Three-dimensional lamina architecture alters light-harvesting efficiency in Fagus: a leaf-scale analysis.

Modification of foliage exposition and morphology by seasonal average integrated quantum flux density (Qint) was investigated in the canopies of the shade-tolerant late-successional deciduous tree species Fagus orientalis Lipsky and Fagus sylvatica L. Because the leaves were not entirely flat anywhere in the canopy, the leaf lamina was considered to be three-dimensional and characterized by the cross-sectional angle between the leaf halves (theta). Both branch and lamina inclination angles with respect to the horizontal scaled positively with irradiance in the canopy, allowing light to penetrate to deeper canopy horizons. Lamina cross-sectional angle varied from 170 degrees in the most shaded leaves to 90-100 degrees in leaves in the top of the canopy. Thus, the degree of leaf rolling increased with increasing Qint, further reducing the light-interception efficiency of the upper-canopy leaves. Simulations of the dependence of foliage light-interception efficiency on theta demonstrated that decreases in theta primarily reduce the interception efficiency of direct irradiance, but that diffuse irradiance was equally efficiently intercepted over the entire range of theta values in our study. Despite strong alteration in foliage light-harvesting capacity within the canopy and greater transmittance of the upper crown compared with the lower canopy, mean incident irradiances varied more than 20-fold within the canopy, indicating inherent limitations in light partitioning within the canopy. This extensive canopy light gradient was paralleled by plastic changes in foliar structure and chemistry. Leaf dry mass per unit area varied 3-4-fold between the canopy top and bottom, providing an important means of scaling foliage nitrogen contents and photosynthetic capacity per unit area with Qint. Although leaf structure versus light relationships were qualitatively similar in all cases, there were important tree-to-tree and species-to-species variations, as well as evidence of differences in investments in structural compounds within the leaf lamina, possibly in response to contrasting leaf water availability in different trees.

[1]  T. Nilson A theoretical analysis of the frequency of gaps in plant stands , 1971 .

[2]  S. Fleck,et al.  Petiole mechanics, leaf inclination, morphology, and investment in support in relation to light availability in the canopy of Liriodendron tulipifera , 2002, Oecologia.

[3]  M. Jackson Hormones from roots as signals for the shoots of stressed plants , 1997 .

[4]  Gravity-induced effects on material properties and size of leaves on horizontal shoots of Acer saccharum (Aceraceae) , 1992 .

[5]  K. Niklas Petiole mechanics, light interception by Lamina, and “Economy in Design” , 1992, Oecologia.

[6]  Byron B. Lamont,et al.  Leaf specific mass confounds leaf density and thickness , 1991, Oecologia.

[7]  K. Niklas FLEXURAL STIFFNESS ALLOMETRIES OF ANGIOSPERM AND FERN PETIOLES AND RACHISES: EVIDENCE FOR BIOMECHANICAL CONVERGENCE , 1991, Evolution; international journal of organic evolution.

[8]  O. Kull,et al.  Stoichiometry of foliar carbon constituents varies along light gradients in temperate woody canopies: implications for foliage morphological plasticity. , 1998, Tree physiology.

[9]  John L. Innes,et al.  Observations on the Condition of Beech (Fagus sylvatica L.) in Britain in 1990 , 1992 .

[10]  P. Kramer,et al.  Morphological adaptations of leaves to water stress. , 1980 .

[11]  Yoshioka,et al.  Expression of genes responsible for ethylene production and wilting are differently regulated in carnation (Dianthus caryophyllus L.) petals. , 2000, Plant science : an international journal of experimental plant biology.

[12]  D. Fernández,et al.  Maize Leaf Rolling Initiation , 1999, Photosynthetica.

[13]  S. James,et al.  Leaf Orientation in Juvenile Eucalyptus camaldulensis , 1996 .

[14]  P. Reich,et al.  Leaf age and season influence the relationships between leaf nitrogen, leaf mass per area and photosynthesis in maple and oak trees , 1991 .

[15]  D. Hollinger Optimality and nitrogen allocation in a tree canopy. , 1996, Tree physiology.

[16]  Hervé Sinoquet,et al.  Foliage determinants of light interception in sunny and shaded branches of Fagus sylvatica (L.) , 1998 .

[17]  Dennis D. Baldocchi,et al.  Solar radiation within an oak—hickory forest: an evaluation of the extinction coefficients for several radiation components during fully-leafed and leafless periods , 1984 .

[18]  Yanhong Tang,et al.  Flexible Leaf Orientations of Arisaema heterophyllum Maximize Light Capture in a Forest Understorey and Avoid Excess Irradiance at a Deforested Site , 1998 .

