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1.
We have investigated grain boundary diffusion rates in enstatite by heating single crystals of quartz packed in powdered San Carlos olivine (Mg0.90Fe0.10)2SiO4 at controlled oxygen fugacities in the range 10?5.7 to 10?8.7?atm and temperatures from 1350° to 1450?°C for times from 5 to 100?h at 1?atm total pressure. Following the experiments, the thickness of the coherent polycrystalline reaction rim of pyroxene that had formed between the quartz and olivine was measured using backscatter scanning imaging in the electron microprobe. Quantitative microprobe analysis indicated that the composition of this reaction phase is (Mg0.92Fe0.08)2Si2O6. The rate of growth of the pyroxene increases with increasing temperature, is independent of the oxygen fugacity, and is consistent with a parabolic rate law, indicating that the growth rate is controlled by ionic diffusion through the pyroxene rim. Microstructural observations and platinum marker experiments suggest that the reaction phase is formed at the olivine-pyroxene interface, and is therefore controlled by the diffusion of silicon and oxygen. The parabolic rate constants determined from the experiments were analyzed in terms of the oxide activity gradient across the rim to yield mean effective diffusivities for the rate-limiting ionic species, assuming bulk transport through the pyroxene layer. These effective diffusivities are faster than the lattice diffusivities for the slowest species (silicon) calculated from creep experiments, but slower than measured lattice diffusivities for oxygen in enstatite. Thus, silicon grain boundary diffusion is most likely to be the rate-limiting process in the growth of the pyroxene rims. Also, as oxygen transport through the pyroxene rims must be faster than silicon transport, diffusion of oxygen along the grain boundaries must be faster than through the lattice. The grain boundary diffusivity for silicon in orthopyroxenite is then given by D¯gbSiδ=(3.3±3.0)×10?9f0.0O2e?400±65/RT?m3s?1, where the activation energy for diffusion is in kJ/mol, and δ is the grain boundary width in m. Calculated growth rates for enstatite under these conditions are significantly slower than predicted by an extrapolation from similar experiments performed at 1000?°C under high pressure (hydrous) conditions by Yund and Tullis (1992), perhaps due to water-enhancement of diffusion in their experiments.  相似文献   

2.
Melt inclusions in olivine and pyroxene phenocrysts in kersantite and camptonite at Chhaktalao in Madhya Pradesh, India are mainly of the evolved type forming daughter minerals of olivine, pyroxene, plagioclase, spinel, mica, titanomagnetite and sulphides. Heating studies exhibit a temperature range from 1215° to 1245°C for the melt inclusions in olivine in camptonite and 1220–1245°C for olivine in kersantite. The temperature for melt inclusions in pyroxene ranged from 1000° to 1150°C in camptonite and 850–1100°C for pyroxene in kersantite. The bubble inside these melt inclusions is mainly CO2. The Th°C of CO2 into liquid phase occurred between 26° and 31°C in olivine and 25–30°C in pyroxene from kersantite and camptonite. The maximum density estimated is 0.72 g/cm3 and the minimum is 0.45 g/cm3. The depth of entrapment of the melt inclusion is estimated between 10–15 km. The pressure of entrapment of melt inclusion in olvine is 4.6 kbar where as that in pyroxene is 3.7 kbar. The lamprophyres in the Chhaktalao area are considered to be derived from low depth and low pressure region, possibly within spinel lherzolite zone.  相似文献   

3.
In order to test the chronometer qualities of speculante for the (U + Th)/He dating method, 4He release experiments by stepwise heating of two specularites from the Rimbach mineralization locality in the southern Vosgues (France) have been carried out. The diffusion coefficients define linear Arrhenius plots within a temperature interval of 250 to 830 °C, which is suggestive of volume diffusion. Extrapolation of the diffusion behavior to 20° C yields diffusion coefficients (D20 values) smaller than 10?26 [cm2 s?1] for both hematites with activation energies at 116 [kJ/mole]. The results of our study suggest that specularite is a very helium retentive hematite variety which is capable of quantitatively retaining radiogenic helium over geologic periods of time.  相似文献   

