共查询到20条相似文献，搜索用时 250 毫秒
1.
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
2.
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
3.
Reversals for the reaction 2 annite+3 quartz=2 sanidine+3 fayalite+2 H2O have been experimentally determined in cold-seal pressure vessels at pressures of 2, 3, 4 and 5?kbar, limiting annite +quartz stability towards higher temperatures. The equilibrium passes through the temperature intervals 500–540°?C (2?kbar), 550–570°?C (3?kbar), 570–590°?C (4?kbar) and 590–610°?C (5?kbar). Starting materials for most experiments were mixtures of synthetic annite +fayalite+sanidine+quartz and in some runs annite+quartz alone. Microprobe analyses of the reacted mixtures showed that the annites deviate slightly from their ideal Si/Al ratio (Si per formula unit ranges between 2.85 and 2.92, AlVI between 0.06 and 0.15). As determined by Mössbauer spectroscopy, the Fe3+ content of annite in the assemblage annite+fayalite +sanidine+quartz is around 5–7%. The experimental data were used to extract the thermodynamic standard state enthalpy and entropy of annite as follows: H 0 f,?Ann =?5125.896±8.319 [kJ/mol] and S 0 Ann=432.62±8.89 [J/mol/K] (consistent with the Holland and Powell 1990 data set), and H 0 f,Ann =?5130.971±7.939 [kJ/mol] and S 0 Ann=424.02±8.39 [J/mol/K] (consistent with the TWEEQ data base, Berman 1991). The preceeding values are close to the standard state properties derived from hydrogen sensor data of the redox reaction annite=sanidine+magnetite+H 2 (Dachs 1994). The experimental half-reversal of Eugster and Wones (1962) on the annite +quartz breakdown reaction could not be reproduced experimentally (formation of annite from sanidine+fayalite+quartz at 540°?C/1.035?kbar/magnetite-iron buffer) and probable reasons for this discrepancy remain unclear. The extracted thermodynamic standard state properties of annite were used to calculate annite and annite+quartz stabilities for pressures between 2 and 5?kbar. 相似文献
4.
Wilhelm Johannes 《Contributions to Mineralogy and Petrology》1984,86(3):264-273
The beginning of melting in the system Qz-Or-Ab-An-H2 O was experimentally reversed in the pressure range
kbar using starting materials made up of mixtures of quartz and synthetic feldspars. With increasing pressure the melting
temperature decreases from 690° C at 2 kbar to 630° C at 17 kbar in the An-free alkalifeldspar granite system Qz-Or-Ab-H2O. In the granite system Qz-Or-Ab-An-H2O the increase of the solidus temperature with increasing An-content is only very small. In comparison to the alkalifeldspar
granite system the solidus temperature increases by 3° C (7° C) if albite is replaced by plagioclase An 20 (An 40). The difference
between the solidus temperatures of the alkalifeldspar granite system and of quartz — anorthite — sanidine assemblages (system
Qz-Or-An-H2O) is approximately 50° C.
With increasing water pressures plagioclase and plagioclase-alkalifeldspar assemblages become unstable and are replaced by
zoisite+kyanite+quartz and zoisite+muscovite-paragonitess +quartz, respectively. The pressure stability limits of these assemblages are found to lie between 6 and 16 kbar at 600°
C. At high water pressures (10–18 kbar) zoisite — muscovite — quartz assemblages are stable up to 700 and 720° C. The solidus
curve of this assemblage is 10–20° C above the beginning of melting of sanidine — zoisite — muscovite — quartz mixtures.
The amount of water necessary to produce sufficient amounts of melt to change a metamorphic rock into a magmatic looking one
is only small. In case of layered migmatites it is shown that 1 % of water (or even less) is sufficient to transform portions
of a gneiss into (magmatic looking) leucosomes. High grade metamorphic rocks were probably relatively dry, and anatectic magmas
of granitic or granodioritic composition are usually not saturated with water. 相似文献
5.
