Search

Elevated CO2 and warmer temperatures represent the future environmental conditions in the context of global change. A good understanding of plant response to their combined effects is, therefore, critically important for predicting future plant performance. This study investigated the photosynthetic acclimation of Amur linden (Tilia amurensis) seedlings (current year, about 60 cm tall), a shade-tolerant tree species in the temperate broadleaf deciduous forest, to the combination of current CO2 concentration and temperature (CC) and the combination of the predicted future CO2 concentration and temperature (FC). The results show that FC promoted aboveground growth, but reduced photosynthetic capacity (V cmax: maximum rate of RuBP carboxylation and J max: maximum photosynthetic electron transport rate). However, the photosynthetic rate measured under the corresponding growth CO2 concentration was still higher under FC than under CC. FC depressed the photosynthetic limiting transition point (C i-t, A n-t) from Rubisco carboxylation to RuBP regeneration, i.e. A n-t decreased without a change in C i-t. FC did not change leaf N concentration but increased the total leaf N content per tree and photosynthetic nitrogen utilization efficiency. This suggests that N utilization, rather than photosynthetic capacity, may play an important role in the acclimation of the species to future climatic conditions. This study provides new insights into the photosynthetic acclimation of Amur linden and can be used to predict its possible performance under future climatic conditions. [ABSTRACT FROM AUTHOR]

Elevated CO2 and warmer temperature occur simultaneously under the current climate change. However, their combined effects on the photosynthetic traits in boreal trees are not well understood. This study investigated the morphological and photosynthetic responses of yellow birch (Betula alleghaniensis Britt.) to a combined treatment of CO2 and temperature (ambient, ACT (400 μmol mol−1 CO2 and current temperature) vs elevated, ECT (750 μmol mol−1 CO2 and current +4 °C temperature)). It was found that ECT significantly reduced leaf-area based photosynthetic rate (A n ), maximum Rubisco carboxylation rate (V c max), photosynthetic electron transport rate (J max), leaf nitrogen concentration, respiration and mesophyll conductance. There were two interesting findings: first, the primary mechanism of photosynthetic limitation shifted from Ribulose-1,5-bisphosphate (RuBP) carboxylation (related to V c max) to RuBP regeneration (related to J max) in response to ECT, leading to decreased transition point (C i-t and A n-t ) from RuBP carboxylation to regeneration; second, the increase in total leaf area in response to ECT more than compensated for the downregulation of leaf-area based photosynthesis, leading to greater biomass in ECT than in ACT. We proposed a new protocol for evaluating photosynthetic limitations by comparing the relative relationship between the transition point (C i-t and A n-t ) and the photosynthetic rate at growth CO2 (C i-g and A n-g ). Furthermore, we found that J max (RuBP regeneration) was the primary limitation to A n under ECT. [ABSTRACT FROM AUTHOR]

Aims Black spruce (Picea mariana [Mill.] B.S.P.) and white spruce (Picea glauca [Moench] Voss.) are congeneric species. Both are moderately shade tolerant and widely distributed across North American boreal forests. Methods To understand light effects on their ecophysiological responses to elevated CO2, 1-year-old seedlings were exposed to 360 µmol mol−1 and 720 µmol mol−1 CO2 at three light conditions (100%, 50% and 30% of full light in the greenhouse). Foliar gas exchanges were measured in the mid- and late-growing season. Important Findings Elevated CO2 increased net photosynthesis (P n) and photosynthetic water use efficiency, but it reduced stomatal conductance and transpiration. The stimulation of photosynthesis by elevated CO2 was greatest at 50% light and smallest at 100%. Photosynthesis, maximum carboxylation rate (V cmax) and light-saturated rate of electron transport (J max) all decreased with decreasing light. Elevated CO2 significantly reduced V cmax across all light treatments and both species in mid-growing season. However, the effect of elevated CO2 became insignificant at 30% light later in the growing season, with the response being greater in black spruce than in white spruce. Elevated CO2 also reduced J max in white spruce in both measurements while the effect became insignificant at 30% light later in the growing season. However, the effect on black spruce varied with time. Elevated CO2 reduced J max in black spruce in mid-growing season in all light treatments and the effect became insignificant at 30% light later in the growing season, while it increased J max later in the season at 100% and 50% light. These results suggest that both species benefited from elevated CO2, and that the responses varied with light supply, such that the response was primarily physiological at 100% and 50% light, while it was primarily morphological at 30% light. [ABSTRACT FROM AUTHOR]

