Skip to main content

Advertisement

Log in

Response of N2O emissions to elevated water depth regulation: comparison of rhizosphere versus non-rhizosphere of Phragmites australis in a field-scale study

  • Research Article
  • Published:
Environmental Science and Pollution Research Aims and scope Submit manuscript

Abstract

Emissions of nitrous oxide (N2O) from wetland ecosystems are globally significant and have recently received increased attention. However, relatively few direct studies of these emissions in response to water depth-related changes in sediment ecosystems have been conducted, despite the likely role they play as hotspots of N2O production. We investigated depth-related differential responses of the dissolved inorganic nitrogen distribution in Phragmites australis (Cav.) Trin. ex Steud. rhizosphere versus non-rhizosphere sediments to determine if they accelerated N2O emissions and the release of inorganic nitrogen. Changes in static water depth and P. australis growth both had the potential to disrupt the distribution of porewater dissolved NH4 +, NO3 , and NO2 in profiles, and NO3 had strong surface aggregation tendency and decreased significantly with depth. Conversely, the highest NO2 contents were observed in deep water and the lowest in shallow water in the P. australis rhizosphere. When compared with NO3 , NH4 +, and NO2 , fluxes from the rhizosphere were more sensitive to the effects of water depth, and both fluxes increased significantly at a depth of more than 1 m. Similarly, N2O emissions were obviously accelerated with increasing depth, although those from the rhizosphere were more readily controlled by P. australis. Pearson’s correlation analysis showed that water depth was significantly related to N2O emission and NO2 fluxes, and N2O emissions were also strongly dependent on NO2 fluxes (r = 0.491, p < 0.05). The results presented herein provide new insights into inorganic nitrogen biogeochemical cycles in freshwater sediment ecosystems.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Subscribe and save

Springer+
from $39.99 /Month
  • Starting from 10 chapters or articles per month
  • Access and download chapters and articles from more than 300k books and 2,500 journals
  • Cancel anytime
View plans

Buy Now

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1
Fig. 2
Fig. 3
Fig. 4
Fig. 5

Similar content being viewed by others

Explore related subjects

Discover the latest articles and news from researchers in related subjects, suggested using machine learning.

References

  • Bange HW, Rapsomanikis S, Andreae MO (1996) Nitrous oxide in coastal waters. Glob Biogeochem Cycles 10:197–207

    Article  CAS  Google Scholar 

  • Casanova MT, Brock MA (2000) How do depth, duration and frequency of flooding influence the establishment of wetland plant communities? Plant Ecol 147:237–250

    Article  Google Scholar 

  • Christensen PB, Nielsen LP, Revsbech NP, Sbrensen J (1989) Microzonation of denitrification activity in stream sediments as studied with a combined oxygen and nitrous oxide microsensor. Appl Environ Microbial 55:1234–1241

    CAS  Google Scholar 

  • Clevering OA, Hundschneid MPJ (1998) Plastic and non-plastic variation in growth of newly established clones of Scirpus (Bolboschoenus) maritimus L. grown at different water depths. Aquat Bot 62:1–17

    Article  Google Scholar 

  • Coops H, van den Brink FWB, van der Velde G (1996) Growth and morphological responses of four helophyte species in an experimental water-depth gradient. Aquat Bot 54:11–24

    Article  Google Scholar 

  • Elberling B, Christiansen HH, Hansen BU (2010) High nitrous oxide production from thawing permafrost. Nat Geosci 3:332–355

    Article  CAS  Google Scholar 

  • Froend RH, McComb AJ (1994) Distribution, productivity and reproductive phenology of emergent macrophytes in relation to water regimes at wetlands of south-western Australia. Aust J Mar Freshwater Res 45:1491–1508

    Article  Google Scholar 

  • Grace JB (1989) Effects of water depth on Typha latifolia and Typha domingensis. Am J Bot 76:762–768

