Geology,geochemistry and fluid inclusions of the Bianjiadayuan Pb–Zn–Ag deposit,Inner Mongolia,NE China: Implications for tectonic setting and metallogeny

The Bianjiadayuan Pb–Zn–Ag deposit in the Southern Great Xing'an Range consists of quartz-sulfide vein-type and breccia-type mineralization related to granite. Vein orebodies are localized in NW-trending extensional faults. Hydrothermal alteration is well developed and includes silicification, potassic alteration, chloritization and sericitization. Three stages of mineralization are recognized based on field evidence and petrographic observation and are marked by assemblages of quartz–arsenopyrite–pyrite (stage I), quartz–pyrrhotite–chalcopyrite–sphalerite (stage II) and quartz–galena–silver minerals (stage III). The granite, with a zircon age of 143.2 ± 1.5 Ma (n = 14, MSWD = 0.93), is subalkaline, peraluminous and is classified as A2-type granite originating in a post-orogenic extensional setting during the opening of suture zone between the North China Craton and the Siberia Craton from the Late Jurassic to the Early Cretaceous. The δ³⁴S_CDT values of sulfides, ranging from 3.19 to 10.65‰, are not consistent with the majority of magmatic hydrothermal deposits in the SGXR, possibly implying accessory source in addition to magmatic source. Microthermometric measurements show that ore minerals were deposited at intermediate temperatures (347.8–136.4 °C) with moderate salinities (2.9–14.4 wt.% NaCl). Ore-forming fluids were derived largely from magmatic hydrothermal processes, with the addition of meteoric water in late stage. Successive precipitation of Pb, Zn and Ag occurred with changes of physicochemical conditions. Overall considering mineralization features, ore-forming fluids and materials and tectonic setting and comparing with adjacent deposits, the Bianjiadayuan deposit is a mesothermal magmatic hydrothermal vein-type Pb–Zn–Ag deposit controlled by fractures and related to A2-type granite in response to the tectonic/magmatic/hydrothermal activity in late Jurassic. Besides, the explosive breccias in the west area require more attention in future exploration.     

Fluid source and physicochemical conditions of the polymetallic mineralization in Gawuch Formation,Kohistan Island Arc,NW Pakistan

The Cu-Sb-Pb polymetallic vein deposit is hosted by metavolcanics rocks of the Gawuch Formation at the Kaldom Gol area of the northwest Kohistan arc terrain in northern Pakistan. The mineralization is closely associated with the dioritic to granodioritic rocks of the Lowari pluton, which was intruded into the Gawuch metavolcanics. Details of ore characterization and processes of ore genesis of this evidently hydrothermal mineralization are not well documented. Integrating petrographic, mineral-chemical and isotopic investigations, this study aims to comprehend the source of hydrothermal fluids, geochemical evolution, mineral inclusions and physicochemical conditions of the Cu-Sb-Pb polymetallic vein deposit in Gawuch metavolcanics in the Kohistan arc terrain in northern Pakistan. The mineralization is distinguished into three types of ore-gangue associations: Type Ia, Type Ib, and Type II. The textural study revealed two pyrite generations: (i) Py1 displaying euhedral to subhedral habits and containing scarce inclusions, and (ii) Py2 occurring as anhedral grains hosting abundant inclusions. Type Ia is characterized by Py1 associated with abundant quartz (Qz) showing comb texture, sericite (Ser), and minor chlorite (Chl). Type Ib comprises Qz + Ser + Chl and Py2, chalcopyrite (Ccp), and magnetite (Mag). Type II is represented by mosaic quartz, rhombic adularia, and bladed calcite, and the ore minerals fahlore and galena. Alteration zones composed of Qz-Ser ± Chl and Qz-Ser-Chl, surround Type I (a, b) and Type II veins, respectively. Fahlore and galena mostly replace pyrite of Type Ia and chalcopyrite of Type Ib. In addition, malachite, azurite, hematite and covellite occur as secondary (supergene) minerals. The Co/Ni ratios (>1) of Kaldom Gol pyrites suggest that the ore-forming fluids were hydrothermal in origin and Py1 and Py2 solidified at 221–304 °C and 225–261 °C, respectively. The LA-ICP-MS time-resolved depth profiles confirm the existence of sphalerite, and chalcopyrite inclusions in pyrite (Py1 and Py2) and millerite, bravoite, vaesite, Au-tellurides, native Au and galena inclusions in chalcopyrite and fahlore. Sulfur isotope compositions of pyrites (δ³⁴S = Py1, −0.58 to +2 ‰; δ³⁴S = Py2, −0.24 to +2.04 ‰) indicate that the ore-forming fluids were derived from magmatic source (s). The mineral assemblage, hydrothermal alterations, textures, temperature and δ³⁴S of pyrites suggest that the Cu-Sb-Pb polymetallic mineralization at Kaldom Gol represents an intermediate-sulfidation type of epithermal deposit.     

