Acclimation of peanut (Arachis hypogaea L.) leaf photosynthesis to elevated growth CO2 and temperature

Peanut (Arachis hypogaea L. cv. Florunner) was grown from seed sowing to plant maturity under two daytime CO₂ concentrations ([CO₂]) of 360 μmol mol⁻¹ (ambient) and 720 μmol mol⁻¹ (elevated) and at two temperatures of 1.5 and 6.0 °C above ambient temperature. The objectives were to characterize peanut leaf photosynthesis responses to long-term elevated growth [CO₂] and temperature, and to assess whether elevated [CO₂] regulated peanut leaf photosynthetic capacity, in terms of activity and protein content of ribulose bisphosphate carboxylase-oxygenase (Rubisco), Rubisco photosynthetic efficiency, and carbohydrate metabolism. At both growth temperatures, leaves of plants grown under elevated [CO₂] had higher midday photosynthetic CO₂ exchange rate (CER), lower transpiration and stomatal conductance and higher water-use efficiency, compared to those of plants grown at ambient [CO₂]. Both activity and protein content of Rubisco, expressed on a leaf area basis, were reduced at elevated growth [CO₂]. Declines in Rubisco under elevated growth [CO₂] were 27–30% for initial activity, 5–12% for total activity, and 9–20% for protein content. Although Rubisco protein content and activity were down-regulated by elevated [CO₂], Rubisco photosynthetic efficiency, the ratio of midday light-saturated CER to Rubisco initial or total activity, of the elevated-[CO₂] plants was 1.3- to 1.9-fold greater than that of the ambient-[CO₂] plants at both growth temperatures. Leaf soluble sugars and starch of plants grown at elevated [CO₂] were 1.3- and 2-fold higher, respectively, than those of plants grown at ambient [CO₂]. Under elevated [CO₂], leaf soluble sugars and starch, however, were not affected by high growth temperature. In contrast, high temperature reduced leaf soluble sugars and starch of the ambient-[CO₂] plants. Activity of sucrose-P synthase, but not adenosine 5′-diphosphoglucose pyrophosphorylase, was up-regulated under elevated growth [CO₂]. Thus, in the absence of other environmental stresses, peanut leaf photosynthesis would perform well under rising atmospheric [CO₂] and temperature as predicted for this century.     

Effect of elevated temperature and water availability on CO2 exchange and nitrogen fixation of nodulated alfalfa plants

The aim of this study was to investigate the effects of predicted temperature increases and drought conditions of Mediterranean environments on N₂-fixing alfalfa plants. One-month-old plants inoculated with Sinorhizobium meliloti strain 102F78 were grown in growth chambers under different temperature (25/15 or 28/18 °C, day/night) and water availability (control or drought) regimes. Elevated temperature and drought reduced plant dry mass and leaf area, especially when both stresses were combined. The inhibitory effect of elevated temperature on plant growth was a consequence of decreased CO₂ and N₂ fixation rates. A photosynthetic decrease resulted from the inhibition of rubisco activity, probably associated with a lower activation state. An absence of differences in photosynthesis in relation to water availability suggests that drought decreased plant growth due to its negative effect on leaf area. Rising temperature and drought affected the nitrogen content negatively, although effects differed. Elevated temperature inhibited nodule activity drastically, whereas the inhibitory effect resulting from drought centred on nodule dry mass (DM) production. Plants exposed to a combination of elevated temperature and drought were the most negatively affected.     

Elevated CO2 and water-availability effect on gas exchange and nodule development in N2-fixing alfalfa plants

