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11.
The dynamics of photoevaporated molecular clouds is determined by the ablative pressure acting on the ionization front. An important step in the understanding of the ensuing motion is to develop the linear stability theory for an initially flat front. Despite the simplifications introduced by linearization, the problem remains quite complex and still draws a lot of attention. The complexity is related to the large number of effects that have to be included in the analysis: acceleration of the front, possible temporal variation of the intensity of the ionizing radiation, the tilt of the radiation flux with respect to the normal to the surface, and partial absorption of the incident radiation in the ablated material. In this paper, we describe a model where all these effects can be taken into account simultaneously, and a relatively simple and universal dispersion relation can be obtained. The proposed phenomenological model may prove to be a helpful tool in assessing the feasibility of the laboratory experiments directed towards scaled modeling of astrophysical phenomena. PACS Numbers: 98.38.Dq, 98.38.Hv, 52.38.Mf, 5257.FG, 52.72.+v  相似文献   
12.
We investigate the outflow propagation in the collapsar in the context of gamma-ray bursts (GRBs) with 2D relativistic hydrodynamic simulations. We vary the specific internal energy and bulk Lorentz factor of the injected outflow from non-relativistic regime to relativistic one, fixing the power of the outflow to be 1051erg s−1. We observed the collimated outflow, when the Lorentz factor of the injected outflow is roughly greater than 2. To the contrary, when the velocity of the injected outflow is slower, the expanding outflow is observed. The transition from collimated jet to expanding outflow continuously occurs by decreasing the injected velocity. Different features of the dynamics of the outflows would cause the difference between the GRBs and similar phenomena, such as, X-ray flashes.  相似文献   
13.
Over the past few years, our group has been developing hydrodynamic models to simulate formation of the Eagle Nebula pillars. The true test of any model is, of course, how well it can reproduce the observations. Here, we discuss how we go about testing our models against observations. We describe the process by which we “observe” the model data to create synthetic maps. We show an example of this technique using one of our model runs and compare the resultant synthetic map to the real one.  相似文献   
14.
CS(J=1–0), C34S(J=1–0), and CH3OH(10–00A and E) emission lines in the core region of molecular cloud associated with NGC 7538 have been surveyed at angular resolution of 33. Distribution of CS column density shows two prominent peaks. Both blue and red wings in CS line are most prominent at 30 northwest of IRS 11.Paper presented at the IAU Third Asian-Pacific Regional Meeting, held in Kyoto, Japan, between 30 September–6 October, 1984.This work was carried out under the common use observation program at the Nobeyama Radio Observatory (NRO). NRO, a branch of the Tokyo Astronomical Observatory, University of Tokyo, is a cosmic radio observing facility open to outside users.  相似文献   
15.
White-light observations of the total solar eclipse on 13 November 2012 were made at two sites, where the totality occurred 35 min apart. The structure of the corona from the solar limb to a couple of solar radii was observed with a wide dynamic range and a high signal-to-noise ratio. An ongoing coronal mass ejection (CME) and a pre-CME loop structure just before the eruption were observed in the height range between 1?–?2 R. The source region of CMEs was revealed to be in this height range, where the material and the magnetic field of CMEs were located before the eruption. This height range includes the gap between the extreme ultraviolet observations of the low corona and the spaceborne white-light observations of the high corona, but the eclipse observation shows that this height range is essential for the study of CME initiation. The eclipse observation is basically just a snapshot of CMEs, but it indicates the importance of a continuous coverage of CME observations in this height range in the future.  相似文献   
16.
