Formation of Strata—bound Ore Deposits in China：Studies on Fluid Inclusions

Fluid inclusion studies were made on the basis of the geological data on the strata-bound ore de-posits of China including those of Pb,Zn,Au,Ag,Sb,U,Hg,W,quartz-crystal and sparry-calcite.An attempt was made to approach the model of formation for each type of ore depos-its by considering the material sources,the migration of fluids and the conditions of mineralization.It is found that ore-forming fluids (especially H2O)originate as heated underground water reacts with the wallrocks and dissolves Na^ ,Ca^2 ,K^ ,Cl^ ,HCl^- and Mg^2 .The ore fluids are mainly of NaCl-Ca-HCO3-H2O system with salinities ranging from 4to 14wt.%.NaCl equivalent and densities ranging from 0.9 to 1.0g/cm^3.It may be concluded that the deposits were formed at temperatures ranging from 150 to 250℃ under pressures from 300 to 1000 bars.Ore deposition may have been controlled by temperature and pressure or by the mixing among different fluids.     

Geological and geochemical characteristics of the Baogudi Carlin-type gold district (Southwest Guizhou,China) and their geological implications

The newly discovered Baogudi gold district is located in the southwestern Guizhou Province, China, where there are numerous Carlin-type gold deposits. To better understand the geological and geochemical characteristics of the Baogudi gold district, we carried out petrographic observations, elemental analyses, and fluid inclusion and isotopic composition studies. We also compared the results with those of typical Carlin-type gold deposits in southwestern Guizhou. Three mineralization stages, namely, the sedimentation diagenesis, hydrothermal (main-ore and late-ore substages), and supergene stages, were identified based on field and petrographic observations. The main-ore and late-ore stages correspond to Au and Sb mineralization, respectively, which are similar to typical Carlin-type mineralization. The mass transfer associated with alteration and mineralization shows that a significant amount of Au, As, Sb, Hg, Tl, Mo, and S were added to mineralized rocks during the main-ore stage. Remarkably, arsenic, Sb, and S were added to the mineralized rocks during the late-ore stage. Element migration indicates that the sulfidation process was responsible for ore formation. Four types of fluid inclusions were identified in ore-related quartz and fluorite. The main-ore stage fluids are characterized by an H₂O–NaCl–CO₂–CH₄ ± N₂ system, with medium to low temperatures (180–260 °C) and low salinity (0–9.08% NaCl equivalent). The late-ore stage fluids featured H₂O–NaCl ± CO₂ ± CH₄, with low temperature (120–200 °C) and low salinity (0–7.48% NaCl equivalent). The temperature, salinity, and CO₂ and CH₄ concentrations of ore-forming fluids decreased from the main-ore stage to the late-ore stage. The calculated δ¹³C, δD, and δ¹⁸O values of the ore-forming fluids range from − 14.3 to − 7.0‰, −76 to −55.7‰, and 4.5–15.0‰, respectively. Late-ore-stage stibnite had δ³⁴S values ranging from − 0.6 to 1.9‰. These stable isotopic compositions indicate that the ore-forming fluids originated mainly from deep magmatic hydrothermal fluids, with minor contributions from strata. Collectively, the Baogudi metallogenic district has geological and geochemical characteristics that are typical of Carlin-type gold deposits in southwest Guizhou. It is likely that the Baogudi gold district, together with other Carlin-type gold deposits in southwestern Guizhou, was formed in response to a single widespread metallogenic event.

