Regional Metallogenesis of the Chang’an Gold Ore Deposit in Western Yunnan: Evidences from Fluid Inclusions and Stable Isotopes

<正>The Chang'an gold ore deposit in western Yunnan is located at the southern segment of the Ailaoshan metallogenic belt.The ore bodies are preserved in fractured Ordovician sedimentary clastic rocks.The gold-bearing minerals occur dominantly in sulfide-quartz veins.Fluid inclusion analysis shows that the Chang'an gold ore deposit is characterized by epithermal gold mineralization at temperatures between 200℃and 280℃at a shallow crustal level.The mineralizing fluids have intermediate to low salinity(6%-18%) and low densities(0.72-1.27 g/cm~3).The ore minerals haveδ~(34)S in a range from -13‰to 3.57‰,concentrated from -2.06‰to 3.57‰with an average of 1.55‰.The ~(206)Pb/~(204)Pb,~(207)Pb/~(204)Pb and ~(208)Pb/~(204)Pb values are 18.9977-19.5748,15.7093-15.784,39.3814-40.2004 respectively.These isotope data suggest that the ore-forming elements were mainly derived from mixed crustal and mantle sources.The Chang'an gold ore deposit and Tongchang Cu-Mo deposit are closely related to each other in their spatial distribution and age of formation.They have similar sources of mineralizing elements and identical ore-forming metal elements,and show a close relationship in physical and chemical conditions of mineralization.The two deposits constitute an epithermal-porphyry -skarn type Cu-Mo-Au mineralization system in the Tongchang-Chang'an area,which is related to the Cenozoic high-K alkaline magmatism.     

胶东邓格庄金矿床成因:地质年代学和同位素体系制约

邓格庄金矿地处华北克拉通胶东半岛东部苏鲁超高压带内,黄金储量已超过50t,是胶东牟平-乳山成矿带第二大石英脉型金矿床。矿体产于昆嵛山岩体和荆山群变质岩接触带附近的昆嵛山岩体中,金矿体受控于金牛山断裂带西侧的次级断裂。矿石中的硫-铅-氢-氧同位素值表明成矿流体主要来源于岩浆,具有以地壳为主兼具地幔混合特征,通过深渊断裂发生迁移,在成矿晚期遭受天水混染。围岩昆嵛山二长花岗岩高精度的锆石U-Pb年龄为155. 8Ma,成矿前期蚀变岩中蚀变矿物钾长石和绢云母~(40)Ar-~(39)Ar精确测年结果分别为123Ma和104Ma。结合近年来前人的研究资料,我们建立了胶东金矿集区中生代岩浆岩演化序列,将其划分为160～150Ma、130～110Ma、110～100Ma三个阶段,并给出了大规模爆发式成矿的年龄峰值(120±10Ma)。认为邓格庄金矿既非以变质流体为特征的典型造山型金矿,也非浅成低温热液型金矿,而是伴随华北克拉通岩石圈减薄、软流圈物质上涌、地壳拉张而使壳幔混合流体在浅部以大纵深脉状集中成矿为基本特征的中温岩浆热液型金矿。     

The nature of gold-bearing fluids in Atud gold deposit,Central Eastern Desert,Egypt

Electron microprobe analyses of gold and associated ore minerals as well as stable isotope analyses of sulphide and carbonate minerals were performed in order to determine the metal and fluid sources and temperature of the mineralizing systems to better understand the genesis of the Atud gold deposit hosted in the metagabbro–diorite complex of Gabal Atud (Central Eastern Desert, Egypt). The gold can be classified as electrum (63.6–74.3 wt.% Au and 24.6–26.6 wt.% Ag) and is associated with arsenopyrite and As-bearing pyrite in the main mineralization (gold-sulphides) phase within the main mineralized quartz veins and altered host rocks. Based on the arsenopyrite geothermometer, As-contents (29.3–32.7 atom%) in arsenopyrite point to deposition in the Log ?_S2 and T ranges of ?10.5 to ?5.5 and 305–450°C, respectively, during the main mineralizing phase. Based on the δ³⁴S isotopic compositions of the sulphides, they are originated from magmatic fluids in which the sulphur is either sourced directly from magma or remobilized from the magmatic rocks (gabbroic rocks). On the other hand, calcite formed from fluids having mainly magmatic mixed with variable metamorphic signatures based on its δ¹³C and δ¹⁸O values. This work concluded that the gold-bearing ores at Atud deposit have magmatic sources leaching from the country intrusive rocks during water/rock interactions then remobilized during a metamorphic event. Therefore, the Atud gold deposit is classified as an intrusion-related gold deposit, in which the gabbro–diorite host intrusion acted as the source of metals which were mobilized and deposited as a result of the effects of NW–SE shearing.     

