Hydrothermal Fluid Sources of the Fengjia Barite–fluorite Deposit in Southeast Sichuan,China: Evidence from Fluid Inclusions and Hydrogen and Oxygen Isotopes

The Fengjia barite–fluorite deposit in southeast Sichuan is a stratabound ore deposit which occurs mainly in Lower Ordovician carbonate rocks. Here we present results from fluid inclusion and oxygen and hydrogen isotope studies to determine the nature and origin of the hydrothermal fluids that generated the deposit. The temperature of the ore‐forming fluid shows a range of 86 to 302 °C. Our detailed microthermometric data show that the temperature during mineralization of the fluorite and barite in the early ore‐forming stage was higher than that during the formation of the calcite in the late ore‐forming stage. The salinity varied substantially from 0.18% to 21.19% NaCl eqv., whereas the density was around 1.00 g/cm³. The fluid composition was mainly H₂O (>91.33%), followed by CO₂, CH₄ and traces of C₂H₆, CO, Ar, and H₂S. The dominant cation was Na⁺ and the dominant anion Cl^‐, followed by Ca²⁺, SO₄^2‐, K⁺, and Mg²⁺, indicating a mid–low‐temperature, mid‐low‐salinity, low‐density NaCl–H₂O system. Our results demonstrate that the temperature decreased during the ore‐forming process and the fluid system changed from a closed reducing environment to an open oxidizing environment. The hydrogen and oxygen isotope data demonstrate that the hydrothermal fluids in the study area had multiple sources, primarily formation water, as well as meteoric water and metamorphic water. Combined with the geological setting and mineralization features we infer that the stratabound barite–fluorite deposits originated from mid–low‐temperature hydrothermal fluids and formed vein filling in the fault zone.     

Fluid Inclusions and Stable Isotopic Characteristics of the Yaoling Tungsten Deposit in South China: Metallogenetic Constraints

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 δD_H2O isotopic compositions of the inclusion fluid ranges from ?66.7 to ?47.8‰, with δ¹⁸O_H2O 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.     

Genesis of the Xuebaoding W–Sn–Be Crystal Deposits in Southwest China: Evidence from Fluid Inclusions,Stable Isotopes and Ore Elements

The Xuebaoding crystal deposit, located in northern Longmenshan, Sichuan Province, China, is well known for producing coarse‐grained crystals of scheelite, beryl, cassiterite, fluorite and other minerals. The orebody occurs between the Pankou and Pukouling granites, and a typical ore vein is divided into three parts: muscovite and beryl within granite (Part I); beryl, cassiterite and muscovite in the host transition from granite to marble (Part II); and the main mineralization part, an assemblage of beryl, cassiterite, scheelite, fluorite, apatite and needle‐like tourmaline within marble (Part III). No evidence of crosscutting or overlapping of these ore veins by others suggests that the orebody was formed by single fluid activity. The contents of Be, W, Sn, Li, Cs, Rb, B, and F in the Pankou and Pukouling granites are similar to those of the granites that host Nanling W–Sn deposits. The calculated isotopic compositions of beryl, scheelite and cassiterite (δD, ?69.3‰ to ?107.2‰ and δ¹⁸O_H2O, 8.2‰ to 15.0‰) indicate that the ore‐forming fluids were mainly composed of magmatic water with minor meteoric water and CO₂ derived from decarbonation of marble. Primary fluid inclusions are CO₂? CH₄+ H₂O ± CO₂ (vapor), with or without clathrates and halites. We estimate the fluid trapping condition at T = 220 to 360°C and P > 0.9 kbar. Fluid inclusions are rich in H₂O, F^‐ and Cl^‐. Evidence for fluid‐phase immiscibility during mineralization includes variable L/V ratios in the inclusions and inclusions containing different phase proportions. Fluid immiscibility may have been induced by the pressure released by extension joints, thereby facilitating the mineralization found in Part III. Based on the geochemical data, geological occurrence, and fluid inclusion studies, we hypothesize that the coarse‐grained crystals were formed by: (i) the high content of ore elements and volatile elements such as F in ore‐forming fluids; (ii) occurrence of fluid immiscibility and Ca‐bearing minerals after wall rock transition from granite to marble making the ore elements deposit completely; (iii) pure host marble as host rock without impure elements such as Fe; and (iv) sufficient space in ore veins to allow growth.     

