Indigenous Knowledge on Soil Classification of Ethnic Groups in Luang Prabang Province of the Lao PDR     

Linkham Douangsavan Vongpaphane Manivong Anan Polthanee Roengsak Katawatin Yoshio Inoue 《山地科学学报》2006,3(3):247-258

Introduction Traditional agriculture based on indigenous knowledge (IK) has been practiced in many areas for centuries. Such practices are often the basis of very sustainable technologies, which are potentially suitable for developmental programs. Polthanee (2001) reported that such farmer practices have been repeatedly found to be valid, rational and usually suited to the local environmental conditions. Moreover, with increased under- standing of agro-ecosystems, professionals in agricultura…  相似文献   

Open boundary value problems in ocean dynamics by finite elements     

Toyoki Tanaka  Yoshio Ono  Toshikazu Ishise 《Advances in water resources》1982,5(1):21-28

This paper presents recent results of application of the finite element models to wave overtopping and wave run-up problems in ocean dynamics. Open boundaries are prescribed as natural boundary condition obtained from the continuity equation of the Galerkin finite element formulation. The numerical results are, in general, reasonably good agreements with the histrical field data.  相似文献   

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

Keisuke Fukushi  Tomonori Sugiura  Tomoaki Morishita  Yoshio Takahashi  Noriko Hasebe  Hiroshi Ito 《Applied Geochemistry》2010

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.  相似文献   

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

Yoshio Takahashi  Mika Yamamoto  Kazuya Tanaka 《Geochimica et cosmochimica acta》2010,74(19):5443-5796

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.  相似文献   

Occurrence of arsenic (V) in forearc mantle serpentinites based on X-ray absorption spectroscopy study     

Keiko Hattori  Yoshio Takahashi  Bo Johanson 《Geochimica et cosmochimica acta》2005,69(23):5585-5596

We examined As concentration, mineralogical site, and oxidation state in the serpentinites associated with the Tso Morari eclogitic rocks in the Indus suture zone, northwest Himalaya, to examine how highly fluid-soluble elements like As are transferred from slabs to arc magmas in subduction zones. The serpentinite samples represent hydrated peridotites at the base of the mantle wedge beneath Eurasia, and were exhumed from a depth of ∼100 km during subduction of the Indian continental margin. The bulk serpentinite samples contain total As concentrations ranging from 6 to 275 ppm. Arsenic in the samples is most likely present with magnetite and antigorite, since electron probe analysis yielded up to 90 ppm As in these minerals. X-ray absorption near-edge structure spectra indicate that As in serpentinites is mostly As(V) and that the neighboring atoms of As are O, although there are minute grains of sulfides and arsenides. The ratio of As(V) to total As is greater in samples with higher As contents, suggesting that the major source of As was oxidized As(V), introduced to the mantle wedge. Arsenic(V), originally adsorbed on Fe-oxides in slabs and overlying sediments, was most likely liberated during their subduction and incorporated subsequently in the overlying mantle wedge. Our data constrain the introduction of As into the mantle wedge at relatively shallow levels, much shallower than 25 km. Arsenic incorporated in the serpentinites was transported to deeper levels by mantle flow downward along the subduction zone, to be subsequently exhumed together with eclogitic rocks.  相似文献   

Scattering attenuation, dispersion and reflection of SH waves in two-dimensional elastic media with densely distributed cracks     

Yoshio Murai 《Geophysical Journal International》2007,168(1):211-223

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An atomic level study of rhenium and radiogenic osmium in molybdenite   总被引：1，自引：0，他引：1  

Yoshio Takahashi  Tomoya Uruga  Hajime Tanida  Keiko H. Hattori 《Geochimica et cosmochimica acta》2007,71(21):5180-5190

Local atomic structures of Re and radiogenic Os in molybdenite from the Onganja mine, Namibia, were examined using X-ray absorption fine structure (XAFS). Rhenium L_III-edge X-ray absorption near-edge structure (XANES) and extended X-ray absorption fine structure (EXAFS) show that the oxidation state of Re, the interatomic distances between Re and the neighboring atoms, and the coordination number of Re to S are very similar to those of Mo in molybdenite. The results confirm that Re is present as Re(IV) in the Mo site in molybdenite.Measurement of L_III-edge XANES and EXAFS of a minor concentration (8.55 ppm) of radiogenic Os was accomplished in fluorescence mode by removing the interfering X-rays from Re and other elements using a crystal analyzer system. The data indicate that the oxidation state of radiogenic Os is Os(III) and Os(IV) and clearly different from Os(II) in natural sulfide minerals, such as OsS₂ (erlichmanite). XANES data also suggest that radiogenic Os does not form a secondary Os phase, such as OsS₂ or Os metal, in molybdenite.EXAFS of radiogenic Os was successfully simulated assuming that Os is present in the Mo site in molybdenite. The data are consistent with the XANES data; Os does not form Os phases in molybdenite. The EXAFS simulation showed that the interatomic distance between Os and S is 2.27 Å, which is 0.12 Å smaller than the distances of Re-S and Mo-S (2.39 Å) in molybdenite. Similar valences and ionic sizes of Re and Mo in molybdenite support the fact that large amounts of Re can be incorporated into the Mo site as has been observed in previous studies, whereas the different properties of Os compared to Mo and Re suggested here support much lower abundance of common Os in molybdenite. This makes molybdenite an ideal mineral for the Re-Os geochronometer as shown in many studies. However, the shorter distance between radiogenic Os and S compared to those of Re-S and Mo-S in molybdenite suggests that the radiogenic Os has a smaller ionic size than Re(IV) and Mo(IV). Furthermore, Os may be partly present as Os(III). Smaller and lower charge Os can diffuse faster than larger and higher charge Re in molybdenite at a given set of conditions. Hence, our study provides an atomic-level explanation for the high mobility of Os compared to Re, which has been suggested by earlier workers using laser ablation ICP-MS.  相似文献   

Research Note the Matrix Element For A Transversely Isotropic Earth Model     

Naoki Shibata  Naoki Suda  Yoshio Fukao 《Geophysical Journal International》1990,100(2):315-318

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Foreword     

Y. Katsui  S. Aramaki  S. Matsuo  O. Oshima  T. Tiba  Y. Sawada 《Bulletin of Volcanology》1990,52(Z1):i-vi

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Seismic return motion     

Masayuki Kikuchi  Yoshio Fukao 《Physics of the Earth and Planetary Interiors》1976,12(4):343-349

Possibilities of backswing of fault displacement are investigated on the basis of a simple crack model. Although it has been suggested that the backswing would not occur in real earthquakes because of friction, there is evidence that some earthquakes might have caused return motion “locally” on the fault surface. This paper attempts to derive conditions for such local return motion. Spatial extension of the crack beyond the stress-filled region into the stress-deficient region gives a favorable site for the return motion, the site being just outside the stress-filled region. In our model the return motion occurs at this site when the frictional stress is less than about 30% of the regional stress in the stress-filled region. The overall return motion, on the other hand, would not occur unless the frictional stress is less than 10% of the regional stress.  相似文献