Group Time Delay in the Reflection of P-Polarized Electromagnetic Plane Waves at a Stratigraphic Interface     

Fu-Ping Liu  Rui-Zhong Li  Jin-yao Li  Hui-Guo Chen  Chang-Chun Yang 《Mathematical Geosciences》2008,40(7):813-829

The group time delay (GTD) formulae of quasi-total reflection of inhomogeneous P-polarized electromagnetic waves (P-PEW, whose electric field parallels to the plane of incidence), caused by the Goos–Hänchen effect, is derived by the phase shift of the wave. A numerical example where the frequency equals to 1 GHz is given. The curves of calculating results show that there are three discontinuous points at the critical angle of phase shift vector, the critical angle of attenuation vector and 90^○. When the angle of incidence is equal to one of these three angles, the GTD will become infinite, and the electromagnetic wave will propagate along the interface. The GTD will be very large, when the angle of incidence is close to one of these three angles. The results indicate that there is an important relationship between the two critical angles and the conductivity and permittivity of the two strata, and that the GTD has an important relationship with the angle of incidence. These results can be used to determine the lithology of the strata and to delimit the interfaces of strata more effectively. It is suggested that this research may prove useful in electromagnetic logging analysis and, perhaps, in the design of logging instruments.  相似文献   

矿产预测中成矿信息的提取和强化     

浦志伟  朱裕生 《地质论评》1993,39(6):508-514

成矿信息的提取是矿产预测的重要手段,其方法的有效性直接影响到预测成果的可靠性。在成矿规律研究的基础上,有意识地干预模型的构成,突出与成矿有关的信息;抑制某些成矿意义不明显和属干扰的信息,有目的地使模型向反映成矿信息的方向逼近,提高模型与矿床实际赋存地质环境的吻合程度,均是成矿信息提取和强化的内涵。本文从研究实践中总结了先验约束模型和非先验约束模型的强化方法,在新疆阿勒泰地区的地质－找矿工作中已取得  相似文献   

Particulate content of savanna fire emissions   总被引：9，自引：0，他引：9  

Hélène Cachier  Catherine Liousse  Patrick Buat-Menard  Annie Gaudichet 《Journal of Atmospheric Chemistry》1995,22(1-2):123-148

As part of the FOS-DECAFE experiment at Lamto (Ivory Coast) in January 1991, various aerosol samples were collected at ground level near prescribed fires or under local background conditions, to characterize the emissions of particulate matter from the burning of savanna vegetation. This paper deals with total aerosol (TPM) and carbon measurements. Detailed trace element and polycyclic hydrocarbon data are discussed in other papers presented in this issue.Near the fire plumes, the aerosols from biomass burning are primarily of a carbonaceous nature (C%70% of the aerosol mass) and consist predominantly of submicron particles (more than 90% in mass.) They are characterized by their organic nature (black to total carbon ratio Cb/Ct in the range 3–20%) and their high potassium content (K/Cb0.6). These aerosols undergo aging during their first minutes in the atmosphere causing slight alterations in their size distribution and chemical composition. However, they remain enriched in potassium (K/Cb=0.21) and pyrene, a polycyclic aromatic hydrocarbon, such that both of these species may be used as tracers of savanna burning aerosols. We show that during this period of the year, the background atmosphere experiences severe pollution from both terrigenous sources and regional biomass burning (44% of the aerosol). Daynight variations of the background carbon concentrations suggest that fire ignition and spreading occur primarily during the day. Simultaneous TPM and CO₂ real-time measurements point to a temporal and spatial heterogeneity of the burning so that the ratio of the above background concentrations (TPM/CO₂) varies from 2 to 400 g/kg C. Smoldering processes are intense sources of particles but particulate emissions may also be important during the rapidly spreading heading fires in connection with the generation of heavy brown smoke. We propose emission factor values (EF) for aerosols from the savanna biomass burning aerosols: EF (TPM)=11.4±4.6 and 69±25 g/kg C_{dry plant} and EF(Ct)=7.4±3.4 and 56±16 g C/kg C_{dry plant} for flaming and smoldering processes respectively. In these estimates, the range of uncertainty is mostly due to the intra-fire variability. These values are significantly lower than those reported in the literature for the combustion of other types of vegetation. But due to the large amounts of vegetation biomass being burnt in African savannas, the annual flux of particulate carbon into the atmosphere is estimated to be of the order of 8 Tg C, which rivals particulate carbon emissions from anthropogenic activities in temperate regions.  相似文献   

DDT residue in soil and water in and around the abounded area of DDT manufacturing factory     

Mohammad Rasul Jan Mahmood A Khawaja Jasmin Sha Kashif Gul 《中国地球化学学报》2006,25(B08):182-182