Past research suggests climate change will cause the climate envelopes of various tree species to shift to higher latitudes and can lead to a northward migration of trees. However, the success and scope of the migration are likely affected by factors that are not contained in the climate envelope, such as photoperiod and interactive effects of multiple environmental factors, and these effects are currently not well understood. In this study, we investigated the interactive effects of CO2 concentrations ([CO2]), photoperiod and soil moisture on the morphological and physiological traits of Populus tremuloides Michx. We grew seedlings under two levels of [CO2] (ambient [CO2] (AC) 400 vs elevated [CO2] (EC) 1000 μmol mol−1), four photoperiod regimes (growing season photoperiods at 48 (seed origin), 52, 55 and 58°N latitude) and two soil moisture regimes (high soil moisture (HSM) vs low soil moisture (LSM), −2 MPa) for two growing seasons in greenhouses. Both morphological and physiological responses were observed. Low soil moisture reduced leaf size, total leaf area and height growth by 33, 46 and 12%, respectively, and increased root/shoot ratio by 20%. The smaller leaf area and increased root/shoot ratio allowed the seedlings in LSM to maintain higher the maximum rate of Rubisco carboxylation (V cmax) and the maximum rate of electron transport for RuBP regeneration (J max) than control seedlings (55 and 83% higher in July, 52 and 70% in August, respectively). Photoperiod and [CO2] modified responses to LSM and LSM altered responses to photoperiod and [CO2], e.g. the August photosynthetic rate was 44% higher in LSM than in HSM under EC but no such a difference existed under AC. The increase in V cmax and J max in response to LSM varied with photoperiod (V cmax: 36% at 52°N, 22% at 55°N, 47% at 58°N; J max: 29% at 52°N, 21% at 55°N, 45% at 58°N). Stomatal conductance and its reduction in response to LSM declined with increasing photoperiod, which can have significant implications for soil moisture effect on northward migration. This study highlights the need to consider the complex interactions of [CO2], photoperiod and soil moisture when planning assisted migration or predicting the natural migration of boreal forests in the future. [ABSTRACT FROM AUTHOR]

The distribution of tree species is expected to shift toward the pole in response to the climate change associated with the elevation of atmospheric CO2 concentration [CO2]. The shift will expose trees to a new photoperiod regime and other environmental conditions. The changes in these factors will likely have interactive effects on the ecophysiological traits of plants. This study investigated how CO2 elevation and change in photoperiod influence the timing of bud development, leaf senescence, and cold hardiness in the fall, and bud break in the spring in boreal white birch (Betula papyrifera Marsh.). Seedlings were exposed to two different [CO2] (AC = 400 μmol mol–1; EC = 1000 μmol mol–1) and four simulated photoperiod regimes in the greenhouse corresponding to each latitude [48 (seed origin), 52, 55, and 58°N] for two growing seasons. We found that EC advanced the initiation of leaf color change (10% leaf color change) in the fall by 23 days, but delayed the completion date of color change (90%). Leaf senescence started earlier in the photoperiods corresponding to 55 and 58°N latitude than those at 48 and 52°N latitudes under EC, but photoperiod did not affect leaf senescence under AC. Additionally, the temperature causing 50% electrolyte leakage (a measure of susceptibility to freezing damage) was more negative under the photoperiod corresponding to 55° (−46°C) and at 58°N (−60°C) under EC than at the lower latitudes (above −40°C). Budburst in the spring occurred earlier under the photoperiods corresponding to the two highest latitudes under EC, but the trend was opposite under AC. The combination of longer photoperiods and elevated [CO2] resulted in earlier budburst in the spring and later completion of leaf senescence in the fall as well as greater cold hardiness, leading to extended growing seasons from both ends. However, the onset of leaf senescence was earlier than in other treatment combinations. Furthermore, the photoperiod effects were quite different under the ambient [CO2]. Our results suggest that it is extremely important to consider the complex interactions of [CO2] and photoperiod in planning latitudinal seed transfers and in predicting the migration of boreal trees in response to climate change. [ABSTRACT FROM AUTHOR]

