Modes of occurrence of minerals in the Carboniferous coals from the Wuda Coalfield,northern China: with an emphasis on apatite formation

The mineralogical compositions of the Nos. 9 and 13 coals, which are medium-volatile bituminous coals in rank, from the Wuda Coalfield at the northwestern margin of the Ordos Basin in northern China, were investigated by optical microscopy, field emission-scanning electron microscopy in conjunction with energy-dispersive X-ray spectrometry (SEM-EDX), and X-ray powder diffraction techniques. The minerals in the Wuda coals are mainly represented by quartz, kaolinite, illite, pyrite, marcasite, apatite, dolomite, and ankerite, with trace amounts of anatase, calcite, boehmite, jarosite, gibbsite, anhydrite, and bassanite in some samples. The rod-like pyritized bacteria have been identified with SEM-EDX in Wuda coals. Moreover, the slightly reducing and alkaline environment in the original peat swamp favored bacterial action and propagation. The average concentrations of P₂O₅ in the Nos. 9 and 13 coals are 0.47 and 0.18 %, respectively. Phosphorus is not uniformly distributed within the Wuda coal seam. The maximum content of apatite in Wuda coals in certain horizon can reach up to 91.4 % (on an organic matter-free basis), corresponding to the fluorine and P₂O₅ concentrations of 2803 μg/g and 5.96 %. The high proportion of fluorine and P₂O₅ in the Wuda coals is mainly due to the authigenic apatite. The phosphorus in Wuda coals was probably derived mainly from phospho-proteins in the organic matter of the original peat deposits.     

Geochemical and mineralogical evidence for a coal-hosted uranium deposit in the Yili Basin,Xinjiang, northwestern China

The petrological, geochemical, and mineralogical compositions of the coal-hosted Jurassic uranium ore deposit in the Yili Basin of Xinjiang province, northwestern China, were investigated using optical microscopy and field emission-scanning electron microscopy in conjunction with an energy-dispersive X-ray spectrometer, as well as X-ray powder diffraction, X-ray fluorescence, and inductively coupled plasma mass spectrometry. The Yili coal is of high volatile C/B bituminous rank (0.51–0.59% vitrinite reflectance) and has a medium sulfur content (1.32% on average). Fusinite and semifusinite generally dominate the maceral assemblage, which exhibits forms suggesting fire-driven formation of those macerals together with forms suggesting degradation of wood followed by burning. The Yili coals are characterized by high concentrations of U (up to 7207 μg/g), Se (up to 253 μg/g), Mo (1248 μg/g), and Re (up to 34 μg/g), as well as As (up to 234 μg/g) and Hg (up to 3858 ng/g). Relative to the upper continental crust, the rare earth elements (REEs) in the coals are characterized by heavy or/and medium REE enrichment. The minerals in the Yili coals are mainly quartz, kaolinite, illite and illite/smectite, as well as, to a lesser extent, K-feldspar, chlorite, pyrite, and trace amounts of calcite, dolomite, amphibole, millerite, chalcopyrite, cattierite, siegenite, ferroselite, krutaite, eskebornite, pitchblende, coffinite, silicorhabdophane, and zircon. The enrichment and modes of occurrence of the trace elements, and also of the minerals in the coal, are attributed to derivation from a sediment source region of felsic and intermediate petrological composition, and to two different later-stage solutions (a U–Se–Mo–Re rich infiltrational and a Hg–As-rich exfiltrational volcanogenic solution). The main elements with high enrichment factors, U, Se, As, and Hg, overall exhibit a mixed organic–inorganic affinity. The uranium minerals, pitchblende and coffinite, occur as cavity-fillings in structured inertinite macerals. Selenium, As, and Hg in high-pyrite samples mainly show a sulfide affinity.     

Fluid-induced breakdown of white mica controls nitrogen transfer during fluid–rock interaction in subduction zones

