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1.
High-temperature contact metamorphism at the contact of an alpine-typeultramafic intrusion is described. Permian spilitic volcanicsand tuffs within a zone about 750 yards in width are convertedto amphibolites and pyroxene hornfelses. In the amphibolitesthe colour of the amphibole changes from green to brown-greenand finally to deep brown at the contact. Two-pyroxene hornfelsesare developed at the contact, together with wollastonite, grossular,and hydrogrossular. Chemical changes in the amphiboles acrossthe contact aureole are: increase in (Na+ K) and (Al(6) + Fe+3+Ti) approaching the contact, and progressive decrease in thewater content. Similar chemical changes are noted in a lensof country rock included within the main ultramafic intrusion. It is considered that original high-temperature-contact effectsare often obscured by later Ca-metasomatism during serpentinizationof the ultramafic rocks, or by later tectonic deformation ofthe rocks which may involve movement of the ultramafic mass,as a relatively cold solid intrusion, to higher levels.  相似文献   

2.
Chemial analyses of twelve amphiboles from the area around Terakanambi are presented. Results indicate that they are ferro-hornblende and ferro-pargasitic hornblende types in banded iron formations; magnesio hornblende in ultramafic rocks and edenite; and ferroan pargasite and ferroan pargasitic hornblende types in calcamphibolites. Titanium content in the amphiboles of the present study is relatively low compared to results from similar zones elsewhere. The lower titanium content of the amphiboles may be attributed to either bulk chemical composition or to low oxygen fugacity. Mg/Fe ratios vary considerably and it is mainly controlled by host rock composition. The plots of calcic amphiboles on (lOONa/Ca + Na)/(100 Al/Si + Al) and Aliv/Alvi diagrams indicate that they are of medium to low pressure type.  相似文献   

3.
RAMSAY  C. R. 《Journal of Petrology》1973,14(3):467-488
Archaean meta-sediments near Yellowknife, Canada, exhibit alow-pressure facies series and broad metamorphic zonation rounda central pluton. Meta-pelites and meta-greywackes from thebiotite zone have been studied using analyses of 59 mineralsand 14 rocks. Mineral compositions were controlled by both host-rockcomposition and metamorphic grade. Increased grade commonly imposed on the minerals a progressivecompositional maturation. This involved progressive compositionalchange (especially in meta-greywacke biotites) and/or narrowingof compositional range (particularly in muscovites). Specificeffects of increased grade are as follows. Biotites in meta-greywackesexhibit increased Mg/Fe and Na/K but decreased (Na+K) content.Biotites in meta-pelites change little except for increasedAlIV/Si. The muscovites display decreasing maximum Si contents,increased AlVI at the expense of Fe and Mg, and increased Na/K.The chlorites show only a slight general increase in Mg/Fe. Bulk compositional control is manifested in various ways. Insome instances minerals from subtly different rock types areperceptibly distinct; in others the pro-grade maturation trendsof minerals in these rock types are different. Thus Si is moreabundant in meta-greywacke biotites than in meta-pelite biotitesand (Na+Ba+K) content of muscovites is greater in meta-greywackes. The observed features are used to deduce mechanisms of controlby grade and bulk composition and to discuss general circumstancesunder which they operate.  相似文献   

