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1.
Garnet-clinopyroxene geothermometry has been applied to numerous rock types from the blueschist and eclogite terrain of the Sesia zone in the Western Alps. Discrepancies in apparent temperatures of up to 600° C have been found suggesting substantial deviation from ideal behaviour of the garnet-clinopyroxene equilibria in certain assemblages. Assemblages containing jadeitic pyroxenes rather than omphacitic or diopsidic pyroxenes yield very low K D (2.0) values and correspondingly high apparent temperatures (> 1,000° C). The garnets coexisting with high-Na pyroxenes have compositions similar to those coexisting with omphacitic pyroxenes. Departure from ideal behaviour of these garnets is likely to be minor and is accomodated in the formulation of the geothermometer. Numerous examples of coexisting garnet-clinopyroxene pairs indicate that there is no obvious relationship of K D with jadeite content in pyroxenes with jadeite content less than 70%, but at higher values, K D varies inversely with the jadeite content. The dependence of K D upon the jadeite content in the high-Na pyroxenes is believed to be due to the preference of M2 sites for Fe2+ in the enstatite-jadeite substitution (Fe2+MgNa–1Al–1). This substitution is usually very limited and has no demonstrable effect upon X Fe Cpx when the M1 (Fe2++Mg) content of the pyroxenes is high as in omphacitic and diopsidic pyroxenes. However, when the M1 (Fe2++Mg) content is low, as in jadeitic pyroxenes, the non-ideality of the enstatite type exchange has a marked effect on X Fe Cpx and consequently on garnet-clinopyroxene calculations.  相似文献   

2.
The compositions of metamorphic pyroxenes from blueschists in northern New Caledonia are investigated. Aegerine-augite occurs in siliceous metasediments and aegerine in some low-grade sodic basic schists. Calcic metamorphic pyroxene (omphacite and chloromelanite) appears first in metabasalts in higher grades of the lawsonite zone and is widespread in metamorphosed igneous rocks and quartzofeldspathic gneisses of the epidote zone. Omphacites in basic rocks have higher Mg∶Fe ratios and are less jadeitic than omphacites from adjacent interbedded quartzofeldspathic gneisses. With increasing metamorphic grade pyroxenes become more jadeitic and diopsidic at the expense of their acmite component. Elemental partitioning between coexisting pyroxenes, garnets and amphiboles from in situ regional metamorphic rocks is generally regular, suggesting equilibrium crystallization. Omphacite appears to be a stable phase within blueschist facies over a temperature range of at least 350° to 550° C. The “eclogitic” assemblage almandine-omphacite is stable within the earth's crust in metamorphosed sediments and igneous rocks over a temperature range of 400° to at least 550° C. No estimate of absolute pressures involved in metamorphism in the Ouégoa district can yet be made.  相似文献   

3.
Abstract Eclogites are distributed for more than 500 km along a major tectonic boundary between the Sino-Korean and Yangtze cratons in central and eastern China. These eclogites usually have high-P assemblages including omphacite + kyanite and/or coesite (or its pseudomorph), and form a high-P eclogite terrane. They occur as isolated lenses or blocks 10 cm to 300 m long in gneisses (Type I), serpentinized garnet peridotites (Type II) and marbles (Type III). Type I eclogites were formed by prograde metamorphism, and their primary metamorphic mineral assemblage consists mainly of garnet [pyrope (Prp) = 15–40 mol%], omphacite [jadeite (Jd) = 34–64 mol%], pargasitic amphibole, kyanite, phengitic muscovite, zoisite, an SiO2 phase, apatite, rutile and zircon. Type II eclogites characteristically contain no SiO2 phase, and are divided into prograde eclogites and mantle-derived eclogites. The prograde eclogites of Type II are petrographically similar to Type I eclogites. The mantle-derived eclogites have high MgO/(FeO + Fe2O3) and Cr2O3 compositions in bulk rock and minerals, and consist mainly of pyrope-rich garnet (Prp = 48–60 mol%), sodic augite (Jd = 10–27 mol%) and rutile. Type III eclogites have an unusual mineral assemblage of grossular-rich (Grs = 57 mol%) garnet + omphacite (Jd = 30–34 mol%) + pargasite + rutile. Pargasitic and taramitic amphiboles, calcic plagioclase (An68), epidote, zoisite, K-feldspar and paragonite occur as inclusions in garnet and omphacite in the prograde eclogites. This suggests that the prograde eclogites were formed by recrystallization of epidote amphibolite and/or amphibolite facies rocks with near-isothermal compression reflecting crustal thickening during continent–continent collision of late Proterozoic age. Equilibrium conditions of the prograde eclogites range from P > 26 kbar and T= 500–750°C in the western part to P > 28 kbar and T= 810–880°C in the eastern part of the high-P eclogite terrane. The prograde eclogites in the eastern part are considered to have been derived from a deeper position than those in the western part. Subsequent reactions, manifested by (1) narrow rims of sodic plagioclase or paragonite on kyanite and (2) symplectites between omphacite and quartz are interpreted as an effect of near-isothermal decompression during the retrograde stage. The conditions at which symplectites re-equilibrated tend to increase from west (P < 10 kbar and T < 580°C) to east (P > 9 kbar and T > 680°C). Equilibrium temperatures of Type II mantle-derived eclogites and Type III eclogite are 730–750°C and 680°C, respectively.  相似文献   

