Skip to main content

Light Heterogeneity and Plants: from Ecophysiology to Species Coexistence and Biodiversity

  • Chapter
Progress in Botany

Part of the book series: Progress in Botany ((BOTANY,volume 64))

Abstract

Light is produced by changes in the energy level of electrons (when an electron changes from a high-energy, Or excited, State to a low-energy state, Its atom will emit a photon), but its dual nature makes it scientifically puzzling: it moves through space as a wave, but when it encounters matter it behaves like a particle, The quantum (Achenbach 2001). In practice “light” is used for the portion of the electromagnetic spectrum in the vicinity of visible light. In plant biology and ecology, photosynthetically active radiation (PAR), Which essentially coincides with visible light, Is probably the most relevant measure of light. The PAR region is where energy is most abundant (it represents on average 43% of the solar irradiance), And it is strong enough to drive electron transport in photosynthesis, Yet weak enough to avoid excessive damage to biological molecules. However, There exists no worldwide network for PAR measurements like the network of actinometric stations, Where global, Direct, diffuse and reflected solar radiation are measured using unified instruments and methodology and are metrologically based on the world radiometric reference (Ross and Sulev 2000). The dual nature of light, I.e., particle versus wave, Affects the way light in general and PAR in particular is measured. One group of sensors measures energy (e.g., W m−2), The other group quanta (e.g., μmol m−2 s−1).

This is a preview of subscription content, log in via an institution to check access.

Access this chapter

Chapter
USD 29.95
Price excludes VAT (USA)
  • Available as PDF
  • Read on any device
  • Instant download
  • Own it forever
eBook
USD 259.00
Price excludes VAT (USA)
  • Available as PDF
  • Read on any device
  • Instant download
  • Own it forever
Softcover Book
USD 329.99
Price excludes VAT (USA)
  • Compact, lightweight edition
  • Dispatched in 3 to 5 business days
  • Free shipping worldwide - see info
Hardcover Book
USD 329.99
Price excludes VAT (USA)
  • Durable hardcover edition
  • Dispatched in 3 to 5 business days
  • Free shipping worldwide - see info

Tax calculation will be finalised at checkout

Purchases are for personal use only

Institutional subscriptions

Preview

Unable to display preview. Download preview PDF.

Unable to display preview. Download preview PDF.

References

  • Abrams MD, Mostoller SA (1995) Gas exchange, Leaf structure and nitrogen in contrasting successional tree species growing in open and understory sites during a drought. Tree Physiol 15:361–370

    PubMed  Google Scholar 

  • Abrams MD, Kloeppel BD, Kubiske ME (1992) Ecophysiological and morphological responses to shade and drought in two contrasting ecotypes of Prunus serotina. Tree Physiol 10:343–355

    PubMed  Google Scholar 

  • Achenbach J (2001) The power of light. Natl Geogr 200:2–31

    Google Scholar 

  • Ackerly DD (2000) Taxon sampling, correlated evolution, And independent contrasts. Evolution 54:1480–1492

    PubMed  CAS  Google Scholar 

  • Ackerly DD, Dudley SA, Sultan SE, Schmitt J, Coleman JS, Randal Linder C, Sandquist DR, Geber MA, Evans AS, Dawson TE, Lechowicz MJ (2000) The evolution of plant ecophysiological traits: recent advances and future directions. Bioscience 50:979–995

    Google Scholar 

  • Adler I, Barabe D, Jean V (1997) A history of the study of phyllotaxis. Ann Bot 80:231–244

    Google Scholar 

  • Agyeman VK, Swaine MD, Thompson J (1999) Responses of tropical forest tree seedlings to irradiance and the derivation of a light response index. J Ecol 87:815–827

    Google Scholar 

  • Aiba S, Kohyama T (1997) Crown architecture and life-history traits of 14 tree species in a warm-temperate rain forest: significance of spatial heterogeneity. J Ecol 85:611–624

    Google Scholar 

  • Aphalo PJ, Ballare CL, Scopel AL (1999) Plant-plant signalling, The shade-avoidance response and competition. J Exp Bot 50:1629–1634

    CAS  Google Scholar 

  • Arntz AM, Delph LF (2001) Patterns and process: evidence for the evolution of photosynthetic traits in natural populations. Oecologia 127:455–467

    Google Scholar 

  • Arntz AM, DeLucia EH, Jordan N (2000) From fluorescence to fitness: variation in photosynthetic rate affects fecundity and survivorship. Ecology 81:2567–2576

    Google Scholar 

  • Bainbrige R, Evans GC, Rackham O (1966) Light as an ecological factor. Blackwell Scientific, London

    Google Scholar 

  • Balaguer L, Martínez-Ferri E, Valladares F, Pérez-Corona ME, Baquedano FJ, Castillo FJ, Manrique E (2001) Population divergence in the plasticity of the response of Quercus coccifera to the light environment. Funct Ecol 15:124–135

    Google Scholar 

  • Baldocchi D, Collineau S (1994) The physical nature of solar radiation in heterogeneous canopies: spatial and temporal attributes. In: Caldwell MM, Pearcy RW (eds) Exploitation of environmental heterogeneity by plants. Academic Press, San Diego, pp 21–71

    Google Scholar 

  • Ballare CL (1999) Keeping up with the neighbours: phytochrome sensing and other signalling mechanisms. Trends Plant Sci 4:97–102

    PubMed  Google Scholar 

  • Barnes BB, Zak DR, Denton SR, Spurr SH (1998) Forest ecology. Wiley, New York

    Google Scholar 

  • Baruch Z, Pattison RR, Goldstein G (2000) Responses to light and water availability of four invasive Melastomataceae in the Hawaiian Islands. Int J Plant Sci 161:107–118

