重庆城区浓雾的基本特征   总被引：13，自引：5，他引：13  

江玉华王强  李子华马力 《气象科技》2004,32(6):450-455

统计分析沙坪坝1951～2002年间发生的浓雾事件，结合2001年12月重庆市雾的外场试验资料，探索重庆市主城区浓雾的基本特征。重庆主城区浓雾随年代演变有减缓趋势；主城区浓雾是自然雾与烟尘等的混合物，河谷及城市效应使雾更浓；城市中出现浓雾的大气边界层特征是在近地面层有逆温及增湿降温现象；高浓度气溶胶的净辐射效应阻碍白天混合层发展，使大气边界层趋于稳定，它是重庆连续几天有雾的原因之一；浓雾具有一定的湿沉降作用，能有限地清洁空气；有浓雾的天气条件下，建议降低污染物的排放总量，以避免严重大气污染事件发生。  相似文献   

SSM/I资料反演大范围地表湿度试验          下载免费PDF全文

谷松岩  张文建邱红 《应用气象学报》2004,15(4):407-416

利用SSM/ I遥感数据, 结合2002年汛期“973”外场观测资料及T106资料, 借助微波辐射传输正演模型, 通过物理反演原理提取SSM/ I低频19 GHz通道像元平均地表微波比辐射率, 然后利用地表微波辐射模型, 估算SSM/ I像元的地表湿度信息。以2002年8月中旬发生在长江流域的暴雨天气过程为例, 将反演得到的地表湿度信息与地面观测到的降水信息进行对比分析, 并与地面的洪涝特征进行对比分析, 得到了与地面降水观测结果较为一致的对比结果。  相似文献   

南京-镇江地区多目标地球化学调查初步成果   总被引：8，自引：1，他引：8  

廖启林  吴新民  金洋 《物探与化探》2004,28(3):257-260

报道了南京—镇江地区开展的多目标地球化学调查工作以来所取得的初步成果,讨论了如何确定土壤中元素的背景值、如何检查评价地球化学异常、如何针对农业地质的需要开展深入研究等问题,并提出了开展调查工作的具体建议。  相似文献   

微波焙烧炉在分析测试中的应用研究     

荣耀 《铀矿地质》2004,20(6):376-379,384

本文详细论述了微波焙烧炉代替马弗炉应用于样品焙烧、熔融、活性炭灰化工作中的实际效果。结果表明：其应用不但可行，而且与马弗炉相比，微波焙烧炉具有更加优越的经济性与环保效果。  相似文献   

内蒙古东部闹牛山铜矿成矿地质背景分析   总被引：4，自引：0，他引：4  

耿文辉  姚金炎 《矿产与地质》2004,18(3):240-244

通过对闹牛山铜矿区与成矿有关的次火山岩岩石化学分析，以及对矿区火山一次火山岩微量元素、稀土元素的分析，结合相关的铅同位素分析，综合分析了该矿床的成矿地质背景。认为：闹牛山铜矿床构造环境属于大陆边缘裂陷带的局部隆起区，成矿火山岩浆为钙碱性，其来源于地壳深部或上地慢，并有上部地壳物质混染。  相似文献   

湘中南二叠系孤峰组硅质岩的成因属性及其地球动力学指示意义   总被引：5，自引：0，他引：5  

付伟  周永章  杨志军  何俊国  张澄博  杨海生 《矿物岩石地球化学通报》2004,23(4):292-300

华南二叠系底部的硅质岩及同一层位对应于华南重要的地幔强活动期和成矿期，有非常重要的动力学指示意义。研究表明，孤峰组剖面的岩性可划分为三段：泥页岩段、厚层状硅质岩段和薄层状硅质岩段。沿剖面自下而上，Al2O3、K2O和TiO2含量逐渐降低，MnO、TFe等组分逐渐升高；稀土元素显示出一定的铈负异常，∑REE偏低，且向上∑REE逐渐减少而HREE／LREE逐渐增高；一些热水沉积诊断性微量元素如As、Sb、Hg等也显示出一定程度的异常。这些特征均表明硅质岩的成岩过程中包含有正常沉积和热水沉积的共同作用，且自下而上热水沉积作用逐渐增强的趋势。这种成岩作用的演化特征，代表了下扬子地台拉张裂陷盆地对晚古生代伸展背景的沉积响应，对于探讨裂谷盆地阶段性发育的动力学特征有一定的指示意义。  相似文献   

无机盐超细粉体制备技术的回顾与展望   总被引：3，自引：0，他引：3       下载免费PDF全文

吴健松  李海民 《盐湖研究》2004,12(3):50-54

评述了制备无机盐超细粉体的传统方法以及一些传统方法的改进 ,对当前几种新技术做了介绍与展望  相似文献   

Absence of extraterrestrial He in Permian-Triassic age sedimentary rocks     

K.A. Farley  P. Ward  S. Mukhopadhyay 《Earth and Planetary Science Letters》2005,240(2):265-275

