Browsing by Author "Vengosh, A"
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Item Open Access Climate change, water resources, and the politics of adaptation in the Middle East and North Africa(Climatic Change, 2011-02-01) Sowers, J; Vengosh, A; Weinthal, EThrough an examination of global climate change models combined with hydrological data on deteriorating water quality in the Middle East and North Africa (MENA), we elucidate the ways in which the MENA countries are vulnerable to climate-induced impacts on water resources. Adaptive governance strategies, however, remain a low priority for political leaderships in the MENA region. To date, most MENA governments have concentrated the bulk of their resources on large-scale supply side projects such as desalination, dam construction, inter-basin water transfers, tapping fossil groundwater aquifers, and importing virtual water. Because managing water demand, improving the efficiency of water use, and promoting conservation will be key ingredients in responding to climate-induced impacts on the water sector, we analyze the political, economic, and institutional drivers that have shaped governance responses. While the scholarly literature emphasizes the importance of social capital to adaptive governance, we find that many political leaders and water experts in the MENA rarely engage societal actors in considering water risks. We conclude that the key capacities for adaptive governance to water scarcity in MENA are underdeveloped. © 2010 Springer Science+Business Media B.V.Item Open Access Environmental Impacts of the Coal Ash Spill in Kingston, Tennessee: An 18-Month Survey(2010) Ruhl; L; Vengosh, A; Dwyer; G, S; Hsu-Kim; H; DeonarineAn 18 month investigation of the environmental impacts of the Tennessee Valley Authority (TVA) coal ash spill in Kingston, Tennessee combined with leaching experiments on the spilled TVA coal ash have revealed that leachable coal ash contaminants (LCACs), particularly arsenic, selenium, boron, strontium, and barium, have different effects on the quality of impacted environments. While LCACs levels in the downstream river water are relatively low and below the EPA drinking water and ecological thresholds, elevated levels were found in surface water with restricted water exchange and in pore water extracted from the river sediments downstream from the spill. The high concentration of arsenic (up to 2000 mu g/L) is associated with some degree of anoxic conditions and predominance of the reduced arsenic species (arsenite) in the pore waters. Laboratory leaching simulations show that the pH and ash/water ratio control the LCACs' abundance and geochemical composition of the impacted water. These results have important implications for the prediction of the fate and migration of LCACs in the environment, particularly for the storage of coal combustion residues (CCRs) in holding ponds and landfills, and any potential CCRs effluents leakage into lakes, rivers, and other aquatic systems.Item Open Access Evaluating salinity sources of groundwater and implications for sustainable reverse osmosis desalination in coastal North Carolina, USA(Hydrogeology Journal, 2011-08-01) Vengosh, A; Vinson, David S; Schwartz, Haylee G; Dwyer, Gary SThe natural and pumping-induced controls on groundwater salinization in the coastal aquifers of North Carolina, USA, and the implications for the performance of a reverse osmosis (RO) desalination plant have been investigated. Since installation of the well field in the Yorktown aquifer in Kill Devil Hills of Dare County during the late 1980s, the groundwater level has declined and salinity of groundwater has increased from ∼1,000 to ∼2,500 mg/L. Geochemical and boron isotope analyses suggest that the salinity increase is derived from an upflow of underlying saline groundwater and not from modern seawater intrusion. In the groundwater of four wells supplying the plant, elevated boron and arsenic concentrations were observed (1.3–1.4 mg/L and 8–53 μg/L, respectively). Major ions are effectively rejected by the RO membrane (96–99% removal), while boron and arsenic are not removed as effectively (16–42% and 54–75%, respectively). In coming decades, the expected rise of salinity will be associated with higher boron content in the groundwater and consequently also in the RO-produced water. In