Metallogeny of the Shilu Fe–Co–Cu deposit,Hainan Island,South China: Constraints from fluid inclusions and stable isotopes

The Shilu deposit is a world-class Fe–Co–Cu orebody located in the Changjiang area of the western part of Hainan Island, South China. The distribution of Fe, Co, and Cu orebodies is controlled by strata of the No. 6 Formation in the Shilu Group and the Beiyi synclinorium. Based on a petrological study of the host rocks and their alteration assemblages, and textural and structural features of the ores, four mineralization stages have been identified: (1) the sedimentary ore-forming period; (2) the metamorphic ore-forming period; (3) the hydrothermal mineralization comprising the skarn and quartz–sulfide stage; and (4) the supergene period. The fluid inclusions in sedimentary quartz and/or chert indicate low temperatures (ca. 160 °C) and low salinities from 0.7 to 3.1 wt.% NaCl_eq, which corresponds to densities of 0.77 to 0.93 g/cm³. CO₂-bearing or carbonic inclusions have been interpreted to result from regional metamorphism. Homogenization temperatures of fluid inclusions for the skarn stage have a wide range from 148 °C to 497 °C and the salinities of the fluid inclusions range from 1.2 to 22.3 wt.% NaCl_eq, which corresponds to densities from 0.56 to 0.94 g/cm³. Fluid inclusions of the quartz–sulfide stage yield homogenization temperatures of 151–356 °C and salinities from 0.9 to 8.1 wt.% NaCl_eq, which equates to fluid densities from 0.63 to 0.96 g/cm³.Sulfur isotopic compositions indicate that sulfur of the sedimentary anhydrite and Co-bearing pyrite, and the quartz–sulfide stage, was derived from seawater sulfate and thermochemical sulfate reduction of dissolved anhydrite at temperatures of 200 °C and 300 °C, respectively. H and O isotopic compositions of the skarn and quartz–sulfide stage demonstrate that the ore-forming fluids were largely derived from magmatic water, with minor inputs from metamorphic or meteoric water. The Shilu iron ore deposit has an exhalative sedimentary origin, but has been overprinted by regional deformation and metamorphism. The Shilu Co–Cu deposit has a hydrothermal origin and is temporally and genetically associated with Indosinian granitoid rocks.     

Geochronology and geochemistry of the Shilu Cu–Mo deposit in the Yunkai area,Guangdong Province,South China and its implication

Shilu is a large porphyry–skarn deposit in the Yunkai district in Guangdong Province, South China. The Shilu granitic intrusion in the mine area is a granodiorite which is genetically related to Cu mineralization. Plagioclase in the granodiorite has a zoned texture and is mainly andesine with minor amounts of labradorite, whereas the K-feldspars exhibit Carlsbad twins and some are also characterized by a zonal texture. K-feldspars from the granodiorite show high contents of Or (87–92 wt.%) with minor Ab (8–13 wt.%) and negligible An value of 0–0.3 wt.%. Biotite can be classified as magnesio-biotite, and is characterized by Mg-rich [Mg/(Mg + Fe) = 0.54–0.60] and Al^VI-low (average values = 0.11). Hornblende is chiefly magnesiohornblende and tschermakite. LA-ICP-MS zircon U–Pb age of the Shilu granodiorite is 107 ± 0.7 Ma, which is consistent with molybdenites Re–Os age of 104.1 ± 1.3 Ma. Geochemical data indicate that the Shilu granodiorite is silica-rich (SiO₂ = 63.43–65.03 wt.%) and alkali-rich (K₂O + Na₂O = 5.45–6.05 wt.%), as well as calcium-rich (CaO = 4.76–5.1 wt.%). Trace element geochemistry results show enrichments in large ion lithophile elements (e.g., Rb, K, and Ba) and depletions in some high field strength elements (e.g., Nb, P, Ta, and Ti). The total rare earth element (REE) content of the granodioritic rocks is low (∑ REE < 200 ppm), and is characterized by light REE enrichment [(La/Yb)_N > 9] and moderately negative Eu anomalies (Eu/Eu* = 0.83–0.90). These mineralogical, geochronological, and geochemical results suggest that the Shilu granodiorite has a mixed crust–mantle source with a geochemical affinity to I-type granitoids. Hornblende thermobarometry yielded magmatic crystallization temperatures of 686–785 °C and crystallization pressures between 1.0 and 2.34 kbar, which is converted to depths in a range of 3.31 to 7.71 km. Biotite thermobarometry yielded similar temperatures and lower pressures of 680–780 °C and 0.8–2 kbar (depth 2.64–6.6 km), respectively. The parent magma had a high oxygen fugacity. The Shilu granodiorite has a relatively low ε_Nd/t–t value and high (⁸⁷Sr/⁸⁶Sr)_i value, and Nd isotopes yield two-stage depleted mantle Nd model ages of 969–1590 Ma. Our new data, combined with previous studies, imply that the granodiorite and the associated Shilu Cu–Mo deposit was formed in an extensional environment, closely related to remelting of residual subducted slab fragments in the Jurassic.     

