Temperature dependence of carbon mineralization and nitrous oxide emission in a temperate forest ecosystem

Ali Bagherzadeh , Rainer Brumme , Friedrich Beese

Journal of Forestry Research ›› 2008, Vol. 19 ›› Issue (2) : 107 -112.

PDF
Journal of Forestry Research ›› 2008, Vol. 19 ›› Issue (2) : 107 -112. DOI: 10.1007/s11676-008-0018-3
Research Paper

Temperature dependence of carbon mineralization and nitrous oxide emission in a temperate forest ecosystem

Author information +
History +
PDF

Abstract

The measurement of CO2 and N2O efflux from forest soils is of great importance in evaluating the role of forests as sequestering agents of atmospheric CO2 and nitrogen. To quantify the effect of site on temperature dependence of net C-mineralization and N2O-N emissions, three adjacent forest floors under beech, Norway spruce and mixed species stands were investigated at Solling forest, Germany, by an incubation experiment for three months. The investigated net C-mineralization and N2O-N emissions from all forest floors exhibited an exponential increase with respect to temperature elevation. The temperature coefficient function (Q10 value), was fitted to flux rates to describe the temperature sensitivity of forest floors on temperature in the range of 1–20°C. Comparing the fitted curves for temperature sensitivity of the forest floors in relation to net carbon mineralization and nitrous oxide emission rates revealed a strong positive correlation across all sites. For the whole data set of all stands, a Q10 value of 1.73–2.10 for net C-mineralization and 2.81–3.58 for N2O-N emissions per measured unit was found to describe the temperature dependency of net C-mineralization and N2O-N efflux at experimental site. The absence of clear differences between beech and spruce in mono and mixed species cultures on temperature dependencies of net C-mineralization and N2O-N emission rates indicated that the flux rates were not affected by species-specific differences of litter quality.

Keywords

beech / spruce / net C-mineralization / nitrous oxide emission / temperature / temperature sensitivity index (Q10)

Cite this article

Download citation ▾
Ali Bagherzadeh, Rainer Brumme, Friedrich Beese. Temperature dependence of carbon mineralization and nitrous oxide emission in a temperate forest ecosystem. Journal of Forestry Research, 2008, 19(2): 107-112 DOI:10.1007/s11676-008-0018-3

登录浏览全文

4963

注册一个新账户 忘记密码

References

[1]

Anderson J.M. Responses of soils to climate change Advances in Ecological Research, 1992, 22: 163-210.

[2]

Boone R.D., Nadelhoffer K.J., Canary J.D. Roots exert a strong influence on the temperature sensitivity of soil respiration Nature, 1998, 396: 570-572.

[3]

Borken W., Xu Y.-j., Davidson E., Beese F. Site and temporal variation of soil respiration in European beech, Norway spruce, and Scot pine forests Global Change Biology, 2002, 8: 1205-1216.

[4]

Brumme R. Mechanisms of carbon and nutrient release and retention in beech forest gaps, III. Environmental regulation of soil respiration and nitrous oxide emissions along a microclimatic gradient Plant and Soil, 1995, 168–169: 593-600.

[5]

Brumme R., Beese F. Effects of liming and nitrogen fertilization on emissions of CO2 and N2O from a temperate forest J Geophys Res., 1992, 97: 12851-12858.

[6]

Brumme R., Borken W., Finke S. Hierarchical control on nitrous oxide emission in forest ecosystems Global Biogeochem Cycles, 1999, 13(4): 1137-1148.

[7]

Chen H., Harmon M.E., Griffiths R.P., Hicks W. Effects of temperature and moisture on carbon respires from decomposing woody roots Forest Ecol and manage, 2000, 138: 51-64.

[8]

Cicerone R.J. Changes in stratospheric ozone Science, 1987, 237: 35-42.

[9]

Davidson E., Belk E., Boone R. Soil water content and temperature as independent or confounded factors controlling soil respiration in a temperate mixed hardwood forest Global Change Biology, 1998, 4: 217-227.

[10]

Fang C., Moncrieff J.B. The dependence of soil CO2 efflux on temperature Soil Biol and Biochem, 2001, 33: 155-165.

[11]

Groffman P.M. Ecology in nitrification and denitrification in soil evaluated at scales relevant to atmospheric chemistry, in Microbial production and consumption of greenhouse gases: Methane, nitrogen oxide and halomethanes, 1991 Washington D.C: American Society of Microbiology 201-217.