Global climate change is expected to affect how plants respond to their physical and biological environments. In this study, we examined the effects of elevated CO2 ([CO2]) and low soil moisture on the physiological responses of mountain maple (Acer spicatum L.) seedlings to light availability. The seedlings were grown at ambient (392 µmol mol−1) and elevated (784 µmol mol−1) [CO2], low and high soil moisture (M) regimes, at high light (100%) and low light (30%) in the greenhouse for one growing season. We measured net photosynthesis (A), stomatal conductance (gs), instantaneous water use efficiency (IWUE), maximum rate of carboxylation (Vcmax), rate of photosynthetic electron transport (J), triose phosphate utilization (TPU)), leaf respiration (Rd), light compensation point (LCP) and mid-day shoot water potential (Ψx). A and gs did not show significant responses to light treatment in seedlings grown at low soil moisture treatment, but the high light significantly decreased the Ci/Ca in those seedlings. IWUE was significantly higher in the elevated compared with the ambient [CO2], and the effect was greater at high than the low light treatment. LCP did not respond to the soil moisture treatments when seedlings were grown in high light under both [CO2]. The low soil moisture significantly reduced Ψx but had no significant effect on the responses of other physiological traits to light or [CO2]. These results suggest that as the atmospheric [CO2] rises, the physiological performance of mountain maple seedlings in high light environments may be enhanced, particularly when soil moisture conditions are favourable. [ABSTRACT FROM AUTHOR]

Northern white-cedar (Thuja occidentalis L.) regeneration originating from layering is generally considered to be more shade tolerant than that of seed origin. In this study, we examined photosynthetic light-use efficiency, an important component of shade tolerance, of these two forms of regeneration using light-response curves of 1-year-old rooted cuttings of layers and seedlings grown under low (20% of full sun) and high (>90% of full sun) light conditions Northern white-cedar showed a strong potential for photosynthetic acclimation to light availability, as indicated by significant differences in the light compensation point (LCP), dark respiration (Rd), apparent quantum efficiency (PE), and light saturation point (Qsat) but not light-saturated rate of net photosynthesis (Amax) between cuttings grown under high and low light. Values of LCP, and PE did not differ between layers and seedlings grown under high and low light, but layers had higher Amax and Qsat than seedlings when grown under high light. This result may reflect a comparatively lower capacity for photosynthetic acclimation of seedlings to high light conditions, perhaps because of their younger physiological age. A lower capacity for photosynthetic acclimation to light in seedlings could limit the repair and recovery of their photosynthetic systems from damage associated with the more extreme microenvironments of open, recently disturbed sites. [ABSTRACT FROM AUTHOR]

