Chlordane Concentrations Research Articles

Impacts of a warming climate on concentrations of organochlorines in a fasting high arctic marine bird: Direct vs. indirect effects?

The present study examined how climate changes may impact the concentrations of lipophilic organochlorines (OCs) in the blood of fasting High Arctic common eiders (Somateria mollissima) during incubation. Polychlorinated biphenyls (PCBs), 1-dichloro-2,2-bis (p-chlorophenyl) ethylene (p,p′-DDE), hexachlorobenzene (HCB) and four chlordane compounds (oxychlordane, trans-chlordane and trans- and cis-nonachlor) were measured in females at chick hatching (n = 223) over 11 years (2007–2017). Firstly, median HCB and p,p′-DDE concentrations increased ~75 % over the study period, whereas median chlordane concentrations doubled (except for oxychlordane). PCB concentrations, in contrast, remained stable over the study period. Secondly, both body mass and clutch size were negatively associated with OC levels, suggesting that females with high lipid metabolism redistributed more OCs from adipose tissue, and that egg production is an important elimination route for OCs. Thirdly, the direct climate effects were assessed using the mean effective temperature (ET: air temperature and wind speed) during incubation, and we hypothesized that a low ET would increase redistribution of OCs. Contrary to expectation, the ET was positively correlated to most OCs, suggesting that a warmer climate may lead to higher OCs levels, and that the impact of ET may not be direct. Finally, potential indirect impacts were examined using the Arctic Oscillation (AO) in the three preceding winters (AOwinter 1–3) as a proxy for potential long-range transport of OCs, and for local spring climate conditions. In addition, we used chlorophyll a (Chla) as a measure of spring primary production. There were negative associations between AOwinter 1 and HCB, trans-chlordane and trans-nonachlor, whereas oxychlordane and cis-chlordane were negatively associated with Chla. This suggests that potential indirect climate effects on eiders were manifested through the food chain and not through increased long-range transport, although these relationships were relatively weak.

Nationwide assessment of atmospheric organochlorine pesticides over a decade during 2008–2017 in South Korea

Long-term nationwide atmospheric monitoring of organochlorine pesticides (OCPs) was performed in South Korea during 2008–2017. Their occurrences, seasonal and temporal variability, sources, and effect of ambient temperature were investigated. The OCPs are pronounced with a mean concentration of total OCPs ranging from 5.2 to 256 pg/Sm3. However, a decrease of 54 % was observed in the mean concentration of total OCPs from 2008 to 2017 associated with regulatory actions. OCP concentrations did not show any variations between the different site types, and OCPs were ubiquitously present at all site types. The mean concentration of total OCPs in summer was two-fold higher than in winter. The concentrations of DRINs, DDTs, ENDOs, and HCHs were significantly higher in summer, but the concentrations of chlordane and heptachlor were higher in winter. The diagnostic ratios identified major sources as ongoing sources, past use, and atmospheric transport. Clausius Clapeyron plots strongly suggested the re-emission of α-endosulfan, β-endosulfan, α-HCH, and β-HCH, and ΔHsa (enthalpy of surface air exchange) values suggested the influence of the transport and/or new sources on aldrin, dieldrin, and chlordane. The occurrence of OCPs due to re-emissions, ongoing sources, and long-range atmospheric transport could be a challenge towards the complete phase-out of OCPs in South Korea.

On the Organochlorine pesticide residues in the Marshes, Shatt Al-Arab and the Arabian Gulf system

