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1.
The Maoduan Pb–Zn–Mo deposit is in hydrothermal veins with a pyrrhotite stage followed by a molybdenite and base metal stage. The Re–Os model ages of five molybdenite samples range from 138.6 ± 2.0 to 140.0 ± 1.9 Ma. Their isochron age is 137.7 ± 2.7 Ma. Laser ablation inductively coupled plasma mass spectrometry (LA-ICP-MS) zircon U–Pb dating of the nearby exposed Linggen granite porphyry gave a 206Pb/238U age of 152.2 ± 2.2 Ma and the hidden Maoduan monzogranite yielded a mean of 140.0 ± 1.6 Ma. These results suggest that the intrusion of the Maoduan monzogranite and Pb–Zn–Mo mineralization are contemporaneous. δ 34S values of sulfide minerals range from 3.4‰ to 4.8‰, similar to magmatic sulfur. Four sulfide samples have 206Pb/204Pb = 18.252–18.432, 207Pb/204Pb = 15.609–15.779, and 208Pb/204Pb = 38.640–39.431, similar to the age-corrected data of the Maoduan monzogranite. These isotope data support a genetic relationship between the Pb–Zn–Mo mineralization and the Maoduan monzogranite and probably indicate a common deep source. The Maoduan monzogranite has geochemical features similar to highly fractionated I-type granites, such as high SiO2 (73.7–75.2 wt.%) and alkalis (K2O + Na2O = 7.8–8.9 wt.%) and low FeOt (0.8–1.3 wt.%), MgO (~0.3 wt.%), P2O5 (~0.03 wt.%), and TiO2 (~0.2 wt.%). The granitic rocks are enriched in Rb, Th, and U but depleted in Ba, Sr, Nb, Ta, P, and Ti. REE patterns are characterized by marked negative Eu anomalies (Eu/Eu* = 0.2–0.4). The Maoduan monzogranite, having (87Sr/86Sr) t  = 0.7169 to 0.7170 and εNd(t) = −13.8 to −13.7, was probably derived from mixing of partial melts from enriched mantle and the Paleoproterozoic Badu group in an extensional tectonic setting.  相似文献   

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The Wittichen Co–Ag–Bi–U mining area (Schwarzwald ore district, SW Germany) hosts several unconformity-related vein-type mineralizations within Variscan leucogranite and Permian to Triassic redbeds. The multistage mineralization formed at the intersection of two fault systems in the last 250 Ma. A Permo-Triassic ore stage I with minor U–Bi–quartz–fluorite mineralization is followed by a Jurassic to Cretaceous ore stage II with the main Ag and Co mineralization consisting of several generations of gangue minerals that host the sub-stages of U–Bi, Bi–Ag, Ni–As–Bi and Co–As–Bi. Important ore minerals are native elements, Co and Ni arsenides, and pitchblende; sulphides are absent. The Miocene ore stage III comprises barite with the Cu–Bi sulfosalts emplectite, wittichenite and aikinite, and the sulphides anilite and djurleite besides native Bi, chalcopyrite, sphalerite, galena and tennantite. The mineral-forming fluid system changed from low salinity (<5 wt.% NaCl) at high temperature (around 300°C) in Permian to highly saline (around 25 wt.% NaCl + CaCl2) at lower temperatures (50–150°C) in Triassic to Cretaceous times. Thermodynamic calculations and comparison with similar mineralizations worldwide show that the Mesozoic ore-forming fluid was alkaline with redox conditions above the hematite–magnetite buffer. We suggest that the precipitation mechanism for native elements, pitchblende and arsenides is a decrease in pH during fluid mixing processes. REE patterns in fluorite and the occurrence of Bi in all stages suggest a granitic source of some ore-forming elements, whereas, e.g. Ag, Co and Ni probably have been leached from the redbeds. The greater importance of Cu and isotope data indicates that the Miocene ore stage III is more influenced by fluids from the overlying redbeds and limestones than the earlier mineralization stages.  相似文献   

