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1.
Calc-silicate granulites from Rayagada, north-central sector of Eastern Ghats granulite belt show a wide range of mineral
assemblages and chemical compositions, which can be grouped as Gr. I (grossular- rich garnet-wollastonite-scapolite-calcite-clinopyroxene),
Gr. II (andradite-rich garnet-scapolite-calcite-clinopyr- oxene), and Gr. III (scapolite-calcite-clinopyroxene-plagioclase)
assemblages. Petrographic features suggest the following several reactions in the CaO–Al2O3–SiO2-vapor system: Mei+4Wo+Cal=3Grs+Qtz +2CO2, Mei+3Wo+2Cal=3Grs+CO2, Mei= 3An+Cal, Wo+CO2=Cal+Qtz, Mei+5Wo =3Grs+2Qtz+CO2, An+Wo=Grs+Qtz, Mei+ 5Cal+3Qtz=3Grs+6CO2, and the following reactions in the CaO–FeO–MgO–Al2O3–SiO2-vapor system: Cpxss+Scp+Wo=Grtss+Qtz+CO2, 4Hd+ 2Cal+O2=2Adr+2Qtz+2CO2, Cpxss+Scp= Grtss+Cal+Qtz. These reactions have been used to estimate peak T-X
CO2 condition for these granulites. A maximum temperature of ∼920 °C has been calculated at an estimated pressure of 9 kbar.
A T-X
CO2 diagram shows an isobaric cooling from ∼920 °C to ∼815 °C. A range of X
CO2 (0.50 at 920 °C to 0.25 at 815 °C) has been observed for Gr. I calc-silicate granulites based on the reaction sequences including
coronal garnet-forming reactions. This sequence is suggestive of internal fluid buffering rather than external fluid influx
and the differences in X
CO2 conditions has been thought to be due to local buffering of fluid phases. Group II and Gr. III calc-silicate granulites,
on the other hand, exhibit relatively lower temperature conditions.
Received: 11 September 1995/Accepted: 20 June 1996 相似文献
2.
John M. Ferry 《Contributions to Mineralogy and Petrology》1996,124(3-4):235-254
Siliceous dolomites and limestones contain abundant retrograde minerals produced by hydration-carbonation reactions as the
aureole cooled. Marbles that contained periclase at the peak of metamorphism bear secondary brucite, dolomite, and serpentine;
forsterite-dolomite marbles have retrograde tremolite and serpentine; wollastonite limestones contain secondary calcite and
quartz; and wollastonite-free limestones have retrograde tremolite. Secondary tremolite never appears in marbles where brucite
has replaced periclase or in wollastonite-bearing limestones. A model for infiltration of siliceous carbonates by CO2-H2O fluid that assumes (a) vertical upwardly-directed flow, (b) fluid flux proportional to cooling rate, and (c) flow and reaction
under conditions of local equilibrium between peak temperatures and ≈400 °C, reproduces the modes of altered carbonate rocks,
observed reaction textures, and the incompatibility between tremolite and brucite and between tremolite and wollastonite.
Except for samples from a dolomite xenolith, retrograde time-integrated flux recorded by reaction progress is on the order
of 1000 mol fluid/cm2 rock. Local focusing of flow near the contact is indicated by samples from the xenolith that record values an order of magnitude
greater. Formation of periclase, forsterite, and wollastonite at the peak of metamorphism also required infiltration with
prograde time-integrated flux approximately 100–1000 mol/cm2. The comparatively small values of prograde and retrograde time-integrated flux are consistent with lack of stable isotope
alteration of the carbonates and with the success of conductive thermal models in reproducing peak metamorphic temperatures
recorded by mineral equilibria. Although isobaric univariant assemblages are ubiquitous in the carbonates, most formed during
retrograde metamorphism. Isobaric univariant assemblages observed in metacarbonates from contact aureoles may not record physical
conditions at the peak of metamorphism as is commonly assumed.
Received: 19 September 1995 / Accepted: 14 March 1996 相似文献
3.
Determination of time-integrated metamorphic fluid fluxes from the reaction progress of multivariant assemblages 总被引:1,自引:1,他引:0
An expression is derived for the calculation of time-integrated metamorphic fluid fluxes in two or more dimensions in rocks
undergoing multivariant reactions under conditions of varying pressure, temperature and angle of flow. This calcuation requires
knowledge of mineral assemblages, modes and compositions, which are obtained from isobaric T-X
CO2 pseudosections constructed using the program THERMOCALC and compared with those observed in east central Vermont. THERMOCALC is capable of reproducing peak mineral assemblages, modes, compositions and the observed reaction sequences within the system
KCaNaFMASCH for two kyanite grade pelitic carbonate rocks from a Barrovian style regional metamorphic terrain in east central
Vermont, U.S.A. Calculation of fluid fluxes for decarbonation reactions under conditions of horizontal, layer-parallel flow
produces time-integrated fluid flux figures of the order of 108 moles m−2. Allowance for possible cross-layer flow from adjacent dehydrating pelites reduces this figure significantly, with episodic
cross-layer fluxes of the order of 105 moles m−2 being capable of driving the observed decarbonation. Chlorite bearing carbonate protoliths would have initially dehydrated
with increasing temperature, a process requiring down-temperature fluid flow to produce the assemblages currently observed.
