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1.
The upper greenschist - lower amphibolite facies, argillaceous to chemical-exhalative metasedimentary sequence of the Mesoarchaean Ghattihosahalli Schist Belt (GHSB), southern India, has been examined with a special focus on the paragenesis and solid solution characteristics of barian feldspars and associated dioctahedral Ba-Cr-bearing micas. Barian feldspars occur as untwinned porphyroblasts in a recrystallized finely banded matrix of barite, quartz and minor white mica. Idioblastic celsian (Cls98-76Or2-20Ab1-8) and hyalophane (Cls55-39Or35-51Ab10) predate the greenschist-facies foliation, whereas xenoblastic hyalophane (Cls44-35Or45-59Ab8–17) and mantles on celsian (Cls45-35Or42-60Ab13-5) as well as xenoblastic barian K-feldspar (Cls6Or90Ab2) postdate the last fabric-defining event. The preservation of extremely complex zoning patterns down to the micron-scale shows that diffusional homogenization did not operate at fluid-present low to medium-grade conditions (350–550 °C, 3–5 kb). Microstructures indicate that at these conditions barian feldspars deform exclusively by brittle fracturing and do not undergo recrystallization. Barian feldspar compositions confirm the positive correlation of Na-content with temperature and the existence of a narrow asymmetric compositional gap (Cls90-85?Cls55, ~350 °C) which probably closes at lower amphibolite facies conditions (Xc ~Cls75; Tc ~550 °C). White micas are solid solutions of the end-members muscovite, ganterite (Ba0.5?K0.5)Al2(Al1.5Si2.5)O10(OH)2, paragonite, celadonite with a significant substitution of [VI]Al by Cr. Zoning is a common feature with cores being enriched in Ba. The data document extensive Ba substitution for K from muscovite to ganterite, exclusively controlled by the coupled substitution [XII]K + [IV]Si ? [XII]Ba + [IV]Al and strongly dependent on bulk composition. The extent of solid solution from (Ms+Gnt) towards paragonite and celadonite end-members is controlled by the miscibility gap in the (Ms+Gnt)–Pg–Cel pseudoternary, with the Pg-substitution depending on temperature and the Cel-substitution on pressure. [IV]Si values between 3.1 and 3.3 in Ba-poor micas indicate minimum pressures of chemical equilibration in the order of 3–5 kbar, while the most sodian compositions of low-celadonite micas provide an upper temperature estimate of ~550 °C, consistent with P-T estimates for assemblages of metapelites (500–550 °C, 4–5 kb).  相似文献   

2.
Subsolidus phase relations for a K-doped lherzolite are investigated in the model system K2O–Na2O–CaO–FeO–MgO–Al2O3–SiO2–H2O at 1.5–6.0 GPa and 680–1,000°C. Phlogopite is ubiquitous and coexists with Ca-amphibole up to 3.2 GPa and 900°C. High-pressure phlogopites show a peculiar mineral chemistry dependent on pressure: e.g., at 5.5 GPa and 680°C, excess of Si (up to 3.4 apfu) coupled with deficiency in Al (as low as 0.58 apfu) and K + Na (as low as 0.97 apfu), suggest a significant amount of a talc/10 Å phase component ([v]XIISi1K?1Al ?1 IV , where [v]XII is interlayer vacancy). Mixed layering or solid solution relations between high-pressure phlogopites and the 10 Å phase, Mg3Si4O10(OH)2 nH2O, are envisaged. Phlogopite modal abundance, derived by weighted least squares, is maximum at high-pressure and relative low-temperature conditions and therefore along the slab–mantle interface (10.3 ± 0.7 wt.%, at 4.8 GPa, 680°C). In phlogopite-bearing systems, Ca-amphibole breaks down between 2.5 and 3.0 GPa, and 1,000°C, through the water conservative reaction 5(pa + 0.2 KNa?1) + 17en + 15phl = (10di + 4jd) + 5py + 12fo + 20(phl + 0.2 talc), governed by bulk composition and pressure-dependent variations of K/OH in K-bearing phases and as a result, it does not necessarily imply a release of fluid.  相似文献   

