Ore genesis of Badi copper deposit,northwest Yunnan Province,China: evidence from geology,fluid inclusions,and sulfur,hydrogen and oxygen isotopes

The Badi copper deposit is located in Shangjiang town, Shangri-La County, Yunnan Province. Tectonically, it belongs to the Sanjiang Block. Vapor–liquid two-phase fluid inclusions, CO₂-bearing fluid inclusions, and daughter-bearing inclusions were identified in sulfide-rich quartz veins. Microthermometric and Raman spectroscopy studies revealed their types of ore-forming fluids: (1) low-temperature, low-salinity fluid; (2) medium-temperature, low salinity CO₂-bearing; and (3) high-temperature, Fe-rich, high sulfur fugacity. The δ¹⁸O values of chalcopyrite-bearing quartz ranged from 4.96‰ to 5.86‰, with an average of 5.40‰. The δD values of ore-forming fluid in equilibrium with the sulfide-bearing quartz were from ? 87‰ to ? 107‰, with an average of ? 97.86‰. These isotopic features indicate that the ore-forming fluid is a mixing fluid between magmatic fluid and meteoric water. The δ³⁴S values of chalcopyrite ranged from 13.3‰ to 15.5‰, with an average of 14.3‰. Sulfur isotope values suggest that the sulfur in the deposit most likely derived from seawater. Various fluid inclusions coexisted in the samples; similar homogenization temperature to different phases suggests that the Badi fluid inclusions might have been captured under a boiling system. Fluid boiling caused by fault activity could be the main reason for the mineral precipitation in the Badi deposit.     

Magma mixing and gold mineralization in the Maevatanana gold deposit,Madagascar

The Maevatanana gold deposit in Madagascar is hosted by Archean metamorphic rocks in quartz–sulfide veins that are structurally controlled by NNW–SSE trending shear zones. Fluid inclusion data show that the trapping conditions in quartz range from 0.87 to 2.58 kbar at temperatures of 269–362 °C. Laser Raman spectroscopy confirms that these inclusions consist of CO₂, SO₂, and H₂O. The δ³⁴S values of the pyrites range from 1.7‰ to 3.6‰, with an average of 2.25‰, supporting a magmatic origin. Noble gases (He, Ne, Ar, Ke, Xe) are chemically inert, thus will not be involved in chemical reactions during geological processes. Also due to the low concentration of He in the atmosphere and the low solubility of He in aqueous fluids, the atmosphere-derived He is unlikely to significantly affect He abundances and isotopic ratios of crustal fluids, ensures that He production should have the typical crust ³He/⁴He ratios. The ³He/⁴He ratios of fluid inclusions in pyrite from the deposit range from 0.06 to 0.12 Ra, while the ⁴⁰Ar/³⁶Ar ratios range from 6631 to 11441. We infer that the ore-forming fluids could have been exsolved from a granitic magma. The oxygen and hydrogen isotope compositions of the ore-forming fluids (1.5‰ ≤ δ¹⁸O_H2O ≤ 7.8‰; –72‰ ≤ δD ≤ –117‰) indicate they were derived from a granitic magma. Four pyrite samples from the gold deposit yield a precise Re–Os isochron age of 534 ± 13 Ma. Given that the post-collisional granites in northern and central Madagascar were derived by melting of sub-continental lithospheric mantle and formed between 537 and 522 Ma, we can state that the gold metallogenesis was coeval with the crystallization age of these parental magmas. These data could be accounted for the formation of the Maevatanana gold deposit. First, the shear zones hosting the deposit formed around 2.5 Ga, when the Madagascan micro-continental blocks collided with other continental blocks, triggering large-scale tectono-magmatic activity and forming NNW–SSE trending shear zones. The gold mineralization at Maevatanana is coeval with the crystallization age of the Cambrian post-collisional A-type granitoid plutons in northern and central Madagascar, implying that this deposit is associated with extensional collapse of the East African Orogen. This extension in turn induced asthenospheric upwelling, melting of sub-continental lithospheric mantle. These magmas underplated the lower crust, generating voluminous granitic magmas by partial melting of the lower crust. The mixing magma during tectono-thermal reactivation of the East African Orogen produced large volumes of volatiles that extracted gold from the granitic magma and produced Au–S complexes (e.g., Au(HSO₃)²⁻). The shear zones, which were then placed under extensional collapse of the East African Orogen in the Cambrian, formed favorable pathways for the magmatic ore-forming fluids. These fluids then precipitated gold-sulfides that form the Maevatanana gold deposit.     