To investigate the interactive effects of atmospheric carbon dioxide concentration ([CO2]) and nutrition on photosynthesis and its acclimation to elevated [CO2], a two-way factorial experiment was carried out with two nutritional regimes (high- and low-nitrogen (N), phosphorus (P) and potassium (K)) and two CO2 concentrations (360 and 720 ppm) with white birch seedlings (Betula papyrifera Marsh.) grown for four months in environment-controlled greenhouses. Elevated [CO2] enhanced maximal carboxylation rate (Vcmax), photosynthetically active radiation-saturated electron transport rate (Jmax), actual photochemical efficiency of photosystem II (PSII) in the light (ΔF/Fm′) and photosynthetic linear electron transport to carboxylation (Jc) after 2.5 months of treatment, and it increased net photosynthetic rate (An), photosynthetic water-use efficiency (WUE), photosynthetic nitrogen-use efficiency (NUE) and photosynthetic phosphorus-use efficiency (PUE) after 2.5 and 3.5 months of treatment, but it reduced stomatal conductance (gs), transpiration rate (E) and the fraction of total photosynthetic linear electron transport partitioned to oxygenation (Jo/JT) after 2.5 and 3.5 months of treatment. Low nutrient availability decreased An, WUE, Vcmax, Jmax, triose phosphate utilization (TPU), (/Fm′ – F)//Fm′ and Jc, but increased Jo/JT and NUE. Generally, Vcmax was more sensitive to nutrient availability than Jmax. There were significant interactive effects of [CO2] and nutrition over time, e.g., the positive effects of high nutrition on An, Vcmax, Jmax, ΔF/Fm′ and Jc were significantly greater in elevated [CO2] than in ambient [CO2]. In contrast, the interactive effect of [CO2] and nutrition on NUE was significant after 2.5 months of treatment, but not after 3.5 months. High nutrient availability generally increased PUE after 3.5 months of treatment. There was evidence for photosynthetic up-regulation in response to elevated [CO2], particularly in seedlings receiving high nutrition. Photosynthetic depression in response to low nutrient availability was attributed to biochemical limitation (or increased mesophyll resistance) rather than stomatal limitation. Elevated [CO2] reduced leaf N concentration, particularly in seedlings receiving low nutrition, but had no significant effect on leaf P or K concentration. High nutrient availability generally increased area-based leaf N, P and K concentrations, but had negligible effects on K after 2.5 months of treatment. [ABSTRACT FROM AUTHOR]

One-year-old jack pine (Pinus banksiana Lamb.) and current-year white birch (Betula papyrifera Marsh.) seedlings were grown in ambient (360 ppm) or twice ambient (720 ppm) atmospheric CO2 concentration ([CO2]) and at three soil temperatures (Tsoil = 7, 17 and 27 °C initially, increased to 10, 20 and 30 °C two months later, respectively) in a greenhouse for 4 months. In situ foliar gas exchange, in vivo carboxylation characteristics and chlorophyll fluorescence were measured after 2.5 and 4 months of treatment. Low Tsoil suppressed net photosynthetic rate (Pn), stomatal conductance (gs) and transpiration rate (E) in jack pine in both CO2 treatments and gs and E in white birch in ambient [CO2], but enhanced instantaneous water-use efficiency (IWUE) in both species after 2.5 months of treatment. Treatment effects on gs and E remained significant throughout the 4-month study. Low Tsoil reduced maximal carboxylation rate (Vcmax) and PAR-saturated electron transport rate (Jmax) in jack pine in elevated [CO2] after 2.5 months of treatment, but not after 4 months of treatment. Low Tsoil increased actual photochemical efficiency of photosystem II (PSII) in the light (ΔF/Fm′) in jack pine, but decreased ΔF/Fm′ in white birch after 4 months of treatment. In response to low Tsoil, photosynthetic linear electron transport to carboxylation (Jc) decreased in jack pine after 2.5 months and in white birch after 4 months of treatment. Low Tsoil increased the ratio of the photosynthetic linear electron transport to oxygenation (Jo) to the total photosynthetic linear electron transport rate through PSII (Jo/JT) in both species after 2.5 months of treatment, but the effects became statistically insignificant in white birch after 4 months of treatment. High Tsoil decreased foliar N concentration in white birch. Elevated [CO2] increased Pn, IWUE and Jc but decreased Jo/JT in both species at both measurement times except Jc in white birch after 2.5 months of treatment. Elevated [CO2] also decreased gs and E in white birch at high Tsoil, Vcmax in both species and triose phosphate utilization in white birch at low Tsoil after 4 months of treatment, and ΔF/Fm′ in white birch after 2.5 months of treatment. Elevated [CO2] also increased foliar N concentration in both species. Low Tsoil caused no permanent damage to PSII in either species, but jack pine responded and acclimated to low Tsoil more quickly than white birch. Photosynthetic down-regulation and a decrease in photosynthetic electron transport to photorespiration occurred in both species in response to elevated [CO2]. [ABSTRACT FROM AUTHOR]