ABSTRACT

In order to determine the effects of fluid–rock interaction on nitrogen elemental and isotopic systematics in high-pressure metamorphic rocks, we investigated three different profiles representing three distinct scenarios of metasomatic overprinting. A profile from the Chinese Tianshan (ultra)high-pressure–low-temperature metamorphic belt represents a prograde, fluid-induced blueschist–eclogite transformation. This profile shows a systematic decrease in N concentrations from the host blueschist (~26 μg/g) via a blueschist–eclogite transition zone (19–23 μg/g) and an eclogitic selvage (12–16 μg/g) towards the former fluid pathway. Eclogites and blueschists show only a small variation in δ¹⁵N_air (+2.1 ± 0.3‰), but the systematic trend with distance is consistent with a batch devolatilization process. A second profile from the Tianshan represents a retrograde eclogite–blueschist transition. It shows increasing, but more scattered, N concentrations from the eclogite towards the blueschist and an unsystematic variation in δ¹⁵N values (δ¹⁵N = + 1.0 to +5.4‰). A third profile from the high-P/T metamorphic basement complex of the Southern Armorican Massif (Vendée, France) comprises a sequence from an eclogite lens via retrogressed eclogite and amphibolite into metasedimentary country rock gneisses. Metasedimentary gneisses have high N contents (14–52 μg/g) and positive δ¹⁵N values (+2.9 to +5.8‰), and N concentrations become lower away from the contact with 11–24 μg/g for the amphibolites, 10–14 μg/g for the retrogressed eclogite, and 2.1–3.6 μg/g for the pristine eclogite, which also has the lightest N isotopic compositions (δ¹⁵N = + 2.1 to +3.6‰).

Overall, geochemical correlations demonstrate that phengitic white mica is the major host of N in metamorphosed mafic rocks. During fluid-induced metamorphic overprint, both abundances and isotopic composition of N are controlled by the stability and presence of white mica. Phengite breakdown in high-P/T metamorphic rocks can liberate significant amounts of N into the fluid. Due to the sensitivity of the N isotope system to a sedimentary signature, it can be used to trace the extent of N transport during metasomatic processes. The Vendée profile demonstrates that this process occurs over several tens of metres and affects both N concentrations and N isotopic compositions.     

A two-stage evolution model for the Amantaytau orogenic-type gold deposit in Uzbekistan

A lithogeochemical, mineral chemical, isotopic, and fluid inclusion study of barren, low-, and high-grade Au-mineralized samples from the shear zone-hosted Amantaytau gold deposit, Uzbekistan, shows that the local host rocks, Late Ordovician–Earlz Silurian carbonacous shales, are likely to have been an important source of Au, As, Ni, and S in the formation of the deposit. Syn-depositional pyrite in these shales contains on average 0.23 ppm Au, 1,083 ppm As, and 861 ppm Ni. The distribution of rare earth elements (REE) indicates a homogeneous source of light REE, whereas the heavy REE distribution reflects most likely primary variations in the sediments. The mineralized zone is marked by a positive Eu anomaly, which supports reducing conditions during the mineralization. A hydrothermal overprint by an aqueous–carbonic fluid is reflected in a high-grade Au-mineralized sample by δ¹³C values of ?13.0?‰ (V-PDB). The δ ³⁴S values in pyrite (?0.13 to +7.30?‰ CDT) from barren and mineralized samples are consistent with marine sulfate being the principal source of the ore sulfur. Assuming a formation temperature of between 300 and 400 °C for the main stage of mineralization, as indicated by the alteration mineral assemblage, the calculated δ ¹⁸O_fluid is between 9.5 and 13.4?‰ V-SMOW, which points at a metamorphic origin of the ore fluid.     

阿尔泰南缘乌拉斯沟铜矿床S-Pb-Sr-Nd-C-H-O同位素特征及其对成矿物质和流体来源限定

新疆乌拉斯沟铜矿床位于阿尔泰造山带南缘克兰盆地内,为近年来新发现的矿床,受NW向断裂控制的脉状矿体产于泥盆系康布铁堡组变质火山岩系中,目前其成矿流体和成矿物质来源尚不明确.在细致的矿床地质研究基础上,通过开展S-Pb-Sr-Nd-C-H-O同位素分析,根据野外和显微镜下观察,可将乌拉斯沟铜矿床的形成划分为黄铁矿-磁铁矿-石英、黄铜矿-绿泥石-绿帘石-石英及石英-碳酸盐阶段.同位素分析结果显示:乌拉斯沟铜矿硫化物样品δ34S值为0.1‰~3.2‰,平均为1.6‰,落入未矿化围岩δ34S值范围（-4.7‰~18.68‰）,矿石硫可能源自康布铁堡组.成矿晚阶段的方解石样品δ13C_V-PDB‰=-1.1‰,δ18O_V-PDB‰=-20.3‰,海相碳酸盐地层和有机碳是可能的碳质来源.8件黄铁矿的Pb同位素为206Pb/204Pb=17.939~18.508（平均18.255）,207Pb/204Pb=15.519~15.674（平均15.578）,208Pb/204Pb=37.881~38.653（平均38.209）,与康布铁堡组围岩类似.初始I_{Sr（220 Ma）}为0.710 4~0.711 7,平均值为0.711 1,初始143Nd/144Nd值为0.512 002~0.512 240（平均0.512 103）.矿石Sr-Nd-Pb同位素组成均指示乌拉斯沟铜矿成矿物质可能主要源自围岩康布铁堡组,并可能有外来成矿物质的加入.流体的δD_V-SMOW变化于-103.8‰~-92‰（平均值为-99.2‰）,石英和方解石矿物的δ18O_V-SMOW值集中在9.4‰~11.5‰（平均值为10.4‰）,δ18O_H2O值为2.1‰~4.2‰（平均值为3.1‰）,结合流体包裹体物理化学特征,成矿热液可能来源于变质水,但可能受到大气降水的影响而偏移.因此,乌拉斯沟铜矿成矿物质主要来源于赋矿围岩的变质脱挥发分作用,这与造山型矿床的成矿机制吻合.      