Gas-liquid chromatographic method byGehrke et al. was applied to the determination of the dissolved proteinaceous substace. Sea-water samples were evaporated in vacuum to the volume of one twentieth of the initial volume and separated from deposited inorganic salt crystals. Thirteen kinds of amino acids except histidine, arginine and cystine were quantitatively determined for artificial sea water containing sixteen standard amino acids with accuracy of about five percent and with yield of 80 to 103 percent. This method has advantage comparing with paper or thin layer chromatography on the precision and comparing with ion-exchange method on sensitivity.The difference of amino acid concentration between the sea-water samples of different depth and different region was observed. The total amounts of dissolved amino acids were found to be between 33 and 92g per liter in sea water of Pacific Ocean taken at the surface to 1,500 m in depth.Contribution No. 41, from The Research Institute of North Pacific Fisheries, Hokkaido University.  相似文献   
17.
The two drill holes, which penetrated sub‐horizontal rare earth element (REE) ore units at the Nechalacho REE in the Proterozoic Thor Lake syenite, Canada, were studied in order to clarify the enrichment mechanism of the high‐field‐strength elements (HFSE: Zr, Nb and REE). The REE ore units occur in the albitized and potassic altered miaskitic syenite. Zircon is the most common REE mineral in the REE ore units, and is divided into five types as follows: Type‐1 zircon occurs as discrete grains in phlogopite, and has a chemical character similar to igneous zircon. Type‐2 zircon consists of a porous HREE‐rich core and LREE–Nb–F‐rich rim. Enrichment of F in the rim of type‐2 zircon suggests that F was related to the enrichment of HFSE. The core of type‐2 zircon is regarded to be magmatic and the rim to be hydrothermal in origin. Type‐3 zircon is characterized by euhedral to anhedral crystals, which occur in a complex intergrowth with REE fluorocarbonates. Type‐3 zircon has high REE, Nb and F contents. Type‐4 zircon consists of porous‐core and ‐rim, but their chemical compositions are similar to each other. This zircon is a subhedral crystal rimmed by fergusonite. Type‐5 zircon is characterized by smaller, porous and subhedral to anhedral crystals. The interstices between small zircon grains are filled by fergusonite. Type‐4 and type‐5 zircon grains have low REE, Nb and F contents. Type‐1 zircon is only included in one unit, which is less hydrothermally altered and mineralized. Type‐2 and type‐3 zircon grains mainly occur in the shallow units, while those of type‐4 and type‐5 are found in the deep units. The deep units have high HFSE contents and strongly altered mineral textures (type‐4 and type‐5) compared to the shallow units. Occurrences of these five types of zircon are different according to the depth and degree of the hydrothermal alteration by solutions rich in F and CO3, which permit a model for the evolution of the zircon crystallization in the Nechalacho REE deposit as follows: (i) type‐1 (discrete magmatic zircon) is formed in miaskitic syenite. (ii) LREE–Nb–F‐rich hydrothermal zircon formed around HREE‐rich magmatic zircon (type‐2). (iii) type‐3 zircon crystallized through the F and CO3‐rich hydrothermal alteration of type‐2 zircon which formed the complex intergrowth with REE fluorocarbonates; (iv) the CO3‐rich hydrothermal fluid corroded type‐3, forming REE–Nb‐poor zircon (type‐4). Niobium and REE were no longer stable in the zircon structure and crystallized as fergusonite around the REE–Nb‐leached zircon (type‐4); (v) type‐5 zircon is formed by the more CO3‐rich hydrothermal alteration of type‐4 zircon, suggested by the fact that type‐4 and type‐5 zircon grains are often included in ankerite. Type‐3 to type‐5 zircon grains at the Nechalacho REE deposit were continuously formed by leaching and/or dissolution of type‐2 zircon in the presence of F‐ and/or CO3‐rich hydrothermal fluid. These mineral associations indicate that three representative hydrothermal stages were present and related to HFSE enrichment in the Nechalacho REE deposit: (i) F‐rich hydrothermal stage caused the crystallization of REE–Nb‐rich zircon (type‐2 rim and type‐3), with abundant formation of phlogopite and fluorite; (ii) F‐ and CO3‐rich hydrothermal stage led to the replacement of a part of REE–Nb–F‐rich zircon by REE fluorocarbonate; and (iii) CO3‐rich hydrothermal stage resulted in crystallization of the REE–Nb–F‐poor zircon and fergusonite, with ankerite. REE and Nb in hydrothermal fluid at the Nechalacho REE deposit were finally concentrated into fergusonite by way of REE–Nb–F‐rich zircon in the hydrothermally altered units.  相似文献   
18.
