首页 | 本学科首页   官方微博 | 高级检索  
相似文献
 共查询到20条相似文献，搜索用时 15 毫秒
1.
High-pressure and high temperature experiments at 20 GPa on (Mg,Fe)SiO3 have revealed stability fields of two types of aluminium-free ferromagnesian garnets; non-cubic garnet and cubic garnet (majorite). Majorite garnet is stable only within a limited compositional variation, 0.2 < Fe/(Mg + Fe)< 0.4, and in the narrow temperature interval of 200°C around 2000°C, while the stability of non-cubic garnet with more iron-deficient compositions persists up to higher temperatures. These two garnets show fractional melting into iron-deficient garnet and iron-rich liquid, and the crystallization field of cubic garnet extends over Fe/(Mg + Fe)= 0.5. The assemblage silicate spinel and stishovite is a low-temperature phase, which also occurs in the iron-rich portion of the MgSiO3—FeSiO3 system. The sequence as given by the Fe/(Mg + Fe) value for the coexisting phases with the two garnets at 2000°C and 20 GPa is: silicate modified spinel aluminium-free garnets silicate spinel.Natural majorite in shock-metamorphosed chondrites is clarified to be produced at pressures above 20 GPa and temperatures around 2000°C. Similar shock events may cause the occurrence of non-cubic garnet in iron-deficient meteorites. Non-cubic garnet could be a stable phase in the Earth's mantle if a sufficiently low concentration of aluminium is present in the layer corresponding to the stable pressure range of non-cubic garnet. The chemical differentiation by melting in the deep mantle is also discussed on the basis of the present experimental results and the observed coexistence of majorite garnet with magnesiowüstite in chondrites.  相似文献   

2.
Buchitic sedimentary xenoliths, a few centimetres to several decimetres diameter, occur in Recent andesite from Mount Ngauruhoe, Tongariro Volcanic Center, Taupo Volcanic Zone, New Zealand. Bulk chemistry and Sr isotope compositions of the xenoliths indicate that they are greywacke and argillite derived from Mesozoic Torlesse terrane basement that partly underlies the Taupo Volcanic Zone. The xenoliths contain up to 80% glass with quartz, apatite and zircon remaining as unmelted phases. Glasses within the xenoliths are peraluminous (A/CNK = 1.0 − 1.4), have high normative corundum (2–7%), appreciable FeO (2–4 wt.%), MgO (0.2–1.5 wt.%), TiO2 (0.17–0.84 wt.%), relatively high normative An (1.0–5.3%), and do not represent S-type granitic melts. In the argillite the glass has higher amounts of AI2O3, FeO, MgO, CaO and K2O, and has less SiO2 and Na2O than glass in the greywacke. Silica-rich glass (up to 80 wt.% SiO2) surrounds partially melted quartz. Variable glass chemistry reflects the heterogeneous (layered) nature of the xenoliths. Cordierite (Mg/(Mg + Fe + Mn) = 0.78-0.58), orthopyroxene (En43–56), Mg-rich ilmenite, rutile, pleonaste, V-Cr-Ti spinel, and pyrrhotite occur in the glass of the xenoliths. The dominant cordierite, orthopyroxene, spinel assemblage can be accounted for by disequilibrium breakdown reactions under low oxidation conditions < QFM) involving phengite and chlorite which are abundant in Torlesse greywacke and argillite cropping out along the eastern side of the Taupo Volcanic Zone. Comparison with glass compositions and phase relations of disequilibrium melting experiments on Torlesse greywacke and argillite indicates a minimum temperature of 775°C and a maximum pressure of 1.5 kbar for fusion of the xenoliths that underwent a rapid rate of heating at a depth of less than 5 km and a cooling period constrained by the time of quenching when they were erupted.  相似文献   

