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1.
The Southern Great Xing'an Range(S(GXR)which forms part of the eastern segment of the Central Asian Orogenic Belt(CAOB)is known as one of the most important Cu-Mo-Pb-Zn-Ag-Au metallogenic belts in China,hosting a number of porphyry Mo(Cu),skarn Fe(Sn),epithermal Au-Ag,and hydrothermal veintype Ag-Pb-Zn ore deposits.Here we investigate the Bianjiadayuan hydrothermal vein-type Ag-Pb-Zn ore deposit in the southern part of the SGXR.Porphyry Sn± Cu± Mo mineralization is also developed to the west of the Ag-Pb-Zn veins in the ore field.We identify a five-stage mineralization process based on field and petrologic studies including(i)the early porphyry mineralization stage,(ii)main porphyry mineralization stage,(iii)transition mineralization stage,(iv)vein-type mineralization stage and(v)late mineralization stage.Pyrite is the predominant sulfide mineral in all stages except in the late mineralization stage,and we identify corresponding four types of pyrites:Pyl is medium-grained subhedral to euhedral occurring in the early barren quartz vein;Py2 is medium-to fine-grained euhedral pyrite mainly coexisting with molybdenite,chalcopyrite,minor sphalerite and galena;Py3 is fine-grained,subhedral to irregular pyrite and displays cataclastic textures with micro-fractures;Py4 occurs as euhedral microcrystals and forms irregularly shaped aggregate with sphalerite and galena.LA-ICP-MS trace element analyses of pyrite show that Cu,Pb,Zn,Ag,Sn,Cd and Sb are partitioned into pyrite as structurally bound metals or mineral micro/nano-inclusions,whereas Co,Ni,As and Se enter the lattice via isomorphism in all types of pyrite.The Cu,Zn,Ag,Cd concentrations gradually increase from Pyl to Py4,which we correlate with cooling and mixing of ore-forming fluid with meteoric water.Py2 contains the highest contents of Co,Ni,Se,Te and Bi,suggesting high temperature conditions for the porphyry mineralization stage.Ratios of Co/Ni(0.03-10.79,average 2.13)and sulphur isotope composition of sulfide indicate typical hydrothermal origin for pyrites.The δ~(34)S_(cDT) values of Pyl(0.42‰-1.61‰,average1.16‰),Py2(-1.23‰to 0.82‰,average 0.35‰),Py3(—0.36‰to 2.47‰average 0.97‰).Py4(2.51‰--3.72‰,average 3.06‰),and other sulfides are consistent with those of typical porphyry deposit(-5‰to 5‰),indicating that the Pb-Zn polymetallic mineralization in the Bianjiadayuan deposit is genetically linked to the Yanshanian(Jurassic-Cretaceous)magmatic-hydrothermal events.Variations of δ~(34) S values are ascribed to the changes in physical and chemical conditions during the evolution and migration of the ore-forming fluid.We propose that the high Sn content of pyrite in the Bianjiadayuan hydrothermal vein-type Pb-Zn polymetallic deposit can be used as a possible pathfinder to prospect for Sn mineralization in the surrounding area or deeper level of the ore field in this region.  相似文献   

2.
The sulfur isotopic composition of carbonate associated sulfate (CAS) has been used to investigate the geochemistry of ancient seawater sulfate. However, few studies have quantified the reliability of δ34S of CAS as a seawater sulfate proxy, especially with respect to later diagenetic overprinting. Pyrite, which typically has depleted δ34S values due to authigenic fractionation associated with bacterial sulfate reduction, is a common constituent of marine sedimentary rocks. The oxidation of pyrite, whether during diagenesis or sample preparation, could thus adversely influence the sulfur isotopic composition of CAS. Here, we report the results of CAS extractions using HCl and acetic acid with samples spiked with varying amounts of pyrite. The results show a very strong linear relationship between the abundance of fine-grained pyrite added to the sample and the resultant abundance and δ34S value of CAS. This data represents the first unequivocal evidence that pyrite is oxidized during the CAS extraction process. Our mixing models indicate that in samples with much less than 1 wt.% pyrite and relatively high δ34Spyrite values, the isotopic offset imparted by oxidation of pyrite should be much less than ? 4‰. A wealth of literature exists on the oxidation of pyrite by Fe3+ and we believe this mechanism drives the oxidation of pyrite during CAS extraction, during which the oxygen used to form sulfate is taken from H2O, not O2. Consequently, extracting CAS under anaerobic conditions would only slow, but not halt, the oxidation of pyrite. Future studies of CAS should attempt to quantify pyrite abundance and isotopic composition.  相似文献   