Metallogenesis and hydrothermal evolution of the Tonggou Cu deposit in the Eastern Tianshan: Evidence from fluid inclusions,H-O-S isotopes,and Re-Os geochronology

The Tonggou Cu polymetallic deposit in the Bogda Orogenic Belt, Eastern Tianshan shows evidence for three stages of hydrothermal mineralization: early pyrite veins (Stage 1), polymetallic sulfide ± epidote–quartz (Stage 2), and late-stage pyrite–calcite veins (Stage 3). Fluid inclusion petrography and microthermometry analyses indicate that the liquid-rich aqueous inclusions (L), vapour-rich aqueous inclusions (V), and NaCl daughter mineral–bearing three phase inclusions (S) formed during the main stage of mineralization, and that the ore fluids represent high-temperature and high-salinity H₂O-NaCl hydrothermal fluids that underwent boiling. Stable isotope (H, O) data indicate that the ore fluids of the Tonggou deposit were originally derived from magmatic water in Stage 2 and subsequently mixed with local meteoric water during Stage 3. Sulphur isotope compositions (6.7‰ to 10.9‰) are consistent with the δ³⁴S values of pyrite from the Qijiaojing Formation sandstone, indicating the primary source of the sulphur ore. Furthermore, chalcopyrite grains separated from the chalcopyrite-rich ore samples yield an isochron age of 303 ± 12 Ma (MSWD = 1.2). These results indicate that the Tonggou deposit is a transition between high–sulfidation and porphyry deposits which formed in the Late Carboniferous. It also suggests an increased likelihood for the occurrence of Cu (Au, Mo) in the Bogda Orogenic Belt, especially at locations where the Cu-Zn deposits are thicker; further deep drilling and exploration are encouraged in these areas.     

Pyrite textures and compositions from the Zhuangzi Au deposit,southeastern North China Craton: implication for ore-forming processes

The Zhuangzi Au deposit in the world-class Jiaodong gold province hosts visible natural gold, and pyrite as the main ore mineral, making it an excellent subject for deciphering the complex hydrothermal processes and mechanisms of gold precipitation. Three types of zoned pyrite crystals were distinguished based on textural and geochemical results from EPMA, SIMS sulfur isotopic analyses and NanoSIMS mapping. Py0 has irregular shapes and abundant silicate inclusions and was contemporaneous with the earliest pyrite–sericite–quartz alteration. It has low concentrations of As (0–0.3 wt.%), Au and Cu. Py1 precipitated with stage I mineralization shows oscillatory zoning with the bright bands having high As (0.4–3.9 wt.%), Au and Cu contents, whereas the dark bands have low contents of As (0–0.4 wt.%), Au and Cu. The oscillatory zoning represents pressure fluctuations and repeated local fluid phase separation around the pyrite crystal. The concentration of invisible gold in Py1 is directly proportional to the arsenic concentration. Py1 is partially replaced by Py2 which occurs with arsenopyrite, chalcopyrite and native gold in stage II. The replacement was likely the result of pseudomorphic dissolution–reprecipitation triggered by a new pulse of Au-rich hydrothermal fluids. The δ³⁴S values for the three types of pyrite are broadly similar ranging from +?7.1 to +?8.8‰, suggesting a common sulfur source. Fluid inclusion microthermometry suggests that extensive phase separation was responsible for the gold deposition during stage II mineralization. Uranium–Pb dating of monazite constrains the age of mineralization to ca. 119 Ma coincident with a short compressional event around 120 Ma linked to an abrupt change in the drift direction of the subducting Pacific plate.     

江西武山铜矿床海底喷流与岩浆热液叠加成矿作用: 控矿地质条件、矿石结构构造与矿床地球化学制约

长江中下游成矿带存在一套产于泥盆系五通组砂岩和石炭系黄龙组白云质灰岩层间的层状含铜硫化物矿体,对其成因存在很大争议。本文以产出典型层状矿体的武山铜矿为解剖重点,结合区域控矿地质要素、矿石结构构造特征及矿石中黄铁矿的稀土元素地球化学,提出层状矿体是海底喷流同生沉积与岩浆热液叠加成矿作用的产物。对武山铜矿层状矿体中的胶黄铁矿和黄铁矿、矽卡岩矿体中黄铁矿和脉状矿体中黄铁矿进行的稀土元素含量分析发现,从层状矿体胶黄铁矿、层状矿体黄铁矿、到矽卡岩和脉状矿体黄铁矿,稀土总量和稀土配分曲线显示递变规律,即层状矿体胶黄铁矿具有较低的稀土总量和轻重稀土分异不明显的较平坦型配分曲线;而矽卡岩和脉状矿体黄铁矿具有较高的稀土总量和轻重稀土分异较明显的右倾型配分曲线。层状矿体黄铁矿的稀土特征则介于两者之间,反映了岩浆热液的叠加作用。根据矿物组合共生关系及矿石结构构造的研究,可将武山铜矿黄铁矿分为3个期次:I期为微球粒、草莓状、条带状、纹层状沉积型黄铁矿; II期为半自形、自形粒状和港湾状黄铁矿,可见与长英质斑晶、岩屑或晶屑凝灰岩伴生或共生, 说明黄铁矿形成与同沉积期火山凝灰岩的密切关系。III期为块状、粗晶状、碎裂状黄铁矿。黄铜矿的形成晚于I、II期黄铁矿,成微粒状、脉状交错穿插或包裹早期球粒状、粒状黄铁矿及长英质矿物。对新发现的灰泥丘构造的详细研究表明,武山铜矿中含矿的灰泥丘与武山外围乌石街出露的不含矿的灰泥丘具有不同的特征,其中前者具有封闭的孔洞系统,而后者为开放的孔洞系统。总之,武山铜矿控矿地质条件、矿石结构构造及不同类型矿石黄铁矿的稀土元素证据表明矿床存在两期成矿事件,即海西期海底喷流同生沉积成矿期和燕山期岩浆热液叠加成矿期。     

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.     