Organochlorine pesticides are a class of toxic compounds characterized by their relative chemical and biological stability. They are ubiquitous in the environments and are soluble in liquids. Consequently Organochlorine pesticides have been placed on “the top of black list” of potential environmental hazards. Studies on Organochlorine residues have been carried out between 1979-1991. The residues were determined in water, sediments and organisms collected from the Marshes, Shatt Al-Arab and the Arabian Gulf system. Most of the data confirmed the present of ∑DDT, Endrin, Dieldrin, Chlordane and Heptachlor. Their concentrations ranged from nd-336, nd-111, 12-195, nd-57 and nd-79 ng/l in dissolved, from 0.1-2560, nd-217, nd-0.97 , nd-171 and nd-679 µg/kg in particulate and from 0.04-220, nd-47, nd-22, nd from nd-24 µg/kg in sediments from 1-189, nd-154, nd-32, nd-58 and nd-6 ppb in fish, from 0.59-784, 166-540, 2-72, 5-3.1 and nd ppb in mussel and from 0.3-6.3, nd-0.4, nd-0.8, nd and nd-0.3 ppb in shrimp respectively. In the last decade only two studies on Organochlorine residues have been done. One of them in the Mesopotamian wetlands of southern Iraq in which residues of p,p´-DDT have been detected in 100% of the examined samples. This indicates its ability to persist under severe drying of previously exposed surface sediments, long period of more than 10 years of previously exposed surface sediments, high temperature, and intensive solar radiation, and the other by using samples of water, sediment, fish and shrimp from Hor Al-Hammar Marshes of Iraq, high concentration of chlordane in both water and sediments were shown. Therefore further work is needed to establish the baseline levels of Organochlorine residue in the Marshes, Shatt Al-Arab and the Arabian Gulf region.

Chlordane exposure causes developmental delay and metabolic disorders in Drosophila melanogaster

The incidence of metabolic diseases is increasing every year, and several studies have highlighted the activity of persistent organic pollutants (POPs) in causing hyperlipidemia and diabetes, and these compounds are considered to be endocrine disrupting chemicals (EDCs). Chlordane is classified as an endocrine disruptor, but the mechanism of how it functions is still unclear. This study investigates the effects of chlordane exposure on Drosophila larvae. Drosophila was cultured in diet containing 0.01 μM, 0.1 μM, 1 μM, 5 μM, and 10 μM chlordane, and the toxicity of chlordane, the growth and development of Drosophila, the homeostasis of glucose and lipid metabolism and insulin signaling pathway, lipid peroxidation-related indicators and Nrf2 signaling pathway were evaluated. We here found that exposure to high concentrations of chlordane decreased the survival rate of Drosophila and that exposure to low concentrations of chlordane caused disruption of glucose and lipid metabolism, increased insulin secretion and impairment of insulin signaling. Notably, it also led to massive ROS production and lipid peroxidation despite of the activation of Nrf2 signaling pathway, an important pathway for maintaining redox homeostasis. Collectively, chlordane causes lipid peroxidation and disrupts redox homeostasis, which may be a potential mechanism leading to impaired insulin signaling and the metabolism of glucose and lipid, ultimately affects Drosophila development.

Occurrence of atmospheric current-use and historic-use pesticides at a CAWNET background site in central China

China as an agricultural country has a considerable amount of pesticide usage. However, studies of current-use pesticides (CUPs) in the background air are very limited. Meanwhile, though historic-use pesticides (HUPs) have been banned globally, the abundance of HUPs in the background areas require urgent attention. In this study, air samples were collected using an active air sampler from January 2018 to January 2019 every six days at a background site (Jinsha, JSH) in central China to investigate the concentrations, seasonal variations and sources of CUPs and HUPs. The total volume for each sampling was 430 m3. Finally, a total of 54 sets of samples was collected. The annual median concentrations (gas plus particle) were 1053 (140–6409) pg m−3 for CUPs and 33.2 (2.12–158) pg m−3 for HUPs, respectively. Pyrethroids were the most abundant class of CUPs, accounting for 97.8% of the total CUPs. Most CUPs exhibited high levels in spring (chlorothalonil and trifluralin) and summer (pyrethroids, chlorpyrifos and dicofol), while no obvious seasonal pattern was observed for HUPs. The results of Clausius-Clapeyron equation and back trajectories suggested that most CUPs (excluding chlorpyrifos) and HUPs (HCHs, chlordane and α-endosulfan) were affected by long-range atmospheric transport, chlorpyrifos and β-endosulfan were influenced by short-range atmospheric transport or re-volatilization, and HCB was affected by regional combustion processes. Moreover, data of HUPs in 2012/2013 from previous studies was used for comparison. From 2012/2013 to 2018/2019, atmospheric concentrations of HCB, chlordane, α-HCH and γ-HCH declined by about 94%, 74%, 85% and 73%, respectively, indicating the effective emission controls of these compounds in China. However, the concentration of α-endosulfan increased by 51%, hinting at the fresh input transported from Anhui, Guangdong and Jiangxi provinces. Therefore, special attention and follow-up control measures should be taken for endosulfan in China.

