Water Contamination (water + contamination)

Distribution by Scientific Domains

Kinds of Water Contamination

  • ground water contamination


  • Selected Abstracts


    Somatic mutant frequency at the HPRT locus in children associated with a pediatric cancer cluster linked to exposure to two superfund sites

    ENVIRONMENTAL AND MOLECULAR MUTAGENESIS, Issue 4 2005
    Pamela M. Vacek
    Abstract The somatic mutant frequency (Mf) of the hypoxanthine phosphoribosyl transferase (HPRT) gene has been widely used as a biomarker for the genotoxic effects of exposure but few studies have found an association with environmental exposures. We measured background Mfs in 49 current and former residents of Dover Township, New Jersey, who were exposed during childhood to industrially contaminated drinking water. The exposed subjects were the siblings of children who developed cancer after residing in Dover Township, where the incidence of childhood cancer has been elevated since 1979. Mfs from this exposed group were compared to Mfs in 43 age-matched, presumably unexposed residents of neighboring communities with no known water contamination and no increased cancer incidence. Statistical comparisons were based on the natural logarithm of Mf (lnMF). The mean Mf for the exposed group did not differ significantly from the unexposed group (3.90 × 10,6 vs. 5.06 × 10,6; P = 0.135), but unselected cloning efficiencies were higher in the exposed group (0.55 vs. 0.45; P = 0.005). After adjustment for cloning efficiency, lnMf values were very similar in both groups and age-related increases were comparable to those previously observed in healthy children. The results suggest that HPRT Mf may not be a sensitive biomarker for the genotoxic effects of environmental exposures in children, particularly when substantial time has elapsed since exposure. Environ. Mol. Mutagen., 2005. © 2005 Wiley-Liss, Inc. [source]


    In situ and laboratory bioassays with Chironomus riparius larvae to assess toxicity of metal contamination in rivers: The relative toxic effect of sediment versus water contamination

    ENVIRONMENTAL TOXICOLOGY & CHEMISTRY, Issue 9 2007
    Mafalda S. Faria
    Abstract We used bioassays employing head capsule width and body length increase of Chironomus riparius larvae as end points to evaluate metal contamination in streams. Bioassays were performed in situ near an abandoned Portuguese goldmine in the spring of 2003 and 2004. Bioassays also were performed under laboratory conditions with water and sediment collected from each stream to verify if laboratory bioassays could detect in situ toxicity and to evaluate the relative contribution of sediment and water to overall toxicity. We used field sediments with control water and control sediments with field water to discriminate between metal contamination in water and sediment. Field water with dry and sieved, organic matter,free, and nontreated sediments was used to determine the toxicity of heavy metals that enter the organism through ingested material. In both in situ and laboratory bioassays, body length increase was significantly inhibited by metal contamination, whereas head capsule width was not affected. Body length increase was more affected by contaminated sediment compared to contaminated water. The lowest-effect level of heavy metals was observed in the dry and sieved sediment that prevented ingestion of sediment particles by larvae. These results suggest that body length increase of C. riparius larvae can be used to indicate the impact of metal contamination in rivers. Chironomus riparius larvae are more affected by heavy metals that enter the organism through ingested sediment than by heavy metals dissolved in the water column. Nevertheless, several factors, such as the particle size and organic matter of sediment, must be taken into account. [source]


    Sorption and leaching behaviour of polar aromatic acids in agricultural soils by batch and column leaching tests