Solidus temperatures have been determined for minimum melt compositions in the system Qz(SiO2)-Ab(NaAlSi3O8)-Or(KAlSi3O8) at P(fluid)=2,5 and 10 kbar and at various water activities. The dry solidus was investigated in a dry argon environment.
Water activities (aH2O) between 0.0 and 1.0 were obtained by using H2O-CO2 mixtures. The Or/Ab+Or ratio of first melts increases considerably with decreasing water activity. At 10 kbar it is 0.28
in the water-saturated system and 0.56 at water activity 0.1. The Qz-content does not change with changing water activities.
The Ab-content of minimum melts formed at high pressures and low aH2O may remain almost constant in ascending magmas that are cooling and crystallizing. Qz-content increases at the expense of
the Or-component. Solidus temperatures decrease considerably when aH2O increases slightly from zero. At 10 kbar, the temperature difference between dry melting and the solidus for aH2O=0.1 is 120°C. The influence of pure CO2 on the solidus is very limited in the investigated P-T range. The solidus is approximatively 760°C at aH2O=0.5 between 2 and 10 kbar and approximatively 830°C at aH2O=0.3. This means that melting of quartz-feldspar assemblages may induce dehydration reactions at P-T conditions of the granulite
facies. 相似文献
6.
Water-saturated and water-undersaturated experiments (a
H2
O = 1.0 and 0.5) were performed in the temperature range 780–1040°C at 2 and 5 kbar in order to determine the upper thermal
stability of phlogopite in granitic melts. Starting compositions were: (A) subaluminous mixtures of 20 wt % synthetic phlogopite
and 80 wt % synthetic anhydrous haplogranitic glass; (B) peraluminous mixtures (normative corundum = 4 %) of 20 wt % synthetic
phlogopite and 80 wt % synthetic anhydrous peraluminous haplogranitic glass. The molar quartz: albite: orthoclase ratio of
the glasses of the 2␣kbar runs was 35:39:26 and that of the 5 kbar runs 30:42:28. In the subaluminous system, phlogopite is
stable up to 820°C at a
H2
O = 1.0 and up to 780°C at a
H2
O = 0.5. At higher temperatures, it is replaced by enstatite. In the peraluminous system phlogopite has a remarkably higher
thermal stability (up to 1000°C at 5 kbar and a
H2
O = 1.0) and there is a temperature interval of 80°C at a
H2
O = 1.0, and 90–100°C at a
H2
O = 0.5 between the first appearance of enstatite and the disappearance of phlogopite. In the peraluminous system, phlogopite
is a solid solution (ss) of phlogopite, muscovite, talc and eastonite components. The crystalline product of the phlogopitess breakdown reaction is an aluminous enstatite. The MgO-content of the melt depends on the normative corundum content of the
starting material and the run temperature. It is independent of pressure. In the subaluminous system, the MgO-content ranges
between 0.05 and 0.3 wt % in the temperature interval 780–880°C at both investigated water activities. The MgO-content of
the peraluminous melts at a
H2
O = 1.0 ranges between 0.4 and 1.7 wt % and at a
H2
O = 0.5 between 0.2 and 1.4 wt % in the temperature range 780–980°C.
Received: 28 August 1995 / Accepted: 6 August 1996 相似文献
7.