Genesis of the Zhaxikang epithermal Pb-Zn-Sb deposit in southern Tibet,China: Evidence for a magmatic link

The Zhaxikang Pb-Zn-Sb deposit is one of the most important deposits in the Southern Tibet metallogenic belt. Based on field geology, petrography, melt- and fluid inclusions and C-H-O isotopes, we describe and discuss the mineralization, alteration, and their possible link with magmatic fluids. Our results show that the Zhaxikang deposit shares many geological and geochemical similarities with typical intermediate-sulfidation (IS) epithermal deposits. The Pb-Zn-Sb mineralization is closely related to Fe-Mn carbonate- and silicic alterations, which formed the outer rim around the greisen in the Cuonadong Dome. Orebodies occur mainly as structurally-controlled veins and breccia dikes, with major minerals include sphalerite, galena, pyrite, arsenopyrite, and Fe-Mn carbonates. Main stage ore-forming fluids were of medium temperature (214–292 °C), low salinity (2.6–5.3 wt.% NaCl eqv.) and CO₂-bearing.Melt/fluid inclusions in beryl and quartz from the pegmatite indicate that the primary magmatic fluids were derived from the melt-fluid immiscibility. The magmatic fluids were of low salinity (0.2–7.9 wt.% NaCl eqv.), high temperature (298–457 °C) and CO₂-rich, and contained minor CH₄, N₂, C₂H₆, C₃H₈ and C₆H₆. The presence of Mn-Fe carbonates and daughter gahnite minerals in the beryl-hosted inclusions indicates high Mn, Fe and Zn contents in the parental magma and related magmatic fluids. This implies a genetic link between magmatic fluids and the Pb-Zn-Sb mineralization, as also supported by Ar-Ar dating and H-O-C isotopic evidence. We suggest that the Zhaxikang is best classified as an IS epithermal deposit, and the ore-forming fluids are likely to be magma-derived. Boiling of the magmatic fluids led to high-salinity fluids and metal enrichment. High regional geothermal gradient caused by the thermal doming event may have facilitated long distance transportation of magmatic fluids, and led to the formation of a wide alteration zone and distal Pb-Zn-Sb mineralization. The temperature drop and meteoric water involvement may have precipitated the Pb-Zn-Sn minerals in the distal fault systems.     

Helium isotopes in geothermal systems: Iceland,The Geysers,Raft River and Steamboat Springs

Helium isotope ratios have been measured in geothermal fluids from Iceland, The Geysers, Raft River, Steamboat Springs and Hawaii. These ratios have been interpreted in terms of the processes which supply He in distinct isotopic ratios (i.e. magmatic He, ~10 R_a; atmospheric He, R_a; and crustal He, ~0.1 R_a) and in terms of the processes which can alter the isotopic ratio (hydrologic mixing, U-Th series alpha production and weathering release of crustal He, magma aging and tritiugenic addition of ³He). Using this interpretational scheme, Iceland is found to be an area of hot-spot magmatic He implying an active volcanic source although the data are suggestive of high-temperature weathering release of crustal He incorporated in the geothermal fluids. By comparison to fumarolic gases from Hawaii and Juan De Fuca and Cayman Trench basaltic glass samples, The Geysers contains MOR type magmatic He again implying an active volcanic source possibly a “leaky” transform related to the San Andreas Fault System. Raft River contains only crustal He indicating no active volcanic sources. Steamboat Springs He isotope ratios are distinctly less than typical plate margin volcanics but must still have a magmatic source. A preliminary assessment of the cause for this low ratio is made assuming an “aging” magma source.     

岩浆熔融体性质及演化在成矿过程中的作用——以西藏玉龙斑岩铜(钼)矿床为例

玉龙斑岩铜(钼)矿床是亚洲最大的斑岩型铜矿床，包含多种矿化类型，成矿作用复杂。作为典型的斑岩型矿床，岩浆熔融体的性质在玉龙铜矿床的形成过程中起到了至关重要的作用。本文将分别从岩浆熔融体的物理和化学性质出发，解释玉龙矿床为何能成为玉龙成矿带中唯一一个超大型矿床的原因。在熔体演化方面，笔者主要通过对熔体密度、粘度的计算获得有关数据，以了解熔体运移、含矿流体分离的过程，以解释玉龙铜矿床为何能形成如此规模的矿床。     

Chemical,isotopic and mineralogical characteristics of volcanogenic epithermal fluorite deposits on the Permo-Mesozoic foreland of the Andean volcanic arc in Patagonia (Argentina)