山东招远金翅岭金矿床H,O,He,Ar同位素组成及其对成矿流体示踪的研究

金翅岭金矿是位于胶东西北部招莱成矿带内的一个中型石英脉型金矿床,受招平断裂带下盘次级NE-NNE向密集构造裂隙带控制,成矿围岩为玲珑花岗岩和郭家岭花岗闪长岩。本文通过对成矿作用过程中的贯通性矿物石英H,O同位素及黄铁矿中流体包裹体He,Ar同位素进行研究,探讨了成矿流体的来源。研究表明:金翅岭金矿床成矿流体的氢、氧同位素组成存在明显的变化趋势,10件样品的氢氧同位素组成δD值变化于-74.80‰～-95.70‰之间,平均值-85.41‰;δ18 O值变化于+1.30‰～+11.12‰之间,平均值为+4.95‰。分析结果显示,成矿流体早期以岩浆水为主,晚期主要为岩浆水和大气降水的混合。黄铁矿流体包裹体3 He/4 He值为0.09R/Ra～1.51R/Ra,平均0.72R/Ra,位于地壳氦和地幔氦之间。根据成矿流体的壳幔二元混合模式进行计算:地幔流体参与成矿的比例为7.49%～11.85%,地壳流体占主导地位。40 Ar/36 Ar值为365.9～4 042.6,集中在地壳流体与地幔流体之间,大气饱和水的范围附近。结合H-O同位素的结果可知,金翅岭金矿床成矿流体是以地壳流体占主导地位的壳幔混合流体,而地壳流体端元又是岩浆水和大气降水的混合流体,并且大气降水参与成矿流体的比例随着成矿作用从早到晚,以及成矿流体由深到浅的运移而不断增多。     

The Daduhe gold field at the eastern margin of the Tibetan Plateau: He, Ar, S, O, and H isotopic data and their metallogenic implications

The Daduhe gold field comprises several shear-zone-controlled Tertiary lode gold deposits distributed at the eastern margin of the Tibetan Plateau. The deposits are hosted in a Precambrian granite–greenstone terrane within the Yangtze Craton. The gold mineralization occurs mainly as auriferous quartz veins with minor sulphide minerals. Fluid inclusions in pyrite have ³He/⁴He ratios of 0.16 to 0.86 R_a, whereas their ⁴⁰Ar/³⁶Ar ratios range from 298 to 3288, indicating a mixing of fluids of mantle and crust origins. The δ³⁴S values of pyrite are of 0.7–4.2‰ (n = 12), suggesting a mantle source or leaching from the mafic country rocks. δ¹⁸O values calculated from hydrothermal quartz are between − 1.5‰ and + 6.0‰ and δD values of the fluids in the fluid inclusions in quartz are − 39‰ and − 108‰. These ranges demonstrate a mixing of magmatic/metamorphic and meteoric fluids. The noble gas isotopic data, along with the stable isotopic data suggest that the ore-forming fluids have a dominantly crustal source with a significant mantle component.     

Stable Isotopic Geochemical and Geochronological Constraints on the Formation of the Shihu Gold Deposit: The Intracontinental Metallogeny of the Taihang Tectonic Belt,Eastern China

The Early Cretaceous Shihu gold deposit is located in the northern segment of the Taihang Tectonic belt, which extends across the central part of the North China Craton. The deposit is hosted predominantly by the Archean metamorphic crystalline units, and is spatially and temporally related to quartz diorite porphyry present extensively throughout the gold deposit. We studied the geology, geochronology and stable isotopic geochemistry. Zircon U–Pb LA–ICP–MS ages of the quartz diorite porphyry at deposit range from 134 ± 1 to 131 ± 2 Ma, which are coeval and probably genetically related to the mineralization. The majority of the sulfides of the gold deposit have δ³⁴S values ranging from ?1 to 2‰, which suggest an homogeneous magmatic source. In addition, the isotopic compositions of δ¹⁸O_fluid and δ¹⁸D_fluid vary from 2.1 to 7.0‰ and ?93 to ?65‰, respectively, suggesting that the magmatic fluids mingled with meteoric water. The Pb isotopic analyses reveal that both the ore‐forming materials and the quartz diorite porphyry originated from the lower crust and may have been mixed with mantle material. The ⁸⁷Sr/⁸⁶Sr_i and ¹⁴³Nd/¹⁴⁴Nd (¹⁴³Nd/¹⁴⁴Nd)_i ratios for the quartz diorite porphyry demonstrate that there was mixing of two end‐member (crust and the mantle) isotopic compositions. These results suggest that the ore‐forming fluids and materials were derived from lower‐crustal melting induced by mantle processes. Processes associated with the formation of the Shihu gold deposit differ significantly from those that characterize orogenic gold deposits, and instead are representative of formation in an intracontinental tectonic environment.     

Genesis of the Au–Bi–Cu–As, Cu–Mo ± W, and base–metal Au–Ag mineralization at the Mountain Freegold (Yukon, Canada): constraints from Ar–Ar and Re–Os geochronology and Pb and stable isotope compositions

