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1.
The calculation of fluid evolution paths during reaction progress is considered for multicomponent systems and the results applied to the ternary system, CO2-H2O-NaCl. Fluid evolution paths are considered for systems in which a CO2-rich phase of lesser density (vapour) is preferentially removed from the system leaving behind a saline aqueous phase (liquid). Such boiling leads to enrichment of the residual aqueous phase in dissolved components and, for certain reaction stoichiometries, to eventual saturation of the fluids in salt components. Distinctive textures, particularly radiating growths of prismatic minerals such as tremolite or diopside, are associated with saline fluid inclusions and solid syngenetic salt inclusions at a number of field localities. The most thoroughly studied of these localities is Campolungo, Switzerland, where metasomatic rocks have developed in association with fractures and veins at 500° C and 2,000 bars of pressure. The petrography of these rocks suggests that fluid phase separation into liquid and vapour has been an important process during metasomatism. Fracture systems with fluids at pressure less than lithostatic may facilitate the loss of the less dense vapour phase to conditions of the amphibolite facies.  相似文献   

2.
The data on the mineral composition and crystallization conditions of magnesian skarn and magnetite ore at contacts of dolerite with rock salt and dolomite in ore-bearing volcanic—tectonic structures of the Angara—Ilim type have been integrated and systematized. Optical microscopy, scanning and transmission electron microscopy, electron microprobe analysis, electron paramagnetic resonance, Raman and IR spectroscopy, and methods of mineralogical thermometry were used for studying minerals and inclusions contained therein. The most diverse products of metasomatic reactions are found in the vicinity of a shallow-seated magma chamber that was formed in Lower Cambrian carbonate and saliferous rocks under a screen of terrigenous sequences. Conformable lodes of spinel-forsterite skarn and calciphyre impregnated with magnesian magnetite replaced dolomite near the central magma conduit and apical portions of igneous bodies. At the postmagmatic stage, the following mineral assemblages were formed at contacts of dolerite with dolomite: (1) spinel + fassaite + forsterite + magnetite (T = 820?740°C), (2) phlogopite + titanite + pargasite + magnetite (T = 600–500°C), And (3) clinochlore + serpentine + pyrrhotite (T = 450°C and lower). Rock salt is transformed at the contact into halitite as an analogue of calciphyre. The specific features of sedimentary, contact-metasomatic, and hydrothermal generations of halite have been established. The primary sedimentary halite contains solid inclusions of sylvite, carnallite, anhydrite, polyhalite, quartz, astrakhanite, and antarcticite; nitrogen, methane, and complex hydrocarbons have been detected in gas inclusions; and the liquid inclusions are largely aqueous, with local hydrocarbon films. The contact-metasomatic halite is distinguished by a fine-grained structure and the occurrence of anhydrous salt phases (CaCl2 · KCl, CaCl2, nMgCl2 · mCaCl2) and high-density gases (CO2, H2S, N2, CH4, etc.) as inclusions. The low-temperature hydrothermal halite, which occurs in skarnified and unaltered silicate rocks and in ore, is characterized by a low salinity of aqueous inclusions and the absence of solid inclusions. The composition and aggregative state of inclusions in halite and forsterite indicate that salt melt-solution as a product of melting and dissolution of salt was the main agent of high-temperature metasomatism. Its total salinity was not lower than 60%. The composition and microstructure of magnetite systematically change in different mineral assemblages. Magnetite is formed as a result of extraction of iron together with silicon and phosphorus from dolerite. The first generation of magnetite is represented by mixed crystals, products of exsolution in the Fe-Mg-Al-Ti-Mn-O system. The Ti content is higher at the contact of dolerite with rock salt, whereas, at the contact with dolomite, magnetite is enriched in Mg. The second generation of magnetite does not contain structural admixtures. The distribution of boron minerals and complex crystal hydrates shows that connate water of sedimentary rocks could have participated in hydrothermal metasomatic processes.  相似文献   

3.
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.  相似文献   

4.
The Proterozoic Pahtohavare Cu-Au deposit is located in the greenstone belt near Kiruna, northern Sweden. The greenstone consists of mafic volcanic rocks with pillow lavas, mafic sills and albitized rocks, including tuffites, black schists and mafic sills, together with carbonates and mineralized zones. Mineralization occurs as impregnations, epigenetic quartz-rich breccias and fracture fillings with pyrite, chalcopyrite, pyrrhotite and gold in a complex tectonic environment. Fluid inclusions indicate an early formation of quartz and pyrite at temperatures initially near 500°C and a pressure of 2–2.4 kbar from a supersaturated aqueous solution of magmatic origin. In addition to halite cubes, daughter minerals of sylvite, calcite, hematite, graphite and two unknown phases are found. The main stage of chalcopyrite and gold deposition is characterized by aqueous fluids of variable salinity (up to 30 eq. wt.% NaCl including CaCl2), at temperatures below 350°C and pressures between 1 and 2 kbar. A minor CO2 phase with some N, accompanies this stage. Gold was transported as a chloride complex which destabilized due to an increase in pH (as a consequence of the CO2 loss) as well as cooling and dilution of the solution. The ore deposition occurred as a result of mixing with a low salinity aqueous solution during tectonic fracturing with pressure fluctuations and CO2 unmixing. Late oxidation of ores was caused by low to moderately saline (3 to 13 eq. wt.% NaCl) low temperature aqueous solutions.  相似文献   

