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1.
We have conducted high pressure (to 3 kbar), water saturated melting experiments on an andesite (62 wt% SiO2) and a basaltic andesite (55 wt% SiO2) from western Mexico. A close comparison between the experimental phase assemblages and their compositions, and the phenocryst
assemblages of the lavas, is found in water saturated liquids, suggesting that the CO2 content was minimal in the fluid phase. Thus the historic lavas from Volcan Colima (with phenocrysts of orthopyroxene, augite,
plagioclase, and hornblende) were stored at a temperature between 950–975 °C, at a pressure between 700–1500 bars, and with
a water content of 3.0–5.0 wt%. A hornblende andesite (spessartite) from Mascota, of nearly identical composition but with
only amphibole phenocrysts, had a similar temperature but equilibrated at a minimum of 2000 bars pressure with a dissolved
water content of at least 5.5 wt% in the liquid. Experiments on the basaltic andesite show that the most common natural phenocryst
assemblages (olivine, ±augite, ±plagioclase) could have precipitated at temperatures from 1000–1150 °C, in liquids with a
wide range of dissolved water content (∼2.0–6.0 wt%) and a corresponding pressure range. A lava of the same bulk composition
with phenocrysts of hornblende, olivine, plagioclase, and augite is restricted to temperatures below 1000 °C and pressures
below 2500 bars, corresponding to <5.5 wt% water in the residual liquid. Although there is some evidence for mixing in the
andesites (sporadic olivine phenocrysts), the broad theme of the history of both lava types is that the phenocryst assemblages
for both the andesitic magmas and basaltic andesitic magmas are generated from degassing and reequilibration on ascent of
initially hydrous parents containing greater than 6 wt% water. Indeed andesitic magmas could be related to a basaltic andesite
parent by hornblende-plagioclase fractionation under the same hydrous conditions.
Received: 10 December 1996 / Accepted: 21 August 1997 相似文献
2.
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
3.
Summary Mafic microgranular enclaves in the ultrapotassic Piquiri Syenitic Massif (611 ± 1 Ma) in southern Brazil represent a minette
magma mingled with a syenitic one, both produced from similar mantle sources and emplaced in a post-collisional setting of
Neoproterozoic age. The minette magma is compositionally close to typical minettes and high-SiO2 lamproites, with relatively high contents of LREE, Cs and Rb. It is slightly silica-undersaturated, ultrapotassic and metaluminous,
with K2O/Na2O ratios around 2–3, and about 4–7 wt% K2O. The Piquiri minettes contain K-clinopyroxene and pyrope, which are interpreted to have crystallized under pressures about
5 GPa. Whole-rock and mineral chemistry indicate that the most suitable source for the minette magma is clinopyroxene-phlogopite-apatite-amphibole-sulphide
± garnet mantle veins, under pressures of about 5 GPa and melting temperatures over 1,000 °C. Fractional melting is admitted
in order to explain the extremely high Rb, Cs and LREE contents of the minette melt, and is consistent with its estimated
rheological behavior. The syenitic host-rock parental magma was produced from a similar source, probably at lower pressures,
and the co-mingling probably occurred still at large depth, under pressures around 3 GPa. Rheological and geochemical considerations
support a model based on fractional melting of a veined mantle which had been metasomatized during previous (760–700 Ma) ocean-plate
consumption. The subduction-related metasomatism in the source is indicated by low LREE/(Nb or Ta) ratios, high Nb/Ta and
U/Th ratios, and low Ti contents. The compositional similarity and close spatial and temporal association of minette and syenitic
magmas can be explained by their common source region. Compared to typical lamproitic magmatism, the major difference is that
the Piquiri minette magmas are derived from a subduction-modified source. 相似文献
4.
Experimental melting relationships for a mafic minette (mica-lamprophyre) from Buell Park, Arizona were determined under fO2 conditions equivalent to the ironwüstite-graphite and quartz-fayalite-magnetite buffers, at pressures of 10–20 kbar. A comparison between experimental products and phenocrysts in the most primitive minettes indicates that those lavas preserve a near-liquidus assemblage of olivine, diopside and Ti-rich phlogopite crystallized in the upper mantle under fO2QFM and in the presence of an H2O-bearing fluid phase. It is suggested that micalamprophyric (minette) magmas may originate from a metasomatized, garnet-bearing peridotitic source at deeper levels in the mantle (P20 kbar) but can also be in equilibrium with a phlogopite-bearing wehrlite (±opx) source at pressures of 17–20 kbar, under reducing or oxidizing mantle conditions. Owing to their rapid crystallization rate and high liquidus temperatures, a series of potassic daughter melts (potassic latites and felsic minettes) can be formed by segregation from mafic minette parents during their ascent through the cooler continental crust. The preservation of olivine in equilibrium with phlogopite phenocrysts in primitive minettes precludes a petrogenetic process dominated by assimilation/fractional crystallization in a shallow magma chamber and supports a model by which some lamprophyric magmas are brought to near surface conditions at temperatures in the range of 1,000–1,200° C and chilled rapidly. 相似文献
5.
