Decomposition of Scots pine fine woody debris in boreal conditions: Implications for estimating carbon pools and fluxes

Abstract Litter quality and environmental effects on Scots pine ( Pinus sylvestris L.) fine woody debris (FWD) decomposition were examined in three forestry-drained peatlands representing different site types along a climatic gradient from the north boreal (Northern Finland) to south (Southern Finland) and hemiboreal (Central Estonia) conditions. Decomposition (percent mass loss) of FWD with diameter ≤10 mm (twigs) and FWD with diameter >10 mm (branches) was measured using the litter bag method over 1–4-year periods. Overall, decomposition rates increased from north to south, the rate constants ( k values) varying from 0.128 to 0.188 year −1 and from 0.066 to 0.127 year −1 for twigs and branches, respectively. On average, twigs had lost 34%, 19% and 19%, and branches 25%, 17% and 11% of their initial mass after 2 years of decomposition at the hemiboreal, south boreal and north boreal sites, respectively. After 4 years at the south boreal site the values were 48% for twigs and 42% for branches. Based on earlier studies, we suggest that the decomposition rates that we determined may be used for estimating Scots pine FWD decomposition in the boreal zone, also in upland forests. Explanatory models accounted for 50.4% and 71.2% of the total variation in FWD decomposition rates when the first two and all years were considered, respectively. The variables most related to FWD decomposition included the initial ash, water extractives and Klason lignin content of litter, and cumulative site precipitation minus potential evapotranspiration. Simulations of inputs and decomposition of Scots pine FWD and needle litter in south boreal conditions over a 60-year period showed that 72 g m −2 of organic matter from FWD vs. 365 g m −2 from needles accumulated in the forest floor. The annual inputs varied from 5.7 to 15.6 g m −2 and from 92 to 152 g m −2 for FWD and needles, respectively. Each thinning caused an increase in FWD inputs, up to 510 g m −2 , while the needle inputs did not change dramatically. Because the annual FWD inputs were lowered following the thinnings, the overall effect of thinnings on C accumulation from FWD was slightly negative. The contribution of FWD to soil C accumulation, relative to needle litter, seems to be rather minor in boreal Scots pine forests.

[1]  C. Westman,et al.  Nutrient dynamics of drained peatland forests , 2003 .

[2]  John Pastor,et al.  Decomposition of aspen, spruce, and pine boles on two sites in Minnesota , 1993 .

[3]  P. Groffman,et al.  Snow depth manipulation and its influence on soil frost and water dynamics in a northern hardwood forest , 2001 .

[4]  A. Gallardo,et al.  Changes in chemical composition of Pinus sylvestris needle litter during decomposition along a European coniferous forest climatic transect. , 2003 .

[5]  C. Preston,et al.  Variability in litter quality and its relationship to litter decay in Canadian forests. , 2000 .

[6]  M. Starr,et al.  Decomposition and nutrient release from logging residues after clear-cutting of mixed boreal forest , 2004, Plant and Soil.

[7]  H. Mäkinen,et al.  Predicting wood and tracheid properties of Norway spruce , 2007 .

[8]  M. G. Ryan,et al.  A comparison of methods for determining proximate carbon fractions of forest litter , 1990 .

[9]  Hannu Hökkä,et al.  Height-diameter curves with random intercepts and slopes for trees growing on drained peatlands , 1997 .

[10]  N. Shurpali,et al.  Heterotrophic soil respiration in forestry-drained peatlands , 2007 .

[11]  A. Mäkelä,et al.  Potential litterfall of Scots pine branches in southern Finland , 2004 .

[12]  M. Harmon,et al.  Effects of temperature and moisture on carbon respired from decomposing woody roots , 2000 .

[13]  Björn Berg,et al.  Effect of N deposition on decomposition of plant litter and soil organic matter in forest systems , 1997 .

[14]  M. Hunter,et al.  Phenotypic variation in oak litter influences short- and long-term nutrient cycling through litter chemistry , 2005 .

[15]  V. Meentemeyer,et al.  Litter mass loss rates in pine forests of Europe and Eastern United States: some relationships with climate and litter quality , 1993 .

[16]  L. Boddy Carbon dioxide release from decomposing wood: Effect of water content and temperature , 1983 .

