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A review of light interception in plant stands from leaf to canopy in different plant functional types and in species with varying shade tolerance

  • Special Feature
  • Plant responses to heterogeneous environments
  • Published:
Ecological Research

Abstract

Changes in the efficiency of light interception and in the costs for light harvesting along the light gradients from the top of the plant canopy to the bottom are the major means by which efficient light harvesting is achieved in ecosystems. In the current review analysis, leaf, shoot and canopy level determinants of plant light harvesting, the light-driven plasticity in key traits altering light harvesting, and variations among different plant functional types and between species of different shade tolerance are analyzed. In addition, plant age- and size-dependent alterations in light harvesting efficiency are also examined. At the leaf level, the variations in light harvesting are driven by alterations in leaf chlorophyll content modifies the fraction of incident light harvested by given leaf area, and in leaf dry mass per unit area (M A) that determines the amount of leaf area formed with certain fraction of plant biomass in the leaves. In needle-leaved species with complex foliage cross-section, the degree of foliage surface exposure also depends on the leaf total-to-projected surface area ratio. At the shoot scale, foliage inclination angle distribution and foliage spatial aggregation are the major determinants of light harvesting, while at the canopy scale, branching frequency, foliage distribution and biomass allocation to leaves (F L) modify light harvesting significantly. F L decreases with increasing plant size from herbs to shrubs to trees due to progressively larger support costs in plant functional types with greater stature. Among trees, F L and stand leaf area index scale positively with foliage longevity. Plant traits altering light harvesting have a large potential to adjust to light availability. Chlorophyll per mass increases, while M A, foliage inclination from the horizontal and degree of spatial aggregation decrease with decreasing light availability. In addition, branching frequency decreases and canopies become flatter in lower light. All these plastic modifications greatly enhance light harvesting in low light. Species with greater shade tolerance typically form a more extensive canopy by having lower M A in deciduous species and enhanced leaf longevity in evergreens. In addition, young plants of shade tolerators commonly have less strongly aggregated foliage and flatter canopies, while in adult plants partly exposed to high light, higher shade tolerance of foliage allows the shade tolerators to maintain more leaf layers, resulting in extended crowns. Within a given plant functional type, increases in plant age and size result in increases in M A, reductions in F L and increases in foliage aggregation, thereby reducing plant leaf area index and the efficiency of light harvesting. Such dynamic modifications in plant light harvesting play a key role in stand development and productivity. Overall, the current review analysis demonstrates that a suite of chemical and architectural traits at various scales and their plasticity drive plant light harvesting efficiency. Enhanced light harvesting can be achieved by various combinations of traits, and these suites of traits vary during plant ontogeny.

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References

  • Aan A, Hallik L, Kull O (2006) Photon flux partitioning among species along a productivity gradient of an herbaceous plant community. J Ecol 94:1143–1155

    Google Scholar 

  • Albaugh TJ, Allen HL, Dougherty PM, Kress LW, King JS (1998) Leaf area and above- and belowground growth responses of loblolly pine to nutrient and water additions. For Sci 44:317–328

    Google Scholar 

  • Ali MS, Kikuzawa K (2005) Plasticity in leaf-area density within the crown of Aucuba japonica growing under different light levels. J Plant Res 118:307–316

    PubMed  Google Scholar 

  • Anderson JM, Osmond CB (1987) Shade-sun response: compromises between acclimation and photoinhibition. In: Kyle DJ, Osmond CB, Arntzen CJ (eds) Photoinhibition. Elsevier, Amsterdam, pp 1–38

    Google Scholar 

  • Andersson F (1973) IBP-studies on plant productivity of south Swedish forest ecosystems. In: Kern L (ed) Modeling forest ecoystems, Report EDFB-IBP-73-7. Oak Ridge National Laboratory, Oak Ridge, pp 11–26

    Google Scholar 

  • Ando T (1981) IBP woodlands data set. In: Reichle DE (ed) Dynamic properties of forest ecosystems, IBP 23. Cambridge University Press, Cambridge, pp 604–605

    Google Scholar 

  • Anten NPR, Hirose T (1998) Biomass allocation and light partitioning among dominant and subordinate individuals in Xanthium canadense stands. Ann Bot 82:665–673

    Google Scholar 

  • Baldocchi DD, Hutchison BA, Matt DR, McMillen RT (1985) Canopy radiative transfer models for spherical and known leaf inclination angle distributions: a test in an oak-hickory forest. J Appl Ecol 22:539–555

    Google Scholar 

  • Baltzer JL, Thomas SC (2007) Physiological and morphological correlates of whole-plant light compensation point in temperate deciduous tree seedlings. Oecologia 153:209–223

    CAS  PubMed  Google Scholar 

  • Banez G, Gyokusen K, Saito A (1999) Plasticity in the branching characteristics of four year old Quercus acutissima and Q. serrata seedlings in response to low light intensity and additional fertilizer. Bull Kyushu Univ For 80:27–39

    Google Scholar 

  • Barclay HJ, Goodman D (2000) Conversion of total to projected leaf area index in conifers. Can J Bot 78:447–454

    Google Scholar 

  • Barker M, Van Miegroet H, Nicholas NS, Creed IF (2002) Variation in overstory nitrogen uptake in a small, high-elevation southern Appalachian spruce–fir watershed. Can J For Res 32:1741–1752

    Google Scholar 

  • Bartelink HH (1998) A model of dry matter partitioning in trees. Tree Physiol 18:91–101

    PubMed  Google Scholar 

  • Bassi R, Caffarri S (2000) Lhc proteins and the regulation of photosynthetic light harvesting function by xanthophylls. Photosynth Res 64:243–256

    CAS  PubMed  Google Scholar 

  • Bégin C, Filion L (1999) Black spruce (Picea mariana) architecture. Can J Bot 77:664–672

    Google Scholar 

  • Bégué A, Hanan NP, Prince SD (1994) Radiative transfer in shrub savanna sites in Niger: preliminary results from HAPEX-Sahel. 2. Photosynthetically active radiation interception of the woody layer. Agric For Meteorol 69:247–266

    Google Scholar 

  • Bindiu C (1981) IBP woodlands data set. In: Reichle DE (ed) Dynamic properties of forest ecosystems, IBP 23. Cambridge University Press, Cambridge, p 614

    Google Scholar 

  • Bloor JMG, Grubb PJ (2004) Morphological plasticity of shade-tolerant tropical rainforest tree seedlings exposed to light changes. Funct Ecol 18:337–348

    Google Scholar 

  • Bond BJ, Farnsworth BT, Coulombe RA, Winner WE (1999) Foliage physiology and biochemistry in response to light gradients in conifers with varying shade tolerance. Oecologia 120:183–192

    Google Scholar 

  • Bond-Lamberty B, Wang C, Gower ST, Norman J (2002) Leaf area dynamics of a boreal black spruce fire chronosequence. Tree Physiol 22:993–1001

    CAS  PubMed  Google Scholar 

  • Borchert R, Slade NA (1981) Bifurcation ratios and the adaptive geometry of trees. Bot Gaz 142:394–401

    Google Scholar 

  • Borghetti M, Vendramin GG, Giannini R (1986) Specific leaf area and leaf area distribution in a young Douglas-fir plantation. Can J For Res 16:1283–1288

    Google Scholar 

  • Cai Z-Q, Poorter L, Cao KF, Bongers F (2007) Seedling growth strategies in Bauhinia species: comparing lianas and trees. Ann Bot 100:831–838

    CAS  PubMed  Google Scholar 

  • Campbell GS (1986) Extinction coefficients for radiation in plant canopies calculated using an ellipsoidal inclination angle distribution. Agric For Meteorol 36:317–321

    Google Scholar 

  • Cescatti A (1997) Modelling the radiative transfer in discontinuous canopies of asymmetric crowns. II. Model testing and application in a Norway spruce stand. Ecol Model 101:275–284