大兴安岭北段岔路口斑岩Mo-热液脉状Zn-Pb成矿系统硫化物微量元素的分布、起源及其勘探指示

岔路口斑岩Mo-Zn-Pb矿床位于大兴安岭北段,是近年来新发现的超大型斑岩-热液脉状Mo-Zn-Pb成矿系统,脉状Zn-Pb矿化直接叠置在斑岩Mo矿化顶部。本文挑选岔路口斑岩型矿化及热液脉型矿化的黄铁矿、闪锌矿、方铅矿,通过EMPA、ICP-MS等多种方法分析硫化物的主微量元素组成,发现岔路口各阶段硫化物均富集Mo元素,相比于斑岩型矿化各阶段中的黄铁矿,Zn、Pb、Mn、Cd、Ga、Ag、Bi等元素在铅锌矿阶段内相对富集;相比于过渡阶段,铅锌阶段闪锌矿中Mo、Co元素及方铅矿中的Bi、Cd和Ag元素含量下降。微量元素在不同阶段内的变化可能是流体降温和天水混合的结果。黄铁矿的稀土总量与成矿岩体最接近,且与成矿岩体和围岩有相似的稀土配分模式,并有较明显的Eu负异常;黄铁矿宽广的Y/Ho比值(25.0~39.0)与成矿岩体的Y/Ho比值范围(27.4~38.7)最接近,同时包括了围岩相对较窄的Y/Ho比值(25.7~31.3),这表明成矿物质主要与成矿岩体同源,可能加入了一定量的围岩物质,岔路口硫化物富Mo的特征受控于深部斑岩Mo矿化岩浆-热液系统。对比东秦岭-大别W-Mo-Pb-Zn矿集区的远源热液脉状Pb-Zn矿床,岔路口浅部近源脉状矿化中的黄铁矿具有更高含量Mo/Ag-Bi/Sb比值和Mo/Pb-Sn/Sb比值,因此浅部硫化物的高Mo含量以及黄铁矿中相关元素比值的高值,可为脉状Zn-Pb矿化附近隐伏斑岩钼矿化的勘探提供新线索。此外,与其他热液脉状和斑岩型矿床相比,岔路口矿床硫化物更富集中高温元素;且综合分析多类矿床的硫化物的微量元素后,本文还初步查明不同矿床类型硫化物富集的微量元素,这一尝试可为矿床成因的判断提供新的思路。     

Porphyry-Style Petropavlovskoe Gold Deposit,the Polar Urals: Geological Position,Mineralogy, and Formation Conditions

Geological and structural conditions of localization, hydrothermal metasomatic alteration, and mineralization of the Petropavlovskoe gold deposit (Novogodnenskoe ore field) situated in the northern part of the Lesser Ural volcanic–plutonic belt, which is a constituent of the Middle Paleozoic island-arc system of the Polar Urals, are discussed. The porphyritic diorite bodies pertaining to the late phase of the intrusive Sob Complex play an ore-controlling role. The large-volume orebodies are related to the upper parts of these intrusions. Two types of stringer–disseminated ores have been revealed: (1) predominant gold-sulfide and (2) superimposed low-sulfide–gold–quartz ore markedly enriched in Au. Taken together, they make up complicated flattened isometric orebodies transitory to linear stockworks. The gold potential of the deposit is controlled by pyrite–(chlorite)–albite metasomatic rock of the main productive stage, which mainly develops in a volcanic–sedimentary sequence especially close to the contacts with porphyritic diorite. The relationships between intrusive and subvolcanic bodies and dating of individual zircon crystals corroborate a multistage evolution of the ore field, which predetermines its complex hydrothermal history. Magmatic activity of mature island-arc plagiogranite of the Sob Complex and monzonite of the Kongor Complex initiated development of skarn and beresite alterations accompanied by crystallization of hydrothermal sulfides. In the Early Devonian, due to emplacement of the Sob Complex at a depth of approximately 2 km, skarn magnetite ore with subordinate sulfides was formed. At the onset of the Middle Devonian, the large-volume gold porphyry Au–Ag–Te–W ± Mo,Cu stockworks related to quartz diorite porphyry—the final phase of the Sob Complex— were formed. In the Late Devonian, a part of sulfide mineralization was redistributed with the formation of linear low-sulfide quartz vein zones. Isotopic geochemical study has shown that the ore is deposited from reduced, substantially magmatic fluid, which is characterized by close to mantle values δ³⁴S = 0 ± 1‰, δ¹³C =–6 to–7‰, and δ¹⁸O = +5‰ as the temperature decreases from 420–300°C (gold–sulfide ore) to 250–130°C (gold–(sulfide)–quartz ore) and pressure decreases from 0.8 to 0.3 kbar. According to the data of microanalysis (EPMA and LA-ICP-MS), the main trace elements in pyrite of gold orebodies are represented by Co (up to 2.52 wt %), As (up to 0.70 wt %), and Ni (up to 0.38 wt %); Te, Se, Ag, Au, Bi, Sb, and Sn also occur. Pyrite of the early assemblages is characterized by high Co, Te, Au, and Bi contents, whereas the late pyrite is distinguished by elevated concentrations of As (up to 0.7 wt %), Ni (up to 0.38 wt %), Se (223 ppm), Ag (up to 111 ppm), and Sn (4.4 ppm). The minimal Au content in pyrite of the late quartz–carbonate assemblage is up to 1.7 ppm and geometric average is 0.3 ppm. The significant correlation between Au and As (furthermore, negative–0.6) in pyrite from ore of the Petropavlovskoe deposit is recorded only for the gold–sulfide assemblage, whereas it is not established for other assemblages. Pyrite with higher As concentration (up to 0.7 wt %) is distinguished only for the Au–Te mineral assemblage. Taking into account structural–morphological and mineralogical–geochemical features, the ore–magmatic system of the Petropavlovskoe deposit is referred to as gold porphyry style. Among the main criteria of such typification are the spatial association of orebodies with bodies of subvolcanic porphyry-like intrusive phases at the roof of large multiphase pluton; the stockwork-like morphology of gold orebodies; 3D character of ore–alteration zoning and distribution of ore components; geochemical association of gold with Ag, W, Mo, Cu, As, Te, and Bi; and predominant finely dispersed submicroscopic gold in ore.     

