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1.
The early augite syenite unit in the 1·13-Ga-old Ilímaussaqintrusive complex, South Greenland, consists of a magmatic assemblageof ternary alkali feldspar + fayalitic olivine + augite + titanomagnetite+ apatite + baddeleyite ± nepheline ± quartz ±ilmenite ± zircon. Feldspar, nepheline and QUILF thermometryyield T = 1000–700°C, at P = 1 kbar, which is derivedfrom fluid inclusion data from other parts of the complex. Ternaryfeldspar was the first major liquidus phase. It crystallizedat temperatures between 950 and 1000°C from a homogeneousmagma with aSiO2 = 0·8 and fO2 about 1·5–2log units below the fayalite–magnetite–quartz (FMQ)buffer. Later, closed system fractionation produced nepheline-bearingassemblages with aSiO2 = 0·4 and log fO2 = FMQ –3 to FMQ – 5. Assimilation of wall rocks produced localvariations of melt composition. Four traverses through the unitwere sampled parallel to the assumed direction of crystallization.They exhibit significant differences in their mineral assemblagesand compositions. The chemical zoning and calculated intensiveparameters of four sample suites reflect both closed systemfractional crystallization and local assimilation of wall rocks. KEY WORDS: alkaline magmatism; assimilation; fractionation; redox equilibria; QUILF  相似文献   

2.
The Puklen complex of the Mid-Proterozoic Gardar Province, SouthGreenland, consists of various silica-saturated to quartz-bearingsyenites, which are intruded by a peralkaline granite. The primarymafic minerals in the syenites are augite ± olivine +Fe–Ti oxide + amphibole. Ternary feldspar thermometryand phase equilibria among mafic silicates yield T = 950–750°C,aSiO2 = 0·7–1 and an fO2 of 1–3 log unitsbelow the fayalite–magnetite–quartz (FMQ) bufferat 1 kbar. In the granites, the primary mafic minerals are ilmeniteand Li-bearing arfvedsonite, which crystallized at temperaturesbelow 750°C and at fO2 values around the FMQ buffer. Inboth rock types, a secondary post-magmatic assemblage overprintsthe primary magmatic phases. In syenites, primary Ca-bearingminerals are replaced by Na-rich minerals such as aegirine–augiteand albite, resulting in the release of Ca. Accordingly, secondaryminerals include ferro-actinolite, (calcite–siderite)ss,titanite and andradite in equilibrium with the Na-rich minerals.Phase equilibria indicate that formation of these minerals tookplace over a long temperature interval from near-magmatic temperaturesdown to  相似文献   

3.
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   

4.
Crystallization experiments on three comendites provide evidencefor the genetic relationships between peralkaline rhyolitesin the central Kenya rift valley. The crystallization of calcicclinopyroxene in slightly peralkaline rhyolites inhibits increasein peralkalinity by counteracting the effects of feldspar. Fractionationunder high fO2 conditions produces residual liquids that areless, or only slightly more, peralkaline than the bulk composition.In contrast, crystallization under reduced conditions (<FMQ,where FMQ is the fayalite–magnetite–quartz buffer)and at high fF2 inhibits calcic clinopyroxene and yields residualliquids that are more peralkaline than coexisting alkali feldspar,whose subsequent crystallization increases the peralkalinityof the liquid. A marginally peralkaline rhyolite [molar (Na2O+ K2O)/Al2O3 (NK/A) = 1·05] can yield a more typicallycomenditic rhyolite (NK/A = 1·28) after 95 wt % of crystallization.This comendite yields pantelleritic derivatives (NK/A >1·4)after 25 wt % crystallization. Upon further crystallization,extreme peralkaline compositions (NK/A  相似文献   

