Elevated CO2 and temperature alter nitrogen allocation in Douglas-fir

The effects of elevated CO₂ and temperature on principal carbon constituents (PCC) and C and N allocation between needle, woody (stem and branches) and root tissue of Pseudotsuga menziesii Mirb. Franco seedlings were determined. The seedlings were grown in sun‐lit controlled‐environment chambers that contained a native soil. Chambers were controlled to reproduce ambient or ambient +180 ppm CO₂ and either ambient temperature or ambient +3.5 °C for 4 years. There were no significant CO₂ × temperature interactions; consequently the data are presented for the CO₂ and temperature effects. At the final harvest, elevated CO₂ decreased the nonpolar fraction of the PCC and increased the polar fraction and amount of sugars in the needles. In contrast, elevated temperature increased the nonpolar fraction of the PCC and decreased sugars in needles. There were no CO₂ or temperature effects on the PCC fractions in the woody tissue or root tissue. Elevated CO₂ and temperature had no significant effects on the C content of any of the plant tissues or fractions. In contrast, the foliar N content declined under elevated CO₂ and increased under elevated temperature; there were no significant effects in other tissues. The changes in the foliar N concentrations were in the cellulose and lignin fractions, the fractions, which contain protein, and are the consequences of changes in N allocation under the treatments. These results indicate reallocation of N among plant organs to optimize C assimilation, which is mediated via changes in the selectivity of Rubisco and carbohydrate modulation of gene expression.     

Monoterpene emission from coniferous trees in response to elevated CO2 concentration and climate warming

It was hypothesized that high CO₂ availability would increase monoterpene emission to the atmosphere. This hypothesis was based on resource allocation theory which predicts increased production of plant secondary compounds when carbon is in excess of that required for growth. Monoterpene emission rates were measured from needles of (a) Ponderosa pine grown at different CO₂ concentrations and soil nitrogen levels, and (b) Douglas fir grown at different CO₂ concentrations. Ponderosa pine grown at 700 μmol mol^–1 CO₂ exhibited increased photosynthetic rates and needle starch to nitrogen (N) ratios when compared to trees grown at 350 μmol mol^–1 CO₂. Nitrogen availability had no consistent effect on photosynthesis. Douglas fir grown at 550 μmol mol^–1 CO₂ exhibited increased photosynthetic rates as compared to growth at 350 μmol mol^–1 CO₂ in old, but not young needles, and there was no influence on the starch/N ratio. In neither species was there a significant effect of elevated growth CO₂ on needle monoterpene concentration or emission rate. The influence of climate warming and leaf area index (LAI) on monoterpene emission were also investigated. Douglas fir grown at elevated CO₂ plus a 4 °C increase in growth temperature exhibited no change in needle monoterpene concentration, despite a predicted 50% increase in emission rate. At elevated CO₂ concentration the LAI increased in Ponderosa pine, but not Douglas fir. The combination of increased LAI and climate warming are predicted to cause an 80% increase in monoterpene emissions from Ponderosa pine forests and a 50% increase in emissions from Douglas fir forests. This study demonstrates that although growth at elevated CO₂ may not affect the rate of monoterpene emission per unit biomass, the effect of elevated CO₂ on LAI, and the effect of climate warming on monoterpene biosynthesis and volatilization, could increase canopy monoterpene emission rate.     

Stomatal responses of Douglas-fir seedlings to elevated carbon dioxide and temperature during the third and fourth years of exposure

