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1.
The aim of this experimental study was to determine the solubility of cassiterite in natural topaz- and cassiterite-bearing granite melts at temperatures close to the solidus. Profiles of Sn concentrations at glass–crystal (SnO 2) interface were determined following the method of (Harrison, T.M., Watson, E.B., 1983. Kinetics of zircon dissolution and zirconium diffusion in granitic melts of variable water content. Contributions to Mineralogy and Petrology 84, 66–72). The cassiterite concentration calculated at the SnO 2–glass interface is the SnO 2 solubility. Experiments were performed at 700–850 °C and 2 kbar using a natural F-bearing peraluminous granitic melt with 2.8 wt.% normative corundum. Slightly H 2O-undersaturated to H 2O-saturated melt compositions were chosen in order to minimize the loss of Sn to the noble element capsule walls. At the nickel–nickel oxide assemblage (Ni–NiO) oxygen fugacity buffer, the solubility of cassiterite in melts containing 1.12 wt.% F increases from 0.32 to 1.20 wt.% SnO 2 with an increasing temperature from 700 to 850 °C. At the Ni–NiO buffer and a given corundum content, SnO 2 solubility increases by 10% to 20% relative to an increase of F from 0 to 1.12 wt.%. SnO 2 solubility increases by 20% relative to increasing Cl content from 0 to 0.37 wt.% in synthetic granitic melts at 850 °C. We show that Cl is at least as important as F in controlling SnO 2 solubility in evolved peraluminous melts at oxygen fugacities close to the Ni–NiO buffer. In addition to the strong effects of temperature and fO 2 on SnO 2 solubility, an additional controlling parameter is the amount of excess Al (corundum content). At Ni–NiO and 850 °C, SnO 2 solubility increases from 0.47 to 1.10 wt.% SnO 2 as the normative corundum content increases from 0.1 to 2.8 wt.%. At oxidizing conditions (Ni–NiO +2 to +3), Sn is mainly incorporated as Sn 4+ and the effect of excess Al seems to be significantly weaker than at reducing conditions. 相似文献
2.
The Variscan Hauzenberg pluton consists of granite and granodiorite that intruded late- to postkinematically into HT-metamorphic rocks of the Moldanubian unit at the southwestern margin of the Bohemian Massif (Passauer Wald). U–Pb dating of zircon single-grains and monazite fractions, separated from medium- to coarse-grained biotite-muscovite granite (Hauzenberg granite II), yielded concordant ages of 320 ± 3 and 329 ± 7 Ma, interpreted as emplacement age. Zircons extracted from the younger Hauzenberg granodiorite yielded a 207Pb– 206Pb mean age of 318.6 ± 4.1 Ma. The Hauzenberg granite I has not been dated. The pressure during solidification of the Hauzenberg granite II was estimated at 4.6 ± 0.6 kbar using phengite barometry on magmatic muscovite, corresponding to an emplacement depth of 16-18 km. The new data are compatible with pre-existing cooling ages of biotite and muscovite which indicate the Hauzenberg pluton to have cooled below T = 250–400 °C in Upper Carboniferous times. A compilation of age data from magmatic and metamorphic rocks of the western margin of the Bohemian Massif suggests a west- to northwestward shift of magmatism and HT/LP metamorphism with time. Both processes started at > 325 Ma within the South Bohemian Pluton and magmatism ceased at ca. 310 Ma in the Bavarian Oberpfalz. The slight different timing of HT metamorphism in northern Austria and the Bavarian Forest is interpreted as being the result of partial delamination of mantle lithosphere or removal of the thermal boundary layer. 相似文献
3.