To examine the effects of soil temperature on a coupled photosynthesis–stomatal conductance model, seedlings of trembling aspen (Populus tremuloides Michx.), jack pine (Pinus banksiana Lamb.), black spruce (Picea Mariana (Mill.) B.S.P.) and white spruce (Picea glauca (Moench) Voss) were exposed to soil temperatures ranging from 5 to 35 °C for 4 months. Light and CO2 response curves of foliar gas exchange were measured for model parameterization. The effects of soil temperature on four key model parameters, Vcmax (maximum rate of carboxylation), Jmax (maximum rate of electron transport), α (energy conversion efficiency or quantum efficiency of electron transport) and Rd (daytime dark respiration), were modeled using two third-order polynomial equations and a modified Arrhenius equation. In all species, Vcmax and Jmax increased with soil temperature up to an optimum, and then decreased with further increases in soil temperature. In the conifers, α showed a similar response to soil temperature as Vcmax and Jmax, but soil temperature had no significant effect on α in aspen. Soil temperature had no significant effect on Rd in any species. The three equations described the relationships between soil temperature and the model parameters reasonably well, but performed best for Vcmax and worst for α. No significant relationships were identified between soil temperature and the parameters of the stomatal conductance model. [ABSTRACT FROM PUBLISHER]

Effects of shoot water potential (Ψ) and leaf-to-atmosphere vapor pressure difference (VPD) on gas exchange of jack pine (Pinus banksiana Lamb.), black spruce (Picea mariana (Mill.) B.S.P.), and aspen (Populus tremuloides Michx.) were investigated at the northern edge of the boreal forest in Manitoba, Canada. Laboratory measurements on cut branches showed that net photosynthesis (An) and mesophyll conductance (gm) of jack pine and gm of black spruce did not respond to Ψ until a threshold Ψ was reached below which they decreased linearly. Photosynthesis of black spruce decreased slowly with decreasing Ψ above the threshold and declined more rapidly thereafter. The threshold Ψ was lower in black spruce than in jack pine. However, stomatal conductance (gs) of black spruce decreased continuously with decreasing Ψ, whereas gs of jack pine showed a threshold response. Mesophyll limitations were primarily responsible for the decline in An at low Ψ for jack pine and black spruce in the middle of the growing season, but stomatal limitations became more important later in the season. Field measurements on in situ branches on warm sunny days showed that both conifer species maintained Ψ above the corresponding threshold and there was no evidence of Ψ limitation on An of jack pine, black spruce or aspen.Vapor pressure difference was important in regulating gas exchange in all three species. An empirical model was used to quantify the gs response to VPD. When parameterized with laboratory data for the conifers, the model also fit the corresponding field data. When parameterized with field data, the model showed that stomata of aspen were the most sensitive of the three species to VPD, and stomata of black spruce were the least sensitive. For jack pine and aspen, stomata of foliage in the upper canopy were significantly more sensitive than stomata of foliage in the lower canopy. Vapor pressure difference had a greater impact on An of aspen than on An of the conifers as a result of aspen's greater stomatal sensitivity to VPD and greater slope of the relationship between An and intercellular CO2 concentration (Ci). During the 1994 growing season, VPD averaged 1.0 kPa, corresponding to ratios of Ci to ambient CO2 of 0.77, 0.71 and 0.81 for jack pine, black spruce and aspen, respectively. We conclude that increases in VPD at the leaf surface in response to climate change should affect the absolute CO2 and H2O fluxes per unit leaf area of the aspen component of a boreal forest landscape more than those of the conifer component. [ABSTRACT FROM AUTHOR]

