ABSTRACTMercury (Hg) in tree wood has been overlooked, in part because concentrations are so low as to be below detection limits of some analytical methods, but it is potentially important to forest ecosystem processes and budgets. We tested methods for the preparation and determination of Hg in tree wood by analysing samples of four tree species at the Hubbard Brook Experimental Forest, New Hampshire, USA, using thermal decomposition, catalytic conversion, amalgamation and atomic absorption spectrophotometry (USEPA Method 7473). Samples that were freeze-dried or oven-dried at 65°C were suitable for determination of Hg, whereas oven-drying at 103°C resulted in Hg losses, and air-drying resulted in Hg gains, presumably due to sorption from indoor air. Mean (±SE) concentrations of Hg tree bole wood were 1.75 ± 0.14 ng g−1 for American beech, 1.48 ± 0.23 ng g−1 for sugar maple, 3.96 ± 0.19 ng g−1 for red spruce and 4.59 ± 0.06 ng g−1 for balsam fir. Based on these concentrations and estimates of wood biomass by species based on stand inventory, we estimated the Hg content of wood in the reference watershed at Hubbard Brook to be 0.32 g ha−1, twice the size of the foliar Hg pool (0.15 g ha−1). Mercury in wood deserves more attention and is feasible to measure using appropriate techniques.
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