5.
Scapolite and other halogen-rich minerals (phlogopite, amphibole,apatite, titanite and clinohumite) occur in some high-pressureamphibolite facies calc-silicates and orthopyroxene-bearingrocks at Sare Sang (Sar e Sang or Sar-e-Sang), NE Afghanistan.The calc-silicates are subdivided into two groups: garnet-bearingand garnet-free, phlogopite-bearing. Besides garnet and/or phlogopite,the amphibolite facies mineral assemblages in the calc-silicatesinclude clinopyroxene, calcite, quartz and one or more of theminerals scapolite, plagioclase, K-feldspar, titanite, apatiteand rarely olivine. Orthopyroxene-bearing rocks consist of clinopyroxene,garnet, plagioclase, scapolite, amphibole, quartz, calcite andaccessory dolomite and alumosilicate (kyanite?). Retrogradephases in the rocks are plagioclase, scapolite, calcite, amphibole,sodalite, haüyne, lazurite, biotite, apatite and dolomite.The clinopyroxene is mostly diopside and rarely also hedenbergite.Aegirine and omphacite with a maximum jadeite content of 29mol % were also found. Garnet from the calc-silicates is Grs45–95Py0–2and from the orthopyroxene-bearing rocks is Grs10–15Py36–43.Peak P–T metamorphic conditions, calculated using availableexchange thermobarometers and the TWQ program, are 750°Cand 1·3–1·4 GPa. Depending on the rock type,the scapolite exhibits a wide range of composition (from EqAn= 0·07, XCl =0·99 to EqAn = 0·61, XCl =0·07).Equilibria calculated for scapolite and coexisting phases atpeak metamorphic conditions yield XCO2 = 0·03–0·15.XNaCl (fluid), obtained for scapolite, ranges between 0·04and 0·99. Partitioning of F and Cl between coexistingphases was calculated for apatite–biotite and amphibole–biotite.Fluorapatite is present in calc-silicates, but orthopyroxene-bearingrocks contain chlorapatite. Cl preferentially partitions intoamphibole with respect to biotite. All these rocks have sufferedvarious degrees of retrogression, which resulted in removalof halogens, CO2 and S. Halogen- and S-bearing minerals formedduring retrogression and metasomatism are fluorapatite, sodalite,amphibole, scapolite, clinohumite, haüyne, pyrite, andlazurite, which either form veins or replace earlier formedphases. KEY WORDS: scapolite; fluid composition; high-pressure; amphibolite facies; Western Hindukush; Afghanistan  相似文献   

6.
Both high- and medium-pressure granulites have been found asenclaves and boudins in tonalitic–trondhjemitic–granodioriticgneisses in the Hengshan Complex. Petrological evidence fromthese rocks indicates four distinct metamorphic assemblages.The early prograde assemblage (M1) is preserved only in thehigh-pressure granulites and represented by quartz and rutileinclusions within the cores of garnet porphyroblasts, and omphacitepseudomorphs that are indicated by clinopyroxene + sodic plagioclasesymplectic intergrowths. The peak assemblage (M2) consists ofclinopyroxene + garnet + sodic plagioclase + quartz ±hornblende in the high-pressure granulites and orthopyroxene+ clinopyroxene + garnet + plagioclase + quartz in the medium-pressuregranulites. Peak metamorphism was followed by near-isothermaldecompression (M3), which resulted in the development of orthopyroxene+ clinopyroxene + plagioclase symplectites and coronas surroundingembayed garnet grains, and decompression-cooling (M4), representedby hornblende + plagioclase symplectites on garnet. The THERMOCALCprogram yielded peak (M2) P–T conditions of 13·4–15·5kbar and 770–840°C for the high-pressure granulitesand 9–11 kbar and 820–870°C for the medium-pressuregranulites, based on the core compositions of garnet, matrixpyroxene and plagioclase. The P–T conditions of pyroxene+ plagioclase symplectite and corona (M3) were estimated at  相似文献   

