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21.
George D. Nicolson 《Astrophysics and Space Science》1995,230(1-2):315-327
The development of radio astronomy at the Hartebeesthoek Radio Astronomy Observatory in South Africa is described. The Hartebeesthoek site was established originally by NASA as one of three Deep Space Stations equipped with 26-m parabolic reflector antennas. It was first used for radio astronomy by South Africa in terms of the NASA host nation agreement which allowed for its use at times when the facility was not needed for its primary purpose of tracking space probes. After NASA withdrew from South Africa in 1975, the South African Council for Scientific and Industrial Research took over the site and the 26-m parabolic reflector antenna, which NASA had abandoned in position, and established it as a national observatory. The development of the facility to the stage where it could support a variety of observing programmes such as continuum observations and mapping, spectroscopy and pulsar timing is described as well as the role played by the Observatory in global programmes of very long baseline interferometry. 相似文献
22.
R. Mewe 《Astronomy and Astrophysics Review》1991,3(2):127-168
Summary From the early discovery in 1948 of X-rays from the Solar corona, X-ray spectroscopy has proven to be an invaluable tool in studying hot astrophysical and laboratory plasmas. Because the emission line spectra and continua from optically thin plasmas are fairly well known, high-resolution X-ray spectroscopy has its most obvious application in the measurement of optically thin sources such as the coronae of stars. In particular X-ray observations with theEINSTEIN observatory have demonstrated that soft X-ray emitting coronae are a common feature among stars on the cool side of the Hertzsprung-Russell diagram, with the probable exception of single very cool giant and supergiant stars and A-type dwarfs. Observations with the spectrometers aboardEINSTEIN andEXOSAT have shown that data of even modest spectral resolution (/ = 10–100) permit the identification of coronal material at different temperatures whose existence may relate to a range of possible magnetic loop structures in the hot outer atmospheres of these stars. The higher spectral resolution of the next generation of spectrometers aboard NASA'sAXAF and ESA'sXMM will allow to fully resolve the coronal temperature structure and to enable velocity diagnostics and the determination of coronal densities, from which the loop geometry (i.e. surface filling factors and loop lengths) can be derived. In this paper various diagnostic techniques are reviewed and the spectral results fromEINSTEIN andEXOSAT are discussed. A number of spectral simulations forAXAF andXMM, especially high-resolution iron K-shell, L-shell, and2s-2p spectra in the wavelength regions around 1.9 Å, 10 Å, and 100 Å, respectively, are shown to demonstrate the capabilities for temperature, density, and velocity diagnostics. Finally, iron K-shell spectra are simulated for various types of detectors such as microcalorimeter, Nb-junction, and CCD. 相似文献
23.
Geraldo Magela da Costa Gabriel de Oliveira Polli Márcio A. Kahwage Eddy de Grave Antônio Claret Soares Sabioni Júlio Cesar Mendes 《Physics and Chemistry of Minerals》2006,33(3):161-166
Mössbauer spectra (MS) of blue, green and yellow beryl (ideally Be3Al2Si6O18) containing approximately 1% of iron were obtained at 295 and 500 K. Room temperature (RT) spectra of both blue and green samples showed the presence of an asymmetric Fe2+ doublet (ΔE
Q~2.7 mm/s, δ~1.1 mm/s), with a very broad low-velocity peak. There is no clear evidence for the presence of a ferric component. The MS of the yellow sample at RT consists of an intense central absorption with parameters typical for Fe3+ (ΔE
Q~0.4 mm/s, δ~0.29 mm/s), plus an apparently symmetrical Fe2+ doublet. This sample acquires a light-blue shade upon heating in air at about 620 K. Thermal treatments at high temperatures caused no significant changes in the MS, but the green and yellow beryl acquire a blue colour. All these results are interpreted in relation to the existence of channel water and the distribution of iron among the available crystallographic sites. 相似文献
24.
