Headspace solid-phase microextraction in combination with gas chromatography and tandem mass spectrometry for the determination of organochlorine and organophosphorus pesticides in whole numan blood

A method for the determination of several organochlorine and organophosphorus pesticides in human whole blood samples was developed. The combination of solid-phase microextraction in headspace mode with gas chromatography with tandem mass spectrometry allowed the determination of 11 selected pesticides at ppb levels, minimizing the sample treatment. Quantitation was carried out by means of calibration curves prepared in blood using labelled surrogate/internal standards. The method showed good linearity between 1 and 50 ng ml(-1) (0.5-25 ng ml(-1) for HCB) using second-order calibration curves. Precision was found to be better than 20% at the three concentration levels assayed in the range of ng ml(-1). The detection limits obtained were in the range 0.02-0.7 ng ml(-1), except for p,p'-DDT (3 ng ml(-1)). The developed procedure was applied to blood and serum samples obtained from agricultural workers. HCB. beta-HCH and p,p'-DDE were most frequently detected in the samples analyzed.     

High throughput method for the determination of organochlorine pesticides and polychlorinated biphenyls in human serum

An improved method for the determination of selected organochlorine pesticides (OCPs) and polychlorinated biphenyls (PCBs) in human serum was developed. The method requires low volume of serum (500 microl) and 48-96 samples per day can be prepared by one analyst without special automatic equipment. Initial extraction was performed using 96-well solid-phase extraction disk plates and was followed by a clean-up with silica gel/sulfuric acid. Different denaturation, elution and clean-up conditions were tested. Quantification was carried out by gas chromatography equipped with electron capture detector (GC-ECD) or mass spectrometer (GC-MS). Recoveries of PCB congeners 28, 52, 101, 118, 138, 153 and 180 and OCPs HCB, beta-HCH, p,p'-DDE and p,p'-DDT at two spiking levels (n=8) varied from 57 to 120%, and intra-day relative standard deviation from 1 to 11%, both depending on spiking level and compound. Inter-day relative standard deviation was <15% in all cases. Limit of quantification (LOQ) for these PCBs ranged from 0.08 to 0.13 ng/ml and for these OCPs from 0.16 to 0.40 ng/ml. The optimized method was applied to the analysis of 1000 serum samples from different places of Spain.     

Distribution,Sources Identification,and Ecological Risk of PAHs and PCBs in Coastal Surface Sediments from the Northern Persian Gulf

Hormozgan Province plays a vital role in fishery, petroleum, and industrial activities in southern Iran. However, no comprehensive studies on organic pollution have been performed. PCBs and PAHs were analyzed in surface sediments from areas receiving industrial (nine sites), river (one site), and urban (two sites) effluents. The sediment samples were collected in March and September 2010 (in dry and wet seasons) at the highest tidal time. The overall pollution level of PCBs ranged from 2.5 ± 0.8 to 462.0 ± 206.7 ng/g dry weight. CB153 congener dominated in most of the sediment samples. Congener profiles of PCBs showed close similarity with formulations of commercial products such as Aroclor 1260 and 1254 g. A wide range of 55.3 to 1231.6 ng/g dry weight was detected for ∑PAHs. Results of PCA and PCA-MLR tests confirmed both petrogenic and pyrogenic origins for PAH pollution. The higher means of ∑PAHs and ∑PCBs in industrial and urban wastewaters were found near the shore, evidencing the role of these wastewaters in the PAH and PCB contamination in Hormozgan sediment. The concentrations of PAHs and PCBs in detected hotspots exceed the U.S. NOAA sediment quality guidelines.     