4.
The lower-crustal rocks of the Kohistan complex (northern Pakistan) are mostly composed of metabasic rocks such as pyroxene granulites, garnet granulites and amphibolites. We have investigated P–T trajectories of the relic two-pyroxene granulites, which are the protolith of the amphibolites within the Kamila amphibolite belt. Aluminous pyroxene retains igneous textures such as exsolution lamellae developed in the core. The significant amount of Al in clinopyroxene is buffered by breakdown reactions of plagioclase accompanied by film-like quartz as a product at grain boundaries between plagioclase and clinopyroxene. Distinct Al zoning profiles are preserved in pyroxene with exsolution lamellae in the core and in plagioclase adjacent to clinopyroxene in pyroxene granulites. In the northern part of the Kamila amphibolite belt, Al in clinopyroxene increases towards the rim and abruptly decreases at the outer rim, and anorthite in plagioclase decreases towards the rim and abruptly increases near the grain boundary between plagioclase and clinopyroxene. In the southern part of the Kamila amphibolite belt, Al in clinopyroxene and anorthite in plagioclase simply increase towards the margins of the grains. The anorthite zoning in plagioclase is in agreement with the zoning profiles of Ca-Tschermaks and jadeite components inferred from variations of Al, Na, Ti and Fe3+ in clinopyroxene. Assuming that the growth surface between them was in equilibrium, geothermobarometry based on Al zoning in clinopyroxene coexisting with plagioclase indicates that metamorphic pressures significantly increased with increasing temperature under granulite facies metamorphism. The peak of granulite facies metamorphism occurred at conditions of about 800 °C and 800–1100 MPa. These prograde P–T paths represent a crustal thickening process of the Kohistan arc during the Early to Middle Cretaceous. The crustal thickening of the Kohistan arc was caused by accretion of basaltic magma at mid-crustal depths.  相似文献   

5.
Principal components analysis is used to study the chemistry of 639 calcic amphiboles. Eigenvectors representing multiple partial correlation coefficients give various sets of substitutional relationships. The relative significance of each set can be noted by the percent variation of the data it represents. The highest percent variation (36%) is associated with the substitutions $$Si + Mg \rightleftharpoons Al^{IV} + Al^{VI} + Ti + Fe^{3 + } + Fe^{2 + } + Na + K$$ . Other expected substitutions among the ions such as AlIV + Na ? Si, the positive correlation between AlIV and AlVI etc. are shown statistically. The substitution of Al in T 1 and T 2 positions imposes an ordering in the M 1, M 2 and M 3 sites. Variability of OH in the amphiboles is found to be significant. There is no definite correlation between OH and Fe3+ but OH and Ti are positively correlated. Under certain conditions and provided the concentration of AlIV does not change significantly, Fe and Mg may be assumed to mix ideally in the amphibole solid solution.  相似文献   

6.
Four pairs of associated calcic and sodic amphiboles from blueschistfacies metamorphic rocks were analyzed with the electron microprobeand studied by single-crystal X-ray diffraction techniques.Except for ranges in the ratios Mg/(Mg+Fe) and Fe3+/(Fe3++Al+Ti),the sodic amphiboles are similar in chemical composition. Theamount of calcium in the M(4)-site ranges only from 0·18to 0·21 ion per formula unit. The calcic amphiboles,in addition to a range in Mg/(Mg+Fe), vary in Na/(Na+Ca) ratio(0·29–0·48). Three of the calcic amphibolescontain less than 1·5 calcium ions per formula unit,indicating a significant solid solution of sodic amphibole componentsin the calcic amphibole phase. The a and b unit-cell parametersof the calcic amphiboles decrease with increased content ofthe sodic component.  相似文献   

