Journal
EARTH AND PLANETARY SCIENCE LETTERS
Volume 472, Issue -, Pages 309-322Publisher
ELSEVIER
DOI: 10.1016/j.epsl.2017.05.025
Keywords
volcanic plume; volcanic emissions; volcanic eruption; air quality; environment; Iceland
Categories
Funding
- NERC [NE/M021130/1]
- European Research Council under the European Union's Seventh Framework Programme (FP)/ERC [279802]
- European Community's Seventh Framework Programme [308377]
- NERC
- University of Birmingham through the Elite Scholar scheme
- NERC [come30001, NE/M021130/1] Funding Source: UKRI
- Natural Environment Research Council [come30001, NE/M021130/1] Funding Source: researchfish
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The 2014-2015 Holuhraun eruption in Iceland, emitted similar to 11 Tg of SO2 into the troposphere over 6 months, and caused one of the most intense and widespread volcanogenic air pollution events in centuries. This study provides a number of source terms for characterisation of plumes in large fissure eruptions, in Iceland and elsewhere. We characterised the chemistry of aerosol particle matter (PM) and gas in the Holuhraun plume, and its evolution as the plume dispersed, both via measurements and modelling. The plume was sampled at the eruptive vent, and in two populated areas in Iceland. The plume caused repeated air pollution events, exceeding hourly air quality standards (350 mu g/m(3)) for SO2 on 88 occasions in Reykjahlio town (100 km distance), and 34 occasions in Reykjavik capital area (250 km distance). Average daily concentration of volcanogenic PM sulphate exceeded 5 mu g/m(3) on 30 days in Reykjavik capital area, which is the maximum concentration measured during non-eruptive background interval. There are currently no established air quality standards for sulphate. Combining the results from direct sampling and dispersion modelling, we identified two types of plume impacting the downwind populated areas. The first type was characterised by high concentrations of both SO2 and S-bearing PM, with a high S-gas/S-PM mass ratio (SO2(g)/SO4(pm)2- > 10). The second type had a low S-gas/S-PM ratio (<10). We suggest that this second type was a mature plume where sulphur had undergone significant gas to-aerosol conversion in the atmosphere. Both types of plume were rich in fine aerosol (predominantly PM1 and PM2.5), sulphate (on average similar to 90% of the PM mass) and various trace species, including heavy metals. The fine size of the volcanic PM mass (75-80% in PM2.5), and the high environmental lability of its chemical components have potential adverse implications for environmental and health impacts. However, only the dispersion of volcanic SO2 was forecast in public warnings and operationally monitored during the eruption. We make a recommendation that sulphur gas-to-aerosol conversion processes, and a sufficiently large model domain to contain the transport of a tropospheric plume on the timescale of days be utilized for public health and environmental impact forecasting in future eruptions in Iceland and elsewhere in the world. (C) 2017 The Author(s). Published by Elsevier B.V.
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