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1.
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   

2.
A cylinder of amphibolite comprising the assemblage amphibole+clinozoisite+albite has been frictionally melted using radial friction welding apparatus. This was achieved by rotating a steel ring at 750 rpm and a force of 98 kN for 10 s against a stationary steel casing which housed the rock sample. The ring penetrated the casing then proceeded to rotate and compress the sample to 95% of its original volume until it cracked at right angles to its length. This generated a whole rock silicate melt which injected the crack and on cooling produced glass, crystallites and vesicles. Melting occurred in two stages: an initial low pressure melting event with crystallization to augite+Fe-rich anorthite, followed by a high pressure melting event with crystallization to fassaitic clinopyroxene. It is estimated that pressures of 0.5 GPa rising to 1 GPa were realized at the ring-rock interface. Under these conditions fassaite superseded augite+anorthite crystallization due to the increased solubility of Ca-Tschermak's component in clinopyroxene. The high pressure event provides a crude analogue for the frictional melting of basic rock at depths of 15–30 km in a seismogenic fault: a situation realized along the slip zone between cold descending lithosphere and overlying mantle during subduction.  相似文献   

3.
Eclogites characterized by a garnet + clinopyroxene + orthopyroxene + sanidine + rutile assemblage are reported for the first time in the eastern Bangong suture, central Tibet (China). Garnet and sanidine are exsolved from clinopyroxene. Al‐exchange barometer for orthopyroxene and garnet and K concentrations in clinopyroxene indicate a peak pressure of ～4 GPa. The occurrence of these ultrahigh‐pressure rocks implies the subduction of continental crust to a depth of >130 km along the eastern Bangong suture zone during the Early Jurassic. The denudation of these ultrahigh‐pressure metamorphic rocks could have provided a significant source for the Jurassic turbidites in the western Bangong ocean basin.  相似文献   

4.
Suprasolidus phase relations at pressures from 8 to 30 kb andtemperatures from 950 to 1380C have been determined experimentallyfor a glassy armalcolite–phlogopite lamproite from thechilled margin of a medium–grained lamproite from SmokyButte, Montana: The armalcolite-phlogopite lamproite has microphenocrystsof olivine in a groundmass of phlogopite, sanidine, armalcolite,clinopyroxene, chromite, priderite, apatite, and abundant glass.The lamproite is SiO2-rich and has high F/H2O relative to lamproitesthat have been investigated in previous experimental studies.Our data show that with decreasing temperature from the liquidusat pressures above 12 kb, melt coexists successively with:olivine; orthopyroxene + clinopyroxene; orthopyroxene + clinopyroxene+ phlogopite; clinopyroxene +phlogopite; and clinopyroxene +orthopyroxene + K-richterite. Below 12 kb, the assemblage successionis: olivine; olivine + clinopyroxene; olivine + clinopyroxene+ phlogopite; and olivine +clinopyroxene + phlogopite + armalcolite.The main difference from the natural paragenesis is that therock does not contain any orthopyroxene—a feature thatis rather remarkable inasmuch as it has 16% normative hypersthene—andthe rock differs also in that it contains sanidine and priderite.In the experiments, sanidine is observed only as ghostlike domainsin some of the glass and appears to have formed during quenching. The solid phases crystallized experimentally are generally compositionallysimilar to the minerals in the rock. These similarities andthe experimental phase relations support the concept of a rapidinitial magma ascent with only a small temperature drop andcrystallization of olivine, but not of orthopyroxene. At lowerpressures, less than 12 kb, it appears that the magma ascendedmore slowly with a larger temperature drop suggested by thesimilarity of the experimentally determined sequence of assemblagesto the paragenesis of the rock. No quasi-invariant multiphase-saturation point was found suchas might be indicative of pressure and temperature conditionsfor formation of the lamproite magma by eutectic-type partialmelting of a mantle source. The occurrence of olivine, orthopyroxene,and clinopyroxene near the liquidus, and the high proportionof normative hypersthene in the melt suggest that lherzoliteor harzburgite was probable in the magma source rock. The highSiO2 and MgO contents of the Smoky Butte lamproites may indicatethat orthopyroxene was a source mineral even though it did notcrystallize under near-surface conditions. The curve definingthe appearance of phlogopite appears at progressively lowertemperatures from the liquidus as pressure increases, so itwould appear that either phlogopite was not the mantle K-reservoir,or it was entirely consumed during the partial melting process.The composition of the near-liquidus glass in the experimentsis likely to be the composition of the bulk rock less the verysmall amounts of olivine + clinopyroxene + orthopyroxene crystallizedwithin a few degrees below the liquidus. From the inferred compositionof this glass, anhydrous phlogopite is a potential mineral.The principal variable that determines whether phlogopite crystallizesas a near-liquidus mineral is F/H2O; low values of this ratiopromote the presence of phlogopite as a near-liquidus mineralwhereas high values deter its crystallization. The common practiceof adding H2O but not F in experiments to compensate for degassingmay obscure the role of phlogopite in the evolution of lamproitemagmas.  相似文献   