4.
Spinel lherzolite found in Damaping, northern Zhangjiakou, Hebei Province occurs as xenoliths in the Hannuoba basalts that consist of alkali basalt and tholeiite. Spinel lherzolites contain 50%–70% olivine (Fo: 90%), 10%–20% clinopyroxene (predominantly Di), 10%–30% orthopyroxene (predominantly En), and less than 5% spinel.3He/4He and40Ar/38Ar ratios in the olivine are 7.56×10−7 and 299.1, respectively.3He/4He and40Ar/38Ar ratios in the orthopyroxene (enstatite) are 9.1×10−7 and 307, respectively. Olivine grains are fractured irregularly, and pyroxene grains characterized by well developed cleavages, which would have resulted from explosion during the rapid eruption of lava from the deep interior to the surface. The lower isotope ratios of helium and argon may indicate that the spinel lherzolite xenoliths were derived from the strongly degassed and depleted upper mantle, and that the mantle is inhomogeneous.3He losses to some extent might affect the helium isotope ratios. The project was financially supported by the National Natural Science Foundation of China (No. 49273185).  相似文献   

5.
About possibility of isotope dating of native gold by the (U-Th)/He method   总被引：2，自引：0，他引：2  
For investigation of helium in native gold, a new measuring complex was created and used: the high sensitivity mass spectrometer MSU-G (ZAO SKB “SPECTRON”). The sensitivity of measuring 4He was 5.3 × 10?13 cm3/g per impulse. Experiments in stepwise heating of samples have been carried out, and the kinetics of radiogenic 4He emanation from native gold was investigated. Migration parameters (activation energy and frequency factor) were determined. Model calculations of stability (closure temperature) of radiogenic 4He in the native gold structure with a given time and temperature of thermal influences were made using the data received. The concentration of 4He in native gold from the original deposit Nesterovskoe is (4.7 ± 0.1) × 10?5 cm3/g in the sample from the placer; from Chudnoe deposit, it is (3.8 ± 0.1) × 10?5 cm3/g; from sulfide deposits of Kitoiskii knot of Eastern Sayani, it is (1.9 ± 0.1) × 10?5 cm3/g; and from the South Muiskii ore region it is (8.7 ± 0.5) × 10?7 cm3/g. The received curve lines of kinetics of 4He emanation from native gold show that radiogenic helium is well bonded in the native gold structure: in all the examined samples, most 4He emanates only by reaching the temperature of 950–1000°C. A specific feature of the kinetics of radiogenic 4He emanation in all examined samples is an outburstlike emanation in the form of a peak of large amplitude in the area of temperatures near the melting temperature point of gold. This is stipulated by the existence of helium bubbles released by metals only while they melt. The spectrum of helium thermal desorption from native gold has a complicated form and is a result of superposition of several peaks. This proves the migration of groups of atoms located in the gold structure in different energy states. Very large values of the activation energy of helium migration from native gold were received: up to 161–176 kcal/mol. Extremely large values of the frequency factor, from 2 × 1018 to 3 × 1032, correspond to such values of activation energies. This is caused probably by helium migration in the form of gas bubbles. The received data indicate the very high stability of the (U-Th)/He isotope system in native gold. Using the (U-Th)/He method of isotope geochronology seems to be very promising for isotope dating of these strategic raw materials.  相似文献   

6.
4He accumulated in fluids is a well established geochemical tracer used to study crustal fluid dynamics. Direct fluid samples are not always collectable; therefore, a method to extract rare gases from matrix fluids of whole rocks by diffusion has been adapted. Helium was measured on matrix fluids extracted from sandstones and mudstones recovered during the San Andreas Fault Observatory at Depth (SAFOD) drilling in California, USA. Samples were typically collected as subcores or from drillcore fragments. Helium concentration and isotope ratios were measured 4?C6 times on each sample, and indicate a bulk 4He diffusion coefficient of 3.5?±?1.3?×?10?C8 cm2?s?C1 at 21°C, compared to previously published diffusion coefficients of 1.2?×?10?C18 cm2?s?C1 (21°C) to 3.0?×?10?C15 cm2?s?C1 (150°C) in the sands and clays. Correcting the diffusion coefficient of 4Hewater for matrix porosity (??3%) and tortuosity (??6?C13) produces effective diffusion coefficients of 1?×?10?C8 cm2?s?C1 (21°C) and 1?×?10?C7 (120°C), effectively isolating pore fluid 4He from the 4He contained in the rock matrix. Model calculations indicate that <6% of helium initially dissolved in pore fluids was lost during the sampling process. Complete and quantitative extraction of the pore fluids provide minimum in situ porosity values for sandstones 2.8?±?0.4% (SD, n?=?4) and mudstones 3.1?±?0.8% (SD, n?=?4).  相似文献   