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Liu  Han-Lun  Han  Yi  Wang  Ke-Yong  Li  Wen  Li  Jian  Cai  Wen-Yan  Fu  Li-Juan 《Arabian Journal of Geosciences》2018,11(24):1-13
Arabian Journal of Geosciences - Soil toxic metal pollution is one of the most prominent environmental problems in the rapid industrialization of societies because of the considerable harm caused...  相似文献   

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The Tongshankou Cu–Mo deposit, located in the westernmost Daye district of the Late Mesozoic Metallogenic Belt along the Middle-Lower reaches of the Yangtze River, eastern China, consists mainly of porphyry and skarn ores hosted in the Tongshankou granodiorite and along the contact with the Lower Triassic marine carbonates, respectively. Sensitive high-resolution ion microprobe zircon U–Pb dating constrains the crystallization of the granodiorite at 140.6 ± 2.4 Ma (1σ). Six molybdenite samples from the porphyry ores yield Re–Os isochron age of 143.8 ± 2.6 Ma (2σ), while a phlogopite sample from the skarn ores yields an 40Ar/39Ar plateau age of 143.0 ± 0.3 Ma and an isochron age of 143.8 ± 0.8 Ma (2σ), indicating an earliest Cretaceous mineralization event. The Tongshankou granodiorite has geochemical features resembling slab-derived adakites, such as high Sr (740–1,300 ppm) and enrichment in light rare earth elements (REE), low Sc (<10 ppm), Y (<13.3 ppm), and depletion in heavy REE (<1.2 ppm Yb), and resultant high Sr/Y (60–92) and La/Yb (26–75) ratios. However, they differ from typical subduction-related adakites by high K, low MgO and Mg#, and radiogenic Sr–Nd–Hf isotopic compositions, with (87Sr/86Sr) t  = 0.7062–0.7067, ɛ Nd(t) = −4.37 to −4.63, (176Hf/177Hf) t  = 0.282469–0.282590, and ɛ Hf(t) = −3.3 to −7.6. The geochemical and isotopic data, coupled with geological analysis, indicate that the Tongshankou granodiorite was most likely generated by partial melting of enriched lithospheric mantle that was previously metasomitized by slab melts related to an ancient subduction system. Magmas derived from such a source could have acquired a high oxidation state, as indicated by the assemblage of quartz–magnetite–titanite–amphibole–Mg-rich biotite in the Tongshankou granodiorite and the compositions of magmatic biotite that fall in the field between the NiNiO and magnetite–hematite buffers in the Fe3+–Fe2+–Mg diagram. Sulfur would have been present as sulfates in such highly oxidized magmas, so that chalcophile elements Cu and Mo were retained as incompatible elements in the melt, contributing to subsequent mineralization. A compilation of existing data reveals that porphyry and porphyry-related Cu–Fe–Au–Mo mineralization from Daye and other districts of the Metallogenic Belt along the Middle-Lower reaches of the Yangtze River took place coevally in the Early Cretaceous and was related to an intracontinental extensional environment, distinctly different from the arc-compressive setting of the Cenozoic age that has been responsible for the emplacement of most porphyry Cu deposits of the Pacific Rim.  相似文献   

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Geology of Ore Deposits - The Koklan W–Mo deposit in Transuralia is confined to the eponymous Middle Permian leucogranitic pluton, which intrudes a sequence of the Lower Paleozoic crystalline...  相似文献   

