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.     

Atmospheric deposition of polybrominated dibenzo-p-dioxins and dibenzofurans in Guangzhou, China: seasonal variations and sources

The atmospheric deposition of polybrominated dibenzo-p-dioxins and dibenzofurans (PBDD/Fs) was investigated at four locations in different suburban and urban functional districts of Guangzhou City. The annual deposition fluxes of total PBDD/Fs (eight 2,3,7,8-substituted tetra- to hexa-BDD/Fs) were in the range of 36-51 (mean 46) pg m(-2) day(-1), and the corresponding TEQ fluxes were estimated to range between 7.9 and 11.3 (mean 10.3) pg I-TEQ m(-2) day(-1), indicating a noticeable pollution level. The deposition fluxes of PBDD/Fs during the wet season were 2-4 times as high as those during the dry season. Both rainfall and temperature positively correlated with PBDD/F deposition fluxes. Ambient gas/particle partition coefficients (K(p)) were predicted with SPARC. It appears seasonal variations of PBDD/F deposition fluxes were influenced by meteorological parameters and the local usage of brominated flame retardants (BFRs). The congener profiles of PBDD/Fs at four locations were similar either spatially or temporally, indicating that the main PBDD/F emission sources were similar to one another. Seasonal variations and congener patterns of PBDD/Fs indicated the possible sources included electronic waste recycling, industrial waste incinerators and products containing BFRs.     

Concentrations and accumulation profiles of PCDDs, PCDFs and dioxin-like PCBs in adipose fat tissues of Korean women

Reports on residue levels and accumulation profiles of polychlorinated dibenzo-p-dioxins and dibenzofurans (PCDD/Fs) and dioxin-like polychlorinated biphenyls (DL-PCBs) in human adipose tissue are scarce in Korea. In this study, concentrations and accumulation features of PCDD/Fs and DL-PCBs were determined in the samples of adipose tissue collected from Korean women in 2007-2008. The total dioxin-like toxic equivalent (TEQ) concentrations (3.4-42 pg g(-1) lipid wt) in Korean adipose tissues were similar to those reported in European and other Asian countries. The relative contributions of individual compounds to total TEQs were as follows: non-ortho PCBs (mean: 45%) > PCDFs (28%) > PCDDs (24%) > mono-ortho PCBs (3%), a pattern similar to those reported for seafoods in Korea. The dominant PCDD/F congeners found in adipose tissues were OCDD and 2,3,4,7,8-PeCDF and dominant PCBs were 118, 156 and 105. No correlation was found between subject's age and concentrations of dioxin-like contaminants. Body mass index was not correlated with concentrations of PCDD/Fs and was negatively (p < 0.001) correlated with concentrations of DL-PCBs. The results of this study provide baseline information on PCDD/Fs and DL-PCBs in adipose tissues of the general population in Korea.     

Persistent organic pollutants in sediment from the southern Baltic: risk assessment

The concentrations of organochlorine pesticides, PCBs, and PCDD/Fs were measured in sediment samples collected from the Gulf of Gdańsk, the Gdańsk Deep, the Vistula Lagoon and the off-shore waters in the southern Baltic Sea. The determinations were conducted in the fraction <63 μm. The highest levels of pollutants were found in sediments from the Gulf of Gdańsk and the Gdańsk Deep. In these sediments, concentrations of pp'-DDT and its metabolites (pp'-DDE and pp'-DDD) ranged from 2 to 11 μg kg(-1) dw. Concentrations of HCB were between 0.1 and 1.0 μg kg(-1) dw. Concentrations of the sum of α-, β-, γ-HCH were between 0.3 and 2.58 μg kg(-1) dw. Concentrations of marker PCBs ranged from about 2 to 11 μg kg(-1) dry weight. Total TEQ PCDD/F/dl-PCB values in the studied samples varied between 1 and 18 ng kg(-1) dw. The data were evaluated in terms of ecotoxicological criteria based on the environmental impact of the pollutant effects. Our research indicated that in the sediment from the southern Baltic Sea, the PCDD/F and PCBs occurred at concentrations which could be dangerous to marine organisms.     

