外差激光雷达测量水体布里渊散射可行性研究

该文分析外差激光雷达测量水体布里渊散射的可行性。借助测量水体布里渊散射的频移 ,可得到水体声速或温度。文中利用两条 12 7I2 吸收线锁定激光输出频率 ,产生稳定的频差约为7.5 GHz发射激光和激光本振。通过对 12 7I2 吸收线稳定度、激光频率稳定度、系统信噪比和反演精度的分析和计算机模拟 ,得出水体深度 2 5 m以内水体布里渊散射频移的测量误差可以控制在2 .5 MHz以内 ,达到水中声速 0 .6 m/ s或温度 0 .1℃的测量精度。     

温度、体重和摄食水平对花尾胡椒鲷幼鱼粪便比能值及吸收率的影响

鱼类没有消化的食物通过粪便而排出体外.没有消化的食物、黏液、消化道脱落细胞、代谢酶以及细菌等就组成了鱼类的粪便.排粪后所保留的食物能可以通过吸收率来估算,其计算式为:A=C-FC/C×100%,式中A(吸收率)以百分数表示;C(摄食量)等于摄入的食物质量乘以食物比能值;F(粪便排出量)等于排出的粪便质量乘以粪便比能值.吸收率在营养学上又称为消化率.粪便比能值的测定在计算吸收率时是非常必要的,但在以往对鱼类吸收率的研究[1～6]中,由于粪便收集的困难及粪便的样品量通常很少,均没有对不同条件下鱼类所排出粪便的比能值进行单独的测定.     

等离子体质谱法测定玄武岩中微量元素三种样品预处理方法的比较

在测定玄武岩的微量元素时,为了保证得到的微量元素结果反映源区特征,需经预处理去除玄武岩的孔洞中充填的碳酸盐等物质。选取雷州半岛新生代玄武岩三个样品,每一个样品用三种预处理方法进行预处理,等离子体质谱法测定其中的微量元素。分析结果表明,用稀硝酸浸泡样品,会导致玄武岩中大多数微量元素严重丢失,得到的数据失真;而用稀盐酸浸泡去除碳酸盐的方法基本不改变玄武岩中微量元素的含量。     

Influence analysis of gaseous absorption on “HY-1A” CZI data processing Simulation and correction for Rayleigh scattering

Besides ozone, oxygen and water vapour should be considered for their absorptive effects on ＂HY--1A＂ CZI data processing. First ,gaseous transmittances under various conditions are computed and analyzed for the band settings of this sensor. Second, transmittances under six standard atmospheres are approximated as functions of zenith angle, the water vapour transmittance is approximated as a function of water vapour content and zenith angle, and the ozone transmittance is approximated as a function of ozone content and zenith angle. Finally, taking Rayleigh scattering as an example, the influence of ignoring gaseous absorption when calculating TOA reflectance is analyzed, and the effect of applying the presented transmittance approximations to gaseous absorption correction for Rayleigh scattering in ＂HY--1A＂ CZI data processing is evaluated.     

利用AutoPrep技术抑制型电导离子色谱法检测土壤中碘

利用AutoPrep自动样品前处理技术，对土壤燃烧吸收液进行在线预浓缩，抑制型电导进行检测，建立了一种全新思路的检测土壤样品中碘的方法。选择亲水性非常强的氢氧化物选择性IonPac AS16阴离子交换色谱柱，淋洗液发生装置在线产生KOH进行等梯度淋洗，抑制型电导检测。结果表明，对于土壤燃烧吸收液中碘离子的测定，方法检出限（S／N=3）可达1．2μg/L，线性相关系数为0．9998，方法精密度（RSD，n=7）为1．161％～4．566％，回收率在90．6％～100．8％。采用AutoPrep电导检测和脉冲安培检测离子色谱法测定不同土壤样品中的碘，两种方法的检测结果基本一致。方法在提供了稳定的系统空白的同时，还具备自动化程度高、操作简单、重现性好、灵敏度高、系统稳定、节约时间、成本低廉和对环境友好等多方面特点，适合于大批量土壤普查中碘的分析。     

高压密闭消解-电感耦合等离子体光谱和质谱联合测定海洋地质样品中52种元素

An improved analytical method to determine the content of 52 major, minor and trace elements in marine geological samples, using a HF-HCl-HNO_3 acid system with a high-pressure closed digestion method(HPCD), is studied by an inductively coupled plasma optical emission spectrometry(ICP-OES) and an inductively coupled plasma mass spectrometry(ICP-MS). The operating parameters of the instruments are optimized, and the optimal analytical parameters are determined. The influences of optical spectrum and mass spectrum interferences, digestion methods and acid systems on the analytical results are investigated. The optimal spectral lines and isotopes are chosen, and internal standard element of rhodium is selected to compensate for matrix effects and analytical signals drifting. Compared with the methods of an electric heating plate digestion and a microwave digestion, a high-pressure closed digestion method is optimized with less acid, complete digestion,less damage for digestion process. The marine geological samples are dissolved completely by a HF-HCl-HNO_3 system, the relative error(RE) for the analytical results are all less than 6.0%. The method detection limits are 2–40μg/g by the ICP-OES, and 6–80 ng/g by ICP-MS. The methods are used to determine the marine sediment reference materials(GBW07309, GBW07311, GBW07313), rock reference materials(GBW07103, GBW07104,GBW07105), and cobalt-rich crust reference materials(GBW07337, GBW07338, GBW07339), the obtained analytical results are in agreement with the certified values, and both of the relative standard deviation(RSD) and the relative error(RE) are less than 6.0%. The analytical method meets the requirements for determining 52 elements contents of bulk marine geological samples.     

