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1.
Formation of Wollastonite by Chemically Reactive Fluid Flow During Contact Metamorphism, Mt. Morrison Pendant, Sierra Nevada, California, USA 总被引：2，自引：1，他引：2
Quartz–calcite sandstones experienced the reaction calcite+ quartz = wollastonite + CO2 during prograde contact metamorphismat P = 1500 bars and T = 560°C. Rocks were in equilibriumduring reaction with a CO2–H2O fluid with XCO2 = 0·14.The transition from calcite-bearing, wollastonite-free to wollastonite-bearing,calcite-free rocks across the wollastonite isograd is only severalmillimeters wide. The wollastonite-forming reaction was drivenby infiltration of quartz–calcite sandstone by chemicallyreactive H2O-rich fluids, and the distribution of wollastonitedirectly images the flow paths of reactive fluids during metamorphism.The mapped distribution of wollastonite and modeling of an O-isotopeprofile across a lithologic contact indicate that the principaldirection of flow was layer-parallel, directed upward, withany cross-layer component of flow <0·1% of the layer-parallelcomponent. Fluid flow was channeled at a scale of 1–100m by pre-metamorphic dikes, thrust and strike-slip faults, foldhinges, bedding, and stratigraphic contacts. Limits on the amountof fluid, based on minimum and maximum estimates for the displacementof the wollastonite reaction front from the fluid source, are(0·7–1·9) x 105 cm3 fluid/cm2 rock. Thesharpness of the wollastonite isograd, the consistency of mineralthermobarometry, the uniform measured 18O–16O fractionationsbetween quartz and calcite, and model calculations all arguefor a close approach to local mineral–fluid equilibriumduring the wollastonite-forming reaction. KEY WORDS: contact metamorphism, fluid flow, wollastonite, oxygen isotopes, reaction front 相似文献
2.
The Stability of Andradite, Hedenbergite, and Related Minerals in the System Ca--Fe--Si--O--H 总被引：3，自引：0，他引：3
Phase relations for the bulk compositions 3CaO·2FeOx·3SiO2+excessH2O and CaO·FeOx·2SiO2+excess H2O were determinedusing conventional hydrothermal techniques with solid phaseoxygen buffers to control fO2. Andradite, Ca3Fe3+2Si3O12, synthesized above 550 °C hasan average unit cell edge, ao, of 12.055±0.001 Å,and an index of refraction, n, of 1.887±0.003. Belowthis temperature, ao increases whereas n decreases, indicatingthe formation of a member of the andradite-hydroandradite solidsolution. At 2000 bars Pfluid andradite is stable above an fO2of 1015 bar at 800 °C and 10-32 bar at 400 °C. At lowerfO2 andradite+fluid gives way at successively lower temperaturesto the condensed assemblages magnetite+wollastonite, kirschsteinite(CaFe2+SiO4)+ wollastonite and kirschsteinite+xonotlite (Ca6Si6O17(OH)2). Synthetic hedenbergite, CaFe2+Si2O6, has average unit cell dimensionsof ao = 9.857± 0.004 Å, bo = 9.033±0.002Å, co = 5.254±0.002 Å and ß = 104.82°±0.03°,and refractive indices of n = 1.731±0.003 and n = 1.755±0.005.At 2000 bars Pfiuid, hedenbergite is stable below an fO2 of10-13 bar at 800 °C and 10-28 bar at 400 °C. Above thesefO2 values, hedenbergite+O2 breaks down to andradite+magnetite+quartz. The mineral pair andradite +hedenbergite thus limit the fO2range possible for their joint formation under equilibrium conditions. The hydration of wollastonite to xonotlite occurs at much lowertemperatures than previous experimental work indicated. A tentativehigh temperature limit for this reaction is set at 185°±15°C and 5000±25 bars and 210°±15 °Cand 2000±20 bars. Inasmuch as the growth of xonotlitefrom wollastonite + H2O was never accomplished, this high temperaturelimit does not represent an equilibrium univariant curve. Nine phases were encountered in the study of andradite and hedenbergite.They are andradite, hedenbergite, magnetite, wollastonite, kirschsteinite,xonotlite, quartz, ilvaite, and vapor (fluid). An invariantpoint analysis using the method of Schreinemakers shows thetopologic relations of the reactions involved. The resultinggrid can be used to interpret natural occurrences. 相似文献
3.
The biotite isograd in pelitic schists of the Waterville Formationinvolved reaction of muscovite + ankerite + rutile + pyrite+graphite + siderite or calcite to form biotite + plagioclase+ ilmenite. There was no single reaction in all pelites; eachrock experienced a unique reaction depending on the mineralogyand proportions of minerals in the chlorite-zone equivalentfrom which it evolved. Quartz, chlorite, and pyrrhotite werereactants in some rocks and products in others. All inferredbiotite-forming reactions involved decarbonation and desulfidation;some were dehydration reactions and others were hydration reactions.P-T conditions at the biotite isograd were near 3500 bars and400 °C. C-O-H-S fluids in equilibrium with the pelitic rockswere close to binary CO2-H2O mixtures with XCO2 = 0.02–0.04.During the biotite-forming reaction, pelitic rocks (a) decreasedby 2–5 percent in volume, (b) performed – (4–11)kcal/liter P-V work on their surroundings, (c) absorbed 38–85kcal/liter heat from their surroundings, and (d) were infiltratedby at least 0.9–2.2 rock volumes H2O fluid. The biotite isograd sharply marks the limit of a decarbonationfront that passed through the terrane during regional metamorphism.Decarbonation converted meta-shales with 6–10 per centcarbonate to carbonate-free pelitic schists. One essential causeof the decarbonation event was pervasive infiltration of theterrane by at least 1–2 rock volumes H2O fluid early inthe metamorphic event under P-T conditions of the biotite isograd.Average shale contains 4–13 per cent siderite, ankerite,and/or calcite, but average pelitic schist is devoid of carbonateminerals. If the Waterville Formation serves as a general modelfor the metamorphism of pelitic rocks, it is likely that worldwidemany pelitic schists developed by decarbonation of shale caused,in part, by pervasive infiltration of metamorphic terranes byseveral rock volumes of aqueous fluid during an early stageof the metamorphic event. 相似文献
4.