5.
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   

6.
The paper presents materials on the fabric of the western, southwestern, and southern exocontact zones of the Khibina alkaline pluton and metavolcanic rocks of the Il’mozerskaya Formation of the Paleoproterozoic Imandra-Varzuga riftogenic structure. The volcanics of the Imandra-Varzuga structure were originally metamorphosed to the greenschist facies (at temperatures of ≥300°C and pressures of ≥2.0–2.5 kbar) and were afterward metamorphosed to the pyroxene-hornfels facies under the thermal effect the Khibina pluton with the development of a hornfels zone 150–400 m thick. According to their composition, the hornfelses are subdivided into three zones: inner, intermediate, and outer. The inner zone is up to 30 m thick and consists of hornfelses of clinopyroxene-plagioclase composition with olivine as a typomorphic mineral and with variable amounts of amphibole. The intermediate zone occurs at a distance of 30–200 m from the pluton, is separated from the inner zone by the olivine isograde, and consists of amphibole-clinopyroxene-plagioclase hornfelses. The outer zone, 200–400 m away from the contact of the pluton, is made of fine-grained melanocratic hornblende hornfelses. The thermal transformations of the metavolcanics involved the gradual replacement of their low-temperature mineral assemblage (actinolite + albite) by a higher temperature one (clinopyroxene + amphibole + andesinebytownite ± olivine). Our data on the chemical composition of the rock-forming minerals of the hornfelses indicate that the olivine is ferrohortonolite-fayalite, the clinopyroxene belongs to the augite-ferroaugite series, and occasional orthopyroxene grains (which were found only in the intermediate zone) are ferrohypersthene. The amphibole in the hornfelses of the intermediate zone and the outermost (farthest from the contact) part of the inner zone is edenite, a Ca amphibole. The amphibole in hornfelses near the contact is kataphorite of the Na-Ca amphibole group. The plagioclase composition generally corresponds to andesine and bytownite and is albite-oligoclase near the contact with the pluton. The hornfelses adjacent to the contact bear rare sanidine grains. The mineral thermo-and barometry of the hornfelses yielded temperatures of 700–640°C and pressures of 1–1.5 kbar. The temperature determined for the zone exactly at the contact was approximately 700°C, which corresponds to the initial temperature of the rocks in contact with the magma and is close to the crystallization temperature of the nepheline syenites of the Khibina pluton.  相似文献   

7.
The temperatures and pressures of subsolidus equilibration of garnet-websterites (garnet+clinopyroxene+orthopyroxene) can be determined to within 3 kilobars from alumina solubility properties of clinopyroxene (Herzberg, 1978) and orthopyroxene (Wood, 1974, 1975). These calculations require knowledge of the oxidation state of iron and the effect of alumina on the mutual solubility of the two pyroxenes. The conditions of total dissolution of exsolved garnet and orthopyroxene required to yield single-phase subcalcic clinopyroxenites from Salt Lake Crater and the French Pyrenees have been determined. Many of these clinopyroxenites were transported 20 to 60 km up the mantle column before exsolution was terminated. Such transport was probably accomplished by convective upwelling of hot mantle peridotite and its contained anatectic products, rather than by precipitation from ascending magmas.  相似文献   

8.
Pyroxenite xenoliths are relatively common in an alkali trachybasalt in the Glen Innes area in northeastern New South Wales where they coexist with peridotite xenoliths, probably lherzolitic. The pyroxenites vary widely in modal composition. Several pyroxenite xenoliths are characterised by megacrystals of subcalcic clinopyroxene and enstatite, the former comprising a unique group of high pressure pyroxenes in which exsolution of orthopyroxene has proceeded on a megascopic scale. Garnet is absent from all mineral assemblages. Mineralogical and experimental data suggest that the subcalcic clinopyroxene and orthopyroxene megacrystals equilibrated initially at temperatures and pressures of the order of 1350–1450° C and 10–23 kb respectively. The most common xenoliths, namely diopsideorthopyroxene assemblages in which there is evidence of subsolidus annealing, equilibrated at comparable pressures but a significantly lower temperatures (ca. 1000° C). It is suggested that the pyroxenites and associated peridotite xenoliths are samples of essentially unmodified layered upper mantle.  相似文献   

