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1.
The Valentine wollastonite skarn in the north-west Adirondack Mountains, New York, is a seven million ton deposit which resulted from channellized infiltration of H2O-rich, silica-bearing fluids. The wollastonite formed by reaction of these fluids with non-siliceous calcite marble. The skarn formed at the contact of the syenitic Diana Complex and was subsequently overprinted by Grenville-age granulite facies metamorphism and retrograde hydrothermal alteration during uplift. Calcite marbles adjacent to the deposit have generally high δ18O values (c. 21‰), typical of Grenville marbles which have not exchanged extensively with externally derived fluids. Carbon isotopic fractiona-tions between coexisting calcite and graphite in the marbles indicate equilibration at 675d? C, consistent with the conditions of regional metamorphism. Oxygen isotopic ratios from wollastonite skarn are lower than in the marbles and show a 14‰ variation (-1‰ to 13‰). Some isotopic heterogeneity is preserved from skarn formation, and some represents localized exchange with low-δ18O retrograde fluids. Detailed millimetre- to centimetre-scale isotopic profiles taken across skarn/marble contacts reveal steep δ18O gradients in the skarn, with values increasing towards the marble. The gradients reflect isotopic evolution of the fluid as it reacted with high δ18O calcite to form wollastonite. Calcite in the marble preserves high δ18O values to within <5 mm of the skarn contact. The preservation of high δ18O values in marbles at skarn contacts and the disequilibrium fractionation between wollastonite skarn and calcite marble across these contacts indicate that the marbles were not infiltrated with significant quantities of the fluid. Thus, the marbles were relatively impermeable during both the skarn formation and retrograde alteration. Skarn formation may have been episodic and fluid flow was either chaotic or dominantly parallel to lithological contacts. Although these steep isotope gradients resemble fluid infiltration fronts, they actually represent the sides of the major flow system. Because chromatographic infiltration models of mass transport require the assumption of pervasive fluid flow through a permeable rock, such models are not applicable to this hydrothermal system and, by extension, to many other metamorphic systems where low-permeability rocks restrict fluid migration pathways. Minimum time-integrated fluid fluxes have been calculated at the Valentine deposit using oxygen isotopic mass balance, reaction progress of fluid buffering reactions, and silica mass balance. All three approaches show that large volumes of fluid were necessary to produce the skarn, but silica mass balance calculations yield the largest minimum flux and are hence the most realistic. 相似文献
2.
河南栾川地区是我国著名斑岩钼矿集区,近年铅锌矿勘查取得重要进展,但对铅锌矿成因认识分歧颇多。研究表明,栾川地区铅锌矿产在燕山期斑岩钼矿床外围,矿区地层为中元古界官道口群和新元古界栾川群碳酸盐岩-碎屑岩沉积变质建造,地层中侵入有晋宁期辉长岩、正长岩和燕山期酸性斑岩,铅锌矿呈脉状或透镜状,发育3种类型:受燕山期斑岩与元古界钙质地层接触带控制的夕卡岩型铅锌矿、受北西西向层间断裂构造控制的脉状铅锌矿和受北东或近南北向张-张扭性断裂控制的脉状铅锌矿。铅锌矿石中硫化物δ~(34)S_(V-CDT)为近零的正值(骆驼山0.37‰～4.20‰、赤土店-0.32‰～8.30‰、百炉沟-1.20‰～10.90‰、冷水北沟0.70‰～12.10‰),岩浆来源硫特征明显;夕卡岩型铅锌硫化物的δ~(34)S_(V-CDT)与本地斑岩型钼矿石中硫化物的δ~(34)S_(V-CDT)(1.24‰～3.30‰)极为相近,脉状铅锌硫化物的δ~(34)S_(V-CDT)与斑岩型钼矿石中硫化物重合,但有地层中硫(δ~(34)S_(V-CDT)为12.43‰～18.63‰)的影响。总体上δ~(34)S_(黄铁矿)>δ~(34)S_(闪锌矿)>δ~(34)S_(方铅矿),指示矿石中主要硫化物矿物硫同位素分馏基本达到平衡,赤土店铅锌矿石中共生方铅矿与闪锌矿的硫同位素温度计指示硫化物矿物沉淀温度较高(388.29℃)。河南栾川地区铅锌矿主体应为受燕山期构造-岩浆作用控制的中高温热液铅锌矿床。 相似文献
3.
