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1.
The Yinchanggou Pb-Zn deposit, located in southwestern Sichuan Province, western Yangtze Block, is stratigraphically controlled by late Ediacaran Dengying Formation and contains >0.3 Mt of metal reserves with 11 wt% Pb + Zn. A principal feature is that this deposit is structurally controlled by normal faults, whereas other typical deposits nearby (e.g. Maozu) are controlled by reverse faults. The origin of the Yinchanggou deposit is still controversial. Ore genetic models, based on conventional whole-rock isotope tracers, favor either sedimentary basin brine, magmatic water or metamorphic fluid sources. Here we use in situ Pb and bulk Sr isotope features of sulfide minerals to constrain the origin and evolution of hydrothermal fluids. The Pb isotope compositions of galena determined by femtosecond LA-MC-ICPMS are as follows: 206Pb/204Pb = 18.17–18.24, 207Pb/204Pb = 15.69–15.71, 208Pb/204Pb = 38.51–38.63. These in situ Pb isotope data overlap with bulk-chemistry Pb isotope compositions of sulfide minerals (206Pb/204Pb = 18.11–18.40, 207Pb/204Pb = 15.66–15.76, 208Pb/204Pb = 38.25–38.88), and both sets of data plotting above the Pb evolution curve of average upper continental crust. Such Pb isotope signatures suggest an upper crustal source of Pb. In addition, the coarse-grained galena in massive ore collected from the deep part has higher 206Pb/204Pb ratios (18.18–18.24) than the fine-grained galena in stockwork ore sampled from the shallow part (206Pb/204Pb = 18.17–18.19), whereas the latter has higher 208Pb/204Pb ratios (38.59–38.63) than the former (208Pb/204Pb = 38.51–38.59). However, both types of galena have the same 207Pb/204Pb ratios (15.69–15.71). This implies two independent Pb sources, and the metal Pb derived from the basement metamorphic rocks was dominant during the early phase of ore formation in the deep part, whereas the ore-hosting sedimentary rocks supplied the majority of metal Pb at the late phase in the shallow part. In addition, sphalerite separated from different levels has initial 87Sr/86Sr ratios ranging from 0.7101 to 0.7130, which are higher than the ore formation age-corrected 87Sr/86Sr ratios of country sedimentary rocks (87Sr/86Sr200 Ma = 0.7083–0.7096), but are significantly lower than those of the ore formation age-corrected basement rocks (87Sr/86Sr200 Ma = 0.7243–0.7288). Again, such Sr isotope signatures suggest that the above two Pb sources were involved in ore formation. Hence, the gradually mixing process of mineralizing elements and associated fluids plays a key role in the precipitation of sulfide minerals at the Yinchanggou ore district. Integrating all the evidence, we interpret the Yinchanggou deposit as a strata-bound, normal fault-controlled epigenetic deposit that formed during the late Indosinian. We also propose that the massive ore is formed earlier than the stockwork ore, and the temporal-spatial variations of Pb and Sr isotopes suggest a certain potential of ore prospecting in the deep mining area.  相似文献   

2.
The Wangjiazhuang porphyry–breccia Cu(–Mo) deposit is located in the Zouping volcanic basin, western Shandong Province. Seven molybdenite samples yield a Re–Os weighted mean age of 127.8 ± 0.7 Ma (2σ), which is identical within error to the zircon weighted mean 206Pb/238U age of 128.3 ± 1.3 Ma (2σ) determined for quartz monzonite samples. The host rock is characterized by high concentrations of K2O (4.26–4.53 wt.%), Na2O (4.97–5.76 wt.%), LILEs and LREEs, and high Mg# (> 40), and low concentrations of HFSEs and HREEs, with K2O/Na2O ratios of 0.76–0.88. The quartz monzonite also has high Sr/Y (69.9–112.5) and (La/Yb)N (22.0–30.0) ratios, similar to adakitic rocks worldwide. Relatively low initial 87Sr/86Sr ratios (0.70549–0.70556), high εNd(t) values (2.58–3.06), high radiogenic Pb [(206Pb/204Pb)i = 18.3424–18.4606, (207Pb/204Pb)i = 15.5692–15.5985, (208Pb/204Pb)i = 38.1714–38.2734] and high zircon εHf(t) values (− 2.1 to + 4.3) indicate that the magma was likely derived from the partial melting of subducted oceanic crust which then reacted with the peridotitic mantle wedge. Both the breccia and porphyry ores have a narrow range of δ34S (− 4.8 to + 2.1‰) and Pb isotopic compositions (206Pb/204Pb = 18.295–18.402, 207Pb/204Pb = 15.551–15.573, and 208Pb/204Pb = 38.215–38.331), suggesting that the ore metals were extracted primarily from the quartz monzonite or similar source. Subduction of the Paleo-Pacific slab during the Early Cretaceous resulted in the formation of the Wangjiazhuang quartz monzonite and associated Cu(–Mo) deposit in western Shandong Province.  相似文献   

