制革废水处理系统各级出水的生态毒性评价

采用生态毒理学常用的大型溞（Daphnia magna）和活性污泥（activated sludge）作为试验系统,对制革废水处理系统各个环节出水进行毒性试验,以评价其处理效果。按照OECD标准试验方法,选取本实验室繁殖的大型溞（溞龄小于24 h）,和采自以处理生活污水为主的污水处理厂活性污泥,分别使用重铬酸钾和3,5-二氯酚作为参比物验证大型溞和活性污泥的毒性敏感性。以大型溞活动抑制和活性污泥呼吸抑制作为毒性终点,利用48 h静态试验和3 h曝气试验分别评价水样对于大型溞活动和活性污泥呼吸作用的急性毒性效应。统计各试验组大型溞的活动情况和活性污泥的呼吸速率,分别将其与空白对照组进行比较,计算大型溞的活动抑制率和活性污泥的呼吸抑制率,采用Bliss法统计制革废水处理系统各个环节出水对大型溞和活性污泥的半数抑制浓度（EC50）。结果表明：制革废水依次经过厌氧脱硫反应器、脱色厌氧反应器、微曝气反应器和厌氧氨氧化反应器的生物处理系统处理,其出水对大型溞和活性污泥的急性毒性已大为降低。进水、厌氧脱硫反应器出水、脱色厌氧反应器出水、微曝气反应器出水和厌氧氨氧化反应器出水对大型溞活动抑制试验的48 h-EC50分别为41.3%、32.2%、48.0%、91.2%和无抑制作用;活性污泥呼吸抑制试验3 h-EC50则分别为178.2%、101.5%、689.7%、184.6%和无抑制作用。总体上毒性呈现逐渐降低的趋势,而且大型溞比活性污泥更为灵敏。大型溞和活性污泥的生态毒性结果与化学分析的结果相互补充,可为制革废水处理提供预警和效果评价提供科学依据。     

焦化废水处理试验系统出水的生物毒性变化

焦化废水是一种典型的难降解工业废水,组分复杂,生物毒性高,大多采用生物处理联合物化深度处理的工艺,以满足炼焦化学工业的污染排放标准,但其排水安全性仍然令人担忧。为研究工艺排水安全性,选择发光细菌青海弧菌Q67、稀有鮈鲫(Gobiocypris rasus)血红细胞、活性污泥微生物群落为测试生物,研究了焦化废水及各处理阶段出水的急性毒性和遗传毒性变化,进而识别影响生物毒性的水质因子。焦化废水经过序批式生物膜反应器处理后,出水急性毒性比进水下降71%,遗传毒性下降为90%以上的轻度以下损伤,显示生物强化处理对焦化废水生物毒性有良好的去除作用。生物处理出水再经过深度处理后,则表现出不同的毒性变化:活性炭吸附法对生物急性毒性的消除最佳,但遗传毒性较生物处理出水有所升高;臭氧氧化法不仅水质改善效率差,且最终出水的生物急性毒性与遗传毒性均升高;臭氧催化氧化法对水中残留有机物去除效率较高,但也造成出水急性毒性与遗传毒性的升高。各水样对青海弧菌Q67的急性毒性与有机物、氮等水质指标表现出较强相关性,而遗传毒性与水质指标之间的相关性不显著。研究结果可为评价和改进处理工艺、保障水体生态安全提供参考。     