    Article  Google Scholar 

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

    Article  CAS  Google Scholar 

  • Johnson-Beebout SE, Angeles OR, Alberto MCR, Buresh RJ (2009) Simultaneous minimization of nitrous oxide and methane emission from rice paddy soils is improbable due to redox potential changes with depth in a greenhouse experiment without plants. Geoderma 149:45–53

    Article  CAS  Google Scholar 

  • Kohl J-G, Henze R, Kühl H (1996) Evaluation of the ventilation resistance to convective gas-flow in the rhizomes of natural reed-beds of Phragmites australis (Cav.) Trin ex Steud. Aquat Bot 54:199–210

    Article  Google Scholar 

  • Kristensen E (2000) Organic matter diagenesis at the oxic/anoxic interface in coastal marine sediments, emphasis on the role of burrowing animals. Hydrobiologia 426:1–24

    Article  CAS  Google Scholar 

  • Kroeze C, Seitzinger SP (1998) Nitrogen inputs to rivers, estuaries and continental shelves and related nitrous oxide emissions in 1990 and 2050: a global model. Nutr Cycl Agroecosyst 52:195–212

    Article  CAS  Google Scholar 

  • Laursen AE, Seitzinger SP (2002) The role of denitrification in nitrogen removal and carbon mineralization in Mid-Atlantic Bight sediments. Cont Shelf Res 22:1397–1416

    Article  Google Scholar 

  • Lawson SE, McGlathery KJ, Wiberg PL (2012) Enhancement of sediment suspension and nutrient flux by benthic macrophytes at low biomass. Mar Ecol Prog Ser 448:259–270

    Article  Google Scholar 

  • Lerman A (1988) Geochemical processes, water and sediment environment. Robert E. Krieger Publishing, Malabar, FL

    Google Scholar 

  • Liu Y, Zhang JX, Zhang XL, Xie SG (2014) Depth-related changes of sediment ammonia-oxidizing microorganisms in a high-altitude freshwater wetland. Appl Microbiol Biotechnol 98:5697–5707

    Article  CAS  Google Scholar 

  • Maurer DA, Zedler JB (2002) Differential invasion of a wetland grass explained by tests of nutrients and light availability on establishment and clonal growth. Oecologia 131:279–288

    Article  Google Scholar 

  • McGlathery KJ, Sundbäck K, Anderson IC (2007) Eutrophication in shallow coastal bays and lagoons: the role of plants in the coastal filter. Mar Ecol Prog Ser 348:1–18

    Article  CAS  Google Scholar 

  • Miao SL, Sklar FH (1998) Biomass and nutrient allocation of sawgrass and cattail along a nutrient gradient in the Florida Everglades. Wetl Ecol Manage 5:245–263

    Article  Google Scholar 

  • Murray LG, Mudge SM, Newton A, Icely JD (2006) The effect of benthic sediments on dissolved nutrient concentrations and fluxes. Biogeochemistry 81:159–178

    Article  CAS  Google Scholar 

  • Nielsen LP, Christensen PB, Revsbech NP, S¢ensen J (1990) Denitrification and photosynthesis in stream sediment studied with microsensor and whole-core techniques. Limnol Oceanogr 35(5):1135–l144

    Article  CAS  Google Scholar 

  • Nielsen OI, Gribsholt B, Kristensen E, Revsbech NP (2004) Microscale distribution of oxygen and nitrate in sediment inhabited by Nereis diversicolor: spatial patterns and estimated reaction rates. Aquat Microb Ecol 34(1):23–32

    Article  Google Scholar 

  • Øvreås L (2000) Population and community level approaches for analyzing microbial diversity in natural environments. Ecol Lett 3:236–251

    Article  Google Scholar 

  • Peter RT, Graeme E, Batley Simon CA (1995) Pore water sampling with sediment peepers. Trends Anal Chem 14(6):250–256

    Article  Google Scholar 

  • Rasheed M, Badran MI, Huettel M (2003) Influence of sediment permeability and mineral composition on organic matter degradation in three sediments from the Gulf of Aqaba, Red Sea. Estuar Coast Shelf Sci 57:369–384