     

湘西层控金矿床成因机制的研究

流体包裹体的研究表明,湘西层控金矿床为中低温热液矿床,矿床在弱还原、弱碱性的成矿流体中形成,成矿流体为变质水与建造水混合而成。在流体中金主要以[Au(HS)~-]络离子形式运移,流体温度及pH值的改变是导致金沉淀的主要因素。流体包裹体的研究还揭示,成矿能量主要由雪峰造山作用提供。元素地球化学的研究则证实,湘西元古界是典型的Au-Sb-W含矿建造,它为湘西层控金矿床的形成提供了物质基础。本文的研究显示,湘西层控金矿床的成矿作用是中低温开放体系水、岩反应过程。     

Physicochemical factors of formation of Au-As,Au-Sb,and Ag-Sb deposits

The physicochemical formation conditions of Au-As, Au-Sb, and Ag-Sb ores characterized by similar paragenetic mineral assemblages and sets of major ore elements but differing in their proportions have been studied. The composition of the solutions filling fluid inclusions in minerals of Au-Sb deposits, combined with mineralogical and geochemical data, indicates that these deposits were formed from a near-neutral to alkalescent chloride-sulfide (<5 wt % NaCl) solution. Au-As and Au-Sb deposits were formed from fluids of the same type, consisting of a predominately CO₂-CH₄ gas phase with N₂ and a low-saline chloride-sulfide solution, where Au and Ag were predominantly transported as dihydrosulfide species and Sb as sulfide and hydroxy complexes. Superimposed minerals of the sulfide-sulfosalt stage that precipitated from chloride-rich solutions (up to 30 wt % NaCl equiv), which contained Ca and Fe chlorides in addition to NaCl, are identified at some Au-Sb deposits. These solutions are similar in composition to the ore-forming fluids of Ag-Sb deposits. Chloride complexes are dominant Au and Ag species in acid chloride-rich solutions of Ag-Sb deposits (up to 38 wt % NaCl equiv), while chloride and hydroxy complexes are characteristic of Sb. These solutions are distinguished by high concentrations of Ag, Sb, Cu, Fe, Mn, Bi, Pb, and Zn. The mineralogical and geochemical specialization of Ag-Sb ore is caused by chemical features of highly concentrated chloride solutions enriched in Ag, Sb, and Cu and by a relatively low Au content within the pH interval 3.5–4.0 (10^?6 m). The factors controlling formation of Au-As deposits are a high capacity of a low-chloride sulfide solution with respect to metals and a high Au concentration therein (two orders higher than that of solutions of Ag-Sb deposits). The enrichment of the pyrite-arsenopyrite paragenetic assemblage in gold is a result of juxtaposed stability fields of native gold, arsenopyrite, and pyrite and their mass deposition with a decrease in temperature from 400 to 300°C. The main cause of the specific mineralogy and geochemistry of Au-Sb deposits is a high metal capacity of a near-neutral low-chloride sulfide fluid with respect to Sb, Au, and Ag, but a low Ag content. The mineralogical and fluid inclusion data combined with computer thermodynamic simulation allowed us to establish the factors of ore formation at P-T-X parameters close to natural conditions and made it possible to characterize the joint deposition of gold and silver in quantitative terms.     

Geology and mineralization of the Duobaoshan supergiant porphyry Cu-Au-Mo-Ag deposit (2.36 Mt) in Heilongjiang Province,China: A review

The reserves of the Duobaoshan porphyry Cu-Au-Mo-Ag deposit(also referred to as the Duobaoshan porphyry Cu deposit) ranks first among the copper deposits in China and 33rd among the porphyry copper deposits in the world. It has proven resources of copper(Cu), molybdenum(Mo), gold(Au), and silver(Ag) of 2.28×10⁶ t, 80×10³ t, 73 t, and 1046 t, respectively. The major characteristics of the Duobaoshan porphyry Cu deposit are as follows. It is located in a zone sandwiched by th...     