High-pressure (HP) and ultra-high pressure (UHP) terranes are excellent natural laboratories to study subduction-zone processes. In this paper we give a brief theoretical background and we review experimental data and observations in natural rocks that constrain the nature and composition of the fluid phase present in HP and UHP rocks. We argue that a fluid buffered by a solid residue is compositionally well defined and is either an aqueous fluid (total amount of dissolved solids < 30 wt.%) or a hydrous melt (H 2O < 35 wt.%). There is only a small temperature range of approximately 50–100 °C, where transitional solute-rich fluids exist. A review of available experimental data suggest that in felsic rocks the second critical endpoint is situated at 25–35 kbar and 700 °C and hence must be considered in the study of UHP rocks. Despite this, the nature of the fluid phase can be constrained by relating the peak metamorphic conditions of rocks to the position of the wet solidus even if the peak pressure exceeds the pressure where the wet solidus terminates at the second critical endpoint. Transitional solute-rich fluids are expected in UHP terrains ( P > 30 kbar) with peak temperatures of about 700 ± 50 °C. At higher temperatures, hydrous granitic melts occur whereas at lower temperatures aqueous fluids coexists with eclogite-facies minerals. This argument is complemented by evidence on the nature of the fluid phase from high-pressure terrains. We show that in the diamond-bearing, high-temperature UHP rocks from the Kokchetav Massif there are not only hydrous felsic melts, but probably also carbonate and sulfide melts present. Hydrous quartzo-feldspathic melts are mainly produced in high temperature UHP rocks and their composition is relatively well constrained from experiments and natural rocks. In contrast, constraining the composition of aqueous fluids is more problematic. The combined evidence from experiments and natural rocks indicates that aqueous fluids liberated at the blueschist to eclogite facies transition are dilute. They contain only moderate amounts of LILE, Sr and Pb and do not transport significant amounts of key trace elements such as LREE, U and Th. This indicates that there is a decoupling of water and trace element release in subducted oceanic crust and that aqueous fluids are unable to enrich the mantle wedge significantly. Instead we propose that fluid-present melting in the sediments on top of the slab is required to transfer significant amounts of trace elements from the slab to the mantle wedge. For such a process to be efficient, top slab temperature must be at least 700–750 °C at sub-arc depth. Slab melting is likely to be triggered by fluids that derive from dehydration of mafic and ultramafic rocks in colder (deeper) portions of the slab. 相似文献
4.
Voluminous late Mesoproterozoic monzonite through granite of the Vernon Supersuite underlies an area of approximately 1300 km 2 in the Highlands of northern New Jersey. The Vernon Supersuite consists of hastingsite±biotite-bearing granitoids of the Byram Intrusive Suite (BIS) and hedenbergite-bearing granitoids of the Lake Hopatcong Intrusive Suite (LHIS). These rocks have similar major and trace element abundances over a range of SiO 2 from 58 to 75 wt.%, are metaluminous to weakly peraluminous, and have a distinctive A-type chemistry characterized by high contents of Y, Nb, Zr, LREE, and Ga/Al ratios, and low MgO, CaO, Sr and HREE. Whole-rock Rb–Sr isochrons of BIS granite yield an age of 1116±41 Ma and initial 87Sr/ 86Sr ratio of 0.70389, and of LHIS granite an age of 1095±9 Ma and initial 87Sr/ 86Sr ratio of 0.70520. Both suites have similar initial 143Nd/ 144Nd ratios of 0.511267 to 0.511345 (BIS) and 0.511359 to 0.511395 (LHIS). Values of Nd are moderately high and range from +1.21 to +2.74 in the BIS and +2.24 to +2.95 in the LHIS. Petrographic evidence, field relationships, geochemistry, and isotopic data support an interpretation of comagmatism and the derivation of both suites from a mantle-derived or a juvenile lower crustal parent with little crustal assimilation. Both suites crystallized under overlapping conditions controlled by P– T– fH2O. Lake Hopatcong magma crystallized at a liquidus temperature that approached 900°C and a pressure of about 6 kbar, and remained relatively anhydrous throughout its evolution. Initial P– T conditions of the Byram magma were ≥850°C and about 5.5 kbar. BIS magma was emplaced contemporaneous with, or slightly preceding LHIS magma, and both magmas were emplaced during a compressional tectonic event prior to granulite facies metamorphism that occurred in the Highlands between 1080 and 1030 Ma. 相似文献
5.
Idiomorphic quartz crystals in topaz-bearing granite from the Salmi batholith contain primary inclusions of silicate melt and abundant mostly secondary aqueous fluid inclusions. Microthermometric measurements on melt inclusions give estimates for the granite solidus and liquidus of 640–680°C and 770–830°C, respectively. Using published solubility models for H 2O in granitic melts and the obtained solidus/liquidus temperatures from melt inclusions, the initial water concentration of the magma is deduced to have been approximately 3 wt.% and the minimum pressure about 2 kbar. At this initial stage, volatile-undersaturation conditions of magma were assumed. These results indicate that the idiomorphic quartz crystals are magmatic in origin and thus real phenocrysts. During subsolidus cooling and fracturing of the granite, several generations of aqueous fluid inclusions were trapped into the quartz phenocrysts. The H 2O inclusions have salinities and densities of 1–41 wt.% NaCl eq. and 0.53–1.18 g/cm 3, respectively. 相似文献
6.
