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1.
《Geodinamica Acta》2013,26(5):323-343
A multiequilibrium thermobarometric approach was used to estimate the P-T conditions of successive metamorphic stages in carpholite-bearing blueschists that occur at the base of the Phyllite - Quartzite nappe of Peloponnese, in contact with the Ionian Plattenkalk. The calculated P-T conditions for successive metamorphic stages correlate well in samples from two different areas. A retrograde P-T path can be calculated, evolving from ~14 kbar, 400-450°C for chloritoid-bearing (carpholite-free) parageneses, to 11-13 kbar, 320-380°C for chloritoid + Mgcarpholite parageneses, ~7.5 kbar, 260-275°C for Mg-carpholite + sudoite parageneses, and ~3-4 kbar, ~250°C for parageneses involving only phyllosilicates. Thermobarometric calculations suggest that Mg-carpholite is a retrograde phase in the Peloponnese. This feature has never been observed elsewhere in high pressure-low temperature carpholite-bearing schists. The calculated P-T paths indicate that the Mgcarpholite blueschists were subducted to ~40km depth and maintained in a cool thermal gradient of ~7°C/km during exhumation.  相似文献   

2.
Fluid inclusions and geological relationships indicate that rodingite formation in the Asbestos ophiolite, Québec, occurred in two, or possibly three, separate episodes during thrusting of the ophiolite onto the Laurentian margin, and that it involved three fluids. The first episode of rodingitization, which affected diorite, occurred at temperatures of between 290 and 360°C and pressures of 2.5 to 4.5 kbar, and the second episode, which affected granite and slate, occurred at temperatures of between 325 and 400°C and pressures less than 3 kbar. The fluids responsible for these episodes of alteration were moderately to strongly saline (~1.5 to 6.3 m eq. NaCl), rich in divalent cations and contained appreciable methane. A possible third episode of alteration is suggested by primary fluid inclusions in vesuvianite-rich bodies and secondary inclusions in other types of rodingite, with significantly lower trapping temperatures, salinity and methane content. The association of the aqueous fluids with hydrocarbon-rich fluids containing CH4 and higher order alkanes, but no CO2, suggests strongly that the former originated from the serpentinites. The similarities in the composition of the fluids in all rock types indicate that the ophiolite had already been thrust onto the slates when rodingitization occurred.  相似文献   

3.
We report the first occurrence of poly-cyclic high-pressure low-temperature (HP-LT) rocks from the easternmost Indus-Yarlung suture zone, formed during subduction of Neo-Tethyan oceanic lithosphere. Petrology, mineral composition and P–T pseudosection modelling reveal two low-temperature eclogite facies metamorphic events with an initial high-pressure P–T condition of 16.4–18.7 kbar and 510–520°C, exhumation to 10.5–12.0 kbar and 580–590°C and a subsequent second high-pressure P–T condition of ~16 kbar and ~560°C and exhumation to ≤9 kbar and ≤600°C. This history implies a complex ‘yo-yo type’ P–T path. In situ monazite dating and textural relationships show that late-stage exhumation, cooling and garnet breakdown occurred at c. ~25–22 Ma. We interpret the first burial event to represent subduction of the Neo-Tethys Ocean at the eastern Indus-Yarlung suture zone. Initial exhumation, reburial and final exhumation represent material transport in a large-scale convective circulation system in the subduction channel. Convective overturn in the subduction channel evidently serves both as a mechanism to produce poly-cyclic metamorphism and to exhume LT eclogite facies rocks.  相似文献   

4.
The join tremolite (Tr)-pargasite (Pa) has been studied in the temperature range 750 °–1,150 ° C under a water vapor pressure of 1 and 5 kbar. There is a continuous solid solution series between the compositions Tr85Pa15 and TroPa100 at 850 ° C and 5 kbar. Tremolite and pargasite are separated by a solvus at 1 kbar and the field of tremolitic amphibole +pargasitic amphibole+vapor is present in the region between Tr90Pa10 and Tr10Pa90 at 800 ° C. The phase assemblages at 850 ° C and 1 kbar change as follows with increasing pargasite component; clinopyroxene +orthopyroxene+quartz+vapor, tremolitic amphibole+vapor, tremolitic amphibole+clinopyroxene +forsterite+plagioclase+vapor, tremolitic amphibole+pargasitic amphibole+vapor, and pargasitic amphibole+vapor. The petrological significance of amphibole pairs in metamorphic rocks is discussed on the basis of the experimental results.  相似文献   

