Aragonite and magnesite in eclogites from the Jæren nappe,SW Norway: disequilibrium in the system CaCO3–MgCO3 and petrological implications

Eclogites from the Jæren nappe in the Caledonian orogenic belt of SW Norway contain aragonite, magnesite and dolomite in quartz‐rich layers. The carbonates comprise composite grains that occur interstitially between phases of the eclogite facies assemblage: garnet + omphacite + zoisite + clinozoisite + quartz + apatite + rutile ± dolomite ± kyanite ± phengite. Pressure and temperature conditions for the main eclogite stage are estimated to be 2.3–2.8 GPa and 585–655 °C. Published ultrahigh pressure (UHP) experiments on CaO‐, MgO‐ and CO₂‐bearing systems have shown that equilibrium assemblages of aragonite and magnesite form as a result of dolomite breakdown at pressures >5 GPa. As a result, recognition of magnesite and aragonite in eclogite facies rocks has been used as an indicator for UHP conditions. However, petrological testing showed that the samples studied here have not experienced such conditions. Aragonite and magnesite show disequilibrium textures that indicate replacement of magnesite by aragonite. This process is inferred to have occurred via a coupled dissolution–precipitation reaction. The formation of aragonite is constrained to eclogite facies conditions, which implies that the studied rocks have experienced metasomatic, reactive fluid flow during their residence at high pressure (HP) conditions. During decompression, the bimineralic carbonate aggregates were overgrown by rims of dolomite, which partially reacted with aragonite to form Mg‐calcite. The well‐preserved carbonate assemblages and textures observed in the studied samples provide a detailed record of the reaction series that affected the rocks during and after their residence at P–T conditions near the coesite stability field. Recognition of the HP mechanism of magnesite replacement by aragonite provides new insight into metasomatic processes that occur in subduction zones and illustrates how fluids facilitate HP carbonate reactions that do not occur in dry systems at otherwise identical physiochemical conditions. This study documents that caution is warranted in interpreting aragonite‐magnesite associations in eclogite facies rocks as evidence for UHP metamorphic conditions.     

大别山北部超高压变质大理岩及其地质意义

岩石学研究表明 ,大别山北部镁铁 超镁铁质岩带中白云质大理岩至少经历过三期变质阶段 :(1)榴辉岩相峰期变质阶段 ,矿物组合主要为方解石 +白云石 +金红石 +镁橄榄石 +钛 斜硅镁石 +富镁的钛铁矿±文石±石榴子石 ;(2 )麻粒岩相退变质阶段 ,矿物组合主要为方解石 +白云石 +金云母 +镁橄榄石 +透辉石 +钛铁矿 +尖晶石±斜方辉石等 ;(3)角闪岩相退变质阶段 ,主要矿物组合为方解石 +白云石 +磷灰石 +磁铁矿+榍石等。它的峰期变质矿物组合 ,类似于苏 鲁超高压大理岩 ,形成压力至少大于 2 .5GPa。这进一步证明 ,大别山北部大多数高级变质岩 (包括大理岩等 )都曾经过超高压变质作用 ,应属于印支期扬子俯冲陆壳的一部分。     

Omphacite-bearing calcite marble and associated coesite-bearing pelitic schist from the meta-ophiolitic belt of Chinese western Tianshan

In the meta-ophiolitic belt of Chinese western Tianshan, marble (5–50 cm thick) is found interlayered with pelitic schist. The marble is mainly composed of calcite (>90% in volume) and accessory phases include omphacite, quartz, dolomite, albite, phengite, clinozoisite and titanite with or without rutile core. This is the first omphacite (Jd_35–50) reported from marble of Chinese western Tianshan. It mainly occurs in the calcite matrix, rarely as inclusion in albite. The presence of omphacite suggests that the layered marble was subjected to eclogite-facies metamorphism, consistent with the occurrence of high-Si phengite (Si a.p.f.u. up to 3.7) and aragonite relic in albite. The associated pelitic schist consists of quartz, white mica (phengite + paragonite), garnet, albite, amphibole (barroisite ± glaucophane) and rutile/titanite, as well as minor amounts of dolomite, tourmaline and graphite. Coesite is optically recognized within porphyroblastic pelitic garnet and is further confirmed via Raman spectroscopy. Thermodynamic models support the UHP metamorphism of calcite marble, similar to the associated pelitic schist. Shared UHP-LT history of calcareous and pelitic rocks in Chinese western Tianshan suggests that the supracrustal carbon-rich sediments have been carried to depths of >90 km during fast subduction and thus are potential sources for carbon recycled into arc crust.     

