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1.
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   

2.
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3.
The evolution with pressure of the unit-cell parameters brownmillerite (Ca2Fe2O5), a stoichiometric defect perovskite structure, has been determined to a maximum pressure of 9.46 GPa, by single-crystal X-ray diffraction measurements at room temperature. Brownmillerite does not exhibit any phase transitions in this pressure range. A fit of a third-order Birch–Murnaghan equation-of-state to the P–V data yields values of KT0=127.0(5) GPa and K0′=5.99(13). Analysis of the unit-cell parameter data shows that the structure compresses anisotropically. Compressional moduli for the axes are Ka0=141(1) GPa, Kb0=118(3) GPa and Kc0=122.2(2) GPa, with Ka0′=8.9(3), Kb0′=6.2(6) and Kc0′=4. The stiffest direction (i.e. along a) coincides with the direction of the FeO4 tetrahedral chains. Comparison of these data with the elasticity systematics of Ca-perovskites shows that the presence of oxygen vacancies in the brownmillerite structure softens the structure by ∼25% and that the ordering of vacancies in the perovskite structure increases the anisotropy of compression.  相似文献   

4.
The aggregate shear wave velocities of MgO (periclase) have been determined throughout Earth's lower mantle pressure regime approaching 130 GPa using Brillouin spectroscopy in conjunction with synchrotron X-ray diffraction technique in a diamond anvil cell apparatus. We found that the extrapolations of the high-pressure shear wave velocities and shear moduli to ambient pressure are highly consistent with earlier studies. However, the measurements over a wide pressure range revealed that the pressure derivative of the shear modulus (dG/dP = G0′) of MgO is 1.92(2), which is distinctly lower than that of previous lower-pressure experiments. Compared with the previous results on (Mg,Fe)O ferropericlase, there is no clear correlation between iron content and G0′. We calculate that the shear wave velocity profile of lower mantle along the adiabatic geotherm applied by the lower G0′ value of periclase can remarkably well reproduce the global seismological 1-D velocity profile model with uniform composition model. The best-fitting result indicates the possibility of a lower mantle mineralogy with ~ 92 vol.% silicate perovskite phase, implying that the bulk composition of lower mantle is likely not to be pyrolitic but more chondritic. The present acoustic measurements performed over the large pressure range have thus led us to a better understanding of compositional model of the Earth's lower mantle.  相似文献   

5.
In the central Western Alps, a combined structural, petrological and 40Ar–39Ar geochronological study of the Modane-Aussois and Southern Vanoise units yields important constraints on the timing of deformation and exhumation of the Briançonnais zone. These data help to decipher the respective roles of oceanic subduction, continental subduction and collision in the burial and exhumation of the main units through time. In the Modane-Aussois unit top to the NW thrusting (D1) was followed by top to the east shearing (D2) interpreted by some as normal faulting and by others as backthrusting. Pseudosection calculations imply that D1 deformation occurred at 1.0 ± 0.1 GPa and 350 ± 30 °C. Analysis of chlorite–phengite pairs yield P–T estimates between 0.15 and 0.65 GPa and between 220 and 350 °C for the D2 event. Phengites along the D1 schistosity (sample M80) yields an 40Ar–39Ar age of 37.12 ± 0.39 Ma, while D2 phengites yield ages of 35.42 ± 0.38 (sample M173) and 31.60 ± 0.33 Ma (sample M196). It was not possible to test whether these ages are altered by excess argon or not. Our interpretation is that the D1/D2 transition occurred at ∼37 Ma at the beginning of decompression, and that D2 lasted until at least ∼32 Ma. Pseudosection calculation suggests that the Southern Vanoise unit was buried at 1.6 ± 0.2 GPa and 500–540 °C. D1 deformation occurred during exhumation until 0.7–10.5 GPa and 370 ± 30 °C. Published ages suggest that D1 deformation possibly started at ∼50 Ma and lasted until ∼37 Ma. D2 deformations started at P–T conditions close to that recorded in Modane-Aussois unit and lasted until 0.2 ± 0.1 GPa and 280 ± 30 °C at ∼28 Ma. The gap of 0.6 ± 0.3 GPa and 150 ± 130 °C between peak metamorphic conditions in the two units was concealed by thrusting of the South Vanoise unit on top of the Modane-Aussois unit during D1 Deformation. Top to the east deformation (D2) affects both units and is interpreted as backthrusting.Based on these data, we propose a geodynamic reconstruction where the oceanic subduction of the Piedmont unit until ∼50 Ma, is followed by its exhumation at the time of continental subduction of the continental Southern Vanoise unit until ∼45 Ma. The Southern Vanoise is in turn underthrusted by the Modane-Aussois unit until ∼37 Ma (D1). Between 37 and 31 Ma the Modane-Aussois and Southern Vanoise units exhume together during backthrusting to the east (D2). This corresponds to the collision stage and to the activation of the Penninic Thrust. In the ∼50 Ma to ∼31 Ma time period the main thrusts propagated westward as the tectonic context switched from oceanic to continental subduction and finally to collision. During each stage, external units are buried while internal ones are exhumed.  相似文献   

