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.     

Blueschist facies metamorphism of peralkaline rhyolites from the Tenda crystalline massif (northern Corsica): evidence for involvement in the Alpine subduction event?

The Tenda crystalline massif (northern Corsica) is a fragment of the western Corsica basement involved in the Alpine orogeny. Rhyolite dykes crosscutting the gabbroic complex of Bocca di Tenda (southern sector of the Tenda crystalline massif) show an unusual metamorphic mineral assemblage, defined by jadeite‐bearing (up to 46 mol percentage) aegirine, riebeckite, celadonite‐rich phengite (Si=3.50–3.65 apfu), quartz, albite and K‐feldspar. Jadeite‐bearing aegirine and riebeckite mostly occur as coronas around jadeite‐free aegirine and arfvedsonite, respectively, which both are relics of igneous origin. This metamorphic assemblage reflects the peralkaline compositions, which are characterised by anomalously high contents of SiO₂ and Na₂O, and negligible CaO and MgO. The evolved rocks of the gabbroic sequence (quartz‐diorites to tonalites) and the surrounding granitoids are characterised by the development of riebeckite/ferroglaucophane, epidote, celadonite‐rich phengite and albite, thus pointing to a metamorphic crystallization in the epidote‐blueschist facies. In all the studied rocks, metamorphic reactions were controlled by fluid‐assisted mass‐transfer through grain boundaries and microfractures. The different mineral assemblages allow the peak P–T metamorphic conditions to be constrained to between 0.8 GPa/300 °C and 1.1 GPa/500 °C. These estimates attest to a geothermal gradient (dT/dP) of 10–13 °C km^?1 and indicate that the Tenda crystalline massif was buried to a minimum depth of 27 km during the Alpine orogeny. The blueschist facies recrystallization in the Tenda crystalline massif has been related to the cessation of an eastward‐dipping subduction event.     

Structure and physical property relations of Mn ilvaite

Structural and compositional data as well as ⁵⁷Fe Mössbauer parameters were determined on a natural Mn-rich monoclinic ilvaite crystal (ideal composition CaFe ₂ ²⁺ Fe³⁺Si₂O₈(OH)) which was used for electrical conductivity and thermopower measurements (part 2 of this paper). A zonar structure was found by electron microprobe analysis with a strong decrease in Mn concentration from the rim to the centre of the crystal in a plane perpendicular to the [001] direction. X-ray powder diffraction analysis of the most Mn-rich composition was performed. Mn²⁺ cations populate preferentially M2 sites of the ilvaite unit cell (space group P21/a), to a lower extent they reside on M1 and a reduced part is on Ca sites. The monoclinic angle was determined to β=90.178(4)°. The structural results are compared to literature data for other natural Mn-rich as well as low-impurity ilvaites; this concerns in particular the lattice b parameter and the undecided issue of the varying β angle. In the literature, the order parameter σ, which describes the varying degree of ordering of Fe²⁺–Fe³⁺ pairs on M11 and M12 sites in chains running parallel to the [001] direction, and structural defects are thought to be related to β. The interrelationship between β and σ with respect to a possible twin domain structure is discussed. Various ⁵⁷Fe Mössbauer spectra were recorded between 151 K and 327 K. Mössbauer parameters and Fe²⁺/Fe³⁺ concentration ratios were determined from the fits to the spectra. Fitting of subspectra was accomplished with the idea to find assignments of Fe²⁺ and Fe³⁺ doublets in agreement with X-ray results. The fraction of Mn²⁺ substituting Fe²⁺ on M1 sites could be estimated.     

