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1.
Kistufell: Primitive Melt from the Iceland Mantle Plume   总被引：5，自引：2，他引：5  
This paper presents new geochemical data from Kistufell (64°48'N,17°13'W), a monogenetic table mountain situated directlyabove the inferred locus of the Iceland mantle plume. Kistufellis composed of the most primitive olivine tholeiitic glassesfound in central Iceland (MgO 10·56 wt %, olivine Fo89·7).The glasses are interpreted as near-primary, high-degree plumemelts derived from a heterogeneous mantle source. Mineral, glassand bulk-rock (glass + minerals) chemistry indicates a low averagemelting pressure (15 kbar), high initial crystallization pressuresand temperatures (10–15 kbar and 1270°C), and eruptiontemperatures (1240°C) that are among the highest observedin Iceland. The glasses have trace element signatures (Lan/Ybn<1, Ban/Zrn 0·55–0·58) indicative ofa trace element depleted source, and the Sr–Nd–Pbisotopic ratios (87Sr/86Sr 0·70304–0·70308,143Nd/144Nd 0·513058–0·513099, 206Pb/204Pb18·343–18·361) further suggest a long-termtrace element depletion relative to primordial mantle. HighHe isotopic ratios (15·3–16·8 R/Ra) combinedwith low 207Pb/204Pb (15·42–15·43) suggestthat the mantle source of the magma is different from that ofNorth Atlantic mid-ocean ridge basalt. Negative Pb anomalies,and positive Nb and Ta anomalies indicate that the source includesa recycled, subducted oceanic crustal or mantle component. PositiveSr anomalies (Srn/Ndn = 1·39–1·50) furthersuggest that this recycled source component involves lower oceaniccrustal gabbros. The  相似文献   

2.
The solubility of sulfur as S2– has been experimentallydetermined for 19 silicate melt compositions in the system CaO–MgO–Al2O3–SiO2(CMAS)± TiO2 ± FeO, at 1400°C and 1 bar, using CO–CO2–SO2gas mixtures to vary oxygen fugacity (fO2) and sulfur fugacity(fS2). For all compositions, the S solubility is confirmed tobe proportional to (fS2/fO2)1/2, allowing the definition ofthe sulfide capacity (CS) of a silicate melt as CS = [S](fO2/fS2)1/2.Additional experiments covering over 150 melt compositions,including some with Na and K, were then used to determine CSas a function of melt composition at 1400°C. The resultswere fitted to the equation  相似文献   

3.
Experimental studies were carried out to evaluate phase relationsinvolving titanite–F–Al-titanite solid solutionin the system CaSiO3–Al2SiO5–TiO2–CaF2. Theexperiments were conducted at 900–1000°C and 1·1–4·0GPa. The average F/Al ratio in titanite solid solution in theexperimental run products is 1·01 ± 0·06,and XAl ranges from 0·33 ± 0·02 to 0·91± 0·05, consistent with the substitution [TiO2+]–1[AlF2+]1.Analysis of the phase relations indicates that titanite solidsolutions coexisting with rutile are always low in XAl, whereasthe maximum XAl of titanite solid solution occurs with fluoriteand either anorthite or Al2SiO5. Reaction displacement experimentswere performed by adding fluorite to the assemblage anorthite+ rutile = titanite + kyanite. The reaction shifts from 1·60GPa to 1·15 ± 0·05 GPa at 900°C, from1·79 GPa to 1·375 ± 0·025 GPa at1000°C, and from 1·98 GPa to 1·575 ±0·025 GPa at 1100°C. The data show that the activityof CaTiSiO4O is very close to the ideal molecular activity model(XTi) at 1100°C, but shows a negative deviation at 1000°Cand 900°C. The results constrain  相似文献   