9.
In the system CaO-MgO-Al2O3-SiO2, the tetrahedron CaMgSi2O6(di)-Mg2SiO4(fo)-SiO2-CaAl2 SiO6(CaTs) forms a simplified basalt tetrahedron, and within this tetrahedron, the plane di-fo-CaAl2Si2O8(an) separates simplified tholeiitic from alkalic basalts. Liquidus phase relations on this join have been studied at 1 atm and at 7, 10, 15, and 20 kbar. The temperature maximum on the 1 atm isobaric quaternary univariant line along which forsterite, diopside, anorthite, and liquid are in equilibrium lies to the SiO2-rich side of the join di-fo-an. The isobaric quaternary invariant point at which forsterite, diopside, anorthite, spinel, and liquid are in equilibrium passes, with increasing pressure, from the silica-poor to the silica-rich side of the join di-fo-an, which causes the piercing points on this join to change from forsterite+diopside+anorthite+liquid and forsterite +spinel+anorthite+liquid below 5 kbar to forsterite +diopside+spinel+liquid and diopside +spinel+anorthite+liquid above 5 kbar. As pressure increases, the forsterite and anorthite fields contract and the diopside and corundum fields expand. The anorthite primary phase field disappears entirely from the join di-fo-an between 15 and 20 kbar. Below about 4 kbar, the join di-fo-an represents, in simplified form, a thermal divide between alkalic and tholeiitic basalts. From about 4 to at least 12 kbar, alkalic basalts can produce tholeiitic basalts by fractional crystallization, and at pressures above about 12 kbar, it is possible for alkalic basalt to be produced from oceanite by crystallization of both olivine and orthopyroxene. If alkalic basalts are primary melts from a lherzolite mantle, they must be produced at high pressures, probably greater than about 12 kbar.Department of Geosciences, University of Texas at Dallas Contribution No. 327. Hawaii Institute of Geophysics Contribution No. 814.  相似文献   

10.
Anhydrous partial melting experiments, at 10 to 30 kbar from solidus to near liquidus temperature, have been performed on an iron-rich martian mantle composition, DW. The DW subsolidus assemblage from 5 kbar to at least 24 kbar is a spinel lherzolite. At 25 kbar garnet is stable at the solidus along with spinel. The clinopyroxene stable on the DW solidus at and above 10 kbar is a pigeonitic clinopyroxene. Pigeonitic clinopyroxene is the first phase to melt out of the spinel lherzolite assemblage at less than 20°C above the solidus. Spinel melts out of the assemblage about 50°C above the solidus followed by a 150° to 200°C temperature interval where melts are in equilibrium with orthopyroxene and olivine. The temperature interval over which pigeonitic clinopyroxene melts out of an iron-rich spinel lherzolite assemblage is smaller than the temperature interval over which augite melts out of an iron-poor spinel lherzolite assemblage. The dominant solidus assemblage in the source regions of the Tharsis plateau, and for a large percentage of the martian mantle, is a spinel lherzolite.  相似文献   

11.
Summary Supra-solidus phase relations at temperatures and pressures ranging from 800 to 1700 °C and 2 to 6.4 GPa have been determined experimentally for three silica-rich lamproites: hyalo-leucite phlogopite lamproite (Oscar, West Kimberley); sanidine richterite lamproite (Cancarix, Murcia-Almeria); and phlogopite transitional madupitic lamproite (Middle Table Mountain, Wyoming). All samples have extended melting intervals (500–600 °C). Bulk composition has a significant control on the nature of the initial liquidus phases, with orthopyroxene occurring at low pressures (<4 GPa) in the relatively calcium-poor Oscar and Cancarix lamproites. At higher pressure (>6 GPa) orthopyroxene is replaced by garnet plus clinopyroxene as near-liquidus phases in the Oscar lamproite and by orthopyroxene plus clinopyroxene in the Cancarix sample. Clinopyroxene is a near-liquidus phase at all pressures in the Middle Table Mountain lamproite. Near-solidus phase assemblages at high pressure (>5 GPa) are: clinopyroxene + phlogopite + coesite + rutile + garnet (Oscar); clinopyroxene + garnet + coesite + K–Ti-silicate (Cancarix); clinopyroxene + phlogopite + apatite + K–Ti-silicate (Middle Table Mountain). In all compositions olivine is never found as a liquidus phase at any of the temperatures or pressures studied here. The phase relationships are interpreted to suggest that silica-rich lamproites cannot be derived by the partial melting of lherzolitic sources. Their genesis is considered to involve high degrees of partial melting of ancient metasomatic veins within a harzburgitic-lherzolitic lithospheric substrate mantle. The veins are considered in their mineralogy to be similar to the experimentally-observed, high pressure, near-solidus phase assemblages. The composition of silica-rich primary lamproite magmas differs between cratons as a consequence of differing mineralogical modes of the source veins and different relative contributions from the veins and wall-rocks to the partial melts. Received February 21, 2000; revised version accepted July 3, 2001  相似文献   

