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51.
《International Journal of Digital Earth》2013,6(12):1214-1230
ABSTRACTEarth observation data are typically compressed using general-purpose single-threaded compression algorithms that operate at a fraction of the bandwidth of modern storage and processing systems. We present evidence that recently developed multi-threaded compression codecs offer substantial benefits over widely used single-threaded codecs in terms of compression efficiency when applied to a selection of moderate resolution imaging spectroradiometer (MODIS) datasets stored in the HDF5 format. Compression codecs from the LZ77 and Rice families are shown to vary in efficacy when applied to different MODIS data products, highlighting the need for compression strategies to be tailored to different classes of data. We also introduce LPC-Rice, a new multi-threaded codec, that performs particularly well when applied to time-series data. 相似文献
52.
53.
Malorie Dierick Éric Pili Nelly Assayag Pierre Agrinier 《Geostandards and Geoanalytical Research》2017,41(3):397-409
A new method for accurate determination of oxygen isotopes in uranium oxides encountered in the nuclear fuel cycle was developed using the conventional BrF5 fluorination technique. Laser‐assisted fluorination was tested for comparison. We focused on fine powders of triuranium octoxide (U3O8), uranium dioxide (UO2±x with 0 ≤ x ≤ 0.25), uranium trioxide (UO3.nH2O, with 0.8 ≤ n ≤ 2) and diuranates (M2U2O7.nH2O, with M = NH4, Na or Mg0.5 and 0 ≤ n ≤ 6). Fluorination at room temperature and heating under vacuum at 150 °C are shown to eliminate both adsorbed and structural water from the powder samples. Precision fit for purpose of δ18O values (± 0.3‰, 1s) and oxygen yields (close to 100%) were obtained for U3O8 and UO2 where oxygen is only bound to uranium. A lower precision was observed for UO3.nH2O and M2U2O7.nH2O where oxygen is both present in the structural H2O and bonded to uranium and where the extracted O2(g) can be contaminated by NF3 and NOx compounds. Laser‐assisted fluorination gave shifted δ18O values between +0.8 and +1.4‰ for U3O8, around ?0.8‰ for UO3.nH2O and between ?3.9 and ?4.5‰ for M2U2O7.nH2O (± 0.3‰, 1s) compared with the conventional method. 相似文献
54.
Gianluca Iezzi Mario Tribaudino Giancarlo Della Ventura Fabrizio Nestola Fabio Bellatreccia 《Physics and Chemistry of Minerals》2005,32(7):515-523
The synthetic amphibole Na0.95(Li0.95Mg1.05)Mg5Si8O22(OH)2 was studied in situ at high-T, using IR OH-stretching spectroscopy and synchrotron X-ray powder diffraction. At room-T the sample has P21
/m symmetry, as shown by the FTIR spectrum. It shows in the OH region two well-defined and intense absorptions at 3,748 and
3,712 cm−1, respectively, and two minor bands at 3,667 and 3,687 cm−1. The main bands are assigned to the two independent O–H groups in the primitive structure. The two minor bands evidencing
the presence of small amount of vacant A-site (A□0.05). With increasing T, these bands shift continuously and merge into a unique absorption at high temperature. A change as a function of increasing
T is revealed by the evolution of the refined unit-cell parameters, whose trend shows a transition to C2/m at about 320–330°C. The spontaneous scalar strain, fitted with a tricritical 2–6 Landau potential, gives a T
c of 325(10)°C (β parameter = 0.27). Comparison with the second-order P21
/m ⇔ C2/m phase transition at 255°C for synthetic amphibole ANa0.8B(Na0.8Mg1.2)CMg5Si8O22(OH)2 indicates that the substitution of Na with Li at the B-sites strongly affects the thermodynamic character and the T
c of the phase transition. The comparison of LNMSH amphiboles with cummingtonitic ones shows that the high-T thermodynamic behaviour is affected by A-site occupancy. 相似文献
55.
Jia?RongfenEmail author Peng?Xianzhi Zhou?Zheng Liu?Dehan Wang?Guanxin Wang?Deqiang 《中国地球化学学报》2004,23(3):197-206
Relatively strongly magnetic fine components (< 30μm, XS-4J and DS-4J) which are most environmentally sensitive were separated from layer S5-1 in the Xifeng and Duanjiapo loess sections and analyzed by MPV-3 for their morphometric characteristics and reflectance, SEM-ESD for their element contents and XRD for their mineral phases, respectively. The results showed that minerals in both samples are dominated by detrial Fe-Ti oxides of aeolian origin. In sample XS-4J the reflectance and iron contents of magnetic minerals are usually high. In addition to magnetite (Fe3O4), maghemite (γFe2O3) and hematite (Fe2O3), some Fe-high oxide (72.25 wt%–86.67 wt%), ilmenite (FeTiO3), and magnetite-ulvöspinel [Fe(FeCr)O4, Fe (FeNi)O4] were also detected. In sample DS-4J obvious negative linear correlations were found between Ti and Fe, and the contents of Mn, Si, Al and Ca are usually high and the minerals are dominated by magnetite (maghemite), goethite (FeOOH) and limonite (containing Si and OH). In addition, the signs of corrosion of magnetic minerals and newly crystallized magnetite (maghemite) were recognized. Differences in the composition and assemblage characteristics of magnetite minerals between XS and DS reflect significant differences in source rocks and preserving conditions. 相似文献
56.
