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Wetlands

pp 1–13 | Cite as

Effects of Environmental Variables on Spatiotemporal Variations of Nitrous Oxide Fluxes in the Pristine Riparian Marsh, Northeast China

  • Liquan Song
  • Yunlong Yao
  • Weifeng Gao
  • Tijiu Cai
  • Qingbo Wang
  • Dongfeng Fu
  • Xiaoxin Sun
  • Hong LiangEmail author
  • Dawen GaoEmail author
Wetlands and Climate Change

Abstract

Nitrous oxide (N2O) is an important greenhouse gas, and the riparian marsh plays an important role in modulating atmospheric concentrations of N2O. To investigate the effects of environmental variables on spatiotemporal variations of N2O fluxes in the pristine riparian marsh, the static chamber-GC techniques were used to explore the spatiotemporal variations of N2O fluxes in Calamagrostis angustifolia swamp meadow marsh (CASMM), Ecotone wetland (EW) and Carex Schmidtii Meinsh. marsh (CSMM) along the pristine riparian in Sanjiang Plain during one year. During non-growing season (October, 2015 to April, 2016), the variability of N2O fluxes in the three marshes were not significantly different (P > 0.05). However, during growing season (May to October, 2016), both variability differences of N2O fluxes between CSMM and EW, and between CSMM and CASMM were significant (P < 0.01). Atmospheric temperature, soil NH4+-N content and soil volumetric moisture content were the driving factors during non-growing season. During growing season, soil NH4+-N and NO3-N content were the driving factors among interactions of multiple environmental variables. CASMM and EW became the sinks of N2O during non-growing season but converted to the source of N2O during growing season. However, CSMM became all sink of N2O during every season.

Keywords

Nitrous oxide (N2O) Spatiotemporal variations Driving factors Pristine riparian marsh Sanjiang plain 

Notes

Acknowledgements

The present study was gratefully supported by the National Natural Science Foundation of China (Grant No. 31470543), National Natural Science Foundation for Youth Science of China (Grant No. 41301081). We sincerely thank Heilongjiang Sanjiang Plain Wetland Ecosystem Research Station and Heilongjiang Sanjiang National Nature Reserve Authority, in Fuyuan City, Heilongjiang Province, China. Grateful thanks to Lin Lin (The Department of Public Foreign Language, Jiamusi University, China) for her fruitful helps.

