Bioaccumulation of organochlorine contaminants in fish species from Lake Qarun,a protected area of Egypt

The purpose of this study was to determine concentrations of organochlorine pesticides (OCPs) and polychlorinated biphenyls (PCBs) in Nile tilapia (Oreochromis niloticus) and Bouri fish (Mugil cephalus) from Lake Qarun, a protected area of Egypt, and evaluate the relative ecological risk of these compounds. Different tissues of the fish species were analyzed for 26 chlorinated pesticides and 29 PCB congeners. Total concentrations (µg/kg wet weight, ww) of OCPs ranged between 1487 and 6217 (mean: 3260) and of PCBs between 9.0 and 61 (mean: 34). The trend of detected organochlorine pollutants was: endrin aldehyde > dieldrin > hexachlorobenzene > PCBs > endrin > 1,1,1-trichloro-2,2-bis(p-chlorophenyl)ethanes (DDTs). Heptachlor epoxide; oxy-, cis-, and trans-chlordane; trans-nonachlor; β-hexachlorocyclohexane; δ-hexachlorocyclohexane; and endosulfan I and endosulfan sulfate levels were below the detection limit. The ratios of (1,1-dichloro-2,2-bis(p-chlorophenyl)ethylenes [DDEs] + 1,1-dichloro-2,2-bis(p-chlorophenyl)ethanes [DDDs])/ΣDDTs in fish tissues indicated no recent DDT exposure. Concentrations of DDTs and PCBs were generally comparable or higher than those found in studies of similar species worldwide. The concentrations of hexachlorobenzene, dieldrin, and endrin aldehyde in fish muscles exceeded the maximum residue level recommended by various organizations.     

Polychlorinated biphenyls and organochlorine pesticides in amniotic fluids of pregnant women in south-central Turkey†

The concentrations of organochlorine pesticides (OCPs) and polychlorinated biphenyls (PCBs) were determined in amniotic fluid of 200 pregnant women from the Cukurova region of Turkey. The concentrations of OCPs [hexachlorocyclohexane (HCH), hexachlorobenzene (HCB), dichlorodiphenyl trichloroethane (p,p′-DDT), and various metabolites], and different PCB congeners (28, 52, 101, 118, 138, 153, 180) were determined by gas chromatography with electron capture detection as follows: HCB 6.6 ± 4.7, ΣHCH 21.6 ± 14.2, ΣDDT 12.5 ± 7.5, and ΣPCBs 74.0 ± 54 ng mL^?1. Correlations of maternal or gestational age and levels of OCPs and PCBs were not significant. The levels of these organochlorine compounds (OCs) were below detection limit for 5% of the samples, 80% contained more than one OC. This study illustrates that prenatal exposure of a fetus to OCs is prevalent in the Cukurova region.     

Biomonitoring of polychlorinated byphenyls contamination in the supralittoral environment using the sandhopper Talitrus saltator (Montagu)

We evaluated the use of Talitrus saltator as biomonitor of polychlorinated byphenyls (PCBs) contamination of the supralittoral zone of Mediterranean sandy shores, an area not yet investigated about the presence of these pollutants. Twenty of 22 PCB congeners analysed were detected and quantified in sand and sandhoppers' samples collected in 6 different sites along the Tyrrhenian coast of Central Italy. Among the congeners analysed, PCB 153 and PCB 138 were the most abundant both in amphipods and sand samples and, regarding the congener pattern analysis, hexa-, hepta- and penta-PCBs were the most abundant congeners in sandhoppers. Though hydrophobic compounds, such as PCBs, bind strongly to sand and sediments, PCB concentrations were higher in T. saltator than in the sand revealing a good ability of this species to accumulate this class of contaminants. The concentration of each PCB congener recorded in tissues of sandhoppers showed significant differences among sampling sites revealing a good ability of these species to accumulate PCBs at different concentrations depending on the contamination levels of the sampling site. Therefore, our results suggest the possible utilisation of T. saltator as a biomonitor of PCB contamination of the supralittoral zone of Mediterranean sandy shores.     

Persistent organochlorine contaminants in human tissues of the Czech and Slovak populations

The persistence of lipophilic organochlorine substances leads to their incorporation into the food chain and subsequent uptake by humans. Due to their use in the past, Czech and Slovak countries belong to the countries with a relatively high body burden of organochlorines. Levels of PCBs in human tissues based on the congener‐specific analysis are reported in this paper. Samples were analysed for the most abundant PCB congeners. Prevalent persistent organochlorine pesticides and their isomers/metabolites have also been included. The present study is focused on following areas: i) distribution of analysed substances in the various human tissue samples from selected regions of the Czech and Slovak Republic and ii) comparison with the results from other foreign and local studies.     