有效吸收和传递波浪能的锚泊系统的设计制作

将传统定位浮标加以改进,可以形成一种能有效吸收和传递波浪能的锚泊系统。此系统的最上端是漂浮着的海面浮标,海面浮标下端连着锚泊钢缆,锚泊钢缆下端到海底之间又依次连有张紧锤、储链和重物锚块。锚泊系统中的海面浮标随波浪同步上下起伏,从而带动与其连在一起的由张紧锤绷直的锚泊钢缆上下振动,于是海面浮标吸收波浪能并由引导缆向下传递。20 m长的储链可以保证整个装置在涨潮、退潮的极限水深情况下,仍旧可以有效地传递海表面波浪能;合适的重物锚块可以起到为整个系统定位的功能。最后给出了一个实际应用波浪能的例子。设计制作的锚泊系统可以有效吸收和传递波浪能,为波浪能的利用提供了一种行之有效的方法。     

Holocene calcrete crust deposits on the moraine of Batura Glacier, northern Pakistan

Abstract   Calcretes can be observed on the surface of old moraines around Batura Glacier in the upper Hunza Valley, Karakoram Mountains, Pakistan. They develop as a calcareous crust cementing small gravels under boulders. In order to understand the genesis of the calcrete crust, a variety of methods were employed: (i) study of mineralogy and geochemistry of a calcrete crust precipitated on the lateral moraine using X-ray diffractometer and electron probe microanalysis; (ii) analysis of solute chemistry of surface water and ice bodies around the Batura Glacier; and (iii) accelerator mass spectrometry ¹⁴C dating of the crust itself. The results indicate that the calcrete crust has definite laminated layers composed of a fine-grain and compact calcite layer, and a mineral fragment layer. The chemical composition of the calcite layer is approximately 60% CaO and 1% MgO. The mineral fragment layer consists of rounded grain materials up to 0.2 mm in diameter. It shows a graded bedding structure with fine grains of quartz, albite and muscovite. Meanwhile, as the Paleozoic Pasu limestone is distributed around the terminal of Batura Glacier, Ca cations dissolve in the melt water of the glacier. Accordingly, the calcrete crust is precipitated by decreases in CO₂ partial pressure from glacier ice and evaporation of the melt water, including high concentration of Ca²⁺ at ephemeral streams and small ponds stagnating between the moraine and glacial ice. On the basis of the AMS ¹⁴C age, the calcrete is considered to have formed approximately 8200 calibrated years bp under the Batura glacial stage.     

X射线荧光光谱分析方法的共享

探索了在同一类型X射线荧光光谱仪器之间分析方法共享的可能性。基于量值归一的原理,使用标准化样品建立了两台仪器之间测量数据的可比性,使一台X射线荧光光谱仪建立的分析方法,能够简单转移到其他同一类型的X射线荧光光谱仪上使用,可以获得同样的分析精确度和准确度,从而实现分析方法的共享。实验数据表明,建立的方法简单、实用,能够节约分析方法建立过程中的人力、物力和资源,又能够更好地发挥科学仪器的作用,促进分析方法的标准化和网络化。     

UTEVA树脂分离纯化珊瑚中铀、钍的改进研究

珊瑚是记录海洋环境变化信息的载体之一,测定其U/Ca比值可重建海水温度或测定Th/U同位素比值可计算年龄重建海平面高度等。准确测定珊瑚中U、Th含量及同位素比值是提取所记载的海洋环境变化信息的前提,其难点在于高Ca基体分离和痕量U、Th富集纯化。基于此,本研究拟采用UTEVA树脂改进了一步富集分离珊瑚中U、Th的前处理方法,并联合高分辨电感耦合等离子体质谱仪测定U、Th含量。结果证明：上样介质HNO₃浓度由3 mol/L降至2 mol/L不影响U、Th的吸附效率,用2 mL Milli-Q水可将U完全洗脱,U、Th的全流程空白值（mean±1σ, n =12）分别为（1.32±0.65） pg、（2.05±0.63）pg,显著降低了U的全流程空白值。测定了3个海南滨珊瑚中U含量（mean±1σ,n=6）,分别为（3.46±0.02 ）μg/g、（2.67±0.05）μg/g、（2.15±0.07）μg/g,Th含量（mean±1σ,n=6）分别为（10.12±0.24）ng/g、（4.82±0.10）ng/g、（5.62±0.12）ng/g,测定精度均在3.3%以内,U、Th加标回收率分别为97.9%～100.9%、97.3%～99.7%,方法准确度高,精密度好。本研究可为测定珊瑚等碳酸盐类样品中U、Th含量及其同位素提供准确、简便和快速的样品前处理方法。