Complex adjustments of photosynthetic potentials and internal diffusion conductance to current and previous light availabilities and leaf age in Mediterranean evergreen species Quercus ilex.

Mature non-senescent leaves of evergreen species become gradually shaded as new foliage develops and canopy expands, but the interactive effects of integrated light during leaf formation (Q(int)G), current light (Q(int)C) and leaf age on foliage photosynthetic competence are poorly understood. In Quercus ilex L., we measured the responses of leaf structural and physiological variables to Q(int)C and Q(int)G for four leaf age classes. Leaf aging resulted in increases in leaf dry mass per unit area (M(A)), and leaf dry to fresh mass ratio (D(F)) and decreases in N content per dry mass (N(M)). N content per area (N(A)) was independent of age, indicating that decreases in N(M) reflected dilution of leaf N because of accumulation of dry mass (NA = N(M) M(A)). M(A), D(F) and N(A) scaled positively with irradiance, whereas these age-specific correlations were stronger with leaf growth light than with current leaf light. Area-based maximum ribulose 1,5-bisphosphate carboxylase/oxygenase (Rubisco) carboxylase activity (V(cmax)A), capacity for photosynthetic electron transport (J(max)A) and the rate of non-photorespiratory respiration in light (R(d)A) were also positively associated with irradiance. Differently from leaf structural characteristics, for all data pooled, these relationships were stronger with current light with little differences among leaves of different age. Acclimation to current leaf light environment was achieved by light-dependent partitioning of N in rate-limiting proteins. Mass-based physiological activities decreased with increasing leaf age, reflecting dilution of leaf N and a larger fraction of non-photosynthetic N in older leaves. This resulted in age-dependent modification of leaf photosynthetic potentials versus N relationships. Internal diffusion conductance (g(m)) per unit area (g(m)A) increased curvilinearly with increasing irradiance for two youngest leaf age classes and was independent of light for older leaves. In contrast, g(m) per dry mass (g(m)M) was negatively associated with light in current-year leaves. Greater photosynthetic potentials and moderate changes in diffusion conductance resulted in greater internal diffusion limitations of photosynthesis in higher light. Both area- and mass-based g(m) decreased with increasing leaf age. The decrease in diffusion conductance was larger than changes in photosynthetic potentials, leading to larger CO2 drawdown from leaf internal air space to chloroplasts (delta(c)) in older leaves. The increases in diffusion limitations in older leaves and at higher light scaled with age- and light-dependent increases in MA and D(F). Overall, our study demonstrates a large potential of foliage photosynthetic acclimation to changes in leaf light environment, but also highlights enhanced structural diffusion limitations in older leaves that result from leaf structural acclimation to previous rather than to current light environment and accumulation of structural compounds with leaf age.

[1]  John R. Evans,et al.  Profiles of light absorption and chlorophyll within spinach leaves from chlorophyll fluorescence , 2002 .

[2]  I. Terashima,et al.  Construction and maintenance of the optimal photosynthetic systems of the leaf, herbaceous plant and tree: an eco-developmental treatise. , 2004, Annals of botany.

[3]  D. Whitehead,et al.  The relative limitation of photosynthesis by mesophyll conductance in co-occurring species in a temperate rainforest dominated by the conifer Dacrydium cupressinum. , 2003, Functional plant biology : FPB.

[4]  Ü. Niinemets,et al.  Controls on the emission of plant volatiles through stomata: A sensitivity analysis , 2003 .

[5]  Isric FAO - Unesco Soil map of the world : revised legend with corrections and updates , 1997 .

[6]  Ü. Niinemets,et al.  Acclimation to low irradiance in Picea abies: influences of past and present light climate on foliage structure and function. , 1997, Tree physiology.

[7]  I. Terashima,et al.  The effect of growth irradiance on leaf anatomy and photosynthesis in Acer species differing in light demand , 2002 .

