Noble Gas and Stable Isotopic Constraints on the Origin of the Ag–Cu Polymetallic Ore Deposits in the Baiyangping Area,Yunnan Province,SW China

The Lanping basin, Yunnan province, SW China, is located at the juncture of the Eurasian and Indian Plates in the eastern part of the Tibetan Plateau. The Lanping basin, in the Sanjiang Tethyan metallogenic province, is a significant Cu–Ag–Zn–Pb mineralized belt in China that includes the largest sandstone‐hosted Zn–Pb deposit in the world, the Jinding deposit, as well as several Ag–Cu deposits (the Baiyangping and Jinman deposits). These deposits, with total reserves of over 16.0 Mt Pb + Zn, 0.6 Mt Cu, and 7,000 t Ag, are mainly hosted in Meso‐Cenozoic clastic rocks and are dominantly controlled by two Cenozoic thrust systems developed in the western and eastern segments of the basin. The Baiyangping, Babaoshan, and Hetaoqing ore deposits are representative of the epithermal base metal deposits in the Lanping basin. The microthermometric data show that the ore‐forming fluids for these deposits were low temperature (110–180 °C) and had bimodal distribution of salinity at moderate and mid to high salinities (approximately 2–8 wt.% and 18–26 wt.% NaCl equivalent). The C and O isotope data indicate that the ore‐forming fluids were related to hot basin brines. We present new He and Ar isotope data on volatiles released from fluid inclusions contained in sulfides and in barite in these three deposits. ³He/⁴He ratios of the ore‐forming fluids are 0.01 to 0.14 R/Ra with a mean of 0.07 Ra (where R is the ³He/⁴He ratio and Ra is the ratio for atmospheric helium). This mean value is intermediate to typical ³He/⁴He ratios for the crust (R/Ra = 0.01 to 0.05) and the ratio for air‐saturated water (R/Ra = 1). The mean ratio is also significantly lower than the ratios found for mantle‐derived fluids (R/Ra = 6 to 9). The ⁴⁰Ar/³⁶Ar ratios of the ore‐forming fluids range from 298 to 382 with a mean of 323. This value is slightly higher than that for the air‐saturated water (295.5). The ³He/⁴He ratios of fluids from the fluid inclusions imply that the ore‐forming fluid for the Baiyangping, Babaoshan, and Hetaoqing deposits was derived from the crust and that any mantle‐derived He was negligible. The content of the radiogenic Ar ranges between 0.2 to 20.4%, and the proportion of air‐derived ⁴⁰Ar averages 94.1%. This indicates that atmospheric Ar was important in the formation of these deposits but that some radiogenic ⁴⁰Ar was derived from crustal rocks. Based on these observations coupled with other geochemical evidence, we suggest that the ore‐forming fluids responsible for the formation of the Ag–Cu–Pb–Zn polymetallic ore deposits in the Baiyangping area of the Lanping basin were mainly derived from crustal fluids. The fluids may have mixed with some amount of air‐saturated water, but there was no significant involvement of mantle‐derived fluids.     

Geochemical Characteristics and Metallogenesis of the Qingkuangshan Ni‐Cu‐PGE Mineralized Mafic‐Ultramafic Intrusion in Huili County,Sichuan Province,SW China

The Qingkuangshan Ni-Cu-PGE deposit, located in the Xiaoguanhe region of Huili County, Sichuan Province, is one of several Ni-Cu-PGE deposits in the Emeishan Large Igneous Province (ELIP). The ore-bearing intrusion is a mafic-ultramafic body. This paper reports major elements, trace elements and platinum-group elements in different types of rocks and sulfide-mineralized samples in the intrusion. These data are used to evaluate the source mantle characteristics, the degree of mantle partial melting, the composition of parental magma and the ore-forming processes. The results show that Qingkuangshan intrusion is part of the ELIP. The rocks have trace element ratios similar to the coeval Emeishan basalts. The primitive mantle-normalized patterns of Ni-Cu-PGE have positive slopes, and the ratios of Pd/Ir are lower than 22. The PGE compositions of sulfide ores and associated rocks are characterized by Ru depletion. The PGE contents in bulk sulfides are slightly depleted relative to Ni and Cu, which is similar to the Yangliuping Ni-Cu-PGE deposit. The composition of the parental magma for the intrusion is estimated to contain about 14.65 wt% MgO, 48.66 wt% SiO2 and 15.48 wt% FeOt, and the degree of mantle partial melting is estimated to be about 20%. In comparison with other typical Ni-Cu-PGE deposits in the ELIP, the Qingkuangshan Ni-Cu-PGE deposit has lower PGE contents than the Jinbaoshan PGE deposit, but has higher PGE contents than the Limahe and Baimazhai Ni-Cu deposit, and has similar PGE contents to the Yangliuping Ni-Cu-PGE deposit. The moderate PGE depletions in the bulk sulfide of the Qingkuanghan deposit suggest that the parental magma of the host intrusion may have undergone minor sulfide segregation at depth. The mixing calculations suggests that an average of 10% crustal contamination in the magma, which may have been the main cause of sulfide saturation in the magma. We propose that sulfide segregation from a moderately PGE depleted magma took place prior to magma emplacement at Qingkuangshan, that small amounts of immiscible sulfide droplets and olivine and chromite crystals were suspended in the ascending magma, and that the suspended materials settled down when the magma passed trough the Qingkuangshan conduit. The Qingkuangshan sulfide-bearing intrusion is interpreted to a feeder of Emeishan flood basalts in the region.     

