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Tree Size- and Age-Related Changes in Leaf Physiology and Their Influence on Carbon Gain

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Book cover Size- and Age-Related Changes in Tree Structure and Function

Part of the book series: Tree Physiology ((TREE,volume 4))

Abstract

Understanding how leaf-level physiology changes with tree size and age is important for scaling single leaf measurements to the whole plant and stand level and for quantifying carbon fluxes from forest ecosystems. This chapter reviews what is known about the influences of tree height and age on gas exchange and foliar structure in both gymnosperm and angiosperm trees. We address how the key physiological processes, photosynthesis, respiration and stomatal conductance vary with tree height and age. To help explain the observed patterns, the underlying factors that can be responsible for the changes in leaf physiology are assessed, including tree size- and age-related trends in foliar anatomy, morphology and chemistry. In addition to modifications in foliar morphology and chemistry, biochemical limitations to net assimilation rates associated with the diffusion of carbon dioxide from the atmosphere to the sites of carboxylation are examined. Our review emphasizes that a variety of factors collectively are responsible for tree height- and age-related decline in net photosynthetic rates, and that the importance of different limitations varies for different species and between gymnosperm and angiosperm trees. While there is still much to be learned, what is clear from our current understanding is that more integrated studies that consider the simultaneous roles of leaf structure, chemistry and stomatal and mesophyll factors are needed to disentangle and assign importance to the various factors responsible for decreases in carbon gain with tree age and size.

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References

  • Abdul-Hamid H, Mencuccini M (2009) Age- and size-related changes in physiological characteristics and chemical composition of Acer pseudoplatanus and Fraxinus excelsior trees. Tree Physiol 29:27–38

    Article  PubMed  Google Scholar 

  • Ambrose AR, Sillett SC, Dawson TE (2009) Effects of tree height on branch hydraulics, leaf structure and gas exchange in California redwoods. Plant Cell Environ 32:743–757

    Article  PubMed  Google Scholar 

  • Apple M, Tiekotter K, Snow M, Young J, Soeldner A, Phillips D, Tingey D, Bond BJ (2002) Needle anatomy changes with increasing tree age in Douglas-fir. Tree Physiol 22:129–136

    PubMed  Google Scholar 

  • Ball JT, Berry JA (1982) The Ci/Cs ratio: a basis for predicting stomatal control of photosynthesis. Carnegie Inst Wash Yearb 81:88–92

    Google Scholar 

  • Bond BJ (2000) Age-related changes in photosynthesis of woody plants. Trends Plant Sci 5:349–353

    Article  PubMed  CAS  Google Scholar 

  • Bond BJ, Czarnomski NM, Cooper C, Day ME, Greenwood MS (2007) Developmental decline in height growth in Douglas-fir. Tree Physiol 27:441–453

    PubMed  Google Scholar 

  • Brett CT, Waldron KW (1996) Physiology and biochemistry of plant cell walls, vol 1, 2nd edn, Topics in plant functional biology. Chapman and Hall, London, 225 pp

    Google Scholar 

  • Burghardt M, Riederer M (2006) Cuticular transpiration. In: Riederer M, Müller C (eds) Biology of the plant cuticle. Blackwell, Oxford, pp 292–311

    Chapter  Google Scholar 

  • Day ME, Greenwood MS, White AS (2001) Age-related changes in foliar morphology and physiology in red spruce and their influence on declining photosynthetic rates and productivity with tree age. Tree Physiol 21:1195–1204

    PubMed  CAS  Google Scholar 

  • DeLucia EH, Berlyn GP (1984) The effect of increasing elevation on leaf cuticle thickness and cuticular transpiration in balsam fir. Can J Bot 62:2423–2431

    Article  Google Scholar 

  • Donovan LA, Ehleringer JR (1991) Ecophysiological differences among juvenile and reproductive plants of several woody species. Oecologia 86:594–597

    Article  Google Scholar 

  • Donovan LA, Ehleringer JR (1992) Contrasting water-use patterns among size and life-history classes of a semi-arid shrub. Funct Ecol 6:482–488

    Article  Google Scholar 

  • England JR, Attiwill PM (2006) Changes in leaf morphology and anatomy with tree age and height in the broadleaved evergreen species, Eucalyptus regnans F. Muell. Trees 20:79–90

