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1.
Regularly oriented orthopyroxene (opx) and forsterite (fo) inclusions occur as opx + rutile (rt) or fo + rt inclusion domains in garnet (grt) from Otrøy peridotite. Electron diffraction characterization shows that forsterite inclusions do not have any specific crystallographic orientation relationships (COR) with the garnet host. In contrast, orthopyroxene inclusions have two sets of COR, that is, COR‐I: <111>grt//<001>opx and {110}grt～//～{100}opx (～13° off) and COR‐II: <111>grt//<011>opx and {110}grt～//～{100}opx (～14° off), in four garnet grains analysed. Both variants of orthopyroxene have a blade‐like habit with one pair of broad crystal faces parallel/sub‐parallel to {110}grt plane and the long axis of the crystal, <001>opx for COR‐I and <011>opx for COR‐II, along <111>grt direction. Whereas the lack of specific COR between forsterite and garnet, along with the presence of abundant infiltrating trails/veinlets decorated by fo + rt at garnet edges, provide compelling evidence for the formation of forsterite inclusions in garnet through the sequential cleaving–infiltrating–precipitating–healing process at low temperatures, the origin of the epitaxial orthopyroxene inclusions in garnet is not so obvious. In this connection, the reported COR, the crystal habit and the crystal growth energetics of the exsolved orthopyroxene in relict majoritic garnet were reviewed/clarified. The exsolved orthopyroxene in a relict majoritic garnet follows COR‐III: {112}grt//{100}opx and <111>grt//<001>opx. Based on the detailed trace analysis on published SEM images, these exsolved orthopyroxene inclusions are shown to have the crystal habit with one pair of broad crystal faces parallel to {112}grt//{100}opx and the long crystal axis along <111>grt//<001>opx. Such a crystal habit can be rationalized by the differences in oxygen sub‐lattices of both structures and represents the energetically favoured crystal shape of orthopyroxene inclusions in garnet formed by solid‐state exsolution mechanism. Considering the very different COR, crystal habit, as well as crystal growth direction, the orthopyroxene inclusions in garnet of the present sample most likely had been formed by mechanism(s) other than solid‐state exsolution, regardless of their regularly oriented appearance in garnet and the COR specification between orthopyroxene and garnet. In fact, the crystallographic characteristics of orthopyroxene and the similar chemical compositions of garnet at opx + rt inclusion domains, fo + rt inclusion domains/trails and garnet rim suggest that the orthopyroxene inclusions in the garnet are most likely formed by similar cleaving‐infiltration process as forsterite inclusions, though probably at an earlier stage of metamorphism. This work demonstrates that the oriented inclusions in host minerals, with or without specific COR, can arise from mechanism(s) other than solid‐state exsolution. Caution is thus needed in the interpretation of such COR, so that an erroneous identification of exhumation from UHP depths would not be made.  相似文献   

2.
The asterism effect of star garnet has been attributed to the oriented distribution of needle‐like rutile inclusions. Rutile needles occur in garnet from a wide range of metamorphic settings and rock bulk compositions, and their origin has been ascribed to different mechanisms, such as exsolution, and used to interpret petrological and tectonic processes. Results from an optical and transmission electron microscopy of Idaho star garnet indicate a co‐precipitation origin. It was found that rutile needles are predominantly oriented along the <103>rt//<111>grt and <001>rt//<001>grt directions following multiple crystallographic orientation relationships (CORs); i.e. COR‐1, 2, 2′, 3, 4 and 5 in 6‐ray star garnet, and are oriented solely along the <103>rt//<111>grt directions following exclusively COR‐2 in 4‐ray star garnet. The sole presence of COR‐2 <111>grt needles in the common 4‐ray star garnet, in contrast to the presence of both <111>grt and <001>grt needles with multiple CORs in the rare 6‐ray star garnet, suggests that the COR‐2 <111>grt needle probably is the energetically most favoured variant, as is also supported by the coincidence site lattice considerations. The unique crystallography‐controlled microstructures of 4‐ray star garnet, including the cloudy domains behind the {111}grt or {100}grt fronts with abundant inclusions of rutile needle, rutile compound needle and multiple‐phase‐inclusion, as well as the clear domains behind the {110}grt fronts with only a few above inclusions concentrated exclusively within the linear, <110>grt‐oriented, continuous tube‐like domains, further suggest that the COR‐2 <111>grt needles in 4‐ray star garnet most likely have a growth‐in origin, co‐precipitating with garnet at its growth fronts close to thermodynamic equilibrium conditions. The 6‐ray star garnet, on the other hand, most likely formed under far‐from equilibrium conditions, thereby yielding a maximum of 99 crystallographic variants of rutile needles with multiple CORs in a single crystal. In the light of these findings, along with the common occurrences of the sole COR in many inclusion‐host systems owing to the requirement to minimize the energy barrier in an exsolution process, the presence of both <103>rt//<111>grt and <001>rt//<001>grt needles with multiple CORs in garnet of Sulu eclogite and Erzegebirge quartzofeldspathic rock would therefore cast doubt on the assertion of an exsolution origin of rutile needles in garnet from these ultrahigh‐pressure rocks.  相似文献   