Geochronology, Geochemistry and Sr-Nd-Pb-Hf Isotopes of No. I Complex from the Shitoukengde Ni–Cu Sulfide Deposit in the Eastern Kunlun Orogen, Western China: Implications for the Magmatic Source, Geodynamic Setting and Genesis

The Shitoukengde Ni-Cu deposit, located in the Eastern Kunlun Orogen, comprises three mafic–ultramafic complexes, with the No. I complex hosting six Ni-Cu orebodies found recently. The deposit is hosted in the small ultramafic bodies intruding Proterozoic metamorphic rocks. Complexes at Shitoukengde contain all kinds of mafic-ultramafic rocks, and olivine websterite and pyroxene peridotite are the most important Ni-Cu-hosted rocks. Zircon U-Pb dating suggests that the Shitoukengde Ni-Cu deposit formed in late Silurian(426–422 Ma), and their zircons have εHf(t) values of-9.4 to 5.9 with the older T_(DM1) ages(0.80–1.42 Ga). Mafic-ultramafic rocks from the No. I complex show the similar rare earth and trace element patterns, which are enriched in light rare earth elements and large ion lithophile elements(e.g., K, Rb, Th) and depleted in heavy rare earth elements and high field strength elements(e.g., Ta, Nb, Zr, Ti). Sulfides from the deposit have the slightly higher δ~(34)S values of 1.9–4.3‰ than the mantle(0 ± 2‰). The major and trace element characteristics, and Sr-Nd-Pb and Hf, S isotopes indicate that their parental magmas originated from a metasomatised, asthenospheric mantle source which had previously been modified by subduction-related fluids, and experienced significant crustal contamination both in the magma chamber and during ascent triggering S oversaturation by addition of S and Si, that resulted in the deposition and enrichment of sulfides. Combined with the tectonic evolution, we suggest that the Shitoukengde Ni-Cu deposit formed in the post-collisional, extensional regime related to the subducted oceanic slab break-off after the Wanbaogou oceanic basalt plateau collaged northward to the Qaidam Block in late Silurian.     

Geochronology and Genesis of the Tiegelongnan Porphyry Cu(Au) Deposit in Tibet: Evidence from U–Pb,Re–Os Dating and Hf,S, and H–O Isotopes

The Tiegelongnan Cu (Au) deposit is the largest copper deposit newly discovered in the Bangong–Nujiang metallogenic belt. The deposit has a clear alteration zoning consisting of, from core to margin, potassic to propylitic, superimposed by phyllic and advanced argillic alteration. The shallow part of the deposit consists of a high sulphidation‐state overprint, mainly comprising disseminated pyrite and Cu–S minerals such as bornite, covellite, digenite, and enargite. At depth porphyry‐type mineralization mainly comprises disseminated chalcopyrite, bornite, pyrite, and a minor vein molybdenite. Mineralization is disseminated and associated with veins contained within the porphyry intrusions and their surrounding rocks. The zircon U–Pb ages of the mineralized diorite porphyry and granodiorite porphyry are 123.1 ± 1.7 Ma (2σ) and 121.5 ± 1.5 Ma (2σ), respectively. The molybdenite Re–Os age is 121.2 ± 1.2 Ma, suggesting that mineralization was closely associated with magmatism. Andesite lava (zircon U–Pb age of 111.7 ± 1.6 Ma, 2σ) overlies the ore‐bodies and is the product of post‐mineralization volcanic activity that played a critical role in preserving the ore‐bodies. Values of ?4.6 ‰ to + 0.8 ‰ δ³⁴S for the metal sulfides (mean ? 1.55 ‰) suggest that S mainly has a deep magmatic source. The H and O isotopic composition is (δD = ?87 ‰ to ?64 ‰; δ¹⁸O_H2O = 5.5 ‰ to 9.0 ‰), indicating that the ore‐forming fluids are mostly magmatic‐hydrothermal, possibly mixed with a small amount of meteoric water. The zircon ε_Hf(t) of the diorite porphyry is 3.7 to 8.3, and the granodiorite porphyry is 1.8 to 7.5. Molybdenite has a high Re from 382.2 × 10^?6 to 1600 × 10^?6. Re and Hf isotope composition show that Tiegelongnan has some mantle source, maybe the juvenile lower crust from crust–mantle mixed source. Metallogenesis of the Tiegelongnan giant porphyry system was associated with intermediate to acidic magma in the Early Cretaceous (~120 Ma). The magma provenance of the Tiegelongnan deposit has some mantle‐derived composition, possibly mixed with the crust‐derived materials.     

