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Sample records for dichlorodiphenyl dichloroethylene

  1. Polychlorinated biphenyl (PCB) and dichlorodiphenyl dichloroethylene (DDE) concentrations in the breast milk of women in Quebec.

    PubMed Central

    Dewailly, E; Ayotte, P; Laliberté, C; Weber, J P; Gingras, S; Nantel, A J

    1996-01-01

    OBJECTIVES: This study documented the concentration of polychlorinated biphenyls (PCBs) and dichlorodiphenyl dichloroethylene (DDE) in the breast milk of women from Quebec, Canada, and assessed the impact of various sociodemographic and lifestyle factors on these levels. METHODS: From 1988 to 1990, milk samples were obtained from 536 Quebec women and analyzed for seven PCB congeners and p,p'-DDE. Information was obtained on subjects' physical, sociodemographic, and lifestyle characteristics. RESULTS: Mean concentrations were 0.52 mg/kg lipids (95% confidence interval [CI] = 0.50, 0.54) and 0.34 mg/kg lipids (95% CI = 0.32, 0.35) for PCBs (Aroclor 1260) and DDE, respectively. Age and history of breast-feeding showed statistically significant correlations with PCB and DDE concentrations. CONCLUSIONS: Concentrations of PCBs and DDE measured in this study are at the lower end of the concentration range recently reported for women living in industrialized countries. The modulating factors identified here should be considered when conducting studies on organochlorine exposure and disease. PMID:8806375

  2. p,p\\'-Dichlorodiphenyl dichloroethane (DDD)

    Integrated Risk Information System (IRIS)

    p , p ' - Dichlorodiphenyl dichloroethane ( DDD ) ; CASRN 72 - 54 - 8 Human health assessment information on a chemical substance is included in the IRIS database only after a comprehensive review of toxicity data , as outlined in the IRIS assessment development process . Sections I ( Health Hazard

  3. trans-1,2-Dichloroethylene

    Integrated Risk Information System (IRIS)

    trans - 1,2 - Dichloroethylene ; CASRN 156 - 60 - 5 Human health assessment information on a chemical substance is included in the IRIS database only after a comprehensive review of toxicity data , as outlined in the IRIS assessment development process . Sections I ( Health Hazard Assessments for No

  4. cis-1,2-Dichloroethylene

    Integrated Risk Information System (IRIS)

    cis - 1,2 - Dichloroethylene ; CASRN 156 - 59 - 2 Human health assessment information on a chemical substance is included in the IRIS database only after a comprehensive review of toxicity data , as outlined in the IRIS assessment development process . Sections I ( Health Hazard Assessments for Nonc

  5. IRIS Toxicological Review of cis- & trans-1,2-Dichloroethylene (2010 Final)

    EPA Science Inventory

    The final Toxicological Review of cis- & trans-1,2-Dichloroethylene provides scientific support and rationale for the hazard and dose-response assessment pertaining to chronic exposure to cis- and trans-1,2-dichloroethylene. 1,2-Dichloroethylene is used as a solvent for wa...

  6. 1,1-Dichloroethylene (1,1-DCE)

    Integrated Risk Information System (IRIS)

    1,1 - Dichloroethylene ( 1,1 - DCE ) ; CASRN 75 - 35 - 4 Human health assessment information on a chemical substance is included in the IRIS database only after a comprehensive review of toxicity data , as outlined in the IRIS assessment development process . Sections I ( Health Hazard Assessments f

  7. TOXICOLOGY OF TRANS-1,2-DICHLOROETHYLENE IN THE MOUSE

    EPA Science Inventory

    Trans-1,2-dichloroethylene (DCE) was administered to male and female CD-1 mice in order to evaluate its effects on standard toxicological parameters. Following an acute LD50 determination (2122 mg/kg in males and 2391 mg/kg in females) and a 14-day range-finding study, a 90-day d...

  8. IRIS Toxicological Review of cis- & trans-1,2-Dichloroethylene (Interagency Science Discussion Draft)

    EPA Science Inventory

    EPA is releasing the draft report, Toxicological Review of cis-1,2-Dichloroethylene and trans-1,2-Dichloroethylene, that was distributed to Federal agencies and White House Offices for comment during the Science Discussion step of the Polychlorinated biphenyls (PCBs) and dichlorodiphenyl dichloroethene (DDE) in human milk: effects on growth, morbidity, and duration of lactation

    SciTech Connect

    Rogan, W.J.; Gladen, B.C.; McKinney, J.D.; Carreras, N.; Hardy, P.; Thullen, J.; Tingelstad, J.; Tully, M.

    1987-10-01

    The authors followed 858 children from birth to one year of age to determine whether the presence of polychlorinated biphenyls (PCBs) and dichlorodiphenyl dichloroethene (DDE) in breast milk affected their growth or health. Neither chemical showed an adverse effect on weight or frequency of physician visits for various illnesses, although differences were seen between breast-fed and bottle-fed children, with bottle-fed children being heavier and having more frequent gastroenteritis and otitis media. Children of mothers with higher levels of DDE were breast-fed for markedly shorter times, but adjustments for possible confounders and biases did not change the findings. In absence of any apparent effect on the health of the children, they speculate that DDE may be interfering with the mother's ability to lactate, possibly because of its estrogenic properties.

  9. IRIS Toxicological Review of Cis-& Trans-1,2-Dichloroethylene (External Review Draft)

    EPA Science Inventory

    EPA is conducting a peer review of the scientific basis supporting the human health hazard and dose-response assessment of cis- and trans-1,2-dichloroethylene that will appear in the Integrated Risk Information System (IRIS) database.

  10. Polychlorinated biphenyls (PCBs) and dichlorodiphenyl dichloroethene (DDE) in human milk: effects of maternal factors and previous lactation

    SciTech Connect

    Rogan, W.J.; Gladen, B.C.; McKinney, J.D.; Carreras, N.; Hardy, P.; Thullen, J.; Tingelstad, J.; Tully, M.

    1986-03-01

    The authors measured polychlorinated biphenyls (PCBs) and dichlorodiphenyl dichloroethene (DDE) in maternal serum, cord blood, placenta, and serial samples of breast milk from 868 women. Almost all samples of breast milk showed detectable levels of both chemicals. Overall, values for DDE in this study are within the range of those found previously, whereas those for PCBs are somewhat higher. Possible causes of variation in levels were investigated. For DDE, older women, Black women, cigarette smokers, and women who consumed sport fish during pregnancy had higher levels; only age and race showed large effects. For PCBs, older women, women who regularly drink alcohol, and primiparae had higher levels. In addition, both chemicals showed modest variation across occupational groupings. Casual exposure to a PCB spill did not result in chemical levels different from background. In general, women have higher levels in their first lactation and in the earlier samples of a given lactation, and levels decline both with time spend breast-feeding and with number of children nursed. These striking declines are presumably a measured of exposure to the child.

  11. IRIS Toxicological Review of cis- & trans-1,2-Dichloroethylene (Interagency Science Consultation Draft)

    EPA Science Inventory

    On September 24, 2009, the Toxicological Review of cis- and trans-1,2-dichloroethylene and the charge to external peer reviewers were released for external peer review and public comment. The Toxicological Review and charge were reviewed internally by EPA and by other federal ag...

  12. Selenylation of cis- and trans-1,2-dichloroethylenes and vinylidene chloride under the conditions of phase-transfer catalysis

    SciTech Connect

    Martynov, A.V.; Mirskova, A.N.; Voronkov, M.G.

    1987-06-10

    The reaction of PhSeH with cis- and trans-CHCl=CHCl, catalyzed by tributylbenzylammonium chloride, in 36% sodium hydroxide solution with and without the presence of diethyl ether gives cis-PhSeCH=CHCl. The reaction also leads to the formation of trans-PhSeCH=CHCl and PhSeCCl=CH/sub 2/ in small amounts, depending on the type of dichloroethylene and the presence of diethyl ether. Phenyl benzyl selenide is a side product for all the dichloroethylene isomers. The formation of the isomeric selenides was explained by the trans- and cis-addition of the selenol to the in situ generated chloroacetylene.

  13. Inhibition of mixed function oxidases in rat liver by trans- and cis-1,2-dichloroethylene.

    PubMed

    Freundt, K J; Macholz, J

    1978-06-01

    A single 8-h exposure to trans-1,2-dichloroethylene (t-DCE) or cis-1,2-dichloroethylene (c-DCE) at 200 ppm (hygienic standard in workplaces) resulted in a significant increase in the hexobarbital sleeping time, the zoxazolamine paralysis time, and the metabolic formation of 4-aminoantipyrine from aminopyrine in adult female Wistar rats. Higher DCE concentrations caused a dose-dependent and substantial enhancement of these effects, the effects of c-DCE being stronger than that of t-DCE. In the course of enzyme-kinetic measurements in isolated rat liver microsomes, t-DCE proved to be a competitive inhibitor of the oxidative N-demethylation of aminopyrine and of the O-demethylation of p-nitroanisole. It is concluded from the results that the inhibition of hepatic drug metabolism is caused by a competitive and reversible interaction of the 2 DCE isomers with the mixed-function oxidase system, the interaction possibly operating at the type I binding site. PMID:684758

  14. BIOTRANSFORMATION OF CIS-1,2-DICHLOROETHYLENE IN AQUIFER MATERIAL FROM PICATINNY ARSENAL, MORRIS COUNTY, NEW JERSEY

    EPA Science Inventory

    Soil cores were collected within and adjacent to a trichloroethylene plume that had contaminated the shallow aquifer at Picatinny Arsenal, New Jersey, to study the rate of contaminated cis-1,2-dichloroethylene biotransformation. oil cores also were collected at a highly contamina...

  15. Biotransformation of cis-1,2-dichloroethylene in aquifer material from Picatinny Arsenal, Morris County, New Jersey. Water Resources Investigation

    SciTech Connect

    Ehlke, T.A.; Imbrigiotta, T.E.; Wilson, B.H.; Wilson, J.T.

    1991-01-01

    Soil cores were collected within and adjacent to a trichloroethylen plume that has contaminated the shallow aquifer at Picatinny Arsenal, New Jersey, to study the rate of cis-1,2-dichloroethylene biotransformation. Soil cores also were collected at a highly contaminated site within the plume to determine the effect of different electron donors on the rate of cis-1,2-dichloroetylene biotransformation under methanogenic conditions. Ground-water samples were analyzed for volatile organic compounds to study the relation between volatile-organic-compound concentrations and the biotransformation of cis-1,2-dichloroethylene. Biotransformation in microcosms from sites within the plume ranged from slight to more than 90 percent after an incubation period of 32 weeks. The most extensive biotransformation in soil microcosms occurred at a site near the highest in situ cis-1,2-dichloroethylene concentration measured at the arsenal (710 micrograms per liter). Biotransformation was negligible at an uncontaminated site. Amendment of soil microcosms with combinations of methanol, formate, toluene, p-cresol, propionate, and butyrate inhibited the biotransformation of cis-1,2-dichloroethylene. A combination of methanol and formate had the greatest inhibitory effect.

  16. Applications of Group Theory: Infrared and Raman Spectra of the Isomers of 1,2-Dichloroethylene: A Physical Experiment

    ERIC Educational Resources Information Center

    Craig, Norman C.; Lacuesta, Nanette N.

    2004-01-01

    A study of the vibrational spectroscopy of the cis and trans isomers of 1,2-dichloroethylene provides an excellent opportunity to learn the applications group theory in laboratories. The necessity of using infrared (IR) spectroscopy and Raman spectroscopy in making full vibrational assignments is illustrated.

  17. LACK OF ANTIANDROGENIC EFFECTS IN ADULT MALE RATS FOLLOWING ACUTE EXPOSURE TO 2, 2-BIS (4-CHLOROPHENYL)-1,1-DICHLOROETHYLENE (P,P'DDE)

    EPA Science Inventory

    Although the insecticide dichlorodiphenyltrichloroethane (DDT) was banned in the US in 1972, DDT and its major metabolite 2,2-bis(4-chlorophenyl)-1,1-dichloroethylene (DDE) are still persistent in the environment. DDE at high doses is antiandrogenic in fetal and adult rats and, t...

  18. Remote monitoring of sub ppb levels of vinyl chloride, dichloroethylene and trichloroethylene via modem operated automated GC

    SciTech Connect

    Linenberg, A.; Lander, N.J.

    1994-12-31

    The need for remote monitoring of certain compounds in a sparsely populated area with limited user assistance led to the development and manufacture of a self contained, portable gas chromatography with the appropriate software. Part per billion levels of vinyl chloride, cis 1,2 dichloroethylene and trichloroethylene were detected in air using a trap for preconcentration of the compounds. The units were continuously calibrated with certified standards from Scott Specialty Gases, which in one case was 1 part per billion of the aforementioned compounds. The entire operation of the units, including monitoring instrument responses, changing operating parameters, data transfer, data review and data reporting was done entirely on a remote basis from approximately 600 miles away using a remote computer with a modem and remote operating software. The entire system concept promises the availability of highly sensitive remote monitoring in sparsely populated areas for long periods of time.

  19. Oxidation of trichloroethylene, 1,1-dichloroethylene, and chloroform by toluene/o-xylene monooxygenase from Pseudomonas stutzeri OX1

    SciTech Connect

    Chauhan, S.; Wood, T.K.; Barbieri, P.

    1998-08-01

    Toluene/o-xylene monooxygenase (ToMO) from Pseudomonas stutzeri OX1, which oxidizes toluene and o-xylene, was examined for its ability to degrade the environmental pollutants trichloroethylene (TCE), 1,1-dichloroethylene (1,1-DCE), cis-1,2-DCE, trans-1,2-DCE, chloroform, dichloromethane, phenol, 2,4-dichlorophenol, 2,4,5-trichlorophenol, 2,4,6-trichlorophenol, 2,3,5,6-tetrachlorophenol, and 2,3,4,5,6-pentachlorophenol. Escherichia coli JM109 that expressed ToMO from genes on plasmid pBZ1260 under control of the lac promoter degraded TCE, 1,1-DCE, and chloroform at initial rates of 3.1, 3.6, and 1.6 nmol, respectively. Stoichiometric amounts of chloride release were seen, indicating mineralization. Thus, the substrate range of ToMO is extended to include aliphatic chlorinated compounds.

  1. Stable carbon isotope fractionation of trans-1,2-dichloroethylene during co-metabolic degradation by methanotrophic bacteria

    USGS Publications Warehouse

    Brungard, K.L.; Munakata-Marr, J.; Johnson, C.A.; Mandernack, K.W.

    2003-01-01

    Changes in the carbon isotope ratio (??13C) of trans-1,2-dichloroethylene (t-DCE) were measured during its co-metabolic degradation by Methylomonas methanica, a type I methanotroph, and Methylosinus trichosporium OB3b, a type II methanotroph. In closed-vessel incubation experiments with each bacterium, the residual t-DCE became progressively enriched in 13C, indicating isotopic fractionation. From these experiments, the biological fractionation during t-DCE co-metabolism, expressed as ??, was measured to be -3.5??? for the type I culture and -6.7??? for the type II culture. This fractionation effect and subsequent enrichment in the ??13C of the residual t-DCE can thus be applied to determine the extent of biodegradation of DCE by these organisms. Based on these results, isotopic fractionation clearly warrants further study, as measured changes in the ??13C values of chlorinated solvents could ultimately be used to monitor the extent of biodegradation in laboratory or field settings where co-metabolism by methanotrophs occurs. ?? 2002 Elsevier Science B.V. All rights reserved.

  2. In situ bioremediation of a cis-dichloroethylene-contaminated aquifer utilizing methane-rich groundwater from an uncontaminated aquifer.

    PubMed

    Takeuchi, Mio; Nanba, Kenji; Iwamoto, Hiroshi; Nirei, Hisashi; Kusuda, Takashi; Kazaoka, Osamu; Owaki, Masato; Furuya, Ken

    2005-06-01

    At a trichloroethylene (TCE)-contaminated site in Chikura, Chiba, Japan, TCE had spread over to the first and second aquifers over years. After 8 years of pumping and treatment, finally derivative of TCE, cis-dichloroethylene (c-DCE) remained only in the second aquifer. In this study, feasibility of a low cost in situ bioremediation utilizing groundwater of the third aquifer, which contained natural dissolved methane possibly derived from natural gas field nearby, to stimulate methane-oxidizing bacteria was examined. In vitro experiment showed that a mixture of the groundwater from the second and third aquifers stimulated a growth of methane oxidizing bacteria and enhanced c-DCE degradation. The groundwater of the third aquifer was introduced into the second aquifer in situ. The population of methanotrophs with high V(max) and K(m) for methane uptake increased, resulting in successful degradation of c-DCE at a monitoring well 2m downgradient of the injection well. PMID:15955544

  3. Applications of Group Theory: Infrared and Raman Spectra of the Isomers of cis- and trans-1,2-DICHLOROETHYLENE

    NASA Astrophysics Data System (ADS)

    Craig, Norman C.

    2015-06-01

    A study of the vibrational spectra of cis- and trans-1,2-dichloroethylene provides an excellent way for undergraduates to gain experience with the application of group theory in the physical chemistry laboratory. Although the group vibrations are similar for these two molecules, the selection rules for infrared (IR) and Raman spectra differ significantly. Most of the transitions for the fundamentals of the cis isomer of C2v symmetry are both IR and Raman active. Mutual exclusion for the vibrational transitions applies to the centrosymmetric trans isomer of C2h symmetry. Thus, half the transitions for the trans isomer are IR active and half are Raman active. The two isomers are volatile enough that gas-phase IR spectra can be recorded at room temperature. Band shapes in gas-phase IR spectra provide additional evidence for assignments of fundamentals. The two isomers are small enough that good quality quantum chemical calculations of harmonic frequencies can be done by students with commercial software.

  4. Histochemical and immunocytochemical evidence of early, selective bile canaliculi injury after 1,1-dichloroethylene in rats.

    PubMed Central

    Moslen, M. T.; Dunsford, H. A.; Karnasuta, C.; Chieco, P.; Kanz, M. F.

    1989-01-01

    Canalicular and mitochondrial membranes were investigated as early foci of hepatocyte injury in fed and fasted male Sprague-Dawley rats given 50 mg of 1,1-dichloroethylene (DCE)/kg. Staining of the bile canaliculi localized enzymes, leucine aminopeptidase (LAP), and Mg++-dependent ATPase (Mg++-ATPase), was examined by histochemistry in frozen sections. Mitochondrial membrane enzymes, including succinate dehydrogenase, also were examined by histochemistry. Staining of two monoclonal antibodies, C-1 and 9-B1, whose binding is localized in the bile canalicular region, was examined by immunofluorescence in frozen sections. Fasted rats treated with DCE developed moderate liver damage by 4 hours as evidenced by increases in serum transaminase and bilirubin, whereas fed rats developed only slight cell damage. Centrolobular loss of immunocytochemical and histochemical canalicular staining, especially for C-1 and Mg++-ATPase, was evident as early as 1 hour after DCE and was striking by 2 hours in both fed and fasted rats. Decreases in mitochondrial enzymes were not evident histochemically in fed animals at any time after DCE and were found only at the later times in fasted animals given the toxin. Thus, DCE administration to fed rats provides a new model system of selective bile canaliculi injury. Images Figure 5 Figure 6 Figure 7 Figure 8 PMID:2541611

  5. Modeling the difference among Cucurbita in uptake and translocation of p,p'-dichlorophenyl-1,1-dichloroethylene.

    PubMed

    Gent, Martin P N; White, Jason C; Eitzer, Brian D; Mattina, MaryJane Incorvia

    2007-12-01

    Uptake of organic chemicals into plants depends on the properties of the contaminant and the physiology of the plant. A mass balance model based on fugacity was developed to quantify the uptake and transport in plants of a very hydrophobic chemical, p,p'-dichlorophenyl-1,1-dichloroethylene (DDE). The model included processes for sorption or influx of chemical with water from hydroponic solution to root and sorption or exchange of chemical between the shoot and air. Movement among compartments of the plant was governed by the transfer of water in xylem and phloem. The movement of water was entirely determined by transpiration, growth rate, and weight distribution among tissues. This model was used to predict the kinetics of uptake and movement of DDE from hydroponic solution by seedlings of two species of Cucurbitacea, cucumber and zucchini. These predictions were compared to the results of experiments in a companion paper. These experiments showed that the translocation of DDE in zucchini was much greater than in cucumber. The model correctly predicted the negligible uptake into the shoot of cucumber. The model predicted the greater uptake of DDE by zucchini only if the apparent partitioning of DDE in the xylem was 25-fold higher than that expected in pure water. Predictions using similar parameters were made for uptake and distribution of DDE for plants grown into fruit production in field soil contaminated with DDE. To match the observed concentration of DDE in fruit, the model coefficient for partitioning of DDE into water in phloem had to be increased to 200 times that in pure water. PMID:18020672

  6. NTP Technical Report on the toxicity studies of trans-1,2-dichloroethylene (CAS no. 156-60-5) administered in microcapsules in feed to F344/N rats and B6C3F(1) mice.

    PubMed

    Ress, Nancy B

    2002-04-01

    1,2-Dichloroethylene exists in two isomeric states: trans-1,2-dichloroethylene and cis-1,2-dichloroethylene. The trans isomer is used more widely in industry than the cis isomer. trans-1,2-Dichloroethylene is used as a solvent for waxes, resins, and acetylcellulose. It is also used in the extraction of rubber, as a refrigerant, and in the manufacture of pharmaceuticals and artificial pearls. F344/N rats and B6C3F1 mice were administered trans-1,2-dichloroethylene in microcapsules in feed for 14 weeks. Animals were evaluated for clinical pathology, reproductive system effects, and histopathology. Genetic toxicity studies were conducted in vitro in Salmonella typhimurium and Chinese hamster ovary (CHO) cells, and in vivo in mouse bone marrow cells and peripheral blood erythrocytes. In the 14-week feed studies, groups of 10 male and 10 female rats and mice were fed diets containing microcapsules with a chemical load of 45% trans-1,2-dichloroethylene. Dietary concentrations of 3,125, 6,250, 12,500, 25,000, and 50,000 ppm microencapsulated trans-1,2-dichloroethylene resulted in average daily doses of 190, 380, 770, 1,540, and 3,210 mg/kg for male rats; 190, 395, 780, 1,580, and 3,245 mg/kg for female rats; 480, 920, 1,900, 3,850, and 8,065 mg/kg for male mice; and 450, 915, 1,830, 3,760, and 7,925 mg/kg for female mice. Additional groups of 10 male and 10 female rats and mice served as untreated and vehicle controls. There were no exposure-related deaths of rats or mice. Mean body weights of male rats and male and female mice in the 50,000 ppm groups were significantly less than those of the vehicle controls. The mean body weight gains of female mice in the 12,500 and 25,000 ppm groups were also significantly less than that of the vehicle controls. On day 21 and at week 14, there were mild decreases in hematocrit values, hemoglobin concentrations, and erythrocyte counts in groups of male and female rats in the 25,000 and 50,000 ppm groups. At week 14, these effects were

  7. pH impact on reductive dechlorination of cis-dichloroethylene by Fe precipitates: an X-ray absorption spectroscopy study.

    PubMed

    Jeong, Hoon Y; Anantharaman, Karthik; Hyun, Sung P; Son, Moon; Hayes, Kim F

    2013-11-01

    The pH impact on reductive dechlorination of cis-dichloroethylene (cis-DCE) was investigated using in situ Fe precipitates formed under iron-rich sulfate-reducing conditions. The dechlorination rate of cis-DCE increased with pH, which was attributed to changes in the solid-phase Fe concentration, the composition of Fe minerals, and the surface speciation of Fe minerals. With increasing pH, larger quantities of Fe minerals, having much greater reactivity than dissolved Fe(II), were produced. Fe-K edge X-ray absorption spectroscopy (XAS) analysis of Fe precipitates revealed the presence of multiple Fe phases with their composition varying with pH. Correlation analyses were performed to examine how the solid-phase Fe concentration, the composition of Fe minerals, and their surface speciation were linked with the cis-DCE dechlorination rate. Such analyses revealed that neither mackinawite (FeS) nor magnetite (Fe3O4) was reactive with cis-DCE dechlorination, but that Fe (oxyhydr)oxides including green rusts and Fe(OH)2 were reactive. Based on a proposed model of the surface acidity of Fe minerals, the increasing deprotonated surface Fe(II) groups with pH correlated well with the enhanced cis-DCE dechlorination. PMID:24074816

  8. Influence of nutrient amendments on the phytoextraction of weathered 2,2-bis(p-chlorophenyl)-1,1-dichloroethylene by cucurbits.

    PubMed

    White, Jason C; Parrish, Zakia D; Isleyen, Mehmet; Gent, Martin P N; Iannucci-Berger, William; Eitzer, Brian D; Mattina, Maryjane Incorvia

    2005-04-01

    Field experiments were conducted to determine the impact of nutrient amendments on the phytoextraction of weathered 2,2-bis(p-chlorophenyl)-1,1-dichloroethylene (p,p '-DDE) by eight cultivars of cucurbits over a single growing season. Four cultivars of Cucurbita pepo ssp pepo are accumulators and extract percent level quantities of persistent organic pollutants (POPs), whereas C. pepo ssp ovifera and Cucumis sativus are nonaccumulators. The nonamended accumulators phytoextracted 1.0% of the p,p'-DDE and had a translocation factor of 0.44; however, the nonaccumulators removed 0.16% of the contaminant and had a translocation factor value of 0.09. The accumulators also had 3.8 times greater inorganic element content than the nonaccumulators. Duplicate mounds of each cultivar also received weekly nutrient amendments of phosphorus (400 mg/L K2HPO4), nitrogen (200 mg/L KNO3), or nitrogen/phosphorus (400 mg/L K2HPO4, 200 mg/L KNO3); a minus phosphorus treatment involved a 1-L addition of 1 g/L AlSO4 to the soil before planting. When normalized to respective control values (unamended vegetation), the root and stem p,p'-DDE bioconcentration factors (BCF) of the accumulator cultivars were significantly greater than those of the nonaccumulator cultivars under most nutrient regimes. The biomass of accumulator cultivars decreased by up to 61% under certain nutrient regimes, resulting in mixed effects on the amount of p,p'-DDE extracted. Treatment with N and P increased nonaccumulator biomass by 40 to 100%, and increased p,p'-DDE extraction from soil by 75%. Although generally assumed that fertilizer amendments will enhance phytoremediation, as evidenced here by the nonaccumulators, additions of macronutrients may reduce the phytoextraction of weathered POPs by C. pepo ssp pepo. These findings support our hypothesis that the ability of C. pepo ssp pepo to remove sequestered organic contaminants is governed by unique nutrient-acquisition mechanisms. PMID:15839575

  9. Results of Remediation and Verification Sampling for the 600-270 Horseshoe Landfill

    SciTech Connect

    W. S. Thompson

    2005-12-14

    This report presents the results of the 2005 remedial action and verification soil sampling conducted at the 600-270 waste site after removal of soil containing residual concentrations of dichlorodiphenyl trichloroethane and its breakdown products dichlorodiphenyl dichloroethylene and dichlorodiphenyl dichloroethane. The remediation was performed in response to post-closure surface soil sampling performed between 1998 and 2003 that indicated the presence of residual DDT contamination exceeding the Record of Decision for the 1100 Area National Priorities List site cleanup criteria of 1 mg/kg that was established for the original 1994 cleanup activities.

  10. Effect of species differences, pollutant concentration, and residence time in soil on the bioaccumulation of 2,2-bis (p-chlorophenyl)-1,1-dichloroethylene by three earthworm species.

    PubMed

    Kelsey, Jason W; Colino, Allison; White, Jason C

    2005-03-01

    Laboratory experiments were conducted to study the effects of species differences, soil concentration, and contaminant-residence time in soil on the bioaccumulation factor (BAF; dry-weight ratio of contaminant concentration in the tissue to that in the soil) of 2,2-bis (p-chlorophenyl)- 1,1-dichloroethylene (p,p'-DDE) for three species of earthworms. In four field-weathered soils, the BAF for Eisenia foetida, an epigeic species (surface habitat), was approximately 10-fold higher than those for Lumbricus terrestris, an anecic species (deep habitat) and Aporrectodea caliginosa, an endogeic species (habitat within the soil profile). Preliminary analysis indicates that BAF may decline with increasing pollutant concentration in soil. With regard to contaminant-residence time, the BAF for E. foetida was lower in weathered soils relative to that in freshly amended soils, but age of p,p'-DDE did not significantly alter the BAF for A. caliginosa. These data suggest total chemical concentration alone is not a reliable indicator of the toxicological significance of a contaminated soil and that species-specific differences and environmental factors significantly impact overall exposure and risk. PMID:15779772

  11. Kinetic and inhibition studies for the aerobic cometabolism of 1,1,1-trichloroethane, 1,1-dichloroethylene, and 1,1-dichloroethane by a butane-grown mixed culture.

    PubMed

    Kim, Young; Arp, Daniel J; Semprini, Lewis

    2002-12-01

    Batch kinetic and inhibition studies were performed for the aerobic cometabolism of 1,1,1-trichloroethane (1,1,1-TCA), 1,1-dichloroethylene (1,1-DCE), and 1,1-dichloroethane (1,1-DCA) by a butane-grown mixed culture. These chlorinated aliphatic hydrocarbons (CAHs) are often found together as cocontaminants in groundwater. The maximum degradation rates (k(max)) and half-saturation coefficients (K(s)) were determined in single compound kinetic tests. The highest k(max) was obtained for butane (2.6 micromol/mg TSS/h) followed by 1,1-DCE (1.3 micromol/mg TSS/h), 1,1-DCA (0.49 micromol/mg TSS/h), and 1,1,1-TCA (0.19 micromol/mg TSS/h), while the order of K(s) from the highest to lowest was 1,1-DCA (19 microM), butane (19 microM), 1,1,1-TCA (12 microM) and 1,1-DCE (1.5 microM). The inhibition types were determined using direct linear plots, while inhibition coefficients (K(ic) and K(iu)) were estimated by nonlinear least squares regression (NLSR) fits to the kinetic model of the identified inhibition type. Two different inhibition types were observed among the compounds. Competitive inhibition among CAHs was indicated from direct linear plots, and the CAHs also competitively inhibited butane utilization. 1,1-DCE was a stronger inhibitor than the other CAHs. Mixed inhibition of 1,1,1-TCA, 1,1-DCA, and 1,1-DCE transformations by butane was observed. Thus, both competitive and mixed inhibitions are important in cometabolism of CAHs by this butane culture. For competitive inhibition between CAHs, the ratio of the K(s) values was a reasonable indicator of competitive inhibition observed. Butane was a strong inhibitor of CAH transformation, having a much lower inhibition coefficient than the K(s) value of butane, while the CAHs were weak inhibitors of butane utilization. Model simulations of reactor systems where both the growth substrate and the CAHs are present indicate that reactor performance is significantly affected by inhibition type and inhibition coefficients. Thus

  12. Methylsulfone polychlorinated biphenyl and 2,2-bis(chlorophenyl)-1,1-dichloroethylene metabolites in beluga whale (Delphinapterus leucas) from the St. Lawrence River estuary and western Hudson Bay, Canada

    SciTech Connect

    Letcher, R.J.; Norstrom, R.J.; Muir, D.C.G.; Sandau, C.D.; Koczanski, K.; Michaud, R.; De Guise, S.; Beland, P.

    2000-05-01

    Knowledge is limited regarding methylsulfone (MeSO{sub 2})-polychlorinated biphenyl (PCB), and especially MeSo{sub 2}-2,2-bis(chlorophenyl)-1,1-dichloroethylene (DDE), metabolites in cetacean species. The authors hypothesized that the ability of beluga whale (Delphinapterus leucas) to biotransform PCB and DDE compounds, and to form and degrade their MeSO{sub 2}-PCB and -DDE metabolites, is related to the capacity for xenobiotic metabolism. Adipose biopsies were collected from male and female beluga whale from distinct populations in the St. Lawrence River estuary (STL) and western Hudson Bay (WHB), Canada, which are contrasted by the exposure to different levels of cytochrome P450 enzyme-inducing, chlorinated hydrocarbon contaminants. The PCBs, DDTs, DDEs, 28 MeSO{sub 2} metabolites of 14 meta-para chlorine-unsubstituted PCBs, and four MeSO{sub 2} metabolites of 4,4{prime}- and 2,4{prime}-DDE were determined. The mean concentrations of total ({Sigma}-) MeSO{sub 2}-PCB in male STL beluga (230 ng/g), and ratios of {Sigma}-MeSO{sub 2}-PCB to {Sigma}-PCB (0.05) and {Sigma}-precursor-PCB (0.17) were approximately twofold higher, whereas the {Sigma}-precursor-PCB to {Sigma}-PCB ratio was approximately twofold lower, than in male WHB beluga. Both populations had a low formation capacity for MeSO{sub 2}-PCBs with {le} six chlorines (<4% of {Sigma}-MeSO{sub 2}-PCBs). The congener patterns were dominated by trichloro- and tetrachloro-MeSO{sub 2}-PCBs, and tetrachloro- and pentachloro-MeSO{sub 2}-PCBs in WHB and STL animals, respectively. In addition to 2- and 3-MeSO{sub 2}-4,4{prime}-DDE, two unknown MeSO{sub 2}-2,4{prime}-DDEs were detected. The mean 3-MeSO{sub 2}-4,4{prime}-DDE concentration in STL beluga (1.2 ng/g) was much greater than in WHB animals. The concentrations of 4,4{prime}-DDE, and not 3-MeSO{sub 2}-4,4{prime}-DDE, increased with age in male STL animals. The authors demonstrated that sulfone formation and clearance is related to metabolic capacity, and thus

  13. ABIOTIC NATURAL ATTENUATION OF CIS-DICHLOROETHYLENE AND 1,1-DICHLOROETHYLENE IN AQUIFER SEDIMENT

    EPA Science Inventory

    The disposal of TCE and 1,1,1-TCA at the Twin Cities Army Ammunition Plant (TCAAP) in Minnesota produced a plume of contaminated ground water that was over eight kilometers long. Although the size of the plume was consistent with a high ground water velocity in the aquifer and t...

  14. NON-BIOLOGICAL REMOVAL OF CIS-DICHLOROETHYLENE AND 1.1-DICHLOROETHYLENE IN AQUIFER SEDIMENT CONTAINING MAGNETITE

    EPA Science Inventory

    Reductive dechlorination could not explain the removal of cis-DCE, and 1,1-DCE from a plume of contaminated ground water in Minnesota. To identify the processes responsible for removal, laboratory microcosms were constructed with sediment from the aquifer near the source of the ...

  15. Time trends of persistent organic pollutants and heavy metals in umbilical cord blood of Inuit infants born in Nunavik (Québec, Canada) between 1994 and 2001.

    PubMed Central

    Dallaire, Frédéric; Dewailly, Eric; Muckle, Gina; Ayotte, Pierre

    2003-01-01

    Inuit inhabitants of Nunavik (northern Québec, Canada) consume great quantities of marine food and are therefore exposed to high doses of food chain contaminants. In this study, we report the time trends of persistent organic pollutants, mercury, and lead in umbilical cord blood of infants from three communities of the east coast of Hudson Bay in Nunavik. We analyzed 251 cord blood samples collected from 1994 through 2001 for polychlorinated biphenyls (PCBs), dichlorodiphenyl trichloroethane (DDT), dichlorodiphenyl dichloroethylene (DDE), hexachlorobenzene (HCB), chlordanes, lead, and mercury. Using an exponential model, we found strongly significant decreasing trends for PCBs (7.9% per year, p < 0.001), DDE (9.1% per year, p < 0.001), DDT (8.2% per year, p < 0.001), and HCB (6.6% per year, p < 0.01). No significant trends were detected for chlordanes. A significant reduction of lead and mercury concentrations was found, but there was no clear linear or exponential trend. The decreases observed could be explained by a decrease in food contamination, by changes in dietary habits, or, most likely, by a combination of both. PMID:14527847

  16. Evaluation of pesticide residues in human blood samples from Punjab (India)

    PubMed Central

    Bedi, Jasbir Singh; Gill, J. P. S.; Kaur, P.; Sharma, A.; Aulakh, R. S.

    2015-01-01

    Aim: The present study was undertaken to estimate the current status of residues of organochlorine pesticides (OCPs), organophosphates (OPs) and synthetic pyrethroids (SPs) pesticides in human blood. Materials and Methods: Human blood samples were analyzed by gas chromatography and confirmed by gas chromatography-mass spectrometry in selective ion monitoring mode. Results: The gas chromatographic analysis of human blood samples collected from Punjab revealed the presence of p,p’-dichlorodiphenyl dichloroethylene (DDE), p,p’ dichlorodiphenyl dichloroethane (DDD), o,p’ DDE and β-endosulfan at mean levels of 15.26, 2.71, 5.62 and 4.02 ng/ml, respectively. p,p’ DDE residue was observed in 18.0% blood samples, and it contributes 55% of the total pesticide burden in human blood. The difference of total dichlorordiphenyl trichloroethane (DDT) between different age groups of humans was found to be statistically significant (p<0.05). The difference of DDT and endosulfan between dietary habits, gender and spraying of pesticides was found statistically non-significant, however endosulfan residues were observed only in pesticide sprayer’s population. Conclusion: Occurrence of p,p’ DDE, p,p’ DDD, o,p’ DDE in human blood indicated restricted use of DDT. However, presence of endosulfan residues in occupationally exposed population is a matter of public health concern. PMID:27046999

  17. MISCANTHUS X GIGANTEUS AS A NEW HIGHLY EFFICIENT PHYTOREMEDIATION AGENT FOR IMPROVING SOILS CONTAMINATED BY PESTICIDES RESIDUES AND SUPPLEMENTED CONTAMINANTS.

    PubMed

    Nurzhanova, A; Pidlisnyuk, V; Kalugin, S; Stefanovska, T; Drimal, M

    2015-01-01

    Soil monitoring was accomplished at 76 former pesticide storehouses in Kazakhstan. Gas chromatography analysis was limited to the organochlorine pesticides DDT (p,p'-dichloro-diphenyl-trichloroethane) and HCH (hexachlorocyclohexane), and their associated metabolites and isomers: 2.4'-DDD (p,p'-dichlorodiphenyl dichloroethane); 4.4'-DDD; 4.4'-DDT; 4.4'-DDE (p,p'-dichlorodiphenyl-dichloroethylene); α-HCH; β-HCH and γ-HCH. The studies showed exceeding of Maximum Acceptable Concentration (MAC) by 10 times at soil samples taken at 24 former pesticide storehouses, and the basic pollutants were isomers of α-HCH, β-HCH and metabolite of 4.4'-DDE, 4.4'-DDT, supplemented by heavy metals. Monitoring data demonstrated the potential ecological danger and health risk posed by the sites, especially those located near populated areas. In order to eliminate the negative environmental and health effect it was proposed to use phytotechnology with second generation biofuel crop Miscanthus x giganteus. The technology applied directly at the contaminated area (in situ), helping to decrease costs and to reduce exposure from polluted sites. The plant shows good growing at the soil contaminated by pesticides during vegetation season. PMID:27141732

  18. ABIOTIC NATURAL ATTENUATION OF CIS-DISHLOROETHYLENE AND 1,1-DICHLOROETHYLENE IN AQUIFER SEDIMENT

    EPA Science Inventory

    The disposal of TCE and 1,1,1-TCA at the Twin Cities Army Ammunition Plant (TCAAP) in Minnesota produced a plume of contaminated ground water that was over eight kilometers long. Although the size of the plume was consistent with a high ground water velocity in the aquifer and t...

  19. Prenatal DDT and DDE exposure and child IQ in the CHAMACOS cohort.

    PubMed

    Gaspar, Fraser W; Harley, Kim G; Kogut, Katherine; Chevrier, Jonathan; Mora, Ana Maria; Sjödin, Andreas; Eskenazi, Brenda

    2015-12-01

    Although banned in most countries, dichlorodiphenyl-trichloroethane (DDT) continues to be used for vector control in some malaria endemic areas. Previous findings from the Center for the Health Assessment of Mothers and Children of Salinas (CHAMACOS) cohort study found increased prenatal levels of DDT and its breakdown product dichlorodiphenyl-dichloroethylene (DDE) to be associated with altered neurodevelopment in children at 1 and 2years of age. In this study, we combined the measured maternal DDT/E concentrations during pregnancy obtained for the prospective birth cohort with predicted prenatal DDT and DDE levels estimated for a retrospective birth cohort. Using generalized estimating equation (GEE) and linear regression models, we evaluated the relationship of prenatal maternal DDT and DDE serum concentrations with children's cognition at ages 7 and 10.5years as assessed using the Full Scale Intelligence Quotient (IQ) and 4 subtest scores (Working Memory, Perceptual Reasoning, Verbal Comprehension, and Processing Speed) of the Wechsler Intelligence Scale for Children (WISC). In GEE analyses incorporating both age 7 and 10.5 scores (n=619), we found prenatal DDT and DDE levels were not associated with Full Scale IQ or any of the WISC subscales (p-value>0.05). In linear regression analyses assessing each time point separately, prenatal DDT levels were inversely associated with Processing Speed at age 7years (n=316), but prenatal DDT and DDE levels were not associated with Full Scale IQ or any of the WISC subscales at age 10.5years (n=595). We found evidence for effect modification by sex. In girls, but not boys, prenatal DDE levels were inversely associated with Full Scale IQ and Processing Speed at age 7years. We conclude that prenatal DDT levels may be associated with delayed Processing Speed in children at age 7years and the relationship between prenatal DDE levels and children's cognitive development may be modified by sex, with girls being more adversely

  20. Mechanisms, chemistry, and kinetics of anaerobic biodegradation of cis-dichloroethylene and vinyl chloride. 1998 annual progress report

    SciTech Connect

    McCarty, P.L.; Spormann, A.M.

    1998-06-01

    'The objectives of this study are to: (1) determine the biochemical pathways for reductive dehalogenation of cis-1,2-dichloroethene (cDCE) and vinyl chloride (VC), including identification of the enzymes involved, (2) determine the chemical requirements, especially the type and quantity of electron donors needed by the microorganisms for reductive dehalogenation, and (3) evaluate the kinetics of the process with respect to the concentration of both the electron donors and the electron acceptors (cDCE and VC). Progress has been made under each of the three primary objectives. One manuscript related to the first objective has been published. Manuscripts related to the other two objectives have been submitted for publication. Findings related to the three objectives are summarized.'

  1. Mechanisms, chemistry and kinetics of the anaerobic biodegradation of cis-dichloroethylene and vinyl chloride. First annual progress report, September 15, 1996--September 14, 1997

    SciTech Connect

    McCarty, P.L.; Spormann, A.

    1997-01-01

    'This three-year project is to study the anaerobic biological conversion of cis-1,2- dichloroethene (cDCE) and vinyl Chloride (VC) to ethene. The study is being conducted in three separate phases, the first to better understand the mechanisms involved in cDCE and VC biodegradation, the second to evaluate the chemistry of the processes involved, and the third, to study factors affecting reaction kinetics. Major funding is being provided by the US Department of Energy, but the DuPont Chemical Company has also agreed to directly cost-share on the project at a rate of $75,000 per year for the three year period. Tetrachloroethylene (PCE) and trichloroethylene (TCE) are solvents that are among the most widely occurring organic groundwater contaminants. The biological anaerobic reduction-of chlorinated aliphatic hydrocarbons (CAHs) such as PCE and TCE to cDCE and VC in groundwater was reported in the early 1980s. Further reduction of PCE and its intermediates to ethene was reported in 1989. Several pure cultures of anaerobic bacteria have been found to reductively dehalogenate PCE to cDCE Rates of reduction of PCE and TCE to cDCE are high and the need for electron donor addition for the reactions is small. However, the subsequent reduction of cDCE to VC, and then of VC to the harmless end product, ethene, is much slower and only recently has a pure culture been reported that is capable of reducing cDCE to VC or VC to ethene. There are numerous. reports of such conversions in mixed cultures. The reduction of cDCE and VC to ethene is where basic research is most needed and is the subject of this study.'

  2. INTERACTION BETWEEN WATER POLLUTANTS: QUANTITATIVE ELECTRON MICROSCOPY OF HEPATIC MORPHOLOGICAL CHANGES INDUCED BY 1,2-DICHLOROETHANE (DCE) AND 1,1-DICHLOROETHYLENE (VDC)

    EPA Science Inventory

    Numerous chemicals are found as contaminants in public water supplies which constitute potential public health hazards. The studies here were designed to determine the early histopathological effects of two known water contaminants, 1,2-dichloroethane (DCE) and 1,1-dichloroethyle...

  3. Multi-species interactions impact the accumulation of weathered 2,2-bis (p-chlorophenyl)-1,1-dichloroethylene (p,p'-DDE) from soil.

    PubMed

    Kelsey, Jason W; White, Jason C

    2005-09-01

    The impact of interactions between the earthworms Eisenia foetida and Lumbricus terrestris and the plants Cucurbita pepo and Cucurbita maxima on the uptake of weathered p,p'-DDE from soil was determined. Although some combinations of earthworm and plant species caused significant changes in the p,p'-DDE burden in both organisms, the effects were species specific. Contaminant bioconcentration in C. pepo was increased slightly by E. foetida and by 3-fold when the plant was grown with L. terrestris. E. foetida had no effect on the contaminant BCF by C. maxima, but L. terrestris caused a 2-fold reduction in p,p'-DDE uptake by the plant. Contaminant levels in E. foetida and L. terrestris were unaffected by C. pepo. When grown with C. maxima, the concentration of p,p'-DDE decreased by approximately 4-fold and 7-fold in E. foetida and L. terrestris, respectively. The data suggest that the prediction of contaminant bioavailability should consider interactions among species. PMID:15913856

  4. Screening for estrogen and androgen receptor activities in 200 pesticides by in vitro reporter gene assays using Chinese hamster ovary cells.

    PubMed Central

    Kojima, Hiroyuki; Katsura, Eiji; Takeuchi, Shinji; Niiyama, Kazuhito; Kobayashi, Kunihiko

    2004-01-01

    We tested 200 pesticides, including some of their isomers and metabolites, for agonism and antagonism to two human estrogen receptor (hER) subtypes, hERalpha and hERbeta, and a human androgen receptor (hAR) by highly sensitive transactivation assays using Chinese hamster ovary cells. The test compounds were classified into nine groups: organochlorines, diphenyl ethers, organophosphorus pesticides, pyrethroids, carbamates, acid amides, triazines, ureas, and others. These pesticides were tested at concentrations < 10-5 M. Of the 200 pesticides tested, 47 and 33 showed hER- and hERbeta-mediated estrogenic activities, respectively. Among them, 29 pesticides had both hERalpha and hERbeta agonistic activities, and the effects of the organochlorine insecticides beta-benzene hexachloride (BHC) and delta-BHC and the carbamate insecticide methiocarb were predominantly hERbeta rather than hERalpha agonistic. Weak antagonistic effects toward hERalpha and hERbeta were shown in five and two pesticides, respectively. On the other hand, none of tested pesticides showed hAR-mediated androgenic activity, but 66 of 200 pesticides exhibited inhibitory activity against the transcriptional activity induced by 5alpha-dihydrotestosterone. In particular, the antiandrogenic activities of two diphenyl ether herbicides, chlornitrofen and chlomethoxyfen, were higher than those of vinclozolin and p,p -dichlorodiphenyl dichloroethylene, known AR antagonists. The results of our ER and AR assays show that 34 pesticides possessed both estrogenic and antiandrogenic activities, indicating pleiotropic effects on hER and hAR. We also discussed chemical structures related to these activities. Taken together, our findings suggest that a variety of pesticides have estrogenic and/or antiandrogenic potential via ER and/or AR, and that numerous other manmade chemicals may also possess such estrogenic and antiandrogenic activities. PMID:15064155

  5. FIELD EVALUATION OF IN SITU AEROBIC COMETABOLISM OF TRICHLOROETHYLENE AND THREE DICHLOROETHYLENE ISOMERS USING PHENOL AND TOLUENE AS THE PRIMARY SUBSTRATES. (R825689C050,R825689C066)

    EPA Science Inventory

    The perspectives, information and conclusions conveyed in research project abstracts, progress reports, final reports, journal abstracts and journal publications convey the viewpoints of the principal investigator and may not represent the views and policies of ORD and EPA. Concl...

  6. Analysis of organochlorine pesticides in coral (Porites evermanni) samples using accelerated solvent extraction and gas chromatography/ion trap mass spectrometry.

    PubMed

    Wang, Dongli; Miao, Xiusheng; Li, Qing X

    2008-02-01

    A gas chromatography/ion trap mass spectrometry method was developed for analysis of organochlorine pesticides (OCPs) in coral samples, which were extracted with accelerated solvent extraction (ASE) and cleaned up on a sulfuric acid-modified silica gel column. The optimal ASE conditions were found to be 100 degrees C and 2000 psi, with a mixture of acetone and methylene chloride (1:1, v/v). The target analytes include hexachlorocyclohexanes (HCHs, specifically, alpha-, beta-, gamma-, and delta-HCH isomers), heptachlor, and hexachlorobenzene (HCB), o,p'-, p,p'-dichlorodiphenyltrichloroethane (o,p'-, p,p'-DDT), o,p'-, p,p'-dichlorodiphenyl-dichloroethylene (o,p'-, p,p'-DDE), and o,p'-, p,p'-dichlorodiphenyldichloroethane (o,p'-, p,p'-DDD). Standard sand samples were used as an alternative matrix spiked with OCP standards to determine the method precision and accuracy. Average recoveries of OCPs ranged from 82% to 102%, with relative standard deviations (RSDs) of 3%-6%, at a level of 10 ng/g and from 50% to 68%, with RSDs of 13%-19% at a level of 2 ng/g. The developed method was applied for analysis of OCPs in coral samples collected from Tern Island and Bikini Atoll in the Pacific Ocean. The concentrations of HCB were 7-26 pg/g dry weight in the samples from Bikini Atoll and 3-45 pg/g in those from Tern Island, and heptachlor concentrations were 208-2200 and 44-104 pg/g in the coral samples from Bikini Atoll and Tern Island, respectively. (summation operator)HCH (sum of alpha-, beta-, gamma-, and delta-HCH) were 8-82 pg/g in Bikini Atoll coral and 86-629 pg/g in Tern island coral, and (summation operator)DDT (sum of o,p'-, p,p'-DDD, o,p'-, p,p'-DDE, and o,p'- p,p'-DDT) were 80-212 pg/g in Bikini Atoll coral and 593-3165 pg/g in Tern Island coral. The results suggest that coral is a viable indicator species for pollution monitoring, which pollutants and their concentrations may be related to dated carbonate layers. PMID:17721673

  7. Food safety.

    PubMed

    Borchers, Andrea; Teuber, Suzanne S; Keen, Carl L; Gershwin, M Eric

    2010-10-01

    Food can never be entirely safe. Food safety is threatened by numerous pathogens that cause a variety of foodborne diseases, algal toxins that cause mostly acute disease, and fungal toxins that may be acutely toxic but may also have chronic sequelae, such as teratogenic, immunotoxic, nephrotoxic, and estrogenic effects. Perhaps more worrisome, the industrial activities of the last century and more have resulted in massive increases in our exposure to toxic metals such as lead, cadmium, mercury, and arsenic, which now are present in the entire food chain and exhibit various toxicities. Industrial processes also released chemicals that, although banned a long time ago, persist in the environment and contaminate our food. These include organochlorine compounds, such as 1,1,1-trichloro-2,2-bis(p-chlorophenyl)ethane (dichlorodiphenyl dichloroethene) (DDT), other pesticides, dioxins, and dioxin-like compounds. DDT and its breakdown product dichlorophenyl dichloroethylene affect the developing male and female reproductive organs. In addition, there is increasing evidence that they exhibit neurodevelopmental toxicities in human infants and children. They share this characteristic with the dioxins and dioxin-like compounds. Other food contaminants can arise from the treatment of animals with veterinary drugs or the spraying of food crops, which may leave residues. Among the pesticides applied to food crops, the organophosphates have been the focus of much regulatory attention because there is growing evidence that they, too, affect the developing brain. Numerous chemical contaminants are formed during the processing and cooking of foods. Many of them are known or suspected carcinogens. Other food contaminants leach from the packaging or storage containers. Examples that have garnered increasing attention in recent years are phthalates, which have been shown to induce malformations in the male reproductive system in laboratory animals, and bisphenol A, which negatively

  8. Multiple adverse thyroid and metabolic health signs in the population from the area heavily polluted by organochlorine cocktail (PCB, DDE, HCB, dioxin)

    PubMed Central

    Langer, Pavel; Kočan, Anton; Tajtáková, Mária; Sušienková, Katarína; Rádiková, Žofia; Koška, Juraj; Kšinantová, Lucia; Imrich, Richard; Hučková, Miloslava; Drobná, Beáta; Gašperíková, Daniela; Trnovec, Tomáš; Klimeš, Iwar

    2009-01-01

    Background Several our previous studies showed associations of increasing blood level of persistent organochlorinated pollutants (POPs) with individual thyroid and metabolic adverse health signs in subjects from heavily polluted area (POLL) compared to these from the area of background pollution (BCGR). In this study we present increasing number of subjects with multiple adverse signs positively associated with blood level of polychlorinated biphenyls (PCBs) which is used as a marker of other POPs cocktail. Methods In a total of 2046 adults (834 males and 1212 females; age range 21–75) from POLL and BCGR the serum level of major POPs such as of 15 most abundant PCBs congeners, dichlorodiphenyl-dichloroethylene (p,p'-DDE) and hexachlorobenzene (HCB) was estimated by high resolution gas chromatography. In addition, the data on thyroid volume by ultrasound and body mass index were obtained and serum level of thyroperoxidase and thyrotropin receptor antibodies as well as that of free thyroxine, total triiodothyronine, thyrotropin, thyroglobulin, fasting glucose and insulin, cholesterol and triglycerides was measured. Thus, a total of 13 adverse signs were defined and the interrelations between PCBs level and increasing number of subjects with increasing number of adverse signs were evaluated. Results Because of high correlation between major POPs (PCB, DDE and HCB), for this purpose the level of PCBs was considered as a marker also for the presence of DDE and HCB. Thus, if all data obtained from 2046 subjects were stratified according to quintiles of PCBs level, highly significant increase was found (p < 0.02 to 0.0000 by chi-sqauare) for the frequency of 8 among 13 signs, while the increase of one additional sign was slightly above significance limit and that in 4 other was not significant. Also the number of subjects with multiple adverse signs was significantly higher in POLL than in BCGR. For instance, in BCGR area (1038 subjects; median PCB level of 744 ng/g and

  9. MICROCOSM AND IN-SITU FIELD STUDIES OF ENHANCED BIOTRANSFORMATION OF TRICHLOROETHYLENE BY PHENOL-UTILIZING MICROORGANISMS

    EPA Science Inventory

    The ability of different aerobic groundwater microorganisms to cometabolically degrade trichloroethylene (TCE), 1,2-cis-dichloroethylene (c-DCE), and 1,2-trans-dichloroethylene (t-DCE) was evaluated both in groundwater-fed microcosms and in situ in a shallow aquifer. Microcosms a...