The genesis of mineralized systems across the Mountain Freegold area, in the Dawson Range Cu–Au?±?Mo Belt of the Tintina Au province was constrained using Pb and stable isotope compositions and Ar–Ar and Re–Os geochronology. Pb isotope compositions of sulfides span a wide compositional range (²⁰⁶Pb/²⁰⁴Pb, 18.669–19.861; ²⁰⁸Pb/²⁰⁴Pb, 38.400–39.238) that overlaps the compositions of the spatially associated igneous rocks, thus indicating a magmatic origin for Pb and probably the other metals. Sulfur isotopic compositions of sulfide minerals are broadly similar and their δ³⁴S (Vienna-Canyon Diablo Troilite (V-CDT)) values range from ?1.4 to 3.6 ‰ consistent with the magmatic range, with the exception of stibnite from a Au–Sb–quartz vein, which has δ³⁴S values between ?8.1 and ?3.1 ‰. The δ³⁴S values of sulfates coexisting with sulfide are between 11.2 and 14.2 ‰; whereas, those from the weathering zone range from 3.7 to 4.3 ‰, indicating supergene sulfates derived from oxidation of hypogene sulfides. The δ¹³C (Vienna Peedee Belemnite (VPDB)) values of carbonate range from ?4.9 to 1.1 ‰ and are higher than magmatic values. The δ¹⁸O (V-SMOW) values of magmatic quartz phenocrysts and magmatic least-altered rocks vary between 6.2 and 10.1 ‰ and between 5.0 and 10.1 ‰, respectively, whereas altered magmatic rocks and hydrothermal minerals (quartz and magnetite) are relatively ¹⁸O-depleted (4.2 to 7.9 ‰ and ?6.3 to 1.5 ‰, respectively). Hydrogen isotope compositions of both least-altered and altered igneous rock samples are D-depleted (from ?133 to ?161 ‰ Vienna-Standard Mean Ocean Water (V-SMOW)), consistent with differential magma degassing and/or post-crystallization exchange between the rocks and meteoric ground water. Zircon from a chlorite-altered dike has a U–Pb crystallization age of 108.7?±?0.4 Ma; whereas, the same sample yielded a whole-rock Ar–Ar plateau age of 76.25?±?0.53 Ma. Likewise, molybdenite Re–Os model ages range from 75.8 to 78.2 Ma, indicating the mineralizing events are genetically related to Late Cretaceous volcano-plutonic intrusions in the area. The molybdenite Re–Os ages difference between the nearby Nucleus (75.9?±?0.3 to 76.2?±?0.3 Ma) and Revenue (77.9?±?0.3 to 78.2?±?0.3 Ma) mineral occurrences suggests an episodic mineralized system with two pulses of hydrothermal fluids separated by at least 2 Ma. This, in combination with geological features suggest the Nucleus deposit represents the apical and younger portion of the Revenue–Nucleus magmatic-hydrothermal system and may suggest an evolution from the porphyry to the epithermal environments.     

Stable carbon isotopes in selected granitic,mafic, and ultramafic igneous rocks

Noncarbonate (combustion) and carbonate (acid decomposition) carbon were separately analyzed in 18 granitic rocks from a group of related Tertiary intrusions near Crested Butte, Colorado, and 14 mafic and ultramafic rocks from various localities in the western United States. Among the granites, carbonate carbon ranges from nil to 0.76 per cent with δC¹³-values from ?5.6 to ? 9.0‰ (vs PDB); noncarbonate carbon varies from 32–360 ppm with δC¹³-values from ?19.7 to ?26.6‰, The mafic and ultramafic rocks have carbonate carbon contents ranging from 53 ppm to about 2 per cent with δC¹³-values from + 2.9 to ?10.3‰; noncarbonate carbon varies from 26 to 150 ppm with δC¹³-values of ?22.2 to ? 27.l‰ For these samples, carbonate carbon ranges from 12.0 to 29.4‰ heavier than coexisting noncarbonate carbon. This consistent difference between δC¹³ of carbonate and noncarbonate carbon may be an isotopic fractionation effect. Because the specific indigenous form of noncarbonate (combustion) carbon is in doubt, conclusive interpretations regarding isotopic equilibration and fractionation cannot be made.These results have bearing on the assessment of the isotopic composition of mantle carbon and consequently are germane to the question of the origin (source) and history of crustal carbon. If mantle carbon is isotopically similar to noncarbonate (combustion) carbon, i.e. δC¹³-values from ?19.7 to ? 27.1‰, then a simple mantle degassing source for crustal carbon is improbable. Such a result would indicate an additional source of crustal carbon such as from a primitive atmosphere or extra-terrestrial accretion.     

Genesis of the Wulong gold deposit,Liaoning Province,NE China:Constrains from noble gases,radiogenic and stable isotope studies

TheWulong lode deposit contains over 80 tonnes of gold with an average grade of 5.35 g/t.It is one of the largest deposits in Dandong City,Liaoning Province in northeast China.Previous studies on the deposit focused on its geological characteristics,geochemistry,fluid inclusions,and the timing of gold mineralization.However,controversy remains regarding the origin of the ore-forming fluids and metals,and the genesis of the gold deposit.This paper presents zircon UePb and pyrite RbeSr ages and S,Pb,He,and Ar isotopic results along with quartz H and O isotopic data for all litho-units associated with the deposit.Laser ablation inductively coupled mass spectrometry measurements yielded zircon UePb dates for samples of pre-mineralization rocks like granite porphyry dike,the Sanguliu granodiorite,fine-grained diorite,and syn-mineralization diorite,as well as post-mineralization dolerite,and lamprophyre;their emplacement ages are 126
1 Ma,124
1 Ma,123
1 Ma,120
1 Ma,119
2 Ma,and 115
2 Ma,respectively.The pyrite RbeSr isochron age is 119
1 Ma,indicating that both magmatism and mineralization occurred during the Early Cretaceous.The d18OH2O values of ore-forming hydrothermal fluids from the quartzepolymetallic sulfide vein stage vary from 4.8&to 6.5&,and the dDV-SMOW values are between67.7&and75.9&,indicating that the ore-forming fluids were primarily magmatic.The noble gas isotope compositions of fluid inclusions hosted in pyrite suggest that the ore-forming fluids were dominantly derived from crustal sources with minor mantle input.Sulfur isotopic values of pyrite vary between 0.2&and 3.5&,suggesting that S was derived from a homogeneous magmatic source or possibly from fluids derived from the crust.The Pb isotopic compositions of sulfides(207Pb/204Pb?15.51 e15.71,206Pb/204Pb?17.35e18.75,208Pb/204Pb?38.27e40.03)indicate that the Pb of the Wulong gold deposit is a mixture of crust and mantle components.Geochronological and geochemical data,together with the regional geological history,indicate that Early Cretaceous magmatism and mineralization of the Wulong gold deposit occurred during the rollback of the subducting Paleo-Pacific Plate,which resulted in lithospheric thinning and the destruction of the North China Craton(NCC),which indicates that the deposit is of magmaticehydrothermal origin.     