3.
Phase relations for the bulk compositions of the celadonites between the MgAl, MgFe3+ and Fe2+Fe3+ types (celadonite = KR2+R3+ Si4O10 (OH)2) under magnetite-iron and nickel-nickel oxide solid-fluid buffers indicate the extent of solid solution possible in this potassic mica series at temperatures between 300° and 430° C at 2 Kb total pressure. Other possible combinations of Mg, Al, Fe ions in octahedrally coordinated sites did not produce single-phase mica products. The ferrous celadonite micas are stable only under oxygen fugacities where magnetite is the stable oxide—where both Fe2+ and Fe3+ can coexist. However the celadonite with the highest thermal stability at 2 Kb total pressure, nickel-nickel oxide buffer conditions is the KMgFe3+Si4O10(OH)2 phase which is stable up to 420°C, well into low grade metamorphic conditions. It is thus apparent that the presence of celadonite or glauconite mica will not be indicative of changing diagenetic conditions.  相似文献   

4.
Ultrahigh‐pressure (UHP) rocks from the Western Gneiss Region (WGR) of Norway record subduction of Baltican continental crust during the Silurian to Devonian Scandian continental collision. Here, we report a new coesite locality from the island of Harøya in the Nordøyane UHP domain, the most northerly yet documented in the WGR, and reconstruct the P–T history of the host eclogite. The coesite–eclogite lies within migmatitic orthogneiss, interpreted as Baltica basement, that underwent multiple stages of deformation and partial melting during exhumation. Two stages of metamorphism have been deduced from petrography and mineral chemistry. The early (M1) assemblage comprises garnet (Pyr38–41Alm35–37Grs23–26Spss1) and omphacite (Na0.35–0.40Ca0.57–0.60Fe2+0.08–0.10Mg0.53Fe3+0.01AlVI0.40–0.42)2(AlIV0.03–0.06Si1.94–1.97)2O6, with subordinate phengite, kyanite, rutile, coesite and apatite, all present as inclusions in garnet. The later (M2) assemblage comprises retrograde rims on garnet (Pyr38–40Alm40–44Grs16–21Spss1), diopside rims on omphacite (Na0.04–0.06Ca0.88–0.91Fe2+0.09–0.13Mg0.81–83Fe3+0.08AlVI0.03)2(AlIV0.07–0.08Si1.92–1.93)2O6, plagioclase, biotite, pargasite, orthopyroxene and ilmenite. Metamorphic P–T conditions estimated using thermocalc are ～3 GPa and 760 °C for M1, consistent with the presence of coesite, and ～1 GPa and 813 °C for M2, consistent with possible phengite dehydration melting during decompression. Comparison with other WGR eclogites containing the same assemblage shows a broad similarity in peak (M1) P–T conditions, confirming suggestions that large portions of the WGR were buried to depths of ～100 km during Scandian subduction. Field relations suggest that exhumation, accompanied by widespread partial melting, involved an early phase of top‐northwest shearing, followed by subhorizontal sinistral shearing along northwest‐dipping foliations, related to regional transtension. The present results add to the growing body of data on the distribution, maximum P–T conditions, and exhumation paths of WGR coesite–eclogites and their host rocks that is required to constrain quantitative models for the formation and exhumation of UHP metamorphic rocks during the Scandian collision.  相似文献   

5.
The solubility of the albite-paragonite-quartz mineral assemblage was measured as a function of NaCl and fluorine concentration at 400°C, 500 bars and at 450°C, 500 and 1000 bars. Decreasing Al concentrations with increasing NaCl molality in F-free fluids of low salinity (mNaCl < 0.01) demonstrates that Al(OH)4− dominates Al speciation and is formed according to the reaction 0.5 NaAl3Si3O12H2(cr)+2 H2O = 0.5 NaAlSi3O8(cr)+Al(OH)4−+H+. Log K results for this reaction are −11.28 ± 0.10 and −10.59 ± 0.10 at 400°C, 500 bars and 450°C, 1000 bars, respectively. Upon further salinity increase, Al concentration becomes constant (at 400°C, 500 bars) or even rises (at 450°C, 1000 bars). The observed Al behavior can be explained by the formation of NaAl(OH)40(aq) or NaAl(OH)3Cl(aq)0. The calculated constant for the reaction Al(OH)4−+Na+=NaAl(OH)40(aq) expressed in log units is equal to 2.46 and 2.04 at 400°C, 500 bars and 450°C, 1000 bars, respectively. These values are in good agreement with the predictions given in Diakonov et al. (1996). Addition of fluoride at m(NaCl) = const = 0.5 caused a sharp increase in Al concentration in equilibrium with the albite-paragonite-quartz mineral assemblage. As fluid pH was also constant, this solubility increase indicates strong aluminum-fluoride complexation with the formation of NaAl(OH)3F(aq)0 and NaAl(OH)2F20(aq), according to 0.5 NaAl3Si3O12H2(cr)+Na++HF(aq)0+H2O = 0.5 NaAlSi3O8(cr)+ NaAl(OH)3F(aq)0+H+, log K = −5.17 and −5.23 at 400°C and 450°C, 500 bars, respectively, and 0.5 NaAl3Si3O12H2(cr)+Na++2 HF(aq)0 = 0.5 NaAlSi3O8(cr)+NaAl(OH)2F20(aq)+H+, log K = −2.19 and −1.64 at the same P-T conditions. It was found that temperature increase and pressure decrease promote the formation of Na-Al-OH-F species. Stability of NaAl(OH)2F20(aq) in low-density fluids also increases relative to NaAl(OH)3F(aq)0. These complexes, together with Al(OH)2F(aq)0 and AlOHF20(aq), whose stability constants were calculated from the corundum solubility measured by Soboleva and Zaraisky (1990) and Zaraisky (1994), are likely to dominate Al speciation in metamorphic fluids containing several ppm of fluorine.  相似文献   

