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91.
The analysis of sand samples by x-ray fluorescent spectroscopy (XRF) gives the ratio of the geochemical elements to construct the sand samples. The x-ray analysis therefore shows the geochemical characteristics of sand in the sampled area. In this study, sand is sampled on coasts and rivers of the Noto Peninsula to determine the geochemical elements and to show the geological characteristics that occur, especially iron and calcium. The experiments show the effect of rivers and Kotogahama beach on iron and calcium, respectively. Applying the method of ratio matching to the measured data of the geochemical elements, the direction of movement of sand on the coast is determined by considering the correlation matrix and the ratio of geochemical elements between sand samples at two locations. The predominant longshore direction movement of sand offshore in the study area is from south to north. Sand in rivers is not directly transported to adjacent beaches; however, offshore sand is transported to beaches. The estimated direction of movement of sand longshore near coastal structures agrees with observations. The proposed method to predict the direction of movement of sand gives the correct one in comparison with the observed data in rivers.  相似文献   
92.
本文阐述平流层气溶胶的光学常数在不同温度下取值时,用Mie散射理论对不同浓度的平流层气溶胶红外波段的辐射特性进行的计算和分析。分析结果表明:在卫星遥感中,由温度引起的平流层气溶胶光学常数的变化对某些红外波段的平流层气溶胶辐射特性的影响是不容忽视的。  相似文献   
93.
Individual aerosol particles collected in the Negev desert in Israel during a summer and winter campaign in 1996–1997 were analysed by scanning electron microscopy with energy-dispersive X-ray analysis. Hierarchical cluster analysis was performed to interpret the data on the basis of particle diameter and composition. Eleven particle classes (groups) provided clues on sources and/or particle formation. The summer samples were enriched in sulphates and mineral dusts; the winter samples contained more sea salts, aged sea salts, and industrial particles. The fine size fraction below 1 m diameter was enriched in secondary particles and showed evidence of atmospheric processing. The secondary sulphate particles were mainly attributed to long-range transport. A regional conversion from calcite to calcium sulphate occurred during summer. Industrial particles originating from local pollution appeared during winter.  相似文献   
94.
A simple mathematical model is described, which reproduces the major features of sand waves' appearance and growth and in particular predicts their migration speed. The model is based on the linear stability analysis of the flat configuration of the sea bottom subject to tidal currents. Attention is focused on the prediction of the complex growth rate that bottom perturbations undergo because of both oscillatory fluid motions and residual currents. While the real part r of controls the amplification or decay of the amplitude of the bedforms, the imaginary part i is related to their migration speed. Previous works on the migration of the sand waves (Németh etal. 2002) consider a forcing tide made up by the M2 constituent (oscillatory period equal to 12 h) plus the residual current Z0 and predict always a downcurrent migration of the bedforms. However, field cases exist of upcurrent-migrating sand waves (downcurrent/upcurrent-migrating sand waves mean bedforms moving in the direction of the steady residual tidal current or in the opposite direction, respectively). The inclusion of a tide constituent characterized by a period of 6 h (M4) is the main novelty of the present work, which allows for the prediction of the migration of sand waves against the residual current Z0. Indeed, the M4 tide constituent, as does also the residual current Z0, breaks the symmetry of the problem forced only by the M2 tide constituent, and induces sand-wave migration. The model proposed by Besio etal. (2003a) forms the basis for the present analysis. Previous works on the subject (Gerkema 2000; Hulscher 1996a,b; Komarova and Hulscher 2000) are thus improved by using a new solution procedure (Besio etal. 2003a) which allows for a more accurate evaluation of the growth rate for arbitrary values of the parameter r, which is the ratio between the horizontal tidal excursion and the perturbation wavelength. Responsible Editor: Jens Kappenberg  相似文献   
95.
Gas phase ozonolysis of -pinene was performedin a 570 l static reactor at 730 Torr and 296 K insynthetic air and the products were analysed by acombination of gas phase FTIR spectroscopy, HPLC andIC analyses of gas phase and aerosol samples,respectively. The reaction mechanism was investigatedby adding HCHO, HCOOH and H2O as Criegeeintermediate scavenger and cyclohexane as OH radicalscavenger. Main identified products (yields inparentheses) in the presence of cyclohexane as OHradical scavenger were HCHO (0.65 ± 0.04),nopinone (0.16 ± 0.04), 3-hydroxy-nopinone (0.15± 0.05), CO2 (0.20 ± 0.04), CO (0.030± 0.002), HCOOH (0.020 ± 0.002), the secondaryozonide of -pinene (0.16 ± 0.05), andcis-pinic acid (0.02 ± 0.01). The decompositionof the primary ozonide was found to yieldpredominantly the excited C9-Criegee intermediateand HCHO (0.84 ± 0.04) and to a minor extent theexcited CH2OO intermediate and nopinone (0.16± 0.04). Roughly 40% of the excitedC9-Criegee intermediate becomes stabilised andcould be shown to react with HCHO, HCOOH and H2O. The atmospherically important reaction of thestabilised C9-Criegee intermediate with H2Owas found to result in a nopinone increase of (0.35± 0.05) and in the formation of H2O2(0.24 ± 0.03). Based on the observed products,the unimolecular decomposition/isomerisationchannels of the C9-Criegee intermediate arediscussed in terms of the hydroperoxide and esterchannels. Subsequent reactions of the nopinonylradical, formed in the hydroperoxide channel, lead tomajor products like 3-hydroxy-nopinone but also tominor products like cis-pinic acid. A mechanismfor the formation of this dicarboxylic acid isproposed and its possible role in aerosol formationprocesses discussed.  相似文献   
96.
