Organochlorine pesticides in colostrums in case of normal and preterm labor (IASI, Romania)

Assessment of organochlorine pesticides (OCPs) in human body is important for human health because they have weak estrogenic or antiestrogenic effects and are considered endocrine disrupters. We used colostrum of women as indicator for levels of OCPs in human body for mothers with normal and preterm labor from eastern part of Romania. Sixty- three samples of colostrum were extracted by solid-phase extraction. Analyses were carried out using gas chromatography coupled to mass spectrometry (GC-MS). OCPs have been detected in all samples, with p,p’-dichlorodiphenyldichloroethylene (p,p’-DDE) and γ-hexachlorocyclohexane (γ-HCH) being at the highest concentrations. Of the organochlorines measured in clostrum samples from women in preterm labor, median levels of DDTs (470 ng/g) and HCHs (99 ng/g) were higher than for the same compounds from women in normal labor (median of DDTs = 268 ng/g and median of HCHs = 96 ng/g). Normal labor had higher median concentrations of HCB (19.5 ng/g) versus preterm labor (14 ng/g). Statistical data show high Spearman correlation coefficients between various OCPs. We found a good correlation between α-, γ-, β- and δ- HCH isomers (p < 0.001) for both normal and preterm labor. The most abundant target compound was p,p’-DDE (median value 96 ng/g, and 137 ng/g for mother with normal and preterm labor, respectively) in all colostrum samples. The estimated daily intakes of HCHs by infants exceeded corresponding Health Canada guidelines.     

Geography and stage of development affect persistent organic pollutants in stranded and wild-caught harbor seal pups from central California

Persistent organic pollutants have been associated with disease susceptibility and decreased immunity in marine mammals. Concentrations of polychlorinated biphenyls (PCBs), dichlorodiphenyltrichloroethane and its metabolites (DDTs), polybrominated diphenyl ethers (PBDEs), chlordanes (CHLDs), and hexachlorocyclohexane isomers (HCHs) were evaluated in terms of stage of development and likely exposure routes (in utero, suckling, fasting) in the blubber of 202 stranded and wild-caught, primarily young of the year (n = 177), harbor seals (Phoca vitulina) in the central California coast. This is the first report of HCH concentrations in the blubber of California seals. Lipid normalized concentrations ranged from 200 to 330,000 ng/g for sum PCBs, 320-1,500,000 ng/g for sum DDTs, 23-63,000 ng/g for sum PBDEs, 29-29,000 ng/g for sum CHLDs, and 2-780 ng/g for sum HCHs. The highest concentrations were observed in harbor seal pups that suckled in the wild and then lost mass during the post-weaning fast. Among the pups sampled in the wild and those released from rehabilitation, there were no differences in mass, blubber depth, or percent lipid although contaminant concentrations were significantly higher in the pups which nursed in the wild. When geographic differences were evaluated in a subset of newborn animals collected near their birth locations, the ratio of sum DDTs to sum PCBs was significantly greater in samples from an area with agricultural inputs (Monterey), than one with industrial inputs (San Francisco Bay). A principal components analysis distinguished between seals from San Francisco Bay and Monterey Bay based on specific PCB and PBDE congeners and DDT metabolites. These data illustrate the important influence of life stage, nutritional status, and location on blubber contaminant levels, and thus the need to consider these factors when interpreting single sample measurements in marine mammals.     

Assessment of organochlorine pesticides in human milk and risk exposure to infants from North-East India

Despite the worldwide ban on use of persistent organochlorine pesticides, their usage continued until recently in India, for vector-borne disease eradication programs and agricultural purposes. The concentrations of organochlorine contaminants, DDT and HCH, have been determined in human breast milk from Dibrugarh and Nagaon districts of Assam state, North-East India. The results demonstrated that the mean levels of total DDT were 3210 ng/g lipid wt. and 2870 ng/g lipid wt. and total HCH were 2720 ng/g lipid wt. and 2330 ng/g lipid wt. in Nagaon and Dibrugarh respectively. There was no significant difference in the levels of investigated pollutants between the two districts. Significant differences in ADI (Average daily intake) for total DDT were found between the two districts. In addition, a positive correlation was observed between OCP levels in breast milk and age of mothers. Based on OCP levels in human breast milk, the ADI by the infants has been estimated. It has been found that high daily intake of DDTs and HCHs by the infants exceeded the TDI (Tolerable daily intake) which implied that infants of the region are potentially at high risk by these contaminants.     

