Jadeite–garnet glaucophane schists in the Bizan area,Sambagawa metamorphic belt,eastern Shikoku,Japan: significance and extent of eclogite facies metamorphism

Eclogite facies metamorphic rocks have been discovered from the Bizan area of eastern Shikoku, Sambagawa metamorphic belt. The eclogitic jadeite–garnet glaucophane schists occur as lenticular or sheet‐like bodies in the pelitic schist matrix, with the peak mineral assemblage of garnet + glaucophane + jadeite + phengite + quartz. The jadeitic clinopyroxene (X_Jd 0.46–0.75) is found exclusively as inclusions in porphyroblastic garnet. The eclogite metamorphism is characterized by prograde development from epidote–blueschist to eclogite facies. Metamorphic P–T conditions estimated using pseudosection modelling are 580–600 °C and 18–20 kbar for eclogite facies. Compared with common mafic eclogites, the jadeite–garnet glaucophane schists have low CaO (4.4–4.5 wt%) and MgO (2.1–2.3 wt%) bulk‐rock compositions. The P–T– pseudosections show that low X_Ca bulk‐rock compositions favour the appearance of jadeite instead of omphacite under eclogite facies conditions. This is a unique example of low X_Ca bulk‐rock composition triggered to form jadeite at eclogite facies conditions. Two significant types of eclogitic metamorphism have been distinguished in the Sambagawa metamorphic belt, that is, a low‐T type and subsequent high‐T type eclogitic metamorphic events. The jadeite–garnet glaucophane schists experienced low‐T type eclogite facies metamorphism, and the P–T path is similar to lawsonite‐bearing eclogites recently reported from the Kotsu area in eastern Shikoku. During subduction of the oceanic plate (Izanagi plate), the hangingwall cooled gradually, and the geothermal gradient along the subduction zone progressively decreased and formed low‐T type eclogitic metamorphic rocks. A subsequent warm subduction event associated with an approaching spreading ridge caused the high‐T type eclogitic metamorphism within a single subduction zone.     

Petrogenesis and implications of jadeite‐bearing kyanite eclogite from the Sanbagawa belt (SW Japan)

Jadeite‐bearing kyanite eclogite has been discovered in the Iratsu body of the Sanbagawa belt, SW Japan. The jadeite + kyanite assemblage is stable at higher pressure–temperature (P–T) conditions or lower H₂O activity [a(H₂O)] than paragonite, although paragonite‐bearing eclogite is common in the Sanbagawa belt. The newly discovered eclogite is a massive metagabbro with the peak‐P assemblage garnet + omphacite + jadeite + kyanite + phengite + quartz + rutile. Impure jadeite is exclusively present as inclusions in garnet. The compositional gap between the coexisting omphacite (P2/n) and impure jadeite (C2/c) suggests relatively low metamorphic temperatures of 510–620 °C. Multi‐equilibrium thermobarometry for the assemblage garnet + omphacite + kyanite + phengite + quartz gives peak‐P conditions of ~2.5 GPa, 570 °C. Crystallization of jadeite in the metagabbro is attributed to Na‐ and Al‐rich effective bulk composition due to the persistence of relict Ca‐rich clinopyroxene at the peak‐P stage. By subtracting relict clinopyroxene from the whole‐rock composition, pseudosection modelling satisfactorily reproduces the observed jadeite‐bearing assemblage and mineral compositions at ~2.4–2.5 GPa, 570–610 °C and a(H₂O) >0.6. The relatively high pressure conditions derived from the jadeite‐bearing kyanite eclogite are further supported by high residual pressures of quartz inclusions in garnet. The maximum depth of exhumation in the Sanbagawa belt (~80 km) suggests decoupling of the slab–mantle wedge interface at this depth.     

Separate or shared metamorphic histories of eclogites and surrounding rocks? An example from the Bohemian Massif