5.
江西德兴斑岩铜钼矿床Q+Py±Cp±Cc脉、(黄铁)绢英岩和Q+Py+Mo±Cp脉中发育大量多相(透明、暗色子矿物)包裹体。本文以详细的显微观察和流体包裹体岩相学观察为基础,利用SEM-EDS(扫描电镜-X射线能谱仪)对多相包裹体内的子矿物进行了系统的鉴定。分析结果表明,Q+Py±Cp±Cc脉石英中发育的透明子矿物包括绢云母、石盐、水氯镁石、白云石、铁氯化物、磷灰石和含稀土元素磷酸盐;暗色子矿物包括赤铁矿、铁氧化物和黄铜矿。(黄铁)绢英岩石英和黄铁矿中透明子矿物包括石盐、(硬)石膏、绢云母、硫酸镁、菱镁矿、六水泻盐和(Fe、Cu、Mg)碳酸盐和硫酸盐,暗色子矿物包括磁铁矿、赤铁矿、金红石和黄铜矿;Q+Py+Mo±Cp脉石英包裹体中发育的子矿物相对较少,透明子矿物包括石盐、菱铁矿和钾长石;暗色矿物为赤铁矿。它们中发育种类繁多的子矿物,表明热液的化学成分非常复杂,多种盐类以及高氧化态子矿物出现指示流体具有高盐度-高氧化态的特征。此外,还鉴别出了黄铜矿、赤铁矿和磁铁矿等金属矿物,这表明热液含有丰富的成矿物质,这些成矿物质随物理化学条件的变化以黄铜矿等金属矿物从热液中沉淀下来,形成了矿床内的主要矿体。结合蚀变矿物组成观察,我们认为Q+Py±Cp±Cc脉、(黄铁)绢英岩和Q+Py+Mo±Cp脉中子矿物组成很可能不代表原始流体的化学成分,因为它们在很大程度上受到了热液蚀变作用的影响,围岩矿物由于水-岩反应被分解,同时释放出Na、Ca、Mg、Fe等元素进入热液,形成了上述种类多样的子矿物。通过流体包裹体岩相学观察发现,(黄铁)绢英岩和中Q+Py+Mo±Cp脉含石盐多相包裹体通常与富气包裹体或者CO2包裹体紧密共生,这表明热液在被捕获前发生了相分离(或沸腾)作用,而这一过程必然会导致富液包裹体盐度的升高,因此不能排除这些高盐包裹体是由中低盐度流体发生相分离而形成的可能性。Q+Py±Cp±Cc脉中发育的稀土子矿物指示成脉流体具有高盐度-低pH-含CO2的特征,而这类子矿物在(黄铁)绢英岩和Q+Py+Mo±Cp脉中不发育的原因可能是CO2与液相发生了相分离作用。  相似文献   

6.
This investigation presents and interprets fluid inclusion data from different lithological units of the Cu skarn deposits at Mazraeh, north of Ahar, Azarbaijan, NW Iran. The results provide an assessment of the P–T conditions and mineral–fluid evolution and suggest new exploration parameters. Five types of inclusions are recognized from quartz and garnet. The temperature of homogenization of Type I inclusions with daughter minerals halite and sylvite ranges from 312° to 470 °C with total salinity of 52 to 63 wt.% NaCl equiv.; Type II and III inclusions with halite have homogenization temperatures of 230° to 520 °C and salinity of 31 to 50 wt.% NaCl equiv. The salinity of Types IV and V biphase (liquid + vapor) inclusions, based on their final ice melting temperature, varies between 10.2 to 20.8 wt.% NaCl equiv. Th vs. salinity plots of inclusions show that the salinity of the fluids correlates positively with temperature. The inclusions formed at low pressure. Changes in the temperature and salinity of the fluids can be reconstructed from the inclusions. Highly saline, high-temperature fluids were most abundant during the main chalcopyrite ore-forming phase in the skarn and mineralized quartz veins. Low-salinity aqueous fluids were abundant in barren veins, in which there is no evidence for early hot high-salinity brine, and might have resulted from late-stage dilution and mixing of hydrothermal fluids with meteoric water. Based on petrographic features and fluid-inclusion data, early-stage magnetite deposition is related to boiling of fluid at temperatures of about 500 °C. At a later stage, boiling at temperatures of around 320° to 400 °C favored the deposition of sulfides and Fe mobility was decreased at these lower temperatures. The following inclusion characteristics may be used as exploration parameters in the Mazraeh area. (i) Presence of high-temperature, salt-bearing inclusions, with Th between 300 and 500 °C; (ii) High-salinity fluid inclusions; and (iii) Inclusions showing evidence of boiling of the fluid. In addition, the presence of magnetite is an important exploration parameter.  相似文献   

