Adipose tissue concentrations of PCB, HCB, chlordane, PBDE and P,P'-DDE and the risk for endometrial cancer

Energy Technology Data Exchange (ETDEWEB)

Lindstroem, G.; Bavel, B. van; Bjoernfoth, H. [MTM Research Centre, Oerebro Univ., Oerebro (Sweden); Hardell, L. [Dept. of Oncology, Univ. Hospital, Oerebro (Sweden)

2004-09-15

Environmental pollutants with hormonal activity, such as xenoestrogens, have for several years been of concern as potential risk factors for hormone dependant tumors. Impacts of increasing levels of xenoestrogens have been observed in aquatic organisms. In humans concern has been focused on ''endocrine disrupting chemicals'' with either estrogenic or antiestrogenic activities. Some persistent organic pollutants (POPs) such as polychlorinated biphenyls (PCBs), and especially the hydroxylated metabolites, and chlordanes, have been postulated to be endocrine disruptors. PCBs have been shown to reverse gonadal sex in turtle5 and abnormalities of reproductive development has been described in juvenile alligators living in contaminated environment in Florida. Hexachlorobenzene (HCB) has been shown to have endocrine-disrupting properties. Also p,p'-dichlorodiphenyl-dichloroethylene (p,p'-DDE) the most persistent metabolite of p,p'-DDT has been postulated to be an environmental endocrine disruptor. In a case-control study on patients with testicular cancer we found higher concentrations of PCBs, HCB and chlordanes in mothers to cases than in mothers to controls. Similar concentrations were found in cases with testicular cancer as in the population controls. The study gave support to the hypothesis that exposure to endocrine disruptors during the fetal period may be of etiologic importance in the etiology of testicular cancer. Another hormone dependent cancer is endometrial cancer. It accounted for 5.8% of all cancers incidents among Swedish women in 2002. The cumulative probability of developing the disease before 85 years of age was 2.8% in 2002. Estrogen replacement has been suggested as a risk factor among several others. The first cases of endometrial cancer among women using estrogen replacement therapy were reported in early 1960's. Is there a relationship between levels of POPs and incidence rate? The aim is to investigate

Electronically excited negative ion resonant states in chloroethylenes

Energy Technology Data Exchange (ETDEWEB)

Khvostenko, O.G., E-mail: khv@mail.ru; Lukin, V.G.; Tuimedov, G.M.; Khatymova, L.Z.; Kinzyabulatov, R.R.; Tseplin, E.E.

2015-02-15

Highlights: • Several novel dissociative negative ion channels were revealed in chloroethylenes. • The electronically excited resonant states were recorded in all chloroethylenes under study. • The states were assigned to the inter-shell types, but not to the core-excited Feshbach one. - Abstract: The negative ion mass spectra of the resonant electron capture by molecules of 1,1-dichloroethylene, 1,2-dichloroethylene-cis, 1,2-dichloroethylene-trans, trichloroethylene and tetrachloroethylene have been recorded in the 0–12 eV range of the captured electron energy using static magnetic sector mass spectrometer modified for operation in the resonant electron capture regime. As a result, several novel low-intensive dissociation channels were revealed in the compounds under study. Additionally, the negative ion resonant states were recorded at approximately 3–12 eV, mostly for the first time. These resonant states were assigned to the electronically excited resonances of the inter-shell type by comparing their energies with those of the parent neutral molecules triplet and singlet electronically excited states known from the energy-loss spectra obtained by previous studies.

Evaluation of in-situ methanotrophic bioremediation for contaminated groundwater, St. Joseph, Michigan. Final report, January 1989-December 1989

International Nuclear Information System (INIS)

McCarty, P.L.; Semprini, L.; Dolan, M.E.; Harmon, T.C.; Just, S.

1990-09-01

A feasibility study of utilizing indigenous bacteria that use methane as a source of cell carbon and energy (methanotrophs) for in-situ bioremediation of groundwater contaminants at the St. Joseph site is summarized. The contaminants, compounds, can be biotransformed by methanotrophic bacteria, which are found in some locations of the site in adequate populations. The process involves stimulating the growth of native populations of methanotrophs by injecting water containing dissolved methane and oxygen into the aquifer. The stimulated population of methanotrophs in turn has the capability to degrade trichloroethylene, 1,2-cis-dichloroethylene, 1,2-trans-dichloroethylene, and vinyl chloride

21 CFR 177.1655 - Polysulfone resins.

Science.gov (United States)

2010-04-01

... disodium salt of 4,4′-isopropylidenediphenol is made to react with 4,4′-dichlorodiphenyl sulfone in such a... Limitations Dimethyl sulfoxide Not to exceed 50 parts per million as residual solvent in finished basic resin... residual solvent in finished basic resin in paragraph (a)(1) of this section. N-methyl-2-pyrrolidone Not to...

Determination of volatile organic hydrocarbons in water samples by solid-phase dynamic extraction

Energy Technology Data Exchange (ETDEWEB)

Jochmann, Maik A.; Schmidt, Torsten C. [Eberhard-Karls-Universitaet Tuebingen, Center for Applied Geoscience (ZAG), Tuebingen (Germany); Chair of Instrumental Analysis, University Duisburg-Essen, Duisburg (Germany); Yuan, Xue [Eberhard-Karls-Universitaet Tuebingen, Center for Applied Geoscience (ZAG), Tuebingen (Germany)

2007-03-15

In the present study a headspace solid-phase dynamic extraction method coupled to gas chromatography-mass spectrometry (HS-SPDE-GC/MS) for the trace determination of volatile halogenated hydrocarbons and benzene from groundwater samples was developed and evaluated. As target compounds, benzene as well as 11 chlorinated and brominated hydrocarbons (vinyl chloride, dichloromethane, cis-1,2-dichloroethylene, trans-1,2-dichloroethylene, carbon tetrachloride, chloroform, trichloroethylene, tetrachloroethylene, bromoform) of environmental and toxicological concern were included in this study. The analytes were extracted using a SPDE needle device, coated with a poly(dimethylsiloxane) with 10% embedded activated carbon phase (50-{mu}m film thickness and 56-mm film length) and were analyzed by GC/MS in full-scan mode. Parameters that affect the extraction yield such as extraction and desorption temperature, salting-out, extraction and desorption flow rate, extraction volume and desorption volume, the number of extraction cycles, and the pre-desorption time have been evaluated and optimized. The linearity of the HS-SPDE-GC/MS method was established over several orders of magnitude. Method detection limits (MDLs) for the compounds investigated ranged between 12 ng/L for cis-dichloroethylene and trans-dichloroethylene and 870 ng/L for vinyl chloride. The method was thoroughly validated, and the precision at two concentration levels (0.1 mg/L and a concentration 5 times above the MDL) was between 3.1 and 16% for the analytes investigated. SPDE provides high sensitivity, short sample preparation and extraction times and a high sample throughput because of full automation. Finally, the applicability to real environmental samples is shown exemplarily for various groundwater samples from a former waste-oil recycling facility. Groundwater from the site showed a complex contamination with chlorinated volatile organic compounds and aromatic hydrocarbons. (orig.)

Determination of volatile organic hydrocarbons in water samples by solid-phase dynamic extraction.

Science.gov (United States)

Jochmann, Maik A; Yuan, Xue; Schmidt, Torsten C

2007-03-01

In the present study a headspace solid-phase dynamic extraction method coupled to gas chromatography-mass spectrometry (HS-SPDE-GC/MS) for the trace determination of volatile halogenated hydrocarbons and benzene from groundwater samples was developed and evaluated. As target compounds, benzene as well as 11 chlorinated and brominated hydrocarbons (vinyl chloride, dichloromethane, cis-1,2-dichloroethylene, trans-1,2-dichloroethylene, carbon tetrachloride, chloroform, trichloroethylene, tetrachloroethylene, bromoform) of environmental and toxicological concern were included in this study. The analytes were extracted using a SPDE needle device, coated with a poly(dimethylsiloxane) with 10% embedded activated carbon phase (50-microm film thickness and 56-mm film length) and were analyzed by GC/MS in full-scan mode. Parameters that affect the extraction yield such as extraction and desorption temperature, salting-out, extraction and desorption flow rate, extraction volume and desorption volume, the number of extraction cycles, and the pre-desorption time have been evaluated and optimized. The linearity of the HS-SPDE-GC/MS method was established over several orders of magnitude. Method detection limits (MDLs) for the compounds investigated ranged between 12 ng/L for cis-dichloroethylene and trans-dichloroethylene and 870 ng/L for vinyl chloride. The method was thoroughly validated, and the precision at two concentration levels (0.1 mg/L and a concentration 5 times above the MDL) was between 3.1 and 16% for the analytes investigated. SPDE provides high sensitivity, short sample preparation and extraction times and a high sample throughput because of full automation. Finally, the applicability to real environmental samples is shown exemplarily for various groundwater samples from a former waste-oil recycling facility. Groundwater from the site showed a complex contamination with chlorinated volatile organic compounds and aromatic hydrocarbons.

Electronically excited states of chloroethylenes: Experiment and DFT calculations in comparison

International Nuclear Information System (INIS)

Khvostenko, O.G.

2014-01-01

Highlights: • B3LYP/6-311 + G(d,p) calculations of chloroethylenes molecules were performed. • Calculations were correlated with experiment on the molecules ground and excited states. • The general pattern of electron structure of chloroethylenes was obtained. • Necessity of this data for chloroethylenes negative ions study was noted. - Abstract: B3LYP/6-311 + G(d,p) calculations of ground and electronically excited states of ethylene, chloroethylene, 1,1-dichloroethylene, 1,2-dichloroethylene-cis, 1,2-dichloroethylene-trans trichloroethylene and tetrachloroethylene molecules have been performed. Molecular orbitals images and orbital correlation diagram are given. The calculation results for chloroethylenes electronically excited states were compared with experimental data from the energy-loss spectra obtained and generally considered previously by C.F. Koerting, K.N. Walzl and A. Kupperman. Several new additional triplet and singlet transitions were pointed out in these spectra considering the calculation results. The finding of the additional transitions was supported by the UV absorption spectrum of trichloroethylene recorded in big cuvette (10 cm), where the first three triplet and two low-intensive forbidden singlet transitions were registered. The first triplet of this compound was recorded to be at the same energy as was found with the energy-loss spectroscopy

Electronically excited states of chloroethylenes: Experiment and DFT calculations in comparison

Energy Technology Data Exchange (ETDEWEB)

Khvostenko, O.G., E-mail: khv@mail.ru

2014-08-15

Highlights: • B3LYP/6-311 + G(d,p) calculations of chloroethylenes molecules were performed. • Calculations were correlated with experiment on the molecules ground and excited states. • The general pattern of electron structure of chloroethylenes was obtained. • Necessity of this data for chloroethylenes negative ions study was noted. - Abstract: B3LYP/6-311 + G(d,p) calculations of ground and electronically excited states of ethylene, chloroethylene, 1,1-dichloroethylene, 1,2-dichloroethylene-cis, 1,2-dichloroethylene-trans trichloroethylene and tetrachloroethylene molecules have been performed. Molecular orbitals images and orbital correlation diagram are given. The calculation results for chloroethylenes electronically excited states were compared with experimental data from the energy-loss spectra obtained and generally considered previously by C.F. Koerting, K.N. Walzl and A. Kupperman. Several new additional triplet and singlet transitions were pointed out in these spectra considering the calculation results. The finding of the additional transitions was supported by the UV absorption spectrum of trichloroethylene recorded in big cuvette (10 cm), where the first three triplet and two low-intensive forbidden singlet transitions were registered. The first triplet of this compound was recorded to be at the same energy as was found with the energy-loss spectroscopy.

In vitro mutagenicity and genotoxicity study of 1,2-dichloroethylene, 1,1,2-trichloroethane, 1,3-dichloropropane, 1,2,3-trichloropropane and 1,1,3-trichloropropene, using the micronucleus test and the alkaline single cell gel electrophoresis technique (comet assay) in human lymphocytes.

Science.gov (United States)

Tafazoli, M; Kirsch-Volders, M

1996-12-20

The main objective of this study was to compare the cytotoxic genotoxic and mutagenic activity of a number of chlorinated aliphatic hydrocarbons, which are widely used as chemical intermediates, solvents, degreasing agents etc. in industry, and to establish the structure-toxicity relationship of the chemicals by using the most adequate determinants in estimating their toxicity. The mutagenicity and cytotoxicity of some of the candidate chemicals, namely 1,2-dichloroethylene, 1,1,2-trichloroethane, 1,3-dichloropropane, 1,2,3-trichloropropane and 1,1,3-trichloropropene were evaluated in an in vitro micronucleus assay. The cytokinesis-block methodology was applied on human lymphocytes in the presence or absence of an external metabolic activation system (S9-mix). In the micronucleus assay, all test substances, except 1,2,3-trichloropropane with and without S9-mix and 1,1,2-trichloroethane without S9-mix in the repeated experiment, exhibited a low but statistically significant mutagenic activity, compared to the concurrent control. However, none of the five chemicals was able to induce a clear and reproducible linear dose-dependent increase in micronucleus frequencies in this assay. Generally, mutagenic activity of the chemicals was found in the absence of severe cytotoxicity and/or cell cycle delay. The DNA breakage capacity and the cytotoxicity of these chemicals were also assessed in the alkaline single cell gel (SCG) electrophoresis test (comet assay) with and without S9-mix in isolated human lymphocytes. All chemical compounds induced DNA breakage, in the presence or absence of the metabolic activation system, at the doses tested. The data showed that the DNA reactivity of the chemicals increased with increasing degree of halogenation. The results of the present work suggested that the comet assay might be a more suitable and sensitive screening method than the micronucleus test for this particular class of compound. However, both assays do detect different

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

Science.gov (United States)

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...

Phytoscreening for vinyl chloride in groundwater discharging to a stream

DEFF Research Database (Denmark)

Ottosen, Cecilie Bang; Rønde, Vinni Kampman; Trapp, Stefan

2018-01-01

and hence different uptake/loss scenarios. Vinyl chloride (VC) as well as cis-dichloroethylene (cis-DCE), trichloroethylene (TCE), and tetrachloroethylene (PCE) were detected in the trees, documenting that phytoscreening is a viable method to locate chlorinated ethene plumes, including VC, discharging...

Altered developmental timing in early life stages of Antarctic krill (Euphausia superba) exposed to p,p'-DDE

Energy Technology Data Exchange (ETDEWEB)

Poulsen, Anita H., E-mail: anita.poulsen@uq.edu.au [The University of Queensland, National Research Centre for Environmental Toxicology (Entox), 39 Kessels Rd, Brisbane, Qld 4108 (Australia); Kawaguchi, So, E-mail: so.kawaguchi@aad.gov.au [Australian Antarctic Division, Channel Highway, Kingston, Tas 7050 (Australia); Leppaenen, Matti T., E-mail: matti.t.leppanen@uef.fi [University of Eastern Finland, Joensuu Campus, Department of Biology, FIN-80101 (Finland); Kukkonen, Jussi V.K., E-mail: jussi.kukkonen@uef.fi [University of Eastern Finland, Joensuu Campus, Department of Biology, FIN-80101 (Finland); Bengtson Nash, Susan M., E-mail: s.bengtsonnash@griffith.edu.au [The University of Queensland, National Research Centre for Environmental Toxicology (Entox), 39 Kessels Rd, Brisbane, Qld 4108 (Australia); Griffith University, Atmospheric Environment Research Centre, Brisbane, Qld 4111 (Australia)

2011-11-15

Persistent organic pollutants (POPs) are persistent, toxic and bioaccumulative anthropogenic organic chemicals, capable of undergoing long range environmental transport to remote areas including the Antarctic. p,p'-dichlorodiphenyl dichloroethylene (p,p'-DDE) has been identified as a dominant POP accumulating in Antarctic krill (Euphausia superba), which is a key Southern Ocean species. This study examined the developmental toxicity of p,p'-DDE via aqueous exposure to Antarctic krill larvae. p,p'-DDE exposure was found to stimulate developmental timing in the first three larval stages of Antarctic krill, while extended monitoring of larvae after a five day exposure period had ended, revealed delayed inhibitory responses during development to the fourth larval stage. Stimulatory responses were observed from the lowest p,p'-DDE body residue tested of 10.1 {+-} 3.0 {mu}mol/kg (3.2 {+-} 0.95 mg/kg) preserved wet weight, which is comparable to findings for temperate species and an order of magnitude lower than the exposure level found to cause sublethal behavioural effects in Antarctic krill. The delayed responses included increased mortality, which had doubled in the highest p,p'-DDE treatment (95 {+-} 8.9% mortality at 20 {mu}g/L p,p'-DDE) compared to the solvent control (44 {+-} 11% mortality) 2 weeks after end of exposure. Development of surviving metanauplius larvae to calyptopis 1 larvae was delayed by 2 days in p,p'-DDE exposed larvae compared with untreated larvae. Finally, the developmental success of surviving p,p'-DDE exposed larvae was reduced by 50 to 75% compared to the solvent control (100% developmental success). The lowest observed effect concentration for all delayed effects was 1 {mu}g/L, the lowest exposure concentration tested. These findings demonstrate the importance of delayed and indirect effects of toxicant exposure. Further, the findings of this study are important for environmental risk assessment

77 FR 43529 - National Oil and Hazardous Substances Pollution Contingency Plan; National Priorities List...

Science.gov (United States)

2012-07-25

... health and the environment, which may result if the contamination associated with the Dix Area Sanitary... media (air, surface water, sediment, soil, and groundwater). During the evaluation of site risks...- dichloroethylene, 1,1,1-trichloroethane, ethylbenzene, nickel, mercury, cadmium, zinc, chromium, and manganese...