Eclogite boudins occur within an orthogneiss sheet enclosed in a Barrovian metapelite‐dominated volcano‐sedimentary sequence within the Velké Vrbno unit, NE Bohemian Massif. A metamorphic and lithological break defines the base of the eclogite‐bearing orthogneiss nappe, with a structurally lower sequence without eclogite exposed in a tectonic window. The typical assemblage of the structurally upper metapelites is garnet–staurolite–kyanite–biotite–plagioclase–muscovite–quartz–ilmenite ± rutile ± silli‐manite and prograde‐zoned garnet includes chloritoid–chlorite–paragonite–margarite, staurolite–chlorite–paragonite–margarite and kyanite–chlorite–rutile. In pseudosection modelling in the system Na₂O–CaO–K₂O–FeO–MgO–Al₂O₃–SiO₂–H₂O (NCKFMASH) using THERMOCALC, the prograde path crosses the discontinuous reaction chloritoid + margarite = chlorite + garnet + staurolite + paragonite (with muscovite + quartz + H₂O) at 9.5 kbar and 570 °C and the metamorphic peak is reached at 11 kbar and 640 °C. Decompression through about 7 kbar is indicated by sillimanite and biotite growing at the expense of garnet. In the tectonic window, the structurally lower metapelites (garnet–staurolite–biotite–muscovite–quartz ± plagioclase ± sillimanite ± kyanite) and amphibolites (garnet–amphibole–plagioclase ± epidote) indicate a metamorphic peak of 10 kbar at 620 °C and 11 kbar and 610–660 °C, respectively, that is consistent with the other metapelites. The eclogites are composed of garnet, omphacite relicts (jadeite = 33%) within plagioclase–clinopyroxene symplectites, epidote and late amphibole–plagioclase domains. Garnet commonly includes rutile–quartz–epidote ± clinopyroxene (jadeite = 43%) ± magnetite ± amphibole and its growth zoning is compatible in the pseudosection with burial under H₂O‐undersaturated conditions to 18 kbar and 680 °C. Plagioclase + amphibole replaces garnet within foliated boudin margins and results in the assemblage epidote–amphibole–plagioclase indicating that decompression occurred under decreasing temperature into garnet‐free epidote–amphibolite facies conditions. The prograde path of eclogites and metapelites up to the metamorphic peak cannot be shared, being along different geothermal gradients, of about 11 and 17 °C km^?1, respectively, to metamorphic pressure peaks that are 6–7 kbar apart. The eclogite–orthogneiss sheet docked with metapelites at about 11 kbar and 650 °C, and from this depth the exhumation of the pile is shared.     

Coexistence of garnet blueschist and eclogite in South Tianshan,NW China: dependence of P–T evolution and bulk‐rock composition

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 + FeO_total + 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 P_max to the T_max stage and a post‐T_max decompression with slightly cooling stage, and similar P–T conditions at the T_max stage. The post‐T_max 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.     

The Effects of Disequilibrium and Deformation on the Mineralogical Evolution of Quartz Diorite During Metamorphism in the Eclogite Facies

In the Sesia Zone, Western Alps, a large volume of orthogneissformed as a result of eclogite fades metamorphism and deformationof quartz diorite during early Alpine underthrusting and subduction.Rare lenses of undeformed metaquartz diorite, preserved withinthe orthogneiss, represent an early stage in the evolution ofthis latter rock type. The metamorphic and microstructural evolutionof the orthogneiss in the eclogite fades has been reconstructedfrom studies of gradational contacts between undeformed andstrongly deformed rocks. High pressure transformations of the original igneous plagioclase+ biotite + quartz assemblage to jadeitic pyroxene (Jd_{0.95 –0.85}+ zoisite + quartz + garnet + 2 muscovites developed prior todeformation. Slow intergranular diffusion resulted in a stateof disequilibrium between small textural domains in the metaquartzdiorite. The compositions of the phases of the undeformed metaquartzdiorite do not reflect the bulk rock composition, but were controlledby their position relative to reactant phases. The jadeiticpyroxenes, for example, formed in localized domains which originallyconsisted of sodic plagioclase whereas omphacite was the equilibriumpyroxene for the bulk rock composition. Mineralogical changes which occurred during subsequent deformationof the metaquartz diorite are interpreted as resulting froma progressive enlargement of equilibrium domains and the partialequilibration of mineral compositions to the bulk rock compositionrather than from changes in pressure and temperature. Initiallyduring high-strain deformation, fine-grained aggregates of jadeiticpyroxene + quartz + zoisite (originally pseudomorphing plagioclase)are inferred to have deformed by a mechanism of grain boundarysliding accommodated by diffusive mass transfer. Muscovite andgarnet compositions homogenized during the deformation but dueto slow intracrystalline diffusion, pyroxene compositions (Jd_0.95–0.80) remained metastable. The coarsening of pyroxeneeventually terminated deformation by grain boundary slidingand this mineral subsequently deformed by intracrystalline plastidty.This latter process was accompanied by and perhaps catalyseda change in pyroxene composition from metastable jadeite towardsomphacite by a reaction involving the resorption of garnet andthe nucleation and growth of paragonite. The resulting orthogneissconsists of quartz + omphadte + garnet + phengite + paragonite+ zoisite. The rock is characterized by a broad range of pyroxenecompositions (Jd_{0.8 –0.5}) due to the incomplete equilibrationof this mineral to the bulk rock composition and a lack of Fe-Mgexchange equilibrium between pyroxene and garnet. However, incontrast to the undeformed metaquartz diorite, there are noobvious textural indications of disequilibrium between phasesin the orthogneiss     

