Abstract
AbstractIncreasing mercury isotope ratios from pre‐industrial (1510–1850) to present‐day (1990–2014) in lake sediment cores have been suggested to be a global phenomenon. To assess factors leading to spatiotemporal changes, we compiled mercury concentration (THg) and mercury isotope ratios in 22 lake sediment cores located at various regions of the world. We find that the positive δ202Hg shifts together with THg increases from pre‐industrial to present‐day are a widespread phenomenon. This is caused by increased contribution of mercury from local to regional anthropogenic mercury emission sources, which lead to higher sediment δ202Hg (−1.07 ± 0.69‰, 1 SD) than pre‐industrial sediments (−1.55 ± 0.96‰, 1 SD). The positive Δ199Hg shifts were observed in 15 lake sediment cores, which have low pre‐industrial Δ199Hg (−0.20 ± 0.32‰) compared to the sediment cores with near‐zero to positive pre‐industrial Δ199Hg (0.08 ± 0.07‰). The magnitudes of δ202Hg (r2 = 0.09) and Δ199Hg (r2 = 0.20, both p > 0.05) changes from pre‐industrial to present‐day did not correlate with the magnitude of THg changes. Instead, the magnitudes of δ202Hg and Δ199Hg changes decreased with increasing pre‐industrial δ202Hg and Δ199Hg values, suggesting that the baseline mercury isotope ratios play a more important role in determining the magnitude of mercury isotope changes compared to the degree of THg input. We suggest that the spatiotemporal assessments of δ202Hg in lake sediment cores can be used as an important proxy for monitoring changes in anthropogenic mercury sources for the Minamata Convention on Mercury.
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