6.
Single-crystal elasticity of stishovite was examined using a new experimental technique and an empirical macroscopic model. Employing high-frequency resonant ultrasound spectroscopy, single-crystal elastic constants of stishovite were determined: C11 = 443(3), C33 = 781(4), C12 = 193(2), C23 = 199(2), C44 = 256(2), and C33 = 316(2) GPa. The frequency range of the resonant ultrasound spectroscopy techniques was 6–20 MHz, which is much lower than the ～10 GHz range of the Brillouin scattering technique. Of the elastic constants, the shear elastic constants C44 and C66 are consistent with the average value of the previously mentioned Brillouin scattering. Conversely, the four elastic constants, C11, C33, C12, and C23, slightly deviate outside the range of previous Brillouin scattering results. The present results, except those for C12, are consistent with recent lattice dynamic analysis of inelastic X-ray scattering data. The adiabatic bulk modulus was calculated as 298 GPa, which is smaller and more consistent with the result of compression experiments than any other Brillouin scattering results (301–312 GPa). The present result shows greater P-wave velocity anisotropy (24.7%) than any preceding work. To understand the unique elastic properties of stishovite, the Gingham check model was proposed and examined. The result shows that the octahedron of 6-coordinated Si in stishovite crystal has stiffness comparable to that of diamond.  相似文献   

7.
《Continental Shelf Research》2006,26(17-18):2241-2259
The Amazon River spawns a vast mobile mudbelt extending ∼1600 km from the equator to the Orinoco delta. Deposits along the Amazon–Guianas coastline are characterized by some of the highest Corg remineralization rates reported for estuarine, deltaic, or shelf deposits, however, paradoxically, except where stabilized by mangroves or intertidal algal mats, they are usually suboxic and nonsulfidic. A combination of tides, wind-driven waves, and coastal currents forms massive fluid muds and mobile surface sediment layers ∼0.5–2 m thick which are dynamically refluxed and frequently reoxidized. Overall, the seabed functions as a periodically mixed batch reactor, efficiently remineralizing organic matter in a gigantic sedimentary incinerator of global importance. Amazon River material entering the head of this dynamic dispersal system carries an initial terrestrial sedimentary Corg loading of ∼ 0.7 mg C m−2 particle surface area. Total Corg loading is lowered to ∼ 0.2 mg C m−2 in the proximal delta topset, ∼60–70% of which remains of terrestrial origin. Loading decreases further to 0.12–0.14 mg C m−2 (∼60% terrestrial) in mudbanks ∼600 km downdrift along French Guiana, values comparable to those found in the oligotrophic deepsea. DOC/ΣCO2 ratios in pore waters of French Guiana mudbanks indicate that >90% of metabolized organic substrates are completely oxidized. Within the Amazon delta topset at the head of the dispersal system, both terrestrial and marine organic matter contribute substantially to early diagenetic remineralization, although reactive marine substrate dominates (∼60–70%). The conditional rate constant for terrestrial Corg in the delta topset is ∼0.2 a−1. As sedimentary Corg is depleted during transit, marine sources become virtually the exclusive substrate for remineralization except very near the mangrove shoreline. The δ13C and Δ14C values of pore water ΣCO2 in mudbanks demonstrate that the primary source of remineralized organic matter within ∼1 km of shore is a small quantity of bomb signature marine plankton (+80‰). Thus, fresh marine organic material is constantly entrained into mobile deposits and increasingly drives early diagenetic reactions along the transit path. Relatively refractory terrestrial Corg is lost more slowly but steadily during sedimentary refluxing and suboxic diagenesis. Amazon Fan deposits formed during low sea level stand largely bypassed this suboxic sedimentary incinerator and stored material with up to ∼3X the modern high stand inner shelf Corg load (Keil et al., 1997b. Proceedings of the Ocean Drilling Program, Scientific Results. Vol. 155. pp. 531–537). Sedimentary dynamics, including frequency and magnitude of remobilization, and the nature of dispersal systems are clearly key controls on diagenetic processes, biogeochemical cycling, and global C storage along the continental margins.  相似文献   