Fluid inclusions have been studied in three pegmatite fields in Galicia, NW Iberian Peninsula. Based on microthermometry
and Raman spectroscopy, eight fluid systems have been recognized. The first fluid may be considered to be a pegmatitic fluid
which is represented by daughter mineral (silicates)-rich aqueous inclusions. These inclusions are primary and formed above
500 °C (dissolution of daughter minerals). During pegmatite crystallization, this fluid evolved to a low-density, volatile-rich
aqueous fluid with low salinity (93% H2O; 5% CO2; 0.5% CH4; 0.2% N2; 1.3% NaCl) at minimum P–T conditions around 3 ± 0.5 kbar and 420 °C. This fluid is related to rare-metal mineralization. The volatile enrichment may
be due to mixing of magmatic fluids and fluids equilibrated with the host rock. A drop in pressure from 3 ± 0.5 to 1 kbar
at a temperature above 420 °C, which may be due to the transition from predominantly lithostatic to hydrostatic pressure,
is recorded by two-phase, water-rich inclusions with a low-density vapour phase (CO2, CH4 and N2). Another inclusion type is represented by two-phase, vapour-rich inclusions with a low-density vapour phase (CO2, CH4 and N2), indicating a last stage of decreasing temperature (360 °C) and pressure (around 0.5 kbar), probably due to progressive
exhumation. Finally, volatile (CO2)-rich aqueous inclusions, aqueous inclusions (H2O-NaCl) and mixed-salt aqueous inclusions with low Th, are secondary in charac- ter and represent independent episodes of hydrothermal fluid circulation below 310 °C and 0.5 kbar.
Received: 14 October 1999 / Accepted: 5 October 1999 相似文献
6.
Jürgen Konzett 《Contributions to Mineralogy and Petrology》1997,128(4):385-404
Experiments have been conducted in a peralkaline Ti-KNCMASH system representative of MARID-type bulk compositions to delimit
the stability field of K-richterite in a Ti-rich hydrous mantle assemblage, to assess the compositional variation of amphibole
and coexisting phases as a function of P and T, and to characterise the composition of partial melts derived from the hydrous assemblage. K-richterite is stable in experiments
from 0.5 to 8.0 GPa coexisting with phlogopite, clinopyroxene and a Ti-phase (titanite, rutile or rutile + perovskite). At
8.0 GPa, garnet appears as an additional phase. The upper T stability limit of K-richterite is 1200–1250 °C at 4.0 GPa and 1300–1400 °C at 8.0 GPa. In the presence of phlogopite, K-richterite
shows a systematic increase in K with increasing P to 1.03 pfu (per formula unit) at 8.0 GPa/1100 °C. In the absence of phlogopite, K-richterite attains a maximum of 1.14 K
pfu at 8.0 GPa/1200 °C. Titanium in both amphibole and mica decreases continuously towards high P with a nearly constant partitioning while Ti in clinopyroxene remains more or less constant. In all experiments below 6.0 GPa
ΣSi + Al in K-richterite is less than 8.0 when normalised to 23 oxygens+stoichiometric OH. Rutiles in the Ti-KNCMASH system
are characterised by minor Al and Mg contents that show a systematic variation in concentration with P(T) and the coexisting assemblage. Partial melts produced in the Ti-KNCMASH system are extremely peralkaline [(K2O+Na2O)/Al2O3 = 1.7–3.7], Si-poor (40–45 wt% SiO2), and Ti-rich (5.6–9.2 wt% TiO2) and are very similar to certain Ti-rich lamproite glasses. At 4.0 GPa, the solidus is thought to coincide with the K-richterite-out
reaction, the first melt is saturated in a phlogopite-rutile-lherzolite assemblage. Both phlogopite and rutile disappear ca.
150 °C above the solidus. At 8.0 GPa, the solidus must be located at T≤1400 °C. At this temperature, a melt is in equilibrium with a garnet- rutile-lherzolite assemblage. As opposed to 4.0 GPa, phlogopite
does not buffer the melt composition at 8.0 GPa. The experimental results suggest that partial melting of MARID-type assemblages
at pressures ≥4.0 GPa can generate Si-poor and partly ultrapotassic melts similar in composition to that of olivine lamproites.
Received: 23 December 1996 / Accepted: 20 March 1997 相似文献
7.
Fleurice Parat François Holtz Miloš René Renat Almeev 《Contributions to Mineralogy and Petrology》2010,159(3):331-347
The equilibrium phase relations of a mafic durbachite (53 wt.% SiO2) from the Třebíč pluton, representative of the Variscan ultrapotassic magmatism of the Bohemian Massif (338–335 Ma), have
been determined as a function of temperature (900–1,100°C), pressure (100–200 MPa), and H2O activity (1.1–6.1 wt.% H2O in the melt). Two oxygen fugacity ranges were investigated: close to the Ni–NiO (NNO) buffer and 2.6 log unit above NNO
buffer (∆NNO + 2.6). At 1,100°C, olivine is the liquidus phase and co-crystallized with phlogopite and augite at 1,000°C for
the whole range of investigated pressure and water content in the melt. At 900°C, the mineral assemblage consists of augite
and phlogopite, whereas olivine is not stable. The stability field of both alkali feldspar and plagioclase is restricted to
low pressure (100 MPa) at nearly water-saturated conditions (<3–4 wt.% H2O) and T < 900°C. A comparison between experimental products and natural minerals indicates that mafic durbachites have a near-liquidus
assemblage of olivine, augite, Ti-rich phlogopite, apatite and zircon, followed by alkali feldspar and plagioclase, similar
to the mineral assemblage of minette magma. Natural amphibole, diopside and orthopyroxene were not reproduced experimentally
and probably result from sub-solidus reactions, whereas biotite re-equilibrated at low temperature. The crystallization sequence
olivine followed by phlogopite and augite reproduces the sequence inferred in many mica-lamprophyre rocks. The similar fractionation
trends observed for durbachites and minettes indicate that mafic durbachites are probably the plutonic equivalents of minettes
and that K- and Mg-rich magmas in the Bohemian Massif may have been generated from partial melting of a phlogopite–clinopyroxene-bearing
metasomatized peridotite. Experimental melt compositions also suggest that felsic durbachites can be generated by simple fractionation
of a more mafic parent and mixing with mantle-derived components at mid crustal pressures. 相似文献
8.