  10. Potential occupational exposures in the Reiss-Engelhorn-Museen Mannheim/Germany.

    PubMed

    Musshoff, Frank; Gottsmann, Sandra; Mitschke, Sylvia; Rosendahl, Wilfried; Madea, Burkhard

    2010-12-01

    The Reiss-Engelhorn-Museen in Mannheim, Germany requested support from a toxicological laboratory in evaluating occupational exposures before a cleanup and renovation period in 2006. Samples of dust and dirt and scrapings of exhibits were collected from several locations. Following toxicologically relevant compounds could be identified by gas chromatography - mass spectrometry (GC/MS) by comparison with a mass spectra library: dichlorodiphenyl trichloroethane (DDT) and its breakdown product dichlorodiphenyl dichloroethane (DDD) as well as dichlorodiphenyl dichlorethylene (DDE), methoxychlor, nicotine, and camphor. In recent times various insecticides have been used to protect museum artefacts against moths, woodborers and other insect pests. Caution has to be made because the presence of hazardous compounds can result in security problems for museum staff as well as for visitors. PMID:20972535

  11. Chemical contaminants, pharmacokinetics, and the lactating mother.

    PubMed Central

    Rogan, W J; Ragan, N B

    1994-01-01

    We review the commonly occurring persistent pesticides and industrial chemicals in breast milk. These chemicals are dichlorodiphenyl trichloroethane as dichlorodiphenyl dichloroethene dieldrin, chlordane as oxychlordane, heptachlor, polychlorinated biphenyls, polychlorinated dibenzofurans, and polychlorinated dibenzodioxins. We present a worked example of the kinds of pharmacokinetic assumptions and calculations necessary for setting regulatory limits of contaminants in the food supply, calculating dose of chemical contaminants to the nursed infant, converting risks from lifetime exposure in laboratory animals to risks for short-term exposure in humans, and estimating the excess cancer risk to the nursed infant. PMID:7737048

  12. 40 CFR Table 2 to Subpart Ggg of... - Partially Soluble HAP

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ...,4-) Chlorobenzene Trichloroethylene Chloroethane (ethyl chloride) Trimethylpentane Vinyl acetate Xylene (p) Vinyl chloride N-hexane Xylene (m) Xylene (o) ...-Tetrachloroethane Chloromethane 1,1,2-Trichloroethane Chloroprene 1,1-Dichloroethylene (vinylidene chloride)...

  13. MICROEMULSION OF MIXED CHLORINATED SOLVENTS USING FOOD GRADE (EDIBLE) SURFACTANTS

    EPA Science Inventory

    Ground water contamination frequently consists of mixed chlorinated solvents [e.g., tetrachloroethylene (PCE), trichloroethylene (TCE), and trans-1,2- dichloroethylene (DCE)]. In this research, mixtures of the food grade (edible) surfactants bis(2-ethylhexyl) sodium sulfosuccinat...

  14. 40 CFR 465.02 - General definitions.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... the definitions set forth in 40 CFR part 401, the following definitions apply to this part: (a) “Coil...-chloroethyl) ether Chloroform 1,1-Dichloroethylene Methylene chloride (dichloromethane) Pentachlorophenol...

  15. 40 CFR 465.02 - General definitions.

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... addition to the definitions set forth in 40 CFR part 401, the following definitions apply to this part: (a...-chloroethyl) ether Chloroform 1,1-Dichloroethylene Methylene chloride (dichloromethane) Pentachlorophenol...

  16. 40 CFR 465.02 - General definitions.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... addition to the definitions set forth in 40 CFR part 401, the following definitions apply to this part: (a...-chloroethyl) ether Chloroform 1,1-Dichloroethylene Methylene chloride (dichloromethane) Pentachlorophenol...

  17. 40 CFR Table 2 to Subpart Jj of... - List of Volatile Hazardous Air Pollutants

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... Chloroform 67663 Chloromethyl methyl ether 107302 Chloroprene 126998 Cresols (isomers and mixture) 1319773 o...-Dichloroethylene) 75354 Xylenes (isomers and mixture) 1330207 o-Xylene 95476 m-Xylene 108383 p-Xylene 106423...

  18. 40 CFR Table 2 to Subpart Jj of... - List of Volatile Hazardous Air Pollutants

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... Chloroform 67663 Chloromethyl methyl ether 107302 Chloroprene 126998 Cresols (isomers and mixture) 1319773 o...-Dichloroethylene) 75354 Xylenes (isomers and mixture) 1330207 o-Xylene 95476 m-Xylene 108383 p-Xylene 106423...

  19. 40 CFR Table 2 to Subpart Jj of... - List of Volatile Hazardous Air Pollutants

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... Chloroform 67663 Chloromethyl methyl ether 107302 Chloroprene 126998 Cresols (isomers and mixture) 1319773 o...-Dichloroethylene) 75354 Xylenes (isomers and mixture) 1330207 o-Xylene 95476 m-Xylene 108383 p-Xylene 106423...

  20. 40 CFR Table 2 to Subpart Jj of... - List of Volatile Hazardous Air Pollutants

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... Chloroform 67663 Chloromethyl methyl ether 107302 Chloroprene 126998 Cresols (isomers and mixture) 1319773 o...-Dichloroethylene) 75354 Xylenes (isomers and mixture) 1330207 o-Xylene 95476 m-Xylene 108383 p-Xylene 106423...

  1. Biodegradation of trichloroethylene by Methylosinus trichosporium OB3b.

    PubMed Central

    Tsien, H C; Brusseau, G A; Hanson, R S; Waclett, L P

    1989-01-01

    The methanotroph Methylosinus trichosporium OB3b, a type II methanotroph, degraded trichloroethylene at rates exceeding 1.2 mmol/h per g (dry weight) following the appearance of soluble methane monooxygenase in continuous and batch cultures. Cells capable oxidizing trichloroethylene contained components of soluble methane monooxygenase as demonstrated by Western blot (immunoblot) analysis with antibodies prepared against the purified enzyme. Growth of cultures in a medium containing 0.25 microM or less copper sulfate caused derepression of the synthesis of soluble methane monooxygenase. In these cultures, the specific rates of methane and methanol oxidation did not change during growth, while trichloroethylene oxidation increased with the appearance of soluble methane monooxygenase. M. trichosporium OB3b cells that contained soluble methane monooxygenase also degraded vinyl chloride, 1,1-dichloroethylene, cis-1,2-dichloroethylene, and trans-1,2-dichloroethylene. Images PMID:2515801

  2. Fate and transport of trichloroethane and trichloroethylene contaminated groundwater, building 719, Dover Air Force Base, Delaware

    SciTech Connect

    Melchiorre, K.J.

    1996-08-01

    Trichloroethane and trichloroethylene are common chlorinated aliphatic industrial organic solvents used in degreasing operations. Both are typically found in groundwater environments as a result of leaking underground storage tanks, leachate from landfills, and contaminant migration from hazardous waste dump sites. Transformation by-products are also found in association with trichloroethane and trichloroethylene without any known source other than from reductive dechlorination. Dechlorinated by-products include 1,1-dichloroethane; cis and trans 1,2-dichloroethylene, 1,1-dichloroethylene, chloroethane, and vinyl chloride. Trichloroethane and trichloroethylene and their transformation by-products are suspected human health hazards. Vinyl chloride is a known human carcinogen, while trichloroethylene is considered a probable human carcinogen, and 1,1-dichloroethylene and 1,1-dichloroethane possible human carcinogens.

  3. In situ bioremediation of chlorinated solvents.

    PubMed Central

    Semprini, L

    1995-01-01

    Chlorinated solvents and their natural transformation products are the most frequently observed groundwater contaminants in the United States. In situ bioremediation using anaerobic or aerobic co-metabolic processes is a promising means of cleaning up contaminated aquifers. Studies show that under natural conditions trichloroethylene can be anaerobically degraded to dichloroethylene, vinyl chloride, and ethylene. Pilot scale field studies of in situ aerobic co-metabolic transformations have shown that indigenous microbes grown on phenol are more effective at degrading trichloroethylene and cis-1,2-dichloroethylene than microbes grown on methane. Modeling studies support field observations and indicate that the removal of trichloroethylene and cis-dichloroethylene results from the biostimulation of an indigenous microbial population. Field tests and modeling studies indicate that, at high TCE concentration, degradation becomes stoichiometrically limited. PMID:8565895

  4. Unraveling the Mechanism and Regioselectivity of the B12-Dependent Reductive Dehalogenase PceA.

    PubMed

    Liao, Rong-Zhen; Chen, Shi-Lu; Siegbahn, Per E M

    2016-08-22

    PceA is a cobalamin-dependent reductive dehalogenase that catalyzes the dechlorination of perchloroethylene to trichloroethylene and then to cis-dichloroethylene as the sole final product. The reaction mechanism and the regioselectivity of this enzyme are investigated by using density functional calculations. Four different substrates, namely, perchloroethylene, trichloroethylene, cis-dichloroethylene, and chlorotheylene, have been considered and were found to follow the same reaction mechanism pattern. The reaction starts with the reduction of Co(II) to Co(I) through a proton-coupled electron transfer process, with the proton delivered to a Tyr246 anion. This is followed by concerted C-Cl bond heterolytic cleavage and proton transfer from Tyr246 to the substrate carbon atom, generating a Co(III) -Cl intermediate. Subsequently, a one-electron transfer leads to the formation of the Co(II) -Cl product, from which the chloride and the dehalogenated product can be released from the active site. The substrate reactivity follows the trend perchloroethylene>trichloroethylene≫cis-dichloroethylene≫chlorotheylene. The barriers for the latter two substrates are significantly higher compared with those for perchloroethylene and trichloroethylene, implying that PceA does not catalyze their degradation. In addition, the formation of cis-dichloroethylene has a lower barrier by 3.8 kcal mol(-1) than the formation of trans-dichloroethylene and 1,1-dichloroethylene, reproducing the regioselectivity. These results agree quite well with the experimental findings, which show cis-dichloroethylene as the sole product in the PceA-catalyzed dechlorination of perchloethylene and trichloroethylene. PMID:27459105

  5. HUMORAL AND CELL-MEDIATED IMMUNE STATUS OF MICE EXPOSED TO TRANS-1,2-DICHLORO ETHYLENE

    EPA Science Inventory

    The study assessed possible adverse immunological effects of trans-1,2-dichloroethylene (DCE) on random-bred CD-1 mice following 14 and 90 days of exposure. A 14-day range-finding study was performed on male mice by gavage at doses 1/10 and 1/100 the LD50 (210 and 21 mg/kg). No a...

  6. 40 CFR Table 2 to Subpart Ggg of... - Partially Soluble HAP

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... Trichloroethylene Chloroethane (ethyl chloride) Trimethylpentane Vinyl acetate Xylene (p) Vinyl chloride N-hexane... Chloromethane 1,1,2-Trichloroethane Chloroprene 1,1-Dichloroethylene (vinylidene chloride) Cumene 1,2... Methylene chloride Allyl chloride N,N-dimethylaniline Benzene Propionaldehyde Benzyl chloride...

  7. 40 CFR Table 7 to Subpart Vvvvvv... - Partially Soluble HAP

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    .... Vinyl acetate 108054 57. Vinyl chloride 75014 58. Xylene (m) 108383 59. Xylene (o) 95476 60. Xylene (p...-Dichloroethylene (vinylidene chloride) 75354 5. 1,2-Dibromoethane 106934 6. 1,2-Dichloroethane (ethylene dichloride.... Acrolein 107028 15. Acrylonitrile 107131 16. Allyl chloride 107051 17. Benzene 71432 18. Benzyl...

  8. 40 CFR Table 7 to Subpart Vvvvvv... - Partially Soluble HAP

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    .... Vinyl acetate 108054 57. Vinyl chloride 75014 58. Xylene (m) 108383 59. Xylene (o) 95476 60. Xylene (p...-Dichloroethylene (vinylidene chloride) 75354 5. 1,2-Dibromoethane 106934 6. 1,2-Dichloroethane (ethylene dichloride.... Acrolein 107028 15. Acrylonitrile 107131 16. Allyl chloride 107051 17. Benzene 71432 18. Benzyl...

  9. 40 CFR Table 7 to Subpart Vvvvvv... - Partially Soluble HAP

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    .... Vinyl acetate 108054 57. Vinyl chloride 75014 58. Xylene (m) 108383 59. Xylene (o) 95476 60. Xylene (p...-Dichloroethylene (vinylidene chloride) 75354 5. 1,2-Dibromoethane 106934 6. 1,2-Dichloroethane (ethylene dichloride.... Acrolein 107028 15. Acrylonitrile 107131 16. Allyl chloride 107051 17. Benzene 71432 18. Benzyl...

  10. 40 CFR Table 2 to Subpart Ggg of... - Partially Soluble HAP

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... Trichloroethylene Chloroethane (ethyl chloride) Trimethylpentane Vinyl acetate Xylene (p) Vinyl chloride N-hexane... Chloromethane 1,1,2-Trichloroethane Chloroprene 1,1-Dichloroethylene (vinylidene chloride) Cumene 1,2... Methylene chloride Allyl chloride N,N-dimethylaniline Benzene Propionaldehyde Benzyl chloride...

  11. 40 CFR Table 2 to Subpart Ggg of... - Partially Soluble HAP

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... Trichloroethylene Chloroethane (ethyl chloride) Trimethylpentane Vinyl acetate Xylene (p) Vinyl chloride N-hexane... Chloromethane 1,1,2-Trichloroethane Chloroprene 1,1-Dichloroethylene (vinylidene chloride) Cumene 1,2... Methylene chloride Allyl chloride N,N-dimethylaniline Benzene Propionaldehyde Benzyl chloride...

  12. 40 CFR Table 7 to Subpart Vvvvvv... - Partially Soluble HAP

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    .... Vinyl acetate 108054 57. Vinyl chloride 75014 58. Xylene (m) 108383 59. Xylene (o) 95476 60. Xylene (p...-Dichloroethylene (vinylidene chloride) 75354 5. 1,2-Dibromoethane 106934 6. 1,2-Dichloroethane (ethylene dichloride.... Acrolein 107028 15. Acrylonitrile 107131 16. Allyl chloride 107051 17. Benzene 71432 18. Benzyl...

  13. 40 CFR Appendix I to Part 257 - Maximum Contaminant Levels (MCLs)

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... Drinking Water Act Chemical CAS No. MCL -(mg/l) Arsenic 7440-38-2 0.05 Barium 7440-39-3 1.0 Benzene 71-343... 107-06-2 0.005 1,1-Dichloroethylene 75-35-4 0.007 Endrin 75-20-8 0.0002 Fluoride 7 4.0 Lindane...

  14. 40 CFR Appendix I to Part 257 - Maximum Contaminant Levels (MCLs)

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... Drinking Water Act Chemical CAS No. MCL -(mg/l) Arsenic 7440-38-2 0.05 Barium 7440-39-3 1.0 Benzene 71-343... 107-06-2 0.005 1,1-Dichloroethylene 75-35-4 0.007 Endrin 75-20-8 0.0002 Fluoride 7 4.0 Lindane...

  15. 40 CFR Appendix I to Part 257 - Maximum Contaminant Levels (MCLs)

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... Drinking Water Act Chemical CAS No. MCL -(mg/l) Arsenic 7440-38-2 0.05 Barium 7440-39-3 1.0 Benzene 71-343... 107-06-2 0.005 1,1-Dichloroethylene 75-35-4 0.007 Endrin 75-20-8 0.0002 Fluoride 7 4.0 Lindane...

  16. 40 CFR Table 6 to Part 455 - PSES and PSNS for Priority Pollutants

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 40 Protection of Environment 29 2010-07-01 2010-07-01 false PSES and PSNS for Priority Pollutants 6 Table 6 to Part 455 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) EFFLUENT... Pollutants Pollutant Daily maximum shall not exceed Monthly maximum shall not exceed 1,1-Dichloroethylene...

  17. Reductive dechlorination of Tri- and tetrachloroethylenes depends on transition from aerobic to anaerobic conditions.

    PubMed Central

    Kästner, M

    1991-01-01

    Aerobic enrichment cultures from contaminated groundwaters dechlorinated trichloroethylene (TCE) (14.6 mg/liter; 111 mumol/liter) and tetrachloroethylene (PCE) (16.2 mg/liter; 98 mumol/liter) reductively within 4 days after the transition from aerobic to anaerobic conditions. The transformation products were equimolar amounts of cis-1,2-dichloroethylene and traces of 1,1-dichloroethylene. No other chlorinated product and no methane were detected. The change was accompanied by the release of sulfide, which caused a decrease in the redox potential from 0 to -150 mV. In sterile control experiments, sulfide led to the abiotic formation of traces of 1,1-dichloroethylene without cis-1,2-dichloroethylene production. The reductive dechlorination of PCE via TCE depended on these specific transition conditions after consumption of the electron acceptor oxygen or nitrate. Repeated feeding of TCE or PCE to cultures after the change to anaerobic conditions yielded no further dechlorination. Only aerobic subcultures with an air/liquid ratio of 1:4 maintained dechlorination activities; anaerobic subcultures showed no transformation. Bacteria from noncontaminated sites showed no reduction under the same conditions. PMID:1892393

  18. Reductive dechlorination of Tri- and tetrachloroethylenes depends on transition from aerobic to anaerobic conditions.

    PubMed

    Kästner, M

    1991-07-01

    Aerobic enrichment cultures from contaminated groundwaters dechlorinated trichloroethylene (TCE) (14.6 mg/liter; 111 mumol/liter) and tetrachloroethylene (PCE) (16.2 mg/liter; 98 mumol/liter) reductively within 4 days after the transition from aerobic to anaerobic conditions. The transformation products were equimolar amounts of cis-1,2-dichloroethylene and traces of 1,1-dichloroethylene. No other chlorinated product and no methane were detected. The change was accompanied by the release of sulfide, which caused a decrease in the redox potential from 0 to -150 mV. In sterile control experiments, sulfide led to the abiotic formation of traces of 1,1-dichloroethylene without cis-1,2-dichloroethylene production. The reductive dechlorination of PCE via TCE depended on these specific transition conditions after consumption of the electron acceptor oxygen or nitrate. Repeated feeding of TCE or PCE to cultures after the change to anaerobic conditions yielded no further dechlorination. Only aerobic subcultures with an air/liquid ratio of 1:4 maintained dechlorination activities; anaerobic subcultures showed no transformation. Bacteria from noncontaminated sites showed no reduction under the same conditions. PMID:1892393

  19. 40 CFR Table 6 to Part 455 - PSES and PSNS for Priority Pollutants

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... 40 Protection of Environment 30 2011-07-01 2011-07-01 false PSES and PSNS for Priority Pollutants 6 Table 6 to Part 455 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) EFFLUENT... Pollutants Pollutant Daily maximum shall not exceed Monthly maximum shall not exceed 1,1-Dichloroethylene...

  20. FRACTIONATION OF STABLE CARBON ISOTOPES DURING ABIOTIC TRANSFORMATION OF TCE

    EPA Science Inventory

    At a Superfund Site in Minnesota, ground water is contaminated with trichloroethylene (TCE) with the contaminant plume stretching over five miles long. The ground water is iron and manganese reducing, and the complete absence of dichloroethylene, vinyl chloride, and ethene in th...

  1. 40 CFR Table 10 to Subpart Hhhhhhh... - HAP Subject to the Resin and Process Wastewater Provisions at New and Existing Sources

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... chloride VOC Method 107 at 40 CFR part 61, appendix B. 75354 Vinylidene chloride (1,1-Dichloroethylene) VOC SW-846-8260B.a 1330207 Xylenes (isomers and mixtures) VOC SW-846-8260B.a a Incorporated by...

  2. Polyaryl ethers and related polysiloxane copolymer molecular coatings preparation and radiation degrdation

    NASA Technical Reports Server (NTRS)

    Mcgrath, J. E.; Hedrick, J. L.; Webster, D. C.; Johnson, B. C.; Mohanty, D. K.; Yilgor, I.

    1983-01-01

    Poly(arylene ether sulfones) comprise a class of materials known as engineering thermoplastics which have a variety of important applications. These polymers are tough, rigid materials with good mechanical properties over a wide temperature range, and they are processed by conventional methods into products typically having excellent hydrolytic, thermal, oxidative and dimensional stability. Wholly aromatic random copolymers of hydroquinone and biphenol with 4.4 prime dichlorodiphenyl sulfone were synthesized via mechanical nucleophilic displacement. Their structures were characterized and mechanical behavior studied. These tough, ductile copolymers show excellent radiation resistance to electron beam treatment and retain much of the mechanical properties up to at least 700 Mrads under argon.

  3. Polyaryl ethers and related polysiloxane copolymer molecular coatings preparation and radiation degradation. Final report

    SciTech Connect

    Mcgrath, J.E.; Hedrick, J.L.; Webster, D.C.; Johnson, B.C.; Mohanty, D.K.; Yilgor, I.

    1983-06-01

    Poly(arylene ether sulfones) comprise a class of materials known as engineering thermoplastics which have a variety of important applications. These polymers are tough, rigid materials with good mechanical properties over a wide temperature range, and they are processed by conventional methods into products typically having excellent hydrolytic, thermal, oxidative and dimensional stability. Wholly aromatic random copolymers of hydroquinone and biphenol with 4.4 prime dichlorodiphenyl sulfone were synthesized via mechanical nucleophilic displacement. Their structures were characterized and mechanical behavior studied. These tough, ductile copolymers show excellent radiation resistance to electron beam treatment and retain much of the mechanical properties up to at least 700 Mrads under argon.

  4. Comparison of organochlorine residues in human adipose tissue autopsy samples from two Ontario municipalities

    SciTech Connect

    Williams, D.T.; LeBel, G.L.; Junkins, E.

    1984-01-01

    Human adipose tissue samples obtained during autopsies in a Canadian Great Lakes community, Kingston, Ontario, and a second community, Ottawa, Ontario, were analyzed for organochlorine pesticides, polychlorobiphenyls, chlorobenzenes, and chlorophenols. Significantly different levels of Dichlorodiphenyl-dichlorethane, mirex, hexachlorobenzene, and 2,3,4,6-tetrachlorophenol were found in Kingston adipose tissues compared to Ottawa tissues. Residue levels of oxychlordane, mirex, and polychlorinated biphenyls were significantly different in Kingston males versus Kingston females. The means and ranges of residue levels were contrasted with those reported in previous Canadian surveys.

  5. Induction of toluene oxidation activity in pseudomonas mendocina KR1 and pseudomonas sp. strain ENVPC5 by chlorinated solvents and alkanes

    SciTech Connect

    McClay, K.; Streger, S.H.; Steffan, R.J.

    1995-09-01

    Toluene oxidation activity in Pseudomonas mendocina KR1 and Pseudomonas sp. strain ENVPC5 was induced by trichloroethylene (TCE), and induction was followed by the degradation of TCE. Higher levels of toluene oxidation activity were achieved in the presence of a supplemental growth substrate such as glutamate, with levels of activity of up to 86% of that observed with toluene-induced cells. Activity in P. mendocina KR1 was also induced by cis-1,2-dichloroethylene, perchloroethylene, chloroethane, hexane, pentane, and octane, but not by trans-1,2-dichloroethylene. Toluene oxidation was not induced by TCE in Burkholderia (Pseudomonas) cepacia G4, P. putida F1, Pseudomonas sp. strain ENV110, or Pseudomonas sp. strain ENV113. 22 refs., 4 tabs.

  6. Interim sanitary landfill groundwater monitoring report. 1995 annual report

    SciTech Connect

    Bagwell, L.

    1996-04-24

    Eight wells of the LFW series monitor groundwater quality in the Steed Pond Aquifer (Water Table) beneath the Interim Sanitary Landfill at the Savannah River Site (SRS). These wells are sampled biannually to comply with the South Carolina Department of Health and Environmental Control Modified Municipal Solid Waste Permit 025500- 1120 (formerly DWP-087A) and as part of the SRS Groundwater Monitoring Program. Trichlorofluoromethane was elevated in one downgradient and one sidegradient well during 1995. Barium, 1, 1- dichloroethylene, specific conductance, and zinc exceeded standards in one well each. The elevated level of 1, 1-dichloroethylene occurred in a downgradient well. The groundwater flow direction in the Steed Pond Aquifer (Water Table) beneath the Sanitary Landfill was to the southeast (universal transverse Mercator coordinates). The flow rate in this unit was approximately 190 ft/year during first quarter 1995 and 150 ft/yr during third quarter 1995.

  7. Health assessment for Keystone Hydraulics/J. W. Rex Company, Lansdale, Pennsylvania, Region 3. CERCLIS No. PAD980926976. Preliminary report

    SciTech Connect

    Not Available

    1988-05-04

    The Keystone Hydraulics/J. W. Rex Company Site has been listed on the National Priorities List. A metal heat-treating facility operated there from the 1940s until 1950. The Allied Paint Company then conducted operations until 1979. The site has been a construction equipment storage area since 1979. Identified contaminants of concern on-site include trichloroethylene (TCE), perchloroethylene (PCE), 1,1-dichloroethylene (1,1-DCE), cis-1,2-dichloroethylene (DCE), and vinyl chloride in well water. Identified soil contaminants include DCE, TCE, PCE, and vinyl chloride. Off-site contamination of groundwater by TCE and vinyl chloride has been found. The site is considered to be of potential public health concern because of the risk to human health caused by the possibility of exposure to hazardous substances via groundwater and soil.

  8. Evaluation of HCFC AK 225 Alternatives for Precision Cleaning and Verification

    NASA Technical Reports Server (NTRS)

    Melton, D. M.

    1998-01-01

    Maintaining qualified cleaning and verification processes are essential in an production environment. Environmental regulations have and are continuing to impact cleaning and verification processing in component and large structures, both at the Michoud Assembly Facility and component suppliers. The goal of the effort was to assure that the cleaning and verification proceeds unimpeded and that qualified, environmentally compliant material and process replacements are implemented and perform to specifications. The approach consisted of (1) selection of a Supersonic Gas-Liquid Cleaning System; (2) selection and evaluation of three cleaning and verification solvents as candidate alternatives to HCFC 225 (Vertrel 423 (HCFC), Vertrel MCA (HFC/1,2-Dichloroethylene), and HFE 7100DE (HFE/1,2 Dichloroethylene)); and evaluation of an analytical instrumental post cleaning verification technique. This document is presented in viewgraph format.

  9. Sphingomonas taxi, Isolated from Cucurbita pepo, Proves to Be a DDE-Degrading and Plant Growth-Promoting Strain.

    PubMed

    Eevers, Nele; Van Hamme, Jonathan D; Bottos, Eric M; Weyens, Nele; Vangronsveld, Jaco

    2015-01-01

    The draft genome of Sphingomonas taxi, a strain of the Sphingomonadaceae isolated from Cucurbita pepo root tissue, is presented. This Gram-negative bacterium shows 2,2-bis(p-chlorophenyl)-1,1-dichloroethylene (DDE)-degrading potential and plant growth-promoting capacities. An analysis of its 3.9-Mb draft genome will enhance the understanding of DDE-degradation pathways and phytoremediation applications for DDE-contaminated soils. PMID:25977415

  10. Laboratory Evaluation of Drop-in Solvent Alternatives to n-Propyl Bromide for Vapor Degreasing

    NASA Technical Reports Server (NTRS)

    Mitchell, Mark A.; Lowrey, Nikki M.

    2012-01-01

    Based on this limited laboratory study, solvent blends of trans-1,2 dichloroethylene with HFEs, HFCs, or PFCs appear to be viable alternatives to n-propyl bromide for vapor degreasing. The lower boiling points of these blends may lead to greater solvent loss during use. Additional factors must be considered when selecting a solvent substitute, including stability over time, VOC, GWP, toxicity, and business considerations.

  11. Draft Genome Sequence of Methylobacterium radiotolerans, a DDE-Degrading and Plant Growth-Promoting Strain Isolated from Cucurbita pepo

    PubMed Central

    Eevers, Nele; Van Hamme, Jonathan D.; Bottos, Eric M.; Weyens, Nele

    2015-01-01

    We announce the draft genome of Methylobacterium radiotolerans, a Gram-negative bacterium isolated from Cucurbita pepo roots. This strain shows 2,2-bis(p-chlorophenyl)-1,1-dichloroethylene (DDE)-degrading potential and plant growth-promoting capacities. Analyses of its 6.8-Mb genome will improve our understanding of DDE-degradation pathways and aid in the deployment of phytoremediation technologies to remediate DDE-contaminated soils. PMID:25977414

  12. Sphingomonas taxi, Isolated from Cucurbita pepo, Proves to Be a DDE-Degrading and Plant Growth-Promoting Strain

    PubMed Central

    Eevers, Nele; Van Hamme, Jonathan D.; Bottos, Eric M.; Weyens, Nele

    2015-01-01

    The draft genome of Sphingomonas taxi, a strain of the Sphingomonadaceae isolated from Cucurbita pepo root tissue, is presented. This Gram-negative bacterium shows 2,2-bis(p-chlorophenyl)-1,1-dichloroethylene (DDE)-degrading potential and plant growth-promoting capacities. An analysis of its 3.9-Mb draft genome will enhance the understanding of DDE-degradation pathways and phytoremediation applications for DDE-contaminated soils. PMID:25977415

  13. Draft Genome Sequence of Enterobacter aerogenes, a DDE-Degrading and Plant Growth-Promoting Strain Isolated from Cucurbita pepo

    PubMed Central

    Eevers, Nele; Van Hamme, Jonathan D.; Bottos, Eric M.; Weyens, Nele

    2015-01-01

    We report here the draft genome of Enterobacter aerogenes, a Gram-negative bacterium of the Enterobacteriaceae isolated from Cucurbita pepo root tissue. This bacterium shows 2,2-bis(p-chlorophenyl)-1,1-dichloroethylene (DDE)-degrading potential and plant growth-promoting capacity. An analysis of its 4.5-Mb draft genome will enhance the understanding of DDE degradation pathways and phytoremediation applications for DDE-contaminated soils. PMID:25883299

  14. 40 CFR 141.61 - Maximum contaminant levels for organic contaminants.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ...-Dichloroethylene 0.07 (10) 78-87-5 1,2-Dichloropropane 0.005 (11) 100-41-4 Ethylbenzene 0.7 (12) 108-90-7... Endrin X 100-41-4 Ethylbenzene X X 106-93-4 Ethylene Dibromide (EDB) X X 1071-83-6 Gylphosate X 76-44-8... X 58-89-9 Lindane X 72-43-5 Methoxychlor X 108-90-7 Monochlorobenzene X X 23135-22-0 Oxamyl...

  15. 40 CFR 141.61 - Maximum contaminant levels for organic contaminants.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ...-Dichloroethylene 0.07 (10) 78-87-5 1,2-Dichloropropane 0.005 (11) 100-41-4 Ethylbenzene 0.7 (12) 108-90-7... Endrin X 100-41-4 Ethylbenzene X X 106-93-4 Ethylene Dibromide (EDB) X X 1071-83-6 Gylphosate X 76-44-8... X 58-89-9 Lindane X 72-43-5 Methoxychlor X 108-90-7 Monochlorobenzene X X 23135-22-0 Oxamyl...

  16. 40 CFR 141.61 - Maximum contaminant levels for organic contaminants.

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ...-Dichloroethylene 0.07 (10) 78-87-5 1,2-Dichloropropane 0.005 (11) 100-41-4 Ethylbenzene 0.7 (12) 108-90-7... Endrin X 100-41-4 Ethylbenzene X X 106-93-4 Ethylene Dibromide (EDB) X X 1071-83-6 Gylphosate X 76-44-8... X 58-89-9 Lindane X 72-43-5 Methoxychlor X 108-90-7 Monochlorobenzene X X 23135-22-0 Oxamyl...

  17. 40 CFR 141.61 - Maximum contaminant levels for organic contaminants.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ...-Dichloroethylene 0.07 (10) 78-87-5 1,2-Dichloropropane 0.005 (11) 100-41-4 Ethylbenzene 0.7 (12) 108-90-7... Endrin X 100-41-4 Ethylbenzene X X 106-93-4 Ethylene Dibromide (EDB) X X 1071-83-6 Gylphosate X 76-44-8... X 58-89-9 Lindane X 72-43-5 Methoxychlor X 108-90-7 Monochlorobenzene X X 23135-22-0 Oxamyl...

  18. 40 CFR 141.61 - Maximum contaminant levels for organic contaminants.

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ...-Dichloroethylene 0.07 (10) 78-87-5 1,2-Dichloropropane 0.005 (11) 100-41-4 Ethylbenzene 0.7 (12) 108-90-7... Endrin X 100-41-4 Ethylbenzene X X 106-93-4 Ethylene Dibromide (EDB) X X 1071-83-6 Gylphosate X 76-44-8... X 58-89-9 Lindane X 72-43-5 Methoxychlor X 108-90-7 Monochlorobenzene X X 23135-22-0 Oxamyl...

  19. High-harmonic spectroscopy of molecular isomers

    SciTech Connect

    Wong, M. C. H.; Brichta, J.-P.; Bhardwaj, V. R.; Spanner, M.; Patchkovskii, S.

    2011-11-15

    We demonstrate that high-order-harmonic generation (HHG) spectroscopy can be used to probe stereoisomers of randomly oriented 1,2-dichloroethylene (C{sub 2}H{sub 2}Cl{sub 2}) and 2-butene (C{sub 4}H{sub 8}). The high-harmonic spectra of these isomers are distinguishable over a range of laser intensities and wavelengths. Time-dependent numerical calculations of angle-dependent ionization yields for 1,2-dichloroethylene suggest that the harmonic spectra of molecular isomers reflect differences in their strong-field ionization. The subcycle ionization yields for the cis isomer are an order of magnitude higher than those for the trans isomer. The sensitivity in discrimination of the harmonic spectra of cis- and trans- isomers is greater than 8 and 5 for 1,2-dichloroethylene and 2-butene, respectively. We show that HHG spectroscopy cannot differentiate the harmonic spectra of the two enantiomers of the chiral molecule propylene oxide (C{sub 3}H{sub 6}O).

  20. Halocarbons in the environment: Estimates of thermodynamic properties for aqueous chloroethylene species and their stabilities in natural settings

    SciTech Connect

    Haas, J.R.; Shock, E.L.

    1999-10-01

    Standard partial molal thermodynamic parameters for the aqueous chlorinated-ethylene species, perchloroethylene (PCE), trichloroethylene (TCE), 1,1-dichloroethylene (1,1-DCE), cis-1,2-dichloroethylene (cis-1,2-DCE), trans-1,2-dichloroethylene (trans-1,2-DCE), and vinyl chloride (VC) have been estimated by using experimental gas-solubility data and correlation algorithms. The provided thermodynamic values may be used to calculate properties of reactions involving the aqueous chloroethylene species at a wide range of temperatures and pressures. Estimated values for the chloroethylenes were used, along with published values for minerals, gases, aqueous ions, and aqueous neutral organic species, to calculate the stability of chloroethylene species in equilibrium with the minerals magnetite, hematite, pyrite, and pyrrhotite in the subsurface. Estimated values for the aqueous chloroethylenes were also used to calculate reduction potentials for microbially-mediated reductive dechlorination half-reactions at elevated temperatures. Calculations indicate that all aqueous chloroethylene species are energetically favored to decompose to ethylene(aq) under a wide range of conditions in the subsurface, by both abiotic and biotic pathways. Anaerobic microbially mediated degradation is especially favored under conditions at least sufficiently reducing to promote sulfate-reduction, but not under conditions sufficient for microbial denitrification, pyrolusite reduction, or ferric-iron reduction.

  1. Halocarbons in the environment: estimates of thermodynamic properties for aqueous chloroethylene species and their stabilities in natural settings

    NASA Astrophysics Data System (ADS)

    Haas, Johnson R.; Shock, Everett L.

    1999-10-01

    Standard partial molal thermodynamic parameters for the aqueous chlorinated-ethylene species, perchloroethylene (PCE), trichloroethylene (TCE), 1,1-dichloroethylene (1,1-DCE), cis-1,2-dichloroethylene (cis-1,2-DCE), trans-1,2-dichloroethylene (trans-1,2,-DCE), and vinyl chloride (VC) have been estimated by using experimental gas-solubility data and correlation algorithms. The provided thermodynamic values may be used to calculate properties of reactions involving the aqueous chloroethylene species at a wide range of temperatures and pressures. Estimated values for the chloroethylenes were used, along with published values for minerals, gases, aqueous ions, and aqueous neutral organic species, to calculate the stability of chloroethylene species in equilibrium with the minerals magnetite, hematite, pyrite, and pyrrhotite in the subsurface. Estimated values for the aqueous chloroethylenes were also used to calculate reduction potentials for microbially-mediated reductive dechlorination half-reactions at elevated temperatures. Calculations indicate that all aqueous chloroethylene species are energetically favored to decompose to ethylene(aq) under a wide range of conditions in the subsurface, by both abiotic and biotic pathways. Anaerobic microbially mediated degradation is especially favored under conditions at least sufficiently reducing to promote sulfate-reduction, but not under conditions sufficient for microbial denitrification, pyrolusite reduction, or ferric-iron reduction.

  2. Superfund Record of Decision (EPA Region 2): Gloucester Environmental Management Services (GEMS) Landfill, Gloucester Township, Camden County, New Jersey, September 1985. Final report

    SciTech Connect

    Not Available

    1985-09-27

    The 60-acre GEMS Landfill site is located in Gloucester Township, New Jersey. Gloucester Township has owned the GEMS site from the late 1950's up to the present. During the time period the GEMS Landfill has been operated by various parties as a disposal site for solid, liquid, and hazardous wastes and substances. Records indicate that a variety of industrial wastes including asbestos, solvents and other materials were disposed of at the GEMS site between 1970 and 1979. In 1980, sludge from the City of Philadelphia's northeast wastewater treatment facility was disposed of at GEMS. Analyses of the sludge revealed the presence of dichlorodiphenyl dichloroethane (DDD). The results of the RI show that ground water, surface water (Holly Run) and soil are severely contaminated with organic and inorganic hazardous substances. Also, volatile organic compounds are volatilizing into the atmosphere and significantly degrading air quality.

  3. Breastmilk contaminants and infant behavior

    SciTech Connect

    Worobey, J.; Thomas, D.A.; Lewis, M. )

    1990-02-26

    Recent work has shown that certain heavy metals, polychlorinated biphenyls (PCBs), and dichlorodiphenyl dichloroethene (p,p{prime}-DDE) can affect newborn behavior via transplacental exposure. In this study, a number of fluids were collected from a sample of mothers and infants, with gas liquid chromatography used to determine the levels of environmental contaminants in breastmilk obtained in the first postpartum week. Analysis of the first 15 cases revealed normal concentrations of metals, no detectable traces of PCBs, and detectable levels of heptachlor epoxide and p,p{prime}-DDE in breastmilk. No significant associations were found between metals and infant development, but p,p{prime}-DDE was inversely related to perceptual performance and motor scores at 2-1/2 years. These results suggest that contaminants in human milk may affect infant behavior beyond the newborn period, although prediction from other sources must also be considered.

  4. Monitoring of a wide range of organic micropollutants on the Portuguese coast using plastic resin pellets.

    PubMed

    Mizukawa, Kaoruko; Takada, Hideshige; Ito, Maki; Geok, Yeo Bee; Hosoda, Junki; Yamashita, Rei; Saha, Mahua; Suzuki, Satoru; Miguez, Carlos; Frias, João; Antunes, Joana Cepeda; Sobral, Paula; Santos, Isabelina; Micaelo, Cristina; Ferreira, Ana Maria

    2013-05-15

    We analyzed polychlorinated biphenyls (PCBs), dichlorodiphenyl dichloroethane and its metabolites, hexachlorocyclohexanes (HCHs), polycyclic aromatic hydrocarbons (PAHs), and hopanes, in plastic resin pellets collected from nine locations along the Portuguese coast. Concentrations of a sum of 13 PCBs were one order of magnitude higher in two major cities (Porto: 307 ng/g-pellet; Lisboa: 273 ng/g-pellet) than in the seven rural sites. Lower chlorinated congeners were more abundant in the rural sites than in the cities, suggesting atmospheric dispersion. At most of the locations, PAH concentrations (sum of 33 PAH species) were ∼100 to ∼300 ng/g-pellet; however, three orders of magnitude higher concentrations of PAHs, with a petrogenic signature, were detected at a small city (Sines). Hopanes were detected in the pellets at all locations. This study demonstrated that multiple sample locations, including locations in both urban and remote areas, are necessary for country-scale pellet watch. PMID:23499535

  5. Persistent Organic Pollutants in albacore tuna (Thunnus alalunga) from Reunion Island (Southwest Indian Ocean) and South Africa in relation to biological and trophic characteristics.

    PubMed

    Munschy, C; Bodin, N; Potier, M; Héas-Moisan, K; Pollono, C; Degroote, M; West, W; Hollanda, S J; Puech, A; Bourjea, J; Nikolic, N

    2016-07-01

    The contamination of albacore tuna (Thunnus alalunga) by Persistent Organic Pollutants (POPs), namely polychlorinated biphenyls (PCBs) and dichlorodiphenyl-trichloroethane (DDT), was investigated in individuals collected from Reunion Island (RI) and South Africa's (SA) southern coastlines in 2013, in relation to biological parameters and feeding ecology. The results showed lower PCB and DDT concentrations than those previously reported in various tuna species worldwide. A predominance of DDTs over PCBs was revealed, reflecting continuing inputs of DDT. Tuna collected from SA exhibited higher contamination levels than those from RI, related to higher dietary inputs and higher total lipid content. Greater variability in contamination levels and profiles was identified in tuna from RI, explained by a higher diversity of prey and more individualistic foraging behaviour. PCB and DDT contamination levels and profiles varied significantly in tuna from the two investigated areas, probably reflecting exposure to different sources of contamination. PMID:27084988

  6. Serum PCB and DDE levels of frequent Great Lakes sport fish consumers -- A first look

    SciTech Connect

    Hanrahan, L.P.; Falk, C.; Anderson, H.A.; Draheim, L.; Olson, J.; Kanarek, M.S.

    1999-02-01

    Great Lakes (GL) sport fish consumption is a potential human exposure route for polychlorinated biphenyls (PCBs) and dichlorodiphenyl dichloroethene (DDE). Because of fish tissue contamination, frequent consumers of Great Lakes sport caught fish (GLSCF) may be at risk for PCB and DDE accumulation. To examine this problem, the Health Departments of Wisconsin, Illinois, Indiana, Ohio, and Michigan formed a health assessment consortium. Participants were contacted by telephone to complete a detailed demographic and fish consumption survey. Frequent and infrequent GLSCF consumers were identified, and a participant subset was then asked to donate blood for PCB and DDE analysis. Analysis of variance (ANOVA) was done to study exposure group mean differences, while correlation and regression analyses were performed to examine relationships between demographic characteristics, GLSCF consumption, PCB, and DDE body burdens.

  7. Limited site investigation of Landfills 1 and 4, Fort Lewis, Washington

    SciTech Connect

    Last, G.V.; Eddy, P.A.; Airhart, S.P.; Olsen, K.R.; Raymond, J.R.; Dahl, D.R.

    1990-08-01

    The information presented in this report was collected during limited site investigation activities conducted in the vicinity of Landfills 1 and 4 at Fort Lewis. The purpose of this work was to provide a means of detecting and evaluating the impacts of these inactive landfills on ground-water quality and adjacent lands. This effort included the design and construction of ground-water monitoring systems for compliance with applicable federal and state regulations governing Resource Conservation and Recovery Act (RCRA)-type landfills. Ground-water samples were collected from both existing (1981 and 1984) wells and the newly installed (1988) wells. The analytical results from the water samples indicate that the ground water in and around Landfill 1 contains limited contamination. Contaminants may include volatile organic compounds and nitrate. The primary concern in the area around Landfill 1 was the determination that ground water from two wells may contain cis-1,2-dichloroethylene and 1,1,1-trichloroethylene above drinking water standards. Nitrate levels in the downgradient wells were greater than those in upgradient wells and exceeded drinking water standards in some of the less-representative samples. Analyses of ground-water samples from wells in and around Landfill 4 indicate several contaminants may be present. These include volatile organic compounds (principally cis-1,2-dichloroethylene and 1,1,1-trichloroethylene), coliform, oil and grease, and perhaps some metals (iron and magnesium). The primary concern in the area around Landfill 4 was the determination that ground water from five wells contained cis-1,2-dichloroethylene and 1,1,1-trichloroethylene above drinking water standards. The source of contaminants beneath either landfill cannot yet be identified. Insufficient data exist to disprove or confirm either landfill as possible contributors. 19 refs., 32 figs., 17 tabs.

  8. Transformation yields of chlorinated ethenes by a methanotrophic mixed culture expressing particulate methane monooxygenase.

    PubMed Central

    Anderson, J E; McCarty, P L

    1997-01-01

    Transformation yields for the aerobic cometabolic degradation of five chlorinated ethenes were determined by using a methanotrophic mixed culture expressing particulate methane monooxygenase (pMMO). Transformation yields (expressed as moles of chlorinated ethene degraded per mole of methane consumed) were 0.57, 0.25, 0.058, 0.0019, and 0.00022 for trans-1,2-dichloroethylene (t-DCE), vinyl chloride (VC), cis-1,2-dichloroethylene (c-DCE), trichloroethylene (TCE), and 1,1-dichloroethylene (1,1-DCE), respectively. Degradation of t-DCE and VC was observed only in the presence of formate or methane, sources of reducing energy necessary for cometabolism. The t-DCE and VC transformation yields represented 35 and 15%, respectively, of the theoretical maximum yields, based on reducing-energy availability from methane dissimilation to carbon dioxide, exclusive of all other processes that require reducing energy. The yields for t-DCE and VC were 20 times greater than the yields reported by others for cells expressing soluble methane monooxygenase (sMMO). Transformation yields for c-DCE, TCE, and 1,1-DCE were similar to or less than those for cultures expressing sMMO. Although methanotrophic biotreatment systems have typically been designed to incorporate cultures expressing sMMO, these results suggest that pMMO expression may be highly advantageous for degradation of t-DCE or VC. It may also be much easier to maintain pMMO expression in treatment systems, because pMMO is expressed by all methanotrophs whereas sMMO is expressed only by type II methanotrophs under copper-limited conditions. PMID:9023946

  9. Quarterly sampling of the wetlands along the old F-Area effluent ditch: March 1994

    SciTech Connect

    Dixon, K.L.; Cummins, C.L.; Rogers, V.A.

    1994-05-01

    In March 1994, well point water and near surface water (bucket) samples were collected to further characterize tritium and volatile organic compounds (VOC) in the wetlands along the old F-Area effluent ditch south of 643-E (old burial ground). Groundwater flow paths suggest that compounds detected in water table wells around 643-E would migrate towards the old F-Area effluent ditch and Fourmile Branch. Recent analytical results from near surface water sampling in the wetlands that comprise the old F-Area effluent ditch have shown that tritium and small quantities of VOCs are outcropping in the area. Results of the March 1994 sampling event further support findings that tritium and volatile organic compounds originating from 643-E are outcropping in the wetlands near the old F-Area effluent ditch. Six different analytes were detected in the well points at least once at concentrations greater than the method detection limit: d 1,2-dichloroethylene, acetone, methyl ethyl ketone, tetrachloroethylene, trichloroethylene, and tritium. 1,2-dichloroethylene, tetrachloroethylene, trichloroethylene, and tritium were detected at levels above Primary Drinking Water Standards or Maximum Contaminant Levels list. Four analytes, 1,2-dichloroethylene, trichloroethylene, tritium, and vinyl chloride, were detected at least once at concentrations greater than the method detection limit and least once at concentrations above the PDWS or the MCL. Based on differences in tritium concentrations at each location, it was determined that the sampling devices intercepted different groundwater flow paths. This negated direct comparison of analytical results between devices. However, when VOC concentrations measured at each well point and bucket location were normalized, resulting well point and bucket VOC concentrations were comparable in most cases. These results suggest that volatilization losses of VOCs from the buckets were negligible.

  10. Resonant inelastic x-ray scattering on iso-C{sub 2}H{sub 2}Cl{sub 2} around the chlorine K-edge: Structural and dynamical aspects

    SciTech Connect

    Kawerk, Elie E-mail: ekawerk@units.it; Carniato, Stéphane; Journel, Loïc; Marchenko, Tatiana; Simon, Marc; Piancastelli, Maria Novella; Žitnik, Matjaž; Bučar, Klemen; Bohnic, Rok; and others

    2014-10-14

    We report a theoretical and experimental study of the high resolution resonant K{sub α} X-ray emission lines around the chlorine K-edge in gas phase 1,1-dichloroethylene. With the help of ab initio electronic structure calculations and cross section evaluation, we interpret the lowest lying peak in the X-ray absorption and emission spectra. The behavior of the K{sub α} emission lines with respect to frequency detuning highlights the existence of femtosecond nuclear dynamics on the dissociative Potential Energy Surface of the first K-shell core-excited state.

  11. Decomposition of chlorinated ethylenes and ethanes in an electron beam generated plasma reactor

    SciTech Connect

    Vitale, S.A.