Two major components of climate change, increasing atmospheric [CO₂] and increasing temperature, may substantially alter the effects of water availability to plants through effects on the rate of water loss from leaves. We examined the interactive effects of elevated [CO₂] and temperature on seasonal patterns of stomatal conductance (g_s), transpiration (E) and instantaneous transpiration efficiency (ITE) in Douglas‐fir (Pseudotsuga menziesii (Mirb.) Franco) seedlings. Seedlings were grown in sunlit chambers at either ambient CO₂ (AC) or ambient + 180 µmol mol^?1 CO₂ (EC), and at ambient temperature (AT) or ambient + 3·5 °C (ET) in a full‐factorial design. Needle gas exchange at the target growth conditions was measured approximately monthly over 21 months. Across the study period and across temperature treatments, growth in elevated [CO₂] decreased E by an average of 12% and increased ITE by an average of 46%. The absolute reduction of E associated with elevated [CO₂] significantly increased with seasonal increases in the needle‐to‐air vapour pressure deficit (D). Across CO₂ treatments, growth in elevated temperature increased E an average of 37%, and did not affect ITE. Combined, growth in elevated [CO₂] and elevated temperature increased E an average of 19% compared with the ACAT treatment. The CO₂ supply and growth temperature did not significantly affect stomatal sensitivity to D or the relationship between g_s and net photosynthetic rates. This study suggests that elevated [CO₂] may not completely ameliorate the effect of elevated temperature on E, and that climate change may substantially alter needle‐level water loss and water use efficiency of Douglas‐fir seedlings.     

Seasonal patterns of photosynthesis in Douglas fir seedlings during the third and fourth year of exposure to elevated CO2 and temperature

The interactive effects of elevated atmospheric CO₂ and temperature on seasonal patterns of photosynthesis in Douglas fir (Psuedotsuga menziesii (Mirb.) Franco) seedlings were examined. Seedlings were grown in sunlit chambers controlled to track either ambient (~400 p.p.m.) CO₂ or ambient +200 p.p.m. CO₂, and either ambient temperature or ambient +4 °C. Light‐saturated net photosynthetic rates were measured approximately monthly over a 21 month period. Elevated CO₂ increased net photosynthetic rates by an average of 21% across temperature treatments during both the 1996 hydrologic year, the third year of exposure, and the 1997 hydrologic year. Elevated mean annual temperature increased net photosynthetic rates by an average of 33% across CO₂ treatments during both years. Seasonal temperature changes also affected net photosynthetic rates. Across treatments, net photosynthetic rates were highest in the spring and autumn, and lowest in July, August and December–January. Seasonal increases in temperature were not correlated with increases in the relative photosynthetic response to elevated CO₂. Seasonal shifts in the photosynthetic temperature optimum reduced temperature effects on the relative response to elevated CO₂. These results suggest that the effects of elevated CO₂ on net photosynthetic rates in Douglas fir are largely independent of temperature.     

Comparison of photosynthetic acclimation to elevated CO2 and limited nitrogen supply in soybean

Plants grown at elevated CO₂ often acclimate such that their photosynthetic capacities are reduced relative to ambient CO₂-grown plants. Reductions in synthesis of photosynthetic enzymes could result either from reduced photosynthetic gene expression or from reduced availability of nitrogen-containing substrates for enzyme synthesis. Increased carbohydrate concentrations resulting from increased photosynthetic carbon fixation at elevated CO₂ concentrations have been suggested to reduce the expression of photosynthetic genes. However, recent studies have also suggested that nitrogen uptake may be depressed by elevated CO₂, or at least that it is not increased enough to keep pace with increased carbohydrate production. This response could induce a nitrogen limitation in elevated-CO₂ plants that might account for the reduction in photosynthetic enzyme synthesis. If CO₂ acclimation were a response to limited nitrogen uptake, the effects of elevated CO₂ and limiting nitrogen supply on photosynthesis and nitrogen allocation should be similar. To test this hypothesis we grew non-nodulating soybeans at two levels each of nitrogen and CO₂ concentration and measured leaf nitrogen contents, photosynthetic capacities and Rubisco contents. Both low nitrogen and elevated CO₂ reduced nitrogen as a percentage of total leaf dry mass but only low nitrogen supply produced significant decreases in nitrogen as a percentage of leaf structural dry mass. The primary effect of elevated CO₂ was to increase non-structural carbohydrate storage rather than to decrease nitrogen content. Both low nitrogen supply and elevated CO₂ also decreased carboxylation capacity (V_cmax) and Rubisco content per unit leaf area. However, when V_cmax and Rubisco content were expressed per unit nitrogen, low nitrogen supply generally caused them to increase whereas elevated CO₂ generally caused them to decrease. Finally, elevated CO₂ significantly increased the ratio of RuBP regeneration capacity to V_cmax whereas neither nitrogen supply nor plant age had a significant effect on this parameter. We conclude that reductions in photosynthetic enzyme synthesis in elevated CO₂ appear not to result from limited nitrogen supply but instead may result from feedback inhibition by increased carbohydrate contents.     

