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81.
Xiu Luo Hiroshi Haya Tomoaki Inaba Tomoki Shiotani 《Soil Dynamics and Earthquake Engineering》2006,26(12):1101-1110
One difficult task for the seismic diagnosis of existing structures is how to nondestructively evaluate the damage degree of invisible substructures, such as embedded foundations. To diagnose substructures efficiently, a method for nondestructive inspection is developed by applying acoustic emission (AE) technique. As a newly proposed method, characteristics of secondary AE induced by train operations were investigated, and experiments using model piles and in-situ AE monitoring of in-service railway bridges conducted under railroad traffic, from which it was demonstrated that the proposed method is practicable enough to detect invisible defects in structures. A new index, known as RTRI (ratio of Repeated Train load at the onset of AE activity to Relative maximum load for Inspection period) is proposed for structural damage qualification based on the results of in-situ AE monitoring. 相似文献
82.
Masao Ohno Tsutomu Sato Kenji Notsu Hiroshi Wakita Kunio Ozawa 《Pure and Applied Geophysics》2006,163(4):647-655
Anomalous water level changes were observed at two wells associated with seismic swarm activity off Izu Peninsula on March,
1997. These are coseismic water level drops followed by gradual postseismic water level rise at the time of large earthquakes
during the swarm activity. The post-seismic water level rises, which can be fitted by an exponential function with a time
constant of about six hours, are explained in terms of the horizontal pressure diffusion due to the pressure gradient in the
aquifer induced by the coseismic static strain. 相似文献
83.
Fog and rain water chemistry at Mt. Fuji: A case study during the September 2002 campaign 总被引:2,自引:0,他引:2
Koichi Watanabe Yusaku Takebe Nobuhiro Sode Yasuhito Igarashi Hiroshi Takahashi Yukiko Dokiya 《Atmospheric Research》2006,82(3-4):652
Measurements of fog and rain water chemistry at the summit of Mt. Fuji, the highest peak in Japan, as well as at Tarobo, the ESE slope of Mt. Fuji in September 2002. The pH of fog and rain water sampled at Mt. Fuji varied over a range of 4.0–6.8. Acidic fogs (pH < 5.0) were observed at the summit when the air mass came from the industrial regions on the Asian continent. The ratio of [SO42−]/[NO3−] in the fog water was lower at Tarobo than at the summit. High concentrations of Na+ and Cl− were determined in the rain water sampled at the summit, possibly because of the long-range transport of sea-salt particles raised by a typhoon through the middle troposphere. The vertical transport of sea-salt particles would influence the cloud microphysical properties in the middle troposphere. Significant loss of Mg2+ was seen in the rain water at the summit. The concentrations of peroxides in the fog and rain water were relatively large (10–105 μM). The potential capacity for SO2 oxidation seems to be strong from summer to early autumn at Mt. Fuji. The fog water peroxide concentrations displayed diurnal variability. The peroxide concentrations in the nighttime were significantly higher than those in the daytime. 相似文献
84.
Hiroshi Taura Hisayoshi Yurimoto Kei Kurita Shigeho Sueno 《Physics and Chemistry of Minerals》1998,25(7):469-484
Partition coefficients between olivine and melt at upper mantle conditions, 3 to 14 GPa, have been determined for 27 trace
elements (Li, Be, B, Na, Mg, Al, Si, P, K, Ca, Sc, Ti, V, Cr, Mn, Fe, Co, Ni, Cu, Rb, Sr, Y, Zr, Cs, Ba, La and Ce) using
secondary-ion mass-spectrometry (SIMS) and electron-probe microanalysis (EPMA). The general pattern of olivine/melt partitioning
on Onuma diagrams resembles those reported previously for natural systems. This agreement strongly supports the argument that
partitioning is under structural control of olivine even at high pressure. The partition coefficients for mono- and tri-valent
cations show significant pressure dependence, both becoming larger with pressure, and are strongly correlated with coupled
substitution into cation sites in the olivine structure. The dominant type of trace element substitution for mono- and tri-valent
cations into olivine changes gradually from (Si, Mg)↔(Al, Cr) at low pressure to (Si, Mg)↔(Al, Al) and (Mg, Mg)↔(Na, Al) at
high pressure. The change in substitution type results in an increase in partition coefficients of Al and Na with pressure.
An inverse correlation between the partition coefficients for divalent cations and pressure has been observed, especially
for Ni, Co and Fe. The order of decreasing rate of partition coefficient with pressure correlates to strength of crystal field
effect of the cation. The pressure dependence of olivine/melt partitioning can be attributed to the compression of cation
polyhedra induced by pressure and the compensation of electrostatic valence by cation substitution.