Geological and isotopic evidence for magmatic-hydrothermal origin of the Ag–Pb–Zn deposits in the Lengshuikeng District,east-central China

The Lengshuikeng ore district in east-central China has an ore reserve of ～43 Mt with an average grade of 204.53 g/t Ag and 4.63 % Pb?+?Zn. Based on contrasting geological characteristics, the mineralization in the Lengshuikeng ore district can be divided into porphyry-hosted and stratabound types. The porphyry-hosted mineralization is distributed in and around the Lengshuikeng granite porphyry and shows a distinct alteration zoning including minor chloritization and sericitization in the proximal zone; sericitization, silicification, and carbonatization in the peripheral zone; and sericitization and carbonatization in the distal zone. The stratabound mineralization occurs in volcano-sedimentary rocks at ～100–400 m depth without obvious zoning of alterations and ore minerals. Porphyry-hosted and stratabound mineralization are both characterized by early-stage pyrite–chalcopyrite–sphalerite, middle-stage acanthite–native silver–galena–sphalerite, and late-stage pyrite–quartz–calcite. The δ³⁴S values of pyrite, sphalerite, and galena in the ores range from ?3.8 to +6.9‰ with an average of +2.0‰. The C–O isotope values of siderite, calcite, and dolomite range from ?7.2 to ?1.5‰ with an average of ?4.4‰ (V-PDB) and from +10.9 to +19.5‰ with an average of +14.8‰ (V-SMOW), respectively. Hydrogen, oxygen, and carbon isotopes indicate that the hydrothermal fluids were derived mainly from meteoric water, with addition of minor amounts of magmatic water. Geochronology employing LA–ICP–MS analyses of zircons from a quartz syenite porphyry yielded a weighted mean ²⁰⁶Pb/²³⁸U age of 136.3?±?0.8 Ma considered as the emplacement age of the porphyry. Rb–Sr dating of sphalerite from the main ore stage yielded an age of 126.9?±?7.1 Ma, marking the time of mineralization. The Lengshuikeng mineralization classifies as an epithermal Ag–Pb–Zn deposit.     

Sulfur geochemistry of Jurassic high-sulfur coals from Egypt

Jurassic high-sulfur coals from the Maghara area in Egypt were analyzed for the abundance and isotopic composition of different forms of sulfur. Analyses indicated that the sulfur occurs in the form of organic, pyrite, and sulfate forms. Pyrite sulfur represents the major fraction, while sulfate sulfur is minor and could be formed during sample preparation for the analyses.The δ³⁴S CDT values of the organic sulfur are positive ranging between 1.0‰ and 13.5‰ with an average of 9.1‰. Pyrite δ³⁴S values are also positive ranging between 1.5‰ and 15.4‰ with an average of 6.6‰. The high δ³⁴S values of the organic sulfur in the Maghara coals suggest a freshwater origin of the organic components of these coals. The lack of correlation between pyrite and organic sulfur isotopes implies different incorporation mechanisms of sulfur. The high-sulfur contents along with the positive and high δ³⁴S values suggest a marine origin of pyrite sulfur and support the geological interpretation of marine invasion after the peat formation that was responsible for the incorporation of the pyrite sulfur.The occurrence of pyrite as euhedral crystals as well as the high and positive δ³⁴S values of the pyrite sulfur indicates the formation of pyrite during diagenesis as a result of marine water invasion of the preexisting peat in a brackish coastal plain environment.     