Mathematical models of the photosynthetic response of tree stands to rising CO2 concentrations and temperatures

Two published models of canopy photosynthesis, MAESTRO and BIOMASS, are simulated to examine the response of tree stands to increasing ambient concentrations of carbon dioxide (C_a) and temperatures. The models employ the same equations to described leaf gas exchange, but differ considerably in the level of detail employed to represent canopy structure and radiation environment. Daily rates of canopy photosynthesis simulated by the two models agree to within 10% across a range of CO₂ concentrations and temperatures. A doubling of C_a leads to modest increases of simulated daily canopy photosynthesis at low temperatures (10% increase at 10°C), but larger increases at higher temperatures (60% increase at 30°C). The temperature and CO₂ dependencies of canopy photosynthesis are interpreted in terms of simulated contributions by quantum-saturated and non-saturated foliage. Simulations are presented for periods ranging from a diurnal cycle to several years. Annual canopy photosynthesis simulated by BIOMASS for trees experiencing no water stress is linearly related to simulated annual absorbed photosynthetically active radiation, with light utilization coefficients for carbon of ?= 1.66 and 2.07g MJ^?1 derived for C_a of 350 and 700 μmol mol^?1, respectively.     

Increased photosynthetic capacity of Scirpus olneyi after 4 years of exposure to elevated CO2

Abstract. While a short-term exposure to elevated atmospheric CO₂ induces a large increase in photosynthesis in many plants, long-term growth in elevated CO₂ often results in a smaller increase due to reduced photosynthetic capacity. In this study, it was shown that, for a wild C₃ species growing in its natural environment and exposed to elevated CO₂ for four growing seasons, the photosynthetic capacity has actually increased by 31%. An increase in photosynthetic capacity has been observed in other species growing in the field, which suggests that photosynthesis of certain field grown plants will continue to respond to elevated levels of atmospheric CO₂     

A mechanistic evaluation of photosynthetic acclimation at elevated CO2

Plants grown at elevated pCO₂ often fail to sustain the initial stimulation of net CO₂ uptake rate (A). This reduced, acclimated, stimulation of A often occurs concomitantly with a reduction in the maximum carboxylation velocity (V_c,max) of Rubisco. To investigate this relationship we used the Farquhar model of C₃ photosynthesis to predict the minimum V_c,max capable of supporting the acclimated stimulation in A observed at elevated pCO₂. For a wide range of species grown at elevated pCO₂ under contrasting conditions we found a strong correlation between observed and predicted values of V_c,max. This exercise mechanistically and quantitatively demonstrated that the observed acclimated stimulation of A and the simultaneous decrease in V_c,max observed at elevated pCO₂ is mechanistically consistent. With the exception of plants grown at a high elevated pCO₂ (> 90 Pa), which show evidence of an excess investment in Rubisco, the failure to maintain the initial stimulation of A is almost entirely attributable to the decrease in V_c,max and investment in Rubisco is coupled to requirements.     

