Lattice preferred orientation in CaIrO<Subscript>3</Subscript> perovskite and post-perovskite formed by plastic deformation under pressure     

Ken Niwa  Takehiko Yagi  Kenya Ohgushi  Sébastien Merkel  Nobuyoshi Miyajima  Takumi Kikegawa 《Physics and Chemistry of Minerals》2007,34(9):679-686

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   

Calibration of the superconducting gravimeter T011 by parallel observation with the absolute gravimeter FG5 #210—a Bayesian approach     

Yuichi Imanishi  Toshihiro Higashi  Yoichi Fukuda 《Geophysical Journal International》2002,151(3):867-878

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Study on Al2O3 content and phase stability of aluminous-CaSiO3 perovskite at high pressure and temperature     

N. Takafuji  T. Yagi  N. Miyajima  T. Sumita 《Physics and Chemistry of Minerals》2002,29(8):532-537

 In order to clarify Al₂O₃ content and phase stability of aluminous CaSiO₃-perovskite, high-pressure and high-temperature transformations of Ca₃Al₂Si₃O₁₂ garnet (grossular) were studied using a MA8-type high-pressure apparatus combined with synchrotron radiation. Recovered samples were examined by analytical transmission electron microscopy. At pressures of 23–25 GPa and temperatures of 1000–1600 K, grossular garnet decomposed into a mixture of aluminum-bearing Ca-perovskite and corundum, although a metastable perovskite with grossular composition was formed when the heating duration was not long enough at 1000 K. On release of pressure, this aluminum-bearing CaSiO₃-perovskite transformed to the “LiNbO₃-type phase” and/or amorphous phase depending on its Al₂O₃ content. The structure of this LiNbO₃-type phase is very similar to that of LiNbO₃ but is not identical. CaSiO₃-perovskite with 8 to 25 mol% Al₂O₃ was quenched to alternating lamellae of amorphous layer and LiNbO₃-type phase. On the other hand, a quenched product from CaSiO₃-perovskite with less than 6 mol% consisted only of amorphous phase. Most of the inconsistencies amongst previous studies could be explained by the formation of perovskite with grossular composition, amorphous phase, and the LiNbO₃-type phase. Received: 11 April 2001 / Accepted: 5 July 2002  相似文献   

High pressure transitions in the system KAlSi3O8-NaAlSi3O8     

Atsushi Yagi  Toshihiro Suzuki  Masaki Akaogi 《Physics and Chemistry of Minerals》1994,21(1-2):12-17

Phase relations in the system KAlSi₃O₈-NaAlSi ₃O₈ have been examined at pressures of 5–23 GPa and temperatures of 700–1200° C. KAlSi₃O₈ sanidine first dissociates into a mixture of wadeite-type K₂Si₄O₉, kyanite and coesite at 6–7 GPa, which further recombines into KAlSi₃O₈ hollandite at 9–10 GPa. In contrast, NaAlSi₃O₈ hollandite is not stable at 800–1200° C near 23 GPa, where the mixture of jadeite plus stishovite directly changes into the assemblage of calcium ferrite-type NaAlSiO₄ plus stishovite. Phase relations in the system KAlSi₃O₈-NaAlSi₃O₈ at 1000° C show that NaAlSi₃O₈ component gradually dissolves into hollandite with increasing pressure. The maximum solubility of NaAlSi₃O₈ in hollandite at 1000° C was about 40 mol% at 22.5 GPa, above which it decreases with pressure. Unit cell volume of the hollandite solid solution decreases with increasing NaAlSi₃O₈ component. The hollandite solid solution in this system may be an important candidate as a host mineral of K and Na in the uppermost lower mantle  相似文献   

High-resolution observations of the Orion bright bar     

Omodaka  Toshihiro  Hayashi  Masahiko  Suzuki  Saeko  Hasegawa  Tetsuo  Miyawaki  Ryosuke 《Astrophysics and Space Science》1986,118(1-2):401-404