[8]  A. Cescatti,et al.  Leaf internal diffusion conductance limits photosynthesis more strongly in older leaves of Mediterranean evergreen broad‐leaved species , 2005 .

[9]  D. Sims,et al.  Photosynthetic characteristics of a tropical forest understory herb, Alocasia macrorrhiza, and a related crop species, Colocasia esculenta grown in contrasting light environments , 1989, Oecologia.

[10]  J. M. Norman,et al.  Partitioning solar radiation into direct and diffuse, visible and near-infrared components , 1985 .

[11]  A. Held,et al.  Dark Leaf Respiration in Light and Darkness of an Evergreen and a Deciduous Plant Species , 1995, Plant physiology.

[12]  F. Loreto,et al.  Acquisition and Diffusion of CO2 in Higher Plant Leaves , 2000 .

[13]  I. Terashima,et al.  The influence of leaf thickness on the CO2 transfer conductance and leaf stable carbon isotope ratio for some evergreen tree species in Japanese warm‐temperate forests , 1999 .

[14]  F. Magnani,et al.  Stomatal, mesophyll conductance and biochemical limitations to photosynthesis as affected by drought and leaf ontogeny in ash and oak trees , 2005 .

[15]  I. Terashima,et al.  CO2 transfer conductance, leaf structure and carbon isotope composition of Polygonum cuspidatum leaves from low and high altitudes , 2001 .

[16]  Ü. Niinemets,et al.  Structural determinants of leaf light-harvesting capacity and photosynthetic potentials , 2006 .

[17]  Tadaki Hirose,et al.  Does the photosynthetic light-acclimation need change in leaf anatomy? , 2003 .

[18]  T. Sharkey,et al.  Theoretical Considerations when Estimating the Mesophyll Conductance to CO(2) Flux by Analysis of the Response of Photosynthesis to CO(2). , 1992, Plant physiology.

[19]  J. Tenhunen,et al.  Limitations due to water stress on leaf net photosynthesis of Quercus coccifera in the Portuguese evergreen scrub , 1985, Oecologia.

[20]  Susanne von Caemmerer,et al.  Temperature Response of Mesophyll Conductance. Implications for the Determination of Rubisco Enzyme Kinetics and for Limitations to Photosynthesis in Vivo , 2002, Plant Physiology.

[21]  T. W. Ridler,et al.  Picture thresholding using an iterative selection method. , 1978 .

[22]  T. Sharkey,et al.  Diffusive and metabolic limitations to photosynthesis under drought and salinity in C(3) plants. , 2004, Plant biology.

[23]  S. Naidu,et al.  Acclimation of shade-developed leaves on saplings exposed to late-season canopy gaps. , 1997, Tree physiology.

[24]  Ichiro Terashima,et al.  Comparative ecophysiology of leaf and canopy photosynthesis , 1995 .

[25]  Pol Coppin,et al.  Assessment of automatic gap fraction estimation of forests from digital hemispherical photography , 2005 .

[26]  F. Loreto,et al.  Photosynthetic limitations in olive cultivars with different sensitivity to salt stress , 2003 .

[27]  J. Tenhunen,et al.  Interactive effects of nitrogen and phosphorus on the acclimation potential of foliage photosynthetic properties of cork oak, Quercus suber, to elevated atmospheric CO2 concentrations , 1999 .

[28]  John Doe,et al.  Soil Map of the World , 1962 .

[29]  I. Terashima,et al.  Changes in mesophyll anatomy and sink–source relationships during leaf development in Quercus glauca, an evergreen tree showing delayed leaf greening , 2003 .

[30]  G. Russell,et al.  Leaf area index estimates obtained for clumped canopies using hemispherical photography , 1999 .

[31]  S. Rambal,et al.  Optimization of carbon gain in canopies of mediterranean evergreen oaks , 1996 .

[32]  Markus Reichstein,et al.  Drought controls over conductance and assimilation of a Mediterranean evergreen ecosystem: scaling from leaf to canopy , 2003 .

