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Methane emission from tidal freshwater marshes

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Abstract

In two tidal freshwater marshes, methane emission,production and accumulation in the pore-water have beenstudied. The two sites differ in their dominantvegetation, i.e., reed and bulrush, and in theirheights above sea level. The reed site was elevated inrelation to the bulrush site and had higher rates ofmethane emission and production. It is argued thatthis difference in methane emission between sites wasprimarily due to a different effect of reed andbulrush plants on methane dynamics rather than methaneoxidation related to tidal elevation. Methane emissionshowed strong seasonality related primarily to plantphysiology and only secondarily to temperature. Twocontrol sites at which vegetation was removedsystematically had lower emission rates indicating anoverall stimulating effect of plants on methaneemission from tidal marshes. Flooding reduced methaneemission, probably by blocking the primary sites ofmethane release in the lower part of the plantstems.

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References

  • Bartlett KB, Bartlett DS, Harriss RC & Sebacher DI (1987) Methane emissions along a salt marsh salinity gradient. Biogeochemistry 4: 183–202

    Google Scholar 

  • Berner (1980) Early Diagenesis – A Theoretical Approach. Princeton Univ. Press, Princeton

    Google Scholar 

  • Chanton JP & Dacey JWH (1991) Effects of vegetation on methane flux, reservoirs, and carbon isotopic composition. In: Sharkey T, Holland E & Mooney H (Eds) Trace Gas Emissions by Plants (pp 65–92). Academic Press, San Diego

    Google Scholar 

  • Chanton JP, Martens CS, Kelley CA, Crill PM & Showers WJ (1992) Methane transport mechanism and isotopic fractionation in emergent macrophytes of an Alaskan tundra lake. J. Geophys. Res. 97: 16,681–16,688

    Google Scholar 

  • Cicerone RJ & Oremland RS (1988) Biogeochemical aspects of atmospheric methane. Global Biogeochem. Cycles 2: 299–327

    Google Scholar 

  • Conrad R (1989) Control of methane production in terrestrial ecosystems. In: Andrea MO & Schimmel DS (Eds) Exchange of Trace Gases Between Terrestrial Ecosystems and the Atmosphere (pp 39–58). John Wiley & Sons, New York

    Google Scholar 

  • Dacey JWH & Klug MJ (1979) Methane emission from lake sediment through water lelies. Science 203: 1253–1255

    Google Scholar 

  • DeLaune RD, Smith CJ & Patrick Jr WH (1983) Methane release from Gulf coast wetlands. Tellus 35B: 8–15

    Google Scholar 

  • Denier van der Gon HAC & Breemen van N (1993) Diffusion-controlled transport of methane from soil to atmosphere as mediated by rice plants. Biogeochemistry 21: 177–190

    Google Scholar 

  • Fechner EJ & Hemond HF (1992) Methane transport and oxidation in the unsaturated zone of a Sphagnum peatland. Global Biogeochem. Cycles 6: 33–44

    Google Scholar 

  • Hesslein RH (1976) An in situ sampler for close interval pore water studies. Limnol. Oceanogr. 21: 912–914

    Google Scholar 

  • Holzapfel-Pschorn A & Seiler W (1986) Methane emission during a cultivation period from an Italian rice paddy. J. Geophys. Res. 91: 11,803–11,814

    Google Scholar 

  • Kelker D & Chanton J (1997) The effect of clipping on methane emission from Carex. Biogeochemistry 39: 37–44.

    Google Scholar 

  • Kelley CA, Martens CS & Ussler III W (1995) Methane dynamics across a tidally flooded riverbank margin. Limnol. Oceanogr. 40: 1112–1129

    Google Scholar 

  • Kelly CA & Chynoweth DP (1981) The contributions of temperature and of the input of organic matter in controlling rates of sediment methanogenesis. Limnol. Oceanogr. 26: 891–897

    Google Scholar 

  • King GM (1994) Associations of methanotrophs with the roots and rhizomes of aquatic vegetation. Appl. Environ. Microbiol. 60: 3220–3227

    Google Scholar 

  • King GM & Adamsen APS (1992) Effects of temperature on methane consumption in a forest soil and in pure cultures of the methanotroph Methylomonas rubra. Appl. Environ. Microbiol. 58: 2758–2763

    Google Scholar 

  • King GM & Wiebe WJ (1978) Methane release from soils of a Georgia salt marsh. Geochim. Cosmochim. Ac. 42: 343–348

    Google Scholar 

  • McAullife C (1971) GC determination of solutes by multiple phase equilibration. Chem. Technol. 1: 46–51

    Google Scholar 

  • Middelburg JJ, Klaver G, Nieuwenhuize J, Wielemaker A, Haas W de, Vlug T & Nat van der FJWA (1996) Organic matter mineralization in intertidal sediments along an estuarine gradient. Mar. Ecol. Prog. Ser. 132: 157–168

    Google Scholar 

  • Middelburg JJ, Nieuwenhuize J, Lubberts RK & van de Plascche O (1997) Organic carbon isotope systematics of coastal marshes. Est. Coast. Shelf Sci. 45: 681–687