Due to the persistent nature of DDT, a persistent organic pollutant and its adverse environmental and health impacts, the present study was undertaken to examine the residual DDT in and around DDT manufacturing factory in Amman Gharh, Nowshera, NWFP. The factory was established in 1963 and remained in operation till 1994. Composite samples of soil, sediments and water were collected in and around the factory area, nearby DDT stores, main factory drain leading to river and nearby villages. Standard procedures were used for the collection, transportation and storage of samples for analysis. Physical parameters for the collected water samples measured were temperature, pH and conductance. Extraction of each sample for DDT analyses was carried out in triplicates using soxhlet extraction apparatus. The extract was transferred to well washed, clean; dry glass vial, sealed and put in the refrigerator. Gas Chromatograph with electron capture detector and capillary column was used for analysis. DDT in the samples was identified on the basis of their retention time and quantified on the basis of peak areas. It is evident from the analytical data obtained in the present study that both water and soil in and around the factory area are still contaminated with DDT, despite the closure of the factory since the past few years.  相似文献   

Microwave-assisted extraction of organochlorine pesticides from sediments and determination by gas chromatograph with electron capture detection     

Rama Mohan Kurakalva Narasimha Murthy Nyasavajhala Phani Homeshwari Mamidi Venkata Anjaiah Kanukuntla 《中国地球化学学报》2006,25(B08):202-203

A simple and rapid procedure to extract organochlorine pesticides （OCPs） from sediments by means of microwave energy is proposed. Sediment samples were irradiated with microwaves in a closed vessel system while immersed in hexane-acetone （1 ： 1, v/v）. The sample extracts were cleaned up using solid phase extraction with Florisil as adsorbent. Pesticides were eluted with hexane-ethyl acetate （80 ： 20, v/v） and determined by gas chromatographic separation with electron capture detection. Three oven programs were assayed with two different solvent mixtures in order to achieve adequate experimental conditions for the complete extraction of organochlorine pesticides from the matrix. Different variables such as the composition of extraction solvent,  相似文献   

Speciation analysis and significance of ecological geochemistry     

Yaping WANG Chunxue XU Ziyi AN Suming WANG 《中国地球化学学报》2006,25(B08):205-205

Different species of one element have different activities, so it has different effects on environment and human health. To analyze qualitatively and quantitatively the speciation of a special element in sample, which is the important basis for appraising the toxicity and studying the rule of transfer and translation of elements. Since the 1970＇s, the scheme of sequential extraction has already been used at many laboratories both at home and abroard, to get the information about heavy metals＇ activity in polluted soils. Because this method has the experimental nature, many schemes of problem has taken place, the absence of consistency of these sequential extraction have been formed. Thus the complexity of the schemes, the lack of selectivity of reagent, the lack of quality control, the result mainly related to the extraction scheme used, and so on. In the face of these problems, the study of experimental methods of sequential extraction on three different soils, sediment in Dongting Lake, soil in Jiangsu Province and loess in Shanxi Province was made. Reference materials of heavy metal speciation following sequential extraction in soil and sediment had been developed. Nowadays two kinds of sequential extraction methods which are widely used are BCR （three steps） and improved Tessier methods （seven steps）. Based on three steps of BCR, water-soluble speciation and the residual speciation were increased in our research. BCR701 was determined eight times at different laboratories using BCR three steps. The results showed that determined data obtained eight times were identical to the standard value, and it is indicated that this method has good reproducibility. The stability and homogeneity experiments indicated that the preparation of three types of candidates accorded with our requirements. Eight laboratories had afforded the determined values of 12 heavy metal elements （Cu, Pb, Zn, Mn, Co, Ni, Cd, Cr, Mo, As, Sb, Hg, Se et al.） using BCR three steps. Also, these three candidates afforded the determined values by seven steps, and 12 laboratories had participated.  相似文献   

Assessment of mercury mobility and bioavailability by fractionation method in sediments from coastal zone inundated by the 26 December 2004 tsunami in Thailand     

Leonard Boszke  Artur Kowalski  Witold Szczuciński  Grzegorz Rachlewicz  Stanisław Lorenc  Jerzy Siepak 《Environmental Geology》2006,51(4):527-536

The 26 December 2004 tsunami covered significant portion of a coastal zone with a blanket of potentially contaminated sediments. In this report are presented results on mercury concentrations in sediments deposited by the tsunami in a coastal zone of Thailand. Since the total mercury concentrations are insufficient to assess mercury mobility and bioavailability in sediment, its fractionation was applied. Sediments were sampled within 50 days after the event and analyzed by sequential extraction method. The procedure of sequential extraction involved five subsequent stages performed with solutions of chloroform, deionized water, 0.5 M HCl, 0.2 M NaOH, and aqua regia. The mean concentration of total mercury in sediments was 119 ± 50 ng g⁻¹ dry mass (range 66–230). The fractionation revealed that mercury is mainly bound to the least bioavailable sulphides 75 ± 6% (range 62–86), organomercury compounds 14 ± 7% (range 4–26), and humic matter 9 ± 7% (range 1–27). The lowest contributions bring fractions of water-soluble mercury 0.8 ± 1.0% (range 0.1–3.6) and acid soluble mercury 0.9 ± 0.5% (range 0.2–2.1). Although, the total mercury content is similar in a reference sample and in the tsunami sediments, the highly toxic organomercury fraction contribution is higher in the latter. The results were compared with chemical and sedimentological properties of the sediments but no significant correlations were obtained between them.  相似文献   