滇东南都龙超大型锡锌多金属矿床黄铁矿LA-ICPMS微量元素组成研究

滇东南马关都龙是一个以锡锌为主,共-伴生铟、铜、铅、钨、铁、银等多种元素的锡锌多金属超大型矿床。虽然前人从矿物学、矿床地球化学、年代学等不同角度开展了较多的研究,该矿床锡锌多金属矿化为燕山晚期岩浆热液活动的产物已是不争的事实,但关于该矿床是否存在热水沉积作用及其与锡锌多金属成矿作用的关系依然存在较大争议。本文选取都龙矿区广泛存在的黄铁矿作为主要研究对象,在矿相学基础上利用LA-ICPMS对不同阶段黄铁矿的微量元素组成开展了系统的研究。野外及显微鉴定结果表明,矿区存在四种类型(期次)的黄铁矿,即:鲕状黄铁矿Py1;穿切或交代Py1的细脉状黄铁矿Py2;与闪锌矿等硫化物共生的自形黄铁矿Py3;包裹早期黄铁矿或闪锌矿等硫化物的他形黄铁矿Py4。LA-ICPMS分析结果表明,该矿床黄铁矿中富集多种微量元素,其中Co、Ni、As、Ge等元素以类质同象的形式存在黄铁矿晶格中,而其余元素多以显微矿物包体形式赋存于黄铁矿中。上述四期黄铁矿微量元素组成存在较大差别,Py1相对富集Zn和As,而其余微量元素含量较低,Co与Ni含量较低,Co/Ni比值远低于1.00,其微量元素组成与典型沉积作用形成黄铁矿基本一致; Py2与Py1具有相似的微量元素组成特征,其Co/Ni比值接近Py1变化范围; Py3和Py4除富集Zn、As外,Mn、Co、Ni、Cu、Sb、Pb、Bi元素含量也相对较高,其Co/Ni比值相对较高,多大于1,与典型岩浆热液型黄铁矿微量元素组成相似,而与沉积型黄铁矿差异明显。结合各阶段黄铁矿产出地质特征,对比不同类型黄铁矿微量元素组成,本研究认为:Py1鲕状黄铁矿为热水沉积作用形成; Py2为Py1变质改造形成的细脉状黄铁矿,其微量元素继承了Py1; Py3为岩浆热液活动形成的自形黄铁矿; Py4为岩浆热液活动晚期形成的他形黄铁矿,Ag和Bi组成作为区分不同成因类型黄铁矿的化学指标的潜力。矿区早期沉积作用形成鲕状黄铁矿过程可能为后期成矿作用提供了部分硫源及少量Zn等成矿物质,海西-印支期区域变质改造作用对矿区成矿作用影响不大,而燕山晚期岩浆热液活动才是矿区锡多金属大规模成矿作用的主导因素。     

Geology,Fluid Inclusion,and Sulfur Isotope Studies of the Chehugou Porphyry Molybdenum–Copper Deposit,Xilamulun Metallogenic Belt,NE China

The Chehugou Mo–Cu deposit, located 56 km west of Chifeng, NE China, is hosted by Triassic granite porphyry. Molybdenite–chalcopyrite mineralization of the deposit mainly occurs as veinlets in stockwork ore and dissemination in breccia ore, and two ore‐bearing quartz veins crop out to the south of the granite porphyry stock. Based on crosscutting relationships and mineral paragenesis, three hydrothermal stages are identified: (i) quartz–pyrite–molybdenite ± chalcopyrite stage; (ii) pyrite–quartz ± sphalerite stage; and (iii) quartz–calcite ± pyrite ± fluorite stage. Three types of fluid inclusions in the stockwork and breccia ore are recognized: LV, two‐phase aqueous inclusions (liquid‐rich); LVS, three‐phase liquid, vapor, and salt daughter crystal inclusions; and VL, two‐phase aqueous inclusions (gas‐rich). LV and LVS fluid inclusions are recognized in vein ore. Microthermometric investigation of the three types of fluid inclusions in hydrothermal quartz from the stockwork, breccia, and vein ores shows salinities from 1.57 to 66.75 wt% NaCl equivalents, with homogenization temperatures varying from 114°C to 550°C. The temperature changed from 282–550°C, 220–318°C to 114–243°C from the first stage to the third stage. The homogenization temperatures and salinity of the LV, LVS and VL inclusions are 114–442°C and 1.57–14.25 wt% NaCl equivalent, 301–550°C and 31.01–66.75 wt% NaCl equivalent, 286–420°C and 4.65–11.1 wt% NaCl equivalent, respectively. The VL inclusions coexist with the LV and LVS, which homogenize at the similar temperature. The above evidence shows that fluid‐boiling occurred in the ore‐forming stage. δ³⁴S values of sulfide from three type ores change from ?0.61‰ to 0.86‰. These δ³⁴S values of sulfide are similar to δ³⁴S values of typical magmatic sulfide sulfur (c. 0‰), suggesting that ore‐forming materials are magmatic in origin.     