    Google Scholar 

  • Minoda T & Kimura M (1996) Photosynthates as dominant source of CH4 and CO2 in soil water and CH4 emitted to the atmosphere from paddy fields. J. Geophys. Res. 101: 21,091–21,097

    Google Scholar 

  • Moore TR, Heyes A & Roulet NT (1994) Methane emissions from wetlands, southern Hudson Bay lowland. J. Geophys. Res. 99: 1455–1467

    Google Scholar 

  • Morrissey LA & Livingston GP (1992) Methane emissions from Alaska arctic tundra: An assessment of local spatial variability. J. Geophys. Res. 97: 16,661–16,670

    Google Scholar 

  • Van der Nat FJWA, de Brouwer JFC, Middelburg JJ & Laanbroek HJ (1997) Spatial distribu-tion and inhibition by ammonium of methane oxidation in intertidal freshwater marshes. Appl. Environ. Microbiol. 63: 4,734–4,740

    Google Scholar 

  • Van der Nat FJWA & Middelburg JJ (1998a) Seasonal variation in methane oxidation by the rhizosphere of Phragmites australis and Scirpus lacustris. Aquatic Botany 61: 95–110

    Google Scholar 

  • Van der Nat FJWA & Middelburg JJ (1998b) Effects of two common macrophytes on methane dynamics in freshwater sediments. Biogeochem. 43: 79–104

    Google Scholar 

  • Van der Nat FJWA, Middelburg JJ, van Meeteren D & Wielemakers A (1998) Diel methane emission patterns from Scirpus lacustris and Phragmites australis. Biogeochem. 41: 1–22

    Google Scholar 

  • Nieuwenhuize J, Maas YEM & Middelburg JJ (1994) Rapid analysis of organic carbon and nitrogen in particulate materials. Mar. Chem. 45: 217–224

    Google Scholar 

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

    Google Scholar 

  • Roden EE & Wetzel RG (1996) Organic carbon oxidation and surpression of methane produc-tion by microbial Fe(III) oxide reduction in vegetated and unvegetated freshwater wetland sediments. Limnol. Oceanogr. 41: 1733–1748

    Google Scholar 

  • Roulet NT, Rosemary A & Moore TR (1992) Low boreal wetlands as a source of atmospheric methane. J. Geophys. Res. 97: 3739–3749

    Google Scholar 

  • Sass RL, Fisher FM & Harcombe PA (1990) Methane production and emission in a Texas rice field. Global Biogeochem. Cycles 4: 47–68

    Google Scholar 

  • Schütz H, Schröder P & Rennenberg H (1991) Role of plants in regulating the methane flux to the atmosphere. In: Sharkey T, Holland E & Mooney H (Eds) Trace Gas Emissions by Plants (pp 29–63). Academic Press, San Diego.

    Google Scholar 

  • Schütz H, Seiler W & Conrad R (1989) Processes involved in formation and emission of methane in rice paddies. Biogeochemistry 7: 33–53

    Google Scholar 

  • Sebacher D, Harriss RC & Bartlett KB (1985) Methane emissions to the atmosphere through aquatic plants. J. Environ. Qual. 14: 40–46

    Google Scholar 

  • Shannon RD & White JR (1994) A Three-year study of controls on methane emissions from two Michigan peatlands. Biogeochemistry 27: 35–60

    Google Scholar 

  • Shannon RD, White JR, Lawson JE & Gilmour BS (1996) Methane efflux from emergent vegetation in peatlands. J. Ecol. 84: 239–246

    Google Scholar 

  • Whiting GJ & Chanton JP (1992) Plant-dependent CH4 emission in a subartic canadian fen. Global Biogeochem. Cycles 6: 225–231

    Google Scholar 

  • Whiting GJ & Chanton JP (1993) Primary production control of methane emission from wetlands. Nature 364: 794–795

    Google Scholar 

  • Whiting GJ, Chanton JP, Bartlett DS & Hapell JD (1991) Relationships between CH4 emission, biomass, and CO2 exchange in a subtropical grassland. J. Geophys. Res. 96: 13,067–13,071

    Google Scholar 

  • Wiesenburg DA & Guinasso NL (1979) Equilibrium solubilities of methane, carbon monoxide and hydrogen in water and seawater. J. Chem. Eng. Data 24: 356–360

    Google Scholar 

  • Wilson JO, Crill PM, Bartlett KB, Sebacher DI, Harriss RC & Sass RL (1989) Seasonal variation of methane emissions from a temperate swamp. Biogeochemistry 8: 55–71

    Google Scholar 

  • Yavitt JB, Lang GE & Downey DM (1988) Potential methane production and methane oxida-tion rates in peatland ecosystems of the Appalachian mountains, United states. Global Biogeochem. Cycles 2: 253–268.

    Google Scholar 

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Correspondence to Jack J. Middelburg.

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Van der Nat, FJ., Middelburg, J.J. Methane emission from tidal freshwater marshes. Biogeochemistry 49, 103–121 (2000). https://doi.org/10.1023/A:1006333225100

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