Effects of vascular plants on methane emissions from natural wetlands

Acta Ecologica Sinica

Volumn 25, Issue 12, 2005, Pages 3375-3382

  Duan, Xiao Nan ^a   Wang, Xiao Ke ^a   Ouyang, Zhi Yun ^a  

^a RESEARCH CENTER FOR ECO ENVIRONMENTAL SCIENCES   (China)

Author keywords

Methane; Natural wetland; Oxidation; Production; Transport; Vascular plant

Indexed keywords

BACTERIA (MICROORGANISMS); TRACHEOPHYTA;

EID: 30744445419     PISSN: 10000933     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Review

References (96)

1. Jugsujinda A, Delaune R D, Lindau C W, et al. Factors controlling carbon dioxide and methane production in acid sulfate soils. Water Air and Soil Pollution, 1996, 87: 345-355.
2. IPCC(Intergovernmental Panel on Climate Change). Climate Change 2001, The Scientific Basis. Cambridge: Cambridge University Press, 2001.
3. Houweling S, Kaminski T, Dentener F J, et al. Inverse modeling of methane sources and sinks using the adjoint of a global transport model, J. Geophys. Res. , 1999, 104(d21): 26137-26160.
4. Whiting G J, Chanton J P. Primary production control of methane emission from wetlands. Nature, 1993, 364: 794-795.
5. Whiting G J, Chanton J P. Plant-dependent CH4 emission in a subarctic Canadian fen. Global Biogeochemical Cycles, 1992, 6: 225-231.
6. Joabsson A, Christensen T R. Methane emissions from wetlands and their relationship with vascular plants: an Arctic example. Global Change Biology, 2001, 7: 919-932.
7. Shaver G R, Kummerow J. Phenology, resource allocation, and growth of arctic vascular plants. In: Chapin III F S, Jefferies R L, Roynolds J F, et al. eds. Arctic ecosystems in a changing climate: An ecophysiological perspective. San Diego: Academic Press, 1992. 193-212.
8. Joabsson A, Christensen T R, Wallen B. Vascular plant controls on methane emissions from northern peatforming wetlands. Trees, 1999, 14(10):385-388.
9. Chanton J P, Bauer J E, Glaser P A, et al. Radiocarbon evidence for the substrates supporting methane formation within northern Minnesota peatlands. Geochimica et Cosmochimica Acta, 1995, 59: 3663-3668.
10. King J Y, Reeburgh W S. A pulse-labeling experiment to determine the contribution of recent plant photosynthates to net methane emission in arctic wet sedge tundra. Soil Biology & Biochemistry, 2002, 34:173-180.
11. 2 releases from tundra soils in a changing climate. Applied Soil Ecology, 1999, 11:127-134.
12. 2 and water depth regulation of methane emissions: Comparison of woody and non-woody wetland plant species. Biogeochemistry, 2003, 63:117-134.
13. 4 in high latitude wetlands: measuring, modeling and predicting response to climate change. Polar Research, 1999, 18: 237-244.
14. Jones D L. organic acids in the rhizophere- a critical review. Plant and Soil, 1998, 205: 25-44.
15. Purvaja R, Ramesh R, Frenzel P. Plant-mediated methane emission from an Indian mangrove. Global Change Biology, 2004, 10: 1825-1834.
16. 2 to trace carbon metabolism from photosynthesis through methaogensis in a wetland plant-soil-atmosphere microcosm. Fourth symposium on Bio geochemistry of Wetlands, New Oreleans, UAS., 1996.
17. Ding W X, Cai Z C, Tsuruta H. Plants species on methane emissions from freshwater marshes. Atmospheric Envionment, 2005, 39: 3199-3207.
18. Juutinen S, Larmola T, Remus R, et al. The contribution of Phragmigtes australis litter to methane emission in planted and non-planted fen microcosms. Biol. Fertil. Soils, 2003, 38: 0-14.
19. 4 emissions from a northern peatland. Global Biogeochemical Cycles, 1999, 13: 81-91.
20. Ström L S, Ekberg A, Mastepannov M, et al. The effect of vascular plants on carbon turnover and methane emissions from a tundra wetland. Global Change Biology, 2003, 9:1185-1192.
21. Hornibrook E R C, Longstaffe W S, Fyfe W S. Spatial distribution of microbial methane production pathways in temperate zone wetland soils: stable carbon and hydrogen isotope evidence. Geochimica et Cosmoch mica Acta, 1997, 61:745-753.
22. Burdige D J. The biogeochemistry of manganese and iron reduction in marine sediments. Earth-Science Reviews, 1993, 35: 249-284.
