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1.
沙茜  周永胜 《岩石学报》2018,34(3):851-865
本文在高温高压条件下,开展了辉长岩矿物反应与部分熔融实验,利用偏光显微镜与扫描电镜对实验样品微观结构观察,研究实验中的新生矿物与熔体的分布;通过电子探针分析熔体成分特征。实验结果表明,在低压(300MPa)条件下,静压和塑性变形实验样品中,单斜辉石以固体反应方式生成橄榄石,在高压(1300MPa)塑性实验中所有实验样品都没有发现新生矿物颗粒,这与相图中低压条件下斜长石与橄榄石稳定共存,而高压下斜长石-辉石稳定共存相吻合。高压塑性变形条件下,单斜辉石和黑云母首先发生部分熔融,随着温度增高,斜长石逐渐参与熔融,熔体呈薄膜状分布在矿物颗粒边界,熔体成分依赖于参与熔融的矿物成分,表明出现的熔体为非平衡熔融结果。  相似文献   

2.
The ternary feldspar system KAlSi3O8 - NaAlSi3O8 - CaAl2Si2O8 was reinvestigated at 650 ° C and 800 ° C (P H2O = 1 kb) using mixtures of crystalline plagioclases and alkali feldspars as starting materials. The compositions of plagioclases and alkali feldspars of the run products were determined by X-ray means. The Or-content of the feldspar phases was determined by measuring the position of the (201) X-ray peak of the unexchanged feldspars, whereas the An-content was determined by measuring the same X-ray peak of the K-exchanged feldspars. The reaction rate of a reaction leading to a more An-rich plagioclase (type II reaction) is much faster than a reaction producing a more Ab-rich plagioclase (type I). In a type II reaction run times of approximately 20 days are needed to reach new constant plagioclase and alkali feldspar compositions at 650 ° C, and 10 days are needed to reach constant compositions at 800 ° C. In a reaction of type I only the outer zone of the plagioclases reacts to more Abrich compositions. A diffuse zone with a wide range of compositions was observed in 650 ° C runs. Equilibrium could not be reached in these experiments within 45 days. At 800 ° C a new zone having a specific composition develops in 42 days. This new zone is believed to be in equilibrium with the coexisting alkali feldspar. The depth of reaction is calculated as 0.03 μm after 42 days (800 ° C, P f= 1 kb). The reaction between the two feldspar phases could be reversed at 800 ° C. The following compositions are considered to represent equilibrium data at 800 ° C and P t = 1 kb:
  • An 43 Ab 51 Or 6 coexisting with Or 79 Ab 20 An 1, and
  • An 40 Ab 54 Or 6 coexisting with Or 75 Ab 24 An 1.
    • Recent data obtained with gels of ternary feldspar composition as starting materials do not agree with the results presented in this paper. Gels obviously crystallize spontaneously forming coexisting feldspars of non - equilibrium composition - alkali feldspars too rich in Ab and plagioclases too rich in An.  相似文献   

    3.
    Dehydration melting of tonalites. Part II. Composition of melts and solids   总被引：6，自引：0，他引：6  
     Dehydration melting of tonalitic compositions (phlogopite or biotite-plagioclase-quartz assemblages) is investigated within a temperature range of 700–1000°C and pressure range of 2–15 kbar. The solid reaction products in the case of the phlogopite-plagioclase(An45)-quartz starting material are enstatite, clinopyroxene and potassium feldspar, with amphiboles occurring occasionally. At 12 kbar, zoisite is observed below 800°C, and garnet at 900°C. The reaction products of dehydration melting of the biotite (Ann50)-plagioclase (An45)-quartz assemblage are melt, orthopyroxene, clinopyroxene, amphibole and potassium feldspar. At pressures > 8 kbar and temperatures below 800°C, epidote is also formed. Almandine-rich garnet appears above 10 kbar at temperatures ≥ 750°C. The composition of melts is granitic to granodioritic, hence showing the importance of dehydration melting of tonalites for the formation of granitic melts and granulitic restites at pressure-temperature conditions within the continental crust. The melt compositions plot close to the cotectic line dividing the liquidus surfaces between quartz and potassium feldspar in the haplogranite system at 5 kbar and a H 2O = 1. The composition of the melts changes with the composition of the starting material, temperature and pressure. With increasing temperature, the melt becomes enriched in Al2O3 and FeO+MgO. Potash in the melt is highest just when biotite disappears. The amount of CaO decreases up to 900°C at 5 kbar whereas at higher temperatures it increases as amphibole, clinopyroxene and more An-component dissolve in the melt. The Na2O content of the melt increases slightly with increase in temperature. The composition of the melt at temperatures > 900°C approaches that of the starting assemblage. The melt fraction varies with composition and proportion of hydrous phases in the starting composition as well as temperature and pressure. With increasing modal biotite from 20 to 30 wt%, the melt proportion increases from 19.8 to 22.3 vol.% (850°C and 5 kbar). With increasing temperature from 800 to 950°C (at 5 kbar), the increase in melt fraction is from 11 to 25.8 vol.%. The effect of pressure on the melt fraction is observed to be relatively small and the melt proportion in the same assemblage decreases at 850°C from 19.8 vol.% at 5 kbar to 15.3 vol.% at 15 kbar. Selected experiments were reversed at 2 and 5 kbar to demonstrate that near equilibrium compositions were obtained in runs of longer duration. Received: 27 December 1995 / Accepted: 7 May 1996  相似文献   

