Discharged Sulfuric Acid from Peatland to River System

Abstract

In this chapter I first give an overview of environmental problems due to contamination by sulfuric acid of surface water systems. Then I specially focus on the sulfuric acid discharge from the acid sulfate soils in tropical peat swamps occurring after agricultural land development in Central Kalimantan, Indonesia. Pyrite-containing sediments can be found in several parts of the world ranging from tropical to Arctic and Antarctic regions. As long as these pyrite-containing sediments remain waterlogged or covered with other sediments without pyrite, the presence of pyrite does not constitute any danger to the environment. Drainage of water or removal of covering layers for agricultural or industrial purposes, however, enable oxygen to enter the pyrite-containing sediments, and subsequently pyrite is oxidized to produce sulfuric acid. One of the regional environmental problems caused by human activities affecting tropical peat swamp forests, especially destruction of peat soil due to agricultural land development, is the oxidation of pyrite within the sediment underneath the peat layer. In order to estimate the range of the area that is affected by the sulfuric acid pollution, the water chemistry of some rivers in Central Kalimantan was surveyed. The sulfuric acid loading from pyrite oxidation appeared from the river mouth up to 135 km upstream. The discharge of pyritic sulfate from peat soil to the limnological system is much higher in the high water table season (October to March) than in the low water table season. Control of pyrite oxidation is indispensable for maintaining sustainable land use of the tropical peat land.

Keywords

Acid sulfate soil Basin Canal Peat swamp Pyrite oxidation Sulfuric acid discharge 

Notes

Acknowledgement

Results shown in this paper were mainly obtained from SATREPS (Science and Technology Research Partnership for Sustainable Development) project entitled as “Wild fire and carbon management in peat-forest in Indonesia” founded by JST (Japan Science and Technology Agency) and JICA (Japan International Cooperation Agency).