宁波滩涂贝类养殖区沉积物中有机氯农药和多氯联苯残留及生态风险评估

利用GC-ECD对宁波市主要滩涂贝类养殖区表层沉积物中的多氯联苯(PCBs)和有机氯农药六六六(HCHs)、滴滴涕(DDTs)的残留量进行测定,研究其分布状况,并进行生态风险评估.结果表明:贝类养殖区表层沉积物中的总有机氯农药含量为0.80～32.40ng·g-1,多氯联苯含量为3.20～33.33 ng·g-1.HCHs主要来自远距离大气传输及历史残留,部分区域有DDTs输入,其来源可能是三氯杀螨醇的使用.大部分站位的p,p’-DDT和DDTs存在潜在的生态风险,其中墙头和西店海域的p,p’-DDT残留超过生物效应中值,对底栖生物毒害效应较高.大多数站位PCBs的生态风险较低.     

Geographic variation of PCB congeners in polar bears (Ursus maritimus) from Svalbard east to the Chukchi Sea

We present data on geographic variation in polychlorinated biphenyl (PCB) congeners in adult female polar bears (Ursus maritimus) from Svalbard eastward to the Chukchi Sea. Blood samples from 90 free-living polar bears were collected in 1987-1995. Six PCB congeners, penta to octa chlorinated (PCB-99, -118, -153, -156, -180, -194), were selected for this study. Differences between areas were found in PCB levels and congener patterns. Bears from Franz Josef Land (11,194 ng/g lipid weight) and the Kara Sea (9,412 ng/g lw) had similar DPCB levels and were higher than all other populations (Svalbard 5,043 ng/g lw, East Siberian Sea 3,564 ng/g lw, Chukchi Sea 2,465 ng/g lw). Svalbard PCB levels were higher than those from the Chukchi Sea. Our results, combined with earlier findings, indicate that polar bears from Franz Josef Land and the Kara Sea have the highest PCB levels in the Arctic. Decreasing trends were seen eastwards and westwards from this region. Of the congeners investigated in the present study, the lower chlorinated PCBs are increasing and the high chlorinated PCBs are decreasing from Svalbard eastward to the Chukchi Sea. Different pollution sources, compound transport patterns and regional prey differences could explain the variation in PCB congener levels and patterns between regions.     

Persistent toxic substances in the muscles and liver of the pacific walrus Odobenus rosmarus divergens Illiger, 1815 from the Bering Sea

This study reports data on the contents of organochlorine pesticides and heavy metals in the muscles and livers of eight individuals (five males and three females) of the Pacific walrus Odobenus rosmarus divergens Illiger, 1815, which were captured in the summer of 2011 in Mechigmensky Bay of the Bering Sea. Pesticides, namely α-, β-, and γ-isomers of hexachlorocyclohexane (HCH), dichlorodiphenyltrichloroethane (DDT) and its metabolites dichlorodiphenyldichloroethane (DDD) and dichlorodiphenyldichloroethylene (DDE), as well as the heavy metals Cd, Pb, and Hg were found in all samples studied. The total concentration of organochlorine pesticides in the muscles varied from 200 to 5700 ng/g lipid weight and in the liver from 4900 to 90300 ng/g lipid weight. The concentrations of cadmium, lead, and mercury were 0.04–6.7, 0.13–0.76, and 0.03–0.40 μg/g dry weight, respectively. On the whole, the contents of organochlorine pesticides and heavy metals in the organs of the Pacific walrus were lower compared to those in marine mammals from other regions of the World Ocean.     

Organochlorine contaminants in freshwater mussels; occurrence,bioaccumulation pattern,spatio-temporal distribution and human health risk assessment from the tributaries of River Ravi,Pakistan