    Google Scholar 

  • Cescatti A, Niinemets Ü (2004) Sunlight capture. Leaf to landscape. In: Smith WK, Vogelmann TC, Chritchley C (eds) Photosynthetic adaptation: chloroplast to landscape. Springer, Berlin, pp 42–85

    Google Scholar 

  • Cescatti A, Zorer R (2003) Structural acclimation and radiation regime of silver fir (Abies alba Mill.) shoots along a light gradient. Plant Cell Environ 26:429–442

    Google Scholar 

  • Chen JM (1996) Optically-based methods for measuring seasonal variation of leaf area index in boreal conifer stands. Agric For Meteorol 80:135–163

    Google Scholar 

  • Chen HYH (1997) Interspecific responses of planted seedlings to light availability in interior British Columbia: survival, growth, allometric patterns, and specific leaf area. Can J For Res 27:1383–1393

    Google Scholar 

  • Chen X, Vierling L, Deering D (2005) A simple and effective radiometric correction method to improve landscape change detection across sensors and across time. Remote Sens Environ 98:63–79

    Google Scholar 

  • Ciganda V, Gitelson A, Schepers J (2008) Vertical profile and temporal variation of chlorophyll in maize canopy: quantitative “crop vigor” indicator by means of reflectance-based techniques. Agron J 100:1409–1417

    CAS  Google Scholar 

  • Classen AT, Chapman SK, Whitham TG, Hart SC, Koch GW (2007) Genetic-based plant resistance and susceptibility traits to herbivory influence needle and root litter nutrient dynamics. J Ecol 95:1181–1194

    Google Scholar 

  • Claveau Y, Messier C, Comeau PG (2005) Interacting influence of light and size on aboveground biomass distribution in sub-boreal conifer saplings with contrasting shade tolerance. Tree Physiol 25:373–384

    PubMed  Google Scholar 

  • Cordell S, Goldstein G, Meinzer FC, Vitousek PM (2001) Regulation of leaf life-span and nutrient-use efficiency of Metrosideros polymorpha trees at two extremes of a long chronosequence in Hawaii. Oecologia 127:198–206

    Google Scholar 

  • Dahlberg U, Berge TW, Petersson H, Vencatasawmy CP (2004) Modelling biomass and leaf area index in a sub-arctic Scandinavian mountain area. Scand J For Res 19:60–71

    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

    CAS  PubMed  Google Scholar 

  • Deblonde G, Penner M, Royer A (1994) Measuring leaf area index with the LI-COR LAI-2000 in pine stands. Ecology 75:1507–1511

    Google Scholar 

  • Delagrange S, Messier C, Lechowicz MJ, Dizengremel P (2004) Physiological, morphological and allocational plasticity in understory deciduous trees: importance of plant size and light availability. Tree Physiol 24:775–784

    PubMed  Google Scholar 

  • Delzon S, Loustau D (2005) Age-related decline in stand water use: sap flow and transpiration in a pine forest chronosequence. Agric For Meteorol 129:105–119

    Google Scholar 

  • Demmig-Adams B, Adams WW III (2006) Photoprotection in an ecological context: the remarkable complexity of thermal energy dissipation. Tansley review. New Phytol 172:11–21

    Google Scholar 

  • Diggle PK (1999) Heteroblasty and the evolution of flowering phenologies. Int J Plant Sci 160:S123–S134

    PubMed  Google Scholar 

  • Duursma RA, Mäkelä A (2007) Summary models for light interception and light-use efficiency of non-homogeneous canopies. Tree Physiol 27:859–870

    CAS  PubMed  Google Scholar 

  • Ellsworth DS, Reich PB (1993) Canopy structure and vertical patterns of photosynthesis and related leaf traits in a deciduous forest. Oecologia 96:169–178

    Google Scholar 

  • Evans JR (1993) Photosynthetic acclimation and nitrogen partitioning within a lucerne canopy. I. Canopy characteristics. Aust J Plant Physiol 20:55–67

    CAS  Google Scholar 

  • Evans JR, Poorter H (2001) Photosynthetic acclimation of plants to growth irradiance: the relative importance of specific leaf area and nitrogen partitioning in maximizing carbon gain. Plant Cell Environ 24:755–767

    CAS  Google Scholar 

  • Falster DS, Westoby M (2003) Leaf size and angle vary widely across species: what consequences for light interception? New Phytol 158:509–525

    Google Scholar 

  • Farque L, Sinoquet H, Colin F (2001) Canopy structure and light interception in Quercus petraea seedlings in relation to light regime and plant density. Tree Physiol 21:1257–1267

    CAS  PubMed  Google Scholar 

  • Fassnacht KS, Gower ST (1997) Interrelationships among the edaphic and stand characteristics, leaf area index, and aboveground net primary production of upland forest ecosystems in north central Wisconsin. Can J For Res 27:1058–1067

    Google Scholar 

  • Fassnacht KS, Gower ST, Norman JM, McMurtrie RE (1994) A comparison of optical and direct methods for estimating foliage surface area index in forests. Agric For Meteorol 71:183–207

    Google Scholar 

  • Fisher JB (1986) Branching patterns and angles in trees. In: Givnish TJ (ed) On the economy of plant form and function. Proceedings of the sixth Maria Moors Cabot symposium. Evolutionary constraints on primary productivity: adaptive patterns of energy capture in plants. Harvard Forest, August 1983. Cambridge University Press, Cambridge, pp 493–523

  • Fleck S (2003) Integrated analysis of relationships between 3D-structure, leaf photosynthesis and branch transpiration of mature Fagus sylvatica and Quercus petraea trees in a mixed forest stand. BITÖK, Bayreuth

    Google Scholar 

  • Fleck S, Niinemets Ü, Cescatti A, Tenhunen JD (2003) Three-dimensional lamina architecture alters light harvesting efficiency in Fagus: a leaf-scale analysis. Tree Physiol 23:577–589

    PubMed  Google Scholar 

  • Fliervoet LM, Werger JA (1984) Canopy structure and microclimate of two wet grassland communities. New Phytol 96:115–130

    Google Scholar 

  • Frazer GW, Trofymow JA, Lertzman KP (2000) Canopy openness and leaf area in chronosequences of coastal temperate rainforests. Can J For Res 30:239–256

    Google Scholar 

  • Gersonde R, Battles JJ, O’Hara KL (2004) Characterizing the light environment in Sierra Nevada mixed-conifer forests using a spatially explicit light model. Can J For Res 34:1332–1342

    Google Scholar 

  • Gholz HL (1982) Environmental limits on aboveground net primary production, leaf area, and biomass in vegetation zones of the Pacific Northwest. Ecology 63:469–481

    Google Scholar 

  • Gholz HL, Vogel SA, Cropper WP Jr, McKelvey K, Ewel KC, Teskey RO, Curran PJ (1991) Dynamics of canopy structure and light interception in Pinus elliottii stands, North Florida. Ecol Monogr 61:33–51

    Google Scholar 

  • Givnish T (1979) On the adaptive significance of leaf form. In: Solbrig OT, Jain S, Johnson GB, Raven PH (eds) Topics in plant population biology. Columbia University Press, New York, pp 375–407

    Google Scholar 

  • Givnish TJ (1982) On the adaptive significance of leaf height in forest herbs. Am Nat 120:353–381

    Google Scholar 

  • Givnish TJ (1988) Adaptation to sun and shade: a whole-plant perspective. Aust J Plant Physiol 15:63–92

    Google Scholar 

  • Givnish TJ (2002) Adaptive significance of evergreen versus deciduous leaves: solving the triple paradox. Silva Fenn 36:703–743

    Google Scholar 

  • Givnish TJ, Vermeij GJ (1976) Sizes and shapes of liana leaves. Am Nat 110:743–776