References

  1. Armstrong W (1980) Aeration in higher plants. Advances in Botanical Research 7:225–332CrossRefGoogle Scholar
  2. Audet J, Hoffmann CC, Andersen PM, Baattrup-Pedersen A, Johansen JR, Larsen SE, Kjaergaard C, Elsgaard L (2014) Nitrous oxide fluxes in undisturbed riparian wetlands located in agricultural catchments: emission, uptake and controlling factors. Soil Biology and Biochemistry 68:291–299CrossRefGoogle Scholar
  3. Bandibas J, Vermoesen A, Degroot C, Cleemput OV (1994) The effect of different moisture regimes and soil characteristics on nitrous oxide emission and consumption by different soils. Soil Science 158:106–114CrossRefGoogle Scholar
  4. Blicher-Mathiesen G, Hoffmann CC (1999) Denitrification as a sink for dissolved nitrous oxide in a freshwater riparian fen. Journal of Environmental Quality 28:257–262CrossRefGoogle Scholar
  5. Bremner JM, Blackmer AM (1979) Effects of acetylene and soil water content on emission of nitrous oxide from soils. Nature 280:380–381CrossRefGoogle Scholar
  6. Bussell, J., D. L. Jones, J. R. Healey and A. S. Pullin (2010) How do draining and re-wetting affect carbon stores and greenhouse gas fluxes in peatland soils ? Collaboration for Environmental Evidence Systematic Review CEE 08–012 (SR 49)Google Scholar
  7. Christensen S, Tiedje J (1990) Brief and vigorous N2O production by soil at spring thaw. Journal of Soil Science 41:1–4CrossRefGoogle Scholar
  8. Conrad R (1996) Soil microorganisms as controllers of atmospheric trace gases (H2, CO, CH4, OCS, N2O, and NO). Microbiological Reviews 60:609–640PubMedPubMedCentralGoogle Scholar
  9. Dalal RC, Wang W, Robertson GP, Parton WJ (2003) Nitrous oxide emission from Australian agricultural lands and mitigation options: a review. Australian Journal of Soil Research 41:165–195CrossRefGoogle Scholar
  10. Davidson EA, Janssens IA (2006) Temperature sensitivity of soil carbon decomposition and feedbacks to climate change. Nature 440:165–173CrossRefGoogle Scholar
  11. Davidson, E. A. and J. P. Schimel (1995) Microbial processes of production and consumption of nitric oxide, nitrous oxide, and methane. In: Matson, P., Harriss, R. (Eds.), Methods in ecology: trace gases. Blackwell Scientific:327–357Google Scholar
  12. Dhondt K, Boeckx P, Hofman G, Van Cleemput O (2004) Temporal and spatial patterns of denitrification enzyme activity and nitrous oxide fluxes in three adjacent vegetated riparian buffer zones. Biology and Fertility of Soils 40:243–251CrossRefGoogle Scholar
  13. Duxbury JM, Bouldin DR, Terry RE, Tate Iii RL (1982) Emissions of nitrous oxide from soils. Nature 298:462–464CrossRefGoogle Scholar
  14. Falkowski PG, Fenchel T, Delong EF (2008) The microbial engines that drive Earth's biogeochemical cycles. Science 320:1034–1039CrossRefGoogle Scholar
  15. Firestone M, Davidson E (1989) Microbiological basis of NO and N2O production and consumption in soil. Exchange of trace gases between terrestrial ecosystems and the. Atmosphere:7–21Google Scholar
  16. Firestone M, Firestone R, Tiedje J (1980) Nitrous oxide from soil denitrification: factors controlling its biological production. Science 208:749–751CrossRefGoogle Scholar
  17. Freeman C, Lock AM, Hughes S, Reynolds B (1997) Nitrous oxide emissions and the use of wetlands for water quality amelioration. Environmental Science & Technology 31:2438–2440CrossRefGoogle Scholar
  18. Goreau TJ, Kaplan WA, Wofsy SC, Mcelroy MB, Valois FW, Watson SW (1980) Production of NO2 and N2O by nitrifying Bacteria at reduced concentrations of oxygen. Applied and Environmental Microbiology 40:526–532PubMedPubMedCentralGoogle Scholar
  19. Groffman PM, Brumme R, Butterbach-Bahl K, Dobbie KE, Mosier AR, Ojima D, Papen H, Parton WJ, Smith KA, Wagner-Riddle C (2000) Evaluating annual nitrous oxide fluxes at the ecosystem scale. Global Biogeochemical Cycles 14:1061–1070CrossRefGoogle Scholar