Congener-specific analysis of polychlorinated biphenyl in human blood from Japanese

Polychlorinated biphenyl (PCB) congeners were analyzed by high resolution gas chromatography/high resolution mass spectrometry (HRGC/HRMS) of whole blood samples taken from 24 healthy adult Japanese volunteers (12 males and 12 females; age range 25–46 years). On average, 95 PCB congeners were detected in whole blood samples. The mean of total PCB concentration in whole blood was 771.9 pg g^–1 whole blood (139.6 ng per g-lipid). Congener-specific analysis identified the predominant PCB congeners as #153 (22.2), #180 (11.6), #138 (8.4), #182/187 (6.6), #118 (5.6), #163/164 (5.0), #99 (3.9), #74 (3.6), #146 (3.3), #170 (3.0) and #156 (2.2), representing 75.6 of all PCBs detected in the human blood samples. Among the predominant PCB congeners, #153, #180, #138, #187 #118, #99 and #74 had chlorine as the substituent at the 2-, 4- and 5- positions of the phenyl-ring. In human blood in Japanese individuals, it is assumed that these congeners would be characteristic of the entire population, based on the relation between PCB ingestion and metabolism. Measuring 209 PCB congeners has the advantage of providing detailed information regarding the congener distribution within the blood samples, which can be compared to congener patterns in other matrices. Congener-specific analysis of 209 PCB congeners is especially useful in evaluating human exposure to PCBs.     

Accumulation, distribution and transformation of DDT and PCBs by Phragmites australis and Oryza sativa L.: II. Enzyme study

Two wetland plant species, Phragmites australis and Oryza sativa, were grown in a glasshouse under hydroponics conditions. Enzyme extracts from different parts of the plants were used to determine the transformation rate of o,p′-DDT, p,p′-DDT and PCBs. The organic pollutants were directly spiked into the enzyme extracts, and samples were collected every 30 min and analyzed with a GC-ECD. Root extracts of P. australis readily degraded and transformed DDT and some PCB congeners with a low degree of chlorination. In contrast, crude extracts of O. sativa showed no appreciable degradation or transformation of DDT or PCBs. Inhibition studies indicated that the degradation and transformation of both DDT and PCBs by P. australis enzymes were partly mediated by peroxidase and the plant P-450 system. PCBs with a high degree of chlorination were highly resistant to transformation or degradation by plant enzymes. Both wetland plant species accumulated substantial quantities of the persistent organic chemicals but had different degradation capacities. The enzyme systems in P. australis were much more effective that those in rice in the degradation and transformation of the organic pollutants.     

Levels and congener distributions of PCDDs,PCDFs and dioxin-like PCBs in environmental and human samples: a review

The term “dioxins” is often used in a confusing way. In toxicological considerations—and also in the present report—the term is used to designate the PCDDs, the PCDFs and the coplanar (“dioxin-like”) PCBs, since these classes of compounds show the same type of toxicity. Because of the large number of congeners, relevant individual congeners are assigned with a toxic equivalency factor (TEF) that relate their toxicity to that of tetrachlorodibenzo-p-dioxin (TCDD) (2,3,7,8-TCDD) and are to be evaluated as dioxins. Each concentration of an individual congener in a mixture is multiplied with its TEF, and the resulting TCDD equivalents are added up and expressed as WHO-endorsed toxic equivalents (WHO-TEQ). Polychlorinated dibenzo-p-dioxins (PCDDs) and polychlorinated dibenzofurans (PCDFs) are mainly the by-products of industrial processes (such as metallurgical processing, bleaching of paper pulp, and the manufacturing of some herbicides and pesticides) but they can also result from natural processes like volcanic eruptions and forest fires. Waste incineration, particularly if combustion is incomplete, is among the largest contributors to the release of PCDDs and PCDFs into the environment. Due to their persistence, PCDDs, PCDFs and PCBs are part of the so-called persistent organic pollutants group of compounds that also include some chlorinated pesticides. Since they have a high lipophilicity and resist transformation, they bio-accumulate in animal and human adipose tissues. Consumption of food is considered as the major source of non-occupational human exposure to PCDD/Fs with foodstuffs from animal origin accounting for more than 90% of the human body burden. With meat, dairy, and fish products being the main contributors. The aim of the present review was to summarize experimental data regarding dioxin emissions from contaminated and uncontaminated biological and environmental samples, from the available literature. The information will be presented chronologically with respect to distribution in human milk, serum; food, water, air, soils and sediments.     

