Metamorphic evolution of the Susunai metabasites in southern Sakhalin, Russian Republic

The Susunai Complex of southeast Sakhalin represents a subduction-related accretionary complex of pelitic and basic rocks. Two stages of metamorphism are recognized: (1) a local, low- P / T  event characterized by Si-poor calcic amphiboles; (2) a regional, high- P / T  event characterized by pumpellyite, actinolite, epidote, sodic amphibole, sodic pyroxene, stilpnomelane and aragonite. The major mineral assemblages of the high- P / T  Susunai metabasites contain pumpellyite+epidote+actinolite+chlorite, epidote+actinolite+chlorite, epidote+Na-amphibole+Na-pyroxene+chlorite+haematite. The Na- amphibole is commonly magnesioriebeckite. The Na-pyroxene is jadeite-poor aegirine to aegirine-augite. Application of empirically and experimentally based thermobarometers suggests peak conditions of T  =250–300 °C, P= 4.7–6 kbar. Textural relationships in Susunai metabasite samples and a petrogenetic grid calculated for the Fe³⁺-rich basaltic system suggest that pressure and temperature increased during prograde metamorphism.     

Phase petrology and P-T conditions of mafic blueschists from the Meliata unit, West Carpathians, Slovakia

Abstract Blueschists occurring as layers in calcite marbles of the Meliata unit occur along the so-called Roznava tectonic line situated in the southern part of the Gemericum, Slovakia. Mineral assemblages and compositions from seven blueschists localities and one occurrence of amphibolite facies rocks overprinted by blueschist metamorphism were investigated. The most common minerals in the blueschists are blue amphibole, epidote and albite. Some Fe²⁺- and Al-rich rocks also contain garnet and chloritoid, respectively. Na-pyroxene with a maximum 50% jadeite component was also found. The blue amphiboles correspond mostly to crossite and also to glaucophane and ferroglaucophane in some samples. Almandine- and spessartine-rich garnet has very low MgO content (<3 wt%). The Si content in phengite ranges between 3.3 and 3.5 pfu calculated on the basis of 11 oxygens. The zoning patterns of blue amphibole, garnet and chloritoid suggest their formation during a prograde stage of metamorphism. The P-T conditions of metamorphism are estimated to be about 380–460° C and 10–13 kbar. Pressures of 7.5–8.5 kbar and temperatures of 350–370° C were obtained for some actinolite- and aegirine-rich rocks. Apart from chlorite, other mafic minerals formed during retrograde metamorphism are biotite and occasionally also actinolite.     

Parageneses and compositions of amphiboles from Franciscan jadeite–glaucophane type facies series metabasites at Cazadero, California

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.     

Retrograde P-T-t path for the Voltri Massif eclogites (Ligurian Alps, Italy): some tectonic implications

The retrograde P-T trajectory of the eclogitic Fe-Ti-gabbros from the Ligurian Alps is constrained by the appearance of mineral parageneses post-dating the Na-clinopyroxene + garnet eclogitic assemblage and indicating the following sequence of metamorphic events: (1) amphibolitic stage— edenite/katophorite + plagioclase (An_33–43) + oxides in symplectitic aggregates; (2) glaucophanic stage— a porphyroblastic glaucophanic amphibole has overgrown the symplectite, winchite also occurs as thin rims around glaucophane and both amphiboles are, sometimes, armoured by atoll garnets; (3) albite-amphibolite stage—barroisite/katophorite + albite + epidote + oxides ± chlorite overprint the glaucophanic stage minerals; (4) greenschist stage—represented by actinolite + albite + epidote + oxide paragenesis.
The metamorphic evolution is complex and the decompression path, on a P–T diagram, is significantly different from those defined in the literature for the Voltri eclogites. The main features inferred from the P–T path are the following: (1) the pressure climax does not match the thermal climax, the maximum temperature conditions are in fact achieved during the early stage of uplift; (2) a decrease in temperature, suggested by the appearance of glaucophane after the amphibolitic symplectite; (3) successive uplift, probably accompanied by an increase in temperature. The complexity of the P-T path drawn for the Voltri eclogites can be explained with a mechanism of successive underthrusts propagating from the innermost to the outermost sector of the Ligurian Alps.     