长江三角洲地区城市污泥的综合生物毒性研究

运用发光细菌法对我国长江三角洲地区16个城市中54个污泥样品的综合急性生物毒性进行了测定，并以毒性较为稳定的HgCl2作为参比毒物，以发光细菌抑光率、相当标准毒物HgCl2质量浓度及百分数等级比较法毒性划分标准评价城市污泥的毒性。结果表明，供试的不需稀释测定毒性的城市污泥中，有13个是剧毒的，占样品总数30．95％；需稀释测定毒性的城市污泥中，毒性等级为Ⅰ级的8个，占样品总数66．67％。长江三角洲地区城市污泥大部分有较高的综合急性生物毒性，这与含多种高量的有毒重金属有关。城市污泥对发光细菌毒性的大小与城市污泥来源、污水处理工艺及污泥类型等因素有关。上海地区的污泥毒性大于江苏和浙江地区；42个毒性较小的污泥中，大部分氧化沟处理的城市污泥的毒性要大于A^2／O（厌氧-缺氧／好氧）处理的，12个毒性较大的污泥中处理工艺多为活性污泥处理与A^2／O处理；大部分以生活污水和混流污水为主的城市污泥毒性要高于以工业污水为主的城市污泥。     

广州市某A2/O工艺城镇污水处理厂出水对大型溞的生殖毒性作用

城镇污水处理厂废水中存在大量生物毒性物质,但该废水对动物的生殖能力影响研究还十分缺乏。利用大型溞暴露实验,检测广州市某采用A~2/O工艺的城镇污水处理厂出水的急性毒性和生殖毒性。48 h急性毒性实验表明,所有水样均未表现出急性毒性效应。慢性生殖毒性(14 d)测试结果表明:(1)从进水到缺氧池出水均能显著提高第一胎产溞数量;(2)进水和沉砂池出水显著增加受试期总产溞数量;(3)从厌氧池到出水工艺段受试溞的第一胎产溞时间均推后;(4)好氧池出水的毒性显著降低,但仍然对大型溞具有生殖毒性。研究表明,好氧池(A~2/O)工艺能够显著去除具有大型溞生殖毒性的物质,但污水处理厂废水的生殖毒性仍需要引起关注。     

某石化废水的综合毒性评价及其处理工艺对毒性的削减规律研究

利用生物毒性测试对环境中的污染物进行生态风险评价,是目前风险评价中的研究热点。本研究以明亮发光杆菌(Photobacterium phosphoreum)、斜生栅藻(Scenedesmus obliquus)和大型溞(Daphina magna)为受试生物,对某石化厂废水的处理流程中5个主要单元出水的急性毒性进行了测试,分析了其急性毒性与理化指标间的相关性;同时,为了解不同处理单元毒性去除效果及主要毒性来源,结合毒性鉴别评价(toxicity identification evaluation,TIE)技术对各阶段出水的毒性削减及其主要致毒物质类别进行了分析。毒性测试结果表明,该废水处理厂对石化废水的毒性去除效果比较显著,其中进水对明亮发光杆菌、斜生栅藻和大型溞分别表现为中毒、高毒和剧毒,最终处理后出水的毒性分别为无急性毒、中毒和微毒,对毒性的去除效率分别为96.4%、74.3%和99.5%。TIE结果表明,石化废水中的主要致毒物质是非极性有机物和可滤型物质。本研究结果为石化废水的综合生物毒性评价提供了研究基础,为探讨废水生物毒性的去除提供了实例参考。     

焦化废水A~2/O处理过程中的组成和毒性变化规律

焦化废水中含有大量毒性物质,具有较强的生物毒性。本文以实验室构建的A2/O焦化废水处理系统为研究对象,考察废水处理过程化学成分和急性毒性的变化。采用紫外扫描和三维荧光光谱分析考察了处理系统各阶段出水的物质组分,并采用固相萃取和超滤膜分离等手段对水样各组分的发光细菌急性毒性进行研究。结果表明,伴随着芳香族物质等毒物的去除,焦化废水的急性生物毒性在该处理系统中被逐步削减,最终出水的毒性当量仅为原水的28%;不同组分的生物毒性测试结果显示,废水水样的强极性和中等极性有机组分贡献了绝大部分的毒性当量,而这些物质主要在缺氧段及好氧段被削减;结合三维荧光光谱的分析结果,可推断焦化废水中一类很难在A2/O处理系统中被完全去除的芳香族蛋白质类似物(Ⅱ区)很可能具有较强的生物毒性,是构成出水毒性的主要物质。     