3.
Metamorphic garnet commonly contains needle‐like rutile inclusions as well as equant rutile inclusions that surround quartz inclusions and range in size from submicrometer to nanometer. Although the origin of these equant rutile inclusions, that is, exsolution or non‐exsolution, has important implications for petrological and tectonic processes, the crystallographic characteristics of these inclusions have rarely been studied because of the small sizes and analytical difficulties involved. Here, we report the crystallographic characteristics pertinent to the genetic origin of minute equant rutile inclusions in cloudy, nearly spherically shaped garnet domains with Ti‐depleted compositions surrounding quartz inclusions in ultrahigh‐pressure garnet from several diamondiferous Erzgebirge quartzofeldspathic gneissic rock samples. TEM analyses show that the equant rutile crystals in cloudy garnet domains are partially bounded by the low‐energy {100}rt ± {110}rt ± {101}rt facets and have rather random crystallographic orientation relationships (CORs) with the garnet host, with preferential alignment of low‐energy lattice planes, for example, {100}rt//{112}grt, for some rutile crystals. Although the rather random CORs are unlikely to be attributed to solid‐state exsolution subjected to the stringent topotactic garnet lattice constraints, the characteristic subhedral {100}rt ± {110}rt ± {101}rt crystal forms of rutile can be rationalized by a metasomatic dissolution‐reprecipitation mechanism via a fluid phase. In this scenario, the quartz+fluid inclusions in garnet were first subjected to decompression microcracking during rock exhumation, followed by dissolution of Ti‐bearing garnet matrix at the crack tips or along the crack surfaces and subsequent reprecipitation of rutile, apatite, gahnite, akdalaite, and Ti‐depleted garnet. The rapid coalescence between rutile and garnet crystals in fluid or direct attachment of rutile crystals onto the dissolving crack surfaces would then yield the rather random CORs as reported here. These results, along with previous work on rutile needles, indicate rather diverse genesis of rutile inclusions in various crystal forms, thus shedding light on the controversial exsolution origin for other inclusion suite/microstructure in minerals.  相似文献   

4.
Optical microscopy, secondary electron microscopy and analytical electron microscopy were used to characterize crystallographic orientation relationships between oriented mineral inclusions and clinopyroxene (Cpx) host from the Hujialing garnet clinopyroxenite within the Sulu ultrahigh-pressure (UHP) terrane, eastern China. One garnet clinopyroxenite sample (2HJ-2C) and one megacrystic garnet-bearing garnet clinopyroxenite (RZ-11D) were studied. Porphyroblastic clinopyroxene from sample 2HJ-2C contains oriented inclusions of ilmenite (Ilm), spinel (Spl), magnetite and garnet, whereas clinopyroxene inclusions within megacrystic garnet from sample RZ-11D contain oriented inclusions of ilmenite and amphibole. Specific crystallographic relationships were observed between ilmenite/spinel plates and host clinopyroxene in sample 2HJ-2C and between ilmenite plates and host clinopyroxene in sample RZ-11D, i.e. [1[`1]00 1\bar{1}00 ]Ilm//[0[`1]0 0\bar{1}0 ]Cpx (0001)Ilm//(100)Cpx; and [110]Spl//[0[`1]0 0\bar{1}0 ]Cpx ([`1]11 \bar{1}11 )Spl//(100)Cpx. These inclusions are suggested to be primary precipitates via solid-state exsolutions. Most of the needle-like magnetite/spinel inclusions generally occur at the rims or along fractures of clinopyroxene within sample 2HJ-2C. Despite the epitaxial relation with host clinopyroxene, these magnetite/spinel needles would have resulted from fluid/melt infiltrations. Non-epitaxial garnet lamellae in clinopyroxene of sample 2HJ-2C were formed via fluid infiltration-deposition primarily along (010) and subordinately along (100) partings. Epitaxial amphibole plates (with a thickness <1 μm) and lamellae (with a thickness = 1–10 μm) in host clinopyroxene of sample RZ-11D were probably results of hydration processes, although amphibole plates could otherwise be interpreted as exsolution products. Temporal relations between mineral inclusions in each sample can be established, and a semi-quantitative P–T path for this garnet clinopyroxenite body was derived accordingly. The present results show that the Hujialing garnet clinopyroxenite may not have subducted to mantle depths as deep as 250 km during UHP metamorphism as suggested by previous studies. This study demonstrates that the crystallographic and temporal/spatial relationships between aligned inclusions and host minerals are essential to a correct genetic interpretation of metamorphic rocks.  相似文献   