The gas and redox chemistry of 100–300 °C geothermal fluids in Iceland has been studied as a function of fluid temperature and fluid composition. The partial pressures of CO 2 in dilute ( mCl<500 ppm) and saline ( mCl>500 ppm) geothermal fluids above 200 °C are controlled by the mineral buffer clinozoisite+prehnite+calcite+quartz. Two buffers are considered to control the H 2S and H 2 partial pressures above 200 °C depending on fluid salinity, epidote+prehnite+pyrite+pyrrhotite for dilute fluids and pyrite+prehnite+quartz+magnetite+anhydrite+clinozoisite+quartz for saline fluids. Below 200 °C, the partial pressures of CO 2, H 2S and H 2 also seem to be buffered but other minerals must be involved. Zeolites are expected to replace prehnite and epidote. Redox potential calculated on the assumption of equilibrium for the H +/H 2 redox couple decreases in dilute geothermal fluids with increasing temperature from about −0.5 V at 100 °C to −0.8 V at 300 °C, whereas saline geothermal fluids at 250 °C display a redox potential of about −0.45 V. A systematic discrepancy between redox couples of about 0.05–0.09 V is observed in the redox potential for the dilute geothermal fluids, whereas redox potentials agree within 0.02–0.04 V for saline geothermal waters. The discrepancies in the calculated redox potential for dilute geothermal fluids are thought to be due to a general lack of equilibrium between CH 4, CO 2 and H 2 and between H 2S, SO 4 and H 2. It is, accordingly, concluded that an overall equilibrium among redox species has not been reached for dilute geothermal fluids whereas it appears to be more closely approached for the saline geothermal fluids. The latter conclusion is based on limited database and should be treated with care. Since the various redox components are not in an overall equilibrium in geothermal fluids in Iceland these fluids cannot be characterised by a unique hydrogen fugacity, oxygen fugacity or redox potential at a given temperature and pressure. 相似文献
7.
Experiments in the system K 2O---MgO---Al 2O 3---SiO 2---H 2O (KMASH) were undertaken with the piston-cylinder-apparatus to study the reactions: 1. (1) phengite±quartz+K,Mg-rich siliceous fluid=feldspar+phologopite+H2O 2. (2) phengite+talc+K,Mg-rich siliceous fluid=phlogopite+quartz/coesite+H2O
at temperatures between 400 and 700°C. The ultrapotassic fluid appearing at pressures above 15 kbar on the low-temperature sides of the corresponding reaction curves, which show positive dP/dT slopes, is probably supercritical. The P-T positions of the reactions are compatible with KMASH mineral reactions studied previously and with melting investigations in the KMASH system undertaken at temperatures higher than 700°C. It is possible that natural rocks, chiefly K-rich metasediments subducted as minor portions of the oceanic crust, could give rise to low-temperature ultrapotassic fluids, mainly at temperatures between 300° to 600°C and pressures between 15 and 30 kbar. The ascending K-rich fluids would penetrate the overlying mantle to metasomatize it. After termination of the subduction process, heating of this mantle material, previously cooled by the subducted lithosphere, could lead to the formation of high-temperature K-rich magmas. 相似文献
8.
The migmatites from Punta Sirenella (NE Sardinia) are layered rocks containing 3–5 vol.% of centimeter-sized stromatic leucosomes which are mainly trondhjemitic and only rarely granitic in composition. They underwent three deformation phases, from D 1 to D 3. The D 1 deformation shows a top to the NW shear component followed by a top to the NE/SE component along the XZ plane of the S 2 schistosity. Migmatization started early, during the compressional and crustal thickening stage of Variscan orogeny and was still in progress during the following extensional stage of unroofing and exhumation. The trondhjemitic leucosomes, mainly consisting of quartz, plagioclase, biotite ± garnet ± kyanite ± fibrolite, retrograde muscovite and rare K-feldspar, are locally bordered by millimeter-sized biotite-rich melanosomes. The rare granitic leucosomes differ from trondhjemitic ones only in the increase in modal content of K-feldspar, up to 25%. Partial melting started in the kyanite field at about 700–720 °C and 0.8–0.9 GPa, and was followed by re-equilibration at 650–670 °C and 0.4–0.6 GPa, producing fibrolite–biotite intergrowth and coarse-grained muscovite. The leucosomes have higher SiO2, CaO, Na2O, Sr and lower Al2O3, Fe2O3, MgO, TiO2, K2O, P2O5, Rb, Ba, Cr, V, Zr, Nb, Zn and REE content with respect to proximal hosts and pelitic metagreywackes. Sporadic anomalous high content of calcium and ferromagnesian elements in some leucosomes is due to entrainment of significant amounts of restitic plagioclase, biotite and accessory phases. The rare granitic leucosomes reveal peritectic K-feldspar produced by muscovite-dehydration melting. Most leucosomes show low REE content, moderately fractionated REE patterns and marked positive Eu anomaly. Proximal hosts and pelitic metagraywackes are characterized by higher REE content, more fractionated REE patterns and slightly negative Eu anomaly. The trondhjemitic leucosomes were generated by H2O-fluxed melting at 700 °C of a greywacke to pelitic–greywacke metasedimentary source-rock. The disequilibrium melting process is the most reliable melting model for Punta Sirenella leucosomes. 相似文献
9.