    Article  Google Scholar 

  • Evans JR, Kaldenhoff R, Terashima I (2009) Resistances along the CO2 diffusion pathway inside leaves. J Exp Bot 60:2235–2248

    Article  PubMed  CAS  Google Scholar 

  • Fischer DG, Kolb TE, De Wald LE (2002) Changes in whole-tree water relations during ontogeny of Pinus flexilis and Pinus ponderosa in a high-elevation meadow. Tree Physiol 22:675–685

    PubMed  Google Scholar 

  • Fredericksen TS, Steiner KC, Skelly JM, Joyce BJ, Kolb TE, Kouterick KB, Ferdinand JA (1996) Diel and seasonal patterns of leaf gas exchange and xylem water potentials of different-sized Prunus serotina Ehrh. trees. For Sci 42:359–365

    Google Scholar 

  • Gower ST, McMurtrie RE, Murty D (1996) Aboveground net primary production decline with stand age: potential causes. Trends Ecol Evol 11:378–382

    Article  PubMed  CAS  Google Scholar 

  • Greenwood MS (1984) Phase change in loblolly pine: shoot development as a function of age. Physiol Plant 61:518–522

    Article  Google Scholar 

  • Greenwood MS, Ward MH, Day ME, Adams SL, Bond BJ (2008) Age-related trends in red spruce foliar plasticity in relation to declining productivity. Tree Physiol 28:225–232

    PubMed  CAS  Google Scholar 

  • Grulke NE, Retzlaff WA (2001) Changes in physiological attributes of ponderosa pine from seedling to mature tree. Tree Physiol 21:275–286

    PubMed  CAS  Google Scholar 

  • Herbinger K, Then C, Löw M, Haberer K, Alexous M, Koch N, Remele K, Heerdt C, Grill D, Rennenberg H, Häberle K-H, Matyssek R, Tausz M, Wieser G (2005) Tree age dependence and within-canopy variation of leaf gas exchange and antioxidative defence in Fagus sylvatica under experimental free-air ozone exposure. Environ Pollut 137:476–482

    Article  PubMed  CAS  Google Scholar 

  • Hubbard RM, Bond BJ, Ryan MG (1999) Evidence that hydraulic conductance limits photosynthesis in old Pinus ponderosa trees. Tree Physiol 19:165–172

    PubMed  Google Scholar 

  • Hutchison KW, Sherman CD, Weber J, Smith SS, Singer PB, Greenwood MS (1990) Maturation in larch. II. Effects of age on photosynthesis and gene expression in developing foliage. Plant Physiol 94:1308–1315

    Article  PubMed  CAS  Google Scholar 

  • Ishii H (2011) How do changes in leaf/shoot morphology and crown architecture affect growth and physiological function of large, old trees? In: Meinzer FC, Lachenbruch B, Dawson TE (eds.) Size- and age-related changes in tree structure and function. Springer, Dordrecht

    Google Scholar 

  • Juárez-López FJ, Escudero A, Mediavilla S (2008) Ontogenetic changes in stomatal and biochemical limitations to photosynthesis of two co-occurring Mediterranean oaks differing in leaf life span. Tree Physiol 28:367–374

    PubMed  Google Scholar 

  • Kenzo T, Ichie T, Watanabe Y, Yoneda R, Ninomiya I, Koike T (2006) Changes in photosynthesis and leaf characteristics with tree height in five dipterocarp species in a tropical rain forest. Tree Physiol 26:865–873

    PubMed  CAS  Google Scholar 

  • Koch GW, Sillett SC, Jennings GM, Davis SD (2004) The limits to tree height. Nature 428:851–854

    Article  PubMed  CAS  Google Scholar 

  • Koike T (1984) Comparison of photosynthetic response to habitat factors between seedlings and saplings of Fraxinus mandshurica var. japonica. Environ Control Biol 22:33–38

    CAS  Google Scholar 

  • Koike T, Sakagami Y, Fujimura Y (1986) Characteristics of the leaf dynamics and the photosynthesis of the seedlings and saplings of Betula maximowicziana and Fraxinus mandshurica var. japonica in Hokkaido, Japan. In: Fujimori T, Whitehead D (eds) Crown and canopy structure in relation to productivity. Forestry and Forest Products Research Institute, Ibraki, pp 396–408

