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1.
A combined powder and single-crystal X-ray diffraction analysis of dolomite [CaMg(CO3)2] heated to 1,200°C at 3 GPa was made to study the order–disorder–reorder process. The order/disorder transition is inferred to start below 1,100°C, and complete disorder is attained at approximately 1,200°C. Twinned crystals characterized by high internal order were found in samples annealed over 1,100°C, and their fraction was found to increase with temperature. Evidences of twinning domains combined with probable remaining disordered portions of the structure imply that reordering processes occur during the quench. Twin domains are hereby proposed as a witness to thermally induced intra-layer-type cation disordering.  相似文献   

2.
Melt inclusions in kimberlitic minerals and diamonds indicate that chlorides are important constituents of mantle carbonatite melts. Besides, alkaline chlorides are important constituents of saline high-density fluids (HDFs) found in diamonds from kimberlites and placers around the world. Continuous compositional variations suggest that saline and carbonatitic HDFs could be genetically linked. However, the essence of this link remains unclear owing to the lack of data on phase relations in the chloride-carbonate systems under pressure. Here we studied subsolidus and melting phase relations in the system NaCl–CaCO3–MgCO3 at 6 GPa and 1000–1600 °C using a Kawai-type multianvil press. We found that at 1000 °C, subsolidus assemblage consists of halite, magnesite, and aragonite. At higher temperatures, the stabilization of dolomite splits the subsolidus area into two partial ternary fields: halite + magnesite + dolomite and halite + dolomite + aragonite. The minimum on the liquidus surface corresponds to the halite-dolomite-aragonite ternary eutectic, situated at 1100 °C. The eutectic melt has Ca# 89 and contains 30 wt.% NaCl (26 mol% 2NaCl). The system has two ternary peritectics: halite + dolomite = magnesite + liquid located near the ternary eutectic and magnesite + dolomite = Mg-dolomite + liquid situated between 1300 and 1400 °C. Although under dry conditions incipient melting yields carbonate-dominated melt, the addition of water facilitates the fusion of NaCl and expands the liquid field to NaCl-rich compositions with up to 70 wt.% NaCl. The obtained results favor the idea that hydrous saline melts/fluids (brines) found as inclusions in diamonds could be a lower temperature derivative of mantle carbonatite melts and disagree with the hypothesis on chloride melt generation owing to the chloride-carbonate liquid immiscibility since no such immiscibility was established. We also studied the interaction of the NaCl–CaCO3–MgCO3 system with iron metal and found that carbonate reduction produces C-bearing species (Fe0, Fe-C melt, Fe3C, Fe7C3, C0) and wüstite containing Na2O, CaO, and MgO. Besides, a carbonate chloride compound, Ca2Cl2CO3, was established among the reaction products. The interaction between NaCl-bearing carbonate melt shifts its composition toward Mg-poor and NaCl-rich. Given the above, an alternative hypothesis can be proposed, according to which the interaction of alkaline chloride-bearing carbonate melts formed in the subduction zones with the reduced mantle should be accompanied by diamond crystallization and shift the composition of the melt from carbonatitic to alkali-rich saline.  相似文献   

3.
Lawsonite blueschists are important markers of cold subduction zones, subjected to intense fluid circulation. This is because lawsonite preservation in exhumed blueschists and eclogites is typically linked to cold exhumation paths, accompanied by hydration. In the Catena Costiera (Calabria, southern Italy), lawsonite–clinopyroxene blueschists of the Diamante–Terranova Unit, affected by ductile shearing and retrogression, are exposed. Blueschists contain zoned clinopyroxene crystals, showing core–rim compositional variation from diopside to omphacite and hosting primary inclusions of lawsonite and titanite. Thermodynamic modelling of phase equilibria in the NCKFMASHTO system revealed peak metamorphic conditions of 2.0–2.1 GPa and 475–490°C for the Alpine subduction in Calabria. The subsequent post-peak metamorphic evolution mainly proceeded along a decompression and cooling path up to ~1.1 GPa and ~380°C. The final exhumation stages are recorded in the sheared blueschists where a mylonitic to ultramylonitic foliation developed at ~0.7 GPa and 290–315°C. Therefore, the P–T evolution of the Diamante–Terranova blueschists mostly occurred in the stability field of lawsonite, sustained by H2O-saturated conditions during the exhumation path. The results of this study indicate that the blueschists underwent peak metamorphic conditions higher than previously thought, reaching a maximum depth of ~70 km under a very cold geothermal gradient (~6.6°C/km), during the Eocene subduction of the Ligurian Tethys oceanic crust in Calabria.  相似文献   