Strontium chemical diffusion has been measured in albite and sanidine under dry, 1 atm, and QFM buffered conditions. Strontium oxide-aluminosilicate powdered sources were used to introduce the diffusant and Rutherford Backscattering Spectroscopy (RBS) used to measure diffusion profiles. For the 1 atm experiments, the following Arrhenius relations were obtained: Sanidine (Or61), temperature range 725–1075°C, diffusion normal to (001): D=8.4 exp(−450±13 kJ mol−1/RT) m2s−1. Albite (Or1), temperature range 675–1025°C, diffusion normal to (001): D=2.9 × exp(−224±11 kJ mol−1/RT) m2s−1. The alkali feldspars in this and earlier work display a broad range of activation energies for Sr diffusion, which may be a consequence of the thermodynamic non-ideality of the alkali feldspar system and/or the mixed alkali effect. 相似文献
10.
We report compositions of homogenized quartz-hosted melt inclusions from a layered sequence of Li-, F-rich granites in the Khangilay complex that document the range of melt evolution from barren biotite granites to Ta-rich, lepidolite–amazonite–albite granites. The melt inclusions are crystalline at room temperature and were homogenized in a rapid-quench hydrothermal apparatus at 200 MPa before analysis. Homogenization runs determined solidus temperatures near 550 °C and full homogenization between 650 and 750 °C. The compositions of inclusions, determined by electron microprobe and Raman spectroscopy (for H 2O), show regular overall trends of increasing differentiation from the least-evolved Khangilay units to apical units in the Orlovka intrusion. Total volatile contents in the most-evolved melts reach over 11 wt.% (H 2O: 8.6 wt.%, F: 1.6 wt.%, B 2O 3: 1.5 wt.%). Concentrations of Rb range from about 1000 to 3600 ppm but other trace elements could not be measured reliably by electron microprobe. The resulting trends of melt evolution are similar to those described by the whole-rock samples, despite petrographic evidence for albite- and mica-rich segregations previously taken as evidence for post-magmatic metasomatism. Melt variation trends in most samples are consistent with fractional crystallization as the main process of magma evolution and residual melt compositions plot at the granite minimum in the normative Qz–Ab–Or system. However, melts trapped in the highly evolved pegmatitic samples from Orlovka deviate from the minimum melt composition and show compositional variations in Al, Na and K that requires a different explanation. We suggest that unmixing of the late-stage residual melt into an aluminosilicate melt and a salt-rich dense aqueous fluid (hydrosaline melt) occurred. Experimental data show the effectiveness of this process to separate K (aluminosilicate melt) from Na (hydrosaline melt) and high mobility of the latter due to its low viscosity and relatively low density may explain local zones of albitization in the upper parts of the granite. 相似文献
11.
