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Cited by 472

The DOI matches its Crossref record; 25 of the 25 references it cites were found in a registry or an index.

Whole-ecosystem study shows rapid fish-mercury response to changes in mercury deposition

Open access
Harris, Reed C., Rudd, John W. M., Amyot, Marc, Babiarz, Christopher L., Beaty, Ken G., Blanchfield, Paul J., Bodaly, R. A., Branfireun, Brian A., Gilmour, Cynthia C., Graydon, Jennifer A., Heyes, Andrew, Hintelmann, Holger, Hurley, James P., Kelly, Carol A., Krabbenhoft, David P., Lindberg, Steve E., Mason, Robert P., Paterson, Michael J., Podemski, Cheryl L., Robinson, Art, Sandilands, Ken A., Southworth, George R., St. Louis, Vincent L., Tate, Michael T.·2007·Proceedings of the National Academy of Sciences

Abstract

Methylmercury contamination of fisheries from centuries of industrial atmospheric emissions negatively impacts humans and wildlife worldwide. The response of fish methylmercury concentrations to changes in mercury deposition has been difficult to establish because sediments/soils contain large pools of historical contamination, and many factors in addition to deposition affect fish mercury. To test directly the response of fish contamination to changing mercury deposition, we conducted a whole-ecosystem experiment, increasing the mercury load to a lake and its watershed by the addition of enriched stable mercury isotopes. The isotopes allowed us to distinguish between experimentally applied mercury and mercury already present in the ecosystem and to examine bioaccumulation of mercury deposited to different parts of the watershed. Fish methylmercury concentrations responded rapidly to changes in mercury deposition over the first 3 years of study. Essentially all of the increase in fish methylmercury concentrations came from mercury deposited directly to the lake surface. In contrast, <1% of the mercury isotope deposited to the watershed was exported to the lake. Steady state was not reached within 3 years. Lake mercury isotope concentrations were still rising in lake biota, and watershed mercury isotope exports to the lake were increasing slowly. Therefore, we predict that mercury emissions reductions will yield rapid (years) reductions in fish methylmercury concentrations and will yield concomitant reductions in risk. However, a full response will be delayed by the gradual export of mercury stored in watersheds. The rate of response will vary among lakes depending on the relative surface areas of water and watershed.

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Metadata

Authors
Harris, R. C., Rudd, J. W. M., Amyot, M., Babiarz, C. L., Beaty, K. G., Blanchfield, P. J., Bodaly, R. A., Branfireun, B. A., Gilmour, C. C., Graydon, J. A., Heyes, A., Hintelmann, H., Hurley, J. P., Kelly, C. A., Krabbenhoft, D. P., Lindberg, S. E., Mason, R. P., Paterson, M. J., Podemski, C. L., Robinson, A., Sandilands, K. A., Southworth, G. R., St. Louis, V. L., & Tate, M. T.
Venue
Proceedings of the National Academy of Sciences
Published
2007-10-16
Volume
104
Issue
42
Pages
16586-16591
ISSN
  • 0027-8424 (ISSN-L)
  • 1091-6490
OpenAlex
W2095313883
Cited by
472
References
25
FWCI
18.00
Type
journal article
Language
en
Open access
bronze

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CoChat. (2026). Citation check: Whole-ecosystem study shows rapid fish-mercury response to changes in mercury deposition. https://app.cochat.ai/papers/10.1073/pnas.0704186104
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Harris, R. C., Rudd, J. W. M., Amyot, M., Babiarz, C. L., Beaty, K. G., Blanchfield, P. J., Bodaly, R. A., Branfireun, B. A., Gilmour, C. C., Graydon, J. A., Heyes, A., Hintelmann, H., Hurley, J. P., Kelly, C. A., Krabbenhoft, D. P., Lindberg, S. E., Mason, R. P., Paterson, M. J., Podemski, C. L., . . . Tate, M. T. (2007). Whole-ecosystem study shows rapid fish-mercury response to changes in mercury deposition. Proceedings of the National Academy of Sciences. https://doi.org/10.1073/pnas.0704186104

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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.