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。     

Paragenesis and geochemistry of ore minerals in the epizonal gold deposits of the Yangshan gold belt,West Qinling,China

Six epizonal gold deposits in the 30-km-long Yangshan gold belt, Gansu Province are estimated to contain more than 300 t of gold at an average grade of 4.76 g/t and thus define one of China's largest gold resources. Detailed paragenetic studies have recognized five stages of sulfide mineral precipitation in the deposits of the belt. Syngenetic/diagenetic pyrite (Py₀) has a framboidal or colloform texture and is disseminated in the metasedimentary host rocks. Early hydrothermal pyrite (Py₁) in quartz veins is disseminated in metasedimentary rocks and dikes and also occurs as semi-massive pyrite aggregates or bedding-parallel pyrite bands in phyllite. The main ore stage pyrite (Py₂) commonly overgrows Py₁ and is typically associated with main ore stage arsenopyrite (Apy₂). Late ore stage pyrite (Py₃), arsenopyrite (Apy₃), and stibnite occur in quartz ± calcite veins or are disseminated in country rocks. Post-ore stage pyrite (Py₄) occurs in quartz ± calcite veins that cut all earlier formed mineralization. Electron probe microanalyses and laser ablation-inductively coupled plasma mass spectrometry analyses reveal that different generations of sulfides have characteristic of major and trace element patterns, which can be used as a proxy for the distinct hydrothermal events. Syngenetic/diagenetic pyrite has high concentrations of As, Au, Bi, Co, Cu, Mn, Ni, Pb, Sb, and Zn. The Py₀ also retains a sedimentary Co/Ni ratio, which is distinct from hydrothermal ore-related pyrite. Early hydrothermal Py₁ has high contents of Ag, As, Au, Bi, Cu, Fe, Sb, and V, and it reflects elevated levels of these elements in the earliest mineralizing metamorphic fluids. The main ore stage Py₂ has a very high content of As (median value of 2.96 wt%) and Au (median value of 47.5 ppm) and slightly elevated Cu, but relatively low values for other trace elements. Arsenic in the main ore stage Py₂ occurs in solid solution. Late ore stage Py₃, formed coevally with stibnite, contains relatively high As (median value of 1.44 wt%), Au, Fe, Mn, Mo, Sb, and Zn and low Bi, Co, Ni, and Pb. The main ore stage Apy₂, compared to late ore stage arsenopyrite, is relatively enriched in As, whereas the later Apy₃ has high concentrations of S, Fe, and Sb, which is consistent with element patterns in associated main and late ore stage pyrite generations. Compared with pyrite from other stages, the post-ore stage Py₄ has relatively low concentrations of Fe and S, whereas As remains elevated (2.05～3.20 wt%), which could be interpreted by the substitution of As^? for S in the pyrite structure. These results suggest that syngenetic/diagenetic pyrite is the main metal source for the Yangshan gold deposits where such pyrite was metamorphosed at depth below presently exposed levels. The ore-forming elements were concentrated into the hydrothermal fluids during metamorphic devolatilization, and subsequently, during extensive fluid–rock interaction at shallower levels, these elements were precipitated via widespread sulfidation during the main ore stage.     

A Study of Ore-forming Fluids in the Shimensi Tungsten Deposit, Dahutang Tungsten Polymetallic Ore Field, Jiangxi Province, China

