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1.
The exsolutious of diopside and magnetite occur as intergrowth and orient within olivine from the mantle dunite, Luobusa ophiolite, Tibet. The dunite is very fresh with a mineral assemblage of olivine （〉95%） ＋ chromite （1%-4%） ＋ diopside （〈1%）. Two types of olivine are found in thin sections： one （Fo = 94） is coarse-grained, elongated with development of kink bands, wavy extinction and irregular margins; and the other （Fo = 96） is fine-grained and poly-angied. Some of the olivine grains contain minor Ca, Cr and Ni. Besides the exsolutions in olivine, three micron-size inclusions are also discovered. Analyzed through energy dispersive system （EDS） with unitary analytical method, the average compositions of the inclusions are： Na20, 3.12%-3.84%; MgO, 19.51%-23.79%; Al2O3, 9.33%-11.31%; SiO2, 44.89%-46.29%; CaO, 11.46%-12.90%; Cr2O3, 0.74%-2.29%; FeO, 4.26%- 5.27%, which is quite similar to those of amphibole. Diopside is anhedral f＇dling between olivines, or as micro-inclusions oriented in olivines. Chromite appears euhedral distributed between olivines, sometimes with apparent compositional zone. From core to rim of the chromite, Fe content increases and Cr decreases; and A! and Mg drop greatly on the rim. There is always incomplete magnetite zone around the chromite. Compared with the nodular chromite in the same section, the euhedral chromite has higher Fe3O4 and lower MgCr2O4 and MgAI2O4 end member contents, which means it formed under higher oxygen fugacity environment. With a geothermometer estimation, the equilibrium crystalline temperature is 820℃-960℃ for olivine and nodular chromite, 630℃-770℃ for olivine and euhedral chromite, and 350℃-550℃ for olivine and exsoluted magnetite, showing that the exsolutions occurred late at low temperature. Thus we propose that previously depleted mantle harzburgite reacted with the melt containing Na, Al and Ca, and produced an olivine solid solution added with Na^＋, Al^3＋, Ca^2＋, Fe^3＋, Cr^3＋. With temperature d  相似文献   

2.
The ultramafic member of the Variscan Ślęża Ophiolite (SW Poland) consists of heavily serpentinised, refractory harzburgites. Those located down to 1.5 km below paleo-Moho contain scarce grains or aggregates of olivine, clinopyroxene and spinel. Non-serpentine phases occur in various assemblages: M1—olivine (Fo 90.2–91.0%, NiO 0.38–0.47 wt.%) and rounded or amaeboidal aluminous chromite, rimmed by Al poor chromite and magnetite; M2—olivine (Fo 90.5–91.5, NiO 0.32–0.44 wt.%), olivine with magnetite inclusions (Fo 87.1–92.5, NiO 0.01–0.68 wt.%), rounded, cleavaged clinopyroxene I (Mg# 91.1–93.2, Al2O3 3.00–4.00 wt.%, Cr2O3 1.00–1.40 wt.%) and elongated clinopyroxene II and clinopyroxene from symplectites with magnetite (Mg# = 92.2–94.1, Al2O3 2.20–3.20 wt.% and Cr2O3 0.80–1.20 wt.%). Clinopyroxene is depleted in REEs relative to chondrite. The M3 assemblage consists of intergrown olivine (Fo 90.8–92.7, NiO 0.20–0.38 wt.%) and clinopyroxene (Mg# = 96.0–98.1, Al2O3 0.00–1.00 wt.% and Cr2O3 0.20–0.60 wt.%).The M1 assemblage contains chromite which records greenschist-facies metamorphism. Textural relationships and chemical composition of clinopyroxene occurring in the M2 assemblage are similar to those formed in oceanic spreading centres by LREE depleted basaltic melt percolation. Olivine occurring in M1 assemblage and part of that from M2 have composition typical of residual olivine from the abyssal harzburgites and of olivine formed in those rocks by melt percolation. The olivine with magnetite inclusions (M2 assemblage) and that from M3 record later deserpentinization event, which supposedly produced also M3 clinopyroxene. The non-serpentine phases from the Ślęża ophiolite mantle member, albeit very poorly preserved, document depleted basaltic melt percolation in the Variscan oceanic spreading centre.  相似文献   

