Increased atmospheric deposition of mercury in reference lakes near major urban areas

Atmospheric deposition of Hg is the predominant pathway for Hg to reach sensitive ecosystems, but the importance of emissions on near-field deposition remains unclear. To better understand spatial variability in Hg deposition, mercury concentrations were analyzed in sediment cores from 12 lakes with undeveloped watersheds near to (<50 km) and remote from (>150 km) several major urban areas in the United States. Background and focusing corrected Hg fluxes and flux ratios (modern to background) in the near-urban lakes (68 ± 6.9 μg m−2 yr−1 and 9.8 ± 4.8, respectively) greatly exceed those in the remote lakes (14 ± 9.3 μg m−2 yr−1 and 3.5 ± 1.0) and the fluxes are strongly related to distance from the nearest major urban area (r2 = 0.87) and to population and Hg emissions within 50–100 km of the lakes. Comparison to monitored wet deposition suggests that dry deposition is a major contributor of Hg to lakes near major urban areas.

Graphical abstractFigure optionsDownload full-size imageDownload as PowerPoint slideHighlights► Hg deposition analyzed in cores from 6 near-urban and 6 remote reference lakes. ► Focus and background corrected Hg flux is ∼4.5 times greater near major cities. ► Strong relation (r2 = 0.87) between Hg deposition and distance from nearest city.