丘陵地区水稻田使用毒死蜱对水体的污染及其生态风险

选择丘陵地区的小规模水稻田作为试验地,调查毒死蜱在该区域水稻田中的使用时间和使用量,监测不同时期水稻田进出水中毒死蜱残留水平.结果显示,毒死蜱使用后水稻田出水中毒死蜱残留水平高于进水,最高达26.07μg.L-1.从河流引入的进水中也存在毒死蜱残留,最高达3.23μg·L-1,说明上游农田已经对河水产生了污染.毒死蜱对斑马鱼(Brachydanio rerio)、大型溞(Daphnia magna)和斜生栅列藻(Scenedesmus obliquus)的急性毒性测定结果分别为:斑马鱼,ρ(96h,LC50)为1.11mg·L-1;大型溞,ρ(48 h,EC50)为1.44μg·L-1;斜生栅列藻,ρ(72 h,EC50)为0.193 mg·L-1.根据欧盟急性毒性风险评价标准进行评估,结果表明毒死蜱对水稻田周边水体中鱼类和藻类为低风险,对大型溞为有风险.     

城市污水处理厂进出水中类雌激素暴露影响评价

以稀有鮈鲫（Gobiocypris rarus）为模型动物,利用卵黄蛋白原（VTG）和生长发育指标作为类雌激素污染的生物标志物,评价了沙湖污水处理厂进出水中类雌激素暴露对稀有鮈鲫仔鱼的影响.结果表明：暴露21d后,未稀释进水和一级处理出水对稀有鮈鲫仔鱼VTG有显著诱导,各级处理水对稀有鮈鲫的生长发育也造成了一定的影响,在进水和一级处理出水暴露组中有死亡现象发生.以17β-雌二醇（E2）为阳性对照,对稀有鮈鲫VTG的诱导作标准曲线,计算进水以及各级出水的类雌激素E2的活性当量,发现污水处理厂一级和二级处理工艺对污水的类雌激素活性的去除率分别为47%和95%以上.表明在现有污水处理工艺中,二级处理工艺可去除大部分的类雌激素,而一级处理工艺却不能有效去除类雌激素.     

代表性二级处理、三级处理和湿地生态修复技术对城镇污水人源干细胞毒性的削减

污水中的难降解污染物往往具有浓度低但毒性强的特点,可以通过多种暴露途径直接或间接对人体健康产生有害影响,因此有必要评估污水处理技术对健康效应的削减效果.本研究选择人骨髓间充质干细胞(human bone marrow mesenchy-mal stem cells,hBMSCs)体外模型,评估典型二级处理、三级处理和湿地修复技术进水、主要工艺排水的综合毒性,并与发光菌急性毒性测试结果进行比较.水样萃取物对hBMSCs的细胞毒性呈剂量依赖性关系,进水毒性单位(toxicity unit,TU)在0.03～ 0.22范围内,出水TU为0.02 ～ 0.03.二级处理技术对细胞毒性的削减率为59.8％.三级处理过程中经混凝、微滤和反渗透处理后,出水无显著细胞毒性,但经臭氧消毒后最终排水的细胞毒性较进水无显著变化.湿地修复技术对细胞毒性的削减率为49.9％.66.7％ (14/21)水样品对于hBMSCs细胞毒性的TU值高于发光菌急性毒性的TU值.在相对富集倍数(related fold enrichment,REF)20％效应浓度(EC20)下,二级处理和三级处理技术对污水hBMSCs细胞毒性的削减率低于发光菌急性毒性,但湿地修复技术对细胞毒性的削减率高于发光菌急性毒性.结果 提示污水处理厂排水中残留的难降解有机污染物对人源干细胞具有较强的有害效应,为再生水水质安全性评价以及城镇污水资源化技术研发提供参考依据和方法.     