    PubMed  Google Scholar 

  • Bascompte J, Rodriguez MA (2001) Habitat patchiness and plant species richness. Ecol Lett 4:1–4

    Google Scholar 

  • Battaglia M, Cherry ML, Beadle CL, Sands PJ, Hingston A (1998) Prediction of leaf area index in eucalypt plantations: effects of water stress and temperature. Tree Physiol 18:521–528

    PubMed  Google Scholar 

  • Bazzaz FA (1979) The physiological ecology of plant succession. Annu Rev Ecol Syst 10:351–371

    Google Scholar 

  • Bazzaz FA (1991) Habitat selection in plants. Am Nat 137: S116–S130

    Google Scholar 

  • Bazzaz FA (1996) Plants in changing environments: linking physiological, population, and community ecology. Cambridge University Press, Cambridge

    Google Scholar 

  • Bazzaz FA, Stinson KA (1999) Genetic vs. environmental control of ecophysiological processes: some challenges for predicting community responses to global change. In: Press MC, Scholes JD, Barker MG (eds) Physiological plant ecology. Blackwell Science, Cornwall, pp 283–296

    Google Scholar 

  • Becker P, Smith AP (1990) Spatial autocorrelation of solar radiation in a tropical moist forest understory. Agric For Meteorol 52:373–379

    Google Scholar 

  • Bell AD (1984) Dynamic morphology: a contribution to plant population ecology. In: Dirzo R, Sarukhán J (eds) Perspectives on plant population ecology. Sinauer, Sunderland, MA, pp 48–65

    Google Scholar 

  • Bell AD (1993) Plant form. Oxford University Press, New York

    Google Scholar 

  • Beyschlag W, Ryel RJ (1999) Canopy photosynthesis modeling. In: Pugnaire FI, Valladares F (eds) Handbook of functional plant ecology. Marcel Dekker, New York, pp 771–804

    Google Scholar 

  • Björkman O (1981) Responses to different quantum flux densities. In: Lange OL, Nobel PS, Osmond CB, Ziegler H (eds) Physiological plant ecology. Springer, Berlin Heidelberg New York, pp 57–107

    Google Scholar 

  • Bongers F, Popma J (1990) Leaf characteristics of the tropical rain forest flora of Los-Tuxtlas, Mexico. Bot Gaz 151:354–365

    Google Scholar 

  • Bossard CC, Rejmanek M (1992) Why have green stems? Funct Ecol 6:197–205

    Google Scholar 

  • Bradshaw AD (1965) Evolutionary significance of phenotypic plasticity in plants. Adv Genet 13:115–155

    Google Scholar 

  • Braithwaite R (1996) Biodiversity and fire in the savanna landscape. In: Solbrig DT, Medina E, Silva JF (eds) Biodiversity and savanna ecosystem processes. Springer, Berlin Heidelberg New York, pp 121–140

    Google Scholar 

  • Bungard RA, Ruban AV, Hibberd JM, Press MC, Horton P, Scholes JD (1999) Unusual carotenoid composition and a new type of xanthophyll cycle in plants. Proc Natl Acad Sei USA 96:1135–1139

    CAS  Google Scholar 

  • Callaway RM, Pugnaire FI (1999) Facilitation in plant communities. In: Pugnaire FI, Valladares F (eds) Handbook of functional plant ecology. Marcel Dekker, New York, pp 623–648

    Google Scholar 

  • Canadell J, Roda F (1991) Root biomass of Quercus ilex in a montane Mediterranean forest. Can J For Res 21:1771–1778

    Google Scholar 

  • Canham CD, Denslow JS, Platt WJ, Runkle JR, Spies TA, White PS (1990) Light regimes beneath closed canopies and tree-fall gaps in temperate and tropical forests. Can J For Res 20:620–631

    Google Scholar 

  • Chazdon RL (1988) Sunflecks and their importance to forest understory plants. Adv Ecol Res 18:1–63

    Google Scholar 

  • Chazdon RL (1992) Photosynthetic plasticity of two rain forest shrubs across natural gap transects. Oecologia 92:586–595

    Google Scholar 

  • Chazdon RL, Williams K, Field CB (1988) Interactions between crown structure and light environment in five rain forest Piper species. Am J Bot 75:1459–1471

    Google Scholar 

  • Christensen NL (1997) Managing for heterogeneity and complexity on dynamic landscapes. In: Pickett STA, Ostfeld RS, Shachak M, Likens GE (eds) The ecological basis of conservation heterogeneity, Ecosystems and biodiversity. Chapman and Hall, New York, pp 167–186

    Google Scholar 

  • Cipollini DF, Schultz JC (1999) Exploring costs constraints on stem elongation in plants using phenotypic manipulation. Am Nat 153:236–242

    Google Scholar 

  • Clark DA, Clark DB (2001) Getting to the canopy: tree height growth in a neotropical rain forest. Ecology 82:1460–1472

    Google Scholar 

  • Comstock JP, Ehleringer JR (1988) Contrasting photosynthetic behavior in leaves and twigs of Hymenoclea salsola, green-twigged warm desert shrub. Am J Bot 75:1360–1370

    Google Scholar 

  • Day TA (1993) Relating Uv-B radiation screening effectiveness of foliage to absorbing-compound concentration and anatomical characteristics in a diverse group of plants. Oecologia 95:542–550

    Google Scholar 

  • Day TA, Vogelmann TC, Delucia EH (1992) Are some plant life forms more effective than others in screening out ultraviolet-B radiation? Oecologia 92:513–519