N₂-fixing alfalfa plants were grown in controlled conditions at different CO₂ levels (350 μmol mol^?1 versus 700 μmol mol^?1) and water-availability conditions (WW, watered at maximum pot water capacity versus WD, watered at 50% of control treatments) in order to determine the CO₂ effect (and applied at two water regimes) on plant growth and nodule activity in alfalfa plants. The CO₂ stimulatory effect (26% enhancement) on plant growth was limited to WW plants, whereas no CO₂ effect was observed in WD plants. Exposure to elevated CO₂ decreased Rubisco carboxylation capacity of plants, caused by a specific reduction in Rubisco (EC 4.1.1.39) concentration (11% in WW and 43% in WD) probably explained by an increase in the leaf carbohydrate levels. Plants grown at 700 μmol mol^?1 CO₂ maintained control photosynthetic rates (at growth conditions) by diminishing Rubisco content and by increasing nitrogen use efficiency. Interestingly, our data also suggest that reduction in shoot N demand (reflected by the TSP and especially Rubisco depletion) affected negatively nodule activity (malate dehydrogenase, EC 1.1.1.37, and glutamate-oxaloacetate transaminase, EC 2.6.1.1, activities) particularly in water-limited conditions. Furthermore, nodule DM and TSS data revealed that those nodules were not capable to overcome C sink strength limitations.     

The mechanism(s) involved in the photoprotection of PSII at elevated CO2 in nodulated alfalfa plants

In a previous study, we found that enhanced CO₂ subjected to nodulated alfalfa plants grown at different temperatures (ambient and ambient + 4 °C) and water availability regimes could protect PSII from photodamage. The main objective of this study was to determine the mechanism(s) involved in the photoprotection of PSII at elevated CO₂ levels in this plant. Elevated CO₂ reduced carboxylation capacity-induced photosynthetic acclimation and reduced enzymatic and/or nonenzymatic antioxidant activities, suggesting that changes in electron flow did not cause any photooxidative damage (which was also confirmed by H₂O₂ and lipid peroxidation analyses). Enhanced nonphotochemical quenching and xanthophyll cycle pigments revealed that plants grown at 700 μmol mol⁻¹ CO₂ compensated for the reduction in energy sink with a larger capacity for nonphotochemical dissipation of excitation energy as heat, i.e., modulating the status of the VAZ components. Elevated CO₂ induced the de-epoxidation of violaxanthin to zeaxanthin, facilitating thermal dissipation and protecting the photosynthetic apparatus against the deleterious effect of excess excitation energy.     

The mechanism(s) involved in the photoprotection of PSII at elevated CO2 in nodulated alfalfa plants

In a previous study, we found that enhanced CO₂ subjected to nodulated alfalfa plants grown at different temperatures (ambient and ambient + 4 °C) and water availability regimes could protect PSII from photodamage. The main objective of this study was to determine the mechanism(s) involved in the photoprotection of PSII at elevated CO₂ levels in this plant. Elevated CO₂ reduced carboxylation capacity-induced photosynthetic acclimation and reduced enzymatic and/or nonenzymatic antioxidant activities, suggesting that changes in electron flow did not cause any photooxidative damage (which was also confirmed by H₂O₂ and lipid peroxidation analyses). Enhanced nonphotochemical quenching and xanthophyll cycle pigments revealed that plants grown at 700 μmol mol^?1 CO₂ compensated for the reduction in energy sink with a larger capacity for nonphotochemical dissipation of excitation energy as heat, i.e., modulating the status of the VAZ components. Elevated CO₂ induced the de-epoxidation of violaxanthin to zeaxanthin, facilitating thermal dissipation and protecting the photosynthetic apparatus against the deleterious effect of excess excitation energy.     

Gas exchange acclimation to elevated CO2 in upper-sunlit and lower-shaded canopy leaves in relation to nitrogen acquisition and partitioning in wheat grown in field chambers

