Differential responses of Arabidopsis ecotypes to cold, chilling and freezing temperatures

Arabidopsis plants show an increase in freezing tolerance in response to exposure to low nonfreezing temperatures, a phenomenon known as cold acclimation. In the present study, we evaluated the physiological and morphological responses of various Arabidopsis ecotypes to continuous growth under chilling (14°C) and cold (6°C) temperatures and evaluated their basal freezing tolerance levels. Seedlings of Arabidopsis plants were extremely sensitive to low growth temperatures: the hypocotyls and petioles were much longer and the angles of the second pair of true leaves were much greater in plants grown at 14°C than in those grown at 22°C, whereas just intermediate responses were observed under the cold temperature of 6°C. Flowering time was also markedly delayed at low growth temperatures and, interestingly, lower growth temperatures were accompanied by longer inflorescences. Other marked responses to low temperatures were changes in pigmentation, which appeared to be both ecotype specific and temperature dependent and resulted in various visual phenotypes such as chlorosis, necrosis or enhanced accumulation of anthocyanins. The observed decreases in chlorophyll contents and accumulation of anthocyanins were much more prominent in plants grown at 6°C than in those grown at 14°C. Among the various ecotypes tested, Mt‐0 plants markedly accumulated the highest levels of anthocyanins upon growth at 6°C. Freezing tolerance examination revealed that among 10 ecotypes tested, only C24 plants were significantly more sensitive to subzero temperatures. In conclusion, Arabidopsis ecotypes responded differentially to cold (6°C), chilling (14°C) and freezing temperatures, with specific ecotypes being more sensitive in particular traits to each low temperature.     

The acclimation of photosynthesis and respiration to temperature in the C3–C4 intermediate Salsola divaricata: induction of high respiratory CO2 release under low temperature

Photosynthesis in C₃–C₄ intermediates reduces carbon loss by photorespiration through refixing photorespired CO₂ within bundle sheath cells. This is beneficial under warm temperatures where rates of photorespiration are high; however, it is unknown how photosynthesis in C₃–C₄ plants acclimates to growth under cold conditions. Therefore, the cold tolerance of the C₃–C₄ Salsola divaricata was tested to determine whether it reverts to C₃ photosynthesis when grown under low temperatures. Plants were grown under cold (15/10 °C), moderate (25/18 °C) or hot (35/25 °C) day/night temperatures and analysed to determine how photosynthesis, respiration and C₃–C₄ features acclimate to these growth conditions. The CO₂ compensation point and net rates of CO₂ assimilation in cold‐grown plants changed dramatically when measured in response to temperature. However, this was not due to the loss of C₃–C₄ intermediacy, but rather to a large increase in mitochondrial respiration supported primarily by the non‐phosphorylating alternative oxidative pathway (AOP) and, to a lesser degree, the cytochrome oxidative pathway (COP). The increase in respiration and AOP capacity in cold‐grown plants likely protects against reactive oxygen species (ROS) in mitochondria and photodamage in chloroplasts by consuming excess reductant via the alternative mitochondrial respiratory electron transport chain.     

Photosynthetic downregulation in leaves of the Japanese white birch grown under elevated CO2 concentration does not change their temperature‐dependent susceptibility to photoinhibition

To determine the effects of elevated CO₂ concentration ([CO₂]) on the temperature‐dependent photosynthetic properties, we measured gas exchange and chlorophyll fluorescence at various leaf temperatures (15, 20, 25, 30, 35 and 40°C) in 1‐year‐old seedlings of the Japanese white birch (Betula platyphylla var. japonica), grown in a phytotron under natural daylight at two [CO₂] levels (ambient: 400 µmol mol^?1 and elevated: 800 µmol mol^?1) and limited N availability (90 mg N plant^?1). Plants grown under elevated [CO₂] exhibited photosynthetic downregulation, indicated by a decrease in the carboxylation capacity of Rubisco. At temperatures above 30°C, the net photosynthetic rates of elevated‐CO₂‐grown plants exceeded those grown under ambient [CO₂] when compared at their growth [CO₂]. Electron transport rates were significantly lower in elevated‐CO₂‐grown plants than ambient‐CO₂‐grown ones at temperatures below 25°C. However, no significant difference was observed in the fraction of excess light energy [(1 ? q_P)× F_v′/F_m′] between CO₂ treatments across the temperature range. The quantum yield of regulated non‐photochemical energy loss was significantly higher in elevated‐CO₂‐grown plants than ambient, when compared at their respective growth [CO₂] below 25°C. These results suggest that elevated‐CO₂‐induced downregulation might not exacerbate the temperature‐dependent susceptibility to photoinhibition, because reduced energy consumption by electron transport was compensated for by increased thermal energy dissipation at low temperatures.     