    Google Scholar 

  • De Jong G, Gavrilets S (2000) Maintenance of genetic variation in phenotypic plasticity: the role of environmental variation. Genet Res 76:295–304

    PubMed  Google Scholar 

  • Demmig-Adams B, Adams WW (2000) Photosynthesis — harvesting sunlight safely. Nature 403:371–374

    PubMed  CAS  Google Scholar 

  • DePuit EJ, Caldwell MM (1975) Stem and leaf gas exchange of two arid land shrubs. Am J Bot 62:954–961

    Google Scholar 

  • De Reffye P, Houllier F (1997) Modelling plant growth and architecture: some recent advances and applications to agronomy and forestry. Curr Sci (Bangalore) 73:984–992

    Google Scholar 

  • Deutschman DH, Levin SA, Pacala SW (1999) Error propagation in a forest succession model: the role of fine-scale heterogeneity in light. Ecology 80:1927–1943

    Google Scholar 

  • DeWitt TJ, Sih A, Wilson DS (1998) Costs and limits of phenotypic plasticity. Trends Ecol Evol 13:77–81

    PubMed  CAS  Google Scholar 

  • Dudley SA, Schmitt J (1996) Testing the adaptive plasticity hypothesis: density-dependent selection on manipulated stem length in Impatiens capensis. Am Nat 147:445–465

    Google Scholar 

  • Durand LZ, Goldstein G (2001) Photosynthesis, photoinhibition, And nitrogen use efficiency in native and invasive tree ferns in Hawaii. Oecologia 126:345–354

    Google Scholar 

  • Ehleringer JR, Cooper TA (1992) On the role of orientation in reducing photoinhibitory damage in photosynthetic-twig desert shrubs. Plant Cell Environ 15:301–306

    Google Scholar 

  • Ehleringer JR, Forseth IN (1989) Diurnal leaf movements and productivity in canopies. In: Russell G, Marshall B, Jarvis PG (eds) Plant canopies: their growth, Form and function. Cambridge University Press, Cambridge, pp 129–142

    Google Scholar 

  • Ehleringer JR, Werk KS (1986) Modifications of solar-radiation absorption patterns and implications for carbon gain at the leaf level. In: Givnish TJ (eds) On the economy of plant form and function. Cambridge University Press, Cambridge, pp 564–571

    Google Scholar 

  • Endler JA (1993) The color of light in forests and its implications. Ecol Monogr 61:1–27

    Google Scholar 

  • Englund SR, O’Brien JJ, Clark DB (2000) Evaluation of digital and film hemispherical photography and spherical densiometry for measuring forest light environments. Can J For Res 30:1999–2005

    Google Scholar 

  • Evans JR, von Caemmerer S, Adams WW III (1988) Ecology of photosynthesis in sun and shade. CSIRO, Melbourne

    Google Scholar 

  • Faria T, Silvério D, Breia E, Cabrai R, Abadía A, Abadía J, Pereira JS, Chaves MM (1998) Differences in the response of carbon assimilation to summer stress (water deficits, high light and temperature) in four Mediterranean tree species. Physiol Planta 102:419–428

    CAS  Google Scholar 

  • Farquhar GD, von Caemmerer S, Berry JA (2001) Models of photosynthesis. Plant Physiol 125:42–45

    PubMed  CAS  Google Scholar 

  • Filella I, Penuelas J (1998) Visible and near-infrared reflectance techniques for diagnosing plant physiological status. Trends Plant Sci 3:151–156

    Google Scholar 

  • Gamon JA, Qiu H (1999) Ecological applications of remote sensing at multiple scales. In: Pugnaire FI, Valladares F (eds) Handbook of functional plant ecology. Marcel Dekker, New York, pp 805–846

    Google Scholar 

  • Gautier H, Mech R, Prusinkiewicz P, Varlet-Grancher C (2000) 3D architectural modelling of aerial photomorphogenesis in white clover (Trifolium repens L.) using L-systems. Ann Bot 85:359–370

    Google Scholar 

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

    Google Scholar 

  • Grammatikopoulos G, Kyparissis A, Drilias P, Petropoulou Y, Manetas Y (1998) Effects of UV-B radiation on cuticle thickness and nutritional value of leaves in two Mediterranean evergreen sclerophylls. J Plant Physiol 153:506–512

    CAS  Google Scholar 

  • Grime JP, Crick JC, Rincon E (1986) The ecological significance of plasticity. In: Jennings DH, Trewavas AJ (eds) Plasticity in plants. Company of Biologists, Cambridge, pp 5–29

    Google Scholar 

  • Haase P, Pugnaire FI, Clark SC, Incoll LD (1999) Diurnal and seasonal changes in cladode photosynthetic rate in relation to canopy age structure in the leguminous shrub Retama sphaerocarpa. Funct Ecol 13:640–649

    Google Scholar 

  • Han BP, Virtanen M, Koponen J, Straskraba M (2000) Effect of photoinhibition on algal photosynthesis: a dynamic model. J Plankton Res 22:865–885

    CAS  Google Scholar 

  • Hanski I (1997) Habitat destruction and metapopulation dynamics. In: Pickett STA, Ostfeld RS, Shachak M, Likens GE (eds) The ecological basis of conservation heterogeneity, ecosystems and biodiversity. Chapman and Hall, New York, pp 217–227

    Google Scholar 

  • Hanski I, Gilpin ME (1997) Metapopulation biology: ecology, Genetics, And evolution. Academic Press, San Diego

    Google Scholar 

  • Hari P, Nikinmaa E, Korpilahti E (1991) Modeling — canopy, photosynthesis, And growth. Physiol Trees 419–444

    Google Scholar 

  • Henry HAL, Aarssen LW (1997) On the relationship between shade tolerance and shade avoidance strategies in woodland plants. Oikos 80:575–582

