The nature of fluids during pegmatite development in metamorphic terrains: Evidence from Hamadan complex,Sanandaj-Sirjan metamorphic zone,Iran

In the Sanandaj-Sirjan zone of metamorphic belt of Iran, the area south of Hamadan city comprises of metamorphic rocks, granitic batholith with pegmatites and quartz veins. Alvand batholith is emplaced into metasediments of early Mesozoic age. Fluid inclusions have been studied using microthermometry to evaluate the source of fluids from which quartz veins and pegmatites formed to investigate the possible relation between host rocks of pegmatites and the fluid inclusion types. Host minerals of fluid inclusions in pegmatites are quartz, andalusite and tourmaline. Fluid inclusions can be classified into four types. Type 1 inclusions are high salinity aqueous fluids (NaCl_eq >12 wt%). Type 2 inclusions are low to moderate salinity (NaCl_eq <12 wt%) aqueous fluids. Type 3 and 4 inclusions are carbonic and mixed CO₂-H₂O fluid inclusions. The distribution of fluid inclusions indicate that type 1 and type 2 inclusions are present in the pegmatites and quartz veins respectively in the Alvand batholith. This would imply that aqueous magmatic fluids with no detectable CO₂ were present during the crystallization of these pegmatites and quartz veins. Types 3 and 4 inclusions are common in quartz veins and pegmatites in metamorphic rocks and are more abundant in the hornfelses. The distribution of the different types of fluid inclusions suggests that CO₂ fluids generated during metamorphism and metamorphic fluids might also contribute to the formation of quartz veins and pegmatites in metamorphic terrains.     

Fluid inclusions in high-grade gneisses of the Kapuskasing structural zone,Ontario: metamorphic fluids and uplift/erosion path

Fluid inclusions in quartz grains from five samples of high-grade rocks (two paragneisses, an amphibolite, a mafic gneiss and a tonalite dike) from the 2.7 Ga Kapuskasing structural zone (KSZ), Ontario, were examined with petrographic, microthermometric and laser Raman techniques. Three types of fluid inclusions were observed: CO₂-rich, H₂O-rich and mixed CO₂-H₂O. CO₂-rich fluid inclusions are pseudosecondary or secondary in nature and are generally pure CO₂; a few contain varying amounts of CH₄·H₂O-rich fluid inclusions are secondary in nature, contain variable amounts of dissolved salts, and generally contain daughter crystals. Mixed CO₂-H₂O fluid inclusions occur where trails of H₂O-rich inclusions intersect trails of CO₂-rich inclusions. Isochores for high density (p=1.03 g/cm³) pseudosecondary, pure CO₂ inclusions intersect the lower pressure portion of the estimated P-T field for high-grade metamorphism, implying that pure CO₂ was the peak metamorphic fluid. The variable CH₄ content of CO₂ inclusions within graphite-bearing samples suggests that CH₄ was introduced locally after the formation of the CO₂ inclusions; however the origin of the CH₄ remains problematic. An aqueous fluid clearly penetrated the gneisses after the peak metamorphism (during uplift/erosion), forming secondary inclusions and contributing to the minor retrogressive hydration observed in these rocks. The presence of the pseudosecondary, high-density CO₂ inclusions in quartz crystals in the KSZ rocks constrains the uplift/ erosion path for the KSZ to one of simultaneous decrease in pressure and temperature.     

西藏邦布石英脉型金矿床的成因: 流体包裹体及氢-氧同位素证据

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。     

Properties of fluids attending variable recrystallization of quartzite during contact metamorphism in the White‐Inyo Range,California

Fluid inclusions in the metamorphic aureole of the Eureka Valley‐Joshua Flat‐Beer Creek (EJB) pluton in the White‐Inyo Range, California, reveal the compositions and origin of fluids that were present during variable recrystallization of quartzite with sedimentary grain shapes to metaquartzite with granoblastic texture. Metamorphosed sedimentary formations, including quartzites, marbles, calcsilicates and schists, became ductile and strongly attenuated in the aureole during growth of the magma chamber. The microstructures of quartzites have an unusual distribution in that within ~250 m from the pluton, where temperatures exceeded 650 °C, they exhibit relict sedimentary grain shapes, only small amount of grain boundary migration (GBM), and crystallographic preferred orientations (CPOs) dominated by <a> slip. At distances >250 m, quartzites were completely recrystallized by GBM and CPOs are indicative of prism [c] slip, characteristics that are typically associated with H₂O‐assisted, high‐T recrystallization. The lack of extensive GBM in the inner aureole can be attributed to rapid replacement of H₂O by CO₂ produced by reaction of quartz grains with calcite cement that also produced interstitial wollastonite. Fluid inclusions in the inner aureole generally occur in margins of quartz grains and are either wholly aqueous (Type 1) or also contain H₂S, CO₂ and CH₄ (Type 2). Type 2 inclusions occur only in some stratigraphic layers. In both inclusion types, NaCl and CaCl₂, in variable proportions, dominate the solutes in the aqueous phase, whereas FeCl₂ and KCl are less abundant solutes. The solutes indicate attainment of a degree of equilibrium with carbonates and schists that are interbedded with the quartzites. Some Types 1 and 2 inclusions in the inner aureole show evidence of decrepitation due to high amounts of strain and/or heating suffered by the host rocks, which suggests that they represent pore fluids that existed in the rocks prior to contact metamorphism. In addition to Type 1 inclusions, outer aureole quartzites also contain inclusions that contain CO₂ vapour bubbles in addition to aqueous phase (Type 3). These inclusions only occur in interiors of granoblastic quartz that was produced by large amounts of GBM. The aqueous phase has identical ranges of first melting and final ice melting temperatures as Type 1 inclusions, suggesting that they have the same solute compositions. These inclusions are thought to represent the interstitial pore H₂O that promoted recrystallization of quartz and reacted with graphite to produce CO₂. Absence of significant amounts of CH₄ in Type 3 inclusions is attributed to elevated fO₂ that was buffered by mineral assemblages in interbedded schists. As opposed to the large amount of CO₂ that was produced by the wollastonite‐forming reaction in the inner aureole to inhibit GBM, the amount of CO₂ produced in the outer aureole by reaction between H₂O and graphite was apparently insufficient to inhibit recrystallization of quartz.     

