Chemical monitoring of volcanic gas using remote FT-IR spectroscopy at several active volcanoes in Japan

Chemical compositions of volcanic gases of several Japanese active volcanoes have been monitored from distant safe places since the beginning of the 1990s using an FT-IR spectral radiometer. For absorption measurements, an infrared light source behind volcanic gas emissions is necessary in a volcanic environment. In the early observations, infrared radiation from hot lava domes (Unzen volcano) and hot ground heated by high-temperature fumaroles (Usu, Aso, and Satsuma-Iwojima volcanoes) were used as infrared light sources. However, these sources were not available in many cases. This remote FT-IR method became more commonly applied to chemical monitoring of volcanic gases emitted from the summit or slopes of active volcanoes using scattered solar infrared light as infrared light sources (Sakurajima, Miyakejima, and Asama volcanoes). To date, eight species have been measured using this method: SO₂, HCl, HF, CO, CO₂, COS, SiF₄, and H₂O. The observations indicate that volcanic gases for each volcano have different chemical composition on a SO₂–HCl–HF ternary diagram in spite of similar tectonic settings, suggesting that vapor/melt volume ratios during volcanic gas formation differ among volcanoes. During more than 15 years of monitoring, chemical changes in volcanic gases attributable to ascent of magma were observed only at Asama, where HCl/SO₂ and HF/HCl ratios in the eruptive period were higher than those in non-eruptive period because of scrubbing of more soluble components in surface hydrothermal systems in the non-eruptive stage or solubility-controlled fractionation processes. Results show that these parameters are the most prospective ones among the various parameters measured using the remote FT-IR method to monitor volcanic activities.     

The geochemistry of volatile species in melt inclusions and sulfide minerals from Izu-Oshima volcano, Japan

Olivine-hosted melt inclusions in the O95 pyroclastic layer of Izu-Oshima volcano, Japan are basaltic to basaltic-andesitic in composition. The negative correlation between SiO₂ and H₂O in melt inclusions and reverse compositional zoning observed in olivine and other mineral phenocrysts is inferred to arise from mixing between a highly evolved and a less evolved magma. The latter is characterized by the highest S (0.15 wt.%) and H₂O (3.4 wt.%) concentrations among those described in reports of previous studies. The S⁶⁺/S_total ratios in melt inclusions were 0.64?–?0.73, suggesting a relatively high oxidation state (NNO + 0.87 at 1150°C). The presence of pyrrhotites, which are found only in titanomagnetite microlites, suggests that sulfide saturation occurred during microlite growth under at a sulfur fugacity (log fS₂) value of around + 0.5 for T = 1060°C. The groundmass glass compositions are more evolved (andesitic composition) than any melt inclusions containing high amounts of Cl (0.13 wt.%) but negligible H₂O (0.20 wt.%) and S (< 70 ppm), suggesting that Cl was retained in the magma, in contrast to S and H₂O, which degassed strongly during magma effusion.     

Effect of the variation in the lower tropospheric temperature on the wind onset of the Indian summer monsoon

There is a large thermal contrast between the Arabian Peninsula and India (Δθ _AI) at the mature stage of the Indian summer monsoon (ISM). The forming process of Δθ _AI is investigated analyzing various datasets. It forms earlier in the lower troposphere than in the middle and upper layers. The potential temperature in the lower troposphere over the west coast of India (θ _IW) abruptly decreases in advance of the rapid enhancement of the westerly wind over the Arabian Sea corresponding to the ISM onset. Such a process was observed for all the target years and the rapid decrease in θ _IW could trigger the ISM onset. The decrease in θ _IW had two patterns. In one case, cooler air is brought by the strong winds around a cyclone over the Arabian Sea. In another case, θ _IW decreases gradually by a synergy of a southwesterly wind over the Arabian Sea and the enlargement of Δθ _AI.     

Isotopic evidence for trapped fissiogenic REE and nucleogenic Pu in apatite and Pb evolution at the Oklo natural reactor

A part of the boundary layer of reactor zone 10 at the Oklo natural reactor shows a unique petrologic texture, which contains high-grade uraninite and massive apatite concretions. In order to study distribution behavior of fission products around the boundary between the reactor zone and the wall rock and to clarify the relation of migration mechanisms of fission products with geochemical factors, in-situ isotopic analyses of Nd, Sm, Gd, Pb and U in uraninite and apatite from the sample were performed by Sensitive High Resolution Ion Microprobe (SHRIMP). Sm and Gd isotopic ratios of uraninite and apatite show evidence of neutron irradiation with fluence between 4.4-6.8×10¹⁹ n/cm². Judging from the isotopic anomalies of Nd and U, the apatite coexisting with the uraninite plays an important role in trapping fissiogenic LREE and nucleogenic ²³⁹Pu into the structure. Systematic Pb isotopic data from apatite, uraninite, galena and minium suggest the following chronological interpretations.

1.