77 FR 20585 - Proposed Withdrawal of Certain Federal Water Quality Criteria Applicable to California, New...

Science.gov (United States)

2012-04-05

...)). Nickel (aquatic life--freshwater (acute and chronic) and marine water (acute)). Selenium (aquatic life...) and marine water (chronic)). Nickel (aquatic life--marine water (chronic)). 1,1-Dichloroethylene...-reviewed studies and data that assess effects of early-life exposure to the toxic pollutants for which we...

Determination of adsorption isotherms of chlorinated hydrocarbons on halloysite adsorbent by inverse gas chromatography.

Science.gov (United States)

Czech, K; Słomkiewicz, P M

2013-05-03

Inverse gas chromatographic methods of isotherm determination peak maximum (PM) and peak division (PD) were compared. These methods were applied to determine adsorption isotherms of dichloroethylene, trichloroethylene and tetrachloroethylene on acid-activated halloysite and adsorption enthalpy. Copyright © 2013 Elsevier B.V. All rights reserved.

Trends in chemical concentration in sediment cores from three lakes in New Jersey and one lake on Long Island, New York

Science.gov (United States)

Long, Gary R.; Ayers, Mark A.; Callender, Edward; Van Metre, Peter C.

2003-01-01

Sediment cores were extracted from three lakes in northeastern New Jersey and one lake on western Long Island, New York, as part of the U.S. Geological Survey National Water-Quality Assessment Program. Sediment layers were dated by use of cesium-137 (137Cs), copper, lead, or dichlorodiphenyl-trichloroethane (DDT) profiles. Sediment layers were analyzed for seven selected trace elements, including arsenic, cadmium, chromium, lead, mercury, nickel, and zinc, and five hydrophobic organochlorine compounds, including chlordane, dieldrin, total DDT, total polychlorinated biphenyls (PCBs), and total polycyclic aromatic hydrocarbons (PAHs).

Sorption of chlorinated solvents and degradation products on natural clayey tills

DEFF Research Database (Denmark)

Cong, Lu; Bjerg, Poul Løgstrup; Zhang, Fengjun

2011-01-01

linear, but fitted by Freundlich isotherms slightly better over the entire concentration range. For chloroethylenes, tetrachloroethylene (PCE) was most strongly sorbed to the clayey till samples (Kd=0.84–2.45Lkg−1), followed by trichloroethylene (TCE, Kd=0.62–0.96Lkg−1), cis-dichloroethylene (cis-DCE, Kd...

76 FR 41719 - National Oil and Hazardous Substances Pollution Contingency Plan; National Priorities List...

Science.gov (United States)

2011-07-15

....regulations.gov or in hard copy at:U.S. EPA Record Center, 61 Forsyth Street, SW, Atlanta, GA 30303, Hours: 8..., chromium, 1,4-dichlorobenzene, trans-1,2- dichloroethylene, ethyl benzene, lead, naphthalene, and vinyl... attenuation mechanisms; (2) ensure that benzene and vinyl chloride concentrations continue to be below cleanup...

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

International Nuclear Information System (INIS)

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

Characterization of Chloroethylene Dehalogenation by Cell Extracts of Desulfomonile tiedjei and Its Relationship to Chlorobenzoate Dehalogenation

Science.gov (United States)

Townsend, G. T.; Suflita, J. M.

1996-01-01

We characterized the reductive dehalogenation of tetrachloroethylene in cell extracts of Desulfomonile tiedjei and compared it with this organism's 3-chlorobenzoate dehalogenation activity. Tetrachloroethylene was sequentially dehalogenated to trichloro- and dichloroethylene; there was no evidence for dichloroethylene dehalogenation. Like the previously characterized 3-chlorobenzoate dehalogenation activity, tetrachloroethylene dehalogenation was heat sensitive, not oxygen labile, and increased in proportion to the amount of protein in assay mixtures. In addition, both dehalogenation activities were dependent on hydrogen or formate as an electron donor and had an absolute requirement for either methyl viologen or triquat as an electron carrier in vitro. Both activities appear to be catalyzed by integral membrane proteins with similar solubilization characteristics. Dehalogenation of tetrachloroethylene was inhibited by 3-chlorobenzoate but not by the structural isomers 2- and 4-chlorobenzoate. The last two compounds are not substrates for D. tiedjei. These findings lead us to suggest that the dehalogenation of tetrachloroethylene in D. tiedjei is catalyzed by a dehalogenase previously thought to be specific for meta-halobenzoates. PMID:16535377

Health assessment for Westinghouse Elevator, Cumberland Township, Adams County, Pennsylvania, Region 3. CERCLIS No. PAD043882281. Preliminary report

Energy Technology Data Exchange (ETDEWEB)

1989-01-19

The Westinghouse Elevator site in Adams County, Pennsylvania has been in operation since 1968 as an elevator component manufacturing facility. During the process of elevator cab production, parts were passed through a degreasing and paint phase. Sampling of nearby surface water in 1983 revealed contamination with organic solvents. The environmental contamination on-site consists of 1,1,1-trichloroethane and trichloroethylene in surface sludge, soil, surface water, sediment, and groundwater. In addition, 1,1-dichloroethane and 1,1-dichloroethylene were detected in soil. The environmental contamination off-site consists of 1,1,1-trichloroethane, 1,1-dichloroethylene, 1,1-dichloroethane, and trichloroethylene in residential water supply wells. Contaminated groundwater is of primary importance to the site. Private wells have been found to be contaminated and alternate water supplies have been provided. One public supply well has been decommissioned due to contamination. 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, and possibly on-site soil.

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

International Nuclear Information System (INIS)

Chase, J.

2000-01-01

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

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

Energy Technology Data Exchange (ETDEWEB)

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.

Mixed Waste Management Facility (MWMF) groundwater monitoring report

International Nuclear Information System (INIS)

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

Odour Samples Degradation During Detention in Tedlar® Bags.

Science.gov (United States)

Szyłak-Szydłowski, Mirosław

In indirect olfactometry analysis, to avoid condensation or adsorption processes during or storage of the sample, containers made of suitable materials should be used. Also, reaction between the chemicals during transport from the source of the odour to the research laboratory is an important process which can influence on examinations' results. Study included determination of the odour and compound concentrations of six gas mixtures. Gas samples were collected by silicone hoses into Tedlar ® bags and tested by Nasal Ranger, SM-100 olfactometers and Photovac Voyager gas chromatograph. Time of keeping gas in bags was 78 h, and concentration of compounds was measured every hour, eight times per day. For benzene, acetone, 1,1-dichloroethylene, c-1,2-dichloroethylene, t-1,2-dichloroethylene, methyl ethyl ketone and vinyl chloride, 100 % decrease of concentration has been noticed within 78 h of holding in the bag. Average rate of loss of most compounds concentration was from 0.01 to 2.50 % for the first 30 h and from 0.35 to 18.50 % during the last 48 h of examination. Decreasing of odour concentration measured by Nasal Ranger (NR) in all series was between 0.00 and 4.98 % till 30 h, between 1.91 and 100 % in the last 48 h of test and between 1.61 and 100 % in 78 h. In case of odour concentration measured by SM, those values were, respectively, 1.26-4.93 %, 1.39-4.93 % and 2.40-3.18 %. Values of average rate of intensity decreasing were, respectively, 0.77-1.75 %, 2.36-4.67 % and 1.18-2.07 %. Statistically significant correlation coefficients for compound concentrations and intensity, odour concentration obtained by SM-100 as well as NR were, respectively, 0.55-0.97, 0.47-0.99 and 0.37-0.98.

Demonstration/Validation of the Snap Sampler

Science.gov (United States)

2011-06-01

Calcium Cd Cadmium cDCE cis,1,2-DCE Cl Chloride Co Cobalt Cr Chromium Cu Copper DCE Dichloroethylene Fe Iron K Potassium Mg Magnesium Mn...the original bottle in which they were collected, presumably losses of volatiles and changes in concentrations of dissolved gases or analytes...present across the zone, in part because of excavation and re- moval. This has resulted in hydraulically interconnected bedrock and overburden water

Xenoendocrine pollutants May Reduce Size of Sexual Organs in East Greenland Polar Bears (Ursus Maritimus)

DEFF Research Database (Denmark)

Sonne, Christian; Leifsson, Pall S.; Dietz, Rune

2006-01-01

.01) and uterine horn length and HCB (p = 0.02). The study suggests thatthere is an impact from xenoendocrine pollutants on the size of East Greenland polar bear genitalia. This may pose a riskto this polar bear subpopulation in the future because of reduced sperm and egg quality/quantity and uterus and penis size......Reproductive organs from 55 male and 44 female East Greenland polar bears were examined to investigate the potential negative impact from organohalogen pollutants (OHCs). Multiple regressions normalizing for age showed a significant inverse relationship between OHCs and testis length and baculum...... length and weight, respectively, and was found in both subadults (dichlorodiphenyl trichloroethanes, dieldrin, chlordanes, hexacyclohexanes, polychlorinated biphenyls (PCBs), and polybrominated diphenyl ethers (PBDEs)) and adults (hexachlorobenzene [HCB]) (all p

Trichloroethylene (TCE) adsorption using sustainable organic mulch

Energy Technology Data Exchange (ETDEWEB)

Wei Zongsu [Department of Civil Engineering, University of Toledo, Mail Stop 307, 3031 Nitschke Hall, 2801 W. Bancroft St., Toledo, OH, 43606-3390 (United States); Seo, Youngwoo, E-mail: youngwoo.seo@utoledo.edu [Department of Civil Engineering, University of Toledo, Mail Stop 307, 3031 Nitschke Hall, 2801 W. Bancroft St., Toledo, OH, 43606-3390 (United States)

2010-09-15

Soluble substrates (electron donors) have been commonly injected into chlorinated solvent contaminated plume to stimulate reductive dechlorination. Recently, different types of organic mulches with economic advantages and sustainable benefits have received much attention as new supporting materials that can provide long term sources of electron donors for chlorinated solvent bioremediation in engineered biowall systems. However, sorption capacities of organic mulches for chlorinated solvents have not been studied yet. In this study, the physiochemical properties of organic mulches (pine, hardwood and cypress mulches) were measured and their adsorption capacity as a potential media was elucidated. Single, binary and quaternary isotherm tests were conducted with trichloroethylene (TCE), tetrachloroethylene (PCE), trans-dichloroethylene (trans-DCE) and cis-dichloroethylene (cis-DCE). Among the three tested mulches, pine mulch showed the highest sorption capacity for the majority of the tested chemicals in single isotherm test. In binary or quaternary isotherm tests, competition among chemicals appears to diminish the differences in Q{sub e} for tested mulches. However, pine mulch also showed higher adsorption capacity for most chemicals when compared to hardwood and cypress mulches in the two isotherm tests. Based upon physicochemical properties of the three mulches, higher sorption capacity of pine mulch over hardwood and cypress mulches appears to be attributed to a higher organic carbon content and the lower polarity.

Summary and findings: Chapter A

Science.gov (United States)

Maslia, Morris L.; Suárez-Soto, René J.; Sautner, Jason B.; Anderson, Barbara A.; Jones, L. Elliott; Faye, Robert E.; Aral, Mustafa M.; Guan, Jiabao; Jang, Wonyong; Telci, Ilker T.; Grayman, Walter M.; Bove, Frank J.; Ruckart, Perri Z.; Moore, Susan M.

2013-01-01

The Agency for Toxic Substances and Disease Registry (ATSDR) is conducting epidemiological studies to evaluate the potential for health effects from exposures to volatile organic compounds (VOCs) in finished water supplied to family housing units at U.S. Marine Corps Base Camp Lejeune, North Carolina (USMCB Camp Lejeune). The core period of interest for the epidemiological studies is 1968– 1985. VOCs of major interest to the epidemiological studies include tetrachloroethylene (PCE), trichloroethylene (TCE), trans-1,2-dichloroethylene (1,2-tDCE), vinyl chloride (VC), and benzene.

Resonant inelastic x-ray scattering on iso-C2H2Cl2 around the chlorine K-edge: Structural and dynamical aspects

International Nuclear Information System (INIS)

Kawerk, Elie; Carniato, Stéphane; Journel, Loïc; Marchenko, Tatiana; Simon, Marc; Piancastelli, Maria Novella; Žitnik, Matjaž; Bučar, Klemen; Bohnic, Rok

2014-01-01

We report a theoretical and experimental study of the high resolution resonant K 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 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

Resonant inelastic x-ray scattering on iso-C2H2Cl2 around the chlorine K-edge: Structural and dynamical aspects

Science.gov (United States)

Kawerk, Elie; Carniato, Stéphane; Journel, Loïc; Marchenko, Tatiana; Piancastelli, Maria Novella; Žitnik, Matjaž; Bučar, Klemen; Bohnic, Rok; Kavčič, Matjaž; Céolin, Denis; Khoury, Antonio; Simon, Marc

2014-10-01

We report a theoretical and experimental study of the high resolution resonant Kα 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 Kα 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.

Resonant inelastic x-ray scattering on iso-C₂H₂Cl₂ around the chlorine K-edge: structural and dynamical aspects.

Science.gov (United States)

Kawerk, Elie; Carniato, Stéphane; Journel, Loïc; Marchenko, Tatiana; Piancastelli, Maria Novella; Žitnik, Matjaž; Bučar, Klemen; Bohnic, Rok; Kavčič, Matjaž; Céolin, Denis; Khoury, Antonio; Simon, Marc

2014-10-14

We report a theoretical and experimental study of the high resolution resonant K(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(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.

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

Energy Technology Data Exchange (ETDEWEB)

Kawerk, Elie, E-mail: eliekawerk@hotmail.com, E-mail: ekawerk@units.it [CNRS, UMR 7614, Laboratoire de Chimie Physique-Matière et Rayonnement, F-75005 Paris (France); Sorbonne Universités, UPMC Université Paris 06, UMR 7614, Laboratoire de Chimie Physique-Matière et Rayonnement, F-75005 Paris (France); Laboratoire de Physique Appliquée, Faculté des Sciences II, Université Libanaise, 90656 Jdeidet el Metn, Liban (Libya); Dipartimento di Scienze Chimiche, Università di Trieste, Via L. Giorgieri 1, I-34127 Trieste (Italy); Carniato, Stéphane; Journel, Loïc; Marchenko, Tatiana; Simon, Marc [CNRS, UMR 7614, Laboratoire de Chimie Physique-Matière et Rayonnement, F-75005 Paris (France); Sorbonne Universités, UPMC Université Paris 06, UMR 7614, Laboratoire de Chimie Physique-Matière et Rayonnement, F-75005 Paris (France); Piancastelli, Maria Novella [CNRS, UMR 7614, Laboratoire de Chimie Physique-Matière et Rayonnement, F-75005 Paris (France); Sorbonne Universités, UPMC Université Paris 06, UMR 7614, Laboratoire de Chimie Physique-Matière et Rayonnement, F-75005 Paris (France); Department of Physics and Astronomy, Uppsala University, P.O. Box 516, SE-751 20 Uppsala (Sweden); Žitnik, Matjaž; Bučar, Klemen; Bohnic, Rok [Jožef Stefan Institute, Jamova cesta 39, SI-1000 Ljubljana (Slovenia); 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.

Formation of glutathione conjugates by reactive metabolites of vinylidene chloride in microsomes and isolated hepatocytes

International Nuclear Information System (INIS)

Liebler, D.C.; Meredith, M.J.; Guengerich, F.P.

1985-01-01

Oxidation of the vinyl halide carcinogen and hepatotoxin vinylidene chloride (VDC) by microsomal cytochrome P-450 yields 2,2-dichloroacetaldehyde, 2-chloroacetyl chloride, 2-chloroacetic acid, and 1,1-dichloroethylene oxide. The roles of these metabolites in covalent modification of proteins and reduced glutathione (GSH) were examined. 2-Chloroacetyl chloride reacted with model thiols at least 10(3)-fold faster than did 1,1-dichloroethylene oxide and at least 10(5)-fold faster than did 2,2-dichloroacetaldehyde or 2-chloroacetic acid. Microsomal covalent binding of [ 14 C]VDC was inhibited by GSH but not by lysine, suggesting that protein thiols, rather than amino groups, are major targets. Liver microsomes catalyzed the formation of three GSH:VDC metabolite conjugates, identified as S-(2,2-dichloro-1-hydroxy)ethylglutathione, 2-(S-glutathionyl)acetate, and S-(2-glutathionyl)acetylglutathione, a novel conjugate containing both stable (thioether) and labile (thioester) linkages. The latter two conjugates also were formed in isolated rat hepatocytes and measurable amounts of 2-(S-glutathionyl)acetate were released into the incubation medium. Both 2-(S-glutathionyl)acetate and S-(2-glutathionyl)acetylglutathione were formed with [ 35 S]GSH added to the hepatic medium, indicating that reactive VDC metabolites are capable of crossing the plasma membrane to react with extracellular targets. Unlabeled S-(2-glutathionyl)-acetylglutathione underwent carbonyl substitution with added [ 35 S]GSH, suggesting that this conjugate may participate in modification of protein thiols. This conjugate also underwent hydrolysis with a half-life of approximately 3 hr. GSH:VDC metabolite conjugates may serve as accessible models for labile covalent adducts formed between VDC metabolites and protein thiols

Relação entre a freqüência de consumo de carne e pescado e os níveis de hexaclorobenzeno, lindano, aldrin e 4,4' - diclorodifenil - 1,1' dicloroetileno, em tecido adiposo de glândulas mamárias de mulheres espanholas Relationship between the frequency of meat and fish intake and the levels of hexaclorobenzene, lindane, aldrin e 4,4' dichloro diphenil 1,1' dichloroethylene, present in mamary adipose tissue samples from spanish women

Directory of Open Access Journals (Sweden)

Ijoni Costabeber

2003-02-01

Full Text Available Níveis de resíduos dos pesticidas organoclorados, hexaclorobenzeno (HCB, lindano gama-HCH, aldrin e 4,4'-diclorodifenil-1,1'dicloroetileno (p,p'-DDE foram determinados em tecido adiposo mamário de mulheres residentes em Córdoba, Espanha. A maior concentração média foi detectada para o p,p'-DDE (1,869 mig/g de tecido adiposo, que estava presente em 100% das amostras. As concentrações médias de HCB, gama-HCH e aldrin encontrados foram 0,236, 0,003 e 0,006mig/g de tecido adiposo, respectivamente. Os níveis dos resíduos detectados nas amostras foram relacionados ao consumo semanal de carne e pescado pelas doadoras. O único composto cujos níveis variaram significativamente (p£0,05 em função da freqüência de consumo de carne foi o p,p'-DDE, tendo apresentado concentração média de 2,833 mig/g de tecido adiposo quando as doadoras relataram uma freqüência de consumo de carne superior a quatro vezes por semana.The levels of organochlorine pesticide residues ¾ hexaclorobenzene (HCB, lindane (gamma-HCH, aldrin and 4,4'dichloro diphenil 1,1'dichloroethylene (p,p'-DDE - present in mammary adipose tissue samples from women living in Cordoba (Spain were evaluated. The compound found at the highest concentration was p,p´-DDE (1.869(mug/g of adipose tissue, which was present in 100% of the analyzed samples. The average levels of HCB, gamma-HCH and aldrin were 0.236, 0.003 and 0.006mug/g of adipose tissue, respectively. The tissue levels of organochlorine residues were correlated with the weekly intake of meat and fish by donors. Only the tissue levels of p-p´-DDE were significantly (p£0.05 affected by the frequency of meat intake. Donors with a meat intake higher than four times a week presented an average level of 2.833mug/g of adipose tissue.

