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1.
A large number of fluid inclusions are observed in quartz contained in Au ores. A study of the geochemistry of inclusions from the Linglong Au deposit in Shandong Province shows that ore-forming temperature and pressure, frequency of appearance for critical inclusion, and saline halo of the main Au-bearing veins 108 and 51 increase in the direction of Linglong Fault. We concluded accordingly, that: (1) the Linglong Fault was a conduit structure for mineralization and will form a favourable place for prospecting where the fault intersects a host structure trending east-northeast; (2) distinct differences in geochemical characteristics are present in relation to the fluid inclusions contained in Au-bearing quartz veins and barren quartz veins, with the former having higher homogenization temperatures, appearing frequency for critical inclusion, content of CO2, H2 and CH4, and molar concentration ratio of (H2 + CH4) to CO2, than those of the latter; (3) decrepitation curves for the two sorts of quartz veins have obviously different characteristics; and (4) geochemical characteristics of fluid inclusions present in the quartz of quartz-vein-type Au ore deposits demonstrate that its metallogenetic pressure, salinity, and decrepitation temperature all increased progressively towards the deeper part of the quartz vein, approximating those of altered-rock-type Au ore deposits. We already know of some Au mines where quartz-vein-type Au ore deposits are turned at depth into altered-rock-type Au ore deposits. Therefore, attention should be paid to prospecting for altered-rock-type Au ore deposits below the quartz-vein-type. From this study, we believe that the geochemical study of fluid inclusions in minerals is a new and useful exploration approach, which should be further explored and used.  相似文献   

2.
The Xiaojiashan tungsten deposit is located about 200 km northwest of Hami City, the Eastern Tianshan orogenic belt, Xinjiang, northwestern China, and is a quartz vein‐type tungsten deposit. Combined fluid inclusion microthermometry, host rock geochemistry, and H–O isotopic compositions are used to constrain the ore genesis and tectonic setting of the Xiaojiashan tungsten deposit. The orebodies occur in granite intrusions adjacent to the metamorphic crystal tuff, which consists of the second lithological section of the first Sub‐Formation of the Dananhu Formation (D2d 12). Biotite granite is the most widely distributed intrusive bodies in the Xiaojiashan tungsten deposit. Altered diorite and metamorphic crystal tuff are the main surrounding rocks. The granite belongs to peraluminous A‐type granite with high potassic calc‐alkaline series, and all rocks show light Rare Earth Element (REE)‐enriched patterns. The trace element characters suggest that crystallization differentiation might even occur in the diagenetic process. The granite belongs to postcollisional extension granite, and the rocks formed in an extensional tectonic environment, which might result from magma activity in such an extensional tectonic environment. Tungsten‐bearing quartz veins are divided into gray quartz vein and white quartz veins. Based on petrography observation, fluid inclusions in both kinds of vein quartz are mainly aqueous inclusions. Microthermometry shows that gray quartz veins have 143–354°C of Th, and white quartz veins have 154–312°C of Th. The laser‐Raman test shows that CO2 is found in fluid inclusions of the tungsten‐bearing quartz veins. Quadrupole mass spectrometry reveals that fluid inclusions contain major vapor‐phase contents of CO2, H2O. Meanwhile, fluid inclusions contain major liquid‐phase contents of Cl?, Na+. It can be speculated that the ore‐forming fluid of the Xiaojiashan tungsten deposit is characterized by an H2O–CO2, low salinity, and H2O–CO2–NaCl system. The range of hydrogen and oxygen isotope compositions indicated that the ore‐forming fluids of the tungsten deposit were mainly magmatic water. The ore‐forming age of the Xiaojiashan deposit should to be ~227 Ma. During the ore‐forming process, the magmatic water had separated from magmatic intrusions, and the ore‐bearing complex was taken to a portion where tungsten‐bearing ores could be mineralized. The magmatic fluid was mixed by meteoric water in the late stage.  相似文献   

3.
The Aitik Cu–Au–Ag deposit is located in northern Sweden and is hosted by strongly deformed 1.9 Ga Svecofennian volcano-sedimentary rocks. The main copper mineralization, which occurs as disseminations and veinlets, is hosted by garnet–biotite schist. Subeconomic mineralization in the footwall to the ore is hosted by feldspar–biotite–amphibole gneiss and porphyritic quartz monzodiorite. The deposit has been affected by post-mineralization metamorphic and igneous activity. Fluid inclusions in six samples of copper-mineralized quartz veins record the presence of three different fluid populations. The main ore was deposited from an aqueous, highly saline (31–37 eq. wt% NaCl + CaCl2) fluid. This fluid was trapped in inclusions intimately associated with the main chalcopyrite mineralization. Later bornite deposition took place from a less saline (18–27 eq. wt% NaCl + CaCl2), aqueous fluid. A third fluid composed of almost pure CO2, interacted with the copper-rich system during a post-ore event. The Aitik Cu–Au–Ag deposit shares some features with both porphyry-type and Fe-oxide–Cu–Au deposits. A high calcium content of the ore fluids, similar to other Cu–Au deposits in northern Scandinavia, suggests a contribution to the salinity of the mainly magmatic-hydrothermal fluids from evaporitic rocks in stratigraphically lower units.  相似文献   