Evolution of mineralizing fluids in the Zn–Pb–Cu(–Ag ± Au) skarn and epithermal deposits of the world-class San Martín district, Zacatecas, Mexico

Mineralizing fluids at the San Martín skarn show an evolution characterized by prograde and retrograde associations. The prograde mineral associations consist of (1) a massive garnet zone, (2) a tremolite ± garnet zone, and (3) a late association of quartz, sphalerite, calcite and fluorite lining the vugs in the garnet zone. The fluids of the prograde associations exhibit decreasing temperatures of homogenization (Th) and variable salinities. The fluids of the massive garnet zone have salinities of 36 wt.% NaCl equiv. and Th of 645 to 570 °C, corresponding to pressures of 1055 bar. At the tremolite ± garnet zone, Th range from 438 to 354 °C. In the late association at the endoskarn, the following evolution can be drawn: (a) salinities of 50 to 42 wt.% NaCl equiv., and Th of 455 to 346 °C in quartz, (b) salinities of 46 wt.% NaCl equiv., and Th of 415 to 410 °C in sphalerite, (c) salinities of 50 to 37 wt.% NaCl equiv., and Th of 479 to 310 °C in calcite, (d) salinities of 33 to 28 wt.% NaCl equiv. and of 24 to 22 wt.% KCl in fluorite, and (e) two types of fluids with salinities of 2 and 39 wt.% NaCl equiv. and Th 344 and 300 °C, respectively, in later saccharoidal quartz segregations. The retrograde mineral associations comprise pervasive propylitic alteration to carbonization, and mantos with sulfides. Fluids in epidote have salinities of 7.6 wt.% NaCl equiv. and Th of 287 to 252 °C, and in calcite have salinities of 9.2 to 1 wt.% NaCl equiv. and Th of 188 to 112 °C. Fluids in the sulfide assemblages in the mantos have salinities of 8 to 3 wt.% NaCl equiv. and Th 300 °C, with corresponding pressures of 94 bar. Fluids in late epithermal veins close to the intrusive body have salinities of 10 to 5 wt.% NaCl equiv. and Th of 275 to 200 °C, and distal veins show salinities of 2 to 1 wt.% NaCl equiv. and Th of 160 °C.     

U–Pb and Re–Os Geochronology of Karamay Porphyry Mo–Cu Deposit in Western Junggar,NW China

The Karamay porphyry Mo–Cu deposit, discovered in 2010, is located in the West Junggar region of Xinjiang of northwest China. The deposit is hosted within the Karamay granodiorite porphyry that intruded into Early Carboniferous sedimentary strata and its exo‐contact zone. The LA‐ICPMS U–Pb method was used to date the zircons from the granodiorite samples of the porphyry. Analyses of 12 spots of zircons from the granodiorite samples yield a U–Pb weighted mean age of 300.8 ± 2.1 Ma (2σ). Re–Os dating for five molybdenite samples obtained from two prospecting trenches and three outcrops in the deposit yield a Re–Os isochron age of 294.6 ± 4.6 Ma (2σ), with an initial ¹⁸⁷Os/¹⁸⁸Os of 0.0 ± 1.1. The isochron age is within the error of the Re–Os model ages, demonstrating that the age result is reliable. The Re–Os isochron age of the molybdenite is consistent with the U–Pb age of the granodiorite porphyry, which indicates that the deposit is genetically related with an Early Permian porphyry system. The ages of the Karamay Mo–Cu deposit and the ore‐bearing porphyry are similar to the ages of intermediate‐acid intrusions and Cu–Mo–Au polymetallic deposits in the West Junggar region. This consistency suggests the same geodynamic process to the magmatism and related mineralization.     

Geochemical Constraints on the Origin of Banded Iron Formation‐Hosted Iron Ore from the Archaean Ntem Complex (Congo Craton) in the Meyomessi Area,Southern Cameroon

Banded iron formations (BIFs) are the most significant source of iron in the world. In this study, we report petrographic and geochemical data of the BIF from the Meyomessi area in the Ntem Complex, southern Cameroon, and discuss their genesis and the iron enrichment process. Field investigations and petrography have revealed that the studied BIF samples are hard; compact; weakly weathered; and composed of magnetite, subordinate quartz, and geothite. The geochemical composition of the whole rock reveals that iron and silica represent more than 98 wt% of the average composition, whereas Al₂O₃, TiO₂, and high‐field strength elements (HFSE) contents are very low, similar to detritus‐free marine chemical precipitates. The total iron (TFe) contents range from 48.71 to 65.32 wt % (average of 53.29 wt %) and, together with the low concentrations of deleterious elements (0.19 wt % P on average), are consistent with medium‐grade iron ores by global standards. This interpretation is confirmed by the SiO₂/Fe₂O_3total versus (MgO + CaO + MnO)/Fe₂O_3total discrimination plot in which most of the Meyomessi BIF samples fall in the field of medium‐grade siliceous ore. Only one sample (MGT94) plots in the high‐grade magnetite–geothite ore domain. The high Fe/Ti (376.36), Fe/Al (99.90), and Si/Al (29.26) ratios of the sample are consistent with significant hydrothermal components. The rare earth elements (REE) contents of the studied BIF samples are very low (∑REE: 0.81–1.47 ppm), and the Post‐Archaean Australian Shale (PAAS)‐normalized patterns display weak positive Eu anomalies (Eu/Eu*: 1.15–1.33), suggesting a syngenetic low‐temperature hydrothermal solutions, similar to other BIF worldwide. However, the Meyomessi BIFs show high Fe contents when compared to the other BIFs. This indicates an epigenetic mineralization process affected the Meyomessi BIF. From the above results and based on the field and analytical data, we propose that the genetic model of iron ores at the Meyomessi area involves two stages of the enrichment process, hypogene enrichment of BIF protore by metamorphic and magmatic fluids followed by supergene alteration as indicated by the presence of goethite in the rocks.     