The study of DDT in contaminated soil of abandoned DDT factory area of Amangarh Khyber Pakhtunkhwa

International Nuclear Information System (INIS)

Sanaullah, M.A.; Sabir, M.A.; Arfan, M.

2011-01-01

Dichlorodiphenyl trichloroethane (DDT) is an organo chlorine insecticide mainly used to control mosquito borne diseases and agricultural pests worldwide, including Pakistan. For DDT production a factory was established in 1963 in Amangargh, Nowshehra, KP. Although DDT production and its applications in agriculture have been banned since long and as a result the mentioned factory has also abandoned yet there remains extensive amount of DDT and contaminated sites are still releasing DDT to the environment. As a matter of fact even small amounts of DDT can affect a variety of organisms like small microorganisms, algae and plankton. DDT also causes many problems in fish, birds, mammals and somehow Human Beings. This research examined the soil's DDT concentration and its transformation at various depths of study site. The DDT from each soil sample was extracted using simply solvent extraction method. The residual DDT level found in almost all the soil samples taken was greater than the standard limit (< 17 mgKg/sup -1/). (author)

Ion channels: molecular targets of neuroactive insecticides.

Science.gov (United States)

Raymond-Delpech, Valérie; Matsuda, Kazuhiko; Sattelle, Benedict M; Rauh, James J; Sattelle, David B

2005-11-01

Many of the insecticides in current use act on molecular targets in the insect nervous system. Recently, our understanding of these targets has improved as a result of the complete sequencing of an insect genome, i.e., Drosophila melanogaster. Here we examine the recent work, drawing on genetics, genomics and physiology, which has provided evidence that specific receptors and ion channels are targeted by distinct chemical classes of insect control agents. The examples discussed include, sodium channels (pyrethroids, p,p'-dichlorodiphenyl-trichloroethane (DDT), dihydropyrazoles and oxadiazines); nicotinic acetylcholine receptors (cartap, spinosad, imidacloprid and related nitromethylenes/nitroguanidines); gamma-aminobutyric acid (GABA) receptors (cyclodienes, gamma-BHC and fipronil) and L-glutamate receptors (avermectins). Finally, we have examined the molecular basis of resistance to these molecules, which in some cases involves mutations in the molecular target, and we also consider the future impact of molecular genetic technologies in our understanding of the actions of neuroactive insecticides.

Preliminary technology report for Southern Sector bioremediation

International Nuclear Information System (INIS)

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

1997-01-01

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

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

Energy Technology Data Exchange (ETDEWEB)

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.

Health assessment for Smith's Farm, Shepherdsville, Bullitt County, Kentucky, Region 4. CERCLIS No. KYD097267413. Preliminary report

Energy Technology Data Exchange (ETDEWEB)

1988-11-15

The Smith's Farm site is on the National Priorities List. The environmental contamination on-site consists of ethylbenzene, bis-(2-ethylhexyl)phthalate, toluene, xylene, polychlorinated biphenyls, arsenic, chromium, lead, and nickel in soil; ethylbenzene, arsenic, mercury, nickel, cadmium, and zinc in surface water; ethylbenzene, toluene, bis-(2-ethylhexyl)phthalate, polychlorinated biphenyls, arsenic, chromium, lead, and nickel in sediment; and 1,1,1-trichlorethane, vinyl chloride, isophorone, benzene, trans-1,2-dichloroethylene, trichloroethylene, xylenes, arsenic, nickel, and lead in leachate. Based on the available information, 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.

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

Energy Technology Data Exchange (ETDEWEB)

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.

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

Energy Technology Data Exchange (ETDEWEB)

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.

Mixed waste management facility groundwater monitoring report. Fourth quarter 1996 and 1996 summary

International Nuclear Information System (INIS)

1997-03-01

During fourth quarter 1996, nine constituents exceeded final Primary Drinking Water Standards (PDWS) in groundwater samples from downgradient monitoring wells at the Mixed Waste Management Facility. No constituents exceeded final PDWS in samples from the upgradient monitoring wells. As in previous quarters, tritium and trichloroethylene were the most widespread elevated constituents. Carbon tetrachloride, chloroethene, chloroform, 1,1-dichloroethylene, dichloromethane, gross alpha, and tetrachloroethylene also exceeded final PDWS in one or more wells. Elevated constituents were found in numerous Aquifer Zone llB2 (Water Table) and Aquifer Zone llB1 (Barnwell/McBean) wells and in six Aquifer Unit IIA (Congaree) wells. The groundwater flow directions and rates in the three hydrostratigraphic units were similar to those of previous quarters

Mixed Waste Management Facility (MWMF) groundwater monitoring report

International Nuclear Information System (INIS)

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 2 (Water Table) and Aquifer Zone IIB 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

Health assessment for Shpack Landfill, Attleboro/North, Massachusetts, Region 1. CERCLIS No. MAD980503973. Preliminary report

International Nuclear Information System (INIS)

1989-01-01

The Shpack Landfill site is on the National Priorities List (NPL). The landfill received both domestic and industrial waste, including inorganic and organic chemicals as well as radioactive waste. Ground water contains vinyl chloride, trichloroethylene, trans-1,2-dichloroethylene, tetrachloroethylene, chromium, barium, copper, nickel, manganese, arsenic, cadmium, lead, polychlorinated biphenyl-1260 (Aroclor-1260), radium-226, alpha particles and beta particles. Surface and subsurface soil samples contained radium-226, uranium-238, uranium-235, uranium-234, and visual evidence of metal plating waste sludges. The site is considered to be of potential health concern because of the risk to human health caused by the potential for exposure to hazardous substances via ingestion of contaminated soils at the site and future ingestion of contaminated domestic well water

Removal of chlorinated organic compounds from gas phase using electron beam technology

Energy Technology Data Exchange (ETDEWEB)

Sun, Y.; Bulka, S.; Zimek, A. [Institute of Nuclear Chemistry and Technology, Warsaw (Poland); Chmielewski, A. G. [Institute of Nuclear Chemistry and Technology, Warsaw (Poland); Faculty of Chemical and Process Engineering, Warsaw University of Technology, Warsaw (Poland)

2011-07-01

Selected chlorinated organic compounds (Cl-HC), which are emitted from coal fired power plants, waste incinerators, chemical industry etc., are very harmful to the environment and human’s health. Some of them are listed as carcinogenic compounds by USA EPA. Recent studies show that some chlorinated organic compounds are suspected to be precursors for dioxins formation. Chlorinated organic compounds decomposition in air in an electron beam (EB) generated plasma reactor technology was studied. We selected cis-dichloroethylene (cis-DCE), 1,4-dichlorobenznene(1,4-DCB), 1-chloronaphthalene as studied objects. It is found that chlorinated organic compounds can be decomposed in an electron beam generated plasma reactor. The order of decomposition efficiency of these compounds are: cis-DCE > 1,4-DCB> 1-chloronaphthalene. (author)

Application of factorial design for the ab initio study of cis- and trans-1,2 dihaloethylene stabilities

Directory of Open Access Journals (Sweden)

Silva João Bosco P. da

2000-01-01

Full Text Available The chemometric technique Two Level Factorial Design was used to evaluate the principal and interaction effects of wave function modifications on calculated energy differences (DE between the cis and trans isomers of 1,2-dihaloethylenes, C2H2X2 (X=F and Cl. The factorial profile of DE is quite different for these systems. The addition of polarization and diffuse functions to the basis set have the largest effects in describing cis 1,2-difluoroethylene as the most stable isomer. In contrast electronic correlation, at the MP2 level, and the inclusion of polarization functions in the basis set have the largest effects in describing the cis form as the most stable one in the 1,2-dichloroethylenes. In both systems the interaction effects are smaller than the principal effects.

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

Energy Technology Data Exchange (ETDEWEB)

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.

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

Science.gov (United States)

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.

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

International Nuclear Information System (INIS)

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

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

International Nuclear Information System (INIS)

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

Radiation- and photoinduced degradation of pollutants in water. A comparative study

International Nuclear Information System (INIS)

Getoff, N.

1991-01-01

Absorption spectra and kinetics of the C radical 3 H 7 , n-C radical 4 H 9 , C 3 H 7 O radical 2 and n-C 4 H 9 O radical 2 transients are presented. Comparative studies on CH 2 Cl 2 , trans-1,2-dichloroethylene, trichloroethylene and tetra-chloroethylene in neutral aqueous solution with respect to their degradation under the influence of γ-rays and v.u.v.-light were performed. Based on the quantum energy (E = 6.71 eV hv for 184.9 nm) a ''photochemical'' G-value for Cl - was obtained which is about one order of magnitude higher than that resulting from γ-irradiation. This effect is based on the specific v.u.v.-light absorption by the substrates in addition to the photolysis of water. Probable reaction mechanisms for the radiation and photoinduced decomposition of the chlorinated hydrocarbons are presented. (author)

Organohalogen contamination in passerine birds from three metropolises in China: Geographical variation and its implication for anthropogenic effects on urban environments

International Nuclear Information System (INIS)

Yu, Le-Huan; Luo, Xiao-Jun; Liu, Hong-Ying; Zeng, Yan-Hong; Zheng, Xiao-Bo; Wu, Jiang-Ping; Yu, Yun-Jiang; Mai, Bi-Xian

2014-01-01

Contamination of organohalogen pollutants (OHPs), including dichlorodiphenyl trichloroethane and its metabolites (DDTs), polychlorinated biphenyls (PCBs), polybrominated diphenyl ethers (PBDEs), decabromodiphenylethane (DBDPE), hexabromocyclododecanes (HBCDs), and dechlorane plus (DP) in three metropolises of China, Beijing, Wuhan, and Guangzhou, and a reference rural site were determined using terrestrial residential passerine species as bioindicator. DDTs dominated in Wuhan whereas flame retardants dominated in Guangzhou and Beijing. No geographical variation was found for PCB levels but it exhibited different homologue profiles among different sites which could be attributed to different dietary sources of birds. Industry characteristics of the sampling location contributed to the geographical differences in the occurrence and contamination profile of OHPs. The transformation of traditional agriculture characterized contamination profiles to industry characterized profiles in Beijing and Guangzhou implicates significantly environmental concern on the flame retardants contamination in non-hot-spot regions of China. - Highlights: • Various OHPs were determined in passerine birds from three metropolises of China. • Geographical variations of OHPs levels and contamination profiles were observed. • More concern should be taken on the dominance of FRs in Chinese developed cities. • Diet source characterized by δ 13 C plays a key role in PCB pattern determination. - Geographical variations of OHPs contamination profiles indicate significant impact of industrialization and urbanization on Chinese urban environment

Purification of waters and elimination of organochloric insecticides by means of active coal

Directory of Open Access Journals (Sweden)

DRAGAN MARINOVIĆ

2010-04-01

Full Text Available Pollution of water and the determination of the degree of its pollution with numerous physical, chemical and biological polluters have become general, ever increasing social and health related problems. Within this study, the concentrations of some most frequently used organochloric insecticides (OCI: a-hexachlorocyclohexane (a-HCH, γ-hexachlorocyclohexane (lindane, heptachlor, aldrin, dieldrin, endrin, dichlorodiphenyl trichlorethane (DDT were investigated. OCI are highly toxic substances for the human population and their effective elimination from the environment is of paramount interest. To determine the OCI concentration in water samples, the EPA–608 method and the liquid–liquid extraction principle were applied. A procedure for OCI elimination was realized by passing the water over four columns filled with various active coals: KRF, K-81/B, NORIT ROW-0.8 and AQUA SORB CS. These active coals are carbonized coconut shells activated by different procedures. The obtained results indicated that best purification of potable and waste water achieved using a column with Norit Row-0.8 filling. Research proved that small quantities of OCI can also be effectively removed using a Norit Row-0.8 active coal filled column, without altering the organoleptic properties of the water, which meets the requirements of water purification processes.

Exposure to CB-153 and p,p'-DDE and human sperm chromatin integrity

Energy Technology Data Exchange (ETDEWEB)

Rignell-Hydbom, A; Rylander, L; Joensson, B A.G.; Hagmar, L [Dept. of Occupational and Environmental Medicine, Lund Univ. Hospital (Sweden); Giwercman, A [Fertility Centre, Malmoe Univ. hospital (Sweden); Spano, M [Section of Toxicology and Biomedical Sciences, ENEA Casaccia Research Centre, Rome (Italy)

2004-09-15

In Sweden, the consumption of fatty fish from the Baltic Sea (off the Swedish east coast) is the single most important source of exposure to persistent organochlorine pollutants (POPs). Fishermen from the east coast have averagely higher plasma levels of polychlorinated biphenyls (PCBs) and total POP derived TEQ in plasma than both west coast fishermen and men from the general population. Dichlorodiphenyl dichloroethene (p,p'-DDE), a relevant biomarker for POP is still present in relatively high serum concentrations in men consuming fish from the Baltic Sea. Several studies have shown that POPs are capable of interfering with reproductive and endocrine function in animals. Human studies have shown that exposure to PCBs and polychlorinated dibenzofurans (PCDFs) has a negative effect on male reproductive function, and especially sperm motility seems vulnerable. However, studies relating to human sperm genetic integrity are few. The aim of the study was to investigate whether exposure to POP using 2,2',4,4',5,5'- hexachlorobiphenyl (CB-153) and p,p'-DDE as biomarkers, are associated with sperm chromatin integrity. In order to ensure a sufficient variation in POP exposure fishermen from both the Swedish east (''more exposed'') and west coasts (''less exposed'') formed the study base.

Exposure to CB-153 and p,p'-DDE and human sperm chromatin integrity

Energy Technology Data Exchange (ETDEWEB)

Rignell-Hydbom, A.; Rylander, L.; Joensson, B.A.G.; Hagmar, L. [Dept. of Occupational and Environmental Medicine, Lund Univ. Hospital (Sweden); Giwercman, A. [Fertility Centre, Malmoe Univ. hospital (Sweden); Spano, M. [Section of Toxicology and Biomedical Sciences, ENEA Casaccia Research Centre, Rome (Italy)

2004-09-15

In Sweden, the consumption of fatty fish from the Baltic Sea (off the Swedish east coast) is the single most important source of exposure to persistent organochlorine pollutants (POPs). Fishermen from the east coast have averagely higher plasma levels of polychlorinated biphenyls (PCBs) and total POP derived TEQ in plasma than both west coast fishermen and men from the general population. Dichlorodiphenyl dichloroethene (p,p'-DDE), a relevant biomarker for POP is still present in relatively high serum concentrations in men consuming fish from the Baltic Sea. Several studies have shown that POPs are capable of interfering with reproductive and endocrine function in animals. Human studies have shown that exposure to PCBs and polychlorinated dibenzofurans (PCDFs) has a negative effect on male reproductive function, and especially sperm motility seems vulnerable. However, studies relating to human sperm genetic integrity are few. The aim of the study was to investigate whether exposure to POP using 2,2',4,4',5,5'- hexachlorobiphenyl (CB-153) and p,p'-DDE as biomarkers, are associated with sperm chromatin integrity. In order to ensure a sufficient variation in POP exposure fishermen from both the Swedish east (''more exposed'') and west coasts (''less exposed'') formed the study base.

Experimental design for assessment of electrokinetically enhanced delivery of lactate and bacteria in 1,2-cis-dichloroethylene contaminated limestone

DEFF Research Database (Denmark)

Hyldegaard, Bente Højlund; Nedergaard, L. W.; Ottosen, Lisbeth

2015-01-01

Bacterial dechlorination of chlorinated solvents often causes accumulation of the intermediate cis-DCE. Back diffusion of e.g. cis-DCE, due to the dual porosity of limestone, often limits the remediation efficiency. A remediation scheme capable of establishing contact between contaminant, degrading...... bacteria and electron donor within the low permeable limestone matrix is required. The technology EK-BIO, which combines enhanced reductive dechlorination and electrokinetics (EK), was assessed. This novel technology has not previously been tested in limestone. An experimental set-up was designed to meet...... that fermentative bacteria were distributed by electrophoresis. This study suggests that EK application can establish the essential contact and overcome back diffusion. Thereby, EK-BIO may be superior to advection-based technologies for bioremediation of chlorinated solvent contaminated limestone matrices....