Impact of river damming on sediment texture and trace metals distribution along the watershed and the coastal zone of Nestos River (NE Greece)

This study examines the sediment particle size distribution and the trace metal concentrations from a dammed-river watershed (Nestos River) to its deltaic zone in NE Greece. The study area is relatively unpolluted. The distribution of trace metals (Cu, Cr, Cd, Ni, Pb, Hg) in sediments throughout the catchment area showed selective “trapping” of certain elements behind the two artificial dams (Thissavros and Platanovrisi dams) in the watershed and a sudden reduction downstream (83% for Cd, 81% for Cr, 94% for Cu, 90% for Ni, 86% for Hg and 33% for Pb). Marked sediment particle separation is observed at the upstream dam (Thissavros), where coarse material including sand is trapped (coarse fraction 12.9–49.3%). Fine-grained material (<63 μm) is trapped behind the Platanovrisi dam (68.1%), and the reservoir showed elevated metal concentrations, especially for Cu and Cd (16.3 and 0.5 μg/g, respectively). Lead exhibited a homogenous distribution throughout the watershed (20.1–32.3 μg/g). All other trace metals (Cu, Cr, Cd, Ni and Hg) decline sharply downstream of the dam complex. In the delta system, nearshore sediments consist of shallow deposits in the vicinity of river mouth and are enriched in Cr (4.4–53.0 μg/g) and Ni (2.6–44.3 μg/g), while the further offshore and slightly deeper (20–40 m) sediments illustrate elevated Hg (0–0.07 μg/g), Cd (0.09–0.18 μg/g), Cu (11.5–18.3 μg/g) and Ni (38–54.5 μg/g).     

Stable isotopes and noble gases in the Xishimen gold deposit,central North China Craton: metallogeny associated with lithospheric thinning and crust–mantle interaction

Quartz-vein type gold mineralization at Xishimen is a recently discovered gold deposit in the central North China Craton. More than 50 auriferous quartz veins occur in this region within a NNW–SSE-trending fault zone 4600 m in length and 3–10 m wide. Wall rocks are mainly Precambrian tonalite–trondhjemite–granodiorite (TTG) gneisses and associated supracrustals, modified by K-feldspathization and pyrite-phyllic hydrothermal alteration. Based on detailed field and petrographic studies, we identify five episodes of mineralization: pyrite-phyllic stage (I), coarse-grained pyrite-milky white quartz stage (II), fine-grained smoky grey quartz-pyrite stage (III), fine-grained smoky grey quartz-polymetallic sulphide stage (IV), and quartz-carbonate stage (V). We present results of δ³⁴S analysis of sulphide minerals from the different stages which show tightly clustered values in the range of –1.0‰ to 2.1‰, close to those of mantle and meteorite sulphur. Lead isotopic ratios of pyrite from the early to main stages also show restricted ranges with ²⁰⁶Pb/²⁰⁴Pb of 16.289–17.286, ²⁰⁷Pb/²⁰⁴Pb of 15.217–15.453, ²⁰⁸Pb/²⁰⁴Pb of 37.012–38.232, implying lower crustal input. ³He/⁴He and ⁴⁰Ar/³⁶Ar ratios of fluid trapped in pyrite are 0.68 Ra to 1.20 Ra (where Ra is the ³He/⁴He ratio of air = 1.4 × 10^?6) and 540.9–1065, respectively. ³He and ⁴Ar concentrations vary from 10.05 to 18.5 (10^?7 cm³STP/g) and 6.15 to 17.4 (10^?7cm³STP/g), respectively, with calculated mantle helium ranging from 8.47% to 14.96% (average 11.01%). δ¹⁸O_Q and δ¹⁸D_Q values of quartz range from 8.0‰ to 13.2‰ and –101.9‰ to –70.5‰, respectively, with calculated δ¹⁸O_W values of the mineralizing fluid ranging from 1.11‰ to 5.72‰, suggesting the mixing of magmatic aqueous fluid with meteoric water during gold precipitation. We correlate the mixed crust–mantle signature of the ore-forming sources to magmatism and metallogeny associated with Mesozoic inhomogeneous lithosphere thinning in the central North China Craton.     

