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1.
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   
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The resistivity structure of Unzen Volcano has been revealed by extensive magnetotelluric surveys since the first eruption on November 17, 1990. This structure comprises a highly resistive surface layer, a low-resistive second layer at several hundred meters depth, interpreted as a water-saturated layer, a resistive third layer, and a low-resistive fourth layer at 10 km depth, possibly related to the deep magmatic activity. The structure has influenced the volcanic activity of Unzen. This activity was characterized by a series of dramatic changes in eruption type: a minor phreatic eruption on November 17, 1990; phreatic eruptions after February 12, 1991, preceded by several weeks of volcanic tremor; phreatomagmatic eruptions after April 9, and dome effusion beginning May 19, 1991. This paper presents a hypothesis in which the top of the magma column rose about 20 m/day, reached the base of the water-saturated layer at the end of January, 1991, and approached the upper boundary of this layer on April 9. Thus, the temporal change of eruption type and associated phenomena are systematically explained by an interaction between magma and groundwater contained in the saturated layer.  相似文献   
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In this study we analyzed the chemical composition of hydrothermally altered dacite and basalt from the Kuroko mining area, northeastern Honshu, Japan, by REE (rare earth element). Features of rare earth element analyses include: (1) altered footwall dacite exhibits a negative Eu anomaly compared with fresh dacite, suggesting preferential removal of Eu2+ from the altered dacite via hydrothermal solutions, (2) altered hangingwall dacite and basalt and dacite and basalt adjacent to ore deposits exhibit positive Eu anomalies compared with fresh dacite and basalt, suggesting addition of Eu2+ from hydrothermal solutions, (3) LREE ratio (∑LREE/∑REE) from altered dacite of chlorite–sericite zone and K-feldspar zone show a negative relationship with δ18O, and La/Sm ratios show a positive correlation with the K2O index. These trends indicate the addition of light rare earth elements such as La to the altered dacite from hydrothermal solution and/or leaching of heavy rare earth elements such as Sm and Yb, (4) Principal component analysis (PCA) indicates that light rare earth elements enrichment is related to the formation of sericite zone near the Kuroko deposits but not to the formations of chlorite and K-feldspar zones, and (5) The correlations among REE features (LREE ratio, MREE ratio, HREE ratio, Eu/Eu?), δ18O and K2O index are not found for montmorillonite zone, mixed layer clay mineral zone and mordenite zone. Therefore, it is inferred that sericite, chlorite and K-feldspar alterations are related to the Kuroko and vein-type mineralization, but montmorillonite and mordenite alterations are not related to the mineralizations, and probably they formed at the post-mineralization stage.  相似文献   
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Basalt in the Furutobe District of the Kuroko mine area in Japan is characterized by abundant chlorite and epidote. Fluid inclusion studies indicate that chlorite is formed at lower temperatures (230–250°C) than epidote (250–280°C). The seawater/basalt mass ratio for the early chlorite-rich alteration was high (max. 40), but that for the later alteration was low (0.1–1.8). The CaO, Na2O and SiO2 of the bulk rock correlate negatively with MgO, while FeO and Σ Fe correlate positively with MgO. These changes in the characteristic features of hydrothermal alteration from early to late are generally similar to those for a mid-ocean ridge geothermal system accompanying basalt alteration.The MgO/FeO ratios of chlorite and actinolite and the Fe2O3 concentration of epidote from the basalt are greater than those of mid-ocean ridge basalt probably owing to the differences in the Fe2O3/FeO and MgO/FeO ratios of the parent rocks. The lower CaO concentration and the higher Na2O concentration of the bulk rock compared with altered mid-ocean ridge basalt can be interpreted in terms of the difference in original bulk rock compositions.The Furutobe basalt, as well as other submarine back arc basalts, contains more vesicles filled with hydrothermal minerals (epidote, calcite, quartz, chlorite, pyrite) than do the mid-ocean ridge basalts. The abundance of vesicles plays an important role in controlling the secondary mineralogy and geochemistry of hydrothermally altered submarine back arc basin basalts.  相似文献   
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Magnesite, siderite and dolomite are characteristic alteration minerals occurring in Miocene hanging wall rocks of dacitic composition which host the Kuroko orebodies. These carbonates generally occur in a more stratigraphically upper horizon than chlorite alteration zone surrounding the orebodies. The Mg/(Mg+Fe) ratios of the carbonates decrease from the central alteration zone to marginal zone. The Mg/(Mg+Fe) ratios of carbonates and chlorite positively correlate. The δ18O and δ13C values of magnesite, siderite and dolomite positively correlate with each other and lie between the igneous and marine carbonate values. The petrographic, isotopic and fluid inclusion characteristics and thermochemical modelling calculations indicate that magnesite and dolomite formed in the central zone close to the orebodies due to the interaction of hydrothermal solutions with the biogenic marine carbonates. Calcite formed further from the orebodies from hydrothermal fluids which did not contain a biogenic marine carbon component. The compositional and textural relationships indicate that superimposed alterations (chlorite alteration and carbonate alteration) occurred in hanging wall rocks. The mode of occurrences and the Mg/(Mg+Fe) ratios of magnesite and dolomite occurring in hanging wallrocks are useful in the exploration for concealed volcanogenic massive sulfide-sulfate deposits. Received: 9 September 1997 / Accepted: 23 September 1997  相似文献   