Crystal chemistry and reaction relations of piemontites and thulites from highly oxidized low grade metamorphic rocks at Vitali,Andros Island,Greece

Piemontite- and thulite-bearing assemblages from highly oxidized metapelitic and metacalcareous schists associated with braunite quartzites at Vitali, Andros island, Greece, were chemically investigated. The Mn-rich metasediments are intercalated in a series of metapelitic quartzose schists, marbles, and basic metavolcanites which were affected by a regional metamorphism of the highP/T type (T=400–500° C,P>9 kb) and a later Barrovian-type greenschist metamorphism (T=400–500° C,P～-5–6 kb). Texturally and chemically two generations of piemontite (I and II) can be distinguished which may show complex compositional zoning. Piemontite I coexisted at highP/T conditions with braunite, manganian phengite (alurgite), Mn³⁺-Mn²⁺-bearing Na-pyroxene (violan), carbonate, quartz, hollandite, and hematite. Zoned grains generally exhibit a decreasing Mn³⁺ and an increasing Fe³⁺ and Al content towards the rim. Chemical compositions of piemontite I range from 2.0 to 32.1 mole % Mn³⁺, 0 to 25.6 mole % Fe³⁺, and 60.2 to 81.2 mole % Al. Up to 12.5 mole % Ca on the A(2) site can be substituted by Sr. Piemontites formed in contact or close to braunite (±hematite) attained maximum (Mn³⁺+Fe³⁺)Al_?1 substitution corrresponding to about 33 mole % Mn³⁺+Fe³⁺ in lowiron compositions and up to about 39 mole % Mn³⁺+ Fe³⁺ at intermediate Fe³⁺/(Fe³⁺+Mn³⁺) ratios. Piemontite II which discontinuously overgrows piemontite I or occurs as separate grains may have been formed by greenschist facies decomposition of manganian Na-pyroxenes according to the reaction: (1) $$\begin{gathered} {\text{Mn}}^{{\text{3 + }}} - Mn^{2 + } - bearing omphacite/chloromelanite \hfill \\ + CO_2 + H_2 O + HCl \pm hermatite \hfill \\ = piemontite + tremolite + albite + chlorite \hfill \\ + calcite + quartz + NaCl \pm O_2 . \hfill \\ \end{gathered} $$ Thulites crystallized in coexistence with Al-rich piemontite II. All thulites analysed are low-Fe³⁺ manganian orthozoisites with Mn^tot～-Mn³⁺ substituting for Al on the M(3) site. Their compositions range from 2.9 to 7.2 mole % Mn³⁺, 0 to 1.2 mole % Fe³⁺, and 91.8 to 96.7 mole % Al. Piemontites II in thulite-bearing assemblages range from 5.8 to 15.9 mole % Mn³⁺, 0 to 3.7 mole % Fe³⁺, and 83.7 to 93.6 mole % Al. By contrast, piemontites II in thulite-free assemblages are similarly enriched in Mn³⁺ + Fe³⁺ — and partially in Sr²⁺ — as core compositions of piemontite I (21.1 to 29.6 mole % Mn³⁺, 2.0 to 16.5 mole % Fe³⁺, 60.6 to 68.4 mole % Al, 0 to 29.4 mole % Sr in the A(2) site). The analytical data presented in this paper document for the first time a continuous low-Fe³⁺ piemontite solid solution series from 5.8 to 32.1 mole % Mn³⁺. Aluminous piemontite II is enriched by about 3 mole % Mn³⁺+Fe³⁺ relative to coexisting thulite in Fe³⁺-poor samples and by about 6 mole % Mn³⁺+Fe³⁺ in more Fe³⁺-rich samples. Mineral pairs from different samples form a continuous compositional loop. Compositional shift of mineral pairs is attributed to the effect of a variable fluid composition at constantP _fluid andT on the continuous reaction: (2) $$\begin{gathered} piemontite + CO_2 \hfill \\ = thulite + calcite + quartz \hfill \\ + Mn^{2 + } Ca_{ - 1} [calcite] + H{_2} O + O{_2} \hfill \\ \end{gathered} $$ Further evidence for a variable \(x_{H_2 O} \) and/or \(f_{O_2 } \) possibly resulting from fluid infiltration and local buffering during the greenschist metamorphism is derived from the local decomposition of piemontite, braunite, and rutile to form spessartine, calcite, titanite, and hematite by the reactions: (3) $$\begin{gathered} piemontite + braunite + CO_2 \hfill \\ = sperssartine + calcite + quartz \pm hermatite \hfill \\ + H{_2} O + O{_2} \hfill \\ \end{gathered} $$ and more rarely: (4) $$\begin{gathered} piemontite + quartz + rutile + braunite \hfill \\ = spessartine + titanite + hematite + H{_2} O + O{_2} . \hfill \\ \end{gathered} $$      

