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1.
Lattice preferred orientations (LPO) developed in perovskite and post-perovskite structured CaIrO3 were studied using the radial X-ray diffraction technique combined with a diamond anvil cell. Starting materials of each phase were deformed from 0.1 MPa to 6 GPa at room temperature. Only weak LPO was formed in the perovskite phase, whereas strong LPO was formed in the post-perovskite phase with an alignment of the (010) plane perpendicular to the compression axis. The present result suggests that the (010) is a dominant slip plane in the post-perovskite phase and it is in good agreement with the crystallographic prediction, dislocation observations via transmission electron microscopy, and a recent result of simple shear deformation experiment at 1 GPa–1,173 K. However, the present result contrasts markedly from the results on MgGeO3 and (Mg,Fe)SiO3, which suggested that the (100) or (110) is a dominant slip plane with respect to the post-perovskite structure. Therefore it is difficult to discuss the behavior of the post-perovskite phase in the Earth’s deep interior based on existing data of MgGeO3, (Mg,Fe)SiO3 and CaIrO3. The possible sources of the differences between MgGeO3, (Mg,Fe)SiO3 and CaIrO3 are discussed.  相似文献   

2.
Raman spectroscopy and heat capacity measurements have been used to study the post-perovskite phase of CaIr0.5Pt0.5O3, recovered from synthesis at a pressure of 15 GPa. Laser heating CaIr0.5Pt0.5O3 to 1,900 K at 60 GPa produces a new perovskite phase which is not recoverable and reverts to the post-perovskite polymorph between 20 and 9 GPa on decompression. This implies that Pt-rich CaIr1−xPtxO3 perovskites including the end member CaPtO3 cannot easily be recovered to ambient pressure from high P–T synthesis. We estimate an increase in the thermodynamic Grüneisen parameter across the post-perovskite to perovskite transition of 34%, of similar magnitude to those for (Mg,Fe)SiO3 and MgGeO3, suggesting that CaIr0.5Pt0.5O3 is a promising analogue for experimental studies of the competition in energetics between perovskite and post-perovskite phases of magnesium silicates in Earth’s lowermost mantle. Low-temperature heat capacity measurements show that CaIrO3 has a significant Sommerfeld coefficient of 11.7 mJ/mol K2 and an entropy change of only 1.1% of Rln2 at the 108 K Curie transition, consistent with the near-itinerant electron magnetism. Heat capacity results for post-perovskite CaIr0.5Rh0.5O3 are also reported.  相似文献   

3.
The evolution of the distortion of MgGeO3 enstatite and CaGeO3 wollastonite with increasing pressure, has been investigated using X-ray absorption spectroscopy (XAS) in a diamond anvil cell. At room temperature and low pressure (P<7 GPa), the compressibility of the GeO4 tetrahedron is higher in MgGeO3 enstatite (K [GeO4]∼135 GPa) than in CaGeO3 wollastonite (K [GeO4]≥ 280 GPa). The compression mechanisms of the two compounds are different: the whole mineral compressibility of Ge-enstatite appears to be very homogeneous, in contrast to that of Ge-wollastonite which exhibits an inhomogeneous tretrahedral compressibility. This result is consistent with the variation of the Debye-Waller factors of the two compounds with increasing pressure. At higher pressures, the coordination of germanium atoms in the two compounds gradually changes from fourfold to sixfold. For CaGeO3 the coordination change starts at 7 GPa and is complete a 12 GPa, whereas it starts at about 8.5 GPa for MgGeO3 and is not complete at 31 GPa. The progressive evolution of the measured Ge-O distances as well as the modification in the X-ray absorption near-edge structure indicate two coexisting different sites rather than a progressive site modification. The transformation is found to be partially reversible in CaGeO3 wollastonite, whereas it is totally reversible in MgGeO3 enstatite.  相似文献   

4.
Structural, morphological, magnetic, and thermal properties have been investigated for a novel post-perovskite oxide CaPtO3 synthesized under high pressure. By comparing obtained structural parameters with those for known post-perovskite compounds, we argue that the chemical bond has a strong covalent character. Precise measurements of the Langevin susceptibility χ 0 = −9.6 × 10−5 emu/mol and Debye temperature θ ∼ 470 K provide a good opportunity to confirm the reliability of first-principle calculations on predicting physical properties of the Earth’s D” layer.  相似文献   

