Radio Sources and Scintillation

A review is given of the interplay between studies of compact radio sources and the scattering and scintillations that occur as the signals travel through the irregular refractive index of the interstellar and interplanetary plasmas. This revised version was published online in July 2006 with corrections to the Cover Date.     

Chemical and boron-isotope variations in tourmalines from an S-type granite and its source rocks: the Erongo granite and tourmalinites in the Damara Belt,Namibia

Tourmaline is widespread in metapelites and pegmatites from the Neoproterozoic Damara Belt, which form the basement and potential source rocks of the Cretaceous Erongo granite. This study traces the B-isotope variations in tourmalines from the basement, from the Erongo granite and from its hydrothermal stage. Tourmalines from the basement are alkali-deficient schorl-dravites, with B-isotope ratios typical for continental crust (δ¹¹B average −8.4‰ ± 1.4, n = 11; one sample at −13‰, n = 2). Virtually all tourmaline in the Erongo granite occurs in distinctive tourmaline-quartz orbicules. This “main-stage” tourmaline is alkali-deficient schorl (20–30% X-site vacancy, Fe/(Fe + Mg) 0.8–1), with uniform B-isotope compositions (δ¹¹B −8.7‰ ± 1.5, n = 49) that are indistinguishable from the basement average, suggesting that boron was derived from anatexis of the local basement rocks with no significant shift in isotopic composition. Secondary, hydrothermal tourmaline in the granite has a bimodal B-isotope distribution with one peak at about −9‰, like the main-stage tourmaline, and a second at −2‰. We propose that the tourmaline-rich orbicules formed late in the crystallization history from an immiscible Na–B–Fe-rich hydrous melt. The massive precipitation of orbicular tourmaline nearly exhausted the melt in boron and the shift of δ¹¹B to −2‰ in secondary tourmaline can be explained by Rayleigh fractionation after about 90% B-depletion in the residual fluid. Electronic supplementary material The online version of this article (doi:) contains supplementary material, which is available to authorized users.     

海水中234Th的超低水平液闪谱仪测定

本文提出了利用超低水平液闪谱仪测定海水中234Th的方法.海水经氢氧化铁吸附共沉淀富集后,接着用阴离子交换和TBP/煤油萃取进行Th同位素的分离与纯化.对一系列测定条件进行了详细的研究,提出了测定海水中234Th的适宜程序,即在含有234Th和产额示踪剂230Th的纯化后的5mol/dm3HNO3溶液中加入TBP/煤油进行萃取,然后用0.1mol/dm3HNO3反萃取,后者是先用契伦柯夫计数法测量234Th(通过234mPa),后加入闪烁液Hisafe 3用α/β模式测量α放射体230Th.对于α和β放射体液闪谱仪的计数效率分别为100%和55.7%±2.7%.234Th的化学回收率和总探测效率分别为70%～80%和30%～45%.该法测定海水中的234Th快速、简便和高效.     

A comparative study on the contents of vitamins in the natural and the cultured prawn

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液体中光声信号吸收衰减的研究

研究水的声吸收所引起的光声脉冲幅度的变化。脉冲声波由激光通过光击穿机制产生。文中给出了光声脉冲峰值声压与传播距离和声吸收系数之间的理论关系式。实验测量结果和理论曲线所描述的变化规律相符合。     

围隔实验中水柱颗粒物色素的动态研究

用高效液相色谱法(HPLC)研究了围隔实验过程中水柱颗粒物主要色素的组成及动态变化,并就滤食性鱼类鲢对水体主要色素代谢的影响进行了讨论。结果表明:水柱中的主要色素有叶绿素a、异黄素、岩藻黄素、黄体素、玉米黄素和蓝藻叶黄素等,未放鱼的围隔中实验后期各种色素含量均降低到最低水平,有鱼的围隔中鱼类密度越高则色素含量降低越多。未放鱼的围隔中叶绿素a代谢产物———脱植基叶绿素a、脱镁叶绿素a、脱镁叶绿酸a与叶绿素a的比值均大于其它围隔,有鱼的围隔中鱼类密度大的这几个比值也比较大。     

Counting chronology and climate records with about 1000 annual layers of a Holocene stalagmite from the Water Cave in Liaoning Province, China

One active stalagmite from the Water Cave in Liaoning Province contains growth layers of three sizes. Based on thermal ionization mass spectrometry 230Th dating, we found that middle size layers are annual layers, with each middle layer consisting of one narrow dark layer and a wide bright layer. The small layers within middle layers are sub-annual layers and the large layers are multi-year layers. Based on the layer-counting method, we established a high-resolution time scale for layer thickness. Our results reveal two dramatic century-scale climate cycles over the past 1000 years in this region.     

溶液结构的X射线衍射研究──4.用粉末衍射仪精确测定溶液结构的新方法

本文叙述了用θ—2θ型X射线衍射仪精确测定电解质溶液结构的新的实验技术，设计制作了具有恒温功能的超厚液体样品池，并建立了样品池窗口强度的校正方法。建立在Johansson和Yamaguchi工作基础上，发展了液体X射线衍射数据处理和结构参数精细化的计算机程序，获得了非常令人满意的实验结果。由θ－2θ型X射线衍射仪精确测定的径向分布函数与θ－θ型衍射自由表面散射比较，表明DRF分辩率有所提高。     

新版建筑工程建筑面积计算规范应用探讨

GB/T 50353-2013建筑工程建筑面积计算规范于2014年7月1日开始实施,该规范是在总结原有规范基础上进行修订的,目前,新规范实施已经一年多了,依据新规范审批的建设工程陆续进入验收阶段,因此,在建筑面积测量中如何正确用好新规范显得尤为重要。本文就新规范的技术要点进行分析,以便于技术人员和管理人员正确使用新规范。     

高效液相色谱-电感耦合等离子体质谱联用检测土壤中的无机硒形态

土壤样品中亚硒酸盐Se(Ⅳ)和硒酸盐Se(Ⅵ)的形态分析中,提取剂的选择和检测方法是技术的关键。以往的提取剂容易导致硒形态发生转变或无法同时提取Se(Ⅳ)和Se(Ⅵ),常用的氢化物发生原子荧光光谱法无法直接测定Se(Ⅵ),而是通过差减法得出Se(Ⅵ)含量。本文对比了不同提取剂的提取能力,确定使用0. 1 mol/L氢氧化钠溶液作为提取剂,在55℃超声萃取土壤样品30 min,提取液经高效液相色谱分离,电感耦合等离子体质谱检测,建立了土壤中Se(Ⅳ)和Se(Ⅵ)的形态分析方法。采用Hamilton PRP X-100色谱柱,以6 mmol/L柠檬酸为流动相,pH=5. 5,在8 min内可完全分离Se(Ⅳ)和Se(Ⅵ),两者的检出限分别为0. 15μg/L、0. 16μg/L,线性相关系数(r~2)均大于0. 999。以土壤为基体进行加标回收试验,Se(Ⅳ)和Se(Ⅵ)的回收率在84. 2%～95. 8%之间,相对标准偏差为1. 4%～5. 3%(n=6)。该方法简单快速,具有良好的精密度和准确度,适用于土壤中无机硒的形态分析。