共查询到20条相似文献，搜索用时 46 毫秒
1.
Subsolidus phase relationships have been determined to pressuresof 15–27 kb for a garnet clinopyroxenite, a garnet-plagioclaseclinopyroxenite, a spinel-garnet websterite, and a two-pyroxenegranulite occurring as xenoliths in the Delegate basaltic brecciapipes. Assuming all the garnet pyroxenite suite xenoliths formedtogether or last equilibrated together, the experimental dataconstrain the P-T conditions of their formation to 13–17kb and 1050–1100 °C; for the pyroxene granulites,pressures of formation of 6–10 kb at temperatures around1100 °C are indicated. In the case of the spinel-garnetwebsterite, the texturally implied exsolution of garnet andorthopyroxene from clinopyroxene, and reaction of spinel withclinopyroxene to yield garnet, are shown to be explicable interms of approximately isobaric cooling of a pre-existing aluminousclinopyroxene+spinel aggregate. The garnet of the garnet andgarnet—plagioclase clinopyroxenites cannot, however, havebeen derived wholly by exsolution processes. New chemical data are presented for the xenoliths studied experimentallyand for several similar examples from Delegate and other easternAustralian localities. Consideration of available major andtrace element and isotopic data for garnet pyroxenite suitexenoliths from Delegate and elsewhere in the world stronglysuggests genetic relationships with their host basaltic rocks.The Delegate examples are interpreted as a series of accumulatesfrom local pockets of alkaline basaltic magma within the Earth'supper mantle, and which have subsequently undergone exsolutionand/or recrystallization in response to subsolidus cooling.A similar origin is suggested for the analogous garnet pyroxenitesfound as layers within western Mediterranean peridotite massifs.The Delegate two-pyroxene granulite xenoliths are consideredto be accidental fragments of metamorphic rocks from the deepcrust beneath eastern Australia. 相似文献
2.
Metamorphic History of Sapphirine-bearing and Related Magnesian Gneisses from Namaqualand, South Africa 总被引：1，自引：2，他引：1
Sapphirine occurs with cordierite, phlogopite, spinel, sillimanite,corundum, orthopyroxene, and gedrite in granulite facies Mg-and Al-rich paragneisses within the low P, high T NamaqualandMetamorphic Complex. The gneisses reveal a three-stage texturalhistory. Sapphirine appeared during a second stage of progrademineral growth which produced nodular structures and intergrowthsinvolving spinel, corundum, and sillimanite, pseudomorphingan earlier generation of coarse, amphibolite facies minerals.A third generation of coarse, cross-cutting, mainly hydrousminerals (gedrite, kornerupine, phlogopite) is sporadicallydeveloped. The wide variety of cofacial mineral assemblages allows thedelineation of the stable mineral associations of sapphirinein the system K2O-MgO-FeO-Al2O3-SiO2-H2O under P-T conditionsindependently estimated at about 5 kb, 750–800 °C.The natural assemblages provide constraints which, taken togetherwith existing thermodynamic and experimental data, allow theestimation of P-T slopes of sapphirine equilibria. The mineraltextures thus indicate sapphirine growth under increasing T,decreasing a(H2O), and constant or slightly increasing P. The preservation of prograde reaction textures during fine-grainedmineral growth probably results from the reduced importanceand/or more CO2-rich composition of the metamorphic fluid undergranulite facies conditions in these refractory rocks. Aqueousfluids were locally reintroduced after the metamorphic peak. 相似文献
3.
The basanite tuffs of Bullenmerri and Gnotuk maars, Victoria,enclose abundant xenoliths of spinel lherzolites, many of whichcontain amphibole ± apatite ± phlogopite. Thexenolith suite also includes cumulate wehrlites, spinel metapyroxenitesand garnet metapyroxenites. All xenolith types contain abundantlarge CO2-rich fluid inclusions. Microstructural evidence forthe exsolution of spinel, orthopyroxene, garnet and rare plagioclasefrom complex clinopyroxenes suggests that all of the metapyroxeniteshave formed from clinopyroxene (± spinel ± orthopyroxene)cumulates by exsolution and recrystallization during coolingto the ambient geotherm. Pyroxene chemistry implies that a rangeof parental magma types was involved. Garnet pyroxenites showa series of reactions to successively finer-grained, lower-Pmineral assemblages, which imply a relatively slow initial upwardtransport of the xenoliths in the magma, prior to explosiveeruption. The same process has allowed crystallization of phenocrystsfrom small patches of interstitial melt within xenoliths oflherzolite, wehrlite and metapyroxenite. Critically selected P-T estimates for 16 garnet websteritesare consistent with published experimental studies of the spinel/garnetpyroxenite transition, and define a geotherm from 900 °C,11 kb to 1100 °C, 16 kb. Other published data extend thecurve down to c. 7 kb and up to 25 kb. This elevated geothermsuggests that the high regional heat flow is related to convectiveheat transfer by dike injection accompanying the vulcanism.T estimates for the lherzolites range from 850–1050 °C;comparison with the derived geotherm implies that the spinellherzolites are derived from depths of 30–55 km. Thiszone has low seismic velocities (Vp = 6.8–7.8 km/sec)and has thus previously been regarded as a thick, largely maficlower crust. The xenolith data show that this Mower crust' isdominantly ultramafic, with layers, dikes and some large bodiesof pyroxenites and mafic granulites. The anomalously low Vpmay be due to the high T, the high proportion of fluid-filledpore volume, and the magnesian composition of the lherzolites.The seismically defined Moho (Vp >8.0 km/sec) coincides withthe experimentally determined position of the spinel lherzolite-garnetlherzolite transition. 相似文献
4.