4.
The transition between blueschist and eclogite plays an important role in subduction zones via dehydration and densification processes in descending oceanic slabs. There are a number of previous petrological studies describing potential mineral reactions taking place at the transition. An experimental determination of such reactions could help constrain the pressure–temperature conditions of the transition as well as the processes of dehydration. However, previous experimental contributions have focused on the stability of spontaneously formed hydrous minerals in basaltic compositions rather than on reactions among already formed blueschist facies minerals. Therefore, this study conducted three groups of experiments to explore the metamorphic reactions among blueschist facies minerals at conditions corresponding to warm subduction, where faster reaction rates are possible on the time scale of laboratory experiments. The first group of experiments was to establish experimental reversals of the reaction glaucophane+paragonite to jadeite+pyrope+quartz+H2O over the range of 2.2–3.5 GPa and 650–820°C. This reaction has long been treated as key to the blueschist–eclogite transition. However, only the growth of glaucophane+paragonite was observed at the intersectional stability field of both paragonite and jadeite+quartz, confirming thermodynamic calculations that the reaction is not stable in the system Na2O–MgO–Al2O3–SiO2–H2O. The second set of experiments involved unreversed experiments using glaucophane+zoisite ±quartz in low‐Fe and Ca‐rich systems and were run at 1.8–2.4 GPa and 600–780°C. These produced omphacite+paragonite/kyanite+H2O accompanied by compositional shifts in the sodium amphibole, glaucophane, towards sodium–calcium amphiboles such as winchite (?(CaNa)(Mg4Al)Si8O22(OH)2) and barroisite (?(CaNa)(Mg3Al2)(AlSi7)O22(OH)2). This suggests that a two‐step dehydration occurs, first involving the breakdown of glaucophane+zoisite towards a paragonite‐bearing assemblage, then the breakdown of paragonite to release H2O. It also indicates that sodium–calcium amphibole can coexist with eclogite phases, thereby extending the thermal stability of amphibole to greater subduction zone depths. The third set of experiments was an experimental investigation at 2.0–2.4 GPa and 630–850°C involving a high‐Fe (Fe#=Fetotal/(Fetotal+Mg)≈0.36) natural glaucophane, synthetic paragonite and their eclogite‐forming reaction products. The results indicated that garnet and omphacite grew over most of these pressure–temperature conditions, which demonstrates the importance of Fe‐rich glaucophane in forming the key eclogite assemblage of garnet+omphacite, even under warm subduction zone conditions. Based on the experiments of this study, reaction between glaucophane+zoisite is instrumental in controlling dehydration processes at the blueschist–eclogite transition during warm subduction.  相似文献   

5.
Abstract Textural evolution and compositional variation of clinopyroxenes in Ward Creek metabasites are described. Pyroxenes change, with increasing grade, from finegrained aggregates through fan-shaped medium-grained prisms to blocky coarse crystals. Characteristic features of metamorphic pyroxenes include: (1) the occurrence of coexisting pyroxene pairs, the compositions of which are used to delineate compositional gaps; (2) the existence of large compositional variations of pyroxenes, within a single specimen, which record a considerable span of P and/or T for crystallization; and, (3) the development of compositional trends in single specimens and in three metamorphic zones which are progressive in nature. The first formed clinopyroxene (Jd20Aug65Ac15) in the lower lawsonite zone mimics the composition of relict igneous augite. It changes continuously, with increasing grade, at nearly constant low XJd content towards acmite. At a composition around Jd20Aug30Ac50, the trend turns towards jadeite and intersects a solvus to form two coexisting clinopyroxenes in the middle lawsonite zone. At higher grade, the compositional gap becomes restricted towards the jadeite-omphacite join and clinopyroxene increases in XJd toward jadeite. A reversed compositional trend occurs at higher grade; clinopyroxenes decrease in jadeite component at nearly constant Aug/Ac ratio of 50/50 and finally become omphacite in the uppermost pumpellyite and epidote zones. The Na–Ca pyroxenes, close to the binary join Jd–Ac, occur in the lawsonite- and pumpellyite-zones, ranging from XJd= 1.0–0.30 together with Ab and Qz. The ubiquitous occurrence of aragonite at temperature estimates of 170–240° C by Taylor & Coleman (1968) for these zones does not support the low-temperature extrapolation of the Jd–Ab–Qz curve by Holland (1980). The estimated metamorphic field gradient indicates an inflection point at 7 kbar, 200° C. Below this, blueschist facies metamorphism proceeded under dominant pressure-increase from 4 to 7 kbar at nearly constant temperature, about 150–200° C, whereas at higher grade recrystallization, above the inflection point, the metamorphic temperature increased from 200 to 350° C at nearly constant pressure, about 7–8 kbar. Such an inflection point suggests the depth of underplating of either seamounts or accretionary packages in a subduction zone.  相似文献   