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.     

Tracking magmatic and hydrothermal Nb–Ta–W–Sn fractionation using mineral textures and composition: A case study from the late Cretaceous Jiepailing ore district in the Nanling Range in South China

The Jiepailing mining district in the Nanling range in South China is well-known for its granite-related Sn–Be–F-mineralization. Recently, drill holes have exposed an Nb–Ta–W–Sn mineralized granitic porphyry and topaz-bearing granite–greisen at depth, which we have studied here, using mineral (columbite, rutile, wolframite, cassiterite, zircon, and mica) major- and trace-element compositional data, mineral textures, and zircon and columbite U–Pb geochronology. Our age data shows that the porphyry and the granite and their mineralization formed at ~ 91–89 ± 1 Ma in the late-Cretaceous, and thus subsequent to the main ore-forming events of the region. Continuous mineral compositional trends indicate that the studied granitoids are related by progressive fractionation. We propose that: (1) subhedral–euhedral, low-Ta columbite crystallized from melt; (2) euhedral–subhedral rutile and wolframite and subhedral and subhedral cassiterite up to ~ 30 μm in size formed at the magmatic–hydrothermal transition of the system; and (3) high-Ta columbite and subhedral cassiterite up to ~ 10 μm in size formed from subsolidus hydrothermal fluids. In combination with the Nb, Ta, W, and Sn compositions of zircon and mica, their textures and compositional variation allow us to track the magmatic to hydrothermal rare-metal fractionation (concentration, mobilization, and deposition) of the system in detail, despite our limited access to it through only two exploration drill cores. Using the Nb, Ta, W, and Sn concentrations in zircon (refractory, early-crystallized) and in micas (late equilibrated), respectively, was particularly useful for tracing the partial loss of Sn and W ore components from the intrusion, and to constrain the information which is crucial for any rigorous ore exploration.     

Cu–Mo Differential Mineralization Mechanism of the Dabate Polymetallic Deposit in Western Tianshan,NW China: Evidence from Geology,Fluid Inclusions,and Oxygen Isotope Systematics

Classic porphyry Cu–Mo deposits are mostly characterized by close temporal and spatial relationships between Cu and Mo mineralization. The northern Dabate Cu–Mo deposit is a newly discovered porphyry Cu–Mo polymetallic deposit in western Tianshan, northwest China. The Cu mineralization postdates the Mo mineralization and is located in shallower levels in the deposit, which is different from most classic porphyry Cu–Mo deposits. Detailed field investigations, together with microthermometry, laser Raman spectroscopy, and O‐isotope studies of fluid inclusions, were conducted to investigate the origin and evolution of ore‐forming fluids from the main Mo to main Cu stage of mineralization in the deposit. The results show that the ore‐forming fluids of the main Mo stage belonged to an NaCl + H₂O system of medium to high temperatures (280–310°C) and low salinities (2–4 wt% NaCl equivalent (eq.)), whereas that of the main Cu stage belonged to an F‐rich NaCl + CO₂ + H₂O system of medium to high temperatures (230–260°C) and medium to low salinities (4–10 wt% NaCl eq.). The δ¹⁸O values of the ore‐forming fluids decrease from 3.7–7.8‰ in the main Mo stage to ?7.5 to ?2.9‰ in the main Cu stage. These data indicate that the separation of Cu and Mo was closely related to a large‐scale vapor–brine separation of the early ore‐forming fluids, which produced the Mo‐bearing and Cu‐bearing fluids. Subsequently, the relatively reducing (CH₄‐rich) Mo‐bearing, ore‐forming fluids, dominantly of magmatic origin, caused mineralization in the rhyolite porphyry due to fluid boiling, whereas the relatively oxidizing (CO₂‐rich) Cu‐bearing, ore‐forming fluids mixed with meteoric water and precipitated chalcopyrite within the crushed zone at the contact between rhyolite porphyry and wall rock. We suggest that the separation of Cu and Mo in the deposit may be attributed to differences in the chemical properties of Cu and Mo, large‐scale vapor–brine separation of early ore‐forming fluids, and changes in oxygen fugacity.     