References

  1. Andersen MS, Larsen F, Postma D (2001) Pyrite oxidation in unsaturated aquifer sediments, reaction stoichiometry and rate of oxidation. Environ Sci Technol 35:4074–4079CrossRefGoogle Scholar
  2. Anderson JAR (1983) The tropical peat swamps of western Malaysia. In: Gore AJP (ed) Ecosystems of the world 4B, mires: swamp, bog, fen and moor, regional studies. Elsevier Scientific Publishing, Amsterdam, pp 181–199Google Scholar
  3. Anisfeld SC, Benoit G (1997) Impacts of flow restrictions on salt marshes: an instance of acidification. Environ Sci Technol 31:1650–1657CrossRefGoogle Scholar
  4. Arkesteyn GJMW (1980) Pyrite oxidation in acid sulphate soils: the role of microorganisms. Plant Soil 54:119–134CrossRefGoogle Scholar
  5. Bachmann TM, Friese K, Zachmann DW (2001) Redox and pH conditions in the water column and in the sediments of an acidic mining lake. J Geochem Explor 73:75–86CrossRefGoogle Scholar
  6. Balkenhol R, Ludwig B, Ufer K, Jochum J, Friedrich G (2001) Pyrite oxidation in sediment samples from the German open-cut brown coal mine Zwenkau: mineral formation and dissolution of silicates. J Plant Nutr Soil Sci 164:283–288CrossRefGoogle Scholar
  7. Blunden B, Indraratna B, ASCE Member (2001) Pyrite oxidation model for assessing ground-water management strategies in acid sulfate soils. J Geotech Geoenviron Eng 127:146–157CrossRefGoogle Scholar
  8. Bottrell SH, Parkes RJ, Cragg BA, Raiswell R (2000) Isotopic evidence for anoxic pyrite oxidation and stimulation of bacterial sulphate reduction in marine sediments. J Geol Soc Lond 157:711–714CrossRefGoogle Scholar
  9. Caçador MI, Madureira MJ, Vale C (2000) Effects of plant roots on salt-marsh sediment geochemistry. In: Flemming BW, Delafontaine MT, Liebezeit G (eds) Muddy coast dynamics and resource management. Elsevier Science, Amsterdam, pp 197–204CrossRefGoogle Scholar
  10. Chabbi A (1999) Juncus bulbosus as a pioneer species in acid lignite mining lakes: interactions, mechanism and survival strategies. New Phytol 144:133–142CrossRefGoogle Scholar
  11. Clymo RS (1983) Peat. In: Gore AJP (ed) Ecosystems of the world 4A, mires: swamp, bog, fen and moor, general studies. Elsevier Scientific Publishing, Amsterdam, pp 159–224Google Scholar
  12. Collins B, McArthur JV, Sharitz RR (2004) Plant effects on microbial assemblages and remediation of acidic coal pile runoff in mesocosm treatment wetlands. Ecol Eng 23:107–115CrossRefGoogle Scholar
  13. de Haan SB, Rae JE, Parker A (1994) Pyrite oxidation in the tertiary sands of the London basin aquifer. Appl Geochem 9:161–173CrossRefGoogle Scholar
  14. Djuwansah M (1999) Some characteristics of podzols in Kalimantan. In: Iwakuma et al (ed) Tropical peat lands. Graduate School of Environmental Earth Science, Hokkaido University, Sapporo and Research and Development Center for Biology, Bogor, pp 33–37Google Scholar
  15. Evangelou VP, Zhang YL (1995) A review: pyrite oxidation mechanisms and acid mine drainage prevention. Crit Rev Environ Sci Technol 25:141–199CrossRefGoogle Scholar
  16. Haraguchi A (2007) Effect of sulfuric acid discharge on the river water chemistry in peat swamp forests in Central Kalimantan, Indonesia. Limnology 8:175–182CrossRefGoogle Scholar
  17. Haraguchi A, Shimada S, Takahashi H (2000) Distribution of peat and its chemical properties around Lahei in the catchment of the Mangkutup River, Central Kalimantan. Tropics 10:265–272CrossRefGoogle Scholar
  18. Haraguchi A, Akioka M, Shimada S (2005) Does pyrite oxidation contribute to the acidification of tropical peat? – a case study in a peat swamp forest in Central Kalimantan, Indonesia. Nutr Cycl Agroecosyst 71:101–108CrossRefGoogle Scholar
  19. Haraguchi A, Akioka M, Shimada S, Iyobe T (2006) Factors acidifying peat in Central Kalimantan, Indonesia. Tropics 15:397–401CrossRefGoogle Scholar
  20. Hines ME, Knollmeyer SL, Tugel JB (1989) Sulfate reduction and other sedimentary biogeochemistry in a northern New England salt marsh. Limnol Oceanogr 34:578–590CrossRefGoogle Scholar
  21. Howarth RW, Giblin A (1983) Sulfate reduction in the salt marshes at Sapelo Island, Georgia. Limnol Oceanogr 28:70–82CrossRefGoogle Scholar
  22. Howarth RW, Merkel S (1984) Pyrite formation and the measurement of sulfate reduction in salt marsh sediments. Limnol Oceanogr 29:598–608CrossRefGoogle Scholar
  23. Hsieh YP, Yang CH (1997) Pyrite accumulation and sulfate depletion as affected by root distribution in a Juncus (needle rush) salt marsh. Estuaries 20:640–645CrossRefGoogle Scholar
  24. Hüttl RF, Weber E (2001) Forest ecosystem development in post-mining landscapes: a case study of the Lusatian lignite district. Naturwissenschaften 88:322–329CrossRefGoogle Scholar