Received: 28 January 1998 / Accepted: 20 September 1998 相似文献
4.
Periclase formed in steeply dipping marbles from the Beinn an Dubhaich aureole, Scotland, and the Silver Star aureole, Montana,
by the reaction dolomite = periclase + calcite + CO2. Equilibrium between rock and fluids with X
CO
2 < 1 requires that reaction was infiltration-driven. Brucite pseudomorphs after periclase occur in the Beinn an Dubhaich aureole
either as bed-by-bed replacement of dolomite or in a lens along the contact between dolomite and a pre-metamorphic dike. Transport
theory predicts that infiltration drove both periclase reaction and 18O-depletion fronts which moved at significantly different velocities along the flow path. The distributions of brucite and
18O-depleted rocks are identical in surface exposures, thus indicating upward flow. Time-integrated flux (q) was <500 mol/cm2 and the fluid source was magmatic. Because periclase and its hydrated equivalent brucite are unaltered to dolomite by retrograde
reactions, the exposure of brucite marbles accurately images the flow paths of peak metamorphic fluids. In the Silver Star
aureole brucite pseudomorphs after periclase exclusively occur in tabular bodies that are beds with elevated Mg/Ca. The spatial
pattern of 18O-depletion requires upward vertical fluid flow. Estimated prograde q ≈ 103–104 mol/cm2 and the fluid source was magmatic. Low Mg/Ca, 18O-depleted, brucite-free rocks pose a dilemma because the periclase reaction front should have traveled ≈18 times further
through them than the isotope alteration front. The dilemma is resolved by reaction textures that indicate periclase and
brucite were destroyed in low Mg/Ca rocks by infiltration-driven retrograde carbonation reactions. Values of retrograde q were ≈103–104 mol/cm2. Brucite (after periclase) was preserved only in high Mg/Ca layers where periclase developed in greater abundance. The geometry
of brucite marbles at Silver Star thus reflects the location of high Mg/Ca beds rather than the geometry of fluid flow. Retrograde
reactions must be considered before the mineralogical record of prograde fluid flow can correctly be interpreted. In both
aureoles fluid flow, mineral reaction, and isotope depletion were structurally controlled by bedding and lithologic contacts.
Received: 30 July 1996 / Accepted: 21 March 1997 相似文献
5.
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
6.
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
7.
Fluid infiltration and regional metamorphism of the Waits River Formation, north-east Vermont, USA 总被引:2,自引:0,他引:2
Abstract The Siluro-Devonian Waits River Formation of north-east Vermont was deformed, intruded by plutons and regionally metamorphosed during the Devonian Acadian Orogeny. Five metamorphic zones were mapped based on the mineralogy of carbonate rocks. From low to high grade, these are: (1) ankerite-albite, (2) ankerite-oligoclase, (3) biotite, (4) amphibole and (5) diopside zones. Pressure was near 4.5kbar and temperature varied from c. 450° C in the ankerite-albite zone to c. 525° C in the diopside zone. Fluid composition for all metamorphic zones was estimated from mineral equilibria. Average calculated χco2[= CO2/(CO2+ H2O)] of fluid in equilibrium with the marls increases with increasing grade from 0.05 in the ankerite-oligoclase zone, to 0.25 in the biotite zone and to 0.44 in the amphibole zone. In the diopside zone, χCO2 decreases to 0.06. Model prograde metamorphic reactions were derived from measured modes, mineral chemistry, and whole-rock chemistry. Prograde reactions involved decarbonation with an evolved volatile mixture of χCO2 > 0.50. The χCO2 of fluid in equilibrium with rocks from all zones, however, was generally <0.40. This difference attests to the infiltration of a reactive H2O-rich fluid during metamorphism. Metamorphosed carbonate rocks from the formation suggests that both heat flow and pervasive infiltration of a reactive H2O-rich fluid drove mineral reactions during metamorphism. Average time-integrated volume fluxes (cm3 fluid/cm2 rock), calculated from the standard equation for coupled fluid flow and reaction in porous media, are (1) ankerite-oligoclase zone: c. 1 × 104; (2) biotite zone: c. 3 × 104; (3) amphibole zone: c. 10 × 104; and diopside zone: c. 60 × 104. The increase in calculated flux with increasing grade is at least in part the result of internal production of volatiles from prograde reactions in pelitic schists and metacarbonate rocks within the Waits River Formation. The mapped pattern of time-integrated fluxes indicates that the Strafford-Willoughby Arch and the numerous igneous intrusions in the field area focused fluid flow during metamorphism. Many rock specimens in the diopside zone experienced extreme alkali depletion and also record low χCO2. Metamorphic fluids in equilibrium with diopside zone rocks may therefore represent a mixture of acid, H2O-rich fluids given off by the crystallizing magmas, and CO2-H2O fluids produced by devolatilization reactions in the host marls. Higher fluxes and different fluid compositions recorded near the plutons suggest that pluton-driven hydrothermal cells were local highs in the larger regional metamorphic hydrothermal system. 相似文献
8.