Epithermal deposits mined for fluorite in Patagonia, Argentina, are closely related to late Triassic through Jurassic magmatic activity which brought about felsic to intermediate magmatic rocks. The fluorite mineralization in the Patagonian epithermal system resulted from gaseous F-and CO₂-enriched magmas which lead to an explosive phreatomagmatic volcanism, when getting in contact with groundwater near the surface. As a result of these hydrothermal processes, rapid cooling took place in the epithermal mineralization. Changes in the viscosity along with the cooling down of mineralizing fluids caused mottled mineral colors blurring the boundaries between the stages and ore textures.The fluids accountable for the main constituents fluorite, quartz, barite and silica were operative over a vertical extension of roughly 600 m. Their temperature of formation dropped from 379 °C through 64 °C, while the pH decreased from the heat center towards the paleosurface under oxidizing conditions. This steep temperature gradient conducive to the telescoping of mineral associations into each other was accompanied by a rapid loss in CO₂, and a mixing of meteoric and magmatic fluids. Even the boundary between the hypogene and supergene alteration cannot be drawn precisely within the assemblage of Mn oxides, which bridge the gap between hypogene and supergen mineralization. The physical-chemical parameters of the fluids, particularly, the redox conditions did not allow sulfides to be preserved. A classification of the epithermal system as to its degree of sulfidation is based on K-feldspar and kaolinite which are present in significant amounts, whereas APS (aluminum-phosphate-sulfate) minerals are absent. Therefore a categorization as an epithermal fluorite deposit of low- to intermediate sulfidation is justified, because the only mineral of economic interest in the system is fluorite.The data obtained during this joint study render the Patagonian fluorite district a reference type of fluorite in an epithermal system of low- to intermediate sulfidation which are widespread in Argentina, e.g., Sierras Pampeanas, and evolved on part of the stable craton, called Gondwana and which grade into epithermal Au, Ag, In, Pb and Zn deposits.     

西藏甲玛铜多金属矿床流体､成矿物质来源的地球化学约束

甲玛铜多金属矿是西藏冈底斯成矿带中东段勘查程度最高、成矿元素与矿体类型复杂的超大型斑岩-矽卡岩型矿床。前人在控岩-控矿构造、矿床地质、地球化学、矿床模型等方面已经完成了大量的研究工作,但对于矿床成矿机制研究方面尚存不足,特别是流体、成矿物质的来源方面欠缺系统的研究工作和对资料的全面梳理。文章在大量阅研和总结前人研究资料的基础上,以矿区16号勘探线作为典型剖面开展了氧同位素填图,同时对硫同位素进行了必要的样品补充采集。通过综合研究,有证据表明甲玛矿区深部隐伏斑岩体存在岩浆流体的出溶,在此基础上,氢、氧同位素组成表明矿化由早到晚演化过程中,流体由岩浆水向大气降水增加方向演化;同时,氧同位素填图以及流体包裹体平面均一温度分布确定成矿流体源位于矿区zk1616~zk3216一带。此外,S、Si同位素组成均表明了矿区成矿物质主要来源于成矿岩浆岩,而铅同位素的研究进一步说明成矿物质主要来源于冈底斯后碰撞环境下因地壳减薄、地幔上涌导致的壳幔混合作用。文章依据地球化学的研究成果,探讨矿床流体、成矿物质的来源,为甲玛矿床成因、成矿机制研究夯实基础。     

Boron isotope composition of geothermal fluids and borate minerals from salar deposits (central Andes/NW Argentina)

We have measured the boron concentration and isotope composition of regionally expansive borate deposits and geothermal fluids from the Cenozoic geothermal system of the Argentine Puna Plateau in the central Andes. The borate minerals borax, colemanite, hydroboracite, inderite, inyoite, kernite, teruggite, tincalconite, and ulexite span a wide range of δ¹¹B values from −29.5 to −0.3‰, whereas fluids cover a range from −18.3 to 0.7‰. The data from recent coexisting borate minerals and fluids allow for the calculation of the isotope composition of the ancient mineralizing fluids and thus for the constraint of the isotope composition of the source rocks sampled by the fluids. The boron isotope composition of ancient mineralizing fluids appears uniform throughout the section of precipitates at a given locality and similar to values obtained from recent thermal fluids. These findings support models that suggest uniform and stable climatic, magmatic, and tectonic conditions during the past 8 million years in this part of the central Andes. Boron in fluids is derived from different sources, depending on the drainage system and local country rocks. One significant boron source is the Paleozoic basement, which has a whole-rock isotopic composition of δ¹¹B=−8.9±2.2‰ (1 SD); another important boron contribution comes from Neogene-Pleistocene ignimbrites (δ¹¹B=−3.8±2.8‰, 1 SD). Cenozoic andesites and Mesozoic limestones (δ¹¹B≤+8‰) provide a potential third boron source.     

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.     