6.
Coexisting garnet blueschist and eclogite from the Chinese South Tianshan high‐pressure (HP)–ultrahigh‐pressure (UHP) belt consist of similar mineral assemblages involving garnet, omphacite, glaucophane, epidote, phengite, rutile/sphene, quartz and hornblendic amphibole with or without paragonite. Eclogite assemblages generally contain omphacite >50 vol.% and a small amount of glaucophane (<5 vol.%), whereas blueschist assemblages have glaucophane over 30 vol.% with a small amount of omphacite which is even absent in the matrix. The coexisting blueschist and eclogite show dramatic differences in the bulk‐rock compositions with higher X(CaO) [=CaO/(CaO + MgO + FeOtotal + MnO + Na2O)] (0.33–0.48) and lower A/CNK [=Al2O3/(CaO + Na2O + K2O)] (0.35–0.56) in eclogite, but with lower X(CaO) (0.09–0.30) and higher A/CNK (0.65–1.28) in garnet blueschist. Garnet in both types of rocks has similar compositions and exhibits core–rim zoning with increasing grossular and pyrope contents. Petrographic observations and phase equilibria modelling with pseudosections calculated using thermocalc in the NCKMnFMASHO system for the coexisting garnet blueschist and eclogite samples suggest that the two rock types share similar P–T evolutional histories involving a decompression with heating from the Pmax to the Tmax stage and a post‐Tmax decompression with slightly cooling stage, and similar P–T conditions at the Tmax stage. The post‐Tmax decompression is responsible for lawsonite decomposition, which results in epidote growth, glaucophane increase and omphacite decrease in the blueschist, or in an overprinting of the eclogitic assemblage by a blueschist assemblage. Calculated P–X(CaO), P–A/CNK and P–X(CO2) pseudosections indicate that blueschist assemblages are favoured in rocks with lower X(CaO) (<0.28) and higher A/CNK (>0.75) or fluid composition with higher X(CO2) (>0.15), but eclogite assemblages preferentially occur in rocks with higher X(CaO) and lower A/CNK or fluid composition with lower X(CO2). Moreover, phase modelling suggests that the coexistence of blueschist and eclogite depends substantially on P–T conditions, which would commonly occur in medium temperatures of 500–590 °C under pressures of ~17–22 kbar. The modelling results are in good accordance with the measured bulk‐rock compositions and modelled temperature results of the coexisting garnet blueschist and eclogite from the South Tianshan HP–UHP belt.  相似文献   

7.
The phase relations of pyroxenes, amphiboles and associated minerals in metamorphic rocks of the Franciscan Complex can be graphically depicted on a ternary diagram which has at its apices the metamorphic clinopyroxene end members, viz NaAl-NaFe3+-Ca(Fe2+, Mg). Phases are plotted by projection from a constant subassemblage of minerals. This analysis allows interpretation of the effects of pressure, temperature, bulk rock composition and fluid composition on stability of minerals within the Franciscan.Pyroxenes in meta-igneous rocks and metagraywackes have a limited compositional range and fall into two groups: the omphacites, with 50±5% diopside +hedenbergite component; and the jadeitic pyroxenes with 10±5% diopside+hedenbergite. Pyroxenes intermediate between these two groups are unstable relative to assemblages containing Na-amphibole+other minerals.Coexisting pyroxenes and amphiboles in eclogites and associated coarse blueschists comprise equilibrium assemblages, and the proportion of pyroxene to amphibole is a function of rock composition. Eclogites are stable at higher temperature than regionally developed fine-grained greenstones and blueschists in the Franciscan, and at higher pressure than amphibolites. X H2O fluid is not an important factor in the stability of Franciscan eclogite relative to amphibolite.  相似文献   

