0.6 ‐ +3.9 per mil, with +2.7 ‐ +3.8 per mil for the stage 1 and +0.6 ‐ +3.9 per mil for the stage 2. The data implies that these vein carbonates were formed by the mixing fluids of magmatic or mantle source with meteoric or formation water. The δ18O values of ore‐forming fluids responsible for the formation of vein quartz are estimated to be +3.2 to +6.8, the δD values of inclusion fluids of the quartz are measured to be –54 to –82 per mil. All those stable isotopic data suggest the involvement of the fluids from mantle and/or mantle‐derived magmas through fault system in the forming process of the Dashuigou tellurium deposit.  相似文献   

10.
Sulfur isotopic compositions were determined by ion microprobe for 36 spots on anhydrite crystals in trachyandesitic pumices erupted from El Chichón Volcano in 1982. Individual anhydrite crystals are homogeneous in δ34S, within the ±1‰ (2σ) uncertainty of the method, but crystal-to-crystal variations are large (+2.5 to +10.9‰). The mean δ34S for anhydrite (+6.4 ± 2.1‰, 1σ) is significantly lower than earlier results for bulk anhydrite separates (+9.0 to +9.2‰). The difference between the mean δ34S values in these two populations may reflect a grain-size effect, with heavier sulfur concentrated in smaller anhydrite crystals, few of which were analyzed by ion microprobe. Variations in δ34S show no correlation with complex textures in anhydrite revealed by cathodoluminescence color. Ion-microprobe analyses of δ34S were also obtained on six ovoid-shaped inclusions of pyrrhotite, chalcopyrite, and/or intermediate sulfide solid solution hosted by silicate or oxide crystals, interpreted to be magmatic (δ34S = −0.1 to +2.7‰; mean +0.7‰), and on four irregularly shaped multiphase sulfide fragments in the matrix, interpreted as xenocrystic, which range widely in δ34S (−3.7 to +5.5‰). We evaluate four different mixing scenarios involving (1) magmatic anhydrite and sedimentary sulfate, (2) magmatic anhydrite and hydrothermal anhydrite, and anhydrite and coexisting sulfide crystals precipitated in different domains of a common magma reservoir that were affected by (3) different degrees of degassing or (4) different degrees of crustal sulfur contamination. The model involving physical contamination of sedimentary sulfate is considered untenable. The other three models are considered to be viable, but none of them can explain all observations. The results of this study and other recent investigations prompt a re-evaluation of the sulfur budget for the 1982 El Chichón eruption. We estimate that 2.2 × 1013 g of S was emitted, and that 58 wt.% of the sulfur was present as anhydrite prior to eruption, with the remainder in a vapor phase, with H2S/SO2 ≈ 9. The bulk magmatic δ34S value for the 1982 El Chichón trachyandesite is estimated as +4.1 to +5.8‰, typical of the relatively heavy sulfur isotopic compositions that characterize subduction-related magmas.  相似文献   

11.
Five lizardite-chrysotile type serpentinites from California, Guatemala and the Dominican Republic show oxygen isotope fractionations of 15.1 to 12.9 per mil between coexisting serpentine and magnetite (O18 magnetite=–7.6 to –4.6 per mil relative to SMOW). Nine antigorites (mainly from Vermont and S. E. Pennsylvania) show distinctly smaller fractionations of 8.7 to 4.8 per mil (O18 magnetite=–2.6 to +1.7 per mil). Two lizardite and chrysotile serpentinites dredged from the Mid-Atlantic Ridge exhibit fractionations of 10.0 and 12.4 per mil (O18 magnetite=–6.8 and –7.9 per mil, respectively), whereas an oceanic antigorite shows a value of 8.2 per mil (O18 magnetite=–6.2). These data all clearly indicate that the antigorites formed at higher temperatures than the chrysotilelizardites. Electron microprobe analyses of magnetites from the above samples show that they are chemically homogeneous and essentially pure Fe3O2. However, some magnetites from certain other samples that show a wide variation of Cr content also give very erratic oxygen isotopic results, suggesting non-equilibrium. An approximate serpentine-magnetite geothermometer curve was constructed by (1) extrapolation of observed O18 fractionations between coexisting chlorites and Fe-Ti oxides in low-grade pelitic schists whose isotopic temperatures are known from the quartz-muscovite O18 geothermometer, and (2) estimates of the O18 fractionation factor between chlorite and serpentine (assumed to be equal to unity). This serpentine-magnetite geothermometer suggests approximate equilibrium temperatures as follows: continental lizardite-chrysotile, 85° to 115° C; oceanic lizardite and chrysotile, 130° C and 185° C, respectively; oceanic antigorite, 235° C; and continental antigorites, 220° to 460° C.Contribution No. 2029 of the Division of Geological and Planetary Sciences, California Institute of Technology, Pasadena, California 91109.  相似文献   