23. Sundby B, Vale C, Cacador I, et al. Metal-rich concretions on the roots of salt-marsh plants: mechanisms and rate of formation. Limnology and Oceanography, 1998, 43: 245-252.
24. Achtnich C F, Rude P D. Competition for electron donors among nitrate reducers, ferric iron reducers, sulfate reducers, and methaogens in anoxic paddy soil. Biol. Fertil. Soils, 1988, 19: 65-72.
25. Middelburg J J, Klaver G, Nieuwenhuize J, et al. Organic matter mineralization in intertidal sediments along an estuarine gradient. Mar. Ecol. Prog. Ser. , 1996, 132: 157-168.
26. Rodden E E, Wetzel R G. Organic carbon oxidation and suppression of methane production by microbial Fe (III) oxide reduction in vegetated and unvegetated freshwater wetland sediments. Limnology and Oceanography, 1996, 41:1733-1748.
27. Van der Nat F J W A, Middelburg J J. Effects of two common macrophytes on methane dynamics in freshwater sediments. Biogeochemistry, 1998, 43:79-104.
28. 2 and Corg flux on diagenetic reaction balances. J. Mar. Res., 1994, 52:259-295.
29. Kludze H K, DeLaune R D. Straw application effects on methane and oxygen exchange and growth in rice. Soil Sci. Soc. Am. J., 1995, 59:824-830.
30. Thomas K L, Benstead J, Davies K L, et al. The role of wetland plants in the diurnal control of methane and carbon dioxide fluxes in peat. Soil Biology & Biochemistry, 1996, 28: 17-23.
31. Curl R, Truelove B. The Rhizosphere. New York: Springer, 1986.
32. King G M. Association of methanotrophs with the roots and rhizomes of aquatic vegetation. Applied and Environmental Microbiology, 1994,60: 3220-3227.
33. Schipper L A, Reddy K R. Methane oxidation in the rhizosphere of Dagittaria lancifolia. Soil. Soc. Am. J., 1996, 40: 611-616.
34. Van der Gon, H A C D. Neue, H U. Oxidation of methane in the rhizosphere of rice plants. Biol. Fertil. Soils, 1996, 22: 359-366.
35. Van der Nat F J W A, Middelburg J J. Seasonal variation in methane oxidation by the rhizosphere of Phragmites australis and Scirpus lacustris. Biogeochemistry, 1998, 43:79-104.
36. Caffrey J M, Kemp W M. Seasonal and spatial patterns of oxygen production, respiration and root-rhizome release in Potamogeton perfoliatus L. and Zostera marina L. Aquatic Batony, 1991, 40:109-128.
37. 4 oxidation: the activity of bacteria, their distribution and the microenvironment. Soil Biology & Biogeochemistry, 1998, 30: 1903-1916.
38. Happell J D, Chanton J P, Whiting G J, et al. Stable isotopes as tracers of methane dynamics in Everglades marshes with and without active populations of methane oxidizing bacteria. Journal of Geophysical Research, 1993, 98:14771-14782.
39. Lombardi J E, Epp M A, Chanton J P. Investigation of the methyl fluoride technique for determining rhizosphere methane oxidation. Biogeochemistry, 1997, 36: 153-172.
40. Sass R L, Fisher F M, Harcombe P A, et al. Methane production and emission in a Texas rice field. Global Biogeochemistry. Cycles, 1990, 4: 47-68.
41. Gerard G, Chanton J P. Quantification of methane oxidation in the rhizosphere of emergent aquatic macrophytes. Biogeochemistry, 1993, 23: 79-97.
42. Popp T J, Chanton J P, Whiting G J, et al. Evaluation of methane oxidation in the rhizosphere of a Carex dominated fen in north central Alberta, Canada. Biogeochemistry, 2000, 51: 259-281.
43. Frenzel P, Bosse U. Methyl fluoride, an inhibitor of methane oxidation and methane production. FEMS Microbiol. Ecol. , 1996, 21:25-36.
44. Gilbert B, Frenzel P. Methanotrophic bacteria in the rhizosphere of rice microcosms and their effect on pore water methane concertration and methane emission. Biol. Fertil. Soils. , 1995, 20: 93-100.
45. Epp M A, Chanton J P. Application of the methyl fluoride technique to the determination of rhizospheric methane oxidation. Journal of Geographysical Research, 1993, 98:18413-18422.
46. King G M. Ecological aspects of methane oxidation, a key determinate of global methane dynamics. In: Marshall K C ed. Advances in Microbial Ecology. New York: Plenum Press,1992. 431-468.
47. Schipper L A, Reddy K R. Methane oxidation in the rhizosphere of Dagittaria lancifolia. Soil. Soc. Am. J. , 1996, 40: 611-616.