    Google Scholar 

  • Herbert T (1996) On the relationship of plant geometry to photosynthetic response. In: Mulkey SS, Chazdon RL, Smith AP (eds) Tropical forest plant ecophysiology. Chapman and Hall, New York, pp 139–161

    Google Scholar 

  • Herrera CM (1992) Historical effects and sorting processes as explanations for contemporary ecological patterns: character syndromes in Mediterranean woody plants. Am Nat 140:421–446

    Google Scholar 

  • Herrera CM (1997) Thermal biology and foraging responses of insect pollinators to the forest floor irradiance mosaic. Oikos 78:601–611

    Google Scholar 

  • Hirose T (1987) A vegetative plant growth model: adaptive significance of phenotypic plasticity in dry matter partitioning. Funct Ecol 1:195–202

    Google Scholar 

  • Hoffmann A A, Parsons PA (1991) Evolutionary genetics and environmental stress. Oxford Science Publications, Oxford

    Google Scholar 

  • Holmgren M (2000) Combined effects of shade and drought on tulip poplar seedlings: trade-off in tolerance or facilitation? Oikos 90:67–78

    Google Scholar 

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

    Google Scholar 

  • Jean RV (1984) Mathematical approach to pattern and form in plant growth. Wiley, New York

    Google Scholar 

  • Jean RV, Barabé D (1998) Symmetry in plants. World Scientific Publishing Co Pte Ltd, Singapore

    Google Scholar 

  • Kevan PG (1975) Sun-tracking solar furnaces in high Arctic flowers, Eignificance for pollination and insects. Science 189:723–726

    PubMed  CAS  Google Scholar 

  • Kikuzawa K (1989) Ecology and evolution of phenological pattern, Leaf longevity and leaf habit. Evol Trends Plants 3:105–110

    Google Scholar 

  • Kikuzawa K (1991) A cost benefit analysis of leaf habit and leaf longevity of trees and their geographical pattern. Am Nat 138:1250–1263

    Google Scholar 

  • Kikuzawa K (1995) Leaf phenology as an optimal strategy for carbon gain in plants. Can J Bot 73:158–163

    Google Scholar 

  • Kikuzawa K, Koyama H, Umeki K, Lechowicz MJ (1996) Some evidence for an adaptive linkage between leaf phenology and shoot architecture in sapling trees. Funct Ecol 10:252–257

    Google Scholar 

  • Kiltie RA (1993) New light on forest shade. Trends Ecol Evol 8:39–40

    PubMed  CAS  Google Scholar 

  • King DA (1990) Allometry of saplings and understory trees of a Panamanian forest. Funct Ecol 4:27–32

    Google Scholar 

  • King DA (1991) Correlations between biomass allocation, Relative growth rate and light environment in tropical forest saplings. Funct Ecol 5:485–492

    Google Scholar 

  • Kirchoff BK, Rutishauser R (1990) The phyllotaxy of Costus (Costaceae). Bot Gaz 151:88–105

    Google Scholar 

  • Kohm KA, Franklin JF (1997) Creating a forestry for the 21st century. Island Press, Washington, DC

    Google Scholar 

  • Kohn DD, Walsh DM (1994) Plant species richness — the effect of island size and habitat diversity. J Ecol 82:367–377

    Google Scholar 

  • Kohyama T (1987) Significance of architecture and allometry in saplings. Funct Ecol 1:399–404

    Google Scholar 

  • Kohyama T (1994) Size-structure-based models of forest dynamics to interpret population-and community-level mechanisms. J Plant Res 107:107–116

    Google Scholar 

  • Kohyama T, Hotta M (1990) Significance of allometry in tropical saplings. Funct Ecol 4:515–521

    Google Scholar 

  • Koller D (1990) Light-driven leaf movements. Plant Cell Environ 13:615–632

    Google Scholar 

  • Koller D (2000) Plants in search of sunlight. Adv Bot Res 33:35–131

    CAS  Google Scholar 

  • Kramer K (1994) Selecting a model to predict the onset of growth of Fagus sylvatica. J Appl Ecol 31:172–181

    Google Scholar 

  • Kwesiga FR, Grace J (1986) The role of red/far red ratio in the response of tropical tree seedlings to shade. Ann Bot 57:283–290

    Google Scholar 

  • Kyparissis A, Petropoulou Y, Manetas Y (1995) Summer survival of leaves in a soft-leaved shrub (Phlomis furticosa L. Labiatae) under Mediterranean field conditions: avoidance of photoinhibitory damage through decreased chlorophyll contents. J Exp Bot 46:1825–1831

    CAS  Google Scholar 

  • Larcher W (1995) Physiological plant ecology. Ecophysiology and stress physiology of functional groups. Springer, Berlin Heidelberg New York

    Google Scholar 

  • Latham RE, Ricklefs RE (1993) Global patterns of tree species richness in moist forests: energy-diversity theory does not account for variation in species richness. Oikos 67:325–333

    Google Scholar 

  • Leigh EG (1998) Tropical forest ecology: a view from Barro Colorado Island. Oxford University Press, New York

    Google Scholar 

  • Levin SA, Pacala SW (1997) Theories of simplification and scaling of spatially distributed processes. In: Tilman D, Kareiva P (eds) Spatial ecology: the role of space in population dynamics and interspecific interactions. Princeton University Press, Princeton, NJ, pp 271–295

    Google Scholar 

  • Lin CT (2000) Plant blue-light receptors. Trends Plant Sci 5:337–342

    PubMed  CAS  Google Scholar 

  • Lortie CJ, Aarssen LW (1996) The specialization hypothesis for phenotypic plasticity in plants. Int J Plant Sci 157:484–487

