Experimental study of fluorine and chlorine contents in mica (biotite) and their partitioning between mica,phonolite melt,and fluid

This paper reports the results of a study of the composition of mica (biotite) crystallizing in the system of phonolite melt-Cl- and F-bearing aqueous fluid at T ～ 850°C, P = 200 MPa, and \(f_{O_2 } \) = Ni-NiO, as well as data on F and Cl partitioning between coexisting phases. It was established that Cl content in mica is significantly lower than in phonolite melt and, especially, in fluid. Fluorine shows a different behavior in this system: its content in mica is always higher than in phonolite melt but lower than in fluid. The mica-melt partition coefficients of Cl and F also behave differently. The Cl partition coefficient gradually increases from 0.17 to 0.33 with increasing Cl content in the system, whereas the partition coefficient of F sharply decreases from 3.0 to 1.0 with increasing total F content. The apparent partition coefficients of F between biotite and groundmass (melt) in various magmatic rocks are usually significantly higher than the experimental values. It was supposed that the higher ^Bt/glassD_F values in natural samples could be related to the influence of later oxidation reactions, reequilibration of biotite at continuously decreasing \(f_{H_2 O} \)/f _HF ratio, and an increase in this coefficients with decreasing total F content in the system.     

A combined EMPA and LA-ICP-MS study of Li-bearing mica and Sn–Ti oxide minerals from the Qiguling topaz rhyolite (Qitianling District,China): The role of fluorine in origin of tin mineralization

The Sn-rich Qiguling topaz rhyolite dike intrudes the Qitianling biotite granite of the Nanling Range in southern China; the granite hosts the large Furong Sn deposit. The rhyolite dike is typically peraluminous, volatile-enriched, and highly evolved. Whole-rock F and Sn concentrations attain 1.9 wt.% and 2700 ppm, respectively. The rhyolite consists of a fine-grained matrix formed by quartz, feldspar, mica and topaz, enclosing phenocrysts of quartz, feldspar and mica; it is locally crosscut by quartz veinlets. Lithium-bearing micas in both phenocrysts and the groundmass can be classified as primary zinnwaldite, “Mus-Ann” (intermediate member between annite and muscovite), and secondary Fe-rich muscovite. Topaz is present in the groundmass only; common fluorite occurs in the groundmass and also in a specific cassiterite, rutile and fluorite (Sn–Ti–F) assemblage. Cassiterite and rutile are the only Sn and Ti minerals; both cassiterite and Nb-rich rutile are commonly included in the phenocrysts. The Sn–Ti–F assemblage is pervasive, and contains spongy cassiterite in some cases; cassiterite also occurs in quartz veinlets which cut the groundmass. Electron microprobe and LA-ICP-MS compositions were used to study the magmatic and hydrothermal processes and the role of F in Sn mineralization. The presence of zinnwaldite and “Mus-Ann”, which are respectively representative of early and late mica crystallization during magma differentiation, also suggests a significant decrease in f(HF)/f(H₂O) of the system. Cassiterite included in the zinnwaldite phenocrysts is suggested to have crystallized from the primary magma at high temperature. Within the Sn–Ti–F aggregates, rutile crystallized as the earliest mineral, followed by fluorite and cassiterite. Spongy cassiterite containing inclusions of the groundmass minerals indicate a low viscosity of the late fluid. The cassiterite in the quartz veinlets crystallized from low-temperature hydrothermal fluids, which possibly mixed with meteoric water. In general, cassiterite precipitated during both magmatic and hydrothermal stages, and over a range of temperatures. The original fluorine and tin enrichments, f(HF)/f(H₂O) change in the residual magma, formation of Ca,Sn,F-rich immiscible fluid, decrease of the f(HF) during groundmass crystallization, and mixing of magma-derived fluids with low-saline meteoric water during the late hydrothermal stage, are all factors independently or together responsible for the Sn mineralization in the Qiguling rhyolite.     

Geochemical characteristics of biotite from felsic intrusive rocks around the Sisson Brook W–Mo–Cu deposit,west-central New Brunswick: An indicator of halogen and oxygen fugacity of magmatic systems