5.
Garnet growth in high‐pressure, mafic garnet granulites formed by dehydration melting of hornblende‐gabbronorite protoliths in the Jijal complex (Kohistan palaeo‐island arc complex, north Pakistan) was investigated through a microstructural EBSD‐SEM and HRTEM study. Composite samples preserve a sharp transition in which the low‐pressure precursor is replaced by garnet through a millimetre‐sized reaction front. A magmatic foliation in the gabbronorite is defined by mafic‐rich layering, with an associated magmatic lineation defined by the shape‐preferred orientation (SPO) of mafic clusters composed of orthopyroxene (Opx), clinopyroxene (Cpx), amphibole (Amp) and oxides. The shape of the reaction front is convoluted and oblique to the magmatic layering. Opx, Amp and, to a lesser extent, Cpx show a strong lattice‐preferred orientation (LPO) characterized by an alignment of [001] axes parallel to the magmatic lineation in the precursor hornblende‐gabbronorite. Product garnet (Grt) also displays a strong LPO. Two of the four 〈111〉 axes are within the magmatic foliation plane and the density maximum is subparallel to the precursor magmatic lineation. The crystallographic relationship 〈111〉Grt // [001]Opx,Cpx,Amp deduced from the LPO was confirmed by TEM observations. The sharp and discontinuous modal and compositional variations observed at the reaction front attest to the kinetic inhibition of prograde solid‐state reactions predicted by equilibrium‐phase diagrams. The P–T field for the equilibration of Jijal garnet granulites shows that the reaction affinities are 5–10 kJ mol.?1 for the Grt‐in reaction and 0–5 kJ mol.?1 for the Opx‐out reaction. Petrographic and textural observations indicate that garnet first nucleated on amphibole at the rims of mafic clusters; this topotactic replacement resulted in a strong LPO of garnet. Once the amphibole was consumed in the reaction, the parallelism of [001] axes of the mafic‐phase reactants favoured the growth of garnet crystals with similar orientations over a pyroxene substrate. These aggregates eventually sintered into single‐crystal garnet. In the absence of deformation, the orientation of mafic precursor phases conditioned the nucleation site and the crystallographic orientation of garnet because of topotaxial transformation reactions and homoepitaxial growth of garnet during the formation of high‐pressure, mafic garnet‐granulite after low‐pressure mafic protoliths.  相似文献   

6.
We report here the detailed microstructure and chemistry of pyroxene exsolution from a polycrystalline garnet porphyroblast of the Western Gneiss Region (WGR) garnet peridotite, Otrøy, Norway. For both clinopyroxene (Cpx) and orthopyroxene (Opx), the same basic crystallographic relationship is found with the host garnet: (100)py//{112}grt, (010)px//{110}grt and (001)px//{111}grt for the majority (>90%) of its intracrystalline pyroxene rods. In addition, this pattern is also exhibited by some interstitial Opx and a subpopulation of both pyroxenes shows a different pattern or no discernible pattern. The results provide quantitative microstructural evidence demonstrating an exsolution (precipitation) origin of both the intracrystalline Cpx and Opx and the small interstitial Opx crystals. The reconstructed precursor majoritic garnet, taking into account both the intracrystalline pyroxenes and interstitial Opx, was characterized by Si = ～3.07 cation per formula unit that corresponds to a minimum pressure of 7.7 GPa (～250 km depth). We also deduce from the observation of Opx being the majority of intracrystalline precipitates and 100% of the interstitial ones that the precursor majoritic garnet probably originated from a pressure less than ～10 GPa (～300 km depth). A multistage decomposition hypothesis is proposed for this WGR majoritic garnet during exhumation of the peridotite from 250 to 300 km depth to explain the topotaxy and chemistry of the exsolved pyroxenes.  相似文献   

7.
Multiple regression analysis on an extended dataset has been performed to refine the relationship between temperature, pressure, composition and the Fe–Mg distribution between garnet and clinopyroxene. In addition to a significant dependence between the distribution coefficient KD and X GrtCa and X GrtMg#, as shown by the experimental data, the effect of X GrtMn has also been incorporated using data from natural Mn‐rich garnet–clinopyroxene pairs. Multiple regression of data (n=360) covering a large span in pressure, temperature and composition from 27 experimental datasets, combined with 49 natural high‐Mn granulites from Ruby Range, Montana, USA, and Karnataka, India, yields the P–T –compositional relationship (r2=0.98): where KD=(Fe2+/Mg)Grt/(Fe2+/Mg)Cpx, X GrtCa=Ca/(Ca+Mn+Fe2++Mg) in garnet, X GrtMn= Mn/(Ca+Mn+Fe2++Mg) in garnet, and X GrtMg#=Mg/(Mg+Fe2+) in garnet. The Fe2+–Mg equilibrium between garnet and clinopyroxene does not seem to be affected by variations in the sodic content of the co‐existing clinopyroxene in the range X CpxNa=0–0.51. Comparisons between the new and former calibrations of the garnet–clinopyroxene Fe2+–Mg geothermometer clearly demonstrate how the various parameters in each case affect the calculated temperatures. Application of the new expression gives reasonable results for natural garnet–clinopyroxene pairs from various rock types and settings, and should be preferred to previous formulations. Using the new calibration to the self‐consistent dataset of Pattison & Newton (Contributions to Mineralogy and Petrology, 1989, 101, 87–103) suggests a systematic deviation with regard to both temperature and composition between their dataset and the datasets used in the present calibration.  相似文献   