Metamorphic evolution of low-T eclogite from the North Qilian orogen, NW China: evidence from petrology and calculated phase equilibria in the system NCKFMASHO

Low‐T eclogites in the North Qilian orogen, NW China share a common assemblage of garnet, omphacite, glaucophane, epidote, phengite, quartz and rutile with or without paragonite. Phase relations for the low‐T eclogites can be modelled well in the system NCKFMASHO with the updated solid‐solution models for amphibole and clinopyroxene. Garnet in the eclogite typically exhibits growth zonations in which pyrope increases while grossular somewhat decreases from core to rim, which is modelled as having formed mainly in the P–T conditions of lawsonite‐eclogite facies at the pre‐peak stage. Omphacite shows an increase in jadeite component as aegirine and also total FeO decrease in going from the inclusions in garnet to grains in the matrix, and from core to rim of zoned crystals, reflecting an increase in metamorphic P–T conditions. Glaucophane exhibits a compositional variation in X(gl) (= Fe²⁺/(Fe²⁺ + Mg)) and F(gl) (= Fe³⁺/(Fe³⁺ + Al) in M2 site), which decrease from the inclusions in garnet to crystals in the matrix, consistent with an increase in P–T conditions. However, for zoned matrix crystals, the X(gl) and F(gl) increase from core to rim, is interpreted to reflect a late‐stage decompression. Using composition isopleths for garnet rim and phengite in P–T pseudosections, peak P–T conditions for three samples Q5–45, Q5–01 and Q7–28 were estimated as 530–540 °C at 2.10–2.25 GPa, 580–590 °C at 2.30–2.45 GPa and 575–590 °C at 2.50–2.65 GPa, respectively, for the same assemblage garnet + omphacite + glaucophane + lawsonite (+ phengite + quartz + rutile) at the peak stage. The eclogites suggest similar P–T ranges to their surrounding felsic–pelitic schists. During post‐peak decompression of the eclogites, the most distinctive change involves the transformation of lawsonite to epidote, releasing large amount of water in the rock. The released fluid promoted further growth of glaucophane at the expense of omphacite and, in appropriate bulk‐rock compositions, paragonite formed. The decompression of eclogite did not lead to pronounced changes in garnet and phengite compositions. Peak P–T conditions of the North Qilian eclogite are well constrained using both the average P–T and pseudosection approaches in Thermocalc. Generally, the conventional garnet–clinopyroxene geothermometer is too sensitive to be used for constraining the temperature of low‐T eclogite because of the uncertainty in Fe³⁺ determination in omphacite and slight variations in mineral compositions because of incomplete equilibration.     

Dehydration of metapelites during high‐P metamorphism: The coupling between fluid sources and fluid sinks

Polymetamorphic metapelites and embedded eclogites share a complex, episodic interplay of dehydration and fluid infiltration at the eclogite type‐locality (Saualpe–Koralpe, Eastern Alps, Austria). The metapelites inherited a fluid content (i.e. mineral‐bound OH expressed in terms of mol.% H₂O) of ～6–7 mol.% H₂O from high‐T–low‐P metamorphism experienced during the Permian. At or near P_max of the subsequent Eoalpine event (～20 kbar and 680^°C), the breakdown of paragonite to Na‐rich clinopyroxene and kyanite in metapelites released a discrete pulse of hydrous fluid. Prior to the dehydration event, the rocks were largely fluid absent, allowing only limited re‐equilibration during the prograde Eoalpine evolution. Similarly, Permian‐aged gabbros have persisted metastably due to the absence of a catalyst prior to fluid‐induced re‐equilibration. The fluid triggered partial to complete eclogitization along a fluid infiltration front partially preserved in metagabbro. Near‐isothermal decompression to ～7.5–10 kbar and 670–690°C took place under fluid‐absent conditions. After decompression, a second breakdown of phengitic white mica and garnet produced muscovite, biotite, plagioclase and ～0.1–0.7 mol.% H₂O that enhanced extensive fluid‐aided re‐equilibration of the metapelites. Potential relicts of high‐P assemblages were largely obliterated and replaced by the recurrent amphibolite facies assemblage garnet+biotite+staurolite+kyanite+muscovite+plagioclase+ilmenite+quartz. The hydrous fluid originating from the metapelites infiltrated the embedded eclogites at these P–T conditions and induced the local breakdown of the peak assemblage omphacite and garnet to fine‐grained symplectites of diopside and plagioclase. Further fluid infiltration led to the formation of hornblende–quartz poikiloblasts at the expense of the symplectites. The metapelites re‐equilibrated until the growth of retrograde staurolite consumed any remaining free fluid, thereby terminating the process. Further re‐equilibration is inhibited by both the lack of a catalytic fluid and H₂O as a reactant essential for rehydration reactions. The interplay between fluid sources and fluid sinks describes a closed cycle for the rocks at the eclogite type‐locality. Final, near‐isobaric cooling is indicated by a slight increase of X_Fe in garnet rims. Post‐decompression dehydration and fluid‐aided re‐equilibration arrested by the introduction of staurolite might explain the apparently homogeneous retrogression conditions as well as the notorious absence of diagnostic high‐P assemblages in metapelites at the eclogite type‐locality.     