3.
This paper reports detailed studies on harzburgite and serpentinite in the Hegenshan ophiolitic mélange. Harzburgite consists mainly of olivine and orthopyroxene with trace amounts of clinopyroxene and chromian spinel. Clinopyroxene occurs as isolated crystals or in the intergrowth of chromian spinel–clinopyroxene–orthopyroxene. Harzburgite is moderately to highly depleted, displaying high Fo contents in olivine (90.8–92.2), moderate Al2O3 contents in orthopyroxene (1.59–2.79 wt%), low heavy REE abundances in clinopyroxene, and moderate Cr# values of spinel (0.50–0.62). The modal proportions of olivine and orthopyroxene pseudomorph grains imply that the parent of the Hegenshan serpentinite should be harzburgite. Whole-rock compositions of the harzburgite and serpentinite samples are characterized by depletions in Al2O3 and CaO and enrichments in light REE, Sr, and U. Geochemical modeling suggests that the Hegenshan harzburgite represents residues after 17–18% partial melting of the primitive mantle. The melt in equilibrium with clinopyroxene is more depleted than typical forearc basalt and boninite. Various pyroxene thermobarometers yield equilibrated temperatures of 945–1067 °C and pressures of 4.8–8.0 kbar for the Hegenshan harzburgite. The oxygen barometer yields results of +0.4 to +1.7 log units above the fayalite–magnetite–quartz buffer for the Hegenshan harzburgite. These petrological and geochemical characteristics, as well as the estimated P–T–fO2 conditions support a back-arc setting for the Hegenshan ophiolitic mélange.  相似文献   

4.
ABSTRACT

We investigated lherzolitic peridotites in the Cretaceous Purang ophiolite along the Yarlung Zhangbo suture zone (YZSZ) in SW Tibet to constrain their mantle–melt evolution history. Coarse-grained Purang lherzolites contain orthopyroxene (Opx) and olivine (Ol) porphyroclasts with embayments filled by small olivine (Ol) neoblasts. Both clinopyroxene (Cpx) and Opx display exsolution textures represented by lamellae structures. Opx exsolution (Opx1) in clinopyroxene (Cpx1) is made of enstatite, whose compositions (Al2O3 = 3.85–4.90 wt%, CaO = <3.77 wt%, Cr2O3 = 0.85–3.82 wt%) are characteristic of abyssal peridotites. Host clinopyroxenes (Cpx1) have higher Mg#s and Na2O, with lower TiO2 and Al2O3 contents than Cpx2 exsolution lamellae in Opx, and show variable LREE patterns. Pyroxene compositions of the lherzolites indicate 10–15% partial melting of a fertile mantle protolith. P–T estimates (1.3–2.3 GPa, 745–1067°C) and the trace element chemistry of pyroxenes with exsolution textures suggest crystallization depths of ~75 km in the upper mantle, where the original pyroxenes became decomposed, forming exsolved structures. Further upwelling of lherzolites into shallow depths in the mantle resulted in crystal–plastic deformation of the exsolved pyroxenes. Combined with the occurrence of microdiamond and ultrahigh-pressure (UHP) mineral inclusions in chromites of the Purang peridotites, the pyroxene exsolution textures reported here confirm a multi-stage partial melting history of the Purang lherzolites and at least three discrete stages of P-T conditions in the course of their upwelling through the mantle during their intra-oceanic evolution.  相似文献   

5.
Mid-ocean ridge basalts (MORBs) from East Pacific Rise (EPR) 13°N are analysed for major and trace elements, both of which show a continuous evolving trend. Positive MgO–Al2O3 and negative MgO–Sc relationships manifest the cotectic crystallization of plagioclase and olivine, which exist with the presence of plagioclase and olivine phenocrysts and the absence of clinopyroxene phenocrysts. However, the fractionation of clinopyroxene is proven by the positive correlation of MgO and CaO. Thus, MORB samples are believed to show a “clinopyroxene paradox”. The highest magnesium-bearing MORB sample E13-3B (MgO=9.52%) is modelled for isobaric crystallization with COMAGMAT at different pressures. Observed CaO/Al2O3 ratios can be derived from E13-3B only by fractional crystallization at pressure >4 ±1 kbar, which necessitates clinopyroxene crystallization and is not consistent with cotectic crystallization of olivine plus plagioclase in the magma chamber (at pressure ~1 kbar). The initial compositions of the melt inclusions, which could represent potential parental magmas, are reconstructed by correcting for post-entrapment crystallization (PEC). The simulated crystallization of initial melt inclusions also produce observed CaO/Al2O3 ratios only at >4±1 kbar, in which clinopyroxene takes part in crystallization. It is suggested that MORB magmas have experienced clinopyroxene fractionation in the lower crust, in and below the Moho transition zone. The MORB magmas have experienced transition from clinopyroxene+plagioclase+olivine crystallization at >4±1 kbar to mainly olivine+plagioclase crystallization at <1 kbar, which contributes to the explanation of the “clinopyroxene paradox”.  相似文献   