6.
Garnet peridotites occur in quartzofeldspathic gneisses in the Northern Qaidam Mountains, western China. They are rich in Mg and Cr, with mineral compositions similar to those in mantle peridotites found in other orogenic belts and as xenoliths in kimberlite. Garnet‐bearing lherzolites interlayered with dunite display oriented ilmenite and chromite lamellae in olivine and pyroxene lamellae in garnet that have been interpreted to indicate pressures in excess of 6 GPa. However, some garnet porphyroblasts include hornblende, chlorite and spinel + orthopyroxene symplectite after garnet; some clinopyroxene porphyroblasts include abundant actinolite/edenite, calcite and lizardite in the lherzolite; some olivine porphyroblasts (Fo92) include an earlier generation Mg‐rich olivine (Fo95–99), F‐rich clinohumite, pyroxene, chromite, anthophyllite/cummingtonite, Cl‐rich lizardite, carbonates and a new type of brittle mica, here termed ‘Ca‐phlogopite’, in the associated dunite. The pyrope content of garnet increases from core to rim, reaching the pyrope content (72 mol.%) of garnet typically found in the xenoliths in kimberlite. The simplest interpretation of these observations is that the rock association was formerly mantle peridotite emplaced into the oceanic crust that was subjected to serpentinization by seawater‐derived fluids near the sea floor. Dehydration during subduction to 3.0–3.5 GPa and 700 °C transformed these serpentinites into garnet lherzolite and dunite, depending on their Al and Ca contents. Pseudosection modelling using thermocalc shows that dehydration of the serpentinites is progressive, and involved three stages for Al‐rich and two stages for Al‐poor serpentinites, corresponding to the breakdown of the key hydrous minerals. Static burial and exhumation make olivine a pressure vessel for the pre‐subduction mineral inclusions during ultrahigh‐pressure (UHP) metamorphism. The time span of the UHP event is constrained by the clear interface between the two generations of olivine to be very short, implying rapid subduction and exhumation.  相似文献   

7.
In the oxidation zone of the Berezovskoe gold deposit in the middle Urals, Russia, minerals of the beudantite–segnitite series (idealized formulas PbFe3 3+ AsO4)(SO4)(OH)6 and PbFe3 3+ AsO4)(AsO3OH)(OH)6, respectively) form a multicomponent solid solution system with wide variations in the As, S, Fe, Cu, and Sb contents and less variable P, Cr, Zn, Pb, and contents K. The found minerals of this system correspond to series from beudantite with 1.25 S apfu to S-free segnitite, with segnitite lacking between 1.57 and 1.79 As apfu. Segnitite at the Berezovskoe deposit contains presumably pentavalent Sb (up to 15.2 wt % Sb2O5 = 0.76 Sb apfu, the highest Sb content in the alunite supergroup minerals), which replaces Fe3+. The Sb content increases with increasing As/S value. On the contrary, beudantite is free of or very poor in Sb (0.00–0.03 Sb apfu). Many samples of segnitite are enriched in Cu (up to 8.2 wt% CuO = 0.83 Cu apfu, uncommonly high Cu content for this mineral) and/or in Zn (up to 2.0 wt% ZnO = 0.19 Zn apfu). Both Cu and Zn replace Fe. The generalized formula of a hypothetic end member of the segnitite series with 1 Sb apfu is Pb(Fe3+ M 2+Sb5+)(AsO4)2(OH)6, where M = Cu, Zn, Fe2+. The chemical evolution of beudantite–segnitite series minerals at the Berezovskoe deposit is characterized by an increase in the S/As value with a decrease in the Sb content from early to late generations.  相似文献   