深圳市大气中PCDD/Fs污染水平初步研究

目的:了解深圳市大气中二噁(PCDD/Fs)的污染水平和分布特征。方法:利用大流量空气采样器分别采集6个采样点的空气样品,每个采样点采集两个平行样品。参照美国环保总局(US EPA Method TO-9A)二噁的检测方法,通过高分辨气相色谱-高分辨双聚焦磁式质谱仪(HRGC/HRMS)对大气样品中17种具有毒性当量因子(TEF)的单体进行了定性和定量分析。结果:∑PCDD/Fs的浓度范围为0.23～11.88pg/m3(平均值为3.84 pg/m3)。毒性当量浓度范围为0.014～0.29 pg I-TEQ/m3(平均值为0.135 pg I-TEQ/m3)。OCDD、HpCDD、HpCDF、OCDF、HxCDF是丰度较大的单体,分别占总浓度的48.21%、15.85%、11.37%、7.40%、6.59%。PCDDs和PCDFs单体浓度(除OCDF之外)均随氯原子取代个数的增加而增大。2,3,4,7,8-PeCDF对总的毒性当量贡献最大,占总毒性当量浓度的38.87%。六个采样点中有三个地点二噁同系物分布显示了"源"的特征,而另外三个地点则显示了"汇"的特征。成人的PCDD/Fs暴露量为0.0023～0.047 pg I-TEQ/kg.day;儿童PCDD/Fs暴露量为0.0052～0.11 pg I-TEQ/kg.day。结论:深圳市大气样品中二噁浓度低于国内一些城市研究水平,而高于日本、欧美国家的研究水平。     

Levels and distribution of PCDD/Fs, dl-PCBs, and organochlorine pesticides in sediments from the lower reaches of the Haihe River basin, China

The concentrations of polychlorinated dibenzo-p-dioxins and dibenzofurans (PCDD/Fs), dioxin-like polychlorinated biphenyls (dl-PCBs), and organochlorine pesticides (OCPs) in surface sediments from the lower reaches of the Haihe River basin, northern China, were determined by high-resolution gas chromatograph–high-resolution mass spectrometer. The concentrations of 2,3,7,8-substituted PCDD/Fs, dl-PCBs, and total OCPs [sum of hexachlorobenzene, hexachlorocyclohexanes, and dichlorodiphenyltrichloroethane (DDTs)] in 17 sediment samples were in the ranges of 11.6–1,180,924 pg/g dry weight (dw), 18.7–50,017 pg/g dw, and 1.7–35,280 ng/g dw, respectively. The contamination levels in the samples varied significantly between the different sites. Abnormally high concentrations of PCDD/Fs, dl-PCBs, and some OCPs were found in sediments from the lower reaches of the main channel of the Haihe River and the Dagu Drainage River, which were attributed to the historical production of pentachlorophenol and other pesticides near these locations. High levels of DDTs were detected in the Yongding New River sediment, which were likely to have originated from the discharge of wastewater from a dicofol factory upstream. In samples taken from other sites, the concentrations of these pollutants were at levels comparable to those documented in other areas of China. This preliminary investigation suggests that historical pesticide production in the Haihe River basin has contributed significantly to the contamination of this aquatic ecosystem and that further attention to this issue is warranted.     

Distribution patterns of polychlorinated dibenzo-p-dioxins and polychlorinated dibenzofurans in sediments of the Xiangjiang River, China

We investigated the occurrence and distribution patterns of 2,3,7,8-substituted polychlorinated dibenzo-p-dioxins and dibenzofurans (PCDD/Fs) in six sediment samples from the Xiangjiang River, Hunan Province, People’s Republic of China. Total concentrations of PCDD/Fs ranged from 876 to 497,759 (mean 160,766) ng/kg dw, the highest of which exceeded that have ever been reported for sediment samples. World Health Organization total toxicity equivalent (WHO-TEQ) concentrations in three out of six samples were significantly higher than the guidance level (21.5?ng WHO-TEQ/kg dw) suggested by Canadian Sediment Quality Guideline. A predominance of octachlorodibenzo-p-dioxin (OCDD) was observed with an average contribution of 90.8% to the total PCDD/F concentrations, while 1,2,3,4,6,7,8-heptachlorodibenzo-p-dioxin (HpCDD) was the major contributor to the PCDD/F WHO-TEQ concentrations in most of the sites. Such high levels of OCDD and HpCDD may be attributed to the presence of PCP/PCP-Na pollution, although MB-WW, agricultural straw open burning, and boilers–hazardous wastes were also the potential sources of PCDD/Fs. This is the first report for the concentrations and congener profiles of PCDD/Fs in sediment samples from the Xiangtan, Zhuzhou, and Changsha sections of the Xiangjiang River, providing scientific evidence for establishing priorities to reduce ecological risks posed by PCDD/Fs in the rapidly developing areas of Hunan Province and elsewhere.     