Transition from the Zeolite to Prehnite-Pumpellyite Facies in the Karmutsen Metabasites, Vancouver Island, British Columbia 总被引：1，自引：0，他引：1
The upper Triassic Karmutsen metabasites from northeast VancouverIsland, B.C., are thermally metamorphosed by the intrusion ofthe Coast Range Batholith. The amygdaloidal metabasites developedin the outer portion of the contact aureole show a progressivemetamorphism from zeolite to prehnite-pumpellyite facies. Thesize of an equilibrium domain is extremely small for these metabasites,and the individual amygdule assemblages are assumed to be inequilibrium. Two major calcite-free assemblages (+chlorite+quartz)are characteristic: (i) laumontite+pumpellyite+epidote in thezeolite facies and (ii) prehnite+pumpellyite+epidote in theprehnite-pumpellyite facies. The assemblages and compositionsof Ca-Al silicates are chemographically and theoretically interpretedon the basis of the predicted P-T grid for the model basalticsystem, CaO-MgO-A12O3-Fe2O3-SiO2-H2O. The results indicate:(1) local equilibrium has been approached in mineral assemblagesand compositions; (2) the XFe3+ values in the coexisting Ca-Alsilicates decrease from epidote, through pumpellyite to prehnite;(3) with increasing metamorphic grade, the Fe3+ contents ofepidotes in reaction assemblages decrease in the zeolite facies,then increase in the prehnite-pumpellyite facies rocks. Suchvariations in the assemblages and mineral compositions are controlledby a sequence of continuous and discontinuous reactions, andallow delineation of T-XFe3+ relations at constant pressure.The transition from the zeolite to prehnite-pumpellyite faciesof the Karmutsen metabasites is defined by a discontinuous reaction:0·18 laumontite+pumpellyite+0·15 quartz = 1·31prehnite+ 0·78 epidote+0·2 chlorite+ 1·72H2O, where the XFe3+ values of prehnite, pumpellyite and epidoteare 0·03, 0·10 and 0·18, respectively.These values together with available thermodynamic data andour preliminary experimental data are used to calculate theP-T condition for the discontinuous reaction as P = 1·1±0·5 kb and T = 190±30°C. The effectsof pressure on the upper stability of the zeolite facies assemblagesare discussed utilizing T-XFe3+ diagrams. The stability of thelaumontite-bearing assemblages for the zeolite facies metamorphismof basaltic rocks may be defined by either continuous or discontinuousreactions depending on the imposed metamorphic field gradient.Hence, the zeolite and prehnite-pumpellyite facies transitionboundary is multivariant. 相似文献
5.