Multiple isotope composition (S, Pb, H, O, He, and Ar) and genetic implications for gold deposits in the Jiapigou gold belt, Northeast China 总被引：2，自引：0，他引：2
Qingdong Zeng Zaicong Wang Huaiyu He Yongbin Wang Song Zhang Jianming Liu 《Mineralium Deposita》2014,49(1):145-164
The Jiapigou gold belt (>150 t Au), one of the most important gold-producing districts in China, is located at the northeastern margin of the North China Craton. It is composed of 17 gold deposits with an average grade around 10 g/t Au. The deposits are hosted in Archean gneiss and TTG rocks, and are all in shear zones or fractures of varying orientations and magnitudes. The δ34S values of sulfide from ores are mainly between 2.7?‰ and 10?‰. The Pb isotope characteristics of ore sulfides are different from those of the Archean metamorphic rocks and Mesozoic granites and dikes, and indicate that they have different lead sources. The sulfur and lead isotope compositions imply that the ore-forming materials might originate from multiple, mainly deep sources. Fluid inclusions in pyrite have 3He/4He ratios of 0.6 to 2.5 Ra, whereas their 40Ar/36Ar ratios range from 1,444 to 9,805, indicating a dominantly mantle fluid with a negligible crustal component. δ18O values calculated from hydrothermal quartz are between ?0.2?‰ and +5.9?‰, and δD values of the fluids in the fluid inclusions in quartz are from ?70?‰ to ?96?‰. These ranges suggest dominantly magmatic water with a minor meteoric component. The noble gas isotopic data, along with the stable isotopic data, suggest that the ore-forming fluids have a dominantly mantle source with minor crustal addition. 相似文献
4.
The Himalayan mineral field includes over 50 quartz-vein type Sb-Au deposits, and placer Au deposits. The poorly documented Laqiong deposit is a typical example of quartz-vein type Sb-Au mineralisation in Tethys Himalayan sequence. The orebody are controlled by shallow north-dipping normal faults and north–south trending faults. Magmatic zircons extracted from muscovitic leucocratic granite from the southern part of the Laqiong mine area yield a Laser Ablation-Inductively Coupled Plasma-Mass Spectrometry U-Pb age of 14 ± 1 Ma (n = 12, MSWD = 0.9) that is similar to the 40Ar/39Ar age of ca. 14 Ma from hydrothermal sericite in auriferous sulphide-quartz veins. The εHf(t) values for the magmatic zircon rims range from −5.4 to −1.9, corresponding to two-stage Hf model ages of 1403–1214 Ma. Quartz from the mineralised veins has δ18OH2O-SMOW values varying from +4.97 to +9.59‰ and δDH2O-SMOW values ranging from −119.7 to −108.1‰. The δ13CV-PDB values for calcite from the ore Stage III range from −6.9 to −5.3‰, and calcite from Stage IV are −3.5 to −1.7‰. The δ18OV-SMOW values for calcite from Stage III are +20.3 to +20.6‰ and for Stage IV are −6.3 to −4.9‰. The stibnite and pyrite samples have 208Pb/204Pb ratios of 38.158 to 39.02, 207Pb/204Pb ratios of 15.554 to 15.698, and 206Pb/204Pb ratios of 17.819 to 18.681, and bulk and in-situ δ34SV-CDT values for stibnite, arsenopyrite and pyrite range from −1.1 to +2.3‰. The calcite from the orebodies are enriched in MREE and depleted in LREE and HREE. Fieldwork, petrological, and geochemical data collected during our study leads to the following salient findings: the mineralising fluid is a mix of magmatic and meteoric fluids; and the deposit is closely related to the emplacement of Miocene granites originating from a thickened continental crust. 相似文献
5.
Qingdong Zeng Jianming Liu Tiebing Liu Yuanchao Shen Ping Shen Guangming Li 《Resource Geology》2007,57(3):313-324
The Sawuershan region, one of the important gold metallogenic belts of Xinjiang, is located in the western part of the Kalatongke island arc zone of north Xinjiang, NW China. There are two gold deposits in mining, namely the Kuoerzhenkuola and the Buerkesidai deposits. Gold ores at the Kuoerzhenkuola deposit occur within Carboniferous andesite and volcanic breccias in the form of gold‐bearing quartz–pyrite veins and veinlet groups containing native gold, electrum, pyrite, pyrrhotite and chalcopyrite. Gold ores at the Buerkesidai deposit occur within Carboniferous tuffaceous siltstones in the form of gold‐bearing quartz veinlet groups and altered rocks, with electrum, pyrite and arsenopyrite as major metallic minerals. Both gold deposits are hosted by structurally controlled faults associated with intense hydrothermal alteration. The typical alteration assemblage is sericite + chlorite + calcite + quartz, with an inner pyrite–sericite zone and an outer chlorite–calcite–epidote zone between orebodies and wall rocks. δ34S values (0.3–1.3‰) of pyrite of ores from Kuoerzhenkuola deposit are similar to those (0.4–2.9‰) of pyrite of ores from Buerkesidai deposit. δ34S values (1.1–2.8‰) of pyrite from altered rocks are similar to δ34S values of magmatic or igneous sulfide sulfur, but higher than those from ores. 206Pb/204Pb, 207Pb/204Pb and 208Pb/204Pb data of sulfide from ores range within 17.72–18.56, 15.34–15.61, and 37.21–38.28, respectively. These sulfur and lead isotope compositions imply that ore‐forming materials might originate from multiple, mainly deep sources. He and Ar isotope study on fluid inclusions of pyrites from ores of Kuoerzhenkuola and Buerkesidai gold deposits produces 40Ar/36Ar and 3He/4He ratios in the range of 282–525 and 0.6–9.4 R/Ra, respectively, indicating a mixed source of deep‐seated magmatic water (mantle fluid) and shallower meteoric water. In terms of tectonic setting, the gold deposits in the Sawuershan region can be interpreted as epithermal. These formations resulted from a combination of protracted volcanic activity, hydrothermal fluid mixing, and a structural setting favoring gold deposition. Fluid mixing was possibly the key factor resulting in Au deposition in the gold deposits in Sawuershan region. 相似文献
6.