Monitoring dioxins and furans in the vicinity of an old municipal waste incinerator after pronounced reductions of the atmospheric emissions

In order to get an overall picture of the environmental impact of an old municipal solid waste incinerator (MSWI) from S. Adrià del Besòs (Barcelona, Catalonia, Spain), a monitoring program addressed at determining the levels of a number of pollutants in the vicinity of the facility was initiated in 1998. In March 1999, an adaptation was carried out due to EU legislation on pollutant emissions from the stack. As a result, emissions of polychlorinated dibenzo-p-dioxins (PCDDs) and dibenzofurans (PCDFs) were notably reduced, and a significant (30%) decrease was found in the levels of PCDD/F in herbage samples collected in the vicinity of the MSWI. In March 2001, herbage samples were collected at the same sampling points and the PCDD/F levels measured again. The current PCDD/F concentrations range from 0.23 to 1.43 ng I-TEQ kg(-1) (dry matter), with median and mean values of 0.58 and 0.66 ng I-TEQ kg(-1) (dry matter), respectively, while in the 2000 survey the PCDD/F concentrations ranged from 0.22 to 1.20 ng I-TEQ kg(-1) (dry matter), with median and mean values of 0.57 and 0.61 ng I-TEQ kg(-1) (dry matter), respectively. Although the current PCDD/F concentrations in herbage samples are comparable to those found in recent surveys carried out in various places of Catalonia, an exhaustive evaluation of the data, including principal component analysis, indicates that other emission sources of PCDD/Fs also have a notable environmental impact on the area under direct influence of the MSWI.     

钢铁厂及其周围土壤中二恶英和多氯联苯污染物的分布规律研究

利用同位素稀释高分辨气相色谱-高分辨质谱(HRGC/HRMS)的分析方法研究了东北某钢铁厂及其周围生活区、背景对照区土壤中二噁和多氯联苯污染物的污染水平和分布规律。结果表明,土壤中二噁的浓度和毒性当量分别为26pg/g(6.02～109pg/g)、0.72pg I-TEQ g-1(0.008～5.43pg I-TEQ g-1)。土壤中多氯联苯的浓度为955pg/g(268～3504pg/g),毒性当量值达0.07pg TEQ g-1(0.006～0.33pg TEQ g-1)。该区域土壤中的二噁和多氯联苯浓度明显低于一般国家居住地的土壤控制标准,处于较低的污染水平。     

Organochlorine contaminants in the Vistula Lagoon sedimentation zone as possible source of lagoon recontamination

The presented results include decade of monitoring of the Vistula Lagoon waters and have been supplemented by the determination of chlorinated compounds, as well as on concentrations of polychlorinated dibenzo-p-dioxins and dibenzofurans (PCDD/Fs) in the sedimentation zone. Monitoring of river waters entering the Polish part of the lagoon and the lagoon waters confirmed the presence of plant protection chemical; the largest contributors has lindane (34%) and DDT_total (21%); the same as for sediments were dominate lindane (19%) and DDT_total (14%) within pp-DDT isomer dominate (13%). In the lagoon water, PCDD/Fs were determined within a range of 1.5–5.6 ng dm^?3, leading to average toxicity of 0.18?±?0.13 ng TEQ·dm^?3. In sediments, their concentrations fell within a range of 22.7–405.7 ng kg^?1 dw and the average toxicity of the lagoon sediments was set at 5.00?±?1.98 ng TEQ·kg^?1 dw. Both in water and sediments, the greatest share among PCDD/Fs has octa-chlorodibenzodioxin. Due to the hydromorphological conditions of the lagoon, the waters are mixed to the bottom causing the surface layer of sediment to become remobilized—this is suggested as the key factor when it comes to water recontamination and increased access of POPs to marine organisms.     