Sulphur‐isotope study of the massive sulphide orebody at Woodlawn,New South Wales

³⁴S/³²S ratios have been measured in a suite of samples from the stratabound, volcanogenic massive sulphide deposit at Woodlawn, N.S.W. ³⁴S values for the sulphides vary as follows: in the ore horizon, pyrite +6.7 to +9.2%. (mean +8.1‰), sphalerite +5.2 to +8.6‰. (mean +6.9‰), chalcopyrite +6.4 to +7.0‰ (mean +6.7‰) and galena +2.8 to +5.5‰ (mean +4.4‰); in the vein mineralization, the host volcanics—pyrite +8.7 to +11.4%. (mean +9.8‰), sphalerite +7.8 to + 10.3‰ (mean +9.2‰), chalcopyrite; +8.8 to +10.1‰ (mean +9.2‰) and galena +6.9 to +7.2‰ (mean +7.1‰). Barite from the upper ore horizon levels has an isotopic composition of +30.0‰, consistent with its having originated from Silurian ocean sulphate. The general order of ³⁴S enrichment in the sulphides is pyrite > chalcopyrite ～ sphalerite > galena. Isotopic fractionations in the systems galena/sphalerite/pyrite and chalcopyrite/pyrite indicate an equilibration temperature of 275–300°C. This temperature is considered to represent that of sulphide deposition.     

Acid-sulphate Type Alteration and Mineralization in the Desmos Caldera, Manus Back-arc Basin, Papua New Guinea

Abstract: The Onsen acid‐sulphate type of mineralization is located in the Desmos caldera, Manus back‐arc basin. Hydrothermal precipitates, fresh and altered basaltic andesite collected from the Desmos caldera were studied to determine mineralization and mobility of elements under seawater dominated condition of hydrothermal alteration. The mineralization is characterized by three stages of advanced argillic alteration. Alteration stage I is characterized by coarse subhedral pyrophyllite with disseminated anhedral pyrite and enargite which were formed in the temperature range of 260–340°C. Alteration stage II which overprinted alteration stage I was formed in the temperature range of 270–310°C and is characterized by euhedral pyrite, quartz, natroalunite, cristobalite and mixed layer minerals of smectite and mica with 14–15 Å XRD peak. Alteration stage III is characterized by amorphous silica, native sulphur, covellite, marcasite and euhedral pyrite, which has overprinted alteration stages I and II. Relative to the fresh basaltic andesite samples, the rims and cores of the partly altered basaltic andesite samples have very low major, minor and rare earth elements content except for SiO₂ which is much higher (58–78 wt%) than SiO₂ content of the fresh basaltic andesite (55 wt%). REE patterns of the partly altered basaltic andesite specimens are variably depleted in LREE and have pronounced negative Eu anomalies. Normalization of major, minor and REE content of the partly altered basaltic andesites to the fresh basaltic andesite indicates that all the elements except for SiO2 in the partly altered basaltic andesite are strongly lost (e.g. Al₂O₃ = ‐8.3 to ‐10.9 g/100cm³, Ba = ‐2.2 to ‐5.6 mg/100cm³, La = ‐130 to ‐200 μg/100cm³) during the alteration process. Abnormal depletion of MgO, total Fe as Fe₂O₃, LREE especially Eu and enrichment of SiO₂ in the altered basaltic andesites from the Desmos caldera seafloor is caused by interaction of hot acidic hydrothermal fluid, which originates from a mixing of magmatic fluid and seawater.     

Sulphur- and lead-isotope geochemistry of the Arapuçandere lead–zinc–copper deposit,Biga Peninsula,northwest Turkey

The Arapuçandere Pb–Zn–Cu ore body is a typical vein-type lead–zinc deposit of the Biga Peninsula, and is currently being mined for lead and zinc. In the study area, Permian–Triassic metamorphic rocks, Triassic metaclastic and metabasic rocks, Oligocene–Miocene granitoids, Miocene volcanic rocks, and Quaternary terrigenous sediments crop out. The ore deposits developed as Pb–Zn–Cu-bearing veins along faults in Triassic metasandstone and metadiabase. Microscopic studies reveal that the veins contain galena, sphalerite, chalcopyrite, pyrite, marcasite, covellite, and specular hematite as ore minerals, and quartz, calcite, and barite as gangue minerals. Analysed sulphur-isotope compositions (δ³⁴S_VCDT) of galena, sphalerite, and chalcopyrite range from ? 5.9 to ? 1.9‰ (average ? 3.4‰), from ? 5.5 to ? 1.7‰ (average ? 4.2 ‰), and from ? 3.5 to ? 0.9‰ (average ? 2.6‰), respectively; that of H₂S in the hydrothermal fluid was in the calculated range of ? 5.8 to +0.1‰ (average ? 2.5‰). These isotopic values suggest that magmatic sulphur dominates in sulphides, mixed with minor, isotopically light sulphur. Because no contemporaneous magmatic activity is associated with mineralization, it may be assumed that sulphur was leached from the surrounding Triassic units, mainly from metabasic, partly from metaclastic rocks. Lead-isotope studies indicate a model age of 114–63 Ma for the lead reservoir, in accord with possible sulphur-bearing local source rocks. Thus, the sulphur and lead deposited in the studied ore veins were probably leached from Triassic metabasic and metaclastic rocks some time during the Early Cretaceous to the Palaeocene.     

