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1.
The vertical distribution of salts brought by the Bosphorus undercurrent is numerically evaluated. By multiplying the average vertical salinity gradient by the diffusion coefficient,K
z
, and the cross-section of the sea at the appropriate depth, we can determine the total vertical salt flux,Q(z). The derivative ofQ with respect toz depicts the salt source intensity distribution over depth. The highest intensity, Q/z, matches the 200 m depth level, i.e. the shelf edge. Below 1500 m, Q/z equals merely 0.1% of the value observed at a depth of 200 m. Above 37 m, salts are noted to sink, which corresponds to their outflow with the Bosphorus current. The distribution of Q/z and the respective values of mineral phosphorus and hydrogen sulphide are matched up.Translated by Vladimir A. Puchkin. 相似文献
2.
Calcium-alkalinity relationship in the North Pacific 总被引：3，自引：0，他引：3
The dissolution of calcium carbonate in deep ocean water causes variation in calcium concentration (Ca) and alkalinity (TA) in the ratio of one to two. The decomposition of organic matter generates nitric acid, phosphoric acid and sulfuric acid. A proton flux which is derived from this process also changes alkalinity. Using the variation in nitrate concentration (NO3) as an index of the proton flux, the relationship betweenCa,TA andNO3 is expressed asCa=0.5TA+0.63NO3 The values of Ca obtained from direct measurements in the North Pacific are in good agreement with the values estimated from this equation. 相似文献
3.
Using climatological atlas data and historical hydrographic data, the relationship between dynamic height anomaly D and acoustic round-trip travel time in the Pacific Ocean is investigated. A tight, linear relation is found in a region centered on the Kuroshio and Kuroshio Extension. In this region, the slopem of the relation is approximately –50 dyn m s–1, about equal to the value expected for first-baroclinicmode response and twice as large as the value form in the Gulf Stream region of the Atlantic Ocean. The value ofm in the Pacific generally increases in magnitude towards the south and with increasing depth to which the integrals for D and are carried. It is changed only slightly by correcting for the temperature and salinity march of the seasons in the surface layer. The Kuroshio region is established as one in which the record of from an inverted echo sounder can be interpreted reliably in terms of D. An inverted echo sounder can also be used in this way in a number of other regions of the Pacific, although the available hydrographic data sets are too sparse to establish their boundaries clearly. 相似文献
4.
Shizuo Tsunogai Shuichi Watanabe Makio Honda Takafumi Aramaki 《Journal of Oceanography》1995,51(5):519-536
The importance of the North Pacific Intermediate Water as a sink for the anthropogenic carbon dioxide has been examined by mapping chemical and radiochemical properties at two isopycnal surfaces of of 26.6 ad 27.2 obtained in 1970's. Its radiocarbon contents in 1980's were determined for comparison. The isopleths of depth and salinity at the two isopycnal surfaces obviously show that the intermediate layer of the entire mid-latitudes of the North Pacific is occupied by a similar water mass. The distributions of dissolved oxygen contents and Si/N ratios in the intermediate water indicate its source in the northwestern North Pacific and its sink in the eastern Pacific. The 14C values clearly designate the intrusion of the artificial radiocarbon of mostly 1960's origin into the upper intermediate water of the western North Pacific having its maximum in the subarctic zone of 40–45°N and 160–180°E in 1973. The maximum region for tritium is much broader extending to the north. These suggest that the subboreal region is active in the gas exchange and/or the warm water residing for a long time at the surface and flowing into the region across the subarctic front sinks quickly in winter. At the lower isopycnal surface, the increase 14C value for 14±4 years was around 27, which is smaller than that expected from the total carbonate increase, indicating an active isopycnal mixing. 相似文献
5.
Regeneration of silicate in the Japan Sea, an example of semi-closed sea, was studied. In the Japan Sea Proper Water the apparent regenerative ratio of the nutrients was determined to be:O C N P Si=–289 (116)14.3181.It was assumed that the dissolved silicate present in sea water is grouped into three fractions; 1)preformed silicate of conservative nature, 2)oxidative silicate which dissolves in oxidation process of organisms with consumption of oxygen, and 3)non-oxidative silicate which dissolves without oxygen consumption. The dissolution rate ofnon-oxidative silicate in the Japan Sea Proper Water was estimated to be 0.07g-at. Si/l/yr from the data ofAOU values and assumed rates of oxygen consumption. This dissolution rate ofnon-oxidative silicate agreed with that obtained in the deep Pacific by the vertical advection diffusion model byKido andNishimura (1972). 相似文献
6.