6.
The Dangqiong ophiolite, the largest in the western segment of the Yarlung-Zangbo Suture Zone(YZSZ)ophiolite belt in southern Tibet, consists of discontinuous mantle peridotite and intrusive mafic rocks. The former is composed dominantly of harzburgite, with minor dunite, locally lherzolite and some dunite containing lenses and veins of chromitite. The latter, mafic dykes(gabbro and diabase dykes), occur mainly in the southern part. This study carried out geochemical analysis on both rocks. The results show that the mantle peridotite has Fo values in olivine from 89.92 to 91.63 and is characterized by low aluminum contents(1.5–4.66 wt%) and high Mg# values(91.06–94.53) of clinopyroxene. Most spinels in the Dangqiong peridotites have typical Mg# values ranging from 61.07 to 72.52, with corresponding Cr# values ranging from 17.67 to 31.66, and have TiO2 contents from 0 to 0.09%, indicating only a low degree of partial melting(10–15%). The olivine-spinel equilibrium and spinel chemistry of the Dangqiong peridotites suggest that they originated deeper mantle(20 kbar). The gabbro dykes show N-MORB-type patterns of REE and trace elements. The presence of amphibole in the Dangqiong gabbro suggests the late-stage alteration of subduction-derived fluids. All the lherzolites and harzburgites in Dangqiong have similar distribution patterns of REE and trace elements, the mineral chemistry in the harzburgites and lherzolites indicates compositions similar to those of abyssal and forearc peridotites, suggesting that the ophiolite in Dangqiong formed in a MOR environment and then was modified by late-stage melts and fluids in a suprasubduction zone(SSZ) setting. This formation process is consistent with that of the Luobusa ophiolite in the eastern Yarlung-Zangbo Suture Zone and Purang ophiolite in the western Yarlung-Zangbo Suture Zone.  相似文献   

7.
The Mazaertag layered intrusion is located in the northwestern part of the Tarim large igneous province where several early Permian layered mafic-ultramafic intrusions host important Fe-Ti oxide deposits. The intrusion covers an area of ～0.13 km~2 and has a vertical stratigraphic thickness of at least300 m. It consists chiefly of olivine clinopyroxenite, and is cut through by the nearby mafic-ultramafic dykes. In this paper, we report new mineral chemistry data and whole-rock chemical and isotopic compositions for the Mazaertag intrusion along with whole-rock isotopic compositions for the nearby mafic dykes. The averaged compositions of cumulus olivine, clinopyroxene and intercumulus plagioclase within individual samples range from Fo_(71-73),Mg~# = 76 to 79 and An_(65-75) but they do not define sustained reversals. The observed mineral compositions are consistent with the differentiation of a single batch of magma in a closed system. Rocks of the Mazaertag intrusion are characterized by enrichment in light REE relative to heavy REE, positive Nb and Ta anomalies and a small range of age-corrected ε_(Nd)(t)(-0.1 to +0.9) and initial ~(87)Sr/~(86)Sr values(0.7044 to 0.7068). The slightly lower ε_(Nd)(t), initial ~(206)Pb/~(204)Pb and higher initial ~(87)Sr/~(86)Sr values of the intrusion compared to those of the least contaminated dykes[ε_(Nd)(t) =+2.8 to +3.4;(~(206)Pb/~(204)Pb)_i = 18.516-18.521;(~(87)Sr/~(86)Sr)_i = 0.7038-0.7041] imply that the Mazaertag magma was subjected to small to modest degrees of contamination by the upper crust. The Sr-Nd isotopic compositions of the least contaminated dykes are consistent with derivation from a FOZO-like mantle source. The parental magma of the Mazaertag intrusion, estimated from clinopyroxene compositions using mineral-melt partition coefficients, has trace element compositions similar to some of the most primitive mafic dykes in the same area. This suggests that the Mazaertag intrusion and mafic dykes shared a similar mantle source. Therefore, the parental magma of the Mazaertag intrusion was interpreted to have originated from a mantle plume. Based on the Cr_2 O_3 contents in titanomagnetite and less-evolved characteristics of the Mazaertag intrusion compared to the Wajilitag Fe-Ti oxide deposit in Bachu, it is speculated that there might not be a potential to find economic Fe-Ti oxide mineralization in the intrusion.  相似文献   

