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1.
Shizuo Tsunogai 《Journal of Oceanography》1972,28(4):145-152
A simple advection-diffusion model is applied to the deep water of the North Pacific Ocean. The physical mixing parameter, i.e., the ratio of vertical advection velocity (W) to vertical eddy diffusivity (D), is obtained from the vertical distribution of a conservative property such as salinity. The rate of decomposition of organic matter is estimated from the oxygen consumption rate which is obtained from dissolved oxygen content. The calcium carbonate flux in the deep water is obtained from alkalinity. Using these values and the vertical distribution of a radioisotope,14C or226Ra, the vertical eddy diffusivity and the upwelling velocity are found to be 1.2 cm2/sec and 1.4 ×10–5 cm/sec, respectively, at the Geosecs 1969 station. The oxygen consumption rate at 3 km depth of the station is found to be 1.4×10–3ml/l/yr. 相似文献
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Methane in the East China Sea water 总被引:1,自引:0,他引:1
Methane in the East China Sea water was determined four times at a fixed vertical section along PN line consisting of 11–14 stations, in February 1993, October 1993, June 1994 and August 1994. The mean concentration of methane in the surface water was not significantly higher than that in the open ocean. The methane concentration below the pycnocline increased during the stratified period in summer to autumn and reached to 15 nmoles/l at most in October. The concentration of methane was fairly well correlated with AOU in the layer below the pycnocline in the stratified season. This means that methane in the bottom water has only a single source, which is expected to be anoxic sediments near the coast, and that the oxidation rate of methane in the water is extremely slow in the oxic water. The high methane observed in October completely disappeared in February, indicating that the methane was escaped to the atmosphere or transported to the pelagic ocean by the Kuroshio current. The East China Sea, therefore, is not a large direct and stationary source for the atmospheric methane, but may have some role as a source by supplying it sporadically to the atmosphere in early winter or indirectly from the surface of the pelagic ocean. 相似文献
5.
Shuichi Watanabe Naoto Higashitani Nobuo Tsurushima Shizuo Tsunogai 《Journal of Oceanography》1994,50(4):415-421
The concentration of methane in seawater was determined approximately once a month for one year from August 1990 to July 1991 at a station close to the center of Funka bay (92 m depth) and some supplementary observations were also carried out. The concentration of methane was usually increased with increasing depth, suggesting that methane was emitted from the bottom of the bay. While highly variable both spatially and temporally, the emission was intense in March and April, a period immediately after the spring bloom of phytoplankton. The maximum of methane found in the intermediate water suggests its source from the slope of the bay. The concentration of methane in the surface water changed seasonally and also interannually. The annually averaged flux of methane transferred to the atmosphere in the bay was estimated to be 6×10–3 gCH4m2/day. The coastal zone in the world may be a significant source of the atmospheric methane, although its source strength has yet to be accurately estimated from more data in different coastal seas. 相似文献
6.
The spring bloom of phytoplankton was studied in March in Funka Bay, Japan, to test the Tsunogai (1979)'s hypothesis regarding the role of silicate in the bloom. The hypothesis comprises two parts. 1) Diatoms are predominant when all the physical and chemical conditions are adequate for plankton growth. 2) Since the Si:P ratio of the diatom body is usually much larger than that of sea water, flagellates (non-siliceous phytoplankton) replace diatoms after dissolved silicate in the sea water has been almost completely consumed by diatoms. At the end of the bloom in late March phosphate still remained in the water but silicate was exhausted and the main species of phytoplankton changed from diatoms to flagellates. Grazing pressure by zooplankton at this time was not so great. A model using the data on assimilation rates of silicate showed a dramatic change of silicate uptake in late March. Poison in scallops caused byProtogonyaulux sp. (dinoflagellates) rapidly increased from mid-April at all stations along the coast of Funka Bay. All of these findings support Tsunogai's hypothesis. 相似文献
7.
Metal-organic complexes of transition elements removed by Amberlite XAD-2 resin from seawater pumped up from under the ground were determined. The proportions of iron, copper and zinc retained on the resin to dissolved forms of these metals were about 70, 40 and 5%, respectively, while manganese, cobalt and nickel were not retained on the resin. These results suggest that although iron may be retained in colloidal form, a significant fraction of copper is present in some organic form(s). 相似文献
8.
Sea water samples were collected from various depths in the North Pacific (40–21°N) along 165°E in 1991. Their total carbonate (total dissolved carbonate species) contents were determined with random errors less than 0.2% by a coulometric method. The preformed carbonate contents defined by Chen (1982) were calculated from the obtained data and other observed data including potential temperature, salinity, dissolved oxygen and total alkalinity. The same calculation was done for the GEOSECS data obtained in nearly the same region in 1973. The difference between the two data sets reveals that the preformed carbonate has increased by 180±41 gC/m2 during the last 18 years. This value is comparable or somewhat larger than 150 gC/m2 obtained in the case that the ocean uptakes 3 GtC/yr for 18 years and distributes it equally among the world oceans. Based on the results, a hypothesis on the missing sink for the anthropogenic carbon dioxide is presented, in that the missing sink is the intermediate waters formed in the northern North Pacific and the Southern Ocean besides the deep waters formed in the North Atlantic and the Southern Ocean. 相似文献
9.
Microbial manganese oxidation in seawater was carried out in enrichment cultures which were obtained from the seawater supply system at the Marine Science Museum, Tokai University (Shimizu-shi, Japan). The manganese oxide formed was well-crystallized todorokite. The major element composition was within the range of marine manganese concretions and the O/Mn molar ratio was 1.8. The conditions for formation of manganese oxide minerals in marine environments are discussed on the basis of these results. 相似文献
10.
A simple indirect method for the determination of organic carbon in marine particulate matter is proposed. The recommended procedure is as follows: The dried sample is ashed at 450°C for about 24 hr. The ashed sample is put into a Teflon vessel followed by a mixed solution of nitric acid, perchloric acid and hydrofluoric acid. The vessel is sealed and allowed to stand at 150°C for 5 hr. The concentrations of Si and Al in the digested solution are determined. The organic carbon content (Cal-C, %) is calculated by the following equation: Cal-C=0.52 ([CF]–0.10 [Opal]–0.03 [A-Si]), where [CF] is the combustible fraction (%), [Opal] is the biogenic-SiO2(%), and [A-Si] is the content of aluminosilicate mineral (%). 相似文献