8.
Calculated phase equilibria among the minerals sodic amphibole, calcic amphibole, garnet, chloritoid, talc, chlorite, paragonite, margarite, omphacite, plagioclase, carpholite, zoisite/clinozoisite, lawsonite, pyrophyllite, kyanite, sillimanite, quartz and H2O are presented for the model system Na2O-CaO-FeO-MgO-Al2O3-SiO2-H2O (NCFMASH), which is relevant for many greenschist, blueschist, amphibolite and eclogite facies rocks. Using the activity-composition relationships for multicomponent amphiboles constrained by Will and Powell (1992), equilibria containing coexisting calcic and sodic amphiboles could be determined. The blueschist–greenschist transition reaction in the NCFMASH system, for example, is defined by the univariant reaction sodic amphibole + zoisite = calcic amphibole + chlorite + paragonite + plagioclase (+ quartz + H2O) occurring between approximately 420 and 450 °C at 9.5 to 10 kbar. The calculated petrogenetic grid is a valuable tool for reconstructing the PT-evolution of metabasic rocks. This is shown for rocks from the island of Samos, Greece. On the basis of mineral and whole rock analyses, PT-pseudosections were calculated and, together with the observed mineral assemblages and reaction textures, are used to reconstruct PT-paths. For rocks from northern Samos, pseudomorphs after lawsonite preserved in garnet, the assemblage sodic amphibole-garnet-paragonite-chlorite-zoisite-quartz and the retrograde appearance of albitic plagioclase and the formation of calcic amphibole around sodic amphibole constrain a clockwise PT-path that reaches its thermal maximum at some 520 °C and 19 kbar. The derived PT-trajectory indicates cooling during exhumation of the rocks and is similar to paths for rocks from the western part of the Attic-Cycladic crystalline complex. Rocks from eastern Samos indicate lower pressures and are probably related to high-pressure rocks from the Menderes Massif in western Turkey. Received: 8 July 1997 / Accepted: 11 February 1998  相似文献   

9.
Kyanite‐ and phengite‐bearing eclogites have better potential to constrain the peak metamorphic P–T conditions from phase equilibria between garnet + omphacite + kyanite + phengite + quartz/coesite than common, mostly bimineralic (garnet + omphacite) eclogites, as exemplified by this study. Textural relationships, conventional geothermobarometry and thermodynamic modelling have been used to constrain the metamorphic evolution of the Tromsdalstind eclogite from the Tromsø Nappe, one of the biggest exposures of eclogite in the Scandinavian Caledonides. The phase relationships demonstrate that the rock progressively dehydrated, resulting in breakdown of amphibole and zoisite at increasing pressure. The peak‐pressure mineral assemblage was garnet + omphacite + kyanite + phengite + coesite, inferred from polycrystalline quartz included in radially fractured omphacite. This omphacite, with up to 37 mol.% of jadeite and 3% of the Ca‐Eskola component, contains oriented rods of silica composition. Garnet shows higher grossular (XGrs = 0.25–0.29), but lower pyrope‐content (XPrp = 0. 37–0.39) in the core than the rim, while phengite contains up to 3.5 Si pfu. The compositional isopleths for garnet core, phengite and omphacite constrain the P–T conditions to 3.2–3.5 GPa and 720–800 °C, in good agreement with the results obtained from conventional geothermobarometry (3.2–3.5 GPa & 730–780 °C). Peak‐pressure assemblage is variably overprinted by symplectites of diopside + plagioclase after omphacite, biotite and plagioclase after phengite, and sapphirine + spinel + corundum + plagioclase after kyanite. Exhumation from ultrahigh‐pressure (UHP) conditions to 1.3–1.5 GPa at 740–770 °C is constrained by the garnet rim (XCaGrt = 0.18–0.21) and symplectite clinopyroxene (XNaCpx = 0.13–0.21), and to 0.5–0.7 GPa at 700–800 °C by sapphirine (XMg = 0.86–0.87) and spinel (XMg = 0.60–0.62) compositional isopleths. UHP metamorphism in the Tromsø Nappe is more widespread than previously known. Available data suggest that UHP eclogites were uplifted to lower crustal levels rapidly, within a short time interval (452–449 Ma) prior to the Scandian collision between Laurentia and Baltica. The Tromsø Nappe as the highest tectonic unit of the North Norwegian Caledonides is considered to be of Laurentian origin and UHP metamorphism could have resulted from subduction along the Laurentian continental margin. An alternative is that the Tromsø Nappe belonged to a continental margin of Baltica, which had already been subducted before the terminal Scandian collision, and was emplaced as an out‐of‐sequence thrust during the Scandian lateral transport of nappes.  相似文献   