The Habutengsu metapelites and metagreywackes in western Tianshan,China: metamorphic evolution and tectonic implications

The HP‐UHP metamorphic belt of western Tianshan in northwestern China is a rarely preserved oceanic UHP terrane which consists predominantly of meta‐siliciclastic rocks, occasionally accompanied by lens‐shaped metabasites. The metapelites and metagreywackes from the Habutengsu Valley and adjacent area within this belt contain quartz, albite, garnet, white mica, chlorite and rutile/titanite, with or without minor amounts of barroisite, glaucophane, clinozoisite, allanite, graphite, carbonate and tourmaline. Included in coarse‐grained garnet, pseudomorphs of clinozoisite + paragonite after lawsonite are common, seldom also together with inclusions of chloritoid, jadeite and glaucophane. In the northern Habutengsu area, garnet is compositionally characterized by similar cores with consistently low‐Ca content. Similar garnet armouring coesite has been reported in UHP schists from the same area. Deduced P–T conditions during formation of these Ca‐poor garnet cores are 25–31 kbar and 430–510 °C, which are consistent with the computed stability of the observed assemblage Grt + Gln + Lws ± Jd ± Cld in the coesite stability field. Thus, the occurrences of the UHP metapelites and metagreywackes define an internally coherent UHP unit in the north of the Habutengsu area, the spatial extension of which is much larger than previously known. Compared with the northern ones, the southern metapelites and metagreywackes in the Habutengsu area consist of similar minerals and have similar bulk rock compositions but significantly different garnet chemistry, indicating an abrupt variation in P–T conditions during garnet growth. The derived conditions initiating the garnet growth for the southern rocks in a similar range (18–21 kbar and 450–500 °C) and thus constrain a coherent HP unit in the south of the Habutengsu area. The juxtaposition of two exhumed slices of contrasting metamorphic grades probably indicates the change of subduction dynamics of the palaeo‐Tianshan oceanic crust, the subduction polarity (from south to north) of which accounts for the spatial relationship between these two units.     

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.     

Redox evolution of western Tianshan subduction zone and its effect on deep carbon cycle

Knowing the phase relations of carbon-bearing phases at high-pressure(HP) and high-temperature(HT) condition is essential for understanding the deep carbon cycle in the subduction zones.In particular,the phase relation of carbon-bearing phases is also strongly influenced by redox condition of subduction zones,which is poorly explored.Here we summarized the phase relations of carbon-bearing phases(calcite,aragonite,dolomite,magnesite,graphite,hydrocarbon) in HP metamorphic rocks(marble,metapelite,eclogite) from the Western Tianshan subduction zone and high-pressure experiments.During prograde progress of subduction,carbonates in altered oceanic crust change from Ca-carbonate(calcite) to Ca,Mg-carbonate(dolomite),then finally to Mgcarbonate(magnesite) via Mg-Ca cation exchange reaction between silicate and carbonate,while calcite in sedimentary calcareous ooze on oceanic crust directly transfers to high-pressure aragonite in marble or amorphous CaCO3 in subduction zones.Redox evolution also plays a significant effect on the carbon speciation in the Western Tianshan subduction zone.The prograde oxygen fugacity of the Western Tianshan subduction zone was constrained by mineral assemblage of garnet-omphacite from FMQ-1.9 to FMQ-2.5 at its metamorphic peak(maximum P-T) conditions.In comparison with redox conditions of other subduction zones,Western Tianshan has the lowest oxygen fugacity.Graphite and light hydrocarbon inclusions were ubiqutously identified in Western Tianshan HP metamorphic rocks and speculated to be formed from reduction of Fe-carbonate at low redox condition,which is also confirmed by high-pressure experimental simulation.Based on petrological observation and high-pressure simulation,a polarized redox model of reducing slab but oxidizing mantle wedge in subduction zone is proposed,and its effect on deep carbon cycle in subduction zones is further discussed.     

Fate of carbonates within oceanic plates subducted to the lower mantle, and a possible mechanism of diamond formation

We report on high-pressure and high-temperature experiments involving carbonates and silicates at 30–80 GPa and 1,600–3,200 K, corresponding to depths within the Earth of approximately 800–2,200 km. The experiments are intended to represent the decomposition process of carbonates contained within oceanic plates subducted into the lower mantle. In basaltic composition, CaCO₃ (calcite and aragonite), the major carbonate phase in marine sediments, is altered into MgCO₃ (magnesite) via reactions with Mg-bearing silicates under conditions that are 200–300°C colder than the mantle geotherm. With increasing temperature and pressure, the magnesite decomposes into an assemblage of CO₂ + perovskite via reactions with SiO₂. Magnesite is not the only host phase for subducted carbon—solid CO₂ also carries carbon in the lower mantle. Furthermore, CO₂ itself breaks down to diamond and oxygen under geotherm conditions over 70 GPa, which might imply a possible mechanism for diamond formation in the lower mantle.     