Gender-specific flowering responses to day length in the dioecious plant <Emphasis Type="Italic">Silene latifolia </Emphasis>at different temperatures

Silene latifolia Poiret is a reliable model system for studying many of the classical problems in biology because little difference in its physiological response to environmental stimuli has been found between genders. In this experiment, we studied flowering responses to day length in male and female S. latifolia plants grown at different temperatures. The primary objective was to examine whether flowering in male and female plants was differentially influenced by day length and temperature. We hypothesized that temperature would interact with day length in affecting flowering, because both genders have been found to flower in a wide range of day lengths and temperatures. Plants were grown in environmental chambers at a target temperature of 15/10 or 30/25°C (day/night). Day length was increased by half-hour intervals until all plants had flowered. Results showed that S. latifolia is a qualitative long-day plant with a critical day length of 11 h. Flowering accelerated with increasing day length until 16.5 h, when all plants flowered. Males and females differed in relative flowering at different day lengths, but to a greater extent at high than at low temperature. This study demonstrated that flowering of male and female S. latifolia respond differently to day length at different temperatures. A more uniform experimental protocol, especially in controlled environments, is called for to make this model system a more useful tool in biological studies.     

Brown Spot of Rice is Affected by Photon Irradiance and Temperature

Brown spot, caused by Bipolaris oryzae, is one of the most destructive diseases in rice. In this study, the effect of photon irradiance and temperature on brown spot development was evaluated. The concentration of total soluble sugars (fructose, glucose and sucrose) in rice leaves was also evaluated. Rice plants of cv. ‘Oochikara’ were inoculated with B. oryzae and kept in a greenhouse [20 ± 2°C (night time) and 35 ± 2°C (day time), ≈ 1000 μmol photons/m²/s] or two different mist chambers (25 or 32 ± 2°C, ≈ 15 μmol photons/m²/s at the top canopy). Plants kept in a mist chamber at 32 ± 2°C, under low photon irradiance, showed reduced incubation period (IP) and increase in the rate of lesion expansion. Brown spot severity in rice leaves was 67.8% at 32 ± 2°C, 27.8% at 25 ± 2°C and 11.4% under greenhouse conditions. The highest brown spot severity was found on plants grown under low photon irradiance, in which soluble sugar concentrations were lowest, suggesting that disease development was boosted under these particular growing conditions. Based on the results of this study, a continuous high temperature and low photon irradiance, in the presence of high relative humidity, and low soluble sugars contribute to an increase in brown spot development.     

Phytophthora cryptogea root rot of tomato in rock woo] nutrient culture. II. Effect of root zone temperature on infection, sporulation and symptom development

The effect of root-zone temperature on Phytophthora cryptogea root rot was studied in tomato cv. Counter grown under winter and summer conditions in rockwool culture. A nutrient temperature of 25°C resulted in increased root initiation and growth, higher in winter-grown than in summer-grown plants. Rhizosphere zoospore populations were greatly reduced at 25°C and above. Growth of P. cryptogea in vitro was optimal between 20°C and 25°C and completely suppressed at 30°C. Encystment was enhanced by increased temperatures above 20°C. Zoospore release in vitro occurred in cultures maintained at constant temperatures in the absence of the normal chilling stimulus. Optimal release was at 10°C; no zoospores were released at 30°C. Inoculated, winter-grown tomato plants maintained at 15°C developed acute aerial symptoms and died after 21 days. Comparable plants grown at a root-zone temperature of 25°C remained symptomless for the 3-months duration of the experiment. Summer-grown infected plants at the higher root temperature wilted but did not die. Enhanced temperature was ineffective as a curative treatment in summer-grown plants with established infection. Aerial symptoms of Phytophthora infection are seen as a function of the net amount of available healthy root. With high root zone temperatures this is determined by new root production and decreased inoculum and infection.     