The chemical states of iron in near-shore and deep-sea sediments were investigated by means of57Fe Mössbauer spectroscopy in combination with selective and nonselective chemical leachings. As far as a limited number of the sediments analyzed are concerned, Mössbauer spectra of near-shore sediments consist of high-spin paramgnetic ferrous (=1.13 mm/s, Eq=2.65 mm/s) and paramagnetic ferric (=0.35 mm/s, Eq=0.64 mm/s) components, while those of deep-sea sediments are composed of high-spin paramagnetic ferrous, paramagnetic ferrous, paramagnetic ferric and magnetic ferric (0.4 mm/s,H510 KG) components. The Fe2+/Fe3+ ratios of deepsea sediments are much smaller than those in near-shore sediments, while the total contents of iron in the former are much higher than those in the latter. This is principally due to the high contents of authigenic ferric oxides in deep-sea sediments. Further, in the aluminosilicate fraction, the Fe2+/Fe3+ ratios of deep-sea sediments are also smaller than those of near-shore sediments. This is probably attributed to high contents of clay minerals and authigenic aluminosilicates in deep-sea sediments relative to near-shore ones. The magnetic components in deepsea sediments are attributable to hematite, magnetite and/or maghemite. 相似文献
7.
PCBs, DDT compounds and HCH isomers were detected in the air and surface waters of the North Pacific and Indian Oceans, including the Bering Sea, East China Sea, South China Sea, Bay of Bengal and the Arabian Sea. The general concentrations of each chlorinated hydrocarbon were as follows: water PCBs 0.1 to 1.0, DDT 0.01 to 1.0, HCH 1.0 to 10 ngl
–1; air DDT 0.01 to 1.0, HCH 0.1 to 10 ng m–3. PCB concentrations in surface waters were slightly lower than those of the North Atlantic and North Sea previously reported, while DDT concentrations in the air and water were higher. Remarkably high concentrations of DDT and HCH were found in the air off the western coast of India. Also in the Pacific site off Central America, a fairly high concentration of DDT was observed in an air sample. These data suggest that large amounts of DDT and HCH are being used in the tropical zone, especially in southern Asia. Furthermore, high concentrations were observed both in the air and water of the Northwest Pacific between 30°N and 40°N latitude. There is a possibility that both pesticides are not only still being used in lower latitude countries but also in the mid-latitude ones of the Asian continent excluding Japan. In addition to this atmospheric circulation may also contribute to the concentration of these pesticides in the mid-latitudinal zone. 相似文献
8.
Radiocarbon and total carbonate data were obtained near the 1973 GEOSECS stations in the North Pacific along 30°N and along 175°E between 1993 and 1994. In these stations, we estimated radiocarbon originating from atomic bomb tests using tritium, trichlorofluoromethane and silicate contents. The average penetration depth of bomb radiocarbon during the two decades has deepened from 900 m to 1300 m. Bomb radiocarbon inventories above the average value for the whole North Pacific were found widely in the western subtropical region around 30°N both in the 1970s and 1990s, and its area in the 1990s was broader than that in the 1970s. In most of the North Pacific, while the bomb radiocarbon has decreased above 25.4, the bomb radiocarbon flux below 25.4 was over 1 × 1012 atom m-2yr-1 in the subtropical region around 30°N. In the tropical area south of 20°N, the bomb radiocarbon inventory below 25.4 increased from zero to over 10 × 1012 atom m-2 during the last three decades. These distributions suggest that the bomb radiocarbon removed from the surface is currently accumulated with bomb 14C flux of over 1 × 1012 atom m-2yr-1 below 25.4 in the subtropical region, mainly by advection from the higher latitude, and that part of the accumulated bomb 14C gradually spread southward with about 30 years. 相似文献
9.