Impact of environmental exposure to persistent organic pollutants on lung cancer risk

BackgroundRecent studies suggest that high pre-diagnostic serum concentrations of persistent organic pollutants (POPs) might result in the development of cancers in the general population. However, the association between pre-diagnostic serum POP concentrations and lung cancer risk has not been studied. Here, we evaluated associations between low-dose environmental exposure to POPs and risk of lung cancer using pre-diagnostic serum samples in a case-cohort study based on a population-based prospective cohort. MethodsWe conducted a case-cohort study based on the Korean National Cancer Center Community Cohort, from which we included 118 lung cancer cases and 252 controls. Serum concentrations of POPs were measured by high resolution gas chromatography/high-resolution mass spectrometry, and data were analyzed using multivariable Cox proportional-hazards regression models. ResultsRisk of lung cancer increased per unit increase in the natural log-transformed concentrations of the sum of chlordane congeners, total PCBs, and all PCBs subgrouped by the number of chlorines or ortho- substituted chlorines on the molecules, except for tri/tetrachlorobiphenyls, in all models. Among individual POP analytes with a detection rate >80%, after Bonferroni adjustment, only trans-nonachlor was associated with lung cancer risk. In categorical models, risk of lung cancer was associated with serum concentration of chlordane (4th vs. 1st quartile, hazard ratio [95% confidence interval], 8.79 [2.77–27.97]). Dose-dependent relationships were also found between risk of lung cancer and serum concentrations of PCBs regardless of their degree of chlorination, substitution pattern, or binding affinity to receptors (total PCBs, P = 0.002; mid-chlorinated PCBs, P = 0.004; high-chlorinated PCBs, P < 0.001; non- and mono-ortho PCBs, P = 0.031; di-ortho PCBs, P = 0.003; PCBs with dioxin-like activity, P = 0.011; non-dioxin-like non-/mono-ortho PCBs, P = 0.060). ConclusionsSerum concentrations of chlordane and PCBs are associated with risk of lung cancer in the general population, even decades after the ban on their production and use.

Temporal trends of legacy organochlorines in different white-tailed eagle (Haliaeetus albicilla) subpopulations: A retrospective investigation using archived feathers

Understanding the spatiotemporal patterns of legacy organochlorines (OCs) is often difficult because monitoring practices differ among studies, fragmented study periods, and unaccounted confounding by ecological variables. We therefore reconstructed long-term (1939–2015) and large-scale (West Greenland, Norway, and central Sweden) trends of major legacy OCs using white-tailed eagle (Haliaeetus albicilla) body feathers, to understand the exposure dynamics in regions with different contamination sources and concentrations, as well as the effectiveness of legislations. We included dietary proxies (δ13C and δ15N) in temporal trend models to control for potential dietary plasticity. Consistent with the hypothesised high local pollution sources, levels of polychlorinated biphenyls (PCBs), dichlorodiphenyltrichloroethanes (DDTs) and hexachlorocyclohexanes (HCHs) in the Swedish subpopulation exceeded those in the other subpopulations. In contrast, chlordanes (CHLs) and hexachlorobenzene (HCB) showed higher concentrations in Greenland, suggesting the importance of long-range transport. The models showed significantly decreasing trends for all OCs in Sweden in 1968–2011 except for CHLs, which only decreased since the 1980s. Nevertheless, median concentrations of DDTs and PCBs remained elevated in the Swedish subpopulation throughout the 1970s, suggesting that the decreases only commenced after the implementation of regulations during the 1970s. We observed significant trends of increasing concentrations of PCBs, CHLs and HCB in Norway from the 1930s to the 1970s/1980s and decreasing concentrations thereafter. All OC concentrations, except those of PCBs were generally significantly decreasing in the Greenland subpopulation in 1985-2013. All three subpopulations showed generally increasing proportions of the more persistent compounds (CB 153, p.p′-DDE and β-HCH) and decreasing proportions of the less persistent ones (CB 52, p.p′-DDT, α- and γ-HCH). Declining trends of OC concentrations may imply the decreasing influence of legacy OCs in these subpopulations. Finally, our results demonstrate the usefulness of archived museum feathers in retrospective monitoring of spatiotemporal trends of legacy OCs using birds of prey as sentinels.