Evolution of metamorphic volatiles during exhumation of microdiamond-bearing granulites in the Western Gneiss Region, Norway 总被引:1,自引:0,他引:1
Rune B. Larsen Elizabeth A. Eide Ernst A. J. Burke 《Contributions to Mineralogy and Petrology》1998,133(1-2):106-121
Fluid inclusions in garnet, kyanite and quartz from microdiamond-bearing granulites in the Western Gneiss Region, Norway,
document a conspicuous fluid evolution as the rocks were exhumed following Caledonian high- and ultrahigh-pressure (HP–UHP) metamorphism. The most important of the various fluid mixtures and daughter minerals in these rocks are: (N2 + CO2 + magnesian calcite), (N2 + CO2 + CH4 + graphite + magnesian calcite), (N2 + CH4), (N2 + CH4 + H2O), (CO2) and (H2O + NaCl + CaCl2 + nahcolite). Rutile also occurs in the N2 + CO2 inclusions as a product of titanium diffusion from the garnet host into the fluid inclusions. Volatiles composed of N2 + CO2 + magnesian calcite characterise the ambient metamorphic environment between HP–UHP (peak) and early retrograde metamorphism. During progressive decompression, the mole fraction of N2 increased in the fluid mixtures; as amphibolite-facies conditions were reached, CH4 and later, H2O, appeared in the fluids, concomitant with the disappearance of CO2 and magnesian calcite. Graphite is ubiquitous in the host lithologies and fluid inclusions. Thermodynamic modelling of the
metamorphic volatiles in a graphite-buffered C-O-H system demonstrates that the observed metamorphic volatile evolution was
attainable only if the f
O2 increased from c. −3.5 (±0.3) to −0.8 (±0.3) log units relative to the FMQ oxygen buffer. External introduction of oxidising
aqueous solutions along a system of interconnected ductile shear zones adequately explains the dramatic increase in the f
O2. The oxidising fluids introduced during exhumation were likely derived from dehydration of oceanic crust and continental
sediments previously subducted during an extended period of continental collision in conjunction with the Caledonian orogeny.
Received: 15 December 1997 / Accepted: 25 May 1998 相似文献
9.
High CO2 content of fluid inclusions in gold mineralisations in the Ashanti Belt, Ghana: a new category of ore forming fluids? 总被引:4,自引:0,他引:4
Fluid inclusions were studied in samples from the Ashanti, Konongo-Southern Cross, Prestea, Abosso/Damang and Ayanfuri gold
deposits in the Ashanti Belt, Ghana. Primary fluid inclusions in quartz from mineralised veins of the Ashanti, Prestea, Konongo-Southern
Cross, and Abosso/Damang deposits contain almost exclusively volatile species. The primary setting of the gaseous (i.e. the
fluid components CO2, CH4 and N2) fluid inclusions in clusters and intragranular trails suggests that they represent the mineralising fluids. Microthermometric
and Raman spectroscopic analyses of the inclusions revealed a CO2 dominated fluid with variable contents of N2 and traces of CH4. Water content of most inclusions is below the detection limits of the respective methods used. Aqueous inclusions are rare
in all samples with the exception of those from the granite-hosted Ayanfuri mineralisation. Here inclusions associated with
the gold mineralisation contain a low salinity (<6 eq.wt.% NaCl) aqueous solution with variable quantities of CO2. Microthermometric investigations revealed densities of the gaseous inclusions of 0.65 to 1.06 g/cm3 at Ashanti, 0.85 to 0.98 g/cm3 at Prestea, up to 1.02 g/cm3 at Konongo-Southern Cross, and 0.8 to 1.0 g/cm3 at Abosso/Damang. The fluid inclusion data are used to outline the PT ranges of gold mineralisation of the respective gold deposits. The high density gaseous inclusions found in the auriferous
quartz at Ashanti and Prestea imply rather high pressure trapping conditions of up to 5.4 kbar. In contrast, mineralisation
at Ayanfuri and Abosso/Damang is inferred to have occurred at lower pressures of only up to 2.2 kbar. Mesothermal gold mineralisation
is generally regarded to have formed from fluids characterized by H2O > CO2 and low salinity ( ± 6 eq.wt.%NaCl). However, fluid inclusions in quartz from the gold mineralisations in the Ashanti belt
point to distinctly different fluid compositions. Specifically, the predominance of CO2 and CO2 >> H2O have to be emphasized. Fluid systems with this unique bulk composition were apparently active over more than 200␣km along
strike of the Ashanti belt. Fluids rich in CO2 may present a hitherto unrecognised new category of ore-forming fluids.