3.
Major, trace element and isotopic (Sr, Nd, Pb) data and unspiked K–Ar ages are presented for Quaternary (0.90–0.95 Ma old) basalts from the Hayyabley volcano, Djibouti. These basalts are LREE-depleted (Lan/Smn = 0.76–0.83), with 87Sr/86Sr ratios ranging from 0.70369 to 0.70376, and rather homogeneous 143Nd/144Nd (εNd = + 5.9–+ 7.3) and Pb isotopic compositions (206Pb/204Pb = 18.47–18.55, 207Pb/204Pb = 15.52–15.57, 208Pb/204Pb = 38.62–38.77). They are very different from the underlying enriched Tadjoura Gulf basalts, and from the N-MORB erupted from the nascent oceanic ridges of the Red Sea and Gulf of Aden. Their compositions closely resemble those of (1) depleted Quaternary Manda Hararo basalts from the Afar depression in Ethiopia and (2) one Oligocene basalt from the Ethiopian Plateau trap series. Their trace element and Sr, Nd, Pb isotope systematics suggest the involvement of a discrete but minor LREE-depleted component, which is probably an intrinsic part of the Afar plume.  相似文献   

4.
The Huangshaping granites in Hunan Province, South China were investigated for their geochemical characteristics. Three types of granites have been petrographically identified: quartz porphyry, granophyre, and granite porphyry. Whole rock geochemistry suggests that the Huangshaping granites, especially the granite porphyry, exhibit typical A-type granite characteristics with their enrichment in Si, Rb, U, Th, and Nb and significant depletion in Ba, Sr, Ti, Eu, and P. Based on the Al, Y and Zr contents as well as the REE patterns of the rocks investigated, the quartz porphyry and the granophyre are classified as A1 type alkaline granites whereas the granite porphyry is considered as A2 type aluminous granite. Whole rock and quartz/feldspar O isotope data yields a wide range of δ18OSMOW values (11.09–26.32‰). The granites are characterized by high radiogenic Pb isotopic composition. The present-day whole rock Pb isotopic ratios are 206Pb/204Pb = 18.706–19.155, 207Pb/204Pb = 15.616–15.711 and 208Pb/204Pb = 38.734–39.296. Combining the O–Pb isotope compositions with major, trace and REE geochemistry and regional geology characteristics, the Huangshaping granites were determined to resemble within-plate granites that were mainly derived from a felsic infracrustal source related to continental extension. The magma source of the quartz porphyry and the granophyre may have been generated from deeper depths, and then ascended rapidly with limited water content and low oxygen fugacity, which contributed to Cu, Pb and Zn mineralization. On the other hand, the magma that generated the granite porphyry may have ascended relatively slower and experienced pronounced crystal fractionation, upper-crustal basement rock contamination (assimilation) and wall–rock interaction, producing the Sn- and W-rich granite porphyry. This study reveals the crustal extension process and associated magmatic–metallogenic activities during 180–150 Ma in South Hunan.  相似文献   

5.
The Nanling Range in South China is characterized by extensive Mesozoic magmatism and coeval nonferrous and rare metal mineralization. Huangshaping is a world-class Pb-Zn-W-Mo polymetallic skarn deposit in the central Nanling Range. Magmatic rocks occurring in this ore district include quartz porphyry, granite porphyry, granophyre, dacite porphyry, and aplite, with only the first three granitoids genetically associated with polymetallic mineralization. Most of the orebodies are constrained within the contact zones as skarn and veins between these granitic stocks and the carbonate wall rocks.Since the age of the quartz porphyry is still controversial, and studies of the dacite porphyry and aplite are absent, we focus on these magmatic rocks first. LA-ICP-MS zircon U-Pb dating suggests that the crystallization ages of the quartz porphyry, dacite porphyry, and aplite are 154.3 ± 1.9 Ma, 158.1 ± 0.8 Ma, and 148.4 ± 3.4 Ma, respectively. Combined with previously published age data, we infer the evolutionary sequence of magmatic rocks should be dacite porphyry → quartz porphyry → granite porphyry (granophyre) → aplite. The quartz porphyry, dacite porphyry, and aplite yield high contents of high field strength elements (Zr + Nb + Ce + Y = 255–440 ppm), high ratios of 10,000 × Ga/Al (2.6–3.2), and prominent depletions in Ba, Sr, Eu, P, and Ti, indicating their crustal affinities to A-type granites. They have negative εNd(t) values (−9.4 to −7.0) and high initial Pb isotopic ratios (206Pb/204Pbi = 18.307–18.644, 207Pb/204Pbi = 15.689–15.742, 208Pb/204Pbi = 38.589–38.986), suggesting that they were probably derived by partial melting of ancient granulitic crustal materials.The sulfide minerals exhibit a wide range of δ34SV-CDT values from −22.6 to 24.2‰, with 206Pb/204Pb of 17.669–19.708, 207Pb/204Pb of 15.492–15.714, and 208Pb/204Pb of 37.880–39.789, indicating that sulfur, lead, and other associated metals were derived from a mixture of magmatic components and the Carboniferous wall rocks. Fluid inclusions in pyrrhotite, sphalerite, and marmatite samples have 3He/4He ratios of 0.12 to 1.53 Ra, with calculated mantle helium proportions of 1.3 to 18.9%, indicating a predominantly crustal origin for the ore fluids, with minor inputs from the mantle. The Huangshaping deposit is a typical example of the genetic relationship both spatially and temporally between Jurassic magmatism and polymetallic metallogeny in the Nanling Range.  相似文献   