7.
The Hujiayu Cu deposit,representative of the "HuBi-type" Cu deposits in the Zhongtiao Mountains district in the southern edge of the North China Craton,is primarily hosted in graphitebearing schists and carbonate rocks.The ore minerals comprise mainly chalcopyrite,with minor sphalerite,siegenite[(Co,Ni)_3S_4],and clausthalite[Pb(S,Se)].The gangue minerals are mainly quartz and dolomite,with minor albite.Four fluid inclusion types were recognized in the chalcopyrite-pyrite-dolomite-quartz veins,including CO_2-rich inclusions(type Ⅰ),low-salinity,liquid-dominated,biphase aqueous inclusions(type Ⅱ),solid-bearing aqueous inclusions(type Ⅲ),and solid-bearing aqueous-carbonic inclusions(type Ⅳ).Type I inclusion can be further divided into two sub-types,i.e.,monophase CO_2 inclusions(type Ⅰa) and biphase CO_2-rich inclusions(with a visible aqueous phase),and type Ⅲ inclusion is divided into a subtype with a halite daughter mineral(type Ⅲa) and a subtype with multiple solids(type Ⅲb).Various fluid inclusion assemblages(FIAs) were identified through petrographic observations,and were classified into four groups.The group-1 FIA,consisting of monophase CO_2 inclusions(type Ⅰa),homogenized into the liquid phase in a large range of temperatures from-1 to 28℃,suggesting post-entrapment modification.The group-2 FIA consists of type Ⅰb,Ⅲb and Ⅳ inclusions,and is interpreted to reflect fluid immiscibility.The group-3 FIA comprises type Ⅱ and Ⅲa inclusions,and the group-4FIA consists of type Ⅱ inclusions with consistent phase ratios.The group-1 and group-2 FIAs are interpreted to be entrapped during mineralization,whereas group-3 and group-4 FIAs probably represent the post-mineralization fluids.The solid CO_2 melting temperatures range from-60.6 to56.6℃ and from-66.0 to-63.4℃ for type Ⅰa and type Ⅳ inclusions,respectively.The homogenization temperatures for type Ⅱ inclusions range from 132 to 170℃ for group-3 FIAs and115 to 219℃ for group-4 FIAs.The halite melting temperatures range from 530 to 562℃ for typeⅢ b and Ⅳ inclusions,whereas those for type Ⅲa inclusions range from 198 to 398℃.Laser Raman and SEM-EDS results show that the gas species in fluid inclusions are mainly CO_2 with minor CH_4,and the solids are dominated by calcite and halite.The calcite in the hosting marble and dolomite in the hydrothermal veins have δ~(13)C_(V-pdb) values of-0.2 to 1.2‰ and-1.2 to-6.3‰,and δ~(18)O_(v-smow) values of 14.0 to 20.8 ‰ and 13.2 to 14.3‰,respectively.The fluid inclusion and carbon-oxygen isotope data suggest that the ore-forming fluids were probably derived from metamorphic fluids,which had reacted with organic matter in sedimentary rocks or graphite and undergone phase separation at 1.4-1.8 kbar and 230-240℃,after peak metamorphism.It is proposed that the Hujiayu Cu deposit consists of two mineralization stages.The early stage mineralization,characterized by disseminated and veinlet copper sulfides,probably took place in an environment similar to sediment-hosted stratiform copper mineralization.Ore minerals formed in this precursor mineralization stage were remobilized and enriched in the late metamorphic hydrothermal stage,leading to the formation of thick quartz-dolomite-sulfides veins.  相似文献   

8.
The origin of secondary calcite-silica minerals in primary and secondary porosity of the host Miocene tuffs at Yucca Mountain has been hotly debated during the last decade. Proponents of a high-level nuclear waste repository beneath Yucca Mountain have interpreted the secondary minerals to have formed from cool, descending meteoric fluids in the vadose zone; critics, citing the presence of two-phase fluid inclusions, argued that the minerals could only have formed in the phreatic zone from ascending hydrothermal fluids. Understanding the origin, temperature, and timing of these minerals is critical in characterizing geologically recent fluid flux at the site, and has significant implications to whether waste should be stored at Yucca Mountain.Petrographic and paragenetic studies of 155 samples collected from the Exploratory Studies Facility (ESF) and repository block cross drift (ECRB) tunnels indicate that heterogeneously distributed calcite with lesser chalcedony, quartz, opal, and fluorite comprise the oldest secondary minerals. These are typically overgrown by intermediate-aged calcite, often exhibiting distinctive bladed habits. The youngest event recorded across the site is the deposition of Mg-enriched (up to ∼1 wt%) and depleted, growth-zoned calcite intergrown with U-enriched opal. The cyclical variation in Mg enrichment and depletion is probably related to climate changes that have occurred during the last few million years. The distribution of secondary minerals is consistent with precipitation in the vadose zone.Fluid inclusion petrography of sections from the 155 samples determined that 96% of the fluid inclusion assemblages (FIAs) contained liquid-only inclusions that formed at ambient temperatures (<35°C). However, 50% of the samples (n = 78) contained relatively rare FIA that contain both liquid-only and liquid plus vapor inclusions (herein termed two-phase FIAs) that formed at temperatures above 35°C. Virtually all of these two-phase FIAs occur in paragenetically old calcite; rare two-phase inclusion assemblages were also observed in early fluorite and quartz, and early-intermediate calcite. Homogenization temperatures (≡ trapping temperatures) across Yucca Mountain are generally 45 to 60°C, but higher temperatures reaching 83°C were recorded in calcite from the north portal and ramp of the ESF. Cooler temperatures of ∼35 to 45°C were recorded in the intensely fractured zone. Multiple populations of two-phase FIAs from lithophysal cavities in the ESF and ECRB cross drift indicate early fluid cooling with time from temperatures >45°C in early calcite, to <35 to 45°C in paragenetically younger calcite. Freezing point depressions range from −0.2 to −1.6°C, indicating trapping of a low salinity fluid. The majority of intermediate calcite and all outermost Mg-enriched calcite contains rare all-liquid inclusions and formed from ambient temperature (<35°C) fluids.Carbon and oxygen isotope data reveal a consistent trend of decreasing δ13C (from 9.5 to −8.5‰) and increasing δ18O (from 5.2 to 22.1‰) values from paragenetically early calcite to Mg-enriched growth-zoned calcite. Depleted δD values (−131 to −90‰) of inclusion fluids from intermediate and the youngest Mg-enriched calcite indicate derivation from surface meteoric fluids. Recalculation of δ18OH2O values of −12 to −10‰ is consistent with derivation from paleometeoric fluids.Results of integrated U-Pb dating (opal and chalcedony) and fluid inclusion microthermometry indicate that two-phase FIAs that trapped fluids of >50°C are older than 6.29 ± 0.30 Ma. Two-phase FIAs in paragenetically later calcite, which formed from fluids of 35 to 45°C, are older than 5.32 ± 0.02 Ma. There is no evidence for trapping of fluids with elevated temperatures during the past 5.32 my. The youngest Mg-enriched calcite intergrown with opal began to precipitate between about 1.9 to 2.9 Ma and has continued to precipitate within the past half million years. The presence of liquid-only inclusions and the consistent occurrence of Mg-enriched calcite and opal as the youngest event indicate a minor, but chemically distinct, ambient temperature (<35°C) fluid flux during the past 2 to 3 my.  相似文献   