Bjørn O. Mysen R. J. Arculus David H. Eggler 《Contributions to Mineralogy and Petrology》1975,53(4):227-239
Carbon dioxide solubilities in H2O-free hydrous silicate melts of natural andesite (CA), tholeiite (K 1921), and olivine nephelinite (OM1) compositions have been determined employing carbon-14 beta-track mapping techniques. The CO2 solubility increases with increasing pressure, temperature, and degree of silica-undersaturation of the silicate melt. At 1650° C, CO2 solubility in CA increases from 1.48±0.05 wt % at 15 kbar to 1.95±0.03 wt % at 30 kbar. The respective solubilities in OM1 are 3.41±0.08 wt % and 7.11±0.10 wt %. The CO2 solubility in K1921 is intermediate between those of CA and OM1 compositions. At lower temperatures, the CO2 contents of these silicate melts are lower, and the pressure dependence of the solubility is less pronounced. The presence of H2O also affects the CO2 solubility (20–30% more CO2 dissolves in hydrous than in H2O-free silicate melts); the solubility curves pass through an isothermal, isobaric maximum at an intermediate CO2/(CO2+H2O) composition of the volatile phase. Under conditions within the upper mantle where carbonate minerals are not stable and CO2 and H2O are present a vapor phase must exist. Because the solubility of CO2 in silicate melts is lower than that of H2O, volatiles must fractionate between the melt and vapor during partial melting of peridotite. Initial low-temperature melts will be more H2O-rich than later high-temperature melts, provided vapor is present during the melting. Published phase equilibrium data indicate that the compositional sequence of melts from peridotite +H2O+CO2 parent will be andesite-tholeiite-nephelinite with increasing temperature at a pressure of about 20 kbar. Examples of this sequence may be found in the Lesser Antilles and in the Indonesian Island Arcs. 相似文献
8.
In order to model the processes of formation of the highly alkaline (potassic) melts during the partial melting of the eclogite
nodules in kimberlites, experiments on the melting of the model and natural eclogites in presence of the H2O-CO2 and H2O-CO2-KCl fluids at 5 GPa and 1200 and 1300°C are performed. A comparative analysis of the phase relations in the systems with
H2O-CO2 and H2O-CO2-KCl demonstrate that KCl in the fluid equilibrated with eclogites intensifies their melting. It is related to both high Cl
concentration in the forming silicate melt (2.0–5.5 wt %) and its enrichment in K2O owing to the K-Na exchange reactions with the immiscible chloride melt. Because of these reactions, the K2O/Cl ratio in the melts increases with the KCl content in the system and reaches 2.5–3.5 in the silicate melts coexisting
with the immiscible chloride liquid. However, the ratio KCl/(H2O + CO2 + KCl) in the fluid does not influence on the ratio K2O/Cl in the melts. Thus, the solubility KCl in the melts, apparently, does not depend on presence of the H2O-CO2 fluid, at least, within the concentration range used in the experiments (up to 20 wt %). The experiments show that the deliberated
chloride liquid is necessary to form the potassium-rich chlorine-bearing silicate melts during the eclogite melting. It corresponds
to the KCl content in the system above 5 wt %. 相似文献
9.
Quartzo‐feldspathic veins emplaced within a migmatite terrane near Wilson Lake in the Grenville Province of central Labrador record a metamorphic event not evident in the host rocks. The discordant veins are undeformed and have undisturbed primary igneous/hydrothermal textures. Most of the veins contain euhedral kyanite, as well as aggregates of kyanite, K‐feldspar, phlogopite and minor dumortierite which are likely pseudomorphs after primary phengite. The reconstructed phengite compositions range from 3.1 to 3.2 Si per 11 oxygen formula unit. The pseudomorph assemblage is interpreted as the product of phengite + quartz melting under H2O‐undersaturated conditions, which brackets P–T conditions of formation to about 9–16 kbar and 775–875 °C. A parallel vein that is likely of the same generation contains the borosilicate phases, dumortierite, prismatine and grandidierite, but no kyanite. The borosilicate assemblages constrain the P–T conditions of vein crystallization to ≥10 kbar and c. 750–850 °C. Vein emplacement is constrained to T ≤ 875 °C at the same pressures, which is well within the kyanite zone. Because the host rocks and veins must have experienced the same P–T history following vein emplacement, the presence of unreacted sillimanite in the host migmatites implies insufficient time for host rock equilibration. Slow reaction rates because of anhydrous conditions are not a likely explanation given the abundance of biotite and hornblende in the host rocks. The ductility implied by the breakdown of a hydrous phase (phengite) and the production of an H2O‐undersaturated melt in the veins contrasts with the apparently brittle behaviour of the host rocks. The absence of deformation since the time of vein emplacement, even at temperatures above 750 °C, suggests that the deep crust in this part of Labrador had a very short residence time under conditions of the kyanite zone. Rapid decompression from those conditions is consistent with quartz + phengite melting and accounts for the relatively brittle behaviour of the terrane as it was uplifted. 相似文献
10.