5.
 Melting relations on the enstatite−diopside (En, Mg2Si2O6−Di, CaMgSi2O6) join, including the compositions of crystalline phases and melts coexisting along the solidi, were experimentally determined in the pressure range 70–224 kbar with a split-sphere anvil apparatus (USSA-2000). Melting is peritectic in enstatite-rich compositions at 70–124 kbar (1840–2100° C) and eutectic at higher pressures, while the diopside-rich clinopyroxene melts azeotropically at 70–165 kbar and up to 300° C lower temperatures than the eutectic. Orthopyroxene is replaced with enstatite-rich clinopyroxene at 120 kbar and 2090°C. First garnet with 17 mol% Di forms on the solidus at 158 kbar and 2100° C. Two garnets coexist on the solidus at 165–183 kbar and 2100° C, garnet coexists with CaSiO3 perovskite at 183–224 kbar (2100–2230° C) and two coexisting perovskites are stable at higher pressures. The melting curve of diopside was determined at 80–170 kbar; the slope becomes negative at 140 kbar and 2155° C. At 170 kbar and 2100° C, diopside with 96% Di breaks down to garnet with 89% Di and CaSiO3 perovskite. The new data were used to calculate an improved temperature-pressure phase diagram for the CMAS system, which can be useful for estimating the mineralogy of the Earth's upper mantle. Received: 15 October 1994 / Accepted: 15 October 1995  相似文献   

6.
Orogenic gold vein deposits in the Xiaoqinling district are situated in a basement-cored uplift along the southern margin of the North China craton. The deposits are hosted by Late Archean to Paleoproterozoic amphibolite-facies country rocks, varying in lithology from clastic and chemical sedimentary units to felsic and mafic volcanic rocks and plutons. Absolute and relative age relationships indicate a late Mesozoic emplacement of the lodes, which is subsequent to the deformation associated with the Middle to Late Triassic Qinling orogen along the craton margin. All auriferous quartz veins are hosted in faults. The ores are generally composed of quartz veins with various amounts of pyrite, galena, chalcopyrite, sphalerite, and carbonates. Mineralization can be separated into three distinct stages.

Ore fluids are H2O dominant, with approximately 20 to 30 and 10 to 20 mole% CO2 for gold-bearing stage I and II veins, respectively. Vein formation pressures and temperatures were 2.2 kbar and 300 to 370°C for stage I and 1.6 kbar and 250 to 320°C for stage II. The narrow range of δ18O values for ore fluids from the deposits throughout the Xiaoqinling district indicate a common deep fluid source, most likely of magmatic origin. The 34S data suggest sulfur originated from a magmatic fluid of approximately 2 ± 2%, with significant local sulfur contributions leading to large variations in the ore-stage sulfide minerals. The most probable mechanism for the deposition of gold is phase separation caused by the partial loss of volatiles such as CO2 and CH4.  相似文献   

7.
The Palaeo‐Mesoproterozoic metapelite granulites from northern Garo Hills, western Shillong‐Meghalaya Gneissic Complex (SMGC), northeast India, consist of resorbed garnet, cordierite and K‐feldspar porphyroblasts in a matrix comprising shape‐preferred aggregates of biotite±sillimanite+quartz that define the penetrative gneissic fabric. An earlier assemblage including biotite and sillimanite occurs as inclusions within the garnet and cordierite porphyroblasts. Staurolite within cordierite in samples without matrix sillimanite is interpreted to have formed by a reaction between the sillimanite inclusion and the host cordierite during retrogression. Accessory monazite occurs as inclusions within garnet as well as in the matrix, whereas accessory xenotime occurs only in the matrix. The monazite inclusions in garnet contain higher Ca, and lower Y and Th/U than the matrix monazite outside resorbed garnet rims. On the other hand, matrix monazite away from garnet contains low Ca and Y, and shows very high Th/U ratios. The low Th/U ratios (<10) of the Y‐poor garnet‐hosted monazite indicate subsolidus formation during an early stage of prograde metamorphism. A calculated P–T pseudosection in the MnCKFMASH‐PYCe system indicates that the garnet‐hosted monazite formed at <3 kbar/600 °C (Stage A). These P–T estimates extend backward the previously inferred prograde P–T path from peak anatectic conditions of 7–8 kbar/850 °C based on major mineral equilibria. Furthermore, the calculated P–T pseudosections indicate that cordierite–staurolite equilibrated at ~5.5 kbar/630 °C during retrograde metamorphism. Thus, the P–T path was counterclockwise. The Y‐rich matrix monazite outside garnet rims formed between ~3.2 kbar/650 °C and ~5 kbar/775 °C (Stage B) during prograde metamorphism. If the effect of bulk composition change due to open system behaviour during anatexis is considered, the P–T conditions may be lower for Stage A (<2 kbar/525 °C) and Stage B (~3 kbar/600 °C to ~3.5 kbar/660 °C). Prograde garnet growth occurred over the entire temperature range (550–850 °C), and Stage‐B monazite was perhaps initially entrapped in garnet. During post‐peak cooling, the Stage‐B monazite grains were released in the matrix by garnet dissolution. Furthermore, new matrix monazite (low Y and very high Th/U ≤80, ~8 kbar/850–800 °C, Stage C), some monazite outside garnet rims (high Y and intermediate Th/U ≤30, ~8 kbar/800–785 °C, Stage D), and matrix xenotime (<785 °C) formed through post‐peak crystallization of melt. Regardless of textural setting, all monazite populations show identical chemical ages (1630–1578 Ma, ±43 Ma). The lithological association (metapelite and mafic granulites), and metamorphic age and P–T path of the northern Garo Hills metapelites and those from the southern domain of the Central Indian Tectonic Zone (CITZ) are similar. The SMGC was initially aligned with the southern parts of CITZ and Chotanagpur Gneissic Complex of central/eastern India in an ENE direction, but was displaced ~350 km northward by sinistral movement along the north‐trending Eastern Indian Tectonic Zone in Neoproterozoic. The southern CITZ metapelites supposedly originated in a back‐arc associated with subducting oceanic lithosphere below the Southern Indian Block at c. 1.6 Ga during the initial stage of Indian shield assembly. It is inferred that the SMGC metapelites may also have originated contemporaneously with the southern CITZ metapelites in a similar back‐arc setting.  相似文献   

