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1.
We investigated the concentration and site occupation of ferric iron (Fe3+) in (Mg,Fe)O to understand the influence of point defects on transport properties such as atomic diffusion, electrical conductivity and viscosity. We conducted Mössbauer spectroscopy of (Mg0.8Fe0.2)O single crystals synthesized at temperatures from 1673 to 2273 K and pressures from 5 to 15 GPa with Re–ReO2 and Mo–MoO2 oxygen fugacity buffers. The isomer shift of the Mössbauer spectra suggests that Fe3+ occupies mostly the tetrahedral site at reduced conditions and both the octahedral and tetrahedral sites at oxidized conditions. We formulate a thermodynamic model of point defect dissolution in (Mg,Fe)O which suggests that unassociated tetrahedral Fe3+ is more stable than unassociated octahedral Fe3+ at high-pressure and low oxygen fugacity due to the effect of configurational entropy. The pressure dependence of Fe3+ concentration indicates a change in the dominant site occupancy of Fe3+: (1) Fe3+ in the tetrahedral site, (2) Fe3+ in the octahedral site, and (3) defect clusters of Fe3+ and cation vacancy, in the order of increasing oxygen fugacity and decreasing pressure. This is in reasonable agreement with previously reported experiments on Fe3+ concentration, Mg–Fe interdiffusivity and electrical conductivity. We consider it plausible that (Mg,Fe)O accommodates Fe3+ in the tetrahedral site down to the lower mantle. Based on our results and available experimental data, we discuss the solubility competition between Fe3+ and protons (H+), and its implications for transport properties in the lower mantle.  相似文献   

2.
Abundances of transition elements (Ti, V, Cr, Mn, Fe2+, Co, Ni, Cu and Zn) in coexisting clinopyroxene and garnet are used to estimate clinopyroxene/garnet partition coefficients for these elements. The analyzed samples include eclogites, granulites and peridotites. The partition coefficients are sensitive to the major element composition of the mineral phases, although for individual transition elements they correlate with different chemical parameters. The partition coefficients of Ti correlate with the (FeO/MgO)garnet/(FeO/MgO)clinopyroxene ratio thus suggesting that the partitioning of Ti is a sensitive indicator of the physical (temperature-pressure) conditions of equilibration.  相似文献   

3.
Mossbauer spectra of57Fe at 77 and 295°K in the plagioclase from basalts 10044 and 12021 show that iron is in the high-spin ferrous state and located at at least two distinct positions with different coordination numbers. Some excess resonant absorption is probably due to Fe3+ although the Fe3+ doublet could not be positively resolved. The ratio Fe3+/(Fe2+ + Fe3+) is estimated to be between 0.02 and 0.1.  相似文献   

4.
The concentration of rock-forming elements, the static magnetic susceptibility κ, spectra of electron paramagnetic resonance, and their relative intensities I are studied in samples from a borehole drilled in Cenozoic sedimentary deposits of southern Western Siberia. All measured values experience appreciable irregular variations with depth. A linear dependence exists between κ and I within the range of their medium and large values; κ and I have maximum values in the same sample, and κmax = 1920 × 10?6SI, κmin = 210 × 10?6 SI, and κav = 630 × 10?6 SI. The magnetic properties of the samples are controlled by Fe2+ ions present in clastic material and by microphases (clusters) with Fe3+ ions of the goethite and lepidocrocite type present in the cement. The theoretically possible magnetic susceptibility of the Fe2+ ion system (provided that all iron exists in this form) is quite comparable with κmin but, even with very high concentrations of Fe2+, does not reach half of κav: (154 < κ(Fe2+) < 254) × 10?6 SI. Anomalously high values of κ are due to a large number of clusters with Fe3+ ions if structural units FeOOH do not dissociate and the interaction of the clusters with hydroxides of aluminum and precipitation medium impedes the process of their coagulation. Otherwise, the cluster sizes gradually increase, an antiferromagnetic structure develops in clusters, and the magnetic susceptibility decreases.  相似文献   