    Google Scholar 

  • Lovelock CE, Clough BF (1992) Influence of solar radiation and leaf angle on leaf xanthophyll concentrations in mangroves. Oecologia 91:518–525

    Google Scholar 

  • Mackerness SAH (2000) Plant responses to ultraviolet-B (UV-B: 280–320 nm) stress: what are the key regulators? Plant Growth Regul 32:27–39

    CAS  Google Scholar 

  • Marshall HL, Geider RJ, Flynn KJ (2000) A mechanistic model of photoinhibition. New Phytol 145:347–359

    Google Scholar 

  • Matsuda K, Bride JR, Kimura M (1989) Seedling growth form of oaks. Ann Bot 64:439–446

    Google Scholar 

  • Mazzella MA, Casai JJ (2001) Interactive signalling by phytochromes and cryptochromes generates de-etiolation homeostasis in Arabidopsis thaliana. Plant Cell Environ 24:155–161

    CAS  Google Scholar 

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

    Google Scholar 

  • Monaco TA, Briske DD (2000) Does resource availability modulate shade avoidance responses to the ratio of red to far-red irradiation? An assessment of radiation quantity and soil volume. New Phytol 146:37–46

    Google Scholar 

  • Nakashizuka T (2001) Species coexistence in temperate, mixed deciduous forests. Trends Ecol Evol 16:205–210

    PubMed  Google Scholar 

  • Nicotra AB, Chazdon RL, Schlichting CD (1997) Patterns of genotypic variation and phenotypic plasticity of light response in two tropical Piper (Piperaceae) species. Am J Bot 84:1542–1552

    PubMed  CAS  Google Scholar 

  • Nicotra AB, Chazdon RL, Iriarte SVB (1999) Spatial heterogeneity of light and woody seedling regeneration in tropical wet forests. Ecology 80:1908–1926

    Google Scholar 

  • Niklas KJ (1988) The role of phyllotactic pattern as a “developmental constraint” on the interception of light by leaf surfaces. Evolution 42:1–16

    Google Scholar 

  • Niklas KJ (1997) The evolutionary biology of plants. University of Chicago Press, Chicago

    Google Scholar 

  • Nilsen ET (1992a) The influence of water stress on leaf and stem photosynthesis in Spartium junceum L. Plant Cell Environ 15:455–461

    Google Scholar 

  • Nilsen ET (1992b) Partitioning growth and photosynthesis between leaves and stems during nitrogen limitation in Spartium junceum. Am J Bot 79:1217–1223

    CAS  Google Scholar 

  • Nilsen ET, Karpa D, Mooney HA, Field C (1993) Patterns of stem photosynthesis in two invasive legumes (Spartium junceum, Cytisus scoparius) of the California coastal region. Am J Bot 80:1126–1136

    Google Scholar 

  • Nishio JN (2000) Why are higher plants green? Evolution of the higher plant photosynthetic pigment complement. Plant Cell Environ 23:539–548

    CAS  Google Scholar 

  • Norman JM, Arkebauer TJ (1991) Predicting canopy light-use efficiency from leaf characteristics. Modeling Plant Soil Systems 31:125–143

    Google Scholar 

  • O’Brien EM, Whittaker RJ, Field R (1998) Climate and woody plant diversity in southern Africa: relationships at species, Genus and family levels. Ecography 21:495–509

    Google Scholar 

  • Osunkoya 00, Ash JE, Hopkins MS, Graham AW (1992) Factors affecting survival of tree seedlings in North Queensland rainforests. Oecologia 91:569–578

    Google Scholar 

  • Pacala SW, Levin SA (1997) Biologically generated spatial pattern and the coexistence of competing species. In: Tilman D, Kareiva P (eds) Spatial ecology: the role of space in population dynamics and interspecific interactions. Princeton University Press, Princeton, NJ, pp 204–232

    Google Scholar 

  • Pacala SW, Rees M (1998) Models suggesting field experiments to test two hypotheses explaining successional diversity. Am Nat 152:729–737

    PubMed  CAS  Google Scholar 

  • Pattison RR, Goldstein G, Ares A (1998) Growth, biomass allocation and photosynthesis of invasive and native Hawaiian rainforest species. Oecologia 117:449–459

    Google Scholar 

  • Pacala SW, Canham CD, Saponara J, Silander JA, Kobe RK, Ribbens E (1996) Forest models defined by field measurements: estimation, Error analysis and dynamics. Ecol Monogr 66:1–43

    Google Scholar 

  • Paul N (2001) Plant responses to UV-B: time to look beyond stratospheric ozone depletion? New Phytol 150:5–8

    Google Scholar 

  • Pearcy RW (1983) The light environment and growth of C3 and C4 tree species in the understory of a Hawaiian forest. Oecologia 58:19–25

    Google Scholar 

  • Pearcy RW (1999) Responses of plants to heterogeneous light environments. In: Pugnaire FI, Valladares F (eds) Handbook of functional plant ecology. Marcel Dekker, New York, pp 269–314

    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 below ground. Academic Press, San Diego, pp 145–174

    Google Scholar 

  • Pearcy RW, Valladares F (1999) Resource acquisition by plants: the role of crown architecture. In: Press M, Scholes JD, Barker MG (eds) Physiological plant ecology. Blackwell Scientific, London, pp 45–66

    Google Scholar 

  • Pearcy RW, Yang W (1996) A three-dimensional shoot architecture model for assessment of light capture and carbon gain by understory plants. Oecologia 108:1–12