Nonlinearity of photosynthetic responses to growth in rising atmospheric CO2: an experimental and modelling study

Nonlinear responses of photosynthesis to the CO₂ concentration at which plants were grown (C_g) have been often reported in the literature. This study was designed to develop mechanistic understanding of the nonlinear responses with both experimental and modelling approaches. Soybean (Glycine max) was grown in five levels of C_g (280, 350, 525, 700, 1000 ppm) with either a high or low rate of nitrogen fertilization. When the rate of nitrogen fertilization was high, the photosynthetic rate measured at C_g was highest in plants from the 700 ppm CO₂ treatment. When the rate of nitrogen fertilization was low, little variation was observed in the photosynthetic rates of plants from the different treatments measured at their respective C_g. Measurements of CO₂-induced changes in mass-based leaf nitrogen concentration (n_m, an index of changes in biochemical processes) and leaf mass per unit area (h, an index of morphological properties) were used in a model and indicate that the nonlinearity of photosynthetic responses to C_g is largely determined by relative changes in photosynthetic sensitivity, biochemical downregulation, and morphological upregulation. In order to further understand the nonlinear responses, we compiled data from the literature on CO₂-induced changes in n_m and h. These compiled data indicate that h generally increases and n_m usually decreases with increasing C_g, but that the trajectories and magnitudes of the changes in h and n_m vary with species and growth environments. Integration of these variables (n_m and h) into a biochemically based model of photosynthesis enabled us to predict diverse responses of photosynthesis to C_g. Thus a general mechanism is suggested for the highly variable, nonlinear responses of photosynthesis to C_g reported in the literature.     

Simple carbon assimilation response functions from atmospheric CO2, and daily temperature and shortwave radiation

A global ‘CO₂ fertilizer effect’ multiplier is often used in crop or ecosystem models because of its simplicity. However, this approach does not take into account the interaction between CO₂, temperature and light on assimilation. This omission can lead to significant under- or overestimation of the magnitude of beneficial effects from elevated CO₂, depending on environmental conditions. We use a mechanistic model of the biochemistry of photosynthesis to represent the response of net assimilation to different levels of CO₂, temperature and radiation, on the daily time scale. Instantaneous assimilation rates for an idealized canopy model are integrated through diurnal cycles of environmental variables derived from historical climate data at three locations in North America. The calculated CO₂ fertilizer effect is greatest at high light and warm temperatures. The results are summarized by assimilation response surfaces specified by the CO₂ concentration, the canopy leaf area index, and by daily values of temperature and radiation available from climatic records. These summary functions are suitable for incorporation into crop or ecosystem models for predicting carbon assimilation or biomass production on a daily time step. An example application of the function reveals that for a relatively cool, high latitude location, the beneficial effects from a CO₂ doubling would be negligible during the early spring, even assuming a + 4°C global warming scenario. In contrast, the beneficial effects from increasing CO₂ at a relatively warm, lower latitude location are greatest in the spring, but decline in late summer because of excessively warm temperatures with a + 4°C global warming.     

Variable photosynthetic acclimation in consecutive cohorts of Scots pine needles during 3 years of growth at elevated CO2 and elevated temperature

In this experiment, the photosynthetic acclimation of successive needle cohorts of Scots pine were studied during 3 years of growth at elevated CO₂ and temperature. Naturally regenerated Scots pine (Pinus sylvestris L.) trees were subjected to elevated CO₂ concentration (+CO₂, 700 p.p.m), elevated temperature (+T, ambient +2 to +6 °C) and to a combination of elevated CO₂ and temperature (+CO₂ + T) in closed‐top chambers, starting in August 1996. Trees growing in chambers with ambient CO₂ and ambient temperature served as controls (AmbC). Elevated CO₂ influenced the dark reactions more than the light reactions of photosynthesis, as in the 1996 and 1997 cohorts the carboxylation capacity of Rubisco was reduced in the first and second year of exposure, but there was no consistent change in chlorophyll fluorescence. Net photosynthesis measured at growth concentration of CO₂ was higher at +CO₂ than at AmbC on only one measuring occasion, was generally lower at +T and was not changed at +CO₂ + T. However, trees grown at +T tended to invest more nitrogen (N) in Rubisco, as Rubisco/chlorophyll and the proportion of the total needle N bound to Rubisco occasionally increased. The interaction of +CO₂ and +T on Rubisco was mostly negative; consequently, in the second and third year of the experiment the carboxylation capacity decreased at +CO₂ + T. In the 1996, 1997 and 1998 cohorts, the structural N concentration of needles was lower at +CO₂ than at AmbC. Elevated CO₂ and elevated temperature generally had a positive interaction on N concentration; consequently, N concentration in needles decreased less at +CO₂ + T than at +CO₂. At +CO₂ + T, the acclimation response of needles varied between years and was more pronounced in the 1‐year‐old needles of the 1997 cohort than in those of the 1998 cohort. Thus, acclimation was not always greater in 1‐year‐old needles than in current‐year needles. In the +CO₂ + T treatment, elevated temperature had a greater effect on acclimation of needles than elevated CO₂.     