Petrochemistry and petrology of I-type granitoids in an arc setting: the composite Torul pluton, Eastern Pontides, NE Turkey

The Upper Cretaceous Torul pluton, located in the Eastern Pontides, is of sub-alkaline affinity and displays features typical of volcanic arc granitoids. It is a composite pluton consisting of granodiorite, biotite hornblende monzogranite, quartz monzodiorite, quartz monzonite and hornblende biotite monzogranite. The oldest syenogranite (77.9 ± 0.3 Ma) and the youngest quartz diorite form small stocks within the pluton. Samples from the granodiorites, biotite hornblende monzogranites, quartz monzodiorites, quartz monzonites and hornblende biotite monzogranites have SiO₂ between 57 and 68 wt% and display high-K calc-alkaline, metaluminous to peraluminous characteristics. Chondrite-normalized REE patterns are fractionated (La_cn/Lu_cn = 6.0?14.2) with pronounced negative Eu anomalies (Eu/Eu* = 0.59–0.84). Initial ?_Nd(i) values vary between ?3.1 and ?4.1, initial ⁸⁷Sr/⁸⁶Sr values between 0.7058 and 0.7072, and δ¹⁸O values between +4.4 and +7.3‰. The quartz diorites are characterized by relatively high Mg-number of 36–38, low contents of Na₂O (2.3–2.5 wt%) and SiO₂ (52–55 wt%) and medium-K calc-alkaline, metaluminous composition. Chondrite-normalized REE patterns are relatively flat [(La/Yb)_cn =  2.8–3.3; (Tb/Yb)_cn =  1.2] and show small negative Eu anomalies (Eu/Eu* = 0.74–0.76). Compared to the other rock types, radiogenic isotope signatures of the quartz diorites show higher ⁸⁷Sr/⁸⁶Sr (0.7075–0.7079) and lower ?_Nd(i) (–4.5 to –5.3). The syenogranites have high SiO₂ (70–74 wt%) and display high-K calc-alkaline, peraluminous characteristics. Their REE patterns are characterized by higher La_cn/Lu_cn (12.9) and Eu/Eu* (0.76–0.77) values compared to the quartz diorites. Isotopic signatures of these rocks [?_Nd(i) =  ?4.0 to ?3.3; ⁸⁷Sr/⁸⁶Sr_(i) =  0.7034?0.7060; δ¹⁸ O =  + 4.9 to + 8.2] are largely similar to the other rock types but differ from that of the quartz diorites. Fractionation of plagioclase, hornblende, pyroxene and Fe–Ti oxides played an important role in the evolution of Torul granitoids. The crystallization temperatures of the melts ranged from 800 to 900°C as determined from zircon and apatite saturation thermometry. All these characteristics, combined with low K₂O/Na₂O, low Al₂O₃/(FeO_T + MgO + TiO₂), and low (Na₂O + K₂O)/(FeO_T + MgO + TiO₂) ratios suggest an origin through dehydration melting of mafic lower crustal source rocks.     

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.     

Application of K-feldspar–jadeite–quartz barometry to eclogite facies metagranites and metapelites in the Sesia Lanzo Zone (Western Alps, Italy)*