4.
The Ciemas gold deposit is located in West Java of Indonesia,which is a Cenozoic magmatism belt resulting from the Indo-Australian plate subducting under the Eurasian plate.Two different volcanic rock belts and associated epithermal deposits are distributed in West Java:the younger late Miocene-Pliocene magmatic belt generated the Pliocene-Pleistocene epithermal deposits,while the older late Eocene-early Miocene magmatic belt generated the Miocene epithermal deposits.To constrain the physico-chemical conditions and the origin of the ore fluid in Ciemas,a detailed study of ore petrography,fluid inclusions,laser Raman spectroscopy,oxygen-hydrogen isotopes for quartz was conducted.The results show that hydrothermal pyrite and quartz are widespread,hydrothermal alteration is well developed,and that leaching structures such as vuggy rocks and extension structures such as comb quartz are common.Fluid inclusions in quartz are mainly liquid-rich two phase inclusions,with fluid compositions in the NaCl-H20 fluid system,and contain no or little CO_2.Their homogenization temperatures cluster around 240℃-320℃,the salinities lie in the range of 14-17 wt.%NaCl equiv,and the calculated fluid densities are 0.65-1.00 g/cm~3.The values of δ~(18)O_(H2O-VSMOW)for quartz range from +5.5‰ to +7.7‰,the δD_(VSMOW) of fluid inclusions in quartz ranges from-70‰ to-115‰.All of these data indicate that mixing of magmatic fluid with meteoric water resulted in the formation of the Ciemas deposit.A comparison among gold deposits of West Java suggests that Miocene epithermal ore deposits in the southernmost part of West Java were more affected by magmatic fluids and exhibit a higher degree of sulfldation than those of Pliocene-Pleistocene.  相似文献   

5.
The Dayingezhuang gold deposit, hosted mainly by Late Jurassic granitoids on Jiaodong Peninsula in eastern China, contains an estimated 170 t of gold and is one of the largest deposits within the Zhaoping fracture zone. The orebodies consist of auriferous altered pyrite–sericite–quartz granites that show Jiaojia-type (i.e., disseminated and veinlet) mineralization. Mineralization and alteration are structurally controlled by the NE- to NNE-striking Linglong detachment fault. The mineralization can be divided into four stages: (K-feldspar)–pyrite–sericite–quartz, quartz–gold–pyrite, quartz–gold–polymetallic sulfide, and quartz–carbonate, with the majority of the gold being produced in the second and third stages. Based on a combination of petrography, microthermometry, and laser Raman spectroscopy, three types of fluid inclusion were identified in the vein minerals: NaCl–H2O (A-type), CO2–H2O–NaCl (AC-type), and pure CO2 (PC-type). Quartz crystals in veinlets that formed during the first stage contain mainly AC-type fluid inclusions, with rare PC-type inclusions. These fluid inclusions homogenize at temperatures of 251°C–403°C and have low salinities of 2.2–9.4 wt% NaCl equivalent. Quartz crystals that formed in the second and third stages contain all three types of fluid inclusions, with total homogenization temperatures of 216°C–339°C and salinities of 1.8–13.8 wt% NaCl equivalent for the second stage and homogenization temperatures of 195°C–321°C and salinities of 1.4–13.3 wt% NaCl equivalent for the third stage. In contrast, quartz crystals that formed in the fourth stage contains mainly A-type fluid inclusions, with minor occurrences of AC-type inclusions; these inclusions have homogenization temperatures of 106°C–287°C and salinities of 0.5–7.7 wt% NaCl equivalent. Gold in the ore-forming fluids may have changed from Au(HS)0 as the dominant species under acidic conditions and at relatively high temperatures and fO2 in the early stages, to Au(HS)2– under neutral-pH conditions at lower temperatures and fO2 in the later stages. The precipitation of gold and other metals is inferred to be caused by a combination of fluid immiscibility and water–rock interaction.  相似文献   