4.
The beginnings of hydrous mantle wedge melting   总被引：5，自引：3，他引：2  
This study presents new phase equilibrium data on primitive mantle peridotite (0.33 wt% Na2O, 0.03 wt% K2O) in the presence of excess H2O (14.5 wt% H2O) from 740 to 1,200°C at 3.2–6 GPa. Based on textural and chemical evidence, we find that the H2O-saturated peridotite solidus remains isothermal between 800 and 820°C at 3–6 GPa. We identify both quenched solute from the H2O-rich fluid phase and quenched silicate melt in supersolidus experiments. Chlorite is stable on and above the H2O-saturated solidus from 2 to 3.6 GPa, and chlorite peridotite melting experiments (containing ~6 wt% chlorite) show that melting occurs at the chlorite-out boundary over this pressure range, which is within 20°C of the H2O-saturated melting curve. Chlorite can therefore provide sufficient H2O upon breakdown to trigger dehydration melting in the mantle wedge or perpetuate ongoing H2O-saturated melting. Constraints from recent geodynamic models of hot subduction zones like Cascadia suggest that significantly more H2O is fluxed from the subducting slab near 100 km depth than can be bound in a layer of chloritized peridotite ~ 1 km thick at the base of the mantle wedge. Therefore, the dehydration of serpentinized mantle in the subducted lithosphere supplies free H2O to trigger melting at the H2O-saturated solidus in the lowermost mantle wedge. Alternatively, in cool subduction zones like the Northern Marianas, a layer of chloritized peridotite up to 1.5 km thick could contain all the H2O fluxed from the slab every million years near 100 km depth, which suggests that the dominant form of melting below arcs in cool subduction zones is chlorite dehydration melting. Slab P–T paths from recent geodynamic models also allow for melts of subducted sediment, oceanic crust, and/or sediment diapirs to interact with hydrous mantle melts within the mantle wedge at intermediate to hot subduction zones.  相似文献   

5.
We have experimentally investigated melting phase relation of a nominally anhydrous, carbonated pelitic eclogite (HPLC1) at 2.5 and 3.0 GPa at 900–1,350°C in order to constrain the cycling of sedimentary carbon in subduction zones. The starting composition HPLC1 (with 5 wt% bulk CO2) is a model composition, on a water-free basis, and is aimed to represent a mixture of 10 wt% pelagic carbonate unit and 90 wt% hemipelagic mud unit that enter the Central American trench. Sub-solidus assemblage comprises clinopyroxene + garnet + K-feldspar + quartz/coesite + rutile + calcio-ankerite/ankeritess. Solidus temperature is at 900–950°C at 2.5 GPa and at 900–1,000°C at 3.0 GPa, and the near-solidus melt is K-rich granitic. Crystalline carbonates persist only 50–100°C above the solidus and at temperatures above carbonate breakdown, carbon exists in the form of dissolved CO2 in silica-rich melts and as a vapor phase. The rhyodacitic to dacitic partial melt evolves from a K-rich composition at near-solidus condition to K-poor, and Na- and Ca-rich composition with increasing temperature. The low breakdown temperatures of crystalline carbonate in our study compared to those of recent studies on carbonated basaltic eclogite and peridotite owes to Fe-enrichment of carbonates in pelitic lithologies. However, the conditions of carbonate release in our study still remain higher than the modern depth-temperature trajectories of slab-mantle interface at sub-arc depths, suggesting that the release of sedimentary carbonates is unlikely in modern subduction zones. One possible scenario of carbonate release in modern subduction zones is the detachment and advection of sedimentary piles to hotter mantle wedge and consequent dissolution of carbonate in rhyodacitic partial melt. In the Paleo-NeoProterozoic Earth, on the other hand, the hotter slab-surface temperatures at subduction zones likely caused efficient liberation of carbon from subducting sedimentary carbonates. Deeply subducted carbonated sediments, similar to HPLC1, upon encountering a hotter mantle geotherm in the oceanic province can release carbon-bearing melts with high K2O, K2O/TiO2, and high silica, and can contribute to EM2-type ocean island basalts. Generation of EM2-type mantle end-member may also occur through metasomatism of mantle wedge by carbonated metapelite plume-derived partial melts.  相似文献   