The eclogite facies assemblage K-feldspar–jadeite–quartz in metagranites and metapelites from the Sesia-Lanzo Zone (Western Alps, Italy) records the equilibration pressure by dilution of the reaction jadeite+quartz=albite. The metapelites show partial transformation from a pre-Alpine assemblage of garnet (Alm₆₃Prp₂₆Grs₁₀)–K-feldspar–plagioclase–biotite±sillimanite to the Eo-Alpine high-pressure assemblage garnet (Alm₅₀Prp₁₄Grs₃₅)–jadeite (Jd_80–97Di_0–4Hd_0–8Acm_0–7)–zoisite–phengite. Plagioclase is replaced by jadeite–zoisite–kyanite–K-feldspar–quartz, and biotite is replaced by garnet–phengite or omphacite–kyanite–phengite. Equilibrium was attained only in local domains in the metapelites and therefore the K-feldspar–jadeite–quartz (KJQ) barometer was applied only to the plagioclase pseudomorphs and K-feldspar domains. The albite content of K-feldspar ranges from 4 to 11 mol% in less equilibrated assemblages from Val Savenca and from 4 to 7 mol% in the partially equilibrated samples from Monte Mucrone and the equilibrated samples from Montestrutto and Tavagnasco. Thermodynamic calculations on the stability of the assemblage K-feldspar–jadeite–quartz using available mixing data for K-feldspar and pyroxene indicate pressures of 15–21 kbar (±1.6–1.9 kbar) at 550±50 °C. This barometer yields direct pressure estimates in high-pressure rocks where pressures are seldom otherwise fixed, although it is sensitive to analytical precision and the choice of thermodynamic mixing model for K-feldspar. Moreover, the KJQ barometer is independent of the ratio PH2O/P_T. The inferred limiting a(H₂O) for the assemblage jadeite–kyanite in the metapelites from Val Savenca is low and varies from 0.2 to 0.6.     

The compositional variation of synthetic sodic amphiboles at high and ultra-high pressures

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

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.     

High-pressure single-crystal X-ray diffraction study of jadeite and kosmochlor

The crystal structures of natural jadeite, NaAlSi₂O₆, and synthetic kosmochlor, NaCrSi₂O₆, were studied at room temperature, under hydrostatic conditions, up to pressures of 30.4 (1) and 40.2 (1) GPa, respectively, using single-crystal synchrotron X-ray diffraction. Pressure–volume data have been fit to a third-order Birch–Murnaghan equation of state yielding V ₀ = 402.5 (4) Å³, K ₀ = 136 (3) GPa, and K ₀ ^′  = 3.3 (2) for jadeite and V ₀ = 420.0 (3) Å³, K ₀ = 123 (2) GPa and K ₀ ^′  = 3.61 (9) for kosmochlor. Both phases exhibit anisotropic compression with unit-strain axial ratios of 1.00:1.95:2.09 for jadeite at 30.4 (1) GPa and 1:00:2.15:2.43 for kosmochlor at 40.2 (1) GPa. Analysis of procrystal electron density distribution shows that the coordination of Na changes from 6 to 8 between 9.28 (Origlieri et al. in Am Mineral 88:1025–1032, 2003) and 18.5 (1) GPa in kosmochlor, which is also marked by a decrease in unit-strain anisotropy. Na in jadeite remains six-coordinated at 21.5 (1) GPa. Structure refinements indicate a change in the compression mechanism of kosmochlor at about 31 GPa in both the kinking of SiO₄ tetrahedral chains and rate of tetrahedral compression. Below 31 GPa, the O3–O3–O3 chain extension angle and Si tetrahedral volume in kosmochlor decrease linearly with pressure, whereas above 31 GPa the kinking ceases and the rate of Si tetrahedral compression increases by greater than a factor of two. No evidence of phase transitions was observed over the studied pressure ranges.     

The crystal chemistry of lithium and Fe3+ in synthetic orthopyroxene

Lithian ferrian enstatite with Li₂O = 1.39 wt% and Fe₂O₃ 7.54 wt% was synthesised in the (MgO–Li₂O–FeO–SiO₂–H₂O) system at P = 0.3 GPa, T = 1,000°C, fO₂ = +2 Pbca, and a = 18.2113(7), b = 8.8172(3), c = 5.2050(2) Å, V = 835.79(9) Å³. The composition of the orthopyroxene was determined combining EMP, LA-ICP-MS and single-crystal XRD analysis, yielding the unit formula ^M2(Mg_0.59Fe _0.21 ²⁺ Li_0.20) ^M1(Mg_0.74Fe _0.20 ³⁺ Fe _0.06 ²⁺ ) Si₂O₆. Structure refinements done on crystals obtained from synthesis runs with variable Mg-content show that the orthopyroxene is virtually constant in composition and hence in structure, whereas coexisting clinopyroxenes occurring both as individual grains or thin rims around the orthopyroxene crystals have variable amounts of Li, Fe³⁺ and Mg contents. Structure refinement shows that Li is ordered at the M2 site and Fe³⁺ is ordered at the M1 site of the orthopyroxene, whereas Mg (and Fe²⁺) distributes over both octahedral sites. The main geometrical variations observed for Li-rich samples are actually due to the presence of Fe³⁺, which affects significantly the geometry of the M1 site; changes in the geometry of the M2 site due to the lower coordination of Li are likely to affect both the degree and the kinetics of the non-convergent Fe²⁺-Mg ordering process in octahedral sites.     