Introduction: Climate change-related CO 2 increases and different forms of nitrogen deposition are thought to affect the performance of plants, but their interactions have been poorly studied., Methods: This study investigated the responses of photosynthesis and growth in two invasive maple species, amur maple ( Acer ginnala Maxim.) and boxelder maple ( Acer negundo L.), to elevated CO 2 (400 µmol mol -1 (aCO 2 ) vs. 800 µmol mol -1 (eCO 2 ) and different forms of nitrogen fertilization (100% nitrate, 100% ammonium, and an equal mix of the two) with pot experiment under controlled conditions., Results and Discussion: The results showed that eCO 2 significantly promoted photosynthesis, biomass, and stomatal conductance in both species. The biochemical limitation of photosynthesis was switched to RuBP regeneration (related to J max ) under eCO 2 from the Rubisco carboxylation limitation (related to V cmax ) under aCO 2 . Both species maximized carbon gain by lower specific leaf area and higher N concentration than control treatment, indicating robust morphological plasticity. Ammonium was not conducive to growth under aCO 2 , but it significantly promoted biomass and photosynthesis under eCO 2 . When nitrate was the sole nitrogen source, eCO 2 significantly reduced N assimilation and growth. The total leaf N per tree was significantly higher in boxelder maple than in amur maple, while the carbon and nitrogen ratio was significantly lower in boxelder maple than in amur maple, suggesting that boxelder maple leaf litter may be more favorable for faster nutrient cycling. The results suggest that increases in ammonium under future elevated CO 2 will enhance the plasticity and adaptation of the two maple species., Competing Interests: The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest. The author(s) declared that they were an editorial board member of Frontiers, at the time of submission. This had no impact on the peer review process and the final decision., (Copyright © 2024 Wang and Dang.)

Elevated CO2 and warmer temperature occur simultaneously under the current climate change. However, their combined effects on the photosynthetic traits in boreal trees are not well understood. This study investigated the morphological and photosynthetic responses of yellow birch (Betula alleghaniensis Britt.) to a combined treatment of CO2 and temperature (ambient, ACT (400 μmol mol-1 CO2 and current temperature) vs elevated, ECT (750 μmol mol-1 CO2 and current +4 °C temperature)). It was found that ECT significantly reduced leaf-area based photosynthetic rate (An), maximum Rubisco carboxylation rate (Vcmax), photosynthetic electron transport rate (Jmax), leaf nitrogen concentration, respiration and mesophyll conductance. There were two interesting findings: first, the primary mechanism of photosynthetic limitation shifted from Ribulose-1,5-bisphosphate (RuBP) carboxylation (related to Vcmax) to RuBP regeneration (related to Jmax) in response to ECT, leading to decreased transition point (Ci-t and An-t) from RuBP carboxylation to regeneration; second, the increase in total leaf area in response to ECT more than compensated for the downregulation of leaf-area based photosynthesis, leading to greater biomass in ECT than in ACT. We proposed a new protocol for evaluating photosynthetic limitations by comparing the relative relationship between the transition point (Ci-t and An-t) and the photosynthetic rate at growth CO2 (Ci-g and An-g). Furthermore, we found that Jmax (RuBP regeneration) was the primary limitation to An under ECT., (© The Author(s) 2022. Published by Oxford University Press. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com.)