Andrea Orlando Yves Thibault Alan D. Edgar 《Contributions to Mineralogy and Petrology》2000,139(2):136-145
Experiments ranging from 2 to 3 GPa and 800 to 1300 °C and at 0.15 GPa and 770 °C were performed to investigate the stability
and mutual solubility of the K2ZrSi3O9 (wadeite) and K2TiSi3O9 cyclosilicates under upper mantle conditions. The K2ZrSi3O9–K2TiSi3O9 join exhibits complete miscibility in the P–T interval investigated. With increasing degree of melting the solid solution becomes progressively enriched in Zr, indicating
that K2ZrSi3O9 is the more refractory end member. At 2 GPa, in the more complex K2ZrSi3O9–K2TiSi3O9–K2Mg6Al2Si6O20(OH)4 system, the presence of phlogopite clearly limits the extent of solid solution of the cyclosilicate to more Zr-rich compositions
[Zr/(Zr + Ti) > 0.85], comparable to wadeite found in nature, with TiO2 partitioning strongly into the coexisting mica and/or liquid. However, at 1200 °C, with increasing pressure from 2 to 3 GPa,
the partitioning behaviour of TiO2 changes in favour of the cyclosilicate, with Zr/(Zr + Ti) of the K2(Zr,Ti)Si3O9 phase decreasing from ∼0.9 to ∼0.6. The variation in the Ti content of the coexisting phlogopite is related to its degree
of melting to forsterite and liquid, following the major substitution VITi+VI□=2VIMg.
Received: 26 January 1999 / Accepted: 10 January 2000 相似文献
9.
K. Putirka Marie Johnson Rosamond Kinzler John Longhi David Walker 《Contributions to Mineralogy and Petrology》1996,123(1):92-108
Models for estimating the pressure and temperature of igneous rocks from co-existing clino-pyroxene and liquid compositions
are calibrated from existing data and from new data obtained from experiments performed on several mafic bulk compositions
(from 8–30 kbar and 1100–1475° C). The resulting geothermobarometers involve thermodynamic expressions that relate temperature
and pressure to equilibrium constants. Specifically, the jadeite (Jd; NaAlSi2O6)–diopside/hedenbergite (DiHd; Ca(Mg, Fe) Si2O6) exchange equilibrium between clinopyroxene and liquid is temperature sensitive. When compositional corrections are made
to the calibrated equilibrium constant the resulting geothermometer is
(i) 104
T=6.73−0.26* ln [Jdpx*Caliq*FmliqDiHdpx*Naliq*Alliq] −0.86* ln [MgliqMgliq+Feliq]+0.52*ln [Caliq]
an expression which estimates temperature to ±27 K. Compared to (i), the equilibrium constant for jadeite formation is more
sensitive to pressure resulting in a thermobarometer
(ii) P=−54.3+299* T104+36.4* T104 ln [Jdpx[Siliq]2*Naliq*Alliq] +367*[Naliq*Alliq]
which estimates pressure to ± 1.4 kbar. Pressure is in kbar, T is in Kelvin. Quantities such as Naliq represent the cation fraction of the given oxide (NaO0.5) in the liquid and Fm=MgO+FeO. The mole fractions of Jd and diopside+hedenbergite (DiHd) components are calculated from a
normative scheme which assigns the lesser of Na or octahedral Al to form Jd; any excess AlVI forms Calcium Tschermak’s component (CaTs; CaAlAlSiO6); Ca remaining after forming CaTs and CaTiAl2O6 is taken as DiHd. Experimental data not included in the regressions were used to test models (i) and (ii). Error on predictions
of T using model (i) is ±40 K. A pressure-dependent form of (i) reduces this error to ±30 K. Using model (ii) to predict pressures,
the error on mean values of 10 isobaric data sets (0–25 kbar, 118 data) is ±0.3 kbar. Calculating thermodynamic properties
from regression coefficients in (ii) gives VJd
f of 23.4 ±1.3 cm3/mol, close to the value anticipated from bar molar volume data (23.5 cm3/mol). Applied to clinopyroxene phenocrysts from Mauna Kea, Hawaii lavas, the expressions estimate equilibration depths as
great as 40 km. This result indicates that transport was sufficiently rapid that at least some phenocrysts had insufficient
time to re-equilibrate at lower pressures.
