4.7 Article

Quantity, composition and water contamination potential of ash produced under different wildfire seventies

Journal

ENVIRONMENTAL RESEARCH
Volume 142, Issue -, Pages 297-308

Publisher

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.envres.2015.06.041

Keywords

Forest fire; Bushfire; Ash chemistry; Water quality; Soil erosion

Funding

  1. Water NSW
  2. Leverhulme Trust [RPG-2014-95]
  3. PROMETEO project (SENESCYT-Ecuador)

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Wildfires frequently threaten water quality through the transfer of eroded ash and soil into rivers and reservoirs. The ability to anticipate risks for water resources from wildfires is fundamental for implementing effective fire preparedness plans and post-fire mitigation measures. Here we present a new approach that allows quantifying the amount and characteristics of ash generated under different wildfire severities and its respective water contamination potential. This approach is applied to a wildfire in an Australian dry sclerophyll eucalypt forest, but can be adapted for use in other environments. The Balmoral fire of October 2013 affected 12,694 ha of Sydney's forested water supply catchment. It produced substantial ash loads that increased with fire severity, with 6, 16 and 34 Mg ha(-1) found in areas affected by low, high and extreme fire severity, respectively. Ash bulk density was also positively related to fire severity. The increase with fire severity in the total load and bulk density of the ash generated is mainly attributed to a combination of associated increases in (i) total amount of fuel affected by fire and (ii) contribution of charred mineral soil to the ash layer. Total concentrations of pollutants and nutrients in ash were mostly unrelated to fire severity and relatively low compared to values reported for wildfire ash in other environments (e.g. 4.0-7.3 mg As kg(-1); 2.3-4.1 B mg kg(-1); 136-154 P mg kg). Solubility of the elements analysed was also low, less than 10% of the total concentration for all elements except for B (6-14%) and Na (30-50%). This could be related to a partial loss of soluble components by leaching and/or wind erosion before the ash sampling (10 weeks after the fire and before major ash mobilisation by water erosion). Even with their relatively low concentrations of potential pollutants, the substantial total ash loads found here represent a water contamination risk if transported into the hydrological network during severe erosion events. For example, up to 4 Mg of ash-derived P could be delivered into a single water supply reservoir. (C) 2015 Elsevier Inc. All rights reserved.

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