8.
 Amphiboles were synthesized from bulk compositions prepared along the join Ca1.8Mg5.2Si8O22(OH)2–Ca1.8Mg3Ga4Si6O22(OH)2 hydrothermally at 750–850 °C and 1.0–1.8 GPa, and along the join Ca2Mg5Si8O22F2–Ca2Mg3Ga4Si6O22F2, anhydrously at 1000 °C and 0.7 GPa to document how closely the tschermak-type substitution is obeyed in these analogues of aluminous amphiboles. Electron-microprobe analyses and Rietveld X-ray diffraction structure refinements were performed to determine cation site occupancies. The extent of Ga substitution was found to be limited in both joins, but with the fluorine series having about twice the Ga content (0.6 atoms per formula unit, apfu) of the hydroxyl-series amphiboles (0.3 apfu). The tschermak-type substitution was followed very closely in the hydroxyl series with essentially equal partitioning of Ga between tetrahedral and octahedral sites. The fluorine-series amphiboles deviated significantly from the tschermak-type substitution and, instead, appeared to follow a substitution that is close to a Ca-pargasite substitution of the type: [6]Ga3++2[4]Ga3++1/2[A] Ca2+ = [6]Mg2++2[4]Si4++1/2[A]□. Infrared spectroscopy revealed an inverse correlation between the intensity of the OH-stretching bands and the Ga content for the hydroxyl- and fluorine-series amphiboles. The direct correlation between the Ga and F content and inverse relationship between the Ga and OH content may be a general phenomenon present in other minerals and suggests, for example, that high F contents in titanite are controlled by the Al content of the host rock and that there may be similar direct Al–F correlations in tschermakitic amphiboles. Evidence for the possibility that Al (Ga) might substitute onto only a subset of the tetrahedral sites in tschermakitic amphiboles was sought but not observed in this study. Received: 5 March 2001 / Accepted: 31 July 2001  相似文献   

9.
The solubility of Tio2 in phlogopites has been experimentally determined in the system K2Mg6Al2Si6O20(OH)4-K2Mg4TiAl2Si6O20(OH)4-K2Mg5TiAl4Si4O20(OH)4 between 825–1300°C and 10–30 kbar under vapour absent conditions. Starting compositions lie along the join K2Mg6Al2Si6O20(OH)4-K2Mg4.5TiAl3Si5O20(OH)4 which represents a combination of the Mg[VI]2Si[IV] = Ti[VI]2Al[VI] and 2Mg[VI] = Ti[VI]□[VI] substitution mechanisms for Ti in phlogopites. The results of the experiments indicate a systematic increase in solubility of Ti with increasing temperature and decreasing pressure for given bulk Tio2 content. Under isobaric conditions high temperature Ti-saturated phlogopite breaks down to Ti-deficient phlogopite + rutile + vapour. Mass balance calculations suggest that the vapour phase may contain K2O dissolved in H2O and that the reaction is controlled by the vapour phase. Analyses of phlogopites coexisting with rutile and vapour can be represented in terms of the end-member components phlogopite [K2Mg6Al2Si6O20(OH)4], eastonite [K2Mg5Al4Si5O20(OH)4], an octahedral site deficient Ti-phlogopite (Ti-OSD) of composition K2(Mg4Ti□)Al2Si6)O20(OH)4, and Ti-eastonite [K2Mg5TiAl4Si4O20(OH)4]. With decreasing amounts of Ti in these phlogopites there is a decrease in the Ti-eastonite component and increase in the eastonite component.The general equation for the breakdown of Ti-phlogopite solid solution to Ti-free phlogopite + rutile + vapour is: 14 Ti-eastonite + 7 Ti-OSD ? 16 eastonite + 3 phlogopite + 21 rutile + 4 H2O + 2 K2O. Lack of knowledge of H2O and K2O activities in the vapour phase does not permit evaluation of thermodynamic constants for this reaction. The Ti solubility in phlogopites and hence its potential as a geothermobarometer under lower crustal to upper mantle conditions is likely controlled by common mantle minerals such as forsterite.  相似文献   

