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The function of landscape plants on the ecosystem can alleviate environmental issues of urbanization and global change. Global changes due to elevated CO 2 affect plant growth and survival, but there is a lack of quantitative methods to evaluate the adaptability of landscape plants to future climate conditions. Leaf traits characterized by leaf economic spectrum (LES) are the universal currency for predicting the impact on plant ecosystem functions. Elevated CO 2 usually leads to photosynthetic acclimation (PC), characterised by decreased photosynthetic capacity. Here, we proposed a theoretical and practical framework for the use of LES and PC to project the potential performance of landscape plants under future climatic conditions through principal component analysis, structural equation modelling, photosynthetic restriction analysis and nitrogen allocation analysis. We used wintersweet (an important landscaping species) to test the feasibility of this framework under elevated CO 2 and different nitrogen (N) supplies. We found that elevated CO 2 decreased the specific leaf area but increased leaf N concentration. The results suggest wintersweet may be characterized by an LES with high leaf construction costs, low photosynthetic return, and robust stress resistance. Elevated CO 2 reduced photosynthetic capacity and stomatal conductance but increased photosynthetic rate and leaf area. These positive physio-ecological traits, e.g., larger leaf area (canopy), higher water use efficiency and stress resistance, may lead to improved performance of wintersweet under the predicted future climatic conditions. The results suggest planting more wintersweet in urban landscaping may be an effective adaptive strategy to climate change., (© 2024 Scandinavian Plant Physiology Society.)

To investigate the interactive effects of soil temperature (T(soil)) and nutrient availability on the response of photosynthesis to elevated atmospheric carbon dioxide concentration ([CO(2)]), white birch (Betula papyrifera Marsh.) seedlings were exposed to ambient (360 micromol mol(-1)) or elevated (720 micromol mol(-1)) [CO(2)], three T(soil) (5, 15 and 25 degrees C initially, increased to 7, 17 and 27 degrees C, respectively, 1 month later) and three nutrient regimes (4/1.8/3.3, 80/35/66 and 160/70/132 mg l(-1) N/P/K) for 3 months in environment-controlled greenhouses. Elevated [CO(2)] increased net photosynthetic rate (A(n)), instantaneous water-use efficiency (IWUE), internal to ambient carbon dioxide concentration ratio (C(i)/C(a)), triose phosphate utilization (TPU) and photosynthetic linear electron transport to carboxylation (J(c)), and it decreased actual photochemical efficiency of photosystem II (DeltaF/F(m)'), the fraction of total linear electron transport partitioned to oxygenation (J(o)/J(T)) and leaf N concentration. The low T(soil) suppressed A(n), transpiration rate (E), TPU, DeltaF/F(m)' and J(c), but it increased J(o)/J(T). The low nutrient treatment reduced A(n), IWUE, maximum carboxylation rate of Rubisco, light-saturated electron transport rate, TPU, DeltaF/F(m)', J(c) and leaf N concentration, but increased C(i)/C(a). There were two-factor interactions for C(i)/C(a), TPU and leaf N concentration, and a significant effect of CO(2) x T(soil) x nutrient regime on A(n), IWUE and J(c). The stimulations of A(n) and IWUE by elevated [CO(2)] were limited to seedlings grown under the intermediate and high nutrient regimes at the intermediate and high T(soil). For J(c), the [CO(2)] effect was significant only at intermediate T(soil) + high nutrient availability. No significant [CO(2)] effects were observed under the low T(soil) at any nutrient level. Our results support this study's hypothesis that low T(soil) would reduce the positive effect of high nutrient supply on the response of A(n) to elevated [CO(2)].

