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Impact of NH4NO3 on microbial biomass C and N and extractable DOM in raised bog peat beneath Sphagnum capillifolium and S. recurvum

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Abstract

Regular bi-weekly additions of NH4NO3, equivalent to a rate of 3 g N m−2 yr−1, were applied to cores of Sphagnum capillifolium, inhabiting hummocks and S. recurvum a pool and hollow colonizer, in a raisedbog in north east Scotland. Microbial biomass C and N,both measured by chloroform extraction, showed similarseasonal patterns and, for most depths, the effects ofadded N on microbial biomass C and N changed withtime. The addition of inorganic N had greatest effectduring October when the water table had risen to thesurface and microbial C and N in the untreated coreshad decreased. Microbial C and N were maintained at75 g C m−2 and 8.3 g N m−2 above the values in the untreated cores and far exceeded the amounts of N that had been added up to that date (1 g N m−2) as NH4NO3. This increased microbial biomass was interpreted as leaching of carbonaceous material from the NH4NO3 treated moss resulting in greater resistance of the microbialbiomass to changes induced by the rising water table.Treatment with N also caused significant reductions inextractable dissolved organic N (DON) at 10–15 cmdepth, beneath the surface of the moss, but at lowerdepths to 25 cm no changes were observed. Extracteddissolved organic carbon (DOC) was not affected by Ntreatment and showed less seasonal variation than DON,such that the C:N ratio of dissolved organic matter(DOM) in all depths increased from approximately 4 inJuly to around 30 in December.

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References

  • Aerts R, Wallén B & Malmer N (1992) Growth-limiting nutrients in Sphagnum-dominated bogs subject to low and high atmospheric nitrogen supply. J. Ecol. 80: 131–140

    Google Scholar 

  • Anderson JPE & Domsch KH (1978) A physiological method for the quantitative measurement of microbial biomass in soil. Soil Biol. Biochem. 10: 215–221

    Google Scholar 

  • Baxter R, Emes MJ & Lee JA (1992) Effects of an experimentally applied increase in ammonium on growth and amino-acid metabolism of Sphagnum cuspidatum Ehrh. ex. Hoffm. from differently polluted areas. New Phytol. 120: 265–274

    Google Scholar 

  • Bremner JM (1965) Inorganic forms of nitrogen. In: Black CA (Ed) Methods of Soil Analysis, Part 2. (pp 1179–1206). American Society of Agronomy, Madison, Wisconsin, U.S.A.

    Google Scholar 

  • Brookes PC, Landman A, Pruden G & Jenkinson D S (1985) Chloroform fumigation and the release of soil nitrogen: a rapid direct extraction method to measure microbial biomass nitrogen in soil. Soil Biol. Biochem. 17: 837–842

    Google Scholar 

  • Chapman SB (1971) A simple conductimetric respirometer for field use. Oikos 22: 348–353

    Google Scholar 

  • ChengW & Virginia RA (1993) Measurement of microbial biomass in arctic tundra soils using fumigation-extraction and substrate-induced respiration procedures. Soil Biol. Biochem. 25: 135–141.

    Google Scholar 

  • Clymo RS & Reddaway, EJF (1974) Growth rate of Sphagnum rubellum Wils. on Pennine blanket bog. J. Ecol. 62: 191–196

    Google Scholar 

  • Crooke WM & SimpsonWE (1971) Determination of ammonium in Kjeldahl digests of crops by an automated procedure. J. Sci. Food Agric. 22: 9–10

    Google Scholar 

  • Damman AWH (1988) Regulation of nitrogen removal and retention in Sphagnum bogs and other peatlands. Oikos 51: 91–305

    Google Scholar 

  • Daniels RE & Eddy A (1985) Handbook of European Sphagna. Institute of Terrestrial Ecology, Natural Environment Research Council. Cambrian News, Aberystwyth, U.K.