    1996-02-01

    An electron beam generated plasma reactor (EBGPR) is used to determine the plasma chemistry kinetics, energetics and decomposition pathways of six chlorinated ethylenes and ethanes: 1,1,1-trichloroethane, 1,1-dichloroethane, ethyl chloride, trichloroethylene, 1,1-dichloroethylene, and vinyl chloride. A traditional chemical kinetic and chemical engineering analysis of the data from the EBGPR is performed, and the following hypothesis was verified: The specific energy required for chlorinated VOC decomposition in the electron beam generated plasma reactor is determined by the electron attachment coefficient of the VOC and the susceptibility of the molecule to radical attack. The technology was demonstrated at the Hanford Reservation to remove VOCs from soils.

  12. Emerging technology summary: Destruction of organic contaminants in air using advanced ultraviolet flashlamps

    SciTech Connect

    Not Available

    1993-07-01

    The summary describes a new process for photo-oxidation of volatile organic compounds (VOCs) in air using an advanced ultraviolet (UV) source, and a pulsed xenon flashlamp. The flashlamps have greater output at 200 to 250 nm than medium-pressure mercury lamps at the same power and, therefore, cause much more rapid direct photolysis of VOCs. The observation of quantum yields greater than unity indicate the involvement of chain reactions for trichloroethene (TCE), perchloroethene (PCE), 1,1-dichloroethylene (DCE), CHCl3, and CH2Cl2. TCE was examined more closely because of its widespread occurrence and very high destruction rate.

  13. Biodegradation and biotransformation of groundwater pollutant mixtures by mycobacterium vaccae

    SciTech Connect

    Burback, B.L.; Perry, J.J. )

    1993-04-01

    This study examines the catabolic activity of Mycobacterium vaccae in regard to 11 ground water pollutants and effect of intermediates on the catabolism of these pollutants and the degradative abilities of the bacteria. The pollutants were tested singly and in mixtures and included the following: acetone, toluene, propylbenzene, 1,2-dichloroethylene, o-xylene, dioxane, styrene, cyclohexane, benzene, ethylbenzene, chlorobenzene. The results indicate that M. vaccae can catabolize all 11 ground water pollutants to more water-soluable compounds, with only acetone and toluene supporting growth. 26 refs., 5 figs.

  14. Mineralization of trichloroethylene by heterotrophic enrichment cultures

    SciTech Connect

    Phelps, T.J.; Ringelberg, D.; Mikell, A.T.; White, D.C. |; Fliermans, C.B.

    1988-12-31

    Microbial consortia capable of aerobically degrading greater than 99% of 50 mg/l exogenous trichloroethylene (TCE) have been enriched from TCE contaminated subsurface sediments. Concentrations of TCE greater than 300 mg/l were not degraded nor was TCE used as a sole energy source. Successful electron donors for growth included tryptone-yeast extract, methanol, methane or propane. The optimum temperature for growth was 22--37 C and the ph optimum was 7.0--8.1. Utilization of TCE occurred only after apparent microbial growth had ceased. The major end products recovered were hydrochloric acid and carbon dioxide. Minor products included dichloroethylene, vinylidine chloride and possibly chloroform.

  15. Mixed Waste Management Facility (MWMF) groundwater monitoring report. Second quarter 1993

    SciTech Connect

    Not Available

    1993-09-01

    Groundwater monitoring continued at the Savannah River Plant. During second quarter 1993, nine constituents exceeded final Primary Drinking Water Standards in groundwater samples from downgradient monitoring wells at the Mixed Waste Management Facility, the Old Burial Ground, the E-Area Vaults, and the proposed Hazardous Waste/Mixed Waste Disposal Vaults. As in previous quarters, tritium and trichloroethylene were the most widespread constituents. Chloroethene (vinyl chloride), dichloromethane (methylene chloride), 1,1-dichloroethylene, gross alpha, lead, nonvolatile beta, or tetrachloroethylene also exceeded standards in one or more wells. The groundwater flow directions and rates in the three hydrostratigraphic units were similar to those of previous quarters.

  16. Health assessment for Watkins-Johnson Facility, Scotts Valley, California, Region 9. CERCLIS No. CAD980893234. Preliminary report

    SciTech Connect

    Not Available

    1988-06-30

    The Watkins-Johnson facility is on the National Priorities List. The facility manufactures electronic components. The environmental sampling conducted to date indicates that the contaminants of concern at the site are predominantly VOCs present in ground water, surface water, and soil. The VOCs present in one or more environmental media include trichloroethylene (TCE); 1,2-dichloroethylene (DCE); tetrachloroethylene perchloroethylene (PCE); vinyl chloride; methylene chloride; 1,1,1-trichloroethane (TCA); and Freon 113. The site is considered to be of potential public health concern because of the risk to human health caused by the possibility of exposure to hazardous substances via ingestion of contaminated ground water.

  17. Investigation of ground-water pollution at Air Force Plant Number 4, Fort Worth Texas

    SciTech Connect

    Not Available

    1986-10-01

    Beginning in December 1982, an extensive investigation was conducted to determine the presence and extent of industrial chemical pollution at Air Force Plant No. 4. A major portion of this work was devoted to the testing of ground water flowing within the overburden. In addition, 16 wells were drilled to monitor for polluted ground water in the upper and middle zones of the Paluxy Formation. Paluxy ground water was monitored; trichloroethylene, 1,2-trans-dichloroethylene, and lesser amounts of other chlorinated hydrocarbons, and the existence of abnormally high water levels in the upper zone of the Paluxy Formation in well P-8(U) were discovered.

  18. Superfund Record of Decision (EPA Region 7): Des Moines TCE Site, Operable Unit 3, Des Moines, IA. (Second remedial action), September 1992. Final report

    SciTech Connect

    Not Available

    1992-09-18

    The Des Moines TCE site is located southwest of downtown Des Moines, Polk County, Iowa. Land use in the area is predominantly industrial and commercial, and part of the site lies within the floodplain of the Raccoon River. Water from the Des Moines Water Works north infiltration gallery was found to be contaminated with trichloroethylene (TCE), dichloroethylene (DCE), and vinyl chloride at levels above accepted drinking water standards. The ROD addresses OU3, which encompasses potential sources of ground water contamination in an area north of the Raccoon River. The selected remedial action for OU3 includes no action with periodic groundwater monitoring.

  19. Superfund Record of Decision (EPA region 2): Brewster Well Field, Brewster, Putnam County, New York, September 1986. Final report

    SciTech Connect

    Not Available

    1986-09-30

    The Brewster Well Field, located on the northern bank of the East Branch Croton River, is three-quarters of a mile east of the Village of Brewster, Town of Southeast, Putnam County, NY. Since 1954 when Well Field No. 1 was developed, the Village of Brewster has used the aquifers beneath the Village-owned land as a water supply source. In 1967 Well Field No. 2 was brought on line. In 1978 evidence of volatile halogenated organic compound contamination from an unidentified source first appeared. VHOs have been the primary contaminants detected in the ground water. The principal contaminants were found to be tetrachloroethylene, trichloroethylene, and 1,2-dichloroethylene.

  20. 40 CFR Table 1 to Subpart Dd of... - List of Hazardous Air Pollutants (HAP) for Subpart DD

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... Benzotrichloride (isomers and mixture) 0.958 100-44-7 Benzyl chloride 1.000 92-52-4 Biphenyl 0.864 542-88-1 Bis... 0.499 110-54-3 Hexane 1.000 78-59-1 Isophorone 0.506 58-89-9 Lindane (all isomers) 1.000 67-56-1...-Dichloroethylene) 1.000 1330-20-7 Xylenes (isomers and mixture) 1.000 95-47-6 o-Xylenes 1.000 108-38-3 m-Xylenes...

  1. 40 CFR Table 1 to Subpart Dd of... - List of Hazardous Air Pollutants (HAP) for Subpart DD

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... Benzotrichloride (isomers and mixture) 0.958 100-44-7 Benzyl chloride 1.000 92-52-4 Biphenyl 0.864 542-88-1 Bis... 0.499 110-54-3 Hexane 1.000 78-59-1 Isophorone 0.506 58-89-9 Lindane (all isomers) 1.000 67-56-1...-Dichloroethylene) 1.000 1330-20-7 Xylenes (isomers and mixture) 1.000 95-47-6 o-Xylenes 1.000 108-38-3 m-Xylenes...

  2. 40 CFR Table 1 to Subpart Dd of... - List of Hazardous Air Pollutants (HAP) for Subpart DD

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... Benzotrichloride (isomers and mixture) 0.958 100-44-7 Benzyl chloride 1.000 92-52-4 Biphenyl 0.864 542-88-1 Bis... 0.499 110-54-3 Hexane 1.000 78-59-1 Isophorone 0.506 58-89-9 Lindane (all isomers) 1.000 67-56-1...-Dichloroethylene) 1.000 1330-20-7 Xylenes (isomers and mixture) 1.000 95-47-6 o-Xylenes 1.000 108-38-3 m-Xylenes...

  3. 40 CFR Table 1 to Subpart Dd of... - List of Hazardous Air Pollutants (HAP) for Subpart DD

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... Benzotrichloride (isomers and mixture) 0.958 100-44-7 Benzyl chloride 1.000 92-52-4 Biphenyl 0.864 542-88-1 Bis... 0.499 110-54-3 Hexane 1.000 78-59-1 Isophorone 0.506 58-89-9 Lindane (all isomers) 1.000 67-56-1...-Dichloroethylene) 1.000 1330-20-7 Xylenes (isomers and mixture) 1.000 95-47-6 o-Xylenes 1.000 108-38-3 m-Xylenes...

  4. 40 CFR Table 1 to Subpart Dd of... - List of Hazardous Air Pollutants (HAP) for Subpart DD

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... Benzotrichloride (isomers and mixture) 0.958 100-44-7 Benzyl chloride 1.000 92-52-4 Biphenyl 0.864 542-88-1 Bis... 0.499 110-54-3 Hexane 1.000 78-59-1 Isophorone 0.506 58-89-9 Lindane (all isomers) 1.000 67-56-1...-Dichloroethylene) 1.000 1330-20-7 Xylenes (isomers and mixture) 1.000 95-47-6 o-Xylenes 1.000 108-38-3 m-Xylenes...

  5. Mixed Waste Management Facility (MWMF) groundwater monitoring report. Fourth quarter 1992 and 1992 summary

    SciTech Connect

    Not Available

    1993-03-01

    During fourth quarter 1992, nine constituents exceeded final Primary Drinking Water Standards (PDWS) in one or more groundwater samples from monitoring wells at the Mixed Waste Management Facility (MWMF) and adjacent facilities. As in previous quarters, tritium and trichloroethylene were the most widespread constituents. Fifty-seven (48%) of the 120 monitoring wells, contained elevated tritium activities, and 23 (19%) contained elevated trichloroethylene concentrations. Total alpha-emitting radium, tetrachloroethylene, chloroethene, cadmium, 1,1-dichloroethylene, lead, or nonvolatile beta levels exceeded standards in one or more wells. During 1992, elevated levels of 13 constituents were found in one or more of 80 of the 120 groundwater monitoring wells (67%) at the MWMF and adjacent facilities. Tritium and trichloroethylene exceeded their final PDWS more frequently and more consistently than did other constituents. Tritium activity exceeded its final PDWS m 67 wells and trichloroethylene was. elevated in 28 wells. Lead, tetrachloroethylene, total alpha-emitting radium, gross alpha, cadmium, chloroethene, 1,1-dichloroethylene 1,2-dichloroethane, mercury, or nitrate exceeded standards in one or more wells during the year. Nonvolatile beta exceeded its drinking water screening level in 3 wells during the year.

  6. Health assessment for Chemplex Company, Clinton, Clinton County, Iowa, Region 7. CERCLIS No. IAD045372836. Final report

    SciTech Connect

    Not Available

    1991-01-03

    The Chemplex Company site is a proposed National Priorities List (NPL) site situated approximately 2 miles northwest of Camanche and approximately 4 miles southwest of downtown Clinton in Clinton County, Iowa. On-site soils and on-site and off-site groundwater are contaminated with considerable amounts of volatile organic compounds (VOCs), i.e. benzene, 1,1-dichloroethylene, 1,2-dichloroethylene, trichloroethylene, xylene, toluene, ethylbenzene, etc., and polycyclic aromatic hydrocarbons (PAHs) at levels of public health concern. The populations at risk of exposure include employees at the facility, remedial and construction workers, and residents in close proximity to the site. There are approximately 475 employees at the facility. Ten residences having an estimated population of 25 persons are located at various locations within a half-mile radius of the site. Area residents utilize private wells to obtain groundwater from the shallow bedrock aquifer for domestic and agricultural purposes. Potential human exposure pathways include ingestion, inhalation, and dermal contact with contaminated on-site soil and groundwater. The site poses a potential risk to human health because of possible exposures to contaminants at concentrations that may result in adverse health effects. Proposed remedial plans should reduce or eliminate potential risk.

  7. Hydrogen Isotope Exchange of Chlorinated Ethylenes in Aqueous Solution: Possibly a Termolecular Liquid Phase Reaction.

    PubMed

    Gabričević, Mario; Lente, Gábor; Fábián, István

    2015-12-24

    This work reports an experimental study of the hydrogen/deuterium exchange in the basic aqueous solutions of trichloroethylene, trans-1,2-dichloroethylene, and cis-1,2-dichloroethylene using (1)H NMR as a monitoring method. 1,1-Dichlorethylene was also investigated but found not to exchange hydrogen isotopes with water. The kinetics of isotope exchange features two different pathways, the first is first order with respect to hydroxide ion, whereas the second is second order. The first pathway is interpreted as a straightforward bimolecular reaction between chloroethylene and hydroxide ion, which leads to the deprotonation of chloroethylene. The second pathway involves a transition state with the association of one molecule of the chloroethylene and two hydroxide ions. It is shown that the second pathway could involve the formation of a precursor complex composed of one chloroethylene molecule and one hydroxide ion, but a direct termolecular elementary reaction is also feasible, which is shown by deriving a theoretical highest limit for the rate constants of termolecular reactions in solution. PMID:26618984

  8. Mixed Waste Management Facility (MWMF) groundwater monitoring report, second quarter 1992

    SciTech Connect

    Not Available

    1992-09-01

    During second quarter 1992, tritium, trichloroethylene, tetrachloroethylene, chloroethene, antimony, 1,1-dichloroethylene, lead, nonvolatile beta, radium-228, thorium-228, or total alpha-emitting radium (radium-226 and radium-228) exceeded the US Environmental Protection Agency Primary Drinking Water Standards (PDWS) in groundwater samples from monitoring wells at the Mixed Waste Management Facility (MWMF) and adjacent facilities. Tritium and trichloroethylene were the most widespread constituents; 55 (48%) of the 115 monitored wells contained elevated tritium activities, and 23 (20%) wells exhibited elevated trichloroethylene concentrations. Sixty-three downgradient wells screened in Aquifer Zone IIB2 (Water Table), Aquifer Zone IIB[sub 2] (Barnwell/McBean), and Aquifer Unit IIA (Congaree) contained concentrations of tritium, trichloroethylene, tetrachloroethylene, chloroethene, antimony, 1,1-dichloroethylene, lead, nonvolatile beta, radium-228, thorium-228, or total alpha-emitting radium that exceeded the PDWS during second quarter 1992. Upgradient wells BGO 1D and 2D and HSB 85A, 85B, and 85C did not contain any constituents that exceeded the PDWS.

  9. Mixed Waste Management Facility groundwater monitoring report. Second quarter 1994

    SciTech Connect

    Chase, J.A.

    1994-09-01

    Currently, 125 wells monitor groundwater quality in the uppermost aquifer beneath the Mixed Waste Management Facility (MWMF) at the Savannah River Site. Samples from the wells are analyzed for selected heavy metals, indicator parameters, radionuclides, volatile organic compounds, and other constituents. During second quarter 1994, chloroethene (vinyl chloride), 1,1-dichloroethylene, gross alpha, lead, tetrachloroethylene, trichloroethylene, or tritium exceeded final Primary Drinking Water Standards (PDWS) in approximately half of the downgradient wells at the MWMF. Consistent with historical trends, elevated constituent levels were found primarily in Aquifer Zone. As in previous quarters, tritium and trichloroethylene were the most widespread elevated constituents during second quarter 1994. Sixty-two of the 125 monitoring wells contained elevated tritium activities. Trichloroethylene concentrations exceeded the final PDWS in 23 wells. Chloroethene, 1,1-dichloroethylene, lead, and tetrachloroethylene, elevated in one or more wells during second quarter 1994, also occurred in elevated levels during first quarter 1994. These constituents generally were elevated in the same wells during both quarters. Gross alpha, which was not elevated in any well during first quarter 1994, was elevated in one well during second quarter. Copper, mercury, and nonvolatile beta were elevated during first quarter 1994 but not during second quarter.

  10. Mixed Waste Management Facility (MWMF) groundwater monitoring report, second quarter 1992

    SciTech Connect

    Not Available

    1992-09-01

    During second quarter 1992, tritium, trichloroethylene, tetrachloroethylene, chloroethene, antimony, 1,1-dichloroethylene, lead, nonvolatile beta, radium-228, thorium-228, or total alpha-emitting radium (radium-226 and radium-228) exceeded the US Environmental Protection Agency Primary Drinking Water Standards (PDWS) in groundwater samples from monitoring wells at the Mixed Waste Management Facility (MWMF) and adjacent facilities. Tritium and trichloroethylene were the most widespread constituents; 55 (48%) of the 115 monitored wells contained elevated tritium activities, and 23 (20%) wells exhibited elevated trichloroethylene concentrations. Sixty-three downgradient wells screened in Aquifer Zone IIB2 (Water Table), Aquifer Zone IIB{sub 2} (Barnwell/McBean), and Aquifer Unit IIA (Congaree) contained concentrations of tritium, trichloroethylene, tetrachloroethylene, chloroethene, antimony, 1,1-dichloroethylene, lead, nonvolatile beta, radium-228, thorium-228, or total alpha-emitting radium that exceeded the PDWS during second quarter 1992. Upgradient wells BGO 1D and 2D and HSB 85A, 85B, and 85C did not contain any constituents that exceeded the PDWS.

  11. Health assessment for the Transicoil, Inc. (Zone 12) North Penn Area Site, Worchester, Pennsylvania, Region 3. CERCLIS No. PAD057152365. Preliminary report

    SciTech Connect

    Not Available

    1988-09-29

    The Transicoil Inc. (Zone 12) North Penn Area Site consists of a manufacturing site for DC and synchro electric motors for commercial and defense uses. An on-site underground storage tank was used for waste oil and hazardous substances. On-site cesspools were used for sanitary waste disposal. Identified contaminants of concern to data include trichloroethylene (TCE), 1,1,1-trichloroethane, tetrachloroethylene (PCE), cis-1,2-dichloroethylene, 1,1-dichloroethane, and 1,1-dichloroethylene in well water and TCE, PCE, and 1,1,1-trichloroethane in soil. The site is considered to be of potential public health concern because of the risk to human health caused by the possibility of exposure to hazardous substances via ingestion of contaminated groundwater, surface water, or other materials or of plants or animals which have accumulated contaminants from the site; contaminated soil ingestion by children; inhalation of compounds volatilized from contaminated groundwater during household uses, of contaminants volatilized from the site, or of contaminants carried in reentrained dust; and dermal contact with contaminated groundwater, surface water, soil, or other materials.

  12. Kinetics of chlorinated hydrocarbon degradation by Methylosinus trichosporium OB3b and toxicity of trichloroethylene.

    PubMed Central

    Oldenhuis, R; Oedzes, J Y; van der Waarde, J J; Janssen, D B

    1991-01-01

    The kinetics of the degradation of trichloroethylene (TCE) and seven other chlorinated aliphatic hydrocarbons by Methylosinus trichosporium OB3b were studied. All experiments were performed with cells grown under copper stress and thus expressing soluble methane monooxygenase. Compounds that were readily degraded included chloroform, trans-1,2-dichloroethylene, and TCE, with Vmax values of 550, 330, and 290 nmol min-1 mg of cells-1, respectively. 1,1-Dichloroethylene was a very poor substrate. TCE was found to be toxic for the cells, and this phenomenon was studied in detail. Addition of activated carbon decreased the acute toxicity of high levels of TCE by adsorption, and slow desorption enabled the cells to partially degrade TCE. TCE was also toxic by inactivating the cells during its conversion. The degree of inactivation was proportional to the amount of TCE degraded; maximum degradation occurred at a concentration of 2 mumol of TCE mg of cells-1. During conversion of [14C]TCE, various proteins became radiolabeled, including the alpha-subunit of the hydroxylase component of soluble methane monooxygenase. This indicated that TCE-mediated inactivation of cells was caused by nonspecific covalent binding of degradation products to cellular proteins. Images PMID:2036023

  13. Microcosm and in situ field studies of enhanced biotransformation of trichloroethylene by phenol-utilizing microorganisms.

    PubMed Central

    Hopkins, G D; Semprini, L; McCarty, P L

    1993-01-01

    The ability of different aerobic groundwater microorganisms to cometabolically degrade trichloroethylene (TCE), 1,2-cis-dichloroethylene (c-DCE), and 1,2-trans-dichloroethylene (t-DCE) was evaluated both in groundwater-fed microcosms and in situ in a shallow aquifer. Microcosms amended with phenol or toulene were equally effective in removing c-DCE (> 90%) followed by TCE (60 to 70%), while the microcosm fed methane was most effective in removing t-DCE (> 90%). The microcosm fed ammonia was the least effective. None of the microcosms effectively degraded 1,1,1-trichloroethane. At the Moffett Field groundwater test site, in situ removal of c-DCE and TCE coincided with biostimulation through phenol and oxygen injection and utilization, with c-DCE removed more rapidly than TCE. Greater TCE and c-DCE removal was observed when the phenol concentration was increased. Over 90% removal of c-DCE and TCE was observed in the 2-m biostimulated zone. This compares with 40 to 50% removal of c-DCE and 15 to 25% removal of TCE achieved by methane-grown microorganisms previously evaluated in an adjacent in situ test zone. The in situ removal with phenol-grown microorganisms agrees qualitatively with the microcosm studies, with the rates and extents of removal ranked as follows: c-DCE > TCE > t-DCE. These studies demonstrate the potential for in situ TCE bioremediation using microorganisms grown on phenol. PMID:8357259

  14. Anaerobic biodegradation and hydrogeochemical controls on natural attenuation of trichloroethene in an inland forested wetland

    USGS Publications Warehouse

    Lorah, M.M.; Dyer, L.J.; Burris, D.R.

    2007-01-01

    Anaerobic biodegradation was conducted in a forested wetland where a plume of trichloroethylene discharges from a sand aquifer through organic-rich wetland and stream-bottom sediments. The rapid response of the wetland hydrology to precipitation events altered groundwater flow and geochemistry during wet conditions in the spring compared to the drier conditions in the summer and fall. During dry conditions, partial reductive dechlorination of trichloroethylene to cis-1,2-dichloroethylene occurred in methanogenic wetland porewater. Influx of oxygenated recharge during wet conditions led to a change from methanogenic to iron-reducing conditions and a lack of 1,2-dichloroethylene production in the wet spring conditions. During these wet conditions, dilution was the primary attenuation mechanism evident for trichloroethylene in the wetland porewater. Trichloroethylene degradation was insignificant in anaerobic microcosms constructed with the shallow wetland sediment. Natural attenuation of chlorinated solvents by anaerobic biodegradation may not be efficient at all wetland sites, despite organic-rich characteristics of the sediment.

  15. Biodegradation of trichloroethylene and its anaerobic daughter products in freshwater wetland sediments

    USGS Publications Warehouse

    Lorah, M.M.; Olsen, L.D.

    2001-01-01

    Laboratory microcosms were prepared under methanogenic, sulfate-reducing, and aerobic conditions using sediment and groundwater from a freshwater wetland that is a discharge area for a trichloroethylene (TCE) to evaluate potential biodegradation rates of TCE and its anaerobic daughter products (cis-1,2-dichloroethylene, trans-1,2-dichloroethylene, and vinyl chloride (VC)). Anaerobic degradation of TCE was about an order of magnitude faster under methanogenic conditions than under sulfate-reducing conditions. Both 12DCE and VC were found under sulfate-reducing conditions in the microcosms containing the wetland sediment, but their production, especially for VC, was substantially slower than under methanogenic conditions. Methane concentrations remained approximately constant (when losses in the formalin-amended controls are considered) in the microcosms amended with TCE and increased in the microcosms amended with the 12DCE isomers and VC during the first 18-25 days of incubation. The most rapid decrease in concentrations of TCE, cis-12DCE, trans-12DCE, and VC was found after aerobic methane-oxidizing conditions were definitely established.

  16. Sanitary Landfill Groundwater Monitoring Report, Fourth Quarter 1999 and 1999 Summary

    SciTech Connect

    Chase, J.

    2000-03-13

    A maximum of thirty eight-wells of the LFW series monitor groundwater quality in the Steed Pond Aquifer (Water Table) beneath the Sanitary Landfill Area at the Savannah River Site (SRS). These wells are sampled quarterly to comply with the South Carolina Department of Health and Environmental Control Domestic Water Permit DWP-087A and as part of the SRS Groundwater Monitoring Program. Iron (Total Recoverable), Chloroethene (Vinyl Chloride) and 1,1-Dichloroethane were the most widespread constituents exceeding the Final Primary Drinking Water Standards during 1999. Trichloroethylene, 1,1-Dichloroethylene, 1,2-Dichloroethane, 1,4-Dichlorobenzene, Aluminum (Total Recoverable), Benzene, cis-1,2-Dichloroethylene, Dichlorodifluoromethane, Dichloromethane (Methylene Chloride), Gross Alpha, Mercury (Total Recoverable), Nonvolatile Beta, Tetrachloroethylene, Total Organic Halogens, Trichlorofluoromethane, Tritium also exceeded standards in one or more wells. The groundwater flow direction in the Steed Pond Aquifer (Water Table) beneath the Sanitary Landfill is to the southeast (universal transverse Mercator coordinates). The flow rate in this unit was approximately 144.175 ft/year during first quarter 1999 and 145.27 ft/year during fourth quarter 1999.

  17. Effects of adrenolytic mitotane on drug elimination pathways assessed in vitro.

    PubMed

    Theile, Dirk; Haefeli, Walter Emil; Weiss, Johanna

    2015-08-01

    Mitotane (1,1-dichloro-2-(o-chlorophenyl)-2-(p-chlorophenyl)ethane, o,p'-DDD) represents one of the most active drugs for the treatment of adrenocortical carcinoma. Its metabolites 1,1-(o,p'-dichlorodiphenyl) acetic acid (=o,p'-DDA) and 1,1-(o,p'-dichlorodiphenyl)-2,2 dichloroethene (=o,p'-DDE) partly contribute to its pharmacological effects. Because mitotane has a narrow therapeutic index and causes pharmacokinetic drug-drug interactions, knowledge about these compounds' effects on drug metabolizing and transporting proteins is crucial. Using quantitative real-time polymerase chain reaction, our study confirmed the strong inducing effects of o,p'-DDD on mRNA expression of cytochrome P450 3A4 (CYP3A4, 30-fold) and demonstrated that other enzymes and transporters are also induced (e.g., CYP1A2, 8.4-fold; ABCG2 (encoding breast resistance cancer protein, BCRP), 4.2-fold; ABCB1 (encoding P-glycoprotein, P-gp) 3.4-fold). P-gp induction was confirmed at the protein level. o,p'-DDE revealed a similar induction profile, however, with less potency and o,p'-DDA had only minor effects. Reporter gene assays clearly confirmed o,p'-DDD to be a PXR activator and for the first time demonstrated that o,p'-DDE and o,p'-DDA also activate PXR albeit with lower potency. Using isolated, recombinant CYP enzymes, o,p'-DDD and o,p'-DDE were shown to strongly inhibit CYP2C19 (IC50 = 0.05 and 0.09 µM). o,p'-DDA exhibited only minor inhibitory effects. In addition, o,p'-DDD, o,p'-DDE, and o,p'-DDA are demonstrated to be neither substrates nor inhibitors of BCRP or P-gp function. In summary, o,p'-DDD and o,p'-DDE might be potential perpetrators in pharmacokinetic drug-drug interactions through induction of drug-metabolizing enzymes or drug transporters and by potent inhibition of CYP2C19. In tumors over-expressing BCRP or P-gp, o,p'-DDD and its metabolites should retain their efficacy due to a lack of substrate characteristics. PMID:25542188

  18. Neurochemical targets and behavioral effects of organohalogen compounds: an update.

    PubMed

    Mariussen, E; Fonnum, F

    2006-03-01

    Organohalogen compounds (OHCs) have been used and still are used extensively as pesticides, flame retardants, hydraulic fluids, and in other industrial applications. These compounds are stable, most often lipophilic, and may therefore easily biomagnify. Today these compounds are found distributed both in human tissue, including breast milk, and in wildlife animals. In the late 1960s and early 1970s, high levels of the polychlorinated biphenyls (PCBs) and the pesticide dichlorodiphenyl trichloroethane (DDT) were detected in the environment. In the 1970s it was discovered that PCBs and some chlorinated pesticides, such as lindane, have neurotoxic potentials after both acute and chronic exposure. Although the use of PCBs, DDT, and other halogenated pesticides has been reduced, and environmental levels of these compounds are slowly diminishing, other halogenated compounds with potential of toxic effects are being found in the environment. These include the brominated flame retardants, chlorinated paraffins (PCAs), and perfluorinated compounds, whose levels are increasing. It is now established that several OHCs have neurobehavioral effects, indicating adverse effects on the central nervous system (CNS). For instance, several reports have shown that OHCs alter neurotransmitter functions in CNS and Ca2+ homeostatic processes, induce protein kinase C (PKC) and phospholipase A2 (PLA2) mobilization, and induce oxidative stress. In this review we summarize the findings of the neurobehavioral and neurochemical effects of some of the major OHCs with our main focus on the PCBs. Further, we try to elucidate, on the basis of available literature, the possible implications of these findings on human health. PMID:16686424

  19. A comparison of the concentrations of certain chlorinated hydrocarbons and polychlorinated biphenyls in bone marrow and fat tissue of children and their concentrations in breast milk

    SciTech Connect

    Scheele, J.; Teufel, M.; Niessen, K.H.

    1995-12-31

    Chlorinated hydrocarbon (CHC) and polychlorinated biphenyl (PCB) concentrations in the bone marrow of 57 children were compared with the concentrations in adipose tissue of 50 children and the concentrations in breast milk in the Federal Republic of Germany from 1984 to 1991. The concentrations of hexachlorobenzene (HCB), the dichlorodiphenyl-trichlorethane (DDT)-metabolites, and polychlorinated biphenyl (PCB) congeners no. 138 and no. 153 were increased threefold, while the concentrations of several hexachloro-cyclohexane (HCH)-isomers and PCB congener no. 180 were only increased two fold. Because breast feeding is the primary source of CHC and PCB in toddlers and infants we also compared the concentrations in bone marrow of children with the concentrations in breast milk and found approximately fourfold higher concentrations for the most highly chlorinated PCB congener no. 180, but only threefold higher concentrations for PCB 138 and 153 and the DDT-metabolites. The concentrations of {beta}-HCH and HCB were only slightly higher in bone marrow. 15 refs., 2 figs.

  20. Persistent organochlorine compounds in peregrine falcon (Falco peregrinus) eggs from South Greenland: levels and temporal changes between 1986 and 2003.

    PubMed

    Vorkamp, Katrin; Thomsen, Marianne; Møller, Søren; Falk, Knud; Sørensen, Peter B

    2009-02-01

    Thirty-seven addled peregrine falcon eggs collected in South Greenland between 1986 and 2003 were analysed for their content of the organochlorine compounds polychlorinated biphenyls (PCBs), dichlorodiphenyl tricloroethane (DDT) and its degradation products, hexachlorocyclohexane (HCH) isomers and hexachlorobenzene (HCB). PCBs and DDT (including metabolites) were by far the most abundant OC groups, with median concentrations of 55 and 40 microg/g lw, respectively. The concentrations were high in an Arctic context, but similar to previously reported levels from Alaska and Norway and slightly lower than concentrations measured in eggs from industrialised regions. Geographical differences may be of importance, considering the migration of peregrine falcons and their prey. SigmaHCH and HCB had median concentrations of 0.39 and 0.17 microg/g lw, respectively. On average, DDE accounted for 97% of SigmaDDT, but was below critical levels for eggshell thinning. All compound groups showed a weak decreasing trend over the study period, which was statistically significant for HCB and close to being significant for SigmaHCH. The weak decrease of SigmaPCB and SigmaDDT is different from other time trend studies from Greenland, usually showing a more pronounced decrease in the beginning of the study period, followed by a certain stabilisation in recent years. PMID:18823663

  1. Persistent organic pollutants in meat, liver, tallow and bone marrow from semi-domesticated reindeer (Rangifer tarandus tarandus L.) in Northern Norway

    PubMed Central

    2013-01-01

    Background The aim of this project was to study 14 polychlorinated biphenyls (PCBs), 5 dichlorodiphenyl trichloroethans (DDTs), 12 organochlorine pesticides (OCPs) and 6 polybrominated diphenylethers (PBDEs) in meat, liver, tallow and bone marrow from semi-domesticated reindeer. Methods Meat, liver, tallow, and bone marrow samples (n= 30) were collected from semi-domesticated reindeer in Northern Norway. Determination of the persistent organic pollutants (POPs) concentrations was done by using gas chromatography–mass spectrometry (GC-MS). Dependent sample t-test and Pearson’s correlation test were used in statistical analysis. Results Concentrations of the persistent organic pollutants in the samples from semi-domesticated reindeer were generally low and slightly above the limit of detection (LOD). For PCBs and OCPs, ≥ 50% of the samples had concentrations above LOD. For the DDTs and PBDEs, the proportion of samples with concentrations above LOD varied between 3.7 and 45.5% depending on the sample type. Concentrations of PCB 99, 105, 138/163, 153 and 187 differed significantly between meat and liver, whereas concentrations of PCB 183 were significantly different between tallow and bone marrow. Furthermore, concentrations of hexachlorobenzene (HCB) were significantly different between meat and liver. Significant correlations were revealed in concentrations of 5 PCB congeners between the studied tissue types. Conclusion Concentrations of the POPs revealed in this study were generally low. PMID:23938064

  2. Chemical contamination of free-range eggs from Belgium.

    PubMed

    Van Overmeire, I; Pussemier, L; Hanot, V; De Temmerman, L; Hoenig, M; Goeyens, L

    2006-11-01

    The elements manganese, cobalt, nickel, copper, zinc, arsenic, selenium, molybdenum, cadmium, antimony, thallium, lead and mercury, and selected persistent organochlorine compounds (dioxins, marker and dioxin-like polychlorinated biphenyls, dichlorodiphenyltricholroethane (DDT) and metabolites as well as other chlorinated pesticides) were analysed in Belgian free-range eggs obtained from hens of private owners and of commercial farms. It was found that eggs from private owners were more contaminated than eggs from commercial farms. The ratios of levels in eggs from private owners to the levels in eggs from commercial farms ranged from 2 to 8 for the toxic contaminants lead, mercury, thallium, dioxins, polychlorinated biphenyls and the group of DDT. DDT contamination was marked by the substantial presence of p,p'-DDT in eggs from private owners in addition to dichlorodiphenyldichloroethylene (p,p-DDE) and dichlorodiphenyl-dichloroethane (p,p'-DDD). It is postulated that environmental pollution is at the origin of the higher contamination of eggs from private owners. Extensive consumption of eggs from private owners is likely to result in toxic equivalent quantity intake levels exceeding the tolerable weekly intake. PMID:17071513

  3. The potentiality of botanicals and their products as an alternative to chemical insecticides to sandflies (Diptera: Psychodidae): a review.

    PubMed

    Dinesh, Diwakar Singh; Kumari, Seema; Kumar, Vijay; Das, Pradeep

    2014-03-01

    Use of chemical pesticides is the current method for controlling sandflies. However, resistance is being developed in sandflies against the insecticide of choice that is DDT (dichlorodiphenyl trichloroethane). Botanicals have potential to act as an alternative to chemical insecticides as the crude extracts and active molecules of some plants show insecticidal effect to sandflies. This will lead to safe, easy and environment friendly method for control of sandflies. Therefore, information regarding botanicals acting as alternative to chemical insecticide against sandflies assumes importance in the context of development of resistance to insecticides as well as to prevent environment from contamination. This review deals with some plants and their products having repellent and insecticidal effect to sandflies in India and abroad. Different methods of extraction and their bioassay on sandflies have been emphasized in the text. Various extracts of some plants like Ricinus communis (Euphorbiaceae), Solanum jasminoides (Solanaceae), Bougainvillea glabra (Nyctaginaceae), Capparis spinosa (Capparidaceae), Acalypha fruticosa (Euphorbiaceae) and Tagetes minuta (Asteraceae) had shown repellent/insecticidal effect on sandflies. This review will be useful in conducting the research work to find out botanicals of Indian context having insecticidal effect on sandflies. PMID:24717195

  4. An exploration of the estrogen receptor transcription activity of capsaicin analogues via an integrated approach based on in silico prediction and in vitro assays.

    PubMed

    Li, Juan; Ma, Duo; Lin, Yuan; Fu, Jianjie; Zhang, Aiqian

    2014-06-16

    Capsaicin has been considered as an alternative template of dichlorodiphenyl trichloroethane (DDT) in antifouling paint. However, information regarding the estrogenic activity of capsaicin analogues is rather limited in comparison to that of DDT analogues and their metabolites. We here explore the ER transcription activity of selected capsaicin analogues via an integrated approach based on in silico prediction and in vitro assays. Molecular simulation and the agonist/antagonist differential-docking screening identified 6-iodonordihydrocapsaicin (6-I-CPS) as a weak ERα agonist, while anti-estrogenicity was expected for N-arachidonoyldopamine, capsazepine, dihydrocapsaicin, trichostatin A, and capsaicin. On the contrary, the large volume of analogues, such as phorbol 12-phenylacetate 13-acetate 20-homovanillate and phorbol 12,13-dinonanoate 20-homovanillate, cannot fit well with the ER cavity. The result of MVLN assay was in accord with the in silico prediction. 6-I-CPS was demonstrated to induce luciferase gene expression, while the other analogues of relatively small molecular volume reduced luciferase gene expression in MVLN cells, both in the absence and presence of estradiol. This finding suggested that the ER transcription activity of capsaicin analogues is generated at least partly through the ERα-mediated pathway. Moreover, receptor polymorphism analysis indicated that capsaicin analogues may exhibit diverse species selectivity for human beings and marine species. PMID:24747365

  5. POST-REMEDIATION BIOMONITORING OF PESTICIDES AND OTHER CONTAMINANTS IN MARINE WATERS AND SEDIMENT NEAR THE UNITED HECKATHORN SUPERFUND SITE, RICHMOND, CALIFORNIA

    SciTech Connect

    Antrim, Liam D.; Kohn, Nancy P.

    2000-09-06

    Marine sediment remediation at the United Heckathorn Superfund Site was completed in April 1997. Water and mussel tissues were sampled in February 1999 from four stations near Lauritzen Canal in Richmond, California, for Year 2 of post-remediation monitoring of marine areas near the United Heckathorn Site. Dieldrin and dichlorodiphenyl trichloroethane (DDT) were analyzed in water samples, tissue samples from resident mussels, and tissue samples from transplanted mussels deployed for 4 months. Mussel tissues were also analyzed for polychlorinated biphenyls (PCB), which were detected in sediment samples. Chlorinated pesticide concentrations in water samples were similar to preremediation levels and did not meet remediation goals. Biomonitoring results indicated that the bioavailability of chlorinated pesticides has been reduced from preremediation levels both in the dredged area and throughout Richmond Harbor. Total DDT and dieldrin concentrations in mussel tissues were lower than measured levels from preremediation surveys and also lower than Year 1 levels from post-remediation biomonitoring. Sediment analyses showed the presence of elevated DDT, dieldrin, PCB aroclor 1254, and very high levels of polynuclear aromatic hydrocarbons (PAH) in Lauritzen Channel.

  6. Spatial distribution of polychlorinated biphenyls, organochlorine pesticides, and dechlorane plus in Northeast Asia

    NASA Astrophysics Data System (ADS)

    Baek, Song-Yee; Jurng, Jongsoo; Chang, Yoon-Seok

    2013-01-01

    XAD-2 resin-based passive air samplers (PAS) were deployed for one year at eight cities in Mongolia, China, and South Korea to investigate the spatial distribution of polychlorinated biphenyls (PCBs), organochlorine pesticides (OCPs), and dechlorane plus (DP). PCB levels were highly correlated with population size and density in China and South Korea. In Mongolia, PCB levels were relatively high considering the low population. In the cases of OCPs and DP, a country-specific distribution was observed. The highest levels of HCHs (hexachlorocyclohexane isomers) and DDTs (dichlorodiphenyl trichloroethane isomers) were detected at sites in China, whereas the highest endosulfan and DP levels were measured at South Korean sites. These results strongly reflected the patterns of use of these chemicals. Mirex, an insecticide never registered in Mongolia and South Korea, was detected at all sampling sites; this is likely to have resulted from long-range transport. Nevertheless, OCPs were generally low in Mongolia. This study confirms that PAS results reflect well the past and current usage of POPs in Northeast Asia.

  7. DDE and shortened duration of lactation in a northern Mexican town.

    PubMed Central

    Gladen, B C; Rogan, W J

    1995-01-01

    OBJECTIVES. Worldwide declines in the duration of lactation are cause for public health concern. Higher levels of dichlorodiphenyl dichloroethene (DDE) have been associated with shorter durations of lactation in the United States. This study examined whether this relationship would hold in an agricultural town in northern Mexico. METHODS. Two hundred twenty-nine women were followed every 2 months from childbirth until weaning or until the child reached 18 months of age. DDE was measured in breast milk samples taken at birth, and women were followed to see how long they lactated. RESULTS. Median duration was 7.5 months in the lowest DDE group and 3 months in the highest. The effect was confined to those who had lactated previously, and it persisted after statistical adjustment for other factors. These results are not due to overtly sick children being weaned earlier. Previous lactation lowers DDE levels, which produces an artifactual association, but simulations using best estimates show that an effect as large as that found here would arise through this mechanism only 6% of the time. CONCLUSIONS. DDE may affect women's ability to lactate. This exposure may be contributing to lactation failure throughout the world. PMID:7702113

  8. Impact of turbidity on TCE and degradation products in ground water

    SciTech Connect

    Paul, C.J.; Puls, R.W.

    1997-06-01

    Elevated particulate concentrations in ground water samples can bias contaminant concentration data. This has been particularly problematic for metal analyses where artificially increased turbidity levels can affect metals concentrations and confound interpretation of the data. However, few studies have been conducted to determine the impact of particulates on trichloroethylene (TCE), cis-dichloroethylene (c-DCE), and vinyl chloride concentrations. Laboratory batch studies and field investigations were conducted to evaluate the effects of suspended solids on VOC concentrations in ground water samples analyzed by purge-and-trap gas chromatography. Three different solids were used to assess the effects of suspended particulates. The solids were aquifer material from a field site in North Carolina and two reference clay minerals (kaolinite and Na-montmorillonite). During the laboratory portion of this study, the solids were used to determine effects on TCE concentrations under controlled laboratory conditions. The same solids were used in a field study to compare the laboratory results with field results.

  9. An Evaluation of Microbial and Chemical Contamination Sources Related to the Deterioration of Tap Water Quality in the Household Water Supply System

    PubMed Central

    Lee, Yoonjin

    2013-01-01

    The predominant microorganisms in samples taken from shower heads in residences in the Korean city “N” were Stenotrophomonas maltophilia, Sphingomonas paucimobilis, Acidovorax temperans, and Microbacterium lacticum. Legionella was not detected in this case. The volatile organic compounds (VOCs) vinylacetate, NN-DMA, cis-1,2-dichloroethylene, epichlorohydrin, and styrene were measured in five types of plastic pipes: PVC, PB, PP, PE, and cPVC. The rate of multiplication of the heterotrophic plate count (HPC) attached on the copper pipe in contact with hot tap water was higher than the rate for the copper pipe in contact with cold tap water. Biofilm accumulation on stainless steel pipes with added acetate (3 mg/L) was 2.56 times higher than the non-supplemented condition. Therefore, the growth of HPC in the pipe system was affected by the type and availability of nutrients and depended on variables such as heating during the hot water supply. PMID:24018837

  10. Health assessment for Laurel Park Landfill, Naugatuck, Connecticut, Region 1. CERCLIS No. CTD980521165. Final report

    SciTech Connect

    Not Available

    1986-12-04

    The Environmental Protection Agency, Region I, submitted the Endangerment Assessment Report and Remedial Investigation Report for the Laurel Park Landfill, a National Priority List site, to the Agency for Toxic Substances and Disease Registry for review. Based on the information provided, additional monitoring data is needed to determine the extent and degree of contamination in order to properly assess endangerment of public health. However, the current maximum contaminant levels found in on-site soil and leachate (i.e., arsenic, chromium, 1,2-dichloroethane, benzene, 1,2-dichloroethylene, n-nitrosodiphenylamine, 2,4-dichlorophenol) pose a potential public health threat. Therefore, public access to the contaminated areas should be restricted.

  11. Quarterly sampling of the wetlands along the old F-Area effluent ditch: August 1994. Revision 1

    SciTech Connect

    Cummins, C.L.; Dixon, K.L.

    1994-08-01

    In August 1994, well point water and near-surface water samples were collected to further characterize tritium and volatile organic compounds in the Wetlands along the old F-Area effluent ditch south of 643-E at the Savannah River Plant. Well point samples were collected from seven locations and near-surface water samples were collected at four locations. Results of the August 1994 sampling event further support findings that tritium and volatile organic compounds are outcropping in the Wetlands near the old F-area effluent ditch. Four analytes (1,2-dichloroethylene, trichloroethylene, tritium, and vinyl chloride) were detected at least once at concentrations above the primary Drinking Water Standards or the Maximum Contaminant Levels. Five analytes (the above chemicals plus tetrachloroethylene) were detected at least once in the near-surface water samples at concentrations greater than the method detection limit.

  12. Mixed Waste Management Facility (MWMF) groundwater monitoring report

    SciTech Connect

    Thompson, C.Y.

    1992-12-01

    During third quarter 1992, 12 constituents exceeded the US Environmental Protection Agency Primary Drinking Water Standards (PDWS) in one or more groundwater samples from monitoring wells at the Mixed Waste Management Facility and adjacent facilities. Tritium and trichloroethylene were the most widespread constituents: 57 (48%) and 23 (19%) of the 119 monitoring wells contained elevated tritium and trichloroethylene levels, respectively. Elevated constituents were found primarily in Aquifer Zone IIB[sub 2] (Water Table) and Aquifer Zone IIB[sub 1] (Barnwell/McBean). Elevated constituents also occurred in five Aquifer Unit IIA (Congaree) wells. Upgradient wells BGO 1D and 2D and HSB 85A, 85B, and 85C did not contain any constituents that exceeded the PDWS. Downgradient wells in the three hydrostratigraphic units contained elevated levels of tritium, trichloroethylene, tetrachloroethylene, chloroethene, antimony, 1,1-dichloroethylene, gross alpha, lead, nonvolatile beta, thallium, total alpha-emitting radium (radium-224 and radium-226), or cadmium.

  13. Mixed Waste Management Facility (MWMF) groundwater monitoring report. Third quarter 1992

    SciTech Connect

    Thompson, C.Y.

    1992-12-01

    During third quarter 1992, 12 constituents exceeded the US Environmental Protection Agency Primary Drinking Water Standards (PDWS) in one or more groundwater samples from monitoring wells at the Mixed Waste Management Facility and adjacent facilities. Tritium and trichloroethylene were the most widespread constituents: 57 (48%) and 23 (19%) of the 119 monitoring wells contained elevated tritium and trichloroethylene levels, respectively. Elevated constituents were found primarily in Aquifer Zone IIB{sub 2} (Water Table) and Aquifer Zone IIB{sub 1} (Barnwell/McBean). Elevated constituents also occurred in five Aquifer Unit IIA (Congaree) wells. Upgradient wells BGO 1D and 2D and HSB 85A, 85B, and 85C did not contain any constituents that exceeded the PDWS. Downgradient wells in the three hydrostratigraphic units contained elevated levels of tritium, trichloroethylene, tetrachloroethylene, chloroethene, antimony, 1,1-dichloroethylene, gross alpha, lead, nonvolatile beta, thallium, total alpha-emitting radium (radium-224 and radium-226), or cadmium.

  14. {gamma} Irradiation-induced degradation of organochlorinated pollutants in fatty esters and in Cod

    SciTech Connect

    Lepine, F.L.; Brochu, F.; Milot, S.

    1995-02-01

    The {gamma} irradiation-induced degradation of 2,2-bis(4-chlorophenyl)-1,1,1-trichloroethane (DDT), 2,2-bis(4-chlorophenyl)-1,1-dichloroethane (DDD), and 2,2-bis(4-chlorophenyl)-1,1-dichloroethylene (DDE) dissolved in methyl myristate and methyl oleate was studied. DDT and DDE produced DDD and 2,2-bis(4-chlorophenyl)chloroethylene (DDMU) respectively, in agreement with a previous study performed with aliphatic solvents. The degradation of these two former compounds was larger in methyl myristate than in methyl oleate and addition products between methyl myristate and the organochlorines were found. While DDD, DDE, and many PCB congeners in a cod sample were not measurably degraded at 15 KGy, DDT underwent 30% degradation. 9 refs., 1 fig., 2 tabs.

  15. 20 kHz sonoelectrochemical degradation of perchloroethylene in sodium sulfate aqueous media: influence of the operational variables in batch mode.

    PubMed

    Sáez, Verónica; Esclapez, María Deseada; Tudela, Ignacio; Bonete, Pedro; Louisnard, Olivier; González-García, José

    2010-11-15

    A preliminary study of the 20 kHz sonoelectrochemical degradation of perchloroethylene in aqueous sodium sulfate has been carried out using controlled current density degradation sonoelectrolyses in batch mode. An important improvement in the viability of the sonochemical process is achieved when the electrochemistry is implemented, but the improvement of the electrochemical treatment is lower when the 20 kHz ultrasound field is simultaneously used. A fractional conversion of 100% and degradation efficiency around 55% are obtained independently of the ultrasound power used. The current efficiency is also enhanced compared to the electrochemical treatment and a higher speciation is also detected; the main volatile compounds produced in the electrochemical and sonochemical treatment, trichloroethylene and dichloroethylene, are not only totally degraded, but also at shorter times than in the sonochemical or electrochemical treatments. PMID:20705391

  16. Health assessment for American Lake Gardens, Tacoma, Pierce County, Washington, Region 10. CERCLIS No. WAD980833065. Preliminary report

    SciTech Connect

    Not Available

    1989-01-19

    The American Lake Gardens site is on the National Priorities List. Two areas within the site are the areas of primary contamination; the northeast section's contamination is believed to have come from the closed landfill (now a golf course) on McChord AFB, and the southwest section's contamination from Fort Lewis. Both Fort Lewis and McChord AFB are NPL sites. The environmental contamination on-site consists of trans-1,2-dichloroethylene (530 ppb), trichloroethylene (260 ppb), methylene chloride (38 ppb), tetrachloroethylene (52 ppb), benzene (6 ppb), and 1,1,1-trichloroethane (18 ppb) in ground water. The site is considered to be of potential public health concern because of the risk to human health caused by the possibility of exposure to hazardous substances via ground water (from private wells still in use) and surface water.

  17. Formalin preservation of avian blood for organochlorine analysis

    USGS Publications Warehouse

    Stafford, C.J.; Stickel, W.H.

    1981-01-01

    Blood biopsy for chemical analysis is a valuable technique for evaluating chemical exposure of birds in the wild without harming the birds. Field conditions, however, often make sample storage difficult. Better methods than freezing are needed to improve the interpretive value of chemical analysis of the sample. The use of formalin was explored for this purpose. A pooled sample of blood containing naturally incorporated 1,1-bis-(p-chlorophenyl)-2,2,2-trichloroethane (DDT), 2,2-bis-(p-chlorophenyl)1,1 dichloroethylene (DDE), and dieldrin was subdivided into 30 samples, of which 10 were frozen, 10 more were kept at room temperature, and 10 were formalinized by adding I part of chemically pure formalin to 20 parts of blood. The formalinized samples yielded the highest and least variable concentrations of chemicals. The field procedures are outlined.