Glaucophane-bearing assemblage overprinted by greenschist-facies metamorphism in the Variscan Kaczawa complex, Sudetes, Poland

An Early Palaeozoic (Ordovician ?) metamudstone sequence near Wojcieszow, Kaczawa Mts, Western Sudetes, Poland, contains numerous metabasite sills, up to 50 m thick. These subvolcanic rocks are of within-plate alkali basalt type. Primary igneous phases in the metabasites, clinopyroxene (salite) and kaersutite, are veined and partly replaced by complex metamorphic mineral assemblages. Particularly, the kaersutite is corroded and rimmed by zoned sodic, sodic–calcic and calcic amphiboles. The matrix is composed of actinolite, pycnochlorite, albite (An ≤ 0.5%), epidote (Ps 27–33), titanite, calcite, opaques and, occasionally, biotite, phengite and stilpnomelane. The sodic amphiboles are glaucophane to crossite in composition with Na^B from 1.9 to 1.6. They are rimmed successively by sodic–calcic and calcic amphiboles with compositions ranging from magnesioferri-winchite to actinolite. No compositions between Na^B= 0.92 and Na^B= 1.56 have been ascertained. The textures may be interpreted as representing a greenschist facies overprint on an earlier blueschist (or blueschist–greenschist transitional) assemblage. The presence of glaucophane and no traces of a jadeitic pyroxene + quartz association indicate pressures between 6 and 12 kbar during the high-pressure episode. Temperature is difficult to assess in this metamorphic event. The replacement of glaucophane by actinolite + chlorite + albite, with associated epidote, allows restriction of the upper pressure limit of the greenschist recrystallization to <8 kbar, between 350 and 450°C. The mineral assemblage representing the greenschist episode suggests the P–T conditions of the high-pressure part of the chlorite or lower biotite zone. The latest metamorphic recrystallization, under the greenschist facies, may have taken place in the Viséan.     

Mineralogy of New Caledonian metamorphic rocks

The chemistry and phase relations of calcic and sodic amphiboles in the Ouégoa blueschists are investigated. The first appearance of sodic amphiboles is controlled by bulkrock chemistry. Sodic amphibole appears first in weakly-metamorphosed pumpellyite metabasalts prior to the crystallization of lawsonite but does not crystallize in pelitic schists until the middle of the lawsonite zone; sodic amphibole continues as an apparently stable phase in rocks of all bulk compositions into, and throughout, the highest-grade rocks in the district. Calcic amphibole is widespread in metabasalts of the lawsonite and epidote zones and also occurs in metasediments of appropriate composition. Coexisting pairs of calcic and sodic amphiboles are common in metabasalts but they have also been found in some metasediments. A grunerite-riebeckite pair is described.Electron-probe analyses of 120 amphiboles from representative rock-types are presented in graphical form. Sodic amphiboles show an increased Mg/(Mg+Fe) ratio with increasing metamorphic grade. Sodic amphiboles in pelitic schists are ferroglaucophane in the lawsonite zone and crossite and glaucophane in the epidote zone. Sodic amphiboles in metabasalts are iron-rich crossites in weakly-metamorphosed rocks and more-magnesian crossites and glaucophanes in the lawsonite and epidote zones. The abrupt increase in Mg/(Mg+Fe) ratio in sodic amphiboles at the epidote isograd is attributed to the crystallization of epidote and almandine which take the place of lawsonite and spessartine of the lawsonite zone. Calcic amphiboles are fibrous actinolites in the lawsonite zone and grade with increasing Al and Na/Ca ratio into prismatic blue-green hornblendes (barroisites) in the upper epidote zone. In calcic amphiboles, increasing metamorphic grade effects the coupled substitution of (Na+Al) for (Ca+Mg) and a small increases in Fe/Mg ratio; octahedrally and tetrahedrally coordinated Al increases in an approximately 11 ratio. Both the calcic and the sodic amphiboles show an increase in A-site occupancy with increasing metamorphic grade. In two-amphibole assemblages Ti, Mn and K are concentrated in the calcic amphibole.The textural and chemical relations between coexisting calcic and sodic amphiboles are discussed. If the calcic and sodic amphiboles are an equilibrium pair then the data collected from the Ouégoa amphiboles gives a picture of a very asymmetric solvus in the system glaucophane-actinolite-hornblende, i.e. steep-sided to glaucophane and with a gentle slope to the calcic amphibole field; there is no indication of any termination of the solvus under the pressure-temperature conditions of crystallization of the Ouégoa schists.     