Polycyclic aromatic hydrocarbons, polychlorinated biphenyls and legacy and current pesticides in indoor environment in Australia – occurrence, sources and exposure risks

Paired indoor air and floor dust samples were collected from residential houses and offices (n = 28) in two Australian cities in 2015. For the air samples, a modified passive air sampler (PAS) was used to collect semi-volatile organic compounds (SVOCs) in gaseous phase and airborne particles simultaneously. Sampling rates (R) of the PAS for gaseous SVOCs ranged from 0.69 to 3.4 m3 sampler−1 day−1. Out of the 33 analytes, 22, 14 and 17 compounds were detected (above the method detection limit) in over 50% of air, airborne particles and floor dust samples respectively. The highest median level in air, airborne particles and floor dust was observed for phenanthrene (2.0 ng m−3), permethrin (8800 ng g−1) and permethrin (5100 ng g−1) respectively. Among polychlorinated biphenyl (PCB) congeners, with few exceptions, the largest contribution was from 3,3′-dichlorobiphenyl (PCB11) for both indoor air and floor dust samples. In these houses and offices, the indoor level of polycyclic aromatic hydrocarbons (PAHs) was mainly influenced by ambient (outdoor) air. Primary sources of PCBs were from within indoor environments and generally older houses have higher concentrations in air. Among pesticides, hexachlorobenzene in indoor environments appeared to be due to transfer from outdoor sources whereas chlordanes and pyrethroids were associated with past and current household application respectively. Compared to data from other countries/regions, concentrations of chlordanes, chlorpyrifos and pyrethroids in indoor air and dust samples from Australia were among the highest whereas PCB and PAH levels were among the lowest. The sum of estimated daily intakes (EDIs) via inhalation and dust contact and ingestion were calculated. The highest median value of EDI was observed for permethrin at 2.8 (for adults) and 74 ng kg−1 day−1 (for toddlers), which are <0.15% of the U.S. EPA reference dose.

Concentrations of organohalogens (PCBs, DDTs, PBDEs) in hunted and stranded Northern sea otters (Enhydra lutris kenyoni) in Alaska from 1992 to 2010: Links to pathology and feeding ecology.

Many organohalogen compounds (OHCs) are persistent organic pollutants (POPs) found in appreciable concentrations in marine predators. While production of some POPs has declined or ceased in recent decades, their capacity for global transport and bioaccumulation results in observations of unchanging or increasing concentrations in marine systems. Sea otters (Enhydra lutris) have been advocated as an environmental sentinel for contaminants due to their longevity, site fidelity and prey species that often overlap with human consumption. Using archived (1992-2010) samples of livers from Northern sea otters (n = 50) from Alaska we examine concentrations of chlordanes (CHLs), polychlorinated biphenyls (PCBs), dichlorodiphenyltrichloroethane (DDTs), and polybrominated diphenyl ethers (PBDEs) and associated metabolites. We found some evidence for declining ΣPCBs over the two decades, however for most animals concentrations were low compared to toxicological thresholds. Six animals had relatively high concentrations of ΣPCBs (mean = 262,000 ng/g lipid weight), ΣDDTs (mean = 8,800 ng/g lw), and ΣPBDEs (mean = 4,600 ng/g lw), with four of these six animals experiencing hepatic parasitism or hepatitis. In order to assess whether differences in POP concentrations are associated with feeding ecology, we examined stable isotopes of C and N in archived muscle and whisker samples. In general, there were no significant relationships between ΣPOP concentrations and stable isotope ratios. There were small differences in stable isotope profiles in animals with high POP concentrations, although it was unclear if these differences were due to feeding ecology or disease processes. This study highlights the importance of considering feeding ecology and necropsy (health and disease status) data while conducting contaminant surveys, and confirms some previous reports of trends in OHCs in Alaska marine mammals.

Concentration and Distribution of Organochlorine Pesticides in Sediments of the Niger River, Nigeria.