Growth at elevated CO₂ often decreases photosynthetic capacity (acclimation) and leaf N concentrations. Lower-shaded canopy leaves may undergo both CO₂ and shade acclimation. The relationship of acclimatory responses of flag and lower-shaded canopy leaves of wheat (Triticum aestivum L.) to the N content, and possible factors affecting N gain and distribution within the plant were investigated in a wheat crop growing in field chambers set at ambient (360 μmol mol⁻¹) and elevated (700 μmol mol⁻¹) CO₂, and with two amounts of N fertilizer (none and 70 kg ha⁻¹ applied on 30 April). Photosynthesis, stomatal conductance and transpiration at a common measurement CO₂, chlorophyll and Rubisco levels of upper-sunlit (flag) and lower-shaded canopy leaves were significantly lower in elevated relative to ambient CO₂-grown plants. Both whole shoot N and leaf N per unit area decreased at elevated CO₂, and leaf N declined with canopy position. Acclimatory responses to elevated CO₂ were enhanced in N-deficient plants. With N supply, the acclimatory responses were less pronounced in lower canopy leaves relative to the flag leaf. Additional N did not increase the fraction of shoot N allocated to the flag and penultimate leaves. The decrease in photosynthetic capacity in both upper-sunlit and lower-shaded leaves in elevated CO₂ was associated with a decrease in N contents in above-ground organs and with lower N partitioning to leaves. A single relationship of N per unit leaf area to the transpiration rate accounted for a significant fraction of the variation among sun-lit and shaded leaves, growth CO₂ level and N supply. We conclude that reduced stomatal conductance and transpiration can decrease plant N, leading to acclimation to CO₂ enrichment.     

Pea plant responsiveness under elevated [CO2] is conditioned by the N source (N2 fixation versus NO3− fertilization)

The main goal of this study was to test the effect of [CO₂] on C and N management in different plant organs (shoots, roots and nodules) and its implication in the responsiveness of exclusively N₂-fixing and NO₃⁻-fed plants. For this purpose, exclusively N₂-fixing and NO₃⁻-fed (10 mM) pea (Pisum sativum L.) plants were exposed to elevated [CO₂] (1000 μmol mol⁻¹ versus 360 μmol mol⁻¹ CO₂). Gas exchange analyses, together with carbohydrate, nitrogen, total soluble proteins and amino acids were determined in leaves, roots and nodules. The data obtained revealed that although exposure to elevated [CO₂] increased total dry mass (DM) in both N treatments, photosynthetic activity was down-regulated in NO₃⁻-fed plants, whereas N₂-fixing plants were capable of maintaining enhanced photosynthetic rates under elevated [CO₂]. In the case of N₂-fixing plants, the enhanced C sink strength of nodules enabled the avoidance of harmful leaf carbohydrate build up. On the other hand, in NO₃⁻-fed plants, elevated [CO₂] caused a large increase in sucrose and starch. The increase in root DM did not contribute to stimulation of C sinks in these plants. Although N₂ fixation matched plant N requirements with the consequent increase in photosynthetic rates, in NO₃⁻-fed plants, exposure to elevated [CO₂] negatively affected N assimilation with the consequent photosynthetic down-regulation.     

Temperature dependence of growth,development, and photosynthesis in maize under elevated CO2

Global atmospheric carbon dioxide concentrations (C_a) are rising. As a consequence, recent climate models have projected that global surface air temperature may increase 1.4–5.8 °C with the doubling of C_a by the end of the century. Because, changes in C_a and temperature are likely to occur concomitantly, it is important to evaluate how the temperature dependence of key physiological processes are affected by rising C_a in major crop plants including maize (Zea mays L.), a globally important grain crop with C₄ photosynthetic pathway. We investigated the temperature responses of photosynthesis, growth, and development of maize plants grown at five temperature regimes ranging from 19/13 to 38.5/32.5 °C under current (370 μmol mol⁻¹) and doubled (750 μmol mol⁻¹) C_a throughout the vegetative stages using sunlit controlled environmental chambers in order to test if the temperature dependence of these processes was altered by elevated C_a. Leaf and canopy photosynthetic rates, C₄ enzyme activities, leaf appearance rates, above ground biomass accumulation and leaf area were measured. We then applied temperature response functions (e.g., Arrhenius and Beta distribution models) to fit the measured data in order to provide parameter estimates of the temperature dependence for modeling photosynthesis and development at current and elevated C_a in maize. Biomass, leaf area, leaf appearance rate, and photosynthesis measured at growth C_a was not changed in response to CO₂ enrichment. Carboxylation efficiency and the activities of C₄ enzymes were reduced with CO₂ enrichment indicating possible photosynthetic acclimation of the C₄ cycle. All measured parameters responded to growth temperatures. Leaf appearance rate and leaf photosynthesis showed curvilinear response with optimal temperatures near 32 and 34 °C, respectively. Total above ground biomass and leaf area were negatively correlated with growth temperature. The dependence of leaf appearance rate, biomass, leaf area, leaf and canopy photosynthesis, and C₄ enzyme activities on growth temperatures was comparable between current and elevated C_a. The results of this study suggest that the temperature effects on growth, development, and photosynthesis may remain unchanged in elevated C_a compared with current C_a in maize.     