5.
Bridgmanite (Mg,Fe)SiO3 and ferropericlase (Mg,Fe)O are the most abundant phases in the lower mantle and localized regions of the D″ layer just above the core mantle boundary. Seismic anisotropy is observed near subduction zones at the top of the lower mantle and in the D″ region. One source of anisotropy is dislocation glide and associated texture (crystallographic preferred orientation) development. Thus, in order to interpret seismic anisotropy, it is important to understand texture development and slip system activities in bridgmanite and bridgmanite + ferropericlase aggregates. Here we report on in situ texture development in bridgmanite and bridgmanite + ferropericlase aggregates deformed in the diamond anvil cell up to 61 GPa. When bridgmanite is synthesized from enstatite, it exhibits a strong (4.2 m.r.d.) 001 transformation texture due to a structural relationship with the precursor enstatite phase. When bridgmanite + ferropericlase are synthesized from olivine or ringwoodite, bridgmanite exhibits a relatively weak 100 transformation texture (1.2 and 1.6 m.r.d., respectively). This is likely due to minimization of elastic strain energy as a result of Young’s modulus anisotropy. In bridgmanite, 001 deformation textures are observed at pressures <55 GPa. The 001 texture is likely due to slip on (001) planes in the [100], [010] and \(\left\langle {110} \right\rangle\) directions. Stress relaxation by laser annealing to 1500–1600 K does not result in a change in this texture type. However, at pressures >55 GPa a change in texture to a 100 maximum is observed, consistent with slip on the (100) plane. Ferropericlase, when deformed with bridgmanite, does not develop a coherent texture. This is likely due to strain heterogeneity within the softer ferropericlase grains. Thus, it is plausible that ferropericlase is not a significant source of anisotropy in the lower mantle.  相似文献   

6.
Determination of preferred orientations in sulphide ores is an important facet in the analysis of the deformation and metamorphism in ore deposits. The methodology and problems of texture determinations in deformed sulphides are briefly reviewed. Deformation mechanisms and texture development in the common sulphide minerals are summarised. Axi-symmetric experimental deformation of galena, sphalerite and chalcopyrite produces similar pole figures with the (110) planes aligned normal to the compression axis. Deformation textures in naturally deformed sulphides however are best preserved in monomineralic ores which have undergone simple shear deformation. These textures can be correlated with the microstructures found in the sulphides. Computer simulations of deformation textures arising from dislocation mechanisms can be used to interpret the textures but the results to date are preliminary. These theoretical models emphasize the importance of the symmetry of the kinematic axes of the deformation, the operative glide systems and the strain history and the deformation path. Little is known, however, of the influence of static and dynamic recrystallisation on sulphide preferred orientations.  相似文献   

7.
The Raman spectra of bixbyite, Mn2O3, were measured up to 40 GPa at room temperature. Mn2O3 undergoes a phase transition from the C-type rare earth structure to the CaIrO3-type (post-perovskite) structure at 16–25 GPa. The transition pressure measured in Raman spectroscopy is significantly lower than the pressure reported previously by an X-ray diffraction study. This could be due to the greater polarizability in the CaIrO3-type structure, consistent with high-pressure observation on the CaIrO3 type in MgGeO3, although it is still possible that experimental differences may cause the discrepancy. Unlike the change at the perovskite to CaIrO3-type transition, the spectroscopic Grüneisen parameter does not decrease at the C-type to CaIrO3-type transition. The spectroscopic Grüneisen parameter of the low-pressure phase (C type) is significantly lower than thermodynamic Grüneisen parameter, suggesting significant magnetic contributions to the thermodynamic property of this material. Our Raman measurements on CaIrO3-type Mn2O3 contribute to building systematic knowledge about this structure, which has emerged as one of the common structures found in geophysically important materials.  相似文献   

