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111.
The concentrations of DMS were simultaneously measured in both water and air at the sea surface on board a vessel during a trans-Pacific cruise around 40° N in August 1988. Those in the surface seawater varied widely with a mean of 162 ng S/1 and a standard deviation of 134 ng S/1 (n=37), but the variation was not a mere fluctuation and the high concentration (376 ng S/1) was found in the area between 145° W and 170° W. The atmospheric DMS concentration varied more widely with a mean value of 177 ng S/m3 and a standard deviation of 203 ng S/m3 (n=23). The diurnal variation of DMS was not significant in the air near the sea surface. However, the concentrations in the surface water was fairly well correlated with those in the surface air. The correlation coefficient (r 2=0.86) was larger than that between the atmospheric concentration and outflux of DMS (r 2=0.64). These findings mean that the turnover time of DMS in the atmosphere is not extremely short. Based on the linear relation between the atmospheric and seawater DMS, the turnover time of the atmospheric DMS has been calculated to be 0.9 days with an uncertainty of around 50%. The oxidation rate agrees fairly well with that expected from the OH radical concentration in the marine atmosphere.  相似文献   
112.
A sediment core covering the last 145 kyrs was collected in the western subarctic Pacific (WSAP), and analyzed for Ba, U, Al, Sc, La, Yb, Th, biogenic opal (Opal) and organic carbon (Corg) as well as its isotopic ratio (δ13C). This study examined the change of past biological production in WSAP with multiple proxies, together with understanding the relation between Loess from the Asian continent and the biological production. The Loess content was estimated from the metal components, Al, Sc, La, Yb and Th. In this high latitude core (50°N), the Loess content was generally high during the glacial periods, but it was also high even in some interglacial periods. The excess amount of Ba relative to the detrital material composition, Baex, showed the best correlation with the Vostok δD (r = 0.72, p < 0.001), indicating that the biological production was lower in the glacial periods than in the interglacials. This corroborates the pervasive correlation between Baex in the polar region, WSAP and the Antarctic Sea, and Antarctic temperature, combined with previous research. This correlation might be explained by the stratification caused by cooling. In addition, the time variations of Baex in WSAP were similar to those of Baex in the Okhotsk Sea and of other proxies (Corg and Opal) in both the Okhotsk and the Bering Sea, indicating the spatial homogeneity of Baex in WSAP including proximal marginal seas. The Opal content was more weakly correlated with the Vostok δD (r = 0.46, p < 0.001) than Baex, reflecting that Opal in WSAP including proximal marginal seas was spatially heterogeneous compared to Baex. While both the Corg content and Uex, the excess amount of U relative to the detritus composition, were not positively correlated with the Vostok δD, they behaved similarly in the sediments. The positive correlation between δ13C and the Vostok δD (r = 0.42, p < 0.001), between δ13C and Baex (r = 0.60, p < 0.001) and between δ13C and Opal (r = 0.36, p < 0.01) indicates that δ13C in WSAP may give some information on the phytoplankton growth rate. There was not a significant correlation between the spatially homogeneous Baex in WSAP and Loess (r = − 0.16, p > 0.01), suggesting that the increase of biological production with the increase of Loess supply during the glacial periods did not occur.  相似文献   
113.
The dissolved inorganic carbon (DIC) and related chemical species have been measured from 1992 to 2001 at Station KNOT (44°N, 155°E) in the western North Pacific subpolar region. DIC (1.3∼2.3 µ mol/kg/yr) and apparent oxygen utilization (AOU, 0.7∼1.8 µmol/kg/yr) have increased while total alkalinity remained constant in the intermediate water (26.9∼27.3σθ). The increases of DIC in the upper intermediate water (26.9∼27.1σθ) were higher than those in the lower one (27.2∼ 27.3σθ). The temporal change of DIC would be controlled by the increase of anthropogenic CO2, the decomposition of organic matter and the non-anthropogenic CO2 absorbed at the region of intermediate water formation. We estimated the increase of anthropogenic CO2 to be only 0.5∼0.7 µmol/kg/yr under equilibrium with the atmospheric CO2 content. The effect of decomposition was estimated to be 0.8 ± 0.7 µmol/kg/yr from AOU increase. The remainder of non-anthropogenic CO2 had increased by 0.6 ± 1.1 µmol/kg/yr. We suggest that the non-anthropogenic CO2 increase is controlled by the accumulation of CO2 liberated back to atmosphere at the region of intermediate water formation due to the decrease of difference between DIC in the winter mixed layer and DIC under equilibrium with the atmospheric CO2 content, and the reduction of diapycnal vertical water exchange between mixed layer and pycnocline waters. In future, more accurate and longer time series data will be required to confirm our results.  相似文献   
114.