Copper and iron skarn deposits are economically important types of skarn deposits throughout the world, especially in China, but the differences between Cu and Fe skarn deposits are poorly constrained. The Edong ore district in southeastern Hubei Province, Middle–Lower Yangtze River metallogenic belt, China, contains numerous Fe and Cu–Fe skarn deposits. In this contribution, variations in skarn mineralogy, mineralization-related intrusions and sulfur isotope values between these Cu–Fe and Fe skarn deposits are discussed.The garnets and pyroxenes of the Cu–Fe and Fe skarn deposits in the Edong ore district share similar compositions, i.e., dominantly andradite (Ad29–100Gr0–68) and diopside (Di54–100Hd0–38), respectively. This feature indicates that the mineral compositions of skarn silicate mineral assemblages were not the critical controlling factors for variations between the Cu–Fe and Fe skarn deposits. Intrusions associated with skarn Fe deposits in the Edong ore district differ from those Cu–Fe skarn deposits in petrology, geochemistry and Sr–Nd isotope. Intrusions associated with Fe deposits have large variations in their (La/Yb)N ratios (3.84–24.6) and Eu anomalies (δEu = 0.32–1.65), and have relatively low Sr/Y ratios (4.2–44.0) and high Yb contents (1.20–11.8 ppm), as well as radiogenic Sr–Nd isotopes (εNd(t) = − 12.5 to − 9.2) and (87Sr/86Sr)i = 0.7067 to 0.7086. In contrast, intrusions associated with Cu–Fe deposits are characterized by relatively high Sr/Y (35.0–81.3) and (La/Yb)N (15.0–31.6) ratios, low Yb contents (1.00–1.62 ppm) without obvious Eu anomalies (δEu = 0.67–0.97), as well as (87Sr/86Sr)i = 0.7055 to 0.7068 and εNd(t) = − 7.9 to − 3.4. Geochemical evidence indicates a greater contribution from the crust in intrusions associated with Fe skarn deposits than in intrusions associated with Cu–Fe skarn deposits. In the Edong ore district, the sulfides and sulfates in the Cu–Fe skarn deposits have sulfur isotope signatures that differ from those of Fe skarn deposits. The Cu–Fe skarn deposits have a narrow range of δ34S values from − 6.2‰ to + 8.7‰ in sulfides, and + 13.2‰ to + 15.2‰ in anhydrite, while the Fe skarn deposits have a wide range of δ34S values from + 10.3‰ to + 20.0‰ in pyrite and + 18.9‰ to + 30.8‰ in anhydrite. Sulfur isotope data for anhydrite and sedimentary country rocks suggest that the formation of skarns in the Edong district involved the interaction between magmatic fluids and variable amounts of evaporites in host rocks. 相似文献
7.
The Cangyuan Pb-Zn-Ag polymetallic deposit is located in the Baoshan Block, southern Sanjiang Orogen. The orebodies are hosted in low-grade metamorphic rocks and skarn in contact with Cenozoic granitic rocks. Studies on fluid inclusions (FIs) of the deposit indicate that the ore-forming fluids are CO2-bearing, NaCl-H2O. The initial fluids evolved from high temperatures (462–498 °C) and high salinities (54.5–58.4 wt% NaCl equiv) during the skarn stage into mesothermal (260–397 °C) and low salinities (1.2–9.5 wt% NaCl equiv) during the sulfide stage. The oxygen and hydrogen isotopic compositions (δ18OH2O: 2.7–8.8‰; δD: −82 to −120‰) suggest that the ore-forming fluids are mixture of magmatic fluids and meteoric water. Sulfur isotopic compositions of the sulfides yield δ34S values of −2.3 to 3.2‰; lead isotopic compositions of ore sulfides are similar to those of granitic rocks, indicating that the sulfur and ore-metals are derived from the granitic magma. We propose that the Cangyuan Pb-Zn-Ag deposit formed from magmatic hydrothermal fluids. These Cenozoic deposits situated in the west of Lanping-Changdu Basin share many similarities with the Cangyuan in isotopic compositions, including the Laochang, Lanuoma and Jinman deposits. This reveals that the Cenozoic granites could have contributed to Pb-Zn-Cu mineralization in the Sanjiang region despite the abundance of Cenozoic Pb-Zn deposits in the region, such as the Jingding Pb-Zn deposit, that is thought to be of basin brine origin. 相似文献
8.
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
9.