8.
Robust quantification of pressure (P)–temperature (T) paths for subduction-related HP/UHP metamorphic rocks is fundamental in recognizing spatial changes in both the depth of detachment from the down-going plate and the thermal evolution of convergent margin sutures in orogenic belts. Although the Chinese southwestern (SW) Tianshan is a well-known example of an accretionary metamorphic belt in which HP/UHP metabasites occur in voluminous host metasedimentary schists, information about the P–T evolution of these rocks in the eastern segment is limited, precluding a full understanding of the development of the belt as a whole. In this study at Kekesu in the eastern segment of the SW Tianshan, we use microstructural evidence and phase equilibrium modelling to quantify the peak and retrograde P–T conditions from two lawsonite-bearing micaschists and an enclosed garnet–epidote blueschist; for two of the samples we also constrain the late prograde P–T path. In the two micaschist samples, relics of prograde lawsonite are preserved in quartz inclusions in garnet, whereas in the metabasite, polymineralic aggregates included in garnet are interpreted as pseudomorphs after lawsonite. For garnet micaschist TK21, which is mainly composed of garnet, phengite/paragonite, albite, chlorite, quartz and relict lawsonite, with accessary rutile, titanite and ilmenite, the maximum P–T conditions for the peak stage are 18.0–19.0 kbar at 480–485°C. During initial exhumation, the retrograde P–T path passed through metamorphic conditions of 15.0–17.0 kbar at 460–500°C. For garnet–glaucophane micaschist TK33, which is mainly composed of garnet, glaucophane, phengite/paragonite, albite, chlorite, quartz, relict lawsonite and minor epidote, with accessary titanite, apatite, ilmenite and zircon, the maximum P conditions for the peak stage are >24.0 kbar at 400–500°C. During exhumation, the P–T path passed through metamorphic conditions of 17.5–18.5 kbar at 485–495°C and 14.0–17.5 kbar at 460–500°C. For garnet–epidote blueschist TK37, which is mainly composed of garnet, glaucophane, epidote, phengite, chlorite, albite and quartz, with accessary titanite, apatite, ilmenite, zircon and calcite, the prograde evolution passed through metamorphic conditions of ~20.0 kbar at ~445°C to Pmax conditions of ~21.5 kbar at 450–460°C and Tmax conditions of 19.5–21.0 kbar at 490–520°C. During exhumation, the rock passed through metamorphic conditions of 17.5–19.0 kbar at 475–500°C, before recording P–T conditions of <17.5 kbar at <500°C. These results demonstrate that maximum recorded pressures for individual samples vary by as much as 6 kbar in the eastern segment of the SW Tianshan, which may suggest exhumation from different depths in the subduction channel. Furthermore, the three samples record similar P–T paths from ~17.0 to 15.0 kbar, which suggests they were juxtaposed at a similar depth along the subduction interface. We compare our new results with published information from eclogites in the same area before considering the wider implications of these data for the orogenic development of the belt as a whole.  相似文献   

9.
Fluid equilibria in the H2O-Na2SO4-SiO2 system were experimentally studied at 700 and 800°C and pressures of 1, 2, and 3 kbar using synthetic fluid inclusions in quartz. The obtained results indicated a heterogeneous state of fluid within the whole range of experimental parameters of this study. Sodium sulfate underwent high-temperature hydrolysis, whose products chemically reacted with quartz. As a result, a noncrystalline phase containing substantial amounts of silica was formed at a temperature of 800°C and a pressure of 3 kbar. This phase was observed in the inclusions as glass. The thermometric investigation of inclusions that trapped fluid phases immiscible under experimental conditions showed that they can, in turn, become heterogeneous at temperatures of approximately 200–400°C. Under such conditions, three or four noncrystalline phases can be in equilibrium.  相似文献   