Levels of chlorinated pesticides and polychlorinated biphenyls in Norwegian breast milk (2002-2006), and factors that may predict the level of contamination

In the present study, polychlorinated biphenyls (PCBs) and organochlorine pesticides (OCPs) were determined in 423 breast milk samples from women living in Norway. Various predictors for the contaminant levels were also investigated. The samples were collected in six counties, representing South, Central and North Norway in 2002-2006. Initial results showed significantly lower levels of OCPs in breast milk from ethnic Norwegians (N = 377) compared to ethnic non-Norwegians (N = 46). Median concentrations (range) of PCBs, p,p′-DDE, HCB, β-HCH and oxychlordane in breast milk of the Norwegian women, all parities included, were 103 (34-450), 41 (5.4-492), 11 (3.6-24), 4.7 (0.9-37) and 2.8 (0.5-16) ng/g lipid weight, respectively. Results indicated that sum of 18 PCBs, p,p′-DDE and β-HCH are good predictors for monitoring of PCB, DDT and HCH levels in Norwegian breast milk. Multivariable linear regression analyses showed that age was strongly associated with increasing OC levels (P < 0.001), whereas parity was associated with decreasing OC levels (P < 0.001). Smoking was associated with higher levels of PCBs, p,p′-DDE and β-HCH. The models explained from 17 to 35% of the variance. Median levels of OCs in the present Norwegian primparaes seemed to be 29-62% lower than corresponding results found in a Norwegian study from 2000-2002.     

Levels and patterns of Persistent Organic Pollutants (POPS) in selected food items from Northwest Russia (1998-2002) and implications for dietary exposure

Residues of persistent organic pollutants (POPs) were analysed in 70 selected food items from Northwest Russia in 1998-2002. Levels of PCBs ranged from 0.2 to 16 ng/g wet weight (ww) in dairy products and fats, 0.2 to 23 ng/g ww in meat products, 0.5 to 16 ng/g ww in eggs and 0.3 to 30 ng/g ww in fish. High levels of DDT (16 ng/g ww) were found in locally produced butter from Kola Peninsula, in pork fat from Arkhangels region (10 to 130 ng/g ww) and in some fish samples from White Sea and Kargopol region (17 and 30 ng/g ww). Findings of low DDE/DDT ratios in many of the studied food items indicated recent contamination to DDTs. Mean levels of sum TEQs_WHO1998 of dioxin-like mono-ortho PCBs: PCBs 105, 118, 156 and 157 (∑ mo-PCBs-TEQs_WHO1998) were highest in dairy products, chicken eggs and fish, with levels of 0.292, 0.245 and 0.254 pg/g ww, respectively. The estimated daily intake (EDI) for ∑ mo-PCBs-TEQs_WHO1998 was 0.74 pg/kgbw/day and in the same range as in Sweden and Denmark. Fish, dairy products, eggs and meat were the main contributors to the EDI of ∑ mo-PCBs-TEQs_WHO1998. The EDIs of DDTs, HCHs and HCB were several times higher than in Sweden and Denmark. Consumption of meat and poultry were important sources for intake of DDTs and HCHs, respectively. Contamination of animal feed and agricultural practice were assumed the most important causes for the results in the present study. However, increased control on maximum residue levels in food and feed may have resulted in large changes on levels and patterns of POPs in food in the studied areas.     