本文研究了钴(Ⅱ)-5-Br-PADNm络合物的光度性质。在pH5.0缓冲溶液中,有TritonX-100存在时,Co~(2 )与5-Br-PADNm形成1:2红色络合物,λ_(max)为547nm,ε为1.35×10~5l·mol~(-1)·cm~(-1)。所提出的方法用于矿石及茶叶中Co的测定,得到满意结果。 相似文献
57.
By compiling wide-angle seismic velocity profiles along the 400-km-long Lofoten–Vesterålen continental margin off Norway, and integrating them with an extensive seismic reflection data set and crustal-scale two-dimensional gravity modelling, we outline the crustal margin structure. The structure is illustrated by across-margin regional transects and by contour maps of depth to Moho, thickness of the crystalline crust, and thickness of the 7+ km/s lower crustal body. The data reveal a normal thickness oceanic crust seaward of anomaly 23 and an increase in thickness towards the continent–ocean boundary associated with breakup magmatism. The southern boundary of the Lofoten–Vesterålen margin, the Bivrost Fracture Zone and its landward prolongation, appears as a major across-margin magmatic and structural crustal feature that governed the evolution of the margin. In particular, a steeply dipping and relatively narrow, 10–40-km-wide, Moho-gradient zone exists within a continent–ocean transition, which decreases in width northward along the Lofoten–Vesterålen margin. To the south, the zone continues along the Vøring margin, however it is offset 70–80 km to the northwest along the Bivrost Fracture Zone/Lineament. Here, the Moho-gradient zone corresponds to a distinct, 25-km-wide, zone of rapid landward increase in crustal thickness that defines the transition between the Lofoten platform and the Vøring Basin. The continental crust on the Lofoten–Vesterålen margin reaches a thickness of 26 km and appears to have experienced only moderate extension, contrasting with the greatly extended crust in the Vøring Basin farther south. There are also distinct differences between the Lofoten and Vesterålen margin segments as revealed by changes in structural style and crustal thickness as well as in the extent of elongate potential-field anomalies. These changes may be related to transfer zones. Gravity modelling shows that the prominent belt of shelf-edge gravity anomalies results from a shallow basement structural relief, while the elongate Lofoten Islands belt requires increased lower crustal densities along the entire area of crustal thinning beneath the islands. Furthermore, gravity modelling offers a robust diagnostic tool for the existence of the lower crustal body. From modelling results and previous studies on- and off-shore mid-Norway, we postulate that the development of a core complex in the middle to lower crust in the Lofoten Islands region, which has been exhumed along detachments during large-scale extension, brought high-grade, lower crustal rocks, possibly including accreted decompressional melts, to shallower levels. 相似文献
58.
传统的Fenton均相亚铁盐催化剂处理染料废水,具有难以避免的二次污染和亚铁离子流失问题。分子筛催化剂相比传统催化剂具有高效环保的特点,在催化氧化染料废水领域有着良好的前景。本文通过液相离子交换法制备了Fe-ZSM-5非均相分子筛催化剂,替代传统的亚铁盐催化剂,应用X射线衍射对制备的Fe-ZSM-5分子筛催化剂进行表征,表明随离子交换次数的增加,Fe-ZSM-5催化剂负载的铁量上升,且较好地保持了分子筛结构,有利于提高亚铁离子的催化能力。通过实验确定了Fe-ZSM-5催化剂催化反应的最佳温度、pH值、Fe-ZSM-5的用量、反应时间等工艺参数,比较了Fe-ZSM-5催化剂和传统Fenton均相催化剂降解染料废水的脱色率和废水中铁离子的残留量,结果表明Fe-ZSM-5的脱色率达到98.5%,相比于Fenton均相催化剂的脱色率提升约3%;两种催化剂的铁离子残留量差别显著,Fe-ZSM-5催化剂处理的废水中只产生微量的Fe离子,可以认为Fe-ZSM-5非均相分子筛催化剂有效地解决了催化剂损耗和二次污染问题。 相似文献
60.