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.     

Origin of the Dachang gold deposit,NW China: constraints from H,O, S,and Pb isotope data

The Dachang gold deposit is located in the Late Triassic Songpan-Ganzi Fold Belt, NE Tibetan Plateau. Gold ore is concentrated as veins along secondary faults and fracture zones in the Bayan Har Group metaturbidites. No exposed felsic plutons are present in the vicinity of the deposit. The auriferous veins contain <15% sulphide minerals, mainly arsenopyrite, pyrite, and stibnite. Gold is commonly enclosed within arsenopyrite and pyrite. Typical alteration around the ore bodies includes silicification, sericitization, and weak carbonatization.

Gold-bearing quartz samples have δ¹⁸O values of 16.9–21.2‰ (V-SMOW) from which δ¹⁸O_H2O values of 6.2–9.6‰ can be calculated from the fluid inclusion temperatures (or 10.0 to 12.7‰ if we used the average arsenopyrite geothermometer temperature of 301°C). The δD values of fluid inclusions in quartz range from –90‰ to –72‰. δ³⁴S values of gold-bearing sulphides mainly range from –5.9‰ to –2.8‰ (V-CDT). Pyrite and arsenopyrite in ores have ²⁰⁶Pb/²⁰⁴Pb ratios of 18.2888 to 18.4702, ²⁰⁷Pb/²⁰⁴Pb ratios of 15.5763 to 15.6712, and ²⁰⁸Pb/²⁰⁴Pb ratios of 38.2298 to 38.8212. These isotopic compositions indicate that the ore-forming fluids were of metamorphic origin, and the S and Pb may have been derived from the host metaturbidites of the Bayan Har Group. The Dachang Au deposit has geological and geochemical features similar to orogenic gold deposits. We propose that the ores formed when the Songpan-Ganzi Fold Belt was intensely deformed by Late Triassic folding and thrusting. Large-scale thrusting resulted in regional allochthons of different scales, followed by secondary faults or fracture zones that controlled the ore bodies.     

Geological,fluid inclusion,and O–C–S–Pb–He–Ar isotopic constraints on the genesis of the Honghuagou lode gold deposit,northern North China Craton

The Honghuagou Au deposit is located in the Chifeng-Chaoyang region within the northern margin of the North China Craton. The auriferous quartz veins are mainly hosted in the mafic gneiss and migmatite of the Neoarchean Xiaotazigou Formation along NNW- and NE-striking faults, with pyrite as the predominant ore mineral. The gold mineralization process can be divided into two stages, involving stage I quartz-pyrite and stage II quartz-calcite-polymetallic sulfide. Three types of fluid inclusions (FIs) have been identified in the Honghuagou deposit, namely, carbonic inclusions, aqueous‑carbonic inclusions, and aqueous inclusions. Quartz of stage I contains all types of FIs, whereas only aqueous inclusions are evident in stage II veins. The FIs of stages I and II yield homogenization temperatures of 275–340 °C and 240–290 °C with salinities of 3.4–10.7 wt% and 1.4–9.7 wt% NaCl eqv., respectively. The ore-forming fluids are characterized by medium temperature and low salinity, belonging to the H₂O–NaCl–CO₂ system. The δ¹⁸O_H2O values of the ore fluids are between 2.1‰ and 5.9‰, within the range of enriched mantle-derived fluids in the North China Craton. The carbon isotope compositions of calcite (δ¹³C_PDB = −4.4‰ to −4‰) are also similar to mantle carbon. He-Ar isotope data (³He/⁴He = 0.38–0.44 Ra; ⁴⁰Ar/³⁶Ar = 330–477) of fluid inclusions in pyrite indicate a mixed crustal and mantle source for the ore-forming fluids. Whereas, S-Pb isotope compositions of sulfides reveal that ore metals are principally derived from crustal rocks. On the basis of available geological and geochemical evidence, we suggest that the Honghuagou deposit is an orogenic gold deposit.     

