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1.
Carbon-isotope analysis of CO2 has been undertaken on pure mineralseparates from six cordierite-bearing assemblages from Kerala,South India, to identify the significance of fluid inclusionsand channel-trapped volatiles in cordierite. Field relations,phase-equilibria systematics, and fluidinclusion studies suggestthat cordierite megacrysts associated with orthopyroxene withincharnockites have grown during an influx of CO2 post-datingregional metamorphism, in a process equivalent to incipient-charnockiteformation in rocks of lower Mg/Fe ratios. In contrast, smallercordierite grains associated with sillimanite and spinel, definingcompositional bands in the metapelitic assemblages, have formedduring the earlier regional metamorphism, although for one ofthese samples a subsequent period of local cordierite growthduring channelized CO2 influx has been identified. CO2 has been extracted from fluid inclusions in quartz, garnet,and cordierite by a stepped-heating technique, and its abundanceand carbon-isotope values determined in each case. Althoughunimodal release patterns generally characterize fluids releasedfrom quartz and garnet, for cordierite a strongly bimodal releaseprofile is observed. At 500–700C volatiles are extractedfrom fluid inclusions in quartz, cordierite, and garnet, whereasabove 800C CO2 release from cordierite is correlated with theexpulsion of channel volatiles. Isotopic results confirm thatchannel-derived volatiles and fluid inclusions in cordieriteretain similar l3C values in samples where cordierite is interpretedto have grown during CO2 influx (13C= –5 to –8%),whereas pre-influx CO2 can be retained in the channels of cordieritewhich predates the influx event. For cordierite-bearing metapelitesthat have not been subjected to fluid influx, carbonic inclusionsare virtually absent from cordierite. The results suggest that CO2 is trapped in cordierite channelsduring mineral growth, with little isotopic re-equilibrationduring subsequent events. Studies of fluid release from cordieritescan therefore yield important information on the evolution ofmetamorphic fluids provided that (1) fluidinclusion releaseand channel-derived volatiles can be distinguished analytically,and (2) the chronology of cordierite growth and fluid entrapmentin both channels and inclusions can be constrained. *Present address: Centre for Earth Science Studies, Akkulam, Trivandrum 695-031, India Reprint requests to N. B. W. Harris  相似文献   

2.
Mid-Proterozoic ( 1000 Ma) granulite facies calc-silicates fromthe Rauer Group, East Antarctica, contain grossular-wollastonite-scapolite-dinopyroxene( + quartz or calcite) assemblages which preserve symplectiteand corona textures typically involving the growth of secondarywollastonite. The textures include (1) wollastonite rims betweenquartz and calcite; (2) wollastonite-plagioclase rims and intergrowthsbetween quartz and scapolite; (3) wollastonite-scapolite-clinopyroxeneinter-growths replacing grossular; and (4) wollastonite-plagioclasesymplectites replacing grossular or earlier symplectites (3). Reactions between grossular, scapolite, wollastonite, calcite,quartz, anorthite, and vapour, have been modelled in the CaO-Al2O3SiO2-H2O-CO2and more complex systems using the internally consistent data-setof Holland & Powell (1990). Reactions producing scapoliteand wollastonite consume vapour as temperature increases (i.e., carbonation), in agreement with the results of Moecher &Essene (1990). These calc-silicates can therefore behave asfluid sinks under high-grade conditions. Conversely, they maybe important fluid sources on cooling and contribute to theformation of post-metamorphic CO2rich fluid inclusions in isobaricallycooled granulites. P-T-CO2 diagrams calculated for typical phase compositions (e.g., garnet, scapolite) demonstrate that the observed texturesare a record of near-isothermal decompression at 800–850 C, consistent with P—rpath determinations based on otherrock types from the Rauer Group. For example, texture (2) resultsfrom crossing the reaction Scapolite + Quartz = Wollastonite + Plagioclase + V on decompression, at 6. 5–7 kb, 820 C, and aCO2 of0–4–0–5. Furthermore, correlations betweenmodes of product phases (e. g., wollastonitexlinopyroxene) andreactant garnet composition preclude open-system behaviour inthe formation of these textures, consistent with post-peak vapour-absentreactions such as Grossular + Calcite + Quartz = Wollastonite + Scapolite occurring on decomposition at high temperatures (>800C). Reaction textures developed in calc-silicates from other granuliteterranes often involve the formation of grossular ( + quartz calcite) as rims on wollastonite-scapolite, or replacementof wollastonite by calcite-quartz. These textures have developedprincipally in response to cooling below 780–810 C andmay be signatures of near-isobaric cooling. Infiltration ofhydrous fluid is not a necessary condition for the productionof garnet coronas in wollastonite-scapolite granulites. *Present address: Department of Earth Sciences, University ofMelbourne, Parkville, Victoria 3052, Australia  相似文献   

