Temperature response of parameters of a biochemically based model of photosynthesis. I. Seasonal changes in mature maritime pine (Pinus pinaster Ait.)

Responses of plant processes to temperature may vary according to the time scale on which they are measured. In this study, both short-term and seasonal responses of photosynthesis to temperature were examined. A field study of seasonal changes in the temperature response of photosynthesis was conducted on two provenances, French and Moroccan, of mature maritime pine ( Pinus pinaster Ait.). Measurements were made every 2 months over a 1-year period and used to parameterize a mechanistic model of photosynthesis. Temperature responses of maximum Rubisco activity, V cmax , and potential electron transport rate, J max , were obtained for each measurement period, as was the response of stomatal conductance, g s , to water vapour pressure deficit (VPD). Absolute values of V cmax and J max at 25 ° C were related to needle nitrogen content, N area. N area , and thus V cmax and J max , were negatively correlated with the mean minimum temperature in the month preceding measurements. The ratio of J max : V cmax at 25 ° C varied between 1 and 1·7 but did not show any seasonal trend. Nor was there any seasonal trend in the relative temperature response of V cmax , which had an activation energy H a of approximately 57 kJ mol − 1 throughout the experiment. The activation energy of J max was also close to constant throughout the experiment, averaging 39 kJ mol − 1 . For the French provenance, the optimal temperature of J max was positively correlated with the maximum temperature of the previous day, but no such correlation was found for the Moroccan provenance. The response of g s to VPD also varied seasonally, with much stronger stomatal closure in winter months. Taken together, these results implied a translational shift downwards of the photosynthetic temperature response curve with increasing T prev , and a shift in the temperature optimum of photosynthesis of 5‐10 ° C between summer and winter. These results illustrate that the short-term temperature response of photosynthesis varies significantly on a seasonal basis.

[1]  C. Field,et al.  Allocating leaf nitrogen for the maximization of carbon gain: Leaf age as a control on the allocation program , 1983, Oecologia.

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

[3]  J. Bunce,et al.  Acclimation of photosynthesis to temperature in eight cool and warm climate herbaceous C3 species: Temperature dependence of parameters of a biochemical photosynthesis model , 2004, Photosynthesis Research.

[4]  Denis Loustau,et al.  Temperature response of parameters of a biochemically based model of photosynthesis. II. A review of experimental data , 2002 .

[5]  J. Houghton,et al.  Climate change 2001 : the scientific basis , 2001 .

[6]  P. Berbigier,et al.  CO2 and water vapour fluxes for 2 years above Euroflux forest site , 2001 .

[7]  X. Le Roux,et al.  Temperature response of leaf photosynthetic capacity in seedlings from seven temperate tree species. , 2001, Tree physiology.

[8]  Zong-ci Zhao,et al.  Climate change 2001, the scientific basis, chap. 8: model evaluation. Contribution of Working Group I to the Third Assessment Report of the Intergovernmental Panel on Climate Change IPCC , 2001 .

[9]  R. Dewar,et al.  Soil processes dominate the long-term response of forest net primary productivity to increased temperature and atmospheric CO2 concentration. , 2000 .

[10]  D. Ellsworth Seasonal CO(2) assimilation and stomatal limitations in a Pinus taeda canopy. , 2000, Tree physiology.

[11]  A. Kremer,et al.  Provenance hybridization in a diallel mating scheme of maritime pine (Pinus pinaster). I. Means and variance components. , 2000 .

[12]  I. A. Nalder,et al.  Climate change effects on net carbon exchange of a boreal aspen–hazelnut forest: estimates from the ecosystem model ecosys , 2000 .

[13]  R. Norby,et al.  Acclimation of photosynthesis and respiration to simulated climatic warming in northern and southern populations of Acer saccharum: laboratory and field evidence. , 2000, Tree physiology.

[14]  Ü. Niinemets,et al.  Shape of leaf photosynthetic electron transport versus temperature response curve is not constant along canopy light gradients in temperate deciduous trees , 1999 .