《International Geology Review》2012,54(10):920-943
The Bajiazi deposits of western Liaoning Province, northeastern China, are aligned approximately west-east in an 8-× 15-km district. The Zn-Pb-Ag-FeS2 sulfide ores are hosted in intensively folded and faulted Early Proterozoic carbonates and minor clastic rocks, near their contact with Late Jurassic-Early Cretaceous Bajiazi granite. The ore-bearing strata on both limbs of the Bajiazi syncline can be correlated throughout the district. Orebodies are stratigraphically conformable with the host rocks and mostly parallel the contact metamorphic halo of the granite, in the skarn mineralizing zone. The ores are composed of stratabound and stratiform sulfide lenses and layers, are associated with sediments formed in local depressions of a tectonically active, shallow-marine environment, and are limited to dolomitized tidal flat and lagoonal facies with cryptalgal lamination and to adjacent oolitic grainstones of barrier facies. The ores consist of fine- to medium-grained intergrowths of sulfides in dolomite and locally skarn gangues. Sulfides are intensely recrystallized and annealed in the contact metamorphic halo. Isotopes of sulfur, carbon, oxygen, and lead were examined for genetic interpretation of the sulfides and host rocks. Sulfur isotope values range from ?9.1 to 13.0 per mil for sulfides, suggesting sedimentary exhalative origin, though they were, to some extent, homogenized during late overprinting events. The δ18O values range between ?6 and ?15 per mil PDB, and the δ13C values between +1 and ?5 per mil PDB. Late crystallization generations are enriched in the light isotopes of oxygen and carbon compared to primary ones. Lead isotope ratios in galenas from all Bajiazi ores have means of 206Pb/204Pb = 16.23, 207Pb/204Pb = 15.23, and 208Pb/204Pb = 36.51. These isotope ratios, characterized by a model age of about 1350 Ma, suggest an early Proterozoic, crustal source for the lead in the ores, unrelated to the lead in the Mesozoic granite. All evidence identified in this study suggests that the Bajiazi polymetallic sulfide deposits formed as sedimentary exhalative accumulations in a Lower Proterozoic, shallow-marine sedimentary basin. The present distribution of the ores and their distinctive textures indicate overprinting by. contemporaneous and/or post-depositional tectonic processes, as well as contact metamorphism during the emplacement of the Mesozoic Bajiazi granite. 相似文献
10.
V.V. Ryabov O.N. Simonov S.G. Snisar A.A. Borovikov 《Russian Geology and Geophysics》2018,59(8):945-961
The source of sulfur in giant Norilsk-type sulfide deposits is discussed. A review of the state of the problem and a critical analysis of existing hypotheses are made. The distribution of δ34S in sulfides of ore occurrences and small and large deposits and in normal sedimentary, metamorphogenic, and hypogene sulfates is considered. A large number of new δ34S data for sulfides and sulfates in various deposits, volcanic and terrigenous rocks, coals, graphites, and metasomatites are presented. The main attention is focused on the objects of the Norilsk and Kureika ore districts. The δ34S value varies from -14 to + 22.5‰ in sulfides of rocks and ores and from 15.3 to 33‰ in anhydrites. In sulfide-sulfate intergrowths and assemblages, δ34S is within 4.2-14.6‰ in sulfides and within 15.3-21.3‰ in anhydrites. The most isotopically heavy sulfur was found in pyrrhotite veins in basalts (δ34S = 21.6‰), in sulfate veins cutting dolomites (δ34S = 33‰), and in subsidence caldera sulfates in basalts (δ34S = 23.2-25.2‰). Sulfide ores of the Tsentral’naya Shilki intrusion have a heavy sulfur isotope composition (δ34S = + 17.7‰ (n = 15)). Thermobarogeochemical studies of anhydrites have revealed inclusions of different types with homogenization temperatures ranging from 685 °C to 80 °C. Metamorphogenic and hypogene anhydrites are associated with a carbonaceous substance, and hypogene anhydrites have inclusions of chloride-containing salt melts. We assume that sulfur in the trap sulfide deposits was introduced with sulfates of sedimentary rocks (δ34S = 22-24‰). No assimilation of sulfates by basaltic melt took place. The sedimentary anhydrites were “steamed” by hydrocarbons, which led to sulfate reduction and δ34S fractionation. As a result, isotopically light sulfur accumulated in sulfides and hydrogen sulfide, isotopically heavy sulfur was removed by aqueous calcium sulfate solution, and “residual” metamorphogenic anhydrite acquired a lighter sulfur isotope composition as compared with the sedimentary one. The wide variations in δ34S in sulfides and sulfates are due to changes in the physicochemical parameters of the ore-forming system (first of all, temperature and Pch4) during the sulfate reduction. The regional hydrocarbon resources were sufficient for large-scale ore formation. 相似文献
11.