3.
《地学前缘(英文版)》2020,11(4):1369-1380
This paper reports new geochronological (U–Pb) and isotope (C, O, and S) data to investigate the timing of mineralization and mode of ore genesis for the recently discovered Changtuxili Mn–Ag–Pb–Zn deposit, located on the western slopes of the southern Great Hinggan Range in NE China. The mineralization is hosted by intermediate–acidic lavas and pyroclastic rocks of the Baiyingaolao Formation. Three stages of mineralization are identified: quartz–pyrite (Stage I), galena–sphalerite–tetrahedrite–rhodochrosite (Stage II), and quartz–pyrite (Stage III). δ13C and δ18O values for carbonate from the ore vary from −8.51‰ to −4.96‰ and 3.97‰ to 15.90‰, respectively, which are indicative of a low-temperature alteration environment. δ34SV-CDT values of sulfides range from −1.77‰ to 4.16‰ and show a trend of equilibrium fractionation (δ34SPy ​> ​δ34SSp ​> ​δ34SGn). These features indicate that pyrite, sphalerite, and galena precipitated during the period of mineralization. The alteration mineral assemblage and isotope data indicate that the weakly acidic to weakly alkaline ore-forming fluid was derived largely from meteoric water and the ore-forming elements C and S originated from magma. During the mineralization, a geochemical barrier was formed by changes in the pH of the ore-forming fluid, leading to the precipitation of rhodochrosite. On the basis of the mineralization characteristics, new isotope data, and comparison with adjacent deposits, we propose that the Changtuxili Mn–Ag–Pb–Zn deposit is an intermediate-to low-sulfidation epithermal deposit whose formation was controlled by fractures and variability in the pH of the ore-forming fluid. The surrounding volcanic rocks yield zircon U–Pb ages of 160−146 ​Ma (Late Jurassic), indicating that the mineralization is younger than 146 ​Ma.  相似文献   

4.
Pb–Zn deposits are widespread and common in various parts of the Taurus Belt. Most of the deposits are of pyrometasomatic and hydrothermal origin. The Keban Pb–Zn deposits are located along the intrusive contact between the Paleozoic – Lower Triassic Keban Metamorphic Formation and the syenite porphyry of the Upper Cretaceous Keban igneous rocks. Various studies have already been carried out; using fluid inclusion studies on fluorite, calcite and quartz on the pyrite–chalcopyrite bearing Keban ore deposits. This study focuses on the interpretation of stable isotope compositions in connexion with fluid inclusion data. Sulphur isotope values (δ34S) of pyrite are within the range of ?0.59 to +0.17‰V-CDT (n = 10). Thus, the source of sulphur is considered to be magmatic, as evidenced by associated igneous rocks and δ34S values around zero“0”. Oxygen isotope values δ18O of quartz vary between +10.5 and +19.9‰(SMOW). However, δ18O and δ13C values of calcite related to re-crystallized limestone (Keban Metamorphic Formation) reach up to +27.3‰(SMOW) and +1.6‰(PDB), respectively. The δ34S, δ13C and δ18O values demonstrate that skarn-type Pb–Zn deposits formed within syeno-monzonitic rocks and calc-schist contacts could have developed at low temperatures, by mixing metamorphic and meteoric waters in the final stages of magmatism.  相似文献   

5.

The stable enrichment of pyrite from magnesite ores in δ34S isotope (from 5.4 to 6.9‰) compared with pyrite from the host (sedimentary and igneous) rocks was established in the classical Satka sparry magnesite ore field. Concretionary segregations of fine-grained pyrite in dolomite are depleted in the heavy sulfur isotope (δ34S, from–9.1 to–5.8‰). Pyrite from dolerite is characterized by δ34S values (–1.1 and 1.7‰) close to the meteorite sulfur. The δ34S values in barite from the underlying dolomite horizon vary in the range of 32.3–41.4‰. The high degree of homogeneity of the sulfur isotope composition in pyrite from magnesite is a result of thermochemical sulfate reduction during the syngenetic crystallization of pyrite and magnesite from epigenetic brines, formed during dissolution of evaporite sulfate minerals at the stage of early catagenesis of the Riphean deposits.