The alpine-type peridotite at Burro Mountain is a partiallyserpentinized harzburgite-dunite body approximately 2 km indiameter. It lies in a chaotic mélange derived from theFranciscan Formation (Upper Jurassic to Upper Cretaceous) ofthe southern Coast Ranges of California. The peridotite is boundedon the east by a vertical fault in the Nacimiento fault zonethat brings sedimentary rocks of Taliaferro's (1943b) AsuncionGroup (Upper Cretaceous) into contact with the peridotite. Theperidotite appears to be one of a number of tectonic lenses,having a wide range in size, that make up the mélange.These lenses include metagraywacke, metachert, greenstone, amphibolite,and blueschist, as well as ultramafic rocks, and represent awide range of pressure-temperature environments. The outer shell of the peridotite is a sheared serpentinitezone 10–15 m thick. The peridotite was tectonically emplacedat its present level as a cold solid mass and had little effecton the mineral assemblages of the Franciscan Formation. Localdevelopment of lawsonite and aragonite in shear zones may berelated to the peridotite emplacement. Foliated harzburgite forms approximately 60 per cent of theperidotite. It is a lithologically uniform rock that has anolivine: orthopyroxene ratio of approximately 75:25. Accessoryclinopyroxene and chromian spinel generally make up less than5 per cent of the harzburgite. Dunite, composed of olivine,accessory chromian spinel (< 5 per cent), and trace amountsof pyroxene, makes up approximately 40 per cent of the peridotiteand occurs as dikes, sills, and irregular bodies in the harzburgite. Olivine and pyroxene show small but significant compositionalvariations and chromian spinel shows a large range in the cationratio Cr/(Cr+Al+ Fe3+). The compositional variations in theseminerals are related to original differences in bulk chemicalcomposition. The following compositional ranges were determinedfor minerals in the harzburgite: olivine, Fo91.1–Fo91.4;orthopyroxene, En89.8–En91.1; clinopyroxene, Ca47.0Mg50.0Fe3.0–Ca48.7Mg48.2Fe3.1;chromian spinel, Cr/(Cr+Al+Fe3+) 0.37–0.55. The pyroxeneshave a range in A12O3 content of 1.3–3.0 wt per cent.Olivine from dunite ranges from Fo91 to Fo92 7 and the chromianspinel has a range in the Cr/(Cr+Al+Fe3+) ratio of 0.30–0.75.Although all the dunites are lithologically similar, three distincttypes are recognized on the basis of composition of coexistingolivine and chromian spinel. Structural relations between thethree types of dunite suggest three periods of emplacement (possiblyoverlapping) of dunite into harzburgite. The evidence indicatesthat the dunite, and probably also the harzburgite crystallizedfrom an ultramafic magma, probably in the upper mantle. After the magmatic episode and crystallization, the peridotitewas subjected to a deep-seated plastic deformation and recrystallization.The first phase of the deformation produced a pervasive, planarstructural element (S1) that crosscuts many harzburgite-dunitecontacts. It is probable that some of the dunite sills wereemplaced during this deformation. The foliation, S1, is definedby layers of different orthopyroxene content in harzburgite,and by discontinuous layers of chromian spinel in dunite. Flowor slip along S1 produced slip folds in harzburgite—dunitecontacts with axial planes parallel to S1. At a later stage,isoclinal folds developed in S1, and the present olivine microfabricwas probably formed by recrystallization in the stress fieldthat produced the isoclinal folding. In the olivine microfabric,X tends to be perpendicular to the axial planes (S2) of theisoclinal folds and Y and Z tend to form double maxima in S2approximately 90° apart. Mg–Fe2+ distribution betweencoexisting mineral pairs yields a calculated temperature offormation of approximately 1200 °C. Although this temperatureis only a nominal value, it indicates that the mineral pairsequilibrated at a significantly high temperature. In view ofthe deformation and recrystallization, the calculated temperaturepossibly represents subsolidus re-equilibration of the mineralsduring this event. The deformation and recrystallization probablyoccurred shortly after crystallization while the peridotitewas still at a high temperature. A later deep-seated deformation produced small scattered kinkfolds in S1 that tend to disrupt the major olivine microfabric.The kink folding was accompanied or followed by the developmentof kink bands in olivine that reflect intragranular glidingon the system T = [Okl], t = [100]. The kink bands probablyformed at a minimum temperature of 1000 °C. Following the deep-seated deformation, which probably took placein the mantle, the peridotite mass was tectonically detachedand moved upward to its present level in the crust. Cleavages,joints, and faults provided channels for water to pervade theperidotite and allow alteration of the primary minerals. 相似文献
6.
The stability of chloritoid, FeAl2SiO6H2O, was investigatedat fluid pressures less than 10 kb. At oxygen fugacities definedby the Ni-NiO buffer, chloritoid reacts to Fe-cordierite andhercynite spinel at 550 and 575 °C at 1 and 2 kb fluid pressure.At pressures between 2.5 and 3.5 kb the assemblage aluminousferro-anthophyllite, staurolite and hercynite spinel appears.The breakdown of chloritoid to this assemblage takes place at625, 650, and 675 °C at 5.5, 7.0, and 8.7 kb, respectively.The aluminous ferro-anthophyllite assemblage is stable onlyover 50 °C, reacting with increasing temperature to almandine,staurolite, and hercynite spinel. Under the QFM buffer, thesame equilibria are displaced to higher temperatures and thealuminous ferro-anthophyllite bearing field is further restrictedwith respect to temperature. The 7 Å chamosite assemblage,previously considered to be the metastable equivalent of chloritoidat low pressures, is shown to be unstable and chloritoid canbe synthesized at pressures as low as 1 kb. An analysis of the equilibria and related experimental datapermits the construction of a schematic P-T grid which outlinesthe stability limits of several important mineral assemblagesin this system. Although the experimental and natural systemsare not strictly analogous, there is an excellent degree ofcorrespondence between the defined upper limit of chloritoidstability and previous estimates of the facies boundaries itserves to define. 相似文献
7.
