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1.
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   

2.
The troctolites and olivine‐gabbros from the Dive 6 K‐1147 represent the most primitive gabbroic rocks collected at the Godzilla Megamullion, a giant oceanic core complex formed at an extinct spreading segment of the Parece Vela back‐arc basin (Philippine Sea). Previous investigations have shown that these rocks have textural and major elements mineral compositions consistent with a formation through multistage interaction between mantle‐derived melts and a pre‐existing ultramafic matrix. New investigations on trace element mineral compositions basically agree with this hypothesis. Clinopyroxenes and plagioclase have incompatible element signatures similar to that of typical‐MORB. However, the clinopyroxenes show very high Cr contents (similar to those of mantle clinopyroxene) and rim having sharply higher Zr/REE ratios with respect to the core. These features are in contrast with an evolution constrained by fractional crystallization processes, and suggest that the clinopyroxene compositions are controlled by melt‐rock interaction processes. The plagioclase anorthite versus clinopyroxene Mg#[Mg/(Mg + FeTot)] correlation of the Dive 6 K‐1147 rocks shows a trend much steeper than those depicted by other oceanic gabbroic sections. Using a thermodynamic model, we show that this trend is reproducible by fractionation of melts assimilating 1 g of mantle peridotite per 1 °C of cooling. This model predicts the early crystallization of high Mg# clinopyroxene, consistent with our petrological observation. The melt‐peridotite interaction process produces Na‐rich melts causing the crystallization of plagioclase with low anorthite component, typically characterizing the evolved gabbros from Godzilla Megamullion.  相似文献   

3.
The Oligocene alkaline basalts of Toveireh area (southwest of Jandaq, Central Iran) exhibit northwest–southeast to west–east exposure in northwest of the central‐east Iranian microcontinent (CEIM). These basalts are composed of olivine (Fo70–90), clinopyroxene (diopside, augite), plagioclase (labradorite), spinel, and titanomagnetite as primary minerals and serpentine and zeolite as secondary ones. They are enriched in alkalis, TiO2 and light rare earth elements (La/Yb = 9.64–12.68) and are characterized by enrichment in large ion lithophile elements (Cs, Rb, Ba) and high field strength elements (Nb, Ta). The geochemical features of the rocks suggest that the Toveireh alkaline basalts are derived from a moderate degree partial melting (10–20%) of a previously enriched garnet lherzolite of asthenospheric mantle. Subduction of the CEIM confining oceanic crust from the Triassic to Eocene is the reason of mantle enrichment. The studied basalts contain mafic‐ultramafic and aluminous granulitic xenoliths. The rock‐forming minerals of the mafic‐ultramafic xenoliths are Cr‐free/poor spinel, olivine, Al‐rich pyroxene, and feldspar. The aluminous granulitic xenoliths consist of an assemblage of hercynitic spinel + plagioclase (andesine–labradorite) ± corundum ± sillimanite. They show interstitial texture, which is consistent with granulite facies. They are enriched in high field strength elements (Ti, Nb and Ta), light rare earth elements (La/Yb = 37–193) and exhibit a positive Eu anomaly. These granulitic xenoliths may be Al‐saturated but Si‐undersaturated feldspar bearing restitic materials of the lower crust. The Oligocene Toveireh basaltic magma passed and entrained these xenoliths from the lower crust to the surface.  相似文献   

4.
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   

5.
Along the east coast of the Andaman Islands, abundant detrital chromian spinels frequently occur in black sands at the confluence of streams meeting the Andaman Sea. The mineral chemistry of these detrital chromian spinels has been used in reconstructing the evolutionary history of the Andaman ophiolite. The chromian spinels show wide variation in compositional parameters such as Cr# [= Cr/(Cr + A1) atomic ratio] (0.13–0.91), Mg# [= Mg/(Mg + Fe2+) atomic ratio] (0.23–0.76), and TiO2 (<0.05–3.9 wt%). The YFe3+[= 100Fe3+/(Cr + A1 + Fe3+) atomic ratio] is remarkably low (usually <10 except for south Andaman). The ranges of chemical composition of chromian spinels are different in each locality. The spinel compositions show very depleted signatures over the entire island, which suggests that all massifs in the Andaman ophiolite were affected under island‐arc conditions. Although the degree of depletion varies in different parts of the island, a directional change in composition of the detrital chromian spinels from south to north is evident. Towards the north the detrital chromian spinels point to less‐depleted source rocks in contrast to relatively more depleted towards the south. The possibilities to explain this directional change are critically discussed in the context of the evolution of Andaman ophiolite.  相似文献   