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6.
The extensive Changba-Lijiagou Pb-Zn deposit is located in the north of the Xihe–Chengxian ore cluster in West Qinling. The ore bodies are mainly hosted in the marble, dolomitic marble and biotite-calcite-quartz schist of the Middle Devonian Anjiacha Formation, and are structurally controlled by the fault and anticline. The ore-forming process can be divided into three main stages, based on field geological features and mineral assemblages. The mineral assemblages of hydrothermal stage I are pale-yellow coarse grain, low Fe sphalerite, pyrite with pits, barite and biotite. The mineral assemblages of hydrothermal stage II are black-brown cryptocrystalline, high Fe shalerite, pyrite without pits, marcasite or arsenopyrite replace the pyrite with pits, K-feldspar. The features of hydrothermal stage III are calcite-quartz-sulfide vein cutting the laminated, banded ore body. Forty-two sulfur isotope analyses, twenty-five lead isotope analyses and nineteen carbon and oxygen isotope analyses were determined on sphalerite, pyrite, galena and calcite. The δ34 S values of stage I(20.3 to 29.0‰) are consistent with the δ34 S of sulfate(barite) in the stratum. Combined with geological feature, inclusion characteristics and EPMA data, we propose that TSR has played a key role in the formation of the sulfides in stage I. The δ34 S values of stage II sphalerite and pyrite(15.1 to 23.0‰) are between sulfides in the host rock, magmatic sulfur and the sulfate(barite) in the stratum. This result suggests that multiple S reservoirs were the sources for S2-in stage II. The δ34 S values of stage III(13.1 to 22‰) combined with the structure of the geological and mineral features suggest a magmatic hydrothermal origin of the mineralization. The lead isotope compositions of the sulfides have 206 Pb/204 Pb ranging from 17.9480 to 17.9782, 207 Pb/204 Pb ranging from 15.611 to 15.622, and 208 Pb/204 Pb ranging from 38.1368 to 38.1691 in the three ore-forming stages. The narrow and symmetric distributions of the lead isotope values reflect homogenization of granite and mantle sources before the Pb-Zn mineralization. The δ13 CPDB and δ18 OSMOW values of stage I range from-0.1 to 2.4‰ and from 18.8 to 21.7‰. The values and inclusion data indicate that the source of fluids in stage I was the dissolution of marine carbonate. The δ13 CPDB and δ18 OSMOW values of stage II range from-4 to 1‰ and from 12.3 to 20.3‰, suggesting multiple C-O reservoirs in the Changba deposit and the addition of mantle-source fluid to the system. The values in stage III are-3.1‰ and 19.7‰, respectively. We infer that the process of mineralization involved evaporitic salt and sedimentary organic-bearing units interacting through thermochemical sulfate reduction through the isotopic, mineralogy and inclusion evidences. Subsequently, the geology feature, mineral assemblages, EPMA data and isotopic values support the conclusion that the ore-forming hydrothermal fluids were mixed with magmatic hydrothermal fluids and forming the massive dark sphalerite, then yielding the calcite-quartz-sulfide vein ore type at the last stage. The genesis of this ore deposit was epigenetic rather than the previously-proposed sedimentary-exhalative(SEDEX) type.  相似文献   

7.
The reported source rocks for the abundant petroleum in the Tarim Basin, China range from Cambrian to Lower Ordovician and/or Upper Ordovician in age. However, the difference between the two groups of source rocks is not well characterized. In this study, pyrite was removed from eleven mature to over mature kerogen samples from source rocks using the method of CrCl2 reduction and grinding. The kerogen and coexisting pyrite samples were then analyzed for δ34S values. Results show that the kerogen samples from the Cambrian have δ34S values between +10.4‰ and +19.4‰. The values are significantly higher than those from the Lower Ordovician kerogen (δ34S of between +6.7‰ and +8.7‰), which in turn are generally higher than from the Upper Ordovician kerogen samples (δ34S of between ?15.3 and +6.8‰). The associated pyrite shows a similar trend but with much lower δ34S values. This stratigraphically controlled sulfur isotope variation parallels the evolving contemporary marine sulfate and dated oil δ34S values from other basins, suggesting that seawater sulfate and source rock age have an important influence on kerogen and pyrite δ34S values. The relatively high δ34S values in the Cambrian to Lower Ordovician source rocks are associated with abundant aryl isoprenoids, gammacerane and C35 homohopanes in the extractable organic matter, indicating that these source rocks were deposited in a bottom water euxinic environment with water stratification. Compared with the Upper Ordovician, the Cambrian to Lower Ordovician source rocks show abundance in C28 20R sterane, C23 tricyclic terpanes, 4,23,24-trimethyl triaromatic dinosteroids and depletion in C24 tetracyclic terpane, C29 hopane. Thus, δ34S values and biomarkers of source rock organic matter can be used for distinguishing the Cambrian and Upper Ordovician source rocks in the Tarim Basin.  相似文献   

8.
Massive Zn‐Pb‐Ag sulfide mineralization appears conformable with felsic volcanism, developed in an Upper Jurassic volcanic arc to the Southwest (SW) of the Serbo‐Macedonian continent in Northern Greece. The host volcanic sequence of the mineralization comprises mylonitized rhyolitic to rhyodacitic lavas, pyroclastics, quartz‐feldspar porphyries, and cherty tuffs. A “white mica—quartz—pyrite” mineral assemblage characterizes the volcanic rocks in the footwall and hanging‐wall of massive sulfide ore layers, formed as a result of greenschist‐grade regional metamorphism on “clay‐quartz‐pyrite” hydrothermal alteration haloes. Massive ore lenses are usually underlain by deformed Cu‐pyrite and quartz‐pyrite stockworks. Most of the sulfide ore bodies have proximal‐type features. Ductile deformation and regional metamorphism have transformed many of the stockwork structures. The mineralization is characterized by high Zn, Pb, and Ag contents, while Cu and critical metals are low. Primary depositional textures, for example, layering, clastic pyrite, colloform, and atoll textures were identified. The overall textural features of the mineralization indicate it has undergone mechanical deformation. The most prominent features of the effects of metamorphism, folding and shearing, are modification of the ore body morphology toward flattened and boudinage structures and transformation of the ore textures toward the dominance of planar fabrics. Sulfur isotope analyses of sulfides along with textural observations are consistent with a dual source of sulfide sulfur. Sulfur isotope values for sphalerite, non‐colloform pyrite, galena, and chalcopyrite fall in a limited range from ?1.6 to +4.8‰ (mean δ34S + 2‰), indicating a hydrothermal source derived from the reduction of coeval seawater sulfate in the convective system. Pyrites with colloform and atoll textures are characterized by a 34S depletion, indicating a bacterial reduction of coeval seawater sulfate. The morphology of ore beds, the mineralogy, sulfide textures, and ore chemistry along with the petrology and tectonic setting of the host rocks can be attributed to typical of a bimodal‐felsic metallogenesis. Although similar in many respects to classic Kuroko‐type volcanogenic massive sulfide mineralization, it has some atypical features, like the absence of barite ore, which is possibly a result of significant temporal depletion in sulfate due to bacterial reduction, a conclusion supported by the widespread occurrence of colloidal and atoll textures of pyrite.  相似文献   

