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1.
An olivine basalt, a tonalite (andesite), a granite (rhyolite), and a red clay (pelagic sediment) were reacted, with known quantities of water in sealed noble metal capsules, in a piston-cylinder apparatus at 30 kb pressure. For the pelagic sediment, with H2O+=7.8% and no additional water, the liquidus temperature is 1240°C, the primary phases are garnet and kyanite. The subsolidus phase assemblage is phengite mica+garnet+clinopyroxene+coesite+kyanite. With 5 wt.% water added, the liquidus temperatures and primary phases for the calc-alkaline rocks are 1280°-1180°-1080°, garnet+clinopyroxene, garnet, and quartz respectively. Garnet and clinopyroxene occur throughout the melting interval of the olivine tholeiite for all water contents. Garnet is joined by clinopyroxene 80° below the andesite plus 5% H2O liquidus, quartz is joined by clinopyroxene 180° below the rhyolite plus 5% H2O liquidus. The subsolidus phase assemblage is garnet+clinopyroxene+coesite+minor kyanite for all the calc-alkaline compositions. We conclude that calc-alkaline andesites and rhyolites are not equilibrium partial melting pruducts of subducted oceanic crust consisting of olivine tholeiite basalt and siliceous sediments. Partial melting in subduction zones produces broadly acid and intermediate liquids, but these liquids lie off the calc-alkaline basalt-andesite-rhyolite join and must undergo modification at lower pressures to produce calcalkaline magmas erupted in overlying island arcs.  相似文献   

2.
The oxygen isotope compositions of coesite, sanidine, kyanite, clinopyroxene and garnet were measured in an ultra-high pressure-temperature grospydite from the Roberts Victor kimberlite, South Africa. The 18O values (per mil v. SMOW) of each phase and (1 ) are as follows: coesite, 8.62 (0.31); sanidine, 8.31 (0.02); kyanite, 7.98 (0.08); pyroxene, 7.63 (0.11); garnet, 7.53 (0.03). In situ analyses of the coesite with the laser extraction system are 18O=9.35 (0.08), n=4, demonstrating that the coesite is homogeneous. The coesite has partially inverted to polycrystalline quartz and the pyroxene is extensively altered during uplift. The larger scatter for the mineral separate coesite and pyroxene data may be due to partial reequilibration between the decompression-related breakdown products of these two phases. The anomalously high 18O value of the grospydite (18Owholerock=7.7) is consistent with altered oceanic crust as a source rock. Temperature estimates from a linear regression of all the data to three different published calibrations correspond to an equilibrium temperature of 1310±80°C. The calculated isotopic pressure effect is to lower these estimates by about 40°C at 40 kb. The estimated temperature based on Al–Si disorder in sanidine is 1200±100°C and that from Fe–Mg exchange thermometry between garnet and clinopyroxene is 1100±50°C. Given the large errors associated with thermometry at such high temperatures, it is concluded that the xenolith equilibrated that 1200±100°C. Pressure estimates are 45±5 kb, based on dilution of the univariant equilibria albite = jadeite + coesite and 2 kyanite + 3 diopside = grossular + pyrope + 2coesite. Zoning in the outer 20 m of the feldspar from Ab0.8 to Ab16 indicates rapid decompression to 25 kb or less. The isotopic temperature estimates are the highest ever obtained and combined with the high degree of Al–Si disorder in sanidine require rapid cooling from ultra-high temperatures. It is inferred that the xenolith was sampled at the time of equilibration, providing a point on the upper Cretaceous geotherm in the mantle below South Africa.  相似文献   

