Magnetotelluric Investigation of the Hydrothermal System and Heat Source in the Muine-Toyoha Geothermal Area, Hokkaido, Japan

Abstract. Magnetotelluric (MT) surveys were carried out around the Muine volcano, Hokkaido, Japan, where it is expected that the heat and metal source forming the polymetallic Ag-Pb-Zn-Cu-In Toyoha deposit is present at depth. Measurements were performed at 20 sites, 18 of which were located along a WSW-ENE profile traversing the north ridge of Mt. Muine. A resistivity model obtained from 2D inversion of the MT data shows subsurface specific conductive and resistive features. Conductive layers are present at the surface of Mt. Muine. The low resistivity is probably due to the clay-rich rocks associated with the hydrothermal alteration. A high resistivity layer, which corresponds to the pre-Tertiary Usubetsu Formation, crops out east of Mt. Muine and dips westward. At the west foot of Mt. Muine, relatively high resistive layers are widely exposed. The resistivity increases with depth and exceeds 1000 ohm-m. This fact indicates that this region is not influenced by the recent hydrothermal activity. An extremely conductive zone about 3–6 km wide and 6–9 km thick exists at a depth of 2 km below Mt. Muine. This zone mostly corresponds to an elastic wave attenuation zone detected by a seismic survey. It is interpreted as a large hydrothermal reservoir or melted magma, which is a heat source of the hydrothermal system in this area.     

Methane in the East China Sea water

Methane in the East China Sea water was determined four times at a fixed vertical section along PN line consisting of 11–14 stations, in February 1993, October 1993, June 1994 and August 1994. The mean concentration of methane in the surface water was not significantly higher than that in the open ocean. The methane concentration below the pycnocline increased during the stratified period in summer to autumn and reached to 15 nmoles/l at most in October. The concentration of methane was fairly well correlated with AOU in the layer below the pycnocline in the stratified season. This means that methane in the bottom water has only a single source, which is expected to be anoxic sediments near the coast, and that the oxidation rate of methane in the water is extremely slow in the oxic water. The high methane observed in October completely disappeared in February, indicating that the methane was escaped to the atmosphere or transported to the pelagic ocean by the Kuroshio current. The East China Sea, therefore, is not a large direct and stationary source for the atmospheric methane, but may have some role as a source by supplying it sporadically to the atmosphere in early winter or indirectly from the surface of the pelagic ocean.     

Annual variation of methane in seawater in Funka bay,Japan

The concentration of methane in seawater was determined approximately once a month for one year from August 1990 to July 1991 at a station close to the center of Funka bay (92 m depth) and some supplementary observations were also carried out. The concentration of methane was usually increased with increasing depth, suggesting that methane was emitted from the bottom of the bay. While highly variable both spatially and temporally, the emission was intense in March and April, a period immediately after the spring bloom of phytoplankton. The maximum of methane found in the intermediate water suggests its source from the slope of the bay. The concentration of methane in the surface water changed seasonally and also interannually. The annually averaged flux of methane transferred to the atmosphere in the bay was estimated to be 6×10^–3 gCH₄m²/day. The coastal zone in the world may be a significant source of the atmospheric methane, although its source strength has yet to be accurately estimated from more data in different coastal seas.     

Raman spectroscopic and calorimetric observations on natural gas hydrates with cubic structures I and II obtained from Lake Baikal

This study reports measurements of the Raman spectra of Lake Baikal gas hydrates and estimations of the hydration number of methane-rich samples. The hydration number of gas hydrates retrieved from the southern Baikal Basin (crystallographic structure I) was approx. 6.1. Consistent with previous results, the Raman spectra of gas hydrates retrieved from the Kukuy K-2 mud volcano in the central Baikal Basin indicated the existence of crystallographic structures I and II. Measurements of the dissociation heat of Lake Baikal gas hydrates by calorimetry (from the decomposition of gas hydrates to gas and water), employing the hydration number, revealed values of 53.7–55.5?kJ?mol^–1 for the southern basin samples (structure I), and of 54.3–55.5?kJ?mol^–1 for the structure I hydrates and 62.8–64.2?kJ?mol^–1 for the structure II hydrates from the Kukuy K-2 mud volcano.     

