湖泊沉积物中有机磷酸酯阻燃剂污染特征及生态风险评价

利用气质联用仪（GC-MS）检测广州15个城市湖泊表层沉积物中16种有机磷酸酯阻燃剂（OPFRs）含量,分析其分布特征及来源,并评价其生态风险。结果表明,广州15个城市湖泊沉积物中16种 OPFRs总质量比（∑16OPFRs）范围为138ng/g～306ng/g,平均值为203ng/g,污染属于中等水平。TBEP、TCEP、TBP、TDCP为主要OPFRs,其中TBEP值最高。相关性研究表明,大部分OPFRs单体与总有机碳无显著相关性,OPFRs来源具有点源性特征。主成分分析表明,沉积物中 OPFRs 来源并不单一,游客产生的废弃塑料、大气沉降、污水排放、路面径流及污泥再利用等都可能成为其来源。生态风险评价表明,沉积物中OPFRs存在一定的生态风险。     

太滆运河表层沉积物中的酞酸酯类增塑剂和溴系、有机磷系阻燃剂残留特征初探

分别采用微波萃取-气相色谱/质谱法、加速溶剂萃取提取-液相色谱/质谱法对采自太滆运河5个沉积物样品中的6种邻苯二甲酸酯类(PAEs)、13种多溴联苯醚(PBDEs)和9种有机磷酸酯(OPEs)的质量比及分布进行研究。结果表明,所有样品中均检测到PAEs、PBDEs和OPEs(以总量计),其总质量比分别为1.99~6.90μg/g,47~572和17.1~69.7 ng/g;十溴联苯醚(BDE-209)和磷酸三异辛酯(TEHP)分别是质量比最高的PBDEs和OPEs;对于PAEs,入太湖点位处邻苯二甲酸二(2-乙基己基)酯(DEHP)质量比较高,其余点位则是邻苯二甲酸二正丁酯(DBP)质量比较高;ω(PAEs)、ω(PBDEs)和ω(OPEs)两两间线性相关性较好,指示其来源相同;下游沉积物中污染物的质量比均高于上游,沿岸生产、生活中增塑剂和阻燃剂对太湖的污染应引起更多关注。     

大伙房水库多介质中全氟化合物赋存特征、源解析及健康风险评估

大伙房水库属于全国城市供水九大重点水源地之一,作为辽宁省重要的饮用水水源地,库区水质直接影响该区域人民饮水安全及身体健康。对大伙房水库表层水体、沉积物和鱼类样品中全氟化合物（PFAS）的赋存特征及可能的来源进行分析,并运用健康风险商值法评估PFAS的潜在健康风险。结果表明,库区表层水体中ρ（ΣPFAS）为1.18~8.19 ng/L,主要污染物为全氟辛酸及其盐类化合物（PFOA）和全氟戊基羧酸（PFPA）,其浓度水平随时间呈下降趋势;沉积物中只检出3种污染物,分别为PFOA、全氟十一烷基羧酸（PFUnA）和全氟十二烷基羧酸（PFDoDA）,ω（ΣPFAS）为0.16~0.48 ng/g;不同鱼类样品中ω（ΣPFAS）由高到低依次为：武昌鱼（2.49 ng/g）>鲤鱼（2.30 ng/g）>白鲢（2.02 ng/g）>花鲢（2.01 ng/g）,主要污染物均为PFPA。基于主成分分析与相关性分析可知,大伙房水库库区的PFAS主要来自采矿、电镀、涂料等工业污染废水和生活污水;健康风险评估结果表明,表层水体和鱼类样品中的PFAS不存在健康风险。     

