Copper–Gold Skarn Mineralization at the Karavansalija Ore Zone,Rogozna Mountain,Southwestern Serbia

Karavansalija ore zone is situated in the Serbian part of the Serbo‐Macedonian magmatic and metallogenic belt. The Cu–Au mineralization is hosted mainly by garnet–pyroxene–epidote skarns and shifts to lesser presence towards the nearby quartz–epidotized rocks and the overlying volcanic tuffs. Within the epidosites the sulfide mineralogy is represented by disseminated cobalt‐nickel sulfides from the gersdorfite‐krutovite mineral series and cobaltite, and pyrite–marcasite–chalcopyrite–base metal aggregates. The skarn sulfide mineralization is characterized by chalcopyrite, pyrite, pyrrhotite, bismuth‐phases (bismuthinite and cosalite), arsenopyrite, gersdorffite, and sphalerite. The sulfides can be observed in several types of massive aggregates, depending on the predominant sulfide phases: pyrrhotite‐chalcopyrite aggregates with lesser amount of arsenopyrite and traces of sphalerite, arsenopyrite–bismuthinite–cosalite aggregates with subordinate sphalerite and sphalerite veins with bismuthinite, pyrite and arsenopyrite. In the overlying volcanoclastics, the studied sulfide mineralization is represented mainly by arsenopyrite aggregates with subordinate amounts of pyrite and chalcopyrite. Gold is present rarely as visible aggregate of native gold and also as invisible element included in arsenopyrite. The fluid inclusion microthermometry data suggest homogenization temperature in the range of roughly 150–400°C. Salinities vary in the ranges of 0.5–8.5 wt% NaCl eq for two‐phase low density fluid inclusions and 15–41 wt% NaCl eq for two‐phase high‐salinity and three‐phase high‐salinity fluid inclusions. The broad range of salinity values and the different types of fluid inclusions co‐existing in the same crystals suggest that at least two fluids with different salinities contributed to the formation of the Cu–Au mineralization. Geothermometry, based on EPMA data of arsenopyrite co‐existing with pyrite and pyrrhotite, suggests a temperature range of 240–360°C for the formation of the arsenopyrite, which overlaps well with the data for the formation temperature obtained through fluid inclusion microthermometry. The sulfur isotope data on arsenopyrite, chalcopyrite, pyrite and marcasite from the different sulfide assemblages (ranging from 0.4‰ to +3.9‰ δ³⁴S_CDT with average of 2.29 δ³⁴S_CDT and standard deviation of 1.34 δ³⁴S_CDT) indicates a magmatic source of sulfur for all of the investigated phases. The narrow range of the data points to a common source for all of the investigated sulfides, regardless of the host rock and the paragenesis. The sulfur isotope data shows good overlap with that from nearby base‐metal deposits; therefore the Cu–Au mineralization and the emblematic base‐metal sulfide mineralization from this metallogenic belt likely share same fluid source.     

Genetic Environment of the Intrusion-related Yuryang Au-Te Deposit in the Cheonan Metallogenic Province, Korea

Abstract. The Yuryang gold deposit, comprising a Te‐bearing Au‐Ag vein mineralization, is located in the Cheonan area of the Republic of Korea. The deposit is hosted in Precambrian gneiss and closely related to pegmatite. The mineralized veins display massive quartz textures, with weak alteration adjacent to the veins. The ore mineralization is simple, with a low Ag/Au ratio of 1.5:1, due to the paucity of Ag‐phases. Ore mineralization took place in two different mineral assemblages with paragenetic time; early Fe‐sulfide mineralization and late Fe‐sulfide and Au‐Te mineralization. The early Fe‐sulfide mineralization (pyrite + sphalerite) occurred typically along the vein margins, and the subsequent Au‐Te mineralization is characterized by fracture fillings of galena, sphalerite, pyrrhotite, Te‐bearing minerals (petzite, altaite, hessite and Bi‐Te mineral) and electrum. Fluid inclusions characteristically contain CO₂ and can be classified into four types (Ia, Ib, IIa and IIb) according to the phase behavior. The pressure corrected temperatures (≥500d?C) indicate that the deposit was formed at a distinctively high temperature from fluids with moderate to low salinity (<12 wt% equiv. NaCl) and CH₄ (1?22 mole %). The sphalerite geo‐barometry yield an estimated pressure about 3.5 ?2.1 kbar. The dominant ore‐deposition mechanisms were CO₂ effervescence and concomitant H₂S volatilization, which triggered sulfidation and gold mineralization. The measured and calculated isotopic compositions of fluids (δ¹⁸O_H2^O = 10.3 to 12.4 %o; δD_H2^O = ‐52 to ‐77 %o) may indicate that the gold deposition originated from S‐type magmatic waters. The physicochemical conditions observed in the Yuryang gold deposit indicate that the Jurassic gold deposits in the Cheonan area, including the Yuryang gold deposit are compatible with deposition of the intrusion‐related Au‐Te veins from deeply sourced fluids generated by the late Jurassic Daebo magmatism.     