12.
The Quesnel River gold deposit (1.2 million tonnes grading 5.22 g/t Au in three separate zones) occurs within Takla Group volcanic rocks of Upper Triassic age proximal to an alkalic stock. The deposit occurs in amphibole-augite phyric, fragmental, basaltic rocks. Alteration has produced an assemblage of epidote-chloritetremolite-calcite-quartz with lesser pyrite, chalcopyrite, pyrrhotite, sphalerite, marcasite, galena, arsenopyrite and gold.The West Zone comprises a tabular, conformable sulfide body underlain by bedded, variably altered fragmental basaltic rocks and overlain by siltstone and argillite. In the Main Zone, highest gold grades occur adjacent to a sharp discordant alteration front with barren, strongly carbonatized, pyritic basaltic lapilli-tuff. It is overlain by siltstone and argillite and bounded to the east and a depth by a west dipping reverse fault. To the west the auriferous, propylitically altered, rocks grade laterally into lower grade and barren basaltic rocks.Oxygen(18O = + 9 to + 15) and carbon (13O= -14 to –7) isotopic signatures of calcite from carbonate-altered and propylitically altered rocks are similar. However, sulfur isotopic values for pyrite are different, with gold-associated pyrite (34S = –7 to –3) distinct from pyrite in carbonate altered rocks with (34S = + 8 to + 13).The carbonization occurred before complete induration of the basaltic fragmental rocks, whereas propylitization and gold plus sulfide precipitation is clearly epigenetic.  相似文献   

13.
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   

14.
Stibnite mineralisation in the antimony province of New England can be divided into Central type ores (veins of stibnite + quartz ± berthierite) and Peripheral type ores of stibnite + quartz + native antimony ± berthierite. The Central stibnites have 34SCDT values of –5±2 (1) which may represent equilibrium precipitation from mantle sulfur at about 200°C. Peripheral stibnites have 34S values between 0 and –25, with a large group at 0±2. They represent precipitation from a limited supply of mantle sulfur and the acquisition of sedimentary sulfur. We consider that the different ore types were produced from distinct ore solutions derived from two immiscible melts. These originated in the deep mantle, were mobilised by tectonic activity and supplied the antimony and most of the sulfur to the ores.  相似文献   

15.
The Wolyu mine is one of the largest vein-type gold-silver-bearing epithermal systems in the Youngdong district and is the first gold-silver deposit in Korea found to contain significant germanium, in the form of argyrodite (Ag8GeS6). Mineralized veins (78.9 ± 1.2 Ma) crosscutting Late Cretaceous hostrock tuff and quartz porphyry (81.5 ± 1.8 Ma) consist of three stages of quartz and carbonates, the first of which contains pyrite, basemetal sulfides and Au-Ag-minerals. Stage I Au-Ag-Ge-mineralized veins show a systematic variation of mineral assemblage with time: (1) quartz + pyrite; (2) quartz + pyrite + sphalerite + electrum + argentite; (3) carbonate + quartz + sphalerite + electrum + argentite; (4) carbonate + native silver + argentite + Ag-sulfosalts + argyrodite + sphalerite. Calculated values of temperature and sulfur activity are: assemblage (1), 360-280°C and 10–7-10–10; (2), 280-210°C and 10–10-10–14; (3), 210-180°C and 10–14-10–16; (4), 180-155°C and 10–17-10–18. These data, the frequent association of gold with sulfides, and the abundance of pyrite in alteration zones indicate that decreasing sulfur activity and cooling were important in triggering gold deposition. Hydrogen and oxygen isotope compositions of ore fluids display a systematic variation with increasing time. Within the main Ag-Au-Ge mineralization, D and 18O values decrease with the transition from quartz to carbonate deposition (from -78 and –2.8% to –90 and –8.7%., respectively), indicating increasing involvement (mixing) of less evolved meteoric water which resulted in progressive cooling and dilution of ore fluids in the shallow ( 370–600 m) Wolyu epithermal system.  相似文献   