Heavy metals and PCDD/Fs in solid waste incinerator fly ash in Zhejiang province,China: chemical and bio-analytical characterization

Fly ash samples were taken from solid waste incinerators with different feeding waste, furnace type, and air pollution control device in six cities of Zhejiang province. The solid waste incinerators there constitute one fifth of incinerators in China. Heavy metals and polychlorinated dibenzo-p-dioxins and dibenzofurans (PCDD/Fs) were analyzed in the fly ash. Moreover, the fly ash samples were extracted by toxicity characteristic leaching procedure (TCLP). The biotoxicity of the leachate was evaluated by Chlorella pyrenoidosa. High variation and contents were found for both the heavy metals and PCDD/Fs. The contents of Zn, Cu, As, Pb, Cd, Cr, Ni, and Hg in the fly ash samples varied from 300 to 32,100, 62.1–1175, 1.1–57, 61.6–620, 0.4–223, 16.6–4380, 1.2–94.7, and 0.03–1.4 μg g⁻¹ dw, respectively. The total contents of 17 PCDD/Fs varied from 0.1128 to 127.7939 μg g⁻¹ dw, and the 2,3,7,8-TeCDD toxic equivalents (TEQ) of PCDD/Fs ranged from 0.009 to 6.177 μg g⁻¹ dw. PCDF congeners were the main contributor to the TEQ. The leachate of the fly ash showed biotoxicity to C. pyrenoidosa. A significant correlation was found between the Cd and EC₅₀ values. Further research is required to investigate the environmental impact of the various pollutants in the fly ash.     

Temporal variation of PCDD/PCDF levels in environmental samples collected near an old municipal waste incinerator

In 1996 and 1997, the levels of polychlorinated dibenzo-p-dioxins (PCDDs) and dibenzofurans (PCDFs) were determined in soil and herbage samples taken from 24 sites in the vicinity of an old municipal solid waste incinerator (Montcada, Barcelona, Spain). To determine the temporal variation in the concentrations of PCDD/Fs, recently 24 soiland 24 herbage samples were again collected at the same sampling points and analyzed for PCDD/F levels. In the currentsurvey, PCDD/F concentrations in soils ranged between 0.06 and127 ng I-TEQ kg^-1 (dry matter), with median and mean values of 4.80 and 9.95 ng I-TEQ kg^-1 (dry matter), respectively. In turn, the levels of PCDD/Fs in herbage samples ranged from 0.40 to 1.94 ng I-TEQ kg^-1 (dry matter), with median and mean values of 0.86 and 0.95 ng I-TEQ kg^-1 (dry matter), respectively. The comparison with the data obtained in 1996 and 1997 show that while PCDD/F concentrations in herbage samples decreased substantially during the last two years, no significant differences in the levels of PCDD/Fs in soils were noted. On the other hand, the potential intake of polluted soils from the vicinity of the plant would not imply any significant health risk for the general population living in the area under influence of the facility.     

Concentrations of polychlorinated dibenzo-p-dioxins, dibenzofurans, non-ortho polychlorinated biphenyls, and mono-ortho polychlorinated biphenyls in Japanese flounder, with reference to the relationship between body length and concentration

The concentrations of polychlorinated dibenzo-p-dioxins (PCDDs), polychlorinated dibenzofurans (PCDFs), non-ortho polychlorinated biphenyls (non-ortho PCBs), and mono-ortho polychlorinated biphenyls (mono-ortho PCBs) in Japanese flounder (Paralichthys olivaceus, body length 10.4-36.6 cm) collected from Sendai Bay, Japan, were determined using high-resolution gas chromatography-mass spectrometry. The relationship between the concentrations of these compounds (dioxins) and the body length of the Japanese flounder was examined. The total PCDD and total PCDF concentrations did not correlate with body length (both r(2) < 0.1, both p > 0.05), whereas the total non-ortho PCB and total mono-ortho PCB (coplanar polychlorinated biphenyls, Co-PCBs) concentrations were significantly correlated (r(2)= 0.8, p < 0.05 and r(2)= 0.63, p < 0.05, respectively). The bioaccumulation properties of PCDD/Fs in Japanese flounder differed from those of Co-PCBs. Toxicity equivalency quotient (TEQ) values derived from the Co-PCBs made up 46.3%-63.7% of the total TEQ value for all the dioxins. Although the concentrations of non-ortho PCBs were lower than those of mono-ortho PCBs, the TEQ value for non-ortho PCBs was higher than that for mono-ortho PCBs. The TEQ value for non-ortho PCBs increased more with increasing body length than did the values for PCDDs, PCDFs, and mono-ortho PCBs. These results show that from the standpoint of risk management, non-ortho Co-PCBs are the most important of the dioxins in Japanese flounder.     

