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1.
We document the first occurrence of Fe‐rich olivine‐bearing migmatitic metapelite in the Khondalite Belt, North China Craton. Petrological analyses revealed two exotic assemblages of orthopyroxene+spinel+olivine and orthopyroxene+spinel+cordierite. Phase relation modelling suggests that these assemblages are diagnostic of ultra‐high temperature (UHT) metamorphism in the Fe‐rich system, with temperatures from 1,000 to 1,050°C at 0.6 GPa. U–Th–Pb SIMS analyses on zircon reveal a similar age of c. 1.92 Ga for the olivine‐bearing migmatite and an adjacent gabbronoritic intrusion that is therefore identified as the heat source for the UHT metamorphism. These results, coupled with additional analysis of the famous Tuguiwula sapphirine‐bearing granulite, lead to a re‐appraisal of the P–T path shape and heat source for the UHT metamorphism. We suggest that UHT metamorphism, dated between 1.92 and 1.88 Ga, across the whole Khondalite belt, proceeded from a clockwise P–T evolution with an initial near‐isobaric heating path at ~0.6–0.8 GPa, and a maximum temperature of 1,050°C followed by a cooling path with minor decompression to ~0.5 GPa. Considering our results and previous works, we propose that the orogenic crust underwent partial melting at temperature reaching 850°C and depth of ~20 to ~30 km during a period of c. 30 Ma, between 1.93 and 1.90 Ga. During this time span, the partially molten crust was continuously intruded by mafic magma pulses responsible for local greater heat supply and UHT metamorphism above 1,000°C. We propose that the UHT metamorphism in the Khondalite belt is not related to an extensional post‐collisional event, but is rather syn‐orogenic and associated with mafic magma supplies.  相似文献   

2.
Experiments with peridotite minerals in simple (MgO–Al2O3–SiO2,CaO–MgO–SiO2 and CaO–MgO–Al2O3–SiO2)and natural systems were conducted at 1300–1500°Cand 6–10 GPa using a multi-anvil apparatus. The experimentsin simple systems demonstrated consistency with previous lowerpressure experiments in belt and piston–cylinder set-ups.The analysis of spatial variations in pyroxene compositionswithin experimental samples was used to demonstrate that pressureand temperature variations within the samples were less than0·4 GPa and 50°C. Olivine capsules were used in natural-systemexperiments with two mineral mixtures: SC1 (olivine + high-Alorthopyroxene + high-Al clinopyroxene + spinel) and J4 (olivine+ low-Al orthopyroxene + low-Al clinopyroxene + garnet). Theexperiments produced olivine + orthopyroxene + garnet ±clinopyroxene assemblages, occasionally with magnesite and carbonate-richmelt. Equilibrium compositions were derived by the analysisof grain rims and evaluation of mineral zoning. They were comparedwith our previous experiments with the same starting mixturesat 2·8–6·0 GPa and the results from simplesystems. The compositions of minerals from experiments withnatural mixtures show smooth pressure and temperature dependencesup to a pressure of 8 GPa. The experiments at 9 and 10 GPa producedandradite-rich garnets and pyroxene compositions deviating fromthe trends defined by the lower pressure experiments (e.g. higherAl in orthopyroxene and Ca in clinopyroxene). This discrepancyis attributed to a higher degree of oxidation in the high-pressureexperiments and an orthopyroxene–high-P clinopyroxenephase transition at 9 GPa. Based on new and previous resultsin simple and natural systems, a new version of the Al-in-orthopyroxenebarometer is presented. The new barometer adequately reproducesexperimental pressures up to 8 GPa. KEY WORDS: garnet; mineral equilibrium; multi-anvil apparatus; orthopyroxene; geobarometry  相似文献   