Evaluation of Chlorinated Hydrocarbon Concentrations in Tehran’s Districts Drinking Water

Directory of Open Access Journals (Sweden)

Alireza Pardakhti

2012-01-01

Full Text Available In this study Tehran’s drinking water was evaluated for the presence of chlorinated hydrocarbons during spring and summer of 2009. Chlorinated hydrocarbons are an important class of environmental pollutants that cause adverse health effects on human’s kidney, liver and central nervous systems. In this study six water districts were selected for taking drinking water samples in the city of Tehran as well as one location outside the city limits. The samples were analyzed by GC/MS using EPA method 8260. The average concentrations of 1,1-dichloroethylene, 1,2 Dichloromethane, Tetra chloromethane, Trichloroethylene and tetra chloroethylene were determined during a 7 month period and the results were 0.04ppb, 0.52ppb, 0.01ppb, 0.24ppb, 0.03ppb respectively. The highest concentration of chlorinated hydrocarbon observed in Tehran’s drinking water was Trichloroethylene and the lowest concentration was Tetra chloromethane. Districts 5 and 6 showed the highest concentrations of chlorinated hydrocarbons in the city of Tehran.

Abiotic and biotic transformations of 1,1,1-trichloroethane under methanogenic conditions

International Nuclear Information System (INIS)

Vogel, T.M.; McCarty, P.L.

1987-01-01

A common industrial solvent, 1,1,1-trichloroethane (TCA), is one of the most frequently found contaminants in ground water. The fate of TCA in ground water is complicated by the different possible abiotic and biotic transformations that it may undergo. Abiotic transformation of TCA can result in a mixture of 1,1-dichloro-ethylene (1,1-DCE) and acetic acid, as shown by others. This study confirms that TCA can be biotransformed by reductive dehalogenation to 1,1-dichloroethane (1,1-DCA) and chloroethane (CA) under methanogenic conditions. Also, reductive dehalogenation of 1,1-DCE to vinyl chloride (VC) is confirmed. This study demonstrates that these transformations can occur stoichiometrically. In addition, [ 14 C]TCA, [ 14 C]-1,1-DCA, [ 14 C]-1,1-DCE, [ 14 C]CA, and [ 14 C]VC were at least partially mineralized to 14 CO 2 under similar methanogenic conditions.23 references, 3 figures, 4 tables

Time-resolved FTIR [Fourier transform infrared] emission studies of laser photofragmentation and chain reactions

International Nuclear Information System (INIS)

Leone, S.R.

1990-01-01

Recent progress is described resulting from the past three years of DOE support for studies of combustion-related photofragmentation dynamics, energy transfer, and reaction processes using a time-resolved Fourier transform infrared (FTIR) emission technique. The FTIR is coupled to a high repetition rate excimer laser which produces radicals by photolysis to obtain novel, high resolution measurements on vibrational and rotational state dynamics. The results are important for the study of numerous radical species relevant to combustion processes. The method has been applied to the detailed study of photofragmentation dynamics in systems such as acetylene, which produces C 2 H; chlorofluoroethylene to study the HF product channel; vinyl chloride and dichloroethylene, which produce HCl; acetone, which produces CO and CH 3 ; and ammonia, which produces NH 2 . In addition, we have recently demonstrated use of the FTIR technique for preliminary studies of energy transfer events under near single collision conditions, radical-radical reactions, and laser-initiated chain reaction processes

Mixed Waste Management Facility groundwater monitoring report: Third quarter 1994

International Nuclear Information System (INIS)

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

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

Energy Technology Data Exchange (ETDEWEB)

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

Chemical aspects of the radioactive decay 38S to 38Cl

International Nuclear Information System (INIS)

Leurs, C.J.

1978-01-01

The cyclotron-production of 38 S with the reaction 40 Ar(p,3p) 38 S is described. An excitation curve for this nuclear reaction is given and the chemistry used to produce sulfates labeled with 38 S and H 2 38 S is described. The probability distribution of the recoil energy of 38 Cl, produced by beta-decay of 38 S, is given. The probability for rupture of the original bonds due to the radioactive decay process, is estimated for gaseous H 2 38 S and for crystalline sulfates- 38 S. The results are given for the β,γ-decay of 38 S to 38 Cl under different circumstances in inorganic solid sulfates (with and without water of crystallization) and in the mixed crystal K 2 SO 4 .K 2 BeF 4 (1 : 2500). Finally, the reactions of 38 Cl, produced by radioactive decay of 38 S (as H 2 38 S) with gaseous 1,2-dichloroethylene are discussed

Stable carbon isotope fractionation of chlorinated ethenes by a microbial consortium containing multiple dechlorinating genes.

Science.gov (United States)

Liu, Na; Ding, Longzhen; Li, Haijun; Zhang, Pengpeng; Zheng, Jixing; Weng, Chih-Huang

2018-08-01

The study aimed to determine the possible contribution of specific growth conditions and community structures to variable carbon enrichment factors (Ɛ- carbon ) values for the degradation of chlorinated ethenes (CEs) by a bacterial consortium with multiple dechlorinating genes. Ɛ- carbon values for trichloroethylene, cis-1,2-dichloroethylene, and vinyl chloride were -7.24% ± 0.59%, -14.6% ± 1.71%, and -21.1% ± 1.14%, respectively, during their degradation by a microbial consortium containing multiple dechlorinating genes including tceA and vcrA. The Ɛ- carbon values of all CEs were not greatly affected by changes in growth conditions and community structures, which directly or indirectly affected reductive dechlorination of CEs by this consortium. Stability analysis provided evidence that the presence of multiple dechlorinating genes within a microbial consortium had little effect on carbon isotope fractionation, as long as the genes have definite, non-overlapping functions. Copyright © 2018 Elsevier Ltd. All rights reserved.

Determination of extractable organohalogens in apple by neutron activation analysis and gas chromatography

International Nuclear Information System (INIS)

Zhang, H.; Chai, Z.F.; Sun, H.B.; Zhang, J.L.; Sun, J.Q.

2005-01-01

In addition to compounds such as dichlorodiphenyl trichloroethanes (DDTs) and polychlorinated biphenyls (PCBs), which originate from by now well-known anthropogenic sources, there is increasing awareness of other halogenated compounds coming from a number of different processes, and probably also from natural source. To provide the reliable results and data for evaluation of hazard of extractable persistent organohalogen (EPOX) to food safety and to further characterize halogenated compounds in fruits, the concentrations of extractable organohalogen (EOX), EPOX, and identified organochlorine compounds including DDTs, hexachlorinated cyclohexanes (HCHs), chlordanes and PCBs in apple samples from Chinese homegrown and imports were determined by neutron activation analysis (NAA) and gas chromatography. The results indicated that the levels of EPOX in apples was in the order of EPOCl >> EPOBr > EPOI, which showed that EPOCl was the major fraction of the EPOX pollutions. Also, most chlorinated compounds in apple samples existed as inorganic species and water-soluble polar compounds, and about 1/10-4/5 of EOX was sulfuric acid-resistant EPOX contaminants. Meanwhile, about more than 94 % of EPOCl in detected specimens cannot be accounted for by DDTs, HCHs, chlordanes and PCBs. Furthermore, the T-test result indicated that the EPOCl levels in apple were significantly higher than those in peeled apple , which stated that people consuming peeled apple will get lesser intakes of EPOCl pollutants than they consume unpeeled apple.

Thermal and Dielectric Behavior Studies of Poly(Arylene Ether Sulfones with Sulfonated and Phosphonated Pendants

Directory of Open Access Journals (Sweden)

Shimoga D. Ganesh

2016-01-01

Full Text Available The present paper discusses the aspects of the synthesizing valeric acid based poly(ether sulfones with active carboxylic acid pendants (VALPSU from solution polymerization technique via nucleophilic displacement polycondensation reaction among 4,4′-dichlorodiphenyl sulfone (DCDPS and 4,4′-bis(4-hydroxyphenyl valeric acid (BHPA. The conditions necessary to synthesize and purify the polymer were investigated in some detail. The synthesized poly(ether sulfones comprise sulfone and ether linkages in addition to reactive carboxylic acid functionality; these active carboxylic acid functional groups were exploited to hold the phenyl sulphonic acid and phenyl phosphonic acid pendants. The phenyl sulphonic acid pendants in VALPSU were easily constructed by altering active carboxylic acid moieties by sulfanilic acid using N,N′-dicyclohexylcarbodiimide (DCC mediated mild synthetic route, whereas the latter one was built in two steps. Initially, polyphosphoric acid condensation with VALPSU by 4-bromoaniline and next straightforward palladium catalyzed synthetic route, in both of which acidic pendants are clenched by polymer backbone via amide linkage. Without impairing the primary polymeric backbone modified polymers were prepared by varying the stoichiometric ratios of respective combinations. All the polymers were physicochemically characterized and pressed into tablets; electrical contacts were established to study the dielectric properties. Finally, the influence of the acidic pendants on the dielectric properties was examined.

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

International Nuclear Information System (INIS)

Kelsey, Jason W.; White, Jason C.

2005-01-01

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. - Interactions between earthworms and plants affect both the phytoextraction and bioaccumulation of p,p'-DDE in soil

Effect of toluene concentration and hydrogen peroxide on Pseudomonas plecoglossicida cometabolizing mixture of cis-DCE and TCE in soil slurry.

Science.gov (United States)

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

2015-12-01

An indigenous Pseudomonas sp., isolated from the regional contaminated soil and identified as P. plecoglossicida, was evaluated for its aerobic cometabolic removal of cis-1,2-dichloroethylene (cis-DCE) and trichloroethylene (TCE) using toluene as growth substrate in a laboratory-scale soil slurry. The aerobic simultaneous bioremoval of the cis-DCE/TCE/toluene mixture was studied under different conditions. Results showed that an increase in toluene concentration level from 300 to 900 mg/kg prolonged the lag phase for the bacterial growth, while the bioremoval extent for cis-DCE, TCE, and toluene declined as the initial toluene concentration increased. In addition, the cometabolic bioremoval of cis-DCE and TCE was inhibited by the presence of hydrogen peroxide as the additional oxygen source, while the bioremoval of toluene (900 mg/kg) was enhanced after 9 days of incubation. The subsequent addition of toluene did not improve the cometabolic bioremoval of cis-DCE and TCE. The obtained results would help to enhance the applicability of bioremediation technology to the mixed waste contaminated sites.

Decomposition of tetrachloroethylene by ionizing radiation

International Nuclear Information System (INIS)

Hakoda, T.; Hirota, K.; Hashimoto, S.

1998-01-01

Decomposition of tetrachloroethylene and other chloroethenes by ionizing radiation were examined to get information on treatment of industrial off-gas. Model gases, airs containing chloroethenes, were confined in batch reactors and irradiated with electron beam and gamma ray. The G-values of decomposition were larger in the order of tetrachloro- > trichloro- > trans-dichloro- > cis-dichloro- > monochloroethylene in electron beam irradiation and tetrachloro-, trichloro-, trans-dichloro- > cis-dichloro- > monochloroethylene in gamma ray irradiation. For tetrachloro-, trichloro- and trans-dichloroethylene, G-values of decomposition in EB irradiation increased with increase of chlorine atom in a molecule, while those in gamma ray irradiation were almost kept constant. The G-value of decomposition for tetrachloroethylene in EB irradiation was the largest of those for all chloroethenes. In order to examine the effect of the initial concentration on G-value of decomposition, airs containing 300 to 1,800 ppm of tetrachloroethylene were irradiated with electron beam and gamma ray. The G-values of decomposition in both irradiation increased with the initial concentration. Those in electron beam irradiation were two times larger than those in gamma ray irradiation

Preliminary assessment of laboratory techniques for measurement of volatiles through soils at hazardous waste sites

International Nuclear Information System (INIS)

Breckenridge, R.P.; Case, J.T.

1985-01-01

This study was conducted to determine if an inexpensive laboratory screening technique could be developed to detect the presence of hazardous volatile compounds without disturbing the soil over buried waste. A laboratory investigation was designed to evaluate the movement of two volatile organics through packed soil columns. Six soil columns were filled with three different soils. Two volatile organics, trichloroethylene (TCE) and dichloroethylene (1, 2 DCE), were placed at the base of the columns as a saturated water solution. Column headspace analysis was performed by purging the top of the columns with nitrogen gas and bubbling this gas through a pentane trap. Samples in the air space were also collected using 25 and 100 microliter gas tight syringes. All samples were analyzed using Electron Capture Detector (ECD) by gas chromatography. Results indicate that the volatile organic compounds can be detected through a five foot column of soil in concentrations down to parts-per-billion (ppb) for both TCE and DCE. Distribution coefficients (Kd) experiments were also conducted to assess breakthrough time and related concentration with soil type

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

Energy Technology Data Exchange (ETDEWEB)

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.

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

International Nuclear Information System (INIS)

Chmielewski, A.G.; Sun Yongxia; Bulka, S.; Zimek, Z.

2004-01-01

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

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

International Nuclear Information System (INIS)

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

2009-01-01

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. - A chlorine balance performed on a planted test bed with PCE-contaminated water demonstrated VOC mass reduction of 99% and complete dechlorination.

Purification by bioremediation of soil and underground water contaminated by volatile organic chloride. Bioremediation gijutsu wo mochiiru kihatsusei yuki enso kagobutsu osen dojo chikasui no joka

Energy Technology Data Exchange (ETDEWEB)

Yagi, O; Uchiyama, H [National Institute for Environmental Studies, Tsukuba (Japan)

1993-08-01

Taking up a case with trichloroethylene as an example, research is introduced on the purification which is made by utilizing bioremediation technology for the contaminated soil and underground water. That technology can be said to be a method in which the contaminated environment is remedied by utilizing the biological function. First, it is necessary to separate the microorganisms which decompose the trichloroethylene. Decomposing bacteria being searched in different places, discovered was a mixed cultivation system which decomposed the trichloroethylene, if aerobic and co-existent with methane. Upon repeating the separation, a new stock was found and named Methylocystis sp. M stock. That stock proliferates by taking methane and methanol which are the sole carbon source at temperatures below 37 centigrade. That stock decomposes 1, 1-dichloroethylene and chloroform as well as the trichloroethylene, but does not tetrachloroethylene and carbon tetrachloride. That stock was studied to be fixed and used as a bioreactor. Among different fixing bacteria, alginic acid gel gave a high efficiency in decomposing the trichloroethylene. 9 refs., 5 figs., 1 tab.

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

Energy Technology Data Exchange (ETDEWEB)

Andrew James, C. [University of Washington, Department of Civil and Environmental Engineering, Seattle, WA (United States); Xin Gang [Hydranautics, 401 Jones Rd., Oceanside, CA 92058 (United States); Doty, Sharon L.; Muiznieks, Indulis [University of Washington, College of Forest Resources, Seattle, WA (United States); Newman, Lee [Brookhaven National Laboratory, Biology Department, Upton, NY (United States); Strand, Stuart E., E-mail: sstrand@u.washington.ed [University of Washington, Department of Civil and Environmental Engineering, Seattle, WA (United States)

2009-08-15

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{sup -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{sup -1}, 3.9 mg L{sup -1}, and 1.9 mg L{sup -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. - A chlorine balance performed on a planted test bed with PCE-contaminated water demonstrated VOC mass reduction of 99% and complete dechlorination.

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

Science.gov (United States)

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.

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

Science.gov (United States)

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.

Quenching of liquid scintillator fluorescence by chloroalkanes and chloroalkenes

International Nuclear Information System (INIS)

Hariharan, Chithra; Mishra, A.K.

2000-01-01

The fluorescence quenching of 2,5-diphenyloxazole (PPO) by a series of chloroalkanes and chloroalkenes including carbon tetrachloride, chloroform, dichloroethane, tetrachloroethane, dichloroethylene, trichloroethylene and tetrachloroethylene was studied in toluene as solvent at room temperature. CCl 4 was found to be the most efficient quencher in the series. The quenching was found to be appreciable and a positive deviation from linearity was observed in the Stern-Volmer (SV) plots for all the quenchers in the concentration range studied. From the studies of effect of temperature, solvent viscosity and excitation wavelength dependence for the PPO-CCl 4 system, it was inferred that non-linearity is due to the presence of a minor static quenching component in an overall dynamic quenching. The static (K S ) and the dynamic (K D ) quenching constants were calculated from the modified SV equation using quadratic least square fits. Fluorescence quenching experiments with CCl 4 were done for four other scintillators (POPOP, α-NPO, BBO and PBBO). The mechanism of quenching was established to be via charge-transfer, with the direction of transfer being from the scintillators to the chloroalkanes and chloroalkenes

Anaerobic Transformation of Chlorinated Aliphatic Hydrocarbons in a Sand Aquifer Based on Spatial Chemical Distributions

Science.gov (United States)

Semprini, Lewis; Kitanidis, Peter K.; Kampbell, Don H.; Wilson, John T.

1995-04-01

We estimated the distribution of chlorinated aliphatic hydrocarbons (CAHs) from groundwater samples collected along three transects in a sand aquifer. Trichloroethylene (TCE) leaked and contaminated the aquifer probably more than a decade before we collected the measurements. The data show significant concentrations of TCE, cis-l,2-dichloroethylene (c-DCE), vinyl chloride (VC), and ethene. We attributed DCE, VC, and ethene to the reductive dehalogenation of TCE. The CAH concentrations varied significantly with depth and correlate with sulfate and methane concentrations. Anoxic aquifer conditions exist with methane present at relatively high concentrations at depth. High concentrations of TCE correspond with the absence of methane or low methane concentrations, whereas products of TCE dehalogenation are associated with higher methane concentrations and low sulfate concentrations. Indications are that the dechlorination of TCE and DCE to VC and ethene is associated with sulfate reduction and active methanogenesis. TCE dechlorination to DCE is likely occurring under the less reducing conditions of sulfate reduction, with further reductions to VC and ethene occurring under methanogenic conditions. We estimated that about 20% of TCE has dechlorinated to ethene. The analysis of the data enhanced our knowledge of natural in situ transformation and transport processes of CAHs.

