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1.
Concentrations of Se in the pore-water and in the solid phase, and the concentrations of other diagenetic constituents (Fe, Mn, phosphate, ammonium and I) in pore-water, were determined in a sediment core from a 350-m deep station in the lower St. Lawrence Estuary. The concentration of dissolved Se in pore-water was 2.1 nmol kg−1 at the surface of the core, increasing to a maximum of 7.6 nmol kg−1 at a depth of 12 cm, and thereafter decreasing gradually with depth. This profile is similar to the profiles of Fe and phosphate, whose concentration maxima occur around 10 cm. The concentration of total sedimentary Se remained almost constant with depth (≈ 0.75 mg kg−1); however, a significant enrichment of oxalate-leachable Se was observed in the top 2 cm. The sedimentary cycling of Se appears to be closely related to that of Fe: adsorption of Se onto Fe oxyhydroxide at or near the sediment-water interface, release of the adsorbed Se by the reduction of Fe oxyhydroxide, and removal by formation of ferroselite (FeSe2) at depth. The pore-water flux of Se was estimated by two different methods, firstly from the pore-water gradient, and secondly by applying a box model to the oxalate-leachable solid-phase Se data. The methods agree well both giving values for the flux of 0.11 nmol cm−2 year−1. This agreement suggests that the loss of labile Se in the sediment is balanced by the upward flux of dissolved Se. 相似文献
2.
Kazufumi Takayanagi George T. F. Wong Margaret J. Filardo 《Journal of Oceanography》1989,45(2):129-133
Nitrate reductase activity and the concentrations of selenite and selenate were monitored for six months at the mouth of Chesapeake Bay (USA). A positive correlation was found between nitrate reductase activity and the concentration of selenite, suggesting that selenite may be formed in coastal waters and nitrate reductase may be involved in the process. 相似文献
3.
Hideko Nomura 《Astrophysics and Space Science》2004,292(1-4):435-438
We have constructed self-consistent temperature and density profiles of irradiated active protoplanetary disks, using a two-dimensional radiative transfer calculation. By means of these profiles we have studied the stabilization of the convective instability by radiative heating and the magnetorotational instability (MRI) via ohmic dissipation, taking into account the effect of dust particle growth. Simple chemistry such as ionization by cosmic rays and recombination on dust grains are used to calculate the ionization degree of gas in the disks. Our results show that the dust growth stabilizes the convective instability due to the 2D effect of radiative transfer, while it enhances the MRI through the decrease in the recombination of ions on the dust grains. In addition, the influences of the dust settling toward the midplane of the disks on the instabilities are discussed. 相似文献
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5.
An extremely complex outburst, part of which showed unsually rapid intensity fluctuations of a few second interval, was observed on 1970 November 5 with the 160 MHz interferometer of the Nobeyama Solar Radio Station. The pulsating source, which was stable in position and strongly circularly polarized ( 60 %), had an extension as large as 17 (7.5 × 105 km) in the east-west direction. The structure of the source remained unchanged while the source darkened and brightened repeatedly. The change of the source brightness occurred in a time shorter than a second.Two alternative mechanisms responsible for the pulsating phenomenon are suggested; (1) gyroresonance absorption of continuum radiation by a fast particle beam injected in a quasi-periodic manner into a large region of weak magnetic field, or (2) magnetohydrodynamic oscillation of the continuum source itself, which is intrinsically much smaller than observed. It is observed as a large source as a consequence of scattering of the emitted radiation in a region situated above the source. 相似文献
6.
Hideko Takayanagi Yasufumi Iryu Tsutomu Yamada Motoyoshi Oda Kazuyuki Yamamoto Tokiyuki Sato Shun Chiyonobu Akira Nishimura Tsutomu Nakazawa Satoshi Shiokawa 《Island Arc》2007,16(3):394-419
Abstract The lithology of shallow-water carbonates collected from 19 sites on 16 seamounts in six areas of the northwestern Pacific Ocean using the Deep-sea Boring Machine System are described. The areas include the Amami Plateau, Daito Ridge, Oki-Daito Ridge, Urdaneta Plateau, Kyushu-Palau Ridge and Ogasawara Plateau. Chronological constraint is provided by calcareous nannofossil biostratigraphy, planktonic foraminiferal biostratigraphy, larger foraminiferal biostratigraphy and strontium (Sr) isotope stratigraphy. Large amounts of shallow-water carbonates accumulated on the seamounts during the Oligocene, a relatively cool period, whereas limited carbonate deposits formed during the Early Miocene, a relatively warm period. This might indicate that deposition of shallow-water carbonates on seamounts in the northwestern Pacific Ocean was not necessarily controlled by climatic conditions, but was related to volcanism and tectonics that served as foundations for reef/carbonate-platform formation. Remarkable differences in biotic composition exist between Cretaceous and Cenozoic shallow-water carbonates. Late Cretaceous shallow-water carbonates are distinguished by the occurrence of rudists, solenoporacean algae and microencrusters. Middle Eocene to Early Oligocene shallow-water carbonates are dominated by Halimeda or nummulitid and discocyclinid larger foraminifers. Scleractinian corals became common from the Oligocene onward. Nongeniculate coralline algae and larger foraminifers were common to abundant throughout the Eocene to the Pleistocene. The replacement of major carbonate producers in the shallow-water carbonate factory during post-Cretaceous time is in accordance with previous studies and is considered to reflect a shift in seawater chemistry. 相似文献
7.