Uranium in coastal sediments of Tokyo Bay and Funka Bay   总被引:2,自引:0,他引:2  
The sediment cores from Tokyo Bay and Funka Bay were analyzed for U and its isotopic ratio,234U/238U, after dissolving them in 0.1 M HCl, and 30% H2O2 in 0.05 M HCl. A small fraction of U in the anoxic sediments was dissolved in 0.1M HCl and even the added yield tracer,232U, was lost. The isotopic ratio of H2O2 soluble U in the sediments was equal to that of seawater, suggesting that the H2O2 soluble U in the sediments is authigenic. The 6M HCl solution dissolved part of the lithogenic U besides the authigenic U. The depth profiles of U from the two bays resembled each other. The authigenic U comprised more than half of the total U even at the surface and increased with depth down to 70 cm, showing small maxima at about 20 cm. The concentration of refractory U was nearly constant with depth and similar to that of the pelagic sediments. The highest U concentration, 6 µg g–1 which was about 5 times that of the pelagic sediments, was observed in the layer between 70 and 160 cm depth in Tokyo Bay. The annual sedimentation rates of U in the Tokyo Bay sediments were 2.6 tons at the surface and 7.0 tons at the 70–160 cm depth. The increase in U with depth should be due to the deposition of interstitial U either diffusing downward from the surface indicating the trapping of seawater U, or otherwise diffusing upward from the deeper layer indicating the internal cycling of U within the sediments.  相似文献   
115.
在湍流局地平衡假设下 ,建立了齐次湍能输运方程封闭模型 (HKE) ,并在平板边界层的两种经典流动中加以检验 ,给出 HKE封闭下的流速、湍流动能和湍流混合系数剖面的形式解。结果表明 ,HKE可以避免在流速剪切为零时的无湍流混合问题 ,其解与 L aufer湍流实验吻合 ,因而HKE模型比混合长理论有更合理的内涵。文中还给出 HKE封闭的浅海动力学模型 ,以湍应力和水位梯度力的平衡为运动的基本受力平衡 ,进行了模型的量阶分析和运动分析 :当阻尼频率和运动频率同量阶时 ,惯性运动不可忽略 ;在潮振荡占优的浅海中 ,对流非线性相对于惯性运动为小量 ;当阻尼频率足够大时 ,科氏力项相对于湍应力也可能为小量。  相似文献   
116.
A combined structure is assumed to be composed of a rigid part and a flexible part. Each component structure would have a different period of natural vibration if it were built independently. When they are combined in one structure and subjected to an earthquake, there must be generated some interaction forces so that the component structures will have a common vibration. In this paper is an analytical method described to evaluate such interaction forces The general principle is as follows. For each of the component structures, equations of motion taking account of the unknown interaction forces are derived first. Then by eliminating the interaction forces, equations of motion of the combined structure are obtained. After solving these equations and substituting the solution into the equations of motion of the component structures, the unknown interaction forces are obtained directly In the present paper, two structures corresponding to two-degree elastic systems are considered; numerical examples also are included.  相似文献   
117.
A series of measurements of ice-nucleating particles (INPs) were performed at two sites in Beijing. At the Beijing Meteorological Service (BMS) site, which was an urban site, no INPs were found to be active above–15°C. However, at the Yanjiaping (YJP) site, which was a rural site, the concentration of INPs active at temperatures above–15°C was found to be as high as 1.73 g–1. Two parameterizations were constructed by respectively fitting the data obtained at BMS site and YJP site. The two parameterizations, as well as another parameterization from the literature, were implemented into a parcel model to investigate the effect of INPs active above–15°C on phase partitioning in mixed-phase clouds. At a vertical velocity of 0.01 m s–1, which is typical for stratiform clouds associated with frontal systems, the INPs active above–15°C nucleate ice crystals at low levels. The growth of these ice crystals remarkably reduces both the maximum liquid water mixing ratio and the altitude where the maximum liquid water mixing ratio is reached. When the vertical velocity of the parcel is increased to 0.1 m s–1 or an even higher value, the evolution of liquid water mixing ratio is not controlled by the INPs active above–15°C but those active below–15°C.  相似文献   
118.
Chen  Yang  Cui  Yanxing  Sheng  Xiaoxuan  Jiang  Wensheng  Feng  Shizuo 《Ocean Dynamics》2020,70(6):759-770
Ocean Dynamics - The 3D Lagrangian residual velocity (LRV) is solved analytically in a narrow bay employing a vertically varying eddy viscosity coefficient. The nondimensional vertical profile of...  相似文献   
119.
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   
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