Electron-microprobe analyses are presented for pyroxene, amphibole,and biotite from monzonite, granodiorite, and granite at Finnmarka,Norway. Compositional trends measured in biotite, present inall three rock types, and in amphibole, present in the monzoniteand granodiorite, are markedly atypical and are interpretedas reflecting crystallization under progressively more oxidizingconditions. The average Fe/Fe + Mg for biotites from successivelymore silicic rock types changes from 0.64 0.35 0.28, and foramphiboles changes from 0.58 in the monzonite to 0.29 in thegranodiorite. Analyses of selected areas within amphibole grains in the granodioriteshow marked chemical variations, although single-crystal X-rayphotographs are sharp and do not reveal multiple phases. Onthe basis of 33 such analyses, four coupled substitutions areidentified as operative; the most unusual finding is the relationof 1 Ti cation to 4 Al IV cations in the unit cell. Variationswithin individual amphibole grains of the granodiorite resemblechanges noted in evolution of amphibole composition from monzoniteto granodiorite and are interpreted as reflecting progressiveoxidation. Consideration of these data for the mafic silicates, data forthe opaque oxides, and the extensive formation of sphene inthe granodiorite, has allowed development of schematic reactionsand an overall picture of magmatic environment and evolutionat Finnmarka. Crystallization apparently took place at PH 2oof 1000 bars or less and a temperature of about 700 °C.The trend of oxidation during differentiation is more extremethan any heretofore reported. Amphiboles, as well as biotites,may participate in oxidation reactions and may reflect the oxidation-reductionprocesses that occurred during magmatic evolution. 相似文献
12.
We have experimentally studied the formation of diamonds in alkaline carbonate–carbon and carbonate–fluid–carbon systems at 5.7–7.0 GPa and 1150–1700 °C, using a split-sphere multi-anvil apparatus (BARS). The starting carbonate and fluid-generating materials were placed into Pt and Au ampoules. The main specific feature of the studied systems is a long period of induction, which precedes the nucleation and growth of diamonds. The period of induction considerably increases with decreasing P and T, but decreases when adding a C–O–H fluid to the system. In the range of P and T corresponding to the formation of diamonds in nature, this period lasts for tens of hours. The reactivity of the studied systems with respect to the diamond nucleation and growth decreases in this sequence: Na 2CO 3–H 2C 2O 4·2H 2O–C>K 2CO 3–H 2C 2O 4·2H 2O–C>>Na 2CO 3–C>K 2CO 3–C. The diamond morphology is independent of P and T, and is mainly governed by the composition of the crystallization medium. The stable growth form is a cubo-octahedron in the Na 2CO 3 melt, and an octahedron in the K 2CO 3 melt. Regardless of the composition of the carbonate melt, only octahedral diamond crystals formed in the presence of the C–O–H fluid. The growth rates of diamond varied in the range from 1.7 μm/h at 1420 °C to 0.1–0.01 μm/h at 1150 °C, and were used to estimate, for the first time, the possible duration of the crystallization of natural diamonds. From the analysis of the experimental results and the petrological evidence for the formation of diamonds in nature, we suggest that fluid-bearing alkaline carbonate melts are, most likely, the medium for the nucleation and growth of diamonds in the Earth's upper mantle. 相似文献
13.
The boundary between the Archean cratons and the Eastern Ghats Belt in peninsular India represents a rifted Mesoproterozoic continental margin which was overprinted by a Pan-African collisional event associated with the westward thrusting of the Eastern Ghats granulites over the cratonic foreland. The contact zone contains a number of deformed and metamorphosed nepheline syenite complexes of rift-related geochemical affinities. In addition to the nepheline-bearing rocks, metamorphosed quartz-bearing monzosyenitic bodies can also be identified along the suture in the region between the Godavari-Pranhita graben and the Prakasam Igneous Province. One such occurrence at Jojuru near Kondapalle is geochemically comparable to the nepheline syenites and furnishes a weighted mean concordant U–Th–Pb SHRIMP zircon age of 1263 ± 23 Ma (2 σ), which provides a lower age bracket for the rift-related magmatic activity. The original igneous mineral assemblage in the monzosyenite was partially replaced by the formation of coronitic garnet during the Pan-African metamorphism of the rocks. P– T estimates of garnet corona formation at the interface between clinopyroxene–orthopyroxene–ilmenite clusters and plagioclase indicate mid to upper amphibolite facies condition (5.5–7.0 kbar and 600–700 °C) during the thrust induced deformation and metamorphism associated with the Pan-African collisional tectonics. 相似文献
14.