Metabasite amphiboles of the Scottish Dalradian

Blue-green hornblendes are observed in metabasite assemblages throughout the chlorite, biotite and garnet zones of the southwest Scottish Highlands. Actinolites are common in more Mg-rich metabasites in these zones. At low grade, hornblendes are relatively edenite-rich, and may sometimes occur together with a more Mg-rich, Al-poor actinolite. Within the garnet zone, hornblendes are pargasitic, showing extensive tschermakite substitution. Textural and chemical evidence do not indicate the presence of any miscibility gap between hornblende and actinolite within the chlorite to garnet zones in the southwest Highlands. The occurrence of hornblende-actinolite pairs in metabasites of the Scottish Dalradian, and perhaps also in other metamorphic terrains, is considered to reflect the incomplete chemical equilibration of lower grade actinolitic amphibole during prograde metamorphism, rather than a miscibility gap. The paucity of amphibole compositions intermediate between hornblende and actinolite in many metamorphic terrains is thought to reflect the rapid but continuous change of stable amphibole compositions in metabasites over a small range of increased metamorphic grade.     

The Serra da Graciosa A-type Granites and Syenites, southern Brazil. Part 3: Magmatic evolution and post-magmatic breakdown of amphiboles of the alkaline association

Amphiboles are the main mafic minerals in most metaluminous to peralkaline alkali-feldspar granites and syenites, and they usually preserve an important record of the compositional evolution of the melts from which they crystallize. In the alkaline association of the Serra da Graciosa A-type Granites and Syenites (southern Brazil), amphibole compositions span a large range, including calcic, sodic–calcic, and sodic amphiboles. Calcic amphiboles are typically observed in the metaluminous rocks, while sodic amphiboles are characteristic of the more strongly peralkaline rocks; sodic–calcic amphiboles are found in intermediate varieties. Compositional variations record the differentiation trends within two petrographic series of the alkaline association. The overall evolution of amphibole compositions is similar in both: they reveal a progressive increase in Na and Fe³⁺ with differentiation (increase in alkalinity of the magmas), a characteristic shared by undersaturated peralkaline (or agpaitic) differentiation trends. In detail, however, the evolutions of the amphibole compositions in the two series are distinct. In Alkaline series 1, the cores of the crystals form a continuum from calcic to sodic compositions, with the exception of a small compositional gap within the sodic–calcic amphiboles. The rims, however, show compositions that diverge from this main trend; this divergence results from increasing amounts of the oxy-amphibole component, and reflects more oxidizing conditions at the final stages of magmatic crystallization. In Alkaline series 2, these oxidation trends are much more subtle and a reverse trend is observed in the sodic amphiboles. Sodic–calcic amphiboles are in several cases replaced by intergrowths of post-magmatic sodic amphibole and Al-poor (“tetrasilicic”) biotite.     

Prograde metamorphic evolution and development of chloritoid-bearing eclogitic assemblages in subcontinental metagabbro (Sesia–Lanzo zone, Italy)

In the coronitic metagabbroic rocks of the Corio and Monastero metagabbro bodies in the continental Sesia–Lanzo zone of the western Italian Alps, a variety of mineral reactions that testify to prograde conditions from greenschist to eclogite-facies can be recognised. A microstructural and microchemical study of a series of samples characterized by coronitic textures and pseudomorphic replacement of the original igneous minerals has allowed the prograde reactions undergone by the rocks to be established.

