Phase relation of CaSO<Subscript>4</Subscript> at high pressure and temperature up to 90 GPa and 2300 K

Calcium sulfate (CaSO₄), one of the major sulfate minerals in the Earth’s crust, is expected to play a major role in sulfur recycling into the deep mantle. Here, we investigated the crystal structure and phase relation of CaSO₄ up to ~90 GPa and 2300 K through a series of high-pressure experiments combined with in situ X-ray diffraction. CaSO₄ forms three thermodynamically stable polymorphs: anhydrite (stable below 3 GPa), monazite-type phase (stable between 3 and ~13 GPa) and barite-type phase (stable up to at least 93 GPa). Anhydrite to monazite-type phase transition is induced by pressure even at room temperature, while monazite- to barite-type transition requires heating at least to 1500 K at ~20 GPa. The barite-type phase cannot always be quenched from high temperature and is distorted to metastable AgMnO₄-type structure or another modified barite structure depending on pressure. We obtained the pressure–volume data and density of anhydrite, monazite- and barite-type phases and found that their densities are lower than those calculated from the PREM model in the studied P–T conditions. This suggests that CaSO₄ is gravitationally unstable in the mantle and fluid/melt phase into which sulfur dissolves and/or sulfate–sulfide speciation may play a major role in the sulfur recycling into the deep Earth.     

Comparative assessment of Japan's long-term carbon budget under different effort-sharing principles

This article assesses Japan's carbon budgets up to 2100 in the global efforts to achieve the 2?°C target under different effort-sharing approaches based on long-term GHG mitigation scenarios published in 13 studies. The article also presents exemplary emission trajectories for Japan to stay within the calculated budget.

The literature data allow for an in-depth analysis of four effort-sharing categories. For a 450?ppm CO₂e stabilization level, the remaining carbon budgets for 2014–2100 were negative for the effort-sharing category that emphasizes historical responsibility and capability. For the other three, including the reference ‘Cost-effectiveness’ category, which showed the highest budget range among all categories, the calculated remaining budgets (20th and 80th percentile ranges) would run out in 21–29 years if the current emission levels were to continue. A 550?ppm CO₂e stabilization level increases the budgets by 6–17 years-equivalent of the current emissions, depending on the effort-sharing category. Exemplary emissions trajectories staying within the calculated budgets were also analysed for ‘Equality’, ‘Staged’ and ‘Cost-effectiveness’ categories. For a 450?ppm CO₂e stabilization level, Japan's GHG emissions would need to phase out sometime between 2045 and 2080, and the emission reductions in 2030 would be at least 16–29% below 1990 levels even for the most lenient ‘Cost-effectiveness’ category, and 29–36% for the ‘Equality’ category. The start year for accelerated emissions reductions and the emissions convergence level in the long term have major impact on the emissions reduction rates that need to be achieved, particularly in the case of smaller budgets.

Policy relevance

In previous climate mitigation target formulation processes for 2020 and 2030 in Japan, neither equity principles nor long-term management of cumulative GHG emissions was at the centre of discussion. This article quantitatively assesses how much more GHGs Japan can emit by 2100 to achieve the 2?°C target in light of different effort-sharing approaches, and how Japan's GHG emissions can be managed up to 2100. The long-term implications of recent energy policy developments following the Fukushima nuclear disaster for the calculated carbon budgets are also discussed.     

Temporal variations in the current structure and volume transport of the Coastal Oyashio revealed by direct current measurement

Direct current measurements by a shipboard and bottom-mounted acoustic Doppler current profiler and concurrent hydrographic observations with a CTD were conducted off southeastern Hokkaido, Japan, between January and May 2005 to reveal temporal variations in the current structure and volume transport of the Coastal Oyashio (CO). The CO, which has a baroclinic jet structure with southwestward speeds exceeding 90 cm s^?1 and a width of 7–8 km, was associated with a surface-to-bottom density front and was formed on the offshore side of the shelf break. The volume transport of CO (T _CO) was estimated by integrating the fluxes of lower-density water that was trapped against the coast along the density front represented by the 26.2 σ _θ isopycnal line. This transport decreased monotonously from 0.79 Sv (1 Sv = 10⁶ m³ s^?1) in January to 0.21 Sv in March and subsequently to 0.12 Sv in May, possibly due to the decay of the East Sakhalin Current Water in the Okhotsk Sea. Accompanied by a decrease in T _CO, the location of the jet structure associated with the density front moved toward the coast while the maximum speed of the jet decreased and the tilt of the front became more horizontal. Consequently, more saline offshore Oyashio water flowed into the deep part of the shelf area, and the current structure altered from relatively barotropic in winter to baroclinic in spring. This study is the first to estimate the observed volume transport of the CO from direct current measurements.     