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Milos Island contains several epithermal deposits (e.g., Profitis Ilias–Chondro Vouno Pb–Zn–Ag–Au–Te–Cu, Triades–Galana–Agathia–Kondaros Pb–Zn–Ag–Bi–W–Mo ± Cu–Au, and Katsimoutis–Kondaros–Vani Pb–Zn–Ag–Mn) of Late Pliocene to Early Pleistocene age. These deposits are hosted in calc-alkaline volcanic rocks emplaced as a result of three successive magma pulses in an emergent volcanic edifice: submarine rhyolitic to rhyodacitic cryptodomes at ca. 2.7. Ma (Profitis Ilias–Chondro Vouno), submarine to subaerial andesite to dacite domes at ca. 2.2 to 1.5 Ma (Triades–Galana–Kondaros–Katsimouti–Vani). Hydrothermal alteration of the volcanic rocks includes advanced argillic- (both hypogene and steam-heated), argillic, phyllic, adularia-sericite and propylitic types. In the northern sector (Triades–Galana–Agathia–Kondaros), initial magma degassing derived from andesitic–dacitic intrusives along NE–SW to E–W trending faults resulted in the development of pre-ore hypogene advanced argillic alteration (dickite, alunite, ± diaspore, pyrophyllite, halite, and pyrite) in a submarine environment. Mineralogical data indicate common features among the Profitis Ilias–Chondro Vouno, Kondaros–Katsimoutis–Vani and Triades–Galana mineralized centers, all of which are characterized by the presence of galena, Fe-poor sphalerite, and chalcopyrite as well as abundant barite, adularia, sericite and, to a lesser extent, calcite, which are typical of intermediate-sulfidation epithermal type deposits. Locally, at Triades–Galana and Kondaros–Agathia, high-sulfidation conditions prevailed as suggested by the presence of coexisting enargite and covellite. The high silver and gold content of the western Milos deposits is derived from Ag-bearing sulfosalts (polybasite, pearceite, pyrargyrite, freibergite) and tellurides. Gold at Profitis Ilias, both as native gold and silver-gold tellurides, is present in base-metal precipitates within multicomponent blebs, which recrystallized to form hessite, petzite, altaite, coloradoite, and native gold. Mineralogical evidence (e.g. microchimney structures, copper sulfides, widespread occurrence of barite, aragonite) suggests that precious metal mineralization in western Milos mineralization formed in a submarine setting.We present information on the surface distribution of Au, Ag, Cu, Pb, Zn, As, Sb, Hg, Mo, Bi, W and Cd at western Milos. Gold is enriched at Profitis Ilias–Chondro Vouno deposits and to a lesser extent at Triades–Galana. Arsenic is absent from the southern sector but shows elevated concentrations together with molybdenum, bismuth and tungsten at the northern sector (Triades–Galana, Vani deposits). The differences in precious and base metal abundances may be related to the depths at which the deposits are exposed, and/or different sources of magma. The metal signatures of the Triades–Galana and Agathia–Kondaros–Katsimouti–Vani (Mo–Bi–W–As–Hg–Ag–Au) occurrences compared to Profitis Ilias (Te–Au–Ag) reflect different sources of magma (dacite–rhyodacite for Profitis Ilias, andesite–dacite for Triades–Galana, and dacite for Kondaros–Katsimoutis). The enrichment of Te, Mo, W, and Bi in the deposits is a strong indication of a direct magmatic contribution of these metals.At western Milos, precious and base-metal vein mineralization was deposited during episodic injection of magmatic volatiles and dilution of the hydrothermal fluids by seawater. The mineralization represents seafloor/sub-seafloor precipitation of sulfides that formed in stockwork zones. Base and precious metal mineralization formed from intermediate- to high-sulfidation state fluids and mostly under boiling conditions as indicated by the widespread occurrence of adularia associated with metallic mineralization. We speculate that the widespread occurrence of boiling and the shallow depth of the precious- and base-metal emplacement prevented the formation of seafloor massive sulfides.  相似文献   