Evidence for multiple burial–partial exhumation cycles from the Onodani eclogites in the Sambagawa metamorphic belt,central Shikoku,Japan

Eclogites from the Onodani area in the Sambagawa metamorphic belt of central Shikoku occur as layers or lenticular bodies within basic schists. These eclogites experienced three different metamorphic episodes during multiple burial and exhumation cycles. The early prograde stage of the first metamorphic event is recorded by relict eclogite facies inclusions within garnet cores (X_Sps 0.80–0.24, X_Alm 0–0.47). These inclusions consist of relatively almandine‐rich garnet (X_Sps 0.13–0.24, X_Alm 0.36–0.45), aegirine‐augite/omphacite (X_Jd 0.08–0.28), epidote, amphiboles (e.g. actinolite, winchite, barroisite and taramite), albite, phengite, chlorite, calcite, titanite, hematite and quartz. The garnet cores also contain polyphase inclusions consisting of almandine‐rich garnet, omphacite (X_Jd 0.27–0.28), amphiboles (e.g. actinolite, winchite, barroisite, taramite and katophorite) and phengite. The peak P–T conditions of the first eclogite facies metamorphism are estimated to be 530–590 °C and 19–21 kbar succeeded by retrogression into greenschist facies. The second prograde metamorphism began at greenschist facies conditions. The peak metamorphic conditions are defined by schistosity‐forming omphacites (X_Jd ≤ 49) and garnet rims containing inclusions of barroisitic amphibole, phengite, rutile and quartz. The estimated peak metamorphic conditions are 630–680 °C and 20–22 kbar followed by a clockwise retrograde P–T path with nearly isothermal decompression to 8–12 kbar. In veins cross‐cutting the eclogite schistosity, resorbed barroisite/Mg‐katophorite occurs as inclusions in glaucophane which is zoned to barroisite, suggesting a prograde metamorphism of the third metamorphic event. The peak P–T conditions of this metamorphic event are estimated to be 540–600 °C and 6.5–8 kbar. These metamorphic conditions are correlated with those of the surrounding non‐eclogitic Sambagawa schists. The Onodani eclogites were formed by subduction of an oceanic plate, and metamorphism occurred beneath an accretionary prism. These high‐P/T type metamorphic events took place in a very short time span between 100 and 90 Ma. Plate reconstructions indicate highly oblique subduction of the Izanagi plate beneath the Eurasian continent at a high spreading rate. This probably resulted in multiple burial and exhumation movements of eclogite bodies, causing plural metamorphic events. The eclogite body was juxtaposed with non‐eclogitic Sambagawa schists at glaucophane stability field conditions. The amalgamated metamorphic sequence including the Onodani eclogites were exhumed to shallow crustal/surface levels in early Eocene times (c. 50 Ma).     

Phase Equilibria of Hornblende‐Bearing Eclogite in the Western Dabie Mountain,Central China

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.     

Retrograde replacement of andalusite by Ca–Na mica in chloritoid-bearing metapelites. PTX modelling of rocks with different Al content in the MnNCKFMASH system