6.
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.  相似文献   

7.
西藏邦布石英脉型金矿床是产于印度-亚洲板块陆-陆造山主碰撞汇聚环境下、与大洋俯冲无关的新型造山型金矿床。该矿床位于雅鲁藏布江缝合带南侧朗杰学增生楔的东段南缘,矿体受区域内EW向金地-鲁农复向斜和错古-折木朗壳型脆-韧性剪切带及其次级构造的控制。金矿化主要与石英脉密切相关,并包裹于脉内细粒/粗粒硫化物中。矿区内主要分布有3期石英脉:成矿前钩状石英脉、成矿期石英大脉和成矿后陡立状石英脉。文章对3期石英脉流体包裹体形态、形成温度、密度及H-O同位素等方面进行了详细的对比研究,试图查明成矿流体来源以及金的沉淀机制等问题。研究表明,钩状石英脉内包裹体主要为液相(L)包裹体,成分主要为H2O溶液,其流体可能为早期区域变质的产物;石英大脉内包裹体主要为含CO2气液(VL)两相包裹体,体积较大,成分主要为H2O+CO2+CH4±N2,成矿流体为深源变质流体,并与变质地层中的有机质发生强烈反应;陡立状石英脉内包裹体主要为气液两相包裹体,体积较小,其主要成分为H2O+CO2,流体主要与后期区域变质事件有关,为成矿后变质作用的产物。邦布金矿的主要成矿流体源自深部变质流体,流体不混溶作用可能是导致金矿沉淀的主要原因。  相似文献   

8.
The Hetaoping skarn type Pb–Zn deposit is located in the Baoshan–Narong–Dongzhi block metallogenic belt (BND belt), a belt between the Tengchong terrane and the Lanping basin. The deposit is hosted by marble of the upper Cambrian Hetaoping Formation and there are no outcrops of plutonic rocks present. This deposit is one of two large Pb–Zn deposits recently discovered in the BND belt. The Hetaoping deposit is a high Mn skarn. Four types of fluid inclusions were recognized in quartz from the deposit: vapor-rich inclusions (Type I), liquid-rich inclusions (Type II), pure vapor inclusions (Type III), and pure fluid inclusions (Type IV). The coexistence of Type I and Type III inclusions in Stage I (pre-ore stage) and Stage II (main ore stage) shows evidence of fluid boiling. Quartz-hosted fluid inclusions (Stage I and Stage II) display high homogenization temperatures and salinities (134–315 °C; 3.7–18.6 wt% NaCl equivalent) but calcite-hosted fluid inclusions in Stage III (post-ore stage) record lower homogenization temperatures and salinities (85–214 °C; 0.5–5.4 wt% NaCl equivalent). These data suggest a possible mixing between primary magmatic water and meteoric water. Based on chromatography data, the fluid inclusions in quartz contain abundant CO2 and O2 and subordinate CO, CH4 and C2H2 + C2H4, suggesting an oxidizing environment. Based on their Na/K and Cl/SO4 ratios, fluids contained in fluid inclusions are similar to volcanic spring waters. The low Na/K ratios (0.40–1.34) of the ore-forming fluids may have resulted from interaction with a deep alkaline intermediate-acid intrusion. Hydrogen and oxygen isotope determinations on quartz from different ore stages show low δ18O and δD values relative to VSMOW (−4.3‰ to 2.3‰; −109‰ to −91‰), indicating that the ore-forming fluids were diluted by external fluid sources as the skarn system cooled. Overall, geological and geochemical interpretations suggest that the Hetaoping deposit is a distal manganese skarn Pb–Zn deposit related to concealed intrusions.  相似文献   

9.
THEJINLONGSHANGOLDOREBELTINZHEN’ANCOUN TY,SOUTHERNSHAANXIPROVINCE,ISLOCATEDINTHEWEST ERNQINLINGGOLDPROVINCE(NO.16INFIG.1;CHEN YANJINGETAL.,2004).ITWASDISCOVEREDINTHEDEVO NIANSTRATAINTHELATE1980S).ITSGEOLOGICALSETTING ANDMETALLOGENICEVOLUTIONARESIMILARTOT…  相似文献   