Free-air CO2 enrichment in a wheat-weed assembly – effects on water relations

In a three-year free-air CO₂ enrichment study (Mini-FACE), spring wheat associated with typical arable weeds were grown under present and elevated atmospheric carbon dioxide concentrations [CO₂] (ambient air+150 μmol mol^?1). Analyses of plant stable carbon isotope ratios and in vivo measurements of leaf gas exchange were used to describe the CO₂ effects on water relations. For most species examined elevated [CO₂] significantly increased the intrinsic water-use efficiency (A/g_s) as derived from carbon isotope analyses. In some of the species, seasonal averages of the ratio between leaf internal to atmospheric CO₂ (c_i/c_a) were found to be significantly reduced by elevated [CO₂]. Periodic leaf gas exchange measurements confirmed the increased water-use efficiency, but significant CO₂ effects became evident only over the entire season by carbon isotope analysis. In both types of analysis conducted, spring wheat was found to react significantly different from all other species examined. The relation between A/g_s and biomass production was significantly influenced by elevated [CO₂] in all three years of the study. At the end of the drier growing seasons 2003 and 2004, the soil water content tended to be increased in the CO₂ enriched plots indicating a water saving effect. These observations demonstrate the impact of elevated [CO₂] on plant water relations with a likely positive feedback leading to higher soil water availability. Due to the differences in the CO₂ responses of spring wheat compared to the weeds we suggest that rising [CO₂] may cause shifts in the species composition of crop-weed communities.     

Effects of gradual versus step increases in carbon dioxide on Plantago photosynthesis and growth in a microcosm study

This study investigated the effects of a gradual versus step increases in carbon dioxide (CO₂) on plant photosynthesis and growth at two nitrogen (N) levels. Plantago lanceolata were grown for 80 days and then treated with the ambient CO₂ (as the control), gradual CO₂ increase and step CO₂ increase as well as low and high N additions for 70 days. While [CO₂] were kept at constant 350 and 700 μmol mol⁻¹ for the ambient and step CO₂ treatments, respectively, [CO₂] in the gradual CO₂ treatment was raised by 5 μmol mol⁻¹ day⁻¹, beginning at 350 μmol mol⁻¹ and reaching 700 μmol mol⁻¹ by the end of experiment. The step CO₂ treatment immediately resulted in an approximate 50% increase in leaf photosynthetic carbon fixation at both the low and high N additions, leading to a 20–24% decrease in leaf N concentration. The CO₂-induced nitrogen stress, in return, resulted in partial photosynthetic downregulation since the third week at the low N level and the fourth week at the high N level after treatments. In comparison, the gradual CO₂ treatment induced a gradual increase in photosynthetic carbon fixation, leading to less reduction in leaf N concentration. In comparison to the ambient CO₂, both the gradual and step CO₂ increases resulted in decreases in specific leaf area, leaf N concentration but an increase in plant biomass. Responses of plant shoot:root ratio to CO₂ treatments varied with N supply. It decreased with low N supply and increased with high N supply under the gradual and step CO₂ treatments relative to that under the ambient CO₂. Degrees of those changes in physiological and growth parameters were usually larger under the step than the gradual CO₂ treatments, largely due to different photosynthetic C influxes under the two CO₂ treatments.     