SHRIMP U-Pb zircon dating from Sulu-Dabie dolomitic marble, eastern China: constraints on prograde, ultrahigh-pressure and retrograde metamorphic ages

Laser Raman spectroscopy and cathodoluminescence (CL) images show that zircon from Sulu‐Dabie dolomitic marbles is characterized by distinctive domains of inherited (detrital), prograde, ultrahigh‐pressure (UHP) and retrograde metamorphic growths. The inherited zircon domains are dark‐luminescent in CL images and contain mineral inclusions of Qtz + Cal + Ap. The prograde metamorphic domains are white‐luminescent in CL images and preserve a quartz eclogite facies assemblage of Qtz + Dol + Grt + Omp + Phe + Ap, formed at 542–693 °C and 1.8–2.1 GPa. In contrast, the UHP metamorphic domains are grey‐luminescent in CL images, retain the UHP assemblage of Coe + Grt + Omp + Arg + Mgs + Ap, and record UHP conditions of 739–866 °C and >5.5 GPa. The outermost retrograde rims have dark‐luminescent CL images, and contain low‐P minerals such as calcite, related to the regional amphibolite facies retrogression. Laser ablation ICP‐MS trace‐element data show striking difference between the inherited cores of mostly magmatic origin and zircon domains grown in response to prograde, UHP and retrograde metamorphism. SHRIMP U‐Pb dating on these zoned zircon identified four discrete ²⁰⁶Pb/²³⁸U age groups: 1823–503 Ma is recorded in the inherited (detrital) zircon derived from various Proterozoic protoliths, the prograde domains record the quartz eclogite facies metamorphism at 254–239 Ma, the UHP growth domains occurred at 238–230 Ma, and the late amphibolite facies retrogressive overprint in the outermost rims was restricted to 218–206 Ma. Thus, Proterozoic continental materials of the Yangtze craton were subducted to 55–60 km depth during the Early Triassic and recrystallized at quartz eclogite facies conditions. Then these metamorphic rocks were further subducted to depths of 165–175 km in the Middle Triassic and experienced UHP metamorphism, and finally these UHP metamorphic rocks were exhumed to mid‐crustal levels (about 30 km) in the Late Triassic and overprinted by regional amphibolite facies metamorphism. The subduction and exhumation rates deduced from the SHRIMP data and metamorphic P–T conditions are 9–10 km Myr^?1 and 6.4 km Myr^?1, respectively, and these rapid subduction–exhumation rates may explain the obtained P–T–t path. Such a fast exhumation suggests that Sulu‐Dabie UHP rocks that returned towards crustal depths were driven by buoyant forces, caused as a consequence of slab breakoff at mantle depth.     

Subduction metamorphism of serpentinite‐hosted carbonates beyond antigorite‐serpentinite dehydration (Nevado‐Filábride Complex,Spain)

At sub‐arc depths, the release of carbon from subducting slab lithologies is mostly controlled by fluid released by devolatilization reactions such as dehydration of antigorite (Atg‐) serpentinite to prograde peridotite. Here we investigate carbonate–silicate rocks hosted in Atg‐serpentinite and prograde chlorite (Chl‐) harzburgite in the Milagrosa and Almirez ultramafic massifs of the palaeo‐subducted Nevado‐Filábride Complex (NFC, Betic Cordillera, S. Spain). These massifs provide a unique opportunity to study the stability of carbonate during subduction metamorphism at P–T conditions before and after the dehydration of Atg‐serpentinite in a warm subduction setting. In the Milagrosa massif, carbonate–silicate rocks occur as lenses of Ti‐clinohumite–diopside–calcite marbles, diopside–dolomite marbles and antigorite–diopside–dolomite rocks hosted in clinopyroxene‐bearing Atg‐serpentinite. In Almirez, carbonate–silicate rocks are hosted in Chl‐harzburgite and show a high‐grade assemblage composed of olivine, Ti‐clinohumite, diopside, chlorite, dolomite, calcite, Cr‐bearing magnetite, pentlandite and rare aragonite inclusions. These NFC carbonate–silicate rocks have variable CaO and CO₂ contents at nearly constant Mg/Si ratio and high Ni and Cr contents, indicating that their protoliths were variable mixtures of serpentine and Ca‐carbonate (i.e., ophicarbonates). Thermodynamic modelling shows that the carbonate–silicate rocks attained peak metamorphic conditions similar to those of their host serpentinite (Milagrosa massif; 550–600°C and 1.0–1.4 GPa) and Chl‐harzburgite (Almirez massif; 1.7–1.9 GPa and 680°C). Microstructures, mineral chemistry and phase relations indicate that the hybrid carbonate–silicate bulk rock compositions formed before prograde metamorphism, likely during seawater hydrothermal alteration, and subsequently underwent subduction metamorphism. In the CaO–MgO–SiO₂ ternary, these processes resulted in a compositional variability of NFC serpentinite‐hosted carbonate–silicate rocks along the serpentine‐calcite mixing trend, similar to that observed in serpentinite‐hosted carbonate‐rocks in other palaeo‐subducted metamorphic terranes. Thermodynamic modelling using classical models of binary H₂O–CO₂ fluids shows that the compositional variability along this binary determines the temperature of the main devolatilization reactions, the fluid composition and the mineral assemblages of reaction products during prograde subduction metamorphism. Thermodynamic modelling considering electrolytic fluids reveals that H₂O and molecular CO₂ are the main fluid species and charged carbon‐bearing species occur only in minor amounts in equilibrium with carbonate–silicate rocks in warm subduction settings. Consequently, accounting for electrolytic fluids at these conditions slightly increases the solubility of carbon in the fluids compared with predictions by classical binary H₂O–CO₂ fluids, but does not affect the topology of phase relations in serpentinite‐hosted carbonate‐rocks. Phase relations, mineral composition and assemblages of Milagrosa and Almirez (meta)‐serpentinite‐hosted carbonate–silicate rocks are consistent with local equilibrium between an infiltrating fluid and the bulk rock composition and indicate a limited role of infiltration‐driven decarbonation. Our study shows natural evidence for the preservation of carbonates in serpentinite‐hosted carbonate–silicate rocks beyond the Atg‐serpentinite breakdown at sub‐arc depths, demonstrating that carbon can be recycled into the deep mantle.     