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《International Geology Review》2012,54(15):1835-1864
The Yinshan deposit is a large epithermal-porphyry polymetallic deposit, and the timing and petrogenesis of ore-hosting porphyries have been hotly debated. We present new results from geochemical, whole-rock Sr–Nd and zircon U–Pb–Hf–O isotopic investigations. Zircon U–Pb data demonstrate that the quartz porphyry, dacitic porphyry, and quartz dioritic porphyry formed at ?172.2 ± 0.4 Ma, ?171.7 ± 0.5 Ma, and ?170.9 ± 0.3 Ma, respectively. Inherited zircon cores show significant age spreads from ?730 to ?1390 Ma. Geochemically, they are high-K calc-alkaline or shoshonitic rocks with arc-like trace element patterns. They have similar whole-rock Nd and zircon Hf isotopic compositions, yet an increasing trend in ?Nd(t) and ?Hf(t) values typifies the suite. Older (inherited) zircons of the three porphyries display Hf compositions comparable to those of the Jiangnan Orogen basement rocks. In situ zircon oxygen isotopic analyses reveal that they have similar oxygen isotopic compositions, which are close to those of mantle zircons. Moreover, a decreasing trend of δ18O values is present. We propose that the ore-related porphyries of the Yinshan deposit were emplaced contemporaneously and derived from partial melting of Neoproterozoic arc-derived mafic (or ultra-mafic) rocks. Modelling suggests that the quartz porphyries, dacitic porphyries, and quartz dioritic porphyries experienced ?25%, ?10%, and ?10% crustal contaminations by Shuangqiaoshan rocks. Our study provides important constraints on mantle–crust interaction in the genesis of polymetallic mineralization associated with Mesozoic magmatism in southeastern China.  相似文献   

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The Yindongpo gold deposit is located in the Weishancheng Au–Ag-dominated polymetallic ore belt in Tongbai Mountains, central China. The ore bodies are stratabound within carbonaceous quartz–sericite schists of the Neoproterozoic Waitoushan Group. The ore-forming process can be divided into three stages, represented by early barren quartz veins, middle polymetallic sulfide veinlets and late quartz–carbonate stockworks, with most ore minerals, such as pyrite, galena, native gold and electrum being formed in the middle stage. The average δ18Owater values changed from 9.7‰ in the early stage, through 4.9‰ in the middle stage, to − 5.9‰ in the late stage, with the δD values ranging between − 65‰ and − 84‰. The δ13CCO2 values of ore fluids are between − 3.7‰ and + 6.7‰, with an average of 1.1‰. The H–O–C isotope systematics indicate that the ore fluids forming the Yindongpo gold deposit were probably initially sourced from a process of metamorphic devolatilization, and with time gradually mixed with meteoric water. The δ34S values range from − 0.3‰ to + 5.2‰, with peaks ranging from + 1‰ to + 4‰. Fourteen sulfide samples yield 206Pb/204Pb values of 16.990–17.216, 207Pb/204Pb of 15.419–15.612 and208Pb/204Pb of 38.251–38.861. Both S and Pb isotope ratios are similar to those of the main lithologies of the Waitoushan Group, but differ from other lithologic units and granitic batholiths in the Tongbai area, which suggest that the ore metals and fluids originated from the Waitoushan Group. The available K–Ar and 40Ar/39Ar ages indicate that the ore-forming process mainly took place in the period of 176–140 Ma, during the transition from collisional compression to extension and after the closure of the oceanic seaway in the Qinling Orogen. The Yindongpo gold deposit is interpreted as a stratabound orogenic-style gold system formed during the transition phase from collisional compression to extension.The ore metals in the Waitoushan Group were extracted, transported and then accumulated in the carbonaceous sericite schist layer. The carbonaceous sericite schist layer, especially at the junction of collapsed anticline axis and fault structures, became the most favorable locus for the ore bodies.  相似文献   