The Nature of Mantle Rocks in Ophiolites of the Polar Urals

This work presents the results of geochemical (LA-ICP-MS) study of minerals of peridotites from ophiolite complexes of the Polar Urals to clarify the nature of these formations. The distribution of trace and rare earth elements in clinopyroxenes testifies that there were three types of the mantle substratum, which formed in different geodynamic settings. Two types of primary peridotites were formed upon partial melting of the mantle at different-depth levels in the subduction zone. The first type is represented by lherzolites and diopside harzburgites, formed at partial melting under the spinel facies conditions; the second type is represented by diopside harzburgites, formed under polybaric partial melting under the garnet and spinel facies conditions. In the suprasubduction zone, peridotites experienced fluid-induced partial melting that resulted in crystallization of harzburgites. All types of harzburgites were transformed by ascending melts and fluids (refertilization) and high-temperature hydration with the formation of amphibole. These processes are recorded in variations in the REE spectra of minerals.     

Do sedentary behavior and physical activity spatially cluster? Analysis of a population-based sample of Boston adolescents

Sedentary behavior and lack of physical activity are key modifiable behavioral risk factors for chronic health problems, such as obesity and diabetes. Little is known about how sedentary behavior and physical activity among adolescents spatially cluster. The objective was to detect spatial clustering of sedentary behavior and physical activity among Boston adolescents. Data were used from the 2008 Boston Youth Survey Geospatial Dataset, a sample of public high school students who responded to a sedentary behavior and physical activity questionnaire. Four binary variables were created: (1) TV watching (>2 h/day), (2) video games (>2 h/day), (3) total screen time (>2 h/day); and (4) 20 min/day of physical activity (≥5 days/week). A spatial scan statistic was utilized to detect clustering of sedentary behavior and physical activity. One statistically significant cluster of TV watching emerged among Boston adolescents in the unadjusted model. Students inside the cluster were more than twice as likely to report >2 h/day of TV watching compared to respondents outside the cluster. No significant clusters of sedentary behavior and physical activity emerged. Findings suggest that TV watching is spatially clustered among Boston adolescents. Such findings may serve to inform public health policy-makers by identifying specific locations in Boston that could provide opportunities for policy intervention. Future research should examine what is linked to the clusters, such as neighborhood environments and network effects.     

Potential of mosques to serve as evacuation shelters for foreign Muslims during disasters: a case study in Gunma,Japan

Natural Hazards - Foreigners tend to be vulnerable to disasters due to religious and cultural differences. In Japan, Muslim foreign residents, who are minorities, likely face difficulties in terms...     

Global assessment of the effectiveness of adaptation in coastal areas based on RCP/SSP scenarios

Climatic Change - The objective of this study is to assess the global impact of sea level rise and to evaluate the effectiveness of adaptation. Global areas of inundation due to sea level rise are...     

Geochemistry of newly discovered quaternary Shiribeshi Volcano,Northeast Japan Sea

Summary Shiribeshi Seamount is located to the east of the Okushiri Ridge, in the northeast Japan Sea. Whole rock K-Ar age of olivine-augite andesite dredged from the Seamount was determined to be 0.9 ± 0.2 Ma (Tsuchiya et al., 1989), indicating that Shiribeshi Seamount is a Quaternary volcano in the back-arc region off the junction of the Northeast Japan and Kurile arcs. Shiribeshi volcano is composed of basalt to rhyolite, which show a typical island arc calc-alkaline nature on the basis of petrographical characteristics of 95 samples dredged from four sites. Abundances of incompatible elements including K, Rb, Sr, Nb, P, Ti, Y and Zr in 16 representative rocks are discussed, together with those in the Quaternary volcanic rocks from the NE Japan and Kurile arcs in terms of compositional variation across the arcs. The estimated composition of the primary magma of Shiribeshi volcano is characterized by higher incompatible element contents and a higher Zr/Y ratio than primary magmas in the volcanic front side. Based on HFS element concentrations the degree of partial melting for three primary magmas of Oshima-Oshima, Shiribeshi and Rishiri volcanoes in the northeast Japan Sea may decrease gradually with increasing distance from the volcanic front. However, LIL element contents, especially K and Rb are lower in the primary magma of Rishiri volcano located far from the volcanic front than in the remaining two primary magmas, which would imply that LIL/HFS ratios (or degree of contribution of LIL elements originating from the subducted oceanic crust) become minimal at Rishiri volcano. One basalt and three andesites from Shiribeshi volcano have the restricted range of low⁸⁷Sr/⁸⁶Sr ratios of 0.70297–0.70300, which indicates that the magma source for Shiribeshi volcano may be slightly more enriched in Sr isotopic compositions than theN-type MORB source.

