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171.
172.
Based on the geological tectonics, aftershock activity, earthquake surface rupture and peak ground motion, the geometric and dynamic characteristics of seismogenic tectonics about the 1995 Hanshin earthquake are analysed. Nojima fault and Rokko fault have the same trending direction, but opposite dips. Their rising and falling plates are in symmetrically diagonal distribution. The two faults can be defined as thrust-strike slip faults and constitute a pivotal strike-slip fault. The earthquake just occurred at the pivot, which is the seismotectonics for the earthquake to develop and occur. The pivotal movement along a strike-slip fault often leads to the occurrence of large earthquakes, whose dynamic process can be demonstrated by the stress analysis on the torsion of a beam with rectangle section. The displacement of earthquake surface rupture, aftershock density and peak acceleration change in a certain range of epicentral distance just similar as the shear stress changes from the center to the sides in the rectangle section. The distribution characteristics of the heaviest damage areas are also discussed in the article from the aspects of special geological tectonics and seismotectonic condition. The result obtained from the article can be applied not only to realizing the potencial earthquake sources in middle-long time, but also to build reasonably the prediction model about earthquake hazard. 相似文献
173.
Mina Yutani Takehiko Yagi Hitoshi Yusa Tetsuo Irifune 《Physics and Chemistry of Minerals》1997,24(5):340-344
In situ X-ray diffraction experiments of calcium ferrite-type MgAl2O4 have been carried out using a diamond anvil cell combined with synchrotron radiation and an imaging plate X-ray detector
under hydrostatic pressures up to 9 GPa. The observed unit-cell volumes at various pressures were fitted to the Birch-Murnaghan
equation of state, yielding a bulk modulus of K
T
0= 241(3) GPa when K′
T
0=4 is assumed. This relatively large bulk modulus of calcium ferrite-type MgAl2O4 is consistent with that expected from the systematic relation between bulk modulus and molar volume for the most compounds
possessing fcc oxygen packing.
Received March 5, 1996/Revised, accepted October 15, 1996 相似文献
174.
175.
Michio J. Kishi Hitoshi Motono Makoto Kashiwai Atsushi Tsuda 《Journal of Oceanography》2001,57(5):499-507
A vertical one-dimensional ecosystem model with vertical migration of zooplankton was constructed and applied to Station A-7
off Sanriku district of Japan in the northwest Pacific Ocean. The model consists of an eight-compartment ecosystem model coupled
with a physical model of the oceanic mixed layer. The transition of phytoplankton species responsible for the spring bloom
is well reproduced by this model with vertical migration of zooplankton but is not simulated by the model without vertical
migration. This new model also simulates an observed inter-annual variability of the spring bloom, with the timing and intensity
of the simulated bloom in a given year depending upon the strength of mixing during the preceding winter.
This revised version was published online in August 2006 with corrections to the Cover Date. 相似文献
176.
The authors report here halogen concentrations in pore waters and sediments collected from the Mallik 5L-38 gas hydrate production research well, a permafrost location in the Mackenzie Delta, Northwest Territories, Canada. Iodine and Br are commonly enriched in waters associated with CH4, reflecting the close association between these halogens and source organic materials. Pore waters collected from the Mallik well show I enrichment, by one order of magnitude above that of seawater, particularly in sandy layers below the gas hydrate stability zone (GHSZ). Although Cl and Br concentrations increase with depth similar to the I profile, they remain below seawater values. The increase in I concentrations observed below the GHSZ suggests that I-rich fluids responsible for the accumulation of CH4 in gas hydrates are preferentially transported through the sandy permeable layers below the GHSZ. The Br and I concentrations and I/Br ratios in Mallik are considerably lower than those in marine gas hydrate locations, demonstrating a terrestrial nature for the organic materials responsible for the CH4 at the Mallik site. Halogen systematics in Mallik suggest that they are the result of mixing between seawater, freshwater and an I-rich source fluid. The comparison between I/Br ratios in pore waters and sediments speaks against the origin of the source fluids within the host formations of gas hydrates, a finding compatible with the results from a limited set of 129I/I ratios determined in pore waters, which gives a minimum age of 29 Ma for the source material, i.e. at the lower end of the age range of the host formations. The likely scenario for the gas hydrate formation in Mallik is the derivation of CH4 together with I from the terrestrial source materials in formations other than the host layers through sandy permeable layers into the present gas hydrate zones. 相似文献
177.
