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31.
Micro-spectroscopic investigations of highly heterogeneous waste repository materials 总被引:1,自引:0,他引:1
A.M. Scheidegger D. Grolimund C.R. Cheeseman R.D. Rogers 《Journal of Geochemical Exploration》2006,88(1-3):59
Assuring safe disposal and long-term storage of radioactive and toxic wastes corresponds to a primary environmental task of present societies. To improve any technical limitation, a mechanistic understanding of the processes governing the binding of heavy metals and radionuclides is required. In this study, the significance of synchrotron-based X-ray microprobes for elucidating the spatial distribution and the speciation of radionuclides in highly heterogeneous waste repository materials will be outlined. A case study on the uptake process of Co in cementitious engineered barrier materials exposed to microbial degradation will be presented. 相似文献
32.
33.
Fan YANG Qinghui HUANG Jianhua LI Xiaomin ZHU 《中国地球化学学报》2006,25(B08):262-262
Dissolved organic matter (DOM) is an important chemical component in natural water. Chromophoric dissolved organic matter (CDOM), a fraction of optical properties, plays art important role in the biogeochemical cycle of nutrients in aquatic environment. People realized that DOM cycle is crucial in the global carbon and nitrogen flux, and also is inherently related to nutrients and trace metal elements. Therefore, CDOM was concerned by scientists in global oceanography and limnology fields. Water samples were collected from three sections (North Channel, South Channel and Zhuyuan) of the Yangtze (Changjiang River) estuary in March 2006 Three-dimensional excitation emission matrix (3-DEEM) fluorescence spectra were analyzed for those filtrates through Whatman GF/F filters. Dissolved organic carbon (DOC) was also measured by TOC analyzer. The tidal variety was also taken into account. The 3-D EEM fluorescence scans suggested the fluorescence characteristics of humic acid (Ex=332-344 nm, Em=439-451 nm) and fulvic acid (Ex=250-254 nm, Em=472-478 nm) were obvious, and the fluorescence group of protein-like and tyrosine (Ex=230 nm, Em=283 nm) was also found. They are mainly composed of CDOM in the Yangtze estuary. Further data analysis, especially the fluorescence index (f 450/500), showed that terrestrial signal was rather strong (1.41-1.65) in the surface water, however, some terrestrial CDOM signals of bottom water showed excursions (1.28-1.39). On the other hand, anthropogenic sign was impressed in the waters of Zhuyuan, which is one of the main drain outlets of Shanghai Metropolis. DOC concentrations ranged from 2.2 mg/L to 3.4 mg/L in Zhuyuan and South Channel, and from 2.0 mg/L to 2.4 mg/L in North Channel. The tide effect played a role in the composition of the CDOM measured by 3-D fluorescence scan technology. 相似文献
34.
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
35.
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
36.
氢化物发生-原子荧光光谱法测定地球化学样品中痕量碲 总被引:4,自引:4,他引:4
采用焙烧富集分离地球化学样品中痕量Te,并用氢化物发生原子荧光光谱法测定。通过实验确定出方法的最佳实验条件,在此条件下获得的检出限为0.005μg/g,线性范围0.025~10μg/g,精密度(RSD,n=8)为5.03%~9.24%。方法已用于国家一级地球化学标准物质中痕量Te的测定,结果与标准值基本相符。 相似文献
37.
理学3080E3型X射线荧光光谱仪维修实例 总被引:2,自引:0,他引:2
介绍理学3080E3型X射线荧光光谱仪样品驱动单元及高压发生器部分的故障现象及维修实例。 相似文献
38.
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
39.
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
40.
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