48. Callhoun A, King G M. Regulation of root-associated methanotrophy by oxygen availability in the rhizosphere of two aquatic macrophytes. Applied and Environmental Microbiology, 1997, 63(8): 3051-3058.
49. Roslev R, King G M. Regulation of methane oxidation in a freshwater wetland by water table changes and anoxia. FEMS Microbiology Ecology, 1996, 19:105-155.
50. Crill P M, Martikainen P J, Nykanen H, et al. Temperature and N fertilization effects on methane oxidation in a drained peatland soil. Soil Biology and Biochemistry, 1994, 26(10): 1331-1339.
51. Van der Nat F J W A, deBrouwer J F C, Middelburg J J, et al. Spatial distribution and inhibition by ammonium of methane oxidation in intertidal freshwater marshes. Applied and Environmental Microbiology, 1997, 63(12): 4734-4740.
52. Bodelier P L E, Laanbroek H J. Nitrogen as a regulatory factor of methane oxidation in soils and sediments. FEMS Microbiology Ecology, 2004, 47: 265-277.
53. Granberg G, Sundh I, Svensson B H, et al. Effects of temperature and sulfur deposition on methane emission from a boreal mire. Ecology, 2001, 82: 1982-1998.
54. Boon P I, Kee K. Methane oxidation in sediments of a floodplain wetland in south-eastern Australia. Letters in Appled Microbiology, 1997, 25: 138-142.
55. Ding W X, Cai Z C, Tsuruta H. Summertime variation of methane oxidation in the rhizosphere of a Carex dominated freshwater marsh. Atmospheric Environment, 2004, 38: 4165-4173.
56. Dunfield P, Knowles R, Dumont R, et al. Methane production and consumption in temperate and subarctic peat soils: Response to temperature and pH. Soil Biology and Biochemistry,1993, 25(3):321-326.
57. Holzapfel-Pschorn A, Conrad R, Seiler W. Effects of vegetation on the emission of methane from submerged paddy soil. Plant and Soil, 1986, 92: 223-322.
58. Schimel J P. Plant transport and methane production as controls on methane flux from arctic wet meadow tundra. Biogeochemistry, 1995, 28: 183-200.
59. Kim J, Verma S B, Billebach D P. Seasonal variation in methane emission from a remperate Phragmites-dominated marsh, effect of growth stage and plant-mediated transport. Global Change Biology, 1998, 5: 433-440.
60. Chanton J P, Whiting G J. Methane stable isotopic distributions as indicators of gas transport mechanisms in emergent aquatic plants. Aquatic Botany, 1996, 54: 227-236.
61. Chanton J P, Whiting G J, Happell J D, et al. Contrasting rates and diurnal patterns of methane emission from emergent aquatic macrophytes. Aquatic Botany, 1993, 46:111-128.
62. Fyre J P, Mills A L, Odum W E. Methane flux in Peltandra virginica wetlands: comparison of field data with a mathematical model. Am. J. Bot. ,1994, 81: 407-413.
63. Van der Nat F J W A, Middelburg J J, van Meeteren D, et al. Diel methane emission patterns from Scirpus lacustris and Phragmites australis. Biogeochemistry, 1998, 41: 1-22.
64. Chanton J P, Decay J W H. Effects of vegetation on methane flux, reservoirs, and carbon isotopic composition. In: Sharkey T, Holland E, Mooney H, eds. Trace Gas Emissions by Plants. San Diego: Academic Press,1991. 65-92.
65. Armstrong J, Armstrong W, Beckett P M. Phragmites australis: Venturi- and Humidity- induced pressure flows enhance rhizome aeration and rhizosphere oxidation. New Phytol. , 1992, 120:197-207.
66. Sorrel B K, Boon P I. Convective gas flow in Eleocharis sphacelata R. Br: methane transport and release from wetlands. Aquatic Botany, 1994, 47:197-212.
67. Bendix M, Tornbjerg T, Brix H. Internal gas transport in Typha latifolia and Typha angustifolia L 1. Humidity-induced pressurization and convective throughflow. Aquatic Botany, 1994, 49: 75-89.
68. Brix H, Sorrel B K, Schierup H. Internal pressurization and convective gas flow in some emergent freshwater macrophytes. Limnology and Oceanography, 1992, 37: 1420-1433.
69. Arkebauer T J, Chanton J P, Verma S B, et al. Field measurementsof internal pressurization in Phragmites australis(Poaceae) and implications for regulation of methane emissions in a Midlatitude Prairie Wetland. American Journal of Botany, 2001, 88(4): 653-658.
70. Yavitt J B, Knapp A K. Aspects of methane flow from sediment through emergent cattail(Typha latifolia) plants. New phytologist, 1998, 139:495-503.