Metamorphic fluid flow in the northeastern part of the 3.8-3.7 Ga Isua Greenstone Belt (SW Greenland): A re-evalution of fluid inclusion evidence for early Archean seafloor-hydrothermal systems

Fluid inclusions in quartz globules and quartz veins of a 3.8-3.7 Ga old, well-preserved pillow lava breccia in the northeastern Isua Greenstone Belt (IGB) were studied using microthermometry, Raman spectrometry and SEM Cathodoluminescence Imaging. Petrographic study of the different quartz segregations showed that they were affected by variable recrystallization which controlled their fluid inclusion content. The oldest unaltered fluid inclusions found are present in vein crystals that survived dynamic and static recrystallization. These crystals contain a cogenetic, immiscible assemblage of CO₂-rich (+H₂O, +graphite) and brine-rich (+CO₂, +halite, +carbonate) inclusions. The gas-rich inclusions have molar volumes between 44.8 and 47.5 cm³/mol, while the brine inclusions have a salinity of ∼33 eq. wt% NaCl. Modeling equilibrium immiscibility using volumetric and compositional properties of the endmember fluids indicates that fluid unmixing occurred at or near peak-metamorphic conditions of ∼460 °C and ∼4 kbar. Carbonate and graphite were precipitated cogenetically from the physically separated endmember fluids and were trapped in fluid inclusions.In most quartz crystals, however, recrystallization obliterated such early fluid inclusion assemblages and left graphite and carbonate as solid inclusions in recrystallized grains. Intragranular fluid inclusion trails in the recrystallized grains of breccia cementing and crosscutting quartz veins have CO₂-rich assemblages, with distinctly different molar volumes (either between 43.7 and 47.5 cm³/mol or between 53.5 and 74.1 cm³/mol), and immiscible, halite-saturated H₂O-CO₂-NaCl(-other salt) inclusions. Later intergranular trails have CH₄-H₂ (X_H2 up to ∼0.3) inclusions of variable density (ranging from 48.0 to >105.3 cm³/mol) and metastable H₂O-NaCl(-other salt?) brines (∼28 eq. wt% NaCl). Finally, the youngest fluid inclusion assemblages are found in non-luminescent secondary quartz and contain low-density CH₄ (molar volume > 105.33 cm³/mol) and low-salinity H₂O-NaCl (0.2-3.7 eq. wt% NaCl). These successive fluid inclusion assemblages record a retrograde P-T evolution close to a geothermal gradient of ∼30 °C/km, but also indicate fluid pressure variations and the introduction of highly reducing fluids at ∼200-300 °C and 0.5-2 kbar. The quartz globules in the pillow fragments only contain sporadic CH₄(+H₂) and brine inclusions, corresponding with the late generations present in the cementing and crosscutting veins. We argue that due to the large extent of static recrystallization in quartz globules in the pillow breccia fragments, only these relatively late fluid inclusions have been preserved, and that they do not represent remnants of an early, seafloor-hydrothermal system as was previously proposed.Modeling the oxidation state of the fluids indicates a rock buffered system at peak-metamorphic conditions, but suggests a change towards fluid-graphite disequilibrium and a logf_H2/f_H2O above the Quartz-Fayalite-Magnetite buffer during retrograde evolution. Most likely, this indicates a control on redox conditions and on fluid speciation by ultramafic rocks in the IGB.Finally, this study shows that microscopic solid graphite in recrystallized metamorphic rocks from Isua can be deposited inorganically from a fluid phase, adding to the complexity of processes that formed reduced carbon in the oldest, well-preserved supracrustal rocks on Earth.     

