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1.
This study examines the rare-earth-elemenl and isotopic geochemistry of sulfide ores and associated rocks in the Bajiazi sulfide deposits of northeastern China. The distribution and concentration of rare earth elements (REE) in sulfide ores and associated rocks from the Bajiazi deposits have been determined by inductively coupled plasma spectroscopy (ICP) methods. Birdwing-shaped rare-earth-element profiles are only observed in granitic rocks at Bajiazi. Diverse rare-earth-element profiles of the ores and dolostones are different from those of granite and are interpreted to reflect an early sedimentary-diagenetic mineralization stage during which rare earth elements were added to the ores and host rocks. The characteristic features of the abundances of REE in the Bajiazi samples, including granite and sedimentary host rocks, are demonstrated by a variety of Eu anomalies in the chondrite-normalized REE pattern. Eu is the most mobile element, exhibiting increasingly negative anomalies in granite rock samples relative to the depletion of the sulfide ores and associated sedimentary host rocks, which are considered to be caused by preferential scavenging of Eu from sea water to sediments.

The δ34S values of sulfide minerals at Bajiazi generally range from ?12.3 to 14.2%, suggesting reduction both of marine sulfate and biogenic sources. The δ34S values from different ore types, sulfide minerals, and mines indicate a sedimentary exhalative origin, although they were, to some extent, homogenized during late overprinting. The late-stage sulfides from Bajiazi are isotopieally remarkably homogeneous and are significantly, although slightly, enriched in δ34S. These results imply multiple sources of sulfur derived from biogenic reduction, and/or sulfate in oceanic and/or connate waters, or from marine evaporites, and/or from magmatic hydrothermal sources. Isotopic temperatures from intersulfide fractionations (pyrite, sphalerite, and galena) range from 75° to 542°C, indicating the Bajiazi sulfide minerals have experienced different mineralizing stages.

Galena in the Bajiazi Proterozoic sediment-hosted Pb-Zn sulfide deposits has a very uniform Pb-isotope composition, with 206Pb/204Pb = 16.07 to 16.58, 207Pb/204Pb = 15.00 to 15.66, and 208Pb/204Pb = 36.13 to 36.92, suggesting that it all formed from a common mineralizing fluid. The variation of lead-isotopic values of ores is similar to that of their host sedimentary strata. The lead in the various ore types and host rocks within the Bajiazi district is virtually identical. Lead-isotope signatures, which generally plot very close to model crustal growth curves, characterized by a model age of ～1350 Ma, indicate a normal, nonradiogenic origin and an Early Proterozoic upper-crustal source for the lead in the ores. That lead was unrelated to the radiogenic lead in the Mesozoic granite.

The δ13C values range from +1 to ?5% PDB, and the δ18O values from ?6 to ?15% PDB. Later crystallization generations are enriched in the light isotopes of carbon and oxygen compared to early generations. The characteristics of carbon and oxygen isotopes of the Bajiazi deposits indicate that: (1) primary ores were precipitated in the Proterozoic marine environment; (2) both ores and host carbonates from the Bajiazi district are remarkably homogeneous in their carbon- and oxygen-isotope compositions during later tectonic, conlact-metamorphic stages; (3) although the variations in isotopic composition of carbon and oxygen are relatively small, a significant evolution toward a lighter isotopic composition with advancing diagenetic, tectonic, and contact metamorphic processes is observed; and (4) this evolution is independent of the presence or absence of ore minerals.  相似文献   

2.
Central Fujian Rift is another new and important volcanogenic massive sulfide Pb-Zn polymetallic metallogenetic belt. In order to find out the material genesis and mineralization period of Meixian-type Pb-Zn-Ag deposits, S and Pb isotope analysis and isotope geochronology of ores and wall rocks for five major deposits are discussed. It is concluded that the composition of sulfur isotope from sulfide ore vary slightly in different deposits and the mean value is close to zero with the 834S ranging from -3.5‰ to ＋5.6‰ averaging at ＋2.0‰, which indicates that the sulfur might originate from magma or possibly erupted directly from volcano or was leached from ore-hosted volcanic rock. The lead from ores in most deposits displays radioactive genesis character （206pb/204pb〉18.140, 207Pb/204pb〉15.584, 208pb/204pb〉38.569） and lead isotope values of ores are higher than those of wall rocks, which indicates that the lead was likely leached from the ore-hosted volcanic rocks. Based on isotope data, two significant Pb-Zn metallogenesis are delineated, which are Mid- and Late-Proterozoic sedimentary exhalative metailogenesis （The single zircon U-Pb, Sm-Nd isochronal and Ar-Ar dating ages of ore- hosted wall rocks are calculated to be among 933-1788 Ma.） and Yanshanian magmatic hydrothermal superimposed and alternated metallogenesis （intrusive SHRIMP zircon U-Pb and Rb-Sr isochronal ages between 127-154 Ma）.  相似文献   

