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  • 1
    Call number: SR 90.0002(1404-E)
    In: Professional paper
    Type of Medium: Series available for loan
    Pages: VI, E-45 S. + 2 pl.
    Series Statement: U.S. Geological Survey professional paper 1404-E
    Language: English
    Location: Lower compact magazine
    Branch Library: GFZ Library
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  • 2
    Call number: SR 90.0004(2399)
    In: United States Geological Survey water-supply paper
    Type of Medium: Series available for loan
    Pages: VII, 95 S.
    Series Statement: U.S. Geological Survey water-supply paper 2399
    Language: English
    Location: Lower compact magazine
    Branch Library: GFZ Library
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  • 3
    Call number: SR 90.0002(1404-J)
    In: Professional paper
    Type of Medium: Series available for loan
    Pages: X, J-41 S. + 9 pl.
    Series Statement: U.S. Geological Survey professional paper 1404-J
    Language: English
    Location: Lower compact magazine
    Branch Library: GFZ Library
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  • 4
    ISSN: 1745-6584
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Energy, Environment Protection, Nuclear Power Engineering , Geosciences
    Notes: Total concentrations of formate, acetate, and isobutyrate varied from less than 5 to greater than 9,000 μmol/l over distances of 〈 3 m in ground water from a shallow hydrocarbon contaminated aquifer. Laboratory incubations of aquifer material indicate that organic acid concentrations were dependent on the amount of hydrocarbon loading in the sediment and the relative rates of microbial organic acid production and consumption. In heavily contaminated sediments, production greatly exceeded consumption and organic acid concentrations increased. In lightly contaminated sediments rates were essentially equal and organic acid concentrations remained low. Concentrations of dissolved calcium, magnesium, and iron generally were one to two orders of magnitude higher in organic acid-rich ground water than in ground water having low organic acid concentrations. Carbonate and Fe(III)-oxyhydroxide minerals were the likely sources of these elements. Similarly, concentrations of dissolved silica, derived from quartz and k-feldspar, were higher in organic acid-rich ground water than in other waters. The positive relation (r = 0.60, p 〈 .05, n = 16) between concentrations of silica and organic acids suggests that the microbially mediated buildup of organic acids in ground water enhanced quartz/k-feldspar dissolution in the aquifer, although it was not the only factor influencing their dissolution. A model that included organic acid microequivalents normalized by cation microequivalents significantly strengthened the correlation (r = 0.79, p 〈 .001, n = 16) between dissolved silica and organic acid concentrations, indicating that competition between silica and cations for complexation sites on organic acids also influenced quartz/k-feldspar dissolution. Physical evidence for enhanced mineral dissolution in organic acid-rich waters included scanning electron microscopy images of highly corroded quartz and k-feldspar grains from portions of the aquifer containing organic acid-rich ground water. Microporosity generated in hydrocarbon contaminated sediments may adversely affect remediation efforts that depend on the efficient injection of electron acceptors into an aquifer or on the recovery of solutes from an aquifer.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Ground water 29 (1991), S. 0 
    ISSN: 1745-6584
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Energy, Environment Protection, Nuclear Power Engineering , Geosciences
    Notes: Decomposition of organic-rich bottom sediment in a tidal creek in Maryland results in production of gas bubbles in the bottom sediment during summer and fall. In areas where volatile organic contaminants discharge from ground water, through the bottom sediment, and into the creek, part of the volatile contamination diffuses into the gas bubbles and is released to the atmosphere by ebullition. Collection and analysis of gas bubbles for their volatile organic contaminant content indicate that relative concentrations of the volatile organic contaminants in the gas bubbles are substantially higher in areas where the same contaminants occur in the ground water that discharges to the streams. Analyses of the bubbles located an area of previously unknown ground-water contamination.The method developed for this study consisted of disturbing the bottom sediment to release gas bubbles, and then capturing the bubbles in a polyethylene bag at the water-column surface. The captured gas was transferred either into sealable polyethylene bags for immediate analysis with a photoionization detector or by syringe to glass tubes containing wires coated with an activated-carbon adsorbent. Relative concentrations were determined by mass spectral analysis for chloroform and trichloroethylene.
