ACTIVE system for monitoring volcanic activity: A case study of the Izu-Oshima Volcano,Central Japan     

Hisashi Utada  Yuji Takahashi  Yuichi Morita  Takao Koyama  Tsuneomi Kagiyama 《Journal of Volcanology and Geothermal Research》2007

A system is proposed for the monitoring of changes in the underground structure of an active volcano over time by applying a transient electromagnetic method. The monitoring system is named ACTIVE, which stands for Array of Controlled Transient-electromagnetics for Imaging Volcano Edifice. The system consists of a transmitter dipole used to generate a controlled transient electromagnetic (EM) field and an array of receivers used to measure the vertical component of the transient magnetic field at various distances, with automatic operation of both units. In order to verify the performance of the proposed system, numerical and field experiments were carried out by application of the system to the Izu-Oshima volcano, where a remarkable change in the apparent DC resistivity over time had been detected in association with the eruption in 1986.  相似文献   

Water status in winter wheat grown under salt stress     

M Larry Lopez C~  WANG Rong~  MAO Xue-sen~  Takahashi Hidenori~ 《地理学报(英文版)》2001,11(2):202-208

1 IntroductionSalinization is one of the major problems in arid and semi-arid regions in relation to land use and in particular to agricultural production[1]. Excessive salinity leads to toxicity in crops and reduction of the availability of water to crops, by reducing the osmotic potential of the soil solution[2]. Movement of soil water induces solute transport, and solutes are transferred towards the ground surface by the upward soil-water movement caused by evaporation, resulting in an accu…  相似文献   

Preface     

T. Shimamoto  K. Takemura  K. Fujimoto  H. Tanaka  C. A. J. Wibberley 《Island Arc》2001,10(3-4):357-359

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Observation　and　research　on　ULF　and　VLF　seismo－electromagnetic　radiation     

袁家治  钱书清  赵华兴  任克新 《地震学报(英文版)》1996,9(2):351-355

ＯｂｓｅｒｖａｔｉｏｎａｎｄｒｅｓｅａｒｃｈｏｎＵＬＦａｎｄＶＬＦｓｅｉｓｍｏ－ｅｌｅｃｔｒｏｍａｇｎｅｔｉｃｒａｄｉａｔｉｏｎＪＩＡ－ＺＨＩＹＵＡＮ（袁家治）；ＫｏｚｏＴａｋａｈａｓｈｉ；ＳＨＵ－ＱＩＮＧＱＩＡＮ（钱书清），ＹｏｋｉｏＦｕｊｉｎａｗ...  相似文献   

Contamination by organochlorine compounds in walleye pollock (Theragra chalcogramma) from the Bering Sea, Gulf of Alaska and the Japan Sea     

de Brito AP  Ueno D  Takahashi S  Tanabe S 《Marine pollution bulletin》2002,44(2):172-177

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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   

Importance of the mixed-phase cloud distribution in the control climate for assessing the response of clouds to carbon dioxide increase: a multi-model study   总被引：1，自引：1，他引：1  

Yoko Tsushima  S. Emori  T. Ogura  M. Kimoto  M. J. Webb  K. D. Williams  M. A. Ringer  B. J. Soden  B. Li  N. Andronova 《Climate Dynamics》2006,27(2-3):113-126

We have conducted a multi-model intercomparison of cloud-water in five state-of-the-art AGCMs run for control and doubled carbon dioxide climates. The most notable feature of the differences between the control and doubled carbon dioxide climates is in the distribution of cloud-water in the mixed-phase temperature band. The difference is greatest at mid and high latitudes. We found that the amount of cloud ice in the mixed phase layer in the control climate largely determines how much the cloud-water distribution changes for the doubled carbon dioxide climate. Therefore evaluation of the cloud ice distribution by comparison with data is important for future climate sensitivity studies. Cloud ice and cloud liquid both decrease in the layer below the melting layer, but only cloud liquid increases in the mixed-phase layer. Although the decrease in cloud-water below the melting layer occurs at all latitudes, the increase in cloud liquid in the mixed-phase layer is restricted to those latitudes where there is a large amount of cloud ice in the mixed-phase layer. If the cloud ice in the mixed-phase layer is concentrated at high latitudes, doubling of carbon dioxide might shift the center of cloud water distribution poleward which could decrease solar reflection because solar insolation is less at higher latitude. The magnitude of this poleward shift of cloud water appears to be larger for the higher climate sensitivity models, and it is consistent with the associated changes in cloud albedo forcing. For the control climate there is a clear relationship between the differences in cloud-water and relative humidity between the different models, for both magnitude and distribution. On the other hand the ratio of cloud ice to cloud-water follows the threshold temperature which is determined in each model. Improved measurements of relative humidity could be used to constrain the modeled representation of cloud water. At the same time, comparative analysis in global cloud resolving model simulations is necessary for further understanding of the relationships suggested in this paper.  相似文献   

Importance of geochemical transformations in determining submarine groundwater discharge-derived trace metal and nutrient fluxes     