Pollution in aquatic ecosystems is a serious environmental concern. There is a great need for constant assessment and monitoring of hazardous substances, particularly in aquatic environments in developing countries, as rivers are media with easy trans-boundary transport of chemical substances. The present study assessed the occurrence and distribution of organochlorine pesticides (OCPs) in the sediments of the Niger River, Nigeria. A total of 120 samples of sediment were collected from 15 locations along the river using Van Veen grab. The Environmental Protection Agency (USEPA) 3570 method with slight modification was used for sample preparation. Organochlorine pesticides were analyzed using Hewlett Packard 5890 series II gas chromatography with electron capture detector. Confirmation of OCPs was performed using a gas chromatograph/mass spectrometer (Shimadzu QP2010) and capillary column type HP1MS (30 m × 0.25 um × 0.25 mm id). The highest concentration of ∑OCPs in the sediment samples of the River Niger (5023±1596 μg/kg, 4672-7009 μg/kg) was detected in a location at Onitsha, while the lowest concentration (1570±204.5, 1214-1820 μg/kg) was detected in a location at the Nicolas River. High values of ∑OCPs (>2000 μg/kg) were detected in all of the locations except in three locations where lower levels were detected. The ∑OCPs were higher during the dry season compared to the rainy season. This may be because the resident time of the sediment transported was higher during the dry season compared to the rainy season, which is characterized by storms, high current, and bottom scour. The chlordane concentration ranged between 24.4 and 134.1 μg/kg dry weight (dw) in locations Nicolas 14 and Lokoja 5; and the Probable Effect Concentration guidelines were exceeded. Dieldrin was detected at very low levels in most of the locations and ranged from 5.67 to 70.3 μg/kg dw in locations Onitsha 9 and 8; and the Probable Effect Concentration guideline was only exceeded in location Onitsha 8; however, the Toxic Effect Concentration guideline was exceeded at all of the locations. Dichlorodiphenyldichloroethane (DDD) was not detected in location Lokoja 6 or 7, and Onitsha 8 and 9, although the concentration in all other locations exceeded the guidelines. Dichlorodiphenyldichloroethylene (DDE) concentrations exceeded the guidelines except in location Nicolas 13. Due to the environmental/human risk and potential danger of the elevated levels of OCPs, there is a need for continuous monitoring of the Niger River. The authors declare no competing financial interests.

Distribution of Organohalogen and Synthetic Musk Compounds in Breast Adipose Tissue of Breast Cancer Patients in Ulster County, New York, USA.

We determined the concentrations of 98 halogenated organic compounds and synthetic musks in breast fat tissues of 50 breast cancer patients (age range: 34-77years) collected during 1996-1998 in Ulster County, New York, USA. Polychlorinated biphenyls (PCBs), organochlorine pesticides (OCPs), polybrominated biphenyl 153 (PBB-153), polybrominated diphenyl ethers (PBDEs), and synthetic musk compounds (SMCs) were analyzed in breast fat tissues, and 46 analytes were found at a detection frequency of ≥ 65% and at concentrations in the decreasing order of OCPs > PCBs > SMCs > PBDEs > PBB-153. PCBs (median: 323ng/g wet wt) and dichlorodiphenyltrichloroethanes (DDTs, median: 293ng/g wet wt) were the major compounds found in breast fat tissues. Among PCB congeners, hexa- and hepta-chlorobiphenyls (60% of total PCBs) were the abundant ones. p,p'-DDE accounted for more than 99% of the total DDT concentrations. The concentrations of SMCs and PBDEs were 1-2 orders of magnitude lower than those of PCBs and DDTs. 1,3,4,6,7,8-Hexahydro-4,6,6,7,8,8-hexamethylcyclopenta-r-2-benzopyran (median: 33ng/g wet wt) was the most abundant SMC, whereas BDE-47 (median: 4.5ng/g wet wt) was the most dominant PBDE congener present in breast tissues. A significant correlation (p < 0.05) between women's age and concentrations of DDTs, chlordanes, hexachlorobenzene and PCBs in breast tissues was found. Concentrations of PCBs, PBDEs, OCPs, and SMCs were not significantly different between malignant and benign tumor cases. This study adds baseline information on target tissue burdens of persistent organic contaminants in breast cancer patients.