4.
La Pacana is one of the largest known calderas on Earth, andis the source of at least two major ignimbrite eruptions witha combined volume of some 2700 km3. These ignimbrites have stronglycontrasting compositions, raising the question of whether theyare genetically related. The Toconao ignimbrite is crystal poor,and contains rhyolitic (76–77 wt % SiO2) tube pumices.The overlying Atana ignimbrite is a homogeneous tuff whose pumiceis dacitic (66–70 wt % SiO2), dense (40–60% vesicularity)and crystal rich (30–40 % crystals). Phase equilibriaindicate that the Atana magma equilibrated at temperatures of770–790°C with melt water contents of 3·1–4·4wt %. The pre-eruptive Toconao magma was cooler (730–750°C)and its melt more water rich (6·3–6·8 wt% H2O). A pressure of 200 MPa is inferred from mineral barometryfor the Atana magma chamber. Isotope compositions are variablebut overlapping for both units (87Sr/86Sri 0·7094–0·7131;143Nd/144Nd 0·51222–0·51230) and are consistentwith a dominantly crustal origin. Glass analyses from Atanapumices are similar in composition to those in Toconao tubepumices, demonstrating that the Toconao magma could representa differentiated melt of the Atana magma. Fractional crystallizationmodelling suggests that the Toconao magma can be produced by30% crystallization of the observed Atana mineral phases. Toconaomelt characteristics and intensive parameters are consistentwith a volatile oversaturation-driven eruption. However, thelow H2O content, high viscosity and high crystal content ofthe Atana magma imply an external eruption trigger. KEY WORDS: Central Andes; crystal-rich dacite; eruption trigger; high-silica rhyolite; zoned magma chamber  相似文献   

5.
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   

6.
The basement of Sardinia represents a nearly complete sectionof a segment of the Variscan belt that experienced a polyphasetectono-metamorphic evolution and Barrovian metamorphism. Thisbasement is well suited to investigate the relationship betweentectono-metamorphic evolution and argon isotope records in whitemica. Micaschists from the garnet zone (maximum T of up to 520–560°C)contain two texturally and chemically resolvable generationsof white mica: (1) deformed celadonite-rich flakes, defininga relict S1 foliation preserved within the main S2 foliationor enclosed in rotated albite porphyroblasts; (2) celadonite-poorwhite micas aligned along the main S2 foliation. The S1 foliationdeveloped earlier and at a deeper crustal level with respectto that at which the thermal peak was reached. From the staurolitezone (T of up to 590–625°C) to the sillimanite + K-feldsparzone, white mica is nearly uniform in composition (muscovite)and is predominantly aligned along the S2 foliation or is oflater crystallization. In situ 40Ar–39Ar laser analysesof white mica yielded ages of  相似文献   

7.
The bronzite—chromite-anorthite assemblage of the F—unit(Cameron & Emerson, 1959) from the Critical Zone of theBushveld Igneous Complex, was examined with the aid of an electrolyticcell designed after Sato (1971). The resultant fO2-T data reveala last equilibration at an fO2 value of 1011·82 ±·40 atm and at a temperature of 1091 ± 35 °C.These fO2-T data when compared with: (1) a one atmosphere quenching—technique solidus determinationof 1110 ± 5 °C, (2) the Bushveld plagioclase compositional trends (Cameron,1970), (3) Bushveld petrofabric examinations (Cameron, 1969) (4) phase equilibria in the system CaO–MgO–FeO–CaAl2Si2O8–SiO2(Roeder & Osborn, 1966), (5) phase equilibria in the system CaAl2Si2O8–NaAlSi3O8–SiO2–MgO–Fe–O2–H2O–CO2(Eggler, 1974), all support the idea that the Eastern Bushveld magma was notappreciably differentiating in the middle Critical Zone betweenF and the L Horizons, an accumulation of nearly 220 meters.  相似文献   