3.
Olivine single crystals have been deformed under high confining pressure (P=5?GPa) and temperature (T=1400?°C) conditions in a multi-anvil high pressure apparatus. NaCl, diamond and NaCl+diamond (2:1 by volume) powders were encapsulated along with the olivine single crystals in order to produce a range of stress states. The change of the non-hydrostatic stress transmitted to the olivine samples, enclosed within these three different media, during heating has been evaluated by observation of dislocation microstructure and density. A higher differential stress can be generated with diamond powder (0.1?GPa) than with NaCl powder (0.02?GPa). Although an intermediate differential stress between 0.1?GPa and 0.02?GPa had been expected to be generated using NaCl+diamond powder, the generation of non-hydrostatic stress in the olivine sample was unsuccessful. This may be caused by the fact that compaction (or sintering) proceeded in the capsule throughout the experiments. The most important finding of these experiments is that a constant non-hydrostatic stress can be applied to a sample under very high pressure and temperature conditions within the multi-anvil high pressure apparatus for the duration of the experiment. This approach is therefore suitable for investigating the steady-state rheological properties of mantle minerals at near-mantle conditions.  相似文献   

4.
Summary Supra-solidus phase relations at temperatures and pressures ranging from 800 to 1700 °C and 2 to 6.4 GPa have been determined experimentally for three silica-rich lamproites: hyalo-leucite phlogopite lamproite (Oscar, West Kimberley); sanidine richterite lamproite (Cancarix, Murcia-Almeria); and phlogopite transitional madupitic lamproite (Middle Table Mountain, Wyoming). All samples have extended melting intervals (500–600 °C). Bulk composition has a significant control on the nature of the initial liquidus phases, with orthopyroxene occurring at low pressures (<4 GPa) in the relatively calcium-poor Oscar and Cancarix lamproites. At higher pressure (>6 GPa) orthopyroxene is replaced by garnet plus clinopyroxene as near-liquidus phases in the Oscar lamproite and by orthopyroxene plus clinopyroxene in the Cancarix sample. Clinopyroxene is a near-liquidus phase at all pressures in the Middle Table Mountain lamproite. Near-solidus phase assemblages at high pressure (>5 GPa) are: clinopyroxene + phlogopite + coesite + rutile + garnet (Oscar); clinopyroxene + garnet + coesite + K–Ti-silicate (Cancarix); clinopyroxene + phlogopite + apatite + K–Ti-silicate (Middle Table Mountain). In all compositions olivine is never found as a liquidus phase at any of the temperatures or pressures studied here. The phase relationships are interpreted to suggest that silica-rich lamproites cannot be derived by the partial melting of lherzolitic sources. Their genesis is considered to involve high degrees of partial melting of ancient metasomatic veins within a harzburgitic-lherzolitic lithospheric substrate mantle. The veins are considered in their mineralogy to be similar to the experimentally-observed, high pressure, near-solidus phase assemblages. The composition of silica-rich primary lamproite magmas differs between cratons as a consequence of differing mineralogical modes of the source veins and different relative contributions from the veins and wall-rocks to the partial melts. Received February 21, 2000; revised version accepted July 3, 2001  相似文献   

5.
The alpine-type ultrabasic rocks of the studied area have undergone plastic deformation under a temperature about 800--1200℃, a pressure about 0.9--1.68 GPa and differential stress of 0.2--0.35 GPa in relatively dry conditions, forming ultrabasie mylonite with porphyroclastic and mylonitic textures, Primary crystallized silicate melt inclusions and melt-fluid inclusions are discovered in porphyroclastic minerals and ore-forming chrome spinel. These rocks are formed under relatively stable physico-chemical conditions through liquid immiscibility of silicate melts, at 1200°-- 1300° and 1.1--1.38 GPa, equivalent to a depth of 40--50 km. No inclusion has been found in recrystallized secondary olivine and pyroxene, indicating that the plastic deformation happened after the formation of the rocks.  相似文献   