Re–Os isotope evidence for mixed source components in carbonate-replacement Pb–Zn–Ag deposits in the Lavrion district,Attica, Greece

The Lavrion ore district contains carbonate-replacement and vein-type Pb–Zn–Ag deposits as well as low-grade porphyry Mo, Cu–Fe skarn, and minor breccia-hosted Pb–Zn–Cu sulfide mineralization. These ore types are spatially related to a Late Miocene granodiorite intrusion (7 to 10 Ma), and various sills and dikes of mafic to felsic composition. Samples of sphalerite and pyrite from the Ilarion carbonate replacement deposit, and galena from Vein 80 (vein-type mineralization) in the Adami deposit show heterogeneous Re–Os values. These values were partially disturbed by hydrothermal activity associated with the formation of hydrothermal veins (e.g., Vein 80). A plot of initial ¹⁸⁷Os/¹⁸⁸Os versus 1/Os_common ratios for pyrite and sphalerite from the Ilarion deposit form a mixing line (r²?=?0.78) between high concentration crustal-like and low concentration mantle-like end-members, or two crustal end-members one of which was more radiogenic than the other. Based on the Re–Os systematics and previously published geological and geochemical evidence, the most plausible explanation for the Re–Os isotope data is that ore-forming components were derived from mixed sources, one of which was a radiogenic crustal source from schists and carbonates probably near intrusion centers and the other, intrusive rocks in the district that are less radiogenic. Although the Re and Os concentrations of galena from Vein 80 are above background values they cannot be used as a chronometer. However, the results of the current study suggest that although pyrite, sphalerite, and galena are poor geochronometers in this ore deposit, due to partial open-system behavior, they still yield valuable information on the origin of the source rocks in the formation of bedded replacement and vein mineralization in the Lavrion district.     

A hydrothermal origin for the large Xinqiao Cu-S-Fe deposit,Eastern China: Evidence from sulfide geochemistry and sulfur isotopes

The Xinqiao Cu-S-Fe deposit in the Tongling ore district, Middle-Lower Yangtze River Valley Metallogenic Belt (MLYB; Eastern China), is located along the northern margin of the Yangtze Craton. The stratiform- and skarn-type Xinqiao mineralization comprises five stages, namely the early skarn (Stage I, garnet and diopside), late skarn (Stage II, epidote-dominated), iron oxides (Stage III, hematite and magnetite), colloform pyrite (Stage IV) and quartz-sulfides (Stage V). There are three pyrite types at Xinqiao, i.e., colloform (Py1; Stage IV), fine-grained (Py2, from Py1 recrystallization; Stage V) and coarse-grained (Py3; Stage V) pyrites.Scanning Electron Microscope (SEM) imagery for Py1 reveals that they are cubic microcrystalline pyrite aggregates, and the EDS and XRD data indicate that some Py1 contain minor siderite impurities. Electron Microprobe Analysis (EMPA) and LA-ICP-MS geochemical data demonstrate that the three pyrite types have relatively high Fe/S ratios and distinctly high Mn, Cu and As concentrations. Compared to Py2 and Py3, Py1 has higher Pb, Bi and Ag, but lower Co, Ni, Se, Cd, Te and Au. Ratios of Fe/S (0.837 to 0.906), Se/Te (2.39 to 14.50) and Co/Ni (0.67 to 4.67) of the Xinqiao pyrites resemble typical hydrothermal pyrites. δ³⁴S_CDT of Py1 (− 0.6‰ to 2.7‰, average 0.58‰), Py2 (1.8‰ to 2.5‰, average 2.1‰) and Py3 (1.9‰ to 4.4‰, average 3.5‰) are close to those of the Xinqiao skarn-type orebodies (1.3‰ to 4.1‰), but distinct from those of the Upper Carboniferous Huanglong Formation limestone (− 9.5‰ to − 15.4‰), suggesting that the three pyrite types (especially Py1) were genetically linked to the Yanshanian (Jurassic-Cretaceous) magmatic-hydrothermal events, with Py1 probably reflecting rapid crystallization during fluid mixing. We interpret that the Xinqiao stratiform mineralization may have been associated with the Jitou quartz diorite stock, as may be the case also for the skarn-type mineralization hosted in the contact between the Yanshanian Jitou stock and the Lower Permian Qixia Formation limestone. Overall, the Xinqiao Cu-S-Fe mineralization may have been generated by the Jurassic-Cretaceous tectono-thermal event in Eastern China.     

Fluid Inclusions and Hydrogen,Oxygen, Sulfur Isotopes of Nuri Cu‐W‐Mo Deposit in the Southern Gangdese,Tibet

