The Legacy of Mercury Contamination from Colonial Nonferrous Mining in the Southern Hemisphere

TL;DR

This study examines mercury pollution from a historical copper mine in Tasmania, showing how smelting methods significantly impacted mercury emissions and environmental contamination.

Contribution

The study provides the first record of mercury concentrations and accumulation rates from lakes near the Mount Lyell mine, highlighting the impact of smelting methods.

Findings

Mercury concentrations and accumulation rates increased with smelting and peaked with the introduction of flotation processing.

Mercury isotopic signatures confirmed the anthropogenic origin of mercury emissions from the mine.

The estimated total mercury loadings from the mine ranged from 23 to 43 tons.

Abstract

The Mount Lyell copper (Cu) mine in Tasmania, Australia,
underwent
historical operational changes that influenced mercury (Hg) emissions
from ore processing and smelting. This study presents the first record
of Hg concentrations (HgC) and accumulation rates (HgAR) using sediment cores from four lakes around Mount Lyell.
HgC and HgAR increased from the 1890s (onset
of smelting), peaked from the 1920s (introduction of the flotation
processing method), and declined after 1969 (smelter closure). Mercury
isotopic signatures confirmed its anthropogenic source. Modeling of
Hg deposition vs distance over the period 1922–1969 showed
that it followed a power-law function. The Mount Lyell emissions may
have affected an area up to ∼270,000 km2, beyond
which deposition was indistinguishable from the natural background.
Estimated total Hg loadings ranged from 23 to 43 t, compared to an
estimated ∼150 t Hg contained in the ore floated. Isotopic
data showed Δ199Hg trending toward zero near the
smelter, indicating that the smelter was the main source of Hg. Our
findings highlight that pyrometallurgical smelting methods contributed
more significantly to Hg emissions than production volume. Studying
legacy mines in the Southern Hemisphere, responsible for 29.1% of
global Cu production during the preregulatory era (1880–1950),
is critical to understanding historical Hg dispersion in this understudied
region.

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