5.
The oxygen fugacity and therefore the iron redox state of a melt is known to have a strong influence on the liquid line of descent of magmas and thus on the composition of the coexisting melts and crystals. We present a new method to estimate this critical parameter from electron probe microanalyses of two of the most common minerals of basaltic series, plagioclase and clinopyroxene. This method is not based on stoichiometric calculations, but on the different partitioning behaviour of Fe3+ and Fe2+ between both minerals and a melt phase: plagioclase can incorporate more Fe3+ than Fe2+, while clinopyroxene can incorporate more Fe2+ than Fe3+. For example, the effect of oxidizing a partly molten basaltic system (Fe3+ is stabilized with respect to Fe2+) results in an increase of FeOtotal in plagioclase, but a decrease in the associated clinopyroxene. We propose an equation, based on published partition coefficients, that allows estimating the redox state of a melt from these considerations. An application to a set of experimental and natural data attests the validity of the proposed model. The associated error can be calculated and is on average < 1 log unit of the prevailing oxygen fugacity.In order to reduce the number of different variables influencing the Fe2+/Fe3+ mineral/melt equilibrium, our model is restricted to basaltic series with SiO2 < 60% that have crystallized at intermediate to low pressure (< 0.5 GPa) and under relatively oxidizing conditions (?FMQ > 0; where FMQ is the fayalite–magnetite–quartz oxygen buffer equilibrium), but it may be parameterized for other conditions. A spreadsheet is provided to assist the use of equations, and to perform the error propagation analysis.  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.
Bench-scale experiments were conducted to investigate the effect of hydraulic loadings and influent concentration on the migration and biotransformation behaviour of three groundwater pollutants: ammonium (NH4+), iron (Fe2+) and manganese (Mn2+). Columns packed with aquifer media collected from a riverbank filtration (RBF) site in Harbin City, NE China were introduced synthetic groundwater (SGW) or real groundwater (RGW) were at two different constant flow rates and initial contaminant concentrations to determine the impact of system conditions on the fate of the target pollutants biotransformation. The results showed that the biotransformation rate of Fe2+ Mn2+ and NH4+ decreased by 8%, 39% and 15% under high flow rate (50 L d−1) compared to low flow rate (25 L d−1), which was consistent with the residence-time effect. While the biotransformation rate of Fe2+ Mn2+ and NH4+ decreased by 7%, 14% and 9% under high influent concentration comparing with original groundwater. The 16S rRNA analysis of the aquifer media at different depths after experiments completion demonstrated that the relative abundance of major functional microbes iron-oxidizing bacteria and manganese-oxidizing bacteria under higher flow rate and higher influent concentration decreased 13%, 14% and 25%, 24%, respectively, whereas the ammonium-oxidizing bacteria and nitrite-oxidizing bacteria exhibited minimal change, compared to the lower flow rate. Above all results indicated that both high flow rate and high concentration inhibit the biotransformation of NH4+, Fe2+ and Mn2+. The biotransformation of Fe2+ and Mn2+ occurs primarily in the 0–40 cm and 20–60 cm depth intervals, respectively, whereas the NH4+ biotransformation appears to occur relatively uniformly throughout the whole 110 cm column. The biotransformation kinetics of NH4+ in RGW and SGW, Mn2+ in RGW at different depths accords with the first order kinetics model, while Fe2+ in RGW and SGW, Mn2+ in SGW presented more complicated biotransformation process. The results should improve understanding of the transport and fate of common groundwater pollutants in RBF and other groundwater recharge environments.  相似文献   

8.
Recent studies have indicated that a significant amount of iron in MgSiO3 perovskite (Pv) is Fe3+ (Fe3+/ΣFe = 10–60%) due to crystal chemistry effects at high pressure (P) and that Fe3+ is more likely than Fe2+ to undergo a high-spin (HS) to low-spin (LS) transition in Pv in the mantle. We have measured synchrotron Mössbauer spectroscopy (SMS), X-ray emission spectroscopy (XES), and X-ray diffraction (XRD) of Pv with all iron in Fe3+ in the laser-heated diamond-anvil cell to over 100 GPa. Fe3+ increases the anisotropy of the Pv unit cell, whereas Fe2+ decreases it. In Pv synthesized above 50 GPa, Fe3+ enters into both the dodecahedral (A) and octahedral (B) sites approximately equally, suggesting charge coupled substitution. Combining SMS and XES, we found that the LS population in the B site gradually increases with pressure up to 50–60 GPa where all Fe3+ in the B site becomes LS, while Fe3+ in the A site remains HS to at least 136 GPa. Fe3+ makes Pv more compressible than Mg-endmember below 50 GPa because of the gradual spin transition in the B site together with lattice compression. The completion of the spin transition at 50–60 GPa increases bulk modulus with no associated change in density. This elasticity change can be a useful seismic probe for investigating compositional heterogeneities associated with Fe3+.  相似文献   