3.
Petrochemistry of eclogites from the Koidu Kimberlite Complex,Sierra Leone   总被引：1，自引：0，他引：1  
Petrography, mineral and bulk chemistry of upper mantle-derived eclogites (garnet and clinopyroxene) from the Koidu Kimberlite Complex, Sierra Leone, are presented in the first comprehensive study of these xenoliths from West Africa. Although peridotite-suite xenoliths are generally more common in kimberlites, the upper mantle sample preserved in Pipe Number 1 at Koidu is exclusively eclogitic, making this the fifth locality in which eclogite is the sole polymineralic xenolith in kimberlite. Over 2000 xenoliths were collected, of which 47 are described in detail that include diamond, graphite, kyanite, corundum, quartz after coesite, and amphibole eclogites. Grossular-pyrope-almandine garnets are chromium-poor (<0.72 wt% Cr2O3) and fall into two distinct groups based on magnesium content. High-MgO garnets have an average composition of Pyr67Alm22Gross11, low-MgO garnets are grossular- and almandine-rich with an average composition of Gross34Pyr33Alm33. Clinopyroxenes are omphacitic with a range in jadeite contents from 7.7 to 70.1 mol%. Three eclogites contain zoned and mantled garnets with almandine-rich cores and pyrope-rich rims, and zoned clinopyroxenes with diopside-rich cores and jadeite-rich rims, and are among a very rare group of eclogites reported on a world-wide basis. The bulk compositions of eclogites have ranges comparable to that of basalts. High-MgO eclogites (16–20 wt% MgO) have close chemical affinities to picrites, whereas low-MgO eclogites (6–13 wt% MgO) are similar to alkali basalts. High-MgO eclogites contain high-MgO garnets and jadeiterich clinopyroxenes. Low-MgO eclogites contain low-MgO garnets, diopside and omphacite, and the group of primary accessory phases (diamond, graphite, quartz after coesite, kyanite, and corundum); grospydites are peraluminous. Estimated temperatures and pressures of equilibration of diamond-bearing eclogites, using the diamond-graphite stability curve and the Ellis and Green (1979) geothermometer, are 1031°–1363° C at 45–50 kb.K D values of Fe-Mg in garnet and clinopyroxene range from 2.3 to 12.2. Diamonds in eclogites are green, yellow, and clear, and range from cube to octahedral morphologies; the entire spectrum in color and morphology is present in a single metasomatized eclogite with zoned garnet and clinopyroxene. Ages estimated from Sm-Nd mineral isochrons range from 92–247 Ma. Nd values range from +4.05 to 5.23. Values of specific gravity range from 3.06–3.60 g/cc, with calculated seismic Vp of 7.4–8.7 km/s. Petrographie, mineral, and bulk chemical data demonstrate an overall close similarity between the Koidu xenolith suite and upper mantle eclogites from other districts in Africa, Siberia and the United States. At least two origins are implied byP-T, bulk chemistry and mineral compositions: low-MgO eclogites, with diamond and other accessory minerals, are considered to have formed from melts trapped and metamorphically equilibrated in the lithosphere; high-MgO eclogites are picritic and are the products of large degrees of partial melting, with equilibration in the asthenosphere. Fluid or diluted melt metasomatism is pervasive and contributed here and elsewhere to the LIL and refractory silicate incompatible element signature in kimberlites and lamproites, and to secondary diamond growth.  相似文献   

4.
Clinopyroxene and orthopyroxene megacrysts with lamellar intergrowths of pyroxenes and garnet rarely survive in pyroxenite layers from the exposed spinel-lherzolite massifs because of the emplacement history into the crust. Such features are remarkably preserved in some thick bands (up to 1 m) from the Freychinède ultramafic body (Ariège, French Pyrenees). These bands display a symmetrical zoning from the edges to the centre due to the concurrent decrease of orthopyroxene/clinopyroxene and spinel/garnet modal ratios. Textural and chemical data suggest that the present pyroxenite parageneses resulted from subsolidus recrystallization of magmatic assemblages composed of Al-rich orthopyroxene and clinopyroxene with minor spinel. These primary assemblages were changed by subsolidus recrystallization connected with an isobaric cooling at upper-mantle depth (45–50 km) from solidus temperature (1250°C) down to steady equilibrium temperature (950° C). The primary Al-rich ortho-and clinopyroxenes behaved differently on cooling. In a first stage, orthopyroxene exsolved concomitant Al-rich clinopyroxene and garnet, whereas clinopyroxene exsolved only Al-rich orthopyroxene. The garnet exsolution in clinopyroxene host is delayed to lower temperatures. This multistage process could account for the contrasting shapes of diffusion gradients adjacent to exsolved garnet, which tend to be flat in host-orthopyroxene and steep in host-clinopyroxene. An independent thermal modelling, together with available Al-diffusion data in clinopyroxene, allows us to define a fast magmatic cooling followed by a two-stage subsolidus cooling (35° C/year-6 from 1250° C to 1050° C and 9° C/year-6 to 900° C). This matches the contrasted exsolution sequences observed in the pyroxene megacrysts.  相似文献   

5.
In a bimineralic eclogite xenolith (sample JJG41) from the Roberts Victor kimberlite, compositional gradients in clinopyroxene are related to garnet exsolution. Two principal reactions involving clinopyroxene and garnet occur: (i) The net-transfer Al2Si-1Mg-1 which is responsible for garnet growth according to the equation 2Di+Al2Si-1Mg-1=Grossular+MgCa-1 (reaction 1). This has created substantial compositional gradients in Al, Si and Mg within clinopyroxene. (ii) The exchange of Fe–Mg between garnet and clinopyroxene (reaction 2). During the stage of garnet growth (reaction 1) the lamellae crystallized sequentially as a result of a temperature decrease from around 1400 to 1200° C. This exsolution growth-stage was under the control of Al diffusion in clinopyroxene and at around 1200° C further growth of garnet lamellae became impeded by the sluggishness of Al diffusion in the clinopyroxene host. However, reaction 2 continued during further cooling down to about 1000° C; this temperature being inferred from the constant Fe–Mg partitioning at clinopyroxene-garnet interfaces for the whole set of lamellae. The initial clinopyroxene in JJG41 was probably formed by crystallization from a melt in Archaean time. The cessation of Fe–Mg exchange between garnet and clinopyroxene at about 1000° C may well predate the eruption of the eclogite in kimberlite at around 100 Ma. Kinetic models of reaction are examined for both reactions. Modelling of reaction 1, involving both diffusion and interface migration, allows several means of estimating the diffusion coefficient of Al in clinopyroxene; the estimates are in the range 10-16-10-20 cm2/s at 1200° C. These estimates bracket the experimentally determined data for Al diffusion in clinopyroxene, and from these experimental data a preferred cooling rate of about 300° C/Ma is obtained for the period of growth of garnet exsolution lamellae. A geospeedometry approach (Lasaga 1983) suitable for a pure-exchange process (reaction 2) is used to estimate the cooling rate in the later stages of the thermal history (after garnet growth); values 4–40° C/Ma are consistent with the shape of the Fe-diffusion gradients in the clinopyroxene. The extensive thermal history recorded by JJG41, including probable melt involvement at ca. 1400° C, demonstrates the complex evolution of rocks within the mantle. Whilst the notion of formation of mantle eclogites from subducted oceanic crust has become fashionable, it is clear that tracing eclogite geochemical and P-T characteristics backwards from their nature at the time of xenolith eruption, through high-temperature mantle events to the characteristics of the original subducted oceanic crust, will be very complex.  相似文献   