10.
The Campbell-Red Lake gold deposit in the Red Lake greenstone belt, with a total of approximately 840 t of gold (past production + reserves) and an average grade of 21 g/t Au, is one of the largest and richest Archean gold deposits in Canada. Gold mineralization is mainly associated with silicification and arsenopyrite that replace carbonate veins, breccias and wallrock selvages. The carbonate veins and breccias, which are composed of ankerite ± quartz and characterized by crustiform–cockade textures, were formed before and/or in the early stage of penetrative ductile deformation, whereas silicification, arsenopyrite replacement and gold mineralization were coeval with deformation. Microthermometry and laser Raman spectroscopy indicate that fluid inclusions in ankerite and associated quartz (Q1) and main ore-stage quartz (Q2) are predominantly carbonic, composed mainly of CO2, with minor CH4 and N2. Aqueous and aqueous–carbonic inclusions are extremely rare in both ankerite and quartz. H2O was not detected by laser Raman spectroscopic analyses of individual carbonic inclusions and by gas chromatographic analyses of bulk samples of ankerite and main ore-stage quartz (Q2). Fluid inclusions in post-mineralization quartz (Q3) are also mainly carbonic, but proportions of aqueous and aqueous–carbonic inclusions are present. Trace amounts of H2S were detected by laser Raman spectroscopy in some carbonic inclusions in Q2 and Q3, and by gas chromatographic analyses of bulk samples of ankerite and Q2. 3He/4He ratios of bulk fluid inclusions range from 0.008 to 0.016 Ra in samples of arsenopyrite and gold. Homogenization temperatures (T h–CO2) of carbonic inclusions are highly variable (from −4.1 to +30.4°C; mostly to liquid, some to vapor), but the spreads within individual fluid inclusion assemblages (FIAs) are relatively small (within 0.5 to 10.3°C). Carbonic inclusions occur both in FIAs with narrow T h–CO2 ranges and in those with relatively large T h–CO2 variations. The predominance of carbonic fluid inclusions has been previously reported in a few other gold deposits, and its significance for gold metallogeny has been debated. Some authors have proposed that formation of the carbonic fluid inclusions and their predominance is due to post-trapping leakage of water from aqueous–carbonic inclusions (H2O leakage model), whereas others have proposed that they reflect preferential trapping of the CO2-dominated vapor in an immiscible aqueous–carbonic mixture (fluid unmixing model), or represent an unusually H2O-poor, CO2-dominated fluid (single carbonic fluid model). Based on the FIA analysis reported in this study, we argue that although post-trapping modifications and host mineral deformation may have altered the fluid inclusions in varying degrees, these processes were not solely responsible for the formation of the carbonic inclusions. The single carbonic fluid model best explains the extreme rarity of aqueous inclusions but lacks the support of experimental data that might indicate the viability of significant transport of silica and gold in a carbonic fluid. In contrast, the weakness of the unmixing model is that it lacks unequivocal petrographic evidence of phase separation. If the unmixing model were to be applied, the fluid prior to unmixing would have to be much more enriched in carbonic species and poorer in water than in most orogenic gold deposits in order to explain the predominance of carbonic inclusions. The H2O-poor, CO2-dominated fluid may have been the product of high-grade metamorphism or early degassing of magmatic intrusions, or could have resulted from the accumulation of vapor produced by phase separation external to the site of mineralization.Geological Survey of Canada contribution 2004383.  相似文献   

11.
The Yaoling tungsten deposit is a typical wolframite quartz vein‐type tungsten deposit in the South China metallogenic province. The wolframite‐bearing quartz veins mainly occur in Cambrian to Ordovician host rocks or in Mesozoic granitic rocks and are controlled by the west‐north‐west trending extensional faults. The ore mineralization mainly comprises wolframite and variable amounts of molybdenite, chalcopyrite, pyrite, fluorite, and tourmaline. Hydrothermal alteration is well developed at the Yaoling tungsten deposit, including greisenization, silicification, fluoritization, and tourmalinization. Three types of primary/pseudosecondary fluid inclusions have been identified in vein quartz, which is intimately intergrown with wolframite. These include two‐phase liquid‐rich aqueous inclusions (type I), two‐ or three‐phase CO2‐rich inclusions (type II), and type III daughter mineral‐bearing multiphase high‐salinity aqueous inclusions. Microthermometric measurements reveal consistent moderate homogenization temperatures (peak values from 200 to 280°C), and low to high salinities (1.3–39 wt % NaCl equiv.) for the type I, type II, and type III inclusions, where the CO2‐rich type II inclusions display trace amounts of CH4 and N2. The ore‐forming fluids are far more saline than those of other tungsten deposits reported in South China. The estimated maximum trapping pressure of the ore‐forming fluids is about 1230–1760 bar, corresponding to a lithostatic depth of 4.0–5.8 km. The δDH2O isotopic compositions of the inclusion fluid ranges from ?66.7 to ?47.8‰, with δ18OH2O values between 1.63 and 4.17‰, δ13C values of ?6.5–0.8‰, and δ34S values between ?1.98 and 1.92‰, with an average of ?0.07‰. The stable isotope data imply that the ore‐forming fluids of the Yaoling tungsten deposit were mainly derived from crustal magmatic fluids with some involvement of meteoric water. Fluid immiscibility and fluid–rock interaction are thought to have been the main mechanisms for tungsten precipitation at Yaoling.  相似文献   