    4.
    A spinel lherzolite body outcrops as a fault block on the north coast of East Timor. The most common rock‐type in this body is a clinopyroxene‐poor lherzolite, but there are smaller proportions of clinopyroxene‐rich lherzolite and harzburgite. The dominant mineral assemblage is olivine, orthopyroxene, clinopyroxene, spinel and calcic amphibole. Low‐temperature hydrous minerals are restricted in distribution.

    The chemical composition of the peridotite is closely similar to mantle‐derived spinel lherzolite nodules and some alpine peridotites. The internal variation of the peridotite suggests variable depletion by some combination of partial melting and liquid contamination of the residua, in a CO2‐rich system at 10–15 kb (1000–1500 MPa).

    Three solid‐state events are indicated by geothermometry. The earliest event is recorded by coarse exsolution lamellae of orthopyroxene in clinopyroxene porphyro‐clasts. These grains formed at 1250°C. A later granoblastic texture equilibrated at 1100°C, and finally the rocks were mylonitised at 800–1000°C and 8–20 kb (800–2000 MPa).

    The peridotite is probably a sample of the oceanic mantle trapped between the Java Trench and the Inner Banda Arc. Its emplacement on Timor is not related to obduction, but may be due to transcurrent faulting between the Asian and Australian plates.  相似文献   

    5.
     The beginning of dehydration melting in the tonalite system (biotite-plagioclase-quartz) is investigated in the pressure range of 2–12 kbar. A special method consisting of surrounding a crystal of natural plagioclase (An45) with a biotite-quartz mixture, and observing reactions at the plagioclase margin was employed for precise determination of the solidus for dehydration melting. The beginning of dehydration melting was worked out at 5 kbar for a range of compositions of biotite varying from iron-free phlogopite to iron-rich Ann70, with and without titanium, fluorine and extra aluminium in the biotite. The dehydration melting of phlogopite + plagioclase (An45) + quartz begins between 750 and 770°C at pressures of 2 and 5 kbar, at approximately 740°C at 8 kbar and between 700 and 730°C at 10 kbar. At 12 kbar, the first melts are observed at temperatures as low as 700°C. The data indicate an almost vertical dehydration melting solidus curve at low pressures which bends backward to lower temperatures at higher pressures (> 5 kbar). The new phases observed at pressures ≤ 10 kbar are melt + enstatite + clinopyroxene + potassium feldspar ± amphibole. In addition to these, zoisite was also observed at 12 kbar. With increasing temperature, phlogopite becomes enriched in aluminium and deficient in potassium. Substitution of octahedral magnesium by aluminium and titanium in the phlogopite, as well as substitution of hydroxyl by fluorine, have little effect on the beginning of dehydration melting temperatures in this system. The dehydration melting of biotite (Ann50) + plagioclase (An45) + quartz begins 50°C below that of phlogopite bearing starting composition. Solid reaction products are orthopyroxene + clinopyroxene + potassium feldspar ± amphibole. Epidote was also observed above 8 kbar, and garnet at 12 kbar (750°C). The experiments on the iron-bearing system performed at ≤ 5 kbar were buffered with NiNiO. The f O 2 in high pressure runs lies close to CoCoO. With the substitution of octahedral magnesium and iron by aluminium and titanium, and replacement of hydroxyl by fluorine in biotite, the beginning of dehydration melting temperatures in this system increase up to 780°C at 5 kbar, which is 70°C above the beginning of dehydration melting of the assemblage containing biotite (Ann50) of ideal composition. The dehydration melting at 5 kbar in the more iron-rich Ann70-bearing starting composition begins at 730°C, and in the Ann25-bearing assemblage at 710°C. This indicates that quartz-biotite-plagioclase assemblages with intermediate compositions of biotite (Ann25 and Ann50) melt at lower temperatures as compared to those containing Fe-richer or Mg-richer biotites. This study shows that the dehydration melting of tonalites may begin at considerably lower temperatures than previously thought, especially at high pressures (>5 kbar). Received: 27 December 1995 / Accepted: 7 May 1996  相似文献   