9.
黑臭现象在我国东部地区浅水湖泊频繁发生,已经严重影响环湖地区的社会经济发展.厌氧环境和高浓度Fe~(2+)、S~(2-)是引起黑臭现象的必要条件.本文解析巢湖南淝河口区黑臭水团范围内Fe~(2+)、S~(2-)与DO、流速的分布特性;基于空间计量模型重点探讨了流速、DO和Fe~(2+)、S~(2-)分布的空间关联性.结果发现,水体流动在黑臭水团中主要有两个作用:使Fe~(2+)、S~(2-)和DO彼此产生空间相关性以及通过分散作用改变局部Fe~(2+)、S~(2-)浓度分布;同时流速通过增强复氧间接影响Fe~(2+)及S~(2-)总体浓度的作用较小.流速与Fe~(2+)、S~(2-)之间均满足线性空间滞后模型;而线性回归模型中流速对Fe~(2+)的影响低估了约7%,对S~(2-)的影响则低估了12%.  相似文献   

10.
Phenocrystic chrome spinel crystallized in normal MORB‐type greenstones in the East Takayama area. Associated phenocryst minerals show a crystallization sequence that was olivine first, followed by plagioclase, and finally clinopyroxene. Chrome spinel ranges from 0.54 to 0.77 in Mg/(Mg+Fe2+) and 0.21 to 0.53 in Cr/(Cr+Al); the Fe3+ content varies from 0.07 to 0.22 p.f.u. (O = 4). Significant compositional differences of spinel were observed among the phenocryst mineral assemblages. Chrome spinel in the olivine–spinel assemblage shows a wide range in Cr/(Cr+Al), and is depleted in Fe2+ and Fe3+. Chrome spinel in the olivine–plagioclase–clinopyroxene–spinel assemblage is Fe2+‐ and Fe3+‐rich at relatively high Cr/(Cr+Al) ratios. Basalt with the olivine–plagioclase–spinel assemblage contains both aluminous spinel and Fe2+‐ and Fe3+‐rich spinel. The assumed olivine–spinel equilibrium suggests that chrome spinel in the olivine–spinel assemblage changed in composition from Cr‐ and Fe2+‐rich to Al‐ and Mg‐rich with the progress of fractional crystallization. Chrome spinel in the olivine–plagioclase–clinopyroxene–spinel assemblage, on the other hand, exhibits the reversed variations in Mg/(Mg+Fe2+) and in Cr/(Cr+Al) ratios that decrease and increase with the fractional crystallization, respectively. The entire crystallization course of chrome spinel, projected onto the Mg/(Mg+Fe2+)–Cr/(Cr+Al) diagram, exhibits a U‐turn, and appears to be set on a double‐lane route. The U‐turn point lies in the compositional field of chrome spinel in the olivine–plagioclase–spinel assemblage, and may be explained by plagioclase fractionation that began during the formation of the olivine–plagioclase–spinel assemblage.  相似文献   

11.
The concentrational control of Fe2+ has been studied in the anoxic hypolimnion of an ice-covered lake with special reference to redox equilibria with the suspended phase. The anoxic bottom water formed during ice conditions differed substantially in terms of vertical distributions from that reported from thermally stratified waters. This was particularly evident for the pH and pe gradients. The main process explaining the Fe2+ concentration profile was a diffusional model in which upwards moving Fe2+ met an opposing O2 flux at the redox cline and precipitated as ferric hydroxide. When the anoxic water column is divided into thin stratums an equilibrium reaction between Fe2+ and amorphous FeOOH explained the Fe2+ concentrations in the upper hypolimnion. Increasing supersaturation was observed at greater depths. Similarly equilibration control of the sulfide concentration by Fe2+ could be shown in the lower hypolimnion. Apparent equilibrium constants for FeS and FeOOH have been calculated together with the eddy diffusion coefficient of Fe2+.  相似文献   