8.
 Calcium self-diffusion rates in natural calcite single crystals were experimentally determined at 700 to 900° C and 0.1 MPa in a stream of CO2. Diffusion coefficients (D) were determined from 42Ca concentration profiles measured with an ion microprobe. The Arrhenius parameters yield an activation energy (Q)=382±37 kJ/mol and pre-exponential factor (D0)=0.13 m2/s, and there is no measurable anisotropy. Calcium grain boundary diffusion rates were experimentally determined in natural (Solnhofen) limestone and hot-pressed calcite aggregates at 650° to 850° C and 0.1 to 100 MPa pressure. The Solnhofen limestone was first pre-annealed for 24 h at 700° C and 100 MPa confining pressure under anhydrous conditions to produce an equilibrium microstructure for the diffusion experiments. Values for the product of the grain boundary diffusion coefficient (D′) and the effective grain boundary diffusion width (δ) were determined from 42Ca concentration profiles measured with an ion microprobe. The results show that there is no measurable difference between D′δ values obtained for pre-annealed Solnhofen samples at 0.1 and 100 MPa or between hot-pressed calcite aggregates and pre-annealed Solnhofen samples. The temperature dependence for calcium grain boundary diffusion in Solnhofen samples annealed at 0.1 MPa is described by the Arrhenius parameters D′ 0δ=1.5×10−9 m3/s and Q=267±47 kJ/mol. Comparison of the results of this study with previously published data show that calcium is the slowest volume diffusing species in calcite. The calcium diffusivities measured in this study place constraints on several geological processes that involve diffusive mass transfer including diffusion-accommodated mechanisms in the deformation of calcite rocks. Received: 19 December 1994/Accepted: 30 June 1995  相似文献   

9.
Fluid inclusions in quartz are known to modify their shapes and microstructures (textures) during weak plastic deformation. However, such changes have not been experimentally demonstrated and criteria are not available to relate them to paleostress conditions. To address these issues, quartz crystals containing natural CO2–H2O–NaCl fluid inclusions have been experimentally subjected to compressive deviatoric stresses of 90–250 MPa at 700°C and ~600 MPa confining pressure. Strains of up to 1% cause the inclusions to develop irregular shapes and to generate microcracks in crystallographic planes oriented subperpendicular to the major compression axis, σ 1. The uniform alignment of the microcracks imparts a planar fabric to the samples. The microcracks heal and form swarms of tiny satellite inclusions. These new inclusions lose H2O by diffusion, thereby triggering plastic deformation of the surrounding quartz via H2O-weakening. Consequently, the quartz samples deform plastically only in domains originally rich in inclusions. This study shows that fluid inclusions deformed by deviatoric stresses may indeed record information on paleostress orientations and that they play a key role in facilitating crystal-plastic deformation of quartz.  相似文献   

10.
Dehydration kinetics of muscovite by in situ infrared microspectroscopy   总被引：2，自引：0，他引：2  
Dehydration behavior of muscovite flake was investigated at 760–860°C by using in situ high-temperature IR microspectroscopy for the OH absorption band around 3,620 cm−1. Isothermal kinetic heating experiments at each temperature gave detailed decrease curves of the OH band area with time. These curves have been simulated by the first and second order reactions or mono- and two-dimensional diffusion processes. The mono-dimensional diffusion was found to give the best fit to the experimental data and apparent diffusion coefficients D were determined at 760–860°C with the activation energy of 290 ± 20 kJ/mol. The apparent diffusion coefficients D varied with the sample thickness L. This variation can be explained by an m layers model with a unit length of L′ with a constant diffusion coefficient D′. Therefore, the dehydration process might be rate-limited by mono-dimensional diffusion through tetrahedral silicate sheet perpendicular to (001) planes of muscovite with a unit length of L′.  相似文献   

11.
A polycrystalline aggregate of anhydrite was deformed in torsion to a maximum shear strain of 8.1 at 700°C and a maximum shear strain rate of 5᎒-3 s-1. The crystallographic preferred orientation (CPO or texture) was investigated as a function of shear strain/shear strain rate in a radial profile from the centre to the edge of the sample. A deformation texture developed at shear strains of 1.5-2 (corresponding to shear strain rates of 1 to 1.3᎒-3 s-1) and reached a stable position relative to the kinematic frame at a shear strain of 3.7 (2.3᎒-3 s-1). Further shear strain only led to a small increase in texture strength but no change in the orientation relative to the kinematic frame. The CPO is very similar to naturally observed textures and can be explained by the activity of the {001}<010> and {012}<121> slip systems. Although independent mechanical data indicate that a change of mechanism from dislocation- to diffusion-controlled creep occurred at a shear strain of approximately 1.5, the texture does not weaken, but rather increases, in strength with higher shear strains.  相似文献   