3.
A suite of ultramafic xenoliths 2–10 cm in size occurs in basanite near Papeete, Tahiti, and consists of spinel lherzolites with minor dunites and wehrlites. Petrographic examination of xenoliths reveals that they are typically coarse grained with well-developed annealed textures. Microprobe analyses of constituent minerals in 11 xenoliths indicate that bulk compositions of xenoliths are magnesian but with significant variability from xenolith to xenolith especially in Fe/Mg and Cr/Al ratios and in absolute amounts of Al2O3 and Cr2O3. Within any single xenolith, however, coexisting minerals are homogeneous and appear to be compositionally equilibrated. Geothermometry of coexisting orthopyroxene and augite indicates temperatures of equilibration of about 1100°C but there is considerable uncertainty in this estimate due to significant non-quadrilateral pyroxene substitutions. There is no accurate way to determine pressures, but the ubiquity of Cr-poor spinel and absence of garnet imply pressures less than about 15–20 kbar.The margins of most xenoliths show significant alteration through reaction with enclosing alkaline magma. Principal reaction features include zoning of spinels and olivines toward compositions in equilibrium with the magma, and reaction-melting of orthopyroxene to a symplectite of olivine plus silica-rich glass. Glass composition profiles across the symplectites indicate that alkalis, titanium and aluminum diffused into the symplectite from the magma and that silica diffused into the magma. All glass analyses show very low iron, magnesium and calcium.Xenolith mineral assemblages and chemistry indicate their origin in the upper mantle at relatively shallow depths. They are therefore not related genetically to the enclosing basanite magma which came from deeper in the mantle, but rather are accidental fragments of country rock picked up by magma on its way to the surface. The details of the reaction features strongly imply that the magma had partially crystallized by the time it reacted with xenoliths, possibly while still in the mantle.  相似文献   

4.
  相似文献   

5.
Phase equilibria in a natural garnet lherzolite nodule (PHN 1611) from Lesotho kimberlite and its chemical analogue have been studied in the pressure range 45–205 kbar and in the temperature range 1050–1200°C. Partition of elements, particularly Mg2+Fe2+, among coexisting minerals at varying pressures has also been examined. High-pressure transformations of olivine(α) to spinel(γ) through modified spinel(β) were confirmed in the garnet lherzolite. The transformation behavior is quite consistent with the information previously accumulated for the simple system Mg2SiO4Fe2SiO4. At pressures of 50–150 kbar, a continuous increase in the solid solubility of the pyroxene component in garnet was demonstrated in the lherzolite system by means of microprobe analyses. At 45–75 kbar and 1200°C, the Fe2+/(Mg + Fe2+) value becomes greater in the ascending order orthopyroxene, Ca-rich clinopyroxene, olivine and garnet. At 144–146 kbar and 1200°C, garnet exhibits the highest Fe2+/(Mg + Fe2+) value; modified spinel(β) and Ca-poor clinopyroxene follow it. When the modified spinel(β)-spinel(γ) transformation occurred, a higher concentration of Fe2+ was found in spinel(γ) rather than in garnet. As a result of the change in the Mg2+Fe2+ partition relation among coexisting minerals, an increase of about 1% in the Fe2SiO4 component in (Mg,Fe)2SiO4 modified spinel and spinel was observed compared with olivine.These experimental results strongly suggest that the olivine(α)-modified spinel(β) transformation is responsible for the seismic discontinuity at depths of 380–410 km in the mantle. They also support the idea that the minor seismic discontinuity around 520 km is due to the superposition effect of two types of phase transformation, i.e. the modified spinel(β)-spinel(γ) transformation and the pyroxene-garnet transformation. Mineral assemblages in the upper mantle and the upper half of the transition zone are given as a function of depth for the following regions: 100–150, 150–380, 380–410, 410–500, 500–600 and 600–650 km.  相似文献   