The apatite formed 1.92±0.01 Ga ago and trapped fissiogenic light REE and nucleogenic ²³⁹Pu that migrated from the reactor during the criticality.

2.

The uraninite around the boundary between reactor and sandstone dissolved once 1.1∼1.2 Ga ago.

3.

Galena grains were formed by U-Pb mobilization in association with the intrusion of dolerite dyke 0.45∼0.83 Ga ago.

4.

Minium was derived from recent dissolution of galena under locally oxidizing conditions.

     

Integrated description of deformation modes in a sedimentary basin: A case study around a shallow drilling site in the Mizunami area, eastern part of southwest Japan

Abstract   Tectonic episodes in a sedimentary basin are described on the basis of an integrated study combining reflection seismic interpretation, drilling survey and paleomagnetism. A shallow inclined borehole penetrated a fault shown by reflection seismic and geological surveys in the Mizunami area, in the eastern part of southwest Japan. Paleomagnetic measurements were carried out on core samples successfully oriented using side-wall image logging of structural attitude. At six horizons, stable characteristic remanent magnetization (ChRM) was confirmed through thermal and alternating field demagnetization tests, which were carried by magnetite with minor amounts of high coercivity minerals, as revealed by experiments of stepwise acquisition of isothermal remanent magnetization. After correction of multiphase deformation inferred from borehole structural analysis, ChRM directions were combined with previous data and confirmed an easterly deflection reflecting the coherent clockwise rotation of the arc before the Middle Miocene. Compilation of reliable paleomagnetic data described differential rotation of the eastern part of southwest Japan raised by collision of the Izu–Bonin Arc since the Middle Miocene. The present study suggests that (i) the Mizunami area is adjacent to a highly deformed zone bounded by the Akaishi Tectonic Line (ATL), and (ii) forearc deformation of southwest Japan is localized around the ATL, which is quite different from gradual bending on the back-arc side without remarkable crustal break related to the collision event.     

热液合成板状高结晶度三八面体蒙脱石

在热液条件下合成了板状的和高度结晶的三八面体蒙脱石。用淬冷玻璃与脱水的钠基蒙脱石分别在(a)500°C,100MPa下1天和11天;(b)300°C,100MPa下7天的条件下进行反应。产物的结晶度和颗粒大小取决于初始玻璃的化学组成,合成温度和热液改性的时间。XRD尖锐的峰和一定相对湿度下水合作用证明了产物结构的高度有序和大尺寸。透射电镜也被用来表征产物颗粒尺寸。通过改变初始材料的化学成分,产物的颗粒大小可以在10nm到几个微米之间变化。有序度最高和尺寸最大的产物是在500°C,100MPa的条件下用Na0.33(Mg1.83Al0.67)Si4O11成分的玻璃反应…     

Ion Chromatographic Determination of Fluorine and Chlorine in Silicate Rocks Following Alkaline Fusion

A simple and accurate method to determine fluorine and chlorine contents in small amounts (∼ 30 mg) in rock has been developed using ion chromatography after extraction by alkaline fusion. Powdered sample was mixed with sodium carbonate and zinc oxide at a mass ratio of 1:3:1, and was fused in an electric furnace at 900 °C for 30-40 minutes. An aqueous solution obtained by dissolving the fused silicate rock was diluted to the appropriate concentration of sodium carbonate (< ∼ 24 mmol l^-1) to minimise the tailing effect on F^- during ion chromatography caused by the large amount of carbonate species originating from the flux. Fluorine and chlorine contents were then determined by a standard additions method. Based on the relative standard deviation of the backgrounds, detection limits of both fluorine and chlorine were ∼ 4 μg g^-1, when 30 mg test portions were fused and diluted by a factor of 1200. We also report new fluorine and chlorine contents in nine GSJ (Geological Survey of Japan) reference materials, including peridotite (JP-1), granite (JG-1a), basalts (JB-1b, 2 and 3), andesites (JA-1 and 2) and rhyolites (JR-1 and 2). Fluorine and chlorine contents in the reference materials in this study were consistent with previously reported values. Reproducibilities were < 10 % for samples with F and Cl concentrations of > 20 μg g-1 and < 20 % with F and Cl < 20 μg g^-1.     