8.
The Shirokaya Salma eclogite‐bearing complex is located in the Archean–Palaeoproterozoic Belomorian Province (Russia). Its eclogites and eclogitic rocks show multiple clinopyroxene breakdown textures, characterized by quartz–amphibole, orthopyroxene and plagioclase lamellae. Representative samples, a fresh eclogite, two partly retrograded eclogites, and a strongly retrograded eclogitic rock, were collected for this study. Two distinct mineral assemblages—(1) omphacite+garnet+quartz+rutile±amphibole and (2) clinopyroxene+garnet+amphibole+plagioclase+quartz+rutile+ilmenite±orthopyroxene—are described. Based on phase equilibria modelling, these assemblages correspond to the eclogite and granulite facies metamorphism that occurred at 16–18 kbar, 750–800°C and 11–15 kbar, 820–850°C, respectively. The quartz–amphibole lamellae in clinopyroxene formed during retrogression with water ingress, but do not imply UHP metamorphism. The superfine orthopyroxene lamellae developed due to breakdown of an antecedent clinopyroxene (omphacite) during retrogression that was triggered by decompression from the peak of metamorphism, while the coarser orthopyroxene grains and rods formed afterwards. The P–T path reconstructed for the Shirokaya Salma eclogites is comparable to that of the adjacent 1.9 Ga Uzkaya Salma eclogite (Belomorian Province), and those of several other Palaeoproterozoic high‐grade metamorphic terranes worldwide, facts allowing us to debate the exact timing of eclogite facies metamorphism in the Belomorian Province.  相似文献   

9.
Textural and mineral–chemical characteristics in the Bangriposi wehrlites (Eastern India) provide insight into metamorphic processes that morphologically and chemically modified magmatic spinel during serpentinization of wehrlite. Aluminous chromite included in unaltered magmatic olivine is chemically homogenous. In sub-cm to 10s-of-micron-wide veins, magnetite associated with antigorite and clinochlore comprising the serpentine matrix is near-stoichiometric. But Al–Cr–Fe3+ spinels in the chlorite–magnetite veins are invariably zoned, e.g., chemically homogenous Al-rich chromite interior successively mantled by ferritchromite/Cr-rich magnetite zone and magnetite continuous with vein magnetite in the serpentine matrix. In aluminous chromite, ferritchromite/Cr-rich magnetite zones are symmetrically disposed adjacent to fracture-controlled magnetite veins that are physically continuous with magnetite rim. The morphology of ferritchromite–Cr-rich magnetite mimics the morphology of aluminous chromite interior but is incongruous with the exterior margin of magnetite mantle. Micropores are abundant in magnetite veins, but are fewer in and do not appear to be integral to the adjacent ferritchromite–Cr-rich magnetite zones. Sandwiched between chemically homogenous aluminous chromite interior and magnetite mantle, ferritchromite–Cr-rich magnetite zones show rim-ward decrease in Cr2O3, Al2O3 and MgO and complementary increase in Fe2O3 at constant FeO. In diffusion profiles, Fe2O3–Cr2O3 crossover coincides with Al2O3 decrease to values <0.5 wt% in ferritchromite zone, with Cr2O3 continuing to decrease within magnetite mantle. Following fluid-mediated (hydrous) dissolution of magmatic olivine and olivine + Al–chromite aggregates, antigorite + magnetite and chlorite + magnetite were transported in 10s-of-microns to sub-cm-wide veins and precipitated along porosity networks during serpentinization (T: 550–600 °C, f(O2): ?19 to ?22 log units). These veins acted as conduits for precipitation of magnetite as mantles and veins apophytic in chemically/morphologically modified magmatic Al-rich chromite. Inter-crystalline diffusion induced by chemical gradient at interfaces separating aluminous chromite interiors and magnetite mantles/veins led to the growth of ferritchromite/Cr-rich magnetite zones, mimicking the morphology of chemically modified Al–Cr–Fe–Mg spinel interiors. Inter-crystalline diffusion outlasted fluid-mediated aluminous chromite dissolution, mass transfer and magnetite precipitation.  相似文献   