10.
Germanate garnets are often used as isostructural analogues of silicate garnets to provide insight into the crystal chemistry and symmetry of the less accessible natural garnet solid solutions. We synthesised two series of germanate garnets at 3 GPa along the joinVIIICa3VI(CaGe)IVGe3O12–VIIICa3VIFe2IVGe3O12 at 900 °C and 1,100 °C. Samples with compositions close to the CaGeO3 end-member consist of tetragonal garnet with a small amount of triclinic CaGe2O5. Samples with nominal compositions between XFe=0.4 and 1.0 consist of a mixture of tetragonal and cubic garnets; whereas, single-phase cubic garnets were obtained for compositions with XFe>1.2 (XFe gives the iron content expressed in atoms per formula unit, and varies between 0 and 2 along the join). Run products which were primarily single-phase garnet were investigated using Mössbauer spectroscopy. Spectra from samples synthesised at 1,100°C consist of one well-resolved doublet that can be assigned to Fe3+ in the octahedral site of the garnet structure. A second doublet, present primarily in samples synthesised at 900°C, can be assigned to Fe2+ at the octahedral sites of the garnet structure. The relative abundance of Fe2+ decreases with increasing iron content. Transmission electron microscopy analyses confirm this tendency and show that the garnets are essentially defect-free. The unit-cell parameters of tetragonal VIIICa3VI(CaGe)IVGe3O3 garnet decrease with increasing synthesis temperature, and the deviation from cubic symmetry becomes smaller. Cubic garnets show a linear decrease of unit-cell parameter with increasing iron content. The results are discussed in the context of iron incorporation into VIIIMg3VI(MgSi)IVSi3O3 majorite.  相似文献   

11.
Si+4 Content of natural phengites   总被引：2，自引：0，他引：2  
The chemical compositions of white micas separated from adjacent rocks of glaucophane and greenschist facies are compared with respect to their Si+4 content. The micas are predominantly phengitic, i.e. between muscovite, K[Al2Si3AlO10(OH)2] and celadonite, K[(R+2R+3)Si4O10(OH)2] in composition. Constancy of Si content in micas coming from rocks of different bulk chemical composition but closely similar physical conditions indicates that the silica content of a potassic dioctahedral mica can be used to indicate the pressure and temperature conditions of its formation. This conclusion is in part based upon previous experimental data obtained for synthetic phengites.  相似文献   

12.
Garnets in UHP eclogites from Bixiling in Dabieshan were investigated by Fourier transform infrared spectroscopy (FTIR). The results indicate that all garnets contain structural water that occurs as hydroxyl (OH−) and non-structural molecular water (H2O) possibly in the form of sub-microscopic fluid inclusions. The structural hydroxyl contents range from 92 to 1735 ppm (H2O wt.) and most are between 200 and 1000 ppm. Therefore, garnet in eclogite can recycle surface water into the mantle. Various water contents were observed among different samples of the same outcrop (∼150 m) and in different domains of the same sample (∼1 cm). This variability in structural H2O contents suggests that the mobility of fluids during UHP metamorphism was very limited, and that both subduction and exhumation processes of UHP rocks occurred in a short time interval.  相似文献   