Primary melt from Sannome-gata volcano,NE Japan arc: constraints on generation conditions of rear-arc magmas

The conditions under which rear-arc magmas are generated were estimated using primary basalts from the Sannome-gata volcano, located in the rear of the NE Japan arc. Scoriae from the volcano occur with abundant crustal and mantle xenoliths, suggesting that the magma ascended rapidly from the upper mantle. The scoriae show significant variations in their whole-rock compositions (7.9–11.1 wt% MgO). High-MgO scoriae (MgO > ~9.5 wt%) have mostly homogeneous ⁸⁷Sr/⁸⁶Sr ratios (0.70318–0.70320), whereas low-MgO scoriae (MgO < ~9 wt%) have higher ⁸⁷Sr/⁸⁶Sr ratios (>0.70327); ratios tend to increase with decreasing MgO content. The high-MgO scoriae are aphyric, containing ~5 vol% olivine microphenocrysts with Mg# [100 × Mg/(Mg + Fe²⁺)] of up to 90. In contrast, the low-MgO scoriae have crustal xenocrysts of plagioclase, alkali feldspar, and quartz, and the mineralogic modes correlate negatively with whole-rock MgO content. On the basis of these observations, it is inferred that the high-MgO scoriae represent primary or near-primary melts, while the low-MgO scoriae underwent considerable interaction with the crust. Using thermodynamic analysis of the observed petrological features of the high-MgO scoriae, the eruption temperature of the magmas was constrained to 1,160–1,220 °C. Given that the source mantle was depleted MORB-source mantle, the primary magma was plausibly generated by ~7 % melting of a garnet-bearing spinel peridotite; taking this into consideration, and considering the constraints of multi-component thermodynamics, we estimated that the primary Sannome-gata magma was generated in the source mantle with 0.5–0.6 wt% H₂O at 1,220–1,230 °C and at ~1.8 GPa, and that the H₂O content of the primary magma was 6–7 wt%. The rear-arc Sannome-gata magma was generated by a lower degree of melting of the mantle at greater depths and lower temperatures than the frontal-arc magma from the Iwate volcano, which was also estimated to be generated by ~15 % melting of the source mantle with 0.6–0.7 wt% H₂O at ~1,250 °C and at ~1.3 GPa.     

Lavoisierite, Mn2+ 8[Al10(Mn3+Mg)][Si11P]O44(OH)12, a new mineral from Piedmont, Italy: the link between “ardennite” and sursassite