Photosynthetic performance at low temperature of Bouteloua gracilis Lag., a high-altitude C4 grass from the Rocky Mountains, USA

The mechanisms controlling the photosynthetic performance of C₄ plants at low temperature were investigated using ecotypes of Bouteloua gracilis Lag. from high (3000 m) and low (1500 m) elevation sites in the Rocky Mountains of Colorado. Plants were grown in controlled‐environment cabinets at a photon flux density of 700 μ mol m^?2 s^?1 and day/night temperatures of 26/16 °C or 14/7 °C. The thermal response of the net CO₂ assimilation rate (A) was evaluated using leaf gas‐exchange analysis and activity assays of ribulose‐1,5‐bisphosphate carboxylase/oxygenase (Rubisco), phosphoenolpyruvate carboxylase (PEPCase) and pyruvate,orthophosphate dikinase (PPDK). In both ecotypes, a reduction in measurement temperature caused the CO₂‐saturated rate of photosynthesis to decline to a greater degree than the initial slope of A versus the intercellular CO₂ response, thereby reducing the photosynthetic CO₂ saturation point. As a consequence, A in normal air was CO₂‐saturated at sub‐optimal temperatures. Ecotypic variation was low when grown at 26/16 °C, with the major difference between the ecotypes being that the low‐elevation plants had higher A; however, the ecotypes responded differently when grown at cool temperature. At temperatures below the thermal optimum, A in high‐elevation plants grown at 14/7 °C was enhanced relative to plants grown at 26/16 °C, while A in low‐elevation plants grown at 14/7 °C was reduced compared to 26/16 °C‐grown plants. Photoinhibition at low growth temperature was minor in both ecotypes as indicated by small reductions in dark‐adapted F_v/F_m. In both ecotypes, the activity of Rubisco was equivalent to A below 17 °C but well in excess of A above 25 °C. Activities of PEPCase and PPDK responded to temperature in a similar proportion relative to Rubisco, and showed no evidence for dissociation that would cause them to become principal limitations at low temperature. Because of the similar temperature response of Rubisco and A, we propose that Rubisco is a major limitation on C₄ photosynthesis in B. gracilis below 17 °C. Based on these results and for theoretical reasons associated with how C₄ plants use Rubisco, we further suggest that Rubisco capacity may be a widespread limitation upon C₄ photosynthesis at low temperature.     

Dynamic photo-inhibition and carbon gain in a C4 and a C3 grass native to high latitudes

C₄ plants are rare in the cool climates characteristic of high latitudes and altitudes, perhaps because of an enhanced susceptibility to photo‐inhibition at low temperatures relative to C₃ species. In the present study we tested the hypothesis that low‐temperature photo‐inhibition is more detrimental to carbon gain in the C₄ grass Muhlenbergia glomerata than the C₃ species Calamogrostis Canadensis. These grasses occur together in boreal fens in northern Canada. Plants were grown under cool (14/10 °C day/night) and warm (26/22 °C) temperatures before measurement of the light responses of photosynthesis and chlorophyll fluorescence at different temperatures. Cool growth temperatures led to reduced rates of photosynthesis in M. glomerata at all measurement temperatures, but had a smaller effect on the C₃ species. In both species the amount of xanthophyll cycle pigments increased when plants were grown at 14/10 °C, and in M. glomerata the xanthophyll epoxidation state was greatly reduced. The detrimental effect of low growth temperature on photosynthesis in M. glomerata was almost completely reversed by a 24‐h exposure to the warm‐temperature regime. These data indicate that reversible dynamic photo‐inhibition is a strategy by which C₄ species may tolerate cool climates and overcome the Rubisco limitation that is prevalent at low temperatures in C₄ plants.     

Cold hardiness and sugar content in photo‐insensitive individuals of the cotton bollworm Helicoverpa armigera