13.
Mineral inclusions in pyrope crystals from Garnet Ridge in the Navajo Volcanic Field on the Colorado Plateau are investigated in this study with emphasis on the oxide minerals. Each pyrope crystal is roughly uniform in composition except for diffusion halos surrounding some inclusions. The pyrope crystals have near constant Ca:Fe:Mg ratios, 0.3 to 5.7 wt% Cr2O3, and 20 to 220 ppm H2O. Thermobarometric calculations show that pyrope crystals with different Cr contents formed at different depths ranging from 50 km (where T ≈ 600 °C and P = 15 kbar) to 95 km (where T ≈ 800 °C and P = 30 kbar) along the local geotherm. In addition to previously reported inclusions of rutile, spinel and ilmenite, we discovered crichtonite series minerals (AM21O38, where A = Sr, Ca, Ba and LREE, and M mainly includes Ti, Cr, Fe and Zr), srilankite (ZrTi2O6), and a new oxide mineral, carmichaelite (MO2−x(OH)x, where M = Ti, Cr, Fe, Al and Mg). Relatively large rutile inclusions contain a significant Nb (up to 2.7 wt% Nb2O5), Cr (up to ∼6 wt% Cr2O3), and OH (up to ∼0.9 wt% H2O). The Cr and OH contents of rutile inclusions are positively related to those of pyrope hosts, respectively. Needle- and blade-like oxide inclusions are commonly preferentially oriented. Composite inclusions consisting mainly of carbonate, amphibole, phlogopite, chlorapatite, spinel and rutile are interpreted to have crystallized from trapped fluid/melt. These minerals in composite inclusions commonly occur at the boundaries between garnet host and large silicate inclusions of peridotitic origin, such as olivine, enstatite and diopside. The Ti-rich oxide minerals may constitute a potential repository for high field strength elements (HFSE), large ion lithophile elements and light rare earth elements (LREE) in the upper mantle. The composite and exotic oxide inclusions strongly suggest an episode of metasomatism in the depleted upper mantle beneath the Colorado Plateau, contemporaneous with the formation of pyrope crystals. Our observations show that mantle metasomatism may deplete HFSE in metasomatic fluids/melts. Such fluids/melts may subsequently contribute substantial trace elements to island arc basalts, providing a possible mechanism for HFSE depletion in these rocks. Received: 20 December 1997 / Accepted: 15 October 1998  相似文献   

14.
Some of the most vanadium-rich silicate minerals known are present in green mica schist from the Hemlo gold deposit, Ontario, Canada. Vanadium-rich silicate minerals include green mica (up to 17.6 wt. % V2O3), phlogopite (10.1 wt. % V2O3), pumpellyite (25.7 wt. % V2O3), garnet (18.5 wt. % V2O3), epidote-group minerals (9.1 wt. % V2O3), antimonian vesuvianite (4.3 wt. % V2O3), and titanite (18.5 wt. % V2O5). In addition, minor amounts of V (<2 wt. % V2O3) are present in tourmaline, chlorite, talc and tremolite in other lithologies of the Hemlo deposit. The principal substitution that incorporates V into most of these silicate minerals is Al3+=V3+ in octahedral positions. Vanadium is incorporated into phlogopite mainly by the two substitutions: 3Mg2+ =2V3++ and VIMg2++IVSi4+=VIV3+ +IVAl3+, and all of the three substitutions Ti4++O2- =V3++(OH,F)-, Ti4+=V4+, and 5Ti4+=4V5+ + may have operated in titanite.Vanadium-enriched green mica schist from the Hemlo gold deposit is characterized by uniform Ti/Zr ratios, systematically low Ti, Ni, Co and Sc abundances, and low levels of incompatible elements Th, U, Hf and Zr and is distinct in these respects from its Cr-enriched counterpart. These geochemical features, along with textural evidence (relict quartz and oligoclase phenocrysts), indicate that the V-enriched green mica schist from Hemlo was most likely derived mainly from quartz-oligoclase porphyry. However, its anomalously high V and Cr contents were probably introduced metasomatically from local maficultramafic sources and were fixed in green mica and oxides during the waning of a second regional metamorphism. Vanadium was further remobilized, and its concentration probably enhanced, during the late hydrothermal alteration, which resulted in the formation of the characteristic V-rich calc-silicate minerals.  相似文献   