A search for predictive understanding of plant responses to elevated [CO2]

This paper reviews two decades of effort by the scientific community in a search for predictive understanding of plant responses to elevated [CO₂]. To evaluate the progress of research in leaf photosynthesis, plant respiration, root nutrient uptake, and carbon partitioning, we divided scientific activities into four phases: (I) initial assessments derived from our existing knowledge base to provide frameworks for experimental studies; (II) experimental tests of the initial assessments; (III) in cases where assessments were invalidated, synthesis of experimental results to stimulate alternative hypotheses and further experimentation; and (IV) formation of new knowledge. This paper suggests that photosynthetic research may have gone through all four phases, considering that (a) variable responses of photosynthesis to [CO₂] are generally explainable, (b) extrapolation of leaf-level studies to the global scale has been examined, and (c) molecular studies are under way. Investigation of plant respiratory responses to [CO₂] has reached the third phase: experimental results have been accumulated, and mechanistic approaches are being developed to examine alternative hypotheses in search for new concepts and/or new quantitative frameworks to understand respiratory responses to elevated [CO₂]. The study of nutrient uptake kinetics is still in the second phase: experimental evidence has contradicted some of the initial assessments, and more experimental studies need to be designed before generalizations can be made. It is quite unfortunate that we have not made much progress in understanding mechanisms of carbon partitioning during the past two decades. This is due in part to the fact that some of the holistic theories, such as functional balance and optimality, have not evolved into testable hypotheses to guide experimental studies. This paper urges modelers to play an increasing role in plant–CO₂ research by disassembling these existing theories into hypotheses and urges experimentalists to design experiments to examine these holistic concepts.     

Potential effects of elevated CO2 and changes in temperature on tropical plants

Abstract. Very little attention has been directed at the responses of tropical plants to increases in global atmospheric CO₂ concentrations and the potential climatic changes. The available data, from greenhouse and laboratory studies, indicate that the photosynthesis, growth and water use efficiency of tropical plants can increase at higher CO₂ concentrations. However, under field conditions abiotic (light, water or nutrients) or biotic (competition or herbivory) factors might limit these responses. In general, elevated atmospheric CO₂ concentrations seem to increase plant tolerance to stress, including low water availability, high or low temperature, and photoinhibition. Thus, some species may be able to extend their ranges into physically less favourable sites, and biological interactions may become relatively more important in determining the distribution and abundance of species. Tropical plants may be more narrowly adapted to prevailing temperature regimes than are temperate plants, so expected changes in temperature might be relatively more important in the tropics. Reduced transpiration due to decreased stomatal conductance could modify the effects of water stress as a cue for vegetative or reproductive phenology of plants of seasonal tropical areas. The available information suggests that changes in atmospheric CO₂ concentrations could affect processes as varied as plant/herbivore interactions, decomposition and nutrient cycling, local and geographic distributions of species and community types, and ecosystem productivity. However, data on tropical plants are few, and there seem to be no published tropical studies carried out in the field. Immediate steps should be undertaken to reduce our ignorance of this critical area.     