  20. Hefting MM, Bobbink R, de Caluwe H (2003) Nitrous oxide emission and denitrification in chronically nitrate-loaded riparian buffer zones. Journal of Environmental Quality 32:1194–1203CrossRefGoogle Scholar
  21. Hefting MM, Bobbink R, Janssens MP (2006) Spatial variation in denitrification and N2O emission in relation to nitrate removal efficiency in a N-stressed riparian buffer zone. Ecosystems 9:550–563CrossRefGoogle Scholar
  22. Hernandez ME, Mitsch WJ (2006) Influence of hydrologic pulses, flooding frequency, and vegetation on nitrous oxide emissions from created riparian marshes. Wetlands 26:862–877CrossRefGoogle Scholar
  23. Hooper AB, Vannelli T, Bergmann DJ, Arciero DM (1997) Enzymology of the oxidation of ammonia to nitrite by bacteria. Antonie Van Leeuwenhoek 71:59–67CrossRefGoogle Scholar
  24. Hou C, Song C, Li Y, Wang J, Song Y, Wang X (2013) Effects of water table changes on soil CO2, CH4 and N2O fluxes during the growing season in freshwater marsh of Northeast China. Environment and Earth Science 69:1963–1971CrossRefGoogle Scholar
  25. Jacinthe PA, Bills JS, Tedesco LP, Barr RC (2012) Nitrous oxide emission from riparian buffers in relation to vegetation and flood frequency. Journal of Environmental Quality 41:95–105CrossRefGoogle Scholar
  26. Jiang C, Wang Y, Hao Q, Song C (2009) Effect of land-use change on CH4 and N2O emissions from freshwater marsh in Northeast China. Atmospheric Environment 43:3305–3309CrossRefGoogle Scholar
  27. Jørgensen CJ, Elberling B (2012) Effects of flooding-induced N2O production, consumption and emission dynamics on the annual N2O emission budget in wetland soil. Soil Biology and Biochemistry 53:9–17CrossRefGoogle Scholar
  28. Jørgensen C, Struwe S, Elberling B (2012) Temporal trends in N2O flux dynamics in a Danish wetland-effects of plant-mediated gas transport of N2O and O2 following changes in water level and soil mineral-N availability. Global Change Biology 18:210–222CrossRefGoogle Scholar
  29. Juszczak R, Augustin J (2013) Exchange of the greenhouse gases methane and nitrous oxide between the atmosphere and a temperate peatland in Central Europe. Wetlands 33:895–907CrossRefGoogle Scholar
  30. Kliewer BA, Gilliam JW (1995) Water-table management effects on denitrification and nitrous-oxide evolution. Soil Science Society of America Journal 59:1694–1701CrossRefGoogle Scholar
  31. Koch O, Tscherko D, Kandeler E (2007) Temperature sensitivity of microbial respiration, nitrogen mineralization, and potential soil enzyme activities in organic alpine soils. Global Biogeochemical Cycles 21:GB4017CrossRefGoogle Scholar
  32. Kowalchuk G, Stephen J (2001) Ammonia-oxidizing bacteria: a model for molecular microbial ecology. Annual Review of Microbiology 55:485–529CrossRefGoogle Scholar
  33. Liu L, Greaver TL (2009) A review of nitrogen enrichment effects on three biogenic GHGs: the CO2 sink may be largely offset by stimulated N2O and CH4 emission. Ecology Letters 12:1103–1117CrossRefGoogle Scholar
  34. Liu X, Ma X (2000) Influence of large-scale reclamation on natural environment and regional environmental protection in the Sanjiang plain. Scientia Geographica Sinica 20:14–19 (in Chinese)Google Scholar
  35. Liu X, Ma X (2002) Natural environmental change and ecological protection in the Sanjiang Plain. Science Press, Beijing, pp 59–65Google Scholar
  36. Lohila A, Aurela M, Hatakka J, Pihlatie M, Minkkinen K, Penttilä T, Laurila T (2010) Responses of N2O fluxes to temperature, water table and N deposition in a northern boreal fen. European Journal of Soil Science 61:651–661CrossRefGoogle Scholar
