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401.
Radio observations from decimetric to submillimetric wavelengths are now a basic tool for the investigation of comets. Spectroscopic observations allow us: (i) to monitor the gas production rate of the comets, by directly observing the water molecule, or by observing secondary products (e.g., the OH radical) or minor species (e.g., HCN); (ii) to investigate the chemical composition of comets; (iii) to probe the physical conditions of cometary atmospheres: kinetic temperature and expansion velocity. Continuum observations probe large-size dust particles and (for the largest objects) cometary nuclei.Comets are classified from their orbital characteristics into two separate classes: (i) nearly isotropic, mainly long-period comets and (ii) ecliptic, short-period comets, the so-called Jupiter-family comets (JFCs). These two classes apparently come from two different reservoirs, respectively, the Oort cloud and the trans-Neptunian scattered disc. Due to their different history and—possibly—their different origin, they may have different chemical and physical properties that are worth being investigated.The present article reviews the contribution of radio observations to our knowledge of the JFCs. The difficulty of such a study is the commonly low gas and dust productions of these comets. Long-period, nearly isotropic comets from the Oort cloud are better known from Earth-based observations. On the other hand, JFCs are more easily accessed by space missions. However, unique opportunities to observe JFCs are offered when these objects come by chance close to the Earth (like 73P/Schwassmann-Wachmann 3 in 2006), or when they exhibit unexpected outbursts (as did 17P/Holmes in 2007).About a dozen JFCs were successfully observed by radio techniques up to now. Four to ten molecules were detected in five of them. No obvious evidence for different properties between JFCs and other families of comets is found, as far as radio observations are concerned.  相似文献   
402.
Two different simulation experiments of prebiotic synthesis were carried out in a CH4/N2/H2 atmosphere with spark discharge activation of aqueous aerosols and liquid water. In both cases, a hydrophilic tholin and a hydrophobic tholin were obtained. The methodology developed by our group for the characterisation of hydrophilic tholins [Ruiz-Bermejo, M., Menor-Salván, C., Mateo-Martí, E., Osuna-Esteban, S., Martín-Gago, J.A., Veintemillas-Verdaguer, S., 2008. Icarus 198, 232-241] was used in order to study the hydrophobic tholins. The gas precursors of the tholins from mixtures containing CH4, with and without H2, were studied. We propose that the formation of the hydrophobic tholins involves the formation of unsaturated oligomeric hydrocarbon chains from vinyl and acetylene monomers, as well as allene derivatives formed in the gas phase after the incorporation of polar groups into these hydrocarbon chains. Finally, we compare our results concerning hydrophobic tholins with HCN polymers, since it is generally suggested that the polymeric material formed in spark experiments are possible oligomers of HCN, and that Titan’s tholins could be poly-HCN.  相似文献   
403.
This paper describes a proposed high resolution soft X-ray and Extreme Ultraviolet spectroscopy mission to carry out a survey of Stellar and Galactic Environments (SAGE). The payload is based on novel diffraction grating technology which has already been proven in a sub-orbital space mission and which is ready to fly on a satellite platform with minimal development. We discuss the goals of a SAGE base-line mission and demonstrate the scientific importance of high resolution spectroscopy in the Extreme Ultraviolet for the study of stars and the local interstellar medium.  相似文献   
404.
对磷矿石中P2O5、Al2O3,caO、MgO、Fe2O3、Cd测定方法进行研究,确定试验最佳条件。元素回收率95.3%~105.4%,相对标准偏差(n=12)为2.53%-5.80%,检出限为0.5×10^-6-7.86×10^-6。经几种国家标准物质及矿石样品分析验证,结果满意。  相似文献   
405.
