Journal
AQUATIC TOXICOLOGY
Volume 150, Issue -, Pages 36-44Publisher
ELSEVIER SCIENCE BV
DOI: 10.1016/j.aquatox.2014.02.012
Keywords
Nickel; Snail; Chronic toxicity; Growth; Uptake kinetics; Ion homeostasis
Categories
Funding
- NSERC [312017-2011]
- University of Saskatchewan
- NSF Graduate Research Fellowship
- NSF Post-Doctoral Fellowship
- SETAC/ICA Chris Lee Award for Metals Research
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The freshwater pulmonate snail, Lymnaea stagnalis, is the most sensitive aquatic organism tested to date for Ni. We undertook a series of experiments to investigate the underlying mechanism(s) for this observed hypersensitivity. Consistent with previous experiments, juvenile snail growth in a 21-day exposure was reduced by 48% relative to the control when exposed to 1.3 mu gl(-1) Ni (EC20 less than the lowest concentration tested). Ca2+ homeostasis was significantly disrupted by Ni exposure as demonstrated by reductions in net Ca2+ uptake, and reductions in Ca2+ concentrations in the hemolymph and soft tissues. We also observed reduced soft tissue [Mg2+]. Snails underwent a significant alkalosis with hemolymph pH increasing from 8.1 to 8.3 and hemolymph TCO2 increasing from 19 to 22 mM in control versus Ni-exposed snails, respectively. Unlike in previous studies with Co and Pb, snail feeding rates were found to be unaffected by Ni at the end of the exposure. Snails accumulated Ni in the soft tissue in a concentration-dependent manner, and Ni uptake experiments with Ni-63 revealed a biphasic uptake profile - a saturable high affinity component at low exposure concentrations (36-189 nM) and a linear component at the high exposure concentrations (189-1897 nM). The high affinity transport system had an apparent K-m of 89 nM Ni2+ and V-max of 2.4 nmol g(-1) h(-1). This equates to a log K of 7.1, significantly higher than log K's (2.6-5.2) for any other aquatic organisms evaluated to date, which will have implications for Biotic Ligand Model development. Finally, pharmacological inhibitors that block Ca2+ uptake pathways in snails did not inhibit Ni uptake, suggesting that the uptake of Ni does not occur via Ca2+ uptake pathways. As with Cu and Pb, the exact mechanism for the significant disruption in Ca2+ homeostasis and reduction in juvenile snail growth remains unknown. (C) 2014 Elsevier B.V. All rights reserved.
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