[15]  A-M Bosc Etude expérimentale du fonctionnement hydrique et carboné des organes aériens du Pin maritime (Pinus pinaster Ait. ) : intégration dans un modèle structure-fonction appliqué à l'analyse de l'autonomie carbonée des branches de la couronne d'un arbre adulte , 1999 .

[16]  Dennis D. Baldocchi,et al.  On using eco-physiological, micrometeorological and biogeochemical theory to evaluate carbon dioxide, water vapor and trace gas fluxes over vegetation: a perspective , 1998 .

[17]  S. Kellomäki,et al.  Model Computations on the Effects of Elevating Temperature and Atmospheric CO2 on the Regeneration of Scots Pine at the Timber Line in Finland , 1997 .

[18]  K. Hikosaka Modelling Optimal Temperature Acclimation of the Photosynthetic Apparatus in C3Plants with Respect to Nitrogen Use , 1997 .

[19]  R. Leuning Scaling to a common temperature improves the correlation between the photosynthesis parameters Jmax and Vcmax , 1997 .

[20]  J. H. M. Thornley,et al.  Temperate forest responses to carbon dioxide, temperature and nitrogen: a model analysis , 1996 .

[21]  S. Wofsy,et al.  Modelling the soil-plant-atmosphere continuum in a Quercus-Acer stand at Harvard Forest : the regulation of stomatal conductance by light, nitrogen and soil/plant hydraulic properties , 1996 .

[22]  C. Beadle,et al.  Photosynthetic temperature responses of Eucalyptus globulus and Eucalyptus nitens. , 1996, Tree physiology.

[23]  A. Makino,et al.  Effects of Growth Temperature on the Responses of Ribulose-1,5-Biphosphate Carboxylase, Electron Transport Components, and Sucrose Synthesis Enzymes to Leaf Nitrogen in Rice, and Their Relationships to Photosynthesis , 1994, Plant physiology.

[24]  Ross E. McMurtrie,et al.  Mathematical models of the photosynthetic response of tree stands to rising CO2 concentrations and temperatures , 1993 .

[25]  R. Slatyer,et al.  Photosynthetic Temperature Acclimation in Eucalyptus Species From Diverse Habitats, and a Comparison With Nerium oleander , 1989 .

[26]  F. I. Woodward,et al.  Plants and temperature , 1988 .

[27]  W. Inskeep,et al.  Extinction coefficients of chlorophyll a and B in n,n-dimethylformamide and 80% acetone. , 1985, Plant physiology.

[28]  J. Guehl,et al.  Etude comparée des potentialités hivernales d'assimilation carbonée de trois conifères de la zone tempérée (Pseudotsuga menziesii Mirb., Abies alba Mill. et Picea excelsa Link.) , 1985 .

[29]  G. Riechers Plants and Microclimate , 1984 .

[30]  A. Kremer,et al.  Stabilité phénotypique de la croissance en hauteur et cinétique journalière de la pression de sève et de la transpiration chez le pin maritime (Pinuspinaster Ait.) , 1982 .

[31]  J. Berry,et al.  Photosynthetic Response and Adaptation to Temperature in Higher Plants , 1980 .

[32]  U. Schreiber,et al.  Photosynthetic Acclimation to Temperature in the Desert Shrub, Larrea divaricata: II. Light-harvesting Efficiency and Electron Transport. , 1978, Plant physiology.

[33]  Patrick C. Morrow,et al.  Altitudinal Variation in the Photosynthetic Characteristics of Snow Gum, Eucalyptus pauciflora Sieb. Ex Spreng. I. Seasonal Changes Under Field Conditions in the Snowy Mountains Area of South-Eastern Australia , 1977 .

[34]  P. Jarvis,et al.  Photosynthesis in Sitka Spruce (Picea sitchensis (Bong.) Carr.). II. Response to Temperature , 1972 .

[35]  R. A. Webb,et al.  Simultaneous determination of nitrogen, phosphorus and potassium in plant material by automatic methods. , 1970 .