The present study was conducted to investigate the bioavailable levels and human health risk of organochlorine contaminants (OCs), particularly organochlorine pesticides (OCPs) and polychlorinated biphenyls (PCBs) in freshwater mussels from northern three tributaries of River Ravi, Pakistan that provides the pioneer data for the occurrence of POPs in the freshwater mussels from Pakistan. The Σ₂₃OCPs and Σ₃₅PCBs concentrations in mussels were ranged from 189.66–2049.40 ng/g and 25.81 to 135.38 ng/g, respectively. The comparison of current bioavailable levels of OCs with maximum residual limits (MRLs) established by Food and Agricultural Organization and European Union revealed that Σendosulfan (100%), ΣDDTs (93%), HCB (87%), β-HCH (77%), endrin (77%), γ-HCH (70%), heptachlor (67%), aldrin (67%), dielrin (67%), Chlordane (70%), α-HCH (40%), and WHO-TEQ (2005) values for PCB-126, PCB-169 and Σ₈DL-PCBs were exceeding the permissible limits. The human health risk assessment revealed the occurrence of substantial lifetime carcinogenic risk for OCPs and PCBs at both 50th and 95th percentile concentrations in freshwater mussels from the tributaries of River Ravi. Therefore, the freshwater mussels are recommended to be used in environmental toxicological studies to assess the bioavailable levels of pollution in hostile environment.     

太湖湿地生态系统有机氯污染的夜鹭生物指示

1999年春季,在对无锡鼋头渚鹭鸟种群野外生态调查的基础上,对夜鹭幼鸟反吐物,觅食地底泥和水体进行了采样,并在实验室用气相色谱测定了样品中的α-HCH、β-HCH、γ-HCH、艾氏剂、狄氏剂、异狄氏剂、七氯、环氧七氯、p,p'-DDE、p,p'-DDD、o,p'-DDT和p,p'-DDT等有机氯农药的残留状况,结果表明,在有机氯农药禁用近20年后,六六六的异构体和滴滴涕及其衍生物均能在环境中和夜鹭食物中有不明,在有机氯农药禁用近20年后,六六六的异构体和滴滴涕及其衍生物均能在环境中和夜鹭食物中有不明,在有机氯农药禁用近20年后,六六六的异构体和滴滴涕及其衍生物均能在环境中和夜鹭食物中有不检出,有机氯污染物沿夜鹭食物链产生逐级富集,太湖湿地生态系统中夜鹭卵富集了滴滴涕万倍以上,富集了六六六数千倍,从而使有机氯污染物易被检测,因此夜鹭锘放可作为湿地生态系统有机氯污染的生物指示物。     

Estimation of the load of cyclic organochlorines in North Sea zooplankton

During a North Sea survey in late spring 1986, zooplankton biomass (g dry weight/m²) as well as pollutant concentrations in zooplankton (ng/g dry weight) were determined at 127 stations. On the basis of these data, the load of several cyclic organochlorines in zooplankton (ng/m²) was estimated. It appeared that the highest loads of these pollutants were incorporated in the large zooplankton stocks of the northern and central North Sea, north of 56°N, whereas the highest concentrations were found in zooplankton of the southern North Sea. An explanation for the accumulation of pollutants in sediments as well as in benthos organisms of the central and northern North Sea as found by several authors is discussed in connection with the assumption of a considerably high vertical flux of organic material in these areas. The calculation of total zooplankton content in the North Sea during the late spring survey amounted to about 5 million tons dry weight. This biomass was estimated to contain about 2.6 t PCBs, 19.3 kg p,p′-DDE, 12 kg τ-HCH, 6.4 kg HCB und 5.6 kg α-HCH. These results agree with those on other compartments of the North Sea ecosystem (benthos, fish) found in recent literature. The estimated annual turnover of PCBs in zooplankton (15.2 t) is of the same order of magnitude as the estimated amount transported yearly into the North Sea by rivers and the atmosphere (6–13 t).     