Poly-brominated diphenyl-ethers (PBDEs) and other persistent organic pollutants in blood of penguins from the Ross Sea (Antarctica)

Energy Technology Data Exchange (ETDEWEB)

Corsolini, S.; Ademollo, N.; Mariottini, M.; Focardi, S. [Universita degli Studi di Siena, Siena (Italy)

2004-09-15

Polychlorobiphenyls (PCBs), hexachlorobenzene (HCB), polybrominated diphenyl ethers (PBDEs) and dichlorodiphenyl-dichloro ethane (pp'-DDE) including its isomers and metabolites are known as POPs very well. POPs are particularly hazardous to wildlife not only because they are toxic but because they are persistent and distributed on global scale. Polybrominated diphenyl ethers (PBDEs) are a class of POPs used worldwide as flame retardants with an increasing trend in the market demand (67.4 ktons in 2001), but with some restrictions in their usage in Europe. PBDEs are hydrophobic, highly soluble in lipids, resistant to biodegradation and have similar behavior to polychlorinated biphenyls (PCBs) in aquatic and terrestrial ecosystems. Their bioaccumulation and biomagnification properties, as well their global increasing presence, have already been reported by many authors. PBDEs have been detected in remote Arctic regions10 that seem to be their final sink. PBDEs show acute toxicity and a prolonged exposure can affect the function of thyroid and cause neurodevelopmental disorders and estrogenic and hepatic effects. Furthermore, a synergic effect with dioxin-like compounds or other POPs cannot be excluded. The two aims of this study are: (1) to evaluate accumulation levels and patterns of PCBs, PBDEs and chlorinated pesticides in blood samples of the Adelie penguin, Pygoscelis adeliae, the Emperor penguin, Aptenodytes forsteri and the South Polar skua, Cataracta maccormicki from three sites in the Ross Sea (Antarctica); (2) to assess the suitability of blood for the detection of POP residues in supposedly low contaminated organisms that live in protected/ecologically sensitive areas.

Persistent organochlorine pollutants with endocrine activity and blood steroid hormone levels in middle-aged men.

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Elise Emeville

Full Text Available BACKGROUND: Studies relating long-term exposure to persistent organochlorine pollutants (POPs with endocrine activities (endocrine disrupting chemicals on circulating levels of steroid hormones have been limited to a small number of hormones and reported conflicting results. OBJECTIVE: We examined the relationship between serum concentrations of dehydroepiandrosterone, dehydroepiandrosterone sulphate, androstenedione, androstenediol, testosterone, free and bioavailable testosterone, dihydrotestosterone, estrone, estrone sulphate, estradiol, sex-hormone binding globulin, follicle-stimulating hormone, and luteinizing hormone as a function of level of exposure to three POPs known to interfere with hormone-regulated processes in different way: dichlorodiphenyl dichloroethene (DDE, polychlorinated biphenyl (PCB congener 153, and chlordecone. METHODS: We collected fasting, morning serum samples from 277 healthy, non obese, middle-aged men from the French West Indies. Steroid hormones were determined by gas chromatography-mass spectrometry, except for dehydroepiandrosterone sulphate, which was determined by immunological assay, as were the concentrations of sex-hormone binding globulin, follicle-stimulating hormone and luteinizing hormone. Associations were assessed by multiple linear regression analysis, controlling for confounding factors, in a backward elimination procedure, in multiple bootstrap samples. RESULTS: DDE exposure was negatively associated to dihydrotestosterone level and positively associated to luteinizing hormone level. PCB 153 was positively associated to androstenedione and estrone levels. No association was found for chlordecone. CONCLUSIONS: These results suggested that the endocrine response pattern, estimated by determining blood levels of steroid hormones, varies depending on the POPs studied, possibly reflecting differences in the modes of action generally attributed to these compounds. It remains to be investigated whether

Synthesis and properties of a novel sulfonated poly(arylene ether ketone sulfone) membrane with a high β-value for direct methanol fuel cell applications

International Nuclear Information System (INIS)

Xu, Jingmei; Ma, Li; Han, Hailan; Ni, Hongzhe; Wang, Zhe; Zhang, Huixuan

2014-01-01

Highlights: • Introduction of carboxyl groups into copolymers resulted in extensive hydrogen bond. • The C-SPAEKS membranes had obviously hydrophilic/hydrophobic phase separation. • The membranes showed low methanol permeability and high β values. • The membranes exhibited good thermal property and desirable mechanical performance. - Abstract: Sulfonated poly(arylene ether ketone sulfone) membranes containing carboxylic acid groups (C-SPAEKS) with different degrees of sulfonation were synthesized by the nucleophilic aromatic substitution reactions of 4-carboxylphenyl hydroquinone (4C-PH), bisphenol A, 3,3′-disulfonated 4,4′-dichlorodiphenyl sulfone, and 4,4′-difluorobenzophenone. The Fourier transform infrared and 1 H NMR analyses of C-SPAEKS revealed the presence of carboxylic acid groups in the C-SPAEKS membranes. The membranes exhibited a low swelling degree and methanol crossover level. The effects of different degrees of sulfonation on the water uptake, proton conductivity, and methanol permeability coefficient of the membranes were studied. The maximum proton conductivity of C-SPAEKS-80 membrane at room temperature was 0.069 S cm −1 , which was higher than that of Nafion ® 117 membrane. The methanol permeability coefficient of C-SPAEKS-80 membrane was 9.15 × 10 −7 cm 2 s −1 at 20 °C, much lower than that of Nafion 117 membrane (22.9 × 10 −7 cm 2 s −1 ). Furthermore, the carboxyl group-containing membranes exhibited a high β-value, further confirming that this series of membranes possess excellent comprehensive performance and can be applied in direct methanol fuel cells

Biodegradation of 1,1,1-trichloro-2,2-bis(4-chlorophenyl) ethane (DDT) by using Serratia marcescens NCIM 2919.

Science.gov (United States)

Grewal, Jasneet; Bhattacharya, Amrik; Kumar, Sumit; Singh, Dileep K; Khare, Sunil K

2016-12-01

A solvent tolerant bacterium Serratia marcescens NCIM 2919 has been evaluated for degradation of DDT (1,1,1-trichloro-2,2-bis (4-chlorophenyl) ethane). The bacterium was able to degrade up to 42% of initial 50 mg L -1 of DDT within 10 days of incubation. The highlight of the work was the elucidation of DDT degradation pathway in S. marcescens. A total of four intermediates metabolites viz. 2,2-bis (chlorophenyl)-1,1-dichloroethane (DDD), 2,2-bis (chlorophenyl)-1,1-dichloroethylene (DDE), 2,2-bis (chlorophenyl)-1-chloroethylene (DDMU), and 4-chlorobenzoic acid (4-CBA) were identified by GC-Mass and FTIR. 4-CBA was found to be the stable product of DDT degradation. Metabolites preceding 4-CBA were not toxic to strain as reveled through luxuriant growth in presence of varying concentrations of exogenous DDD and DDE. However, 4-CBA was observed to inhibit the growth of bacterium. The DDT degrading efficiency of S. marcescens NCIM 2919 hence could be used in combination with 4-CBA utilizing strains either as binary culture or consortia for mineralization of DDT. Application of S. marcescens NCIM 2919 to DDT contaminated soil, showed 74.7% reduction of initial 12.0 mg kg -1 of DDT after 18-days of treatment.

Time-resolved studies of free radicals and laser-initiated chain reactions: Final report, 1 April 1979-31 March 1988

International Nuclear Information System (INIS)

Leone, S.R.

1988-03-01

Pulsed lasers were used in this work to photofragment molecules or to initiate chain reactions. One of the major advances was the availability of high-powered rare gas halide excimer lasers. In addition, pulsed Nd:YAG lasers and dye lasers were used throughout. Results include: generalized kinetic formulations of the problem of laser-initiated chain reactions. Several studies were carried out to explore the details of chain combustion phenomena, slow chain reactions, chain branching behavior, and vibrational temperatures of combusting mixtures. A method to determine the rotational temperature of nitrogen molecules by laser multiphoton ionization was shown. The chain reaction methodology was applied to complex polyatomic systems, in which complete infrared spectra of the emitting species were obtained. Systems studied included, chlorine + HBr, HI, methane, hydrogen, ethane, propane, butane, cyclopropane, and cyclohexane. Photofragmentation studies involved the production and analysis of radical species, such as methyl, CH 2 I, and CCH. Molecules studied included methylene iodide, methyl iodide, dimethyl mercury, acetone, acetylene, vinyl chloride, dichloroethylene, and fluorochloroethylene. The first infrared characterization of a highly vibrationally excited radical was shown. Reactions of methyl radicals were studied in detail, in which a new method for obtaining absolute values of the methyl radical reaction rates were obtained

Meeting the challenge of constructing a uniquely difficult barrier wall

International Nuclear Information System (INIS)

Stamnes, R.L.; Orlean, H.M.; Thompson, N.E.

1997-01-01

A soil-bentonite vertical barrier wall with intersecting and round corners was constructed in complex geology and steep terrain to enclose and dewater a 1.4 hectare (3.5 acre) area once used for hazardous waste lagoons and landfills at the Queen City Farms (QCF) Superfund site in Maple Valley, Washington. The barrier system, including cap and barrier wall, was designed to contain light non-aqueous phase liquid (LNAPL), in addition to subsurface soil and ground water contaminated with chromium, polychlorinated biphenyls, polyaromatic hydrocarbons, trichloroethylene, dichloroethylene and vinyl chloride in the dissolved-phase. These contaminants threaten a drinking water aquifer beneath the site. Constructing the vertical barrier was a challenge due to steep slopes of 20 percent along the alignment (19.2 meter elevation change in the top of the wall), a 22.5 meter (75 foot) design wall depth, heavily consolidated clays and silts, open works gravels (gravel without finer soils), and geologic discontinuity. The barrier wall is keyed into either a glacial till or thin clayey-silt aquitard. Extensive earth moving, stepped walls and many construction techniques were used to enable construction of this barrier wall. Commonly accepted constructability criteria would have discouraged the construction of this wall

Biotransformation of chlorinated aliphatic solvents in the presence of aromatic compounds under methanogenic conditions

International Nuclear Information System (INIS)

Liang, L.N.; Grbic-Galic, D.

1993-01-01

Transformation of carbon tetrachloride (CT) and tetrachloroethylene (PCE) was studied under methanogenic conditions, in the presence or absence of toluene, ethylbenzene, phenol, and benzoate. Microbial inoculate for the experiments were derived from three groundwater aquifers contaminated by jet fuel or creosote. CT and PCE were reductively dechlorinated in all the examined castes (CT to chloroform [CF]; PCE to trichloroethylene [TCE], trans-1,2-dichloroethylene [DCE], and vinyl chloride [VC]). In the aquifer microcosms, the electron donors used for the reductive transformations were most likely the unidentified organic compounds present on aquifer solids, or storage materials in microorganisms. Alternatively, molecular hydrogen from the anaerobic incubator atmosphere could have been used. The addition of benzoate caused a decrease in rates of dechlorination if benzoate was transformed. Phenol and ethylbenzene were not degraded and did not influence the transformation of CT or PCE. Toluene, in most of the studied cases, had no influence on reductive dechlorination of either CT or PCE. Only in microcosms derived from a JP-4 jet fuel-contaminated aquifer did the anaerobic degradation of toluene occur simultaneously with reductive dechlorination of PCE, suggesting that toluene might possibly have been used as an electron donor for reductive transformation of chlorinated solvents

Bioremediation potential of toxics by manipulation of deep terrestrial subsurface ecosystems

International Nuclear Information System (INIS)

Phelps, T.J.

1990-01-01

Mixed physiological types of bacteria in consortia recovered from subsurface contaminated sediments degrade mixed organic wastes containing carbon-rich (benzene, xylene, toluene) and halogenated hydrocarbon substrates (chlorobenzene, trichloroethylene, dichloroethylenes, vinyl chloride) in column bioreactors when provided with oxygen and methane and/or propane substrates. In expanded bed bioreactors degradation proceeds to 99% completion for several organic and chlorocarbon contaminants (60% for tetrachloroethylene) to carbon dioxide on repeated cycles in 21 days with little loss of volatiles in the control bioreactor except for a 70% loss of vinyl chloride in the control. Biodegradation is most efficient when the microbial consortia is maintained in a suboptimal nutritional state which can be monitored by ratios of endogenous storage lipid (poly beta-hydroxy alkanoic acid, PHA) to total phospholipid ester-linked fatty acids (PLFA). Under the best conditions the efficiency of biodegradation was 50-65 moles substrate (propane or propane + methane)/mole of TEC degraded. The microbial communities showed a rich diversity of microbes based on PLFA biomarkers. The effects of adding methane and/or propane in inducing specific subsets of the microbial community can readily be detected in the PLFA biomarker. Despite the presence of carbon rich substrates (benzene, toluene, xylene) in the mixed wastes, no evidence of plugging of interstitial spaces by exopolysaccharide was detected

Biodegradation of chlorinated ethenes by a methane-utilizing mixed culture

International Nuclear Information System (INIS)

Fogel, M.M.; Taddeo, A.R.; Fogel, S.

1986-01-01

Chlorinated ethenes are toxic substances which are widely distributed groundwater contaminants and are persistent in the subsurface environment. Reports on the biodegradation of these compounds under anaerobic conditions which might occur naturally in groundwater show that these substances degrade very slowly, if at all. Previous attempts to degrade chlorinated ethenes aerobically have produced conflicting results. A mixed culture containing methane-utilizing bacteria was obtained by methane enrichment of a sediment sample. Biodegradation experiments carried out in sealed culture bottles with radioactively labeled trichloroethylene (TCE) showed that approximately half of the radioactive carbon had been converted to 14 CO 2 and bacterial biomass. In addition to TCE, vinyl chloride and vinylidene chloride could be degraded to products which are not volatile chlorinated substances and are therefore likely to be further degraded to CO 2 . Two other chlorinated ethenes, cis and trans-1,2-dichloroethylene, were shown to degrade to chlorinated products, which appeared to degrade further. A sixth chlorinated ethene, tetrachloroethylene, was not degraded by the methane-utilizing culture under these conditions. The biodegradation of TCE was inhibited by acetylene, a specific inhibitor of methane oxidation by methanotrophs. This observation supported the hypothesis that a methanotroph is responsible for the observed biodegradations

Advances in Biodegradation of Multiple Volatile Organic Compounds

Science.gov (United States)

Zhang, M.; Yoshikawa, M.

2017-12-01

Bioremediation of soil and groundwater containing multiple contaminants remains a challenge in environmental science and engineering because complete biodegradation of all components is necessary but very difficult to accomplish in practice. This presentation provides a brief overview on advances in biodegradation of multiple volatile organic compounds (VOCs) including chlorinated ethylenes, benzene, toluene and dichloromethane (DCM). Case studies on aerobic biodegradation of benzene, toluene and DCM, and integrated anaerobic-aerobic biodegradation of 7 contaminants, specifically, tetrachloroethylene (PCE), trichloroethylene (TCE), cis-dichloroethylene (cis-DCE), vinyl chloride (VC), DCM, benzene and toluene will be provided. Recent findings based on systematic laboratory experiments indicated that aerobic toluene degradation can be enhanced by co-existence of benzene. Propioniferax, not a known benzene, toluene and DCM degrader can be a key microorganism that involves in biodegradation when the three contaminants co-exist. Integrated anaerobic-aerobic biodegradation is capable of completely degrading the seven VOCs with initial concentrations less than 30 mg/L. Dehalococcoides sp., generally considered sensitive to oxygen, can survive aerobic conditions for at least 28 days, and can be activated during the subsequent anaerobic biodegradation. This presentation may provide a systematic information about biodegradation of multiple VOCs, and a scientific basis for the complete bioremediation of multiple contaminants in situ.

Chlorinated and Non chlorinated-Volatile Organic Compounds (Vocs) in Drinking Water of Peninsular Malaysia

International Nuclear Information System (INIS)

Mohd Pauzi Abdullah; Chian, S.S.

2011-01-01

A survey undertaken in Peninsular Malaysia has shown that volatile organic compounds (VOCs), both chlorinated and non-chlorinated, are present in selected drinking water samples. In this study, analyses of VOCs were performed by means of solid phase micro extraction (SPME) with a 100 μm polydimethylsiloxane (PDMS) fibre followed by gas chromatography - mass spectrometry detector (GC-MSD). Samples from different points of the distribution system networks were taken and analysed for 54 VOCs of different chemical families. The results of the study indicated that chloroform constituted the major portion of the VOCs in all samples analysed. In addition to trihalo methanes (THMs), other abundant compounds detected were cis and trans-1,2-dichloroethylene, trichloroethylene, 1,2-dibromoethane, benzene, toluene, ethylbenzene, chlorobenzene, 1,4-dichlorobenzene and 1,2-dichlorobenzene. However, the measured concentrations did not exceed the National Guideline for Drinking Water Quality 2000 in any case. No clear relationship between the status of development of a state in Malaysia to the levels and types of VOCs detected in its drinking water was noted. Nevertheless, the finding of anthropogenic chemicals, even at low concentrations, gave credibility to the viewpoint that improper development and disposal practices threatened the purity of the drinking water. (author)

Collisional energy dependence of molecular ionization by metastable rare gas atoms

International Nuclear Information System (INIS)

Martin, R.M.; Parr, T.P.