    Google Scholar 

  • Gordon AG (1976) Taxonomy and genetics of Picea rubens and its relationship to Picea mariana. Can J Bot 54:781–813

    Google Scholar 

  • Gould KS (1993) Leaf heteroblasty in Pseudopanax crassifolius: functional significance of leaf morphology and anatomy. Ann Bot 71:61–70

    Google Scholar 

  • Gower ST, Vogt KA, Grier CC (1992) Carbon dynamics of rocky mountain Douglas-fir: influence of water and nutrient availability. Ecol Monogr 62:43–65

    Google Scholar 

  • Gower ST, Reich PB, Son Y (1993) Canopy dynamics and aboveground production of five tree species with different leaf longevities. Tree Physiol 12:327–345

    PubMed  Google Scholar 

  • Gower ST, Vogel J, Norman JM, Kucharik CJ, Steele SJ, Stow TK (1997) Carbon distribution and aboveground net primary production in aspen, jack pine and black spruce stands in Saskatchewan and Manitoba. J Geophys Res 102:29029–29041

    CAS  Google Scholar 

  • Gracia CA (1988) Chlorophyll content and leaf energetics of plant communities in south-eastern Queensland (Australia) in relation to water availability. In: di Castri F, C Floret, S Rambal, J Roy (eds) Time scales and water stress. Proceedings of the 5th International Conference on Mediterranean Ecosystems. International Union of Biological Sciences, Paris, pp 347–360

  • Grassi G, Bagnaresi U (2001) Foliar morphological and physiological plasticity in Picea abies and Abies alba saplings along a natural light gradient. Tree Physiol 21:959–967

    CAS  PubMed  Google Scholar 

  • Gratzer G, Darabant A, Chhetri PB, Rai PB, Eckmüllner O (2004) Interspecific variation in the response of growth, crown morphology, and survivorship to light of six tree species in the conifer belt of the Bhutan Himalayas. Can J For Res 34:1093–1107

    Google Scholar 

  • Greenway KJ, Macdonald SE, Lieffers VJ (1992) Is long-lived foliage in Picea mariana an adaptation to nutrient-poor conditions? Oecologia 91:184–191

    Google Scholar 

  • Greenwood MS (1995) Juvenility and maturation in conifers: current concepts. Tree Physiol 15:433–438

    PubMed  Google Scholar 

  • Greenwood MS, Day ME, Berlyn GP (2009) Regulation of foliar plasticity in conifers: developmental and environmental factors. J Sustain For 28:48–62

    Google Scholar 

  • Grier CC, Running SW (1977) Leaf area of mature northwestern coniferous forests: relation to site water balance. Ecology 58:893–899

    Google Scholar 

  • Grier CC, Elliott KJ, McCullough DG (1992) Biomass distribution and productivity of Pinus edulis–Juniperus monosperma woodlands of north-central Arizona. For Ecol Manag 50:331–350

    Google Scholar 

  • Groninger JW, Seiler JR, Peterson JA, Kreh RE (1996) Growth and photosynthetic responses of four Virginia Piedmont tree species to shade. Tree Physiol 16:773–778

    PubMed  Google Scholar 

  • Gutschick VP, Wiegel FW (1988) Optimizing the canopy photosynthetic rate by patterns of investment in specific leaf mass. Am Nat 132:67–86

    Google Scholar 

  • Hallik L, Kull O, Niinemets Ü, Aan A (2009a) Contrasting correlation networks between leaf structure, nitrogen and chlorophyll in herbaceous and woody canopies. Basic Appl Ecol 10:309–318

    CAS  Google Scholar 

  • Hallik L, Niinemets Ü, Wright IJ (2009b) Tolerance to shade and drought in relation to foliage structural and functional traits in temperate woody species. New Phytol 184:257–274

    Google Scholar 

  • Hansen U, Fiedler B, Rank B (2002) Variation of pigment composition and antioxidative systems along the canopy light gradient in a mixed beech/oak forest: a comparative study on deciduous tree species differing in shade tolerance. Trees Struct Funct 16:354–364

    CAS  Google Scholar 

  • Harcombe PA, Bill CJ, Fulton M, Glitzenstein JS, Marks PL, Elsik IS (2002) Stand dynamics over 18 years in a southern mixed hardwood forest, Texas, USA. J Ecol 90:947–957

    Google Scholar 

  • Harris JR, Bassuk NL (1993) Adaptation of trees to low light environments: effect on branching pattern of Fraxinus americana. J Arboric 19:339–343

    Google Scholar 

  • Hashimoto R (1991) Canopy development in young sugi (Cryptomeria japonica) stands in relation to changes with age in crown morphology and structure. Tree Physiol 8:129–143

    PubMed  Google Scholar 

  • Hay JA, Dellow UV (1952) New Zealand conifers: a note on their uses and importance. Tuatara 4:109–118

    Google Scholar 

  • Hemmerlein MT, Smith WK (1994) Structural scaling of light interception efficiency in Picea engelmannii and Abies lasiocarpa. Tree Physiol 14:1139–1148

    PubMed  Google Scholar 

  • Hessl AE, Milesi C, White MA, Peterson DL, Keane RE (2004) Ecophysiological parameters for Pacific Northwest trees. US Department of Agriculture, Forest Service, Pacific Northwest Research Station, Portland, OR

  • Hikosaka K, Hirose T (1997) Leaf angle as a strategy for light competition: optimal and evolutionary stable light extinction coefficient within a leaf canopy. Écoscience 4:501–507

    Google Scholar 

  • Hikosaka K, Terashima I (1995) A model of the acclimation of photosynthesis in the leaves of C3 plants to sun and shade with respect to nitrogen use. Plant Cell Environ 18:605–618

    CAS  Google Scholar 

  • Hikosaka K, Terashima I (1996) Nitrogen partitioning among photosynthetic components and its consequence in sun and shade plants. Funct Ecol 10:335–343

    Google Scholar 

  • Hirose T, Werger MJA (1995) Canopy structure and photon flux partitioning among species in a herbaceous plant community. Ecology 76:466–474

    Google Scholar 

  • Holder CD (2000) Geography of Pinus elliottii Engelm and Pinus palustris Mill. leaf life-spans in the southeastern USA. J Biogeogr 27:311–318

    Google Scholar 

  • Honda H, Fisher JB (1978) Tree branch angle: maximizing effective leaf area. Science 199:888–890

    CAS  PubMed  Google Scholar 

  • Horn HS (1971) The adaptive geometry of trees. Princeton University Press, Princeton

    Google Scholar 

  • Huang J, Wu Z, Guo SR (2007) Efects of low light intensity on photosynthetic capacity, photosynthetic nitrogen utilization efficiency and nitrogen partitioning in non-heading Chinese cabbage leaves. Acta Hortic 761:235–242

    CAS  Google Scholar 

  • Iio A, Fukasawa H, Nose Y, Kato S, Kakubari Y (2005) Vertical, horizontal and azimuthal variations in leaf photosynthetic characteristics within a Fagus crenata crown in relation to light acclimation. Tree Physiol 25:525–536

    Google Scholar 

  • Ishii H, Asano S (2009) The role of crown architecture, leaf phenology and photosynthetic activity in promoting complementary use of light among coexisting species in temperate forests. Ecol Res doi: 10.1007/s11284-009-0668-4

  • Iwasa Y, Cohen D, Leon JA (1984) Tree height and crown shape, as a result of competitive games. J Theor Biol 112:279–297

    Google Scholar 

  • Jack SB, Long JN (1992) Forest production and the organization of foliage within crowns and canopies. For Ecol Manag 49:233–245

    Google Scholar 

  • James SA, Bell DT (1996) Leaf orientation of juvenile Eucalyptus camaldulensis. Aust J Bot 44:139–156

    Google Scholar 

  • James SA, Bell DT (2000) Leaf orientation, light interception and stomatal conductance of Eucalyptus globulus ssp globulus leaves. Tree Physiol 20:815–823