6.
Petrographic, chemical and mineralogical data are presented on the Oetztal eclogites and their co-existing minerals. The available evidence indicates that they constitute the metamorphic derivates of an original gabbroic rock, the plagioclase and clinopyroxene of which reacted to form the garnet, omphacite and kyanite components of the eclogites. According to the available subsolidus experimental data these reactions are believed to have taken place in a 6–10 kb pressure range at about 550°–750° C.  相似文献   

7.
Six crystalline mixtures, picrite, olivine-rich tholeiite, nepheline basanite, alkali picrite, olivine-rich basanite, and olivine-rich alkali basalt were recrystallized at pressures to 40 kb, and the phase equilibria and sequences of phases in natural basaltic and peridotitic rocks were investigated.The picrite was recrystallized along the solidus to the assemblages (1) olivine+orthopyroxene+ clinopyroxene +plagioclase+spinel below 13 kb, (2) olivine+orthopyroxene+clinopyroxene+spinel between 13 kb and 18 kb, (3) olivine+orthopyroxene+clinopyroxene+ garnet+spinel between 18 kb and 26 kb, and (4) olivine+clinopyroxene+garnet above 26 kb. The solidus temperature at 1 atm is slightly below 1,100° and rises to 1,320° at 20 kb and 1,570° at 40 kb. Olivine is the primary phase crystallizing from the melt at all pressures to 40 kb.The olivine-rich tholeiite was recrystallized along the solidus into the assemblages (1) olivine+ clinopyroxene+plagioclase+spinel below 13 kb, (2) clinopyroxene+orthopyroxene+ spinel between 13 kb and 18 kb, (3) clinopyroxene+garnet+spinel above 18 kb. The solidus temperature is slightly below 1,100° at 1 atm, 1,370° at 20 kb, and 1,590° at 40 kb. The primary phase is olivine below 20 kb but is orthopyroxene at 40 kb.In the nepheline basanite, olivine is the primary phase below 14 kb, but clinopyroxene is the first phase to appear above 14 kb. In the alkali-picrite the primary phase is olivine to 40 kb. In the olivine-rich basanite, olivine is the primary phase below 35 kb and garnet is the primary phase above 35 kb. In the olivine-rich alkali basalt the primary phase is olivine below 20 kb and is garnet at 40 kb.Mineral assemblages in a granite-basalt-peridotite join are summarized according to reported experimental data on natural rocks. The solidus of mafic rock is approximately given by T=12.5 P Kb+1,050°. With increasing pressure along the solidus, olivine disappears by reaction with plagioclase at 9 kb in mafic rocks and plagioclase disappears by reaction with olivine at 13 kb in ultramafic rocks. Plagioclase disappears at around 22 kb in mafic rocks, but it persists to higher pressure in acidic rocks. Garnet appears at somewhat above 18 kb in acidic rocks, at 17 kb in mafic rocks, and at 22 kb in ultramafic rocks.The subsolidus equilibrium curves of the reactions are extrapolated according to equilibrium curves of related reactions in simple systems. The pyroxene-hornfels and sanidinite facies is the lowest pressure mineral facies. The pyroxene-granulite facies is an intermediate low pressure mineral facies in which olivine and plagioclase are incompatible and garnet is absent in mafic rocks. The low pressure boundary is at 7.5 kb at 750° C and at 9.5 kb at 1,150° C. The high pressure boundary is 8.0 kb at 750° C and 15.0 kb at 1,150° C. The garnet-granulite facies is an intermediate high pressure facies and is characterized by coexisting garnet and plagioclase in mafic rocks. The upper boundary is at 10.3 kb at 750° C and 18.0 kb at 1,150° C. The eclogite facies is the highest pressure mineral facies, in which jadeite-rich clinopyroxene is stable.Compositions of minerals in natural rocks of the granulite facies and the eclogite facies are considered. Clinopyroxenes in the granulite-facies rocks have smaller jadeite-Tschermak's molecule ratios and higher amounts of Tschermak's molecule than clinopyroxenes in the eclogite-facies rocks. The distribution coefficients of Mg between orthopyroxene and clinopyroxene are normally in the range of 0.5–0.6 in metamorphic rocks in the granulite facies. The distribution coefficients of Mg between garnet and clinopyroxene suggest increasing crystallization temperature of the rocks in the following order: eclogite in glaucophane schist, eclogite and granulite in gneissic terrain, garnet peridotite, and peridotite nodules in kimberlite.Temperatures near the bottom of the crust in orogenic zones characterized by kyanitesillimanite metamorpbism are estimated from the mineral assemblages of metamorphic rocks in Precambrian shields to be about 700° C at 7 kb and 800° C at 9 kb, although heat-flow data suggest that the bottom of Precambrian shield areas is about 400° C and the eclogite facies is stable.The composition of liquid which is in equilibrium with peridotite is estimated to be close to tholeiite basalt at the surface pressure and to be picrite at around 30 kb. The liquid composition becomes poorer in normative olivine with decreasing pressure and temperature.During crystallization at high pressure, olivine and orthopyroxene react with liquid to form clinopyroxene, and a discontinuous reaction series, olivine orthopyroxene clinopyroxene is suggested. By fractional crystallization of pyroxenes the liquid will become poorer in SiO2. Therefore, if liquid formed by partial melting of peridotite in the mantle slowly rises maintaining equilibrium with the surrounding peridotite, the liquid will become poorer in MgO by crystallization of olivine, and tholeiite basalt magma will arrive at the surface. On the other hand, if the liquid undergoes fractional crystallization in the mantle, the liquid may change in composition to alkali-basalt magma and alkali-basalt volcanism may be seen at a late stage of volcanic activity.Publication No. 681, Institute of Geophysics and Planetary Physics, University of California, Los Angeles.  相似文献   