8.
On the origin of oriented rutile needles in garnet from UHP eclogites   总被引：4，自引：0，他引：4  
Although oriented rutile needles in garnet have been reported from several ultrahigh‐pressure (UHP) rocks and considered to be important UHP indicators, their crystallographic features including growth habit and lattice correspondences with garnet host have never been properly characterized. This paper presents a detailed analytical electron microscopic (AEM) study on evenly distributed oriented rutile needles in garnet of two eclogitic rocks from Sulu. Some garnet in one UHP diamondiferous quartzofeldspathic rock from the Saxonian Erzgebirge, and in one high‐pressure (HP) felsic granulite from Bohemia also contain a few unevenly distributed oriented rutile needles. They have also been studied for the purpose of comparison. Despite different distribution patterns, AEM revealed that all rutile needles are oriented along the 〈111〉 directions of garnet with their lateral sides surrounded by the {110} planes of garnet, and that the growth directions of most needles are close to the normal of the {101} planes of rutile. No other specific crystallographic orientation relationships between rutile and garnet host were observed, and there is no pyroxene associated with rutile, as necessitated by the precipitation reaction of rutile in garnet as previously proposed. A simple solid‐state precipitation scenario for the formation of the rutile needles in garnet in these two eclogitic rocks is not justified. Three alternative mechanisms are considered for the formation of oriented rutile needles: (i) the rutile needles may be inherited from precursor minerals; (ii) the rutile needles may be formed by a dissolution–reprecipitation mechanism; and (iii) the rutile needles may be formed by cleaving and healing of garnet with rutile deposition. None of these mechanisms can fully explain the observations, although the first one is less likely and the third one is preferred. This study presents an example where the presence of oriented/aligned inclusions in minerals does not necessarily imply a precipitation origin.  相似文献   

9.
A combined oxygen‐isotope and fluid‐inclusion study has been carried out on high‐ and ultrahigh‐pressure metamorphic (HP/UHPM) eclogites and garnet clinopyroxenite from the Dabie‐Sulu terranes in eastern China. Coesite‐bearing eclogites/garnet clinopyroxenite and quartz eclogites have a wide range in whole‐rock δ18OVSMOW, from 0 to 11‰. The high‐T oxygen‐isotope fractionations preserved between quartz and garnet preclude significant retrograde isotope exchange during exhumation, and the wide range in whole‐rock oxygen‐isotope composition is thought to be a presubduction signature of the precursors. Aqueous fluids with variable salinities and gas species (N2‐, CO2‐, or CH4‐rich), are trapped as primary inclusions in garnet, omphacite and epidote, and in quartz blebs enclosed within eclogitic minerals. In high‐δ18O HP/UHPM rocks from Hujialin and Shima, high‐salinity brine and/or N2 inclusions occur in garnet porphyroblasts, which also contain inclusions of coesite, Cl‐rich blue amphibole and dolomite. In contrast, in low‐δ18O eclogites from Qinglongshan and Huangzhen, the Cl concentrations in amphibole are very low, < 0.2 wt.%, and low‐salinity aqueous inclusions occur in quartz inclusions in epidote porphyroblasts and in epidote cores. These low‐salinity fluid inclusions are believed to be remnants of meteoric water, although the fluid composition was modified during pre‐ and syn‐peak HP/UHPM. Eclogites at Houshuichegou and Hetang contain CH4‐rich fluid inclusions, coexisting with high‐salinity brine inclusions. Methane was probably formed under the influence of CO2‐rich aqueous fluids during serpentinisation of mantle‐derived peridotites prior to or during plate subduction. Remnants of premetamorphic low‐ to high‐salinity aqueous fluid with minor N2 and/or other gas species preserved in the Dabie‐Sulu HP/UHPM eclogites and garnet clinopyroxenite indicate a great diversity of initial fluid composition in the precursors, implying very limited fluid–rock interaction during syn‐ and post‐peak HP/UHPM.  相似文献   