Received: 16 May 1994/Accepted: 15 June 1995 相似文献
10.
An experimental study of a minette from the Milk River area, southern Alberta, Canada 总被引:1,自引:1,他引:0
Buhlmann et al. (Can J Earth Sci 37: 1629–1650, 2000) studied the minettes and xenoliths from the Milk River area of southern Alberta, Canada. Based on previous work, they hypothesized that the minettes were derived from a source containing phlogopite?+?clinopyroxene?±?olivine, at pressures ≥1.7?GPa. To test this hypothesis, liquidus experiments were performed on a primitive minette between 1.33 and 2.21?GPa and between 1,300 and 1,400?°C to constrain the mineralogy of its source region. We found a multiple saturation point along the liquidus at 1.77 GPa and 1,350?°C, where the liquid coexists with orthopyroxene and olivine. Neither phlogopite nor clinopyroxene were found to be liquidus phases, which is inconsistent with Buhlmann et al.’s hypothesis. We suggest that our minette is not primary, but had re-equilibrated with harzburgitic mantle subsequent to formation. In such a scenario, partial melting of a veined source containing mica and clinopyroxene occurred at or near the base of the Wyoming craton (~200?km). Minimal heating or the introduction of hydrous fluids into the source would be required to induce partial melting. Rapid ascent rates, coupled with slow cooling rates, of the “primary minette magma” would preserve the high temperature observed in our experiments. At ~58?km, our “primary minette magma” likely stalled and re-equilibrated with the harzburgite surroundings. 相似文献
11.
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
12.
J. L. Rosenberg P. G. Spry C. E. Jacobson N. J. Cook F. M. Vokes 《Mineralium Deposita》1998,34(1):19-34
The Bleikvassli massive sulfide ore deposit is hosted by Proterozoic pelitic, quartzofeldspathic, and amphibolitic rocks
of the Uppermost Allochthon of the Scandinavian Caledonides. Staurolite-garnet-biotite and kyanite-staurolite-biotite assemblages
indicate that metamorphism reached the kyanite zone of the amphibolite facies. Geothermobarometry was conducted on rocks in
and around the deposit using a variety of silicate and sulfide calibrations. Temperature determinations are most reliant on
the garnet-biotite exchange reaction, with analyses obtained from 259 garnet rims and adjacent biotite. Results from nine
calibrations of the garnet-biotite geothermometer are considered, but compositional limitations of many calibrations involving
high Ca and Mn contents in garnet and AlVI and Ti in biotite make many of the coexisting mineral pairs unsuitable. Average temperatures calculated from the two calibrations
that most closely address the garnet-biotite compositions observed at Bleikvassli are 584 °C ± 49 °C and 570 °C ± 40 °C. The
application of two calibrations of the garnet-staurolite geothermometer on a limited number of samples yields 581 °C ± 2 °C
and 589 °C ± 12 °C, assuming a
H2O=0.84, based upon calculations of the modal proportions of gaseous species. Pressure determinations are less constrained.
Phengite and plagioclase-biotite-garnet-muscovite geobarometers give average pressures of approximately 5.0 kbar and 8.5 ± 1.2 kbar,
respectively. Pressures obtained from the sphalerite-hexagonal pyrrhotite-pyrite barometer average 7.7 ± 1.0 kbar. In consideration
of these results, the peak metamorphic conditions at the Bleikvassli deposit are estimated to be 580 °C and 8 kbar.
Received: 18 June 1997 / Accepted: 14 May 1998 相似文献
13.
MACDONALD R.; UPTON B. G. J.; COLLERSON K. D.; HEARN B. C. HEARN Jr.; JAMES D. 《Journal of Petrology》1992,33(2):305-346
The volcanic rocks of the Bearpaw Mountains are part of theMontana high-potassium province, emplaced through Archaean rocksof the Wyoming Craton between 54 and 50 Ma ago. Extrusive rocks,dominated by minettes and latites, have a volume of 825 km3.The minettes range in composition from 20 to 6% MgO. The moremagnesian varieties contain the phenocryst assemblage forsterite+ Cr-spinel + diopside phlogopite. More evolved rocks areolivine-free, with an assemblage of either salite + phlogopite+ pseudoleucite or salite + phlogopite + analcime. The analcimeis thought to be secondary after leucite, produced by loss ofpotassium from the minettes. Mineral chemistry and textures,especially of clinopyroxenes, indicate that mixing between minettemagmas of varying degrees of evolution was commonplace. Compositionalvariation was further extended by accumulation of olivine +spinel + clinopyroxene phenocrysts, and by the preservationof mantle xenocrysts in the minettes. The primary minette magmasare inferred to have had 1214% MgO and to have been generatedat 30 kb from an olivine + diopside + phlogopite-bearing source.The primary magmas evolved dominantly by fractionation of olivine+ diopside. The minettes have high contents of large ion lithophile elements(LILE) and light rare earth elements (LREE), with K2O up to6.18%, Ba 5491 ppm, Sr 2291 ppm, and Ce 99 ppm. (87Sr/86Sr)0ranges from 0.707 to 0.710 and Nd varies from 10 to16. These data, plus high LILE/HFSE (high field strengthelements) values, are interpreted to show that the minettescontain at least three different mantle components. The lithospherewas initially depleted in Archaean times, but was metasomaticallyenriched in the Proterozoic and in the late Cretaceous and earlyTertiary. The latites have many chemical features in common with the minettes,such as potassic character and high LILE/HFSE values. They formedby fractional crystallization of minette magma in combinationwith assimilation of crustal rocks; this process enriched themagmas in SiO2 and raised Na2O/K2O and 87Sr/86Sr values. Chemicaldata for phenocrysts and bulk rocks in minettes suggest mixingbetween minette and latite magmas. 相似文献
14.