The pressure dependence of melt viscosities on the join diopside-albite has been studied using falling-sphere viscometry. The five melt compositions investigated are: diopside, Ab 25Di 75, Ab 50Di 50, Ab 75Di 25 and albite. Experiments were performed at 1500° and 1600°C and at pressures of 5, 10, 15, 20 and 25 kbar. The positive and negative pressure dependence of the viscosity of diopside and albite, respectively, were confirmed. All intermediate compositions show an initial decrease in viscosity with increasing pressure; however, melt of Ab 25Di 75 composition passes through a minimum viscosity at approximately 12 kbar and 1600°C. This behavior is analogous to the variation in the viscosity of water with pressure at low temperature. It is suggested that the three-dimensional, fully polymerized, albite structure dominates flow at low pressures. With increasing pressure, disruption of this structure and decrease in the average size of the flow units leads to domination by the diopside structure. The variation in viscosity with composition along the join at one atmosphere can be adequately modelled using the
and
(1965) configurational entropy model with an additional two-lattice configurational entropy of mixing term. The pressure dependence of viscosity in the diopside-albite system, however, cannot be predicted by the model, because there is an absence of information on the pressure dependence of the model parameters. It is probable that relatively polymerized magmas (e.g. rhyolites to SiO2-saturated basalts) show a negative pressure dependence of viscosity to depths where they originate in the lower crust or upper mantle. In contrast, the most depolymerized, naturally-occurring melts, such as strongly SiO2-undersaturated basalts and picrites, may exhibit a viscosity minimum. The viscosity of these melts may be sufficiently high at depths within the upper mantle to inhibit their segregation, rise and eventual eruption at the surface. 相似文献
15.
The solubility of Ti- and P-rich accessory minerals has been examined as a function of pressure and K 2O/Na 2O ratio in two series of highly evolved silicate systems. These systems correspond to (a) alkaline, varying from alkaline to peralkaline with increasing K 2O/Na 2O ratio; and (b) strongly metaluminous (essentially trondhjemitic at the lowest K 2O/Na 2O ratio) and remaining metaluminous with increasing K 2O/Na 2O ratio (to 3). The experiments were conducted at a fixed temperature of 1000 °C, with water contents varying from 5 wt.% at low pressure (0.5 GPa), increasing through 5–10 wt.% at 1.5–2.5 GPa to 10 wt.% at 3.5 GPa. Pressure was extended outside the normal crustal range, so that the results may also be applied to derivation of hydrous silicic melts from subducted oceanic crust. For the alkaline composition series, the TiO2 content of the melt at Ti-rich mineral saturation decreases with increasing pressure but is unchanged with increasing K content (at fixed pressure). The P2O5 content of the alkaline melts at apatite saturation increases with increased pressure at 3.5 GPa only, but decreases with increasing K content (and peralkalinity). For the metaluminous composition series (termed as “trondhjemite-based series” (T series)), the TiO2 content of the melt at Ti-rich mineral saturation decreases with increasing pressure and with increasing K content (at fixed pressure). The P2O5 content of the T series melts at apatite saturation is unchanged with increasing pressure, but decreases with increasing K content. The contrasting results for P and Ti saturation levels, as a function of pressure in both compositions, point to contrasting behaviour of Ti and P in the structure of evolved silicate melts. Ti content at Ti-rich mineral saturation is lower in the alkaline compared with the T series at 0.5 GPa, but is similar at higher pressures, whereas P content at apatite saturation is lower in the T series at all pressures studied. The results have application to A-type granite suites that are alkaline to peralkaline, and to I-type metaluminous suites that frequently exhibit differing K2O/Na2O ratios from one suite to another. 相似文献
16.