10.
ABSTRACT Thermobarometric studies on various granulite facies areas along the Prydz Bay coast, East Antarctica (73°-79°E, 68°-70°S), show that, at around 1100 Ma, during a late Proterozoic orogeny, the rocks of the Larsemann Hills suffered a lower pressure metamorphic peak than the surrounding areas. Along the Prydz Bay coast, the rocks affected by this event include parts of the Vestfold Hills block plus all of the Rauer Group, the Larsemann Hills and the Munro Kerr Mountains. The dykes in the south-west corner of the Vestfold Hills were recrystallized during this event with little deformation at temperatures not quite as high as in the areas further south-west (650°C, 6.5 kbar) (Collerson et al., 1983), the Rauer Group was metamorphosed at 800°C and 7.5 kbar (Harley, 1987a), the Larsemann Hills at 750°C and 4.5 kbar, and the Munro Kerr Mountains probably at around 850°C and 5 kbar. Retrograde equilibration in the different areas occurred during decompression to about 10 km depth in all areas, followed by isobaric cooling at this depth. This paper shows that the peak metamorphism in the Larsemann Hills occurred at a pressure which is too low to have been the consequence of thermal relaxation of overthickened crust with normal mantle heat flow. Although other areas in Prydz Bay were metamorphosed at sufficiently high pressures so that their decompression paths are not inconsistent with a continental collision model, the inferred pre-metamorphic peak histories and the requirement of consistency with the Larsemann Hills, make it unlikely that collision followed by erosion-driven decompression is an appropriate model. We suggest that the thermal regime of the crust in the Larsemann Hills region was controlled by a perturbation in the asthenosphere, with magma invasion of the crust. We suggest that the 500 Ma event, represented in Prydz Bay by granitic outcrops at Landing Bluff and by several K/Ar ages from the Larsemann Hills area, was responsible for the final excavation of the terrane.  相似文献   

11.
 The beginning of dehydration melting in the tonalite system (biotite-plagioclase-quartz) is investigated in the pressure range of 2–12 kbar. A special method consisting of surrounding a crystal of natural plagioclase (An45) with a biotite-quartz mixture, and observing reactions at the plagioclase margin was employed for precise determination of the solidus for dehydration melting. The beginning of dehydration melting was worked out at 5 kbar for a range of compositions of biotite varying from iron-free phlogopite to iron-rich Ann70, with and without titanium, fluorine and extra aluminium in the biotite. The dehydration melting of phlogopite + plagioclase (An45) + quartz begins between 750 and 770°C at pressures of 2 and 5 kbar, at approximately 740°C at 8 kbar and between 700 and 730°C at 10 kbar. At 12 kbar, the first melts are observed at temperatures as low as 700°C. The data indicate an almost vertical dehydration melting solidus curve at low pressures which bends backward to lower temperatures at higher pressures (> 5 kbar). The new phases observed at pressures ≤ 10 kbar are melt + enstatite + clinopyroxene + potassium feldspar ± amphibole. In addition to these, zoisite was also observed at 12 kbar. With increasing temperature, phlogopite becomes enriched in aluminium and deficient in potassium. Substitution of octahedral magnesium by aluminium and titanium in the phlogopite, as well as substitution of hydroxyl by fluorine, have little effect on the beginning of dehydration melting temperatures in this system. The dehydration melting of biotite (Ann50) + plagioclase (An45) + quartz begins 50°C below that of phlogopite bearing starting composition. Solid reaction products are orthopyroxene + clinopyroxene + potassium feldspar ± amphibole. Epidote was also observed above 8 kbar, and garnet at 12 kbar (750°C). The experiments on the iron-bearing system performed at ≤ 5 kbar were buffered with NiNiO. The f O 2 in high pressure runs lies close to CoCoO. With the substitution of octahedral magnesium and iron by aluminium and titanium, and replacement of hydroxyl by fluorine in biotite, the beginning of dehydration melting temperatures in this system increase up to 780°C at 5 kbar, which is 70°C above the beginning of dehydration melting of the assemblage containing biotite (Ann50) of ideal composition. The dehydration melting at 5 kbar in the more iron-rich Ann70-bearing starting composition begins at 730°C, and in the Ann25-bearing assemblage at 710°C. This indicates that quartz-biotite-plagioclase assemblages with intermediate compositions of biotite (Ann25 and Ann50) melt at lower temperatures as compared to those containing Fe-richer or Mg-richer biotites. This study shows that the dehydration melting of tonalites may begin at considerably lower temperatures than previously thought, especially at high pressures (>5 kbar). Received: 27 December 1995 / Accepted: 7 May 1996  相似文献   