PAHs,OCPs and PCBs in sediments from three catchments in Durban,South Africa

Polycyclic aromatic hydrocarbons (PAHs), organochlorine pesticides (OCPs) and polychlorinated biphenyls (PCBs) were analysed from sediment samples collected in 2012 from rivers, surface runoff canals and estuaries in three highly urbanised catchments in durban, KwaZulu-Natal, South Africa. PAHs were ubiquitous, at concentrations between 36–6 800 ng g^?1 dry mass (dm). Congener ratio diagnosis suggests the PAHs were derived predominantly from pyrogenic sources. Four OCPs and/or their metabolites were detected at varying frequencies and concentrations. Of these, dichlorodiphenyltrichloroethane (ddT) and metabolites were most frequently detected and were at a high concentration in sediment in some systems. Toxaphene was detected at a high concentration at some sites. The total PCB concentration varied widely, from below the method detection limit to 110 ng g^?1 (dm). Based on the comparison of chemical concentrations to international sediment quality guidelines, PAH, OCP and PCB concentrations in most sediment samples posed a low risk to sediment-dwelling organisms. However, in some instances the risk was moderate or high. It is recommended that these compounds be monitored more frequently and comprehensively in aquatic ecosystems to better understand the ecological and human health implications.     

The impact of the marine sewage outfalls on the sediment quality: The Black Sea and the Marmara case

Marine sewage outfalls are the cheapest method of disposal for municipalities with restricted funds, despite their negative effects on marine ecosystems. This study was conducted on the marine sewage outfalls of the Turkish cities Rize (Black Sea) and Yalova (Sea of Marmara). Heavy metals, polycyclic aromatic hydrocarbons (PAHs), polychlorinated biphenyls (PCBs), and organochlorine pesticides (OCPs) were investigated in the sediments for determine pollution degree. Two of Yalova stations were classified as having high contamination levels (1034.436 and 1476.483 ng/g, respectively) and all the other stations suffered moderate pollution in terms of ∑₁₆PAHs. ∑DTTs in sediments above probable effect levels (PELs), were observed both stations Yalova and Rize. The highest metal concentrations in the sediments from the eight stations ranged from 4.97 to 29.65 mg/kg for Ni; 7.57–44.14 mg/kg for Cr; 9.84–42.76 mg/kg for Cu; and 48.08–103.77 mg/kg for Zn. In sum, examination of pollutant sources provides clear evidence of an anthropogenic effect on the discharge environments.     

Distribution of organochlorines and ecological risks in surface sediments from El-Mex Bay,Mediterranean Sea

Polychlorinated biphenyls (PCBs) and organochlorine pesticides (OCPs) were determined in eight sampling sites collected from El-Mex Bay sediments during the period of 2013–2015. Concentrations of PCBs, Hexachlorocyclohexanes (HCHs), Dichloro Diphenyl Trichloroethanes (DDTs), and cyclodienes ranged from 0.148 to 23.99, ND to 0.089, ND to 4.64, and 0.005 to 0.581 ng g^?1 dry wt, respectively. Total organic carbon (TOC) was relatively low, ranging from 0.09% to 1.42%. Total carbonate content ranged from 38% to 58%. The negative correlation of TOC with total pesticides (r = ?0.18) suggested that TOC does not have a role binding with pesticides. On the other hand, a positive correlation between PCBs and TOC (r = 0.254 at p > 0.01) was observed probably due to the low solubility of PCBs in the seawater. So, it will continue to precipitate until it reaches the bottom water and contaminates the sediment. The data obtained in the present work compared well with the counterpart data reported internationally. In general, the results of PCBs and OCP concentrations in El-Mex Bay sediments were much lower than the permissible levels recorded by sediment quality guidelines (SQGs). Interestingly, the organochlorines in sediments of El-Mex Bay were below the respective SQG values and were not likely to pose potential biological adverse impact.     