Jusa and Barsuchi Log Volcanogenic Massive Sulfide Deposits from the Southern Urals of Russia: Tectonic Setting, Structure and Mode of Formation

The Jusa and Barsuchi Log volcanogenic massive sulfide (VMS) deposits formed along a paleo island arc in the east Magnitogrosk zone of the Southern Urals between ca 398 and 390 Ma. By analogy with the VMS deposits of the west Magnitogrosk zone, they are considered to be Baimak type deposits, which are Zn‐Cu‐Ba deposits containing Au, Ag and minor Pb. Detailed mapping and textural analysis of the two deposits shows that they formed as submarine hydrothermal mounds which were subsequently destroyed on the sea floor under the influence of ocean bottom currents and slumping. Both deposits display a ratio of the length to the maximum width of the deposit >15 and are characterized by ribbon‐like layers composed mainly of bedded ore and consisting principally of altered fine clastic ore facies. The Jusa deposit appears to have formed in two stages: deposition of colloform pyrite followed by deposition of copper–zinc–lead sulfides characterized by the close association of pyrite, chalcopyrite, sphalerite, galena, tennantite, arsenopyrite, marcasite, pyrrhotite, bornite, native gold and electrum and high concentrations of gold and silver. The low metamorphic grade of the east Magnitogorsk zone accounts for the exceptional degree of preservation of these deposits.     

Ore and Skarn Mineralogy of the Yamato Mine,Yamaguchi Prefecture,Japan, with Emphasis on Silver‐, Bismuth‐, Cobalt‐, and Tin‐bearing Sulfides

Assemblages and chemical compositions of ore minerals from the Yamato mine, Yamaguchi Prefecture, Japan, were investigated in detail to clarify its characteristics as a skarn deposit. Special attention was paid to silver‐, bismuth‐, cobalt‐, and tin‐bearing sulfide minerals and native gold at the mine, which are described here for the first time. Samples of arsenopyrite‐dominant massive ore, and garnet‐rich, clinopyroxene‐garnet‐rich, and wollastonite‐bearing skarn ores were collected from the mine dump. Arsenopyrite is the most abundant ore mineral (>80 vol.%) in the massive ore, in association with both As‐poor/free and As‐bearing pyrite. The major ore minerals in the skarn specimens are pyrite, pyrrhotite, arsenopyrite, chalcopyrite, galena, and sphalerite, along with minor argentite, Ag‐Pb‐Bi sulfate, matildite, bismuthinite, native bismuth, molybdenite, scheelite, stannite, stannoidite, cassiterite, cobaltite, gersdorffite, and Co‐rich violarite. In addition, native gold is observed in the interstices of gangue minerals. Based on the mineral assemblages and textures of the specimens examined, the major ore minerals formed in the early stage of mineralization, and the Bi‐, Ag‐, Co‐, Ni‐, As‐ and Sn‐mineralization occurred in the middle stage. Native gold was deposited in the late stage. The estimated formation temperature of the middle mineralization stage was 312±5 °C, according to iron and zinc partitioning between stannite and coexisting sphalerite. The mineralogical properties and mineralization process of the Yamato mine are consistent with those of common skarn‐ and vein‐type ore deposits associated with ilmenite‐series granitoids in the San‐yo and San‐in districts.     

The Arinem Te‐Bearing Gold‐Silver‐Base Metal Deposit,West Java,Indonesia

The vein system in the Arinem area is a gold‐silver‐base metal deposit of Late Miocene (8.8–9.4 Ma) age located in the southwestern part of Java Island, Indonesia. The mineralization in the area is represented by the Arinem vein with a total length of about 5900 m, with a vertical extent up to 575 m, with other associated veins such as Bantarhuni and Halimun. The Arinem vein is hosted by andesitic tuff, breccia, and lava of the Oligocene–Middle Miocene Jampang Formation (23–11.6 Ma) and overlain unconformably by Pliocene–Pleistocene volcanic rocks composed of andesitic‐basaltic tuff, tuff breccia and lavas. The inferred reserve is approximately 2 million tons at 5.7 g t^?1 gold and 41.5 g t^?1 silver at a cut‐off of 4 g t^?1 Au, which equates to approximately 12.5t of Au and 91.4t of Ag. The ore mineral assemblage of the Arinem vein consists of sphalerite, galena, chalcopyrite, pyrite, marcasite, and arsenopyrite with small amounts of pyrrhotite, argentite, electrum, bornite, hessite, tetradymite, altaite, petzite, stutzite, hematite, enargite, tennantite, chalcocite, and covellite. These ore minerals occur in quartz with colloform, crustiform, comb, vuggy, massive, brecciated, bladed and calcedonic textures and sulfide veins. A pervasive quartz–illite–pyrite alteration zone encloses the quartz and sulfide veins and is associated with veinlets of quartz–calcite–pyrite. This alteration zone is enveloped by smectite–illite–kaolinite–quartz–pyrite alteration, which grades into a chlorite–smectite–kaolinite–calcite–pyrite zone. Early stage mineralization (stage I) of vuggy–massive–banded crystalline quartz‐sulfide was followed by middle stage (stage II) of banded–brecciated–massive sulfide‐quartz and then by last stage (stage III) of massive‐crystalline barren quartz. The temperature of the mineralization, estimated from fluid inclusion microthermometry in quartz ranges from 157 to 325°C, whereas the temperatures indicated by fluid inclusions from sphalerite and calcite range from 153 to 218 and 140 to 217°C, respectively. The mineralizing fluid is dilute, with a salinity <4.3 wt% NaCl equiv. The ore‐mineral assemblage and paragenesis of the Arinem vein is characteristically of a low sulfidation epithermal system with indication of high sulfidation overprinted at stage II. Boiling is probably the main control for the gold solubility and precipitation of gold occurred during cooling in stage I mineralization.     