10.
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   

11.
ABSTRACT

A chromite deposit was discovered in the Kudi ophiolite in the Palaeozoic western Kunlun orogenic belt. Chromite forms elongated (<2 m in width) and banded chromitite bodies (<0.1 m in width for each band) in dunite and podiform chromitite bodies (<1.5 m in width) in harzburgite. Dunite is classified into two types. Type I dunite hosting massive and banded chromitites shows low Fo in olivine (88.1–90.9), moderate Cr# [=Cr/(Cr + Al), 0.47–0.56] in chromite, and a positively sloped primitive mantle-normalized platinum group elements (PGE) pattern, suggesting that it is a cumulate of a mafic melt. Harzburgite and type II dunite show olivine with high Fo (>91.1) and chromite with moderate to high Cr# (0.44–0.61), and flat to negatively sloped primitive mantle-normalized PGE patterns, indicating that they are residual mantle peridotite after partial melting. Chromite in all three types of chromitites has relatively uniform moderate values Cr# ranging from 0.43 to 0.56. Massive chromitite contains euhedral chromite with high TiO2 (0.40–0.43 wt.%) and has a positively sloped primitive mantle-normalized PGE pattern, suggesting that it represents a cumulate of a melt. Rocks containing disseminated and banded chromite show overall low total PGE, < 117 ppb, and a negatively sloped primitive mantle-normalized PGE pattern. Chromite grains in these two types of occurrences are irregular in shape and enclose olivine grains, suggesting that chromite formed later than olivine. We suggest that chromite-oversaturated melt penetrated into the pre-existing dunite and crystallized chromite. The oxygen fugacity (fO2 values of chromitites and peridotites are high, ranging from FMQ+0.8 (0.8 logarithmic unit above the fayalite-magnetite-quartz buffer) to FMQ+2.3 for chromitites and from FMQ+0.9 to FMQ+2.8 for peridotites (dunite and harzburgite). The mineral compositions and high fO2 values as well as estimated parental magma compositions of the chromitites suggest that the Kudi ophiolite formed in a sub-arc setting.  相似文献   

12.
We present the whole rock and the mineral chemical data for upper mantle peridotites from the San-Jiang region in Yunnan, SW China. These peridotites are a part of a Paleo-Tethyan ophiolite belt occurring along the Jinshajiang and Lancangjiang suture zones. All samples of the Jinshajiang and Lancangjiang ultramafic rocks are completely serpentinized. The Jinshajiang serpentinites are characterized by no relict of olivine and pyroxene, and the Cr# content of spinels is 0.32–0.49. The Lancangjiang serpentinites were collected from two different locations; the northern location which has some relict of Opx(Al2O3 is 0.13–2.2 wt%, TiO 2 is 0.004–0.057 wt% and Mg# content is 0.895–0.933) and the Cr# content of spinel is 0.26-0.55; the southern location, which has some relict of Olivine(Fo = 90–92.5 and NiO = 0.12–0.26 wt%), and spinel Cr# ranging from 0.41 to 0.57. The whole rock geochemical and the mineral chemistry data imply that the Jinshajiang and Lancangjiang serpentinites represent abyssal peridotites residues after ~15–20% partial melting for the Jinshajiang and Lancangjiang serpentinites(south location), and ~11–19% partial melting for the Lancangjiang serpentinites(north location). In addition, the compositional trends of the spinel analyses of the Lancangjiang serpentinites imply that the MORB melt-peridotite interaction process played a significant role during their evolution. These processes are evidenced by an increase in Cr# with an increase in TiO 2, whereas the spinel analyses of the Jinshajiang serpentinites display an increase in Cr# with a decrease in Ti O2, indicating that the Jinshajiang serpentinites were subjected to a simple partial melting process.  相似文献   

13.
Archaean banded iron formation (BIF) of the Voronezh Crystalline Massif (VCM) contains coexisting clino‐ and orthopyroxenes with exsolution textures. The pyroxene in the VCM BIF is found in two generations, with only the first generation containing such textures. Clinopyroxene contains large (up to 5–10 μm) (0 0 1) orthopyroxene (Opx1L) lamellae in a host clinopyroxene (Cpx1H). This host Cpx, in turn, exsolves into thin (～1 μm) (1 0 0) lamellae of orthopyroxene (Opx2L) and clinopyroxene (Cpx2H). Orthopyroxene exhibits similar exsolution textures with large (up to 50 μm) (0 0 1) clinopyroxene (Cpx1L) lamellae developed in a host orthopyroxene (Opx1H). This clinopyroxene Cpx1L shows further exsolution of thin (1 0 0) Opx2LL lamellae and clinopyroxene (Cpx2LH). Point microprobe analysis, raster‐mode microprobe analysis, and microprobe element mapping of mineral grains with a large number of point analysis were used to determine the composition of the exsolution products and the primary chemistry of the coexisting clinopyroxene (CaO = 14.86–17.26 wt%) and pigeonite (CaO = 4.45–6.23 wt%). These pyroxenes crystallized during the peak of metamorphism, and application of the Lindsley geothermometer suggested that they formed at extremely high temperatures of about 1000 °C. Primary very dense CO2‐rich fluid inclusions (ρ = 1.152 g cm?3, Th = ?49.2 °C) were discovered for the first time in these BIF. With these data, the metamorphic pressure was estimated as 10–11 kbar (depth 36–40 km). Such ultrahigh temperature–high pressure (UHT–HP) conditions for the regional metamorphism of the Precambrian BIF have previously been reported only for Archaean meta‐ironstone from the Napier Complex (Enderby Land, Antarctica). They give an insight into the peak metamorphic conditions of the BIF of the VCM, their burial under thickened continental crust during this period of Earth evolution and suggest a more complicated multistage metamorphic and tectono‐thermal history for the region than has previously been postulated.  相似文献   