7.
A hybrid pyroxene-bearing Weinsberg type granitoid of the SouthBohemian batholith (Austria) consists of two independent mineralassemblages that were formed during two different magmatic events.The older, inherited assemblage forms unevenly distributed millimetre-sizedmulti-grain patches of quartz + mesoperthitic alkali feldspar+ andesine/bytownite + clinopyroxene (XMg = 0·50–0·54)+ orthopyroxene (XMg = 0·35–0·42) ±ilmenite ± accessories. It is interpreted to representremnants of a mangeritic igneous rock with a superimposed granulite-faciesre-equilibration texture characterized by unzoned pyroxenesand plagioclase. The enclosing younger assemblage with alkalifeldspar + oligoclase/andesine + quartz + biotite ± accessoriescrystallized from a biotite-bearing granitic melt with feldsparsexhibiting typical magmatic zoning. Coexisting with the inheritedassemblage are zircons with a characteristic typology (S23 toD, mean J4). Zircons belonging to the granitic assemblage, onthe other hand, show a distinctly different typology (L2 toS5, mean L4) or are anhedral. A Cambrian age of formation andsubsequent re-equilibration of the inherited assemblage is inferredfrom a mean U/Pb and 207Pb/206Pb evaporation age of 523 ±5 Ma for the J4 zircons. Granitic L4 zircons show a mean 207Pb/206Pbevaporation age of 355 ± 9 Ma, interpreted as the ageof zircon growth during a Carboniferous partial melting eventin the lower crust. Granite emplacement at 345 ± 5 Mais inferred from U/Pb analysis of the anhedral zircon population.The comparably low radiogenic common Pb isotope compositionof megacrystic alkali feldspars suggests that at least somedomains of these crystals are inherited from the older, pyroxene-bearingmineral assemblage. Rb/Sr whole-rock dating is thus severelyjeopardized by the presence of the inherited alkali feldsparcrystals, leading to widely scattering data points and errorchronages of no geological significance. KEY WORDS: Austria; Bohemian Massif; geochronology; granites; Pb–Sr isotopes  相似文献   