Received: 30 May 1996 / Accepted: 8 October 1996 相似文献
10.
L. I. Khodorevskaya 《Petrology》2009,17(4):371-388
The study of metagabbro-norites of the Belomorian Group metamorphosed under the amphibolite-lower granulite facies conditions (Gorelyi Island, Kandalaksha Bay) showed that at contact with Bt-Hbl-Kfs-Pl-Qtz gneiss-granites they were affected by silicic-alkaline H2O-Cl-CO2 brines, which caused the enrichment in alkalis, silica, Rb, Ba, Pb, Zr, LREE and redistribution of Cu, Zn, Cr, Co, V, and Ni along the filtration pathway. The granitization of metagabbro-norite proceeded simultaneously with increase in fluid oxygen fugacity from one log unit below to four log units above QFM. The microprobe determinations of Cl content in biotites and apatites made it possible to calculate variations in the $ f_{H_2 O} The study of metagabbro-norites of the Belomorian Group metamorphosed under the amphibolite-lower granulite facies conditions
(Gorelyi Island, Kandalaksha Bay) showed that at contact with Bt-Hbl-Kfs-Pl-Qtz gneiss-granites they were affected by silicic-alkaline H2O-Cl-CO2 brines, which caused the enrichment in alkalis, silica, Rb, Ba, Pb, Zr, LREE and redistribution of Cu, Zn, Cr, Co, V, and
Ni along the filtration pathway. The granitization of metagabbro-norite proceeded simultaneously with increase in fluid oxygen
fugacity from one log unit below to four log units above QFM. The microprobe determinations of Cl content in biotites and
apatites made it possible to calculate variations in the -f
HCl relations in fluid during its percolation through the rock. It was shown that biotite was formed at metamorphic peak in the
presence of highly aggressive high-f
HCl fluids (log /f
HCl ≈ 0.8–1.2). Apatite was formed in the presence of less acid and more aqueous residual solutions (log /f
HCl ≈ 2.98−3.91), which presumably lost their salt components at metamorphic peak. The calculations showed that the flux of fluid
that percolated through the rock during granitization accounted for q ≈ 4 × 102 to 2 × 103 cm3/cm2. Due to insignificant volume of the fluid, the transformations spanned only marginal part of the metagabbro-norites on Gorelyi
Island.
Original Russian Text ? L.I. Khodorevskaya, 2009, published in Petrologiya, 2009, Vol. 17, No. 4, pp. 397–414. 相似文献
11.
The Ballachulish Igneous Complex consists of an outer quartz diorite and an inner granite, emplaced at about 300 MPa, initially
at 1000 to 1050 °C. The contact aureole (0.5–2 km wide) occurs in metapelites and metapsammites plus minor graphitic slates,
carbonate rocks and metaquartzites. A textural examination of the arkosic Appin Quartzite, which was previously believed to
have melted only within a few metres of the intrusion, demonstrates that partial melting occurred up to 500 m away from the
vertical eastern contact. Coupling petrographic observations with Qtz-Ab-Or-H2O phase relations, we determined both the amounts of actual melt and the maximum possible amounts of melt in the samples.
Melting efficiency was everywhere less than 100% and decreased with distance from the intrusion. Though perhaps not the only
possible source of fluid throughout the aureole, simple models demonstrate that H2O evolution from the pluton would have been volumetrically sufficient and persisted long enough to account for the observed
partial melting. A time-integrated fluid flux of 7000 kg/m2 from the pluton is necessary to account for the observed amounts of partial melt in the Appin Quartzite. From its inefficiency,
we infer that infiltration of the Appin Quartzite cannot have occurred along interconnected grain-edge channels. Rather, it
was controlled by hydraulic fracturing, with fracture density determining melting efficiency. Bulk-rock permeability is calculated
to be 10−20 m2, an order of magnitude lower than that necessary to permit pervasive flow of all the fluid exsolving from the pluton. There
is little difference between the calculated time-integrated fluid flux through the Appin Quartzite on the eastern flank and
an estimate of the infiltrating flux through the pelitic Leven Schist on the western flank in the time interval during which
both rock types were above their solidus temperature, despite differences in their equilibrium quartz-H2O dihedral angles at temperatures immediately below the solidus, and differences in the attitude of the contact. The rates
of H2O expulsion from the cooling pluton are consistent with highly efficient fracture-dominated flow, allowing insufficient time
for textural equilibration.