Copper isotopic compositions of the Zijinshan high-sulfidation epithermal Cu–Au deposit,South China: Implications for deposit origin

The Zijinshan high-sulfidation epithermal Cu–Au deposit is located in the Zijinshan ore field of South China, comprising porphyry–epithermal Cu–Au–Mo–Ag ore systems. The Cu ore body is more than 1000 m thick and is characterized by an assemblage of digenite–covellite–enargite–alunite. Digenite is the dominant Cu-bearing mineral, which makes this deposit unique, although the mechanisms of digenite formation remain controversial. To elucidate the genesis of digenite, this paper presents the Cu isotopic compositions of Cu-sulfides in the Zijinshan high-sulfidation Cu–Au deposit. The Cu isotopic values (⁶⁵Cu relative to NIST 976) of all samples range from −2.97‰ to +0.34‰, and most values fall in a narrow range from −0.49‰ to +0.34‰, which is similar to the Cu isotopic signature of typical porphyry systems. Copper isotope ratios of each mineral decrease with increasing depth, a trend that is also typical of porphyry deposits. The variation tendency of δ⁶⁵Cu values between sulfides is consistent with the sequence of mineral formation. These observations suggest that the Cu-sulfides in the Zijinshan Cu–Au deposit have a hypogene origin.     

Geological,fluid inclusion and isotopic studies of the Yinshan Cu–Au–Pb–Zn–Ag deposit,South China: Implications for ore genesis and exploration

The Yinshan Cu–Au–Pb–Zn–Ag deposit is located in Dexing, South China. Ore bodies are primarily hosted in low-grade phyllite of the Neoproterozoic Shuangqiaoshan Group along EW- and NNW-striking fault zones. Pb–Zn–Ag mineralization is dictated by Jurassic rhyolitic quartz porphyries (ca. 172 Ma), whereas Cu–Au mineralization is associated with Jurassic dacite porphyries (ca. 170 Ma). The main ore minerals are pyrite, chalcopyrite, galena, sphalerite, tetrahedrite–tennatite, gold, silver, and silver sulphosalt, and the principal gangue minerals are quartz, sericite, calcite, and chlorite. Two-phase liquid-rich (type I), two-phase vapor-rich (type II), and halite-bearing (type III) fluid inclusions can be observed in the hydrothermal quartz-sulfides veins. Type I inclusions are widespread and have homogenization temperatures of 187–303 °C and salinities of 4.2–9.5 wt.% NaCl equivalent in the Pb–Zn–Ag mineralization, and homogenization temperatures of 196–362 °C and salinities of 3.5–9.9 wt.% NaCl equivalent in the Cu–Au mineralization. The pervasive occurrence of type I fluid inclusions with low-moderate temperatures and salinities implies that the mineralizing fluids formed in epithermal environments. The type II and coexisting type III inclusions, from deeper levels below the Cu–Au ore bodies, share similar homogenization temperatures of 317–448 °C and contrasting salinities of 0.2–4.2 and 30.9–36.8 wt.% NaCl equivalent, respectively, which indicates that boiling processes occurred. The sulfur isotopic compositions of sulfides (δ³⁴S = −1.7‰ to +3.2‰) suggest a homogeneous magmatic sulfur source. The lead isotopes of sulfides (²⁰⁶Pb/²⁰⁴Pb = 18.01–18.07; ²⁰⁷Pb/²⁰⁴Pb = 15.55–15.57; and ²⁰⁸Pb/²⁰⁴Pb = 38.03–38.12) are consistent with those of volcanic–subvolcanic rocks (²⁰⁶Pb/²⁰⁴Pb = 18.03–18.10; ²⁰⁷Pb/²⁰⁴Pb = 15.56–15.57; and ²⁰⁸Pb/²⁰⁴Pb = 38.02–38.21), indicating a magmatic origin for lead in the ore. The oxygen and hydrogen isotope compositions (δ¹⁸O = +7.8‰ to +10.5‰, δD = −66‰ to −42‰) of inclusion water in quartz imply that ore-forming fluids were mainly derived from magmatic sources. The local boiling process beneath the epithermal Cu–Au ore-forming system indicates the possibility that porphyry-style ore bodies may exist at even deeper zones.     