16.
Previous studies of galena and sphalerite from Paleozoic MVT deposits in the Viburnum Trend, southeast Missouri documented large variations in 34S values throughout the ore-forming event. The present study of Cu-Fe-sulfides reveals a similar 34S variation that reflects two end-member sulfur reservoirs whose relative importance varied both temporally and spatially. More 34S-enriched sulfides (34S approaching 25) indicate introduction of sulfur from basinal sedimentary sources, whereas more 32S-enriched sulfides (34S < 5) may reflect fluids moving through underlying granitic basement. Two areas containing Precambrian, igneous-hosted FeCu mineralization in southeast Missouri (West and Central Domes of Boss-Bixby) were investigated to elucidate their relationship to Cu-rich MVT orebodies hosted nearby within the overlying Cambrian Bonneterre Dolomite. Mineralization at Boss-Bixby is composed of an early phase of iron oxide deposition followed by Cu-Fe-sulfides. The Central Dome is faulted and its mineralization is more fracture-controlled than the typically podiform ores of the West Dome. The 34S values of West Dome sulfides are 0.9 to 6.5 and pyrite-chalcopyrite indicate a temperature of 525° ± 50 °C. These data indicate an igneous source of sulfur during Precambrian ore deposition. In contrast, 34S values of Central Dome sulfides are 9.4 to 20.0 and pyrite-chalcopyrite indicate temperatures of 275° ± 50 °C. Similar 34S values are obtained for chalcopyrite from the overlying MVT deposits. We speculate that deeply circulating, basin-derived MVT fluids mobilized sulfur and copper from the underlying igneous basement and redeposited them in overlying Curich MVT orebodies, as well as overprinting earlier Precambrian sulfides of the Central Dome with a later, Paleozoic MVT sulfur isotope signature. Many models for MVT fluid circulation in the Midcontinent region of North America assume that igneous basement rocks are an impermeable boundary, but in southeast Missouri, evidence exists for structurally controlled MVT fluid movement > 600 m vertically through underlying Precambrian igneous rocks. Such basement involvement has been suggested for other carbonate-hosted base-metal districts (e.g. Irish base metal deposits) and should be considered an integral part of the ore-forming process in southeast Missouri.  相似文献   

17.
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   

18.
The Myall Creek copper prospect is in unmetamorphosed carbonaceous dolosiltstone and sandstone at the base of the late Proterozoic (Adelaidean) Tapley Hill Formation. It contains disseminated, fine-grained chalcopyrite, zincian tennanite, bornite, chalcocite, pyrite, sphalerite and galena, and irregular to straight chalcopyrite-rich veinlets. Some ore minerals rim and/or partially replace pyrite or clastic grains. There is no evidence of hydrothermal activity. The 34SCDT values of pyrite and the other sulfides fall in the wide range –3.6 to +44.2. Dolomite in both mineralised and unmineralised samples has 13CPDB values concentrated around –3, and 18OSMOW values around +25. It is concluded that the mineralising fluids were near-neutral brines which leached metals from the basement and early Adelaidean rocks. They entered the Tapley Hill sediments at moderately low temperatures via permeable strata and faults. The metals were precipitated by biogenic H2S, and also fixed by reaction with iron sulfides and, possibly, organic matter. Continuing ascent of brines into the mineralised strata caused breakdown of detrital feldspars and Fe-Ti oxides, and some solution-remobilisation of early-formed sulfides.  相似文献   