    PubMed  Google Scholar 

  • Jarvis PG, Leverenz JW (1983) Productivity of temperate, deciduous and evergreen forests. In: Lange OL, Nobel PS, Osmond CB, Ziegler H (eds) Physiological plant ecology. Springer, Berlin, pp 233–280

    Google Scholar 

  • Jenkins JC, Chojnacky DC, Heath LS, Birdsey RA (2004) Comprehensive database of diameter-based biomass regressions for North American tree species. US Department of Agriculture Forest Service, Northeastern Research Station, Newtown Square

  • Kajimoto T, Matsuura Y, Osawa A, Abaimov AP, Zyryanova OA, Isaev AP, Yefremov DP, Mori S, Koike T (2006) Size–mass allometry and biomass allocation of two larch species growing on the continuous permafrost region in Siberia. For Ecol Manag 222:314–325

    Google Scholar 

  • Kawamura K (2009) A conceptual framework for the study of modular responses to local environmental heterogeneity within the plant crown and a review of related concepts and ideas. Ecol Res doi:10.1007/s11284-009-0688-0

  • Kayama M, Sasa K, Koike T (2002) Needle life span, photosynthetic rate and nutrient concentration of Picea glehnii, P jezoensis and P. abies planted on serpentine soil in northern Japan. Tree Physiol 22:707–716

    CAS  PubMed  Google Scholar 

  • Kempf JS, Pickett STA (1981) The role of branch length and angle in branching pattern of forest shrubs along a successional gradient. New Phytol 88:111–116

    Google Scholar 

  • Kennedy MC (2009) Functional–structural models optimize the placement of foliage units for multiple whole-canopy functions. Ecol Res doi:10.1007/s11284-009-0658-6

  • Kikuzawa K (2003) Phenological and morphological adaptations to the light environment in two woody and two herbaceous plant species. Funct Ecol 17:29–38

    Google Scholar 

  • King DA (2003) Allocation of above-ground growth is related to light in temperate deciduous saplings. Funct Ecol 17:482–488

    Google Scholar 

  • Kiniry JR (1998) Biomass accumulation and radiation use efficiency of honey mesquite and eastern red cedar. Biomass Bioenergy 15:467–473

    Google Scholar 

  • Kitajima K (1994) Relative importance of photosynthetic traits and allocation patterns as correlates of seedling shade tolerance of 13 tropical trees. Oecologia 98:419–428

    Google Scholar 

  • Kohyama T (1980) Growth pattern of Abies mariesii saplings under conditions of open-growth and suppression. Bot Mag Tokyo 93:13–24

    Google Scholar 

  • Kubota Y (2006) Spatial pattern and regeneration dynamics in a temperate Abies–Tsuga forest in southwestern Japan. J For Res 11:191–201

    Google Scholar 

  • Kull O, Aan A (1997) The relative share of graminoid and forb life-forms in a natural gradient of herb layer productivity. Ecography 20:146–154

    Google Scholar 

  • Kull O, Niinemets Ü (1993) Variation in leaf morphometry and nitrogen concentration in Betula pendula Roth., Corylus avellana L. and Lonicera xylosteum L. Tree Physiol 12:311–318

    PubMed  Google Scholar 

  • Kull O, Tulva I (2000) Modelling canopy growth and steady-state leaf area index in an aspen stand. Ann For Sci 57:611–621

    Google Scholar 

  • Kull O, Koppel A, Noormets A (1998) Seasonal changes in leaf nitrogen pools in two Salix species. Tree Physiol 18:45–51

    PubMed  Google Scholar 

  • Kull O, Broadmeadow M, Kruijt B, Meir P (1999) Light distribution and foliage structure in an oak canopy. Trees Struct Funct 14:55–64

    Google Scholar 

  • Küppers M (1994) Canopy gaps: competitive light interception and economic space filling—a matter of whole-plant allocation. In: Caldwell MM, Pearcy RW (eds) Exploitation of environmental heterogeneity by plants. Ecophysiological processes above- and belowground. Academic, San Diego, pp 111–144

    Google Scholar 

  • Lagergren A, Eklundh L, Grelle A, Lundblad M, Mölder M, Lankreijer H, Lindroth A (2004) Net primary production and light use efficiency in a mixed coniferous forest in Sweden. Plant Cell Environ 28:412–423

    Google Scholar 

  • Le Roux X, Gauthier H, Bégué A, Sinoquet H (1997) Radiation absorption and use by humid savanna grassland: assessment using remote sensing and modelling. Agric For Meteorol 85:117–132

    Google Scholar 

  • Lee DW, Richards JH (1991) Heteroblastic development in vines. In: Mooney HA, Putz FH (eds) The biology of vines. Cambridge University Press, New York, pp 205–243

    Google Scholar 

  • Leverenz JW (1992) Shade shoot structure and productivity of evergreen conifer stands. Scand J For Res 7:345–353

    Google Scholar 

  • Leverenz JW, Hinckley TM (1990) Shoot structure, leaf area index and productivity of evergreen conifer stands. Tree Physiol 6:135–149

    PubMed  Google Scholar 

  • Leverenz JW, Whitehead D, Stewart GH (2000) Quantitative analyses of shade-shoot architecture of conifers native to New Zealand. Trees Struct Funct 15:42–49

    Google Scholar 

  • Liang N, Nakadai T, Hirano T, Qu L, Koike T, Fujinuma Y, Inoue G (2004) In situ comparison of four approaches to estimating soil CO2 efflux in a northern larch (Larix kaempferi Sarg.) forest. Agric For Meteorol 123:97–117

    Google Scholar 

  • López-Serrano FR, Landete-Castillejos T, Martínez-Millán J, del Cerro-Barja A (2000) LAI estimation of natural pine forest using a non-standard sampling technique. Agric For Meteorol 101:95–111

    Google Scholar 

  • Lusk CH (2004) Leaf area and growth of juvenile temperate evergreens in low light: species of contrasting shade tolerance change rank during ontogeny. Funct Ecol 18:820–828

    Google Scholar 

  • Lusk CH, Contreras O (1999) Foliage area and crown nitrogen turnover in temperate rain forest juvenile trees of differing shade tolerance. J Ecol 87:973–983

    Google Scholar 

  • Lusk CH, Warton DI (2007) Global meta-analysis shows that relationships of leaf mass per area with species shade tolerance depend on leaf habit and ontogeny. New Phytol 176:764–774

    PubMed  Google Scholar 

  • Lusk CH, Falster DS, Jara-Vergara CK, Jimenez-Castillo M, Saldaña-Mendoza A (2008a) Ontogenetic variation in light requirements of juvenile rainforest evergreens. Funct Ecol 22:454–459

    Google Scholar 

  • Lusk CH, Reich PB, Montgomery RA, Ackerly DD, Cavender-Bares J (2008b) Why are evergreen leaves so contrary about shade? Trends Ecol Evol 23:299–303

    PubMed  Google Scholar 

  • Magnussen S, Smith VG, Yeatman CW (1986) Foliage and canopy characteristics in relation to aboveground dry matter increment of seven jack pine provenances. Can J For Res 16:464–470

    Google Scholar 

  • Marshall JD, Waring RH (1986) Comparison of methods of estimating leaf-area index in old-growth Douglas-fir. Ecology 67:975–979

    Google Scholar 

  • Mathieu F (2006) Évolution de la transpiration après coupe dans la sapinière à bouleau blanc, Forêt Montmorency, Québec. In: Maîtrise en sciences forestières. Université Laval, Laval. http://archimede.bibl.ulaval.ca/archimede/files/d6feadca-d29f-24a81-b27a-26d24cdada28dea/23817.html

  • McLeod SD, Running SW (1988) Comparing site quality indices and productivity in ponderosa pine stands of western Montana. Can J For Res 18:346–352