6.
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   

7.
Abstract The Permian ophiolite emplaced in the Yakuno area, Kyoto Prefecture, consists of metavolcanic sequences, metagabbro and a troctolitic intrusion. The metavolcanics are associated with thick mudstone through a contact that shows the flowage of lava over unconsolidated mud layers on the sea floor. The metavolcanics and metagabbro have rare earth element (REE) patterns that are similar to enriched (E)‐ and transitional (T)‐types ([La/Yb]N = 0.77–11.2) of mid‐oceanic ridge basalts (MORB), whereas their Nb/La ratios (0.40–1.20) are as low as those of back‐arc basin basalts (BABB). Cr‐spinels in the metavolcanic rocks have Cr? of 40–73 and an Fe3+? of 9–24, numbers which are comparable to the values of BABB. These lines of evidence suggest that the Yakuno ophiolite originated more likely from an early stage back‐arc basin rather than from an oceanic plateau, as has been suggested by some researchers. The troctolitic body that intrudes as a 0.5‐km long lens in the metagabbro is composed of troctolite, olivine gabbro and microgabbro. The troctolite is marked by an olivine–plagioclase crystallization sequence, different from the commonly observed olivine–clinopyroxene sequence in other mafic/ultramafic cumulates of the Yakuno ophiolite. The microgabbro, with a composition close to that of the parental magma of the troctolite, is depleted in light REE ([La/Yb]N = 0.18–0.55) so that it has an REE pattern that mimics normal (N)‐type MORB. The interstitial clinopyroxene of the troctolite has highly variable TiO2 contents (0.2–1.4 wt%), which is interpreted to result from postcumulus crystallization of heterogeneous intercumulus melts. The troctolitic intrusion may represent a late stage intrusion that formed in an off‐ridge environment during sea floor spreading of the back‐arc basin. The geochemical variation observed in the Yakuno ophiolite, ranging from N‐ to E‐MORB affinities, reflects the changes in both mantle source compositions and processes involved in magma generation during the evolution of the back‐arc basin.  相似文献   

8.
Many isolated grains of a reddish pleonaste-type spinel occur in fines and metabreccia samples, particularly 14 319. Electron microprobe analyses (104) of spinels and their associated phases include 58 of pleonaste which show Mg/(Mg + Fe) 0.44–0.62 and Cr/(Cr + Al) 0.017–0.134 (atomic), plus minor amounts of other ions, and differ greatly from almost all previously recorded lunar spinels; almost no spinels of intermediate composition were found. Two types of compositional zoning exist: a diffuse primary one with cores lower in Ti, and a narrow secondary one from reaction with matrix yielding rims higher in Cr, Ti, and Mn. At contacts with breccia matrix there is a narrow corona of almost pure plagioclase (An80-An94), free of opaque minerals and pyroxene. Two types of solid inclusions found in the pleonaste are calcic plagioclase, and tiny spherical masses of nickel-rich sulfide.  相似文献   

9.
This study is focused on a plagioclase‐bearing spinel lherzolite from Chah Loqeh area in the Neo‐Tethyan Ashin ophiolite. It is exposed along the west of left‐lateral strike‐slip Dorouneh Fault in the northwest of Central‐East Iranian Microcontinent. Mineral chemistry (Mg#olivine < ~ 90, Cr#clinopyroxene < ~ 0.2, Cr#spinel < ~ 0.5, Al2O3orthopyroxene > ~ 2.5 wt%, Al2O3clinopyroxene > ~ 4.5 wt%, Al2O3spinel > ~ 41.5 wt%, Na2Oclinopyroxene > ~ 0.11 wt%, and TiO2clinopyroxene > ~ 0.04 wt%) confirms Ashin lherzolite was originally a mid‐oceanic ridge peridotite with low degrees of partial melting at spinel‐peridotite facies in a lithospheric mantle level. However, some Ashin lherzolites record mantle upwelling and tectonic exhumation at plagioclase‐peridotite facies during oceanic extension and diapiric motion of mantle along Nain‐Baft suture zone. This mantle upwelling is evidenced by some modifications in the modal composition (i.e. subsolidus recrystallization of plagioclase and olivine between pyroxene and spinel) and mineral chemistry (e.g. increase in TiO2 and Na2O of clinopyroxene, and TiO2 and Cr# of spinel and decrease in Mg# of olivine), as a consequence of decompression during a progressive upwelling of mantle. Previous geochronological and geochemical data and increasing the depth of subsolidus plagioclase formation at plagioclase‐peridotite facies from Nain ophiolite (~ 16 km) to Ashin ophiolite (~ 35 km) suggest a south to north closure for the Nain‐Baft oceanic crust in the northwest of Central‐East Iranian Microcontinent.  相似文献   