Short time scales of magma-mixing processes prior to the 2011 eruption of Shinmoedake volcano, Kirishima volcanic group, Japan

We estimated time scales of magma-mixing processes just prior to the 2011 sub-Plinian eruptions of Shinmoedake volcano to investigate the mechanisms of the triggering processes of these eruptions. The sequence of these eruptions serves as an ideal example to investigate eruption mechanisms because the available geophysical and petrological observations can be combined for interpretation of magmatic processes. The eruptive products were mainly phenocryst-rich (28 vol%) andesitic pumice (SiO₂ 57 wt%) with a small amount of more silicic pumice (SiO₂ 62–63 wt%) and banded pumice. These pumices were formed by mixing of low-temperature mushy silicic magma (dacite) and high-temperature mafic magma (basalt or basaltic andesite). We calculated the time scales on the basis of zoning analysis of magnetite phenocrysts and diffusion calculations, and we compared the derived time scales with those of volcanic inflation/deflation observations. The magnetite data revealed that a significant mixing process (mixing I) occurred 0.4 to 3 days before the eruptions (pre-eruptive mixing) and likely triggered the eruptions. This mixing process was not accompanied by significant crustal deformation, indicating that the process was not accompanied by a significant change in volume of the magma chamber. We propose magmatic overturn or melt accumulation within the magma chamber as a possible process. A subordinate mixing process (mixing II) also occurred only several hours before the eruptions, likely during magma ascent (syn-eruptive mixing). However, we interpret mafic injection to have begun more than several tens of days prior to mixing I, likely occurring with the beginning of the inflation (December 2009). The injection did not instantaneously cause an eruption but could have resulted in stable stratified magma layers to form a hybrid andesitic magma (mobile layer). This hybrid andesite then formed the main eruptive component of the 2011 eruptions of Shinmoedake.     

Molecular and isotopic characteristics of gas hydrate-bound hydrocarbons in southern and central Lake Baikal

We investigated the molecular composition (methane, ethane, and propane) and stable isotope composition (methane and ethane) of hydrate-bound gas in sediments of Lake Baikal. Hydrate-bearing sediment cores were retrieved from eight gas seep sites, located in the southern and central Baikal basins. Empirical classification of the methane stable isotopes (δ¹³C and δD) for all the seep sites indicated the dominant microbial origin of methane via methyl-type fermentation; however, a mixture of thermogenic and microbial gases resulted in relatively high methane δ¹³C signatures at two sites where ethane δ¹³C indicated a typical thermogenic origin. At one of the sites in the southern Baikal basin, we found gas hydrates of enclathrated microbial ethane in which ¹³C and deuterium were both highly depleted (mean δ¹³C and δD of –61.6‰ V-PDB and –285.4‰ V-SMOW, respectively). To the best of our knowledge, this is the first report of C₂ δ¹³C–δD classification for hydrate-bound gas in either freshwater or marine environments.     

