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Aspen shoots are carbon autonomous during bud break

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Abstract

Current thinking holds that carbon autonomy of branches in trees is unlikely, particularly during bud break, when the new developing shoots require significant influx of carbon resources from more distant sources. Results from recent studies indicate that the impact of bud break on overall tree reserves might be small. In two studies the independence of flushing shoots from stored carbon reserves and the photosynthesis in developing new leaves and shoots of Populus tremuloides were explored. New developing shoots quickly became a positive carbon source and only a few days into flush, the photosynthetic system of the newly developing shoots was efficient enough to achieve positive carbon gain even at low light levels. Only 14% of the stored shoot reserves, without any mobilization from more distant reserves, were used during bud break and early shoot expansion. Without any underlying stress, shoots of deciduous trees appear to be carbon autonomous during bud break when demand on stored carbon should be the highest. The development of an efficient photosynthetic system in new shoots is critical in the recovery of carbon reserves in aspen. It minimizes the cost of bud break to the overall stored carbon reserves by optimizing the assimilation of carbon in the newly developed leaves, while eliminating the cost for mobilizing carbon reserves from more distant sources. This carbon autonomy of shoots has important implications for the whole tree carbon balance particularly to the non-photosynthetic tissues which functions solely depending on carbon export from the newly developing leaves and shoots.

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References

  • Aschan G, Pfanz H (2003) Non-foliar photosynthesis–a strategy of additional carbon acquisition. Flora 198:81–97

    Google Scholar 

  • Aschan G, Wittmann C, Pfanz H (2001) Age-dependent bark photosynthesis of aspen twigs. TREES 15:431–437

    Article  Google Scholar 

  • Azcón-Bieto J, Osmond CB (1983) Relationship between photosynthesis and respiration. Plant Physiol 71:574–581

    Article  PubMed  Google Scholar 

  • Chapin FS, Schulze ED, Mooney HA (1990) The ecology and economics of storage in plants. Ann Rev Ecol Syst 21:423–447

    Article  Google Scholar 

  • Chow P, Landhäusser SM (2004) A simplified method for measuring sugar and starch content in woody-plant tissues. Tree Physiol 24:1129–1136

    PubMed  CAS  Google Scholar 

  • Dickmann DI (1971) Photosynthesis and respiration by developing leaves of cottonwood (Populus deltoides Bartr). Bot Gazette 132:253–259

    Article  Google Scholar 

  • Dickmann DI, Kozlowski TT (1970) Mobilization and incorporation of photoassimilated C14 by growing vegetative and reproductive tissue of adult Pinus resinosa AIT trees. Plant Physiol 45:284–288

    Article  PubMed  CAS  Google Scholar 

  • Gordon JC, Larson PR (1970) Redistribution of C14 labeled reserve food in young red pines during shoot elongation. For Sci 16:14–20

    Google Scholar 

  • Gratani L (1996) Leaf and shoot growth dynamics of Quercus ilex L. Acta Oecol Int J Ecol 17:17–27

    Google Scholar 

  • Hasegawa S, Koba K, Tayasu I, Takeda H, Haga H (2003) Carbon autonomy of reproductive shoots of Siberian alder (Alnus hirsuta var. sibirica). J Plant Res 116:183–188

    Article  PubMed  Google Scholar 

  • Hoch G (2005) Fruit-bearing branchlets are carbon autonomous in mature broad-leaved temperate forest trees. Plant Cell Environ 28:651–659

    Article  CAS  Google Scholar 

  • Hoch G, Keel SG (2006) C13 labelling reveals different contributions of photoassimilates from infructescences for fruiting in two temperate forest tree species. Plant Biol 8:606–614

    Article  PubMed  CAS  Google Scholar 

  • Imaji A, Seiwa K (2010) Carbon allocation to defense, storage, and growth in seedlings of two temperate broad-leaved tree species. Oecologia 162:273–281

    Article  PubMed  Google Scholar 

  • Kozlowski TT (1992) Carbohydrate sources and sinks in woody plants. Bot Rev 58:107–222

    Article  Google Scholar 

  • Kozlowski TT, Pallardy SG (2002) Acclimation and adaptive responses of woody plants to environmental stresses. Bot Rev 68:270–334

    Article  Google Scholar 

  • Landhäusser SM, Lieffers VJ (1998) Growth of Populus tremuloides in association with Calamagrostis canadensis. Can J For Res 28:396–401