9.
Fluid and solid inclusions have been studied in selected samples from a series of spinel-bearing Crdiopside-and Al-augite-series ultramafic (harzburgites, lherzolites, and olivine-clinopyroxene-rich rocks), and gabbroic xenoliths from Hierro, Canary Islands. In these samples several generations of fluid inclusions and ultramafic-and mafic-glass inclusions may be texturally related to different stages of crystal growth. The fluid inclusions consist of pure, or almost pure, CO2. The solid inclusions in the ultramafic xenoliths comprise early inclusions of devitrified ultramafic glass, sulphide inclusions, as well as polyphase inclusions (spinel+clinopyroxene±glass±other silicates) believed to have formed from trapped basaltic melts. Vitreous basaltic glass±CO2±sulphide±silicates are common as secondary inclusions in the ultramafic xenoliths, and as primary inclusions in the gabbroic xenoliths. Microthermometry gives minimum trapping temperatures of 1110° C for the early ultramafic-and mafic-glass inclusions, and a maximum of 1260–1280° C for late inclusions of host basaltic glass. In most samples the CO2 inclusions show a wide range in homogenization temperatures (-40 to +31° C) as a result of decrepitation during ascent. The lowest homogenization temperatures of about-40° C, recorded in some of the smallest CO2 inclusions, indicate a minimum depth of origin of 35 km (12 kbar) for both the Cr-diopside-and Al-augite-series xenoliths. The gabbroic xenoliths originate from a former magma chamber at a depth of 6–12 km.Contribution no. 100 of the Norwegian programme of the International Lithosphere Project  相似文献   

10.
大兴安岭岔路口斑岩钼矿床流体成分及成矿意义   总被引：1，自引：0，他引：1       下载免费PDF全文
岔路口超大型斑岩型钼矿床位于大兴安岭北段,以网脉状和角砾岩型矿化为主.该矿床经历了4个成矿阶段:Ⅰ.石英-钾长石;Ⅱ.石英-辉钼矿;Ⅲ.石英-多金属硫化物;Ⅳ.石英-萤石-方解石.包裹体的岩相学及激光拉曼研究揭示,石英斑晶内的熔体-流体包裹体中熔体成分有更长石和钠长石,为岩浆出溶作用形成;子矿物多相包裹体(S型)中含有钾盐、石盐、赤铁矿和石膏等子矿物,显示出成矿流体为高氧逸度.第Ⅰ成矿阶段包裹体有气液两相(L+V型)、富CO2三相(C型)和含石盐、钾盐、赤铁矿及硬石膏等子矿物的多相(S型)等类型,第Ⅱ成矿阶段除了有L+V型、C型以及含钾盐、石盐、黄铜矿和辉钼矿等子矿物多相(S型)外,还可以见到S型包裹体与气相包裹体(V型)共存;第Ⅲ成矿阶段以L+V型和含方解石的S型包裹体为主;第Ⅳ成矿阶段除见到L+V型包裹体外,还可以见到液相包裹体(L型).显微测温结果显示从早到晚,流体包裹体均一温度从530 ℃变为120 ℃、盐度从66.7% NaCl equiv变为1.2% NaCl equiv,呈现逐渐降低的趋势.群体包裹体成分显示各阶段均含有气相CO2,液相成分中Na+,K+,Ca2+,SO42-,Cl-含量很高,而F-含量极少.成矿流体总体属于富含CO2的高盐度、高氧逸度的NaCl-H2O-CO2体系,在流体演化过程中温度、氧逸度、盐度和CO2含量逐渐降低.温度、盐度、CO2含量逐渐降低及绢云母化影响了矿石沉淀.   相似文献   