The Sisson Brook W–Mo–Cu deposit was formed by hydrothermal fluids likely related to the Nashwaak Granites (muscovite–biotite granite, Group I; and biotite granite, Group II) and related dykes (biotite granitic dykes, Group III; and a feldspar–biotite–quartz porphyry dyke, Group IV). Chemical data obtained using EPMA and LA-ICP-MS data of primary magmatic biotites were used to investigate magmatic processes and associated hydrothermal fluids.Trace element features of biotite in the Group I two-mica granite suggest other magmatic processes along with a simple fractional crystallization. The K/Rb ratios and compatible elements (Cr, Ti, Co, V, and Ba) in biotite from Groups II, III, and IV decrease, whereas incompatible elements including Ta, Tl, Ga, Cs, Li, and Sn increase with magma fractionation. No correlation of Cu, W and Mo with K/Rb ratios is evident, suggesting that partitioning of Cu, W, and Mo into biotite may not be entirely controlled by magma fractionation.Halogen fugacity of the parental magma of the Nashwaak Granites and related dykes, calculated from zircon saturation temperature shows that Group I has high fHF/fCl ratios (broadly higher than 0), similar to the plutons at the Henderson porphyry Mo deposit. The fHF/fCl ratios of the other groups are generally lower than 0, comparable to the Santa Rita porphyry Cu deposit. The fH₂O/fHCl and fH₂O/fHF ratios inferred from biotite in the Nashwaak Granites and related dykes range from 3 to 5 and from 4 to 5, respectively. The inferred oxygen fugacity shows that the dyke phases (Groups III and IV) have the oxygen fugacity around the nickel–nickel oxide buffer. The plutonic phases (Groups I and II) have the oxygen fugacity around the quartz–fayalite–magnetite (QFM) buffer at high temperatures and oxidized to nickel–nickel oxide buffer at lower temperatures. This oxidation process in the plutonic phases (Groups I and II) could be caused by H₂ release at or near H₂O vapor saturation at high H₂O/Fe^2 +. The magma associated with the biotite dykes (Group III) is more likely the source of the hydrothermal fluids at the Sisson Brook deposit since it has the highest differentiation degree and seems to have formed in an oxidized setting, necessary for Mo to concentrate in the late stage fluids.     

Coupled micro-faulting and pressure solution creep overprinted on quartz schist deformed by intracrystalline plasticity during exhumation of the Sambagawa metamorphic rocks,southwest Japan

In the Sambagawa schist, southwest Japan, while ductile deformation pervasively occurred at D₁ phase during exhumation, low-angle normal faulting was locally intensive at D₂ phase under the conditions of frictional–viscous transition of quartz (c. 300 °C) during further exhumation into the upper crustal level. Accordingly, the formation of D₂ shear bands was overprinted on type I crossed girdle quartz c-axis fabrics and microstructures formed by intracrystalline plasticity at D₁ phase in some quartz schists. The quartz c-axis fabrics became weak and finally random with increasing shear, accompanied by the decreasing degree of undulation of recrystallized quartz grain boundaries, which resulted from the increasing portion of straight grain boundaries coinciding with the interfaces between newly precipitated quartz and mica. We interpreted these facts as caused by increasing activity of pressure solution: the quartz grains were dissolved mostly at platy quartz–mica interface, and precipitated with random orientation and pinned by mica, thus having led to the obliteration of existing quartz c-axis fabrics. In the sheared quartz schist, the strength became reduced by the enhanced pressure solution creep not only due to the reduction of diffusion path length caused by increasing number of shear bands, but also to enhanced dissolution at the interphase boundaries.     

Chemistry of Micas in Rare-Metal Granitoids and Associated Rocks,Eastern Desert,Egypt

Paragenetic, textural, and chemical characteristics of micas from 10 rare-metal granitic stocks and the associated greisens were examined in order to identify the metallogenetic processes of the host granitoids. The investigated granitoids and type occurrences can be categorized as: (1) metaluminous, Nb + Zr + Y-enriched alkali granite (e.g., Hawashia, Ineigi, and a stock northwest of Um Naggat); (2) peraluminous, Ta > Nb + Sn ± W + Be-enriched Li-albite granites (e.g., Nuweibi, Igla, and Abu Dabbab); and (3) metasomatized, Nb » Ta + Sn + Zr + Y + U ± Be ± W-enriched apogranites (e.g., Um Ara, Abu Rusheid, Mueilha, and Homr Akarem).

Mica of the alkali granite is of the annite-siderophyllite series, and is characterized by an average FeO? of 28.14, low MgO of 0.05, a mean Fe?/(Fe? + Mg)_atom. value of 0.996, TiO₂ of 0.69, enhanced Al₂O₃ of 14.91, MnO of 0.58, Li₂O of 0.26, and moderate to low F of 0.86. These characteristics are representative of the relatively highly evolved nature of the annite-siderophyllite-bearing magmas. The micas closely resemble those of the anorogenic pegmatites and A-type granites.