6.
The pressure–temperature conditions of the reactions of the double carbonates CaM(CO3)2, where M = Mg (dolomite), Fe (ankerite) and Mn (kutnohorite), to MCO3 plus CaCO3 (aragonite) have been investigated at 5–8 GPa, 600–1,100°C, using multi-anvil apparatus. The reaction dolomite = magnesite + aragonite is in good agreement with the results of Sato and Katsura (Earth Planet Sci 184:529–534, 2001), but in poor agreement with the results of Luth (Contrib Mineral Petrol 141:222–232, 2001). The dolomite is partially disordered at 620°C, and fully disordered at 1,100°C. All ankerite and kutnohorite samples, including the synthetic starting materials, are disordered. The P–T slopes of the three reactions increase in the order M = Mg, Fe, Mn. The shallower slope for the reaction involving magnesite is due partly to its having a higher compressibility than expected from unit-cell volume considerations. At low pressures there is a preference for partitioning into the double carbonate of Mg > Fe > Mn. At high pressures the partitioning preference is reversed. Using the measured reaction positions, the P–T conditions at which dolomite solid solutions will break down on increasing P and T in subduction zones can be estimated.  相似文献   

7.
The melting behaviour of three carbonated pelites containing 0–1 wt% water was studied at 8 and 13 GPa, 900–1,850°C to define conditions of melting, melt compositions and melting reactions. At 8 GPa, the fluid-absent and dry carbonated pelite solidi locate at 950 and 1,075°C, respectively; >100°C lower than in carbonated basalts and 150–300°C lower than the mantle adiabat. From 8 to 13 GPa, the fluid-present and dry solidi temperatures then increase to 1,150 and 1,325°C for the 1.1 wt% H2O and the dry composition, respectively. The melting behaviour in the 1.1 wt% H2O composition changes from fluid-absent at 8 GPa to fluid-present at 13 GPa with the pressure breakdown of phengite and the absence of other hydrous minerals. Melting reactions are controlled by carbonates, and the potassium and hydrous phases present in the subsolidus. The first melts, which composition has been determined by reverse sandwich experiments, are potassium-rich Ca–Fe–Mg-carbonatites, with extreme K2O/Na2O wt ratios of up to 42 at 8 GPa. Na is compatible in clinopyroxene with D\textNa\textcpx/\textcarbonatite = 10-18 D_{\text{Na}}^{{{\text{cpx}}/{\text{carbonatite}}}} = 10{-}18 at the solidus at 8 GPa. The melt K2O/Na2O slightly decreases with increasing temperature and degree of melting but strongly decreases from 8 to 13 GPa when K-hollandite extends its stability field to 200°C above the solidus. The compositional array of the sediment-derived carbonatites is congruent with alkali- and CO2-rich melt or fluid inclusions found in diamonds. The fluid-absent melting of carbonated pelites at 8 GPa contrasts that at ≤5 GPa where silicate melts form at lower temperatures than carbonatites. Comparison of our melting temperatures with typical subduction and mantle geotherms shows that melting of carbonated pelites to 400-km depth is only feasible for extremely hot subduction. Nevertheless, melting may occur when subduction slows down or stops and thermal relaxation sets in. Our experiments show that CO2-metasomatism originating from subducted crust is intimately linked with K-metasomatism at depth of >200 km. As long as the mantle remains adiabatic, low-viscosity carbonatites will rise into the mantle and percolate upwards. In cold subcontinental lithospheric mantle keels, the potassic Ca–Fe–Mg-carbonatites may freeze when reacting with the surrounding mantle leading to potassium-, carbonate/diamond- and incompatible element enriched metasomatized zones, which are most likely at the origin of ultrapotassic magmas such as group II kimberlites.  相似文献   