The system KAlSiO4-Mg2SiO4-SiO2-H2O includes model representatives of (1) hydrous siliceous magma from subducted oceanic crust — the eutectic liquid in KAlSi3O8-SiO2-H2O, and (2) the overlying mantle peridotite — the assemblage forsterite+enstatite (Fo+En). In a series of partly schematic isobaric isothermal sections, the products of hybridization between the model materials at pressures between 20 and 30 kbar have been determined. The liquid dissolves peridotite components with little change in composition. Hybridization is not a simple mixing process, because of the incongruent melting of peridotitic assemblages with phlogopite (Ph). Hybridization causes solidification of the liquid, with products a sequence of three mineral assemblages: Ph, Ph+quartz (Qz), and Ph+En. The products represent an absolute geochemical separation and local concentration of all potassium from the liquid. Hybridization is accompanied by H2O-saturation of melts, and evolution of aqueous fluid. Although there are significant differences between the melt composition and that of the magma rising from subducted oceanic slab, and between Fo+En and the mantle rock, extrapolation of the results suggests that the conclusions can probably be extended to mantle conditions with sodium in the melt, and jadeitic clinopyroxene included in the hybrid products. 相似文献
11.
Oleg G. Safonov Elizaveta I. Kovaleva Svetlana A. Kosova H.M. Rajesh Georgy A. Belyanin Maria A. Golunova Dirk D. Van Reenen 《地学前缘(英文版)》2012,3(6):829-841
Reaction textures and fluid inclusions in the～2.0 Ga pyroxene-bearing dehydration zones within the Sand River biotite-hornblende orthogneisses（Central Zone of the Limpopo Complex） suggest that the formation of these zones is a result of close interplay between dehydration process along ductile shear zones triggered by H2O-CO2-salt fluids at 750—800℃and 5.5—6.2 kbar.partial melting,and later exsolution of residual brine and H2O-CO2 fluids during melt crystallization at 650—700℃.These processes caused local variations of water and alkali activity in the fluids,resulting in various mineral assemblages within the dehydration zone.The petrological observations are substantiated by experiments on the interaction of the Sand River gneiss with the H2O-CO-2-（K,Na）Cl fluids at 750 and 800℃and 5.5 kbar.It follows that the interaction of biotite-amphibole gneiss with H2O-CO2-（K.Na）Cl fluids is accompanied by partial melting at 750—800℃.Orthopyroxene-bearing assemblages are characteristic for temperature 800℃and are stable in equilibrium with fluids with low salt concentrations,while salt-rich fluids produce clinopyroxene-bearing assemblages.These observations arc in good agreement with the petrological data on the dehydration zones within the Sand River orthoeneisses. 相似文献
12.
Wilhelm Johannes 《Contributions to Mineralogy and Petrology》1980,74(1):29-34
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
13.