Zircon and molybdenite geochronology and geochemistry of the Kalmakyr porphyry Cu–Au deposit,Almalyk district,Uzbekistan: Implications for mineralization processes

Copper, gold and molybdenum mineralization of the Kalmakyr porphyry deposit in Uzbek Tien Shan occurs as stockworks, veinlets and disseminations in the phyllic and K-silicate alteration zones developed predominantly in a middle to late Carboniferous intrusive complex composed of monzonite and granodiorite porphyry. Zircon U–Pb dating yielded an age of 327.2 ± 5.6 Ma for the ore-hosting monzonite and an age of 313.6 ± 2.8 Ma for the ore-bearing granodiorite porphyry. Re–Os dating of seven molybdenite samples from stockwork and veinlet ores yielded model ages from 313.2 to 306.3 Ma, with two well-constrained isochron ages of 307.6 ± 2.5 Ma (five stockwork ores) and 309.1 ± 2.2 Ma (five stockwork ores and two veinlet ores), respectively. These results indicate that Cu–Au mineralization post-dated the emplacement of the monzonite, started right after the emplacement of the granodiorite porphyry, and lasted for ca. 7 Ma afterward. The geochronological and geochemical data suggest that the Kalmakyr deposit was formed in a late Carboniferous mature magmatic arc setting, probably related to the latest subduction process of the Turkestan Ocean beneath the Middle Tien Shan. The ε_Hf(t) values of zircon grains from the monzonite vary from +11 to +1.7, with an average of +5.1, and those of zircon grains from the granodiorite porphyry range from +5.7 to −1.8, with an average of +2.4. These data indicate that the magma of both monzonite and granodiorite porphyry was derived from partial melting of a thickened lower crust with input of mantle components and variable crustal contamination, and that there was more mantle contribution to the formation of the monzonite than the granodiorite porphyry. The high rhenium concentrations of molybdenite (98–899 ppm) also indicate major mantle contribution of rhenium and by inference ore metals. The relatively high Eu_N/Eu_N¹ values (average 0.68), Ce⁴⁺/Ce³ values (average 890) and Ce/Nd values (average 36.8) for zircon grains from the granodiorite porphyry than those from the monzonite (average Eu_N/Eu_N¹ = 0.33, average Ce⁴⁺/Ce³ = 624, average Ce/Nd = 3.9) suggest that the magma for the syn-mineralization granodiorite porphyry has higher oxygen fugacity than that for the pre-mineralization monzonite. Based on these data, it is proposed that while the monzonite was emplaced, the oxygen fugacity and volatile contents in the magma were relatively low, and ore metals might disperse in the intrusive rock, whereas when the granodiorite porphyry was emplaced, the oxygen fugacity and volatile contents in the magma were increased, favoring copper and gold enrichment in the magmatic fluids. The Kalmakyr deposit formed from a long-lived magmatic-hydrothermal system connected with fertile magmatic sources in relation to the subduction of the Turkestan Ocean beneath the Middle Tien Shan.     

Geochronology and geochemistry of Cretaceous Nanshanping alkaline rocks from the Zijinshan district in Fujian Province,South China: Implications for crust–mantle interaction and lithospheric extension

In situ zircon U–Pb ages and Hf isotopic data, major and trace elements, and Sr–Nd–Pb isotopic compositions are reported for Nanshanping alkaline rocks from the Zijingshan district in southwestern Fujian Province (the Interior or Western Cathaysia Block) of South China. The Nanshanping alkaline rocks, which consist of porphyritic quartz monzonite, porphyritic syenite, and syenite, revealed a Late Cretaceous age of 100–93 Ma. All of the rocks show high SiO₂, K₂O + Na₂O, and LREE but low CaO, Fe₂O₃^T, MgO, and HFSE (Nb, Ta, P, and Ti) concentrations. These rocks also exhibit uniform initial ⁸⁷Sr/⁸⁶Sr ratios of 0.7078 to 0.7087 and ε_Nd(t) values of −4.1 to −7.2, thus falling within the compositional field of Cretaceous basalts and mafic dikes occurring in the Cathaysia Block. Additionally, these rocks display initial Pb isotopic compositions with a ²⁰⁶Pb/²⁰⁴Pb_i ratio of 18.25 to 18.45, a ²⁰⁷Pb/²⁰⁴Pb_i ratio of 15.63 to 15.67, and a ²⁰⁸Pb/²⁰⁴Pb_i ratio of 38.45 to 38.88. Combined with the zircon Hf isotopic compositions (ε_Hf(t) = −11.7 to −3.2), which are different from those of the basement rocks, we suggest that Nanshanping alkaline rocks were primarily derived from a subduction-related enriched mantle source. High Rb/Sr (0.29–0.65) and Zr/Hf (37.5–49.2) but relatively low Ba/Rb (4.4–8.1) ratios suggest that the parental magmas of these rocks were most likely formed via partial melting of a phlogopite-bearing mantle source with carbonate metasomatism. The relatively high SiO₂ (62.35–70.79 wt.%) and low Nb/Ta (10.0–15.3) ratios, positive correlation between SiO₂ and (⁸⁷Sr/⁸⁶Sr)_I, and negative correlation between SiO₂ and ε_Nd(t) of these rocks suggest that the crustal materials were also involved in formation of the Nanshanping alkaline rocks. Combined with geochemical and isotopic features, we infer magmatic processes similar to AFC (assimilation and fractional crystallization) involving early fractionation of clinopyroxene and olivine and subsequent fractionation of biotite-dominated assemblages coupled with a lesser amount of crustal contamination, thereby forming the Nanshanping alkaline rocks. The Nanshanping alkaline rocks appear to be associated with an extensional environment in the Cathaysia Block. This extensional regime could have resulted in the slab break-off and rollback of the subducting paleo-Pacific plate and the upwelling of the asthenospheric mantle, which induced partial melting of the enriched lithospheric mantle in the Cretaceous.     