Fluid inclusion characteristics of mesothermal gold deposits in the Xiaoqinling district, Shaanxi and Henan Provinces, People's Republic of China

Fluid inclusions were studied in quartz samples from early (stage I) gold-poor quartz veins and later (stage II) gold- and sulphide-rich quartz veins from the Wenyu, Dongchuang, Qiangma, and Guijiayu mesothermal gold deposits in the Xiaoqinling district, China. Fluid inclusion petrography, microthermometry, and bulk gas analyses show remarkably consistent fluid composition in all studied deposits. Primary inclusions in quartz samples are dominated by mixed CO₂-H₂O inclusions, which have a wide range in CO₂ content and coexist with lesser primary CO₂-rich and aqueous inclusions. In addition, a few secondary aqueous inclusions are found along late-healed fractures. Microthermometry and bulk gas analyses suggest hydrothermal fluids with typically 15–30 mol% CO₂ in stage I inclusions and 10–20 mol% CO₂ in stage II inclusions. Estimates of fluid salinity decrease from 7.4–9.2 equivalent wt.% NaCl to 5.7–7.4 equivalent wt.% NaCl between stage I and II. Primary aqueous inclusions in both stages show consistent salinity with, but slightly lower Th _total than, their coexistent CO₂-H₂O inclusions. The coexisting CO₂-rich, CO₂-H₂O, and primary aqueous inclusions in both stage I and II quartz are interpreted to have been trapped during unmixing of a homogeneous CO₂-H₂O parent fluid. The homogenisation temperatures of the primary aqueous inclusions give an estimate of trapping temperature of the fluids. Trapping conditions are typically 300–370 °C and 2.2 kbar for stage I fluids and 250–320 °C and 1.6 kbar for stage II fluids. The CO₂-H₂O stage I and II fluids are probably from a magmatic source, most likely devolatilizing Cretaceous Yanshanian granitoids. The study demonstrates that gold is largely deposited as pressures and temperatures fall accompanying fluid immiscibility in stage II veins. Received: 15 May 1997 / Accepted: 10 June 1998     

The P-V̄-T-X-f O2 evolution of H2O-CO2-CH4-bearing fluid in a wolframite vein: Reconstruction from fluid inclusion studies

Aqueous-carbonaceous and later pure aqueous fluid inclusions in quartz from a ferberite (Fe_.95Mn_.05 WO₄) vein within the low-grade metamorphic aureole of the Borne granite (French Massif Central) have been studied by microthermometry and Raman spectrometry. The bulk V?-X properties of the aqueous-carbonaceous inclusions have been derived using the equation of state of Heyenet al. (1982) for the low-temperature CO₂-CH₄ system. A P-T path has been proposed for their trapping using the equations of state of Jacobs and Kerrick (1981a) for the H₂O-CO₂-CH₄ system. Two main episodes were reconstructed for the history of the aqueous-carbonaceous fluid. (1) Primary H₂O-CO₂-CH₄ vapourrich inclusions in quartz indicated the early circulation of a low-density fluid (65 mole% H₂O-34 mole% CO₂-1 mole% CH₄ and traces of N₂: d = 0.35 gcm^?3) at around 550° ± 50°C and 700 ± 100 bar. Fluid cooled approximately isobarically to 450°-400°C and was progressively diluted by H₂O with a concomitant increase in density. The fO₂ of the H₂OCO₂-CH₄ fluid, estimated from the equilibrium CO₂ + 2H₂O CH₄ + 2O₂, first ranged from 10^?22 to 10^?27 bar, close to the Q-F-M buffer. Within analytical errors, these values were consistent with the presence of graphite in equilibrium with the fluid. (2) A drop in PCO₂, and therefore a drop in fO₂, was recorded by the secondary liquid-rich inclusions in quartz. The inclusions, formed at and below 400°C, were composed of H₂O and CH₄ only, and fO₂ at that stage was below that fixed by the graphite-fluid equilibrium. This second episode in the fluid-rock system could be explained by the drop of temperature below the blocking temperature of the graphite-fluid equilibrium. According to this interpretation, the blocking of the graphite-fluid equilibrium occurred at T ≥ 370°C and probably at 400°C on account of the pressure correction. Mass spectrometric data show that ferberite contains H₂O, CO₂ and CH₄ in fluid inclusions, which lie in the gap of the V?-X properties of the aqueouscarbonaceous fluid in quartz. Deposition of ferberite probably occurred at around 400°C, the previously inferred blocking temperature, resulting from either the drop in PCO₂, the drop fO₂ and/or the related pH-increase.It is concluded that the existence of a blocking-temperature for the graphite-fluid chemical equilibrium may be a critical factor for maintaining a stable fluid pressure gradient in geothermal systems occurring under greenschist facies conditions in graphite-bearing rocks.     

Compositional zoning of fluid inclusions in the Archaean Junction gold deposit,Western Australia: A process of fluid ‐ wall‐rock interaction?