Isotopic and fluid-inclusion constraints on the formation of polymetallic vein deposits in the central Argentinian Patagonia

The lead isotope compositions of galena and the fluid-inclusion systematics of nine barite-bearing polymetallic (Au, Ag, Pb, Zn) deposits of the central Argentinian Patagonia (Chubut and Rio Negro provinces) have been investigated to constrain the compositions and sources of the mineralizing fluids. Most of the deposits occur as veins, with less common wall-rock disseminations and/or stockworks, and are low-sulfidation epithermal deposits hosted in Jurassic volcanic rocks. Fluid-inclusion homogenization temperatures (Th) from quartz and sphalerite from the deposits fall within the range of 100-300 °C, with the highest measured average temperatures for the most eastern deposits (Mina Angela - 298 °C; Cañadón Bagual - 343 °C). The salinities of the hydrothermal fluids at all deposits were low to moderate (⢪.4 equiv. wt% NaCl). Three groups of ore deposits can be defined on the basis of ²⁰⁶Pb/²⁰⁴Pb ratios for galena and these show a general decrease from west to east (from 18.506 to 18.000). The central Argentinian Patagonia deposits have distinctly less radiogenic lead isotope compositions than similar deposits from Peru and Chile, except for the porphyry copper deposits of central and southern Peru. Galena from the Mina Angela deposit is characterized by very low radiogenic lead isotope compositions (18.000<²⁰⁶Pb/²⁰⁴Pb<18.037 and 38.03<²⁰⁸Pb/²⁰⁴Pb<38.09) and reflects interaction with Precambrian basement. The geographic trend in lead isotope compositions of both galena and whole rocks indicates a crustal contribution which increases eastwards, also reflected in the strontium-neodymium isotope systematics of the host lavas. Finally, due to the lack of precise age determinations for the central Patagonian polymetallic deposits, a potential link with Andean porphyry copper systems remains an open question.     

Magmatic and hydrothermal behavior of uranium in syntectonic leucogranites: The uranium mineralization associated with the Hercynian Guérande granite (Armorican Massif,France)

Most of the hydrothermal uranium (U) deposits from the European Hercynian belt (EHB) are spatially associated with Carboniferous peraluminous leucogranites. In the southern part of the Armorican Massif (French part of the EHB), the Guérande peraluminous leucogranite was emplaced in an extensional deformation zone at ca. 310 Ma and is spatially associated with several U deposits and occurrences. The apical zone of the intrusion is structurally located below the Pen Ar Ran U deposit, a perigranitic vein-type deposit where mineralization occurs at the contact between black shales and Ordovician acid metavolcanics. In the Métairie-Neuve intragranitic deposit, uranium oxide-quartz veins crosscut the granite and a metasedimentary enclave.Airborne radiometric data and published trace element analyses on the Guérande leucogranite suggest significant uranium leaching at the apical zone of the intrusion. The primary U enrichment in the apical zone of the granite likely occurred during both fractional crystallization and the interaction with magmatic fluids. The low Th/U values (< 2) measured on the Guérande leucogranite likely favored the crystallization of magmatic uranium oxides. The oxygen isotope compositions of the Guérande leucogranite (δ¹⁸O_{whole rock} = 9.7–11.6‰ for deformed samples and δ¹⁸O_{whole rock} = 12.2–13.6‰ for other samples) indicate that the deformed facies of the apical zone underwent sub-solidus alteration at depth with oxidizing meteoric fluids. Fluid inclusion analyses on a quartz comb from a uranium oxide-quartz vein of the Pen Ar Ran deposit show evidence of low-salinity fluids (1–6 wt.% NaCl eq.), in good agreement with the contribution of meteoric fluids. Fluid trapping temperatures in the range of 250–350 °C suggest an elevated geothermal gradient, probably related to regional extension and the occurrence of magmatic activity in the environment close to the deposit at the time of its formation. U-Pb dating on uranium oxides from the Pen Ar Ran and Métairie-Neuve deposits reveals three different mineralizing events. The first event at 296.6 ± 2.6 Ma (Pen Ar Ran) is sub-synchronous with hydrothermal circulations and the emplacement of late leucogranitic dykes in the Guérande leucogranite. The two last mineralizing events occur at 286.6 ± 1.0 Ma (Métairie-Neuve) and 274.6 ± 0.9 Ma (Pen Ar Ran), respectively. Backscattered uranium oxide imaging combined with major elements and REE geochemistry suggest similar conditions of mineralization during the two Pen Ar Ran mineralizing events at ca. 300 Ma and ca. 275 Ma, arguing for different hydrothermal circulation phases in the granite and deposits. Apatite fission track dating reveals that the Guérande granite was still at depth and above 120 °C when these mineralizing events occurred, in agreement with the results obtained on fluid inclusions at Pen Ar Ran.Based on this comprehensive data set, we propose that the Guérande leucogranite is the main source for uranium in the Pen Ar Ran and Métairie-Neuve deposits. Sub-solidus alteration via surface-derived low-salinity oxidizing fluids likely promoted uranium leaching from magmatic uranium oxides within the leucogranite. The leached out uranium may then have been precipitated in the reducing environment represented by the surrounding black shales or graphitic quartzites. As similar mineralizing events occurred subsequently until ca. 275 Ma, meteoric oxidizing fluids likely percolated during the time when the Guérande leucogranite was still at depth. The age of the U mineralizing events in the Guérande region (300–275 Ma) is consistent with that obtained on other U deposits in the EHB and could suggest a similar mineralization condition, with long-term upper to middle crustal infiltration of meteoric fluids likely to have mobilized U from fertile peraluminous leucogranites during the Late Carboniferous to Permian crustal extension events.     

