官厅水库沉积物表层中的有机氯农药分布特征及风险评价

采用气相色谱法对北京市官厅水库沉积物表层中持久性有机氯农药(OCPs)的残留状况进行了调查,并对有机氯农药污染水平和生态风险作出评价。结果表明:沉积物中有机氯农药总含量为8.48 ng/g～24.40 ng/g,其中HCHs和DDTs的含量较高,分别为1.11 ng/g～7.73 ng/g和2.97 ng/g～10.52 ng/g,其组分特征为来自环境的残留。与沉积物风险评估低值(ERL)和风险评估中值(ERM)对比评价沉积物中有机污染物的风险程度,官厅水库沉积物表层中的有机氯农药存在一定的生态风险。     

山美水库流域表层沉积物中DDTs农药的残留特征及风险评估

利用GC-ECD检测了山美水库流域表层沉积物中DDTs农药含量,分析了其残留与组成特征及生态风险.结果表明,表层沉积物中DDTs平均含量为4.07 ng/g,其含量范围为0.96～8.20 ng/g;DDTs含量大小顺序为桃溪与湖洋溪汇流(8.20 ng/g)>湖洋溪(4.67 ng/g)>桃溪(4.59 ng/g)>山美水库(1.96 ng/g).表层沉积物中新的DDTs输入量比较少;沉积物中DDTs主要来自于早期残留或是施用农药长期风化后的土壤;大多数采样点DDTs发生好氧生物降解,降解产物以DDE为主.对照Ingersoll风险评估标准,表层沉积物中DDTs农药残留具有较高的生态风险.     

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。     

微波消解-原子荧光光谱法测定大气PM2.5中的砷

采用微波消解-原子荧光光谱法测定大气细颗粒物中的砷，确定了最佳样品处理方法与测定条件。方法在0μg/L～40．0μg/L范围内线性良好，标准曲线相关系数达0．999以上，检出限为0．01μg/L。土壤标准品的测定值在标准值范围内，大气PM2．5滤膜样品加标回收率为96．0％～102％，5次平行测定的RSD为1．5％～3．6％。     

超高效液相色谱-串联质谱法分析土壤及沉积物中氨基甲酸酯农药

利用超高效液相色谱-串联质谱,建立土壤和沉积物中痕量氨基甲酸酯农药的分析方法。该方法用体积比1:1的二氯甲烷/甲醇对土壤和沉积物样品进行加速溶剂萃取,GCB/PSA固相萃取小柱对萃取液进行净化,内标法定量,用超高效液相色谱-串联质谱法分析土壤和沉积物中20种氨基甲酸酯农药。20种氨基甲酸酯农药在0.02~1.0 μg/mL范围内线性良好(r≥0.99),检测限为0.20~0.60 ng/g。沉积物加标样品(20ng/g)和土壤加标样品(20ng/g)的回收率分别为33.2%~101.9%、38.8%~120.5%,相对标准偏差为6.1%~28.0%、2.3%~16.0%。沉积物加标样品(2.0 ng/g)回收率为43.0%~100.0%,相对标准偏差为2.1%~11.3%。     

厦门西海域拟疏浚物中多氯联苯含量分布及生态风险评价

对厦门西海域拟疏浚物中的PCBs含量及分布特征进行了调查，结果表明，厦门西海域拟疏浚物中PCBs为0．17ng／g-30．3ng／g，其中马銮湾2个站位PCBs的总含量高于《海洋沉积物质量》（GB18668—2002）一类标准值。生态风险评价结果显示厦门西海域拟疏浚物中多氯联苯的环境毒性相对较低。     

广州大学城珠江水域多环芳烃的污染特征

利用GC-MS对广州大学城珠江水域的地表水及表层沉积物中多环芳烃(PAHs)的含量进行了分析。结果表明,广州大学城珠江水域及表层沉积物中均可检出PAHs,水体优控PAHs总量在1061.7~6577.8ng/L之间,沉积物中优控PAHs总量分布在896.1~7248ng/g之间。广州大学城珠江水域的PAHs属混合来源,主要有石油类产品的输入(漏油泄油)和化石燃料的燃烧(大气沉降)。     