6.
The morphology and composition of spinel in rapidly quenched Pu’u ’O’o vent and lava tube samples are described. These samples contain glass, olivine phenocrysts (3–5 vol.%) and microphenocrysts of spinel (0.05 vol.%). The spinel surrounded by glass occurs as idiomorphic octahedra 5–50 μm in diameter and as chains of octahedra that are oriented with respect to each other. Spinel enclosed by olivine phenocrysts is sometimes rounded and does not generally form chains. The temperature before quenching was calculated from the MgO content of the glass and ranges from 1150°C to 1180°C. The oxygen fugacity before quenching was calculated by two independent methods and the log fO2 ranged from −9.2 to −9.9 (delta QFM=−1). The spinel in the Pu’u ’O’o samples has a narrow range in composition with Cr/(Cr+Al)=0.61 to 0.73 and Fe2+/(Fe2++Mg)=0.46 to 0.56. The lower the calculated temperature for the samples, the higher the average Fe2+/(Fe2++Mg), Fe3+ and Ti in the spinel. Most zoned spinel crystals decrease in Cr/(Cr+Al) from core to rim and, in the chains, the Cr/(Cr+Al) is greater in the core of larger crystals than in the core of smaller crystals. The occurrence of chains and hopper crystals and the presence of Cr/(Cr+Al) zoning from core to rim of the spinel suggest diffusion-controlled growth of the crystals. Some of the spinel crystals may have grown rapidly under the turbulent conditions of the summit reservoir and in the flowing lava, and the crystals may have remained in suspension for a considerable period. The rapid growth may have caused very local (μm) gradients of Cr in the melt ahead of the spinel crystal faces. The crystals seem to have retained the Cr/(Cr+Al) ratio that developed during the original growth of the crystal, but the Fe2+/(Fe2++Mg) ratio may have equilibrated fairly rapidly with the changing melt composition due to olivine crystallization. Six of the samples were collected on the same day at various locations along a 10-km lava tube and the calculated pre-collection temperatures of the samples show a 5°C drop with distance from the vent. The average Fe2+/(Fe2++Mg) of the spinel in these samples shows a weak positive correlation with decreasing MgO in the glass of these samples. The range in Cr2O3 (0.041–0.045 wt.%) of the glass for these six samples is too small to distinguish a consistent change along the lava tube. The spinel in the Pu’u ’O’o samples shows a zoning trend in a Cr–Al–Fe3+ diagram almost directly away from the Cr apex. This compares with a zoning trend in rapidly quenched MORB samples away from Cr coupled with decreasing Fe3+. The trend away from Cr displayed by spinel in rapidly quenched samples is in marked contrast to the trend of increasing Fe3+ shown by spinel in slowly cooled lava.  相似文献   

7.
Six crystals of green, uvarovite-rich garnet from the Newlands kimberlite have been analysed. The range of Cr2O3 is 10.04–14.04% and CaO is 19.18–25.94% (wt.), and thus they are similar to garnets found in only one other kimberlite province, namely Yakutia. By combining data from both the Russian and South African occurrences, four models are considered for the formation of such garnets. The model which best accounts for the available chemical data, and mode of occurrence, involves formation of the uvarovitic garnets during subsolidus recrystallization of spinel wehrlitic cumulates, which themselves had been produced by a fractionating magma at a depth of about 200–250 km.  相似文献   

8.
Small euhedral chromite crystals are found in olivine macrophenocrysts (Fo80–84) from the basaltic andesites (150 ppm Cr) erupted in 1943–1947, and in orthopyroxene macrophenocrysts of the andesites (75 ppm Cr) erupted in 1947–1952. The majority of the chromite octahedra are 5–20 μm in diameter, and some are found in clusters and linear chains of three or more oriented chromite crystals. The composition of the majority of the chromite grains within olivine and orthopyroxene macrophenocrysts is Fe2+/(Fe2++Mg)=0.5–0.6, Cr/(Cr+Al)=0.5–0.6 and Fe3+/(Fe3++Al+Cr)=0.2–0.3. The chromite crystals in contact with the groundmass are larger, subhedral, and grade in composition from chromite cores to magnetite rims. Comparison of the composition of chromite with those of other volcanic rocks shows that the most primitive Paricutin chromite is richer in total iron and higher in Fe3+/(Fe3++Al+Cr) than primary chromite in most lavas. The linear chains of oriented chromite octahedra are found in olivine and orthopyroxene macrophenocrysts, and in the groundmass. These chromite chains are thought to result from diffusion-controlled crystallization because of the very high partition coefficient (1000) of Cr between chromite and melt. We conclude that chromite was a primary phase in the lavas at the time of extrusion and that magnetite only crystallized after extrusion during cooling of the lava flows. The presence of chromite microphenocrysts in andesitic lavas containing as little as 70 ppm Cr can be explained by dissolved H2O in the melt depressing the liquidus temperature for orthopyroxene such that chromite becomes a liquidus phase. The influence of dissolved H2O can also explain the lack of plagioclase macrophenocrysts in most of the lavas and the relatively high partition coefficient (20) of Ni between olivine and melt and the high partition coefficient (40) of Cr between orthopyroxene and melt. The liquidus temperature of the basaltic andesite is estimated to have been less than 1140°C, assuming H2O>1 wt.%, and the log fO2 to have been above that of the QFM buffer. The chromite and orthopyroxene liquidus temperature of the andesites, assuming H2O>1 wt.%, is estimated to have been 1100°C or less. The derivation of the later andesites from the earlier basaltic andesites has been explained by a combination of fractional crystallization of olivine, orthopyroxene and plagioclase, and assimilation of xenoliths. The significantly lower Cr, Ni and Mg of the andesites may have been in part due to the separation of olivine macrophenocrysts plus enclosed chromite crystals from the earlier basaltic andesites.  相似文献   