E. M. Chamorro Pérez I. Daniel J.-C. Chervin P. Dumas J. D. Bass T. Inoue 《Physics and Chemistry of Minerals》2006,33(7):502-510
High-pressure synchrotron infrared (IR) absorption spectra were collected between 650 and 4,000 cm−1 at ambient temperature for hydrous Mg-ringwoodite (γ-Mg2SiO4) up to 30 GPa. The main feature in the OH− stretching region is an extremely broad band centred at 3,150 cm−1. The hydrogen bond is strong for most protons and the most probable site for protonation is the tetrahedral edge. With increasing pressure, this band shifts downward while decreasing its integrated intensity until disappearance at a pressure of 25 GPa. Only one band at 2,450 cm−1 and an absorption plateau persist with a maximum wavenumber of 3,800 cm−1. This behaviour is reversible upon pressure release. We interpret this as a second-order phase transition occurring in hydrated Mg-ringwoodite at high pressure (beyond ∼ 25 GPa). This result is compatible with the observation by Kleppe et al. (Phys Chem Miner 29:473–476, 2002a) who suggested the presence of Si–O–Si linkages and/or partial increase in the coordination of Si. Beyond the phase transition, the protons are delocalized and their environment on the ringwoodite structure is probably quite different from that at low pressure. Data obtained in situ at high pressures and temperatures are needed to better understand the effect of protonation on the structure and to better constrain this phase transition. 相似文献
25.
大别山及苏鲁地区微粒金刚石分类及其大地构造意义 总被引:3,自引:1,他引:3
1992年发现大别山首例微粒金刚石之后,又于2003年和2004年在大别山和苏鲁地区的榴辉岩薄片中和榴辉岩的人工重砂中发现了微粒金刚石。本文报道其中尚未发表的7颗,并对2颗较大的薄片中的微粒金刚石和2颗自由晶体金刚石进行拉曼光谱和红外光谱测试。研究结果表明,本区所有微粒金刚石都为IaA和IaB型金刚石的混合体。缺少Ib型金刚石,表明没有人造金刚石的混入。薄片中的金刚石大部分为石榴子石的包裹体,少数产出于颗粒之间,直径为30-180μm。自由颗粒微粒金刚石直径为400-700μm。在大别山北部,不但又一次找到了微粒金刚石,还在石榴子石中发现有单斜辉石、磷灰石和金红石的出溶。这表明北大剐不但是超高压地质体,而且可能是本区俯冲最深的地质体。 相似文献
26.
T. Geisler 《Physics and Chemistry of Minerals》2002,29(6):420-429
Raman spectroscopy and the powder diffraction technique have been used to monitor the recovery process of two partially metamict
zircons (2.6 and 4.8 × 1018
α-decays g−1) from Sri Lanka during a series of isothermal annealing experiments in the temperature range from 870 to 1622 K. These experiments
show for the first time that structural recovery in partially metamict zircon proceeds via three distinct recovery stages,
each of which occurs within a distinct time-temperature regime. Whereas the first two stages have previously been recognized
(recovery of damaged crystalline remnants and epitaxial recrystallization), the third stage has not yet been identified as
a single activated process. It is suggested that anisotropic defect annealing during the first stage at low temperatures,
where the structure recovers preferentially along the a(b) plane, produces a geometrical situation where large structural rearrangements are necessary to remove the remaining defects
inside the crystalline material. This situation is approximately reached when the amorphous domains start to recrystallize.
The reason for anisotropic annealing can be found in a different connectivity between polyhedral linkages in both directions
of the zircon lattice. High apparent activation energies, in the range of 6.4 to 7.9 eV, were determined for the third recovery
stage from the Raman data, which are interpreted to reflect large structural rearrangements (i.e. polyhedral tilting) associated
with the final recovery of the c axis. This explains the occurrence of a distinct recrystallization stage without defect annealing. Finally, it should be
mentioned that the first recovery stage is not necessarily expected to occur in less damaged zircon crystals (<∼2 × 1018
α-decays g−1), since less stable defects along the basal plane might have already been self-annealed during radiation damage accumulation
under ambient temperatures.
Received: 6 September 2001 / Accepted: 25 February 2002 相似文献
27.