Petrology of coesite-bearing eclogite from Habutengsu Valley, western Tianshan, NW China and its tectonometamorphic implication

Coesite inclusions in garnet have been found in eclogite boudins enclosed in coesite‐bearing garnet micaschist in the Habutengsu Valley, Chinese western Tianshan, which are distinguished from their retrograde quartz by means of optical characteristics, CL imaging and Raman spectrum. The coesite‐bearing eclogite is mainly composed of porphyroblastic garnet, omphacite, paragonite, glaucophane and barroisite, minor amounts of rutile and dotted (or banded) graphite. In addition to coesite and quartz, the zoned porphyroblastic garnet contains inclusions of omphacite, Na‐Ca amphibole, calcite, albite, chlorite, rutile, ilmenite and graphite. Multi‐phase inclusions (e.g. Czo + Pg ± Qtz, Grt II + Qtz and Chl + Pg) can be interpreted as breakdown products of former lawsonite and possibly chloritoid. Coesite occurs scattered within a compositionally homogenous but narrow domain of garnet (outer core), indicative of equilibrium at the UHP stage. The estimate by garnet‐clinopyroxene thermometry yields peak temperatures of 420–520 °C at 2.7 GPa. Phase equilibrium calculations further constrain the P–T conditions for the UHP mineral assemblage Grt + Omp + Lws + Gln + Coe to 2.4–2.7 GPa and 470–510 °C. Modelled modal abundances of major minerals along a 5 °C km^?1 geothermal gradient suggests two critical dehydration processes at ～430 and ～510 °C respectively. Computed garnet composition patterns are in good agreement with measured core‐rim profiles. The petrological study of coesite‐bearing eclogite in this paper provides insight into the metamorphic evolution in a cold subduction zone. Together with other reported localities of UHP rocks from the entire orogen of Chinese western Tianshan, it is concluded that the regional extent of UHP‐LT metamorphism in Chinese western Tianshan is extensive and considerably larger than previously thought, although intensive retrogression has erased UHP‐LT assemblages at most localities.     

Aragonite in California Glaucophane Schists, and the Kinetics of the Aragonite--Calcite Transformation

Coleman & Lee's discovery that aragonite is a widespreadmetamorphic mineral in California glaucophane schists is confirmedand amplified. Methods of microscopic distinction between aragonite,calcite, and dolomite, including a universal-stage technique,are described. Further data are recorded regarding the paragenesisof aragonite-bearing glaucophane and lawsonite schists. Carbonatesin the greenschist facies are found to be exclusively calciteand dolomite. In many Californian metamorphic aragonites partialinversion to calcite has been observed. This appears to be anequal-volume replacement in which an a axis and an edge [f:f] of calcite—both directions of Closest spacing of Ca⁺⁺ions—commonlyare parallel to of the crystal axes a, b, and c of aragonite. The problem of survival of metamorphic aragonite through a necessarilylong period of post-metamorphic unloading is approached by experimentalexploration of the kinetics of the aragonite calcite transformation.It is found that Californian aragonite could survive unloadingfrom a depth of 20 km if the linear temperature gradient were10? C per km, but not appreciably higher. Available experimentaldata are consistent with crystallization of aragonite, jadeite,and lawsonite at depths of 20–30 km if a gradient of 10?C per km is assumed. The corresponding conditions of the glaucophane-schistfacies (T = 2OO?-3OO? C, P = 6000-9000 bars) are attributedessentially to deep burial in regions (subsiding geosyn-clines)of unusually low temperature gradient (10? C per km).     