Fluid inclusion and cathodoluminescence studies on fluorite from the Kerio valley, Kenya

The Kerio valley lies between the Elgeyo escarpment and the Tugen hills which mark the western margin of the Kenya rift valley. The main fluorite deposits are located in the southern part of the valley at Kimwarer, Choff and Kamnaon.Three types of inclusion fillings were identified: Liquid+Vapour, Liquid+Daughter Minerals and Liquid. The L+V type is dominant. Inclusions occur as clusters, trails along the crystal growth zones and as isolated ones. Low salinities, apparently lower than the 5% wt. NaCl equivalent, were established. Homogenization temperatures suggest that fluorite mineralization took place at different stages and at temperatures between 120 and 180 °C. Isolated readings above 180°C may be referring to the original inclusions in limestone. These measurements and the absence of CO₂ in the inclusions, as well as the occurrence of vugs and crustifications with fluorite, suggest that mineralization took place at relatively shallow depths.Emission spectrum lines representing Eu²⁺, Dy³⁺, Tb³⁺ and Sm³⁺ in fluorite were identified. Sm³⁺ was detected only in the pinkish luminescence of veined fluorite, whereas the pinkish zone in banded fluorite contains Tb³⁺. Eu²⁺ which gives the strongest emission lines in the blue part of the visible spectrum, apparently is responsible for the strong blue cathodoluminescence (CL) in fluorite. The dominance of Eu²⁺ peaks further points to the fact that fluorite mineralization in the Kerio valley took place in an environment that was enriched in Lanthanide Rare Earth Elements (LREE). The presence of rare earths and radioactive elements in fluorite points towards their enrichment in the environment of fluorite mineralization. A juvenile origin of mineral forming solutions is proposed.Two generations of fluorite were established: allotriomorphic fluorite, forming the matrix, and the idiomorphic variety, occurring either in barite or in druzes in early fluorite. Barite in turn forms idiomorphic crystals in allotriomorphic fluorite. Relics of calcite occur in both K-feldspars and in early fluorite. Oxides and hydroxides of Fe, Mn, Ti and Al commonly occur in open spaces in fluorite. Of significance is the presence of gold in fluorite. Fluorite mineralization is of hydrothermal origin in the post-Miocene era and was formed as a result of metasomatic replacement of marble and open space fillings.     

Physicomechanical properties of cryptocrystalline fluorite from the Suran deposit, southern Urals

Microhardness (H) and fracture toughness (K _1C) have been studied for the main varieties of shock-resistant cryptocrystalline fluorite, a natural ceramic widespread at the Suran deposit. Suran cryptocrystalline fluorite (SCF) is characterized by high fracture toughness (K _1C), which is 2–5 times higher than K _1C of common fluorite monocrystals. The relationship between K _1C and microhardness H is complex and nonlinear. The SCF varieties from the sellaite-fluorite orebody are distinguished by the highest K _1C = 1.9–2.3 MPa m^1/2, which exceeds K _1C = 0.84 MPa m^1/2 of porcelain-like fluorite from the main fluorite orebody. Qualitative and quantitative variations of structural point defects in the studied samples exert a much stronger effect on microhardness than on fracture toughness, which mainly depends on the size of crystallites, their mutual crystallographic orientation, and the structure of intergranular boundaries, i.e., on the parameters seemingly related to recrystallization and/or twinning of fluorite. In general, the nature of the Suran deposit of fluorite ceramic with unusual physicomechanical properties remains a geological puzzle in many respects.     

The Ribeira fluorite district,southern Brazil

The origin and evolution of different ore deposits grouped in the same district are often complex and may involve inheritance from crustal or mantle geochemical anomalies, remobilization of former ore deposits and a polyphase hydrothermal history. Localized in a Proterozoic basement in the Parana state, the Ribeira fluorite district is such an example composed of three deposit types with distinct geological and geochemical characters. Emplaced at different periods from the late Proterozoic to the Cretaceous, they are roughly aligned along a belt nearly 10 km in width and 50 km in length, the southern boundary of which is a transcurrent fault. Two main ore facies are present: (1) microcrystalline ore (< 0.1 mm grains) and (2) macrocrystalline ore (with a grain size of several millimetres). The former results from the replacement of metalimestones or internal karstic sediments and the latter from microcrystalline ore dissolution and pore precipitation or recrystallization. At least two different groups of source rocks can be proposed for the trapped REE in CaF₂: (1) fluorite samples associated with the Mato Preto carbonatitic rocks display a slightly negative ɛNd compatible with a mantle source and a REE pattern with the higher ΣREE and La/Yb ratio in the district; (2) other fluorites have a strongly negative ɛNd (− 14 to − 20) which indicates a crustal source. That fluorine and REE have the same source is possible in strata-bound and fracture-filling deposits, but is doubtful at Mato Preto, the only economic fluorite deposit associated with carbonatite rocks in Brazil. This occurrence within a Precambrian fluorite belt suggests that remobilization of a former strata-bound deposit was a more significant metallogenic process than magmatic differentiation. Editorial handling: DR     