  18. Mixed Waste Management Facility (MWMF) groundwater monitoring report. Fourth quarter 1993 and 1993 summary

    SciTech Connect

    Butler, C.T.

    1994-03-01

    During fourth quarter 1993, 10 constituents exceeded final Primary Drinking Water Standards in groundwater samples from downgradient monitoring wells at the Mixed Waste Management Facility, the Old Burial Ground, the E-Area Vaults, and the proposed Hazardous Waste/Mixed Waste Disposal Vaults. As in previous quarters, tritium and trichloroethylene were the most widespread elevated constituents. Carbon tetrachloride, chloroform, chloroethane (vinyl chloride), 1,1-dichloroethylene, dichloromethane (methylene chloride), lead, mercury, or tetrachloroethylene also exceeded standards in one or more wells. Elevated constituents were found in numerous Aquifer Zone 2B{sub 2} (Water Table) and Aquifer Zone 2B{sub 1}, (Barnwell/McBean) wells and in two Aquifer Unit 2A (Congaree) wells. The groundwater flow direction and rates in the three hydrostratigraphic units were similar to those of previous quarters.

  19. Alternative Green Solvents Project

    NASA Technical Reports Server (NTRS)

    Maloney, Phillip R.

    2012-01-01

    Necessary for safe and proper functioning of equipment. Mainly halogenated solvents. Tetrachloride, Trichloroethylene (TCE), CFC-113. No longer used due to regulatory/safety concerns. Precision Cleaning at KSC: Small % of total parts. Used for liquid oxygen (LOX) systems. Dual solvent process. Vertrel MCA (decafluoropentane (DFP) and trons-dichloroethylene) HFE-7100. DFP has long term environmental concerns. Project Goals: a) Identify potential replacements. b) 22 wet chemical processes. c) 3 alternative processes. d) Develop test procedures. e) Contamination and cleaning. f) Analysis. g) Use results to recommend alternative processes. Conclusions: a) No alternative matched Vertrel in this study. b) No clear second place solvent. c) Hydrocarbons- easy; Fluorinated greases- difficult. d) Fluorinated component may be needed in replacement solvent. e) Process may need to make up for shortcoming of the solvent. f) Plasma and SCC02 warrant further testing.

  20. Mixed Waste Management Facility (MWMF) groundwater monitoring report

    SciTech Connect

    Thompson, C.Y.

    1992-06-01

    During first quarter 1992, tritium, trichloroethylene, tetrachloroethylene, lead, antimony, I,I-dichloroethylene, 1,2-dichloroethane, gross alpha, mercury, nickel, nitrate, nonvolatile beta, and total alpha-emitting radium (radium-224 and radium-226) exceeded the US Environmental Protection Agency Primary Drinking Water Standards (PDWS) in groundwater samples from monitoring wells at the Mixed Waste Management Facility (MWMF) and adjacent facilities. Tritium and trichloroethylene were the most widespread constituents; 57 (49%) of the 116 monitored wells contained elevated tritium activities, and 21 (18%) wells exhibited elevated trichloroethylene concentrations Sixty-one downgradient wells screened in Aquifer Zone IIB2 (Water Table), Aquifer Zone IIB[sub 2] (Barnwell/McBean), and Aquifer Unit IIA (Congaree) contained constituents that exceeded the PDWS during first quarter 1992. Upgradient wells BGO 1D and HSB 85A, BC, and 85C did not contain any constituents that exceeded the PDWS. Upgradient well BGO 2D contained elevated tritium.

  1. Mixed Waste Management Facility (MWMF) groundwater monitoring report. First quarter 1992

    SciTech Connect

    Thompson, C.Y.

    1992-06-01

    During first quarter 1992, tritium, trichloroethylene, tetrachloroethylene, lead, antimony, I,I-dichloroethylene, 1,2-dichloroethane, gross alpha, mercury, nickel, nitrate, nonvolatile beta, and total alpha-emitting radium (radium-224 and radium-226) exceeded the US Environmental Protection Agency Primary Drinking Water Standards (PDWS) in groundwater samples from monitoring wells at the Mixed Waste Management Facility (MWMF) and adjacent facilities. Tritium and trichloroethylene were the most widespread constituents; 57 (49%) of the 116 monitored wells contained elevated tritium activities, and 21 (18%) wells exhibited elevated trichloroethylene concentrations Sixty-one downgradient wells screened in Aquifer Zone IIB2 (Water Table), Aquifer Zone IIB{sub 2} (Barnwell/McBean), and Aquifer Unit IIA (Congaree) contained constituents that exceeded the PDWS during first quarter 1992. Upgradient wells BGO 1D and HSB 85A, BC, and 85C did not contain any constituents that exceeded the PDWS. Upgradient well BGO 2D contained elevated tritium.

  2. Sanitary Landfill groundwater monitoring report. Fourth quarterly report and summary 1993

    SciTech Connect

    Not Available

    1994-02-01

    Fifty-seven wells of the LFW series monitor groundwater quality in Steed Pond Aquifer (Water Table) beneath the Sanitary Landfill at the Savannah River Site (SRS). These wells are sampled quarterly to comply with the South Carolina Department of Health and Environmental Control Domestic Waste Permit DWP-087A and as part of the SRS Groundwater Monitoring Program. Dichloromethane a common laboratory contaminant, and trichloroethylene were the most widespread constituents exceeding standards during 1993. Benzene, chlorobenzene, chloroethene 1,2 dichloroethane, 1,1-dichloroethylene, 1,2-dichloropropane, gross alpha, lindane, mercury, tetrachloroethylene, and tritium also exceeded standards in one or more wells. No groundwater contaminants were observed in wells screened in the lower section of Steed Pond Aquifer.

  3. Mixed Waste Management Facility (MWMF) groundwater monitoring report: Third quarter 1993

    SciTech Connect

    Not Available

    1993-12-01

    During third quarter 1993, eight constituents exceeded final Primary Drinking Water Standards in groundwater samples from downgradient monitoring wells at the Mixed Waste Management Facility, the Old Burial Ground, the E-Area Vaults, and the proposed Hazardous Waste/Mixed Waste Disposal Vaults. As in previous quarters, tritium and trichloroethylene were the most widespread constituents Chloroethene (vinyl chloride), 1,1-dichloroethylene, dichloromethane (methylene chloride), lead, mercury, or tetrachloroethylene also exceeded standards in one or more wells. The elevated constituents were found in Aquifer Zone IIB{sub 2} (Water Table) and Aquifer Zone IIB{sub 1} (Barnwell/McBean) wells. No elevated constituents were exhibited in Aquifer Unit IIA (Congaree) wells. The groundwater flow directions and rates in the three hydrostratigraphic units were similar to those of previous quarters.

  4. Health assessment for Whitehall Wells, Whitehall, Michigan, Region 5. CERCLIS No. MID980701254. Preliminary report

    SciTech Connect

    Not Available

    1989-04-14

    The Whitehall Wells (WW) are listed on the National Priorities List. Tap water in Whitehall City was found to contain 4 ppb of perchloroethylene (PCE). Two of the city's five production wells contained up to 6 ppb PCE, and nearby monitor wells contained up to 5 ppb 1,1-dichloroethane, 68 ppb trichloroethylene (TCE), 28 ppb chloroform, and 474 ppb cis-1,2-dichloroethylene. Analysis of soil, surface water, and especially ground water within the City of Whitehall clearly demonstrate the presence of chemical contaminants in the environment. The site is of potential public health concern because of the risk to human health that could result from possible exposure to hazardous substances at levels that may result in adverse health effects over time; human exposure to perchloroethylene has occurred via ground water.

  5. Validation and application of pharmacokinetic models for interspecies extrapolations in toxicity risk assessments of volatile organics. Annual report No. 2, 1 July 1988-30 June 1989

    SciTech Connect

    Dallas, C.E.; Bruckner, J.V.; Gallo, J.; Ramanathan, R.; Muralidhara, S.

    1989-07-21

    In pursuit of the goal of establishing a scientific basis for the interspecies extrapolation of pharmacokinetic data in health-risk assessments, a series of studies were conducted involving pharmacokinetic determinations in rats to several aliphatic halocarbons (with parallel studies initiated in the dog). Direct measurements of the uptake and elimination of halocarbon in rats were completed during the following inhalation exposures and following oral administration of dichloroethylene (DCE) and perchloroethylene (PCE). An assay for the measurement of halocarbons in the tissues of exposed animals has been successfully developed, and tissue-concentration profiles in the liver, kidney, lung, fat, brain, muscle, and heart were completed for oral and intraarterial administrations of PCE. The utility of the physiologically-based pharmacokinetic model for the accurate computer simulations of the pharmacokinetics of three halocarbons with wide variation in physicochemical properties (TRI, TCE, and PCE) has been demonstrated.

  6. Application of fluorescent antibody and enzyme-linked immunosorbent assays for TCE and PAH degrading bacteria

    SciTech Connect

    Brigmon, R.L.; Franck, M.; Brey, J.; Scott, D.; Lanclos, K.; Fliermans, C.

    1996-07-01

    Historically, methods used to identify methanotrophic and polyaromatic hydrocarbon-degrading (PAH) bacteria in environmental samples have been inadequate because isolation and identification procedures are time-consuming and often fail to separate specific bacteria from other environmental microorganisms. Methanotrophic bacteria have been isolated and characterized from TCE-contaminated soils (Bowman et al. 1993; Fliermans et al., 1988). Fliermans et al., (1988) and others demonstrated that cultures enriched with methane and propane could cometabolically degrade a wide variety of chlorinated aliphatic hydrocarbons including ethylene; 1,2-cisdichloroethylene (c-DCE); 1,2-trans-dichloroethylene (t-DCE); vinyl chloride (VC); toluene; phenol and cresol. Characterization of select microorganisms in the natural setting is important for the evaluation of bioremediation potential and its effectiveness. This realization has necessitated techniques that are selective, sensitive and easily applicable to soils, sediments, and groundwater (Fliermans, et al., 1994). Additionally these techniques can identify and quantify microbial types in situ in real time

  7. Phytoremediation of chlorinated ethenes in seepline sediments: tree selection.

    PubMed

    Stanhope, Andrine; Berry, Christopher J; Brigmon, Robin L

    2008-01-01

    Phytoremediation of chlorinated ethene (CE)-contaminated water was investigated at the Savannah River Site in Aiken, SC, USA. Perchloroethylene (PCE) and trichloroethylene (TCE) are present where CE-contaminated groundwater currently outcrops in seepline soils. Results of constructed and planted test cells, filled with soil from a noncontaminated seepline area and supplied with CE-contaminated groundwater (48 ppb) in the field for one season are presented. These test cells were planted with loblolly pines, hybrid poplars, coyote willow, and sweet gum. Cis-dichloroethylene (cDCE), a byproduct from rhizosphere microbial activity, was detected in the soils as well as some tree tissues. All trees tested were found to uptake both PCE and TCE (5-50 pbb/gm dry wt). PMID:19260231

  8. Reactivities of Precision Cleaning Solvents with Hypergolic Propellants

    NASA Technical Reports Server (NTRS)

    Davis, Dennis D.; Delgado, Rafael H.; Williams, James H.

    1999-01-01

    The reactivities of several selected halogenated precision cleaning solvents with hypergolic propellants has been determined by analysis of the rates of formation of halide ion decomposition products. The solvents were Asahiklin AK 225, Asahiklin AK 225 AES, HFE 7100, HFE 7100 DE, Vertrel XF, Vertrel MCA, Vertrel MCA Plus, 1,1,2-trichloro-1,2,2-trifluoroethane (CFC-113), and trans-1,2-dichloroethylene (DCE). The propellants were hydrazine (HZ), monomethylhydrazine (MMH), and mixed oxides of nitrogen (MON-3). The Vertrel solvents showed significant reactivity with HZ. All of the solvents except DCE exhibited significant reactivity with MMH, particularly HFE 7100 DE and CFC-113. HFE 7100 DE, Vertrel MCA, and Vertrel MCA Plus also showed significant reactivity with MON-3 oxidizer.

  9. Sanitary landfill groundwater monitoring report. Fourth quarter 1994 and 1994 summary

    SciTech Connect

    1995-02-01

    Eighty-nine wells of the LFW series monitor groundwater quality in the Steed Pond Aquifer (Water Table) beneath the Sanitary Landfill at the Savannah River Site (SRS). These wells are sampled quarterly to comply with the South Carolina Department of Health and Environmental Control Domestic Waste Permit DWP-087A and as part of the SRS Groundwater Monitoring Program. Dichloromethane, a common laboratory contaminant, and trichloroethylene were the most widespread constituents exceeding standards during 1994. Benzene, chloroethene (vinyl chloride), 1,2-dichloroethane, 1,1-dichloroethylene, 1,2-dichloropropane, gross alpha, mercury, nonvolatile beta, tetrachloroethylene, and tritium also exceeded standards in one or more wells. The groundwater flow direction in the Steed Pond Aquifer (Water Table) beneath the Sanitary Landfill was to the southeast (universal transverse Mercator coordinates). The flow rate in this unit was approximately 140 ft/year during first and fourth quarters 1994.

  10. Mixed Waste Management Facility (MWMF) groundwater monitoring report. First quarter 1993

    SciTech Connect

    Not Available

    1993-06-01

    During first quarter 1993, eight constituents exceeded final Primary Drinking Water Standards in groundwater samples from downgradient monitoring wells at the Mixed Waste anagement Facility, the Old Burial Ground, the E-Area Vaults, and the proposed Hazardous Waste/Mixed Waste Disposal Vaults (HWMWDV). As in previous quarters, tritium and trichloroethylene were the most widespread constituents. Tetrachloroethylene, chloroethene, 1,1-dichloroethylene, gross alpha, lead, or nonvolatile beta levels also exceeded standards in one or more wells. The elevated constituents were found primarily in Aquifer Zone IIB{sub 2} (Water Table) and Aquifer Zone IIB{sub 1}, (Barnwell/McBean) wells. However, several Aquifer Unit IIA (Congaree) wells also contained elevated constituent levels. The groundwater flow directions and rates in the three hydrostratigraphic units were similar to previous quarters.

  11. Recalcitrance of 1,1-dichloro-2,2-bis(p-chlorophenyl)ethylene (DDE) to cometabolic degradation by pure cultures of aerobic and anaerobic bacteria.

    PubMed

    Megharaj, M; Jovcic, A; Boul, H L; Thiele, J H

    1997-08-01

    Pure cultures of aerobic and anaerobic bacteria capable of oxidation and reductive dehalogenation of chloroethylenes, and aerobic bacteria involved in biodegradation of polychlorinated biphenyls (PCBs) were screened for their ability to cometabolize the persistent pollutant 1,1-dichloro-2,2-bis(p-chlorophenyl)ethylene (DDE). Bacterial cultures expressing methane monooxygenase (Methylosinus trichosporium), propane monooxygenase (Mycobacterium vaccae) and biphenyl 2,3-dioxygenase enzymes (Pseudomonas fluorescens and Rhodococcus globerulus), as well as bacteria reductively dechlorinating chloroethylenes (Acetobacterium woodii and Clostridium butyricum) could not degrade DDE. Cell-free extracts of M. trichosporium, M. vaccae, P. fluorescens and R. globerulus were also unable to transform DDE, indicating that cell wall and membrane diffusion barriers were not biodegradation limiting. These studies suggest that these bacteria can not degrade DDE, even when provided with cosubstrates that induce chlorophenyl- and dichloroethylene-group transforming enzymes. PMID:9294241

  12. Characterization of a microbial consortium capable of rapid and simultaneous dechlorination of 1,1,2,2-tetrachloroethane and chlorinated ethane and ethene intermediates

    USGS Publications Warehouse

    Jones, E.J.P.; Voytek, M.A.; Lorah, M.M.; Kirshtein, J.D.

    2006-01-01

    A study was carried out to develop a culture of microorganisms for bioaugmentation treatment of chlorinated-ethane contaminated groundwater at sites where dechlorination is incomplete or rates are too slow for effective remedation. Mixed cultures capable of dechlorinating chlorinated ethanes and ethenes were enriched from contaminated wetland sediment at Aberdeen Proving Ground (APG) Maryland. The West Branch Consortium (WBC-2) was capable of degrading 1,1,2,2-tetrachloroethane (TeCA), trichloroethylene (TCE), cis and trans 1,2-dichloroethylene (DCE), 1,1,2-trichloroethane (TCA), 1,2-dichloroethane, and vinyl chloride to nonchlorinated end products ethylene and ethane. WBC-2 dechlorinated TeCA, TCA, and cisDCE rapidly and simultaneously. Methanogens in the consortium were members of the class Methanomicrobia, which includes acetoclastic methanogens. The WBC-2 consortium provides opportunities for the in situ bioremediation of sites contaminated with mixtures of chlorinated ethylenes and ethanes.

  13. Kinetics of the transformation of trichloroethylene and tetrachloroethylene by iron sulfide

    SciTech Connect

    Butler, E.C.; Hayes, K.F. . Dept. of Civil and Environmental Engineering)

    1999-06-15

    The transformation of trichloroethylene (TCE), tetrachloroethylene (PCE), and 1,1-dichloroethylene FeS in aqueous solution at pH 8.3 was studied in batch experiments. TCE and PCE were transformed by FeS with pseudo-first-order rate constants, corrected for partitioning to the sample headspace, of (1.49 [+-] 0.14) [times] 10[sup [minus]3] h[sup [minus]1] (TCE) and (5.7 [+-] 1.0) [times] 10[sup [minus]4] h[sup [minus]1] (PCE). A 17% decrease in the concentration of 1,3-DCE was observed over 120 days; however, no reaction products were detected. TCE and PCE transformation data were fit to a rate law assuming transformation of TCE via parallel reaction pathways to acetylene and cis-1,2-dichloroethylene (cis-DCE) and transformation of PCE via parallel reaction pathways to acetylene and TCE. Acetylene was the major reaction product for both TCE and PCE. Determination of rate constants for each reaction pathway indicated that TCE was transformed to acetylene 11.8 [+-] 1.1 times faster than to cis-DCE and that PCE was transformed to acetylene 8.2 [+-] 1.8 times faster than to TCE. Additional minor reaction products were vinyl chloride (VC) for TCE and cis-DCE for PCE. Detection of acetylene as the major product of both TCE and PCE transformation by FeS contrasts with the sequential hydrogenolysis products typically observed in the microbial transformation of these compounds, making acetylene a potential indicator of abiotic transformation of TCE and PCE by FeS in natural systems.

  14. Characterization of anaerobic chloroethene-dehalogenating activity in several subsurface sediments

    SciTech Connect

    Skeen, R.S.; Gao, J.; Hooker, B.S.; Quesenberry, R.D.

    1996-11-01

    Anaerobic microcosms of subsurface soils from four locations were used to investigate the separate effects of several electron donors on tetrachloroethylene (PCE) dechlorination activity. The substrates tested were methanol, formate, lactate, acetate, and sucrose. Various levels of sulfate-reducing, acetogenic, fermentative, and methanogenic activity were observed in all sediments. PCE dechlorination was detected in all microcosms, but the amount of dehalogenation varied by several orders of magnitude. Trichloroethylene was the primary dehalogenation product; however, small amounts of cis-1,2-dichloroethylene, 1,1-dichloroethylene, and vinyl chloride were also detected in several microcosms. Lactate-amended microcosms showed large amounts of dehalogenation. in three of the four sediments. One of the two sediments which showed positive activity with lactate also had large amounts of delialogenation with methanol. Sucrose, formate, and acetate also stimulated large amounts of delialogenation in one sediment that showed activity with lactate. These results suggest that lactate may be an appropriate substrate for screening sediments for PCE or TCE delialogenation activity, but that the microbial response is not sufficient for complete in situ bioremediation. A detailed study of the Victoria activity revealed that delialogenation rates were more similar to the Cornell culture than to rates measured for methanogens, or a methanol-enriched sediment culture. This may suggest that these sediments contain a highly efficient delialogenation activity similar to the Cornell culture. This assertion is supported further by the fact that an average of 3% of added reducing equivalents could be diverted to dehalogenation in tests which were conducted using PCE-saturated hexadecane as a constant source of PCE during incubation. Further evidence is needed to confirm this premise. The application of these results to in situ bioremediation of highly contaminated areas are discussed.

  15. Preliminary technology report for Southern Sector bioremediation

    SciTech Connect

    Brigmon, R.L.; White, R.; Hazen, T.C.; Jones, D.; Berry, C.

    1997-06-01

    This project was designed to demonstrate the potential of intrinsic bioremediation and phytoremediation in the Southern Sector of the A/M-Area at the Savannah River Site. A subsurface plume of trichloroethylene (TCE) and perchloroethylene (PCE) is present in the Lost Lake aquifer upgradient of the study site and is predicted to impact the area at some point in the future. The surface area along the Lost lake aquifer seep line where the plume is estimated to emerge was identified. Ten sites along the seep line were selected for biological, chemical, and contaminant treatability analyses. A survey was undertaken in this area to to quantify the microbial and plant population known to be capable of remediating TCE and PCE. The current groundwater quality upgradient and downgradient of the zone of influence was determined. No TCE or PCE was found in the soils or surface water from the area tested at this time. A TCE biodegradation treatability test was done on soil from the 10 selected locations. From an initial exposure of 25 ppm of TCE, eight of the samples biodegraded up to 99.9 percent of all the compound within 6 weeks. This biodegradation of TCE appears to be combination of aerobic and anaerobic microbial activity as intermediates that were detected in the treatability test include vinyl chloride (VC) and the dichloroethenes (DCE) 1,2-cis-dichloroethylene and 1,1-dichloroethylene. The TCE biological treatability studies were combines with microbiological and chemical analyses. The soils were found through immunological analysis with direct fluorescent antibodies (DFA) and microbiological analysis with direct fluorescent antibodies (DFA) and microbiological analysis to have a microbial population of methanotrophic bacteria that utilize the enzyme methane monooxygenase (MMO) and cometabolize TCE.

  16. Biodegradation of individual and multiple chlorinated aliphatic hydrocarbons by methane-oxidizing cultures.

    PubMed Central

    Chang, H L; Alvarez-Cohen, L

    1996-01-01

    The microbial degradation of chlorinated and nonchlorinated methanes, ethanes, and ethanes by a mixed methane-oxidizing culture grown under chemostat and batch conditions is evaluated and compared with that by two pure methanotrophic strains: CAC1 (isolated from the mixed culture) and Methylosinus trichosporium OB3b. With the exception of 1,1-dichloroethylene, the transformation capacity (Tc) for each chlorinated aliphatic hydrocarbon was generally found to be in inverse proportion to its chlorine content within each aliphatic group (i.e., methanes, ethanes, and ethenes), whereas similar trends were not observed for degradation rate constants. Tc trends were similar for all methane-oxidizing cultures tested. None of the cultures were able to degrade the fully chlorinated aliphatics such as perchloroethylene and carbon tetrachloride. Of the four cultures tested, the chemostat-grown mixed culture exhibited the highest Tc for trichloroethylene, cis-1,2-dichloroethylene, tetrachloroethane, 1,1,1-trichloroethane, and 1,2-dichloroethane, whereas the pure batch-grown OB3b culture exhibited the highest Tc for all other compounds tested. The product toxicity of chlorinated aliphatic hydrocarbons in a mixture containing multiple compounds was cumulative and predictable when using parameters measured from the degradation of individual compounds. The Tc for each chlorinated aliphatic hydrocarbon in a mixture (Tcmix) and the total Tc for the mixture (sigma Tcmix) are functions of the individual Tc, the initial substrate concentration (S0), and the first-order rate constant (k/Ks) of each compound in the mixture, indicating the importance of identifying the properties and compositions of all potentially degradable compounds in a contaminant mixture. PMID:8795228

  17. Endocrine disruptors and estrogenic effects on male reproductive axis.

    PubMed

    Sikka, Suresh C; Wang, Run

    2008-01-01

    Endocrine disruptors (e.g., polychlorinated biphenyls [PCBs], dichlorodiphenyl-trichloroethane [DDT], dioxin, and some pesticides) are estrogen-like and anti-androgenic chemicals in the environment. They mimic natural hormones, inhibit the action of hormones, or alter the normal regulatory function of the endocrine system and have potential hazardous effects on male reproductive axis causing infertility. Although testicular and prostate cancers, abnormal sexual development, undescended testis, chronic inflammation, Sertoli-cell-only pattern, hypospadias, altered pituitary and thyroid gland functions are also observed, the available data are insufficient to deduce worldwide conclusions. The development of intra-cytoplasmic sperm injection (ICSI) is beyond doubt the most important recent breakthrough in the treatment of male infertility, but it does not necessarily treat the cause and may inadvertently pass on adverse genetic consequences. Many well-controlled clinical studies and basic scientific discoveries in the physiology, biochemistry, and molecular and cellular biology of the male reproductive system have helped in the identification of greater numbers of men with male factor problems. Newer tools for the detection of Y-chromosome deletions have further strengthened the hypothesis that the decline in male reproductive health and fertility may be related to the presence of certain toxic chemicals in the environment. Thus the etiology, diagnosis, and treatment of male factor infertility remain a real challenge. Clinicians should always attempt to identify the etiology of a possible testicular toxicity, assess the degree of risk to the patient being evaluated for infertility, and initiate a plan to control and prevent exposure to others once an association between occupation/toxicant and infertility has been established. PMID:18087652

  18. Persistent organic pollutants (POPs) in populations of the clam Chione californiensis in coastal lagoons of the Gulf of California.

    PubMed

    Vargas-González, Héctor H; Méndez-Rodríguez, Lía C; García-Hernández, Jaqueline; Mendoza-Salgado, Renato A; Zenteno-Savín, Tania; Arreola-Lizárraga, José A

    2016-07-01

    This study examines the potential public health risk due to the massive use of organochlorine pesticides (OCs) in agriculture in the Gulf of California. Specimens of the clam Chione californiensis were collected from three coastal lagoons (Yavaros, Altata and Reforma). Sites were classified as polluted/nonpolluted based on the presence/absence of OCs as an indicator of the persistence of these pollutants; in polluted sites, the time elapsed since pesticide application (past or recent) was estimated. Screening values (SV) for protecting human health as per the U.S. Environmental Protection Agency (EPA) were used for risk assessment. OCs detected were ranked according to frequency of occurrence as follows: γ-chlordane (75%) > endrin (54%) > aldrin (48%) > heptachlor, and dichlorodiphenyl-trichloroethane (DDE) (37%) > β-heptachlor epoxide (30%) > lindane (α-BHC, δ-BHC) and endosulphan I (≤ 6%). Specifically, OCs detected at the highest concentration were heptachlor in Yavaros (0.0168 µgg(-1)) and Altata (0.0046 µgg(-1)), and aldrin in Reforma (0.0019 µgg(-1)). β-Heptachlor epoxide in Altata and Reforma was the only OC with a concentration exceeding the EPA Screening Value. From our results and based on the monthly consumption limit set forth by EPA, the maximum safe consumption of clams to avoid a carcinogenic risk derived from β-heptachlor epoxide in the fishing villages of Yavaros and Altata is 4 servings per month (1 serving = 0.227 kg) by a 70-kg person. These findings suggest that concentrations of OCs and their isomers in C. californiensis populations reflect environmental persistence as well as recent inputs of OCs into coastal lagoons in the Gulf of California. PMID:27050678

  19. Human health risk assessment of pesticide residues in market-sold vegetables and fish in a northern metropolis of China.

    PubMed

    Fang, Yanyan; Nie, Zhiqiang; Yang, Yanmei; Die, Qingqi; Liu, Feng; He, Jie; Huang, Qifei

    2015-04-01

    With growing concerns about food safety and stricter national standards in China, attention has focused on vegetables and fish as they are an important part of the Chinese daily diet, and pesticide residues can accumulate in these foodstuffs. The local consumption habits of vegetables and fish were determined using questionnaires distributed in the major regions of the northern metropolis. Then, the samples of fruit-like vegetables, leafy and root vegetables, and five species of fish (freshwater and marine) were collected from supermarkets and traditional farmers' markets in the city. The concentrations and profiles of pesticide residues (hexachlorocyclohexane (HCH), dichlorodiphenyl trichloroethane (DDT), and endosulfan) in the samples were determined and compared. For the vegetables, the concentration ranges of ΣDDT, ΣHCH, and Σendosulfan were not detectable (ND) to 10.4 ng/g fresh weight (f.w.), ND to 58.8 ng/g f.w., and ND to 63.9 ng/g f.w., respectively. For the fish samples, the corresponding values were 0.77-25.0 ng/g f.w., 0.02-1.42 ng/g f.w., and 1.22-22.1 ng/g f.w., respectively. Only one celery sample exceeded the maximum residue limits (MRLs) of HCH residues set by Chinese regulations (GB2763-2014). The estimated daily intakes (EDIs) and hazard ratios (HRs) were calculated using data from the recently published Exposure Factors Handbook for the Chinese Population. The EDIs and HRs showed that the levels of organochlorine pesticide (OCP) residues in vegetables and fish in this area are safe. PMID:25395327

  20. Evaluation of indoor residual spray and insecticide treated bed nets in a malaria endemic area of Santhal Pargana, Dumka district (Jharkhand).

    PubMed

    Singh, R K; Das, M K; Dhiman, R C; Mittal, P K; Dua, V K; Sreehari, U; Prasad, Shankar

    2012-09-01

    The study was carried out for evaluation of various activities of malaria control programme in five different tribal and malaria endemic Primary Health Centres of Dumka district (Jharkhand) during 2007-08. A total of 321 houses of 18 villages were surveyed on use of indoor residual spray (IRS) and insecticide-treated bed nets (ITN) and other activities as tool for vector control and interrupting the transmission of malaria. Out of 690 living rooms and 343 verandahs examined, IRS with Dichlorodiphenyl-trichloro-ethane (DDT) was done only in 16.23% living rooms and 64.72% verandahs. Refusal rate of IRS in living rooms was 81.93% due to lack of knowledge regarding the importance of IRS, no prior information to villagers, houses locked, reluctance to remove domestic articles, dislike of smell of DDT spray. Compliance rate of ITN uses was 71.66% during the night, which might be a factor for decline in malaria cases in the study area. Various important components of the programme, viz. surveillance and compliance to treatment activities, use of rapid diagnostic test kits (RDKs), involvement of accredited social health activist (ASHA's) and fever treatment depots (FTDs), laboratory activities, adult mosquito collection, other activities like constitution of village health sanitation committee, information education and communication activities, capacity building, use of larvivorous fishes, supervision of IRS etc. require much strengthening. However, 100% community acceptance was recorded for ITN in the villages surveyed. In addition, an entomological study was carried out for information on prevalence of mosquito species in this area to find out effectiveness of IRS activities. Eleven anopheline species, including three malaria vectors i.e., An. culicifacies, An. stephensi, An. fluviatilis, An. annularis, An. subpictus, An. nigerrimus, An. pallidus, An. aconitus, An. vagus, An. jamsii and An. splendidus were collected from cattle and human dwellings. PMID:25145065

  1. p-Chloro-diphenyl diselenide reverses memory impairment-related to stress caused by corticosterone and modulates hippocampal [(3)H]glutamate uptake in mice.

    PubMed

    Zborowski, Vanessa A; Sari, Marcel H M; Heck, Suélen O; Stangherlin, Eluza C; Neto, José S S; Nogueira, Cristina W; Zeni, Gilson

    2016-10-01

    Chronic stress or chronically high levels of glucocorticoids can result in memory impairment. This study aimed to investigate if 4,4'-dichloro-diphenyl diselenide (p-ClPhSe)2 reverses memory impairment-related to stress caused by corticosterone administration in mice and its possible mechanism of action. Swiss mice received corticosterone (20μg/ml) in their drinking water during four weeks. In the last week, the animals were treated with (p-ClPhSe)2 (1 or 5mg/kg) by the intragastric route (i.g.) once a day for 7days. The cognitive performance of mice was assessed through the object recognition test (ORT), the object location test (OLT) and the step-down passive avoidance test (SDPA), some of predictive tests of memory. Biochemical parameters were determined and locomotor activity of mouse was performed to gain insight in (p-ClPhSe)2 toxicity. The findings demonstrated that treatment with (p-ClPhSe)2 in both doses was effective in reversing memory deficits in the ORT, the OLT and the SDPA caused by corticosterone exposure in mice. Treatment with (p-ClPhSe)2 at both doses reversed the increase in the [(3)H] glutamate uptake by hippocampal slices of mice treated with corticosterone. By contrast, [(3)H] glutamate uptake by brain cortical slices was not altered in mice exposed to corticosterone. The Na(+)K(+)ATPase activity was not altered in hippocampus and cerebral cortices of mice treated with corticosterone. There was no sign of toxicity in mice treated with (p-ClPhSe)2. This organoselenium compound reversed memory impairment-related to stress caused by corticosterone and modulated hippocampal [(3)H]glutamate uptake in mice. PMID:27211333

  2. Spatial and temporal variation of PCBs and organochlorine pesticides in the Antarctic minke whales, Balaenoptera bonaerensis, in the period 1987-2005.

    PubMed

    Yasunaga, Genta; Fujise, Yoshihiro; Zenitani, Ryoko; Tanabe, Shinsuke; Kato, Hidehiro

    2015-05-01

    Concentrations of polychlorinated biphenyls (PCBs), dichlorodiphenyl trichloroethane and its metabolites (DDTs), hexachlorocyclohexane isomers (HCHs), hexachlorobenzene (HCB) and chlordane compounds (CHLs) were determined in the blubber of males (20-25 years old) of Antarctic minke whales, Balaenoptera bonaerensis, from the International Whaling Commission (IWC) management Areas IV (70°-130°E) and V (130°E-170°W), south 60°S. The ranges of concentrations (ng g(-1) lipid wt.) for each compound were, PCBs: 7.7-89; DDTs: 29-340; HCHs: 0.20-4.3; HCB: 75-430; CHLs: 10-120, which were much lower than those in common minke whales, Balaenoptera acutorostrata, from the northern hemisphere. The levels of PCBs, HCHs, HCB and CHLs in Area IV were significantly higher than those in Area V, while the levels of DDTs in both areas were similar. For comparing the fate among four pesticides in the Antarctic Ocean avoiding the effect of variance due to food intake, the ratios of the pesticides to PCBs, which has an extremely high chemical stability and environmental persistence, were examined. The HCHs/PCBs ratio decreased by a factor of about 20 in a span of 16 years in both Areas IV and V, while temporal trends of DDTs/PCBs, HCB/PCBs and CHLs/PCBs ratios were not observed. These results indicate that PCBs, DDTs, HCB and CHLs levels did not vary or slightly decreased in Areas IV and V during the study period. However HCHs levels clearly decreased. Spatial differences seems to be related to differences in food intake among whales, and temporal differences seems to be related to the length stay of OCs in the Antarctic Ocean. PMID:25637712

  3. Temporal trends of contaminants in cod from Icelandic waters.

    PubMed

    Sturludottir, Erla; Gunnlaugsdottir, Helga; Jorundsdottir, Hronn O; Magnusdottir, Elin V; Olafsdottir, Kristin; Stefansson, Gunnar

    2014-04-01

    Contaminants have been analyzed in cod (Gadus morhua) since 1990 as part of the national monitoring program for the environmental conditions in the sea around Iceland. The aim of this study was to determine the temporal trends of persistent organic pollutants (POPs: polychlorinated biphenyls (PCBs), p,p'-dichlorodiphenyl dichloroethene (p,p'-DDE), hexachlorobenzene (HCB), hexachlorocyclohexanes (HCHs), chlordanes (CHLs) and toxaphenes (Tox)) and trace elements (As, Cd, Cu, Hg, Pb, Se and Zn) in cod over the last two decades at two different locations in the Arctic Ocean north of Iceland. The relationship between the contaminant concentrations and biological covariates was also determined. All of the POPs showed decreasing trends but the trace elements showed no clear signs of trend except arsenic which showed an increasing trend and zinc which showed a decreasing trend. The concentration of the POPs were lower or similar in the Icelandic cod compared to cod sampled in Norway, the Barents Sea and in the Baltic Sea, except for HCB which was higher in the Icelandic cod compared to the Norwegian cod. The concentration of the trace elements As, Cu, Hg and Zn were similar in the Icelandic cod compared to cod sampled in Norway and Greenland but the concentration of Cd was higher in the Icelandic cod. The inclusion of the biological covariates was found to be important for the statistical analysis. The POPs had a positive relationship with liver fat content but negative relationship with liver weight. The trace elements had a negative relationship with liver fat and liver weight except As which had positive relationship with liver weight. Only positive relationships were observed between the contaminant concentrations and length. PMID:24463254

  4. Multiresidue pesticide analysis of ginseng powders using acetonitrile- or acetone-based extraction, solid-phase extraction cleanup, and gas chromatography-mass spectrometry/selective ion monitoring (GC-MS/SIM) or -tandem mass spectrometry (GC-MS/MS).

    PubMed

    Wong, Jon W; Zhang, Kai; Tech, Katherine; Hayward, Douglas G; Krynitsky, Alexander J; Cassias, Irene; Schenck, Frank J; Banerjee, Kaushik; Dasgupta, Soma; Brown, Don

    2010-05-26

    A multiresidue method for the analysis of 168 pesticides in dried powdered ginseng has been developed using acetonitrile or acetone mixture (acetone/cyclohexane/ethyl acetate, 2:1:1 v/v/v) extraction, solid-phase extraction (SPE) cleanup with octyl-bonded silica (C(8)), graphitized carbon black/primary-secondary amine (GCB/PSA) sorbents and toluene, and capillary gas chromatography-mass spectrometry/selective ion monitoring (GC-MS/SIM) or -tandem mass spectrometry (GC-MS/MS). The geometric mean limits of quantitation (LOQs) were 53 and 6 microg/kg for the acetonitrile extraction and 48 and 7 microg/kg for the acetone-based extraction for GC-MS/SIM and GC-MS/MS, respectively. Mean percent recoveries and standard deviations from the ginseng fortified at 25, 100, and 500 microg/kg using GC-MS/SIM were 87 +/- 10, 88 +/- 8, and 86 +/- 10% from acetonitrile extracts and 88 +/- 13, 88 +/- 12, and 88 +/- 14% from acetone mixture extracts, respectively. The mean percent recoveries from the ginseng at the 25, 100, and 500 microg/kg levels using GC-MS/MS were 83 +/- 19, 90 +/- 13, and 89 +/- 11% from acetonitrile extracts and 98 +/- 20, 91 +/- 13, and 88 +/- 14% from acetone extracts, respectively. Twelve dried ginseng products were found to contain one or more of the following pesticides and their metabolites: BHCs (benzene hexachlorides, alpha-, beta-, gamma-, and delta-), chlorothalonil, chlorpyrifos, DDT (dichlorodiphenyl trichloroethane), dacthal, diazinon, iprodione, quintozene, and procymidone ranging from <1 to >4000 microg/kg. No significant differences were found between the two extraction solvents, and GC-MS/MS was found to be more specific and sensitive than GC-MS/SIM. The procedures described were shown to be effective in screening, identifying, confirming, and quantitating pesticides in commercial ginseng products. PMID:20225896

  5. Determinants of polychlorinated biphenyls (PCBs) in the sera of mothers and children from Michigan farms with PCB-contaminated silos

    SciTech Connect

    Schantz, S.L.; Jacobson, J.L.; Jacobson, S.W.; Humphrey, H.E.B.; Welch, R.; Gasior, D.

    1994-11-01

    Blood samples were collected from 28 mothers and from 38 school-aged children from Michigan farms on which there were polychlorinated biphenyl (PCB)-contaminated silos. The samples were analyzed for PCBs and other contaminants, including polybrominated biphenyls (PBBs) and dichlorodiphenyl trichloroethane (p,p{prime}-DDT + p,p{prime}-DDE) via packed column gas chromatography. The PCBs were quantified, using the Webb-McCall method, with Aroclors 1016 and 1260 used as reference standards. Approximately 42% of the children had serum PCB levels above the detection limit of 3.0 ng/ml. The values ranged from 3.1 to 23.3 ng/ml, with a mean of 6.8 ng/ml. In contrast, PCBs were detected in 86% of the mothers. The mean serum concentration was somewhat higher for the mothers (9.6 ng/ml), but the range was similar to that found for the children. PBBs were not detected in any of the children, but were present in trace amounts in 25% of the mothers. Conversely, DDT was present in 66% of the children and 93% of the mothers. As with PCBs, DDT concentrations were somewhat higher in the mothers. DDE accounted for 89% of the total DDT in serum. Various potential sources of exposure were evaluated as possible determinants of serum PCB levels, using hierarchical multiple regression. Years of residence on a silo farm and consumption of PCB-contaminated Great Lakes fish both accounted for significant portions of the variance in maternal serum PCB levels. Exposure via breast-feeding explained a large and highly significant proportion of the variance in the children`s serum PCB concentrations, suggesting that breast milk was the primary source of PCB exposure for these children. Years of residence on a silo farm also explained a significant proportion of the variance in children`s serum PCBs. 29 refs., 1 fig., 5 tabs.

  6. Year 5 Post-Remediation Biomonitoring of Pesticides and other Contaminants in Marine Waters near the United Heckathorn Superfund Site, Richmond, California

    SciTech Connect

    Kohn, Nancy P.; Kropp, Roy K.

    2002-08-01

    Marine sediment remediation at the United Heckathorn Superfund Site in Richmond, California, was completed in April 1997. The Record of Decision included a requirement for five years of post-remediation monitoring be conducted in the waterways near the site. The present monitoring year, 2001? 2002, is the fifth and possibly final year of post-remediation monitoring. In March 2002, water and mussel tissues were collected from the four stations in and near Lauritzen Channel that have been routinely monitored since 1997-98. A fifth station in Parr Canal was sampled in Year 5 to document post-remediation water and tissue concentrations there. Dieldrin and dichlorodiphenyl trichloroethane (DDT) were analyzed in water samples and in tissue samples from resident (i.e., naturally occurring) mussels. As in Years 3 and 4, mussels were not transplanted to the study area in Year 5. Year 5 concentrations of dieldrin and total DDT in water and total DDT in tissue were compared with those from Years 1 through 4 of post-remediation monitoring, and with preremediation data from the California State Mussel Watch Program and the Ecological Risk Assessment for the United Heckathorn Superfund Site. Year 5 water samples and mussel tissues were also analyzed for polychlorinated biphenyls (PCB), which were detected in sediment samples during Year 2 monitoring and were added to the water and mussel tissue analyses in 1999. Contaminants of concern in Year 5 water samples were analyzed in both bulk (total) phase and dissolved phase, as were total suspended solids, to evaluate the contribution of particulates to the total contaminant concentration.

  7. Post-Remediation Biomonitoring of Pesticides and Other Contaminants in Marine Waters and Sediment Near the United Heckathorn Superfund Site, Richmond, California

    SciTech Connect

    LD Antrim; NP Kohn

    2000-09-06

    This report, PNNL-1 3059 Rev. 1, was published in July 2000 and replaces PNNL-1 3059 which is dated October 1999. The revision corrects tissue concentration units that were reported as dry weight but were actually wet weight, and updates conclusions based on the correct reporting units. Marine sediment remediation at the United Heckathorn Superfund Site was completed in April 1997. Water and mussel tissues were sampled in February 1999 from four stations near Lauritzen Canal in Richmond, California, for Year 2 of post-remediation monitoring of marine areas near the United Heckathom Site. Dieldrin and dichlorodiphenyl trichloroethane (DDT) were analyzed in water samples, tissue samples from resident mussels, and tissue samples from transplanted mussels deployed for 4 months. Concentrations of dieldrin and total DDT in water and total DDT in tissue were compared with Year 1 of post-remediation monitoring, and with preremediation data from the California State Mussel Watch program (tissue s) and the Ecological Risk Assessment for the United Heckathorn Superfund Site (tissues and water). Mussel tissues were also analyzed for polychlorinated biphenyls (PCB), which were detected in sediment samples. Chlorinated pesticide concentrations in water samples were similar to preremediation levels and did not meet remediation goals. Mean dieldrin concentrations in water ranged from 0.62 ng/L to 12.5 ng/L and were higher than the remediation goal (0.14 ng/L) at all stations. Mean total DDT concentrations in water ranged from 14.4 ng/L to 62.3 ng/L and exceeded the remediation goal (0.59 ng/L) at all stations. The highest concentrations of both DDT and dieldrin were found at the Lauritzen Canal/End station. Despite exceedence of the remediation goals, chlorinated pesticide concentrations in Lauritzen Canal water samples were notably lower in 1999 than in 1998. PCBS were not detected in water samples in 1999.

  8. Effects of age, sex, and persistent organic pollutants on DNA methylation in children

    PubMed Central

    Huen, Karen; Yousefi, Paul; Bradman, Asa; Yan, Liying; Harley, Kim G.; Kogut, Katherine; Eskenazi, Brenda; Holland, Nina

    2015-01-01

    Epigenetic changes such as DNA methylation may be a molecular mechanism through which environmental exposures affect health. Methylation of Alu and long interspersed nucleotide elements (LINE-1) is a well-established measure of DNA methylation often used in epidemiologic studies. Yet, few studies have examined the effects of host factors on LINE-1 and Alu methylation in children. We characterized the relationship of age, sex, and prenatal exposure to persistent organic pollutants (POPs), dichlorodiphenyl trichloroethane (DDT), dichlorodiphenyldichloroethylene (DDE), and polybrominated diphenyl ethers (PBDEs), with DNA methylation in a birth cohort of Mexican-American children participating in the CHAMACOS study. We measured Alu and LINE-1 methylation by pyrosequencing bisulfite-treated DNA isolated from whole blood samples collected from newborns and 9-year old children (n=358). POPs were measured in maternal serum during late pregnancy. Levels of DNA methylation were lower in 9-year olds compared to newborns and were higher in boys compared to girls. Higher prenatal DDT/E exposure was associated with lower Alu methylation at birth, particularly after adjusting for cell type composition (p=0.02 for o,p′ -DDT). Associations of POPs with LINE-1 methylation were only identified after examining the co-exposure of DDT/E with PBDEs simultaneously. Our data suggest that repeat element methylation can be an informative marker of epigenetic differences by age and sex and that prenatal exposure to POPs may be linked to hypomethylation in fetal blood. Accounting for co-exposure to different types of chemicals and adjusting for blood cell types may increase sensitivity of epigenetic analyses for epidemiological studies. PMID:24375655

  9. Segmented tetrasulfonated copoly(arylene ether sulfone)s: improving proton transport properties by extending the ionic sequence.

    PubMed

    Takamuku, Shogo; Weiber, E Annika; Jannasch, Patric

    2013-02-01

    The morphologies and proton-transport efficiencies of segmented copoly(arylene ether sulfone) ionomers that contain tetrasulfonated sequences are compared with the corresponding copolymers with disulfonated sequences. Tetrasulfonated 4,4'-bis[(4-chlorophenyl)sulfonyl]-1,1'-biphenyl (sBCPSBP) is synthesized by metalation and sulfination. This new monomer is then used in K(2)CO(3)-mediated polycondensations of mixtures with 4,4'-dichlorodiphenyl sulfone (DCDPS) and 4,4'-dihydroxybiphenyl in dimethyl sulfoxide at 110 °C to prepare segmented copolymers with tetrasulfonated units. The corresponding disulfonated copolymers are prepared by using disulfonated DCDPS instead of sBCPSBP. Small-angle X-ray scattering measurements of the fully aromatic copolymer membranes show ionomer peaks that indicate significantly larger characteristic separation lengths of the tetrasulfonated copolymers compared to those of the corresponding disulfonated copolymers with similar ionic contents. This implies a much more efficient phase separation of the ionic groups in the segmented tetrasulfonated copolymer membranes, especially at low-to-medium ionic contents. The enhanced phase separation has a pronounced positive effect on water uptake characteristics and proton transport properties. Under a reduced relative humidity (RH), the tetrasulfonated copolymer membranes show a significantly higher conductivity than the disulfonated ones, particularly at low-to-medium ionic contents. At an ion-exchange capacity of 1 meq g(-1), the conductivity of the tetrasulfonated copolymer membrane at 30 % RH is higher than that of the disulfonated membrane at 90 % RH. Because of their relative ease of synthesis, segmented copolymers based on well-designed multisulfonated monomers may provide a viable alternative to the more complex sulfonated block and graft copolymers for use as fuel-cell membranes. PMID:23307760

  10. Synthesis and fuel cell characterization of blend membranes from phenyl phosphine oxide containing flourinated novel polymers

    NASA Astrophysics Data System (ADS)

    Gürtekin Seden, Merve; Baştürk, Emre; Inan, Tülay Y.; Kayaman Apohan, Nilhan; Güngör, Atilla

    2014-12-01

    Novel fluorinated poly(arylene ether)'s are synthesized from polycondensation of bis (p-hydroxy-tetrafluoro) phenyl) phenyl phosphine oxide (PFPPO-OH) with 4,4‧-dichlorodiphenyl sulfone (DCDPS) and 2,2-bis(4-hydroxyphenyl)propane (Bisfenol A) (Copolymer 1a) or 2,2-bis(4-hydroxyphenyl) hexafluoropropane (Bisphenol AF) (Copolymer 1b). The fluorinated copolymers have been blended with sulphonated poly(ether ether ketone)-SPEEK by solvent casting method. The water uptake and proton conductivity of the blend membranes decreases with the increase of copolymer content as expected, but proton conductivity values are still comparable to that of Nafion117® membrane. Addition of hydrophobic copolymer 1b to the SPEEK caused increase in water vapor transmission. Methanol permeability of the membranes is decreased to 8.2 × 10-8 cm2 s-1 and 1.3 × 10-9 cm2 s-1 by addition of Copolymer 1a and 1b, respectively and they are much lower than that of Nafion® 117 (1.21E-06 (cm2 s-1). The blend membranes endure up to 6.5 h before it starts to dissolve. Hydrogen and oxygen permeability of the blend membranes is one-hundredth of the Nafion®. Fluorinated polymer improved chemical, mechanical, and hydrolytic stability and also phenyl phosphine oxide structure in the ionomer increased the thermal stability, gas and methanol permeability and overcomed the drawbacks of the Nafion® type membranes.

  11. Impairments of memory and learning in older adults exposed to polychlorinated biphenyls via consumption of Great Lakes fish.