煤中黄铁矿的铼-锇同位素含量及其地质意义

采用Carius管溶样方法,通过热电离质谱对淮北煤田煤中黄铁矿样品的Re、Os含量及其同位素进行了测定,得出黄铁矿样品中Re和Os含量分别为1·22~1·29ng/g和0·0046~0·0054ng/g。对两个样品同位素定年测定得出,其年龄值分别为(73·9±3·2)Ma和(33±9)Ma,两个样品的年龄相差约258~286Ma。含量和同位素年龄差值表明两个样品是不同时代形成的黄铁矿。Re-Os同位素体系比值揭示黄铁矿所赋存的地质体受到来自地壳物质的显著混染。另外,γOTs参数也证实了这一点。该参数分别为+17和+18,表明了有富含Re母体的地壳物质的加入,这为煤中Re-Os含量及地质理论研究提供了参考资料。     

Geology,mineralogy, and sulfur isotope geochemistry of the Sargaz Cu–Zn volcanogenic massive sulfide deposit,Sanandaj–Sirjan Zone,Iran

The Sargaz Cu–Zn massive sulfide deposit is situated in the southeastern part of Kerman Province, in the southern Sanandaj–Sirjan Zone of Iran. The stratigraphic footwall of the Sargaz deposit is Upper Triassic to Lower Jurassic (?) pillowed basalt, whereas the stratigraphic hanging wall is andesite. Mafic volcanic rocks are overlain by andesitic volcaniclastics and volcanic breccias and locally by heterogeneous debris flows. Rhyodacitic flows and volcaniclastics overlie the sequence of basaltic and andesitic rocks. Based on the bimodal nature of volcanism, the regional geologic setting and petrochemistry of the volcanic rocks, we suggest massive sulfide mineralization in the Sargaz formed in a nascent ensialic back-arc basin. The current reserves (after ancient mining) of the Sargaz deposit are 3 Mt at 1.34% Cu, 0.38% Zn, 0.08%Pb, 0.24 g/t Au, and 7 g/t Ag. The structurally dismembered massive sulfide lens is zoned from a pyrite-rich base, to a pyrite?±?chalcopyrite-rich central part, and a sphalerite–chalcopyrite-rich upper part, with a sphalerite-rich zone lateral to the upper part. The main sulfide mineral is pyrite, with lesser chalcopyrite and sphalerite. The feeder zone, comprised of a vein stockwork consists of quartz–sulfide–sericite pesudobreccia and, in the deepest part, chlorite–quartz–pyrite pesudobreccia. Footwall hydrothermal alteration extends at least 70–80 m below the massive sulfide lens and more than a hundred meters along strike from the massive sulfide lens. Jasper and Fe–Mn bearing chert horizons lateral to the sulfide deposit represent low-temperature hydrothermal precipitates of the evolving hydrothermal system. Based on mineral textures and paragenetic relationships, the growth history of the Sargaz deposit is complex and includes: (1) early precipitation of sulfides (protore) on the seafloor as precipitation of fine-grained anhedral pyrite, sphalerite, quartz, and barite; (2) anhydrite precipitation in open spaces and mineral interstices within the sulfide mound followed by its subsequent dissolution, formation of breccia textures, and mound clasts and precipitation of coarse-grained pyrite, sphalerite, tetrahedrite–tennantite, galena and barite; (3) replacement of pre-existing sulfides by chalcopyrite precipitated at higher temperatures (zone refining); (4) continued “refining” led to the dissolution of stage 3 chalcopyrite and formation of a base-metal-depleted pyrite body in the lowermost part of the massive sulfide lens; (5) carbonate veins were emplaced into the sulfide lens, replacing stage 2 barite. The δ³⁴S composition of the sulfides ranges from +2.8‰ to +8.5‰ (average, +5.6‰) with a general increase of δ³⁴S ratios with depth within the massive sulfide lens and underlying stockwork zone. The heavier values indicate that some of the sulfur was derived from seawater sulfate that was ultimately thermochemically reduced in deep hydrothermal reaction zones.     