The sensitivity of C3 photosynthesis to increasing CO2 concentration: a theoretical analysis of its dependence on temperature and background CO2 concentration

The atmospheric CO₂ concentration has increased from the pre-industrial concentration of about 280 μmol mol⁻¹ to its present concentration of over 350 μmol mol⁻¹, and continues to increase. As the rate of photosynthesis in C₃ plants is strongly dependent on CO₂ concentration, this should have a marked effect on photosynthesis, and hence on plant growth and productivity. The magnitude of photo-synthetic responses can be calculated based on the well-developed theory of photosynthetic response to intercellular CO₂ concentration. A simple biochemically based model of photosynthesis was coupled to a model of stomatal conductance to calculate photosynthetic responses to ambient CO₂ concentration. In the combined model, photosynthesis was much more responsive to CO₂ at high than at low temperatures. At 350 μmol mol⁻¹, photosynthesis at 35°C reached 51% of the rate that would have been possible with non-limiting CO₂, whereas at 5°C, 77% of the CO₂ non-limited rate was attained. Relative CO₂ sensitivity also became smaller at elevated CO₂, as CO₂ concentration increased towards saturation. As photosynthesis was far from being saturated at the current ambient CO₂ concentration, considerable further gains in photosynthesis were predicted through continuing increases in CO₂ concentration. The strong interaction with temperature also leads to photosynthesis in different global regions experiencing very different sensitivities to increasing CO₂ concentrations.     

Simulated influence of altitude on photosynthetic CO2 uptake potential in plants

Abstract. A simulation of the quantitative influence of altitude on photosynthetic CO₂ uptake capability (A^P) included the effects of predicted changes (1) in air temperature (lapse rate) and (2) leaf temperature, (3) ambient pressure and CO₂ concentration, and (4) the diffusion coefficient for CO² in air. When a dry lapse rate (0.01°C m⁻¹) in air temperature was simulated, significant declines (up to 14%) in A^P were predicted from sea level to 4km altitude. A moist lapse rate of 0.003°C m⁻¹ resulted in less than a 4% decrease in A^P over the same altitude range. When natural leaf temperatures (predicted from heat balance analyses) were simulated, A^P was significantly greater (∼20%) than when leaf temperatures were considered equal to air temperature for all lapse conditions. There was virtually no change in A^P with altitude when predicted leaf temperatures and moist lapse conditions were simulated. There was a significant (∼10%) increase in A^P with altitude when leaf temperature was held constant at 30°C (regardless of altitude) under moist lapse conditions. Future studies evaluating the effects of elevation on photosynthesis could benefit from the above considerations of the effects of natural leaf temperature regimes and prevailing lapse conditions on CO₂ uptake potential.     

Aphid individual performance may not predict population responses to elevated CO2 or O3

Changes in atmospheric composition affect plant quality and herbivore performance. We used the Aspen Free Air CO₂ Enrichment (FACE) facility to investigate the impacts of elevated carbon dioxide (CO₂) and ozone (O₃) on the performance of the aphid Cepegillettea betulaefoliae Granovsky feeding on paper birch (Betula papyrifera Marsh.). In Year 1, we simultaneously measured individual performance and population growth rates, and in Year 2 we surveyed natural aphid, predator and parasitoid populations throughout the growing season. Aphid growth and development (relative growth rate (RGR), development time, adult weight, embryo number and the birth weight of newborn nymphs) were unaffected by CO₂ and O₃. Aphid fecundity decreased on trees grown at elevated CO₂, O₃ and CO₂+O₃. Neither nymphal performance nor adult size were reliable indicators of future fecundity at elevated CO₂ and/or O₃. Aphid populations protected from natural enemies were unaffected by elevated CO₂, but increased significantly at elevated O₃. Individual fecundity in elevated CO₂ and O₃ atmospheres did not predict population growth rates, probably because of changes in the strength of intraspecific competition or the ability of the aphids to induce nutrient sinks. Natural aphid, predator and parasitoids populations (Year 2) showed few significant responses to CO₂ and O₃, although CO₂ and O₃ did affect the timing of aphid and natural enemy peak abundance. Elevated CO₂ and O₃ affected aphid and natural enemy populations independently: no CO₂× O₃ interactions were observed. We conclude that: (1) aphid individual performance did not predict population responses to CO₂ and O₃ and (2) elevated CO₂ and O₃ atmospheres are unlikely to affect C. betulaefoliae populations in the presence of natural enemy communities.