两类双结构矩阵特征值问题的向后误差

讨论2类双结构矩阵特征值问题的向后误差公式和上下界。这2类结构矩阵分别是反对称正交阵和反对称反Hamilton阵。使用的主要技术是基于正交辛相似变换。所得结果可看作Tisseur提出的2个待解决问题的回答。     

C8051F330在地震观测系统中的应用

介绍基于C8051F330单片机的地震观测系统中故障报警子系统的工作原理,并对温度报警设计中的问题进行分析。     

Integration of Sequence Stratigraphic Analysis and 3D Geostatistical Modeling of Pliocene–Pleistocene Delta,F3 Block,Netherlands

This research is focused on the analysis of the sequence stratigraphic units of F3 Block, within a wave-dominated delta of Plio–Pleistocene age. Three wells of F3 block and a 3D seismic data, are utilized in this research. The conventional techniques of 3D seismic interpretation were utilized to mark the 11 surfaces on the seismic section. Integration of seismic sequence stratigraphic interpretation, using well logs, and subsequent 3D geostatistical modeling, using seismic data, aided to evaluat...     

Quantification of Cl,Br and I in Geological Materials by NH4F Digestion: Comparison with Rapid Acid Digestion

The lack of analytical techniques for halogens in geological materials is mainly due to the loss of analytes during sample preparation. This study describes a rapid bulk rock digestion method (NH₄F digestion) for determination of the abundances of Cl, Br and I in geological materials by SF-ICP-MS. During high temperature (200–240 °C) digestion, NH₃ released from the decomposition of molten NH₄F can effectively prevent the loss of halogens released from geological samples. Chlorine, Br and I were not lost during NH₄F digestion at 220 °C for 0.25–6 h. The limits of quantitation for NH₄F digestion were 2.8, 0.018 and 0.003 μg g^-1 Cl, Br and I, respectively. Most results for halogens in geological reference materials by NH₄F digestion were in agreement with their certified values, confirming that the high-performance rapid bulk rock NH₄F digestion has sufficient digestion capability to extract Cl, Br and I from rocks, sediments and soils. In comparison, results obtained following acid digestion showed that HNO₃ + HF digestion could effectively extract Br and I from soil and sediment samples, and that HNO₃ acid digestion is only suitable to use for the determination of Br and I in soil samples.     

珠江三角洲地区土壤F分布及其与地氟病关系初探

笔者结合珠江三角洲地区和中国土壤含F背景,研究了该区土壤F的含量特征、总体和典型区域的分布状况,对土壤类型、成土母质和土地利用类型等影响因素进行了分析,初步探讨了土壤F与地氟病的关系。结果表明,珠江三角洲地区浅层、深层土壤F平均含量分别为510mg/kg和529mg/kg,其中海(陆)相第四纪松散层区的三角洲沉积潜育性水稻土、三角洲盐渍水稻土、基水地的F含量最高。6760km2的浅层土壤F高背景区广泛分布于平原区,东莞、新会、珠海局部呈现污染区;深层土壤F高背景区5504km2,而污染区都集中在邻海的珠海市高栏、三灶两岛。土壤F的富集在沉积物区明显与第四纪海陆、陆海交互相沉积物有关,在基岩区明显和花岗岩类有关,人类影响较强的土壤和水稻土及其盐渍化有利于F富集。区内地氟病分布于从化、增城、东莞郊区、南海、新会和恩平,病区均位于高F的地层岩石区和土壤高F区。土壤F高背景区生长的农作物F含量存在超标,且病区农作物F超标率和超标倍数大于非病区,表明土壤中F的生物有效量比例较高,土壤F已向农产品中迁移和富集,危及到农产品质量。高F的地质环境是造成本区土壤及其农作物F含量高的主要原因,成为地氟病发生的致病因素。     

磷灰石结构通道离子对晶胞参数的影响

磷灰石晶胞参数受其结构中Ca多面体，磷氧四面体及结构通道位置上的类质同角替换的影响，本文探讨了54个磷灰石样吕的晶胞参数与结构通道离子F，OH，Cl相同象替换的影响，本文讨论了54个磷灰石样品的晶胞参数与结构通道离子F，OH，Cl相对含量的关系，发现Cl和取代是影响岩浆型磷灰石晶胞参数的主要因素，每原子／晶胞的Cl使a增大0．121 1（6）nm，c减少0．0633 （3）nm，根据成分与结构的经验关系式，可以验证电子探针对F的分析结果。     

Polychlorierte Dibenzo-p-dioxine, -furane (PCDD/F) und Analoga in Oberflächensedimenten und datierten aquatischen Sedimentkernen

Polychlorinated Dibenzo-p-dioxins, -furans (PCDD/F) and Analogues in Surface Sediments and Dated Aquatic Sediment Cores Aquatic sediments are the final sinks of unintentionally formed PCDD/Fs. Still not known are the conditions of formation of PCDD/Fs in the 8120 years old sediments in Japan and in 350 to 400 years old sediments in the Baltic. Sediments are means of source identification if transformation processes are taken into consideration in view of hydrological conditions. PCDD/Fs have been analysed 30 km from the source in sediments and over a distance of 50 km in benthos indicating a remarkable bioaccumulation potential. Elaborated data of the PCDD/F sediment contamination are missing as well as information on internal diagenetic processes, interactions at the sediment/water interface, and on the aerobic and anaerobic biodegradation and bioavailability of PCDD/Fs in sediments. Quality criteria for sediments and aquatic ecosystems remain to be elaborated.     

黄河矿晶体结构的重新测定及空间群对称的讨论

黄河矿 BaCe(CO₃)₂F(a=0.5072(1)nm,c=3.846(1)nm;V=856.8×10^-3nm³;Z=6)晶体结构的重新测定,采用中心对称空间群 R3m-D_3d⁵,基于337个可观察的单晶 X 射线数据(I>2σ₁)和30个可变参数,R=0.031。原子坐标和均方根振幅(据各向异性位移参数计算,O.013-0.025nm)表明,没有必要降低对称性,即没有必要采用相应的非中心对称空间群或其它次群。黄河矿的结构中,原子形成似层状排列,且垂直于 c 轴;碳酸根通过 Ba 与 Ce 的联结形成三维结构。C(1)O₃,和 C(2)O₃,中的 C 原子偏离三个氧组成的平面,其偏离的距离分别为0.0066(15)nm 和 0.0029(15)nm。