11.
Oxygen isotope exchange between minerals during metamorphism can occur in either the presence or the absence of aqueous fluids. Oxygen isotope partitioning among minerals and fluid is governed by both chemical and isotopic equilibria during these processes, which progress by intragranular and intergranular diffusion as well as by surface reactions. We have carried out isotope exchange experiments in two- and three-phase systems, respectively, between calcite and tremolite at high temperatures and pressures. The two-phase system experiments were conducted without fluid either at 1 GPa and 680 °C for 7 days or at 500 MPa and 560 °C for 20 days. Extrapolated equilibrium fractionations between calcite and tremolite are significantly lower than existing empirical estimates and experimental determinations in the presence of small amounts of fluid, but closely match calculated fractionations by means of the increment method for framework oxygen in tremolite. The small fractionations measured in the direct calcite–tremolite exchange experiments are interpreted by different rates of oxygen isotope exchange between hydroxyl oxygen, framework oxygen and calcite during the solid–solid reactions where significant recrystallization occurs. The three-phase system experiments were accomplished in the presence of a large amount of fluid (CO2+H2O) at 500 MPa and 560 °C under conditions of phase equilibrium for 5, 10, 20, 40, 80, 120, 160, and 200 days. The results show that oxygen isotope exchange between minerals and fluid proceeds in two stages: first, through a mechanism of dissolution-recrystallization and very rapidly; second, through a mechanism of diffusion and very slowly. Synthetic calcite shows a greater rate of isotopic exchange with fluid than natural calcite in the first stage. The rate of oxygen diffusion in calcite is approximately equal to or slightly greater than that in tremolite in the second stage. A calculation using available diffusion coefficients for calcite suggests that grain boundary diffusion, rather than volume diffusion, has been the dominant mechanism of oxygen transport between the fluid and the mineral grains in the later stage.Editorial responsibility: T.L. Grove  相似文献   

12.
This study provides evidence for the existence of halite and sylvite solid inclusions in igneous quartz and feldspars, the first to be reported in intrusive rocks, and to partially constrain the physicochemical environment that lets halides crystallize under magmatic conditions.Halite and sylvite solid inclusions were found included in quartz and feldspars from a micrographic–granophyric assemblage in a miarolitic aplite and, rarer, in alkali-feldspar from a miarolitic monzogranite. Monzogranite and aplite represent I-type, K-enriched postcollisional rocks of the Late Cambrian–Early Ordovician Sierra Norte–Ambargasta batholith in the Eastern Sierras Pampeanas. Both granitoids fall among the most evolved felsic rocks of the batholith, with aplite approaching haplogranitic compositions. Halite is far more common than sylvite and the presence and distribution of one or both halides are erratic within the felsic intrusive bodies. Halides occur as small skeletal grains, commonly in cross-shaped aggregates of less than 50 μm. No K or Na was found at the detection limits of EDS in either halite or sylvite respectively. Textural relationships suggest that the alkali-chlorides separated from the melt near the minima along the quartz–feldspar cotectics of PH2O > 160 < 200 MPa in a silica-, and potassium-rich magmatic system at approximately 750–700 °C, prior to the H2O-vapor saturated miarole-forming stage.Computed ratios for the magmatic volatile phase (MVP) coexisting with melt at the early stage of aplite crystallization are: NaCl/HCl = 0.11–0.97 and KCl/HCl = 0.24–1.62, being the highest range of values (0.79–0.97 and 1.45–1.62, respectively) found in those alkali-chloride-bearing samples. Maximum HCl/ΣCl(MVP) (0.28 to 0.31) indicates higher total Cl concentration in the MVP of alkali-chloride-bearing aplites, which is much higher in the halite-free aplite samples (HCl/ΣCl(MVP) = 0.59 to 0.74). One miarolitic monzogranite sample, where halite solid inclusions are present, also yielded the highest ratios for NaCl/HCl(MVP) (0.91) and KCl/HCl(MVP) (1.46), and the HCl/ΣCl(MVP) is 0.30. A high HCl concentration in the fluid phase is suggested by the log f(HF)/f(H2O) = − 4.75 to − 4.95, log f(HCl)/f(H2O) = − 3.73 to − 3.86, and log f(HF)/f(HCl) = − 0.88 to − 1.22, computed at 750 °C after biotite composition. The Cl concentrations at 800 °C, computed with a Dv/lCl = 0.84 + 26.6P (P at 200 MPa), yielded values within the range of  70 to 700 ppm Cl in the melt and  4000 to 40 000 ppm Cl in the coexisting MVP. The preferential partitioning of Cl in the vapor phase is controlled by the Dv/lCl; however, the low concentration of Cl in the melt suggests that high concentrations of Cl are not necessary to saturate the melt in NaCl or KCl.Cl-saturation of the melt and coexisting MVP might have been produced by a drop in Cl solubility due to the near-haplogranitic composition of the granitoids after extreme fractionation, probably enhanced by fluctuating reductions of the emplacement pressure in the brittle monzogranite host. Liquid immiscibility, based in the differential viscosity and density among alkali-chloride saturated hydrosaline melt, aluminosilicate felsic melt, and H2O-rich volatiles is likely to have crystallized halite and sylvite from exsolved hydrosaline melt. High degrees of undercooling might have been important at the time of alkali-chloride exsolution. The effectiveness of alkali-chloride separation from the melt at magmatic temperatures is in line with the interpretation of “halite subtraction” as a necessary process to understand the origin of the “halite trend” in highly saline fluid inclusions from porphyry copper and other hydrothermal mineralizations, despite the absence of the latter in the Cerro Baritina aplites, where this process preceded the exsolution of halite-undersaturated fluids.Pervasive alteration of the monzogranite country rock as alkali-metasomatic mineral assemblages, the mineral chemistry of some species, and the association of weak molybdenite mineralization are compatible with the activity of alkaline hypersaline fluids, most likely exsolved during the earliest stages of aplite consolidation.  相似文献   