12.
The Jinman Cu polymetallic deposit is located within Middle Jurassic sandstone and slate units in the Lanping Basin of southwestern China. The Cu mineralization occurs mainly as sulfide‐bearing quartz–carbonate veins in faults and fractures, controlled by a Cenozoic thrust–nappe system. A detailed study of fluid inclusions from the Jinman deposit distinguishes three types of fluid inclusions in syn‐ore quartz and post‐ore calcite: aqueous water (type A), CO2–H2O (type B), and CO2‐dominated (type C) fluid inclusions. The homogenization temperatures of CO2–H2O inclusions vary from 208°C to 329°C, with corresponding salinities from 0.6 to 4.6 wt.% NaCl equivalent. The homogenization temperatures of the aqueous fluid inclusions mainly range from 164°C to 249°C, with salinities from 7.2 to 20.2 wt.% NaCl equivalent. These characteristics of fluid inclusions are significantly different from those of basinal mineralization systems, but similar to those of orogenic or magmatic mineralization systems. The H and O isotope compositions suggest that the ore‐forming fluid is predominantly derived from magmatic water, with the participation of basinal brine. The δ34S values are widely variable between ?9.7 ‰ and 9.7 ‰, with a mode distribution around zero, which may be interpreted by the variation in physico‐chemical conditions or by compositional variation of the sources. The mixing of a deeply sourced CO2‐rich fluid with basinal brine was the key mechanism responsible for the mineralization of the Jinman deposit.  相似文献   

13.
Moreira Gomes is a recently discovered deposit (21.7 t Au) of the Cuiú-Cuiú goldfield, Tapajós Gold Province, Amazonian Craton. The mineralized zone is about 1200 m long, 30–50 m wide, and at least 400 m in depth. The zone is controlled by a subvertical, east–west-trending structure that is related to a left lateral strike-slip fault system. The host rocks are predominantly tonalites of the Creporizão Intrusive Suite (1997 ± 2 Ma) of uncertain tectonic setting (magmatic arc or post-collision). Hydrothermal alteration and mineralization are predominantly of the fissure-filling type and locally pervasive. Sericitization, chloritization, sulfidation, silicification, carbonatization and epidotization are the observed alteration types. Pyrite is the predominant sulfide mineral and bears inclusions of chalcopyrite, galena, sphalerite and minor hessite and bismuthinite. Gold occurs predominantly as inclusions in pyrite and subordinately in the free-milling state in quartz veins. Ag, Pb and Bi have been detected by semi-quantitative EDS analysis.Three types of fluid inclusions, hosted in quartz veins and veinlets, have been identified. (1) one- and two-phase CO2 inclusions; (2) two- and three-phase H2O–CO2-salt inclusions, and (3) two-phase H2O-salt inclusions. The CO2-bearing types are interpreted as the product of phase separation of an immiscible fluid. This fluid presents low to moderate density, low to moderate salinity (1.6–11.8 wt.% NaCl equivalent) and was trapped at 280° to 350 °C. The chemical system of the aqueous inclusions may contain CaCl2 and/or MgCl2, salinity varies from zero to 10.1 wt.% NaCl equivalent. Only locally salinities up to 25% have been recorded. This fluid was trapped between 120° and 220 °C and is interpreted as resulting from mixing of a hotter and more saline aqueous fluid (in part derived from phase separation of the H2O–CO2 fluid) with a cooler and dilute aqueous fluid.The δ34S values of pyrite (−0.3‰ to 3.9‰) are probably related to magmatic sulfur. The isotopic composition of inclusion fluids and of the fluid in equilibrium with hydrothermal minerals (quartz, chlorite, and calcite) show δ18O and δD values that range from +0.5 to +9.8‰, and from −49 to −8‰, respectively. Mineral pairs show equilibrium isotopic temperatures that are compatible with the fluid inclusion homogenization temperatures and with textural relationships of the hydrothermal minerals.Isotopic results combined with mineralogical and fluid inclusion data are interpreted to reflect a magmatic-hydrothermal system that evolved in at least three stages. (1) Exsolution of a CO2-bearing magmatic fluid between 400 °C and 320–350 °C and up to 2.1 kbar (6 km in depth) followed by phase separation and main precipitation of the hydrothermal assemblage composed of chlorite–sericite–pyrite–quartz-gold. (2) Cooling and continuous exsolution of CO2 produced a CO2-depleted and slightly more saline aqueous fluid that was trapped mainly at 250°–280 °C. The predominant hydrothermal assemblage of stage 1 continued to form, but epidote is the main phase at this stage. (3) Mixing of the stage 2 aqueous fluid with a cooler and dilute aqueous fluid of meteoric origin, which was responsible for the main carbonatization phase. The mineralizing fluid was neutral to slightly alkaline and relatively reduced. H2S (and/or HS-) might have been the main sulfur species in the fluid and Au(HS)2- was probably the gold transporting complex. Gold deposition occurred as a consequence of a combination of mechanisms, such as phase separation, mixing and fluid-rock interaction.The Moreira Gomes is a granite-hosted gold deposit that is interpreted to be a product of a magmatic-hydrothermal gold system. The age of ore formation (∼1.86 Ga) is consistent with the final stages of evolution of the widespread high-K, calc-alkaline Parauari Intrusive Suite, although the transitional to predominantly alkaline Maloquinha Intrusive Suite cannot be ruled out. Notwithstanding, the deposit does not show the classic features of (oxidized or reduced) intrusion-related gold deposits of Phanerozoic magmatic arcs.  相似文献   