1979-01-01

The collisional energy dependence of several molecular total ionization cross sections by metastable rare gas atoms was studied over the thermal energy region using the crossed molecular beam time-of-flight method. Results are reported for the collision systems He, Ne, and Ar ionizing the geometric isomers cis- and trans-dichloroethylene and ortho- and para-dichlorobenzene. The He ionization cross sections oscillate about an energy dependence of E/sup -1/2/ over the energy range 0.004--1.0 eV, and the Ar*+para-dichlorobenzene cross section oscillates about an energy dependence of E/sup -2/5/ over the energy range 0.011--0.64 eV. The remaining systems are characterized by ''bent'' E/sup -m/ dependences with m values of 0.56--0.70 at low energies changing to 0.07--0.29 at higher energies. Comparison with the slopes of the He* systems and the Ar*+para-dichlorobenzene system shows that the ''bent'' and ''oscillating'' energy dependences are similar except for the form of the cross section functions at the lowest energies. No systematic differences are found between the cross section energy dependences for ionization of different geometric isomers or for ionization by the different metastable rare gas atoms

Hanford Site ground-water monitoring for 1995

International Nuclear Information System (INIS)

Dresel, P.E.; Rieger, J.T.; Webber, W.D.; Thorne, P.D.; Gillespie, B.M.; Luttrell, S.P.; Wurstner, S.K.; Liikala, T.L.

1996-08-01

This report presents the results of the Groundwater Surveillance Project monitoring for calendar year 1995 on the Hanford Site, Washington. Hanford Site operations from 1943 onward produced large quantities of radiological and chemical waste that impacted groundwater quality on the site. Monitoring of water levels and groundwater chemistry is performed to track the extent of contamination, to note trends in contaminant concentrations,a nd to identify emerging groundwater quality problems. Data from other monitoring and characterization programs were incorporated to provide an integrated assessment of onsite groundwater quality. A three- dimensional, numerical, groundwater model is being developed to improve predictions of contaminant transport. The existing two- dimensional model was applied to predict contaminant flow paths and the impact of changes on site conditions. These activities were supported by limited hydrogeologic characterization. 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. Radiological monitoring results indicated that many radioactive contaminants were above US Environmental Protection Agency or State of Washington drinking water standards at the Hanford Site. Nitrate, fluoride, chromium, cyanide, carbon tetrachloride, chloroform, trichloroethylene, and cis-1,2-dichloroethylene were present in groundwater samples at levels above their US EPA or State of Washington maximum contaminant levels

Pilot-Scale Demonstration of In-Situ Chemical Oxidation ...

Science.gov (United States)

A pilot-scale in situ chemical oxidation (ISCO) demonstration, involving subsurface injections of sodium permanganate (NaMnO4), was performed at the US Marine Corp Recruit Depot (MCRD), site 45 (Parris Island (PI), SC). The ground water was originally contaminated with perchloroethylene (PCE) (also known as tetrachloroethylene), a chlorinated solvent used in dry cleaner operations. High resolution site characterization involved multiple iterations of soil core sampling and analysis. Nested micro-wells and conventional wells were also used to sample and analyze ground water for PCE and decomposition products (i.e., trichloroethyelene (TCE), dichloroethylene (c-DCE, t-DCE), and vinyl chloride (VC)), collectively referred to as chlorinated volatile organic compounds (CVOC). This characterization methodology was used to develop and refine the conceptual site model and the ISCO design, not only by identifying CVOC contamination but also by eliminating uncontaminated portions of the aquifer from further ISCO consideration. Direct-push injection was selected as the main method of NaMnO4 delivery due to its flexibility and low initial capital cost. Site impediments to ISCO activities in the source area involved subsurface utilities, including a high pressure water main, a high voltage power line, a communication line, and sanitary and stormwater sewer lines. Utility markings were used in conjunction with careful planning and judicious selection of injection locations. A

Inorganic photocatalytic membranes for the remediation of VOCs in groundwater at the Portsmouth Site

International Nuclear Information System (INIS)

Bischoff, B.L.; Fain, D.E.; James, D.L. II

1997-01-01

A small-scale demonstration of a new photocatalytic membrane reactor was undertaken at the X-623 Groundwater Treatment Facility at the Portsmouth Gaseous Diffusion Plant. The photocatalytic membrane reactor initially removed between 60 and 65% of the TCE in a single pass. It also removed significant amounts of three additional compounds (including completely removing one of the compounds). It is believed that these compounds were vinyl chloride, and two isomers of dichloroethylene. Within three days from startup, high suspended solids (mainly bacteria) contained in the feedwater tank caused plugging of the system's prefilter. The high concentration of bacteria was the result of a previously unknown large amount of activated carbon present in the feed tank prior to addition of the groundwater. It was also later discovered that fine colloidal silt particles had fouled the photocatalytic membranes and reduced their activity yielding only about a 20% reduction of TCE. The silt particles were determined to be between 50 and 100 nm and were able to pass through the 500 nm (0.5 μm) diameter pores of the prefilter. The results of this field test demonstrated the potential for success of the deployment of this technology, the simplicity, flexibility, and operability of the process and that improvements to the system design are needed prior to any future demonstrations. 9 figs

Evaluation of 10 aliphatic halogenated hydrocarbons in the mouse bone marrow micronucleus test.

Science.gov (United States)

Crebelli, R; Carere, A; Leopardi, P; Conti, L; Fassio, F; Raiteri, F; Barone, D; Ciliutti, P; Cinelli, S; Vericat, J A

1999-03-01

Ten halogenated aliphatic hydrocarbons (carbon tetrachloride, 1-chlorohexane, 2,3-dichlorobutane, 1,2-dichloroethane, 1,2-dichloroethylene, 1,3-dichloropropane, hexachloroethane, 1,1,2-trichloroethane, 1,2,3-trichloropropane and 1,1,3-trichloropropene), previously assayed in genetic assays in fungi, were evaluated in the mouse bone marrow micronucleus test in order to assess their genotoxicity in vivo. All chemicals were administered once i.p. at 40 and 70-80% of their respective LD50 to male and female CD-1 mice, 24 and 48 h before killing. All treatments produced evident clinical symptoms, but no marked depression of bone marrow proliferation. No statistically significant increases in the incidence of micronucleated polychromatic erythrocytes over the control values were observed at any sampling time with any of the 10 halogenated hydrocarbons assayed. The comparison of the results obtained in this study with the findings provided by in vitro micronucleus assays on the same chemicals, reported by other authors, indicate that mouse bone marrow is weakly sensitive to the genotoxic effects induced by halogenated hydrocarbons in other test systems. This suggests that the role of such an assay in carcinogen screening may be questionable for this chemical class. An examination of mouse bone marrow micronucleus test results with the halogenated aliphatic hydrocarbons classified as carcinogens by IARC supports this conclusion.

Determination of volatile organic compounds pollution sources in malaysian drinking water using multivariate analysis.

Science.gov (United States)

Soh, Shiau-Chian; Abdullah, Md Pauzi

2007-01-01

A field investigation was conducted at all water treatment plants throughout 11 states and Federal Territory in Peninsular Malaysia. The sampling points in this study include treatment plant operation, service reservoir outlet and auxiliary outlet point at the water pipelines. Analysis was performed by solid phase micro-extraction technique with a 100 microm polydimethylsiloxane fibre using gas chromatography with mass spectrometry detection to analyse 54 volatile organic compounds (VOCs) of different chemical families in drinking water. The concentration of VOCs ranged from undetectable to 230.2 microg/l. Among all of the VOCs species, chloroform has the highest concentration and was detected in all drinking water samples. Average concentrations of total trihalomethanes (THMs) were almost similar among all states which were in the range of 28.4--33.0 microg/l. Apart from THMs, other abundant compounds detected were cis and trans-1,2-dichloroethylene, trichloroethylene, 1,2-dibromoethane, benzene, toluene, ethylbenzene, chlorobenzene, 1,4-dichlorobenzene and 1,2-dichloro - benzene. Principal component analysis (PCA) with the aid of varimax rotation, and parallel factor analysis (PARAFAC) method were used to statistically verify the correlation between VOCs and the source of pollution. The multivariate analysis pointed out that the maintenance of auxiliary pipelines in the distribution systems is vital as it can become significant point source pollution to Malaysian drinking water.

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

Science.gov (United States)

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. Copyright © 2015 Elsevier Ltd. All rights reserved.

Chemical contamination assessment in mangrove-lined Caribbean coastal systems using the oyster Crassostrea rhizophorae as biomonitor species.

Science.gov (United States)

Aguirre-Rubí, Javier R; Luna-Acosta, Andrea; Etxebarría, Nestor; Soto, Manu; Espinoza, Félix; Ahrens, Michael J; Marigómez, Ionan

2018-05-01

This paper aims to contribute to the use of mangrove cupped oyster, Crassostrea rhizophorae, as a biomonitor species for chemical contamination assessment in mangrove-lined Caribbean coastal systems. Sampling was carried out in eight localities (three in Nicaragua and five in Colombia) with different types and levels of contamination. Oysters were collected during the rainy and dry seasons of 2012-2013 and the tissue concentrations of metals, polycyclic aromatic hydrocarbons (PAHs), and persistent organic pollutants (POPs) were determined. Low tissue concentrations of metals (except Hg) and PAHs; moderate-to-high tissue concentrations of Hg, hexachlorocyclohexanes (HCHs), and dichlorodiphenyl-trichloroethanes (DDTs); detectable levels of chlorpyrifos, polychlorinated biphenyls (PCBs) (mainly CB28, CB118, CB138 and CB 153) and brominated diphenyl ethers 85 (BDE85); and negligible levels of musks were recorded in Nicaraguan oysters. A distinct profile of POPs was identified in Colombia, where the tissue concentrations of PCBs and synthetic musk fragrances were low to moderate, and Ag, As, Cd, Pb, and PAHs ranged from moderate to extremely high. Overall, the values recorded for HCHs, DDTs and PCBs in Nicaraguan mangrove cupped oysters greatly exceeded the reference values in tissues of C. rhizophorae from the Wider Caribbean Region, whereas only the levels of PCBs were occasionally surpassed in Colombia. Different contaminant profiles were distinguished between oysters from Nicaragua and Colombia in radar plots constructed using the main groups of contaminants (metals, PAHs, musks, PCBs, and organochlorine pesticides (OCPs)). Likewise, integrated pollution indices revealed differences in the levels of contaminants. Moreover, the profiles and levels in oyster tissues also varied with season. Thus, principal component analysis clearly discriminated Nicaraguan and Colombian localities and, especially in Colombia, seasonal trends in chemical contamination and differences

Site remediation using photocatalytic VOC destruction of chlorinated hydrocarbons

Energy Technology Data Exchange (ETDEWEB)

Brunet, R.A.H.; Pearcey, R.; Kittrell, J.R.; Mackin, G.; Wise, C.A.

1999-07-01

An innovative environmental technology has been developed and demonstrated for cost-effective control of toxic air emissions, such as trichloroethylene (TCE) and perchloroethylene (PCE), found in soil and groundwater at hazardous waste sites and in industrial effluents. The technology uses UV light and a proprietary photocatalyst to adsorb and destroy pollutants at ambient conditions, even with high humidity. Air stripping and soil vapor extraction efficiently transfer the pollutants to the gas phase, where they can be economically treated by photocatalysis without the risk of hazardous by-product formation. The AIR2000 photocatalytic technology was successfully installed at the Stamina Mills Superfund site in Rhode Island, where a commercial scale unit is treating 700 cfm of up to 1,000 ppm TCE, mixed with PCE, dichloroethylene (DCE), trichloroethane (TCA), and vinyl chloride (VC) produced through a combination of soil vapor extraction (SVE) and air stripping. As part of the EPA SITE program, the system was monitored for overall destruction removal efficiency (DRE) and hazardous by-product formation. A DRE in excess of 99% was reported over the first four months of operation, with greater than 99.99% DRE achieved, without production of hazardous by-products. The operating cost of the system is approximately 20% of activated carbon adsorption, which provides approximately $1,500,000 in cost savings over the life of the Stamina Mills project. The Adsorption Integrated Reaction (AIR) process is the recipient of the 1997 SBIR Technology of the Year award, the 1998 EPA Environmental Technology Innovator Award, and the 1998 R and D 100 Award.

The use of field redox measurements in assessing remediation of ground water containing petroleum hydrocarbons and chlorinated organic compounds

International Nuclear Information System (INIS)

Warner, S.D.; Gallinatti, J.D.; Honniball, J.H.

1995-01-01

Field measurements of the reduction-oxidation (redox) condition of ground water were used to assess the effects of in situ remediation of ground water affected by petroleum hydrocarbons and chlorinated organic compounds at multiple sites in northern California. The redox condition of ground water, traditionally measured quickly and inexpensively using a meter that measures electrode potential (Eh), is a valuable parameter by which to assess the conditions that affect the relative stability of various chemicals in ground water. Although not specific to a given redox couple measurements obtained using the traditional Eh meter give a sense of the relative tendency for a ground water to be reducing or oxidizing by providing a measurement of the system Eh. Two cases demonstrate the use of ground water Eh measurements in assessing the effects of in situ ground water remediation. In the first case, ground water affected by petroleum hydrocarbons-gasoline (TPHg), and benzene, toluene, ethylbenzene, and xylenes (BTEX) (ambient Eh of -100 to +100 millivolts [mv]) was treated by injecting hydrogen peroxide to supply oxygen to the subsurface environment and stimulate microbial activity. The second case involved remediation of ground water containing chlorinated organic compounds. In this case, a subsurface permeable ground water treatment wall containing granular iron was installed across the flow path of the affected ground water. The in situ chemical treatment, which successfully dechlorinates compounds such as trichloroethylene, 1,2-dichloroethylene, and vinyl chloride, caused reducing conditions in the ground water, which resulted in the decrease in ground water Eh from am ambient reading of about -50 mv to about -400 mv

Transboundary pollution: Persistent organochlorine pesticides in migrant birds of the Southwestern United States and Mexico

Science.gov (United States)

Mora, Miguel A.

1997-01-01

The hypothesis that migratory birds accumulate persistent organochlorine pesticides (POPs) during the winter in Latin America has been prevalent for many years, particularly since 1,1,1-trichloro-2,2–bis(p-chlorophenyl)ethane (DDT) was banned in the United States in 1972. It has been suggested that peregrine falcons (Falco peregrinus), black-crowned night herons (Nycticorax nycticorax), white-faced ibises (Plegadis chihi), various migratory waterfowl and shorebirds, and other avian species accumulate higher concentrations of POPs while on migration or on their wintering grounds in Latin America. Nonetheless, the data obtained thus far are limited, and there is no clear pattern to suggest that such accumulation occurs on a widespread basis. In this review wildlife contaminant studies conducted along the U.S.-Mexico border and throughout Mexico are discussed. The results for the most part seem to indicate that no major accumulation of 2,2-bis(p-chlorophenyl)-1,1-dichloroethylene) (DDE), the most persistent organochlorine compound, has occurred or been reported for most parts of Mexico. The majority of the DDE values in birds from Mexico were similar to those reported in birds from the southwestern United States during the same years. More work needs to be done, particularly in those cotton-producing areas of Mexico where DDT was applied heavily in the past (e.g., Chiapas and Michoacan). Because DDT is still used for malaria control and may still be used in agriculture in Chiapas, this state is probably the one where most migrant species would still be at a significant risk of increased accumulation of DDE and DDT.

Numerical examination of the factors controlling DNAPL migration through a single fracture.

Science.gov (United States)

Reynolds, D A; Kueper, B H

2002-01-01

The migration of five dense nonaqueous phase liquids (DNAPLs) through a single fracture in a clay aquitard was numerically simulated with the use of a compositional simulator. The effects of fracture aperture, fracture dip, matrix porosity, and matrix organic carbon content on the migration of chlorobenzene, 1,2-dichloroethylene, trichloroethylene, tetra-chloroethylene, and 1,2-dibromoethane were examined. Boundary conditions were chosen such that DNAPL entry into the system was allowed to vary according to the stresses applied. The aperture is the most important factor of those studied controlling the migration rate of DNAPL through a single fracture embedded in a clay matrix. Loss of mass to the matrix through diffusion does not significantly retard the migration rate of the DNAPL, particularly in larger aperture fractures (e.g., 50 microm). With time, the ratio of diffusive loss to the matrix to DNAPL flux into the fracture approaches an asymptotic value lower than unity. The implication is that matrix diffusion cannot arrest the migration of DNAPL in a single fracture. The complex relationships between density, viscosity, and solubility that, to some extent, govern the migration of DNAPL through these systems prevent accurate predictions without the use of numerical models. The contamination potential of the migrating DNAPL is significantly increased through the transfer of mass to the matrix. The occurrence of opposite concentration gradients within the matrix can cause dissolved phase contamination to exist in the system for more than 1000 years after the DNAPL has been completely removed from the fracture.

Impedimetric microbial biosensor based on single wall carbon nanotube modified microelectrodes for trichloroethylene detection

International Nuclear Information System (INIS)

Hnaien, M.; Bourigua, S.; Bessueille, F.; Bausells, J.; Errachid, A.; Lagarde, F.; Jaffrezic-Renault, N.