    6.
    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   

    7.
    The textures and kinetics of reaction between plagioclase and melts have been investigated experimentally, and origin of dusty plagioclase in andesites has been discussed. In the experiments plagioclase of different compositions (An96, An61, An54, An23, and An22) surrounded by glasses of six different compositions in the system diopside-albite-anorthite was heated at temperatures ranging from 1,200 to 1,410° C for 30 min to 88 h. Textures were closely related to temperature and chemical compositions. A crystal became smaller and rounded above the plagioclase liquidus temperature of the starting melt (glass) and remained its original euhedral shape below the liquidus. Whatever the temperature, the crystal-melt interface became rough and often more complicated (sieve-like texture composed of plagioclase-melt mixture in the scale of a few m was developed from the surface of the crystal inward; formation of mantled plagioclase) if the crystal is less calcic than the plagioclase in equilibrium with the surrounding melt, and the interface remained smooth if the crystal is more calcic than the equilibrium plagioclase. From these results the following two types of dissolution have been recognized; (1) a crystal simply dissolves in the melt which is undersaturated with respect to the phase (simple dissolution), and a crystal is partially dissolved to form mantled plagioclase by reaction between sodic plagioclase and calcic melt (partial dissolution). The amount of a crystal dissolved and reacted increased proportional to the square root of time. This suggests that these processes are controlled by diffusion, probably in the crystal.Mantled plagioclase produced in the experiments were very similar both texturally and chemically to some of the so-called resorbed plagioclase in igneous rocks. Chemical compositions and textures of plagioclase phenocrysts in island-arc andesites of magma mixing origin have been examined. Cores of clear and dusty plagioclase were clacic (about An90) and sodic (about An50), respectively. This result indicates that dusty plagioclases were formed by the partial melting due to reaction between sodic plagioclase already precipitated in a dacitic magma and a melt of intermediate composition in a mixed magma during the magma mixing.  相似文献   

    8.
    Partial melting of continental crust and evolution of granitic magmas are inseparably linked to the availability of H2O. In the absence of a free aqueous fluid, melting takes place at relatively high temperatures by dehydration of hydrous minerals, whereas in its presence, melting temperatures are lowered, and melting need not involve hydrous minerals. With the exception of anatexis in water‐saturated environments where anhydrous peritectic minerals are absent, there is no reliable indicator that clearly identifies the presence of a free aqueous fluid during anatexis. Production of Ab‐rich magmas or changes in LILE ratios, such as an increase in Sr and decrease in Rb indicating increased involvement of plagioclase, are rough guidelines to the presence of aqueous fluids. Nevertheless, all indicators have caveats and cannot be unequivocally applied, allowing for the persistence of a bias in the literature towards dehydration melting. Investigation of mineral equilibria modelling of three metasedimentary protoliths of the Kangaroo Island migmatites in South Australia, shows that the main indicator for the presence of small volumes of excess water under upper amphibolite to lower granulite facies conditions (660–750°C) is the melt volume produced. Melt composition, modal content or chemical composition of peritectic minerals such as cordierite, sillimanite or garnet are relatively insensitive to the presence of free water. However, the mobility of melt during open system behaviour makes it difficult to determine the melt volume produced. We therefore argue that the presence of small volumes of excess water might be much more common than so far inferred, with large impact on the buffering of crustal temperatures and fertility, and therefore rheology of the continental crust.  相似文献   

