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Boulders of the assemblage ruby—sapphire corundum, chromianmuscovite, margarite, tourmaline (chromian chlorite, Zn—Mnchromite and Mn—Ti magnetite) occur in glacial moraineand rivers of north Westland, South Island of New Zealand. Thelocation, Cr-rich composition of the boulders and the presenceof rare serpentinite rinds indicate that they are derived fromultramafic rocks (Pounamu Ultramafics) that occur within AlpineSchist of the Southern Alps. The largest sample is progressivelyzoned outwards from a corundum—margarite core, throughan intermediate zone of Cr-muscovite, to an outer zone of Cr-chloritethat is in contact with serpentinite. Most finds consist oferosion-resistant corundum-rich cores. In the corundum, Cr2O3content ranges from 0.5 to 13%, with red coloration becomingmore intense with increasing Cr. In addition to the dominantCr3+ Al3+ substitution, those of (Fe, V)3+ Cr3+ and (Ti4++Fe2+) 2Cr3+ result in spectacular colour zoning from colourlessto deep ruby red-carmine and pale blue to dark blue—violet.Corundum has grown by replacement of the micaceous matrix thatconsists of chromian muscovite (0.10–4.10% Cr2O3) andchromian margarite (0.46–1.20% Cr2O3). Both micas containa significant paragonite component (up to 21.5% in muscoviteand up to 40.8% in margarite). Late phase muscovite is Ba richwith up to 4.77% BaO, and margarite has up to 0.66% SrO. Tourmalineoccurs as veins, vein outgrowths and larger poikilitic crystalsthat replace the mica matrix. Chromium content ranges between0.82 and 3.6% Cr2O3. High bulk rock Al (up to 78% Al2O3), K,Ca, Cr and Na, and low Si (14.5–23.1% SiO2), suggest thatthe corundum—Cr-silicate rocks are the products of extrememetasomatic alteration of quartzofeldspathic schist enclavesin serpentinite. Isocon analysis indicates that conversion ofthe schist to the micaceous matrix of the corundum rocks involvesconservation of Ca, Al, K, volatiles and Sr, a mass loss of59% and a volume reduction of 69% consequent on removal of 70–80%Si and all other elements (most >80%), with enrichment ofbetween 900 and 1800% Cr. The formation of corundum from themica matrix involved a further mass—volume reduction anddecrements in Si, Ca, K, volatiles and Sr from reaction sites.Concentric mineral zonation in single rock samples and zoning—replacementin minerals, e.g. Cr in corundum and chromite, Ti, Fe2+ in corundum,Ba in muscovite, Sr in margarite, and Mn and Zn in chromiteand magnetite, imply element redistribution during metasomatism.Experimental reaction between quartzofeldspathic schist andserpentinite at 450C and 2 kbar produced reaction sequencescontaining newly formed Ca-plagioclase—phlogopitic micachloriteand muscovite—chlorite that in terms of composition areanalogous with the observed (corundum—margarite)—muscovite—chloritezonation. The temperature of metamorphism of garnet zone rocks(45020C) that contain the corundum—Cr-silicate rocksis well below that of the breakdown of muscovite and margariteto form corundum and indicates the importance of fluid composition,particularly the cation—hydrogen variables aCa2+/H+, aK+/H+and aS1O2. Introduction of boron into the schist (from serpentinite),and boron released from the breakdown of original tourmalinein the schist, resulted in tourmaline veining and reaction ofthe mica matrix to form tourmaline that invoved both a massand volume increase and addition of Fe, Mg together with B. KEY WORDS: corundum—Cr-silicate rocks; metasomatism; New Zealand; Southern Alps
*Corresponding author. 相似文献
2.