利用重组大肠杆菌SOS法评价污水厂出水的遗传毒性以及工艺去除效果

SOS/umu测试法被广泛应用于化合物和复杂混合物遗传毒性的评价,由于该技术所用菌种为致病菌且操作步骤繁琐等原因,制约了技术的推广应用。研究建立了基于重组大肠杆菌SOS效应的水质遗传毒性检测方法(专利号:ZL201110022476.1),应用该方法评价了某市4座污水厂出水的直接遗传毒性效应,同时以污水处理一厂为例考察了直接遗传毒性效应的季节变化规律以及不同的工艺对水中直接遗传毒性物质的去除情况。结果显示:各污水厂出水均表现出一定的直接遗传毒性,对应的4-NQO毒性当量浓度范围为0.018~0.514 mg·L-1;一年四季中夏季进出水直接遗传毒性效应最高,现有工艺中生化处理工艺段对直接遗传毒性去除效果最佳,去除率为33.33%。该方法操作便利、检测敏感性较高、操作危险性较低,可用于水中直接遗传毒性效应的测试。     

基于毒性效应的间隙水致毒物质鉴别技术进展

沉积物作为污染物迁移转化过程中重要的"源"和"汇",与整个生态系统及人类健康有着密切联系。间隙水很大程度上反映了水体沉积物的污染状况,同时可以真实反映生物的实际暴露情况,间隙水中关键致毒物质的鉴别是科学准确地评价间隙水及沉积物毒性与风险的重要基础。毒性鉴别评估(Toxicity Identification Evaluation,TIE)和效应引导的污染物识别(Effect Directed Analysis,EDA)技术作为致毒物质识别的主要方法,已在沉积物和间隙水的致毒物筛选中得到了初步的应用。本文介绍并比较了常用的间隙水提取方法,总结了TIE和EDA在间隙水致毒物质异位及原位鉴别方面的应用与发展,及鉴别过程中使用到的基本毒性量化方法与其适用条件。在当前间隙水关键致毒物质识别研究的基础上,指出了异位分析难以避免毒性损失和有机污染物鉴别方面的局限等问题,并提出应推广原位毒性试验技术且进一步发展有机物的精细分离技术和质谱识别技术等发展方向。     

部分除草剂与重金属混合物对发光菌的毒性

以5种不同类型除草剂和4种重金属为混合物组分,探索混合物毒性变化规律.应用微板毒性分析方法,测定了百草敌、磺草灵、西草净、除草定、环嗪酮、CdCl2·2.5H2O、Ni(NO3)2·6H2O、CoSO4·7H2O和ZnSO4·7H2O对淡水发光菌—青海弧菌Q67(Vibrio qinghaiensis sp.—Q67)的发光抑制毒性.应用非线性最小二乘拟合技术模拟实验剂量-效应数据.结果表明,5种除草剂与4种重金属化合物的剂量-效应曲线(DRC)均可用Weibull函数有效表征.为了全面考察各种不同浓度组成的混合物对Q67的毒性,设计了9个组分同时存在的3个等效应浓度比(EECR)混合物和10个均匀设计浓度比(UDCR)混合物.同样应用微板毒性分析方法测定了各个混合物对Q67的抑制毒性,并应用非线性最小二乘拟合技术模拟了其剂量-效应曲线.通过剂量加和(DA)与独立作用(IA)模型综合分析了各个混合物对发光菌的毒性变化规律.结果表明,不同类型除草剂与多种重金属的各种浓度组合的混合物毒性均可用DA模型进行预测和评估.     

乐安江水和沉积物样品的生物毒性评估

采用二种发光菌发光抑制、二种藻生长抑制、大型溲生和慢性毒性多种生物测试方法。对采集于１９９３年６月，１９９３年１２月和１９９４１０月的乐安江可水、沉积物和沉积物间隙不进行了多指标生物毒性测试，在河流４０，５０和１５９ｋｍ处观测到较强毒性，研究结果：毒性排放主要来自乐安江上游德兴铜矿、洎不河，以及乐安江下游接近鄱阳湖口和沉积物中重金属的释放。     

Water Quality Criteria for European Freshwater Fish

1. For water pollution control purposes, the concentration-addition model for describing the joint effects of mixtures of toxicants on aquatic organisms is appropriate; in this model the contribution of each component in the mixture is expressed as a proportion of the aqueous concentration producing a given response in a given time (e.g. p 96-h LC50).