19.
Mantle-derived peridotite bodies of Ariège are composed of spinel lherzolites and harzburgites ranging from remarkably fresh (less than 5% serpentinized) samples with protogranular texture to secondary foliated samples, which are generally 10%–20% serpentinized. The foliated samples have passed through two cycles of deformation and re-crystallization, the earlier ones occurring at temperatures above 950° C for 15 kbar pressure, the later ones at temperatures between 950° and 750° C for 8–15 kbar. Microscopic investigation of 140 samples reveals an accessoy sulfide component which is more abundant in lherzolie than in harzburgite. This component occurs in two differet textural locations, either as inclusions trapped within silicates during the first stage of re-crystallization or as interstitial grains among silicates. Mineralogy and chemistry of both sulfide occurrences are quite similar, at least in samples less than 5% serpentinized. In these fresh samples, sulfides are composed of complex intergrowths between nickel-rich pentlandite and pyrite, coexisting with minor primary pyrrhotite (Fe7S8) and chalcopyrite. Pentlandite and pyrite are interpreted as low-temperature breakdown products of upper mantle monosulfide solid solutions. The mineralogy and chemistry of interstitial sulfides in serpentinized rocks vary in parallel with the degree of serpentinization. In samples less than 10% serpentinized, primary pyrrhotite grades into FeS. In samples more than 10% serpentinized, pyrite is replaced by secondary pyrrhotite, and then disappears totally, whereas the coexisting pentlandite is Fe-enriched and replaced by mackinawite. This sequence of alteration indicates a decrease of sulfur fugacity, resulting from serpentinization of olivine at temperatures below 300° C. This is also the case for the inclusions which have been fractured during the tectonic emplacement of the host peridotites within the crust. The presence of non-equilibrium sulfide assemblages in both cases reflects the sluggishness of solid state reactions at near-surface temperatures. It is inferred from these results that sulfides disseminated within orogenic peridotite massifs are so sensitive to serpentinization that most sulfur fugacity estimates based on fractured inclusions and intergranular sulfides are unreliable.  相似文献   

20.
The several-hundred-m-thick Miocene Upper Red Formation in northwestern Iran hosts stratiform and fault-controlled copper mineralization. Copper enrichment in the percent range occurs in dm-thick carbonaceous sandstone and shale units within the clastic redbed sequence and consists of fine-grained disseminated copper sulfides (chalcopyrite, bornite, chalcocite) and supergene alteration minerals (covellite, malachite and azurite). The copper mineralization formed after calcite cementation of the primary rock permeability. Copper sulfides occur mainly as replacement of diagenetic pyrite, which, in turn, replaced organic matter. Electron microprobe analysis on bornite, chalcocite and covellite identifies elevated silver contents in these minerals (up to 0.12, 0.72 and 1.21 wt%, respectively), whereas chalcopyrite and pyrite have only trace amounts of silver (<0.26 and 0.06 wt%, respectively). Microthermometric data on fluid inclusions in authigenic quartz and calcite indicate that the Cu mineralization is related to a diagenetic fluid of moderate-to low temperature (Th = 96–160 °C) but high salinity (25–38 wt% CaCl2 equiv.). The range of δ34S in pyrite is −41.9 to −16.4‰ (average −31.4‰), where framboidal pyrite shows the most negative values between −41.9 and −31.8‰, and fine-grained pyrite has relatively heavier δ34S values (−29.2 to −16.4‰), consistent with a bacteriogenic derivation of the sulfur. The Cu-sulfides (chalcopyrite, bornite and chalcocite) show slightly heavier values from −14.6 to −9.0‰, and their sulfur sources may be both the precursor pyrite-S and the bacterial reduction of sulfate-bearing basinal brines. Carbonates related to the ore stage show isotopically light values of δ13CV-PDB from −8.2 to −5.1‰ and δ18OV-PDB from −10.3 to −7.2‰, indicating a mixed source of oxidation of organic carbon (ca. −20‰) and HCO3− from seawater/porewater (ca. 0‰). The copper mineralization is mainly controlled by organic matter content and paleopermeability (intragranular space to large fracture patterns), enhanced by feldspar and calcite dissolution. The Cheshmeh-Konan deposit can be classified as a redbed-type sediment-hosted stratiform copper (SSC) deposit.  相似文献   

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