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Spatial and Temporal Migration of a Landfill Leachate Plume in Alluvium
2015
Masoner, Jason R. | Cozzarelli, Isabelle M.
Leachate from unlined or leaky landfills can create groundwater contaminant plumes that last decades to centuries. Understanding the dynamics of leachate movement in space and time is essential for monitoring, planning and management, and assessment of risk to groundwater and surface-water resources. Over a 23.4-year period (1986–2010), the spatial extent of the Norman Landfill leachate plume increased at a rate of 7800 m²/year and expanded by 878 %, from an area of 20,800 m²in 1986 to 203,400 m²in 2010. A linear plume velocity of 40.2 m/year was calculated that compared favorably to a groundwater-seepage velocity of 55.2 m/year. Plume-scale hydraulic conductivity values representative of actual hydrogeological conditions in the alluvium ranged from 7.0 × 10⁻⁵to 7.5 × 10⁻⁴ m/s, with a median of 2.0 × 10⁻⁴ m/s. Analyses of field-measured and calculated plume-scale hydraulic conductivity distributions indicate that the upper percentiles of field-measured values should be considered to assess rates of plume-scale migration, spreading, and biodegradation. A pattern of increasing Cl⁻concentrations during dry periods and decreasing Cl⁻concentrations during wet periods was observed in groundwater beneath the landfill. The opposite occurred in groundwater downgradient from the landfill; that is, Cl⁻concentrations in groundwater downgradient from the landfill decreased during dry periods and increased during wet periods. This pattern of changing Cl⁻concentrations in response to wet and dry periods indicates that the landfill retains or absorbs leachate during dry periods and produces lower concentrated leachate downgradient. During wet periods, the landfill receives more recharge which dilutes leachate in the landfill but increases leachate migration from the landfill and produces a more concentrated contaminant plume. This approach of quantifying plume expansion, migration, and concentration during variable hydrologic conditions provides increased understanding of plume behavior and migration potential and may be applied at less monitored landfill sites to evaluate potential risks of contamination to downgradient receptors.
Показать больше [+] Меньше [-]Microscale distribution and elemental associations of Se in seleniferous soils in Punjab, India
2015
Eiche, Elisabeth
Several regions around the globe are known to have soils highly enriched in Se. Usually, bulk samples are analysed when characterizing enrichment and mobility of Se in seleniferous soils. In this study, Se concentration and distribution were determined along with other elements on a microscale level in seleniferous soils from Punjab, India, using synchrotron-based X-ray fluorescence (XRF) analysis. Additionally, the mineralogical and geochemical composition of bulk soil material was investigated. Sequential extractions were carried out to gain further insight into preferential Se associations. The objective of this study was to investigate the microscale geochemistry of seleniferous soils in order to be able to deduce information about Se host phases, to characterize the distribution, extent and origin of Se enrichment and to possibly reveal the relevant enrichment processes. Selenium concentrations in the soils vary considerably within tens of micrometers. Thirty times the bulk concentration, the highest Se enrichment was found to be 350 mg/kg. Results show that the primary origin of Se in these soils is probably not from weathering of bedrock or alluvium but rather from an external Se source, like Se-rich irrigation water. Secondary processes like in situ formation of mineral phases, adsorption or transformation to organic species finally lead to an immobilization and fixation of Se in the soils. In this context, reduction of Se oxyanions to elemental Se or to selenide as part of sulfides probably leads to the highest Se enrichment which, however, is mainly spatially confined. Lower Se enrichments are indicated to be due to (co-)precipitation with or adsorption to calcite. Therefore, this extremely heterogeneous distribution of Se must be controlled by small-scale differences in redox and solution chemistry which can develop in small soil structure like micropores or soil aggregates.
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