    EUROPEAN JOURNAL OF SOIL SCIENCE, Issue 3 2005
    R. Celis
    Summary Aromatic acids can reach the soil from direct anthropogenic activities or, indirectly, from the degradation of many aromatic compounds, such as pesticides or polycyclic aromatic hydrocarbons. Because of the anionic character of aromatic acids at the pH of most soil and sediment environments, they are expected to move rapidly through the soil profile and to pose a great risk of ground water contamination. We designed batch and column leaching tests to characterize the behaviour of three aromatic acids differing in their chemical structures, picloram (4-amino-3,5,6-trichloropicolinic acid), phthalic acid (2,2-benzenedicarboxylic acid), and salicylic acid (2-hydroxybenzoic acid), in four European soils with different physicochemical characteristics. Batch experiments revealed that the persistence of the three acids in soil:water suspensions decreased in the order: picloram , phthalic acid > salicylic acid, and their dissipation curves were relatively independent of soil type. Sorption by the soils, their clay-size fractions and model sorbents indicated much greater affinity of soil constituents for salicylic acid than for picloram or phthalic acid, most likely due to the ability of salicylic acid to form bidentate complexes with positively charged soil components. The extent of leaching of the aromatic acids in hand-packed soil columns decreased in the order: picloram (90,96%) > phthalic acid (25,90%) > salicylic acid (0,37%), which was consistent with the sorption and persistence results of the batch tests. The organic C content, the amount of small-size pores, and the initial concentration of aromatic acid in soil appeared to be important factors influencing the leaching patterns of phthalic acid and salicylic acid in the soils studied, but did not greatly influence the leaching pattern of picloram. Sorption and leaching of polar aromatic acids in soil can therefore vary considerably depending on the structural characteristics of the aromatic acid or soil type. [source]


    Managing Environmental Impacts of Recreation and Tourism in Rainforests of the Wet Tropics of Queensland World Heritage Area

    GEOGRAPHICAL RESEARCH, Issue 2 2005
    Stephen M. Turton
    Abstract This paper describes environmental impacts of tourism and recreation activities in the world heritage listed rainforests of northeast Australia and presents management strategies for sustainable visitor use of the protected area. Tropical rainforests are characterised by their low resistance and moderate to high resilience to impacts associated with human visitation. Visitor use in the World Heritage Area is mostly associated with walking tracks, camping areas, day use areas and off-road vehicle use of old forestry roads and tracks. Adverse environmental impacts range from vegetation trampling, soil compaction, water contamination and soil erosion at the local scale through to spread of weeds, feral animals and soil pathogens along extensive networks of old forestry roads and tracks at the regional scale. Concentration of visitor use is the most desirable management strategy for controlling adverse impacts at most World Heritage Area visitor nodes and sites, and includes methods such as site hardening and shielding to contain impacts. For dispersed visitor activities, such as off-road vehicle driving and long-distance walking, application of best practice methods by the tourist industry and recreational users such as removal of mud and soils from vehicle tyres and hiking boots before entering pathogen-free catchments, together with seasonal closure of roads and tracks, are the preferred management strategies. Retention of canopy cover at camping areas and day use areas, as well as along walking tracks and forestry roads is a simple, yet effective, management strategy for reduction of a range of adverse impacts, including dispersal of weeds and feral animals, edge effects, soil erosion and nutrient loss, road kill and linear barrier effects on rainforest fauna. [source]


    Validation of Numerical Ground Water Models Used to Guide Decision Making

    GROUND WATER, Issue 2 2004
    Ahmed E. Hassan
    Many sites of ground water contamination rely heavily on complex numerical models of flow and transport to develop closure plans. This complexity has created a need for tools and approaches that can build confidence in model predictions and provide evidence that these predictions are sufficient for decision making. Confidence building is a long-term, iterative process and the author believes that this process should be termed model validation. Model validation is a process, not an end result. That is, the process of model validation cannot ensure acceptable prediction or quality of the model. Rather, it provides an important safeguard against faulty models or inadequately developed and tested models. If model results become the basis for decision making, then the validation process provides evidence that the model is valid for making decisions (not necessarily a true representation of reality). Validation, verification, and confirmation are concepts associated with ground water numerical models that not only do not represent established and generally accepted practices, but there is not even widespread agreement on the meaning of the terms as applied to models. This paper presents a review of model validation studies that pertain to ground water flow and transport modeling. Definitions, literature debates, previously proposed validation strategies, and conferences and symposia that focused on subsurface model validation are reviewed and discussed. The review is general and focuses on site-specific, predictive ground water models used for making decisions regarding remediation activities and site closure. The aim is to provide a reasonable starting point for hydrogeologists facing model validation for ground water systems, thus saving a significant amount of time, effort, and cost. This review is also aimed at reviving the issue of model validation in the hydrogeologic community and stimulating the thinking of researchers and practitioners to develop practical and efficient tools for evaluating and refining ground water predictive models. [source]


