Investigating the European beech (Fagus sylvatica L.) leaf characteristics along the vertical canopy profile: leaf structure, photosynthetic capacity, light energy dissipation and photoprotection mechanisms.

Forest functionality and productivity are directly related to canopy light interception and can be affected by potential damage from high irradiance. However, the mechanisms by which leaves adapt to the variable light environments along the multilayer canopy profile are still poorly known. We explored the leaf morphophysiological and metabolic responses to the natural light gradient in a pure European beech (Fagus sylvatica L.) forest at three different canopy heights (top, middle and bottom). Structural adjustment through light-dependent modifications in leaf mass per area was the reason for most of the variations in photosynthetic capacity. The different leaf morphology along the canopy influenced nitrogen (N) partitioning, water- and photosynthetic N-use efficiency, chlorophyll (Chl) fluorescence and quali-quantitative contents of photosynthetic pigments. The Chl a to Chl b ratio and the pool of xanthophyll-cycle pigments (VAZ) increased at the highest irradiance, as well as lutein and β-carotene. The total pool of ascorbate and phenols was higher in leaves of the top and middle canopy layers when compared with the bottom layer, where the ascorbate peroxidase was relatively more activated. The non-photochemical quenching was strongly and positively related to the VAZ/(Chl a + b) ratio, while Chl a/Chl b was related to the photochemical efficiency of photosystem II. Along the multilayer canopy profile, the high energy dissipation capacity of leaves was correlated to an elevated redox potential of antioxidants. The middle layer gave the most relevant contribution to leaf area index and carboxylation capacity of the canopy. In conclusion, a complex interplay among structural, physiological and biochemical traits drives the dynamic leaf acclimation to the natural gradients of variable light environments along the tree canopy profile. The relevant differences observed in leaf traits within the canopy positions of the beech forest should be considered for improving estimation of carbon fluxes in multilayer canopy models of temperate forests.

[1]  Y. Manetas,et al.  Enhanced UV-B radiation under field conditions increases anthocyanin and reduces the risk of photoinhibition but does not affect growth in the carnivorous plant Pinguicula vulgaris , 1999 .

[2]  W. Chow,et al.  Dynamic flexibility in the structure and function of photosystem II in higher plant thylakoid membranes: the grana enigma , 2008, Photosynthesis Research.

[3]  Ü. Niinemets,et al.  Do the capacity and kinetics for modification of xanthophyll cycle pool size depend on growth irradiance in temperate trees , 2003 .

[4]  Luca Sebastiani,et al.  Could the differences in O3 sensitivity between two poplar clones be related to a difference in antioxidant defense and secondary metabolic response to O3 influx , 2008 .

[5]  R. Bassi,et al.  Carotenoids: Localization and Function , 1996 .

[6]  W. W. Adams,et al.  Photoprotection in an ecological context: the remarkable complexity of thermal energy dissipation. , 2006, The New phytologist.

[7]  Michael L. Roderick,et al.  Pinatubo, Diffuse Light, and the Carbon Cycle , 2003, Science.

[8]  Ü. Rannik,et al.  Estimates of the annual net carbon and water exchange of forests: the EUROFLUX methodology , 2000 .

[9]  D. Di Baccio,et al.  Seawater irrigation: antioxidant defence responses in leaves and roots of a sunflower (Helianthus annuus L.) ecotype. , 2004, Journal of plant physiology.

[10]  J. Berry,et al.  A biochemical model of photosynthetic CO2 assimilation in leaves of C3 species , 1980, Planta.

[11]  A. Ruban Evolution under the sun: optimizing light harvesting in photosynthesis. , 2015, Journal of experimental botany.

[12]  G. Matteucci,et al.  Comparisons of δ13C of photosynthetic products and ecosystem respiratory CO2 and their responses to seasonal climate variability , 2004, Oecologia.

[13]  H. Lichtenthaler,et al.  Chlorophyll fluorescence kinetics, photosynthetic activity, and pigment composition of blue-shade and half-shade leaves as compared to sun and shade leaves of different trees , 2013, Photosynthesis Research.

[14]  J. García-Plazaola,et al.  Seasonal changes in photosynthetic pigments and antioxidants in beech (Fagus sylvatica) in a Mediterranean climate: implications for tree decline diagnosis , 2001 .