[12]

Houghton R.A., Davidson E.A., Woodwell G.M. Missing sinks, feedback, and understanding the role of terrestrial ecosystems in the global carbon balance Global Biogeochemical Cycles, 1998, 12: 25-34.

[13]

Jenkinson D.S., adams D.E., Wild A. Model estimates of CO2 emissions from soil in response to global warming Nature, 1991, 351: 304-306.

[14]

Kaetterer T., Reichstein M., Andren O., Lomander A. Temperature dependence of organic matter decomposition: a critical review using literature data analysed with different models Biol Fert Soils, 1998, 27: 258-262.

[15]

Kirschbaum M.U.F. The temperature dependence of soil organic matter decomposition, and the effect of global warming on soil organic C storage Soil biol and Biochem, 1995, 27: 753-760.

[16]

Kirschbaum M.U.F. Will changes in soil organic carbon act as a positive or negative feedback on global warming? Biogeochemistry, 2000, 48: 21-51.

[17]

Lloyd J., Taylor J.A. On the temperature dependence of soil respiration Functional Ecology, 1994, 8: 315-323.

[18]

Loftfield N., Flessa H., Augustin J., Beese F. Automated gas chromatographic system for rapid analysis of the atmospheric trace gases methane, carbon dioxide, and nitrous oxide Journal of Environmental Quality, 1997, 26(2): 560-564.

[19]

Meesenburg H., Meiwes K.J., Bartens H. Veraenderungen der Elementvorrate im Boden von Buchen-und Fichtenokosystemen im Solling Ber Freiburger Forstl Forschung, 1999, 7: 109-114.

[20]

Naegele W., Conrad R. Influence of soil pH on the nitrate reducing microbial populations and their potential to reduce nitrate to NO and N2O FEMS Microbial, 1990, 74: 49-58.

[21]

Nodar R., Acea M.J., Carballas T. Microbial response to Ca(OH)2 treatment in a forest soil FEMS Microbial Ecol., 1992, 86: 213-219.

[22]

Papen H., Von Berg R., Hellmann B., Rennenberg H. The effect of experimental acid precipitation and liming on chemolithotrophic and heterotrophic nitrification in soils of the Hoeglwald Forstwiss Forsch, 1991, 39: 111-116.

[23]

Raich J.W., Schlesinger W.H. The global carbon dioxide flux in soil respiration and its relationship to vegetation and climate Tellus, 1992, 44: 81-99.

[24]

Ramanathan V., Cicerone R., Singh H. B., Kiehl J.T. Trace gas trends and their potential role in climate change Journal of Geophysical Research, 1985, 90: 5547-5566.

[25]

Reichstein M., Bednorz F., Broll G., Kaetterer T. Temperature dependence of carbon mineralization: conclusions from a long-term incubation of subalpine soil samples Soil Biol and Biochem, 2000, 32: 947-958.

[26]

Schimel D.S., braswell B.H., Holland E.A., McKeown R., Ojima D.S., Painter T.H., Parton W.J., Townsend A.R. Climatic, edaphic, and biotic controls over storage and turnover of carbon in soils Global Biogeochemical Cycles, 1994, 8: 279-293.

[27]

Schlesinger W.H., Andrews J.A. Soil respiration and the global carbon cycle Biogeochemistry, 2000, 48: 7-20.

[28]

Sitaula B.K., Bakken L.R. N2O release from spruce forest soil, and relation with nitrification, CH4 uptake, temperature, moisture and fertilization Soil Biol and Biochem, 1993, 25: 1415-1421.

[29]

Tiktak A., Bredemeier M., Van Heerden K. The Solling dataset: Site characteristics, monitoring data and deposition scenarios Ecological Modelling, 1995, 83: 17-34.

[30]

Weier K.L., Doran J.W., Power J.W., Walters D.T. Denitrification and the denitrogen/nitrous oxide ratio as affected by soil water, available carbon, and nitrate Soil Sci Soc Am J, 1993, 57: 66-72.

[31]

Winkler J.P., Cherry R.S., Sclesinger W.H. The Q10 relationship of microbial respiration in a temperate forest soil Soil Biol and Biochem, 1996, 28: 1067-1072.

AI Summary AI Mindmap
PDF

114

Accesses

0

Citation

Detail

Sections
Recommended

AI思维导图

/