  25. Igarashi T, Hataya R, Oyama T (2003) Estimation of pyrite oxidation rate by sulfate ion discharged from a catchment. J Geochem Explor 77:151–165CrossRefGoogle Scholar
  26. Kargi F, Robinson JM (1982) Microbial desulfurization of coal by thermophilic microorganism Sulfolobus acidocaldarius. Biotechnol Bioeng 24:2115–2121CrossRefGoogle Scholar
  27. King GM (1983) Sulfate reduction in Georgia salt marsh soils: an evaluation of pyrite formation by use of 35S and 55Fe tracers. Limnol Oceanogr 28:987–995CrossRefGoogle Scholar
  28. King GM (1988) Patterns of sulfate reduction and the sulfur cycle in a South Carolina salt marsh. Limnol Oceanogr 33:376–390CrossRefGoogle Scholar
  29. Larsson L, Olsson G, Holst O, Karlsson HT (1990) Pyrite oxidation by thermophilic archaebacteria. Appl Environ Microbiol 56:697–701Google Scholar
  30. Lord CJ III, Church TM (1983) The geochemistry of salt marshes: sedimentary ion diffusion, sulfate reduction, and pyritization. Geochim Cosmochim Acta 47:1381–1391CrossRefGoogle Scholar
  31. Ludwig B, Khanna P, Balkenhol R, Friedrich G, Dohrmann R (1999) Pyrite oxidation in a sediment sample of an open-cut brown coal mine: mineral formation, buffering of acidity and modeling of cations and sulfate. J Plant Nutr Soil Sci 162:499–509CrossRefGoogle Scholar
  32. Luther GW III, Giblin A, Howarth RW, Ryans RA (1982) Pyrite and oxidized iron mineral phases formed from pyrite oxidation in salt marsh and estuarine sediments. Geochim Cosmochim Acta 46:2665–2669CrossRefGoogle Scholar
  33. MacKinnon K, Hatta G, Halim H, Mangalik A (1996) Wetland resource (chapter 10) In: The ecology of Kalimantan, Periplus Editions (HK), Singapore, pp 445–488Google Scholar
  34. Meyer G, Waschkies C, Hüttl RF (1999) Investigations on pyrite oxidation in mine spoils of the Lusatian lignite mining district. Plant Soil 213:137–147CrossRefGoogle Scholar
  35. Miley GA, Kiene RP (2004) Sulfate reduction and porewater chemistry in a Gulf Coast Juncus roemerianus (needlerush) marsh. Estuaries 27:472–481CrossRefGoogle Scholar
  36. Monterroso C, Macías F (1998) Drainage waters affected by pyrite oxidation in a coal mine in Galicia (NW Spain): composition and mineral stability. Sci Total Environ 216:121–132CrossRefGoogle Scholar
  37. Rasmussen K, Willems M (1981) Pyrite oxidation and leaching in excavated lignite soil. Acta Agric Scand 31:107–115CrossRefGoogle Scholar
  38. Rawlings DE, Tributsch H, Hansford GS (1999) Reasons why ‘Leptospirillum’-like species rather than Thiobacillus ferrooxidans are the dominant iron-oxidizing bacteria in many commercial processes for the biooxidation of pyrite and related ores. Microbiology 145:5–13CrossRefGoogle Scholar
  39. Ritsema CJ, Groenenberg JE (1993) Pyrite oxidation, carbonate weathering, and gypsum formation in a drained potential acid sulfate soil. Soil Sci Soc Am J 57:968–976CrossRefGoogle Scholar
  40. Schippers A, Jozsa P-G, Sand W, Kovacs ZM, Jelea M (2000) Microbiological pyrite oxidation in a mine tailings heap and its relevance to the death of vegetation. Geomicrobiol J 17:151–162CrossRefGoogle Scholar
  41. Tsaplina IA, Bogdanova TI, Sayakin DD, Karavaiko GI (1992) Effects of organic substances on the growth of Sulfobacillus thermosulfidooxidans and pyrite oxidation. Mikrobiologiya 60:34–40Google Scholar
  42. Vasander H, Tuittila ES, Lode E, Lundin L, Ilomets M, Sallantaus T, Heikkilä R, Pitkänen ML, Laine J (2003) Status and restoration of peatlands in northern Europe. Wetl Ecol Manag 11:51–63CrossRefGoogle Scholar
  43. Werner F, Bilek F, Luckner L (2001) Impact of regional groundwater flow on the water quality of an old post-mining lake. Ecol Eng 17:133–142CrossRefGoogle Scholar
  44. Wisotzky F, Obermann P (2001) Acid mine groundwater in lignite overburden dumps and its prevention – the Rhineland lignite mining area (Germany). Ecol Eng 17:115–123CrossRefGoogle Scholar
  45. Wu MM, Baltrus JP, Winschel RA (1990) Coal weathering: organic sulfur oxidation and the effects of pyrite oxidation on thermoplasticity. In: Marluszewski R, Wheelock TD (eds) Processing and utilization of high-sulfur coals III. Elsevier, Amsterdam, pp 745–755Google Scholar
  46. Zuoping Z, Hecai N, Gerke HH, Hüttl RF (1998) Pyrite oxidation related to pyritic minesite spoils and its controls: a review. Chin J Geochem 17:159–169CrossRefGoogle Scholar

Copyright information

© Springer Japan 2016

Authors and Affiliations

  1. 1.Faculty of Environmental EngineeringThe University of KitakyushuKitakyushuJapan

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