7.
Coexisting white micas and plagioclase were studied by electronmicroprobe (EMP), and transmission and analytical electron microscopy(TEM—AEM) in greenschist- to amphibolite-grade metabauxitesfrom Naxos. The TEM—AEM studies indicate that sub-micronscale (0.01–1.0 µm thick) semicoherent intergrowthsof margarite, paragonite and muscovite are common up to loweramphibolite conditions. If unrecognized, such small-scale micainterlayering can easily lead to incorrect interpretation ofEMP data. Muscovite and paragonite in M2 greenschist-grade Naxosrocks are mainly relics of an earlier high-pressure metamorphism(M1). Owing to the medium-pressure M2 event, margante occursin middle greenschist-grade metabauxites and gradually is replacedby plagioclase + corundum in amphibolite-grade metabauxites.The margarite displays minor IVAl3 VI(Fe3+, Al) Si-3 VI--1 andconsiderable (Na, K) SiCa-1Al-1 substitution, resulting in upto 44 mol% paragonite and 6 mol % muscovite in solution. Thecompositional variation of muscovite is mainly described byVI(Fe2+, Mg) Si VI Al-1VI Al-1 and VI(Fe3+Al-1) exchanges, thelatter becoming dominant at amphibolite grade, Muscovite issignificantly richer in Fe than margarite or paragonite. Ca—Na—Kpartitioning data indicate that margarite commonly has a significantlyhigher Na/(Na+ K+Ca) value than coexisting muscovite or plagioclase.Exceptions are found in several greenschist-grade rocks, inwhich M1-formed mussovite may have failed to equilibrate withM2 margarite. The sluggishness of K-rich micas to recrystallizeand adjust composidonally to changing P-T conditions is alsoreflected in the results of mus-covite-paragonite solvus thermometry.Chemical data for Ca—Na micas from this study and literaturedata indicate that naturally coexisting margarite—paragonitepairs display considerably less mutual solubility than suggestedby experimental work. The variable and irregular Na partitioningbetween margarite and muscovite as observed in many metamorphicrocks could largely be related to opposing effects of pressureon Na solubility in margarite and paragonite and/or non-equilibriumbetween micas. KEY WORDS: Ca—Na—K mica; margarite; metabauxite; Naxos; sub-micron-scale mica interlayering  相似文献   

8.
Actinolite-actinolitic hornblende and actinolitic hornblende-hornblende pairs are described from gabbroic amphibolites and epidote amphibolites formed by dynamic metamorphism during uplift of gabbroic rooks in the Hidaka Metamorphic Belt, Hokkaido. Electron microprobe analyses indicate that coupled substitutions involved in the transition from actinolite to hornblende are essentially those of edenite and tschermakite-ferritschermakite together with smaller amounts of glaucophane-riebeckite, i.e. AlIV, AlVI, Fe3+, A-site occupancy and NaM4 increase with replacement of Mg by Fe2++ Mn and Si by AlIV. During metamorphism the amount of deformation due to shearing has affected the degree of compositional discontinuity in the actinolite-hornblende series and the compositional gap is most pronounced in the epidote amphibolite. The coexisting actinolite-hornblende do not represent an equilibrium pair as textural relations indicate that the actinolitic amphiboles are relics. It is suggested that shearing deformation during uplift has caused an overstepping of the changing physico-chemical conditions of metamorphism so that compositional readjustment of amphiboles was not achieved. Equilibrium-disequilibrium actinolite-hornblende pairs are discussed from other localities where rocks of basaltic composition have been metamorphosed.  相似文献   

9.
Former idioblastic garnet crystals of an Archaean granulite with Mg/(Mg+Fe+Mn)-ratios (= M) near 0.40 were converted to symplectitic pseudomorphs consisting mainly of cordierite (M=0.61), orthopyroxene (M=0.40), and a relic garnet with a new composition (M=0.18), during a static metamorphism which is related in time to the Vredefort event. On the basis of experimental data for the continuous reaction garnet+quartz=orthopyroxene+cordierite the conditions of metamorphism were near 5 kb, 700 °C. Orthopyroxenes crystallized initially as minute, myrmekitic grains with metastable excess Al contents up to 13 mol% Al2O3 and, through grain growth and Al exsolution, transformed into dense aggregates of coarser crystals with equilibrated compositions near 3 mol% Al2O3. In the absence of free silica hercynitic spinel appears as an additional phase that coexists with cordierite, orthopyroxene, and garnet of more magnesian compositions than in the case of silica saturation.Pseudotachylite veins crosscutting the hornfelsed granulite consist of pyroxene of variable Al contents, two feldspars, opaques, and quartz, and are finely recrystallized. There is textural and mineral chemical evidence from both the Al-contents of the pyroxenes and the Mg/Fe distribution among the phases adjacent to the pseudotachylite that these veins were emplaced late during the static metamorphism, which was probably caused by a local, deep-seated magma diapir. On this basis, the meteorite impact hypothesis for the origin of the Vredefort Structure is considered less likely than a mechanism of internal origin which can be made responsible for the close link in time and space between static metamorphism and the high strain rate deformation that produced the pseudotachylite.  相似文献   