12.
The Sivrihisar Massif, Turkey, is comprised of blueschist and eclogite facies metasedimentary and metabasaltic rocks. Abundant metre‐ to centimetre‐scale eclogite pods occur in blueschist facies metabasalt, marble and quartz‐rich rocks. Sivrihisar eclogite contains omphacite + garnet + phengite + rutile ± glaucophane ± quartz + lawsonite and/or epidote. Blueschists contain sodic amphibole + garnet + phengite + lawsonite and/or epidote ± omphacite ± quartz. Sivrihisar eclogite and blueschist have similar bulk composition, equivalent to NMORB, but record different P–T conditions: ～26 kbar, 500 °C (lawsonite eclogite); 18 kbar, 600 °C (epidote eclogite); 12 kbar, 380 °C (lawsonite blueschist); and 15–16 kbar, 480–500 °C (lawsonite‐epidote blueschist). Pressures for the Sivrihisar lawsonite eclogite are among the highest reported for this rock type, which is rarely exposed at the Earth's surface. The distribution and textures of lawsonite ± epidote define P–T conditions and paths. For example, in some lawsonite‐bearing rocks, epidote inclusions in garnet and partial replacement of matrix epidote by lawsonite suggest an anticlockwise P–T path. Other rocks contain no epidote as inclusions or as a matrix phase, and were metamorphosed entirely within the lawsonite stability field. Results of the P–T study and mapping of the distribution of blueschists and eclogites in the massif suggest that rocks recording different maximum P–T conditions were tectonically juxtaposed as kilometre‐scale slices and associated high‐P pods, although all shared the same exhumation path from ～9–11 kbar, 300–400 °C. Within the tectonic slices, alternating millimetre–centimetre‐scale layers of eclogite and blueschist formed together at the same P–T conditions but represent different extents of prograde reaction controlled by strain partitioning or local variations in fO2 or other chemical factors.  相似文献   

13.
Rare ultrahigh‐temperature–(near)ultrahigh‐pressure (UHT–near‐UHP) crustal xenoliths erupted at 11 Ma in the Pamir Mountains, southeastern Tajikistan, preserve a compositional and thermal record at mantle depths of crustal material subducted beneath the largest collisional orogen on Earth. A combination of oxygen‐isotope thermometry, major‐element thermobarometry and pseudosection analysis reveals that, prior to eruption, the xenoliths partially equilibrated at conditions ranging from 815 °C at 19 kbar to 1100 °C at 27 kbar for eclogites and granulites, and 884 °C at 20 kbar to 1012 °C at 33 kbar for garnet–phlogopite websterites. To reach these conditions, the eclogites and granulites must have undergone mica‐dehydration melting. The extraction depths exceed the present‐day Pamir Moho at ～65 km depth and suggest an average thermal gradient of ～12–13 °C km?1. The relatively cold geotherm implies the introduction of these rocks to mantle depths by subduction or gravitational foundering (transient crustal drip). The xenoliths provide a window into a part of the orogenic history in which crustal material reached UHT–(U)HP conditions, partially melted, and then decompressed, without being overprinted by the later post‐thermal relaxation history.  相似文献   

14.
Dehydration melting of tonalites. Part II. Composition of melts and solids   总被引：6，自引：0，他引：6  
 Dehydration melting of tonalitic compositions (phlogopite or biotite-plagioclase-quartz assemblages) is investigated within a temperature range of 700–1000°C and pressure range of 2–15 kbar. The solid reaction products in the case of the phlogopite-plagioclase(An45)-quartz starting material are enstatite, clinopyroxene and potassium feldspar, with amphiboles occurring occasionally. At 12 kbar, zoisite is observed below 800°C, and garnet at 900°C. The reaction products of dehydration melting of the biotite (Ann50)-plagioclase (An45)-quartz assemblage are melt, orthopyroxene, clinopyroxene, amphibole and potassium feldspar. At pressures > 8 kbar and temperatures below 800°C, epidote is also formed. Almandine-rich garnet appears above 10 kbar at temperatures ≥ 750°C. The composition of melts is granitic to granodioritic, hence showing the importance of dehydration melting of tonalites for the formation of granitic melts and granulitic restites at pressure-temperature conditions within the continental crust. The melt compositions plot close to the cotectic line dividing the liquidus surfaces between quartz and potassium feldspar in the haplogranite system at 5 kbar and a H 2O = 1. The composition of the melts changes with the composition of the starting material, temperature and pressure. With increasing temperature, the melt becomes enriched in Al2O3 and FeO+MgO. Potash in the melt is highest just when biotite disappears. The amount of CaO decreases up to 900°C at 5 kbar whereas at higher temperatures it increases as amphibole, clinopyroxene and more An-component dissolve in the melt. The Na2O content of the melt increases slightly with increase in temperature. The composition of the melt at temperatures > 900°C approaches that of the starting assemblage. The melt fraction varies with composition and proportion of hydrous phases in the starting composition as well as temperature and pressure. With increasing modal biotite from 20 to 30 wt%, the melt proportion increases from 19.8 to 22.3 vol.% (850°C and 5 kbar). With increasing temperature from 800 to 950°C (at 5 kbar), the increase in melt fraction is from 11 to 25.8 vol.%. The effect of pressure on the melt fraction is observed to be relatively small and the melt proportion in the same assemblage decreases at 850°C from 19.8 vol.% at 5 kbar to 15.3 vol.% at 15 kbar. Selected experiments were reversed at 2 and 5 kbar to demonstrate that near equilibrium compositions were obtained in runs of longer duration. Received: 27 December 1995 / Accepted: 7 May 1996  相似文献   