Leaf photosynthesis of Haberlea rhodopensis before and during drought

Haberlea rhodopensis is a homoiochlorophyllous resurrection plant that shows a low rate of leaf net CO₂ uptake (4–6 μmol m^?2 s^?1) under saturating photosynthetic photon flux densities in air (21% O₂ and about 390 ppm CO₂). However, leaf net CO₂ uptake reaches values of 17–18 μmol m^?2 s^?1 under saturating CO₂ and light. H. rhodopensis leaves have a very low mesophyll CO₂ conductance that can partly explain the low rate of leaf net CO₂ uptake in normal air. Experimental evidences suggest that mesophyll conductance is not sensitive to temperature in the 20–35 °C range. In addition, it is shown that the (1) transpiration rate of H. rhodopensis is nearly linearly related to the vapour pressure difference between the leaf and the ambient air within the interval from 0.5 kPa to 2.5 kPa at a leaf temperature of 25 °C and (2) leaf net CO₂ uptake in normal air under saturating light does not change much with leaf temperature (between 20 °C and 30 °C). At a leaf relative water content of between 90% and 30%, the decrease of leaf net CO₂ assimilation during drought can be explained by a decrease of leaf CO₂ diffusional conductance. Accordingly the non-photochemical chlorophyll fluorescence quenching decreases only at relative water contents lower than 20%, indicating that photosynthetic activity maintains a trans-thylakoidal proton gradient over a wide range of leaf water contents. Moreover, PSII photochemistry (as estimated by the Fv/Fm ratio and the thermoluminescence B band intensity) is only affected at leaf relative water contents lower than about 20%, thus confirming that primary photosynthetic reactions are resistant to drought. Interestingly, the effect of leaf desiccation on photosynthetic capacity, measured at very high ambient CO₂ molar ratios under saturating PPFD, is identical to that observed for three non-resurrection C₃ mesophytes. This demonstrates that the photosynthetic apparatus of H. rhodopensis is not more resistant to desiccation when compared to other C₃ plants. Since the leaf area decreases by more than 50% when the leaf relative water content is reduced to about 40% during drought it is supposed, following Farrant et al. [Farrant, J.M., Vander, W.C., Lofell, D.A., Bartsch, S., Whittaker, A., 2003. An investigation into the role of light during desiccation of three angiosperms resurrection plants. Plant Cell Environ. 26, 1275–1286], that H. rhodopensis leaf cells avoid mechanical stress.     

Impact of in vitro CO2 enrichment and sugar deprivation on acclimatory responses of Phalaenopsis plantlets to ex vitro conditions

We assessed the effect of growth at either 400 μmol mol^?1 (ambient) or 1000 μmol mol^?1 (elevated) CO₂ and 0 g L^?1 (deprivation) or 30 g L^?1 (supplementation) sugar on morphological traits, photosynthetic attributes and intrinsic elements of the CAM pathway using the CAM orchid Phalaenopsis ‘Amaglade’. The growth of shoot (retarded) and root (induced) was differently affected by CO₂ enrichment and mixotrophic regime (+sugar). The Fv/Fm ratio was 14% more in CO₂-enriched treatment than at ambient level during in vitro growth. At elevated level of CO₂ and sugar treatment, the content of Chl(a + b), Chl a/b and Chl/Car was enhanced while carotenoid content remained unaltered. During in vitro growth, gas-exchange analysis indicated that increased uptake of CO₂ accorded with the increased rate of transpiration and unchanged stomatal conductance at elevated level of CO₂ under both photo- and mixotrophic growth condition. At elevated level of CO₂ and sugar deprivation, activities of Rubisco (26.4%) and PEPC (74.5%) was up-regulated. Among metabolites, the content of sucrose and starch was always higher under CO₂ enrichment during both in vitro and ex vitro growth. Our results indicate that plantlets grown under CO₂ enrichment developed completely viable photosynthetic apparatus ready to be efficiently transferred to ex vitro condition that has far-reaching implications in micropropagation of Phalaenopsis.     