    9.
    Partial melting of metagreywackes, Part II. Compositions of minerals and melts   总被引：16，自引：0，他引：16  
    A series of experiments on the fluid-absent melting of a quartz-rich aluminous metagreywacke has been carried out. In this paper, we report the chemical composition of the phases present in the experimental charges as determined by electron microprobe. This analytical work includes biotite, plagioclase, orthopyroxene, garnet, cordierite, hercynite, staurolite, gedrite, oxide, and glass, over the range 100–1000 MPa, 780–1025 °C. Biotites are Na- and Mg-rich, with Ti contents increasing with temperature. The compositions of plagioclase range from An17 to An35, with a significant orthoclase component, and are always different from the starting minerals. At high temperature, plagioclase crystals correspond to ternary feldspars with Or contents in the range 11–20 mol%. Garnets are almandine pyrope grossular spessartine solid solutions, with a regular and significant increase of the grossular content with pressure. All glasses are silicic (SiO2 = 67.6–74.4 wt%), peraluminous, and leucocratic (FeO + MgO = 0.9–2.9 wt%), with a bulk composition close to that of peraluminous leucogranites, even for degrees of melting as high as 60 vol.%. With increasing pressure, SiO2 contents decrease while K2O increases. At any pressure, the melt compositions are more potassic than the water-saturated granitic minima. The H2O contents estimated by mass balance are in the range 2.5–5.6 wt%. These values are higher than those predicted by thermodynamic models. Modal compositions were estimated by mass balance calculations and by image processing of the SEM photographs. The positions of the 20 to 70% isotects (curves of equal proportion of melt) have been located in the pressure-temperature space between 100 MPa and 1000 MPa. With increasing pressure, the isotects shift toward lower temperature between 100 and 200 MPa, then bend back toward higher temperature. The melting interval increases with pressure; the difference in temperature between the 20% and the 70% isotects is 40 °C at 100 MPa, and 150 °C at 800 MPa. The position of the isotects is interpreted in terms of both the solubility of water in the melt and the nature of the reactions involved in the melting process. A comparison with other partial melting experiments suggests that pelites are the most fertile source rocks above 800 MPa. The difference in fertility between pelites and greywackes decreases with decreasing pressure. A review of the glass compositions obtained in experimental studies demonstrates that partial melting of fertile rock types in the crust (greywackes, pelites, or orthogneisses) produces only peraluminous leucogranites. More mafic granitic compositions such as the various types of calk-alkaline rocks, or mafic S-type rocks, have never been obtained during partial melting experiments. Thus, only peraluminous leucogranites may correspond to liquids directly formed by partial melting of metasediments. Other types of granites involve other components or processes, such as restite unmixing from the source region, and/or interaction with mafic mantle-derived materials. Received: 11 July 1995 / Accepted: 27 February 1997  相似文献   

    10.
    In the North‐East Greenland Caledonides, P–T conditions and textures are consistent with partial melting of ultrahigh‐pressure (UHP) eclogite during exhumation. The eclogite contains a peak assemblage of garnet, omphacite, kyanite, coesite, rutile, and clinozoisite; in addition, phengite is inferred to have been present at peak conditions. An isochemical phase equilibrium diagram, along with garnet isopleths, constrains peak P–T conditions to be subsolidus at 3.4 GPa and 940°C. Zr‐in‐rutile thermometry on inclusions in garnet yields values of ~820°C at 3.4 GPa. In the eclogite, plagioclase may exhibit cuspate textures against surrounding omphacite and has low dihedral angles in plagioclase–clinopyroxene–garnet aggregates, features that are consistent with former melt–solid–solid boundaries and crystallized melt pockets. Graphic intergrowths of plagioclase and amphibole are present in the matrix. Small euhedral neoblasts of garnet against plagioclase are interpreted as formed from a peritectic reaction during partial melting. Polymineralic inclusions of albite+K‐feldspar and clinopyroxene+quartz±kyanite±plagioclase in large anhedral garnet display plagioclase cusps pointing into the host, which are interpreted as crystallized melt pockets. These textures, along with the mineral composition, suggest partial melting of the eclogite by reactions involving phengite and, to a large extent, an epidote‐group mineral. Calculated and experimentally determined phase relations from the literature reveal that partial melting occurred on the exhumation path, at pressures below the coesite to quartz transition. A calculated P–T phase diagram for a former melt‐bearing domain shows that the formation of the peritectic garnet rim occurred at 1.4 GPa and 900°C, with an assemblage of clinopyroxene, amphibole, and plagioclase equilibrated at 1.3 GPa and 720°C. Isochemical phase equilibrium modelling of a symplectite of clinopyroxene, plagioclase, and amphibole after omphacite, combined with the mineral composition, yields a P–T range at 1.0–1. 6 GPa, 680–1,000°C. The assemblage of amphibole and plagioclase is estimated to reach equilibrium at 717–732°C, calculated by amphibole–plagioclase thermometry for the former melt‐bearing domain and symplectite respectively. The results of this study demonstrate that partial melt formed in the UHP eclogite through breakdown of an epidote‐group mineral with minor involvement of phengite during exhumation from peak pressure; melt was subsequently crystallized on the cooling path.  相似文献   