杭州夏季一次降雨过程雨水中全氟化合物及主要化学组分的变化特征

采用分段采样的方式收集杭州市2018年8月2日—3日一场降水样品,测定其中16种全氟化合物（PFCs）及主要化学组分浓度。结果发现,此次降雨过程水样的pH值范围为5.04～5.32,均为弱酸性降水,酸雨类型为复合型,检出的主要阳离子为NH+4,主要阴离子为SO2-4和NO-3;样品中检出7种中短链PFCs,包括2种全氟烷基磺酸（PFSAs）和5种全氟烷基羧酸（PFCAs）,ΣPFCs质量浓度范围为4.41 ng/L～25.2 ng/L,主要污染因子全氟辛酸（PFOA）质量浓度范围为096 ng/L～13.1 ng/L;降雨过程对大气污染清除作用的统计结果表明,区域大气环境中的主要化学组分及除全氟丁酸（PFBA）之外的PFCs污染主要吸附在云下大气颗粒物上;雨水中各污染因子浓度变化特征及相关性统计结果提示,杭州市大气中PFCAs和PFSAs两类PFCs可能来自不同的污染源。     

九洲江沉积物多环芳烃和抗生素的分布特征与风险评价

利用液相色谱-三重四级杆质谱法(HPLC-MS/MS)以及超高压液相色谱法(HPLC),于2018年1月对九洲江沉积物样品中31种抗生素和16种多环芳烃(PAHs)的分布特征进行研究并评价其生态风险。结果表明,九洲江沉积物检出20种抗生素,其中四环素类(TCs)抗生素质量分数最高,或因其在养殖业用量最大且易被沉积物吸附;滩面镇（S3点位）抗生素的总质量分数（52 ng/g）最高,与附近的滩面镇生猪养殖业发达,也与S3点位正好位于污水处理厂排口下游不远处有关;沉积物中共检出15种PAHs,温泉镇（S1点位）沉积物中PAHs的质量分数最高。沉积物中,4环PAHs占比最高,说明九洲江流域PAHs主要来源于煤和木柴的燃烧。生态风险评价结果表明,TCs抗生素处于高风险水平,且高风险点集中出现在滩面镇河段（S3点位）,需要采取措施减少TCs抗生素的使用;所有点位的PAHs的生态风险均为低风险,但有部分无安全剂量的PAHs组分被检出,对九洲江生态环境存在潜在威胁。     

骆马湖地区水体、沉积物中农药筛查和分布特征

采用气相色谱/质谱（GC/MS）非靶向筛查技术,分别于2019年11月5—7日（枯水期）、2020年4月24—26日（平水期）和2020年7月15—16日（丰水期）对骆马湖地区水体和沉积物中的农药残留进行了筛查并对其空间分布特征进行研究。结果表明,水中筛查出主要农药13种,除草剂占比62%,检出率＞95%的农药有丁草胺、环嗪酮、异丙甲草胺、多效唑、噻氟菌胺、稻瘟灵、毒死蜱、阿特拉津、避蚊胺和莠灭净,阿特拉津检出质量浓度最高（ND～10 599 ng/L,平均值为725.5 ng/L）,其次为多效唑（ND～2 089 ng/L,平均值为237.0 ng/L）和噻氟菌胺（ND～1 991 ng/L,平均值为237.2 ng/L）。与国内其他地区相比,骆马湖地区水中农药污染处于中等水平,其中阿特拉津、稻瘟灵和毒死蜱的生态风险值得重点关注。骆马湖及入湖河流水中农药总质量浓度呈现丰水期＞平水期＞枯水期的特点,与地表径流、农药的性质及其在水体中的释放等因素有关,丰水期入湖口和省界来水中农药对饮用水水源地的影响较大。沉积物中筛查出9种农药,总体含量不高,且仅扑灭净和避蚊胺检出率>95%,其余<20%。     

太湖以西常州区域水体中典型PPCPs污染特征

为进一步了解环太湖区域药品及个人护理用品（PPCPs）环境污染现状,于2016年9月对太湖以西常州区域水体中典型PPCPs污染水平进行了调查。利用高效液相色谱-串联质谱（HPLC MS/MS）检测分析了24种PPCPs在常州区域水体中的赋存和空间分布特征。结果表明,常州区域水体中24种目标PPCPs均被检出,PPCPs质量浓度总量范围为51.08～325.79 ng/L,20个监测点位中,红凌桥检出PPCPs总量最高,达325.79 ng/L;水体中优势污染物为双酚A和诺氟沙星,双酚A在黄埝桥检出的质量浓度最高,达158.53 ng/L,其次是新河口和红凌桥,质量浓度分别为65.57和57.86 ng/L;诺氟沙星在红凌桥检出的质量浓度最高,达75.12 ng/L。喹诺酮类抗生素、磺胺类抗生素在常州流域内基本呈均匀分布;激素类、大环内酯抗生素、神经镇痛类和心脏病类药物质量浓度与人口密度大致呈正相关。     