Genesis of the Maoling gold deposit in the Liaodong Peninsula: Constraints from a combined fluid inclusion,C-H-O-S-Pb-He-Ar isotopic and geochronological studies

The large tonnage Maoling gold deposit (25 t @ 3.2 g/t) is located in the southwest Liaodong Peninsula, North China Craton. The deposit is hosted in the Paleoproterozoic metamorphic rocks. Four stages of mineralization were identified in the deposit: (stage I) quartz-arsenopyrite ± pyrite, (stage II) quartz-gold- arsenopyrite-pyrrhotite, (stage III) quartz-gold- polymetallic sulfide, and (stage IV) quartz-calcite-pyrrhotite. In this paper, we present fluid inclusion, C-H-O-S-Pb-He-Ar isotope data, zircon U-Pb, and gold-bearing sulfide (i.e. arsenopyrite and pyrrhotite) Rb-Sr age of the Maoling gold deposit to constrain its genesis and ore-forming mechanism. Three types of fluid inclusions were distinguished in quartz-bearing veins, including liquid-rich two-phase (WL type), gas-rich two-phase (GL type), and daughter mineral-bearing fluid inclusions (S type). Fluid inclusions data show that the homogenization at temperatures 197 to 372 °C for stage I, 126 to 319 °C for stage II, 119 to 189 °C for stage III, and 115 to 183 °C for stage IV, with corresponding salinities of 3.7 to 22.6 wt.%, 4.7 to 23.2 wt.%, 5.3 to 23.2 wt.%, and 1.7 to 14.9 wt.% NaCl equiv., respectively. Fluid boiling was the critical factor controlling the gold and associated sulfide precipitation at Maoling. Hydrogen and oxygen stable isotopic analyses for quartz yielded δ¹⁸O = ?5.0‰ to 9.8‰ and δ D = ?133.5‰ to ?77.0‰. Carbon stable isotopic analyses for calcite and ankerite yielded δ¹³C = ?2.3‰ to ?1.2‰ and O = 7.9‰ to 14.1‰. The C-H-O isotope data show that the ore-forming fluids were originated from magmatic water with meteoric water input during mineralization. Hydrothermal inclusions in arsenopyrite have ³He/⁴He ratios of 0.002 Ra to 0.054 Ra, and ⁴⁰Ar/³⁶Ar rations of 1225 to 3930, indicating that the ore-forming fluids were dominantly derived from crustal sources almost no mantle input. Sulfur isotopic values of Maoling fine-grained granite range from 6.‰1 to 9.8‰, with a mean of 7.7‰, δ³⁴S values of arsenopyrite from the mineralized phyllite (host rock) range from 8.9‰ to 10.6‰, with a mean of 10.0‰, by contrast, δ³⁴S values of sulfides from ore vary between 4.3‰ and 10.6‰, with a mean of 6.8‰, suggesting that sulfur was mainly originated from both the host rock and magma. Lead radioactive isotopic analyses for sulfides yielded ²⁰⁶Pb/²⁰⁴Pb = 15.830–17.103, ²⁰⁷Pb/²⁰⁴Pb = 13.397–15.548, ²⁰⁸Pb/²⁰⁴Pb = 35.478–36.683, and for Maoling fine-grained granite yielded ²⁰⁶Pb/²⁰⁴Pb = 18.757–19.053, ²⁰⁷Pb/²⁰⁴Pb = 15.596–15.612, and ²⁰⁸Pb/²⁰⁴Pb = 38.184–39.309, also suggesting that the ore-forming materials were mainly originated from the host rocks and magma. Zircon U-Pb dating demonstrates that the Maoling fine-grained granite was emplaced at 192.7 ± 1.8 Ma, and the host rock (mineralized phyllite) was emplaced at some time after 2065.0 ± 27.0 Ma. Arsenopyrite and pyrrhotite give Rb–Sr isochron age of 188.7 ± 4.5 Ma, indicating that both magmatism and mineralization occurred during the Early Jurassic. Geochronological and geochemical data, together with the regional geological history, indicate that Early Jurassic magmatism and mineralization of the Maoling gold deposit occurred during the subducting Paleo-Pacific Plate beneath Eurasia, and the Maoling gold deposit is of the intrusion-related gold deposit type.     

S, C, O, H Isotope Data and Noble Gas Studies of the Maoniuping LREE Deposit, Sichuan Province, China： A Mantle Connection for Mineralization

The Maoniuping REE deposit, located about 22 km to the southwest of Mianning, Sichuan Province, is the second largest light REE deposit in China, subsequent to the Bayan Obo Fe-Nb-REE deposit in the Inner Mongolia Autonomous Region. Tectonically, it is located in the transitional zone between the Panxi rift and the Longmenshan-Jinpingshan orogenic zone. It is a carbonatite vein-type deposit hosted in alkaline complex rocks. The bastnaesite-barite, bastnaesite-calcite, and bastnaesite-microcline lodes are the main three types of REE ore lodes. Among these, the first lode is distributed most extensively and its REE mineralization is the strongest. Theδ34Sv-CDT values of the barites in the ore of the deposit vary in a narrow range of +5.0 to +5.1‰in the bastnaesite-calcite lode and +3.3 to +5.9‰in the bastnaesite-barite lode, showing the isotopic characteristics of magma-derived sulfur. Theδ13Cv-PDB values and theδ518OV-SMOW values in the bastnaesite-calcite lode range from -3.9 to -6.9‰and from +7.3 to +9.7‰, respectively, which fall into the range of "primary carbonatites", showing that carbon and oxygen in the ores of the Maoniuping deposit were derived mainly from a deep source. Theδ13Cv-PDB values of fluid inclusions vary from -3.0 to -5.6‰, with -3.0 to -4.0‰in the bastnaesite-calcite lode and -3.0 to -5.6‰in the bastnaesite-barite lode, which show characteristics of mantle-derived carbon. TheδDv-SMOW values of fluid inclusions range from -57 to -88‰, with -63 to -86‰in the bastnaesite-calcite lode and -57 to -88‰in the bastnaesite-barite lode, which show characteristics of mantle-derived hydrogen. Theδ18OH2OV-SMOW values vary from +7.4 to +8.6‰in the bastnaesite calcite lode, and +6.7 to +7.8‰in the bastnaesite-barite lode, almost overlapping the range of +5.5 to +9.5‰for magmatic water. The 4He content, R/Ra ratios are (13.95 to 119.58×10-6 (cm3/g)STP and 0.02 to 0.11, respectively, and 40Ar/36Ar is 313±1 to 437±2. Considering the 4He increase caused by high contents of radioactive elements, a mantle-derived fluid probably exists in the inclusions in the fluorite, calcite and bastnaesite samples. The Maoniuping deposit and its associated carbonatite-alkaline complex were formed in 40.3 to 12.2 Ma according to K-Ar and U-Pb data. All these data suggest that large quantities of mantle fluids were involved in the metallogenic process of the Maoniuping REE deposit through a fault system.     