15.
Summary The phase relations of K-richterite, KNaCaMg5Si8O22(OH)2, and phlogopite, K3Mg6 Al2Si6O20(OH)2, have been investigated at pressures of 5–15 GPa and temperatures of 1000–1500 °C. K-richterite is stable to about 1450 °C at 9–10 GPa, where the dp/dT-slope of the decomposition curve changes from positive to negative. At 1000 °C the alkali-rich, low-Al amphibole is stable to more than 14 GPa. Phlogopite has a more limited stability range with a maximum thermal stability limit of 1350 °C at 4–5 GPa and a pressure stability limit of 9–10 GPa at 1000 °C. The high-pressure decomposition reactions for both of the phases produce relatively small amounts of highly alkaline water-dominated fluids, in combination with mineral assemblages that are relatively close to the decomposing hydrous phase in bulk composition. In contrast, the incongruent melting of K-richterite and phlogopite in the 1–3 GPa range involves a larger proportion of hydrous silicate melts. The K-richterite breakdown produces high-Ca pyroxene and orthoenstatite or clinoenstatite at all pressures above 4 GPa. At higher pressures additional phases are: wadeite-structured K2SiVISiIV 3O9 at 10 GPa and 1500 °C, wadeite-structured K2SiVISiIV 3O9 and phase X at 15 GPa and 1500 °C, and stishovite at 15 GPa and 1100 °C. The solid breakdown phases of phlogopite are dominated by pyrope and forsterite. At 9–10 GPa and 1100–1400 °C phase X is an additional phase, partly accompanied by clinoenstatite close to the decomposition curve. Phase X has variable composition. In the KCMSH-system (K2CaMg5Si8O22(OH)2) investigated by Inoue et al. (1998) and in the KMASH-system investigated in this report the compositions are approximately K4Mg8Si8O25(OH)2 and K3.7Mg7.4Al0.6Si8.0O25(OH)2, respectively. Observations from natural compositions and from the phlogopite-diopside system indicate that phlogopite-clinopyroxene assemblages are stable along common geothermal gradients (including subduction zones) to 8–9 GPa and are replaced by K-richterite at higher pressures. The stability relations of the pure end member phases of K-richterite and phlogopite are consistent with these observations, suggesting that K-richterite may be stable into the mantle transition zone, at least along colder slab geotherms. The breakdown of moderate proportions of K-richterite in peridotite in the upper part of the transition zone may be accompanied by the formation of the potassic and hydrous phase X. Additional hydrogen released by this breakdown may dissolve in wadsleyite. Therefore, very small amounts of hydrous fluids may be released during such a decomposition. Received April 10, 2000; revised version accepted November 6, 2000  相似文献   

16.
A geochemical study of pegmatitic micas from Minas Gerais State in Brazil was performed with an electron microprobe, in order to examine the variations of Rb, K, Al and F contents. It is observed a linear decreasing relationship between the [Rb/K] ratio of the micas and their contents in AlVI. The interpretation is based on the hypothesis that the partition coefficient CRb/Kmica/fl between fluid and mineral does not vary significantly as a function of temperature and pressure in the narrow conditions of crystallization of pegmatites. It is suggested that the relation: CRb/Kmica/fl=0.55×(5?[AlVI]) is of crystallochemical order. Micas with low contents in Al take higher contents in Rb because the potassic sites where Rb enters are larger. This relation gives another way of calculating the values [Rb/K] of the fluids knowing Rb, K, Al and Si in the micas. This crystallochemistry also allows us to foresee a direct correlation between Rb and F in the pegmatitic micas. To cite this article: J. Quéméneur et al., C. R. Geoscience 336 (2004).  相似文献   

17.
Sodic amphiboles in high pressure and ultra-high pressure (UHP) metamorphic rocks are complex solid solutions in the system Na2O–MgO–Al2O3–SiO2–H2O (NMASH) whose compositions vary with pressure and temperature. We conducted piston-cylinder experiments at 20–30?kbar and 700–800?°C to investigate the stability and compositional variations of sodic amphiboles, based on the reaction glaucophane=2jadeite+talc, by using the starting assemblage of natural glaucophane, talc and quartz, with synthetic jadeite. A close approach to equilibrium was achieved by performing compositional reversals, by evaluating compositional changes with time, and by suppressing the formation of Na-phyllosilicates. STEM observations show that the abundance of wide-chain structures in the synthetic amphiboles is low. An important feature of sodic amphibole in the NMASH system is that the assemblage jadeite–talc?±?quartz does not fix its composition at glaucophane. This is because other amphibole species such as cummingtonite (Cm), nyböite (Nyb), Al–Na-cummingtonite (Al–Na-Cm) and sodium anthophyllite (Na-Anth) are also buffered via the model reactions: 3cummingtonite?+?4quartz?+?4H2O=7talc, nyböite?+?3quartz=3jadeite?+?talc, 3Al–Na-cummingtonite + 11quartz + 2H2O=6jadeite + 5talc, and 3 sodium anthophyllite?+?13quartz?+?4H2O=3 jadeite + 7talc. We observed that at all pressures and temperatures investigated, the compositions of newly grown amphiboles deviate significantly from stoichiometric glaucophane due to varying substitutions of AlIV for Si, Mg on the M(4) site, and Na on the A-site. The deviation can be described chiefly by two compositional vectors: [NaAAlIV]<=>[□ASi] (edenite) toward nyböite, and [Na(M4)AlVI]<=>[Mg(M4)MgVI] toward cummingtonite. The extent of nyböite and cummingtonite substitution increases with temperature and decreases with pressure in the experiments. Similar compositional variations occur in sodic amphiboles from UHP rocks. The experimentally calibrated compositional changes therefore may prove useful for thermobarometric applications.  相似文献   

