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1.
The diffusion in a shearing oscillatory flow from an instantaneous surface point source is considered. An analytical solution
is obtained by Fourier transform. The results show that, for three dimensional diffusion in an oscillatory flow with constant
shear, the distribution of the contaminant follows the multivariate Gaussian distribution rule. When the frequency is very
high, or the time very short, the shear does not influence the diffusion. For moderate values of time, there are fluctuations
with longitudinal variance. For large values of time the longitudinal variance increases as t, and the peak concentration
decreases as t−1.5, which are faster than those in a flow without shear, but much slower than those in a steady flow, where the longitudinal
variance increases as t3 and the peak concentration decreases as t−2.5. The contaminant patch is elongated in the longitudinal direction of the shear flow and moves back and forth with the water
motion.
Contribution No. 1306 from the Institute of Oceanology, Academia Sinica. Received July 12, 1985 相似文献
2.
3.
Roberto F. Viotti Rosario González-Riestra Takashi Iijima Stefano Bernabei Riccardo Claudi Jochen Greiner Michael Friedjung Vito Francesco Polcaro Corinne Rossi 《Astrophysics and Space Science》2005,296(1-4):435-439
We review the main characteristics of the symbiotic system AG Draconis, with special emphasis on its optical and X-ray variations.
We also discuss the X-ray to visual energy distribution during quiescence and outburst and describe our spectroscopic and
X-ray observations during the 2003 outburst.
Based on X-ray observations collected with the XMM–Newton Observatory, on INES data from the IUE satellite, and on optical
spectra collected with the Asiago–Cima Ekar, Bologna–Loiano and La Palma–Galileo Italian telescopes. 相似文献
4.
Ryuji Okazaki Tomoki Nakamura Nobuo Takaoka Keisuke Nagao 《Meteoritics & planetary science》2003,38(5):767-781
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. 相似文献
5.
Kyu Han Kim Keisuke Nagao Hirochika Sumino Tsuyoshi Tanaka Takamasa Hayashi Toshio Nakamura Jong Ik Lee 《Chemical Geology》2008,253(3-4):180-195
We report analyses of noble gases and Nd–Sr isotopes in mineral separates and whole rocks of late Pleistocene (< 0.2 Ma) monzonites from Ulleungdo, South Korea, a volcanic island within the back arc basin of the Japan island arc. A Rb–Sr mineral isochron age for the monzonites is 0.12 ± 0.01 Ma. K–Ar biotite ages from the same samples gave relatively concordant ages of 0.19 ± 0.01and 0.22 ± 0.01 Ma. 40Ar/39Ar yields a similar age of 0.29 ± 0.09 Ma. Geochemical characteristics of the felsic plutonic rocks, which are silica oversaturated alkali felsic rocks (av., 12.5 wt% in K2O + Na2O), are similar to those of 30 alkali volcanics from Ulleungdo in terms of concentrations of major, trace and REE elements. The initial Nd–Sr isotopic ratios of the monzonites (87Sr/86Sr = 0.70454–0.71264, 143Nd/144Nd = 0.512528–0.512577) are comparable with those of the alkali volcanics (87Sr/86Sr = 0.70466–0.70892, 143Nd/144Nd = 0.512521–0.512615) erupted in Stage 3 of Ulleungdo volcanism (0.24–0.47 Ma). The high initial 87Sr/86Sr values of the monzonites imply that seawater and crustally contaminated pre-existing trachytes may have been melted or assimilated during differentiation of the alkali basaltic magma.A mantle helium component (3He/4He ratio of up to 6.5 RA) associated with excess argon was found in the monzonites. Feldspar and biotite have preferentially lost helium during slow cooling at depth and/or during their transportation to the surface in a hot host magma. The source magma noble gas isotopic features are well preserved in fluid inclusions in hornblende, and indicate that the magma may be directly derived from subcontinental lithospheric mantle metasomatized by an ancient subduction process, or may have formed as a mixture of MORB-like mantle and crustal components. The radiometric ages, geochemical and Nd–Sr isotopic signatures of the Ulleungdo monzonites as well as the presence of mantle-derived helium and argon, suggests that these felsic plutonic rocks evolved from alkali basaltic magma that formed by partial melting of subcontinental lithospheric mantle beneath the back arc basin located along the active continental margin of the southeastern part of the Eurasian plate. 相似文献
6.