White birch (Betula papyrifera Marsh.) seedlings were grown under two carbon dioxide concentrations (ambient: 360 micromol mol(-1) and elevated: 720 micromol mol(-1)), three soil temperatures (5, 15 and 25 degrees C initially, increased to 7, 17 and 27 degrees C, respectively, 1 month later) and three moisture regimes (low: 30-40%; intermediate: 45-55% and high: 60-70% field water capacity) in greenhouses. In situ gas exchange and chlorophyll fluorescence were measured after 2 months of treatments. Net photosynthetic rate (A(n)) of seedlings grown under the intermediate and high moisture regimes increased from low to intermediate T(soil) and then decreased to high T(soil). There were no significant differences between the low and high T(soil), with the exception that A(n) was significantly higher under high than low T(soil) at the high moisture regime. No significant T(soil) effect on A(n) was observed at the low moisture regime. The intermediate T(soil) increased stomatal conductance (g(s)) only at intermediate and high but not at low moisture regime, whereas there were no significant differences between the low and high T(soil) treatments. Furthermore, the difference in g(s) between the intermediate and high T(soil) at high moisture regime was not statistically significant. The low moisture regime significantly reduced the internal to ambient CO2 concentration ratio at all T(soil). There were no significant individual or interactive effects of treatment on maximum carboxylation rate of Rubisco, light-saturated electron transport rate, triose phosphate utilization or potential photochemical efficiency of photosystem II. The results of this study suggest that soil moisture condition should be taken into account when predicting the responses of white birch to soil warming.

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)).

To investigate the interactive effects of atmospheric carbon dioxide concentration ([CO(2)]) and nutrition on photosynthesis and its acclimation to elevated [CO(2)], a two-way factorial experiment was carried out with two nutritional regimes (high- and low-nitrogen (N), phosphorus (P) and potassium (K)) and two CO(2) concentrations (360 and 720 ppm) with white birch seedlings (Betula papyrifera Marsh.) grown for four months in environment-controlled greenhouses. Elevated [CO(2)] enhanced maximal carboxylation rate (V(cmax)), photosynthetically active radiation-saturated electron transport rate (J(max)), actual photochemical efficiency of photosystem II (PSII) in the light (DeltaF/F(m)') and photosynthetic linear electron transport to carboxylation (J(c)) after 2.5 months of treatment, and it increased net photosynthetic rate (A(n)), 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 (g(s)), transpiration rate (E) and the fraction of total photosynthetic linear electron transport partitioned to oxygenation (J(o)/J(T)) after 2.5 and 3.5 months of treatment. Low nutrient availability decreased A(n), WUE, V(cmax), J(max), triose phosphate utilization (TPU), (/F(m)' - F)//F(m)' and J(c), but increased J(o)/J(T) and NUE. Generally, V(cmax) was more sensitive to nutrient availability than J(max). There were significant interactive effects of [CO(2)] and nutrition over time, e.g., the positive effects of high nutrition on A(n), V(cmax), J(max), DeltaF/F(m)' and J(c) were significantly greater in elevated [CO(2)] than in ambient [CO(2)]. In contrast, the interactive effect of [CO(2)] 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 [CO(2)], 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 [CO(2)] 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.

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 degrees C initially, increased to 10, 20 and 30 degrees 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 (g(s)) and transpiration rate (E) in jack pine in both CO2 treatments and g(s) 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 g(s) 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 (DeltaF/Fm') in jack pine, but decreased DeltaF/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/J(T)) 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/J(T) in both species at both measurement times except Jc in white birch after 2.5 months of treatment. Elevated [CO2] also decreased g(s) 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 DeltaF/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].

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 degrees C for 4 months. Light and CO(2) response curves of foliar gas exchange were measured for model parameterization. The effects of soil temperature on four key model parameters, V(cmax) (maximum rate of carboxylation), J(max) (maximum rate of electron transport), alpha (energy conversion efficiency or quantum efficiency of electron transport) and R(d) (daytime dark respiration), were modeled using two third-order polynomial equations and a modified Arrhenius equation. In all species, V(cmax) and J(max) increased with soil temperature up to an optimum, and then decreased with further increases in soil temperature. In the conifers, alpha showed a similar response to soil temperature as V(cmax) and J(max), but soil temperature had no significant effect on alpha in aspen. Soil temperature had no significant effect on R(d) in any species. The three equations described the relationships between soil temperature and the model parameters reasonably well, but performed best for V(cmax) and worst for alpha. No significant relationships were identified between soil temperature and the parameters of the stomatal conductance model.