9.
A series of spinel-dunites and spinel-pyroxenites is described from the Archaean amphibolite facies terrain of West Greenland. They occur in a disrupted layered sequence with some units reaching pegmatitic proportions and including intergrowths of spinel + olivine and spinel + orthopyroxene. Rare instances of spinel + olivine overgrown by spinel + orthopyroxene are observed which reveal the way-up of the sequence. The textures described are preserved as boudins within metamorphically layered and recrystallised spinel-olivine-orthopyroxene rocks and they clearly represent undeformed primary igneous assemblages.  相似文献   

10.
Anhydrous spinel lherzolite xenoliths from the Shavaryn-Tsaram volcano, which represent unusually clinopyroxenerich samples of upper mantle beneath the Tariat Depression in north-central Mongolia, have particularly low δ18O values of +4.9 to +5.7‰ SMOW. Constituent minerals exhibit small (ca. 0.5–0.7‰) variations in18O content (olivine = +4.6 to +5.3‰, clinopyroxene = +5.6 to +6.1‰, orthopyroxene = +5.8 to +6.5‰), that are unrelated to xenolith modal mineralogy, chemical composition, radiogenic isotope character, or pyroxene equilibration temperature. This O-isotope character of the Tariat xenoliths is interpreted to reflect the closed-system distribution of oxygen isotopes in a slowly cooling mantle diapir emplaced into the lithosphere from a relatively primitive region of the asthenosphere.  相似文献   

11.
Ultrahigh‐temperature (UHT) granulite facies rocks from the Achankovil Shear Zone area and the southern domain of the Madurai Granulite Block in South India contain monazite useful for in situ microprobe U–Pb dating. The UHT rocks examined consist of garnet + cordierite (retrograde) + quartz + mesoperthite + biotite + plagioclase + Fe‐Ti oxides ± orthopyroxene ± sillimanite and accessory zircon and monazite. Sillimanite occurs only as inclusions in garnet. Microstructural observations suggest garnet, orthopyroxene, spinel and mesoperthite are products of peak metamorphism. Post‐peak formation of cordierite ± orthopyroxene ± quartz and cordierite + spinel + Fe‐Ti oxides assemblages is also observed. Geothermobarometry on orthopyroxene and garnet‐orthopyroxene bearing assemblages suggest peak UHT conditions of T = 940–1040°C and P = 8.5–9.5 kbar. This was followed by a retrograde stage of 3.5–4.5 kbar and 720 ± 60°C, estimated from garnet‐cordierite assemblages. A small population of rounded, probably detrital, monazites in these rocks yield ages from Meso‐ to Neoproterozoic indicating a heterogeneous source. The youngest associated spot ages are 660–600 Ma suggesting protolith deposition up to ca 600 Ma. In contrast, the vast majority of monazites that crystallized during the latest metamorphic event show late Neoproterozoic to Cambrian ages. Probability‐density plots of monazite age data show a ‘peak’ between 533 and 565 Ma, but this peak need not reflect a particular thermal event. Collating ages from homogenous metamorphic monazites associated with minerals stable at peak P‐T conditions suggests peak metamorphism in these rocks occurred at 580–600 Ma. Together with a re‐evaluation of available data from adjacent granulite blocks in southern India, these data suggest the main metamorphic event coinciding with the suturing of India with the Gondwana amalgam probably occurred 580–600 Ma. The 500–550 Ma ages commonly reported in previous studies might represent post‐peak thermal events.  相似文献   