10.
Tholeiitic basalt glasses from the FAMOUS area of the Mid-Atlantic Ridge are among the most primitive basaltic liquids reported from the ocean basins. One of the more primitive of these[Mg/(Mg+Fe2+) = 0.68;Ni= 232ppm;TiO2 = 0.61] glasses (572-1-1) was selected for an experimental investigation. This study found olivine to be the liquidus phase from 1 atm to 10.5 kbar where it is replaced by clinopyroxene. The sequence of appearance of phases at 1 atm pressure is olivine (1268°C), plagioclase (1235°C) and clinopyroxene (1135°C). The sample is multiply saturated at 10.5 kbar with olivine (Fo88), clinopyroxene (Wo32En60Fs9), and orthopyroxene (Wo5En83Fs12). From the 1-atm data we have measured (FeO/MgO) olivine/(FeO*/MgO) liquid (K′D) for olivine-melt pairs equilibrated at 12 temperatures in the range 1268–1205°C.K′D varies from 0.30 at 1205°C to 0.27 at 1268°C. Analysis of high-pressure olivine melt pairs indicates a systematic increase inK′D with pressure.Evaluation of the 1-atm experiments reveals that fractionation of olivine followed by olivine + plagioclase can generate much of the variation in major element chemistry observed in the FAMOUS basalt glasses. However, it cannot account for the entire spectrum of glass compositions — particularly with respect to TiO2 and Na2O. The variations in these components are such as to require different primary liquids.Comparison of clinopyroxene microphenocrysts/xenocrysts found in oceanic tholeiites with experimental clinopyroxenes reveal that the majority of those in the tholeiites may have crystallized from the magma at pressures greater than ～ 10 kbar and are not accidental xenocrysts. Clinopyroxene fractionation at high pressures may be a viable mechanism for fractionating basaltic magmas.The major and minor element mineral/meltK′d's from our experiments have been used to model the source region residual mineralogy for given percentages of partial melting. These data suggest that ～20% partial melting of a lherzolite source containing 0–10% clinopyroxene can generate the major and minor element concentrations in the parental magmas of the Project FAMOUS basalt glasses.  相似文献   

11.
Yongfeng Zhu 《Island Arc》2008,17(4):560-576
A study of potassium‐ and silica‐rich glass (SiO2 = 65.3–67.4%, K2O = 7.1–9.8%, Na2O = 4.4–6.5%) in spongy clinopyroxene rims from anhydrous spinel harzburgite, collected from Damaping (Hannuoba, north China), is reported here. The corroded surface of clinopyroxene along with clear chemical zonation (homogeneous core and partially melted rim) suggests that incongruent melting of primary clinopyroxene is responsible for generating the Si‐rich glass in clinopyroxene rims. The degree of clinopyroxene melting is estimated to be higher than 15%. In order to generate glass with K2O contents of 7.0 to 9.8% by clinopyroxene melting at a degree of 15% in a closed system, K2O contents in the primary clinopyroxene should be greater than 1.0 wt%, suggesting a very deep origin for the Damaping harzburgite.  相似文献   

