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91.
蒙古高原包括蒙古全部、俄罗斯南部和中国北部部分地区。蒙古高原的土地利用/覆盖格局与变化,对揭示该区域乃至整个东北亚地区的资源、环境和生态特征,促进该区域可持续发展具有重要的现实和科学意义。本文以在蒙古国中央省及其所含首都乌兰巴托市为研究区,利用空间分辨率为30 m的TM影像,采取QUEST(Quick Unbiased and Efficient Statistical Tree)决策树方法,通过图像目视解译,获取了研究区2010年土地覆盖分类数据。结果显示,草地占据研究区总面积的70.88%,其次是森林占14.83%、裸地占10.73%、农田占2.98%、水体占0.31%、建筑用地占0.27%、湿地占0.02%。通过野外实地采集的139个GPS验证点进行精度评价发现,一级土地覆盖类型的总体精度可达72.66%。针对草地的二级分类的总体精度有较明显下降,其主要是由于中蒙科学家对于草地类型分类体系的差异所造成的典型草地和荒漠草地的混分。 相似文献
92.
93.
Abstract A modified response analysis in the form of an orthotide parametrization is used to derive major semi‐diurnal and diurnal tidal constituents over the Newfoundland and Scotian Shelves from TOPEX/POSEIDON altimeter data. The orthotide formulation simultaneously solves for eight major semi‐diurnal and diurnal constituents, and has an accuracy of better than ~1.5 cm for each constituent. Tidal elevations are derived from the altimeter data on the ascending and descending satellite ground tracks, and interpolated using the method of statistical interpolation. The semi‐diurnal constituents (M2, S2 and N2) compare favourably with available in‐situ observations and a numerical model. The diurnals (K1 and O1) are not as accurate as the semi‐diurnals, especially in the nearshore environment. The paper demonstrates the ability of TOPEX/POSEIDON altimetry to provide accurate tidal data over a continental shelf. 相似文献
94.
Friedrich Hörz Mark J. Cintala Thomas H. See Keiko Nakamura‐Messenger 《Meteoritics & planetary science》2009,44(9):1243-1264
Abstract— We conducted impact experiments into SiO2‐based aerogel of uniform density (0.02 g cm?3) with spherical corundum projectiles. The highly refractory nature and mechanical strength of corundum minimizes projectile deformation and continuous mass loss by ablation that might have affected earlier experiments with soda‐lime glass (SLG) impactors into aerogel targets. We find that corundum is a vastly superior penetrator producing tracks a factor of 2.5 longer, yet similar in diameter to those made by SLG. At velocities <4 km s?1 a cylindrical “cavity” forms, largely by melting of aerogel. The diameter and length of this cavity increase with velocity and impactor size, and its volume dominates total track volume. A continuously tapering, exceptionally long and slender “stylus” emerges from this cavity and makes up some 80–90% of the total track length; this stylus is characterized by solid‐state deformations. Tracks formed below 4 km s?1 lack the molten cavity and consist only of a stylus. Projectile residues recovered from a track's terminus substantially resemble the initial impactors at V > 4 km s?1, yet they display two distinct surfaces at higher velocities, such as a blunt, forward face and a well‐preserved, hemispherical trailing side; a pronounced, circumferential ridge of compressed and molten aerogel separates these two surfaces. Stringers and patches of melt flow towards the impactor's rear where they accumulate in a characteristic melt tip. SEM‐EDS analyses indicate the presence of Al in these melts at velocities as low as 5.2 km s?1, indicating that the melting point of corundum (2054 °C) was exceeded. The thermal model of aerogel impact by Anderson and Cherne (2008) suggests actual aerogel temperatures <5000 K at comparable conditions. We therefore propose that projectile melting occurs predominantly at those surfaces that are in contact with this very hot aerogel, at the expense of viscous heating and associated ablation. Exposure to superheated aerogel may be viewed as extreme form of “flash heating.” This seems consistent with observations from the Stardust mission to comet Wild 2, such as relatively pristine interiors of rather large, terminal particles, yet total melting of most fine‐grained dust components. 相似文献
95.