    PubMed Central

    Schantz, S L; Gasior, D M; Polverejan, E; McCaffrey, R J; Sweeney, A M; Humphrey, H E; Gardiner, J C

    2001-01-01

    An association between in utero polychlorinated biphenyl (PCB) exposure and impaired childhood intellectual functioning has been reported, but the potential impact of PCB exposure during adulthood on intellectual functioning has received little attention. We assessed the impact of PCBs and other fish-borne contaminants on intellectual functioning in older adults. The subjects were 49- to 86-year-old Michigan residents recruited from an existing cohort. Fish eaters ate > 24 lb of sport-caught Lake Michigan fish per year and non-fish eaters ate < 6 lb of Lake Michigan fish per year. A battery of cognitive tests including tests of memory and learning, executive function, and visual-spatial function was administered to 180 subjects (101 fish eaters and 79 non-fish eaters). Blood samples were analyzed for PCBs and 10 other contaminants. We evaluated cognitive outcomes using multiple regression. PCBs and dichlorodiphenyl dichloroethene (DDE) were markedly elevated in fish eaters. After controlling for potential confounders PCB, but not DDE, exposure was associated with lower scores on several measures of memory and learning. These included the Weschler Memory Scale verbal delayed recall (p = 0.001), the semantic cluster ratio (p = 0.006), and list A, trial 1 (p = 0.037), from the California Verbal Learning Test. In contrast, executive and visual-spatial function were not impaired by exposure to either PCBs or DDE. In conclusion, PCB exposure during adulthood was associated with impairments in memory and learning, whereas executive and visual-spatial function were unaffected. These results are consistent with previous research showing an association between in utero PCB exposure and impairments of memory during infancy and childhood. PMID:11445515

  12. Online analysis of chlorine stable isotopes in chlorinated ethylenes: an inter-laboratory study

    NASA Astrophysics Data System (ADS)

    Bernstein, Anat; Shouakar-Stash, Orfan; Hunkeler, Daniel; Sakaguchi-Söder, Kaori; Laskov, Christine; Aravena, Ramon; Elsner, Martin

    2010-05-01

    In the last decade, compound-specific stable isotopes analysis of groundwater pollutants became an important tool to identify different sources of the same pollutant and for tracking natural attenuating processes in the sub-surface. It has been shown that trends in the isotopic composition of the target compounds can shed light on in-situ processes that are otherwise difficult to track. Analytical methods of carbon, nitrogen and hydrogen were established and are by now frequently used for a variety of organic pollutants. Yet, the motivation of introducing analytical methods for new isotopes is emerging. This motivation is further enhanced, as advantages of using two or more stable isotopes for gaining better insight on degradation pathways are well accepted. One important element which demands the development of appropriate analytical methods is chlorine, which is found in various groups of organic pollutants, among them the chlorinated ethylenes. Chlorinated ethylenes are considered as high priority environmental pollutants, and the development of suitable chlorine isotope methods for this group of pollutants is highly desired. Ideally, stable isotope techniques should have the capability to determine the isotopic composition of and individual target compound in a non-pure mixture, without the requirement of a laborious off-line treatment. Indeed, in the last years two different concepts for on-line chlorine isotope analysis methods were introduced, by using either a standard quadrapole GC/MS (Sakaguchi-Söder et al., 2007) or by using a GC/IRMS (Shouakar-Stash et al., 2006). We present a comparison of the performances of two concepts, carried out in five different laboratories: Waterloo (GC/IRMS), Neuchâtel (GC/MS), Darmstadt (GC/MS), Tübingen (GC/MS) and Munich (GC/IRMS). This comparison was performed on pure trichloroethylene and dichloroethylene products of different manufactures, as well as trichloroethylene and dichloroethylene samples that were exposed to

  13. Inorganic and organic ground-water chemistry in the Canal Creek area of Aberdeen Proving Ground, Maryland

    USGS Publications Warehouse

    Lorah, M.M.; Vroblesky, D.A.

    1989-01-01

    Groundwater chemical data were collected from November 1986 through April 1987 in the first phase of a 5-year study to assess the possibility of groundwater contamination in the Canal Creek area of Aberdeen Proving Ground, Maryland. Water samples were collected from 87 observation wells screened in Coastal Plain sediments; 59 samples were collected from the Canal Creek aquifer, 18 from the overlying surficial aquifer, and 10 from the lower confined aquifer. Dissolved solids, chloride, iron, manganese, fluoride, mercury, and chromium are present in concentrations that exceed the Federal maximum contaminant levels for drinking water. Elevated chloride and dissolved-solids concentrations appear to be related from contaminant plumes but also could result from brackish-water intrusion. Excessive concentrations of iron and manganese were the most extensive water quality problems found among the inorganic constituents and are derived from natural dissolution of minerals and oxide coatings in the aquifer sediments. Volatile organic compounds are present in the Canal Creek and surficial aquifers, but samples from the lower confined aquifer do not show any evidence of contamination by inorganic or organic chemicals. The volatile organic contaminants detected in the groundwater and their maximum concentrations (in micrograms/L) include 1,1,2,2- tetrachloroethane (9,000); carbon tetrachloride (480); chloroform (460); 1,1,2-trichloroethane (80); 1,2-dichloroethane (990); 1,1-dichloroethane (3.1); tetrachloroethylene (100); trichloroethylene (1,800); 1,2-trans- dichloroethylene (1,200); 1,1-dichloroethylene (4.4); vinyl chloride (140); benzene (70); and chlorobenzene (39). On the basis of information on past activities in the study area, some sources of the volatile organic compounds include: (1) decontaminants and degreasers; (2) clothing-impregnating operations; (3) the manufacture of impregnite material; (4) the manufacture of tear gas; and (5) fuels used in garages and at

  14. Concentration of organochlorines in human brain, liver, and adipose tissue autopsy samples from Greenland.

    PubMed Central

    Dewailly, E; Mulvad, G; Pedersen, H S; Ayotte, P; Demers, A; Weber, J P; Hansen, J C

    1999-01-01

    Organochlorines are persistent lipophilic compounds that accumulate in Inuit people living in circumpolar countries. Organochlorines accumulate as a result of the Inuits' large consumption of sea mammal fat; however, available data are limited to blood lipids, milk fat, and adipose tissue. We report results of organochlorine determination in liver, brain, omental fat, and subcutaneous abdominal fat samples collected from deceased Greenlanders between 1992 and 1994. Eleven chlorinated pesticides and 14 polychlorinated biphenyl congeners were measured in tissue lipid extracts by high-resolution gas chromatography with electron capture detection. Mean concentrations of polychlorinated biphenyls, 2, 2'-bis(4-chlorophenyl)-1,1-dichloroethylene, ss-hexachlorocyclohexane, hexachlorobenzene, mirex, trans-nonachlor, and oxychlordane in adipose tissue samples from Greenlanders were 3-34-fold higher than those measured using the same analytical method in samples from Canadians in Quebec City, Quebec. Brain lipids contained lower concentrations of all organochlorines than lipids extracted from other tissues. Organochlorine residue levels in lipid extracts from liver, omental fat, and subcutaneous abdominal fat samples were similar, with the exception of ss-hexachlorocyclohexane, which reached a greater concentration in liver lipids than in lipids from both adipose tissues (4-fold; p < 0. 05). Comparisons with available international data on adipose tissue levels reveal that the organochlorine body burden in the Inuit population of Greenland is presently among the highest resulting from environmental exposure. Images Figure 1 PMID:10504150

  15. Water quality in the Withers Swash Basin, with emphasis on enteric bacteria, Myrtle Beach, South Carolina, 1991-93

    USGS Publications Warehouse

    Guimaraes, W.B.

    1995-01-01

    Water samples were collected in 1991-93 from Withers Swash and its two tributaries (the Mainstem and KOA Branches) in Myrtle Beach, S.C., and analyzed for physical properties, organic and inorganic constituents, and fecal coliform and streptococcus bacteria. Samples were collected during wet- and dry-weather conditions to assess the water quality of the streams before and after storm runoff. Water samples were analyzed for over 200 separate physical, chemical, and biological constituents. Concentrations of 11 constituents violated State criteria for shellfish harvesting waters, and State Human Health Criteria. The 11 constituents included concentrations of dissolved oxygen, arsenic, lead, cadmium, mercury, chlordane, dieldrin, 1,1,1-trichloroethane, 1,1-dichloroethylene, trichloroethylene, and fecal coliform bacteria. Water samples were examined for the presence of enteric bacteria (fecal coliform and fecal streptococcus) at 46 sites throughout the Withers Swash Basin and 5 sites on the beach and in the Atlantic Ocean. Water samples were collected just upstream from all confluences in order to determine sources of bacterial contamination. Temporally and spatially high concentrations of enteric bacteria were detected throughout the Withers Swash Basin; however, these sporadic bacteria concentrations made it difficult to determine a single source of the contamination. These enteric bacteria concentrations are probably derived from a number of sources in the basin including septic tanks, garbage containers, and the feces of waterfowl and domestic animals.

  16. Chlorinated aliphatic and aromatic VOC decomposition in air mixture by using electron beam irradiation

    NASA Astrophysics Data System (ADS)

    Chmielewski, A. G.; Sun, Yong-Xia; Bułka, S.; Zimek, Z.

    2004-09-01

    Chlorinated aliphatic and aromatic hydrocarbons, which are emitted from coal power station and waste incinerators, are very harmful to the environment and human health. Recent studies show that chlorinated aliphatic and aromatic hydrocarbons are suspected to be the precursors of dioxin's formation. Dioxin's emission into atmosphere will cause severe environmental problems by ecology contamination. l,4-dichlorobenzene(l,4-DCB) and cis-dichloroethylene( cis-DCE) were chosen as representative chlorinated aromatic and aliphatic compounds, respectively. Their decomposition was investigated by electron beam irradiation. The experiments were carried out "in batch" system. It is found that over 97% cis-DCE is decomposed having an initial concentration of 661 ppm. G-values of cis-DCE decomposition vary from 10 to 28 (molecules/100 eV) for initial concentration of 270-1530 ppm cis-DCE. The decomposition is mainly caused by secondary electron attachment and Cl addition reactions. Comparing with cis-DCE, 1,4-DCB decomposition needs higher absorbed dose. G-value of 1,4-DCB is below 4 molecules/100 eV.

  17. Organochlorine pesticides, PCBs, dioxins, and metals in postterm peregrine falcon (Falco peregrinus) eggs from the Mid-Atlantic states, 1993-1999.

    PubMed

    Clark, Kathleen E; Zhao, Yuan; Kane, Cynthia M

    2009-07-01

    Peregrine falcons were extirpated from the eastern United States by 1964 due to the effects of dichloro-diphenyl-trichlorethane (DDT) (Peakall and Kiff 1988). As a result of restoration efforts, peregrines have largely recovered in the region but remain a barometer of environmental contamination. In the course of monitoring nests, biologists in the mid-Atlantic states collected peregrine falcon eggs that failed to hatch. In the period 1993-1999, 93 eggs were collected from 66 nests in 31 locations in New Jersey, Pennsylvania, Delaware, Maryland, and Virginia. We analyzed eggs for organochlorine pesticides, PCBs, and metals, and calculated toxic equivalencies (TEQs) for dioxins and furans. Organochlorine contaminants were detected in eggs from all parts of the region. Although nest success in all parts of the region was good, the PCB TEQ in the Atlantic-New Jersey region was significantly related to nest success, and the regionwide PCB TEQ was nearly significant for nest success across the five-state area. dichloro-diphenyl-dichloroethylene (DDE), DDT, and total PCBs were negatively correlated with eggshell thickness, although eggshell thinning (10.4%) was not at a level associated with deleterious population effects. The five states represented in this study are productive for peregrine falcons and have contributed to the recovery of this species. However, the results suggest that Atlantic coastal peregrines might be subject to contaminant burdens that have the potential to decrease nest success and productivity. PMID:18853082

  18. Bioremediation of Trichloroethylene-Contaminated Sediments Augmented with a Dehalococcoides Consortia

    SciTech Connect

    McKinsey, P.C.

    2003-02-20

    At the Department of Energy's (DOE) Savannah River Site (SRS) in Aiken, SC there are a number of sites contaminated with Chlorinated Ethenes (CE) due to past disposal practices. Sediments from two CE contaminated SRS locations were evaluated for trichloroethylene (TCE) biodegradation through anaerobic laboratory microcosms. The testing included addition of amendments and bioaugmentation of sediments. The anaerobic microcosms were first amended with substrates including acetate, lactate, molasses, soybean oil, methanol, sulfate, yeast extract, Regenesis HRC(R), and MEAL (methanol, ethanol, acetate, lactate mixture). Microcosms were analyzed after biostimulation for 9 months and no significant TCE biodegradation was observed. At 10 months, additional TCE, fresh amendments, and a mixed culture containing Dehalococcoides ethenogenes were added to active microcosms. A significant decrease in TCE concentrations and an increase in biodegradation products cis-dichloroethylene (cDCE) and vinyl chloride (VC) were noted within 2 weeks of bioaugmentation. Microcosms amended with lactate and sulfate showed complete transformation of TCE (3 ppm) to ethene within 40 days after bioaugmentation. Microcosms amended with other substrates - soybean oil, acetate, yeast extract, and methanol - also show enhanced biodegradation of TCE to ethene. Microcosms amended with molasses and Regenesis HRC showed limited TCE transformation. No TCE transformation was seen in killed control microcosms. On the basis of these successful results, plans are underway for field-scale in-situ deployment of biostimulation/bioaugmentation at SRS.

  19. Damage to hepatic cellular membranes by chlorinated olefins with emphasis on synergism and antagonism.

    PubMed Central

    Reynolds, E S; Moslen, M T

    1977-01-01

    The fundamental reactivity or stability of the chloroethylene molecules affects their hepatotoxic potential. Extent and symmetry of the chlorine substitution, which alters electron delocalization, charge polarization, and solubility, affect biologic response. The most nonsymmetrically depolarized chloroethylene, 1,1-dichloroethylene (1,1-DCE) is the most hepatotoxic and causes a unique pattern of hepatocellular injury involving mitochondria, plasma membranes, and chromatin. The injury caused by the other chloroethylenes examined appears to profoundly affect the structural integrity of the endoplasmic reticulum with toxic potential in the order: trichloroethylene (TRI) greater than vinyl chloride (VCM) greater than perchloroethylene (PER). Pretreatments which increased cytochrome P-450 contents, thus presumably augmenting metabolic activation to a reactive intermediate such as an epoxide, enhanced or were synergistic to the hepatotoxic potential of TRI, VCM and PER but were protective or antagonistic to 1,1-DCE hepatotoxicity. Biologic response to 1,1-DCE may be expressed by a different metabolic pathway. Glutathione appears to be involved in the biologic response to all nonsymmetric chloroethylenes and toact as an antagonist against injury. Marked differences in the patterns of injury and the biologic responses suggest that more than one mechanism is involved in the production of injury by chloroethylenes. Images FIGURE 3. FIGURE 4. PMID:612438

  20. Relationship between Dehalococcoides DNA in ground water and rates of reductive dechlorination at field scale.

    PubMed

    Lu, Xiaoxia; Wilson, John T; Kampbell, Donald H

    2006-09-01

    Certain strains of Dehalococcoides bacteria can dechlorinate chlorinated ethylenes to harmless products. This study was conducted to determine if there is a valid association between the density of Dehalococcoides DNA in ground water and the observed rates of reductive dechlorination at field scale. Dehalococcoides DNA in water from monitoring wells was determined using the quantitative real time polymerase chain reaction (q-PCR) with DNA primer set specific for Dehalococcoides organisms. Dechlorination rate constants were extracted from field data using the BIOCHLOR software. Of the six conventional plumes surveyed, "generally useful" rates of dechlorination (greater than or equal to 0.3 per year) of cis-dichloroethylene (cis-DCE) and vinyl chloride (VC) along the flow path were observed at three sites where Dehalococcoides DNA was detected, and little attenuation of cis-DCE and VC occurred at two sites where Dehalococcoides DNA was not detected. At the two sites where there was no net direction of ground water flow, the relationship between the density of Dehalococcoides DNA in ground water and the trend in concentrations of chlorinated ethylenes over time in monitoring wells was not so consistent as that observed for the conventional plumes. A comparison of our study to a field study performed by Lendvay and his coworker indicated that monitoring wells did not efficiently sample the Dehalococcoides organisms in the aquifer. PMID:16889813

  1. Chlorinated organic compounds in ground water at Roosevelt Field, Nassau County, Long Island, New York

    USGS Publications Warehouse

    Eckhardt, D.A.; Pearsall, K.A.

    1989-01-01

    Trichloroethylene (TCE), 1,2-dichloroethylene (DCE), and tetrachloroethylene (PCE) have been detected in water from five public-supply wells and six cooling-water wells that tap the Magothy aquifer at Roosevelt Field, a 200-acre area that is now a large shopping mall and office-building complex. The cooling water is discharged after use to the water table (upper glacial) aquifer through a nearby recharge basin and a subsurface drain field. Three plumes of TCE in groundwater have been delineated--the source plume, which has penetrated both aquifers , and two more recent plumes emanating from the two discharge sites in the water-table aquifer. Concentrations of inorganic constituents in the three plumes are the same as those in ambient water in the area. The two secondary plumes discharged cooling water extended at least 1,000 ft south-southeastward in the direction of regional groundwater flow. Pumping at wells screened in the middle and basal sections of the Magothy aquifers, where clay layers are absent and sandy zones provide good vertical hydraulic connection within the aquifer system, has increased the rate of downward contaminant advection. The transient increases in downward movement are cumulative over time and have brought TCE to the bottom of the Magothy aquifer, 500 ft below land surface. (USGS)

  2. Sanitary landfill groundwater monitoring report. Fourth quarter 1996 and 1996 summary

    SciTech Connect

    1997-02-01

    A maximum of eighty-nine wells of the LFW series monitor groundwater quality in the Steed Pond Aquifer (Water Table) beneath the Sanitary Landfill at the Savannah River Site (SRS). These wells are sampled quarterly to comply with the South Carolina Department of Health and Environmental Control Domestic Waste Permit DWP-087A and as part of the SRS Groundwater Monitoring Program. Dichloromethane, a common laboratory contaminant, and chloroethene (vinyl chloride) were the most widespread constituents exceeding standards during 1996. Benzene, trichloroethylene, 1,4-dichlorobenzene, 1,1-dichloroethylene, lead (total recoverable), gross alpha, mercury (total recoverable), tetrachloroethylene, fluoride, thallium, radium-226, radium-228, and tritium also exceeded standards in one or more wells. The groundwater flow direction in the Steed Pond Aquifer (Water Table) beneath the Sanitary Landfill was to the southeast (universal transverse Mercator coordinates). The flow rate in this unit was approximately 141 ft/year during first quarter 1996 and 132 ft/year during fourth quarter 1996

  3. Relation between land use and ground-water quality in the upper glacial aquifer in Nassau and Suffolk Counties, Long Island, New York

    USGS Publications Warehouse

    Eckhardt, D.A.; Flipse, W.J., Jr.; Oaksford, E.T.

    1989-01-01

    The chemical quality of groundwater in the upper glacial (water-table) aquifer beneath the 10 types of land-use areas of Nassau and Suffolk Counties, NY was examined to evaluate the effect of human activities on groundwater. The highest median chloride and total dissolved-solids concentrations were found in wells in high-density residential areas (more than five dwellings/acre), and the highest median nitrate, sulfate, and calcium concentrations were found in wells in agricultural and high density residential areas. Relatively low median concentrations of inorganic chemical constituents were found in wells in undeveloped and low-density residential areas (1 or fewer/acre): volatile organic compounds were rarely detected in these same areas. The highest concentrations and most frequent detection of volatile organic compounds were in industrial and commercial areas. The most commonly detected volatile organic compounds were 1,1,1-trichloroethane (24% of wells), tetrachloroethylene (20%), trichloroethylene (18%), chloroform (9%), and 1,2-dichloroethylene (5%). The spatial distributions of trichloroethylene, chloroform and other volatile organic compounds in the upper glacial aquifer are directly correlated with population density in the two-county area. (USGS)

  4. Response threshold levels of selected organic compounds for rainbow trout (Oncorhynchus mykiss)

    SciTech Connect

    Kaiser, K.L.E.; McKinnon, M.B.; Stendahl, D.H.; Pett, W.B.

    1995-12-01

    The responses of 27 organic compounds, mainly chloromethanes, -ethanes, -ethenes, and -phenols, were investigated by exposing rainbow trout fingerlings to low microgram-per-liter concentrations in a darkened flow-through system for up to 1 h. Responses by the fish were followed continuously by observing ventilation rates (frequency and amplitude), swimming patterns, and general activity using the low-voltage electric fields generated by the fishes` activity. The lowest level of response was found for trichloroethylene at 5 {micro}g/L. Dichloromethane, 1,1- and 1,2-dichloroethane, 1,1,1- and 1,1,2-trichloroethane, cis-1,2-dichloroethylene, 1,3-dichloropropene, and allyl acetate were responded to at concentrations of 10 {micro}g/L, carbon tetrachloride at 15 {micro}g/L, and 4-chlorophenol and 2,4-dichlorophenol at levels of 30 {micro}g/L. Unsubstituted phenol was not responded to at levels of up to 50 {micro}g/L.

  5. Surface acoustic wave sensors/gas chromatography; and Low quality natural gas sulfur removal and recovery CNG Claus sulfur recovery process

    SciTech Connect

    Klint, B.W.; Dale, P.R.; Stephenson, C.

    1997-12-01

    This topical report consists of the two titled projects. Surface Acoustic Wave/Gas Chromatography (SAW/GC) provides a cost-effective system for collecting real-time field screening data for characterization of vapor streams contaminated with volatile organic compounds (VOCs). The Model 4100 can be used in a field screening mode to produce chromatograms in 10 seconds. This capability will allow a project manager to make immediate decisions and to avoid the long delays and high costs associated with analysis by off-site analytical laboratories. The Model 4100 is currently under evaluation by the California Environmental Protection Agency Technology Certification Program. Initial certification focuses upon the following organics: cis-dichloroethylene, chloroform, carbon tetrachloride, trichlorethylene, tetrachloroethylene, tetrachloroethane, benzene, ethylbenzene, toluene, and o-xylene. In the second study the CNG Claus process is being evaluated for conversion and recovery of elemental sulfur from hydrogen sulfide, especially found in low quality natural gas. This report describes the design, construction and operation of a pilot scale plant built to demonstrate the technical feasibility of the integrated CNG Claus process.

  6. Treatability of TCE-contaminated clay soils at the Rinsewater Impoundment, Michoud Assembly Facility

    SciTech Connect

    Lucero, A.J.; Gilbert, V.P.; Hewitt, J.D.; Koran, L.J. Jr.; Jennings, H.L.; Donaldson, T.L.; West, O.R.; Cline, S.R.; Marshall, D.S.

    1995-02-01

    The Oak Ridge National Laboratory has conducted treatability studies on clay soils taken from the Rinsewater Impoundment at the National Aeronautics and Space Administration Michoud Assembly Facility. The soils are contaminated with up to 3000 mg/kg of trichloroethylene and cis-1,2-dichloroethylene, less than 10 mg/kg of trans-1,2-DCE, and less than 10 mg/kg of vinyl chloride. The goal of the study described in this report was to identify and test in situ technologies and/or develop a modified treatment regime to remove or destroy volatile organic compounds from the contaminated clay soils. Much of the work was based upon previous experience with mixed-region vapor stepping and mixed-region peroxidation. Laboratory treatments were performed on intact soil cores that were taken from contaminated areas at the Rinsewater Impoundment at MAF. Treatability studies were conducted on soil that was close to in situ conditions in terms of soil structure and contaminant concentrations.

  7. Development of an eco-sensor for the continuous monitoring of environmental volatile organic chlorinated compounds

    NASA Astrophysics Data System (ADS)

    Ishimori, Yoshio; Kawano, Koichiro; Shinozaki, Tsutomu; Mouri, Mitsuo; Kase, Takao; Tamiya, Eiichi; Ishizuka, Masaru

    2002-11-01

    In recent years, we have developed an advanced environmental monitoring system (AEMS) containing an eco-sensor, meaning a sensor for the measurement of environmental pollutants, based on lipid membranes, for continuous monitoring of underground water in industrial areas such as semiconductor factories (Ishimori Y, Tamura H, Kawano K, Aoyama N and Tamiya E 2000 Proc. Photonic East 2000 pp 43-50). The AEMS project is made up of three components as follows: (1) the eco-sensor, (2) prediction of plume propagation using a computer simulation technique, and (3) the environmental protection method. In this paper, we would like to focus on the study of the eco-sensor. We considered modified lipid membranes to serve as good models for cell membranes because they would be ideal hosts for receptor molecules of biological origin or disruptive environmental pollutants. Thus, we selected the lipid membrane as an environmental sensing element. In attempting to improve the applicability and the responsivity of bilayer lipid membranes (BLMs) in the eco-sensor, we have investigated automatic BLM preparation devices. An automatic BLM preparation device was made by use of an inkjet mechanism. The reproducibility of the BLM preparation was remarkably improved. The sensitivity to volatile organic chlorinated compounds such as cis-1, 2-dichloroethylene was of the order of 10 ppb using mono-olein BLMs even in real underground water. We have also been developing a smaller eco-sensor for practical use.

  8. Controlling the reactivity of chlorinated ethylenes with flavin mononucleotide hydroquinone.

    PubMed

    Ciptadjaya, Christopher G E; Guo, Wen; Angeli, Jayni M; Obare, Sherine O

    2009-03-01

    Reduction rate constants of the chlorinated ethylenes cis-1,2-dichloroethylene (cis-DCE), trichloroethylene (TCE), and tetrachloroethylene (PCE) reacted with flavin mononucleotide hydroquinone (FMNH2) under anoxic conditions were investigated. FMNH2 was produced in methanol solvent by the photoreduction of FMN. In aqueous solution, FMN was not fully reduced to FMNH2 but instead yielded the semiquinone radical FMNH*. However, when FMN was anchored to nanocrystalline TiO2, band gap irradiation resulted in electron transfer from the TiO2 conduction band to FMN, thus yielding FMNH2. The FMNH2 generated in aqueous solution on the TiO2 surface was a stronger reductant toward chlorinated ethylenes, relative to FMNH2 in solution. Furthermore, by combining the reactivity of the TiO2 conduction band electrons [TiO2(e-(CB)] with FMNH2, reduction rate constants for the chlorinated ethylenes increased by 2 orders of magnitude relative to FMNH2 alone. The results show how biological molecules such as FMNH2 could have significant effects toward the remediation of organic pollutants. PMID:19350940

  9. Effect of androgens and glucocorticoids on microbial growth and antimicrobial susceptibility.

    PubMed

    Plotkin, Balbina J; Roose, Robert J; Erikson, Quenby; Viselli, Susan M

    2003-12-01

    The effects of androgens, testosterone and dihydrotestosterone (DHT), of an environmental anti-androgen, 2,2-bis(4-chlorophenyl)-1,1-dichloroethylene (DDE), and of glucocorticoids, hydrocortisone and dexamethasone, on growth kinetics and antibiotic susceptibility of E. faecalis, E. coli, P. aeurginosa, and S. aureus were measured. For P. aeurginosa, the presence of either DHT or DDE caused at least a fourfold shift in the minimum inhibitory concentration (MIC) of cefepime and tobramycin. DHT and DDE also affected the response of E. faecalis to meropenem and norfloxacin, resulting in a shift from sensitive to intermediate resistance (four-fold increase in MIC). Hydrocortisone (2 microM) induced an increase in the sensitivity of S. aureus to erythromycin, as compared to hormone-free control (from 0.5 to 0.06 microg/mL). The susceptibility pattern of E. coli was unaffected by the hormones tested. These changes in susceptibility to antibiotics were unrelated to alterations in growth kinetics. For all organisms tested, the alterations in MICs occurred only in the presence of hormone, indicative of changes in the phenotype of these stable quality control strains. PMID:14756537

  10. Environmental contaminants in bald eagles in the Columbia River estuary

    SciTech Connect

    Anthony, R.G.; Garrett, M.G. ); Schuler, C.A. )

    1993-01-01

    Eggs, blood, and carcasses of bald eagles (Haliaeetus leucocephalus) and fish were collected and breeding success of eagles was monitored in the Columbia River estuary, 1980-87, to determine if contaminants were having an effect on productivity. High levels of dichloro diphenyl dichloroethylene (DDE), polychlorinated biphenyls (PCB's), and 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD) were found in eggs, blood from adults, and 2 eagle carcasses. Detectable levels of DDE and PCB's were found in blood of nestlings indicating they were exposed to these contaminants early in life. Increasing concentrations of DDE and PCB's with age also indicated accumulation of these contaminants. Adult eagles also had higher levels of mercury (Hg) in blood than subadults or young indicating accumulation with age. The high levels of DDE and PCB's were associated with eggshell thinning ([bar x] = 10%) and with productivity ([bar x] = 0.56 young/occupied site) that was lower than that of healthy populations (i.e., [ge]1.00 young/occupied site). DDE and PCB's had a deleterious effect on reproduction of bald eagles in the estuary. The role dioxins play in eagle reproduction remains unclear, but concentrations in eagle eggs were similar to those in laboratory studies on other species where dioxins adversely affected hatchability of eggs. Probable source of these contaminants include dredged river sediments and hydroelectric dams, and the proper management of each may reduce the amount of contaminants released into the Columbia River estuary. 46 refs., 1 fig., 4 tabs.

  11. Modelling of sequential groundwater treatment with zero valent iron and granular activated carbon.

    PubMed

    Bayer, Peter; Finkel, Michael

    2005-06-01

    Multiple contaminant mixtures in groundwater may not efficiently be treated by a single technology if contaminants possess rather different properties with respect to sorptivity, solubility, and degradation potential. An obvious choice is to use sequenced units of the generally accepted treatment materials zero valent iron (ZVI) and granular activated carbon (GAC). However, as the results of this modelling study suggest, the required dimensions of both reactor units may strongly differ from those expected on the grounds of a contaminant-specific design. This is revealed by performing an analysis for a broad spectrum of design alternatives through numerical experiments for selected patterns of contaminant mixtures consisting of monochlorobenzene, tetrachloroethylene, trichloroethylene (TCE), cis-1,2-dichloroethylene (cis-DCE), and vinyl chloride (VC). It is shown that efficient treatment can be achieved only if competitive sorption effects in the GAC unit as well as the formation of intermediate products in the ZVI unit are carefully taken into account. Cost-optimal designs turned out to vary extremely depending on the prevailing conditions concerning contaminant concentrations, branching ratios, and unit costs of both reactor materials. Where VC is the critical contaminant, due to high initial concentration or extensive production as an intermediate, two options are cost-effective: an oversized ZVI unit with an oversized GAC unit or a pure GAC reactor. PMID:15949610

  12. Kinetics of chlorinated ethylene dehalogenation under methanogenic conditions

    SciTech Connect

    Skeen, R.S.; Gao, J.; Hooker, B.S.

    1995-12-20

    Kinetics were determined for methanogenic activity and chlorinated ethylene dehalogenation by a methanol-enriched, anaerobic sediment consortium. The culture reductively dechlorinated perchloroethylene (PCE) to trichloroethylene (TCE), 1,1-dichloroethylene (1,1-DCE), vinylchloride (VC), and ethylene and ethane. The absence of methanol or the addition of 2-bromoethanesulfonic acid in the presence of methanol suppressed both methanogenic activity and dechlorination. In contrast, acetate production continued in the presence of 2-bromoethanesulfonic acid. These results suggest that dechlorination was strongly linked to methane formation and not to acetate production. A kinetic model, developed to describe both methanogenesis and dechlorination, successfully predicted experimentally measured concentrations of biomass, methane, substrate, and chlorinated ethylenes. The average maximum specific dehalogenation rates for PCE, TCE, 1,1-DCE, and VC were 0.9 {+-} 0.6, 0.4 {+-} 0.1, 12 {+-} 0.1, and 2.5 {+-} 1.7 {micro}mol contaminant/g {center_dot} DW/day, respectively. This pattern for dechlorination rates is distinctly different than that reported for transition metal cofactors, where rates drop by approximately one order of magnitude as each successive chlorine is removed. The experimental results and kinetic analysis suggest that it will be impractical to targeting methanol consuming methanogenic organisms for in-situ groundwater restoration.

  13. Kinetics of tetrachloroethylene-reductive dechlorination catalyzed by vitamin B{sub 12}

    SciTech Connect

    Burris, D.R.; Deng, B.; Buck, L.E.; Hatfield, K.

    1998-09-01

    Reductive dechlorination kinetics of tetrachloroethylene (PCE) to ethylene catalyzed by vitamin B{sub 12} using Ti[III] citrate as the bulk reductant was examined in a vapor-water batch system. A kinetic model incorporating substrate-B{sub 12} electron-transfer complex formation and subsequent product release was developed. The model also accounted for the primary reductive dechlorination pathways (hydrogenolysis and reductive {beta} elimination) and vapor/water-phase partitioning. Reaction rate constants were sequentially determined by fitting the model to experimental kinetic data while moving upward through consecutive reaction pathways. The release of product from the complex was found to be second order with respect to substrate concentration for both PCE and acetylene; all other substrates appeared to release by first order. Reductive {beta} elimination was found to be a significant reaction pathway for trichloroethylene (TCE), and chloroacetylene was observed as a reactive intermediate. Acetylene production appears to be primarily due to the reduction of chloroacetylene derived from TCE. The reduction of cis-dichloroethylene (cis-DCE), the primary DCE isomer formed, was extremely slow, leading to a significant buildup of cis-DCE. The kinetics of acetylene and vinyl chloride reduction appeared to be limited by the formation of relatively stable substrate-B{sub 12} complexes. The relatively simple model examined appears to adequately represent the main features of the experimental data.

  14. Health assessment for Whitmoyer Laboratories, Jackson Township, Lebanon County, Pennsylvania, Region 3. CERCLIS No. PAD003005014. Preliminary report

    SciTech Connect

    Not Available

    1988-11-17

    The Whitmoyer Laboratories 17.5-acre site is formerly an animal arsenical pharmaceutical manufacturing facility that operated from 1934 to 1984. In the early 1960s, approximately four million pounds of soluble arsenic wastes were placed into unlined lagoons. The environmental contamination on-site consists of arsenic and aniline in solid material in the concrete vault; arsenic, anile, 1,1-trichloroethane, and trans-1,2-dichloroethene in groundwater; arsenic in soil; and arsenic in surface water. Contamination off-site consists of arsenic, aniline, 1,1,1-trichloroethane in groundwater from an industrial well; arsenic in surface water; and arsenic in sediment. In addition, extensive sampling of domestic and industrial wells off-site has found arsenic, aniline, 1,2-dichloroethane, trans-1,2-dichloroethylene, trichloroethylene, 1,1,1-trichloroethane, and tetrachloroethylene. The site is considered to be of potential public health concern because of the risk to human health caused by the possibility of exposure to hazardous substances via contaminated groundwater, surface water, sediment, soil, and possibly air.

  15. Sonochemical degradation of perchloroethylene: the influence of ultrasonic variables, and the identification of products.

    PubMed

    Sáez, V; Esclapez, M D; Bonete, P; Walton, D J; Rehorek, A; Louisnard, O; González-García, J

    2011-01-01

    Sonochemistry is a technique that offers promise for pollutant degradation, but earlier studies on various chlorinated substrates do not give a definitive view of the effectiveness of this methodology. We now report a thorough study of ultrasonic operational variables upon perchloroethylene (PCE) degradation in water (variables include ultrasonic frequency, power and system geometry as well as substrate concentration) and we attempt to close the mass balance where feasible. We obtained fractional conversions of >97% showing very effective loss of pollutant starting material, and give mechanistic proposals for the reaction pathway based on cavitational phenomena inducing pyrolytic and free radical processes. We note major products of Cl(-) and CO(2)/CO, and also trichloroethylene (TCE) and dichloroethylene (DCE) at ppm concentrations as reported earlier. The formation at very low (ppb) concentration of small halocompounds (CHCl(3), CCl(4)) and also of higher-mass species, such as pentachloropropene, hexachloroethane, is noteworthy. But of particular importance in our work is the discovery of significant quantities of chloroacetate derivatives at ppm concentrations. Although these compounds have been described as by-products with other techniques such as radiolysis or photochemistry, this is the first time that these products have been identified in the sonochemical treatment of PCE; this allows a much more effective account of the mass balance and may explain earlier inconsistencies. This reaction system is now better identified, but a corollary is that, because these haloacetates are themselves species of some toxicity, the use of ultrasound here may not sufficiently diminish wastewater toxicity. PMID:20403718

  16. Degradation of 1,1,2,2-tetrachloroethane in a freshwater tidal wetland: Field and laboratory evidence

    SciTech Connect

    Lorah, M.M.; Olsen, L.D.

    1999-01-15

    Degradation reactions controlling the fate of 1,1,2,2-tetrachloroethane (PCA) in a freshwater tidal wetland that is a discharge area for a contaminated aquifer were investigated by a combined field and laboratory study. Samples from nested piezometers and porous-membrane sampling devices (peepers) showed that PCA concentrations decreased and that less chlorinated daughter products formed as the groundwater became increasingly reducing along upward flow paths through the wetland sediments. The is and trans isomers of 1,2-dichloroethylene (12DCE) and vinyl chloride (VC) were the predominant daughter products detected from degradation of PCA in the field and in microcosms constructed under methanogenic conditions. Significantly lower ratios of cis-12DCE to trans-12DCE were produced by PCA degradation than by degradation of trichloroethylene, a common co-contaminant with PCA. 1,1,2-Trichloroethane (112TCA) and 1,2-dichloroethane (12DCA) occurred simultaneously with 12DCE, indicating simultaneous hydrogenolysis and dichloroelimination of PCA. From an initial PCA concentration of about 1.5 {micro}mol/L, concentrations of PCA and its daughter products decreased to below detection within a 1.0-m vertical distance in the wetland sediments and within 34 days in the microcosms. The results indicate that natural attenuation of PCA through complete anaerobic biodegradation can occur in wetlands before sensitive surface water receptors are reached.

  17. Natural attenuation of chlorinated volatile organic compounds in a freshwater tidal wetland: Field evidence of anaerobic biodegradation

    USGS Publications Warehouse

    Lorah, M.M.; Olsen, L.D.

    1999-01-01

    Field evidence collected along two groundwater flow paths shows that anaerobic biodegradation naturally attenuates a plume of chlorinated volatile organic compounds as it discharges from an aerobic sand aquifer through wetland sediments. A decrease in concentrations of two parent contaminants, trichloroethylene (TCE) and 1,1,2,2-tetrachloroethane (PCA), and a concomitant increase in concentrations of anaerobic daughter products occurs along upward flow paths through the Wetland sediments. The daughter products 1,2-dichloroethylene, vinyl chloride, 1,1,2-trichloroethane, and 1,2-dichloroethane are produced from hydrogenolysis of TCE and from PCA degradation through hydrogenolysis and dichloroelimination (reductive dechlorination) pathways. Total concentrations of TCE, PCA, and their degradation products, however, decrease to below detection levels within 0.15-0.30 m of land surface. The enhanced reductive dechlorination of TCE and PCA in the wetland sediments is associated with the naturally higher concentrations of dissolved organic carbon and the lower redox state of the groundwater compared to the aquifer. This field study indicates that wetlands and similar organic-rich environments at groundwater/surface-water interfaces may be important in intercepting groundwater contaminated with chlorinated organics and in naturally reducing concentrations and toxicity before sensitive surface-water receptors are reached.

  18. Degradation of 1,1,2,2-tetrachloroethane in a freshwater tidal wetland: Field and laboratory evidence

    USGS Publications Warehouse

    Lorah, M.M.; Olsen, L.D.

    1999-01-01

    Degradation reactions controlling the fate of 1,1,2,2-tetrachloroethane (PCA) in a freshwater tidal wetland that is a discharge area for a contaminated aquifer were investigated by a combined field and laboratory study. Samples from nested piezometers and porous-membrane sampling devices (peepers) showed that PCA concentrations decreased and that less chlorinated daughter products formed as the groundwater became increasingly reducing along upward flow paths through the wetland sediments. The cis and trans isomers of 1,2-dichloroethylene (12DCE) and vinyl chloride (VC) were the predominant daughter products detected from degradation of PCA in the field and in microcosms constructed under methanogenic conditions. Significantly lower ratios of cis-12DCE to trans-12DCE were produced by PCA degradation than by degradation of trichloroethylene, a common co-contaminant with PCA. 1,1,2-Trichloroethane (112TCA) and 1,2-dichloroethane (12DCA) occurred simultaneously with 12DCE, indicating simultaneous hydrogenolysis and dichloroelimination of PCA. From an initial PCA concentration of about 1.5 ??mol/L, concentrations of PCA and its daughter products decreased to below detection within a 1.0-m vertical distance in the wetland sediments and within 34 days in the microcosms. The results indicate that natural attenuation of PCA through complete anaerobic biodegradation can occur in wetlands before sensitive surface water receptors are reached.

  19. Natural attenuation of chlorinated hydrocarbons in a freshwater wetland

    USGS Publications Warehouse

    Lora, Michelle M.; Olsen, Lisa D.; Smith, Barrett L.

    1997-01-01

    Natural attenuation of chlorinated volatile organic compounds (VOC's) occurs as ground water discharges from a sand aquifer to a freshwater wetland at Aberdeen Proving Ground, Md. Field and laboratory results indicate that biotransformation in the anaerobic wetland sediments is an important attenuation process. Relatively high concentrations of the parent compounds trichloroethylene (TCE) and 1,1,2,2-tetrachloroethane (PCA) and low or undetectable concentrations of daughter products were measured in the aquifer. In contrast, relatively high concentrations of the daughter products cis- and trans-1,2-dichloroethylene (12DCE); vinyl chloride (VC); 1,1,2-trichloroethane (112TCA); and 1,2-dichloroethane (12DCA) were measured in ground water in the wetland sediments, although total VOC concentrations decreased upward from about 1 mu mol/L (micromoles per liter) at the base of the wetland sediments to less than 0.2 near the surface. Microcosm experiments showed that 12DCE and VC are produced from anaerobic degradation of both TCE and PCA; PCA degradation also produced 112TCA and 12DCA.

  20. Biodegradation and biotransformation of groundwater pollutants, when present as mixtures, by soil microorganisms

    SciTech Connect

    Burback, B.L.

    1994-01-01

    The ability of soil microorganisms to metabolize mixtures of groundwater pollutants in pure culture and defined mixed culture was investigated. Mycobacterium vaccae strain JOB-5 catabolized acetone, cyclohexane, styrene, benzene, ethylbenzene, propylbenzene, dioxane and 1,2 dichloroethylene. Analysis indicated that the products of benzene degradation by M. vaccae were phenol and hydroquinone. The products of chlorobenzene, ethylbenzene, and propylbenzene degradation were identified as 4-chlorophenol, 4-ethylphenol, and 4-propylphenol. When toluene and benzene were present concomitantly toluene was degraded first. The presence of toluene promoted the degradation of styrene. These results suggested that components in mixtures may have a positive or a negative effect on the rates of biodegradation of other pollutants. The toxicity of seven major groundwater pollutants (benzene, chlorobenzene, propylbenzene, ethylbenzene, trichloroethylene, toluene, and styrene) and their metabolites to a soil mycobacterium (Mycobacterium vaccae strain JOB-5) that catabolized these pollutants was determined. Three metabolites were less toxic to M. vaccae than their parent compound. Three of the pollutants were less toxic than their metabolites. The metabolites 4-chlorophenol, 4-ethylphenol, and 4-propylphenol all inhibited the degradation of toluene by M. vaccae. A culture containing Mycobacterium vaccae and Rhodococcus sp. (strain R-22) was investigated to determine the effect two organisms would have on the catabolism of groundwater pollutants. The mixture mineralized benzene to CO[sub 2] at five times the amount of pure cultures. The physiological mechanism is described. This study demonstrates the complex interactions involved in the biodegradation of mixed groundwater pollutants.

  1. Biodegradation and biotransformation of groundwater pollutant mixtures by Mycobacterium vaccae.

    PubMed

    Burback, B L; Perry, J J

    1993-04-01

    Mycobacterium vaccae can catabolize a number of major groundwater pollutants. When added singly, acetone, cyclohexane, styrene, benzene, ethylbenzene, propylbenzene, dioxane, and 1,2-dichloroethylene can be catabolized by M. vaccae. Catabolism of a number of these chemicals was monitored by gas-chromatographic analysis. Gas-chromatographic analysis indicated that the products of benzene degradation are phenol and hydroquinone. The products of chlorobenzene and ethylbenzene degradation are 4-chlorophenol and 4-ethylphenol. The extent that some compounds were catabolized when present as mixtures was also investigated. When toluene and benzene were present concomitantly, toluene was catabolized and benzene oxidation was delayed. Although toluene promoted the degradation of styrene, a lower rate of toluene degradation occurred when styrene was present. Both 4-chlorophenol and 4-ethylphenol had an antagonistic effect on the ability of M. vaccae to degrade other aromatic compounds. Studies with [14C]benzene indicated that M. vaccae can mineralize small amounts of this compound. These results suggest that components in mixtures may have a positive or a negative effect on the rates of biodegradation of other pollutants. PMID:8476280

  2. Degradation of trichloroethylene by toluene dioxygenase in whole-cell studies with Pseudomonas putida F1.

    PubMed Central

    Wackett, L P; Gibson, D T

    1988-01-01

    Toluene-induced cells of Pseudomonas putida F1 removed trichloroethylene from growth media at a significantly greater initial rate than the methanotroph Methylosinus trichosporium OB3b. With toluene-induced P. putida F1, the initial degradation rate varied linearly with trichloroethylene concentration over the range of 8 to 80 microM (1.05 to 10.5 ppm). At 80 microM (10.5 ppm) trichloroethylene and 30 degrees C, the initial rate was 1.8 nmol/min per mg of total cell protein, but the rate decreased rapidly with time. A series of mutant strains derived from P. putida F1 that are defective in the todC gene, which encodes the oxygenase component of toluene dioxygenase, failed to degrade trichloroethylene and to oxidize indole to indigo. A spontaneous revertant selected from a todC culture regained simultaneously the abilities to oxidize toluene, to form indigo, and to degrade trichloroethylene. The three isomeric dichloroethylenes were degraded by P. putida F1, but tetrachloroethylene, vinyl chloride, and ethylene were not removed from incubation mixtures. PMID:3415234

  3. Biodegradation and biotransformation of groundwater pollutant mixtures by Mycobacterium vaccae.

    PubMed Central

    Burback, B L; Perry, J J

    1993-01-01

    Mycobacterium vaccae can catabolize a number of major groundwater pollutants. When added singly, acetone, cyclohexane, styrene, benzene, ethylbenzene, propylbenzene, dioxane, and 1,2-dichloroethylene can be catabolized by M. vaccae. Catabolism of a number of these chemicals was monitored by gas-chromatographic analysis. Gas-chromatographic analysis indicated that the products of benzene degradation are phenol and hydroquinone. The products of chlorobenzene and ethylbenzene degradation are 4-chlorophenol and 4-ethylphenol. The extent that some compounds were catabolized when present as mixtures was also investigated. When toluene and benzene were present concomitantly, toluene was catabolized and benzene oxidation was delayed. Although toluene promoted the degradation of styrene, a lower rate of toluene degradation occurred when styrene was present. Both 4-chlorophenol and 4-ethylphenol had an antagonistic effect on the ability of M. vaccae to degrade other aromatic compounds. Studies with [14C]benzene indicated that M. vaccae can mineralize small amounts of this compound. These results suggest that components in mixtures may have a positive or a negative effect on the rates of biodegradation of other pollutants. PMID:8476280

  4. The kinetics of the combustion of trichloroethylene for low Cl/H ratios

    SciTech Connect

    Werner, J.H.; Cool, T.A.

    2000-01-01

    A kinetic model has been developed for the combustion of trichloroethylene (TCE) under low Cl/H ratio conditions. Flame species concentration profiles, measured for CH{sub 4}/O{sub 2}/Ar flames, reveal that the most important reaction channels in the decomposition of TCE in the CH{sub 4}/TCE/O{sub 2}/Ar flame are the displacement by H atoms of Cl atoms from TCE,1,1-dichloroethylene (DCE), and vinyl chloride. The displacement of Cl atoms from TCE by OH also contributes to the decomposition of TCE, and leads to the production of 2,2-dichloroethanol, a species unobserved in previous flame studies. Other species found in large concentrations in the present CH{sub 4}/TCE/O{sub 2}/Ar flames, but not observed in previous TCE/O{sub 2}/Ar flame studies at higher chlorine-too-hydrogen ratios, are ketene, chloroketene, and dichloroketene. Finally, the presence of TCE catalyzes the formation of C{sub 3}-C{sub 6} hydrocarbons. The presence of significant concentrations of C{sub 3}H{sub 3}, C{sub 3}H{sub 4}, and C{sub 6}H{sub 6} is consistent with odd carbon species mechanisms previously suggested for benzene formation in hydrocarbon flames.

  5. Cometabolic degradation of TCE and DCE without intermediate toxicity

    SciTech Connect

    Bielefeldt, A.R.; Stensel, H.D.; Strand, S.E.

    1995-11-01

    Trichloroethylene (TCE) and cis-1,2-dichloroethylene (DCE) cometabolic degradation by a filamentous, phenol-oxidizing enrichment from a surface-water source were investigated in batch tests. No intermediate toxicity effects were evident during TCE or DCE degradation for loadings up to 0.5 mg TCE/mg VSS or 0.26 mg DCE/mg VSS. Phenol addition up to 40 mg/L did not inhibit TCE or DCE degradation. TCE specific degradation rates ranged from 0.28 to 0.51 g TCE/g VSS-d with phenol present, versus an average endogenous rate of 0.18 g TCE/g VSS-d. DCE specific degradation rates ranged from 0.79 to 2.92 g DCE/g VSS-d with phenol present, versus 0.27 to 1.5 g DCE/g VSS-d for endogenous conditions. There was no inhibition of DCE degradation rates at concentrations as high as 83 mg/L. TCE degradation rates declined between 40 and 130 mg/L TCE. Perchloroethylene, 1,1,1-trichloroethane, and chloroform were not degraded.

  6. PBDEs and other POPs in urban birds of prey partly explained by trophic level and carbon source.

    PubMed

    Elliott, John E; Brogan, Jason; Lee, Sandi L; Drouillard, Ken G; Elliott, Kyle H

    2015-08-15

    As urban sprawl and agricultural intensification continue to invade prime wildlife habitat, some animals, even apex predators, are managing to adapt to this new environment. Chemical pollution is one of many stressors that wildlife encounter in urban environments. Predators are particularly sensitive to persistent chemical pollutants because they feed at a high trophic level where such pollution is biomagnified. To examine levels of pollution in urban birds of prey in the Lower Mainland region of British Columbia, Canada, we analyzed persistent organic contaminants in adult birds found dead of trauma injury. The hepatic geometric mean concentration of sum polybrominated diphenyl ethers (∑PBDEs) in 13 Cooper's hawks (Accipiter cooperii) from Greater Vancouver was 1873 ng/g (lipid weight) with one bird reaching 197,000n g/g lipid weight, the highest exposure reported to date for a wild bird. Concentrations of ∑PBDEs, ∑PCBs (polychlorinated biphenyls) and, surprisingly, cyclodiene insecticides were greatest in the urban environment while those of DDE (1,1-dichloroethylene bis[p-chlorophenyl) were highest in a region of intensive agriculture. The level of most chlorinated and brominated contaminants increased with trophic level (δ(15)N). The concentrations of some contaminants, PBDEs in particular, in these birds of prey may have some toxicological consequences. Apex predators in urban environments continue to be exposed to elevated concentrations of legacy pollutants as well as more recent brominated pollutants. PMID:25897724

  7. Microextraction of priority pollutants

    SciTech Connect

    Leepipatriboon, S.

    1984-01-01

    Some of the priority pollutants, e.g., aromatic hydrocarbons, halogenated aromatic hydrocarbons and halogenated alkanes and alkenes have been studied by a microextraction technique. The compounds studied were benzene, toluene, and ethylbenzene for aromatic hydrocarbons; chlorobenzene, m-dichlorobenzene, p-dichlorobenzene, and o-dichlorobenzene for halogenated aromatic hydrocarbons; and trans-1,2-dichloroethylene, 1,1-dichloroethane, 1,1,2,2-tetrachloroethane, choloroform, ethylene chloride, 1,1,1-trichloroethane, carbon tetrachloride, methylene chloride, bromodichloromethane, 1,2-dichloropropane, trichloroethylene and bromoform for halogenated alkanes and alkenes. The organic solvent-to-water sample ratios of study were 1:9, 5:5 and 8:2, respectively. Solvent extractability effect of carbon disulfide, methylene chloride and hexane or iso-octane and the effect of salts, e.g., saturated sodium chloride solution, saturated sodium sulfate solution, 2.00 g of sodium chloride and 2.00 g of sodium sulfate on the percent recovery were investigated in this study. This technique is based on the extraction into an organic solvent phase followed by the measurement of the peak area by a flame ionization detector. Gas chromatography and the internal standard technique were used throughout the stud. The gas chromatographic conditions for each system of study were reported. The standard deviation of this study ranged from 1-16%. The distribution constant, K{sub D}, and the results of percent recovery for each compound are discussed.

  8. Mixed Waste Management Facility groundwater monitoring report: Third quarter 1994

    SciTech Connect

    Not Available

    1994-12-01

    Currently, 125 wells monitor groundwater quality in the uppermost aquifer beneath the Mixed Waste Management Facility (MWMF) at the Savannah River Site. Samples from the wells are analyzed for selected heavy metals, herbicides/pesticides, indicator parameters, radionuclides, volatile organic compounds, and other constituents. As in previous quarters, tritium and trichloroethylene were the most widespread elevated constituents during third quarter 1994. Sixty-four (51%) of the 125 monitoring wells contained elevated tritium activities. Trichloroethylene concentrations exceeded the final PDWS in 22 (18%) wells. Chloroethene, 1,1-dichloroethylene, and tetrachloroethylene, elevated in one or more wells during third quarter 1994, also occurred in elevated levels during second quarter 1994. These constituents generally were elevated in the same wells during both quarters. Gross alpha, which was elevated in only one well during second quarter 1994, was elevated again during third quarter. Mercury, which was elevated during first quarter 1994, was elevated again in one well. Dichloromethane was elevated in two wells for the first time in several quarters.