    Article  CAS  Google Scholar 

  • Seitzinger SP, Kroeze C (1998) Global distribution of nitrous oxide production and N inputs in freshwater and coastal marine ecosystems. Glob Biogeochem Cycles 12(1):93–113

    Article  CAS  Google Scholar 

  • Skinner T, Adams JB, Gama PT (2006) The effect of mouth opening on the bio-mass and community structure of microphytobenthos in a small oligotrophic estuary. Estuar Coast Shelf Sci 70:161–168

    Article  Google Scholar 

  • Song JM (1997) Sediments-water interface chemistry in the nearshore of China. Ocean Press, Beijing, China, pp 6–8

    Google Scholar 

  • Sorrell BK, Tanner CC (2000) Convective gas flow and internal aeration in Eleocharis sphacelata in relation to water depth. J Ecol 88:778–789

    Article  Google Scholar 

  • Sorrell BK, Tanner CC, Sukias JPS (2002) Effects of water depth and substrate on growth and morphology of Eleocharis sphacelata: implications for culm support and internal gas transport. Aquat Bot 73:93–106

    Article  Google Scholar 

  • Strand JA, Weisner SEB (2001) Morphological plastic responses to water depth and wave exposure in an aquatic plant (Myriophyllum spicatum). J Ecol 89:166–175

    Article  Google Scholar 

  • Sundbäck K, Miles A, Goransson E (2000) Nitrogen fluxes, denitrification and the role of microphytobenthos in microtidal shallow-water sediments: an annual study. Mar Ecol Prog Ser 200:59–76

    Article  Google Scholar 

  • Tanner CC, D’Eugenio J, McBride GB, Sukias JPS, Thompson K (1999) Effect of water level fluctuation on nitrogen removal from constructed wetland mesocosms. Ecol Eng 12:67–92

    Article  Google Scholar 

  • Thomaz SM, Chambers PA, Pierini SA, Pereira G (2007) Effects of phosphorus and nitrogen amendments on the growth of Egeria najas. Aquat Bot 86:191–196

    Article  CAS  Google Scholar 

  • Wang H, He ZL, Lu ZM, Zhou JZ, Van Nostrand DJ, Xu XH, Zhang ZJ (2012) Genetic linkage of soil carbon pools and microbial functions in subtropical freshwater wetlands in response to experimental warming. Appl Environ Microbiol 78:7652–7661

    Article  CAS  Google Scholar 

  • Weisner SEB, Strand JA (1996) Rhizome architecture in Phragmites australis in relation to water depth: implications for within-plant oxygen transport distances. Folia geobot phytotax 31:91–97

    Article  Google Scholar 

  • White SD, Ganf GG (2002) A comparison of the morphology, gas space anatomy and potential for internal aeration in Phragmites australis under variable and static water regimes. Aquat Bot 73:115–127

    Article  Google Scholar 

  • Xie Y, An S, Wu B (2005) Resource allocation in the submerged plant Vallisneria natans related to sediment type, rather than water column nutrients. Freshwater Bio 50:391–402

    Article  Google Scholar 

Download references

Acknowledgements

Support for the present study was provided by the National Natural Science Foundation of China (Nos. 41203064 and 41203065), the Natural Science Foundation of Jiangsu Province, China (Nos. BK20131464 and BK20131465), and the National Special Water Project Chaohu Program of China (No. 2012ZX07103-002).

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Xiao-zhi Gu.

Additional information

Responsible editor: Philippe Garrigues

Rights and permissions

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Gu, Xz., Chen, Kn. & Wang, Zd. Response of N2O emissions to elevated water depth regulation: comparison of rhizosphere versus non-rhizosphere of Phragmites australis in a field-scale study. Environ Sci Pollut Res 23, 5268–5276 (2016). https://doi.org/10.1007/s11356-015-5776-9

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s11356-015-5776-9

Keywords