8.
We determined the forward rate constant (K+) for the Fe2+–Mg order–disorder between the M2 and M1 sites of orthopyroxene (OPx), which is described by the homogeneous reaction Fe2+ (M2) + Mg(M1) ↔ Mg(M2) + Fe2+ (M1), by both ordering and disordering experiments at isothermal condition and also by continuous cooling experiments. The rate constant was determined as a function of temperature in the range of 550–750°C, oxygen fugacity between quartz–fayalite–iron and Ni–NiO buffers, and at compositions of 16 and 50 mol% ferrosilite component. The K+ value derived from disordering experiment was found to be larger than that derived from ordering experiment at 550°C, while at T>580°C, these two values are essentially the same. The fO2 dependence of the rate constant can be described by the relation K+ α (fO2) n with n=5.5–6.5, which is compatible with the theoretically expected relation. The Arrhenius relation at the WI buffer condition is given by
where C o represents the total number of M2 + M1 sites occupied by Fe2+ and Mg per unit volume of the crystal. The above relation can be used to calculate the cooling rates of natural OPx crystals around the closure temperature (T c) of Fe–Mg ordering, which are usually below 300°C for slowly cooled rocks. We determined the Fe–Mg ordering states of several OPx crystals (∼ Fs50) from the Central Gneissic Complex (Khtada Lake), British Columbia, which yields T c ∼290°C. Numerical simulation of the change of Fe2+-Mg ordering in OPx as a function of temperature using the above expression of rate constant and a non-linear cooling model yields quenched values of ordering states that are in agreement with the observed values for cooling rates of 11–17°C/Myr below 300°C. The inferred cooling rate is in agreement with the available geochronological constraints.  相似文献   

9.
Piston cylinder experiments were performed to constrain the pressure and temperature conditions for two high-pressure antigorite dehydration reactions found in silica-enriched serpentinites from Cerro del Almirez (Nevado–Filábride Complex, Betic Cordillera, southern Spain). At 630–660°C and pressures greater than 1.6 GPa, antigorite first reacts with talc to form orthopyroxene ± chlorite + fluid. We show that orthopyroxene + antigorite is restricted to high-pressure metamorphism of silica-enriched serpentinite. This uncommon assemblage is helpful in constraining metamorphic conditions in cold subduction environments, where antigorite serpentinites have no diagnostic assemblages over a large pressure and temperature range. The second dehydration reaction leads to the breakdown of antigorite to olivine + orthopyroxene + chlorite + fluid. The maximum stability of antigorite is found at 680°C at 1.9 GPa, which also corresponds to the maximum pressure limit for tremolite coexisting with olivine + orthopyroxene. The high aluminium (3.70 wt% Al2O3) and chromium contents (0.59 wt% Cr2O3) of antigorite in the investigated starting material is responsible for the expansion of the serpentinite stability to 60–70°C higher temperatures at 1.8 GPa than the antigorite stability calculated in the Al-free system. The antigorite from our study has the highest Al–Cr contents among all experimental studies and therefore likely constraints the maximum stability of antigorite in natural systems. Comparison of experimental results with olivine–orthopyroxene–chlorite–tremolite assemblages outcropping in Cerro del Almirez indicates that peak metamorphic conditions were 680–710°C and 1.6–1.9 GPa.  相似文献   

10.
The kinetics of non-convergent cation ordering in MgFe2O4 have been studied by measuring the Curie temperature (T c) of synthetic samples as a function of isothermal annealing time. The starting material was a synthetic sample of near-stoichiometric MgFe2O4, synthesised from the oxides in air and quenched from 900 °C in water. Ordering experiments were performed using small chips of this material and annealing them at temperatures between 450 °C and 600 °C. The chips were periodically removed from the furnace, and their Curie temperatures were determined from measurements of alternating-field magnetic susceptibility (χ) as a function of temperature (T) to 400 °C. The Curie temperature of MgFe2O4 is very sensitive to the intracrystalline distribution of Fe3+ and Mg cations between tetrahedral and octahedral sites of the spinel crystal structure, and hence provides a very sensitive probe of the cation ordering process. The χ-T curve for the starting material displays a single sharp magnetic transition at a temperature of 303 °C. During isothermal annealing, the χ-T curve develops two distinct magnetic transitions; the first at a temperature corresponding to T c for the disordered starting material and the second at a higher temperature corresponding to T c for the equilibrium ordered phase. The size of the magnetic signal from the ordered phase increases smoothly as a function of time, until equilibrium is approached and the shape of the χ-T curve corresponds to a single sharp magnetic transition for the homogeneous ordered phase. These observations demonstrate that cation ordering in MgFe2O4 proceeds via a heterogeneous mechanism, involving the nucleation and growth of fine-scale domains of the ordered phase within a matrix of disordered material. Disordering experiments were performed by taking material equilibrated at 558 °C and annealing it at 695 °C. The mechanism of isothermal disordering is shown to involve nucleation and growth of disordered domains within an ordered matrix, combined with continuous disordering of the ordered matrix. This mixed mechanism of disordering may provide an explanation for the difference between the rates of ordering and disordering observed in MgFe2O4 using X-ray diffraction. The origin of the heterogeneous ordering/disordering mechanism is discussed in terms of the Ginzburg-Landau rate law. It is argued that heterogeneous mechanisms are likely to occur in kinetic experiments performed far from equilibrium, whereas a homogeneous mechanism may operate under slow equilibrium cooling. The implications of these observations for geospeedometry are discussed. Received: 12 May 1998 / Accepted: 25 June 1998  相似文献   