The new mineral species lavoisierite, ideally Mn²⁺ ₈[Al₁₀(Mn³⁺Mg)][Si₁₁P]O₄₄(OH)₁₂, has been discovered in piemontite-bearing micaschists belonging to the Piedmontese Nappe from Punta Gensane, Viù Valley, Western Alps, Italy. It occurs as yellow-orange acicular to prismatic-tabular crystals up to a few millimeters in length, with white streak and vitreous luster, elongated along [010] and flattened on {001}. Lavoisierite is associated with quartz, “mica,” sursassite, piemontite, spessartine, braunite, and “tourmaline.” Calculated density is 3.576 g cm^?3. In plane-polarized light, it is transparent, pleochroic, with pale yellow parallel to [010] and yellow-orange normal to this direction; extinction is parallel and elongation is positive. Birefringence is moderate; the calculated average refraction index n is 1.750. Lavoisierite is orthorhombic, space group Pnmm, with a 8.6891(10), b 5.7755(3), c 36.9504(20) Å, V 1854.3(2) Å³, Z = 2. Calculated main diffraction lines of the X-ray powder diffraction pattern are [d in Å, (I), (hkl); relative intensities are visually estimated]: 4.62 (m) (112), 2.931 (vs) (1110), 2.765 (s) (1111), 2.598 (s) (310), 2.448 (ms) (028). Chemical analyses by electron microprobe give (in wt%) P₂O₅ 2.08, V₂O₅ 0.37, SiO₂ 34.81, TiO₂ 0.13, Al₂O₃ 22.92, Cr₂O₃ 0.32, Fe₂O₃ 0.86, Mn₂O₃ 6.92, MnO 19.09, MgO 5.73, CaO 1.94, Na₂O 0.01, H₂O 5.44, sum 100.62 wt%. H₂O content was calculated from structure refinement. The empirical formula, based on 56 anions, is (Mn _5.340 ²⁺ Mg_1.810Ca_0.686Na_0.006)_Σ=7.852(Al_8.921Mn _1.739 ³⁺ Mg_1.010Fe _0.214 ³⁺ Cr_0.084Ti_0.032)_Σ=12.000(Si_11.496P_0.582V_0.081)_Σ=12.159O_43.995(OH)_12.005. The crystal structure of lavoisierite was solved by direct methods and refined on the basis of 1743 observed reflections to R ₁ = 4.6 %. The structure is characterized by columns of edge-sharing octahedra running along [010] and linked to each other by means of [SiO₄], [Si₂O₇], and [Si₃O₁₀] groups. Lavoisierite, named after the French chemist and biologist Antoine-Laurent de Lavoisier (1743–1794), displays an unprecedented kind of structure, related to those of “ardennite” and sursassite.     

Cold subduction of the Neotethys: the metamorphic record from finely banded lawsonite and epidote blueschists and associated metabasalts of the Nagaland Ophiolite Complex,India

In this study, we have deduced the thermal history of the subducting Neotethys from its eastern margin, using a suite of partially hydrated metabasalts from a segment of the Nagaland Ophiolite Complex (NOC), India. Located along the eastern extension of the Indus‐Tsangpo suture zone (ITSZ), the N–S‐trending NOC lies between the Indian and Burmese plates. The metabasalts, encased within a serpentinitic mélange, preserve a tectonically disturbed metamorphic sequence, which from west to east is greenschist (GS), pumpellyite–diopside (PD) and blueschist (BS) facies. Metabasalts in all the three metamorphic facies record prograde metamorphic overprints directly on primary igneous textures and igneous augite. In the BS facies unit, the metabasalts interbedded with marble show centimetre‐ to metre‐scale interlayering of lawsonite blueschist (LBS) and epidote blueschist (EBS). Prograde HP/LT metamorphism stabilized lawsonite + omphacite (X_Jd = 0.50–0.56 to 0.26–0.37) + jadeite (X_Jd = 0.67–0.79) + augite + ferroglaucophane + high‐Si phengite (Si = 3.6–3.65 atoms per formula unit, a.p.f.u.) + chlorite + titanite + quartz in LBS and lawsonite + glaucophane/ferroglaucophane ± epidote ± omphacite (X_Jd = 0.34) + chlorite + phengite (Si = 3.5 a.p.f.u.) + titanite + quartz in EBS at the metamorphic peak. Retrograde alteration, which was pervasive in the EBS, produced a sequence of mineral assemblages from omphacite and lawsonite‐absent, epidote + glaucophane/ferroglaucophane + chlorite + phengite + titanite + quartz through albite + chlorite + glaucophane to lawsonite + albite + high‐Si phengite (Si = 3.6–3.7 a.p.f.u.) + glaucophane + epidote + quartz. In the PD facies metabasalts, the peak mineral assemblage, pumpellyite + chlorite + titanite + phengitic white mica (Si = 3.4–3.5 a.p.f.u.) + diopside appeared in the basaltic groundmass from reacting titaniferous augite and low‐Si phengite, with prehnite additionally producing pumpellyite in early vein domains. In the GS facies metabasalts, incomplete hydration of augite produced albite + epidote + actinolite + chlorite + titanite + phengite + augite mineral assemblage. Based on calculated T–M(H₂O), T–M(O₂) (where M represents oxide mol.%) and P–T pseudosections, peak P–T conditions of LBS are estimated at ~11.5 kbar and ~340 °C, EBS at ~10 kbar, 325 °C and PD facies at ~6 kbar, 335 °C. Reconstructed metamorphic reaction pathways integrated with the results of P–T pseudosection modelling define a near‐complete, hairpin, clockwise P–T loop for the BS and a prograde P–T path with a steep dP/dT for the PD facies rocks. Apparent low thermal gradient of 8 °C km^?1 corresponding to a maximum burial depth of 40 km and the hairpin P–T trajectory together suggest a cold and mature stage of an intra‐oceanic subduction zone setting for the Nagaland blueschists. The metamorphic constraints established above when combined with petrological findings from the ophiolitic massifs along the whole ITSZ suggest that intra‐oceanic subduction systems within the Neotethys between India and the Lhasa terrane/the Karakoram microcontinent were also active towards east between Indian and Burmese plates.     