Concentrations of POPs based wood preservatives in waste timber from demolished buildings and its recycled products in Japan

One of the major proportions of recycled persistent organic pollutants (POPs)-containing waste is timber originating from old buildings, utility poles, and cross-arms because POPs-based treatments were once a common means of preserving wood. In 2016 and 2017, we conducted the first survey in Japan on the residue concentrations of chlordanes (CHLs), pentachlorophenol (PCP), pentachloroanisole (PCA), and polychloronaphthalenes (PCNs) in waste timber (n = 55) and its recycled products (woodchip, n = 42; particle board, n = 3). In the recycled products, the highest concentrations detected were 0.86 mg kg−1 CHLs, 3.0 mg kg−1 PCP, 1.1 mg kg−1 PCA, and 2.6 mg kg−1 PCNs, which were one to two orders lower than the low POP content (LPC) limits for the environmentally sound management of wastes defined under the Basel Convention (50, 100, and 10 mg kg−1, respectively). In the waste timber, which included bearers and columns from demolished buildings, the highest concentrations were 15 mg kg−1 CHLs, 0.20 mg kg−1 PCP, and 0.036 mg kg−1 PCNs, no higher than about 30% of the LPC limit. The concentration of CHLs in timber bearer was significantly higher than those in timber column (p < 0.05). Although none of the waste timber or recycled products had concentrations exceeding the LPC limits, one means of ensuring low POP concentrations in recycled products is separating timber bearer from timber column when demolishing wooden buildings, according to the results in Japan. The timber column can be used to produce recycled products and the remaining timber can be used for heat utilization and power generation.

Nicotinamide-Modified poly(HEMA-GMA)-Nic Cryogels for Removal of Pesticides

Chlordane is only one of the persistent pesticides used in some countries despite the ban. Removal of chlordane, a severe threat to all living things, was performed using nicotinamide-modified poly (2-hydroxyethyl methacrylate-glycidyl methacrylate), poly(HEMA-GMA)-Nic, polymeric cryogels in this study. Pesticides are practically insoluble in water. For that reason, ethanol is used as a solvent which is not chemically dangerous and easily accessible in every laboratory. As an adsorbent, poly (HEMA-GMA) polymeric cryogels previously synthesized in the literature have been modified using nicotinamide. The modification of poly(HEMA-GMA) with nicotinamide is the first in the literature. Removal of chlordane in alcohol medium has been accomplished exploiting the alcoho-phobic interaction, which was the first indication in our previous study. Structural analysis of poly(HEMA-GMA)-Nic was performed using Fourier transform infrared spectroscopy (FT-IR) and elemental analysis methods. Scanning electron microscopy (SEM) was used to understand the surface morphology of cryogels. Surface area and cavity volume calculations were determined by applying N2 adsorption method and swelling test. The interaction time and maximum adsorption capacity were identified as 5 minutes and 64.61 mg chlordane/g cryogel for 300 mg/L chlordane concentration and 108.818 mg chlordane/g cryogel for 800 mg/L chlordane concentration during the adsorption experiments. Cyclohexane, toluene, chloroform, dichloromethane, acetone, and acetonitrile were used as solvent to observe the solvent effect on adsorption of chlordane onto the polymeric material. As expected, the removal of chlordane was performed with the highest adsorption performance in cyclohexane with the lowest dielectric constant.

EROD activity, chromosomal damage, and oxidative stress in response to contaminants exposure in tree swallow (Tachycineta bicolor) nestlings from Great Lakes Areas of Concern.

Tree swallow, Tachycineta bicolor, nestlings were collected from 60 sites in the Great Lakes, which included multiple sites within 27 Areas of Concern (AOCs) and six sites not listed as AOCs from 2010 to 2014. Nestlings, approximately 12 days-of-age, were evaluated for ethoxyresorufin-O-dealkylase (EROD) activity, chromosomal damage, and six measures of oxidative stress. Data on each of these biomarkers were divided into four equal numbered groups from the highest to lowest values and the groups were compared to contaminant concentrations using multivariate analysis. Contaminant concentrations, from the same nestlings, included polychlorinated biphenyls (PCBs), polybrominated diphenyl ethers (PBDEs), perfluorinated compounds (PFCs), and 17 elements. Alkylated polycyclic aromatic hydrocarbons (aPAHs) and parent PAHs (pPAHs) were measured in pooled nestling dietary samples. Polychlorinated dibenzo-p-dioxins, polychlorinated dibenzofurans, and pesticides were measured in sibling eggs. Concentrations of aPAHs, pPAHs, chlordane, dieldrin, heptachlor, and PCBs, in that order, were the major contributors to the significant differences between the lowest and highest EROD activities; PFCs, PBDEs, the remaining pesticides, and all elements were of secondary importance. The four categories of chromosomal damage did not separate out well based on the contaminants measured. Concentrations of aPAHs, pPAHs, heptachlor, PCBs, chlordane, and dieldrin were the major contributors to the significant differences between the lowest and highest activities of two oxidative stress measures, total sulfhydryl (TSH) activity and protein bound sulfhydryl (PBSH) activity. The four categories of thiobarbituric acid reacting substances (TBARS), oxidized glutathione (GSSG), reduced glutathione (GSH), and the ratio of GSSG/GSH did not separate well based on the contaminants measured.

