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Understanding small-scale features in DGT measurements in sediments.

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Understanding small-scale features in DGT measurements in sediments. / Sochaczewski, Łukasz; Davison, William; Zhang, Hao et al.
In: Environmental Chemistry, Vol. 6, No. 6, 2009, p. 477-485.

Research output: Contribution to Journal/MagazineJournal articlepeer-review

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Sochaczewski Ł, Davison W, Zhang H, Tych W. Understanding small-scale features in DGT measurements in sediments. Environmental Chemistry. 2009;6(6):477-485. doi: 10.1071/EN09077

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Sochaczewski, Łukasz ; Davison, William ; Zhang, Hao et al. / Understanding small-scale features in DGT measurements in sediments. In: Environmental Chemistry. 2009 ; Vol. 6, No. 6. pp. 477-485.

Bibtex

@article{14813f00323542328579ad59ff9e4174,
title = "Understanding small-scale features in DGT measurements in sediments.",
abstract = "Measurements in sediments made using DGT (diffusive gradients in thin-films) have shown small-scale (millimetre and sub-millimetre) maxima in solute concentration (e.g trace metals and sulfide). The sediment–DGT system was simulated using a dynamic model, which incorporated a spherical microniche close to the DGT surface. DGT maxima could arise when the microniche was (1) a local source with associated elevated concentration in the pore water, and (2) when, within the microniche, the Kd for the relevant solute partitioning with exchangeable solute associated with the solid phase was much higher than for the rest of the sediment. Use of realistic values of Kd and comparison with existing data suggested that the latter mechanism was unlikely to be responsible for observed DGT maxima. Locally elevated concentrations will be reasonably accurately reproduced by DGT. Peak height measured by DGT will be between 62 and 87% of the true maxima in concentration within the sediment when DGT is not present, while peak widths will be similar. This work provides, for the first time, a means for confidently interpreting the two dimensional images of DGT-measured concentrations in sediments.",
keywords = "microniche, sulfide, trace metals",
author = "{\L}ukasz Sochaczewski and William Davison and Hao Zhang and Wlodek Tych",
year = "2009",
doi = "10.1071/EN09077",
language = "English",
volume = "6",
pages = "477--485",
journal = "Environmental Chemistry",
issn = "1448-2517",
publisher = "CSIRO",
number = "6",

}

RIS

TY - JOUR

T1 - Understanding small-scale features in DGT measurements in sediments.

AU - Sochaczewski, Łukasz

AU - Davison, William

AU - Zhang, Hao

AU - Tych, Wlodek

PY - 2009

Y1 - 2009

N2 - Measurements in sediments made using DGT (diffusive gradients in thin-films) have shown small-scale (millimetre and sub-millimetre) maxima in solute concentration (e.g trace metals and sulfide). The sediment–DGT system was simulated using a dynamic model, which incorporated a spherical microniche close to the DGT surface. DGT maxima could arise when the microniche was (1) a local source with associated elevated concentration in the pore water, and (2) when, within the microniche, the Kd for the relevant solute partitioning with exchangeable solute associated with the solid phase was much higher than for the rest of the sediment. Use of realistic values of Kd and comparison with existing data suggested that the latter mechanism was unlikely to be responsible for observed DGT maxima. Locally elevated concentrations will be reasonably accurately reproduced by DGT. Peak height measured by DGT will be between 62 and 87% of the true maxima in concentration within the sediment when DGT is not present, while peak widths will be similar. This work provides, for the first time, a means for confidently interpreting the two dimensional images of DGT-measured concentrations in sediments.

AB - Measurements in sediments made using DGT (diffusive gradients in thin-films) have shown small-scale (millimetre and sub-millimetre) maxima in solute concentration (e.g trace metals and sulfide). The sediment–DGT system was simulated using a dynamic model, which incorporated a spherical microniche close to the DGT surface. DGT maxima could arise when the microniche was (1) a local source with associated elevated concentration in the pore water, and (2) when, within the microniche, the Kd for the relevant solute partitioning with exchangeable solute associated with the solid phase was much higher than for the rest of the sediment. Use of realistic values of Kd and comparison with existing data suggested that the latter mechanism was unlikely to be responsible for observed DGT maxima. Locally elevated concentrations will be reasonably accurately reproduced by DGT. Peak height measured by DGT will be between 62 and 87% of the true maxima in concentration within the sediment when DGT is not present, while peak widths will be similar. This work provides, for the first time, a means for confidently interpreting the two dimensional images of DGT-measured concentrations in sediments.

KW - microniche

KW - sulfide

KW - trace metals

U2 - 10.1071/EN09077

DO - 10.1071/EN09077

M3 - Journal article

VL - 6

SP - 477

EP - 485

JO - Environmental Chemistry

JF - Environmental Chemistry

SN - 1448-2517

IS - 6

ER -