10.
The phase relations of divariant and trivariant assemblages involving combinations of phengite, chlorite, biotite, K-feldspar, quartz and H2O in the KFASH, KMASH and KFMASH systems were calculated using a single thermodynamic data set (Holland and Powell 1998). The stability fields of the various equilibria are represented in P-T projections by contouring sets of compositional isopleths for the Tschermak (Al2(Fe,Mg)−1Si−1) and FeMg−1 exchanges controlled by the coexisting phases. Five multivariant continuous equilibria, which occur in different regions of P-T-X space, are calibrated as thermobarometers in metamorphic rocks of pelitic to quartzofeldspathic composition. More subtle P-T information, relating to the trajectories (dT/dz) along which reacting rocks have been buried or exhumed, can be extracted from the continuous reactions by investigating the recorded compositional trends in the Al2(Fe,Mg)−1Si−1 and FeMg−1 solutions. Singularities in P-T space are associated with some of these reactions and may result in unusual mineral textures and compositional trends. A fluid-absent singularity has particular petrological significance because it marks the transition between hydration and dehydration along a single reaction with increasing pressure and temperature. This behaviour causes the sequence of reactions among these minerals observed during metamorphism to be critically dependent on the P-T trajectory. Thermobarometric calculations show good agreement with respect to experimental and field-based data for phengite compositions less than about 50 mol% celadonite (<∼3.5 Si p.f.u. phengite). Received: 15 November 1999 / Accepted: 3 April 2000  相似文献   

11.
Abstract Sodic amphiboles are common in Franciscan type II and type III metabasites from Cazadero, California. They occur as (1) vein-fillings, (2) overgrowths on relict augites, (3) discrete tiny crystals in the groundmass, and (4) composite crystals with metamorphic Ca–Na pyroxenes in low-grade rocks. They become coarse-grained and show strong preferred orientation in schistose high-grade rocks. In the lowest grade, only riebeckite to crossite appears; with increasing grade, sodic amphibole becomes, first, enriched in glaucophane component, later coexists with actinolite, and finally, at even higher grade, becomes winchite. Actinolite first appears in foliated blueschists of the upper pumpellyite zone. It occurs (1) interlayered on a millimetre scale with glaucophane prisms and (2) as segments of composite amphibole crystals. Actinolite is considered to be in equilibrium with other high-pressure phases on the basis of its restricted occurrence in higher grade rocks, textural and compositional characteristics, and Fe/Mg distribution coefficient between actinolite and chlorite. Detailed analyses delineate a compositional gap for coexisting sodic and calcic amphiboles. At the highest grade, winchite appears at the expense of the actinolite–glaucophane pair. Compositional characteristics of Franciscan amphiboles from Ward Creek are compared with those of other high P/T facies series. The amphibole trend in terms of major components is very sensitive to the metamorphic field gradient. Na-amphibole appears at lower grade than actinolite along the higher P/T facies series (e.g. Franciscan and New Caledonia), whereas reverse relations occur in the lower P/T facies series (e.g. Sanbagawa and New Zealand). Available data also indicate that at low-temperature conditions, such as those of the blueschist and pumpellyite–actinolite facies, large compositional gaps exist between Ca- and Na-amphiboles, and between actinolite and hornblende, whereas at higher temperatures such as in the epidote–amphibolite, greenschist and eclogite facies, the gaps become very restricted. Common occurrence of both sodic and calcic amphiboles and Ca–Na pyroxene together with albite + quartz in the Ward Creek metabasites and their compositional trends are characteristic of the jadeite–glaucophane type facies series. In New Caledonia blueschists, Ca–Na pyroxenes are also common; Na-amphiboles do not appear alone at low grade in metabasites, instead, Na-amphiboles coexist with Ca-amphiboles throughout the progressive sequence. However, for metabasites of the intermediate pressure facies series, such as those of the Sanbagawa belt, Japan and South Island, New Zealand, Ca–Na pyroxene and glaucophane are not common; sodic amphiboles are restricted to crossite and riebeckite in composition and clinopyroxenes to acmite and sodic augite, and occur only in Fe2O3-rich metabasites. The glaucophane component of Na-amphibole systematically decreases from Ward Creek, New Caledonia, through Sanbagawa to New Zealand. This relation is consistent with estimated pressure decrease employing the geobarometer of Maruyama et al. (1986). Similarly, the decrease in tschermakite content and increase in NaM4 of Ca-amphiboles from New Zealand, through Sanbagawa to New Caledonia is consistent with the geobarometry of Brown (1977b). Therefore, the difference in compositional trends of amphiboles can be used as a guide for P–T detail within the metamorphic facies series.  相似文献   