2. Examination of available data using this model shows that for mixtures of toxicants found in sewage and industrial effluents, the joint acutely-lethal toxicity to fish and other aquatic organisms is close to that predicted, assuming simple addition of the proportional contribution from each toxicant. The observed median value for the joint effect of these toxicants on fish is 0.95 of that predicted, and the corresponding collective value for sewage effluents, river waters, and a few industrial wastes, based on the toxicity of their constituents, is 0.85, while that for pesticides is 1.3.

3. The less-than-predicted effect of commonly-occurring toxicants in some mixtures may be partly attributable to small fractions of their respective LC50 values having a less-than-additional effect. However, recent research has shown that for some organic chemicals which have a common quantitative structure-activity relationship (QSAR), their joint action as determined by acute toxicity is additive at all concentrations.

4. The few (unpublished) data available for the long-term lethal joint effect on fish of toxicants in mixtures suggest that they may be markedly more than additive, a phenomenon that needs confirmation and further investigation.

5. In the few studies on the sub-lethal effects on fish (eg growth), the joint effect of toxicants has been consistently less-than-additive which suggests that as concentrations of toxicants are reduced towards the levels of no effect, their potential for addition is also reduced. There appear to be no marked and consistent differences between the response of different species to mixtures of toxicants.

6. Field studies have shown that reasonably accurate toxicity predictions based on chemical analysis can be made if the waters which are polluted are acutely lethal to fish, and that a fish population of some kind can exist where the median 2 p t LCSOs (rainbow trout) is < 0.2. It is not known whether this condition is equivalent to a C p NOEC of 4.0 (ie the sum of the individual fractions of the NOEC for the species present), or to a NOEC of < 1.0 for each individual toxicant (i.e. fractions of the NOEC are not summed).

7. In general, the joint effect of the common toxicants on lethal and sub-lethal responses of fish is not explained by variations in the uptake of the individual toxicants concerned; this may not apply for those chemicals with a common QSAR, although there is little experimental evidence in this field.

8. There is an immediate need for more empirical studies on the joint effect of mixtures of toxic units of individual components, and the relation between long- and short-term lethal and non-lethal joint effects. This applies to mixtures of commonly occurring toxicants as well as to mixtures of organic chemicals with a common QSAR. The data obtained should be reinforced by studies on the mechanisms of interaction of toxicants. More field studies which relate water quality to the structure and productivity of fish populations are also required, involving direct measurements of fractional toxicity of the river water wherever possible.

9. The concentration-addition model appears to be adequate to describe the joint effect of commonly-occurring constituents of sewage and industrial wastes, and for tentative predictions of the joint effect on fish populations of toxicants present at concentrations higher than the EIFAC recommended values. However, concentrations lower than the EIFAC recommended values may make an increasingly lesser contribution to the toxicity of mixtures of toxicants and there may be a need to adjust the tentative water quality criteria downwards where two or more toxicants are present at concentrations close to these values. For toxicants with a common QSAR, their additive joint action may necessitate the setting of water quality criteriafor this group as a whole and not on the basis of individual compounds. However, too little is known of their precise joint action where the combined concentration produces a sub-lethal response.     