Hydrothermal investigation of the bulk composition CaO.Al2O3.4SiO2+excessH2O has been conducted using conventional techniques over thetemperature ranges 200–450 °C and 500–6000 barsPfluid. A number of reactions have been studied by employingmineral mixtures consisting of reactants and products in about9: 1 and 1: 9 ratios. The phase relations were deduced fromrelatively long experiments by observing which seeded assemblagedisappeared or decreased markedly in one of the paired run charges. Laumontite was synthesized in the laboratory, probably for thefirst time. Laumontite was grown from seeded wairakite to over99 per cent using a weak NaCl solution. The refractive indicesof the synthetic material are about = 1.504 and = 1.514. Theaverage unit cell dimensions are a0 = 14.761±0.005 Å;b0 = 13.077±0.005 Å; c0 = 7.561±0.003 Å;and ß = 112.02°±0.04°. Within the errorof measurement, the optical properties and cell parameters arein good agreement with those of natural laumontite. The equilibriumdehydration of laumontite involves two reactions: (1) laumontite= wairakite+2H2O, passing through about 230 °C at 0.5 kb,255±5 °C at 1 kb, 282±5 °C at 2 kb, 297±5°C at 3 kb and 325±5 °C at 6 kb; and (2) laumontite= lawsonite+2 quartz+2H2O, taking place at about 210 °Cat 3 kb and 275 °C at 3.2 kb. Above 300 °C, the equilibriumcurve for the solid-solid reaction (3) lawsonite+2 quartz =wairakite passes through 305 °C, 3.4 kb and 390 °C,4.4 kb. Equilibrium has been demonstrated unambiguously forthe above three reactions. The hydrothermal decomposition ofnatural laumontite above its own stability limit appears tobe a very slow process. Combined with previously published equilibria determined hydrothermallyfor wairakite, the phase relations are further investigatedby chemographic analysis interrelating the phases, laumontite,wairakite, lawsonite, anorthite, prehnite+kaolinite, and 2 pumpellyite+kaolinitein the system CaAl2Si2O8-SiO2-H2O. This synthesis allowed theconstruction of a semiquantitative petrogenetic grid applicableto natural parageneses and the delineation of the physical conditionsfor the various low-grade metamorphic facies in low µCO2environments. The similar stratigraphic zonations, consistentlyfound in a variety of environments, are recognized to be a functionof burial depth, geothermal gradient, and mineralogical andchemical composition of the parental rocks. Departures fromthe normal sequences are believed to be due to the combinationsof mineralogical variations, availability of H2O, differencesin the ratio µCO2/µH2O, and the rate of reaction.The possible P-T boundaries for diagenesis, the zeolite facies,the lawsonite-albite facies, the prehnite-pumpellyite facies,and the adjacent metamorphic facies are illustrated diagrammatically. 相似文献
8.
Origin of Pyroxenite-Peridotite Veined Mantle by Refertilization Reactions: Evidence from the Ronda Peridotite (Southern Spain) 总被引：4，自引：0，他引：4
Bodinier Jean-Louis; Garrido Carlos J.; Chanefo Ingrid; Bruguier Olivier; Gervilla Fernando 《Journal of Petrology》2008,49(5):999-1025
The Ronda orogenic peridotite (southern Spain) contains a varietyof pyroxene-rich rocks ranging from high-pressure garnet granulitesand pyroxenites to low-pressure plagioclase–spinel websterites.The ‘asthenospherized’ part of the Ronda peridotitecontains abundant layered websterites (‘group C’pyroxenites), without significant deformation, that occur asswarms of layers showing gradual modal transitions towards theirhost peridotites. Previous studies have suggested that theselayered pyroxenites formed by the replacement of refractoryspinel peridotites. Here, we present a major- and trace-element,and numerical modelling study of a layered outcrop of groupC pyroxenite near the locality of Tolox aimed at constrainingthe origin of these pyroxenites after host peridotites by pervasivepyroxene-producing, refertilization melt–rock reactions.Mg-number [= Mg/(Mg + Fe) cationic ratio] numerical modellingshows that decreasing Mg-number with increasing pyroxene proportion,characteristic of Ronda group C pyroxenites, can be accountedfor by a melt-consuming reaction resulting in the formationof mildly evolved, relatively low Mg-number melts (0·65)provided that the melt fraction during reaction and the time-integratedmelt/rock ratio are high enough (>0·1 and > 1,respectively) to balance Mg–Fe buffering by peridotiteminerals. This implies strong melt focusing caused by melt channellingin high-porosity domains resulting from compaction processesin a partial melted lithospheric domain below a solidus isothermrepresented by the Ronda peridotite recrystallization front.The chondrite-normalized rare earth element (REE) patterns ofgroup C whole-rocks and clinopyroxenes are convex-upward. Numericalmodeling of REE variations in clinopyroxene produced by a pyroxene-forming,melt-consuming reaction results in curved trajectories in the(Ce/Nd)N vs (Sm/Yb)N diagram (where N indicates chondrite normalized).Based on (Ce/Nd)N values, two transient, enriched domains betweenthe light REE (LREE)-depleted composition of the initial peridotiteand that of the infiltrated melt may be distinguished in thereaction column: (1) a lower domain characterized by convex-upwardREE patterns similar to those observed in Ronda group C pyroxenite–peridotite;(2) an