8.
Beginning of melting and subsolidus relationships in the system K2O-CaO-Al2O3-SiO2-H2O have been experimentally investigated at pressures up to 20 kbars. The equilibria discussed involve the phases anorthite, sanidine, zoisite, muscovite, quartz, kyanite, gas, and melt and two invariant points: Point [Ky] with the phases An, Or, Zo, Ms, Qz, Vapor, and Melt; point [Or] with An, Zo, Ms, Ky, Qz, Vapor, and Melt.The invariant point [Ky] at 675° C and 8.7 kbars marks the lowest solidus temperature of the system investigated. At pressures above this point the hydrated phases zoisite and muscovite are liquidus phases and the solidus temperatures increase with increasing pressure. At 20 kbars beginning of melting occurs at 740 °C. The solidus temperatures of the quinary system K2O-CaO-Al2O3-SiO2-H2O are almost 60° C (at 20 kbars) and 170° C (at 2kbars) below those of the limiting quaternary system CaO-Al2O3-SiO2-H2O.The maximum water pressure at which anorthite is stable is lowered from 14 to 8.7 kbars in the presence of sanidine. The stability limits of anorthite+ vapor and anorthite+sanidine+vapor at temperatures below 700° C are almost parallel and do not intersect. In the wide temperature — pressure range at pressures above the reaction An+Or+Vapor = Zo+Ms+Qz and temperatures below the melting curve of Zo+Ms+Ky+Qz+Vapor, the feldspar assemblage anorthite+sanidine is replaced by the hydrated phases zoisite and muscovite plus quartz. CaO-Al2O3-SiO2-H2O. Knowledge of the melting relationships involving the minerals zoisite and muscovite contributes to our understanding of the melting processes occuring in the deeper parts of the crust. Beginning of melting in granites and granodiorites depends on the composition of plagioclase. The solidus temperatures of all granites and granodiorites containing plagioclases of intermediate composition are higher than those of the Ca-free alkali feldspar granite system and below those of the Na-free system discussed in this paper.The investigated system also provides information about the width of the P-T field in which zoisite can be stable together with an Al2SiO5 polymorph plus quartz and in which zoisite plus muscovite and quartz can be formed at the expense of anorthite and potassium feldspar. Addition of sodium will shift the boundaries of these fields to higher pressures (at given temperatures), because the pressure stability of albite is almost 10kbars above that of anorthite. Assemblages with zoisite+muscovite or zoisite+kyanite are often considered to be products of secondary or retrograde reactions. The P-T range in which hydration of granitic compositions may occur in nature is of special interest. The present paper documents the highest temperatures at which this hydration can occur in the earth's crust.  相似文献   

