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Carbon balance and allocation of assimilated CO2 in Scots pine, Norway spruce, and Silver birch seedlings determined with gas exchange measurements and 14C pulse labelling

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Abstract

Carbon dioxide is released from the soil to the atmosphere in heterotrophic respiration when the dead organic matter is used for substrates for soil micro-organisms and soil animals. Respiration of roots and mycorrhiza is another major source of carbon dioxide in soil CO2 efflux. The partitioning of these two fluxes is essential for understanding the carbon balance of forest ecosystems and for modelling the carbon cycle within these ecosystems. In this study, we determined the carbon balance of three common tree species in boreal forest zone, Scots pine, Norway spruce, and Silver birch with gas exchange measurements conducted in laboratory in controlled temperature and light conditions. We also studied the allocation pattern of assimilated carbon with 14C pulse labelling experiment. The photosynthetic light responses of the tree species were substantially different. The maximum photosynthetic capacity (P max) was 2.21 μg CO2 s−1 g−1 in Scots pine, 1.22 μg CO2 s−1 g−1 in Norway spruce and 3.01 μg CO2 s−1 g−1 in Silver birch seedlings. According to the pulse labelling experiments, 43–75% of the assimilated carbon remained in the aboveground parts of the seedlings. The amount of carbon allocated to root and rhizosphere respiration was about 9–26%, and the amount of carbon allocated to root and ectomycorrhizal biomass about 13–21% of the total assimilated CO2. The 14CO2 pulse reached the root system within few hours after the labelling and most of the pulse had passed the root system after 48 h. The transport rate of carbon from shoot to roots was fastest in Silver birch seedlings.

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References

  • Arovaara H, Ilvesniemi H (1990) The effects of soluble inorganic aluminium and nutrient imbalances on Pinus sylvestris and Picea abies seedlings. In: Kauppi P, Kenttämies K, Anttila P (eds) Acidification in Finland. Springer, Berlin, pp 715–733

    Google Scholar 

  • Bowden RD, Nadelhoffer KJ, Boone RD, Melillo JM, Garrison JB (1993) Contributions of aboveground litter, belowground litter, and root respiration to total soil respiration in a temperate mixed hardwood forest. Can J For Res 23:1402–1407. doi:10.1139/x93-177

    Article  Google Scholar 

  • Bowling DR, Sargent SD, Tanner BD, Ehleringer JR (2003) Tunable diode laser absorption spectroscopy for stable isotope studies of ecosystem–atmosphere CO2 exchange. Agric For Meteorol 118:1–19. doi:10.1016/S0168-1923(03)00074-1

    Article  Google Scholar 

  • Buchmann N, Brooks JR, Ehleringer JR (2002) Predicting daytime carbon isotope ratios of atmospheric CO2 within forest canopies. Funct Ecol 16:49–57. doi:10.1046/j.0269-8463.2001.00591.x

    Article  Google Scholar 

  • Cajander AK (1949) Forest types and their significance. Acta For Fenn 56:1–71

    Google Scholar 

  • Chapin FS III, Matson PA, Mooney HA (1999) Gross primary production. In: Principles of terrestrial ecology. Springer, Berlin, pp 117

  • Davidson EA, Belk E, Boone RD (1998) Soil water content and temperature as independent or confounded factors controlling soil respiration in a temperate mixed hardwood forest. Glob Chang Biol 4:217–227. doi:10.1046/j.1365-2486.1998.00128.x

    Article  Google Scholar 

  • Ekblad A, Boström B, Holm A, Comstedt D (2005) Forest soil respiration rate and δ13C is regulated by recent above ground weather conditions. Oecologia 143:136–142. doi:10.1007/s00442-004-1776-z

    Article  PubMed  Google Scholar 

  • Ewel KC, Cropper WP Jr, Gholz HL (1987) Soil CO2 evolution in Florida slash pine plantations. II. Importance of root respiration. Can J For Res 17:330–333. doi:10.1139/x87-055

    Article  Google Scholar 

  • Gordon JC, Larson PR (1970) Redistribution of 14C labeled reserve food in young red pines during shoot elongation. For Sci 16(1):14–20

    Google Scholar 

  • Hanson PJ, Edwards NT, Garten CT, Andrews JA (2000) Separating root and soil microbial contributions to soil respiration: a review of methods and observations. Biogeochemistry 48:115–146. doi:10.1023/A:1006244819642

    Article  CAS  Google Scholar 

  • Heinonsalo J, Sen R (2007) Scots pine ectomycorrhizal fungi inoculum potential and dynamics in podzol-specific humus, eluvial and illuvial horizons one and four growth seasons after forest clear-cut logging. Can J For Res 37(2):404–414. doi:10.1139/X06-212

    Article  CAS  Google Scholar 

  • Heinonsalo J, Jørgensen K, Sen R (2001) Microcosm-based analyses of Scots pine seedling growth, ectomycorrhizal fungal community structure and bacterial carbon utilization profiles in boreal forest humus and underlying illuvial mineral horizons. FEMS Microbiol Ecol 35:73–84. doi:10.1111/j.1574-6941.2001.tb00827.x

    Google Scholar 

  • Heinonsalo J, Hurme K-R, Sen R (2004) Recent 14C-labelled assimilate allocation to Scots pine seedling root and mycorrhizosphere compartments developed on reconstructed podzol humus, E- and B-mineral horizons. Plant Soil 259(1):111–121. doi:10.1023/B:PLSO.0000020939.64205.c4