12.
Geochemical data are presented for a suite of ultramafic and related rocks from the Dras ophiolitic melange of the Indus suture zone in the western Himalaya. Harzburgites from the suite have highly refractory chemistry. Lherzolites from the suite represent modified mantle material and are comparable to potential source rocks for MORB and to the lherzolites of the Bay of Islands ophiolites. Cumulus dunite, pyroxenite and gabbro units contain olivine, chromite, clinopyroxene and plagioclase as the major cumulus phases. Orthopyroxene is absent as a cumulus phase and in this respect the Dras ophiolite differs from the Marum, Betts Cove and Troodos ophiolites. However, the Dras cumulates are similar to the Vourinos and Bay of Islands cumulate sequence and are consistent with accumulation of low-pressure liquidus phases of mid-oceanic ridge-type magmas. Magmas parental to the Dras cumulate rocks contained high 100 Mg/(Mg + Fe2+) ratios of 77–79, high Ni, Cr and possibly Ca, low Ti and depleted LREE. Parent magmas were probably similar to those of normal MORB formed by two-stage (or dynamic) melting processes in the mantle. Peridotite fabrics suggest high-temperature plastic (mantle) deformation. Disruption, serpentinisation and melange formation were probably produced during emplacement in the Indus suture zone.  相似文献   

13.
Three groups of spinels have been identified in dredged basalts from the Mid-Atlantic Ridge in the Azores region (30–40°N): (1) magnesiochromites with 0.4–0.5 Cr/(Cr + Al) are most common and characteristic of olivine tholeiites of the region; (2) titaniferous magnesiochromites are found in an olivine basalt with alkali affinities, of local occurrence and evolved in relatively high fugacity of oxygen; (3) chromian spinels with 0.23 Cr/(Cr + Al) occur in unusual high-Al picrites of local occurrence and possible high-pressure origin. Spinels are restricted in occurrence to the least fractionated lavas, with FeO*/FeO* + MgO ratio less than 0.575 and with Cr content greater than 350 ppm. A close relationship between Al content of liquidus spinel and Al content of magma has been observed for basaltic types. High-Al spinels deviating from this relationship, such as those found in picritic lavas from the Mid-Atlantic Ridge, may have crystallized at high pressure. The use of spinels as geobarometers in magmas of a restricted compositional range seems a promising prospect. There is no evidence of systematic variation in spinel chemistry of occurrence along the Mid-Atlantic Ridge, such as could be related to different mantle sources of the basalts, plume versus non-plume or binary mantle mixing.  相似文献   

14.
During a 52-day eruption in 1256 A.D., 0.5 km3 of alkali-olivine basalt was extruded from a 2.25-km-long fissure at the north end of the Harrat Rahat lava field, Saudi Arabia. The eruption produced 6 scoria cones and a lava flow 23 km long that approached the ancient and holy city of Madinah to within 8 km. Three chemical types of basalt are defined by data point clusters on variation diagrams, i.e. the low-K, high-K, and hybrid types. All three erupted simultaneously. Their distribution is delineated in both scoria cones and lava flow units from detailed mapping and a petrochemical study of 135 samples. Six flow units, defined by distinct flow fronts, represent extrusive pulses. The high-K type erupted during all six pulses, the low-K type during the first three, and the hybrid type during the first two.Three mineral assemblages occur out of equilibrium in all three chemical types.Assemblage 1 contains resorbed olivine and clinopyroxene megacrysts and ultramafic microxenoliths (Fo90 + Cr spinel + Cr endiopside) which fractionated within the spinel zone of the mantle.Assemblage 2 contains resorbed plagioclase megacrysts (An60) with olivine inclusions (Fo78) which fractionated in the crust.Assemblage 3 contains microphenocrysts of plagioclase and olivine in a groundmass of the same minerals with late-crystallizing titansalite and titanomagnetite; assemblage 3 crystallized at the surface and/or in the upper crust. Each assemblage represents a distinct range in PTX environment, suggesting that their coexistence in each chemical type may be a function of magma mixing. Such a process is confirmed by variable ratios of incompatible element pairs in a range of analyses.All three chemical types are products of mixing. Some of the hybrid types may have developed from surface mixing of the low-K and high-K lavas; however, the occurrence of all three types at the vent system suggests that subsurface mixing was the dominant process. We suggest that the Madinah flow was extruded from a heterogeneous magma chamber containing vertically stacked sections equivalent to the six eruptive pulses. This chamber may have developed contemporaneously with magma mixing when a crustal reservoir containing a magma in equilibrium with assemblage 2 was invaded by a more primitive magma containing cognate microxenoliths and megacrysts of assemblage 1.  相似文献   