Metamorphism and Structure of Penfold Creek Area, near Quesnel Lake, British Columbia 总被引：1，自引：0，他引：1
The Quesnel Lake area lies within the Omineca Crystalline Belt,and is underlain by the northern extremity of the Shuswap MetamorphicComplex. Closely spaced and steeply dipping isograds mark themargins of the metamorphic belt. In the Penfold Creek area onlyone and one-half miles separate the biotite and sillimaniteisograds. Related to this sharp increase in metamorphic gradethere is a marked change in the fold style. In the chloritezone are similar folds, showing a strong axial-plane cleavage,and tight refolded isoclines dominate in the sillimanite zone.Three periods of deformation and two periods of prograde metamorphismhave been recognized, with the first metamorphic period beingassociated with Phase 2 deformation and the second being post-Phase2. Regression analysis of possible mineral reactions in these rocksshows that they formed under conditions of a gradient in temperatureand possibly H2O activity, and that most of the assemblages,although containing many phases, have at least two degrees offreedom. Thermodynamic analysis of mineral equilibria indicatesthat equilibrium was closely approached between solid solutionsinvolving garnet, plagioclase, biotite, white mica, and staurolitein the presence of Al2SiO5, quartz, and H2O. The conditionsof metamorphism of rocks containing Al2SiO5 are estimated tobe 7000 ± 1500 bars, 680 ± 30 °C, activityof H2O = 0.80 (approx.). Partial melting did not occur becauseof the reduced activity of H2O.
*Present address: Overseas Division, Institute of Geological Sciences, 5 Princes Gate, London SW7, England. 相似文献
5.
Certain ultramafic-mafic lenses exposed in Ticino along thecontact zone between the underlying Simano and overlying Adulanappes display relatively high-pressure phase assemblages. AtAlpe Arami, metabasaltic layers associated with pyropic garnet-bearingIherzolite consist mainly of an early eclogitic assemblage characterizedby Alm39Py37Gross23Spess01+ Di49Hd08Jd43+rutile±kyanite.Iron-magnesium fractionation between garnet+omphacite pairsyields a KD, (Fe2+/Mg)garnet/(Fe2+/Mg)cllnopyroxence, of about6. This earlier assemblage has been replaced by a later, somewhatpargasitic hornblende+oligoclase+clinozoisite phase compatibility.Associated primary garnet peridotites contain Ca-rich clinopyroxeneand Al2O3-poor orthopyroxene. Both rock types have been affectedby a still later period of incipient chloritization. Available phase equilibrium and element partitioning data arecompatible with an inferred P-T condition of origin for theAlpe Arami mafic-ultramafic complex of 965–1000 °C,30–50 kilobars, indicating deep upper mantle generation.Amphibolites could have been produced during depressurizationaccompanying ascent of the mass through the upper mantle, butinasmuch as plagioclase accompanies the hornblende, the assemblageprobably crystallized after emplacement of the complex in theLepontine terrane prior to the termination of the Late Alpineregional metamorphism. Incipient production of high-rank greenschistphases certainly reflects a crustal event. 相似文献
6.
Contact-mctamorphic assemblages in ophicarbonate from the Bergellaureole correspond either to model isobaric invariant T-XCO2points [Atg-Cal-Di-Tr-Fo (6 samples) and Atg-Cal-Tr-Fo-Dol (2)]or to isobaric univariant T-XCO2, curves [Tr-Cal-Di-Atg (18),Tr-Dol-Atg-Cal (1), Atg-Cal-Fo-Di (1), and Atg-Cal-Tr-Fo (1)].Calcite-dolomite thermometry and mineral-fluid equilibria inthe invariant assemblages record T=440–540C at P=3•5kbar. Equilibrium metamorphic fluids were very H2O rich withX CO2,=0•001–0•027. In the invariant assemblagesTr + Fo were produced by prograde decarbonation-dehydrationreactions. In contrast, measured modes and reaction texturesin samples with univariant assemblages indicate thai Tr wasproduced by carbonation reactions. The apparent paradox of simultaneousdecarbonation reactions in the model isobaric invariant assemblagesand carbonation reactions in univariant assemblages is resolvedby local mineral-fluid equilibrium and fluid flow through ophicarbohatesin the direction of decreasing temperature as the aureole heated.Time-integrated flux (q) was computed from measured reactionprogress in 28 samples for models of both horizontal and verticaldown-temperature flow. Results are similar, with q decreasingrapidly from (0•2–5•1) 105 cm3 fluid/cm2 rock1•3–1•7 km from the intrusion to 0–0•6105cm3/cm2 at 1•8–4•0 km. The decrease in q ismore consistent with vertical than horizontal flow. Variationsin time-integrated flux of more than an order of magnitude arerecorded by samples from the same outcrop. The absence of carbonatein adjacent metaperidotite indicates that flow was confinedto the ophicarbonate. Channelized, spatially heterogeneous,vertical flow can be explained by the brecciation and strongvertical foliation of the ophicarbonate relative to surroundingmassive metaperidotite. Generation of metamorphicfluids by decarbonation-dehydrationreactions within the ophicarbonates explains larger averageflux 1–2 km from the intrusion compared with more distalpoints. KEY WORDS: Bergell; contact metamorphism; fluid flow; ophicarbonate
*Telephone: (410) 516-8121. Fax: (410) 516-7933 相似文献
7.