A suite of sulfate minerals were characterized spectrally, compositionally, and structurally in order to develop spectral reflectance-compositional-structural relations for this group of minerals. Sulfates exhibit diverse spectral properties, and absorption-band assignments have been developed for the 0.3-26 μm range. Sulfate absorption features can be related to the presence of transition elements, OH, H2O, and SO4 groups. The number, wavelength position, and intensity of these bands are a function of both composition and structure. Cation substitutions can affect the wavelength positions of all major absorption bands. Hydroxo-bridged Fe3+ results in absorption bands in the 0.43, 0.5, and 0.9 μm regions, while the presence of Fe2+ results in absorption features in the 0.9-1.2 μm interval. Fundamental SO bending and stretching vibration absorption bands occur in the 8-10, 13-18, and 19-24 μm regions (1000-1250, 550-770, and 420-530 cm−1). The most intense combinations and overtones of these fundamentals are found in the 4-5 μm (2000-2500 cm−1) region. Absorption features seen in the 1.7-1.85 μm interval are attributable to HOH/OH bending and translation/rotation combinations, while bands in the 2.1-2.7 μm regions can be attributed to H2O- and OH-combinations as well as overtones of SO bending fundamentals. OH- and H2O-bearing sulfate spectra are fundamentally different from each other at wavelengths below ∼6 μm. Changes in H2O/OH content can shift SO band positions due to change in bond lengths and structural rearrangement. Differences in absorption band wavelength positions enable discrimination of all the sulfate minerals used in this study in a number of wavelength intervals. Of the major absorption band regions, the 4-5 μm region seems best for identifying and discriminating sulfates in the presence of other major rock-forming minerals.  相似文献   
406.
High-resolution spectra of Venus and Mars at the NO fundamental band at 5.3 μm with resolving power ν/δν=76,000 were acquired using the TEXES spectrograph at NASA IRTF on Mauna Kea, Hawaii. The observed spectrum of Venus covered three NO lines of the P-branch. One of the lines is strongly contaminated, and the other two lines reveal NO in the lower atmosphere at a detection level of 9 sigma. A simple photochemical model for NO and N at 50-112 km was coupled with a radiative transfer code to simulate the observed equivalent widths of the NO and some CO2 lines. The derived NO mixing ratio is 5.5±1.5 ppb below 60 km and its flux is . Predissociation of NO at the (0-0) 191 nm and (1-0) 183 nm bands of the δ-system and the reaction with N are the only important loss processes for NO in the lower atmosphere of Venus. The photochemical impact of the measured NO abundance is significant and should be taken into account in photochemical modeling of the Venus atmosphere. Lightning is the only known source of NO in the lower atmosphere of Venus, and the detection of NO is a convincing and independent proof of lightning on Venus. The required flux of NO is corrected for the production of NO and N by the cosmic ray ionization and corresponds to the lightning energy deposition of . For a flash energy on Venus similar to that on the Earth (∼109 J), the global flashing rate is ∼90 s−1 and ∼6 km−2 y−1 which is in reasonable agreement with the existing optical observations. The observed spectrum of Mars covered three NO lines of the R-branch. Two of these lines are contaminated by CO2 lines, and the line at 1900.076 cm−1 is clean and shows some excess over the continuum. Some photochemical reactions may result in a significant excitation of NO (v=1) in the lowest 20 km on Mars. However, quenching of NO (v=1) by CO2 is very effective below 40 km. Excitation of NO (v=1) in the collisions with atomic oxygen is weak because of the low temperature in the martian atmosphere, and we do not see any explanation of a possible emission of NO at 5.3 μm. Therefore the data are treated as the lack of absorption with a 2 sigma upper limit of 1.7 ppb to the NO abundance in the lower atmosphere of Mars. This limit is above the predictions of photochemical models by a factor of 3.  相似文献   
407.
408.