    Google Scholar 

  • McMillen GG, McClendon JH (1979) Leaf angle: an adaptive feature of sun and shade leaves. Bot Gaz 140:437–442

    Google Scholar 

  • Meir P, Kruijt B, Broadmeadow M, Barbosa E, Kull O, Carswell F, Nobre A, Jarvis PG (2002) Acclimation of photosynthetic capacity to irradiance in tree canopies in relation to leaf nitrogen concentration and leaf mass per unit area. Plant Cell Environ 25:343–357

    Google Scholar 

  • Mencuccini M, Grace J (1996) Hydraulic conductance, light interception and needle nutrient concentration in Scots pine stands and their relations with net primary productivity. Tree Physiol 16:459–468

    CAS  PubMed  Google Scholar 

  • Metcalfe DJ, Grubb PJ, Turner IM (1998) The ecology of very small-seeded shade-tolerant trees and shrubs in lowland rain forest in Singapore. Plant Ecol 134:131–149

    Google Scholar 

  • Miller PM, Eddleman LE, Miller JM (1995) Juniperus occidentalis juvenile foliage: advantages and disadvantages for a stress-tolerant, invasive conifer. Can J For Res 25:470–479

    Google Scholar 

  • Møller CM (1946) Untersuchungen über Laubmenge, Stoffverlust und Stoffproduktion des Waldes. Forstwiss Forsch 17:1–287

    Google Scholar 

  • Montague TG, Givnish TJ (1996) Distribution of black spruce versus eastern larch along peatland gradients: relationship to relative stature, growth rate, and shade tolerance. Can J Bot 74:1514–1532

    Google Scholar 

  • Mori A, Takeda H (2004) Functional relationships between crown morphology and within-crown characteristics of understory saplings of three codominant conifers in a subalpine forest in central Japan. Tree Physiol 24:661–670

    PubMed  Google Scholar 

  • Mori A, Mizumachi E, Sprugel DG (2008) Morphological acclimation to understory environments in Abies amabilis, a shade- and snow-tolerant conifer species of the Cascade Mountains, Washington, USA. Tree Physiol 28:815–824

    PubMed  Google Scholar 

  • Mugasha AG, Pluth DJ, Higginbotham KO, Takyi SK (1991) Foliar responses of black spruce to thinning and fertilization on a drained shallow peat. Can J For Res 21:152–163

    Google Scholar 

  • Myers BJ, Theiveyanathan S, O’Brien ND, Bond WJ (1996) Growth and water use of Eucalyptus grandis and Pinus radiata plantations irrigated with effluent. Tree Physiol 16:211–219

    PubMed  Google Scholar 

  • Nel EM, Wessman CA (1993) Canopy transmittance models for estimating forest leaf area index. Can J For Res 23:2579–2586

    Google Scholar 

  • Niinemets Ü (1996) Changes in foliage distribution with tree size and relative irradiance: differences between the saplings of Acer platanoides and Quercus robur. Ecol Res 11:269–281

    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 Struct Funct 11:144–154

    Google Scholar 

  • Niinemets Ü (1997b) Role of foliar nitrogen in light harvesting and shade tolerance of four temperate deciduous woody species. Funct Ecol 11:518–531

    Google Scholar 

  • Niinemets Ü (1998a) Adjustment of foliage structure and function to a canopy light gradient in two co-existing deciduous trees. Variability in leaf inclination angles in relation to petiole morphology. Trees Struct Funct 12:446–451

    Google Scholar 

  • Niinemets Ü (1998b) Growth of young trees of Acer platanoides and Quercus robur along a gap—understory continuum: interrelationships between allometry, biomass partitioning, nitrogen, and shade-tolerance. Int J Plant Sci 159:318–330

    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 (2004) Adaptive adjustments to light in foliage and whole-plant characteristics depend on relative age in the perennial herb Leontodon hispidus. New Phytol 162:683–696

    Google Scholar 

  • Niinemets Ü (2005) Key plant structural and allocation traits depend on relative age in the perennial herb Pimpinella saxifraga. Ann Bot 96:323–330

    PubMed  Google Scholar 

  • Niinemets Ü (2006) The controversy over traits conferring shade-tolerance in trees: ontogenetic changes revisited. J Ecol 94:464–470

    Google Scholar 

  • Niinemets Ü (2007) Photosynthesis and resource distribution through plant canopies. Plant Cell Environ 30:1052–1071

    CAS  PubMed  Google Scholar 

  • Niinemets Ü, Anten NPR (2009) Packing photosynthesis machinery: from leaf to canopy. In: Laisk A, Nedbal L, Govindjee (eds) Photosynthesis in silico: understanding complexity from molecules to ecosystems. Springer, Berlin, pp 363-399

  • Niinemets Ü, Kull O (1995a) 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, Kull O (1995b) Effects of light availability and tree size on the architecture of assimilative surface in the canopy of Picea abies: variation in shoot structure. Tree Physiol 15:791–798

    Google Scholar 

  • Niinemets Ü, Kull O (1998) Stoichiometry of foliar carbon constituents varies along light gradients in temperate woody canopies: implications for foliage morphological plasticity. Tree Physiol 18:467–479

    PubMed  Google Scholar 

  • Niinemets Ü, Lukjanova A (2003a) Needle longevity, shoot growth and branching frequency in relation to site fertility and within-canopy light conditions in Pinus sylvestris. Ann For Sci 60:195–208

    Google Scholar 

  • Niinemets Ü, Lukjanova A (2003b) Total foliar area and average leaf age may be more strongly associated with branching frequency than with leaf longevity in temperate conifers. New Phytol 158:75–89

    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

    Google Scholar 

  • Niinemets Ü, Bilger W, Kull O, Tenhunen JD (1998a) Acclimation to high irradiance in temperate deciduous trees in the field: changes in xanthophyll cycle pool size and in photosynthetic capacity along a canopy light gradient. Plant Cell Environ 21:1205–1218

    CAS  Google Scholar 

  • Niinemets Ü, Kull O, Tenhunen JD (1998b) An analysis of light effects on foliar morphology, physiology, and light interception in temperate deciduous woody species of contrasting shade tolerance. Tree Physiol 18:681–696

    PubMed  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

    PubMed  Google Scholar 

  • Niinemets Ü, Ellsworth DS, Lukjanova A, Tobias M (2001) Site fertility and the morphological and photosynthetic acclimation of Pinus sylvestris needles to light. Tree Physiol 21:1231–1244

    CAS  PubMed  Google Scholar 

  • Niinemets Ü, Cescatti A, Lukjanova A, Tobias M, Truus L (2002a) Modification of light-acclimation of Pinus sylvestris shoot architecture by site fertility. Agric For Meteorol 111:121–140

    Google Scholar 

  • Niinemets Ü, Ellsworth DS, Lukjanova A, Tobias M (2002b) Dependence of needle architecture and chemical composition on canopy light availability in three North American Pinus species with contrasting needle length. Tree Physiol 22:747–761

    PubMed  Google Scholar 

  • Niinemets Ü, Valladares F, Ceulemans R (2003) Leaf-level phenotypic variability and plasticity of invasive Rhododendron ponticum and non-invasive Ilex aquifolium co-occurring at two contrasting European sites. Plant Cell Environ 26:941–956

    PubMed  Google Scholar 

  • Niinemets Ü, Cescatti A, Christian R (2004) Constraints on light interception efficiency due to shoot architecture in broad-leaved Nothofagus species. Tree Physiol 24:617–630

    PubMed  Google Scholar 

  • Niinemets Ü, Cescatti A, Rodeghiero M, Tosens T (2005a) Leaf internal diffusion conductance limits photosynthesis more strongly in older leaves of Mediterranean evergreen broad-leaved species. Plant Cell Environ 28:1552–1566