11.
Pressure–temperature conditions of tourmaline breakdown in a metapelite were determined by high-pressure experiments at 700–900°C and 4–6 GPa. These experiments produced an eclogite–facies assemblage of garnet, clinopyroxene, phengite, coesite, kyanite and rare rutile. The modal proportions of tourmaline clearly decreased between 4.5 and 5 GPa at 700°C, between 4 and 4.5 GPa at 800°C, and between 800 and 850°C at 4 GPa, with tourmaline that survived the higher temperature conditions appearing corroded and thus metastable. Decreases in the modal abundance of tourmaline are accompanied by decreasing modal abundance of coesite, and increasing that of clinopyroxene, garnet and kyanite; the boron content of phengite increases significantly. These changes suggest that, with increasing pressure and temperature, tourmaline reacts with coesite to produce clinopyroxene, garnet, kyanite, and boron-bearing phengite and fluid. Our results suggest that: (1) tourmaline breakdown occurs at lower pressures and temperatures in SiO2-saturated systems than in SiO2-undersaturated systems. (2) In even cold subduction zones, subducting sediments should release boron-rich fluids by tourmaline breakdown before reaching depths of 150 km, and (3) even after tourmaline breakdown, a significant amount of boron partitioned into phengite could be stored in deeply subducted sediments.  相似文献   

12.
Lower crustal xenoliths erupted from an intraplate diatreme reveal that a portion of the New Zealand Gondwana margin experienced high‐temperature (HT) to ultrahigh‐temperature (UHT) granulite facies metamorphism just after flat slab subduction ceased at c. 110–105 Ma. P–T calculations for garnet–orthopyroxene‐bearing felsic granulite xenoliths indicate equilibration at ~815 to 910°C and 0.7 to 0.8 GPa, with garnet‐bearing mafic granulite xenoliths yielding at least 900°C. Supporting evidence for the attainment of HT and UHT conditions in felsic granulite comes from re‐integration of exsolution in feldspar (~900–950°C at 0.8 GPa), Ti‐in‐zircon thermometry on Y‐depleted overgrowths on detrital zircon grains (932°C ± 24°C at aTiO2 = 0.8 ± 0.2), and correlation of observed assemblages and mineral compositions with thermodynamic modelling results (≥850°C at 0.7 to 0.8 GPa). The thin zircon overgrowths, which were mainly targeted by drilling through the cores of grains, yield a U–Pb pooled age of 91.7 ± 2.0 Ma. The cause of Late Cretaceous HT‐UHT metamorphism on the Zealandia Gondwana margin is attributed to collision and partial subduction of the buoyant oceanic Hikurangi Plateau in the Early Cretaceous. The halt of subduction caused the fore‐running shallowly dipping slab to rollback towards the trench position and permitted the upper mantle to rapidly increase the geothermal gradient through the base of the extending (former) accretionary prism. This sequence of events provides a mechanism for achieving regional HT–UHT conditions in the lower crust with little or no sign of this event at the surface.  相似文献   