    Google Scholar 

  • Köstner B, Falge E, Tenhunen JD (2002) Age-related effects on leaf area/sapwood area relationships, canopy transpiration and carbon gain of Norway spruce stands (Picea abies) in the Fichtelgebirge, Germany. Tree Physiol 22:567–574

    PubMed  Google Scholar 

  • Kozlowski TT (1971) Seed germination, ontogeny and shoot growth. In: Growth and development of trees, Vol 1. Academic, New York, 443 pp

    Google Scholar 

  • Kull O, Koppel A (1987) Net photosynthetic response to light intensity of shoots from different crown positions and age in Picea abies (L.) Karst. Scand J Forest Res 2:157–166

    Article  Google Scholar 

  • Lockhart JA (1965) An analysis of irreversible plant cell elongation. J Theor Biol 8:264–275

    Article  PubMed  CAS  Google Scholar 

  • Magnani F, Bensada A, Cinnirella S, Ripullone F, Borghetti M (2008) Hydraulic limitations and water-use efficiency in Pinus pinaster along a chronosequence. Can J For Res 38:73–81

    Article  Google Scholar 

  • Malkina IS (1983) Relationships between photosynthesis of oak leaves and their structure and age of trees. Lesovedeniye 4:68–71

    Google Scholar 

  • Martínez-Vilalta J, Vanderklein D, Mencuccini M (2007) Tree height and age-related decline in growth in Scots pine (Pinus sylvestris L.). Oecologia 150:529–544

    Article  PubMed  Google Scholar 

  • McDowell NG, Licata J, Bond BJ (2005) Environmental sensitivity of gas exchange in different-sized trees. Oecologia 145:9–20

    Article  PubMed  Google Scholar 

  • McDowell NG, Bond BJ, Hill LT, Ryan MG, Whitehead D (2011) Relationships between tree height and carbon isotope discrimination. In: Meinzer FC, Lachenbruch B, Dawson TE (eds.) Size- and age-related changes in tree structure and function. Springer, Dordrecht

    Google Scholar 

  • Mencuccini M (2002) Hydraulic constraints in the functional scaling of trees. Tree Physiol 22:553–565

    PubMed  Google Scholar 

  • Mencuccini M, Martínez-Vilalta J, Hamid HA, Korakaki E, Vanderklein D (2007) Evidence for age- and size-mediated controls of tree growth from grafting studies. Tree Physiol 27:463–473

    PubMed  Google Scholar 

  • Merilo E, Tulva I, Räim O, Kükit A, Sellin A, Kull O (2009) Changes in needle nitrogen partitioning and photosynthesis during 80 years of tree ontogeny in Picea abies. Trees 23:951–958

    Article  Google Scholar 

  • Mullin LP, Sillett SC, Koch GW, Tu KP, Antoine ME (2009) Physiological consequences of height-related morphological variation in Sequoia sempervirens foliage. Tree Physiol 29:999–1010

    Article  PubMed  Google Scholar 

  • Nabeshima E, Hiura T (2004) Size dependency of photosynthetic water- and nitrogen-use efficiency and hydraulic limitation in Acer mono. Tree Physiol 24:745–752

    PubMed  Google Scholar 

  • Nabeshima E, Hiura T (2008) Size-dependency in hydraulic and photosynthetic properties of three Acer species having different maximum sizes. Ecol Res 23:281–288

    Article  CAS  Google Scholar 

  • Niinemets Ü (1997a) Distribution patterns of foliar carbon and nitrogen as affected by tree dimensions and relative light conditions in the canopy of Picea abies. Trees 11:144–154

    Google Scholar 

  • Niinemets Ü (1997b) Energy requirement for foliage construction depends on tree size in young Picea abies trees. Trees 11:420–431

    Google Scholar 

  • Niinemets Ü (1999) Research review. Components of leaf dry mass per area, thickness and density alter leaf photosynthetic capacity in reverse directions in woody plants. New Phytol 144:35–47