3.
Proterozoic migmatitic paragneisses exposed in the McCulloughRange, southern Nevada, consist of cordierite+almanditic garnet+biotite+sillimanite+plagioclase+K-feldspar+quartz+ilmenite+hercynite.This assemblage is indicative of a low-pressure fades seriesat hornblende-granulite grade. Textures record a single metamorphicevent involving crystallization of cordierite at the expenseof biotite and sillimanite. Thermobarometry utilizing cation exchange between garnet, biotite,cordierite, hercynite, and plagioclase yields a preferred temperaturerange of 590–750?C and a pressure range of 3–4 kb.Equilibrium among biotite, sillimanite, quartz, garnet, andK-feldspar records aH2O between 0?03 and 0?26. The low aH2Otogetherwith low fO2 (QFM) and optical properties of cordierite indicatemetamorphism under fluid-absent conditions. Preserved mineralcompositions are not consistent with equilibrium with a meltphase. Earlier limited partial melting was apparently extensiveenough to cause desiccation of the pelitic assemblage. The relatively low pressures attending high-grade metamorphismof the McCullough Range paragneisses allies this terrane withbiotite-cordierite-garnet granulites in other orogenic belts.aosure pressures and temperatures require a transient apparentthermal gradient ofat least 50?C/km during part of this Proterozoicevent in the southern Cordillera. *Present address: Institute of Geophysics and Planetary Physics, University of California, Los Angeles, CA 90024-1567  相似文献   

4.
Dehydration-melting of Biotite Gneiss and Quartz Amphibolite from 3 to 15 kbar   总被引：80，自引：20，他引：60  
We performed vapor-absent melting and crystallization experimentson two bulk compositions that model metamorphic rocks containinga single hydrous phase: a biotite gneiss [37% bio (mg-number55), 34% qtz, 27% plg (An38), 2% ilm] and a quartz amphibolite[54% hbl (mg-number 60), 24% qtz, 20% plg (An38), 2% ilm]. Experimentswere performed at 3 and 5 kbar in internally heated pressurevessels (IHPV), and at 7, 10, 125 and 15 kbar in piston cylinderapparatus (PC), from the vapor-absent solidi to (at least) thetemperature at which the hydrous mineral disappeared. Dehydration-meltingbegins at similar temperatures in both bulk compositions, rangingfrom T850C at P = 3 kbar T930C at P = 15 kbar. The hydrousmineral disappears 50C above the solidus in both systems, exceptin IHPV experiments at f(O2) above Ni–NiO, in which biotitestability extends up to atleast 80C above the solidus. At theT at which the hydrous minerals disappear the biotite gneissproduces 2–3 times more melt than the quartz amphibolite(50–60 wt% vs 20–30 wt%). In both systems, variationsin melt productivity with P are controlled by three competingfactors: (1) the positive d P/dT slopes of the solidi, (2) decreasingH2O activity with increasing P at constant H2O content, and(3) Na2O activity, which increases with P concomitantly withbreakdown of plagioclase. Melt productivities at T = 920–950Care maximized at intermediate pressures (7 kbar). The biotitegneiss produces strongly peraluminous granitic melts (SiO2>70wt%) and residual assemblages of quartz norite (P>125 kbar)or garnet pyroxenite (P>125 kbar). The quartz amphiboliteproduces strongly peraluminous granodioritic melts (SiO2>70wt%) that coexist with clinopyroxene + orthopyroxene + plagioclase+ quartz at P>10 kbar)garnet. The results of coupled meltingand crystallization experiments on the quartz amphibolite suggestthat strongly peraluminous granitoid rocks (e.g. cordierite-bearingand two-mica granites) can be derived from melting of Al-poorprotoliths. KEY WORDS: dehydration-melting; biotite gneiss; amphibolite; felsic magmas *Corresponding author  相似文献   

5.
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   

6.
At Kabbaldurga, infiltration of carbonic fluids along a systemof ductile shears and foliation planes has led to partial transformationof Archaean grey biotite–hornblende gneiss to coarse-grainedmassive charnockite at about 2.5 b.y. ago. The dehydration ofthe gneiss assemblage was induced by a marked metasomatic changeof the reacting system from granodioritic to granitic, and obviouslytook place under conditions of an open system at 700–750?C and 5–7 kb. Extensive replacement of plagioclase (An16–30)by K-feldspar through Na, Ca–K exchange reactions withthe ascending carbonic fluids led to strong enrichment in K,Rb, Ba, and SiO2, and to a depletion in Ca. Progressive dissolutionof hornblende, biotite, magnetite, and the accessory mineralsapatite and zircon resulted in a marked depletion in Fe, Mg,Ti, Zn, V, P, and Zr. Most important is the recognition of REEmobility: with advancing charnockitization, the moderately fractionatedREE distribution patterns of the grey gneisses (LaN270; LaN/YbN= 5–20; EuN27; Eu/Eu* = 0.6–0.3) give way to stronglyfractionated REE patterns with a positive Eu-anomaly (LaN200;LaN/YbN = 20–80; EuN22; Eu/Eu* = 0.6–1.8). The systematicdepletion especially in the HREE is due to the progressive dissolutionof zircon, apatite (and monazite), which strongly concentratethe REE. Stable isotope data (18O of 6.9–8.0 per mille for gneissesand charnockites; 13C of –8.5 and –6.5 per millefor late carbonate) indicate a magmatogenic source for the carbonicfluids. In contrast to the currently favoured derivation ofcarbonic fluids by decarbonation of the upper mantle or degassingof underplated basaltic intrusions, it is discussed here thatabundant fluid inclusions in lower crustal charnockites providedan extensive reservoir of ‘fossil’ carbonic fluids.Shear deformation has tapped this reservoir and generated thechannel-ways for fluid ascent. Charnockitization of the Kabbaldurgatypethus appears to be a metasomatic process which is tectonicallycontrolled and restricted to the crustal level of the amphiboliteto granulite transition.  相似文献   