18.
We report the first finding of diamond and moissanite in metasedimentary crustal rocks of Pohorje Mountains (Slovenia) in the Austroalpine ultrahigh‐pressure (UHP) metamorphic terrane of the Eastern Alps. Microscopic observations and Raman spectroscopy show that diamond occurs in situ as inclusions in garnet, being heterogeneously distributed. Under the optical microscope, diamond‐bearing inclusions are of cuboidal to rounded shape and of pinkish, yellow to brownish colour. The Raman spectra of the investigated diamond show a sharp, first order peak of sp3‐bonded carbon, in most cases centred between 1332 and 1330 cm?1, with a full width at half maximum between 3 and 5 cm?1. Several spectra show Raman bands typical for disordered graphitic (sp2‐bonded) carbon. Detailed observations show that diamond occurs either as a monomineralic, single‐crystal inclusion or it is associated with SiC (moissanite), CO2 and CH4 in polyphase inclusions. This rare record of diamond occurring with moissanite as fluid‐inclusion daughter minerals implies the crystallization of diamond and moissanite from a supercritical fluid at reducing conditions. Thermodynamic modelling suggests that diamond‐bearing gneisses attained P–T conditions of ≥3.5 GPa and 800–850 °C, similar to eclogites and garnet peridotites. We argue that diamond formed when carbonaceous sediment underwent UHP metamorphism at mantle depth exceeding 100 km during continental subduction in the Late Cretaceous (c. 95–92 Ma). The finding of diamond confirms UHP metamorphism in the Pohorje Mountains, the most deeply subducted part of Austroalpine units.  相似文献   

19.
Several types of multiphase solid (MS) inclusions are identified in garnet from ultrahigh‐pressure (UHP) eclogite in the Dabie orogen. The mineralogy of MS inclusions ranges from pure K‐feldspar to pure quartz, with predominance of intermediate types consisting of K‐feldspar + quartz ± silicate (plagioclase or epidote) ± barite. The typical MS inclusions are usually surrounded with radial cracks in the host garnet, similar to where garnet contains relict coesite. Barite aggregates display significant heterogeneity in major element composition, with total contents of only 57–73% and highly variable SiO2 contents of 0.32–25.85% that are positively correlated with BaO and SO3 contents. The occurrence of MS inclusions provides petrographic evidence for partial melting in the UHP metamorphic rock. The occurrence of barite aggregates with variably high SiO2 contents suggests the coexistence of aqueous fluid with hydrous melt under HP eclogite facies conditions. Thus, local dehydration melting is inferred to take place inside the UHP metamorphic slice during continental collision. This is ascribed to phengite breakdown during ‘hot’ exhumation of the deeply subducted continental crust. As a consequence, the aqueous fluid is internally buffered in chemical composition and its local sink is a basic trigger to the partial melting during the continental subduction‐zone metamorphism.  相似文献   

20.
The partitioning of Fe and Mn between the large M(4) site and the octahedral sites, M(1,2,3) in the amphibole structure has been investigated in two natural manganogrunerites of compositions Ca0.1Mn1.9 Mg1.25Fe2+ 3.56Fe3+ 0.38Si7.81O22(OH)2 and Ca0.24Mn1.57 Mg2.27 Fe2+ 2.76Fe3+ 0.32Si7.84O22(OH)2. The long-range cation distribution in the two samples has been elucidated by in situ neutron powder diffraction revealing that Mn is preferentially ordered onto M(4) ? M(2) >M(1) >M(3) in both samples. Partitioning of Mn from M(4) into the octahedral sites begins at 350 °C, with site exchange energies of ?16.6 kJ mol?1 and ?14.9 kJ mol?1, in samples containing 1.90 and 1.57 Mn apfu, respectively. Mössbauer and infrared spectroscopy have been used to study the samples at room temperature, and Mössbauer data agree well with the diffraction results, confirming that high-temperature cation distributions are retained during cooling. The fine structure in the hydroxyl-stretching region of the IR absorption spectra has been used to discuss qualitatively the site occupancies of the coordinating M(1)M(3)M(1) triplet, linked by O(3). On the basis of such modelling, we conclude that a degree of local clustering is present in both samples.  相似文献   

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