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Incorporating Both Physical and Kinetic Limitations in Quantifying Dissolved Oxygen Flux to Aquatic Sediments
Authors:Ben L. O’Connor  Miki Hondzo  Judson W. Harvey
Affiliation:1NRC Postdoctoral Associate, U.S. Geological Survey, Mail Stop 430 National Center, Reston, VA 20192; currently, Environmental Science Division, Argonne National Laboratory, EVS/240 9700 S. Cass Ave., Argonne, IL 60439 (corresponding author). E-mail: boconnor@anl.gov
2Professor, Dept. of Civil Engineering, St. Anthony Falls Laboratory, Univ. of Minnesota-Twin Cities, 2 Third Ave. SE, Minneapolis, MN 55414. E-mail: mhondzo@umn.edu
3Hydrologist, U.S. Geological Survey, Mail Stop 430 National Center, Reston, VA 20192. E-mail: jwharvey@usgs.gov.
Abstract:Traditionally, dissolved oxygen (DO) fluxes have been calculated using the thin-film theory with DO microstructure data in systems characterized by fine sediments and low velocities. However, recent experimental evidence of fluctuating DO concentrations near the sediment-water interface suggests that turbulence and coherent motions control the mass transfer, and the surface renewal theory gives a more mechanistic model for quantifying fluxes. Both models involve quantifying the mass transfer coefficient (k) and the relevant concentration difference (ΔC). This study compared several empirical models for quantifying k based on both thin-film and surface renewal theories, as well as presents a new method for quantifying ΔC (dynamic approach) that is consistent with the observed DO concentration fluctuations near the interface. Data were used from a series of flume experiments that includes both physical and kinetic uptake limitations of the flux. Results indicated that methods for quantifying k and ΔC using the surface renewal theory better estimated the DO flux across a range of fluid-flow conditions.
Keywords:Dissolved oxygen  Oxygen demand  Mass transport  Boundary layer flow  Surface waters  Kinetics  Sediment  
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