Community analysis in stream biomonitoring: what we measure and what we don't

Diatom assemblages from 83 epilithic samples taken from the Mesta River, Bulgaria, were regressed against three sets of predictor variables, i.e. environmental, spatial, and temporal. Redundancy analysis (RDA) of species and environmental data explained 36% of the diatom variance and extracted several important gradients of species distribution, associated with a downstream increase in nutrient levels, pH, temperature, and organic pollution. The inclusion of spatial and temporal variables in the RDA model captured additional 24% of the diatom variance and revealed three more gradients, a spatial gradient represented by higher order polynomial terms of latitude and longitude, and two temporal gradients of annual and seasonal variation. Partial RDAs demonstrated that the unique contribution of each predictor set to the explained diatom variance was the highest in the spatial dataset (16%), followed by the environmental (9%), and the temporal (7%) datasets. The remaining 28% of the variance was explained by the covariance of the predictor sets. This suggests that in biomonitoring of single stream basins, the cheap and simple account of space and time would explain most of the variance in assemblage composition obviating the necessity of expensive and time-consuming environmental assessments. The nature of the underlying environmental mechanisms can be easily inferred from the diatom composition itself.     

聚苯乙烯基硫代磺酸钾树脂的合成及其与卤代烃的反应

由聚苯乙烯基磺酰氯树脂与硫化氢钾反应制备聚苯乙烯基硫代磺酸钾树脂（Ｉ），树脂Ｉ与亲电的卤代烃反应，生成聚苯乙烯基硫代磺酸酯树脂（Ⅱ），树脂Ⅱ经过乙硫醇处理，使卤代烃结构部分以不对称二硫醚的形式游离下来，用ＧＣ／ＭＳ对其结构进行鉴定。从不对称二硫醚的结构可推导出原卤代烃的结构，所制备的聚苯乙烯基硫代磺酸钾树脂的转化效率为１．１１ｍｍｏｌ·ｇ＾－１。     

水中一氯胺和二氯胺的紫外连续流动测定

本文研究了二氯胺与溴化钾的反应及其产物。采用微孔渗透膜分离－紫外分光测定系统，测定水溶液中的一氯胺与二氯胺。本法的线性范围为２×１０＾－５ｍｏｌ·ｌ＾－１－１×＾－２ｍｏｌ·ｌ＾－１，标准偏差在２×１０＾－４ｍｏｌ·ｌ＾－１时为４．３％。     

Applying a new method for direct collection, volume quantification and determination of N2 emission from water

The emission of N₂ is important to remove excess N from lakes, ponds, and wetlands. To investigate the gas emission from water, Gao et al. (2013) developed a new method using a bubble trap device to collect gas samples from waters. However, the determination accuracy of sampling volume and gas component concentration was still debatable. In this study, the method was optimized for in situ sampling, accurate volume measurement and direct injection to a gas chromatograph for the analysis of N₂ and other gases. By the optimized new method, the recovery rate for N₂ was 100.28% on average; the mean coefficient of determination (R²) was 0.9997; the limit of detection was 0.02%. We further assessed the effects of the new method, bottle full of water, vs. vacuum bag and vacuum vial methods, on variations of N₂ concentration as influenced by sample storage times of 1, 2, 3, 5, and 7 days at constant temperature of 15°C, using indices of averaged relative peak area (%) in comparison with the averaged relative peak area of each method at 0 day. The indices of the bottle full of water method were the lowest (99.5%-108.5%) compared to the indices of vacuum bag and vacuum vial methods (119%-217%). Meanwhile, the gas chromatograph determination of other gas components (O₂, CH₄, and N₂O) was also accurate. The new method was an alternative way to investigate N₂ released from various kinds of aquatic ecosystems.     

Rapid and simple spectrophotometric determination of persulfate in water by microwave assisted decolorization of Methylene Blue

A rapid and simple method for determination of persulfate in aqueous solution was developed. The method is based on the rapid reaction of persulfate with Methylene Blue(MB) via domestic microwave activation, which can promote the activation of persulfate and decolorize MB quickly. The depletion of MB at 644 nm(the maximum absorption wavelength of MB) is in proportion to the increasing concentration of persulfate in aqueous solution. Linear calibration curve was obtained in the range 0–1.5 mmol/L, with a limit of detection of 0.0028 mmol/L. The reaction time is rapid(within 60 sec), which is much shorter than that used for conventional methods. Compared with existing analytical methods, it need not any additives, especially colorful Fe2+, and need not any pretreatment for samples, such as p H adjustment.     

荧光法快速测定浮游植物以及应用于梅梁湖预警监测可行性探讨

YSI 6600-V2多功能水质自动监测仪采用荧光原理快速测定水体中浮游植物蓝绿藻的密度,梅梁湖夏季水华高发期时,湖体中的浮游植物几乎全部是蓝绿藻。传统的浮游植物监测前处理方面就需要24~48 h,最终要数天后才有镜检结果,导致浮游植物数据滞后,不能很好的应用到预警监测中。通过比对相关性验证,保证荧光法数据的可信度,提高工作效率,为预警监测提供有力的支持。     

扩散电化学法现场测定高湿度烟气中低浓度二氧化硫能力的 研究

根据目前定电位电解法出现的问题,对扩散电化学法测定固定污染源高湿度烟气中低浓度二氧化硫的能力展开研究。结果显示,扩散电化学法测定值与参比值保持较好的一致性,说明该方法不受固定污染源烟气浓度、湿度以及负压等因素的影响,对高湿烟气中低浓度二氧化硫具备较强测定能力,非常适合该状况下SO₂的现场测定。但是方法也受传感器制约,适用范围受到限制。     

氧化淀粉等稀糊淀粉的流度及测定

介绍了淀粉工业中氧化淀粉等稀糊淀粉的流度测定及其意义。     

树状河流突发污染事故源强确定方法研究

源强确定在突发污染事故的预警与应急过程中极为重要。本文针对树状河流的特性，将污染源搜索和源强反算的方法结合起来构建了树状河流突发污染事故源强确定的一般方法，并利于假设的突发污染事故情形对方法就行了评估。结果表明，监测数据的误差对计算结果的影响很大，源强的计算结果相比事故的地点与发生时间更为敏感。