Received: 26 March 1998 / Accepted: 8 March 1999 相似文献
12.
The complication introduced by solid solutions in the analysis of infiltration-driven mineral reactions is that the mole fraction of tracer component i in fluid (X i) changes with reaction progress (ξ). The effect was incorporated into transport models for coupled fluid flow and mineral reaction by parameterizing the relation between X i and ξ. With specific reference to carbonation and hydration during regional metamorphism of the peridotite body in Val d’Efra, whose constituent minerals are all solid solutions, infiltration of a disequilibrium fluid produces a single sharp reaction front if rock is assumed uniform in composition. The reaction front separates completely unreacted rock downstream from rock upstream with ξ at a steady-state limit (ξss ≤ ξmax) that depends on input fluid composition (ξmax is the maximum possible value). Novel phenomena develop, however, if the flow medium, like the metaperidotite body, is composed of many small domains that differ in initial mineral modes and compositions but with X i homogenized at a spatial scale larger than the size of the domains (e.g., by diffusion). In this case, infiltration of a disequilibrium fluid produces up to as many different reaction fronts along the flow path as there are domains with 0 ≤ ξ < ξss in all domains except upstream from the slowest moving front where ξ = ξss in all domains. Measured values of ξ in the metaperidotite, (all 0 < ξ < ξmax) are best reproduced by down-temperature infiltration of a disequilibrium fluid with X\textCO2 = 0. 1 9 6 X_{{{\text{CO}}_{2} }} = \, 0. 1 9 6 into a multi-domain medium with uniform X\textCO2 X_{{{\text{CO}}_{2} }} at each spatial point along the flow path (homogenized across the domains at the m-scale by diffusion), and time-integrated fluid flux ≥1,836 mol fluid/cm2 rock. Results resolve the paradox of the widespread spatial distribution of reactants and products of infiltration-driven decarbonation/dehydration reactions in regional metamorphic terrains (which in the absence of solid solution and compositional domains indicate up-temperature flow) and the prediction of hydrodynamic models that regional metamorphic fluid flow normally is directed vertically upward and down temperature. 相似文献
13.
Andreas Tennie Radegund Hoffbauer Stephan Hoernes 《Contributions to Mineralogy and Petrology》1998,133(4):346-355
The oxygen isotope fractionation between kyanite and calcium carbonate has been investigated experimentally at four temperatures
in the range between 625 and 775 °C at 13 kbar. Because of low exchange rates, the isotopic reaction was enhanced by polymorphic
transformation of andalusite to kyanite. With this experimental modification a close approach to equilibrium was reached in
all runs. The temperature dependence of the equilibrium fractionation is described by the equation 1000 ln ky-cc=−2.62×106/T
2. Application of the experimental results to natural quartz-kyanite-garnet assemblages indicates the preservation of the oxygen
isotope composition of kyanite acquired during its formation, reflecting its extremely low oxygen diffusivity. This refractory
behaviour restricts the use of kyanite for thermometry but opens the possibility to use its O-isotope composition as an indicator
for recognition of polymetamorphic rock histories and reconstruction of the prograde evolution of a metamorphic sequence.
Received: 8 June 1998 / Accepted: 24 August 1998 相似文献
14.
V. López Sánchez-Vizcaíno J. A. D. Connolly M. T. Gómez-Pugnaire 《Contributions to Mineralogy and Petrology》1997,126(3):292-302
Phase relations and metamorphic conditions have been studied in metacarbonate rocks from the Nevado-Filábride Complex (Cordilleras
Béticas) through forward modeling. In many rock samples, the assemblage titanite + rutile + calcite + quartz + graphite buffered
the composition of the C-O-H fluid present during metamorphism. Over a wide range of P-T conditions, fluid compositions computed for this buffer are essentially binary H2O-CO2 mixtures. This buffer also constrains the chemical potentials of TiO2, CaO and SiO2. Consequently it is possible to make a thermodynamic projection through these components to predict the stable phase relations
consistent with the buffer. Using this method, phase relations have been analyzed in a rock containing the buffer assemblage
and paragonite, albite, phengite, epidote, and chlorite. The equilibrium P-T conditions for this assemblage are constrained, by minimization of the differences between predicted and observed mineral
compositions, to be 560 ± 15 °C and 9.5 ± 1 kbar. Conditions obtained compare well with those estimated from other studies
in different lithologic units. The inferred metamorphic fluid composition is H2O-rich ().