6.
The southern Great Xing'an Range is one of the most important metallogenic belts in northern China, and contains numerous Pb–Zn–Ag–Cu–Sn–Fe–Mo deposits. The Huanggang iron–tin polymetallic skarn deposit is located in the Sn-polymetallic metallogenic sub-belt. Skarns and iron orebodies occur as lenses along the contact between granite plutons and the Lower Permian Huanggangliang Formation marble or Dashizhai Formation andesite. Field evidence and petrographic observations indicate that the three stages of hydrothermal activity, i.e., skarn, oxide and sulfide stages, all contributed to the formation of the Huanggang deposit.The skarn stage is characterized by the formation of garnet and pyroxene, and high-temperature, hypersaline hydrothermal fluids with isotopic compositions that are similar to those of typical magmatic fluids. These fluids most likely were generated by the separation of brine from a silicate melt instead of being a product of aqueous fluid immiscibility. The iron oxide stage coincides with the replacement of garnet and pyroxene by amphibole, chlorite, quartz and magnetite. The hydrothermal fluids of this stage are represented by L-type fluid inclusions that coexist with V-type inclusions with anomalously low δD values (approximately − 100 to − 116‰). The decrease in ore fluid δ18OH2O values with time coincides with marked decreases in the fluid salinity and temperature. Based on the fluid inclusion and stable isotopic data, the ore fluid evolved by boiling of the magmatic brine. The sulfide stage is characterized by the development of sphalerite, chalcopyrite, fluorite, and calcite veins, and these veins cut across the skarns and orebodies. The fluids during this stage are represented by inclusions with a variable but continuous sequence of salinities, mainly low-salinity inclusions. These fluids yield the lowest δ18OH2O values and moderate δD values ( − 1.6 to − 2.8‰ and − 101 to − 104‰, respectively). The data indicate that the sulfide stage fluids originated from the mixing of residual oxide-stage fluids with various amounts of meteoric water. Boiling occurred during this stage at low temperatures.The sulfur isotope (δ34S) values of the sulfides are in a narrow range of − 6.70 to 4.50‰ (mean = − 1.01‰), and the oxygen isotope (δ18O) values of the magnetite are in a narrow range of 0.1 to 3.4‰. Both of these sets of values suggest that the ore-forming fluid is of magmatic origin. The lead isotope compositions of the ore (206Pb/204Pb = 18.252–18.345, 207Pb/204Pb = 15.511–15.607, and 208Pb/204Pb = 38.071–38.388) are consistent with those of K-feldspar granites (206Pb/204Pb = 18.183–18.495, 207Pb/204Pb = 15.448–15.602, 208Pb/204Pb = 37.877–38.325), but significantly differ from those of Permian marble (206Pb/204Pb = 18.367–18.449, 207Pb/204Pb = 15.676–15.695, 208Pb/204Pb = 38.469–38.465), which also suggests that the ore-forming fluid is of magmatic origin.  相似文献   

7.
The recently discovered Guanfang large W deposit, in Yunnan Province, southwest China, is located in the Diandongnan thrust-nappe fold belt in the western part of the Cathaysia Block. The orebodies occur at the contacts between the Suozuodi granite and Middle Cambrian marbles. LA-ICP-MS zircon UPb dating of the ore-bearing Suozuodi granite yields a crystallization age of 91.6 ± 1.0 Ma (MSWD = 0.56). An isochron age of 91.6 ± 1.3 Ma (MSWD = 0.24) was obtained by ReOs dationg of five molybdenite samples separated from sulfide-bearing ores. Scheelite at the Guanfang deposit is characterized by broad rangs of Pb isotopic ratios (207Pb/204Pb = 15.568 to 15.735, 206Pb/204Pb = 17.912 to 18.390, 208Pb/204Pb = 38.491 to 38.730) and high initial 87 Sr/86 Sr ratios (Isr = 0.7118 to 0.7140), which consistent with the isotopic characteristics of the Suozuodi granite. Pb and Sr isotopic results indicate that the ore-forming materials were derived from a crustal source, without addition of mantle materials. The Guanfang tungsten deposit was formed in a syn-collision tectonic setting during the late stage of the Yanshanian tectonism.  相似文献   

8.
The Hongshan Cu-polymetallic deposit is located in the southern Yidun arc in southwestern China, where both subduction-related (Late Triassic) and post-collisional (Late Cretaceous) porphyry–skarn–epithermal mineralization systems have been previously recognized. In this study, two distinct magmatic events, represented by diorite porphyry and quartz monzonite porphyry, have been revealed in the Hongshan deposit, with zircon SHRIMP U–Pb ages of 214 ± 2 Ma and 73.4 ± 0.7 Ma, respectively. The 73 Ma age is comparable to the Re–Os ages of 77 to 80 Ma of ore minerals from the Hongshan deposit, indicating that the mineralization is related to the Late Cretaceous quartz monzonite porphyries rather than Late Triassic diorite porphyries. The Late Triassic diorite porphyries belong to the high-K calc-alkaline series and show arc magmatic geochemical characteristics such as enrichment in Rb, Ba, Th and U and depletion in HFSEs, indicating that they were formed during the westward subduction of the Garzê–Litang Ocean. In contrast, the Late Cretaceous quartz monzonite porphyries show shoshonitic I-type geochemical characteristics, with high SiO2, K2O, LILE, low HREE, Y and Yb contents, and high LREE/HREE and La/Yb ratios. These geochemical characteristics, together with the Sr–Nd–Pb isotopic compositions (average (87Sr/86Sr)i = 0.7085; εNd(t) = − 6.0; 206Pb/204Pb = 19.064, 207Pb/204Pb = 15.738, 208Pb/204Pb = 39.733) suggest that the quartz monzonite porphyries originated from the partial melting of the ancient lower crust in response to underplating of mafic magma from subduction metasomatized mantle lithosphere, possibly triggered by regional extension in the post-collisional tectonic stage. The S isotopic compositions (δ34SV-CDT = 3.81‰ to 5.80‰) and Pb isotopic compositions (206Pb/204Pb = 18.014 to 18.809, 207Pb/204Pb = 15.550 to 15.785, and 208Pb/204Pb = 38.057 to 39.468) of ore sulfides indicate that the sulfur and metals were derived from mixed mantle and crustal sources. It is proposed that although the Late Triassic magmatic event is not directly related to mineralization, it contributed to the Late Cretaceous mineralization system through the storage of large amounts of sulfur and metals as well as water in the cumulate zone in the mantle lithosphere through subduction metasomatism. Re-melting of the mantle lithosphere including the hydrous cumulate zone and ancient lower crust during the post-collisional stage produced fertile magmas, which ascended to shallow depths to form quartz monzonite porphyries. Hydrothermal fluids released from the intrusions resulted in porphyry-type Mo–Cu ores in and near the intrusions, skarn-type Cu–Mo ores in the country rocks above the intrusions, and hydrothermal Pb–Zn ores in the periphery.  相似文献   