Al2SiO5 reaction textures in aluminous schist and quartziteof the northern Picuris range, north-central New Mexico, recorda paragenetic sequence of kyanite to sillimanite to andalusite,consistent with a clockwise P–T loop, with minor decompressionnear the Al2SiO5 triple-point. Peak metamorphic temperaturesare estimated at 510–525°C, at 4·0–4·2kbar. Kyanite and fibrolite are strongly deformed; some prismaticsillimanite, and all andalusite are relatively undeformed. Monaziteoccurs as inclusions within kyanite, mats of sillimanite andcentimetre-scale porphyroblasts of andalusite, and is typicallyaligned subparallel to the dominant regional foliation (S0/S1or S2) and extension lineation (L1). Back-scatter electron imagesand X-ray maps of monazite reveal distinct core, intermediateand rim compositional domains. Monazite–xenotime thermometryfrom the intermediate and rim domains yields temperatures of405–470°C (±50°C) and 500–520°C(±50°C), respectively, consistent with the progradeto peak metamorphic growth of monazite. In situ, ion microprobeanalyses from five monazites yield an upper intercept age of1417 ± 9 Ma. Near-concordant to concordant analyses yield207Pb–206Pb ages from 1434 ± 12 Ma (core) to 1390± 20 Ma (rim). We find no evidence of older regionalmetamorphism related to the 1650 Ma Mazatzal Orogeny. KEY WORDS: Al2SiO5; metamorphism; monazite; thermochronometry; triple-point 相似文献
8.
Frezzotti Maria Luce; Ferrando Simona; Dallai Luigi; Compagnoni Roberto 《Journal of Petrology》2007,48(6):1219-1241
Minerals, fluid inclusions and stable isotopes have been studiedin ultrahigh-pressure (UHP) OH-rich topaz–kyanite quartzitesfrom Hushan (west of Dongai), in southern Sulu (China). Thequartzites underwent a metamorphic evolution characterized bya peak stage (3·5 GPa and 730–820°C) with theanhydrous assemblage coesite + kyanite I, followed by an earlynear-isothermal decompression stage (2·9 GPa and 705–780°C)with growth of kyanite II, muscovite, and OH-rich topaz, andby decompression-cooling stages, represented by paragonite (1·9GPa and 700–780°C) and pyrophyllite (0·3 GPaand 400°C) on kyanite (I and II) and OH-rich topaz, respectively.These rocks may exhibit unusually low 18O and D values acquiredbefore undergoing UHP metamorphism. Five distinct fluid generationsare recognized. Type I: concentrated peak solutions rich inSi, Al, and alkalis, present within multiphase inclusions inkyanite I. Type II: CaCl2-rich brines present during the growthof early retrograde OH-rich topaz. Type III, IV, and V: lateaqueous fluids of variable salinity, and rare CO2 present duringamphibolite- and late greenschist-facies conditions. A numberof conclusions may be drawn from these relationships that havean effect on fluid evolution in deeply subducted continentalrocks. (1) At a pressure of about 3·5 GPa alkali–alumino-silicateaqueous solutions, with compositions intermediate between H2Ofluid and melt (H2O > 25 and 50 wt %) evolved from quartzites,probably generated by dehydration reactions. (2) During earlydecompression stages, at the transition from UHP to high-pressure(2·9 GPa) conditions, brines of external origin withhigher water contents (82 wt % H2O) initiated the growth ofOH-rich topaz and muscovite. (3) The subsequent decompression,at P <2 GPa, was defined by a limited circulation of NaClaqueous fluids, and CO2 infiltration. Overall, fluid inclusionsand stable isotopes highlight a metamorphic fluid–rockinteraction characterized by internally derived intermediateaqueous solutions at UHP, followed by infiltration of Cl-richbrines with higher water activities. KEY WORDS: ultrahigh-pressure metamorphism; OH-rich topaz; fluid inclusions; stable isotopes; supercritical liquids 相似文献
9.
