Importance of equilibration time in the partitioning and toxicity of zinc in spiked sediment bioassays

被引:28
作者
Lee, JS
Lee, BG
Luoma, SN
Yoo, H
机构
[1] US Geol Survey, Menlo Pk, CA 94025 USA
[2] NeoEnBiz Co, Seoul, South Korea
[3] Chonnam Natl Univ, Dept Oceanog, Kwangju 500757, South Korea
关键词
zinc; toxicity; equilibration time; sediment aging; acid volatile sulfides;
D O I
10.1897/03-176
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
The influences of spiked Zn concentrations (1-40 mumol/g) and equilibration time (similar to95 d) on the partitioning of Zn between pore water (PW) and sediment were evaluated with estuarine sediments containing two levels (5 and 15 mumol/g) of acid volatile sulfides (AVS). Their influence on Zn bioavailability was also evaluated by a parallel, 10-d amphipod (Leptocheirus plumulosus) mortality test at 5, 20, and 85 d of equilibration. During the equilibration, AVS increased (up to twofold) with spiked Zn concentration ([Zn]), whereas Zn-simultaneously extracted metals ([SEM]; Zn with AVS) remained relatively constant. Concentrations of Zn in PW decreased most rapidly during the initial 30 d and by 11- to 23-fold during the whole 95-d equilibration period. The apparent partitioning coefficient (K(pw,) ratio of [Zn] in SEM to PW) increased by 10- to 20-fold with time and decreased with spiked [Zn] in sediments. The decrease of PW [Zn] could be explained by a combination of changes in AVS and redistribution of Zn into more insoluble phases as the sediment aged. Amphipod mortality decreased significantly with the equilibration time, consistent with decrease in dissolved [Zn]. The median lethal concentration (LC50) value (33 muM) in the second bioassay, conducted after 20 d of equilibration, was twofold the LC50 in the initial bioassay at 5 d of equilibration, probably because of the change of dissolved Zn speciation. Sediment bioassay protocols employing a short equilibration time and high spiked metal concentrations could accentuate partitioning of metals to the dissolved phase and shift the pathway for metal exposure toward the dissolved phase.
引用
收藏
页码:65 / 71
页数:7
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