高效液相色谱串联质谱法测定某市污水处理厂进出水中的全氟化合物

通过建立直接进样-高效液相色谱串联质谱（HPLC-MS/MS）测定污水处理厂进出水中的10种全氟化合物的方法,了解污水厂进出水中全氟化合物污染情况。10种目标分析物在10~500 ng/L范围内具有良好的线性关系,方法检出限为2.3~8.3 ng/L,精密度为2.1%~7.1%,加标回收率为60.6%~91.7%。应用该方法测定某市典型污水厂进出水中的全氟化合物,进水中全氟化合物质量浓度为90.9~206 ng/L,主要污染物是PFOA、PFHxS和PFBS;出水中全氟化合物的质量浓度为67.4~158 ng/L,环境排放量为6.7~22.9 g/d,主要污染物是PFOA和PFHxS。结果表明,该方法能很好地适用于复杂基质中10种全氟化合物的检测。     

山东省主要河流中抗生素污染组成及空间分布特征

采用固相萃取-液相色谱/串联质谱法研究了山东省境内四大流域主要河流中抗生素污染组成及空间分布特征,涉及我国用量最大的6类共20种抗生素。结果表明:20种抗生素均有检出,且大环内酯类、喹诺酮类和四环素类抗生素整体检出浓度较高。就流域而言,半岛诸河流域抗生素污染较小,平均总质量浓度61.4 ng/L;海河流域、小清河流域和淮河流域相对较为严重,平均总质量浓度分别为232、175、118 ng/L。抗生素空间分布呈现一定的规律,检出浓度较高的点位主要集中在人口密集区下游,抗生素污染与周边生活污水、养殖企业废水和城市污水处理厂排水密切相关,而且抗生素组成可从一定程度上反映出污染来源。     

武汉市巡司河中抗生素分布特征及生态风险评价

采用大体积直接进样—超高效液相色谱串联质谱法分析武汉市巡司河中45种抗生素的存在水平,评估其可能存在的生态风险。在巡司河布设6个采样点,于2022年12月—2023年5月进行采样并分析。结果显示,6个采样点共检出27种抗生素,检出最大质量浓度为874.2 ng/L;其中,氧氟沙星、左氧氟沙星检出率均为100%。监测期间,12月抗生素平均质量浓度最高（101.05 ng/L）,4月最低（25.87 ng/L）。6个点位中,点位S3与S5抗生素平均质量浓度高于其他点位,分别为1 721.20和1 734.07 ng/L;点位S4是巡司河与长江的交汇处,抗生素平均质量浓度最低（94.54 ng/L）。利用风险商值法对巡司河中抗生素生态风险开展评价,结果表明：氧氟沙星、罗红霉素和克拉霉素呈现出较高风险,左氧氟沙星、林可霉素和莫西沙星在大多数点位处于中等风险,其余几种抗生素风险较低。     

Size Distribution of Aerosols (PM10) and Lead (Pb) near Traffic Intersections in Mumbai (India)

The size distribution of aerosols was measured near traffic intersections of Marol link road in air quality control region (AQCR1), which is a moderately industrial area and Dadar Khodad circle in AQCR2, which is a heavily commercial core of the Mumbai City. The reason behind selecting the two unidentical regions was to study the contribution from vehicles to the size separated PM10 and that of Pb. It is recognised that particulates in urban air are responsible for serious health effects. As very small particles are assumed to be important for the adverse health effects, the particle size distribution is thus an important factor that needs to be addressed whenever the particulates pollution is concerned. The size measurements were done with a cascade impactor of eight stages with a back-up filter. It effectively separates the particulate matter into nine-sizes ranging from 0.0-0.4 to 9.0-10.0 microm. Samples were analysed in nine-particle size fractions with special reference to a toxic metal - lead (Pb) by atomic absorption spectrophotometry (AAS). It was found that PM10 and Pb at both the intersections could easily be classified by the size distribution. The fractions of the PM10 and that of Pb showing a tendency of trimodal distributions with the first peak at coarse mode approximately 9.0-10.0 microm, second at approximately 5.8 microm and the third at coarse mode approximately1.1 microm. The significant percentage of Pb was found in the range below 2.5 microm at both the intersections. However, Pb in AQCR1 is found in the coarser range as well, which could probably be the influence of various industrial activities in the area. PM10 concentration values in the coarser range in AQCR2 are associated with the resuspension of dust particles and mechanical erosions.     