The Junction gold deposit, in Western Australia, is an orogenic gold deposit hosted by a differentiated, iron‐rich, tholeiitic dolerite sill. Petrographic, microthermometric and laser Raman microprobe analyses of fluid inclusions from the Junction deposit indicate that three different vein systems formed at three distinct periods of geological time, and host four fluid‐inclusion populations with a wide range of compositions in the H₂O–CO₂–CH₄–NaCl ± CaCl₂ system. Pre‐shearing, pre‐gold, molybdenite‐bearing quartz veins host fluid inclusions that are characterised by relatively consistent phase ratios comprising H₂O–CO₂–CH₄ ± halite. Microthermometry suggests that these veins precipitated when a highly saline, >340°C fluid mixed with a less saline ≥150°C fluid. The syn‐gold mineralisation event is hosted within the Junction shear zone and is associated with extensive quartz‐calcite ± albite ± chlorite ± pyrrhotite veining. Fluid‐inclusion analyses indicate that gold deposition occurred during the unmixing of a 400°C, moderately saline, H₂O–CO₂ ± CH₄ fluid at pressures between 70 MPa and 440 MPa. Post‐gold quartz‐calcite‐biotite‐pyrrhotite veins occupy normal fault sets that slightly offset the Junction shear zone. Fluid inclusions in these veins are predominantly vapour rich, with CO₂?CH₄. Homogenisation temperatures indicate that the post‐gold quartz veins precipitated from a 310 ± 30°C fluid. Finally, late secondary fluid inclusions show that a <200°C, highly saline, H₂O–CaCl₂–NaCl–bearing fluid percolated along microfractures late in the deposit's history, but did not form any notable vein type. Raman spectroscopy supports the microthermometric data and reveals that CH₄–bearing fluid inclusions occur in syn‐gold quartz grains found almost exclusively at the vein margin, whereas CO₂–bearing fluid inclusions occur in quartz grains that are found toward the centre of the veins. The zonation of CO₂:CH₄ ratios, with respect to the location of fluid inclusions within the syn‐gold quartz veins, suggest that the CH₄ did not travel as part of the auriferous fluid. Fluid unmixing and post‐entrapment alteration of the syn‐gold fluid inclusions are known to have occurred, but cannot adequately account for the relatively ordered zonation of CO₂:CH₄ ratios. Instead, the late introduction of a CH₄–rich fluid into the Junction shear zone appears more likely. Alternatively, the process of CO₂ reduction to CH₄ is a viable and plausible explanation that fits the available data. The CH₄–bearing fluid inclusions occur almost exclusively at the margin of the syn‐gold quartz veins within the zone of high‐grade gold mineralisation because this is where all the criteria needed to reduce CO₂ to CH₄ were satisfied in the Junction deposit.     

长岭凹陷深层天然气藏中CO_2及CH_4充注次序的流体包裹体证据

对长岭凹陷深层天然气藏储层——营城组火山岩中发育的流体包裹体进行了详细研究,结果表明在火山岩发育的石英、方解石细网脉中均存在较多的碳质流体包裹体,单个包裹体激光拉曼光谱分析结果表明其主要为CO2及CH4两种类型的碳质包裹体。其中方解石细网脉体中发育有原生及次生CH4包裹体,而含CO2包裹体多以原生包裹体产于石英细网脉中。很多含CO2包裹体的石英细脉中发现了含CH4包裹体的方解石脉体的角砾,这就表明石英细脉形成晚于方解石细脉。营城组火山岩储层中CO2及CH4包裹体的产状特征研究表明,松辽盆地深层天然气藏的形成系火山岩成岩后CO2及CH4等气体不同期次充注的结果,CH4气的充注时间早于CO2气,火山岩中发育的原生孔隙及次生裂隙为上述气体的充注和聚集提供了重要通道。     

Physico-chemical conditions of ore deposition in Malanjkhand copper sulphide deposit

Heating and freezing studies on fluid inclusions in quartz from mineralized quartzfeldspar reef reveal the presence of type A CO₂-H₂O (H₂O>50% by volume), type B CO₂-H₂O (H₂O<50% by volume), type C pure CO₂ and type D pure aqueous inclusions. Types A, B and C are primary and/or psuedo-secondary inclusions while type D are secondary. Types A and B homogenize on heating into different phases at similar temperatures ranging between 307 and 476°C, indicating entrapment from boiling hydrothermal solutions. Type D inclusions homogenize into a liquid phase at temperatures between 88 and 196°C. Boiling of hydrothermal solutions led to the formation of a CO₂-rich phase of low density and salinity that coexisted with another dense and saline aqueous phase with very little CO₂ dissolved in it. Ore and gangue mineral assemblage of primary ores indicate that ore deposition was characterized by logf _{O 2}=?34.4 to ?30.2 atm, logf _{S 2}=?11.6 to ?8.8 atm and pH=4.5 to 6.5.     