Environmental and behavioral changes may influence the exposure of an Arctic apex predator to pathogens and contaminants

Recent decline of sea ice habitat has coincided with increased use of land by polar bears (Ursus maritimus) from the southern Beaufort Sea (SB), which may alter the risks of exposure to pathogens and contaminants. We assayed blood samples from SB polar bears to assess prior exposure to the pathogens Brucella spp., Toxoplasma gondii, Coxiella burnetii, Francisella tularensis, and Neospora caninum, estimate concentrations of persistent organic pollutants (POPs), and evaluate risk factors associated with exposure to pathogens and POPs. We found that seroprevalence of Brucella spp. and T. gondii antibodies likely increased through time, and provide the first evidence of exposure of polar bears to C. burnetii, N. caninum, and F. tularensis. Additionally, the odds of exposure to T. gondii were greater for bears that used land than for bears that remained on the sea ice during summer and fall, while mean concentrations of the POP chlordane (ΣCHL) were lower for land-based bears. Changes in polar bear behavior brought about by climate-induced modifications to the Arctic marine ecosystem may increase exposure risk to certain pathogens and alter contaminant exposure pathways.

Correlation between toxic organochlorine pesticides and breast cancer.

Organochlorines (OCs) are common environmental pollutants that have been linked to cancer. This work aims to assess the role of OCs as a risk factor for breast cancer and to evaluate the cellular changes induced by exposure to such environmental contaminants. The study included 70 cancer patients subjected to thorough history taking and routine investigations. Samples from tumor and normal adjacent tissue were taken to measure OCs' levels and to perform molecular analysis (some oncogenic and apoptotic markers) by flow cytometry. There were significantly higher concentrations of methoxychlor, dichloro-diphenyl-trichloroethane (DDT), hexa-chlorobenzene (HCB), and chlordane in tumor tissue samples compared to the surrounding normal tissue. There was a positive statistically significant correlation between G2m and dichloro-diphenyl-dichloroethane, DDT, and methoxychlor. There was also a negative correlation between propidium iodide (PI) and heptachlor as well as between PI, B-cell lymphoma 2, and methoxychlor. Annexin showed a negative correlation with HCB and methoxychlor. In conclusion, the higher level of organochlorine pesticides in the tissue specimens of breast cancer and the resultant molecular dysfunction highlight a possible association. Further research is warranted to elucidate the other possible mechanisms involved in the process of carcinogenesis.

Distribution and enantiomeric profiles of organochlorine pesticides in surface sediments from the Bering Sea, Chukchi Sea and adjacent Arctic areas

The spatial distribution, compositional profiles, and enantiomer fractions (EFs) of organochlorine pesticides (OCPs), including hexachlorocyclohexanes (HCHs), dichlorodiphenyltrichloroethanes (DDTs), and chlordanes (CHLs), in the surface sediments in the Bering Sea, Chukchi Sea and adjacent areas were investigated. The total concentrations of DDTs, HCHs and CHLs varied from 0.64 to 3.17 ng/g dw, 0.19–0.65 ng/g dw, and 0.03–0.16 ng/g dw, respectively. No significant difference was observed between the Bering Sea and Chukchi Sea for most pollutants except for trans-CHL, ΣCHLs (sum of trans- and cis-chlordane) and p,p'-DDD. Concentration ratios (e.g., α-HCH/γ-HCH, o,p'-DDT/p,p'-DDT) indicated that the contamination in the studied areas may result from inputs from multiple sources (e.g., historical usage of technical HCHs as well as new input of dicofol). Chiral analysis showed great variation in the enantioselective degradation of OCPs, resulting in excess of (+)-enantiomer for α-HCH in thirty of the 32 detectable samples, preferential depletion of (−)-enantiomer for o,p'-DDT in nineteen of the 35 detectable samples, and nonracemic in most samples for trans- and cis-chlordane. The ecological risks of the individual OCPs as well as the mixture were assessed based on the calculation of toxic units (TUs), and the results showed the predominance of DDT and γ-HCH in the mixture toxicity of the sediment. Overall, the TUs of OCPs in sediments from both the Bering and Chukchi Seas are less than one, indicating low ecological risk potential.