    Ground Water Chlorinated Ethenes in Tree Trunks: Case Studies, Influence of Recharge, and Potential Degradation Mechanism

    GROUND WATER MONITORING & REMEDIATION, Issue 3 2004
    Don A. Vroblesky
    Trichloroethene (TCE) was detected in cores of trees growing above TCE-contaminated ground at three sites: the Carswell Golf Course in Texas, Air Force Plant PJKS in Colorado, and Naval Weapons Station Charleston in South Carolina. This was true even when the depth to water was 7.9 m or when the contaminated aquifer was confined beneath ,3 m of clay. Additional ground water contaminants detected in the tree cores were cis,1,2-dichloroethene at two sites and tetrachloroethene at one site. Thus, tree coring can be a rapid and effective means of locating shallow subsurface chlorinated ethenes and possibly identifying zones of active TCE dechlorination. Tree cores collected over time were useful in identifying the onset of ground water contamination. Several factors affecting chlorinated ethene concentrations in tree cores were identified in this investigation. The factors include ground water chlorinated ethene concentrations and depth to ground water contamination. In addition, differing TCE concentrations around the trunk of some trees appear to be related to the roots deriving water from differing areas. Opportunistic uptake of infiltrating rainfall can dilute prerain TCE concentrations in the trunk. TCE concentrations in core headspace may differ among some tree species. In some trees, infestation of bacteria in decaying heartwood may provide a TCE dechlorination mechanism within the trunk. [source]


    Used Motor Oil as a Source of MTBE, TAME, and BTEX to Ground Water

    GROUND WATER MONITORING & REMEDIATION, Issue 4 2002
    Ronald J. Baker
    Methyl tert-butyl ether (MTBE), the widely used gasoline oxygenate, has been identified as a common ground water contaminant, and BTEX compounds (benzene, toluene, ethylbenzene, and xylenes) have long been associated with gasoline spills. Because not all instances of ground water contamination by MTBE and BTEX can be attributed to spills or leaking storage tanks, other potential sources need to be considered. In this study, used motor oil was investigated as a potential source of these contaminants. MTBE in oil was measured directly by methanol extraction and gas chromatography using a flame ionization detector (GC/FID). Water was equilibrated with oil samples and analyzed for MTBE, BTEX, and the oxygenate tert-amyl methyl ether (TAME) by purge- and-trap concentration followed by GC/FID analysis. Raoult's law was used to calculate oil-phase concentrations of MTBE, BTEX, and TAME from aqueous-phase concentrations. MTBE, TAME, and BTEX were not detected in any of five new motor oil samples, whereas these compounds were found at significant concentrations in all six samples of the used motor oil tested for MTBE and all four samples tested for TAME and BTEX. MTBE concentrations in used motor oil were on the order of 100 mg/L. TAME concentrations ranged from 2.2 to 87 mg/L. Concentrations of benzene were 29 to 66 mg/L, but those of other BTEX compounds were higher, typically 500 to 2000 mg/L. [source]


    Use of models to assess the reduction in contamination of water bodies by agricultural pesticides through the implementation of policy instruments: a case study of the Voluntary Initiative in the UK