10.
Sphene is very common in rocks including albitized granite, dioritic porphyrite, calcsilicate rock and breccia from the eastern fold belt of Mount Isa Inlier, Cloncurry. Two stages of sphenes are present in these rocks. First-staged sphene is relatively fine, euhedral, some grains show round or patchy zoning; second-staged sphene is relatively large, anhedral to subhedral, some grains show patchy zoning;both possibly contain rutile, ilmenite and magnetite inclusions. All sphenes are of low-Al type. The second-staged sphene has lesser Fe apfu than the first-staged sphene. Light-color part of the sphene has bigger Fe apfu than the dark-color part, as observed on one individual grain of sphene with patchy zoning, the average Xro of the sphene with patchy zoning is greater than that of the sphene without patchy zoning. Because the sphenes are taken from different types of rocks, Si, Ti, and Al have variable relations with F OH apfu. Si and Ti are not correlated with OH F in all analyzed samples ; Fe is correlated with OH F in the sphene just from granite and dioritic porphyrite; Al is correlated with OH F in the sphene fromgranite and breccia and is not correlated with OH F in the sphene from the dioritic porphyrite and calcsilicate rocks. The first-staged sphenes were possibly formed in the processes of magmatism and metamorphism. The second-staged sphenes were formed as a result of the breakdown of hornblendes and biotites in the process of Na (Ca) -metasomatism.  相似文献   

11.
Summary The chemistry of amphiboles from schists, quartzofeldspathic gneisses and migmatites ranging in metamorphic grade from greenschist to amphibolite facies has been determined by electron microprobe. Intercalated amphibolites suggest that some of the rocks retrograded from the eclogite stability field; others were never metamorphosed above greenschist facies. Rocks which contain other mineralogical evidence for an original high pressure assemblage have amphiboles with high Na/K, low Fe and relatively low Ti. Other high-grade rocks contain amphibole of broadly pargasitic composition. The pargasites from more Ca-rich bulk compositions have less substitution of Na for Ca in the M4 site than do those from Ca-poor bulk compositions. A lower grade assemblage of amphiboles ranges from hornblende through actinolitic hornblende to actinolite; this is retrograde in the gneisses and migmatites, but may be prograde in the schists. In contrast, the high-grade assemblage shows almost constant high K with variable Na and quite different trends for edenite-type substitution (IVAl variation with A site occupancy) and variation ofIVAl with Fe/(Fe + Mg) and with Ti.
Chemische Zusammensetzung von Pargasit und Hornblende in niedrig- bis hoch-gradig metamorphen Gesteinen der Rhodope-Zone, Xanthi, Griechenland
Zusammenfassung Die Chemische Zusammensetzung von Amphibolen aus Schiefern, Quarz-Feldspat-Gneisen, und Migmatiten, deren metamorpher Grad von Grünschiefer- bis zur Amphibolitfazies reicht, wurde mit der Elektronenstrahl-Mikrosonde bestimmt. Zwischengeschaltete Amphibolite legen die Vermutung nahe, daß einige der Gesteine durch retrograde Metamorphose aus dem Eklogit-Stabilitatsfeld hervorgegangen sind; andere jedoch hatten niemals in ihrer Entwicklung einen höheren Grad als den der Grünschie-ferfazies erreicht. Gesteine, die andere mineralogische Hinweise für eine ursprungliche Hochdruck-Paragenese führen, enthalten Amphibole mit hohem Na/K, niedrigen Eisen und relativ niedrigen Ti. Andere high-grade Gesteine enthalten Amphibol von pargasitischer Zusammensetzung. Die Pargasite aus mehr Kalzium-reichen Gesteinen zeigen geringere Substitution von Natrium für Kalzium an den M4 Plätzen als jene aus Kalzium-armen Gesteinen. Eine niedriger-gradige Paragenese von Amphibolen umfaßt Zusammensetzungen von Hornblende über aktinolitische Hornblende bis zu Aktinolit; diese ist in den Gneisen und Migmatiten retrograd, durfte in den Schiefern jedoch prograd sein. Im Gegensatz dazu zeigt die hochgradige Paragenese fast durchwegs konstant hohe Kalium-Gehalte mit variablem Natrium und einen anderen Trend für Edenit-artige Substitution (IVAl Variation mit Besetzung der A Plätze) und eine Variation vonIVAl mit Fe/(Fe + Mg) und mit Ti.