8.
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   

9.
Miocene to Recent volcanism in northwestern Arabia producedthe largest intraplate volcanic field on the Arabian plate (HarratAsh Shaam, Jordan). The chemically and isotopically diversevolcanic field comprises mafic alkali basalts and basanites.The magmas underwent limited fractional crystallization of ol± cpx ± plag and rare samples have assimilatedup to 20% of Late Proterozoic crust en route to the surface.However, there are subtle Sr–Nd–Pb isotopic variations(87Sr/86Sr = 0·70305–0·70377, 143Nd/144Nd= 0·51297–0·51285, 206Pb/204Pb = 18·8–19·2),which exhibit marked correlations with major elements, incompatibletrace element ratios and abundances in relatively primitivebasalts (MgO >8·5 wt %), and cannot be explained byfractional crystallization and crustal contamination alone.Instead, the data require polybaric melting of heterogeneoussources. Semi-quantitative melt modelling suggests that thisheterogeneity is the result of small degree melts (2–5%)from spinel- and garnet-facies mantle, inferred to be shallowArabian lithosphere, that mixed with smaller degree melts (<1%)from a predominantly deep garnet-bearing asthenospheric(?) sourcewith ocean island basalt characteristics. The latter may bea ubiquitous part of the asthenosphere but is preferentiallytapped at small degrees of partial melting. Volcanism in Jordanappears to be the result of melting lithospheric mantle in responseto lithospheric extension. With time, thinning of the lithosphereallowed progressively deeper mantle (asthenosphere?) to be activatedand melts from this to mix with the shallower lithospheric mantlemelts. Although Jordanian intraplate volcanism is isotopicallysimilar to examples of Late Cenozoic volcanism throughout theArabian peninsula (Israel, Saudi Arabia), subtle chemical andisotopic differences between Yemen and Jordan intraplate volcanismsuggest that the Afar plume has not been channelled northwestwardsbeneath the Arabian plate and played no role in producing thenorthern Saudi Arabian and Jordan intraplate volcanic fields. KEY WORDS: asthenosphere; intraplate volcanism; Jordan; lithospheric mantle; Sr–Nd–Pb isotopes  相似文献   

10.
The volcanic activity of Mts Bambouto and Oku (Western Highlands)and of the Ngaoundere Plateau, in the continental sector ofthe Cameroon Volcanic Line, Equatorial West Africa, ranges inage from Oligocene to Recent. It is characterized by basanitic,alkali basaltic and transitional basaltic series. Mineral chemistry,major and trace element bulk-rock compositions, and geochemicalmodelling suggest that the magmatic series evolved mainly atlow pressure (2–4 kbar) through fractional crystallizationof clinopyroxene and olivine ± magnetite, at moderatelyhydrated (H2O = 0·5–1 wt %) and QFM (quartz–fayalite–magnetite)to QFM + 1 fO2 conditions. Basalts from Ngaoundere (Mioceneto Quaternary) and from the early activity (31–14 Ma)of the Western Highlands have incompatible trace element andSr–Nd isotopic compositions similar to those of oceanicCameroon Line basalts, pointing to a similar asthenosphericmantle source. By contrast, the late (15–4 Ma) WesternHighlands basanites and alkali basalts have anomalously highconcentrations of Sr, Ba and P, and low concentrations of Zr,which are exclusive features of continental Cameroon basalts.The genesis of these latter magmas is consistent with derivationfrom an incompatible element enriched, amphibole-bearing lithosphericmantle source. Western Highlands basalts show a continuous spectrumfrom high to low Sr–Ba–P compositions, and may resultfrom variable amounts of mixing between melts derived from ananhydrous lherzolite source (asthenospheric component) and meltsfrom an amphibole-bearing peridotite source (lithospheric HSrcomponent). New 40Ar/39Ar ages for Mts Oku and Bambouto basalts,combined with previous 40Ar/39Ar and K/Ar ages of basaltic andsilicic volcanics, and with volcanic stratigraphy, suggest aNE–SW younging of the peak magmatic activity in the WesternHighlands. This SW younging trend, extending from the Oligocenevolcanism in northern Cameroon (e.g. Mt Oku) to the still activeMt Cameroon, suggests that the African plate is moving abovea deep-seated mantle thermal anomaly. However, the age and locationof the Ngaoundere volcanism does not conform to the NE–SWyounging trend, implying that the continental sector of theCameroon Volcanic Line cannot be easily interpreted as the surfaceexpression of a single hotspot system. KEY WORDS: Cameroon Line basalts;40Ar/39Ar geochronology; lithospheric and asthenospheric mantle source; hotspot  相似文献   