Constraining peak P–T conditions in UHP eclogites: calculated phase equilibria in kyanite‐ and phengite‐bearing eclogite of the Tromsø Nappe,Norway

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 (X_Grs = 0.25–0.29), but lower pyrope‐content (X_Prp = 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 (X_Ca^Grt = 0.18–0.21) and symplectite clinopyroxene (X_Na^Cpx = 0.13–0.21), and to 0.5–0.7 GPa at 700–800 °C by sapphirine (X_Mg = 0.86–0.87) and spinel (X_Mg = 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.     

Cu- and Mn-bearing tourmalines from Brazil and Mozambique: crystal structures, chemistry and correlations

Cu- and Mn-bearing tourmalines from Brazil and Mozambique were characterised chemically (EMPA and LA-ICP-MS) and by X-ray single-crystal structure refinement. All these samples are rich in Al, Li and F (fluor-elbaite) and contain significant amounts of CuO (up to ~1.8 wt%) and MnO (up to ~3.5 wt%). Structurally investigated samples show a pronounced positive correlation between the <Y-O> distances and the (Li + Mn²⁺ + Cu + Fe²⁺) content (apfu) at this site with R ² = 0.90. An excellent negative correlation exists between the <Y-O> distances and the Al₂O₃ content (R ² = 0.94). The samples at each locality generally show a strong negative correlation between the X-site vacancies and the (MnO + FeO) content. The Mn content in these tourmalines depends on the availability of Mn, on the formation temperature, as well as on stereochemical constraints. Because of a very weak correlation between MnO and CuO we believe that the Cu content in tourmaline is essentially dependent on the availability of Cu and on stereochemical constraints.     

Mineralogy, conditions of crystallization and melt generation of epidote-bearing porphyries from the Middle Urals, Russian federation

Epidote-bearing porphyritic dikes (whole rock analysis: SiO₂?=?55–65 wt. %, MgO <2.1 wt. %, K₂O <2.5 wt. %, Al₂O₃ >17 wt. %, Na₂O + K₂O?=?5.7–9.4 wt. %) situated in the continental margin zone, the Middle Urals, Russian Federation have been dated using SHRIMP U-Pb zircon techniques and give a Middle Devonian age of 388?±?2 Ma and 389?±?6 Ma. The porphyries contain phenocrysts of magmatic epidote (Ps?=?17–25 %), Ca- and Mn-rich (CaO >9 wt. %; MnO >6 wt. %) almandine garnet, Al-rich (Al₂O₃?=?12–16 wt. %) amphibole, titanite, plagioclase, biotite, muscovite, apatite, and quartz. 60 to 70 % groundmass of the porphyritic dikes consists of fine-grained albite, quartz, and K-feldspar. A variety of thermobarometric estimations, plus comparison with published experimental data indicate that the phenocryst assemblage was stable between 5 and 11 kbar and 690 to 800 °C. Oxygen fugacity was close to or greater than logfo₂ = Ni-NiO + 1. Later stage formation of the quartz-feldspar groundmass took place at hypabyssal conditions, corresponding to 1 to 2 kbar and 660 to 690 °C. The porphyritic dikes are metaluminous to slightly peraluminous (ACNK?=?0.7–1.17). They are enriched in REE and depleted Nb and Ti. They show features typical of subduction-related magmas. Chemical composition and isotopic ratios of ⁸⁶Sr/⁸⁷Sr_i?=?0.709–0.720 suggest that both mantle- and deep crustal-derived materials were involved in their petrogenesis.     

