Measurement of iodine-129 in seawater samples collected from the Japan Sea area using accelerator mass spectrometry: Contribution of nuclear fuel reprocessing plants

The concentrations of ¹²⁹I in seawater samples from two sites (off Sekine and the Toyama Bay) in the Japan Sea were determined by accelerator mass spectrometry. The observed concentrations exceed amounts expected from natural origin and globally distributed fallout due to nuclear weapons testing. Because the fraction of natural origin and global fallout is 2% and 8.9–13.8%, respectively, the residual more than 80% of the concentration must come primarily from nuclear fuel reprocessing plants. This result indicates a rapid distribution of ¹²⁹I through atmospheric transport on a global scale. The depth distribution of ¹²⁹I at the Toyama Bay in the Japan Sea shows that the ¹²⁹I maximum is in the mixed layer and that concentrations decrease with depth. The inventory of ¹²⁹I in water column is four times higher than that measured in the Gulf of Mexico which has almost the same depth at the Toyama Bay. This higher inventory probably reflects: (1) the rapid water sinking in the Japan Sea, (2) the difference of distance in sampling locations with respect to major ¹²⁹I releasing plants and (3) the strong increase in emissions from nuclear fuel reprocessing plants after the profile of the Gulf of Mexico was taken.     

Platinum–Group Minerals in Podiform Chromitite from the Kamuikotan Zone, Hokkaido, Northern Japan

Abstract: Ru–Os–Ir alloys have been found in two podiform chromitites located at the Chiroro and Bankei mines in the Sarugawa peridotite complex in the Kamuikotan zone, Hokkaido, Japan. This is the first report on the occurrence of PGM (= platinum-group minerals) from chromitites in Japan. The Ru–Os–Ir alloys most typically form polyhedra associated with other minerals (Ni–Fe alloys and heazlewoodite) in chromian spinel. The PGM are possibly pseudomorphs after some primary PGM such as laurite and are chemically highly inhomogeneous, indicating a low-temperature alteration origin. This is consistent with intense alteration (formation of serpentine, uvarovite and kämmererite) imposed on the Kamuikotan chromitites. High-temperature primary PGE (platinum–group elements)–bearing sulfides were possibly recrystallized at low temperatures into a new assemblage of PGM, Ni-Fe alloys and sulfides. Placer PGM around the peridotite complexes are chemically different from the PGM in dunite and chromitite possibly due to the, as yet, incomplete search for the rock-hosted PGM. The PGE content in chromitites is distinctly higher in those in the Kamuikotan zone than in those in the Sangun zone of Southwest Japan, consistent with the more refractory nature (Cr# of spinel, up to 0.8) of the former than the latter (Cr# of spinel, 0.5).     

Mantle peridotites from the Western Pacific

We review petrographical and petrological characteristics of mantle peridotite xenoliths from the Western Pacific to construct a petrologic model of the lithospheric mantle beneath the convergent plate boundary. The peridotite varies from highly depleted spinel harzburgite of low-pressure origin at the volcanic front of active arcs (Avacha of Kamchatka arc and Iraya of Luzon–Taiwan arc) to fertile spinel lherzolite of high-pressure origin at the Eurasian continental margin (from Sikhote-Alin through Korea to eastern China) through intermediate lherzolite–harzburgite at backarc side of Japan island arcs. Oxygen fugacity recorded by the peridotite xenoliths decreases from the frontal side of arc to the continental margin. The sub-arc type peridotite is expected to exist beneath the continental margin if accretion of island arc is one of the important processes for continental growth. Its absence suggests replacement by the continental lherzolite at the region of backarc to continental margin. Asthenospheric upwelling beneath the continental region, which has frequently occurred at the Western Pacific, has replaced depleted sub-cratonic peridotite with the fertile spinel lherzolite. Some of these mantle diapirs had opened backarc basins and strongly modified the lithospheric upper mantle by metasomatism and formation of Group II pyroxenites.     

A new type of orthopyroxenite xenolith from Takashima, Southwest Japan: silica enrichment of the mantle by evolved alkali basalt

We found fine-grained Fe-rich orthopyroxene-rich xenoliths (mainly orthopyroxenite) containing partially digested dunite fragments of Group I from Takashima, Southwest Japan. Orthopyroxenite veinlets, some of which contain plagioclase at the center, also replace olivine in dunite and wehrlite xenoliths of Group I. This shows high reactivity with respect to olivine of the melt involved in orthopyroxenite formation, indicating its high SiO₂ activity. The secondary orthopyroxene of this type is characterized by low Mg# [= Mg/(Mg + total Fe) atomic ratio] (down to 0.73) and high Al₂O₃ contents (5–6 wt%). It is different in chemistry from other secondary orthopyroxenes found in peridotite xenoliths derived from the mantle wedge. Clinopyroxenes in the Fe-rich orthopyroxenite show a convex-upward REE pattern with a crest around Sm. This pattern is strikingly similar to that of clinopyroxenes of Group II pyroxenite xenoliths and of phenocrystal and xenocrystal clinopyroxenes, indicating involvement of similar alkali basaltic melts. The Fe-rich orthopyroxenite xenoliths from Takashima formed by reaction between evolved alkali basalt melt and mantle olivine; alkali basalt initially slightly undersaturated in silica might have evolved to silica-oversaturated compositions by fractional crystallization at high-pressure conditions. The Fe-rich orthopyroxenites occur as dikes within the uppermost mantle composed of dunite and wehrlite overlying pockets of Group II pyroxenites. The orthopyroxene-rich pyroxenites of this type are possibly common in the uppermost mantle beneath continental rift zones where alkali basalt magmas have been prevalent.     