6.
Summary Mantle-derived xenoliths from Baarley in the Quaternary West Eifel volcanic field contain six distinct varieties of glass in veins, selvages and pools. 1) Silica-undersaturated glass rich in zoned clinopyroxene microlites that forms jackets around and veins within the xenoliths. This glass is compositionally similar to groundmass glass in the host basanite. 2) Silica-undersaturated alkaline glass that contains microlites of Cr-diopside, olivine and spinel associated with amphibole in peridotites. This glass locally contains corroded primary spinel and phlogopite. 3) Silica-undersaturated glass associated with diopside, spinel ± olivine and rh?nite microlites in partly to completely broken down amphibole grains in clinopyroxenites. 4) Silica-undersaturated to silica-saturated, potassic glass in microlite-rich fringes around phlogopite grains in peridotite. 5) Silica-undersaturated potassic glass in glimmerite xenoliths. 6) Silica-rich glass around partly dissolved orthopyroxene crystals in peridotites. Geothermometry of orthopyroxene–clinopyroxene pairs (P = 1.5 GPa) gives temperatures of ∼ 850 °C for unveined xenoliths to 950–1020 °C for veined xenoliths. Clinopyroxene – melt thermobarometry shows that Cr-diopside – type 2 glass pairs in harzburgite formed at 1.4 to 1.1 GPa and ∼ 1250 °C whereas Cr-diopside – type 2 glass pairs in wehrlite formed at 0.9 to 0.7 GPa and 1120–1200 °C. This bimodal distribution in pressure and temperature suggests that harzburgite xenoliths may have been entrained at greater depth than wehrlite xenoliths. Glass in the Baarley xenoliths has three different origins: infiltration of an early host melt different in composition from the erupted host basanite; partial melting of amphibole; reaction of either of these melts with xenolith minerals. The composition of type 1 glass suggests that jackets are accumulations of relatively evolved host magma. Mass balance modelling of the type 2 glass and its microlites indicates that it results from breakdown of disseminated amphibole and reaction of the melt with the surrounding xenolith minerals. Type 3 glass in clinopyroxenite xenoliths is the result of breakdown of amphibole at low pressure. Type 4 and 5 glass formed by reaction between phlogopite and type 2 melt or jacket melt. Type 6 glass associated with orthopyroxene is due to the incongruent dissolution of orthopyroxene by any of the above mentioned melts. Compositional gradients in xenolith olivine adjacent to type 2 glass pools and jacket glass can be modelled as Fe–Mg interdiffusion profiles that indicate melt – olivine contact times between 0.5 and 58 days. Together with the clinopyroxene – melt thermobarometry calculations these data suggest that the glass (melt) formed over a short time due to decompression melting of amphibole and infiltration of evolved host melt. None of the glass in these xenoliths can be directly related to metasomatism or any other process that occurred insitu in the mantle. Received November 23, 1999; revised version accepted September 5, 2001  相似文献   

7.
Single crystalline San Carlos olivine (1 mm cube) was transformed to (Mg,Fe)2SiO4β-phase at 13.5–15 GPa, 1030–1330 °C for 0–600 min using a multi-anvil high pressure apparatus. The α-β transformation occurred by incoherent surface nucleation and interface-controlled growth and recovered partially transformed samples showed sharply defined reaction rim. The growth rate of the β-phase rim significantly decreased with time and the growth eventually ceased. TEM observations revealed that many dislocations were created in both the relict olivine just near the α-β interface and the β-phase in the rim, which show evidence for deformation caused by interfacial stresses associated with the misfit elastic strain of the transformation. The observed tangled dislocation texture in β-phase suggested that the β-phase rim was hardened and relaxation of the interfacial stress was retarded. This probably caused a localized pressure drop in the relict olivine and decreased the growth rate. Time-dependent growth rates of β-phase is possibly controlled by the rheology of β-phase, which must be considered for the prediction of the olivine metastability in the subducting slabs. Received: 24 January 1997 / Revised, accepted: 24 July 1998  相似文献   