K-feldspar–plagioclase–quartz mineral textures aswell as biotite and hornblende compositions are compared forsuites of metamorphosed mafic rocks from two widely separatedtraverses. A portion of either traverse has experienced a high-gradedehydration event transforming it from an H2O-rich, hornblende-bearingzone to an H2O-poor, hornblende-free, orthopyroxene-bearing,‘granulite facies’ zone at 700–800°C and7–8 kbar. In the Kigluaik Mountains, Seward Peninsula,Alaska, dehydration took place over an 85 cm thick layer ofmetatonalite in contact with a marble during regional metamorphismand involved a CO2-rich fluid, whereas for the Val Strona diOmegna traverse, Ivrea–Verbano Zone, northern Italy, dehydrationtook place over a 3–4 km thick sequence of metabasitesinterlayered with metapelites in a contact metamorphic eventinvolving basaltic magmas intruded at the base of the sequence.Orthopyroxene-bearing samples from both dehydration zones showmicro-veins of K-feldspar along quartz and plagioclase grainboundaries as well as replacement antiperthite in plagioclase.K came primarily from the breakdown of hornblende + quartz toorthopyroxene ± clinopyroxene, feldspar and fluid. Biotiteeither was stabilized or formed in the dehydration zones andis enriched in Ti, Mg, F and Cl relative to biotite in the amphibolitefacies zone. KEY WORDS: KCl–NaCl brines; metasomatism; granulite facies metamorphism; charnockite–enderbite; orthopyroxene; K-feldspar; biotite; hornblende 相似文献
10.
The terrane in the Panamint Mountains, California, was regionallymetamorphosed under low-pressure conditions and subsequentlyunderwent retrograde metamorphism. Prograde metamorphic isogradsthat mark the stability of tremolite + calcite, diopside, andsillimanite indicate a westward increase in grade. The studywas undertaken to determine the effects of the addition of Caon the types of assemblages that may occur in pelitic schists,to contribute to the understanding of the stability limits inP – T – aH2O – XFe of the pelitic assemblagechlorite + muscovite + quartz, and to estimate the change inenvironment from prograde to retrograde metamorphism. Peliticassemblages are characterized by andalusite + biotite + stauroliteand andalusite + biotite + cordierite. Within a small changein grade, chlorite breaks down over nearly the entire rangein Mg/(Mg + Fe) to biotite + aluminous mineral. Chlorite withMg/(Mg + Fe) = 0.55 is stable to the highest grade, and thegeneralized terminal reaction is chlorite + muscovite + quartz= andalusite + biotite + cordierite + H2O. Calcic schists arecharacterized by the assemblage epidote + muscovite + quartz+ chlorite + actinolite + biotite + calcite + plagioclase atlow grades and by epidote + muscovite + quartz + garnet + hornblende+ biotite + calcite + plagioclase at high grades. Epidote doesnot coexist with any AFM phase that is more aluminous than garnetor chlorite. Lithostatic pressure ranged from 2.3 kb to 3.0kb. During prograde-metamorphism temperatures ranged from lessthan 400° to nearly 700°C, and XH2O (assuming PH2O +PCO3 = Ptotal) is estimated to be 0.25 in siliceous dolomite,0.8 in pelitic schist, and 1.0 in calcic schist. Temperatureduring retrograde metamorphism was 450° ± 50°C,and all fluid were H2O-rich. A flux of H2O-rich fluid duringfolding is believed to have caused retrograde metamorphism.The petrogenetic grid of Albee (1965b) is modified to positionthe (A, Cd) invariant point relative to the aluminosilicatetriple point, which allows the comparison of facies series thatinvolve different chloritoid-reactions. 相似文献
11.
Granulite-facies quartzofeldpathic gneisses metamorphosed 1000m.y. ago are exposed around Molodezhnaya Station (67°40'S,46°E) in East Antarctica. In addition to quartz, K-feldspar,and plagioclase, the fourteen samples studied in detail consistof the assemblages biotite-orthopyroxene-magnetite, biotite-garnet-orthopyroxene-ilmenite±magnetite, biotite-garnet ± ilmenite ± magnetite,biotite-garnet-sillimanite-ilmenite ± rutile, and biotite-garnet-cordierite-ilmenite-(sillimanite-rutile).Garnets are pyrope-almandine (13 to 34 mol per cent pyrope).Biotite (XFe = 0.33 to 0.57) is rich in TiO2 (4 to 6.3 wt percent) and its Al2O3 content depends on the mineral assemblage.Orthopyroxene (XFe = 0.45 to 0.60) contains 1.5 to 3.0 weightper cent Al2O3. By and large, the minerals are chemically homogeneousand compositional variations are systematic, which indicatecrystallization under equilibrium conditions. On the basis ofthe compositions of coexisting garnet-biotite, garnet-cordierite,garnet-plagioclase (with sillimanite), and garnet-plagioclase-orthopyroxene,temperatures and pressures during the granulite-facies metamorphismare estimated to be 700°C ± 30°C and 5.5 ±1 kb. Water pressure apparently was significantly less thantotal pressure. Alteration during events following the granulite-facies metamorphismhas resulted in chemical zoning in garnet, in which grain edgesare more iron-rich than cores, heterogeneous biotite compositions,and anomalous trends involving MnO. Temperatures based on biotiteand garnet-edge compositions range from 410 to 580°C. Differences in the chemical potential (µ) of water andoxygen in the fluid phase can explain compositional variationsamong the three sillimanite-bearing samples and the relativelyiron-rich compositions of garnet and biotite associated withcordierite. Apparently, the water released by the formationof cordierite remained in the rock, forcing µH2O to increaseas cordierite formed. Buffering of fluid phase composition bythe mineral assemblage suggests that water was not removed fromthe Molodezhnaya rocks by flushing with CO2-rich fluids duringmetamorphism, a hypothesis evoked to explain ‘dry’mineral assemblages in other granulite-facies terrains. 相似文献
12.