    Article  Google Scholar 

  • Niinemets Ü (2001) Climatic controls of leaf dry mass per area, density and thickness in trees and shrubs at the global scale. Ecology 82:453–469

    Article  Google Scholar 

  • Niinemets Ü (2002) Stomatal conductance alone does not explain the decline in foliar photosynthetic rates with increasing tree age and size in Picea abies and Pinus sylvestris. Tree Physiol 22:515–535

    PubMed  Google Scholar 

  • Niinemets Ü (2010) Responses of forest trees to single and multiple environmental stresses from seedlings to mature plants: past stress history, stress interactions, tolerance and acclimation. For Ecol Manag 260:1623–1639

    Article  Google Scholar 

  • Niinemets Ü, Kull O (1995) Effects of light availability and tree size on the architecture of assimilative surface in the canopy of Picea abies: variation in needle morphology. Tree Physiol 15:307–315

    PubMed  Google Scholar 

  • Niinemets Ü, Sack L (2006) Structural determinants of leaf light-harvesting capacity and photosynthetic potentials. In: Esser K, Lüttge UE, Beyschlag W, Murata J (eds) Progress in botany, vol 67. Springer Verlag, Berlin, pp 385–419

    Chapter  Google Scholar 

  • Niinemets Ü, Tenhunen JD (1997) A model separating leaf structural and physiological effects on carbon gain along light gradients for the shade-tolerant species Acer saccharum. Plant Cell Environ 20:845–866

    Article  Google Scholar 

  • Niinemets Ü, Kull O, Tenhunen JD (1999) Variability in leaf morphology and chemical composition as a function of canopy light environment in co-existing trees. Int J Plant Sci 160:837–848

    Article  PubMed  Google Scholar 

  • Niinemets Ü, Díaz-Espejo A, Flexas J, Galmés J, Warren CR (2009) Role of mesophyll diffusion conductance in constraining potential photosynthetic productivity in the field. J Exp Bot 60:2249–2270

    Article  PubMed  CAS  Google Scholar 

  • Nobel PS (1991) Physicochemical and environmental plant physiology, 4th edn. Academic, New York

    Google Scholar 

  • Poorter H, Niinemets Ü, Poorter L, Wright IJ, Villar R (2009) Causes and consequences of variation in leaf mass per area (LMA): a meta-analysis. New Phytol 182:565–588

    Article  PubMed  Google Scholar 

  • Rebbeck J, Jensen KF, Greenwood MS (1992) Ozone effects on the growth of grafted mature and juvenile red spruce. Can J For Res 22:756–760

    Article  CAS  Google Scholar 

  • Richardson AD, Berlyn GP, Ashton PMS, Thadani R, Cameron IR (2000) Foliar plasticity of hybrid spruce in relation to crown position and stand age. Can J Bot 78:305–317

    Google Scholar 

  • Rijkers T, Pons TL, Bongers F (2000) The effect of tree height and light availability on photosynthetic leaf traits of four neotropical species differing in shade tolerance. Funct Ecol 14:77–86

    Article  Google Scholar 

  • Ryan MG, Yoder BJ (1997) Hydraulic limits to tree height and tree growth. What keeps trees from growing beyond a certain height? Bioscience 47:235–242

    Article  Google Scholar 

  • Ryan MG, Binkley D, Fownes JH (1997) Age-related decline in forest productivity: pattern and process. Adv Ecol Res 27:213–262

    Article  Google Scholar 

  • Saveyn A, Steppe K, Lemeur R (2007) Daytime depression in tree stem CO2 efflux rates: is it caused by low stem turgor pressure? Ann Bot 99:477–485

    Article  PubMed  CAS  Google Scholar 

  • Schoettle AW (1994) Influence of tree size on shoot structure and physiology of Pinus contorta and Pinus aristata. Tree Physiol 14:1055–1068

    PubMed  Google Scholar 

  • Sinnott EW (1960) Plant morphogenesis. McGraw-Hill, New York, 550 pp

    Google Scholar 

  • Slaton MR, Hunt ER, Smith WK (2001) Estimating near-infrared leaf reflectance from leaf structural characteristics. Am J Bot 88:278–284