Study on Composition of Inclusions in Minerals and Simulation Experiment on Hydrothermal Metasomatic Process of the Bayan Obo Iron Deposit

On the basis of the mechanism of formation of mineral inclusions, it may be assumed that a certain relation exists between the compositions of fluid inclusions in various minerals formed at the same stage of hydrothermal activity. In order to study the genetic relationships between different minerals in the Bayan Obo iron deposit, the compositions(K~+, Na~+, Ca~+, Mg~+, F~+, Cl~+, CO_2~(2-), ΣSO_4~(2-) and pH) of inclusions in fluorite(23), hematite(13), magnetite(3), sodium pyroxene(2) and dolomite(5) from the main mine and the eastern mine were determined by using the vacuum decrepitation and leaching methods, and cluster analyses of the data on the compostions were made. The Q-mode cluster analysis indicates that some iron oxide minerals in the deposit are related to dolomite of sedimentary origin, while others are related to fluorite and sodium pyroxene--products of hydrothermal activity. The R-mode cluster analysis shows that the components of the leaching solution may be divided into two groups: one includes CO_2~(2-), Mg~(2+) and H~+(pH), which are obviously associated with dolomite; the other comprises Na~+, K~+, Ca~+, F~+, Cl~+ and SO_4~(2-), which may possibly represent the composition of hydrothermal solutions.The reaction of the Na-F-Cl solution(pH 4.72) with hematite dolomite at 300℃ and 5 × 10~7 Pa and under alternately"static and dynamic" conditions produced large amounts of hematite and fluorite and small amounts of smectite and Na(Fe) silicates, and the hematite-fluorite assemblage accords with the actual geological conditions in the deposit. From a comparison between the compositions of"static" and"dynamic" solution samples, it may be known that the flow reaction facilitates the migration of Fe, F, Ca and other components as well as Na-metasomatism(Na and Si are fixed in a solid phase).The study of the compositions of mineral inclusions and simulation experiments on hydrothermal metasomatism have provided new evidence for the hypothesis of metamorphosed-sedimentary and hydrothermal-remoulding origin of the Bayan Obo deposit, and pointed out emphatically that hydrothermal metasomatism plays an important role in the formation of the mineral deposit, particularly in the main and the east mine.     

FTIR spectroscpy of natural fluorite from Ambadongar, Gujarat

The principal aim of this study is to examine the presence of structural water in the form of a hydrous ion (OH-) in fluorites of Ambadongar, Gujarat. Several recent spectroscopic studies indicate that in addition to molecular water in fluid inclusions of fluorite, structurally bound water may occur as H₂O and OH species in hydrothermal fluorite. To further clarify this effect, a FTIR study has been carried on hydrothermal fluorite samples from Ambadongar. The analysis were carried out at room temperature as well as 250°C on powdered samples of yellow, blue-green, blue and colourless fluorites. FTIR spectroscopic measurements of all the fluorites show a broad absorption band between 3439–3410 cm^?1 corresponding to bond of O-H stretching vibration indicating the presence of structurally bound water in all fluorites. This structural water in variable amount as different hydrous species associated with other impurity may act as an energy absorbent in the crystal and production of colour in fluorites. From field study of fluorite veins the colour was determined as blue and purple, which, are commonly inter layered, followed by white, finally yellow and colourless varieties.     