济南市大气细颗粒物中二(口恶)英污染水平及季节变化

2021年对济南市大气PM_2.5中17种2,3,7,8氯取代二(口恶)英(PCDD/Fs)污染现状进行监测。对其异构体分布、指示性单体、季节变化规律等特征及其与常规污染物相关性进行了分析。结果表明:大气PM_2.5中PCDD/Fs浓度范围和年平均值分别为0.157~1.595 pg/m³和0.785 pg/m³,而毒性当量(以I-TEQ计)范围和年平均值分别为0.009~0.116 pg TEQ/m³和0.052 pg TEQ/m³。PCDD/Fs浓度与毒性当量季节变化特征显著,均呈现出冬季>春季>秋季>夏季的情况,可能由季节性排放源和气象条件不同导致。不同季节PCDD/Fs异构体分布模式一致,主要由高氯代(1,2,3,4,6,7,8-HpCDF、OCDD、OCDF和1,2,3,4,6,7,8-HpCDD)单体组成;而对毒性当量贡献最大的单体是2,3,4,7,8-PeCDF,其与总毒性当量具有较好的相关性。同时,PCDD/Fs浓度与SO₂、NO₂、PM_2.5等大气常规污染物呈显著正相关。这表明,大气PM_2.5中PCDD/Fs与常规污染物的生成和排放密切相关。     

广州天河区大气中二噁英年度监测及气固分配规律

对广州天河区大气中二噁英进行年度监测和气固分配模式的研究。结果表明,天河区大气中存在较高浓度的二噁英;低氯代二噁英对毒性当量贡献较大,其主要分布在气相,2,3,4,7,8-PeCDF对毒性当量贡献最大,其贡献超过35%;高氯代二噁英(主要是OCDF、OCDD、1,2,3,4,6,7,8-HpCDF和1,2,3,4,6,7,8-HpCDD)对浓度贡献较大,其主要分布在颗粒相。     

The variability of PCDD/F concentrations in the effluent of wastewater treatment plants with regard to their hydrological environment

The occurrence, concentrations, patterns, and loads of 17 2,3,7,8-substituted congeners of polychlorinated dibenzo-p-dioxins (PCDDs) and polychlorinated dibenzofurans (PCDFs) were determined in treated wastewater collected at the outlets from 14 wastewater treatment plants (WTPs), divided into three size categories. The analysis also considered the effect of wastewater outflow on the final concentrations of PCDDs/Fs, as the samples were collected during flooding and stable hydrological conditions. None of the studied WTPs were found to completely remove toxic congeners of PCDDs/Fs from wastewater: the PCDD concentrations in the outgoing effluent during stable wastewater flow ranged from 2.99 to 177.19 pg/L, PCDFs from 6.05 to 51.30 pg/L, and the Toxic Equivalent (TEQ) was between 0.94 and 4.87 pg/L. The results from high wastewater flow were less diversified, ranging from 5.04 to 8.85 pg/L for PCDDs, from 11.47 to 32.33 pg/L for PCDFs and from 2.00 to 4.65 pg/L for TEQ. The smallest WTPs demonstrated the highest average total and TEQ concentrations due to limited volume, short retention time and outdated technology, and, hence, insufficient treatment efficiency. The largest WTPs have the potential to substantially affect the quality of river water, as despite being associated with the lowest concentrations, they released much greater volumes of treated wastewater and, hence, the greatest amounts of analyzed compounds. Elevated TEQ values were observed at high flow in all WTP size categories indicating the impact of high and stable wastewater flow on the concentrations of the observed PCDDs/Fs.     

Large variation in breast milk levels of organohalogenated compounds is dependent on mother's age, changes in body composition and exposures early in life