13.
The reaction glaucophane + 2 diopside + 2 quartz = tremolite + 2 albite is proposed to model the transition from the blueschist to greenschist facies. This reaction was investigated experimentally over the range of 1.0–2.1 GPa and 500–800°C using synthetic phases in the chemical system Na2O–CaO–MgO–Al2O3–SiO2–H2O. Reversals of this reaction were possible at 500 and 550°C and growth of the low-pressure assemblage at 600°C; however, at temperatures of 600°C and higher and at pressures above 1.6 GPa omphacite nucleation (at the expense of diopside and albite) became quite strong and prevented attaining clear reversals of this reaction. Compositional changes in the amphiboles were determined by both electron microprobe analyses and correlations between unit-cell dimensions and composition. Glaucophane and particularly tremolite showed clear signs of compositional re-equilibration and merged to a single amphibole of winchite composition by about 754°C. These data were used to model the miscibility gap between glaucophane and tremolite using either the asymmetric multicomponent formulism parameters of W TR,GL of 68 kJ with αTR of 1.0 and αGL of 0.75 or a simple two-site asymmetric thermodynamic mixing expression with Margules parameters W NaCa of 13.4 kJ and W CaNa of 19.3 kJ. Combination of these thermodynamic models of the miscibility gap with extant thermodynamic data for the other phases yields a calculated location of the above reaction, involving pure diopside and albite, that is in good agreement with the observed experimental reversals and amphibole compositions over the range of 0.94–1.93 GPa and 400–754°C. The calculated effect of jadeite solid solution into diopside is to reduce the dP/dT slope from 0.0028 to 0.0021 GPa/°C and decrease the pressure by 0.28 GPa at 754°C. The dP/dT slope of this reaction boundary lies close to a linear geotherm of 13°C/km and is consistent with the slopes of other solid–solid reactions that have been used to model the blueschist-to-greenschist facies transition.  相似文献   

14.
Lawsonite eclogite and garnet blueschist occur as metre-scale blocks within serpentinite mélange in the southern New England Orogen (SNEO) in eastern Australia. These high-P fragments are the products of early Palaeozoic subduction of the palaeo-Pacific plate beneath East Gondwana. Lu–Hf, Sm–Nd, and U–Pb geochronological data from Port Macquarie show that eclogite mineral assemblages formed between c. 500 and 470 Ma ago and became mixed together within a serpentinite-filled subduction channel. Age data and P–T modelling indicate lawsonite eclogite formed at ~2.7 GPa and 590°C at c. 490 Ma, whereas peak garnet in blueschist formed at ~2.0 GPa and 550°C at c. 470 Ma. The post-peak evolution of lawsonite eclogite was associated with the preservation of pristine lawsonite-bearing assemblages and the formation of glaucophane. By contrast, the garnet blueschist was derived from a precursor garnet–omphacite assemblage. The geochronological data from these different aged high-P assemblages indicate the high-P rocks were formed during subduction on the margin of cratonic Australia during the Cambro-Ordovician. The rocks however now reside in the Devonian–Carboniferous southern SNEO, which forms the youngest and most outboard of the eastern Gondwanan Australian orogenic belts. Geodynamic modelling suggests that over the time-scales that subduction products accumulated, the high-P rocks migrated large distances (~>1,000 km) during slab retreat. Consequently, high-P rocks that are trapped in subduction channels may also migrate large distances prior to exhumation, potentially becoming incorporated into younger orogenic belts whose evolution is not directly related to the formation of the exhumed high-P rocks.  相似文献   

15.
Metamorphic diamond in crustal rocks provides important information on the deep subduction of continental crust. Here, we present a new occurrence of diamond within the Seve Nappe Complex (SNC) of the Scandinavian Caledonides, on Åreskutan in Jämtland County, Sweden. Microdiamond is found in situ as single and composite (diamond+carbonate) inclusions within garnet, in kyanite‐bearing paragneisses. The rocks preserve the primary peak pressure assemblage of Ca,Mg‐rich garnet+phengite+kyanite+rutile, with polycrystalline quartz surrounded by radial cracks indicating breakdown of coesite. Calculated P–T conditions for this stage are 830–840 °C and 4.1–4.2 GPa, in the diamond stability field. The ultrahigh‐pressure (UHP) assemblage has been variably overprinted under granulite facies conditions of 850–860 °C and 1.0–1.1 GPa, leading to formation of Ca,Mg‐poor garnet+biotite+plagioclase+K‐feldspar+sillimanite+ilmenite+quartz. This overprint was the result of nearly isothermal decompression, which is corroborated by Ti‐in‐quartz thermometry. Chemical Th–U–Pb dating of monazite yields ages between 445 and 435 Ma, which are interpreted to record post‐UHP exhumation of the diamond‐bearing rocks. The new discovery of microdiamond on Åreskutan, together with other evidence of ultrahigh‐pressure metamorphism (UHPM) within gneisses, eclogites and peridotites elsewhere in the SNC, provide compelling arguments for regional (at least 200 km along strike of the unit) UHPM of substantial parts of this far‐travelled allochthon. The occurrence of UHPM in both rheologically weak (gneisses) and strong lithologies (eclogites, peridotites) speaks against the presence of large tectonic overpressure during metamorphism.  相似文献   