    11.
    Several intrusions of ultrabasic to basic composition occur in the Roslagen area of east‐central Sweden in close spatial and temporal association with the surrounding 1.90–1.87 Ga old early orogenic Svecofennian granitoids. An imprecise Sm‐Nd WR errorchron yields an age of 1895 ± 71 Ma. In spite of the penetrative deformation in the granitoids, the basic–ultrabasic rocks mostly appear undeformed and largely preserve magmatic textures with plagioclase, olivine (in some rock types), orthopyroxene and clinopyroxene, and amphibole as major constituents. The plagioclase is typically very anorthitic (ca. An90). The Roslagen intrusions range in composition from primitive to evolved (Mg# 80 to 49) but contain only 40–50 wt% SiO2. Many samples are highly elevated in Al2O3 (up to 30 wt%), CaO (up to 16 wt%) and Sr (up to 800 ppm), with strongly positive Eu and Sr anomalies, in line with being plagioclase cumulates. Although masked by cumulus effects, the relative trace element contents indicate a volcanic arc signature. The initial Nd isotope composition is homogeneously ‘mildly depleted’, with εNd of +0.3 to +1.1, and the initial Sr isotope composition ‘mildly enriched’, with εSr of +8 to +15. Non‐cumulus rocks with small Eu and Sr anomalies can be used to deduce the composition of the parental magma. This LILE‐ and LREE‐enriched and HFSE‐depleted high‐alumina basalt magma, with Mg# of ca. 50–60 and Ca# of ca. 80, most likely formed by partial melting of mantle material, enriched by fluids in a subduction environment, at 1.9 Ga. The cumulate rocks apparently crystallized from a somewhat more evolved water‐rich magma with Mg# of ca. 40. Crystallization was followed by the development of late‐magmatic to post‐magmatic coronas between olivine and plagioclase in the presence of H2O‐rich fluids. The subduction‐related setting would make these intrusions Palaeoproterozoic counterparts of Alaskan‐type ultramafic intrusions, but they differ from those in being plagioclase enriched, possibly reflecting different levels of exposure. Copyright © 2012 John Wiley & Sons, Ltd.  相似文献   

    12.
    Monazite is a common accessory phase in felsic granulite ribbon mylonites exposed in the Upper Deck domain of the Athabasca granulite terrane, western Canadian Shield. Field relationships, bulk rock geochemistry and phase equilibria modelling in the Na2O–CaO–K2O–FeO–MgO–Al2O3–SiO2–H2O–TiO2–Fe2O3 system are consistent with the garnet‐rich rocks representing the residual products of ultrahigh temperature melting of biotite‐bearing paragneisses driven by intraplating of mafic magma in continental lower crust. The c. 2.64–2.61 Ga Y‐rich resorbed monazite cores included in garnet are interpreted as relicts of detrital grains deposited on the Earth's surface after c. 2.61 Ga. Yttrium‐poor monazite domains in garnet are depleted in Sm and Gd and linked to fluid‐absent melting of biotite + plagioclase + quartz ± sillimanite during a prograde loading path from ≤0.8 to ≥1.4 GPa. The c. 2.61–2.55 Ga Y‐depleted, Th‐rich monazite domains crystallized in the presence of garnet + ternary feldspar ± orthopyroxene + peraluminous melt. The c. 2.58–2.52 Ga monazite rims depleted in Th + Ca and enriched in Eu are linked to localized melt extraction synchronous with growth of high‐pressure (HP) grossular‐rich garnet at the expense of plagioclase during crustal thickening, culminating at >950 °C. Re‐heating and dextral transpressive lower crustal reactivation at c. 1.9 Ga resulted in syn‐kinematic growth of (La + Ce)‐enriched monazite and a second generation of garnet, concurrent with recrystallization of feldspar and orthopyroxene at 1.0–1.2 GPa and 600–700 °C. Monazite grains in this study are marked by positive Eu‐anomalies relative to chondrite. A direct link is implied between Y, Sm, Eu and Gd in monazite and two major phases in continental lower crust: garnet and plagioclase. Positive Eu‐anomalies in lower crustal monazite associated with modally abundant garnet appear to be directly related to Eu‐enrichment and depletions of Y, Sm and Gd that are consequences of garnet growth and plagioclase breakdown during HP melting of peraluminous bulk compositions.  相似文献   

    13.
    Spectacular shallow-level migmatization of ferrogabbroic rocks occurs in a metamorphic contact aureole of a gabbroic pluton of the Tierra Mala massif (TM) on Fuerteventura (Canary Islands). In order to improve our knowledge of the low pressure melting behavior of gabbroic rocks and to constrain the conditions of migmatization of the TM gabbros, we performed partial melting experiments on a natural ferrogabbro, which is assumed as protolith of the migmatites. The experiments were performed in an internally heated pressure vessel (IHPV) at 200 MPa, 930–1150 °C at relatively oxidizing conditions. Distinct amounts of water were added to the charge.