8.
We have determined the post-perovskite phase transition boundary in MgSiO3 in a wide temperature range from 1640 to 4380 K at 119–171 GPa on the basis of synchrotron X-ray diffraction measurements in-situ at high-pressure and -temperature in a laser-heated diamond-anvil cell (LHDAC). The results show a considerably high positive Clapeyron slope of + 13.3 ± 1.0 MPa/K and a transition temperature of about 3520 ± 70 K at the core–mantle boundary (CMB) pressure. The thermal structure in D″ layer can be tightly constrained from precisely determined post-perovskite phase transition boundary and the depths of paired seismic discontinuities. These suggest that temperature at the CMB may be around 3700 K, somewhat lower than previously thought. A minimum bound on the global heat flow from the core is estimated to be 6.6 ± 0.5 TW.  相似文献   

9.
The Piranshahr metaperidotites in the northwestern end of the Zagros orogen were emplaced following the closure of the Neotethys ocean. The ophiolitic rocks were emplaced onto the passive margin of the northern edge of the Arabian plate as a result of northeastward subduction and subsequent accretion of the continental fragments. The metaperidotites have compositions ranging from low-clinopyroxene lherzolite to harzburgite and dunite. They are mantle residues with distinct geochemical signatures of both mid-ocean ridge and supra subduction zone (SSZ) affinities. The abyssal peridotites are characterized by high Al2O3 and Cr2O3 contents and low Mg-number in pyroxenes. The Cr-number in the coexisting spinel is also low. The SSZ mantle peridotites are characterized by low Al2O3 contents in pyroxenes as well as low Al2O3 and high Cr-number in spinel. Mineral chemical data indicate that the MOR- and SSZ-type peridotites are the residues from ∼15–20% and ∼30–35% of mantle melting, respectively. Considering petrography, mineralogy and textural evidence, the petrological history of the Piranshahr metaperidotites can be interpreted in three stages: mantle stable stage, serpentinization and metamorphism. The temperature conditions in the mantle are estimated using the Ca-in-orthopyroxene thermometer as 1210 ± 26 °C. The rocks have experienced serpentinization. Based on the textural observations, olivine and pyroxene transformed into lizardite and/or chrysotile with pseudomorphic textures at temperatures below 300 °C during the initial stage of serpentinization. Subsequent orogenic metamorphism affected the rocks at temperatures lower than 600 °C under lower-amphibolite facies metamorphism.  相似文献   