The Archean Shawmere anorthosite lies within the granulite facies portion of the Kapuskasing Structural Zone (KSZ), Ontario,
and is crosscut by numerous linear alteration veins containing calcite + quartz ± dolomite ± zoisite ± clinozoisite ± margarite ±paragonite ± chlorite.
These veins roughly parallel the trend of the Ivanhoe Lake Cataclastic Zone. Equilibria involving clinozoisite + margarite + quartz ± calcite
± plagioclase show that the vein minerals were stable at T < 600 °C, XCO2 < 0.4 at P ≈ 6 kbar. The stabilities of margarite and paragonite in equilibrium with quartz are also consistent with T < 600 °C and XCO2 < 0.4 at 6 kbar. Additional assemblages consisting of calcite + clinochlore + quartz + talc + margarite indicate T < 500 °C with XCO2 > 0.9. Thus, vein formation, while clearly retrograde, spanned a range of temperatures, and fluid compositions evolved from
H2O-rich to CO2-rich. The calcite in the retrograde veins has δ18O values that range from 8.4 to 11.2‰ (average = +9.7 ± 0.9‰) and δ13C values that range from −3.9 to −1.6‰ (average = −3.1 ± 0.6‰). These values indicate that the fluids from which calcite precipitated
underwent extensive exchange with the anorthosite and other crustal lithologies. The fluids may have been initially derived
either from devolatilization of metamorphic rocks or crystallization of igneous rocks in the adjacent Abitibi subprovince.
Vein quartz contains CO2-rich fluid inclusions (final melting T = −57.0 to −58.7 °C) that range in size from 5 to 17 μm. Measured homogenization temperatures (T h) range from −44.0 to 14.5 °C, however for most inclusions (46 of S1), T h = −44.0 to −21.1 °C (ρCO2 ≈ 1.13 to 1.05 g/cm3). At 400 to 600 °C, these densities correspond to pressures of 3.5 to 7 kbar, which is the best estimate of pressures of
vein formation. It has been argued that some high density CO2-rich fluid inclusions found in the KSZ were formed during peak metamorphism and thus document the presence of a CO2-rich fluid during peak granulite facies metamorphism (Rudnick et al. 1984). The association of high density CO2-rich fluid inclusions with clearly retrograde veins documents the formation of similar composition and density inclusions
after the peak of metamorphism. Thus, the coincidence of entrapment pressures calculated from fluid inclusion density measurements
with peak metamorphic pressures alone should not be considered strong evidence for peak metamorphic inclusion entrapment.
All fluid inclusion results are consistent with an initially semi-isobaric retrograde P–T path.
Received: 2 April 1996 / Accepted: 15 November 1996 相似文献
15.
E. Schmädicke M. Okrusch W. Schubert B. Elwart U. Görke 《Mineralogy and Petrology》2001,72(1-3):77-111
Summary In the Odenwald Crystalline Complex, calc-silicate rocks are concentrated at the margins of the marble layer of Auerbach.
They were presumably formed by metasomatic exchange between the calcite marble and the neighbouring granodioritic and quartz-dioritic
intrusives. The investigated samples contain the characteristic mineral assemblages: garnet + clinopyroxene + epidote/clinozoisite + calcite + quartz ± titanite
(1) and wollastonite + clinopyroxene + garnet + calcite ± quartz ± epidote/clinozoisite ± titanite (2). Microprobe analyses
revealed the following compositional ranges: garnet grs40–98adr2–55alm<5.5sps<5.5pyp<1; clinopyroxene di46–88hed9–47joh0–5cats0–6; epidote/clinozoisite ps20–80. Different phase diagrams were calculated in the system CaO-MgO-Al2O3-TiO2-SiO2-CO2-H2O (CMATSCH) to decipher the P-T-XCO2 parameters of metamorphism: isobaric T-XCO2 sections and a P-T projection with mixed volatiles. The phase diagrams illustrate that the observed assemblages can only
form in the presence of an H2O-rich volatile phase. The assemblages are stable over a large range of temperatures, from 580 °C to < 400 °C (at 4 kbar)
and at XCO2 values of less than 0.055 (at 4 kbar). Higher temperatures can be inferred from reaction textures which indicate that garnet + plagioclase
(T > 580 °C, at 4 kbar) and wollastonite + plagioclase (T > 660 °C, at 4 kbar) coexisted during an early metamorphic stage. A minimum pressure of 3.5 kbar can be inferred for the
early high-temperature stage. Furthermore, on the basis of the calculated phase diagrams, combined with modal abundances in
thin sections, it is possible to evaluate fluid behaviour; in the investigated specimens, infiltration of fluids from an external
reservoir occurred. A minimum fluid:rock ratio of 3.6:1 can be estimated.
