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41.
Rapid industrialization and urbanization along with a growing population are contributing significantly to air pollution in China. Evaluation of long-term aerosol optical depth (AOD) data from models and reanalysis, can greatly promote understanding of spatiotemporal variations in air pollution in China. To do this, AOD (550 nm) values from 2000 to 2014 were obtained from the Coupled Model Inter-comparison Project (CIMP6), the second version of Modern-Era Retrospective analysis for Research, and Applications (MERRA-2), and the Moderate Resolution Imaging Spectroradiometer (MODIS; flying on the Terra satellite) combined Dark Target and Deep Blue (DTB) aerosol product. We used the Terra-MODIS DTB AOD (hereafter MODIS DTB AOD) as a standard to evaluate CMIP6 Ensemble AOD (hereafter CMIP6 AOD) and MERRA-2 reanalysis AOD (hereafter MERRA-2 AOD). Results show better correlations and smaller errors between MERRA-2 and MODIS DTB AOD, than between CMIP6 and MODIS DTB AOD, in most regions of China, at both annual and seasonal scales. However, significant under- and over-estimations in the MERRA-2 and CMIP6 AOD were also observed relative to MODIS DTB AOD. The long-term (2000–2014) MODIS DTB AOD distributions show the highest AOD over the North China Plain (0.71) followed by Central China (0.69), Yangtse River Delta (0.67), Sichuan Basin (0.64), and Pearl River Delta (0.54) regions. The lowest AOD values were recorded over the Tibetan Plateau (0.13 ± 0.01) followed by Qinghai (0.19 ± 0.03) and the Gobi Desert (0.21 ± 0.03). Large amounts of sand and dust particles emitted from natural sources (the Taklamakan and Gobi Deserts) may result in higher AOD in spring compared to summer, autumn, and winter. Trends were also calculated for 2000–2005, for 2006–2010 (when China introduced strict air pollution control policies during the 11th Five Year Plan or FYP), and for 2011–2014 (during the 12th FYP). An increasing trend in MODIS DTB AOD was observed throughout the country during 2000–2014. The uncontrolled industrialization, urbanization, and rapid economic development that mostly occurred from 2000 to 2005 probably contributed to the overall increase in AOD. Finally, China's air pollution control policies helped to reduce AOD in most regions of the country; this was more evident during the 12th FYP period (2011–2014) than during the 11th FYP period (2006–2010). Therefore this study strongly advises the authority to retain or extend these policies in the future for improving air quality.  相似文献   
42.
We present a microphysical model for the surface layer marine and coastal atmospheric aerosols that is based on long-term observations of size distributions for 0.01–100 µm particles. The fundamental feature of the model is a parameterization of amplitudes and widths for aerosol modes of the aerosol size distribution function (ASDF) as functions of fetch and wind speed. The shape of ASDF and its dependence on meteorological parameters, height above sea level (H), fetch (X), wind speed (U) and relative humidity (RH), are investigated. At present, the model covers the ranges H = 0–25 m, U?=?3–18 km s?1, X?≤?120 km and RH?=?40–98%.

The latest version of the Marine Aerosol Extinction Profiles model (MaexPro) is described and applied to the computation and analysis of the spectral profiles of aerosol extinction coefficients α(λ) in the wavelength band λ?=?0.2–12 µm. MaexPro is based on the aforementioned aerosol model assuming spherically shaped aerosol particles and the well-known Mie theory.

The spectral profiles of α(λ) calculated by MaexPro are in good agreement with observational data and the numerical results obtained from the Navy Aerosol Model (NAM) and the Advanced Navy Aerosol Model (ANAM). Moreover, MaexPro was found to be an accurate and reliable tool for investigating the optical properties of atmospheric aerosols.  相似文献   
43.