10.
High-pressure phase relations in the system NaAl3Si3O11–CaAl4Si2O11 were examined at 13–23 GPa and 1600–1900 °C, using a multianvil apparatus. A Ca-aluminosilicate with CaAl4Si2O11 composition, designated CAS phase, is stable above about 13 GPa at 1600 °C. In the system NaAl3Si3O11–CaAl4Si2O11, the CAS phase dissolving NaAl3Si3O11 component coexists with jadeite, corundum and stishovite below 22 GPa, above which the CAS phase coexists with Na-rich calcium ferrite, corundum and stishovite. At 1600 °C, the solubility of NaAl3Si3O11 component in the CAS solid solution increases with increasing pressure up to about 50 mol% at about 22 GPa, above which the solubility decreases with pressure. The maximum solubility of NaAl3Si3O11 component in the CAS phase increases with temperature up to around 70 mol% at 1900 °C at 22 GPa. The dissociation of NaAlSi2O6 jadeite to NaAlSiO4 calcium ferrite plus stishovite occurs at about 22 GPa. Lattice parameters of the CAS phase with the hexagonal Ba-ferrite structure change with increase of the NaAl3Si3O11 component: a-axis decreases and c-axis slightly increases, resulting in decrease of molar volume. Enthalpies of the CAS solid solutions were measured by high-temperature drop-solution calorimetry techniques. The results show that enthalpy of hypothetical NaAl3Si3O11 CAS phase is much higher than the mixture of NaAlSi2O6 jadeite, corundum and stishovite and is close to that of the mixture of NaAlSiO4 calcium ferrite, corundum and stishovite. When we adopt the Na:Ca ratio of 75:25 of the natural Na-rich CAS phase in a shocked Martian meteorite, Zagami, the phase relations determined above suggest that the natural CAS phase crystallized from melt at pressure around 22 GPa and temperature close to or higher than 2000–2200 °C. The inferred P, T conditions are consistent with those estimated using other high-pressure minerals in the shocked meteorite.  相似文献   

11.
The Ca isotope compositions of 37 late Mesozoic skeletal carbonates, belemnites and brachiopods, from the Tethyan realm were analyzed by thermal (TIMS) and plasma (MC-ICP-MS) ionization mass spectrometry. A poor correlation between δ44/40Ca and δ18O values of belemnites suggests only a weak temperature dependency for the Ca isotope composition of belemnites, likely less than 0.02‰/°C. The δ44/40Ca record of belemnites was therefore used to reconstruct the Ca isotope composition of paleo-seawater (δ44/40CaSW), based on an experimentally determined fractionation factor between seawater Ca and belemnite calcite (αCC–SW) of ∼ 0.9986. The inferred δ44/40CaSW record, with an average stratigraphic resolution of 1 Ma, shows systematic temporal variation of ∼ 0.5‰ with the Middle/Late Jurassic (∼ 154 Ma) minimum of ∼ 1.4‰ and a subsequent general increase to the Early Cretaceous (∼ 124 Ma) maximum of ∼ 1.9‰. The global nature of the δ44/40CaSW record is supported by identical Ca isotope compositions of coeval (Kimmeridgian) belemnites collected from two distinct paleogeographic regions, the southern (New Zealand) and northern (Germany) margin of the Tethys Ocean. The observed late Mesozoic δ44/40CaSW record was simulated using a simple Ca isotope mass balance model, and the results indicate that the variation in δ44/40CaSW record can be explained by changes in oceanic input fluxes of Ca that were independent of the carbonate ion fluxes, such as the hydrothermal Ca flux or the release of Ca to the oceans via dolomitization of marine carbonates.  相似文献   

12.
The geochemical characteristics of mildly alkalic basalts (24–25 Ma) erupted in the southeastern Kerguelen Archipelago are considered to represent the best estimate for the composition of the enriched Kerguelen plume end-member. A recent study of picrites and high-MgO basalts from this part of the archipelago highlighted the Pb and Hf isotopic variations and suggested the presence of mantle heterogeneities within the Kerguelen plume itself. We present new helium and neon isotopic compositions for olivines from these picrites and high-MgO basalts (6–17 wt.% MgO) both to constrain the enriched composition of the Kerguelen plume and to determine the origin of isotopic heterogeneities involved in the genesis of Kerguelen plume-related basalts. The olivine phenocrysts have extremely variable 4He / 3He compositions between MORB and primitive values observed in OIB (∼90,000 to 40,000; i.e., R / Ra ∼8 to 18) and they show primitive neon isotopic ratios (average 21Ne / 21Neext ∼0.044). The neon isotopic systematics and the 4He / 3He ratios that are lower than MORB values for the Kerguelen basalts clearly suggest that the Kerguelen hotspot belongs to the family of primitive hotspots, such as Iceland and Hawaii. The rare gas signature for the Kerguelen samples, intermediate between MORB and solar, is apparently inconsistent with mixing of a primitive component with a MORB-like source, but may result from sampling a heterogeneous part of the mantle with solar 3He / 22Ne and with a higher (U, Th) / 3He ratio compared to typically high R / Ra hotspot basalts such as those from Iceland and Hawaii.  相似文献   