Received: 11 October 1995 / Accepted 5 August 1996 相似文献
15.
Ian Cartwright Ian S. Buick Roland Maas 《Contributions to Mineralogy and Petrology》1997,128(4):335-351
The Jervois region of the Arunta Inlier, central Australia, contains para- and orthogneisses that underwent low-pressure
amphibolite facies metamorphism (P = 200–300 MPa, T = 520–600 °C). Marble layers cut by metre-wide quartz + garnet ± epidote veins comprise calcite, quartz, epidote, clinopyroxene,
grandite garnet, and locally wollastonite. The marbles also contain locally discordant decimetre-thick garnet and epidote
skarn layers. The mineral assemblages imply that the rocks were infiltrated by water-rich fluids (XCO2 = 0.1–0.3) at ∼600 °C. The fluids were probably derived from the quartz-garnet vein systems that represent conduits for fluids
exsolved from crystallizing pegmatites emplaced close to the metamorphic peak. At one locality, the marble has calcite (Cc)
δ18O values of 9–18‰ and garnet (Gnt) δ18O values of 10–14‰. The δ18O(Gnt) values are only poorly correlated with δ18O(Cc), and the δ18O values of some garnet cores are higher than the rims. The isotopic disequilibrium indicates that garnet grew before the
δ18O values of the rock were reset. The marbles contain ≤15% garnet and, for water-rich fluids, garnet-forming reactions are
predicted to propagate faster than O-isotopes are reset. The Sm-Nd and Pb-Pb ages of garnets imply that fluid flow occurred
at 1750–1720 Ma. There are no significant age differences between garnet cores and rims, suggesting that fluid flow was relatively
rapid. Texturally late epidote has δ18O values of 1.5–6.2‰ implying δ18O(H2O) values of 2–7‰. Waters with such low-δ18O values are probably at least partly meteoric in origin, and the epidote may be recording the late influx of meteoric water
into a cooling hydrothermal system.
Received: 29 April 1996 / Accepted: 12 March 1997 相似文献
16.
B. Cesare 《Contributions to Mineralogy and Petrology》1995,122(1-2):25-33
Equilibrium C–O–H fluid speciation calculations predict that graphite will precipitate from initially graphite saturated
fluid inclusions during cooling and exhumation of metamorphic rocks. In the case that no mass is gained or lost by the inclusions,
the original X
O ratio [O/(O+H)] of the fluid phase must be maintained. Given this closed system constraint, the down-temperature progress
of graphite precipitation can easily be monitored as a function of the varible X
O, and produces some effects that are of significance to fluid inclusion studies: 1. Variation of the H2O : CO2 : CH4 relationship in the graphite-saturated COH fluid, namely increase of X
H2
O and decrease of the carbonic fraction; 2. Decrease of fluid density due to precipitation of graphite, which is denser than
the residual fluid; 3. Alteration of the CO2 : CH4 ratio of the fluid, depending on the initial O : H ratio of the fluid: for X
O>1/3, fluids increase their CO2 : CH4 ratio with decreasing temperature, and vice-versa. This implies that the CO2 : CH4 ratio measured at room T will not represent the trapping value, which is in any case closer to unity. As a consequence of density reduction, isochores
extrapolated from densities observed at room temperature do not pass through the pressure-temperature conditions at which
the inclusion was trapped, with pressure underestimates of up to 2 kbar. Actual P-T trapping conditions are located along the equilibrium “bulk isochore” (curve of constant-X
O, constant-volume) of the fluid. Alteration of the CO2 : CH4 ratio is a mechanism by which a CO2-rich or CH4-rich carbonic phase can be formed from aqueous fluids that are slightly off the neutral X
O=1/3 value. Subsequent segregation of this phase from the aqueous counterpart may account for the formation of pure CO2 and CH4 fluids in the upper crust.
Received: 15 March 1995 / Accepted: 1 June 1995 相似文献
17.