Primary mica of the Li-albite granites is compositionally constrained between zinnwaldite in the lower zones, and white mica in the apical, more evolved zone, and is associated with columbite-tantalite, topaz, and fluorite. The occurrence of zinnwaldite with high contents of Mn and F indicates its stabilization at rather low temperatures in Li- and F-rich sodic melts. The restriction of white mica with lower Mn, F, and Li contents to the apical zones can be attributed to either volatile degassing or to the beginning of topaz crystallization. These two factors brought about an evolutionary trend for micas, which contrasts with the documented trends of Li-micas in other Li-granites (i.e., from Li-siderophyllite or Li-muscovite to lepidolite).

Micas range in composition between white mica in the lower unaltered zones of the apogranites and Li-siderophyllite-zinnwaldite in the apical microclinized and albitized zones; this systematic compositional change appears to reflect roofward increasing in μ_KF and μ_LiF of the exsolved fluids. Columbite, cassiterite, zircon, xenotime, beryl, and fluorite are common associates of the zinnwaldites. However, white micas from the greisenized apogranite and endogreisen veins have diminishing Li contents. The subsolidus formation of zinnwaldite and Li-siderophyllite in the apogranites, and white mica in the associated greisens, represent transitions from magmatic to hydrothermal environments under the influence of decreasing P, T, salinity, and alkalinity of the exsolved fluids.     

Mineralogy and microchemistry of the Egat gold deposit, South Eastern Desert of Egypt

Gold-bearing quartz lodes from the Egat gold mine, South Eastern Desert of Egypt, are associated with pervasively silicified, highly sheared ophiolitic metagabbro and island-arc metavolcanic rocks. The mineralized quartz veins and related alteration haloes are controlled by NNW-trending shear/fault zones. Microscopic and electron probe microanalyses (EPMA) data of the ore and gangue minerals reveal that fine-grained auriferous sulfarsenides represent early high-temperature (355–382 °C) phases, with formation conditions as (fS₂?=??10, and fO₂ around ?31). A late, low-temperature (302–333 °C) assemblage includes coarse pyrite, arsenopyrite, and free-milling gold grains (88–91 wt.% Au), with formation conditions as (fS₂?=??8 and fO₂ around ?30). Gold was impounded within early sulfarsenides, while free-milling gold blebs occur along microfractures in quartz veins and as inclusions in late sulfides. Infiltration of hydrothermal fluids under brittle–ductile shear conditions led to mobilization of refractory Au from early sulfarsenide phases and reprecipitated free gold, simultaneous with silicification of the host rocks. The positive correlation between Au and As favors and verifies the use of As as the best pathfinder for gold targets, along the NNW-trending shear zones.     

Volatile contents of phlogopite micas from South African kimberlite

Phlogopite micas from nodules in South African kimberlites were analyzed for major elements with the electron microprobe and for volatile contents by high temperature mass spectrometry. The micas are from primary- (deformed) and secondary- (undeformed) textured grains in perodotite xenoliths, glimmerites, MARID (mica-amphibole-rutile-ilmenite-diopside) suite nodules and a mica megacryst. The major element and volatile contents of micas exhibiting these modes of occurrence overlap to a greater extent than indicated in previous studies. Concentrations of volatile species occupying structurally defined crystallographic sites (H₂O, F, Cl) are greater for many of the micas than predicted on the basis of the mica formula, particularly for the glimmerite and MARID suite samples. A correlation exists between micas with tetrahedral and octahedral cation deficiencies and those with excess H₂O, F and Cl. Substitution of H⁺ for tetrahedral and possibly octahedral cations may be responsible for the excess H₂O in these micas. Except for one sample, the major element and volatile data for the peridotite, glimmerite and MARID suite micas indicate that they crystallized at oxygen fugacities below the quartz-fayalite-magnetite buffer. F and K₂O are in the correct proportion in the micas to provide the source for these elements in alkali basalts, but not in mid-ocean ridge basalts. Kaersutite amphibole is a more likely source of potassium and fluorine in mid-ocean ridge basalts.     

Mineral chemistry of hydrothermal biotite from the Kahang porphyry copper deposit (NE Isfahan), Central Province of Iran

