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Quantifying soil accumulation of atmospheric mercury using fallout radionuclide chronometry
Joshua D Landis1, Daniel Obrist2,3, Jun Zhou4
1Department of Earth Sciences, Dartmouth College, Hanover, NH, 03755, USA. joshua.d.landis@dartmouth.edu.
Nature Communications
|June 26, 2024
Summary
Soils retain most mercury (Hg) despite atmospheric deposition. Significant re-emission of mercury as gaseous elemental mercury (GEM) is limited, challenging global models and highlighting FRN chronometry for Hg accumulation studies.
Area of Science:
- Environmental Science
- Geochemistry
- Atmospheric Chemistry
Background:
- Soils are major global reservoirs for mercury (Hg), a neurotoxic pollutant.
- Anthropogenic emissions lead to Hg accumulation in terrestrial ecosystems.
- Uncertainty exists regarding the fate of soil Hg, especially re-emission as gaseous elemental mercury (GEM).
Purpose of the Study:
- To directly measure Hg accumulation rates in diverse soil types.
- To assess the quantitative efficiency of Hg retention in soils.
- To evaluate the potential for GEM re-emission from soils and challenge existing global models.
Main Methods:
- Utilized fallout radionuclide (FRN) chronometry to determine Hg accumulation rates.
- Employed a mass balance approach comparing accumulation rates with atmospheric Hg fluxes.
- Analyzed soils from Arctic, boreal, temperate, and tropical regions.
Main Results:
- Soils across various biomes demonstrate high efficiency in retaining anthropogenic Hg.
- Significant GEM re-emission potential is primarily restricted to a subset of coniferous soils.
- Findings contradict global models that assume substantial legacy Hg re-emission from soils.
Conclusions:
- Most soils are effective sinks for atmospheric mercury, limiting widespread GEM re-emission.
- FRN chronometry is a powerful technique for reconstructing terrestrial Hg accumulation at broad scales.
- Further research is needed to understand Hg mobilization susceptibility across different soil environments.