豫西合峪萤石矿矿集区矿床特征及找矿前景

合峪萤石矿矿集区是河南省萤石矿田相对最集中的地段。近年来,多个地勘单位对周边十多个萤石矿权在进行勘查,共提交CaF2矿物量1000万吨以上。本文从该区萤石矿的成矿地质背景、赋矿岩性特征、成矿构造特征分析入手,详细论述不同方向的构造对萤石矿体的控矿作用。研究认为NW向断裂为区域的主要控矿构造及容矿构造,占区域萤石矿资源量的80%,其次是NE向断裂在马丢矿区形成了规模巨大的萤石矿床,并对萤石矿体沿走向、倾向的赋存特征、矿石质量特征进行论述,指出断裂构造破碎带和合峪花岗岩基的出露区及其内外断裂构造破碎带中硅化、绢英岩化和玉髓化等蚀变特征是找矿的直接标志。通过对比鱼池岭钼矿床的矿床特征,初步总结了萤石矿成矿地质背景,为在该区开展萤石矿找矿指明靶区和方向。     

Nature and genesis of a carbonatite-associated fluorite deposit at Speewah, East Kimberley region, Western Australia

Summary The Speewah fluorite deposit (>2.28Mt at 25.5% CaF₂) is sited adjacent to the crustal-scale Greenvale Fault on the western side of the Halls Creek Orogen, in the East Kimberley region of Western Australia. Host rocks are Palaeoproterozoic sedimentary rocks, dolerite and granophyre, Early Cambrian basalt, and the Yungul carbonatite. The deposit comprises mainly fluorite–quartz veins associated with lesser barite, sulfides and calcite, controlled by NNE–SSW and N–S brittle faults and fractures. Cross-cutting field relationships indicate that the fluorite veins were deposited post Early Cambrian.Fluorite–quartz vein textures, including colloform banding and comb texture, combined with microthermometric data from primary fluid inclusions, indicate that fluorite was deposited by the incremental infill of open-space structures in an epizonal, and probably epithermal, environment (<160°C) from complex, Li–Ca–Mg-rich, highly saline ore-fluids.The Yungul carbonatite and intimately-associated replacement-type fluorite have similar levels of REE enrichment and identical chondrite-normalised HREE patterns. Samarium and neodymium isotopic analyses of the fluorite indicate extreme differentiation of the ¹⁴⁷Sm/¹⁴⁴Nd ratio, from 0.0709 to 0.6918. These Sm–Nd isotopic data correspond to a mineral isochron with an age of 122±24Ma, interpreted to represent the age of fluorite deposition.Based on the potentially magmatic fluid composition, the replacement-type fluorite within the carbonatite, the similar HREE patterns of fluorite and carbonatite, and direct, if imprecise, isotopic dating of the fluorite, which confirms that fluorite mineralization is younger than the Early Cambrian basalts, the Speewah fluorite deposit is interpreted to be genetically related to the Yungul carbonatite. The large fluorite resource cannot have been derived from the exposed, low-volume carbonatite dyke. Rather, it must have been sourced from a larger carbonatite body at depth, whose presence is implied from basement-derived xenocrystic zircons in the Yungul carbonatite.     

Fluid Inclusion and Stable Isotope Studies at Don Sixto,a Precious Metal Low Sulfidation Deposit in Mendoza Province,Argentina

The Don Sixto mining area in Mendoza province, central‐western Argentina, contains an epithermal low sulfidation Au–Ag deposit. It is a small deposit (～4 km²), with a gold resource of 36 t. In Don Sixto, ore minerals are disseminated in the hydrothermal quartz veins and hydrothermally altered volcanic‐pyroclastic rock units of Permian–Triassic age. On the basis of the texture, ore mineral paragenesis and cross cutting relationship of gangue minerals, seven stages of mineralization were recognized and described. The first six stages are characterized by quartz veins with minor amounts of base metal minerals and the last stage is represented by fluorite veins with minimal quantities of base metal minerals; the precious metal mineralization is mainly related to the fourth stage. The hydrothermal veins exhibit mainly massive, crustiform and comb infilling textures; the presence of bladed quartz replacement textures and quartz veins with adularia crystals are indicative of boiling processes in the system. Fluid inclusion and complementary stable isotope studies were performed in quartz, fluorite, and pyrite samples from the vein systems. The microthermometric data were obtained from primary, biphasic (liquid‐vapor) fluid inclusion assemblages in quartz and fluorite. The maximum values for salinity and homogenization temperature (T_h) came from the stage IV where quartz with petrographic evidence of boiling has average values of 4.96 wt% NaCl_equiv. and 286.9°C respectively. The lower values are related to the last stage of mineralization, where the fluid inclusions in fluorite have average salinities of 1.05 wt% NaCl_equiv. and average homogenization temperatures of 173.1°C. The oxygen and sulfur isotopic fractionation was analyzed in quartz and pyrite. The calculated isotopic fractionation for oxygen in the hydrothermal fluid is in the range of δ¹⁸O_H2O = ?6.92 up to ?3.08‰, which indicates dominance of a meteoric source for the water, while sulfur reaches δ³⁴S_H2S = 1.09‰, which could be reflecting a possible magmatic, or even a mixed source.     