  37. Maag M, Vinther FP (1996) Nitrous oxide emission by nitrification and denitrification in different soil types and at different soil moisture contents and temperatures. Applied Soil Ecology 4:5–14CrossRefGoogle Scholar
  38. Machefert SE, Dise NB (2004) Hydrological controls on denitrification in riparian ecosystems. Hydrology and Earth System Sciences 8:686–694CrossRefGoogle Scholar
  39. Mistch WJ, Gosselin JG (2000) Wetlands[M ]. Van Nostrand Reinhold Company Inc., New York, pp 89–125Google Scholar
  40. Nag SK, Liu R, Lal R (2017) Emission of greenhouse gases and soil carbon sequestration in a riparian marsh wetland in Central Ohio. Environmental Monitoring and Assessment 189:580CrossRefGoogle Scholar
  41. Naiman RJ, Decamps H, McClain ME (2005) Riparia: ecology, conservation, and management of streamside communities. Elsevier Academic Press, OxfordGoogle Scholar
  42. Nastri A, Toderi G, Bernati E, Govi G (2000) Ammonia volatilization and yield response from urea applied to wheat with urease (NBPT) and nitrification (DCD) inhibitors. Agrochimica 44:231–239Google Scholar
  43. Poth M, Focht DD (1985) 15N kinetic analysis of N2O production by Nitrosomonas europaea: an examination of nitrifier denitrification. Applied and Environmental Microbiology 49:1134–1141PubMedPubMedCentralGoogle Scholar
  44. Ravishankara A, Portmann R (2009) Nitrous oxide (N2O): the dominant ozone-depleting substance emitted in the 21st century. Science 326:123–125CrossRefGoogle Scholar
  45. Repo ME, Susiluoto S, Lind SE, Jokinen S, Elsakov V, Biasi C, Virtanen T, Martikainen PJ (2009) Large N2O emissions from cryoturbated peat soil in tundra. Nature Geoscience 2:189–192CrossRefGoogle Scholar
  46. Ritchie GA, Nicholas DJD (1972) Identification of the sources of nitrous oxide produced by oxidative and reductive processes in Nitrosornonas europea. The Biochemical Journal 126:1181–1191CrossRefGoogle Scholar
  47. Seitzinger SP, Pilson MEO, Watson SW (1983) Nitrous oxide production in nearshore marine sediments. Science 222:1244–1245CrossRefGoogle Scholar
  48. Smith KA (1990) Greenhouse gas fluxes between land surfaces and the atmosphere. Progress in Physical Geography 14:349–372CrossRefGoogle Scholar
  49. Sommerfeld R, Mosier A, Musselman R (1993) CO2, CH4 and N2O flux through a Wyoming snowpack and implications for global budgets. Nature 361:140–142CrossRefGoogle Scholar
  50. Song C, Wang Y, Wang Y, Zhao Z (2005) Dynamics of CO2,CH4 and N2O emission fluxes from mires during freezing and thawing season. Environmental Sciences 26:7–12Google Scholar
  51. Song C, Zhang J, Wang Y, Wang Y, Zhao Z (2008) Emission of CO2, CH4 and N2O from freshwater marsh in northeast of China. Journal of Environmental Management 88:428–436CrossRefGoogle Scholar
  52. Song C, Xu X, Tian H, Wang Y (2009) Ecosystem-atmosphere exchange of CH4 and N2O and ecosystem respiration in wetlands in the Sanjiang plain, northeastern China. Global Change Biology 15:692–705CrossRefGoogle Scholar
  53. Stevens RJ, Laughlin RJ, Malone JP (1997) Measuring the contributions of nitrification and denitrification to the flux of nitrous oxide from soil. Soil Biology and Biochemistry 29:139–151CrossRefGoogle Scholar
  54. Sun Z, Wang L, Mou X, Jiang H, Sun W (2014) Spatial and temporal variations of nitrous oxide flux between coastal marsh and the atmosphere in the Yellow River estuary of China. Environmental Science and Pollution Research International 21:419–433CrossRefGoogle Scholar
  55. Syakila A, Kroeze C (2011) The global nitrous oxide budget revisited. Greenhouse Gas Measurement and Management 1:17–26CrossRefGoogle Scholar
  56. Teepe R, Brumme R, Beese F (2000) Nitrous oxide emissions from frozen soils under agricultural, fallow and forest land. Soil Biology and Biochemistry 32:1807–1810CrossRefGoogle Scholar