Plagioclase compositions vary from An0.1–2.5 to An32 with increasing grade in chlorite zone to oligoclase zone quartzofeldspathic schists, Franz Josef-Fox Glacier area, Southern Alps, New Zealand. This change is interrupted by the peristerite composition gap in rocks transitional between greenschist and amphibolite facies grade. Oligoclase (An20-24) and albite (An0.1–0.5) are found in biotite zone schists below the garnet isograd. With increasing grade, the plagioclase compositions outline the peristerite gap, which is asymmetric and narrows to compositions of An12 and An6 near the top of the garnet zone. In any one sample, oligoclase is the stable mineral in mica-rich layers above the garnet isograd, whereas albite and oligoclase exist in apparent textural equilibrium in adjacent quartz-plagioclase layers. The initial appearance of oligoclase in both layers results from the breakdown of epidote and possibly sphene. Carbonate is restricted to the quartz-plagioclase rich layers and probably accounts for the more sodic composition of oligoclase in these layers. The formation of more Ca-rich albite and more Na-rich oligoclase near the upper limit of the garnet zone coincides with the disappearance of carbonate and closure of the peristerite gap. Garnet appears to have only a localized effect on Ca-enrichment of plagioclase in mica-rich layers within the garnet zone. The Na-content of white mica increases sympathetically with increasing Ca-content of oligoclase and metamorphic grade. Comparison of the peristerite gap in the Franz Josef-Fox Glacier schists and schists of the same bulk composition in the Haast River area, 80 km to the S, indicates that oligoclase appears and epidote disappears at lower temperatures, and that the composition gap between coexisting albite and oligoclase is narrower in the Franz Josef-Fox Glacier area. It is suggested that a higher thermal gradient (38-40°C/km) and variations in Si/Al ordering during growth of the plagioclases between the two areas may account for these differences. In the Alpine schists the peristerite gap exists over a temperature and pressure interval of about 370-515°C and 5.5-7 kbar (550-700 MPa) PH2O. 相似文献
3.
Geothermometry and geobarometry of 10 garnet–oligoclase zone schists in the Franz Josef–Fox Glacier area, Southern Alps, New Zealand, give temperatures ranging from 415 to 625°C and pressures from 5.2 to 9.2 kbar, indicating a T–P array of about 50°C/kbar and inferred peak temperature conditions over a c. 15-km-thick section at depths between c. 20 and 34 km. The present-day distribution of the schist samples implies that only about one-third of the original crustal section is now exposed.
The garnet–oligoclase zone schists represent the deeper part of a metamorphosed and deformed accretionary complex that was associated with late Palaeozoic–early Mesozoic subduction along the Gondwana continental margin. Partial uplift ( c. 0.2 m/Ma) and erosion of the complex during Jurassic–Cretaceous times (Rangitata uplift) was synchronous with D2 deformation and recrystallization, as recorded by the P–T array. Cenozoic (Kaikoura) uplift and exhumation of the schist since c. 30 Ma to form the Southern Alps was associated with oblique-slip movement on the Alpine Fault. The present-day position and steep eastward dip of isograds and D2 structures suggest considerable clockwise rotation during uplift associated with ductile attenuation and tectonic thinning by over two-thirds of the original schist sequence, largely due to simple shear along schistosity planes. As the schist generally shows only incipient greenschist facies retrograde recrystallization, an apparently complete (although contracted) prograde mineral sequence has been preserved by rapid uplift (>5 km/Ma) of hot rock and the effects of limited shear heating near the Alpine Fault. 相似文献
The garnet–oligoclase zone schists represent the deeper part of a metamorphosed and deformed accretionary complex that was associated with late Palaeozoic–early Mesozoic subduction along the Gondwana continental margin. Partial uplift ( c. 0.2 m/Ma) and erosion of the complex during Jurassic–Cretaceous times (Rangitata uplift) was synchronous with D2 deformation and recrystallization, as recorded by the P–T array. Cenozoic (Kaikoura) uplift and exhumation of the schist since c. 30 Ma to form the Southern Alps was associated with oblique-slip movement on the Alpine Fault. The present-day position and steep eastward dip of isograds and D2 structures suggest considerable clockwise rotation during uplift associated with ductile attenuation and tectonic thinning by over two-thirds of the original schist sequence, largely due to simple shear along schistosity planes. As the schist generally shows only incipient greenschist facies retrograde recrystallization, an apparently complete (although contracted) prograde mineral sequence has been preserved by rapid uplift (>5 km/Ma) of hot rock and the effects of limited shear heating near the Alpine Fault. 相似文献
4.