Organochlorines and mercury in livers of great cormorants (Phalacrocorax carbo sinensis) wintering in northeastern Mediterranean wetlands in relation to area, bird age, and gender

Wild birds are exposed to pollutants in their habitats. Top consumers of aquatic environments such as the fish-eating great cormorant (Phalacrocorax carbo sinensis) are especially affected due to the bioaccumulation of toxic substances in their tissues. This study analysed the livers of 80 great cormorants from Greece to estimate the concentration of organochlorines and mercury and to examine their possible toxic effects and origin. The results showed that mercury (geometric mean 8089 ng g⁻¹ dw), p,p′-DDE (2628 ng g⁻¹ dw), ∑ HCHs (47 ng g⁻¹ dw) and HCB (116 ng g⁻¹ dw) concentrations can be considered high compared with those found in great cormorant livers elsewhere except in highly polluted areas, whereas ∑ PCBs occurred in relatively low concentrations (1091 ng g⁻¹ dw). β-HCH was the dominant HCH isomer. Pollutant levels were generally unrelated to area, age and gender. However, p,p′-DDE and p,p′-DDD showed intersite differences, whilst the proportion of PCBs with 8 chlorine atoms were significantly higher in adult than 1st year great cormorants. Pollution did not reflect local patterns but rather these along the Baltic and Black Seas, whilst differences in p,p′-DDE concentration and ∑ DDTs/∑PCBs ratios between Evros, Axios or Amvrakikos, found on common migration route, suggested different bird origins. Most birds had toxic mercury concentrations; 83.7% above 4000 ng g⁻¹ dw and 16% above 17,000 ng g⁻¹ dw. Other pollutant levels were too low to have adverse effects.     

Levels of brominated flame retardants and other pesistent organic pollutants in breast milk samples from Limpopo Province, South Africa

The non-occupational exposure to brominated flame retardants, and other persistent organic pollutants (POPs) was studied by collecting human breast milk samples from mothers residing in Thohoyandou area, a rural district in the Limpopo Province, northern part of South Africa (SA). Of all collected samples to be analysed (n = 28), those with large enough milk volumes, (n = 14) were quantified for polybrominated diphenyl ethers (PBDEs) (9 congeners: BDE-28, 47, 66, 99, 100, 138, 153, 154, and 183) and hexabromocyclododecane (HBCD) on a GC equipped with dual capillary columns and dual electron-capture detectors (ECD). The levels of PBDE congeners (median sumBDE 1.3 ng/g of lipids) and of HBCD were not far from levels generally found in European studies, and this study may be the first report on the presence of PBDEs and HBCD in SA breast milk. On a congener basis, the finding of comparably high BDE-183 levels suggests a specific PBDE usage, or contamination situation in SA. Apart from BFRs, the high DDT levels found in the breast milk from this area (median and maximum sumDDT levels of about 4 600 and over 20 000 ng/g of lipids, respectively; n = 28) have earlier been reported. In addition, other POPs (PCBs, HCB and HCHs) were found in SA breast milk, at relatively low levels. To conclude, measurable levels of PBDEs and HBCD, and a specific BDE congener pattern, were found in breast milk from the Limpopo province, SA. A number of other POPs, including DDTs in high levels, were also present.     

In vitro steroidogenic effects of mixtures of persistent organic pollutants (POPs) extracted from burbot (Lota lota) caught in two Norwegian lakes

