Distribution,seasonal variation and inhalation risks of polychlorinated dibenzo-<Emphasis Type="Italic">p</Emphasis>-dioxins and dibenzofurans,polychlorinated biphenyls and polybrominated diphenyl ethers in the atmosphere of Beijing,China

Spatial distribution, seasonal variation and potential inhalation risks of polychlorinated dibenzo-p-dioxins and dibenzofurans (PCDD/Fs), polychlorinated biphenyls (PCBs) and polybrominated diphenyl ethers (PBDEs) were investigated in the atmosphere of Beijing, using passive air samplers equipped with polyurethane foam disks. Concentrations of ΣPCDD/Fs, ΣPCBs and ΣPBDEs ranged from 8.4 to 179 fg WHO₂₀₀₅-TEQ/m³, 38.6–139 and 1.5–176 pg/m³, respectively. PCDFs showed higher air concentrations than those of PCDDs, indicating the influence of industrial activities and other combustion processes. The non-Aroclor congener, PCB-11, was detected in air (12.3–99.4 pg/m³) and dominated the PCB congener profiles (61.7–71.5% to ∑PCBs). The congener patterns of PBDEs showed signatures from both penta-BDE and octa-BDE products. Levels of PCDD/Fs, PCBs and PBDEs at the industrial and residential sites were higher than those at rural site, indicating human activities in urban area as potential sources. Higher air concentrations of PCDD/Fs, PCBs and PBDEs were observed in summer, which could be associated with atmospheric deposition process, re-volatilization from soil surface and volatilization from use of technical products, respectively. Results of inhalation exposure and cancer risk showed that atmospheric PCDD/Fs, dioxin-like PCBs and PBDEs did not cause high risks to the local residents of Beijing. This study provides further aid in evaluating emission sources, influencing factors and potential inhalation risks of the persistent organic pollutants to human health in mega-cities of China.     

Reviewing the relevance of dioxin and PCB sources for food from animal origin and the need for their inventory,control and management

Background

In the past, cases of PCDD/F and PCB contamination exceeding limits in food from animal origin (eggs, meat or milk) were mainly caused by industrially produced feed. But in the last decade, exceedances of EU limit values were discovered more frequently for PCDD/Fs or dioxin-like(dl)-PCBs from free range chicken, sheep, and beef, often in the absence of any known contamination source.

Results

The German Environment Agency initiated a project to elucidate the entry of PCBs and PCDD/Fs in food related to environmental contamination. This paper summarizes the most important findings. Food products from farm animals sensitive to dioxin/PCB exposure—suckling calves and laying hens housed outdoor—can exceed EU maximum levels at soil concentrations that have previously been considered as safe. Maximum permitted levels can already be exceeded in beef/veal when soil is contaminated around 5 ng PCB-TEQ/kg dry matter (dm). For eggs/broiler, this can occur at a concentration of PCDD/Fs in soil below 5 ng PCDD/F–PCB-TEQ/kg dm. Egg consumers—especially young children—can easily exceed health-based guidance values (TDI). The soil–chicken egg exposure pathway is probably the most sensitive route for human exposure to both dl-PCBs and PCDD/Fs from soil and needs to be considered for soil guidelines. The study also found that calves from suckler cow herds are most prone to the impacts of dl-PCB contamination due to the excretion/accumulation via milk. PCB (and PCDD/F) intake for free-range cattle stems from feed and soil. Daily dl-PCB intake for suckler cow herds must in average be less than 2 ng PCB-TEQ/day. This translates to a maximum concentration in grass of 0.2 ng PCB-TEQ/kg dm which is less than 1/6 of the current EU maximum permitted level. This review compiles sources for PCDD/Fs and PCBs relevant to environmental contamination in respect to food safety. It also includes considerations on assessment of emerging POPs.

Conclusions

The major sources of PCDD/F and dl-PCB contamination of food of animal origin in Germany are (1) soils contaminated from past PCB and PCDD/F releases; (2) PCBs emitted from buildings and constructions; (3) PCBs present at farms. Impacted areas need to be assessed with respect to potential contamination of food-producing animals. Livestock management techniques can reduce exposure to PCDD/Fs and PCBs. Further research and regulatory action are needed to overcome gaps. Control and reduction measures are recommended for emission sources and new listed and emerging POPs to ensure food safety.