Isotopic composition of dissolved inorganic carbon in subsurface sediments of gas hydrate-bearing mud volcanoes, Lake Baikal: implications for methane and carbonate origin

We report on the isotopic composition of dissolved inorganic carbon (DIC) in pore-water samples recovered by gravity coring from near-bottom sediments at gas hydrate-bearing mud volcanoes/gas flares (Malenky, Peschanka, Peschanka 2, Goloustnoe, and Irkutsk) in the Southern Basin of Lake Baikal. The δ¹³C values of DIC become heavier with increasing subbottom depth, and vary between ?9.5 and +21.4‰ PDB. Enrichment of DIC in ¹³C indicates active methane generation in anaerobic environments near the lake bottom. These data confirm our previous assumption that crystallization of carbonates (siderites) in subsurface sediments is a result of methane generation. Types of methanogenesis (microbial methyl-type fermentation versus CO₂-reduction) were revealed by determining the offset of δ¹³C between dissolved CH₄ and CO₂, and also by using δ¹³C and δD values of dissolved methane present in the pore waters. Results show that both mechanisms are most likely responsible for methane generation at the investigated locations.     

Deep and Bottom Currents in the Challenger Deep,Mariana Trench,Measured with Super-Deep Current Meters

The bottom currents in the Challenger Deep, the deepest in the world, were measured with super-deep current meters moored at 11°22′ N and 142°35′ E, where the depth is 10915 m. Three current meters were set at 9687 m, 10489 m and 10890 m at the station in the center of the Challenger Deep for 442 days from 1 August 1995 to 16 October 1996. Although rotor revolutions in 60 minutes of recording interval were zero for 37.5% of the time, the maximum current at the deepest layer of 10890 m was 8.1 cm s⁻¹, being composed of tidal currents, inertia motion and long period variations. Two current meters were set at 6608 m and 7009 m at a station 24.9 km north of the center for 443 days from 31 July 1995 to 16 October 1996, and two current meters at 6214 m and 6615 m at a station 40.9 km south of the center for 441 days from 2 August 1995 to 16 October 1996. The mean flow at 7009 m depth at the northern station was 0.7 cm s⁻¹ to 240°T, and that at 6615 m depth at the southern station was 0.5 cm s⁻¹ to 267°T. A westward mean flow prevailed at the stations, and no cyclonic circulation with mean flows of the opposite directions was observed in the Mariana Trench at a longitude of 142°35′ E. Power spectra of daily mean currents showed three spectral peaks at periods of 100 days, 28–32 days and 14–15 days. The peak at 100 day period was common to the power spectra.     

Modification of the damping function in the k–ε model to analyse oscillatory boundary layers

A simple relationship has been developed between the wall coordinate y⁺ and Kolmogorov's length scale using direct numerical simulation (DNS) data for a steady boundary layer. This relationship is then utilized to modify two popular versions of low Reynolds number k–ε model. The modified models are used to analyse a transitional oscillatory boundary layer. A detailed comparison has been made by virtue of velocity profile, turbulent kinetic energy, Reynolds stress and wall shear stress with the available DNS data. It is observed that the low Reynolds number models used in the present study can predict the boundary layer properties in an excellent manner.     

Decomposition of Phytoplankton in Seawater. Part I: Kinetic Analysis of the Effect of Organic Matter Concentration

Decomposition experiments were conducted on cultured phytoplankton (Skeletonema costatum) in seawater containing decomposer and consumer of size less than 500 μm. We determined the decomposition rates of bulk particulate organic matter (POM), the ratio of labile to semi-refractory fractions in the POM, and the POM carbon/ nitrogen (C/N) ratio during decomposition. To identify the kinetic mechanisms involved in the reactions of different order (e.g., first- and second-order), we studied the sensitivity of reaction rates to the initial concentration of POM, ranging from 2.4 to 71 mg-C L⁻¹. The results showed that decomposition consists of two first-order reactions: decomposition of labile and of semi-refractory particulate organic carbon (POC). The decomposition rate constants found for labile (0.13 day⁻¹ at 20°C), and semi-refractory POC (0.008 day⁻¹ at 20°C), and the carbon weight ratio of semi-refractory POC (13% at 20°C), were insensitive to the initial organic matter concentration. The time-dependence of the C/N ratio was also independent of this initial concentration. The decomposition rate constants and the content of semi-refractory POC did not change, regardless of the absence or presence of 25–500 μm organisms in natural seawater. This revised version was published online in July 2006 with corrections to the Cover Date.