    Type of Medium: Electronic Resource
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  • 6
    ISSN: 1745-6584
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Energy, Environment Protection, Nuclear Power Engineering , Geosciences
    Notes: Forty passive vapor samplers were placed in creek-bottom sediment in an area where ground water contaminated with volatile organic compounds is discharging to surface water. The vapor samplers were composed of activated carbon fused to a ferromagnetic wire in a test tube. The samplers were analyzed in a laboratory using an extranuclear quadrupole mass spectrometer. Data from the samplers reveal distributions of chloroform, tetrachloroethylene, trichloroethylene, and benzene in the bottom sediment that closely correspond to the distribution of those compounds in the adjacent ground water. Moreover, concentrations of tetrachloroethylene in bottom sediment estimated from the samplers are similar to those measured in observation wells near the shoreline. Thus, the passive vapor samplers may be used to locate and map areas where contaminated ground water is being discharged to surface water and to determine the approximate concentrations of specific contaminants in the discharging ground water.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Ground water 28 (1990), S. 0 
    ISSN: 1745-6584
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Energy, Environment Protection, Nuclear Power Engineering , Geosciences
    Notes: The annual growth rings of tulip trees (Liriodendron tulipifera L.) appear to preserve a chemical record of ground-water contamination at a landfill in Maryland. Zones of elevated iron and chlorine concentrations in growth rings from trees immediately downgradient from the landfill are closely correlated temporally with activities in the landfill expected to generate iron and chloride contamination in the ground water. Successively later iron peaks in trees increasingly distant from the landfill along the general direction of ground-water flow imply movement of iron-contaminated ground water away from the landfill. The historical velocity of iron movement (2 to 9 m/yr) and chloride movement (at least 40 m/yr) in ground water at the site was estimated from element-concentration trends of trees at successive distances from the landfill. The tree-ring-derived chloride-transport velocity approximates the known ground-water velocity (30 to 80 m/yr). A minimum horizontal hydraulic conductivity (0.01 to .02 cm/s) calculated from chloride velocity agrees well with values derived from aquifer tests (about 0.07 cm/s) and from ground-water modeling results (0.009 to 0.04 cm/s).
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Ground water 43 (2005), S. 0 
    ISSN: 1745-6584
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Energy, Environment Protection, Nuclear Power Engineering , Geosciences
    Type of Medium: Electronic Resource
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  • 9
    ISSN: 1745-6584
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Energy, Environment Protection, Nuclear Power Engineering , Geosciences
    Notes: Rates of biodegradation were measured in a petroleum hydrocarbon-contaminated aquifer using a combination of field and laboratory methods. These methods are based on tracking concentration changes of substrates (both electron donors and acceptors) or final products of microbial metabolism over time. Ground water at the study site (Hanahan, South Carolina) is anoxic, and sulfate reduction is the predominant terminal electron accepting process. Laboratory studies conducted with sediment cored from the site showed that 14C-toluene was mineralized to 14CO2 with a first-order degradation rate constant (ktol) of -0.01 d−1 under sulfate-reducing conditions. Under nitrate-amended, Fe(III)-amended, or nonamended (methanogenic) conditions, toluene was not significantly mineralized. 14C-Benzene was degraded at low but measurable rates (kben= -0.003 d−1) under sulfate-reducing conditions whereas degradation under methanogenic conditions was negligible. These results illustrate the extreme sensitivity of laboratory-measured biodegradation rates to terminal electron-accepting conditions, and show the necessity of carefully matching experimental conditions to in situ conditions. Concentration decreases of toluene along aquifer flowpaths, when the uncertainty of ground-water flow velocities was considered, indicated ktol values ranging from -0.0075 to -0.03 d−1. Concentration decreases of sulfate and concentration increases of dissolved inorganic carbon (DIC), when normalized for assumed stoichiometric oxidation of toluene coupled to sulfate reduction, yielded a kso4 range of -0.005 to -0.02 d−1, and a kDIC value range of +0.00075 to +0.003 d−1. Because both laboratory and field methods have numerous sources of uncertainty, a combination of these methods is the most appropriate procedure for evaluating biodegradation rate constants in contaminated ground-water systems.
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Ground water 30 (1992), S. 0 
    ISSN: 1745-6584
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Energy, Environment Protection, Nuclear Power Engineering , Geosciences
    Notes: In 1975, the loss of approximately 83,000 gallons of JP-4 grade jet fuel resulted in contamination of the shallow aquifer near North Charleston, South Carolina. To identify those factors likely to influence microbial activity under denitrifying conditions, we examined the fate of amended NO3, the effect of pH, NO3, and PO4 on denitrification, and the variability of denitrification in sediments collected at the site. Denitrification (N2O-N production) accounted for 98% of the depletion of NO3-N under anaerobic conditions. Both carbon mineralization and denitrification rates increased asymptotically with increasing NO3 to a maximum at approximately 1 mM NO3. Addition of up to 1 mM PO4 did not significantly increase N2O and CO2 production. Denitrification rates were at least 38% lower at pH = 4 than observed at pH = 7. Comparison of samples with differing degrees of hydrocarbon contamination indicated that at least a tenfold variation in sediment denitrification occurs at the North Charleston site.
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