13.
The elastic moduli of polycrystalline ringwoodite, (Mg0.91Fe0.09)2SiO4, were measured up to 470 K by means of the resonant sphere technique. The adiabatic bulk (KS) and shear (μ) moduli were found to be 185.1(2) and 118.22(6) GPa at room temperature, and the average slopes of dKS/dT and dμ/dT in the temperature range of the study were determined to be −0.0193(9) and −0.0148(3) GPa/K, respectively. Using these results, we estimate seismic wave velocity jumps for a pure olivine mantle model at 520 km depth. We find that the jump for the S-wave velocity is about 1.5 times larger than that for the P-wave velocity at this depth. This suggests that velocity jumps at the 520 km discontinuity are easier to detect using S-waves than P-waves.  相似文献   

14.
Drinking water wells indiscriminatingly placed adjacent to fecal contaminated surface water represents a significant but difficult to quantify health risk. Here we seek to understand mechanisms that limit the contamination extent by scaling up bacterial transport results from the laboratory to the field in a well constrained setting. Three pulses of Escherichia coli originating during the early monsoon from a freshly excavated pond receiving latrine effluent in Bangladesh were monitored in 6 wells and modeled with a two-dimensional (2-D) flow and transport model conditioned with measured hydraulic heads. The modeling was performed assuming three different modes of interaction of E. coli with aquifer sands: (1) irreversible attachment only (best-fit ki = 7.6 day−1); (2) reversible attachment only (ka = 10.5 and kd = 0.2 day−1); and (3) a combination of reversible and irreversible modes of attachment (ka = 60, kd = 7.6, ki = 5.2 day−1). Only the third approach adequately reproduced the observed temporal and spatial distribution of E. coli, including a 4-log10 lateral removal distance of ∼9 m. In saturated column experiments, carried out using aquifer sand from the field site, a combination of reversible and irreversible attachment was also required to reproduce the observed breakthrough curves and E. coli retention profiles within the laboratory columns. Applying the laboratory-measured kinetic parameters to the 2-D calibrated flow model of the field site underestimates the observed 4-log10 lateral removal distance by less than a factor of two. This is promising for predicting field scale transport from laboratory experiments.  相似文献   

15.
Two late Mesozoic granitoids in the Luanchuan area of the East Qinling orogen are considered; ore-bearing rocks are granite porphyries and granodiorite, with K2O > Na2O, appearing in the form of stocks. The Laojunshan rocks contains dominantly monzonitic granite, with K2O ≈ Na2O, in the form of a batholith. Both the ore-bearing rocks and the Laojunshan rocks are highly siliceous and shoshonitic, high-K calc-alkaline, similar to some I-type granites. Light rare earth elements (LREEs) are enriched in both rock suites, although the Luanchuan ore-bearing granitoids have higher concentrations, with (La/Yb)N ratios twice that of the barren Laojunshan granite suite. Ore-bearing rocks have, therefore, undergone greater fractionation of heavy rare earth elements. All Laojunshan rocks have negative Eu anomalies, indicating plagioclase fractionation. δEu values are different in both rock suites, the values in the ore-bearing granites, ranging from 0.52 to 1.04, which are much higher than that of Laojunshan batholith, ranging from 0.4 to 0.65. (La/Sm)N values of ore-bearing granites are 5.32–8.28, while that of Laojunshan batholith are 3.75–5.77, confirming the observation that the ore-bearing granites have undergone a higher degree of strong differentiation than that of Lanjunshan batholith.Major and trace element data, and REE data, combined with isotope data from previous work and the close relationships between the tectonic settings of the barren and ore-bearing rocks indicate that both groups of rocks were derived from the lower crust. At ∼157 Ma, with the tectonic regime in transition from a syn-collisional to a post-collisional setting, highly fractionated granites ascended from their storage area via faults; at ∼145 Ma, ore-bearing plutons, which are triggered by slab melts, formed at the junctions of fault planes trending WNW-ESE and NE-SW. At ∼115 Ma, the tectonic regime changed from compression to extension; in this environment, the barren Laojunshan batholith was emplaced, representing the end of the collisional event.  相似文献   

