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51.
俞志尧 《中国科学院上海天文台年刊》2005,(1):95-102
到目前为止已发现了106个OH megamaser源。经典的OH megamaser模型给出宿主星系的强的远红外辐射抽运非饱和的OH megamaser。抽运效率(S1667/S60)对于非饱和OH megamaser及其宿主星系来说是一个重要的物理参数。研究了什么物理量与抽运效率有关,得到无论OH megam aser的光度还是OH megamaser 1667MHz的流量密度都与抽运效率相关。但是主线强度比,主线 1667MHz的光学深度绝对值,主线1665MHz的流量密度均与抽运效率不相关。 相似文献
52.
本文计算了一批OH/IR星的绝对K星等Mk,对OH/IR星的Mk和距离d作了讨论。发现当K较亮时,Mk为一常数;当K较暗时,Mk较离散且呈现一定的变化趋势。本文还拟合得到了一个由K星等求距离的经验公式,并由此公式计算了一批OH/IR星的距离。最后,对所得结果进行了解释和讨论。 相似文献
53.
K.-Y. Wang J. A. Pyle D. E. Shallcross S. M. Hall 《Journal of Atmospheric Chemistry》2001,40(2):123-170
In part 3 of this series of papers on a new 3-D global troposphericchemical transport model, using an Integrated Modelling System (IMS), anevaluation of the model performance in simulating global distributions andseasonal variations for volatile organic compounds (VOCs) in the atmosphere,is presented. Comparisons of model OH concentrations with previous modelstudies show consistent modelled OH levels from the subtropics tomidlatitudes, while more discrepancies occur over the tropical lowlatitudes, with IMS predicting the highest levels of OH. The close agreementbetween modelled OH concentrations over midlatitudes, where high surfaceNOxand VOC concentrations are also found, is indicative of the strongphotochemical coupling between NOx, VOCs and O3 overthese latitudes. IMSOH concentrations in the Northern Hemisphere (NH) midlatitudes during summerare generally lower than available measurements, implying that models ingeneral are underestimating OH levels at this location and time of year.Substantial differences between model OH concentrations over low latitudesclearly highlight areas of uncertainty between models. IMS OH concentrationsare the highest in general of the models compared, one possible reason isthat biogenic emissions of species such as isoprene and monoterpenes arehighest in IMS, leading to higher O3 levels and hence higher OH.Generally, the IMS VOC concentrations show a similar seasonality to themeasurements at most locations. In general though, IMS tends to underestimatethe NH wintertime VOC maximum and overestimate the NH summertime VOCminimum. Such an overestimate in summer could be due to IMSunderestimating OH levels, or an overestimation of VOC emissions or possiblya problem with model transport, all of these possibilities are explored.Except for n-pentane, the model underprediction of a VOC maximum during theNH winter month strongly suggests a missing emission mechanism in the modelor an underestimate of an existing one. It is very likely that there is alack of time varying emission sources in the model to account for theseasonal change in emission behaviour such as increasing energy usage (e.g.,electricity and gas), road transportation, engine performance, and otheranthropogenic factors which show strong seasonal characteristics. Theanomalous overprediction of wintertime n-pentane compared with its closesummertime prediction with the measurements suggest that emissions in thiscase may be too high. 相似文献
54.