13.
石盐的流体包裹体成分可提供古流体组成的物理化学信息,用以探查卤水组成变化及环境演化规律等。四川盆地位于上扬子地台,其中的早-中三叠纪沉积建造是中国海相找钾的有利层位之一。获取石盐沉积时期的卤水成分信息,是深刻认识四川盆地古海水蒸发浓缩程度的重要途径。文章利用激光剥蚀电感耦合等离子体质谱法,对采自川东地区长平3井嘉陵江组的石盐流体包裹体开展了化学组成分析,结果显示古卤水化学类型为Mg_SO4型;流体包裹体中的ρ(K~+)与现代海水浓缩到钾石盐析出阶段的ρ(K~+)基本一致,可能揭示了盆地三叠纪时期古卤水已达到钾石盐析出阶段,对四川盆地沉积环境演化及钾盐成矿规律研究等具有重要的理论意义。  相似文献   

14.
Mo-Bi mineralization occurs in subvertical and subhorizontal quartz-muscovite-± K-feldspar veins surrounded by early albitic and later K-feldspathic alteration halos in monzogranite of the Archean Preissac pluton, Abitibi region, Québec, Canada. Molybdenite is intergrown with muscovite in the veins or associated with K-feldspar in the alteration halos. Mineralized veins contain five main types of fluid inclusions: aqueous liquid and liquid-vapor inclusions, aqueous carbonic liquid-liquid-vapor inclusions, carbonic liquid and vapor inclusions, halite-bearing aqueous liquid and liquid-vapor inclusions, trapped mineral-bearing aqueous liquid and liquid-vapor inclusions. The carbonic solid in frozen carbonic and aqueous-carbonic inclusions melts in most cases at −56.7 ± 0.1 °C indicating that the carbonic fluid consists largely of CO2. All aqueous inclusion types and the aqueous phase in carbonic inclusions have low initial melting temperatures (≥70 °C), requiring the presence of salts other than NaCl. Leachate analyses show that the bulk fluid contains variable proportions of Na, K, Ca, Cl, and traces of Mg and Li. The following solids were identified in the fluid inclusions by SEM-EDS analysis: halite, calcite, muscovite, millerite (NiS), barite and antarcticite (CaCl2 · 6H2O). All are interpreted to be trapped phases except halite which is a daughter mineral, and antarcticite which formed during sample preparation (freezing). Aqueous inclusions homogenize to liquid at temperatures between 75 °C and 400 °C; the mode is 375 °C. Aqueous-carbonic inclusions homogenize to liquid or vapor between 210 °C and 400 °C. Halite-bearing aqueous inclusions homogenize by halite dissolution at approximately 170 °C. Aqueous inclusions containing trapped solids exhibit liquid-vapor homogenization at temperatures similar to those of halite-bearing aqueous inclusions. Temperatures of vein formation, based on oxygen isotopic fractionation between quartz and muscovite, range from 342 °C to 584 °C. The corresponding oxygen isotope composition of the aqueous fluid in equilibrium with these minerals ranges from 1.2 to 5.5 per mil with a mean of 3.9 per mil, suggesting that the liquid had a significant meteoric component. Isochores for aqueous fluid inclusions intersect the modal isotopic isotherm of 425 °C at pressures between 590 and 1900 bar. A model is proposed in which molybdenite was deposited owing to decreasing temperature and/or pressure from CO2-bearing, moderate to high salinity fluids of mixed magmatic-meteoric origin that were in equilibrium with K-feldspar and muscovite. These fluids resulted from the degassing of a monzogranitic magma and evolved through interaction with volcanic (komatiitic) and sedimentary country rocks. Received: 6 February 1997 / Accepted: 28 January 1998  相似文献   