Mantle-derived noble gases in ore-forming fluids of the granite-related Yaogangxian tungsten deposit,Southeastern China

More than 90% of the tungsten resources of China are in the Nanling region of South China, and the Yaogangxian vein deposit is the largest tungsten deposit in this region. The tungsten deposits have ages of 150–160 Ma, and are spatially, temporally and genetically related to granites which were previously believed to be produced by crustal anatexis. This paper provides He and Ar isotope data of fluid inclusions in pyrite and arsenopyrite from the Yaogangxian W veins. ³He/⁴He ratios range from 0.41 to 3.03 Ra (where Ra is the ³He/⁴He ratio of air?=?1.39?×?10^?6), and ⁴⁰Ar/³⁶Ar ratios from 328 to 1,191. Moreover, there are excellent correlations between He and Ar isotopic compositions. The results suggest that the ore-forming fluids are a mixture between a crustal fluid containing atmospheric Ar and crustal ⁴He and a fluid containing mantle components. It is likely that the former is a low temperature meteoric fluid, and the later is a fluid exsolved from the W-associated granitic magma, which formed by crustal melting induced by intrusion of a mantle-derived magma.     

A Nd- and O-isotope study of the REE-rich peralkaline Strange Lake granite: implications for Mesoproterozoic A-type magmatism in the Core Zone (NE-Canada)

It is well established that A-type granites enriched in high field strength elements, such as Zr, Nb and the REE, form in anorogenic tectonic settings. The sources of these elements and the processes controlling their unusual enrichment, however, are still debated. They are addressed here using neodymium and oxygen isotope analyses of samples from the 1.24 Ga Strange Lake pluton in the Paleoproterozoic Core Zone of Québec-Labrador, an A-type granitic body characterized by hyper-enrichment in the REE, Zr, and Nb. Age-corrected εNd values for bulk rock samples and sodic amphiboles (mainly arfvedsonite) from the pluton range from ?0.6 to ?5.7, and ?0.3 to ?5.3, respectively. The εNd values for the Napeu Kainiut quartz monzonite, which hosts the pluton, range from ?4.8 to ?8.1. The ¹⁴⁷Sm/¹⁴⁴Nd ratios of the suite and the host quartz monzonite range from 0.0967 to 0.1659, large variations that can be explained by in situ fractionation of early LREE-minerals (Strange Lake), and late hydrothermal HREE remobilization. Oxygen isotope analyses of quartz of both Strange Lake and the host yielded δ¹⁸O values between +8.2 and +9.1, which are considerably higher than the mantle value of 5.7 ± 0.2‰. Bulk rock oxygen isotope analyses of biotite-gneisses in the vicinity of the Strange Lake pluton yielded δ¹⁸O values of 6.3, 8.6 and 9.6‰. The negative εNd values and positive δ¹⁸O values of the Strange Lake and Napeu Kainiut samples indicate that both magmas experienced considerable crustal contamination. The extent of this contamination was estimated, assuming that the contaminants were sedimentary-derived rocks from the underlying Archean Mistinibi (para-) gneiss complex, which is characterized by low εNd and high δ¹⁸O values. Mixing of 5–15% of a gneiss, having an εNd value of ?15 and a δ¹⁸O value of +11, with a moderately enriched mantle source (εNd = +0.9, δ¹⁸O = +6.3) would produce values similar to those obtained for the Strange Lake granites. Based on analogies between the Nain Plutonic Suite and the Gardar alkaline igneous province (SW-Greenland), we conclude that the Strange Lake pluton and associated REE-mineralized anorogenic bodies formed from a combination of subduction-induced fertilization of the sublithospheric mantle, crustal extension and in situ magma evolution.     

