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161.
A simplified technique for the rapid analysis of photosynthetic pigments in marine phytoplankton is described. The pigments extracted in N,N-dimethylformamide (DMF) are injected directly into the reverse-phase high-performance liquid chromatograph fitted with a photodiode array detector. We developed a new stepwise program; that is methanol-water (7525 v/v), methanol, methanol-acetone (8020) and methanol-acetone (6535). This program gives a good separation of at least 13 carotenoids, and 10 chlorophylls and their derivatives, completed within 20 min. The quantitative precision is high; the maximum standard error was less than 6%. The stability of pigments in DMF were also considered for application of this technique to the lab work on board the ship.  相似文献   
162.
Microbial degradation of five crude oils such as Arabian light, Berri, Murban, Khafji and Minas crude oil by a pure bacterial strain,Pseudomonas sp. isolated from the sea water sampled at Kawasaki Harbor in Tokyo Bay, was studied experimentally in the enriched seawater medium.The degradation of crude oils was determined in total residual oil and in four fractions of saturated, aromatics, asphaltene and column residue by use of the column chromatography with activated alumina.The saturated fraction was shown to be most biodegradable. The aromatics followed for all five crude oils examined and the asphaltene was biodegradable to some extent. The column residue was not apparently degraded byPseudomonas sp. within 30 days. Each of Arabian light, Berri or Murban crude oil was degraded from 59 to 63.5 %, Khafji crude oil 49 % and Minas crude oil, solid at room temperature, only 33 %. Degradation rate of the five crude oils was determined to be in a range from 2.88 to 17.3 mg-oil 1–1 hr–1 or from 6.0×10–12 to 1.56×10–10 mg-oil cell–1 hr–1. Relative degradation ofn-paraffins of different carbon numbers in the saturated fraction was found to be similar regardless of carbon number for the five crude oils.  相似文献   
163.
As part of the research program WEST-COSMIC Phase I (1997–2001), vertical profiles down to the greater depths (0–2000 m or 5800 m) of the plankton community structure composed of heterotrophic bacteria, phytoplankton, protozooplankton and metazooplankton were studied at one station in each subarctic (44°N) and in transitional region (39°N), and two stations in subtropical region (30°N and 25°N); all in 137–155°E in the western North Pacific Ocean. The biomass of all four taxonomic groups decreased rapidly with increasing depths at all stations, although the magnitude of depth-related decrease differed among the groups. As plankton community structure, metazooplankton biomass and bacterial biomass occupied >50% of the total in 0–2000 and 2000–4000 or 5000 m strata, respectively, at subarctic and transitional stations, while bacterial biomass contributed to >50% of the total consistently from 0 through 4800 or 5800 m at subtropical stations. Metazooplankton biomass integrated over the greater depths exhibited a clear latitudinal pattern (high north and low south), but this was not the case for those of the other taxonomic groups. As a component of metazooplankton, an appreciable contribution of diapausing copepods to the metazooplankton was noted at subarctic and transitional stations, but they were few or nil at subtropical stations. As protozooplankton assemblages, heterotrophic microflagellates (HMF) and dinoflagellates were two major components at subarctic and transitional stations, but were only HMF predominated at subtropical stations. From biomass ratios between heterotrophic bacteria, HMF and dinoflagellates, “sinking POC-DOC-heterotrophic bacteria-HMF-heterotrophic dinoflagellates” link was proposed as a microbial food chain operative in the deep layer of the western North Pacific. All results are discussed in the light of latitudinal differences in the structure and functioning of plankton community contributing to the ‘biological pump’ in the western North Pacific Ocean. This revised version was published online in July 2006 with corrections to the Cover Date.  相似文献   
164.
The first CO2 exposure experiments on several species of pelagic copepods inhabiting surface and deep layers in the western North Pacific were conducted. Living organisms were collected from two layers between the surface and 1,500 m between latitudes of 11 and 44°N, and they were exposed aboard ship to various pCO2 up to about 98,000 μatm. Mortality of copepods from both shallow and deep layers in subarctic to subtropical regions increased with increasing pCO2 and exposure time. Deep-living copepods showed higher tolerance to pCO2 than shallow-living copepods. Furthermore, deep-living copepods from subarctic and transitional regions had higher tolerances than the subtropical copepods. The higher tolerances of the deep-living copepods from subarctic and transitional regions may be due to the adaptation to the natural pCO2 conditions in the subarctic ocean.  相似文献   
165.
Ocean-bottom pressure records obtained near the epicenter of the 2011 Tohoku-Oki earthquake were examined to test whether the earthquake was preceded by substantial precursory crustal deformation. The seafloor data enabled us to search for small-scale preslip near the epicenter that would be difficult to identify from terrestrial geodetic data. After treating the data to reduce nontectonic fluctuations, we obtained a time series of seafloor vertical deformation in the epicentral region with a noise level of 2–4 cm. No significant crustal deformation related to preslip was detected in the period of roughly a day before the mainshock, whereas postseismic deformation associated with the largest foreshock 2 days before the mainshock was apparent. From our quantitative estimate of the sensitivity of the seafloor network in detecting slip on the plate interface, we conclude that the Tohoku-Oki earthquake was not preceded by preslip with moment release greater than moment magnitude (Mw) 6.2 in the vicinity of the hypocenter or greater than Mw 6.0 along the subduction interface near the trench.  相似文献   
166.