This study investigated the effects of two mixtures of persistent organic pollutants (POPs) on steroidogenesis in the H295R cell line. The two mixtures were obtained from the livers of burbot (Lota lota) caught in two Norwegian lakes (Mjøsa and Losna) with different contaminant profiles. Steroid hormone levels in the cell culture medium and mRNA levels of 16 genes involved in steroidogenesis were investigated. The crude Lake Mjøsa extract had to be diluted ten times more than the Lake Losna extract in order to prevent cytotoxicity. The ten times diluted Lake Mjøsa mixture had higher levels of DDT and derivates (∑ DDTs, 1.7 times) and brominated flame retardants (∑ BDEs and HBCD, 15-25 times) than the Lake Losna mixture, which, on the other hand, had higher concentrations of ∑ PCBs (1.5 times higher) and also of HCB, ∑ HCH isomers and ∑ chlordane isomers (5-20 times higher).In the cell culture media, only cortisol levels were increased at the highest exposure concentration to the Lake Mjøsa mixture, while both cortisol and estradiol levels were increased following exposure to the two highest Lake Losna mixture exposure concentrations. Testosterone levels decreased only at the highest exposure concentration of the Lake Losna mixture. Multivariate models suggested that ∑ PCBs, and to a lesser extent ∑ DDTs, were responsible for the cortisol responses, while estradiol and testosterone alterations were best explained by HCB and ∑ PCBs, respectively. Exposure to the mixtures generally increased mRNA levels, with smaller effects exerted by the Lake Mjøsa mixture than the Lake Losna mixture. It was concluded that both mixtures affected steroidogenesis in the H295R cells. Small differences in mixture composition, rather than the high content of brominated flame retardants in the Lake Mjøsa mixture, were suggested to be the most probable reason for the apparent differences in potencies of the two mixtures.     

Analysis of composition, distribution and origin of hexachlorocyclohexane residues in agricultural soils from NW Spain

Concentrations of the isomers of the organochlorine pesticide hexachlorocyclohexane (HCH) were determined in 252 surface soil samples collected within a sampling network covering agricultural areas in Galicia (NW Spain). The concentration of total HCH (sum of α + β + γ + δ) ranged between 4 and 2305 ng g⁻¹ (dry weight), with the α-HCH and γ-HCH isomers predominating (< 1-1404 ng g⁻¹ and < 1-569 ng g⁻¹, respectively). The distribution of the pesticide residues was very heterogeneous, with the largest concentrations present in one of the studied areas (the province of A Coruña). The distribution of HCH was not found to be related to any soil property (organic matter, pH, clays, and metals). Multivariate statistical analysis of the data revealed that three populations of samples with a defined composition of HCH, can be related to the source of HCH: technical HCH (α/γ > 3), lindane (99% γ-HCH), or both. The existence of a third population consisting almost exclusively of α-HCH suggests that background contamination of anthropogenic origin dates from several decades ago. The detailed analysis of these populations enabled the possible temporal scale of the application of these pesticides to be deduced.     

Atmospheric deposition of persistent organic pollutants to the East Rongbuk Glacier in the Himalayas

To assess levels and seasonal trends of organochlorine pesticides (OCPs) and polychlorinated biphenyls (PCBs) in a high-altitude mountain region, a 2.1 m snowpack sample was collected from the East Rongbuk Glacier at 6572 ma.s.l. on Mt. Everest in September 2005. This snowpack covered a full year period from the fall of 2004 to the summer of 2005 and reflected the major meteorology of the monsoon and non-monsoon seasons. The most abundant compounds detected in the snow samples were γ-hexachlorocyclohexane (γ-HCH) and α-HCH with mean concentrations of 123 pg L^− 1 and 92 pg L^− 1, respectively. This is the first detection of these compounds in recent snow samples from the Himalayas. Backward air trajectory analysis indicated that the Himalayas could be influenced by the major HCH source regions in both India and China. Among the seven marker PCB congeners (PCB 28, 52, 101, 118, 138, 153, and 180) quantified, PCB 28 and PCB 52 were the only dominant PCB congeners detected, with mean concentrations of 17 pg L^− 1 and 6 pg L^− 1, respectively. In addition, DDT metabolites, p,p′-DDE and p,p′-DDD were detected in some snow samples and mean concentrations of DDTs were 24 pg L^− 1. Seasonal differences were observed for α- and γ-HCH concentrations increasing from the non-monsoon season to the monsoon season. Meanwhile, PCB 28 and HCB showed uniform variations with peak concentrations resulting from an effective scavenging by snowfalls between the monsoon and non-monsoon interval. Compared to other high mountain areas, the levels of POPs deposited into the East Rongbuk Glacier were relatively low, resulting from the highest altitude and remoteness from source regions.     