Further mutagenicity studies on pesticides in bacterial reversion assay systems

A total of 228 pesticides (88 insecticides, 60 fungicides, 62 herbicides, 12 plant-growth regulators, 3 metabolites and 3 other compounds) was tested for mutagenicity in bacterial reversion-assay systems with 5 strains (TA100, TA98, TA1535, TA1537 and TA1538) of Salmonella typhimurium and a strain (WP2 hcr) of Escherichia coli. 50 pesticides (25 insecticides, 20 fungicides, 3 herbicides, 1 plant-growth regulator and 1 other compound) were found to be mutagenic. 5 of them required metabolic activation (S9 mix) for their activities. Among various chemical groups, organic phosphates, halogenated alkanes and dithiocarbamates showed higher ratios of mutagens. Although 22 of the pesticides tested have been reported to be carcinogenic, 7 of them, i.e., captain, DBCP, EDB, EDC, ETU, HEH and nitrofen, were detected as mutagens in the present assay. Most of the other 15 non-mutagenic carcinogens were organochlorine pesticides such as alpha-BHC, chlorobenzilate, p,p'-DDT, dieldrin and quintozene.     

PCB concentrations in sediments from the Gulf of Nicoya estuary, Pacific coast of Costa Rica

Thirty-one sediment samples collected from 1996-2003 from the Gulf of Nicoya estuary on the northwestern coast of Costa Rica, have been obtained for PCB analyses. This is part of the first study to evaluate the PCB contamination in coastal Costa Rica. Overall, the concentrations are low, especially when compared to sediments from more temperate climates and/or sediments from more heavily industrialized areas. Values average less than 3 ng/g dw sediment, however, a few samples contained up to 7 ng/g dw sediment. Sediments with the highest concentrations were located in the Punta Morales area, where muds were sampled from among mangrove roots. The Puntarenas samples had surprisingly low PCB concentrations, likely due to their sandy lithology. The congener distribution within the majority of the samples showed signs of either recent sources or lack of degradation. However, a few sites, specifically some of the inter-gulf islands and more remote samples had congener distributions indicative of airborne contaminants and/or degradation. Considering the presence of airborne PCBs in the Gulf of Papagayo to the north, the lack of airborne PCBs and more varied congener distribution in the Gulf of Nicoya estuary was surprising.     

Occurrence,distribution and transport of pesticides into the Salton Sea Basin,California, 2001–2002

The Salton Sea is a hypersaline lake located in southeastern California. Concerns over the ecological impacts of sediment quality and potential human exposure to dust emissions from exposed lakebed sediments resulting from anticipated shrinking of shoreline led to a study of pesticide distribution and transport within the Salton Sea Basin, California, in 2001–2002. Three sampling stations—upriver, river mouth, and offshore—were established along each of the three major rivers that discharge into the Salton Sea. Large-volume water samples were collected for analysis of pesticides in water and suspended sediments at the nine sampling stations. Samples of the bottom sediment were also collected at each site for pesticide analysis. Sampling occurred in October 2001, March–April 2002, and October 2002, coinciding with the regional fall and spring peaks in pesticide use in the heavily agricultural watershed. Fourteen current-use pesticides were detected in water and the majority of dissolved concentrations ranged from the limits of detection to 151 ng/l. Diazinon, EPTC and malathion were detected at much higher concentrations (940–3,830 ng/l) at the New and Alamo River upriver and near-shore stations. Concentrations of carbaryl, dacthal, diazinon, and EPTC were higher in the two fall sampling periods, whereas concentrations of atrazine, carbofuran, and trifluralin were higher during the spring, which matched seasonal use patterns of these pesticides. Current-use pesticides were also detected on suspended and bed sediments in concentrations ranging from detection limits to 106 ng/g. Chlorpyrifos, dacthal, EPTC, trifluralin, and DDE were the most frequently detected pesticides on sediments from all three rivers. The number of detections and concentrations of suspended sediment-associated pesticides were often similar for the river upriver and near-shore sites, consistent with downstream transport of pesticides via suspended sediment. While detectable suspended sediment pesticide concentrations were more sporadic than detected aqueous concentrations, seasonal trends were similar to those for dissolved concentrations. Generally, the pesticides detected on suspended sediments were the same as those on the bed sediments, and concentrations were similar, especially at the Alamo River upriver site. With a few exceptions, pesticides were not detected in suspended or bed sediments from the off-shore sites. The partitioning of pesticides between water and sediment was not predictable from solely the physical–chemical properties of individual pesticide compounds, but appear to be a complicated function of the quantity of pesticide applied in the watershed, residence time of sediments in the water, and compound solubility and hydrophobicity. Sediment concentrations of most pesticides were found to be 100–1,000 times lower than the low-effects levels determined in human health risk assessment studies. However, maximum concentrations of chlorpyrifos on suspended sediments were approximately half the low-effects level, suggesting the need for further sediment characterization of lake sediments proximate to riverine inputs. Guest editor: S. H. Hurlbert The Salton Sea Centennial Symposium. Proceedings of a Symposium Celebrating a Century of Symbiosis Among Agriculture, Wildlife and People, 1905–2005, held in San Diego, California, USA, March 2005     