Oxygen and Hydrogen Isotope Stratigraphy of the Rustenburg Layered Suite, Bushveld Complex: Constraints on Crustal Contamination

New ¹⁸O values for plagioclase, pyroxene and olivine, and limitedwhole-rock D values are presented for samples from the RustenburgLayered Suite of the Bushveld Complex, South Africa. In combinationwith existing data, these provide a much more complete compositeO-isotope stratigraphy for the intrusion. Throughout the layeredsuite, mineral ¹⁸O values indicate that the magmas from whichthey crystallized had ¹⁸O values that were about 7·1,that is, 1·4 higher than expected for mantle-derivedmagmas, suggesting extensive crustal contamination. More limitedH-isotope data suggest that the OH present within whole rocks,regardless of the degree of alteration, is of magmatic originand not an alteration phenomenon. There appears to be no systematicchange in ¹⁸O value with stratigraphic height and this requiresthe contamination to have taken place in a ‘staging chamber’before emplacement of the magma(s) into the present chamber.Large amounts (30–40%) of contamination by the lower tomiddle crust are needed to explain these ¹⁸O values, which isin general agreement with previous estimates based on Sr- andNd-isotope data. Alternatively, smaller amounts of contamination(20%) by sedimentary rocks, or their partial melts, representedby the country rock can explain the data, but it is not apparenthow such material could have been present at the depth of the‘staging chamber’ in the lower to middle crust. KEY WORDS: Bushveld Complex; Rustenburg Layered Suite; oxygen isotopes; hydrogen isotopes; crustal contamination     

Facies model of a mixed clastic–carbonate,wave‐dominated open‐coast tidal flat (Tithonian–Berriasian,north‐east Spain)

Detailed logging and analysis of the facies architecture of the upper Tithonian to middle Berriasian Aguilar del Alfambra Formation (Galve sub‐basin, north‐east Spain) have made it possible to characterize a wide variety of clastic, mixed clastic–carbonate and carbonate facies, which were deposited in coastal mudflats to shallow subtidal areas of an open‐coast tidal flat. The sedimentary model proposed improves what is known about mixed coastal systems, both concerning facies and sedimentary processes. This sedimentary system was located in an embayed, non‐protected area of a wide C‐shaped coast that was seasonally dominated by wave storms. Clastic and mixed clastic–carbonate muds accumulated in poorly drained to well‐drained, marine‐influenced coastal mudflat areas, with local fluvial sandstones (tide‐influenced fluvial channels and sheet‐flood deposits) and conglomerate tsunami deposits. Carbonate‐dominated tidal flat areas were the loci of deposition of fenestral‐laminated carbonate muds and grainy (peloidal) sediments with hummocky cross‐stratification. Laterally, the tidal flat was clastic‐dominated and characterized by heterolithic sediments with hummocky cross‐stratification and local tidal sandy bars. Peloidal and heterolithic sediments with hummocky cross‐stratification are the key facies for interpreting the wave (storm) dominance in the tidal flat. Subsidence and high rates of sedimentation controlled the rapid burial of the storm features and thus preserved them from reworking by fair‐weather waves and tides.     

Mineralization events in the Xiaokele porphyry Cu (–Mo) deposit,NE China: Evidence from zircon U–Pb and K‐feldspar Ar–Ar geochronology and petrochemistry

The Great Xing'an Range (GXR), Northeast (NE) China, is a major polymetallic metallogenic belt in the eastern segment of the Central Asian Orogenic Belt. The newly discovered Xiaokele porphyry Cu (–Mo) deposit lies in the northern GXR. Field geological and geochronological studies have revealed two mineralization events in this deposit: early porphyry‐type Cu (–Mo) mineralization, and later vein‐type Cu mineralization. Previous geochronological studies yielded an age of ca. 147 Ma for the early Cu (–Mo) mineralization. Our ⁴⁰Ar/³⁹Ar dating yielded ⁴⁰Ar/³⁹Ar plateau ages of 124.8 ± 0.4 to 124.3 ± 0.4 Ma on K‐feldspar in altered Cu‐mineralized diorite porphyrite dikes that represent the overprinting vein‐type Cu mineralization, consistent with zircon U–Pb ages of the diorite porphyrite (126.4 ± 0.5 to 125.0 ± 0.5 Ma). The Cr and Ni contents and Mg^# of the Xiaokele diorite porphyrites are high. The diorite porphyrites at Xiaokele are enriched in light rare‐earth elements (REEs), and large‐ion lithophile elements (e.g., Rb, Ba, and K), are depleted in heavy REEs and high‐field‐strength elements (e.g., Nb, Ta, and Ti), and have weak negative ε_Hf(t) values (+0.29 to +5.27) with two‐stage model ages (T_DM2) of 1,164–845 Ma. Given the regional tectonic setting in Early Cretaceous, the ore‐bearing diorite porphyrites were likely formed in an extensional environment related to lithospheric delamination and asthenospheric upwelling induced by subduction of the Paleo‐Pacific Plate. These tectonic events caused large‐scale magmatic activity, ore mineralization, and lithospheric thinning in NE China.     