沙尘气溶胶作为气溶胶的重要类型之一,对全球和区域水分循环以及亚洲季风系统有着重要影响.利用气溶胶自动观测网(AERONET)印度Kanpur和蒙古国Dalanzadgad两个站点数据,采用阈值法提取了沙尘和人为气溶胶信息并进行了对比分析.结果表明,Kanpur站受印度夏季风影响较大,沙尘气溶胶和人为源气溶胶的排放具有叠加效应,远源输送可能是Kanpur站沙尘气溶胶的主要来源.Dalanzadgad站受东亚夏季风影响较小,春季大风带来了大量的沙尘,这可能与大风天气和植被覆盖度低等因素有关,是春季气溶胶光学厚度显著升高的主要影响因素之一,沙尘具有局地起源特征;在其他时段,人为源气溶胶是当地大气气溶胶的主要来源,但总排放量相对较低.此外,Kanpur站所在的恒河流域大气颗粒物绝对含量远远高于Dalanzadgad所在的蒙古国南部地区.在沙尘天气中,两站颗粒物的光学物理特性相似.  相似文献   
44.
中国大气气溶胶辐射特性参数的观测与研究进展   总被引:1,自引:1,他引:0  
长期系统的气溶胶辐射特性观测资料是定量研究气溶胶辐射和气候效应的重要基础.本文综合介绍中国大气气溶胶辐射特性观测与研究现状和成果,重点包括以下内容:地面太阳光度计联网观测气溶胶光学厚度、单次散射反照率、尺度谱;从全波段太阳辐射反演气溶胶光学厚度、单次散射反照率;浊度计和黑碳仪测量地面气溶胶散射系数和吸收系数;地基/星载激光雷达观测气溶胶(后向散射系数)垂直分布;极轨/静止卫星遥感反演气溶胶光学特性.  相似文献   
45.
近40年云南省平均总微雨量占年总雨量比例﹑年平均总微雨日占年总雨日比例均呈下降趋势,并有从北向南逐渐减少的分布规律;近40年云南省年平均能见度也呈下降趋势,其趋势分布同微雨降水趋势分布比较一致;微雨降水的变化同干燥晴天能见度存在正的相关关系,其中云南省东部地区相关显著;而温度与微雨降水存在负相关;云南省气溶胶在一定程度上抑制微雨降水,云南东部气溶胶对微雨的影响比较显著。  相似文献   
46.
华北地区典型污染天大气气溶胶飞机探测个例分析   总被引:5,自引:0,他引:5  
张瑜  银燕  石立新  段英  吴志会 《高原气象》2012,31(5):1432-1438
利用2005年10月17日华北地区一次典型污染天气条件下的飞机探测资料,对石家庄和邯郸气溶胶的微物理特征进行了对比分析,初步讨论了该天气条件下大气气溶胶污染的微观特征和可能原因。结果表明,观测当天石家庄和邯郸地区的气溶胶粒子浓度很高,边界层内气溶胶平均数浓度为103cm-3量级,最高值出现在近地面附近,达到104cm-3量级;边界层以上的数浓度基本都在103cm-3量级,属于空气污染比较严重的一次过程。造成污染的原因是该日晴天风小,大气湍流较弱,不利于污染物扩散和稀释。基于美国国家海洋和大气局(NOAA)后向轨迹模式(HYSPLIT4)对颗粒物进行溯源和追踪分析,发现造成气溶胶浓度较高的气块传输路径主要为西北和偏西路径,境外源主要来自蒙古国,境内源主要来自我国西部,途经甘肃、宁夏、陕西及山西后进入河北。  相似文献   
47.
利用2009年3月-2010年3月大同国家基准气候站20m气象梯度塔的风向、风速、气温、相对湿度的观测资料及PM10质量浓度数据、气溶胶散射系数数据,分析大同地区典型沙尘天气过程近地层气象要素演变特征。结果表明,风速在沙尘暴、扬沙的发生、发展过程中均较大,浮尘较小。气温在沙尘暴期间受冷空气的影响迅速减小,而在扬沙和浮尘天气条件下温度的变化主要取决于长短波辐射的强弱和沙尘气溶胶的辐射强迫。相对湿度在沙尘暴期间基本上呈递增态势,结束后比发生前相对湿度增大,在扬沙和浮尘天气条件下,相对湿度与温度完全呈现出反相关关系,且相对湿度均较小。PM10质量浓度在沙尘暴、扬沙、浮尘天气条件下依次递减。沙尘暴期间气溶胶散射系数明显增大。  相似文献   
48.