Recycling of palaeo-Pacific subducted oceanic crust related to a Fe–Cu–Au mineralization in the Xu-Huai region of North Anhui-Jiangsu,East China: Geochronological and geochemical constraints

ABSTRACT

In this study, Early Cretaceous skarn deposits and genesis of their host diorite/monzodiorite porphyry in the Xuzhou-Huaibei (Xu-Huai) region, northern Anhui-Jiangsu have been discussed by detailed geochemical work. In-situ zircon U–Pb dating of the diorites related to Fe–Cu–Au deposits shows that they were formed between 131.4 ± 1.5 Ma and 130.8 ± 1.8 Ma. Geochemical data indicate a depletion of high field strength elements (HFSE) in the diorite porphyry with similarity to that of arc-related igneous rocks. The diorite porphyry was probably derived from typical arc magmas related to continental margin subduction characterized by light rare earth elements (LREEs) enrichment and HFSE depletion. REEs compositions of apatite in the diorite porphyry indicate that the dioritic magma was produced from the metasomatized subcontinental mantle by slab-derived fluids. The magma was proven to be a high oxygen fugacity; thus, it was particularly conducive to the precipitation of Fe, Cu, Au and other ore-forming elements. The δ³⁴S values of pyrite and chalcopyrite of Fe–Cu–Au ores range from ?0.2‰ to 2.8‰, indicating that the sulphur in the ore was probably derived from deep-seated magmas. Integrated with geochronological and geochemical analyses, we suggest that the Early Cretaceous igneous suites associated with Fe–Cu–Au deposits in the Xu-Huai region are related to recycling subduction of Pacific oceanic crust.     

Formation process of pyrite polyframboid based on the heavy-metal analysis by micro-PIXE

Pyrite framboid in sedimentary rocks could be concerned with arsenic contamination in groundwater of acidic environment and has been studied for the formation process of its unique morphology. However, not much has been discussed about the formation process based on the heavy-metal distribution in pyrite framboids and their aggregates. To reveal the formation process of pyrite framboids and their aggregates, mudstone from the Late Cretaceous Hakobuchi Group, central Hokkaido, Japan, are investigated for mode, petrographical, mineralogical, and micro-PIXE (particle-induced X-ray emission) analysis in this study. Spherical and sub-spherical pyrite framboids observed in polyframboids can be divided into two types based on the diameter of framboids (D) and the average diameter of microcrystals (d) within framboids: type 1, ranging from 2 to 9 μm and from 0.4 to 0.9 μm, respectively, and type 2, ranging from 8 to 50 μm and from 0.5 to 1.8 μm, respectively. Based on the quantitative traverse analyses and 2-D elemental mapping results by micro-PIXE, heterogeneities in the concentrations of heavy metals within the analyzed aggregations of pyrite are exhibited. On the basis of the As and Pb zoning patterns, the time range and chronological stages of pyrite-aggregation growth are revealed.     

Multiple isotope composition (S, Pb, H, O, He, and Ar) and genetic implications for gold deposits in the Jiapigou gold belt, Northeast China

The Jiapigou gold belt (>150 t Au), one of the most important gold-producing districts in China, is located at the northeastern margin of the North China Craton. It is composed of 17 gold deposits with an average grade around 10 g/t Au. The deposits are hosted in Archean gneiss and TTG rocks, and are all in shear zones or fractures of varying orientations and magnitudes. The δ³⁴S values of sulfide from ores are mainly between 2.7?‰ and 10?‰. The Pb isotope characteristics of ore sulfides are different from those of the Archean metamorphic rocks and Mesozoic granites and dikes, and indicate that they have different lead sources. The sulfur and lead isotope compositions imply that the ore-forming materials might originate from multiple, mainly deep sources. Fluid inclusions in pyrite have ³He/⁴He ratios of 0.6 to 2.5 Ra, whereas their ⁴⁰Ar/³⁶Ar ratios range from 1,444 to 9,805, indicating a dominantly mantle fluid with a negligible crustal component. δ¹⁸O values calculated from hydrothermal quartz are between ?0.2?‰ and +5.9?‰, and δD values of the fluids in the fluid inclusions in quartz are from ?70?‰ to ?96?‰. These ranges suggest dominantly magmatic water with a minor meteoric component. The noble gas isotopic data, along with the stable isotopic data, suggest that the ore-forming fluids have a dominantly mantle source with minor crustal addition.     