Essential (Cu) and nonessential (Cd and Pb) metals in ichthyofauna from the coasts of Sinaloa state (SE Gulf of California)

With the aim of giving an overview on concentration and distribution of Cd, Cu, and Pb in fish from the coasts of Sinaloa state (SE Gulf of California), specimens with different feeding habits were collected in five locations. Sampling occurred between June 2003 and March 2004. Metal analyses on fish tissues were made by graphite furnace (Cd, Pb) and flame (Cu) atomic absorption spectrophotometry. Metal concentrations in tissues of carnivorous fish were grouped together and compared with corresponding concentrations in non-carnivorous fish; Cu and Pb levels were significantly (p?<?0.05) higher in liver of non-carnivorous species. Though no samples exceeded the maximum level set in international legislation for fish, from the perspective of the public health and considering the legal limits of fishery products for human consumption, Cu concentrations were exceeded (in tissues different from muscle) in four carnivorous and five non-carnivorous species according to the Australian legislation. In the case of Cd, two carnivorous species (Pomadasys leuciscus and Caulolatilus princeps) and one non-carnivorous species (Mugil cephalus), showed concentrations over the maximum level of 2 μg g^???1 dry weight considered in the Mexican legislation. Considering average amounts of fish consumption in Mexico, daily mineral intake (DMI) values for Cu and percentage weekly intake (PWI) of Cd and Pb were estimated; none of the analyzed metals in edible portion of analyzed fish could be detrimental to humans.     

Occurrence of polychlorinated dibenzo-p-dioxins and dibenzofurans (PCDD/Fs), polychlorinated biphenyls (PCBs) and polybrominated diphenyl ethers (PBDEs) in Lake Maggiore (Italy and Switzerland)

Samples of air (gas and particulate phases), bulk deposition, aquatic settling material and sediments were collected in Lake Maggiore (LM) in order to determine their content of polychlorinated dibenzo-p-dioxins and dibenzofurans (PCDD/Fs), polychlorinated biphenyls (PCBs) and polybrominated diphenyl ethers (PBDEs). Air (gas and particulate phases) concentrations were 0.5 pg m(-3), 80 pg m(-3), 13 pg m(-3) and 106 pg m(-3) for SigmaPCDD/Fs, SigmaPCBs, Sigma dioxin-like PCBs (DL-PCBs) and SigmaPBDEs, respectively. Deposition fluxes ranged from 0.7 ng m(-2) d(-1) for SigmaPCDD/Fs to 32 ng m(-2) d(-1) for SigmaPCBs. Aquatic settling material presented concentrations of 0.4 ng g(-1) dry weight (dw) for SigmaPCDD/Fs, 13 ng g(-1) dw for SigmaPCB, 3.4 ng g(-1) dw for SigmaDL-PCBs and 5.7 ng g(-1) dw for SigmaPBDEs. Mean sediment concentrations were 0.4 ng g(-1) dw for SigmaPCDD/Fs, 11 ng g(-1) dw for SigmaPCB, 3 ng g(-1) dw for SigmaDL-PCBs and 5.1 ng g(-1) dw for SigmaPBDEs. Similar PCDD/F and DL-PCB congener patterns in all the environmental compartments of LM point to an important, if not dominant, contribution of atmospheric deposition as source of these pollutants into LM. In contrast, PBDE congener distribution was not similar in the different environmental compartments. BDE 47 dominated air and settling material, while BDE 209 was the predominant congener in the bulk atmospheric deposition. Moreover, sediments showed two distinct PBDE congener profiles. Lower PBDE concentrated sediments were dominated by congeners 47 and 99, while BDE 209 dominated in higher PBDE concentrated samples. This suggests the influence of local sources as well as atmospheric input of PBDEs into LM.     