16.
The mineralogy adopted by a depleted harzburgite composition has been studied over the pressure interval 5–26 GPa at temperatures of 1300–1400°C. The pyroxene-garnet component of the harzburgite composition (harzburgite minus 82 wt.% olivine) transforms to majorite garnet by 18–19 GPa, and further disproportionates to the assemblage of garnet + stishovite + Mg2SiO4 spinel above 20 GPa. At still higher pressures, first ilmenite (22–24 GPa) and then perovskite MgSiO3 (24–26 GPa) are found to coexist with garnet. Garnet disappears at 26 GPa and almost complete transition to perovskite is achieved at this pressure. The mineral proportions and density profiles in the subducting oceanic lithosphere, modelled by a combination of 80% harzburgite + 20% primitive MORB compositions are calculated as a function of depth under conditions isothermal with surrounding pyrolite mantle, and also for a temperature distribution in which the slab is substantially cooler than surrounding mantle to below 700 km. Under isothermal conditions, the slab has a density similar to surrounding mantle to a depth of 600 km. However, between 600 and 700 km, the slab is up to 0.08 g/cm3 denser than surrounding mantle. This is caused primarily by the higher alumina content in pyrolite as compared to harzburgite, which causes the transition to perovskite in pyrolite to occur at substantially higher pressures than in harzburgite. The presence of alumina also smears out the garnet-perovskite transition in pyrolite over a depth interval of 50 km, whereas this transformation is much sharper in the harzburgite composition. Calculations based on the observed phase equilibria also show that a subducted cool slab remains much denser (by 0.1–0.3 g/cm3) than surrounding mantle to a depth of 700 km but possesses a density similar to surrounding mantle below this depth. These results have important implications for the dynamical behaviour of slabs possessing different thermal regimes when they encounter the 670 km discontinuity and also for the nature of this discontinuity.  相似文献   

17.
We have studied the phase transformation of forsterite to wadsleyite under shear stress at the Earth's transition zone pressure and temperature conditions. Two-step experiments were performed using a multi-anvil press. First, we hot pressed iron-free forsterite at 6 or 11 GPa and 1100 °C. Then we deformed a slab of this starting material using a direct simple shear assembly at 16 GPa and 1400 °C for 1, 15, 35, 40, or 60 min. Both the starting material and the deformed samples were characterized using optical and scanning electron microscopy including measurements of crystal preferred orientations (CPO) by electron back scattered diffraction (EBSD), transmission electron microscopy (TEM), and Fourier transform infrared spectroscopy (FTIR). The phase transformation occurs very rapidly, in less than 1 min, and metastable forsterite relics are not observed after deformation. The grain size of wadsleyite is slightly smaller than the forsterite starting material. The water contents obtained from FTIR analyses in forsterite and wadsleyite are 65–124 wt ppm H2O and 114–736 wt ppm H2O, respectively, which are well below water solubility at similar conditions in the presence of free water. Wadsleyite aggregates display weak CPO patterns with [1 0 0] axes concentrated at low angle to the shear direction, [0 1 0] axes perpendicular to the shear plane and nearly random [0 0 1] axes. Only a few dislocations were observed in wadsleyite with TEM. This observation is consistent with the assumption that most dislocations formed during the initial high-stress stages of these stress-relaxation experiments, were consumed in the phase transformation, probably enhancing the transformation rate. CPO patterns vary as a function of the water content: with increasing water content the density of [1 0 0] axes parallel to the shear direction decreases, and the density of [0 0 1] axes increases. Viscoplastic self-consistent modeling of CPO evolution using previously reported glide systems for wadsleyite, i.e., [1 0 0]{0 k l} and 1/2 〈1 1 1〉{1 0 1}, cannot reproduce the measured CPO, unless the [0 0 1](0 1 0) system, for which dislocations have not been observed by TEM, is also activated. In addition, wadsleyite grain growth suggests the participation of diffusion-assisted processes in deformation. Calculated anisotropies for P and S-waves using measured CPO are always below 1%. This very low anisotropy is due to both the low finite strain achieved in the experiments, which leads to weak wadsleyite CPO, and to the diluting effect of added majorite. The present experiments emphasize the importance of stress, grain size evolution and water content in the forsterite to wadsleyite phase transformation and subsequent deformation in the transition zone.  相似文献   