8.
Partial melting experiments on a San Carlos peridotite were done in a Walker type multi-anvil press at pressures from 5 to 12.5 GPa. Experiments were done in the presence of a COH-fluid and at oxygen fugacity controlled by the Fe–FeO buffer. Olivine, clinopyroxene, garnet and orthopyroxene are stable in all but the highest temperature 10 GPa experiments where olivine and garnet coexist, and the highest temperature 5 GPa experiments where olivine is the single crystalline phase. The solidus at 5 GPa was found to be at approximately 1,200°C and the liquidus was estimated to be at 1,325°C, which is ∼500°C lower than has been reported for dry melting of peridotite. The aluminum concentration of the melts decreases with increasing melt fraction and decreases also with increasing pressure. At 5 GPa the melts have a CaO/Al2O3-ratio of 0.85–1.0, which is similar to that of undepleted komatiites; major element concentrations are also identical to those of undepleted komatiites such as the Munro komatiites. At 10 and 12.5 GPa the partial melts have CaO/Al2O3-ratios above 1.5 and major element composition almost identical to aluminum depleted komatiites such as the Barberton komatiites. We therefore conclude that in the presence of a reducing COH-fluid both aluminum-depleted and -undepleted komatiites could have formed at temperatures much lower than generally accepted.  相似文献   

9.
Northern Victoria Land is a key area for the Ross Orogen – a Palaeozoic foldbelt formed at the palaeo‐Pacific margin of Gondwana. A narrow and discontinuous high‐ to ultrahigh‐pressure (UHP) belt, consisting of mafic and ultramafic rocks (including garnet‐bearing types) within a metasedimentary sequence of gneisses and quartzites, is exposed at the Lanterman Range (northern Victoria Land). Garnet‐bearing ultramafic rocks evolved through at least six metamorphic stages. Stage 1 is defined by medium‐grained garnet + olivine + low‐Al orthopyroxene + clinopyroxene, whereas finer‐grained garnet + olivine + orthopyroxene + clinopyroxene + amphibole constitutes the stage 2 assemblage. Stage 3 is defined by kelyphites of orthopyroxene + clinopyroxene + spinel ± amphibole around garnet. Porphyroblasts of amphibole replacing garnet and clinopyroxene characterize stage 4. Retrograde stages 5 and 6 consist of tremolite + Mg‐chlorite ± serpentine ± talc. A high‐temperature (～950 °C), spinel‐bearing protolith (stage 0), is identified on the basis of orthopyroxene + clinopyroxene + olivine + spinel + amphibole inclusions within stage 1 garnet. The P–T estimates for stage 1 are indicative of UHP conditions (3.2–3.3 GPa and 764–820 °C), whereas stage 2 is constrained between 726–788 °C and 2.6–2.9 GPa. Stage 3 records a decompression up to 1.1–1.3 GPa at 705–776 °C. Stages 4, 5 and 6 reflect uplift and cooling, the final estimates yielding values below 0.5 GPa at 300–400 °C. The retrograde P–T path is nearly isothermal from UHP conditions up to deep crustal levels, and becomes a cooling–unloading path from intermediate to shallow levels. The garnet‐bearing ultramafic rocks originated in the mantle wedge and were probably incorporated into the subduction zone with felsic and mafic rocks with which they shared the subsequent metamorphic and geodynamic evolution. The density and rheology of the subducted rocks are compatible with detachment of slices along the subduction channel and gravity‐driven exhumation.  相似文献   