    Google Scholar 

  • Pearcy RW, Yang W (1998) The functional morphology of light capture and carbon gain in the redwood-forest understory plant, Adenocaulon bicolor Hook. Funct Ecol 12:543–552

    Google Scholar 

  • Pearcy RW, Sassenrath-Cole GF, Krall JP (1995) Photosynthesis in fluctuating light environments. In: Baker NR (ed) Environmental stress and photosynthesis. Kluwer Academic, The Hague, pp 85–93

    Google Scholar 

  • Perry DA (1998) The scientific basis of forestry. Annu Rev Ecol Syst 29:435–466

    Google Scholar 

  • Pfanz H, Aschan G (2001) The existence of bark and stem photosynthesis in woody plants and its significance for the overall carbon gain. An eco-physiological and ecological approach. Progress in Botany 62. Springer, Berlin Heidelberg New York, pp 477–510

    Google Scholar 

  • Phillips OL, Hall P, Gentry AH, Sawyer SA, Vasquez R (1994) Dynamics and species richness of tropical rain forests. Proc Natl Acad Sci USA 91:2805–2809

    PubMed  CAS  Google Scholar 

  • Pigliucci M (2001) Phenotypic plasticity: beyond nature and nurture. John Hopkins University Press, Baltimore

    Google Scholar 

  • Pollard H, Cruzan M, Pigliucci M (2001) Comparative studies of reaction norms in Arabidopsis. I. Evolution of response to daylength. Evol Ecol Res 3:129–155

    Google Scholar 

  • Pontailler JY, Genty B (1996) A simple red-far-red sensor using gallium arsenide phosphide detectors. Funct Ecol 10:535–540

    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  CAS  Google Scholar 

  • Porembski S, Barthlott W (2000) Biodiversity research in botany. Progress in Botany 61. Springer, Berlin Heidelberg New York, pp 335–362

    Google Scholar 

  • Powles SB, Björkman O (1981) Leaf movement in the shade species Oxalis oregana. II. Role in protection against injury by intense light. Carnegie Inst Wash 80:63–66

    Google Scholar 

  • Press MC (1999) The functional significance of leaf structure: a search for generalizations. New Phytol 143:213–219

    Google Scholar 

  • Prusinkiewicz P (1998) Modeling of spatial structure and development of plants: a review. Sci Hortic 74:113–149

    Google Scholar 

  • Prusinkiewicz P (1999) A look at the visual modeling of plants using L-systems. Agronomie 19:211–224

    Google Scholar 

  • Prusinkiewicz P, Lindenmayer A (1996) The algorithmic beauty of plants. Springer, Berlin Heidelberg New York

    Google Scholar 

  • Pugnaire FI, Luque MT (2001) Changes in plant interactions along a gradient of environmental stress. Oikos 93:42–49

    Google Scholar 

  • Pugnaire FI, Haase P, Puigdefábregas J, Cueto M, Clark SC, Incoll LD (1996) Facilitation and succession under the canopy of a leguminous shrub, Retama sphaerocarpa, In a semi-arid environment in south-east Spain. Oikos 76:455–464

    Google Scholar 

  • Retana J, Espelta JM, Gracia M, Riba M (1999) Seedling recruitment. In: Roda F, Retana J, Gracia C, Bellot J (eds) Ecology of Mediterranean evergreen oak forests. Springer, Berlin Heidelberg New York, pp 89–103

    Google Scholar 

  • Riddoch I, Lehto T, Grace J (1991) Photosynthesis of tropical tree seedlings in relation to light and nutrient supply. New Phytol 119:137–147

    Google Scholar 

  • Room P, Hanan J, Prusinkiewicz P (1996) Virtual plants: new perspectives for ecologists, pathologists and agricultural scientists. Trends Plant Sci 1:33–38

    Google Scholar 

  • Ross J, Sulev M (2000) Sources of errors in measurements of PAR. Agric For Meteorol 100:103

    Google Scholar 

  • Rousseaux MC, Scopel AL, Searles PS, Caldwell MM, Sala OE, Ballare CL (2001) Responses to solar ultraviolet-B radiation in a shrub-dominated natural ecosystem of Tierra del Fuego (southern Argentina). Global Change Biol 7:467–478

    Google Scholar 

  • Sack L, Grubb PJ, Marañon T (2002) The functional morphology of seedlings tolerant of deep shade plus drought in three Mediterranean-climate forests of southern Spain. Plant Ecol (in press)

    Google Scholar 

  • Saxe H, Cannell MGR, Johnsen O, Ryan MG, Vourlitis G (2001) Tree and forest functioning in response to global warming. New Phytol 149:369–400

    CAS  Google Scholar 

  • Scheiner SM (1993) Genetics and evolution of phenotypic plasticity. Annu Rev Ecol Syst 24:35–68

    Google Scholar 

  • Scheiner SM, Callahan HS (1999) Measuring natural selection on phenotypic plasticity. Evolution 53:1704–1713

    Google Scholar 

  • Schlichting CD (1986) The evolution of phenotypic plasticity in plants. Annu Rev Ecol Syst 17:667–693

    Google Scholar 

  • Schlichting CD (1989) Phenotypic integration and environmental change. What are the consequences of differential phenotypic plasticity of traits? Bioscience 39:460–464

    Google Scholar 

  • Schnitzer SA, Carson WP (2001) Treefall gaps and the maintenance of species diversity in a tropical forest. Ecology 82:913–919

    Google Scholar 

  • Sekimura T (1995) The diversity in shoot morphology of herbaceous plants in relation to solar radiation captured by leaves. J Theor Biol 177:289–297

    Google Scholar 

  • Sharitz RR, Boring LR, Van Lear DH, Pinder JE (1992) Integrating ecological concepts with natural resource management of southern forests. Ecol Appl 2:226–237