Selected persistent organochlorine pollutants in Romania

Selected persistent organochlorine pollutants, including PCBs, DDT and its metabolites (DDTs) and hexachlorocyclohexane isomers (HCHs) were determined in soil, animal fat and human serum samples from Romania. All methods were rigorously tested and adequate quality control was ensured. Soil samples from Iassy County showed a lower contamination with organochlorines than samples from other Romanian regions. While DDTs concentrations in soil were significantly higher at rural sites, only few samples (three out of 47) exceeded the official Romanian norms for DDTs. PCBs concentrations were low in rural sites (<8 ng/g soil), but rather high (up to 134 ng/g soil) in urban soils collected mostly from parks (Bucharest, Arad, Baia Mare, Pitesti and Ploiesti). Animal fat samples from Iassy showed high concentrations of organochlorine pesticides (HCHs concentrations up to 12370 ng/g fat), but similar PCB concentrations when compared with Arad samples. Two samples (from 24) exceeded the EU norms (1000 ng/g fat) for HCHs and DDTs in animal fat. Organochlorines were found in higher concentrations in some samples of human serum from Timisoara due to a broader age range. Samples of human serum from Iassy mothers showed higher HCHs and DDTs concentrations than samples from a similar group from Antwerp, Belgium. HCB and PCBs were higher in Antwerp cohort. Romanian samples showed a higher ratio DDT/ΣDDTs, but similar ratios PCB 153/ΣPCBs.     

Gradient distribution of persistent organic contaminants along northern slope of central-Himalayas, China

High mountains may serve as condenser for persistent organic pollutants (POPs) and the vegetation in remote areas has been used as a means to characterized atmospheric concentrations of air pollutants. In this study, organochlorine pesticides (OCPs) and polycyclic aromatic hydrocarbons (PAHs) in Himalayan spruce needle samples from Zhangmu-Nyalam region (central-Himalayas) were analyzed and the altitudinal gradient of these pollutants was investigated. Total HCHs and DDTs concentration in needles were in the range of 1.3-2.9 ng g(-1) dry weight and 1.7-11 ng g(-1) dry weight, which were lower than concentrations reported in spruce needles from Alps, however higher than concentrations in conifer needles from mountain areas of Alberta. Total Himalayan spruce needle PAHs was below 600 ng g(-1) and fluorene, phenanthrene and acenaphthene were abundant individual compounds measured. The ratios of alpha-HCH/gamma-HCH in pine needles were similar with the usual values for technical HCH, implying technical HCHs might be used in this region. The high ratios of o-p'-DDT/p-p'-DDT and no p-p'-DDE measured in this study led to the suspicion that a new source of o-p'-DDT and/or p-p'-DDT existed in this region. In addition, higher ratios of low molecular weight-/high molecular weight-PAHs in this region indicated that petroleum combustion, vehicle emission and low-temperature combustion might be the major contributions of PAH source. To examine the POPs distillation, the analyte concentrations were correlated with altitude. The more volatile OCPs, alpha-HCH, gamma-HCH, aldrin and alpha-endosulfan positively correlated with altitude, however, less volatile OCPs (DDT and DDD) inversely related with elevation. Almost all PAHs detected in this area showed positive correlations with altitude. It is worthy to note that heavy PAHs (Benzo[k] fluoranthene and Benzo[a]anthracene) displayed positive correlation, which implied the sources of PAHs were near the sampling sites. The distillation of POPs was strongly affected by the proximity between sampling sites and contaminant sources. If the contaminant sources are close to the mountains, it may be the dominant factor that controls the concentration gradient.     