12.
The structural compression mechanism and compressibility of diaspore, AlO(OH), were investigated by in situ single-crystal synchrotron X-ray diffraction at pressures up to 7 GPa using the diamond-anvil cell technique. Complementary density functional theory based model calculations at pressures up to 40 GPa revealed additional information on the pressure-dependence of the hydrogen-bond geometry and the vibrational properties of diaspore. A fit of a second-order Birch–Murnaghan equation of state to the p–V data resulted in the bulk modulus B 0 = 150(3) GPa and B 0 = 150.9(4) GPa for the experimental and theoretical data, respectively, while a fit of a third-order Birch–Murnaghan equation of state resulted in B 0 = 143.7(9) GPa with its pressure derivative B′ = 4.4(6) for the theoretical data. The compression is anisotropic, with the a-axis being most compressible. The compression of the crystal structure proceeds mainly by bond shortening, and particularly by compression of the hydrogen bond, which crosses the channels of the crystal structure in the (001) plane, in a direction nearly parallel to the a-axis, and hence is responsible for the pronounced compression of this axis. While the hydrogen bond strength increases with pressure, a symmetrisation is not reached in the investigated pressure range up to 40 GPa and does not seem likely to occur in diaspore even at higher pressures. The stretching frequencies of the O–H bond decrease approximately linearly with increasing pressure, and therefore also with increasing O–H bond length and decreasing hydrogen bond length. Electronic Supplementary Material The online version of this article () contains supplementary material, which is available to authorized users.  相似文献   

13.
The growth rates of albite and pyroxene (enstatite + diopside + spinel) reaction rims were measured at 1000°C and ˜700 MPa and found to be parabolic indicating diffusion-controlled growth. The parabolic rate constants for the pyroxene (+ spinel) rims in samples with 0.5 wt% H2O added or initially vacuum dried at 25°C and 250°C are 1.68 ± 0.09, 0.54 ± 0.05 and 0.25 ± 0.06 μm2/h, respectively. The values for albite rim growth in samples initially dried at 60°C and with 0.1 wt% H2O added are 0.25 ± 0.04 and 0.33 ± 0.03 μm2/h, respectively. The latter values were used to derive the product of the grain boundary diffusion coefficient D′A, where A = SiO2, NaAlO2, or NaAlSi−1, and the grain boundary thickness δ in albite. The calculated D′SIO2δ in the albite aggregate for the situations of two different water contents are about 9.9 × 10−23 and 1.4 × 10−22 m3 s−1, respectively. Both the rate constants and the calculated D′Aδ demonstrate that the effect of water content on the grain boundary diffusion rate in monomineralic albite and polymineralic pyroxene (+ spinel) aggregates is small, consistent with recent studies of monomineralic enstatite and forsterite rims. Received: 1 July 1995 / Accepted: 1 August 1996  相似文献   

14.
The equation of state of MgGeO3 perovskite was determined between 25 and 66 GPa using synchrotron X-ray diffraction with the laser-heated diamond anvil cell. The data were fit to a third-order Birch–Murnaghan equation of state and yielded a zero-pressure volume (V 0) of 182.2 ± 0.3 Å3 and bulk modulus (K 0) of 229 ± 3 GPa, with the pressure derivative (K′0 = (?K 0/?P) T ) fixed at 3.7. Differential stresses were evaluated using lattice strain theory and found to be typically less than about 1.5 GPa. Theoretical calculations were also carried out using density functional theory from 0 to 205 GPa. The equation of state parameters from theory (V 0 = 180.2 Å3, K 0 = 221.3 GPa, and K′0 = 3.90) are in agreement with experiment, although theoretically calculated volumes are systematically lower than experiment. The properties of the perovskite phase were compared to MgGeO3 post-perovskite phase near the observed phase transition pressure (～65 GPa). Across the transition, the density increased by 2.0(0.7)%. This is in excellent agreement with the theoretically determined density change of 1.9%; however both values are larger than those for the (Mg,Fe)SiO3 phase transition. The bulk sound velocity change across the transition is small and is likely to be negative [?0.5(1.6)% from experiment and ?1.2% from theory]. These results are similar to previous findings for the (Mg,Fe)SiO3 system. A linearized Birch–Murnaghan equation of state fit to each axis yielded zero-pressure compressibilities of 0.0022, 0.0009, and 0.0016 GPa?1 for the a, b, and c axis, respectively. Magnesium germanate appears to be a good analog system for studying the properties of the perovskite and post-perovskite phases in silicates.  相似文献   

