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This article in JEQ

  1. Vol. 31 No. 1, p. 331-338
     
    Received: Dec 27, 2000


    * Corresponding author(s): doner@nature.berkeley.edu
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doi:10.2134/jeq2002.3310

Trace Element Retention and Release on Minerals and Soil in a Constructed Wetland

  1. Patricia M. Fox and
  2. Harvey E. Doner *
  1. Division of Ecosystem Sciences, Department of Environmental Science, Policy, and Management, 151 Hilgard Hall, Univ. of California, Berkeley, CA 94720-3110

Abstract

Constructed wetlands are one method under investigation for the remediation of trace element–contaminated agricultural drainwater. A greater understanding of the retention of trace elements by the bulk soil and soil constituents is necessary for their safe and effective use. To determine the capacity of soil, calcite, and goethite-coated quartz sand for retention of As, Mo, and V under field conditions, an in situ method was used whereby permeable bags containing those minerals were placed near the sediment surface of a flow-through constructed wetland for 3 or 12 mo. Accumulations of As, Mo, and V occurred on goethite-coated sand. Concentrations of Mo on goethite-coated sand were much higher in samples from a wetland cell with a water depth of 15 cm (38.23 ± 7.27 mg kg−1) compared with those from a cell with a water depth of 3 cm (8.30 ± 1.45 mg kg−1). Calcite sorbed no As and low amounts of Mo and V, indicating that it is not an important sink for those elements under these conditions. In soil bags, total As and V concentrations showed little change over 12 mo. Molybdenum accumulated in the soil bags, resulting in total concentrations (12 mo) of 27.22 ± 2.69 mg kg−1 and 11.42 ± 1.35 mg kg−1 at water depths of 15 and 3 cm, respectively. Nearly half of the Mo accumulation on soil became water soluble after air-drying. This has important implications for systems that may undergo changes in redox status, possibly resulting in large fluxes of water-soluble Mo.

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Copyright © 2002. American Society of Agronomy, Crop Science Society of America, Soil Science SocietyPublished in J. Environ. Qual.31:331–338.