Hexachlorocyclohexanes (HCH) in ringed seal (Phoca hispida) from Ulukhaktok (Holman), NT: Trends from 1978 to 2006

Trends in α-, β-, and γ-hexachlorocyclohexane (HCH) concentrations were examined in blubber lipid of ringed seals (Phoca hispida) from Ulukhaktok (Holman), NT (Canada) sampled at intervals between 1978 and 2006. α-HCH usually represented approximately 90% of the total HCH isomers. α-HCH and γ-HCH concentrations showed no change over the sampling interval, but β-HCH concentrations increased significantly, about 8-10-fold in females and 4-5-fold in males. Residue concentrations showed no dependence on age. Concentrations (all data as ng/g lipid, GM (range)) of α-HCH were significantly higher (P < 0.001 by t-test) in males (217 (93.9-517), n = 37) than those in females (138 (40.9-402), n = 38). β-HCH concentrations did not differ between the sexes. Concentrations of γ-HCH were significantly higher (P < 0.05) in males (6.74 (0-46.7)) than in females (4.35 (0-19.0)). Although global emissions of both α-HCH and β-HCH have declined since the early 1980's, the “signal” of HCH emission changes has not yet resulted in a “response” in ringed seal residue concentrations. In the light of our current understanding of the dynamics of HCH in the Arctic, we conclude that any such response may not be detected by retrospective analyses of the sort describe here at least for another decade or so, because of the longevity of the seals.     

Occurrence of endocrine disrupting compounds in tissues and body fluids of Belgian dairy cows and its implications for the use of the cow as a model to study endocrine disruption

The reproductive performance of high producing dairy cows has dropped severely throughout the last decades. It has already been suggested that the presence of endocrine disrupting compounds (EDCs) in the environment could be one of the reasons for this declining fertility. Reliable data concerning tissue and body fluid concentrations of these chemicals are thus crucial, but currently only scarcely available. Therefore, we selected dairy cows (≥ 6 years) from diverse locations in Belgium and analysed tissues (liver, adipose tissue, muscle, kidney, and ovaria) and body fluids (serum, follicular fluid, and milk) for their content of potential EDCs, such as polychlorinated biphenyls (PCBs), organochlorine pesticides (OCPs) and polybrominated diphenyl ethers (PBDEs). Furthermore, we collected milk and serum samples from high producing dairy cows 2-3 weeks post-partum to verify if the massive lipolysis required to sustain milk production is accompanied with an increase in EDC concentrations in milk and serum.Overall, contamination was very low (median sum PCBs liver: 11.7 ng g⁻¹ lw), with follicular fluid samples showing no detectable contamination. CB 153 was present in each tissue sample. Strong correlations could be found between EDCs in the same tissue. The increased PCB concentrations observed in milk samples from high producing dairy cows could indicate that massive lipolysis can play a role in liberating and thereby increasing EDC concentrations in milk.Because concentrations of the most prevalent EDCs in dairy cow tissues and body fluids are very low, exposure to EDCs can hardly be considered as a major cause of declining fertility in high producing dairy cows in Belgium. As a result of this low contamination and the similarities between the female bovine and human reproductive physiology, in vitro studies based on Belgian dairy cow ovarian follicles can be considered as a valuable model to study the effects of EDCs on human reproduction.     

Distribution of polychlorinated biphenyls, organochlorine pesticides and polybrominated diphenyl ethers in human umbilical cord serum, maternal serum and milk from Wielkopolska region, Poland

The levels of organochlorinated pesticides (OCPs): p,p'-DDT and its metabolites, hexachlorobenzene (HCB), hexachlorocyclohexane isomers (HCHs), chlordanes and their metabolites, and 18 polychlorinated biphenyl (PCB) congeners were measured in maternal serum, umbilical cord serum and human milk collected from 22 mothers living in the Wielkopolska region, Poland. Additionally, 11 polybrominated diphenyl ether (PBDE) congeners were measured in the human milk samples. p,p'-DDT and its major metabolite, p,p'-DDE, together with HCB, were found in all milk and serum samples. Median concentrations of p,p'-DDE in maternal serum, umbilical cord serum and milk were 343, 329 and 634ng/g lipid weight (lw). PCB congeners 138, 153 and 180 were the major congeners measured in all serum samples, while CB 170 was detected in 74% and 100% of umbilical cord and maternal serum, respectively. Except for CBs 74, 101 and 105, which had a detection frequency of 77%, 23% and 82%, respectively, all investigated PCB congeners were measured in all human milk samples. The median concentrations of sum PCBs in maternal serum, umbilical cord serum and milk were 79, 60 and 133 ng/g lw, respectively. A good correlation (Spearman R(S)>0.75, p<0.001) was found for major PCBs, p,p'-DDT and p,p'-DDE, between maternal and umbilical cord serum, while the correlation was weaker between milk and serum. The median of sum PBDEs in human milk was 2.0 ng/g lw (range 0.8 to 8.4), with BDE 47 being always the most abundant PBDE congener and, together with BDE 153, being present in all samples. In general, results found in the investigated group are at the low end of the concentration range measured in Europe.     