Elevated CO2 alleviates negative effects of salinity on broccoli (Brassica oleracea L. var Italica) plants by modulating water balance through aquaporins abundance

In the global change scenario, increased CO₂ may favour water use efficiency (WUE) by plants. By contrast, in arid and semiarid areas, salinity may reduce water uptake from soils. However, an elevated WUE does not ensure a reduced water uptake and upon salinity this fact may constitute an advantage for plant tolerance. In this work, we aimed to determine the combined effects of enhanced [CO₂] and salinity on the plant water status, in relation to the regulation of PIP aquaporins, in the root and leaf tissues of broccoli plants (Brassica oleracea L. var Italica), under these two environmental factors. Thus, different salinity concentrations (0, 60 and 90 mM NaCl) were applied under ambient (380 ppm) and elevated (800 ppm) [CO₂]. Under non-salinised conditions, stomatal conductance (G_s) and transpiration rate (E) decreased with rising [CO₂] whereas water potential (Ψ_ω) was maintained stable, which caused a reduction in the root hydraulic conductance (L₀). In addition, PIP1 and PIP2 abundance in the roots was decreased compared to ambient [CO₂]. Under salinity, the greater stomatal closure observed at elevated [CO₂] – compared to that at ambient [CO₂] – caused a greater reduction in G_s and E and allowed plants to maintain their water balance. In addition, a lower decrease in L₀ under salt stress was observed at elevated [CO₂], when comparing with the decrease at ambient [CO₂]. Modifications in PIP1 and PIP2 abundance or their functionality in the roots is discussed. In fact, an improved water status of the broccoli plants treated with 90 mM NaCl and elevated [CO₂], evidenced by a higher Ψ_ω, was observed together with higher photosynthetic rate and water use efficiency. These factors conferred on the salinised broccoli plants greater leaf area and biomass at elevated [CO₂], in comparison with ambient [CO₂]. We can conclude that, under elevated [CO₂] and salt stress, the water flow is influenced by the tight control of the aquaporins in the roots and leaves of broccoli plants and that increased PIP1 and PIP2 abundance in these organs provides a mechanism of tolerance that maintains the plant water status.     

Growth and development of cotton (Gossypium hirsutum L.) in response to CO2 enrichment under two different temperature regimes

An increase in atmospheric CO₂ concentration ([CO₂]) together with other climate change factors could greatly affect agricultural productivity. Understanding the impact of the change in atmospheric [CO₂] in conjunction with the ongoing global change is crucial to prepare for mitigation and any adaptation for future agricultural production. The main goal of this project was to study the time-course pattern of cotton plant growth in response to [CO₂] and temperature to investigate the hypothesis that whether response to elevated [CO₂] would change at different temperatures. An experiment was conducted in the controlled-environment chambers of the Georgia Envirotron with two different day/night temperatures levels, e.g., 25/15 °C and 35/25 °C, and three CO₂ concentrations, e.g., 400, 600 and 800 μmol l^?1. The experimental design was completely randomized with four replicates (plastic containers) per treatment. Growth analysis was conducted at bi-weekly intervals during the growing season. In addition, leaf area, leaf dry mass, root dry mass, square dry mass, boll dry mass and total above dry mass per plant were also measured at each sampling. Plant traits, including plant height, number of leaves, number of squares and number of bolls were recorded weekly. The number of days to emergence, squaring, flowering and maturity were also observed. The results showed that by increasing [CO₂] to 600 μmol l^?1 total biomass increased at both temperature levels, but a further increase of [CO₂] up to 800 μmol l^?1 increased total biomass only at the temperature of 35/25 °C. Throughout the growing season, there was no significant effect of [CO₂] levels on LAI. Increasing temperature from 25/15 °C to 35/25 °C had a positive impact on LAI across all CO₂ levels (P < 0.05). Increasing CO₂ from 400 to 600 μmol l^?1 significantly increased the number of squares by 31.4%, but a further increase to 800 μmol l^?1 caused a 6.6% decrease (non-significant) in the number of squares. The interactive effects of [CO₂] and temperature indicated that at a higher temperature, CO₂ would be more beneficial as we proceed towards the end of the growing season. However, further studies are needed to really understand the interaction between higher [CO₂] and temperature levels and cultivar characteristics.     