Role of fluids in migmatites: CO2-H2O fluid inclusions in leucosomes from the Deep Freeze Range migmatites (Terra Nova Bay, Antarctica)

ABSTRACT The metasedimentary sequence of the Deep Freeze Range (northern Victoria Land, Antarctica) experienced high-T/low-F metamorphism during the Cambro-Ordovician Ross orogeny. The reaction Bt + Sil + Qtz = Grt + Crd + Kfs + melt was responsible for the formation of migmatites. Peak conditions were c. 700–750° C, c. 3.5–5 kbar and x_H2Oc. 0.5). Distribution of fluid inclusions is controlled by host rock type: (1) CO₂-H₂O fluid inclusions occur only in graphite-free leucosomes; (2) CO₂–CH₄± H₂O fluid inclusions are the most common type in leucosomes, and in graphite-bearing mesosomes and gneiss; and (3) CO₂–N₂–CH₄ fluid inclusions are observed only in the gneiss, and subordinately in mesosomes. CO₂–H₂O mixtures (41% CO₂, 58% H₂O, 1% Nad mol.%) are interpreted as remnants of a synmig-matization fluid; their composition and density are compatible P–T–a_H2O conditions of migmatization (c. 750° C, c. 4 kbar, x_H2Oc. 0.5). CO₂-H₂O fluid in graphite-free leucosomes cannot originate via partial melting of graphite-bearing mesosomes in a closed system; this would have produced a mixed CO₂–CH₄ fluid in the leucosomes by a reaction such as Bt + Sil + Qtz + C ± H₂O = Grt + Crd + Kfs + L + CO₂+ CH₄. We conclude that an externally derived oxidizing CO₂-H₂O fluid was present in the middle crust and initiated anatexis. High-density CO₂-rich fluid with traces of CH₄ characterizes the retrograde evolution of these rocks at high temperatures and support isobaric cooling (P–T anticlockwise path). In unmigmatized gneiss, mixed CO₂–N₂–CH₄ fluid yields isochores compatible with peak metamorphic conditions (c. 700–750° C, c. 4–4.5 kbar); they may represent a peak metamorphic fluid that pre-dated the migmatization.     

Easily altered minerals and reequilibrated fluid inclusions provide extensive records of fluid and thermal history: gypsum pseudomorphs of the Tera Group, Tithonian-Berriasian, Cameros Basin

This study reports a complex fluid and thermal history using petrography, electron microprobe, isotopic analysis and fluid inclusions in replacement minerals within gypsum pseudomorphs in Tithonian-Berriasian lacustrine deposits in Northern Spain. Limestones and dolostones, formed in the alkaline lakes, contain lenticularly shaped gypsum pseudomorphs, considered to form in an evaporative lake. The gypsum was replaced by quartz and non-ferroan calcite (Ca-2), which partially replaces the quartz. Quartz contains solid inclusions of a preexisting non-ferroan calcite (Ca-1), anhydrite and celestine. High homogenization temperatures (T _h ) values and inconsistent thermometric behaviour within secondary fluid inclusion assemblages in quartz (147?C351°C) and calcite (108?C352°C) indicate high temperatures after precipitation and entrapment of lower temperature FIAs. Th are in the same range as other reequilibrated fluid inclusions from quartz veins in the same area that are related to Cretaceous hydrothermalism. Gypsum was replaced by anhydrite, likely during early burial. Later, anhydrite was partially replaced by Ca-1 associated with intermediate burial temperatures. Afterward, both anhydrite and Ca-1 were partially replaced by quartz and this by Ca-2. All were affected during higher temperature hydrothermalism and a CO₂-H₂O fluid. Progressive heating and hydrothermal pulses, involving a CO₂-H₂O fluid, produce the reequilibration of the FIAs, which was followed by uplift and cooling.     

四川雪宝顶钨锡铍矿床流体包裹体研究及其意义

四川雪宝顶钨锡铍矿床产于花岗岩体与三叠系地层大理岩的接触带,赋矿石英脉受大理岩中的劈理破碎带控制。绿柱石与白钨矿中的包裹体可分为熔融包裹体、流体熔融包裹体和流体包裹体3类。流体包裹体又可分为H2O包裹体、CO2包裹体和CO2-H2O包裹体,其中,绿柱石中以富含CO2-H2O包裹体为显著特征。加热时,富H2O相CO2-H2O包裹体完全均一至H2O相,富CO2相CO2-H2O包裹体完全均一至CO2相,而二者的完全均一温度和均一压力一致,表明它们是同期捕获的CO2-低盐水不混溶包裹体组合。与绿柱石相比,白钨矿中CO2-H2O包裹体数量明显减少,H2O包裹体数量增多,成矿压力与成矿温度均有所降低。含CO2流体在花岗岩体与大理岩接触带附近发生流体不混溶和相分离,CO2的出溶使成矿流体中pH值升高,f(O2)降低,导致钨的溶解度降低而沉淀,这是形成白钨矿的主要原因。     

Geological characteristics, tectonic setting and preliminary interpretations of the Jilau gold–quartz vein deposit, Tajikistan