Organochlorine pesticides, polychlorinated biphenyls and trace elements in wild European sea bass (Dicentrarchus labrax) off European estuaries

Polychlorinated biphenyls (PCBs) and organochlorine pesticides like dichloro-diphenyl-trichloroethane (DDTs), hexachlorocyclohexanes (HCHs), aldrin, dieldrin and trace elements (Cd, Cu, Se, Pb, Zn and Hg) were analysed in the muscle of European sea bass (Dicentrarchus labrax) sampled in Atlantic coastal regions near several important European river mouths (Gironde, Charente, Loire, Seine and Scheldt). High contamination levels were measured in the muscles of European sea bass sampled in the coastal regions near those river mouths (e.g. Σ ICES PCB = 133-10,478 μg kg^− 1 lw and Hg = 250-2000 μg kg^− 1 dw).The Scheldt and the Seine are still among the most contaminated estuaries in Europe. Each region presented their specific contamination patterns reflecting different sources due to the input of the respective rivers. As fish and fishery products are the main contributors of the total dietary intake of organochlorinated pollutants, regular consumption of European sea bass with the reported contamination levels may represent a significant exposure route for the general human population.     

The recent deposition of persistent organic pollutants and mercury to the Dasuopu glacier, Mt. Xixiabangma, central Himalayas

High mountains may serve as condensers for persistent organic pollutants (POPs) and the ice/snow core can provide long-term records of atmospheric deposition of pollutants. In this study, organochlorine pesticides (OCPs) and polycyclic aromatic hydrocarbons (PAHs) in firn core from Dasuopu Glacier were analyzed and the seasonal variation and deposition flux of these pollutants were investigated. PCB 28 was always detected in samples from different firn core layers and concentrations of PCB 28 were in the range of 0.09-0.3 ng/l. Hexachlorobenzene (HCB) and total DDTs (p-p'-DDD and p-p'-DDT) were not always detected and were only present in some samples. No p-p'-DDE and hexachlorocyclohexane (HCH) were detected above the level of determination limits. Concentrations of HCB ranged from 0.04 to 0.07 ng/l, and total DDTs were in the range of 0.15-0.3 ng/l. Total glacier PAHs was below 26 ng/l. The levels of OCPs and PAHs in Dasuopu glacier were roughly similar to values from the European mountain areas but lower than those from Lys glacier (Italy) and glacier from Rocky Mountain. Hg concentration (2-35 ng/l) in firn core samples was higher than that of remote region of Arctic. PCB 28 didn't show obvious variation in different seasons, however for major PAH compounds higher values were observed in summer than in winter. With regard to Hg, it displayed winter maximum. Deposition flux of OCPs, PAHs and mercury showed similar results with maximum flux occurring in the 2000s. After 2000/2001, deposition flux decreased and reflected the possible decrease of emissions of these atmospheric pollutants in the adjacent region.     