16.
Phase relations of phlogopite with magnesite from 4 to 8 GPa   总被引：2，自引：2，他引：0  
To evaluate the stability of phlogopite in the presence of carbonate in the Earth’s mantle, we conducted a series of experiments in the KMAS–H2O–CO2 system. A mixture consisting of synthetic phlogopite (phl) and natural magnesite (mag) was prepared (phl90-mag10; wt%) and run at pressures from 4 to 8 GPa at temperatures ranging from 1,150 to 1,550°C. We bracketed the solidus between 1,200 and 1,250°C at pressures of 4, 5 and 6 GPa and between 1,150 and 1,200°C at a pressure of 7 GPa. Below the solidus, phlogopite coexists with magnesite, pyrope and a fluid. At the solidus, magnesite is the first phase to react out, and enstatite and olivine appear. Phlogopite melts over a temperature range of ~150°C. The amount of garnet increases above solidus from ~10 to ~30 modal% to higher pressures and temperatures. A dramatic change in the composition of quench phlogopite is observed with increasing pressure from similar to primary phlogopite at 4 GPa to hypersilicic at pressures ≥5 GPa. Relative to CO2-free systems, the solidus is lowered such, that, if carbonation reactions and phlogopite metasomatism take place above a subducting slab in a very hot (Cascadia-type) subduction environment, phlogopite will melt at a pressure of ~7.5 GPa. In a cold (40 mWm−2) subcontinental lithospheric mantle, phlogopite is stable to a depth of 200 km in the presence of carbonate and can coexist with a fluid that becomes Si-rich with increasing pressure. Ascending kimberlitic melts that are produced at greater depths could react with peridotite at the base of the subcontinental lithospheric mantle, crystallizing phlogopite and carbonate at a depth of 180–200 km.  相似文献   

17.
《Precambrian Research》2004,132(4):327-348
The Saramta massif in the Paleoproterozoic Sharyzhalgai complex, the southwestern margin of the Siberian craton, is mainly composed of spinel-peridotites with garnet-websterites; it is enclosed within granitic gneisses and migmatites with mafic intercalations of granulite-facies grade. The garnet-websterites occur as lenses or layers intercalated within spinel-harzburgite and spinel-lherzolite. They consist mainly of clinopyroxene (Cpx), garnet (Grt), and orthopyroxene (Opx): Grt often includes Cpx, Opx, and pargasite (Prg). Opx also occurs as kelyphite with plagioclase (Pl), spinel, olivine, Prg, and biotite. Relationships between textures and chemical compositions of these minerals suggest the following P–T stages: stage 1 (pre-peak), 0.9–1.5 GPa at 640–780 °C; stage 2 (peak), 2.3–3.0 GPa at 920–1030 °C as the minimum estimate; and stage 3 (post-peak), 750–830 °C at 0.5–0.9 GPa. Finally, the garnet-websterites are veined with lower amphibolite- to greenschist-facies minerals (stage 4).These results suggests that the Saramta massif was carried to depths of c. 100 km by subduction, and metamorphosed under eclogite-facies conditions in the Paleoproterozoic, despite the commonly held view that high geothermal gradients in those times would have prevented such deep subduction. Paleoproterozoic plate subduction at the southwestern margin of the Siberian craton might have caused subduction-zone magmatism and mantle metasomatism similar to those in the Phanerozoic.  相似文献   

18.
The first evidence for ultrahigh-pressure (UHP) metamorphism in the Seve Nappe Complex of the Scandinavian Caledonides is recorded by kyanite-bearing eclogite, found in a basic dyke within a garnet peridotite body exposed close to the lake Friningen in northern Jämtland (central Sweden). UHP metamorphic conditions of ~ 3 GPa and 800 °C, within the stability field of coesite, are constrained from geothermobarometry and calculated phase equilibria for the peak-pressure assemblage garnet + omphacite + kyanite + phengite. A prograde metamorphic evolution from a lower P–T (1.5–1.7 GPa and 700–750 °C) stage during subduction is inferred from inclusions of pargasitic amphibole, zoisite and kyanite in garnet cores. The post-UHP evolution is constrained from breakdown textures, such as exsolutions of kyanite and silica from the Ca-Eskola clinopyroxene. Near isothermal decompression of eclogite to lower crustal levels (~ 0.8–1.0 GPa ) led to formation of sapphirine, spinel, orthopyroxene and diopside at granulite facies conditions. Published age data suggest a Late Ordovician (460–445 Ma) age of the UHP metamorphism, interpreted to be related to subduction of Baltoscandian continental margin underneath an outboard terrane, possibly outermost Laurentia, during the final stages of closure of the Iapetus Ocean. The UHP rocks were emplaced from the hinterland collision zone during Scandian thrusting of the nappes onto the Baltoscandian foreland basin and platform. The record of P–T conditions and geochonological data from UHP rocks occurring within the allochthonous units of the Scandinavian Caledonides indicate that Ordovician UHP events may have affected much wider parts of the orogen than previously thought, involving deep subduction of the continental crust prior to final Scandian collision between Baltica and Laurentia.  相似文献   