The distribution of tree species is expected to shift toward the pole in response to the climate change associated with the elevation of atmospheric CO 2 concentration [CO 2 ]. The shift will expose trees to a new photoperiod regime and other environmental conditions. The changes in these factors will likely have interactive effects on the ecophysiological traits of plants. This study investigated how CO 2 elevation and change in photoperiod influence the timing of bud development, leaf senescence, and cold hardiness in the fall, and bud break in the spring in boreal white birch ( Betula papyrifera Marsh.). Seedlings were exposed to two different [CO 2 ] (AC = 400 μmol mol -1 ; EC = 1000 μmol mol -1 ) and four simulated photoperiod regimes in the greenhouse corresponding to each latitude [48 (seed origin), 52, 55, and 58°N] for two growing seasons. We found that EC advanced the initiation of leaf color change (10% leaf color change) in the fall by 23 days, but delayed the completion date of color change (90%). Leaf senescence started earlier in the photoperiods corresponding to 55 and 58°N latitude than those at 48 and 52°N latitudes under EC, but photoperiod did not affect leaf senescence under AC. Additionally, the temperature causing 50% electrolyte leakage (a measure of susceptibility to freezing damage) was more negative under the photoperiod corresponding to 55° (-46°C) and at 58°N (-60°C) under EC than at the lower latitudes (above -40°C). Budburst in the spring occurred earlier under the photoperiods corresponding to the two highest latitudes under EC, but the trend was opposite under AC. The combination of longer photoperiods and elevated [CO 2 ] resulted in earlier budburst in the spring and later completion of leaf senescence in the fall as well as greater cold hardiness, leading to extended growing seasons from both ends. However, the onset of leaf senescence was earlier than in other treatment combinations. Furthermore, the photoperiod effects were quite different under the ambient [CO 2 ]. Our results suggest that it is extremely important to consider the complex interactions of [CO 2 ] and photoperiod in planning latitudinal seed transfers and in predicting the migration of boreal trees in response to climate change., (Copyright © 2020 Tedla, Dang and Inoue.)

White birch (Betula paperifera Mash) seedlings were exposed to progressively warming in greenhouses under ambient and elevated CO 2 concentrations for 5 months to explore boreal tree species' potential capacity to acclimate to global climate warming and CO 2 elevation. In situ foliar gas exchange, in vivo carboxylation characteristics and chlorophyll fluorescence were measured at temperatures of 26 (o)C and 37 (o)C. Elevated CO 2 significantly increased net photosynthetic rate (Pn) at both measurement temperatures, and Pn at 37 (o)C was higher than that at 26 (o)C under elevated CO 2. Stomatal conductance (gs) was lower at 37 (o)C than at 26 (o)C, while transpiration rate (E) was higher at 37 (o)C than that at 26 (o)C. Elevated CO 2 significantly increased instantaneous water-use efficiency (WUE) at both 26 (o)C and 37 (o)C, but WUE was markedly enhanced at 37 (o)C under elevated CO 2. The effect of temperature on maximal carboxylation rate (Vcmax), PAR-saturated electron transport rate (Jmax) and triose phosphate utilization (TPU) varied with CO 2, and the Vcmax and Jmax were significantly higher at 37 (o)C than at 26 (o)C under elevated CO 2. However, there were no significant interactive effects of CO 2 and temperature on TPU. The actual photochemical efficiency of PSII (DF/ Fm'), total photosynthetic linear electron transport rate through PSII (JT) and the partitioning of JT to carboxylation (Jc) were higher at 37 (o)C than at 26 (o)C under elevated CO 2. Elevated CO 2 significantly suppressed the partitioning of JT to oxygenation (Jo/JT). The data suggest that the CO 2 elevation and progressive warming greatly enhanced photosynthesis in white birch seedlings in an interactive fashion.