云南二叠纪白马寨铜镍硫化物矿床的成因:地壳混染与矿化的关系

云南金平白马寨-营盘街-带的奥陶纪变砂岩和板岩中出露大量小型约260Ma的镁铁-超镁铁质岩体,其中白马寨地区三个岩体具明显铜-镍硫化物矿化：三号岩体有一个中型铜镍硫化物矿床,一号和二号岩体可见微弱矿化。一号岩体的Ni／Cu值为0．7～2．2,二号岩体的Ni／Cu值为1．4～4．0,与三号岩体的比值（Ni／Cu=-0．5～6．7）相近,说明他们的母岩浆成分接近,为富Mg的镁铁质或苦橄质岩浆。三个岩体遭受不同程度的地壳混染,表现为强烈的Nb（Ta）异常,很低的Nb／La值（O．5～O．7）和很负的￡。。（f）值（一5．1～一9．O）。根据全岩的Th／Yb和Nb／Th值估算,一号岩体的地壳混染程度为5％～20％,二号岩体的地壳混染程度为5％～10％,而三号岩体的地壳混染程度高达35％。三个岩体的地壳混染程度与岩体中硫化物的含量呈正相关关系,表明地壳混染是导致白马寨岩体硫化物饱和的主要因素。     

Two periods of mineralization in Xiaoxinancha Au–Cu deposit,NE China: evidences from the geology and geochronology

The Xiaoxinancha Au–Cu deposit is located at the eastern segment of the Tianshan–Xingmeng orogenic belt in northeast China. The deposit includes porphyry Au–Cu orebodies, veined Au–Cu orebodies and veined Mo mineralizations. All of them occur within the diorite intrusion. The Late Permian diorite, Late Triassic granodiorite, Early Cretaceous granite and granite porphyry are developed in the ore area. The studies on geological features show that the porphyry Au–Cu mineralization is related to the Late Permian diorite intrusion. New geochronologic data for the Xiaoxinancha porphyry Au–Cu deposit yield Permian crystallization zircon U–Pb age of 257 ± 3 Ma for the diorite that hosts the Au–Cu mineralization. Six molybdenite samples from quartz + molybdenite veins imposed on the porphyry Au–Cu orebodies yield an isochron age of 110.3 ± 1.5 Ma. The ages of the molybdenites coeval to zircon ages of the granite within the errors suggest that the Mo mineralization was genetically related to the Early Cretaceous granite intrusion. The formation of the diorite and the related Au–Cu mineralization were caused by the partial melting of the subduction slab during the Late Palaeozoic palaeo‐Asia Ocean tectonic stage. The Re contents and Re–Os isotopic data indicate that the crustal resource is dominated for the Mo mineralization during the Cretaceous extensional setting caused by the roll‐back of the palaeo‐Pacific plate. Copyright © 2014 John Wiley & Sons, Ltd.     

First Reliable Re–Os Ages of Pyrite and Stable Isotope Compositions of Fe(‐Cu) Deposits in the Hami Region,Eastern Tianshan Orogenic Belt,NW China

The Eastern Tianshan Orogenic Belt (ETOB) in NW China is composed of the Dananhu–Tousuquan arc belt, the Kanggurtag belt, the Aqishan–Yamansu belt and the Central Tianshan belt from north to south. These tectonic belts have formed through arc–continent or arc–arc collisions during the Paleozoic. A number of Fe(‐Cu) deposits in the Aqishan–Yamansu belt, including the Heifengshan, Shuangfengshan and Shaquanzi Fe(‐Cu) deposits, are associated with Carboniferous–Early Permian volcanic rocks and are composed of vein‐type magnetite ores. Metallic minerals are dominated by magnetite and pyrite, with minor chalcopyrite. Calcite, chlorite, and epidote are the dominant gangue minerals. Pyrite separates of ores from those three deposits have relatively high and variable Re contents ranging from 3.7 to 184 ppb. All pyrite separates have very low common Os, allowing us calculation of single mineral model ages for each sample. Pyrite separates from the Heifengshan Fe deposit have an ¹⁸⁷Re–¹⁸⁷Os isochron age of 310 ± 23 Ma (MSWD = 0.04) and a weighted mean model age of 302 ± 5 Ma (MSWD = 0.17). Those from the Shuangfengshan Fe deposit have an isochron age of 295 ± 7 Ma (MSWD = 0.28) and a weighted mean model age of 292 ± 5 Ma (MSWD = 0.33). The Shaquanzi Fe‐Cu deposit has pyrite with an isochron age of 295 ± 7 Ma (MSWD = 0.26) and a weighted mean model age of 295 ± 6 Ma (MSWD = 0.23). Pyrite separates from these Fe(‐Cu) deposits have δ³⁴S_CDT ranging from ?0.41‰ to 4.7‰ except for two outliers. Calcite from the Heifengshan Fe deposit and Shaquanzi Fe‐Cu deposit have similar C and O isotope compositions with δ¹³C_PDB and δ¹⁸O_SMOW ranging from ?5.5‰ to ?1.0‰ and from 10‰ to 12.7‰, respectively. These stable isotopic data suggest that S, C, and O are magmatic‐hydrothermal in origin. The association of low‐Ti magnetite and Fe/Cu‐sulfides resembles those of Iron–Oxide–Copper–Gold (IOCG) deposits elsewhere. Our reliable Re–Os ages of pyrite suggest that the Fe(‐Cu) deposits in the Aqishan–Yamansu belt formed at ～296 Ma, probably in a back‐arc extensional environment.     