Hydroxyl defects in garnets from mantle xenoliths in kimberlites of the Siberian platform 总被引:12,自引:0,他引:12
A suite of more than 200 garnet single crystals, extracted from 150 xenoliths, covering the whole range of types of garnet
parageneses in mantle xenoliths so far known from kimberlites of the Siberian platform and collected from nearly all the kimberlite
pipes known in that tectonic unit, as well as some garnets found as inclusions in diamonds and olivine megacrysts from such
kimberlites, were studied by means of electron microprobe analysis and single-crystal IR absorption spectroscopy in the v
OH vibrational range in search of the occurrence, energy and intensity of the v
OH bands of hydroxyl defects in such garnets and its potential use in an elucidation of the nature of the fluid phase in the
mantle beneath the Siberian platform. The v
OH single-crystal spectra show either one or a combination of two or more of the following major v
OH bands, I 3645–3662 cm−1, II 3561–3583 cm−1, III 3515–3527 cm−1, and minor bands, Ia 3623–3631 cm−1, IIa 3593–3607 cm−1. The type of combination of such bands in the spectrum of a specific garnet depends on the type of the rock series of the
host xenolith, Mg, Mg-Ca, Ca, Mg-Fe, or alkremite, on the xenolith type as well as on the chemical composition of the respective
garnet. Nearly all garnets contain band systems I and II. Band system III occurs in Ti-rich garnets, with wt% TiO2 > ca. 0.4, from xenoliths of the Mg-Ca and Mg-Fe series, only. The v
OH spectra do not correspond to those of OH− defects in synthetic pyropes or natural ultra-high pressure garnets from diamondiferous metamorphics. There were no indications
of v
OH from inclusions of other minerals within the selected 60 × 60 μm measuring areas in the garnets. The v
OH spectra of pyrope-knorringite- and pyrope-knorringite-uvarovite-rich garnets included in diamonds do not show band systems
I to III. Instead, they exhibit one weak, broad band (Δv
OH 200–460 cm−1) near 3570 cm−1, a result that was also obtained on pyrope-knorringite-rich garnets extracted from two olivine megacrysts. The quantitative
evaluation, on the basis of relevant existing calibrational data (Bell et al. 1995), of the sum of integral intensities of
all v
OH bonds of the garnets studied yielded a wide range of “water” concentrations within the set of the different garnets, between
values below the detection limit of our single-crystal IR method, near 2 × 10−4 wt%, up to 163 × 10−4 wt%. The “water” contents vary in a complex manner in garnets from different xenolith types, obviously depending on a large
number of constraints, inherent in the crystal chemistry as well as the formation conditions of the garnets during the crystallization
of their mantle host rocks. Secondary alteration effects during uplift of the kimberlite, play, if any, only a minor role.
Despite the very complex pattern of the “water” contents of the garnets, preventing an evaluation of a straightforward correlation
between “water” contents of the garnets and the composition of the mantle's fluid phase during garnet formation, at least
two general conclusions could be drawn: (1) the wide variation of “water” contents in garnets is not indicative of regional
or local differences in the composition of the mantle's fluid phase; (2) garnets formed in the high-pressure/high-temperature
diamond-pyrope facies invariably contain significantly lower amounts of “water” than garnets formed under the conditions of
the graphite-pyrope facies. This latter result (2) may point to significantly lower f
H2O and f
O2 in the former as compared to the latter facies.
Received: 25 November 1997 / Accepted: 9 March 1998 相似文献
18.
J. L. Mosenfelder 《Physics and Chemistry of Minerals》2000,27(9):610-617
The solubility of hydroxyl in coesite was investigated in multianvil experiments performed at 1200 °C over the nominal pressure
range 5–10 GPa, at an f
O2 close to the Ni-NiO buffer. The starting material for each experiment was a cylinder of pure silica glass plus talc, which
dehydrates at high P and T to provide a source of water and hydrogen (plus enstatite and excess SiO2). Fourier-transform infrared (FTIR) spectra of the recovered coesite crystals show five sharp bands at 3606, 3573, 3523,
3459, and 3299 cm−1, indicative of structurally bonded hydrogen (hydroxyl). The concentration of hydrogen increases with pressure from 285 H/106 Si (at 5 GPa) to 1415 H/106 Si (at 10 GPa). Assuming a model of incorporation by (4H)Si defects, the data are fit well by the equation C
OH=Af
2
H2<\INF>Oexp(−PΔV/RT), with A=4.38 H/106 Si/GPa, and ΔV=20.6 × 10−6 m3 mol−1. An alternative model entailing association of hydrogen with cation substitution can also be used to fit the data. These
results show that the solubility of hydroxyl in coesite is approximately an order of magnitude lower than in olivines and
pyroxenes, but comparable to that in pyropic garnet. However, FTIR investigations on a variety of ultrahigh pressure metamorphic
rocks have failed in all cases to detect the presence of water or hydrogen in coesite, indicating either that it grew in dry
environments or lost its hydrogen during partial transformation to quartz. On the other hand, micro-FTIR investigations of
quartz crystals replacing coesite show that they contain varying amounts of H2O. These results support the hypothesis that preservation of coesite is not necessarily linked to fast exhumation rates but
is crucially dependent on limited fluid infiltration during exhumation.
Received: 23 August 1999 / Accepted: 10 April 2000 相似文献
19.