The Dahutang tungsten polymetallic ore field is located north of the Nanling W-Sn polymetallic metallogenic belt and south of the Middle—Lower Yangtze River Valley Cu-Mo-Au-Fe porphyry-skarn belt.It is a newly discovered ore field,and probably represents the largest tungsten mineralization district in the world.The Shimensi deposit is one of the mineral deposits in the Dahutang ore field,and is associated with Yanshanian granites intruding into a Neoproterozoic granodiorite batholith.On the basis of geologic studies,this paper presents new petrographic,microthermometric,laser Raman spectroscopic and hydrogen and oxygen isotopic studies of fluid inclusions from the Shimensi deposit.The results show that there are three types of fluid inclusions in quartz from various mineralization stages:liquid-rich two-phase fluid inclusions,vapor-rich two-phase fluid inclusions,and three-phase fluid inclusions containing a solid crystal,with the vast majority being liquid-rich two-phase fluid inclusions.In addition,melt and melt-fluid inclusions were also found in quartz from pegmatoid bodies in the margin of the Yanshanian intrusion.The homogenization temperatures of liquid-rich two-phase fluid inclusions in quartz range from 162 to 363℃ and salinities are 0.5wt%-9.5wt%NaCI equivalent.From the early to late mineralization stages,with the decreasing of the homogenization temperature,the salinity also shows a decreasing trend.The ore-forming fluids can be approximated by a NaCl-H_2O fluid system,with small amounts of volatile components including CO_2,CH_4 and N_2,as suggested by Laser Raman spectroscopic analyses.The hydrogen and oxygen isotope data show that δ5D_(V-smow) values of bulk fluid inclusions in quartz from various mineralization stages vary from-63.8‰ to-108.4‰,and the δ~(18)O_(H2O) values calculated from the δ~(18)O_(V-)smow values of quartz vary from-2.28‰ to 7.21‰.These H-O isotopic data are interpreted to indicate that the ore-forming fluids are mainly composed of magmatic water in the early stage,and meteoric water was added and participated in mineralization in the late stage.Integrating the geological characteristics and analytical data,we propose that the ore-forming fluids of the Shimensi deposit were mainly derived from Yanshanian granitic magma,the evolution of which resulted in highly differentiated melt,as recorded by melt and melt-fluid inclusions in pegmatoid quartz,and high concentrations of metals in the fluids.Cooling of the ore-forming fluids and mixing with meteoric water may be the key factors that led to mineralization in the Dahutang tungsten polymetallic ore field.     

满洲里地区银铅锌矿床成矿流体特征及矿床成因

满洲里地区是得尔布干成矿带最重要的银铅锌矿床产出地区。文中以额仁陶勒盖银矿床和查干布拉根银铅锌矿床为例,系统研究了该区银铅锌矿床成矿流体特征,探讨了矿床成因类型。研究表明,额仁陶勒盖银矿床以气液两相水溶液包裹体为主,流体包裹体均一温度为242～334℃,平均265℃,盐度(质量分数)为1.73%～4.48%NaCl_(eqv),平均2.70%NaCl_(eqv),流体密度为0.72～0.84 g/cm~3,平均0.80 g/cm~3,流体压力为13～26 MPa,平均18 MPa,对应的成矿深度为0.5～1.0 km,平均0.7 km,成矿流体总体上属于H_2O-NaCl体系。查干布拉根银铅锌矿床发育气液两相水溶液包裹体、含CO_2包裹体和纯CO_2包裹体,流体包裹体均一温度为179～367℃,平均261℃,盐度(质量分数)为2.23%～6.87%NaCl_(eqv),平均4.35%NaCl_(eqv),流体密度为0.65～0.91 g/cm~3,平均0.82 g/cm~3,成矿压力为15～46 MPa,平均25 MPa,对应的成矿深度为0.6～1.7km,平均0.9 km,成矿流体总体上属于H_2O-CO_2-CH_4-NaCl体系。两个矿床的成矿流体均属于中低温、低盐度、中等密度流体。额仁陶勒盖银矿床成矿流体主要来自大气降水,大气水的混入是银沉淀的主要机制,其矿床成因属于浅成低温热液型;查干布拉根银铅锌矿床成矿流体属于岩浆水与大气降水的混合水,流体不混溶作用或沸腾作用是查干布拉根矿床银铅锌沉积的主要机制,其矿床成因属于中低温热液脉型。满洲里地区银铅锌矿床的成矿时代为早白垩世,成矿与晚侏罗世—早白垩世火山-侵入岩浆活动晚期的火山-次火山热液密切相关,矿床产出于伸展背景下的中生代陆相火山断陷盆地中。     

滇东铅锌多金属矿成矿过程探讨

位于扬子陆块南部被动边缘褶-冲带的滇东铅锌多金属成矿区是我国重要的铅锌多金属矿产地之一。区内矿床赋矿围岩为震旦系-二叠系碳酸盐岩,以构造控矿为主;成矿过程漫长,成矿元素来自上下不同层位的地层中,成矿流体具多源特征。本次研究收集了前人关于滇东地区铅锌多金属矿勘查和研究成果,并利用作者在滇东地区长期从事矿产勘查所获得的资料...     