9.
The Zhifang Mo deposit is located in the northeastern Qinling Orogen along the southern margin of the North China Craton. The deposit represents a quartz-vein system hosted in the Mesoproterozoic Xiong'er Group volcanic rocks. We identify three hydrothermal stages (early, middle and late), characterized by veinlets of quartz–pyrite, quartz–molybdenite–pyrite–chalcopyrite–galena–sphalerite, and quartz–carbonate assemblages, respectively. Five molybdenite samples from the Zhifang deposit yield Re–Os ages ranging from 241.2 ± 1.6 Ma to 247.4 ± 2.5 Ma, with an isochron age of 246.0 ± 5.2 Ma (2σ, MSWD = 7.4), and a weighted mean age of 243.8 ± 2.8 Ma (2σ, MSWD = 5.5). The Re–Os age shows that the Mo mineralization occurred during the Indosinian Orogeny, and suggests that the mineralization is unrelated to the Yanshanian magmatism or the Paleo-Mesoproterozoic volcanic–hydrothermal event.This study also reports a new Sr–Nd–Pb isotope dataset from ore sulfides in an attempt to constrain the source of the ore-forming fluids. Ten sulfide samples from middle stage of the Zhifang Mo deposit yield ISr(t) ratios of 0.710286–0.711943, with an average of 0.711004; εNd(t) values between − 19.5 and − 14.8, with an average of − 16.7; and (206Pb/204Pb)i, (207Pb/204Pb)i and (208Pb/204Pb)i ratios of 17.126–17.535, 15.374–15.466 and 37.485–37.848, with averages of 17.380, 15.410 and 37.631, respectively. One pyrite from the early stage yield ISr(t) of 0.722711–0.722855, with an average of 0.722783, which is higher than those of the middle stage sulfides and suggests equilibration with wallrocks. The εNd(t) values are in the range of − 17.3 to − 16.6 with a mean at − 17.0; and (206Pb/204Pb)i, (207Pb/204Pb)i and (208Pb/204Pb)i ratios are 17.386, 15.405 and 37.622, respectively. The ore sulfides show higher Pb-isotope ratios, higher εNd(t) and lower ISr(t) values than the host rocks. The results suggest that the ore-forming fluids had lower ISr(t), and higher εNd(t) values than the ore sulfides, and were possibly sourced from the Dengfeng Complex. The southward subduction of the North China Craton beneath the Huaxiong Block during the Triassic was possibly responsible for the formation of the Waifangshan orogenic Mo system.  相似文献   

10.
The Wunugetushan porphyry Cu–Mo deposit is located in the Manzhouli district of NE China, on the southern margin of the Mesozoic Mongol–Okhotsk Orogenic Belt. Concentric rings of hydrothermal alteration and Cu–Mo mineralization surround an Early–Middle Jurassic monzogranitic porphyry. The Cu–Mo mineralization is clearly related to the quartz–potassic and quartz–sericite alteration. Molybdenite Re–Os and groundmass 40Ar/39Ar of the host porphyry dates indicate that the ore-formation and porphyry-emplacement occurred at 177.6 ± 4.5 Ma and 179.0 ± 1.9 Ma, respectively. Geochemically, the host porphyry of the deposit is characterized by strong LREE/HREE fractionation, enrichment in LILE, Ba, Rb, U, Th and Pb, and depletion of HFSE, Nb, Ta, Ti and HREE. The Sr–Nd–Pb isotopic compositions of the porphyry display an varied initial (87Sr/86Sr)i ratio, a positive εNd(t) values and high 206Pb/204Pbt, 207Pb/204Pbt and 208Pb/204Pbt ratios. These data indicate that the magmatic source of the host porphyry comprised two end-members: lithospheric mantle metasomatized by fluids derived from the subducted slab; and continental crust. We infer that the primitive magma of the host porphyry was derived from crust–mantle transition zone. Based on regional geology and geochemistry of the host porphyry, the Wunugetushan deposit is suggested to form in a continental collision environment after closure of the Mongol–Okhotsk Ocean.  相似文献   