12.
Diagnostic mineral assemblages, mineral compositions and zircon SHRIMP U–Pb ages are reported from an ultrahigh‐temperature (UHT) spinel–orthopyroxene–garnet granulite (UHT rock) from the South Altay orogenic belt of northwestern China. This Altay orogenic belt defines an accretionary belt between the Siberian and Kazakhstan–Junggar Plates that formed during the Paleozoic. The UHT rock examined in this study preserves both peak and retrograde metamorphic assemblages and microstructures including equilibrium spinel + quartz, and intergrowth of orthopyroxene, spinel, sillimanite, and cordierite formed during decompression. Mineral chemistry shows that the spinel coexisting with quartz has low ZnO contents, and the orthopyroxene is of high alumina type with Al2O3 contents up to 9.3 wt%. The peak temperatures of metamorphism were >950°C, consistent with UHT conditions, and the rocks were exhumed along a clockwise P–T path. The zircons in this UHT rock display a zonal structure with a relict core and metamorphic rim. The cores yield bimodal ages of 499 ± 8 Ma (7 spots), and 855 Ma (2 spots), with the rounded clastic zircons having ages with 490–500 Ma. Since the granulite was metamorphosed at temperatures >900°C, exceeding the closure temperature of U–Pb system in zircon, a possible interpretation is that the 499 ± 8 Ma age obtained from the largest population of zircons in the rock marks the timing of formation of the protolith of the rock, with the zircons sourced from a ～500 Ma magmatic provenance, in a continental margin setting. We correlate the UHT metamorphism with the northward subduction of the Paleo‐Asian Ocean and associated accretion‐collision tectonics of the Siberian and Kazakhstan–Junggar Plates followed by rapid exhumation leading to decompression.  相似文献   

13.
The effect of manganese on the stability of ferrosilite relative to fayalite + quartz has been experimentally determined to assess its importance to orthopyroxene barometry. Reaction reversals in a piston-cylinder apparatus were obtained to within 0.1-kbar intervals indicating instability of Fs95Rh5 below 10.3, 10.9, 11.4, 12.2, 12.9, 13.7 kbar and Fs90Rh10 below 9.8, 10.4, 10.9, 11.6, 12.4 and 13.2 kbar at 750, 800, 850, 900, 950 and 1000°C, respectively. Each mole % MnSiO3 extends the pyroxene stability by approximately 0.12 kbar relative to FeSiO3. Electron microprobe analyses of run products indicate a small preference of Mn for pyroxene over olivine withKDMn-Feopx-oliv = 1.2?1.5, similar to values observed for natural pairs. Mössbauer spectra are consistent with a random distribution of Mn between the M1 and M2 sites in the orthopyroxene. These experimental data allow downward revision of pressure estimates based on the orthopyroxene barometer in areas where Mn is a significant component in orthopyroxene.  相似文献   

14.
A mixture containing equal amounts of forsterite and grossularite by weight (Fo50Gr50) has been studied at temperatures between 750 and 1400°C under pressures ranging from 6 to 25 kbar in presence of excess water. The assemblages noted under low pressure (<8 kbar) are as follows: Diopsidess+forsteritess+monticellitess+vapor and Diopsidess+forsteritess+monticellitess+liquid+vapor. (ss denotes solid solution) Under intermediate pressures between 8 and 24 kbar following assemblages were noted in the order of increasing temperature: Diopsidess+forsteritess+spinel+vapor, Diopsidess+forsteritess+spinel+liquid+vapor, Diopsidess+forsteritess+liquid+vapor, and Forsteritess+liquid+vapor. At pressures above 24 kbar the assemblages are as follows: Diopsidess+forsteritess+garnet+vapor, Diopsidess+forsteritess+garnet+liquid+vapor, Diopsidess+forsteritess+liquid+vapor, and Forsteritess+liquid+vapor. Electron microprobe analyses of diopside and forsterite crystallized at 1050°C and 23 kbar, show that the former contains 6 to 6.5 wt % of Al2O3 as solid solution whereas the latter incorporates 1.3 wt % of monticellite in solid solution. The monticellite content of forsterite increases at low pressures at a given temperature to about 6 wt % at 1050°C and 6 kbar. The study indicates that forsteritic olivine does not coexist with pure grossularite in the studied temperature and pressure ranges, although the former is in equilibrium with pyrope-rich garnet, containing 23 mole % grossularite. The study supports the conclusion ofWerner andLuth (1973) that the solubility of monticellite in forsterite decreases with increasing pressure at a given temperature. The results of the investigation are also in agreement with the findings ofKushiro andYoder (1966), who noted that spinel peridotites found in folded belts and in alkalic basalts are produced under intermediate pressures, whereas garnet peridotite xenoliths found in kimberlite and in orogenic belts are formed at high pressures.  相似文献   