In completely eclogitized coronitic samples, paragonite, blue amphibole, garnet, epidote, fine grained jadeite and chloritoid occur in plagioclase microdomains (former igneous plagioclase). The mafic mineral microdomains consist of glaucophane and garnet. Complexly-zoned amphiboles constrain changing metamorphic conditions: cores of pre-Alpine brown hornblende and/or tremolite are preserved inside rims of a sodic–calcic amphibole that are in turn surrounded by a sodic amphibole. The main high-pressure mineral assemblage, as seen in mylonites, involves glaucophane, chloritoid, epidote, garnet ± phengite, ± paragonite. Some layers within the gabbro contain garnet, omphacite, ± glaucophane, and acid dykes crosscutting the gabbro body contain jadeite, quartz, garnet, epidote and paragonite.

The presence of chloritoid-bearing high-pressure assemblages reflects hydration of the gabbros during their pre-Alpine exhumation prior to subduction, as well as the composition of the microdomains operating during subduction. The pressure and temperature conditions of gabbro transformation during subduction are inferred to be 450–550 °C at up to 2 GPa on the basis of the chloritoid-bearing assemblages. The factors controlling the reaction pathway to form chloritoid-bearing high-pressure assemblages in mafic rocks are inferred from these observations.     

Petrology of pelitic schists in the oligoclase-biotite zone of the Sanbagawa metamorphic terrain, Japan: phase equilibria in the highest grade zone of a high-pressure intermediate type of metamorphic belt

The oligoclase-biotite zone of the Bessi area, central Shikoku is characterized by sodic plagioclase (X_Ca= 0.10–0.28)-bearing assemblages in pelitic schists, and represents the highest-grade zone of the Sanbagawa metamorphic terrain. Mineral assemblages in pelitic schists of this zone, all with quartz, sodic plagioclase, muscovite and clinozoisite (or zoisite), are garnet + biotite + chlorite + paragonite, garnet + biotite + hornblende + chlorite, and partial assemblages of these two types. Correlations between mineral compositions, mineral assemblages and mineral stability data assuming PH₂O = P_solid suggests that metamorphic conditions of this zone are about 610 ± 25°C and 10 ± 1 kbar.
Based upon a comparative study of mineralogy and chemistry of pelitic schists in the oligoclase-biotite zone of the Sanbagawa terrain with those in the New Caledonia omphacite zone as an example of a typical high-pressure type of metamorphic belt and with those in a generalized'upper staurolite zone'as an example of a medium-pressure type of metamorphic belt, progressive assemblages within these three zones can be related by reactions such as:     

From granulites to eclogites in the Sesia zone (Italian Western Alps): a record of the opening and closure of the Piedmont ocean

The Sesia zone (Italian Western Alps) offers one of the best preserved examples of pre-Alpine basement reactivated, under eclogite facies conditions, during the Alpine orogenesis. A detailed mineralogical study of eclogitized acid and basic granulites, and related amphibolites, is presented. In these rare weak to undeformed rocks microstructural investigations allow three main metamorphic stages to be distinguished.
(a) A medium- to low- P granulite stage giving rise to the development of orthopyroxene + garnet + plagioclase + brown amphibole + ilmenite ± biotite in basic granulites and garnet + K-feldspar + plagioclase + cordierite + sillimanite + biotite + ilmenite in acid granulites.
(b) A post-granulite re-equilibration, associated with the development of shear zones, producing discrete amphibolitization of the basic granulites and widespread development of biotite + sillimanite + cordierite + spinel in the acid rocks.
(c) An eo-Alpine eclogite stage giving rise to the crystallization of high- P and low- T assemblages.
In an effort to quantify this evolution, independent well-calibrated thermobarometers were applied to basic and acid rocks. For the granulite event, P-T estimates are 7–9 kbar and 700–800° C, and for subsequent retrograde evolution, P-T was 4–5 kbar and 600° C. For the eo-Alpine eclogite metamorphism, pressure and temperature conditions were 14–16 kbar and 550° C.
The inferred P-T path is consistent with an uplift of continental crust produced by crustal thinning prior to the subduction of the continental rocks. In the light of the available geochronological constraints we propose to relate the pre-Alpine granulite and post-granulite retrograde evolution to the Permo-Jurassic extensional regime. The complex granulite-eclogite transition is thus regarded as a record of the opening and of the closure of the Piedmont ocean.     