     

Distribution of polychlorinated dibenzo-p-dioxins,polychlorinated dibenzofurans,dioxin-like polychlorinated biphenyl and polycyclic aromatic hydrocarbons in the sediment of Temsah lake,Suez Canal,Egypt

Lake Temsah is one of the main wetlands in the Suez Canal region, and the main source for fish for the area. The lake is the end-point of several wastewater effluents. In the present study, residues of polychlorinated dibenzo-p-dioxins (PCDDs) and polychlorinated dibenzofurans (PCDFs), dioxin-like polychlorinated biphenyl (PCB) and polycyclic aromatic hydrocarbons (PAH) were monitored in the sediment of the lake. Samples were collected from six different sampling stations around the lake using a box-corer sampler, then kept frozen. Samples were extracted and cleaned up before residue determination was conducted using an HRGC/HRMS. An HP 6890 plus gas chromatograph was coupled to a Micromass Autospec Ultima mass spectrometer operating in EI mode at 35 eV and with a resolution of 10.000 (5% valley). PCDDs and PCDFs were detected in all sediment samples collected from various sampling stations. Results showed some progressive increase in PCDDs concentrations relevant to increase in chlorination. In the PCDD group of congeners, 1, 2, 3, 4, 6, 7, 8, 9 octa-CDD had the highest detected concentrations in all samples, while 2, 3, 7, 8 tetra-CDD showed the lowest concentrations. The World Health Organization toxicity equivalents ranged from 0.387 to 11.20 ng kg^?1 d.w. For PCDD homologues, hexa-CDD was the most dominant homologue in all sediment samples analysed. Regarding dioxin-like PCBs, results showed that IUPAC No. 118 congener, 2, 3, 4, 4, 5, pentachlorobiphenyl was the most concentrated of all detected congeners, with concentrations ranging between 0.039 and 43.201 µg kg^?1. For polycyclic aromatic hydrocarbons, benzo(b+k+j)fluoranthene had the highest concentrations in almost all sampling stations. However, fluorene was the smallest detected concentration in almost all stations. This result would indicate that PAH contamination of the lake seems to be coming from one main source in all sampling stations. The present work is the first record of PCCDs, PCCFs, and dioxin-like PCBs in the Temsah lake. The concentrations of the contaminants monitored in this study, especially those of PAHs, are rather alarming. Efforts should be made to stop point sources that contaminate the lake.     

不同垃圾焚烧炉产生的PCDD/Fs和PCBs同类物的分布

要应用高分辨气相色谱一质谱联用技术，测定了3种垃圾焚烧炉产生的飞灰中17种PCDD／Fs和12种共平面PCBs的浓度及毒性当量，比较了PCDD／Fs和PCBs同类物分布的差异．结果表明，流化床焚烧炉和炉排焚烧炉产生的PCDD／Fs多于PCBs，而气化熔融焚烧炉产生的PCBs多于PCDD／Fs；产生的PCBs对总毒性当量的贡献都比较小；3种焚烧炉产生的PCDD／Fs同类物具有相似的浓度分布；流化床焚烧炉和炉排焚烧炉产生的PCBs同类物具有相似的浓度分布，而气化熔融焚烧炉产生的PCBs同类物分布与其他两种焚烧炉差别较大．     

The Distribution and Impacts of Dioxins and Polychlorinated Biphenyls in the Taiwan Er-Jen River