3.
Summary The Dachang Sn-polymetallic ore district is one of the largest tin producing districts in China. Its origin has long been in dispute between magmatic-hydrothermal replacement and submarine exhalative-hydrothermal origin. The Dachang ore district comprises several types of ore deposits, including the Lamo magmatogenic skarn deposit near a granite intrusion, the Changpo-Tongkeng bedded and vein-type sulfide deposit, and the Gaofeng massive sulfide deposit. Sulfide minerals from the Lamo skarn ores show δ34S values in the range between −3 and +4‰ with a mean close to zero, suggesting a major magmatic sulfur source that likely was the intrusive Longxianggai granite. Sulfide minerals from the Gaofeng massive ores show higher δ34S values between +5 and +12‰, whereas sulfide minerals from the Changpo-Tongkeng bedded ores display lighter δ34S values between −7 and −0.2‰. The difference in the sulfur isotope ranges in the two deposits can be interpreted by different degrees of inorganic thermochemcial reduction of marine sulfate using a one-step batch separation fractionation model. Sulfur isotopic compositions from the vein-type ores at Changpo-Tongkeng vary widely from −8 to +4‰, but most of the data cluster around −2.9‰, which is close to that of bedded ores (−3.6‰). The sulfur in vein-type ores might be derived from bedded ores or it represents a mixture of magmatic- and sedimentary-derived sulfur. Pb isotopic compositions of sulfide minerals in the Dachang ore district reveal a difference between massive and bedded ores, with the massive ores displaying more radiogenic Pb isotope ratios. Correlations of 206Pb/204Pb and 207Pb/204Pb or 208Pb/204Pb for the massive and bedded ores are interpreted as two-component mixing of Pb leached from sedimentary host rocks and from deep-seated Precambrian basement rocks composed of metamorphosed volcano-sedimentary rocks. Pb isotopic compositions of sulfide minerals from vein-type ores overlap with those of bedded sulfides. Similar to the sulfur, the lead in vein-type ores might be derived from bedded ores. Skarn ores at Lamo show very limited variations in Pb isotopic compositions, which may reflect a major magmatic-hydrothermal lead source. Helium isotope data of fluid inclusions trapped in sulfides indicate that He in the massive and bedded ores has a different origin than He in fluorite of granite-related veins. The 3He/4He ratios of 1.2–2.9 Ra of fluid inclusions from sulfides at Gaofeng and Changpo-Tongkeng imply a contribution of mantle-derived fluids. Overall our data support a submarine exhalative-hydrothermal origin for the massive and bedded ore types at Dachang. Supplementary material to this paper is available in electronic form at Appendix available as electronic supplementary material  相似文献   

4.
Lead isotope analyses of 25 sulfide samples (galenas, iron sulfides, and sulfosalts) from five different mines of the Skellefte district, northern Sweden, demonstrate that the Pb-isotopic composition of galenas and other sulfides rich in lead varies between individual deposits within the district. This contrasts with many other base-metal districts, where ore lead is isotopically homogeneous on a regional basis. Although all of the Skellefte leads are depleted in 207Pb relative to average global lead evolution models, thus suggesting a large mantle-derived component in their sources, the Nasliden deposit lying at the contact of the host volcanic rocks and the overlying metasediments contains a significant component of crustal lead. It is concluded that while the Pb-isotope data are consistent with a volcanic exhalative origin of the ores of the Skellefte district, they also demonstrate that older crustal lead was incorporated into the sulfides during their emplacement and the subsequent period of magmatic and metamorphic activity which followed their deposition.  相似文献   