Exsolution of Ca-amphibole from glaucophane and the miscibility gap between sodic and calcic amphiboles

Transmission and analytical electron microscopy (TEM/AEM) of glaucophane from glaucophane + Ca-amphibole-bearing blueschist and eclogite from two Vermont localities (Ecologite Brook and Tillotson Peak) and one California locality (Cazadero) has revealed the first evidence from exsolution for the miscibility gap between sodie and calcic amphiboles. The Tillotson Peak samples and the Cazadero samples contain coarsegrained glaucophane—actinolite pairs, while the Eclogite Brook samples contain coexisting glaucophane and actinolitic hornblende. Ca-rich glaucophanes contain abundant fine-scale lamellae of Ca-rich amphibole. These lamellae are usually oriented near (100) and . High-resolution TEM (HRTEM) images show them to be coherent. The exsolution lamellae are so narrow, beyond the resolution of AEM, that their true Ca contents are obscured by analytical contributions from the surrounding host. The AEM data suggest that the lamellae are either winchite or actinolite, depending on the true Ca concentration. In most cases, the exsolution lamellae have very curved interfaces and show variable orientation. This is attributed to the close similarity of unit-cell parameters for the two amphiboles. Three-dimensional optimal phase-boundary calculations using EPLAG (Fleet 1982) show that the observed 100 and orientations are consistent with the minimization of area strain between the two lattices along the interface. Some samples show evidence for incipient exsolution in the form of homogeneously distributed, fine-scale precipitates. These results suggest that Ca-rich glaucophanes from other glaucophane—actinolite assemblages may be exsolved at the TEM scale. The coexisting amphiboles from Eclogite Brook also have been studied using the electron microprobe (EMP). The compositional gap defined by the Eclogite Brook pairs is consistent with previously reported results, but shows a wider break along the glaucophane—actinolite pseudobinary join, suggesting very limited solid solution up to temper-atures of about 500–550°C. The glaucophanes are relatively poor in Ca, except for one anomalous grain containing Ca-amphibole lamellae. Ferric iron, estimated by normalization to fixed cation numbers, is strongly partitioned into the actinolitic hornblende and the glaucophanes are very poor in the riebeckite component.     

Phase relations in the greenschist-blueschist-amphibolite-eclogite facies in the system Na2O-CaO-FeO-MgO-Al2O3-SiO2-H2O (NCFMASH), with application to metamorphic rocks from Samos, Greece

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     

Phase equilibria in rocks of the paleoproterozoic banded iron formation (BIF) of the Lebedinskoe deposit, Kursk Magnetic Anomaly, and the petrogenesis of BIF with alkali amphiboles

BIF with alkali amphibole at the Lebedinskoe iron deposits, the largest in Russia, were metamorphosed at 550°C and 2–3 kbar and contain ferriwinchite, riebeckite, actinolite, grunerite, and aegirine-augite. All reaction textures observed in the rocks were produced during the prograde metamorphic stage and represent the following succession of mineral replacements: Gru → Rbk, Act → Win → Rbk. Data obtained on the textural relations and compositional variations of Ca, Ca-Na, and Na Al-free amphiboles point to the complete miscibility in the actinolite-ferriwinchite and ferriwinchite-riebeckite isomorphic series. Riebeckite is formed in BIF during the prograde metamorphic stage, with the participation of a fluid insignificantly enriched in Na⁺ and at increasing oxygen fugacity. The critical factors controlling the development of alkali amphiboles and Ca-Na pyroxenes in carbonate-bearing BIF is the oxygen activity and the presence of at least low concentrations of Na⁺ ions in the fluid. The minerals contain Fe³⁺, and all reactions producing them are oxidation reactions. The origin of riebeckite late in the course of the mineral-forming process is caused by the Ca²⁺Mg²⁺ → Na⁺Fe³⁺ heterovalent isomorphic replacement in calcic and calcic-sodic amphiboles and by the oxidation of grunerite in the presence of a fluid enriched in Na ions.     