The long shadow of our chemical past – High DDT concentrations in fish near a former agrochemicals factory in England

A total of 81 roach (Rutilus rutilus) collected from 13 southern English river sites between 2007 and 2012, were analysed for organochlorine pesticides, PCBs, PBDEs and some metals. Unexpectedly high concentrations of the banned insecticide DDT and its degradation products DDE and DDD (∑DDTs) were found in the 10 fish from the river Lee (or Lea) which averaged 88 ± 70 (standard deviation) μg/kg ww, almost 20 times higher than the average for the remaining sites (4.8 ± 3.1 μg/kg). All fish from that site exceeded the Canadian Tissue Residue Guideline (environmental quality standard) of 14 μg/kg ∑DDTs. Concentrations of the insecticides chlordane and lindane as well as copper, which is often used as a fungicide, were also elevated in fish from the Lee, though not as much as those of DDTs. A likely explanation for these observations was found in a nearby former pesticide factory, which had stopped production about three decades earlier.An extensive review of recent literature data on DDT in wild European fish found that, while levels are now generally low, there were several other hotspots with ∑DDTs levels that may still be of concern.

Organochlorine Pesticides (OCPs) in Sediment and Fish of Two Tropical Water Bodies Under Different Land Use.

In this study we quantified and compared bioaccumulated OCPs in target fish species Cichlasoma urophthalmus (Mayan cichlid) and Oreochromis niloticus (Nile tilapia) and sediment in two lentic systems neighboring areas with different land use (Xnoha=agricultural/Mocu=nature reserve). Fish at both sites showed the same number of pesticide compounds (17) while in sediment were 17 and 20, respectively. ∑chlordane concentrations were significantly higher in Xnoha in both fish and sediment (1.0 and 0.17µg/g, respectively). Here higher concentrations of o,p'DDT were found in fish than in sediments, this was similarly demonstrated in Mocu but to a lesser extent. The proportion of endosulfan sulfate was lower in Xnoha (<20%) than in Mocu (<50%) compared to the original product. Detected concentrations of ∑DDT and chlordane exceed international permissible limits. Results indicate that OCPs were present in both aquatic systems regardless of the differences in land use.

Measuring and Modeling Organochlorine Pesticide Response to Activated Carbon Amendment in Tidal Sediment Mesocosms.

Activated carbon (AC) sediment amendment for hydrophobic organic contaminants (HOCs) is attracting increasing regulatory and industrial interest. However, mechanistic and well-vetted models are needed. Here, we conduct an 18 month field mesocosm trial at a site containing dichlorodiphenyltrichloroethane (DDT) and chlordane. Different AC applications were applied and, for the first time, a recently published mass transfer model was field tested under varying experimental conditions. AC treatment was effective in reducing DDT and chlordane concentration in polyethylene (PE) samplers, and contaminant extractability by Arenicola brasiliensis digestive fluids. A substantial AC particle size effect was observed. For example, chlordane concentration in PE was reduced by 93% 6 months post-treatment in the powdered AC (PAC) mesocosm, compared with 71% in the granular AC (GAC) mesocosm. Extractability of sediment-associated DDT and chlordane by A. brasiliensis digestive fluids was reduced by at least a factor of 10 in all AC treatments. The model reproduced the relative effects of varying experimental conditions (particle size, dose, mixing time) on concentrations in polyethylene passive samplers well, in most cases within 25% of experimental observations. Although uncertainties such as the effect of long-term AC fouling by organic matter remain, the study findings support the use of the model to assess long-term implications of AC amendment.