The Kahang porphyry Cu deposit, located northeast of Isfahan city in central of Iran, is associated with a composite Miocene stock and ranges in composition from diorite through granodiorite to quartz-monzonite. Field observations and petrographic studies show that the emplacement of the Kahang stock occurred in several pulses, each associated with its related hydrothermal activity. Early hydrothermal alteration started with a potassic style in the central part of the system and produced a secondary biotite–K-feldspar–magnetite assemblage accompanied by chalcopyrite and pyrite mineralization. Propylitic alteration that took place at the same time as the potassic alteration occurred in the peripheral portions of the stock. Subsequent phyllic alteration overprinted earlier potassic and propylitic alterations. Biotite grains from the potassic and phyllic zones show distinct chemical compositions. The FeO, TiO₂, MnO, K₂O, and Na₂O concentrations in biotite from the phyllic alteration zone are lower than those from the potassic alteration zone. The F and Cl contents of biotite from the potassic alteration zone display relatively high positive correlation with the X_Mg. The fluorine intercept values [IV(F)] from the potassic and phyllic alteration zones are strongly correlated with the fluorine/chlorine intercept values [IV(F/Cl)]. Biotite geothermometry for the potassic and phyllic alteration zones, based on the biotite geothermometer of Beane (1974), yields a temperature range of 422° to 437 °C (mean = 430 °C) and 329° to 336 °C (mean = 333 °C), respectively. The position of data in log (X_F/X_OH) ratio vs. X_Mg and X_Fe diagram suggests that biotite formed under dissimilar composition and temperature conditions in the potassic and phyllic alteration zones. Calculated log fugacity ratios of (fH₂O/fHF), (fH₂O/fHCl), and (fHF/fHCl) show that hydrothermal fluids associated with the potassic alteration were distinctively different from those fluids associated with the phyllic alteration zone at Kahang porphyry Cu deposit. The results of this research indicate that the chemistry of biotite is related to the chemical composition of the magma and the prevailing physical conditions during crystallization.     

Significant Li isotope fractionation in geochemically evolved rare element-bearing pegmatites from the Little Nahanni Pegmatite Group,NWT, Canada

Lithium isotope signatures of whole rock pegmatite samples and mineral separates from the rare element-bearing Little Nahanni Pegmatite Group, NWT, and whole rock samples from nearby granitic intrusions were measured. Correlation of the Li isotopic values from the pegmatite dikes with whole rock trace element geochemistry, mineralogy and primary textural evidence reflect mechanisms of Li isotopic fractionation during pegmatite formation. The heavier δ⁷Li signatures within the broad range measured from whole rock LNPG samples (? 0.94‰ to + 11.36‰) are related to the consolidation of the final ~ 15% melt fraction of a volatile-rich peraluminous magma in the late stages of magmatic fractionation. Rock-forming minerals (quartz, albite, spodumene and mica) display δ⁷Li signatures that indicate consolidation of the dikes under variable, non-equilibrium conditions. Lithium isotope signatures of relatively cool, highly evolved peraluminous magmas reflect the build-up of fluxes (e.g., H₂O and F) and provide a qualitative assessment of the state of mineral/melt chemical equilibrium.     

The characteristics of volatile components and alkaline metasomatism in main skarn-type iron deposits in China and their role in ore formation

Skarns, ores and hydrothermally metasomatic rocks associated with some major skarn iron deposits in China contain abundant volatile components, such as F, Cl and H₂O. Alkaline (sodic or potassic) metasomatism is obviously evident in the magmatic and other alumo-silicate wall rocks. They may serve as important ore-searching indicators. In this paper, the probable source of iron fluids, transport forms of iron and conditions of precipitation of magnetite are also discussed. From the studies of major skarn iron deposits in China, the authors hold that volatile components, such as F, Cl, H₂O, etc., and alkaline (K, Na) metasomatism play a very important role in the formation of this type of iron deposits^{[1, 2, 3]}.     

Multistage Growth of a Rare-Element, Volatile-Rich Microgranite at Argemela (Portugal)

The small Argemela microgranite body in central Portugal displaysmany of the mineralogical and chemical features characteristicof peraluminous, Li, P-rich, rare-element pegmatites. Its mineralogyconsists predominantly of quartz, albite, white mica (partlyreplaced by lepidolite) and a phosphate of the amblygonite series.K-feldspar is noticeably absent or scarce. Cassiterite, beryland columbite are the main accessories. The microgranite showsextreme enrichment in incompatible elements such as F, P, Rb,Cs, Li, Sn and Be, and extreme depletion in Sr, Ba, Zr and REE.It is highly sodic and strongly peraluminous. The micrograniteoverall is interpreted as a mixture of two components: a crystalmush injected from below (seen in narrow dykes intersected duringdrilling, composed of quartz, albite and phengite) and interpretedas ‘feeders’, overprinted by a second highly evolvedcomponent dominated by Li, F, P (Rb, Cs, Be, Sn, Nb, Ta, etc.)considered as a ‘lubricant’ medium for the ascendingmush and occasionally quenched (quartz, albite, skeletal lepidoliteand amblygonite). This second component has the mineralogicaland chemical characteristics of rare-element pegmatites. Allthese petrological characteristics are magmatic. Only a fewnarrow cross-cutting veinlets with quartz, K-feld-spar and F-pooramblygonite are considered as fluid derived. A model of crystallizationin successive steps is proposed where concentration in fluxingagents (F, Li, P, etc.) is progressively enhanced up to saturationwith the crystallization of magmatic lepidolite and amblygonite. KEY WORDS: petrogenesis; microgranite; pegmatite; volatiles; Portugal ^*Corresponding author.     