High resolution strip maps of CS (J=1–0) and H51 line emission across the Orion bright bar are presented. They reveal the existence of a high density molecular layer (molecular sheet) plane parallel to the ionization front. This molecular sheet is redshifted relative to the ambient molecular cloud by about 2 km s^–1. The rapid decrease of the CS emission at about 50 arc sec from the bar suggests that a shock front exists here and the sheet is a post shock layer.Paper presented at the IAU Third Asian-Pacific Regional Meeting, held in Kyoto, Japan, between 30 September–6 October, 1984.This work was carried out under the common use observation program at the Nobeyama Radio Observatory (NRO). NRO, a branch of the Tokyo Astronomical Observatory, University of Tokyo, Japan, is a cosmic radio observing facility open to outside users.  相似文献   

Distribution and sources of organic matter in surficial sediments on the shelf and slope off Tokachi, western North Pacific, inferred from C and N stable isotopes and C / N ratios     

Toshihiro Usui  Seiya Nagao  Masanobu Yamamoto  Koji Suzuki  Isao Kudo  Shigeru Montani  Atsushi Noda  Masao Minagawa 《Marine Chemistry》2006,98(2-4):241-259

Organic carbon (C) and total nitrogen (N) contents and corresponding isotope ratios were determined in surficial sediment (0–3 cm) at 94 stations ranging from 21 to 1995 m water depth off Tokachi, Hokkaido, Japan, to elucidate the distribution and source of sedimentary organic matter. Suspended particulate organic matter (POM) in the seawater and suspended POM and sediment in the Tokachi River were also examined. δ¹³C, δ¹⁵N and C / N ratios of the samples in the Tokachi River suggest that the spring snowmelt is an important process for the transport of terrestrial organic matter to the coastal waters. δ¹³C values of suspended POM in the surface seawater were higher in May and November than in August, while δ¹⁵N values of the POM were higher in May and August than in November. These changes are attributed to seasonal changes in phytoplankton growth rate and nitrate availability. δ¹³C and δ¹⁵N values in the sediments off Tokachi were lowest near the Tokachi River mouth, and increased offshore to constant values that persisted from 134 to 1995 m water depth. The spatial variation in C / N ratios in the sediment mirrored those of δ¹³C and δ¹⁵N. Comparison of δ¹³C, δ¹⁵N and C / N ratios in the sediments off Tokachi with those in the Tokachi River and seawater indicates that about half of the organic matter in the sediment was of terrestrial origin near the Tokachi River mouth, and the sedimentary organic matter from 134 to 1995 m water depth was of marine origin. The organic C content in the sediment was high near the Tokachi River mouth, and also around 1000 m water depth. The C content was significantly correlated with silt plus clay content, with different regression lines for those stations shallower and deeper than 134 m, owing to several stations of higher C content with the elevated C / N ratio on the inner shelf. These results suggest that transport and deposition of organic-rich fine sediment particles by hydrodynamic processes were major factors controlling C content off Tokachi. In addition, the supply of a fraction of terrestrial organic matter with high C / N probably also affected C content on the inner shelf.  相似文献   

Rising motion of a behind-the-limb flare at 35 GHz     

Tatsuji Kato  Toshihiro Omodaka  Mitsumi Fujishita  Kin-Aki Kawabata  Hideo Ogawa 《Solar physics》1982,78(1):137-140

Interferometer observation of a behind-the-limb flare on 7 September, 1977, at 35 GHz ( = 8.6 mm) shows that the microwave non-thermal radio source of the burst is located in the coronal region at the height higher than 7000 km above the photosphere and rises gradually with the velocity of about 30 km s^-1.  相似文献   

Incorporation of U,Pb and Rare Earth Elements in Calcite through Crystallisation from Amorphous Calcium Carbonate: Simple Preparation of Reference Materials for Microanalysis     

Yusuke Miyajima  Ayaka Saito  Hiroyuki Kagi  Tatsunori Yokoyama  Yoshio Takahashi  Takafumi Hirata 《Geostandards and Geoanalytical Research》2021,45(1):189-205