7.
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   

8.
Sapphirine granulite occurring as lenses in charnockite at Anantagiri,Eastern Ghat, India, displays an array of minerals which developedunder different P-T-X conditions. Reaction textures in conjunctionwith mineral chemical data attest to several Fe-Mg continuousreactions, such as
  1. spinel+rutile+quartz+MgFe–1=sapphirine+ilmenite
  2. cordierite=sapphirine+quartz+MgFe–1
  3. sapphirine+quartz=orthopyroxene+sillimanite+MgFe–1
  4. orthopyroxene+sapphirine+quartz=garnet+MgFe–1
  5. orthopyroxene+sillimanite=garnet+quartz+MgFe–1
  6. orthopyroxene+sillimanite+quartz+MgFe–1=cordierite.
Calculated positions of the reaction curves in P-T space, togetherwith discrete P-T points obtained through geothermobarometryin sapphirine granulite and the closely associated charnockiteand mafic granulite, define an anticlockwise P-T trajectory.This comprises a high-T/P prograde metamorphic path which culminatedin a pressure regime of 8?3 kb above 950?C, a nearly isobariccooling (IBC) path (from 950?C, 8?3 kb, to 675?C, 7?5kb) anda terminal decompressive path (from 7?5 to 4?5 kb). Spinel,quartz, high-Mg cordierite, and sapphirine were stabilized duringthe prograde high-T/P metamorphism, followed by the developmentof orthopyroxene, sillimanite, and garnet during the IBC. Retrogradelow-Mg cordierite appeared as a consequence of decompressionin the sapphirine granulite. Deformational structures, reportedfrom the Eastern Ghat granulites, and the available geochronologicaldata indicate that prograde metamorphism could have occurredat 30001?00 and 2500?100 Ma during a compressive orogeny thatwas associated with high heat influx through mafic magmatism. IBC ensued from Pmax and was thus a direct consequence of progrademetamorphism. However, in the absence of sufficient study onthe spatial variation in P-T paths and the strain historiesin relation to time, the linkage between IBC and isothermaldecompression (ITD) has remained obscure. A prolonged IBC followedby ITD could be the consequence of one extensional mechanismwhich had an insufficient acceleration at the early stage, orITD separately could be caused by an unrelated extensional tectonism.The complex cooled nearly isobarically from 2500 Ma. It sufferedrapid decompression accompanied by anorthosite and alkalinemagmatism at 1400–1000 Ma.  相似文献   

9.
We have determined the Fe-Mg fractionation between coexistinggarnet and orthopyroxene at 20–45 kb, 975–1400?C,and the effect of iron on alumina solubility in orthopyroxeneat 25 kb, 1200?C, and 20 kb, 975?C in the FMAS system. The equilibriumcompositions were constrained by experiments with crystallinestarting mixtures of garnet and orthopyroxene of known initialcompositions in graphite capsules. All iron was assumed to beFe2+. A mixture of PbO with about 55 mol per cent PbF2 provedvery effective as a flux. The experimental results do not suggest any significant dependenceof KD on Fe/Mg ratio at T 1000?C. The lnKD vs. l/T data havebeen treated in terms of both linear and non-linear thermodynamicfunctional forms, and combined with the garnet mixing modelof Ganguly & Saxena (1984) to develop geothermometric expressionsrelating temperature to KD and Ca and Mn concentrations in garnet. The effect of Fe is similar to that of Ca and Cr3+ in reducingthe alumina solubility in orthopyroxene in equilibrium withgarnet relative to that in the MAS system. Thus, the directapplication of the alumina solubility data in the MAS systemto natural assemblages could lead to significant overestimationof pressure, probably by about 5 kb for the relatively commongarnetlherzolites with about 25 mol per cent Ca+Fe2+ in garnetand about 1 wt. per cent Al2O3 in orthopyroxene.  相似文献   