14.
Detailed microtextural observations and bulk chemical analysis were undertaken on a garnet‐pyroxenite nodule within retrograde eclogites from the NE Sulu ultrahigh‐pressure metamorphic (UHPM) terrane. The results suggest that the protolith was a cumulate from a gabbroic body. The nodule consists primarily of coarse clinopyroxene grains with a very high content of the Ca‐Tschermakite molecule. Microscopic observations and back‐scattered electron images (BSE) demonstrate a complicated intergrowth of clinopyroxene, garnet and ilmenite, which represents the peak metamorphic assemblage. The primary clinopyroxene grains are armoured with a thin garnet corona up to 0.5 mm wide that forms an interconnected network. Within the clinopyroxene grains, four sets of garnet lamellae are distributed along crystallographic planes; locally, a vermicular intergrowth of garnet and diopside is developed. Besides the garnet, parallel arrays of ilmenite blebs are common within the clinopyroxene. Hydrous minerals such as amphibole, zoisite and titanite formed at later stages, and replaced diopside, garnet and ilmenite respectively. The P–T conditions determined for the formation of the garnet lamellae indicate that the garnet pyroxenite experienced UHP metamorphism at the same peak P–T condition as its host eclogite. The very high Ca‐Tschermakite content (31–34 mol.%) of the primary clinopyroxene indicates crystallization at about 9–17 kbar and 1250–1450 °C, and together with the microtextural observations, suggests that the protolith of the garnet pyroxenite was a cumulate from a former gabbroic body, in which case, the host eclogite might represent the gabbroic body.  相似文献   

15.
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   

16.
西藏罗布莎蛇绿岩中不同产出的纯橄岩及成因探讨   总被引：2，自引：2，他引：0  
罗布莎蛇绿岩中的纯橄岩有三种产出情况,除了与豆荚状铬铁矿伴生的薄壳状纯橄岩外,还有产在方辉橄榄岩底部被认为是堆晶岩的厚层状纯橄岩和方辉橄榄岩中的透镜状纯橄岩。厚层状纯橄岩约700～1000m厚,以橄榄石富镁(Fo93～95),单斜辉石低铝富镁(Al2O30.47%～0.85%,Mg#95～97),铬尖晶石高铬低镁(Cr#值平均77,Mg#平均51)为特征。该纯橄岩中的浸染状铬铁矿也是高铬低镁型,但Mg#值(平均59)高于厚层状纯橄岩的副矿物铬尖晶石。薄壳状纯橄岩与厚层状纯橄岩成分相近,其橄榄石Fo92～94,单斜辉石Al2O3<1%和Mg#95～97;铬尖晶石的Cr#值平均71,Mg#值平均52。与薄壳状纯橄岩伴生的块状铬铁矿为高镁高铬型,但Mg#值(平均68)相对更高些,Cr#值平均79。透镜状纯橄岩的特征是橄榄石Fo(91～92)和铬尖晶石Cr#(60左右)均低于前两类纯橄岩,但单斜辉石的Al2O3(1.41%～1.71%)则高于前两者。透镜状纯橄岩的矿物成分与方辉橄榄岩重叠,两者为渐变过渡关系。研究对比表明,罗布莎厚层状纯橄岩不同于经典的蛇绿岩的超镁铁质堆晶岩,认为将其成因解释为拉斑玄武质熔体与地幔橄榄岩的反应较为合理。透镜状纯橄岩与方辉橄榄岩存在成生联系,可能是地幔橄榄岩高度部分熔融的产物,或熔体和方辉橄榄岩在原位发生反应的产物;薄壳状纯橄岩成因与厚层状纯橄岩相同,但与其相伴的块状铬铁矿是否由拉斑玄武质熔体与方辉橄榄岩反应形成,值得商榷。  相似文献   