Petrogenesis and tectonic implications of the middle Silurian volcanic rocks in northern West Junggar,NW China

Zircon U–Pb geochronological and geochemical analyses are reported for a suite of the middle Silurian volcanic rocks from northern West Junggar (NW China), southern Central Asian Orogenic Belt (CAOB), with the aim to investigate the sources, petrogenesis, and tectonic implications. Laser ablation inductively coupled plasma mass spectrometry (LA-ICP-MS) U–Pb analysis from an andesite yielded a concordant weighted mean ²⁰⁶Pb/²³⁸U age of 429 ± 3 Ma, indicating the presence of middle Silurian volcanic rocks in northern West Junggar. The andesite is tholeiite series and characterized by minor variations in compositions (SiO₂ = 55.68–59.17 wt.%, Al₂O₃ = 14.56–17.7 wt.%, TiO₂ = 0.55–1.23 wt.%, Na₂O + K₂O = 3.46–7.16 wt.%, and P₂O₅ = 0.15–0.37 wt.%), with wider MgO content (2.18–6.48 wt.%) and Mg# (57.4–77.9). All andesitic rocks are enriched in large-ion lithophile elements (LILEs; e.g. Rb, Ba, K, and Th) and light rare earth elements (LREEs), but strongly depleted in some high field strength elements (HFSEs; e.g. Nb, Ta and Ti), with slight negative Eu anomalies (Eu/Eu* = 0.8–1). These features suggest that the andesitic magmas were derived from 2–8% partial melting of a garnet lherzolite depleted mantle source with subducted sediments metasomatized by slab-derived fluids. Combining the current study with those data in existing literature, we conclude that the middle Silurian volcanic rocks formed in an intra-oceanic subduction setting during consumption of the Irtysh–Zaysan Ocean, and further confirm the eastern extension of the early Palaeozoic Boshchekul–Chingiz volcanic arc of East Kazakhstan in China.     

Geochemical and mineralogical anomalies of the late Permian coal in the Zhijin coalfield of southwest China and their volcanic origin

This paper describes the influence of volcanic ash on the concentrations and occurrences of associated elements in coal in the Zhijin Coalfield in western Guizhou Province, China. Our studies reveal that the No. 9 coal seam in the Zhijin Coalfield has very high content of Fe (4.34%), Cu (369.90 μg/g), U (49.6 μg/g), Mo (63.10 μg/g), Zn (33.97 μg/g), and Zr (841.80 μg/g). The studies have also found that elements, such as Fe and Cu, do not occur as sulfides in this coal seam, in sharp contrast to many other coal seams in China. The geochemical and mineralogical anomalies of the coal seam are attributed to synsedimentary volcanic ash. In addition to normal macerals and minerals in coal, a volcanic-influenced material (VIM) derived from volcanic ash, detrital material of terrigenous origin and organic matter was identified under polarized-light reflectance microscopy and scanning electron microscopy equipped with energy-dispersive X-ray (EDX) analyzer. The volcanic-influenced material is the main carrier of the above elements in this coal. Six types of the volcanic-influenced material (VIM-1, VIM-2, VIM-3, VIM-4, VIM-5, and VIM-6) are further distinguished on the basis of their structures and compositions. To the best of our knowledge, this is the first report that presents a detailed classification of coal components with a high content of volcanic ash.     

Rare Earth Element Geochemistry of Late Palaeozoic Coals in North China

Instrumental Neutron Activation Analysis (INAA) was done to determine the abundances of rare earth elements (REE) of 58 samples of Late Palaeozoic Carboniferous-Permian coals and related rocks in North China. Detailed study of REE geochemistry shows that the ∑REE of most coals studied in this paper is in a normal range between 30×10-6 and 80×10-6 with a mean of 56×10-6. The REE in the Taiyuan Formation in the northern part of North China are much richer than those in the southern part. This is due to the shorter distance to the source area in the north. Moreover, the IREE is in positive correlation to coal ash, especially closely related to the content of clay minerals <2μm in size. This reveals that most REE were carried by terrigenous clastic materials, especially fine clay minerals. In the coals the light REE (LREE) are much richer than the heavy REE (HREE), and the LREE/HREE ratio in coals generally varies from 2 to 8. The LREE/HREE ratio of high-ash, low-sulphur coals is higher than that of lo