Amphibolitization of metagabbros in the Scottish Highlands

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 (Al^vi+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.     

Metamorphic evolution of the Naga Hills eclogite and blueschist, Northeast India: implications for early subduction of the Indian plate under the Burma microplate

Tectonic slices and lenses of eclogite within mafic and ultramafic rocks of the Early Cretaceous–Eocene Naga Hills ophiolite were studied to constrain the physical conditions of eastward subduction of the Indian plate under the Burma microplate and convergence rate prior to the India–Eurasia collision. Some of the lenses are composed of eclogite, garnet-blueschist, glaucophanite and greenschist from core to margin, representing a retrograde hydrothermal alteration sequence. Barroisite, garnet, omphacite and epidote with minor chlorite, phengite, rutile and quartz constitute the peak metamorphic assemblage. In eclogite and garnet-blueschist, garnet shows an increase in Mg and Fe and decrease in Mn from core to rim. In chlorite in eclogite, Mg increases from core to rim. Inclusions of epidote, glaucophane, omphacite and quartz in garnet represent the pre-peak assemblage. Glaucophane also occurs profusely at the rims of barroisite. The matrix glaucophane and epidote represent the post-peak assemblage. The Fe³⁺ content of garnet-hosted omphacite is higher than that of matrix omphacite, and Fe³⁺ increases from core to rim in matrix glaucophane. Albite occurs in late stage veins. P – T pseudosection analysis indicates that the Naga Hills eclogites followed a clockwise P – T path with prograde metamorphism beginning at ∼1.3 GPa/525 °C and peaking at 1.7–2.0 GPa/580–610 °C, and subsequent retrogression to ∼1.1 GPa/540 °C. A comparison of these P – T conditions with numerical thermal models of plate subduction indicates that the Naga Hills eclogites probably formed near the top of the subducting crust with convergence rates of ∼ 55–100 km Myr⁻¹, consistent with high pre-collision convergence rates between India and Eurasia.     

Amphibole evolution in Variscan eclogite-amphibolites from the Savona crystalline massif (Western Ligurian Alps, Italy): Controls on the decompressional P-T-t path

The Variscan metamorphic evolution of eclogite-amphibolites from the Savona Crystalline Massif is marked by the occurence of calcic amphiboles. Microtextural relations together with coupled electron microprobe and X-ray investigations on amphiboles pointed out a complex decompressional evolution.

A prograde stage of the evolution in the eclogite facies (temperature conditions estimated as ca. 620°C) is recorded by compositional zoning and inclusions in garnet. The eclogitic event (pressure conditions 12kbar) produced assemblages of garnet, omphacite, Ca-amphibole, zoisite, quartz and rutile. Composition and zoning of matrix eclogitic amphiboles reveal that the subsequent evolution in the eclogite facies contemplates a late re-equilibration under lower conditions of temperature (ca. 540°C) and pressure. The eclogitic amphiboles are pargasitic to edenitic hornblendes, and are marked by rather high Na contents at the M4 site (up to 0.5 apfu).

