Metal Bioavailability and Speciation in a Wetland Tailings Repository Amended with Biosolids Compost, Wood Ash, and Sulfate
Pam S. DeVoldera,
Sally L. Brown*,a,
Dean Hesterbergc and
Kumi Pandyab
a College of Forest Resources, Box 352100, Univ. of Washington, Seattle, WA 98195-2100
b National Synchrotron Light Source, Brookhaven National Laboratory, Upton, NY 11973
c Dep. of Soil Science, Box 7619, North Carolina State Univ., Raleigh, NC 27695-7619

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Fig. 1. A diagram of the experimental units used for the study. The diagram shows the depth of the tailings, compost amendment, and water cover. It also shows the amendment, interface, and tailings sampling points.
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Fig. 2. Sediment redox potential (Eh) values averaged over all replicates of the north plot (NP) and south plot (SP) sediments for each sampling period for the greenhouse study. Measurements were taken in the top 2 cm of substrate.
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Fig. 3. Sediment pH values for the greenhouse study. Measurements were taken in the top 2 cm of substrate. Data points represent the means of all replicates averaged over north plot (NP) and south plot (SP) sediment for each sampling date.
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Fig. 4. Redox potential (Eh) and pH data from the control, compost, compost + low SO4, and compost + high SO4 treatments plotted on an EhpH diagram for a range of Pb minerals. This diagram does not take into account changes in stability based on variable sulfur concentrations.
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Fig. 5. Acid volatile sulfide (AVS) to simultaneously extracted metals (SEM) ratio from the tailings at the interface and bottom level (99 d) from amended and control treatments in the greenhouse study. Different letters above bars indicate significantly different values using the DuncanWaller means separation procedure (p < 0.05).
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Fig. 6. Stacked, normalized k3weighted LIIIextended X-ray adsorption fine structure (EXAFS) spectra (chi data) for lead in sediment samples taken after 99 d of incubation with various treatments, and mineral standards. Experimental spectra (solid lines) are overlaid with spectral fits (dashed lines) based on the fitting parameters reported in Table 5.
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Fig. 7. Stacked radial structure function (RSF) magnitudes derived by Fourier transformation of k3weighted, lead LIIIextended X-ray adsorption fine structure (EXAFS) spectra shown in Fig. 6. Radial distances are not corrected for phase shift, and therefore they do not reflect true interatomic distances.
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Fig. 8. Stacked, normalized LIIIX-ray absorption near edge structure (XANES) spectra for lead in sediment samples and standards. Sediment samples were collected at 99 d (solid line) or 207 d (dashed line) for each treatment. Data for standards are represented as solid lines for PbCO3 and PbSO4, and dashed lines for PbS and PbO.
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Copyright © 2003 by the American Society of Agronomy, Crop Science Society of America, and Soil Science Society of America.