Magma mixing recorded in intermediate rocks associated with high-Mg andesites from the Setouchi volcanic belt, Japan: implications for Archean TTG formation

Calc-alkaline intermediate rocks are spatially and temporally associated with high-Mg andesites (HMAs, Mg#>60) in Middle Miocene Setouchi volcanic belt. The calc-alkaline rocks are characterized by higher Mg# (strongly calc-alkaline trend) than ordinary calc-alkaline rocks at equivalent silica contents. Phenocrysts in the intermediate rocks have petrographical features such as: (1) coexisting reversely and normally zoned orthopyroxene phenocrysts in single rock; (2) sieve type plagioclase in which cores are mantled by higher An%, melt inclusion-rich zone; and (3) reversely zoned amphibole phenocrysts with opacite cores. In addition, mingling textures and magmatic inclusions were observed in some rocks. These petrographic features and the mineral chemistry indicate that magma mixing was the most important process in producing the strongly calc-alkaline rocks. The core composition of normally zoned orthopyroxene phenocrysts and the mantle composition of reversely zoned orthopyroxene phenocrysts have relatively high Mg# (85–90) in maximum. Although basaltic and high-Mg andesitic magmas are candidate as possible mafic end-member magmas, basaltic magma is excluded in terms of phenocryst assemblage and bulk composition. HMA magmas are suitable mafic end-member magmas that precipitated high Mg# (90) orthopyroxene, whereas andesitic to dacitic magma are suitable felsic end-members. In contrast, it is difficult to produce the strongly calc-alkaline trend through fractional crystallization from a HMA magma, because it would require removal of plagioclase together with mafic minerals from the early stage of crystallization, whereas the precipitation of plagiolase is suppressed due to the high water content of HMA magmas. These results imply that Archean Mg#-rich TTGs (>45–55), which are an analog of the strongly calc-alkaline rocks in terms of chemistry and magma genesis, can be derived from magma mixing in which a HMA magma is the mafic end-member magma, rather than by fractional crystallization from a HMA magma.     

Evaluation of tsunami impacts on shallow marine sediments: An example from the tsunami caused by the 2003 Tokachi-oki earthquake, northern Japan

A combined approach of field geology and numerical simulation was conducted for evaluating the tsunami impacts on the shelf sediments. The 2003 Tokachi-oki earthquake, M 8.0, that occurred on 25 September 2003 off southeastern Hokkaido, northern Japan, generated a locally destructive tsunami. Maximum run-up height of the tsunami waves reached 4 m above sea level. In order to estimate the tsunami impacts on shallow marine sediments, we compared pre- and post-tsunami marine sediments in water depths of 38–112 m in terms of grain size, sedimentary structure, and microfossil content. Decreases of fine fractions, especially finer than very fine sand, which led to coarsen the mean grain size, were detected in the inner shelf of the northern part of the study area. Foraminiferal assemblages also changed in the coarsened sediments. On the other hand, the other shelf sediments largely unchanged or slightly fined. We also simulated the tsunami wave velocity and direction, and grain size entrained by the modeled tsunami. The numerical simulation resulted in that the 2003 tsunami could transport very fine sand in water depths shallower than 45–95 m at the northern part of the study area. This is comparable with the actual grain-size changes after the tsunami had passed. However, some storms and tidal currents might also be possible to stir the surface sediments after the pre-tsunami survey, so we could not conclude that the grain-size changes had been caused only by the tsunami. Nevertheless, a combined approach of sampling and modeling was powerful for estimating the tsunami impacts under the sea.     

Kuroko and Hydrocarbon Deposits from Northern Honshu,Japan: A Possible Common Hydrothermal/Magmatic Origin?

Abstract. Northern Honshu is the most important area for mineral and oil resources in Japan. Many kuroko deposits and oil and gas fields are distributed in two belts along the northeast Japan arc, the kuroko metal‐belt on the Pacific side and the oil‐belt on the Sea of Japan side. The kuroko deposits are located mainly in the Green Tuff strata which formed as a result of submarine vol‐canism during the late Miocene and Pliocene. Most of the source rocks of the oil and gas deposits formed at the same time as the kuroko deposits and some of them are located in reservoirs of hydrothermally‐altered volcanic rocks in the Green Tuff region. There is general agreement that the kuroko deposits formed as a result of submarine hydrothermal and magmatic activity whereas almost all petroleum geologists and geochemists consider that hydrocarbon deposits were generated independently of such activity. Since the discovery of hydrothermally‐generated petroleum in the Guaymas Basin, Gulf of California, however, it is clear that petroleum can be formed almost instantaneously in terrestrial and submarine hydrothermal areas. The paleo‐northeastern Sea of Japan is therefore considered to be a potential area for hydrothermal petroleum generation because thick organic‐rich sediments overlie an active submarine volcanic area. Several lines of geological and geochemical evidence suggest the possibility of hydrothermally‐enhanced maturation of organic matter and the contribution of magmatic activity to the formation of these deposits. Although most of the oil and gas in northern Honshu has been generated conventionally as a consequence of the high geothermal gradients there, it appears that some of the oil and gas fields may have formed as a result of extensive hydrothermal and magmatic activity during the late Miocene to Pliocene. Because of the much steeper angle of the faults in the vicinity of the Hokuroku basin than in the Akita basin, the magmatic contribution to the kuroko mineralization would have been far greater than to the oil and gas deposits of the Niigata and Akita basins. We therefore propose a strong relationship between metal and oil and gas generation in northern Honshu based on the structure and tectonics of the northern Honshu arc‐backarc system.