Biomonitoring of heavy metals (Cd,Hg, and Pb) and metalloid (As) with the Portuguese common buzzard (Buteo buteo)

The accumulation of heavy metals in the environment may have a wide range of health effects on animals and humans. Thus, in this study, the concentrations of arsenic (As), cadmium (Cd), lead (Pb), and mercury (Hg) in the blood and tissues (liver and kidney) of Portuguese common buzzards (Buteo buteo) were determined by inductively coupled plasma-mass spectrometer (ICP-MS) in order to monitor environmental pollution to these elements. In general, Hg and As were the elements which appeared in the highest and lowest concentrations, respectively. A highest percentage of non-detected concentration was found for blood Cd (94.6 %) but, in turn, it was the only metal that was detected in all kidney samples. The kidney was the analyzed sample which showed the highest concentrations of each element evaluated. Statistically, significant differences among blood, liver, and kidney samples were observed for As and Cd (P?相似文献   

Speciation of As(III) and As(V) in water and sediment using reverse-phase ion-pair high-performance liquid chromatography-neutron activation analysis (HPLC-NAA)

Total As content and the As species distribution in water and sediments from the Kwabrafo stream, a major water body draining the Obuasi gold mining community in southwestern Ghana, have been investigated. Total As content was determined by instrumental neutron activation analysis (INAA). Ion-pair reverse phase high-performance liquid chromatography-neutron activation analysis (HPLC-NAA) was used for speciation of As species. Solid phase extraction with phosphate buffer was used to extract soluble As species from lyophilized sediment. The mass balance after phosphate extraction of soluble As species in sediment varied from 89 to 96 %. Compositionally appropriate reference material International Atomic Energy Agency (IAEA)-Lake Sediment (SL)-1 was used to check the validity of INAA method for total As determination. The measured values are in good agreement with the IAEA recommended value and also within the 95 % confidence interval. The accuracy of the measurement in terms of relative deviation from the IAEA recommended value was ±0.83 %. “In-house” prepared As(III) and As(V) standards were used to validate the HPLC-INAA method used for the As species determination. Total As concentration in the water samples ranged from 1.15 to 9.20 mg/L. As(III) species in water varied from 0.13 to 0.7 mg/L, while As(V) species varied from 0.79 to 3.85 mg/L. Total As content in sediment ranged from 2,134 to 3,596 mg/kg dry mass. The levels of As(III) and As(V) species in the sediment ranges from 138 to 506 mg/kg dry mass and 156 to 385 mg/kg dry mass, respectively.     

Occurrence of haloacetic acids (HAAs) and trihalomethanes (THMs) in drinking water of Taiwan

In this study, water samples were collected from 86 water treatment plants for analysis of haloacetic acids (HAAs) and trihalomethanes (THMs) from February to March, 2007 and from July to August, 2007. Both seasonal and geographical variations of disinfection by-products (DBPs) in drinking water of Taiwan were presented. The results showed that the five HAA concentrations (HAA5) were 1.0–38.9 μg/L in the winter and 0.2–46.7 μg/L in the summer; and the total THMs were ND-99.4 μg/L in the winter and ND-133.2 μg/L in the summer. For samples taken from the main Taiwan island, dichloroacetic acid (29.4–31.7%) and trichloroacetic acid (25.3–27.6%) were the two major HAA species, and trichloromethane was the major THM species (49.9–62.2%) in finished water. For water treatment plants located on the offshore islands outside of Taiwan, high bromide concentration was found in raw water, and higher percentage of brominated THMs and HAAs were formed in the overall formation. A statistically significant (P?<?0.005) logarithmic linear regression model was found to be useful to describe the correlations between TTHM and HAA5 or nine HAAs (HAA5?=?1.219 ×TTHM ^0.754, R ²?=?0.658; HAA9?=?1.824 ×TTHM ^0.735, R ²?=?0.678). No apparent difference was observed for DBPs concentrations between finished water and distribution samples in this study.     

