Simulation analysis of ground liquefaction induced by earthquake

A dynamic effective stress analysis with the finite element method has long been recommended to predict the liquefaction phenomena of sandy soil by authors and Zienkiewicz et al. as well as the similar approaches by the others. Our approach of the analysis is summarized in the first.

Until recently, however, these approaches has not commonly been used as the means of design, although its capability of prediction is appreciated by geotechnicians. This method has been neglected because of the lack of verification studies of soil models of sand and mathematical formulation for boundary problems of liquefaction phenomena. Therefore the verification of the numerical method to evaluate liquefaction potential are urgent requirement of the recent engineering practice. To respond this requirement, extensive numerical studies on the liquefation simulations are performed by DIANA program for shaking table tests which have been conducted by the authors. The test models are soil-structure type models with combination of homogenous ground and partially improved ground by compaction.

The good performance of our approach is proved by the results of numerical simulation showing good agreement with experimental data in terms of response acceleration, excess pore pressure, and deformation profile. It is also demonstrated that the numerical results can provide substantial information to understand the mechanisms of soil ground behavior which is not easily obtained by experiments.

The procedure to identify soil constants for the reflecting surface model is also reported in details.     

Reconstruction of a climate record for the past 140 kyr based on diatom valve flux data from Lake Biwa, Japan

To reconstruct the pattern of past climate change in central Japan during the last 140 kyr, total planktonic diatom valve concentrations (valves g^–1) and fluxes (valves cm^–2 year^–1) of total planktonic diatoms flux (PVF) and individual species were examined using a 140-m core taken from Lake Biwa, Shiga Prefecture. Most records had a sample resolution between approximately 150 and 300 yr. Based on characteristics of past and modern diatom responses to possible climate variables, we interpreted changes in Stephanodiscus suzukii flux (SVF) to reflect changes in phosphorus levels, which reflect, in turn, summer precipitation levels; changes in Aulacoseiva nipponica flux (AVF) reflect winter vertical lake-water mixing induced by winter temperatures and snowfall levels. Thus, changes in total planktonic diatom flux reflect a combination of summer precipitation, winter temperature, and snowfall values. During the 140–101 ka interval, changes in S. suzukii productivity at a millennial timescale may correspond to changes in summer rainfall in central Japan. The disappearance of A. nipponica during the same period could indicate weaker vertical mixing, possibly caused by increased temperatures and decreased snowfall levels in winter. During the 101–70 ka interval, the AVF record shows levels near or above those observed in present times, indicating that winter water temperatures fell within the optimal range for A. nipponica to prosper. Generally low AVF values during the 70–7 ka interval indicate weak winter vertical mixing and cold winters. The many intervals with low PVF values during the same period suggest decreased summer precipitation levels. Between 7 and 0 ka, PVF, SVF, and AVF records show levels near or above those of the present, suggesting winter temperatures favorable for A. nipponica growth, and snowfall and summer precipitation levels probably similar to or above those currently recorded.     

Energy balance of the tidal current in the Obatake Seto Strait

Current measurements made with a Doppler Current Profiler were taken along cross sections in the Obatake Seto Strait, a small strait in the western part of the Seto Inland Sea.The energy loss between two cross sections of the strait was estimated using the control volume analysis of the stationary one-dimensional energy equation. The large energy loss observed in the strait cannot be explained in terms of general bottom friction in the coastal region. The loss is attributed to the form loss, which is accompanied by internal turbulence and vortices generated by the specific topography of the strait, in addition to the loss by friction. This is supported by the fact that the energy loss in the strait differs, depending upon the current direction.     

Uptake of selenium and other oxyanionic elements in marine ferromanganese concretions of different origins

The concentration of selenium in marine ferromanganese concretions varies between 0.02 and 1.2 mg kg⁻¹, with an average of 0.6 mg kg⁻¹. This is about two orders of magnitude lower than previously reported. In contrast to minor cationic elements, the concentrations of selenium are relatively uniform between ferromanganese concretions of different origins, except for hydrothermal crusts. It shows the same trends of element enrichment as other oxyanionic elements. The incorporation of selenium into ferromanganese concretions is attributed to adsorption of selenate on iron and manganese oxides.     