[17]  Björn Berg,et al.  Litter decomposition in a transect of Norway spruce forests: substrate quality and climate control , 2000 .

[18]  J. Fyles,et al.  Rates of litter decomposition over 6 years in Canadian forests: influence of litter quality and climate , 2002 .

[19]  S. Güsewell,et al.  Nutrient limitation and enzyme activities during litter decomposition of nine wetland species in relation to litter N : P ratios , 2005 .

[20]  T. Penttilä,et al.  Stand structural dynamics on drained peatlands dominated by Scots pine , 2005 .

[21]  L. Knudsen,et al.  The use of the angular transformation in biological assays. , 1947, Journal of the American Statistical Association.

[22]  W. Kutsch,et al.  Leaf litter nitrogen concentration as related to climatic factors in Eurasian forests , 2006 .

[23]  B. Berg Initial rates and limit values for decomposition of Scots pine and Norway spruce needle litter : a synthesis for N-fertilized forest stands , 2000 .

[24]  J. B. Kenworthy,et al.  Chemical Analysis of Ecological Materials. , 1976 .

[25]  P. Martikainen,et al.  Change in fluxes of carbon dioxide, methane and nitrous oxide due to forest drainage of mire sites of different trophy , 2004, Plant and Soil.

[26]  W. Parton,et al.  Long‐term dynamics of pine and hardwood litter in contrasting environments: toward a global model of decomposition , 2000 .

[27]  R. Aerts,et al.  Does initial litter chemistry explain litter mixture effects on decomposition? , 2003, Oecologia.

[28]  J. Laine,et al.  Vuosina 1930-1978 metsäojitetut suot: ojitusalueiden inventoinnin tuloksia. , 1986 .

[29]  B. Berg,et al.  Litter decomposition rate is dependent on litter Mn concentrations , 2007 .

[30]  P. Bottner,et al.  Litter decomposition, climate and liter quality. , 1995, Trends in ecology & evolution.

[31]  H. Goldstein Multilevel Statistical Models , 2006 .

[32]  D. Moorhead,et al.  Climate and litter quality controls on decomposition: An analysis of modeling approaches , 1999 .

[33]  M. Coûteaux,et al.  A climate response function explaining most of the variation of the forest floor needle mass and the needle decomposition in pine forests across Europe , 2006, Plant and Soil.

[34]  Steve Frolking,et al.  Plant biomass and production and CO2 exchange in an ombrotrophic bog , 2002 .

[35]  T. Penttilä,et al.  Individual-tree basal area growth models for Scots pine, pubescent birch and Norway spruce on drained peatlands in Finland. , 1997 .

[36]  R. Edmonds Decomposition rates and nutrient dynamics in small-diameter woody litter in four forest ecosystems in Washington, U.S.A. , 1987 .

[37]  A. Grimvall,et al.  Humic Substances in the Aquatic and Terrestrial Environment , 1991 .

[38]  M. Johansson Decomposition rates of Scots pine needle litter related to site properties, litter quality, and climate , 1994 .

[39]  V. Meentemeyer,et al.  Litter quality in a north European transect versus carbon storage potential , 2002, Plant and Soil.

[40]  H. Henttonen,et al.  Estimation of local values of monthly mean temperature, effective temperature sum and precipitation sum from the measurements made by the Finnish Meteorological Office , 1983 .

[41]  R. Aerts,et al.  Nutritional and plant-mediated controls on leaf litter decomposition of Carex species , 1997 .

[42]  Ulrich Müller,et al.  Genetic parameters of growth and wood quality traits in Picea abies , 2004 .

[43]  Raija Laiho,et al.  The contribution of coarse woody debris to carbon, nitrogen, and phosphorus cycles in three Rocky Mountain coniferous forests , 1999 .

[44]  D. Coleman,et al.  Soil microarthropod contributions to decomposition dynamics : Tropical-temperate comparisons of a single substrate , 1999 .

[45]  Risto Ojansuu,et al.  Kuukauden keskilämpötilan, lämpösumman ja sademäärän paikallisten arvojen johtaminen Ilmatieteen laitoksen mittaustiedoista. , 1983 .