19.
Understanding convergent margin processes requires determination of the onset and the termination of subduction, the duration of subduction‐zone metamorphism, and the subduction zone polarity. Garnet growth and intracrystalline zonation can be used to constrain the timing, duration and kinetics of tectonometamorphic processes. An eclogite from the Huwan shear zone in the Hong'an orogen was investigated with combined pseudosection analysis and multiple geochronologies. The pseudosection analysis illustrates that garnet growth is continuous and along an early near‐isothermal trajectory followed by a near‐isobaric heating path from 1.9 GPa/500 °C to 2.4 GPa/575 °C and subsequent near‐isothermal decompression. 40Ar/39Ar dating of an amphibole inclusion in garnet from the eclogite yielded an age of 310 ± 5 Ma, which is consistent with a U–Pb age of 305 ± 3 Ma for the metamorphic zircon within uncertainty. Garnet core and rim material produced Lu–Hf ages of 296.9 ± 3.8 and 256.9 ± 3.9 Ma respectively; the latter is consistent with its Sm–Nd age of 254.3 ± 4.6 Ma for the same aliquots. Similarly, limited zircon U–Pb ages of c. 257 Ma were obtained in zircon rims with garnet inclusions. These ages were interpreted to bracket the period of garnet growth and the difference of up to c. 40 Ma is best explained by protracted garnet growth. We propose that the rocks represent detachment of part of the downgoing slab and remained free of significant compression/decompression or heating/cooling close to the subduction channel, most likely underplating the mantle wedge, for a long time. These rocks were incorporated into the following subduction channel due to the successive entry of the buoyant materials, and exhumed at some time later than c. 254 Ma. The increasing observations of protracted garnet growth and long‐lived subduction in various orogens worldwide demand more sophisticated geodynamic models.  相似文献   

20.
High-pressure (HP) granulites provide telling records of mineral reactions at upper mantle to lower crustal levels and key information on the fate of material in subduction systems. The latter especially applies when they abut eclogite and mantle dunite because such rock associations are crucial for understanding the incompletely known processes at the interface of converging plates. A continental arc, active c. 520–395 Ma ago, formed an enigmatic example of such a rock association in the Songshugou area, Qinling Orogen. To unravel the juxtaposition of the distinct rocks, this study combines petrography, phase equilibria modelling, conventional thermobarometry, and zircon U–Th–Pb–Ti–REE analysis. Two mafic HP granulites, which contain the mineral assemblages garnet–clinopyroxene–plagioclase–rutile–mesoperthite–quartz and garnet–clinopyroxene–plagioclase–rutile, experienced peak metamorphic conditions of ≤1.4 GPa, 860°C and ~1.3 GPa, ≥910°C, respectively. During decompression and cooling, at 489 ± 4 Ma, amphibole lamellae unmixed from a clinopyroxene solid solution and orthopyroxene in part replaced garnet. A felsic HP granulite shows equilibration of garnet, perthite, antiperthite, kyanite, quartz, and rutile at 810–860°C, ~1.2 GPa, sillimanite growth during decompression, and upper amphibolite facies cooling at 510 ± 4 Ma. Though the thermobarometric data are just within the methodological errors, the U/Pb zircon ages imply the HP granulites did not evolve coherently. The HP granulites either represent foundered lower arc crust or originated from subduction erosion because their geochemistry is indistinguishable from that of the hanging-wall plate. Published and new pressure–temperature–time–deformation paths converge at ~710°C, ~0.9 GPa, and ≲470 Ma, implying exhumation tectonics juxtaposed the HP granulites with a mélange of eclogite and mantle dunite at lower crustal levels. This study highlights that lower arc crust can comprise material of diverse evolution.  相似文献   

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