Seasonal physiological responses and biomass growth in a bioenergy crop (<Emphasis Type="Italic">Phalaris arundinacea</Emphasis> L.) under elevated temperature and CO<Subscript>2</Subscript>, subjected to different water regimes in boreal conditions

We investigated the seasonal variability of effects of elevated temperature (+3.5°C), CO₂ elevation (700 μmol mol⁻¹) and varying water regimes (high to low water content) on physiological responses and biomass growth of reed canary grass (Phalaris arundinacea L., local field-grown cultivar) grown in a boreal environment. In controlled environment greenhouses, various physiological and growth parameters of grass, i.e., light-saturated net photosynthetic rates (P _nmax), water use efficiency (WUE) and optimal photochemical efficiency of photosystem II (F _v/F _m), and leaf area development and biomass of plant organs (leaf, stem, coarse, and fine root) were measured. During the early measurement periods, elevated temperature enhanced leaf photosynthesis and above-ground biomass of reed canary grass; however, this resulted in earlier senescence and lower biomass at the end of measurement period, compared to ambient temperature. This effect was more pronounced under water limitation. Elevated CO₂ enhanced P _nmax, WUE, and leaf area and total plant biomass (above- and below-ground) over growing season. The explanation for imbalance between stimulated photosynthesis and increase in above-ground biomass was that CO₂ enrichment causes a greater increase in the plant’s root system. The combination of elevated temperature and CO₂ slightly increases the growth of plant. Adequate water availability favored photosynthesis and biomass growth of reed canary grass. The temperature- and drought-induced stresses were partially mitigated by elevated CO₂. Other cultivars should be tested in order to identify those that are better adapted to elevated temperatures and CO₂ and variable water levels.     

Elevated atmospheric CO2 decreases oxidative stress and increases essential oil yield in leaves of Thymus vulgaris grown in a mini-FACE system

Potted one-year-old plants of Thymus vulgaris L. (thyme, Lamiaceae, C3 metabolism), were grown for three months (10 June–10 September, 2004) in a “mini-free-air-CO₂-enrichment” (“mini-FACE”) system, under 500 μmol mol^?1 and ambient concentrations of atmospheric carbon dioxide (CO₂). Compared to ambient CO₂, elevated CO₂ stimulated leaf superoxide dismutase (SOD, EC 1.15.1.1) activity only at the first sampling-time (July), followed by no variation or even a trend of decreased activity on the other two sampling-times (August and September). Under high CO₂, guaiacol peroxidase (GPX, EC 1.11.1.7) and catalase (CAT, EC 1.11.1.6) leaf activities showed no variation or drop throughout the duration of the experiment. By contrast, under elevated CO₂, leaf glutathione reductase (GR, EC 1.6.4.2) activity increased on all the sampling-times, and also a duration-dependent upward trend of glutathione (GSH) content was recorded, with this increase becoming significant – compared with ambient CO₂ – at the third sampling-time (September). Simultaneously, leaves from plants grown under high CO₂ showed a marked increase in essential oil yield, with slight increments in phenolic component and decrements in mono- and sesquiterpene components. Also, a drop in thiobarbituric acid reactive substances (TBARS) content under elevated CO₂ was displayed. Thus, in general, the results reported here point to a downregulation of leaf antioxidant enzymes under elevated CO₂, supporting the notion of reduced reactive oxygen species (ROS) formation under these circumstances. Relying instead on antioxidant-regenerating enzymes, namely GR, fairly high GSH content and essential oils, might be a ‘low cost’ life strategy for growth under elevated CO₂, not requiring synthesis/activation of energy-intensive and expensive metabolic processes.     