We examined As concentration, mineralogical site, and oxidation state in the serpentinites associated with the Tso Morari eclogitic rocks in the Indus suture zone, northwest Himalaya, to examine how highly fluid-soluble elements like As are transferred from slabs to arc magmas in subduction zones. The serpentinite samples represent hydrated peridotites at the base of the mantle wedge beneath Eurasia, and were exhumed from a depth of ∼100 km during subduction of the Indian continental margin. The bulk serpentinite samples contain total As concentrations ranging from 6 to 275 ppm. Arsenic in the samples is most likely present with magnetite and antigorite, since electron probe analysis yielded up to 90 ppm As in these minerals. X-ray absorption near-edge structure spectra indicate that As in serpentinites is mostly As(V) and that the neighboring atoms of As are O, although there are minute grains of sulfides and arsenides. The ratio of As(V) to total As is greater in samples with higher As contents, suggesting that the major source of As was oxidized As(V), introduced to the mantle wedge. Arsenic(V), originally adsorbed on Fe-oxides in slabs and overlying sediments, was most likely liberated during their subduction and incorporated subsequently in the overlying mantle wedge. Our data constrain the introduction of As into the mantle wedge at relatively shallow levels, much shallower than 25 km. Arsenic incorporated in the serpentinites was transported to deeper levels by mantle flow downward along the subduction zone, to be subsequently exhumed together with eclogitic rocks. 相似文献
96.
Yoshio Takahashi Tomoya Uruga Hajime Tanida Keiko H. Hattori 《Geochimica et cosmochimica acta》2007,71(21):5180-5190
Local atomic structures of Re and radiogenic Os in molybdenite from the Onganja mine, Namibia, were examined using X-ray absorption fine structure (XAFS). Rhenium LIII-edge X-ray absorption near-edge structure (XANES) and extended X-ray absorption fine structure (EXAFS) show that the oxidation state of Re, the interatomic distances between Re and the neighboring atoms, and the coordination number of Re to S are very similar to those of Mo in molybdenite. The results confirm that Re is present as Re(IV) in the Mo site in molybdenite.Measurement of LIII-edge XANES and EXAFS of a minor concentration (8.55 ppm) of radiogenic Os was accomplished in fluorescence mode by removing the interfering X-rays from Re and other elements using a crystal analyzer system. The data indicate that the oxidation state of radiogenic Os is Os(III) and Os(IV) and clearly different from Os(II) in natural sulfide minerals, such as OsS2 (erlichmanite). XANES data also suggest that radiogenic Os does not form a secondary Os phase, such as OsS2 or Os metal, in molybdenite.EXAFS of radiogenic Os was successfully simulated assuming that Os is present in the Mo site in molybdenite. The data are consistent with the XANES data; Os does not form Os phases in molybdenite. The EXAFS simulation showed that the interatomic distance between Os and S is 2.27 Å, which is 0.12 Å smaller than the distances of Re-S and Mo-S (2.39 Å) in molybdenite. Similar valences and ionic sizes of Re and Mo in molybdenite support the fact that large amounts of Re can be incorporated into the Mo site as has been observed in previous studies, whereas the different properties of Os compared to Mo and Re suggested here support much lower abundance of common Os in molybdenite. This makes molybdenite an ideal mineral for the Re-Os geochronometer as shown in many studies. However, the shorter distance between radiogenic Os and S compared to those of Re-S and Mo-S in molybdenite suggests that the radiogenic Os has a smaller ionic size than Re(IV) and Mo(IV). Furthermore, Os may be partly present as Os(III). Smaller and lower charge Os can diffuse faster than larger and higher charge Re in molybdenite at a given set of conditions. Hence, our study provides an atomic-level explanation for the high mobility of Os compared to Re, which has been suggested by earlier workers using laser ablation ICP-MS. 相似文献
97.