12.
Spinel is widespread in the ultramafic core rocks of zoned late Precambrian mafic–ultramafic complexes from the Eastern Desert of Egypt. These complexes; Gabbro Akarem, Genina Gharbia and Abu Hamamid are Precambrian analogues of Alaskan-type complexes, they are not metamorphosed although weakly altered. Each intrusion is composed of a predotite core enveloped by pyroxenites and gabbros at the margin. Silicate mineralogy and chemistry suggest formation by crystal fractionation from a hydrous magma. Relatively high Cr2O3 contents are recorded in pyroxenes (up to 1.1 wt.%) and amphiboles (up to 1.4 wt.%) from the three plutons. The chrome spinel crystallized at different stages of melt evolution; as early cumulus inclusions in olivine, inclusions in pyroxenes and amphiboles and late-magmatic intercumulus phase. The intercumulus chrome spinel is homogenous with narrow-range of chemical composition, mainly Fe3+-rich spinel. Spinel inclusions in clinopyroxene and amphibole reveal a wide range of Al (27–44 wt.% Al2O3) and Mg (6–13 wt.% MgO) contents and are commonly zoned. The different chemistries of those spinels reflect various stages of melt evolution and re-equilibration with the host minerals. The early cumulus chrome spinel reveals a complex unmixing structures and compositions. Three types of unmixed spinels are recognized; crystallographically oriented, irregular and complete separation. Unmixing products are Al-rich (Type I) and Fe3+-rich (Type II) spinels with an extensive solid solution between the two end members. The compositions of the unmixed spinels define a miscibility gap with respect to Cr–Al–Fe3+, extending from the Fe3+–Al join towards the Cr corner. Spinel unmixing occurs in response to cooling and the increase in oxidation state. The chemistry and grain size of the initial spinel and the cooling rate control the type of unmixing and the chemistry of the final products. Causes of spinel unmixing during late-magmatic stage are analogous to those in metamorphosed complexes. The chemistry of the unmixed spinels is completely different from the initial spinel composition and is not useful in petrogenetic interpretations. Spinels from oxidized magmas are likely to re-equilibrate during cooling and are not good tools for genetic considerations.  相似文献   

13.
The Cazadero blueschist allochthon lies within the Central MelangeBelt of the Franciscan assemblage in the northern Coast Rangeof California. Mineral compositions and assemblages of morethan 200 blueschists from Ward Creek were investigated. Theresults delineate lawsonite-, pumpellyite-, and epidote-zones.The lawsonite and pumpellyite zones are equivalent to the TypeII metabasites of Coleman & Lee (1963) and are characterizedby well-preserved igneous textures, relict augite, and pillowstructures, whereas epidote zone rocks are equivalent to theType III strongly deformed and schistose metabasites. Chlorite,phengite, aragonite, sphene, and minor quartz and albite areubiquitous. The lawsonite zone metabasites contain lawsonite ( < 3 wt.per cent Fe2O3), riebeckite-crossite, chlorite, and Ca-Na-pyroxene;some rocks have two distinct clinopyroxenes separated by a compositionalgap. The clinopyroxene of the lowest grade metabasites containsvery low Xjd. In pumpellyite zone metabasites, the most commonassemblages contain Pm + Cpx + Gl + Chl and some samples withhigher Al2O3 and/or Fe2O3 have Pm + Lw + Cpx + Chl, Actinolitejoins the above assemblage in the upper pumpellyite zone wherethe actinolite-glaucophane compositional gap is well defined.The epidote zone metabasites are characterized by the assemblagesEp + Cpx + two amphiboles + Chl, Lw + Pm + Act + Chl, and Ep+ Pm + two amphiboles + Chl depending on the Fe2O3 content ofthe rock. In the upper epidote zone, winchite appears, Fe-freelawsonite is stable, pumpellyite disappears and omphacite containsvery low Ac component. Therefore, the common assemblages areEp + winchite + Lw, and Lw + Omp + winchite. With further increasein metamorphic grade, epidote becomes Al-rich and lawsoniteis no longer stable. Hence Ep + winchite + omphacite ? garnetis characteristic. Mineral assemblages and paragenetic sequences delineate threediscontinuous reactions: (1) pumpellyite-in; (2) actinolite-in;and (3) epidote-in reactions. Using the temperatures estimatedby Taylor & Coleman (1968) and phase equilibria for Ca-Na-pyroxenes,the P–T positions of these reactions and the metamorphicgradient are located. All three metabasite zones occur withinthe aragonite stability field and are bounded by the maximumpressure curve of Ab = Jd + Qz and the maximum stabilities ofpumpellyite and lawsonite. The lawsonite zone appears to bestable at T below 200?C with a pressure range of 4–6?5kb; the pumpellyite zone between 200 and 290?C and the epidotezone above 290?C with pressure variation between 6?5 and 9 kb.The metamorphic field gradient appears to have a convex naturetowards higher pressure. A speculative model of underplatingseamounts is used to explain such feature.  相似文献   