9.
Sulfur isotopic disequilibrium is commonly observed between associated pyrite and copper sulfides in NW Queensland. A sulfur isotopic study of copper mineralization in dolomites at Paradise Valley and arenites at Mammoth has allowed the significance of such disequilibrium to be evaluated. Copper mineralization at Paradise Valley is characterized by a greater enrichment in 34S, with δ34S values often greater than +30‰, for both copper sulfides and associated syngenetic/diagneetic pyrite. At Mammoth, copper sulfides have isotopic compositions (δ34S=?15.9 to ?0.3‰) transitional between disseminated syngenetic/diagenetic pyrite (δ34S=?5.7 to ?1.7‰) and epigenetic vein pyrite (δ34S=?17.9 to ?7.1‰) suggesting progressive reaction and replacement of syngenetic/diagenetic pyrite by a copper-bearing mineralizing fluid under oxidizing conditions. The isotopic data, within the constraints imposed by geological and geochemical factors, support a model of reaction between copper-bearing mineralizing fluids and pre-existing syngenetic/diagenetic pyrite for both the carbonate- and arenite-hosted deposits.  相似文献   

10.
The carbonate-hosted Pb–Zn deposits in the Sanjiang metallogenic belt on the Tibetan Plateau are typical of MVT Pb–Zn deposits that form in thrust-fold belts. The Jiamoshan Pb–Zn deposit is located in the Changdu area in the middle part of the Sanjiang belt, and it represents a new style of MVT deposit that was controlled by karst structures in a thrust–fold system. Such a karst-controlled MVT Pb–Zn deposit in thrust settings has not previously been described in detail, and we therefore mapped the geology of the deposit and undertook a detailed study of its genesis. The karst structures that host the Jiamoshan deposit were formed in Triassic limestones along secondary reverse faults, and the orebodies have irregular tubular shapes. The main sulfide minerals are galena, sphalerite, and pyrite that occur in massive and lamellar form. The ore-forming fluids belonged to a Mg2+–Na+–K+–SO2-4–Cl-–F-–NO-3–H2 O system at low temperatures(120–130°C) but with high salinities(19–22% NaCl eq.). We have recognized basinal brine as the source of the ore-forming fluids on the basis of their H–O isotopic compositions(-145‰ to-93‰ for δDV-SMOW and-2.22‰ to 13.00‰ for δ18 Ofluid), the ratios of Cl/Br(14–1196) and Na/Br(16–586) in the hydrothermal fluids, and the C–O isotopic compositions of calcite(-5.0‰ to 3.7‰ for δ13 CV-PDB and 15.1‰ to 22.3‰ for δ18 OV-SMOW). These fluids may have been derived from evaporated seawater trapped in marine strata at depth or from Paleogene–Neogene basins on the surface. The δ34 S values are low in the galena(-3.2‰ to 0.6‰) but high in the barite(27.1‰), indicating that the reduced sulfur came from gypsum in the regional Cenozoic basins and from sulfates in trapped paleo-seawater by bacterial sulfate reduction. The Pb isotopic compositions of the galena samples(18.3270–18.3482 for 206 Pb/204 Pb, 15.6345–15.6390 for 207 Pb/204 Pb, and 38.5503–38.5582 for 208 Pb/204 Pb) are similar to those of the regional Triassic volcanic-arc rocks that formed during the closure of the Paleo-Tethys, indicating these arc rocks were the source of the metals in the deposit. Taking into account our new observations and data, as well as regional Pb–Zn metallogenic processes, we present here a new model for MVT deposits controlled by karst structures in thrust–fold systems.  相似文献   