15.
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16.
Late Cenozoic alkali basalts in the Ganseong area of South Korea contain abundant ultramafic xenoliths and clinopyroxene megacrysts. Anhydrous clinopyroxene‐rich wehrlite–clinopyroxenites make up the majority of the xenolith population and range from wehrlite through olivine clinopyroxenite to clinopyroxenite. This study investigates the petrogenesis of wehrlite–clinopyroxenite xenoliths and clinopyroxene megacrysts on the basis of petrography and mineral and whole‐rock chemistry. Observations such as an absence of carbonate or apatite, high Ti/Eu ratio, and clinopyroxene‐dominated mineralogy lead us to rule out peridotite–melt reactions as the origin of the Ganseong wehrlites– olivine clinopyroxenites. The whole‐rock compositions (e.g. high abundance of CaO at a given MgO content and low abundance of incompatible elements, such as U, K, P, and Ti compared with mafic melts) indicate that the pyroxenites do not represent crystallized magma itself, but are rather cumulates with a small amount of residual liquid. Anhydrous and orthopyroxene‐free mineral assemblages, crystallization sequence of olivine→clinopyroxene→plagioclase, and mineral chemistries (e.g. low Cr# and high TiO2 abundances in spinels and high TiO2 and Na2O abundances in clinopyroxenes at a given Mg#) suggest that relatively anhydrous intraplate alkaline basalt is the most likely candidate for the parent magma. Texture and compositions of the clinopyroxene megacrysts preclude a cognate origin via high‐pressure crystallization of the host magma. The clinopyroxene megacrysts occupy the Fe‐rich end of the compositional trends defined by wehrlite–pyroxenite clinopyroxenes. Progressive decreases in Mg# and an absence of significant compositional gaps between pyroxenite xenoliths and clinopyroxene megacrysts indicate fractionation and differentiation of a similar parental magma. We suggest that the clinopyroxene megacrysts represent fragments of pegmatitic clinopyroxenites crystallized from more advanced fractionation stages of the evolution of a series of magmatic liquids formed Ganseong wehrlite–clinopyroxenites.  相似文献   

17.
Lamellar inclusions of chromian spinel (Cr/Cr + Al> 0.7), clinopyroxene and chromian spinel-clinopyroxene symplectite occur in olivines from alpine-type peridotites which have equilibrated at relatively low temperature (<700°C). They occur most commonly in dunite with very magnesian olivine (Fo93 to Fo95) and discrete grains of Cr-rich spinel. Olivine which initially equilibrated with magnesian and Cr-rich liquid had contained small amounts of calcium and trivalent chromium in the octahedral site, and lamellar chromian spinel and diopsidic clinopyroxene exsolved during the annealing process. The ordinary depletion of chromium or absence of chromian spinel lamellae in olivines in igneous rocks may be partly due to the effective exclusion of chromium from olivine upon cooling.  相似文献   

18.
Fawzy F.  Abu El Ela  Esam S.  Farahat 《Island Arc》2010,19(1):151-164
Podiform chromitites hosted in serpentinites (after harzburgite and dunite) and talc‐carbonate rocks from the Abu Meriewa–Hagar Dungash district (MHD), Eastern Desert of Egypt, together with metagabbros, pillow metavolcanics, and metasediments, form an ophiolitic mélange formed during the Neoproterozoic Pan‐African Orogeny. The chromitites show massive, disseminated, and nodular textures. Chromite cores in chromitites have high and restricted ranges of Cr# (0.65–0.75) and Mg# (0.64–0.83), implying primary compositions not affected by metamorphism. Therefore, they are used as reliable indicators of parent magma composition and tectonic affinities of these highly metamorphosed rocks. On the contrary, the altered rims are high‐Cr, low‐Fe3+ spinel (rather than ferritchromit) enriched in Cr, Fe, and Mn, and depleted in Al and Mg (Cr# = 0.75–0.97, Mg# = 0.29–0.79), due to equilibration with interstitial silicates during regional metamorphism up to transitional greenschist–amphibolite facies at about 500–550°C. The primary chromite compositions suggest derivation from a high‐Mg tholeiitic, to possibly boninitic, parental magma in a supra‐subduction zone (arc–marginal basin) environment, similar to the spatially associated metavolcanic rocks. The MHD chromitites are most probably formed by melt–rock interaction mechanisms. The high Cr# of the investigated chromites suggests high degrees of partial melting of a depleted harzburgite source by interaction with primitive basaltic melt of deeper origin followed by mixing. Such Cr‐rich chromites are common in chromitites from the Eastern Desert of Egypt, implying broad thermal anomalies, possibly linked to an important geodynamic feature of the Arabian–Nubian Shield (ANS) evolution. This could revive interest in models that involve asthenospheric uprise, related to plume interaction or most probably due to oblique convergence of arc terranes during early evolution of the ANS.  相似文献   