Abstract

The distribution and impacts of polychlorinated dibenzo-p-dioxins and dibenzofurans (PCDD/DFs) and polychlorinated biphenyls (PCBs) in the Taiwan Er-Jen River were investigated by monitoring fish distribution and measuring PCDD/DFs and PCBs levels in sediment and fish samples. Most of the fish collected are pollution-resistant species such as Oreochromis spp, Liza macrolepsis, Channa spp and Megalops cyprinoides. the most polluted river sections are in the upstream where large amount of waste effluents from households, livestock rearing and nearby dumping sites were discharged into the river, and the lower reaches of the river where metal recovery activities including open burning of waste electrical wire/scrap occurred. Sediment samples collected near the burning site show 2,3,7,8-TCDD toxicity equivalents (TEQ) ranging from 0.014 to 14.2 ng g^?1 by PCDD/DFs and from 0.015 to 1.03 ng g^?1 by coplanar PCBs (Co-PCBs). the fish samples show TEQ ranging from 0.029 to 0.615 ng g^?1 by PCDD/DFs and from 0.012 to 0.12 ng g^?1 by Co-PCBs. Possible PCDD/DFs sources are discharged PCBs, open burning of waste wire/scrap, and pentachlorophenol. the consumption of these fish will cause an average intake of 54 pg kg^?1 d^?1 TEQ. the prevention of direct discharge of livestock and the dumping of waste effuents into River Er-Jen as well as the control of metal recovery activities appears to be the first step toward the restoration of River Er-Jen.     

Organochlorines in urban soils from Central India: probabilistic health hazard and risk implications to human population

This study presents distribution of organochlorines (OCs) including HCH, DDT and PCBs in urban soils, and their environmental and human health risk. Forty-eight soil samples were extracted using ultrasonication, cleaned with modified silica gel chromatography and analyzed by GC-ECD. The observed concentrations of ∑HCH, ∑DDT and ∑PCBs in soils ranged between?<?0.01–2.54, 1.30–27.41 and?<?0.01–62.8 µg kg^?1, respectively, which were lower than the recommended soil quality guidelines. Human health risk was estimated following recommended guidelines. Lifetime average daily dose (LADD), non-cancer risk or hazard quotient (HQ) and incremental lifetime cancer risk (ILCR) for humans due to individual and total OCs were estimated and presented. Estimated LADD were lower than acceptable daily intake and reference dose. Human health risk estimates were lower than safe limit of non-cancer risk (HQ?<?1.0) and the acceptable distribution range of ILCR (10^?6–10^?4). Therefore, this study concluded that present levels of OCs (HCH, DDT and PCBs) in studied soils were low, and subsequently posed low health risk to human population in the study area.     

Contamination and source assessment of metals,polychlorinated biphenyls,and polycyclic aromatic hydrocarbons in urban soils from Addis Ababa,Ethiopia

Urban areas in developing countries are facing vast environmental problems as a result of rapid urbanization and industrialization. Of major concern is the contamination of soils which are increasingly becoming sinks for environmental pollutants. However, to date only little is known about the pollution in the megalopolises of developing countries. The aim of this study was to assess the contamination and potential sources of metals, polychlorinated biphenyls (PCBs) and polycyclic aromatic hydrocarbons (PAHs) in the urban environment of Addis Ababa, the capital of Ethiopia. The investigation revealed the presence of most of the analyzed pollutants in soil and sediment samples with total concentrations (dry wt) of PAHs ranging from 186 to 3150?µg?kg^?1, PCBs from 0.4 to 19?µg?kg^?1, Cu from 14 to 173?mg?kg^?1, Zn from 36 to 440?mg?kg^?1, Pb from 9 to 700?mg?kg^?1, and Ni from 16 to 72?mg?kg^?1. In addition, polyaromatic sulfur heterocycles, typical for oil and petrol residues, were detected in several soil samples. Source identification approaches revealed that Pb, Zn, and Cu are most likely derived from pyrolytic sources, with elevated values in samples related to waste combustion and traffic emissions. Ni is most probably of geogenic origin. For PCBs it is indicated that they are derived from a single source. However, correlations with technical PCB mixtures were inconsistent. PAHs originate from the combustion of biomass, vehicular exhausts, and petrogenic sources.     