Coexisting melt (MI), fluid-melt (FMI) and fluid (FI) inclusions in quartz from the Oktaybrskaya pegmatite, central Transbaikalia, have been studied and the thermodynamic modeling of PVTX-properties of aqueous orthoboric-acid fluids has been carried out to define the conditions of pocket formation. At room temperature, FMI in early pocket quartz and in quartz from the coarse-grained quartz–oligoclase host pegmatite contain crystalline aggregates and an orthoboric-acid fluid. The portion of FMI in inclusion assemblages decreases and the volume of fluid in inclusions increases from the early to the late growth zones in the pocket quartz. No FMI have been found in the late growth zones. Significant variations of solid/fluid ratios in the neighboring FMI result from heterogeneous entrapment of coexisting melts and fluids by a host mineral. Raman spectroscopy, SEM EDS and EMPA indicate that the crystalline aggregates in FMI are dominated by mica minerals of the boron-rich muscovite–nanpingite CsAl 2[AlSi 3O 10](OH,F) 2 series as well as lepidolite. Topaz, quartz, potassium feldspar and several unidentified minerals occur in much lower amounts. Fluid isolations in FMI and FI have similar total salinity (4–8 wt.% NaCl eq.) and H 3BO 3 contents (12–16 wt.%). The melt inclusions in host-pegmatite quartz homogenize at 570–600 °C. The silicate crystalline aggregates in large inclusions in pocket quartz completely melt at 615 °C. However, even after those inclusions were significantly overheated at 650±10 °C and 2.5 kbar during 24 h they remained non-homogeneous and displayed two types: (i) glass+unmelted crystals and (ii) fluid+glass. The FMI glasses contain 1.94–2.73 wt.% F, 2.51 wt.% B 2O 3, 3.64–5.20 wt.% Cs 2O, 0.54 wt.% Li 2O, 0.57 wt.% Ta 2O 5, 0.10 wt.% Nb 2O 5, 0.12 wt.% BeO. The H 2O content of the glass could exceed 12 wt.%. Such compositions suggest that the residual melts of the latest magmatic stage were strongly enriched in H 2O, B, F, Cs and contained elevated concentrations of Li, Be, Ta, and Nb. FMI microthermometry showed that those melts could have crystallized at 615–550 °C. Crystallization of quartz–feldspar pegmatite matrix leads to the formation of H2O-, B- and F-enriched residual melts and associated fluids (prototypes of pockets). Fluids of different compositions and residual melts of different liquidus–solidus P–T-conditions would form pockets with various internal fluid pressures. During crystallization, those melts release more aqueous fluids resulting in a further increase of the fluid pressure in pockets. A significant overpressure and a possible pressure gradient between the neighboring pockets would induce fracturing of pockets and “fluid explosions”. The fracturing commonly results in the crushing of pocket walls, formation of new fractures connecting adjacent pockets, heterogenization and mixing of pocket fluids. Such newly formed fluids would interact with a primary pegmatite matrix along the fractures and cause autometasomatic alteration, recrystallization, leaching and formation of “primary–secondary” pockets. 相似文献
17.
Crystallization experiments have been conducted in the system Na 2O–K 2O–MgO–FeO–Al 2O 3–SiO 2–H 2O (with 4% normative corundum) in order to constrain the stability of biotite as a function of water activity and the Mg# of biotite [Mg/(Mg +Fe total)] in equilibrium with peraluminous granitic melts. The temperature at which biotite breakdown starts is strongly dependent on the Mg# of biotite. At 500 MPa, the temperature of biotite breakdown to form orthopyroxene increases from 750 °C to 830 °C, as the Mg# of biotite increases from 0.4 to 0.5. Considering that the system investigated is relevant for Ca-poor peraluminous biotite-bearing rocks (metapelites), the biotite dehydration curves obtained are used to discuss the melting reactions and the temperatures that lead to the formation of two distinct types of two-mica granites found in the South Bohemian batholith (specifically the Eisgarn and Deštná granites). The phase relationships were determined experimentally for the composition of these two granites in order to constrain the composition of the biotite in equilibrium with the melt in the protoliths. We demonstrate that Eisgarn granitic melts may have been generated at temperatures in the range 830–850 °C from melting reactions involving biotite with a Mg# up to 0.5 as a reactant. In contrast, Deštná granitic melts cannot have been generated from dehydration melting reactions involving biotite. 相似文献
18.
