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Combined use of 15N and 18O of nitrate and 11B to evaluate nitrate contamination in groundwater
Institution:1. School of Earth and Environmental Sciences (BK21 SEES), Seoul National University, Seoul 151–747, South Korea;2. Department of Geoscience, University of Calgary, 2500 University Drive NW, Calgary T2N 1N4, Alberta, Canada;3. Department of Geology, Kangwon National University, Chuncheon 200–701, South Korea;4. Planning and Management Group, Korea Environment Institute, Sejong 339-007, South Korea;1. BRGM, Avenue C. Guillemin, BP 36009, 45060 Orléans Cedex 02, France;2. BRGM, Réunion Agency, 5, rue Sainte-Anne, CS 51016, 97404 Saint Denis Cedex, France;3. BRGM Montpellier Agency, 1039, rue de Pinville, 34000 Montpellier, France;4. Géosciences Montpellier, UMR 5243, Université de Montpellier, cc069, Place Eugène Bataillon, 34095 Montpellier Cedex 05, France
Abstract:Isotopic composition of NO3 (δ15NNO3 and δ18ONO3) and B (δ11B) were used to evaluate NO3 contamination and identify geochemical processes occurring in a hydrologically complex Basin and Range valley in northern Nevada with multiple potential sources of NO3. Combined use of these isotopes may be a useful tool in identifying NO3 sources because NO3 and B co-migrate in many environmental settings, their isotopes are fractionated by different environmental processes, and because wastewater and fertilizers may have distinct isotopic signatures for N and B. The principal cause of elevated NO3 concentrations in residential parts of the study area is wastewater and not natural NO3 or fertilizers. This is indicated by some samples with elevated NO3 concentrations plotting along δ15NNO3 and NO3 mixing lines between natural NO3 from the study area and theoretical septic-system effluent. This conclusion is supported by the presence of caffeine in one sample and the absence of samples with elevated NO3 concentrations that fall along mixing lines between natural NO3 and theoretical percolate below fertilized lawns. Nitrogen isotopes alone could not be used to determine NO3 sources in several wells because denitrification blurred the original isotopic signatures. The range of δ11B values in native ground water in the study area (?8.2‰ to +21.2‰) is large. The samples with the low δ11B values have a geochemical signature characteristic of hydrothermal systems. Physical and chemical data suggest B is not being strongly fractionated by adsorption onto clays. δ11B values from local STP effluent (?2.7‰) and wash water from a domestic washing machine (?5.7‰) were used to plot mixing lines between wastewater and native ground water. In general, wells with elevated NO3 concentrations fell along mixing lines between wastewater and background water on plots of δ11B against 1/B and Cl/B. Combined use of δ15N and δ11B in the study area was generally successful in identifying contaminant sources and processes that are occurring, however, it is likely to be more successful in simpler settings with a well-characterized δ11B value for background wells.
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