5.
The Huangshaping Pb–Zn–W–Mo polymetallic deposit, located in southern Hunan Province, China, is one of the largest deposits in the region and is unique for its metals combination of Pb–Zn–W–Mo and the occurrence of significant reserves of all these metals. The deposit contains disseminated scheelite and molybdenite within a skarn zone located between Jurassic granitoids and Carboniferous sedimentary carbonate, and sulfide ores located within distal carbonate-hosted stratiform orebodies. The metals and fluids that formed the W–Mo mineralization were derived from granitoids, as indicated by their close spatial and temporal relationships. However, the source of the Pb–Zn mineralization in this deposit remains controversial.Here, we present new sulfur, lead, and strontium isotope data of sulfide minerals (pyrrhotite, sphalerite, galena, and pyrite) from the Pb–Zn mineralization within the deposit, and these data are compared with those of granitoids and sedimentary carbonate in the Huangshaping deposit, thereby providing insights into the genesis of the Pb–Zn mineralization. These data indicate that the sulfide ores from deep levels in the Huangshaping deposit have lower and more consistent δ34S values (− 96 m level: + 4.4‰ to + 6.6‰, n = 13) than sulfides within the shallow part of the deposit (20 m level: + 8.3‰ to + 16.3‰, n = 19). The δ34S values of deep sulfides are compositionally similar to those of magmatic sulfur within southern Hunan Province, whereas the shallower sulfides most likely contain reduced sulfur derived from evaporite sediments. The sulfide ores in the Huangshaping deposit have initial 87Sr/86Sr ratios (0.707662–0.709846) that lie between the values of granitoids (0.709654–0.718271) and sedimentary carbonate (0.707484–0.708034) in the Huangshaping deposit, but the ratios decreased with time, indicating that the ore-forming fluids were a combination of magmatic and formation-derived fluids, with the influence of the latter increasing over time. The lead isotopic compositions of sulfide ores do not correlate with sulfide type and define a linear trend in a 207Pb/204Pb vs. 206Pb/204Pb diagram that is distinct from the composition of the disseminated pyrite within sedimentary carbonates and granitoids in the Huangshaping deposit, but is similar to the lead isotopic composition of sulfides within coeval skarn Pb–Zn deposits in southern Hunan Province. In addition, the sulfide ores have old signatures with relative high 207Pb/206Pb ratios, suggesting that the underlying Paleoproterozoic basement within southern Hunan Province may be the source of metals within the Huangshaping deposit.The isotope geochemistry of sulfide ores in the Huangshaping deposit shows a remarkable mixed source of sulfur and ore-forming fluids, and the metals were derived from the basement. These features are not found in representative skarn-type Pb–Zn mineralization located elsewhere. The ore-forming elements (S, Pb, and Zn) from the granitoids made an insignificant contribution to sulfide precipitation in this deposit. However, the emplacement of granitoids did provide large amounts of heat and fluids to the hydrothermal system in this area and extracted metals from the basement rocks, indicating that the Jurassic magmatism associated with the Huangshaping deposit was crucial to the Pb–Zn mineralization.  相似文献   

6.
We have studied Pb isotopic systems of K-feldspar, pyrite, and pyrrhotine from gabbroids and ore of the Velimyaki Early Proterozoic massif in the northern Ladoga region in the southeastern part of the Fennoscandian Shield. The isochronous Pb–Pb age of sulfides has been determined as ～450 Ma, which corresponds to intersection of the regression line with the lead accumulation curve with μ = 10.4–10.8; the model Pb age of sulfides is close to isochronous under the condition that the composition of lead evolved from a geochemical reservoir with an age of 1.9 Ga. The isotopic parameters of the lead in sulfides and K-feldspar indicate their formation in upper crust conditions (μ = 238U/204Pb > 10). From the obtained data, it follows that the isotopic composition of lead in K-feldspar corresponds to a Proterozoic age (1890 Ma) of magmatic crystallization of the rocks in the massif, and strongly radiogenic lead sulfides testify, with the greatest probability, to the later (Caledonian) formation of sulfide ores.  相似文献   

7.
红山铜-多金属矿床位于滇西中甸红山一带,主矿体是一个石榴子石型夕卡岩矿床。野外考察中发现了一个叠加在夕卡岩矿体之上的热泉喷流构造,它保存了具典型热泉喷流特征的喷口。喷口附近产出近水平层状的含铁硅质岩中硫化物的硫同位素δ34S为3.73‰~5.57‰,平均值5.08‰;铅同位素206Pb/204Pb和207Pb/204Pb比值分别为18.670~18.808和15.614~15.784,其硫、铅同位素组成与滇西地区喜马拉雅期斑岩和斑岩矿床的硫、铅同位素组成相似,暗示红山矿区有新生代的岩浆活动和成矿作用。该区新生代热泉喷流成矿作用的发现既丰富了对滇西中甸地区成矿作用的认识,也对红山铜-多金属矿床的成因有了更全面的了解,为该区进一步扩展找矿远景提供了重要依据。  相似文献   