contrast, there is no expectation of an increase in the arsenic content of the salinized groundwater due to the lack of increase of arsenic with depth and salinity in Yorktown aquifer groundwater.Item Open Access Origin of Hexavalent Chromium in Drinking Water Wells from the Piedmont Aquifers of North Carolina(Environmental Science and Technology Letters, 2016-12-13) Vengosh, A; Coyte, R; Karr, J; Harkness, JS; Kondash, AJ; Ruhl, LS; Merola, RB; Dywer, GSHexavalent chromium [Cr(VI)] is a known pulmonary carcinogen. Recent detection of Cr(VI) in drinking water wells in North Carolina has raised public concern about contamination of drinking water wells by nearby coal ash ponds. Here we report, for the first time, the prevalence of Cr and Cr(VI) in drinking water wells from the Piedmont region of central North Carolina, combined with a geochemical analysis to determine the source of the elevated Cr(VI) levels. We show that Cr(VI) is the predominant species of dissolved Cr in groundwater and elevated levels of Cr and Cr(VI) are found in wells located both near and far ( > 30 km) from coal ash ponds. The geochemical characteristics, including the overall chemistry, boron to chromium ratios, and strontium isotope ( 87 Sr/ 86 Sr) variations in groundwater with elevated Cr(IV) levels, are different from those of coal ash leachates. Alternatively, the groundwater chemistry and Sr isotope variations are consistent with water-rock interactions as the major source for Cr(VI) in groundwater. Our results indicate that Cr(VI) is most likely naturally occurring and ubiquitous in groundwater from the Piedmont region in the eastern United States, which could pose health risks to residents in the region who consume well water as a major drinking water source.Item Open Access Relationships between radium and radon occurrence and hydrochemistry in fresh groundwater from fractured crystalline rocks, North Carolina (USA)(Chemical Geology, 2009-03-30) Vinson, DS; Vengosh, A; Hirschfeld, D; Dwyer, GSNaturally-occurring radionuclides (uranium, radium, and radon), major dissolved constituents, and trace elements were investigated in fresh groundwater in 117 wells in fractured crystalline rocks from the Piedmont region (North Carolina, USA). Chemical variations show a general transition between two water types: (1) slightly acidic (pH 5.0-6.0), oxic, low-total dissolved solids (TDS) waters, and (2) near neutral, oxic to anoxic, higher-TDS waters. The uranium, radium, and radon levels in groundwater associated with granite (Rolesville Granite) are systematically higher than other rock types (gneiss, metasedimentary, and metavolcanic rocks). Water chemistry plays a secondary role on radium and radon distributions as the 222Rn/226Ra activity ratio is correlated with redox-sensitive solutes such as dissolved oxygen and Mn concentrations, as well as overall dissolved solids content including major divalent cations and Ba. Since 224Ra/228Ra activity ratios in groundwater are close to 1, we suggest that mobilization of Ra and Rn is controlled by alpha recoil processes from parent nuclides on fracture surfaces, ruling out Ra sources from mineral dissolution or significant long-distance Ra transport. Alpha recoil is balanced by Ra adsorption that is influenced by redox conditions and/or ion concentrations, resulting in an approximately one order of magnitude decrease (~ 20,000 to ~ 2000) in the apparent Ra distribution coefficient between oxygen-saturated and anoxic conditions and also across the range of dissolved ion concentrations (up to ~ 7 mM). Thus, the U and Th content of rocks is the primary control on observed Ra and Rn activities in groundwater in fractured crystalline rocks, and in addition, linked dissolved solids concentrations and redox conditions impart a secondary control. © 2008 Elsevier B.V. All rights reserved.Item Open Access Survey of the potential environmental and health impacts in the immediate aftermath of the coal ash spill in Kingston, Tennessee.