中国表层水体沉积物中多环芳烃源解析及评价

采用索氏提取气相色谱-质谱法测定中国6个重点水体表层沉积物中16种多环芳烃的含量。各化合物含量范围分别为长江6.20~163 ng/g、淮河7.90~249 ng/g、海河12.1~401 ng/g、松花江5.75~152 ng/g、太湖29.1~2 810 ng/g和滇池19.1~795ng/g；16种多环芳烃的总量分别为：长江1 147 ng/g、淮河1 723 ng/g、海河2 595 ng/g、松花江793 ng/g、太湖12472 ng/g、滇池3 714 ng/g，属中等污染水平。利用特征分子比值法分析结果表明6条水体表层沉积物中PAHs均可能以燃料（包括柴油、汽油、煤、木材）燃烧以及焦化污染为主。淮河和滇池还可能存在轻微石油泄漏污染。利用沉积物质量基准法（SQGs）和沉积物质量标准法分别对6条水体表层沉积物中多环芳烃的风险评估表明严重的多环芳烃生态风险在这些水体表层沉积物中不存在，但长江、淮河、松花江、海河均可能存在一定的潜在风险，负面生物毒性效应会偶尔发生，风险主要来源于荧蒽和菲。太湖和滇池水体中存在的潜在多环芳烃风险种类较多，风险主要来源于菲、荧蒽、芘、苯并（a）蒽、苊和蒽，对水生生物毒性效应较高，有必要进行更深入细致的调查研究高风险区域底栖生物的受损状况、污染来源和途径，以制定合理的污染控制对策。     

液相色谱-串联质谱法测定水体、沉积物及土壤中全氟化合物

建立了水、沉积物及土壤中13种全氟化合物(PFCs)的富集、净化、浓缩的前处理方法及快速液相色谱三重四级杆串联质谱的分析方法。9种全氟羧酸、2种典型全氟磺酸、2种磺酰铵衍生前体物的响应因子与质量浓度的线性关系良好。添加回收实验表明,13种全氟化合物在水、土壤和沉积物中的回收率为52.3%~119.3%,变异系数为2.3%~19.4%,方法检出限分别为0.015~0.472 ng/L、0.012~0.875 ng/g、0.004~0.743 ng/g。该法成功应用于实际样品的测定,沉积物和土壤中分别检测到3种和10种全氟化合物。     

微波消解石墨炉原子吸收法测定土壤和沉积物中的铍

以氯化钯为基体改进剂，采用微波消解石墨炉原子吸收法测定土壤和沉积物中的铍，优化了微波消解条件，考察了共存元素对测定的干扰。方法在0μg／L～4．00μg／L范围内线性良好，检出限为0．01μg／g（以取样质量0．2000g、定容体积50mL计），标准样品平行测定的RSD为3．5％～6．7％，实际样品的加标回收率为84．0％-113％。     

Analysis and occurrence of emerging chlorinated and brominated flame retardants in surficial sediment of the Dalian coastal area in China

The concentrations and distributions of some typical chlorinated flame retardants (Dechlorane or Mirex, Dechlorane 602 (Dec 602), Dechlorane 603 (Dec 603), Dechlorane 604 (Dec 604) and Dechlorane Plus (DP)) and brominated FRs (polybrominated diphenyl ethers (PBDEs), pentabromoethylbenzene (PBEB) and 1,2-bis(2,4,6-tribromophenoxy)ethane (BTBPE)) were analyzed in surficial sediment collected from the Dalian coastal area in northeast China. Dec 603, Dec 604, and BTBPE were below their respective limits of detection (LOD) in all sediment samples, while Dechlorane, Dec 602, DP, Σ13BDE (tri- to hepta-BDEs), BDE 209, and PBEB were identified in the ranges <0.015-39.9 ng g(-1) dry weight (dw), <0.011-0.156 ng g(-1) dw, 0.69-7.00 ng g(-1) dw, 0.017-1.33 ng g(-1) dw, 3.94-103 ng g(-1) dw, and <0.073-1.9 ng g(-1) dw, respectively. Relationships between these chlorinated and brominated FRs were analyzed using Pearson's correlation and principal component analysis (PCA). DP, Dechlorane, Σ13BDE, and BDE 209 showed significantly positive correlation (p<0.05), and these relationships showed excellent agreement with PCA results. The spatial trends for Dechlorane, DP, BDE 209, and Σ13BDE showed that high concentrations were found in the industrial zone and lower concentrations in residential and garden zones. The results imply that these FRs are originating from a common source, and support the view that direct input from the effluent of sewage outlets is a major source of these compounds in Dalian sediment.     