[33]  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 .

[34]  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 .

[35]  E. Garnier,et al.  Leaf anatomy, specific mass and water content in congeneric annual and perennial grass species , 1994 .

[36]  John R. Evans,et al.  Determination of the Average Partial Pressure of CO2 in Chloroplasts From Leaves of Several C3 Plants , 1991 .

[37]  C. Field,et al.  Scaling Physiological Processes: Leaf to Globe , 1995 .

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

[39]  John R. Evans,et al.  Photosynthetic acclimation of plants to growth irradiance: the relative importance of specific leaf area and nitrogen partitioning in maximizing carbon gain , 2001 .

[40]  T. Sharkey,et al.  Measurements of mesophyll conductance, photosynthetic electron transport and alternative electron sinks of field grown wheat leaves , 1994, Photosynthesis Research.

[41]  G. Edwards,et al.  Can CO2 assimilation in maize leaves be predicted accurately from chlorophyll fluorescence analysis? , 1993, Photosynthesis Research.

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

[43]  R. Ceulemans,et al.  Leaf-level phenotypic variability and plasticity of invasive Rhododendron ponticum and non-invasive Ilex aquifolium co-occurring at two contrasting European sites. , 2003, Plant, cell & environment.

[44]  J. Tenhunen,et al.  Canopy structure within a Quercus ilex forested watershed: variations due to location, phenological development, and water availability , 1994, Trees.

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

[46]  P. Nobel,et al.  Internal Leaf Area and Cellular CO2 Resistance: Photosynthetic Implications of Variations with Growth Conditions and Plant Species , 1977 .

[47]  I. Terashima,et al.  Effects of leaf age on internal CO2 transfer conductance and photosynthesis in tree species having different types of shoot phenology , 2001 .

[48]  W. Larcher,et al.  Bioclima e potenziale di produttivitá di Quercus ilex L. al limite settentrionale dell'areale di distribuzione. Parte III. Adattamento morfologico e funzionale delle foglie alle radiazioni luminose , 1991 .

[49]  Ian J. Wright,et al.  World-wide leaf economics spectrum , 2004 .

[50]  E. Ögren,et al.  Photosynthetic light-response curves , 1993, Planta.

[51]  J. Tenhunen,et al.  Spatial and age-dependent modifications of photosynthetic capacity in four Mediterranean oak species. , 2004, Functional plant biology : FPB.

[52]  M. Adams,et al.  Distribution of N, Rubisco and photosynthesis in Pinus pinaster and acclimation to light , 2001 .

[53]  S. Rambal,et al.  Seasonal and annual changes in leaf δ13C in two co-occurring Mediterranean oaks: relations to leaf growth and drought progression , 1998 .

[54]  S. von Caemmerer,et al.  Carbon Dioxide Diffusion inside Leaves , 1996, Plant physiology.

[55]  John R. Evans,et al.  Profiles of 14C fixation through spinach leaves in relation to light absorption and photosynthetic capacity , 2003 .

[56]  D. Sprugel,et al.  The effects of light acclimation during and after foliage expansion on photosynthesis ofAbies amabilis foliage within the canopy , 1996, Oecologia.

[57]  A. Bombelli,et al.  Correlation between leaf age and other leaf traits in three Mediterranean maquis shrub species: Quercus ilex, Phillyrea latifolia and Cistus incanus , 2000 .

[58]  Susan E. Lee,et al.  Predicting the Future Productivity and Distribution of Global Terrestrial Vegetation , 2001 .

[59]  D. Jordan,et al.  The CO2/O2 specificity of ribulose 1,5-bisphosphate carboxylase/oxygenase , 1984, Planta.

[60]  D. Sprugel,et al.  Acclimation responses of mature Abies amabilis sun foliage to shading , 1994, Oecologia.

[61]  Ü. Niinemets,et al.  Needle longevity, shoot growth and branching frequency in relation to site fertility and within-canopy light conditions in Pinus sylvestris , 2003 .

