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21.
海洋生态系统动力学浅说   总被引:4,自引:1,他引:4  
讨论了海洋生态系统动力学的研究目的,任务和特点。阐述了它的基本理论问题,此外,协同性,可预报性,突变性以及稳定性是人们关切的问题也是海洋生态系统动力学理论研究的重要内容。并对海洋生态系统动力学模型及模拟的基本概念和了描述,进而说明建模时要注意抽象与简化。最后就我国开展海洋生态系统动力学研究提出了一点看法。  相似文献   
22.
Major gases dissolved in seawater were accurately determined with a shipboard gas chromatographic method. The standard deviations were 0.28, 0.34 and 0.36% for N2, O2 and Ar, respectively. The method was applied to water from the northwestern North Pacific Ocean collected in May to June 2000. We got 127 duplicate seawater samples from the surface 200 m layer at 11 stations. The O2 concentrations obtained by this method agreed with those given by the Winkler method. All the seawater samples from the surface 200 m, especially those from the upper 30 m, were supersaturated with respect to atmospheric N2 and Ar concentrations. In the topmost 30 m layer, the degrees of supersaturation in the inventory were 2.7–4.3% for N2 (ΔN2) and 1.7–2.6% for Ar (ΔAr), and their ratios, ΔN2/ΔAr, ranged from 1.53 to 1.81. This supersaturation seems to be chiefly due to air bubbles injected into the water and dissolved due to the water pressure, because the N2/Ar ratio of the air is around 2. The amounts of air bubbles dissolved in the upper 30 m water were relatively large, with mean value of 0.41 ml/kg or 18.4 μmol/kg. The ΔN2, ΔAr and ΔN2/ΔAr values were all positively well correlated with the wind velocities averaged for the last 24 hours prior to sampling, allowing the conclusion to be drawn that the weaker the wind velocity, the dissolved gas composition approaches in equilibrium with the air; while the stronger the wind velocity, it approaches in the air composition. This revised version was published online in July 2006 with corrections to the Cover Date.  相似文献   
23.
It is suggested that the shallow sea circulation should be related to the Lagrangian residual circulation but not to the conventional Eulerjan mean circulation, and further, the first order Lagrangian residual circulation-the mass-transport velocity field is used to define the steady circulation as the lowest order shallow sea circulation.The set of equation governing the shallow sea circulation is reformulated, which shows that there are no the so-called “tidal surface source” and the “tidal stress”. A vorticity equation for the stream function of horizontal transports is derived, which is easily solved by the conventional numerical methods.An intertidal convection-diffusion equation governing the concentration of conservative and passive tracer is derived. Differing from the conventional equation, the equation derived in the present paper reveals the Lagrangian convection and has no need to introduce the artificial hypothesis for the so-called “tidal dispersion”.The theory presented here is base  相似文献   
24.
超浅海风暴潮模型提出后[2],对渤海风潮,作为超浅海问题,进行了数值研究[1]。其结果的分析和观测资料的比较都表明了该模型有一定的应用价值;故,对超浅海风暴潮模型作进一步的探讨是有一定意义的。尤其因为我国是一个多浅水域和多风暴潮的国家,这种研究就具有更重要的意义。  相似文献   
25.
26.
Settling particles were collected at 1,460 m and 3,760 m depth in the Antarctic Ocean with sediment traps of time series type. The total deployment period of 40 days was divided into four terms of 10 days each. Seawater samples were collected both at deployment and retrieval of the traps at each site. During the 42 days the concentration of silicate in the surface water decreased by 32%, whereas those of nitrate and phosphate decreased by only 4–5%. The total particulate flux in the Antarctic Ocean is the largest among those hitherto observed in the world ocean. The time variation of the particulate flux at 1,460 m depth almost coincided with that at 3,760 m. The settling particles were comprised roughly of 80% biogenic silica, 15% organic matter and 5% other substances including sea salt. The clay fraction was only 0.05% at 1,460 m depth. The settling flux of biogenic silica agrees fairly well with the calculated rate of change in the concentration of silicate in the surface 100 m. Thus it is concluded that preferential propagation of diatoms reduces the concentration of silicate prior to other nutrients in the Antarctic Ocean.  相似文献   
27.