2011-01-01

Highlights: ► We propose an impedimetric microbial biosensor for trichloroethylene detection. ► A new transducer modified with carbon nanotubes and Pseudomonas putida is evaluated. ► Functionalization steps are controlled by impedance spectroscopy and AFM. ► The biosensor offers good sensitivity, selectivity, linear range and stability. ► The biosensor is successfully applied to spiked natural water samples. - Abstract: Contamination of soils and groundwaters with persistent organic pollutants is a matter of increasing concern. The most common organic pollutants are chlorinated hydrocarbons such as perchloroethylene and trichloroethylene (TCE). In this study, we developed a bacterial impedimetric biosensor for TCE detection, based on the immobilization of Pseudomonas putida F1 strain on gold microelectrodes functionalized with single wall carbon nanotubes covalently linked to anti-Pseudomonas antibodies. The different steps of microelectrodes functionalization were characterized by electrochemical impedance and atomic force spectroscopies, and analytical performances of the developed microbial biosensor were determined. The impedimetric biosensor response was linear with TCE concentration up to 150 μg L −1 and a low limit of detection (20 μg L −1 ) was achieved. No significant loss of signal was observed after 4 weeks of storage at 4 °C in phosphate buffer saline pH 7 (three to four measurements a week). After 5 weeks, 90% of the initial value still remained. cis-1,2-Dichloroethylene and vinylchloride, the main TCE degradation products, did not significantly interfere with TCE. The microbial sensor was finally applied to the determination of TCE in natural water samples spiked at the 30, 50 and 75 μg L −1 levels. Recoveries were very good, ranging from 100 to 103%.

Analysis of dechlorination kinetics of chlorinated aliphatic hydrocarbons by Fe(II) in cement slurries

Energy Technology Data Exchange (ETDEWEB)

Jung, Bahngmi [Department of Earth and Environmental Sciences, Wright State University, Dayton, OH 45435-0001 (United States)], E-mail: jung.bahngmi@gmail.com; Batchelor, Bill [Department of Civil Engineering, Texas A and M University, College Station, TX 77843-3136 (United States)

2008-03-21

Degradative solidification/stabilization with ferrous iron (DS/S-Fe(II)) has been found to be effective in degrading a number of chlorinated aliphatic hydrocarbons including 1,1,1-trichloroethane (1,1,1-TCA), 1,1,2,2-tetrachloroethane (1,1,2,2-TeCA), tetrachloroethylene (PCE), trichloroethylene (TCE), 1,1-dichloroethylene (1,1-DCE), vinyl chloride (VC), carbon tetrachloride (CT) and chloroform (CF). Previous studies have characterized degradation kinetics in DS/S-Fe(II) systems as affected by Fe(II) dose, pH and initial target organic concentration. The goal of this study is to investigate the importance of various chemical properties on degradation kinetics of DS/S-Fe(II). This was accomplished by first measuring rate constants for degradation of 1,1,1-TCA, 1,1,2,2-TeCA and 1,2-dichloroethane (1,2-DCA) in individual batch experiments. Rate constants developed in these experiments and those obtained from the literature were related to thermodynamic parameters including one-electron reduction potential, two-electron reduction potential, bond dissociation energy and lowest unoccupied molecular orbital energies. Degradation kinetics by Fe(II) in cement slurries were generally represented by a pseudo-first-order rate law. The results showed that the rate constants for chlorinated methanes (e.g. CT, CF) and chlorinated ethanes (e.g. 1,1,1-TCA) were higher than those for chlorinated ethylenes (e.g. PCE, TCE, 1,1-DCE and VC) under similar experimental conditions. The log of the pseudo-first-order rate constant (k) was found to correlate better with lowest unoccupied molecular orbital energies (E{sub LUMO}) (R{sup 2} = 0.874) than with other thermodynamic parameter descriptors.

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

Energy Technology Data Exchange (ETDEWEB)

Fan Chihhao [Department of Safety, Health, and Environmental Engineering, Mingchi University of Technology, Taipei County, Taiwan (China); Wang, G.-S. [Department of Public Health, National Taiwan University, Taipei, Taiwan (China); Chen, Y.-C. [Energy and Environment Research Laboratories, Industrial Technology Research Institute, Hsinchu County, Taiwan (China); Ko, C.-H. [School of Forest and Resources Conservation, National Taiwan University, Taipei, Taiwan (China)], E-mail: chunhank@ntu.edu.tw

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 {mu}g/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.

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

International Nuclear Information System (INIS)

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

1995-01-01

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

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

Science.gov (United States)

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. Copyright © 2011. Published by Elsevier Ltd.

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

Science.gov (United States)

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.

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

Science.gov (United States)

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.

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

Science.gov (United States)

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

An investigation into the activation and deactivation of chlorinated hydrocarbons to genotoxins in metabolically competent human cells.

Science.gov (United States)

Doherty, A T; Ellard, S; Parry, E M; Parry, J M

1996-05-01

We have investigated the induction of micronuclei by 15 chlorinated hydrocarbons in the cytochalasin B-blocked micronucleus assay utilizing genetically engineered cell lines. The human lymphoblastoid cell line AHH-1, with native cytochrome CYP1A1 activity, the MCL-5 cell line, which stably expresses cDNAs encoding human CYP1A2, 2A6, 3A4, 2E1 and microsomal epoxide hydrolase, and the h2E1 cell line, containing a cDNA for CYP2E1, were used in this study. We have demonstrated the induction of kinetochore-positive micronuclei by two chlorinated solvents, 2,3-dichlorobutane and 1,1, 2-trichloroethane, in the metabolically competent cell lines MCL-5 and h2E1. The MCL-5 and h2E1 cell lines have in addition shown the capacity to produce metabolites in the presence of methylene chloride, carbon tetrachloride, 1,2,3-trichloropropane, tetrachloroethylene, toluene and n-hexane, wich yield elevated micronucleus frequencies compared with the parental cell line AHH-1. Hexachloroethane failed to induce micronuclei in any of the cell lines and 1,2-dichloroethane and 1-chlorohexane induced micronuclei without the requirement for metabolic activation in all three cell lines. The MCL-5 cell line exhibited reduced micronucleus frequencies compared with the AHH-1 and h2E1 cell lines following exposure to 1,2-dichloroethylene, 1,3-dichloropropane, 1,1, 1-trichloroethane and 1,2,3-trichloropropane. The methodology used has shown the ability of metabolically competent cell lines expressing cDNAs encoding the cytochrome P450 isoenzymes to metabolize halogenated hydrocarbons to genotoxic species, including both clastogens and aneugens. The biotransformation of chemicals to aneugenic species has not previously been demonstrated.

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

International Nuclear Information System (INIS)

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

2016-01-01

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. - Highlights: • Cucurbita pepo accumulates DDE and can be used for phytoremediation. • Phytoremediation capacity might be enhanced with endophytic bacteria. • The differences in bacterial communities without and with DDE are investigated. • Several DDE-tolerant bacteria are discovered and might be used in phytoremediation. - DDE-exposure and DDE-uptake of Cucurbita pepo lead to increases in both diversity

Hanford Site groundwater monitoring for Fiscal Year 1997

Energy Technology Data Exchange (ETDEWEB)

Hartman, M.J.; Dresel, P.E. [eds.] [and others

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.

Prenatal organochlorine compound exposure, rapid weight gain, and overweight in infancy.

Science.gov (United States)

Mendez, Michelle A; Garcia-Esteban, Raquel; Guxens, Mónica; Vrijheid, Martine; Kogevinas, Manolis; Goñi, Fernando; Fochs, Silvia; Sunyer, Jordi

2011-02-01

Although it has been hypothesized that fetal exposure to endocrine-disrupting chemicals may increase obesity risk, empirical data are limited, and it is uncertain how early in life any effects may begin. We explored whether prenatal exposure to several organochlorine compounds (OCs) is associated with rapid growth in the first 6 months of life and body mass index (BMI) later in infancy. Data come from the INMA (Infancia y Medio-Ambiente) Child and Environment birth cohort in Spain, which recruited 657 women in early pregnancy. Rapid growth during the first 6 months was defined as a change in weight-for-age z-scores > 0.67, and elevated BMI at 14 months, as a z-score ≥ the 85th percentile. Generalized linear models were used to estimate the risk of rapid growth or elevated BMI associated with 2,2-bis(p-chlorophenyl)-1,1-dichloroethylene (DDE), hexachlorobenzene, β-hexachlorohexane, and polychlorinated biphenyls in first-trimester maternal serum. After multivariable adjustment including other OCs, DDE exposure above the first quartile was associated with doubling of the risk of rapid growth among children of normal-weight (BMI < 25 kg/m2), but not overweight, mothers. DDE was also associated with elevated BMI at 14 months (relative risk per unit increase in log DDE = 1.50; 95% confidence interval, 1.11-2.03). Other OCs were not associated with rapid growth or elevated BMI after adjustment. In this study we found prenatal DDE exposure to be associated with rapid weight gain in the first 6 months and elevated BMI later in infancy, among infants of normal-weight mothers. More research exploring the potential role of chemical exposures in early-onset obesity is needed.

Apoptosis (programmed cell death) as an indicator of xenobiotic toxicity

International Nuclear Information System (INIS)

Bond, G.P.

1989-01-01

Xenobiotics alter the frequency and pattern of apoptosis (programmed cell death). Preliminary studies identified the mouse liver, with normally low levels of apoptosis, as a preferable test system to the chicken embryo limb, with normally high levels of apoptosis. The major purposes of these investigations, using the apoptogen and necrogen 1,1-dichloroethylene (DCE), were to determine if increases in apoptosis, (1) could be quantified as a direct result of treatment, (2) were dose- and time-dependent, (3) were independent of necrosis, (4) were associated with mitosis in the control of cell numbers and (5) were limited to specific areas of the liver. To these ends, food-deprived female, CF-1 mice were administered DCE ip under varying experimental conditions. Increased apoptosis occurred in a dose- and time-dependent manner after treatment with 12.5, 40, and 125 mg/kg for 0.5, 1, 2, 4 and 8 hr. Peak effects were observed at 4 hr. Apoptosis occurred only in the midzonal/pericentral areas of the liver. At 12.5 mg/kg, there were no effects on biochemical (alanine transaminase) and morphological indices of necrosis, establishing apoptosis as a separate phenomenon from necrosis. Increased 3 H-thymidine incorporation (DNA synthesis), mitosis and the percentage of octaploid hepatocytes occurred from 24-48 hr after treatment with the apoptotic but non-necrotic dose of 40 mg/kg. Apoptosis only occurred in the midzonal/pericentral areas of the liver after multiple doses with DCE, indicating the zonal selectivity of the response. In conclusion, apoptosis, a normally occurring homeostatic process associated with mitosis in the control of cell numbers, is affected by selected xenobiotics in a dose-dependent manner. Xenobiotic-induced apoptosis in the liver occurs at low doses of xenobiotics which cause no other effects on tissue structure or function

Reduced systemic toxicity and preserved vestibular toxicity following co-treatment with nitriles and CYP2E1 inhibitors: a mouse model for hair cell loss.

Science.gov (United States)

Saldaña-Ruíz, Sandra; Boadas-Vaello, Pere; Sedó-Cabezón, Lara; Llorens, Jordi

2013-10-01

Several nitriles, including allylnitrile and cis-crotononitrile, have been shown to be ototoxic and cause hair cell degeneration in the auditory and vestibular sensory epithelia of mice. However, these nitriles can also be lethal due in large part to the microsomal metabolic release of cyanide, which is mostly dependent on the activity of the 2E1 isoform of the cytochrome P450 (CYP2E1). In this study, we co-administered mice with a nitrile and, to reduce their lethal effects, a selective CYP2E1 inhibitor: diallylsulfide (DAS) or trans-1,2-dichloroethylene (TDCE). Both in female 129S1/SvImJ (129S1) mice co-treated with DAS and cis-crotononitrile and in male RjOrl:Swiss/CD-1 (Swiss) mice co-treated with TDCE and allylnitrile, the nitrile caused a dose-dependent loss of vestibular function, as assessed by a specific behavioral test battery, and of hair cells, as assessed by hair bundle counts using scanning electron microscopy. In the experiments, the CYP2E1 inhibitors provided significant protection against the lethal effects of the nitriles and did not diminish the vestibular toxicity as assessed by behavioral effects in comparison to animals receiving no inhibitor. Additional experiments using a single dose of allylnitrile demonstrated that TDCE does not cause hair cell loss on its own and does not modify the vestibular toxicity of the nitrile in either male or female 129S1 mice. In all the experiments, high vestibular dysfunction scores in the behavioral test battery predicted extensive to complete loss of hair cells in the utricles. This provides a means of selecting animals for subsequent studies of vestibular hair cell regeneration or replacement.

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

Energy Technology Data Exchange (ETDEWEB)

Elliott, John E. [Environment Canada, Science & Technology Branch, Pacific Wildlife Research Centre, Delta, British Columbia V4K 3N2 (Canada); Department of Biological Science, Simon Fraser University, Burnaby, BC V5A 1S6 (Canada); Brogan, Jason [Department of Biological Science, Simon Fraser University, Burnaby, BC V5A 1S6 (Canada); Lee, Sandi L. [Environment Canada, Science & Technology Branch, Pacific Wildlife Research Centre, Delta, British Columbia V4K 3N2 (Canada); Drouillard, Ken G. [Great Lakes Institute for Environmental Research, University of Windsor, Windsor, ON N9B 3P4 (Canada); Elliott, Kyle H. [Department of Natural Resource Sciences, McGill University, Ste. Anne de Bellevue, Quebec H9X 3V9 (Canada)

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 197,000 ng/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{sup 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. - Highlights: • As urban areas expand, many animal species are adapting and invading urban areas. • Urban colonists encounter many new stressors, especially chemical pollution. • Urban birds of prey in Canada had high levels of brominated flame retardants (PBDEs). • One individual had the highest level of PBDEs ever recorded for wildlife. • Such high levels may have had toxicological implications.

OECD validation of the Hershberger assay in Japan: phase 2 dose response of methyltestosterone, vinclozolin, and p,p'-DDE.

Science.gov (United States)

Yamasaki, Kanji; Sawaki, Masakuni; Ohta, Ryo; Okuda, Hirokazu; Katayama, Seiichi; Yamada, Tomoya; Ohta, Takafumi; Kosaka, Tadashi; Owens, William

2003-01-01

The Organisation for Economic Co-operation and Development has initiated the development of new guidelines for the screening and testing of potential endocrine disruptors. The Hershberger assay is one of the assays selected for validation based on the need for in vivo screening to detect androgen agonists or antagonists by measuring the response of five sex accessory organs and tissues of castrated juvenile male rats: the ventral prostate, the seminal vesicles with coagulating glands, the levator ani and bulbocavernosus muscle complex, the Cowper's glands, and the glans penis. The phase 1 feasibility demonstration stage of the Hershberger validation program has been successfully completed with a single androgen agonist and a single antagonist as reference substances. The phase 2 validation program employs a range of additional androgen agonists and antagonists as well as 5alpha-reductase inhibitors. Seven Japanese laboratories have contributed phase 2 validation studies of the Hershberger assay using methyltestosterone, vinclozolin, and 2,2-bis (4-chlorophenyl)-1,1-dichloroethylene (p,p'-DDE). The methyltestosterone doses were 0, 0.05, 0.5, 5, and 50 mg/kg/day, and the vinclozolin and p,p'-DDE doses were 0, 3, 10, 30, and 100 mg/kg/day. All chemicals were orally administered by gavage for 10 consecutive days. In the antagonist version of the assay using vinclozolin and p,p'-DDE, 0.2 mg/kg/day of testosterone propionate was coadministered by subcutaneous injection. All five accessory sex preproductive organs and tissues consistently responded with statistically significant changes in weight within a narrow window. Therefore, the Japanese studies support the Hershberger assay as a reliable and reproducible screening assay for the detection of androgen agonistic and antagonistic effects. PMID:14644666

Hanford Site groundwater monitoring for Fiscal Year 1997

International Nuclear Information System (INIS)

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

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

International Nuclear Information System (INIS)

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

2015-01-01

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 197,000 ng/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. - Highlights: • As urban areas expand, many animal species are adapting and invading urban areas. • Urban colonists encounter many new stressors, especially chemical pollution. • Urban birds of prey in Canada had high levels of brominated flame retardants (PBDEs). • One individual had the highest level of PBDEs ever recorded for wildlife. • Such high levels may have had toxicological implications

Serum levels of organochlorine pesticides in the French adult population: the French National Nutrition and Health Study (ENNS), 2006-2007.

Science.gov (United States)

Saoudi, Abdessattar; Fréry, Nadine; Zeghnoun, Abdelkrim; Bidondo, Marie-Laure; Deschamps, Valérie; Göen, Thomas; Garnier, Robert; Guldner, Laurence

2014-02-15

Although most organochlorine (OC) pesticides were banned in France in the 1970s and 1980s, they remain a source of public concern. Because of their high persistence in the environment, they are still detected in foodstuffs, leading to continued human exposure. The purpose of this study was to assess the distribution of serum organochlorine (OC) pesticides in the French adult population and to identify the main risk factors for p,p'-dichlorodiphenyl dichlorethylene (DDE), β-hexachlorocyclohexane (β-HCH) and hexachlorobenzene (HCB). The selected OC pesticides (HCB, DDE, DDT, α-HCH, β-HCB and γ-HCH) were measured in serum samples collected in 2006-2007 from 386 persons (aged 18-74 years) randomly selected among the participants in the clinical and biological component of the French Nutrition and Health Survey (Etude Nationale Nutrition Santé [ENNS]), a cross-sectional survey carried out in the general population. Collected data included biological samples, socio-demographic characteristics, and data about environmental and occupational exposure factors. Of the six OC pesticides investigated, the highest concentrations were observed for HCB, β-HCH and DDE. Median serum concentrations were as follows: 22.8 ng/g lipid for HCB, 0.74 and 27.0 ng/g lipid, respectively, for α- and ß-HCH, and 3.8 and 104.6 ng/g lipid, respectively, for DDT and DDE. Lindane (γ-HCH) was detected in approximately 10% of the sample. OC pesticide levels in serum in French adults were higher (except for DDT and DDE) than those observed in American, Canadian and German populations and generally lower than or in the same range as those observed in other European countries. The low serum DDT/DDE ratio in the present study (3.7%) would suggest that the concentrations observed for these two OC pesticides were mainly the result of past exposure. The most important predictors of serum DDE, HCB and β-HCH concentrations among the French adult population included individual factors (age, gender

Methanogenic community development in anaerobic granular bioreactors treating trichloroethylene (TCE)-contaminated wastewater at 37 °C and 15 °C.