The analysis of the volatiles from fluid inclusions in hydrothermal fluorite

Volatiles from primary fluid inclusions in hydrothermal fluorite were studied. The gases released were analysed with a mass spectrometer using an internal standard; water-vapour pressure was measured manometrically.To extract the volatiles, both heating and grinding in vacuum were used. In the thermal treatment, volatiles from other sources besides the inclusions were also found: H₂ and hydrocarbons, as well as additional amounts of H₂O and CO₂. The vacuum grinding, on the other hand, leads to volatile deficiency, especially with respect to H₂O and CO₂, due to retention of these components on the ground material.The study of the dependence of amount of volatiles released upon heating, on the grain size of the mineral fractions, was used as additional information for evaluating the amounts of volatiles coming from a source other than inclusions.The thermal studies were supplemented by decrepitophonic measurements.It is concluded that the volatiles from inclusions are represented practically only by CO₂ and H₂O in a 1:100 molar ratio. Conclusions about the conditions of mineral formation are drawn.     

Geochemical Characteristics and Sources of Ore-forming Fluids of the Mayuan Pb-Zn Deposit, Nanzheng, Shaanxi, China

The Mayuan stratabound Pb-Zn deposit in Nanzheng,Shaanxi Province,is located in the northern margin of the Yangtze Plate,in the southern margin of the Beiba Arch.The orebodies are stratiform and hosted in breciated dolostone of the Sinian Dengying Formation.The ore minerals are primarily sphalerite and galena,and the gangue minerals comprise of dolomite,quartz,barite,calcite and solid bitumen.Fluid inclusions from ore-stage quartz and calcite have homogenization tempreatures from 98 to 337℃ and salinities from 7.7 wt%to 22.2 wt%(NaCl equiv.).The vapor phase of the inclusions is mainly composed of CH_4 with minor CO_2 and H_2S.The δD_(fluid) values of fluid inclusions in quartz and calcite display a range from-68‰ to-113‰(SMOW),and the δ~(18)O_(fluid)values calculated from δ~(18)O_(quartz) and δ~(18)O_(calcite) values range from 4.5‰ to 16.7‰(SMOW).These data suggest that the ore-forming fluids may have been derived from evaporitic sea water that had reacted with organic matter.The δ~(13)C_(CH4) values of CH_4 in fluid inclusions range from-37.2‰ to-21.0‰(PDB),suggesting that the CH_4 in the ore-forming fluids was mainly derived from organic matter.This,together with the abundance of solid bitumen in the ores,suggest that organic matter played an important role in mineralization,and that the thermochemical sulfate reduction(TSR) was the main mechanism of sulfide precipitation.The Mayuan Pb-Zn deposit is a carbonate-hosted epigenetic deposit that may be classified as a Mississippi Valley type(MVT) deposit.     

Thermal and chemical evolution of fluids during fluorite deposition in the Zaghouan province, north-eastern Tunisia