Experimental studies of synthetic and natural basalt systems suggest that conditions of magma genesis and fractionation depend fundamentally on mantle temperatures and lithospheric stress fields. In general, compressional settings are more conducive to polybaric fractionation than extensional settings and in this regard, the Anatolian magmatic province offers a natural laboratory for comparing near-coeval basalt eruptions as a function of regional tectonics — compressional (collision-related) régimes dominating in eastern Anatolia and extensional tectonics characterizing a western province related to Aegean Sea opening. Projection of Plio-Quaternary basalt normative compositions from the Western Anatolia Extensional Province (WAEP), the Central Anatolian ‘Ova’ Province (CAOP), and Eastern Anatolia Compressional Province (EACP) are projected onto Ol–Ne–Cpx and Pl–Cpx–Ol planes in the simplified basalt system (Ne–Cpx–Ol–Qz), each showing distinctive liquid lines of descent. WAEP basalts are mostly constrained by low-pressure (< 0.5 GPa) cotectics while CAOP and EACP compositions conform to moderate and/or high-pressure (0.8–3.0 GPa) cotectics. Overall, a quasi-linear shift from moderate and/or high-pressure to low-pressure equilibria matches the westward transgression from compressional east Anatolia to the extensional west Anatolian–Aegean region. Comparison of their respective primary (mantle-equilibrated) magmas–simulated by normalizing their compositions to MgO = 15 wt.% (Mg-15)–with parameterized anhydrous and H 2O-undersaturated experimental melts suggests they segregated from spinel- to garnet-lherzolite mantle facies at pressures between c. 2 and 3 GPa (c. 70–100 km depth) under H 2O-undersaturated conditions. Interpolated potential temperatures ( Tp) and lithospheric stretching factors ( β) range as follows: (1) eastern Anatolian basalts associated with the Arabian foreland show Tp varying between 1250 and 1400 °C (except for the Karacalidag alkali basalts, south of the Bitlis–Zagros fracture zone, for which Tp ranges up to 1450 °C), for β values of 1.2–1.8. Tp values for central Anatolia (e.g. Sivas) range between 1300 and 1375 °C (except for Karapinar, Egrikuyu and Hasandag, which show < 1150 °C), and β values of 1.3–1.4. For western Anatolian basalts, Tp range mostly between 1250 and 1330 °C, except for a single value for Canakkale of 1400 °C and Kula sample showing Tp < 1200 °C, and β values of 1.3–2.0. Variation of these conditions is as great or greater than that between provinces, although there are clearly significant constraints on the inferred polybaric to low-pressure isobaric fractionation régimes. Covariation of total FeO, TiO 2, La/Yb, Ce/Sm, Zr/Y and Zr/Nb reflects small but significant differences in bulk composition and ambient melt fraction while the covariance of Ce/Sm and Sm/Yb is consistent with the segregation of primitive melts at the spinel- to garnet-lherzolite transition. 相似文献
19.
Strongly peraluminous (SP) granites have formed as a result of post-collisional processes in various orogens. In ‘high-pressure' collisions such as the European Alps and Himalayas, post-collisional exhumation of overthickened crust (>50 km), heated by radiogenic decay of K, U and Th during syn-collisional thickening, produced small- to moderate-volume, cool (<875°C) SP granite melts with high Al 2O 3/TiO 2 ratios. In ‘high-temperature' collisions such as the Hercynides and Lachlan Fold Belt (LFB), there was less syn-collisional crustal thickening (≤50 km). Crustal anatexis was related to post-collisional lithospheric delamination and upwelling of hot asthenosphere, forming large-volume, hot (≥875°C) SP granite melts with low Al 2O 3/TiO 2 ratios. Both clay-rich, plagioclase-poor (<5%) pelitic rocks and clay-poor, plagioclase-rich (>25%) psammitic rocks have been partially melted in high-pressure and high-temperature collisional orogens, with the pelite-derived SP granites tending to have lower CaO/Na 2O ratios (<0.3) than their psammite-derived counterparts. The predominance of pelite-derived SP granites in the Himalayas and psammite-derived SP granites in the LFB suggests that mature continental platforms made up more of the accreted crust in the Himalayan collision than in the LFB. 相似文献
20.
鄂尔多斯西南缘地处北秦岭、北祁连、贺兰山构造带交接部位,构造带西段的南华山弧形构造带中发育有大量早古生代花岗岩体（岩株）,侵入于下元古界海原群以及中寒武统香山群、下奥陶统阴沟群中。岩性以花岗闪长岩为主,其次为二长花岗岩和石英闪长岩,并有少量角闪奥长花岗岩和斑状花岗岩等,其中普遍含有暗色闪长质包体。地球化学研究表明,岩石主要为准铝-过铝质、钙碱性系列,具有明显高Al 2O 3、低MgO特征,尤其是低Y和Yb、高Sr和Sr/Y比值特征,类似于典型的埃达克岩地球化学组成。同时,岩石明显亏损Nb、Ta、P 和Ti,富集Cs、Rb、Ba、Th、U、K、Pb、Nd、Zr 等。综合分析认为,早古生代祁连俯冲洋壳板片熔融,熔体与楔形地幔熔体混合后上侵,并与下地壳熔体再次混合形成了南华山花岗岩。利用LA-ICPMS法测得花岗岩锆石U-Pb同位素年龄为416±14 Ma,代表了花岗岩结晶年龄。综合利用区域地质、地层特征和不整合接触关系,限定祁连-秦岭交接区俯冲、碰撞造山和地壳加厚发生在志留纪末期。 相似文献
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