Analysis of PCB levels in snow from the Aconcagua Mountain (Southern Andes) using the stir bar sorptive extraction

This paper presents a first result of an investigation of the presence of anthropogenic pollutants named polychlorinated biphenyls (PCBs, sum of 25 congeners) in snow samples in the Aconcagua Mountains in the Andean Range, along an altitudinal gradient. Samples were taken during an expedition in 2003 and analysed by using a specific technique of thermodesorption and GC-MS adapted to small amount of sample. Mountain ecosystems could be efficient natural trap of persistent organic pollutants (POPs) transported by the atmosphere, and it is shown in this note that PCBs are also present in snow samples but at low concentrations, levels ranged from 0.02 to 0.190 ng/L. The detected congeners were those more persistent (PCB 138, PCB180) and compared to other mountain and cold areas around the world, detected levels are in the low range indicating that pollution levels are lower in the southern hemisphere. This results points out the need of investigating with some more detail the role of mountains in the trapping of POPs and the associated risks including the climate change.     

Seasonal and spatial character of PCBs in a chemical industrial zone of Shanghai,China

As one of China’s great metropolises, Shanghai is suffering from the impact of manufacture and the use of chemical industrial products, and it faces serious pollution from polychlorinated biphenyls (PCBs). Therefore, in this study, in order to assess the seasonal and spatial character of contamination from chemical industrial zones, the concentrations of PCBs have been measured in various environmental media, including soil, leaves, and atmospheric particulate samples collected in a chemical industrial zone of Shanghai and compared with samples from presumably unpolluted sites of rural areas. In soils, the PCB concentrations ranged from 0.5 ng g⁻¹ (unpolluted site) to 586.85 ng g⁻¹ (chlor-alkali industry site). The concentrations of PCBs in evergreen leaves ranged from 0.3 ng g⁻¹ to 32.46 ng g⁻¹, and more chlorinated biphenyls congeners, such as penta-biphenyls and hexa-biphenyls, were the dominant contributors in winter and spring. Seasonal differences and the constitution patterns of congeners might be affected by the temperature and industrial activities. The PCB concentrations in the leaves of deciduous trees increase over time as the leaves grow. The PCB concentration in atmospheric particulates was in the range of 9.22–14.15 × 10³ pg m⁻³, which might be the result of influence from climate and industrial activities. The relativity of PCB contents among the environmental media was discussed. The results in this paper provide an important profile of the current contamination status of a key chemical industrial zone in China.     

Chorioallantoic membrane as a non-lethal sampling method for polychlorinated biphenyls analysis in the northern diamondback terrapin (Malaclemys terrapin terrapin)

Polychlorinated biphenyls (PCBs) are documented endocrine-disrupting chemicals. This study examined the bioaccumulation of PCBs and the utility of the chorioallantoic membrane (CAM) as a non-lethal sampling technique for PCB analysis in the northern diamondback terrapin (Malaclemys terrapin terrapin), a species endemic to US East Coast salt marshes. To determine the viability of the CAM as a surrogate for PCB burdens within this species, maternal transfer of PCBs to CAM and egg samples was studied. Egg and CAM samples were collected from populations in Cape May County, NJ and Jamaica Bay, NY; liver samples were collected only from NJ terrapins. PCB congeners were detected in all sample types, but less-chlorinated congeners preferentially partitioned in the CAM. Liver and egg sample PCB concentrations were strongly correlated (p=0.002, r _s=0.883), but PCB concentrations of CAM were not strongly correlated to liver (p=0.035, r _s=0.733) and egg samples (p=0.036, r _s=0.484). Examination of homologue groups indicated a strong correlation between penta- and hexachlorinated biphenyls for all sample types. This study shows that maternal transfer of PCB contaminants occurs with selective partitioning of congeners into the CAM, and that analysis of the CAM alone may not reflect total PCB body burdens in this species.     

Clam‐sediment accumulation factors for polychlorinated biphenyl congeners at a contaminated estuarine marsh

Clam‐sediment accumulation factors for hexa‐, hepta‐ and octa‐chlorobiphenyls were estimated at an intertidal marsh that has been contaminated with Aroclor 1268. Accumulation factors for PCB congeners with K _ow > 6.5 were in the range of 0.07–0.88, indicating that their uptake was hindered by steric factors, contamination levels, non‐equilibrium conditions and stronger affinity to sediment organic carbon. Biota‐sediment accumulation factors (BSAFs) were negatively correlated with log K _ow of superhydrophobic PCB congeners. BSAFs estimated based on 2,3,7,8‐TCDD equivalents of PCBs were 2‐fold greater than those derived from total PCB concentrations.     