12.
The metamorphic evolution of a granulitized eclogite from the Phung Chu Valley (Eastern Himalaya) was reconstructed combining microstructural observations, conventional thermobarometry and quantitative pseudosection analysis. The granulitized eclogite consists of clinopyroxene, plagioclase, garnet, brown amphibole, and minor orthopyroxene, biotite, ilmenite and quartz. On the basis of microstructural observations and mineral relationships, four metamorphic stages and related mineral assemblages have been recognized: (i) M1 eclogite‐facies assemblage, consisting of garnet, omphacite (now replaced by a clinopyroxene + plagioclase symplectite) and phengite (replaced by biotite +plagioclase symplectite); (ii) M2 granulite‐facies assemblage, represented by clinopyroxene, orthopyroxene, garnet, plagioclase and accessory ilmenite; (iii) M3 plagioclase + orthopyroxene corona developed around garnet, and (iv) M4 brown amphibole + plagioclase assemblage in the rock matrix. Because of the nearly complete lack of eclogitic mineral relics, M1 conditions can be only loosely constrained at >1.5 GPa and >580 °C. In contrast, assemblage M2 tightly constrains the peak granulitic stage at 0.8–1.0 GPa and >750 °C. The second granulitic assemblage M3, represented by the plagioclase + orthopyroxene corona, formed at lower pressures (～0.4 GPa and ～750 °C). During the subsequent exhumation, the granulitized eclogite experienced significant cooling to nearly 700 °C, marked by the appearance of brown amphibole and plagioclase (M4) in the rock matrix. U‐Pb SHRIMP analyses on low‐U rims of zircon from an eclogite of the same locality suggest an age of 13–14 Ma for the M3 stage. The resulting decompressional clockwise P–T path of the Ama Drime eclogite is characterized by nearly isothermal decompression from >1.5 GPa to ～0.4 GPa, followed by nearly isobaric cooling from ～775 °C to ～710 °C. Modelling of phase equilibria by a calculated petrogenetic grid and conventional thermobarometry on a biotite‐garnet‐sillimanite metapelite hosted in the country rock granitic orthogneiss extends the inferred P–T trajectory down to ～630 °C and ～0.3 GPa.  相似文献   

13.
The Cayconi district of the Cordillera de Carabaya, SE Peru, exposes a remnant of an upper Oligocene–Lower Miocene (22.2–24.4 Ma) volcanic field, comprising a diverse assemblage of S-type silicic and calc-alkaline basaltic to andesitic flows, members of the Picotani Group of the Central Andean Inner Arc. Basaltic flows containing olivine, plagioclase, clinopyroxene, ilmenite and glass, and glassy rhyolitic agglutinates with phenocrystic quartz, cordierite, plagioclase, sanidine, ilmenite and apatite, respectively exhibit mineralogical and geochemical features characteristic of medium-K mafic and Lachlan S-type silicic lavas. Cordierite-bearing dacitic agglomerates and lavas, however, are characterized by dispersed, melanocratic micro-enclaves and phenocrysts set in a fine-grained quartzo-feldspathic matrix. They contain a bimodal mica population, comprising phlogopite and biotite, as well as complexly zoned, sieve-textured plagioclase grains, sector-zoned cordierite, sanidine, quartz, irregular patches of replaced olivine, clinopyroxene and orthopyroxene and accessory phases including zircon, monazite, ilmenite and chromite. The coexistence of minerals not in mutual equilibrium and the growth/dissolution textures exhibited by plagioclase are features indicative of magmatic commingling and mixing. Trachytic-textured andesite flows interlayered with olivine+plagioclase–glomerophyric, calc-alkaline basalts have a phenocrystic assemblage of resorbed orthopyroxene and plagioclase and exhibit melanocratic groundmass patches of microphenocrystic phlogopite, Ca-rich sanidine, ilmenite and aluminous spinel. The mineralogical and mineral chemical relationships in both the dacites and the trachytic-textured andesites imply subvolcanic mixing between distinct ultrapotassic mafic melts, not represented by exposed rock types, and both the S-type silicic and calc-alkaline mafic magmas. Such mixing relationships are commonly observed in the Oligo-Miocene rocks of the Cordillera de Carabaya, suggesting that the S-type rocks in this area and, by extension, elsewhere derive their unusually high K2O, Ba, Sr, Cr and Ni concentrations from commingling and mixing with diverse, mantle-derived potassic mafic magmas.  相似文献   