Plant toxic biochemicals play an important role in defense against natural enemies and often are toxic to humans and livestock. Hyperspectral reflectance is an established method for primary chemical detection and could be further used to determine plant toxicity in the field. In order to make a first step for pyrrolizidine alkaloids detection (toxic defense compound against mammals and many insects) we studied how such spectral data can estimate plant defense chemistry under controlled conditions.In a greenhouse, we grew three related plant species that defend against generalist herbivores through pyrrolizidine alkaloids: Jacobaea vulgaris, Jacobaea erucifolia and Senecio inaequidens, and analyzed the relation between spectral measurements and chemical concentrations using multivariate statistics.Nutrient addition enhanced tertiary-amine pyrrolizidine alkaloids contents of J. vulgaris and J. erucifolia and decreased N-oxide contents in S. inaequidens and J. vulgaris. Pyrrolizidine alkaloids could be predicted with a moderate accuracy. Pyrrolizidine alkaloid forms tertiary-amines and epoxides were predicted with 63% and 56% of the variation explained, respectively. The most relevant spectral regions selected for prediction were associated with electron transitions and CH, OH, and NH bonds in the 1530 and 2100 nm regions.Given the relatively low concentration in pyrrolizidine alkaloids concentration (in the order of mg g−1) and resultant predictions, it is promising that pyrrolizidine alkaloids interact with incident light. Further studies should be considered to determine if such a non-destructive method may predict changes in PA concentration in relation to plant natural enemies. Spectroscopy may be used to study plant defenses in intact plant tissues, and may provide managers of toxic plants, food industry and multitrophic-interaction researchers with faster and larger monitoring possibilities.  相似文献   
409.
Leif Holmlid 《Icarus》2006,180(2):555-564
The long-lived excited state of matter called Rydberg Matter (RM) may explain several spectroscopic features in space, like the diffuse interstellar bands (DIBs) and the unidentified infrared bands (UIR, UIB). RM is here used to interpret some previously unexplained or inconsistent features in comets: (1) line absorption in the emission from the nucleus, (2) IR band emission from the coma, (3) selective and variable molecular line emission from the coma, (4) extended sources of molecules in the coma, (5) degree of linear polarization of light scattered from the coma. (1) The unexplained IR absorptions observed in the flyby of the nucleus of the Comet Borrelly agree well with RM emission bands observed by stimulated emission in the laboratory. It is proposed that RM is the so-called ultrared matter or at least formed from it. (2) The IR bands previously attributed to silicate particles are shown to be better described by RM theory. Transitions in atoms in RM are shown to dominate. (3) The inverted RM medium will optically amplify light from molecular transitions in the comet comae, in agreement with observations that many of the molecular IR emission lines lie within the emission bands from RM, or much too close to Rydberg transitions to be accidental. (4) The unexplained extended sources observed, e.g., for CO are proposed to be due to release of molecules previously incorporated in the RM clusters at low temperature. Such clusters may be the very small particles observed by space probes. (5) Finally, the largely unexplained measurements of the degree of linear polarization of scattered sunlight from comets are explained as due to scattering by the planar RM clusters. Quantitative agreement is demonstrated.  相似文献   
410.
R. Brunetto  F. Romano  S. Fonti  V. Orofino 《Icarus》2006,180(2):546-554
Laser irradiation experiments have been performed on powdered silicates (othopyroxene, clinopyroxene, and olivine) using a nanosecond pulse UV excimer laser (193 and 248 nm) to simulate the effects of space weathering induced on minor bodies of the Solar System by micrometeorite bombardment. We have used different fluences (from 0.05 to 2 J/cm2) to weather the samples, experimenting below and above the ablation threshold. All the irradiated materials have shown reddening and darkening of their UV-vis-NIR reflectance spectra. In addition we have found that: (1) below ablation threshold, weathering effects increase with increasing number of laser pulses, and with increasing fluence, confirming that a thermal process is active; (2) above ablation threshold, weathering is much stronger and efficient than in the previous case, and is independent on the number of pulses. We show that astrophysical time-scales, i.e. times necessary to obtain similar effects on planetary objects, are of about 108 yr for both olivine and pyroxene in the case of ablation. The time grows up to 1010 yr in the case of thermal effects. We infer that micrometeorite bombardment can be rightly simulated by laser irradiation only considering congruent laser ablation.  相似文献   
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