11.
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   

12.
Lead concentrations and stable lead isotopes (204Pb, 206Pb, 207Pb, 208Pb) were measured in forest moss samples (Pleurozium schreberi or Scleropodium purum) collected at 273 sites across the Czech Republic during 2010. Continuously decreasing median Pb concentrations in moss were documented over the last two decades: 1995: 11 mg/kg, 2000: 5.66 mg/kg, 2005: 4.94 mg/kg and 2010: 2.85 mg/kg. Several local anomalies have decreased in scale, the overall regional distribution patterns remained, however, the same. The regional Pb isotope ratio distributions show that the ratios show little variation for a large central part of the country and provide the large-scale background isotope ratios for the Czech Republic of about 204Pb/206Pb = 0.0550, 206Pb/207Pb = 1.167, 206Pb/208Pb = 0.478 and 207Pb/208Pb = 0.409 for 2010. This background Pb isotope ratio signal in moss has been locally (900–7500 km2) modified by specific Pb isotopic ratio signals caused by deposition of Pb emissions from known local anthropogenic Pb emission sources, such as industrial combustion of local coal, and a variety of industrial enterprises (metallurgical, engineering and glass works). At some sites where mining of uranium and polymetallic ores took place the moss samples show also a locally specific Pb isotope signal. The in terms of area affected largest deviations in the Pb-isotope ratios, e.g., in the Bohemian Massif, may be due to the input of geogenic dust.  相似文献   

13.
The Tianqiao Pb–Zn deposit in the western Yangtze Block, southwest China, is part of the Sichuan–Yunnan–Guizhou (SYG) Pb–Zn metallogenic province. Ore bodies are hosted in Devonian and Carboniferous carbonate rocks, structurally controlled by a thrust fault and anticline, and carried about 0.38 million tons Pb and Zn metals grading > 15% Pb + Zn. Both massive and disseminated Pb–Zn ores occur either as veinlets or disseminations in dolomitic rocks. They are composed of ore minerals, pyrite, sphalerite and galena, and gangue minerals, calcite and dolomite. δ34S values of sulfide minerals range from + 8.4 to + 14.4‰ and display a decreasing trend from pyrite, sphalerite to galena (δ34Spyrite > δ34Ssphalerite > δ34Sgalena). We interpret that reduced sulfur derived from sedimentary sulfate (gypsum and barite) of the host Devonian to Carboniferous carbonate rocks by thermal–chemical sulfate reduction (TSR). δ13CPDB and δ18OSMOW values of hydrothermal calcite range from –5.3 to –3.4‰ and + 14.9 to + 19.6‰, respectively, and fall in the field between mantle and marine carbonate rocks. They display a negative correlation, suggesting that CO2 in the hydrothermal fluid was a mixture origin of mantle, marine carbonate rocks and sedimentary organic matter. Sulfide minerals have homogeneous and low radiogenic Pb isotope compositions (206Pb/204Pb = 18.378 to 18.601, 207Pb/204Pb = 15.519 to 15.811 and 208Pb/204Pb = 38.666 to 39.571) that are plotted in the upper crust Pb evolution curve and overlap with that of Devonian to Carboniferous carbonate rocks and Proterozoic basement rocks in the SYG province. Pb isotope compositions suggest derivation of Pb metal from mixed sources. Sulfide minerals have 87Sr/86Sr ratios ranging from 0.7125 to 0.7167, higher than Sinian to Permian sedimentary rocks and Permian Emeishan flood basalts, but lower than basement rocks. Again, Sr isotope compositions are supportive of a mixture origin of Sr. They have an Rb–Sr isotopic age of 191.9 ± 6.9Ma, possibly reflecting the timing of Pb–Zn mineralization. C–O–S–Pb–Sr isotope compositions of the Tianqiao Pb–Zn deposit indicate a mixed origin of ore-forming fluids, which have Pb–Sr isotope homogenized before the mineralization. The Permian flood basalts acted as an impermeable layer for the Pb–Zn mineralization hosted in the Devonian–Carboniferous carbonate rocks.  相似文献   

14.
The Maozu Pb–Zn deposit, located on the western margin of the Yangtze Block, southwest China, is a typical carbonate-hosted deposit in the Sichuan–Yunnan–Guizhou Pb–Zn metallogenic province with Pb + Zn reserves of about 2.0 million tonnes grading 4.15 wt.% Pb and 7.25 wt.% Zn. Its ore bodies are hosted in Sinian (635–541 Ma) Dengying Formation dolostone and show stratiform, vein and irregular textures. Ores are composed of sphalerite, galena, pyrite, calcite, dolomite, quartz and fluorite with massive, banded, disseminated and veined structures. The C–O–Sm–Nd isotopic compositions of hydrothermal calcites and S–Pb isotopic compositions of sulfides were analyzed to constrain the origin of the Maozu deposit. δ13CPDB and δ18OSMOW values of hydrothermal calcites range from −3.7‰ to −2.0‰ and +13.8‰ to +17.5‰, respectively, and plot near the marine carbonate rocks field in a plot of δ13CPDB vs. δ18OSMOW, with a negative correlation. It suggests that CO2 in the hydrothermal fluids was mainly originated from marine carbonate rocks, with limited influence from sedimentary organic matter. δ34SCDT values of sulfides range from +9.9‰ to +19.2‰, similar to that of Cambrian to Triassic seawater sulfate (+15‰ to +35‰) and evaporate (+15‰ to +30‰) in the Cambrian to Triassic sedimentary strata. It suggests that reduced sulfur was derived from evaporate in sedimentary strata by thermo chemical sulfate reduction. Sulfides have low radiogenic Pb isotope compositions (206Pb/204Pb = 18.129–18.375, 207Pb/204Pb = 15.640–15.686 and 208Pb/204Pb = 38.220–38.577) that plot in the field between upper crust and the orogenic belt evolution curve in the plot of 207Pb/204Pb vs. 206Pb/204Pb, and similar to that of age corrected Proterozoic basement rocks (Dongchuan and Kunyang Groups). This indicates that ore-forming metals were mainly derived from basement rocks. Hydrothermal calcite yields a Sm–Nd isotopic age of 196 ± 13 Ma, possibly reflecting the timing of Pb–Zn mineralization in the SYG province, younger than the Permian Emeishan mantle plume (∼260 Ma). All data combined suggests that hydrothermal fluids circulated through basement rocks where they picked up metals and migrated to surface, mixed with reduced sulfur-bearing fluids and precipitated metals. Ore genesis of the Maozu deposit is different from known magmatic–hydrothermal, Sedimentary Exhalative or Mississippi Valley-types, which maybe represent a unique ore deposit type, named as the SYG-type.  相似文献   