14.
Evidence is presented for the primary high pressure crystallization of the Ewarara, Kalka and Gosse Pile layered intrusions which form part of the Giles Complex in central Australia. These pressures are estimated at 10 to 12 kb. The high pressure characteristics include subsolidus reactions between olivine and plagioclase, orthopyroxene and plagioclase, and orthopyroxene and spinel; spinel and rutile exsolution in both ortho- and clino-pyroxene; spinel exsolution in plagioclase; high Al2O3 and Cr2O3 contents of both ortho- and clinopyroxene; high AlVI in clinopyroxene; dominance of orthopyroxene as an early crystallizing phase; high distribution coefficients for co-existing pyroxene pairs; and thin chilled margins. Such phenomena are rare in documented layered basic intrusions.  相似文献   

15.
The crystallization sequences in olivine-rich nephelinitic andbasanitic compositions have been experimentally studied underdry conditions at pressures up to 36 kb. Electron microprobeanalyses of olivines, clinopyroxenes, garnets, and orthopyroxenesenable calculation of possible crystal fractionation trendsfor these magmas at various pressures. Low-pressure fractionationis dominated by olivine and yields derivative liquids of highersilica content and showing rapid iron enrichment. At pressuresof 18–27 kb, fractionation is controlled by aluminousclinopyroxene with minor olivine or garnet. Derivative liquidsshow marked depletion in calcium accompanying silica depletionand increasing degree of undersaturation. .At pressures greaterthan 27 kb, crystal fractionation is controlled by garnet+clinopyroxeneseparation. Chemical analyses of these phases allow quantitativecalculations of possible fractionation which show that largedegrees of crystallization are required to produce quite smallchanges in silica content and in degree of undersaturation.In addition, fractionation by garnet and clinopyroxene separationis accompanied by depletion in calcium content in the more undersaturatedrocks and high degrees of crystallization are necessarily accompaniedby enrichment in iron relative to magnesium. These effects areinconsistent with the characteristics of natural magmas of mantlederivation in the range from alkali olivine basalts to olivinemelilitites. It is concluded that separation of garnet and clinopyroxeneunder upper mantle conditions does not produce the natural magmaseries from olivine-rich tholeiite to olivine nephelinite andolivine melilitite. The transient role of orthopyroxene overa very small P, T range in the melting interval of two of theexperimental compositions suggests that an olivine-rich basanitemay be developed by small degrees of partial melting of a sourcepyrolite under dry conditions at 60–80 km depth. Thisliquid, which would form in equilibrium with residual olivine,aluminous orthopyroxene, and aluminous clinopyroxene, wouldcontain approximately 5 per cent normative orthoclase, 5 percent albite, 12 per cent nepheline, 20 per cent anorthite, 22per cent diopside, and 31 per cent olivine.  相似文献   

16.
A regional study of olivine-bearing metagabbros in the Adirondacks has permitted testing of the P(pressure)-T(temperature)-X(composition) dependence of garnet-forming reactions as well as providing additional regional metamorphic pressure data. Six phases, olivine, orthopyroxene, clinopyroxene, garnet, plagioclase and spinel, which can be related by the reactions: orthopyroxene+clinopyroxene+spinel +anorthite=garnet, and forsterite+anorthite=garnet occur together both in coronal and in equant textures indicative of equilibrium. Compositions of the respective minerals are typically Fo25–72, En44–75, En30–44Fs9–23Wo47–49, Pp13–42Alm39–63Gr16–20, An29–49 and Sp16–58. When they occur in the same rock, equant and coronal garnets are homogeneous and compositionally identical suggesting that chemical equilibrium may have been attained despite coronal textures. Extrapolating reactions in the simple CMAS system to granulite temperatures and making thermodynamic corrections for solid solutions gives equilibration pressures (using the thermometry of Bohlen et al. 1980b) ranging from about 6.5 kb in the Lowlands and southern Adirondacks to 7.0–8.0 kb in the Highlands for the assemblage olivine-plagioclase-garnet. These results are consistent with inferred peak metamorphic conditions in the Adirondacks (Valley and Bohlen 1979; Bohlen and Boettcher 1981). Thus the isobaric retrograde path suggested by Whitney and McLelland (1973) and Whitney (1978) for the formation of coronal garnet in olivine metagabbros may not be required. Application of the same equilibria gives >8.7 kb for South Harris, Scotland and 0.9 kb for the Nain Complex. Disagreement of the latter value with orthopyroxeneolivine-quartz barometry (Bohlen and Boettcher 1981) suggests that the use of iron-rich rocks (olivines Fa50) results in errors in calculated pressures.Contribution No. 385 from the Mineralogical Laboratory, Department of Geological Sciences, The University of Michigan, Ann Arbor, Michigan 48109, USA  相似文献   