A cervelleite-like mineral and other Ag-Cu-Te-S minerals [Ag2CuTeS and (Ag,Cu)2TeS] in gold-bearing veins in metamorphic rocks of the Cycladic Blueschist Unit, Kallianou, Evia Island, Greece

A cervelleite-like mineral, two unnamed silver sulfotellurides in the system Ag-Cu-Te-S [Ag₂CuTeS, (Ag,Cu)₂TeS], Te-rich polybasite and cadmian tetrahedrite occur in gold-bearing quartz veins in metapelites and faults within brecciated marbles of the Cycladic Blueschist Unit in the Kallianou area (southern Evia Island, Greece). The quartz veins and faults are discordant to syn-metamorphic structures and formed during ductile to brittle deformation in the final stages of exhumation of the Styra Nappe extrusion wedge (~21?Ma). Te-rich polybasite (up to 7.4 wt. % Te), cadmian tetrahedrite (up to 12.4 wt. % Cd), together with electrum (23?C54 wt. % Ag) and the sulfotellurides, are the main silver carriers in the mineralization. The two unnamed sulfotellurides, Ag₂CuTeS and (Ag,Cu)₂TeS are believed to be new quaternary minerals in the system Ag-Cu-Te-S. These minerals and the cervelleite-like phase could have exsolved from galena during cooling (below 200°C). Initial temperatures for the formation of the sulfotellurides, in the form of hessite-intermediate solid solution, at Kallianou may be up to 300°C under logfS₂ values between?~ ?11.5 to ?8.3, and logfTe₂ from?~ ?14.8 to ?7.8. The values of logfTe₂ and logfS₂ during re-equilibration (at ~200°C) were constrained to ?19.5 to ?15.2 and to ?15.8 to ?11.5 respectively.     

青海祁漫塔格地区矽卡岩型矿床花岗质岩石矿物学及地质意义

青海祁漫塔格地区位于东昆仑造山带西段,是我国近些年来的重点找矿地区之一。本文对区内与虎头崖矿床I矿带(Fe)、野马泉矿床(Fe)、虎头崖矿床VI矿带(Zn)和卡而却卡矿床B区(Cu)有关的花岗质岩石开展了矿物学研究。结果显示,虎头崖矿床I矿带的斜长石以奥长石为主(An15.0-24.1);虎头崖矿床VI矿带的斜长石主要为钠长石和奥长石(An8.7-20.8);卡而却卡矿床B区的斜长石主要是中长石(An33.8-42.2);野马泉矿床的斜长石主要为奥长石和中长石(An26.2-48.4)。角闪石为典型的钙角闪石,其中,虎头崖矿床I矿带的角闪石属铁浅闪石;卡而却卡矿床B区的角闪石为镁角闪石和铁角闪石。各矿床(带)的黑云母普遍富Fe、Ti、F、Cl,属典型的铁黑云母。矿物学特征显示,各矿床(带)的黑云母结晶于相似的高氧逸度条件下,但在结晶温度和挥发份组成等方面存在差异。黑云母的结晶温度和氧逸度特征与各矿床类型之间未表现出明显的规律性特征。结合前人的研究成果可知,岩浆结晶的温度和氧逸度可能不是控制本区矽卡岩矿床成矿作用类型的主要因素。黑云母的挥发份组成与各成矿元素间表现出明显的规律性特征,其中,以Fe为主的虎头崖矿床I矿带和野马泉矿床的岩浆流体特征基本一致,表现出相对富Cl、贫H2O、F的特点;以Zn为主的虎头崖矿床VI矿带的岩浆流体相对富F贫H2O、Cl;以Cu为主的卡而却卡矿床B区的岩浆流体相对富Cl、H2O贫F,说明岩浆流体不同的挥发份组成可能与不同的矿床类型之间存在密切的联系。综合地质特征和矿物学特征可知,岩浆流体的挥发份组成可能是控制青海祁漫塔格地区矽卡岩矿床成矿作用类型多样性的重要因素之一。     

Li, Be, B concentrations and δ7Li values in plagioclase phenocrysts of dacites from Nea Kameni (Santorini, Greece)