    Google Scholar 

  • Shipley B, Lechowicz M (2000) The functional co-ordination of leaf morphology, nitrogen concentration, And gas exchange in 40 wetland species. Ecoscience 7:183–194

    Google Scholar 

  • Shirley HL (1929) The influence of light intensity and light quality upon the growth of plants. Am J Bot 16:354

    CAS  Google Scholar 

  • Singsaas EL, Ort DR, DeLucia EV (2001) Variation in measured values of photosynthetic quantum yield in ecophysiological studies. Oecologia 128:15–23

    Google Scholar 

  • Skaltsa H, Verykokidou E, Harvala C, Karabourniotis G, Manetas Y (1994) UV-B protective potential and flavonoid content of leaf hairs of Quercus ilex. Phytochemistry 37:987–990

    CAS  Google Scholar 

  • Smith H (1982) Light quality, photoperception and plant strategy. Annu Rev Plant Physiol 33:481–518

    CAS  Google Scholar 

  • Smith M, Ullberg D (1989) Effect of leaf angle and orientation on photosynthesis and water relations in Silphium terebinthinaceum. Am J Bot 76:1714–1719

    Google Scholar 

  • Smith SD, Osmond CB (1987) Stem photosynthesis in a desert ephemeral, Eriogonum inflatum. Morphology, Stomatal conductance and water use efficiency in field conditions. Oecologia 72:533–541

    Google Scholar 

  • Smith WK, Vogelmann TC, DeLucia EH, Bell DT, Shepherd KA (1997) Leaf form and photosynthesis. Bioscience 47:785–793

    Google Scholar 

  • Soares AG, Scapini F, Brown AC, McLachlan A (1999) Phenotypic plasticity, Genetic similarity and evolutionary inertia in changing environments. J Mollus Stud 65:136–139

    Google Scholar 

  • Stanton ML, Galen C (1993) Blue light controls solar tracking by flowers of an alpine plant. Plant Cell Environ 16:983–989

    Google Scholar 

  • Strauss-Debenedetti S, Bazzaz FA (1991) Plasticity and acclimation to light in tropical moraceae of different successional positions. Oecologia 87:377–387

    Google Scholar 

  • Sultan SE (1987) Evolutionary implications of phenotypic plasticity in plants. Evol Biol 21:127–176

    Google Scholar 

  • Sultan SE (1992) What has survived of Darwin’s theory? Phenotypic plasticity and the Neo-Darwinian legacy. Evol Trends Plants 6:61–71

    Google Scholar 

  • Sultan SE (1995) Phenotypic plasticity and plant adaptation. Acta Bot Neer 44:363–383

    Google Scholar 

  • Sultan SE (2000) Phenotypic plasticity for plant development, Function and life history. Trends Plant Sci 5:537–542

    PubMed  CAS  Google Scholar 

  • Sultan SE, Bazzaz FA (1993) Phenotypic plasticity in Polygonum persicaria. 1. Diversity and uniformity in genotypic norms of reaction to light. Evolution 47:1009–1031

    Google Scholar 

  • Sultan SE, Wilczek AM, Bell DL, Hand G (1998) Physiological response to complex environments in annual Polygonum species of contrasting ecological breadth. Oecologia 115:564–578

    Google Scholar 

  • Tarasjev A (1995) Relationship between phenotypic plasticity and developmental instability in Iris pumila L. Russ J Genet 31:1409–1416

    CAS  Google Scholar 

  • Thornley JHM (1998) Dynamic model of leaf photosynthesis with acclimation to light and nitrogen. Ann Bot 81:421–430

    Google Scholar 

  • Tielborger K, Kadmon R (2000a) Indirect effects in a desert plant community: is competition among annuals more intense under shrub canopies? Plant Ecol 150:53–63

    Google Scholar 

  • Tielborger K, Kadmon R (2000b) Temporal environmental variation tips the balance between facilitation and interference in desert plants. Ecology 81:1544–1553

    Google Scholar 

  • Tilman D (1988) Plant strategies and the dynamics and structure of plant communities. Princeton University Press, Princeton, NJ

    Google Scholar 

  • Tokeshi M (1999) Species coexistence. Ecological and evolutionary perspectives. Blackwell Science, Cambridge

    Google Scholar 

  • Turner IM, Lucas PW, Becker P, Wong SC, Yong JWH, Choong MF, Tyree MT (2000) Tree leaf form in Brunei: a heath forest and a mixed dipterocarp forest compared. Biotropica 32:53–61

    Google Scholar 

  • Valladares F (1999) Architecture, Ecology and evolution of plant crowns. In: Pugnaire FI, Valladares F (eds) Handbook of functional plant ecology. Marcel Dekker, New York, pp 121–194

    Google Scholar 

  • Valladares F (2000) Light and plant evolution: adaptation to the extremes versus phenotypic plasticity. In: Greppin H (ed) Advanced studies in plant biology. University of Geneva, Geneve, pp 341–355

    Google Scholar 

  • Valladares F, Pearcy RW (1997) Interactions between water stress, Sun-shade acclimation, heat tolerance and photoinhibition in the sclerophyll Heteromeles arbutifolia. Plant Cell Environ 20:25–36

    Google Scholar 

  • Valladares F, Pearcy RW (1998) The functional ecology of shoot architecture in sun and shade plants of Heteromeles arbutifolia M. Roem., A Californian chaparral shrub. Oecologia 114:1–10

    Google Scholar 

  • Valladares F, Pearcy RW (1999) The geometry of light interception by shoots of Heteromeles arbutifolia: morphological and physiological consequences for individual leaves. Oecologia 121:171–182

