GROSS PRIMARY PRODUCTIVITY IN DUKE FOREST: MODELING SYNTHESIS OF CO2 EXPERIMENT AND EDDY -FLUX DATA

This study was designed to estimate gross primary productivity (GPP) in the Duke Forest at both ambient and elevated CO2 (ambient + 200 fLL/L) concentrations using a physiologically based canopy model. The model stratified the canopy of loblolly pine (Pinus taeda L.) forest into six layers and estimated photosynthesis in each layer according to the Farquhar sub model coupled with the Ball-Berry stomatal conductance sub model. The model was parameterized with a suite of physiological measurements, in- cluding leaf area index (LAI), leaf nitrogen (N) concentration, photosynthesis-N relation- ships, and stomatal conductance. The model was validated against measured leaf photo- synthesis and canopy carbon (C) fluxes estimated from eddy-covariance measurements (ECM). Application of this model to simulate canopy C fixation from 28 August 1996, the onset of CO2 fumigation, to 31 December 1998 suggested that elevation of atmospheric (CO2J to ambient + 200 fLL/L resulted in increase of canopy C fixation by 35% in 1996, 39% in 1997, and 43% in 1998. The modeled GPP and its response to elevated (CO2J were sensitive to parameter values of quantum yield of electron transport, leaf area index, and the vertical distribution of LAI within the canopy. Thus, further investigation on those parameters will help improve the precision of estimated ecosystem-scale C fluxes. Fur- thermore, comparison between the modeled and ECM-estimated canopy C fluxes suggested that soil moisture, in addition to air vapor pressure, controlled canopy photosynthesis during the drought period.

[1]  Boyd R. Strain,et al.  Direct effects of increasing carbon dioxide on vegetation , 1985 .

[2]  I. E. Woodrow,et al.  A Model Predicting Stomatal Conductance and its Contribution to the Control of Photosynthesis under Different Environmental Conditions , 1987 .

[3]  B. Bugbee Steady-state canopy gas exchange: system design and operation. , 1992, HortScience : a publication of the American Society for Horticultural Science.

[4]  D. Whitehead,et al.  The response of photosynthetic model parameters to temperature and nitrogen concentration in Pinus radiata D. Don , 1997 .

[5]  E. DeLucia,et al.  Photosynthetic capacity of loblolly pine (Pinus taeda L.) trees during the first year of carbon dioxide enrichment in a forest ecosystem , 1999 .

[6]  G. Katul,et al.  Modeling CO2 sources, sinks, and fluxes within a forest canopy , 1999 .

[7]  Y. P. Wang,et al.  Two-dimensional needle-area density distribution within the crowns of Pinus radiata. , 1990 .

[8]  R. Whittaker Communities and Ecosystems , 1975 .

[9]  Paul G. Jarvis,et al.  Mean leaf angles for the ellipsoidal inclination angle distribution , 1988 .

[10]  J. Tenhunen,et al.  Modeling the effects of elevated CO2 on plants: extrapolating leaf response to a canopy , 1992 .

[11]  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 .

[12]  Baker,et al.  Does free-Air carbon dioxide enrichment affect photochemical energy use by evergreen trees in different Seasons? A chlorophyll fluorescence study of mature loblolly pine , 1999, Plant physiology.

[13]  James F. Reynolds,et al.  VALIDITY OF EXTRAPOLATING FIELD CO2 EXPERIMENTS TO PREDICT CARBON SEQUESTRATION IN NATURAL ECOSYSTEMS , 1999 .

[14]  P. De Angelis,et al.  Effects of elevated (CO2) on photosynthesis in European forest species: a meta-analysis of model parameters , 1999 .

[15]  G. Katul,et al.  WATER BALANCE DELINEATES THE SOIL LAYER IN WHICH MOISTURE AFFECTS CANOPY CONDUCTANCE , 1998 .

[16]  John M. Norman,et al.  4 – Scaling Processes between Leaf and Canopy Levels , 1993 .