A magmatic source of hydrothermal sulfur for the Prominent Hill deposit and associated prospects in the Olympic iron oxide copper-gold (IOCG) province of South Australia

The Prominent Hill deposit is a world-class iron oxide copper–gold (IOCG) deposit in South Australia, characterized by a high Cu/S ratio of the dominant Cu-(Fe) sulfides hosted by hematite breccias. It contains a total resource of 278 Mt of ore at 0.98% Cu and 0.75 g/t Au. Prominent Hill is one of several IOCG deposits and numerous prospects in the Olympic IOCG province that are temporally associated with the 1603–1575 Ma Gawler Range Volcanics, a large igneous province including co-magmatic granitoid intrusions of the Hiltaba Suite. Globally, IOCG deposits share many similar features in terms of their geological environment and mineral association. However, it is not yet clear whether sulfur and copper originate from the same source rocks and which hydrothermal redox processes created the characteristic iron oxide enrichment. Highly variable sulfur isotope compositions of sulfides and sulfates in IOCG deposits have previously been interpreted in terms of diverse sulfur sources that may include contributions from magmatic, sedimentary, seawater or evaporitic sulfur. In order to test these alternatives, we performed a detailed sulfur isotope study of Cu-(Fe) sulfides from Prominent Hill and IOCG prospects nearby. The Prominent Hill deposit shows a wide range in δ³⁴S_V-CDT between − 33.5‰ and 29.9‰ for Cu-(Fe) sulfides, and a narrower range of 4.3‰ to 15.8‰ for barite. Iron sulfides (pyrite, pyrrhotite) show a narrow range in sulfur isotope composition, whereas Cu-bearing sulfides show a much wider range, and more negative δ³⁴S_V-CDT values on average. We propose a two-stage sulfide mineralization model for the IOCG system in the Prominent Hill area, in which all hydrothermal sulfur is ultimately derived from a magmatic source that had a composition of 4.4 ± 2‰. The diversity in sulfur isotope composition can be produced by different fluid evolution pathways along reducing or oxidizing trajectories. A reduced sulfur evolution pathway is responsible for stage I mineralization, when intrusion-derived magmatic-hydrothermal fluids produced early pyrite and minor chalcopyrite at Prominent Hill, and iron ± copper sulfides in regional magnetite skarns and in some pervasively altered volcanic rocks of the Gawler Range Volcanics. Shallow-venting magmatic-hydrothermal fluids and subaerial volcanic gases that became completely oxidized by reaction with atmospheric oxygen produced sulfate and sulfuric acid with a sulfur isotope composition equal to their magmatic source. This highly oxidized ore fluid probably consisted dominantly of water from the hydrosphere, but contained magmatic solute components, notably sulfate, acidity and Cu. Sulfate reduction produced hydrothermal Cu sulfides with a wide range in sulfur isotope compositions from very negative to moderately positive values. Partial reaction of the Cu-rich stage II fluid with earlier stage I sulfides resulted in mixing of sulfur derived from sulfate reduction and from sulfides deposited during stage I. Modeling of the sulfur isotope fractionation processes in response to reducing and oxidizing pathways demonstrates that the entire spectrum of sulfur isotope data from stage I and stage II mineralization can be explained with a single, ultimately magmatic sulfur source. Such a magmatic sulfur source is also adequate to explain the complete spectrum of sulfur isotope data of other IOCG prospects and deposits in the Olympic province, including Olympic Dam. The results of our study challenge the conventional model that suggests the requirement of multiple and compositionally diverse sulfur sources in hematite-breccia hosted IOCG style mineralization.     