7.
胡志中  杨波  杜谷  任静  王冠 《岩矿测试》2012,31(1):24-28
(U-Th)/He定年是一种有效的低温热年代学定年技术,现已被广泛应用于地质研究的各个领域,而矿物中4He同位素的有效提取和含量准确测定是该技术的关键。磷灰石和锆石是(U-Th)/He定年最常用的矿物,其4He提取条件及铀钍含量测定方法都较为成熟;而其他矿物(如磁铁矿、橄榄石、针铁矿、石榴子石等)的研究则相对较少。文章介绍了当前国内外(U-Th)/He研究中采用的4He同位素提取方法———真空炉加热法和激光加热法,激光加热法因具有低4He背景值和耗时短的优点而成为主要的提取方法。以磷灰石样品测试为例,介绍了成都地质矿产研究所建立的采用激光加热法和四极杆质谱提取4He同位素及其含量测量过程、含量计算和校正方法。指出未来(U-Th)/He测试技术除继续改进现有分析方法外,应加强对更多不同矿物的测试研究。  相似文献   

8.
The abundances and isotopic compositions of Helium and Argon have been analyzed in a suite of fresh spinel peridotite xenoliths in Cenozoic basalts from the eastern North China Craton (NCC) by step-wise heating experiments, to investigate the nature of noble gas reservoirs in the subcontinental lithospheric mantle beneath this region. The xenoliths include one harzburgite collected from Hebi in the interior of the NCC, two lherzolites from Hannuoba at the northern margin of the craton, and three lherzolites from Shanwang and Nushan on the eastern margin. 3He/4He ratios in most of the xenoliths are similar to those of mid-ocean ridge basalts (MORB) or slightly lower (2–10.5 Ra, where Ra is the 3He/4He ratio of the atmosphere), suggesting mixing of MORB-like and radiogenic components. One olivine separate from Nushan has a helium value of 25.3 Ra, probably suggesting cosmogenic 3He addition. The 40Ar/36Ar ratios vary from atmospheric value (296) to 1625, significantly lower than the MORB value. Available data of the peridotite xenoliths indicate the He and Ar isotopic systematics of the mantle reservoirs beneath the NCC can be interpreted as mixtures of at least three end-members including MORB-like, radiogenic and atmospheric components. We suggest that the MORB-like noble gases were derived from the underlying asthenosphere during mantle upwelling, whereas the radiogenic and recycled components probably were incorporated into the lithospheric mantle during circum-craton subduction of oceanic crust. Available data suggest that the MORB-like fluids are better preserved in the interior of the NCC, whereas the radiogenic ones are more prevalent at the margins. The Paleo-Asian ocean subduction system probably was responsible for the enriched and recycled noble gas signatures on the northern margin of the craton, while the Pacific subduction system could account for the observed He–Ar isotopic signatures beneath the eastern part. Therefore, integration of helium and argon isotopes reflects heterogeneous metasomatism in the lithospheric mantle and demonstrates the critical importance of lithospheric mantle modification related to both circum-craton subduction of oceanic crust and asthenospheric upwelling beneath the eastern NCC.  相似文献   

9.
This study describes two methods (Procedures‐1 and ‐2) for the direct extraction of Au by an inorganic acid mixture (HClO4‐HBr‐HI‐aqua regia) from complex sample matrices. Standard PTFE jars at 200 °C were used to decompose test portions of 0.5–1 g, with subsequent precise and accurate analysis by ICP‐MS without any other preconcentration or separation. Procedure‐1 decomposed samples effectively without the necessity of leaching with HF and was developed for dust samples from e‐waste (electronic waste) processing; however, testing on geological reference materials showed very good results. The analyses of replicate decompositions (n = 5) from both procedures yielded very good precision (< 5% RSD) for most of the reference materials. The accuracy achieved was better than ± 10%, with the exception of NIST SRM 2782 data from Procedure‐1. Two unknown samples of dust from e‐waste processing (P‐1 and VM‐1) exhibited elevated concentrations of Au (21.31–61.64 μg g?1) with precision better than 10% (n = 5). The proposed techniques are simple, sensitive and sparing in the use of chemicals, and are designed for a variety of e‐waste dust samples. No significant influences were observed for the predicted spectral interferences on mass 197Au.  相似文献   