Blue Mountain is a central-type alkali ultrabasic-gabbro ringcomplex (1?1?5 km) introducing Upper Jurassic sediments, Marlborough,New Zealand. The ultrabasic-gabbroic rocks contain lenses ofkaersutite pegmatite and sodic syenite pegmatite and are intrudedby ring dykes of titanaugite-ilmenite gabbro and lamprophyre.The margin of the intrusion is defined by a ring dyke of alkaligabbro. The plutonic rocks are cut by a swarm of hornblende-biotite-richlamprophyre dykes. Thermal metamorphism has converted the sedimentsto a hornfels ranging in grade from the albite-epidote hornfelsfacies to the upper limit of the hornblende hornfels facies. The rocks are nepheline normative and consist of olivine (Fo82-74),endiopside (Ca45Mg48Fe7-Ca36Mg55Fe9), titanaugite (Ca40Mg50Fe10-Ca44Mg39Fe17),plagioclase (An73-18), and ilmenitetitaniferous magnetite, withvarious amounts of titaniferous hornblende and titanbiotite.There is a complete gradation between end-iopside and titanaugitewith the coupled substitution Ry+z+Si(Ti+4+Fe+3)+Al+3 and asympathetic increase in CaAl2SiO6 (0?2-10?2 percent) and CaTiAl2O6(2?1-8?1 per cent) with fractionation. Endiopside shows a small,progressive Mg enrichment along a trend subparallel to the CaMgSi2O6-Mg2Si2O6boundary, and titanaugite is enriched in Ca and Fe+2+Fe+3 withdifferentiation. Oscillatory zoning between endiopside and titanaugiteis common. Exsolved ilmenite needles occur in the most Fe-richtitanaugites. The amphiboles show the trend: titaniferous hornblende(1?0–5?7 per cent TiO2)kaersutite (6?4 per cent TiO2)Fe-richhastingsite (18?0–19?1 per cent FeO as total Fe). Biotiteis high in TiO2 (6?6–7?8 per cent). Ilmenite and titaniferousmagnetite (3?5–10?6 per cent TiO2) are typically homogeneousgrains; their composition can be expressed in terms of R+2RO3:R+2O:R2+3O4. The intrusion of igneous rocks was probably controlled by subterraneanring fracturing. Subsidence of the country rock within the ringfracture provided space for periodic injections of magma froma lower reservoir up the initial ring fracture to form the BlueMountain rocks at a higher level. Downward movement of the floorof the intrusion during crystallization caused inward slumpingof the cumulates which affected the textural, mineralogical,and chemical evolution of the rocks in different parts of theintrusion. The order of mineral fractionation is reflected by the chemicalvariation in the in situ ultrabasic-gabbroic rocks and the successiveintrusions of titanaugite-ilmenite gabbro and lamprophyre ringdykes, marginal alkali gabbro and lamprophyre dyke swarm. Aninitial decrease, then increase in SiO2; a steady decrease inMgO, CaO, Ni, and Cr: an initial increase, then decrease inFeO+Fe2O3, TiO2, MnO, and V; almost linear increase in Al2O3and late stage increase in alkalis and P2O3, implies fractionationof olivine and endiopside, followed by titanaugite and Fe-Tioxides, followed by plagioclase, hornblende, biotite, and apatite.Reversals in the composition of cumulus olivine and endiopsideand Solidification Index, indicate that the ultrabasic-gabbroicsequence is composed of four main injections of magma. The ultrabasic rocks crystallized under conditions of high PH2Oand fairly high, constant PO2; PH2 and PO2 increased duringthe formation of the gabbroic rocks until fracturing of thechamber roof occurred. The abundance of euhedral amphibole inthe latter injection phases suggests that amphibole accumulatedfrom a hydrous SiO2 undersaturated magma when an increase inPO2, stabilized its crystallization. Plutonic complexes similar to Blue Mountain are found withinand beneath the volcanic piles of many oceanic islands, e.g.Canaries, Reunion, and Tahiti, and those intruding thick sedimentarysequences, as at Blue Mountain, e.g. the pipe-like intrusionsof the Monteregian Hills, Quebec. 相似文献
5.