9.
The sub-solidus fields of crystallization of a spectrum of synthetic aluminous basic compositions (high-alumina basalt, anorthite-enriched high-alumina basalt, kyanite eclogite, grosspydite and gabbroic anorthosite) have been investigated at pressures of up to 36 kb. At low pressures the assemblages are characterized by abundant plagioclase, clinopyroxene and possibly minor olivine and orthopyroxene. These correspond to natural gabbroic and pyroxene granulite assemblages. As pressure is increased garnet appears and increases gradually in amount at the expense of other ferromagnesian minerals and plagioclase, until finally at pressures of >23 kb at 1,100° C, plagioclase disappears and high pressure clinopyroxene+garnet+kyanite±quartz assemblages equivalent to eclogite are obtained. In the eclogite stability field, with further rise in pressure, the ratio ga/cpx and the grossular content of the garnet increase.In the high-alumina basalt composition the transitional garnet granulite assemblage (clinopyroxene+plagioclase+garnet±quartz) is spread over a pressure interval of 11 kb at 1,100° C. This is a greater interval than observed for other basalt compositions and is important in considering the hypothesis that the Mohorovicic Discontinuity is a phase change from basalt to eclogite. It indicates that the change in V p would be spread over a significant depth range, and no sharp seismic velocity discontinuity could result.The first experimental synthesis of kyanite eclogite from both high-alumina basalt and kyanite eclogite compositions has been obtained, as well as synthesis of unusual grossular-clinopyroxene-kyanite assemblages (grosspydite) from grosspydite and gabbroic anorthosite compositions. The pressures needed to synthesize these assemblages are somewhat greater than the pressures needed to synthesize eclogite from basic compositions of lower alumina content at the same temperature. Experimental confirmation of the observation that there is a direct relation between Gross/Alm + Py ratio of garnet and the Jd/Di ratio of co-existing pyroxene in grosspydite and kyanite eclogite assemblages found in kimberlite pipes has also been obtained.  相似文献   

10.
A xenolith from the kimberlite pipe of the Roberts Victor Mine, O.F.S. shows a marginal rim rich in garnet (Py50Alm35Gro15), presumably resulting from reaction between the grospyditic inclusion and kimberlitic host. Similarity between the reaction rim-garnets, and those of the common mafic inclusion of the Roberts Victor pipe, suggests that the rare grospydite inclusions are accidental xenoliths, not directly related in origin to the kimberlites in which they are found.  相似文献   

11.
The results of complex study of silicate globules and α-quartz paramorphs after coesite in kyanite from grospydites from the Zagadochnaya kimberlite pipe, Yakutia, using optical and scanning electron spectroscopy, electron and ion microprobes, LA ICP MS and Raman spectroscopy, are presented. The existence of radial fractures diverging from silicate globules into the matrix (kyanite) attests to the fact that the content of the globules is extremely condensed. A zonal structure is usually typical for globules: a coat and a core, which can be explicitly distinguished under the electron microscope, can be differentiated in them. Compositionally, the coat of the globule corresponds to potassium feldspar (wt %: 66.4 SiO2; 16.9 Al2O3; 0.4 FeO; 0.1 CaO; 0.2 Na2O; 14.7 K2O). The globules were also detected in which along with K, a high content of Na and Ca was also ascertained in the silicate coat. The globule coat is considerably enriched with Ba, La, Ce, Nb, and a number of other noncompatible elements as compared with xenolith minerals. The water content in globules is ∼0.6 wt %. As compared with the host mineral (kyanite), the core part of the globules is also enriched with Co, Ni, Zn, and Cu; their content in kyanite is negligibly low. The entire data collection attests to the fact that the formation of silicate globules could have been caused by interaction of the conservated fluid and/or water-silicate melt with the host mineral and crystalline inclusions of clinopyroxene and garnet with decreasing pressure during the transportation of grospydite xenoliths by the kimberlite melt to the Earth’s surface.  相似文献   

12.
Mantle xenoliths brought to the surface by kimberlite magmas along the south-western margin of the Kaapvaal craton in South Africa can be subdivided into eclogites sensu stricto, kyanite eclogites and orthopyroxene eclogites, all containing omphacite, and garnet clinopyroxenites and garnet websterites characterised by diopside. Texturally, chemically (major elements) and thermally, we observe an evolution from garnet websterites (TEG = 742–781 °C) towards garnet clinopyroxenites (TEG = 715–830 °C) and to eclogites (TEG = 707–1056 °C, mean value of 913 °C). Pressures calculated for orthopyroxene-bearing samples suggest upper mantle conditions of equilibration (P = 16–33 kb for the garnet websterites, 18 kb for a garnet clinopyroxenite and 23 kb for an opx-bearing eclogite). The overall geochemical similarity between the two groups of xenoliths (omphacite-bearing and diopside-bearing) as well as the similar trace element patterns of clinopyroxenes and garnet suggest a common origin for these rocks. Recently acquired oxygen isotope data on garnet (δ18Ognt = 5.25–6.78 ‰ for eclogites, δ18Ognt = 5.24–7.03 ‰ for garnet clinopyroxenites) yield values ranging from typical mantle values to other interpreted as resulting from low-temperature alteration or precursors sea-floor basalts and associated rocks. These rocks could then represent former magmatic oceanic rocks that crystallised from a same parental magma as plagioclase free diopside-bearing and plagioclase-bearing crustal rocks. During subduction, these oceanic rock protoliths equilibrated at mantle depth, with the plagioclase-bearing rocks converting to omphacite and garnet-bearing lithologies (eclogites sensu largo), whereas the plagioclase-free diopside-bearing rocks converted to diopside and garnet-bearing lithologies (garnet websterites and garnet clinopyroxenites).  相似文献   

