太湖水体吸收系数与散射系数的特征研究   总被引：19，自引：2，他引：19       下载免费PDF全文

俞宏  蔡启铭  吴敬禄 《水科学进展》2003,14(1):46-49

湖泊水体光学特性是进行湖泊水体光学及水体光学遥感研究的基础。计算了太湖冬、夏季水体的吸收系数和散射系数,并在分析水体吸收特性的基础上对水体的光学类型进行了分类。结果表明:冬季太湖水体的光学类型属PY型(悬浮粒和黄质共同作用型),即水体的吸收特性受悬浮质和黄质的共同作用,而夏季则属CPY型(浮游藻类、悬浮粒和黄质共同作用型),即水体的吸收特性受悬浮质、黄质和浮游藻类三者的共同作用;不论冬季还是夏季,非色素悬浮粒是影响太湖水体散射特性的主要因子。  相似文献   

重油凝胶色谱制备样品中痕量镍的分析研究          下载免费PDF全文

朱玉霞许世科  陆婉珍 《岩矿测试》2003,22(2):129-133

研究表明微波密闭消解法对重油凝肢色谱制各样品的前处理，不造成易挥发有机金属化合物的损失，对样品无污染。采用消解前定容，配合石墨炉二次进样富集样品，可以测定样品中低至10^—9级的镍。方法应用于镍在渣油中随相对分子质量分布分析中，标准样品对照数据吻合好，相对标准偏差(RSD，n＝11)为8％。  相似文献   

机载激光测深中的波浪改正技术   总被引：3，自引：0，他引：3  

黄谟涛  翟国君  欧阳永忠  陆秀平 《武汉大学学报(信息科学版)》2003,28(4):389-392

基于我国新研制的机载激光测深系统基本配置，提出了3种可供选择的波浪改正计算方案(也称为深度值归算方案)，具体分析了3种方案的适用条件和应用范围，并从理论上对3种改正模型的计算精度进行了估算。  相似文献   

从激光扫描数据中进行建筑物特征提取研究   总被引：42，自引：4，他引：42  

李必军  方志祥  任娟 《武汉大学学报(信息科学版)》2003,28(1):65-70

提出了一套基于建筑物几何特征的信息挖掘方案，并具体介绍了研究中采用的一些原理、方法与实用算法，从而可以直接从激光扫描数据中提取建筑物的平面外轮廓信息。利用本方案对车载激光扫描系统获取的城市建筑物试验数据进行了具体的处理，并给出了三维建模和可视化表达结果。  相似文献   

Formation of Concentric Rings Around Sources     

B. P. Harlamov 《Mathematical Geology》2003,35(4):431-449

Zones of increased concentration formed by a solvent flowing from a source are considered. A matehmatical model for forming such zones is proposed. It takes into account that such a zone is composed of a set of independent particles. Hence the distribution of a substance around the source can be explained by movement of an individual particle. In the model this movement is a continuous semi-Markov process with terminal stopping at some random point in space. Parameters of the process depend on the velocity field of the flow. Forward and backward partial differential equations for the distribution density of a random stopping point of the process are derived. The forward equation is investigated for the centrally symmetric case. Solutions of the equation demonstrate either a maximum or a local minimum at the source location. In the latter case a concentric ring around the source is formed. If different substances vary in their absorption rates, they can form separable concentration zones as a family of concentric rings.  相似文献   

Preliminary Results from a New 157 nm Laser Ablation ICP-MS Instrument: New Opportunities in the Analysis of Solid Samples     

Philippe Telouk  Estelle F. Rose-Koga  Francis Albarede 《Geostandards and Geoanalytical Research》2003,27(1):5-11

Preliminary results are given from an excimer 157 nm laser ablation multiple-collector inductively coupled plasma-mass spectrometer (LA-MC-ICP-MS), used for the isotopic measurements of solid materials. Elements of geological interest with different volatilities such as Pb and U (e.g. zircon geochronology) and Cu and Zn (as examples of geochemical/biochemical tracers) were analysed. The range of ablation rates of 20-150 nm s^-1 enabled us to ablate the sample down to a depth of 45 μm for a 50 μm diameter pit. The Cu and Zn isotopic measurements gave values that were very stable with, on average, a 0.01 % standard error, comparable with that achieved in liquid mode measurements.  相似文献   

Laser Ablation ICP-MS Analysis of Geological Materials Prepared as Lithium Borate Glasses   总被引：9，自引：0，他引：9  