Li, Be, B and δ⁷Li SIMS analyses of plagioclase phenocrysts from the 1040–1941 Niki dacite lava (Nea Kameni, Santorini, Greece) exhibit varied processes. From their anorthite contents alone, the crystals may be segregated into four main types: type-N shows the normal decline in An during crystallisation (An_62–40); type-O has only oscillatory zoning accompanied by resorption surfaces (An_58–39); type-C is complex with high-An cores (subtype C1: An_64–58, subtype C2: An_88–73) and normal rims (An_55–42). Type-A plagioclase with high An content (An_92–82) is found within mafic enclaves. On the basis of their Li concentrations, type-O crystals may be subdivided into subtype O1 with flat Li concentration profiles and subtype O2 with decreasing Li concentration from core to rim. The concentrations of Be and B of all four types show a negative correlation with anorthite content (An), but Li concentration profiles differ amongst the different plagioclase types. Types N and O1, and the cores of type-C, are equilibrated in Li concentration. Types O2 and A, and the mantles of type-C display an initial enrichment in Li, probably from volatile influx into the melt. Consistent with the propensity towards equilibrium with the melt, these crystals display dramatic rim-ward declines in Li concentration. All analysed plagioclase crystals, except for the xenocrystic type-A, have nearly the same Li, Be and B concentrations at their rims. These coincide with the composition of plagioclase microlites in the groundmass, thereby affording estimates of plagioclase-melt partitioning for the light elements: K _Li = 0.19–0.28, K _Be = 0.24–0.38 and K _B = 0.007–0.009. δ⁷Li profiles in type-O2 and type-A phenocrysts manifest an unmistakable inverse relation to Li concentration, with variations of up to ~39 ‰, revealing preferential kinetic diffusion. This may have been driven by Li loss from the melt, most likely through degassing during decompression, perhaps in the course of magma ascent to subsequent eruption. Considering the rapid diffusion of Li in plagioclase, in situ phenocryst analyses may yield useful information about processes leading up to, or even causing, eruptions.     

Comendite Melts of the Early Mesozoic Bimodal Sant Association (Central Mongolia) and Mechanisms of Their Formation

Based on the investigation of melt inclusions using electron and ion microprobe analysis, we estimated the composition, evolution, and formation conditions of magmas producing the the comendites of the Sant bimodal volcanic association (Central Mongolia). The mechanisms of the formation of melts were determined. The primary melt and coexisting crystalline inclusions in quartz from three samples of comendites collected from different parts of the volcanic section were studied. Among the crystalline inclusions, sanidine, zircon, and the REE diortosilicate–chevkinite were identified. The phenocrysts of the comendites were determined to crystallize at temperatures of 880–960°C. The homogeneous glasses of melt inclusions have both trachydacite and rhyolite compositions. They are characterized by high concentrations of Zr, Nb, Rb, Y, Th and REE. Significant differences were determined in concentrations of Li and volatile component (H₂O and F) in the glasses: some of the melts are enriched in these components, whereas other are depleted in them.Analysis of the composition of the glasses of the homogenized melt inclusions in quartz of comendites from the Sant bimodal association allowed us to recognize magmatic processes responsible for formation of the comendite melts. The dominant role among them belongs to crystallization differentiation of the magma, accompanied by a process of liquid immiscibility with participation of fluoride melts.     

江西阳储岭两期岩浆活动与钨成矿作用的关系：来自黑云母地球化学的证据

阳储岭斑岩型W-Mo矿床位于江南造山带中部,是华南地区最早发现的斑岩型钨钼矿床。已探明WO₃资源储量6.13万吨(平均品位0.2%),Mo资源储量1.69万吨(平均品位0.03%～0.06%),其成矿作用与中生代花岗质岩浆活动密切相关。区内发育早期花岗闪长岩和晚期二长花岗斑岩,钨矿体以细脉状和浸染状产于二长花岗斑岩体内,而花岗闪长岩内未见矿化。两期岩浆活动与钨成矿的关系尚不明确,制约其含矿差异性的因素尚不清楚。本文以花岗闪长岩和二长花岗斑岩中的黑云母为研究对象,对比研究两类岩浆结晶分异程度、氧逸度、岩浆流体卤素浓度,探讨其对钨成矿的制约。黑云母主量元素分析结果显示,阳储岭两类岩浆岩均为壳源,但显著不同于S型花岗岩的Mg/(Fe+Mg)和Al^VI值,指示其具有I型花岗岩的特征。黑云母的微量元素信息显示,相对于花岗闪长岩中的黑云母(类型一),二长花岗斑岩中的黑云母(类型二)显示低的K/Rb、Nb/Ta比值,高的Rb、Cs、Nb和Ta含量,表明其分异程度较花岗闪长岩更高,更有利于钨的富集。两类黑云母所指示的岩浆氧逸度均在NNO缓冲线附近,表明其母岩...     