10.
A selective and sensitive method for the extraction and spectrophotometric determination of gold with N,N′‐6,7,9,10,17,18,20,21‐octahydrodibenzo[b,k][1,4,7,10,13,16] hexaoxacyclo‐octadecine‐2,13–diylbis(2‐chloroacetamide) (ODBOCA) is described. The ODBOCA–Au(III) complex was extracted from a slightly acidic aqueous solution (pH 5) into a chloroform layer and then the absorbance of the extract was measured using a UV–Vis spectrophotometer with 1.0 cm quartz cells at 540 nm. An enrichment factor of 200 was achieved. In the chloroform medium at 540 nm, the molar absorptivity and Sandell’s sensitivity were 4.12 × 103 l mol?1 cm?1 and 0.048 μg cm?2, respectively. Beer’s law was obeyed in the range of 0.5–15 μg ml?1 in the measured solution. The relative standard deviation for ten replicate samples at the 1.0 μg ml?1 level was 3.0%. The limit of detection, based on 3s, was 0.5 μg l?1 in the original sample. The effects of pH, ligand concentration and shaking time were studied. The ratio of the metal ion to ligand molecules in the complex was found to be 1:2 according to the Job Method. The effects of interference by a number of metal ions were investigated. The method was verified with certified reference materials and spiked tests, and quantitative recovery values were obtained. The method was fast, accurate, selective and precise, and was applied to the determination of gold in water and ore with good results.  相似文献   

11.
Chemical and isotopic compositions have been measured for N2-He-rich bubbling gases discharging from hot springs in the Hainan Island, Southern China. Observed 3He/4He ratios (0.1–1.3 RA) indicate the occurrence of a mantle component throughout the island, which has been highly diluted by a crustal radiogenic 4He component. The occurrence of mantle-derived helium is high in the northern island (12%–16% of total He) and gradually decreases towards southern coast (1%–3% of total He). Such a distribution pattern is most likely controlled by the Pleocene-Quaternary volcanic activities in the northern island and groundwater circulation along the deep major faults. The 40Ar/36Ar and N2/Ar ratios suggest that N2 and Ar of the hot spring gases are mostly meteoric. Although δ13C values of CO2 (–20‰ to –27‰) with low concentrations are consistent with the biogenic origin, the combination of 3He/4He and d13CCO2 suggests a two end-member mixing of mantle and crustal components with CO2/3He ratios of 2×109 and 8×1011, respectively. However, the low CO2/3He ratios (1–22×106) can not be ascribed in terms of the simple mixing but has to be explained by the addition of radiogenic 4He and loss of CO2 by calcite precipitation in the hydrothermal system, which is most likely controlled by the degree of gas-water-rock interaction.  相似文献   

12.
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   

13.
This article presents new boron concentrations for nine geochemical reference materials (GS‐N, FK‐N, GL‐O, BX‐N, DT‐N, AN‐G, GH, Mica‐Fe, Mica‐Mg). After extraction by a modified pyrohydrolysis technique, boron concentrations were measured by ICP‐MS. The blank levels for the whole procedure were 0.091 ± 0.020 ng ml?1 or 14 ± 5 ng of boron in total. The method was first validated by measuring nine reference materials with known boron concentrations. The determined boron concentrations are all within the range of recommended or published values, which means that the yields were 100%, and show precisions below 10% for samples containing over 2 μg g?1 of boron.  相似文献   

14.
Vacuum crushing is an efficient technique to selectively release the mantle-derived helium component trapped within olivine and pyroxene phenocrysts. However, contrary to previous assumptions, recent studies have shown that this method may liberate significant matrix-sited cosmogenic 3He (3Hec) or radiogenic 4He (4He∗). Because this loss may bias both the determination of magmatic 3He/4He ratios and the accuracy of 3Hec measurements, it is essential to understand what mechanism is responsible and under what conditions matrix helium loss is manifest. To address this question, olivines and pyroxenes with various amounts of matrix-sited 3He (from 107 to 1011 at. g−1) were crushed in air or in vacuum using several crushing devices. Sample temperature was controlled during each crushing experiment, and ranged from 25 to 325 °C. The resulting powders were then sieved to obtain several homogeneous grain fractions ranging between <10 and >300 μm. The 3Hec concentrations measured in each fraction clearly show that significant 3Hec loss (>20%) affects only the finest fraction (<10 μm) and, importantly, only under hot conditions (here T ?300 °C). Even the smallest fractions (<10 μm) quantitatively retain matrix-sited 3Hec when crushed under cold conditions (T ?25 °C), regardless of the duration and energy of crushing. These results invalidate the model previously proposed by (Yokochi R., Marty B., Pik R. and Burnard P. (2005) High 3He/4He ratios in peridotite xenoliths from SW Japan revisited: evidence for cosmogenic 3He released by vacuum crushing. Geochem. Geophys. Geosyst.6, doi:10.1029/2004GC000836) that involved spallation tracks and implied that the magnitude of loss was mainly controlled by the grain size. Moreover, new diffusion experiments were carried out to constrain the diffusivity of matrix-sited helium in crushed olivines. When used to model diffusive 3Hec loss as a function of grain size during crushing, these new data predict the observed release fairly well. Therefore, we conclude that temperature-enhanced volume diffusion is one of the main mechanisms controlling the release of 3Hec during crushing. For future applications, special attention should thus be paid to control the grain size, the crushing duration, and the temperature of the sample.  相似文献   

