Skip to main content
Log in

Effect of litter nitrogen on decomposition and microbial biomass inSpartina alterniflora

  • Published:
Microbial Ecology Aims and scope Submit manuscript

Abstract

The effect on decomposition of 4 different levels of nitrogen in aerial tissue ofSpartina alterniflora, collected at the end of its growing season litter, was studied in laboratory percolators for 56 days at 20‡C. The CO2 evolution and the release of organic nitrogen and organic carbon were monitored. From these data, the ash-free dry weight (AFDW), nitrogen (N) content, and carbon∶nitrogen (C/N) ratio were calculated at various times during decomposition. Fungal biomass, bacterial biomass, and the relative autoradiographic activity of bacteria were measured at the end of the study. Decomposition was significantly affected by the nitrogen content of the litter. A 55% increase in plant N increased overall weight loss and k by 50% and 40%, respectively. Furthermore, k (calculated from time course weight loss data) responded linearly to the 4 different levels of nitrogen inSpartina tissue. Fungi appear to dominate the microbial community. At the end of the experiment, fungal biomass was between 2.23 and 3.08% of the AFDW, and was calculated to contain 12 to 22% of the nitrogen in the litter. Bacterial biomass was 1/10 of the fungal biomass, and 12–17% of the bacteria were active. The total microbial biomass was not affected by increased plant nitrogen. In the course of decomposition, the organic nitrogen and carbon were highest in the effluent water in all treatments during the first 8 days. The respiration rate (CO2 evolution) first increased to a maximum at day 18 and then decreased to a constant rate (1–2 mg C/day/g detritus). Respiration was highest in the high N litter. The C/N ratio in all treatments increased from the start to day 8, then decreased to day 20. In low N litter, C/N then increased again as a result of increased total organic nitrogen (TON) loss relative to carbon mineralization. In the high N, this was reversed.

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

Access this article

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

Instant access to the full article PDF.

Similar content being viewed by others

References

  1. Baath E, Lohm U, Lundgren B, Rösswall T, Söderström B, Sohlenius B, Wiren A (1978) The effect of nitrogen and carbon supply on the development of soil organism populations and pine seedlings: A microcosm experiment. Oikos 31:153–163

    Google Scholar 

  2. Baath E, Söderström B (1979) Fungal biomass and fungal immobilization of plant nutrients in Swedish coniferous forest soils. Rev Ecol Biol Sol 16:466–489

    Google Scholar 

  3. Baath E, Söderström B (1979) The significance of hyphal diameter in calculation of fungal biovolume. Oikos 33:11–14

    Google Scholar 

  4. Bell EA (1980) The non-protein amino acids of higher plants. Endeavour 4:102–107

    Google Scholar 

  5. Berg B, Söderström B (1979) Fungal biomass and nitrogen in decomposing Scots pine needle litter. Soil Biol Biochem 11:339–341

    Google Scholar 

  6. D'elia CE, Steudler PA, Corwin N (1977) Determination of total nitrogen in aqueous samples using persulfate digestion. Limnol Oceanogr 22:760–764

    Google Scholar 

  7. Ferguson RL, Rublee P (1976) Contribution of bacteria to standing crop of coastal plankton. Limnol Oceanogr 21:141–145

    Google Scholar 

  8. Frankland JC, Lindley DK, Swift MJ (1978) A comparison of two methods for the estimation of biomass in leaf litter. Soil Biol Biochem 10:323–333

    Google Scholar 

  9. Gosselink JG, Kirby CJ (1974) Decomposition of salt marsh grass,Spartina alterniflora Loisel. Limnol Oceanogr 19:825–832

    Google Scholar 

  10. Hobbie JE, Daley RJ, Jasper S (1977) Use of Nuclepore filters for counting bacteria by fluorescence microscopy. Appl Environ Microbiol 33:1225–1228

    PubMed  Google Scholar 

  11. Horne RA (1969) Marine Chemistry. Wiley-Interscience, New York, p 586

    Google Scholar 

  12. Howarth RW, Fisher SG (1976) Carbon, nitrogen, and phosphorus dynamics during leaf decay in nutrient-enriched stream microecosystems. Fresh Biol 6:221–228

    Google Scholar 

  13. Jones PCT, Mollison JE (1948) A technique for the quantitative estimation of soil microorganisms. J Gen Microbiol 2:54–69