71. Arkebauer T J, Chanton J P, Verma S B, et al. Field measurementsof internal pressurization in Phragmites australis(Poaceae) and implications for regulation of methane emissions in a Midlatitude Prairie Wetland. American Journal of Botany, 2001, 88(4): 653-658.
72. Sebacher D I, Harriss R C, Bartlett K B. Methane emissions to the atmosphere through aquatic plants. Journal of Environmental Quality,1985, 14: 40-46.
73. Whitng G J, Chanton J P. Control of the diurnal pattern of methane emission from emergent aquatic macrophytes by gas transport mechanism. Aquatic Botany, 1996, 54:237-253.
74. Nouchi I, Mariko S, Aoki K. mechanism of methane transport from the rhizosphere to the atmosphere through rice plants. Plant Physiol. , 1990, 94: 59-66.
75. Harden H S, Chanton J P. Locus of methane release and mass-dependent fractionation from two wetland macrophytes. Limnology and Oceanography,1994, 39: 148-154.
76. Torn M S, Chapin F S. Environmental and biotic controls over methane flux from arctic tundra. Chemosphere, 1993, 26: 357-368.
77. Kelker D, Chanton J. The effect of clipping on methane emissions from Carex. Biogeochemistry, 1997, 39: 37-44.
78. Käki T, Ojala A, Kankaala P. Diel variation in methane emissions from stands of Phragmites australis(Cav.) Trin ex Steud. and Typha latifolia L. in a boreal lake. Aquatic Botany, 2001, 71: 259-271.
79. Knapp A K, Yavitt J B. Evaluation of a closed-chamber method for estimating emissions from aquatic plants. Tellus, 1992, 44: 64-71.
80. Morrissey L A, Zobel D B, Livingston G P. Significance of stomatal control on methane release form Carex-dominated wetlands. Chemosphere, 1993, 26: 339-355.
81. Ding W X, Cai Z C. Effect of plants on methane production,oxidation and emission. Chinese Journal of Applied Ecology, 2003,14(8): 1379-1384.
82. Fechner-Levy E J, Hemond H F. Trapped methane volume and potential effects on methane ebullition in a northern peatland. Limnology and Oceanography, 1996, 41(7): 1375-1383.
83. Minoda T, Kimura M. Contribution of photosynthesized carbon to the methane emitted from paddy fields. Geophys. Res. Lett. , 1994, 21:2007-2010.
84. Ding W D, Cai Z C, Tsuruta H. Diel variation in methane emissions from the stands of Carex lasiocarpa and Deyeuxia angustifolia in a cool temperate freshwater marsh. Atmospheric Environment, 2004, 38:181-188.
85. Grünfeld S, Brix H. Methanogesis and methane emissions, effects of water table, substrate type and presence of Phragmites australis. Aquatic Botany, 1999, 64: 63-75.
86. Kohl J G, Henze R, Kühl H. Evaluation of the ventilation resistance to convective gas-flow in the rhizomes of natural reed beds of Phragmites australis(Cav.) Trin. ex Steud. Aquatic Botany, 1996, 54:199-210.
87. Bartlett K B,Harriss R C. Review and assessment of methane emissions from wetlands. Chemosphere,1993, 26:261-320.
88. 4 exchange on the developmental topography of a peatland. Global Biogeochemical Cycles, 1996, 10: 233-245.
89. Van den Pol-van Dasselaar A, van Beusichem M L, Oenema O. Methane emissions from wet grasslands on peat soil in a nature preserve. Biogeochemistry,1998, 44: 205-220.
90. Bubier J L, Moore T R, Roulet N T, et al. Methane emissions from wetlands in the midboreal region of northern Ontario, Canada. Ecology, 1993,74: 2240-2254.
91. 2 from wetland ponds on the Hudson Bay(Hbls), J. Geophys. Res.-Atmos. , 1994, 99: 1495-1510.
92. Shannon R D, White J R. 3-year study of controls on methane emissions from 2 Michigan peatlands. Biogeochemisty, 1994, 27: 35-60.
93. King J Y, Reeburgh W S, Regli S K. Methane emission and transport by arctic sedges in Alaska: Results of a vegetation removal experiment. Journal of Geophysical Research, 1998, 103: 29083-29092.
94. Melack J M, Hess L, Gastil M, et al. Regionalization of methane emissions in the Amazon Basin with microwave remote sensing. Global Change Biology, 2004, 530-544.
95. Turunen J, Pitkänen A, Tahvanainen T, et al. Carbon accumulation in West Siberian mires, Russia. Global Biogeochemical Cycles, 2001, 15: 285-296.
96. 4 fluxes in an alpine turdra ecosystem. Bigogeochemistry,1999, 45: 243-264.