10.
王汝成  王硕  邱检生  倪培 《岩石学报》2009,25(7):1603-1611
石榴子石是榴辉岩中的基本造岩矿物。本文对苏鲁地体中的毛北榴辉岩和大别地体中的双河榴辉岩中的石榴子石进行了研究。结果显示,石榴子石都表现出中心“富”钛特征,即石榴子石颗粒的中心部位的TiO2含量（0.10%~0.50%）明显高于正常榴辉岩中石榴子石的钛含量(TiO2 一般<0.1%)。另外,在石榴子石中心部位含有大量金红石及其它钛矿物包裹体,其定向分布特征揭示其出溶成因模式。计算结果显示,出溶金红石的原始石榴子石大约含1.7% TiO2,揭示其超深源特征。此外,在石榴子石中发现了一颗TiO2含量达8%~9%的钙铝榴石,具超深源成因特征。因此,本文认为超钛钙铝榴石也是超高压变质作用的标志矿物。  相似文献   

11.
Garnet granulite facies mid‐to lower crust in Fiordland, New Zealand, provides evidence for pulsed intrusion and deformation occurring in the mid‐to lower crust of magmatic arcs. 238U‐206Pb zircon ages constrain emplacement of the ～595 km2 Malaspina Pluton to 116–114 Ma. Nine Sm‐Nd garnet ages (multi‐point garnet‐rock isochrons) ranging from 115.6 ± 2.6 to 110.6 ± 2.0 Ma indicate that garnet granulite facies metamorphism was synchronous or near synchronous throughout the pluton. Hence, partial melting and garnet granulite facies metamorphism lasted <5 Ma and began within 5 Ma of pluton emplacement. Garnet granulite facies L‐S tectonites in the eastern part of the Malaspina Pluton record the onset of extensional strain and arc collapse. An Sm‐Nd garnet age and thermobarometric results for these rocks directly below the amphibolite facies Doubtful Sound shear zone provide the oldest known age for extension in Fiordland at ≥112.8 ± 2.2 Ma at ～920 °C and 14–15 kbar. Narrow high Ca rims in garnet from some of these suprasolidus rocks could reflect a ≤ 1.5 kbar pressure increase, but may be largely a result of temperature decrease based on the Ca content of garnet predicted from pseudosections. At peak metamorphic conditions >900 °C, garnet contained ～4000 ppm Ti; subsequently, rutile inclusions grew during declining temperature with limited pressure change. Garnet granulite metamorphism of the Malaspina Pluton is c. 10 Ma younger than similar metamorphism of the Pembroke Granulite in northern Fiordland; therefore, high‐P metamorphism and partial melting must have been diachronous for this >3000 km² area of mid‐to‐lower crust. Thus, two or more pulses of intrusion shortly followed by garnet granulite metamorphism and extensional strain occurred from north to south along the axis of the lower crustal root of the Cretaceous Gondwana arc.  相似文献   

12.
Published experimental data including garnet and clinopyroxene as run products were used to develop a new formulation of the garnet–clinopyroxene geothermometer based on 333 garnet–clinopyroxene pairs. Only experiments with graphite capsules were selected because of difficulty in estimating the Fe3+ content of clinopyroxene. For the calibration, a published subregular‐solution model was adopted to express the non‐ideality of garnet. The magnitude of the Fe–Mg excess interaction parameter for clinopyroxene (WFeMgCpx), and differences in enthalpy and entropy of the Fe–Mg exchange reaction were regressed from the accumulated experimental data set. As a result, a markedly negative value was obtained for the Fe–Mg excess interaction parameter of clinopyroxene (WFeMgCpx = ? 3843 J mol?1). The pressure correction is simply treated as linear, and the difference in volume of the Fe–Mg exchange reaction was calculated from a published thermodynamic data set and fixed to be ?120.72 (J kbar?1 mol?1). The regressed and obtained thermometer formulation is as follows: where T = temperature, P = pressure (kbar), A = 0.5 Xgrs (Xprp ? Xalm ? Xsps), B = 0.5 Xgrs (Xprp ? Xalm + Xsps), C = 0.5 (Xgrs + Xsps) (Xprp ? Xalm), Xprp = Mg/(Fe2+ + Mn + Mg + Ca)Grt, Xalm = Fe/(Fe2+ + Mn + Mg + Ca)Grt, Xsps = Mn/(Fe2+ + Mn + Mg + Ca)Grt, Xgrs = Ca/(Fe2+ + Mn + Mg + Ca)Grt, XMgCpx = Mg/(Al + Fetotal + Mg)Cpx, XFeCpx = Fe2+/(Al + Fetotal + Mg)Cpx, KD = (Fe2+/Mg)Grt/(Fe2+/Mg)Cpx, Grt = garnet, Cpx = clinopyroxene. A test of this new formulation to the accumulated data gave results that are concordant with the experimental temperatures over the whole range of the experimental temperatures (800–1820 °C), with a standard deviation (1 sigma) of 74 °C. Previous formulations of the thermometer are inconsistent with the accumulated data set; they underestimate temperatures by about 100 °C at >1300 °C and overestimate by 100–200 °C at <1300 °C. In addition, they tend to overestimate temperatures for high‐Ca garnet (Xgrs ≈ 0.30–0.50). This new formulation has been tested against previous formulations of the thermometer by application to natural eclogites. This gave temperatures some 20–100 °C lower than previous formulations.  相似文献   