Geochemical Characterization of Magnetite and Geological Setting of the Iron Oxide ± Iron Silicate ± Iron Carbonate Rich Pb–Zn Sulfides from the La Unión and Mazarrón Stratabound Deposits (SE Spain)

From a mineralogical point of view the La Unión ore field (SE Spain) can be regarded as an oddity as some of its hydrothermal, stratabound type deposits display an extremely unusual paragenesis comprising magnetite ± greenalite ± minnesotaite ± siderite and galena ± sphalerite (IOSC – LZS). Recent mineralogical studies have shown that this paragenesis is also present at the neighboring Mazarrón ore field. These ore fields share a similar geologic setting, involving metamorphic and sedimentary rocks (Paleozoic s.l. to Permian) hosting late Miocene high‐K calc‐alkaline volcanic and subvolcanic rocks. The latter have andesitic to dacitic composition, and triggered hydrothermal activity and ore deposition. This study discusses the detailed mineral chemistry of magnetite samples from Mazarrón and La Unión and provides some hints for the origin of the IOSC – LZS paragenesis. We performed electron microprobe (EPMA) analyses in magnetite samples from La Unión and Mazarrón to determine the contents of minor and trace elements (Zn, Ni, Mn, Cr, V, K, Ca, Ti, Al, Si, Mg). Given that some results fell below the detection limit for the EPMA instrumental conditions we used robust regression on order statistics (robust ROS), with the NADA package in R to deal with these data sets. The Ca + Al + Mn contents in magnetites from San Cristóbal and Emilia are equivalent to the mean contents of those of IOCG, Kiruna, BIF, Cu porphyry, skarn, VMS, hydrothermal and clastic Pb–Zn deposits, but they are low in Ti + V and Ni + Cr. The principal components analysis indicates that Zn, Ni, Cr, V, K, Ca, Ti, and Mg are roughly collinear, therefore correlated, being also independent from Fe. Besides, the function discriminant analysis of data shows that the magnetites from Emilia and San Cristóbal cluster in differentiated groups, thus probably reflecting some differences related to the distance to the magmatic source that triggered the hydrothermal system: proximal in the case of San Cristóbal and distal in Emilia.     

Geological Setting and Origin of Mo–W–Cu Deposits in the Honggor–Shamai District,Inner Mongolia,North China

Twenty‐one Mo–W–Cu deposits and prospects have been discovered in the Honggor–Shamai district, Inner Mongolia, north China during past 5 years. This district is located in the central and western parts of the Chagan Obo–Aoyoute–Chaobulen tectono‐magmatic belt, which is part of the Central Asian Orogenic Belt. The Mo–W–Cu deposits in the district are associated with Mesozoic granitoid intrusions and occur as veins, stockwork, and dissemination. The geological features of these newly discovered deposits are similar to porphyry‐type deposits worldwide. Two mineralization events have been identified: Indosinian (235–224 Ma) and Yanshanian (137–131 Ma). It is proposed that these deposits and prospects in the Honggor–Shamai district were related to the post‐collisional extension linked to the Indosinian orogeny during the Middle–Late Triassic period, but some of those deposits were overprinted by mineralization associated with the Cretaceous magmatic‐hydrothermal (Yanshanian) event.     

Biostratigraphic and isotopic record of the Cenomanian–Turonian deposits in the Ohaba-Ponor section (SW Haţeg, Romania)

The middle Cenomanian–lower Turonian deposits of Ohaba-Ponor section (Southern Carpathians) were studied from biostratigraphic and isotopic points of view. Both the qualitative and semiquantitative nannofloral analyses, as well as the stable isotope (δ¹³C and δ¹⁸O) data support significant palaeoenvironmental changes in the investigated interval. Two δ¹³C positive excursions were recognized: (1) an excursion up to 1.8‰ (PDB) within the middle/late Cenomanian boundary; (2) an excursion up to 2.2‰ (PDB) in the Cenomanian/Turonian boundary interval. The oldest δ¹³C positive excursion recorded (placed within the Acanthoceras jukes-brownei/Eucalycoceras pentagonum Ammonite Zone boundary interval, and in the NC11 Calcareous Nannofossil Zone respectively) could be assigned to the middle Cenomanian Event II (MCEII). During the above-mentioned event, significant increase in abundance of Watznaueria barnesae, followed by successive blooms of Biscutum constans and Eprolithus floralis, were observed. The youngest δ¹³C positive excursion was identified in the Cenomanian/Turonian boundary interval (in the NC12 and lower part of the NC13 Calcareous Nannofossil Zones). Even the amplitude of this δ¹³C positive excursion is lower in the Ohaba-Ponor section, as generally reported, this may represent the regional record of the OAE2. The successive peaks of the nannofossils Biscutum constans, Zeugrhabdotus erectus and Eprolithus floralis indicate episodes of cooler surface water and high fertility, which preceded and lasted the Cenomanian/Turonian boundary event. Additionally, fluctuations of δ¹⁸O values between −2 and −6‰ suggest also cooler conditions within the Cenomanian/Turonian boundary interval.     