11.
The large tonnage Maoling gold deposit (25 t @ 3.2 g/t) is located in the southwest Liaodong Peninsula, North China Craton. The deposit is hosted in the Paleoproterozoic metamorphic rocks. Four stages of mineralization were identified in the deposit: (stage I) quartz-arsenopyrite ± pyrite, (stage II) quartz-gold- arsenopyrite-pyrrhotite, (stage III) quartz-gold- polymetallic sulfide, and (stage IV) quartz-calcite-pyrrhotite. In this paper, we present fluid inclusion, C-H-O-S-Pb-He-Ar isotope data, zircon U-Pb, and gold-bearing sulfide (i.e. arsenopyrite and pyrrhotite) Rb-Sr age of the Maoling gold deposit to constrain its genesis and ore-forming mechanism. Three types of fluid inclusions were distinguished in quartz-bearing veins, including liquid-rich two-phase (WL type), gas-rich two-phase (GL type), and daughter mineral-bearing fluid inclusions (S type). Fluid inclusions data show that the homogenization at temperatures 197 to 372 °C for stage I, 126 to 319 °C for stage II, 119 to 189 °C for stage III, and 115 to 183 °C for stage IV, with corresponding salinities of 3.7 to 22.6 wt.%, 4.7 to 23.2 wt.%, 5.3 to 23.2 wt.%, and 1.7 to 14.9 wt.% NaCl equiv., respectively. Fluid boiling was the critical factor controlling the gold and associated sulfide precipitation at Maoling. Hydrogen and oxygen stable isotopic analyses for quartz yielded δ18O = ?5.0‰ to 9.8‰ and δ D = ?133.5‰ to ?77.0‰. Carbon stable isotopic analyses for calcite and ankerite yielded δ13C = ?2.3‰ to ?1.2‰ and O = 7.9‰ to 14.1‰. The C-H-O isotope data show that the ore-forming fluids were originated from magmatic water with meteoric water input during mineralization. Hydrothermal inclusions in arsenopyrite have 3He/4He ratios of 0.002 Ra to 0.054 Ra, and 40Ar/36Ar rations of 1225 to 3930, indicating that the ore-forming fluids were dominantly derived from crustal sources almost no mantle input. Sulfur isotopic values of Maoling fine-grained granite range from 6.‰1 to 9.8‰, with a mean of 7.7‰, δ34S values of arsenopyrite from the mineralized phyllite (host rock) range from 8.9‰ to 10.6‰, with a mean of 10.0‰, by contrast, δ34S values of sulfides from ore vary between 4.3‰ and 10.6‰, with a mean of 6.8‰, suggesting that sulfur was mainly originated from both the host rock and magma. Lead radioactive isotopic analyses for sulfides yielded 206Pb/204Pb = 15.830–17.103, 207Pb/204Pb = 13.397–15.548, 208Pb/204Pb = 35.478–36.683, and for Maoling fine-grained granite yielded 206Pb/204Pb = 18.757–19.053, 207Pb/204Pb = 15.596–15.612, and 208Pb/204Pb = 38.184–39.309, also suggesting that the ore-forming materials were mainly originated from the host rocks and magma. Zircon U-Pb dating demonstrates that the Maoling fine-grained granite was emplaced at 192.7 ± 1.8 Ma, and the host rock (mineralized phyllite) was emplaced at some time after 2065.0 ± 27.0 Ma. Arsenopyrite and pyrrhotite give Rb–Sr isochron age of 188.7 ± 4.5 Ma, indicating that both magmatism and mineralization occurred during the Early Jurassic. Geochronological and geochemical data, together with the regional geological history, indicate that Early Jurassic magmatism and mineralization of the Maoling gold deposit occurred during the subducting Paleo-Pacific Plate beneath Eurasia, and the Maoling gold deposit is of the intrusion-related gold deposit type.  相似文献   

12.
The Xinqiao Cu-S-Fe deposit in the Tongling ore district, Middle-Lower Yangtze River Valley Metallogenic Belt (MLYB; Eastern China), is located along the northern margin of the Yangtze Craton. The stratiform- and skarn-type Xinqiao mineralization comprises five stages, namely the early skarn (Stage I, garnet and diopside), late skarn (Stage II, epidote-dominated), iron oxides (Stage III, hematite and magnetite), colloform pyrite (Stage IV) and quartz-sulfides (Stage V). There are three pyrite types at Xinqiao, i.e., colloform (Py1; Stage IV), fine-grained (Py2, from Py1 recrystallization; Stage V) and coarse-grained (Py3; Stage V) pyrites.Scanning Electron Microscope (SEM) imagery for Py1 reveals that they are cubic microcrystalline pyrite aggregates, and the EDS and XRD data indicate that some Py1 contain minor siderite impurities. Electron Microprobe Analysis (EMPA) and LA-ICP-MS geochemical data demonstrate that the three pyrite types have relatively high Fe/S ratios and distinctly high Mn, Cu and As concentrations. Compared to Py2 and Py3, Py1 has higher Pb, Bi and Ag, but lower Co, Ni, Se, Cd, Te and Au. Ratios of Fe/S (0.837 to 0.906), Se/Te (2.39 to 14.50) and Co/Ni (0.67 to 4.67) of the Xinqiao pyrites resemble typical hydrothermal pyrites. δ34SCDT of Py1 (− 0.6‰ to 2.7‰, average 0.58‰), Py2 (1.8‰ to 2.5‰, average 2.1‰) and Py3 (1.9‰ to 4.4‰, average 3.5‰) are close to those of the Xinqiao skarn-type orebodies (1.3‰ to 4.1‰), but distinct from those of the Upper Carboniferous Huanglong Formation limestone (− 9.5‰ to − 15.4‰), suggesting that the three pyrite types (especially Py1) were genetically linked to the Yanshanian (Jurassic-Cretaceous) magmatic-hydrothermal events, with Py1 probably reflecting rapid crystallization during fluid mixing. We interpret that the Xinqiao stratiform mineralization may have been associated with the Jitou quartz diorite stock, as may be the case also for the skarn-type mineralization hosted in the contact between the Yanshanian Jitou stock and the Lower Permian Qixia Formation limestone. Overall, the Xinqiao Cu-S-Fe mineralization may have been generated by the Jurassic-Cretaceous tectono-thermal event in Eastern China.  相似文献   