Uncertainty for elemental and isotopic measurements in calcite by LA‐ICP‐MS is largely controlled by the homogeneity of the reference materials (RMs) used for calibration and validation. In order to produce calcite RMs with homogeneous elemental and isotopic compositions, we incorporated elements including U, Pb and rare earth elements into calcite through heat‐ and pressure‐induced crystallisation from amorphous calcium carbonate that was precipitated from element‐doped reagent solution. X‐ray absorption spectra showed that U was present as U(VI) in the synthesised calcite, probably with a different local structure from that of aqueous uranyl ions. The uptake rate of U by our calcite was higher in comparison with synthetic calcite of previous studies. Variations of element mass fractions in the calcite were better than 12% 2RSD, mostly within 7%. The ²⁰⁷Pb/²⁰⁶Pb ratio in the calcite showed < 1% variations, while the ²³⁸U/²⁰⁶Pb ratio showed 3–24% variations depending on element mass fractions. Using the synthetic calcite as primary RMs, we could date a natural calcite RM, WC‐1, with analytical uncertainty as low as < 3%. The method presented can be useful to produce calcite with controlled and homogeneous element mass fractions and is a promising alternative to natural calcite RMs for U‐Pb geochronology.  相似文献   

Oxygen and carbon isotope records of cultured freshwater pearl mussel <Emphasis Type="Italic">Hyriopsis</Emphasis> sp. shell from Lake Kasumigaura,Japan     

Toshihiro Yoshimura  Rei Nakashima  Atsushi Suzuki  Noriko Tomioka  Hodaka Kawahata 《Journal of Paleolimnology》2010,43(3):437-448

We present oxygen and carbon isotope ratios and the morphological structure of the cultured freshwater pearl mussel (Hyriopsis sp., Unionidae) shell and pearl. The number of first-order fluctuations of δ¹⁸O of the outer shell layer along the maximum growth axis was consistent with the number of cultured years. The dominant factor controlling annual δ¹⁸O fluctuations was water temperature with a minor contribution from the variation in δ¹⁸O of ambient water, especially during the rainy season. The δ¹³C values were approximately constant throughout the life of the mussel, suggesting that the contributions of body size to δ¹³C of the shell were minor. We observed nine distinct disturbance rings on the outer surface of the shell. Five rings coincided with the five winter peaks of the δ¹⁸O profile, indicating winter growth cessation below approximately 10°C, probably because of either inactive growth at low water temperatures or reproduction. Summer disturbance rings were not observed in all years. Moreover, some summer rings showed discontinuity in the inner structure. These findings suggest that summer growth cessation may be caused by occasional events such as heavy rains, as the decrease of dissolved oxygen concentration. The δ¹⁸O profile and shell structures indicated that shell aragonite was precipitated at close to equilibrium conditions with respect to the oxygen isotope composition of the ambient water. Hyriopsis sp. shells can potentially be used for reconstruction of past hydrologic conditions. The δ¹⁸O of a pearl indicated that calcification occurred over a temperature range of at least 13–23°C. The optimal temperature for pearl calcification in this species is lower than that for marine pearl calcification.  相似文献   

Stable nitrogen isotope composition in sedimentary organic matter as a potential proxy of nitrogen sources for primary producers at a fringing coral reef     

Yu Umezawa  Toshihiro Miyajima  Isao Koike 《Journal of Oceanography》2008,64(6):899-909

The stable nitrogen isotope ratio (δ ¹⁵N) in macroalgae is effectively used as a time-integrated bioindicator to record nitrogen sources for primary producers during their growing periods in aquatic ecosystems. However, the utility of this tool is limited because the occurrence of these organisms is often restricted in space and time. To investigate the potential of chemical composition in sedimentary organic matter (SOM) as a proxy for time-integrated environmental conditions, nitrogen (N) and carbon (C) contents and their stable isotope ratios (δ ¹⁵N and δ ¹³C) were determined, and systematically cross-checked against corresponding values in macroalgae at the Shiraho fringing reef in Okinawa, Japan. Preliminary trials showed that δ ¹⁵N in SOM processed by the “wash-out method” for δ ¹³C analysis yielded similar δ ¹⁵N values to the bulk sediment, despite the loss of some SOM during the process. The amounts of organic matter and the ratio of the HCl-insoluble portion were variable within the reef, probably reflecting local vegetation and subsequent decomposition. The distribution of δ ¹⁵N and δ ¹³C in SOM showed similar trends to those of macroalgae, with mostly constant differences of 1.4‰ and −6.7‰, respectively. These differences throughout the reef appeared to be explained in terms of mixed contributions from macrophyte and epibenthic microalgae growing in different seasons and years, with their debris undergoing diagenetic alteration. Therefore, macroalgae and SOM δ-values can be used in a complementary manner, over various time scales, as indicators of the integrated effect of dissolved inorganic nitrogen (DIN) sources on coral reef ecosystems.  相似文献