15.
The Wulaga gold deposit, located in Heilongjiang province, NE China, is a subvolcanic rock-hosted, low-sulfidation epithermal gold deposit, and has an Au reserve of about 84 tons. The gold mineralization occurs in a crypto-explosive breccia, and is spatially and temporally associated with an Early Cretaceous granodioritic porphyry. Three individual stages of mineralization have been identified in the Wulaga gold deposit: an early white quartz-euhedral vein stage, a fine-grained pyrite–marcasite–stibnite–chalcedony stage, and a late calcite–pyrite stage. The sulfur isotopic values of sulfide minerals vary in a wide range from − 4 to 4.9‰, but are concentrated in the range of − 3 to 0‰, implying that sulfur in the hydrothermal fluids was derived from magmatic volatiles. Lead isotopic results of the granodioritic porphyry (206Pb/204Pb = 18.341–18.395, 207Pb/204Pb = 15.507–15.523, 208Pb/204Pb = 38.174–38.251) and sulfide minerals (206Pb/204Pb = 18.172–18.378, 207Pb/204Pb = 15.536–15.600, 208Pb/204Pb = 38.172–38.339) are comparatively consistent and clustered together between the orogenic and upper mantle lines, indicating the lead in the ores is closely related to the parent magma of the granodioritic porphyry. The REE patterns of fluid inclusions trapped in sulfides are similar to those of the granodioritic porphyry, which confirms the magmatic origin of the REE in the hydrothermal fluids. The characteristics of S and Pb isotopes and REE suggest that the ore-forming materials of the Wulaga gold deposit are partly magmatic in origin, and related to a high-level hydrous granodioritic magma.  相似文献   

16.
The Dapingzhang volcanogenic Cu–Pb–Zn sulfide deposit is located in the Lancangjiang tectonic zone within the Sanjiang region, Yunnan province of southwestern China. The deposit occurs within a felsic volcanic dome belonging to a mid-Silurian volcanic belt stretching for more than 100 km from Dapingzhang to Sandashan. The mineralized volcanic rocks are predominantly keratophyre and quartz keratophyre with subordinate spilite. The Dapingzhang deposit is characterized by well-developed vertical zonation with stockwork ores in the bottom, disseminated sulfide ores in the middle, and massive sulfide ores in the top, overlain by a thin layer of chemical sedimentary exhalative rocks (chert and barite). The Re–Os age of the pyrites from the deposit is 417 ± 23 Ma, indistinguishable from the age of the associated felsic volcanic rocks. The associated felsic volcanic rocks are characterized by negative Nb–Ta anomalies and positive εNd(t) values (+ 4.4–+6.5), similar to the coeval calc-alkaline volcanic rocks in the region. This observation supports the interpretation that the felsic volcanic rocks associated with the Dapingzhang deposit are the derivatives of arc basaltic magma by extensive fractional crystallization. The δ34S values of the sulfides from the deposit vary from − 1.24 to + 4.32‰, indicating a predominantly magmatic source for the sulfur. The sulfides are also characterized by homogeneous and relatively low radiogenic Pb isotope compositions (206Pb/204Pb = 18.310–18.656, 207Pb/204Pb = 15.489–15.643 and 208Pb/204Pb = 37.811–38.662), similar to the Pb isotopic compositions of the associated volcanic rocks. The Pb isotopic data indicate that mantle-derived Pb is more prevalent than crust-derived Pb in the deposit. The S–Pb isotopic data indicate that the important ore-forming materials were mainly derived from the associated volcanic rocks. The δ13CPDB and δ18OSMOW values of the associated hydrothermal calcite crystals vary from − 2.3‰ to + 0.27‰ and from + 14.6 to + 24.4‰, respectively. These values are between the mantle and marine carbonate values. The narrow range of the δ13CPDB values for the calcite indicates that carbon-bearing species in the hydrothermal fluids were primarily derived from marine carbonates. The δ18O values for the hydrothermal fluids, calculated from the measured values for quartz, are between − 2.1‰ and + 3.5‰. The corresponding δD values for the fluids range from − 59‰ to − 84‰. The O–H isotopic data indicate mixing between magmatic fluids and seawater in the ore-forming hydrothermal system. Similar to a typical volcanogenic massive sulfide (VMS) deposit, the ore-forming fluids contained both magmatic fluids and heated seawater; the ore metals and regents were derived from the underlying magma as well as felsic country rocks.  相似文献   