Aaron J. Beck  Yoko Tsukamoto  Antonio Tovar-Sanchez  Miguel Huerta-Diaz  Henry J. Bokuniewicz  Sergio A. Sañudo-Wilhelmy 《Applied Geochemistry》2007

Seasonal (Spring and Summer 2002) concentrations of dissolved (<0.22 μm) trace metals (Ag, Al, Co, Cu, Mn, Ni, Pb), inorganic nutrients (NO₃, PO₄, Si), and DOC were determined in groundwater samples from 5 wells aligned along a 30 m shore-normal transect in West Neck Bay, Long Island, NY. Results show that significant, systematic changes in groundwater trace metal and nutrient composition occur along the flowpath from land to sea. While conservative mixing between West Neck Bay water and the groundwaters explains the behavior of Si and DOC, non-conservative inputs for Co and Ni were observed (concentration increases of 10- and 2-fold, respectively) and removal of PO₄ and NO₃ (decreases to about half) along the transport pathway. Groundwater-associated chemical fluxes from the aquifer to the embayment calculated for constituents not exhibiting conservative behavior can vary by orders of magnitude depending on sampling location and season (e.g. Co, 3.4 × 10²– 8.2 × 10³ μmol d⁻¹). Using measured values from different wells as being representative of the true groundwater endmember chemical composition also results in calculation of very different fluxes (e.g., Cu, 6.3 × 10³ μmol d⁻¹ (inland, freshwater well) vs. 2.1 × 10⁵ μmol d⁻¹(seaward well, S = 17 ppt)). This study suggests that seasonal variability and chemical changes occurring within the subterranean estuary must be taken into account when determining the groundwater flux of dissolved trace metals and nutrients to the coastal ocean.  相似文献   

Poisson's ratios of the upper and lower crust and the sub-Moho mantle beneath central Honshu, Japan     

Motoo Ukawa  Yoshio Fukao 《Tectonophysics》1981,77(3-4)

Poisson's ratios of the upper and lower crust and the sub-Moho mantle beneath central Honshu, Japan, are investigated using three independent methods that are based on S to P ratios of apparent velocities, the Wadati diagrams and an inversion of P and S arrivals. Shallow earthquakes at distances of 200—500 km from the Nagoya University Telemeter Network are used for the apparent velocity ratio method. Crustal and subcrustal earth-quakes under the network are used for the other two methods. The network consists of wide-band seismometers with three components which are particularly suitable for detecting S waves. The three different methods give a consistent result for Poisson's ratio σ, that is, (1) σ = 0.23 ± 0.01 in the upper crust, (2) σ = 0.26−0.28 in both the lower crust and in the sub-Moho mantle. The result indicates a sharp contrast in σ between the upper and the lower crust rather than at the Moho. The low σ in the upper crust can only be explained by the presence of a substantial amount of free quartz, indicating granitic rocks. A higher σ in the lower crust suggests that this portion is presumably less saturated in silica and may be even undersaturated, pointing to intermediate to mafic rocks. The sub-Moho σ is almost equal to the σ averaged over the entire upper mantle that has been estimated from the Wadati diagrams of deep shocks beneath Japan but is higher than those calculated from Pn and Sn velocities in oceanic and stable continental regions.  相似文献   

Partitioning of Ni²⁺, Co²⁺, Fe²⁺, Mn²⁺ and Mg²⁺ between olivine and silicate melts: compositional dependence of partition coefficient   总被引：1，自引：0，他引：1  

Eiichi Takahashi 《Geochimica et cosmochimica acta》1978,42(12):1829-1844

Partitioning of Ni²⁺, Co²⁺, Fe²⁺, Mn²⁺ and Mg²⁺ between olivine and silicate melts has been determined near the join (Mg_0.5·-Fe_0.5)₂SiO₄-K₂O 4SiO₂ and for seven different basaltic compositions. The experiments were made at 1 atm total pressure, 1500-1100°C, and under moderate to reducing oxygen fugacities. The concentration factor, defined as K^MO = (MO)^ol/(MO)^liq (molar ratio), increases markedly for all the cations studied as the olivine component of the liquid decreases. Much of the increase in K^MO is considered as due to the compositional effect of the coexisting liquid: the temperature effect on K^MO is probably opposite to the compositional effect (K^MO decreases as temperature decreases).The partition coefficient K^MO-MgO = (MO/MgO)^ol/(MO/MgO)^liq for the reaction, M_ol²⁺ + Mg_liq²⁺ = M_liq²⁺ + Mg_ol²⁺. is relatively constant over a wide range of SiO₂ content of the liquid, except in the case of Ni²⁺. The partition coefficients have similar ranges both in synthetic and natural rock systems: K^NiO-MgO = 1.8–3.0, K^CoO-MgO = 0.6–0.8, K^FeO-MgO = 0.27–0.38, and K^MnO-MgO = 0.23–0.32. There is a systematic variation in the partition coefficient K^MO-MgO with the composition of liquid; K^MO-MgO increases with increasing SiO₂ content of melt. The partition coefficients for Co²⁺, Fe²⁺ and Mn²⁺ are useful to test the equilibration of olivine with magma of a wide compositional range.  相似文献