    Article  CAS  Google Scholar 

  • Högberg P, Read D (2006) Towards a more plant physiological perspective on soil ecology. Trends Ecol Evol 21(10):548–554. doi:10.1016/j.tree.2006.06.004

    Article  PubMed  Google Scholar 

  • Högberg P, Nordgren A, Buchmann N, Taylor AFS, Ekblad A, Högberg MN, Nyberg G, Ottosson-Löfvenius M, Read DJ (2001) Large-scale forest girdling shows that current photosynthesis drives soil respiration. Nature 411:789–792. doi:10.1038/35081058

    Article  PubMed  Google Scholar 

  • Kirschbaum MUF (1995) The temperature dependence of soil organic matter decomposition, and the effect of global warming on soil organic C storage. Soil Biol Biochem 27(6):753–760. doi:10.1016/0038-0717(94)00242-S

    Article  CAS  Google Scholar 

  • Knohl A, Werner RA, Brand WA, Buchmann N (2005) Short-term variations in δ13C of ecosystem respiration reveals link between assimilation and respiration in a deciduous forest. Ecosyst Ecol 142:70–82

    Google Scholar 

  • Konôpka B, Curiel JC, Janssens IA, Ceulemans R (2005) Comparison of fine root dynamics in Scots pine and pedunculate oak in sandy soil. Plant Soil 276:33–45. doi:10.1007/s11104-004-2976-3

    Article  Google Scholar 

  • Kozlowski TT (1992) Carbohydrate sources and sinks in woody-plants. Bot Rev 58(2):107–222. doi:10.1007/BF02858600

    Article  Google Scholar 

  • Kramer PJ, Kozlowski TT (1960) Physiology of Trees. McGraw-Hill, New York, p 338

    Google Scholar 

  • Kramer PJ, Kozlowski TT (1979) Physiology of woody plants. Academic Press, New York, pp 373–391, 445–493

  • Kuzyakov Y, Biryukova OV, Kuznetzova TV, Mölter K, Kandeler E, Stahr K (2002) Carbon partitioning in plant and soil, carbon dioxide fluxes and enzyme activities as affected by cutting ryegrass. Biol Fertil Soils 35:348–358. doi:10.1007/s00374-002-0480-6

    Article  CAS  Google Scholar 

  • Lippu J (1994) Patterns of dry matter partitioning and 14C-photosynthate allocation in 1.5-year-old Scots pine seedlings. Silva Fenn 28(3):145–153

    Google Scholar 

  • Maier CA, Kress LW (2000) Soil CO2 evolution and root respiration in 11-year-old loblolly pine (Pinus taeda) plantations as affected by moisture and nutrient availability. Can J For Res 30:347–359. doi:10.1139/cjfr-30-3-347

    Article  Google Scholar 

  • Nakane K, Yamamoto M, Tsubota H (1983) Estimation of root respiration rate in a mature forest ecosystem. Jpn J Ecol 33:397–408

    Google Scholar 

  • Nakane K, Kohno T, Horikoshi T (1996) Root respiration rate before and just after clear-felling in a mature, deciduous, broad-leaved forest. Ecol Res 11:111–119. doi:10.1007/BF02347678

    Article  Google Scholar 

  • Prescott CE, Zabek LM, Staley CL, Kabzems R (2000) Decomposition of broadleaf and needle litter in forests of British Columbia: influences of litter type, forest type, and litter mixtures. Can J For Res 30:1742–1750. doi:10.1139/cjfr-30-11-1742

    Article  Google Scholar 

  • Schneider A, Schmitz K (1989) Seasonal course of translocation and distribution of 14C-labelled photoassimilate in young trees of Larix decidua Mill. Trees (Berl) 4:185–191

    Google Scholar 

  • Thompson RG, Fensom DS, Anderson RR, Drouin R, Leiper W (1979) Translocation of 14C from leaves of Helianthus, Heracleum, Nymphoides, Ipomoea, Tropaeolum, Zea, Fraxinus, Ulmus, Picea and Pinus: comparative shapes and some fine structure profiles. Can J Bot 57:845–863. doi:10.1139/b79-106

    Article  Google Scholar 

  • Wu B, Nara K, Hogetsu T (2001) Can 14C-labeled photosynthetic products move between Pinus densiflora seedlings linked by ectomycorrhizal mycelia? New Phytol 149:137–146. doi:10.1046/j.1469-8137.2001.00010.x

    Article  CAS  Google Scholar 

  • Wu B, Nara K, Hogetsu T (2002) Spatiotemporal transfer of carbon-14-labelled photosynthate from ectomycorrhizal Pinus densiflora seedlings to extraradical mycelia. Mycorrhiza 12:83–88. doi:10.1007/s00572-001-0157-2

    Article  PubMed  CAS  Google Scholar 

  • Zimmermann MH (1958) Translocation of organic substances in the phloem of trees. In: Thiman KV (ed) The physiology of forest trees. Ronald Press, New York, pp 381–400

    Google Scholar 

Download references

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Correspondence to Jukka Sakari Pumpanen.

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Communicated by T. Hogetsu.

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Pumpanen, J.S., Heinonsalo, J., Rasilo, T. et al. Carbon balance and allocation of assimilated CO2 in Scots pine, Norway spruce, and Silver birch seedlings determined with gas exchange measurements and 14C pulse labelling. Trees 23, 611–621 (2009). https://doi.org/10.1007/s00468-008-0306-8

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  • DOI: https://doi.org/10.1007/s00468-008-0306-8

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