11.
Crystallization experiments were performed at 200 MPa in thetemperature range 1150–950°C at oxygen fugacitiescorresponding to the quartz–fayalite–magnetite (QFM)and MnO–Mn3O4 buffers to assess the role of water andfO2 on phase relations and differentiation trends in mid-oceanridge basalt (MORB) systems. Starting from a primitive (MgO9·8 wt %) and an evolved MORB (MgO 6·49 wt %),crystallization paths with four different water contents (0·35–4·7wt % H2O) have been investigated. In primitive MORB, olivineis the liquidus phase followed by plagioclase + clinopyroxene.Amphibole is present only at water-saturated conditions below1000°C, but not all fluid-saturated runs contain amphibole.Magnetite and orthopyroxene are not stable at low fO2 (QFM buffer).Residual liquids obtained at low fO2 show a tholeiitic differentiationtrend. The crystallization of magnetite at high fO2 (MnO–Mn3O4buffer) results in a decrease of melt FeO*/MgO ratio, causinga calc-alkaline differentiation trend. Because the magnetitecrystallization temperature is nearly independent of the H2Ocontent, in contrast to silicate minerals, the calc-alkalinedifferentiation trend is more pronounced at high water contents.Residual melts at 950°C in a primitive MORB system havecompositions approaching those of oceanic plagiogranites interms of SiO2 and K2O, but have Ca/Na ratios and FeO* contentsthat are too high compared with the natural rocks, implyingthat fractionation processes are necessary to reach typicalcompositions of natural oceanic plagiogranites. KEY WORDS: differentiation; MORB; oxygen fugacity; water activity; oceanic plagiogranite  相似文献   

12.
High-pressure–high-temperature experiments were performedin the range 7–15 GPa and 1300–1600°C to investigatethe stability and phase relations of the K- and Ba-dominantmembers of the crichtonite and magnetoplumbite series of phasesin simplified bulk compositions in the systems TiO2–ZrO2–Cr2O3–Fe2O3–BaO–K2Oand TiO2–Cr2O3–Fe2O3–BaO–K2O. Both seriesof phases occur as inclusions in diamond and/or as constituentsof metasomatized peridotite mantle xenoliths sampled by kimberlitesor alkaline lamprophyres. They can accommodate large ion lithophileelements (LILE) and high field strength elements (HFSE) on awt % level and, hence, can critically influence the LILE andHFSE budget of a metasomatized peridotite even if present onlyin trace amounts. The Ba and K end-members of the crichtoniteseries, lindsleyite and mathiasite, are stable to 11 GPa and1500–1600°C. Between 11 and 12 GPa, lindsleyite breaksdown to form two Ba–Cr-titanates of unknown structurethat persist to at least 13 GPa. The high-pressure breakdownproduct of mathiasite is a K–Cr-titanate with an idealizedformula KM7O12, where M = Ti, Cr, Mg, Fe. This phase possessesspace group P63/m with a = 9·175(2) Å, c = 2·879(1)Å, V = 209·9(1) Å3. Towards high temperatures,lindsleyite persists to 1600°C, whereas mathiasite breaksdown between 1500 and 1600°C to form a number of complexTi–Cr-oxides. Ba and K end-members of the magnetoplumbiteseries, hawthorneite and yimengite, are stable in runs at 7,10 and 15 GPa between 1300 and 1400°C coexisting with anumber of Ti–Cr-oxides. Molar mixtures (1:1) of lindsleyite–mathiasiteand hawthorneite–yimengite were studied at 7–10GPa and 1300–1400°C, and 9–15 GPa and 1150–1400°C,respectively. In the system lindsleyite–mathiasite, onehomogeneous Ba–K phase is stable, which shows a systematicincrease in the K/(K + Ba) ratio with increasing pressure. Inthe system hawthorneite–yimengite, two coexisting Ba–Kphases appear, which are Ba rich and Ba poor, respectively.The data obtained from this study suggest that Ba- and K-dominantmembers of the crichtonite and magnetoplumbite series of phasesare potentially stable not only throughout the entire subcontinentallithosphere but also under conditions of an average present-daymantle adiabat in the underlying asthenosphere to a depth ofup to 450 km. At still higher pressures, both K and Ba may remainstored in alkali titanates that would also be eminently suitablefor the transport of other ions with large ionic radii. KEY WORDS: crichtonite; magnetoplumbite; high-P–T experiments; phase relations; upper mantle  相似文献   