环境多介质中PCDD/Fs人群健康风险评价——以珠江三角洲为例

基于珠江三角洲不同环境介质（水体、大气和土壤）及食物中PCDD/Fs的研究资料,利用VLIER-HUMAAN模型评估了该区域不同暴露途径下PCDD/Fs对人群潜在健康风险。结果表明：珠江三角洲地区人群平均每日摄入PCDD/Fs的量（TDI）为3.312 pg WHO1998-TEQ/kg·d-1,低于世界卫生组织（WHO）组织推荐的容许标准（4 pg WHO1998-TEQ/kg·d-1）。从暴露途径来看,珠江三角洲地区成年人摄入PCDD/Fs的主要途径食物摄取,约占了98.0%。在食物暴露中,水产品是主要途径,约占总摄入量的70%,蔬菜和肉蛋类分别占了16.6%和10.5%,其它较低。水产品是PCDD/Fs引起人群健康风险的重要风险源,应采取有效措施保障水产品质量,同时,调整饮食结构,降低PCDD/Fs暴露的潜在风险。     

Spatial distribution of polychlorinated dibenzo-p-dioxins and polychlorinated dibenzofurans in soil around a municipal solid waste incinerator

Municipal solid waste incinerators (MSWIs) are usually considered to be important sources of polychlorinated dibenzo-p-dioxins and polychlorinated dibenzofurans (PCDD/Fs). To examine the influence of PCDD/Fs emissions from a MSWI on the surrounding environment, 21 soil samples were collected from various sampling sites distributed at distances of 300–1,700 m away from the stack of a MSWI. International Toxic Equivalent (I-TEQ) concentrations ranged from 0.47 to 2.07 pg I-TEQ g^?1, with average and median concentrations of 1.08 and 1.05 pg I-TEQ g^?1, respectively. Comparison of the results presented herein with other worldwide studies suggested that the concentrations of PCDD/Fs in the ambient soil were relatively low, indicating a limited impact on the surrounding environment. The emission concentrations from the incinerator were the critical factor in generating an environmental impact on the surrounding environment. An exponential function was developed, indicating a slight decline in TEQs of PCDD/Fs with increasing distance from the MSWI stack. The ordinary kriging interpolation technique was selected to create a contour map, which intuitively showed that a limited surrounding area (≤1,000 m from the stack) was obviously influenced by the MSWI.     

Abstracts to forthcoming papers

Food is the major source of metal exposure for the nonsmoking general population. Food samples of plant and animal origin from Ismailia, Egypt, were analyzed for the content of cadmium (Cd), lead (Pb), chromium (Cr), zinc (Zn), and copper (Cu) using AAS. The Cr, Zn, and Cu concentrations were in the range of 1.7–249?µg?kg^?1 wet weight (ww), 2–66?mg?kg^?1?ww, and 0.5–3.46?mg?kg^?1?ww, respectively. The mean daily intake of Cr, Zn, and Cu was 28.9?µg day^?1, 8.55?mg day^?1, and 1.7?mg day^?1, respectively. The intake estimates are within the range of the recommended intake established internationally. Concentrations of Cd and Pb were in the range of 10–321?µg?kg^?1?ww and 31–1200?µg?kg^?1?ww, respectively. The weekly dietary intake for Cd and Pb (4.02 and 20.4?µg?kg^?1 b.w, respectively) is lower than the FAO/WHO PTWI. Bread is the foodstuff that provided the highest rate of Pb and Cd (62 and 46% of the daily intake) to adults in Ismailia city.     

Combined effects of 2,3,7,8-tetrachlorodibenzo- p -dioxin and polychlorinated biphenyl congeners in rats