13.
Two kimberlite pipes in Elliott County contain rare ultramafic xenoliths and abundant megacrysts of olivine (Fo85–93), garnet (0.21–9.07% Cr2O3), picroilmenite, phlogopite, Cr-poor clinopyroxene (0.56–0.88% Cr2O3), and Cr-poor orthopyroxene (<0.03–0.34% Cr2O3) in a matrix of olivine (Fo88–92), picroilmenite, Cr-spinel, magnetite, perovskite, pyrrhotite, calcite, and hydrous silicates. Rare clinopyroxene-ilmenite intergrowths also occur. Garnets show correlation of mg (0.79–0.86) and CaO (4.54–7.10%) with Cr2O3 content; the more Mg-rich garnets have more uvarovite in solution. Clinopyroxene megacrysts show a general decrease in Cr2O3 and increase in TiO2 (0.38–0.56%) with decreasing mg (0.87–0.91). Clinopyroxene megacrysts are more Cr-rich than clinopyroxene in clinopyroxene-ilmenite intergrowths (0.06–0.38% Cr2O3) and less Cr-rich than peridotite clinopyroxenes (1.39–1.46% Cr2O3). Orthopyroxene megacrysts and orthopyroxene inclusions in olivine megacrysts form two populations: high-Ca, high-Al (1.09–1.16% CaO and 1.16–1.18% Al2O3) and low-Ca, low-Al (0.35–0.46% CaO and 0.67–0.74% Al2O3). Three orthopyroxenes belonging to a low-Ca subgroup of the high-Ca, high-Al group were also identified (0.86–0.98% CaO and 0.95–1.01% Al2O3). The high-Ca, high-Al group (Group I) has lower mg (0.88–0.90) than low-Ca, low-Al group (Group II) with mg=0.92–0.93; low mg orthopyroxenes (Group Ia) have lower Cr2O3 and higher TiO2 than high mg orthopyroxenes (Group II). The orthopyroxene megacrysts have lower Cr2O3 than peridotite orthopyroxenes (0.46–0.57% Cr2O3). Diopside solvus temperatures indicate equilibration of clinopyroxene megacrysts at 1,165°–1,390° C and 1,295°–1,335° C for clinopyroxene in clinopyroxene-ilmenite intergrowths. P-T estimates for orthopyroxene megacrysts are bimodal: high-Ca, high-Al (Group I) orthopyroxenes equilibrated at 1,165°–1,255° C and 51–53 kb (± 5kb) and the low-Ca, low-Al (Group II) orthopyroxenes equilibrated at 970°–1,020°C and 46–56 kb (± 5kb). Garnet peridotites equilibrated at 1,240°–1,360° C and 47–49 kb. Spinel peridotites have discordant temperatures of 720°–835° C (using spinel-olivine Fe/Mg) and 865°–1,125° C (Al in orthopyroxene).Megacrysts probably precipitated from a fractionating liquid at >150 km depth. They are not disaggregated peridotite because: (1) of large crystal size (up to 1.5 cm), (2) compositions are distinctly different from peridotite phases, and (3) they display fractionation trends. The high mg, low T orthopyroxenes and the clustering of olivine rims near Fo89–90 reflect liquid changes to higher MgO contents due to (1) assimilation of wall-rock and/or (2) an increase in Fe3+/Fe2+ and subsequently MgO/FeO as a result of an increase in f o.  相似文献   

14.
Roger H. Mitchell   《Lithos》2004,76(1-4):551-564
Liquidus and sub-liquidus phase relationships are reported for melts formed from an aphanitic kimberlite composition crystallized at 5–12 GPa and 900–1400 °C. The liquidus phase over the pressure range investigated is forsteritic olivine. This is followed with decreasing temperature by olivine plus garnet as the initial sub-liquidus solid phase assemblage. Supra-solidus assemblages consist of olivine+garnet+clinopyroxene+Mg-ilmenite+liquid at 5–7 GPa or olivine+garnet+clinopyroxene+hematite–ilmenite solid solutions (+/−perovskite)+liquid at 8–12 GPa. Phlogopite forms as a near-solidus phase only at 900 °C and 6 GPa. Orthopyroxene does not form at any temperature and pressure. All garnets formed at 6–7 GPa are Ti-rich almandine–grossular–pyrope solid solutions and not Cr-pyrope, whereas garnets formed above 8 GPa are Ti- and Fe3+-rich and have no natural counterparts. Quenched liquids are represented by magnesite at 10–12 GPa and Mg–Ca-carbonates at lower pressures. In addition to forming discrete crystals, Mg-ilmenite and hematite–ilmenite solid solutions occur as lamellar intergrowths that are identical in texture to naturally occurring intergrowths. Mg-ilmenite compositions at 6–7 GPa are similar to those of the natural occurrences, whereas clinopyroxenes are richer in Ca. The effects of graphite versus platinum capsules on the oxygen fugacity of the experimental charges and the composition of the olivine, clinopyroxene, Fe–Ti-oxides and garnets formed are described. These experimental data are interpreted to indicate that kimberlite magmas are unlikely to be formed by very small degrees of partial melting of a simple homogeneous carbonated garnet lherzolite mantle. It is proposed that kimberlite magmas form by extensive partial melting of metasomatized mantle, i.e. mineralogically complex carbonate-bearing veins in a lherzolitic/harzburgitic substrate, and that lamellar ilmenite–clinopyroxene intergrowths represent the products of non-equilibrium growth in kimberlite magma.  相似文献   