Short-range transport of contaminants released from e-waste recycling site in South China

The transport behaviors of a suite of contaminants released from electronic waste (e-waste) recycling operations, including polybrominated diphenyl ethers (PBDEs), polychlorinated biphenyls (PCBs), and heavy metals, were evaluated by analyzing the contaminant residues in surface soils sampled in the surrounding area of an e-waste recycling site in South China. Concentrations of PBDEs and PCBs in the soil samples ranged from 0.565 to 2908 ng g(-1) dw and from 0.267 to 1891 ng g(-1) dw, respectively, while soil residues were 0.082-2.56, 3.22-287, and 16.3-162 μg g(-1) dw for Cd, Cu, and Pb, respectively. Concentrations of PBDEs and PCBs in soil decreased with increasing distance from the source of pollution, indicating possible PBDE and PCB contamination in the surrounding areas due to the short-range transport of these compounds from the e-waste recycling site. Although no significant difference in the short-range transport potential among PBDE and PCB congeners was observed, reductions in concentrations of the highly-brominated-BDEs and highly-chlorinated-CBs were slightly quicker than those of their less-halogen-substituted counterparts. Conversely, heavy metals showed the lowest transport potential due to their low vapor pressure, and results showed metals would remain near the pollution source instead of diffusing into the surrounding areas. Finally, mass inventories in areas near the e-waste site were 0.920, 0.134, 0.860, 4.68, 757, and 673 tons for BDE209, PBDEs (excluding BDE209), PCBs, Cd, Cu, and Pb, respectively.     

Profiles,sources, and transport of polycyclic aromatic hydrocarbons in soils affected by electronic waste recycling in Longtang,south China

We studied the profiles, possible sources, and transport of polycyclic aromatic hydrocarbons (PAHs) in soils from the Longtang area, which is an electronic waste (e-waste) recycling center in south China. The sum of 16 PAH concentrations ranged from 25 to 4,300 ng/g (dry weight basis) in the following order: pond sediment sites (77 ng/g), vegetable fields (129 ng/g), paddy fields (180 ng/g), wastelands (258 ng/g), dismantling sites (678 ng/g), and former open burning sites (2,340 ng/g). Naphthalene, phenanthrene, fluoranthene, pyrene, chrysene, and benzo[b]fluoranthene were the dominant PAHs and accounted for approximately 75 % of the total PAHs. The similar composition characteristics of PAHs and the significant correlations among individual, low molecular weight, high molecular weight, and total PAHs were found in all six sampling site types, thus indicating that PAHs originated from similar sources. The results of both isomeric ratios and principal component analyses confirmed that PAHs were mainly derived from the incomplete combustion of e-waste. The former open burning sites and dismantling sites were the main sources of PAHs. Soil samples that were taken closer to the point sources had high PAH concentrations. PAHs are transported via different soil profiles, including those in agricultural fields, and have been detected not only in 0- to 40-cm-deep soil but also in 40 cm to 80 cm-deep soil. PAH concentrations in soils in Longtang have been strongly affected by primitive e-waste recycling, particularly by former open burning activities.     

Distribution and partitioning of aliphatic hydrocarbons and polycyclic aromatic hydrocarbons between water, suspended particulate matter, and sediment in harbours of the West coastal of the Gulf of Tunis (Tunisia)