Blue Mountain is a central-type alkali ultrabasic-gabbro ringcomplex (lxl7middot;5 km) introducing Upper Jurassic sediments,Marlborough, New Zealand. The ultrabasic-gabbroic rocks containlenses of kaersutite pegmatite and sodic syenite pegmatite andare intruded by ring dykes of titanaugite-ilmenite gabbro andlamprophyre. The margin of the intrusion is defined by a ringdyke of alkali gabbro. The plutonic rocks are cut by a swarmof hornblendebiotite-rich lamprophyre dykes. Thermal metamorphismhas converted the sediments to a hornfels ranging in grade fromthe albite-epidote hornfels facies to the upper limit of thehornblende hornfels facies. The rocks are nepheline normative and consist of olivine (Fo82–74),endiopside (Ca45Mg48Fe7–Ca36Mg55Fe9), titanaugite (Ca40Mg50Fe10–Ca44Mg39Fe17),plagioclase (An73–18), and ilmenitetitaniferous magnetite,with various amounts of titaniferous hornblende and titanbiotite.There is a complete gradation between endiopside and titanaugitewith the coupled substitution Ry+2+Si;;(Ti+4+Fe+3+Al+3 and asympathetic increase in CaAl2SiO6 (0·2–10·2percent) and CaTiAl2O6 (2·1–8·1 per cent)with fractionation. Endiopside shows a small, progressive Mgenrichment along a trend subparallel to the CaMgSi2O6–Mg2Si2O6boundary, and titanaugite is enriched in Ca and Fe+2+Fe+3 withdifferentiation. Oscillatory zoning between endiopside and titanaugiteis common. Exsolved ilmenite needles occur in the most Fe-richtitanaugites. The amphiboles show the trend: titaniferous hornblende(1·0–57middot;7 per cent TiO2) kaersutite (6·4per cent TiO2) Fe-rich hastingsite (18·0–19·1per cent FeO as total Fe). Biotite is high in TiO2 (6·6–7·8per cent). Ilmenite and titaniferous magnetite (3·5–10·6per cent TiO2) are typically homogeneous grains; their compositioncan be expressed in terms of R+2RO3:R+2O:R2+3O4. The intrusion of igneous rocks was probably controlled by subterraneanring fracturing. Subsidence of the country rock within the ringfracture provided space for periodic injections of magma froma lower reservoir up the initial ring fracture to form the BlueMountain rocks at a higher level. Downward movement of the floorof the intrusion during crystallization caused inward slumpingof the cumulates which affected the textural, mineralogical,and chemical evolution of the rocks in different parts of theintrusion. The order of mineral fractionation is reflected by the chemicalvariation in the in situ ultrabasic-gabbroic rocks and the successiveintrusions of titanaugite-ilmenite gabbro and lamprophyre ringdykes, marginal alkali gabbro and lamprophyre dyke swarm. Aninitial decrease, then increase in SiO2; a steady decrease inMgO, CaO, Ni, and Cr: an initial increase, then decrease inFeO+Fe2O3, TiO2, MnO, and V; almost linear increase in A12O3and late stage increase in alkalis and P2O3, implies fractionationof olivine and endiopside, followed by titanaugite and Fe-Tioxides, followed by plagioclase, hornblende, biotite, and apatite.Reversals in the composition of cumulus olivine and endiopsideand Solidification Index, indicate that the ultrabasic-gabbroicsequence is composed of four main injections of magma. The ultrabasic rocks crystallized under conditions of high PH2Oand fairly high, constant 相似文献
6.