Induction of micronuclei in vitro by organochlorine compounds in beluga whale skin fibroblasts

Beluga whales (Delphinapterus leucas) inhabiting the St. Lawrence estuary are highly contaminated with environmental pollutants and have a high incidence of cancer. Environmental contaminants may be partly responsible for the high cancer incidence observed in this population. DNA damage plays an important role in the development of cancer. The micronuclei (MN) assay was used to test the genotoxic potential of organochlorine (OC) pesticides with and without external metabolic factor in skin fibroblasts of an Arctic beluga whale. Toxaphene, chlordane and p,p'-DDT induced significant (p<0. 05) concentration-response increases of micronucleated cells (MNCs). Statistically significant increases in MNCs, ranging from 1.7- to 5-folds when compared to control cultures, were observed for 0.05, 0. 5, 5 and 10 microg/ml toxaphene, 2, 5 and 10 microg/ml chlordane and 10 and 15 microg/ml p,p'-DDT. Presence of exogeneous metabolic factor (S9) completely abolished the MN induction potency of chlordane and p,p'-DDT, and toxaphene induced MN formation at higher concentrations (0.5 microg/ml) than without S9 mix. The ecotoxicological significance of MN induction by low concentrations of toxaphene is unknown and do not imply that toxaphene is involved in the etiology of cancer in St. Lawrence beluga whales. However, because of the known genotoxicity of toxaphene and the long lifespan of beluga whales, it cannot be excluded that toxaphene may pose a long-term genetic hazard to the more contaminated whales of this population.     

Relationships between tissue contaminant concentrations in a small sample of seabirds

1. The metal and organochlorine contaminant concentrations were measured in a small sample of three seabird species collected from St Kilda, Scotland, UK, and the relationship between concentrations of different contaminants within and between tissues was compared. 2. There was little evidence that the concentration of a contaminant in one tissue was indicative of the concentration in any other tissue. 3. Generally, different contaminants had not co-accumulated in tissues; this was so even for the lipophilic compounds (DDE and PCBs), with the exception of puffin fat. 4. There was a tendency for the species containing the most fat to contain the highest concentrations of lipophilic contaminants and there was some suggestion that the fat in muscle could play a role in determining PCB concentrations.     

Seasonal-spatial distributions,congener profile,and risk assessment of polychlorinated biphenyls (PCBS) in the surficial sediments from the coastal area of Bangladesh