The forming of coarse-grained diopside-plagioclase symplectites and of amphibole-plagioclase coronas represent the early results of the destabilization of omphacites and garnets in the amphibolite facies. Pressure conditions of this stage have been estimated of ca. 10 kbar, while temperature conditions are poorly constrained. However, the increase in edenite (NaAlSi₋₁) at the outermost rims of the matrix eclogitic amphiboles and the very high values of edenite and tschermack (Al₂Mg₋₁Si₋₁) components in the coronitic amphiboles (subsilicic pargasites) suggest that temperature increase accompanied the early decompression to the amphibolite facies.

Subsequent retrogression in the low-grade amphibolite facies resulted in the complete breakdown of omphacite, producing finer-grained symplectites. This stage is also recorded by the amphibole growth (magnesio-hornblendes to edenitic hornblendes with negligible Na amounts at the M4 site) at the expense of the clinopyroxene symplectites and as outward rims around the coronitic amphiboles.

Frequently, amphibolites are completely recrystallized and do not retain any relic of high pressure assemblages. Temperature conditions for this late amphibolitic event have been estimated of ca. 510°C, while pressure conditions are inferred in the range 4–7 kbar.

Such a complicated decompressional evolution is indicative of complex uplift tectonics after a subduction event.     

Coexisting Amphiboles from Blueschist Facies Metamorphic Rocks

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.     

A new petrogenetic grid for low-grade metabasites

Abstract We have used internally-consistent thermodynamic data to present calculated phase equilibria for the system Na₂O-CaO-MgO-Al₂O₃-SiO₂-H₂O (NCMASH), in the range 0–500° C and 0.1–10 kbar, involving the phases anorthite, glaucophane, grossular, heulandite, jadeite, laumontite, lawsonite, paragonite, prehnite, pumpellyite, stilbite, tremolite, wairakite, zoisite with excess albite, clinochlore, quartz and pure water. Average activity terms derived from published mineral chemical data were included for clinochlore, glaucophane, prehnite, pumpellyite, tremolite, and zoisite. The new petrogenetic grid delineates stability fields and parageneses of common index minerals in zeolite, prehniteactinolite, prehnite-pumpellyite, pumpellyite-actinolite, blueschist and greenschist facies metabasites. The stability fields of mineral assemblages containing prehnite, pumpellyite, epidote, actinolite (+ albite + chlorite + quartz) were analysed in some detail, using activity data calculated from five specific samples. For example, the prehnite-actinolite facies covers a P-T field ranging from about 220 to 320° C at pressures below 4.5 kbar. The transition from the prehnite-actinolite and pumpellyite-actinolite to greenschist facies occurs at about 250–300° C at 1–3 kbar and at about 250–350° C at 3–8 kbar. P-T fields of individual facies overlap considerably due to variations in chemical composition.     

P-T-X (CO2) conditions in mafic and calc-silicate hornfelses from Oberon, New South Wales, Australia

Abstract The Rockley Volcanics from near Oberon, New South Wales occur within the aureole of the Carboniferous Bathurst Batholith and have been contact metamorphosed at P ∼ 100 ± 50MPa (10.5kbar) and a maximum T ∼ 565°C in the presence of a C–O–H fluid. Prior to contact metamorphism the volcanics were regionally metamorphosed and altered with the extensive development of actinolite, chlorite, plagioclase, quartz and calcite. The contact metamorphosed equivalents of these rocks have been subdivided into: Ca-poor (cordierite + gedrite), Mg-rich (amphibole + olivine + spinel), mafic (amphibole + plagioclase) and Ca-rich (amphibole + garnet + diopside; diopside + plagioclase; garnet + diopside + wollastonite) rocks.
The chemistry of the minerals in the hornfelses was controlled by the bulk rock chemistry and fluid composition. Pargasites and hastingsites as well as an unusual phlogopite with blue green pleochroism, are found in Ca-rich hornfelses. A comparison of the assemblages with experimentally derived equilibria suggests that the fluid phase associated with the Ca-rich hornfelses was water-rich (X_co2= 0.1 to 0.3) while that associated with the Mg-rich hornfelses was enriched in CO₂ (X_co2 > 0.7). The different hornfels types have reacted to contact metamorphism independently in both their solid and fluid chemistries.