TY - JOUR
T1 - Anaerobic guilds responsible for mercury methylation in boreal wetlands of varied trophic status serving as either a methylmercury source or sink
AU - Schaefer, Jeffra K.
AU - Kronberg, Rose Marie
AU - Björn, Erik
AU - Skyllberg, Ulf
N1 - Funding Information:
The authors thank C. Cobb‐Adams for extraction of nucleic acids, and F. Morel for use of laboratory space and equipment. The authors also thank S. Roth and T. Barkay for assistance with Illumina sequencing and many helpful discussions regarding this project. This research was funded by grants from the Swedish Research Council for Environment and Spatial Planning (FORMAS, no. 29‐2009‐1207) and CMF‐Umeå (No. 0822333) to U. S., Kempestiftelserna (SMK‐1243, SMK‐2745) to E. B. and U. S, and the U.S. Dept. of Energy Office of Science, Biological and Environmental Research, Subsurface Biogeochemical Research Program (No. DE‐SC0006849) and Rutgers University Research Council grant to J. S.
Publisher Copyright:
© 2020 Society for Applied Microbiology and John Wiley & Sons Ltd.
PY - 2020/9/1
Y1 - 2020/9/1
N2 - Wetlands are common sites of active Hg methylation by anaerobic microbes; however, the amount of methylmercury produced varies greatly, as Hg methylation is dependent upon both the availability of Hg and the composition and activity of the microbial community involved. In this study, we identified the major microbial guilds responsible for Hg methylation along a trophic gradient composed of two sites and three different types of wetlands: a bog–fen peatland gradient and a black alder swamp, serving as net sources and a sink for methylmercury respectively. Iron-reducing bacteria in the Geobacteraceae were important Hg methylators across all wetlands and seasons examined, as evidenced by abundant 16S rRNA and hgcA transcripts clustering with this family. Molybdate inhibited Hg methylation more efficiently in the peatlands than in the swamp, suggesting an increasing role of sulfate-reducing bacteria and/or related syntrophs in the methylation of Hg with decreasing trophic status. Sulfate addition failed to increase Hg methylation rates in the peatlands, suggesting that SRBs/syntrophs were instead likely metabolizing alternative substrates such as syntrophic fermentation of organic compounds with methanogens. These results highlight the interconnectivity of anaerobic metabolism and importance of community dynamics on the methylation of Hg in wetlands with different trophic status.
AB - Wetlands are common sites of active Hg methylation by anaerobic microbes; however, the amount of methylmercury produced varies greatly, as Hg methylation is dependent upon both the availability of Hg and the composition and activity of the microbial community involved. In this study, we identified the major microbial guilds responsible for Hg methylation along a trophic gradient composed of two sites and three different types of wetlands: a bog–fen peatland gradient and a black alder swamp, serving as net sources and a sink for methylmercury respectively. Iron-reducing bacteria in the Geobacteraceae were important Hg methylators across all wetlands and seasons examined, as evidenced by abundant 16S rRNA and hgcA transcripts clustering with this family. Molybdate inhibited Hg methylation more efficiently in the peatlands than in the swamp, suggesting an increasing role of sulfate-reducing bacteria and/or related syntrophs in the methylation of Hg with decreasing trophic status. Sulfate addition failed to increase Hg methylation rates in the peatlands, suggesting that SRBs/syntrophs were instead likely metabolizing alternative substrates such as syntrophic fermentation of organic compounds with methanogens. These results highlight the interconnectivity of anaerobic metabolism and importance of community dynamics on the methylation of Hg in wetlands with different trophic status.
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U2 - 10.1111/1462-2920.15134
DO - 10.1111/1462-2920.15134
M3 - Article
C2 - 32558127
AN - SCOPUS:85088302914
SN - 1462-2912
VL - 22
SP - 3685
EP - 3699
JO - Environmental Microbiology
JF - Environmental Microbiology
IS - 9
ER -