With 4 Figures  相似文献   

12.
This paper attempts to illustrate the chemical variations of metamorphic hornblendes regarding host rocks and prograde variations. Changes related to bulk chemistry (orthoamphibolites) mainly concern Si, Al, Mg, Fetot and Ca. The Mg, Fe2+ and Fe3+ contents of hornblendes are, however, not strictly related to host rook compositions and Mg enrichments are correlated with increasing Fe3+ contents in the amphiboles. Thus, variations of oxygen fugacity may control the Mg contents of the Ca amphiboles studied but this does not show clear relations with the prograde metamorphism. The most sensitive but irregular variation related to the metamorphic conditions is the prograde enrichment of the alkalis into the A vacant position and an increase of the (Na+K)tot/Na+K+Ca ratios of the amphiboles. Increasing Ti and AlIV contents as well as decreasing AlVI concentrations are also, but much less evidently, related to increasing T and P. A variation trend from tschermakitic to edenitic hornblendes may be drawn using Shido's end members calculation; this tendency and the relative deficiency of AlVI contents in the low-grade members suggests that the amphiboles studied were subjected to conditions of a low-pressure metamorphism type. Such a conclusion is in agreement with the occurrence of andalusite-cordierite/sillimanite-cordierite associations in the metapelitic rocks, and the absence of Fe-rich garnet and epidote from the orthoamphibolites of the amphibolite facies at Aracena. Comparisons with Ca amphiboles from other metamorphic areas show, in agreement with various authors, that Abukuma hornblendes are similar to those encountered in high-grade thermal aureoles and tonalitic intrusives but different from the hornblendes of Barrovian metamorphism types.  相似文献   

13.
FROST  RONALD 《Journal of Petrology》1975,16(2):272-313
The 2 km wide contact aureole produced from serpentinite bythe intrusion of the Mount Stuart Batholith into the IngallsComplex at Paddy-Go-Easy Pass contains the following ultramaficassemblages, in order of increasing grade: serpentine-forsterite-diopside,serpentine-forsterite-tremolite, forsterite-talc, forsterite-anthophyllite,forsterite-enstatite-anthophyllite, forsterite-enstatite-chlorite,forsterite-enstatite-spinel. Associated metarodingites displayfive metamorphic zones, the diagnostic assemblages of whichare, in increasing grade: grossular-idocrase-chlorite, grossular-diopside-chlorite,epidote-diopside-chlorite, epidotediopside-spinel, plagioclase-grossular-diopside.Mafic hornfels in the aureole contains no orthopyroxene, indicatingthat the conditions of pyroxene hornfels facies were not reached. The breakdown of chlorite is best displayed in aluminous blackwallreaction zones around mafic inclusions in the peridotite. Attemperatures above those of the anthophyllite-out isograd, butwithin the field of forsterite+tremolite, these chlorite-richrocks react to form the assemblage: forsterite-enstatite-spinel.Calculations show that cordierite did not form as a result ofchlorite breakdown in the natural system because impurities,such as iron and chromium, displaced the equilibrium: forsterite+cordierite= enstatite+spinel to much lower pressures than the three kilobarsfound in the pure system. The primary chromite of the peridotite has been altered to chrome-magnetitein the serpentinite. This alteration seems to be isochemicalover the whole rock, as true chromite, formed by metamorphism,occurs at grades above that of the forsterite-enstatite-anthophylliteassemblage. Calcic amphibole in high-grade metaperidotite is tremolite,even in the presence of aluminous chromite, whereas that inmetamorphosed blackwall rock grades from tremolite into hornblende.The pattern of substitution appears to be: Mg2Si3rlhar2;(Na,K)(AlVI)2(AlIV)3.  相似文献   