Mineralogical and geochemical data suggest that chloride components play an important role in the transformation and partial melting of upper mantle peridotites. The effect of KCl on the transformation of hydrous peridotite rich in Al2O3, CaO, and Na2O was examined in experiments aimed at studying interaction between model NCMAS peridotite with H2O-KCl fluid under a pressure of 1.9 GPa, temperatures of 900–1200°C, and various initial H2O/KCl ratios. The experimental results indicate that KCl depresses the solidus temperature of the hydrous peridotite: this temperature is <900°C at 1.9 GPa, which is more than 100°C lower than the solidus temperature (1000–1025°C) of hydrous peridotite in equilibrium with KCl-free fluid. The reason for the decrease in the melting temperature is that the interaction of KCl with silicates prevails over the effect of chloride on the water activity in the fluid. Experimental data highlight the key role of Al2O3 as a component controlling the whole interaction process between peridotite and H2O-KCl fluid. Garnet, spinel, and pargasite-edenite amphibole in association with aluminous orthopyroxene are unstable in the presence of H2O-KCl fluid at a chloride concentration in the fluid as low as approximately 2 wt % and are replaced by Cl-bearing phlogopite (0.4–1.1 wt % Cl). Interaction with H2O-KCl fluid does not, however, affect clinopyroxene and forsterite, which are the Al poorest phases of the system. Chlorine stabilizes phlogopite at relatively high temperatures in equilibrium with melt at temperatures much higher than the solidus (>1200°C). The compositional evolution of melt generated during the melting of model peridotite in the presence of H2O-KCl fluid is controlled, on the one hand, by the solubility of the H2O-KCl fluid in the melt and, on the other hand, by phlogopite stability above the solidus. At temperatures below 1050°C, at which phlogopite does not actively participate in melting reactions, fluid dissolution results in SiO2-undersaturated (35–40 wt %) and MgO-enriched (up to 45 wt %) melts containing up to 4–5 wt % K2O and 2–3 wt % Cl. At higher temperatures, active phlogopite dissolution and, perhaps, also the separation of immiscible aqueous chloride liquid give rise to melts containing >10 wt % K2O and 0.3–0.5 wt % Cl. Our experimental results corroborate literature data on the transformation of upper mantle peridotites into phlogopite-bearing associations and the formation of ultrapotassic and highly magnesian melts. 相似文献
14.
《地学前缘(英文版)》2022,13(4):101380
Melting experiments on ultramafic rocks rich in the hydrous minerals phlogopite or phlogopite + K-richterite, some including 5% of accessory phases, have been conducted at 15 and 50 kbar. The assemblages represent probable source components that contribute to melts in cratonic regions, but whose melt compositions are poorly known. A main series of starting compositions based on MARID xenoliths consisted of a third each of clinopyroxene (CPX), phlogopite (PHL) and K-richterite (KR) with or without 5% ilmenite, rutile or apatite. Additional experiments were run without KR and with higher proportions of accessory phases. Melt traps were used at near-solidus temperatures to facilitate accurate analysis of well-quenched melts, for which reversal experiments demonstrate equilibrium.Results show that KR melts rapidly and completely within 50 °C of the solidus, so that melts reflect the composition of the amphibole and its melting reaction. Melts have high SiO2 and especially K2O but low CaO and Al2O3 relative to basaltic melts produced from peridotites at similar pressures. They have no counterparts amongst natural rocks, but most closely resemble leucite lamproites at 15 kbar. KR and PHL melt incongruently to form olivine (OL) and CPX at 15 kbar, promoting SiO2 contents of the melt, whereas orthopyroxene OPX is increasingly stable at lower lithosphere pressures, leading to an increase in MgO and decrease in SiO2 in melts, which resemble olivine lamproites. Melts of mica pyroxenites without KR are richer in CaO and Al2O3 and do not resemble lamproites. These experiments show that low CaO and Al2O3 in igneous rocks is not necessarily a sign of a depleted peridotite source. Accessory phases produce melts exceptionally rich in P2O5 or TiO2 depending on the phases present and are unlike any melts seen at the Earth’s surface, but may be important agents of metasomatism seen in xenoliths. The addition of the 5% accessory phases ilmenite, rutile or apatite result in melting temperatures a few ten of degrees lower; at least two of these appear essential to explain the compositions of many alkaline igneous rocks on cratons.Melting temperatures for CPX + PHL + KR mixtures are close to cratonic geotherms at depths > 130 km: minor perturbations of the stable geotherm at >150 km will rapidly lead to 20% melting. Melts of hydrous pyroxenites with a variety of accessory phases will be common initial melts at depth, but will change if reaction with wall-rocks occurs, leading to volcanism that contains chemical components of peridotite even though the temperature in the source region remains well below the melting point of peridotite. At higher temperatures, extensive melting of peridotite will dilute the initial alkaline melts: this is recognizable as alkaline components in basalts and, in extreme cases, alkali picrites. Hydrous pyroxenites are, therefore, components of most mantle-derived igneous rocks: basaltic rocks should not be oversimplified as being purely melts of peridotite or of mixtures of peridotite and dry pyroxenite without hydrous phases. 相似文献
15.