    From 930 to 1000 °C, the observed experimental phases are plagioclase (An60–70), clinopyroxene, amphibole (titanian magnesiohastingsites), two Fe–Ti oxides, and a basaltic, K-poor melt. Above 1000 °C, amphibole is no longer stable. The first melts are very rich in normative plagioclase (>70 wt.%). This indicates that at the beginning of partial melting plagioclase is the major phase which is consumed to produce melt. In the experiments, plagioclase is stable up to high temperatures (1060 °C) showing increasing An content with temperature. This is not compatible with the natural migmatites, in which An-rich plagioclase is absent in the melanosomes, while amphibole is stable. Our results show that the partial melting of the natural rocks cannot be regarded as an “in-situ” process that occurred in a closed system. Considerable amounts of alkalis probably transported by water-rich fluids, derived from the mafic pluton underplating the TM gabbro, were necessary to drive the melting reaction out of the stability range of plagioclase. A partial melting experiment with a migmatite gabbro showing typical “in-situ” textures as starting material supports this assumption.

    Crystallization experiments performed at 1000 °C on a glass of the fused ferrogabbro with different water contents added to the charge show that generally high water activities could be achieved (crystallization of amphibole), independently of the bulk water content, even in a system with very low initial bulk water content (0.3 wt.%). Increasing water contents produce plagioclase richer in An, reduces the modal proportion of plagioclase in the crystallizing assemblage and extends the melt fraction. High melt fractions of >30 wt.% could only be observed in systems with high bulk water contents (>2 wt.%). This indicates that the migmatites were generated under water-rich conditions (probably water-saturated), since those migmatites, which are characterized as “in-situ” formations, show generally high amounts of leucosomes (>30 wt.%).  相似文献   


    14.
    The melting of plagioclase and quartz has been investigated at P H2O =2kb. A single crystal of plagioclase was surrounded by quartz powder and water. A reaction rim consisting of glass and of An-rich plagioclase developed around unchanged starting plagioclase. Microprobe determinations of melt and coexisting plagioclase compositions reveal a strong fractionation of plagioclase components between melt and new plagioclase. For example at 850° C the approximate X An of melt is 0.3 and that of plagioclase is 0.8. The temperature interval between beginning of melting and complete melting of cotectic compositions is 100° C or more for quartz-plagioclase mixtures with plagioclases between An 40 and An 75. In comparison to the system Ab-An-H2O the plagioclase melting loop is somewhat wider in the investigated system Qz-Ab-An-H2O but the temperature interval is much smaller (100° C) than in the system Ab-An-H2O (200° C). The solidus data indicated by the new plagioclase compositions are practically identical with those observed in beginning of melting experiments. The results show that fractionation of plagioclase components between partial melts and restite plagioclase can be more pronounced in multi-component rocks than in the pure plagioclase system. This finding is important for the development of albite rich rocks from more basic compositions.  相似文献   

    15.
    Orthopyroxene‐free garnet + clinopyroxene + plagioclase ± quartz‐bearing mineral assemblages represent the paragenetic link between plagioclase‐free eclogite facies metabasites and orthopyroxene‐bearing granulite facies metabasites. Although these assemblages are most commonly developed under P–T conditions consistent with high pressure granulite facies, they sometimes occur at lower grade in the amphibolite facies. Thus, these assemblages are characteristic but not definitive of high pressure granulite facies. Compositional factors favouring their development at amphibolite grade include Fe‐rich mineral compositions, Ca‐rich garnet and plagioclase, and Ti‐poor hornblende. The generalized reaction that accounts for the prograde development of garnet + clinopyroxene + plagioclase ± quartz from a hornblende + plagioclase + quartz‐bearing (amphibolite) precursor is Hbl + Pl + Qtz=Grt + Cpx + liquid or vapour, depending on whether the reaction occurs above or below the solidus. There are significant discrepancies between experimental and natural constraints on the P–T conditions of orthopyroxene‐free garnet + clinopyroxene + plagioclase ± quartz‐bearing mineral assemblages and therefore on the P–T position of this reaction. Semi‐quantitative thermodynamic modelling of this reaction is hampered by the lack of a melt model and gives results that are only moderately successful in rationalizing the natural and experimental data.  相似文献   

    16.
    Plagioclase-aqueous solution equilibrium: Concentration dependence   总被引：1，自引：0，他引：1  
    The plagioclase-(NaCl + CaCl2) exchange equilibrium was examined experimentally at 700°C, 0.5 GPa in aqueous solutions with salt concentrations from 1 to 64 m. The Ca/(Ca + Na) distribution between plagioclase and solution (salt melt) is illustrated in five diagrams constructed for concentrations of 1, 4, 8, 16, and 64 m. The elevated bulk salinity of the fluid at a constant Ca/(Ca + Na) ratio results in plagioclase albitization, with this effect reaching a maximum in relatively dilute solutions (1–4 m). In concentrated solutions (salt melts), the shift in the plagioclase composition with variations in the salinity is relatively insignificant. The simple hydration of basic rocks (purely metamorphic reaction) is associated with the albitization of plagioclase, and calculations suggest a possible shift from anorthite to oligoclase. This is also applicable to chemically more complex mineral associations: an increase in the overall salinity of the fluid should result in an increase in the activity of monovalent cations relative to that of bivalent ones and, correspondingly, stimulate reactions in which alkali earth cations (Ca + Mg + Fe) are substituted for alkalis (Na + K + Li). Although our experiments were carried out at temperatures 50°C lower than the melting point of albite under a pure water pressure (0.5 GPa), the addition of CaCl2 solution to albite (i.e., plagioclase anorthitization and a decrease in the water activity in the salt solutions) induced the appearance of melt because of quartz formation by the reaction 2Ab + CaCl2 → An + 2NaCl + 4Qtz and the eutectic phase proportions in the Ab + Qtz system.  相似文献   