Isotope and fluid inclusion geochemistry of the Cangyuan Pb-Zn-Ag polymetallic deposit in Yunnan,SW China

The Cangyuan Pb-Zn-Ag polymetallic deposit is located in the Baoshan Block, southern Sanjiang Orogen. The orebodies are hosted in low-grade metamorphic rocks and skarn in contact with Cenozoic granitic rocks. Studies on fluid inclusions (FIs) of the deposit indicate that the ore-forming fluids are CO₂-bearing, NaCl-H₂O. The initial fluids evolved from high temperatures (462–498 °C) and high salinities (54.5–58.4 wt% NaCl equiv) during the skarn stage into mesothermal (260–397 °C) and low salinities (1.2–9.5 wt% NaCl equiv) during the sulfide stage. The oxygen and hydrogen isotopic compositions (δ¹⁸O_H2O: 2.7–8.8‰; δD: −82 to −120‰) suggest that the ore-forming fluids are mixture of magmatic fluids and meteoric water. Sulfur isotopic compositions of the sulfides yield δ³⁴S values of −2.3 to 3.2‰; lead isotopic compositions of ore sulfides are similar to those of granitic rocks, indicating that the sulfur and ore-metals are derived from the granitic magma. We propose that the Cangyuan Pb-Zn-Ag deposit formed from magmatic hydrothermal fluids. These Cenozoic deposits situated in the west of Lanping-Changdu Basin share many similarities with the Cangyuan in isotopic compositions, including the Laochang, Lanuoma and Jinman deposits. This reveals that the Cenozoic granites could have contributed to Pb-Zn-Cu mineralization in the Sanjiang region despite the abundance of Cenozoic Pb-Zn deposits in the region, such as the Jingding Pb-Zn deposit, that is thought to be of basin brine origin.     

Fluid Inclusions and C?H?O?S?Pb Isotopes: Implications for the Genesis of the Zhuanshanzi Gold Deposit on the Northern Margin of the North China Craton

The Zhuanshanzi gold deposit lies in the eastern section of the Xingmeng orogenic belt and the northern section of the Chifeng‐Chaoyang gold belt. The gold veins are strictly controlled by a NW‐oriented shear fault zone. Quartz veins and altered tectonic rock‐type gold veins are the main vein types. The deposits can be divided into four mineralization stages, and the second and third metallogenic stages are the main metallogenic stages. In this paper, based on the detailed field geological surveys, an analysis of the orebody and ore characteristics, microtemperature measurement of fluid inclusions, the Laser Raman spectrum of the inclusions, determination of C? H? O? S? Pb isotopic geochemical characteristics, and so on were carried out to explore the origin of the ore‐forming fluids, ore‐forming materials, and the genesis of the deposits. The results show that the fluid inclusions can be divided into four types: type I – gas–liquid two‐phase inclusions; type II – gas‐rich inclusions; type III– liquid inclusions; and type IV – CO₂‐containing three‐phase inclusions. However, they are dominated by type Ib – gas liquid inclusions and type IV – three‐phase inclusions containing CO₂. The gas compositions are mainly H₂O and CO₂, indicating that the metallogenic system is a CO₂? H₂O? NaCl system. The homogenization temperature of the ore‐forming fluid evolved from a middle temperature to a low temperature, and the temperature of the fluid was further reduced due to meteoric water mixing during the late stage, as well as a lack of CO₂ components, and eventually evolved into a simple NaCl? H₂O hydrothermal system. C? H? O? S? Pb isotope research proved that the ore‐forming fluids are mainly magmatic water during the early stage, with abundant meteoric water mixed in during the late stage. Ore‐forming materials originated mostly from hypomagma and were possibly influenced by the surrounding rocks, suggesting that the ore‐forming materials were mainly magmatic hydrothermal deposits, with a small amount of crustal component. The fluid immiscibility and the CO₂ and CH₄ gases in the fluids played an active and important role in the precipitation and enrichment of Au during different metallogenic stages. The deposit is considered a magmatic hydrothermal deposit of middle–low temperature.     

In situ Pb and bulk Sr isotope analysis of the Yinchanggou Pb-Zn deposit in Sichuan Province (SW China): Constraints on the origin and evolution of hydrothermal fluids