To study the effects of elevated CO2 concentration ([CO2]) on relationships between nitrogen (N) nutrition and foliar gas exchange parameters, white birch (Betula papyrifera Marsh.) seedlings were exposed to one of five N-supply regimes (10, 80, 150, 220, 290 mg N l(-1)) in either ambient [CO2] (360 micromol mol(-1)) or elevated [CO2] (720 micromol mol(-1)) in environment-controlled greenhouses. Foliar gas exchange and chlorophyll fluorescence were measured after 60 and 80 days of treatment. Photosynthesis showed a substantial down-regulation (up to 57%) in response to elevated [CO2] and the magnitude of the down-regulation generally decreased exponentially with increasing leaf N concentration. When measured at the growth [CO2], elevated [CO2] increased the overall rate of photosynthesis (P(n)) and instantaneous water-use efficiency (IWUE) by up to 69 and 236%, respectively, but decreased transpiration (E) and stomatal conductance (g(s)) in all N treatments. However, the degree of stimulation of photosynthesis by elevated [CO2] decreased as photosynthetic down-regulation increased from 60 days to 80 days of treatment. Elevated [CO2] significantly increased total photosynthetic electron transport in all N treatments at 60 days of treatment, but the effect was insignificant after 80 days of treatment. Both P(n) and IWUE generally increased with increasing leaf N concentration except at very high leaf N concentrations, where both P(n) and IWUE declined. The relationships of P(n) and IWUE with leaf N concentration were modeled with both a linear regression and a second-order polynomial function. Elevated [CO2] significantly and substantially increased the slope of the linear regression for IWUE, but had no significant effect on the slope for P(n). The optimal leaf N concentration for P(n) and IWUE derived from the polynomial function did not differ between the CO2 treatments when leaf N was expressed on a leaf area basis. However, the mass-based optimal leaf N concentration for P(n) was much lower in seedlings in elevated [CO2] than in ambient [CO2] (31.88 versus 37.00 mg g(-1)). Elevated [CO2] generally decreased mass-based leaf N concentration but had no significant effect on area-based leaf N concentration; however, maximum N concentration per unit leaf area was greater in elevated [CO2] than in ambient [CO2] (1.913 versus 1.547 g N m(-2)).

A coupled photosynthesis-stomatal conductance model was parameterized and tested with branches of black spruce (Picea mariana (Mill.) B.S.P.) and jack pine (Pinus banksiana Lamb.) trees growing in the Northern Study Area of the Boreal Ecosystem-Atmosphere Study (BOREAS) in Manitoba, Canada. Branch samples containing foliage of all age-classes were harvested from a lowland old black spruce (OBS) and an old jack pine (OJP) stand and the responses of photosynthesis (A(n)) and stomatal conductance (g(s)) to temperature, CO(2), light, and leaf-to-air vapor pressure difference (VPD) were determined under controlled laboratory conditions at the beginning, middle, and end of the growing season (Intensive Field Campaigns (IFC) 1, 2, and 3, respectively). The parameterized model was then tested against in situ field gas-exchange measurements in a young jack pine (YJP) and an upland black spruce (UBS) stand as well as in the OBS and OJP stands. Parameterization showed that Rubisco capacity (V(max)), apparent quantum yield (alpha') and Q(10) for sink limitation were the most crucial parameters for the photosynthesis sub-model and that V(max) varied among different measurement series in the laboratory. Verification of the model against the data used to parameterize it yielded correlation coefficients (r) of 0.97 and 0.93 for black spruce and jack pine, respectively, when IFC-specific parameters were used, and 0.77 and 0.87 when IFC-2 parameters were applied to all IFCs. For both measured and modeled g(s), the stomatal conductance sub-model, which linearly relates g(s) to (A(n)h(s))/c(s) (where h(s) and c(s) are relative humidity and CO(2) mole fraction at the leaf surface, respectively), had significantly steeper slopes and higher r values when only the VPD response data were used for parameterization than when all of the response data were used for parameterization. Testing the photosynthesis sub-model against upper canopy field data yielded poor results when laboratory estimates of V(max) were used. Use of the mean V(max) estimated for all upper canopy branches measured on a given day improved model performance for jack pine (from a nonsignificant correlation between measured and modeled A(n) to r = 0.45), but not for black spruce (r = 0.45 for both cases). However, when V(max) was estimated for each branch sample individually, the model accurately predicted the 23 to 137% diurnal variation in A(n) for all stands for both the upper and lower canopy. This was true both when all of the other parameters were IFC-specific (r = 0.93 and 0.92 for black spruce and jack pine, respectively) and when only mid-growing season (IFC-2) values were used (r = 0.92 for both species). Branch-specific V(max) estimates also permitted accurate prediction of field g(s) (r = 0.75 and 0.89 for black spruce and jack pine, respectively), although parameterization with all of the response data overestimated g(s) in the field, whereas parameterization with only the VPD response data provided unbiased predictions. Thus, after parameterization with the laboratory data, accurately modeling the range of A(n) and g(s) encountered in the field for both black spruce and jack pine was reduced to a single unknown parameter, V(max).