14.
Sodic pyroxene (jadeite content X jd=0.1–0.3) occurs locally as small inclusions within, albite porphyroblasts and in the matrix of hematite-bearing quartz schists in the Sanbagawa (Sambagawa) metamorphic belt, central Shikoku, Japan. The sodic, pyroxene-bearing samples are characteristically free from chlorite and their typical mineral assemblage is sodic pyroxene+subcalcic (or sodic) amphibole+phengitic mica+albite+quartz+hematite+titanite±epidote. Spessartine-rich garnet occurs in Mn-rich samples. Sodic pyroxene in epidote-bearing samples tends to be poorer in acmite content (average X Acm=0.26–0.50) than that in the epidote-free samples (X Acm=0.45–0.47). X Jd shows no systematic relationship to metamorphic grade, and is different among the three sampling regions [Saruta-gawa, Asemi-gawa and Bessi (Besshi)]. The average X Jd of the Saruta-gawa samples (0.21–0.29) is higher than that of the Asemi-gawa (0.13–0.17) and Bessi (0.14–0.23). The P-T conditions of the Asemi-gawa and Bessi regions are estimated at 5.5–6.5 kbar, >360°C in the chlorite zone, 7–8.5 kbar, 440±15°C in the garnet zone and 8–9.5 kbar, 520±25°C in the albite-biotite zone. Metamorphic pressure of the Saruta-gawa region is systematically 1–1.5 kbar higher than that of the Asemi-gawa and Bessi regions, and materials of the Saruta-gawa region have been subducted to a level 3–5 km deeper than materials that underwent metamorphism at equivalent temperatures and are now exposed in the Asemi-gawa and Bessi regions. Pressure slightly increases toward the north (structurally high levels) through the Sanbagawa belt of central shikoku. Two types of zonal structure were observed in relatively coarse-grained sodic pyroxenes in the matrix. One type is characterized by increasing X Jd from core to rim, the other type by decreasing X Jd from core to rim. Both types of zoned pyroxenes show an increase in X Fe 2+[=Fe2+/(Fe2++Mg)] from core to rim. The first type of zoning was observed in a sample from the chlorite zone of lowest grade, whereas the latter occurs in the garnet and albite-biotite zones of higher grade. The contrast in zonal structure implies that dP/dT during prograde metamorphism decreased with increasing metamorphic grade and may have been negative in some samples from the higher-grade zones. The estimated dP/dT of the prograde stage of the chlorite zone is 3.2 kbar/100°C, and that of the garnet and albite-biotite zones is -1.8 to 0.9 kbar/100°C. The variation of dP/dT at shallow and deep levels of a subduction system probably reflects the difference of heating duration and/or change in thermal gradient of the subduction zone by continuous cooling of the surrounding mantle.  相似文献   

15.
This paper reports the occurrence of vesvianite + wollastonite + grossular + diopside + microcline + quartz assemblage in an enclave of calc-silicate rocks occurring within quartzofeldspathic gneiss near Tatapani in the western part of Chhotanagpur Gneissic Complex. The enclave contains phlogopite-absent and phlogopite-bearing calc-silicate rocks, the latter being much more abundant than the former. The above assemblage occurs in the phlogopite-absent rock. Phlogopite-bearing rock contains the assemblage phlogopite + salite + microcline + plagioclase + quartz. A strong schistosity is developed in both the calc-silicate rocks and the minerals are syntectonic with the major foliation-forming event in the area. The vesuvianite-bearing assemblage is formed by amphibolite facies regional metamorphism of a calcareous protolith at pressure < 4 kbar and XCO 2 (fluid) < 0.15.  相似文献   

16.
The greenschist to amphibolite transition as modeled by the reaction zoisite+tremolite + quartz= anorthite+diopside+water has been experimentally investigated in the chemical system H2O−CaO− MgO−Al2O3−SiO2 over the range of 0.4–0.8 GPa. This reaction is observed to lie within the stability fields of anorthite + water and of zoisite + quartz, in accord with phase equilibrium principles, and its position is in excellent agreement with the boundary calculated from current internally-consistent data bases. The small dP/dT slope of 0.00216 GPa/K (21.6 bars/K) observed for this reaction supports the pressure-dependency of this transition in this chemical system. Experimental reversals of the Al content in tremolitic amphibole coexisting with zoisite, diopside, quartz, and water were obtained at 600, 650, and 700°C and indicated Al total cations (atoms per formula unit, apfu) of only up to 0.5±0.08 at the highest temperature. Thermodynamic analysis of these and previous compositional reversal data for tremolitic amphibole indicated that, of the activity/composition relationships considered, a two-site-coupled cation substitution model yielded the best fit to the data and a S 0 (1 bar, 298 K) of 575.4±1.6 J/K · mol for magnesio-hornblende. The calculated isopleths of constant Al content in the amphibole are relatively temperature sensitive with Al content increasing with increasing temperature and pressure. Finally, several experiments in the range of 1.0–1.3 GPa were conducted to define the onset of melting, and thus the upper-thermal limit, for this mineral assemblage, which must involve an invariant point located at approximately 1.05 GPa and 770°C. Received: 24 January 1997 / Accepted: 2 October 1997  相似文献   