18.
The high-pressure and temperature phase transformations of MgSiO3 have been investigated in a diamond-anvil cell coupled with laser heating from 150 to 300 kbar at 1000–1400°C. X-ray diffraction study of the quenched samples reveals that the sequence of phase transformations for this compound is clinoenstatite → β-Mg2SiO4 plus stishovite → Mg2SiO4(spinel) plus stishovite → ilmenite phase → perovskite phase with increasing pressure. The hexagonal form of MgSiO3 observed by Kawai et al. is demonstrated to have the ilmenite structure and the “hexagonal form” of MgSiO3 observed by Ming and Bassett is shown to be predominantly the orthorhombic perovskite phase plus the ilmenite phase. The mixture of oxides, periclase plus stishovite, reported by Ming and Bassett was not observed in this study. The very wide stability field for the ilmenite phase of MgSiO3 found in this study suggests that this phase is of importance in connection with the observed rapid increase of velocity in the transition zone of the earth's mantle. On the basis of the extremely dense-packed structure of the perovskite phase of MgSiO3, this phase should be the most important component for the lower mantle.  相似文献   

19.
The single-crystal elastic moduli of the ilmenite phase of MgSiO3 have been determined from Brillouin spectroscopy. They are: C11 = 472, C12 = 168, C33 = 382, C13 = 70, C44 = 106, C14 = ?27, C66 = 152 and C25 = ?24 in GPa. These elastic properties are consistent with a structural mechanical model where the silicon octahedra are very stiff under compression and shear. This latter property yields an unexpectedly high shear modulus for the magnesium silicate ilmenite as compared with analogue compounds. The further transformation to perovskite will probably be associated with a significant increase in elastic properties since the strong silicon polyhedra form a structural network in this phase. The transformation of spinel and stishovite to ilmenite is associated with a slight density increase and a slight decrease in acoustic velocities. This transformation will probably not produce a seismic discontinuity even if it does occur in the Earth's mantle.  相似文献   

20.
Aluminum incorporation into the high pressure polymorph of TiO2 with the structure of α-PbO2 has been studied from 10 to 20 GPa and 1300 °C by XRD, high-resolution 27Al MAS-NMR and TEM. Al-doped α-PbO2 type TiO2 can be recovered at atmospheric pressure. Al2O3 solubility in α-PbO2 type TiO2 increases with increasing the synthesis pressure. The α-PbO2 type TiO2 polymorph is able to incorporate up to 35 wt.% Al2O3 at 13.6 GPa and 1300 °C, being the substitution of Ti4+ by Al3+ on normal octahedral sites the mechanism of solubility. The transition to the higher pressure TiO2 polymorph with the ZrO2 baddeleyite structure, Akaogiite, has not been observed in the quenched samples at room pressure. The microstructure of the recovered sample synthesized at 16 GPa and 1300 °C points to the existence of a non-quenchable aluminum titanium oxide phase at these conditions.  相似文献   

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