17.
Widespread Mesozoic Au and other hydrothermal polymetal (Zn–Pb–Cu–Mo–Ag–W–Fe–REE) deposits or smaller prospects occur in association with ancient mobile belts surrounding and cutting through the North China Carton (NCC). Among these, the gold ores of the Jiaodong Peninsula, Shandong Province, eastern NCC, represent the largest gold district in China. However, the genesis of these important gold mineralizations has remained controversial, notably their relationships to widespread mafic magmatism of alkaline affinity.The ore bodies of the Guocheng gold deposit on the Jiaodong Peninsula are fracture-controlled, sulfide-rich veins and disseminations, formed contemporaneously with abundant dolerite, lamprophyre and monzonite dikes at ca. 120 Ma. Dolerite dikes possess mantle-like major element compositions and alkaline affinity, associated with prominent subduction-type trace element enrichments. The dikes show petrographic and chemical evidence of magma mixing that triggered exsolution of magmatic sulfide and anhydrite crystallization, preserved as primary inclusions in phenocrysts. LA-ICP-MS analysis of magmatic sulfide inclusions demonstrates that metal abundance ratios (Ag, As, Au, Bi, Co, Cu, Mo, Ni, Pb, Sb, Zn) largely correspond to those of both unaltered bulk rock and bulk ore. Together with identical Pb isotope ratios of dolerite and bulk ore, this demonstrates that gold mineralization and dolerite dikes share a common source.Lead isotope signatures of the ore sulfides are much less radiogenic (17.08 < 206Pb/204Pb < 17.25, 15.41 <207Pb/204Pb < 15.45, 37.55 < 208Pb/204Pb < 37.93) relative to the Pb signature of Phanerozoic convecting mantle and plot to the left of the Geochron and above the MORB-source mantle Pb evolution line. Forward Monte Carlo simulations indicate three events for the U–Th–Pb isotope evolution: (1) late Archean formation of juvenile crust is followed by (2) subduction of this aged crust at ca. 1.85 Ga along with the assembly of Jiao–Liao–Ji mobile belt (suture within Columbia supercontinent). This late-Archean subducted crust released fluids with drastically reduced U/Pb that metasomatized the overlying depleted mantle, which formed cratonic lithospheric mantle. This metasomatized lithospheric mantle was (3) tapped in response to early Cretaceous extensional tectonics affecting notably the eastern margin of the NCC to generate mafic magmas and associated gold mineralization at Guocheng. Similarly non-radiogenic uranogenic Pb isotope data characterize the contemporaneous mafic dikes and gold deposits in the entire Jiaodong Peninsula, suggesting that our genetic model applies to the entire Jiaodong gold district.We propose that early Cretaceous melting of subcontinental lithospheric mantle metasomatized by subduction fluids during Paleoproterozoic amalgamation of terranes to the eastern NCC along with Columbia supercontinent assembly generated mafic magmatism and associated gold deposits. Given the conspicuous association of Phanerozoic hydrothermal ore deposits associated with reactivated Paleoproterozoic mobile belts, we envisage that our genetic model, which largely corresponds to that which is proposed for the Bingham porphyry-Cu–Au–Mo deposit, USA, may explain much of the magmatic-hydrothermal activity and associated ore formation all around the NCC.  相似文献   

18.
The northeastward subduction of the Neo-Tethyan oceanic lithosphere beneath the Iranian block produced vast volcanic and plutonic rocks that now outcrop in central (Urumieh–Dokhtar magmatic assemblage) and north–northeastern Iran (Alborz Magmatic Belt), with peak magmatism occurring during the Eocene. The Karaj Dam basement sill (KDBS), situated in the Alborz Magmatic Belt, comprises gabbro, monzogabbro, monzodiorite, and monzonite with a shoshonitic affinity. These plutonic rocks are intruded into the Karaj Formation, which comprise pyroclastic rocks dating to the lower–upper Eocene. The geochemical and isotopic signatures of the KDBS rocks indicate that they are cogenetic and evolved through fractional crystallization. They are characterized by an enrichment in LREEs relative to HREEs, with negative Nb–Ta anomalies. Geochemical modeling using Sm/Yb versus La/Yb and La/Sm ratios suggests a low-degree of partial melting of a phlogopite–spinel peridotite source to generate the KDBS rocks. Their low ISr = 0.70453–0.70535, ɛNd (37.2 Ma) = 1.54–1.9, and TDM ages ranging from 0.65 to 0.86 Ga are consistent with the melting of a Cadomian enriched lithospheric mantle source, metasomatized by fluids derived from the subducted slab or sediments during magma generation. These interpretations are consistent with high ratios of 206Pb/204Pb = 18.43–18.67, 207Pb/204Pb = 15.59, and 208Pb/204Pb = 38.42–38.71, indicating the involvement of subducted sediments or continental crust. The sill is considered to have been emplaced in an environment of lithospheric extension due to the slab rollback in the lower Eocene. This extension led to localized upwelling of the asthenosphere, providing the heat required for partial melting of the subduction-contaminated subcontinental lithospheric mantle beneath the Alborz magmatic belt. Then, the shoshonitic melt generates the entire spectrum of KDBS rocks through assimilation and fractional crystallization during the ascent of the magma.  相似文献   