    Article  PubMed  CAS  Google Scholar 

  • Steppe K, De Pauw DJW, Lemeur R, Vanrolleghem PA (2006) A mathematical model linking tree sap flow dynamics to daily stem diameter fluctuations and radial stem growth. Tree Physiol 26:257–273

    Article  PubMed  Google Scholar 

  • Terashima I, Araya T, Miyazawa S-I, Sone K, Yano S (2005) Construction and maintenance of the optimal photosynthetic systems of the leaf, herbaceous plant and tree: an eco-developmental treatise. Ann Bot 95:507–519

    Article  PubMed  CAS  Google Scholar 

  • Vanderklein D, Marinez-Vilalta J, Lee S, Mencuccini M (2007) Plant size, not age, regulates growth and gas exchange in grafted Scots pine trees. Tree Physiol 27:71–79

    PubMed  CAS  Google Scholar 

  • Wong SC, Cowan IR, Farquhar GD (1979) Stomatal conductance correlates with photosynthetic capacity. Nature 282:424–426

    Article  Google Scholar 

  • Wong S-C, Cowan IR, Farquhar GD (1985) Leaf conductance in relation to rate of CO2 assimilation. III. Influences of water stress and photoinhibition. Plant Physiol 78:830–834

    Article  PubMed  CAS  Google Scholar 

  • Woodruff DR, Meinzer FC (2011) Size-dependent changes in biophysical control of tree growth: the role of turgor. In: Meinzer FC, Lachenbruch B, Dawson TE (eds.) Size- and age-related changes in tree structure and function. Springer, Dordrecht

    Google Scholar 

  • Woodruff DR, Bond BJ, Meinzer FC (2004) Does turgor limit growth in tall trees? Plant Cell Environ 27:229–236

    Article  Google Scholar 

  • Woodruff DR, McCulloh KA, Warren JM, Meinzer FC, Lachenbruch B (2007) Impacts of tree height on leaf hydraulic architecture and stomatal control in Douglas-fir. Plant Cell Environ 30:559–569

    Article  PubMed  Google Scholar 

  • Woodruff DR, Meinzer FC, Lachenbruch B (2008) Height-related trends in leaf xylem anatomy and shoot hydraulic characteristics in a tall conifer: safety versus efficiency in water transport. New Phytol 180:90–99

    Article  PubMed  CAS  Google Scholar 

  • Woodruff DR, Meinzer FC, Lachenbruch B, Johnson DM (2009) Coordination of leaf structure and gas exchange along a height gradient in a tall conifer. Tree Physiol 29:261–272

    Article  PubMed  CAS  Google Scholar 

  • Woodruff DR, Meinzer FC, McCulloh KA (2010) Height-related trends in stomatal sensitivity to leaf-to-air vapour pressure deficit in a tall conifer. J Exp Bot 61:203–210

    Article  PubMed  CAS  Google Scholar 

  • Wright IJ, Reich PB, Westoby M, Ackerly DD, Baruch Z, Bongers F, Cavender-Bares J, Chapin T, Cornelissen JHC, Diemer M, Flexas J, Garnier E, Groom PK, Gulias J, Hikosaka K, Lamont BB, Lee T, Lee W, Lusk C, Midgley JJ, Navas ML, Niinemets Ü, Oleksyn J, Osada N, Poorter H, Poot P, Prior L, Pyankov VI, Roumet C, Thomas SC, Tjoelker MG, Veneklaas E, Villar R (2004) The world-wide leaf economics spectrum. Nature 428:821–827

    Article  PubMed  CAS  Google Scholar 

  • Yoder BJ, Ryan MG, Waring RH, Schoettle AW, Kaufmann MR (1994) Evidence of reduced photosynthetic rates in old trees. For Sci 40:513–527

    Google Scholar 

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Steppe, K., Niinemets, Ü., Teskey, R.O. (2011). Tree Size- and Age-Related Changes in Leaf Physiology and Their Influence on Carbon Gain. In: Meinzer, F., Lachenbruch, B., Dawson, T. (eds) Size- and Age-Related Changes in Tree Structure and Function. Tree Physiology, vol 4. Springer, Dordrecht. https://doi.org/10.1007/978-94-007-1242-3_9

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