Hydrothermal precipitates associated with bimodal volcanism in the Central Bransfield Strait,Antarctica

Polymetallic sulfide-sulfate mineralization enriched in Pb-Ag-As-Sb-Hg occurs in the Bransfield Strait, a late Tertiary-Quaternary marginal basin close to the Antarctic Peninsula. The mineralization is associated with bimodal volcanism and pelagic and volcaniclastic sediment in rifted continental crust. Hydrothermal precipitates have been recovered from two shallow (1,050–1,000 m water depth) submarine volcanoes (Hook Ridge and Three Sisters) in the Central Bransfield Strait. Mineralization at Hook Ridge consists of polymetallic sulfides, massive barite, and pyrite and marcasite crusts in semilithified pelagic and volcaniclastic sediment. Native sulfur commonly infills void space and cements the volcaniclastic sediment. The polymetallic sulfides are dominated by sphalerite with minor galena, enargite, tetrahedrite-tennantite, pyrite, chalcopyrite, and traces of orpiment cemented by barite and opal-A. The presence of enargite at Hook Ridge, the abundance of native sulfur, and the low Fe content of sphalerite indicate a high sulfur activity of the hydrothermal fluids responsible for mineralization. The sulfur isotopic composition of Hook Ridge precipitates documents the complexity of the sulfur sources in this hydrothermal system with variable influence of biological activity and possibly magmatic contributions. Homogenization temperatures and salinities of fluid inclusions in barite and opal-A suggest that boiling may have affected the hydrothermal fluids during their ascent. The discovery of massive barite-silica precipitates at another shallow marine volcano (Three Sisters volcano) attests to the potential for hydrothermal mineralization at other volcanic edifices in the area. The characteristics of the mineralization in the Bransfield Strait with rifting of continental crust, the presence of bimodal volcanism, including highly evolved felsic volcanic rocks, the association with sediments, and the Pb-Ag-As-Sb-Hg enrichment are similar to the setting of massive sulfide deposits in the Okinawa Trough, and distinct from those of sediment-dominated hydrothermal systems such as Escanaba Trough, Middle Valley, and Guaymas Basin. The geological setting of the Bransfield Strait is also broadly similar to that of some of the largest volcanogenic massive sulfide deposits in the ancient record, such as the Iberian Pyrite Belt.Editorial handling: B. Lehmann     

Polymetallic sulfide ores hosted in Late Permian carbonate at the Alanish locality,northern Iraq: petrography and mineral chemistry

Polymetallic sulfide ores (Zn, Pb, Fe, Cu, Ag, and Cd) found in the Alanish locality of northern Iraq are hosted by dolostone in the Late Permian Chia Zairi Formation. The Alanish locality is one of several Zn–Pb deposits that are widespread in northern Iraq, situated along the northern passive margin of the Arabian plate. This paper describes the ore deposit classification, mineral chemistry, and paragenetic sequence of the area and proposes an ore formation model. We report the presence of acanthite and greenockite for the first time in Iraq. A brine solution derived from the sedimentary basin formed the primary sulfide ore minerals (sphalerite, galena, acanthite, pyrite, chalcopyrite, greenockite, and marcasite). The pre-tectonic mineralization is characterized by replacement textures including (1) high-Fe, low-Zn, dark-colored, coarse-grained sphalerite; (2) deformed anisotropic coarse-grained galena; and, (3) idiomorphic cubes of crushed pyrite. Conversely, the post-tectonic mineralization is characterized by open-space filling textures, including (1) low-Fe, high-Zn, light-colored, fine aggregated sphalerite; (2) fine-grained galena; and, (3) the existence of acanthite and marcasite. Although galena is an Ag carrier, both mineralization phases contained non-argentiferous galena. Non-sulfides (smithsonite, cerussite, and goethite) have replaced older sulfides in many areas due to supergene process. Gangue minerals present are dolomite, calcite, barite, and siderite. Open spaces and cavity filling of small paleo-karsts, replacement, veins, and veinlets are common features of the ore body. Metals were sourced from brines generated in the sedimentary basin, whereas sulfur was derived from nearby evaporates. Sediment compaction and tectonic activity, probably during Late Cretaceous, were the driving forces that squeezed and moved ore-bearing fluids derived from the sedimentary basin. Multiple stages of ore-bearing fluids were epigenetically intruded into the Late Paleozoic dolostone, forming an epigenetic strata-bound Mississippi Valley-type deposit precipitated under a temperature of 120 °C, as indicated by the cadmium fractionation in sphalerite and galena. Dolomitization and tectonic activity provided the necessary permeability for accumulating ores. The main ore body is directly connected to a fault plane and to adjacent dolostone that is frequently fractured and brecciated.     