10.
The mineralogy and petrology of pumice exposed in two small outcrops at the top of two hills in western Spain suggest that these rocks are of impact genesis. Ringwoodite, which was identified in the rocks, can crystallize from melt under pressures of 10?C11 GPa in static regime or at the relief of pressure of a shock wave under pressures of 15?C17 GPa and more. The other minerals crystallizing from the melt at a pressure decrease are ferrous hortonolite (unit cell parameters of ringwoodite and hortonolite are reported), minerals belonging to the spinel group and having variable Fe mole fractions, clinopyroxene, orthopyroxene, anorthite, and corundum. Hollow, skeleton, dendritic, and whisker crystals of these minerals suggest that they crystallized at the cooling and strong undercooling of the melt. The crystallization temperature of the hercynite is 1780°C. The temperature of the melt that produced the pumice is estimated at 1900?C2700°C. Our find of ringwoodite is the first discovery of this mineral in natural impact rocks.  相似文献   

11.
《Gondwana Research》2008,13(4):438-453
This paper presents a regional scale observation of metamorphic geology and mineral assemblage variations of Kontum Massif, central Vietnam, supplemented by pressure–temperature estimates and reconnaissance geochronological results. The mineral assemblage variations and thermobarometric results classify the massif into a low- to medium-temperature and relatively high-pressure northern part characterised by kyanite-bearing rocks (570–700 °C at 0.79–0.86 GPa) and a more complex southern part. The southern part can be subdivided into western and eastern regions. The western region shows very high-temperature (> 900 °C) and -pressure conditions characterised by the presence of garnet and orthopyroxene in both mafic and pelitic granulites (900–980 °C at 1.0–1.5 GPa). The eastern region contains widespread medium- to high-temperature and low-pressure rocks, with metamorphic grade increasing from north to south; epidote- or muscovite-bearing gneisses in the north (< 700–740 °C at < 0.50 GPa) to garnet-free mafic and orthopyroxene-free pelitic granulites in the south (790–920 °C at 0.63–0.84 GPa). The Permo-Triassic Sm–Nd ages (247–240 Ma) from high-temperature and -pressure granulites and recent geochronological studies suggest that the south-eastern part of Kontum Massif is composed of a Siluro-Ordovician continental fragment probably showing a low-pressure/temperature continental geothermal gradient derived from the Gondwana era with subsequent Permo-Triassic collision-related high-pressure reactivation zones.  相似文献   

12.
Recent petrological studies on high‐pressure (HP)–ultrahigh‐pressure (UHP) metamorphic rocks in the Moldanubian Zone, mainly utilizing compositional zoning and solid phase inclusions in garnet from a variety of lithologies, have established a prograde history involving subduction and subsequent granulite facies metamorphism during the Variscan Orogeny. Two temporally separate metamorphic events are developed rather than a single P–T loop for the HP–UHP metamorphism and amphibolite–granulite facies overprint in the Moldanubian Zone. Here further evidence is presented that the granulite facies metamorphism occurred after the HP–UHP rocks had been exhumed to different levels of the middle or upper crust. A medium‐temperature eclogite that is part of a series of tectonic blocks and lenses within migmatites contains a well‐preserved eclogite facies assemblage with omphacite and prograde zoned garnet. Omphacite is partly replaced by a symplectite of diopside + plagioclase + amphibole. Garnet and omphacite equilibria and pseudosection calculations indicate that the HP metamorphism occurred at relatively low temperature conditions of ~600 °C at 2.0–2.2 GPa. The striking feature of the rocks is the presence of garnet porphyroblasts with veins filled by a granulite facies assemblage of olivine, spinel and Ca‐rich plagioclase. These minerals occur as a symplectite forming symmetric zones, a central zone rich in olivine that is separated from the host garnet by two marginal zones consisting of plagioclase with small amounts of spinel. Mineral textures in the veins show that they were first filled mostly by calcic amphibole, which was later transformed into granulite facies assemblages. The olivine‐spinel equilibria and pseudosection calculations indicate temperatures of ~850–900 °C at pressure below 0.7 GPa. The preservation of eclogite facies assemblages implies that the granulite facies overprint was a short‐lived process. The new results point to a geodynamic model where HP–UHP rocks are exhumed to amphibolite facies conditions with subsequent granulite facies heating by mantle‐derived magma in the middle and upper crust.  相似文献   