The Yinchanggou Pb-Zn deposit, located in southwestern Sichuan Province, western Yangtze Block, is stratigraphically controlled by late Ediacaran Dengying Formation and contains >0.3 Mt of metal reserves with 11 wt% Pb + Zn. A principal feature is that this deposit is structurally controlled by normal faults, whereas other typical deposits nearby (e.g. Maozu) are controlled by reverse faults. The origin of the Yinchanggou deposit is still controversial. Ore genetic models, based on conventional whole-rock isotope tracers, favor either sedimentary basin brine, magmatic water or metamorphic fluid sources. Here we use in situ Pb and bulk Sr isotope features of sulfide minerals to constrain the origin and evolution of hydrothermal fluids. The Pb isotope compositions of galena determined by femtosecond LA-MC-ICPMS are as follows: ²⁰⁶Pb/²⁰⁴Pb = 18.17–18.24, ²⁰⁷Pb/²⁰⁴Pb = 15.69–15.71, ²⁰⁸Pb/²⁰⁴Pb = 38.51–38.63. These in situ Pb isotope data overlap with bulk-chemistry Pb isotope compositions of sulfide minerals (²⁰⁶Pb/²⁰⁴Pb = 18.11–18.40, ²⁰⁷Pb/²⁰⁴Pb = 15.66–15.76, ²⁰⁸Pb/²⁰⁴Pb = 38.25–38.88), and both sets of data plotting above the Pb evolution curve of average upper continental crust. Such Pb isotope signatures suggest an upper crustal source of Pb. In addition, the coarse-grained galena in massive ore collected from the deep part has higher ²⁰⁶Pb/²⁰⁴Pb ratios (18.18–18.24) than the fine-grained galena in stockwork ore sampled from the shallow part (²⁰⁶Pb/²⁰⁴Pb = 18.17–18.19), whereas the latter has higher ²⁰⁸Pb/²⁰⁴Pb ratios (38.59–38.63) than the former (²⁰⁸Pb/²⁰⁴Pb = 38.51–38.59). However, both types of galena have the same ²⁰⁷Pb/²⁰⁴Pb ratios (15.69–15.71). This implies two independent Pb sources, and the metal Pb derived from the basement metamorphic rocks was dominant during the early phase of ore formation in the deep part, whereas the ore-hosting sedimentary rocks supplied the majority of metal Pb at the late phase in the shallow part. In addition, sphalerite separated from different levels has initial ⁸⁷Sr/⁸⁶Sr ratios ranging from 0.7101 to 0.7130, which are higher than the ore formation age-corrected ⁸⁷Sr/⁸⁶Sr ratios of country sedimentary rocks (⁸⁷Sr/⁸⁶Sr_200 Ma = 0.7083–0.7096), but are significantly lower than those of the ore formation age-corrected basement rocks (⁸⁷Sr/⁸⁶Sr_200 Ma = 0.7243–0.7288). Again, such Sr isotope signatures suggest that the above two Pb sources were involved in ore formation. Hence, the gradually mixing process of mineralizing elements and associated fluids plays a key role in the precipitation of sulfide minerals at the Yinchanggou ore district. Integrating all the evidence, we interpret the Yinchanggou deposit as a strata-bound, normal fault-controlled epigenetic deposit that formed during the late Indosinian. We also propose that the massive ore is formed earlier than the stockwork ore, and the temporal-spatial variations of Pb and Sr isotopes suggest a certain potential of ore prospecting in the deep mining area.     

Tin partition behavior and implications for the Furong tin ore formation associated with peralkaline intrusive granite in Hunan Province,China

Tin deposits are often closely associated with granitic intrusions. In this study, we analyzed tin partition coefficients between different fluids and melts (\({\text{D}}_{Sn}^{aq.fl./melt}\)) as well as various crystals and melts \({\text{D}}_{Sn}^{aq.fl./melt}\)(\({\text{D}}_{Sn}^{crystal/melt}\)) from the Furong tin deposit associated with the Qitianling A-type granite. Our experimental results indicate that tin partition behavior is affected by the chemical compositions of fluids, melts, and minerals. Tin is prone to partitioning into the residual magma in fractional crystallization or other differential magmatic processes if the magma originated from crustal sources with high alkali content, high volatile content, and low oxygen fugacity. Highly evolved residual peralkaline granitic magma enriched in tin can lead to tin mineralization in a later stage. Furthermore, the volatiles F and Cl in the magma play important roles in tin partitioning behavior. Low F contents in the melt phase and high Cl content in the aqueous fluid phase are favorable factors for tin partitioning in the aqueous fluid phase. High Cl content in the aqueous fluid catalyzes water–rock interaction and leads to the extraction of tin from tin-bearing minerals. All these findings support a hydrothermal origin for the tin deposits. In light of the geotectonic setting, petrochemical characteristics, and mineralizing physicochemical conditions of the Furong tin deposit, it is inferred that the ore-forming fluid of the Furong tin ore deposit could have derived from the Qitianling peralkaline intrusion.     

Petrology,geochemistry and U–Pb geochronology of magmatic rocks from the high-sulfidation epithermal Au–Cu Chelopech deposit,Srednogorie zone,Bulgaria