A comprehensive congener specific assessment of polychlorinated biphenyls (PCBs) was conducted for the first time in Bangladesh. All 209 PCB congeners in the surficial coastal sediments from the coastal areas of Bangladesh were analyzed by GC-MS/MS. The total concentrations of PCBs (∑PCBs) varied from 5.27 to 92.21 and 4.61 to 105.3 ng/g dw in winter and summer, respectively, and the ranges were comparable to or higher than those recorded in the sediments from the coastal areas of India, Korea, China, and Taiwan. The seasonal difference in the levels of PCBs was not statistically significant (p > 0.05). The spatial distribution revealed that the areas with recent urbanization and industrialization (Chittagong, Cox’s Bazar and Sundarbans) were more contaminated with PCBs than the unindustrialized area (Meghna Estuary). Moderately chlorinated (4–6 Cl) homologs dominated PCB profiles. A set of congeners based on their detection frequencies and abundance were identified and categorized as potential environmental marker PCBs, which can be used for the future selective monitoring studies where there would be limitations on whole congener assessment. Ecotoxicologically, the sedimentary PCB concentrations exceeded some of the existing environmental quality standards, suggesting a potential threat to the aquatic organisms in the Bangladeshi coastal areas.     

Automated solid-phase extraction for the determination of polybrominated diphenyl ethers and polychlorinated biphenyls in serum--application on archived Norwegian samples from 1977 to 2003

An analytical method comprised of automated solid-phase extraction and determination using gas chromatography mass spectrometry (single quadrupole) has been developed for the determination of 12 polybrominated diphenyl ethers (PBDEs), 26 polychlorinated biphenyls (PCBs), two organochlorine compounds (OCs) (hexachlorobenzene and octachlorostyrene) and two brominated phenols (pentabromophenol, and tetrabromobisphenol-A (TBBP-A)). The analytes were extracted using a sorbent of polystyrene-divinylbenzene and an additional clean-up was performed on a sulphuric acid-silica column to remove lipids. The method has been validated by spiking horse serum at five levels. The mean accuracy given as recovery relative to internal standards was 95%, 99%, 93% and 109% for the PBDEs PCBs, OCs and brominated phenols, respectively. The mean repeatability given as RSDs was respectively 6.9%, 8.7%, 7.5% and 15%. Estimated limits of detection (S/N=3) were in the range 0.2-1.8 pg/g serum for the PBDEs and phenols, and from 0.1 pg/g to 56 pg/g serum for the PCBs and OCs. The validated method has been used to investigate the levels of PBDEs and PCBs in 21 pooled serum samples from the general Norwegian population. In serum from men (age 40-50 years) the sum of seven PBDE congeners (IUPAC No. 28, 47, 99, 100, 153, 154 and 183) increased from 1977 (0.5 ng/g lipids) to 1998 (4.8 ng/g lipids). From 1999 to 2003 the concentration of PBDEs seems to have stabilised. On the other hand, the sum of five PCBs (IUPAC No. 101, 118, 138, 153 and 180) in these samples decreased steadily from 1977 (666 ng/g lipids) to 2003 (176 ng/g lipids). Tetrabromobisphenol-A and BDE-209 were detected in almost all samples, but no similar temporal trends to that seen for the PBDEs were observed for these compounds, which might be due to the short half-lives of these brominated flame retardants (FR) in humans.     

Organochlorine pesticides in Cyprinus carpio from Sidi Salem Dam,north-western Tunisia

Cyprinus carpio (Linnaeus, 1758) caught in Sidi Salem Dam in 2011 were analysed for the levels of organochlorine pesticides (OCPs), including hexachlorobenzene (HCB), aldrin, heptachlor, lindane, dieldrin, endrin, and pp′-DDT and its two main metabolites pp′-DDD and pp′-DDE, in order to evaluate the extent of contamination of the dam. Fish were sampled monthly within the dam during 2011. Muscle, liver and gill tissues were analysed by gas chromatography for the determination of OCPs. Samples had variable concentrations of OCPs, ranging from 2.26 to 17.93 ng g?1, 0.59 to 42.67 ng g?1 and 3.30 to 84.27 ng g?1, which were isolated from gills, muscle and liver, respectively. The organochlorine pesticide levels found posed no threat to human health. The highest OCP levels were found in the liver tissues. The pp′-DDE concentrations and their ratios to ΣDDTs indicate aged DDT pollution and suggests that there has been no recent input of technical DDT from the agricultural areas into Sidi Salem Dam.