    Google Scholar 

  • Niinemets Ü, Lukjanova A, Sparrrow AD, Turnbull MH (2005b) Light-acclimation of cladode photosynthetic potentials in Casuarina glauca: trade-offs between physiological and structural investments. Funct Plant Biol 32:571–582

    Google Scholar 

  • Niinemets Ü, Sparrow A, Cescatti A (2005c) Light capture efficiency decreases with increasing tree age and size in the southern hemisphere gymnosperm Agathis australis. Trees Struct Funct 19:177–190

    Google Scholar 

  • Niinemets Ü, Portsmuth A, Tobias M (2006a) Leaf size modifies support biomass distribution between stems, petioles and mid-ribs in temperate plants. New Phytol 171:91–104

    PubMed  Google Scholar 

  • Niinemets Ü, Tobias M, Cescatti A, Sparrrow AD (2006b) Size-dependent variation in shoot light-harvesting efficiency in shade-intolerant conifers. Int J Plant Sci 167:19–32

    Google Scholar 

  • Niklas KJ (1994) Plant allometry: the scaling of form and process. University of Chicago Press, Chicago

    Google Scholar 

  • Nilson T (1971) A theoretical analysis of the frequency of gaps in plant stands. Agric Meteorol 8:25–38

    Google Scholar 

  • Nock CA, Caspersen JP, Thomas SC (2008) Large ontogenetic declines in intra-crown leaf area index in two temperate deciduous tree species. Ecology 89:744–753

    CAS  PubMed  Google Scholar 

  • Norman JM, Campbell GS (1989) Canopy structure. In: Pearcy RW, Ehleringer JR, Mooney HA, Rundel PW (eds) Plant physiological ecology. Field methods and instrumentation. Chapman and Hall, London, pp 301–325

    Google Scholar 

  • O’Connell BM, Kelty MJ (1994) Crown architecture of understory and open-grown white pine (Pinus strobus L.) saplings. Tree Physiol 14:89–102

    PubMed  Google Scholar 

  • Oguchi R, Hikosaka K, Hirose T (2005) Leaf anatomy as a constraint for photosynthetic acclimation: differential responses in leaf anatomy to increasing growth irradiance among three deciduous trees. Plant Cell Environ 28:916–927

    Google Scholar 

  • Olff H (1992) Effects of light and nutrient availability on dry matter and N allocation in six successional grassland species. Testing for resource ratio effects. Oecologia 89:412–421

    Google Scholar 

  • Oren R, Waring RH, Stafford SG, Barrett JW (1987) Twenty-four years of ponderosa pine growth in relation to canopy leaf area and understory competition. For Sci 33:538–547

    Google Scholar 

  • Oren R, Phillips N, Ewers BE, Pataki DE, Megonigal JP (1999) Sap-flux-scaled transpiration responses to light, vapor pressure deficit, and leaf area reduction in a flooded Taxodium distichum forest. Tree Physiol 19:337–347

    PubMed  Google Scholar 

  • Osunkoya OO, Omar-Ali K, Amit N, Dayan J, Daud DS, Sheng TK (2007) Comparative height–crown allometry and mechanical design in 22 tree species of Kuala Belalong rainforest, Brunei, Borneo. Am J Bot 94:1951–1962

    Google Scholar 

  • Ovington JD (1957) Dry matter production by Pinus sylvestris L. Ann Bot 21:287–314

    Google Scholar 

  • Paquette A, Bouchard A, Cogliastro A (2007) Morphological plasticity in seedlings of three deciduous species under shelterwood under-planting management does not correspond to shade tolerance ranks. For Ecol Manag 241:278–287

    Google Scholar 

  • Parker GG, Davis MM, Chapotin SM (2002) Canopy light transmittance in Douglas-fir-western hemlock stands. Tree Physiol 22:147–157

    PubMed  Google Scholar 

  • Paz H (2003) Root/shoot allocation and root architecture in seedlings: variation among forest sites, microhabitats, and ecological groups. Biotropica 35:318–332

    Google Scholar 

  • Pearcy RW, Sims DA (1994) Photosynthetic acclimation to changing light environments: scaling from the leaf to the whole plant. In: Caldwell MM, Pearcy RW (eds) Exploitation of environmental heterogeneity by plants. Ecophysiological processes above- and belowground. Academic, San Diego, pp 145–174

    Google Scholar 

  • Pearcy RW, Valladares F, Wright SJ, Lasso de Paulis E (2004) A functional analysis of the crown architecture of tropical forest Psychotria species: do species vary in light capture efficiency and consequently in carbon gain and growth? Oecologia 139:163–177

    PubMed  Google Scholar 

  • Peichl M, Arain MA (2007) Allometry and partitioning of above- and belowground tree biomass in an age-sequence of white pine forests. For Ecol Manag 253:68–80

    Google Scholar 

  • Peterson DL, Spanner MA, Running SW, Teuber KB (1987) Relationship of thematic mapper simulator data to leaf area index of temperate coniferous forests. Remote Sens Environ 22:323–341

    Google Scholar 

  • Pickett STA, Kempf JS (1980) Branching patterns in forest shrubs and understory trees in relation to habitat. New Phytol 86:219–228

    Google Scholar 

  • Pierce LL, Running SW (1988) Rapid estimation of coniferous leaf area index using a portable integrating radiometer. Ecology 69:1762–1767

    Google Scholar 

  • Planchais I, Sinoquet H (1998) Foliage determinants of light interception in sunny and shaded branches of Fagus sylvatica L. Agric For Meteorol 89:241–253

    Google Scholar 

  • Pons TL (1976) An ecophysiological study in the field layer of ash coppice. I. Field measurements. Acta Bot Neerl 25:401–416

    Google Scholar 

  • Pons TL (1977) An ecophysiological study in the field layer of ash coppice. II. Experiments with Geum urbanum and Cirsium palustre in different light intensities. Acta Bot Neerl 26:29–42

    Google Scholar 

  • Poorter L, Werger MJA (1999) Light environment, sapling architecture, and leaf display in six rain forest tree species. Am J Bot 86:1464–1473

    PubMed  Google Scholar 

  • Poorter L, Bongers F, Sterck F, Wöl H (2000) Architecture of 53 rain forest tree species differing in adult stature and shade tolerance. Ecology 84(3):602–608

    Google Scholar 

  • Poorter L, Bongers L, Bongers F (2006) Architecture of 54 moist-forest tree species: traits, trade-offs, and functional groups. Ecology 87:1289–1301

    PubMed  Google Scholar 

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

    PubMed  Google Scholar 

  • Portsmuth A, Niinemets Ü (2007) Structural and physiological plasticity to light and nutrients in five temperate deciduous woody species of contrasting shade tolerance. Funct Ecol 21:61–77

    Google Scholar 

  • Prior LD, Eamus D, Bowman DMJS (2003) Leaf attributes in the seasonally dry tropics: a comparison of four habitats in northern Australia. Funct Ecol 17:504–515

    Google Scholar 

  • Pronk AA (2004) Irrigation and nitrogen use efficiency of Thuja occidentalis grown on sandy soils. In: de Wit (CT) Graduate school for production ecology and resource conservation. Wageningen University, Wageningen

  • Pronk TE, Schieving F, Anten NPR, Werger MJA (2007) Plants that differ in height investment can coexist if they are distributing non-uniformly within an area. Ecol Complex 4:182–191

    Google Scholar 

  • Quero JL, Villar R, Marañon T, Zamora R, Poorter L (2007) Seed-mass effects in four Mediterranean Quercus species (Fagaceae) growing in contrasting light environments. Am J Bot 94:1795–1803

    Google Scholar 

  • Rambal S (2001) Productivity of Mediterranean-type ecosystems. In: Mooney HA, Saugier B, Roy J (eds) Terrestrial global productivity: past present and future. Academic, San Diego, pp 315–344