13.
Coexisting garnet blueschist and eclogite from the Chinese South Tianshan high‐pressure (HP)–ultrahigh‐pressure (UHP) belt consist of similar mineral assemblages involving garnet, omphacite, glaucophane, epidote, phengite, rutile/sphene, quartz and hornblendic amphibole with or without paragonite. Eclogite assemblages generally contain omphacite >50 vol.% and a small amount of glaucophane (<5 vol.%), whereas blueschist assemblages have glaucophane over 30 vol.% with a small amount of omphacite which is even absent in the matrix. The coexisting blueschist and eclogite show dramatic differences in the bulk‐rock compositions with higher X(CaO) [=CaO/(CaO + MgO + FeOtotal + MnO + Na2O)] (0.33–0.48) and lower A/CNK [=Al2O3/(CaO + Na2O + K2O)] (0.35–0.56) in eclogite, but with lower X(CaO) (0.09–0.30) and higher A/CNK (0.65–1.28) in garnet blueschist. Garnet in both types of rocks has similar compositions and exhibits core–rim zoning with increasing grossular and pyrope contents. Petrographic observations and phase equilibria modelling with pseudosections calculated using thermocalc in the NCKMnFMASHO system for the coexisting garnet blueschist and eclogite samples suggest that the two rock types share similar P–T evolutional histories involving a decompression with heating from the Pmax to the Tmax stage and a post‐Tmax decompression with slightly cooling stage, and similar P–T conditions at the Tmax stage. The post‐Tmax decompression is responsible for lawsonite decomposition, which results in epidote growth, glaucophane increase and omphacite decrease in the blueschist, or in an overprinting of the eclogitic assemblage by a blueschist assemblage. Calculated P–X(CaO), P–A/CNK and P–X(CO2) pseudosections indicate that blueschist assemblages are favoured in rocks with lower X(CaO) (<0.28) and higher A/CNK (>0.75) or fluid composition with higher X(CO2) (>0.15), but eclogite assemblages preferentially occur in rocks with higher X(CaO) and lower A/CNK or fluid composition with lower X(CO2). Moreover, phase modelling suggests that the coexistence of blueschist and eclogite depends substantially on P–T conditions, which would commonly occur in medium temperatures of 500–590 °C under pressures of ~17–22 kbar. The modelling results are in good accordance with the measured bulk‐rock compositions and modelled temperature results of the coexisting garnet blueschist and eclogite from the South Tianshan HP–UHP belt.  相似文献   

14.
Corundum-rich garnetite occurs as an isolated lens in a garnet peridotite body in the Donghai area of the Sulu ultrahigh-pressure (UHP) terrane. This rock consists of garnet and corundum, along with minor crack-related zoisite, pargasite, Mg-staurolite, Mg-chloritoid, sapphirine and chlorite. Pyropic garnet (Prp54–63Grs26–36Alm10–12) exhibits a sinusoidal REE pattern, positive Ta, Pb, and negative Nb, Ti anomalies due to metasomatism. Reddish corundum contains 1.1–1.7 wt% Cr2O3, and shows three oriented sets of exsolved rutile needles. Both garnet and corundum contain inclusions of apatite, Mg-allanite (MgO>4 wt%), and Ni-Fe sulfides formed as trapped Ni-Fe-S melt. The protolith of the corundum-rich garnetite could have been spinel websterite formed in the upper mantle. Both the websterite and the host garnet peridotite were subjected to subduction-zone UHP metamorphism at 800 °C and >4 GPa. Crack-related hydrous phases were formed by fluid infiltration during exhumation.Editorial responsibility: T.L. Grove  相似文献   

15.
Omphacite and garnet coronas around amphibole occur in amphibolites in the Hong'an area, western Dabie Mountains, China. These amphibolites consist of an epidote–amphibolite facies assemblage of amphibole, garnet, albite, clinozoisite, paragonite, ilmenite and quartz, which is incompletely overprinted by an eclogite facies assemblage of garnet, omphacite and rutile. Coronas around amphibole can be divided into three types: an omphacite corona; a garnet–omphacite–rutile corona; and, a garnet–omphacite corona with less rutile. Chemographic analysis for local reaction domains in combination with petrographical observations show that reactions Amp + Ab + Pg = Omp +Czo + Qtz + H2O, and Amp + Ab = Omp ± Czo + Qtz + H2O may lead to the development of omphacite coronas. The garnet–omphacite–rutile corona was formed from the reaction Amp + Ab + Czo + Ilm ± Qtz = Omp + Grt + Rt + H2O. In garnet–omphacite coronas, the garnet corona grew during an early stage of epidote amphibolite facies metamorphism, whereas omphacite probably formed by the reactions forming the omphacite corona during the eclogite facies stage. It is estimated that these reactions occurred at 0.8–1.4 GPa and 480–610 °C using the garnet–clinopyroxene thermometer and omphacite barometer in the presence of albite.  相似文献   