13.
Experimental modelling of corona textures   总被引：1，自引：0，他引：1  
Formation of corona textures along olivine–plagioclase and orthopyroxene–plagioclase interfaces has been experimentally reproduced at 670 and 700 °C and 5 kbar with either a pure H2O fluid phase or 0.1 and 37 m NaCl–H2O solution fluid. In these experiments, we investigate the interaction of primary olivine and/or orthopyroxene and plagioclase in powders and polished crystals, and in small samples of a natural gabbro. The experiments result in the formation of corona textures with several layers of different assemblages (according to the experimental conditions) consisting of garnet (grossular), clinopyroxene, orthopyroxene, amphibole, chlorite and phlogopite. The experiments show major differences in the number of layers, the mineral assemblages and mineral composition, and in the trends of composition of plagioclase in coronas around olivine and orthopyroxene. The fluid phase composition influences the corona assemblages and the composition of the minerals in the experimental coronas; for example, garnet appears in the coronas in the second experiment where the NaCl–H2O ratio is low. Experimental modelling of corona textures confirms a model of simultaneous growth of layers by the mechanism of diffusion metasomatism with participation of a fluid phase through which mass is transferred. Zoning in the experimental coronas shows opposing diffusion of Al and Ca from plagioclase and Mg and Fe from olivine/orthopyroxene; difference in the mobility of the components is inferred from observations in the coronas. The experimental corona textures are compared with natural coronas from the Belomorian belt (Baltic shield), developed at 670–690 °C and 7–8 kbar, and the Marun‐Keu complex (Polar Urals), developed at 670–700 °C and 14–16 kbar, where the corona textures correspond to a transitional stage of the gabbro‐to‐eclogite transformation.  相似文献   

14.
Numerous lenticular bodies of ultramafic rocks occur withinthe upper amphibolite- to granulitefacies metamorphic terraneof the Austrides between the Non and Ultimo valleys (Nonsbergregion), northern Italy. The ultramafic rocks are divided intotwo textural types: (a) coarse-type; and (b) finetype. The coarse-typerocks have the protogranular texture and are predominantly spinellherzolite. Some coarse-type spinel lherzolites have partlytransformed to garnet lherzolite. The fine-types are consideredto be metamorphic derivatives of the former, and the observedmineral assemblages are: (1) olivine + orthopyroxene + clinopyroxene+ garnet + amphibole ? spinel, (2) olivine + orthopyroxene +garnet + amphibole + spinel; (3) olivine + orthopyroxene + amphibole+ spinel; and (4) olivine+ orthopyroxene + amphibole + chlorite.Based on the microprobe analyses of constituent minerals fromten representative peridotite samples, physical conditions ofthe metamorphism, particularly that of the spinel to garnetlherzolite transformation, are estimated. Applications of pyroxenegeothermometry yield temperature estimates of 1100–1300?Cfor the formation of the primary spinel lherzolite, and 700–800?Cfor that of the fine-type peridotites. A pressure range of 16–28kb is obtained for the garnet lherzolite crystallization dependingon the choice of geobarometers. Two alternative P-T paths, i.e.(1) isobaric cooling or (2) pressure-increase and temperaturedecrease are considered and their geodynamic implications discussed.  相似文献   