14.
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.  相似文献   

15.
A granite‐related scheelite deposit has been recently discovered in the Wuyi metallogenic belt of southeast China. The veinlet–disseminated scheelite occurs mainly in the inner and outer contact zones of the porphyritic biotite granite, spatially associated with potassic feldspathization and silicification. Re–Os dating of molybdenite intergrowths with scheelite yield a well‐constrained isochron age of 170.4 ± 1.2 Ma, coeval with the LA–MC–ICP–MS concordant zircon age of porphyritic biotite granite (167.6 ± 2.2 Ma), indicating that the Lunwei W deposit was formed in the Middle Jurassic (~170 Ma). We identify three stages of ore formation (from early to late): (I) the quartz–K‐feldspar–scheelite stage; (II) the quartz–polymetallic sulfide stage; and (III) the quartz–carbonate stage. Based on petrographic observations and microthermometric criteria, the fluid inclusions in the scheelite and quartz are determined to be mainly aqueous two‐phase (liquid‐rich and gas‐rich) fluid inclusions, with minor gas‐pure and CO2‐bearing fluid inclusions. Ore‐forming fluids in the Lunwei W deposit show a successive decrease in temperature and salinity from Stage I to Stage III. The homogenization temperature decreases from an average of 299 °C in Stage I, through 251 °C in Stage II, to 212 °C in Stage III, with a corresponding change in salinity from an average of 5.8 wt.%, through 5.2 wt.%, to 3.4 wt.%. The ore‐forming fluids have intermediate to low temperatures and low salinities, belonging to the H2O–NaCl ± CO2 system. The δ18OH2O values vary from 1.8‰ to 3.3‰, and the δDV‐SMOW values vary from –66‰ to –76‰, suggesting that the ore‐forming fluid was primarily of magmatic water mixed with various amounts of meteoric water. Sulfur isotope compositions of sulfides (δ34S ranging from –1.1‰ to +2.4‰) and Re contents in molybdenite (1.45–19.25 µg/g, mean of 8.97 µg/g) indicate that the ore‐forming materials originated mainly in the crust. The primary mechanism for mineral deposition in the Lunwei W deposit was a decrease in temperature and the mixing of magmatic and meteoric water. The Lunwei deposit can be classified as a porphyry‐type scheelite deposit and is a product of widespread tungsten mineralization in South China. We summarize the geological characteristics of typical W deposits (the Xingluokeng, Shangfang, and Lunwei deposits) in the Wuyi metallogenic belt and suggest that porphyry and skarn scheelite deposits should be considered the principal exploration targets in this area.  相似文献   

16.
The Hetai ductile shear zone-hosted gold deposit occurs in the deep-seated fault mylonite zone of the Sinian-Silurian metamorphic rock series. In this study there have been discovered melt inclusions, fluid-melt inclusions and organic inclusions in ore-bearing quartz veins of the ore deposit and mylonite for the first time. The homogenization temperatures of the various types of inclusions are 160℃, 180 - 350℃, 530℃ and 870℃ for organic inclusions, liquid inclusions, two-phase immiscible liquid inclusions and melt inclusions, respectively. Ore fluid is categorized as the neutral to basic K+ -Ca2+ -Mg2+ -Na+ - SO2- 4-HCO3-Cl- system. The contents of trace gases follow a descending order of H2O＞CO2＞CH4＞(or ＜ ) H2＞CO＞C2H2＞C2I-I6＞O2＞N2.The concentrations of K , Ca2 + ,SO2-4,HCO3-,Cl- H2O and C2H2 in fluid inclusions are related to the contents of gold and the Au/Ag ratios in ores from different levels of the gold deposit. This is significant for deep ore prospecting in the region. Daughter minerals in melt inclusions were analyzed using SEM. Quartz, orthoclase, wollastonite and other silicate minerals were identified. They were formed in different mineral assemblages.This analysis further proves the existence of melt inclusions in ore veins. Sedimentary metamorphic rocks could form silicate melts during metamorphic anatexis and dynamic metamorphism, which possess melt-solution characteristics. Ore formation is related to the multi-stage forming process of silicate melt and fluid.  相似文献   

