Ecotoxicological monitoring in lakes of Northwestern and Central European Russia situated in specially protected natural areas

An ecotoxicological assessment is given to the state of small lakes in specially protected natural areas in Northwestern and Central European Russia, which suffer from aerotechnogenic acidification. The toxicity of water and bottom sediments is shown to increase with decreasing water pH. The most sensitive characteristics of aquatic organisms in different trophic groups are chosen, allowing the state of lakes to be monitored.     

Optimal instrumentation of structures on flexible base for system identification

A criterion previously developed by Heredia-Zavoni and Esteva for selecting optimal sensor locations is used to analyse the optimal instrumentation of structures on soft soils. The stochastic response of a linear structural system on a flexible base is formulated for use of the criterion. The case of MDOF shear systems on flexible base, with uncertain lateral stiffness and subjected to random earthquake ground motions, is studied. The optimal location of accelerometers, the reduction of prior uncertainty on the lateral stiffness, the effects of the base flexibility, the relative influence of translation and rocking of the base, and the influence of recording noise are assessed and discussed. Copyright © 1999 John Wiley & Sons, Ltd.     

新疆近50a来降水量时空变化及其突变分析

基于新疆53个气象台站1960—2005年逐月降水资料,通过Mann-Kendall非参数趋势检验方法,对新疆近50 a来年降水量和12个月降水量的趋势进行了分析,并计算12个月对年降水量的贡献率,同时通过SequentialMann-Kendall方法分析了27个台站年降水量显著增加趋势发生的时间突变点。结果表明,新疆近50 a来年降水量显著增加,北疆和南疆趋势最为明显;其中冬半年(1、2、11月和12月)这4个月的降水量增加趋势显著,对新疆年降水量的贡献较大;新疆大部分台站年降水量趋势发生突变的时间点在20世纪80年代以后。     

荒漠生态系统C、N、P生态化学计量研究进展

生态化学计量学是通过研究生物有机体主要元素含量及其比值的变化关系,揭示生态系统各组分间元素循环规律的一门学科,生态化学计量也是荒漠生态系统研究的重要内容。因此,综合掌握水分和养分限制环境下C、N、P生态化学计量的关系对揭示荒漠生态系统植物的限制性元素、土壤营养的供给能力、养分的有效性等都具有重要的意义。基于此,回顾和分析了国内外荒漠生态系统C、N、P生态化学计量最新研究和动态,分别从植物、凋落物、土壤、土壤微生物、土壤酶进行较为系统的评述,讨论了植物-土壤-微生物-酶四者的关系,提出了荒漠生态系统C、N、P生态化学计量的未来研究方向,期望为全面理解固沙植被的演变过程、稳定性维持机制及其科学管理提供理论指导。     

The isotopic composition and elemental abundance of lutetium in meteorites and terrestrial samples and the 176Lu cosmochronometer

The isotopic composition of lutetium has been measured in a range of terrestrial and meteoritic materials using solid-source mass spectrometric techniques. The meteoritic and terrestrial isotopic abundances are identical within experimental errors. The absolute ¹⁷⁵Lu/¹⁷⁶Lu ratio as determined in this work is 37.36 ± 0.07 at the 95% confidence level. On the basis of this measurement the atomic weight of lutetium has been calculated to be 174.967 ± 0.002, which is in good agreement with the currently accepted figure of 174.97 ± 0.01.Using the stable isotope dilution technique the abundance of lutetium has been determined in 25 stone, 1 stony-iron and 8 iron meteorites, and in 12 standard rocks, with an accuracy of ±5% at the 95% confidence level. In general, there is good agreement between this work and other published data.The ¹⁷⁶Lu-¹⁷⁶Hf pair has been proposed as an s process nucleocosmochronometer, because of the long half-life of ¹⁷⁶Lu and the unique fact that both are s process isobars. The isotopic and elemental abundances of lutetium as measured in this work have been used with published nuclear data to estimate the mean age of s process nucleosynthesis for this isobaric pair, using the Schramm-Wasserburg formalism. The mean age cannot be accurately determined at the present time because of the lack of 30 keV neutron capture cross-section data for s only process nuclides and an accurate measurement of the branching ratio of ¹⁷⁵Lu + n. However, it is possible to place constraints on the nuclear parameters in this mass region using a reasonable s process chronology based on the decay of ¹⁷⁶Lu.     

Influence of m-cresol purple indicator additions on the pH of seawater samples: correction factors evaluated from a chemical speciation model

The perturbation of the indicator m-cresol purple on the pH in seawater is illustrated in diagrams, representing measurements in 1-cm and 5-cm cells. The diagrams apply to a measured pH interval of 7.4–8.4 using a 2-mM stock solution of m-cresol purple sodium salt dissolved in seawater. The magnitude of the perturbation is described as correction values, i.e., the change in seawater pH caused by the indicator. The diagrams are based on calculations made by using the equilibrium speciation programme, MARINHALT. From these calculations, and least squares fitting methods, pH correction values are described in terms of the pH difference between each seawater sample and the pH of an indicator stock solution. Calculations are performed for a typical high latitude water and a north Pacific deep water. Diagrams are presented for a salinity of 35 and a temperature of 15°C. Responses to salinities between 32 and 36 and temperatures 15–25°C are illustrated as well. A ±0.05 pH difference between a seawater sample and an indicator stock solution gives a correction of less than 0.001 pH unit for a 1-cm cell. For a 5-cm cell, pH differences between the indicator stock solution and a seawater sample as large as ±0.3 cause corrections smaller than ±0.001 pH unit. Calculations demonstrate that the five-fold lower indicator concentration used with 5-cm cells decreases the perturbation effect by approximately a factor of five relative to 1-cm cells.