Harbours of La Goulette, Rades and Sidi Bou Said are considered as the principal largest and most important port in the Gulf of Tunis characterised by a direct influence of different activities (sailing, industry and fishing) to the Mediterranean Sea. Due to their social and economic impact, a comprehensive assessment of the spatial distribution and partitioning of 24 polycyclic aromatic hydrocarbons (PAHs) and 18 aliphatic hydrocarbons (AHs) in summer and in winter among overlying water, suspended particulate matter (SPM) and surface sediments is essential. Distribution of hydrophobic organic contaminants in abiotic compartments is important for describing their transfer and fate in aquatic ecosystems and to identify the potential danger due to mobilization of contaminants produced by managing of the same sediments. Total organic carbon (TOC) contents range between 4.3% and 6.5%, with an average value of 5.9% in summer, and between 2.3% and 9.6%, with an average value of 6.1% in winter. The average concentrations of ΣPAH in winter and in summer were respectively 703.1 ng L?1 and 378.4 ng L?1 in seawater, 4599.1 ng g?1 and 3114 ng g?1 in SPM, and 1507.6 ng g?1 dw (dry weight) and 1294.6 ng g?1 dw in surface sediment. For ΣAH the average concentrations in winter and in summer were respectively 701 ng L?1 and 741.7 ng L?1 in seawater, 6743.5 ng g?1 and 6282.9 ng g?1 in SPM, and 4971.3 ng g?1 and 4588.1 ng g?1 in surface sediment. Higher PAH and AH concentrations were observed in SPM than in surface sediment. SPM and water were dominated by PAH with low molecular weight, while for sediment low and high molecular weight PAHs were present. PAH and AH fingerprint ratios, such as pristane to phytane (Pr/Ph), phenanthrene to anthracene (Phe/An) and fluoranthene to pyrene (Fl/Py), suggest that hydrocarbons in all harbours may originate from both pyrolytic and petrogenic sources derived from discharge of untreated sewage and wastewater or from direct input by ship traffic in the area. The results showed significant difference (ANOVA, p < 0.05) for hydrocarbon mean concentrations between all harbours studied and between different matrixes.     

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.     

Quantitative analyses of selected polychlorinated biphenyl (PCB) congeners in water,soil, and sediment during winter and spring seasons from Msunduzi River,South Africa

The lack of information and the need for knowledge on the organic pollutants within the area of KwaZulu-Natal together with the global problem of water supply have prompted our investigation into the analyses of eight polychlorinated biphenyl (PCB) congeners in the Msunduzi River of KwaZulu-Natal, South Africa. Soil, sediment, and water samples were collected at ten different sites along the river during winter and spring seasons. Soil and sediment samples were extracted using ultra sonication with dichloromethane while water samples were liquid-liquid extracted using dichloromethane. All sample extracts were cleaned-up using a multi-layer silica gel column and analyzed with gas chromatography-mass spectrometry. Quality assurance measures were also determined. The percentage recoveries for water were 53–128 for all the PCBs analyzed, while sediment recoveries ranged between 69 and 105%. The highest total concentrations of the PCBs in sediment were 214.21–610.45 ng/g dw at the Du Toit sampling site and 30.86–444.43 ng/g dw basis at the wastewater treatment inlet for winter and spring, respectively. Soil PCB concentrations were 76.53–397.75 ng/g dw at the Msunduzi Town sampling site and 20.84–443.49 ng/g (dry weight) at the Du Toit sampling site for winter and spring, respectively. In addition, high PCB concentrations were found in effluent of the wastewater treatment inlet compared to other sampling sites, which ranged between 0.68–22.37 and 2.53–35.69 ng/mL for winter and spring seasons, respectively. In all the sampling sites selected for this study, Du Toit afforded the highest PCB concentration levels and the lowest was after chlorination at the Darvill wastewater treatment plant. The results presented are new and it is the first study of organic pollutants such as PCBs that has been carried out on this river.     

Chemometrics in assessment of seasonal variation of water quality in fresh water systems

The spatial and temporal distribution of polycyclic aromatic hydrocarbons (PAHs) was investigated in Gomti River, a major tributary of the Ganga river (India). A total of 96 samples (water and sediments) were collected from eight different sites over a period of 2 years and analysed for 16 PAHs. The total concentrations of 16 PAHs in water and bed sediments ranged between 0.06 and 84.21 ??g/L (average (n?=?48), 10.33 ± 19.94 ??g/L) and 5.24?C3,722.87 ng/g dw [average (n?=?48): 697.25 ± 1,005.23 ng/g dw], respectively. In water, two- and three-ring PAHs and, in sediments, the three- and four-ring PAHs were the dominant species. The ratios of anthracene (An)/An + phenenthrene and fluoranthene (Fla)/Fla + pyrene were calculated to evaluate the possible sources of PAHs. These ratios reflected a pattern of pyrolytic input as a major source of PAHs in the river. Principal component analysis, further, separated the PAHs sources in the river sediments, suggesting that both the pyrolytic and petrogenic sources are contributing to the PAHs burden. The threat to biota of the river due to PAHs contamination was assessed using effect range low and effect range median values, and the results suggested that sediment at some occasions may pose biological impairment.     