典型新兴环境污染物的研究进展

概述了内分泌干扰物(EDCs)、药物及个人护理品(PPCPs)等典型新兴环境污染物的主要类型、环境浓度、分析方法、来源与归趋以及国内外研究进展。内分泌干扰物、药物及个人护理品在世界各地的污水处理厂出水中检出,表明了污水处理技术的不完善性,亟需研究并应用更全面的污水处理技术,以从源头上阻断新兴环境污染物对环境的污染。     

Residual fate and persistence of endosulfan (50 WDG) in Bengal gram (Cicer arietinum)

A detailed study has been presented on heavy metal content of the Iture Estuary. Waters of the Sorowie and Kakum rivers that supply water into the Estuary were investigated to ascertain heavy metal pollution levels due to anthropogenic activities. Concentration s of Cd, Zn, Se and Pb were measured. The study shows pre-occupying pollution levels that constitute a threat to both terrestrial and aquatic ecosystems. The abundance of metals in the Estuary is in the order Zn > Pb > Cd > Se. The level of Cd in the Iture Estuary ranged between 0.011 mg/l and 0.041 mg/l while Se was in the range 0.018 mg/l to 0.029 mg/l, Pb 0.020 mg/l to 0.075 mg/l and Zn 0.040 to 2.45 mg/l. The impact of contaminated water from the Sorowie River on the Iture Estuary was outstanding and the study points out the importance of the Sorowie River as a primary pollution source to the Iture Estuary. The pollution of the Iture Estuary was found to be connected to human activities in its catchments.     

Effect of temperature on single and competitive adsorptions of Cu(II) and Zn(II) onto natural clays

This study conducted a combined adsorption-sequential extractionanalysis (CASA), by which five phases (i.e., exchangeable, carbonate, Mn-Oxide, organic, and Fe-Oxide phases) of adsorbed heavy metals were analyzed, to investigate temperature effects on single and competitive adsorptions of Zn(II) and Cu(II) ontonatural clays. In the case of single adsorption of Zn, the exchangeable phase adsorption decreased from 65 to 40%, but thecarbonate phase adsorption increased from 30 to 40%, with an increase in temperature from 15 to 55 °C. However, in itscompetitive adsorption with Cu, Zn was mostly present in the exchangeable phase (over 90%), and with an increase in temperature, the exchangeable phase adsorption decreased only 10%. In the case of Cu, over 50% among the total amount of adsorption was present in the carbonate phase in both cases ofsingle and competitive adsorptions. The carbonate phaseadsorption of Cu increased from 56 to 61% and from 60 to 66% in single and competitive adsorptions, respectively, with atemperature increase. These results show that in the case of Zn,the major mechanism of retention in natural clay soils might beexchangeable phase adsorption, especially in the case of competitive adsorption with Cu. However, in the case of Cu, the major mechanism might be carbonate phase adsorption, which is known to be a more immobile phase than exchangeable phase adsorption. It seems that the adsorption of Zn and Cu onto natural clays is an endothermic reaction, which represents thatthe adsorption equilibrium constants and capacities increase with a temperature increase, with the exception of exchangeablephase adsorption.     

Biosorption of Pb(II) and Cr(III) from aqueous solutions: breakthrough curves and modeling studies

The sorption capacity parameters obtained for batch studies provide useful information about biosorption system. However, such data fail to explain the process under continuous-flow conditions. The present study is an attempt to explore the biosorption of Pb(II) and Cr(III) by straw from local wheat (Triticum aestivum). The biosorbent has been characterized by using Fourier transform infrared spectroscopy and surface area and elemental analyses and found to be porous and polyfunctional. S-shaped breakthrough curves were obtained at different column heights for the both metal ions. Various breakthrough parameters and saturation times have been determined. The column data have been successfully used to study the Bohart–Adams' bed depth service time (BDST) model and Yoon and Nelson's model. It was found that BDST model quite efficiently explained the whole column data whereas Yoon and Nelson model could explain it below 90 % breakthrough concentration. The predicted and calculated BDST parameters were in agreement with each other. Yoon and Nelson's constant decreased with an increase in the column height for both metal ions. Effect of change in flow rate on the Pb(II) biosorption has also been discussed with respect to BDST approach.