Andalusite porphyroblasts are totally pseudomorphosed by margarite–paragonite aggregates in aluminous pelites containing the peak mineral assemblage andalusite, chlorite, chloritoid, margarite, paragonite, quartz ± garnet, in a NW Iberia contact area. Equilibria at low P–T are investigated using new KFMASH and (mainly) MnCNKFMASH grids constructed with Thermocalc 3.21. P–T and T–X pseudosections with phase modal volume isopleths are constructed for compositions relatively richer and poorer in andalusite to model the assemblages in an andalusite‐bearing rock that contains a thin andalusite‐rich band (ARB) during retrogression. Their compositions, prior to retrogression, are used in the modelling, and have been retrieved by restoring the pseudomorph‐forming elements into the current‐depleted matrix, except for Al₂O₃ which is assumed to be immobile. Compositional differences between the thin band and the rest of the rock have not resulted in differences in andalusite porphyroblast retrogression. The absence of chloritoid resorbtion implies either a pressure increase at constant reacting‐system composition, or that its composition changed during retrogression at constant pressure, by becoming enriched in the progressively replaced andalusite porphyroblasts. T–X pseudosections at 1 kbar model this latter process using as end‐members in X, first, the restored original rock and ARB compositions, and, then the same process, taking into account the change in composition of both as retrogression proceeded. The MnNCKFMASH pseudosections of rocks with different Al contents facilitate making further deductions on the rock‐composition control of the resulting assemblages upon retrogression. Andalusite eventually disappears in relatively Al‐poor rocks, resulting, as in this study, in a rock formed by chloritoid–chlorite as the only FM minerals, plus margarite–paragonite pseudomorphs of andalusite. In rocks richer in Al, chlorite would progressively disappear and a kyanite/andalusite–chloritoid assemblage would eventually be stable at retrograde conditions. The Al‐silicate, stable during retrogression in Al‐rich rocks, indicates pressure conditions and hence the tectonic context under which retrogression took place.     

An investigation of the relationship between bulk composition, inferred reaction progress and fluid-flow parameters for layered micaceous carbonates from Maine, USA

Reaction progress exhibited by multivariant assemblages in micaceous limestones can provide an excellent record of metamorphic fluid flow. However, it is necessary to understand the sensitivity of these assemblages to bulk‐composition parameters. Here, analysis of bulk composition on different scales and pseudosection construction are used to draw conclusions on relationships between bulk composition, fluid flow and reaction progress. Issues addressed include the effects of bulk composition on the mineralogical evolution of micaceous carbonates, the sensitivity of bulk composition to bulk‐composition sampling methods, the magnitude of cross‐layer fluid‐composition gradients, the potential for metasomatism to drive reaction progress, and the relative timing of reaction in adjacent layers. Pseudosections successfully represent observed mineral assemblages, constrain the position of reactions in T–X(CO₂) space, and allow assessment of the sensitivity of reaction position, inferred reaction progress and calculated fluid fluxes to uncertainties in bulk composition. The scale of bulk‐composition sampling affects bulk compositions, calculated modes, predicted mineral assemblages and calculated fluid compositions. Larger samples record an average of different lithological subdomains, while point‐count‐derived bulk compositions are subject to uncertainties related to the small number of sample points. The optimum bulk composition for pseudosection purposes probably lies between measured bulk compositions. Results suggest that reaction progress in some extensively reacted layers was driven by infiltration of H₂O‐rich fluid which flowed or diffused parallel to layering, perpendicular to layering in response to fluid‐composition gradients, and out of veins. Small variations in fluid composition across layering (ΔX(CO₂) < 0.02) were maintained by internal buffering by the mineral assemblages. Internal buffering must also have driven samples up a sequence of narrow low‐variance fields in T–X(CO₂) space, and so reaction in adjacent layers must have close to simultaneous. Metasomatic effects on reaction progress are likely to have been small, so long as the porosity was low.     

Calculated phase equilibria for MORB compositions: a reappraisal of the metamorphic evolution of lawsonite eclogite

Pseudosections calculated with thermocalc predict that lawsonite‐bearing assemblages, including lawsonite eclogite, will be common for subducted oceanic crust that experiences cool, fluid‐saturated conditions. For glaucophane–lawsonite eclogite facies conditions (500–600 °C and 18–28 kbar), MORB compositions are predicted in the NCKMnFMASHO system to contain glaucophane, garnet, omphacite, lawsonite, phengite and quartz, with chlorite at lower temperature and talc at higher temperature. In these assemblages, the pyrope content in garnet is mostly controlled by variations in temperature, and grossular content is strongly controlled by pressure. The silica content in phengite increases linearly with pressure. As the P–T conditions for these given isopleths are only subtly affected by common variations in bulk‐rock compositions, the P–T pseudosections potentially present a robust geothermobarometric method for natural glaucophane‐bearing eclogites. Thermobarometric results recovered both by isopleth and conventional approaches indicate that most natural glaucophane–lawsonite eclogites (Type‐L) and glaucophane–epidote eclogites (Type‐E) record similar peak P–T conditions within the lawsonite stability field. Decompression from conditions appropriate for lawsonite stability should result in epidote‐bearing assemblages through dehydration reactions controlled by lawsonite + omphacite = glaucophane + epidote + H₂O. Lawsonite and omphacite breakdown will be accompanied by the release of a large amount of bound fluid, such that eclogite assemblages are variably recrystallized to glaucophane‐rich blueschist. Calculated pseudosections indicate that eclogite assemblages form most readily in Ca‐rich rocks and blueschist assemblages most readily in Ca‐poor rocks. This distinction in bulk‐rock composition can account for the co‐existence of low‐T eclogite and blueschist in high‐pressure terranes.     