Science.gov (United States)

Siggins, Alma; Enright, Anne-Marie; O'Flaherty, Vincent

2011-04-01

Four expanded granular sludge bed (EGSB) bioreactors were seeded with a mesophilically-grown granular sludge and operated in duplicate for mesophilic (37 °C; R1 & R2) and low- (15°; R3 & R4) temperature treatment of a synthetic volatile fatty acid (VFA) based wastewater (3 kg COD m(-3) d(-1)) with one of each pair (R1 & R3) supplemented with increasing concentrations of trichloroethylene (TCE; 10, 20, 40, 60 mg l(-1)) and one acting as a control. Bioreactor performance was evaluated by % COD removal efficiency and % biogas methane (CH(4)) content. Quantitative Polymerase Chain Reaction (qPCR) was used to investigate the methanogenic community composition and dynamics in the bioreactors during the trial, while specific methanogenic activity (SMA) and toxicity assays were utilized to investigate the activity and TCE/dichloroethylene (DCE) toxicity thresholds of key trophic groups, respectively. At both 37 °C and 15 °C, TCE levels of 60 mg l(-1) resulted in the decline of % COD removal efficiencies to 29% (Day 235) and 37% (Day 238), respectively, and in % biogas CH(4) to 54% (Day 235) and 5% (Day 238), respectively. Despite the inhibitory effect of TCE on the anaerobic digestion process, the main drivers influencing methanogenic community development, as determined by qPCR and Non-metric multidimensional scaling analysis, were (i) wastewater composition and (ii) operating temperature. At the apical TCE concentration both SMA and qPCR of methanogenic archaea suggested that acetoclastic methanogens were somewhat inhibited by the presence of TCE and/or its degradation derivatives, while competition by dechlorinating organisms may have limited the availability of H(2) for hydrogenotrophic methanogenesis. In addition, there appeared to be an inverse correlation between SMA levels and TCE tolerance, a finding that was supported by the analysis of the inhibitory effect of TCE on two additional biomass sources. The results indicate that low-temperature anaerobic

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

Science.gov (United States)

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.

Yield and quality of ground water from stratified-drift aquifers, Taunton River basin, Massachusetts : executive summary

Science.gov (United States)

Lapham, Wayne W.; Olimpio, Julio C.

1989-01-01

locations revealed that 13 of the sample contained one or more of the following compounds: chloroform; carbon tetrachloride; dichloroethane; dichloroethylene; tetrachloroethylene; and, toluene. (Lantz-PTT)

Organochlorine exposure and breast cancer risk in Colombian women Exposição a organoclorados e risco de câncer de mama em mulheres colombianas

Directory of Open Access Journals (Sweden)

P. Olaya-Contreras

1998-01-01

Full Text Available An epidemiological study was performed in Santafé de Bogotá, Colombia, with a total of 306 women enrolled, including 153 incident BC cases and 153 age-matched controls. The objective of this study was to evaluate the association between BC risk and serum dichlorodiphenyl-dichloroethene (DDE levels. Sociodemographic and reproductive data, diet, and past exposure to pesticides were obtained through a structured questionnaire. Chemical analysis of samples was performed by high resolution gas chromatography-ECD. Likelihood of developing BC by exposure to these substances was evaluated through odds ratios (OR adjusted for: first-child breast-feeding, family BC history, body mass index (BMI, parity, and menopausal status. Data analysis was performed by conditional logistic regression techniques. Adjusted OR for exposure to serum DDE and BC suggests an increase risk of BC in the higher category of DDE exposure (OR = 1.95; CI 1.10-3.52. The test for trend was not statistically significant (p = 0.09. We confirm that serum DDE levels bear a positive association to risk of BC and could support the association between risk of BC and burden of DDE exposure.Em estudo epidemiológico realizado em Santa Fé de Bogotá, Colômbia, 153 casos incidentes de câncer de mama (CM foram comparados com 153 controles, pareados por idade. O objetivo deste estudo foi avaliar a associação entre o risco de CM e níveis séricos do pesticida DDT (DDE. Dados reprodutivos e sócio-demográficos, características da dieta e informação sobre exposição pregressa a pesticidas foram obtidos por meio de questionário. A análise química de amostras de sangue foi realizada através de cromatografia a gaz de alta resolução - ECD. A verossimelhança de desenvolver CM como decorrência de exposição a estas substâncias foi avaliada através de odds ratios (OR, obtidas por técnicas de regressão logística condicional, ajustadas para amamentação do primogênito, hist

Fish consumption and plasma levels of organochlorines in a female population in Northern Norway.

Science.gov (United States)

Furberg, Anne-Sofie; Sandanger, Torkjel; Thune, Inger; Burkow, Ivan C; Lun, Eiliv

2002-02-01

Increased cancer incidence and mortality have been found among humans exposed to high levels of organochlorines (OCs), either accidentally or as industrial workers. In order to assess levels of OCs in Norwegian women north of the Arctic Circle and validate self-reported fish consumption as a surrogate measure of organochlorine body burden, concentrations of seven polychlorinated biphenyl (PCB) congeners [IUPAC Nos. CB-105, CB-118, CB-138 (+ CB-163), CB-153, CB-180, CB-183, CB-187], beta-hexachlorocyclohexane (beta-HCH), 2,2'-bis(p-chlorophenyl)-1,1-dichloroethylene (p,p'-DDE) and cis- and trains-chlordane (c-CD and t-CD) were examined in plasma samples of middle-aged women attending for health screening. Altogether, 47 of those invited (81%) completed a questionnaire and donated a suitable blood sample. The ability of questionnaire data to predict plasma levels of OCs was tested in linear and logistic regression analyses. Measured plasma concentrations were in the range reported for the general female population of other Western countries and the relative amounts of PCBs were similar to the circumpolar pattern. Intake of seagulls' eggs was a predictor of PCB congeners CB-138 (+CB-163) (p<0.05) and CB-153 (p<0.01). No other food category was positively associated with any compound. In contrast, duration of residence in the study municipality, body mass index (BMI) and lifetime lactation (months) were the best univariate predictors. There was an increase in beta-HCH, p,p'-DDE and most of the PCBs (p<0.05 for all) with increasing length of time a subject had lived in the municipality. BMI was a positive predictor for beta-HCH (OR=3.10, 95% CI 1.50-6.43, per 5 kgm(-2)), chlordane (OR=2.13, 95% CI 1.12-4.05, per 5 kgm(-2)) and CB-105 and CB-153 (p<0.05 for both). Lactation was negatively associated with all OCs (p<0.05), except chlordane and two of the PCB congeners. Time living in the municipality and lactation explained 34%, of the variance in concentration of total

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

Energy Technology Data Exchange (ETDEWEB)

NONE

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.

Ground-water contamination at Wurtsmith Air Force Base, Michigan

Science.gov (United States)

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

1983-01-01

A sand and gravel aquifer of glacial origin underlies Wurtsmith Air Force Base in northeastern lower Michigan. The aquifer overlies a thick clay layer at an average depth of 65 feet. The water table is about 10 feet below land surface in the western part of the Base and about 25 feet below land surface in the eastern part. A ground-water divide cuts diagonally across the Base from northwest to southeast. South of the divide, ground water flows to the Au Sable River; north of the divide, it flows to Van Etten Creek and Van Etten Lake. Mathematical models were used to aid in calculating rates of groundwater flow. Rates range from about 0.8 feet per day in the eastern part of the Base to about 0.3 feet per day in the western part. Models also were used as an aid in making decisions regarding purging of contaminated water from the aquifer. In 1977, trichloroethylene was detected in the Air Force Base water-supply system. It had leaked from a buried storage tank near Building 43 in the southeastern part of the Base and moved northeastward under the influence of the natural ground-water gradient and the pumping of Base water-supply wells. In the most highly contaminated part of the plume, concentrations are greater than 1,000 micrograms per liter. Current purge pumping is removing some of the trichloroethylene, and seems to have arrested its eastward movement. Pumping of additional purge wells could increase the rate of removal. Trichloroethylene has also been detected in ground water in the vicinity of the Base alert apron, where a plume from an unknown source extends northeastward off Base. A smaller, less well-defined area of contamination also occurs just north of the larger plume. Trichloroethylene, identified near the waste-treatment plant, seepage lagoons, and the northern landfill area, is related to activities and operations in these areas. Dichloroethylene and trichloroethylene occur in significant quantities westward of Building 43, upgradient from the major

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

Science.gov (United States)

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

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

International Nuclear Information System (INIS)

1999-01-01

.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

In situ remediation of chlorinated solvent-contaminated groundwater using ZVI/organic carbon amendment in China: field pilot test and full-scale application.

Science.gov (United States)

Yang, Jie; Meng, Liang; Guo, Lin

2018-02-01

Chlorinated solvents in groundwater pose threats to human health and the environment due to their carcinogenesis and bioaccumulation. These problems are often more severe in developing countries such as China. Thus, methods for chlorinated solvent-contaminated groundwater remediation are urgently needed. This study presents a technique of in situ remediation via the direct-push amendment injection that enhances the reductive dechlorination of chlorinated solvents in groundwater in the low-permeability aquifer. A field-based pilot test and a following real-world, full-scale application were conducted at an active manufacturing facility in Shanghai, China. The chlorinated solvents found at the clay till site included 1,1,1-trichloroethane (1,1,1-TCA), 1,1-dichloroethane (1,1-DCA), 1,1-dichloroethylene (1,1-DCE), vinyl chloride (VC), and chloroethane (CA). A commercially available amendment (EHC ® , Peroxychem, Philadelphia, PA) combining zero-valent iron and organic carbon was used to treat the above pollutants. Pilot test results showed that direct-push EHC injection efficiently facilitated the in situ reductive remediation of groundwater contaminated with chlorinated solvents. The mean removal rates of 1,1,1-TCA, 1,1-DCA, and 1,1-DCE at 270 days post-injection were 99.6, 99.3, and 73.3%, respectively, which were obviously higher than those of VC and CA (42.3 and 37.1%, respectively). Clear decreases in oxidation-reduction potential and dissolved oxygen concentration, and increases in Fe 2+ and total organic carbon concentration, were also observed during the monitoring period. These indicate that EHC promotes the anaerobic degradation of chlorinated hydrocarbons primarily via long-term biological reductive dechlorination, with instant chemical reductive dechlorination acting as a secondary pathway. The optimal effective time of EHC injection was 0-90 days, and its radius of influence was 1.5 m. In full-scale application, the maximum concentrations of 1,1,1-TCA

Monitoring the decontamination of a site polluted by DNAPLs

Science.gov (United States)

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

Hanford Site Groundwater Monitoring for Fiscal Year 1998

Energy Technology Data Exchange (ETDEWEB)

Hartman, M.J. [and others

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

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

Science.gov (United States)

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.

Hanford Site Groundwater Monitoring for Fiscal Year 1999

Energy Technology Data Exchange (ETDEWEB)

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

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

Energy Technology Data Exchange (ETDEWEB)

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

Study on decomposition and removal of organic pollutants in gases using electron beams

International Nuclear Information System (INIS)

Hakoda, Teruyuki

2006-01-01

Volatile organic compounds (VOC) used as solvents and de-oil reagents have been emitted to the atmosphere and oxidized subsequently into toxic photochemical oxidants in the atmosphere. Reduction of the emission of VOC has been required under law and regulations for factories/plants at which huge amounts of VOC are used. The electron beam (EB) treatment is suitable for purification of high flow-rate ventilation air containing dilute VOC emitted from such factories/plants. The purification processes of such ventilation air have been developed based on the decomposition reactions and property changes of VOC. The results for chloro-ethylenes and aromatic hydrocarbons, which have been emitted with abundant quantities, are introduced in the present paper. Chloroethylenes, except for monochloroethylene, were oxidized into water-soluble primary products through chain reactions in EB irradiated humid air. The chain oxidation reactions of such chloro-ethylenes were initiated exclusively by a reaction with OH radicals, but electron-attachment dissociation under EB irradiation. Gas-phase termination reactions involved the bimolecular reaction of alkylperoxyl radicals for tri- and di-chloroethylenes, and the reaction of alkylperoxyl radicals and alkyl radicals beside such a bimolecular reaction for tetrachloroethylene. The deposition of the alkyl-peroxyl radicals on an irradiation vessel wall also terminated the chain oxidation reactions. The solid-phase termination reaction was negligible to the gas-phase termination reactions under irradiation with high-dose rate so that the oxidation of chloro-ethylenes was achieved with lower doses under high-dose rate irradiation like EB irradiation. The hydrolysis of the primary products combined with EB irradiation is prospective to be applied to the purification of chloroethylenes/air mixtures with lower doses. Under irradiation of aromatic hydrocarbons/air mixtures, toxic and oxidation-resistant particles with mean diameters of a few

Occurrence and removal of volatile organic compounds (VOC) relative to water treatment plants in Malaysia

International Nuclear Information System (INIS)

Soh Shiau Chian

2005-01-01

pollution, the overall atmosphere in water treatment plant and the material used in water treatment processes should also be noted. This is because VOC compounds such as 1,1-dichloroethane, 1,2-dichloroethylene, 1,3-dichloropropene, 2,2-dichloropropane and methylene chloride concentrations were found increased in setteled and filtered water samples. This study also used chemometric analysis method such as principal component analysis (PCA) with the aid of varimax rotation, and parallel factor analysis (PARAFAC) method to verify the correlation between VOC compounds and the source of pollution, statistically. Chemometric results suggested that the drinking water quality did not only depend on the quality of its raw water and treatment processes involved but also relied on the effectiveness of the distribution system. On the study in Semenyih Catchment, three tributaries of Semenyih River, namely Saringgit River, Rinching River and Beranang River were held responsible for pollution. On the other hand, chemometric analysis also confirmed that the pollution of VOC compounds occurred during sedimentation and filtration process in treatment plant, which also indicated that the Semenyih River water treatment plant did not remove VOC compounds. Thus, it is suggested that granulated activated carbon (GAC) and tower aeration (PTA) are used as part of the water treatment process in order to remove VOC compounds. (author)

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

Science.gov (United States)

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

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

Science.gov (United States)

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 may have become contaminated at least partly because of enhanced vertical migration associated with the pumping of and (or) direct migration down deep well bores. Except for TCE in the sample from a shallow monitoring well, all detections of VOCs were at concentrations below Maximum Contaminant Levels (MCLs) set by the U.S. Environmental Protection Agency. Concentrations of all VOCs detected in the supply wells were less than one-tenth of the corresponding MCLs. However, the presence of VOCs in all but deep groundwater, including the detection of chloroform (a chlorination byproduct) in several shallow wells, indicates that groundwater in the study area commonly is affected by human activities, even to substantial depths. The only natural contaminant detected at concentrations near or above its MCL was arsenic, which has been detected at elevated concentrations across broad areas of the MRGB. Concentrations of arsenic, present primarily as arsenate, exceeded the MCL of 10 micrograms per liter (μg/L) in water from the two deep wells (one of which had the highest concentration, 35 μg/L), from one intermediate well, and from two supply wells, including the SSW. Water-quality and solid-phase data from this study are consistent with elevated arsenic concentrations in groundwater being related to pH-dependent desorption of arsenic from ferric oxyhydroxides in sediments in deep parts of the aquifer. Concentrations of nitrate ranged between 1.3 and 5.4 milligrams per liter (mg/L) in water from shallow wells screened across the water table, but were less than 0.9 mg/L in water from all but one deeper well. Nitrogen isotopes and chloride/bromide ratios for shallow wells were consistent with natural soil nitrogen. Nitrate concentrations and nitrogen isotopes indicated that denitrification is occurring at intermediate aquifer depths, and that the progress of the denitrification reaction

Davis Pond freshwater prediversion biomonitoring study: freshwater fisheries and eagles

Science.gov (United States)

Jenkins, Jill A.; Bourgeois, E. Beth; Jeske, Clint W.

2008-01-01

assessed possible influx of contaminants with the freshwater diversion, contaminant levels in fishes and bivalves in this study were generally lower, yet three nontoxic inorganic elements in Davis Pond fish samples exhibited ranges of concentrations that were more than two times higher than did those from Caernarvon. Levels in bivalves were different between diversions but about equal in the numbers of trace elements showing high levels per location. Contaminant values were compared to those listed in various literature and agency sources, both regional and national, including the National Contaminant Biomonitoring Program (NCBP), in which the 85th percentile and above represents what is considered to be an elevated contaminant concentration and cause for concern. Generally, bivalves were at the high end of their ranges for both organic and inorganic contaminants. In this study, OCs were detectable in 67 percent of fish from the Mississippi River site, ranging from 0.15 to 1.09 μg/g wet weight (ww) or fresh weight (fw), and in 11 percent of the fish from the marsh sites, ranging from 0.06 to 0.612 μg/g ww. Bivalves from the Mississippi River had OC levels of 0.096 μg/g ww, whereas none were detectable in bivalves at the marsh sites. In this study, p,p’-dichlorodiphenyldichloroethylene (p,p’-DDE) (a biodegradation product of DDT [dichlorodiphenyl trichloroethane]) and total PCBs were the most frequently detected OCs and were primarily from the Mississippi River. For total OC content, using adjusted least squares means, some significant interactions were noted between fish species and sites. PAHs were detected in aquatic animals at all sites (range of 0.017–17.534 μg/g ww), as were AHs (range of 0.423–4.549 μg/g ww); the highest levels of PAHs and AHs were found in bivalves from the Mississippi River. When analysis of variance (α = 0.05) was performed with data from aquatic animals, there were only two significant relationships between PAHs, AHs, and OCs