8.
Pelitic xenoliths derived from amphibolite grade basement rocksoccur within a Pleistocene, trachytic, pyroclastic unit of theWehr volcano, East Eifel, West Germany: With increasing temperatureand/or prolonged heating at high temperature, quartz-plagioclaseand micaceous layers of the xenoliths have undergone meltingto form buchites and thermal reconstitution by dehydration reactions,melting and crystallization to form restites respectively. Thexenoliths provide detailed evidence of melting, high temperaturedecomposition of minerals, nucleation and growth of new phasesand P-T-fo2 conditions of contact metamorphism of basement rocksby the Wehr magma. Melting begins at quartz-oligoclase (An17·3Ab82·3Or0·4-An20·0Ab78·1Or1·9)grain boundaries in quartz-plagioclase rich layers and the amountof melting is controlled by H2O and alkalis released duringdehydroxylation/oxidation of associated micas. Initially, glasscompositions are heterogeneous, but with increasing degreesof melting they become more homogeneous and are similar to S-typegranitic minimum melts with SiO2 between 71 and 77 wt. per cent;A/(CNK) ratios of 1·2–1·4; Na2O < 2·95and normative corundum contents of 1·9–4·0per cent. Near micas plagioclase melts by preferential dissolutionof the NaAlSi3O8 component accompanied by a simultaneous increasein CaAl2Si2O8 (up to 20 mol. per cent An higher than the bulkplagioclase composition) at the melting edge. With increasingtemperature the end product of fractional melting is the formationand persistence of refractory bytownite (An78–80) in thosexenoliths where extensive melting has taken place. Initial stage decomposition of muscovite involves dehydroxylation(H2O and alkali loss). At higher temperatures muscovite breaksdown to mullite, sillimanite, corundum, sanidine and a peraluminousmelt. Mullite (40–43 mol. per cent SiO2) and sillimanite(49 mol. per cent SiO2) are Fe2O3 and TiO2 rich (up to 6·1–0·84and 3·6–0·24 wt. per cent respectively).Al-rich mullite (up to 77 wt. per cent Al2O3) occurs with corundumwhich has high Fe2O3 and TiO2 (up to 6·9 and 2·1wt. per cent respectively). Annealing at high temperatures andreducing conditions results in the exsolution of mullite fromsillimanite and ilmenite from corundum. Glass resulting fromthe melting of muscovite in the presence of quartz is peraluminous(A/(CNK) = 1·3) with SiO2 contents of 66–69 percent and normative corundum of 4 per cent. Sanidine (An1·9Ab26·0Or72·1-An1·3Ab15·9Or82·9)crystallized from the melt. Dehydroxylation and oxidation of biotite results in a decreaseof K2O from 8·6 to less than 1 wt. per cent and oxidetotals (less H2O + contents) from 96·5 to 88·6,exsolution of Al-magnetite, and a decrease in the Fe/(Fe + Mg)ratio from 0·41 to 0·17. Partial melting of biotitein the presence of quartz/plagioclase to pleonaste, Al-Ti magnetite,sanidine(An2·0Ab34·9Or63·1) and melt takesplace at higher temperatures. Glass in the vicinity of meltedbiotite is pale brown and highly peraluminous (A/CNK = 2·1)with up to 6 wt. per cent MgO+FeO(total iroq) and up to 10 percent normative corundum. Near liquidus biotite with higher Al2O3and TiO2 than partially melted biotite crystallized from themelt. Ti-rich biotites (up to 6 wt. per cent TiO2) occur withinthe restite layers of thermally reconstituted xenoliths. Meltingof Ti-rich biotite and sillimanite in contact with the siliceousmelt of the buchite parts of xenoliths resulted in the formationof cordierite (100 Mg/(Mg+Fe+Mn) = 76·5–69·4),Al-Ti magnetite and sanidine, and development of cordierite/quartzintergrowths into the buchite melt. Growth of sanidine enclosedrelic Ca-plagioclase to form patchy intergrowths in the restitelayers. Cordierite (100 Mg/(Mg+Fe+Mn) = 64–69), quartz,sillimanite, mullite, magnetite and ilmenite, crystallized fromthe peraluminous buchite melt. Green-brown spinels of the pleonaste-magnetite series have awide compositional variation of (mol. per cent) FeAl2O4—66·6–45·0;MgAl2O4—53·0–18·7; Fe3O4—6·9–28·1;MnAl2O4—1·2–1·5; Fe2TiO4—0·6–6·2.Rims are generally enriched in the Fe3O4 component as a resultof oxidation. Compositions of ilmenite and magnetite (single,homogeneous and composite grains) are highly variable and resultfrom varying degrees of high temperature oxidation that is associatedwith dehydroxylation of micas and melting. Oxidation mainlyresults in increasing Fe3+, Al and decreasing Ti4+, Fe2+ inilmenite, and increasing Fe2+, Ti4+ and decreasing Fe3+ in associatedmagnetite. A higher degree of oxidation is reached with exsolutionof rutile from ilmenite and formation of titanhematite and withexsolution of pleonaste from magnetite. Ti-Al rich magnetite(5·1–7·5 and 8·5–13·5wt. per cent respectively) and ilmenite crystallized from meltsin buchitic parts of the xenoliths. Chemical and mineralogic evidence indicates that even with extensivemelting the primary compositions of individual layers in thexenoliths remained unmodified. Apparently the xenoliths didnot remain long enough at high temperatures for desilicationand enrichment in Al2O3, TiO2, FeO, Fe2O3, and MgO that resultsby removal of a ‘granitic’ melt, and/or by interactionwith the magma, to occur. T °C-fo2 values calculated from unoxidized magnetite/ilmenitegive temperatures ranging from 615–710°C for contactmetamorphism and the beginning of melting, and between 873 and1054°C for the crystallization of oxides and mullite/sillimanitefrom high temperature peraluminous melts. fo2 values of metamorphismand melting were between the Ni-NiO and Fe2O3-Fe3O4 buffer curves.The relative abundance of xenolith types, geophysical evidenceand contact metamorphic mineralogy indicates that the xenolithswere derived from depths corresponding to between 2–3kb Pload = Pfluid. The xenoliths were erupted during the latestphreatomagmatic eruption from the Wehr volcano which resultedin vesiculation of melts in partially molten xenoliths causingfragmentation and disorientation of solid restite layers.  相似文献   