A geochemical method for estimation of the maximum temperature of mudstones is proposed. The extents of epimerization of the sterane and the hopane are used. The temperature function is:
Tmax. (°C) = 606015.0?In(dUdUdV)?273
where U = ln (1 ? α/0.54), V = ln(1 ? β/0.61), α = 20S-/20S- + 20R-24-ethyl-5α(H), 14α(H), 17α(H)-cholestane(C29-sterane) and β = 22S-/22S- + 22R-17α(H), 21β(H)-bishomohopane(C32-hopane). The value of dU/dV can be obtained from the tangent to the evolution curve in the UversusV. This temperature function is applicable to the temperature analysis in the range of 50°C–150°C.  相似文献   
167.
A new synchrotron X-ray diffraction study of chromium oxide Cr2O3 (eskolaite) with the corundum-type structure has been carried out in a Kawai-type multi-anvil apparatus to pressure of 15 GPa and temperatures of 1873 K. Fitting the Birch–Murnaghan equation of state (EoS) with the present data up to 15 GPa yielded: bulk modulus (K 0,T0), 206 ± 4 GPa; its pressure derivative K0,T , 4.4 ± 0.8; (?K 0,T /?T) = ?0.037 ± 0.006 GPa K?1; a = 2.98 ± 0.14 × 10?5 K?1 and b = 0.47 ± 0.28 × 10?8 K?2, where α 0,T  = a + bT is the volumetric thermal expansion coefficient. The thermal expansion of Cr2O3 was additionally measured at the high-temperature powder diffraction experiment at ambient pressure and α 0,T0 was determined to be 2.95 × 10?5 K?1. The results indicate that coefficient of the thermal expansion calculated from the EoS appeared to be high-precision because it is consistent with the data obtained at 1 atm. However, our results contradict α 0 value suggested by Rigby et al. (Brit Ceram Trans J 45:137–148, 1946) widely used in many physical and geological databases. Fitting the Mie–Grüneisen–Debye EoS with the present ambient and high-pressure data yielded the following parameters: K 0,T0 = 205 ± 3 GPa, K0,T  = 4.0, Grüneisen parameter (γ 0) = 1.42 ± 0.80, q = 1.82 ± 0.56. The thermoelastic parameters indicate that Cr2O3 undergoes near isotropic compression at room and high temperatures up to 15 GPa. Cr2O3 is shown to be stable in this pressure range and adopts the corundum-type structure. Using obtained thermoelastic parameters, we calculated the reaction boundary of knorringite formation from enstatite and eskolaite. The Clapeyron slope (with \({\text{d}}P/{\text{d}}T = - 0.014\) GPa/K) was found to be consistent with experimental data.  相似文献   
168.
The historical trend of pollution sources of Pb in Tokyo Bay, Japan was investigated on the basis of Pb isotope ratios in a sediment core. The isotope ratios of anthropogenic Pb decreased gradually with increasing Pb concentration in the 1900s–1970s, suggesting a combination of Pb sources with various isotope ratios. In contrast, the isotope ratios of anthropogenic Pb in the 1980s–2000s showed no significant trend, and corresponded to the Pb isotope ratios in the three principal rivers flowing into the bay. It is probable that river bottom sediments contaminated with Pb are principal sources of anthropogenic Pb in Tokyo Bay.  相似文献   
169.
The compositional dependence on the density of liquid Fe alloys under high pressure is important for estimating the amount of light elements in the Earth’s outer core. Here, we report on the density of liquid Fe–Si at 4 GPa and 1,923 K measured using the sink–float method and our investigation on the effect of the Si content on the density of the liquid. Our experiments show that the density of liquid Fe–Si decreases from 7.43 to 2.71 g/cm3 non-linearly with increasing Si content (0–100 at%). The molar volume of liquid Fe–Si calculated from the measured density gradually decreases in the compositional range 0–50 at% Si, and increases in the range 50–100 at% Si. It should be noted that the estimated molar volume of the alloys shows a negative volume of mixing between Fe and Si. This behaviour is similar to Fe–S liquid (Nishida et al. in Phys Chem Miner 35:417–423, 2008). However, the excess molar volume of mixing for the liquid Fe–Si is smaller than that of liquid Fe–S. The light element contents in the outer core estimated previously may be an underestimation if we take into account the possible negative value of the excess mixing volume of iron–light element alloys in the outer core.  相似文献   
170.
In aquatic environments extracellular enzymes are bound to microbial cells or exist in a free and adsorbed state. Various filters have been used to fractionate these enzymatic activities, but enzymes may be readily adsorbed onto some materials, and such adsorption can induce errors in the estimation of enzymatic activity. In this study we examined three filters to determine the most suitable filter for fractionation when estimating proteolytic enzyme activity in seawater. We found that the polycarbonate Nuclepore membrane, widely used for size fractionation because of its pore-size accuracy, was the most favorable for this purpose, even though it adsorbed slightly more enzymes than the low-protein-binding polyethersulfone membrane. We also found that trypsin-and chymotrypsin-type enzymes were more easily adsorbed than aminopeptidases.  相似文献   
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