Occurrence and microbial degradation of phthalate esters in Taiwan river sediments

Concentrations and microbial degradation rates were measured for eight phthalate esters (PAEs) found in 14 surface water and six sediment samples taken from rivers in Taiwan. The tested PAEs were diethyl phthalate (DEP), dipropyl phthalate (DPP), di-n-butyl phthalate (DBP), diphenyl phthalate (DPhP), benzylbutyl phthalate (BBP), dihexyl phthalate (DHP), dicyclohexyl phthalate (DCP), and di-(2-ethylhexyl) phthalate (DEHP). In all samples, concentrations of DEHP and DBP were found to be higher than the other six PAEs. DEHP concentrations in the water and sediment samples ranged from ND to 18.5 μg/l and 0.5 to 23.9 μg/g, respectively; for DBP the concentration ranges were 1.0–13.5 μg/l and 0.3–30.3 μg/g, respectively. Concentrations of DHP, BBP, DCP and DPhP were below detection limits. Under aerobic conditions, average degradation half-lives for DEP, DPP, DBP, DPhP, BBP, DHP, DCP and DEHP were measured as 2.5, 2.8, 2.9, 2.6, 3.1, 9.7, 11.1 and 14.8 days, respectively; under anaerobic conditions, respective average half-lives were measured as 33.6, 25.7, 14.4, 14.6, 19.3, 24.1, 26.4 and 34.7 days. In other words, under aerobic conditions we found that DEP, DPP, DBP, DPhP and BBP were easily degraded, but DEHP was difficult to degrade; under anaerobic conditions, DBP, DPhP and BBP were easily degraded, but DEP and DEHP were difficult to degrade. Aerobic degradation rates were up to 10 times faster than anaerobic degradation rates.     

Optimization of the ionization conditions for the trace analysis of PCDD/PCDF with ion trap MS/MS

Commercial ion trap mass spectrometer provides easy-to-operate MS/MS analysis for the determination of PCDD/PCDF. The limit of quantification is appropriately low (0.2 pg for 23478-P5CDF) because all the stages are performed in the trap and sample losses associated with the ion transportation are minimized. However, if excessive ions are injected into the trap, its electrical fields are distorted and an overall reduction in performance arises. Ionization condition is an important parameter as it affects the amount of the total ions produced. If the amount of interfering compounds are negligible, such as standard solution or cleaned-up sample, lower ionization condition (e.g. electron energy: 30 eV, emission current (EC): 150 μA) is preferable. On the contrary, in case excessive interfering ions are coexisting with PCDD/PCDF, such as crude extract or semi-cleaned-up sample, the ionization condition should be high (e.g. electron energy: 90 eV, EC: 350 μA) for the reproductive quantification.     

Oxidation of acid-volatile sulfide in surface sediments increases the release and toxicity of copper to the benthic amphipod Melita plumulosa

Acid-volatile sulfides (AVS) are an important metal-binding phase in sediments. For sediments that contain an excess of AVS over simultaneously extracted metal (SEM) concentrations, acute or chronic effects should not result from the metals Cd, Cu, Ni, Pb and Zn. While AVS phases may exist in surface sediments, the exposure to dissolved oxygen may oxidize the AVS and release metals to more bioavailable forms. We investigated the role of oxidation of AVS, and specifically copper sulfide phases, in surface sediments, in the toxicity to juveniles of the epibenthic amphipod, Melita plumulosa. Sediments containing known amounts of copper sulfide were prepared either in situ by reacting dissolved copper with AVS that had formed in field sediments or created in sediments within the laboratory, or by addition of synthesised CuS to sediments. Regardless of the form of the copper sulfide, considerable oxidation of AVS occurred during the 10-d tests. Sediments that had a molar excess of AVS compared to SEM at the start of the tests, did not always have an excess at the end of the tests. Consistent with the AVS-SEM model, no toxicity was observed for sediments with an excess of AVS throughout the tests. However, the study highlights the need to carefully consider the changes in AVS concentrations during tests, and that measurements of AVS and SEM concentrations should carefully target the materials to which the organisms are being exposed throughout tests, which in the case of juvenile M. plumulosa is the top few mm of the sediments.     

湖流作用下太湖底泥再悬浮和NH4-N释放规律研究

在矩形水槽中模拟了太湖底泥起动再悬浮规律,分析了湖流流速对太湖底泥再悬浮及NH4-N释放的作用规律.结果显示:当流速小于20 cm/s时,底泥并未发生大量悬浮,水体中浊度及NH4-N浓度变化不大;当流速大于40cm/s时,底泥发生大规模悬浮,水体中浊度和NH4-N浓度显著提高.试验以少量动作为底泥起动的标准,得出太湖底...     