13.
The S-isotope composition (δ34SCDT) of 213 samples of sulfides, sulfates and native sulfur from the pyrite mineralizations of southern Tuscany and associated country rocks were determined. The sulfur isotopic composition of pyrite is quite homogeneous and similar for all studied ore bodies, with an average δ34S value near +9,5‰. Pyrite disseminated within the Filladi di Boccheggiano formation, and thought to be authigenic, shows a much larger range of δ34S values (-13.1 to +14.5‰). The isotopic compositions of other sulfides associated with pyrite in the deposits show that isotopic equilibrium among sulfides was approached on a regional scale, but seldom fully attained. Isotopic data suggest that sedimentary marine sulfate was the ultimate source of sulfur in ores. Sulfates (mostly anhydrite) from the sulfate-carbonate lenses associated with both the Filladi di Boccheggiano and the Calcare Cavernoso formations also have similar and homogeneous compositions (average δ34S=+15–16‰). Coexisting sulfates and sulfides are not in isotopic equilibrium. In the light of the isotopic data, among the many proposed genetic models for the largest stratabound pyrite bodies the two following alternatives appear the most likely: 1) in agreement with recently suggested hypotheses, the ore bodies are older than the emplacement of the Mio-Pliocenic granitoids in the area, and are probably hydrothermal-sedimentary in origin, coeval with associated country rocks; 2) the ore bodies were formed as a consequence of bacterial reduction of anhydrite in low-temperature convection systems related to the early stages of the Mio-Pliocenic thermal anomaly. In both cases, the emplacement of the Mio-Pliocenic granitoids caused metamorphism and remobilization of the pre-existing ores, producing smaller discordant mineralized bodies.  相似文献   

14.
The discovery of the Gouap banded iron formations(BIFs)-hosted iron mineralization in the northwestern of the Nyong Group(Ntem Complex)in southwestern Cameroon provides unique insights into the geology of this region.In this contribution,we firstly report detailed study of geochemistry,isotopic and geochronology of well preserved samples of the Gouap BIFs collected from diamond drillcores.The Gouap BIFs consist mainly of amphibole BIFs and amphibole-pyrite BIFs characterized by dominant Fe2O3+SiO2contents and variable contents of CaO,MgO and SO3,consistent with the presence of amphibole,chlorite,epidote and pyrite,formed during amphibolite facies metamorphism and overprinted hydrothermal event.The amphibole–pyrite BIFs are typically enriched in trace and rare earth elements(REE)compared to the amphibole BIFs,suggesting the influence of detrital materials as well as secondary hydrothermal alteration.The Post Archean Australian Shale(PAAS)-normalized REE–Y profiles of the Gouap BIFs display positive La,Eu anomalies,weak negative Ce anomalies,indicating a mixture of low-temperature hydrothermal fluids and relatively oxic conditions probably under relative shallow seawater.We present here the first isotopic data of BIFs within the Ntem Complex.Theδ30SiNBS28values of the quartz from the Gouap BIFs vary from-1.5‰to-0.3‰and from-0.8‰to-0.9‰for the amphibole BIFs and amphibole–pyrite BIFs,respectively.The quartz hasδ18OV-SMOW values of 6.8‰–9.5‰(amphibole BIFs)and 9.2‰–10.6‰(amphibole–pyrite BIFs).The magnetite from the Gouap BIFs showsδ18O values ranging from-3.5‰to-1.8‰and from-3‰to-1.7‰for the amphibole BIFs and amphibole–pyrite BIFs,respectively.Moreover,the pyrite grains in the amphibole–pyrite BIFs displayδ34S values of 1.1‰–1.8‰.All isotopic data of the Gouap BIFs confirm that they might have precipitated from low-temperature hydrothermal fluids with detrital input distant from the volcanic activity.According to their geochemical and isotopic characteristics,we propose that the Gouap BIFs belong to the Superior type.In situ U–Pb zircon dating of BIFs was conducted to assess the BIF depositional age based on strong evidence of zircon in thin section.The Gouap BIFs were probably deposited at 2422±50 Ma in a region where sediments extended from continental shelf to deep-water environments along craton margins like the Caue Formation of the Minas Supergroup,Brazil.The studied BIFs have experienced regional hydrothermal activity and metamorphism at 2089±8.3 Ma during the Eburnean–Transamazonian orogeny.These findings suggest a physical continuity between the protocratonic masses of both Sao Francisco and Congo continents in the Rhyacian Period.  相似文献   