Geology and D-O-C Isotope Systematics of the Tieluping Silver Deposit,Henan, China: Implications for Ore Genesis

The Tieluping silver deposit, which is sited along NE-trending faults within the high-grade metamorphic basement of the Xiong‘er terrane, is part of an important Mesozoic orogenic-type Ag-Pb and Au belt recently discovered. Ore formation includes three stages: Early (E), Middle (M) and Late (L), which include quartz-pyrite (E),polymetallic sulfides (M) and carbonates (L), respectively. The E-stage fluids are characterized by δD=-90%c,δ^13CCO2=2.0‰ and δ^18O=9‰ at 373℃, and are deeply sourced; the L-stage fluids, with δD=-70‰, δ^13C CO2=-1.3%c and δ^18O=-2‰, are shallow-sourced meteoric water; whereas the M-stage fluids, with δD=-109‰, δ^13C CO2=0.1%c and δ^18O2‰, are a mix of deep-sourced and shallow-sourced fluids. Comparisons of the D-O-C isotopic systematics of the Estage ore-forming fluids with the fluids derived from Mesozoic granites, Archean-Paleoproterozoic metamorphic basement and Paleo-Mesoproterozoic Xiong‘er Group, show that these units cannot generate fluids with the measured isotopic composition (high δ^180 and δ^13C ratios and low δD ratios) characteristic of the ore-forming fluids. This suggests that the E-stage ore-forming fluids originated from metamorphic devolatilization of a carbonate-shale-chert lithological association, locally rich in organic matter, which could correspond to the Meso-Neoproterozoic Guandaokou and Luanchuan Groups, rather than to geologic units in the Xiong‘er terrane, the lower crust and the mantle. This supports the view that the rocks of the Guandaokou and Luanchuan Groups south of the Machaoying fault might be the favorable sources. A tectonic model that combines collisional orogeny, metallogeny and hydrothermal fluid flow is proposed to explain the formation of the Tieluping silver deposit. During the Mesozoic collision between the South and North China paleocontinents, a crustal slab containing a lithological association consisting of carbonate-shale-chert, locally rich in organic matter (carbonaceous shale) was thrust northwards beneath the Xiong‘er terrane along the Machaoying fault.Metamorphic devolatilization of this underthrust slab provided the ore-forming fluids to develop the Au-Ag-(Pb-Zn) ore belt, which includes the Tieluping silver deposit.     

He–Ar Isotopic Tracing of Pyrite from Ore-forming Fluids of the Sanshandao Au Deposit, Jiaodong Area

The Sanshandao Au deposit is located in the famous Sanshandao metallogenic belt, Jiaodong area. To date, accumulative Au resources of 1000 t have been identified from the belt. Sanshandao is a world-class gold deposit with Au mineralization hosted in Early Cretaceous Guojialing-type granites. Thus, studies on the genesis and ore-forming element sources of the Sanshandao Au deposit are crucial. He and Ar isotopic analyses of fluid inclusions from pyrite(the carrier of Au) indicate that the fluid inclusions have 3 He/4 He=0.043–0.21 Ra with an average of 0.096 Ra and 40 Ar/36 Ar=488–664 with an average of 570.8. These values represent the initial He and Ar isotopic compositions of ore-forming fluids for trapped fluid inclusions. The comparison of H–O isotopic characteristics combined with deposit geology and wall rock alteration reveals that the ore-forming fluids of the Sanshandao Au deposit show mixed crust–mantle origin characteristics, and they mainly comprise crust-derived fluid mixed with minor mantle-derived fluid and meteoric water during the uprising process. The ore-forming elements were generally sourced from pre-Cambrian meta-basement rocks formed by Mesozoic reactivation and mixed with minor shallow crustal and mantle components.     

Carbon and oxygen isotopic compositions of Newania Dolomite Carbonatites, Rajasthan, India: implications for source of carbonatites

The Newania carbonatite complex of Rajasthan, India is one of the few dolomite carbonatites of the world, and oddly, does not contain alkaline silicate rocks thus providing a unique opportunity to study the origin and evolution of a primary carbonatite magma. In an attempt to characterize the mantle source, the source of carbon, and the magmatic and post-magmatic evolution of Newania carbonatites, we have carried out a detailed stable carbon and oxygen isotopic study of the complex. Our results reveal that, in spite of being located in a metamorphic terrain, these rocks remarkably have preserved their magmatic signatures in stable C and O isotopic compositions. The δ¹³C and δ¹⁸O variations in the complex are found to be results of fractional crystallization and low temperature post-magmatic alteration suggesting that like other carbonatites, dolomite carbonatites too fractionate isotopes of both elements in a similar fashion. The major difference is that the fractional crystallization of dolomite carbonatites fractionates oxygen isotopes to a larger extent. The modes of δ¹³C and δ¹⁸O variations in the complex, ?4.5?±?1‰ and 7?±?1‰, respectively, clearly indicate its mantle origin. Application of a multi-component Rayleigh isotopic fractionation model to the correlated δ¹³C versus δ¹⁸O variations in unaltered carbonatites suggests that these rocks have crystallized from a CO₂ + H₂O fluid rich magma, and that the primary magma comes from a mantle source that had isotopic compositions of δ¹³C ~ ?4.6‰ and δ¹⁸O ~ 6.3‰. Such a mantle source appears to be a common peridotite mantle (δ¹³C = ?5.0?±?1‰) whose carbon reservoir has insignificant contribution from recycled crustal carbon. Other Indian carbonatites, except for Amba Dongar and Sung Valley that are genetically linked to Reunion and Kerguelen plumes respectively, also appear to have been derived from similar mantle sources. Through this study we establish that dolomite carbonatites are generated from similar mantle source like other carbonatites, have comparable evolutionary history irrespective of their association with alkaline silicate rocks, and may remain resistant to metamorphism.     

