渤海油气区周边海域PFASs的赋存特征与来源

为了解我国海上油田区域附近PFASs(多氟或全氟化合物)污染状况,本文针对我国渤海油田区所在海域采集了92个海水样品,并对其中19种PFASs及其新型替代品的含量进行了分析。结果表明,渤海油气区周边海水中总PFASs浓度范围为9.33~113ng/L,与中国其他海域相比,渤海油田区周边海水中总PFASs含量较高。传统PFASs中,全氟辛酸(PFOA)是大部分样品中的主要PFASs。新型替代品中,六氟环氧丙烷二聚酸(HFPO-DA)的浓度相对较高,浓度中位数为1.82ng/L,而在所有样品中6:2氯代多氟醚磺酸(6:2Cl-PFESA)均未检出。从区域分布来看,总PFASs浓度较高的油田位于渤海西部。总PFASs含量与离岸距离等影响因素相关性分析表明,渤海油气区附近海水中总PFASs含量与离岸距离显著相关,说明陆源是渤海油气区中PFASs污染的主要来源。     

Anthropogenic contaminants in freshwater from the northern Antarctic Peninsula region

This study aimed to evaluate the presence of ultraviolet filters (UV-Fs), benzotriazoles, pyrethroids and per- and polyfluoroalkyl substances (PFASs) in freshwater and wastewater from the northern Antarctic Peninsula region. All water samples analyzed contained UV-Fs residues and high concentrations were detected in anthropogenic impacted sites (< LOD up to 1300 ng/L). Likewise, benzotriazoles were detected in all water samples (< LOQ–920 ng/L). Regarding suspended particulate matter, almost all UV-Fs and all benzotriazoles were measured at concentrations ranging from < LOQ to 33 µg/g dry weight. Pyrethroids were also detected (< LOQ–250 ng/L) and their presence implies the existence of a gateway to the Antarctica Peninsula from other regions. The data confirmed the presence of PFASs (< LOD–7500 ng/L) in this area, in agreement with previous studies. In light of these results, extended monitoring in Antarctica should be carried out to perform a reliable environmental risk assessment leading to propose recommendations to minimize the anthropic impact.Electronic supplementary materialThe online version of this article (10.1007/s13280-020-01404-x) contains supplementary material, which is available to authorized users.     

强化生物除磷系统中胞外聚合物的特性

胞外聚合物(EPS)在生物除磷过程中具有蓄磷能力,为进一步明确生物除磷系统中的EPS特性,以不具有明显除磷能力的全程好氧活性污泥系统(R1)的EPS作为对比,考察了具有良好除磷效果的厌氧/好氧交替下的强化生物除磷系统(R2)中EPS的理化特性.结果表明,相对于R1中的EPS主成分在一个周期内的不固定,R2中的蛋白质含量一直明显高于多糖含量;两者的主要荧光物质均为类蛋白质和类富里酸,但在好氧末期R2中类蛋白质的荧光强度高于R1; R1的EPS中Ca2+> Mg2+,而在R2中, Mg2+>Ca2+,同时R1中的Ca2+含量平均值为8.67mg/gMLSS,大于R2中Ca2+的平均值2.40mg/gMLSS;在好氧末期,R2中的TP为21.65mg/gMLSS,明显高于R1中的TP含量(13.83mg/g-MLSS).此外,R1和R2的zeta电位平均值分别为-36mV和-25mV.由此可见, EBPR系统中的EPS具有与全程好氧活性污泥中的EPS不同的特征.     

大庆油田采油污水对斑马鱼过氧化氢酶的影响研究

为研究大庆油田采油污水对生物过氧化氢酶（Catalase,CAT）的毒性效应,判定采油污水对生物体的损害程度.以斑马鱼为实验材料,利用大庆油田不同稀释倍数（66.7倍、52.6倍、33.3倍）的采油污水胁迫培养斑马鱼,通过紫外分光光度法测定斑马鱼的不同部位CAT的变化情况,研究采油污水对斑马鱼毒性效应.结果表明,在相同的处理时间和环境条件下,随着采油污水稀释倍数的减小,斑马鱼的不同部位的CAT含量呈增加趋势,当达到一定稀释倍数时CAT的增长发生抑制,CAT含量减少,斑马鱼的生理状况也随之产生变化,甚至死亡.为此需要重视对大庆油田采油污水排放的监管、规范和治理.     

基于Meta分析的全氟化合物对鱼类生态毒性效应

全氟及多氟化合物（PFAS）是难降解的有机污染物,具有普遍存在、生物蓄积和生物学毒性效应等特点.为探讨PFAS对鱼类的生物毒性效应,综述了64篇文献,通过Meta分析合并效应值探讨鱼类暴露于PFAS对其功能性状的毒性,为PFAS的毒性评估提供参考,有利于PFAS污染的优先控制管理.结果表明：①在研究的12种功能性状中,鱼类的7类功能性状易感,毒性响应顺序为畸形（lnRR=-2.5599）、发育（lnRR=-0.4103）、细胞损伤（lnRR=-0.3962）、生殖（lnRR=-0.3724）、甲状腺水平（lnRR=-0.2492）、生长（lnRR=-0.2194）和生存（lnRR=-0.2192）;②鱼类性别和所处发育阶段显著影响PFAS的水生毒性,PFAS易对雌鱼产生不良影响（lnRR=-0.1628）,且胚胎期鱼类的生理功能受PFAS影响最显著（lnRR=-0.3553）;③研究涉及的PFAS共13种,其中具有磺酸盐基团的PFAS和长链PFAS更易对鱼类的功能性状产生不良影响（P<0.05）;④现有数据揭示PFAS在中低浓度（0.01~10 mg ·L^-1）下易对鱼类产生急性毒性（P<0.05）.     