8.
The Barite Hill gold deposit, at the southwestern end of the Carolina slate belt in the southeastern United States, is one of four gold deposits in the region that have a combined yield of 110 metric tons of gold over the past 10 years. At Barite Hill, production has dominantly come from oxidized ores. Sulfur isotope data from hypogene portions of the Barite Hill gold deposit vary systematically with pyrite–barite associations and provide insights into both the pre-metamorphic Late Proterozoic hydrothermal and the Paleozoic regional metamorphic histories of the deposit. The δ34S values of massive barite cluster tightly between 25.0 and 28.0‰, which closely match the published values for Late Proterozoic seawater and thus support a seafloor hydrothermal origin. The δ34S values of massive sulfide range from 1.0 to 5.3‰ and fall within the range of values observed for modern and ancient seafloor hydrothermal sulfide deposits. In contrast, δ34S values for finer-grained, intergrown pyrite (5.1–6.8‰) and barite (21.0–23.9‰) are higher and lower than their massive counterparts, respectively. Calculated sulfur isotope temperatures for the latter barite–pyrite pairs (Δ=15.9–17.1‰) range from 332–355 °C and probably reflect post-depositional equilibration at greenschist-facies regional metamorphic conditions. Thus, pyrite and barite occurring separately from one another provide pre-metamorphic information about the hydrothermal origin of the deposit, whereas pyrite and barite occurring together equilibrated to record the metamorphic conditions. Preliminary fluid inclusion data from sphalerite are consistent with a modified seawater source for the mineralizing fluids, but data from quartz and barite may reflect later metamorphic and (or) more recent meteoric water input. Lead isotope values from pyrites range for 206Pb/204Pb from 18.005–18.294, for 207Pb/204Pb from 15.567–15.645, and for 208Pb/204Pb from 37.555–38.015. The data indicate derivation of the ore leads from the country rocks, which themselves show evidence for contributions from relatively unradiogenic, mantle-like lead, and more evolved or crustal lead. Geological relationships, and stable and radiogenic isotopic data, suggest that the Barite Hill gold deposit formed on the Late Proterozoic seafloor through exhalative hydrothermal processes similar to those that were responsible for the massive sulfide deposits of the Kuroko district, Japan. On the basis of similarities with other gold-rich massive sulfide deposits and modern seafloor hydrothermal systems, the gold at Barite Hill was probably introduced as an integral part of the formation of the massive sulfide deposit. Received: 17 August 1998 / Accepted: 12 October 2000  相似文献   

9.
The Bainiuchang deposit in Yunnan Province,China,is located geographically between the Gejiu ore field and the Dulong ore field.In addition to the>7000 t Ag reserves,the deposit also boasts of large-scale Pb,Zn and Sn reserves with a lot of dispersed elements(In,Cd,Ge,Ga,etc.).We have determined systematically the Pb isotope composition of the deposit.The Pb isotope ratios of the ores that are of sea-floor exhalative sedimentary origin in the northwest of the mining district,are ~(206)Pb/~(204)Pb=17.758-18.537,~(207)pb/~(204)pb=15.175-15.862 and ~(208)pb/~(204)pb=37.289-39.424,while those of ores that are of magmatic hydrothermal superimposition origin in the southeast of the mining district, are ~(206)Pb/~(204)Pb=17.264-18.359,~(207)Pb/~(204)Pb=14.843-15.683 and ~(208)Pb/~(204)Pb=36.481-38.838, respectively.In terms of the Pb isotope composition of feldspar in magmatic rocks or magmatic whole- rock samples from the mining district,we have determined the Pb isotope composition and acquired the Pb isotope ratios as:~(206)Pb/~(204)Pb=18.224-18.700,~(207)Tpb/~(204)Pb=15.595-15.797 and ~(208)Pb/~(204)Pb= 38.193-39.608.Then,in the light of the Pb isotope composition of metamorphic rock samples from the Proterozoic basement exposed in the Dulong ore field,we have determined the Pb isotope composition and obtained the isotope ratios as:~(206)Pb/~(204)Pb=18.434-19.119,~(207)Pb/~(204)Pb=15.644-15.693,and ~(208)Pb/~(204)Pb=38.514-38.832.And the Pb isotope ratios of Cambrian sedimentary rocks,which are exposed in the Bainiuchang mining district,are ~(206)Pb/~(204)Pb=18.307-19.206,~(207)Pb/~(204)Pb= 15.622-15.809,and ~(206)Pb/~(204)Pb=38.436-39.932.By comparing the two types of ores with respect to their Pb isotope compositions,it is indicated that lead in the Bainiuchang deposit was derived largely from the lower-crust granulite which is earlier than Neoproterozoic in age,but the Yanshanian magmatic hydrothermal fluids probably provided a part of ore-forming elements such as Sn for the ore blocks in the south of the mining district.  相似文献   