  9. Combined removal of a BTEX, TCE, and cis-DCE mixture using Pseudomonas sp. immobilized on scrap tyres.

    PubMed

    Lu, Qihong; de Toledo, Renata Alves; Xie, Fei; Li, Junhui; Shim, Hojae

    2015-09-01

    The simultaneous aerobic removal of a mixture of benzene, toluene, ethylbenzene, and o,m,p-xylene (BTEX); cis-dichloroethylene (cis-DCE); and trichloroethylene (TCE) from the artificially contaminated water using an indigenous bacterial isolate identified as Pseudomonas plecoglossicida immobilized on waste scrap tyres was investigated. Suspended and immobilized conditions were compared for the removal of these volatile organic compounds. For the immobilized system, toluene, benzene, and ethylbenzene were completely removed, while the highest removal efficiencies of 99.0 ± 0.1, 96.8 ± 0.3, 73.6 ± 2.5, and 61.6 ± 0.9% were obtained for o-xylene, m,p-xylene, TCE, and cis-DCE, respectively. The sorption kinetics of contaminants towards tyre surface was also evaluated, and the sorption capacity generally followed the order of toluene > benzene > m,p-xylene > o-xylene > ethylbenzene > TCE > cis-DCE. Scrap tyres showed a good capability for the simultaneous sorption and bioremoval of BTEX/cis-DCE/TCE mixture, implying a promising waste material for the removal of contaminant mixture from industrial wastewater or contaminated groundwater. PMID:25956516

  10. Sanitary Landfill 1991 annual groundwater monitoring report

    SciTech Connect

    Thompson, C.Y.; Norrell, G.T.; Bennett, C.B.

    1992-02-01

    The Savannah River Site (SRS) Sanitary Landfill is an approximately seventy acre site located just south of SRS Road C between the Savannah River Site`s B-Area and Upper Three Runs Creek. Results from the first through third quarter 1991 groundwater monitoring date continue to show evidence of elevated levels of several hazardous constituents beneath the Sanitary Landfill: tritium, vinyl chloride, total radium, cadmium, 1,1,1-trichloroethane, 1,2 dichloroethane, 1,4 dichlorobenzene, trichloroethylene (TCE), tetrachloroethylene, and 1,1 dichloroethylene in excess of the primary drinking water standards were observed in at least one well monitoring the Sanitary Landfill during the third quarter of 1991. All of these constituents, except radium, were observed in the lower half of the original thirty-two acre site or the southern expansion site. Trichloroethylene and vinyl chloride are the primary organic contaminants in groundwater beneath the Sanitary Landfill. Vinyl chloride has become the primary contaminant during 1991. Elevated levels of benzene were consistently detected in LFW 7 in the past, but were not present in any LFW wells during the third quarter of 1991. A minor tritium plume is present in the central part of original thirty-two acre landfill. Elevated levels of tritium above the PDWS were consistently present in LFW 10A through 1991. This well has exhibited elevated tritium activities since the second quarter of 1989. Contaminant concentrations in the Sanitary Landfill are presented and discussed in this report.

  11. Sanitary Landfill 1991 annual groundwater monitoring report

    SciTech Connect

    Thompson, C.Y.; Norrell, G.T.; Bennett, C.B.

    1992-02-01

    The Savannah River Site (SRS) Sanitary Landfill is an approximately seventy acre site located just south of SRS Road C between the Savannah River Site's B-Area and Upper Three Runs Creek. Results from the first through third quarter 1991 groundwater monitoring date continue to show evidence of elevated levels of several hazardous constituents beneath the Sanitary Landfill: tritium, vinyl chloride, total radium, cadmium, 1,1,1-trichloroethane, 1,2 dichloroethane, 1,4 dichlorobenzene, trichloroethylene (TCE), tetrachloroethylene, and 1,1 dichloroethylene in excess of the primary drinking water standards were observed in at least one well monitoring the Sanitary Landfill during the third quarter of 1991. All of these constituents, except radium, were observed in the lower half of the original thirty-two acre site or the southern expansion site. Trichloroethylene and vinyl chloride are the primary organic contaminants in groundwater beneath the Sanitary Landfill. Vinyl chloride has become the primary contaminant during 1991. Elevated levels of benzene were consistently detected in LFW 7 in the past, but were not present in any LFW wells during the third quarter of 1991. A minor tritium plume is present in the central part of original thirty-two acre landfill. Elevated levels of tritium above the PDWS were consistently present in LFW 10A through 1991. This well has exhibited elevated tritium activities since the second quarter of 1989. Contaminant concentrations in the Sanitary Landfill are presented and discussed in this report.

  12. Polydimethylsiloxane-based permeation passive air sampler. Part I: Calibration constants and their relation to retention indices of the analytes.

    PubMed

    Seethapathy, Suresh; Górecki, Tadeusz

    2011-01-01

    A simple and cost effective permeation passive sampler equipped with a polydimethylsiloxane (PDMS) membrane was designed for the determination of time-weighted average (TWA) concentrations of volatile organic compounds (VOCs) in air. Permeation passive samplers have significant advantages over diffusive passive samplers, including insensitivity to moisture and high face velocities of air across the surface of the sampler. Calibration constants of the sampler towards 41 analytes belonging to alkane, aromatic hydrocarbon, chlorinated hydrocarbon, ester and alcohol groups were determined. The calibration constants allowed for the determination of the permeability of PDMS towards the selected analytes. They ranged from 0.026 cm² min⁻¹ for 1,1-dichloroethylene to 0.605 cm² min⁻¹ for n-octanol. Further, the mechanism of analyte transport across PDMS membranes allowed for the calibration constants of the sampler to be estimated from the linear temperature programmed retention indices (LTPRI) of the analytes, determined using GC columns coated with pure PDMS stationary phases. Statistical analysis using Student's t test indicated that there was no significant difference at the 95% probability level between the experimentally obtained calibration constants and those estimated using LTPRI for most analyte groups studied. This correlation allows the estimation of the calibration constants of compounds not known to be present at the time of sampler deployment, which makes it possible to determine parameters like total petroleum hydrocarbons in the vapor phase. PMID:21112594

  13. Biodegradation of trichloroethylene and biomanipulation of aquifers. Technical report (Final)

    SciTech Connect

    Jaffe, P.R.; Taylor, S.W.; Baek, N.H.; Christopher, P.; Milly, D.

    1988-08-01

    Three distinct aspects of the biodegradation process in a porous media were addressed. The effect of the trichloroethylene(TCE) concentration on bacterial activity was investigated. The results showed that the dissolved-phase concentration directly affects the bacterial activity. For aerobic soils, LD50 for water concentrations ranged between 200-300 mg/l for CO/sub 2/ evolution, and 80 to 150 mg/l for dehydrogenase activity. The degradation of TCE and its intermediates by mixed cultures containing fermenters and methanogens was investigated. Results showed that fermenters play an important role in this process and that the degradation rate correlates with the methanogenic activity. It was shown that TCE can be degraded by these mixed cultures via 1,1-dichloroethylene to vinyl chloride, to chloroethane which is readily degradable. Kinetic rates were obtained for this degradation process and normalized with respect to the methane production. The effect of biomass production in porous media on the permeability and dispersivity was investigated. Experimental results showed that the permeability of a sandy media depends on the biomass if the biomass is less than 0.4 mg of organic carbon/cu cm, and becomes independent of the biomass for higher values. Changes in permeability and dispersivity as a function of the biofilm thickness were modeled successfully using a modified cut-and-random-rejoin-type model.

  14. Degradation of TCE using sequential anaerobic biofilm and aerobic immobilized bed reactor

    NASA Technical Reports Server (NTRS)

    Chapatwala, Kirit D.; Babu, G. R. V.; Baresi, Larry; Trunzo, Richard M.

    1995-01-01

    Bacteria capable of degrading trichloroethylene (TCE) were isolated from contaminated wastewaters and soil sites. The aerobic cultures were identified as Pseudomonas aeruginosa (four species) and Pseudomonas fluorescens. The optimal conditions for the growth of aerobic cultures were determined. The minimal inhibitory concentration values of TCE for Pseudomonas sps. were also determined. The aerobic cells were immobilized in calcium alginate in the form of beads. Degradation of TCE by the anaerobic and dichloroethylene (DCE) by aerobic cultures was studied using dual reactors - anaerobic biofilm and aerobic immobilized bed reactor. The minimal mineral salt (MMS) medium saturated with TCE was pumped at the rate of 1 ml per hour into the anaerobic reactor. The MMS medium saturated with DCE and supplemented with xylenes and toluene (3 ppm each) was pumped at the rate of 1 ml per hour into the fluidized air-uplift-type reactor containing the immobilized aerobic cells. The concentrations of TCE and DCE and the metabolites formed during their degradation by the anaerobic and aerobic cultures were monitored by GC. The preliminary study suggests that the anaerobic and aerobic cultures of our isolates can degrade TCE and DCE.

  15. Developments toward a Low-Cost Approach for Long-Term, Unattended Vapor Intrusion Monitoring

    PubMed Central

    Tolley, William K.

    2014-01-01

    There are over 450,000 sites contaminated by chemicals in the US. This large number of contaminated sites and the speed of subsurface migration of chemicals pose considerable risk to nearby residences and commercial buildings. The high costs for monitoring around these site stem from the labor involved in placing and replacing the passive sorbent vapor samplers and the resultant laboratory analysis. This monitoring produces sparse data sets that do not track temporal changes well. To substantially reduce costs and better track exposures, less costly, unattended systems for monitoring soil gases and vapor intrusion into homes and businesses are desirable to aid in the remediation of contaminated sites. This paper describes progress toward the development of an inexpensive system specifically for monitoring vapor intrusion; the system can operate repeatedly without user intervention with low detection limits (1 × 10−9, or 1 part-per-billion). Targeted analytes include chlorinated hydrocarbons (dichloroethylene, trichloroethane, trichloroethylene, and perchloroethylene) and benzene. The system consists of a trap-and-purge preconcentrator for vapor collection in conjunction with a compact gas chromatography instrument to separate individual compounds. Chemical detection is accomplished with an array of chemicapacitors and a metal-oxide semiconductor combustibles sensor. Both the preconcentrator and the chromatography column are resistively heated. All components are compatible with ambient air, which serves as the carrier gas for the gas chromatography and detectors. PMID:24903107

  16. Health assessment for Thermo Chem, Inc. , Muskegon, Michigan, Region 5. CERCLIS No. MID044567162. Preliminary report

    SciTech Connect

    Not Available

    1988-11-28

    Thermo-Chem, Inc. is listed on the National Priorities List. The Thermo-Chem, Inc. site is located in Muskegon County, Michigan. Thermo-Chem, Inc. was involved in solvent reprocessing and liquid-waste disposal, beginning operations in 1969 and continuing until August 1980. The company received paint waste, antifreeze waste, and spent halogenated and nonhalogenated solvents. A soil-gas and soil-sampling survey detected: trichloroethene (TCE), 24,000 ppb; tetrachloroethene (PCE), 400,000 ppb; 1,1,1-trichloroethane, 16,000 ppb; 1,2-dichloroethylene, 4,500 ppb; toluene, 92,000 ppb; ethyl benzene, 450,000 ppb; and xylene, 2,100,000 ppb. The following contaminants and their respective concentrations in ppb were detected in the monitoring wells in 1986 as part of the hydrogeologic investigation: TCE, 67,000; PCE, 54,000; 1,1,1-trichloroethane, 26,000; 1,2-dichloroethene, 7,200; toluene, 100,000; ethyl benzene, 2,000; benzene, 5,000; methylene chloride, 1,800 and xylene, 17,000. No contamination has been detected in nearby residential wells. The site is of potential public health concern because of the risk to human health that could result from possible exposure to hazardous substances at levels that may result in adverse health effects over time. Human exposure to several organic contaminants may occur via contact with soil, surface water, or ground water contamination.

  17. Sorption studies of VOCs (volatile organic compounds) related to soil/ground water contamination at LLNL (Lawrence Livermore National Laboratory)

    SciTech Connect

    Bishop, D.J.; Knezovich, J.P.; Rice, D.W. Jr.

    1989-08-01

    In 1980, Lawrence Livermore National Laboratory (LLNL) initiated a preliminary ground water study beneath and in the vicinity of the LLNL site in Livermore, California. Findings from that study indicated that volatile organic compounds (VOCs), primarily tetrachloroethylene (PCE) and trichloroethylene (TCE), were present in local ground water. Subsequent sampling results showed several locations with VOCs in the parts-per-billion range, and three areas where parts-per-million concentrations were detected. Subsequently, more than 200 wells were drilled and tested during investigations to assess the lateral and stratigraphic extent of ground water contamination and to understand the hydrogeologic characteristics under the Laboratory and adjacent affected areas. Although PCE and TCE predominate, dichloroethanes, dichloroethylenes, and carbon tetrachloride have been detected in ground water at concentrations exceeding California Department of Health Services recommended action levels. In order to predict the rate and extent of movement of the VOCs in ground water, it is essential to understand the sorptive properties of these compounds in relation to the subsurface soils that exist in this area. TCE and PCE were selected for study initially because of their predominance in the contaminant plume. Additional tests were performed using 1,2-dichloroethane (DCA), 1,2-dichloroethene (DCE), and chloroform (CF). 28 refs., 4 figs., 7 tabs.

  18. Evaluating chlorine isotope effects from isotope ratios and mass spectra of polychlorinated molecules.

    PubMed

    Elsner, Martin; Hunkeler, Daniel

    2008-06-15

    Compound-specific chlorine isotope analysis receives much interest to assess the fate of chlorinated hydrocarbons in contaminated environments. This paper provides a theoretical basis to calculate isotope ratios and quantify isotope fractionation from ion-current ratios of molecular- and fragment-ion multiplets. Because both (35)Cl and (37)Cl are of high abundance, polychlorinated hydrocarbons consist of molecules containing different numbers of (37)Cl denoted as isotopologues. We show that, during reactions, the changes in isotopologue ratios are proportional to changes in the isotope ratio assuming a nonselective isotope distribution in the initial compound. This proportionality extents even to fragments formed in the ion source of a mass spectrometer such as C 2Cl 2 (double dechlorinated fragment of perchloroethylene, PCE). Fractionation factors and kinetic isotope effects (KIE) may, therefore, be evaluated from isotope, isotopologue or even fragment ratios according to conventional simple equations. The proportionality is exact with symmetric molecules such as dichloroethylene (DCE) and PCE, whereas it is approximately true with molecules containing nonreactive positions such as trichloroethylene (TCE). If in the latter case isotope ratios are derived from dechlorinated fragments, e.g., C 2HCl 2, it is important that fragmentation in the ion source affect all molecular positions alike, as otherwise isotopic changes in reactive positions may be underrepresented. PMID:18484745

  19. Health assessment for Lacks Industries, Inc. , Grand Rapids, Kent County, Michigan, Region 5. CERCLIS No. MID006014666. Preliminary report

    SciTech Connect

    Not Available

    1989-04-10

    The Lacks Industries, Inc. site, in Grand Rapids, Michigan, has been delisted from the National Priorities List and is being regulated under the Resource Conservation and Recovery Act. Lacks Industries, Inc. discontinued electroplating operations and die casting for the automobile industry in July 1984 at the plant site. The plant is now used for painting and assembling of plastic parts for automobiles. Previously, plating wastes were discharged to two seepage ponds. It is reported that the prior owner (pre-1960) dumped trichloroethylene (TCE) and tetrachloroethylene (PCE) and metal solutions into a pit in the ground above which was built part of the Lacks Industries building. TCE and PCE were identified in all four downgradient monitoring wells with maximum concentrations of 17 parts per billion (ppb) and 89 ppb, respectively. Toluene (8 ppb), m-xylene (2 ppb) and cis-1,2-dichloroethylene (240 ppb) were each identified in one downgradient well. The two upgradient wells, which are supposed to represent background concentrations, had PCE concentrations of 67 ppb and 74 ppb. Several homes in the area had elevated concentrations of volatile organic compounds (VOCs), nickel, and total chromium. The site is of potential public health concern because of the risk to human health that could result from possible exposure to hazardous substances at levels that may result in adverse health effects over time.

  20. Health assessment for Long Prairie ground water contamination site, Long Prairie, Minnesota, Region 5. CERCLIS No. MND980904072. Final report

    SciTech Connect

    Not Available

    1989-06-27

    The ground-water contamination in Long Prairie, Minnesota is listed on the National Priorities List. At the site, two municipal wells and many private wells are contaminated with tetrachloroethylene (PCE) and its degradative by-products trichloroethylene (TCE), cis-1,2-dichloroethylene (DCE) and vinyl chloride. The source of the contamination is a dry-cleaning establishment located in the center of town. Maximum contaminant concentrations found in ground water in the municipal wells are 280 micro g/l PCE, 11 micro g/l TCE and micro g/l DCE. The maximum concentrations found in the private well are 1000 micro g/l PCE, 110 micro g/l TCE and 250 micro g/l DCE. Monitoring wells contain as much as 22,000 micro g/l PCE, 45 micro g/l TCE and 40 micro g/l DCE. The site is considered to be of public health concern because of the risk to human health caused by the likelihood of exposure to hazardous substances.

  1. Integrated Geophysical Investigation of Preferential Flow Paths at the Former Tyson Valley Powder Farm near Eureka, Missouri, May 2006

    USGS Publications Warehouse

    Burton, Bethany L.; Ball, Lyndsay B.; Stanton, Gregory P.; Hobza, Christopher M.

    2009-01-01

    In May 2006, the U.S. Geological Survey, in cooperation with the U.S. Army Corps of Engineers, conducted surface and borehole geophysical surveys at the former Tyson Valley Powder Farm near Eureka, Mo., to identify preferential pathways for potential contaminant transport along the bedrock surface and into dissolution-enhanced fractures. The Tyson Valley Powder Farm was formerly used as a munitions storage and disposal facility in the 1940s and 1950s, and the site at which the surveys were performed was a disposal area for munitions and waste solvents such as trichloroethylene and dichloroethylene. Direct-current resistivity and seismic refraction data were acquired on the surface; gamma, electromagnetic induction, and full waveform sonic logs were acquired in accessible boreholes. Through the combined interpretation of the seismic refraction tomographic and resistivity inversion results and borehole logs, inconsistencies in the bedrock surface were identified that may provide horizontal preferential flow paths for dense nonaqueous phase liquid contaminants. These results, interpreted and displayed in georeferenced three-dimensional space, should help to establish more effective monitoring and remediation strategies.

  2. Electron donor preference of a reductive dechlorinating consortium

    USGS Publications Warehouse

    Lorah, M.M.; Majcher, E.; Jones, E.; Driedger, G.; Dworatzek, S.; Graves, D.

    2005-01-01

    A wetland sediment-derived microbial consortium was developed by the USGS and propagated in vitro to large quantities by SiREM Laboratory for use in bioaugmentation applications. The consortium had the capacity to completely dechlorinate 1,1,2,2-tetrachloroethene, tetrachloroethylene, trichloroethylene, 1,1,2-trichloroethane, cis- and trans-1,2-dichoroethylene, 1.1-dichloroethylene, 1,2-dichloroethane, vinyl chloride, carbon tetrachloride and chloroform. A suite of electron donors with characteristics useful for bioaugmentation applications was tested. The electron donors included lactate (the donor used during WBC-2 development), ethanol, chitin (Chitorem???), hydrogen releasing compound (HRC???), emulsified vegetable oil (Newman Zone???), and hydrogen gas. Ethanol, lactate, and chitin were particularly effective with respect to stimulating, supporting, and sustaining reductive dechlorination of the broad suite of chemicals that WBC-2 biodegraded. Chitorem??? was the most effective "slow release" electron donor tested. This is an abstract of a paper presented at the Proceedings of the 8th International In Situ and On-Site Bioremediation Symposium (Baltimore, MD 6/6-9/2005).

  3. A mass balance study of the phytoremediation of perchloroethylene-contaminated groundwater

    PubMed Central

    James, C. Andrew; Xin, Gang; Doty, Sharon L.; Muiznieks, Indulis; Newman, Lee; Strand, Stuart E.

    2010-01-01

    A mass balance study was performed under controlled field conditions to investigate the phytoremediation of perchloroethylene (PCE) by hybrid poplar trees. Water containing 7–14 mg L−1 PCE was added to the test bed. Perchloroethylene, trichloroethylene, and cis-dichloroethylene were detected in the effluent at an average of 0.12 mg L−1, 3.9 mg L−1, and 1.9 mg L−1, respectively. The total mass of chlorinated ethenes in the water was reduced by 99%. Over 95% of the recovered chlorine was as free chloride in the soil, indicating near-complete dehalogenation of the PCE. Transpiration, volatilization, and accumulation in the trees were all found to be minor loss mechanisms. In contrast, 98% of PCE applied to an unplanted soil chamber was recovered as PCE in the effluent water or volatilized into the air. These results suggest that phytoremediation can be an effective method for treating PCE-contaminated groundwater in field applications. PMID:19345455

  4. Exposure of Cucurbita pepo to DDE-contamination alters the endophytic community: A cultivation dependent vs a cultivation independent approach.

    PubMed

    Eevers, N; Hawthorne, J R; White, J C; Vangronsveld, J; Weyens, N

    2016-02-01

    2,2-bis(p-chlorophenyl)-1,1-dichloro-ethylene (DDE) is the most abundant and persistent degradation product of the pesticide 2,2-bis(p-chlorophenyl)-1,1,1-trichloroethane (DDT) and is encountered in contaminated soils worldwide. Both DDE and DDT are classified as Persistent Organic Pollutants (POPs) due to their high hydrophobicity and potential for bioaccumulation and biomagnification in the food chain. Zucchini (Cucurbita pepo ssp. pepo) has been shown to accumulate high concentrations of DDE and other POPs and has been proposed as a phytoremediation tool for contaminated soils. The endophytic bacteria associated with this plant may play an important role in the remedial process. Therefore, this research focuses on changes in endophytic bacterial communities caused by the exposure of C. pepo to DDE. The total bacterial community was investigated using cultivation-independent 454 pyrosequencing, while the cultivable community was identified using cultivation-dependent isolation procedures. For both procedures, increasing numbers of endophytic bacteria, as well as higher diversities of genera were observed when plants were exposed to DDE. Several bacterial genera such as Stenotrophomonas sp. and Sphingomonas sp. showed higher abundance when DDE was present, while, for example Pseudomonas sp. showed a significantly lower abundance in the presence of DDE. These findings suggest tolerance of different bacterial strains to DDE, which might be incorporated in further investigations to optimize phytoremediation with the possible use of DDE-degrading endophytes. PMID:26683261

  5. Sport fish consumption and body burden levels of chlorinated hydrocarbons: a study of Wisconsin anglers

    SciTech Connect

    Fiore, B.J.; Anderson, H.A.; Hanrahan, L.P.; Olson, L.J.; Sonzogni, W.C.

    1989-03-01

    Sport-caught fish consumption is the major source of polychlorinated biphenyls (PCBs) exposure for the general population. To assess this and 2,2'-bis-(p-chlorophenyl)-1,1-dichloroethylene (DDE) exposure, we surveyed 801 Wisconsin anglers for fishing and consumption habits and comprehension of and compliance with the Wisconsin fish consumption health advisory. The mean annual number of sport-caught fish meals was 18. Seventy-two percent of anglers were familiar with the health advisory and 57% had changed their fishing or fish consumption habits as a result of the advisory. The mean PCB serum congener sum level for 192 anglers was 2.2 micrograms/l (range = nondetectable to 27.1 micrograms/l); mean DDE was 6.3 micrograms/l (range = nondetectable to 40.0 micrograms/l). Statistically significant positive Spearman correlations were observed between sport-caught fish meals and PCB and DDE sera levels (R = .21 and .14, respectively) and between kilograms of fish caught and PCB sera levels (R = .25). These results demonstrate that anglers may provide a population for assessment of PCBs and DDE associated morbidity and mortality.

  6. Chloroform Cometabolism by Butane-Grown CF8, Pseudomonas butanovora, and Mycobacterium vaccae JOB5 and Methane-Grown Methylosinus trichosporium OB3b

    PubMed Central

    Hamamura, N.; Page, C.; Long, T.; Semprini, L.; Arp, D. J.

    1997-01-01

    Chloroform (CF) degradation by a butane-grown enrichment culture, CF8, was compared to that by butane-grown Pseudomonas butanovora and Mycobacterium vaccae JOB5 and to that by a known CF degrader, Methylosinus trichosporium OB3b. All three butane-grown bacteria were able to degrade CF at rates comparable to that of M. trichosporium. CF degradation by all four bacteria required O(inf2). Butane inhibited CF degradation by the butane-grown bacteria, suggesting that butane monooxygenase is responsible for CF degradation. P. butanovora required exogenous reductant to degrade CF, while CF8 and M. vaccae utilized endogenous reductants. Prolonged incubation with CF resulted in decreased CF degradation. CF8 and P. butanovora were more sensitive to CF than either M. trichosporium or M. vaccae. CF degradation by all three butane-grown bacteria was inactivated by acetylene, which is a mechanism-based inhibitor for several monooxygenases. Butane protected all three butane-grown bacteria from inactivation by acetylene, which indicates that the same monooxygenase is responsible for both CF and butane oxidation. CF8 and P. butanovora were able to degrade other chlorinated hydrocarbons, including trichloroethylene, 1,2-cis-dichloroethylene, and vinyl chloride. In addition, CF8 degraded 1,1,2-trichloroethane. The results indicate the potential of butane-grown bacteria for chlorinated hydrocarbon transformation. PMID:16535693

  7. Environmental implications of soil remediation using the Fenton process.

    PubMed

    Villa, Ricardo D; Trovó, Alam G; Nogueira, Raquel F Pupo

    2008-03-01

    This work evaluates some collateral effects caused by the application of the Fenton process to 1,1-bis(4-chlorophenyl)-2,2,2-trichloroethane (DDT) and diesel degradation in soil. While about 80% of the diesel and 75% of the DDT present in the soil were degraded in a slurry system, the dissolved organic carbon (DOC) in the slurry filtrate increased from 80 to 880mgl(-1) after 64h of reaction and the DDT concentration increased from 12 to 50microgl(-1). Experiments of diesel degradation conducted on silica evidenced that soluble compounds were also formed during diesel oxidation. Furthermore, significant increase in metal concentrations was also observed in the slurry filtrate after the Fenton treatment when compared to the control experiment leading to excessive concentrations of Cr, Ni, Cu and Mn according to the limits imposed for water. Moreover, 80% of the organic matter naturally present in the soil was degraded and a drastic volatilization of DDT and 2,2-bis(4-chlorophenyl)-1,1-dichloroethylene was observed. Despite the high percentages of diesel and DDT degradation in soil, the potential overall benefits of its application must be evaluated beforehand taking into account the metal and target compounds dissolution and the volatilization of contaminants when the process is applied. PMID:18068206

  8. Effect of Fe(III) on 1,1,2,2-tetrachloroethane degradation and vinyl chloride accumulation in wetland sediments of the Aberdeen proving ground

    USGS Publications Warehouse

    Jones, E.J.P.; Voytek, M.A.; Lorah, M.M.

    2004-01-01

    1,1,2,2-Tetrachloroethane (TeCA) contaminated groundwater at the Aberdeen Proving Ground discharges through an anaerobic wetland in West Branch Canal Creek, MD, where dechlorination occurred. Two microbially mediated pathways, dichloroelimination and hydrogenolysis, account for most of the TeCA degradation at this site. The dichloroelimination pathways led to the formation of vinyl chloride (VC), a recalcitrant carcinogen of great concern. The effect of adding Fe(III) to TeCA-amended microcosms of wetland sediment was studied. Differences were identified in the TeCA degradation pathway between microcosms treated with amorphous ferric oxyhydroxide (AFO-treated) and untreated (no AFO) microcosms. TeCA degradation was accompanied by a lower accumulation of VC in AFO-treated microcosms than no AFO microcosms. The microcosm incubations and subsequent experiments with the microcosm materials showed that AFO treatment resulted in lower production of VC by shifting TeCA degradation from dichloroelimination pathways to production of a greater proportion of chlorinated ethane products, and decreasing the microbial capability to produce VC from 1,2-dichloroethylene. VC degradation was not stimulated in the presence of Fe(III). Rather, VC degradation occurred readily under methanogenic conditions and was inhibited under Fe(III)-reducing conditions.

  9. Development and composition of a mixed culture for bioremediation of chlorinated ethenes and ethanes

    USGS Publications Warehouse

    Jones, E.J.P.; Voytek, M.A.; Lorah, M.M.

    2005-01-01

    Microbial organisms capable of dechlorinating 1,1,2,2 tetrachloroethane (TeCA) and its chlorinated ethane and ethylene daughter products were enriched in surface sediments collected from the West Branch Canal Creek wetland area, leading to the formation of two mixed cultures using slightly different enrichment methods. Both WBC-1 and WBC-2 were capable of rapid and complete reductive dechlorination of TeCA and its daughter products (1,1,2-trichloroethane, 1,2-dichloroethane, trichloroethylene, 1,2-dichloroethylene, and vinyl chloride) to ethylene, and addition of either culture to wetland sediment and to engineered peat/compost mixtures resulted in significant enhancement of dechlorination. However, the WBC-2 culture supported better sustained activity and was more readily scaled up for application in bioaugmentation treatments, whereas dechlorination activity was gradually lost in WBC-1. The microbial composition of WBC-1 and WBC-2 were determined by cloning and sequencing 500 base pairs of the 16S rDNA gene and the methyl co-reductase. Methanogens identified in the consortia were members of the Order Methanomicrobiales, which includes acetoclastic methanogens. This is an abstract of a paper presented at the Proceedings of the 8th International In Situ and On-Site Bioremediation Symposium (Baltimore, MD 6/6-9/2005).

  10. Global pollution monitoring of PCBs and organochlorine pesticides using skipjack tuna as a bioindicator.

    PubMed

    Ueno, D; Takahashi, S; Tanaka, H; Subramanian, A N; Fillmann, G; Nakata, H; Lam, P K S; Zheng, J; Muchtar, M; Prudente, M; Chung, K H; Tanabe, S

    2003-10-01

    Concentrations of organochlorines (OCs) representing persistent organic pollutants (POPs), such as polychlorinated biphenyls (PCBs), dichlorodiphenyl trichloroethane and its metabolites (DDTs), chlordane compounds (CHLs), hexachlorocyclohexane isomers (HCHs), and hexachlorobenzene (HCB), were determined in the liver of skipjack tuna (Katsuwonus pelamis) collected from the offshore waters of various regions in the world (offshore waters around Japan, Taiwan, Philippines, Indonesia, Seychelles, and Brazil, and the Japan Sea, the East China Sea, the South China Sea, the Bay of Bengal, and the North Pacific Ocean). OCs were detected in livers of all of the skipjack tuna collected from the locations surveyed, supporting the thesis that there is widespread contamination of persistent OCs in the marine environment. Within a location, no significant relationship between growth-stage (body length and weight) and OC concentrations (lipid weight basis) was observed, and the OC residue levels were rather uniform among the individuals. Interestingly, the distribution of OC concentrations in skipjack tuna was similar to those in surface seawaters from which they were taken. These results suggest that OC concentrations in skipjack tuna could reflect the pollution levels in seawater from which they are collected and that this species is a suitable bioindicator for monitoring the global distribution of OCs in offshore waters and the open ocean. Concentrations of PCBs and CHLs in skipjack tuna were higher in offshore waters around Japan (up to 1100 and 250 ng/g lipid wt, respectively), suggesting the presence of sources of PCBs and CHLs in Japan. High concentrations of DDTs and HCHs were observed in samples from the Japan Sea, the East China Sea, the South China Sea, and the Bay of Bengal (up to 1300 and 22 ng/g lipid wt, respectively). This result suggests recent use of technical DDT and HCH for agricultural and/or public health purposes in Russia, China, India, and some other

  11. Synthesis and characterization of sulfonated poly (arylene ether sulfone) copolymers via direct copolymerization: Candidates for proton exchange membrane fuel cells

    NASA Astrophysics Data System (ADS)

    Harrison, William Lamont

    A designed series of directly copolymerized homo- and disulfonated copolymers containing controlled degrees of pendant sulfonic acid groups have been synthesized via nucleophilic step polymerization. Novel sulfonated poly (arylene ether sulfone) copolymers using 4,4'-bisphenol A, 4,4'-biphenol, hexafluorinated (6F) bisphenol AF, and hydroquinone, respectively, with dichlorodiphenyl sulfone (DCDPS) and 3,3'-disodiumsulfonyl-4,4'-dichlorodiphenylsulfone (SDCDPS) were investigated. Molar ratios of DCDPS and SDCDPS were systematically varied to produce copolymers of controlled compositions, which contained up to 70 mol% of disulfonic acid moiety. The goal is to identify thermally, hydrolytically, and oxidatively stable high molecular weight, film-forming, ductile ion conducting copolymers, which had properties desirable for proton exchange membranes (PEM) in fuel cells. Commercially available bisphenols were selected to produce cost effective alternative PEMs. Partially aliphatic bisphenol A and hexafluorinated (6F) bisphenol AF produced amorphous copolymers with different thermal oxidative and surface properties. Biphenol and hydroquinone was utilized to produce wholly aromatic copolymers. The sulfonated copolymers were prepared in the sodium-salt form and converted to the acid moiety via two different methodologies and subsequently investigated as proton exchange membranes for fuel cells. Hydrophilicity increased with the level of disulfonation, as expected. Moreover, water sorption increased with increasing mole percent incorporation of SDCDPS. The copolymers' water uptake was a function of both bisphenol structure and degree of disulfonation. Furthermore, the acidification procedures were shown to influence the Tg values, water uptake, and conductivity of the copolymers. Atomic force microscopy (AFM) in the tapping mode confirmed that the morphology of the copolymers could be designed to display nanophase separation in the hydrophobic and hydrophilic (sulfonated

  12. Pre-Pregnancy Maternal Exposure to Persistent Organic Pollutants and Gestational Weight Gain: A Prospective Cohort Study.

    PubMed

    Jaacks, Lindsay M; Boyd Barr, Dana; Sundaram, Rajeshwari; Grewal, Jagteshwar; Zhang, Cuilin; Buck Louis, Germaine M

    2016-01-01

    Persistent organic pollutants (POPs) have been implicated in the development of obesity in non-pregnant adults. However, few studies have explored the association of POPs with gestational weight gain (GWG), an important predictor of future risk of obesity in both the mother and offspring. We estimated the association of maternal pre-pregnancy levels of 63 POPs with GWG. Data are from women (18-40 years; n = 218) participating in a prospective cohort study. POPs were assessed using established protocols in pre-pregnancy, non-fasting blood samples. GWG was assessed using three techniques: (1) total GWG (difference between measured pre-pregnancy weight and final self-reported pre-delivery weight); (2) category based on pre-pregnancy body mass index (BMI)-specific Institute of Medicine (IOM) recommendations; and (3) area under the GWG curve (AUC). In an exploratory analysis, effects were estimated separately for women with BMI < 25 kg/m² versus BMI ≥ 25 kg/m². Multivariable polytomous logistic regression and linear regression were used to estimate the association between each chemical or congener and the three GWG outcomes. p,p'-dichlorodiphenyl trichloroethane (p,p'-DDT) was significantly inversely associated with AUC after adjustment for lipids and pre-pregnancy BMI: beta {95% confidence interval (CI)}, -378.03 (-724.02, -32.05). Perfluorooctane sulfonate (PFOS) was significantly positively associated with AUC after adjustment for lipids among women with a BMI < 25 kg/m² {beta (95% CI), 280.29 (13.71, 546.86)}, but not among women with a BMI ≥ 25 kg/m² {beta (95% CI), 56.99 (-328.36, 442.34)}. In summary, pre-pregnancy levels of select POPs, namely, p,p'-DDT and PFOS, were moderately associated with GWG. The association between POPs and weight gain during pregnancy may be more complex than previously thought, and adiposity prior to pregnancy may be an important effect modifier. PMID:27626435

  13. Biomonitoring of Environmental Status and Trends (BEST) Program: Environmental Contaminants, Health Indicators, and Reproductive Biomarkers in Fish from the Mobile, Apalachicola-Chattahoochee-Flint, Savannah, and Pee Dee River Basins

    USGS Publications Warehouse

    Hinck, Jo Ellen; Blazer, Vicki; Denslow, Nancy D.; Echols, Kathy R.; Gale, Robert W.; May, Tom W.; Claunch, Rachael; Wieser, Carla; Anderson, Patrick J.; Coyle, James J.; Gross, Timothy S.; Tillitt, Donald E.

    2007-01-01

    Largemouth bass (Micropterus salmoides) and common carp (Cyprinus carpio) were collected from 13 sites in 4 river basins in the southeastern United States to document spatial trends in accumulative contaminants, health indicators, and reproductive biomarkers. Organochlorine residues, 2,3,7,8- tetrachlorodibenzo-p-dioxin-like activity (TCDD-EQ), and elemental contaminants were measured in composite samples of whole fish, grouped by species and gender, from each site. Fish were field-examined for external and internal anomalies, selected organs were weighed to compute somatic indices, and tissue and fluid samples were preserved for fish health and reproductive biomarker analyses. Mercury concentrations in bass samples from all sites exceeded toxicity thresholds for mammals [>0.1 micrograms per gram wet weight (ug/g ww)], fish (>0.2 ug/g ww), and birds (>0.3 ug/g ww) and were greatest (>0.5 ug/g ww) in samples from the Alabama River at Eureka Landing, Alabama; the Mobile River at Bucks, Alabama; the Apalachicola River at Blountstown, Florida; the Savannah River at Sylvania, Georgia; and the Pee Dee River at Bucksport, South Carolina. Selenium concentrations were relatively high (>0.75 ug/g ww) in fish from the Tombigbee River at Lavaca, Alabama; the Mobile River at Bucks; and the Chattahoochee River at Omaha, Georgia compared to those from other sites. Concentrations of 2,2-bis (p-chlorophenyl)- 1,1-dichloroethylene (p,p'-DDE) were high in fish from the Chattahoochee River at Omaha and the Mobile River near Bucks, which was near a 2,2-bis (p-chlorophenyl)-1,1- dichloroethylene (DDT) formulating facility that historically discharged into the lower Mobile River. Toxaphene concentrations in fish from the Flint River near Albany, Georgia (60-100 nanograms per gram (ng/g) ww) may pose a risk to fish. Concentrations of other formerly used (total chlordanes, dieldrin, endrin, aldrin, mirex, and hexachlorobenzene) and currently used (pentachlorobenzene, pentachloroanisole

  14. An assessment of natural biotransformation of petroleum hydrocarbons and chlorinated solvents at an aquifer plume transect.

    PubMed

    Skubal, K L; Barcelona, M J; Adriaens, P

    2001-05-01

    Field biogeochemical characterization and laboratory microcosm studies were performed to assess the potential for future biotransformation of trichloroethylene (TCE) and toluene in a plume containing petroleum hydrocarbons and chlorinated solvents at the former Wurtsmith Air Force Base in Oscoda, MI. In situ terminal electron accepting processes (TEAPs), contaminant composition and microbial phylogeny were studied at a plume transect 100 m downgradient of the source. The presence of reduced electron acceptors, relevant microbial communities, and elevated dissolved methane and carbon dioxide concentrations at the transect, as well as downgradient accumulation of BTEX metabolites and dechlorination products, indicated that past or current reductive dechlorination at the transect was likely driven by BTEX biodegradation in the methanogenic zone. However, TCE and toluene mineralization in sediment-groundwater microcosms without added electron acceptors did not exceed 5% during 300 days of incubation and was nearly invariant with original sediment TEAP, even following amendments of nitrogen and phosphorus. Mineralization rates were on the order of 0.0015-0.03 mumol/g day. After 8 months, microcosms showed evidence of methanogenesis, but CH4 and CO2 production arose from the degradation of contaminants other than toluene. Cis-dichloroethylene was observed in only one methanogenic microcosm after more than 500 days. It appears likely that spatially and temporally dynamic redox zonation at the plume transect will prevent future sustained reductive dehalogenation of highly chlorinated solvents, for during the course of a year, the predominant TEAP at the highly contaminated water table shifted from methanogenesis to iron- and sulfate-reduction. It is recommended that biotransformation studies combine considerations of long-term, spatially relevant changes in redox zonation with laboratory-scale studies of electron donor utilization and cometabolic substrate transformation

  15. Development of a simple, accurate SPME-based method for assay of VOCs in column breakthrough experiments.

    PubMed

    Salaices Avila, Manuel Alejandro; Breiter, Roman; Mott, Henry

    2007-01-01

    Solid-phase microextraction (SPME) with gas chromatography is to be used for assay of effluent liquid samples from soil column experiments associated with VOC fate/transport studies. One goal of the fate/transport studies is to develop accurate, highly reproducible column breakthrough curves for 1,2-cis-dichloroethylene (cis-DCE) and trichloroethylene (TCE) to better understand interactions with selected natural solid phases. For SPME, the influences of the sample equilibration time, extraction temperature and the ratio of volume of sample bottle to that of the liquid sample (V(T)/V(w)) are the critical factors that could influence accuracy and precision of the measured results. Equilibrium between the gas phase and liquid phase was attained after 200 min of equilibration time. The temperature must be carefully controlled due to variation of both the Henry's constant (K(h)) and the fibre/gas phase distribution coefficient (K(fg)). K(h) decreases with decreasing temperature while K(fg) increases. Low V(T)/V(w) yields better sensitivity but results in analyte losses and negative bias of the resultant assay. High V(T)/V(w) ratio yields reduced sensitivity but analyte losses were found to be minimal, leading to better accuracy and reproducibility. A fast SPME method was achieved, 5 min for SPME extraction and 3.10 min for GC analysis. A linear calibration function in the gas phase was developed to analyse the breakthrough curve data, linear between a range of 0.9-236 microgl(-1), and a detection limit lower than 5 microgl(-1). PMID:16844196

  16. Abiotic reductive dechlorination of chlorinated ethylenes by iron-bearing phyllosilicates.

    PubMed

    Lee, Woojin; Batchelor, Bill

    2004-09-01

    Abiotic reductive dechlorination of chlorinated ethylenes (tetrachloroethylene (PCE), trichloroethylene (TCE), cis-dichloroethylene (c-DCE), and vinylchloride (VC)) by iron-bearing phyllosilicates (biotite, vermiculite, and montmorillonite) was characterized to obtain better understanding of the behavior of these contaminants in systems undergoing remediation by natural attenuation and redox manipulation. Batch experiments were conducted to evaluate dechlorination kinetics and some experiments were conducted with addition of Fe(II) to simulate impact of microbial iron reduction. A modified Langmuir-Hinshelwood kinetic model adequately described reductive dechlorination kinetics of target organics by the iron-bearing phyllosilicates. The rate constants stayed between 0.08 (+/-10.4%) and 0.401 (+/-8.1%) day(-1) and the specific initial reductive capacity of iron-bearing phyllosilicates for chlorinated ethylenes stayed between 0.177 (+/-6.1%) and 1.06 (+/-7.1%) microM g(-1). The rate constants for the reductive dechlorination of TCE at reactive biotite surface increased as pH (5.5-8.5) and concentration of sorbed Fe(II) (0-0.15 mM g(-1)) increased. The appropriateness of the model is supported by the fact that the rate constants were independent of solid concentration (0.0085-0.17 g g(-1)) and initial TCE concentration (0.15-0.60 mM). Biotite had the greatest rate constant among the phyllosilicates both with and without Fe(II) addition. The rate constants were increased by a factor of 1.4-2.5 by Fe(II) addition. Between 1.8% and 36% of chlorinated ethylenes removed were partitioned to the phyllosilicates. Chloride was produced as a product of degradation and no chlorinated intermediates were observed throughout the experiment. PMID:15268967

  17. Stable carbon isotope fractionation during aerobic biodegradation of chlorinated ethenes

    SciTech Connect

    Chu, Kung-Hui; Mahendra, Shaily; Song, Donald L.; Conrad, Mark E.; Alvarez-Cohen, Lisa

    2003-06-01

    Stable isotope analysis is recognized as a powerful tool for monitoring, assessing, and validating in-situ bioremediation processes. In this study, kinetic carbon isotope fractionation factors () associated with the aerobic biodegradation of vinyl chloride (VC), cis-1,2-dichloroethylene (cDCE), and trichloroethylene (TCE) were examined. Of the three solvents, the largest fractionation effects were observed for biodegradation of VC. Both metabolic and cometabolic VC degradation were studied using Mycobacterium aurum L1 (grown on VC), Methylosinus trichosporium OB3b (grown on methane), Mycobacterium vaccae JOB 5 (grown on propane), and two VC enrichment cultures seeded from contaminated soils of Alameda Point and Travis Air Force Base, CA. M. aurum L1 caused the greatest fractionation (= -5.7) while for the cometabolic cultures, values ranged from -3.2 to -4.8. VC fractionation patterns for the enrichment cultures were within the range of those observed for the metabolic and cometabolic cultures (= -4.5 to -5.5). The fractionation for cometabolic degradation of TCE by Me. trichosporium OB3b was low (= -1.1), while no quantifiable carbon isotopic fractionation was observed during the cometabolic degradation of cDCE. For all three of the tested chlorinated ethenes, isotopic fractionation measured during aerobic degradation was significantly smaller than that reported for anaerobic reductive dechlorination. This study suggests that analysis of compound-specific isotopic fractionation could assist in determining whether aerobic or anaerobic degradation of VC and cDCE predominates in field applications of in-situ bioremediation. In contrast, isotopic fractionation effects associated with metabolic and cometabolic reactions are not sufficiently dissimilar to distinguish these processes in the field.

  18. Geohydrology and ground-water quality at the Pueblo Depot activity landfill near Pueblo, Colorado

    USGS Publications Warehouse

    Watts, Kenneth R.; Ortiz, Roderick F.

    1990-01-01

    Groundwater samples were collected from the shallow unconfined aquifer at the Pueblo Depot Activity (Colorado) landfill and downstream from the landfill. The Pueblo Depot Activity is a U.S. Department of the Army facility in southeastern Colorado about 15 miles east of Pueblo, Colorado. The land-fill is underlain by upland alluvial terrace deposits that overlie a thick and almost impermeable shale. Saturated thickness of the aquifer generally is from 5 to 10 feet. Groundwater flow at the landfill is to the south-southeast toward the Arkansas River valley. Though not hydraulically connected to the upland terrace deposits, the alluvium underlying the Arkansas River valley may be recharged by groundwater that is discharged from seeps at the contact of the upland terrace deposits and the Pierre Shale. The water is classified as a mixed-cation mixed-anion type water that has concentrations of dissolved solids of 710 to 1,810 mg/L. Dissolved-solids concentrations increase downgradient. Chemical analysis, done to determine possible contamination of the groundwater, indicated that concentrations of trichloroethylene ranged from 5.2 to 2,900 microg/L and of trans-1,2-dichloroethylene ranged from 5 to 720 microg/L. The areal distribution of these volatile organic compounds indicate that there possibly are two sources of contamination of groundwater at the landfill, one upgradient from the landfill and the other within the landfill. Analysis of water samples from wells and seeps offsite and downgradient from the landfill did not indicate either contaminant in groundwater from the alluvial aquifer underlying the Arkansas River valley. (USGS)

  19. Satellite telemetry and prey sampling reveal contaminant sources to Pacific Northwest Ospreys.

    PubMed

    Elliott, John E; Morrissey, Christy A; Henny, Charles J; Inzunza, Ernesto Ruelas; Shaw, Patrick

    2007-06-01

    Migratory behavior can be an important factor in determining contaminant exposure in avian populations. Accumulation of organochlorine (OC) pesticides while birds are wintering in tropical regions has been cited often as the reason for high concentrations in migrant populations. To explore this issue, we satellite tracked 16 Ospreys (Pandion haliaetus) over the period 1996-2003 from breeding sites in British Columbia, Canada, and integrated the results into a database on 15 Ospreys that were satellite tracked over the period 1995-1999, from breeding locations in Washington and Oregon, USA. Data on wintering sites of 31 Ospreys in Mexico and Central America were used for spatially targeted sampling of prey fish. Concentrations of the main organochlorine contaminant, p,p'-dichloro-diphenyl-dichloroethylene (DDE), in fish composites from Mexico ranged from 0.005 to 0.115 nicrog/g wet mass. Significant differences existed among fish families in p,p'-DDE, total dichloro-diphenyl-trichloroethane (sigmaDDT), sigmachlordanes, and total polychlorinated biphenyls (sigmaPCBs). Catfish (family Ariidae) generally had significantly higher levels of DDT metabolites and other organochlorine contaminants compared to other fish families collected. Differences in prey contaminant levels were detected among the collection sites around coastal Mexico, with fish from Veracruz State generally having higher levels of DDT metabolites, sigmachlordanes, sigmaPCBs, and hexachlorobenzene. Eggs collected from 16 nests throughout the Pacific Northwest (nine from British Columbia, seven from Oregon and Washington) where Ospreys had been satellite tagged, showed marked variation in levels of DDT metabolites (p,p'-DDE; range 0.02-10.14 microg/g). Wintering site had no significant effect on contaminant concentrations in sample eggs from those specific Ospreys; rather concentrations of p,p'-DDE, were predicted by breeding sites with highest levels in eggs of Ospreys breeding in the lower Columbia

  20. DDE, selenium, mercury, and white-faced IBIS reproduction at Carson Lake, Nevada

    SciTech Connect

    Henny, C.J. ); Herron, G.B. )

    1989-10-01

    We studied organochlorine, mercury (Hg), and selenium (Se) contamination in white-faced ibis (Plegadis chihi) nesting at Carson Lake, Nevada, in 1985 and 1986. Dichloro diphenyl dichloroethylene (DDE) was related to fewer young produced/nesting attempt, fewer young produced/successful nest and eggshell thinning. As DDE in eggs increase to >4ppm (wet wt), and especially >8ppm, productivity decreased significantly and the incidence of cracked eggs increased. Assuming that 4 ppm DDE is the critical residue level, 40% of the nesting population in 1985 and 1986 was adversely impacted by DDE, with a net loss of 20% of the poplation's expected production (to about 10 days old). Most eggs containing exceptionally high DDE levels (8-29 ppm) also had substantial amounts of dichloro diphenyl trichloroethane (DDT), which implies recently-used DDT as the source. No evidence of breeding ground DDE-DDT contamination was found. The white-faced ibis winter in Mexico, and mostly in the interior agricultural region. Concentration of DDE-DDT in ibis eggs, unlike most other wading bird species from the Great Basin, did not decline during the last decade. Other organochlorine contaminants were generally low and detected in {le}33% of the eggs. Selenium and Hg were accumulated by ibis on the Nevada breeding grounds, but concentrations in eggs did not reach levels sufficient to impact the production of 7-10 day old young. Potential Se and especially Hg accumulation during the remainder of the summer was high, but actual effects on growing young and adults remain unknown.

  1. Characterization of chemically modified enzymes for bioremediation-reactions. 1997 annual progress report

    SciTech Connect

    Kaufman, E.N.; Adams, M.W.W.