Abstract: Crystalline limestone of the Sako-nishi area in the Kamioka Zn-Pb mine, central Japan, is depleted in 18O and 13C toward the center of mineralization due to interaction with hydrothermal fluids with a dominant meteoric water component. The relationship between isotopic composition and mineral assemblage, texture, the chemical composition of the minerals, and the bulk chemical composition in the limestone was examined. A decrease in the δ18OSMOW value correlated with: (1) increase of fine-grained calcite which is enriched in Mn and exhibits a bright cathodoluminescence, (2) progressive hy-drothermal alteration of clinopyroxene in the original limestone into tremolite within the weakly-altered zone, and into chlorite and actinolite within the strongly-altered zone, (3) dominance of hydrothermal chlorite in altered limestone having δ18O values of less than 10%. This chlorite was enriched in Fe compared to mafic minerals in the unaltered limestone. The enrichment of Fe and Mn was more conspicuous in calcite and chlorite in skarn deposits. The occurrence and chemical composition of hydrothermal minerals in the limestone, skarn, and ore indicate that the 18O–depleted zones were formed in the later stage from fluids, which were responsible for mineralization and skarnization, and for Fe and Mn enrichment. The Al, Mn, and Fe contents, and the ratios of Mg/(Mg+Mn+Fe), Al/Mg, and Mn/Sr in the hydrochloric acid leachate of limestone varied with decreasing δ18O and δ13C values, reflecting increases in high-Mn calcite and high-Fe chlorite. These indexes were useful for the identification of hydrothermally altered limestone. Furthermore, the potential score weighted by each index was more effective and accurate means of detecting promising mineralization zones. An anomalous potential score due to the presence of hydrothermal minerals in the outcropping limestone occurred along the Atotsu–1GO fault. This structure indicates that the skarn deposits of the Sako-nishi area belong to Mozumi-type Zn–Pb skarn deposits, in which fissures and faults served as major passages for the hydrothermal fluid. High-Mn carbonate and high-Fe chlorite widely occur in base-metal vein deposits and Zn-Pb type skarn deposits. Leaching of altered rock with hydrochloric acid in addition to stable isotope composition and cathodoluminescence imaging is effective for geochemical exploration for hydrothermal deposits because it makes possible the detection of the elemental composition of hydrothermal minerals such as chlorite and carbonate and because of the rapidity and convenience of analysis. 相似文献
12.
老挝班康姆矿床是近年来在琅勃拉邦-黎府成矿带新发现的一个大型铜金矿床。该矿床矽卡岩与矿体主要赋存在安山岩中且缺乏矽卡岩分带,与典型矽卡岩矿床的地质特征存在一定的差别。因此,厘清班康姆铜金矿床的成矿流体、成矿物质来源及矿床成因机制是后续开展琅勃拉邦-黎府成矿带大型铜金矿床找矿勘探的基础。该矿床矿化阶段石英流体包裹体δD分布于-110‰~-90‰,δ18O分布于-1.5‰~7.1‰,其中低δD的样品具有相对高的δ18O值;黄铁矿流体包裹体的3He/4He为0.41~3.43Ra(大部分<1Ra),40Ar/36Ar为314.8~362.4。H-O及He-Ar同位素结果表明,班康姆矿床成矿流体来源于岩浆流体(至少部分来自地幔)与低δD的大气雨水的混合,雨水占更大的比例,且某些矿化流体的雨水端元在混合前经历了明显的水岩作用。除一件样品(BK64)的黄铁矿具有高的δ34S(8.1‰)外,其余硫化物的δ34S分布于-0.9‰~1.5‰,位于地幔硫的范围。共生硫化物对的硫同位素平衡分馏计算以及动力学分馏不支持高δ34S(8.1‰)黄铁矿的硫来自从热液流体,可能来自围岩。热液方解石的δ13C范围为-3.1‰~2.5‰,δ18O变化于26.0‰~28.4‰,指示其碳来自矿区灰岩,而灰岩的溶解为热液摄取围岩的重硫提供了可能。矿石黄铁矿Pb同位素组成(206Pb/204Pb:17.9284~18.7756;207Pb/204Pb:15.5336~15.6651;208Pb/204Pb:37.9125~38.8090)位于黎府褶皱带和长山褶皱带晚二叠世—中三叠世大陆弧岩浆岩的Pb同位素范围,介于印支地块玄武岩和泰国-老挝S-型花岗岩及相关矿床的Pb同位素组成之间,指示班康姆矿床的Pb来自壳幔混合源。本文S-Pb-He-Ar同位素结果及区域Cu-Au成矿过程的岩石地化研究,表明班康姆矿床Cu、Au主要来自地幔。与典型矽卡岩Cu-Au矿床的S-Pb-H-O同位素及矽卡岩矿物流体包裹体盐度特征的对比,结合前人的火山气热液交代火山岩形成矽卡岩的实验结果,认为班康姆矽卡岩型Cu-Au矿床的形成机制为深部出溶的气相为主的含矿岩浆流体沿断裂上升到浅部交代安山岩或大理岩并经历了流体混合、沸腾及矿石沉淀等过程。 相似文献
13.