N. R. Khisina R. Wirth M. Andrut A. V. Ukhanov 《Physics and Chemistry of Minerals》2001,28(5):291-301
Olivine crystals from two mantle nodules in kimberlites (pipe Udachnaya and pipe Obnazennaya, Yakutiya, Siberia) were investigated using EMP, TEM, AEM and FTIR techniques to determine the mode of hydrogen occurrence in olivine. Olivine contains three types of nanometer-sized inclusions: “large” inclusions of hexagonal-like shape up to several hundred nm in size (1), lamellar defects (2) and small inclusions of hexagon-like shape up to several 10?nm in size (3). Lamellar defects and small inclusions are considered to be a “hydrous” olivine. All three types of inclusions contain OH? or water, but they are different with respect to their phase composition. In “large” inclusions (1) hydrous magnesium silicates, such as serpentine?+?talc (“kerolite”?) and 10-Å phase?+?talc were identified. Lamellar defects (2) and small inclusions (3) are depleted in Mg and Fe compared to the olivine matrix, while the silica content is the same as that of olivine. Modulations in the periodicity of the olivine structure are observed in SAED patterns and HREM images of (2) and (3). The superperiodicity can be referred to OH?-bearing point defect ordering in the olivine structure. If this is the case, the material of both lamellar defects and small inclusions can be assumed to be a “hydrous olivine” Mg2– x v x SiO4H2 x with a cation-deficient olivine crystal structure. Thus, both an extrinsic mode of hydrogen occurrence in olivine, such as nanometer-sized inclusions of OH?-bearing magnesium silicates, and an intrinsic mode of hydrogen incorporation into the olivine structure, such as “hydrous olivine” in itself, were found. The data obtained here show that the OH absorption bands observed in olivine spectra at 3704(3717) and 3683(3688) cm?1 can be unambiguously identified with serpentine; the band at 3677(3676) cm?1 can be associated with talc. The absorption bands observed at 3591 and 3660?cm?1 in olivine match those of the 10-Å phase at 3594, 3662 and 3666?cm?1. 相似文献
55.
Jarken Esimbek 《中国天文和天体物理学报》2005,5(5):557-562
A maser spectral line system is newly implemented on the Urumqi 25m Radio Telescope. The system consists mainly of a cooling receiver and a 4096 channels digital correlation spectrometer. The frequency resolution of the spectrometer at the maximum signal bandwidth of 80MHz is 19.5kHz. After careful calibrations observation at the 1665 MHz OH maser emission was made towards a number of sources, including W49N and W75N. The observed results demonstrate that the digital correlation spectrometer is suitable for astronomical spectral line observations. 相似文献
56.
Jarken Esimbek 《中国天文和天体物理学报》2010,10(2)
We collect 3249 OH maser sources from the literature published up to April 2007, and compile a new catalog of OH masers. We look for the exciting sources of these masers and their infrared properties from IRAS and MSX data, and make a statistical study. MSX sources associated with stellar 1612 MHz OH masers are located mainly above the blackbody line; this is caused by the dust absorption of stellar envelopes, especially in the MSX A band. The mid-IR sources associated with stellar OH masers are concentrate... 相似文献
57.
Y. ?KudohEmail author T. ?Kuribayashi A. ?Suzuki E. ?Ohtani T. ?Kamada 《Physics and Chemistry of Minerals》2004,31(6):360-364
The space group and hydrogen positions of -(Al0.84Mg0.07Si0.09)OOH are investigated using a single crystal synthesized using a multi-anvil apparatus under conditions of 1000 °C and 21 GPa. The space group determined by single-crystal X-ray diffraction is to Pnn2, with unit-cell parameters of a=4.6975(8) Å, b= 4.2060(6) Å, c=2.8327(4) Å, and V=55.97(1) Å3. Partial occupancy of the Al site by Mg and Si suggests the possibility of a limited solid solution between -AlOOH, stishovite, and a hypothetical CaCl2-type Mg(OH)2 that is 16% denser than brucite. Difference-Fourier maps reveal two small but significant Fourier peaks attributable to hydrogen atoms. Atomic distances and angles around the first peak indicate a hydrogen bond with O···O distances of 2.511 Å, while those around the second peak are suggestive of a bifurcated hydrogen bond with O···O distances of 2.743 and 2.743 Å. 相似文献
58.