Multiple dolomitization events along the Pozalagua Fault (Pozalagua Quarry,Basque–Cantabrian Basin,Northern Spain)

The Pozalagua Quarry in the Basque–Cantabrian Basin of northern Spain exposes a unique set of fault‐associated dolomites that can be studied on a decametre scale. The dolomites developed along the Pozalagua Fault system in slope‐deposited limestones of Albian age. Following marine phreatic diagenesis, the limestones were subject to meteoric karst formation. The resulting cavities were filled either by angular limestone fragments in a black clay‐rich matrix, or by cave floor/pond (now dolomitized) sediments. The subsequent diagenetic history reflects repeated periods of fracturing, fluid expulsion, dissolution and cementation. Contrasting fluid pulses resulted in the formation of a network of hydrothermal karst and the subsequent development of coarse‐crystalline calcite cement, zebra dolomite, recrystallized coarse‐crystalline dolomite, elongated blue–grey coarse‐crystalline dolomite cement in the open fault and, finally, coarse‐crystalline saddle dolomite. Decimetre‐size reworked host‐rock fragments present in the latter two dolomite phases probably reflect roof collapse fragments of a cave system that developed along the Pozalagua Fault system. However, there are also metre‐scale host‐rock fragments that apparently ‘float’ in the coarse‐crystalline saddle dolomites, implying that either fragment assimilation was a widespread process or violent expulsion of fluids occurred along the Pozalagua Fault system. The presence of pre‐dolomite and post‐dolomite stylolites, parallel to bedding, supports a linkage between the diagenetic events and the Late Albian tectonism that affected the region.     

Age and Tectonic Setting of Mesothermal Magmatic Hydrothermal Vein‐Type Pb–Zn–(Ag) Mineralization in the Xiaohongshilazi Deposit,Central Jilin Province,Northeast China

The Xiaohongshilazi deposit located in central Jilin Province, Northeast China, is a newly discovered and medium‐scale Pb–Zn–(Ag) deposit with ore reserves of 34,968 t Pb, 100,150 t Zn, and 158 t Ag. Two‐stage mineralization has been identified in this deposit. Stratiform volcanic‐associated massive sulfide (VMS) Pb–Zn mineralization interbedding with the marine volcanic rocks of the Late Carboniferous–Early Permian Daheshen Formation was controlled by the premineralization E–W‐trending faults. Vein‐type Pb–Zn–(Ag) mineralization occurs within or parallel to the granodiorite and diorite porphyries controlled by the major‐mineralization N–S‐trending faults that cut the stratiform mineralization and volcanic rocks. To constrain the age of vein‐type Pb–Zn–(Ag) mineralization and determine the relationship between mineralization and magmatism, we conducted LA–ICP–MS U–Pb dating on zircon from the ore‐bearing granodiorite and diorite porphyries and Rb–Sr dating on metal sulfide. Granodiorite and diorite porphyries yield zircon U–Pb weighted‐mean ²⁰⁶Pb/²³⁸U ages of 203.6 ± 1.8 Ma (Mean Standard Weighted Deviation [MSWD] = 1.8) and 225.6 ± 5.1 Ma (MSWD = 2.3), respectively. Sulfides from four vein‐type ore samples yield a Rb–Sr isochron age of 195 ± 17 Ma (MSWD = 4.0). These results indicate a temporal relationship between the granodiorite porphyry and vein‐type Pb–Zn–(Ag) mineralization. The granodiorite associated with vein‐type mineralization has high SiO₂ (68.99–70.49 wt.%) and Na₂O (3.9–4.2 wt.%; Na₂O/K₂O = 1.07–1.10) concentrations, and A/CNK values of 0.95–1.04; consequently, the intrusion is classified as a high‐K, calc‐alkaline, metaluminous I‐type granite. The granodiorite porphyry is enriched in large‐ion lithophile elements (e.g. Rb, Th, U, and K) and light REE and is depleted in high‐field‐strength elements (e.g. Nb, Ta, P, and Ti) and heavy REE, indicating that it represents a subduction‐related rock that formed at an active continental margin. Furthermore, the granodiorite porphyry has Mg# values of 31–34, indicating a lower crustal source. Based on petrological and geochemical features, we infer that the ore‐bearing granodiorite porphyry was derived from the partial melting of the lower crust. In summary, mineralization characteristics, cross‐cutting relationships, geochronological data, and regional tectonic evolution indicate that the region was the site of VMS Pb–Zn mineralization that produced stratiform orebodies within the Late Carboniferous–Early Permian marine volcanic rocks of the Daheshen Formation, followed by mesothermal magmatic hydrothermal vein‐type Pb–Zn–(Ag) mineralization associated with granodiorite porphyry induced by the initial subduction of the Paleo‐Pacific Plate beneath the Eurasia Plate during the Late Triassic–Early Jurassic.     