10.
In the early Proterozoic Wopmay Orogen (Northwest Territories,Canada), the occurrence of garnet-biotite-sillimanite/kyanite-plagioclase-quartzassemblages in pelitic schists at a variety of obliquely exposedstructural levels enables the use of calibrated geothermometersand geobarometers through 30 km of composite structural relief.Direct derivation of multipoint P-T paths from single garnetsis attained from core-to-rim microprobe analyses of zoned poikiloblasticgarnets, which contain biotite, plagioclase, quartz, and lesscommonly Al2SiO5 inclusions. The documented garnet zoning andthe entrapment of the mineral inclusions is compatible withpartial-equilibrium growth models. The lack of significant diffusionre-equilibration in the garnet interiors is favored by samplerestriction to medium-grade schists and is attested by the preservationof normal-zoning profiles, the lack of garnet diffusion babesaround biotite inclusions, the matching composition trends ofgarnet-core to -rim plagioclase inclusions with those of zonedmatrix plagioclase grains, and the systematic variation of thederived P-T data. Only the garnet rims, which are characterizedby a reversal of compositional trends and by textural resorption,are interpreted to indicate local post-thermal-peak re-equilibration. The calculated P-T paths quantify segments of uplift trajectoriescorresponding to pressure drops of 2?5–1?5 kb from maximaof 9?3–5?0 kb depending on structural level. This is concurrentwith initial increases of 25–75?C to peak-temperatureconditions and is followed by variable drops in temperatureduring continued decompression. Individual paths are consistentwith modelled variations of metamorphic conditions as a functionof loading, uplift, and erosion in overthrust terrains. Consideredwith U-Pb zircon geochronological data the P-T paths, studiedas a set, indicate an average uplift rate that varies spatiallyfrom 1?5–2?7 mm y–1. This variation can be relatedto late cross folding of the orogenic internal zone, suggestingthat the syn-metamorphic uplift was structurally controlled.The distribution of peak-temperature conditions attained duringdecompression is independent of structural depth. This, andthe inverted metamorphism documented in the Wopmay Orogen, requirethat final variations in temperature result from thermal relaxationof isotherms in, and away from, a hot crustal allochthon composedin part of high-T rift-fill units and a syntectonic graniticbatholith.  相似文献   

11.
Four natural peridotite nodules ranging from chemically depletedto Fe-rich, alkaline and calcic (SiO2 = 43.7–45.7 wt.per cent, A12O3 = 1.6O–8.21 wt. per cent, CaO = 0.70–8.12wt. per cent, alk = 0.10–0.90 wt. per cent and Mg/(Mg+Fe2+)= 0.94–0.85) have been investigated in the hypersolidusregion from 800? to 1250?C with variable activities of H2O,CO2, and H2. The vapor-saturated peridotite solidi are 50–200?Cbelow those previously published. The temperature of the beginningof melting of peridotite decreases markedly with decreasingMg/(Mg+SFe) of the starting material at constant CaO/Al2O3.Conversely, lowering CaO/Al2O3 reduces the temperature at constantMg/(Mg+Fe) of the starting material. Temperature differencesbetween the solidi up to 200?C are observed. All solidi displaya temperature minimum reflecting the appearance of garnet. Thisminimum shifts to lower pressure with decreasing Mg/(Mg + Fe)of the starting material. The temperature of the beginning ofmelting decreases isobarically as approximately a linear functionof the mol fraction of H2O in the vapor (XH2Ov). The data alsoshow that some CO2 may dissolve in silicate melts formed bypartial melting of peridotite. Amphibole (pargasitic hornblende) is a hypersolidus mineralin all compositions, although its P/T stability field dependson bulk rock chemistry. The upper pressure stability of amphiboleis marked by the appearance of garnet. The vapor-saturated (H2O) liquidus curve for one peridotiteis between 1250? and 1300?C between 10 and 30 kb. Olivine, spinel,and orthopyroxene are either liquidus phases or co-exist immediatelybelow the temperature of the peridotite liquidus. The data suggest considerable mineralogical heterogeneity inthe oceanic upper mantle because the oceanic geotherm passesthrough the P/T band covering the appearance of garnet in variousperidotites. The variable depth to the low-velocity zone is explained byvariable aHjo conditions in the upper mantle and possibly alsoby variations in the composition of the peridotite itself. Itis suggested that komatiite in Precambrian terrane could formby direct melting of hydrous peridotite. Such melting requiresabout 1250?C compared with 1600?C which is required for drymelting. The genesis of kimberlite can be related to partial meltingof peridotite under conditions of XH2Ov = 0.5–0.25 (XCO2v= 0.5–0.75). Such activities of H2O result in meltingat depths ranging between 125 and 175 km in the mantle. Thisrange is within the minimum depth generally accepted for theformation of kimberlite.  相似文献   