    Google Scholar 

  • Reich PB, Walters MB, Ellsworth DS (1992) Leaf life-span in relation to leaf, plant, and stand characteristics among diverse ecosystems. Ecol Monogr 62:365–392

    Google Scholar 

  • Reich PB, Tjoelker MG, Walters MB, Vanderklein DW, Buschena C (1998) Close association of RGR, leaf and root morphology, seed mass and shade tolerance in seedlings of nine boreal tree species grown in high and low light. Funct Ecol 12:327–338

    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 

  • Richardson AD, Ashton PMS, Berlyn GP, McGroddy ME, Cameron IR (2001) Within-crown foliar plasticity of western hemlock, Tsuga heterophylla, in relation to stand age. Ann Bot 88:1007–1015

    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

    Google Scholar 

  • Rikhari HC, Palni LMS, Sharma S, Nandi SK (1998) Himalayan yew: stand structure, canopy damage, regeneration and conservation strategy. Environ Conserv 25:334–341

    Google Scholar 

  • Ross J (1981) The radiation regime and architecture of plant stands. Junk, The Hague

  • Rousseaux MC, Hall AJ, Sanchez RA (2000) Basal leaf senescence in a sunflower (Helianthus annuus) canopy: responses to increased R/FR ratio. Physiol Plant 110:477–482

    CAS  Google Scholar 

  • Runyon J, Waring RH, Goward SN, Welles JM (1994) Environmental limits on net primary production and light-use efficiency across the Oregon transect. Ecol Appl 4:226–237

    Google Scholar 

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

    Google Scholar 

  • Ryan MG, Binkley D, Fownes JH, Giardina CP, Senock RS (2004) An experimental test of the causes of forest growth decline with stand age. Ecol Monogr 74:393–414

    Google Scholar 

  • Ryel RJ, Beyschlag W (1995) Benefits associated with steep foliage orientation in two tussock grasses of the American Intermountain West. A look at water-use-efficiency and photoinhibition. Flora 190:251–260

    Google Scholar 

  • Saito S, Sato T, Kominami Y, Nagamatsu D, Kuramoto S, Sakai T, Tabuchi R, Sakai A (2004) Modeling the vertical foliage distribution of an individual Castanopsis cuspidata (Thunb.) Schottky, a dominant broad-leaved tree in Japanese warm-temperate forest. Trees Struct Funct 18:486–491

    Google Scholar 

  • Sampson DA, Allen HL (1995) Direct and indirect estimates of leaf area index (LAI) for lodgepole and loblolly pine stands. Trees Struct Funct 9:119–122

    Google Scholar 

  • Sánchez-Gómez D, Valladares F, Zavala MA (2006) Functional traits and plasticity underlying shade tolerance in seedlings of four Iberian forest tree species. Tree Physiol 26:1425–1433

    PubMed  Google Scholar 

  • Satoo T (1974) Primary production relations of a young stand of Metasequoia glyptostroboides planted in Tokyo: materials for the studies of growth in forest stands. 13. Bull Tokyo Univ For 66:153–164

    Google Scholar 

  • Schulze ED (1982) Plant life forms and their carbon, water and nutrient relations. In: Lange OL, Nobel PS, Osmond CB, Ziegler H (eds) Physiological plant ecology. Springer, Berlin, pp 616–676

    Google Scholar 

  • Schulze ED, Fuchs M, Fuchs MI (1977) Spacial distribution of photosynthetic capacity and performance in a mountain spruce forest of northern Germany. III. The significance of the evergreen habit. Oecologia 30:239–248

    Google Scholar 

  • Scurlock JMO, Asner GP, Gower ST (2001) Worldwide historical estimates of leaf area index, 1932–2000. Oak Ridge National Laboratory, Oak Ridge, TN

    Google Scholar 

  • Selaya NG, Anten NPR, Ooomen RJ, Matthies M, Werger MJA (2007) Above-ground biomass investments and light interception of tropical forest trees and lianas early in succession. Ann Bot 99:141–151

    CAS  PubMed  Google Scholar 

  • Selaya NG, Ooomen RJ, Netten JJC, Werger MJA, Anten NPR (2008) Biomass allocation and leaf life span in relation to light interception by tropical forest plants during the first years of secondary succession. J Ecol 96:1211–1221

    Google Scholar 

  • Sellin A (2000) Estimating needle area from geometric measurements: application of different calculation methods to Norway spruce. Trees Struct Funct 14:215–222

    Google Scholar 

  • Sheil D, Salim A, Chave J, Vanclay J, Hawthorne WD (2006) Illumination–size relationships of 109 coexisting tropical forest tree species. J Ecol 94:494–507

    Google Scholar 

  • Shibuya M, Hasaba H, Yajima T, Takahashi K (2005) Effect of thinning on allometry and needle-age distribution of trees in natural Abies stands of northern Japan. J For Res 10:15–20

    Google Scholar 

  • Smith T, Huston M (1989) A theory of the spatial and temporal dynamics of plant communities. Vegetatio 83:49–69

    Google Scholar 

  • Smolander H, Stenberg P, Linder S (1994) Dependence of light interception efficiency of Scots pine shoots on structural parameters. Tree Physiol 14:971–980

    PubMed  Google Scholar 

  • Sprugel DG, Brooks JR, Hinckley TM (1996) Effects of light on shoot geometry and needle morphology in Abies amabilis. Tree Physiol 16:91–98

    PubMed  Google Scholar 

  • Steingraeber DA, Kascht LJ, Frank DH (1979) Variation of shoot morphology and bifurcation ratio in sugar maple (Acer saccharum) saplings. Am J Bot 66:441–445

    Google Scholar 

  • Stenberg P, Linder S, Smolander H, Flower-Ellis J (1994) Performance of the LAI-2000 plant canopy analyzer in estimating leaf area index of some Scots pine stands. Tree Physiol 14:981–995

    PubMed  Google Scholar 

  • Stenberg P, Smolander H, Sprugel DG, Smolander S (1998) Shoot structure, light interception, and distribution of nitrogen in an Abies amabilis canopy. Tree Physiol 18:759–767

    PubMed  Google Scholar 

  • Stenberg P, Kangas T, Smolander H, Linder S (1999) Shoot structure, canopy openness, and light interception in Norway spruce. Plant Cell Environ 22:1133–1142

    Google Scholar 

  • Stenberg P, Palmroth S, Bond BJ, Sprugel DG, Smolander H (2001) Shoot structure and photosynthetic efficiency along the light gradient in a Scots pine canopy. Tree Physiol 21:805–814

    CAS  PubMed  Google Scholar 

  • Stephens GR, Ward JS (1992) Sixty years of natural change in unmanaged mixed hardwood forests. Connecticut Agricultural Experiment Station, New Haven, Bull 902

    Google Scholar 

  • Sterck FJ, Bongers F (2001) Crown development in tropical rain forest trees: patterns with tree height and light availability. J Ecol 89:1–13

    Google Scholar 

  • Sterck FJ, Schieving F (2007) 3-D growth patterns of trees: effects of carbon economy, meristem activity, and selection. Ecol Monogr 77:405–420

    Google Scholar 

  • Sumida A, Komiyama A (1997) Crown spread patterns for five deciduous broad-leaved woody species: ecological significance of the retention patterns of larger branches. Ann Bot 80:759–766

    Google Scholar 

  • Tadaki Y (1966) Some discussions on the leaf biomass of forest stands and trees. Bull Gov For Exp Stn 184:135–161

    Google Scholar 

  • Tadaki Y (1991) Productivity of coniferous forests in Japan. In: Nakagoshi N, Golley FB (eds) Coniferous forest ecology, from an international perspective. Symposium held at the International Congress of Ecology, Yokohama, Japan, 1990. SPB, The Hague, pp 109–119

    Google Scholar 

  • Tadaki Y, Kawasaki Y (1966) Studies on the production structure of forest. IX. Primary productivity of a young Cryptomeria plantation with excessively high stand density. J Jpn For Soc 48:55–61