12.
Three synthetic Fe3+ bearing λ-Fe2SiO4 were analyzed using electron probe method, and the M?ssbauer spectra of the samples at 298 K, 150 K, and 95 K were measured. Each spectrum at three temperatures is composed of two doublets. These two doublets are assigned to Fe2+ in the octahedral sites and Fe3+ in the tetrahedral sites, respectively. Site occupancies were determined. The results show that Fe3+ and a small amount of Si4+ are in the tetrahedral and octahedral sites, respectively. The average bond lengths of the octahedral and tetrahedral sites were calculated according to the equations primarily given by Hill et al., O’Neill and Navrotsky and modified by the authors. Furthermore, the octahedral and tetrahedral bond lengths were used to calculate cell parameters and oxygen parameters. In addition, Fe3+ line broadening in the M?ssbauer spectra of Fe3+ bearing λ-Fe2SiO4 were interpreted by using the next nearest neighbor effects  相似文献   

13.
Variations in the titanium isotopic ratios of various solar system materials have been reported by three laboratories. In this work we compare these data (including some new Allende inclusion values reported here) on a common basis. The data of all three groups for terrestrial samples have been found to be consistent within about ten parts per ten thousand for all ratios. The considerable disagreement in reported titanium isotopic anomalies for Allende materials has been investigated by renormalization of all published high-precision titanium isotopic ratio data to various bases in order to assess the nature, number, and loci of possible anomalies. On this basis, variations appear to be present in46Ti and47Ti, as well as in50Ti. All materials reported to date can be divided into two main groups, with the only exceptions being about 10% of Allende inclusions. All but one of the materials reported to date are interpretable as mixtures of a material similar to C-1 and varying amounts (up to about 0.5% of50Ti) of a material characterized by50Ti/46Ti?6 and46Ti?47Ti+48Ti+49Ti. Inclusion EK 1-4-1 requires a further component (up to about 0.5%46Ti) characterized by46Ti/47Ti? 1.3and47Ti?48Ti+49Ti+50Ti.  相似文献   

14.
Distinguishing Iron-Reducing from Sulfate-Reducing Conditions   总被引：2，自引：0，他引：2  
Ground water systems dominated by iron‐ or sulfate‐reducing conditions may be distinguished by observing concentrations of dissolved iron (Fe2+) and sulfide (sum of H2S, HS?, and S= species and denoted here as “H2S”). This approach is based on the observation that concentrations of Fe2+ and H2S in ground water systems tend to be inversely related according to a hyperbolic function. That is, when Fe2+ concentrations are high, H2S concentrations tend to be low and vice versa. This relation partly reflects the rapid reaction kinetics of Fe2+ with H2S to produce relatively insoluble ferrous sulfides (FeS). This relation also reflects competition for organic substrates between the iron‐ and the sulfate‐reducing microorganisms that catalyze the production of Fe2+ and H2S. These solubility and microbial constraints operate in tandem, resulting in the observed hyperbolic relation between Fe2+ and H2S concentrations. Concentrations of redox indicators, including dissolved hydrogen (H2) measured in a shallow aquifer in Hanahan, South Carolina, suggest that if the Fe2+/H2S mass ratio (units of mg/L) exceeded 10, the screened interval being tapped was consistently iron reducing (H2～0.2 to 0.8 nM). Conversely, if the Fe2+/H2S ratio was less than 0.30, consistent sulfate‐reducing (H2～1 to 5 nM) conditions were observed over time. Concomitantly high Fe2+ and H2S concentrations were associated with H2 concentrations that varied between 0.2 and 5.0 nM over time, suggesting mixing of water from adjacent iron‐ and sulfate‐reducing zones or concomitant iron and sulfate reduction under nonelectron donor–limited conditions. These observations suggest that Fe2+/H2S mass ratios may provide useful information concerning the occurrence and distribution of iron and sulfate reduction in ground water systems.  相似文献   

15.
ALHA 77005, a shocked achondrite of the shergottite group, is unique in containing cumulus olivine crystals which display a brownish color in thin section. Mössbauer, EPR, and optical spectroscopic studies show the presence of Fe3+ in the olivine. Approximately 4.5 wt.% of the total iron in the olivine (24 wt.% as FeO) is in the trivalent state. The Fe3+ ions preferentially occupy M2 lattice positions. Charge transfer between Fe3+ and Fe2+ as well as between Fe3+ and oxygen ligands causes a broad absorption band in the optical spectrum at high energies which is the reason for the olivine color. It is concluded that the color of the ALHA 77005 olivine is preterrestrial and may be the result of shock-induced oxidation of the olivine crystals on the meteorite parent body.  相似文献   