[19]  G. W. Davis,et al.  Photosynthetic responses of heliophilous Rhus species to environmental modification by invasive shrubs , 1992 .

[20]  S. Fleck,et al.  Leaf Biomechanics and Biomass Investment in Support in Relation to Long-Term Irradiance in Fagus , 2002 .

[21]  J. M. Norman,et al.  Plant Canopies: Their Growth, Form and Function: The description and measurement of plant canopy structure , 1989 .

[22]  H. Mayer,et al.  Wälder der Türkei , 1986 .

[23]  H. Sinoquet,et al.  Characterization of the Light Environment in Canopies Using 3D Digitising and Image Processing , 1998 .

[24]  Elias Fereres,et al.  Responses of Young Almond Trees to Two Drought Periods in the Field , 1982 .

[25]  M. Sulev,et al.  Sources of errors in measurements of PAR , 2000 .

[26]  D. Ellsworth,et al.  Dependence of needle architecture and chemical composition on canopy light availability in three North American Pinus species with contrasting needle length. , 2002, Tree physiology.

[27]  Robert W. Pearcy,et al.  The functional morphology of light capture and carbon gain in the Redwood forest understorey plant Adenocaulon bicolor Hook , 1998 .

[28]  T. Toma,et al.  Leaf gas exchange and cholorphyll fluorescence in relation to leaf angle, azimuth, and canopy position in the tropical pioneer tree, Macaranga conifera. , 1999, Tree physiology.

[29]  R. Peters Ecology of beech forests in the northern hemisphere. , 1992 .

[30]  B. E. Mahall,et al.  Quantitative Phenology and Water Relations of an Evergreen and a Deciduous Chaparral Shrub , 1986 .

[31]  PHYSIOLOGICAL AND MORPHOLOGICAL MODIFICATIONS OF PLANTAGO MAJOR (PLANTAGINACEAE) IN RESPONSE TO LIGHT CONDITIONS , 1989 .

[32]  F. W. Wiegel,et al.  Optimizing the Canopy Photosynthetic Rate by Patterns of Investment in Specific Leaf Mass , 1988, The American Naturalist.

[33]  Mathias Disney,et al.  Monte Carlo ray tracing in optical canopy reflectance modelling , 2000 .

[34]  T. W. Halstead,et al.  Plants in space. , 1987, Annual review of plant physiology.

[35]  F. Bussotti,et al.  Morpho-anatomical aterations in leaves of Gagus vatica L. and Quercus ilex L. in different environmental stress condition , 1998 .

[36]  M. Abrams,et al.  Relating Wet and Dry Year Ecophysiology to Leaf Structure in Contrasting Temperate Tree Species , 1994 .

[37]  K. Niklas Differences between Acer saccharum Leaves from Open and Wind-Protected Sites , 1996 .

[38]  R. Savé,et al.  Effects of water stress and rewatering on leaf water relations of lemon plants , 1997, Biologia Plantarum.

[39]  Robert W. Pearcy,et al.  A three-dimensional crown architecture model for assessment of light capture and carbon gain by understory plants , 1996, Oecologia.

[40]  A. Cescatti Modelling the radiative transfer in discontinuous canopies of asymmetric crowns. I. Model structure and algorithms , 1997 .

[41]  H Sinoquet,et al.  Canopy structure and light interception in Quercus petraea seedlings in relation to light regime and plant density. , 2001, Tree physiology.

[42]  Akira Osawa,et al.  Measurement of three‐dimensional structure of plants with a simple device and estimation of light capture of individual leaves , 1998 .

[43]  Hervé Cochard,et al.  Drought‐induced leaf shedding in walnut: evidence for vulnerability segmentation , 1993 .

[44]  J. Ross The radiation regime and architecture of plant stands , 1981, Tasks for vegetation sciences 3.

[45]  G. Thillart,et al.  Society for Experimental Biology Seminar Series , 1991 .

[46]  H. Drew Economy in Design , 1944 .

[47]  Robert W. Pearcy,et al.  The functional ecology of shoot architecture in sun and shade plants of Heteromeles arbutifolia M. Roem., a Californian chaparral shrub , 1998, Oecologia.

[48]  F.W.T. Penning de Vries,et al.  A rapid method for determining the efficiency of biosynthesis of plant biomass , 1987 .

[49]  B. Pickard Early events in geotropism of seedling shoots. , 1985, Annual review of plant physiology.

[50]  S. Heckathorn,et al.  Effect of Leaf Rolling on Gas Exchange and Leaf Temperature of Andropogon gerardii and Spartina pectinata , 1991, Botanical Gazette.