Noble gases in ureilites released by crushing

Abstract— Noble gases in two ureilites, Kenna and Allan Hills (ALH) 78019, were measured with two extraction methods: mechanical crushing in a vacuum and heating. Large amounts of noble gases were released by crushing, up to 26.5% of ¹³²Xe from ALH 78019 relative to the bulk concentration. Isotopic ratios of the crush‐released Ne of ALH 78019 resemble those of the trapped Ne components determined for some ureilites or terrestrial atmosphere, while the crush‐released He and Ne from Kenna are mostly cosmogenic. The crush‐released Xe of ALH 78019 and Kenna is similar in isotopic composition to Q gas, which indicates that the crush‐released noble gases are indigenous and not caused by contamination from terrestrial atmosphere. In contrast to the similarities in isotopic composition with the bulk samples, light elements in the crush‐released noble gases are depleted relative to Xe and distinct from those of each bulk sample. This depletion is prominent especially in the ²⁰Ne/¹³²Xe ratio of ALH 78019 and the ³⁶Ar/¹³²Xe ratio of Kenna. The values of measured ³He/²¹Ne for the gases released by crushing are significantly higher than those for heating‐released gases. This suggests that host phases of the crush‐released gases might be carbonaceous because cosmogenic Ne is produced mainly from elements with a mass number larger than Ne. Based on our optical microscopic observation, tabular‐foliated graphite is the major carbon mineral in ALH 78019, while Kenna contains abundant polycrystalline graphite aggregates and diamonds along with minor foliated graphite. There are many inclusions at the edge and within the interior of olivine grains that are reduced by carbonaceous material. Gaps can be seen at the boundary between carbonaceous material and silicates. Considering these petrologic and noble gas features, we infer that possible host phases of crush‐released noble gases are graphite, inclusions in reduction rims, and gaps between carbonaceous materials and silicates. The elemental ratios of noble gases released by crushing can be explained by fractionation, assuming that the starting noble gas composition is the same as that of amorphous carbon in ALH 78019. The crush‐released noble gases are the minor part of trapped noble gases in ureilites but could be an important clue to the thermal history of the ureilite parent body. Further investigation is needed to identify the host phases of the crush‐released noble gases.     

Convection induced by cooling at one side wall in two-dimensional non-rotating fluid —applicability to the deep Pacific circulation—

In recognition that similarity in the density balance leads to resemblance in circulation between the two-dimensional non-rotating and three-dimensional rotating systems which have similar density stratification, we investigate convection induced by cooling at one side wall and heating at the sea surface by using a two-dimensional non-rotating model as idealized representation for the deep Pacific circulation. In the model, various vertical profiles are taken for the side wall cooling, which are assumed to correspond to the density structure of the Anatarctic Circumpolar Current. In a small diffusivity range, two important features are found to be robust against change in the vertical profile of the side wall cooling. One is that the density stratification is horizontally almost uniform. The other is that the balance in the density equation between the vertical advection and the vertical diffusion holds in the interior. Consequently, the vertical density balance, together with the equation of continuity, determines the circulation pattern for the prescribed vertical profile of the side wall cooling. The multi-layered meridional flow, which is expected to exist in the deep Pacific, is shown to form for certain vertical profiles of the side wall cooling.     

Effects of bottom topography and density stratification on the formation of western boundary currents

A wind-driven, general circulation for a two-layer ocean with continental shelf-slope along the western boundary is studied numerically. Special attention is focused on the formation process of the western boundary current in the subtropical gyre. The western boundary current develops in the upper layer along the western boundary on the shelf-slope with a bottom trapped poleward flow in the lower layer. The poleward undercurrent is concentrated approximately along the contour lines of the potential vorticity,f/D, wheref is the Coriolis parameter andD the depth of the ocean. The separation of upper- and lower-layer flows on the shelf-slope represents a typical transient response. As the response approaches a steady state, the poleward undercurrent decreases in amplitude, and the motion tends to be confined to the upper layer. The flow pattern becomes similar to that found in a flat bottom ocean. A steady-state response is expected to be isostatic (no motion in the lower layer), even on the shelf-slope, as conservation of potential vorticity would suggest.The remarkable increase in transport of the western boundary current produced by the formation of an anticyclonic vortex on the shelf-slope extending throughout the hemisphere (Holland, 1973) does not occur in the wind-driven general circulation.     

Source models for the 1993 Hokkaido Nansei-Oki earthquake tsunami

A source model for the 1993 Hokkaido Nansei-Oki tsunami must satisfy certain conditions. Such conditions are presented in this paper, and two methods are used to determine the best source model for this event. A trial-and-error method selects DCRC-17a as the best among 24 different models. This model has three fault planes dipping westward. To reproduce well the tide gauge records at two locations, an inversion analysis is used to modify the dislocation of DCRC-17a.