Several F, Pb, Zn and Ba deposits are located in the province of Zaghouan in north-eastern Tunisia. They are hosted in Lower Liassic or Upper Jurassic reef limestones, and the overlying condensed Carixian phosphatic limestones and Campanian marls, respectively. The mineralization occurs in three types of orebodies: stratiform replacement heaps and lenses (Jebel Stah and Hammam Zriba), breccia fillings and dissolution void fillings (Sidi Taya) and lodes (Jebel Oust). More than one generation of fluorite is observed in the stratiform deposits. Microthermometric analyses of the inclusion fluids observed in fluorite and quartz show that the economic concentrations of fluorite have deposited from moderate to highly saline (12–22.5 wt% NaCl equivalents) hydrothermal (110–160 °C) mineralizing fluids at the center (Jebel Stah, Sidi Taya) and to the east of the province (Hammam Zriba). Late remobilizations, observed in the stratiform deposits, are related to the circulation of a warmer (up to 185 °C) but less saline (10 wt% NaCl equivalents) fluid (Jebel Stah) and more saline (12–22 wt% NaCl equivalents) fluid (Hammam Zriba). The highest temperature (up to 250 °C) and salinity (32–34 wt% NaCl equivalents) are observed to the west of the province of Zaghouan (Jebel Oust). Less saline (3–6 wt% NaCl equivalents) and moderately hot to hot fluids (up to 220 ± 20 °C) and rich in gaseous CO₂ invade most of the ore deposits in later stages and give rise to the massive quartz within fractures at Jebel Stah. Chemical analyses of the fluids extracted from the inclusions occuring in fluorite show compositions dominated by the presence of Na⁺, Ca²⁺ and Cl⁻ ionic species and allow the mean temperature of the fluids in the source reservoir to be estimated as 275 ± 25 °C. The circulation of the ore-forming fluids is triggered by a regional tectonic extensional phase which occurs within the post-Jurassic to ante-Miocene time interval. The deposition of the economic concentrations of fluorite resulted from the decrease in pressure and temperature of the hydrothermal brines (Jebel Oust), along with the increase in the dissolved calcium activity (Jebel Stah and Sidi Taya), or a decrease in salinity due to the mixing with a hot, less saline and Na-poor, Ca-rich fluid (Hammam Zriba). The mineralogical associations (CaF₂, PbS, ZnS, BaSO₄) hosted within carbonate rocks, the temperatures and the salinities of the fluids that gave rise to the more important ore deposits (110–160 °C and 12–22.5 wt% NaCl equivalents), their composition (Na, Ca, Cl) and the molar ratios between the major ionic species, as well as the presence of liquid hydrocarbons in the mineralizing fluids, show that the ore deposits of the province of Zaghouan belong to the carbonate-hosted F, Pb, Zn, Ba Mississippi Valley-type deposits. Received: 23 June 1995 / Accepted: 18 November 1996     

湖南省萤石矿成矿地质特征及成矿带划分

萤石矿是湖南省优势矿种,资源丰富,类型齐全,开发历史悠久,找矿潜力巨大。为满足国内外对萤石矿日益增长的消费需求,深入研究湖南省萤石矿的控矿因素和富集规律具有重要的现实意义。介绍了湖南省萤石矿的成矿地质背景、资源特征、控矿因素及矿石类型; 结合实际地质资料, 综合分析湖南省萤石矿的成矿分布特征,总结萤石矿的成矿地质特征,划分了矿床成矿系列。研究认为,湖南省萤石找矿,需进一步开展矿产资源潜力评价、矿产资源调查及勘查工作。     

The solubility of fluorite in hydrothermal solutions,an experimental study

The solubility of fluorite in NaCl solutions increases with increasing temperature at all ionic strengths up to about 100°C. Above this temperature, the solubility passes through a maximum and possibly a minimum with increasing temperature at NaCl concentrations of 1.0M or less, and increases continuously with increasing temperature at NaCl concentrations above 1.0M. At any given temperature, the solubility of fluorite increases with increasing salt concentration in NaCl, KCl and CaCl₂ solutions. The solubility follows Debye-Hückel theory for KCl solutions. In NaCl and CaCl₂ solutions, the solubility of fluorite increases more rapidly than predicted by Debye-Hückel theory: the excess solubility is due to the presence of NaF^c, CaF⁺, and possibly of Na₂F⁺. The solubility of fluorite in NaCl-CaCl₂ and in NaCl-CaCl₂-MgCl₂ solutions is controlled by the common ion effect and by the presence of NaF^c, CaF⁺, and MgF⁺. The solubility of fluorite in NaCl-HCl solutions increases rapidly with increasing initial HCl concentration; the large solubility increase is due to the presence of HF^c. It seems likely that complexes other than those identified in this study rarely play a major role in fluoride transport and fluorite deposition at temperatures below 300°C.     

Study on the Physical and Chemical Conditions of Ore Formation of Hetai Ductile Shear Zone—Hosted Gold Deposit and Discovery of Melt Inclusions

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.     