The southern Tien Shan metallogenic province of Central Asia hosts a number of important gold resources including the Jilau gold–quartz vein system in western Tajikistan. These deposits were formed at the late stages of continent–continent collision in association with subduction-related magmatism, metamorphism and continental margin deformation attributed to the Central Asian Hercynian Orogeny. Jilau is hosted by a Hercynian syntectonic granitoid intrusive that was emplaced into bituminous dolomite country rocks. Economic mineralisation is associated with a dilational jog within a high-angle, oblique dextral-reverse slip shear zone that was undergoing brittle–ductile deformation. The orebody takes the form of shear-zone subparallel quartz veins and lenses that emanate from a steeply plunging ore shoot of veins and stringers within a silicified and sulphidised granodiorite core. It is thought to have formed by a dynamic process in which fluid flow was governed by a fault-valve mechanism. Numerous cycles of fluid pressure build-up, fault failure, jog dilation, fluid flow, phase separation of low salinity H₂O–CO₂–CH₄(–N₂) fluids, and sealing took place. Gold appears together with scheelite and bismuth minerals predominantly as inclusions in arsenopyrite in quartz veins and altered wall-rock, and is mainly associated with quartz containing fluid inclusions enriched in CH₄. The correlation between high gold grades and high CH₄ concentrations suggests that components of the mineralising fluids were derived from, or passed through, the reducing, carbonaceous rocks in the contact aureole of the intrusive. The occurrence of Au and W in an adjacent Hercynian skarn deposit and in the Jilau orebody, infers that the ore metals in both these systems were ultimately derived from a magmatic source. Received: 15 April 1999 / Accepted: 30 December 1999     

Metamorphism of sulfides and gangue quartz at the Degdekan and Gol’tsovsky gold deposits, Magadan oblast

The Degdekan and Gol’tsovsky gold-quartz deposits are located in the southeastern Yana-Kolyma gold belt. The orebodies occur as quartz veins hosted in metaterrigenous rocks and cut by postmineral basic-intermediate dikes. It was established that metamorphism of sulfides and gangue quartz was restricted to a few centimeters off the dike contact. According to sulfide geothermometers, the metamorphic temperatures close to the contact of dikes attained 700°C at the Degdekan deposit and were no higher than 491°C at the Gol’tsovsky deposit. The formation of the forbidden assemblage of quartz and loellingite and its fine-grained texture indicate that the thermal effect on the Degdekan ore was short-term. The prolonged heating of the ore at the Gol’tsovsky deposit gave rise to the aggradation recrystallization of quartz and the formation of equilibrium sulfide aggregates that show only insignificant differences in composition from the primary phases. The average homogenization temperature of primary and pseudosecondary fluid inclusions is 206 ± 40°C in the unmetamorphosed veins and 257 ± 33°C in the metamorphosed veins. The salinity of fluids in the primary and pseudosecondary inclusions in quartz veins of both types varies from 0.5 to 14.0 wt % NaCl equiv. The melting temperature of liquid CO₂ in the carbon dioxide inclusions, ranging from ?57.0 to ?60.8°C, suggests an admixture of CH₄ and/or N₂. The unmetamorphosed quartz veins were formed at a fluid pressure varying from 0.7 to 1.3 kbar, while quartz veins at the contact with dikes crystallized at a pressure of 0.8–1.5 kbar. The results of gas chromatography showed the presence of CO₂ and H₂O, as well as N₂ and CH₄. The average bulk of volatiles contained in the fluid inclusions in quartz from the metamorphosed veins is 1.5–2 times lower than in the unmetamorphosed veins; this proportion is consistent with the occurrence of decrepitated gas inclusions in the heated quartz.     

Phase equilibria in fluid inclusions from the Khtada Lake metamorphic complex

The Khtada Lake. British Columbia, metamorphic complex consists of high grade amphibolite and metasedimentary units with development of gneiss, migmatite and homogeneous autochthonous plutons. Maximum metamorphic conditions are estimated to have exceeded 5 kbar and 700°C.Fluid inclusions in matrix quartz are highly variable in density and composition, ranging from apparently pure CO₂ (gas or liquid or both at room temperature) through CO₂ + H₂O ± CH₄ mixtures to inclusions which are entirely aqueous. They occur along cracks, in groups without planar features and as isolated inclusions. The latter and some which occur in groups, are interpreted to most nearly approximate, in density and composition, the fluids present during the peak of metamorphism.The density and fluid composition data are derived from direct observations of phase changes between ? 180 and + 380°C and from the application of published experimental data in the system CH₄-CO₂-H₂O-NaCl. The most dense, pure CO₂ inclusions indicate a pressure of entrapment at 5 kbar, if a temperature of 700°C is assumed. This is in close agreement with the minimum P-T estimates from the mineral assemblages. Methane was positively identified in inclusions in graphite-bearing specimens. Salt content is concluded to be about 5–6 wt% NaCl equivalent in the aqueous phase in both aqueous and CO₂ + H₂O inclusions. There is evidence of immiscible separation of CO₂-rich and H₂O-rich fluids at temperatures at least as high as 375°C.     