15.
Crystalline primary inclusions in diamonds from the Argyle and Ellendale lamproites have been analyzed for Mn, Ni, Cu, Zn, Ga, Pb, Rb, Sr, Y, Zr, Nb, Ta, Ba and Mo by proton microprobe. Eclogite-suite inclusions dominate at Argyle and occur in equal proportions with peridotite-suite inclusions at Ellendale. Eclogitic phases present include garnet, omphacitic clinopyroxene, coesite, rutile, kyanite and sulfide. Eclogitic clinopyroxenes are commonly rich in K and contain 300–1060 ppm Sr and 3–70 ppm Zr: K/Rb increases with K content up to 1400 at 0.7–1.1% K. Rutiles have high Zr and Nb contents with Zr/Nb=1.5–4 and Nb/Ta 16. Of the peridotite-suite inclusions, olivine commonly contains > 10 ppm Sr and Mo; Cr-pyropes are depleted in Sr, Y and Zr, and enriched in Ni, relative to eclogitic garnets.Eclogite-suite diamonds grew in host rocks that were depleted in Mn, Ni and Cr, and enriched in Sr, Zn, Cu, Ga and Ti, relative to Type I eclogite xenoliths from the Roberts Victor Mine. Crystallization temperatures of the eclogite-suite diamonds, as determined by coexisting garnet and clinopyroxene from single diamonds, range from 1085 to 1575° C. Log K D (C i cpx /C i gnt ) varies linearly with 1/T for Zr, Sr and Ga in most of the same samples. This supports the validity of the temperature estimates; Argyle eclogite-suite diamonds have grown over a T range 400° C. Comparison with data from eclogite xenoliths in kimberlites suggests that K D Sr and K D Zr are mainly T-dependent, while K D Ga may be both temperature-and pressuredependent. K D Ni , K D Cu and K D Zn show no T dependence in these samples.In several cases, significant major-and/or trace-element disequilibrium is observed between different grains of the same mineral, or between pyroxene and garnet, within single diamonds. This implies that these diamonds grew in an open system; inclusions trapped at different stages of growth record changes in major and trace-element composition occurring in the host rock. Diamond growth may have been controlled by a fluid flux which introduced or liberated carbon and modified the composition of the rock. The wide range of equilibration temperatures and the range of composition recorded in the inclusions of single diamonds suggest that a significant time interval was involved in diamond growth.  相似文献   

16.
The anhydrous solidus of a natural clinopyroxene-ilmenite intergrowth from the kimberlite pipe at Monastery was found to be 1300° C at 20 kb increasing to 1470 ° C at 47 kb. The slope of the solidus is 6 ° C/kb, with a constant melting interval of approximately 140 ° C. Clinopyroxene was the liquidus phase in all but one case, and the ilmenite-out curve coincided with the beginning of melting. Controlled cooling experiments resulted in liquidus clinopyroxene crystals surrounded by intergrowths of clinopyroxene and ilmenite. The experimental and natural intergrowths are texturally, crystallographically and chemically similar. These results support the view that the natural clinopyroxene-ilmenite intergrowths found in kimberlites are a product of eutectic crystallisation in the upper mantle. Compositional similarities between the liquidus clinopyroxene and discrete clinopyroxene nodules from kimberlite suggest that the latter are possibly related to the clinopyroxene-ilmenite intergrowths by fractional crystallisation. Differences between the temperatures of equilibration obtained for clinopyroxenes from the natural intergrowths, and the beginning of melting on the clinopyroxene-ilmenite join, may be the result of hydrous melting in the former case, or as a consequence of the natural intergrowths existing as mantle veins or pegmatites at the ambient temperature prior to their incorporation in the kimberlite.  相似文献   

17.
We have simulated the dehydration-melting of a natural, low-K, calcic amphibolite (67.4% hornblende, 32.5% anorthite) in piston-cylinder experiments at 10 kbar and 750–1000°C, for 1–9 days. The solidus temperature is lower than 750°C; garnet appears at 850°C. The overall reaction is: Hb+PL+Cpx+Al-Hb+Ca-Hb+Ga+Opx. Three stages of reaction are: (1) melting dominated by the growth of clinopyroxene and garnet, with little change in composition of liquid or garnet, (2) a reversal of this reaction between 875°C and 900°C, with decreases in the amounts of liquid and garnet, and (3) a large increase in liquid along with the loss of hornblende and decrease of plagioclase while clinopyroxene and garnet increase. Garnet is enriched in pyrope and zoned from Fe-cores to Mg-edges (range 3 mol % pyrope); liquid composition is enriched first in An (to 950°C) and then in Ab. The liquids are more calcic and aluminous than natural tonalites, which is attributed to the plagioclase composition (An90). The formation of peraluminous liquid from the metaluminous amphibolite is caused by anorthite — not H2O-saturated conditions. The results are consistent with an amphibolite phase diagram with relatively high solidus temperatures in the garnet-absent field (900–1000°C), but with a solidus backbend at 7–9 kbar, coincident with the garnet-in boundary. Hornblende breakdown due to garnet formation in a closed system must make H2O available for H2O-undersaturated melting right down to the H2O-saturated solidus, below 700°C, which defines a large low-temperature PT area where hydrous granitoid melts can be generated with residual garnet and hornblende.  相似文献   