15.
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   

16.
The Pb–Zn ore deposits in the Guern Halfaya and Bou Grine areas (northern Tunisia) are hosted mainly by dolostones in the contact zone between Triassic and Upper Cretaceous strata and by Upper Cretaceous limestones. The deposits occur as lenticular, stratiform, vein, disseminations and stockwork ore bodies consisting of sphalerite, galena, pyrite, chalcopyrite and sulfosalt (gray copper). Barite and celestite dominate the gangue, with lesser calcite. The δ34S values of barite and celestite (12.7–15.0‰) at the Oum Edeboua mine are consistent with the reduction of sulfates in Triassic evaporites within the study area (12.8 < δ34S < 14.0‰). The δ34S values in base-metal sulfides from both study areas (2.6–9.5‰) and the presence of bacterial relics suggest involvement of bacterially-mediated sulfate reduction in the mineralization. The present Pb isotope data are homogeneous with 206Pb/204Pb, 207Pb/204Pb and 208Pb/204Pb ratios of 18.723–18.783, 15.667–15.685 and 38.806–38.889, respectively, which suggest a single source reservoir of Pb at depth in the upper crust. The syn-diagenetic mineralization in the Bahloul Formation and the calculated age from the Pb isotopic data suggest an Upper Cretaceous age for the Pb–Zn deposits in the Guern Halfaya and Bou Grine areas. During this period, NE–SW to ENE–WSW trending regional extensional tectonic structures likely favored migration of mineralizing fluids and eventual deposition at Guern Halfaya and Bou Grine.  相似文献   

17.
The Yukeng–Banling deposit is a typical fault-controlled hydrothermal Cu–Au deposit in the Shanmen Volcanic Basin (SVB), SE China. Ore bodies commonly occur as lodes, lenses and disconnected pods dipping SW with vertical zonation of ore minerals. Ore-related hydrothermal alteration is well developed on both sides of the veins, dominated by silicification, sericitization, chloritization and argillation with a banded alteration zonation. The mineralization can be divided into three stages (stages I, II and III). Native gold is present as veinlets in fractures of fine-grained pyrite from stage II.Zircon U–Pb and Rb–Sr isochron ages indicate that the Cu–Au mineralization is coeval with the Caomen alkaline granite and Xiaokeng quartz-diorite, both emplaced at ca. 102 Ma. Microthermometric measurements of fluid inclusions in quartz and sphalerite from stage II veins indicate that the Yukeng–Banling deposit is an epithermal deposit. Six ore-related quartz grains have δDH2O values of − 69 to − 43‰, and δ18OH2O values calculated using total homogenization temperatures that range from − 2.0 to 0.7‰. All samples plot in an area between the magmatic field and the meteoric line, suggesting that the ore-forming fluids are derived from a mixed source of magmatic and meteoric waters. δ34S values for eight pyrite separates range from − 2.1 to + 4.1‰ with an average of + 1.7‰, and δ34S values for galena and sphalerite are 2.3‰ and 2.2‰, similar to magmatic sulfur. Four alkaline granite samples have Pb isotopic ratios (206Pb/204Pb)t = 18.175–18.411, (207Pb/204Pb)t = 15.652–15.672 and (208Pb/204Pb)t = 38.343–38.800. Three quartz-diorite samples have ratios (206Pb/204Pb)t, (207Pb/204Pb)t and (208Pb/204Pb)t of 18.277–18.451, 15.654–15.693 and 38.673–38.846, respectively. These age-calculated lead isotopic data for alkaline granite are similar to those for the analyzed sulfides. Co/Ni ratios for stage II pyrites range from 1.42 to 5.10, indicating that the Yukeng–Banling deposit records the past involvement of magmatic hydrothermal fluids. The isotope data, together with geological, mineralogical and geochronological evidence, favor a primary magmatic source for sulfur and metals in the ore fluids. Mixing of the Cu- and Au-rich fluids with meteoric water led to precipitation of the Cu–Au veins along NW-trending faults.The Yukeng–Banling deposit, the contemporaneous Caomen alkaline granite and Xiaokeng quartz-diorite in the SVB formed under an extensional setting, due to high-angle subduction of the paleo-Pacific plate. The extensional setting facilitated the formation of Cu- and Au-rich magmas which was derived from enriched mantle and lower crust.  相似文献   

