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31.
226Ra and Ba show a general linear correlation in the oceanic water column within the uncertainties of the data: the slope of the line is about 4.6 nanomoles (nmoles) Ra/mole Ba, the intercept being at about 4 nmoles Ba/kg. This demonstrates the usefulness of Ba as a “chemical analogue” of Ra. Box-model calculations indicate that the average deep-water excess of Ra over Ba should be about 10% relative to the surface. This is consistent with the observations outside the deep northeast Pacific. However, the uncertainties in the data are such that the regional variation in the primary input cannot be resolved. In the deep waters of the North Pacific there is in fact a large excess of Ra relative to Ba. The one detailed profile presently available (204) can be explained consistently by a simple vertical advection-diffusion model.  相似文献   
32.
Fluxes of metals to the top and bottom surfaces of a manganese nodule were determined by combining radiochemical (230Th,231Pa,232Th,238U,234U) and detailed chemical data. The top of the nodule had been growing in its collected orientation at 4.7 mm Myr?1 for at least 0.5 Myr and accreting Mn at 200 μg cm?2 kyr?1. The bottom of the nodule had been growing in its collected orientation at about 12 mm Myr?1 for at least 0.3 Myr and accreting Mn at about 700 μg cm?2 yr?1. Although the top of the nodule was enriched in iron relative to the bottom, the nodule had been accreting Fe 50% faster on the bottom.232Th was also accumulating more rapidly in the bottom despite a 20-fold enrichment of230Th on the top.The distribution of alpha-emitting nuclides calculated from detailed radiochemical measurements matched closely the pattern revealed by 109-day exposures of alpha-sensitive film to the nodule. However, the shape and slope of the total alpha profile with depth into the nodule was affected strongly by226Ra and222Rn migrations making the alpha-track technique alone an inadequate method of measuring nodule growth rates.Diffusion of radium in the nodule may have been affected by diagenetic reactions which produce barite, phillipsite and todorokite within 1 mm of the nodule surface; however, our sampling interval was too broad to document the effect. We have not been able to resolve the importance of nodule diagenesis on the gross chemistry of the nodule.  相似文献   
33.
We present the distribution of226Ra in eight vertical profiles from the eastern Pacific. The profiles are located along a meridional trend near 125°W, from 43°S to 29°N. Surface226Ra concentrations are about 7 dpm/100 kg, except for the two stations south of 30°S where the higher values are due to the Antarctic influence. Deep waters show a distinctive south-to-north increase in the226Ra content, from about 26 to 41 dpm/100 kg near the bottom. Unlike in the Atlantic and Antarctic Oceans, the effect of226Ra injection from bottom sediments is clearly discernible in the area. The presence of this primary226Ra can be traced up to at least 1–1.5 km above the ocean floor, making this part of the sea bed among the strongest source regions for the oceanic226Ra. Numerical solutions of a two-dimensional vertical advection-diffusion model applied to the deep (1.2–4 km)226Ra data give the following set of best fits: upwelling velocity(Vz) = 3.5m/yr, vertical eddy diffusivity(Kz) = 0.6cm2/s, horizontal (north-south) eddy diffusivity(Ky) = 1 × 107cm2/s, and water-column regeneration flux of226Ra(J) = 3.3 × 10?5dpmkg?1yr?1 as an upper limit. These parametric values are in general agreement with one-dimensional (vertical) model fits for the Ra-Ba system. However, consideration of226Ra balance leads us to suspect the appropriateness of describing the vertical exchange processes in the eastern Pacific with constantVz and Kz. If future modeling is attempted, it may be preferable to treat the area as a diffusion-dominant mixing regime with depth-dependent diffusivities.  相似文献   
34.
A fiber extraction technique is used to concentrate Ra and Th isotopes from 1000 liters or more of seawater. Natural226Ra and234Th are used as yield tracers. In the equatorial Pacific the228Ra activity of surface water varies from 20 to 1 dpm/1000 kg and generally decreases away from continental shelf areas. Across the Peru Current System, this decrease is modeled as one-dimensional diffusion and indicates the possibility of two flow regimes with distinct characteristic mixing lengths and apparent eddy diffusivities of 105 and 107 cm2/s. The perturbing effects of advection and equatorial upwelling west of the Galapagos Islands are noted. Off the coast of Southern California a vertical228Ra distribution gives an apparent diffusivity of 1.6 cm2/s for the upper thermocline.226Ra concentrations near the coast appear to be higher than the open ocean values at comparable depths, which may reflect supply of this isotope from continental shelf sediments and/or upwelling. The insoluble daughter/soluble parent activity ratios228Th/228Ra and234Th/238U in the equatorial Pacific surface water display latitudinal trends which may be correlated with productivity variations. Near the coast of California these ratios reflect the differing oceanographic conditions north and south of Pt. Conception indicating a mean chemical removal time constant on the order of 4 months for Th and other highly reactive elements within the Southern California Bight. The232Th content of seawater sampled is less than 0.1 μg/1000 1; most of the published values for seawater232Th could well be too high. A comparison of the two methods of determining228Ra (via228Ac and via228Th) made on 64 seawater samples shows that the time delay required by the228Th method is more than compensated by its better analytical simplicity and precision.  相似文献   
35.
