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Drought invokes a variety of metabolic alterations in plant leaves to cope with stress situations. To understand the effects of CO2 and drought stress for leaf metabolic changes in potato [Solanum tuberosum (L)], two contrasting potato cultivars Harley Blackwell (HB, an early maturing, newer cultivar) and Snowden (SD, an established, full-season cultivar) were tested under water-limited conditions and CO2 enrichment. The results revealed that most of the drought-triggered metabolites were lower in HB compared to SD. However, HB showed quicker adjustments in the metabolic processes such as conversion of starch into soluble sugars and biosynthesis of phenylalanine and other compatible solutes at the early stages of the drought progression. Moreover, the existence of genotypic differences for leaf water potential (LWP) in response to CO2 enrichment was evident. Our study provides insights into the possible metabolic strategies of drought tolerance in potato cultivars under ambient and elevated CO2. [ABSTRACT FROM AUTHOR]

Detached leaves at top canopy structures always experience higher solar irradiance and leaf temperature under natural conditions. The ability of tolerance to high temperature represents thermotolerance potential of whole-plants, but was less of concern. In this study, we used a heat-tolerant (B76) and a heat-susceptible (B106) maize inbred line to assess the possible mitigation of sudden heat shock (SHS) effects on photosynthesis (PN) and C4 assimilation pathway by elevated [CO2]. Two maize lines were grown in field-based open top chambers (OTCs) at ambient and elevated (+180 ppm) [CO2]. Top-expanded leaves for 30 days after emergence were suddenly exposed to a 45°C SHS for 2 hours in midday during measurements. Analysis on thermostability of cellular membrane showed there was 20% greater electrolyte leakage in response to the SHS in B106 compared to B76, in agreement with prior studies. Elevated [CO2] protected PN from SHS in B76 but not B106. The responses of PN to SHS among the two lines and grown CO2 treatments were closely correlated with measured decreases of NADP-ME enzyme activity and also to its reduced transcript abundance. The SHS treatments induced starch depletion, the accumulation of hexoses and also disrupted the TCA cycle as well as the C4 assimilation pathway in the both lines. Elevated [CO2] reversed SHS effects on citrate and related TCA cycle metabolites in B106 but the effects of elevated [CO2] were small in B76. These findings suggested that heat stress tolerance is a complex trait, and it is difficult to identify biochemical, physiological or molecular markers that accurately and consistently predict heat stress tolerance. [ABSTRACT FROM AUTHOR]

A detailed investigation of the concentration (e.g., mg g-1 seed) and total yield (e.g., g plant-1) of seed mineral elements and metabolic profile under phosphorus (P) starvation at ambient (aCO2) and elevated carbon dioxide (eCO2) in soybean is limited. Soybean plants were grown in a controlled environment at either sufficient (0.50 mM P, control) or deficient (0.10 and 0.01 mM, P-stress) levels of P under aCO2 and eCO2 (400 and 800 mmol mol-1, respectively). Both the concentration and yield of 36 out of 38 seed components responded to P treatment and on average 25 and 11 components increased and decreased, respectively, in response to P starvation. Concentrations of carbohydrates (e.g., glucose, sugar alcohols), organic acids (e.g., succinate, glycerate) and amino acids increased while oil, and several minerals declined under P deficiency. However, the yield of the majority of seed components declined except several amino acids (e.g., phenylalanine, serine) under P deficiency. The concentration-based relationship between seed protein and oil was negative (r² = 0.96), whereas yield-based relationship was positive (r² = 0.99) across treatments. The CO2 treatment also altered the concentration of 28 out of 38 seed components, of which 23 showed decreasing (e.g., sucrose, glucose, citrate, aconitate, several minerals, and amino acids) while C, iron, Mn, glycerate, and oil showed increasing trends at eCO2. Despite a decreased concentration, yields of the majority of seed components were increased in response to eCO2, which was attributable to the increased seed production especially near sufficient P nutrition. The P × CO2 interactions for the concentration of amino acids and the yield of several components were due to the lack of their response to eCO2 under control or the severe P starvation, respectively. Thus, P deficiency primarily reduced the concentration of oil and mineral elements but enhanced a majority of other components. However, seed components yield consistently declined under P starvation except for several amino acids. The study highlighted a P nutritional-status dependent response of soybean seed components to eCO2 suggesting the requirement of an adequate P supply to obtain the beneficial effects of eCO2 on the overall yield of various seed components. [ABSTRACT FROM AUTHOR]