9.
The Diahot terrane of NE New Caledonia contains an interbeddedsequence of Cretaceous to Eocene metasediments, felsic and maficmetavolcanics that experienced c. 40 Ma high-P/T metamorphism.Metabasaltic assemblages define two prograde events (M1 andM2) and a tectonically disrupted crustal profile that extendsfrom lawsonite–blueschist conditions in the SW to paragonite–eclogiteconditions in the NE. Weakly deformed metabasalts from lowest-gradeparts of the Diahot terrane contain M1 omphacite, chlorite,lawsonite and glaucophane-bearing assemblages that partiallypseudomorph igneous plagioclase and augite, and reflect P =0·7–1·0 GPa and T = 350–400°C.M1 assemblages are enveloped by a steeply SW-dipping S2 foliationthat becomes progressively more intense towards the NE overa distance of c. 15 km. S2 assemblages are divided into fourzones: (1) lawsonite–omphacite; (2) lawsonite–clinozoisite–spessartine;(3) clinozoisite–hornblende–almandine; (4) almandine–omphacite.S2 assemblages reflect a P–T gradient that spans the exposed15 km of the Diahot terrane from P = 0·8–1·0GPa and T = 350–400°C (Zone 1) to P = 1·6–1·7GPa and T = 550–600°C (Zone 4). The systematic mineralogicalchanges reflect parts of a P–T array between 1·0and 1·7 GPa that was extensively disrupted by tectonicthinning during exhumation. KEY WORDS: blueschist; eclogite; New Caledonia; CNFMASH; pseudosection  相似文献   

10.
To model magmatic crystallization processes for mafic to intermediatecompositions at high pressure, liquidus phase relations in theforsterite–anorthite–diopside–silica (FADS)tetrahedron within the CaO–MgO–Al2O3–SiO2system have been determined at 2·0 GPa. Compositionsof five liquidus invariant points have been determined and theapproximate compositions of five others have been inferred.These involve primary phase volumes for forsterite (fo), enstatite(en), diopside (di), high quartz (qz), spinel (sp), sapphirine(sa), garnet (gt), anorthite (an), and corundum (cor). The determined(with wt % coefficients) and inferred reactions (without coefficients)that define each isobaric invariant point are as follows: 23 en + 68 di + 9 sp = 84 liq + 16 fo 37 di + 63 sa = 47 liq + 40 sp + 13 en 100 gt = 21 liq + 27 sa + 55 en + 18 di 1 di + 59 en + 41 an = 43 liq + 57 gt 18 di + 21 qz + 15 en + 47 an = 100 liq di + an + gt = liq + sa an + gt = liq + sa + en sa + an + di = liq + sp sa + an = liq + cor + sp di + cor = liq + an + sp. These phase relations provide a diverse range of constraintson igneous processes at pressures near 2 GPa. They show thatfractional crystallization of a model basalt gives a residualliquid strongly enriched in SiO2, strongly depleted in MgO,and mildly enriched in Al2O3. Such a trend is consistent withthe calc-alkaline fractionation trend observed at subductionzones, but is in disagreement with suggestions that fractionationof tholeiitic basalt in this pressure range yields an alkalicbasalt. Both trends may occur for natural basalts dependingon the Na2O content of the parental magma. Also, the data showthat the minimum pressure for the formation of cumulate eclogitesand garnet pyroxenites is about 1·8–1·9GPa. The lower limit of pressure at which sapphirine can crystallizefrom a liquid in the FADS tetrahedron is estimated to be 1·1–1·5GPa and the upper limit is >3 GPa. Sapphirine crystallizesfrom magmas intermediate in composition between basalt and andesite.Probable igneous sapphirine in mafic associations is rare, butit occurs as part of a pyroxenite xenolith from Delegate, Australia,that we suggest is a cumulate assemblage and in a sapphirinenorite at Wilson Lake, Labrador, Canada. KEY WORDS: basalt; eclogite; sapphirine; fractional crystallization  相似文献   