Stephen M. Eggins 《Geostandards and Geoanalytical Research》2003,27(2):147-162

A simple, rapid and precise method is described for determining trace elements by laser ablation (LA)-ICP-MS analysis in bulk geological materials that have been prepared as lithium borate glasses following standard procedures for XRF analysis. This approach reliably achieves complete sample digestion and provides for complementary XRF and LA-ICP-MS analysis of a full suite of major and trace elements from a single sample preparation. Highly precise analysis is enabled by rastering an ArF excimer laser (λ= 193nm) across fused samples to deliver a constant sample yield to the mass spectrometer without inter-element fractionation effects during each analysis. Capabilities of the method are demonstrated by determination of twenty five trace elements (Sc, Ti, V, Ga, Rb, Sr, Y, Zr, Nb, Cs, Ba, REE, Hf, Ta, Pb, Th and U) in a diverse range of geological reference materials that includes peridotites, basalts, granites, metamorphic rocks and sediments. More than 90% of determinations are indistinguishable from published reference values at the 95% confidence level. Systematic bias greater than 5% is observed for only a handful of elements (Zr, Nb and U) and may be attributed in part to inaccurate calibration values used for the NIST SRM 612 glass in the case of Zr and Nb. Detection limits for several elements, most notably La, are compromised at ultra-trace levels by impurities in the lithium borate flux but can be corrected for by subtracting appropriate procedural blanks. Reliable Pb analysis has proved problematic due to variable degrees of contamination introduced during sample polishing prior to analysis and from Pt-crucibles previously used to fuse Pb-rich samples. Scope exists for extending the method to include internal standard element/isotope spiking, particularly where integrated XRF analysis is not available to characterise major and trace elements in the fused lithium borate glasses prior to LA-ICP-MS analysis.  相似文献   

A Reappraisal of Rb, Y, Zr, Pb and Th Values in Geochemical Reference Material BHVO-1     

William J. Chazey III  Clive R. Neal  Jinesh C. Jain  William S. Kinman 《Geostandards and Geoanalytical Research》2003,27(2):181-192

The geochemical reference material BHVO-1 was analysed by a variety of techniques over a six year period. These techniques included inductively coupled plasma-mass spectrometry and atomic emission spectroscopy (ICP-MS and ICP-AES, respectively), laser ablation ICP-MS and spark source mass spectroscopy. Inconsistencies between the published consensus values reported by Gladney and Roelandts (1988, Geostandards Newsletter) and the results of our study are noted for Rb, Y, Zr, Pb and Th. The values reported here for Rb, Y, Zr and Pb are generally lower, while Th is higher than the consensus value. This is not an analytical artefact unique to the University of Notre Dame ICP-MS facility, as most of the BHVO-1 analyses reported over the last ten to twenty years are in agreement with our results. We propose new consensus values for each of these elements as follows: Rb = 9.3 ± 0.2 μg g-1 (compared to 11 ± 2 μg g-1), Y = 24.4 ± 1.3 μg g-1 (compared to 27.6 ± 1.7 μg g-1), Zr = 172 ± 10 μg g-1 (compared to 179 ± 21 μg g-1), Pb = 2.2 ± 0.2 μg g-1 (compared to 2.6 ± 0.9 μg g-1) and Th = 1.22 ± 0.02 μg g-1 (compared to 1.08 ± 0.15 μg g-1).  相似文献   

MTMD对建筑结构多模态控制的减震分析   总被引：5，自引：1，他引：5  

涂文戈  邹银生 《地震工程与工程振动》2003,23(5):174-179

本文研究了MTMD对建筑结构多模态减震控制。将主结构简化为多自由度模型，MTMD对结构的反力与地震荷载共同作为结构的荷载输入进行分析；基于主结构多模态耦合进行推导分析，阐述了MTMD与结构之间的相互作用关系，提出MTMD的复惯性质量。提出MTMD的控制类型是加速度相关型的无源被动控制。从频域传递函数，白噪声、宽带和窄带地震激励下的结构相对位移和绝对加速度谱密度，以及El-centro地震波作用下结构的地震响应三个方面，分析了MTMD对顶部带有结构附属物的结构的控制效果。并且给出TMD的控制效果加以比较验证。算例说明MTMD多模态控制对结构的相对位移和绝对加速度均有较好的控制效果，并且优于TMD控制效果。  相似文献   

Photochemistry of N2O4 Adsorbed on Ice Surfaces at 193 nm     

Akio Susa  Seiichiro Koda 《Journal of Atmospheric Chemistry》2003,45(2):197-217

A multi-layer deposited ice film was prepared through water vapor deposition on a Ni plate in a vacuum chamber at 90 K, and was used as it was or after annealing at 140 K. NO₂ was adsorbed as N₂O₄ approximately 90 K on the ice film prepared as above, and irradiated by 193 nm excimer laser light. The time-of-flight (TOF) spectra of the desorbed species, i.e., NO₂, NO, O₂ and O, were measured by a quadrupole mass spectrometer. The photochemical process obeyed an one-photon process. The relative yields of the products and their TOF spectra were dependent on the preparation condition of the ice film and also varied with the continuation of the laser irradiation. From the ice film annealed at 140 K, NO₂, NO and O₂ were desorbed with an approximate ratio of 1:1:0.01. From the non-annealed film, the relative yield of NO₂ was much smaller than that of NO. The TOF spectrum of NO from the non-annealed ice film consisted of distinctly different two components corresponding to the 1700 and 100 K translational temperature, respectively. The fast component was lost when additional ice was deposited on the adsorbed N₂O₄. NO was supposed to be a predissociation product from the electronically excited NO₂ prepared through the photodissociation of N₂O₄.  相似文献