The Algal Growth Potential (AGP) of water samples collected off Gamagori in Mikawa Bay was measured from May 1978 through February 1979, and the limiting nutrient was determined using regression analysis and enrichment bioassays. The surface and bottom water samples had AGP that produced increments of chemical oxygen demand (COD) of 2.1 mg l–1 and 3.1 mg l–1, respectively, on average. These values ofCOD correspond to 46% and 97% of the average COD values of the raw water samples at the surface and bottom, respectively. Seasonal changes of AGP showed a close correlation with those of dissolved inorganic nitrogen (DIN) concentration. Enrichment bioassays showed that DIN was the most deficient nutrient. The DIN:phosphate-phosphorus (PO4
3–-P) ratios and DIN: dissolved phosphorus (DP) ratios in the water samples were below the cellular N:P ratios of the natural algal populations. These results suggest that AGP was mainly limited by DIN concentration. 相似文献
10.
The selectivity of amino acid assimilation by marine bacteria was examined using seven kinds of14C-amino acids and the acid hydrolysate of14C-labelled proteins. It was found that the net assimilation and respiration by marine bacteria followed MICHAELIS-MENTEN kinetics for all of amino acids used in our experiments. Maximum velocities of amino acids were 0.01 to 0.19g carbon/hour per 2×107 cells for net assimilation and less than 0.18g carbon/hour per 2×107 cells for respiration at 20C. The velocity of gross assimilation was found with the following order: phenylalanine>valine, glutamic acid>serine, arginine>tryptophan>glycine. The assimilation velocities of amino acids in these laboratory works showed almost the same order as those in field experiments. The assimilation velocity of an amino acid was influenced by coexisting another amino acids or glucose. The assimilation velocity in lower substrate range of amino acids was directly proportional to the number of bacterial cells in the range from 6×102 to 3×104 cells per ml. No linear relation between the assimilation velocity of amino acids and reciprocal of absolute temperature was found, but a marked bending was observed at 15 to 20C. The velocity at the optimum temperature was three to six times of that at 5C. 相似文献
11.
The present study deals with the elucidation of sterol composition of the marine sediments in Kagoshima Bay. The identification of each sterol was performed by gas-liquid chromatography, Ag+ impregnated column chromatography, mass spectrometry, and nuclear magnetic resonance spectrometry. The sediment obtained near the estuary of River Koutsuki contained large portions of 5-stanols such as coprostanol and 24-ethylcoprostanol basides 5-stanols such as cholestanol, 24-methylcholestanol, and 24-ethylcholestanol in the sterol fraction. These 5-stanols in the marine sediment may be derived from the fecal contamination by domestic sewages. 相似文献
12.
Organic geochemical study of bulk organic matter (OM), hopanoid hydrocarbon and normal hydrocarbon (C23C35) was conducted for a 936-cm-long sediment core sample from the Oki Ridge of the Japan Sea (Core KH-79-3, C-3; 37°03.5 N, 134°42.6E, water depth 935 m). Stable carbon isotopic ratios were also measured for both bulk OM and individual hydrocarbons. The following results were obtained: (1) The weight ratios of total organic carbon to total nitrogen range from 6.2 to 9.4 in the core. The 13C values of bulk OM range from –25.1–20.7%.. The 13C values of OM in the sections of 140190 cm are lower (–25–24) than those in the other sections (–23–21). This result indicates that OM in the core except for the 140190 cm sections is essentially of marine origin. (2) The 13C value of diploptene (a hopanoid hydrocarbon) in the last glacial maximum (LGM), is –66.3 (vs. PDB), which indicates it originating in methanotrophic bacteria. This result provides evidence to support for the previous ideas (Oba et al., 1980, 1984; Masuzawa and Kitano, 1984) that the bottom waters in the Japan Sea were anoxic in LGM. (3) Long chain (C23C35) n-alkanes of higher-plant wax origin were found throughout the core. Their concentration is high in 140190 cm in depth, suggesting that eolian dust load was high in LGM. (4) The n-alkane/TOC ratio increases with decreasing 13C values of bulk OM. This result indicates that the load of terrestrial (probably eolian dust-derived) OM to the Japan Sea became higher in colder climates. (5) The CPI values of long-chain n-alkanes are different in different 13O stages of paleoclimate, probably reflecting variations in species of terrestrial higher plants as a result of climatological adaptations. 相似文献
13.