Contaminant blubber burdens in Atlantic bottlenose dolphins (Tursiops truncatus) from two southeastern US estuarine areas: Concentrations and patterns of PCBs, pesticides, PBDEs, PFCs, and PAHs

Polychlorinated biphenyls (PCBs), chlorinated pesticides (i.e., dichlorodiphenyltrichloroethane (DDT) and its metabolites, chlordanes (CHLs), dieldrin, hexachlorobenzene (HCB), and mirex), polybrominated diphenyl ethers (PBDEs), perfluorinated chemicals (PFCs), and polyaromatic hydrocarbons (PAHs) were measured in blubber biopsy samples collected from 139 wild bottlenose dolphins (Tursiops truncatus) during 2003-2005 in Charleston (CHS), SC and the Indian River Lagoon (IRL), FL. Dolphins accumulated a similar suite of contaminants with ∑ PCB dominating (CHS 64%, IRL 72%), followed by ∑ DDT (CHS 20%, IRL 17%), ∑ CHLs (CHS 7%; IRL 7%), ∑ PBDE (CHS 4%, IRL 2%), PAH at 2%, and dieldrin, PFCs and mirex each 1% or less. Together ∑ PCB and ∑ DDT concentrations contributed ∼ 87% of the total POCs measured in blubber of adult males. ∑ PCBs in adult male dolphins exceed the established PCB threshold of 17 mg/kg by a 5-fold order of magnitude with a 15-fold increase for many animals; 88% of the dolphins exceed this threshold. For male dolphins, CHS (93,980 ng/g lipid) had a higher ∑ PCBs geomean compared to the IRL (79,752 ng/g lipid) although not statistically different. In adult males, the PBDE geometric mean concentration was significantly higher in CHS (5920 ng/g lipid) than the IRL (1487 ng/g). Blubber ∑ PFCs concentrations were significantly higher in CHS dolphins. In addition to differences in concentration of PCB congeners, ∑ PBDE, TEQ, ∑ CHLs, mirex, dieldrin, and the ratios ∑ DDE/∑DDT and trans-nonachlor/cis-nonachlor were the most informative for discriminating contaminant loads in these two dolphin populations. Collectively, the current ∑ PCB, ∑ DDT, and ∑ PBDEs blubber concentrations found in CHS dolphins are among the highest reported values in marine mammals. Both dolphin populations, particularly those in CHS, carry a suite of organic chemicals at or above the level where adverse effects have been reported in wildlife, humans, and laboratory animals warranting further examination of the potential adverse effects of these exposures.     

Organochlorines in Greenland ringed seals (Phoca hispida)

Twenty-five ringed seals (Phoca hispida) were sampled in 1994 at each of four areas in Greenland, three on the west coast and one on the east coast. Seal blubber samples were analysed for polychlorinated biphenyls (PCBs, IUPAC Nos. 28, 31, 52, 101, 105, 118, 138, 153, 156 and 180), DDTs (p,p'-DDE, p,p'-DDD, p,p'-DDT), hexachlorocyclohexanes (alpha-, beta- and gamma-HCH), hexachlorobenzene (HCB) and trans-nonachlor. A number of the seals (n = 56) were also analysed for toxaphene (total toxaphene and single congeners: CHB Nos. 26, 32, 50 and 62). The overall geometric means (and ranges) found in seals were in microgram kg-1 wet wt. for sigma PCBs: 452 (85-4200), sigma DDTs: 607 (97-6040), sigma HCHs: 123 (51-382), HCB: 13 (3-27), trans-nonachlor: 83 (21-1236) and total toxaphene: 263 (71-950). The geometric means for HCB, trans-nonachlor, toxaphenes and the sums of PCBs and DDTs were higher for the east coast samples than for those from the west coast, and a decreasing trend in concentrations followed the east Greenland current. No geographical trend was apparent for HCHs. Differences in concentrations between females and males were only significant for HCB and HCH within certain age classes and sampling areas. A tendency for concentrations to increase with age was observed, but was not statistically significant. Principal component analyses for PCB congeners revealed that the proportion of higher chlorinated PCBs (Cl atoms > or = 6) decreased with decreasing concentrations of PCBs found for the four sampling areas. No differences between the higher and lower chlorinated PCBs were seen in females and males, but a higher proportion of CB-105 and CB-118 compared to CB-52 and CB-101 was seen in male seals compared to female seals.