The non-linear response history and failure mechanism of coupled wall systems under dynamic loads and static loads are investigated through an analytical model. The walls and coupling beams are replaced by flexural elements. Axial and shear stiffnesses are included for the wall members. The stiffness characteristics of each member are determined by inelastic properties. The suitable hysteresis loops to each constituent member are established to include the specific characteristics of coupled wall systems. The computed results are compared with results obtained from tests using model structures statically and dynamically tested on the Illinois Earthquake Simulator. 相似文献
8.
Hironobu Harada Tatsuki Tsujimori Keitaro Kunugiza Katsuyuki Yamashita Shogo Aoki Kazumasa Aoki Hideko Takayanagi Yasufumi Iryu 《Island Arc》2021,30(1):e12389
Marble has a great potential to understand a history of various geological events occurring during tectonic processes. In order to decode metamorphic–metasomatic records on C–O isotope compositions of marble at mid-crustal conditions, we conducted a C–O–Sr isotope study on upper amphibolite-facies marbles and a carbonate–silicate rock from the Hida Belt, which was once a part of the crustal basement of the East Asian continental margin. Carbon and oxygen isotope analyses of calcite from marbles (Kamioka area) and a carbonate–silicate rock (Wadagawa area) show a large variation of δ13C [VPDB] and δ18O [VSMOW] values (from −4.4 to +4.2 ‰ and +1.6 to +20.8 ‰, respectively). The low δ13C values of calcites from the carbonate–silicate rock (from −4.4 to −2.9 ‰) can be explained by decarbonation (CO2 releasing) reactions; carbon–oxygen isotope modeling suggests that a decrease of δ13C strongly depends on the amount of silicate reacting with carbonates. The occurrence of metamorphic clinopyroxene in marbles indicates that all samples have been affected by decarbonation reactions. All δ18O values of calcites are remarkably lower than the marine-carbonate values. The large δ18O variation can be explained by the isotope exchange via interactions between marble, external fluids, and/or silicates. Remarkably low δ18O values of marbles that are lower than mantle value (~+5 ‰) suggest the interaction with meteoric water at a later stage. Sr isotope ratios (87Sr/86Sr = 0.707255–0.708220) might be close to their protolith values. One zircon associated with wollastonite in a marble thin-section yields a U–Pb age of 222 ± 3 Ma, which represents the timing of the recrystallization of marble, triggered by H2O-rich fluid infiltration at a relatively high-temperature condition. Our isotope study implies that the upper amphibolite-facies condition, like the Hida Belt, might be appropriate to cause decarbonation reactions which can modify original isotope compositions of marble if carbonates react with silicates. 相似文献
9.
Volume transport of the Soya Warm Current revealed by bottom-mounted ADCP and ocean-radar measurement 总被引：2，自引：2，他引：0
Yasushi Fukamachi Iori Tanaka Kay I. Ohshima Naoto Ebuchi Genta Mizuta Hideo Yoshida Shiro Takayanagi Masaaki Wakatsuchi 《Journal of Oceanography》2008,64(3):385-392
The vertical structure of the Soya Warm Current (SWC) was observed by a bottom-mounted acoustic Doppler current profiler (ADCP)
in the region of the SWC axis near the Soya Strait during a 1-year period from May 2004. The ADCP data revealed a marked seasonal
variability in the vertical structure, with positive (negative) vertical shear in summer and fall (winter and spring). The
volume transport of the SWC is estimated on the basis of both the vertical structure observed by the ADCP and horizontal structure
observed by the ocean radars near the strait. The transport estimates have a minimum in winter and a maximum in fall, with
the yearly-averaged values in the range of 0.94–1.04 Sv (1 Sv = 106 m3 s−1). These lie within a reasonable range in comparison to those through other straits in the Japan Sea. 相似文献
10.
The vertical distributions of Se (IV), Se (VI) and dissolved organic Se have been determined in the oxic and non-sulfide-bearing anoxic zones of the Orca Basin. In the oxic waters, the concentration of Se (IV) increases with depth gradually from 0.25 nmole/kg at the surface to a maximum of 0.46 nmole/kg at 750 m and then decreases with depth to a relatively constant concentration of 0.39 nmole/ kg below 1,230 m. The concentration of Se (VI) is rather uniform in the top 250 m at about 0.24 nmole/ kg. Below 250 m it increases with depth to 0.50 nmole/kg at 1.230 m, and it stays relatively constant below this depth. The concentration of organic Se increases from 0.50 nmole/kg at the surface to 1.39 nmole/kg at 78 m. A pronounced broad maximum of organic Se exists between 78 and 250 m. The concentration decreases with depth below 250 m, dropping sharply between 250 and 380 m and more gradually at greater depths. It becomes undetectable at 1,230 m. Organic Se is the dominant species above 250 m. Se (IV) is the most abundant between 250 and 1,000 m while Se (VI) becomes the dominant species below 1,000 m. The distributions of these three species can be explained by the biological uptake of Se in the surface waters and the multi-step regeneration of Se from biogenic particles at greater depths. In suboxic waters at the oxic-anoxic interface, the concentration of Se (IV) increases while that of Se (VI) decreases reflecting a change in redox conditions in the environment. In the anoxic brine, the concentration of Se (IV) is around 0.25 nmole/kg while Se (VI) is undetectable. The concentration of organic Se increases sharply in the suboxic waters and reaches 2.6 nmole/kg in the anoxic brines probably as a result of the decomposition of organic matter and/or a diffusive flux from the underlying sediment. 相似文献