    Article  Google Scholar 

  • Landhäusser SM, Lieffers VJ (2003) Seasonal changes in carbohydrate reserves in mature northern Populus tremuloides clones. TREES 17:471–476

    Google Scholar 

  • Landhäusser SM, Desrochers A, Lieffers VJ (2001) A comparison of growth and physiology in white spruce (Picea glauca) and aspen (Populus tremuloides) at different soil temperatures. Can J For Res 31:1922–1929

    Google Scholar 

  • Larson PR, Gordon JC (1969) Leaf development, photosynthesis, and C14 distribution in Populus deltoides seedlings. Am J Bot 56:1058–1066

    Article  CAS  Google Scholar 

  • Marchi S, Sebastiani L, Gucci R, Tognetti R (2005) Sink-source transition in peach leaves during shoot development. J Am Soc Hort Sci 130:928–935

    Google Scholar 

  • Martens L, Landhäusser SM, Lieffers VJ (2007) First-year growth response of cold-stored, nursery-grown aspen planting stock. New For 33:281–295

    Article  Google Scholar 

  • Newell EA, Mulkey SS, Wright SJ (2002) Seasonal patterns of carbohydrate storage in four tropical tree species. Oecologia 131:333–342

    Article  Google Scholar 

  • Potvin C, Lechowicz MJ, Tardif S (1990) The statistical analysis of ecophysiological response curves obtained from experiments involving repeated measures. Ecology 71:1389–1400

    Article  Google Scholar 

  • Protz CG, Silins U, Lieffers VJ (2000) Reduction in branch sapwood hydraulic permeability as a mechanism for crown recession in lodgepole pine. Can J For Res 30:1088–1095

    Article  Google Scholar 

  • Reiter IM, Haberle KH, Nunn AJ, Heerdt C, Reitmayer H, Grote R, Matyssek R (2005) Competitive strategies in adult beech and spruce: space-related foliar carbon investment versus carbon gain. Oecologia 146:337–349

    Article  PubMed  CAS  Google Scholar 

  • Schädel C, Blochl A, Richter A, Hoch G (2009) Short-term dynamics of nonstructural carbohydrates and hemicelluloses in young branches of temperate forest trees during bud break. Tree Physiol 29:901–911

    Article  PubMed  Google Scholar 

  • Sellin A, Kupper P (2005a) Variation in leaf conductance of silver birch: effects of irradiance, vapour pressure deficit, leaf water status and position within a crown. For Ecol Manage 206:153–166

    Article  Google Scholar 

  • Sellin A, Kupper P (2005b) Effects of light availability versus hydraulic constraints on stomatal responses within a crown of silver birch. Oecologia 142:388–397

    Article  PubMed  Google Scholar 

  • Sprugel DG (2002) When branch autonomy fails: Milton’s Law of resource availability and allocation. Tree Physiol 22:1119–1124

    PubMed  Google Scholar 

  • Sprugel DG, Hinckley TM (1988) The branch autonomy theory. In: Winner WE, Phelps LB (eds) Response of trees to air pollution: the role of branch studies. Proceedings of Workshop, November 5–6, 1987, Boulder, CO, pp 1–19

  • Sprugel DG, Hinckley TM, Schaap W (1991) The theory and practice of branch autonomy. Ann Rev Ecol Syst 22:309–334

    Article  Google Scholar 

  • Turgeon R (1989) The sink-source transition in leaves. Ann Rev Plant Physiol Plant Mol Biol 40:119–138

    Article  Google Scholar 

  • Volpe G, Bianco LB, Rieger M (2008) Carbon autonomy of peach shoots determined by C13-photoassimilate transport. Tree Physiol 28:1805–1812

    PubMed  CAS  Google Scholar 

Download references

Acknowledgments

I thank Alison Lennie and Ian Curran for their assistance with the physiological measurements and Pak Chow with the carbohydrate analyses. I thank Justine Karst for her comments on an earlier draft of this manuscript. This study has been supported by the Natural Sciences and Engineering Research Council of Canada (NSERC).

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Correspondence to Simon M. Landhäusser.

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Communicated by H. Rennenberg.

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Landhäusser, S.M. Aspen shoots are carbon autonomous during bud break. Trees 25, 531–536 (2011). https://doi.org/10.1007/s00468-010-0532-8

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  • DOI: https://doi.org/10.1007/s00468-010-0532-8

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