11.
The mid-Jurassic calcalkaline Russian Peak intrusive complex,located in the Klamath Mountains of northern California, consistsof an elliptical peridotite-to-quartz diorite suite intrudedby two plutons of granodiorite. Several techniques were usedto decipher the crystallization conditions for ultramafic rocks,quartz diorite, and granodiorite, including comparison of parageneseswith crystallization experiments, application of geothermometersand barometers, and evaluation of phase equilibria. Contactmetamorphic assemblages, hornblende barometry, and amphibolesubstitution schemes indicate that pressures of intrusion were{small tilde}3 kbar. Plagioclase and pyroxene thermometry indicateintrusion temperatures of {small tilde}1000C for quartz dioriteand 900C for granodiorite. Phase equilibrium analysis for thereaction phlogopite+quartz=K-feldspar+enstatite+H2O, coupledwith an estimate of the water-saturated quartz diorite solidus,suggests that the solidus of two-pyroxene quartz diorite wasat {small tilde}780C with a mole fraction of water of {smalltilde}0•55. The composition of granodiorite is very similarto that used in several crystallization experiments and indicatesa solidus of 70025C. Estimates of oxygen fugacity, obtainedfrom equilibrium relations of olivine, orthopyroxene, and spinelin ultramafic rocks, magnetite and ilmenite in quartz diorite,and magnetite, K-feldspar, and biotite in quartz diorite andgranodiorite are 2•1–2•5 and 1•0–1•3log units above the quartz-fayalite-magnetite (QFM) buffer forgranodiorite and quartz diorite at their respective solidustemperatures; and 1•0–4•0 log units above QFMfor ultramafic rocks and quartz diorite at subsolidus temperatures.Thus, the quartz diorite magma was hotter, drier, and slightlyreduced relative to the grandiorite magma, differences thatset important constraints on the genesis of the Russian Peakmagmas. These results also indicate that quartz diorite wasundersaturated with respect to H2O as it reached its solidus,a condition that is consistent with the absence of deutericalteration in this unit. In contrast, granodiorite shows extensivedeuteric alteration and features pegmatites, quartz pods, andradial dikes as might be expected for H2O-saturated conditions. Although calcalkaline plutonic complexes present serious difficultiesin estimating the intensive parameters of crystallization, judiciousapplication of appropriate methods may result in the successfulevaluation of the conditions of crystallization of such complexes.  相似文献   

12.
In the Ranmal migmatite complex, non-anatectic foliated graniteprotoliths can be traced to polyphase migmatites. Structural–microtexturalrelations and thermobarometry indicate that syn-deformationalsegregation–crystallization of in situ stromatic and diatexiteleucosomes occurred at 800°C and 8 kbar. The protolith,the neosome, and the mesosome comprise quartz, K-feldspar, plagioclase,hornblende, biotite, sphene, apatite, zircon, and ilmenite,but the modal mineralogy differs widely. The protolith compositionis straddled by element abundances in the leucosome and themesosome. The leucosomes are characterized by lower CaO, FeO+MgO,mg-number, TiO2 , P2O5 , Rb, Zr and total rare earth elements(REE), and higher SiO2 , K2O, Ba and Sr than the protolith andthe mesosome, whereas Na2O and Al2O3 abundances are similar.The protolith and the mesosome have negative Eu anomalies, butprotolith-normalized abundances of REE-depleted leucosomes showpositive Eu anomalies. The congruent melting reaction for leucosomeproduction is inferred to be 0·325 quartz+0·288K-feldspar+0·32 plagioclase+0·05 biotite+0·014hornblende+0·001 apatite+0·001 zircon+0·002sphene=melt. Based on the reaction, large ion lithophile element,REE and Zr abundances in model melts computed using dynamicmelting approached the measured element abundances in leucosomesfor >0·5 mass fraction of unsegregated melts withinthe mesosome. Disequilibrium-accommodated dynamic melting andequilibrium crystallization of melts led to uniform plagioclasecomposition in migmatites and REE depletion in leucosome. KEY WORDS: migmatite; REE; trace element; partial melting; P–T conditions  相似文献   