10.
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   

11.
The Huogeqi orefield located on the northern side of Mt. Langshan, Inner Mongolia occurs in the Middle Proterozoic Langshan Group metamorphic rocks, and the orebodies arc stratiform. In the past twenty years, many Chinese geologists have conducted researches on the Huogeqi Cu-Pb-Zn deposit, but there has been still a controversy on its origin. Some advocate that the deposit is of sedimentary-metamorphic rcworking origin, some hold that it is of sea-floor SEDEX origin, and others have a preference for magmatic superimposition origin. The crux of the controversy is that there is no common understanding about the source of ore-forming materials. In this paper, the Pb isotopic compositions of regional Achaean-Early Proterozoic basement rocks, various types of sedimentary- metamorphic rocks and volcanic rocks in the mining district, Late Proterozoic and Hercynian magmatic rocks arc introduced and compared with the orc-lead composition, so as to constrain the source of the ore lead. The result indicates that （1） sulfides in the ores have homogeneous Pb isotopic compositions, showing a narrow variation range. Their ^206pb/^204pb ratios arc within a range of 17.027- 17.317; ^207Pb/^204pb ratios, 15.451-15.786 and ^208Pb/^204pb ratios, 36.747-37.669; （2） the Pb isotopic compositions of the regional Achaean-Early Proterozoic basement rocks arc characteristic of the old Pb isotopic composition at the early-stage evolution of the Earth, which varies over a wider range, reflecting significant differences in Pb isotopic compositions of the ores. All this indicates that the source of ore lead has no bearing on the basement rocks; （3） the sedimentary-metamorphic rocks in the mining district arc characterized by highly variable and more radiogenic Pb isotopic compositions and their Pb isotopic ratios arc obviously higher than those of ores, demonstrating that ore lead did not result from metamorphic rcworking of these rocks; （4） Pb isotopic compositions of Late Proterozoic diorite-gabbro and Hercynian granite are higher than those of ores. Meanwhile, the Pb isotopic compositions of sulfides in the small-sized strata-penetrating mineralized veinlets formed at later stages arc completely consistent with that of sulfides in stratiform-banded ores, suggesting that these veiniets arc the product of autochthonous rcworking of the stratiform-banded ores during the period of metamorphism and the late magmatic superimposition-mineralization can be excluded; （5） amphibolite, whose protolith is basic volcanic rocks, has the same Pb isotopic compositions as ores, implying that ore lead was derived probably from basic volcanism. So, the source of ore-forming materials for the Huogeqi deposit is like that of the volcanic massive sulfide （VMS） deposits. However, the orebodies do not occur directly within the volcanic rocks, and instead they overlie the volcanic rocks, showing some differences from those typical VMS-type deposits.  相似文献   

12.
为了探讨西藏墨竹工卡县洞中拉铅锌矿的成矿物质来源,研究矿床成矿机制,对该矿床的矿石样品进行了硫和铅同位素分析,并对其变化规律和成因意义进行讨论。研究结果表明,6件金属硫化物样品(闪锌矿、黄铜矿、方铅矿)的δ34S值变化于2.2‰～4.8‰之间,显示硫同位素组成比较稳定。根据共生硫化物对所确定的温度,该矿床属中低温热液矿床。6件金属硫化物样品206Pb/204Pb、207Pb/204Pb和208Pb/204Pb变化范围分别为18.628 0～18.629 6、15.698 0～15.699 9、39.077 5～39.082 4,平均值分别为18.628 70、15.699 02和39.079 37。硫和铅同位素研究结果表明,洞中拉铅锌矿床的硫主要来自沉积围岩,主要为无机还原成因,有少量硫来自本地区燕山晚期花岗岩;洞中拉铅锌矿床矿石铅主要来自上地壳物质。  相似文献   

13.
The Tiemurt Pb-Zn-Cu deposit (metal reserve: 0.29 Mt (Pb + Zn) and 0.14 Mt Cu) is hosted in the Kangbutiebao Formation volcanic-sedimentary rocks in the Chinese Altay Orogen, NW China. Although some geological and geochemical characteristics of primary seafloor sedimentary mineralization are preserved, major fault-controlled Pb-Zn-Cu orebodies are adjacent to the Sarekbuobu orogenic gold deposit, and therefore it is also interpreted to be closely related to regional deformational-metamorphic processes. The seafloor sedimentary mineralization is evidenced by the occurrence of the banded ores and marine sulfate-originated sulfur isotopic compositions of the sulfides (bimodal δ34S values of 17.29–18.67‰ and −25.03 to −17.58‰). The lead isotope compositions accord with the evolution line of mantle, implying that the Pb were chiefly sourced from the mantle-reservoir. The later deformational and metamorphic overprinting are recorded by the fault-controlled lodes with ore textures of epigenetic infilling and replacement. Besides well-developed CO2-rich fluid inclusions, the D-O isotopic data of the overprinting fluids fall into the area between metamorphic fluids and meteoric water line, indicative of metamorphic fluids origin with meteoric water involvement. To further trace the Pb-Zn-Cu accumulation and remobilization processes, systematic in-situ trace elements in sulfides of different generations are analyzed using LA-ICP-MS. Ti-Mn-Cu-Pb-Zn-Bi concentrations in pyrite show a trend of progressive decrease from early to late generations. Similar decreasing trends of trace element concentrations are also present in sphalerite, galena, chalcopyrite and pyrrhotite, although the combinations of trace element are slightly different. This indicates that the ore-forming metals (esp. Cu, Pb and Zn) were initially locked up in the crystal lattice of the VMS sulfides (especially pyrite). Deformational and metamorphic processes of the primary ores during the Permian-Triassic collisional orogeny have likely led to trace element remobilization and sulfides purification, which redistributed the metals and upgraded the ores. Combined with previous studies, we proposed that the Pb-Zn-Cu of Tiemurt had been accumulated from seafloor sedimentation (ca. 400 Ma) to deformation-metamorphism processes (ca. 240 Ma).  相似文献   