12.
Spinel granulites, with or without sapphirine, occur as lensesin garnetiferous quartzofeldspathic gneisses (leptynites) nearGokavaram in the Eastern Ghats Belt, India. Spinel granulitesare mineralogically heterogeneous and six mineral associationsoccur in closely spaced domains. These are (I) spinel–quartz–cordierite,(II) spinel–quartz–cordierite–garnet–orthopyroxene–sillimanite,(III) spinel–cordierite–orthopyroxene–sillimanite,(IV) spinel–quartz–sapphirine–sillimanite–garnet,(V) spinel–quartz-sapphirine–garnet and (IV) rhombohedral(Fe–Ti) oxide–cordierite–orthopyroxene–sillimanite.Common to all the associations are a porphyroblastic garnet(containing an internal schistosify defined by biotite, sillimaniteand quartz), perthite and plagioclase. Spinel contains variableamounts of exsolved magnetite and is distinctly Zn rich in thesapphirine-absent associations. XMg in the coexisting phasesdecreases in the order cordierite–biotite–sapphirine–orthopyroxene–spinel–garnet–(Fe–Ti)oxides. Textural criteria and compositional characteristicsof the phases document several retrograde mineral reactionswhich occurred subsequent to prograde dehydration melting reactionsinvolving biotite, sillimanite, quartz, plagioclase and spinel.The following retrograde mineral reactions are deduced: (1)spinel + quartz cordierite, (2) spinel + quartz garnet + sillimanite,(3) garnet + quartz cordierite + orthopyroxene, (4) garnet+ quartz + sillimanite cordierite, (5) spinel + cordierite orthopyroxene + sillimanite, (6) spinel + sillimanite + quartz sapphirine, (7) spinel + sapphirine + quartz garnet + sillimanite,and (8) spinel + quartz sapphirine + garnet. A partial petrogeneticgrid for the system FeO–MgO–Al2O3–SiO2–K2O–H2Oat high fo2, has been constructed and the effects of ZnO andFe2O3 on this grid have been explored Combining available experimentaland natural occurrence data, the high fo2 invariant points inthe partial grid have been located in P–T space. Geothermobarometricdata and consideration of the deduced mineral reactions in thepetrogenetic grid show that the spinel granulites evolved throughan anticlockwise P–T trajectory reaching peak metamorphicconditions >9 kbar and 950C, followed by near-isobaric cooling(dT/dP = 150C/kbar). This was superimposed by an event of near-isothermaldecompression (dT/dP = 15C/kbar). The studied spinel granulites,therefore, preserve relic prograde mineral associations andreaction textures despite being metamorphosed at very high temperatures,and bear evidence of polymetamorphism. KEY WORDS: spinel granulite; Eastern Ghats; India; polymetamorphism; geothermometry; geobarometry Corresponding author  相似文献   

13.
Upper-mantle xenoliths in volcanic pipes cutting the axis ofthe Sierra Nevada batholith contain predominantly spinel-bearingperidotites (with sporadic garnet) and garnet websterites. Inspite of the enormous thickness of the Sierran crust, the Sierranupper mantle has not attained the garnet peridotite stabilityfield. The peridotites have forsteritic (Fo88–92) olivines,Cr-diopsides, Cr-spinels, and magnesian orthopyroxenes (En88–92).Their texture and compositional characteristics of the coexistingphases indicate that these are fragments of the upper mantlethat had undergone various degrees of partial fusion. The Pconditions of reequilibration and mineralogical characteristicssuggest that the partial fusion was accompanied by diapiricuprise. The REE distribution patterns are nearly chondritic.Garnet websterite xenoliths also contain magnesian and Cr-richphases. Their bulk chemical compositions are like pyroxenitecumulates. The garnet websterites from Big Creek differ fromthose occurring at Pick and Shovel in having more Fe-rich phasesand occasional hydrous minerals. The Pick and Shovel garnetwebsterites are interpreted to be pyroxene-rich, garnet-freecumulates formed by fractional crystallization of melts generatedby partial melting of subcontinental lithosphere at depth 60km. The REE abundance of these xenoliths is consistent withthis mode of origin. Presence of jadeitic clinopyroxenes andF-rich phlogopites, and the LREE- and 87Sr/86Sr-enriched characterof the garnet websterites from Big Creek may suggest their originas metasomatized upper-mantle garnet peridotites. The latestP-T conditions of equilibration of all garnet-bearing samplesshow that they lie along a nearly adiabatic gradient in therange of 900–1000 C and 18–32 kbar. An isotopically heterogeneous, old (1 b.y.) subcontinental lithosphere,characterized by high 87Sr/86Sr (0.7044–0.7082), radiogenic206Pb/204Pb (18.86–20.04), 207Pb/204Pb (15.64–15.69)and 208Pb/204Pb (38.69–39.11), and moderate 143Nd/144Nd(0.51234–0.51260; ENd–0.35 to –5.8) is consideredto be the source of these rocks. There was a fluid influx froma subducted slab carrying Ba, K, Rb, U, Th, and radiogenic Pbinto the overlying ancient lithosphere.  相似文献   

