Sediment aggregation and water quality in wildfire-affected river basins
W. H. Blake A D , P. J. Wallbrink B and I. G. Droppo CA School of Geography, University of Plymouth, Plymouth PL4 8AA, UK.
B CSIRO Land and Water, Canberra, ACT 2601, Australia.
C National Water Resources Institute, Environment Canada, Burlington, ON L7R 4A6, Canada.
D Corresponding author. Email: william.blake@plymouth.ac.uk
Marine and Freshwater Research 60(7) 653-659 https://doi.org/10.1071/MF08068
Submitted: 1 March 2008 Accepted: 22 February 2009 Published: 28 July 2009
Abstract
Off-site transfer of nutrient-rich burnt soil has implications for downstream water quality. Coarsening of effective particle size (EPS) distributions in burnt material via aggregation of fines into composite particles modifies post-fire sediment and nutrient transport dynamics. Experiments were undertaken to establish temperature controls on wildfire-enhanced soil aggregation. Burnt and unburnt soil from a temperate eucalypt forest were analysed for EPS and settling velocity using a LISST-ST (Laser In Situ Scatter and Transmissometry with Settling Tube) particle size analyser. Next, samples were burnt (250–550°C) before further analysis with the LISST-ST. Settling velocities of naturally burnt soil aggregates were greater than unburnt aggregates of the same EPS. Experimental burning indicated that dense water-stable aggregates form at relatively low temperatures (250°C) probably due to distillation and carbonisation, through pyrolysis, of organic volatiles in surface litter. Under these conditions, the EPS distribution of burnt surface soil coarsens with up to 50% of the <63-μm fraction becoming aggregated. A positive relationship between ‘plant-available’ phosphorus and burn temperature was observed. Given that a large proportion of soil particulate phosphorus is associated with the <63-μm fraction, fire-related aggregation processes have potentially important implications for post-fire fine sediment and nutrient transport and storage dynamics.
Additional keywords: phosphorus, soil aggregate.
Acknowledgements
This work has been funded by two Royal Society overseas study visit awards to W.B. (to NWRI in Canada and CSIRO in Australia). CSIRO Land and Water are acknowledged for provision of laboratory space. The School of Geography, University of Plymouth is acknowledged for a research sabbatical to W.B. Kerrie Tomkins and the late Geoff Humphreys kindly assisted with the fieldwork. Kevin Solman undertook the geochemical analyses. We are grateful for constructive reviews and comments from Andrew Boulton, Brian Kronvang, Mike Stone and an anonymous reviewer.
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