Magnetite geochemistry of the Longqiao and Tieshan Fe–(Cu) deposits in the Middle-Lower Yangtze River Belt: Implications for deposit type and ore genesis

Magnetite is a common mineral in many ore deposits and their host rocks, and contains a wide range of trace elements (e.g., Ti, V, Mg, Cr, Mn, Ca, Al, Ni, Ga, Sn) that can be used for deposit type fingerprinting. In this study, we present new magnetite geochemical data for the Longqiao Fe deposit (Luzong ore district) and Tieshan Fe–(Cu) deposit (Edong ore district), which are important magmatic-hydrothermal deposits in eastern China.Textural features, mineral assemblages and paragenesis of the Longqiao and Tieshan ore samples have suggested the presence of two main mineralization periods (sedimentary and hydrothermal) at Longqiao, among which the hydrothermal period comprises four stages (skarn, magnetite, sulfide and carbonate); whilst the Tieshan Fe–(Cu) deposit comprises four mineralization stages (skarn, magnetite, quartz-sulfide and carbonate).Magnetite from the Longqiao and Tieshan deposits has different geochemistry, and can be clearly discriminated by the Sn vs. Ga, Ni vs. Cr, Ga vs. Al, Ni vs. Al, V vs. Ti, and Al vs. Mg diagrams. Such difference may be applied to distinguish other typical skarn (Tieshan) and multi-origin hydrothermal (Longqiao) deposits in the MLYRB. The fluid–rock interactions, influence of the co-crystallizing minerals and other physicochemical parameters, such as temperature and fO₂, may have altogether controlled the magnetite trace element contents of both deposits. The Tieshan deposit may have had higher degree of fO₂, but lower fluid–rock interactions and ore-forming temperature than the Longqiao deposit. The TiO₂–Al₂O₃–(MgO + MnO) and (Ca + Al + Mn) vs. (Ti + V) magnetite discrimination diagrams show that the Longqiao Fe deposit has both sedimentary and hydrothermal features, whereas the Tieshan Fe–(Cu) deposit is skarn-type and was likely formed via hydrothermal metasomatism, consistent with the ore characteristics observed.     

Electron microprobe analyses of ore minerals and H–O,S isotope geochemistry of the Yuerya gold deposit,eastern Hebei,China: Implications for ore genesis and mineralization

The Yuerya gold deposit in eastern Hebei Province, China, is located on the eastern margin of the North China Craton and is hosted by Mesozoic Yanshanian granitoid rocks and adjacent Mesoproterozoic Gaoyuzhuang Formation carbonates. The auriferous quartz veins in this deposit are dominated by pyrite, with subordinate sphalerite, chalcopyrite, and galena in a quartz-dominated gangue that also contains calcite, dolomite, barite, apatite, and fluorite. Gold is present as native gold and electrum, which are generally present as micron-size infillings in microfissures within pyrite and less commonly as tiny inclusions within pyrite, quartz, and tellurobismuthite. The pyrite in this deposit has high Co/Ni ratios and contains elevated concentrations of both of these elements, suggesting that the Yuerya gold deposit has a magmato-hydrothermal origin and that the ore-forming fluids that formed the deposit leached trace elements such as Co, Ni, As, and Au during passage through Archean metamorphic rocks, Mesoproterozoic carbonates, and the Yanshanian Yuerya granitoid. Pyrite in the study area has S/Se ratios and S isotopic compositions that suggest that the sulfur (and by inference the gold) within the deposit was sourced from magmato-hydrothermal fluids that were probably originally derived from Archean metamorphic rocks and Yanshanian granitoids. Tellurobismuthite in the study area is closely intergrown with gold and was the single telluride phase identified during this study. The fineness of gold associated with tellurobismuthite is greater than the fineness of gold associated with pyrite, although the fine particle size of the gold surrounded by tellurobismuthite means that the recovery of this gold is difficult, in turn meaning that the tellurobismuthite has little significance to the economics of the Yuerya gold deposit. Only trace amounts of sulfides are associated with the tellurobismuthite within the Yuerya gold deposit, suggesting that this mineral was deposited under conditions of low fS₂ and/or high fTe₂. In addition, the presence of tellurides within the Yuerya gold deposit reflects a genetic relationship between the deposit and magmatism. Quartz from mineralized veins in the study area has δ¹⁸O values of 11.2‰–12.9‰ and the fluids that formed these veins have δD values of − 78.3‰ to − 72.1‰. The δ³⁴S values of pyrite within the deposit are rather restricted (2.3‰–3.5‰). These data, combined with the trace element geochemistry of sulfides within the deposit, suggest that the formation of the Yuerya gold deposit was closely related to both Archean metamorphic rocks and the Yanshanian Yuerya granitoid.     