15.
The Windmill Islands region in Wilkes Land, east Antarctica, preserves granulite facies metamorphic mineral assemblages that yield seemingly comparable P–T estimates from conventional thermobarometry and mineral equilibria modelling. This is uncommon in granulite facies terranes, where conventional thermobarometry and phase equilibria modelling generally produce conflicting P–T estimates because peak mineral compositions tend to be modified by retrograde diffusion processes. In situ U–Pb monazite geochronology and calculated metamorphic phase diagrams show that the Windmill Islands experienced two phases of high thermal gradient metamorphism during the Mesoproterozoic. The first phase of metamorphism is recorded by monazite ages in two widely separated samples and occurred at c. 1,305 Ma. This event was regional in extent, involved crustally derived magmatism and reached conditions of ~3.2–5 kbar and 690–770°C corresponding to very high thermal gradients of >150°C/kbar. The elevated thermal regime is interpreted to reflect a period of extension or increased extension in a back‐arc setting that existed prior to c. 1,330 Ma. The first metamorphic event was overprinted by granulite facies metamorphism at c. 1,180 Ma that was coeval with the intrusion of charnockite. This event involved peak temperatures of ~840–850°C and pressures of ~4–5 kbar. A phase of granitic magmatism at c. 1,250–1,210 Ma, prior to the intrusion of the charnockite, is interpreted to reflect a phase of compression within an overall back‐arc setting. Existing conventional thermobarometry suggests conditions of ~4 kbar and 750°C for M1 and 4–7 kbar and 750–900°C for M2. The apparent similarities between the phase equilibria modelling and existing conventional thermobarometry may suggest either that the terrane cooled relatively quickly, or that the P–T ranges obtained from conventional thermobarometry are sufficiently imprecise that they cover the range of P–T conditions obtained in this study. However, without phase equilibria modelling, the veracity of existing conventional P–T estimates cannot be evaluated. The calculated phase diagrams from this study allow the direct comparison of P–T conditions in the Windmill Islands with phase equilibria models from other regions in the Musgrave–Albany–Fraser–Wilkes Orogen. This shows that the metamorphic evolution of the Wilkes Land region is very similar to that of the eastern Albany–Fraser Orogen and Musgrave Province in Australia, and further demonstrates the remarkable consistency in the timing of metamorphism and the thermal gradients along the ~5,000 km strike length of this system.  相似文献   

16.
The high-grade metamorphic terrane in the Badu region along the northeastern Cathaysia Block in South China preserves retrograded eclogites and mafic granulites. Here we present the petrology, mineral phase equilibria and P-T conditions based on pseudosection computations, as well as zircon U-Pb ages of these rocks. Mineral textures and reaction relationships suggest four metamorphic stages for the retrograded eclogite as follows: (1) eclogite facies stage (M1), (2) clinopyroxene retrograde stage (M2), (3) amphibole retrograde stage (M3), and (4) chlorite retrograde stage (M4). For the mafic granulite, three stages are identified as: (1) plagioclase-absent stage (M1), (2) granulite facies stage (M2) and (3) amphibolite facies stage (M3). Metamorphic evolution of both of the rock types follows clockwise P-T path. Conventional geothermometers and geobarometers in combination with phase equilibria modelling yield metamorphic P-T conditions for each metamorphic stage for the eclogite as 500–560 °C, 23–24 kbar (M1), 640–660 °C, 14–16 kbar (M2), 730–750 °C, and 11–13 kbar (M3). The chlorite retrograde stage (M4) is inferred to have occurred at lower amphibolite to greenschist facies conditions. Phase equilibria modelling of the mafic granulite shows P-T conditions for each metamorphic stage as 600–720 °C, > 13 kbar (M1) and 860–890 °C, 5–6 kbar (M2) and M3 at amphibolite facies conditions. LA-ICPMS zircon U-Pb dating and trace element analysis show that the high pressure metamorphism occurred at 245–251 Ma. Protolith age of the mafic granulite is 997 Ma, similar to that of the mafic to ultramafic rocks widely distributed in the Cathaysia Block and also along the Jiangnan belt. Subduction of ancient oceanic lithospheric materials (or crustal thickening) during Mesozoic and formation of eclogites suggest that the Cathaysia Block was perhaps in the Tethyan oceanic domain at this time. The granulite formation might have been aided by Mesozoic mafic magma underplating associated with lithospheric delamination, heating and retrogression of the eclogite accompanied by rapid uplift.  相似文献   