Increased feeding damage under elevated Co2: The case of the Russian wheat aphid

We report the results of a baseline study on the effects of Russian wheat aphid infestation on barley lines grown under ambient and elevated (450 and 550 μmol mol^− 1) CO₂ concentrations [CO₂]. Elevated CO₂ impacted on plant biomass, C:N ratios and leaf nitrogen concentrations. Visible manifestation of aphid feeding related damage was assessed by examining resultant chlorosis and leaf roll under ambient and two elevated [CO₂] levels using a control and three resistant barley host combinations. Elevated [CO₂] had a significant positive effect on the growth of the four barley lines that were not infested by the aphids. However under the same conditions aphid feeding under elevated CO₂ conditions caused very high biomass loss, which was more noticeable in experiments involving non-resistant PUMA than in the resistant barley lines. The results of this study demonstrate that CO₂ enrichment substantially increases aphid populations of RWASA1 and RWASA2 on the four barley lines investigated. Furthermore, aphid populations were higher on non-resistant PUMA than the three resistant lines and the RWASA2 biotype out-performed RWASA1 in each case. Under elevated [CO₂], aphid feeding, resulted in a significant increase in the leaf C:N ratios (as a percentage change) in most treatments, compared to levels recorded on uninfested plants. The resistant lines also showed a significant reduction in leaf nitrogen (~ 40% for PUMA and not less than 30% for the resistant STARS lines tested). C:N ratio changes and N loss correlated to [CO₂] and aphid biotype. By 28 days of infestation, most of the non-resistant PUMA line in particular showed significant irrecoverable levels of leaf chlorosis. At level 9 rating on the chlorosis scale (i.e. plant death when recovery was not possible), experiments were terminated. As aphid success is unlikely to be the sole product of [CO₂], but also of other limiting nutrients such as N, it may be worth further investigating the effect of plant quality and ultimately plant nutrition on the population growth of aphids.     

Elevated CO2 atmosphere enhances production of defense-related flavonoids in soybean elicited by NO and a fungal elicitor

Increased atmospheric pollutants including carbon dioxide (CO₂) and nitric oxide (NO) have a large impact on vegetation, with detrimental or beneficial influences on plant growth and metabolism. Here, we evaluated the effect of an elevated CO₂ atmosphere on the production of soybean defensive secondary chemicals induced by NO and a fungal elicitor. We hypothesized that an excess of carbon may alter the production of specific flavonoids that were previously shown to be induced by NO in soybean cotyledons. Pots containing soybean seeds (Glycine max [L.] Merr.) were submitted to 380 and 760 μmol mol^?1 of atmospheric CO₂ in open-top chambers. After nine days, plantlets grown under these conditions were assessed for biochemical and physiological parameters. Defense-related flavonoids were evaluated in detached cotyledon diffusates elicited with two different NO donors and with the β-glucan elicitor from Phytophthora sojae. A CO₂-enriched atmosphere stimulated initial growth, photosynthetic assimilation, and an altered C/N ratio in soybean plantlets resulting in allocation of precursors into different branches of the phenylpropanoid pathway in the cotyledons. Under elevated CO₂, the biotic elicitor caused accumulation of phytoalexins (glyceollins) as the natural end products of the phenylpropanoid pathway. In contrast, elevated CO₂ combined with NO resulted in an increase of intermediates and diverted end products (daidzein—127%, coumestrol—93%, genistein—93%, luteolin—89% and apigenin—238%) with a concomitant increase of 1.5–3.0 times in the activity of enzymes related to their biosynthetic routes. These observations point to changes in the pool of defense-related flavonoids that are related to increased carbon availability in soybeans. This may alter the responsiveness of soybean plants to pathogens when they are grown in CO₂ atmospheric concentrations close to those predicted for the upcoming several decades.     

Plasticity of rice tiller production is related to genotypic variation in the biomass response to elevated atmospheric CO2 concentration and low temperatures during vegetative growth

Appropriate resource partitioning to either production of new tillers or growth of individual tillers is a critical factor for increasing rice biomass production and facilitating adaptation to climate change. We examined the contributions of genotypic variation to the tiller number and individual tiller growth of 24 rice cultivars in response to an elevated atmospheric CO₂ concentration [CO₂] (control + 191 μmol mol⁻¹) and a low air temperature (control minus 4.7 °C) during 56 days of vegetative growth after transplanting. For all genotypes combined, biomass increased by 27% under elevated [CO₂] and decreased by 34% at low temperature, with a significant genotype × temperature interaction. The increase caused by elevated [CO₂] resulted from increased tiller number, and the decrease caused by low temperature resulted from decreased growth of individual tillers. Despite the different overall responses to elevated [CO₂] and low temperature, most of the genotypic variation in biomass at elevated [CO₂] and low temperature was explained by the responses of tiller number rather than by individual tiller growth. The genotypes with the highest biomass response to elevated [CO₂] had a smaller reduction of biomass under low temperature. These results highlight the greater importance of genotypic variation in tiller number than in individual tiller growth in the response of biomass to environmental change.