Taiji Chida Yuichi Niibori Osamu Tochiyama Hitoshi Mimura Koichi Tanaka 《Applied Geochemistry》2007,22(12):2810-2816
Cementitious materials used for radioactive waste repository construction complicate the performance assessment of radioactive waste systems because the use of cement may greatly alter the pH (8–13) of groundwater and release constituents such as calcium ions. Under such conditions, it is important to clarify also the dynamic behavior of silica (silicic acid), in order to evaluate the alteration in the chemical and physical properties of the fractured layer or the host rock surrounding the repository. Since silica undergoes polymerization, precipitation or dissolution depending on the pH and/or temperature, the behavior of silica would be greatly complicated in the presence of other ions. This study is focused on the deposition rates of polysilicic acid and soluble silicic acid with up to 10−3 M Ca ions. In the experiment, Na2SiO3 solution (250 mL, pH > 10, 298 K) was poured into a polyethylene vessel containing amorphous silica powder (0.5 g), and a buffer solution, HNO3, and CaNO3 as Ca ions were sequentially added into the vessel. The pH of the solution was set to 8. The silica, initially in a soluble form at pH > 10 (1.4 × 10−2 M), became supersaturated and either deposited on the solid surface or changed into the polymeric form. Then the concentrations of both poly- and soluble silicic acid were monitored over a 40-day period. The decrease of polysilicic acid became slow with an increase in the concentration of Ca ions in the range of up to 10−3 M. In general, the addition of electrolytes to a supersaturated solution accelerates the aggregation and precipitation of polymeric species. However, the experimental result showed that polysilicic acid in the presence of Ca ions is apparently stable in solution, compared with that under a Ca-free condition. On the other hand, the concentration of soluble silicic acid in the presence of Ca ions immediately became metastable, that is, slightly higher than the solubility of soluble silicic acid. Its dynamic behavior was similar to that in the Ca-free condition. 相似文献
178.
Geochemical Process of Gas Hydrate Formation in the Nankai Trough Based on Chloride and Isotopic Anomalies in Interstitial Water 总被引:2,自引:0,他引:2
Abstract: Interstitial water expelled from gas hydrate-bearing and -free sediments in the Nankai Trough are analyzed in terms of Cl-, SO4 2 -, δ18 O and δD. The baselines for the Cl- concentration and δ18 O value are close to seawater values (530 mM and 0%), indicating that the interstitial water is of seawater origin. The δD values decrease with depth, implying isotopic exchange of hydrogen between upwelling biogenic methane depleted in D and interstitial water. The Cl- concentrations in gas hydrate-bearing sediments are anomalously low, while the δ18 O and δD values are both high, suggesting that the water forming these gas hydrates was poor in Cl- and enriched in 18 O and D during gas hydrate formation. Calculation of the gas hydrate saturations using Cl "and δ18 O anomalies gives results of up to 80 % in sand, and shows that the δ18 O baseline is not consistent with the Cl" baseline. The δ18 O baseline increases by +1% in gas hydrate-free clay and silt. This is considered to be caused by clustering of water molecules after gas hydrate dissociation in response to the upward migration of the base of gas hydrate stability, as indicated by the presence of a double bottom-simulating reflector at this site. The water clusters enriched in 18 O are responsible for the increase in the δ18 O baseline with normal Cl". The abrupt shallowing of the base of gas hydrate stability may induce the dissociation of gas hydrates and the accumulation of gases in the new stability zone, representing a geological process that increases gas hydrate saturation. 相似文献
179.
Munetake Sasaki Koichiro Fujimoto Hitoshi Tsukamoto Takayuki Sawaki Masakatsu Sasada Masanori Kurosawa Masahiko Yagi Yoichi Muramatsu Osamu Kato + Ryo Komatsu + Kaichiro Kasai + Nobuo Doi+ 《Resource Geology》2003,53(2):127-142
Abstract. Cathodoluminescence (CL) color, rare earth element (REE) content, sulfur and oxygen isotopes and fluid inclusions of anhydrite, which frequently filled in hydrothermal veins in the Kakkonda geothermal system, were investigated to elucidate the spatial, temporal and genetical evolution of fluids in the deep reservoir. The anhydrite samples studied are classified into four types based on CL colors and REE contents: type-N (no color), type-G (green color), type-T (tan color) and type-S (tan color with a high REE content). In the shallow reservoir, only type-N anhydrite is observed. In the deep reservoir, type-G anhydrite occurs in vertical veins whereas type-T and -N in lateral veins. Type-S anhydrite occurs in the heat-source Kakkonda Granite. The CL textures revealed that type-G anhydrite deposited earlier than type-T in the deep reservoir, implying that fracture system was changed from predominantly vertical to lateral.
Studies of fluid inclusions and δ34 S and δ18 O values of the samples indicate that type-N anhydrite deposited from diluted fluids derived from meteoric water, whereas type-G, -T and -S anhydrites deposited from magmatic brines derived from the Kakkonda Granite with the exception of some of type-G with recrystallization texture and no primary fluid inclusion, which deposited from fossil seawater preserved in the sedimentary rocks. Type-G, -T and -S anhydrites exhibit remarkably different chondrite-normalized REE patterns with a positive Eu anomaly, with a convex shape (peak at Sm or Eu) and with a negative Eu anomaly, respectively. The difference in the patterns might result from the different extent of hydrothermal alteration of the reservoir rocks and contribution of the magmatic fluids. 相似文献
Studies of fluid inclusions and δ
180.