The Nuri Cu‐W‐Mo deposit is located in the southern subzone of the Cenozoic Gangdese Cu‐Mo metallogenic belt. The intrusive rocks exposed in the Nuri ore district consist of quartz diorite, granodiorite, monzogranite, granite porphyry, quartz diorite porphyrite and granodiorite porphyry, all of which intrude in the Cretaceous strata of the Bima Group. Owing to the intense metasomatism and hydrothermal alteration, carbonate rocks of the Bima Group form stratiform skarn and hornfels. The mineralization at the Nuri deposit is dominated by skarn, quartz vein and porphyry type. Ore minerals are chalcopyrite, pyrite, molybdenite, scheelite, bornite and tetrahedrite, etc. The oxidized orebodies contain malachite and covellite on the surface. The mineralization of the Nuri deposit is divided into skarn stage, retrograde stage, oxide stage, quartz‐polymetallic sulfide stage and quartz‐carbonate stage. Detailed petrographic observation on the fluid inclusions in garnet, scheelite and quartz from the different stages shows that there are four types of primary fluid inclusions: two‐phase aqueous inclusions, daughter mineral‐bearing multiphase inclusions, CO₂‐rich inclusions and single‐phase inclusions. The homogenization temperature of the fluid inclusions are 280°C–386°C (skarn stage), 200°C–340°C (oxide stage), 140°C–375°C (quartz‐polymetallic sulfide stage) and 160°C–280°C (quartz‐carbonate stage), showing a temperature decreasing trend from the skarn stage to the quartz‐carbonate stage. The salinity of the corresponding stages are 2.9%–49.7 wt% (NaCl) equiv., 2.1%–7.2 wt% (NaCl) equiv._, 2.6%–55.8 wt% (NaCl) equiv. and 1.2%–15.3 wt% (NaCl) equiv., respectively. The analyses of CO₂‐rich inclusions suggest that the ore‐forming pressures are 22.1 M Pa–50.4 M Pa, corresponding to the depth of 0.9 km–2.2 km. The Laser Raman spectrum of the inclusions shows the fluid compositions are dominated in H₂O, with some CO₂ and very little CH₄, N₂, etc. δD values of garnet are between ?114.4‰ and ?108.7‰ and δ¹⁸O_H2O between 5.9‰ and 6.7‰; δD of scheelite range from ?103.2‰ to ?101.29‰ and δ¹⁸O_H2O values between 2.17‰ and 4.09‰; δD of quartz between ?110.2‰ and ?92.5‰ and δ¹⁸O_H2O between ?3.5‰ and 4.3‰. The results indicate that the fluid came from a deep magmatic hydrothermal system, and the proportion of meteoric water increased during the migration of original fluid. The δ³⁴S values of sulfides, concentrated in a rage between ?0.32‰ to 2.5‰, show that the sulfur has a homogeneous source with characteristics of magmatic sulfur. The characters of fluid inclusions, combined with hydrogen‐oxygen and sulfur isotopes data, show that the ore‐forming fluids of the Nuri deposit formed by a relatively high temperature, high salinity fluid originated from magma, which mixed with low temperature, low salinity meteoric water during the evolution. The fluid flow through wall carbonate rocks resulted in the formation of layered skarn and generated CO₂ or other gases. During the reaction, the ore‐forming fluid boiled and produced fractures when the pressure exceeded the overburden pressure. Themeteoric water mixed with the ore‐forming fluid along the fractures. The boiling changed the pressure and temperature, oxygen fugacity, physical and chemical conditions of the whole mineralization system. The escape of CO₂ from the fluid by boiling resulted in scheelite precipitation. The fluid mixing and boiling reduced the solubility of metal sulfides and led the precipitation of chalcopyrite, molybdenite, pyrite and other sulfide.     

Evolution of magmatic-hydrothermal system of the Kalaxiange’er porphyry copper belt and implications for ore formation (Xinjiang,China)

The Kalaxiange’er porphyry copper ore belt is situated in the eastern part of the southern Altai of the Central Asian Orogenic Belt and forms part of a broad zone of Cu porphyry mineralization in southern Mongolia, which includes the Oyu Tolgoi ore district and other copper–gold deposits. The copper ore bodies are spatially associated with porphyry intrusions of granodiorite, quartz diorite, quartz syenite, and quartz monzonite and have a polygenetic (polychromous) origin (magmatic porphyry, hydrothermal, and supergene). The mineralized porphyries are characterized by almost identical REE and trace element patterns. The Zr/Hf and Nb/Ta ratios are similar to those of normal granite produced through the evolution of mantle magma. The low initial Sr isotope ratio I_Sr, varying within a narrow range of values (0.703790–0.704218), corresponds to that of primitive mantle, whereas the εNd(T) value of porphyry varies from 5.8 to 8.4 and is similar to that of MORB. These data testify to the upper-mantle genesis of the parental magmas of ore-bearing porphyry, which were then contaminated with crustal material in an island-arc environment. The isotopic composition of sulfur (unimodal distribution of δ34S with peak values of − 2 to − 4‰) evidences its deep magmatic origin; the few lower negative δ³⁴S values suggest that part of S was extracted from volcanic deposits later. The isotopic characteristics of Pb testify to its mixed crust–upper-mantle origin. According to SHRIMP U–Pb geochronological data for zircon from granite porphyry and granodiorite porphyry, mineralization at the Xiletekehalasu porphyry Cu deposit formed in two stages: (1) Hercynian “porphyry” stage (375.2 ± 8.7 Ma), expressed as the formation of porphyry with disseminated and vein–disseminated mineralization, and (2) Indosinian stage (217.9 ± 4.2 Ma), expressed as superposed hydrothermal mineralization. The Re–Os isotope data on molybdenite (376.9 ± 2.2 Ma) are the most consistent with the age of primary mineralization at the Xiletekehalasu porphyry Cu deposit, whereas the Ar–Ar isotopic age (230 ± 5 Ma) of K-feldspar–quartz vein corresponds to the stage of hydrothermal mineralization. The results show that mineralization at the Xiletekehalasu porphyry Cu deposit was a multistage process which resulted in the superposition of the Indosinian hydrothermal mineralization on the Hercynian porphyry Cu mineralization.     