西秦岭凤太矿集区丝毛岭金矿床地质地球化学特征

西秦岭凤太矿集区丝毛岭金矿床位于八卦庙造山型金矿床西侧5km左右,是一个新探明的剪切带型金矿。其成矿作用过程可分为早期石英-绢云母-硫化物阶段、中期多金属-硫化物阶段和晚期碳酸盐阶段。对早、中期的石英流体包裹体测试结果表明,丝毛岭金矿床成矿流体以富CO2、中温、低盐度为特征,总体上属于中温低盐度CO2-H2O体系,流体包裹体类型的多样性是流体不混溶性的产物。从早阶段到主成矿阶段成矿流体的温度、压力和盐度均有降低,硫逸度增高,有利于金的沉淀富集。H、O、S、C同位素研究结果,以及与八卦庙金矿床的对比分析表明,二者的成矿流体具有相似性和同源性,都是以深部来源为主的多源流体。由于丝毛岭金矿床产出的层位高于八卦庙金矿床,其成矿环境相对开放。     

富碱侵入岩与金成矿关系：云南省姚安金矿床 成矿流体形成演化的微量元素和同位素证据

以产在姚安富碱侵入岩体内外接触带上的姚安金矿床为对象，对成矿流体形成演化过程中的微量元素和S、C同位素地球化学进行了综合研究。研究结果表明，富碱侵入岩成岩过程中分异出的岩浆流体提供了姚安金矿床早期成矿作用所必需的成矿流体；从早期成矿阶段至晚期成矿,民矿流体经历了从以岩浆流体为主的流体体系至以大气降水为主的流体体系的转变。因此，钙碱性侵入岩成岩过程中可分异出成矿流体的过程，也存在于富碱浸入岩的成岩过程中。     

江西大背坞金矿床矿石物质组成及金的赋存状态

大背坞金矿床属贫硫化物（糜棱岩）石英脉型,该矿床有用组分唯有Au,自然金是Au最主要的赋存形式,几乎集中富集了全部Au组分.虽然矿石中有极微量的银金矿,并在方铅矿中发现可能还存在次显微金,但含金量却微不足道.石英、黄铁矿、毒砂是自然金的主要载体.自然金成色高,多以中粗粒裂隙金形式产出,粒间金次之,包裹金较少.本矿床中黄铜矿、方铅矿、闪锌矿不发育,含量少,但它们与自然金关系密切,镜下常常发现与自然金共生赋存于较粗粒的黄铁矿、毒砂等载金矿物中.这3种硫化物是发现富矿化的标志.铅同位素结果表明本金矿成矿物质来源于前震旦纪变质沉积岩,中元古界双桥山群是矿源层.金以络合物的形式迁移.当温度降低（低于300℃）,含矿溶液进入容矿空间压力降低,金发生沉淀.矿化早期石英脉包裹体pH值4.91,Eh值164.52,到矿化主期pH升高到6.38~6.72,Eh降低到57.44,从而使金在溶液中的溶解度大大降低,促使金发生沉淀.     