15.
The concentrations and behavior of oxygen and oxide ion were studied in silicate melts of composition CaO · MgO · xSiO2 (1.25 ≤ x ≤ 3) in the temperature range 1425 to 1575°C by cyclic voltammetry and chronopotentiometry. Electroreduction of oxygen is a reversible, 2 electron process involving dissociated oxygen atoms. The Henry's Law constant for O2 in molten diopside (CaO · MgO · 2SiO2) is 0.023 ± 0.004 mole/l atm at 1450°C. The diffusion coefficient for molecular oxygen in diopside melt is 4.5 ± .5 × 10?6 cm2/sec at 1450°C and the activation energy of diffusion is 80 ± 2 kcal/mole. Oxide ions produced by electroreduction of oxygen, rapidly dissociate silicate polymers, causing the concentration of free oxide ions in diopside melt to be buffered at a low level (4.7 ± .8 × 10?5 mole/l). The concentration of free oxide ion increases at higher proportions of metal oxides but remains at this value in more silicic melts. The rate of formation of oxide ions by polymerization in diopside melt is 0.021 ± .007 mole/l sec. Thermodynamic parameters (the standard free energy, enthalpy and entropy) for the oxidation of Ni, Co, and Zn in diopside melt in equilibrium with gaseous oxygen agree with those for solid oxide systems. The platinum reference electrode in molten diopside is a reversible, oxygen electrode.  相似文献   

16.
The validity of the thermodynamic cBΩ model is tested in terms of the experimentally determined diffusion coefficients of He in a natural Fe-bearing olivine (Fo90) and a synthetic end-member forsterite (Mg2SiO4) over a broad temperature range (250–950 °C), as reported recently by Cherniak and Watson (Geochem Cosmochim Acta 84:269–279, 2012). The calculated activation enthalpies for each of the three crystallographic axes were found to be (134 ± 5), (137 ± 13) and (158 ± 4) kJ mol?1 for the [100], [010] and [001] directions in forsterite, and (141 ± 9) kJ mol?1 for the [010] direction in olivine, exhibiting a deviation of <1 % with the corresponding reported experimental values. Additional point defect parameters such as activation volume, activation entropy and activation Gibbs free energy were calculated as a function of temperature. The estimated activation volumes (3.2–3.9 ± 0.3 cm3 mol?1) of He diffusion in olivine are comparable with other reported results for hydrogen and tracer diffusion of Mg cations in olivine. The pressure dependence of He diffusion coefficients was also determined, based on single experimental diffusion measurements at 2.6 and 2.7 GPa along the [001] direction in forsterite at 400 and 650 °C.  相似文献   

17.
Isotopic compositions of He (27 samples) and Ar (7 samples) as well as major and trace elements have been determined in Cenozoic effusive rocks and hosted olivine and pyroxene phenocrysts from northern and central Mongolia. The R = 3He/4He values are within (0.1–13)⋅10−6. Abnormally high R value, 13⋅10−6, atypical of Cenozoic basaltic-volcanism areas in Mongolia, has been first revealed at one of the sites of the Hangayn upland. In composition the rocks under study correspond to tephrites, trachybasalts, and subalkalic andesite-basalts. Analysis of their REE patterns and spidergrams shows that the elements participating in the formation of basalt fields of the Hangayn upland were supplied from the enriched mantle (EM1). These patterns are similar to the OIB ones; (La/Yb)n = 9–53. The R values in the olivine phenocrysts are higher as compared with the pyroxene phenocrysts and the bulk rock compositions of the same samples. Based on the elemental composition of the rocks, their contents of radiogenic 4He and 3He were calculated. The rate of 3He formation is 5.65⋅10−2 at/(g⋅year). The calculated and measured R values in the rock samples point to the presence of trapped mantle helium.  相似文献   