Thermal metamorphism and H2O-CO2-NaCl immiscibility at Patapedia,Quebec: evidence from fluid inclusions

The methamorphic history of the Patapedia thermal zone, Gaspé, Quebec, is re-evaluated in the light of results obtained from a study of fluid inclusions contained in quartz phenocrysts of felsic dyke rocks. The thermal zone is characterised by calc-silicate bodies that have outwardly telescoping prograde metamorphic isograds and display extensive retrograde metamorphism with associated copper mineralization. Three distinct fluid inclusion types are recognized: a low to moderate salinity, high density aqueous fluid (Type I); a low density CO₂ fluid (Type II); and a high salinity, high density aqueous fluid (Type III). Fluid inclusion Types I and II predominate whereas Type III inclusions form <10% of the fluid inclusion population. All three fluid types are interpreted to have been present during prograde metamorphism. Temperatures and pressures of metamorphism estimated from fluid inclusion microthermometry and isochore calculations are 450°–500° C and 700–1000 bars, respectively. A model is proposed in which the metamorphism at Patapedia was caused by heat transferred from a low to moderate salinity fluid of partly orthomagmatic origin (Type I inclusions). During the early stages, and particularly in the deeper parts of the system, CO₂ produced by metamorphism was completely miscible in the aqueous hydrothermal fluid and locally resulted in high XCO₂ fluids. On cooling and/or migrating to higher levels these latter fluids exsolved high salinity aqueous fluids represented by the Type III inclusions. Most of the metamorphism, however, took place at temperature-pressure conditions consistent with the immiscibility of CO₂ and the hydrothermal fluid and was consequently accompanied by the release of large volumes of CO₂ vapour which is represented by Type II inclusions. The final stage of the history of the Patapedia aureole was marked by retrograde metamorphism and copper mineralization of a calcite-free calc-silicate hornfels in the presence of a low XCO₂ fluid.     

Fluid evolution during burial and Variscan deformation in the Lower Devonian rocks of the High-Ardenne slate belt (Belgium): sources and causes of high-salinity and C–O–H–N fluids

Fluid inclusions in quartz veins of the High-Ardenne slate belt have preserved remnants of prograde and retrograde metamorphic fluids. These fluids were examined by petrography, microthermometry and Raman analysis to define the chemical and spatial evolution of the fluids that circulated through the metamorphic area of the High-Ardenne slate belt. The earliest fluid type was a mixed aqueous/gaseous fluid (H₂O–NaCl–CO₂–(CH₄–N₂)) occurring in growth zones and as isolated fluid inclusions in both the epizonal and anchizonal part of the metamorphic area. In the central part of the metamorphic area (epizone), in addition to this mixed aqueous/gaseous fluid, primary and isolated fluid inclusions are also filled with a purely gaseous fluid (CO₂–N₂–CH₄). During the Variscan orogeny, the chemical composition of gaseous fluids circulating through the Lower Devonian rocks in the epizonal part of the slate belt, evolved from an earlier CO₂–CH₄–N₂ composition to a later composition enriched in N₂. Finally, a late, Variscan aqueous fluid system with a H₂O–NaCl composition migrated through the Lower Devonian rocks. This latest type of fluid can be observed in and outside the epizonal metamorphic part of the High-Ardenne slate belt. The chemical composition of the fluids throughout the metamorphic area, shows a direct correlation with the metamorphic grade of the host rock. In general, the proportion of non-polar species (i.e. CO₂, CH₄, N₂) with respect to water and the proportion of non-polar species other than CO₂ increase with increasing metamorphic grade within the slate belt. In addition to this spatial evolution of the fluids, the temporal evolution of the gaseous fluids is indicative for a gradual maturation due to metamorphism in the central part of the basin. In addition to the maturity of the metamorphic fluids, the salinity of the aqueous fluids also shows a link with the metamorphic grade of the host-rock. For the earliest and latest fluid inclusions in the anchizonal part of the High-Ardenne slate belt the salinity varies respectively between 0 and 3.5 eq.wt% NaCl and between 0 and 2.7 eq.wt% NaCl, while in the epizonal part the salinity varies between 0.6 and 17 eq.wt% NaCl and between 3 and 10.6 eq.wt% for the earliest and latest aqueous fluid inclusions, respectively. Although high salinity fluids are often attributed to the original sedimentary setting, the increasing salinity of the fluids that circulated through the Lower Devonian rocks in the High-Ardenne slate belt can be directly attributed to regional metamorphism. More specifically the salinity of the primary fluid inclusions is related to hydrolysis reactions of Cl-bearing minerals during prograde metamorphism, while the salinity of the secondary fluid inclusions is rather related to hydration reactions during retrograde metamorphism. The temporal and spatial distribution of the fluids in the High-Ardenne slate belt are indicative for a closed fluid flow system present in the Lower Devonian rocks during burial and Variscan deformation, where fluids were in thermal and chemical equilibrium with the host rock. Such a closed fluid flow system is confirmed by stable isotope study of the veins and their adjacent host rock for which uniform δ¹⁸0 values of both the veins and their host rock demonstrate a rock-buffered fluid flow system.     