Phase Equilibria of Amphibolites from the Post Pond Volcanics, Mt. Cube Quadrangle, Vermont 总被引：1，自引：0，他引：1
Amphibolites of the Post Pond Volcanics, south-west corner ofthe Mt. Cube Quadrangle, Vermont, are characterized by a greatdiversity of bulk rock types that give rise to a wide varietyof low-variance mineral assemblges. Original rock types arebelieved to have been intrusive and extrusive volcanics, hydrothermallyaltered volcanics and volcanogenic sediments with or withoutadmixtures of sedimentary detritus. Metamorphism was of staurolite-kyanitegrade. Geothermometry yields a temperature of 535 ± 20°C at pressures of 5–6 kb. Partitioning of Fe and Mg between coexisting phases is systematic,indicating a close approach to chemical equilibrium was attained.Relative enrichment of Fe/Mg is garnet > staurolite >gedrite > anthophyllite cummingtonite hornblende > biotite> chlorite > wonesite > cordierite dolomite > talc;relative enrichment in Mn/Mg is garnet > dolomite > gedrite> staurolite cummingtonite > hornblende > anthophyllite> cordierite > biotite > wonesite > chlorite >talc. between coexisting amphiboles varies as a function ofbulk Fe/Mg, which is inconsistent with an ideal molecular solutionmodel for amphiboles. Mineral assemblages are conveniently divided into carbonate+ hornblende-bearing, hornblende-bearing (carbonate-absent)and hornblende-absent. The carbonate-bearing assemblages allcontain hornblende + dolomite+ calcite + plagioclase (andesineand/or anorthite) + quartz with the additional phases garnetand epidote (in Fe-rich rocks) and chlorite ± cummingtonite(in magnesian rocks). Carbonate-bearing assemblages are restrictedto the most calcic bulk compositions. Hornblende-bearing (carbonate absent) assemblages occur in rocksof lower CaO content than the carbonate-bearing assemblages.All of these assemblages contain hornblende + andesine ±quartz + Fe-Ti oxide (rutile in magnesian rocks and ilmenitein Fe-rich rocks). In rocks of low Al content, cummingtoniteand two orthoamphiboles (gedrite and anthophyllite) are common.In addition, garnet is found in Fe-rich rocks and chlorite isfound in Mg-rich rocks. Several samples were found that containhornblende + cummingtonite + gedrite + anthophyllite ±garnet +chlorite + andesine + quartz + Fe-Ti oxide ±biotite. Aluminous assemblages contain hornblende + staurolite+ garnet ± anorthite/bytownite (coexisting with andesine)± gedrite ± biotite ± chlorite ±andesine ± quartz ± ilmenite. Hornblende-absentassemblages are restricted to Mg-rich, Ca-poor bulk compositions.These rocks contain chlorite ± cordierite ± staurolite± talc ± gedrite ± anthophyllite ±cummingtonite ± garnet ± biotite ± rutile± quartz ± andesine. The actual assemblage observeddepends strongly on Fe/Mg, Ca/Na and Al/Al + Fe + Mg. The chemistry of these rocks can be represented, to a firstapproximation, by the model system SiO2–Al2O3–MgO–FeO–CaO–Na2O–H2O–CO2;graphical representation is thus achieved by projection fromquartz, andesine, H2O and CO2 into the tetrahedron Fe–Ca–Mg–Al.The volumes defined by compositions of coexisting phases filla large portion of this tetrahedron. In general, the distributionof these phase volumes is quite regular, although in detailthere are a large number of phase volumes that overlap otherphase volumes, especially with respect to Fe/Mg ratios. Algebraicand graphical analysis of numerous different assemblages indicatethat every one of the phase volumes should shift to more magnesiancompositions with decreasing µH2O. It is therefore suggestedthat the overlapping phase volumes are the result of differentassemblages having crystallized in equilibrium with differentvalues of µH2O or µCO2 and that the different valuesmay have been inherited from the original H2O and CO2 contentof the volcanic prototype. If true, this implies that eithera fluid phase was not present during metamorphism, or that fluidflow between rocks was very restricted. 相似文献
13.