17.
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   

18.
Essentially two types of ultramafic inclusions occur in the basanitic lavas and ejecta deposits of the northwestern Grand Canyon, Arizona. Abundant, olivine-rich nodules contain an emerald green, chrome-rich diopside and chrome-rich spinels. A much less common group of inclusions generally containing poikilitic kaersutite have more variable modal compositions, more variable but iron-rich and chrome-poor mineral compositions, and are characterized by the presence of a titaniferous clinopyroxene which appears black in hand specimen. The nature and petrologic significance of these black clinopyroxene-bearing inclusions, together with megacrysts of kaersutite and black clinopyroxene, are discussed in this paper.Petrographic aspects indicate an origin as cumulates of fractionating basaltic magma. Compositions of pyroxenes suggest high pressures of crystallization. The co-precipitation of orthopyroxene, clinopyroxene, olivine and Mg-spinel from what in all probability was under-saturated magma, together with the total absence of feldspar as a cumulate or intercumulate phase, is compatible with crystallization near 10 kb, on the basis of quite limited experimental data on anhydrous basaltic compositions. Pressures of this sort are attained at depths close to the mantle-crust boundary in the western Grand Canyon. By way of comparison, cumulate-textured inclusions from central Nevada containing rare orthopyroxene, widespread plagioclase, and more Fe-enriched clinopyroxenes, kaersutites, olivines and spinels are postulated to have crystallized at lower temperatures (or at a more advanced stage of fractionation) and possibly at lower pressures.Numerous occurrences, worldwide, of kaersutite-bearing inclusions, always in undersaturated host rocks, have recently been reported. Compositionally, the kaersutites are quite uniform, whether coexistent with pyropic garnet-clinopyroxene (Kakanui, New Zealand), with ortho-pyroxene-clinopyroxene-olivine-Mg spinel (Grand Canyon), or with plagioclase-clinopyroxene-olivine-magnetite. The last assemblage is found in shallow-seated igneous bodies of alkalic, mafic composition, as well as in inclusions within basaltic rocks. These occurrences imply the precipitation of kaersutite amphibole over a broad range of pressures, and as high as those prevailing in the upper mantle.  相似文献   

19.
Melting experiments involving fifteen runs were performed at pressures between 1.0 and 2.0 GPa in order to locate the liquidus temperatures, the solidus temperatures, and the melting intervals of the Wannienta basaltic magma, northern Taiwan. The experimental results showed that the liquidus and solidus temperatures were raised by 60 GPa and 40 GPa respectively. The liquidus mineral at 1.0 GPa is orthopyroxene, whereas the liquidus mineral is clinopyroxene at 1.5 and 2.0 GPa. The crystallized phases are clinopyroxene and plagioclase at temperatures between 1220 and 1270°C and pressures between 1.0 and 2.0 GPa. Garnet appears at 2.0 GPa near the solidus. The geochemical evolution of the residual magma with decreasing temperature show the following trends: At 1.0 GPa, Al, Na, and K are progressively enriched while depletions occur in Mg. At 2.0 GPa, Si, Fe and K are progressively enriched with decreasing temperature while depletions occur in Mg, Ca, and Na. The fractionation trend of the Kuanyinshan volcanic series is similar to the trend observed in residual magmas at pressures between one atmosphere and 1.0 GPa. These results indicate that the depth for fractional crystallization of the Wannienta basaltic magma to produce andesites could be modeled at low pressure. The fractionates involved included iron-titanium oxides, olivine, plagioclase, and clinopyroxene.  相似文献   

20.
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   

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