17.
Several occurrences of gold-bearing quartz veins are situated along the east–northeast-trending Barramiya–Um Salatit ophiolitic belt in the central Eastern Desert of Egypt. In the Barramiya mine, gold mineralization within carbonaceous, listvenized serpentinite and adjacent to post-tectonic granite stocks points toward a significant role of listvenitization in the ore genesis. The mineralization is related to quartz and quartz–carbonate lodes in silicified/carbonatized wallrocks. Ore minerals, disseminated in the quartz veins and adjacent wallrocks are mainly arsenopyrite, pyrite and trace amounts of chalcopyrite, sphalerite, tetrahedrite, pyrrhotite, galena, gersdorffite and gold. Partial to complete replacement of arsenopyrite by pyrite and/or marcasite is common. Other secondary phases include covellite and goethite. Native gold and gold–silver alloy occur as tiny grains along micro-fractures in the quartz veins. However, the bulk mineralization can be attributed to auriferous arsenopyrite and arsenic-bearing pyrite (with hundreds of ppms of refractory Au), as evident by electron microprobe and LA-ICP-MS analyses.The mineralized quartz veins are characterized by abundant carbonic (CO2 ± CH4 ± H2O) and aqueous-carbonic (H2O–NaCl–CO2 ± CH4) inclusions along intragranular trails, whereas aqueous inclusions (H2O–NaCl ± CO2) are common in secondary sites. Based on the fluid inclusions data combined with thermometry of the auriferous arsenopyrite, the pressure–temperature conditions of the Barramiya gold mineralization range from 1.3 to 2.4 kbar at 325–370 °C, consistent with mesothermal conditions. Based on the measured δ34S values of pyrite and arsenopyrite intimately associated with gold, the calculated δ34SΣs values suggest that circulating magmatic, dilute aqueous-carbonic fluids leached gold and isotopically light sulfur from the ophiolitic sequence. As the ore fluids infiltrated into the sheared listvenite rocks, a sharp decrease in the fluid fO2 via interaction with the carbonaceous wallrocks triggered gold deposition in structurally favorable sites.  相似文献   

18.
The Nuri Cu‐W‐Mo deposit is located in the southern subzone of the Cenozoic Gangdese Cu‐Mo metallogenic belt. The intrusive rocks exposed in the Nuri ore district consist of quartz diorite, granodiorite, monzogranite, granite porphyry, quartz diorite porphyrite and granodiorite porphyry, all of which intrude in the Cretaceous strata of the Bima Group. Owing to the intense metasomatism and hydrothermal alteration, carbonate rocks of the Bima Group form stratiform skarn and hornfels. The mineralization at the Nuri deposit is dominated by skarn, quartz vein and porphyry type. Ore minerals are chalcopyrite, pyrite, molybdenite, scheelite, bornite and tetrahedrite, etc. The oxidized orebodies contain malachite and covellite on the surface. The mineralization of the Nuri deposit is divided into skarn stage, retrograde stage, oxide stage, quartz‐polymetallic sulfide stage and quartz‐carbonate stage. Detailed petrographic observation on the fluid inclusions in garnet, scheelite and quartz from the different stages shows that there are four types of primary fluid inclusions: two‐phase aqueous inclusions, daughter mineral‐bearing multiphase inclusions, CO2‐rich inclusions and single‐phase inclusions. The homogenization temperature of the fluid inclusions are 280°C–386°C (skarn stage), 200°C–340°C (oxide stage), 140°C–375°C (quartz‐polymetallic sulfide stage) and 160°C–280°C (quartz‐carbonate stage), showing a temperature decreasing trend from the skarn stage to the quartz‐carbonate stage. The salinity of the corresponding stages are 2.9%–49.7 wt% (NaCl) equiv., 2.1%–7.2 wt% (NaCl) equiv., 2.6%–55.8 wt% (NaCl) equiv. and 1.2%–15.3 wt% (NaCl) equiv., respectively. The analyses of CO2‐rich inclusions suggest that the ore‐forming pressures are 22.1 M Pa–50.4 M Pa, corresponding to the depth of 0.9 km–2.2 km. The Laser Raman spectrum of the inclusions shows the fluid compositions are dominated in H2O, with some CO2 and very little CH4, N2, etc. δD values of garnet are between ?114.4‰ and ?108.7‰ and δ18OH2O between 5.9‰ and 6.7‰; δD of scheelite range from ?103.2‰ to ?101.29‰ and δ18OH2O values between 2.17‰ and 4.09‰; δD of quartz between ?110.2‰ and ?92.5‰ and δ18OH2O between ?3.5‰ and 4.3‰. The results indicate that the fluid came from a deep magmatic hydrothermal system, and the proportion of meteoric water increased during the migration of original fluid. The δ34S values of sulfides, concentrated in a rage between ?0.32‰ to 2.5‰, show that the sulfur has a homogeneous source with characteristics of magmatic sulfur. The characters of fluid inclusions, combined with hydrogen‐oxygen and sulfur isotopes data, show that the ore‐forming fluids of the Nuri deposit formed by a relatively high temperature, high salinity fluid originated from magma, which mixed with low temperature, low salinity meteoric water during the evolution. The fluid flow through wall carbonate rocks resulted in the formation of layered skarn and generated CO2 or other gases. During the reaction, the ore‐forming fluid boiled and produced fractures when the pressure exceeded the overburden pressure. Themeteoric water mixed with the ore‐forming fluid along the fractures. The boiling changed the pressure and temperature, oxygen fugacity, physical and chemical conditions of the whole mineralization system. The escape of CO2 from the fluid by boiling resulted in scheelite precipitation. The fluid mixing and boiling reduced the solubility of metal sulfides and led the precipitation of chalcopyrite, molybdenite, pyrite and other sulfide.  相似文献   