14.
The ultrahigh-temperature (UHT) metamorphism of the Napier Complex is characterized by the presence of dry mineral assemblages, the stability of which requires anhydrous conditions. Typically, the presence of the index mineral orthopyroxene in more than one lithology indicates that H2O activities were substantially low. In this study, we investigate a suite of UHT rocks comprising quartzo-feldspathic garnet gneiss, sapphirine granulite, garnet-orthopyroxene gneiss, and magnetite-quartz gneiss from Tonagh Island. High Al contents in orthopyroxene from sapphirine granulite, the presence of an equilibrium sapphirine-quartz assemblage, mesoperthite in quartzo-feldspathic garnet gneiss, and an inverted pigeonite-augite assemblage in magnetite-quartz gneiss indicate that the peak temperature conditions were higher than 1,000 °C. Petrology, mineral phase equilibria, and pressure-temperature computations presented in this study indicate that the Tonagh Island granulites experienced maximum P-T conditions of up to 9 kbar and 1,100 °C, which are comparable with previous P-T estimates for Tonagh and East Tonagh Islands. The textures and mineral reactions preserved by these UHT rocks are consistent with an isobaric cooling (IBC) history probably following an counterclockwise P-T path. We document the occurrence of very high-density CO2-rich fluid inclusions in the UHT rocks from Tonagh Island and characterize their nature, composition, and density from systematic petrographic and microthermometric studies. Our study shows the common presence of carbonic fluid inclusions entrapped within sapphirine, quartz, garnet and orthopyroxene. Analysed fluid inclusions in sapphirine, and some in garnet and quartz, were trapped during mineral growth at UHT conditions as 'primary' inclusions. The melting temperatures of fluids in most cases lie in the range of -56.3 to -57.2 °C, close to the triple point for pure CO2 (-56.6 °C). The only exceptions are fluid inclusions in magnetite-quartz gneiss, which show slight depression in their melting temperatures (-56.7 to -57.8 °C) suggesting traces of additional fluid species such as N2 in the dominantly CO2-rich fluid. Homogenization of pure CO2 inclusions in the quartzo-feldspathic garnet gneiss, sapphirine granulite, and garnet-orthopyroxene gneiss occurs into the liquid phase at temperatures in the range of -34.9 to +4.2 °C. This translates into very high CO2 densities in the range of 0.95-1.07 g/cm3. In the garnet-orthopyroxene gneiss, the composition and density of inclusions in the different minerals show systematic variation, with highest homogenization temperatures (lowest density) yielded by inclusions in garnet, as against inclusions with lowest homogenization (high density) in quartz. This could be a reflection of continued recrystallization of quartz with entrapment of late fluids along the IBC path. Very high-density CO2 inclusions in sapphirine associated with quartz in the Tonagh Island rocks provide potential evidence for the involvement of CO2-rich fluids during extreme crustal temperatures associated with UHT metamorphism. The estimated CO2 isochores for sapphirine granulite intersect the counterclockwise P-T trajectory of Tonagh Island rocks at around 6-9 kbar at 1,100 °C, which corresponds to the peak metamorphic conditions of this terrane derived from mineral phase equilibria, and the stability field of sapphirine + quartz. Therefore, we infer that CO2 was the dominant fluid species present during the peak metamorphism in Tonagh Island, and interpret that the fluid inclusions preserve traces of the synmetamorphic fluid from the UHT event. The stability of anhydrous minerals, such as orthopyroxene, in the study area might have been achieved by the lowering of H2O activity through the influx of CO2 at peak metamorphic conditions (>1,100 °C). Our microthermometric data support a counterclockwise P-T path for the Napier Complex.  相似文献   

15.
The pressure-temperature-compositional (P-T-X) dependence ofthe solubility of Al2O3 in orthopyroxene coexisting with garnethas been experimentally determined in the P-T range 5–30kilobars and 800–1200 ?C in the system FeO—MgO—Al2O3—SiO2(FMAS). These results have been extended into the CaO—FeO—MgO—Al2O3—SiO2(CFMAS) system in a further set of experiments designed to determinethe effect of the calcium content of garnet on the Al2O3 contentsof coexisting orthopyroxene at near-constant Mg/(Mg + Fe). Startingmaterials were mainly glasses of differing Mg/(Mg + Fe) or Ca/(Ca+ Mg + Fe) values, seeded with garnet and orthopyroxene of knowncomposition, but mineral mixes were also used to demonstratereversible equilibrium. Experiments were performed in a piston-cylinderapparatus using a talc/pyrex medium. Measured orthopyroxene and corrected garnet compositions werefitted by multiple and stepwise regression techniques to anequilibrium relation in the FMAS system, yielding best-fit,model-dependent parameters Goy= –5436 + 2.45T cal mol–1,and WM1FeA1= –920 cal mol–1. The volume change ofreaction, Vo, the entropy change, So970 and the enthalpy changeHo1,970, were calculated from the MAS system data of Perkinset al. (1981) and available heat capacity data for the phases.Data from CFMAS experiments were fitted to an expanded equilibriumrelation to give an estimate of the term WgaCaMg = 1900 ? 400cal/mole cation, using the other parametric values already obtainedin FMAS. The experimental data allow the development of a arnet-orthopyroxenegeobarometer applicable in FMAS and CFMAS: where This geobarometer is applicable to both pelitic and metabasicgranulites containing garnet orthopyroxene, and to garnet peridoditeand garnet pyroxenite assemblages found as xenoliths in diatremesor in peridotite massifs. It is limited, however, by the necessityof an independent temperature estimate, by errors associatedwith analysis of low Al2O3 contents in orthopyroxenes in high-pressureor low-temperature parageneses, and by uncertainties in thecomposition of garnet in equilibrium with orthopyroxene. Ananalysis of errors associated with this formulation of the geobarometersuggests that it is subject to great uncertainty at low pressuresand for Fe-rich compositions. The results of application ofthis geobarometer to natural assemblages are presented in acompanion paper.  相似文献   