We identified factors that are important determinants of body burdens (breast milk levels) of polychlorinated biphenyls (PCBs), dioxins (polychlorinated dibenzo-p-dioxins (PCDDs) and polychlorinated dibenzofurans (PCDFs)) and polybrominated diphenyl ethers (PBDEs). PCBs, PCDD/Fs and PBDEs were analysed in breast milk from up to 325 first-time mothers in Uppsala, Sweden, who delivered between 1996 and 2006. Hierarchical clustering was used as a method for identification of groups of compounds with common sources of exposure and similar toxicokinetics. Based on correlations between levels of single compounds/congeners in breast milk, distinctly separated clusters were formed, strongly dependent on structural similarities of the organohalogen molecules. In a multiple regression model, levels of PCBs (except PCB 28), PCDD/Fs and BDE-153 were positively associated with age of the mother and weight loss after delivery and inversely associated with pre-pregnancy BMI (body mass index) and weight gain during pregnancy. Higher levels of mono-ortho PCB TEQ, non-ortho PCB TEQ and BDE-153 in milk were found among women with high physical activity. Women who were breastfed during infancy and grew up on the Baltic coast of Sweden, with high availability of contaminated fish from the Baltic sea, had higher levels of PCBs and PCDD/Fs in breast milk indicating that exposure early in life from breast milk and contaminated fish may still affect body burdens at the time of pregnancy. The importance of current consumption of fatty Baltic fish as a source of exposure was supported by the positive association with breast milk levels of mono-ortho PCB TEQ, PCDF TEQ and BDE-153. The results show that, in contrast to the lower brominated PBDE congeners, the hexa-brominated BDE-153 resembles the chlorinated compounds with regards to determinants in breast milk. This suggests that some of the PBDEs may have toxicokinetic properties and that are similar to the PCBs and PCDD/Fs. Our results show that a few simple advices to women regarding weight changes in connection with pregnancy and consumption of contaminated fatty fish during the whole lifetime may lower the levels of dioxins in breast milk by up to 60%.     

杭州城区环境空气中二口恶英浓度状况研究

依据2009年7月至2012年2月连续3年对杭州城区环境空气中二英（PCDD/Fs）采样分析结果得知，杭州城区环境空气中二英毒性当量质量浓度变化范围为0.13～0.55 pg TEQ/m³，均值为0.34 pg TEQ/m³。城区环境空气中二英浓度季节变化不显著，夏季略低于冬季；城区范围内不同功能区之间二英浓度差别不显著；连续3年监测结果未显现二英年度变化趋势。沙尘暴天气环境空气中二英浓度显著增高，日常天气和烟花爆竹集中燃放天气环境空气中二英形态分布存在明显区别，烟花爆竹集中燃放期间八氯代二苯并-对-二英（OCDD）占总质量浓度比例显著提高。利用IBM SPSS Statistics 19.0统计软件对24个监测结果聚类分析发现，杭州城区环境空气中二英的同类物分布具有明显的“源”分布特征。     

Pilot study of the polychlorinated dibenzo-p-dioxins and dibenzofurans level in agricultural soil in Shanghai, China

Polychlorinated dibenzo-p-dioxins and dibenzofurans (PCDD/Fs) were analyzed in agricultural soil samples from Shanghai to determine levels and to identify possible dioxin sources. The dioxin level was measured by an enzyme immunoassay method, US EPA 4025 (modified), which provides results as 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD) equivalents. The Method 4025m results obtained from 60 soil samples displayed a normal distribution, ranging from 2.8 to 23.4 pg/g 2378-TCDD-equvalents, with an average of 11.0 pg/g. The result also revealed a similar PCDD/Fs concentration among crop usage patterns, but differences by geographic region, low in the southwest of Shanghai and considerably higher in the northwest region. In contrast, the dioxin concentrations on Chongming Island were fairly homogeneous, with a range 10–15 pg/g. This immunoassay method is an effective high throughput screening tool which helps to minimize the need for more expensive analyses.     

Characteristic occurrence patterns of micropollutants and their removal efficiencies in industrial wastewater treatment plants

The concentrations and removal efficiencies of various kinds of micropollutants were investigated and the relationships between the input sources of industrial wastewater and occurrence patterns of each micropollutant were identified at nine on-site industrial wastewater treatment plants (WWTPs). The distribution pattern of each compound varied according to the WWTP type and several micropollutants were significantly related with specific industries: chlorinated phenols (ClPhs) with paper and metal industries, polycyclic aromatic hydrocarbons (PAHs) with petrogenic- and pyrogenic-related industries, polychlorinated dibenzo-p-dioxins and dibenzofurans (PCDD/Fs) with the paper industry, and chlorinated benzenes (ClBzs) with dye-related industries. The activated sludge (AS) process was very efficient in the removal of ClPhs and PAHs, and the filtration process in the removal of PCDD/Fs and 1,4-dioxane. Generally, the removal efficiencies of each micropollutant varied according to the WWTP type.