Biogeochemical Mechanisms of Selenium Exchange between Water and Sediments in Two Contrasting Lentic Environments

The biogeochemical mechanisms of Se exchange between water and sediments in two contrasting lentic environments were assessed through examination of Se speciation in the water column, porewater, and sediment. High-resolution (7 mm) vertical profiles of

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Veröffentlicht in:Environmental science & technology 2011-04, Vol.45 (7), p.2605-2612
Hauptverfasser: Martin, Alan J, Simpson, Stephanie, Fawcett, Skya, Wiramanaden, Cheryl I. E, Pickering, Ingrid J, Belzile, Nelson, Chen, Y.-W, London, Jacqueline, Wallschläger, Dirk
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container_issue 7
container_start_page 2605
container_title Environmental science & technology
container_volume 45
creator Martin, Alan J
Simpson, Stephanie
Fawcett, Skya
Wiramanaden, Cheryl I. E
Pickering, Ingrid J
Belzile, Nelson
Chen, Y.-W
London, Jacqueline
Wallschläger, Dirk
description The biogeochemical mechanisms of Se exchange between water and sediments in two contrasting lentic environments were assessed through examination of Se speciation in the water column, porewater, and sediment. High-resolution (7 mm) vertical profiles of
doi_str_mv 10.1021/es103604p
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At both sites Se(VI) is removed from solution in suboxic near-surface porewaters demonstrating that the sediments are serving as diffusive sinks for Se. X-ray absorption near edge spectroscopy (XANES) of sediments suggests that elemental Se and organo-Se represent the dominant sedimentary sinks for dissolved Se. Dissolved Se(IV) and organo-Se are released to porewaters in the near-surface sediments resulting in the diffusive transport of these species into the water column, where between-site differences in the depths of release can be linked to differences in redox zonation. 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High-resolution (7 mm) vertical profiles of &lt;0.45 μm Se species across the sediment-water interface demonstrate that the behavior of dissolved Se(VI), Se(IV), and organo-Se are closely linked to redox conditions as revealed by porewater profiles of redox-sensitive species (dissolved O2, NO3 −, Fe, Mn, SO4 2-, and ΣH2S). At both sites Se(VI) is removed from solution in suboxic near-surface porewaters demonstrating that the sediments are serving as diffusive sinks for Se. X-ray absorption near edge spectroscopy (XANES) of sediments suggests that elemental Se and organo-Se represent the dominant sedimentary sinks for dissolved Se. Dissolved Se(IV) and organo-Se are released to porewaters in the near-surface sediments resulting in the diffusive transport of these species into the water column, where between-site differences in the depths of release can be linked to differences in redox zonation. The presence or absence of emergent vegetation is proposed to present a dominant control on sedimentary redox conditions as well as on the recycling and persistence of reduced Se species in bottom waters.</abstract><cop>Washington, DC</cop><pub>American Chemical Society</pub><pmid>21446766</pmid><doi>10.1021/es103604p</doi><tpages>8</tpages></addata></record>
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source ACS Publications; MEDLINE
subjects Applied sciences
Biogeochemistry
Carbon - analysis
Characterization of Natural and Affected Environments
Ecological and Environmental Phenomena
Environment
Exact sciences and technology
Fresh Water - chemistry
Geologic Sediments - chemistry
Hydrogen-Ion Concentration
Nitrogen - analysis
Oxidation-Reduction
Pollution
Recycling
Sediments
Selenium
Selenium - analysis
Selenium - chemistry
Selenium - metabolism
Spectrum analysis
Vegetation
Water Pollutants, Chemical - analysis
Water Pollutants, Chemical - chemistry
Water Pollutants, Chemical - metabolism
title Biogeochemical Mechanisms of Selenium Exchange between Water and Sediments in Two Contrasting Lentic Environments
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