To evaluate the combined effect of temperature and CO 2 on photosynthetic processes, leaf metabolites and growth, soybean was grown under a controlled environment at low (22/18 °C, LT), optimum (28/24 °C, OT) and high (36/32 °C HT) temperatures under ambient (400 μmol mol −1 ; aCO 2 ) or elevated (800 μmol mol −1 ; eCO 2 ) CO 2 concentrations during the reproductive stage. In general, the rate of photosynthesis ( A ), stomatal ( g s ) and mesophyll ( g m ) conductance, quantum yield of photosystem II, rates of maximum carboxylation ( V Cmax ), and electron transport ( J ) increased with temperature across CO 2 levels. However, compared with OT, the percentage increases in these parameters at HT were lower than the observed decline at LT. The photosynthetic limitation at LT and OT was primarily caused by photo-biochemical processes (49–58%, L b ) followed by stomatal (27–32%, L s ) and mesophyll (15–19%, L m ) limitations. However, at HT, it was primarily caused by L s (41%) followed by L b (33%) and L m (26%). The dominance of L b at LT and OT was associated with the accumulation of non-structural carbohydrates (e.g., starch) and several organic acids, whereas this accumulation did not occur at HT, indicating increased metabolic activities. Compared with OT, biomass and seed yield declined more at HT than at LT. The eCO 2 treatment compensated for the temperature-stress effects on biomass but only partially compensated for the effects on seed yield, especially at HT. Photosynthetic downregulation at eCO 2 was possibly due to the accumulation of non-structural carbohydrates and the decrease in g s and A std (standard A measured at 400 μmol mol −1 sub-stomatal CO 2 concentration), as well as the lack of CO 2 effect on g m , V Cmax , and J , and photosynthetic limitation. Thus, the photosynthetic limitation was temperature-dependent and was primarily influenced by the alteration in photo-biochemical processes and metabolic activities. Despite the inconsistent response of photosynthesis (or biomass accumulation) and seed yield, eCO 2 tended to fully or partially compensate for the adverse effect of the respective LT and HT stresses under well-watered and sufficient nutrient conditions. [ABSTRACT FROM AUTHOR]

Changes in the stomatal aperture in response to CO 2 levels allow plants to manage water usage, optimize CO 2 uptake and adjust to environmental stimuli. The current study reports that sub-ambient CO 2 up-regulated the low temperature induction of the C-repeat Binding Factor (CBF)-dependent cold signaling pathway in Arabidopsis ( Arabidopsis thaliana ) and the opposite occurred in response to supra-ambient CO 2 . Accordingly, cold induction of various downstream cold-responsive genes was modified by CO 2 treatments and expression changes were either partially or fully CBF-dependent. Changes in electrolyte leakage during freezing tests were correlated with CO 2' s effects on CBF expression. Cold treatments were also performed on Arabidopsis mutants with altered stomatal responses to CO 2 , i.e., high leaf temperature 1-2 ( ht1-2 , CO 2 hypersensitive) and β-carbonic anhydrase 1 and 4 ( ca1ca4 , CO 2 insensitive). The cold-induced expression of CBF and downstream CBF target genes plus freezing tolerance of ht1-2 was consistently less than that for Col-0, suggesting that HT1 is a positive modulator of cold signaling. The ca1ca4 mutant had diminished CBF expression during cold treatment but the downstream expression of cold-responsive genes was either similar to or greater than that of Col-0. This finding suggested that βCA1/4 modulates the expression of certain cold-responsive genes in a CBF-independent manner. Stomatal conductance measurements demonstrated that low temperatures overrode low CO 2 -induced stomatal opening and this process was delayed in the cold tolerant mutant, ca1ca4 , compared to the cold sensitive mutant, ht1-2 . The similar stomatal responses were evident from freezing tolerant line, Ox-CBF, overexpression of CBF3, compared to wild-type ecotype Ws-2. Together, these results indicate that CO 2 signaling in stomata and CBF-mediated cold signaling work coordinately in Arabidopsis to manage abiotic stress.