The objective of this work was to evaluate potential interactions between 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD) and polychlorinated biphenyls congeners (PCBs) in rats. Groups of five adult female rats were given 0, 2.5, 25, 250, or 1000?ng TCDD/kg body weight/day or TCDD in combination with a mixture of PCB congeners at a concentration of 2 or 20?µg?kg^?1 body weight/day by gavage for 28 days. After the 28-day treatment period, the rats were killed for the analysis of biochemical, liver enzyme activities, and hematological and pathological end points. Growth suppression, increased absolute and relative liver weights, and decreased thymic weight were observed in the 1000?ng TCDD group alone, or the groups receiving a mixture of 1000?ng TCDD and 2 and 20?µg PCBs. TCDD-increased liver and thymic weights were not altered by PCBs; however, growth suppression was more pronounced in animals receiving 1000?ng TCDD and 2?µg PCBs. Increased hepatic microsomal methoxy resorufin-O-demethylase and ethoxy resorufin-O-deethylase activities occurred in 250 and 1000?ng?kg^?1 TCDD-treated animals, which were antagonized by PCBs. Effects of 250?ng TCDD on serum cholesterol and liver uridine diphosphate glucuronosyl transferase activity were reduced by 20?µg PCBs. Treatment with 1000?ng TCDD increased serum albumin, decreased liver vitamin A, increased kidney vitamin A, and liver microsomal glutathione-S-transferase activity, which were not affected by PCBs. Decreased hemoglobin, platelet, packet cell volume, and red cell indices were observed in TCDD-treated rats, but no interactive effects were seen. Histopathological evaluation revealed that liver, thyroid, and thymus were the target organs, but the effects of co-exposure to PCBs and TCDD were variable. These results indicate that the mixture effects of PCBs and TCDD may be additive, synergistic, or antagonistic depending on the dose level and end points measured.     

Polychlorinated biphenyl (PCB) residues in European roe deer (Capreolus capreolus) and red deer (Cervus elaphus) from north-western Poland

The purpose of this study was to evaluate polychlorinated biphenyls (PCBs) contamination levels in roe and red deer from north-western Poland and to assess environmental pollution in this area. A quantitative analysis was conducted using a capillary gas chromatography/mass spectrometry method. The mean concentrations of ΣPCBs (sum of PCBs: 28, 52, 101, 138, 153, 180) in liver samples were 30.24±12.35 ng·g^?1 of lipid weight (l.w.) in roe deer and 60.13±14.23 ng·g^?1 l.w. in red deer, compared with 24.21±10.02 and 45.22±9.77 ng·g^?1 in the lungs of roe and red deer, respectively. PCBs 138, 153 and 180 were the dominant congeners in the liver samples of the analysed animals, whereas PCB 138 and 153 in the lungs. TEQs levels calculated for only dioxin-like PCBs were low: 0.32 and 0.29 pg WHO-PCB-TEQ·g^?1 fat in liver of red deer and roe deer, respectively. The mean PCB concentrations obtained in our study for organs of roe deer and red deer were several times lower than those reported elsewhere. These findings show that the investigated roe and red deer originated from an area with low levels of PCB contamination.     

Pollution characteristics and potential health risk of polychlorinated dibenzo-p-dioxins and dibenzofurans (PCDD/Fs) in soil/sediment from Baiyin City, North West, China

In order to better understand the environmental behaviors of persistent organic pollutants, the characteristics of polychlorinated dibenzo-p-dioxins and dibenzofurans (PCDD/Fs) were investigated in twenty-three soil/sediment samples from Baiying City, Northwest China, in 2008. The possible sources and potential health risk of PCDD/Fs were also discussed. The concentrations of PCDD/Fs in nineteen soil samples varied between 20.13 and 496.26 pg/g dry weight (dw.), with an average value of 125.59 pg/g dw. The highest International Toxic Equivalent (I-TEQ) of PCDD/Fs (8.34 pg/g dw.) in soil was found at sample S1 collected from proximity to a copper metallurgy plant. The concentrations of PCDD/Fs in four sediment samples ranged from 37.69 to 491.49 pg/g dw., with an average value of 169.95 pg/g dw. The highest I-TEQ of PCDD/Fs (8.56 pg/g dw.) in sediment was found at sample S12 collected from the East big ditch with waste water discharged into the Yellow River. The results indicated that PCDD/Fs contamination of soil/sediment is originated from three sources: chlorine-containing chemicals, non-ferrous metal industrial PCDD/Fs emission and coal burning. The health risk exposure to PCDD/Fs through soil, dust ingestion and dermal absorption ranged from 0.0006 to 0.0134 pg/kg/day Word Health Organization’s toxic equivalent in 1998 (WHO₁₉₉₈-TEQ) with mean values 0.0032 pg WHO₁₉₉₈-TEQ for adults and varied between 0.0012 and 0.0256 pg/kg/day WHO₁₉₉₈-TEQ with mean values 0.006 pg/kg/day WHO₁₉₉₈-TEQ for children, respectively. These results indicated that health risk of PCDD/Fs for children should be paid more attention.     