Detection of polychlorinated biphenyls employing chemical dechlorination followed by biphenyl whole cell sensing system

Polychlorinated biphenyls (PCBs) are a mixture of 209 individual chlorinated compounds commonly known as PCB congeners. These compounds are hydrophobic and are persistent in the environment. Their use was banned in the US a few decades ago because of harmful health effects. Therefore, detection of PCBs in environmental samples is increasingly important. To that end, we have developed a two-step simple and sensitive method for the detection of total PCBs. Specifically, our method involves dechlorination of PCBs to biphenyl followed by detection of biphenyl using a whole cell sensing system as the detection system. The whole cell sensing system consists of cells of the strain Pseudomonas pseudoalcaligenes KF707 harboring plasmid pSD7000. Plasmid pSD7000 contains the gene of lacZ, a reporter protein under the control of the bph operon. The detection is achieved through the emission of light afforded by the expression of reporter protein triggered by the presence of biphenyl. Due to the fact that this operon is activated only by few PCB congeners, a chemical dechlorination method was employed to convert all PCBs to biphenyl, and thus all the PCBs present in a given sample are able to be detected. The results showed that PCB congeners were rapidly (30?min) and efficiently (>98.5%) dechlorinated to biphenyl using a Mg/K₂PdCl₆ catalyst, and the biphenyl could be subsequently quantified using the whole cell sensing system. This hybrid analytical method that combines classical dechlorination with novel biosensing methods may find applications in the on-site monitoring of PCBs contamination levels.     

Accumulation of persistent organic pollutants in the food chain of lake baikal

Lake Baikal is the deepest and oldest freshwater lake in the world containing about 20% of the world's fresh water. The present state of its contamination with organic pollutants was studied during 1997–1998 by collecting samples of sediments, phytoplankton, Zooplankton, sponges, aquatic plants, algae, muscles of various fish species, eggs of various birds and blubber of seals. Samples were prepared and analysed using GC‐MS for semivolatile priority pollutants on the US EPA list, for the presence of organochlorine pesticides and for PCBs. The results showed that there was pronounced bioaccumulation of persistent organochlorine compounds along the trophic chain, leading to substantial residues of organochlorine compounds in seals (e.g. 0.87–25.3 ppm of p,p'‐DDT in blubber).     

Detailed analysis of PCBs and PCDD/Fs impurities in a dielectric oil sample （ASKAREL Nr 1740） from an imported transformer in China

Homolog and congener profiles of polychlori- nated biphenyls （PCBs）, polychlorinated dibenzo-p- dioxins （PCDDs） and polychlorinated dibenzofurans （PCDFs） in commercial PCBs formulations are useful information for the source appointment of PCBs contam- ination as well as the risk assessment caused by potential exposure. Dielectric oil （ASKAREL Nr 1740） in an imported transformer found in China was sampled and analyzed by isotope dilution technology using high resolution gas chromatography-high resolution mass spectrometry （HRGC/HRMS）. The detailed homolog and congener profiles of PCBs obtained were compared with those of known Aroclor formulations. High similarity in the homolog profile between the oil sample and Aroclor 1260was found, with the hexachlorinated and hepta- chlorinated biphenyls accounting for more than 80.2% of the total PCBs concentration. Severn indicator PCBs contribute about 30%, while 12 PCB congeners （i.e., # 153, #143, #168, #180, #149, #165, #138, #170, #190, #187, #174, #181） account for more than 50% of the total PCB concentrations. Total concentration ofPCDDs, PCDFs and dioxin-like PCBs （DL-PCBs） was found to be 740 ng TEQ/g, of which 620 ng TEQ/g came from DL-PCBs. The contribution of PCDDs to the total TEQ was neglectable. The concentration of PCDFs homologs follows the order of OCDF 〉 HxCDFs 〉 HpCDFs 〉 PeCDFs 〉 TeCDFs, which is in consistence with the previous study on Aroclor 1260. Three DL-PCBs congeners （i.e., #118, #156, #157） accounted for 77% of the total concentration of DL-PCBs, also they contribute 72% in the TEQ caused by DL-PCBs.     

Post-war levels of persistent organic pollutants (POPs) in air from Serbia determined by active and passive sampling methods

For the duration of the war accident in former Yugoslavia, several industrial and military targets were burnt and damaged, resulting in a significant release of persistent organic pollutants. Locations heavily targeted in the attacks were later defined by UNEP as four “hot spots”: Kragujevac, Novi Sad, Pancevo and Bor. We analyzed concentration levels of pollutants collected in 2004 and 2005 in air samples from the city of Kragujevac, Serbia, following the war accident of 1999. Pollutants included polycyclic aromatic hydrocarbons (PAHs), hexachlorocyclohexane (HCH), dichloro-diphenyl-trichloroethane (DDT), dichloro-diphenyl-dichloroethylene (DDE), dichloro-diphenyl-dichloroethane (DDD) and polychlorinated biphenyls (PCBs). We present results obtained during air sampling campaign conducted in July 2004 by the active sampling method; and during September 2004–June 2005 by the passive sampling method. Our findings show the occurrence of residual quantities of DDT, HCH, PCBs and PAHs in air samples. High levels of PCBs are probably due to the destruction of transformers during the war accident.     