13.
Low-Pressure Experimental Constraints on the Evolution of Komatiites   总被引：1，自引：0，他引：1  
THY  P. 《Journal of Petrology》1995,36(6):1529-1548
Melting experiments were performed on a komatiitic basalt with17 wt% MgO from Munro Township, Ontario, at I-atm pressure andan oxygen fugacity controlled approximately to the fayalite-magnetite-quartzbuffer. The experiments showed that olivine appears at 1344±5°C,spinel at 1334±6°C plagioclase at 1185±5°C,augite at 1176±5°C and pigeonite at 1154±6°C.Compositionally, olivine varies from Fo90 to Fo74 and displaysan average KFe/MgD (ol/liq) of 0•32. The spinels are chromitesand chromian spinels with Mg/(Mg + Fe2+) ratios between 0•66and 0•;32, which show a marked correlation with meltingtemperature. The pyroxenes show an average KFe/MgD (px/liq)of 0•26, identical for augite and pigeonite. Plagiodaseranges compositionally between An82 and An72 Plotted in thepseudo-quaternary basalt phase diagram, the liquid line of descentis similar to that observed for quartz tholeiitic magmas. Therefore,the low-pressure, late-stage evolution products of komatiiteand basaltic komatiite parental magmas will chemically and mineralogicallybe ferrobasaltic quartz tholeiites. High-temperature and high-pressuremodeling suggests that the main observed compositional variationof Munro komatiites can be explained by low-pressure crystalfractionation and accumulation of olivine into komatiite liquidswith below 21•5–23•5 wt% MgO and eruptive temperaturesbelow 1435–1465°C for oxygen fugacities between thefayalite-magnetite quartz (FMQ) and iron-wiistite (IW) buffers.The maximum magnesium content of liquid komatiites, assumingequilibrium Fo94 olivine, is 27–29 wt% MgO and eruptivetemperatures are between 1515 and 1540°C. KEY WORDS: komatiites; experimental petrology; Munro Township; Ontario  相似文献   

14.
We present elemental and isotopic (Sr–Nd–Pb–Hf–Os–He)data on primitive alkalic lavas from the Prinsen af Wales Bjerge,East Greenland. Stratigraphical, compositional and 40Ar–39Ardata indicate that this inland alkalic activity was contemporaneouswith the upper parts of the main tholeiitic plateau basaltsand also post-dated them. The alkalic rocks show a marked crustalinfluence, indicating establishment of new magmatic plumbingsystems distinct from the long-lived coastal systems that fedthe relatively uncontaminated plateau basalts. The least contaminatedlavas have high 3He/4He isotope ratios (R/RA 12·4–18·5),sub-chondritic 187Os/188Osi (0·120–0·126),low  相似文献   