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Geochemie des neuentdeckten quartären submarinen Vulkans Shiribeshi im Nordöstlichen Japanischen Meer

Zusammenfassung Der Shiribeshi Seamount liegt östlich des Okushiri Rückens im nordöstlichen Japanischen Meer. Gesamtgesteins K-Ar Alter von Olivin-Augit-Andesiten von diesem Seamount ergeben Werte von 0,9 ± 0,2 Ma (Tsuchiya et al., 1989), und weisen darauf hin, daß Shiribeshi ein quartärer Vulkan im back-arc Bereich nahe dem Kreuzungspunkt des nordostjapanischen und des Kurilen-Inselbogens ist. Er besteht aus Gesteinen, deren Zusammensetzung von Basalt bis Rhyolit reicht. Petrographische Daten von 25 Proben, die von vier submarinen Lokationen durch Dredging aufgesammelt wurden, weisen auf eine typische kalk-alkalische Inselbogenzusammensetzung hin. Die Verbreitung von inkompatiblen Elementen, die unter anderem K, Rb, Sr, Nb, P, Ti, Y und Zr umfassen, in 16 representativen Proben wird zusammen mit denen von quartären vulkanischen Gesteinen aus dem nordöstlichen Japanischen und den Kurilen-Inselbogen diskutiert; dabei wird Variationen der Zusammensetzung über die Bögen hinweg besondere Beachtung geschenkt. Die so ermittelte Zusammensetzung des primären Magmas des Shiribeshi Vulkans wird durch höhere inkompatible Elementgehalte und höhere Zr/Y Verhältnisse charakterisiert, wenn man sie mit primären Magmen an der vulkanischen Stirn des Inselbogens vergleicht. HFS Element-Konzentrationen lassen erkennen, daß der Grad teilweiser Aufschmelzung für drei primäre Magmen von Oshima-Oshima, Shiribeshi und Rishiri im nordöstlichen Japanischen Meer graduell mit zunehmender Entfernung von der vulkanischen Stirm abnimmt. Die Gehalte an LIL Elementen und besonders an K und Rb sind in dem primären Magma des Rishiri Vulkans, der weit von der vulkanischen Front entfernt liegt, höher als in den zwei anderen primären Magmen. Dies weist darauf hin, daß LIL/HFS Verhältnisse (oder der Beitrag von LIL Elementen, die aus subduzierter ozeanischer Kruste stammen) am Rishiri Vulkan ein Minimum erreichen. Ein Basalt und drei Andesite von Shiribeshi zeigen⁸⁷Sr/⁸⁶Sr Verhältnisse von 0,70297 bis 0,70300; dies läßt erkennen, daß die Quelle des Magmas für Shiribeshi etwas mehr an⁸⁷Sr angereichert war, als dieN-Typ Quelle.

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With 7 Figures     

Antiferromagnetic transition of fayalite under high pressure studied by Mössbauer spectroscopy

Néel temperature (Tm _N of α-Fe₂SiO₄ (fayalite) was measured as a function of pressure by means of Mössbauer spectroscopy in the pressure range 0–16 Gpa. High pressure was generated using a clamp-type miniature diamond anvil cell which was inserted into a cryostat. The Néel temperature increased linearly with increasing pressure at a rate of dT _N /dp=2.2±0.2 K/GPa. The result is discussed on the basis of the model proposed for the magnetic structure of fayalite by Santoro et al. (1966). The observed dT _N /dp suggests that the superexchange interactions vary as the ?10/3 power of the volume while the volume dependence of the direct exchange interactions is positive and small.