16.
The Ashland pluton is a calc-alkaline plutonic complex thatintruded the western Paleozoic and Triassic belt of the KlamathMountains in late Middle Jurassic time. The pluton comprisesa series of compositionally distinct magma pulses. The oldestrocks are hornblende gabbro and two-pyroxene quartz gabbro withinitial 87Sr/86Sr = 0{dot}7044, 18O = 8{dot}7%, and REE patternswith chondrite normalized La/Lu = 7. These units were followedby a suite of tonalitic rocks (LaN/LuN = 7) and then by a suiteof K2O- and P2O5 rocks of quartz monzodioritic affinity (LaN/LuN= 13–21; LaN/SmN = 2{dot}4–3{dot}) The quartz monzodioriticrocks were then intruded by biotite granodiorite and granitewith lower REE abundances but more fractionated LREE(LaN/LuN= 13–19; LaN/SmN = 4{dot}3–6 and they, in turn,were host to dikes and bosses of hornblende diorite. The latestintrusive activity consisted of aplitic and granitic dikes.Combined phase equilibria and mineral composition data, indicateemplacement conditions of approximately Ptotal = 2{dot}3kb,PH2O between 1{dot}5 and 2{dot}2 kb, and fO2 between the nickel-nickeloxide and hematite-magnetite buffers. Successive pulses of magma display increasing SiO2 togetherwith increasing 18O and decreasing initial 87Sr/86Sr. The isotopicdata are consistent with either (1) combined fractional crystallizationof andesitic magma and concurrent assimilation of crustal materialcharacterized by low Sr1 and high (18O or, more probably, (2)a series of partial melting events in which sources were successivelyless radiogenic but richer in 18O Each intrusive stage displaysevidence for some degree of crystal accumulation and/or fractionalcrystallization but neither process adequately accounts fortheir compositional differences. Consequently, each stage appearsto represent a distinct partial melting or assimilation event. The P2O5-rich nature of the quartz monzodiorite suite suggestsaccumulation of apatite. However, the suite contains abundantmafic microgranitoid enclaves and most apatite in the suiteis acicular. These observations suggest that magma mixing affectedthe compositional variation of the quartz monzodiorite suite.Mass balance calculations are consistent with a simple mixingprocess in which P2O5-rich alkalic basalt magma (representedby the mafic microgranitoid enclaves) was combined with a crystal-poorfelsic magma (represented by the tonalite suite), yielding aquartz monzodioritic magma that then underwent differentiationby crystal fractionation and accumulation.  相似文献   

17.
We present results of dehydration melting experiments [3–15kbar, 810–950C f(O2) QFM (quartz-fayalite-magetite)and Ni-NiO] on two Fe-rich mixtures of biotite (37%), plagioclaseAn38 (27%), quartz (34%) and ilmenite (2%), which differ onlyin their biotite compositions (mg-number 23 and 0.4). Dehydrationmelting of metagreywackes of constant modal composition generatesa wide range of melt fractions, melt compositions and residualassemblages, through the combined effects of pressure, Fe/Mgratio and f(O2). Crystallization of garnet is the chief controlon melting behavior, and is limited by two reactions: (1) thebreakdown of garnet + quartz to orthopyroxene + plagioclaseat low P, and (2) the oxidation of garnet to magnetite + anorthite+ quartz (enstatite), which is sensitive to both f(O2) andP. Because of these reactions, melting of Mg-rich metagreywackesis rather insensitive to f(O2) but strongly sensitive to P;the converse is true for Fe-rich metagreywackes. Garnet crystallizationrequires that plagioclase break down incongruently, liberatingalbite. This increases the Na2O content of the melts and enhancesmelt production. Thus, melting of metagreywacke in a reducingdeep-crustal environment (with garnet stable) would producemore, and more sodic, melt than would garnet-absent meltingof the same source material in a relatively oxidizing, shallow-crustalenvironment. KEY WORDS: anatexis; metasediments; gneisses; granites; garnet *Corresponding author. Telephone: 706-542-2394; fax: 706-542-2425; e-mail: alpatino{at}uga.cc.uga.edu  相似文献   