upper domain characterized by melts with strongly LREE-enrichedcompositions. The latter are probably volatile-rich, small-volumemelt fractions residual after the refertilization reactionsthat generated group C pyroxenites, which migrated throughoutthe massif—including the unmelted lithospheric spinel-tectonitedomain. The Ronda mantle domains affected by pyroxenite- anddunite- or harzburgite-forming reactions (the ‘layeredgranular’ subdomain and ‘plagioclase-tectonite’domain) are on average more fertile than the residual, ‘coarsegranular’ subdomain at the recrystallization front. Thisindicates that refertilization traces the moving boundariesof receding cooling of a thinned and partially melted subcontinentallithosphere. This refertilization process may be widespreadduring transient thinning and melting of depleted subcontinentallithospheric mantle above upwelling asthenospheric mantle. KEY WORDS: subcontinental mantle; refertilization; pyroxenite; peridotite; websterite; melt–rock reaction; plagioclase; trace elements 相似文献
9.
Solid bodies of upper-mantle peridotite, emplaced in the Betic-Rifchains of SW Spain and North Morocco, show a variety of structuresdeveloped under different metamorphic conditions. These structuresand related metamorphism reflect tectonic processes in the WestMediterranean mantle during orogeny in the Betic-Rif realm.The largest of the peridotites, the Ronda massif, has preservedthree structural domains which are spatially associated withmetamorphic domains previously defined by Obata (Journal ofPetrology, 21,533–572, 1980). These structural domainsinclude: (1) porphyroclastic spinel peridotites (spinel tectonites)and mylonitic garnet-spinel peridotites (garnet-spinel mylonites),developed during progressive strain localization at ambientconditions changing from the Arigite subfacies to garnet peridotitefacies; (2) seemingly undeformed granular peridotites, developedduring a phase of extensive recrystallization affecting thespinel tectonites and garnet-spinel mylonites at Seiland subfaciesconditions, and separated from the spinel tectonites by a well-preservedrecrystallization front which forms a marked structural, metamorphicand possibly geochemical boundary probably unique to orogenicperidotites; (3) porphyroclastic plagioclase peridotites (plagioclasetectonites) developed at the expense of the granular peridotitesduring progressive shear localization allied to ductile emplacementof the Ronda massif into the crust. Our structural and microstructural data from the Ronda massifallow us to assess the relative ages of the different metamorphicfacies seen in the West Mediterranean peridotites. In orderof decreasing relative age, these are: Arigite-subfacies, garnetperidotite facies, Seiland subfacies and plagioclase peridotitefacies. In addition, the associated microstructures providesome insight into the microphysical conditions controlling thedevelopment of the different structures and, as a result, thestructural and chemical heterogeneity of the West Mediterraneanperidotites. KEY WORDS: structural geology; peridotite; Betic Cordillera; Ronda; recrystallization; strain localization
*Corresponding author. Present address: Philips Electron Optics BV, Applications Laboratory, Building AAE, PO Box 218, 5600 MD Eindhoven, The Netherlands 相似文献
10.
SELVERSTONE JANE; SPEAR FRANK S.; FRANZ GERHARD; MORTEANI GIULIO 《Journal of Petrology》1984,25(2):501-531
The hornblende garbenschist horizon of the Lower Schieferhulleseries (LSH) in the SW Tauern Window, Austria, contains theassemblage hornblende + kyanite + staurolite + garnet + biotite+ epidote + plagioclase + ankerite + quartz + rutile + ilmenite,with either chlorite or paragonite present in all samples. Theseassemblages are divariant in the system SiO2-Al2O3-TiO2-Fe2O3-MgO-FeO-MnO-CaO-Na2O-K2O-H2O-CO2.Garnet-biotite geothermometry yields temperatures of final equilibrationof {small tilde}550 °C, and garnet-plagioclase-kyanite-quartzgeobarometry indicates pressures of 6–8 kb for the matrixassemblage and 9–10 kb for plagioclase inclusions in garnet.Quantitative modelling of zoned garnet, hornblende, and plagioclaseindicates growth and equilibration along a decompression pathfrom {small tilde}530 °C, 10 kb to {small tilde}550 °C,7 kb. Fluid inclusion data constrain the uplift path to havepassed through a point at {small tilde} 375 °C, 1.5 kb. These data permit the construction of a relatively completeP-T loop for metamorphism associated with the Alpine orogeniccycle in the LSH of the SW Tauern Window. The maximum pressureconditions ({small tilde}10 kb at 530 °C) recorded alongthis loop are considerably higher than previous estimates of5–7 kb for the region. Simple overthrust models developedfor the Tauern Window cannot account for pressures of this magnitude;a more likely scenario involves partial subduction of the rocksto a depth of {small tilde}35 km, followed by prolonged heatingin response to decay of the subduction isotherms. Initial upliftappears to have been rapid and occurred along a nearly isothermalpath. Significant cooling did not occur until the rocks werewithin {small tilde}5 km of the surface. Detailed tectonic modelsfor the evolution of the Tauern Window must be able to accountfor the quantitative features of the P-T loop. 相似文献
11.