17.
The Benjamin River apatite prospect in northern New Brunswick, Canada, is hosted by the Late Silurian Dickie Brook plutonic complex, which is made up of intrusive units represented by monzogranite, diorite and gabbro. The IOA ores, composed mainly of apatite, augite, and magnetite at Benjamin River form pegmatitic pods and lenses in the host igneous rocks, the largest of which is 100 m long and 10–20 m wide in the diorite and gabbro units. In this study, 28 IOA ore and rock samples were collected from the diorite and gabbro units. Mineralogical observations show that the apatite–augite–magnetite ores are variable in the amounts of apatite, augite, and magnetite and are associated with minor amounts of epidote‐group minerals (allanite, REE‐rich epidote and epidte) and trace amounts of albite, titanite, ilmenite, titanomagnetite, pyrite, chlorite, calcite, and quartz. Apatite and augite grains contain small anhydrite inclusions. This suggests that the magma that crystallized apatite and augite had high oxygen fugacity. In back scattered electron (BSE) images, apatite grains in the ores have two zones of different appearance: (i) primary REE‐rich zone; and (ii) porous REE‐poor zone. The porous REE‐poor zones mainly appear in rims and/or inside of the apatite grains, in addition to the presence of apatite grains which totally consist of a porous REE‐poor apatite. This porous REE‐poor apatite is characterized by low REE (<0.84 wt%), Si (<0.28 wt%), and Cl (<0.17 wt%) contents. Epidote‐group minerals mainly occur in grain boundary between the porous REE‐poor apatite and augite. These indicate that REE leached from primary REE‐rich apatite crystallized as allanite and REE‐rich epidote. Magnetite in the ores often occurs as veinlets that cut apatite grains or as anhedral grains that replace a part of augite. These textures suggest that magnetite crystallized in the late stage. Pyrite veins occur in the ores, including a large amount of quartz and calcite veins. Pyrite veins mainly occur with quartz veins in augite. These textures indicate pyrite veins are the latest phase. Apatite–augite–magnetite ore, gabbro–quartz diorite and feldspar dike collected from the Benjamin River prospect contain dirty pure albite (Ab98Or2–Ab100) under the microscope. The feldspar dikes mainly consist of dirty pure albite. Occurrences of the dirty pure albite suggest remarkable albitization (sodic alteration) of original plagioclase (An25.3–An60 in Pilote et al., 2012) associating with intrusion of monzogranite into gabbro and diorite. SO42? bearing magma crystallized primary REE‐rich apatite, augite and anhydrite reacted with Fe in the sodic fluids, which result in oxidation of Fe2+ and release of S2? into the sodic fluids. REE, Ca and Fe from primary REE‐rich apatite, augite and plagioclase altered by the sodic fluids were released into the fluids. Then Fe3+ in the sodic fluids precipitated as Fe oxides and epidote‐group minerals in apatite–augite–magnetite ores. Finally, residual S2? in sodic fluids crystallized as latest pyrite veins. In conclusion, mineralization in Benjamin River IOA prospect are divided into four stages: (1) oxidized magmatic stage that crystallized apatite, augite and anhydrite; (2) sodic metasomatic stage accompanying alteration of magmatic minerals; (3) oxidized fluid stage (magnetite–epidote group minerals mineralization); and (4) reduced fluid stage (pyrite mineralization).  相似文献   

18.
Whole-rock, major and trace element analyses and microprobe mineral analyses were conducted on serpentinized peridotites recovered from the walls of a MAR (Mid-Atlantic Ridge) 43° N fracture zone. These peridotites are extensively serpentinized; serpentine usually makes up 30–100 vol. percent of the bulk rocks. The relict minerals observed consist mainly of olivine and orthopyroxene with subordinate amounts of clinopyroxene and brown spinel. The range in olivine composition is very limited (Fo91–92). Orthopyroxene forms large, anhedral crystals with clinopyroxene exsolution lamellae and shows undulose extinction with bent cleavages and lamellae. Broad beam microprobe analyses indicate that the composition range of orthopyroxene is also limited (En89.1–87.6Fs8.2-8.0Wo2.7–4.4; Al2O3=1.82–2.64 wt%; Cr2O3=0.63–0.88 wt%). Clinopyroxene tends to fringe large orthopyroxene crystals or fills the interstices between them. The Mg/Fe ratios of clinopyroxene are practically constant; however, the Ca/(Ca + Mg + Fe) ratios range from 0.48 to 0.45. The Cr/(Cr+Al) and Mg/(Mg+ Fe2+) ratios of brown spinel range from 0.57 to 0.36 and 0.69 to 0.56, respectively. The geothermometers utilizing coexisting spinel lherzolite mineral assemblages suggest that the MAR 43° N peridotites attained equilibrium at temperatures from 1100° to 1250° C.Peridotites recovered from the ocean floor are generally considered to have been subjected to partial melting processes and are regarded as residues left after primary magma was removed. Major element chemistry of the MAR 43° N peridotites are compared with those of the ocean-floor ultramafic tectonites reported previously and used together with those published data to demonstrate that the major element abundances of the oceanfloor peridotites define an average trend which is compatible with removal of primary magma from these peridotites at moderate pressures (10–15 kb). Then, the most primitive abyssal tholeiite glasses could be produced by ca. 10% olivine fractionation of such primary magma. Extensive fractionation of olivine and/or orthopyroxene from picritic liquids which are in equilibrium with the lherzolitic or harzburgitic mantle sources at higher pressures (>20 kb) could not yield the majority of the most primitive abyssal tholeiite glasses.  相似文献   