An Experimental Study of Water and Carbon Dioxide Solubilities in Mid-Ocean Ridge Basaltic Liquids. Part I: Calibration and Solubility Models 总被引：14，自引：7，他引：7
DIXON JACQUELINE EABY; STOLPER EDWARD M.; HOLLOWAY JOHN R. 《Journal of Petrology》1995,36(6):1607-1631
Experiments were conducted to determine the solubilities ofH2O and CO2 and the nature of their mixing behavior in basalticliquid at pressures and temperature relevant to seqfloor eruption.Mid-ocean ridge basaltic (MORB) liquid was equilibrated at 1200°Cwith pure H2O at pressures of 176–717 bar and H2O—CO2vapor at pressures up to 980 bar. Concentrations and speciationof H2O and CO2 dissolved in the quenched glasses were measuredusing IR spectroscopy. Molar absorptivities for the 4500 cm–1band of hydroxyl groups and the 5200 and 1630 cm–1 bandsof molecular water are 0•67±0•03, 0•62±0•07,and 25±3 l/mol-cm, respectively. These and previouslydetermined molar absorptivities for a range of silicate meltcompositions correlate positively and linearly with the concentrationof tetrahedral cations (Si+Al). The speciation of water in glass quenched from vapor-saturatedbasaltic melt is similar to that determined by Silver &Stolper (Journal of Petrology 30, 667–709, 1989) in albiticglass and can be fitted by their regular ternary solution modelusing the coefficients for albitic glasses. Concentrations ofmolecular water measured in the quenched basaltic glasses areproportional to f H2O in all samples regardless of the compositionof the vapor, demonstrating that the activity of molecular waterin basaltic melts follows Henry's law at these pressures. Abest fit to our data and existing higher-pressure water solubilitydata (Khitarov et al., Geochemistry 5, 479–492, 1959;Hamilton et al., Journal of Petrology 5, 21–39, 1964),assuming Henrian behavior for molecular water and that the dependenceof molecular water content on total water content can be describedby the regular solution model, gives estimates for the Vo, mH2Oof 12±1 cm3/mol and for the 1-bar water solubility of0•11 wt%. Concentrations of CO2 dissolved as carbonate in the melt forpure CO2-saturated and mixed H2O-CO2-saturated experiments area simple function of fCO2 These results suggest Henrian behaviorfor the activity of carbonate in basaltic melt and do not supportthe widely held view that water significantly enhances the solutionof carbon dioxide in basaltic melts. Using a Vo, mr of 23 cm3/mol(Pan et al., Geochimica et Cosmochimica Acta 55, 1587–1595,1991), the solubility of carbonate in the melt at 1 bar and1200°C is 0•5 p.p.m. Our revised determination of CO2solubility is 20% higher than that reported by Stolper &Holloway (Earth and Planetary Science Letters 87, 397–408,1988). KEY WORDS: mid-ocean ridge basalts; water and carbon dioxide solubility; experimental petrology 相似文献
14.
ENCARNACIoN J. P.; ESSENE E. J.; MUKASA S. B.; HALL C. H. 《Journal of Petrology》1995,36(6):1481-1503
Metamorphic rocks exposed near the base of a pre-middle Eoceneophiolite in central Palawan, Philippines, preserve a recordof the P-T-t conditions under which the ophiolite was detachedand emplaced onto the rifted southeast margin of China. Garnetamphibolites in contact with mantle harzburgite preserve peakmetamorphic temperatures of 700–760°C and minimumpressures of 9 kbar, consistent with the presence of kyanite.Garnet grains which preserve strong prograde zoning (Pyp11 incores to Pyp43 in rims) contain inclusion assemblages that constrainpressures above 5–6 kbar at 4O0–500°C. Thisrepresents an early prograde clockwise path consistent withunderthrusting. Two amphibolite samples yield hornblende 39Ar/40Ar–36Ar/Ar40Arisochron ages of 34•0±0•6 Ma (2) (early Oligocene),which are indistinguishable from a 34•3±0•2Ma isochron age of muscovite from a kyanitechlorite-muscoviteschist that is interlayered with the amphibolites. The highpressures (equivalent to a depth of >30 km in oceanic lithosphere)and temperatures, and the age difference between ophiolite crystallizationand metamorphism of the sole, are incompatible with the rockshaving formed in a mature subduction zone or oceanic spreadingcenter. Instead, the timing, P-T conditions, and regional geologysuggest metamorphism in a nascent subduction zone. Rapid coolingand exhumation of the metamorphic rocks followed peak metamorphicconditions in the earliest Oligocene, perhaps by the rapid thickeningof the accretionary complex that is preserved beneath the ophiolite.The amphibolites formed during the inception of southward subductionwithin proto-South China Sea oceanic lithosphere south of theEurasian margin. This led to the formation of an arc-trenchsystem that accommodated extension along southeast China andthe opening of the South China Sea. KEY WORDS: ophiolite; thermobarometry; garnet amphibolite; subduction 相似文献
15.
KADIK A.; PINEAU F.; LITVIN Y.; JENDRZEJEWSKI N.; MARTINEZ I.; JAVOY M. 《Journal of Petrology》2004,45(7):1297-1310
Studies of iron-bearing silicate melt (ferrobasalt) + iron metallicphase + graphite + hydrogen equilibria show that carbon andhydrogen solubilities in melts are important for the evolutionof the upper mantle. In a series of experiments conducted at3·7 GPa and 1520–1600°C, we have characterizedthe nature (oxidized vs reduced) and quantified the abundancesof C- and H-compounds dissolved in iron-bearing silicate melts.Experiments were carried out in an anvil-with-hole apparatuspermitting the achievement of equal chemical potentials of H2in the inner Pt capsule and outer furnace assembly. The fO2for silicate melt–iron equilibrium was 2·32 ±0·04 log units below iron–wüstite (IW). Theferrobasalt used as starting material experienced a reductionof its iron oxides and silicate network. The counterpart wasa liberation of oxygen reacting with the hydrogen entering thecapsule. The amount of H2O dissolved in the glasses was measuredby ion microprobe and by step-heating and was found to be between1 and 2 wt %. The dissolved carbon content was found to be 1600ppm C by step-heating. The speciation of C and H componentswas determined by IR and Raman spectroscopy. It was establishedthat the main part of the liberated oxygen was used to formOH– and to a much lesser extent H2O, and only traces ofH2, CO2 and 相似文献
16.