15.
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   

16.
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   

17.
FERRY  JOHN M. 《Journal of Petrology》1995,36(4):1039-1053
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   

18.
Experimental phase equilibrium data on compositions of coexistingpyroxenes in the quadrilateral enstatite-diopside-ferrosilite-hedenbergitehave been used to model pyroxene solid solutions and to formulatepyroxene geothermometers. Each pyroxene is treated as a solidsolution of four quad-components using the Kohler formulation where Gij* is the excess free energy of mixing in a binary solutioncalculated with binary mole fractions (e.g. Xio = Xi/(Xi+Xj))and Xi is the mole fraction in a multicomponent solution. Thefit to the experimental data is achieved by minimizing the totalGibbs free energy of the assemblage. The following set of thermochemicaldata and simple mixture parameters (Wij) are found to be bestsuited. Standard (T = 298?15 K) enthalpy and entropy of formationfrom elements for fictive orthohedenbergite are –1416?8kJ and 84?88 J K–1 mol –1 respectively. The heatcapacity is given by 114?67+17?09E-3T–31?40E5T–2.The Wij data are: Opx: W12 = W21 = 25 W13 = (13?1–0-015T),W31 = (3?37–0?005T), W23 = 20, W32 = 16, W24 = 5, W42= 7, W34 = 15, W43 = 15; Cpx: W12 = (25?484+0?0812P), W21 =(31?216–0?0061P),W31 = W13 = 0W14 = (93?3–0?045T), W41 = (–20?0+0?028T),W23 = 24, W32 = 15, W24 = 12, W42 = 12, W34 = (16?941+0?00592P),W43 = (20?697–0?00235P). Coexisting pyroxene compositionshave been computed in the temperature range of 700 to 1400?C. Two geothermometers have been constructed, one based on atomicfraction of iron (Fe/(Fe + Mg)) in orthopyroxene and the Fe-Mgdistribution coefficient and the other, based on wollastonitecontent of clinopyroxene. The two scales yield different temperatureswhen applied to the same rock. In igneous pyroxenes, the Catransfer ceased at 150 to 200?C above the closure temperatureof the Fe-Mg ion-exchange. In metamorphic rocks an oppositeeffect seems to have prevailed.  相似文献   

19.
The Cretaceous lava sequence and associated mafic dyke swarmin central–western Madagascar (Mailaka and Bemaraha areas)range in composition from picrite basalts to cordierite–orthopyroxene-bearingrhyodacites (MgO from 14 to 0·6 wt %). Petrographic andchemical data indicate the presence of both tholeiitic and transitionalmagma series, with variable degree of rare earth element enrichment[(La/Nd)n = 1–1·4 for tholeiites vs (La/Nd)n =0·65–1 for transitional rocks]. Initial (at 88Ma) 87Sr/86Sr and  相似文献   

20.
Anhydrite solubility in H2O–NaCl solutions was measuredat 6–14 kbar, 600–800°C and NaCl mole fractions(XNaCl) of 0–0·3 in piston–cylinder apparatus.Solubilities were determined by weight changes of natural anhydritein perforated Pt envelopes confined with fluid in larger Ptcapsules. In initially pure H2O at 10 kbar and 800°C, CaSO4concentration is low (0·03 molal), though much largerthan at the same temperature and 1 kbar. Hematite-buffered experimentsshowed slightly lower solubilities than unbuffered runs. CaSO4solubility increases enormously with NaCl activity: at 800°Cand 10 kbar and XNaCl of 0·3, CaSO4 molality is 200 timeshigher than with pure H2O. Whereas CaSO4 solubility in pureH2O decreases with rising T at low T and P, the high-P resultsshow that anhydrite solubility increases with T at constantP at all XNaCl investigated. The effects of salinity and temperatureare so great at 10 kbar that critical mixing between sulfate-richhydrosaline melts and aqueous salt solutions is probable at900°C at XNaCl 0·3. Recent experimental evidencethat volatile-laden magmas crystallizing in the deep crust mayevolve concentrated salt solutions could, in light of the presentwork, have important implications regarding such diverse processesas Mount Pinatubo-type S-rich volcanism, high-f O2 regionalmetamorphism, and emplacement of porphyry Cu–Mo ore bodies,where anhydrite–hematite alteration and fluid inclusionsreveal the action of very oxidized saline solutions rich insulfur. KEY WORDS: anhydrite; sulfur; solubility; metamorphic brines; granulites  相似文献   

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