Residues of PCDD,PCDF, and PCBs in some marine organisms in Lake Temsah,Ismailia, Egypt

Residues of PCDDs/F, non-ortho, mono-ortho PCBs, and other PCBs were monitored in the tissues of mullet fish, bolti fish, bivalves and crab taken from Lake Temsah, at Ismailia, Egypt.

Results showed that 2,3,7,8 Tetra CDD and 1,2,3,7,8 Penta CDD were the most frequently detected PCDD congeners. Similarly, 2,3,7,8 Tetra CDF, 1,2,3,7,8 Penta CDF and 2,3,4,7,8 Penta CDF were the most frequently detected PCDF congeners. No relationship was apparent between the concentrations of detected PCDDs congeners and the degree of chlorination, except with crab samples in which an increase in the chlorination coincided with a decrease in the concentrations of the congeners.

In PCDF congeners, detected residues have had a reversed relationship with chlorination increase. In PCDD congeners, Octa CDD had the highest detected concentrations in the two fish species, while in the bivalves and crab, 2,3,7,8 Tetra CDD had the highest concentrations. The mullet fish had the highest total PCDDs concentration, at 0.398?pg/g fresh weight, followed by crab at 0.395?pg/g fresh weight, then bivalves and bolti fish at 0.187 and 0.062?pg/g fresh weight, respectively. In all the examined organisms, the total concentrations of PCDFs were much higher than the total concentrations of the PCDD congeners. The WHO–TEQ values were 11.92, 39.12, 25, and 3.6?pg/g fresh weight, for mullet fish, bolti fish, bivlaves and crab, respectively. The concentration of the mono-ortho congeners CB 118 was the highest detected of all non-ortho and mono-ortho PCBs congeners, with values of 0.382, 0.022, 0.231 and 0.357?ng/g fresh weight, in mullet fish, bolti fish, bivalves and crab, respectively. The WHO–TEQ concentrations were 0.799, 0.003?pg/g fw, 0.05?pg/g fresh weight, 0.676?pg/g, and 0.799?pg/g fresh weight, for the same species, respectively. The total concentration of PCBs 28, 52, 95, 99, 101, 105, 110, 118, 138, 146, 149, 151, 153, 170, 177, 180, 187 were 6.86?ng/g fresh weight for mullet fish, 0.2?ng/g fresh weight, for bolti fish, 2.72?ng/g fresh weight for bivalves and 2.8?ng/g fresh weight for crab, respectively.     

Lead and copper in the sclerotium of the mushroom Pleurotus tuber-regium (Osu): assessment of contribution to dietary intake in southeastern Nigeria

The concentrations of lead and copper in sclerotium of the mushroom Pleurotus tuber-regium widely consumed in Southeastern Nigeria were determined. The specimens purchased from different markets were mineralized with H₂SO₄ and H₂O₂ and analyzed using flame atomic absorption spectrophotometer. The concentrations of Pb ranged from 0.2?±?0.1?mg?kg^?1 to 0.8?±?0.5?mg?kg^?1 with approximately 91% of the results being below 1?mg?kg^?1. The concentrations of Cu ranged from 0.5?±?0.2?mg?kg^?1 to 1.2?±?0.6?mg?kg^?1 with 78% of the results below 1?mg?kg^?1. The results were compared with the literature and levels set by regulatory authorities, with the conclusion that the consumption of sclerotium does not pose a toxicological risk. The low Pb content of the studied products would contribute to only about 1% of the provisional tolerable weekly intake of Pb. The Cu contents would contribute to nutritional intake of the metal in the general population. It is recommended that the outer layers of the sclerotia be properly scrapped before use to reduce metal contamination from exogenous sources.     