    PEST MANAGEMENT SCIENCE (FORMERLY: PESTICIDE SCIENCE), Issue 12 2006
    James Garratt
    Abstract Through normal agricultural use, pesticides may reach environmental water bodies via several routes of entry. Various policies and initiatives exist to reduce the effects of pesticides in the environment. One such initiative in place in the UK is the Voluntary Initiative (VI). The VI is a voluntary scheme put forward by the Crop Protection Association with other crop protection and farming organisations to reduce the environmental impacts of pesticides. Mathematical models of pesticide fate can usefully be applied to examine the impact of factors influencing the contamination of water bodies by pesticides. The work reported here used water quality models to examine how changes in farmer behaviour could potentially impact pesticide contamination of environmental water bodies. As far as possible, uncalibrated, standard regulatory models were used. Where suitable models were not available, simple models were defined for the purposes of the study and calibrated using literature data. Scenarios were developed to represent different standards of practice with respect to pesticide user behaviour. The development of these scenarios was guided by the Crop Protection Management Plan (CPMP) aspect of the VI. A framework for the use of modelling in the evaluation of the VI is proposed. The results of the modelling study suggest that, in several areas, widespread adoption of the measures proposed in the VI could lead to reductions in pesticide contamination of environmental water bodies. These areas include pesticide contamination from farmyards, spray drift and field runoff. In other areas (including pesticide leaching to groundwater and contamination of surface water from field drains) the benefits that may potentially be gained from the VI are less clear. A framework to evaluate the VI should take into consideration the following aspects: (1) groundwater is more at risk when there is a combination of leachable compounds, vulnerable soils, shallow groundwater and high product usage; (2) surface water contamination from drains is most likely when heavy rain falls soon after application, the soils are vulnerable and product usage is high; (3) surface water contamination from drift is most likely when the distance between the spray boom and water body is small and product usage is high; (4) surface water contamination from farmyards is dependent on the nature of the farmyard surface, the competence of the spray operator and the level of product usage. Any policy or initiative to reduce pesticide contamination should be measured against farmer behaviour in these areas. © Crown copyright 2006. Reproduced with the permission of Her Majesty's Stationery Office. Published by John Wiley & Sons, Ltd. [source]


    Methodology and model for performance and cost comparison of innovative treatment technologies at wood preserving sites

    REMEDIATION, Issue 1 2001
    Mark L. Evans
    Wood preserving facilities have used a variety of compounds, including pentachlorophenol (PCP), creosote, and certain metals, to extend the useful life of wood products. Past operations and waste management practices resulted in soil and water contamination at a portion of the more than 700 wood preserving sites in the United States (EPA, 1997). Many of these sites are currently being addressed under federal, state, or voluntary cleanup programs. The U.S. Environmental Protection Agency (EPA) National Risk Management Research Laboratory (NRMRL) has responded to the need for information aimed at facilitating remediation of wood preserving sites by conducting treatability studies, issuing guidance, and preparing reports. This article presents a practical methodology and computer model for screening the performances and comparing the costs of seven innovative technologies that could be used for the treatment of contaminated soils at user-specified wood preserving sites. The model incorporates a technology screening function and a cost-estimating function developed from literature searches and vendor information solicited for this study. This article also provides background information on the derivation of various assumptions and default values used in the model, common contaminants at wood preserving sites, and recent trends in the cleanup of such sites. © 2001 John Wiley & Sons, Inc. [source]


    Sequestration of Heavy Metals from Water with Layered Metal Sulfides

    CHEMISTRY - A EUROPEAN JOURNAL, Issue 19 2009
    Manolis
    Abstract Extraordinarily effective heavy metal ion scavenger: We show here that the material K2xMnxSn3,xS6 (x=0.5,0.95) (KMS-1) overcomes the limitations of the known heavy metal ion sorbents, showing the capability to rapidly reduce the concentrations of Cd, Hg, and Pb ions well-below the legally acceptable levels for drinking water. KMS-1 is inexpensive, easily prepared in large quantities, and may play a role in addressing the global problem of water contamination with heavy metal ions. The paradigm of heavy metal ion absorption of KMS-1 is the ability to form very strong MS bonds. [source]