Observational analysis reveals natural emissions account for over 64% of total gaseous mercury, indicating shifts in emission sources.
The Canadian Air and Precipitation Monitoring Network (CAPMoN) measures total gaseous mercury (TGM) at three rural–remote sites. Long-term TGM measurements, ancillary measurements, and the positive matrix factorization (PMF) model were used to assess temporal changes in anthropogenic and natural surface emission (wildfires plus re-emitted Hg) contributions to TGM and examine the emission drivers of the observed TGM trends between 2005 and 2018. TGM showed decreasing trends at all sites; the magnitudes (ng m−3 yr−1) were −0.050 at Saturna for 2010–2015, −0.026 at Egbert for 2005–2018, and −0.014 at Kejimkujik for 2005–2016. The increasing contributions from natural surface Hg emissions at Saturna (1.8 % yr−1) and Kejimkujik (0.3 % yr−1) resulted from declining anthropogenic Hg emissions and increasing oceanic re-emissions. The mean relative contributions of natural surface emissions to annual TGM were 71 %, 77.5 %, and 64 % at Saturna, Egbert, and Kejimkujik. TGM at Saturna was mainly from the Hg pool (50 %), terrestrial re-emissions (26 %), and shipping (10 %); at Egbert, from the Hg pool (66 %), terrestrial re-emissions (24 %), and crustal/soil dust (5 %); and at Kejimkujik, from the Hg pool (81 %), regional Hg emissions (11 %), and oceanic re-emissions (8 %). Local combustion contributed a few percent of the annual TGM, while the oceanic re-emission contribution was 6 %–8 % for the two coastal sites. Wildfire impacts on annual TGM were 3.7 % for Saturna and 1.6 % for Egbert. The Hg pool contributions to TGM were greater in the cold season, whereas wildfire and surface re-emission contributions can be significant in the warm season.
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Cheng et al. (2025) studied this question.
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