喜马拉雅山区葇籽草和棘豆样品中PCBs、PBDEs和PCDD/Fs的分析

应用同位素稀释-高分辨气相色谱/高分辨质谱(HRGC/HRMS)法分析了喜马拉雅山区海拔5000 m以上的葇籽草和棘豆样品中多氯联苯(PCBs)、多溴联苯醚(PBDEs)和二噁英(PCDD/Fs)的含量.这两种植物样品中污染物含量与世界其它偏远地区的水平基本保持一致.其中PCBs的总含量在1.94—3.62 ng.g-1干重(dw)范围内,平均值为2.60 ng.g-1dw;PCB-28和PCB-52的浓度明显较高,约占7种指示性PCBs总量的90%以上.14种PBDEs的总浓度在83.3—142 pg.g-1dw之间,平均值为116 pg.g-1dw;除BDE-85、-138、-154,以及高溴代的BDE-190和BDE-209未检出外,其它9种单体均有不同程度的检出,且以低溴代的BDE-28为主,含量占45%以上.样品中PCDD/Fs基本上未检出.由于样品采集点位于喜马拉雅山人迹罕至的珠穆朗玛峰北坡地区,周围并无工业污染源,因此植物样品中PCBs及PBDEs可能是污染物发生大气长距离传输和生物富集的结果.     

Effects of deltamethrin on serum calcium and corpuscles of Stannius of freshwater catfish,Heteropneustes fossilis

Adult male deer mice were exposed every other day for a period of 11 days to either 7,12-dimethylbenzanthracene (DMBA; CAS# 57-97-6) or benzo[b]fluoranthene (BbF; CAS# 205-99-2) (0, 0.3, 1, 3, 10, or 30?mg?kg^?1). Immune endpoints assessed were lymphocyte proliferation, macrophage pinocytosis, and the antibody plaque-forming cell (PFC) response. Cytochrome P450 (CYP450) activity was assessed using ethoxyresorufin-O-deethylase (EROD) and pentoxyresorufin-O-deethylase (PROD). Macrophage pinocytosis was not altered by either compound. Both T- and B-cell proliferations were significantly increased by DMBA at 0.3 or 1?mg?kg^?1 and by BbF at 10 or 30?mg?kg^?1, but decreased by DMBA at 30?mg?kg^?1. Sheep red blood cell (SRBC)-specific-IgM production, as measured by the PFC response, was the most striking adverse immune effect observed and was significantly suppressed compared to control at all treatment concentrations for both compounds. EROD activity was markedly induced by DMBA at 30?mg?kg^?1, while BbF produced induction at 1, 10, or 30?mg?kg^?1. No marked effect on PROD activity was noted following DMBA treatment, but BbF-induced PROD activity at 1, 10, or 30?mg?kg^?1. Unexpectedly, four of six mice in the 30?mg DMBA?kg^?1 group did not survive to the end of the experiment, and one animal died in both the 3 and 10?mg?kg^?1 treatments. The calculated LD₅₀ was 20.8?mg DMBA?kg^?1. The PFC response in deer mice was a more sensitive endpoint than CYP450 activity, suggesting that utilization of CYP450 endpoints in risk assessment without assessment of immune function, specifically antibody production, might possibly underestimate the risk to wild rodents environmentally exposed to polycyclic aromatic hydrocarbons.     

Polychlorinated-dibenzo-p-dioxins, -dibenzofurans and -dioxin-like polychlorinated biphenyls in aquatic organisms from lake Kasumigaura,Japan