The Southern Marginal Zone of the Limpopo Belt in South Africa is characterised by a granulite and retrograde hydrated granulite terrane. The Southern Marginal Zone is, therefore, perfectly suitable to study fluids during and after granulite facies metamorphism by means of fluid inclusions and equilibrium calculations. Isolated and clustered high-salinity aqueous and CO2(-CH4) fluid inclusions within quartz inclusions in garnet in metapelites demonstrate that these immiscible low H2O activity fluids were present under peak metamorphic conditions (800-850 °C, 7.5-8.5 kbar). The absence of widespread high-temperature metasomatic alteration indicates that the brine fluid was probably only locally present in small quantities. Thermocalc calculations demonstrate that the peak metamorphic mineral assemblage in mafic granulites was in equilibrium with a fluid with a low H2O activity (0.2-0.3). The absence of water in CO2-rich fluid inclusions is due to either observation difficulties or selective water leakage. The density of CO2 inclusions in trails suggests a retrograde P-T path dominated by decompression at T<600 °C. Re-evaluation of previously published data demonstrates that retrograde hydration of the granulites at 600 °C occurred in the presence of H2O and CO2-rich fluids under P-T conditions of 5-6 kbar and ~600 °C. The different compositions of the hydrating fluid suggest more than one fluid source. 相似文献
17.
Transition from the Zeolite to Prehnite-Pumpellyite Facies in the Karmutsen Metabasites, Vancouver Island, British Columbia 总被引：1，自引：0，他引：1
The upper Triassic Karmutsen metabasites from northeast VancouverIsland, B.C., are thermally metamorphosed by the intrusion ofthe Coast Range Batholith. The amygdaloidal metabasites developedin the outer portion of the contact aureole show a progressivemetamorphism from zeolite to prehnite-pumpellyite facies. Thesize of an equilibrium domain is extremely small for these metabasites,and the individual amygdule assemblages are assumed to be inequilibrium. Two major calcite-free assemblages (+chlorite+quartz)are characteristic: (i) laumontite+pumpellyite+epidote in thezeolite facies and (ii) prehnite+pumpellyite+epidote in theprehnite-pumpellyite facies. The assemblages and compositionsof Ca-Al silicates are chemographically and theoretically interpretedon the basis of the predicted P-T grid for the model basalticsystem, CaO-MgO-A12O3-Fe2O3-SiO2-H2O. The results indicate:(1) local equilibrium has been approached in mineral assemblagesand compositions; (2) the XFe3+ values in the coexisting Ca-Alsilicates decrease from epidote, through pumpellyite to prehnite;(3) with increasing metamorphic grade, the Fe3+ contents ofepidotes in reaction assemblages decrease in the zeolite facies,then increase in the prehnite-pumpellyite facies rocks. Suchvariations in the assemblages and mineral compositions are controlledby a sequence of continuous and discontinuous reactions, andallow delineation of T-XFe3+ relations at constant pressure.The transition from the zeolite to prehnite-pumpellyite faciesof the Karmutsen metabasites is defined by a discontinuous reaction:0·18 laumontite+pumpellyite+0·15 quartz = 1·31prehnite+ 0·78 epidote+0·2 chlorite+ 1·72H2O, where the XFe3+ values of prehnite, pumpellyite and epidoteare 0·03, 0·10 and 0·18, respectively.These values together with available thermodynamic data andour preliminary experimental data are used to calculate theP-T condition for the discontinuous reaction as P = 1·1±0·5 kb and T = 190±30°C. The effectsof pressure on the upper stability of the zeolite facies assemblagesare discussed utilizing T-XFe3+ diagrams. The stability of thelaumontite-bearing assemblages for the zeolite facies metamorphismof basaltic rocks may be defined by either continuous or discontinuousreactions depending on the imposed metamorphic field gradient.Hence, the zeolite and prehnite-pumpellyite facies transitionboundary is multivariant. 相似文献
18.
Corella marbles in the Mary Kathleen Fold Belt were infiltratedby fluids during low-pressure (200-MPa) contact metamorphismassociated with the intrusion of the Burstall granite at 1730–1740Ma. Fluids emanating from the granite [whole-rock (WR) 18O=8.1–8.6%]produced Fe-rich massive and banded garnet—clinopyroxeneskarns [18O(WR)=9.1–11.9%]. Outside the skarn zones, marblemineralogies define an increase in temperature (500 to >575C) and XCO2 (0.05 to >0.12) towards the granite, andmost marbles contain isobarically univariant or invariant assemblagesin the end-member CaO–MgO–Al2O3–SiO2–H2O–CO2system. Marbles have calcite (Cc) 18O and 13C values of 12.3–24.6%and –1.0 to –3.9%, respectively. A lack of down-temperaturemineral reactions in the marbles suggests that pervasive fluidinfiltration did not continue after the thermal peak of contactmetamorphism. The timing of fluid flow probably correspondsto a period of high fluid production and high intrinsic permeabilitiesduring prograde contact metamorphism. The petrology and stableisotope geochemistry of the marbles suggest that these rockswere infiltrated by water-rich fluids. If fluid flow occurredup to the peak of contact metamorphism, the mineralogical andisotopic resetting is best explained by fluids flowing up-temperaturetoward the Burstall granite. However, if fluid flow ceased beforthe peak of regional metamorphism, the fluid flow directioncannot be unambiguously determined. At individual outcrops,marble 18O(Cc) values vary by several permil over a few squaremetres, suggesting that fluid fluxes varied by at least an orderof magnitude on the metre to tens-of-metre scale. Fluids werefocused across lithological layering; however, mesoscopic fracturesare not recognized. The focusing of fluids was possibly viamicrofractures, and the variation in the degree of resettingmay reflect variations in microcrack density and fracture permeability.The marble—skarn contacts represent a sharp discontinuityin both major element geochemistry and 18O values, suggestingthat, at least locally, little fluid flow occurred across thesecontacts. 相似文献
19.