The melting reaction: albite(solid)+ H2O(fluid) =albite-H2O(melt) has been determined in the presence of H2O–NaCl fluids at 5 and 9.2 kbar, and results compared with those obtained in presence of H2O–CO2 fluids. To a good approximation, albite melts congruently at 9 kbar, indicating that the melting temperature at constant
pressure is principally determined by water activity. At 5 kbar, the temperature (T)- mole fraction (X
(H2O) ) melting relations in the two systems are almost coincident. By contrast, H2O–NaCl mixing at 9 kbar is quite non-ideal; albite melts ∼70 °C higher in H2O–NaCl brines than in H2O–CO2 fluids for X
(H2O) =0.8 and ∼100 °C higher for X
(H2O) =0.5. The melting temperature of albite in H2O–NaCl fluids of X
(H2O)=0.8 is ∼100 °C higher than in pure water. The P–T curves for albite melting at constant H2O–NaCl show a temperature minimum at about 5 kbar. Water activities in H2O–NaCl fluids calculated from these results, from new experimental data on the dehydration of brucite in presence of H2O–NaCl fluid at 9 kbar, and from previously published experimental data, indicate a large decrease with increasing fluid pressure
at pressures up to 10 kbar. Aqueous brines with dissolved chloride salt contents comparable to those of real crustal fluids
provide a mechanism for reducing water activities, buffering and limiting crustal melting, and generating anhydrous mineral
assemblages during deep crustal metamorphism in the granulite facies and in subduction-related metamorphism. Low water activity
in high pressure-temperature metamorphic mineral assemblages is not necessarily a criterion of fluid absence or melting, but
may be due to the presence of low a
(H2O) brines.
Received: 17 March 1995/Accepted: 9 April 1996 相似文献
16.
Marian B. Holness 《Contributions to Mineralogy and Petrology》1995,118(4):356-364
An investigation was made of the effect of trace amounts of feldspar (Na and/or K) on dihedral angles in the quartz-H2O-CO2 system at 4 kbar and 450–1050°C. Quartz-quartz-H2O dihedral angles in feldspar-bearing quartz aggregates are observed to be the same as those in pure quartz aggregates at
temperatures below 500°C. Above this temperature, they decrease with increasing temperature until the solidus. The final angle
at the inception of melting is about 65° for microcline-quartz-H2O and microcline-albite-quartz-H2O, and much less than 60° (the critical value for formation of grain-edge fluid channels in an isotropic system) for the albite-quartz-H2O system. CO2 was observed to produce a constant quartz-quartz-fluid dihedral angle of 97° in feldspar-bearing quartz aggregates at all
temperatures studied. Also examined were the dihedral angles for the two co-existing supersolidus fluids in quartz aggregates.
In all systems the quartz-volatile fluid angle is greater than 60°, whereas the quartz-melt angle is lower than 60°. Both
super-solidus angles decrease with increasing temperature. The transition from nonconnected to connected poro- sity with increasing
temperature observed in the quartz-albite-H2O system some tens of degrees below the solidus (termed a permeability transition), if a common feature of rocks near their
melting points, will play an important role in controlling the permeability of high-grade rocks to aqueous fluids.
Received: 27 October 1993 / Accepted: 11 July 1994 相似文献
17.