14.
Early Proterozoic volcanic and sedimentary rocks of the Rappen district in northern Sweden were deposited at a destructive plate margin to the south of the Archaean craton of the western Baltic Shield. The volcano-sedimentary suite was intruded by two generations of early Proterozoic granites at ca. 1.89–1.85 Ga and ca.1.82–1.78 Ga, respectively, and metamorphosed at upper amphibolite facies conditions. Small stratabound iron, copper, and zinc deposits occur in felsic to mafic tuffs and arkosic sediments. Small deposits of molybdenum, tungsten, and uranium formed during the emplacement of the younger granites. The lead isotopic compositions of sulfide trace lead from the various deposits are highly heterogeneous. In the 206Pb/204Pb–207Pb/204Pb diagram they fall on mixing arrays between little evolved early Proterozoic lead and highly radiogenic Caledonian lead. The least radiogenic lead isotopic compositions from the various deposits have a wide range of 207Pb/204Pb ratios and thus indicate variable involvement of Archaean crustal lead in the Proterozoic deposits. Deposits hosted by siliciclastic rocks have higher 207Pb/204Pb ratios than deposits hosted in mafic to felsic tuffites. The lead isotopic heterogeneity suggests that the lead in the various deposits was locally derived and, furthermore, that the sedimentary rocks in part originated from the Archaean craton to the north. Lead mixing arrays in the 206Pb/204Pb–207Pb/204Pb diagram demonstrate that in Paleozoic time radiogenic lead was mobilized and transported in the basement. Source ages calculated from the mixing arrays (ca.1.9 Ga and ca.1.8 Ga) correspond to the age of the Early Proterozoic volcanism and metamorphism respectively. One group of deposits includes lead from at least three sources and illustrates that radiogenic lead was multiply mobilized and transported in the Proterozoic basement. It occurs in deposits that occur in zones that became permeable during the reactivations of the basement.  相似文献   

15.
The Bianbianshan deposit, the unique gold-polymetal (Au-Ag-Cu-Pb-Zn) veined deposit of the polymetal metallogenic belt of the southern segment of Da Hinggan Mountains mineral province, is located at the southern part of the Hercynian fold belt of the south segment of Da Hinggan Mountains mineral province, NE China. Ores at the Bianbianshan deposit occur within Cretaceous andesite and rhyolite in the form of gold-bearing quartz veins and veinlet groups containing native gold, electrum, pyrite, chalcopyrite, galena and sphalerite. The deposit is hosted by structurally controlled faults associated with intense hydrothermal alteration. The typical alteration assemblage is sericite + chlorite + calcite + quartz, with an inner pyrite - sericite - quartz zone and an outer seicite - chlorite - calcite - epidote zone between orebodies and wall rocks. δ34 S values of 17 sulfides from ores changing from –1.67 to +0.49‰ with average of –0.49‰, are similar to δ34 S values of magmatic or igneous sulfide sulfur. 206Pb/204Pb, 207Pb/204Pb and 208Pb/ 204Pb data of sulfide from ores range within 17.66–17.75, 15.50–15.60, and 37.64–38.00, respectively. These sulfur and lead isotope compositions imply that ore-forming materials might mainly originate from deep sources. H and O isotope study of quartz from ore-bearing veins indicate a mixed source of deep-seated magmatic water and shallower meteoric water. The ore formations resulted from a combination of hydrothermal fluid mixing and a structural setting favoring gold-polymetal deposition. Fluid mixing was possibly the key factor resulting in Au-Ag-Cu-Pb-Zn deposition in the deposit. The metallogenesis of the Bianbianshan deposit may have a relationship with the Cretaceous volcanic-subvolcanic magmatic activity, and formed during the late stage of the crust thinning of North China.  相似文献   

16.
Lead isotope compositions of nine sulfide concentrates from ore samples from the Sar-Cheshmeh deposit are reported. They range from virtually unaltered granodiorite through varying degrees of potassic alteration to ores showing strong phyllic alteration (sericite veins). The samples without strong phyllic alteration have fairly uniform lead isotope compositions around 206Pb/204Pb=18.6, 207Pb/204Pb=15.6, and 208Pb/204Pb=38.7. Two samples with sericite veins have markedly more radiogenic lead. It is concluded that the fluid responsible for the potassic alteration and the associated mineralization was essentially magmatic, whereas convecting meteoric water from the country rock acted as a mineralizing solution during phyllic alteration. In the context of the plumbotectonics model, the deposit has a typical orogen signature intermediate between primitive and mature island-arc settings.  相似文献   