    Google Scholar 

  • Genstat 5 Committee (1993) Genstat 5 Release 3 Reference Manual. Oxford University Press, Oxford Henriksen A & Selmer-Olsen AR (1970) Automatic methods for determining nitrate and nitrite in water and soil extracts. Analyst 95: 514–518

    Google Scholar 

  • INDITE (1994) Impacts of Nitrogen Deposition in Terrestrial Ecosystems. Report of the United Kingdom Review Group on Impacts of Atmospheric Nitrogen. Department of the Environment, London

    Google Scholar 

  • Kenward MG (1987) A method of comparing profiles of repeated measurements. Appl. Stats 36: 296–308

    Google Scholar 

  • Li YH and Vitt DH (1997) Patterns of retention and utilisation of aerially deposited nitrogen in boreal peatlands. Ecosci. 4: 106–116

    Google Scholar 

  • Nasholm T, Ekblad A, Nordin A, Giesler R, Hogberg H & Hogberg P (1998) Boreal forest plants take up organic nitrogen. Nature 392: 914–916

    Google Scholar 

  • Silcock DJ & Williams BL (1995) The fate and effects of inorganic nitrogen inputs to raised bog vegetation. In: Jenkins A, Ferrier RC & Kirby C (Eds) Ecosystem Manipulation Experiments. Ecosystems Research Report 20 (pp 44–48).

  • European Commission, Brussels Simola LK (1975) The effect of several protein amino acids and some inorganic nitrogen sources on the growth of Sphagnum nemorum. Physiol. Plant.35: 194–199

    Google Scholar 

  • Smolander A, Kurka A, Kitunen V & Mälkönen E (1994) Microbial biomass C and N, and respiratory activity in soil of repeatedly limed and N-and P-fertilized Norway spruce stands. Soil Biol. Biochem. 26: 957–962

    Google Scholar 

  • Sparling GP, Feltham CW, Reynolds J, West AW & Singleton P (1990) Estimation of soil microbial C by a fumigation-extraction method: use on soils of high organic matter content, and a reassessment of the kEC-factor. Soil Biol. Biochem. 22: 301–307

    Google Scholar 

  • von Post L (1929) Sveriges Geologiska Undersøknings torvinventering och nogra av dess hittils vunna resultat. Svenska Mosskulturfø.Tids. 36: 1–27

    Google Scholar 

  • Wardle DA (1998) Controls of temporal variability of the soil microbial biomass: a globalscale synthesis. Soil Biol. Biochem. 30: 1627–1637

    Google Scholar 

  • Williams BL, Shand CA, Hill M, O'Hara C, Smith S & Young ME (1995) A procedure for the simultaneous oxidation of total soluble nitrogen and phosphorus in extracts of fresh and fumigated soils and litters. Commun. Soil Sci. Plant Anal. 26: 91–106

    Google Scholar 

  • Williams BL & Silcock DJ (1997) Nutrient and microbial changes in the peat profile beneath Sphagnum magellanicum in response to additions of ammonium nitrate. J. Appl. Ecol. 34: 961–970

    Google Scholar 

  • Williams BL, Silcock DJ & Young MY (1999) Seasonal dynamics of N in two Sphagnum moss species and the underlying peat treated with 15NH4 15NO3. Biogeochem. 45: 285–302

    Google Scholar 

  • Williams BL & Sparling GP (1984) Extractable nitrogen and phosphorus in relation to microbial biomass in acid organic soils. Plant and Soil 76: 139–148

    Google Scholar 

  • Williams BL & Wheatley RE (1989) Nitrogen transformations in poorly-drained reseeded blanket peat under different management systems. Int. Peat J. 3: 97–106

    Google Scholar 

  • Woodin SJ & Lee JA (1987) The fate of some components of acidic deposition in ombrotrophic mires. Environ. Pollut. 45: 61–72

    Google Scholar 

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Williams, B.L., Silcock, D.J. Impact of NH4NO3 on microbial biomass C and N and extractable DOM in raised bog peat beneath Sphagnum capillifolium and S. recurvum . Biogeochemistry 49, 259–276 (2000). https://doi.org/10.1023/A:1006329707536

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