18.
The Chengchao iron deposit,the largest high-grade skarn iron deposit in southeastern Hubei Province,contains considerable amounts of magnetite and by-product anhydrite.To obtain better understanding of the ore-formation process,this study carried out He-Ar-S-Pb multi-isotopic analyses on the pyrites formed during two stages of mineralization.The results indicate that the δ~(34)S values(ranging from 14.0‰ to 17.6‰) of pyrites formed from the two stages have no obvious differences,suggesting that they were not derived from a single magmatic sulfur source.The δ~(34)S values of anhydrite mostly range from 21.9‰ to 28.4‰,similar to that of the Middle Triassic sedimentary anhydrite in the Middle-Lower Yangtze River metallogenic belt(MLYRB).The Pb isotopic compositions of the pyrites of both stages are homogeneous,with values of ~(208)Pb/~(204)Pb,~(207)Pb/~(204)Pb,and~(206)Pb/~(204)Pb being 38.006-38.257,15.523-15.556,and 17.806-18.052,respectively,indicating a mixed crust-mantle source.The He-Ar results exhibit different compositions of the two stages:the ~3He/~4He(R/Ra) and ~(40)Ar/~(36)Ar values for the early-stage pyrite are 0.46-0.63 and 311-322,respectively,whereas the values for late-stage pyrite are 0.23-0.34 and 305-361,respectively.Both stages of pyrites indicate the multiple sources of the ore-forming fluids,with decreasing amount of magmatic water and increasing amount of modified meteoric water(MASW) during fluid evolution.The Triassic evaporites played an important role in the mineralization process.  相似文献   

19.
安徽新桥块状硫化物矿床地球化学特征   总被引：6，自引：0，他引：6  
新桥块状硫化物矿床发育双层结构,地球化学特征也呈现出明显的“二元性”和垂向变化。下部网脉状蚀变矿化岩石SiO2、Al2O3、K2O和Na2O等含量较高,上部层状块状矿石和含矿岩石Fe2O3、FeO、CaO、MgO及SiO2等明显富集。稀土含量相对较低,上部层状块状矿层平均值为10.73×10-6,下部通道相蚀变矿化岩石平均值为126.1×10-6。重晶石δ34S值为+16.2‰,硬石膏δ34S值为+11.2‰,黄铁矿δ34S值为+1.5‰～+4.7‰。含矿硅质岩δ18O为+12.0‰～+13.9‰,下部通道相含黄铁矿石英脉δ18O值为+13.3‰～+18.6‰。自下部网脉状矿化到上部层状块状矿层,从粗晶细晶到变胶状胶状黄铁矿,δ34S、δ18O和δ30Si值逐渐降低,206Pb/204Pb、207Pb/204Pb和208Pb/204Pb平均值逐渐增高。  相似文献   

20.
The Tianqiao Pb–Zn deposit in the western Yangtze Block, southwest China, is part of the Sichuan–Yunnan–Guizhou (SYG) Pb–Zn metallogenic province. Ore bodies are hosted in Devonian and Carboniferous carbonate rocks, structurally controlled by a thrust fault and anticline, and carried about 0.38 million tons Pb and Zn metals grading > 15% Pb + Zn. Both massive and disseminated Pb–Zn ores occur either as veinlets or disseminations in dolomitic rocks. They are composed of ore minerals, pyrite, sphalerite and galena, and gangue minerals, calcite and dolomite. δ34S values of sulfide minerals range from + 8.4 to + 14.4‰ and display a decreasing trend from pyrite, sphalerite to galena (δ34Spyrite > δ34Ssphalerite > δ34Sgalena). We interpret that reduced sulfur derived from sedimentary sulfate (gypsum and barite) of the host Devonian to Carboniferous carbonate rocks by thermal–chemical sulfate reduction (TSR). δ13CPDB and δ18OSMOW values of hydrothermal calcite range from –5.3 to –3.4‰ and + 14.9 to + 19.6‰, respectively, and fall in the field between mantle and marine carbonate rocks. They display a negative correlation, suggesting that CO2 in the hydrothermal fluid was a mixture origin of mantle, marine carbonate rocks and sedimentary organic matter. Sulfide minerals have homogeneous and low radiogenic Pb isotope compositions (206Pb/204Pb = 18.378 to 18.601, 207Pb/204Pb = 15.519 to 15.811 and 208Pb/204Pb = 38.666 to 39.571) that are plotted in the upper crust Pb evolution curve and overlap with that of Devonian to Carboniferous carbonate rocks and Proterozoic basement rocks in the SYG province. Pb isotope compositions suggest derivation of Pb metal from mixed sources. Sulfide minerals have 87Sr/86Sr ratios ranging from 0.7125 to 0.7167, higher than Sinian to Permian sedimentary rocks and Permian Emeishan flood basalts, but lower than basement rocks. Again, Sr isotope compositions are supportive of a mixture origin of Sr. They have an Rb–Sr isotopic age of 191.9 ± 6.9Ma, possibly reflecting the timing of Pb–Zn mineralization. C–O–S–Pb–Sr isotope compositions of the Tianqiao Pb–Zn deposit indicate a mixed origin of ore-forming fluids, which have Pb–Sr isotope homogenized before the mineralization. The Permian flood basalts acted as an impermeable layer for the Pb–Zn mineralization hosted in the Devonian–Carboniferous carbonate rocks.  相似文献   

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