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]

In response to global warming, trees are expected to shift their distribution ranges to higher latitudes. The range shift will expose them to novel environmental conditions, such as new photoperiod regimes. These factors can interact with rising atmospheric CO2 ([CO2]) to affect trees' physiology and growth. This study simulated future environmental conditions to investigate photosynthetic responses to changes in photoperiod regimes (seed origin [48°N], 52, 55, and 58°N) and [CO2] (ambient 400 vs. elevated 1000 μmol mol−1) in white birch (Betula papyrifera Marsh.) seedlings. Our results show that elevated [CO2] stimulated leaf photosynthesis (Pn) at the two lower latitudes (48 and 52°N). However, this stimulation by elevated [CO2] was lost in the two higher latitudes (55 and 58°N). Elevated [CO2] led to the downregulation of maximum Rubisco activity (Vcmax) for the two higher latitudes, and maximum electron transport rate (Jmax) and triose phosphate utilization (TPU) at 58°N, while it enhanced Jmax and TPU for the two lower latitudes. Increased instantaneous water‐use efficiency (IWUE) for the two lower latitudes was primarily attributed to the CO2 stimulation of Pn while the higher IWUE under the photoperiod regimes of 55 and 58°N latitudes was explained by reduced water loss. Photoperiod effects varied with [CO2]: Pn increased at the photoperiod regimes of 55 and 58°N in ambient [CO2] while it tended to decline under these photoperiods in elevated [CO2]. Our study suggests that the photosynthesis of white birch will likely respond negatively to northward migration or seed transfer in response to climate change. [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]

Predicting the future distribution of plants requires a mechanistic understanding of how plants cope with their new environmental conditions under a changed climate. We examined the effects of elevated carbon concentration ([CO2]) and elevated Tsoil on the physiological responses to light of a shade-tolerant woody species, mountain maple (Acer spicatum L.). Seedlings were exposed to ambient and elevated [CO2] (392μmolmol−1 vs. 784μmolmol−1), current and elevated soil temperatures (Tsoil 17 vs. 22°C) at high and low (100% vs. 30%) light conditions for one growing season. It was found that elevated Tsoil stimulated net photosynthesis (A) by 18% in the low-light treatment but tended to reduce A in the high-light treatment. Elevated [CO2] increased A by 100% under the elevated Tsoil and by 48% at the current Tsoil. The effect of elevated Tsoil also varied with [CO2]: it increased A by 13% under the elevated [CO2] but reduced A by 17% under the ambient [CO2]. We observed a significant increase in the instantaneous water-use efficiency of photosynthesis (IWUE) in response to the high-light treatment under the elevated [CO2] but not under the ambient [CO2]. Our data indicate that the elevated [CO2] markedly increased nitrogen (N) allocation to the photochemical apparatus of A in seedlings grown under the high-light condition. These results suggest that the predicted increases in atmospheric [CO2] will likely enhance the growth of mountain maple in canopy gaps in the forest, while the predicted elevated Tsoil will negate the benefit of high-light conditions. [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]

Abstract: To study the effects of source–sink ratio and nutrient supply on photosynthetic acclimation to CO2 elevation, we subjected white birch seedlings to two levels of nutrient supply (high vs. low) and CO2 concentrations (ambient vs. doubled [CO2]) for two months and then shaded the lower canopy on half of the seedlings to reduce source/sink ratio for an additional month. The CO2 elevation significantly increased P n and IWUE at both nutrient levels but the increase was greater in the high than low nutrient treatment. The CO2 elevation resulted in a down-regulation of V cmax in the low nutrient treatment but up-regulation of J max, TPU, and J c in the high nutrient after 3 months of treatment. Both the CO2 elevation and high nutrient supply increased the partition of total electron transport to carboxylation at the expense of oxidation. The seedlings responded to the shading of the lower canopy by reducing biomass allocation to roots rather than making physiological adjustments to unshaded leaves in the upper canopy. Our results suggest that the direction of photosynthetic acclimation to CO2 elevation in white birch was nutrient-dependent and an increase in sink strength could reduce the feedback inhibition of photosynthesis. [Copyright &y& Elsevier]

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]