16.
The discovery of eclogites is reported within the Great Himalayan Crystalline Complex in the Thongmön area, central Himalaya, and their metamorphic evolution is deciphered by petrographic studies, pseudosection modelling, and zircon dating. For the first time, omphacite has been found in the matrix of eclogites taken from a metamorphic mafic lens. Two groups of garnet have been identified in the Thongmön eclogites on the basis of major and rare earth elements and mineral inclusions. Core and intermediate sections of garnet represent Grt I, in which the major elements (Ca, Mg, and Fe) show a nearly homogenous distribution with little or weak zonation. This Grt I displays an almost flat chondrite‐normalized HREE pattern, and the main inclusions are amphibole, apatite, quartz, and abundant omphacite. Grt II, forms thin rims on large garnet grains, and is characterized by rim‐ward Ca decrease and Mg increase and MREE enrichment relative to HREE and LREE. No amphibole inclusions are found in Grt II, indicating the decomposition of amphibole contributed to its MREE enrichment. Two metamorphic stages, recorded by matrix minerals and inclusions in garnet and zircon, outline the burial of the Thongmön eclogites and progressive metamorphic processes to the pressure peak: (a) the assemblage of amphibole–garnet–omphacite–phengite–rutile–quartz, with the phengite interpreted as having been replaced by Bt+Pl symplectites, represents the prograde amphibole eclogite facies stage M1(1), (b) in the peak eclogite facies [stage M1(2)], amphibole was lost and melting started. Based on the compositions of garnet and omphacite inclusions, M1(1) is constrained to 19–20 kbar and 640–660°C and M1(2) occurred at >21 kbar, >750°C, with appearance of melt and its entrapment in metamorphic zircon. SHRIMP U–Pb dating of zircon from two eclogite samples yielded consistent metamorphic ages of 16.7 ± 0.6 Ma and 17.1 ± 0.4 Ma respectively. The metamorphic zircon grew concurrently with Grt II in the peak eclogite facies. Thongmön eclogites characterized by the prograde metamorphism from amphibolite facies to eclogite facies were formed by the continuing continental subduction of Indian plate beneath the Euro‐Asian continent in the Miocene.  相似文献   

17.
非平衡结构代表的变质反应性质和多种矿物地质温压计的研究表明,北京太古宙密云杂岩西段第二期区域变质作用的退变质P-T轨迹具等压冷却特点。Sm-Nd同位素定年显示,区内广泛发育的石榴石冠状体形成于(1717±34)Ma.初步分析认为,P-T-t轨迹的地球动力学成因可与吕梁运动期间华北地台裂谷作用和同构造壳下岩浆增生的演化背景相联系。  相似文献   

18.
The P–T–t path of high‐P metamorphic rocks in subduction zones may reveal valuable information regarding the tectonic processes along convergent plate boundaries. Herein, we present a detailed petrological, pseudosection modelling and radiometric dating study of several amphibole schists of oceanic affinity from the Lhasa Block, Tibet. The amphibole schists experienced an overall clockwise P–T path that was marked by post‐Pmax heating–decompression and subsequent isothermal decompression following the attainment of peak high‐P and low‐T conditions (~490°C and 1.6 GPa). Pseudosection modelling shows that the amphibole schists underwent water‐unsaturated conditions during prograde metamorphism, and the stability field of the assemblage extends to lower temperatures and higher pressures within the water‐unsaturated condition relative to water‐saturated model along the prograde path. The high‐P amphibole schists were highly reduced during retrograde metamorphism. Precise evaluation of the ferric iron conditions determined from the different compositions of epidote inclusions in garnet and matrix epidote is crucial for a true P–T estimate by garnet isopleth thermobarometry. Lu–Hf isotope analyses on garnet size separates from a garnet‐bearing amphibole schist yield four two‐point garnet–whole‐rock isochron ages from 228.2 ± 1.2 Ma to 224.3 ± 1.2 Ma. These Lu–Hf dates are interpreted to constrain the period of garnet growth and approximate the timing of prograde metamorphism because of the low peak metamorphic temperature of the rock and the well‐preserved Mn/Lu growth zoning in garnet. The majority of zircon U–Pb dates provide no constraints on the timing of metamorphism; however, two concordant U–Pb dates of 222.4 ± 3.9 Ma and 223.3 ± 4.2 Ma were obtained from narrow and uncommon metamorphic rims. Coexistence of zircon and sphene in the samples implies that the metamorphic zircon growth was likely assisted by retrogression of rutile to sphene during exhumation. The near coincident radiometric dates of zircon U–Pb and garnet Lu–Hf indicate rapid burial and exhumation of the amphibole schists, suggesting a closure time of c. 224–223 Ma for the fossil ocean basin between the northern and southern Lhasa blocks.  相似文献   