    1997-09-01

    'Many, if not most, biological transformation reactions of interest to US Department of Energy (DOE) site remediation involve substrates that are only sparingly soluble in aqueous environments. Hence, destruction of these recalcitrant and toxic materials would benefit tremendously if their degradation could be performed in nonaqueous environments. Organic biocatalysis may be motivated by the nature of the substrate itself, augmented mass transport, ease of product recovery, or novel reaction pathways afforded by the organic solvent. For instance, polychlorinated biphenyls (PCBs) are sparingly soluble in water, but may be more effectively processed when solubilized by organic liquids. However, naturally-occurring enzymes are not soluble in organic solvents. Indeed, most spontaneously denature and, depending on the solvent used, typically form inactive and insoluble precipitates. The objective of the current work is to gain a fundamental understanding of the molecular and catalytic properties of enzymes that have been chemically-modified so that they are catalytically-active and chemically-thermally-stable in organic solvents. The premise for this study is that highly stable enzymes which are catalytically active in both water and in a range of organic solvents are optimally suited for bioremediation where substrates of interest are more soluble and may be processed with greater specificity in nonaqueous solvents. The proposed research program will enable the development of nonaqueous bioremediation technologies for the treatment of DOE sites contaminated with aqueous-insoluble organic compounds. Such compounds may include dense nonaqueous phase liquids, trichloroethylene (TCE), trichloroacetic acid, trans-dichloroethylene, diesel fuel, and PCBs. These compounds have been identified as targets for technology development in the ``EM Technology Needs Database,'''' and are contaminants at the following DOE sites: K-25 Site plumes; ORNL WAGS 1, 4, and 5; Paducah plumes

  2. Mixed Pollutant Degradation by Methylosinus trichosporium OB3b Expressing either Soluble or Particulate Methane Monooxygenase: Can the Tortoise Beat the Hare?▿

    PubMed Central

    Lee, Sung-Woo; Keeney, David R.; Lim, Dong-Hee; Dispirito, Alan A.; Semrau, Jeremy D.

    2006-01-01

    Methanotrophs have been widely investigated for in situ bioremediation due to their ubiquity and their ability to degrade halogenated hydrocarbons through the activity of methane monooxygenase (MMO). It has been speculated that cells expressing the soluble form of MMO (sMMO) are more efficient in cleaning up sites polluted with halogenated hydrocarbons due to its broader substrate range and relatively fast degradation rates compared cells expressing the other form of MMO, the particulate MMO (pMMO). To examine this issue, the biodegradation of mixtures of chlorinated solvents, i.e., trichloroethylene (TCE), trans-dichloroethylene (t-DCE), and vinyl chloride (VC), by Methylosinus trichosporium OB3b in the presence of methane using either form of MMO was investigated over longer time frames than those commonly used, i.e., days instead of hours. Growth of M. trichosporium OB3b along with pollutant degradation were monitored and analyzed using a simple comparative model developed from the Ω model created for analysis of the competitive binding of oxygen and carbon dioxide by ribulose bisphosphate carboxylase. From these findings, it appears that at concentrations of VC, t-DCE, and TCE greater than 10 μM each, methanotrophs expressing pMMO have a competitive advantage over cells expressing sMMO due to higher growth rates. Despite such an apparent growth advantage, pMMO-expressing cells degraded less of these substrates at these concentrations than sMMO-expressing cells during active growth. If the concentrations were increased to 100 μM, however, not only did pMMO-expressing cells grow faster, they degraded more of these pollutants and did so in a shorter amount of time. These findings suggest that the relative rates of growth substrate and pollutant degradation are important factors in determining which form of MMO should be considered for pollutant degradation. PMID:17012599

  3. The effect of silica on the degradation of organohalides in granular iron columns

    NASA Astrophysics Data System (ADS)

    Kohn, Tamar; Lynn Roberts, A.

    2006-02-01

    Dissolved silica species are naturally occurring, ubiquitous groundwater constituents with corrosion-inhibiting properties. Their influence on the performance and longevity of iron-based permeable reactive barriers for treatment of organohalides was investigated through long-term column studies using Connelly iron as the reactive medium. Addition of dissolved silica (0.5 mM) to the column feed solution led to a reduction in iron reactivity of 65% for trichloroethylene (TCE), 74% for 1,1,2-trichloroethane (1,1,2-TCA), and 93% for 1,1,1-trichloroethane (1,1,1-TCA), compared to columns operated under silica-free conditions. Even though silica adsorption was a gradual process, the inhibitory effect was evident within the first week, with subsequent decreases in reactivity over 288 days being relatively minor. Lower concentrations of dissolved silica species (0.2 mM) led to a lesser decrease (70%) in iron reactivity toward 1,1,1-TCA. The presence of dissolved silica species produced a shift in TCE product distribution toward the more highly chlorinated product cis-dichloroethylene ( cis-DCE), although it did not appear to alter products originating from the trichloroethanes. The major corrosion products identified were magnetite (Fe 3O 4) or maghemite (γ-Fe 2O 3) and carbonate green rust ([Fe 42+Fe 23+(OH) 12][CO 3·2H 2O]). Iron carbonate hydroxide (Fe(II) 1.8Fe(III) 0.2(OH) 2.2CO 3) was only found in the silica-free column, indicating that silica may hinder its formation. A comparison with columns operated under the same conditions, but using Master Builder iron as the reactive matrix, showed that Connelly iron is initially less reactive, but performs better than Master Builder iron over 288 days.

  4. Metabolic and mutagenicity studies on DDT and 15 derivatives. Detection of 1,1-bis(p-chlorophenyl)-2,2-dichloroethane and 1,1-bis(p-chlorophenyl)-2,2,2-trichloroethyl acetate (kelthane acetate) as mutagens in Salmonella typhimurium and of 1,1-bis(p-chlorophenyl) ethylene oxide, a likely metabolite, as an alkylating agent.

    PubMed

    Planche, G; Croisy, A; Malaveille, C; Tomatis, L; Bartsch, H

    1979-05-01

    Using a novel in vitro technique, whereby microsomal enzymes were embedded in an agar layer to prolong their viability, 1,1-bis(p-chlorophenyl) ethylene(DDNU), a mammalian metabolite of 1,1-bis(p-chlorophenyl)-2,2,2-trichloroethane (DDT), was converted by microsomal mono-oxygenases of mouse liver into 1,1-bis(p-chlorophenyl)-1,2-ethanediol (DDNU-diol). The putative epoxide intermediate, 1,1-bis(p-chlorophenyl)ethylene oxide (DDNU-oxide), a new compound, was synthesized; it showed weak alkylating activity with 4-(4-nitrobenzyl)pyridine but was not mutagenic in Salmonella typhimurium strains TA100 and TA98. DDT and 13 of its metabolites or putative synthetic derivatives, including 1,1-bis(p-chlorophenyl)-2,2-dichloroethylene (DDE), 1 1,1-bis(p-chlorophenyl)-2-chloroethylene (DDMU), 1,1-bis(p-chlorophenyl)-2-chloroethane (DDMS)-DDNU, 2,2-bis(p-chlorophenyl)ethanol (DDOH), bis(p-chlorophenyl)acetic acid (DDA) and 1,1-bis(p-chlorophenyl)-2,2,2-trichloroethanol (Kethane), caused no mutagenic effects in S. typhimurium strains TA100 or TA98, either in the presence or absence of a mouse-liver microsomal fraction. 1,1-Bis(p-chlorophenyl)-2,2,2-trichloroethyl acetate (Kelthane acetate) was a direct-acting mutagen in strain TA100, whereas 1,1-bis(p-chlorophenyl)-2,2-dichloroethane (DDD) was mutagenic in TA98, only in the presence of a mouse-liver microsomal system. The results are discussed in relation to possible pathways whereby DDT is activated to mutagenic and/or carcinogenic metabolites. PMID:380827

  5. Potential of isotope analysis (C, Cl) to identify dechlorination mechanisms

    NASA Astrophysics Data System (ADS)

    Cretnik, Stefan; Thoreson, Kristen; Bernstein, Anat; Ebert, Karin; Buchner, Daniel; Laskov, Christine; Haderlein, Stefan; Shouakar-Stash, Orfan; Kliegman, Sarah; McNeill, Kristopher; Elsner, Martin

    2013-04-01

    Chloroethenes are commonly used in industrial applications, and detected as carcinogenic contaminants in the environment. Their dehalogenation is of environmental importance in remediation processes. However, a detailed understanding frequently accounted problem is the accumulation of toxic degradation products such as cis-dichloroethylene (cis-DCE) at contaminated sites. Several studies have addressed the reductive dehalogenation reactions using biotic and abiotic model systems, but a crucial question in this context has remained open: Do environmental transformations occur by the same mechanism as in their corresponding in vitro model systems? The presented study shows the potential to close this research gap using the latest developments in compound specific chlorine isotope analysis, which make it possible to routinely measure chlorine isotope fractionation of chloroethenes in environmental samples and complex reaction mixtures.1,2 In particular, such chlorine isotope analysis enables the measurement of isotope fractionation for two elements (i.e., C and Cl) in chloroethenes. When isotope values of both elements are plotted against each other, different slopes reflect different underlying mechanisms and are remarkably insensitive towards masking. Our results suggest that different microbial strains (G. lovleyi strain SZ, D. hafniense Y51) and the isolated cofactor cobalamin employ similar mechanisms of reductive dechlorination of TCE. In contrast, evidence for a different mechanism was obtained with cobaloxime cautioning its use as a model for biodegradation. The study shows the potential of the dual isotope approach as a tool to directly compare transformation mechanisms of environmental scenarios, biotic transformations, and their putative chemical lab scale systems. Furthermore, it serves as an essential reference when using the dual isotope approach to assess the fate of chlorinated compounds in the environment.

  6. Study on the kinetic characteristics of trace harmful gases for a two-person-30-day integrated CELSS test.

    PubMed

    Guo, Shuangsheng; Ai, Weidang; Fei, Jinxue; Xu, Guoxin; Zeng, Gu; Shen, Yunze

    2015-05-01

    A two-person-30-day controlled ecological life support system (CELSS) integrated test was carried out, and more than 30 kinds of trace harmful gases including formaldehyde, benzene, and ammonia were measured and analyzed dynamically. The results showed that the kinds and quantities of the trace harmful gases presented a continuously fluctuating state during the experimental period, but none of them exceed the spacecraft maximum allowable concentration (SMAC). The results of the Pre-Test (with two persons without plants for 3 days) and the Test (with two persons and four kinds of plants for 30 days) showed that there are some notable differences for the compositions of the trace harmful gases; the volatile organic compounds (VOCs) such as toluene, hexane, and acetamide were searched out in the Pre-Test, but were not found in the Test. Moreover, the concentrations of the trace harmful gases such as acetic benzene, formaldehyde, and ammonia decreased greatly in the Test more than those in the Pre-Test, which means that the plants can purify these gases efficiently. In addition, the VOCs such as carbon monoxide, cyclopentane, and dichloroethylene were checked out in the Test but none in the Pre-Test, which indicates that these materials might be from the crew's metabolites or those devices in the platform. Additionally, the ethylene released specially by plants accumulated in the later period and its concentration reached nearly ten times of 0.05 mg m(-3) (maximum allowed concentration for plant growth, which must have promoted the later withering of plants). We hoped that the work can play a referring function for controlling VOCs effectively so that future more CELSS integrating tests can be implemented smoothly with more crew, longer period, and higher closure. PMID:25483969

  7. Satellite telemetry and prey sampling reveal contaminant sources to pacific northwest ospreys

    USGS Publications Warehouse

    Elliott, J.E.; Morrissey, C.A.; Henny, C.J.; Inzunza, E.R.; Shaw, P.

    2007-01-01

    Migratory behavior can be an important factor in determining contaminant exposure in avian populations. Accumulation of organochlorine (OC) pesticides while birds are wintering in tropical regions has been cited often as the reason for high concentrations in migrant populations. To explore this issue, we satellite tracked 16 Ospreys (Pandion haliaetus) over the period 1996-2003 from breeding sites in British Columbia, Canada, and integrated the results into a database on 15 Ospreys that were satellite tracked over the period 1995-1999, from breeding locations in Washington and Oregon, USA. Data on wintering sites of 31 Ospreys in Mexico and Central America were used for spatially targeted sampling of prey fish. Concentrations of the main organochlorine contaminant, p,p???-dichloro-diphenyl-dichloroethylene (DDE), in fish composites from Mexico ranged from 0.005 to 0.115 ??g/g wet mass. Significant differences existed among fish families in p,p???-DDE, total dichloro- diphenyltrichloroethane (??DDT), ??chlordanes, and total polychlorinated biphenyls (??PCBs). Catfish (family Ariidae) generally had significantly higher levels of DDT metabolites and other organochlorine contaminants compared to other fish families collected. Differences in prey contaminant levels were detected among the collection sites around coastal Mexico, with fish from Veracruz State generally having higher levels of DDT metabolites, ??chlordanes, ??PCBs, and hexachlorobenzene. Eggs collected from 16 nests throughout the Pacific Northwest (nine from British Columbia, seven from Oregon and Washington) where Ospreys had been satellite tagged, showed marked variation in levels of DDT metabolites (p,p???-DDE; range 0.02-10.14 ??g/g). Wintering site had no significant effect on contaminant concentrations in sample eggs from those specific Ospreys; rather concentrations of p,p???-DDE, were predicted by breeding sites with highest levels in eggs of Ospreys breeding in the lower Columbia River

  8. Oxidative degradation and kinetics of chlorinated ethylenes by potassium permanganate

    NASA Astrophysics Data System (ADS)

    Yan, Y. Eugene; Schwartz, Frank W.

    1999-04-01

    The oxidative treatment of chlorinated ethylenes in ground water using permanganate was investigated in a series of batch kinetic tests. Five chlorinated ethylenes including tetrachloroethylene (PCE), trichloroethylene (TCE), and three isomers of dichloroethylenes (DCEs) were examined. The degradation process was rapid with pseudo-first-order rate constants ranging from 4.5×10 -5 to 0.03 s -1 at MnO 4-=1 mM. The rate increased with a decreasing number of chlorine substituents on the ethylene. The higher reactivity of trans-DCE ( kobs=30×10 -3 s -1 at MnO 4-=1 mM) as compared to cis-DCE ( kobs=0.9×10 -3 s -1 at MnO 4-=1 mM) is thought to be caused by a significant steric effect due to the formation of a large cyclic activated complex. TCE oxidation as a second-order reaction was confirmed and the rate constant, k=0.67±0.03 M -1 s -1, is independent of pH over the range of 4-8. The activity of both Cl - and hydrogen ions was monitored over time and suggests essentially complete dechlorination, making the degradation products less harmful than the parent compounds. Competition for MnO 4- from other organic compounds in ground water or highly contaminated ground water was also evaluated in experiments. A simple and quick approach was demonstrated to estimate permanganate consumption by other organic compounds for field applications and to predict the TCE degradation rate in a system involving multiple contaminants. The modeling results suggest that the effect of autocatalysis by MnO 2 on TCE degradation is significant when the system contains high concentration levels of MnO 4- and TOC.

  9. Dechlorination of perchloroethylene using zero-valent metal and microbial community

    NASA Astrophysics Data System (ADS)

    Ma, Changwen; Wu, Yanqing

    2008-07-01

    This research evaluates an integrated technique for the degradation of perchloroethylene (PCE) using a combination of zero-valent metal and an anaerobic microbial community. The microbial community was obtained from river sediment through a series of cultivation and enrichment processes, and was able to successfully convert PCE to ethylene. The degradation tests were carried out in five groups of reactors, i.e. Zn (zero-valent zinc), Fe (zero-valent iron), MB (a microbial community), ZnMB (zinc and a microbial community) and FeMB (iron and a microbial community). The results suggested that the FeMB system had the highest efficiency in removing PCE (about 99.9% after 24 days), followed by Zn (98.5%), ZnMB (84.8%), Fe (76.9%) and MB (49.6%). The degradation kinetics of PCE could be described by a pseudo-first-order reaction; the apparent reaction rate constants were 0.231, 0.187, 0.135, 0.076, 0.031 days-1 for the Zn, FeMB, ZnMB, Fe, and MB systems, respectively. Much more Cl- was detected as a by-product in the degradation tests using FeMB or ZnMB than using Fe or Zn. The results implied that not only PCE, but also the reaction intermediates, e.g., trichloroethylene (TCE) and dichloroethylenes (DCE isomers) may have been dechlorinated in the FeMB and ZnMB systems. Results suggest that the presence of the microbial community in the FeMB and ZnMB systems may not only affect the removal efficiency of PCE, but can also change the reaction pathways in the dechlorination process. The integrated technique combining the iron and the microbial community showed better degradation efficiency than the others; it may be viewed as an environmentally desirable remediation.

  10. Natural attenuation of trichloroethylene in fractured shale bedrock.

    PubMed

    Lenczewski, M; Jardine, P; McKay, L; Layton, A

    2003-07-01

    This paper describes one of the first well-documented field examples of natural attenuation of trichloroethylene (TCE) in groundwater in a fractured shale bedrock. The study was carried out adjacent to a former waste burial site in Waste Area Grouping 5 (WAG5) on the Oak Ridge Reservation, Oak Ridge, TN. A contaminant plume containing TCE and its daughter products were detected downgradient from the buried waste pits, with most of the contamination occurring in the upper 6 m of the bedrock. The monitoring well array consists of a 35-m-long transect of multilevel sampling wells, situated along a line between the waste pits and a seep which discharges into a small stream. Concentrations of volatile organic carbons (VOCs) were highest in the waste trenches and decreased with distance downgradient towards the seep. Sampling wells indicated the presence of overlapping plumes of TCE, cis-dichloroethylene (cDCE), vinyl chloride (VC), ethylene, ethane, and methane, with the daughter products extending further downgradient than the parent (TCE). This type of distribution suggests anaerobic biodegradation. Measurements of redox potential at the site indicated that iron-reduction, sulfate reduction, and potentially methanogensis were occurring and are conducive to dechlorination of TCE. Bacteria enrichment of groundwater samples revealed the presence of methanotrophs, methanogens, iron-reducing bacteria and sulfate-reducing bacteria, all of which have previously been implicated in anaerobic biodegradation of TCE. 16S rDNA sequence from DNA extracted from two wells were similar to sequences of organisms previously implicated in the anaerobic biodegradation of chlorinated solvents. The combined data strongly suggest that anaerobic biodegradation of the highly chlorinated compounds is occurring. Aerobic biodegradation may also be occurring in oxygenated zones, including near a seep where groundwater exits the site, or in the upper bedrock during seasonal fluctuations in water

  11. Long-term performance monitoring for a permeable reactive barrier at the U.S. Coast Guard Support Center, Elizabeth City, North Carolina.

    PubMed

    Puls, R W; Blowes, D W; Gillham, R W

    1999-08-12

    A continuous hanging iron wall was installed in June, 1996, at the U. S. Coast Guard (USCG) Support Center near Elizabeth City, NC, United States, to treat overlapping plumes of chromate and chlorinated solvent compounds. The wall was emplaced using a continuous trenching machine whereby native soil and aquifer sediment was removed and the iron simultaneously emplaced in one continuous excavation and fill operation. To date, there have been seven rounds (November 1996, March 1997, June 1997, September 1997, December 1997, March 1998, and June 1998) of performance monitoring of the wall. At this time, this is the only full-scale continuous 'hanging' wall installed as a permeable reactive barrier to remediate both chlorinated solvent compounds and chromate in groundwater. Performance monitoring entails the following: sampling of 10-5 cm PVC compliance wells and 15 multi-level samplers for the following constituents: TCE, cis-dichloroethylene (c-DCE), vinyl chloride, ethane, ethene, acetylene, methane, major anions, metals, Cr(VI), Fe(II), total sulfides, dissolved H(2), Eh, pH, dissolved oxygen, specific conductance, alkalinity, and turbidity. Electrical conductivity profiles have been conducted using a Geoprobe to verify emplacement of the continuous wall as designed and to locate upgradient and downgradient wall interfaces for coring purposes. Coring has been conducted in November, 1996, in June and September, 1997, and March, 1998, to evaluate the rate of corrosion on the iron surfaces, precipitate buildup (particularly at the upgradient interface), and permeability changes due to wall emplacement. In addition to several continuous vertical cores, angled cores through the 0.6-m thick wall have been collected to capture upgradient and downgradient wall interfaces along approximate horizontal flow paths for mineralogic analyses. PMID:10518667

  12. Removing hexavalent chromium from subsurface waters with anion-exchange resin

    SciTech Connect

    Torres, R.A.

    1995-06-01

    Some subsurface waters at Lawrence Livermore National Laboratory (LLNL) are contaminated with volatile organic compounds (VOCs). Hexavalent chromium, Cr(VI), is also present in the ground water; however, the source of the Cr(VI) may be natural. The Cr(VI) still must be treated if brought to the surface because its concentration exceeds discharge standards. We are planning facilities for removing the VOCs and Cr(VI) to a level below the discharge standards. The planned treatment includes the following steps: (1) Pumping the water to the surface facility. (2) Purging the VOCs with air and absorbing them on activated carbon. The VOCs in LLNL`s subsurface waters are primarily chlorinated organic solvents, such as dichloroethylene (DCE), trichloroethylene (TCE), perchloroethylene (PCE), and chloroform (CHCl{sub 3}). Contamination levels range from tens to thousands of parts per billion. (3) Filtering the water. (4) Passing the water through anion-exchange resin to remove the Cr. The Cr in LLNL subsurface waters occurs almost entirely as Cr(VI), which exists as the chromate anion, CrO{sub 4}{sup 2-}, at environmental pH. Cr levels range from tens to hundreds of parts per billion. (5) Discharging the treated water into the local arroyos. The relevant discharge criteria are 5 ppb total VOCs, 11 ppb Cr(VI), and pH between 6.5 and 8.5, inclusive. This report describes laboratory experiments undertaken to learn how the proposed treatment facility can be expected to operate. The laboratory results are expected to supply vendors with the detailed performance specifications needed to prepare bids on the Cr removal portion of the treatment facility. The treatment facility is expected to process 60 gallons per minute (gpm) of water by stripping VOCs with 720 standard cubic feet per minute (scfm) of air and removing Cr(VI) with 60 ft{sup 3} of resin.

  13. Treatment of chlorinated solvents by nitrogen-fixing and nitrate-supplied methane oxidizers in columns packed with unsaturated porous media

    SciTech Connect

    Chu, K.H.; Alvarez-Cohen, L.

    2000-05-01

    This study compares the feasibility of employing nitrogen-fixing and nitrate-supplied methane-oxidizing cultures grown in unsaturated porous media to degrade cis-1,2-dichloroethylene (cDCE) and trichloroethylene (TCE) in gas streams. Both nitrate-supplied and nitrogen-fixing columns degraded TCE completely at a gaseous concentration of 0.7 mg/L for 8--10 days. However, when columns were supplied with 4% CH{sub 4} and 10% O{sub 2}, nitrate-supplied columns were not able to recover after degrading TCE at a gaseous concentration of 0.13 mg/L for 7 days. In contrast, nitrogen-fixing columns recovered after degrading 0.13--0.4 mg/L TCE for 3--10 days and were capable of repeatedly degrading TCE at gaseous concentrations of 0.03--0.14 mg/L TCE for 3--10 days and were capable of repeatedly degrading TCE at gaseous concentrations of 0.03--0.14 mg/L during long-term intermittent operation that was punctuated by appropriate microbial recovery periods. Both nitrate-supplied and nitrogen-fixing columns were capable of degrading cDCE at concentrations of 0.7--1.0 mg/L for 5--10 days, but only the nitrogen-fixing columns recovered from cDCE exposure. The operating period for columns treating a mixture of TCE and cDCE was significantly shorter than that for treatment of TCE or cDCE alone. Several operating curves were developed to facilitate comparisons between operating conditions and to aid in predicting chlorinated solvent removals in such systems. Nitrogen-fixing columns consistently outperformed nitrate-supplied columns, and columns inoculated with a mixed culture outperformed those inoculated with Methylosinus trichosporium OB3b for TCE removal but not for cDCE removal.

  14. Environmental polychlorinated biphenyls: acute toxicity of landfill soil extract to female prepubertal rats.

    PubMed

    Hansen, L G; Li, M H; Saeed, A; Bush, B

    1995-10-01

    Subsurface soil from a National Priorities List landfill containing about 2.5% polychlorinated biphenyls (PCBs) was extracted and the extract cleaned by Florisil slurry and alumina column chromatography. The refined extract contained 48 mg/mL PCB, mainly trichlorobiphenyls and tetrachlorobiphenyls, traces of polychlorinated naphthalenes, 125 micrograms/mL 2,2-bis-p-chlorophenyl-1,1-dichloroethylene (DDE), and low levels of chlorinated dibenzofurans. The refined extract was dissolved in corn oil and administered intraperitoneally to weanling (day 20) female rats on days 20 and 21; rats were terminated on day 22. Limited data indicated possible hematopoietic effects, including neutrophilia. There were no changes in relative uterus, kidney, or adrenal gland weights between total doses of 3 to 96 mg/kg total PCB. Relative liver weights increased significantly at 36 mg/kg and activities of P450s 1A1 (as ethoxyresorufin O-dealkylase) and 2B (as pentoxyresorufin O-dealkylase) increased at 12 mg/kg and plateaued at 36 (P450 1A1) or 48 (P450 2b) mg/kg. Serum total thyroxine (T4) declined significantly at doses of 36 mg/kg and greater; thyroid follicular epithelial cells were significantly larger within the same dose range, but the follicular colloid area decreased to less than 60% control values at 12 mg/kg and remained at this size through 72 mg/kg. Maximum mobilization of T4 apparently occurred at 12 mg/kg and attenuated measured declines in circulating levels. Even though a large proportion of proven and probable estrogenic chlorobiphenyls (CBs) were present, the lower amounts of more potent antiestrogenic aryl hydrocarbon (Ah) receptor agonists and/or decreased responsiveness because of low serum T4 levels may have antagonized the uterotropic response. PMID:7487157

  15. Spatial distribution of organochlorine contaminants in soil, sediment, and fish in Bikini and Enewetak Atolls of the Marshall Islands, Pacific Ocean.

    PubMed

    Wang, Jun; Caccamise, Sarah A L; Wu, Liejun; Woodward, Lee Ann; Li, Qing X

    2011-08-01

    Several nuclear tests were performed at Enewetak and Bikini Atolls in the Marshall Islands between 1946 and 1958. The events at Bikini Atoll involved several ships that were tested for durability during nuclear explosions, and 24 vessels now rest on the bottom of the Bikini lagoon. Nine soil samples were collected from different areas on the two islands of the atoll, and eighteen sediment, nine fish, and one lobster were collected in the vicinity of the sunken ships. Organochlorine pesticides (OCPs), polychlorinated biphenyls (PCBs), and polychlorinated terphenyls (PCTs) in these samples were analyzed using gas chromatography/ion trap mass spectrometry (GC/ITMS). The average recoveries ranged from 78% to 104% for the different PCB congeners. The limits of detection (LOD) for PCBs, PCTs, DDE, DDT, and dieldrin ranged 10-50 pg g(-1). Some fish from Enewetak contained PCBs at a concentration range of 37-137 ng g(-1), dry weight (dw), and most of the soils from Enewetak showed evidence of PCBs (22-392 ng g(-1)dw). Most of the Bikini lagoon sediment samples contained PCBs, and the highest was the one collected from around the Saratoga, an aircraft carrier (1555 ng g(-1)dw). Some of the fish samples, most of the soil samples, and only one of the sediment samples contained 2,2-bis(4-chlorophenyl)-1,1-dichloroethylene (DDE) and PCBs. In addition to PCBs, the soils from Enewetak Atoll contained PCTs. PCTs were not detected in the sediment samples from Bikini Atoll. The results suggest local pollution sources of PCBs, PCTs, and OCPs. PMID:21616519

  16. The effect of fuel and chlorinated hydrocarbons on a vapor phase carbon adsorption system

    SciTech Connect

    Crawford, W.J.; Cheney, J.L.; Taggart, D.B.

    1995-12-31

    A soil vapor extraction (SVE) system installed at the South Tacoma Well 12A Superfund Site was designed to recover 1,2-dichloroethylene (DCE), trichloroethylene (TCE), tetrachloroethylene (PCE), and 1,1,2,2-tetrachloroethane (1,1,2,2-TCA) from the vadose zone. The basic system consisted of twenty-two extraction wells, three centrifugal blowers, and three carbon adsorbers. The carbon adsorbers were regenerated on site by steam stripping. The mixture of steam and stripped organics was condensed and then decanted to separate the water from the organic phase. The recovered water was air stripped to remove the dissolved organics prior to discharge to the city storm sewer. The recovered organic phase was then shipped off site for thermal destruction. Previous reports described operating difficulties with the decanter, and air strippers. Sampling and analyses were performed which identified the problem as the simultaneous recovery of unexpected fuel hydrocarbons in addition to the solvents. Recovery of fuels resulted in a light phase in the decanter in addition to the water and heavy solvent phases. This required redesign of the decanter to handle the third phase. The effectiveness of desorption of the carbon beds by steam stripping gradually decreased as the remediation progressed into the second year of operation. Samples were collected from the carbon beds to evaluate the effect of the fuel and chlorinated hydrocarbons on the activated carbon. This report describes the results of these analyses. The data indicated that both 1,1,2,2-TCA and fuel hydrocarbons in the C-9 to C-24 range remained in the carbon beds after steam regeneration in sufficient quantities to require replacing the carbon.

  17. Comparison of Reductive Dechlorination of Chlorinated Ethylene in Batch and Continuous-Flow Reactor

    NASA Astrophysics Data System (ADS)

    Park, S.; Jonghwan, L.; Hong, U.; Kim, N.; Ahn, H.; Lee, S.; Kim, Y.

    2010-12-01

    A 1.28 L-Batch reactor and continuous-flow stirred tank reactor (CFSTR) fed with formate and trichloriethene (TCE) were operated for 120 days and 72 days, respectively, to study the effect of formate as electron donor on reductive dechlorination of TCE to cis-1,2-dichloroethylene (c-DCE), vinyl chloride (VC), and ethylene (ETH). In batch reactor, injected 60 μmol TCE was completely degraded in presence of 20% hydrogen gas (H2) in less than 8 days by Evanite culture (300 mg-soluble protein) with ability to completely degrade tetrachloroethene (PCE) and TCE to ETH under anaerobic conditions. To determine the effect of formate as electron donor instead of H2, about 3 or 11 mmol of formate injected into batch-reactor every 15 days was enough to support H2 for dechlorination of c-DCE to VC and ETH. Soluble protein concentration of Evanite culture during the batch test increased from 300 mg to 688 mg for 120 days. In CFSTR test, TCE was fed continuously at 9.9 ppm (75.38 μmol/L) and the influent formate feed concentration increased stepwise from 1.3 mmol/L to 14.3 mmol/L. Injected TCE was accumulated at HRT 18 days for 13 days, but TCE was completed degraded at HRT 36 days without accumulation during left of experiment period, getting H2 from fermentative hydrogen production of injected formate. Although c-DCE was also accumulated for 23 days after CFSTR operation, it reached steady-state without accumulation in presence of excessive formate. However, since c-DCE in CFSTR was not completely dechlorinated, we will determine the transcriptional level of enzyme involved in reductive dechlorination of TCE, c-DCE, and VC in our future work.

  18. Evaluation of exposure to contaminated drinking water and specific birth defects and childhood cancers at Marine Corps Base Camp Lejeune, North Carolina: a case–control study

    PubMed Central

    2013-01-01

    Background Drinking water supplies at Marine Corps Base Camp Lejeune were contaminated with trichloroethylene, tetrachloroethylene, benzene, vinyl chloride and trans-1,2-dichloroethylene during 1968 through 1985. Methods We conducted a case control study to determine if children born during 1968–1985 to mothers with residential exposure to contaminated drinking water at Camp Lejeune during pregnancy were more likely to have childhood hematopoietic cancers, neural tube defects (NTDs), or oral clefts. For cancers, exposures during the first year of life were also evaluated. Cases and controls were identified through a survey of parents residing on base during pregnancy and confirmed by medical records. Controls were randomly sampled from surveyed participants who had a live birth without a major birth defect or childhood cancer. Groundwater contaminant fate and transport and distribution system models provided estimates of monthly levels of drinking water contaminants at mothers’ residences. Magnitude of odds ratios (ORs) was used to assess associations. Confidence intervals (CIs) were used to indicate precision of ORs. We evaluated parental characteristics and pregnancy history to assess potential confounding. Results Confounding was negligible so unadjusted results were presented. For NTDs and average 1st trimester exposures, ORs for any benzene exposure and for trichloroethylene above 5 parts per billion were 4.1 (95% CI: 1.4-12.0) and 2.4 (95% CI: 0.6-9.6), respectively. For trichloroethylene, a monotonic exposure response relationship was observed. For childhood cancers and average 1st trimester exposures, ORs for any tetrachloroethylene exposure and any vinyl chloride exposure were 1.6 (95% CI: 0.5-4.8), and 1.6 (95% CI: 0.5-4.7), respectively. The study found no evidence suggesting any other associations between outcomes and exposures. Conclusion Although CIs were wide, ORs suggested associations between drinking water contaminants and NTDs. ORs suggested

  19. Risk assessment of exposure to volatile organic compounds in groundwater in Taiwan.

    PubMed

    Fan, Chihhao; Wang, Gen-Shuh; Chen, Yen-Chuan; Ko, Chun-Han

    2009-03-15

    The purpose of this study is to assess the risks from exposure to 14 volatile organic compounds (VOCs) in selected groundwater sites in Taiwan. The study employs the multimedia environment pollutant assessment system (MEPAS) model to calculate the specific non-cancer and cancer risks at an exposure level of 1 microg/L of each VOC for a variety of exposure pathways. The results show that the highest specific non-cancer risk is associated with water ingestion of vinyl chloride (VC) and that the highest specific cancer risk is associated with indoor breathing of VC. The three most important exposure pathways for risk assessment for both non-cancer and cancer risks are identified as water ingestion, dermal absorption when showering, and indoor breathing. Excess tetrachloroethylene (PCE), trichloroethylene (TCE), dichloroethylene (DCE), and VC are detected in the groundwater aquifers of one dump site and one factory. However, the study suggests that the pollutants in the contaminated groundwater aquifers do not travel extensively with groundwater flow and that the resulting VOC concentrations are below detectable levels for most of the sampled drinking-water treatment plants. Nevertheless, the non-cancer and cancer risks resulting from use of the contaminated groundwater are found to be hundred times higher than the general risk guidance values. To ensure safe groundwater utilisation, remediation initiatives for soil and groundwater are required. Finally, the study suggests that the current criteria for VOCs in drinking water might not be capable of ensuring public safety when groundwater is used as the primary water supply; more stringent quality criteria for drinking water are proposed for selected VOCs. PMID:19167026

  20. Environmental protection investigations and corrections series: Distribution of VOCs (volatile organic compounds) in round water in the southeast area of LLNL and vicinity

    SciTech Connect

    Dresen, M.D.; Nichols, E.M.

    1986-12-01

    Lawrence Livermore National Laboratory (LLNL) drilled 22 soil borings and 25 monitor wells to investigate the distribution of volatile organic compounds (VOCs) in ground water in the southeast area of LLNL and vicinity. Samples of saturated and unsaturated soil and ground water were collected and analyzed for VOCs. We have used these geologic and chemical data to define the vertical and horizontal distribution of VOCs in ground water. Ground water flow and VOC migration appear to be generally southward in the study area and are integrally related to the subsurface geology. The relatively shallow depth of the low-permeability, low piezometric head, lower member of the Livermore Formation in the study area has induced a significant downward gradient, apparently causing ground water and VOCs to migrate southward in permeable sediments near the contact between the upper and lower members of the Livermore Formation. Trichloroethylene (TCE), tetrachloroethylene (PCE), 1,1-dichloroethylene (1,1-DCE), and carbon tetrachloride (CCl/sub 4/) have been detected in ground water in the study area in concentrations exceeding action levels recommended by the California Department of Health Services (DOHS). TCE is the predominant VOC in the study area. Ground water chemistry and site history data indicate that there are three main sources of VOCs in ground water in the study area and vicinity. A suspected VOC source just south of Building 518 is characterized by TCE with low concentrations of 1,1-DCE, PCE, and CCl/sub 4/. A second VOC source in the Building 612 yard/Building 514 area is characterized by higher concentrations of 1,1-DCE and CCl/sub 4/ relative to TCE. A third source in the Taxi Strip/Old Salvage Yard area north of the study area is characterized by TCE with or without very low concentrations of CCl/sub 4/.

  1. Coupling of zero valent iron and biobarriers for remediation of trichloroethylene in groundwater.

    PubMed

    Teerakun, Mullika; Reungsang, Alissara; Lin, Chien-Jung; Liao, Chih-Hsiang

    2011-01-01

    This study attempted to construct a three series barrier system to treat high concentrations of trichloroethylene (TCE; 500 mg/L) in synthetic groundwater. The system consisted of three reactive barriers using iron fillings as an iron-based barrier in the first column, sugarcane bagasse mixed with anaerobic sludge as an anaerobic barrier in the second column, and a biofilm coated on oxygen carbon inducer releasing material as an aerobic barrier in the third column. In order to evaluate the extent of removal of TCE and its metabolites in the aquifer down gradient of the barrier system, a fourth column filled with sand was applied. Residence time of the system was investigated by a bromide tracer test. The results showed that residence time in the column system of the control set and experimental set were 23.62 and 29.99 days, respectively. The efficiency of the three series barrier system in removing TCE was approximately 84% in which the removal efficiency of TCE by the iron filling barrier, anaerobic barrier and aerobic barrier were 42%, 16% and 25%, respectively, cis-Dichloroethylene (cis-DCE), vinyl chloride (VC), ethylene and chloride ions were observed as metabolites following TCE degradation. The presence of chloride ions in the effluent from the column system indicated the degradation of TCE. However, cis-DCE and VC were not fully degraded by the proposed barrier system which suggested that another remediation technology after the barrier treatment such as air sparging and adsorption by activated carbon should be conducted. PMID:21793396

  2. An association of human congenital cardiac malformations and drinking water contaminants

    SciTech Connect

    Goldberg, S.J.; Lebowitz, M.D.; Graver, E.J.; Hicks, S. )

    1990-07-01

    During an informal study in 1973 it was noted that approximately one third of patients with congenital heart disease lived in a small area in the Tucson Valley. In 1981 groundwater for a nearly identical area was found to be contaminated with trichloroethylene and to a lesser extent with dichloroethylene and chromium. Contamination probably began during the 1950s. Affected wells were closed after discovery of contamination. This sequence of events allowed investigation of the prevalence of congenital heart disease in children whose parents were exposed to the contaminated water area as compared with children whose parents were never exposed to the contaminated water area. The contaminated water area contained 8.8% of the Tucson Valley population and 4.5% of the labor force. Using their case registry, the authors interviewed parents of 707 children with congenital heart disease who, between 1969 and 1987, (1) conceived their child in the Tucson Valley, and (2) spent the month before the first trimester and the first trimester of the case pregnancy in the Tucson Valley. Two random dialing surveys showed that only 10.5% of the Tucson Valley population had ever had work or residence contact, or both, with the contaminated water area, whereas 35% of parents of children with congenital heart disease had had such contact (p less than 0.005). The prevalence of congenital cardiac disease in the Tucson Valley was 0.7% of live births and with syndromes was calculated to be 0.82%. The odds ratio for congenital heart disease for children of parents with contaminated water area contact during the period of active contamination was three times that for those without contact (p less than 0.005) and decreased to near unity for new arrivals in the contaminated water area after well closure.

  3. Characterization of ambient volatile organic compounds and their sources in Beijing, before, during, and after Asia-Pacific Economic Cooperation China 2014

    NASA Astrophysics Data System (ADS)

    Li, J.; Xie, S. D.; Zeng, L. M.; Li, L. Y.; Li, Y. Q.; Wu, R. R.

    2015-07-01

    Ambient volatile organic compounds (VOCs) were measured using an online system, gas chromatography-mass spectrometry/flame ionization detector (GC-MS/FID), in Beijing, China, before, during, and after Asia-Pacific Economic Cooperation (APEC) China 2014, when stringent air quality control measures were implemented. Positive matrix factorization (PMF) was applied to identify the major VOC contributing sources and their temporal variations. The secondary organic aerosols potential (SOAP) approach was used to estimate variations of precursor source contributions to SOA formation. The average VOC mixing ratios during the three periods were 86.17, 48.28, and 72.97 ppbv, respectively. The mixing ratios of total VOC during the control period were reduced by 44 %, and the mixing ratios of acetonitrile, halocarbons, oxygenated VOCs (OVOCs), aromatics, acetylene, alkanes, and alkenes decreased by approximately 65, 62, 54, 53, 37, 36, and 23 %, respectively. The mixing ratios of all measured VOC species decreased during control, and the most affected species were chlorinated VOCs (chloroethane, 1,1-dichloroethylene, chlorobenzene). PMF analysis indicated eight major sources of ambient VOCs, and emissions from target control sources were clearly reduced during the control period. Compared with the values before control, contributions of vehicular exhaust were most reduced, followed by industrial manufacturing and solvent utilization. Reductions of these three sources were responsible for 50, 26, and 16 % of the reductions in ambient VOCs. Contributions of evaporated or liquid gasoline and industrial chemical feedstock were slightly reduced, and contributions of secondary and long-lived species were relatively stable. Due to central heating, emissions from fuel combustion kept on increasing during the whole campaign; because of weak control of liquid petroleum gas (LPG), the highest emissions of LPG occurred in the control period. Vehicle-related sources were the most important

  4. Characterization of ambient volatile organic compounds and their sources in Beijing, before, during, and after Asia-Pacific Economic Cooperation China 2014

    NASA Astrophysics Data System (ADS)

    Li, J.; Xie, S. D.; Zeng, L. M.; Li, L. Y.; Li, Y. Q.; Wu, R. R.

    2015-04-01

    Ambient volatile organic compounds (VOCs) were measured using an online system, gas chromatography-mass spectrometry/flame ionization detector (GC-MS/FID), in Beijing, China, before, during and after Asia-Pacific Economic Cooperation (APEC) China 2014, when stringent air quality control measures were implemented. Positive matrix factorization (PMF) was applied to identify the major VOC contributing sources and their temporal variations. The secondary organic aerosols potential (SOAP) approach was used to estimate variations of precursor source contributions to SOA formation. The average VOC mixing ratios during the three periods were 86.17, 48.28, and 72.97 ppbv, respectively. The mixing ratios of total VOC during the control period were reduced by 44%, and the mixing ratios of acetonitrile, halocarbons, oxygenated VOCs (OVOCs), aromatics, acetylene, alkanes, and alkenes decreased by approximately 65, 62, 54, 53, 37, 36, and 23%, respectively. The mixing ratios of all measured VOC species decreased during control, and the most affected species were chlorinated VOCs (chloroethane, 1,1-dichloroethylene, chlorobenzene). PMF analysis indicated eight major sources of ambient VOCs, and emissions from target control sources were clearly reduced during the control period. Contributions of vehicular exhaust were most reduced (19.65 ppbv, the contributions before the control period minus the values after the control period), followed by industrial manufacturing (10.29 ppbv) and solvent utilization (6.20 ppbv). Contributions of evaporated or liquid gasoline and industrial chemical feedstock were slightly reduced, with values of 2.85 and 0.35 ppbv, respectively. Contributions of secondary and long-lived species were relatively stable. Due to central heating, emissions from fuel combustion kept on increasing during the whole campaign; because of weak control of liquid petroleum gas (LPG), the highest emissions of LPG occurred in the control period. Vehicle-related sources were

  5. Hanford Site groundwater monitoring for Fiscal Year 1997

    SciTech Connect

    Hartman, M.J.; Dresel, P.E.

    1998-02-01

    This report presents the results of groundwater and vadose-zone monitoring for fiscal year (FY) 1997 on the Hanford Site, Washington. Soil-vapor extraction continued in the 200-West Area to remove carbon tetrachloride from the vadose zone. Characterization and monitoring of the vadose zone comprised primarily spectral gamma logging, soil-vapor monitoring, and analysis and characterization of sediments sampled below a vadose-zone monitoring well. Source-term analyses for strontium-90 in 100-N Area vadose-zone sediments were performed using recent groundwater-monitoring data and knowledge of strontium`s ion-exchange properties. Water-level monitoring was performed to evaluate groundwater-flow directions, to track changes in water levels, and to relate such changes to evolving disposal practices. Water levels over most of the Hanford Site continued to decline between June 1996 and June 1997. Water levels near the Columbia River increased during this period because the river stage was unusually high. Groundwater chemistry was monitored to track the extent of contamination, to note trends, and to identify emerging groundwater-quality problems. The most widespread radiological contaminant plumes were tritium and iodine-129. Concentrations of technetium-99, uranium, strontium-90, and carbon-14 also exceeded drinking water standards in smaller plumes. Plutonium and cesium-137 exceeded standards only near the 216-B-5 injection well. Derived concentration guide levels specified in U.S. Department of Energy Order 5400.5 were exceeded for tritium, uranium, strontium-90, and plutonium in small plumes or single wells. Nitrate is the most extensive chemical contaminant. Carbon tetrachloride, chloroform, chromium, cis-1,2-dichloroethylene, fluoride, and trichloroethylene also were present in smaller areas at levels above their maximum contaminant levels. Cyanide concentrations were elevated in one area but were below the maximum contaminant level.

  6. Residues of DDTs and their spatial distribution characteristics in soils from the Yangtze River Delta, China.

    PubMed

    Li, Qingbo; Zhang, Haibo; Luo, Yongming; Song, Jing; Wu, Longhua; Ma, Jianmin

    2008-01-01

    Organochlorine pesticides were used extensively in the Yangtze River Delta, China. However, knowledge about their residual levels and environmental fates in soils of this area is limited. This paper presents the residue isomers and spatial pattern of dichlorodiphenyltrichloroethane (DDT) in soils across 17 main cities in the Yangtze River Delta. Forty-three soil surface (0-15 cm) samples were collected during a field campaign conducted in October 2003 in the Delta. Six DDT isomers (1-[2-chlorophenyl]-1-[4-chlorophenyl]-2,2-dichloroethane [o,p'-DDD], 1-[2-chlorophenyl]-1-[4-chlorophenyl]-2,2-dichloroethylene [o,p-'DDE], 1,1,1-trichloro-2-[p-chlorophenyl]-2-[o-chlorophenyl]ethane [o,p'-DDT], p,p'-dichlorodiphenyldichloroethane [p,p'-DDD], p,p'-dichlorodiphenyldichloroethylene [p,p'-DDE], p,p'-dichlorodiphenyltrichloroethane [p,p'-DDT]) were detected using gas chromatography. The results show that p,p'-DDE was the dominant isomer in the soil samples. The levels of DDT are generally low in soils of this area and are comparable to DDT levels in other cities in China and in soils from developed countries such as the United States and Germany. The isomer ratios of o,p'-DDT to p,p'-DDT and DDT to (DDD + DDE) were employed to identify the source of DDT. The computed ratios implied that the source of DDT might be related to the application of dicofol, an acaricide manufactured from technical DDTs and mainly used on cotton fields to treat mites. PMID:18092878

  7. Chronic toxicity of a mixture of chlorinated alkanes and alkenes in ICR mice.

    PubMed

    Wang, Fun-In; Kuo, Min-Liang; Shun, Chia-Tung; Ma, Yee-Chung; Wang, Jung-Der; Ueng, Tzuu-Huei

    2002-02-01

    The aim of this study was to determine the chronic toxicity of a mixture of chlorinated alkanes and alkenes (CA) consisting of chloroform, 1,1-dichloroethane, 1,1-dichloroethylene, 1,1,1-trichloroethane, trichloroethylene, and tetrachloroethylene. These chlorinated organic solvents were present in the underground water near an electronic appliances manufactory in Taoyuan, Taiwan. Male and female weanling ICR mice were treated with low-, medium-, and high-dose CA mixtures in drinking water for 16 and 18 mo, respectively. A significant number of male mice treated with the high-dose CA mixture developed tail alopecia and deformation, which was not prominent in CA-treated female mice. Medium- and high-dose CA mixtures induced marginal increases of liver and lung weights, blood urea nitrogen, and serum creatinine levels in male mice. In female mice, the high-dose CA mixture increased liver, kidney, and uterus and ovary total weights, without affecting serum biochemistry parameters. CA mixtures had no effects on the total glutathione content or the level of glutathione S-transferase activity in the livers and kid- neys of male and female mice. Treatments with CA mixtures produced a trend of increasing frequency of hepatocelluar neoplasms in male mice, compared to male and female controls and CA-treated female mice. The high-dose CA mixture induced a significantly higher incidence of mammary adenocarcinoma in female mice. The calculated odds ratios of mammary adenocarcinoma in female mice induced by low-, medium-, and high-dose CA mixtures were 1.14, 1.37, and 3.53 times that of the controls, respectively. The low-dose CA mixture induced a higher incidence of cysts and inflammation in and around the ovaries. This study has demonstrated that the CA mixture is a potential carcinogen to male and female mice. These animal toxicology data may be important in assessing the health effects of individuals exposed to the CA mixture. PMID:11911491

  8. Annually-layered lake sediments reveal strongly increased release of persistent chemicals due to accelerated glacier melting

    NASA Astrophysics Data System (ADS)

    Anselmetti, Flavio S.; Blüthgen, Nancy; Bogdal, Christian; Schmid, Peter

    2010-05-01

    Melting glaciers may represent a secondary source of chemical pollutants that have previously been incorporated and stored in the ice. Of particular concern are persistent organic pollutants (POPs), such as the insecticide dichlorodiphenyl trichloroethane (DDT) and industrial chemicals like polychlorinated biphenyls (PCBs), which are hazardous environmental contaminants due to their persistent, bioaccumulative and toxic properties. They were introduced in the 1930s and eventually banned in the 1970s. After release into the environment these chemicals were atmospherically transported to even remote areas such as the Alps and were deposited and stored in glaciers. Ongoing drastic glacier melting due to global warming, which is expected to further accelerate, implies the significance of studying the fate of these 'legacy pollutants'. Proglacial lake sediments provide well-dated and high-resolution archives to reconstruct timing and quantities of such a potentially hazardous remobilization. The goal of this study is to reconstruct the historical inputs of POPs into remote alpine lakes and to investigate the accelerated release of POPs from melting glaciers. Due to their lipophilic character, these chemicals exhibit a high tendency to adsorb to particles whereas concentrations in water are expected to be low. Therefore, quantitative determination in annually-layered lake sediment provides an excellent way to investigate the temporal trend of inputs into lakes that act as particle sinks. For this purpose, sediment cores were sampled from proglacial lakes in the Bernese Alps (Switzerland), which are exclusively fed by glacial melt waters. For comparison, cores were also taken from nearby high-alpine lakes located in non-glaciated catchments, which only should record the initial atmospheric fall-out. Sediment layers were dated by annual varve counting and radionuclide measurements; they cover the time period from the mid 20th century to today. The measured time series of

  9. Comparison of migration from polyethersulphone and polycarbonate baby bottles.

    PubMed

    Simoneau, C; Valzacchi, S; Morkunas, V; Van den Eede, L

    2011-12-01

    This work presents two analytical methods developed for measuring three components of polyethersulphone (PES) and applying them to the migration testing of 30 baby bottles made of PES. The study also provides migration results under the same conditions for bisphenol A (BPA) from 40 polycarbonate baby bottles using a well-established method adapted to low concentrations. For PES bottles, migration of diphenyl sulphone (DPS), 4,4'-dichlorodiphenyl sulphone (DCPS) and 4,4'-dihydroxydiphenyl sulphone (DHPS; also known as bisphenol S) was carried out using two different analytical methods with detection limits of 0.1-0.3 µg/kg, and, therefore, much below their respective European Commission Directive 2002/72/EC legislative migration limits of 50-3000 µg/kg, respectively. In parallel, 40 bottles made of polycarbonate were analysed for the migration of BPA using a method validated at EU level and modified to give a lower detection limit of 0.1 µg/kg. Migration tests were conducted into the simulant for milk 50% EtOH (as per Commission Regulation No. 321/2011 of 1 April 2011) according to the test conditions from the guidelines on test conditions for articles in contact with foodstuffs (with a focus on kitchenware) prepared by the EU Reference Laboratory and its network of National Reference Laboratories. None of the 30 bottles made of PES released any detectable amounts of DCPS or DHPS and only two bottles released a very low amount of DPS of ~1 µg/kg in the milk food simulant compared to a regulatory limit of 3000 µg/kg. For PC bottles, 32 bottles of 40 (80%) did not release BPA above the LOD of 0.1 µg/kg (in any of the three migration tests performed on each bottle). The other 20% of bottles exhibited only very minor migration, where the highest level in the first migration test was 1.83 µg/kg and most bottles did not release detectable BPA in the second and third test. Only one bottle, with a migration level of 1.08 µg/kg, in the first test still showed a

  10. Post-remediation biomonitoring of pesticides and other contaminants in marine waters and sediment near the United Heckathorn Superfund Site, Richmond, California

    SciTech Connect

    LD Antrim; NP Kohn

    2000-05-26

    Marine sediment remediation at the United Heckathorn Superfund Site was completed in April 1997. Water and mussel tissues were sampled in February 1999 from four stations near Lauritzen Canal in Richmond, California, for Year 2 of post-remediation monitoring of marine areas near the United Heckathorn Site. Dieldrin and dichlorodiphenyl trichloroethane (DDT) were analyzed in water samples, tissue samples from resident mussels, and tissue samples from transplanted mussels deployed for 4 months. Concentrations of dieldrin and total DDT in water and total DDT in tissue were compared with Year 1 of post-remediation monitoring, and with preremediation data from the California State Mussel Watch program (tissues) and the Ecological Risk Assessment for the United Heckathorn Superfund Site (tissues and water). Mussel tissues were also analyzed for polychlorinated biphenyls (PCB), which were detected in sediment samples. Chlorinated pesticide concentrations in water samples were similar to preremediation levels and did not meet remediation goals. Mean dieidrin concentrations in water ranged from 0.62 rig/L to 12.5 ng/L and were higher than the remediation goal (0.14 ng/L) at all stations. Mean total DDT concentrations in water ranged from 14.4 ng/L to 62.3 ng/L and exceeded the remediation goal (0.59 ng/L) at all stations. The highest concentrations of both pesticides were found at the Lauritzen Canal/End station. Despite exceedence of the remediation goals, chlorinated pesticide concentrations in Lauritzen Canal water samples were notably lower in 1999 than in 1998. Tissue samples from biomonitoring organisms (mussels) provide an indication of the longer-term integrated exposure to contaminants in the water column, which overcomes the limitations of grab samples of water. Biomonitoring results indicated that the bioavailability of chlorinated pesticides has been reduced from preremediation levels both in the dredged area and throughout Richmond Harbor. Total DDT and

  11. Ground-water quality in the West Salt River Valley, Arizona, 1996-98: relations to hydrogeology, water use, and land use

    USGS Publications Warehouse

    Edmonds, Robert J.; Gellenbeck, Dorinda J.