Orogenic Gold Mineralization in the Qolqoleh Deposit, Northwestern Iran

The Qolqoleh gold deposit is located in the northwestern part of the Sanandai‐Sirjan Zone, northwest of Iran. Gold mineralization in the Qolqoleh deposit is almost entirely confined to a series of steeply dipping ductile–brittle shear zones generated during Late Cretaceous–Tertiary continental collision between the Afro‐Arabian and the Iranian microcontinent. The host rocks are Mesozoic volcano‐sedimentary sequences consisting of felsic to mafic metavolcanics, which are metamorphosed to greenschist facies, sericite and chlorite schists. The gold orebodies were found within strong ductile deformation to late brittle deformation. Ore‐controlling structure is NE–SW‐trending oblique thrust with vergence toward south ductile–brittle shear zone. The highly strained host rocks show a combination of mylonitic and cataclastic microstructures, including crystal–plastic deformation and grain size reduction by recrystalization of quartz and mica. The gold orebodies are composed of Au‐bearing highly deformed and altered mylonitic host rocks and cross‐cutting Au‐ and sulfide‐bearing quartz veins. Approximately half of the mineralization is in the form of dissemination in the mylonite and the remainder was clearly emplaced as a result of brittle deformation in quartz–sulfide microfractures, microveins and veins. Only low volumes of gold concentration was introduced during ductile deformation, whereas, during the evident brittle deformation phase, competence contrasts allowed fracturing to focus on the quartz–sericite domain boundaries of the mylonitic foliation, thus permitting the introduction of auriferous fluid to create disseminated and cross‐cutting Au‐quartz veins. According to mineral assemblages and alteration intensity, hydrothermal alteration could be divided into three zones: silicification and sulfidation zone (major ore body); sericite and carbonate alteration zone; and sericite–chlorite alteration zone that may be taken to imply wall‐rock interaction with near neutral fluids (pH 5–6). Silicified and sulfide alteration zone is observed in the inner parts of alteration zones. High gold grades belong to silicified highly deformed mylonitic and ultramylonitic domains and silicified sulfide‐bearing microveins. Based on paragenetic relationships, three main stages of mineralization are recognized in the Qolqoleh gold deposit. Stage I encompasses deposition of large volumes of milky quartz and pyrite. Stage II includes gray and buck quartz, pyrite and minor calcite, sphalerite, subordinate chalcopyrite and gold ores. Stage III consists of comb quartz and calcite, magnetite, sphalerite, chalcopyrite, arsenopyrite, pyrrhotite and gold ores. Studies on regional geology, ore geology and ore‐forming stages have proved that the Qolqoleh deposit was formed in the compression–extension stage during the Late Cretaceous–Tertiary continental collision in a ductile–brittle shear zone, and is characterized by orogenic gold deposits.     

新疆哈密卡拉塔格块状硫化物矿床金银赋存状态研究

新疆哈密红海黄土坡VMS矿床位于东天山卡拉塔格隆起带,是卡拉塔格矿集区内新发现的块状硫化物矿床。矿体产于卡拉塔格隆起带核部火山沉积岩建造中,具有典型的VMS型矿床“上层下脉”二元结构特征。该矿床中含金硫化物矿石主要有块状黄铁矿黄铜矿、块状黄铁矿黄铜矿闪锌矿、块状黄铁矿闪锌矿黄铜矿和块状闪锌矿。文中在对各类含金硫化物矿石进行详细的矿相学研究基础上,结合扫描电子显微镜与能谱仪联用技术(SEM/EDS),对硫化物样品中金、银的赋存状态进行研究。结果表明,4种块状硫化物中的主要矿物形成于多个期次,主要包括VMS成矿期(黄铁矿阶段、闪锌矿黄铜矿黝铜矿方铅矿阶段、石英重晶石阶段)、热液叠加期(石英黄铁矿黄铜矿闪锌矿方铅矿阶段)和表生期(铜蓝纤铁矿阶段)。矿区首次发现4颗金银金属互化物(银金矿、碲银矿),其较大的化学成分差异指示了热液环境由中酸性中性转变为更有利于Au、Ag迁移沉淀的偏碱性。后期的偏碱性热液对VMS成矿期形成矿物产生了交代作用,使得Au、Ag活化再富集。由于后期热液叠加改造,红海VMS型矿床中Au、Ag不仅赋存于VMS成矿期后期中低温闪锌矿黄铜矿阶段,也赋存于VMS成矿期早期中高温黄铁矿阶段,并贯穿整个热液叠加期。各含金矿物组合中除4颗金银金属互化物外Au多呈显微不可见状态,推测Au、Ag主要以原子或离子形式赋存于矿物晶格中或矿物空位处。     

Hydrothermal Alteration and Cu-Au Mineralization at Nena High Sulfidation-type Deposit, Frieda River, Papua New Guinea

