云南个旧南部地区元素地球化学特征

在野外调研和大量样品采集分析的基础上， 运用数学地质中对应分析和因子分析两种方法对样品和变量进行分类划分和成因解释。首先，将样品和元素进行综合计算，按第一、二因子轴作出样品－元素因子平面图，在图上划分四个象限，按象限进行分类，探讨其样品－元素分类规律。其次，按象限计算因子载荷矩阵，分析各因子轴所代表的元素共生组成规律和成矿期次。根据上述研究认为第一因子轴（F1）所代表的Sn、Cu、Pb、Cu、Zn、Au、Ag等元素为主成矿元素组合和主成矿期次，而其它因子轴所代表的Mo、W、Bi、Be等元素为次成矿元素组合和次成矿期次。成矿作用是在区域构造应力驱动力的作用下，与花岗岩侵入有关。成矿溶液除来自深源以外，还与周围基性岩体（脉）和围岩密切相关，矿液实质是一种混合矿浆，在上升运移过程中，充填在有利的构造部位和有利 的地层层位中形成矿体。     

Trace Elements Analysis of Geological Samples by Laser Ablation Inductively Coupled Plasma Mass Spectrometry

ＩＮＴＲＯＤＵＣＴＩＯＮＬａｓｅｒａｂｌａｔｉｏｎｉｎｄｕｃｔｉｖｅｌｙｃｏｕｐｌｅｄｐｌａｓｍａｍａｓｓｓｐｅｃｔｒｏｍｅ ｔｒｙｉｓａｎｉｎｃｒｅａｓｉｎｇｌｙｄｅｖｅｌｏｐｅｄａｎａｌｙｔｉｃａｌｔｅｃｈｎｉｑｕｅｆｏｒｓｏｌｉｄｓａｍｐｌｅａｎａｌｙｓｉｓ.ＬＡ ＩＣＰ ＭＳｏｆｆｅｒｓａｔｔｒａｃｔｉｖｅｃｈａｒａｃｔｅｒｉｓｔｉｃｓｏｆｈｉｇｈｓｅｎｓｉｔｉｖｉｔｙ ,ｌｏｗｄｅｔｅｃｔｉｏｎｌｉｍｉｔｓ,ｍｉｎｉｍａｌｓａｍｐｌｅｐｒｅｐａｒａ ｔｉｏｎ ,ｌｅｓｓｏｘｉｄｅｓｉｎｔｅｒｆｅ…     

PAN－PVAβ修正新光度法测定地表水中的微量锌

本文研究了ｚｎ（Ⅱ）与ＰＡＮ和ＰＶＡ在ＮＨ＿４Ｃｌ－ＮＨ＿４ＯＨ缓冲介质中的显色反应，提出在５２０ｎｍ处用β修正新光度法测定微量锌。该法可准确消除剩余显色剂的干扰，分析精密度、灵敏度和线性范围均比单波长高，修正吸光度（Ａ＿ｓ）与Ｚｎ（Ⅱ）浓度在０－１．４μｇ／ｍｌ符合比耳定律，检出限０．０２μｇ／ｍｌ，样品加标回收率／％９３－９６，方法适合环境水样中锌的测定。     

井地直流电法三维数值模拟中若干问题研究

讨论了地下垂直线源分段计算和场叠加的方法,并实现了在套管上供直流电的三维数值模拟。讨论了大型容量矩阵的压缩存储方式,采用数组和结构体相结合的方法实现容量矩阵的一维链表式压缩存储。在求解超大型稀疏线形方程组时引入不完全Cholesky分解稳定化的双共轭梯度算法(ICBG),通过与均匀半空间垂直线源解析解的对比,证明了该算法是准确可靠的。     

高硒环境样品中硒的形态分析方法

在恩施富硒碳质岩和土壤样品中硒矿物学研究的基础上,提出了硒连续化学提取的改进方案。化学操作上定义为7个连续步骤:水溶态(MQ水提取)、可交换态(0.1 mol/L的K2HPO4 KH2PO4,pH=7.0)、有机结合态(0.1 mol/L NaOH)、元素态(1 mol/L Na2SO3溶液)、酸溶性提取态(15%CH3CO2H溶液)、硫化物/硒化物态(1 mol/L CrCl2 HCl溶液)和残渣态硒(HNO3 HF H2O2混合消化液)。使用HG-AFS法检测了各结合态中的硒形态和总硒,上述流程提取硒加和与总硒间显著一致,平均回收率为99.2%,符合平行样品间变异系数低于10%的精度要求。该方法简单易行,能够准确地揭示富硒地质样品中硒的形态信息。     