Polychlorinated-dibenzo-p-dioxins (PCDDs), -dibenzofurans (PCDFs) and -dioxin-like polychlorinated biphenyls (DLPCBs) were determined in aquatic wildlife of Kasumigaura Lake (KUL), Japan from 1978 to 2001. Two plankton species elucidated several fold greater concentrations (2400–7800) than small tiger fish (310–6500), shrimp (160–1100), and three large fish namely, black bass (120–240), carp (94–120) and mullet (54) on pg/g fat. PCDD homologues were predominant accumulants with >68–<95% contribution and remaining was shared by PCDFs. Accumulation, non-ortho DLPCBs in plankton (3500–9200), shrimp (1600–8600) and small fish (2000–8800) and large fish (1300–3900) on ng/g fat basis were several orders magnitude greater than PCDD/DFs. The mono-ortho DLPCBs in large fish species were 23?000–83?000?ng/g fat and which it is accounted 94.3–95.9% the total dioxin-like PCBs accumulation. Temporal trends of PCDDs, PCDFs, non-ortho PCBs and TEQ in shrimp and small tiger fish were varied. The mullet had minimum toxic equivalency “TEQ” (14?pg?TEQ/g) followed by plankton Neomysis intermedia (25?pg?TEQ/g), small tiger fish (mean: 33, ranges 14–66?pg?TEQ/g), plankton Cyclopus vicinus (34?pg?TEQ/g), carp (mean: 35, ranges 32–38?pg?TEQ/g), shrimp (mean: 38, ranges 11–68?pg?TEQ/g) and black bass (mean: 59, ranges 38–79?pg?TEQ/g) on fat basis. In all the samples, PCDD was predominant TEQ contributor followed by PCDFs and DLPCBs. The contribution of mono-ortho DLPCBs to the total TEQ was 0.52–0.92 in large fish.     

Monitoring and risk assessment of polychlorinated biphenyls (PCBs) in agricultural soil from two industrialized areas

For monitoring and risk assessment, levels and distributions of Σ₂₉ PCBs in paddy soil samples collected from Gwangyang (10 sites) and Ulsan (20 sites), heavily industrialized cities in Korea, were investigated using high-resolution gas chromatography/high-resolution mass spectrometry. Overall, total concentrations of Σ₂₉ PCBs in Gwangyang (216.4–978.6 pg g^?1 dw) and Ulsan (273.8–1824.1 pg g^?1 dw) were higher than those (106.6–222.6 pg g^?1 dw) in agricultural soil from Anseong in Korea. The TEQ (toxic equivalency) values from Gwangyang (0.06–0.40 ng TEQ kg^?1 dw) and Ulsan (0.06–0.22 ng TEQ kg^?1 dw) were higher than those (0.04–0.11 ng TEQ kg^?1 dw) in Anseong but lower than the WHO threshold level (20 ng TEQ kg^?1). However, one of the most toxic congeners, PCB 126, gave the highest concentration, possibly posing a risk to the biota. Seven indicator PCB congeners contributed to 50–80% of the total concentration of Σ₂₉ PCBs, indicating the 7 PCBs can be used as valuable indicators for monitoring. The principal component analysis and cluster analysis for the homologue profiles of PCBs indicated that all the samples from both cities had the similar PCB contamination patterns, and the major sources of the PCB contamination were most likely from the usage of Aroclor 1254 than those of Aroclors 1242 and 1260. These PCB technical mixtures were possibly significantly used by various industries including iron and steel industries in Gwangyang and petrochemical and shipbuilding industries in Ulsan.     

电子垃圾拆解对台州氯代/溴代二噁英浓度和组成的影响

电子垃圾拆解会导致有毒有害污染物向大气的排放,造成环境污染的产生。为了解电子垃圾拆解及废旧金属再生活动对拆解地及邻近地区空气质量的影响,对台州峰江金属再生园区附近及对照区路桥市区大气中(气态和颗粒态)氯代二噁英(PCDD/Fs)、溴代二噁英(PBDD/Fs)的含量、同系物组成及气/固分配规律进行了研究,通过相关性分析探讨了PCDD/Fs和PBDD/Fs的可能来源。结果显示,金属再生园区冬季采样期间17种2,3,7,8-PCDD/Fs和8种2,3,7,8-PBDD/Fs的平均浓度分别为212.2 pg·m-3和17.6 pg·m-3,夏季采样期间的平均浓度分别为84.5 pg·m-3和5.4 pg·m-3,均显著高于对照点。夏季采样期间对照点处于再生园区的下风向,其二噁英浓度高于冬季,说明其受到了金属再生园区的明显影响。基于相关性分析的结果,塑料焚烧是金属再生活动中氯代和溴代二噁英的主要来源。初步的暴露风险评价表明,金属再生园区附近居民每日摄入的二噁英含量远远超过世界卫生组织规定的人体每日耐受量(1~4 pg W-TEQ·kg-1·d-1)。上述研究结果为规范电子垃圾拆解活动提供了基础数据。