Isotopic compositions were determined for quartz, sericite and bulk rock samples surrounding the Uwamuki no. 4 Kuroko ore body, Kosaka, Japan.
18O values of quartz from Siliceous Ore (S.O.), main body of Black Ore B.O.) and the upper layer of B.O. are fairly uniform, +8.7 to +10.5. Formation temperatures calculated from fractionation of 18O between sericite and quartz from B.O. and upper S.O. are 250° to 300° C. The ore-forming fluids had
18O values of +1 and D values of –10, from isotope compositions of quartz and sericite.Tertiary volcanic rocks surrounding the ore deposits at Kosaka have uniform
18O values, +8.1±1.0 (n=50), although their bulk chemical compositions are widely varied because of different degrees of alteration. White Rhyolite, which is an intensely altered rhyolite occurring in close association with the Kuroko ore bodies, has also uniform
18O values, +7.9±0.9 (n=19). Temperatures of alteration are estimated to be around 300° C from the oxygen isotope fractionation between quartz and sericite. Paleozoic basement rocks phyllite and chert, have high
18O values, +18 and +19. The Sasahata formation of unknown age, which lies between Tertiary and Paleozoic formations, has highly variable
18O, +8 to +16 (n=4). High
18O values of the basement rocks and the sharp difference in
18O at their boundary suggest that the hydrothermal system causing Kuroko mineralization was mainly confined within permeable Tertiary rocks. D values of altered Tertiary volcanic rocks are highly variable ranging from –34 to –64% (n=12). The variation of D does not correlate with change of chemical composition,
18O values, nor distance from the ore deposits. The relatively high D values of the altered rocks indicate that the major constituent of the hydrothermal fluid was sea water. However, another fluid having lower D must have also participated. The fluid could be evolved sea water modified by interaction with rocks and the admixture of magmatic fluid. The variation in D may suggest that sea water mixed dispersively with the fluid. 相似文献
98.
Oxygen and carbon isotope compositions were determined for calcites from the Green Tuff formations of Miocene age in Japan. Values of
18O from 24 calcites in altered rocks from 5 districts range from –2 to +16SMOW, in most cases from 0 to +8SMOW. The low
18O values rule out the possibility of their low-temperature origin or any significant contribution of magmatic fluid in the calcite precipitation. These values, coupled with their mineral assemblages, suggest that the calcites formed from meteoric hydrothermal solutions which caused propylitic alteration after the submarine strata became emergent.Values of
13C from the calcites show a wide variation from –17 to 0PDB. Calcites from different districts have different ranges of
13C values, indicating that there was no homogeneous reservoir of carbon at the time the calcite formed, and that the carbon had local sources. Carbon isotopic compositions of calcite within ore deposits in the Green Tuff formations range from –19 to 0PDB, similar to those of calcite in the altered rocks in the same district, suggesting that the carbon in ore calcites was likely supplied from the surrounding rocks through activity of meteoric hydrothermal solutions. 相似文献
99.
Tadahide Ui Keiko Suzuki-Kamata Rumi Matsusue Kei Fujita Hideya Metsugi Mami Araki 《Bulletin of Volcanology》1989,51(2):115-122
The grain orientations within the matrix of two large-scale welded, two small-scale nonwelded and two nonwelded low-aspect ratio pyroclastic flow deposits are measured to analyze flow behavior. Preferred grain alignments are especially apparent in the middle part of layer 2 of each deposit. Preferred grain alignments do not vary laterally within a 10 m interval. The grain alignments obtained are radial from the source caldera, especially in proximal to medial and plateau-forming facies of pyroclastic flow deposits. Grain alignments are controlled by valley-channel directions for the valley-ponded facies of pyroclastic flow deposits, especially at medial to distal locations. Such local topographic factors strongly affect the data for high-aspect ratio and smallscale deposits, and weakly affect the data for widespread low-aspect ratio pyroclastic flow deposits. This work suggests that grain alignment analysis should be used with care when attempting to determine the location of an unknown source. 相似文献
100.