Eclogites and blueschists occur in the basement and continentalshelf deposits in the Saih Hatat tectonic window of northeasternOman, where they structurally underlie the Semail ophiolite.These eclogites and blueschists constitute part of a coherenthigh-P/T metamorphic terrain comprised of interlayered metabasites,metapelites, and quartzofeldspathic and calcareous mica schists.The metabasites record a continuous regional trend of increasingP and T from west to east, where crossite-epidote schists incentral and western Saih Hatat grade into blueschists and eclogitesat As-Sifah, allowing for the subdivision of this terrain intothree metamorphic zones. P-T conditions range from 4?5 to 5?5kb atT <340?C for zone A to >10?2 kb at 500–580?Cfor zone C. Zoning patterns of garnets, pyroxenes, and phengite, and thecompositions of pyroxene and amphibole inclusions in garnet,indicate that the eclogites and enclosing high-grade blueschistsof zone C followed a ‘clockwise’ P-T rpath of increasingP and T followed by increasing T and decreasing P and a finalstage of retrogression. Garnets and pyroxenes crystallized atdifferent stages of P-T evolution of the terrain in the variouseclogite pods and boudins. This conclusion and the contrastingmineralogies of the eclogites and the enclosing blueschistsare attributed to differences in bulk-rock chemistry, fluidavailability, or fluid compositions within the terrain. The blueschists and eclogites of this terrain formed as a resultof A-type subduction and crustal thickening of the Oman continentalmargin along an east-northeast-dipping thrust or ‘subductionzone’ which was initiated by the change in plate motionbetween Africa and Eurasia at 131 Ma. High P/T metamorphismcontinued until the final stages of ophiolite emplacement inthe late Cretaceous, as indicated by the metamorphism of thethrust sheets overlying the coherent terrain. 相似文献
12.
Garnet-peridotite stability and occurrence in crust and mantle 总被引：10，自引：0，他引：10
The boundary between the spinel- and garnet-lherzolite mineral facies is strongly curved between 1300° C and 1450° C; below 1200° C it lies almost parallel to the temperature axis of the T-P diagram.Pressure of at least 12 kb is required to stabilise garnet-peridotite on the geothermal gradient and the depth at which the boundary is encountered is not sensitive to variations in the geotherm.Garnet-peridotite is metastable with respect to spinel-peridotite in normal continental crust. Natural occurrences are mantle derived and have either suffered rapid upward transit in diatremes or, in orogenic zones, either they were emplaced after upward tectonic transport through tens of kilometres, or have originated by in situ metamorphism of pre-existing crustal peridotite in an orogenic root downfolded to depths of at least 40 km. 相似文献
13.
