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Natural dissolved organic matter plays dual role in cycling of mercury

Date:
January 13, 2011
Source:
DOE/Oak Ridge National Laboratory
Summary:
Nature has a bit of a Jekyll and Hyde relationship with mercury, but researchers have made a discovery that ultimately could help explain the split personality.

Findings published in Proceedings of the National Academy of Sciences by Oak Ridge National Laboratory's Liyuan Liang and Baohua Gu help explain previously reported seemingly contradictory findings.
Credit: ORNL photo by Jason Richards

Nature has a bit of a Jekyll and Hyde relationship with mercury, but researchers at the Department of Energy's Oak Ridge National Laboratory have made a discovery that ultimately could help explain the split personality.

While scientists have known that microbes in aquatic environments make methylmercury, a more toxic form of mercury that accumulates in fish, they also know that nature and other types of bacteria can transform methylmercury to less toxic forms. What they haven't completely understood are the mechanisms that cause these transformations in anoxic environments -- lacking in oxygen -- in nature.

"Until now, reactions between elemental mercury and dissolved organic matter have rarely been studied in anoxic environments," said Baohua Gu of the the lab's Environmental Sciences Division.

In a paper published in the Proceedings of the National Academy of Sciences, a team led by Gu reports that compounds from the decay of organic matter in aquatic settings affect mercury cycling. Low concentrations of these compounds can chemically reduce mercury, but as those concentrations increase, that reaction is greatly inhibited. They performed their experiments by simulating conditions found in nature.

"This study demonstrates that in anoxic sediments and water, organic matter is not only capable of reducing mercury, but also binding to mercury," said co-author Liyuan Liang. "This binding could make mercury less available to microorganisms for making methylmercury."

The authors also noted that their paper offers a mechanism that helps explain the seemingly contradictory reports on the interaction of organic matter and mercury in nature.

Gu and Liang hope this newly gained knowledge will play a role in helping to understand how mercury cycles in aquatic and sediment environments and help in informed decision-making for mercury-impacted sites around the nation.

"Our long-term goal is to understand the mechanisms controlling the production of methylmercury in the environment, " Liang said. "This understanding could lead to ways to reduce levels of mercury in fish as this is a global problem of enormous significance."

Mercury is distributed around the globe mainly through the burning of coal, industrial uses and through natural processes such as volcano eruptions. Various forms of mercury are widely found in sediments and water.

This research benefits from ORNL's expertise in field-to-laboratory geochemistry and microbiology, computational modeling and simulation, world-class neutron sources and high-performance computing.


Story Source:

The above story is based on materials provided by DOE/Oak Ridge National Laboratory. Note: Materials may be edited for content and length.


Journal Reference:

  1. B. Gu, Y. Bian, C. L. Miller, W. Dong, X. Jiang, L. Liang. Mercury reduction and complexation by natural organic matter in anoxic environments. Proceedings of the National Academy of Sciences, 2011; DOI: 10.1073/pnas.1008747108

Cite This Page:

DOE/Oak Ridge National Laboratory. "Natural dissolved organic matter plays dual role in cycling of mercury." ScienceDaily. ScienceDaily, 13 January 2011. <www.sciencedaily.com/releases/2011/01/110112160958.htm>.
DOE/Oak Ridge National Laboratory. (2011, January 13). Natural dissolved organic matter plays dual role in cycling of mercury. ScienceDaily. Retrieved September 20, 2014 from www.sciencedaily.com/releases/2011/01/110112160958.htm
DOE/Oak Ridge National Laboratory. "Natural dissolved organic matter plays dual role in cycling of mercury." ScienceDaily. www.sciencedaily.com/releases/2011/01/110112160958.htm (accessed September 20, 2014).

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