Polycyclic aromatic hydrocarbons in water, sediment and soil of the Songhua River Basin, China

The Songhua River is the third largest river in China and the primary source of drinking and irrigation water for northeastern China. The distribution of 16 priority polycyclic aromatic hydrocarbons (PAHs) in water [dissolved water (DW) and suspended particulate matter (SPM)], sediment, and soil in the river basin was investigated, and the associated risk of cancer from these PAHs was also assessed. The total concentration of PAHs ranged from 13.9 to 161 ng L^?1 in DW, 9.21 to 83.1 ng L^?1 in SPM, 20.5 to 632 ng g^?1 dw (dry weight) in sediment, and from 30.1 to 870 ng g^?1 dw in soil. The compositional pattern of PAHs indicated that three-ring PAHs were predominant in DW and SPM samples, while four-ring PAHs dominated in sediment and soil samples. The spatial distribution of PAHs revealed some site-specific sources along the river, with principal component analysis indicating that these were from pyrogenic sources (such as coal and biomass combustion, and vehicle emissions) and coke oven emission distinguished as the main source of PAHs in the Songhua River Basin. Based on the ingestion of PAH-contaminated drinking water from the Songhua River, cancer risk was quantitatively estimated by combining the Incremental Lifetime Cancer Risk assessment model and BaP-equivalent concentration for five age groups of people (adults, teenagers, children, toddlers, and infants). Overall, the results suggest that the estimated integrated lifetime cancer risk for all groups was in acceptable levels. This study is the first attempt to provide information on the cancer risk of PAHs in drinking water from the Songhua River.     

Chlorinated and brominated dibenzo-p-dioxins and dibenzofurans in surface sediment from Taihu Lake, China

Polychlorinated dibenzo-p-dioxins and dibenzofurans (PCDD/Fs) and polybrominated dibenzo-p-dioxins and dibenzofurans (PBDD/Fs) in surface sediment samples from Taihu Lake--an important water supply of the Yangtze River Delta, China--were investigated in the present study. Concentrations of PCDD/Fs ranged from 0.91 to 4.8 pg TEQ g(-1) dw (mean: 2.9 pg TEQ g(-1) dw, TEQ: Toxic Equivalent), which were all higher than the threshold effect level established by interim sediment quality guidelines in Canada (0.85 pg TEQ g(-1) dw). The levels of PBDD/Fs ranged from 0.16 to 1.6 pg TEQ g(-1) dw (mean: 0.52 pg TEQ g(-1) dw) and accounted for 5-33% (mean: 14%) of the total PCDD/Fs and PBDD/Fs TEQ. Comparatively, the abundance of sedimentary PCDD/Fs in the three regions (Meiliang Bay, Gonghu Bay, and Xukou Bay) showed a decreasing trend from the inflow region to the outflow region, while no significant difference was observed among their 2,3,7,8-PBDD/Fs levels, which suggested that the sources of PCDD/Fs and PBDD/Fs differed in this area. Principal component analysis suggested that the historical production/usage of pentachlorophenol and sodium pentachlorophenate was the dominant source of PCDD/Fs in the sediment of these regions. Although the specific sources of PBDD/Fs in the sediment of Taihu Lake were unclear, it was suspected to be due to atmospheric deposition; however, an additional study is needed to confirm this.     

珠江三角洲城市群及高海拔地区表层土中有机氯农药的空间分布特征

利用GC-ECD方法测定了珠江三角洲城市群及高海拔地区表层土壤中的有机氯农药。有机氯农药变幅为2.4~78.7 ng/g,平均15.9 ng/g。最高值出现在江门。总HCHs变幅为ND~19.2 ng/g,平均2.91 ng/g, 最高值出现在佛山。总DDTs变幅为ND~74.6 ng/g,平均值为9.91 ng/g。最高值出现在东莞。六氯苯在佛山较高。灭蚁灵在深圳的污染较其它地区严重。总体来说,HCHs污染程度较低,但部分地区有林丹的使用;有些采样点DDTs的污染程度超过了国家土壤环境质量标准的一级自然背景值,且有些区域可能有非三氯杀螨醇的DDTs外源输入。