Vertical profiles of210Pb and230Th in the deep water were analyzed by using a simple one-dimensional model. Both nuclides are considered to settle down with the velocity of 1×10–4 cm/sec. The diameter of particle corresponding to the velocity is calculated to be 5, while only about 10 % of the nuclides can be collected on filter paper with a pore size of 0.5. It is supposed that the nuclides exist in particulate materials which is changeable in size. This suggestion is supported from the following evidences. (1) The directly observed behavior of marine snow and the size distribution of particles observed with a coulter counter. (2) The existence of many chemical elements of which residence time is about 150 years. (3) Their possible existence as eutectic solid phases in the seawater. (4) The consistency of the observed accumulation rate of pelagic sediments with that estimated from the settling velocity. (5) The consistency of the decomposition rate of organic matter in the deep water estimated from the oxygen comsumption with that from the settling velocity.  相似文献   
28.
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   
29.
Since 1960 when I was a senior student, I have studied natural phenomena observed in the hydrosphere and atmosphere by means of chemical elements. Each of the phenomena is, in general, very complicated and so I have attempted to depict the whole picture of material circulation in the marine environment by studying its various aspects at the same time. My chief strategy has been to use natural radio-nuclides as clocks of various phenomena, and to use sediment traps for the determination of vertical fluxes in the ocean. The many results I have obtained can be summarized as follows. 1. I have found that several sporadic events control the material exchange through the atmosphere. These include the strong winter monsoon and typhoons that transport sea-salt particles to the Japanese Islands, theKosa episodes that transport soil dust to the ocean, and storms that result in exchange of sparingly soluble gases such as oxygen and carbon dioxide at the air-sea interface. I have also proved quantitatively that the source of aluminosilicate material in pelagic sediments is air-borne dust. 2. I have proposed a model,Settling model, for the removal of chemical substances from the ocean and found various lines of evidence supporting the model. This model predicts the reversibility in the existing state of insoluble chemical elements in seawater among large settling particles, small suspended particles and colloidal particles that pass through a membrane filter and explains well their behavior in the ocean. I have first precisely measured calcium and iodine in the ocean and have explained their distributions on the basis of the solution and redox equilibria. 3. Using chemical tracers, I have estimated the vertical eddy diffusion coefficients to be 1.2 cm2sec−1 for the Pacific deep water, 0.5 cm2sec−1 for the deep Bering Sea water and 3–80 cm2sec−1 for the Pacific surface water, and have studied the structure of water masses in the western North Pacific and the Sea of Japan. I have also invented and applied a method for the calculation of the age of deep waters using radiocarbon. 4. I have calculated the rates of decomposition of organic matter and the regeneration rates of chemical components in the deep and bottom waters as well as coastal waters by modelling water circulation and mixing. Particulate fluxes and regeneration rates are larger in the deep waters beneath the more biologically productive surface waters. I have stressed the role of silicate in the marine ecosystem, especially in the succession of phytoplankton species. 5. I have quantitatively studied the migration of chemical elements during the early diagenesis of bottom sediments especially manganese using chemical and radiochemical techniques. Manganese is being actively recycled not only in coastal seas but also in pelagic sediments except in the highly oligotrophic subtropical ocean. This recycling can explain the formation of manganese nodules and enables us to balance the manganese budget in the ocean.  相似文献   
30.
The distributions of CFC (chlorofluorocarbon) in the water column was determined twice in 2000 and 2001 in the northwestern Japan Sea. In 2000 the CFC-11 concentration decreased almost exponentially with depth from 6 pmol/kg at a few hundred m deep to 0.3 pmol/kg or less at the bottom of about 3400 m depth at three stations (40–41°N, 132–133°E) about 300 km off Vladivostok. In 2001 the CFC-11 concentration increased sharply up to 2 pmol/kg in the bottom water, while it did not increase at a station (42.0°N, 136.5°E) about 450 km away to the northeast. This is due to the renewal of the bottom water which is replaced by the surface water flowing down along the continental slope, as suggested by Tsunogai et al. (1999), who proposed the continental shelf pump. Furthermore, an increase in the CFC-11 concentration was observed throughout the entire water column above 3000 m depth, although the proportion of the increase was about 20%, which was one order of magnitude smaller than that in the bottom water. The increase in inventory is almost four times larger than that in the bottom water below 3000 m depth which is equivalent to about 1/6 of the total inventory found in 2000. The increase also means that 3% of the deep water was replaced by the recent surface water, or, if the turnover occurs every year, that the turnover time of the deep water to be about 30 years. This revised version was published online in July 2006 with corrections to the Cover Date.  相似文献   
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