13.
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   

14.
A suite of garnetiferous amphibolites and mafic granulites occuras small boudins within layered felsic migmatite gneiss in thenorthern part of the Sausar Mobile Belt (SMB), the latter constitutingthe southern component of the Proterozoic Central Indian TectonicZone (CITZ). Although the two types of metabasites are in variousstages of retrogression, textural, compositional and phase equilibriastudies attest to four distinct metamorphic episodes. The earlyprograde stage (Mo) is represented by an inclusion assemblageof hornblende1 + ilmenite1 + plagioclase1 ± quartz andgrowth zoning preserved in garnet. The peak assemblage (M1)consists of porphyroblastic garnet + clinopyroxene ±quartz ± rutile ± hornblende in mafic granulitesand garnet + quartz + hornblende in amphibolites and stabilizedat pressure–temperature conditions of 9–10 kbarand 750–800°C and 8 kbar and 675°C, respectively.This was followed by near-isothermal decompression (M2), andpost-decompression cooling (M3) events. In mafic granulites,the former resulted in the development of early clinopyroxene2A–hornblende2A–plagioclase2Asymplectites at 8 kbar and 775°C (M2A stage), synchronouswith D2 and later anhydrous clinopyroxene2B–plagioclase2B–ilmenite2Bsymplectites and coronal assemblages at 7 kbar, 750°C (M2Bstage) and post-dating D2. In amphibolites, ilmenite + plagioclase+ quartz ± hornblende symplectites appeared during M2at 6·4 kbar and 700°C. During M3, coronal garnet+ clinopyroxene + quartz ± hornblende-bearing symplectitesin metabasic dykes and hornblende3–plagioclase3 symplectitesembaying garnet in mafic granulites were formed. P–T estimatesshow near-isobaric cooling from 7 kbar and 750°C to 6 kbarand 650°C during M3. It is argued that the decompressionin the mafic granulites is not continuous, being punctuatedby a distinct heating (prograde?) event. The latter is alsocoincident with a period of extension, marked by mafic dykeemplacement. The combined P–T path of evolution has aclockwise sense and provides evidence for a major phase of earlycontinental subduction in parts of the CITZ. This was followedby a later continent–continent collision event duringwhich granulites of the first phase became tectonically interleavedwith younger lithological units. This tectonothermal event,of possibly Grenvillian age, marks the final amalgamation ofthe North and the South Indian Blocks along the CITZ to producethe Indian subcontinent. KEY WORDS: Central Indian Tectonic Zone; clockwise P–T path; continental collision; metabasite  相似文献   

15.
Hydrothermal synthesis and investigations of stability relationsof Mg—Al pumpellyite were conducted using high-pressurecold-seal apparatus over the temperature range 250–600°C and 2–8 kb Pfluid. Mg—Al pumpellyite Ca4Al5MgSi6O21(OH)7was synthesized from partially crystalline gel mixtures of stoichiometriccomposition at 275–410 °C, 6–9 kb Pfluid, andruns of 7–90 days. Pure monomineralic synthetic Mg—Alpumpellyite has refractive index nß = 1.624 (2) andcell dimensions = 8.825 (8) Á, b = 5.875 (5) Á,c = 19.10 (1) Á, and ß = 97.39 (7)°. The high temperature assemblage of the equivalent bulk compositionconsists of clinozoisite, hydrogrossular/grossular, aluminousseptechlorite/chlorite, quartz, and H2O. Hydrogrossular wassynthesized in the presence of quartz at 8 kb from 400–500°C, and hydrogrossular + quartz are unstable with respectto grossular + H2O at 400 °C and 8 kb Pfluid. At 8 kb Pfluid,aluminous septechlorite forms at temperatures below 500 °Cwhereas aluminous 14 Á chlorite crystallizes at 500–600°C. The equilibrium relations of Mg—Al pumpellyite were determinedusing subequal mixtures of synthetic Mg—Al pumpellyiteand its high temperature assemblage. The reaction 9 Mg—Alpumpellyite = 9 clinozoisite + 6 grossular + 2 chlorite + 4quartz + 19 H2O occurs at temperatures of 390 °C at 8 kb,368 °C at 5 kb, and near 325 °C at 2 kb Pfluid. Thereversal data yield an approximate value of –3141 joules/mole°K for the standard entropy of formation for the syntheticMg—Al pumpellyite. The Schreinemakers' relations for pumpellyite, prehnite, clinozoisite,tremolite, grossular, and amesite in the presence of excessquartz and fluid were constructed in the pseudo-ternary systemCaO–Al2O3–MgO(SiO2–H2O). The results, togetherwith reconnaissance experiments on the reaction 4 Mg—Alpumpellyite + 2 quartz = 8 prehnite + aluminous septechlorite+ 2 H2O, locate the invariant point [TR] at approximately 5.7kb Pfluid and 375 °C. The results of the present study arenot compatible with previous experimental data on the invariantpoint [GR]. The P–T oriented phase relations are used to interpretsome natural parageneses developed in low-grade metabasalticrocks recrystallized under conditions of low co2. The high-temperaturestability relations of Mg—Al pumpellyite are useful todenote the onset of greenschist facies metamorphism in rocksof basaltic composition.  相似文献   