19.
Ultrahigh‐pressure metamorphism (UHPM) has recently been discovered in far‐travelled allochthons of the Scandinavian Caledonides, including finding of diamond in the Seve Nappe Complex. This UHPM of Late Ordovician age is older and less recognized than that in the Western Gneiss Region of southwestern Norway, which was related to terminal collision between Baltica and Laurentia. Here we report new evidence of UHPM in the Lower Seve Nappe, recorded by eclogite and garnet pyroxenite from the area of Stor Jougdan in northern Jämtland, central Sweden. Peak‐metamorphic assemblage of eclogite, garnet + omphacite + phengite + rutile + coesite? yields P–T conditions of 2.8–4.0 GPa and 750–900 °C, constrained by conventional geothermobarometry and thermodynamic modelling in the NCKFMTASH system. The prograde metamorphic evolution of the eclogite is inferred from inclusions of zoisite and amphibole in garnet, which are stable at lower pressure, whereas the retrograde evolution is recorded by formation of diopsidic clinopyroxene + plagioclase symplectites after omphacite, growth of amphibole replacing these symplectites, and of titanite around rutile. In garnet pyroxenite the peak‐metamorphic assemblage consists of garnet + orthopyroxene + clinopyroxene + olivine. P–T conditions of 2.3–3.8 GPa and 810–960 °C have been derived based on the conventional geothermobarometry and thermodynamic modelling in the CFMASH and CFMAS systems. Retrograde evolution has been recognized from replacement of pyroxene and garnet by amphibole. The results show that eclogite was metamorphosed during deep subduction of continental crust, most probably derived from the continental margin of Baltica, whereas the origin and tectonic setting of the garnet pyroxenite is ambiguous. The studied pyroxenite/peridotite of Baltican subcontinental affinity could have been metamorphosed as a part of the subducting plate and exhumed due to the downward extraction of a forearc lithospheric block.  相似文献   

20.
Oxygen isotope ratios of quartz inclusions (QI) within garnet from granulite and amphibolite facies gneisses in the Adirondack Mountains, NY were analysed and used to determine metamorphic temperatures. Primary QI for eight of 12 samples have δ18O values significantly lower than matrix quartz (MQ). The primary QI retain δ18O values representative of thermal conditions during garnet crystallization, whereas the δ18O values of MQ were raised by diffusive exchange with other matrix minerals (e.g. mica and feldspar) during cooling. The δ18O differences between QI and MQ show that garnet (a mineral with slow diffusion of oxygen) can armour QI from isotopic exchange with surrounding matrix, even during slow cooling. These differences between δ18O in MQ and QI can further be used to test cooling rates by Fast Grain Boundary diffusion modelling. Criteria for identifying QI that preserve primary compositions and are suitable for thermometry were developed based on comparative tests. Relations between δ18O and inclusion size, distance of inclusion to host–garnet rim, core–rim zonation of individual inclusions, and presence or absence of petrological features (healed cracks in QI, inclusions in contact with garnet cracks lined by secondary minerals, and secondary minerals along the inclusion grain boundary) were investigated. In this study, 61% of QI preserve primary δ18O and 39% were associated with features that were linked to reset δ18O values. If δ18O in garnet is homogeneous and inclusions are removed, laser‐fluorination δ18O values of bulk garnet are more precise, more accurate, and best for thermometry. Intragrain δ18O(Grt) profiles measured in situ by ion microprobe show no δ18O zonation. Almandine–rich garnet (Alm60–75) from each sample was measured by laser‐fluorination mass‐spectrometry (LF‐MS) for δ18O and compared with ion microprobe measurements of δ18O in QI for thermometry. The Δ18O(Qz–Grt) values for Adirondack samples range from 2.66 to 3.24‰, corresponding to temperatures of 640–740 °C (A[Qz–Alm] = 2.71). Out of 12 samples that were used for thermometry, nine are consistent with previous estimates of peak temperature (625–800 °C) based on petrological and carbon–isotope thermometry for regional granulite and upper amphibolite facies metamorphism. The three samples that disagree with independent thermometry for peak metamorphism are from the anorthosite–mangerite–charnockite–granite suite in the central Adirondacks and yield temperatures of 640–665 °C, ~100 °C lower than previous estimates. These low temperatures could be interpreted as thermal conditions during late (post‐peak) crystallization of garnet on the retrograde path.  相似文献   

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