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Effects of vegetation on the emission of methane from submerged paddy soil

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Summary

Methane emission rates from rice-vegetated paddy fields followed a seasonal pattern different to that of weed-covered or unvegetated fields. Presence of rice plants stimulated the emission of CH4 both in the laboratory and in the field. In unvegetated paddy fields CH4 was emitted almost exclusively by ebullition. By contrast, in rice-vegetated fields more than 90% of the CH4 emission was due to plant-mediated transport. Rice plants stimulated methanogenesis in the submerged soil, but also enhanced the CH4 oxidation rates within the rhizosphere so that only 23% of the produced CH4 was emitted. Gas bubbles in vegetated paddy soils contained lower CH4 mixing ratios than in unvegetated fiels. Weed plants were also efficient in mediating gas exchnage between submerged soil and atmosphere, but did not stimulate methanogenesis. Weed plants caused a relatively high redox potential in the submerged soil so that 95% of the produced CH4 was oxidized and did not reach the atmosphere. The emission of CH4 was stimulated, however, when the cultures were incubated under gas atmospheres containing acetylene or consisting of O2-free nitrogen.

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References

  1. Baker-Blocker A, Donahue T M and Mancy K H 1977 Methane flux from wetland areas. Tellus 29, 245–250.

    CAS  Google Scholar 

  2. Barber D A, Ebert M and Evans N T S 1962 The movement of15O2 through barley and rice plants. J. Expt. Bot. 13, 397–403.

    CAS  Google Scholar 

  3. Cicerone R J and Shetter J D 1981 Sources of atmospheric methane: measurements inrice paddies and discussion. J. Geophys. Res. 96, 7203–7209.

    Google Scholar 

  4. Cicerone R J, Shetter J D and Delwiche C C 1983 Seasonal variation of methane flux from a California rice paddy. J. Geophys. Res. 88, 11022–11024.

    CAS  Google Scholar 

  5. Dacey J W H 1980 Internal winds in water lilies: an adaptation for life in anaerobic sediments. Science 210, 1017–1019.

    Google Scholar 

  6. Dacey J W H 1981 Pressurized ventilation in the yellow waterlity. Ecology 62, 1137–1147.

    Google Scholar 

  7. Dacey J W H and Klug M J 1979 Methane efflux from lake sediments through water lilies. Science 203, 1253–1255.

    CAS  Google Scholar 

  8. DeBont J A M, Lee K K and Bouldin D F 1978 Bacterial oxidation of methane in rice paddy. Ecol. Bull. (Stockholm) 26, 91–96.

    Google Scholar 

  9. DeBont J A M and Mulder E G 1976 Invalidity of the acetylene reduction assay in alkaneutilizing nitrogen-fixing bacteria. Appl. Environ. Microbiol. 31, 640–647.

    CAS  Google Scholar 

  10. Ehhalt D H and Schmidt U 1978 Sources and sinks of atmospheric methane. Pageoph 116, 452–464.

    Article  CAS  Google Scholar 

  11. Hale M G, Foy C L and Shay F J 1971 Factors affecting root exudation Adv. Agron. 23, 89–109.

    CAS  Google Scholar 

  12. Hale M G and Moore L D 1979 Factors affecting root exudation II: 1970–1978. Adv. Agron. 31, 93–124.

    CAS  Google Scholar 

  13. Hanson R S 1980 Ecology and diversity of methylotrophic organisms. Adv. Appl. Microbiol. 26, 3–39.

    CAS  Google Scholar 

  14. Harrison W H and Aiyer P A S 1913 The gases of swamp soils. Mem. Dept. Agr. Ind. 3, 65–04.

    Google Scholar 

  15. Higuchi T 1982 Gaseous carbon dioxide transport through the aerenchyma and intercellular spaces in relation to the uptake of carbon dioxide by rice roots. Soil Sci. Plant Nutr. (Tokyo) 28, 491–497.

    CAS  Google Scholar 

  16. Higuchi T, Yoda K and Tensho K 1984 Further evidence for gaseous CO2 transport in relation to root uptake of CO2 in rice plant. Soil Sci. Plant Nutr. (Tokyo) 30, 125–136.

    CAS  Google Scholar 

  17. Holzapfel-Pschorn A, Conrad R and Seiler W 1985 Production, oxidation and emission of methane from rice paddies. FEMS Microbiol. Ecol. In press.

  18. Jones J G and Simon B M 1981 Differences in microbial decomposition processes in profundal and littoral lake sediments, with particular reference to the nitrogen cycle. J. Gen. Microbiol. 123, 297–312.

    CAS  Google Scholar 

  19. Koyama T 1964 Biogeochemical studies on lake sediments and paddy soils and the production of atmospheric methane and hydrogen.In Recent Researches in the Fields of Hydrosphere, Atmosphere and Nuclear Geochemistry. Eds. Y Miyake and T Koyama. pp 143–177. Tokyo.