Petrology of very-high-pressure eclogitic rocks from the Brossasco-Isasca Complex, Dora-Maira Massif, Italian Western Alps

Petrographical and mineral chemical data are given for the eclogites which occur in the garnet-kyanite micaschists of the Penninic Dora-Maira Massif between Brossasco, Isasca and Martiniana (Italian Western Alps) and for a sodic whiteschist associated with the pyrope-coesite whiteschists of Martiniana. The Brossasco-Isasca (BI) eclogites are fine grained, foliated and often mica-rich rocks with a strong preferred orientation of omphacite crystals and white micas. Porphyroblasts of hornblende are common in some varieties, whilst zoisite and kyanite occur occasionally in pale green varieties associated with leucocratic layers with quartz, jadeite and garnet. These features differentiate the BI eclogites from the eclogites that occur in other continental units of the Western Alps, which all belong to type C. Garnet, sodic pyroxene and glaucophane are the major minerals in the sodic whiteschist. Sodic pyroxene in the eclogites is an omphacite often close to Jd₅₀Di₅₀, with very little acmite and virtually no Al^IV, and impure jadeite in the leucocratic layers and in the sodic whiteschist. Garnet is almandine with 20–30 mol. % for each of the pyrope and grossular components in the eclogites and a pyrope-rich variety in the sodic whiteschist. White mica is a variably substituted phengite, and paragonite apparently only occurs as a replacement product of kyanite. Amphibole is hornblende in the eclogites, but the most magnesian glaucophane yet described in the sodic whiteschist. Quartz pseudomorphs of coesite were found occasionally in a few pyroxenes and garnets. The P-T conditions during the VHP event are constrained in the eclogites by reactions which define a field ranging from 27–28 kbar to 35 kbar and from 680 to 750° C. These temperatures are consistent with the results of garnet-pyroxene and garnet-phengite geothermometry which suggest that the eclogites may have equilibrated at around 700° C. In the sodic whiteschist pressures ranging from 29 to 35 kbar can be deduced from the stability of the jadeite-pyrope garnet-glaucophane compatibility. As in the eclogites water activity must have been low. Such conditions are close to the P-T values estimated for the early Alpine recrystallization of the pyrope-coesite rock and, like petrographical and mineralogical features, set aside the BI eclogites from the other eclogites of the Western Alps, instead indicating a close similarity to some of the eclogite bodies occurring in the Adula nappe of the Central Alps. An important corollary is that glaucophane stability, at least in Na- and Mg-rich compositions and under very high pressures, may extend up to 700° C, in agreement with the HT stability limit suggested by experimental studies.     

Metamorphism of ultrahigh‐pressure eclogites from the Kebuerte Valley,South Tianshan,NW China: phase equilibria and P–T path