西藏柯月锌多金属矿床地质特征及成矿时代初步研究

柯月锌多金属矿床是北喜马拉雅锑金多金属成矿带上新发现的重要矿床。矿体主要呈脉状、透镜状产于近南北向张扭性断裂中,金属矿物主要有方铅矿、闪锌矿、辉锑矿、脆硫锑铅矿、硫锑铅矿、黄铁矿、毒砂、黄铜矿等,非金属矿物主要有石英、铁锰碳酸盐、方解石等。矿石组构以热液充填交代成因为主。流体包裹体初步研究表明,包裹体以液体包裹体为主,还有少量纯气体和纯液体包裹体。成矿流体为中低温、中低盐度、低密度H2O-Na Cl体系。流体中气液成分以H2O为主,液相中局部含有少量的HCO-3、CO2-3和CO2,气相中局部有少量CO2、CH4、N2。根据含矿石英脉中绢云母40Ar-39Ar定年,准确限定柯月矿床成矿热液活动的时限为21.3 Ma。矿床地质特征表明,柯月为中低温热液脉状锌多金属矿床,是后碰撞造山成矿作用的产物。     

Reconciling fluid inclusion types,fluid processes,and fluid sources in skarns: an example from the Bismark Deposit,Mexico

The Bismark deposit (8.5 Mt at 8% Zn, 0.5% Pb, 0.2% Cu, and 50 g/t Ag) located in northern Mexico is an example of a stock-contact skarn end member of a continuum of deposit types collectively called high-temperature, carbonate-replacement deposits. The deposit is hosted by massive sulfide within altered limestone adjacent to the Bismark quartz monzonite stock (~42 Ma) and the Bismark fault. Alteration concurrently developed in both the intrusion and limestone. The former contains early potassic alteration comprising K-feldspar and biotite, which was overprinted by kaolinite-rich veins and alteration and later quartz, sericite, and pyrite with minor sphalerite and chalcopyrite. Prograde exoskarn alteration in the limestone consists of green andradite and diopside, and transitional skarn comprising red-brown andradite, green hedenbergite and minor vesuvinite, calcite, fluorite, and quartz. The main ore stage post-dates calc-silicate minerals and comprises sphalerite and galena with gangue pyrite, pyrrhotite, calcite, fluorite, and quartz. The entire hydrothermal system developed synchronously with faulting. Fluid inclusion studies reveal several distinct temporal, compositional, and thermal populations in pre-, syn- and post-ore quartz, fluorite, and calcite. The earliest primary fluid inclusions are coexisting vapor-rich (type 2A) and halite-bearing (type 3A; type 3B contain sylvite) brine inclusions (32 to >60 total wt% salts) that occur in pre-ore fluorite. Trapping temperatures are estimated to have been in excess of 400 °C under lithostatic pressures of ~450 bar (~1.5 km depth). Primary fluid inclusions trapped in syn-ore quartz display critical to near critical behavior (type 1C), have moderate salinity (8.4 to 10.9 wt% NaCl equiv.) and homogenization temperatures (Th) ranging from 351 to 438 °C. Liquid-rich type 1A and 1B (calcite-bearing) inclusions occur as primary to secondary inclusions predominantly in fluorite and show a range in Th (104–336 °C) and salinity (2.7–11.8 wt% NaCl equiv.), which at the higher Th and salinity ranges overlap with type 1C inclusions. Oxygen isotope analysis was carried out on garnet, quartz, and calcite (plus carbon isotopes) in pre-, syn-, post-ore, and peripheral veins. Pre-ore skarn related garnets have a δ¹⁸O_mineral range between 3.9 and 8.4‰. Quartz from the main ore stage range between 13.6 and 16.0‰. Calcite from the main ore stage has δ¹³C values of –2.9 to –5.1‰ and δ¹⁸O values of 12.3 to 14.1‰, which are clearly distinct from post-ore veins and peripheral prospects that have much higher δ¹⁸O (16.6–27.3‰) and δ¹³C (1.3–3.1‰) values. Despite the numerous fluid inclusion types, only two fluid sources can be inferred, namely a magmatic fluid and an external fluid that equilibrated with limestone. Furthermore, isotopic data does not indicate any significant mixing between the two fluids, although fluid inclusion data may be interpreted otherwise. Thus, the various fluid types were likely to have formed from varying pressure–temperature conditions through faulting during exsolution of magmatic fluids. Late-stage hydrothermal fluid activity was dominated by the non-magmatic fluids and was post-ore.