  20. Kozuchowski J and Johnson D L 1978 Gaseous emissions of mercury from an aquatic vascular plant. Nature 274, 468–469.

    Article  CAS  Google Scholar 

  21. Lee K K, Holst R W, Watanabe I and App A 1981 Gas transport through rice. Soil Sci. Plant Nutr. (Tokyo) 27, 151–158.

    CAS  Google Scholar 

  22. Mah R A and Smith M R 1981 The methanogenic bacteria.In The Prokaryotes, vol. 1. Eds. M P Starr, H Stolp, H G Trüper, A Balows and H G Schlegel. pp 948–977. Berlin.

  23. Nedwell D B 1984 The input and mineralization of organic carbon in anaerobic aquatic sediments. Adv. Microb. Ecol. 7, 93–131.

    CAS  Google Scholar 

  24. Raimbault M, Rinaudo G, Garcia J L and Boureau M 1977 A device to study metabolic gases in the rice rhizosphere. Soil Biol. Biochem. 9, 193–196.

    Article  CAS  Google Scholar 

  25. Rasmussen R A and Khalil M A K 1981 Atmospheric methane (CH4): trends and seasonal cycles. J. Geophys. Res. 86, 9826–9832.

    CAS  Google Scholar 

  26. Robinson W O 1930 Some chemical phases of submerged soil conditions. Soil Sci. 30, 197–217.

    CAS  Google Scholar 

  27. Rovira A D 1965 Plant root exudates and their influence upon soil microorganisms.In Ecology of Soil-Borne Plant Pathogens. Eds. K F Baker and W Snyder. pp 170–186. Berkeley.

  28. Rovira A D and Davey C B 1974 Biology of the rhizosphere.In The Plant Root and Its Environment. Ed E W Carosu. pp 153–204. Charlottesville.

  29. Rudd J W M and Taylor C D 1980 Methane cycling in aquatic environments. Adv. Aquat. Microbiol. 2, 77–150.

    CAS  Google Scholar 

  30. Sebacher D I, Harriss R C and Bartlett K B 1985 Methane emissions to the atmosphere through aquatic plants. J. Environ. Qual. 14, 40–46.

    CAS  Google Scholar 

  31. Seiler W 1984 Contribution of biological processes to the global budget of CH4 in the atmosphere.In Current Perspectives in Microbial Ecology. Eds. M J Klug and C A Reddy. pp 468–477. Washington D.C.

  32. Seiler W, Holzapfel-Pschorn A, Conrad R and Scharffe D 1984 Methane emission from rice paddies. J. Atmos. Chem. 1, 241–268.

    Article  CAS  Google Scholar 

  33. Sheppard J C, Westberg H, Hopper J F, Ganesan K and Zimmerman P 1982 inventory of global methane sources and their production rates. J. Geophys. Res. 87, 1305–1312.

    CAS  Google Scholar 

  34. Takai Y 1970 The mechanism of methane fermentation in flooded paddy soil. Soil Sci. Plant Nutr. (Tokyo) 16, 238–244.

    CAS  Google Scholar 

  35. Van Raalte M H 1941 On the oxygen supply of rice roots. Ann. Bot. Gard. Buitenzorg 51, 43–57.

    Google Scholar 

  36. Tanabe U and Sati J (1967) Effect of temperature on the decomposition of organic substances in flooded soil. Soil Sci. Plant. Nutr. (Tokyo) 13, 94–100.

    Google Scholar 

  37. Zehnder A J B 1978 Ecology of methane formation.In Water Pollution Microbiology, vol. 2, Ed R Mitchell, pp 349–376. New York.

  38. Zeikus J G 1983 Metabolic communication between biodegradative populations in nature.In Microbes in Their Natural Environments. Eds. J H Slater, R Whittenbury and J W T Wimpenny, pp 423–462. Cambridge U K.

  39. Zeikus J G and Winfrey M R 1976 Temperature limitation of methanogenesis in aquatic sediments. Appl. Environ. Microbiol. 31, 99–107.

    CAS  PubMed  Google Scholar 

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Authors and Affiliations

  1. Max-Planck-Institut für Chemie, Saarstr. 23, D-6500, Mainz, FRG

    A. Holzapfel-Pschorn, R. Conrad & W. Seiler

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  1. A. Holzapfel-Pschorn
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  2. R. Conrad
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  3. W. Seiler
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Holzapfel-Pschorn, A., Conrad, R. & Seiler, W. Effects of vegetation on the emission of methane from submerged paddy soil. Plant Soil 92, 223–233 (1986). https://doi.org/10.1007/BF02372636

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  • DOI: https://doi.org/10.1007/BF02372636

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