Received July 29, 1999; accepted March 28, 2000 相似文献
Zusammenfassung Phasenbeziehungen in Kalksilikat-Paragenesen des Marmorzuges von Auerbach, Odenwald-Kristallin-Komplex, Deutschland Im kristallinen Odenwald konzentrieren sich kalksilikatische Gesteine in den Randbereichen des Marmorzuges von Auerbach. Die kalksilikatischen Partien wurden vermutlich duch metasomatischen Austausch zwischen dem Calcit-Marmor und benachbarten Granodioriten und Quarzdioriten gebildet. Die untersuchten Proben enthalten die charakteristischen Mineralparagenesen: Granat + Klinopyroxen + Epidot/Klinozoisit + Calcit + Quarz + Titanit (1) und Wollastonit + Klinopyroxen + Granat + Calcit ± Quarz ± Epidot/Klinozoisit ± Titanit (2). Mikrosondenanalysen ergaben folgendes Zusammensetzungsspektrum: Granat grs40–98adr2–55alm<5.5sps<5.5pyp<1; Klinopyroxen di46–88hed9–47joh0–5cats0–6s; Epidot/Klinozoisit ps20–80. Verschiedene Phasendiagramme wurden für das Modellsystem CaO-MgO-Al2O3-TiO2-SiO2-CO2-H2O (CMATSCH) berechnet, um die P-T-XCO2-Parameter der Metamorphose einzugrenzen: Isobare T-XCO2-Schnitte und eine P-T-Projektion mit einer Fluid-Mischphase. Die Phasendiagramme verdeutlichen, da? die beobachteten Paragenesen nur in Anwesenheit eines H2O-reichen Fluids gebildet werden k?nnen. Die Paragenesen sind über einen gro?en Temperaturbereich hinweg stabil, von 580 °C bis < 400 °C (bei 4 kbar) und bei XCO2-Gehalten von < 0.055 (bei 4 kbar). Ursprünglich h?here Temperaturen k?nnen anhand von Reaktions-Texturen rekonstruiert werden, die zeigen, da? Granat + Plagioklas (T > 580 °C, bei 4 kbar) und Wollastonit + Plagioklas (T > 660 °C, bei 4 kbar) w?hrend eines früheren Metamorphosestadiums koexistierten. Ein Minimaldruck von 3.5 kbar kann für dieses frühe Hochtemperatur-Stadium abgeleitet werden. Mit Hilfe der berechneten Phasendiagramme, in Kombination mit beobachteten Modalgehalten, ist es m?glich, das Verhalten der fluiden Phase abzusch?tzen. Die untersuchten Gesteine implizieren Fluidinfiltration, wobei ein minimales Verh?ltnis Fluid:Gestein von 3.6:1 abgesch?tzt werden kann.
Received July 29, 1999; accepted March 28, 2000 相似文献
16.
Fabrice Brunet Christian Chopin Friedrich Seifert 《Contributions to Mineralogy and Petrology》1998,131(1):54-70
The polymorphic relations for Mg3(PO4)2 and Mg2PO4OH have been determined by reversed experiments in the temperature-pressure (T-P) range 500–1100 °C, 2–30 kbar. The phase transition between the low-pressure phase farringtonite and Mg3(PO4)2-II, the Mg analogue of sarcopside, is very pressure dependent and was tightly bracketed between 625 °C, 7 kbar and 850 °C,
9 kbar. The high-temperature, high-pressure polymorph, Mg3(PO4)2-III, is stable above 1050 °C at 10 kbar and above 900 °C at 30 kbar. The low-pressure stability of farringtonite is in keeping
with its occurrence in meteorites. The presence of iron stabilizes the sarcopside-type phase towards lower P. From the five Mg2PO4OH polymorphs only althausite, holtedahlite, β-Mg2PO4OH (the hydroxyl analogue of wagnerite) and ɛ-Mg2PO4OH were encountered. Relatively speaking, holtedahlite is the low-temperature phase (<600 °C), ɛ-Mg2PO4OH the high-temperature, low-pressure phase and β-Mg2PO4OH the high-temperature, high-pressure phase, with an intervening stability field for althausite which extends from about
3 kbar at 500 °C to about 12 kbar at 800 °C. Althausite and holtedahlite are to be expected in F-free natural systems under
most geological conditions; however, wagnerite is the most common Mg-phosphate mineral, implying that fluorine has a major
effect in stabilizing the wagnerite structure. Coexisting althausite and holtedahlite from Modum, S. Norway, show that minor
fluorine is strongly partitioned into althausite (KD
F/OH≈ 4) and that holtedahlite may incorporate up to 4 wt% SiO2. Synthetic phosphoellenbergerite has a composition close to (Mg0.9□0.1)2Mg12P8O38H8.4. It is a high-pressure phase, which breaks down to Mg2PO4OH + Mg3(PO4)2 + H2O below 8.5 kbar at 650 °C, 22.5 kbar at 900 °C and 30 kbar at 975 °C. The stability field of the phosphate end-member of
the ellenbergerite series extends therefore to much lower P and higher T than that of the silicate end-members (stable above 27 kbar and below ca. 725 °C). Thus the Si/P ratio of intermediate members
of the series has a great barometric potential, especially in the Si-buffering assemblage with clinochlore + talc + kyanite
+ rutile + H2O. Application to zoned ellenbergerite crystals included in the Dora-Maira pyrope megablasts, western Alps, reveals that growth
zoning is preserved at T as high as 700–725 °C. However, the record of attainment of the highest T and/or of decreasing P through P-rich rims (1 to 2 Si pfu) is only possible in the presence of an additional phosphate phase (OH-bearing or even
OH-dominant wagnerite in these rocks), otherwise the trace amounts of P in the system remain sequestered in the core of Si-rich
crystals (5 to 8 Si pfu) and can no longer react.