15.
Studies of mass transport and kinetics in minerals at high pressure often require a sample environment in which the stress is near-hydrostatic and the chemical environment is carefully controlled. We report here details of a multianvil sample assembly in which these requirements are fulfilled and which has been used to study the effect of pressure on the kinetics of dislocation recovery in olivine up to 10 GPa. Annealing experiments have been performed on single crystals of San Carlos olivine at 8.5 GPa and 1400° C in a 1200 tonne split-sphere multianvil apparatus. The sample assembly consists of an 18 mm MgO octahedron with a LaCrO3 heater of variable wall thickness to give a small temperature variation (20° C) along the 3 mm length of the sample capsule. To minimize the differential stress on the sample, the olivine single crystal is surrounded by NaCl and both pressurization and depressurization are performed slowly at a temperature of 600° C (to minimize the strength of the NaCl). The silica activity is buffered by orthopyroxene powder in contact with the olivine and the oxygen fugacity is buffered by Ni + NiO within the sample capsule. The H2O-content of the sample assembly is minimized by drying all components at 230° C under vacuum. Olivine single crystals recovered after annealing at 1400° C and 8.5 GPa show no evidence of deformation, either ductile or brittle. Dislocation densities of 109–1010 m-2 are similar to those observed prior to high-pressure annealing and indicate differential stresses of <10 mpa.=" infrared=" spectroscopy=" indicates=" that=" the=" hydrogen=" content=" of=" a=" sample=" annealed=" at=" 10=" gpa,=" 1500°=" c=" for=" 21=" h=" is=">13 H/106Si, which, although low, is higher than that of the crystals prior to high-pressure annealing. Finally, the effectiveness of the fO2 buffer has been verified by estimating the fO2 at the surface of the sample from the solubility of Fe in Pt metal in equilibrium with the olivine and orthopyroxene.  相似文献   

16.
Polycrystalline ruby (α-Al2O3:Cr3+), a widely used pressure calibrant in high-pressure experiments, was compressed to 68.1 GPa at room temperature under non-hydrostatic conditions in a diamond anvil cell. Angle-dispersive X-ray diffraction experiments in a radial geometry were conducted at beamline X17C of the National Synchrotron Light Source. The stress state of ruby at high pressure and room temperature was analyzed based on the measured lattice strain. The differential stress of ruby increases with pressure from ~3.4 % of the shear modulus at 18.5 GPa to ~6.5 % at 68.1 GPa. The polycrystalline ruby sample can support a maximum differential stress of ~16 GPa at 68.1 GPa under non-hydrostatic compression. The results of this study provide a better understanding of the mechanical properties of this important material for high-pressure science. From a synthesis of existing data for strong ceramic materials, we find that the high-pressure yield strength correlates well with the ambient pressure Vickers hardness.  相似文献   

17.
Pressure–temperature conditions of tourmaline breakdown in a metapelite were determined by high-pressure experiments at 700–900°C and 4–6 GPa. These experiments produced an eclogite–facies assemblage of garnet, clinopyroxene, phengite, coesite, kyanite and rare rutile. The modal proportions of tourmaline clearly decreased between 4.5 and 5 GPa at 700°C, between 4 and 4.5 GPa at 800°C, and between 800 and 850°C at 4 GPa, with tourmaline that survived the higher temperature conditions appearing corroded and thus metastable. Decreases in the modal abundance of tourmaline are accompanied by decreasing modal abundance of coesite, and increasing that of clinopyroxene, garnet and kyanite; the boron content of phengite increases significantly. These changes suggest that, with increasing pressure and temperature, tourmaline reacts with coesite to produce clinopyroxene, garnet, kyanite, and boron-bearing phengite and fluid. Our results suggest that: (1) tourmaline breakdown occurs at lower pressures and temperatures in SiO2-saturated systems than in SiO2-undersaturated systems. (2) In even cold subduction zones, subducting sediments should release boron-rich fluids by tourmaline breakdown before reaching depths of 150 km, and (3) even after tourmaline breakdown, a significant amount of boron partitioned into phengite could be stored in deeply subducted sediments.  相似文献   