DING Hui GE Wensheng DONG Lianhui ZHANG Liangliang CHEN Xiaodong LIU Yan NIE Junjie 《《地质学报》英文版》2018,92(3):1100-1122
The Weiquan Ag-polymetallic deposit is located on the southern margin of the Central Asian Orogenic Belt and in the western segment of the Aqishan-Yamansu arc belt in East Tianshan,northwestern China. Its orebodies, controlled by faults, occur in the lower Carboniferous volcanosedimentary rocks of the Yamansu Formation as irregular veins and lenses. Four stages of mineralization have been recognized on the basis of mineral assemblages, ore fabrics, and crosscutting relationships among the ore veins. Stage I is the skarn stage(garnet + pyroxene), Stage Ⅱ is the retrograde alteration stage(epidote + chlorite + magnetite ± hematite 士 actinolite ± quartz),Stage Ⅲ is the sulfide stage(Ag and Bi minerals + pyrite + chalcopyrite + galena + sphalerite + quartz ± calcite ± tetrahedrite),and Stage IV is the carbonate stage(quartz + calcite ± pyrite). Skarnization,silicification, carbonatization,epidotization,chloritization, sericitization, and actinolitization are the principal types of hydrothermal alteration. LAICP-MS U-Pb dating yielded ages of 326.5±4.5 and 298.5±1.5 Ma for zircons from the tuff and diorite porphyry, respectively. Given that the tuff is wall rock and that the orebodies are cut by a late diorite porphyry dike, the ages of the tuff and the diorite porphyry provide lower and upper time limits on the age of ore formation. The δ~(13)C values of the calcite samples range from-2.5‰ to 2.3‰, the δ~(18)O_(H2 O) and δD_(VSMOW) values of the sulfide stage(Stage Ⅲ) vary from 1.1‰ to 5.2‰ and-111.7‰ to-66.1‰, respectively,and the δ~(13)C, δ~(18)O_(H2 O) and δD_(V-SMOW) values of calcite in one Stage IV sample are 1.5‰,-0.3‰, and-115.6‰, respectively. Carbon, hydrogen, and oxygen isotopic compositions indicate that the ore-forming fluids evolved gradually from magmatic to meteoric sources. The δ~(34)S_(V-CDT) values of the sulfides have a large range from-6.9‰ to 1.4‰, with an average of-2.2‰, indicating a magmatic source, possibly with sedimentary contributions. The ~(206)Pb/~(204)Pb, ~(207)Pb/~(204)Pb, and ~(208)Pb/~(204)Pb ratios of the sulfides are 17.9848-18.2785,15.5188-15.6536, and 37.8125-38.4650, respectively, and one whole-rock sample at Weiquan yields~(206)Pb/~(204)Pb,~(207)Pb/~(204)Pb, and ~(208)Pb/~(204)Pb ratios of 18.2060, 15.5674, and 38.0511,respectively. Lead isotopic systems suggest that the ore-forming materials of the Weiquan deposit were derived from a mixed source involving mantle and crustal components. Based on geological features, zircon U-Pb dating, and C-H-OS-Pb isotopic data, it can be concluded that the Weiquan polymetallic deposit is a skarn type that formed in a tectonic setting spanning a period from subduction to post-collision. The ore materials were sourced from magmatic ore-forming fluids that mixed with components derived from host rocks during their ascent, and a gradual mixing with meteoric water took place in the later stages. 相似文献
14.
The Paleozoic Ozbak-Kuh carbonate-hosted Pb-Zn deposit of East Central Iran: Isotope (C,O, S,Pb) geochemistry and ore genesis 总被引：1，自引：0，他引：1
Farhad Ehya 《Mineralogy and Petrology》2014,108(1):123-136
Lead and zinc mineralization occurs in dolostones of the Middle Devonian Sibzar Formation at Ozbak-Kuh, which is located 150 km north of Tabas city in East Central Iran. The ore is composed of galena, sphalerite and calcite, with subordinate dolomite and bitumen. Wall-rock alterations include carbonate recrystallization and dolomitization. Microscopic studies reveal that the host rock is replaced by galena and sphalerite. The Pb–Zn mineralization is epigenetic and stratabound. The δ13C values of hydrothermal calcite samples fall in the narrow range between ?0.3‰ and 0.8‰. The δ18O values in calcite display a wider range, between ?14.5‰ and ?11.9‰. The δ13C and δ18O values overlap with the oxygen and carbon isotopic compositions of Paleozoic seawater, indicating the possible important participation of Paleozoic seawater in the ore-forming fluid. The δ18O signature corresponds to a spread in temperature of about 70 °C in the ore-bearing fluid. The δ13C values indicate that the organic materials within the host rocks did not contribute significantly in the hydrothermal fluid. The δ34S values of galena and sphalerite samples occupy the ranges of 12.2‰–16.0‰ and 12.1–16.8‰, respectively. These values reveal that the seawater sulfate is the most probable source of sulfur. The reduced sulfur was most likely supplied through thermochemical sulfate reduction. The sulfur isotope ratios of co-precipitated sphalerite–galena pairs suggest that deposition of the sulfide minerals took place under chemical disequilibrium conditions. The 206Pb/204Pb, 207Pb/204Pb, and 208Pb/204Pb ratios of the galena samples represent average values of 18.08, 15.66, and 38.50, respectively. These ratios indicate that galena Pb likely originated from an orogenic source in which supracrustal rocks with high 238U/204Pb and 232Th/204Pb ratios are dominant. The average lead isotope model age portrays Cambrian age. This model age is not coeval with the host rocks, which are of middle Devonian age. It is probable that the pre-Middle Devonian model age shows the derivation of Pb from older sources either from host rocks of Cambrian age or from deposits previously formed in these rock units. The Pb isotopic composition of galena accords with the occurrence of an orogenic activity from Late Neoproterozoic to Lower Cambrian in Central Iran. The proposed genetic model considers the fact that mineralization formed in fractured and brecciated host rocks along shear zones and faults from metal-bearing connate waters that were discharged due to deformational dewatering of sediments. 相似文献
15.