张杰  张强  李俊 《气象学报》2010,68(2):207-216
采用MODIS资料和美国发展的MODIS大气温、湿度廓线统计反演算法,估算大气温度、湿度廓线作为初始场,应用101层快速透过率模式(PFAAST)估算了大气透过率,并采用Newton非线性迭代算法反演中国西北荒漠戈壁地区大气温度廓线。结果表明:该方法对边界层高度及以上部分的大气温度反演得比较好,误差基本都在2 K范围内,边界层范围内的温度反演误差较大,反演误差与气溶胶光学厚度增量和地表温度估算误差呈显著正相关关系,与大气水汽混合比的关系较差。文中从敏感性试验和理论分析角度阐述了地表温度和气溶胶光学厚度估算误差对大气温度反演误差的影响,发现不同光谱波段的地表温度权重均随地表温度的增加有不同程度增加,地表温度反演误差增加将增加地表温度权重,提高地表温度估算误差有助于提高地表温度权重的精度;荒漠戈壁地区大气边界层中气溶胶浓度较高,光学厚度较大,使边界层大气透过率降低,进而降低卫星红外遥感波段的地表温度权重和空气温度权重。由于该模式没有很好地考虑边界层中沙尘气溶胶的影响,使卫星反演的大气透过率偏高,以至于高估地表温度权重和大气温度权重,使得反演的表面温度和空气温度偏低。该研究结合太阳光度计获得的光学厚度资料,采用统计方法对气溶胶效应引起的大气透过率误差和表面温度估算误差进行校正,并对物理算法进行本地化改进,实现了边界层温度廓线的反演。  相似文献   
49.
On the formation and growth of atmospheric nanoparticles   总被引:2,自引:0,他引:2  
In this paper we summarize recent experimental, theoretical and observational results on the formation and growth of atmospheric nanoparticles. During the last years significant progress has occurred to explain atmospheric nucleation and initial steps of the growth. Due to climatic and health effects of fine and ultrafine particles the formation and growth of new aerosol particles is of growing interest. The question “How and under which conditions does the formation of new atmospheric aerosol particles take place?” has exercised the minds of scientists since the time of John Aitken, who in the late 1880s built the first apparatus to measure the number of dust and fog particles. However, only during the last 15–20 years has the measurement technology developed to such a level that size distributions of nanometer-size particles and concentrations of gases participating in particle formation can be measured in the atmosphere. Also from a theoretical point of view atmospheric nucleation mechanisms have not been resolved: several mechanisms such as ion-induced (or ion mediated) nucleation, ternary and kinetic (barrier-less) nucleation have been suggested. In the most recent theory, the activation of existing neutral and/or ion clusters has been suggested.  相似文献   
50.
Total suspended particles (TSP), collected during June 2002 to July 2003 in Guangzhou, a typical economically developed city in South China, were analyzed for the organic compound compositions using gas chromatography–mass spectrometry (GC/MS). Over 140 organic compounds were detected in the aerosols and grouped into different classes including n-alkanes, hopanoids, polycyclic aromatic hydrocarbons, alkanols, fatty acids, dicarboxylic acids excluding oxalic acid, polyols/polyacids, lignin products, phytosterols, phthalates and water-soluble sugars. The total amounts of the identified organic compounds including unresolved complex mixture (UCM) ranged from 3112 ng/m3 in spring to 5116 ng/m3 in winter, comprising on seasonal average 2.8% of TSP. Primary organic compounds peaked in winter although there are no heating systems burning fuels in Guangzhou. The highest saccharide levels occurred in fall due to agricultural activities. This study demonstrated that utilization of fossil fuels, biomass burning, soil resuspension and plastic/refuse burning are the major contributors to the identified organic compounds in the urban atmosphere of South China.  相似文献   
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