常州市河流重金属污染评价

通过分析2004年常州市河流沉积物重金属的含量,利用地积累指数法,定量评价了河流底泥中重金属污染程度。结果表明:常州市河流底泥已经受到重金属的污染,尤其是Hg污染最为严重。各重金属对常州市河流污染的程度为:Hg>Cd>Cu>Zn>Pb>Cr>As。     

苏州河沉积物中的硅藻及其污染指示作用

阐述了苏州河的北新泾处状沉积物中的硅藻丰度、种类及其数量的变化，优势种属的相对含量的变化。整段沉积物中上、中、下层硅藻的丰度、种类相对很少，苏州河一期污水截流工程建成后，水质有所改善，有利于藻类生长和繁殖，沉积下来的硅藻也增多。结果表明，该柱状沉积物中的硅藻变化能有效地反映苏州河的污染变迁趋势；苏州河的水质污染以前极其严重，近年来有所改善，其主要污染类型为有机污染。     

东海特定海区柱状沉积物中磷的存在形态及其环境指示意义

对国家海洋二所1998年5月调查过程中采自长江口外特定海区的柱状沉积物样品进行了系统的总磷及各形态磷分析。邻近长江口，杭州湾的MESO站位，总磷（TP）、铁结合态磷（Fe-P）和有机磷（OP）增色高于其它站位，表明来自长江、钱塘江水系的污染物已对东海海域的环境造成了一定影响。在垂直方向上，各站位TP、OP和Fe-P的含量自下而上增高，此外，Fe-P和OP由于还原溶解与生物降解等作用，倾向于进入孔隙水，参与海洋磷的再循环。吸附态磷（Ad-P）与钙结合态磷（Ca-P）的含量向上递减，与成岩期自生磷灰石的沉淀，以及磷的吸附-解吸附再平衡有关。     

Heavy metal pollution status in surface sediments of Swan Lake lagoon and Rongcheng Bay in the northern Yellow Sea

The national ‘Shandong Peninsula Blue Economic Zone Development Plan’ compels the further understanding of the distribution and potential risk of metals pollution in the east coast of China, where the rapid economic and urban development have been taken off and metal pollution has become a noticeable problem. Surface sediments collected from the largest swan habitat in Asia, the Swan Lake lagoon and the surrounding coastal area in Rongcheng Bay in northern Yellow Sea, were analyzed for the total metal concentrations and chemical phase partitioning of five heavy metals (Cu, Zn, Pb, Cd, and Cr). Metal contents in the studied region have increased significantly in the past decade. The speciation analyzed by the sequential extraction showed that Zn and Cr were present dominantly in the residual fraction and thus of low bioavailability, while Cd, Pb and Cu were found mostly in the non-residual fraction thus of high potential availability, indicating significant anthropogenic sources. Among the five metals, Cd is the most outstanding pollutant and presents high risk, and half of the surface sediments in the studied region had a 21% probability of toxicity based on the mean Effect Range-Median Quotient. At some stations with comparable total metal contents, remarkably different non-residual fraction portions were determined, pointing out that site-specific risk assessment integrating speciation is crucial for better management practices of coastal sediments.     

吹扫捕集-气相色谱/质谱联用法测定地表水中氯丁二烯

采用吹扫捕集-气相色谱/质谱联用法测定地表水中氯丁二烯。当进样体积为20 mL时,方法在0.100μg/L~50.0μg/L范围内线性良好,检出限为0.05μg/L,标准溶液平行测定的RSD≤3.7%,地表水样加标回收率为91.0%~101%,方法可用于地表水中卤代烃、苯系物等其他21种挥发性有机物的同时测定。     

吹扫捕集- GC/MS法测定水中卤代烃的质量控制指标研究

采用吹扫捕集-气相色谱/质谱联用法,通过实际样品测试及全国多家实验室测定数据统计两种方法,针对水中三氯甲烷、四氯化碳、溴仿、二氯甲烷、1,2-二氯乙烷、1,1-二氯乙烯、三氯乙烯、四氯乙烯等8种卤代烃的平行样测定相对偏差、空白加标回收率及实际样品加标回收率等3个指标,研究了每种卤代烃的质控指标评价标准,提出其平行样测定...