Lei CHEN Kezhang QIN Jinxiang LI Bo XIAO Guangming LI Junxing ZHAO Xin FAN 《Resource Geology》2012,62(1):42-62
The Nuri Cu‐W‐Mo deposit is located in the southern subzone of the Cenozoic Gangdese Cu‐Mo metallogenic belt. The intrusive rocks exposed in the Nuri ore district consist of quartz diorite, granodiorite, monzogranite, granite porphyry, quartz diorite porphyrite and granodiorite porphyry, all of which intrude in the Cretaceous strata of the Bima Group. Owing to the intense metasomatism and hydrothermal alteration, carbonate rocks of the Bima Group form stratiform skarn and hornfels. The mineralization at the Nuri deposit is dominated by skarn, quartz vein and porphyry type. Ore minerals are chalcopyrite, pyrite, molybdenite, scheelite, bornite and tetrahedrite, etc. The oxidized orebodies contain malachite and covellite on the surface. The mineralization of the Nuri deposit is divided into skarn stage, retrograde stage, oxide stage, quartz‐polymetallic sulfide stage and quartz‐carbonate stage. Detailed petrographic observation on the fluid inclusions in garnet, scheelite and quartz from the different stages shows that there are four types of primary fluid inclusions: two‐phase aqueous inclusions, daughter mineral‐bearing multiphase inclusions, CO2‐rich inclusions and single‐phase inclusions. The homogenization temperature of the fluid inclusions are 280°C–386°C (skarn stage), 200°C–340°C (oxide stage), 140°C–375°C (quartz‐polymetallic sulfide stage) and 160°C–280°C (quartz‐carbonate stage), showing a temperature decreasing trend from the skarn stage to the quartz‐carbonate stage. The salinity of the corresponding stages are 2.9%–49.7 wt% (NaCl) equiv., 2.1%–7.2 wt% (NaCl) equiv., 2.6%–55.8 wt% (NaCl) equiv. and 1.2%–15.3 wt% (NaCl) equiv., respectively. The analyses of CO2‐rich inclusions suggest that the ore‐forming pressures are 22.1 M Pa–50.4 M Pa, corresponding to the depth of 0.9 km–2.2 km. The Laser Raman spectrum of the inclusions shows the fluid compositions are dominated in H2O, with some CO2 and very little CH4, N2, etc. δD values of garnet are between ?114.4‰ and ?108.7‰ and δ18OH2O between 5.9‰ and 6.7‰; δD of scheelite range from ?103.2‰ to ?101.29‰ and δ18OH2O values between 2.17‰ and 4.09‰; δD of quartz between ?110.2‰ and ?92.5‰ and δ18OH2O between ?3.5‰ and 4.3‰. The results indicate that the fluid came from a deep magmatic hydrothermal system, and the proportion of meteoric water increased during the migration of original fluid. The δ34S values of sulfides, concentrated in a rage between ?0.32‰ to 2.5‰, show that the sulfur has a homogeneous source with characteristics of magmatic sulfur. The characters of fluid inclusions, combined with hydrogen‐oxygen and sulfur isotopes data, show that the ore‐forming fluids of the Nuri deposit formed by a relatively high temperature, high salinity fluid originated from magma, which mixed with low temperature, low salinity meteoric water during the evolution. The fluid flow through wall carbonate rocks resulted in the formation of layered skarn and generated CO2 or other gases. During the reaction, the ore‐forming fluid boiled and produced fractures when the pressure exceeded the overburden pressure. Themeteoric water mixed with the ore‐forming fluid along the fractures. The boiling changed the pressure and temperature, oxygen fugacity, physical and chemical conditions of the whole mineralization system. The escape of CO2 from the fluid by boiling resulted in scheelite precipitation. The fluid mixing and boiling reduced the solubility of metal sulfides and led the precipitation of chalcopyrite, molybdenite, pyrite and other sulfide. 相似文献
16.