17.
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, Xgrs is constant as Xpy rises, and in pattern II Xgrs decreases as Xpy 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.  相似文献   

18.
Tertiary volcanics in the northern zone of the Eastern Pontides are characterized by subaerial and shallow-subaqueous facieses, and are divided into three volcanic suites: Eocene aged (1) basalt-trachybasalt-basaltic trachyandesite (BTB) and (2) trachyte-trachyandesite (TT), and Miocene aged (3) basanite-tephrite (BT) suites. Clinopyroxene is a common phase in all three volcanic suites, and has different compositions with Mg# varying from 0.57 to 0.91 in BTB suite and 0.57–0.84 in TT suite to 0.65–0.90 in BT suite. Feldspars in all suites generally exhibit wide range of compositions from sanidine to albite or anorthite and have weak normal and reverse compositional zoning. Olivines in BTB and BT suites have Fo60–92. Hornblendes in BTB, TT and BT suites are commonly magnesio-hastingsite and rare pargasite in composition (Mg#: 0.67–0.90). Brown mica is mainly phlogopite with Mg# ranging from 0.56 to 0.92 in the BTB suite, 0.59–0.84 in the TT suite, and 0.75–0.93 in the BT suite. Analcime is present only in the BT suite rocks. Fe–Ti oxides in all suites are mainly composed of magnetite and titanomagnetite. Textural petrographic and mineral chemical data suggest that magmas had undergone hydrous and anhydrous crystallizations in deep-, mid-, and shallow-crustal magma chambers. Clinopyroxene thermobarometric calculations show that Eocene magma chambers were characterized by temperature ranging from 1,100 to 1,244 °C and pressure ranging from 1.84 to 5.39 kbar. Similarly, the Miocene magma chambers were characterized by temperature ranging from 1,119 to 1,146 °C and pressure ranging from 4.23 to 4.93 kbar. Hornblende thermobarometry, oxygen fugacity, and hygrometer reveal that the crystallization temperature of Eocene volcanics range from 956 to 959 °C at pressure ranging from 6.49 to 6.52 kbar. Eocene volcanics were characterized by water content ranging from 7.83 to 8.57 wt.% and oxygen fugacity of 10?9.36 to 10?9.46 (ΔNNO+2). Miocene volcanics had crystallization temperature ranging from 970 to 978 °C at pressure ranging from 8.70 to 9.00 kbar with water content ranging from 8.04 to 8.64 wt.% and oxygen fugacity ranging from 10?8.75 to 10?8.87 (ΔNNO+2). Brown mica thermobarometric data show that Eocene volcanics were characterized by relatively high oxygen fugacity varying from 10-10.32 to 10-12.37 (HM) at temperature ranging from 858 to 953 °C and pressure ranging from 1.08 to 1.41 kbar. Miocene volcanics were crystallized at highly oxidized conditions, which are characterized by high oxygen fugacity of 10?12.0 (HM) at temperature of 875 °C and pressure of 2.09 kbar. The wide range of obtained temperatures for clinopyroxenes of the suites denotes that the equilibration of clinopyroxene crystals initiates from depth until close to the surface before magma eruption. The compositional variations, resorbed core and reverse zoning patterns in clinopyroxene phenocrysts, as well as variable pressures of crystallization, further indicate that the magmas that formed the suites were polybaric in origins and were composite products of more than one petrogenetic stage. The observed range of phenocryst assemblage and different compositional trends possibly originated from fractionation of magmas with different initial water contents under variable pressures of crystallization. The repeated occurrence of magmas from different suites during a single period of activity suggests that the magmatic system consists of several conduit systems and that magma reservoirs are dispersed at different levels of crustal magma chambers.  相似文献   