    Google Scholar 

  • Tadaki Y, Ogata N, Nagatomo Y (1965) The dry matter productivity in several stands of Cryptomeria japonica in Kyushu. Bull Gov For Exp Stn Tokyo 173:45–66

    Google Scholar 

  • Tadaki Y, Ogata N, Nagatomo Y, Yoshida T (1966) Studies on the production structure of forest. X. Primary productivity of an unthinned 45-year old stand of Chamaecyparis obtusa. J Jpn For Soc 48:387–393

    Google Scholar 

  • Tadaki Y, Ogata N, Nagatomo Y (1967) Studies on the production structure of forest. XI. Primary productivities of 28-year old plantations of Cryptomeria of cuttings and seedlings origin. Bull Gov For Exp Stn Tokyo 199:47–65

    Google Scholar 

  • Tadaki Y, Itatiya K, Tochiaki K, Miyauchi H, Matsuda U (1970) Studies on the production of structure of forest. XVI. Primary productivity of Abies veitchii forests in subalpine zone of Mt. Fuji. Bull Gov For Exp Stn Tokyo 229:1–22

    Google Scholar 

  • Takahashi K, Lechowicz MJ (2008) Do interspecific differences in sapling growth traits contribute to the co-dominance of Acer saccharum and Fagus grandifolia? Ann Bot 101:103–109

    PubMed  Google Scholar 

  • Takahashi K, Seino T, Kohyama T (2005) Plastic changes of leaf mass per area and leaf nitrogen content in response to canopy openings in saplings of eight deciduous broad-leaved tree species. Ecol Res 20:17–23

    CAS  Google Scholar 

  • Terashima I, Miyazawa S-I, Hanba YT (2001) Why are sun leaves thicker than shade leaves?—Consideration based on analyses of CO2 diffusion in the leaf. J Plant Res 114:93–105

    CAS  Google Scholar 

  • Terashima I, Hanba YT, Tazoe Y, Vyas P, Yano S (2006) Irradiance and phenotype: comparative eco-development of sun and shade leaves in relation to photosynthetic CO2 diffusion. J Exp Bot 57:343–354

    CAS  PubMed  Google Scholar 

  • Thomas SC, Winner WE (2000) A rotated ellipsoidal angle density function improves estimation of foliage inclination distributions in forest canopies. Agric For Meteorol 100:19–24

    Google Scholar 

  • Toledo-Aceves T, Swaine MD (2008) Biomass allocation and photosynthetic responses of lianas and pioneer tree seedlings to light. Acta Oecol 34:38–49

    Google Scholar 

  • Torquebiau EF (1988) Photosynthetically active radiation environment, patch dynamics and architecture in a tropical rainforest in Sumatra. Aust J Plant Physiol 15:327–342

    Google Scholar 

  • Utsugi H (1999) Angle distribution of foliage in individual Chamaecyparis obtusa canopies and effect of angle on diffuse light penetration. Trees Struct Funct 14:1–9

    Google Scholar 

  • Utsugi H, Araki M, Kawasaki T, Ishizuka M (2006) Vertical distributions of leaf area and inclination angle, and their relationship in a 46-year-old Chamaecyparis obtusa stand. For Ecol Manag 225:104–112

    Google Scholar 

  • Valladares F, Niinemets Ü (2007) The architecture of plant crowns: from design rules to light capture and performance. In: Pugnaire FI, Valladares F (eds) Handbook of functional plant ecology. CRC, Boca Raton, pp 101–149

    Google Scholar 

  • Valladares F, Niinemets Ü (2008) Shade tolerance, a key plant feature of complex nature and consequences. Annu Rev Ecol Evol Syst 39:237–257

    Google Scholar 

  • Valladares F, Chico JM, Aranda I, Balaguer L, Dizengremel P, Manrique E, Dreyer E (2002) The greater seedling high-light tolerance of Quercus robur over Fagus sylvatica is linked to a greater physiological plasticity. Trees Struct Funct 16:395–403

    CAS  Google Scholar 

  • Vanninen P, Ylitalo H, Sievänen R, Mäkelä A (1996) Effects of age and site quality on the distribution of biomass in Scots pine (Pinus sylvestris L.). Trees Struct Funct 10:231–238

    Google Scholar 

  • Veres JS, Pickett STA (1982) Branching patterns of Lindera benzoin beneath gaps and closed canopies. New Phytol 91:767–772

    Google Scholar 

  • Vertessy RA, Watson FGR, O’Sullivan SK (2001) Factors determining relations between stand age and catchment water balance in mountain ash forests. For Ecol Manag 143:13–26

    Google Scholar 

  • Vogel JG, Gower ST (1998) Carbon and nitrogen dynamics of boreal jack pine stands with and without a green alder understory. Ecosystems 1:386–400

    CAS  Google Scholar 

  • Vose JM, Swank WT (1990) Assessing seasonal leaf area dynamics and vertical leaf area distribution in eastern white pine (Pinus strobus L.) with a portable light meter. Tree Physiol 7:125–134

    PubMed  Google Scholar 

  • Walters MB, Reich PB (1999) Research review. Low-light carbon balance and shade tolerance in the seedlings of woody plants: do winter deciduous and broad-leaved evergreen species differ? New Phytol 143:143–154

    Google Scholar 

  • Walters MB, Kruger EL, Reich PB (1993) Growth, biomass distribution and CO2 exchange of northern hardwood seedlings in high and low light: relationships with successional status and shade tolerance. Oecologia 94:7–16

    Google Scholar 

  • Wang W-M, Li Z-L, Su H-B (2007) Comparison of leaf angle distribution functions: effects on extinction coefficient and fraction of sunlit foliage. Agric For Meteorol 143:106–122

    Google Scholar 

  • Ward JS, Stephens GR (1993) Influence of crown class and shade tolerance on individual tree development during deciduous forest succession in Connecticut, USA. For Ecol Manag 60:207–236

    Google Scholar 

  • Werger MJA, Hirose T (1988) Effects of light climate and nitrogen partitioning on the canopy structure of stands of a dicotyledonous, herbaceous vegetation. In: Werger MJA, van der Aart PJM, During HJ, Verhoeven JTA (eds) Plant form and vegetation structure adaptation plasticity and relation to herbivory. SPB, The Hague, pp 171–181

    Google Scholar 

  • Whitney GG (1976) The bifurcation ratio as an indicator of adaptive strategy in woody plant species. Bull Torrey Bot Club 103:67–72

    Google Scholar 

  • Whittaker RH (1966) Forest dimensions and production in the Great Smoky Mountains. Ecology 44:103–121

    Google Scholar 

  • Witkowski ETF, Lamont BB (1991) Leaf specific mass confounds leaf density and thickness. Oecologia 88:486–493

    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

    CAS  PubMed  Google Scholar 

  • Xu M, Harrington TB (1998) Foliage biomass distribution of loblolly pine as affected by tree dominance, crown size, and stand characteristics. Can J For Res 28:887–892

    Google Scholar 

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Acknowledgments

The author’s work on light harvesting, plant structure and environmental controls has been funded by the Estonian Ministry of Education and Science (Grant SF1090065s07) and the Estonian Science Foundation.

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  1. Institute of Agricultural and Environmental Sciences, Estonian University of Life Sciences, Kreutzwaldi 1, 51014, Tartu, Estonia

    Ülo Niinemets

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Correspondence to Ülo Niinemets.

Appendix

Appendix

See Table 1.

Table 1 Estimates of stand projected leaf area index in essentially mono-specific stands (L) and average leaf life-span (Λav) for 41 temperate conifer species
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Niinemets, Ü. A review of light interception in plant stands from leaf to canopy in different plant functional types and in species with varying shade tolerance. Ecol Res 25, 693–714 (2010). https://doi.org/10.1007/s11284-010-0712-4

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