Organochlorine and Mercury Residues in Young-of-the-Year Spottail Shiners from the Detroit River,Lake St. Clair,and Lake Erie

Young-of-the-year spottail shiners (Notropis hudsonius) were used as biomonitors to determine the spatial distribution (1982/83) and assess trend data for organochlorine and mercury residues. Significantly (p < 0.01) higher PCB residues were found in Detroit River spottail shiners than in collections from southwestern Lake St. Clair and northwestern Lake Erie. The highest PCB residues were found in the west bank collections from Michigan waters (912–2,997ng/g) compared to the mid-stream (96–290 ng/g) and east bank collections (153–316 ng/g). Chlordane residues were found to be elevated in all spottail shiner samples from urbanized areas. Octachlorostyrene and ∑ DDT residues were distributed uniformly within the study area, whereas mercury concentrations were found to be lower in spottail shiners from northwestern Lake Erie than in comparable samples from the Detroit River and southwestern Lake St. Clair. Residues for BHC, heptachlor, aldrin, and chlorinated benzenes were near their detection limits; mirex and chlorinated phenols were not detectable. Recent (1982/83) PCB residue levels in spottail shiners exceeded the IJC aquatic life objective (Great Lakes Water Quality Agreement of 1978) at all the sites sampled, except at Pike Creek in Lake St. Clair. PCB residues in spottail shiners from Pike Creek, Big Creek, and Leamington have declined significantly (p < 0.01) since the mid-seventies. Mercury and chlordane residues have decreased in spottail shiner samples from Leamington, but have remained virtually unchanged at Big Creek and Pike Creek.     

Butyltin Species and Inorganic Tin in Water and Sediment of the Detroit and St. Clair Rivers

Water and sediment samples from 29 locations in the Detroit and St. Clair rivers were analyzed for the highly toxic tri-n-butyltin (Bu₃Sn⁺) species and for the less toxic di-n-butyltin (Bu₂Sn²⁺) and n-butyltin (BuSn³⁺) species and inorganic tin. In general, locations sampled in the St. Clair River were less contaminated with butyltin species than those in the Detroit River. Inorganic tin and BuSn³⁺ were detected in over 90% of all subsurface water samples, while Bu₂Sn²⁺ and Bu₃Sn⁺ were detected in 45 and 28% of the same samples, respectively. The highest concentration ofBu₃Sn⁺ in subsurface water, 5.9 × 10^?10 mol Sn/L, was at the mouth of the Ecorse River, a tributary of the Detroit River. The three butyltin species and inorganic tin were also detected in 23–46% of all sediment samples. The highest concentrations of Bu₃Sn⁺ in sediment were found close to the mouths of the River Rouge, another tributary of the Detroit River, and the Ecorse River, and were 6.2 × I0^–7 and 1.7 × I0^–7 mol Sn/kg dry weight, respectively, for the top 2 cm of sediment.     

Preliminary Assessment of Contaminants in Soft Sediments of the Detroit River

Soft sediments from the Detroit River were analyzed for the USEPA priority pollutants to generally characterize contaminant distribution. Forty-three were detected. Highest heavy metal concentrations were found in the Trenton Channel and immediately downstream of Grosse Ile. They ranged from an area mean (N = 2) of 0.19 mg/kg mercury to 338.7 mg/kg zinc (dry weight). Polynuclear aromatic hydrocarbons ranged from 0.1 mg/kg to 38.8 mg/kg (mean, N = 2) with the highest levels near Grosse Ile. PCBs ranged from 0.015 mg/kg to 1.7 mg/kg (mean, N = 2). Organochlorine pesticides were not detected except for a trace of heptachlor in one sample. Sediment contamination in the Detroit River is widespread with higher concentrations on the U.S. side downstream of the Rouge River and in the Trenton Channel. The significance of these in-place pollutants to biota and as a source to Lake Erie is still unknown.     

Computerised trace method for establishing equations for dimensions and tolerances in design and manufacture

A computerised trace method has been developed for determining the relationships of assembly requirements with design dimensions and tolerances of the components in an assembly, and the relationships of design specifications and machining allowance requirements with manufactured dimensions and tolerances of the component in a process plan. This method traces from the proposed components or planned operations only the dimensions and tolerances that affect the given requirement, and therefore the equations for design or for manufacture can be established simultaneously and accurately. Hence it is possible to establish constraints for the optimisation of dimensions and tolerances for design or for manufacture.     

饲料级磷酸氢钙中氟的几种分析方法比较

本文采用茜素络合酮比色法和氟离子选择电极法对饲料磷酸氢钙进行氟的测定实验对比,得出常用的氟离子选择电极法完全可以代替经典的蒸馏比色法的结论。     

基于高能效及公平性的移动设备定位算法

通过分析校园师生基于GPS的真实活动轨迹,以及何种算法才最适合具有自私性的移动用户展开合作,提出一种高能效及用户公平定位技术.通过采用代理设备合作思想,提出一种集中式最优算法,在保证固定精度界限和设备公平的基础上,实现移动设备GPS时间平均功率最小化.通过控制退避时间和GPS关闭时间,提出一种分布式准最优算法.最后,基于多种拓扑结构进行全面的仿真实验,验证了算法的高能效性和公平性.     

Chemical amplification — A novel approach to ultratrace analysis

The lowest concentration that can be estimated with 100% error in chemical analysis by instrumental technique is referred to as detection limit. It is equal to the ratio of twice the background signal to the magnitude of analytical signal corresponding to a concentration of unity. Detection limit (dl) could be improved if the analytical signal alone could be selectively amplified without affecting the background. It is shown that this could be achieved by chemical amplification. Atomic amplification of two or three orders of magnitude could be obtained by combining two chemical amplifications in series. It is demonstrated that by using heteropoly acid formation as the first amplification reaction and determining molybdenum in the heteropoly acid by catalyticdc polarographic wave, a detection limit for the hetero atom of less than a ppb can be obtained. It is pointed out that the approach of selectively amplifying analytical signals by tandem chemical amplification reactions makes it possible to perform ultratrace analysis (ppb level) with classical instrumental analytical techniques which havedl at ppm level.     

基于电流实部与虚部双向追踪的输电设备利用份额模型及应用

:针对输电设备利用份额的传统定义不能计及有功和无功潮流的耦合作用,基于电流的实部与虚部分量提出输电设备利用份额的新模型及定义。该模型将节点和支路功率转换为电流,通过对电流的实部和虚部分别进行双向追踪,可得到全网用户对输电网的利用份额。该模型不受分配模式的限制,通过恰当处理对地支路,可直接用于联营体模式下输电损耗和成本的完全分摊,文中给出了相关证明。采用“节点分裂”的等效方法和面向元件的分配模式,该方法可实现联营-双边交易共存模式下输电损耗的分摊。以5节点系统为例,对新定义和几种不同定义进行了比较,并对双边交易的增量和边际损耗及本文结果进行了分析。给出的IEEE-30节点算例验证了该方法的有效性。     

石墨炉原子吸收测定化探样品中痕量金的研究

采用以王水分解样品,泡沫塑料富集,硫脲解脱,石墨炉原子吸收分光光度计测定微量金。研究了测定时干燥温度和时间的选择,原子化温度和时间的选择,灰化温度和时间的选择,以及王水体积分数对吸附效果等条件对测定结果的影响。该方法检出限为0.2×10-9,经国家一级分析标准样品验证,结果与标准值相符。