15.
 An in situ high-pressure (HP) X-ray diffraction investigation of synthetic diopside and of the Ca0.8Mg1.2Si2O6 clinopyroxene (Di80En20) was performed up to respectively P=40.8 and 15.1 GPa, using high brilliance synchrotron radiation. The compression of the cell parameters is markedly anisotropic, with βb ⋙ βc > βa > βasinβ for any pressure range and for both diopside and Di80En20. The compressibility along the crystallographic axes decreases significantly with pressure and is higher in Di80En20 than in diopside. The β cell parameter decreases as well with pressure, at a higher rate in Di80En20. The cell volume decreases at almost the same rate for the two compositions, since in diopside a higher compression along a* occurs. A change in the mechanism of deformation at P higher than about 5–10 GPa is suggested for both compositions from the analysis of the strain induced by compression. In diopside at lower pressures, the deformation mainly occurs, at a similar rate, along the b axis and at a direction 145° from the c axis on the (0 1 0) plane. At higher pressures, instead, the deformation occurs mostly along the b axis. In Di80En20 the orientation of the strain axes is the same as in diopside. The substitution of Ca with Mg in the M2 site induces at a given pressure a higher deformation on (0 1 0) with respect to diopside, but a similar change in the compressional behaviour is found. Changes in the M2 polyhedron with pressure can explain the above compressional behaviour. A third-order Birch-Murnaghan equation of state was fit to the retrieved volumes, with K=105.1(9) GPa, K′=6.8(1) for diopside and K=107.3(1.4) GPa, K′=5.7(3) for Di80En20; the same equation can be applied for any pressure range. The elasticity of diopside is therefore not significantly affected by Mg substitution into the M2 site, in contrast to the significant stiffening occurring for Ca substitution into Mg-rich orthopyroxenes. Received: 3 January 2000 / Accepted: 21 May 2000  相似文献   

16.
Microfabrics were analysed in calcite mylonites from the rim of the Pelvoux massif (Western Alps, France). WNW-directed emplacement of the internal Penninic units onto the Dauphinois domain produced intense deformation of an Eocene-age nummulitic limestone under lower anchizone metamorphic conditions (slightly below 300 °C). Two types of microfabrics developed primarily by dislocation creep accompanied by dynamic recrystallisation in the absence of twinning. Coaxial kinematics are inferred for samples exhibiting grain shape fabrics and textures with orthorhombic symmetry. Their texture (crystallographic preferred orientation, CPO) is characterised by two c-axis maxima, symmetrically oriented at 15° from the normal to the macroscopic foliation. Non-coaxial deformation is evident in samples with monoclinic shape fabrics and textures characterised by a single oblique c-axis maximum tilted with the sense of shear by about 15°. From the analysis of suitably oriented slip systems for the main texture components under given kinematics it is inferred that the orthorhombic textures, which developed in coaxial kinematics, favour activity of <10–11> and <02–21> slip along the f and r planes, respectively, with minor contributions of basal-<a> slip. In contrast, the monoclinic textures, which developed during simple shear, are most suited for duplex <a> slip along the basal plane. The transition between the dominating slip systems for the orthorhombic and monoclinic microfabrics is interpreted to be due to the effects of dynamic recrystallisation upon texture development. Since oblique c-axis maxima documented in the literature are most often rotated not with but against the shear sense, calcite textures alone should not be used as unequivocal shear sense indicators, but need to be complemented by microstructural criteria such as shape preferred orientations, grain size estimates and amount of twinning.  相似文献   

17.
Atomic-scale mechanisms of plastic deformation in orthoenstatite, MgSiO3 are studied by computer simulation methods. The combined use of metadynamics and molecular dynamics allows a direct observation of the structural changes during the creation of stacking faults in the (100) plane. A sequence of slip deformations in two different (100) planes at P = 15 GPa and T = 1,000 K reveals a probable transformation mechanism for the ortho- to high-pressure clinopyroxene transition. Each of the observed slips consists of at least four partial deformations crossing high-energy intermediate structures. In agreement with experimental studies, both (100)[010] and (100)[001] slip systems are activated in the deformation process. The observation of a dominant (100)[001] single slip system in pyroxenes may be related to the fact that high-energy intermediate dislocations with (100)[010] component are not stable on geological or experimental timescales.  相似文献   