Sm–Nd geochronology and geochemistry of a Neoproterozoic gabbro in the Kuluketage block,north-western China

In this article, we report whole-rock and mineral Sm–Nd isotopic and whole-rock elemental and Sr–Nd isotopic data of Xingdi No. 1 mafic–ultramafic intrusion in the western Kuluketage block, north-eastern Tarim. Xingdi No. 1 mafic–ultramafic intrusion is the largest in the Xingdi mafic–ultramafic belt, with an exposed area of ca. 20 km². It intruded into the Palaeoproterozoic basement. Gabbro is the major rock type and there is minor olivine pyroxenite. Sm–Nd geochronometry of the gabbro gives an isochron age of 761.2 ± 31.2 million years, identical to the intrusive age of Xingdi No. 2 pluton (760 ± 6 million years). The gabbro is systematically enriched in large ion lithosphile elements and light rare earth elements and depleted in high field strength elements and heavy rare earth elements. The studied rocks are characterized by low whole-rock and mineral ?Nd_(t) values (?7.8 to??7.1) and elevated (⁸⁷Sr/⁸⁶Sr) _i values (0.7066–0.7073). These geochemical characteristics, together with the presence of abundant hornblende, biotite, bladed biotite enclosed in amphibole, and crescent-shaped Palaeoproterozoic wall-rock xenoliths in the intrusion, are key features of magma mixing in the source or assimilation during its emplacement. The rocks have a Zr/Y ratio of 3.81–13, which falls in the within-plate basalt area. As Xingdi No. 1 and No. 2 plutons formed at the same period and display similar geochemical characteristics, we propose that they formed within the same tectonic setting and were derived from the same source, but No. 1 pluton experienced a higher extent of evolution and contamination. Previous studies have shown that the Neoproterozoic tectonic and magmatic events in Kuluketage comprise syn-collisional granite around TC (ca. 1.0–0.9 Ga), post-collisional K-rich granite and alkaline mafic–ultramafic intrusions (ca. 830–800 Ma), and rifting-related mafic–ultramafic plutons, dikes, and bimodal volcanic rocks (ca. 774–744 Ma).     

Geology and geochemistry of the Mammoth breccia pipe,Copper Creek mining district,southeastern Arizona: evidence for a magmatic–hydrothermal origin

The Copper Creek mining district, southeastern Arizona, contains more than 500 mineralized breccia pipes, buried porphyry-style, copper-bearing stockworks, and distal lead–silver veins. The breccia pipes are hosted by the Copper Creek Granodiorite and the Glory Hole volcanic rocks. The unexposed Mammoth breccia pipe, solely recognized by drilling, has a vertical extent of 800 m and a maximum width of 180 m. The pipe consists of angular clasts of granodiorite cemented by quartz, chalcopyrite, bornite, anhydrite, and calcite. Biotite ⁴⁰Ar/³⁹Ar dates suggest a minimum age of 61.5 ± 0.7 Ma for the host Copper Creek Granodiorite and ⁴⁰Ar/³⁹Ar dates on hydrothermal sericite indicate an age of 61.0 ± 0.5 Ma for copper mineralization. Fluid inclusion studies suggest that a supercritical fluid with a salinity of approximately 10 wt.% NaCl equiv. condensed to a dilute aqueous vapor (1–2.8 wt.% NaCl equiv.) and a hypersaline brine (33.4–35.1 wt.% NaCl equiv.). Minimum trapping temperatures are 375°C and trapping depths are estimated at 2 km. Sulfur isotope fractionation of cogenetic anhydrite and chalcopyrite yields a temperature of mineralization of 469 ± 25°C. Calculated oxygen and hydrogen isotope values for fluids in equilibrium with quartz and sericite range from 10.2‰ to 13.4‰ and −60‰ to −39‰, respectively, suggesting that the mineralizing fluid was dominantly magmatic. Evidence from the stable isotope and fluid inclusion analyses suggests that the fluids responsible for Cu mineralization within the Mammoth breccia pipe exsolved from a gray porphyry phase found at the base of the breccia pipe.     