基于自适应蚁群算法的化工园区毒气泄漏事故疏散路径规划*

为了降低人员在化工园区毒气泄漏事故中的伤亡风险,提出1种综合考虑疏散路径距离和毒性负荷值的自适应蚁群算法。通过建立路径评价函数,将疏散路径的毒性负荷值引入蚁群算法中,改进算法的信息素更新策略,采用启发式因子自适应调整策略并改进算法的启发式函数。运用Matlab软件进行仿真,将算法应用到某化工园区毒气泄漏事故中。研究结果表明:该自适应蚁群算法可以保持较高的搜索速度,在寻找距离最短道路的同时避开毒性负荷较高的疏散路径,可为化工园区毒气泄漏事故的应急疏散路径规划提供参考。     

Mountaintop Removal as a Case Study: The Possibilities for Public Advocacy through Virtual Toxic Tours

This paper argues that geo-spatial technologies (GST) such as Google Earth and Google Maps offer the potential for environmental advocates to generate virtual toxic tours. By analyzing the use of GST by I Love Mountains, a coalition of organizations attempting to stop the practice of mountaintop removal, this paper illustrates how a virtual tour generated through GST such as Google Earth can be a means to generate presence and promote identification between those local residents impacted by the practice and those who inhabit places seemingly distant from the same practice. The study not only acknowledges the limits of virtual tours but also identifies specific qualities not evident in tours of physical environments. Due to the potential virtual tours, this study also seeks to prompt further consideration of the use of GST and their role in contemporary environmental advocacy efforts.     

膜分离腐殖质前后晚期渗滤液可生化性的变化

晚期渗滤液由于含有大量难降解有机物腐殖质,可生化性差,较难处理。采用特定分子量的超滤膜对晚期渗滤液中的腐殖质进行有效的分离,研究了膜分离腐殖质前后渗滤液的可生化性的变化：渗滤液中腐殖质类物质去除率为90．7％,BOD5/COD值提高了6倍,可生物降解的有机物在总有机物中所占比率提高了约4倍。结果表明,分离腐殖质可提高渗滤液的可生化性。     

Interaction and combined toxicity of microplastics and per- and polyfluoroalkyl substances in aquatic environment

● Adsorption of PFASs on MPs and its mechanisms are critically reviewed. ● MPs could alter the transport and transformation of PFASs in aquatic environments. ● Combined toxicity of MPs and PFASs at organismal and molecular levels is discussed. Microplastics (MPs) are recognized as vectors for the transport of organic contaminants in aquatic environments in addition to their own adverse effects on aquatic organisms. Per- and polyfluoroalkyl substances (PFASs) are widely present in aquatic environments due to their widespread applications, and thus coexist with MPs. Therefore, we focus on the interaction of MPs and PFASs and related combined toxicity in aquatic environments in this work. The adsorption of PFASs on MPs is critically reviewed, and new mechanisms such as halogen bonding, π-π interaction, cation-π interactions, and micelle formation are proposed. Moreover, the effect of MPs on the transport and transformation of PFASs in aquatic environments is discussed. Based on four typical aquatic organisms (shellfish, Daphnia, algae, and fish), the toxicity of MPs and/or PFASs at the organismal or molecular levels is also evaluated and summarized. Finally, challenges and research perspectives are proposed, and the roles of the shapes and aging process of MPs on PFAS biogeochemical processes and toxicity, especially on PFAS substitutes, are recommended for further investigation. This review provides a better understanding of the interactions and toxic effects of coexisting MPs and PFASs in aquatic environments.     

沱江流域典型及新兴全氟/多氟化合物的污染特征及来源解析

为研究沱江流域表层水中全氟/多氟化合物（PFASs）的污染特征和来源,采用超高效液相色谱-串联质谱（UPLC-MS/MS）分析了沱江48个表层水样中的PFASs.结果表明,沱江流域水体中ρ（ΣPFASs）为12.5~3789 ng·L^-1,其中全氟辛烷羧酸（PFOA）为最主要污染组分,ρ（PFOA）为9.97~3764 ng·L^-1,占比高达73.6%~99.8%,说明传统PFASs仍是沱江流域主要的PFASs.所涉新兴PFASs检出率最高的为F-53B,检出率达100%,F-53B已在沱江流域被广泛使用.沱江流域浓度最高的新兴PFASs为6：2氟调聚磺酸（6：2 FTS）［nd~27.3 ng·L^-1,平均值为（9.12±7.70） ng·L^-1］,与国内外其它河流相比,处于较高污染水平.工业园区附近采样点的PFASs污染水平较高,其次为沱江下游的泸州河段,说明氟工业园区排放和人类日常生产活动是造成沱江流域PFASs污染的主要影响因素.最后,通过估算得出,沱江流域水相向长江排放的PFASs通量为353 kg·a^-1,其中排放通量最高组分为PFOA （348 kg·a^-1）,可为沱江流域PFASs管控提供基础数据.