17.
Mesothermal vein-type Sb mineralization in the Rheinisches Schiefergebirge, Germany, is characterized by two different mineralization styles, which are (1) extensional quartz-stibnite vein systems, and (2) (Cu)-Pb-Sb sulphosalt assemblages in overprinted pre-existing Pb-Zn veins. A detailed Pb isotope study of 52 representative samples from both mineralization types indicates distinct compositional patterns. (Cu)-Pb-Sb sulphosalts (meneghinite, boulangerite, bournonite) formed by reaction/remobilization are characterized by Pb isotope compositions (206Pb/204Pb=18.179-18.223), which are identical to the precursor galena (206Pb/204Pb=18.168-18.223). The Pb isotope composition of sulphosalt minerals in these vein systems was controlled by lead inherited from pre-existing galena. Stibnite and Pb-sulphosalts (zinkenite, semseyite, plagionite) formed in quartz-stibnite vein systems display Pb isotope ratios (206Pb/204Pb=18.250-18.354), which are more radiogenic than galenas from Variscan Pb-Zn ore veins (206Pb/204Pb=18.162-18.303). Detailed small-scale investigation of thrust zones hosting Pb-Zn ores and crosscutting quartz-ankerite fissure veins (Ramsbeck deposit) indicates that the Pb isotope compositions of recrystallized (galena) and remobilized phases (boulangerite, semseyite, bournonite) are arranged along a linear trend. This is interpreted as mixing between primary galena with 206Pb/204Pb᜞.206 and overprinting hydrothermal fluids with a more radiogenic composition (206Pb/204Pb⁾.354), expressed by intermediate compositions (206Pb/204Pb=18.256-18.334) of newly-formed sulphosalts. The Pb isotope systematics of the vein-type Sb mineralization is in accordance with a model of Pb extraction from similar crustal sources (Palaeozoic sedimentary sequences) at different times.  相似文献   

18.
The Hammam Zriba F-Ba-(Zn-Pb) ore deposit in the Province of Zaghouan in north-eastern Tunisia is hosted in the shallow dipping unconformity between green marls with chalky biomicritic limestones of Campanian age and Uppermost Jurassic carbonates. The mineralization consists mainly of fluorite and barite with minor sphalerite and galena. Calcite is the main gangue mineral. Two types of Zn-Pb sulfides can be distinguished according to the geometry of the orebodies, i.e., lenticular or stratiform ores, intra-karstic fillings. Sulfur isotope compositions (δ34S) of barite range from 14.7 to 17.2‰, indicating that sulfur was derived from Triassic evaporites and the higher ones (19–25.7‰) are due to reservoir effect associated with thermo-chemical sulfate reduction (TSR) or bacterial sulfate reduction (BSR) under conditions of restricted sulfate supply. δ34S of galena and sphalerite in lenticluar and intra-karstic orebodies range from −13.8 to 2.1‰, and could be explained by multiple sources of reduced sulfur: Triassic evaporites, diagenetic primary sulfides as well as sulfur from organic matter. Both TSR and BSR as potential contributors of sulfur are needed for sulfide precipitation. Lead isotope compositions of galena exhibit very similar: 206Pb/204Pb (18.858–18.876), 207Pb/204Pb (15.667–15.684), and 208Pb/204Pb (38.680–38.747) ratios, and plot between the upper crust and orogene average growth curves, reflecting involvement of a mixing and subsequent homogenization of Pb isotopic compositions of different source Pb reservoirs. The underlying Paleozoic basement rocks were the plausible source of metals. The economic ore (fluorite F1) mineralization was formed during the Eocene-Miocene compressional phase. During this deformation phase, deep-seated basinal brines have been circulated as hydrothermal fluids that have interacted with the Paleozoic rocks, thereby leaching metals, and have been channelized through subsidiary faults associated with the major regional NE–SW-trending deep-seated Zaghouan-Ressas fault. Hydrothermal fluids then migrated to the site of deposition where they got mixed with shallow, cooler, metal-depleted, TSR- and BSR-derived sulfur-rich fluids, which triggered the precipitation of the ores.  相似文献   