Phase equilibria and melt productivity in the pelitic system: implications for the origin of peraluminous granitoids and aluminous granulites 总被引：26，自引：1，他引：25
Alberto E. Patiño Douce A. Dana Johnston 《Contributions to Mineralogy and Petrology》1991,107(2):202-218
Peraluminous granitoid magmas are a characteristic product of ultrametamorphism leading to anatexis of aluminous metasedimentary rocks in the continental crust. The mechanisms and characteristic length-scales over which these magmas can be mobilized depend strongly on their melt fraction, because of their high viscosities. Thus, it is of fundamental importance to understand the controls exerted by pressure, temperature and bulk composition of the source material on melt productivity. We have studied experimentally the vapour-absent melting behaviour of a natural metapelitic rock and our results differ greatly from those of previous experimental and theoretical investigations of melt productivity from metamorphic rocks. Under H2O-undersaturated conditions, bulk composition of the source material is the overriding factor controlling melt fraction at temperatures on the order of 850–900° C. Granitoid melts formed in this temperature interval by the peritectic dehydration-melting reaction: $$\begin{gathered} Biotite + plagioclase + aluminosilicate + quartz \hfill \\ = melt + garnet \hfill \\ \end{gathered} $$ have a restricted compositional range. As a consequence, melt fractions will be maximized from protoliths whose modes coincide with the stoichiometry of the melting reaction. This “optimum mode” (approximately 38% biotite, 32% quartz, 22% plagioclase and 8% aluminosilicate) reflects the fact that generation of low-temperature granitoid liquids requires both fusible quartzo-feldspathic components and H2O (from hydrous minerals). Metapelitic rocks rich in mica and aluminosilicate and poor in plagioclase contain an excess of refractory material (Al2O3, FeO, MgO) with low solubility in low-temperature silicic melts, and will therefore be poor magma sources. Melt fraction varies inversely with pressure in the range 7–13 kbar, but the effect is not strong: the decrease (at constant temperature) over this pressure range is of at most 15 vol% (absolute). The liquids produced in our experiments are silicarich (68–73 wt% SiO2), strongly peraluminous (2–5 wt% normative corundum) and very felsic (MgO+FeO* +TiO2 less than 3 wt%, even at temperatures above 1000° C). The last observation suggests that peraluminous granitoids with more than 10% mafic minerals (biotite, cordierite, garnet) contain some entrained restite. Furthermore, because liquids are also remarkably constant in composition, we believe that restite separation is more important than fractional crystallization in controlling the variability within and among peraluminous granitoids. We present liquidus phase diagrams that allow us to follow the phase relationships of melting of silica-and alumina-saturated rocks at pressures corresponding to the mid- to deep-continental crust. Garnet, aluminosilicate, quartz and ilmenite are the predominant restitic phases at temperatures of about 900° C, but Ti-rich biotite or calcic plagioclase can also be present, depending on the bulk composition of the protolith. At temperatures above 950–1050° C (depending on the pressure) the restitic assemblage is: hercynitic spinel+ilmenite+quartz±aluminosilicate. Our results therefore support the concept that aluminous granulites (garnet-spinel-plagioclase-aluminosilicate-quartz) can be the refractory residuum of anatectic events. 相似文献
18.
Takanobu OBA 《Journal of Earth System Science》1990,99(1):81-90
The join tremolite (Tr)-pargasite (Pa) was studied at temperatures between 800 and 1150°C under water vapour pressure of 10 kbar. The results show a continuous solid solution of amphibole between the composition Tr80Pa20 and Pa100 at 800°C and 10kb. Pargasite melts incongruently and breaks down at high temperature to clinopyroxene+forsterite+spinel+L+V. A single phase amphibole with composition lying between Tr80Pa20 and nearly pure Pa, breaks down to amphibole of different composition plus other phases. The stability fields of amphibole spread toward higher temperature side with increasing pargasite content, and pargasite itself has the widest stability field. At subliquidus, the composition of amphibole coexisting with other phases becomes more pargasitic with increasing temperature. The compositions of liquid, which are formed by partial melting of amphibole of Tr40Pa60 composition (Fo-normative) under water vapour pressure of 10 kbar, are alumina-rich and Qz-normative. 相似文献
19.