Received: March 6, 1997 / Revised, accepted: March 12, 1998 相似文献
85.
S. Uyeda 《International Journal of Earth Sciences》1981,70(2):552-569
In the framework of plate tectonics, the basic mechanism operating in the trencharc-back arc systems is believed to be the subduction of oceanic lithosphere. This model, however, was developed more or less as a logical consequence of sea-floor spreading. The question then is whether or not the subduction model can explain all the major features of the trench-arc-back arc systems. Many features, such as thrust type inter-plate earthquakes and deep earthquakes along Wadati-Benioff zones, are readily explained. But, the occurrences of extentional spreading and high heat flow in the back arc region and arc volcanism are difficult to explain. An approach to solve these problems may be found in what may be called “comparative subductology”: there seem to exist two basically different modes of subduction; one — Chilean type — causing compressional stress regime in the arc and back arc regions, the other — Mariana type — causing tensional. World's subduction zones are classified in terms of the postulated two modes, and some tectonic implications and causes of the two modes are discussed. 相似文献
86.
87.
88.
The Resonance Capacity Method is proposed for the earthquake response analysis of hysteretic structures. Resonance Capacity is a physical quantity of structures which is related to the hysteretic energy absorbed by structures in one cycle and is equated to the acceleration, velocity and displacement amplitudes α0, d0 and d0 of earthquake ground motions at resonance.1 According to the idealized trapezoidal approximation of earthquake ground motions in the logarithmic period–velocity plane as proposed by Veletsos and Newmark,8 the Resonance Capacity property applies in each period range, short, medium and long, where α0, v0 and d0 respectively are approximately constant. In the medium range of periods, the energy dissipated in hysteretic loops and the deformation amplitudes of a single-degree system with elasto–plastic force–deformation relationships are calculated for the case of El Centro 1940, 18 May earthquake, by this Resonance Capacity Method. The result is compared with results from conventional numerical response analyses obtained by Berg and Thomaides,14 Kato and Akiyama12 and Veletsos and Newmark,8 and the general agreement is seen to be good. Therefore, it may be possible to apply this Resonance Capacity Method over the entire range of periods. By means of this method the earthquake response analysis of hysteretic systems can be performed easily, and the hysteretic energy and fatigue characteristics of structures may be taken into account directly, up to the point of fracture. 相似文献
89.
Norimichi Takenaka Tohru Daimon Akihiro Ueda Keiichi Sato Masaru Kitano Hiroshi Bandow Yasuaki Maeda 《Journal of Atmospheric Chemistry》1998,29(2):135-150
Nitrite oxidation in the tropospheric aqueous phase by freezing was evaluated by freezing a field sample. Nitrite oxidation by dissolved oxygen in the freezing process is much faster than by other oxidation processes, such as reactions with ozone, hydrogen peroxide or dissolved oxygen in an aqueous solution at pHs 3 to –6. At pH 4.5 and 25°C, the lifetime of nitrite in the aqueous phase is ca. 1 hr in oxidation by ozone (6×10-10 mol dm-3), ca. 10 hr in oxidation by H2O2 (2×10-4 mol dm-3), and 7.5 hr (Fischer and Warneck, 1996) in photodissociation at midday in summer. Under the same conditions at a temperature below 0°C, the lifetime of nitrite in the freezing process is estimated as ca. 2 sec when the droplets are frozen within a second. The reaction by freezing is affected by the presence of salts, such as NaCl or KCl, or orgnaic compounds, such as methanol or acetone. The results of freezing a field rain or fog sample showed that nitrite oxidation proceeds below pH 6, and the conversion ratio of nitrate from nitrite increases with decreasing pH. The oxidation of nitrite by freezing was also observed in freezing fog particles generated by an ultrasonic humidifier. The ratios of the concentrations of ions in the winter sample to those in the summer sample (or those in the fog sample) were almost the same values. However, the concentration of nitrite in the winter sample was lower than that estimated by the ratios of other ions. From the present study, it seems that the freezing process plays an important role in the nitrite sink process in the tropospheric aqueous phase. 相似文献
90.
It has been found that samples consisting of a homogeneous vitrinite show a good ESR correlation of spin concentration with geothermal parameters and that a graph of ESR line width vs g-value can be useful in the identification of the maceral and the determination of the coalification rank. 相似文献