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11.
Crude petroleum was emulsified or degraded by marine microorganisms and physically altered by an artificial weathering process. Only the water-soluble fraction from emulsified crude petroleum inhibited glutamate uptake by marine microorganisms from South Carolina and Georgia coastal waters. Chloroform extraction recovered almost equal amounts of total hydrocarbon from each water-soluble fraction. Chromatographic data indicated that the composition of microbially emulsified petroleum was similar to that of microbially degraded petroleum. Emulsification of crude petroleum was only observed in summer water samples and did not consistently occur at a given location. Results of this study indicate that the process by which crude petroleum is altered will influence its toxicity to microbial heterotrophic activity.  相似文献   
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The sea surface is an important habitat for the developmental stages (eggs and larvae) of many fish and invertebrates; it is also a concentration point for anthropogenic contaminants entering the sea. Studies were conducted to determine the extent to which the sea surface of Puget Sound was toxic to the early life history stages of fish. Three urban bays with suspected contamination, a rural reference bay, and a Central Sound site were compared. Surface-dwelling eggs and organisms (zooneuston) were collected with a surface-skimming neuston net and their densities enumerated. Sand sole (Psettichthys melanostictus) embryos were exposed in the field and laboratory to the sea-surface microlayer. To develop a useful year-round approach to monitoring sea-surface toxicity, larval development of anchovies, kelp bass, and sea urchins was also evaluated as an indication of sea-surface microlayer toxicity.During the spawning season (February and March), urban boys in Puget Sound had lower concentrations of sand sole eggs and neustonic organisms on the sea surface than did the rural bayor Central Sound reference sites. Compared to the reference sites, laboratory exposure to surface microlayer samples collected from urban bay sites generally resulted in more chromsomal aberrations in developing sole embryos, reduced hatching success of sole larvae, and reduced growth in trout cell cultures. In situ hatching success of sole eggs was reduced by half or more in urban bays compared to reference sites.Toxicity was associated with visible surface slicks and, in urban bays, increased with increasing surface pressure (dynes cm−1). Results to be reported separately (Part II) indicate that toxicity is strongly correlated with the presence of high concentrations of polycyclic aromatic hydrocarbons and metals in the sea-surface microlayer. The toxicity of SMIC samples was similar when evaluated by sole, anchovy, kelp bass, or sea urchin tests. A sea-surface monitoring program could use sea urchin embryos to evaluate site-specific sea-surface toxicity throughout the year.  相似文献   
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Laboratory exposures of the urchin Lytechinus pictus to sediment dosed with varying concentrations of hydrogen sulfide (H2S), but without elevated organic material, were conducted. Changes in mortality, behavior, growth and gonad production were measured during 49 days' flow through exposures. Hydrogen sulfide concentrations of 165·8 μ liter−1 in pore water caused significant changes in all parameters measured. Concentrations as low as 32·9 μ liter−1 caused significant decreases in wet weight and male gonad production. A concentration of 91·8 μ liter−1 caused the mortality rate to increase 100-fold over control exposures (0·63 μ liter−1). Sublethal effects on growth and gonad production could have been caused by either direct biochemical inhibition by H2S or secondarily through behavioral modifications. Hydrogen sulfide concentrations above 165·8 μ liter−1 are common near sewage outfalls and could contribute to changes in species composition and sediment toxicity that occur there.  相似文献   
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The validity of analyses of elements in the femto- and picomolar ranges in waters and sediments can be assessed on the basis of several criteria: an evaluation of the chemical technique; the use of primary standards and intercalibration exercises; and chemical and geochemical coherence of the results. Herein are reported analyses of ruthenium, platinum, palladium, rhenium, iridium and gold in oceanic samples. The gold concentrations in surface seawaters, at least 25 times less than those previously reported, are in accord with the concentrations of their periodic table neighbors as well as with crustal and sedimentary contents. The remarkable concentration of rhenium in seawater, in relation to its very low crustal abundance, can be explained by the inertness of the perrhenate ion.  相似文献   
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Three data sets of suspensate concentrations, collected under different sampling plans, were analyzed to develop a minimal sampling period, consistent with a predetermined precision. Individual samples collected during any part of a given day were within ±50% of the daily average. In the main channel of the estuary, a monthly sampling scheme closely approximated a weekly pattern; however, seasonal sampling was unsatisfactory. Outside the main channel, weekly, monthly, and seasonal sampling patterns did not differ greatly. Variability in suspensate concentrations must be considered when calculating sediment flux in estuarine and coastal waters.  相似文献   
18.
Thermodynamic stability constants have been estimated for the complexation of iron(III) with catecholate-type siderophores isolated from the marine bacterium Alteromonas luteoviolacea and from the marine cyanobacterium Synechococcus sp. PCC 7002. Stability constants were determined utilizing the “chelate scale” of Taylor et al. (1994). The scale is based upon a linear relationship between the reduction potentials and the pH-independent thermodynamic stability constants for known iron(III) complexes. Log K values for the alterobactin B ferric iron complex are 43.6 ± 1.5 at pH 8.2 and 37.6 ± 1.2 at pH 6, consistent with a shift from bis-catecholate to monosalicylate/monocatecholate iron coordination with decreasing pH. Synechococcus isolates PCC 7002 Nos. 1 and 3 formed iron(III) complexes with stability constants of approximately 38.1 ± 1.2 and 42.3 ± 1.5, respectively. The binding strengths of the iron(III) complexes examined in this study are quite high, suggesting that catecholate siderophores may play a role in the solubilization and biological uptake of iron in the marine environment.  相似文献   
19.
Most coastal and ocean engineering laboratories employ techniques that use two or three spatially separated wave gages to estimate reflection of irregular waves in two-dimensional wave flumes. This paper presents a frequency domain method for separating incident and reflected wave spectra from co-located gages (gages located on the same vertical line). The technique is based on linear wave theory, and it can be applied to time series of sea surface elevation and horizontal water velocity collected in a vertical array, or it can be used with horizontal and vertical water velocity time series collected at the same point in the water column. Application of the method is limited to those frequencies showing good coherence between time series signals. Outside the range of good coherence, gross inaccuracies occur.The utility of the co-located gage method is illustrated using water velocity data collected in a wave flume with a laser Doppler velocimeter, and the method is validated for the case of complete reflection by a vertical wall. Side-by-side comparison to the spatially-separated wave gage method of Goda and Suzuki (1976) exhibited close agreement for a variety of irregular wave trains being weakly reflected by a mild sloping beach. The co-located gage method is useful in situations where there are spatial variations in the wavelength, such as on a mildly sloping bottom, or in the region close to highly reflective structures where errors arising from spatial variations in characteristic wave parameters would corrupt estimates made using the spatially-separated wave gage method.  相似文献   
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