胶东水旺庄金矿床成矿机制:来自S-H-O同位素和流体包裹体的制约

为探讨胶东水旺庄金矿床成因,对载金黄铁矿和石英进行了S-H-O同位素组成及流体包裹体的测试分析,研究表明:黄铁矿δ34S介于7.0‰~8.5‰,流体的δD介于-91.7‰~-82.6‰,δ18O介于2.6‰~5.6‰,发育气-液两相流体包裹体、含CO₂流体包裹体和含子矿物流体包裹体等3类,流体盐度介于1.2%~13.8%（NaCl_eq）,均一温度主要集中于290~350 ℃,成矿期流体为中高温、低盐度的H₂O-CO₂-NaCl±CH₄体系,具有深部岩浆来源特征.流体的不混溶或沸腾作用导致了金的沉淀富集.受中生代太平洋板块俯冲及后撤影响,胶东地区发生了大规模岩浆活动和强烈的地壳隆升,所产生的热隆-伸展构造为该区大规模金矿集中爆发成矿提供了有利条件.在主拆离断层中主要形成破碎带蚀变岩型金矿床,在主拆离断层下盘主要形成石英脉型金矿床.      

Geology,geochemistry, and genesis of Axi: A Paleozoic low-sulfidation type epithermal gold deposit in Xinjiang,China

Axi is a low-sulfidation type epithermal gold deposit hosted in Paleozoic subaerial volcanic rocks in the western Tianshan orogenic belt, Xinjiang, China. The resource is more than 50 t gold at an average grade of > 4.4 ppm. The deposit occurs in the Tulasu volcanic fault-basin in the Paleozoic active continental margin on the northern side of the Yili-Central Tianshan plate. The host rocks are andesitic volcaniclastic rocks of the Paleozoic Dahalajunshan Formation, and the orebodies occur as veins in annular faults of a paleocaldera. Mineralization at Axi can be subdivided into five stages: quartz and/or chalcedony vein, quartz vein, quartz-carbonate vein, sulfide vein and carbonate vein. There are two types of ore host: quartz vein and altered rocks. Ore minerals are native gold, electrum, pyrite, marcasite, arsenopyrite, hematite, limonite, and trace amounts of pyrargyrite, polybasite, naumannite, cerargyrite, sphalerite, chalcopyrite, tetrahedrite, galena, pyrrhotite and clausthalite; gangue minerals are mainly quartz, chalcedony, illite, calcite, siderite, dolomite, adularia and laumontite. The main wall-rock alteration is silicification and phyllic alteration, carbonatization and propylitization. The deposit is characterized by an enrichment, relative to crustal abundance, of Au, Ag, As, Sb, Bi, Hg, Se, Te and Mo, depletion in base metals (Cu, Pb, and Zn), and a low Ag/Au ratio (0.5–3.7).Three types of fluid inclusions were recognized in quartz from the major mineralization stages: liquid aqueous inclusions, liquid-rich two-phase inclusions and small amounts of vapor-rich two-phase inclusions. Microthermometric measurements indicate that the final ice melting temperatures are − 0.3 to − 4.4 °C, corresponding to salinities of 0.5–6.9 wt.% NaCl equiv. (2.2 wt.% NaCl equiv. in average). The peak temperatures of ice melting varies from − 0.4 to − 1.9 °C, corresponding to salinities of 0.7–3.1 wt.% NaCl equiv. Homogenization temperatures range mainly between 120 and 240 °C, with an average of 190 °C and a maximum of 335 °C. The fluid density is 0.73 to 0.95 g/cm³ and thus the estimated maximum mineralization depth is about 700 m.Hydrogen and oxygen isotopic compositions of the ore fluids lie within a narrow range: δD_H2O is − 98 to − 116‰ and δ¹⁸O_H2O − 1.8 to 0.4‰. ³He/⁴He ranges from 0.0218 to 0.138 Ra, with an average of 0.044 Ra, indicating that He derived predominantly from crust with negligible mantle He in the ore fluids. By contrast, the ⁴⁰Ar/³⁶Ar ranges from 317.7 to 866.0, suggesting that crust-derived radioactive ⁴⁰Ar⁎ accounts for 7.0 to 66%, and atmospheric ⁴⁰Ar about 43 to 93% in the ore fluids. Hydrogen, oxygen, carbon, sulfur and noble gas isotopes indicate that the ore-forming fluids of the Axi gold deposit consisted predominantly of circulating meteoric water. Ore-forming metals may have derived mainly from the host volcaniclastic rocks of the Dahalajunshan Formation and basement rocks. The occurrence of adularia, platy calcite, and quartz or sulfide aggregates as pseudomorphs after bladed calcite in ore veins, and occurrence of aqueous liquid, and liquid-rich and vapor-rich two-phase inclusions, indicates that boiling of the ore-forming fluid have occurred, leading to supersaturation of the hydrothermal solution and deposition of ore metals. This is the main mineralization mechanism for quartz-vein type ores in Axi. The ore-forming fluid was buffered to a near-neutral pH in a reduced environment during mineralization. The preservation of this Paleozoic Axi deposit and its discovery required a rapid accumulation of sediments in the basin after formation of the deposit, and minimal amount of erosion after Late Cenozoic uplift.