[46]  J. Liski,et al.  Litter decomposition affected by climate and litter quality—Testing the Yasso model with litterbag data from the Canadian intersite decomposition experiment , 2005 .

[47]  S. K. Schmidt,et al.  Microbial growth under the snow: Implications for nutrient and allelochemical availability in temperate soils , 2004, Plant and Soil.

[48]  M. Hunter,et al.  PHENOTYPIC DIVERSITY INFLUENCES ECOSYSTEM FUNCTIONING IN AN OAK SANDHILLS COMMUNITY , 2002 .

[49]  Timo Penttilä,et al.  Dynamics of plant‐mediated organic matter and nutrient cycling following water‐level drawdown in boreal peatlands , 2003 .

[50]  Anssi Ahtikoski,et al.  Applying the MOTTI simulator to analyse the effects of alternative management schedules on timber and non-timber production , 2005 .

[51]  B. R. Taylor,et al.  Nitrogen and Lignin Content as Predictors of Litter Decay Rates: A Microcosm Test , 1989 .

[52]  V. Meentemeyer,et al.  Macroclimate and Lignin Control of Litter Decomposition Rates , 1978 .

[53]  C. W. Thornthwaite An Approach Toward a Rational Classification of Climate , 1948 .

[54]  Bengt A. Olsson,et al.  Decomposition and nutrient release from Picea abies (L.) Karst. and Pinus sylvestris L. logging residues , 2000 .

[55]  E. Bringmark,et al.  Large-scale pattern of mor layer degradability in Sweden measured as standardized respiration , 1991 .

[56]  M. Johansson,et al.  Influence of mechanical site preparation on decomposition and nutrient dynamics of Norway spruce (Picea abies (L.) Karst.) needle litter and slash needles , 1997 .

[57]  L. Condron,et al.  Decomposition and nutrient release from radiata pine (Pinus radiata) coarse woody debris , 2004 .

[58]  P. Bottner,et al.  Long-term effects of temperature on carbon mineralisation processes , 2001 .

[59]  J. Coulson,et al.  AN INVESTIGATION OF THE BIOTIC FACTORS DETERMINING THE RATES OF PLANT DECOMPOSITION ON BLANKET BOG , 1978 .

[60]  R. Wieder,et al.  Quantitative determination of organic fractions in highly organic, Sphagnum peat soils , 1998 .

[61]  R. Aerts,et al.  Initial litter respiration as indicator for long-term leaf litter decomposition of Carex species , 1997 .

[62]  C. Trettin,et al.  Scots pine litter decomposition along drainage succession and soil nutrient gradients in peatland forests, and the effects of inter-annual weather variation , 2004 .

[63]  J. Liski,et al.  Carbon and decomposition model Yasso for forest soils , 2005 .

[64]  H. Vasander,et al.  Changes in mesofauna abundance in peat soils drained for forestry , 2000 .

[65]  J. Olson,et al.  Energy Storage and the Balance of Producers and Decomposers in Ecological Systems , 1963 .

[66]  S. Frolking,et al.  EU peatlands: Current carbon stocks and trace gas fluxes , 2004 .

[67]  Mark E. Harmon,et al.  Nutrient stores and dynamics of woody detritus in a boreal forest: modeling potential implications at the stand level , 1999 .

[68]  Björn Berg,et al.  Plant Litter: Decomposition, Humus Formation, Carbon Sequestration , 2003 .

[69]  Björn Berg,et al.  Changes in organic chemical components of needle litter during decomposition. Long-term decomposition in a Scots pine forest. I , 1982 .

[70]  Hannu Hökkä,et al.  Modeling Mortality of Individual Trees in Drained Peatland Sites in Finland , 2003 .

[71]  John F. Muratore,et al.  Nitrogen and Lignin Control of Hardwood Leaf Litter Decomposition Dynamics , 1982 .

[72]  Björn Berg,et al.  Litter decomposition and organic matter turnover in northern forest soils , 2000 .

[73]  B. R. Taylor,et al.  Substrate control of litter decomposition in four Rocky Mountain coniferous forests , 1991 .

[74]  C. Prescott Do rates of litter decomposition tell us anything we really need to know , 2005 .

[75]  T. Moore Winter-Time Litter Decomposition in A Subarctic Woodland , 1983, Arctic and Alpine Research.