14.
A comparison of published metabasite amphibole analyses from medium and low-pressure metamorphic terrains reveals that there is no systematic variation in Na, NaM4, Al or AlVI as a function of pressure. This may be due to blurring of the differences by variation in oxidation state, or by analytical differences between laboratories. It is not due to variable Mg/Fe in whole rocks. Differences that can be recognised are generally higher Ti/Al ratios in the low-pressure amphiboles, and a very poorly developed compositional gap between actinolite and hornblende compared with a well-developed gap at medium pressures. These features, together with the relatively low-grade appearance of calcic plagioclase at low pressures, provide the best means of distinguishing metabasites from the two facies series.All three features can be explained by the configuration of cation-exchange equilibria at the greenschist/amphibolite facies boundary. Enrichment in Ti at low-pressures is due to the positive slope of reactions partitioning Ti into the amphibole. The composition gap in amphiboles at medium-pressure is due to overstepping of the tschermakite-enriching equilibrium. At low pressures this overstepping still occurs, but the equilibrium tschermakite-content in the amphibole is much lower for a given amount of overstepping. The relatively low-grade appearance of oligoclase at low pressures is due to convergence of the tschermakite and anorthite-enriching equilibria with decreasing pressure.  相似文献   

15.
Sodic amphiboles in high pressure and ultra-high pressure (UHP) metamorphic rocks are complex solid solutions in the system Na2O–MgO–Al2O3–SiO2–H2O (NMASH) whose compositions vary with pressure and temperature. We conducted piston-cylinder experiments at 20–30?kbar and 700–800?°C to investigate the stability and compositional variations of sodic amphiboles, based on the reaction glaucophane=2jadeite+talc, by using the starting assemblage of natural glaucophane, talc and quartz, with synthetic jadeite. A close approach to equilibrium was achieved by performing compositional reversals, by evaluating compositional changes with time, and by suppressing the formation of Na-phyllosilicates. STEM observations show that the abundance of wide-chain structures in the synthetic amphiboles is low. An important feature of sodic amphibole in the NMASH system is that the assemblage jadeite–talc?±?quartz does not fix its composition at glaucophane. This is because other amphibole species such as cummingtonite (Cm), nyböite (Nyb), Al–Na-cummingtonite (Al–Na-Cm) and sodium anthophyllite (Na-Anth) are also buffered via the model reactions: 3cummingtonite?+?4quartz?+?4H2O=7talc, nyböite?+?3quartz=3jadeite?+?talc, 3Al–Na-cummingtonite + 11quartz + 2H2O=6jadeite + 5talc, and 3 sodium anthophyllite?+?13quartz?+?4H2O=3 jadeite + 7talc. We observed that at all pressures and temperatures investigated, the compositions of newly grown amphiboles deviate significantly from stoichiometric glaucophane due to varying substitutions of AlIV for Si, Mg on the M(4) site, and Na on the A-site. The deviation can be described chiefly by two compositional vectors: [NaAAlIV]<=>[□ASi] (edenite) toward nyböite, and [Na(M4)AlVI]<=>[Mg(M4)MgVI] toward cummingtonite. The extent of nyböite and cummingtonite substitution increases with temperature and decreases with pressure in the experiments. Similar compositional variations occur in sodic amphiboles from UHP rocks. The experimentally calibrated compositional changes therefore may prove useful for thermobarometric applications.  相似文献   