G. M. da Costa E. Van San E. De Grave R. E. Vandenberghe V. Barrón L. Datas 《Physics and Chemistry of Minerals》2002,29(2):122-131
A novel method for synthesis of aluminium hematites, based upon the homogeneous precipitation of Fe and Al oxinates in various proportions, is presented. The precursor precipitates are heated in air at 700?°C. X-ray diffraction, thermal analyses, BET, FTIR, optical reflection analysis, TEM and Mössbauer spectroscopy at room temperature and 80?K of the resulting products indicate that single-phase hematites are formed with structural Al substitution of up to 10 at%. Interestingly, the particle size (>100?nm) is not substantially reduced by the Al content. Although it remains difficult to obtain a homogeneously distributed Al substitution in the final hematite, this processing line offers a unique opportunity to separate the effects of grain size and Al substitution on the Morin transition temperature (T M) of Al hematite. From the comparison between the present hematites and a series of Al-substituted hematites with lepidocrocite as precursor, it could be shown that the effect on T M, associated with a change of a factor 10 in grain size, is about 1/3 of the effect caused by a change of 10 in the degree of substitution. Finally, it is suggested that proper thermal treatments under different conditions of the same precursors are likely to produce spinel phases. 相似文献
28.
Raman spectra of diopside were collected from atmospheric pressure to 71 GPa. The pressure dependences of 22 modes were determined.
Changes occurred in the spectra at three different pressures. First, at approximately 10 GPa, the two Raman modes at 356 and
875 cm−1 disappeared, while the mode at 324 cm−1 split into two modes, diverging at this pressure with significantly different pressure shifts; second, at approximately 15
GPa, a small (1 to 2 cm−1) drop in several of the frequencies was observed accompanied by changes in the pressure dependency of some of the modes;
and third, above 55 GPa, the modes characteristic of chains of tetrahedrally coordinated silicon disappeared, while those
for octahedrally coordinated silicon appeared. The first change at 10 GPa appears to be a C2/c to C2/c transition involving a change in the Ca coordination. The third change above 55 GPa appears to be a change in the silicon
coordination. At 15 GPa, it is suggested that a change in compressional mechanism takes place.
Received: 14 November 2000 / Accepted: 9 January 2002 相似文献
29.
M. A. Bouhifd G. Gruener B. O. Mysen P. Richet 《Physics and Chemistry of Minerals》2002,29(10):655-662
Premelting effects in gehlenite (Ca2Al2SiO7) have been studied by Raman spectroscopy and calorimetry, and in gehlenite and pseudowollastonite (CaSiO3) by electrical conductivity. The enthalpy of premelting of gehlenite is 17.3 kJ mol−1 and represents 9% of the reported enthalpy of fusion, which is in the range of the reported fraction of other minerals. The
Raman and electrical conductivity experiments at high temperatures, for gehlenite and pseudowollastonite, show that the premelting
effects of both compositions are associated with enhanced dynamics of calcium atoms near the melting point. This conclusion
agrees with the results obtained for other minerals like diopside, but contrasts with those found for sodium metasilicate
in which the weaker bonding of sodium allows the silicate framework to distort near the melting temperature and deform in
such a way to prefigure the silicate entities present in the melt.
Received: 30 April 2002 / Accepted: 7 August 2002
Acknowledgements We thank Y. Linard for help with DSC measurements and two anonymous reviewers for their constructive comments. This work
has been partly supported by the EU Marie-Curie fellowship contract no. HPMF-CT-1999-00329, the CNRS-Carnegie Institution
of Washington program PICS no.192, and the NSF grants EAR-9614432 and EAR-9901886 to B.O.M. 相似文献
30.
TH. Blumenstock H. Fisher A. Friedle F. Hase P. Thomas 《Journal of Atmospheric Chemistry》1997,26(3):311-321
During SESAME phase I ground-based FTIR measurements were performed atEsrange near Kiruna, Sweden, from 28 January to 26 March 1994. Zenith columnamounts of ClONO2, HCl, HF, HNO3,O3, N2O, CH4, and CFC-12 werederived from solar absorption spectra. Time series of ClONO2and HCl indicate a chlorine activation at the end of January and around 1March. On 1 March a very low amount of HCl of 2.09times; 1015molec. cm-2 was detected, probably caused by a second chlorineactivation phase starting from an already decreased amount of HCl. The ratioof column amounts of HCl to ClONO2 decreased inside the vortexfrom about 1 in January to 0.4 in late March compared to values of about 2outside the vortex. Although the Arctic stratosphere was rather warm in winter1993/94 and PSCs occurred seldom, chlorine partitioning into its reservoirspecies HCl and ClONO2 changed during that winter andClONO2 is the major chlorine reservoir at the end of thewinter as in cold winters like 1991/92 and 1994/95. 相似文献