[15]  Martin Navrátil,et al.  Impact of clear and cloudy sky conditions on the vertical distribution of photosynthetic CO2 uptake within a spruce canopy , 2012 .

[16]  Ü. Niinemets,et al.  Shade Tolerance, a Key Plant Feature of Complex Nature and Consequences , 2008 .

[17]  J. Lewis,et al.  Vertical gradients in photosynthetic light response within an old-growth Douglas-fir and western hemlock canopy. , 2000, Tree physiology.

[18]  H. Lichtenthaler,et al.  Induction of photosynthesis and importance of limitations during the induction phase in sun and shade leaves of five ecologically contrasting tree species from the temperate zone. , 2007, Tree physiology.

[19]  S. Fleck,et al.  Within-canopy variation in photosynthetic capacity, SLA and foliar N in temperate broad-leaved trees with contrasting shade tolerance , 2014, Trees.

[20]  M. M. Bradford A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding. , 1976, Analytical biochemistry.

[21]  S. Fry,et al.  Antioxidants and Reactive Oxygen Species in Plants , 2005 .

[22]  A. Iio,et al.  Vertical, horizontal and azimuthal variations in leaf photosynthetic characteristics within a Fagus crenata crown in relation to light acclimation. , 2005, Tree physiology.

[23]  Ü. Niinemets,et al.  Acclimation of antioxidant pools to the light environment in a natural forest canopy. , 2004, The New phytologist.

[24]  J. Briantais,et al.  The relationship between the quantum yield of photosynthetic electron transport and quenching of chlorophyll fluorescence , 1989 .

[25]  U. Hansen,et al.  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 , 2002, Trees.

[26]  John Tenhunen,et al.  A model separating leaf structural and physiological effects on carbon gain along light gradients for the shade‐tolerant species Acer saccharum , 1997 .

[27]  G. Matteucci,et al.  Seasonal and inter-annual dynamics of growth, non-structural carbohydrates and C stable isotopes in a Mediterranean beech forest. , 2013, Tree physiology.

[28]  E. Paoletti,et al.  Could the differences in O(3) sensitivity between two poplar clones be related to a difference in antioxidant defense and secondary metabolic response to O(3) influx? , 2008, Tree physiology.

[29]  Alexander Ac,et al.  Differences in pigment composition, photosynthetic rates and chlorophyll fluorescence images of sun and shade leaves of four tree species. , 2007, Plant physiology and biochemistry : PPB.

[30]  Jurij Diaci,et al.  Gap size and position influence variable response of Fagus sylvatica L. and Abies alba Mill. , 2014 .

[31]  R. Tognetti,et al.  Early responses to cadmium of two poplar clones that differ in stress tolerance. , 2014, Journal of plant physiology.

[32]  Peter E. Thornton,et al.  An Improved Canopy Integration Scheme for a Land Surface Model with Prognostic Canopy Structure , 2007 .

[33]  Carl J. Bernacchi,et al.  Improved temperature response functions for models of Rubisco‐limited photosynthesis , 2001 .

[34]  S. Veres,et al.  Responses of leaf traits of European beech (Fagus sylvatica L.) saplings to supplemental UV-B radiation and UV-B exclusion , 2009 .

[35]  G. Matteucci,et al.  Effect of environmental variables and stand structure on ecosystem respiration components in a Mediterranean beech forest. , 2013, Tree physiology.

[36]  J. Tenhunen,et al.  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 , 1998 .

[37]  V. L. Singleton,et al.  Colorimetry of Total Phenolics with Phosphomolybdic-Phosphotungstic Acid Reagents , 1965, American Journal of Enology and Viticulture.

[38]  Antonio Donato Nobre,et al.  Acclimation of photosynthetic capacity to irradiance in tree canopies in relation to leaf nitrogen concentration and leaf mass per unit area , 2002 .

[39]  M. Liddell,et al.  Canopy position affects the relationships between leaf respiration and associated traits in a tropical rainforest in Far North Queensland. , 2014, Tree physiology.

[40]  B. Pogson,et al.  Lutein from Deepoxidation of Lutein Epoxide Replaces Zeaxanthin to Sustain an Enhanced Capacity for Nonphotochemical Chlorophyll Fluorescence Quenching in Avocado Shade Leaves in the Dark1 , 2011, Plant Physiology.

[41]  G. Noctor Metabolic signalling in defence and stress: the central roles of soluble redox couples. , 2006, Plant, cell & environment.