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.     

陕西凤太矿集区典型金矿地质特征及其成矿规律

凤太矿集区金矿资源丰富,近年来金矿勘查取得了较大成果和找矿突破.通过分析对比矿集区内典型金矿的地质特征与成矿流体特征,总结了凤太矿集区的成矿规律.凤太矿集区金矿的矿化类型多样,但其成矿流体的性质和来源、成矿物质的来源具有统一性,成矿深度较浅的金矿流体中大气降水的参与程度较高,而成矿深度较深的金矿流体来源则具有更多的变质...     

新疆南天山阿沙哇义金矿床的成因与找矿启示:来自流体和硫化物成分的限定

阿沙哇义金矿位于中国新疆南天山造山带,属于著名的中亚南天山锑-汞-金成矿带的东延部分。该矿床严格受断裂所控制,以浸染状黄铁矿化、毒砂化为特征。矿化可分为三个阶段:早期无矿或贫矿石英阶段,中期石英多金属硫化物阶段,晚期石英-碳酸盐阶段。其中,中期是主要成矿阶段。成矿流体气相成分以H_2O为主,摩尔含量为75%～93%,其次为CO_2,摩尔含量为6%～25%,其余为CH_4、C_2H_6、H_2S、N_2和Ar;液相成分阳离子以Na~+为主,含少量K~+、Ca~(2+)离子,阴离子以Cl~-为主,SO~(2-)次之;矿石的Au含量与其流体的CO_2含量呈反相关,与K~+含量呈正相关。硫化物成分分析结果表明:(1)围岩地层和矿石中的黄铁矿和毒砂是重要的载金矿物,黄铁矿Au含量为0～0. 09%,平均值0. 03%;毒砂Au含量为0～0. 28%,平均值0. 07%;(2)黄铁矿和毒砂Au含量与其自形程度没有明显的相关性;(3)环带状黄铁矿较均质结构黄铁矿具有更高的Au含量;(4)岩体中的黄铁矿几乎不含Au。在成矿构造环境、成矿流体特征及演化、金矿富集机制、成矿温压条件等方面,该矿床与世界上大多数造山型金矿显示出一致性,成矿类型应属于剥蚀程度较浅的造山型金矿。断层阀作用控制的断层愈合-破裂导致的流体不混溶作用是本区金富集、沉淀的最重要机制,但流体混合机制对金的富集沉淀也发挥了作用。黄铁矿、毒砂发育及较多的含炭物质三者共存是本区寻找富矿的关键标志。     

Fluid Inclusions and Metallization of the Kendekeke Polymetallic Deposit in Qinghai Province,China