Soil column experiments for iodate and iodide using K-edge XANES and HPLC–ICP-MS

Radioactive iodine is one of the most problematic radionuclides because of its long half life and high mobility. Mobility of iodine depends on the chemical form to a great extent. This paper reports the results of soil column experiments we conducted to evaluate the mobilities of IO₃⁻ and I⁻. In order to determine the mechanisms of adsorption of IO₃⁻ and I⁻ on soil, adsorption isotherms were obtained by batch experiments. Both adsorption isotherms of IO₃⁻ and I⁻ are well explained by Langmuir model. The adsorption maximum of IO₃⁻ is about five times larger than that of I⁻. In the column experiments, iodine distributions between soil and pore water in the soil column were determined at various depths. Chemical forms of iodine in soil and pore water were determined by X-ray absorption near-edge structure (XANES), and high performance liquid chromatography connected to inductively coupled plasma mass spectrometry (HPLC–ICP-MS), respectively. Vertical profiles of iodine in pore water were simulated using Visual MODFLOW. Our results showed, upon I⁻ infiltration through the column, that a small amount of I⁻ adsorbed on soil, and its mobility is mainly controlled by advection and dispersion. The profile of iodine concentration in pore water was well simulated by assuming equilibrium-controlled Langmuir type adsorption without considering any chemical transformations. For the IO₃⁻ addition system into the column, however, IO₃⁻ adsorbed to soil to a larger degree, which causes a much larger retardation effect than I⁻. In addition, reduction of IO₃⁻ to I⁻ was also confirmed in both soil and pore water by XANES and HPLC–ICP-MS, respectively. The fraction of I⁻ increased toward the deeper end in both phases because of its lower affinity for soil than IO₃⁻, where the reduced I⁻ was released to the pore water and transported by the water flow. In this study, such reduction effect was clearly demonstrated by the speciation analyses of iodine in both soil and water phases, which confirmed that the mobility of I⁻ is a dominant factor that controls the fate of iodine in the surface environment.     

Reconstruction of millennial-scale variations in the East Asian summer monsoon over the past 300 ka based on the total carbon content of sediment from Lake Biwa,Japan

The total carbon content analysis for Takashima-oki core extracted from Lake Biwa with time resolutions of approximately 150 years was used to reconstruct millennial-scale climate change in the East Asian monsoon region over the past 300 ka. The total carbon content of the Takashima-oki core is an indirect proxy for the East Asian summer monsoon, because the total carbon content reflects primary productivity within the lake, which is controlled by precipitation in the catchment area. Using these data, we clarify temporal variations in the East Asian summer monsoon prior to MIS 5, which were previously unresolved. The observed variations show a ∼1,500-year cycle that is also recorded by paleoclimate indices in the North Atlantic region. We propose that the East Asian summer monsoon underwent abrupt millennium-scale changes during interglacial stages such as MIS 5 and 7.     

P–V–T equation of state of Ca3Al2Si3O12 grossular garnet

The thermoelastic parameters of synthetic Ca₃Al₂Si₃O₁₂ grossular garnet were examined in situ at high-pressure and high-temperature by energy dispersive X-ray diffraction, using a Kawai-type multi-anvil press apparatus coupled with synchrotron radiation. Measurements have been conducted at pressures up to 20 GPa and temperatures up to 1,650 K: this P, T range covered the entire high-P, T stability field of grossular garnet. The analysis of room temperature data yielded V _0,300 = 1,664 ± 2 ?³ and K ₀ = 166 ± 3 GPa for K^￠₀ K^{\prime}_{0} fixed to 4.0. Fitting of our P–V–T data by means of the high-temperature third order Birch–Murnaghan or the Mie–Grüneisen–Debye thermal equations of state, gives the thermoelastic parameters: (∂K _0,T /∂T) _P  = −0.019 ± 0.001 GPa K⁻¹ and α _0,T  = 2.62 ± 0.23 × 10⁻⁵ K⁻¹, or γ ₀ = 1.21 for fixed values q ₀ = 1.0 and θ ₀ = 823 (Isaak et al. Phys Chem Min19:106–120, 1992). From the comparison of fits from two different approaches, we propose to constrain the bulk modulus of grossular garnet and its pressure derivative to K _T0 = 166 GPa and K^￠_T0 K^{\prime}_{T0}  = 4.03–4.35. Present results are compared with previously determined thermoelastic properties of grossular-rich garnets.     