YOSUKE KAWACHI RODNEY H. GRAPES DOUGLAS S. COOMBS MARTIN DOWSE 《Journal of Metamorphic Geology》1983,1(4):353-372
Abstract. Pink piemontite-spessartine-bearing and grey-green spessartine-bearing manganiferous quartzose schists derived from siliceous pelagites, and green quartzofeldspathic schists, are described from the greenschist facies of the Haast Schist terrane, near Arrow Junction, western Otago. Electron microprobe data are reported for sphene, spessartine-rich garnet, manganoan epidote, piemontite, tourmaline, phengitic muscovite, chlorite, albite, haematite, rutile, manganoan calcite and chalcopyrite. Metamorphism occurred at about 6.4kbar, 400°C. Xco2 was above the quartz-rutile-calcite-sphene buffer (Xco2± 0.02) throughout the recorded metamorphic history of the piemontite schists. It dropped from above to below this critical buffering value in a spessartine-rich schist and it was close to or below the buffering value in the quartzofeldspathic schists. Production of piemontite required high fO2, believed to be inherited from MnOx in the parent pelagite. Substantial loss of O2 (e.g. minimum of 0.19% by weight in one rock) during diagenesis and/or metamorphism is inferred. In the grey-green schists this inhibited piemontite formation. Slight loss of O2 and Ca2+ accompanied minor late-stage replacement of piemontite by second generation spessartine. Observed zoning and mineral replacements indicate rise of temperature, drop in pressure, or invasion by solutions of lower fO2 and XCO2 equilibrated with surrounding schists. The detailed chemistry of the minerals studied correlates with available Mn and with bulk-rock (Fe3+ x 100)/(Fe2++ Fe3+). The oxidation ratio ranges from 24 in average green quartzofeldspathic schist, through 78 in average grey-green manganiferous quartzose schist, to almost 100 in some piemontite-bearing schists. As Fe2+ gives way to Fe3+, Mg/Fe ratios tend to rise in chlorite, phengite, tourmaline, spessartine, and calcite, Mn increases and Ti decreases in haematite, Mn increases in spessartine and calcite, and Fe increases in rutile. Available divalent cations are depleted relative to Al; chlorite is more aluminous, and phengite more paragonitic than in typical Haast schists. 相似文献
7.
Melting and Thermal Reconstitution of Pelitic Xenoliths, Wehr Volcano, East Eifel, West Germany 总被引：3，自引：0，他引：3
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
8.
The western part of the Hidaka Metamorphic Belt, Hokkaido, consistsof primary pyroxene gabbro and lesser amounts of olivine gabbrothat have been dynamically metamorphosed to metagabbro—gabbroicamphibolite-amphibolite-epidote amphibolite during uplift andshearing about 23 m.y. ago. Textures and the presence of relic and recrystallized amphiboleand plagioclase in the same rock indicate incomplete reactionand non attainment of equilibrium during recrystallization. EPMA and bulk analyses of 165 amphiboles indicate a continuousoverall compositional range from actinolite to dark green hornblende(with 100 mg/(Mg+Fe2++Fe3+Mn) ratios varying from 89.5 to 32.0)marked by increasing Al, Fe, Ti, and Na. A compositional gapis usually present between relic and recrystallized amphibolesin any one rock which becomes more prominent with increasingshearing. In addition to host rock chemical control, amphibole compositionis largely dependent on the An content of coexisting plagioclase.Locally epidote and sphene exert a strong influence on bothamphibole and plagioclase compositions. Amphibole Ti and Mncontents decrease with shearing and Fe enrichment of the hostrocks largely as a result of the incoming of rutile, sphene,and Fe-Ti oxides. Analysis of host rock oxidation ratio andamphibole compositions indicates that the rocks essentiallybehaved as closed systems to oxygen during metamorphism. Al1V-AlIV, AlIV-Fe3+, and AlIV-(Na, K)A are the main substitutionsin the amphiboles. Within any one rock the recrystallized amphibolesare enriched in Al, Fe, Ti, and Na relative to the relice amphiboles.Increasing metamorphism results in a progressive change of amphiboles(recrystallized) to more Fe and Si (rather than Al) rich compositionsreflecting the trend towards greenschist where Fe-actinolite(+Mg chlorite) would be stable. Differentiation of the amphiboles is within the limits of SiAlreplacement and the compositional limits of the early stagereaction rim and replacement amphiboles in the host olivineand pyroxene metagabbros. 相似文献
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