Geodynamic setting of the Zijinshan porphyry–epithermal Cu–Au–Mo–Ag ore system,SW Fujian Province,China: Constrains from the geochronology and geochemistry of the igneous rocks

Zijinshan is a large porphyry–epithermal Cu–Au–Mo–Ag ore system located in the Zijinshan mineral field (ZMF) of southwestern Fujian Province, China. Although it is commonly accepted that the early Cretaceous magmatism and the metallogenesis of the mineral field are closely related, the tectonic setting for the ore-forming event(s) has been controversial and regarded as either extensional or subduction-related. New U–Pb zircon geochronology, Sr–Nd–Pb isotopic systematics, and geochemical data presented here from granites and volcanic rocks in the mineral field help to clarify this uncertainty.LA–MC–ICP-MS U–Pb zircon analyses yield weighted mean ages of between ca. 165 and 157 for the monzogranite, ca. 112 Ma for granodiorite, and between ca. 111 and 102 Ma for nine samples of volcanic units in the study area. These dates, integrated with previous geochronological data, indicate that there were two magmatic events in the area during the Middle to Late Jurassic and the Early Cretaceous. Major and trace element geochemistry indicates that these rocks are high-K, calc-alkaline granites, are enriched in LREE and Th, U, Ta, Nd, Sm and Yb, and depleted in Ba, K, Sr, P, Ti and Y. These features are characteristic of volcanic-arc granites or active-continental margin granites. The Middle to Late Jurassic monzogranitic plutons in the region have initial ⁸⁷Sr/⁸⁶Sr ratios of 0.7096 to 0.7173, εNd_T values of − 10.1 to − 7.6, ²⁰⁶Pb/²⁰⁴Pb isotope ratios of 18.51–18.86, ²⁰⁷Pb/²⁰⁴Pb isotope ratios of 15.64–15.73, and ²⁰⁸Pb/²⁰⁴Pb isotope ratios of 38.76–39.18. The Early Cretaceous granodiorite and volcanic rocks are distinctly different with initial ⁸⁷Sr/⁸⁶Sr ratios of 0.7055–0.7116, εNd_T values of − 8 to 0.5, ²⁰⁶Pb/²⁰⁴Pb ratios ranging between 18.49 and 19.77, ²⁰⁷Pb/²⁰⁴Pb ratios of 15.63–15.71, and ²⁰⁸Pb/²⁰⁴Pb ratios of 38.71–40.62. These characteristics suggest that the source for the Middle to Late Jurassic monzogranitic plutons is a partially melted Mesoproterozoic substrate, with a minor component from Paleozoic material, whereas the Early Cretaceous granodiorite and volcanic rocks may represent mixing of crustal and mantle-derived melts. It is therefore suggested that the Middle to Late Jurassic monzogranitic plutons, and the Early Cretaceous granodiorite and volcanic rocks in the ZMF are the result of an active continental-margin setting related to the subduction of the Paleo-Pacific Plate beneath the Eurasian continent. Given that the mineralization and the early Cretaceous granodiorite and volcanic rocks in the area are genetically related, the Zijinshan porphyry–epithermal ore system formed in the subduction-related tectonic setting.     

Alteration and ore distribution in the Proterozoic Mines Series, Tenke-Fungurume Cu–Co district, Democratic Republic of Congo

Two sediment-hosted stratiform Cu–Co deposits in the Tenke-Fungurume district of the Central African Copperbelt were examined to evaluate the alteration history of the ore-hosting Mines Series and its implications for ore distribution and processing. Core logging and petrography, focused on lithology and timing relationships, outlined a complex alteration sequence whose earliest features include formation of anhydrite nodules and laths, followed by precipitation of dolomite. Later alteration episodes include at least two silica introductions, accompanied by or alternating with two dolomite introductions into the existing gangue assemblages. One introduction of Cu–Co sulfides accompanied the last episode of dolomite alteration, overprinting an earlier generation of ore whose gangue association was unidentifiable. Sulfides and some carbonates were subsequently modified by supergene oxidation, transport, and reprecipitation to 100–200?m depth. Present-day ore distribution resulted from these successive processes. Ore is concentrated in two shale-dominated units on either side of a cavernous silicified dolomite, which is interpreted as the main conduit for the mineralizing fluids. Sulfide ores precipitated at the redox or sulfidation contacts between this dolomite and the shales. Later, supergene fluids dissolved and moved some of the metals, redepositing them as oxides and carbonates. Solubility differences between Cu and Co in supergene conditions caused them to precipitate separately. Thus, modern ore distribution at Tenke-Fungurume results both from original hypogene lithology- and contact-related precipitation and from supergene oxidation, transport, and Cu–Co decoupling. The supergene fluid flow also redistributed gangue minerals such as dolomite, which has an economically important influence on the processing costs of supergene ores.     