15.
Grain-specific analyses of Fe–Ti oxides and estimates of eruption temperature (T) and oxygen fugacity (fO2) have been used to fingerprint rhyolitic fall and flow deposits that are important for tephrostratigraphic studies in and around the Taupo volcanic zone of North Island, New Zealand. The analysed Fe–Ti oxides commonly occur in the rims of orthopyroxene crystals and appear to reflect equilibrium immediately prior to eruption because of geochemical correlation with the co-existing glass phase. The composition of the spinel phase is particularly diagnostic of eruptive centre for post-65 ka events and can be used to distinguish many tephra beds from the same volcano. The 29 different units examined were erupted over a wide range in T (690–990°C) and Δ log fO2 (–0.1 to 2.0). These parameters are closely related to the mafic mineral assemblage, with hydrous mineral-bearing units displaying higher fO2. Such trends are superimposed on larger differences in fO2 that are related to eruptive centre. At any given temperature, all post-65 ka Okataina centre tephra have higher fO2 values than post-65 ka Taupo centre tephra. This provides a useful criterion for identifying the volcanic source. There are no temporal T and fO2 trends in the tephra record; over intervals >20 ka, however, tephra sequences from Taupo centre form characteristic T-fO2 buffer trends mirroring the glass chemistry. Individual eruptive events display uniform spinel and rhombohedral phase compositions and thus narrow ranges in T (± <20°C) and log fO2 (± <0.5), allowing these features to identify individual magma batches. These criteria can help distinguish tephra deposits of similar bulk or glass composition that originated from the same volcano. Distal fall deposits record the same T-fO2 conditions as the proximal ignimbrite and enable distal–proximal correlation. Lateral and vertical compositional and T-fO2 variability displayed in large volume (>100 km3) ignimbrites, such as the Oruanui, Rotoiti and Ongatiti, is similar to that found in a single pumice clast and thus mainly reflects analytical error; however, thermal gradients of ca. 50°C may occur in some units. Received: 6 April 1998 / Accepted: 16 June 1998  相似文献   

16.
A 2-mm fragment of an anorthosite was investigated in transmitted light and by high-voltage electron microscopy. A modal composition of 76% plagioclase (anorthite), 23% pyroxene (pigeonite) and about 1% spinel (pleonaste) was deduced. The results indicate a slight olivine-normative chemical composition. The rock is hypidiomorphic to idiomorphic fine-grained with a well-defined parallel-oriented fabric.Under the petrographic microscope, and even in the submicroscopic range, the plagioclase crystals show twinning only along (010) composition planes (predominantly Carlsbad twins). The dislocation density is low and the dominating defect structures are small-angle grain boundaries. The subtexture of the plagioclases is characterized by aI1-P1 phase transformation and by the existence of large antiphase domains.Features indicative of shock were not observed. From the present results it is concluded that the rock fragment is in its original state. Most likely, crystallisation occurred under plutonic conditions in a deep crustal region with the dominant assemblage: plagioclase + pyroxene + spinel.  相似文献   

17.
Garnet compositions are used to understand mantle petrogenesis and to reconstruct the lithostratigraphy of the shallow mantle (<200 km). However, garnets in polymict peridotites from the Kaapvaal craton (>2500 Ma) have a centimeter-scale elemental and stable isotopic variability suggestive of a mixed mantle provenance. The chemical heterogeneity of the garnets is similar to that reported from rocks sampled over a considerable depth and temperature range within the lower lithosphere. For example garnets found in polymict peridotites are similar to garnets found in sheared and granular peridotites, ‘cold’ and ‘hot’ lherzolites, peridotitic (P-type) diamond inclusions, and garnets from polybaric (50-200 km) peridotites (i.e. spinel, garnet and diamond facies). These data indicate that the Kaapvaal cratonic root has been disturbed by complex processes possibly associated with crack propagation and entrainment that juxtaposed garnet-bearing lithologies of diverse petrogenesis, provenance and depth. This has preserved chemical disequilibrium in the high pressure minerals in what is, in effect, a mantle breccia possibly associated with kimberlite precursors.  相似文献   