A detailed investigation of the concentration (e.g., mg g -1 seed) and total yield (e.g., g plant -1 ) of seed mineral elements and metabolic profile under phosphorus (P) starvation at ambient (aCO 2 ) and elevated carbon dioxide (eCO 2 ) in soybean is limited. Soybean plants were grown in a controlled environment at either sufficient (0.50 mM P, control) or deficient (0.10 and 0.01 mM, P-stress) levels of P under aCO 2 and eCO 2 (400 and 800 μmol mol -1 , respectively). Both the concentration and yield of 36 out of 38 seed components responded to P treatment and on average 25 and 11 components increased and decreased, respectively, in response to P starvation. Concentrations of carbohydrates (e.g., glucose, sugar alcohols), organic acids (e.g., succinate, glycerate) and amino acids increased while oil, and several minerals declined under P deficiency. However, the yield of the majority of seed components declined except several amino acids (e.g., phenylalanine, serine) under P deficiency. The concentration-based relationship between seed protein and oil was negative ( r 2 = 0.96), whereas yield-based relationship was positive ( r treatment also altered the concentration of 28 out of 38 seed components, of which 23 showed decreasing (e.g., sucrose, glucose, citrate, aconitate, several minerals, and amino acids) while C, iron, Mn, glycerate, and oil showed increasing trends at eCO 2 = 0.99) across treatments. The CO 2 treatment also altered the concentration of 28 out of 38 seed components, of which 23 showed decreasing (e.g., sucrose, glucose, citrate, aconitate, several minerals, and amino acids) while C, iron, Mn, glycerate, and oil showed increasing trends at eCO 2 . Despite a decreased concentration, yields of the majority of seed components were increased in response to eCO 2 , which was attributable to the increased seed production especially near sufficient P nutrition. The P × CO 2 interactions for the concentration of amino acids and the yield of several components were due to the lack of their response to eCO 2 under control or the severe P starvation, respectively. Thus, P deficiency primarily reduced the concentration of oil and mineral elements but enhanced a majority of other components. However, seed components yield consistently declined under P starvation except for several amino acids. The study highlighted a P nutritional-status dependent response of soybean seed components to eCO 2 suggesting the requirement of an adequate P supply to obtain the beneficial effects of eCO 2 on the overall yield of various seed components.

Elevated growth temperatures are known to affect foliar organic acid concentrations in various plant species. In the current study, citrate, malate, malonate, fumarate and succinate decreased 40 to 80% in soybean leaflets when plants were grown continuously in controlled environment chambers at 36/28 compared to 28/20 °C. Temperature effects on the above mentioned organic acids were partially reversed three days after plants were transferred among optimal and supra-optimal growth temperatures. In addition, CO2 enrichment increased foliar malate, malonate and fumarate concentrations in the supra-optimal temperature treatment, thereby mitigating effects of high temperature on respiratory metabolism. Glycerate, which functions in the photorespiratory pathway, decreased in response to CO2 enrichment at both growth temperatures. The above findings suggested that diminished levels of organic acids in soybean leaflets upon exposure to high growth temperatures were attributable to metabolic impairment and to changes of photorespiratory flux. Leaf development rates differed among temperature and CO2 treatments, which affected foliar organic acid levels. Additionally, we report that large decreases of foliar organic acids in response to elevated growth temperatures were observed in legume species.