18.
We present new helium isotope data from the Macdonald seamount (Austral chain). The helium isotopic ratio varies from 4He/3He=45 000 (R/Ra=16.0) to 200 170 (R/Ra=3.6). The helium content is between 1.5×10?8 and 1.1×10?5 ccSTP/g. These helium results show clearly the presence of primitive mantle material in the source of the Austral chain. Macdonald has the lowest 4He/3He ratio among the Polynesian submarine volcanoes, except Hawaii (Loihi). The simplest explanation for the primitive helium signature is the presence under Macdonald of a mantle plume that derives either from the 670 km or 2900 km boundary layers, or, eventually, from the top of a large mantle dome resulting from a stratified two-layer convection. This plume contains less-degassed material with low 4He/3He ratio. To cite this article: M. Moreira, C. Allègre, C. R. Geoscience 336 (2004).  相似文献   

19.
The diffusivity of oxygen has been measured in three basaltic liquids from 1280 to 1450°C and 4 to 21 kilobars using a solid media piston-cylinder apparatus. The measurements were done by monitoring the reduction of ferric iron in previously oxidized spheres of basalt melt. The compositions studied were olivine nephelinite, alkali basalt, and 1921 Kilauea tholeiite.The isobaric temperature dependence of oxygen diffusivity is adequately described by Arrhenius relationships for the three liquids studied. Arrhenius activation energies were determined at 12 kilobars for olivine nephelinite (62± 6 kcal/mole) and tholeiite (51 ± 4 kcal/mole) and at 4, 12, and 20 kilobars for alkali basalt (70 ± 7, 86 ± 6, and 71 ± 14 kcal/mole, respectively). The Arrhenius parameters for the three compositions define a compensation law which is indistinguishable from those for oxygen diffusion in simple silicate melts (DUNN, 1982) and for divalent cation diffusion in basaltic melts (Hofmann, 1980). These results suggest that the principal species contributing to the total diffusivity of oxygen is the oxide anion (O2?).The isothermal pressure dependence of oxygen diffusion is complex and quite different from that observed for cationic diffusion in silicate melts. All three compositions show a sharp decrease in oxygen diffusivity at approximately the same pressure as the change in the liquidus phase from olivine to pyroxene, but otherwise the pressure dependence can be described by Arrhenius type equations. The equations yield negative activation volumes for the olivine nehpelinite and the alkali basalt. The activation volumes determined for the tholeiite are near zero at low pressure and positive at high pressure. A negative activation volume represents a decrease in the average size of the principal diffusing species.The results of this study are consistent with a melt model which includes both continuous changes in the relative proportions of the various anionic species in the melt with pressure and the occurrence of anionic disproportionation reactions within narrow pressure ranges.  相似文献   

20.
We document the first occurrence of Fe‐rich olivine‐bearing migmatitic metapelite in the Khondalite Belt, North China Craton. Petrological analyses revealed two exotic assemblages of orthopyroxene+spinel+olivine and orthopyroxene+spinel+cordierite. Phase relation modelling suggests that these assemblages are diagnostic of ultra‐high temperature (UHT) metamorphism in the Fe‐rich system, with temperatures from 1,000 to 1,050°C at 0.6 GPa. U–Th–Pb SIMS analyses on zircon reveal a similar age of c. 1.92 Ga for the olivine‐bearing migmatite and an adjacent gabbronoritic intrusion that is therefore identified as the heat source for the UHT metamorphism. These results, coupled with additional analysis of the famous Tuguiwula sapphirine‐bearing granulite, lead to a re‐appraisal of the P–T path shape and heat source for the UHT metamorphism. We suggest that UHT metamorphism, dated between 1.92 and 1.88 Ga, across the whole Khondalite belt, proceeded from a clockwise P–T evolution with an initial near‐isobaric heating path at ~0.6–0.8 GPa, and a maximum temperature of 1,050°C followed by a cooling path with minor decompression to ~0.5 GPa. Considering our results and previous works, we propose that the orogenic crust underwent partial melting at temperature reaching 850°C and depth of ~20 to ~30 km during a period of c. 30 Ma, between 1.93 and 1.90 Ga. During this time span, the partially molten crust was continuously intruded by mafic magma pulses responsible for local greater heat supply and UHT metamorphism above 1,000°C. We propose that the UHT metamorphism in the Khondalite belt is not related to an extensional post‐collisional event, but is rather syn‐orogenic and associated with mafic magma supplies.  相似文献   

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