    Google Scholar 

  14. Lee C, Howarth RW, Howes BL (1980) Sterols in decomposingSpartina alterniflora and the use of ergosterol in estimating the contribution of fungi to detrital nitrogen. Limnol Oceanogr 25:290–303

    Google Scholar 

  15. Lee JJ (1980) A conceptual model of marine detrital decomposition and the organisms associated with the process. In: Droop MR, Jannasch HW (eds), Advances in aquatic microbiology 2 pp 257–291

  16. Marinucci AC (1982) Trophic importance ofSpartina alterniflora production and decomposition to the marsh-estuarine ecosystem. Biol Conserv 22:35–58

    Google Scholar 

  17. Marinucci AC (1982) Carbon and nitrogen fluxes during decomposition ofSpartina alterniflora in a flow-through percolator. Biol Bull 162:53–69

    Google Scholar 

  18. Marinucci AC, Bartha R (1982) Biomagnification of Aroclor 1242 in decomposingSpartina litter. Appl Environ Microbial 44:669–677

    Google Scholar 

  19. Marinucci AC, Bartha R (1982) A component model of decomposition ofSpartina alterniflora in a New Jersey salt marsh. Can J Bot 60:1618–1624

    Google Scholar 

  20. Melillo JM, Aber JD, Muratore JF (1982) The influence of substrate quality on leaf litter decay in a northern hardwood forest. Ecology 63:621–626

    Google Scholar 

  21. Menzel DW, Vaccaro RF (1964) The measurement of dissolved organic and particulate carbon in seawater. Limnol Oceanogr 9:138–142

    Google Scholar 

  22. Meyer-Reil L-A (1978) Autoradiography and epifluorescence microscopy combined for the determination of number and spectrum of actively metabolizing bacteria in natural waters. Appl Environ Microbiol 36:506–512

    PubMed  Google Scholar 

  23. Newell SY (1981) Fungi and bacteria in or on leaves of eelgrass (Zostera marina L.) from Chesapeake Bay. Appl Environ Microbiol 41:1219–1224

    Google Scholar 

  24. Newell SY, Hicks RE (1982) Direct-count estimates of fungal and bacterial biovolume in dead leaves of smooth cordgrass (Spartina alterniflora Loisel). Estuaries 5:246–260

    Google Scholar 

  25. Olsen FCW (1950) Quantitative estimates of filamentous algae. Trans Amer Microsc Soc 69: 272–270

    Google Scholar 

  26. Parnas H (1975) Model for decomposition of organic materials by microorganisms. Soil Biol Biochem 7:161–169

    Google Scholar 

  27. Ross DJ, Tate KR, Cairns A, Pansier EA (1980) Microbial biomass estimations in soils from tussock grasslands by three biochemical procedures. Soil Biol Biochem 12:375–381

    Google Scholar 

  28. Sharp JH (1973) Total organic carbon in seawater. Comparison of measurements using persulfate oxidation and high temperature combustion. Mar Chem 1:211–229

    Google Scholar 

  29. StÄÄf H (1980) Influence of chemical composition, addition of raspberry leaves, and nitrogen supply on decomposition rate and dynamics of nitrogen and phosphorus in beech leaf litter. Oikos 35:55–62

    Google Scholar 

  30. Swift MJ, Heal OW, Anderson JM (1979) Decomposition in terrestrial ecosystems. Studies in ecology Vol 5. University of California Press, Los Angeles, p 372

    Google Scholar 

  31. Valiela I, Teal JM, Sass W (1975) Production and dynamics of salt marsh vegetation and the effects of experimental treatment with sewage sludge: Biomass, production, and species composition. J Appl Ecol 12:973–982

    Google Scholar 

  32. van Veen JA, Paul EA (1979) Conversion of biovolume measurements of soil organisms, grown under various moisture tensions, to biomass and their nutrient content. Appl Environ Microbiol 37:686–692

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Marinucci, A.C., Hobbie, J.E. & Helfrich, J.V.K. Effect of litter nitrogen on decomposition and microbial biomass inSpartina alterniflora . Microb Ecol 9, 27–40 (1983). https://doi.org/10.1007/BF02011578

Download citation

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF02011578

Keywords

Navigation