18.
Geothermometry of eclogites and other high pressure (HP)/ultrahigh‐pressure (UHP) rocks has been a challenge, due to severe problems related to the reliability of the garnet–clinopyroxene Fe–Mg exchange thermometer to omphacite‐bearing assemblages. Likewise, reliable geobarometers for eclogites and related HP/UHP rocks are scarce. In this paper, a set of internally consistent geothermobarometric expressions have been formulated for reactions between the UHP assemblage garnet–clinopyroxene–kyanite–phengite–coesite, and the corresponding HP assemblage garnet–clinopyroxene–kyanite–phengite–quartz. In the system KCMASH, the end members grossular (Grs) and pyrope (Prp) in garnet, diopside (Di) in clinopyroxene, muscovite (Ms) and celadonite (Cel) in phengite together with kyanite and coesite or quartz define invariant points in the coesite and quartz stability field, respectively, depending on which SiO2 polymorph is stable. Thus, a set of net transfer reactions including these end members will uniquely define equilibrium temperatures and pressures for phengite–kyanite–SiO2‐bearing eclogites. Application to relevant eclogites from various localities worldwide show good consistency with petrographic evidence. Eclogites containing either coesite or polycrystalline quartz after coesite all plot within the coesite stability field, while typical quartz‐bearing eclogites with no evidence of former coesite fall within the quartz stability field. Diamondiferous coesite–kyanite eclogite and grospydite xenoliths in kimberlites all fall into the diamond stability field. The present method also yields consistent values as compared with the garnet–clinopyroxene Fe–Mg geothermometer for these kinds of rocks, but also indicates some unsystematic scatter of the latter thermometer. The net transfer geothermobarometric method presented in this paper is suggested to be less affected by later thermal re‐equilibration than common cation exchange thermometers.  相似文献   

19.
Isobaric partial melting experiments were performed on an Fe-free synthetic composition to simulate partial melting of subducted oceanic crust. Nominally anhydrous experiments at 3.0 GPa yielded melts in equilibrium with garnet (13 to 16 mol.% grossular) and aluminous clinopyroxene (14 to 16 wt.% Al2O3). Melt compositions show decreasing Si and alkalis and increasing Ca, Mg, and Ti contents with increasing temperatures. Experiments at 1200 and 1300°C were rutile saturated, whereas experiments at 1400°C contained no residual rutile. We argue that during the initial stages of subduction, accessory rutile is likely to be stable in subsolidus eclogites of average midocean ridge basalt composition and that only large degrees of partial melting will eradicate rutile from an eclogitic source. At 3 GPa, any eclogites with a bulk TiO2 content of ≥1.5 wt.% rutile will produce rutile-saturated partial melts, except at very high degrees of melting. At higher pressures, all bulk Ti may dissolve in clinopyroxene and garnet, leaving no accessory rutile.Trace element partition coefficients for 24 trace elements between clinopyroxene, garnet, and melt were determined by secondary-ion mass spectrometry analysis of experimental run products at 1400°C and 3 GPa. Partition coefficients for the rare earth elements agree well with previous studies and have been evaluated using the lattice strain model. Partitioning data for high-field strength elements indicate complementary DZr/DHf for clinopyroxene and garnet. Partial melting of an eclogitic component of different modal compositions may therefore explain both subchondritic and superchondritic Zr/Hf ratios. Superchondritic Zr/Hf has recently been observed in some ocean island basalts (OIB), and this may be taken as further evidence for components of recycled oceanic crust in OIB. The data also indicate slight Nb/Ta fractionation during partial melting of bimineralic eclogite, which is not, however, sufficient to explain some recently observed Nb/Ta fractionation in island arc rocks. Accessory rutile, however, can explain such fractionation.  相似文献   

20.
Basic inclusions of two types occur in a kimberlitic diatreme at Kayrunnera in northwestern New South Wales. Type I inclusions comprise assemblages of clinopyroxene+garnet+rutile±plagioclase ±quartz±K-feldspar±scapolite±sphene±apaite. Type II inclusions have assemblages of clinopyroxene +garnet+kyanite+quartz±plagioclase and are lower in Ti, total Fe, and higher in Al and have a higher Mg/Mg+gSFe ratio than the Type I inclusions. Experimental and theoretical data indicate that both inclusion types equilibrated at between 850–900 ° C and 18–23 kb. Due to their low concentrations of incompatible elements, the Type I inclusions are considered to represent a basaltic melt derived from an Fe-rich mantle source rock, and not to be the product of fractionation. The Type II inclusions are believed to represent cumulates which formed from a basaltic magma. The presence of sulphur rich scapolite in the Type I inclusions extends the range of P-T conditions from which this mineral has been reported thus adding further credence to the hypothesis that it may act as a stable repository for S and CO2 in the crust and upper mantle.  相似文献   

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