Eclogites from the Kebuerte Valley, Chinese South Tianshan, consist of garnet, omphacite, phengite, paragonite, glaucophane, hornblendic amphibole, epidote, quartz and accessory rutile, titanite, apatite and carbonate minerals with occasional presence of coesite or quartz pseudomorphs after coesite. The eclogites are grouped into two: type I contains porphyroblastic garnet, epidote, paragonite and glaucophane in a matrix dominated by omphacite where the proportion of omphacite and garnet is >50 vol.%; and type II contains porphyroblastic epidote in a matrix consisting mainly of fine‐grained garnet, omphacite and glaucophane where the proportion of omphacite and garnet is <50 vol.%. Garnet in both types of eclogites mostly exhibits core–rim zoning with increasing grossular (X_gr) and pyrope (X_py) contents, but a few porphyroblastic garnet grains in type I eclogite shows core–mantle zoning with increasing X_py and a slight decrease in X_gr, and mantle–rim zoning with increases in both X_gr and X_py. Garnet rims in type I eclogite have higher X_py than in type II. Petrographic observations and phase equilibria modelling with pseudosections calculated using thermocalc in the NCKMnFMASHO system for three representative samples suggest that the eclogites have experienced four stages of metamorphism: stage I is the pre‐peak temperature prograde heating to the pressure peak (P_max) which was recognized by the garnet core–mantle zoning with increasing X_py and decreasing X_gr. The P–T conditions at P_max constrained from garnet mantle or core compositions with minimum X_gr content are 29–30 kbar at 526–540 °C for type I and 28.2 kbar at 518 °C for type II, suggesting an apparent thermal gradient of ～5.5 °C km^?1. Stage II is the post‐P_max decompression and heating to the temperature peak (T_max), which was modelled from the garnet zoning with increasing X_gr and X_py contents. The P–T conditions at T_max, defined using the garnet rim compositions with maximum X_py content and the Si content in phengite, are 24–27 kbar at 590 °C for type I and 22 kbar at 540 °C for type II. Stage III is the post‐T_max isothermal decompression characterized by the decomposition of lawsonite, which may have resulted in the release of a large amount of fluid bound in the rocks, leading to the formation of epidote, paragonite and glaucophane porphyroblasts. Stage IV is the late retrograde evolution characterized by the overprint of hornblendic amphibole in eclogite and the occurrence of epidote–amphibole facies mineral assemblages in the margins or in the strongly foliated domains of eclogite blocks due to fluid infiltration. The P–T estimates obtained from conventional garnet–clinopyroxene–phengite thermobarometry for the Tianshan eclogites are roughly consistent with the P–T conditions of stage II at T_max, but with large uncertainties in temperature. On the basis of these metamorphic stages or P–T paths, we reinterpreted that the recently reported zircon U–Pb ages for eclogite may date the T_max stage or the later decompression stage, and the widely distributed (rutile‐bearing) quartz veins in the eclogite terrane may have originated from the lawsonite decomposition during the decompression stage rather than from the transition from blueschist to eclogite as previously proposed.     

Metamorphic evolution of relict lawsonite‐bearing eclogites from the (U) HP metamorphic belt in the Chinese southwestern Tianshan

In the Chinese southwestern Tianshan (U)HP belt, former lawsonite presence has been predicted for many (U)HP metamorphic eclogites, but only a very few lawsonite grains have been found so far. We discovered armoured lawsonite relicts included in quartz, which, on its part, is enclosed in porphyroblastic garnet in an epidote eclogite H711‐14 and a paragonite eclogite H711‐29. H711‐14 is mainly composed of garnet, omphacite, epidote and titanite, with minor quartz, paragonite and secondary barroisite and glaucophane. Coarse‐grained titanite occasionally occurs in millimetre‐wide veins in equilibrium with epidote and omphacite, and relict rutile is only preserved as inclusions in matrix titanite and garnet. H711‐29 shows the mineral assemblage of garnet, omphacite, glaucophane, paragonite, quartz, dolomite, rutile and minor epidote. Dolomite and rutile are commonly rimed by secondary calcite and titanite respectively. Porphyroblastic garnet in both eclogites is compositionally zoned and exhibits an inclusion‐rich core overgrown by an inclusion‐poor rim. Phase equilibria modelling predicts that garnet cores formed at the P‐peak (490–505 °C and 23–25.5 kbar) and coexisted with the lawsonite eclogite facies assemblage of omphacite + glaucophane + lawsonite + quartz. Garnet rims (550–570 °C and ~20 kbar) grew subsequently during a post‐peak epidote eclogite facies metamorphism and coexisted with omphacite + quartz ± glaucophane ± epidote ± paragonite. The results confirm the former presence of a cold subduction zone environment in the Chinese southwestern Tianshan. The P–T evolution of the eclogites is characterized by a clockwise P–T path with a heating stage during early exhumation (thermal relaxation). The preservation of lawsonite in these eclogites is attributed to isolation from the matrix by quartz and rigid garnet, which should be considered as a new type of lawsonite preservation in eclogites. The complete rutile–titanite transition in H711‐14 took place in the epidote eclogite facies stage in the presence of an extremely CO₂‐poor fluid with X(CO₂) [CO₂/(CO₂ + H₂O) in the fluid] <<0.008. In contrast, the incomplete rutile–titanite transition in H711‐29 may have occurred after the epidote eclogite facies stage and the presence of dolomite reflects a higher X(CO₂) (>0.01) in the coexisting fluid at the epidote eclogite facies stage.     

High-pressure eclogites in northern Jiangsu – southern Shandong province, eastern China

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.     