Reactions and partial melting of peraluminous rocks in the presence of H2O-CO2–salt fluids under parameters of granulite-facies metamorphism were modeled in experiments on interaction between orthopyroxene–cordierite–biotite–plagioclase–quartz metapelite with H2O, H2O-CO2, H2O-CO2-NaCl, and H2O-CO2-KCl fluids at 600 MPa and 850°C. Rock melting in the presence of H2O and equimolar H2O-CO2 fluids generates peraluminous (A/CNK1 > 1.1) melts whose composition corresponds to magnesian calcic or calc–alkaline S-type granitoids. The melts are associated with peritectic phases: magnesian spinel and orthopyroxene containing up to 9 wt % Al2O3. In the presence of H2O-CO2-NaCl fluid, cordierite and orthopyroxene are replaced by the association of K-Na biotite, Na-bearing gedrite, spinel, and albite. The Na2O concentrations in the biotite and gedrite are functions of the NaCl concentrations in the starting fluid. Fluids of the composition H2O-CO2-KCl induce cordierite replacement by biotite with corundum and spinel and by these phases in association with potassium feldspar at X KCl = 0.02 in the fluid. When replaced by these phases, cordierite is excluded from the melting reactions, and the overall melting of the metapelite is controlled by peritectic reactions of biotite and orthopyroxene with plagioclase and quartz. These reactions produce such minerals atypical of metapelites as Ca-Na amphibole and clinopyroxene. The compositions of melts derived in the presence of salt-bearing fluids are shifted toward the region with A/CNK < 1.1, as is typical of so-called peraluminous granites of type I. An increase in the concentrations of salts in the fluids leads to depletion of the melts in Al2O3 and CaO and enrichment in alkalis. These relations suggest that the protoliths of I-type peraluminous granites might have been metapelites that were melted when interacting with H2O-CO2-salt fluids. The compositions of the melts can evolve from those with A/CNK > 1.1 (typical of S-type granites) toward those with A/CNK = 1.0–1.1 in response to an increase in the concentrations of alkali salts in the fluids within a few mole percent. Our experiments demonstrate that the origin of new mineral assemblages in metapelite in equilibrium with H2O-CO2-salt fluids is controlled by the activities of alkaline components, while the H2O and CO2 activities play subordinate roles. This conclusion is consistent with the results obtained by simulating metapelite mineral assemblages by Gibbs free energy minimization (using the PERPE_X software), as shown in log(\({a_{{H_2}O}}\))–log(\({a_{N{a_2}O}}\)) and log(\({a_{{H_2}O}}\))–log(\({a_{{K_2}O}}\)) diagrams. 相似文献
20.
Hydrothermal experiments with H2O-CO2 fluids at Pfluid = 6 kbar yielded the following quilibrium conditions for reactions important in metamorphosed siliceous dolomites (T = °C; X = Xco2): (3) dolomite + 2 quartz = diopside + 2 CO2T = 620 ± 8X = 0.73 ± 0.03 (5) 5 dolomite + 8 quartz + H2O = tremolite + 3 calcite + 7 CO2T = 600 ± 5 550 ±5 540±5 500±5X = 0.66 ± 0.03 0.21 ± 0.03 0.21 ± 0.04 0.06 ± 0.02 (7) 3 dolomite + 4 quartz + H2O = talc + 3 calcite + 3 CO2T = 550±5 500±5 450 ±5X = 0.25 ± 0.05 0.07 ± 0.02 0.03 ± 0.02 (8) 2 dolomite + talc + 4 quartz = tremolite + 4 CO2T = 550 ± 5 540 ±5 500 ± 5X = 0.22 ± 0.03 0.21 ± 0.02 0.06 ± 0.02 A thermodynamically self-consistent 6 kbar T-XCO2, topology results by extrapolating equilibria from experimental brackets using a modified Redlich-Kwong equation for activities in H2O-CO2 mixtures. This topology restricts the assemblage talc + calcite to a narrow stability band in T-XCO2 space at XCO2 < 0.55 and T < 590°C. Accordingly, the occurrence of talc + calcite in pure siliceous dolomites metamorphosed at Pfluid = 6 kbar implies correspondingly water-rich fluids. 相似文献