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Waterborne carbon increases threat of environmental mercury
Date:12/10/2007

tial to geochemical variables," Moreau says. "We would like to take a bacterium that we know methylates mercury very efficiently and let it tell us what it can methylate and what it can't, under given conditions."

Moreau and colleagues at the U.S. Geological Survey, UW-Madison, the University of Colorado and Chapman University chose to look at the role of dissolved organic carbon (DOC), a richly colored brew created as plants and other organic materials decay into a soup of proteins, acids and other compounds. DOC can tint wetlands and streams shades of yellow to dark brown.

DOC has noticeable effects on bacterial mercury processing. "They seem to methylate mercury better with DOC present," says Moreau.

In the current studies, the scientists looked at the effects of DOC samples collected from two different organic-rich environments, a section of the Suwannee River and Florida's Everglades.

"We found that different DOCs have different positive effects on methylation - they both seem to promote mercury methylation, but to different degrees," Moreau explains.

Because DOC is virtually ubiquitous in aqueous environments, its effect on mercury processing may be an important factor in determining mercury bioavailability.

Moreau and his colleagues are now working to understand how DOC promotes methylation. One possibility is that DOC acts indirectly by increasing bacterial growth, while another is that DOC may directly interact with the mercury itself to boost its ability to enter bacteria.

Although mercury already in the environment is there to stay, Moreau says an understanding of what regulates mercury toxicity is critical for developing ecosystem-level management strategies.

"Strategies to deal with methylmercury production [should] lead to hopefully more efficient ways to reduce human consumption of methylmercury and lead to less potential human health problems," he says.


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Contact: John Moreau
moreau@geology.wisc.edu
University of Wisconsin-Madison
Source:Eurekalert

Page: 1 2

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Contains L-glutamine
Clone/PAD: ZMD.358. Immunogen: Synthetic peptide derived from the C-terminal region of human mouse and rat LRP5. Specificity: Reacts with human and mouse LRP5 proteins. Reactivity: Mouse Human (po
Replacement Parts for Electrophoresis Apparatus
Sprague-Dawley rats, 7-8 weeks old, mixed gender; tissue is collected fresh, frozen on dry ice within minutes of sacrifice and stored at -20C; individual tissue weight approx. 0.05 gram.
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