    Google Scholar 

  • Valladares F, Pearcy RW (2000) The role of crown architecture for light harvesting and carbon gain under extreme light conditions assessed with a realistic 3-D model. An Jardin Bot Madr 58:3–16

    Google Scholar 

  • Valladares F, Pearcy RW (2002) Drought can be more critical in the shade than in the sun: a field study of carbon gain and photoinhibition in a Californian shrub during a dry El Niño year. Plant Cell Environ 25:749–759

    Google Scholar 

  • Valladares F, Pugnaire FI (1999) Tradeoffs between irradiance capture and avoidance in semiarid environments simulated with a crown architecture model. Ann Bot 83:459–470

    Google Scholar 

  • Valladares F, Allen MT, Pearcy RW (1997) Photosynthetic response to dynamic light under field conditions in six tropical rainforest shrubs occurring along a light gradient. Oecologia 111:505–514

    Google Scholar 

  • Valladares F, Martinez-Ferri E, Balaguer L, Perez-Corona E, Manrique E (2000a) Low leaf-level response to light and nutrients in Mediterranean evergreen oaks: a conservative resource-use strategy? New Phytol 148:79–91

    CAS  Google Scholar 

  • Valladares F, Wright SJ, Lasso E, Kitajima K, Pearcy RW (2000b) Plastic phenotypic response to light of 16 congeneric shrubs from a Panamanian rainforest. Ecology 81:1925–1936

    Google Scholar 

  • Valladares F, Chico JM, Aranda I, Balaguer L, Dizengremel P, Manrique E, Dreyer E (2002) Greater high light tolerance of seedlings of Quercus robur over Fagus sylvatica is linked to a greater physiological plasticity. Trees Struct Funct (in press)

    Google Scholar 

  • Valladares F, Skillman J, Pearcy RW (2002b) Convergence in light capture efficiencies among tropical forest understory plants with contrasting crown architectures: a case of morphological compensation. Am J Bot 89:1275–1284

    PubMed  Google Scholar 

  • van Klausen M, Fischer M, Schmid B (2000) Costs of plasticity in foraging characteristics of the clonal plant Ranunculus reptans. Evolution 54:1947–1955

    Google Scholar 

  • van Tienderen PH (1991) Evolution of generalists and specialists in spatially heterogeneous environments. Evolution 45:1317–1331

    Google Scholar 

  • Vila M, Sardans J (1999) Plant competition in Mediterranean-type vegetation. J Veg Sei 10:281–294

    Google Scholar 

  • Waller DM (1991) The dynamics of growth and form. In: Crawley MJ (eds) Plant ecology. Blackwell Scientific, Wiltshire, pp 291–320

    Google Scholar 

  • Walters MB, Reich PB (1999) 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 

  • Weiden CW, Hewett SW, Hubbell JG, Foster RB (1991) Sapling survival, Growth, And recruitment: relationship to canopy height in a neotropical forest. Ecology 72:35–50

    Google Scholar 

  • Werner C, Correia O, Beyschlag W (1999) Two different strategies of Mediterranean macchia plants to avoid photoinhibitory damage by excessive radiation levels during summer drought. Acta Oecol 20:15–23

    Google Scholar 

  • Werner C, Ryel RJ, Correia O, Beyschlag W (2001) Effects of photoinhibition on whole-plant carbon gain assessed with a photosynthesis model. Plant Cell Environ 24:27–40

    CAS  Google Scholar 

  • West-Eberhard MJ (1989) Phenotypic plasticity and the origins of diversity. Annu Rev Ecol Syst 20:249–278

    Google Scholar 

  • Wilder GJ (1992) Orthodistichous phyllotaxy and dorsiventral symmetry on adult shoots of Cyclanthus bipartitus (Cyclanthaceae, Monocotyledoneae). Can J Bot 70:1388–1400

    Google Scholar 

  • Wilson JB, Agnew ODQ (1992) Positive feedback switches in plant communities. Adv Ecol Res 20:265–336

    Google Scholar 

  • Wirtz KW (2000) Simulating the dynamics of leaf physiology and morphology with an extended optimality approach. Ann Bot 86:753–764

    Google Scholar 

  • Wright SJ (2002) Plant diversity in tropical forests: a review of mechanisms of species coexistence. Oecologia 130:1–14

    Google Scholar 

  • Young AJ (1991) The photoprotective role of carotenoids in higher plants. Physiol Plant 83:702–708

    CAS  Google Scholar 

  • Zavala MA, Oria JA (1995) Preserving biological diversity in managed forests: a meeting point for ecology and forestry. Landscape Urban Planning 31:363–378

    Google Scholar 

  • Zavala MA, Espeita JM, Retana J (2000) Constraints and trade-offs in Mediterranean plant communities: the case of Holm oak-Aleppo pine forests. Bot Rev 66:119–149

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Editor information

Editors and Affiliations

Rights and permissions

Reprints and permissions

Copyright information

© 2003 Springer-Verlag Berlin Heidelberg

About this chapter

Cite this chapter

Valladares, F. (2003). Light Heterogeneity and Plants: from Ecophysiology to Species Coexistence and Biodiversity. In: Esser, K., Lüttge, U., Beyschlag, W., Hellwig, F. (eds) Progress in Botany. Progress in Botany, vol 64. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-55819-1_17

Download citation

  • DOI: https://doi.org/10.1007/978-3-642-55819-1_17

  • Publisher Name: Springer, Berlin, Heidelberg

  • Print ISBN: 978-3-642-62838-2

  • Online ISBN: 978-3-642-55819-1

  • eBook Packages: Springer Book Archive

Publish with us

Policies and ethics