Yusuke Seto Naoya Sakamoto Takashi Kaito Hisayoshi Yurimoto 《Geochimica et cosmochimica acta》2008,72(11):2723-2734
We report the mineral compositions and micro-texture of the isotopically anomalous (δ17,18OSMOW ∼ +180‰) Fe-S-Ni-O material recently discovered in matrix of the primitive carbonaceous chondrite Acfer 094 [Sakamoto N., Seto Y., Itoh S., Kuramoto K., Fujino K., Nagashima K., Krot A. N. and Yurimoto H. (2007) Oxygen isotope evidence for remnants of the early solar system primordial water. Science317, 231-233]. Synchrotron radiation X-ray diffraction and transmission electron microscopy studies indicate that this material consists of the symplectitically intergrown magnetite (Fe3O4) and pentlandite (Fe5.7Ni3.3S8) with magnetite/pentlandite volume ratio of ∼2.3. Magnetite forms column-shaped grains (10-30 nm in diameter and 100-200 nm in length); pentlandite occurs as worm-shaped grains or aggregates of grains 100-300 nm in size between magnetite crystals. Although both the X-ray diffraction and electron energy loss spectra support identification of iron oxide as magnetite, the electron diffraction patterns show that magnetite has a weak 3-fold superstructure, possibly due to ordering of vacancies. We infer that the isotopically anomalous symplectite formed by sulfurization and oxidization of metal grains either in the solar nebula or on an icy planetesimal. The intersite cation distribution of pentlandite suggests that timescale of oxidation was no longer than 1000 years. 相似文献
7.
Decadal variability of subsurface temperature in the North Pacific has been investigated. Two dominant regions were found;
the central subarctic region (CSa) and the north-eastern subtropical region (NESt). In CSa, cooling (warming) of wintertime
subsurface temperature corresponds to the large (small) temperature gradient and southward (northward) shift of subsurface
temperature front, associated with the increase (decrease) of positive wind stress curl and the southward (northward) shift
of curl τ zero line with 2 years delay. It is suggested that the relocation of subtropical-subarctic boundary plays an important
role. In NESt, importance of heat flux through the sea surface and heat divergence in the Ekman layer is also discussed.
This revised version was published online in July 2006 with corrections to the Cover Date. 相似文献
8.
The presence of organic ligands (L) whose conditional stability constants (KML) are strong enough to allow them to form complexes with copper has been reported in oceanic waters. However, there is no general agreement on the distributional characteristics of such strong ligands in the water column. We present that these inconsistencies are derived from not only different analytical methods employed for their detection but also different oceanographic conditions. In particular, the nature and quantities of detectable natural ligands are affected by what kind of form the ligands are presentin situ in different marine environments, that is, chemical speciation of natural ligands (ligand speciation), which depends strongly on the variations in concentrations of coexisting trace metals. Using published data from observations in the laboratory and the field, we provide limits to the ranges of conditional stability constants of organic ligands for copper, zinc and cadmium that are detectable by the extensively used direct metal-titration method. For example, our model indicates that organic ligands for copper with log KCuL(Cu)>12.4 in surface water and with log KCuL(Cu)>9.9 in deep water might not have been detected because stronger ligands had formed complexes with ambient metalsin situ at a station in the North Pacific. The estimation suggests that there is a basinscale difference in speciation of natural organic ligands and, moreover, that this difference influences metal speciation. It is postulated that comparisons of the occurrence and levels of organic ligands might not be possible among spatially and temporally different observations without reconciliation of the effects of speciation of the ligands, even if an identical method is used in every case. 相似文献
9.
Time series of the vertical distribution of resuspended matter and bottom current were collected concurrently during summer at a few anchored stations in the Seto Inland Sea. The vertical distribution of resuspended matter was measured every hour for about one tidal cycle and the three components of current fluctuation were obtained at each sampling station. Current data at each sampling station show that the bottom is hydraulically smooth.Assuming that the averaged vertical distribution of resuspended matter for one tidal cycle shows a steady state distribution, the settling velocityWs of resuspended matter is estimated to be in the range of 1.2×10–2 to 5.7×10–2 cm sec–1 from analysis of the averaged distributions.The relation between the erosion rate and the bottom shear stress for this study area is investigated and is compared with that for other areas. The results show that the erosion of sediment in the Seto Inland Sea during summer occurs even due to the low bottom shear stress which is considered as almost smooth hydraulically. 相似文献
10.
Yutaka W. Watanabe Yoshiyuki Takahashi Takashi Kitao Koh Harada 《Journal of Oceanography》1996,52(3):301-312
Concentrations of total carbonate, alkalinity and dissolved oxygen were obtained near the 1973 GEOSECS stations in the North Pacific subpolar region north of 40°N along 175°E between 1993 and 1994. A difference of excess CO2 content between the GEOSECS and our expeditions was estimated. The maximum difference in water column inventory of excess CO2 has increased by about 280 gC m–2 above 2000 m depth which apparently means an uptake of excess CO2 taken from air to sea during the last two decades. An averaged value of the annual flux of excess CO2 at 75–1000 m depth was 8.63±2.01 gC m–2yr–1 in the North Pacific subpolar region. By introducing the annual flux of excess CO2 into a two-box model for the North Pacific subpolar region, a penetration factor of excess CO2 from air to sea was obtained to be 1.08×10–2 gC m–3ppm–1 in the North Pacific subpolar region. Based on this factor, the surface concentration of excess CO2 in the North Pacific subpolar region was estimated to be 68 mole I–1, suggesting that the North Pacific subpolar region absorbed atmospheric excess CO2 more than the saturated concentration of excess CO2. Total amount of excess CO2 taken from the North Pacific subpolar region by 1993 was estimated to be 36.2×1015 gC, which was equal to about one tenth of that released by human activities after the preindustrial era. 相似文献