Received: 7 April 1995 / Accepted: 12 November 1997 相似文献
17.
Eclogitic metasediments from the Tso Morari area (Ladakh, Himalaya): evidence for continental subduction during India-Asia convergence 总被引:9,自引:0,他引:9
S. Guillot J. de Sigoyer J. M. Lardeaux G. Mascle 《Contributions to Mineralogy and Petrology》1997,128(2-3):197-212
Metasediments in the Tso Morari area (Ladakh, Himalaya) provide new insights into the Higher Himalayan metamorphism in the
northwestern part of the Himalayan belt. Whole-rock analyses and petrologic observations show that the metasediments correspond
to Fe-rich metapelites, Mg-rich metapelites, intermediate metapelites and metagreywackes of the Indian continental margin.
Jadeite + chloritoid + paragonite + garnet in the Fe-rich metapelites indicate pressures of 20 ±2 kbar at temperatures of
550 ±50 °C according to major element partitioning thermobarometry, stability fields of minerals and Thermocalc P-T estimates. These results are consistent with P-T estimates on other metasediments and with the occurrence of eclogites. Subsequent retrogression at the eclogite-blueschist
facies transition (from 18 to 13 kbar and 540 ±50 °C) was followed by an increase in temperature to 630 ±30 °C at amphibolite
facies conditions. The metamorphic evolution is related to subduction of the Indian continental margin beneath the southern
Asian margin at the onset of the Indian-Eurasian collision.
Received: 17 April 1996 / Accepted: 19 February 1997 相似文献
18.
Edward S. Grew Nikolai N. Pertsev Stanislav Vrána Martin G. Yates Charles K. Shearer Michael Wiedenbeck 《Contributions to Mineralogy and Petrology》1998,131(1):22-38
Kornerupine, (□,Fe,Mg)(Mg,Fe,Al)9(Si,Al,B)5 (O,OH,F)22, has been reported with talc in rocks from six localities worldwide, but only at Chilapila Hill in the Lufilian Arc, Zambia
do textural relationships imply that kornerupine (Krn) equilibrated with talc (Tlc) during a prograde metamorphic event at
T≈ 640 °C, P≈ 13 kbar; a prograde Krn + Tlc assemblage has also been reported from Mautia Hill, Tanzania (P ≤ 13 kbar). In order to estimate possible constraints on the stability range for the kornerupine + talc paragenesis in nature,
we constructed a P-T diagram in the model system MgO-Al2O3-SiO2-H2O (MASH) for seven phases quartz (Qtz), B-free kornerupine sensu stricto, anthophyllite (Ath), chlorite (Chl), cordierite
(Crd), kyanite (Ky), and talc. The minimum pressure for Krn + Tlc + Ky stability in MASH is close to that for Ky + Tlc stability,
i.e., 6–8 kbar, at T≤ 780 °C. However, in the natural system, B2O3 and Na2O are major constituents in Krn and orthoamphibole (Oam), respectively, and dravitic tourmaline (Tur) is widespread. The critical
assemblage alternative to Krn + Tlc in nature is Tur + Oam. The upper pressure limit of Tur + Ath is determined by the upper
pressure for anthophyllite: 7.7–10.5 kbar at 682–794 °C in the MgO-SiO2-H2O system (Chernosky et al. 1985, Am Mineral 70:223–236), and is undoubtedly higher in the presence of Na2O, CaO, and Al2O3. At three of the six localities, talc is a retrograde phase; nonetheless, it possibly equilibrated with kornerupine on the
retrograde path or during a later metamorphic event at P-T conditions appropriate for Ky + Tlc. At the sixth locality (Mulvoj, southwestern Pamir Mountains, Tajikistan), Krn is found
in the same thin section as talc and kyanite and all three minerals formed during a prograde metamorphic event at T≥ 650 °C, P near 7 kbar. However, Krn is restricted to a lens 4 to 6 mm thick of phlogopite + anthophyllite + Tur and it does not touch
either talc or kyanite. A reaction relating the Mulvoj and Chilapila Hill (Krn + Tlc + Ky + Qtz + Tur) parageneses is calculated
from compositions in the Mulvoj rock to be 0.40Tur + 2.55Ath + 1.33H2O + 0.27F = Krn + 2.16Tlc + 0.36B2O3 + 0.02Rutile + 0.19Na2O + 0.17CaO. Given the difference in metamorphic pressures estimated for Mulvoj and Chilapila Hill, Krn + Tlc is inferred
to be favored by increasing pressure as well as by low Na2O and CaO contents. Some FeO, F, Fe2O3, and BeO are present in measurable amounts in at least one of the phases in the Mulvoj and Chilapila Hill whiteschists (e.g.,
Krn contains 0.24–0.67 wt% BeO), but the effect of these constituents is subordinate to that of Na2O, CaO and B2O3. The Krn + Tlc could be a more important assemblage in B-bearing whiteschists than has been reported to date, particularly
at pressures where orthoamphibole is no longer stable.