15.
Fluid inclusions that bear halite daughter minerals were discovered in volcanic rocks at Pingnan area in the Dongying sag. The samples of the fluid inclusions collected from the BGX-15 well drill cores are hosted in quartz of diorite-porphyrite. The daughter minerals are identified as NaCl crystals after being observed under a microscope and analyzed by in situ Raman spectroscopy at −185°C. The results of micro-thermal analysis show that the homogenization temperatures of primary fluid inclusions are between 359 and 496°C, and the salinities of fluid inclusions are from 43.26 to 54.51 wt-%. All fluid inclusions in the studied samples can be divided into five types including primary fluid inclusions and secondary fluid inclusions. The fact that five types of fluid inclusions were symbiotic in the same quartz grain implies that immiscibility happened in magma. Due to the decrease in temperature and pressure during the ascent of magma, the fluids became intensively immiscible. This process accelerates the degassing of CO2 from magma, but the remnant fluids with high salinity are preserved in fluid inclusions. Thus, the primary fluid inclusions are mainly in NaCl-H2O fluids and poor in CO2. The results of our study indicate that the degassing of magma and accumulation of CO2 gas at the Pingnan area are relative to the immiscibility of high salinity fluids. This discovery is important because it can help us have a further understanding of the mechanism of magma degassing and accumulation of the inorganic CO2 in eastern China. Translated from Acta Geologica Sinica, 2006, 80(11): 1699–1705 [译自: 地质学报]  相似文献   

16.
Ordovician limestones in the Francon quarr on the island of Montreal, Quebec, are host to three sills of Cretaceous age composed of phonolite that has been extensively altered to dawsonite. An interesting feature of the sills is the presence of abundant vugs containing a wide variety of minerals, including several in which one or more high field strength elements (Zr, Hf, Nb, Ti) is a major component. The most important of these latter minerals is weloganite, a rare strontium zirconium hydrous carbonate, first identified in the Francon, quarry. Four types of inclusions have been recognized in vug minerals: aqueous, aqueous-carbonic, carbonic and solidbearing. Aqueous inclusions homogenize at temperatures mainly between 70° and 170°C and between 230° and 390°C. The homogenization temperatures of primary inclusions cluster around 350°C. Aqueous inclusions and the aqueous phase in aqueous-carbonic inclusions have salinities ranging between 10 and 24 eq.wt.% NaCl equivalent. Primary aqueous-carbonic inclusions have low XCO2 (<0.03), whereas secondary aqueous-carbonic inclusions can have high XCO2 (>0.7); carbonic inclusions are all secondary. Nahcolite, dawsonite and weloganite occur as daughter minerals or trapped solids. Nahcolite and possibly natron or mirabilite appear to form in frozen inclusions. Analyses of fluid inclusion decrepitates detected high concentrations of Na, Cl, Al, S, and C. The extraordinarily high concentration of Al in the fluid (possibly exceeding 1 wt.%) suggests a pH of approximately 10. Pressure and temperature conditions, estimated from stratigraphic reconstruction and the isochores of primary aqueous fluid inclusions, were 450 bar and 360 to 400°C, respectively. The relatively high temperatures and compositions of primary fluid inclusions suggest that vug filling was the result of mineral precipitation from an orthomagmatic fluid. A model is proposed in which a partially crystallized phonolite melt started exsolving a homogeneous low XCO2 fluid immediately prior to or after intrusion. Sodium, aluminium, chlorine, fluorine, sulphur and HFSE elements such as Zr, Hf, Nb and Ti were partitioned into the hydrous phase, in the case of Zr, possibly to a concentration of 300 ppm. The near horizontal orientation of the sills and the chilled margins, produced by quenching of the magma, created a tight seal that inhibited escape of the fluids. As a result, the phonolite stewed in its own juices long after crystallization, giving rise to widespread replacement of primary igneous minerals by dawsonite, and precipitation of this and other minerals in vugs. Once the sills had colled to temperatures between 200 and 300°C, the aqueous fluid exsolved a high CO2 fluid which was trapped as the secondary three-phase type II and type III inclusions. Decreasing temperature is considered to have been the principal control of mineralization, although in the case of the lower temperature minerals, decreased bicarbonate or carbonate ion activity, and a lower dielectric constant, as a result of CO2 exsolution, may have played a role in the deposition of HFSE-bearing minerals.  相似文献   

17.
Summary The low-pressure emplacement of a quartz diorite body in the metapelitic rocks of the Gennargentu Igneous Complex (Sardinia, Italy) produced a contact metamorphic aureole and resulted in migmatisation of part of the aureole through partial melting. The leucosome, formed by dehydration melting involving biotite, is characterised by granophyric intergrowth and abundant magnetite crystals. A large portion of the high temperature contact aureole shows petrographic features that are intermediate between quartz diorite and migmatite s.s. (i.e. hybrid rocks). A fluid inclusion study has been performed on quartz crystals from the quartz diorite and related contact aureole rocks, i.e. migmatite sensu stricto (s.s.) and hybrid rocks. Three types of fluid inclusions have been identified: I) monophase V inclusions, II) L + V, either L-rich or V-rich aqueous saline inclusions and III) multiphase V + L + S inclusions. Microthermometric data characterised the trapped fluid as a complex aqueous system varying from H2O–NaCl–CaCl2 in the quartz diorite to H2O–NaCl–CaCl2–FeCl2 in the migmatite and hybrid rocks. Fluid salinities range from high saline fluids (50 wt% NaCl eq.) to almost pure aqueous fluid. Liquid-vapour homogenisation temperatures range from 100 to over 400 °C with an average peak around 300 °C. Temperatures of melting of daughter minerals are between 300 and 500 °C. Highly saline liquid- and vapour-rich inclusions coexist with melt inclusions and have been interpreted as brine exsolved from the crystallising magma. Fluid inclusion data indicate the formation of fluid of high iron activity during the low-pressure partial melting and a fluid mixing process in the hybrid rocks.  相似文献   