19.
The extinct Pleistocene volcano Muriah, situated behind the main Pleistocene—Recent Sunda magmatic arc in north-central Java, has erupted at least two contrasted groups of lavas. One group forms a well-defined compositional series (Anhydrous Series) from leucite basanite to tephritic phonolite, with olivine and tschermakitic clinopyroxene the main phenocrysts. The other group, the “Hydrous Series”, includes compositionally variable tephrites and high-K andesites with common plagioclase, biotite and amphibole. Lavas of the Anhydrous Series are much richer in LIL trace elements than the most potassic lavas of neighbouring active volcanoes, but relative HFS element enrichment is less pronounced. REE patterns have almost constant slopes from La (250–600 times chondrites) to Yb (5–10 times chondrites), while those of lavas of active centres are less light-enriched, and show flattening in the heavy REE. Anhydrous Series initial 87Sr/86Sr ratios (0.7043–0.7046) are lower than those of active centres (0.7047–0.7053). Hydrous Series lavas are intermediate in all these geochemical characteristics.The most mafic A-series leucite basanite, with Mg/(Mg + Fe2+) 0.69, 140 ppm Ni and 620 ppm Cr was probably derived from the primary magma for the series by fractionation of only 5 wt.% olivine. Its REE pattern suggests derivation from a garnet-bearing source. Experiments on this basanite, with up to 10% olivine and 20% orthopyroxene added, and in the presence of H2O and H2O/CO2 mixtures, have shown that for all but very high magma water contents, the olivine and garnet liquidus fields are widely separated by fields of phlogopite and clinopyroxene. There is no liquidus field of orthopyroxene. Hence, if magma production involved an equilibrium melting process alone, the most probable sources are of garnet-bearing phlogopite clinopyroxenite type. Alternatively, this magma may represent the end-product of interaction between a low-K basanite magma from a garnet lherzolite source in the asthenosphere and a phlogopite-bearing lherzolite zone in the lower lithosphere. Its production was probably related to crustal doming and extension superimposed on the dominant subduction regime. Hydrous Series magmas may have resulted from mixing between Anhydrous Series magmas and high-K calc-alkaline basaltic to andesitic magmas more directly related to subduction processes.  相似文献   

20.
Peridotites exposed in the Yugu area in the Gyeonggi Massif, South Korea, near the boundary with the Okcheon Belt, exhibit mylonitic to strongly porphyroclastic textures, and are mostly spinel lherzolites. Subordinate dunites, harzburgites, and websterites are associated with the lherzolites. Amphiboles, often zoned from hornblende in the core to tremolite in the rim, are found only as neoblasts. Porphyroclasts have recorded equilibrium temperatures of about 1000°C, whereas neoblasts denote lower temperatures, about 800°C. Olivines are Fo90–91 in lherzolites and Fo91 in a dunite and a harzburgite. The Cr# (= Cr/(Cr + Al) atomic ratio) of spinels varies together with the Fo of olivines, being from 0.1 to 0.3 in lherzolites and around 0.5 in the dunite and harzburgite. The Na2O content of clinopyroxene porphyroclasts is relatively low, around 0.3 to 0.5 wt% in the most fertile lherzolite. The Yugu peridotites are similar in porphyroclast mineral chemistry not to continental spinel peridotites but to sub‐arc or abyssal peridotites. Textural and mineralogical characteristics indicate the successive cooling with hydration from the upper mantle to crustal conditions for the Yugu peridotites. Almost all clinopyroxenes and amphiboles show the same U‐shaped rare earth element (REE) patterns although the level is up to ten times higher for the latter. The hydration was associated with enrichment in light REE, resulting from either a slab‐derived fluid or a fluid circulating in the crust. The mantle‐wedge or abyssal peridotites were emplaced into the continental crust as the Yugu peridotite body during collision of continents to form a high‐pressure metamorphic belt in the Gyeonggi Massif. The peridotites from the Gyeonggi Massif exhibit lower‐pressure equilibration than peridotites, with or without garnets, from the Dabie–Sulu Collision Belt, China, which is possibly a westward extension of the Gyeonggi Massif.  相似文献   

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