Abstract. The Nena Cu‐Au deposit, located in the Frieda River mineral district of northwestern mainland Papua New Guinea, is a composite structurally‐lithologically controlled high sulfidation (HS) system. Its hydrothermal alteration and Cu‐Au mineralization are presented in this paper. Initially propylitized andesitic volcanics veined by epithermal quartz were pervasively superimposed by zoned HS alteration. The zonation grades from vuggy silica core to sulfur‐rich, pyritic silica‐alunite halo followed by pyrophyllite‐dickite‐kaolinite interval and finally to thin illite‐smectite margin, suggesting progressive decrease in temperature and increase in pH. This zonation is enveloped by chlorite‐epidote‐calcite‐gypsum alteration. The acid altered rocks were then invaded by multiple phases of pyrite, subsequently crosscut by quartz, vein alunite and barite. Then sequential deposition of bladed covellite, enargite, luzonite and stibioluzonite occurred from the NW to the SE portions of the deposit, forming a zonation suggestive of progressive decrease in temperature, sulfur fugacity and sulfidation stage. Most ore mineralization occurs in the vuggy silica core. Gold mineralization commenced from the transition of enargite to luzonite and continued throughout the stibioluzonite stage. Associated with gold deposition are Au‐rich pyrite, tennantite‐tetrahedrite, chalcopyrite‐bornite, native tellurium, electrum, calaverite, bismuthinite and galena. Native sulfur occupied the remaining cavities and represents the waning stage of the hydrothermal system. Fluid inclusions studies distinguished magmatic (>300–350d?C, 9–15 wt% NaCl equiv.) and meteoric (<150–200d?C, 1–2 wt% NaCl equiv.) fluids (Holzberger et al., 1996). Temperatures and salinities of fluid inclusions from barite associated with Cu sulfides show a general decrease from NW (330d?C, 9–15 wt% NaCl equiv.) to SE (172d?C, 10 wt% NaCl equiv.) parts of the deposit, indicating gradual entrainment of ground water (Hitchman and Espi, 1997). Interaction of magmatic fluids with meteoric water accompanied by changes in temperature, salinity, acidity and oxidation state of the resultant fluids is interpreted to have been the main cause of metal precipitation. Finally, supergene processes generated Au zone with an underlying chalcocite‐covellite‐digenite blanket over the primary sulfides at depth. Gold occurs as lattice constituent in scorodite, limonite‐goethite and jarosite. Chalcocite is more abundant and widespread than other Cu sulfides. Acidic fluids deposited powdery alunite and kaolinite, vein alunite and amorphous silica. Weakly secondary biotite‐quartz altered porphyry located below the known HS Cu‐Au deposit contains chalcopyrite‐bornite and is overprinted by quartz‐alunite‐pyro‐phyllite‐pyrite assemblage. This feature indicates close temporal, spatial and genetic relation between the two deposit types.     

Diverse Range of Mineralization Induced by Phase Separation of Hydrothermal Fluid: Case Study of the Yonaguni Knoll IV Hydrothermal Field in the Okinawa Trough Back-Arc Basin

The Yonaguni Knoll IV hydrothermal vent field (24°51′N, 122°42′E) is located at water depths of 1370–1385 m near the western edge of the southern Okinawa Trough. During the YK03–05 and YK04–05 expeditions using the submersible Shinkai 6500, both hydrothermal precipitates (sulfide/sulfate/carbonate) and high temperature fluids (Tmax = 328°C) presently venting from chimney‐mound structures were extensively sampled. The collected venting fluids had a wide range of chemistry (Cl concentration 376–635 mmol kg^?1), which is considered as evidence for sub‐seafloor phase separation. While the Cl‐enriched smoky black fluids were venting from two adjacent chimney‐mound structures in the hydrothermal center, the clear transparent fluids sometimes containing CO₂ droplet were found in the peripheral area of the field. This distribution pattern could be explained by migration of the vapor‐rich hydrothermal fluid within a porous sediment layer after the sub‐seafloor phase separation. The collected hydrothermal precipitates demonstrated a diverse range of mineralization, which can be classified into five groups: (i) anhydrite‐rich chimneys, immature precipitates including sulfide disseminations in anhydrite; (ii) massive Zn‐Pb‐Cu sulfides, consisting of sphalerite, wurtzite, galena, chalcopyrite, pyrite, and marcasite; (iii) Ba‐As chimneys, composed of barite with sulfide disseminations, sometimes associated with realgar and orpiment overgrowth; (iv) Mn‐rich chimneys, consisting of carbonates (calcite and magnesite) and sulfides (sphalerite, galena, chalcopyrite, alabandite, and minor amount of tennantite and enargite); and (v) pavement, silicified sediment including abundant native sulfur or barite. Sulfide/sulfate mineralization (groups i–iii) was found in the chimney–mound structure associated with vapor‐loss (Cl‐enriched) fluid venting. In contrast, the sulfide/carbonate mineralization (group iv) was specifically found in the chimneys where vapor‐rich (Cl‐depleted) fluid venting is expected, and the pavement (group v) was associated with diffusive venting from the seafloor sediment. This correspondence strongly suggests that the subseafloor phase separation plays an important role in the diverse range of mineralization in the Yonaguni IV field. The observed sulfide mineral assemblage was consistent with the sulfur fugacity calculated from the FeS content in sphalerite/wurtzite and the fluid temperature for each site, which suggests that the shift of the sulfur fugacity due to participation of volatile species during phase separation is an important factor to induce diverse mineralization. In contrast, carbonate mineralization is attributed to the significant mixing of vapor‐rich hydrothermal fluid and seawater. A submarine hydrothermal system within a back‐arc basin in the continental margin may be considered as developed in a geologic setting favorable to a diverse range of mineralization, where relatively shallow water depth induces sub‐seafloor phase separation of hydrothermal fluid, and sediment accumulation could enhance migration of the vapor‐rich hydrothermal fluid.     