    17.
    The submarine volcanoes, located in the southern part of Andaman Sea, north eastern Indian Ocean, result from the subduction of the Indo-Australian Plate beneath the Southeast Asian Plate and represent one of the less studied submarine volcanism among the global arc systems. The present study provides new petrological and geochemical data for the recovered rocks from the submarine volcanoes and documents the petrogenetic evolution of Andaman arc system. Geochemical attributes classify the studied samples as basaltic andesite, andesite, dacite to rhyodacite reflecting sub-alkaline, intermediate to acidic composition of the magma. Petrographic studies of the basaltic andesites and andesites show plagioclase [An38-An57 in basaltic andesites; An27-An28 in andesites] and clinopyroxene as dominant phenocrystal phase in a cryptocrystalline groundmass. Plagioclase (An25-An45) marks the principal phenocrystal phase in dacite with sub-ordinate proportion of biotite and amphibole of both primary and secondary origin along with minor amount of K-feldspar. The submarine volcanic rocks from Andaman arc system exhibit pronounced LILE, LREE enrichments and HFSE (negative Nb, Ta and Ti anomalies), MREE and HREE depletion thereby endorsing the influence of subduction zone processes in their genesis. Elevated abundances of Th with relatively higher LREE/HFSE than LILE/HFSE, LILE/LREE suggest significant contribution of sediments from the subducting slab over slab-dehydrated aqueous fluids towards mantle wedge metasomatism thereby modifying the sub-arc mantle. Partial melting curves calculated using the non-modal batch melting equation suggest primary magma generated due to ~31–35 % degree of partial melting of spinel lherzolite mantle beneath the arc system. Fractional crystallization model suggests fractionation of 45 % plagioclase, 40 % clinopyroxene, 5–10 % amphibole and 5–10 % biotite which is consistent with the petrographic observations. Further, the assimilation-fractional-crystallization (AFC) model for the studied rocks indicates nominal crustal contamination. Therefore, this study infers that the melt evolution history for the Andaman arc volcanic rocks can be translated in terms of (i) generation of precursor magma by ~31–35 % partial melting of a spinel lherzolite mantle wedge, metasomatized predominantly by subducted slab sediments and (ii) the parent magma generation was ensued by fractionation dominated melt differentiation with nominal input from arc crust.  相似文献   

    18.
    Permian‐aged metagabbros from the eclogite type‐locality in the eastern European Alps were partially to completely transformed to eclogite during Eoalpine intracontinental subduction. Microtextures developed along a preserved fluid infiltration and reaction front in the gabbros record the incipient gabbro‐to‐eclogite transition, allowing the details of the eclogitization process to be investigated. Original, anorthite‐rich igneous plagioclase is pervasively replaced by fine‐grained intergrowths of clinozoisite, kyanite and Na‐rich plagioclase. Where plagioclase was in contact with igneous orthopyroxene, 100–200 μm thick bimineralic coronae of symplectic kyanite and diopsidic clinopyroxene form along the edges of the grains. The rims of igneous orthopyroxene develop a complementary bimineralic corona of diopsidic clinopyroxene and garnet. Igneous clinopyroxene does not show any breakdown textures; however, jadeite content gradually increases towards the rims. In addition, exsolution lamellae inherited from the igneous clinopyroxene become progressively more jadeitic as eclogitization proceeds. Given that the igneous plagioclase is pervasively replaced by clinozoisite, kyanite and Na‐rich plagioclase, whereas kyanite–diopside symplectites are confined to narrow rim zones, we suggest that the development of these textures was controlled by the (im)mobility of different elements on different length scales. The presence of hydrous minerals in the core of anhydrous plagioclase indicates that H2O diffusivity occurred on a mm‐scale. By contrast, the size of the anhydrous diopside–kyanite and diopside–garnet symplectites indicate that Fe–Mg–Ca–Na diffusivity was limited to a 10s of μm scale. Chemical potential relations calculated in the idealized NCASH chemical system show that the clinozoisite–kyanite–albite intergrowths formed due to an increase of μH2O to plagioclase, whereas all other elements remained effectively immobile on the scale of this texture. Fluid conditions indicated by this texture span from virtually dry conditions (0.15) to H2O‐saturation, and therefore does not imply that the rocks were ever fluid‐saturated. Calculations in the CMAS and NCFMAS systems show that the gabbro‐to‐eclogite transition is characterized by the growth of garnet, diopsidic clinopyroxene and kyanite due to diffusion of Ca (+ Na) and Mg (+ Fe) along a μCaO (+ Na2O)–μMgO (+ FeO) chemical potential gradient developed between orthopyroxene and plagioclase compositional domains. The anhydrous nature of the textures indicate that the gabbro‐to‐eclogite transition is not driven by hydration; however, increased μH2O acts as a catalyst that increases diffusivity of all elements and rates of dissolution–precipitation, allowing the overstepped metamorphic reactions to occur. Our results show that crustal eclogite formation requires low H2O content, confirming that true eclogites are dry rocks.  相似文献   