17.
The high-pressure (HP) eclogite in the western Dabie Mountain encloses numerous hornblendes, mostly barroisite. Opinions on the peak metamorphic P-T condition, PT path and mineral paragenesis of it are still in dispute. Generally, HP eclogite involves garnet, omphacite, hornblendes and quartz, with or without glaucophane, zoisite and phengite. The garnet has compositional zoning with XMg increase, XCa and XMn decrease from core to rim, which indicates a progressive metamorphism. The phase equilibria of the HP eclogite modeled by the P-T pseudosection method developed recently showed the following: (1) the growth zonation of garnet records a progressive metamorphic PT path from pre-peak condition of 1.9–2.1 GPa at 508°C–514°C to a peak one of 2.3–2.5 GPa at 528°C–531°C for the HP eclogite; (2) the peak mineral assemblage is garnet+omphacite+glaucophane+quartz±phengite, likely paragenetic with lawsonite; (3) the extensive hornblendes derive mainly from glaucophane, partial omphacite and even a little garnet due to the decompression with some heating during the post-peak stage, mostly representing the conditions of about 1.4–1.6 GPa and 580°C–640°C, and their growth is favored by the dehydration of lawsonite into zoisite or epidote, but most of the garnet, omphacite or phengite in the HP eclogite still preserve their compositions at peak condition, and they are not obviously equilibrious with the hornblendes.  相似文献   

18.
The impure marbles of the internal Sesia-Lanzo Zone underwent a multi-stage metamorphic evolution of Alpine age and retain early-Alpine eclogitic assemblages, partially recrystallized under blueschist to greenschist facies conditions. These high-P assemblages consist of carbonates, phengite, quartz, omphacite, grossular-rich (locally spessartinic) garnet, zoisite and Al-rich titanite. Retrogressive stages are characterized by the growth of glaucophane, paragonite, phlogopite, tremolite and albite. Halogen-rich biotite and amphibole are also present. P-T estimates of the early-Alpine metamophism have been calculated from these unique high-P assemblages, in order to test the applicability of some calibrations to impure carbonate systems. In particular, some Gt-Cpx calibrations and the phengite geobarometer give results (T= 575 ± 45° C at 15 kbar for the eclogitic climax and T≤ 500° C at PH2O ≤ 9 kbar for early-Alpine retrogressive stages) which are within the range obtained from the surrounding lithologies. Phase relationships in P-T-XCO2 space indicate that mineral assemblages in the impure marbles coexisted with H2O-rich fluids (XCO2 <0.03) during their entire Alpine evolution.  相似文献   

19.
Coexisting zoisite and clinozoisite assemblages in biotite schists from the western Hohe Tauern, Austria, have been investigated with the electron microprobe, polarization optics, and X-ray diffractometer. Zoisite and clinozoisite show slight compositional zoning, ranging from the core to the rim from about 1.8 to 1.0 wt. % Fe in zoisite, and 4.0 to 3.0 wt. % Fe in clinozoisite. The results suggest a gap of composition between coexisting zoisite and clinozoisite under greenschist-amphibolite transition facies conditions.The optical orientation and 2V of zoisite vary considerably within single grains. Lamellar structures have been detected which may be produced by unmixing of zoisite. The Fe-poor lamellae have 2V z=20–50°, a dispersion r>v, and relatively low refringence, the Fe-rich lamellae have 2V z =90–100°, rv, and higher refringence. The optic axial planes of both lamellae systems deviate from the (100) cleavage by up to 15°, and suggest a deviation from orthorombic symmetry. The lattice constants of coexisting zoisite and clinozoisite are given.  相似文献   

20.
A computerised algorithm is used to arrange fluid-absent reactions about invariant points in P—T space for an end-member model of blueschist facies metamorphism at Port Macquarie, N.S.W., consisting of the nine phases quartz, albite, jadeite, lawsonite, zoisite, paragonite, glaucophane, pyrope and chlorite. Inspection of the print-out (a table of reaction take-off angles for each invariant point) indicates that this multisystem consists of two mutually exclusive sets of invariant points; lawsonite-absent, paragonite-absent and glaucophane-absent versus the other six. The algorithm is completely general for any two intensive variables and can treat solid solution minerals or degeneracy in reactions/invariant points.Terms ABS(X) Absolute value of X - A(J) Slope of reaction J in degrees - V(J) Denominator variable in the slope fraction for reaction J - R(K, J) Reaction coefficient of phase K in reaction J - S(K, J) Stability pointer for phase K in reaction J, in degrees - SGN (X) Library function: =–1 when X<0; =+1 when X0 - B(Q) Correct take-off angle for the Q-absent reaction in degrees  相似文献   

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