16.
Electron-microprobe analyses are presented for pyroxene, amphibole,and biotite from monzonite, granodiorite, and granite at Finnmarka,Norway. Compositional trends measured in biotite, present inall three rock types, and in amphibole, present in the monzoniteand granodiorite, are markedly atypical and are interpretedas reflecting crystallization under progressively more oxidizingconditions. The average Fe/Fe + Mg for biotites from successivelymore silicic rock types changes from 0.64 0.35 0.28, and foramphiboles changes from 0.58 in the monzonite to 0.29 in thegranodiorite. Analyses of selected areas within amphibole grains in the granodioriteshow marked chemical variations, although single-crystal X-rayphotographs are sharp and do not reveal multiple phases. Onthe basis of 33 such analyses, four coupled substitutions areidentified as operative; the most unusual finding is the relationof 1 Ti cation to 4 AlIV cations in the unit cell. Variationswithin individual amphibole grains of the granodiorite resemblechanges noted in evolution of amphibole composition from monzoniteto granodiorite and are interpreted as reflecting progressiveoxidation. Consideration of these data for the mafic silicates, data forthe opaque oxides, and the extensive formation of sphene inthe granodiorite, has allowed development of schematic reactionsand an overall picture of magmatic environment and evolutionat Finnmarka. Crystallization apparently took place at PH2oof 1000 bars or less and a temperature of about 700 °C.The trend of oxidation during differentiation is more extremethan any heretofore reported. Amphiboles, as well as biotites,may participate in oxidation reactions and may reflect the oxidation-reductionprocesses that occurred during magmatic evolution.  相似文献   

17.
Osamu Ujike 《Lithos》1982,15(4):281-287
A compositional gap between hypersolidus plagioclase and subsolidus plagioclase, most of which must have formed by devitrification, decreases in An % with decreasing cooling rate, probably reflecting a melt composition derived by in situ differentiation. Augitic pyroxenes, crystallized from a quickly cooling magma, tend to contain more Al, Ti, Na(+K) and Fe3+, and less Si and Mn. Compositional breaks between hypersolidus and subsolidus amphiboles with respect to the components of edenite and titanoamphibole, decrease in width with decreasing cooling rate. Subcalcic hornblende seems to grow from differentiated magmas in the course of moderate to rapid cooling.  相似文献   

18.
Abstract Compositions of actinolite, hornblende and cummingtonite, together with pyroxene and plagioclase, are studied in basic intrusions in the Dalradian of north-east Scotland, and the Glen Scaddle complex in the West Moine. Amphibolitization is due to influx of water from the country rocks. Pyroxene compositions are found to have adjusted to the regional metamorphic environment. Owing to the difficulty of diffusion of Al and Si, calcic amphiboles are zoned and commonly contain quartz blebs. Discontinuities in zoning give rise to actinolite-hornblende pairs. Compared with north-east Scotland, disequilibrium is less strong in the Glen Scaddle area: in the latter, plagioclase compositions have been greatly changed, Na partition between hornblende and plagioclase is close to equilibrium, the maximum Al content of hornblende is lower and zoning patterns are more consistent. The Fe/Mg ratio in calcic amphiboles varies with Al content, while approaching equilibrium partition with other minerals. Both zoning patterns and Fe/Mg partition with cummingtonite suggest that Fe/Mg of the calcic amphiboles increases more strongly with increasing (Alvi+Fe3+) than can be explained simply by substitution of Al,Fe3+ for Mg on M2. Model reactions for amphibole formation are constructed. Cummingtonite formed at lower chemical potential of CaO than actinolite: Ca was exchanged for Mg,Fe between orthopyroxene-derived and clinopyroxene-derived local systems. Both cummingtonite and actinolite were formed because of kinetic constraints, as intermediate reaction products: actinolite-hornblende pairs represent disequilibrium. This work suggests that many occurrences of actinolite with hornblende, where the minerals are zoned, may also be due to diffusion kinetics.  相似文献   