Received: 21 April 1997 / Accepted: 13 October 1997 相似文献
19.
An alkali basalt near Glen Innes, northeastern New South Wales, contains a suite of Cr-diopside group ultramafic xenoliths
which includes some spinel peridotites but which is dominated by a diverse spinel pyroxenite assemblage. Pyroxenite xenoliths
range from subcalcic clinopyroxenites (composed largely of unmixed prismatic subcalcic clinopyroxene megacrystals and lesser
orthopyroxene megacrystals) to equant mosaic textured websterites (orthopyroxene and Ca-rich clinopyroxene ± spinel). Rare
orthopyroxenite xenoliths also occur. The pyroxenite xenoliths are characterised by high 100Mg/(Mg + Fe2+) ratios (M˜ 90) and low concentrations of Ti, K, P, La, Ce and Zr. The websterites are mineralogically and chemically similar to many
spinel pyroxenites occurring as layers or dykes in peridotite massifs such as those at Ronda in southern Spain and at Ariège
(French Pyrénées). T / P estimates indicate crystallization temperatures of 1250–1350 °C for subcalcic clinopyroxene-orthopyroxene megacrystal pairs
and 900–1000 °C for the equilibrated mosaic textured websterites and associated peridotites at pressures of 9–13 kbar. Subcalcic
clinopyroxene megacrystals, websterites and orthopyroxenites have LREE-depleted chondrite-normalised REE abundances with (La/Yb)CN < 1 and their convex-upwards REE patterns are typical of subcalcic clinopyroxene-dominated cumulates. The pyroxenites are
not residua from partially melted pyroxenite layers or dykes in mantle peridotites nor are they completely crystallized protobasaltic
or protopicritic magmas. They are interpreted as high-pressure crystal segregations from basaltic magmas (probably mildly
alkaline or transitional) flowing within narrow mantle conduits (the flow crystallization model of Irving, 1980). The parental
magma(s) was Ti-poor (0.6–0.7% TiO2) and relatively Mg-rich (M˜ 74 − 70). Pyroxenite genesis was a two-stage process involving crystallization of tschermakitic subcalcic clinopyroxenes
and orthopyroxenes ±spinel as liquidus or near-liquidus phases at 1250–1350 °C and 9–13 kbar to yield “primary” subcalcic
clinopyroxenites which then re-equilibrated at 900–1000 °C and similar pressures to produce the mosaic textured “secondary”
websterites. The pyroxenites show a wide range of 143Nd/144Nd and 87Sr/86Sr values (0.513298–0.512473 and 0.702689–0.704659, respectively). Their isotopic ratios appear to have been variably modified
by exchange with adjacent mantle peridotites or migrating basaltic melts.
Received: 11 December 1995 / Accepted: 3 December 1996 相似文献
20.
Liquidus temperatures and phase compositions in the system Qz-Ab-Or at 5 kbar and very low water activities 总被引:1,自引:0,他引:1
Andreas Becker Francois Holtz Wilhelm Johannes 《Contributions to Mineralogy and Petrology》1998,130(3-4):213-224
Liquidus phase relations have been experimentally determined in the systems Qz-Ab-Or-(H2O), Qz-Ab-(H2O) and Qz-Or-(H2O) at H2O-undersaturated conditions (a
H2O = 0.07) and P = 5 kbar. Starting materials were homogeneous synthetic glasses containing 1 wt% H2O. The liquidus temperatures were bracketed by crystallization and dissolution experiments. The results of kinetic studies
showed that crushed glasses are the best starting materials to overcome undercooling and to minimize the temperature difference
between the lowest temperature of complete dissolution (melting) and the highest temperature at which crystallization can
be observed. At P = 5 kbar and a
H2O = 0.07, the Qz-Ab eutectic composition is Qz32Ab68 at 1095 °C (±10 °C) and the Qz-Or eutectic is Qz38Or62 at 1030 °C (±10 °C). The minimum temperature of the ternary system Qz-Ab-Or is 990 °C (±10 °C) and the minimum composition
is Qz32Ab35‐ Or33. The Qz content of the minimum composition in the system Qz-Ab-Or-H2O remains constant with changing a
H2O. The normative Or content, however, increases by approximately 10 wt% with decreasing a
H2O from 1 to 0.07. Such an increase has already been observed in the system Qz-Ab-Or-H2O-CO2 at high a
H2O and it is concluded that the use of CO2 to reduce water activities does not influence the composition of the minima in quartz-feldspar systems. The determined liquidus
temperature in melts with 1 wt% H2O is very similar to that obtained in previous nominally “dry” experiments. This discrepancy is interpreted to be due to problems
in obtaining absolutely dry conditions. Thus, the hitherto published solidus and liquidus temperatures for “dry” conditions
are probably underestimated.
Received: 27 March 1997 / Accepted: 1 October 1997 相似文献