    2002-01-01

    February 1998. Analyses of all samples collected from the monitoring wells indicated low concentrations of pesticides and volatile organic compounds. The most frequently detected pesticides were deethylatrazine and atrazine. Trichloromethane (chloroform) and tetrachloroethene (PCE) were the most frequently detected volatile organic compounds in the monitoring wells. Two compounds [dieldrin and 1,1-dichloro-2,2-bis(p-dichlorodiphenyl)ethylene (DDE)], decomposition products of two banned pesticides, aldrin and dichlorodiphenylethylene (DDT), were detected at low concentrations in samples analyzed for the agricultural land-use study. In the West Salt River Valley, a high concentration of the heavier oxygen isotope?oxygen-18?in ground water generally indicates effects of evaporation on recharge water from irrigation. Wells in undeveloped areas and wells that have openings beneath a confining bed generally yield ground water that is free of the effects of irrigation seepage. Samples from these wells did not contain detectable concentrations of pesticides. The median concentrations of nitrate (as nitrogen) and dissolved solids in samples from wells in undeveloped areas were 1.7 milligrams per liter and 257 milligrams per liter, respectively. The median concentrations of nitrate (as nitrogen) and dissolved solids in samples from wells that yield water from below confining beds were 2.0 and 747 milligrams per liter, respectively.

  12. Persistence, variance and toxic levels of organochlorine pesticides in fluvial sediments and the role of black carbon in their retention.

    PubMed

    Parween, Musarrat; Ramanathan, Al; Khillare, P S; Raju, N J

    2014-05-01

    The present study assesses the persistence and variation of organochlorine pesticides (OCPs) and their regulation by total organic carbon (TOC) and black carbon (BC) in freshwater sediment. Sediment samples from the Yamuna River, a major tributary of the Ganges (one of the most populated and intensively used rivers in Asia), had high levels of Σ20OCPs (21.41 to 139.95 ng g(-1)). β-Hexachlorocyclohexane (β-HCH) was the most predominant component. ΣHCH and Σdichloro-diphenyl-trichloroethane (DDT) constituted ~86% of Σ20OCPs. Isomer ratios indicated fresh usage of lindane, DDT and technical-grade HCH. Toxicological comparison with freshwater sediment quality guidelines showed γ-HCH and DDT at high levels of concern. β-HCH, α-HCH, endrin, heptachlor epoxide, dichloro-diphenyl-dichloroethane (DDD), dichloro-diphenyl-dichloroethylene and chlordane were above some of the guideline levels. TOC and BC had mean concentrations of 1.37 ± 0.51% and 0.46 ± 0.23 mg g(-1), respectively. BC constituted 1.25 to 10.56% of TOC. We observed low to moderate correlations of BC with isomers of HCH, p,p'-DDT and methoxychlor while of TOC with Σ20OCPs, γ-HCH, endosulfan sulfate and methoxychlor. Principal component analysis enabled correlating and clustering of various OCPs, BC and TOC. OCP distribution was related with pH, electrical conductivity, soil moisture and finer fractions of sediment. OCPs with similarity in properties that determine their interactions with carbonaceous components of sediment clustered together. A number of factors may, thus, be involved in the regulation of interactive forces between BC and OCPs. BC in this study may be more important than TOC in the retention of some OCPs into fluvial sediments, thereby reducing their bioavailability. The finding is probably the first of its kind to report and emphasises the role of BC in the persistence of OCPs in fluvial sediments. PMID:24488553

  13. Reconnaissance investigation of volatile and semivolatile organic compounds in the Memphis Aquifer at Alamo, Crockett County, Tennessee

    USGS Publications Warehouse

    Hutson, Susan S.; Haugh, Connor J.

    1992-01-01

    Samples of ground water and soil gas were analyzed to study the occurrence of volatile and semivolatile organic compounds in the Memphis aquifer at Alamo in western Tennessee in 1989. At Alamo, the aquifer is locally unconfined. Four wells screened in the Memphis aquifer provided Alamo with 0.3 million gallons of water per day. Trichloroethylene (TCE), dichloroethylene, trichloroethane, and tetrachloroethylene were detected in water samples from two of the wells. In September 1989, the TCE concentration in a sample from well 1 was 45 micrograms per liter (mg/L); Tennessee?s maximum contaminant level for TCE in drinking water is 5 mg/L Concentrations of TCE in water from this well ranged from 40 to 113 mg/L during I988 and 1989. TCE concentration in water collected from well 2 in September 1989 was 0.7 mg/L During I988 and 1989, TCE concentrations in this well ranged from less than 0.5 to 5.1 mg/L None of the semivolatile organic compounds on the U.S. Environmental Protection Agency?s priority-pollutant list were detected in water from well 1. Soil gas was sampled at a depth of 3.5 feet below land surface in areas of suspected ground-water contamination. Analyses by gas chromatography indicated the presence of TCE in soils about 230 feet east of well 1 in the area of a former industrial site where solvents were handled. TCE concentrations in the soil gas of this area ranged from 0.2 to 30 mg/L TCE was not detected in soil gas near any of the wells. Depth to water at the wells ranged from 39 to 49 feet. The regional direction of ground-water flow is to the west-southwest, which would cause contaminants dissolved in ground water below the former industrial-site area to be transported toward the public-supply wells. Probable reasons contributing to the lack of TCE detection in soil gas at wells 1 and 2 are the relatively low concentrations of TCE in ground water at the wells and the vertical distance between sampling points and the water table.

  14. Streambed-material characteristics and surface-water quality, Green Pond Brook and tributaries, Picatinny Arsenal, New Jersey, 1983-90

    USGS Publications Warehouse

    Storck, D.A.; Lacombe, Pierre

    1996-01-01

    This report presents the results of a study designed to determine whether Green Pond Brook and its tributaries contain contaminated streambed sediments and to characterize the quaity of water in the brook. Results of previous investigations at Picatinny Arsenal, Morris County, New Jersey, indicate that significant contamination of ground water, surface water, and soil is present at the arsenal. Forty-five streambed-material samples were collected for analysis to determine whether contaminants have migrated to the brook from the surrounding area. Samples were analyzed for trace elements, base/neutral- and acid-etractable compounds, insecticides, and other constituents. Results of an electromagnetic-conductivity and natural-gamma-ray survey were used to describe the distribution of particle sizes in streambed and substreambed sediments. Historical results of analyses of streambed-material and surface-water samples also are presented. Samples of streambed material from three areas in Green Pond Brook and its tributaries contained organic and (or) inorganic constituents in concentrations greater than those typically found at the arsenal. These areas are Green Pond Brook, from the area near the outflow of Picatinny Lake downstream to Farley Avenue; Bear Swamp Brook, from the area near building 241 downstream to the confluence with Green Pond Brook; and Green Pond Brook, from the open burning area downstream to the dam near building 1178. Contaminants identified include trace elements, polynuclear aromatic hydrocarbons, polychlorinated biphenyls, and organochlorine insecticides. Surface water in Green Pond Brook contained several volatile organic compounds, including trichloroethylene, tetrachloroethylene, and 1,2-dichloroethylene, at maximum concen- trations of 3.8, 4.6, and 11 micrograms per liter, respectively. Volatilization is expected to remove volatile organic compounds in the steep, fast- flowing reaches of the brook. No organic or inorganic constituents were

  15. Trichloroethylene effects on gene expression during cardiac development

    SciTech Connect

    Collier, John Michael; Selmin, Ornella; Johnson, Paula D.; Runyan, Raymond B.

    2003-05-09

    Background: Halogenated hydrocarbon exposure is associated with changes in gene expression in adult and embryonic tissue. The present study was undertaken to identify differentially expressed mRNA transcripts in embryonic hearts from Sprague-Dawley rats exposed to trichloroethylene (TCE) or potential bio-transformation products of TCE, Dichloroethylene (DCE) and Trichloroacetic acid (TCAA). Methods: cDNA subtractive hybridization was used to selectively amplify expressed mRNA in either control or day 11 embryonic rat hearts exposed to one of these halogenated hydrocarbons from day 0 to 11. The doses used were 1100 and 110 ppm (8300 and 830 mu M) TCE, 110 and 11 ppm (1100 and 110 mu M) DCE, 27.3 and 2.75 mg/ml (100 and 10 mM) TCAA. Control animals were given distilled drinking water throughout the period of experiments. Results: Sequencing of over 100 clones derived from halogenated hydrocarbon exposed groups=resulted in identification of numerous differentially regulate gene sequences. Up-regulated transcripts identified include genes associated with stress response (Hsp 70) and homeostasis (several ribosomal proteins). Down-regulated transcripts include extracellular matrix components (GPI-p137 and vimentin) and Ca2 + responsive proteins (Serca-2 Ca2+-ATPase and beta-catenin). Two possible markers for fetal TCE exposure were identified: Serca-2 and GPI-p137, a GPI-linked protein of unknown function. Both markers show a dose-related decrease in mRNA transcript levels associated with fetal exposure to TCE. Differential regulation of expression of both markers by TCE was confirmed by dot blot analysis and semi-quantitative RT-PCR. Levels of exposure between 100 and 250 ppb (0.76 and 1.9 mu M) TCE are sufficient to decrease expression of both the Ca2+-AT Pase and GPI-p137. Conclusion: Sequences down-regulated with TCE exposure appear to be those associated with cellular=housekeeping, cell adhesion and developmental processes, while TCE=exposure up-regulates expression

  16. Mass of chlorinated volatile organic compounds removed by Pump-and-Treat, Naval Air Warfare Center, West Trenton, New Jersey, 1996-2010

    USGS Publications Warehouse

    Lacombe, Pierre J.

    2011-01-01

    Pump and Treat (P&T) remediation is the primary technique used to contain and remove trichloroethylene (TCE) and its degradation products cis 1-2,dichloroethylene (cDCE) and vinyl chloride (VC) from groundwater at the Naval Air Warfare Center (NAWC), West Trenton, NJ. Three methods were used to determine the masses of TCE, cDCE, and VC removed from groundwater by the P&T system since it became fully operational in 1996. Method 1, is based on the flow volume and concentrations of TCE, cDCE, and VC in groundwater that entered the P&T building as influent. Method 2 is based on withdrawal volume from each active recovery well and the concentrations of TCE, cDCE, and VC in the water samples from each well. Method 3 compares the maximum monthly amount of TCE, cDCE, and VC from Method 1 and Method 2. The greater of the two values is selected to represent the masses of TCE, cDCE and VC removed from groundwater each month. Previously published P&T monthly reports used Method 1 to determine the mass of TCE, cDCE, and VC removed. The reports state that 8,666 pounds (lbs) of TCE, 13,689 lbs of cDCE, and 2,455 lbs of VC were removed by the P&T system during 1996-2010. By using Method 2, the mass removed was determined to be 8,985 lbs of TCE, 17,801 lbs of cDCE, and 3,056 lbs of VC removed, and Method 3, resulted in 10,602 lbs of TCE, 21,029 lbs of cDCE, and 3,496 lbs of VC removed. To determine the mass of original TCE removed from groundwater, the individual masses of TCE, cDCE, and VC (determined using Methods 1, 2, and 3) were converted to numbers of moles, summed, and converted to pounds of original TCE. By using the molar conversion the mass of original TCE removed from groundwater by Methods 1, 2, and 3 was 32,381 lbs, 39,535 lbs, and 46,452 lbs, respectively, during 1996-2010. P&T monthly reports state that 24,805 lbs of summed TCE, cDCE, and VC were removed from groundwater. The simple summing method underestimates the mass of original TCE removed by the P&T system.

  17. Competing TCE and cis-DCE degradation kinetics by zero-valent iron-experimental results and numerical simulation.

    PubMed

    Schäfer, Dirk; Köber, Ralf; Dahmke, Andreas

    2003-09-01

    The successful dechlorination of mixtures of chlorinated hydrocarbons with zero-valent metals requires information concerning the kinetics of simultaneous degradation of different contaminants. This includes intraspecies competitive effects (loading of the reactive iron surface by a single contaminant) as well as interspecies competition of several contaminants for the reactive sites available. In columns packed with zero-valent iron, the degradation behaviour of trichloroethylene (TCE), cis-dichloroethylene (DCE) and mixtures of both was measured in order to investigate interspecies competition. Although a decreasing rate of dechlorination is to be expected, when several degradable substances compete for the reactive sites on the iron surface, TCE degradation is nearly unaffected by the presence of cis-DCE. In contrast, cis-DCE degradation rates decrease significantly when TCE is added. A new modelling approach is developed in order to identify and quantify the observed competitive effects. The numerical model TBC (Transport, Biochemistry and Chemistry, Schäfer et al., 1998a) is used to describe adsorption, desorption and dechlorination in a mechanistic way. Adsorption and degradation of a contaminant based on a limited number of reactive sites leads to a combined zero- and first-order degradation kinetics for high and low concentrations, respectively. The adsorption of several contaminants with different sorption parameters to a limited reactive surface causes interspecies competition. The reaction scheme and the parameters required are successfully transferred from Arnold and Roberts (2000b) to the model TBC. The degradation behaviour of the mixed contamination observed in the column experiments can be related to the adsorption properties of TCE and cis-DCE. By predicting the degradation of the single substances TCE and cis-DCE as well as mixtures of both, the calibrated model is used to investigate the effects of interspecies competition on the design of

  18. Competing TCE and cis-DCE degradation kinetics by zero-valent iron—experimental results and numerical simulation

    NASA Astrophysics Data System (ADS)

    Schäfer, Dirk; Köber, Ralf; Dahmke, Andreas

    2003-09-01

    The successful dechlorination of mixtures of chlorinated hydrocarbons with zero-valent metals requires information concerning the kinetics of simultaneous degradation of different contaminants. This includes intraspecies competitive effects (loading of the reactive iron surface by a single contaminant) as well as interspecies competition of several contaminants for the reactive sites available. In columns packed with zero-valent iron, the degradation behaviour of trichloroethylene (TCE), cis-dichloroethylene (DCE) and mixtures of both was measured in order to investigate interspecies competition. Although a decreasing rate of dechlorination is to be expected, when several degradable substances compete for the reactive sites on the iron surface, TCE degradation is nearly unaffected by the presence of cis-DCE. In contrast, cis-DCE degradation rates decrease significantly when TCE is added. A new modelling approach is developed in order to identify and quantify the observed competitive effects. The numerical model TBC (Transport, Biochemistry and Chemistry, Schäfer et al., 1998a) is used to describe adsorption, desorption and dechlorination in a mechanistic way. Adsorption and degradation of a contaminant based on a limited number of reactive sites leads to a combined zero- and first-order degradation kinetics for high and low concentrations, respectively. The adsorption of several contaminants with different sorption parameters to a limited reactive surface causes interspecies competition. The reaction scheme and the parameters required are successfully transferred from Arnold and Roberts (2000b) to the model TBC. The degradation behaviour of the mixed contamination observed in the column experiments can be related to the adsorption properties of TCE and cis-DCE. By predicting the degradation of the single substances TCE and cis-DCE as well as mixtures of both, the calibrated model is used to investigate the effects of interspecies competition on the design of

  19. Baseline risk assessment for groundwater operable units at the Chemical Plant Area and the Ordnance Works Area, Weldon Spring, Missouri

    SciTech Connect

    1999-07-14

    .g., radium and thorium) were measured at back-ground levels and were eliminated from further consideration. Chemical contaminants identified in wells at the chemical plant area and ordnance works area include nitroaromatic compounds, metals, and inorganic anions. Trichloroethylene (TCE) and 1,2-dichloroethylene (1,2 -DCE) have been detected recently in a few wells near the raffinate pits at the chemical plant.

  20. Probabilistic Human Health Risk Assessment of Chemical Mixtures: Hydro-Toxicological Interactions and Controlling Factors

    NASA Astrophysics Data System (ADS)

    Henri, C.; Fernandez-Garcia, D.; de Barros, F.

    2014-12-01

    Improper disposals of hazardous wastes in most industrial countries give rise to severe groundwater contamination problems that can lead to adverse health effects in humans. Therefore risk assessment methods play an important role in population protection by (1) quantifying the impact on human health of an aquifer contamination and (2) aiding the decision making process of to better manage our groundwater resources. Many reactive components such as chlorinated solvent or nitrate potentially experience attenuation processes under common geochemical conditions. Based on this, monitored natural attenuation has become nowadays an attractive remediation solution. However, in some cases, intermediate degradation products can constitute noxious chemical compounds before reaching a harmless chemical form. In these cases, the joint effect of advection-dispersion transport and the species-dependent kinetic reactions and toxicity will dictate the relative importance of the degradation byproducts to the total risk. This renders the interpretation of risk a non-trivial task. In this presentation, we quantify, through a probabilistic framework, the human health risk posed by a chemical mixture in a heterogeneous aquifer. This work focuses on a Perchloroethylene contamination problem followed by the first-order production/biodegradation of its daughter species Trichloroethylene, Dichloroethylene and Vinyl Chlorine that is known to be highly toxic. Uncertainty on the hydraulic conductivity field is considered through a Monte Carlo scheme. A comparative description of human health risk metrics as a function of aquifer heterogeneity and contaminant injection mode is provided by means of a spatial characterization of the lower-order statistical moments and empirical probability density functions of both individual and total risks. Interestingly, we show that the human health risk of a chemical mixture is mainly controlled by a modified Damköhler number that express the joint effect

  1. Assessment of ground-water contamination at Wurtsmith Air Force Base, Michigan, 1982-85

    USGS Publications Warehouse

    Cummings, T.R.; Twenter, F.R.

    1986-01-01

    Study of ground-water contamination at Wurtsmith Air Force Base, Michigan, defined the movement and distribution of volatile organic compounds in the glacial sand and gravel aquifer at known sites of contamination, and has defined new plumes at two other sites. The Arrow Street purge system, installed in 1982 to remove contaminants from the Building 43 plume, has lowered concentrations of trichloroethylene (TCE) in groundwater in the central part of the most contaminated area from a range of 1,000 to 2,000 microg/L to about 200 microg/L. TCE is not escaping off-Base from this area. In the southern part of the Base a plume containing principally TCE and dichloroethylene (DCE) has been delineated along Mission Drive. Maximum concentrations observed were 3,290 microg/L of TCE and 1,480 microg/L of DCE. Hydrologically suitable sites for purge wells were identified in the southern part of the plume using a new ground-water flow model of the Base. A benzene plume near the bulk-fuel storage area has shifted to a more northerly direction under influence of the Arrow Street purge system. Sites initially identified for purging the benzene plume have been repositioned because of the change in contaminant movement. JP-4 fuel was found to be accumulating in wells near the bulk-fuel storage area, largely in response to seasonal fluctuations in the water-table. It is thought to originate from a spill that occurred several years ago. In general, concentrations found in water do not differ greatly from those observed in 1981. Since 1981, concentrations of TCE have decreased significantly in the Alert Apron plume. Near the origin of the plume, the concentration of TCE has decreased from 1,000 microg/L in 1980 to 50 microg/L in 1984. Water from Van Etten Lake near the termination of the plume had only a trace of TCE at one site. Benzene detected in water from well AF2 seems to originate near the former site of buried fuel tanks west of the operational apron. During periods of normal

  2. Interplay between subsurface structural heterogeneity and multi-species reactive transport in human health risk predictions

    NASA Astrophysics Data System (ADS)

    Henri, C.; Fernandez-Garcia, D.; de Barros, F.

    2013-12-01

    The increasing presence of toxic chemicals released in the subsurface has led to a rapid growth of social concerns and to the need to develop and employ models that can predict the impact of groundwater contamination in human health under uncertainty. Monitored natural attenuation is a common remediation action in many contamination cases and represents an attractive decontamination method. However, natural attenuation can lead to the production of subspecies of distinct toxicity that may pose challenges in pollution management strategies. The actual threat that these contaminants pose to human health and ecosystems greatly depends on the interplay between the complexity of the geological system and the toxicity of the pollutants and their byproducts. In this work, we examine the interplay between multispecies reactive transport and the heterogeneous structure of the contaminated aquifer on human health risk predictions. The structure and organization of hydraulic properties of the aquifer can lead to preferential flow channels and fast contamination pathways. Early travel times, associated to channeling effects, are intuitively perceived as an indicator for high risk. However, in the case of multi-species systems, early travel times may also lead a limited production of daughter species that may contain higher toxicity as in the case of chlorinated compounds. In this work, we model a Perchloroethylene (PCE) contamination problem followed by the sequential first-order production/biodegradation of its daughter species Trichloroethylene (TCE), Dichloroethylene (DCE) and Vinyl Chlorine (VC). For this specific case, VC is known to be a highly toxic contaminant. By performing numerical experiments, we evaluate transport for two distinct three-dimensional aquifer structures. First, a multi-Gaussian hydraulic conductivity field and secondly, a geostatistically equivalent connected field. These two heterogeneity structures will provide two distinct ranges of mean travel

  3. Assessing in situ mineralization of recalcitrant organic compounds in vadose zone sediments using delta13C and 14C measurements.

    PubMed

    Kirtland, Brian C; Aelion, C Marjorie; Stone, Peter A

    2005-01-01

    Few techniques exist to measure the biodegradation of recalcitrant organic compounds such as chlorinated hydrocarbons (CHC) in situ, yet predictions of biodegradation rates are needed for assessing monitored natural attenuation. Traditional techniques measuring O2, CO2, or chemical concentrations (in situ respiration, metabolite and soil air monitoring) may not be sufficiently sensitive to estimate biodegradation rates for these compounds. This study combined isotopic measurements (14C and delta13C of CO2 and delta13C of CHCs) in conjunction with traditional methods to assess in situ biodegradation of perchloroethylene (PCE) and its metabolites in PCE-contaminated vadose zone sediments. CHC, ethene, ethane, methane, O2, and CO2 concentrations were measured over 56 days using gas chromatography (GC). delta13C of PCE, trichloroethylene (TCE) and cis-1,2-dichloroethylene (DCE), delta13C and 14C of vadose zone CO2 and sediment organic matter, and delta13C, 14C, and deltaD of methane were measured using a GC-isotope ratio mass spectrometer or accelerator mass spectrometer. PCE metabolites accounted for 0.2% to 18% of CHC concentration suggesting limited reductive dechlorination. Metabolites TCE and DCE were significantly enriched in (13)C with respect to PCE indicating metabolite biodegradation. Average delta13C-CO2 in source area wells (-23.5 per thousand) was significantly lower compared to background wells (-18.4 per thousand) indicating CHC mineralization. Calculated CHC mineralization rates were 0.003 to 0.01 mg DCE/kg soil/day based on lower 14C values of CO2 in the contaminated wells (63% to 107% modern carbon (pMC)) relative to the control well (117 pMC). Approximately 74% of the methane was calculated to be derived from in situ CHC biodegradation based on the 14C measurement of methane (29 pMC). 14C-CO2 analyses was a sensitive measurement for quantifying in situ recalcitrant organic compound mineralization in vadose zone sediments for which limited

  4. Mixtures of four organochlorines enhance human breast cancer cell proliferation.

    PubMed Central

    Payne, J; Scholze, M; Kortenkamp, A

    2001-01-01

    In view of the large differences between the concentrations of estrogenic chemicals needed to elicit effects in in vitro assays and their levels in human tissues, it is hard to explain possible health risks in terms of exposure to individual compounds. Human populations, however, are exposed to mixtures of estrogenic and estrogen-like agents and it is necessary to consider the impact of combined effects. We assessed the combined effects of 1-(o-chlorophenyl)-1-(p-chlorophenyl)-2,2,2-trichloroethane (o,p'-DDT), 2,2-bis(p-chlorophenyl)-1,1-dichloroethylene (p,p'-DDE), beta-hexachlorocyclohexane (beta-HCH), and 1,1-bis(p-chlorophenyl)-2,2,2-trichloroethane (p,p'-DDT) on the induction of cell proliferation in MCF-7 cells. All four compounds are persistent organochlorines that can be found in human tissues. We performed extensive concentration-response analyses with the single agents to predict the effects of two mixtures of all four compounds with different mixture ratios. We calculated the predictions by using the pharmacologically well-founded models of concentration addition and independent action and then tested them experimentally. o,p'-DDT, p,p'-DDE, beta-HCH, and p,p'-DDT acted together to produce proliferative effects in MCF-7 cells. The combined effect of the four agents could be predicted on the basis of data about single agent concentration-response relationships. Regression analysis demonstrated that there were combination effects even when each mixture component was present at levels at or below its individual no-observed-effect-concentration. We assessed combination effects in two ways: First, evaluations in relation to the proliferative responses induced by single mixture components revealed that the combination effects were stronger than the effects of the most potent constituent. Thus, according to this method of evaluation, the combined effects may be termed synergistic. Second, comparisons with the expected effects, as predicted by concentration

  5. Assessing the Feasibility of In-Situ Aerobic Cometabolism of Chlorinated Solvents by a Single-Well Push-Pull and Natural Gradient Drift Tests in McClellan AFB, CA

    NASA Astrophysics Data System (ADS)

    Kim, Y.; Istok, J. D.; Semprini, L.

    2001-12-01

    A single-well push-pull test has been developed to evaluate in-situ aerobic cometabolic treatment of chlorinated aliphatic hydrocarbons (CAHs), such as trichloroethylene (TCE) and cis-1,2-dichloroethylene (c-DCE). A series of single-well natural gradient drift and push-pull tests were conducted in two monitoring wells at the McClellan Air Force Base, CA, where aquifer is contaminated mainly with c-DCE and TCE. Transport characteristics of dissolved solutes [bromide (tracer), propane (growth substrate), ethylene, propylene (nontoxic surrogates to probe for CAH transformation activity), DO and nitrate (nutrient)] were evaluated in push-pull transport tests by injecting 200-L of groundwater containing the solutes into the aquifer (Push), providing a rest period of 18 hours (Reaction), and then extracting 400-L of the test solution/groundwater mixtures (Pull). Mass balances showed over 95% of the injected bromide was recovered, and the recoveries of the other solutes were comparable with bromide. The dispersion of all the solutes was similar indicating sorption or other partitioning processes were minimal. These results indicate that bromide could be used as a conservative tracer for biological activity tests and that little loss of the dissolved gaseous substrates occurred prior to biostimulation of the aquifer. A series of biostimulation tests were performed by injecting 500 L-groundwater containing propane (6 mg/L), DO (25 mg/L), nitrate (9 mg/L as N) and bromide (100 mg/L) into the aquifer. Temporal groundwater samples were obtained from the injection well under natural gradient drift conditions. With repeating biostimulation tests the rates of both propane and DO utilization were increased significantly. The results demonstrated that the progress of biostimulation could be assessed by injecting and monitoring under natural gradient drift conditions. Successive push-pull activity tests were performed after biostimulation was achieved using the same procedures as

  6. Analysis of nitrate and volatile organic compound data for ground water in the Great Salt Lake Basins, Utah, Idaho, and Wyoming, 1980-98, National Water-Quality Assessment Program

    USGS Publications Warehouse

    Thiros, Susan A.

    2000-01-01

    sampled ground water. Overall, water sampled from wells in rangeland areas had a lowermedianmeasured nitrate concentration (0.76 milligrams per liter) than water from areas with an agricultural or urban/residential land use (1.41 and 1.20 milligrams per liter, respectively). In the NationalWater Information System data set, the median measured nitrate concentration in water from urban/residential areas varied from 1.00 milligrams per liter for wells greater than 150 feet deep to 1.84 milligrams per liter for wells less than or equal to 150 feet deep. The Public DrinkingWater Systems and the National Water Information System data sets contained analyses for most of the State and Federally regulated volatile organic compounds in water from about 368 and 74 wells, respectively. Fifteen different volatile organic compounds were detected at least once in ground water sampled from the Great Salt Lake Basins study unit. Water from 21 wells contained at least 1 volatile organiccompound at detectable concentrations. About 68 percent of the volatile organic compounds detected were in water sampled from wells in Salt Lake County, Utah. Tetrachloroethylene was the most commonly detected volatile organic compound in ground water sampled from the study unit, present in 8 out of 442 samples. Maximum contaminant levels for tetrachloroethylene and 1,1-dichloroethylene as established by the U.S. Environmental Protection Agency were exceeded in water from one well each.

  7. Field assessment of carboxymethyl cellulose stabilized iron nanoparticles for in situ destruction of chlorinated solvents in source zones.

    PubMed

    He, Feng; Zhao, Dongye; Paul, Chris

    2010-04-01

    reduction after two weeks. After 596 days from the first injection, the total chlorinated ethenes concentration decreased by about 40% and 61% in MW-1 and MW-2, respectively. No significant long-term reduction of PCB 1242 was observed in MW-1, but a reduction of 87% was evident in MW-2. During the 596 days of testing, the total concentrations of cis-DCE (dichloroethylene) and VC (vinyl chloride) decreased by 20% and 38% in MW-1 and MW-2, respectively. However, the combined fraction of cis-DCE and VC in the total chlorinated ethenes (PCE, TCE, cis-DCE and VC) increased from 73% to 98% and from 62% to 98%, respectively, which supports the notion that biological dechlorination of PCE and TCE was active. It is proposed that CMC-stabilized ZVI-Pd nanoparticles facilitated the early stage rapid abiotic degradation. Over the long run, the existing biological degradation process was boosted with CMC as the carbon source and hydrogen from the abiotic/biotic processes as the electron donor, resulting in the sustained enhanced destruction of the chlorinated organic chlorinated ethenes in the subsurface. PMID:20106501

  8. Interpretation of geophysical logs, aquifer tests, and water levels in wells in and near the North Penn Area 7 Superfund site, Upper Gwynedd Township, Montgomery County, Pennsylvania, 2000-02

    USGS Publications Warehouse

    Senior, Lisa A.; Cinotto, Peter J.; Conger, Randall W.; Bird, Philip H.; Pracht, Karl A.

    2005-01-01

    high-angle fractures and bedding-plane openings throughout the depth of the boreholes. Heatpulse-flowmeter measurements under nonpumping, ambient conditions indicated that borehole flow, where detected, was in the upward direction in three of the eight wells and in the downward direction in three wells. In two wells, both upward and downward flow were measured. Heatpulse-flowmeter measurements under pumping conditions were used to identify the most productive intervals in wells. Correlation of natural-gamma-ray and single-point-resistance logs indicated that bedding in the area probably strikes about 40 degrees northeast and dips from 6 to 7 degrees northwest. Aquifer intervals isolated by inflatable packers in wells were pumped to test productivity and to collect samples to determine chemical quality of water produced from the interval. Interval-isolation testing confirmed the presence of vertical hydraulic gradients indicated by heatpulse-flowmeter measurements. The specific capacities of isolated intervals ranged over two orders of magnitude, from 0.02 to more than 3.6 gallons per minute per foot. Intervals adjacent to isolated pumped intervals showed little response to pumping the isolated zone. The presence of vertical hydraulic gradients and lack of adjacent-interval response to pumping in isolated intervals indicate a limited degree of vertical hydraulic connection between the aquifer intervals tested. Concentrations of most VOC contaminants generally were highest in well-water samples from the shallowest isolated intervals, with some exceptions. Trichloroethylene, cis-1,2-dichloroethylene, and toluene were the most frequently detected VOCs, with maximum concentrations of greater than 340, 680, and greater than 590 micrograms per liter, respectively. Results of the aquifer test with multiple observation wells showed that water levels in 4 of the 14 wells declined in response to pumping. The four wells that responded to pumping are either along str

  9. Occurrence of Selected Organic Compounds in Groundwater Used for Public Supply in the Plio-Pleistocene Deposits in East-Central Nebraska and the Dawson and Denver Aquifers near Denver, Colorado, 2002-2004

    USGS Publications Warehouse

    Bails, Jeffrey B.; Dietsch, Benjamin J.; Landon, Matthew K.; Paschke, Suzanne S.

    2009-01-01

    ), which were detected in 9 of the 15 wells (60 percent of the samples). The second most frequently detected organic compound was tetrachloroethylene, detected in 4 of the 15 wells (27 percent of the samples), followed by chloroform, trichloroethylene, and 2-hydroxyatrazine (2-hydroxy-4-isopropylamino-6-ethylamino-s-triazine, or OIET), present in 3 of the 15 wells (20 percent of the samples). The pesticide compounds deisopropylatrazine (2-chloro-6-ethylamino-4-amino-s-triazine, or CEAT), metolachlor, and simazine and the volatile organic compound cis-1,2-dichloroethylene were detected in 2 of the 15 wells, and the compounds diuron and 1,2-dichloroethane were detected in only 1 of the 15 wells during the first-year sampling. Most detections of these compounds were at or near the minimum reporting levels, and none were greater than their regulatory maximum contaminant level. There were few detections of organic compounds during the first year of sampling groundwater wells in the South Platte study area. The compounds atrazine, deethylatrazine, picloram, tetrachloroethylene, methyl-tert-butyl-ether (MTBE), tris(2-butoxyethyl)phosphate, and bromoform were detected only once in all the samples from the 12 wells. Most detections of these compounds were at or near the minimum reporting levels, and none were greater than their regulatory maximum contaminant level. Second-year sampling, which included the addition of paired source- and finished-water samples, was completed at two sites in the High Plains study area. Source-water samples from the second-year sampling had detections of atrazine and deethylatrazine; at one site deisopropylatrazine and chloroform also were detected. The finished-water samples, which represent the source water after blending with water from other wells and treatment, indicated a decrease in the concentrations of the pesticides at one site, whereas concentrations remained nearly constant at a second site. The trihalomethanes (THMs or disinfec

  10. Long Term Leaching of Chlorinated Solvents from Source Zones in Low Permeability Settings with Fractures

    NASA Astrophysics Data System (ADS)

    Bjerg, P. L.; Chambon, J.; Troldborg, M.; Binning, P. J.; Broholm, M. M.; Lemming, G.; Damgaard, I.

    2008-12-01

    Groundwater contamination by chlorinated solvents, such as perchloroethylene (PCE), often occurs via leaching from complex sources located in low permeability sediments such as clayey tills overlying aquifers. Clayey tills are mostly fractured, and contamination migrating through the fractures spreads to the low permeability matrix by diffusion. This results in a long term source of contamination due to back-diffusion. Leaching from such sources is further complicated by microbial degradation under anaerobic conditions to sequentially form the daughter products trichloroethylene, cis-dichloroethylene (cis-DCE), vinyl chloride (VC) and ethene. This process can be enhanced by addition of electron donors and/or bioaugmentation and is termed Enhanced Reductive Dechlorination (ERD). This work aims to improve our understanding of the physical, chemical and microbial processes governing source behaviour under natural and enhanced conditions. That understanding is applied to risk assessment, and to determine the relationship and time frames of source clean up and plume response. To meet that aim, field and laboratory observations are coupled to state of the art models incorporating new insights of contaminant behaviour. The long term leaching of chlorinated ethenes from clay aquitards is currently being monitored at a number of Danish sites. The observed data is simulated using a coupled fracture flow and clay matrix diffusion model. Sequential degradation is represented by modified Monod kinetics accounting for competitive inhibition between the chlorinated ethenes. The model is constructed using Comsol Multiphysics, a generic finite- element partial differential equation solver. The model is applied at two well characterised field sites with respect to hydrogeology, fracture network, contaminant distribution and microbial processes (lab and field experiments). At the study sites (Sortebrovej and Vadsbyvej), the source areas are situated in a clayey till with fractures

  11. I{ Relationship between source clean up and mass flux of chlorinated solvents in low permeability settings with fractures}

    NASA Astrophysics Data System (ADS)

    Bjerg, P. L.; Chambon, J. C.; Christiansen, C. M.; Broholm, M. M.; Binning, P. J.

    2009-04-01

    Groundwater contamination by chlorinated solvents, such as perchloroethylene (PCE), often occurs via leaching from complex sources located in low permeability sediments such as clayey tills overlying aquifers. Clayey tills are mostly fractured, and contamination migrating through the fractures spreads to the low permeability matrix by diffusion. This results in a long term source of contamination due to back-diffusion. Leaching from such sources is further complicated by microbial degradation under anaerobic conditions to sequentially form the daughter products trichloroethylene, cis-dichloroethylene (cis-DCE), vinyl chloride (VC) and ethene. This process can be enhanced by addition of electron donors and/or bioaugmentation and is termed Enhanced Reductive Dechlorination (ERD). This work aims to improve our understanding of the physical, chemical and microbial processes governing source behaviour under natural and enhanced conditions. That understanding is applied to risk assessment, and to determine the relationship and time frames of source clean up and plume response. To meet that aim, field and laboratory observations are coupled to state of the art models incorporating new insights of contaminant behaviour. The long term leaching of chlorinated ethenes from clay aquitards is currently being monitored at a number of Danish sites. The observed data is simulated using a coupled fracture flow and clay matrix diffusion model. Sequential degradation is represented by modified Monod kinetics accounting for competitive inhibition between the chlorinated ethenes. The model is constructed using Comsol Multiphysics, a generic finite- element partial differential equation solver. The model is applied at well characterised field sites with respect to hydrogeology, fracture network, contaminant distribution and microbial processes (lab and field experiments). At one of the study sites (Sortebrovej), the source areas are situated in a clayey till with fractures and

  12. Ground-water-quality assessment of the Central Oklahoma aquifer, Oklahoma; hydrologic, water-quality, and quality-assurance data 1987-90

    USGS Publications Warehouse

    Ferree, D.M.; Christenson, S.C.; Rea, A.H.; Mesander, B.A.

    1992-01-01

    , ranging from below the reporting level to concentrations over the Maximum Contaminant Levels for several constituents (arsenic, barium, cadmium, chromium, lead, and selenium). Radionuclide activities also were highly variable. Gross alpha radioactivity ranged from 0.1 to 210 picocuries per liter as 230thorium. Of the wells sampled, 20 percent exceeded the proposed Maximum Contaminant Level of 15 picocuries per liter for gross alpha radioactivity. Organic constituents were detected in 39 percent of the 170 wells sampled for organic constituents; in most cases concentrations were at or near the laboratory minimum reporting levels. Ten of the wells sampled for organic constituents had one or more constituents (chlordane, dieldrin, heptachlor epoxide, trichloroethylene, 1,1-dichloroethylene, 1,1,1-trichloroethane) at concentrations equal to or greater than the Maximum Contaminant Level or acceptable concentrations as suggested in the Environmental Protection Agency's Health Advisory Summaries. Quality-assurance sampling included duplicate samples, repeated samples, blanks, spikes, and blind samples. These samples proved to be essential in evaluating the accuracy of the data, particularly in the case of volatile organic constituents.

  13. Hanford Site Groundwater Monitoring for Fiscal Year 1999

    SciTech Connect

    MJ Hartman; LF Morasch; WD Webber

    2000-05-10

    This report presents the results of groundwater and vadose zone monitoring and remediation for fiscal year 1999 on the US. Department of Energy's Hanford Site, Washington. Water-level monitoring was performed to evaluate groundwater flow directions, to track changes in water levels, and to relate such changes to evolving disposal practices. Measurements for site-wide maps were conducted in June in past years and are now measured in March to reflect conditions that are closer to average. Water levels over most of the Hanford Site continued to decline between June 1998 and March 1999. The most widespread radiological contaminant plumes in groundwater were tritium and iodine-129. Concentrations of carbon-14, strontium-90, technetium-99, and uranium also exceeded drinking water standards in smaller plumes. Cesium-137 and plutonium exceeded standards only near the 216-B-5 injection well. Derived concentration guide levels specified in US Department of Energy Order 5400.5 were exceeded for plutonium, strontium-90, tritium, and uranium in small plumes or single wells. Nitrate and carbon tetrachloride are the most extensive chemical contaminants. Chloroform, chromium, cis-1,2dichloroethylene, cyanide, fluoride, and trichloroethylene also were present in smaller areas at levels above their maximum contaminant levels. Metals such as aluminum, cadmium, iron, manganese, and nickel exceeded their maximum contaminant levels in filtered samples from numerous wells; however, in most cases, they are believed to represent natural components of groundwater. ''Resource Conservation and Recovery Act of 1976'' groundwater monitoring continued at 25 waste management areas during fiscal year 1999: 16 under detection programs and data indicate that they are not adversely affecting groundwater; 6 under interim status groundwater quality assessment programs to assess contamination; and 2 under final status corrective-action programs. Another site, the 120-D-1 ponds, was clean closed in

  14. Assessment of Hyporheic Zone, Flood-Plain, Soil-Gas, Soil, and Surface-Water Contamination at the McCoys Creek Chemical Training Area, Fort Gordon, Georgia, 2009-2010

    USGS Publications Warehouse

    Guimaraes, Wladmir B.; Falls, W. Fred; Caldwell, Andral W.; Ratliff, W. Hagan; Wellborn, John B.; Landmeyer, James E.

    2011-01-01

    The U.S. Geological Survey, in cooperation with the U.S. Department of the Army Environmental and Natural Resources Management Office of the U.S. Army Signal Center and Fort Gordon, Georgia, assessed the hyporheic zone, flood plain, soil gas, soil, and surface water for contaminants at the McCoys Creek Chemical Training Area (MCTA) at Fort Gordon, from October 2009 to September 2010. The assessment included the detection of organic contaminants in the hyporheic zone, flood plain, soil gas, and surface water. In addition, the organic contaminant assessment included the analysis of organic compounds classified as explosives and chemical agents in selected areas. Inorganic contaminants were assessed in soil and surface-water samples. The assessment was conducted to provide environmental contamination data to the U.S. Army at Fort Gordon pursuant to requirements of the Resource Conservation and Recovery Act Part B Hazardous Waste Permit process. Ten passive samplers were deployed in the hyporheic zone and flood plain, and total petroleum hydrocarbons (TPH) and octane were detected above the method detection level in every sampler. Other organic compounds detected above the method detection level in the hyporheic zone and flood-plain samplers were trichloroethylene, and cis- and trans- 1, 2-dichloroethylene. One trip blank detected TPH below the method detection level but above the nondetection level. The concentrations of TPH in the samplers were many times greater than the concentrations detected in the blank; therefore, all other TPH concentrations detected are considered to represent environmental conditions. Seventy-one soil-gas samplers were deployed in a grid pattern across the MCTA. Three trip blanks and three method blanks were used and not deployed, and TPH was detected above the method detection level in two trip blanks and one method blank. Detection of TPH was observed at all 71 samplers, but because TPH was detected in the trip and method blanks, TPH was

  15. Probabilistic Health Risk Assessment of Chemical Mixtures: Importance of Travel Times and Connectivity

    NASA Astrophysics Data System (ADS)

    Henri, Christopher V.; Fernàndez-Garcia, Daniel; de Barros, Felipe P. J.

    2014-05-01

    Subsurface contamination cases giving rise to groundwater pollutions are extensively found in all industrialized countries. Under this pressure, risk assessment methods play an important role in population protection by (1) quantifying the potential impact on human health of an aquifer contamination and (2) helping and driving decisions of groundwater-resource managers. Many reactive components such as chlorinated solvents or nitrates potentially experience attenuation processes under common geochemical conditions. This represents an attractive and extensively used remediation solution but leads often to the production of by-products before to reach a harmless chemical form. This renders mixtures of contaminants a common issue for groundwater resources managers. In this case, the threat posed by these contaminants to human health at a given sensitive location greatly depends on the competition between reactive and advective-dispersive characteristic times. However, hydraulic properties of the aquifer are known to be spatially variable, which can lead to the formation of preferential flow channels and fast contamination pathways. Therefore, the uncertainty on the spatial distribution of the aquifer properties controlling the plume travel time may then play a particular role in the human health risk assessment of chemical mixtures. We investigate here the risk related to a multispecies system in response to different degrees of heterogeneity of the hydraulic conductivity (K or Y =ln(K)). This work focuses on a Perchloroethylene (PCE) contamination problem followed by the sequential first-order production/biodegradation of its daughter species Trichloroethylene (TCE), Dichloroethylene (DCE) and Vinyl Chlorine (VC). For this specific case, VC is known to be a highly toxic contaminant. By performing numerical experiments, we evaluate transport through three-dimensional mildly (σY 2=1.0) and highly (σY 2=4.0) heterogeneous aquifers. Uncertainty on the hydraulic

  16. Hanford Site Groundwater Monitoring for Fiscal Year 1998

    SciTech Connect

    Hartman, M.J.

    1999-03-24

    This report presents the results of groundwater and vadose-zone monitoring and remediation for fiscal year (FY) 1998 on the Word Site, Washington. Soil-vapor extraction in the 200-West Area removed 777 kg of carbon tetrachloride in FY 1998, for a total of 75,490 kg removed since remediation began in 1992. Spectral gamma logging and evaluation of historical gross gamma logs near tank farms and liquid-disposal sites in the 200 Areas provided information on movement of contaminants in the vadose zone. Water-level monitoring was performed to evaluate groundwater-flow directions, to track changes in water levels, and to relate such changes to evolving disposal practices. Water levels over most of the Hanford Site continued to decline between June 1997 and June 1998. The most widespread radiological contaminant plumes in groundwater were tritium and iodine-129. Concentrations of technetium-99, uranium, strontium-90, and carbon-14 also exceeded drinking water standards in smaller plumes. Plutonium and cesium-137 exceeded standards only near the 216-B-5 injection well. Derived concentration guide levels specified in U.S. Department of Energy Order 5400.5 were exceeded for tritium, uranium, strontium-90, and plutonium in small plumes or single wells. One well completed in the basalt-confined aquifer beneath the 200-East Area exceeded the drinking water standard for technetium-99. Nitrate is the most extensive chemical contaminant. Carbon tetrachloride, chloroform, chromium, cis-l, Z-dichloroethylene, fluoride, and trichloroethylene also were present in smaller areas at levels above their maximum contaminant levels. Cyanide concentrations were elevated in one area but were below the maximum contaminant level. Tetrachloroethylene exceeded its maximum contaminant level in several wells in the 300 Area for the first time since the 1980s. Metals such as aluminum, cadmium, iron, manganese, and nickel exceeded their maximum contaminant levels in filtered samples from numerous

  17. Hydrogeology and water quality of a surficial aquifer underlying an urban area, Manchester, Connecticut

    USGS Publications Warehouse

    Mullaney, John R.; Grady, Stephen J.

    1997-01-01

    The quality of water along flowpaths in a surficial aquifer system in Manchester, Connecticut, was studied during 1993-95 as part of the National Water Quality Assessment program. The flowpath study examined the relations among hydrogeology, land-use patterns, and the presence of contaminants in a surficial aquifer in an urban area, and evaluated ground water as a source of contamination to surface water. A two-dimensional, finite-difference groundwater- flow model was used to estimate travel distance, which ranged from about 50 to 11,000 feet, from the source areas to the sampled observation wells. Land use, land cover, and population density were determined in the source areas delineated by the ground-water-flow simulation. Source areas to the wells contained either high- or medium-density residential areas, and population density ranged from 629 to 8,895 people per square mile. Concentrations of selected inorganic constituents, including sodium, chloride, and nitrite plus nitrate nitrogen, were higher in the flowpath study wells than in wells in undeveloped areas with similar aquifer materials. One or more of 9 volatile organic compounds were detected at 12 of 14 wells. The three most commonly detected volatile organic compounds were chloroform, methyl-tert-butyl ether, and trichloroethene. Trichloroethene was detected at concentrations greater than the maximum contaminant level for drinking water (5 micrograms per liter) in samples from one well. Four pesticides, including dichloro diphenyl dichloroethylene, dieldrin, dichloroprop, and simazine were detected at low concentrations. Concentrations of sodium and chloride were higher in samples collected from wells screened in the top of the saturated zone than in samples collected from deeper zones. Volatile organic compounds and elevated concentrations of nitrite plus nitrate as nitrogen were detected at depths of as much as 60 feet below the water table, indicating that the effects of human activities on the

  18. Monitoring the decontamination of a site polluted by DNAPLs

    NASA Astrophysics Data System (ADS)

    Audí-Miró, C.; Espinola, R.; Torrentó, C.; Otero, N.; Rossi, A.; Palau, J.; Soler, A.

    2012-04-01

    The aim of this study is to monitor the decontamination of a site polluted by DNAPLs coming from an automotive industry. The contamination was caused by the poor management of the waste generated by the industrial activity, which was discharged into a seepage pit. As a result, soil contamination was produced in the seepage pit area and a plume of DNAPLs-contaminated groundwater was generated. To recover the original environmental quality, a dual action was proposed: in the first place, the removal of the source of contamination and in the second one, the treatment of the DNAPLs plume. The elimination of the source of contamination consisted on a selective excavation of the seepage pit and an offsite management of the contaminated land. To restore the groundwater quality, a passive treatment system using a permeable reactive barrier (PRB) of zero valent iron (ZVI) was implemented. In order to determine the efficiency of the remediation actions, a chemical, isotopic and hydrogeological control of the main solvents detected in groundwater (perchloroethylene -PCE-, trichloroethene -TCE- and cis-dichloroethylene -cis-DCE-) has been established. Results show a decrease in PCE concentration that has been attributed to the removal of the source more than to a degradation process. However, the presence of PCE by-products, TCE and cis-DCE, might indicate a possible PCE biotic degradation. δ13CPCE values analyzed upstream and downstream of the barrier don't show isotopic changes associated to the PRB (values are around -20‰ in all the sampling points). TCE might have experienced a natural advanced degradation process according to the high concentration of cis-DCE found prior the installation of the PRB and the isotopic enrichment in δ13CTCE in some specific areas of the plume (-19.9‰ in the source and -16‰ before the barrier). Slight isotopic changes have been observed in the water flow in a far distance after the barrier (-15.4‰). δ13Ccis-DCE experienced an

  19. Hydrogeology, water chemistry, and transport processes in the zone of contribution of a public-supply well in Albuquerque, New Mexico, 2007-9

    USGS Publications Warehouse

    Bexfield, Laura M.; Jurgens, Bryant C.; Crilley, Dianna M.; Christenson, Scott C.

    2012-01-01

    (TCE) and cis-1,2-dichloroethylene had been detected in the SSW, and several of these wells m