Ultra-high-pressure metamorphism of carbonate rocks in the Dabie Mountains, central China

Abstract Widespread ultra-high-P assemblages including coesite, quartz pseudomorphs after coesite, aragonite, and calcite pseudomorphs after aragonite in marble, gneiss and phengite schist are present in the Dabie Mountains eclogite terrane. These assemblages indicate that the ultra-high-P metamorphic event occurred on a regional scale during Triassic collision between the Sino-Korean and Yangtze cratons. Marble in the Dabie Mountains is interlayered with coesite-bearing eclogite and gneiss and as blocks of various size within gneiss. Discontinuous boudins of eclogite occur within marble layers. Marble contains an ultra-high-P assemblage of calcite/aragonite, dolomite, clinopyroxene, garnet, phengite, epidote, rutile and quartz/coesite. Coesite, quartz pseudomorphs after coesite, aragonite and calcite pseudomorphs after aragonite occur as fine-grained inclusions in garnet and omphacite. Phengites contain about 3.6 Si atoms per formula unit (based on 11 oxygens). Similar to the coesite-bearing eclogite, marble exhibits retrograde recrystallization under amphibolite–greenschist facies conditions generated during uplift of the ultra-high-P metamorphic terrane. Retrograde minerals are fine grained and replace coarse-grained peak metamorphic phases. The most typical replacements are: symplectic pargasitic hornblende + epidote after garnet, diopside + plagioclase (An₁₈) after omphacite, and fibrous phlogopite after phengite. Ferroan pargasite + plagioclase, and actinolite formed along grain boundaries between garnet and calcite, and calcite and quartz, respectively. The estimated peak P–T conditions for marble are comparable to those for eclogite: garnet–clinopyroxene geothermometry yields temperatures of 630–760°C; the garnet–phengite thermometer gives somewhat lower temperatures. The minimum pressure of peak metamorphism is 27 kbar based on the occurrence of coesite. Such estimates of ultra-high-P conditions are consistent with the coexistence of grossular-rich garnet + rutile, and the high jadeite content of omphacite in marble. The fluid for the peak metamorphism was calculated to have a very low X_CO2 (<0.03). The P–T conditions for retrograde metamorphism were estimated to be 475–550°C at <7 kbar.     

Origin and diagenetic evolution of Ca–Mg–Fe carbonates in some coalfields of Japan

Carbonate concretions, lenses and bands in the Pleistocene, Palaeogene and Upper Triassic coalfields of Japan consist of various carbonate minerals with varied chemical compositions. Authigenic carbonates in freshwater sediments are siderite > calcite > ankerite > dolomite >> ferroan magnesite; in brackish water to marine sediments in the coal measures, calcite > dolomite > ankerite > siderite >> ferroan magnesite; and in the overlying marine deposits, calcite > dolomite >> siderite. Most carbonates were formed progressively during burial within a range of depths between the sediment-water interface and approximately 3 km. The mineral species and the chemical composition of the carbonates are controlled primarily by the initial sedimentary facies of the host sediments and secondarily by the diagenetic evolution of pore water during burial. Based on the regular sequence and burial depth of precipitation of authigenic carbonates in a specific sedimentary facies, three diagenetic stages of carbonates are proposed. Carbonates formed during Stage I (< 500 m) strongly reflect the initial sedimentary facies, e.g. low Ca-Mg siderite in freshwater sediments which are initially rich in iron derived from lateritic soil on the nearby landmass, and Mg calcite and dolomite in brackish-marine sediments whose pore waters abound in Ca²⁺ and Mg²⁺ originating in seawater and calcareous shells. Carbonates formed during Stage II (500–2000 m) include high Ca-Mg siderite, ankerite, Fe dolomite and Fe–Mg calcite in freshwater sediments. The assemblage of Stage II carbonates in brackish-marine sediments in the coal measures is similar to that in freshwater sediments. This suggests similar diagenetic environments owing to an effective migration and mixing of pore water due to the compaction of host sediments. Carbonates formed during Stage III (> 2000 m) are Fe calcite and extremely high Ca-Mg siderite; the latter is exclusively in marine mudstones. The supply of Ca is partly from the alteration of silicates in the sediments at elevated burial temperatures. After uplift, calcite with low Mg content precipitates from percolating groundwater and fills extensional cracks.     

