Effect of season and landscape position on the aluminium geochemistry of tropical acid sulfate soil leachate
W. S. Hicks A D , G. M. Bowman B and R. W. Fitzpatrick CA CSIRO Land & Water, GPO Box 1666, Canberra, ACT 2601, Australia.
B NSW Department of Environment and Climate Change, PO Box 622, Queanbeyan, NSW 2620, Australia.
C CSIRO Land and Water, PB No. 2, Glen Osmond, SA 5064, Australia.
D Corresponding author. Email: warren.hicks@csiro.au
Australian Journal of Soil Research 47(2) 137-153 https://doi.org/10.1071/SR06106
Submitted: 11 August 2006 Accepted: 17 October 2008 Published: 31 March 2009
Abstract
Acid sulfate soils (ASS) occupy an estimated 5.8 × 106 ha of coastal Australia. In tropical Australia, the processes operating in these soils, and their environmental hazards, are poorly understood. Drainage of a tropical estuarine wetland containing extensive ASS deposits left the area in a highly degraded condition. Surface and soil water pH values from the site were consistently <5 and commonly <3.5. Aluminium activity was several orders of magnitude greater than the level set for the protection of aquatic ecosystems, with a seasonal variation of 3 orders of magnitude. Aluminium behaved conservatively at the discharge point to receiving waters. In drainage lines and soil solution, aluminium activity was limited by elevated sulfate activity. Aluminium was commonly supersaturated with respect to alunite and behaved as though an aluminium species with the stoichiometry Al:OH:SO4 regulated its activity, which was 2–5 orders of magnitude lower than if gibbsite or amorphous aluminium hydroxide solubility was the control. While jurbanite (AlOHSO4.5H2O) is no longer considered a potential mineral in ASS, these data again raise the question of a satisfactory explanation of aluminium activity. Sulfate activity was influenced by seasonal factors. Wet season conditions were reducing and favoured the dissolution of acid iron oxidation products. The dry season oxidising and drying conditions favoured their precipitation, resulting in seasonal cycling. Based on our findings we developed a landscape geochemical process model for the site.
Acknowledgements
The authors thank staff of the Division’s Analytical Chemistry Unit, whose high quality analyses were vital to the thermodynamic calculations. We are also grateful to local landholders Norm and Edna Whitney, who carried out the sampling program over several years, often in the presence of torrential rain, stifling heat, hordes of biting insects and crocodiles. The authors would also like to thank the referees of an earlier version of this paper who provided detailed and helpful comments.
Adams F, Rawajfih Z
(1977) Basaluminite and alunite: a possible cause of sulfate retention by acid soils. Soil Science Society of America Journal 41, 686–692.
|
CAS |
(accessed 8 March 2006).
Nordstrom DK
(1982) The effect of sulfate on aluminium concentrations in natural waters: some stability relations in the system Al2O3-SO3-H2O at 298 K. Geochimica et Cosmochimica Acta 46, 681–692.
| Crossref | GoogleScholarGoogle Scholar |
CAS |
Nordstrom DK,
Plummer LN,
Langmuir D,
Busenberg E,
May HM,
Jones BF, Parkhurst DL
(1990) Revised chemical-equilibrium data for major water-mineral reactions and their limitations. ACS Symposium Series. American Chemical Society 416, 398–413.
|
CAS |
Prietzel J, Hirsch C
(1998) Extractability and dissolution kinetics of pure and soil added synthesized aluminium hydroxy sulphate minerals. European Journal of Soil Science 49, 669–681.
| Crossref | GoogleScholarGoogle Scholar |
CAS |
van Breemen N
(1973) Dissolved aluminium in acid sulfate soils and in acid mine waters. Soil Science Society of America Proceedings 37, 694–697.
|
CAS |
van Breemen N
(1975) Acidification and deacidification of coastal plain soils as a result of periodic flooding. Soil Science Society of America Proceedings 39, 1153–1157.
|
CAS |
Vuai SA,
Nakamura K, Tokuyama A
(2003) Geochemical characteristics of runoff from acid sulfate soils in the northern area of Okinawa Island, Japan. Geochemical Journal 37, 579–592.
|
CAS |