Halogen contents of eclogite facies fluid inclusions and minerals: Caledonides,western Norway

Primary multiphase brine fluid inclusions in omphacite and garnet from low‐ to medium‐temperature eclogites have been analysed for Cl, Br, I, F, Li and SO₄. Halogen contents and ratios provide information about trapped lower crustal fluids, even though the major element (Na, K, Ca) contents of inclusion fluids have been modified by fluid–mineral interactions and (step‐) daughter‐crystal formation after trapping. Halogens in the inclusion fluids were analysed with crush–leach techniques. Cl/Br and Cl/I mass ratios of eclogite fluids are in the range 31–395 and 5000–33 000, respectively. Most fluids have a Cl/Br ratio lower than modern seawater and a Cl/I ratio one order of magnitude lower than modern seawater. Fluids with the lowest Cl/Br and highest Cl/I ratios come from an eclogite that formed by hydration of granulite facies rocks, and may indicate that Br and I are fractionated into hydrous minerals. Reconstructions indicate that the inclusion fluids originally contained 500–4000 ppm Br, 1–14 ppm I and 33–438 ppm Li. Electron microprobe analyses of eclogite facies amphibole, biotite, phengite and apatite indicate that F and Cl fractionate most strongly between phengite (F/Cl mass ratio of 1469 ± 1048) and fluid (F/Cl mass ratio of 0.008), and the least between amphibole and fluid. The chemical evolution of Cl and Br in pore fluids during hydration reactions is in many ways analogous to Cl and Br in seawater during evaporation: the Cl/Br ratio remains constant until the a_H2O value is sufficiently lowered for Cl to be removed from solution by incorporation into hydrous minerals.     

Chemical composition,volatile components,and trace elements in melts of the Karymskii volcanic center,Kamchatka, and Golovnina volcano,Kunashir Island: Evidence from inclusions in minerals

Melt inclusions were examined in phenocrysts in basalt, andesite, dacite, and rhyodacite from the Karymskii volcanic center in Kamchatka and dacite form Golovnina volcano in Kunashir Island, Kuriles. The inclusions were examined by homogenization and by analyzing glasses in more than 80 inclusions on an electron microscope and ion microprobe. The SiO₂ concentrations in the melt inclusions in plagioclase phenocrysts from basalts from the Karymskii volcanic center vary from 47.4 to 57.1 wt %, these values for inclusions in plagioclase phenocrysts from andesites are 55.7–67.1 wt %, in plagioclase phenocrysts from the dacites and rhyodacites are 65.9–73.1 wt %, and those in quartz in the rhyodacites are 72.2–75.7 wt %. The SiO₂ concentrations in melt inclusions in quartz from dacites from Golovnina volcano range from 70.2 to 77.0 wt %. The basaltic melts are characterized by usual concentrations of major components (wt %): TiO₂ = 0.7–1.3, FeO = 6.8–11.4, MgO = 2.3–6.1, CaO = 6.7–10.8, and K₂O = 0.4–1.7; but these rocks are notably enriched in Na₂O (2.9–7.4 wt % at an average of 5.1 wt %, with the highest Na₂O concentration detected in the most basic melts: SiO₂ = 47.4–52.0 wt %. The concentrations of volatiles in the basic melts are 1.6 wt % for H₂O, 0.14 wt % for S, 0.09 wt % for Cl, and 50 ppm for F. The andesite melts are characterized by high concentrations (wt %) of FeO (6.5 on average), CaO (5.2), and Cl (0.26) at usual concentrations of Na₂O (4.5), K₂O (2.1), and S (0.07). High water concentrations were determined in the dacite and rhyodacite melts: from 0.9 to 7.3 wt % (average of 15 analyses equals 4.5 wt %). The Cl concentration in these melts is 0.15 wt %, and those of F and S are 0.06 and 0.01 wt %, respectively. Melt inclusions in quartz from the dacites of Golovnina volcano are also rich in water: they contain from 5.0 to 6.7 wt % (average 5.6 wt %). The comparison of melt compositions from the Karymskii volcanic center and previously studied melts from Bezymyannyi and Shiveluch volcanoes revealed their significant differences. The former are more basic, are enriched in Ti, Fe, Mg, Ca, Na, and P but significantly depleted in K. The melts of the Karymskii volcanic center are most probably less differentiated than the melts of Bezymyannyi and Shiveluch volcanoes. The concentrations of water and 20 trace elements were measured in the glasses of 22 melt inclusions in plagioclase and quartz from our samples. Unusually high values were obtained for Li concentrations (along with high Na concentrations) in the basaltic melts from the Karymskii volcanic center: from 118 to 1750 ppm, whereas the dacite and rhyolite melts contain 25 ppm Li on average. The rhyolite melts of Golovnina volcano are much poorer in Li: 1.4 ppm on average. The melts of the Karymskii volcanic center are characterized by relative minima at Nb and Ti and maxima at B and K, as is typical of arc magmas.     