Isograds and P–T evolution in the eastern Lepontine Alps (Graubünden, Switzerland)

Reactions producing Al‐rich index minerals in the south‐eastern part of the Lepontine Dome (Central Alps, Switzerland) are investigated using mineral distribution maps, microstructural observations and equilibrium phase diagrams. The apparent staurolite mineral zone boundary corresponds to the paragonite breakdown reaction Pg + Grt + Qtz = Pl + Al₂O₃ + W. Equilibrium phase diagrams show that most natural metapelites do not contain staurolite or alumosilicates as long as univalent cations are predominantly accommodated in white mica. For a wide range of metapelitic compositions the paragonite breakdown releases sufficient Al for the formation of these minerals. Rare occurrences of staurolite and kyanite, north of the formerly mapped mineral zone boundaries, coexist with paragonite and are restricted to extremely Al‐rich bulk compositions. The stable branch of the kyanite‐forming paragonite breakdown reaction above 660 °C yields an additional mapable isograd. The second set of Al‐releasing reactions is biotite‐producing phengite breakdown. However, these reactions are less suitable to produce well defined reaction isograds in the field as they are more continuous and their progress is strongly dependent on bulk composition. Well developed fibrolite in metapelites does not appear until staurolite starts to breakdown. We conclude that amphibolite facies conditions in the study area were attained by decompression, without substantial heating at low pressures.     

Experimental study of metamorphic reactions and dehydration processes at the blueschist–eclogite transition during warm subduction

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#=Fe_total/(Fe_total+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.     

Calculated phase equilibria for low- and medium-pressure metapelites in the KFMASH and KMnFMASH systems

Petrogenetic grids in the KFMASH and KMnFMASH model systems calculated with the software thermocalc 3.1 are presented for the P–T range 0.5–12 kbar and 450–900 °C, for assemblages involving garnet, muscovite, chloritoid, biotite, chlorite, staurolite, cordierite, spinel, orthopyroxene, K‐feldspar, Al₂SiO₅ phases, quartz, water and melt. Based on calculated compatibility diagrams and P–T and T–M_Mn [Mn/(Mg + Fe + Mn)] pseudosections for different metapelitic bulk compositions, the principal conclusions are that the addition of Mn to the KFMASH system: (i) enhances the stability of garnet, and, to a lesser extent, aluminosilicates; (ii) reduces the stability of staurolite, cordierite and, to a lesser extent, chlorite; and (iii) extends the medium pressure stability of muscovite and the low‐P stability field of K‐feldspar. The influence of Mn on individual mineral stabilities is strongly related to rock composition, in particular, to the relative contents of Al₂O₃ and K₂O. For metapelites of a range of compositions and M_Mn values, P–T pseudosections in the KFMASH system, in most cases, do not adequately predict the mineral assemblages observed in natural assemblages under medium and low‐pressure conditions. In contrast, the P–T pseudosections in the KMnFMASH system generally provide more satisfactory results, suggesting that MnO is one of the non‐KFMASH components that should not be neglected in documenting the phase equilibria of medium‐ and low‐P metapelites.     

P–T path of high-pressure/low-temperature rocks and tectonic implications in the western Tianshan Mountains, NW China

The Chinese western Tianshan high-pressure/low-temperature (HP–LT) metamorphic belt, which extends for about 200 km along the South Central Tianshan suture zone, is composed of mainly metabasic blueschists, eclogites and greenschist facies rocks. The metabasic blueschists occur as small discrete blocks, lenses, bands, laminae or thick beds in meta-sedimentary greenschist facies country rocks. Eclogites are intercalated within blueschist layers as lenses, laminae, thick beds or large massive blocks (up to 2 km² in plan view). Metabasic blueschists consist of mainly garnet, sodic amphibole, phengite, paragonite, clinozoisite, epidote, chlorite, albite, accessory titanite and ilmenite. Eclogites are predominantly composed of garnet, omphacite, sodic–calcic amphibole, clinozoisite, phengite, paragonite, quartz with accessory minerals such as rutile, titanite, ilmenite, calcite and apatite. Garnet in eclogite has a composition of 53–79 mol% almandine, 8.5–30 mol% grossular, 5–24 mol% pyrope and 0.6–13 mol% spessartine. Garnet in blueschists shows similar composition. Sodic amphiboles include glaucophane, ferro-glaucophane and crossite, whereas the sodic–calcic amphiboles mainly comprise barroisite and winchite. The jadeite content of omphacite varies from 35–54 mol%. Peak eclogite facies temperatures are estimated as 480–580 °C for a pressure range of 14–21 kbar. The conditions of pre-peak, epidote–blueschist facies metamorphism are estimated to be 350–450 °C and 8–12 kbar. All rock types have experienced a clockwise P–T path through pre-peak lawsonite/epidote-blueschist to eclogite facies conditions. The retrograde part of the P–T path is represented by the transition of epidote-blueschist to greenschist facies conditions. The P–T path indicates that the high-pressure rocks formed in a B-type subduction zone along the northern margin of the Palaeozoic South Tianshan ocean between the Tarim and Yili-central Tianshan plates.