18.
Three successive metamorphic stages M1, M2 and M3 have been distinguished in polymetamorphic granulite facies quartz-feldspathic gneisses from the Seiland Igneous Province, Caledonides of northern Norway. An early period of contact metamorphism (M1; 750–950°C, ca. 5 kbar) was followed by cooling, accompanied by strong shearing and recrystallization at intermediate-P granulite facies conditions (M2; 700–750°C, 5–6kbar). High-P granulite facies (M3; ca. 700°C, 7–8 kbar) is related to recrystallization in narrow ductile shear zones and secondary growth on M2 minerals. On the basis of composition, fluid inclusions in cordierite, quartz and garnet can be divided into three major types: (1) CO2 inclusions; (2) mixed CO2–N2 inclusions; (3) N2 inclusions. Fluid chronology and mineral assemblages suggest that the earliest inclusions consist of pure CO2 and were trapped at the M1 contact metamorphic episode. A carbonic fluid was also present during the intermediate-P granulite facies M2 metamorphism. The CO2-rich inclusions in M2 garnet can be divided into two generations, an early lower-density and a late higher-density, with isochores crosscutting the P-T box of M2 and M3, respectively. The nitrogen-rich fluids were introduced at a late stage in the fluid evolution during the high-P M3 event. The mixed CO2–N2 inclusions, with density characteristics compatible with M3 conditions, are probably produced from intersection between pre-existing pure CO2 inclusions and N2 fluids introduced during M3. The fluid inclusion data agree with the P-T evolution established from mineral assemblages and mineral chemistry.  相似文献   

19.
１．Ｉｎｔｒｏｄｕｃｔｉｏｎ　ＴｈｅＱｉｎｌｉｎｇＤａｂｉｅｏｒｏｇｅｎｉｃｂｅｌｔｗａｓｆｏｒｍｅｄｂｙｃｏｌｌｉｓｉｏｎｂｅｔｗｅｅｎｔｈｅＮｏｒｔｈＣｈｉｎａａｎｄＹａｎｇｔｚｅｂｌｏｃｋｓ．Ｔｈｅｃｏｒｅｐａｒｔｏｆｔｈｅｏｒｏｇｅｎｉｃｂｅｌｔｃｏｎｓｉｓｔｓｏｆｓｅｖｅｒａｌｍｅｔａｍｏｒｐｈｉｃｒｏｃｋｇｒｏｕｐｓ,ｉｎｃｌｕｄｉｎｇｔｈｅＤａｂｉｅ（Ｔｏｎｇｂａｉ）ｃｏｍｐｌｅｘ,Ｈｏｎｇ’ａｎ（Ｓｕｓｏｎｇ）ｇｒｏｕｐ,ＳｕｊｉａｈｅｇｒｏｕｐａｎｄＳｕｉｘｉａｎ（Ｙａｏ…  相似文献   

20.
Eclogites occur as isolated blocks in melanges of both the Samana Peninsula, Dominican Republic, and the Franciscan Complex, California, USA. In some of these eclogites, fluid inclusions were found in omphacite and sodic-calcic amphibole grains. Textures show that non-planar populations of fluid inclusions formed during growth of clinopyroxene and amphibole. In addition, planar arrays of secondary fluid inclusions are found along healed cracks. Homogenization temperatures to liquid were used to calculate isochores for the fluid inclusions. These data were compared with petrologic geothermobarometry. Temperature conditions of 500–700° C were estimated from garnetclinopyroxene geothermometry. The jadeite contents of omphacite indicate minimum pressures of 8–11 kbar in this temperature range. The P-T estimates agree well with calculated isochores for primary fluid inclusions from the Samana Peninsula, and show some overlap for both primary and secondary fluid inclusions from the Franciscan Complex. Salinities of 1.2–5.3 wt% NaCl equiv. were estimated for both primary and secondary fluid inclusions from Samana and Franciscan eclogites. These data suggest that low-salinity aqueous fluids attended eclogite-facies metamorphism and perhaps retrograde metamorphism in both subduction complexes. The salinities and densities of fluid inclusions in eclogites from the Samana Peninsula and the Franciscan Complex resemble those of counterparts from garnet amphibolites of the Catalina Schist, southern California. An external source for such fluids is suggested by their homogeneous populations coupled with their low salinities. Geologic evidence suggests that the Samana and Franciscan eclogites may have been derived from a Catalina-like source terrane. The Catalina rocks are inferred to have interacted with large volumes of sediment-derived fluid during subduction zone metamorphism at similar P but higher T conditions than those determined for Samana and Franciscan eclogite blocks. These results contrast with data for fluid inclusions from eclogites of the Monviso area, western Alps. The Monviso eclogites yield similar estimates for metamorphic P-T to those obtained in this study, but contain fluid inclusions of brine and of other saline aqueous fluids, all of which are less dense than expected for incorporation at the reported eclogite-facies conditions. The differences between the properties of fluid inclusions from the ecologites and garnet amphibolites of the Samana-Franciscan-Catalina subduction complexes and those of Monviso probably reflect differences between fluid-flow regimes during metamorphism.  相似文献   

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