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The Huangshaping polymetallic deposit is located in southeastern Hunan Province, China. It is a world-class W–Mo–Pb–Zn–Cu skarn deposit in the Nanling Range Metallogenic Belt, with estimated reserves of 74.31 Mt of W–Mo ore at 0.28% WO3 and 0.07% Mo, 22.43 Mt of Pb–Zn ore at 3.6% Pb and 8.00% Zn, and 20.35 Mt of Cu ore at 1.12% Cu. The ore district is predominantly underlained by carbonate formations of the Lower Carboniferous period, with stocks of quartz porphyry, granite porphyry, and granophyre. Skarns occurred in contact zones between stocks and their carbonate wall rocks, which are spatially associated with the above-mentioned three types of ores (i.e., W–Mo, Pb–Zn, and Cu ores).Three types of fluid inclusions have been identified in the ores of the Huangshaping deposit: aqueous liquid–vapor inclusions (Type I), daughter-mineral-bearing aqueous inclusions (Type II), and H2O–CO2 inclusions (Type III). Systematic microthermometrical, laser Raman spectroscopic, and salinity analyses indicate that high-temperature and high-salinity immiscible magmatic fluid is responsible for the W–Mo mineralization, whereas low-temperature and low-salinity magmatic-meteoric mixed fluid is responsible for the subsequent Pb–Zn mineralization. Another magmatic fluid derived from deep-rooted magma is responsible for Cu mineralization.Chondrite-normalized rare earth element patterns and trace element features of calcites from W–Mo, Pb–Zn, and Cu ores are different from one another. Calcite from Cu ores is rich in heavy rare earth elements (187.4–190.5 ppm), Na (0.17%–0.19%), Bi (1.96–64.60 ppm), Y (113–135 ppm), and As (9.1–29.7 ppm), whereas calcite from W–Mo and Pb–Zn ores is rich in Mn (> 10.000 ppm) and Sr (178–248 ppm) with higher Sr/Y ratios (53.94–72.94). δ18O values also differ between W–Mo/Pb–Zn ores (δ18O = 8.10‰–8.41‰) and Cu ores (δ18O = 4.34‰–4.96‰), indicating that two sources of fluids were, respectively, involved in the W–Mo, Pb–Zn, and Cu mineralization.Sulfur isotopes from sulfides also reveal that the large variation (4‰–19‰) within the Huangshaping deposit is likely due to a magmatic sulfur source with a contribution of reduced sulfate sulfur host in the Carboniferous limestone/dolomite and more magmatic sulfur involved in the Cu mineralization than that in W–Mo and Pb–Zn mineralization. The lead isotopic data for sulfide (galena: 206Pb/204Pb = 18.48–19.19, 207/204Pb = 15.45–15.91, 208/204Pb = 38.95–39.78; sphalerite: 206Pb/204Pb = 18.54–19.03, 207/204Pb = 15.60–16.28, 208/204Pb = 38.62–40.27; molybdenite: 206Pb/204Pb = 18.45–19.21, 207/204Pb = 15.53–15.95, 208/204Pb = 38.77–39.58 chalcopyrite: 206Pb/204Pb = 18.67–19.38, 207/204Pb = 15.76–19.90, and 208/204Pb = 39.13–39.56) and oxide (scheelite: 206Pb/204Pb = 18.57–19.46, 207/204Pb = 15.71–15.77, 208/204Pb = 38.95–39.13) are different from those of the wall rock limestone (206Pb/204Pb = 18.34–18.60, 207/204Pb = 15.49–15.69, 208/204Pb = 38.57–38.88) and porphyries (206Pb/204Pb = 17.88–18.66, 207/204Pb = 15.59–15.69, 208/204Pb = 38.22–38.83), suggesting Pb206-, U238-, and Th 232-rich material are involved in the mineralization. The Sm–Nd isotopes of scheelite (εNd(t) =  6.1 to − 2.9), garnet (εNd(t) =  6.8 to − 6.1), and calcite (εNd(t) =  6.3) from W–Mo ores as well as calcite (εNd(t) =  5.4 to − 5.3) and scheelite (εNd(t) =  2.9) from the Cu ores demonstrate suggest more mantle-derived materials involved in the Cu mineralization.In the present study we conclude that two sources of ore-forming fluids were involved in production of the Huangshaping W–Mo–Pb–Zn–Cu deposit. One is associated with the granite porphyry magmas responsible for the W–Mo and then Pb–Zn mineralization during which its fluid evolved from magmatic immiscible to a magmatic–meteoritic mixing, and the other is derived from deep-rooted magma, which is related to Cu-related mineralization.  相似文献   