蚀变洋壳玄武岩俯冲过程中含碳矿物相变质演化及脱碳作用的研究

俯冲作用是连接地表系统和地球深部系统的最为关键的地质过程,其对研究地球深部碳循环具有重要的意义。俯冲洋壳岩石圈中的碳主要存储在沉积物、蚀变洋壳玄武岩以及蛇纹岩中。俯冲变质作用过程含碳岩石的变质演化控制着其中含碳矿物相的转变及碳迁移过程。本文选取了蚀变洋壳玄武岩进行相平衡模拟,来研究其含碳矿物相的变质演化过程。计算结果表明,变质玄武岩体系中的碳酸盐矿物之间的转变反应除了受压力控制之外,还受到温度和体系中铁含量的影响。随着压力的升高蚀变玄武岩中碳酸盐矿物会发生方解石/文石-白云石-菱镁矿的转变,但在高压/超高压条件下,温度的升高可以使菱镁矿转变成白云石。碳酸盐矿物中的铁含量受到体系中铁含量的影响,白云石和菱镁矿中的铁含量随着体系中铁含量的增加而增加。在水不饱和条件下,洋壳不管是沿着低温还是高温地热梯度线俯冲到岛弧深度,蚀变玄武岩体系几乎都不发生脱碳作用。然而在水饱和条件下,当洋壳沿着高温以及哥斯达黎加地热梯度线俯冲到岛弧深度时,蚀变玄武岩体系中的碳几乎可以全部脱出去。蚀变玄武岩体系中水含量的增加可以促进体系的脱碳作用。     

Tectonic setting, petrology and geochronology of jadeite + glaucophane and chloritoid + glaucophane schists from north-west Turkey

The north-west Turkish blueschists represent a subducted passive continental margin sequence dominated by metaclastic rocks and marble. The depositional age of the blueschist protoliths are probably Palaeozoic to Mesozoic, while the age of the high-pressure/low-temperature metamorphism is Late Cretaceous. Blueschists are tectonically overlain by a volcanosedimentary sequence made up of accreted oceanic crustal material that locally shows incipient blueschist metamorphism and by spinel peridotite slices. The metaclastic rocks with regional jadeite and glaucophane, which comprise the lower part of the blueschist unit, make up an over 1000-m-thick coherent sequence in the Kocasu region of north-west Turkey. Rare metabasic horizons in the upper parts of the metaclastic sequence with sodic amphibole + Iawsonite but no garnet indicate lawsonite blueschist facies metamorphism. The blueschist metaclastics in the Kocasu region are practically free of calcium and ferric iron and closely approximate the NFMASH system in bulk composition. Two low-variance mineral assemblages (with quartz and phengite) are jadeite + glaucophane + chlorite + paragonite and chloritoid + glaucophane + paragonite. The metaclastics comprise up to several-metres-thick layers of jadeite schist with quartz, phengite and nearly 100 mol% jadeite. Phase relations in the metaclastics show that the chloritoid + glaucophane assemblage, even in Fe²⁺-rich compositions, is stable in the jadeite stability field. In the NFASH system the above assemblage without the accompanying garnet has a narrow thermal stability field. Mineral equilibria in the metaclastics involving chloritoid, glaucophane, jadeite, paragonite and chlorite indicate metamorphic P-T conditions of 20 ± 2 kbar and 430 ± 30 d? C, yielding geothermal gradients close to 5d? C km^-1, one of the lowest geotherms recorded. Blueschists in the Kocasu region, which have been buried to 70 km depth, are tectonically overlain by the volcanosedimentary sequence and by peridotite buried not deeper than 30 km. Phengites from two jadeite schists were dated by Ar/Ar laser probe; they give an age of 88.5 ± 0.5 Ma, interpreted as the age of metamorphism. Blueschists and the overlying peridotite bodies are intruded by 48-53-Ma-old granodiorite bodies that were emplaced at 10 km depth. This suggests that the exhumation of blueschists by underplating of cold continental crust, and normal faulting at the blueschist-peridotite, interface occurred during the Late Cretaceous to Palaeocene (88-53 Ma).     