[62]  R. J. Spreitzer Questions about the complexity of chloroplast ribulose-1,5-bisphosphate carboxylase/oxygenase , 1999, Photosynthesis Research.

[63]  I. Terashima,et al.  Effects of HgCl(2) on CO(2) dependence of leaf photosynthesis: evidence indicating involvement of aquaporins in CO(2) diffusion across the plasma membrane. , 2002, Plant & cell physiology.

[64]  T. Sharkey,et al.  Estimation of Mesophyll Conductance to CO(2) Flux by Three Different Methods. , 1992, Plant physiology.

[65]  J. Infante Modelling transpiration in holm-oak savannah: scaling up from the leaf to the tree scale , 1997 .

[66]  Nigel J. Livingston,et al.  Transfer conductance in second growth Douglas-fir (Pseudotsuga menziesii (Mirb.)Franco) canopies , 2003 .

[67]  W. Bilger,et al.  Chlorophyll fluorescence as a nonintrusive indicator for rapid assessment of in vivo photosynthesis , 1994 .

[68]  Sean C. Thomas,et al.  The worldwide leaf economics spectrum , 2004, Nature.

[69]  J. Čatský Dynamics of Leaf Photosynthesis. Rapid-Response Measurements and Their Interpretations , 1999, Photosynthetica.

[70]  E. Ögren,et al.  Photosynthetic light-response curves , 1993, Planta.

[71]  T. Möls,et al.  Photosynthetic parameters of birch (Betula pendula Roth) leaves growing in normal and in CO2‐ and O3‐ enriched atmospheres , 2004 .

[72]  G. Farquhar,et al.  On the relationship between leaf anatomy and CO2 diffusion through the mesophyll of hypostomatous leaves , 1995 .

[73]  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.

[74]  Nigel J. Livingston,et al.  On the need to incorporate sensitivity to CO2 transfer conductance into the Farquhar–von Caemmerer–Berry leaf photosynthesis model , 2004 .

[75]  J. R. Evans,et al.  The Relationship Between CO2 Transfer Conductance and Leaf Anatomy in Transgenic Tobacco With a Reduced Content of Rubisco , 1994 .

[76]  M. Gullo,et al.  Sclerophylly and plant water relations in three Mediterranean Quercus species. , 1990 .

[77]  X. Le Roux,et al.  Effect of local irradiance on CO(2) transfer conductance of mesophyll in walnut. , 2002, Journal of experimental botany.

[78]  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 .

[79]  M. Adams,et al.  Internal conductance does not scale with photosynthetic capacity: implications for carbon isotope discrimination and the economics of water and nitrogen use in photosynthesis. , 2006, Plant, cell & environment.

[80]  S. Hale,et al.  Comparison of film and digital hemispherical photography across a wide range of canopy densities , 2002 .

[81]  K. Hikosaka,et al.  Leaf anatomy as a constraint for photosynthetic acclimation: differential responses in leaf anatomy to increasing growth irradiance among three deciduous trees , 2005 .

[82]  K. Wilson,et al.  How the environment, canopy structure and canopy physiological functioning influence carbon, water and energy fluxes of a temperate broad-leaved deciduous forest--an assessment with the biophysical model CANOAK. , 2002, Tree physiology.

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

[84]  S. Running,et al.  8 – Generalization of a Forest Ecosystem Process Model for Other Biomes, BIOME-BGC, and an Application for Global-Scale Models , 1993 .

[85]  D. Whitehead,et al.  Corrigendum to: The relative limitation of photosynthesis by mesophyll conductance in co-occurring species in a temperate rainforest dominated by the conifer Dacrydium cupressinum. , 2003, Functional plant biology : FPB.

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

[87]  I. Terashima,et al.  Slow development of leaf photosynthesis in an evergreen broad‐leaved tree, Castanopsis sieboldii: relationships between leaf anatomical characteristics and photosynthetic rate , 2001 .