Genesis of the Changba–Lijiagou Giant Pb-Zn Deposit, West Qinling, Central China: Constraints from S-Pb-C-O isotopes

The extensive Changba-Lijiagou Pb-Zn deposit is located in the north of the Xihe–Chengxian ore cluster in West Qinling. The ore bodies are mainly hosted in the marble, dolomitic marble and biotite-calcite-quartz schist of the Middle Devonian Anjiacha Formation, and are structurally controlled by the fault and anticline. The ore-forming process can be divided into three main stages, based on field geological features and mineral assemblages. The mineral assemblages of hydrothermal stage I are pale-yellow coarse grain, low Fe sphalerite, pyrite with pits, barite and biotite. The mineral assemblages of hydrothermal stage II are black-brown cryptocrystalline, high Fe shalerite, pyrite without pits, marcasite or arsenopyrite replace the pyrite with pits, K-feldspar. The features of hydrothermal stage III are calcite-quartz-sulfide vein cutting the laminated, banded ore body. Forty-two sulfur isotope analyses, twenty-five lead isotope analyses and nineteen carbon and oxygen isotope analyses were determined on sphalerite, pyrite, galena and calcite. The δ34 S values of stage I(20.3 to 29.0‰) are consistent with the δ34 S of sulfate(barite) in the stratum. Combined with geological feature, inclusion characteristics and EPMA data, we propose that TSR has played a key role in the formation of the sulfides in stage I. The δ34 S values of stage II sphalerite and pyrite(15.1 to 23.0‰) are between sulfides in the host rock, magmatic sulfur and the sulfate(barite) in the stratum. This result suggests that multiple S reservoirs were the sources for S2-in stage II. The δ34 S values of stage III(13.1 to 22‰) combined with the structure of the geological and mineral features suggest a magmatic hydrothermal origin of the mineralization. The lead isotope compositions of the sulfides have 206 Pb/204 Pb ranging from 17.9480 to 17.9782, 207 Pb/204 Pb ranging from 15.611 to 15.622, and 208 Pb/204 Pb ranging from 38.1368 to 38.1691 in the three ore-forming stages. The narrow and symmetric distributions of the lead isotope values reflect homogenization of granite and mantle sources before the Pb-Zn mineralization. The δ13 CPDB and δ18 OSMOW values of stage I range from-0.1 to 2.4‰ and from 18.8 to 21.7‰. The values and inclusion data indicate that the source of fluids in stage I was the dissolution of marine carbonate. The δ13 CPDB and δ18 OSMOW values of stage II range from-4 to 1‰ and from 12.3 to 20.3‰, suggesting multiple C-O reservoirs in the Changba deposit and the addition of mantle-source fluid to the system. The values in stage III are-3.1‰ and 19.7‰, respectively. We infer that the process of mineralization involved evaporitic salt and sedimentary organic-bearing units interacting through thermochemical sulfate reduction through the isotopic, mineralogy and inclusion evidences. Subsequently, the geology feature, mineral assemblages, EPMA data and isotopic values support the conclusion that the ore-forming hydrothermal fluids were mixed with magmatic hydrothermal fluids and forming the massive dark sphalerite, then yielding the calcite-quartz-sulfide vein ore type at the last stage. The genesis of this ore deposit was epigenetic rather than the previously-proposed sedimentary-exhalative(SEDEX) type.     

Volcanogenic and tectonic features of the Rakkejaur sulfide deposit,Skellefte district,Sweden

The Rakkejaur volcanogenic massive sulfide deposit is conformably situated in a transition zone between Proterozoic pyroclastic and overlying clastic sedimentary rocks. Ore and host rocks are isoclinally folded and slightly overturned. Two distinct types of mineralization occur: Cu-bearing stringers and disseminations, and Zn-rich stratiform banded massive sulfides. Precipitation of stratiform ore was concurrent with late volcanism and continued during the early stages of clastic sedimentation. Pyroclastic debris containing fragments of the underlying stringer-mineralized metavolcanic rocks were deposited in the lower parts of the massive sulfides. Banding of the stratiform massive ore is evidenced by alternating concentrations of pyrite and sphalerite and by interlayered sedimentary strata. Slumping and synsedimentary fragmentation of the massive sulfides took place locally. Epigenetic stringer mineralization was emplaced in two separate conduits located in the footwall metavolcanic rocks. Both mineralized vents are in contact with and beneath the same cap of massive sulfides.Zn, Pb, Ag, and Sb grades are elevated in the banded ore and tend to increase with stratigraphic and lateral distance from the zones of stringer mineralization. Gold occurs in association with arsenic or in amalgam, and each assemblage displays different distribution patterns. Most of the gold is contained in the stratiform ore where distal areas generally show higher Au/As ratios. The Au-As assemblage, however, occurs within one of the conduit zones and in close proximity to the other conduit within the massive sulfides. The ore-forming processes resulted in metasomatic alteration of the footwall rocks, mainly by introduction of Mg and Fe and depletion of Na.     