Jane Selverstone 《Contributions to Mineralogy and Petrology》1982,79(1):28-36
Granulite xenoliths within alkali olivine basalts of the Pali-Aike volcanic field, southern Chile, contain the mineral assemblage orthopyroxene + clinopyroxene + plagioclase + olivine + green spinel. These granulites are thought to be accidental inclusions of the lower crust incorporated in the mantle-derived basalt during its rise to the surface. Symplectic intergrowths of pyroxene and spinel developed between olivine and plagioclase imply that the reaction olivine+plagioclase = Al-orthopyroxene + Al-clinopyroxene + spinel (1) occurred during subsolidus cooling and recrystallization of a gabbroic protolith of the granulites.Examination of fluid inclusions in the granulites indicates the ubiquitous presence of an essentially pure CO2 fluid phase. Inclusions of three different parageneses have been recognized: Type I inclusions occur along exsolution lamellae in clinopyroxene and are thought to represent precipitation of structurally-bound C or CO2 during cooling of the gabbro. These are considered the most primary inclusions present. Type II inclusions occur as evenly distributed clusters not associated with any fractures. These inclusions probably represent entrapment of a free fluid phase during recrystallization of the host grains. IIa inclusions are found in granoblastic grains and have densities of 0.68–0.88 g/cm3. Higher density (=0.90–1.02 g/cm3) IIb inclusions occur only in symplectite phases. Secondary Type III CO2+glass inclusions with =0.47–0.78 g/cm3 occur along healed fractures where basalt has penetrated the xenoliths. Type III inclusions appear related to exsolution of CO2 from the host basalt during its ascent to the surface. These data suggest that CO2 is an important constituent of the lower crust under conditions of granulite facies metamorphism, indicated by Type I and II fluid inclusions, and of the mantle, as indicated by Type III inclusions.Correlation of fluid inclusion densities with P-T conditions calculated from both two-pyroxene geothermometry and reation (1) indicate emplacement of a gabbroic pluton at 1,200–1,300° C, 4–6 kb; cooling was accompanied by a slight increase in pressure due to crustal thickening, and symplectite formation occurred at 850±35° C, 5–7 kb. Capture of the xenoliths by the basalt resulted in heating of the granulites, and CO2 from the basalt was continuously entrapped by the xenoliths over the range 1,000–1,200° C, 4–6 kb. Examination of fluid inclusions of different generations can thus be used in conjunction with other petrologic data to place tight constraints on the specific P-T path followed by the granulite suite, in addition to indicating the nature of the fluid phase present at depth. 相似文献
14.
Precambrian aluminous paragneisses in the Hara Lake area of northeastern Saskatchewan are characterized by the stable association
of cordierite and garnet with either sillimanite or biotite; alkali feldspar is an important mineral of this association.
The aluminous gneisses are interlayered with pyroxene-plagioclase gneisses that contain orthopyroxene, clinopyroxene, hornblende,
and biotite. The gneisses in the study area and in the adjacent Charcoal Lake area were metamorphosed under conditions of
the granulite facies. The petrologic evidence is consistent with a first metamorphic event during which the association sillimanite-biotite
was stable, followed by a second event during which cordierite-garnet was stable. Consideration of mineral assemblages and
mineral chemistries of the aluminous gneisses in terms of experimentally established or thermodynamically derived reactions
suggests that recrystallization from the sillimanite-biotite association to cordierite-garnet took place at 680 °–750 °C and
3.2–4.4 kb. 相似文献
15.
Zoned Poikiloblastic Garnets: P-T Paths and Syn-Metamorphic Uplift through 30 km of Structural Depth, Wopmay Orogen, Canada 总被引：2，自引：0，他引：2
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
16.
Petro-tectonic Imprints in the Sapphirine Granulites from Anantagiri, Eastern Ghats Mobile Belt, India 总被引：5，自引：0，他引：5
SENGUPTA PULAK; DASGUPTA SOMNATH; BHATTACHARYA P. K.; FUKUOKA M.; CHAKRABORTI SUBRATA; BHOWMICK SANTANU 《Journal of Petrology》1990,31(5):971-996
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
- spinel+rutile+quartz+MgFe–1=sapphirine+ilmenite
- cordierite=sapphirine+quartz+MgFe–1
- sapphirine+quartz=orthopyroxene+sillimanite+MgFe–1
- orthopyroxene+sapphirine+quartz=garnet+MgFe–1
- orthopyroxene+sillimanite=garnet+quartz+MgFe–1
- orthopyroxene+sillimanite+quartz+MgFe–1=cordierite.
17.
Colin H. Donaldson 《Contributions to Mineralogy and Petrology》1978,65(4):363-377
A suite of protogranular- to porphyroclastic-textured spinel lherzolites and harzburgites from the Lower Carboniferous ankaramite vent at Calton Hill has been investigated for trends of modal variation and mineral composition and for variation in calculated bulk composition. The results indicate that the nodules are accidental xenoliths derived from a source at approximately 45 km depth and at 950 °C, i.e. within the mantle but above the Low Velocity Zone. The lherzolites and harzburgites have a complex petrogenetic history involving initital formation as residues from partial melting of peridotite; it is proposed that the residues were then admixed with veins of pyroxenite, followed by a complex series of metamorphic cycles of mineral reaction and exsolution, deformation, recrystallization and annealing and finally by rupture and incorporation in the ankaramite. During ascent to the surface chrome diopside in some nodules has undergone partial, incongruent melting to form a less sodic pyroxene and a soda-rich basalt melt. 相似文献
18.