Iron–bentonite interactions in the Kawasaki bentonite deposit,Zao area,Japan

Greenish veins occurring in brecciated bentonite were found in the Kawasaki bentonite deposit of the Zao region in Miyagi Prefecture, Japan. Their occurrence possibly indicates the interaction of bentonite with Fe-rich hydrothermal solutions. In order to prove the hypothesis and understand the long-term mineralogical and petrographic evolution of bentonite during such interactions, the greenish veins and the surrounding altered bentonite were analyzed using X-ray fluorescence (XRF), scanning electron microscopy (SEM), X-ray diffraction (XRD), electron probe micro-analysis (EPMA), scanning transmission electron microscopy with energy dispersed spectroscopy (STEM-EDS) and micro X-ray absorption near-edge structure (XANES). The greenish veins resulting from hydrothermal solution are composed of mixed-layer minerals consisting of smectite and glauconite (glaucony), pyrite and opal. The occurrences indicate that glaucony and pyrite formed almost simultaneously from hydrothermal solution prior to opal precipitation. The mineral assemblages of the greenish veins and their surroundings indicate that the hydrothermal activity had most likely taken place at a temperature of less than 100 °C and that the pH and Eh conditions of the reacted solution were neutral to alkaline pH and reducing. The unaltered bentonite is composed mainly of Al smectite and opal. These minerals coexist as a mixture within the resolution level of the microprobe analyses. On the other hand, the bentonite in contact with the greenish veins consists of discrete opal grains and dioctahedral Al smectite containing Fe and was altered mineralogically and petrographically by the hydrothermal activity. Both the clay minerals and the opal were formed by dissolution and subsequent precipitation from the interaction of the original bentonite with the hydrothermal solution.     

Incessant excitation of the Earth's free oscillations: global comparison of superconducting gravimeter records

Records of superconducting gravimeters (SGs) at Canberra (Australia), Esashi (Japan), Metsähovi (Finland) and Syowa Stations (Antarctica) were analyzed to search for further evidence of background free oscillations of the Earth. Spectrograms for 1-year period and averaged power spectra for seismically quiet periods were obtained for each of the stations. Anomalous features of the oscillations observed at Syowa Station, such as an apparent seasonal variation and a high intensity at frequencies between 3 and 4 mHz, were absent at the other SG stations. Among the SG stations used in this study, the background free oscillations were detected most consistently and distinctly at Canberra, where the noise level was comparable to that at the IDA quietest station, while that at Syowa Station was close to the critical limit for detecting the oscillations. The background free oscillations provide a good reference to evaluate the noise level in the milliHertz band.     

EXAFS study on the cause of enrichment of heavy REEs on bacterial cell surfaces

Rare earth element (REE) pattern is a unique geochemical tracer and has been measured for various natural materials. Among these, the REE distribution pattern between bacteria and water exhibits anomalous enrichment in the heavy REE (HREE) part, which can act as a signature of bacteria-related materials in natural samples. In this study, the REE binding site on the cell surface of a Gram-positive bacterium (Bacillus subtilis) responsible for HREE enrichment has been identified using extended X-ray absorption fine structure (EXAFS) coupled with a study of the variation in REE distribution patterns. The EXAFS data showed that the HREEs form complexes with multiple phosphate site (including phosphoester site) with a larger coordination number (CN) at lower REE-bacteria ratios ([REE]/[bac]), while light and middle REEs form complexes to the phosphate site with a lower CN. The fraction coordinated to carboxylate increased for all REEs with increasing [REE]/[bac] ratio. On the other hand, the enrichment of HREE in the REE distribution patterns of the bacteria was less marked with increasing [REE]/[bac] ratio. This result is consistent with the EXAFS data, because the REE pattern of surface complex with multiple phosphate in a reference material exhibits a monotonous increase for heavier REE, while phosphate surface complex with a low CN and a carboxylate site reach a maximum around Sm and Eu. Based on these results, it is clear that the REE are primarily bound to the phosphate site and subsequently to the carboxylate site on the bacterial cell surface.Regarding the pH dependence in the range (3 < pH < 7), both the EXAFS and REE pattern data indicate that the fraction of REE-carboxylate increased as the pH increases. The results above obtained for B. subtilis were also valid for Escherichia coli, a Gram-negative bacterium, showing that similar phosphate and carboxylate sites are also available in the cell walls of E. coli, or other Gram negative bacteria. In all our results, the variation in REE patterns correlated with the binding site indicated by EXAFS, showing that the REE pattern itself reflects the binding site of the REE at the bacterial surface for various parameters (pH and [REE]/[bac] ratio). Thus, the REE patterns can be used to estimate the binding sites for lower [REE]/[bac] ratios where spectroscopic techniques cannot be applied.The average bond length between the REE and oxygen was compared for various REE sorbed on bacteria, showing that the bond length for HREE (Er to Lu) was much shorter than those extrapolated from the trend between La and Dy, because of the selective binding of the HREE as the multiple phosphate surface complexes. Our results are consistent with the selective enrichment of the HREE at the bacterial cell surfaces, considering that chemical species with a shorter bond length are more stable. Thus, it is clear that the HREE enrichment at the bacterial cell surfaces is caused by the formation of the multiple phosphate surface complexes. Based on these results, it is suggested that materials having such phosphate sites such as bacteria and bacteria-related materials can induce anomalous HREE enrichment in natural systems.