19.
The polymorphic relations for Mg3(PO4)2 and Mg2PO4OH have been determined by reversed experiments in the temperature-pressure (T-P) range 500–1100 °C, 2–30 kbar. The phase transition between the low-pressure phase farringtonite and Mg3(PO4)2-II, the Mg analogue of sarcopside, is very pressure dependent and was tightly bracketed between 625 °C, 7 kbar and 850 °C, 9 kbar. The high-temperature, high-pressure polymorph, Mg3(PO4)2-III, is stable above 1050 °C at 10 kbar and above 900 °C at 30 kbar. The low-pressure stability of farringtonite is in keeping with its occurrence in meteorites. The presence of iron stabilizes the sarcopside-type phase towards lower P. From the five Mg2PO4OH polymorphs only althausite, holtedahlite, β-Mg2PO4OH (the hydroxyl analogue of wagnerite) and ɛ-Mg2PO4OH were encountered. Relatively speaking, holtedahlite is the low-temperature phase (<600 °C), ɛ-Mg2PO4OH the high-temperature, low-pressure phase and β-Mg2PO4OH the high-temperature, high-pressure phase, with an intervening stability field for althausite which extends from about 3 kbar at 500 °C to about 12 kbar at 800 °C. Althausite and holtedahlite are to be expected in F-free natural systems under most geological conditions; however, wagnerite is the most common Mg-phosphate mineral, implying that fluorine has a major effect in stabilizing the wagnerite structure. Coexisting althausite and holtedahlite from Modum, S. Norway, show that minor fluorine is strongly partitioned into althausite (KD F/OH≈ 4) and that holtedahlite may incorporate up to 4 wt% SiO2. Synthetic phosphoellenbergerite has a composition close to (Mg0.9□0.1)2Mg12P8O38H8.4. It is a high-pressure phase, which breaks down to Mg2PO4OH + Mg3(PO4)2 + H2O below 8.5 kbar at 650 °C, 22.5 kbar at 900 °C and 30 kbar at 975 °C. The stability field of the phosphate end-member of the ellenbergerite series extends therefore to much lower P and higher T than that of the silicate end-members (stable above 27 kbar and below ca. 725 °C). Thus the Si/P ratio of intermediate members of the series has a great barometric potential, especially in the Si-buffering assemblage with clinochlore + talc + kyanite + rutile + H2O. Application to zoned ellenbergerite crystals included in the Dora-Maira pyrope megablasts, western Alps, reveals that growth zoning is preserved at T as high as 700–725 °C. However, the record of attainment of the highest T and/or of decreasing P through P-rich rims (1 to 2 Si pfu) is only possible in the presence of an additional phosphate phase (OH-bearing or even OH-dominant wagnerite in these rocks), otherwise the trace amounts of P in the system remain sequestered in the core of Si-rich crystals (5 to 8 Si pfu) and can no longer react. Received: 7 April 1995 / Accepted: 12 November 1997  相似文献   

20.
Sixty-three internally consistent geothermobarometers for mineral equilibria involving sapphirine (2:2:1 and 7:9:3), pyrope, cordierite, enstatite, Mg-tschermak orthopyroxene, quartz, spinel and sillimanite have been calibrated in the MAS system. The updated thermodynamic data of these minerals are consistent, within limits of error, with highP-T experiments on several mineral equilibria and calorimetric data. TheP-T conditions of the granulite facies metamorphism, spanning a range of 700 to more than 1000°C and 4 to more than 10 kbar, can be estimated simultaneously from these geothermobarometers andP-T-t trajectories can be deduced from the reaction coronas well preserved in these rocks because of the refractory nature of aluminous phases. The geothermobarometers have been applied to sapphirine-spinel granulites of Eastern Ghats and Enderby Land. TheP-T conditions of metamorphism (a-prograde/thermal peak and b-retrograde isothermal/isobaric decompression/cooling) estimated for these granulites are: (1) Eastern Ghats (Visakhapatnam): Paderu- (a) 900°C/8.3kbar, (b-1) 900°C/6.8kbar and (b-2) 740°C/5.4 kbar; Anantgiri- (a) prograde anticlockwise 930°C/6.2 kbar and (b) 870°C/6.8 kbar, 820°C/6.1 kbar; Anakapalle- (b) 845°C/8.5-6.2 kbar; and Araku- (b) 840°C/6.2 kbar to 795°C/5.9 kbar. Enderby Land (Napier complex): Spot height 945, Tula Mts.- (a) 970°C/9.1 ± 0.6 kbar, isobaric cooling (b) 885°C/ 7.75 kbar, isothermal decompression (b) 880°C/6.85 kbar; Mt. Hardy, Tula Mts.- (b) 885°C/6.75 kbar; Mt. Riiser-Larsen, Amundsen bay- (a) 1000°C/7.0 kbar prograde anticlockwise; Mt. Sones- (b) 920°C/ 6.8 kbar; Forefinger Point, SW Enderby Land- (b) 840°C/6.7 kbar, 810°C/6.5 kbar and 775°C/5.0 kbar. The estimatedP-T andP-T-t are mostly consistent with those inferred from the granulites of these areas.  相似文献   

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