The Chelopech deposit is one of the largest European gold deposits and is located 60 km east of Sofia, within the northern part of the Panagyurishte mineral district. It lies within the Banat–Srednegorie metallogenic belt, which extends from Romania through Serbia to Bulgaria. The magmatic rocks define a typical calc-alkaline suite. The magmatic rocks surrounding the Chelopech deposit have been affected by propylitic, quartz–sericite, and advanced argillic alteration, but the igneous textures have been preserved. Alteration processes have resulted in leaching of Na₂O, CaO, P₂O₅, and Sr and enrichment in K₂O and Rb. Trace element variation diagrams are typical of subduction-related volcanism, with negative anomalies in high field strength elements (HFSE) and light element, lithophile elements. HFSE and rare earth elements were relatively immobile during the hydrothermal alteration related to ore formation. Based on immobile element classification diagrams, the magmatic rocks are andesitic to dacitic in compositions. Single zircon grains, from three different magmatic rocks spanning the time of the Chelopech magmatism, were dated by high-precision U–Pb geochronology. Zircons of an altered andesitic body, which has been thrust over the deposit, yield a concordant ²⁰⁶Pb/²³⁸U age of 92.21 ± 0.21 Ma. This age is interpreted as the crystallization age and the maximum age for magmatism at Chelopech. Zircon analyses of a dacitic dome-like body, which crops out to the north of the Chelopech deposit, give a mean ²⁰⁶Pb/²³⁸U age of 91.95 ± 0.28 Ma. Zircons of the andesitic hypabyssal body hosting the high-sulfidation mineralization and overprinted by hydrothermal alteration give a concordant ²⁰⁶Pb/²³⁸U age of 91.45 ± 0.15 Ma. This age is interpreted as the intrusion age of the andesite and as the maximum age of the Chelopech epithermal high-sulfidation deposit. ¹⁷⁶Hf/¹⁷⁷Hf isotope ratios of zircons from the Chelopech magmatic rocks, together with published data on the Chelopech area and the about 92-Ma-old Elatsite porphyry–Cu deposit, suggest two different magma sources in the Chelopech–Elatsite magmatic area. Magmatic rocks associated with the Elatsite porphyry–Cu deposit and the dacitic dome-like body north of Chelopech are characterized by zircons with ɛHf_T90 values of ∼5, which suggest an important input of mantle-derived magma. Some zircons display lower ɛHf_T90 values, as low as −6, and correlate with increasing ²⁰⁶Pb/²³⁸U ages up to about 350 Ma, suggesting assimilation of basement rocks during magmatism. In contrast, zircon grains in andesitic rocks from Chelopech are characterized by homogeneous ¹⁷⁶Hf/¹⁷⁷Hf isotope ratios with ɛHf_T90 values of ∼1 and suggest a homogeneous mixed crust–mantle magma source. We conclude that the Elatsite porphyry–Cu and the Chelopech high-sulfidation epithermal deposits were formed within a very short time span and could be partly contemporaneous. However, they are related to two distinct upper crustal magmatic reservoirs, and they cannot be considered as a genetically paired porphyry–Cu and high-sulfidation epithermal related to a single magmatic–hydrothermal system centered on the same intrusion.     

Role of basement in epithermal deposits: The Kushikino and Hishikari gold deposits,southwestern Japan

The magma–ore deposit relationship of most low-sulfidation epithermal ore deposits is still unclear, partly because many stable isotopic studies of such deposits have indicated the predominance of meteoric waters within hydrothermal fluids. However, it is certainly true that hydrothermal systems are ultimately driven by magmatic intrusions, and epithermal gold deposits might therefore be produced by magmatic activity even in deposits having has no obvious links to a magma. We re-examine the genesis of two typical low-sulfidation epithermal gold deposits, the Kushikino and Hishikari deposits, using structural simulations and isotope data.Many epithermal gold deposits including the Kushikino and Hishikari deposits have been discovered in Kyushu, southwestern Japan. The Kushikino deposit comprises fissure-filling veins within Neogene andesitic volcanics that overlie unconformably Cretaceous sedimentary basement. The veins consist of gold- and silver-bearing quartz and calcite with minor amounts of adularia, sericite and sulfides. Although carbon and oxygen isotopic data for the veins indicate a meteoric origin of the ore fluid, finite element simulations suggest that the vein system might have formed in direct response to magma intrusion. In particular, geophysical data suggest that intruding magma has uplifted the basement rocks, thereby producing fractures and veins and a positive Bouguer anomaly, and providing the heat necessary to drive an ore-forming hydrothermal system.The second component of this study has been to investigate the nature and evolution of the Kushikino and Hishikari epithermal systems. Isotope data document the geochemical evolution of the hydrothermal fluids. We conclude that the existence of sedimentary basement rocks at depth might have affected the strontium and carbon isotopic ratios of the Kushikino and Hishikari ore fluids. The ⁸⁷Sr/⁸⁶Sr ratios and δ¹³C–δ¹⁸O trend reveal that major ore veins in the Hishikari deposit can be distinguished from shallow barren veins. It was suggested isotopically that fluids responsible for the barren veins in nearby shallow and barren circulation systems were only controlled by the shallow host rocks. Such multi-isotope systematics provide a powerful tool with which to determine the center of hydrothermal activity and thereby document the evolution of hydrothermal fluids.