碱尘暴期间松嫩平原西部碱尘气溶胶的主要元素质量浓度排序为Na、Al、Fe、Ca、Mg、K、Ti、Ba、Zn,与当地盐碱化土壤的元素组成吻合,而与沙尘、城市气溶胶的元素组成有差别。风力对碱尘气溶胶元素组成有明显的影响,当风速在8.0~17.1 m/s时,元素组成的质量浓度排序为Na、Ca、Al、Fe、Mg、K、Ba、Ti、Zn。Na元素质量浓度的激增是碱尘暴元素组分的一大特征,明显富集元素为Na和B;相对于当地背景大气气溶胶的富集情况,Zn、Cu、Ba、B的富集因子值在碱尘暴期间明显降低;在各种天气情况下,B、Cu均具有较高的富集因子。碱尘中Ti元素的富集因子值均小于1,而Ca、Fe、K、Mg、Mn、Sr、V的富集因子值为1~4。两个采样点的Ca、Na、Al、Fe、Mg、Ti、Zn的富集因子近似,表明该区碱尘的主要元素具有特定的一致性;而B、Ba、Cu、V的富集因子相差较大,可以作为区分不同碱尘源的标志性元素。  相似文献   
97.
生物质燃烧颗粒物有机示踪化合物的测定和应用   总被引:2,自引:0,他引:2  
使用气相色谱-质谱法对2002年7月-2003年7月的北京市大气粗、细颗粒物样品中的左旋葡聚糖等糖类化合物进行了测定。结果表明,左旋葡聚糖主要存在于细颗粒中,可以作为示踪化合物来研究生物质燃烧现象。生物质燃烧对北京市大气颗粒物有较重要的贡献。对应于12%-40%的PM2.5有机碳和10%-33%的PM10有机碳。北京市在2002年10月和11月受到明显的生物质燃烧的影响,可能由于农田秸杆焚烧和秋季落叶焚烧。2003年5月7日颗粒物样品受到直线距离约为1000km以外的内蒙古自治区呼伦贝尔市大兴安岭林区森林大火烟雾的影响。生物质燃烧事件具有突发性,可以长距离传输;生物质作为农村生物燃料的使用其燃烧排放具有经常性和持久性的特征。  相似文献   
98.
云模式中气溶胶物理过程参数化方案研究概述   总被引:2,自引:1,他引:2  
刘校辰  刘奇俊 《气象》2006,32(6):3-12
介绍了大气气溶胶的浓度、气溶胶的谱形等物理性质对云的微物理过程造成的影响以及目前云模式中常用到的一些气溶胶物理过程的体积水、分档等参数化方案,并评述了这些参数化方案各自的特点。提出了在设计气溶胶物理过程参数化方案时需要注意和有待解决的几个问题,建议在设计气溶胶-云相互作用的模式时,要根据不同的研究目的选择合适的参数化方案。  相似文献   
99.
国内外气溶胶观测网络发展进展及相关科学计划   总被引:16,自引:6,他引:16  
气溶胶是气候变化研究中的一个极大的不确定性因素,国内外在此方面开展了大量的观测和科学研究。本文首先对当前全球两大气溶胶观测网络,世界气象组织(WMO)的全球大气观测计划(GAW)和气溶胶自动观测网(AERONET)的组织、规模、设备、数据和气溶胶网络的规范作了介绍,并对近年来国际上的重大气溶胶科学计划的目标、实验方法、步骤作了介绍,说明观测网络的重要性。在此基础上对中国气溶胶观测网络的地位做了分析,并指出其在正在开展的中国气溶胶科学研究中的重要性。  相似文献   
100.
With the size-resolved aerosol mass and ion composition data obtained at Lin'an regional atmospheric pollution monitoring station in July 2003, the size distributions of aerosol mass and ionic components, and the correlations between major ion pairs were analyzed. The primary results indicate that in the period of in-situ measurement, the aerosols are mainly composed of fine particles. The mass of aerosols with size less than 2.1μm accounts for 66% of the total mass of all size ranges, in which about 50% of the mass is contributed by the particles with size less than 0.65μm. Similar to the size distributions of aerosol mass, the water-soluble ions are mainly concentrated in the size range of <0.65μm, accounting for about 77% of the sum of analyzed ions, and the ions within the range of <2.1μm reach 88%. The sulfate, ammonium, and potassium are the dominant ionic components in fine particles (particle size less than 2.1μm). Ion correlation analysis suggests that the sulfates in fine particles are mostly in the compounds of (NH4)2SO4, Na2SO4, and K2SO4, but for submicron particles the sulfates are mainly in the form of (NH4)2SO4.  相似文献   
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