18.
Compositional zoning patterns of the major elements and REEs in prograde-zoned garnets whose Mg/(Mg + Fe) atomic ratios increase rimward have been widely used to understand the metamorphic P–T–t trajectories, and the diffusion-limited REE-uptake model is a promising way to interpret their growth rates and the REE diffusion kinetics in the low-temperature eclogite. In order to elucidate their growth kinetics with Skora et al.'s (2006) diffusion-limited REE uptake model for prograde-zoned garnets, we examine the trace-element zoning patterns of two prograde-zoned porphyroblastic garnets (~6 mm in size) in low-temperature eclogites from two different localities. Core-to-rim trace-element profiles in a garnet (prp5–9alm61–67sps1–3grs24–30) of a glaucophane-bearing epidote eclogite of Syros (Cyclades, Greece) are characterized by the presence of Y + HREE peaks in the mantle, which might be attributed to a continuous breakdown of the titanite to form rutile during the garnet growth. In contrast, those in a garnet (prp4–7alm61–68sps3–10grs23–24) extracted from a lawsonite-eclogite of the South Motagua Mélange (SMM) (Guatemala) have prominent central peaks of Y + HREEs. Although the REE profiles of both the garnets can be explained by the diffusion-limited uptake, their Mn profiles suggest that their growth-rate laws are different: i.e., diffusion-controlled (Syros) and interface-controlled (SMM). Prior to the model application, we optimize the number of the parameters as the garnet grows with the interface-controlled processes based on the growth Péclet number. In particular, we propose the ratio of the REE diffusivity in the eclogitic matrix to the garnet growth rate as the new parameter. Visualizing the values of the new parameters allows to readily understand the relationship between the REE profiles and the REE-diffusion/garnet-growth kinetics in low-T eclogite. Our model refinement leads to the simple quantitative characterization of core-to-rim REE profiles in garnet in low-temperature eclogites.  相似文献   

19.
Distribution of trace elements in spinel and garnet peridotites   总被引：6，自引：1，他引：5  
The distribution of trace elements in the upper mantle has been discussed on the basis of the trace element abundances in bulk rocks and constituent minerals of two spinel and garnet facies peridotite xenoliths in alkali basalts from eastern China. The data presented are consistent with the suggestion that highly incompatible elements (Rb, Ba, Th, U, Sr, Nb, Ta) mainly reside in intergranular components, and to a lesser extent in fluid inclusions in minerals. The LILE composition in olivine and orthopyroxene can be seriously affected by the presence of fluid inclusions. Consequently the subsolidus partitioning of the LILE cannot be used to infer the olivine-melt and orthopyroxene-melt partition coefficients for these elements. There is a significant difference in (Opx/Cpx)HREE ratios for spinel and garnet peridotites, suggesting a P-T control on equilibrium partition coefficients.  相似文献   

20.
Gabbro xenoliths in a tholeiitic lava of Kahoolawe Island, Hawaii, a 1.3–1.4 Ma shield volcano, are 1–3 cm in size and comprised of plagioclase, clinopyroxene, and orthopyroxene. Gabbro textures — while intergranular and in part subophitic-are open due to 28–48 vol.% of vesicular basalt occupying xenolith space. Vesicles in and around the xenoliths are lined or filled with rhyolitic glass (segregation vesicles). The host is evolved tholeiite (MgO 6.1 wt%) with phenocrysts, microphenocrysts, and glomerocrysts of olivine, clinopyroxene, orthopyroxene, and plagioclase, and megacrysts (1 cm) of plagioclase. The Sr-isotope ratio of one xenolith is 0.70489; the host basalt ratio is 0.70460. Xenolith isotope composition, grain resorption, and clinopyroxene (Fs12.5–15Wo38–35.5), orthopyroxene (Fs19.5–24Wo4.1), and plagioclase (An68–65Or0.8–1.2) compositions suggest that these gabbros crystallized from Kahoolawe tholeiitic magma of essentially the same composition as the host basalt, but pre-dating the magma represented by the host. Based on the absence of intergranular Fe–Ti oxide phases from the pl+cpx+opx assemblages, and the open, vuggy textures, we envision crystallization on a reservoir roof at temperatures >1100°C. Entrainment of gabbro assemblages and plagioclase megacrysts from a roof mush/suspension zone occurred during convection associated with replenishment of the magma reservoir. These open-textured gabbro xenoliths are therefore not fragments of preexisting coarse-grained bodies such as sills or segregation veins. Rhyolitic glass in vesicles represents a gas-effervescence filtration process that forced fractionated residual liquids from the groundmass into voids associated with the xenoliths.Sirrine Environmental Consultants, Fremont, CA 94538  相似文献   

设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号