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From July to November 1988, a major electromagnetic (EM) experiment, known as EMRIDGE, took place over the southern end of the Juan de Fuca Ridge in the northeast Pacific. It was designed to complement the previous EMSLAB experiment which covered the entire Juan de Fuca Plate, from the spreading ridge to subduction zone. The principal objective of EMRIDGE was to use natural sources of EM induction to investigate the processes of ridge accretion. Magnetotelluric (MT) sounding and Geomagnetic Depth Sounding (GDS) are well suited to the study of the migration and accumulation of melt, hydrothermal circulation, and the thermal evolution of dry lithosphere. Eleven magnetometers and two electrometers were deployed on the seafloor for a period of three months. Simultaneous land-based data were made available from the Victoria Magnetic Observatory, B.C., Canada and from a magnetometer sited in Oregon, U.S.A.Changes in seafloor bathymetry have a major influence on seafloor EM observations as shown by the orientation of the real GDS induction arrows away from the ridge axis and towards the deep ocean. Three-dimensional (3D) modelling, using a thin-sheet algorithm, shows that the observed EM signature of the Juan de Fuca Ridge and Blanco Fracture Zone is primarily due to nonuniform EM induction within the ocean, associated with changes in ocean depth. Furthermore, if the influence of the bathymetry is removed from the observations, then no significant conductivity anomaly is required at the ridge axis. The lack of a major anomaly is significant in the light of evidence for almost continuous hydrothermal venting along the neo-volcanic zone of the southern Juan de Fuca Ridge: such magmatic activity may be expected to have a distinct electrical conductivity signature, from high temperatures, hydrothermal fluids and possible melt accumulation in the crust.Estimates of seafloor electrical conductivity are made by the MT method, using electric field records at a site 35 km east of the ridge axis, on lithosphere of age 1.2 Ma, and magnetic field records at other seafloor sites. On rotating the MT impedance tensor to the principal axis orientation, significant anisotropy between the major (TE) and minor (TM) apparent resistivities is evident. Phase angles also differ between the principal axis polarisations, and TM phase are greater than 90° at short periods. Thin-sheet modelling suggests that bathymetric changes accounts for some of the observed 3D induction, but two-dimensional (2D) electrical conductivity structure in the crust and upper mantle, aligned with the ridge axis, may also be present. A one-dimensional (1D) inversion of the MT data suggests that the top 50 km of Earth is electrically resistive, and that there is a rise in conductivity at approximately 300 km. A high conductivity layer at 100 km depth is also a feature of the 1D inversion, but its presence is less well constrained.  相似文献   
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The Tono sandstone-type uranium mine area, middle Honsyu, Japan is composed of Miocene lacustrine sedimentary rocks in the lower part (18–22 Ma) and marine facies in the upper part (15–16 Ma). Calcite and pyrite occur as dominant diagenetic alteration products in these Neogene sedimentary rocks. The characteristics of calcite and pyrite differ significantly between lacustrine and marine facies. Abundant pyrite, calcite, organic matter, and small amounts of marcasite or pyrrhotite occur in the lacustrine facies, whereas small amounts of calcite and framboidal pyrite, organic matter and no marcasite or pyrrhotite are found within the marine units. The δ13C values of calcite in the lacustrine deposits are low (−19 to −6‰ PDB) but those in marine formation are high (−11 to +3‰). This implies that the contribution of marine carbonate is larger in upper marine sedimentary rocks, and carbon in calcite in the lower lacustrine formation was derived both from oxidation of organic matter and from dissolved marine inorganic carbon. The δ34S values of framboidal pyrite in the upper marine formation are low (−14 to −8‰ CDT), indicating a small extent of bacterial seawater sulfate reduction, whereas those of euhedral-subhedral pyrite in the lower lignite-bearing arkose sandstone are high (+10 to +43‰), implying a large extent of closed-system bacterial seawater sulfate reduction. The δ34S and δ13C data which deviate from a negative correlation line toward higher δ13C values suggest methanogenic CO2 production. During diagenesis of the lacustrine unit, large amounts of euhedral-subhedral pyrite were formed, facilitated by extensive bacterial reduction of seawater sulfate with concomitant oxidation of organic matter, and by hydrolysis reactions of organic matter, producing CH4 and CO2. Uranium minerals (coffinite and uraninite) were also formed at this stage by the reduction of U6+ to U4+. The conditions of diagenetic alteration within the lacustrine deposits and uranium mineralization is characterized by low Eh in which nearly equal concentrations of CH4 and HCO3 existed and reduced sulfur species (H2S, HS) are predominant among aqueous sulfur species, whereas diagenetic alteration of the marine formations was characterized by a predominance of SO4 2− among dissolved sulfur species. Modern groundwater in the lacustrine formation has a low Eh value (−335 mV). Estimated and measured low Eh values of modern and ancient interstitial waters in lacustrine environments indicate that a reducing environment in which U4+ is stable has been maintained since precipitation of uranium minerals. Received: 9 February 1996 / Accepted: 11 April 1997  相似文献   
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