The pressure dependence of the three lattice parameters and unit cell volume of fayalite (Fe2SiO4 olivine) was determined by X-ray diffraction under hydrostatic pressures up to 70 kbar. In order to eliminate stress inhomogeneity within a composite material consisting of a specimen mixed with an internal-pressure standard, a liquid (1 : 1 mixture of ethanol and methanol) was used as a pressure-transmitting medium. The isothermal bulk modulus calculated on the basis of the second-order Birch-Murnaghan equation of state gives the values K0 = 1.19 ± 0.10 Mbar and K0′ = 7 ± 4, and if we assume K0′ = 5: K0 = 1.24 ± 0.02 Mbar. Three axes of fayalite were found to be compressible in the following order, b >c >a. Comparisons with the results obtained under non-hydrostatic compression are made.  相似文献   
19.
Porphyroclastic diopside in garnet lherzolite from Alpe Arami, Bellinzona, Switzerland includes optically-visible clinoamphibole lamellae with a composition intermediate between pargasite and edenite. X-ray and electron microscopic observations show that the diopside crystal contains sub-microscopic thin clinoamphibole lamellae parallel to (010), which have coherent interfaces to the host. A kind of planar defect parallel to (010) in clinopyroxene structure, as suggested by Chisholm (1973), is shown here to correspond to intercalation of a 9 Å lattice fringe of double-chain structure in the electron micrograph of the diopside. The thin clinoamphibole lamellae are observed to be segregated domains consisting of two and more 9 Å fringes.From the chemical characteristics and textural relations of the development of such clinoamphiboles, the chemical change required to form them is considered to have been caused principally by decreasing solubility of atoms such as Na, Al and Cr in clinopyroxene structure during the retrogressive reequilibration. Also, a possibility of finite solid solution of clinoamphibole in clinopyroxene is discussed.  相似文献   
20.
The Chatree deposit is located in the Loei‐Phetchabun‐Nakhon Nayok volcanic belt that extends from Laos in the north through central and eastern Thailand into Cambodia. Gold‐bearing quartz veins at the Q prospect of the Chatree deposit are hosted within polymictic andesitic breccia and volcanic sedimentary breccia. The orebodies of the Chatree deposit consist of veins, veinlets and stockwork. Gold‐bearing quartz veins are composed mainly of quartz, calcite and illite with small amounts of adularia, chlorite and sulfide minerals. The gold‐bearing quartz veins were divided into five stages based on the cross‐cutting relationship and mineral assemblage. Intense gold mineralization occurred in Stages I and IV. The mineral assemblage of Stages I and IV is characterized by quartz–calcite–illite–laumontite–adularia–chlorite–sulfide minerals and electrum. Quartz textures of Stages I and IV are also characterized by microcrystalline and flamboyant textures, respectively. Coexistence of laumontite, illite and chlorite in the gold‐bearing quartz vein of Stage IV suggests that the gold‐bearing quartz veins were formed at approximately 200°C. The flamboyant and brecciated textures of the gold‐bearing quartz vein of Stage IV suggest that gold precipitated with silica minerals from a hydrothermal solution that was supersaturated by boiling. The δ18O values of quartz in Stages I to V range from +10.4 to +11.6‰ except for the δ18O value of quartz in Stage IV (+15.0‰). The increase in δ18O values of quartz at Stage IV is explained by boiling. PH2O is estimated to be 16 bars at 200°C. The fCO2 value is estimated to be 1 bar based on the presence of calcite in the mineral assemblage of Stage IV. The total pressure of the hydrothermal solution is approximately 20 bars at 200°C, suggesting that the gold‐bearing quartz veins of the Q prospect formed about 200 m below the paleosurface.  相似文献   
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