18.
The growth curve of the continental crust shows that large amounts of continental crust formed in the early part of the Earth history are missing. In order to test a hypothesis that the former crust was subducted to the deep mantle, we performed phase assemblage analysis in the systems of mid-oceanic ridge basalt (MORB), anorthosite, and tonalite–trondhjemite–granite (TTG) down to the core–mantle boundary (CMB) conditions. Results show that all these materials can be subducted to the CMB leading to the development of a compositional layering in the D″ layer. We speculate that there could be five layers of FeO-enriched melt from partial melting of MORB, MORB crust, anorthosite, TTG, and slab or mantle peridotite in ascending order. Although the polymorphic transformation of perovskite to post-perovskite in (Mg,Fe)SiO3 may explain the seismic discontinuity at the top of the D″ layer (D″ discontinuity), the effects of solid solution on the sharpness of the transformation suggest that the compositional layering is more plausible for the origin of the D″ discontinuity. The D″ layer can be an “anti-crust” made up mostly of TTG + anorthosite derived from the former continental crust. Tectonic style of the anti-crust at the CMB is similar to that at the surface. At both places, chemically distinct layers are density stratified and are also characterized by the processes of accretion, magmatism, and metasomatism.  相似文献   

19.
孙岩  琚宜文  黄骋  周巍  晁洪太  王志才 《地球科学》2018,43(5):1518-1523
通常认为岩石是被剪破或张裂的,那么,为何我们能寻觅到位于同压力垂直方向的破裂构造呢?H Odé剪切变形理论给出一个精辟的回答:在塑性或粘-弹性变形中,由于介质的分异作用,存在一个从屈服条件中获得的速度不连续性,这样,其介质就能沿着等速的特征面剪切滑移.该理论亦称为塑性剪切作用准则,之前是从宏观-直观力学表象予以验证,如构造挤压带的破裂面、正压力下Griffith裂隙端点裂开和垂直压力下的碎裂流动等.进而,我们对花岗岩标本实施高温/高压实验,并取其位于轴压垂直方向裂隙的薄壳表层做扫描电镜观测.然后把从其表层观察的具有H Odé力学表象的微纳米现象,同一般剪切作用的屈服效应结构,从3个方面相比较鉴别.（1）粘-弹性变形:高温-高压的实验样品更容易产生塑性压缩容积流动,不仅具粘性也具弹性变形,随之,样品可展现纳米涂层作用和纳米分层作用.（2）纳米尺度结构:纳米尺度颗粒能成为单一纳米粒-纳米线-纳米层结构,且复体的纳米粒可细分成粒状的、线状的和片粒状的结构等.（3）有序组构:尽管H Odé破裂的粒化流动和纹理流动的优选方位,同普通剪切作用相比,处于弱势范畴,然而综合分析观之,这两者的屈服特征是完全一致的.反之,我们应用H Odé剪切理论去研究一些非常规的变形现象,必能拓展纳米地质学的研讨范畴和认知能力.   相似文献   

20.
 Grain boundary diffusion rates of oxygen, potassium and calcium in fine-grained feldspar aggregates were determined experimentally. The starting materials were a natural albite rock from the Tanco pegmatite and aggregates hot-pressed from fragments of Amelia albite or Ab, Or and An composition glasses. The technique employed isotopic tracers (18O, 41K, 42Ca) either evaporated onto the surface or in an aqueous solution surrounding the sample, and depth profiling using an ion microprobe (SIMS). From the depth profiles, the product of the grain boundary diffusion coefficient (D′) and effective boundary width (δ) was calculated using numerical solutions to the appropriate diffusion equation. The experimental reproducibility of D′δ is a factor of 3. A separate determination of D′ independent of δ yields an effective grain boundary width of ∼3 nm, consistent with high resolution TEM observations of a physical grain boundary width <5 nm. Oxygen (as molecular water) grain boundary diffusion rates were determined in the Ab and Or aggregates at 450°–800° C and 100 MPa (hydrothermal), potassium rates in Or aggregates at 450°–700° C both at 0.1 MPa (in air) and at 100 MPa (hydrothermal), and calcium rates in An aggregates at 700°–1100° C and 0.1 MPa (in air). Oxygen grain boundary diffusion rates are similar in all three of the Ab aggregates and in the Or aggregate. Potassium and oxygen depth profiles measured in the same samples yield different D′δ values, confirming a diffusional transport mechanism. Potassium diffusion in the Or aggregate has a greater activation energy (216 vs 78 kJ/mol) than oxygen, and the Arrhenius relations cross at ∼625° C. Potassium D′δ values in Or aggregates are about a factor of five greater in hydrothermal experiments at 100 MPa than in experiments at 0.1 MPa in air. Calcium grain boundary diffusion rates in An aggregates are 4 to 5 orders of magnitude slower than potassium in Or and have a greater (291 kJ/mol) activation energy. This suggests that differences in formal charge and/or size of diffusing species may play an important role in their relative grain boundary diffusion rates. Received: 24 December 1993 / Accepted: 16 June 1994  相似文献   

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