Geology and genesis of Kafang Cu–Sn deposit,Gejiu district,SW China

Kafang is one of the main ore deposits in the world-class Gejiu polymetallic tin district, SW China. There are three main mineralization types in the Kafang deposit, i.e., skarn Cu–Sn ores, stratiform Cu ores hosted by basalt and stratiform Cu–Sn ores hosted by carbonate. The skarn mainly consists of garnet and pyroxene, and retrograde altered rocks. These retrograde altered rocks are superimposed on the skarn and are composed of actinolite, chlorite, epidote and phlogopite. Major ore minerals are chalcopyrite, pyrrhotite, cassiterite, pyrite and scheelite. Sulfur and Pb isotopic components hint that the sources of different types of mineralization are distinctive, and indicate that the skarn ore mainly originated from granitic magma, whereas the basalt-hosted Cu ores mainly derived from basalt. Microthermometry results of fluid inclusions display a gradual change during the ore-forming process. The homogenization temperature of different types of inclusions continuously decreases from early to late mineralization stages. The salinities and freezing temperatures exhibit similar evolutionary tendencies with the T _{homogenization}, while the densities of the different types keep constant, the majority being less than 1. Oxygen and hydrogen isotopic values (δ¹⁸O and δD) of the hydrothermal fluids fall within ranges of 3.1 to 7.7‰ with an average of 6.15‰, calculated at the corresponding homogenization temperature, and − 73 and − 98‰ with an average of − 86.5‰, respectively. Microthermometry data and H–O isotopes indicate that the ore-forming fluid of the Kafang deposit is mainly derived from magma in the early stage and a mixture of meteoric and magmatic water in late stage. Molybdenite Re–Os age of the skarn type mineralization is 83.4 ± 2.1 Ma, and the stratiform ores hosted by basalt is 84.2 ± 7.3 Ma, which are consistent with the LA-ICP-MS zircon age of the Xinshan granite intrusion (83.1 ± 0.4 Ma). The evidence listed above reflects the fact that different ore styles in the Kafang deposit belong to the same mineralization system.     

In situ trace elements and sulfur isotope analysis of sulfides from the Akiri Cu ± (Ag) deposit,Benue Trough,North-central Nigeria: Implications for ore genesis

The Benue Trough of Nigeria is an intracratonic rift basin hosting several vein-type base metal deposits. The Akiri Cu ± (Ag) deposit represents a distinct sub-class of sediment-hosted Pb-Zn-Cu-Ba mineralization found throughout the Benue Trough. The deposit is hosted in bleached red beds of the Keana Formation and in shale-siltstones and carbonates of the Ezeaku Formation in the Middle Benue Trough, North-Central Nigeria. Mineralization at the Akiri deposit occurs as vein in-fillings in a series of NE-SW and E-W trending faults and fractures in the Early- to Late-Turonian Keana and Eze-Aku sedimentary rocks. To better constrain the sources of ore minerals and structural controls on the formation of this sediment-hosted Cu ± (Ag) mineralization, we report combined geologic, geochemical, mineralogical, and stable isotopic data for the Akiri Cu ± (Ag) deposit. Major ore-stage sulfides at Akiri are chalcopyrite and pyrite, which were accompanied by several types of alteration, including silicification, hematization, limited pyritization, and bleaching of mineralized sandstone bodies. In-situ trace element and sulfur isotopic data distinguishes early-stage pyrite (Py1) from late-stage pyrite (Py2). The late-stage Py2 co-exists with chalcopyrite suggesting coeval precipitation. Early-stage pyrite (Py1) contains lower Ag (avg. 0.04 ppm) but higher Au (avg. 3.03 ppm) than the late-stage pyrite (Py2) (avg. Ag = 2.78 ppm; Au = 0.424 ppm). The δ³⁴S values of the early-stage sulfide (Py1) vary from 19.07‰ to 25.99‰ (avg. 22.20‰), suggesting that sulfur was largely derived from thermochemical reduction (TSR) of seawater sulfate. The δ³⁴S values for co-existing Py2 and chalcopyrite range from 9.83‰ to 11.24‰ (avg. 10.32‰) and from 7.37‰ to 10.69‰ (avg. 8.96‰), respectively, suggesting a derivation of sulfur from TSR of seawater sulfate with contributions from magmatic sulfur. Based on structural features and ore textures, we propose that sulfide precipitation at Akiri was facilitated by sulfur-rich fluids circulating through pre-existing structures (fractures and faults) under fairly high (>200 °C) to moderate (<170 °C) temperature conditions. Geological, mineralogical, geochemical and isotopic data from this study support the classification of the Akiri Cu (+Ag) deposit as an epigenetic sandstone-hosted copper deposit.     

粤北书楼丘铀矿床黄铁矿原位微量元素、 硫同位素组成及矿床成因指示

书楼丘铀矿床作为长江铀矿田重要的组成部分之一,其成矿流体特征、来源及成矿环境研究相对较少.依据黄铁矿晶型特征及其与其他矿物共生组合特征,将书楼丘铀矿床中脉石矿物黄铁矿的形成划分为成矿前期(Py I)、成矿期(PyⅡ)及成矿晚期(PyⅢ)三个时期,成矿期又被划分为成矿早阶段(PyⅡa)和主成矿阶段(PyⅡb).采用激光剥...