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Soils are the largest terrestrial pool of mercury (Hg), a neurotoxic pollutant. Pathways of Hg accumulation and loss in forest soils include throughfall, litterfall, soil gas fluxes, and leaching in soil solution, all of which will likely be altered under changing climate. We took advantage of three ongoing climate-change manipulation experiments at the Hubbard Brook Experimental Forest, New Hampshire, USA: a combined growing-season warming and winter freeze-thaw cycle experiment, a throughfall exclusion to mimic drought, and a simulated ice storm experiment to examine the response of the forest Hg cycle to climatic disturbances. Across these three experiments, we compared Hg inputs in throughfall and leaf litterfall and Hg outputs in soil gas fluxes. Soil solution was measured only in the simulated ice storm experiment. We found that northern forest soils retained consistently less Hg by 16–60% in the three climate manipulations compared to the undisturbed controls (~ 7.4 µg Hg m−2 year−1), although soils across all three experiments still served as a net sink for Hg. Growing-season soil warming and combined soil warming and winter freeze-thaw cycles had little effect on litterfall and throughfall flux, but they increased soil Hg0 evasion by 31 and 35%, respectively, relative to the control plots. The drought plots had 5% lower litterfall Hg flux, 50% lower throughfall Hg flux, and 21% lower soil Hg0 evasion than the control plots. The simulated ice storm had 23% higher litterfall Hg flux, 1% higher throughfall Hg flux, 37% higher soil Hg0 evasion, and 151% higher soil Hg leaching than the control plots. These observations suggest that climate changes such as warmer soils in the growing season or more intense ice storms in winter are likely to exacerbate Hg pollution by releasing Hg sequestered in forest soils via evasion and leaching. [ABSTRACT FROM AUTHOR]

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There is concern that changes in atmospheric deposition, climate, or land use have altered the biogeochemistry of forests causing soil base-cation depletion, particularly Ca. The Bear Brook Watershed in Maine (BBWM) is a paired watershed experiment with one watershed subjected to elevated N and S deposition through bimonthly additions of (NH[sub 4])[sub 2]SO[sub 4]. Quantitative soil excavations in 1998 measured soil pools of exchangeable base cations 9 yr after treatments began. Stream sampling at the weirs on a weekly and event basis, and weekly precipitation sampling, were used for input-output estimates. The treated watershed had lower concentrations of exchangeable Ca and Mg in all horizons, with evidence for the greater depletion in the O horizon compared to underlying mineral soils, and in softwoods compared to hardwoods. This difference between watersheds is interpreted to be treatment-induced base-cation depletion, which was reinforced by model simulations. The difference between watersheds was 66 and 27 kg ha[sup -1] of exchangeable Ca and Mg, respectively, after accounting for soil mass differences between watersheds. This was comparable with the total cumulative excess stream Ca and Mg export in West Bear after 9 yr of treatment of 55 and 11 kg ha[sup -1], respectively. Model simulations of watershed response to treatments predicted excess soil exchangeable Ca and Mg losses in the treated watershed of 47 and 9 kg ha[sup -1], respectively. These results indicate that the response to a step-increase in N and S deposition during the first decade of treatments in this experimental forested watershed was to invoke cationexchange buffering, resulting in a net decline in soil exchangeable base cations. [ABSTRACT FROM AUTHOR]

Evaluates the effects of nitrogen (N) enrichment, wildfire and harvesting on forest-soil carbon (C) and N. Reduction of forest-floor C/N ratios; Comparison of forest-floor C and N pools in the treated watershed and reference watershed; Comparison of C and N concentrations and pools in the burned watershed with hardwood and the reference with softwoods.