The stability constants for sulfate, chloride and hydroxide ions with cerium (III) in the solution at ionic strength of 0.67 have been determined by cation exchange method, the values of
1 and
2 for sulfate complexes of cerium being 40±13 and 453±140, respectively and those for chloride complexes being 1.28±0.23 and 0.56±0.076, respectively. The values of
1,
2 and
3 for hydroxide complexes of cerium were (4.5±0.9)×107, (3.3±0.7)×1014 and (1.8±0.7)×1023, respectively.Using the above constants the ratios of individual chemical species of144Ce were calculated in a solution at ionic strength of 0.67 containing sulfate and chloride ions approximately the same as in seawater of 35 %. The result of calculation indicates that the dominant species of144Ce in this solution is Ce(OH)3
0 at pH 8. 相似文献
14.
Shiro Gohda 《Journal of Oceanography》1974,30(4):163-167
The content and the oxidation state of arsenic and antimony in coastal seawater were determined coupled with chemical separation and neutron activation method. The contents of arsenic and antimony in coastal seawater were estimated to be 1.56–2.73g As/l, 0.25–0.57g Sb/l. Most parts of these elements exist as soluble ionic species, passing through 0.45 pore-size membrane filter, and at surface, 80–97% of arsenic occurs as arsenate and 70–94 % of antimony may occurs as antimonate. The vertical distribution of arsenite and arsenate is almost constant from the surface to 1,200 m depth. However the distribution of Sb(III) and Sb(V) is much more complicated with depth. 相似文献
15.
Chlorofluorocarbons (CFC-11 and CFC-12) in the intermediate water having between 26.4 and 27.2 were determined at 75 stations in the western North Pacific north of 20°N and west of 175.5°E in 1993. The intermediate water of 26.4–26.6 was almost saturated with respect to the present atmospheric CFC-11 in the zone between 35 and 45°N around the subarctic front. Furthermore, the ratios of CFC-11/CFC-12 of the water were also of those formed after 1975. These suggest that the upper intermediate water (26.4–26.6) was recently formed by cooling and sinking of the surface water not by mixing with old waters. The water below the isopycnal surface of 26.8 contained less CFCs and the area containing higher CFCs around the subarctic front was greatly reduced. However, the CFC age of the lower intermediate water (26.8–27.2) in the zone around the subarctic front was not old, suggesting that the water was formed by diapycnal mixing of the water ventilated with the atmosphere with old waters not containing appreciable CFCs, probably the Pacific Deep Water. The southward spreading rate decreased with depth and it was one sixth of its eastward spreading rate of the North Pacific Intermediate Water (NPIW). 相似文献
16.
The physico-chemical states of artificial radionuclides,90Sr,137Cs and144Ce in seawater were investigated by radiochemical analysis of filtered and unfiltered seawater. The difference of radionuclide concentrations between unfiltered and filtered seawaters was defined as the particulate form radioisotope and its particle ratio was discussed.Practically no particulate90Sr, greater than 0.22 in size, was observed in both coastal and open seawaters, but some of137Cs seemed to be insoluble in some circumstances, especially in coastal waters. A considerable amount of144Ce was found to be particulate.An estimation of the radionuclides in particulate form was made for Kashima-nada seawaters collected in 1970 to 1972, and it was shown that the possible occurrence of particulate radionuclides, greater than 0.22 in size, were 1% or less for90Sr and 6% for137Cs. In the coastal water, 80 % of144Ce were seemed to be in particulate form, but in the open seawater only a few%. The influences of suspended materials to137Cs and144Ce concentration levels in seawater were not negligible and further investigations are desirable. 相似文献
17.
Masao Minagawa Mami Ohashi Toshikatsu Kuramoto Norihiro Noda 《Journal of Oceanography》2001,57(3):285-300
Nitrogen isotope compositions of particulate organic matter and nitrate were analyzed for seawater sampled at five stations at the Alaskan Gyre, Western Subarctic Gyre and East China Sea, focusing on the samples from the surface to 5000 m water to characterize the nitrogen cycling in the subarctic North Pacific Ocean and its marginal sea. The 15N of particulate organic matter showed little agreement with a conceptual closed model that interprets isotopic variation as being caused by isotope discrimination on nitrate utilization. The 15N and 13C of particulate organic matter varied with the water depth. A correlation between isotope compositions and C/N elemental ratio was found generally at all stations, although some irregular data were also found in deep layers. We developed a hypothetical nitrogen balance model based on N2 fixation and denitrification in seawater and attempted to apply it to distinguish nutrient cycling using both 15N-NO3
– and N* variation in seawater. This model was applied to the observed data set of 15N-NO3
– and N* in the North Pacific water and estimated the 15N-NO3
– of primordial nitrate in the North Pacific deep water as 4.8. The North Pacific intermediate water for all stations showed similar 15N-NO3
– and N* values of 6 and –3 µmol/kg, respectively, suggesting a similar nitrogen biogeochemistry. In the East China Sea, analysis showed evidence of water exchange with the North Pacific intermediate water but a significant influence of nitrogen from the river runoff was found in depths shallower than 400 m. 相似文献
18.