The Kendekeke polymetallic deposit, located in the middle part of the magmatic arc belt of Qimantag on the southwestern margin of the Qaidam Basin, is a polygenetic compound deposit in the Qimantag metallogenic belt of Qinghai Province. Multi-periodic ore-forming processes occurred in this deposit, including early-stage iron mineralization and lead-zinc-gold-polymetallic mineralization which was controlled by later hydrothermal process. The characteristics of the ore-forming fluids and mineralization were discussed by using the fluid inclusion petrography, Laser Raman Spectrum and micro-thermometry methods. Three stages, namely, S1-stage(copper-iron-sulfide stage), S2-stage(lead-zinc-sulfide stage) and C-stage(carbonate stage) were included in the hydrothermal process as indicated by the results of this study. The fluid inclusions are in three types: aqueous inclusion(type I), CO2-aqueous inclusion(type II) and pure CO2 inclusion(type III). Type I inclusions were observed in the S1-stage, having homogenization temperature at 240–320oC, and salinities ranging from 19.8% to 25.0%(wt % NaCl equiv.). All three types of inclusions, existing as immiscible inclusion assemblages, were presented in the S2-stage, with the lowest homogenization temperature ranging from 175 oC to 295oC, which represents the metallogenic temperature of the S2-stage. The salinities of these inclusions are in the range of 1.5% to 16%. The fluid inclusions in the C-stage belong to types I, II and III, having homogenization temperatures at 120–210oC, and salinities ranging from 0.9% to 14.5%. These observations indicate that the ore-forming fluids evolved from high-temperature to lowtemperature, from high-salinity to low-salinity, from homogenization to immiscible separation. Results of Laser Raman Spectroscopy show that high density of CO2 and CH4 were found as gas compositions in the inclusions. CO2, worked as the pH buffer of ore-forming fluids, together with reduction of organic gases(i.e. CH4, etc), affected the transport and sediment of the minerals. The fluid system alternated between open and close systems, namely, between lithostatic pressure and hydrostatic pressure systems. The calculated metallogenic pressures are in the range of 30 to 87 Mpa corresponding to 3 km mineralization depth. Under the influence of tectonic movements, immiscible separation occurred in the original ore-forming fluids, which were derived from the previous highsalinity, high-temperature magmatic fluids. The separation of CO2 changed the physicochemical properties and composition of the original fluids, and then diluted by mixing with extraneous fluids such as meteoric water and groundwater, and metallogenic materials in the fluids such as lead, zinc and gold were precipitated.     

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.     

Thermodynamic study of the association and separation of copper and gold in the Shizishan ore field, Tongling, Anhui Province, China

The Shizishan ore field is the largest gold–copper ore field in the Tongling ore district of Anhui Province, China. Copper and gold deposits in the district are present as one-commodity deposits or as deposits with both commodities. Copper and gold mineralization are either cogenetic or are temporally and spatially distinct. We present the results of systematic geochemical analysis of fluid inclusions from typical Au–Cu deposits in the Shizishan ore field; these data are used to determine the solubility of Cu and Au in the ore-forming fluids and to ascertain the mechanisms and factors that controlled variations in the association and separation of copper and gold mineralization. Our results indicate that copper in the ore-forming fluids was transported as CuCl₂⁻ and CuCl⁰ complexes and that the solubility of copper was controlled by variations in Cl⁻ concentration. In addition, the precipitation of copper was controlled by changes in temperature, pH, fO₂, and fO₂. In comparison, gold in the ore-forming fluids was transported as Au(HS)₂⁻ and Au₂S(HS)₂²⁻ complexes, and the solubility of gold was controlled by variations in total sulfur concentration; the precipitation of gold was controlled by temperature, pH, fO₂, and fO₂. These differences between the two elements meant that copper and gold in the ore-forming fluids responded in different ways to changes in physicochemical conditions. Copper precipitated under relatively acidic conditions at high temperatures, while gold precipitated under weakly alkaline conditions at relatively low temperatures; this dissociation resulted in the temporal and spatial separation and zonation of copper and gold mineralization in the Shizishan ore field.     