    19.
    Biotite + plagioclase + quartz (BPQ) is a common assemblagein gneisses, metasediments and metamorphosed granitic to granodioriticintrusions. Melting experiments on an assemblage consistingof 24 vol. % quartz, 25 vol. % biotite (XMg = 0·38–0·40),42 vol. % plagioclase (An26–29), 9 vol. % alkali feldsparand minor apatite, titanite and epidote were conducted at 10,15 and 20 kbar between 800 and 900°C under fluid-absentconditions and with small amounts (2 and 4 wt %) of water addedto the system. At 10 kbar when 4 wt % of water was added tothe system the biotite melting reaction occurred below 800°Cand produced garnet + amphibole + melt. At 15 kbar the meltingreaction produced garnet + amphibole + melt with 2 wt % addedwater. At 20 kbar the amphibole occurred only at high temperature(900°C) and with 4 wt % added water. In this last case themelting reaction produced amphibole + clinopyroxene ±garnet + melt. Under fluid-absent conditions the melting reactionproduced garnet + plagioclase II + melt and left behind a plagioclaseI ± quartz residuum, with an increase in the modal amountof garnet with increasing pressure. The results show that itis not possible to generate hornblende in such compositionswithout the addition of at least 2–4 wt % H2O. This reflectsthe fact that conditions of low aH2O may prevent hornblendefrom being produced with peraluminous granitic liquids fromthe melting of biotite gneiss. Thus growth of hornblende inanatectic BPQ gneisses is an indication of addition of externalH2O-rich fluids during the partial melting event. KEY WORDS: biotite; dehydration; gneisses; hornblende; melt  相似文献   

    20.
    High‐pressure (HP) granulites and eclogitized metagabbro are exposed along an orogen‐parallel high‐P belt that was developed at c. 1050–1020 Ma in the NE Grenville Province. Among these rocks, mafic granulites derived from a Labradorian anorthosite suite of the Lelukuau terrane contain garnet, Al‐Na diopside, and, depending on bulk composition, plagioclase and kyanite. Moreover, the distribution of phases is influenced by the original igneous texture. For instance, in high XMgO leucocratic varieties, garnet porphyroblasts nucleated together with kyanite in An‐rich cores of plagioclase domains whereas in low XMgO rocks garnet occurs together with clinopyroxene within formerly igneous ferromagnesian domains and kyanite is missing. In contrast, garnet pseudomorphs after igneous plagioclase in melanocratic varieties display evidence of earlier corona development. Metamorphic textures are consistent with a two stage evolution: (a) development of garnet and Al‐Na‐diopside (Cpx1) under high‐P metamorphic conditions, concomitant with elimination of plagioclase in the mesocratic to melanocratic varieties; and (b) partial loss of Al‐Na from Cpx1 resulting in production of new andesitic plagioclase, and growth of new clinopyroxene (Cpx2) after garnet and quartz in leucocratic to mesocratic rocks consistent with decompression. Widespread equilibrium textures between garnet‐Pl2‐Cpx2 and/or reset Cpx1 are consistent with development at the thermal peak. Estimated P–T conditions for the presumed thermal peak fall in the range 1500–1800 MPa and 800–900 °C and are comparable to those recorded by eclogitized gabbros from other parts of the high‐P belt of the NE Grenville province. Low jadeite content of clinopyroxene from the HP granulites is attributed to the low bulk Na2O/(Na2O + CaO) of these rocks relative to common basaltic compositions. Scarcity of apparent retrograde textural overprint in both the HP granulites and the eclogites suggests fast subsequent cooling, consistent with extrusion of the high‐P belt towards the foreland shortly after the metamorphic peak.  相似文献   

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