[17]  Edward B. Rastetter,et al.  RESPONSES OF N‐LIMITED ECOSYSTEMS TO INCREASED CO2: A BALANCED‐NUTRITION, COUPLED‐ELEMENT‐CYCLES MODEL , 1997 .

[18]  D. Sims,et al.  Elevated CO2 concentration has independent effects on expansion rates and thickness of soybean leaves across light and nitrogen gradients , 1998 .

[19]  D. Sims,et al.  Nonlinearity of photosynthetic responses to growth in rising atmospheric CO2: an experimental and modelling study , 1998 .

[20]  Finzi,et al.  Net primary production of a forest ecosystem with experimental CO2 enrichment , 1999, Science.

[21]  E. Rastetter,et al.  PREDICTING GROSS PRIMARY PRODUCTIVITY IN TERRESTRIAL ECOSYSTEMS , 1997 .

[22]  Lianhai Wu,et al.  ELEVATED CO2 DIFFERENTIATES ECOSYSTEM CARBON PROCESSES: DECONVOLUTION ANALYSIS OF DUKE FOREST FACE DATA , 2001 .

[23]  Steven G. McNulty,et al.  Loblolly pine hydrology and productivity across the southern United States , 1996 .

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

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

[26]  E. Rastetter,et al.  Seasonal variation in net carbon exchange and evapotranspiration in a Brazilian rain forest: a modelling analysis , 1998 .

[27]  Stan D. Wullschleger,et al.  Biochemical Limitations to Carbon Assimilation in C3 Plants—A Retrospective Analysis of the A/Ci Curves from 109 Species , 1993 .

[28]  Paul G. Jarvis,et al.  Description and validation of an array model - MAESTRO. , 1990 .

[29]  J. Coleman,et al.  Photosynthetic down-regulation in Larrea tridentata exposed to elevated atmospheric CO2: Interaction with drought under glasshouse and field (FACE) exposure , 1998 .

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

[31]  T. C. Hennessey,et al.  Physiology and genetics of tree growth response to moisture and temperature stress: an examination of the characteristics of loblolly pine (Pinus taeda L.). , 1987, Tree physiology.

[32]  Christopher B. Field,et al.  Predicting responses of photosynthesis and root fraction to elevated [CO2]a: interactions among carbon, nitrogen, and growth* , 1994 .

[33]  R. McMurtrie,et al.  Long-Term Response of Nutrient-Limited Forests to CO"2 Enrichment; Equilibrium Behavior of Plant-Soil Models. , 1993, Ecological applications : a publication of the Ecological Society of America.

[34]  Christopher B. Field,et al.  The Terrestrial Carbon Cycle: Implications for the Kyoto Protocol , 1998, Science.

[35]  J. Nagy,et al.  A free‐air enrichment system for exposing tall forest vegetation to elevated atmospheric CO2 , 1999 .

[36]  J. Coleman,et al.  Canopy quantum yield in a mesocosm study , 2000 .

[37]  C. Field,et al.  The photosynthesis - leaf nitrogen relationship at ambient and elevated atmospheric carbon dioxide: a meta-analysis , 1998 .

[38]  P. Jarvis,et al.  Carbon balance of young birch trees grown in ambient and elevated atmospheric CO2 concentrations , 1998 .

[39]  D. Jordan,et al.  The CO2/O 2 specificity of ribulose 1,5-bisphosphate carboxylase/oxygenase : Dependence on ribulosebisphosphate concentration, pH and temperature. , 1984, Planta.

[40]  D. Sims,et al.  Photosynthetic acclimation to elevated CO2 in a sunflower canopy , 1999 .

[41]  Stephen P. Long,et al.  Modification of the response of photosynthetic productivity to rising temperature by atmospheric CO2 concentrations: Has its importance been underestimated? , 1991 .

[42]  R. Leuning A critical appraisal of a combined stomatal‐photosynthesis model for C3 plants , 1995 .

[43]  D. Ellsworth CO2 enrichment in a maturing pine forest: are CO2 exchange and water status in the canopy affected? , 1999 .