R. Iannone R. S. Anderson A. Vogel J. Rudolph P. Eby M. J. Whiticar 《Journal of Atmospheric Chemistry》2004,47(2):191-208
The hydrogen kinetic isotope effects (KIEs) of the reactions of 15 non-methane hydrocarbons (NMHCs) with the OH radical were measured at 298 ± 2 K. The measurements were made using NMHCs without artificial isotopic labeling or enrichment. The following average hydrogen KIE values, in per mil (), were obtained: 29.8 ± 2.1 (toluene),51.6 ± 2.1 (n-butane), 97.3± 12.5 (i-butane), 63.2 ± 5.9 (cyclopentane), 10.5 (p-xylene), 26.8 ± 3.5 (ethylbenzene), 65.9± 7.0 (n-pentane), 79.5 ± 9.6 (cyclohexane), 52.8 ± 5.0(n-hexane), 38.9 ± 7.8 (n-heptane), 33.4 ± 3.1 (n-octane), 29.6 ± 1.6(n-nonane), and 29.0 ± 5.3 (n-decane). The KIEs for reactions of two alkenes (cyclohexene and 1-heptene) could not be determined accurately due to interference from reaction with ozone, but nevertheless the results clearly show that the KIEs for reaction of alkenes with OH are significantly lower than those for saturated hydrocarbons. The KIEs for reaction of alkanes are smaller than isotope effects reported in literature for the reactions of NMHCs artificially labeled with deuterium. The main reason for this difference is the reduced probability for reaction at a labeled site for compounds with close to natural deuterium abundance, although some impact of secondary isotope effects cannot be ruled out. Still, the KIEs for NMHCs with natural or close to natural abundance of deuterium are of sufficient magnitude to allow determination of the extent of chemical processing of hydrocarbons in the atmosphere using methods analogous to stable carbon KIE studies. Furthermore, it is shown that combining stable hydrogen and stable carbon isotope ratio data has the potential to also provide valuable information regarding the stable isotope ratios of emissions, and specifically to test one of the key assumptions of the stable isotope hydrocarbon clock, the absence of significant variations of the stable isotope ratio for the emitted NMHCs. 相似文献
59.
Estelle Turpin Christa Fittschen Alexandre Tomas Pascal Devolder 《Journal of Atmospheric Chemistry》2003,46(1):1-13
We have determined the 2-oxo-propyl CH3C(O)CH2 (sometimes called 1-methylvinoxy or acetonyl) radical yield for the reaction of acetone with OH radical relative to the 2-oxo-propyl yields for the reactions of F- and Cl atoms with acetone using the Discharge Flow technique. The 2-oxo-propyl radical has been monitored by Laser Induced Fluorescence LIF at short reaction times in the systems: OH + acetone (R1), F + acetone (R2), and Cl + acetone (R3). From these measurements we have deduced the branching ratio for the 2-oxo-propyl radical formation in the title reaction to be in the range 0.8 R 1. 相似文献
60.
Xinrong Ren Hartwig Harder Monica Martinez Ian C. Faloona David Tan Robert L. Lesher Piero Di Carlo James B. Simpas William H. Brune 《Journal of Atmospheric Chemistry》2004,47(2):169-190
Accurate OH and HO2 (collectively called HOx) measurements by laser-induced fluorescence (LIF) may be contaminated by spurious signals from interfering atmospheric chemicals or from the instrument itself. Interference tests must be conducted to ensure that observed OH signal originates solely from ambient OH and is not due to instrument artifacts. Several tests were performed on the Penn State LIF HOx instrument, both in the laboratory and in the field. Theseincluded measurements of the instrument's zero signal by using either zero air or perfluoropropylene to remove OH, examination of spectral interferences from naphthalene, sulfur dioxide, and formaldehyde, and tests of interferences by addition of suspected interfering atmospheric chemicals, including ozone, hydrogen peroxide, nitrous acid, formaldehyde, nitric acid, acetone, and organic peroxy radicals (RO2). All tests lacked evidence ofsignificant interferences for measurements in the atmosphere, including highly polluted urban environments. 相似文献