黑龙江省双鸭山市羊鼻山铁钨矿床处于中亚造山带东段的佳木斯地块中部。兴东群大盘道组变质岩系为矿区主要赋矿地层,铁矿矿体呈层状、似层状赋存于大盘道组第一岩段,白钨矿矿体呈透镜状和脉状产于铁矿矿体底板围岩中,受片麻状花岗岩与大盘道组大理岩的接触带控制;主要含矿岩石为石榴石矽卡岩和透辉石矽卡岩,钨矿石中主要金属矿物为磁黄铁矿和白钨矿,并含少量磁铁矿、黄铁矿、黄铜矿、闪锌矿、锡石、毒砂和辉钼矿。含钨石英脉中δ18O水值为3.6‰~7.5‰,δD值为-120.9‰~-66.2‰,表明其成矿流体以岩浆水为主。矽卡岩中与白钨矿共生的金属硫化物δ34S值为16.1‰~18.1‰,206Pb/204Pb值为17.879~18.863,207Pb/204Pb值为15.537~15.603,208Pb/204Pb值为38.202~38.544,表明金属硫化物中的硫和铅主要来源于地层与地壳重熔型岩浆。结合钨矿成矿地质特征,认为羊鼻山铁钨矿床中钨矿的成因类型应属矽卡岩型。 相似文献
17.
More than 200 analyses of the sulfur isotopic composition of sulfides from various terrigenous and intrusive host rocks, metasomatically altered wall rocks, and gold lodes of the Upper Kolyma region are presented. In accessory pyrite of the metaterrigenous rocks, δ34S varies from ?23.1 to +5.7‰ δ34S of pyrite and arsenopyrite from gold-quartz mineralization is within the range ?10.6 to ?0.4‰ and is close to the average δ34S of pyrite from the metaterrigenous rocks (?4.4‰). In the intrusive rocks, δ34S of pyrite varies from ?3.8 to +2.6‰ (+0.7‰, on average) and drastically differs from δ34S of arsenopyrite from postmagmatic gold-rare-metal mineralization (?7.9 to ?2.7‰; ?5.2‰, on average). The comparison of the δ34S of accessory sulfides from the host rocks with δ34S of sulfides from the gold deposits suggests that sulfur mobilized from the terrigenous sequences participated in the hydrothermal process. The results obtained are consistent with the metamorphic model of the formation of gold-quartz deposits in the Upper Kolyma region. 相似文献
18.
The Huangshilao gold deposit (>13.5 t Au) is comprised of stratabound pyrite‐dominant massive sulfide ores, and is distinguished from the skarn Cu, Au, and Cu–Au deposits that are dominant in the Tongguanshan orefield, Tongling, east‐central China. The stratabound orebodies are situated along flexural slip faults along the unconformity between the Upper Devonian Wutong and the Upper Carboniferous Huanglong Formations. The ores, dominated by crystallized pyrite, colloform pyrite, and pyrrhotite, are systematically sampled from the underground stopes along strike drifts. The δ34S values of ore sulfides yield a wide variation from ?11.3 to 11.4‰, but mostly within 4–8‰, corresponding to the δ34S range (3.4–8.7‰) of the Yanshanian Tongguanshan and Tianshan quartz diorite intrusions in the Tongguanshan orefield, suggesting a magmatic dominated sulfur source. Few obvious negative δ34S values are induced by an involvement of sedimentation‐related biogenic sulfur. The wide δ34S variation denotes an incongruent physical and chemical interaction of the two sources. Combined analysis of gold contents and sulfur isotopes of the sulfides show that the magmatic hydrothermal solution provides primary metals despite a small quantity that may have been contributed by the sedimentary pyrites. The hydrothermal alteration, thermal metamorphism, trace element concentration in pyrites, and existing aeromagnetic data jointly suggest that the hydrothermal fluid migrated vertically from an intrusion below, along the flexural slip faults, but not laterally from the nearby outcrop of Tianshan stock. 相似文献
19.
Exploration of Zn-rich sulphide deposits at Leadville, northern Lachlan Fold Belt, New South Wales, for over two decades has been largely on the premise that the mineralisation represents felsic volcanic-hosted massive sulphides (VHMS). Deposits are hosted by ?Silurian felsic metavolcanic, psammopelitic and calcareous metasedimentary rocks which have been intruded by the late Carboniferous I-type Gulgong Granite. Evidence for an epigenetic replacement (skarn) origin of the deposits, rather than representing metamorphosed volcanogenic massive sulphides, includes the proximity of evolved granitic intrusives and reactive carbonate rocks, a skarn mineral assemblage (with characteristic prograde and retrograde stages), lack of textural or lithological indications of an exhalative origin, and gossan and sulphide compositions consistent with Zn-Pb skarns and atypical of Lachlan Fold Belt VHMS deposits. Furthermore, sulphide lead isotope ratios are significantly more radiogenic than signatures for VHMS deposits in the Lachlan Fold Belt. Carbonate δ13C and δ18O and sulphide δ34S values are consistent with the interaction of magmatic hydrothermal fluids with Palaeozoic carbonate rocks and a largely magmatic source of sulphur. It is concluded that the Leadville deposits are of skarn type, genetically related to the Gulgong Granite. 相似文献
20.
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