18.
The spinel lherzolite massif at Balmuccia, northwest Italy,forms an elongate north-south trending lens (4.5 x 0.5 x 1.1km) within the pre-Alpine granulite basement complex of theIvrea zone. The western contact is a mylonite fault zone formedduring late emplacement cataclastic flow near the Insubric line;to the east the lherzolite massif is separated from the granulitesby a magmatic sheath of layered pyroxenites, pyroxene pegmatitesand meta-gabbros. Pyroxene reaction zones on gabbro dikes indunite pods which lie east of the main lherzolite massif showthat emplacement occurred at pressures >9 kb, based on peridotiteequilibria studies. Phase chemistry calculations on pyroxenitesand granulites show ambient P–T conditions to have been850 °C (Cpx–Opx equilibria) and 10–13 kb (Opx–Gt;Plg–Gt–Sill–Qtz) during emplacement of thelherzolite massif. Temperature calculations on 12 peridotitesfrom throughout the massif suggest an earlier high-T stage (1200°C; Ol–Px–Sp) followed by partial re-equilibrationat lower T (850–950 °C; Cpx–Opx). The areaswithin the lherzolite massif with the highest calculated Ol–Px–Sptemperatures have the lowest Cpx–Opx temperatures, suggestingthat the apparent Cpx–Opx temperatures are due to re-equilibrationduring emplacement. The spinel lherzolite probably originatedat 12 and 20 kb, based on the mineral assemblage Ol + Opx +Cpx + Sp + Hnbd. The inferred P–T ranges put both themassif and the granulites on a geotherm that is high for continentalcrust and implies a high surface heat flow at the time of emplacement(2.2 µcal/cm2 sec). The Balmuccia area later became thelocus of early Mesozoic rifting between the North and SouthAlpine plates. These relationships at Balmuccia are similarto the Great Basin of the western United States, where mantlexenoliths in young basalts that show P–T conditions of1100–1300 °C at 17–20 kb, occur in an area ofhigh heat flow (2.0 µCal/cm2 sec average) and extension.This suggests an association between up-welling of mantle peridotitesbelow continents and ensialic tensional tectonics.  相似文献   

19.
A new thermobarometer, based on the equilibrium: has been calibrated with experiments carried out in the piston-cylinderapparatus. Reversed equilibria were obtained using well-calibrated2.54 cm NaCl furnace assemblies and Ag80Pd20capsules with fO2bufferedat or near iron-wustite. The equilibrium is located between5.2–5.4, 6.6–6.8, and 8.6–8.8 kb at 880, 940,and 1020?C, respectively, and at 5.2 and 8.8 kb between 865–880and 1020–1030?C, respectively. X-ray refinement data indicate that the hercynite (a = 8.15546?) has approximately 18 per cent inverse character. M?ssbauerspectra reveal that 4 mol per cent of the Fe is ferric (2 percent magnetite component). Broad Mossbauer lines and a Fe2+energy level splitting of 3.7 kJ mol–1 calculated fromthe Mossbauer spectra are consistent with the X-ray determineddegree of inversion, although no separate octahedral Fe2+ spectraldoublet is resolved. Calibration of this equation allows calculation of the equilibrium: Thermobarometers based on the above equilibria are widely applicablein granulite fades rocks and yield pressure/temperature datathat are consistent with other well-calibrated barometers andthermometers.  相似文献   

20.
Garnet-rich xenoliths in a Tertiary dike in the eastern MojaveDesert, California, preserve information about the nature andhistory of the lower crust. These xenoliths record pressuresof 10–12 kbar and temperatures of 750–800C. Approximately25% have mafic compositions and bear hornblende + plagioclase+ clinopyroxene + quartz in addition to garnet. The remainder,all of which contain quartz, include quartzose, quartzofeldspathic,and aluminous (kyanitesillimanite-bearing) varieties. Mostxenoliths have identifiable protoliths—mafic from intermediateor mafic igneous rocks, quartzose from quartz-rich sedimentaryrocks, aluminous from Al-rich graywackes or pelites, and quartzofeldspathicfrom feldspathic sediments and/or intermediate to felsic igneousrocks. However, many have unusual chemical compositions characterizedby high FeO(t), FeO(t)/MgO, Al2O3, and Al2O3/CaO, which correspondto high garnet abundance. The mineralogy and major-and trace-elementcompositions are consistent with the interpretation that thexenoliths are the garnet-rich residues of high-pressure crustalmelting, from which granitic melt was extracted. High 87Sr/86Srand low 143Nd/144Nd, together with highly discordant zirconsfrom a single sample with Pb/Pb ages of 1.7 Ga, demonstratethat the crustal material represented by the xenoliths is atleast as old as Early Proterozoic. This supracrustal-bearinglithologic assemblage may have been emplaced in the lower crustduring either Proterozoic or Mesozoic orogenesis, but Sr andNd model ages> 4 Ga require late Phanerozoic modificationof parent/daughter ratios, presumably during the anatectic event.Pressures of equilibration indicate that peak metamorphism andmelting occurred before the Mojave crust had thinned to itscurrent thickness of <30 km. The compositions of the xenolithssuggest that the lower crust here is grossly similar to estimatedworld-wide lower-crustal compositions in terms of silica andmafic content; however, it is considerably more peraluminous,has a lower mg-number, and is distinctive in some trace elementconcentrations, reflecting its strong metasedimentary and restiticheritage. * Author to whom correspondence should be addressed. Present address: Rensselaer Polytechnic Institute, Department of Earth and Environmental Sciences, Troy, New York 12180, USA. Fax: 518–276–8627; email: hanchj{at}rpi.edu.  相似文献   

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