(Environ Sci Technol, 2009-08-15) Ruhl, L; Vengosh, A; Dwyer, GS; Hsu Kim, H; Deonarine, A; Bergin, M; Kravchenko, JAn investigation of the potential environmental and health impacts in the immediate aftermath of one of the largest coal ash spills in U.S. history at the Tennessee Valley Authority (TVA) Kingston coal-burning power plant has revealed three major findings. First the surface release of coal ash with high levels of toxic elements (As = 75 mg/kg; Hg = 150 microg/kg) and radioactivity (226Ra + 228Ra = 8 pCi/g) to the environment has the potential to generate resuspended ambient fine particles (< 10 microm) containing these toxics into the atmosphere that may pose a health risk to local communities. Second, leaching of contaminants from the coal ash caused contamination of surface waters in areas of restricted water exchange, but only trace levels were found in the downstream Emory and Clinch Rivers due to river dilution. Third, the accumulation of Hg- and As-rich coal ash in river sediments has the potential to have an impact on the ecological system in the downstream rivers by fish poisoning and methylmercury formation in anaerobic river sediments.Item Open Access The Global Biogeochemical Cycle of Arsenic(Global Biogeochemical Cycles, 2022-11-01) Schlesinger, WH; Klein, EM; Vengosh, ADirect exploitation and use of arsenic resources has diminished in recent years, but inadvertent mobilizations of As from mineral extractions (metal ores, coal, and phosphate rock) are now as much as ten-fold greater (1,500–5,600 × 109 g/yr) than the As released by the natural rate of rock weathering at the Earth's surface (60–544 × 109 g/yr). Although some As from mining activities enters global cycling through leaching and spills, the amount of dissolved As in rivers (23 × 109 g/yr) is similar to the theoretical mobilization of As from chemical weathering. Anthropogenic emissions to the atmosphere (17–38 × 109 g As/yr) are double the natural background sources (10–25 × 109 g As/yr), largely as a result of the smelting of Cu and other non-ferrous ores. This results in increased atmospheric deposition near regions with high mining and industrial activities, with potential consequences to human health, natural ecosystems and agriculture. Using median values for As, the ratio of anthropogenic to natural emissions to the atmosphere (1.57) suggests a human impact on the global As cycle that rivals those for V, Hg and Pb.Item Open Access Water quality implications of the neutralization of acid mine drainage with coal fly ash from India and the United States(Fuel, 2022-12-15) Weinberg, R; Coyte, R; Wang, Z; Das, D; Vengosh, ASubsurface coal mining often induces the formation of acid mine drainage (AMD) in active and abandoned coal mines while coal combustion generates coal combustion residuals (CCR), including fly ash (FA), with elevated levels of toxic metals. Decades of AMD and CCR production have caused major environmental and human health impacts. Given the typically elevated level of oxides in FA, previous studies have examined its potential to neutralize AMD and remove the associated metals. While the neutralization of AMD through reaction with FA has been demonstrated to successfully remove cationic metals, the fate of oxyanion forming elements are less well studied and is the focus of this study. Here we conducted 49 different experiments in which simulated AMD solutions were interacted with representative U.S. (n = 7) and Indian (n = 6) FA samples through controlled liquid to solid ratios in short-term (24 h) and long-term (up to 5 weeks) lab-scale experiments. We show that Class-F FA, originating from Gondwana and Northeastern Tertiary coals in India, has limited neutralization capacity, while Class-C FA, with high CaO and MgO contents from Powder River coals in the U.S. has the greatest AMD neutralization capacity among the studied fly ashes. The neutralization experiments show that AMD-FA reactions cause the removal of cationic elements (i.e., Fe, Mn, and Al) from solution, while at the same time, leaching oxyanion forming elements (i.e., As, Se, Mo, Cr, B, Tl, and Sb) from the FA, increasing the potential environmental risks from the treated leachates. The magnitude of mobilization of these elements depends on their concentrations in the FA and the pH conditions. We show that using FA from the Appalachian and Illinois coals efficiently neutralizes AMD, but also results in secondary contamination of the treated effluents with oxyanion forming elements to levels exceeding drinking water and ecological standards, which could contaminate the ambient environment, whereas neuralization with Powder River Basin Class-C FA induces only limited contamination.