19.
The 2 km wide contact aureole produced from serpentinite bythe intrusion of the Mount Stuart Batholith into the IngallsComplex at Paddy-Go-Easy Pass contains the following ultramaficassemblages, in order of increasing grade: serpentine-forsterite-diopside,serpentine-forsterite-tremolite, forsterite-talc, forsterite-anthophyllite,forsterite-enstatite-anthophyllite, forsterite-enstatite-chlorite,forsterite-enstatite-spinel. Associated metarodingites displayfive metamorphic zones, the diagnostic assemblages of whichare, in increasing grade: grossular-idocrase-chlorite, grossular-diopside-chlorite,epidote-diopside-chlorite, epidote-diopside-spinel, plagioclase-grossular-diopside.Mafic hornfels in the aureole contains no orthopyroxene, indicatingthat the conditions of pyroxene hornfels facies were not reached. The breakdown of chlorite is best displayed in aluminous blackwallreaction zones around mafic inclusions in the peridotite. Attemperatures above those of the anthophyllite-out isograd, butwithin the field of forsterite+tremolite, these chlorite-richrocks react to form the assemblage: forsterite-enstatite-spinel.Calculations show that cordierite did not form as a result ofchlorite breakdown in the natural system because impurities,such as iron and chromium, displaced the equilibrium: forsterite+cordierite=enstatite+spinelto much lower pressures than the three kilobars found in thepure system. The primary chromite of the peridotite has been altered to chrome-magnetitein the serpentinite. This alteration seems to be isochemicalover the whole rock, as true chromite, formed by metamorphism,occurs at grades above that of the forsterite-enstatite-anthophylliteassemblage. Calcic amphibole in high-grade metaperidotite is tremolite,even in the presence of aluminous chromite, whereas that inmetamorphosed blackwall rock grades from tremolite into hornblende.The pattern of substitution appears to be: Mg2Si3(Na,K)(AlVI)2(AlIV)3.  相似文献   

20.
IIb trioctahedral chlorite in the Barberton greenstone belt (BGB) metavolcanic rocks was formed during pervasive greenschist metamorphism. The chem‐ical composition of the chlorite is highly variable, with the Fe/(Fe+Mg) ratio ranging from 0.12 to 0.8 among 53 samples. The chemical variation of the chlorite results from the chemical diversity of the host rock, especially the MgO content of the rock, but major details of the variation pattern of the chlorite are due to the crystal structure of the chlorite. All major cation abundances in the chlorite are strongly correlated with each other. Sil‐icon increases with Mg and decreases with Fe, while AlIV and AlVI decrease with Mg and increase with Fe2+. A complex exchange vector explains over 90% of the chlorite compositional variation: Mg4SiFe2+ −3AlVI −1 AlIV −1, which has 3 parts Fe-Mg substitution coupled with one part tschermakite substitution. This ratio is required to maintain the charge and site balances and the dimensional fit between the tetrahedral and octahedral sheets. The subtle change in Al substitution in chlorite implies that AlVI is preferentially ordered in the M(4) site, and about 84% of the AlVI present is in the M(4) sites when they are nearly filled with AlVI. Based on 47 analyzed chlorite-bearing rock samples, chlorite (Chl) composition is strongly correlated with the MgO content of the host rock. Calculated correlation coefficients are +0.91 for SiO2Chl-MgORock, −0.87 for Al2O3Chl-MgORock, +0.89 for MgOChl-MgORock, and −0.85 for FeOChl-MgORock. Only weak correlations have been found between chlorite oxides and other oxides of rock (between same oxides in chlorite and rock: SiO2−0.67, Al2O3 + 0.59, FeO −0.41). However, MgOChl is saturated at about 36 wt% in rocks that have MgO above 22 wt%.The MgOChl is about 5 wt% when the host rock approaches 0 wt% of MgO. This implies that Mg substituting into the chlorite is approximately limited to 1.5–9.2 Mg atoms per formula unit and 1.0–3.2 AlIV. Chlorite geothermometers can not be applied to all BGB samples. However, the empirical chlorite geothermometer based on AlIV of chlorite may be applicable to chlorites formed under metamorphic conditions because it can predict the chemical composition of the chlorite from basaltic and dacitic samples in this study. An estimated temperature of about 320°C for the greenschist metamorphism of the greenstone belt through this geothermometer is consistent with that obtained by other geothermometers. Received: 22 January 1996 / Accepted: 15 August 1996  相似文献   

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