Hirotaka Otobe 《Journal of Oceanography》1989,45(2):134-153
The downward short- and long-wave radiation fluxes at the sea surface (S, L) were measured aboard the R/VHakuho Maru, University of Tokyo, for the period of 117 days on six cruises from 1981 to 1985 in the western North Pacific near Japan. The upward fluxes of short- and long-wave radiation (S, L) were calculated by Payne's (1972) table and the Stefan-Boltzmann's law, respectively. The sensible and laten heat fluxes (Q
h
,Q
e
) were also estimated from an aerodynamic bulk method.From April to August, the daily mean value ofS varied with the amplitude of 100200 Wm–2. The value ofS was estimated approximately 6% ofS in all seasons. The difference betweenL andL was so small that the net radiation flux (Q
n
) was dominated byS. In addition, the net heat flux at the sea surface was also dominated byS due to small values ofQ
h
andQ
e
, and then the ocean was warmed at the rate of 111 Wm–2 in April and 63 Wm–2 in August in the Oyashio Area, and 132 Wm–2 in May and 164 Wm–2 in June in the Kuroshio Area, respectively.From September to March, a remarkable negative correlation between the day to day variation ofS and that ofL was observed except when an intense cold air outbreak occurred. It was found that the correlation was caused by the cloud climatological feature of the western North Pacific in this period.S was not a dominant factor in the net heat flux. The value ofQ
h
+Q
e
in the Kuroshio Area ranged from 260 Wm–2 to 630 Wm–2, much larger thanQ
n
which ranged from –8 Wm–2 to 92 Wm–2 in the leg mean values (each leg period was about 10 days). Then the ocean was cooled at the rate of –160–620 Wm–2 during this period. The net heat flux in the Kuroshio Area averaged over five legs from late November to February was –473 Wm–2. This value is 50100% larger than the climatological values reported so far.The temporal and spatial variability of radiation fluxes and heat fluxes during each leg was also discussed. 相似文献
19.
Jae Min Hyun 《Journal of Oceanography》1976,32(1):11-20
An analytical study is made of linearized internal wave dispersion relation in a density-stratified deep ocean with aN(z) profile which contains turning points. Principal emphasis is placed on obtaining the-k relationship for all frequencies. Taking advantage of the largeness of the nondimensional wavenumber (kS1), the mathematical tool to attack the governing Sturm-Liouville equation is a combination of the two-variable expansion (valid far away from the turning point) and the limit-process expansion (valid in the neighborhood of the turning point). The matching conditions for these two expansion schemes provide the desired-k relationship. A numerical example of this method demonstrates satisfactory agreement with the results obtained by the strict analytical solution and the multi-layered matrix numerical model. 相似文献
20.
Microbial mats were collected from a variety of sites near hydrocarbon vents along the slope in the northern Gulf of Mexico and, for comparison, from Warm Mineral Springs, Florida, USA. A predominant microorganism in each of the mats was the giant bacterium,Beggiatoa. Diameters of the bacterial filaments ranged from about 6 µm to approximately 200 µm. The latter organisms are the largest prokaryotic organisms yet found. All filaments over about 10 µm in diameter contained a large central vacuole, producing a cell with the cytoplasm as a cylindrical tube underlying the cytoplasmic membrane. Sulfur globules were confined to this peripheral layer. Push cores often contained pyrite tubules whose appearance is suggestive of aBeggiatoa origin. Determinations of
13C inBeggiatoa mats from vents along the Louisiana slope yielded values in the range of –26.6 to –27.9 (PDB), suggesting an unusually high degree of isotope fractionation (–24.9) relative to the carbon source in the ambient seawater, which is typical of sulfur-oxidizing chemoautotrophs. The presence of SO (elemental sulfur) within cells ofBeggiatoa resulting from oxidation of H2S supports the importance of bacterial sulfate reduction processes in the underlying vents for the sustenance of theBeggiatoa mats. 相似文献