Metamorphic P-T paths have been derived for staurolite-kyanitegrade and garnet grade rocks from the Orfordville Belt, west-centralNew Hampshire. P-T paths calculated from garnet zoning are consistentwith parageneses observed in amphibolites as determined froma petrogenetic grid derived for amphibolites. The P-T pathsfrom the staurolite-kyanite zone show a pressure maximum at6.5 to 7.5 kb and {small tilde} 500?C followed by heating anddecompression to approximately 5 kb, 580?C, and a final phaseof near isobaric cooling. The path from the garnet zone is similar,but does not show the final phase of isobaric cooling. Both nappe-stage and dome-stage folds are observed in the OrfordvilleBelt. Comparison of mesoscale structures with mineral growthindicates that the nappe stage deformation occurred near orbefore the pressure maximum and dome stage deformation tookplace along the decompression-heating path. The last phase ofnear isobaric cooling may have resulted from rapid verticalreadjustment of the Orfordville Belt. 相似文献
19.
The Mineral Chemistry of Ultramafic Xenoliths of Eastern China: Implications for Upper Mantle Composition and the Paleogeotherms 总被引：21，自引：0，他引：21
Ultramafic xenoliths of garnet lherzolite (?rare spinel), spinellherzolites, spinel harzburgites, clinopyroxenites, and clinopyroxenemegacrysts were collected from Cenozoic basalts in all partsof eastern China. From their modal composition and mineral chemistryall the xenoliths may be placed into three types representing:a fertile or more primitive mantle (garnet lherzolite and spinellherzolite), a refractory or more depleted mantle (spinel harzburgiteand dunite), and inclusions cognate with the host alkali basaltsat mantle pressures (pyroxenite and megacrysts). There are systematicdifferences between the mineral compositions of each type. Spinelshows a wide compositional range and the spinel cr-number [100Cr/(Cr + Al)] is a significant indicator of the xenolithtype. Spinel cr-number and Al2O3 of coexisting minerals (spinel,clinopyroxene, and orthopyroxene) are useful as refractory indicatorsfor spinel peridotite in that the cr-number increases and thepercentage of Al2O3 decreases with increasing degrees of melting.In garnet peridotite, however, the same functions vary withpressure, not degree of melting. According to P–T estimates,the various xenoliths were derived from a large range of depthsin the upper mantle: spinel peridotite from approximately 11to 22 kb (37–66 km), spinel/garnet lherzolite from 19to 24 kb (62–80 km), and garnet lherzolite from 24 to25 kb (79–83 km). We conclude that the uppermost mantlebeneath eastern China is heterogeneous, with a north-northeastzone of more depleted mantle lying beneath the continental marginand a more primitive mantle occurring towards the continentalinterior. 相似文献
20.
The metabasites within the Tokoro belt of eastern Hokkaido,Japan, suffered pervasive high–P/ Tetamorphism. Mineralassemblages and compositions of more than 400 metabasites fromthe Saroma–Tokoro district were investigated. The metabasites are divided into six metamorphic zones basedon mineral assemblages. The laumontite (Lm) zone is definedby the presence of laumontite. The prehnite–pumpellyite(Pr–Pp) zone is characterized by the association of prehnite+ pumpellyite. The lawsonite–sodic. pyroxene (Lw–Napx)zone is defined by the assemblage lawsonite + pumpellyite +sodic pyroxene + chlorite. The epidote–sodic pyroxene(Ep–Napx)(1) and (2) zones are charecterized by the assemblage epidote+ pumpellyite + sodic pyroxene + chlorite. The former is characterizedby the absence of aragonite, sodic amphibole, and winchite,as well as the presence of jadeite–poor sodic pyroxene(maxJd mol% = 13), whereas these minerals occur in the Ep–Napx(2)zone, together with jadeite–rich sodic pyroxene (max.Jd mol % = 34). In the epidote–actinolite (Ep–Act)zone, the most common assemblages contain epidote+ actionolite+ pumpellyite + chlorite. The Lm zone corresponds to the zeolite facies (150–200?Cand 1–2 kb) and the Pr–Pp zone is equivalent tothe prehnite–pumpellyite facies (200–250?C and 2–2–5kb). The Ep–Napx(I) zone appears to be stable at 200–250?C and 2? 5?3?5 kb. The pressure conditions in the Lw–Napx,Ep-Napx(2), and Ep–Act zones appear to range from 5 to6 kb, and the temperatures are estimated to be 200–230,230–270, and 270–300? C, respectively. The sequenceof the metamorphic zones is charaterized by the curved P–Tpath. The stability field of pumpellyite+ sodic+ pyroxene+ chloritein Fe3+ bearing metabasites is located in the lower–temperatureand higher–pressure part of the pumpellyite–actionolitefacies. On the basis of Schreinmaker's method, the stabilityfield of the assemblage is bounded by a high–pressurereaction Pp+ Napx+ Chl+ Ab+ Qz+ H2O= Lw+ Gl, and by a high-temperaturereaction Pp Napx+ Chl+ Ab+ Qz = Ep + Gl + H2O. 相似文献