19.
The Antuoling Mo deposit is a major porphyry‐type deposit in the polymetallic metallogenic belt of the northern Taihang Mountains, China. The processes of mineralization in this deposit can be divided into three stages: an early quartz–pyrite stage, a middle quartz–polymetallic sulfide stage, and a late quartz–carbonate stage. Four types of primary fluid inclusions are found in the deposit: two‐phase aqueous inclusions, daughter‐mineral‐bearing multiphase inclusions, CO2–H2O inclusions, and pure CO2 inclusions. From the early to the late ore‐forming stages, the homogenization temperatures of the fluid inclusions are 300 to >500°C, 270–425°C, and 195–330°C, respectively, with salinities of up to 50.2 wt%, 5.3–47.3 wt%, and 2.2–10.4 wt% NaCl equivalent, revealing that the ore‐forming fluids changed from high temperature and high salinity to lower temperature and lower salinity. Moreover, based on the laser Raman spectra, the compositions of the fluid inclusions evolved from the NaCl–CO2–H2O to the NaCl–H2O system. The δ18OH2O and δD values of quartz in the deposit range from +3.9‰ to +7.0‰ and ?117.5‰ to ?134.2‰, respectively, reflecting the δD of local meteoric water after oxygen isotopic exchange with host rocks. The Pb isotope values of the sulfides (208Pb/204Pb, 36.320–37.428; 207Pb/204Pb, 15.210–15.495; 206Pb/204Pb, 16.366–17.822) indicate that the ore‐forming materials originated from a mixed upper mantle–lower crust source.  相似文献   

20.
The Chitudian Zn‐Pb ore deposit, Luanchuan, Henan province, was recently discovered in the southern margin of the North China Craton. The Zn‐Pb orebodies are hosted in the Proterozoic Guandaokou and Luanchuan Groups, occurring as veins in interbedding fracture zones mainly in a WNW‐ and partially in a NS‐direction. The Zn‐Pb ores are characterized by banded, massive, and breccia structures, coarse crystal grains, and a simple mineral composition mainly of galena, sphalerite, pyrite, quartz, dolomite, and calcite. In addition to the vein type orebodies, there are Mo‐ and Zn‐bearing skarn orebodies in the northwest of the Chitudian ore field. Four types of primary fluid inclusions in quartz and calcite were recognized in the Chitudian Zn‐Pb ores, including aqueous, aqueous‐CO2, daughter‐mineral‐bearing aqueous, and daughter‐mineral‐bearing aqueous‐CO2 inclusions, with aqueous inclusion being most common. The homogenization temperatures of the fluid inclusions from the main mineralization stage are from 290°C to 340°C, and the salinities mainly from 3.7 to 14.8 wt% NaCl equivalent. In addition to CO2, CH4 and H2S were detected in the vapor phase and HS‐ in the liquid phase of the fluid inclusions by Laser Raman spectroscopy. The δ34SV‐CDT values of ore sulfides from the Chitudian deposit range from ?0.32‰ to 8.30‰, and show two modal peaks in the histogram, one from 1‰ to 4‰, and the other from 5‰ to 7‰. The former peak is similar to that of porphyry‐type Mo‐W deposits in the area, whereas the latter is relatively close to the sulfur in the strata. The ore sulfur may have been derived from both the magma and the strata. The Pb‐isotopic compositions of the ore minerals from Chitudian, with 206Pb/204Pb from 17.005 to l7.953, 207Pb/204Pb from 15.414 to 15.587, and 208Pb/204Pb from 37.948 to 39.036, are similar to those of Mesozoic porphyries in the Chitudian ore field, suggesting that the ore‐forming metals were mainly derived from the Mesozoic magmatic intrusions. The Chitudian Zn‐Pb deposit is interpreted to be a distal hydrothermal vein‐type deposit, which was genetically related to the proximal, skarn‐type Mo ore deposits in the region.  相似文献   

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