Polychlorinated biphenyls and their hydroxylated metabolites in the serum of e-waste dismantling workers from eastern China

A number of studies have reported on the exposure of e-waste dismantling workers to significantly high concentrations of halogenated organic pollutants such as polychlorinated biphenyls (PCBs) and polybrominated diphenyl ethers. Such exposure can have adverse health effects. However, little information on the metabolites of these contaminants exists. In this study, we investigated PCBs levels and their hydroxylated metabolites (OH-PCB) in the serum of e-waste workers in Taizhou in eastern China. Our results indicate elevated PCB and OH-PCB levels in the serum of the workers, with medians of 443.7 and 133.9 ng/g lw, respectively. Tri- to hexachlorinated PCB congeners were the dominant homologue groups in all of the samples. 4-OH-CB107 was the predominant homologue among the hydroxylated metabolites, accounting for 88.9% of the total OH-PCB concentrations. While dietary sources (e.g., fish) appear to be an important route for PCB accumulation in non-occupational exposure groups, exposure via ingestion of house dust and inhalation of pollutants derived from the recycling of PCB-containing e-wastes may primarily contribute to the high body burden observed in the occupational groups. Since we found concentrations of metabolites higher than those of their parent compounds, further studies need to pay more attention to their bioaccumulation and toxicity.     

Spatial and seasonal variation of polychlorinated biphenyls in Songhua River, China

The spatial and seasonal variation of polychlorinated biphenyls (PCBs) were investigated in water and sediment samples collected from Songhua River, China, from 2007 to 2008. The total concentration of PCB congeners ranged from 1.1 to 14 ng/l in water and 0.26–9.7 ng/g dry weight (dw) in sediment. The results of seasonal variation may suggest an impact to PCB concentration in water from its atmospheric input, the dilution to PCBs concentrations of high stream in summer, and a general trend towards increased volatilization in warmer conditions. From PCBs concentrations comparison between upstream and downstream of industrial urban cities, it was obvious that industrial urban cities reflect an important pollutant source for PCBs in our study, also with the evidences of high concentrations of PCBs occurring in high development industry and residential areas. Meanwhile, the homologue profile of PCBs in Songhua was analyzed, whose comparison with published data indicates that the sources of PCBs accumulated in the sediment may also came from the residue of PCBs production in China. Total five dioxin-like PCBs (CB-77, 81, 105, 114, and 126) and nine (CB-77, 81, 105, 114, 118, 123, 126, 156, and 167) were found in Songhua water and sediment.     

中国东海抹香鲸体内多氯联苯的组成特征及毒性当量

用气相色谱-质谱联用仪测定了一只中国东海海域抹香鲸(Physeter macrocephalus)皮脂24种多氯联苯(PCBs)同系物的含量,并分析了其组成特征以及国际毒性当量.结果表明,东海海域抹香鲸皮脂PCBs的湿重含量为1.12μg.g-1;PCBs同族体中以含6和5个氯原子的化合物为主,高氯代PCBs占总量的92.10%;PCBs同系物中以PCB153、PCB138、PCB101和PCB149居多,分别占到PCBs总量的21.28%、15.97%、10.29%和10.23%;抹香鲸皮脂的TEQs含量为1663.07 pg.g-1,其毒性主要来自PCB126,其次是PCB123和PCB118;初步推断中国东海海域的抹香鲸受PCBs污染程度较轻.     

Characterization studies of a semi‐automated separation method for analysis of non‐ortho substituted polychlorinated biphenyl (PCB) congeners in environmental samples

Non‐ortho substituted polychlorinated biphenyl (PCB) congeners can account for the majority of the dioxin‐like toxicity in environmental samples, yet analysis for these congeners is difficult because other PCB congeners co‐elute with them in most Chromatographic methods. An automated method was developed which incorporates a porous graphitic carbon (PGC) column which is commercially available. Non‐ortho substituted congeners were successfully separated from interfering PCB congeners. Recoveries of non‐ortho substituted congeners were consistently reproducible (CV < 9%) when chicken eggs were fortified with individual congeners.