Exsolution of dolomite and application of calcite–dolomite solvus geothermometry in high‐grade marbles: an example from Skallevikshalsen,East Antarctica

Calcite–dolomite solvus geothermometry is a versatile method for the estimation of metamorphic temperature because of its simplicity. However, in medium‐ to high‐grade metamorphic rocks the accuracy of estimating temperature by the integration of unmixed dolomite and calcite is hampered by the heterogeneous distribution of unmixed dolomite, difficulties in distinguishing between preexisting and exsolved dolomite and demarcating grain boundaries. In this study, it is shown that calcite–dolomite solvus thermometry can be applied to calcite inclusions in forsterite and spinel for the estimation of peak metamorphic temperature in granulite facies marbles from Skallevikshalsen, East Antarctica. The marbles are comprised of a granoblastic mineral assemblage of calcite + dolomite + forsterite + diopside + spinel + phlogopite ± apatite, characteristic of granulite facies metamorphic conditions. Forsterite, spinel and apatite frequently contain ‘negative crystal’ inclusions of carbonates that display homogeneously distributed dolomite lamellae. On the basis of narrow ranges of temperature (850–870 °C) recorded from carbonate inclusions compared with the range from matrix carbonate it is regarded that the inclusion carbonates represent a closed system. Furthermore, this estimate is consistent with dolomite–graphite carbon isotope geothermometry, and is considered to be the best estimate of peak metamorphic temperature for this region. Matrix calcite records different stages of retrograde metamorphism and re‐equilibration of calcite that continued until Mg diffusion ceased at ～460 °C. Electron backscattered diffraction (EBSD) results together with morphological features of unmixed coarse tabular dolomite suggest anisotropic diffusion and mineral growth are influenced by crystallographic orientation. Identification of sub‐grain boundaries and formation of fine‐grained unmixing in calcite rims suggest the presence of grain boundary fluids in the late retrograde stages of metamorphic evolution. These results, thus, demonstrate the usefulness of carbonate inclusion geothermometry in estimating the peak metamorphic temperatures of high‐grade terranes and the application of EBSD in understanding the unmixing behaviour of minerals with solid solutions.     

Ultrahigh‐pressure and high‐P lawsonite eclogites in Muzhaerte,Chinese western Tianshan

Lawsonite eclogites are crucial to decipher material recycling along a cold geotherm into the deep Earth and orogenic geodynamics at convergent margins. However, their tectono‐metamorphic role and record especially at ultrahigh‐pressure (UHP) conditions are poorly known due to rare exposure in orogenic belts. In a ~4 km long cross‐section in Muzhaerte, China, at the western termination of the HP‐UHP metamorphic belt of western Tianshan, metabasite blocks contain omphacite and lawsonite inclusions in porphyroblastic garnet, although matrix assemblages have been significantly affected by overprinting at shallower structural levels. Two types of lawsonite eclogites occur in different parts of the section and are distinguished based on inclusion assemblages in garnet: Type 1 (UHP) with the peak equilibrium assemblage garnet+omphacite±jadeite+lawsonite+rutile+coesite±chlorite±glaucophane and Type 2 (HP) with the assemblage garnet+omphacite±diopside+lawsonite+titanite+quartz±actinolite±chlorite+glaucophane. Pristine coesite and lawsonite and their pseudomorphs in Type 1 are present in the mantle domains of zoned garnet, indicative of a coesite‐lawsonite eclogite facies. Regardless of grain size and zoning profiles, garnet with Type 1 inclusions systematically shows higher Mg and lower Ca contents than Type 2 (prp_4–25grs_13–24 and prp_1–8grs_20–45 respectively). Phase equilibria modelling indicates that the low‐Ca garnet core and mantle of Type 1 formed at UHP conditions and that there was a major difference in peak pressures (i.e., maximum return depth) between the two types (2.8–3.2 GPa at 480–590°C and 1.3–1.85 GPa at 390–500°C respectively). Scattered exposures of Type 1 lawsonite eclogite is scatteredly exposed in the north of the Muzhaerte section with a structural thickness of ~1 km, whereas Type 2 occurs throughout the rest of the section. We conclude from this regular distribution that they were derived from two contrasting units that formed along two different geothermal systems (150–200°C/GPa for the northern UHP unit and 200–300°C/GPa for the southern HP unit), with subsequent stacking of UHP and HP slices at a kilometre scale.     

Chloritoid–glaucophane schist in the north Qilian orogen, NW China: phase equilibria and P–T path from garnet zonation