The origin of the Dapingzhang volcanogenic Cu–Pb–Zn ore deposit,Yunnan province,SW China: Constraints from host rock geochemistry and ore Os–Pb–S–C–O–H isotopes

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 ε_Nd(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 δ¹³C_PDB and δ¹⁸O_SMOW 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 δ¹³C_PDB 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.     

Isotope geochemistry of ore fluids for the Dongsheng sandstone-type uranium deposit, China

The Dongsheng sandstone-type uranium deposit is one of the large-sized sandstone-type uranium deposits discovered in the northern part of the Ordos Basin of China in recent years. Geochemical characteristics of the Dongsheng uranium deposit are significantly different from those of the typical interlayered oxidized sandstone-type uranium ore deposits in the region of Middle Asia. Fluid inclusion studies of the uranium deposit showed that the uranium ore-forming temperatures are within the range of 150–160℃. Their 3He/4He ratios are within the range of 0.02–1.00 R/Ra, about 5–40 times those of the crust. Their 40Ar/36Ar ratios vary from 584 to 1243, much higher than the values of atmospheric argon. The δ18OH2O and δD values of fluid inclusions from the uranium deposit are -3.0‰– -8.75‰ and -55.8‰– -71.3‰, respectively, reflecting the characteristics of mixed fluid of meteoric water and magmatic water. The δ18OH2O and δD values of kaolinite layer at the bottom of the uranium ore deposit are 6.1‰ and -77‰, respectively, showing the characteristics of magmatic water. The δ13CV-PDB and δ18OH2O values of calcite veins in uranium ores are -8.0‰ and 5.76‰, respectively, showing the characteristics of mantle source. Geochemical characteristics of fluid inclusions indicated that the ore-formation fluid for the Dongsheng uranium deposit was a mixed fluid of meteoric water and deep-source fluid from the crust. It was proposed that the Jurassic-Cretaceous U-rich metamorphic rocks and granites widespread in the northern uplift area of the Ordos Basin had been weathered and denudated and the ore-forming elements, mainly uranium, were transported by meteoric waters to the Dongsheng region, where uranium ores were formed. Tectonothermal events and magmatic activities in the Ordos Basin during the Mesozoic made fluids in the deep interior and oil/gas at shallow levels upwarp along the fault zone and activated fractures, filling into U-bearing clastic sandstones, thus providing necessary energy for the formation of uranium ores.     

U–Pb and Ar–Ar geochronology of the Fujiawu porphyry Cu–Mo deposit,Dexing district,Southeast China: Implications for magmatism,hydrothermal alteration,and mineralization

The Fujiawu porphyry Cu–Mo deposit is one of several porphyry Cu–Mo deposits in the Dexing district, Jiangxi Province, Southeast China. New zircon SHRIMP U–Pb data yield a weighted mean ²⁰⁶Pb/²³⁸U age of 172.0 ± 2.1 and 168.5 ± 1.4 Ma from weakly altered granodiorite porphyry and quartz diorite porphyry, respectively. Two hydrothermal biotites from granodiorite porphyry give an Ar–Ar step-heating plateau age of 169.9 ± 1.8 and 168.7 ± 1.8 Ma. Hydrothermal apatite exsolved from altered biotite yields an isotope dilution thermal ionization mass spectrometry isochron age of 164.4 ± 0.9 Ma. The apatite age is similar to the ages obtained from hydrothermal rutile (165.0 ± 1.1 and 164.8 ± 1.6 Ma) and indicates that the magmatism and hydrothermal activity in the Fujiawu deposit occurred in the Middle Jurassic. Hydrothermal fluid circulation related to multiple stages of magma emplacement resulted in Cu–Mo mineralization in the Fujiawu porphyry deposit. The zircon SHRIMP U–Pb ages and the published molybdenite Re–Os age (170.9 ± 1.5 Ma) represent the timing of magma crystallization and Mo mineralization, whereas the rutile and apatite U–Pb ages reflect the timing of Cu mineralization following quartz diorite emplacement. The data suggest slow cooling after emplacement of the quartz diorite porphyry.     