19.
http://www.sciencedirect.com/science/article/pii/S1674987113000303   总被引：4，自引：0，他引：4  
The Xinjie layered intrusion in the Panxi region,SW China,hosts both Fe-Ti oxide and platinum-group element（PGE） sulfide mineralization.The intrusion can be divided,from the base upward,into UnitsⅠ,ⅡandⅢ,in terms of mineral assemblages.UnitsⅠandⅡare mainly composed of wehrlite and clino-pyroxenite, whereas UnitⅢis mainly composed of gabbro.PGE sulfide-rich layers mainly occur in Unit I, whereas thick Fe-Ti oxide-rich layers mainly occur in UnitⅢ.An ilmenite-rich layer occurs at the top of UnitⅠ.Fe-Ti oxides include magnetite and ilmenite.Small amounts of cumulus and intercumulus magnetite occur in UnitsⅠandⅡ.Cumulus magnetite grains are commonly euhedral and enclosed within olivine and clinopyroxene.They have high Cr2O3 contents ranging from 6.02 to 22.5 wt.%,indicating that they are likely an early crystallized phase from magmas.Intercumulus magnetite that usually displays ilmenite exsolution occupies the interstices between cumulus olivine crystals and coexists with interstitial clinopyroxene and plagioclase.Intercumulus magnetite has Cr2O3 ranging from 1.65 to 6.18 wt.%, lower than cumulus magnetite.The intercumulus magnetite may have crystallized from the trapped liquid.Large amounts of magnetite in UnitⅢcontains Cr2O3（<0.28 wt.%） much lower than magnetite in UnitsⅠandⅡ.The magnetite in UnitⅢis proposed to be accumulated from a Fe-Ti-rich melt.The Fe-Ti-rich melt is estimated to contain 35.9 wt.%of SiO2,26.9 wt.%of FeOt,8.2 wt.%of TiO2,13.2 wt.%of CaO, 8.3 wt.%of MgO,5.5 wt.%of Al2O3 and 1.0 wt.%of P2O5.The composition is comparable with the Fe-rich melts in the Skaergaard and Sept Iles intrusions.Paired non-reactive microstructures,granophyre pockets and ilmenite-rich intergrowths,are representative of Si-rich melt and Fe-Ti-rich melt,and are the direct evidence for the existence of an immiscible Fe-Ti-rich melt that formed from an evolved ferro-basaltic magma.  相似文献   

20.
雅鲁藏布江蛇绿岩带是国内铬铁矿床出露点最多,且铬铁矿石储量、产量最大的一个蛇绿岩带。根据空间展布规律,该岩带被划分为东段(曲水—墨脱)、中段(昂仁—仁布)和西段(萨嘎至中印边境)3部分。其中,西段自萨嘎以西分为南、北两支亚带。长期以来的研究工作主要集中在东段和中段,西段的研究程度非常薄弱,尤其是北亚带。不同区段研究程度的不平衡十分不利于雅鲁藏布江蛇绿岩带内铬铁矿找矿工作的开展。错不扎蛇绿岩体位于雅鲁藏布江缝合带西段的北亚带,呈北西-南东向带状产出,主要由方辉橄榄岩组成,并普遍发育基性岩脉。野外地质调查在该蛇绿岩体中发现了多个铬铁矿化点,矿化体呈透镜状产于方辉橄榄岩中,出露地表的长度为0.5～1m,厚为0.2～0.5 m,矿石均为致密块状。电子探针分析结果表明,错不扎铬铁矿属于高铬型铬铁矿,铬尖晶石的Cr#[=100×Cr/(Cr+Al)]为75～78,Mg#[=100×Mg/(Mg+Fe2+)]为66～69。计算结果表明,母岩浆的FeO/MgO比值为0.51～0.65,Al2O3和Ti O2含量分别为11.27%～12.1%和0.19%～0.4%,与玻安质岩浆的化学成分相当。然而,针状单斜辉石出溶体的发现指示错不扎铬铁矿可能还经历了一个深部作用过程。  相似文献   

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