Meta-sedimentary rocks including marbles and calcsilicates in Central Dronning Maud Land (CDML) in East Antarctica experienced
a Pan-African granulite facies metamorphism with peak metamorphic conditions around 830 ± 20 °C at 6.8 ± 0.5 kbar which was
accompanied by the post-kinematic intrusion of huge amounts of syenitic (charnockitic) magmas at 4.5 ± 0.7 kbar. The marbles
and calcsilicates may represent meta-evaporites as indicated by the occurrence of metamorphic gypsum/anhydrite and Cl-rich
scapolite that formed in the presence of saline fluids with X
NaCl in the range 0.15–0.27. The marbles and calcsilicates bear biotite, tremolite and/or hornblende and humite group minerals
(clinohumite, chondrodite and humite) which are inferred to have crystallized at about 650 °C and 4.5 kbar. The syenitic intrusives
contain late-magmatic biotite and amphibole (formed between 750 and 800 °C) as well as relictic magmatic fayalite, orthopyroxene
and clinopyroxene. Two syenite and two calcsilicate samples contain fluorite. Corona textures in the marbles and calcsilicates
suggest very low fluid-rock ratios during the formation of the retrograde (650 °C) assemblages. Biotite in all but two syenite
samples crystallized at log(f
H
2
O/f
HF) ratios of 2.9 ± 0.4, while in the calcsilicates, both biotite and humite group minerals indicate generally higher log(f
H
2
O/f
HF) values of up to 5.2. A few samples, though, overlap with the syenite values. Log(f
H
2
O/f
HCl) derived from biotite covers the range 0.5–2.6 in all rock types. Within a single sample, the calculated values for both
parameters vary typically by 0.1 to 0.8 log units. Water and halogen acid fugacities calculated from biotite-olivine/orthopyroxene-feldspar-quartz
equilibria and the above fugacity ratios are 1510–2790 bars for H2O, 1.3–5.3 bars for HF and 7–600 bars for HCl. The results are interpreted to reflect the reaction of relatively homogeneous
magmatic fluids [in terms of log(f
H
2
O
/f
HF)] derived from the late-magmatic stages of the syenites with both earlier crystallized, still hotter parts of the syenites
and with adjacent country rocks during down-temperature fluid flow. Fluorine is successively removed from the fluid and incorporated
into F-bearing minerals (close to the syenite into metamorphic fluorite). In the course of this process log(f
H
2
O
/f
HF) increases significantly. Chlorine preferably partitions into the fluid and hence log(f
H
2
O
/f
HCl) does not change markedly during fluid-rock interaction.
Received: 28 November 1997 / Accepted: 27 April 1998 相似文献
20.
Jean-Claude Vannay Zachary D. Sharp Bernhard Grasemann 《Contributions to Mineralogy and Petrology》1999,137(1-2):90-101
Inverted metamorphic field gradients are preserved in two amphibolite facies metapelitic sequences forming the crystalline
core zone of the Himalayan orogen in the Sutlej valley (NW India). In the High Himalayan Crystalline Sequence (HHCS), metamorphic
conditions increase upwards from the staurolite zone at the base, through the kyanite-in and sillimanite-in isograds, finally
to reach partial melting conditions at the top. The structurally lower Lesser Himalayan Crystalline Sequence (LHCS) shows
a gradual superposition of garnet-in, staurolite-in and kyanite + sillimanite-in isograds. Although phase equilibria constraints
imply inverted temperature field gradients in both units, garnet-biotite (GARB) rim thermometry indicates final equilibration
at a nearly uniform temperature around T ≈ 600 °C across these sequences. The P-T path and garnet zoning data show that this apparent lack of thermal field gradient is mainly the consequence of a resetting
of the GARB equilibria during cooling. In order to constrain peak temperature conditions, 20 samples along the studied section
have been analysed for oxygen isotope thermometry. The isotopic fractionations recorded by quartz-garnet and quartz-aluminosilicate
mineral pairs indicate temperatures consistent with phase equilibria and P-T path constraints for metamorphic peak conditions. Together with barometry results, based on net transfer continuous reactions,
the oxygen isotope thermometry indicates peak conditions characterized by: (1) a temperature increase from T ≈ 570 to 750 °C at a nearly constant pressure around P ≈ 800 MPa, from the base to the top of the HHCS unit; (2) a temperature increase from T ≈ 610 to 700 °C and a pressure decrease from P ≈ 900 to 700 MPa, from the base to the top of the LHCS metapelites. Oxygen isotope thermometry thus provides the first quantitative
data demonstrating that the Himalayan inverted metamorphism can be associated with a complete inversion of the thermal field
gradient across the crystalline core zone of this orogen.
Received: 1 April 1999 / Accepted: 12 July 1999 相似文献