有害结局路径(AOP)框架在水体复合污染监测研究中的应用

由于包含复杂的毒害化学污染物质,水体复合污染一直威胁着人类健康和水生生态安全。对复合污染水体进行监测、评估和治理是水环境管理的重点之一。监测并识别水体关键毒害污染因子是进行水质管理的前提,也是复合污染研究的难点。目前国内外在水复合污染毒性监测研究上主要基于动物活体试验或者生物体外测试。由于受限于毒理学测试方法,常见的应用通常仅关注于某方面的毒性效应或者少数的分子指标,因而受到质疑和挑战。有害结局路径(Adverse outcome pathway, AOP)的概念将化学污染物的结构、致毒的分子启动事件和生物毒性的有害结局建立关联,为污染物的毒性测试、预测和评估提供了新的模式。本文旨在论述有害结局路径在复合污染毒性评估和关键毒害物质鉴别中的指导性价值和意义。在有害结局路径的指导框架下,借助于生物体外高通量测试技术、化学分析的靶向和非靶向分析技术、和生物信息学技术,可以系统地分析化学混合物在分子、细胞水平上健康相关指标的响应水平,评估水体中复杂结构污染物,与不同生态和健康有害结局之间的关联,为水环境评价和优先污染物的筛选管理提供有效支撑。本文通过综述AOP框架在复合水体中毒害物质风险研究的现状和优势,对AOP在水环境环境管理上的应用前景提出展望。     

有害结局路径(AOP)框架在水体复合污染监测研究中的应用

水体复合污染包含低浓度、种类复杂的毒害化学污染物,威胁人类健康和生态安全。监测并识别水体关键毒害污染因子是进行水质管理的前提,也是复合污染研究的难点。目前国内外在水复合污染毒性监测研究上主要基于动物活体试验或者生物体外测试。由于受限于毒理学测试方法,常见的应用通常仅关注于某方面的毒性效应或者少数的分子指标,因而受到质疑和挑战。有害结局路径(Adverse outcome pathway,AOP)的概念将化学污染物的结构、致毒的分子启动事件和生物毒性的有害结局建立关联,为污染物的毒性测试、预测和评估提供了新的模式。本文旨在论述有害结局路径在复合污染毒性评估和关键毒害物质鉴别中的指导性价值和意义。在有害结局路径的指导框架下,借助于生物体外高通量测试技术、化学分析的靶向和非靶向分析技术和生物信息学技术,可以系统地分析化学混合物在分子、细胞水平上健康相关指标的响应水平,评估水体中复杂结构污染物,与不同生态和健康有害结局之间的关联,为水环境评价和优先污染物的筛选管理提供有效支撑。本文通过综述AOP框架在复合水体中毒害物质风险研究的现状和优势,对AOP在水环境环境管理上的应用前景提出展望。     

Inhibition character of crotonaldehyde manufacture wastewater on biological acidification

• The inhibition of the main organic pollutions in CMW was demonstrated. • Variations of AK and BK showed a high correlation with the SAA of Ac and n-Bu. • The inhibitory degree was in the order of Ac>n-Bu for individual toxicants. • Biodegradation products of the main toxicants were analyzed. This work aims to investigate the inhibitory effect of crotonaldehyde manufacture wastewater (CMW) on biological acidification. To reveal the inhibitory effect of wastewater to the anaerobic granular sludge (AnGS), variations of the specific acidogenic activity (SAA) and activities of key enzymes were investigated. The results indicated that the dosage of CMW causing a 50% effect concentration (EC₅₀) on the activity of total volatile fatty acids (TVFA) production was 380 mg COD/g VSS. The inhibitory effect of individual toxicants in CMW on the activity of TVFA production were in the order of crotonaldehyde>ethyl sorbate>(E,E)-2,4-hexadienal, and their inhibitory degrees on individual VFA products were acetic acid (Ac)>n-butyric acid (n-Bu), which could correspond to the variations in the activities of acetate kinase (AK) and butyrate kinase (BK). Furthermore, the combined effect of three toxicants on the activity of TVFA production was significantly higher than that of any individual toxicant, and the contribution of the relative toxicity to CMW was 77.27%. Additionally, the biodegradation products of the main toxicants indicated that the removal of crotonaldehyde and (E,E)-2,4-hexadienal was primarily due to the hydrogenation of alkene and aldehyde and the oxidation of aldehyde. Nevertheless, the removal of ethyl sorbate was primarily based on adsorption. In conclusion, biological acidification has a limited ability to treatment CMW, therefore, a further pretreatment technology should be used to remove the main toxicant of wastewater.     