16.
Garnet-bearing assemblages of K-rich and K-poor metapelitesfrom the Ilesha Schist belt, SW Nigeria, are investigated. K-richsamples contain the assemblages (A) garnet–staurolite–muscovite–chlorite–magnetite,(B) andalusite–garnet–staurolite–muscovite–chlorite–magnetiteand (C) sillimanite–andalusite–garnet–muscovite–chlorite–magnetite.K-poor samples contain the assemblages (D) garnet–staurolite–cordierite–chloriteand (E) garnet–cordierite–chlorite ± staurolite.All assemblages contain quartz, plagioclase, biotite and ilmenite.P–T pseudosections calculated in the system CaO–Na2O–K2O–TiO2–MnO–FeO–MgO–Al2O3–SiO2 –H2O ± O2 suggest peak metamorphismat 590 ± 20°C at 5 ± 0·5 kbar, followedby retrogression to 550°C at 3·0 kbar, in agreementwith field evidence, domain assemblages, mineral compositions,modes and geothermobarometry. The absence of compositional zonationshows that garnet in all investigated rocks nucleated and grewat constant P–T–X in equilibrium with associatedminerals on the thin-section scale. However, the garnet-in reactiondid not begin until the establishment of a significant temperatureoverstep of  相似文献   

17.
Boninites are an important ‘end-member’ supra-subductionzone magmatic suite as they have the highest H2O contents andrequire the most refractory of mantle wedge sources. The pressure–temperatureconditions of boninite origins in the mantle wedge are importantto understanding subduction zone initiation and subsequent evolution.Reaction experiments at 1·5 GPa (1350–1530°C),2 GPa (1400–1600°C) and 2·5 GPa (1450–1530°C)between a model primary high-Ca boninite magma composition anda refractory harzburgite under anhydrous and H2O-undersaturatedconditions (2–3 wt % H2O in the melt) have been completed.The boninite composition was modelled on melt inclusions occurringin the most magnesian olivine phenocrysts in high-Ca boninitesfrom the Northern Tongan forearc and the Upper Pillow Lavasof the Troodos ophiolite. Direct melting experiments on a modelrefractory lherzolite and a harzburgite composition at 1·5GPa under anhydrous conditions (1400–1600°C) havealso been completed. Experiments establish a P, T ‘meltinggrid’ for refractory harzburgite at 1·5, 2 and2·5 GPa and in the presence of 2–3 wt % H2O. Theeffect of 2–3 wt % dissolved H2O produces a liquidus depressionin primary boninite of  相似文献   

18.
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   

19.
On the basis of the net transfer reactions among garnet, biotite,plagioclase and quartz (for both Mg and Fe end-member models),the garnet–biotite–plagioclase–quartz (GBPQ)geobarometer was empirically calibrated under physical conditionsof P = 1·0–11·4 kbar and T = 515–878°C,based on the input garnet–biotite temperatures and garnet–aluminosilicate–plagioclase–quartz(GASP) pressures of 224 natural aluminosilicate-bearing metapeliticsamples collated from the literature. The calibrations are internallyconsistent with the asymmetric quaternary solid solution modelof garnet, the symmetric quaternary solid solution model ofbiotite, and the Al-avoidance ternary solid solution model ofplagioclase in calibrating the garnet–biotite geothermometerand the GASP geobarometer. The resulting two GBPQ barometerformulae reproduce the input GASP pressures well within ±1·0kbar (mostly within ±0·5 kbar). For both aluminosilicate-bearingand aluminosilicate-absent metapelites, the two GBPQ barometryformulae yielded identical pressures, whether the sample wasincluded or not included in calibrating the GBPQ barometry.The random error of the GBPQ barometry may be expected as ±1·2kbar. The dP/dT slopes of these two GBPQ formulae are closeto that of the GASP barometer in P–T space. Applicationsof the GBPQ barometry of aluminosilicate-absent metapelitesto the rocks within a thermal contact aureole, or rocks withina limited geographical area without post-metamorphic structuraldiscontinuity, show no obvious pressure change. It may be concludedthat the two GBPQ barometry formulae derived in this study maybe used as practical tools for metamorphic pelites under theconditions of 515–878°C and 1·0–11·4kbar, in the composition range of Xgros >3% in garnet, Xan>17% in plagioclase, and  相似文献   

20.
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   

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