中甸普朗还原性斑岩型铜矿床：矿物组合与流体组成约束

成矿流体高氧逸度是斑岩铜矿床模式的一个基本原则。虽然亚洲单个矿体储量最大的普朗铜矿床的成矿母岩——普朗复式岩体具氧化性岩浆特点,但其矿物组合及流体成分却与还原性斑岩型铜金矿床一致:矿石中以发育大量磁黄铁矿为特征,构成黄铜矿-磁黄铁矿-黄铁矿为主的矿物组合,不发育表征高氧逸度的原生磁铁矿和硫酸盐(硬石膏等)矿物;成矿流体中含较多CO₂、CO和CH₄等还原性组分,氧逸度低于铁橄榄石-磁铁矿-石英缓冲剂。成矿流体中还原性组分可能来源于普朗复式岩体周围的含碳质千枚岩或深部铁镁质岩浆。还原性流体中铜元素的溶解度比氧化性流体中的低,但金元素的溶解度不受氧化还原条件的影响;而CH₄可使SO₂还原形成S^2-,为辉钼矿的形成提供物质基础;可能是导致普朗铜矿床Cu品位偏低而伴生大量Au、Mo矿化的主要原因之一。普朗铜矿床还原性特征的厘定有益于深入研究其矿床成因、乃至区域斑岩型铜矿床成矿机制。     

中亚地区南天山大型金矿带的地质特征、成矿模型和勘查准则

概要介绍了中亚南天山大型金矿带的构造环境、地质特征和分布特点。中亚南天山是世界重要的金成矿带,其中发育有一系列世界级矿床。在该带中,除了剪切带型(造山型)金矿外,还有夕卡岩型、细网脉型以及爆破角砾岩型。成矿围岩是前寒武纪和早古生代浅变质岩系,成矿与二叠纪花岗质岩石密切相关,成矿流体以富CO2为特征,与矿化有关的围岩蚀变强烈发育,通常以Au,Ag,Sb,Te,As,W和Bi元素组合为地球化学找矿标志。     

Microthermometric measurement of fluid inclusions and its constraints on genesis of PGE-polymetallic deposits in Lower Cambrian black rock series, southern China

Systematic microthermometric measurements of fluid inclusions in the PGE-polymetallic deposits hosted in the Lower Cambrian black rock series in southern China were performed, and the results suggest: (1) there exist two types of fluid inclusions. TypeⅠis of NaCl-H2O system with low-medium salinity, and its homogenization temperatures (Th) and salinities are 106.9- 286.4℃ and ( 0.8- 21.8) wt%NaCl eq. respectively; TypeⅡ is of CaCl2-NaCl-H2O system with medium-high salinities, and its homogenization temperatures and salinities range from 120.1℃ to 269.6℃ and ( 11.4- 31.4) wt%NaCl eq., respectively. The typeⅡ fluid inclusions have been discovered for the first time in this kind of deposits; (2) two generations of ore-forming fluids were recognized. Characteristics of fluid inclusions in the PGE-polymetallic ores and carbonate-quartz stockworks in the underlying phosphorites are almost of no difference, they may represent ore-forming fluids at the main metallogenic stage. The peak value of homogenization temperature of those fluid inclusions is about 170℃, while their salinities possess a remarkable bimodal distribution pattern with two peak values of (27-31) wt%NaCl eq. and (4-6) wt%NaCl eq. On the contrary, fluid inclusions in the carbonate-quartz veins in the hanging wall may represent ore-forming fluids at the post-metallogenetic stage. The homogenization temperatures and the peak values of salinities are mostly 130-170℃ and (12-14) wt%NaCl eq., respectively; (3) nobel gas isotopic composition analyses in combination with the microthermometric measurements of fluid inclusions suggest that the ore-forming fluids at the main metallogenetic stage were probably derived from mixing of basinal hot brines with the CaCl2-NaCl-H2O system and seawater with the NaCl-H2O system; (4) in the Early Cambrian, the basinal hot brines were trapped in the Caledonian basins, which were distributed along the southern margin of the Yangtze Craton, and where giant thick sediments were accumulated, and expelled and migrated laterally along the strata because of the pressure caused by overlying sediments. The basinal hot brines absorbed Ni, Mo, V, PGE from the surrounding rocks and were transformed into ore-bearing hydrothermal fluids with the CaCl2-NaCl-H2O system and medium-high salinities, then ascended along faults and mixed with seawater of the NaCl-H2O system, and finally PGE-polymetallic deposits or occurrences were formed in the black rock series.     

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.