Helium concentration and isotopic composition were measured in a suite of samples across the Permian-Triassic boundary at Opal Creek, Canada, to determine whether high extraterrestrial helium concentrations are associated with a possible extinction-inducing impact event at this time. No extraterrestrial ³He was detected, implying that neither fullerene-hosted nor IDP-hosted He is present at or near the boundary. This observation is consistent with similar studies of some Permian-Triassic sections, but contrasts sharply with reports of both fullerene- and IDP-hosted extraterrestrial ³He at other sections.Step-heat experiments indicate rapid diffusion of extraterrestrial helium from sediments heated to temperatures above ∼ 70 °C. Given the likelihood of burial and associated heating in Permian-Triassic age rocks, the initially unexpected absence of IDP-hosted ³He likely indicates thermally induced diffusive loss. Indeed one of the key sections (Graphite Peak, Antarctica) from which extraterrestrial ³He has been reported at and near the Permian-Triassic boundary has been sufficiently heated that the reported preservation of extraterrestrial helium, in both IDPs and fullerenes, is inexplicable. Recent contamination provides a plausible explanation for extraterrestrial ³He in these samples.While no extraterrestrial ³He was detected at Opal Creek, there is a sharp increase in nucleogenic ³He very close to or at the Permian-Triassic boundary. This presumably arises from the major lithologic change at this time, from cherts in the Permian to shales and siltstones in the Triassic. Increased nucleogenic ³He is associated with increases in both lithium and organic carbon content into the Triassic. Either the production rate or the retention of this ³He is higher in the shales and siltstones than in the cherts. Care must be taken to eliminate such artifacts before interpreting changes in ³He concentration in terms of fluctuations in the delivery of ³He from space.  相似文献   

Direct Current Plasma Emission Spectrometric Determination of Major, Minor and Trace Elements in Microwave Oven Acid Leachates of Powdered Whole Coal Samples     

Sandro Fadda 《Geostandards and Geoanalytical Research》2005,29(1):143-156

Major concentrations of Al₂O₃, Fe₂O₃, MgO, CaO, Na₂O and K₂O, minor levels of TiO₂, P₂O₅ and thirty petrologically, geochemically and environmentally significant trace elements have been determined in microwave oven acid leachates of whole powdered coal samples by direct current plasma‐atomic emission spectrometry (DCP‐AES). A single sample preparation procedure was suitable for all the determinations with no additional dilution step for major elements solution. Dried samples (0.5 g) were treated in low‐pressure PFA digestion vessels with HF/HCl/HNO₃/HClO₄ acids to quantitatively extract the analytes from the bulk material, while leaving the major part of organic matrix as a residue. The major constituents of geological samples, in particular the easily ionised elements (EIEs) such as alkali and alkaline earths, may complicate the instrumental determinations in DCP‐AES because of differential enhancements of elemental emission intensities and stray light interferences. Taking account of these factors, the coal matrix is considered to have very low major oxide totals as compared to many other common geo‐environmental and related materials (rocks, sediments, soil, ashes etc.). The sample size employed here, while yielding a relatively concentrated solution to cover a wide range of elemental determinations, provided a sample matrix that significantly diminished interferences for DCP measurements. The need for closely matching the unknowns and calibrators was eliminated except for overall acidity and an excess quantity of caesium for EIE buffering. Calibration of the spectrometer was accomplished by simple aqueous single element solutions as high concentration calibrators in addition to a reagent blank as a low concentration calibrator. Two point working curves were established to allow for the maximum concentrations of each element expected in the unknowns. The precision of determinations under routine conditions as well as the reproducibility of the leaching and precision of instrumental measurements have been evaluated. Relative standard deviations (RSD) were of 1–2% for those elements whose concentrations in solid samples were well above the limits of quantification. Method detection limits in the buffered solutions were also evaluated. To evaluate the accuracy of the microwave oven‐DCP method a suite of eight certified coal reference materials of differing rank, were analysed with good agreement with the certified and/or available published data. Results are presented for the uncertified major oxides in the AR series reference materials.  相似文献   

中国东部大陆岩石地球化学图揭示的信息     

迟清华 《地质通报》2005,(Z1)

根据中国东部各省(区、市)区域地质志、1∶50万地质图和中国东部地壳与岩石元素丰度研究成果首次编制的中国东部60种元素的岩石地球化学图,基本反映了与特定岩性有关的区域岩石地球化学元素含量分布特征和与大地构造单元有关的区域地球化学元素含量分布特征,直观表达了中国东部空间地理上元素背景含量的宏观分布与变化,以及不同大地构造单元元素背景含量的变化趋势。这一成果为勘查地球化学、环境地球化学,特别是区域化探扫面水系沉积物资料的定量解释提供了基本依据,为基础地质、大地构造、区域成矿研究提供了重要资料,也为地球化学块体理论及其形成机制的研究提供了强有力的支持。  相似文献