Atmosphere‐surface exchange of mercury in a forest: Results of modeling and gradient approaches

Abstract

We have modified recently published dry deposition models to estimate deposition velocities (Vd) for Hg in both fine aerosol and vapor form to forest canopy surfaces. Aerosol and total vapor phase Hg concentrations in air previously measured at Walker Branch Watershed in Tennessee have been used with model results to estimate dry deposition to a deciduous forest. The concentration data confirm that airborne Hg is dominated by vapor forms at this site and exhibits concentrations moderately above continental background levels. The modeled Vd values reflect published data which suggest that dry deposition of Hg vapor is strongly controlled by surface transport processes, notably stomatal and mesophyll resistances, the latter dominating. Weekly mean Vd values ranged from 0.006 (winter) to 0.12 (summer) cm s−1. We have also measured concentration gradients of Hg vapor in air above this forest to estimate air‐surface exchange during short‐term experiments. While the model results indicate that the canopy is a sink for Hg vapor, the concentration profiles suggest that the forest soils are a source during some periods, the combined effect of which is net Hg fluxes in the upward direction. Application of a detailed canopy turbulence model yielded soil emission rates of the order of 50 ng Hg m−2 h−1, ∼10% of which is deposited in the canopy. Our modeled dry deposition estimates plus limited measurements of wet deposition in this area suggest that dry and wet deposition may be comparable in magnitude.