[42]  I. Terashima,et al.  Why are Sun Leaves Thicker than Shade Leaves? — Consideration based on Analyses of CO2 Diffusion in the Leaf , 2001, Journal of Plant Research.

[43]  H. Lichtenthaler,et al.  Differences in photosynthetic activity, chlorophyll and carotenoid levels, and in chlorophyll fluorescence parameters in green sun and shade leaves of Ginkgo and Fagus. , 2007, Journal of plant physiology.

[44]  S. Grace Phenolics as Antioxidants , 2007 .

[45]  K. Niyogi,et al.  Non-photochemical quenching. A response to excess light energy. , 2001, Plant physiology.

[46]  M. Naramoto,et al.  Photosynthetic capacity and nitrogen partitioning in foliage of the evergreen shrub Daphniphyllum humile along a natural light gradient. , 2007, Tree physiology.

[47]  G. Grassi,et al.  Foliar morphological and physiological plasticity in Picea abies and Abies alba saplings along a natural light gradient. , 2001, Tree physiology.

[48]  G. Matteucci,et al.  Short-term natural δ 13 C and δ 18 O variations in pools and fluxes in a beech forest: the transfer of isotopic signal from recent photosynthates to soil respired CO 2 , 2011 .

[49]  U. Niinemets Improving modeling of the 'dark part' of canopy carbon gain. , 2014, Tree physiology.

[50]  A. Granier,et al.  Seasonal time-course of gradients of photosynthetic capacity and mesophyll conductance to CO2 across a beech (Fagus sylvatica L.) canopy. , 2009, Journal of experimental botany.

[51]  K. Hikosaka,et al.  Photosynthesis or persistence: nitrogen allocation in leaves of evergreen and deciduous Quercus species , 2004 .

[52]  W. Seiler,et al.  Potential risks for European beech (Fagus sylvatica L.) in a changing climate , 2006, Trees.

[53]  F. Loreto,et al.  The use of low [CO2] to estimate diffusional and non‐diffusional limitations of photosynthetic capacity of salt‐stressed olive saplings , 2003 .

[54]  J. Peñuelas,et al.  Morphological, biochemical and physiological traits of upper and lower canopy leaves of European beech tend to converge with increasing altitude. , 2015, Tree physiology.

[55]  A. Scartazza,et al.  Zeaxanthin and non-photochemical quenching in sun and shade leaves of C3 and C4 plants , 1998 .

[56]  A. Cutini,et al.  Estimation of leaf area index with the Li-Cor LAI 2000 in deciduous forests , 1998 .

[57]  Ü. Niinemets,et al.  Photosynthetic acclimation to simultaneous and interacting environmental stresses along natural light gradients: optimality and constraints. , 2004, Plant biology.

[58]  P. Mullineaux,et al.  Photosynthetic electron transport regulates the expression of cytosolic ascorbate peroxidase genes in Arabidopsis during excess light stress. , 1997, The Plant cell.

[59]  M. Faust,et al.  Changes in ascorbate, glutathione, and related enzyme activities during thidiazuron‐induced bud break of apple , 1991 .

[60]  U. Niinemets,et al.  Photosynthesis and resource distribution through plant canopies. , 2007, Plant, cell & environment.

[61]  G. Matteucci,et al.  Combining stable isotope and carbohydrate analyses in phloem sap and fine roots to study seasonal changes of source-sink relationships in a Mediterranean beech forest. , 2015, Tree physiology.

[62]  Lea Hallik,et al.  A worldwide analysis of within-canopy variations in leaf structural, chemical and physiological traits across plant functional types. , 2015, The New phytologist.

[63]  Carl J. Bernacchi,et al.  In vivo temperature response functions of parameters required to model RuBP-limited photosynthesis , 2003 .

[64]  O. Urban,et al.  Ultraviolet and photosynthetically active radiation can both induce photoprotective capacity allowing barley to overcome high radiation stress. , 2015, Plant physiology and biochemistry : PPB.

[65]  C. Foyer,et al.  ASCORBATE AND GLUTATHIONE: Keeping Active Oxygen Under Control. , 1998, Annual review of plant physiology and plant molecular biology.

[66]  K. Oleson,et al.  Reconciling leaf physiological traits and canopy flux data: Use of the TRY and FLUXNET databases in the Community Land Model version 4 , 2012 .