  57. Ussiri D, Lal R (2013) Soil emission of nitrous oxide and its mitigation. Springer, Netherlands, pp 63–96Google Scholar
  58. Vermue A, Philippot L, Munier-Jolain N, Hénault C, Nicolardot B (2013) Influence of integrated weed management system on N-cycling microbial communities and N2O emissions. Plant and Soil 373:501–514CrossRefGoogle Scholar
  59. Walker JT, Gero CD, Vose JM, Swank WT (2002) Nitrogen trace gas emissions from a riparian ecosystem in sot&em Appalachia. Chemosphere 49:1389–1398CrossRefGoogle Scholar
  60. Wang L, Song C, Hu J, Yang T (2010) Response of regeneration diversity of Carex Lasiocarpa community to different water levels in Sanjiang Plain, China. Chinese Geographical Science 20:37–42CrossRefGoogle Scholar
  61. Wrage N, Velthof G, van Beusichem M, Oenema O (2001) Role of nitrifier denitrification in the production of nitrous oxide. Soil Biology and Biochemistry 33:1723–1732CrossRefGoogle Scholar
  62. Yan X, Shi S, Du L, Xing G (2000) Pathways of N2O emissions from rice paddy soil. Soil Biology and Biochemistry 32:437–440CrossRefGoogle Scholar
  63. Yang J, Liu J, Hu X, Li X, Wang Y, Li H (2013) Effect of water table level on CO2, CH4 and N2O emissions in a freshwater marsh of Northeast China. Soil Biology and Biochemistry 61:52–60CrossRefGoogle Scholar
  64. Yoshida T, Alexander M (1970) Nitrous oxide formation by Nitrosomonas europaea and heterotropic microorganisms. Soil Science Society of America Journal 34:880–882CrossRefGoogle Scholar
  65. Yu JB, Liu JS, DWang J, Sun WD, Patrick WH, Meixner FX (2007a) Nitrous oxide emission from Deyeuxia angustifolia freshwater marsh in Northeast China. Environmental Management 40:613–622CrossRefGoogle Scholar
  66. Yu, J. B., W. D. Sun, J. S. Liu, J. D. Wang, J. S. Yang and F. X. Meixner (2007b) Enhanced net formations of nitrous oxide and methane underneath the frozen soil in Sanjiang wetland, northeastern China. Journal of Geophysical Research 112:1–8. D07111Google Scholar
  67. Yu, K., G. Chen and N. S. Publishers (2009) Nitrous oxide emissions from terrestrial plants: observations, mechanisms and implications. In: Sheldon, A.I., Barnbart, E.P. (Eds.), Nitrous oxide emissions research Progress:85–104Google Scholar
  68. Zhang J, Song C, Yang W (2005) Cold season CH4, CO2 and N2O fluxes from freshwater marshes in Northeast China. Chemosphere 59:1703–1705CrossRefGoogle Scholar
  69. Zhang L, Song C, Zheng X, Wang D, Wang Y (2006) Effects of nitrogen on the ecosystem respiration, CH4 and N2O emissions to the atmosphere from the freshwater marshes in Northeast China. Environmental Geology 52:529–539CrossRefGoogle Scholar
  70. Zhang J, Müller C, Cai Z (2015) Heterotrophic nitrification of organic N and its contribution to nitrous oxide emissions in soils. Soil Biology and Biochemistry 84:199–209CrossRefGoogle Scholar
  71. Zimov S, Schuur E, Chapin F (2006) Permafrost and the global carbon budget. Science 312:1612–1613CrossRefGoogle Scholar

Copyright information

© Society of Wetland Scientists 2018

Authors and Affiliations

  • Liquan Song
    • 1
  • Yunlong Yao
    • 2
  • Weifeng Gao
    • 1
  • Tijiu Cai
    • 3
  • Qingbo Wang
    • 4
  • Dongfeng Fu
    • 4
  • Xiaoxin Sun
    • 3
  • Hong Liang
    • 5
    Email author
  • Dawen Gao
    • 1
    • 5
    • 6
    Email author
  1. 1.Center for Ecological ResearchNortheast Forestry UniversityHarbinChina
  2. 2.College of Wildlife ResourcesNortheast Forestry UniversityHarbinChina
  3. 3.College of ForestryNortheast Forestry UniversityHarbinChina
  4. 4.Heilongjiang Sanjiang National Nature Reserve AuthorityFuyuanChina
  5. 5.School of EnvironmentHarbin Institute of TechnologyHarbinChina
  6. 6.State Key Laboratory of Urban Water Resource and EnvironmentHarbin Institute of TechnologyHarbinChina

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