Chloritoid–glaucophane‐bearing rocks are widespread in the high‐pressure belt of the north Qilian orogen, NW China. They are interbedded and cofacial with felsic schists originated from greywackes, mafic garnet blueschists and low‐T eclogites. Two representative chloritoid–glaucophane‐bearing assemblages are chloritoid + glaucophane + garnet + talc + quartz (sample Q5‐49) and chloritoid + glaucophane + garnet + phengite + epidote + quartz (sample Q5‐12). Garnet in sample Q5‐49 is coarse‐, medium‐ and fine‐grained and shows two types of zonation patterns. In pattern I, X_grs is constant as X_py rises, and in pattern II X_grs decreases as X_py rises. Phase equilibrium modelling in the NC(K)MnFMASH system with Thermocalc 3.25 indicates that pattern I can be formed during progressive metamorphism in lawsonite‐stable assemblages, while pattern II zonation can be formed with further heating after lawsonite has been consumed. Garnet growth in Q5‐49 is consistent with a continuous progressive metamorphic process from ～14.5 kbar at 470 °C to ～22.5 kbar at 560 °C. Garnet in sample Q5‐12 develops with pattern I zonation, which is consistent with a progressive metamorphic process from ～21 kbar at 540 °C to ～23.5 kbar at 580 °C with lawsonite present in the whole garnet growth. The latter sample shows the highest P–T conditions of the reported chloritoid–glaucophane‐bearing assemblages. Phase equilibrium calculation in the NCKFMASH system with a recent mixing model of amphibole indicates that chloritoid + glaucophane paragenesis does not have a low‐pressure limit of 18–19 kbar as previously suggested, but has a much larger pressure range from 7–8 to 27–30 kbar, with the low‐pressure part being within the stability field of albite.     

Petrology and metamorphism of glaucophane eclogites in Changning-Menglian suture zone,Bangbing area,southeast Tibetan Plateau: An evidence for Paleo-Tethyan subduction

High/ultrahigh-pressure (HP/UHP) metamorphic complexes, such as eclogite and blueschist, are generally regarded as significant signature of paleo-subduction zones and paleo-suture zones. Glaucophane eclogites have been recently identified within the Lancang Group characterized by accretionary mélange in the Changning-Menglian suture zone, at Bangbing in the Shuangjiang area of southeastern Tibetan Plateau. The authors report the result of petrological, mineralogical and metamorphism investigations of these rocks, and discuss their tectonic implications. The eclogites are located within the Suyi blueschist belt and occur as tectonic lenses in coarse-grained garnet muscovite schists. The major mineral assemblage of the eclogites includes garnet, omphacite, glaucophane, phengite, clinozoisite and rutile. Eclogitic garnet contains numerous inclusions, such as omphacite, glaucophane, rutile, and quartz with radial cracks around. Glaucophane and clinozoisite in the matrix have apparent optical and compositional zonation. Four stages of metamorphic evolution can be determined: The prograde blueschist facies (M₁), the peak eclogite facies (M₂), the decompression blueschist facies (M₃) and retrograde greenschist facies (M₄). Using the Grt-Omp-Phn geothermobarometer, a peak eclogite facies metamorphic P-T condition of 3000–3270 MPa and 617–658°C was determined, which is typical of low-temperature ultrahigh-pressure metamorphism. The comparison of the geological characteristics of the Bangbing glaucophane eclogites and the Mengku lawsonite-bearing retrograde eclogites indicates that two suites of eclogites may have formed from significantly different depths or localities to create the tectonic mélange in a subduction channel during subduction of the Triassic Changning-Menglian Ocean. The discovery of the Bangbing glaucophane eclogites may represent a new oceanic HP/UHP metamorphic belt in the Changning-Menglian suture zone.©2021 China Geology Editorial Office.     

P–T evolution of the Precambrian Metamorphic Complex,NW Iran: a study of metapelitic rocks

The Mahneshan Metamorphic Complex (MMC) is one of the Precambrian terrains exposed in the northwest of Iran. The MMC underwent two main phases of deformation (D₁ and D₂) and at least two metamorphic events (M₁ and M₂). Critical metamorphic mineral assemblages in the metapelitic rocks testify to regional metamorphism under amphibolite‐facies conditions. The dominant metamorphic mineral assemblage in metapelitic rocks (M₁) is muscovite, biotite I, Garnet I, staurolite, Andalusite I and sillimanite. Peak metamorphism took place at 600–620°C and ∼7 kbar, corresponding to a depth of ca. 24 km. This was followed by decompression during exhumation of the crustal rocks up to the surface. The decrease of temperature and pressure during exhumation produced retrograde metamorphic assemblages (M₂). Secondary phases such as garnet II biotite II, Andalusite II constrain the temperature and pressure of M₂ retrograde metamorphism to 520–560°C and 2.5–3.5 kbar, respectively. The geothermal gradient obtained for the peak of metamorphism is 33°C km⁻¹, which indicates that peak metamorphism was of Barrovian type and occurred under medium‐pressure conditions. The MMC followed a ‘clockwise’ P–T path during metamorphism, consistent with thermal relaxation following tectonic thickening. The bulk chemistry of the MMC metapelites shows that their protoliths were deposited at an active continental margin. Together with the presence of palaeo‐suture zones and ophiolitic rocks around the high‐grade metamorphic rocks of the MMC, these features suggest that the Iranian Precambrian basement formed by an island‐arc type cratonization. Copyright © 2010 John Wiley & Sons, Ltd.