19.
Elemental and Sr, Nd, Hf and high precision Pb isotopic data are presented from 59 low-Ti and high-Ti lavas from the syn-break up part of the Faroe Flood Basalt Province. The depleted MORB-like low-Ti lavas erupted in the rift zone between the Faroe Islands and central East Greenland around the time of break up of the North Atlantic have isotopic end-member compositions different from the depleted Iceland lavas. We suggest that the main low-Ti mantle component is NAEM (North Atlantic End-Member (Ellam and Stuart, 2000, J. Petrol. 41, 919) and that the 207Pb/204Pb value of the component should be 15.35 and εHf = + 16.5. NAEM is the main depleted component in the early Iceland plume. This is supported by high mantle potential temperatures (up to 1550 °C) calculated for the source of the low-Ti basalts. The unique mantle isotopic composition of NAEM with low 206Pb/204Pb (17.5) and Δ7/4Pb (? 3.8) precludes a derivation from recycled MORB lithosphere. Instead we suggest that NAEM represents a plume component of recycled depleted Archean lithospheric mantle that was further depleted ~ 500 Ma ago, possibly in connection with the recycling process. Two other isotopic end-members are required to explain the variation of the Faroe low-Ti basalts: (1) The Faroe depleted component (FDC), with 87Sr/86Sr = 0.7025, εNd = + 11, εHf = + 19.5, 206Pb/204Pb = 18.2, 207Pb/204Pb = 15.454 and 208Pb/204Pb = 37.75, which is similar in composition to some Atlantic MORB and is regarded as a local upper mantle source. (2) An enriched EM-type component similar in geochemistry to the Icelandic Öræfajökull lavas. This component is believed to be recycled pelagic sediments in the plume but it can alternatively be a local crustal or lithospheric mantle component. The enriched Faroe high-Ti lavas erupted inland from the rift have isotopic compositions very similar to the enriched Icelandic neo-volcanics and these lava suites apparently share the two enriched plume end-members IE1 and IE2 (Geochim. Cosmochim. Acta 68, 2, 2004). The lack of mixing between high and low-Ti melts at the time of break up, is explained by a zoned plume where only low-Ti sources were present beneath the rift zone surrounded by high-Ti sources on both sides of the rift. The enriched plume components in the high-Ti lava sequences on the Faroe Islands and central East Greenland changed rapidly on a ka-scale which implies, from geophysical modelling, that this area was positioned above the center of the plume, and that the Iceland plume was centered under the Atlantic ridge already from the Paleocene.  相似文献   

20.
Post-collisional, potassic magmatic rocks widely distributed in the eastern Lhasa terrane provide significant information for comprehensive understanding of geodynamic processes of northward subduction of the Indian lithosphere and uplift of the Tibetan Plateau. A combined dataset of whole-rock major and trace elements, Sr–Nd–Pb isotopes, and in situ zircon U–Pb dating and Hf–O isotopic analyses are presented for the Yangying potassic volcanic rocks (YPVR) in the eastern part of the Lhasa terrane, South Tibet. These volcanic rocks consist of trachytes, which are characterized by high K2O (5.46–9.30 wt.%), SiO2 (61.34–68.62 wt.%) and Al2O3 (15.06–17.36 wt.%), and relatively low MgO (0.47–2.80 wt.%) and FeOt (1.70–4.90 wt.%). Chondrite-normalized rare earth elements (REE) patterns display clearly negative Eu anomalies. Primitive mantle-normalized incompatible trace elements diagrams exhibit strong enrichment in large ion lithophile elements (LILE) relative to high field strength elements (HFSE) and display significantly negative Nb–Ta–Ti anomalies. Initial isotopic compositions indicate relatively radiogenic Sr [(87Sr/86Sr)i = 0.711978–0.712090)] and unradiogenic Nd [(143Nd/144Nd)i = 0.512121–0.512148]. Combined with their Pb isotopic compositions [(206Pb/204Pb)i = 18.615–18.774, (207Pb/204Pb)i = 15.708–15.793, (208Pb/204Pb)i = 39.274–39.355)], these data are consistent with the involvement of component from subducted continental crustal sediment in their source region. The whole-rock Sr–Nd–Pb isotopic compositions exhibit linear trends between enriched mantle-derived mafic ultrapotassic magmas and relatively depleted crustal contaminants from the Lhasa terrane. The enrichment of the upper mantle below South Tibet is considered to result from the addition of components derived from subducted Indian continental crust to depleted MORB-source mantle during northward underthrusting of the Indian continental lithosphere beneath the Lhasa terrane since India–Asia collision at ~ 55 Ma. Secondary Ion Mass Spectrometry (SIMS) U–Pb zircon analyses yield the eruptive ages of 10.61 ± 0.10 Ma and 10.70 ± 0.18 Ma (weighted mean ages). Zircon Hf isotope compositions [ƐHf(t) = −4.79 to −0.17], combined with zircon O isotope ratios (5.51–7.22‰), imply an addition of crustal material in their petrogenesis. Clinopyroxene-liquid thermobarometer reveals pressure (2.5–4.1 kbar) and temperature (1029.4–1082.9 °C) of clinopyroxene crystallization, suggesting that depth of the magma chamber was 11.6–16.4 km. Energy-constrained assimilation and fractional crystallization (EC–AFC) model calculation indicates depth of assimilation and fractional crystallization in the region of 14.40–18.75 km underneath the Lhasa terrane, which is in consistent with depth of the magma chamber as suggested by clinopyroxene-liquid thermobarometer. Based on the whole-rock major and trace elements and Sr–Nd–Pb isotope compositions, combined with EC–AFC modeling simulations and zircon Hf–O isotope data, we propose that the YPVR resulted from assimilation and fractional crystallization (AFC) process of the K-rich mafic primitive magmas, which were caused by partial melting of the Indian continental subduction-induced mélange rocks.  相似文献   

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