Metamorphic Evolution of Neoproterozoic Manganese Formations and their Country Rocks at Otjosondu, Namibia 总被引：2，自引：0，他引：2
Manganiferous chemical sediments of Neoproterozoic age in Namibiawere subjected to high-T–low-P metamorphism during theDamara Orogeny and display unique phase assemblages. The manganeseformations are embedded in iron formations and siliciclasticcountry rocks. This sequence is petrographically subdividedinto restricted lithotypes which bear specific mineral assemblagesand compositions depending on their protolith type. In puremanganese ores the critical assemblage braunite + haematite+ jacobsite + rhodonite is frequently developed, whereas interlayeredimpure silicate ores bear various proportions of spessartine,Mn3+-bearing andradite–calderite and andradite garnets,rhodonite, manganoan aegirine–augite, aegirine, Ba–K–Na-feldspars,barite and rare kinoshitalite. Petrological constraints derivedfrom country rock lithologies indicate peak metamorphic conditionsof 660–700C at estimated pressures of 35–45 kbar.Numerous Ba-rich pegmatitic veins restricted to the ore horizonstestify to the production of partial melts from siliciclasticstrata within the manganese formations. They are correlatedwith peak pressure conditions between 5 and 6 kbar, accompanyingthe main deformation event and pre-dating the thermal peak.An early H2O-rich generation of fluid inclusions is interpretedas a manifestation of prograde dehydration reactions in theore horizons. This caused hydraulic fracturing of the ores and,subsequently, triggered the formation of partial melts whichintruded the fracture planes in situ. Peak metamorphism thenoccurred under strainfree conditions allowing equilibrium recrystallizationof all minerals to develop. Phase relationships of manganeseoxides and silicates modelled in the system Mn–Fe–Si–Oreveal variable chemical compositions of braunites, jacobsitesand haematites depending on their paragenesis. They indicatevery restricted oxygen reservoirs within specific strata ofthe manganese ores and eliminate a prominent mass exchange evenon a small scale. This is supported by 18O analyses of silicateassemblages which further exclude mass transfer between manganeseores and country rocks, and indicate preservation of the exchangeequilibria during cooling. The uplift path of the sequence canbe constrained using different decrepitation patterns of H2Ofluid inclusions and a syn-to late-metamorphic CO2-rich fluidinclusion population, which indicate high geothermal gradientsof 70C/km and more. The P–T–D evolution of thishigh-T–low-P metamorphic belt conforms with the palaeotectonicsetting of the study area at the southernmost part of the CongoCraton, representing the continental buttress colliding withthe Kalahari Craton during the Pan-African orogeny. KEY WORDS: manganiferous sediments; Damara Orogeny; Namibia; metamorphism; oxygen isotopes; fluid inclusions
*Corresponding author. Present address Institut fr Geowissenschaften und Lithosphrenforschung, Senckenbergstrasse 3, D-35390 Giessen, Germany 相似文献
20.
Petrographic and petrologic investigations of upper amphibolitefacies metacarbonates from the East Humboldt Range core complex,Nevada, provide important constraints on P-T-XCO2 conditionsand fluid flow during metamorphism. Three marble assemblagesare observed [(1)dol+cc+bt+cpx+q+ruscapkspamph; (2) cc+bt+cpx+plag+q+sphscapksp;(3) cc+cpx+plag+q+sphscapksp], all of which equilibrated withrelatively CO2-rich fluid compositions, at P-T conditions of6 kbar and 600–750C. The most recent equilibration eventis recorded in some calcsilicate gneisses where retrograde amphiboleand epidotegarnet replace clinopyroxene and plagioclase, respectively.This is attributed to infiltration of H2O-rich fluids at and/orafter peak metamorphic temperatures, which continued as therocks were cooled and rapidly uplifted after a Tertiary extension-relatedheating event. Likely sources for the retrograde fluids are the abundant pegmatiticleucogranites in the area. Volumetric fluid-rock ratios of 0.02–0.4are required to generate the retrograde assemblage, and observedleucogranite proportions are more than adequate to provide therequired volume of fluid. Estimates of retrograde fluid fluxesrange from 0.25 to 5102 cm3/cm2 for a transient temperaturegradient of 5C/m, to 3103 to 7104 cm3/cm2 for a temperaturegradient of 35C/km. These gradients are characteristic of askarn-type contact metamorphic environment and a regional crustalgeotherm, respectively. They imply different time-scales andlength-scales for the retrograde fluid flow system, with theformer more akin to a contact metamorphic setting with local,meter-scale retrograde fluid flow, and the latter to a regionalmetamorphic setting with regionally high mid- and lower-crustaltemperatures and fluid flow throughout a significant thicknessof the middle crust. Higher gradients are considered more likelygiven the proximity of leucogranites to retrogressed calc-silicategneisses, and the resultant relatively small fluxes are consistentwith a magmatic source. The length-scale of reaction within the retrograde fluid flowsystem was of the order of meters to hundreds of meters andinvolved both pervasive and (later) fracture-controlled down-temperatureflow. Retrograde fluid flow in this terrance, as well as othersdominated by magmatic volatiles, is in the form of multiplediscrete bursts of fluid released in a discontinuous mannerpotentially over long periods of time (1–10 Ma) with locallyvariable thermal gradients along the flow path. 相似文献