Evaluation of Simultaneous Analyte Leaching/Vapour Phase Introduction for Direct Osmium Isotope Ratio Measurements in Solid Samples by Double-Focusing Sector Field ICP-MS

The analytical performance of a method for Os isotope ratio measurement by double‐focusing, sector field ICP‐MS (ICP‐SFMS) was evaluated. The method is based on several optimised, concurrent processes: Os extraction from samples in hot concentrated nitric acid; separation of Os from the digest solution by the formation of volatile osmium tetroxide accelerated by continuous hydrogen peroxide addition; transport of analyte vapour by an oxygen flow into the ICP; and isotopic determination by ICP‐SFMS. Due to the very efficient utilisation of analyte (approaching 0.5‰), Os isotope ratio measurement could be performed at low pg levels. Combined with an ability to process sample sizes up to 2 g (up to 50 g if the organic matrix of biological or botanical samples is eliminated by ashing), materials with Os concentrations in the low, or even sub pg g^?1 range could be determined by this method. Given that two complete digestion/distillation systems were available for interchangeable use, throughputs of up to fifteen samples per 8 hour shift could be achieved. The method precision, evaluated as the long‐term reproducibility of ¹⁸⁷ Os/¹⁸⁸Os ratio measurements in a commercial Os reference sample containing 0.5 ng Os, was 0.16% relative standard deviation (RSD, 1s). The method has been applied to perform replicate ¹⁸⁷ Os/¹⁸⁸ Os ratio measurements on a suite of fifty reference materials of various origins and matrix compositions, with Os concentrations varying from < 0.1 pg g^?1 to > 100 ng g^?1, yielding an average precision of 3% RSD. Though none of the materials tested are certified for Os content or Os isotope composition, comparison of the obtained data with published Os isotope information for similar sample types revealed close agreement between the two. The method can also be used for the simultaneous, semi‐quantitative determination of Os concentrations.     

基于对应分析的训练样本的选择

本文提出一种基于对应分析的训练样本的选择方法。它从训练样本中自动地选择有代表性的典型训练样本,使得在自动分类中充分利用所采集的样本信息,以便得到满意的分类结果。通过实验与分析证明,该方法是可行的,它明显优于人工随机选择训练样本的方式。与基于Q型因子分析的训练样本选择方法相比,可以更快地得到较少的典型样本,满意的分类精度。     

Estimation from incomplete data files based on magnitude-frequency relation for earthquakes

The problem of incorporating the available seismological information provided by the major events of the historical catalog with those for the short period of instrumental data is investigated. Assuming that the frequency-magnitude law of Gutenberg and Richter is valid for both periods, an estimation procedure for the main parameter of this law and the rate of earthquake occurrence for historical period is presented. Application of the proposed method is demonstrated, using both real and simulated data. An extension to allow for variable quality of complete data with different magnitude values is also included.     

应用实时定量PCR技术检测秦皇岛近岸海域褐潮原因种——抑食金球藻(Aureococcus anophagefferens)

Aureococcus anophagefferens, a small pelagophyte algae, has caused brown tide blooms in coastal waters of Qinhuangdao in recent years, presenting significant negative impacts on the shellfish mariculture industry. Under standard light microscopy, it is visually indistinguishable from other small algae in field samples due to its extremely small size. In this study, quantitative polymerase chain reaction(q PCR) based on 18 S r DNA sequences was developed and used to detect and enumerate A. anophagefferens. A linear regression(R2 = 0.91) was generated based on cycle thresholds value(Ct) versus known concentrations of A. anophagefferens. Twenty-two field samples collected in coastal waters of Qinhuangdao were subjected to DNA extraction and then analyzed using q PCR. Results showed that A. anophagefferens had a wide distribution in coastal waters along Qinhuangdao. Elevated A. anophagefferens abundance, category 3 brown tide blooms(200 000 cells/m L) occurred at Dongshan Beach and Tiger-stone Beach in August in 2013. In shellfish mariculture areas along coastal waters of Qinhuangdao, 4 stations had category 3 blooms, and 6 stations had category 2 blooms(35 000–200 000 cells/m L) in August and all stations had category 1 blooms(0 to ≤35 000 cells/m L) in October. Quantitative PCR allows for detection of A. anophagefferens cells at low levels in filed samples, which is essential to effective management and prediction of brown tide blooms.