Distribution of cadmium, chromium, copper, lead and zinc in marine sediments in Hong Kong waters     

S. C. Choi  Onyx W. H. Wai  Thomas W. H. Choi  X. D. Li  C. W. Tsang 《Environmental Geology》2006,51(3):455-461

Partitioning of heavy metals (Cd, Cr, Cu, Pb, Zn) in marine sediments collected from various sites in Hong Kong waters were determined using sequential extraction method. Sediments from Kellette Bank, located in Victoria Harbour, had higher metal concentrations especially Cu and Zn than most other sites. Slightly over 20% of total Cu and Cr existed as readily available forms in Peng Chau and Kellette Bank. At most sampling sites, over 15% of the Cu existed as the exchangeable form indicating that Cu could be readily released into the aqueous phase from sediments. A significantly higher percentage of Pb and Zn was associated with the three non-residual fractions. Hence, there is a greater environmental concern for remobilization of Pb and Zn compared with Cr. The high amount of residual Cd (>50%) and the relatively lower Cd content indicate that little environmental concern is warranted for the remobilization of Cd. Distribution of metals in sediments collected from different depth at Kellette Bank shows that metal concentrations decreased with profile depth. The levels of Pb and Zn associated with the two readily available fractions increased sharply in the surface sediment. These metals represented the pollutants, which were introduced into the area in the mid-eighties through early nineties as a result of rapid economic and industrial development in the territory. As significant portions of these metals were bound to the readily available phases in the surface sediments, metal remobilization could be a concern. An erratum to this article can be found at  相似文献   

环溪河流域土壤氮素含量及影响因素分析     

黄海峰邓良基  胡玉福高雪松 郑小佳 《山地学报》2006,24(B10):98-102

根据67个随机格网样点和分层抽样样点的耕层土壤氮素含量，在ArcGIS9．0平台上运用地统计学等方法研究了环溪河流域土壤氮素含量及其影响因素。结果表明，环溪河流域土壤全氮和碱解氮的平均含量分别为0．60g／kg和53．31mg／kg。研究区土壤全氮含量总体上呈条带状和团块状分布，其低值中心区（〈0．5g／kg）位于团结村不规则三角形区域，并以此为中心向四周增加；高值中心区（〉0．8g／kg）主要位于走马村椭圆状区域。区内土壤碱解氮其高值区（〉75mg／kg）主要分布在深弯村以西，低值区（〈33mg／kg）主要分布于窝窝店村和杨柳村一带。影响区内土壤氮素含量空间分布的因素主要是成土母质、土壤质地、土地利用方式、地貌和坡度。  相似文献   

Retrieval of stratospheric O3 and NO2 vertical profiles using zenith scattered light observations     

G. S. Meena  C. S. Bhosale  D. B. Jadhav 《Journal of Earth System Science》2006,115(3):333-347

Daily zenith scattered light intensity observations were carried out in the morning twilight hours using home-made UV-visible spectrometer over the tropical station Pune (18‡31′, 73‡51′) for the years 2000–2003. These observations are obtained in the spectral range 462–498 nm for the solar zenith angles (SZAs) varying from 87‡ to 91.5‡. An algorithm has been developed to retrieve vertical profiles of ozone (O₃) and nitrogen dioxide (NO₂) from ground-based measurements using the Chahine iteration method. This retrieval method has been checked using measured and recalculated slant column densities (SCDs) and they are found to be well matching. O₃ and NO₂ vertical profiles have been retrieved using a set of their air mass factors (AMFs) and SCDs measured over a range of 87–91.5‡ SZA during the morning. The vertical profiles obtained by this method are compared with Umkehr profiles and ozonesondes and they are found to be in good agreement. The bulk of the column density is found near layer 20–25 km. Daily total column densities (TCDs) of O₃ and NO₂ along with their stratospheric and tropospheric counterparts are derived using their vertical profiles for the period 2000–2003. The total column, stratospheric column and tropospheric column amounts of both trace gases are found to be maximum in summer and minimum in the winter season. Increasing trend is found in column density of NO₂ in stratospheric, tropospheric and surface layers, but no trend is observed in O₃ columns for above layers during the period 2000–2003  相似文献