16.
A simple, low cost, highly effective, and useful Fenton oxidation treatment of synthetic dye bath waste with pickling liquor as a source of iron (Fe2+ catalyst) is reported. Optimizations of contact time, Fe2+ and H2O2 doses are carried out. Oxidative de‐colorization and degradation of Reactive Blue 4 and Reactive Orange 16 was measured in terms of decrease in absorbance at their wavelength of maximum absorption (RB4, 599 nm; and RO16, 493 nm) and also as reduction in chemical oxygen demand (COD). Approximately, 62% COD was removed in 2 h at optimized doses of Fe2+ (8.95 mM) and H2O2 (61.8 mM) by using pickling waste as a source of Fe2+ catalyst. Similar performance efficiency was observed when neat FeSO4 was used as a source of Fe2+, indicating that pickling liquor can be a low cost source of Fe2+ to treat synthetic dye bath waste by Fenton method.  相似文献   

17.
The electron spin resonance spectrum of Fe3+ in a single crystal of forsterite was studied. Two distinct patterns of about equal intensities were observed which are due to Fe3+ at two distinct positions with 4a (M1)and4c (M2or Si) symmetry of Pbnm. The assignment of the 4c pattern to Fe3+ ions at the Si position cannot be excluded by symmetry but it is unlikely. The Hamiltonian parameters A and E/D are consistent with the conclusion that Fe3+ in this crystal is disordered over two distinct octahedral positions.  相似文献   

18.
About 1 mg/g dw Cu2+ and 8 mg/g dw Fe2+ were found in roots of reed plants when fed with heavy metal concentrations of 100 μM Cu2+ and 10 mM Fe2+ under hypoxia. Roots seemed to act as a kind of filter since the amounts in rhizomes were only 0.06 mg Cu2+/g dw and 2 mg Fe2+/g dw. Increased contents of both ions reduced posthypoxic respiration capacity by 40–50% and also the sum of adenylates (ATP, ADP, AMP) by the same order of magnitude, although energy charge values remained above 0.85 in Cu2+ and 0.79 in Fe2+ treatments. Energy metabolism of rhizomes was not affected. Copper and iron contents of roots as well as of rhizomes were high enough to induce oxidative stress when roots were fed with 40 μM Cu2+ and 1 mM Fe2+, respectively.From our results we conclude that increased, but environmentally attainable, amounts of copper and reduced iron ions disturb root energy metabolism, and therefore root functioning and development. Latent injuries, based on oxidative stress, may be harmful for roots and rhizomes under long term exposure.  相似文献   

19.
The oxidation state of iron can significantly influence the physical and chemical properties of lower mantle minerals. To improve methods for estimation of Fe3+/∑Fe, synthetic assemblages of (Mg,Fe)(Si,Al)O3 perovskite and (Mg,Fe)O ferropericlase were synthesised from oxide starting mixtures in Re or Fe capsules at 26 GPa and 1650-1850 °C using a multianvil press. (Mg,Fe)(Si,Al)O3 majorite was also present in some of the run products. Both electron energy loss spectra (EELS) and Mössbauer spectra were measured for each run product, and a robust fitting method was developed for Mössbauer spectra using EELS results as a standard that enabled Fe3+/∑Fe of (Mg,Fe)(Si,Al)O3 perovskite to be determined from Mössbauer spectra of multiphase assemblages. There is a close to linear variation between Fe3+/∑Fe and Al concentration in (Mg,Fe)(Si,Al)O3 perovskite, independent of oxygen fugacity. The concentration of Fe3+ in (Mg,Fe)O increases with increasing iron concentration along curves of constant oxygen fugacity, where higher oxygen fugacity stabilises greater Fe3+ concentrations. Fe2+/Mg partition coefficients calculated from chemical composition data corrected for measured Fe3+/∑Fe showed values nearly identical within experimental error for all samples, and independent of Al concentration and oxygen fugacity. Simple empirical relations were derived to calculate Fe3+/∑Fe in (Mg,Fe)(Si,Al)O3 perovskite and (Mg,Fe)O ferropericlase samples for which no Mössbauer or EELS data were available, and tested by applying them to calculation of Fe2+/Mg partition coefficients from literature data for (Mg,Fe)(Si,Al)O3 perovskite-(Mg,Fe)O assemblages where only total iron concentrations had been measured. Results showed Fe2+/Mg partition coefficients that were equal to existing values within experimental error, hence confirming the validity of the empirical relations.  相似文献   

20.
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   

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