Fluid inclusions in high-pressure granulites of the Pan-African belt in Tanzania (Uluguru Mts): a record of prograde to retrograde fluid evolution

The high-pressure granulites of the Uluguru Mountains are part of the Pan-African belt of Tanzania, the metamorphic evolution of which is characterized by an anticlockwise P-T path. Mineral assemblages that represent distinct metamorphic stages are selected for fluid inclusion studies in order to deduce the fluid evolution in metapelites and pyroxene granulites from the prograde to the retrograde stage. Fluid inclusion data improve the petrologically derived P-T path and confirm the anticlockwise evolution. Fluid inclusions in quartz enclosed in garnet porphyroblasts in metapelites preserve prograde fluids of CO₂–N₂ composition and later-trapped pure CO₂. During isochoric heating at temperatures near the peak of metamorphism, deformation and recrystallization led to fluid homogenization yielding N₂-poor CO₂ composition in the metapelites. Near-peak CO₂–N₂ fluid inclusions in quartz of metapelites and CO₂ inclusions in garnet-pyroxene granulites are characterized by perfect negative crystal shape. Garnet formed in veins and as coronas around orthopyroxene represent the near-isochoric/isobaric cooling stage which is characterized by high-density CO₂-rich fluid inclusions. Up to 15 mol% N₂ in some primary CO₂ inclusions in corona garnet indicate small-scale fluid heterogeneity during the static garnet growth. The fact that high-density fluid inclusions are preserved, suggests a shallow dP/dT slope of the uplift path. Nevertheless, some fluid inclusions decrepitated or re-equilibrated and low-density CO₂ inclusions were trapped in the garnet-pyroxene granulite while N₂–CH₄ inclusions formed in the metapelites. Different fluid compositions in metapelite and metabasite argue for an internal control of the fluid composition by phase equilibria. In shear zones where the pyroxene granulite was transformed into scapolite-biotite schist, CO₂–N₂ and low-density N₂–CH₄ fluid inclusions indicate several stages of tectonic activity and suggest fluid influx from the nearby metapelites. High- and low-salinity aqueous inclusions observed beside CO₂ inclusions in garnet-pyroxene granulites, in vein quartz and shear zones could be of high-grade origin but are mainly re-equilibrated or re-trapped along healed microfractures during lower-grade stages. Received: 21 May 1997 / Accepted: 6 October 1997     

Role of fluid mixing and wallrock sulfidation in gold mineralization at the Semna mine area,central Eastern Desert of Egypt: Evidence from hydrothermal alteration,fluid inclusions and stable isotope data

The Semna gold deposit is one of several vein-type gold occurrences in the central Eastern Desert of Egypt, where gold-bearing quartz veins are confined to shear zones close to the boundaries of small granitoid stocks. The Semna gold deposit is related to a series of sub-parallel quartz veins along steeply dipping WNW-trending shear zones, which cut through tectonized metagabbro and granodiorite rocks. The orebodies exhibit a complex structure of massive and brecciated quartz consistent with a change of the paleostress field from tensional to simple shear regimes along the pre-existing fault segments. Textural, structural and mineralogical evidence, including open space structures, quartz stockwork and alteration assemblages, constrain on vein development during an active fault system. The ore mineral assemblage includes pyrite, chalcopyrite, subordinate arsenopyrite, galena, sphalerite and gold. Hydrothermal chlorite, carbonate, pyrite, chalcopyrite and kaolinite are dominant in the altered metaggabro; whereas, quartz, sericite, pyrite, kaolinite and alunite characterize the granodiorite rocks in the alteration zones. Mixtures of alunite, vuggy silica and disseminated sulfides occupy the interstitial open spaces, common at fracture intersections. Partial recrystallization has rendered the brecciation and open space textures suggesting that the auriferous quartz veins were formed at moderately shallow depths in the transition zone between mesothermal and epithermal veins.Petrographic and microthermometric studies aided recognition of CO₂-rich, H₂O-rich and mixed H₂O–CO₂ fluid inclusions in the gold-bearing quartz veins. The H₂O–CO₂ inclusions are dominant over the other two types and are characterized by variable vapor: liquid ratios. These inclusions are interpreted as products of partial mixing of two immiscible carbonic and aqueous fluids. The generally light δ³⁴S of pyrite and chalcopyrite may suggest a magmatic source of sulfur. Spread in the final homogenization temperatures and bulk inclusion densities are likely due to trapping under pressure fluctuation through repeated fracture opening and sealing. Conditions of gold deposition are estimated on basis of the fluid inclusions and sulfur isotope data as 226–267 °C and 350–1100 bar, under conditions transitional between mesothermal and epithermal systems.The Semna gold deposit can be attributed to interplay of protracted volcanic activity (Dokhan Volcanics?), fluid mixing, wallrock sulfidation and a structural setting favoring gold deposition. Gold was transported as Au-bisulfide complexes under weak acid conditions concomitant with quartz–sericite–pyrite alteration, and precipitated through a decrease in gold solubility due to fluid cooling, mixing with meteoric waters and variations in pH and fO₂.