A method is proposed by which the degree of attrition of the tests of certain foraminifera species, such as Globorotalia menardii and Globorotalia tumida, is used to “scale” the amount of CaCO3 that has been dissolved from sediment. The scale is calibrated experimentally in the laboratory. The method has been applied to three calcareous cores from the Pacific and the Indian Oceans. It is shown that the original CaCO3 contents in these cores were high (82–95%) and relatively uniform compared to the present down-core values. About 65 to 85% of the originally deposited CaCO3 has been dissolved, corresponding to dissolution rates on the order of 0.1-0.3 moles/cm2/yr. These results indicate that appreciable solution could have occurred on sea floor rich in calcareous sediments and that the variation in CaCO3 content in a core may have resulted largely from dissolution. The difference in the degree of solution between glacial and interglacial sediments in these cores is not so distinct, with ? 10% less intense dissolution during glacial times on the average. However, the dissolution minimum occurring around the late Wisconsin glaciation (10,000–20,000 yr B.P.) previously noted in several cores elsewhere is confirmed. At that time, near the site of core M70 PC-20 in the southwest Pacific, the CO32? concentration of the bottom water is estimated to have been approximately 5% higher than the present value, and the calcite lysocline was about 300 m deeper. To evaluate possible variations in CaCO3 deposition rate across the glacial-interglacial transitions requires precise age control, which the present study lacks.  相似文献   
36.
Water samples from both hot and artesian springs in Kuantzeling in west-central Taiwan have been collected on a regular basis from July 15, 1999 to the end of August 2001 to measure cation and anion concentrations as a tool to detect major earthquake precursors. The data identify chloride and sulfate ion anomalies few days prior to major quakes and lasting a few days afterward. These anomalies are characterized by increases in Cl- concentrations from 34.9% to 41.2% and 71.5% to 138.1% as well as increases in SO42- concentrations from 232.7% to 276.8% and 100.0% to 155.1% above the means in both hot and artesian springs. The occurrence of these anomalies is probably explained first as stress/strain-induced pressure changes in the subsurface water systems which then generate precursory limited geochemical discharges at the levels of subsurface reservoirs. Therefore, finally leading to the mixing of previously separated subsurface water bodies occurs. This suggests that the hot and artesian springs in the Kuantzeling area are possible ideal sites for recording strain changes serving well as earthquake precursors.  相似文献   
37.
We investigated whether the radiation pressure on dust grains alone may account for driving winds in semiregular, irregular and non-variable AGB stars. A simple theoretical model is employed to calculate the limits for the radiatively driven winds and to compare theoretical predictions with observations. Present analysis indicates, that for most of the objects in the studied sample of 67 oxygen-rich and 40 carbon-rich mass-losing AGB stars radiation pressure on dust grains alone is not effective enough to drive the observed circumstellar outflows.  相似文献   
38.
The distributions of cosmogenic nuclide10Be in the upper and lower salt units from a core (36.4°N, 94.5°E) in the Chaidamu Basin, Qinghai, China have been measured by means of accelerator-mass spectrometer. The comparison of these10Be results measured on salt and detritus fractions shows that the geochemical behaviour of10Be is detritus-phile. In this area10Be influx is different in the past tens of thousands of years, which is suggested to be related to climatic fluctuations during late Pleistocene. It seems that10Be influx is higher in the humid climate environnent than in the dry climate environment. The230Th-age estimates of two salt units have been determined. The corrected ages of the lower unit show a climate shift from humid to dry at about 50 Ka ago in this area.  相似文献   
39.
Attempts have been made to study the entire growth history of a manganese nodule from the northern part of Peru Basin in the Pacific using radiochemical profiles of 230Th232Th, 227Th230Th, and 10Be9Be. Combined with the observations on Fe-Mn contents and textural variation, the radiochemical data indicate that the nodule grew more or less concentrically throughout most of its existence since it formed 1.5 my ago, receiving Mn from both bottom water and pore water. This condition appeared to have changed about 180 ky ago when the growth became asymmetric in that the top and bottom sides became fixed in their relative positions on the sea floor. Since then, the bottom side accreted with a fast rate of close to 200 mm/my, apparently fueled by the supply of diagenetically remobilized Mn in pore water from the sediment substrate. In the meantime, the top side accumulated at about 6 mm/my, a value which is in the normal range for deep-sea nodules having their Mn supplied from the hydrogenous source.  相似文献   
40.
Beryllium isotopes (10Be and9Be) have been measured in suspended particles of < 1 mm size collected by mid-water sediment traps deployed in the eastern Pacific at MANOP sites H (6°32′N, 92°50′W, water depth 3600 m) and M (8°50′N, 104°00′W, 3100 m). For comparison, surface sediments from box cores taken from the two sites were also studied. The concentrations of10Be and9Be in sediment-trap particles are about an order of magnitude smaller than those in the bottom sediments which contain about 8 × 109 and 6 × 1016 atoms g−1 of10Be and9Be, respectively. The sediment trap samples collected from 50 m off the bottom showed significant (26–63%) contributions from resuspended bottom sediments. The10Be/9Be ratio in trap samples varies from 3 to 20 × 10−8. The variation may partly result from varied proportion of authigenic/detrital material. The fluxes of both isotopes exhibit a very strong seasonality. The fluxes of10Be into the traps at about 1500 m are estimated as 9 × 105 and 4 × 105 atoms cm−2 a−1 at sites H and M respectively. These values are to be compared with the fluxes into the sediments of 4–5 × 105 atoms cm−2 a−1 at both locations. Good correlations exist between10Be,9Be and27Al indicating that the primary carrier phase(s) for the beryllium isotopes in the water column may be aluminosilicates.  相似文献   
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