Mineralogy,Sulfur Isotope and Fluid Inclusion Studies of Hydrothermal Ore at the Hakurei Deposit,Bayonnaise Knoll,Izu‐Bonin Arc

Sulfide and sulfate ore samples collected from the Hakurei deposit of the Bayonnaise knoll were examined for the occurrence and chemical composition of minerals, including the sulfur isotopes and the microthermometry of fluid inclusions. Massive sulfide ore, mineralized volcanic rock, and anhydrite ore occur in descending order, from the seafloor to the bottom of the cored sample. The massive sulfide ore is dominated by sphalerite and accompanied by tennantite, chalcopyrite, and pyrite with lesser amounts of galena, enargite, and covellite. Amorphous silica is commonly precipitated on the surface of the sulfide minerals. As‐bearing minerals such as tennantite, enargite, and luzonite are common, while galena and Sb‐rich tetrahedrite are scarce. The mineral abundance and chemical composition of the minerals differs from that found in chimneys of the deposit. The sulfur isotope compositions in the minerals are +3.1–5.2‰ for sulfides and +19.6–21.8‰ for sulfate minerals. The homogeneous nature of the sulfur isotopes suggests that sulfur incorporated in the Hakurei deposit came from the reduction of aqueous sulfate in seawater.     

Geology,Mineralogy, Geochronology,and Sulfur Isotope Constraints on the Genesis of the Luanling Gold Telluride Deposit,Western Henan Province,Central China

The Luanling gold telluride deposit in the Xiong'ershan region is located in the southern margin of the North China Craton. The deposit formed in four stages, that is, an early pyrite‐quartz stage (I), a pyrite‐molybdenite stage (II), a sulfide‐telluride‐gold stage (III), and a late carbonate stage (IV). Six species of telluride in stage (III) are recognized, including hessite, altaite, petzite, unidentified Au‐Ag‐Te mineral, empressite, and unidentified Ag‐Te‐S mineral. Gold occurs mostly as native gold and electrum along the microfractures of sulfides or the contact between sulfide and telluride. The mineralization temperature of stage I and stage III ranges from 296 to 377°C and 241 to 324°C, respectively. Tellurides in stage III precipitate at the log?_S2 from ?14.3 to ?7.3 and log?_Te2 from ?17.4 to ?9.4. The ores were formed in an oxidizing environment. The Re‐Os model ages of molybdenite are 162–164 Ma, which indicate that the main ore formation stage was in the Late Jurassic. The Re contents of five molybdenite samples from the Luanling deposit have a range of 36.32–81.95 ppm, except for one large value of 220 ppm, which indicates that the ore‐forming materials are mainly derived from a crustal‐dominated source. The δ³⁴S values of sulfides range from ?17.6 to ?6.2‰, whereas those of sulfates are from 6.8 to 11.5‰. The δ³⁴S_∑S value of the ore‐forming system is 0.0–3.7‰, indicating that the sulfur of the Luanling deposit derived from a deep igneous source. Mineral association and isotope data of the Luanling deposit, together with its geodynamic setting, imply that this deposit belongs to a part of the metallogenic system of the Nannihu‐Sandaozhuang, Shangfangou porphyry molybdenum deposits, and the Late Jurassic granitic intrusions.     

黑龙江省宁安市英城子金矿床地质特征及成因研究

英城子金矿床位于兴蒙造山带东缘,矿床产于近东西向韧性脆性剪切带（靡棱岩带）内,矿体主要呈透镜状、似层状和脉状产出.矿石矿物主要为黄铁矿、闪锌矿和黄铜矿,主要结构为交代结构、乳滴状结构、半自形-他形结构,主要构造为浸染状构造、脉状构造、条带状构造.成矿作用先后经历了4个阶段：石英-毒砂-黄铁矿阶段、石英-黄铁矿阶段、石英-多金属硫化物阶段和石英-方解石阶段.成矿流体总体属于中温、低盐度、低密度的CO₂-CH₄-H₂O体系.英城子金矿床与国内外典型的造山型金矿相比具有诸多相似之处,其成因类型属于造山型金矿.     

Ore-microscopic and geochemical characteristics of gold-bearing sulfide minerals,El Sid Gold mine,Eastern Desert,Egypt

Gold deposits at El Sid are confined to hydrothermal quartz veins which contain pyrite, arsenopyrite, sphalerite and galena. These veins occur at the contact between granite and serpentinite and extend into the serpentinite through a thick zone of graphite schist. Gold occurs in the mineralized zone either as free gold in quartz gangue or dissolved in the sulfide minerals. Ore-microscopic study revealed that Au-bearing sulfides were deposited in two successive stages with early pyrite and arsenopyrite followed by sphalerite and galena. Gold was deposited during both stages, largely intergrown with sphalerite and filling microfractures in pyrite and arsenopyrite.Spectrochemical analyses of separated pyrite, arsenopyrite, sphalerite and galena showed that these sulfides have similar average Au contents. Pyrite is relatively depleted in Ag and Te. This suggests that native gold was deposited in the early stage of mineralization. Arsenopyrite and galena show relatively high concentrations of Te. They are also respectively rich in Au and Ag. Tellurides are, thus, expected to be deposited together with arsenopyrite and galena.