18.
We performed an experimental study, designed to reproduce the formation of an unusual merwinite?+?olivine-bearing mantle assemblage recently described as a part of a Ca-rich suite of inclusions in sublithospheric diamonds, through the interaction of peridotite with an alkali-rich Ca-carbonatite melt, derived from deeply subducted oceanic crust. In the first set of experiments, we studied the reaction between powdered Mg-silicates, olivine and orthopyroxene, and a model Ca-carbonate melt (molar Na:K:Ca?=?1:1:2), in a homogeneous mixture, at 3.1 and 6.5 GPa. In these equilibration experiments, we observed the formation of a merwinite?+?olivine-bearing assemblage at 3.1 GPa and 1200 °C and at 6.5 GPa and 1300–1400 °C. The melts coexisting with this assemblage have a low Si and high Ca content (Ca#?=?molar 100?×?Ca/(Ca?+?Mg)?>?0.57). In the second set of experiments, we investigated reaction rims produced by interaction of the same Ca-carbonate melt (molar Na:K:Ca?=?1:1:2) with Mg-silicate, olivine and orthopyroxene, single crystals at 3.1 GPa and 1300 °C and at 6.5 GPa and 1400 °C. The interaction of the Ca-carbonate melt with olivine leads to merwinite formation through the expected reaction: 2Mg2SiO4 (olivine)?+?6CaCO3 (liquid)?=?Ca3MgSi2O8 (merwinite)?+?3CaMg(CO3)2 (liquid). Thus, our experiments confirm the idea that merwinite in the upper mantle may originate via interaction of peridotite with Ca-rich carbonatite melt, and that diamonds hosting merwinite may have a metasomatic origin. It is remarkable that the interaction of the Ca-carbonate melt with orthopyroxene crystals does not produce merwinite both at 3.1 and 6.5 GPa. This indicates that olivine grain boundaries are preferable for merwinite formation in the upper mantle.  相似文献   

19.
 Using the high-pressure differential thermal analysis (HP-DTA) system in a cubic multianvil high-pressure apparatus, we measured the melting points of portlandite, Ca(OH)2, up to 6 GPa and 1000 °C. We detected endothermic behavior at the temperature and pressure conditions of 800 °C and 2.5 GPa, 769 °C and 3.5 GPa, 752 °C and 4.0 GPa, 686 °C and 5.0 GPa, and 596 °C and 6.0 GPa, respectively, due to melting of portlandite. By in situ X-ray studies under pressure, the melting of portlandite was observed at 730 °C and 4.32 GPa and at 640 °C and 5.81 GPa, respectively. Results of both HP-DTA and X-ray studies were consistent within experimental error. The melting is congruent and has a negative Clapeyron slope, indicating that liquid Ca(OH)2 has higher densities than crystalline portlandite in this pressure range. Received: 19 June 1999 / Revised, accepted: 11 September 1999  相似文献   

20.
The Dergaon fall represents a shock-melted H4-5(S5) ordinary chondrite which includes at least ten textural varieties of chondrules and belongs to the high chondrule-matrix ratio type.Our study reveals that the chondrules are of diverse mineralogy with variable olivine-pyroxene ratios(Type Ⅱ),igneous melt textures developed under variable cooling rates and formed through melt fractionations from two different melt reservoirs.Based on the experimental analogues,mineralogical associations and phase compositions,it is suggested that the Dergaon chondrules reflect two contrasting environments:a hot,dust-enriched and highly oxidized nebular environment through melting,without significant evaporation,and an arrested reducing environment concomitant with major evaporation loss of alkali and highly volatile trace elements.Coexistence of chlorapatite and merrillite suggests formation of the Dergaon matrix in an acidic accretionary environment.Textural integration and chemical homogenization occurred at ~ 1 atmospheric pressure and a mean temperature of 765 C mark the radiogenic thermal event.Equilibrated shock features(olivine mosaicism,diaplectic plagioclase,polycrystalline troilite) due to an impact-induced thermal event reflect a shock pressure 45 GPa and temperature of 600 C.By contrast,the local disequilibrium shock features(silicate melt veins comprising of olivine crystallites,troilite melt veins and metal droplets) correspond to a shock pressure up to 75 GPa and temperature950 ℃.  相似文献   

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