Jadeite–chloritoid–glaucophane–lawsonite blueschists in north-west Turkey: unusually high P/T ratios in continental crust

Sodic metapelites with jadeite, chloritoid, glaucophane and lawsonite form a coherent regional metamorphic sequence, several tens of square kilometres in size, and over a kilometre thick, in the Orhaneli region of northwest Turkey. The low‐variance mineral assemblage in the sodic metapelites is quartz + phengite + jadeite + glaucophane + chloritoid + lawsonite. The associated metabasites are characterized by sodic amphibole + lawsonite ± garnet paragenesis. The stable coexistence of jadeite + chloritoid + glaucophane + lawsonite, not reported before, indicates metamorphic pressures of 24 ± 3 kbar and temperatures of 430 ± 30 °C for the peak blueschist facies conditions. These P–T conditions correspond to a geotherm of 5 °C km^?1, one of the lowest recorded in continental crustal rocks. The low geotherm, and the known rate of convergence during the Cretaceous subduction suggest low shear stresses at the top of the downgoing continental slab.     

Petrology of the Strathgordon area,Western Tasmania: Si4+‐content of phengite mica as monitor of metamorphic grade

Important mineral assemblages of metapelite and quartzite of the Strathgordon area are phengite + chlorite + tourmaline + quartz and phengite + garnet + chlorite + tourmaline + quartz. Over a limited area the Si⁴⁺‐content of phengite does not vary significantly and is considered to depend only on the PT regime. The Si⁴⁺‐content of phengite coexisting with almandine‐grossular‐spessartine garnet and tourmaline indicate that the maximum metamorphism of the area occurred at 400 ± 50°C and 3 ± 1 kb.     

Rapid pre-eruptive thermal rejuvenation in a large silicic magma body: the case of the Masonic Park Tuff,Southern Rocky Mountain volcanic field,CO, USA

Determining the mechanisms involved in generating large-volume eruptions (>100 km³) of silicic magma with crystallinities approaching rheological lock-up (~50 vol% crystals) remains a challenge for volcanologists. The Cenozoic Southern Rocky Mountain volcanic field, in Colorado and northernmost New Mexico, USA, produced ten such crystal-rich ignimbrites within 3 m.y. This work focuses on the 28.7 Ma Masonic Park Tuff, a dacitic (~62–65 wt% SiO₂) ignimbrite with an estimated erupted volume of ~500 km³ and an average of ~45 vol% crystals. Near-absence of quartz, titanite, and sanidine, pronounced An-rich spikes near the rims of plagioclase, and reverse zoning in clinopyroxene record the reheating (from ~750 to >800?°C) of an upper crustal mush in response to hotter recharge from below. Zircon U–Pb ages suggest prolonged magmatic residence, while Yb/Dy vs temperature trends indicate co-crystallization with titanite which was later resorbed. High Sr, Ba, and Ti concentrations in plagioclase microlites and phenocryst rims require in-situ feldspar melting and concurrent, but limited, mass addition provided by the recharge, likely in the form of a melt-gas mixture. The larger Fish Canyon Tuff, which erupted from the same location ~0.7 m.y. later, also underwent pre-eruptive reheating and partial melting of quartz, titanite, and feldspars in a long-lived upper crustal mush following the underplating of hotter magma. The Fish Canyon Tuff, however, records cooler pre-eruptive temperatures (~710–760?°C) and a mineral assemblage indicative of higher magmatic water contents (abundant resorbed sanidine and quartz, euhedral amphibole and titanite, and absence of pyroxene). These similar pre-eruptive mush-reactivation histories, despite differing mineral assemblages and pre-eruptive temperatures, indicate that thermal rejuvenation is a key step in the eruption of crystal-rich silicic volcanics over a wide range of conditions.