Part II. Evaluation of Ar-Ar quartz ages: Implications for fluid inclusion retentivity and determination of initial Ar/Ar values in Proterozoic samples

The argon isotope systematics of vein-quartz samples with two different K-reservoirs have been evaluated in detail. Potassium is hosted by ultra-high-salinity fluid inclusions in quartz samples from the Eloise and Osborne iron-oxide-copper-gold (IOCG) deposits of the Mt Isa Inlier, Australia. In contrast, K is hosted by accidentally trapped mica within lower-salinity fluid inclusions of a sample selected from the Railway Fault, 13 km south of the Mt Isa copper mine, Australia. Imprecise apparent ages have been obtained for all of the samples studied and conclusively demonstrate that quartz fluid inclusions are retentive to Ar and have not leaked over billions of years. IOCG samples that host K in fluid inclusions only, have K/Cl values of <1 and the ages obtained represent the maximum ages for mineralization. In contrast, the Railway Fault samples that include accidentally trapped mica have K/Cl values of ?1. Excess ⁴⁰Ar_E plus Cl hosted by fluid inclusions, and radiogenic ⁴⁰Ar_R plus K, are strongly correlated in these samples and define a plane in 3D ⁴⁰Ar-³⁶Ar-K-Cl space. In this case, the plane yields an ‘excess ⁴⁰Ar_E’ corrected age of ∼1030 Ma that is 100’s of Ma younger than nearby Cu-mineralization at Mt Isa. The age is interpreted to reflect ⁴⁰Ar-loss from the accidentally trapped mica into the surrounding fluid inclusions, and is not related to the samples’ age of formation. The initial ⁴⁰Ar/³⁶Ar value of fluid inclusions is widely used to provide information on fluid origin. For the IOCG samples that host K in fluid inclusions only, the initial ⁴⁰Ar/³⁶Ar values are close to the measured values at every temperature of stepped heating experiments. For samples that include accidentally trapped mica, the correction for post-entrapment radiogenic ⁴⁰Ar_R production is significant. Furthermore, because ³⁹Ar_K present in accidentally trapped mica crystals is released at different temperatures to radiogenic ⁴⁰Ar_R lost to the surrounding fluid inclusions, intra-sample ⁴⁰Ar/³⁶Ar variation cannot be reliably documented. The results demonstrate that noble gas analysis is readily applicable to Proterozoic, or older, samples but that if K-mineral impurities are present within quartz the abundance of K must be determined before calculation of mean ⁴⁰Ar/³⁶Ar values that are representative of the samples’ initial composition.     

3-D Mohr circle construction using vein orientation data from Gadag (southern India) – Implications to recognize fluid pressure fluctuation

In this paper orientations of quartz veins from the Archaean age lode-gold bearing region of Gadag (southern India) are used to determine the relative stress and fluid pressure (P_f) conditions by constructing 3-D Mohr circle. Anisotropy of magnetic susceptibility (AMS) analysis of the host massive metabasalt reveals that the magnetic foliation is NW–SE striking, which is related to early NE–SW compression (D1/D2 deformation) that affected the region. The quartz veins have a wide range of orientations, with NW–SE striking veins (steep northeasterly dips) being the most prominent. Vein emplacement is inferred to have taken place under NW–SE compression that is known to have caused late deformation (D3) in the region. It is argued that the NW–SE fabric defined the pre-existing anisotropy and channelized fluid flow during D3. The permeability was initially low, which resulted in high P_f (>σ₂). 3-D Mohr circle analysis indicates that the driving pressure ratio (R′) was 0.94, a condition that favoured fracturing and reactivation of fabric elements (foliations and fractures) having a wide range of orientations. This led to an increase in permeability and fluid flowed (burped) into the fractures. Resulting vein emplacement and sealing of fractures led to a reduction of P_f (<σ₂). It is argued that at this low P_f, NW–SE oriented structures continued to remain susceptible to reactivation and vein emplacement, while fractures of all other orientations were inactive and remained sealed. As a consequence, the study area has a cluster of NW–SE oriented veins. R′ is calculated to be 0.07 from 3-D Mohr circle analysis at low P_f, when fractures with NW–SE orientation only were susceptible to dilation. However, it is envisaged that any emplacement of veins in these fractures would have sealed them, thus reducing the permeability and initiating the next cycle of rise in P_f (>σ₂). Thus, it is concluded that the quartz veins in the Gadag region are a consequence of an interplay between conditions that fluctuated from P_f > σ₂ to P_f < σ₂.