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Geology of Ore Deposits - Abstract—The paper presents the results of mineralogical studies of tin–silver–polymetallic ores localized at the deep level (500–700 m below the...  相似文献   

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Acta Geochimica - Three monogenetic cones in the Baossi–Warack area, Ngaoundéré, Adamawa Plateau forming part of the Cameroon Volcanic Line (CVL) are documented in this study....  相似文献   

18.
《International Geology Review》2012,54(14):1786-1800
Geochronology, geochemistry, and whole-rock Sr–Nd–Pb isotopes were studied on a suite of Mesozoic adamellites from eastern China to characterize their ages and petrogenesis. Sensitive high-resolution ion microprobe U–Pb zircon analyses were done, yielding consistent ages of 123.2 ± 1.8 to 122.1 ± 2.1 Ma for the samples. These rocks belong to the alkaline magma series in terms of K2O + Na2O contents (8.45–9.58 wt.%) and to the shoshonitic series based on their high K2O contents (5.23–5.79 wt.%). The adamellites are further characterized by high light rare earth element contents [(La/Yb)N = 14.96–45.99]; negative Eu anomalies (δEu = 0.46–0.75); positive anomalies in Rb, Th, Pb, and U; and negative anomalies in Sr, Ba, and high field-strength elements (i.e. Nb, Ta, P, and Ti). In addition, all of the adamellites in this study display relatively low radiogenic Sr [(87Sr/86Sr)i = 0.7081–0.7089] and negative ?Nd(t) values from –16.70 to –17.80. These results suggest that the adamellites were derived from low-degree partial melting of an enriched lithospheric mantle below the North China Craton (NCC). The parent magmas likely experienced fractional crystallization of potassium feldspar, plagioclase and Fe–Ti oxides (e.g. rutile, ilmenite, and titanite), apatite, and zircon during the ascent of alkaline rocks without crustal contamination.  相似文献   

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International Journal of Earth Sciences - In the present study we investigate the microstructural development in mullite, quartz and garnet in an anatectic migmatite hosted within a Grenvillian-age...  相似文献   

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The Pb–Zn–Ag quartz vein from Terramonte cuts the Neoproterozoic–Cambrian schist–greywacke complex. This orebody was partially exploited. The paragenetic sequence consists of four stages containing quartz accompanied mainly by arsenopyrite and pyrite in the first stage, sphalerite in the second stage, galena showing many inclusions of several sulphosalts in the third stage and carbonates in the fourth remobilization stage. Several sulphide and sulphosalt grains are oscillatory zoned. The chemical distinction between lighter and darker zones in backscattered images of arsenopyrite, pyrite, sphalerite and freibergite is due to substitutions in the mineral lattices. But the distinction between these zones in semseyite is due to a higher Pb content and a lower Sb content in the lighter zone than in the darker zone and the metal and metalloid are the main constituents in the solid solution, but are not correlated. The Sb, Ag and Bi substitute for Pb in galena, but did not cause any zoning. Ore deposition was possible due to mixing of a hypersaline fluid with up to 26 wt.% NaCl equivalent (and occasionally with CaCl2 up to 17 wt.%), which carried the metallic content of the fluid, with an extremely low salinity fluid of presumed meteoric origin that percolated down into the basement. The metals could have been leached from a mixture of mainly metasediments and also previous Sb–Au deposits by fluids that acquire high salinity in one of two probable ways: leaching of salt beds or following seawater evaporation. The entire mineralizing event probably occurred at a relatively low temperature, possibly between 120 and 230 °C. Remobilization of Pb, Zn, Ag, As, Sb and Cu will be due to the tectonic evolution of the opening of the Atlantic Ocean. This vein is probably of Alpine age.  相似文献   

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