Toxicity of zinc,cadmium and copper to the shrimp Callianassa australiensis. II. Effects of paired and triad combinations of metals

The acute toxicity of zinc, cadmium and copper to Callianassa australiensis (Dana) was assessed in paired and triad combinations in 14 d toxicity tests. Predicted mortalities following exposure to various mixtures of metals were evaluated according to two models proposed by Plackett and Hewlett (1967) for the noninteraction of toxicants: (a) independent dissimilar action and (b) simple similar action. However, based on the rejection of these two models and analyses of the experimental results for each metal alone, it was concluded that the metals in all paired mixtures acted in an interactive manner. For the triad mixture, mortalities of shrimp were predictable by the independent dissimilar action model. Toxicities of mixtures of metals were also assessed using the toxic-unit concept. However, mortalities in all mixtures were overestimated by this method. Some problems concerning the prediction of mortalities in mixtures of toxicants are discussed.Paper No. 245 in the Ministry for Conservation, Victoria, Environmental Studies Series     

“生物有效性测量”与“全沉积物毒性识别评估(TIE)”联用有效识别出沉积物中主要致毒污染物

沉积物中污染物种类繁多,准确判断其中产生生物毒性的主要来源是个难点,本文作者先采用TIE法初步判断出主要致毒污染物为有机物和重金属(毒性描述阶段(相I)),传统的毒性单位分析结果显示Cr、Cu、Ni、Pb和Zn主要致毒重金属,而为氯氰菊酯、氯氟氰菊酯、溴氰菊酯和氟虫腈为主要致毒有机物中(毒性鉴定阶段(相II))。采用4步分级提取法和Tenax提取法分析了重金属和有机物的生物有效性。生物有效性毒性单位分析更加准确地锁定了毒性主要贡献重金属为Zn、Ni和Pb,毒性主要贡献有机物为氯氰菊酯、氯氟氰菊酯和氟虫腈。沉积物的稀释降低了重金属的毒性并使其毒性贡献鉴定变得复杂,生物有效性测量可以有效地提高TIE结果的准确性。
精选自Xiaoyi Yi, Huizhen Li, Ping Ma and Jing You. Identifying the causes of sediment-associated toxicity in urban waterways in South China: Incorporating bioavailabillity-based measurements into whole-sediment toxicity identification evaluation. Environmental Toxicology and Chemistry: Volume 34, Issue 8, pages 1744–1750, August 2015. DOI: 10.1002/etc.2970
详情请见http://onlinelibrary.wiley.com/doi/10.1002/etc.2970/full     

“生物有效性测量”与“全沉积物毒性识别评估(TIE)”联用有效识别出沉积物中主要致毒污染物

沉积物中污染物种类繁多,准确判断其中产生生物毒性的主要来源是个难点,本文作者先采用TIE法初步判断出主要致毒污染物为有机物和重金属(毒性描述阶段(相I)),传统的毒性单位分析结果显示Cr、Cu、Ni、Pb和Zn主要致毒重金属,而为氯氰菊酯、氯氟氰菊酯、溴氰菊酯和氟虫腈为主要致毒有机物中(毒性鉴定阶段(相II))。采用4步分级提取法和Tenax提取法分析了重金属和有机物的生物有效性。生物有效性毒性单位分析更加准确地锁定了毒性主要贡献重金属为Zn、Ni和Pb,毒性主要贡献有机物为氯氰菊酯、氯氟氰菊酯和氟虫腈。沉积物的稀释降低了重金属的毒性并使其毒性贡献鉴定变得复杂,生物有效性测量可以有效地提高TIE结果的准确性。
精选自Xiaoyi Yi, Huizhen Li, Ping Ma and Jing You. Identifying the causes of sediment-associated toxicity in urban waterways in South China: Incorporating bioavailabillity-based measurements into whole-sediment toxicity identification evaluation. Environmental Toxicology and Chemistry: Volume 34, Issue 8, pages 1744–1750, August 2015. DOI: 10.1002/etc.2970
详情请见http://onlinelibrary.wiley.com/doi/10.1002/etc.2970/full