Geochronology and Hf–Fe isotopic geochemistry of the Phanerozoic mafic–ultramafic intrusions in the Damiao area,northern North China Craton: Implications for lithospheric destruction

Timing and source of several Fe-mineralized mafic-ultramaficintrusions in the Damiao area are investigated here by coupling new geochronological and Hf–Fe isotopic data with previous results. Although regarded as a Late Paleoproterozoic assemblage previously, two ～140 Ma intrusions are recognized by zircon U–Pb dating, indicating emplacement of these intrusions from Middle Devonian to Early Cretaceous times. Both Hf and Fe isotopic features lead to the conclusion that distinct mantle components contributed to their magma generation. As the first magmatic phase, the ～395 Ma intrusions were mainly derived from the slightly-enriched SCLM that was prevalent during the Paleozoic. However, asthenospheric material was strongly involved in the formation of the ～215 Ma Gaositai intrusion. Therefore, the initiation of lithospheric destruction in the northern NCC is inferred to have occurred in Late Triassic time, triggered by post-orogenic extension following the ～250 Ma collision between the Siberian Craton and the NCC. The ～140 Ma intrusions originated from a significantly-enriched mantle component probably resided in the predominant slightly-enriched SCLM. This mantle source would have melted in the Late Mesozoic, when the thin lithosphere enabled enhanced heat transfer from the asthenosphere. In summary, these distinct mantle sources of mafic–ultramafic magmatism provide a record of mantle heterogeneity and the gradual upward migration of the lithosphere–asthenosphere boundary during lithospheric destruction.     

Age and geochemistry of the Neoproterozoic granitoids in the the Songnen–Zhangguangcai Range Massif, NE China: Petrogenesis and tectonic implications

<正>1 Introduction The Songnen–Zhangguangcai Range Massif(SZRM)crops out over an extensive part of NE China and was thought to contain Precambrian crystalline basement material,as evidenced by the presence of what appears to bePaleoproterozoicbasementmaterialwithin exploration drillholes(Pei et al.,2007).An alternative view is that the basement within the SZRM is     

Evolution of the magmatic–hydrothermal system and formation of the giant Zhuxi W–Cu deposit in South China

The Zhuxi deposit is a recently discovered W–Cu deposit located in the Jiangnan porphyry–skarn W belt in South China. The deposit has a resource of 3.44 million tonnes of WO3, making it the largest on Earth,however its origin and the evolution of its magmatic–hydrothermal system remain unclear, largely because alteration–mineralization types in this giant deposit have been less well-studied, apart from a study of the calcic skarn orebodies. The different types of mineralization can be classified into magnesian skarn, calcic skarn, and scheelite–quartz–muscovite(SQM) vein types. Field investigations and mineralogical analyses show that the magnesian skarn hosted by dolomitic limestone is characterized by garnet of the grossular–pyralspite(pyrope, almandine, and spessartine) series, diopside, serpentine,and Mg-rich chlorite. The calcic skarn hosted by limestone is characterized by garnet of the grossular–andradite series, hedenbergite, wollastonite, epidote, and Fe-rich chlorite. The SQM veins host highgrade W–Cu mineralization and have overprinted the magnesian and calcic skarn orebodies. Scheelite is intergrown with hydrous silicates in the retrograde skarn, or occurs with quartz, chalcopyrite, sulfide minerals, fluorite, and muscovite in the SQM veins.Fluid inclusion investigations of the gangue and ore minerals revealed the evolution of the ore-forming fluids, which involved:(1) melt and coexisting high–moderate-salinity, high-temperature, high-pressure(>450 ℃and >1.68 kbar), methane-bearing aqueous fluids that were trapped in prograde skarn minerals;(2) moderate–low-salinity, moderate-temperature, moderate-pressure(~210–300 ℃and ~0.64 kbar),methane-rich aqueous fluids that formed the retrograde skarn-type W orebodies;(3) low-salinity,moderate–low-temperature, moderate-pressure(~150–240 ℃and ~0.56 kbar), methane-rich aqueous fluids that formed the quartz–sulfide Cu(–W) orebodies in skarn;(4) moderate–low-salinity,moderate-temperature, low-pressure(~150–250 ℃and ~0.34 kbar) alkanes-dominated aqueous fluids in the SQM vein stage, which led to the formation of high-grade W–Cu orebodies. The S–Pb isotopic compositions of the sulfides suggest that the ore-forming materials were mainly derived from magma generated by crustal anatexis, with minor addition of a mantle component. The H–O isotopic compositions of quartz and scheelite indicate that the ore-forming fluids originated mainly from magmatic water with later addition of meteoric water. The C–O isotopic compositions of calcite indicate that the ore-forming fluid was originally derived from granitic magma, and then mixed with reduced fluid exsolved from local carbonate strata. Depressurization and resultant fluid boiling were key to precipitation of W in the retrograde skarn stage. Mixing of residual fluid with meteoric water led to a decrease in fluid salinity and Cu(–W) mineralization in the quartz–sulfide stage in skarn. The high-grade W–Cu mineralization in the SQM veins formed by multiple mechanisms, including fracturing, and fluid immiscibility, boiling, and mixing.