云南金宝山和白马寨铜镍硫化物矿床铂族元素(PGE)地球化学的差异及其成因意义

金宝山和白马寨铜镍硫化物矿床均主要赋存在峨眉山大火山岩省中,但其矿化特征存在许多不同。本文着重对比了金宝山铂钯矿床和白马寨铜镍矿床的铂族元素(PGE)地球化学特征,发现前者表现为高ΣPGE及低的(Cu Ni)、Pd/Ir(3.84~26.49)、Cu/Pd(46.91~1309.58)值和Au/Pd值,相反,后者表现为低ΣPGE、高(Cu Ni)、Pd/Ir(4.72~297.2)、Cu/Pd(10875.13~974788.55)值和较高的Au/Pd值。金宝山和白马寨PGE原始地幔标准化配分模式均主要表现为左倾型,但二者表现为镜像关系。金宝山较白马寨的PGE间相关性好,可能说明白马寨母岩浆经历了较为复杂的地质过程,其铂族元素体系因此受到较大的扰动。结合前人有关杨柳坪铜镍铂族元素矿床的铂族元素数据,认为峨眉地幔柱形成铜镍铂族元素矿床大致可以分成3个阶段:1金宝山阶段:即为S的低度饱和阶段,为峨嵋地幔柱上升初期,吸收少量壳源物质,由于PGE在硫化物中很高的分配系数,导致少量硫化物熔体从硅酸盐中萃取大量PGE和少量Cu-Ni熔离出来,与铬铁矿、橄榄石和辉石等,于高温下结晶分异堆积而成金宝山岩体,形成独立铂钯矿床。...     

Genesis of the Weiquan Ag–Polymetallic Deposit in East Tianshan, China: Evidence from Zircon U–Pb Geochronology and C–H–O–S–Pb Isotope Systematics

The Weiquan Ag-polymetallic deposit is located on the southern margin of the Central Asian Orogenic Belt and in the western segment of the Aqishan-Yamansu arc belt in East Tianshan,northwestern China. Its orebodies, controlled by faults, occur in the lower Carboniferous volcanosedimentary rocks of the Yamansu Formation as irregular veins and lenses. Four stages of mineralization have been recognized on the basis of mineral assemblages, ore fabrics, and crosscutting relationships among the ore veins. Stage I is the skarn stage(garnet + pyroxene), Stage Ⅱ is the retrograde alteration stage(epidote + chlorite + magnetite ± hematite 士 actinolite ± quartz),Stage Ⅲ is the sulfide stage(Ag and Bi minerals + pyrite + chalcopyrite + galena + sphalerite + quartz ± calcite ± tetrahedrite),and Stage IV is the carbonate stage(quartz + calcite ± pyrite). Skarnization,silicification, carbonatization,epidotization,chloritization, sericitization, and actinolitization are the principal types of hydrothermal alteration. LAICP-MS U-Pb dating yielded ages of 326.5±4.5 and 298.5±1.5 Ma for zircons from the tuff and diorite porphyry, respectively. Given that the tuff is wall rock and that the orebodies are cut by a late diorite porphyry dike, the ages of the tuff and the diorite porphyry provide lower and upper time limits on the age of ore formation. The δ~(13)C values of the calcite samples range from-2.5‰ to 2.3‰, the δ~(18)O_(H2 O) and δD_(VSMOW) values of the sulfide stage(Stage Ⅲ) vary from 1.1‰ to 5.2‰ and-111.7‰ to-66.1‰, respectively,and the δ~(13)C, δ~(18)O_(H2 O) and δD_(V-SMOW) values of calcite in one Stage IV sample are 1.5‰,-0.3‰, and-115.6‰, respectively. Carbon, hydrogen, and oxygen isotopic compositions indicate that the ore-forming fluids evolved gradually from magmatic to meteoric sources. The δ~(34)S_(V-CDT) values of the sulfides have a large range from-6.9‰ to 1.4‰, with an average of-2.2‰, indicating a magmatic source, possibly with sedimentary contributions. The ~(206)Pb/~(204)Pb, ~(207)Pb/~(204)Pb, and ~(208)Pb/~(204)Pb ratios of the sulfides are 17.9848-18.2785,15.5188-15.6536, and 37.8125-38.4650, respectively, and one whole-rock sample at Weiquan yields~(206)Pb/~(204)Pb,~(207)Pb/~(204)Pb, and ~(208)Pb/~(204)Pb ratios of 18.2060, 15.5674, and 38.0511,respectively. Lead isotopic systems suggest that the ore-forming materials of the Weiquan deposit were derived from a mixed source involving mantle and crustal components. Based on geological features, zircon U-Pb dating, and C-H-OS-Pb isotopic data, it can be concluded that the Weiquan polymetallic deposit is a skarn type that formed in a tectonic setting spanning a period from subduction to post-collision. The ore materials were sourced from magmatic ore-forming fluids that mixed with components derived from host rocks during their ascent, and a gradual mixing with meteoric water took place in the later stages.