19.
The Shanshulin Pb–Zn deposit occurs in Upper Carboniferous Huanglong Formation dolomitic limestone and dolostone, and is located in the western Yangtze Block, about 270 km west of Guiyang city in southwest China. Ore bodies occur along high angle thrust faults affiliated to the Weishui regional fault zone and within the northwestern part of the Guanyinshan anticline. Sulfide ores are composed of sphalerite, pyrite, and galena that are accompanied by calcite and subordinate dolomite. Twenty-two ore bodies have been found in the Shanshulin deposit area, with a combined 2.7 million tonnes of sulfide ores grading 0.54 to 8.94 wt.% Pb and 1.09 to 26.64 wt.% Zn. Calcite samples have δ13CPDB and δ18OSMOW values ranging from − 3.1 to + 2.5‰ and + 18.8 to + 26.5‰, respectively. These values are higher than mantle and sedimentary organic matter, but are similar to marine carbonate rocks in a δ13CPDB vs. δ18OSMOW diagram, suggesting that carbon in the hydrothermal fluid was most likely derived from the carbonate country rocks. The δ34SCDT values of sphalerite and galena samples range from + 18.9 to + 20.3‰ and + 15.6 to + 17.1‰, respectively. These values suggest that evaporites are the most probable source of sulfur. The δ34SCDT values of symbiotic sphalerite–galena mineral pairs indicate that deposition of sulfides took place under chemical equilibrium conditions. Calculated temperatures of S isotope thermodynamic equilibrium fractionation based on sphalerite–galena mineral pairs range from 135 to 292 °C, consistent with previous fluid inclusion studies. Temperatures above 100 °C preclude derivation of sulfur through bacterial sulfate reduction (BSR) and suggest that reduced sulfur in the hydrothermal fluid was most likely supplied through thermo-chemical sulfate reduction (TSR). Twelve sphalerite samples have δ66Zn values ranging from 0.00 to + 0.55‰ (mean + 0.25‰) relative to the JMC 3-0749L zinc isotope standard. Stages I to III sphalerite samples have δ66Zn values ranging from 0.00 to + 0.07‰, + 0.12 to + 0.23‰, and + 0.29 to + 0.55‰, respectively, showing the relatively heavier Zn isotopic compositions in later versus earlier sphalerite. The variations of Zn isotope values are likely due to kinetic Raleigh fractional crystallization. The 206Pb/204Pb, 207Pb/204Pb and 208Pb/204Pb ratios of the sulfide samples fall in the range of 18.362 to 18.573, 15.505 to 15.769 and 38.302 to 39.223, respectively. The Pb isotopic ratios of the studied deposit plot in the field that covers the upper crust, orogenic belt and mantle Pb evolution curves and overlaps with the age-corrected Proterozoic folded basement rocks, Devonian to Lower Permian sedimentary rocks and Middle Permian Emeishan flood basalts in a 207Pb/204Pb vs. 206Pb/204Pb diagram. This observation points to the derivation of Pb metal from mixed sources. Sphalerite samples have 87Sr/86Sr200 Ma ratios ranging from 0.7107 to 0.7115 similar to the age-corrected Devonian to Lower Permian sedimentary rocks (0.7073 to 0.7111), higher than the age-corrected Middle Permian basalts (0.7039 to 0.7078), and lower than the age-corrected Proterozoic folded basement (0.7243 to 0.7288). Therefore, the Sr isotope data support a mixed source. Studies on the geology and isotope geochemistry suggest that the Shanshulin deposit is a carbonate-hosted, thrust fault-controlled, strata-bound, epigenetic, high grade deposit formed by fluids and metals of mixed origin.  相似文献   

20.
H. Sun  J. Wu  P. Yu  J. Li 《Mineralium Deposita》1998,34(1):102-112
The Jingtieshan deposit occurs in a Precambrian tectonic-stratigraphic terrane within the Northern Qilian Caledonian Orogen, and is generally considered as a Superior-type iron formation. The deposit is characterized by Fe-Si-Ba and Cu mineralization and consists of two types of orebodies, an upper jasper-barite-iron deposit and a lower copper sulfide deposit. The iron orebodies occur as independent stratigraphic layers concordant within a thick argillaceous succession, and exhibit fine-grained textures and well-developed sedimentary layering. The ores are predominantly composed of specularite and jasper with lesser amounts of magnetite, hematite, siderite, and barite. The presence of barite, hematite and jasper as major components shows that the iron ores were precipitated in a relatively oxidized ocean floor environment. The Cu orebody directly underlies the iron ore and is hosted by chlorite-sericite-quartz phyllite. The Cu mineralization is composed of pyrite and chalcopyrite and is characterized by stockwork. The disseminated and stockwork Cu mineralization is metamorphosed and concordant with respect to foliation, indicating pre-fabric development, i.e. pre-metamorphism, and was probably originally formed by reduced fluids reacting at the base of and within the oxide iron formation. Geochemical data show that the jasper-barite-iron ores, which resemble Superior-type iron formations, have a high input of hydrothermal-hydrogeneous elements (SiO2, av.=56%; Fe2O3t, av.=30%; Mn, av.=0.45%; BaO, av.=16.7%) with minimal terrigeneous input (<15% combined Al2O3, TiO2, K2O, MgO, etc.). The δ34S of exhalative barite varies from 28 to 34‰, which is very heavy with respect to other Late Proterozoic sulfate-bearing deposits, except those of circa 600 Ma in which the sulfides range from 8 to 20‰. The sulfur isotope data indicate that the barite was formed by the mixing of a Ba-rich hydrothermal fluid with sulfate-rich ambient seawater and that the sulfides ores were most probably derived from the reduction of seawater sulfate during subsurface reaction with ferrous iron-bearing minerals. These data are consistent with the jasper-barite-iron deposit forming by hydrothermal exhalative and chemical sedimentary processes on the floor of an ocean basin, and with the Cu mineralization forming by hydrothermal filling and replacement in base of and within the iron formation. Received: 19 March 1997 / Accepted: 14 May 1998  相似文献   

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