Abstract A proportion of Helicoverpa armigera collected from fields in Okayama Prefecture (Western Japan; 34.6°N, 134.1°E) does not enter diapause when reared under a short days at 20 °C during the larval stages. However, diapause in such photo‐insensitive individuals can be induced when they are reared at moderately low temperatures, such as 15 °C, regardless of photoperiod. To determine whether such photo‐insensitive individuals can survive overwintering in fields, the present study compares the cold hardiness and sugar content between nondiapausing and diapausing pupae of photo‐insensitive individuals selected over several generations at 20 °C under a short day photoperiod (LD 10 : 14 h). Diapausing and nondiapausing pupae are obtained under the short days by rearing at 15 and 20 °C, respectively, during larval and pupal stages. These pupae are stepwise acclimated at a reduction of 5 °C every 5 days to 0 °C. Maximum survival periods of nondiapausing and diapausing pupae at 0 °C are approximately 30 and 90 days, respectively. Trehalose content in diapausing pupae increases, reaches a maximum level (1.95 mg 100 mg^?1 in males and 2.1 mg 100 mg^?1 in females) 28 days after exposure to 0 °C and then decreases. On the other hand, glucose content in diapausing pupae increases (maximum level: 0.32 mg 100 mg^?1 in males and 0.21 mg 100 mg^?1 in females) with decreasing trehalose content 42 days after exposure to 0°C. The decrease in trehalose content and the increase in glucose content may be linked to termination of diapause in H. armigera. These results suggest that, in Japan, the photo‐insensitive individuals can only survive in the mild winters of southern regions, and not in the severe winters of northern regions.     

Comparison of cold hardiness and sugar content between diapausing and nondiapausing pupae of the cotton bollworm, Helicoverpa armigera (Lepidoptera: Noctuidae)

Abstract. To understand overwintering of the cotton boll worm Helicoverpa armigera, cold hardiness and sugar content are compared between diapausing and nondiapausing pupae. Diapausing and nondiapausing pupae reared at 20 °C under short and long photoperiods are acclimatized with a reduction of 5 °C per 5 days to 0 °C. When the acclimation temperature reaches 0 °C, the survival of diapausing pupae is assessed. The survival gradually decreases as the period of treatment progresses and approximately half survive for 112 days. However, nondiapausing pupae survive only 14 days after exposure to 0 °C. The surpercooling points of nondiapausing, diapausing and acclimatized pupae are approximately −17 °C. The major sugars contained in pupae are trehalose and glucose. Even though trehalose contents in diapausing pupae (initial level: 0.6 mg 100 mg⁻¹ fresh weight) increase significantly during cold acclimation and continue increasing until 58 days after exposure to 0 °C (maximum level: 1.8 mg 100 mg⁻¹), glucose is maintained at low levels (0.02 mg 100 mg⁻¹) for 56 days at 0 °C. However, glucose contents increase (maximum level: 0.8 mg 100 mg⁻¹) with decreasing contents of trehalose 84 days after exposure to 0 °C. Glycogen content gradually decreases during cold acclimation. When nondiapausing pupae are acclimatized with a reduction of 5 °C per 5 days to 5 °C from the beginning of pupation until the eyespots move, trehalose content increases (maximum level: 1.0 mg 100 mg⁻¹). Glucose contents in nondiapausing pupae increase before eclosion (0.09 mg 100 mg⁻¹). From these results, diapausing pupae of H. armigera can overwinter in regions where average winter temperatures are higher than 0 °C, but nondiapausing pupae cannot.     

Low-temperature photosynthetic performance of a C4 grass and a co-occurring C3 grass native to high latitudes

The photosynthetic performance of C₄ plants is generally inferior to that of C₃ species at low temperatures, but the reasons for this are unclear. The present study investigated the hypothesis that the capacity of Rubisco, which largely reflects Rubisco content, limits C₄ photosynthesis at suboptimal temperatures. Photosynthetic gas exchange, chlorophyll a fluorescence, and the in vitro activity of Rubisco between 5 and 35 °C were measured to examine the nature of the low‐temperature photosynthetic performance of the co‐occurring high latitude grasses, Muhlenbergia glomerata (C₄) and Calamogrostis canadensis (C₃). Plants were grown under cool (14/10 °C) and warm (26/22 °C) temperature regimes to examine whether acclimation to cool temperature alters patterns of photosynthetic limitation. Low‐temperature acclimation reduced photosynthetic rates in both species. The catalytic site concentration of Rubisco was approximately 5.0 and 20 µmol m^?2 in M. glomerata and C. canadensis, respectively, regardless of growth temperature. In both species, in vivo electron transport rates below the thermal optimum exceeded what was necessary to support photosynthesis. In warm‐grown C. canadensis, the photosynthesis rate below 15 °C was unaffected by a 90% reduction in O₂ content, indicating photosynthetic capacity was limited by the capacity of P_i‐regeneration. By contrast, the rate of photosynthesis in C. canadensis plants grown at the cooler temperatures was stimulated 20–30% by O₂ reduction, indicating the P_i‐regeneration limitation was removed during low‐temperature acclimation. In M. glomerata, in vitro Rubisco activity and gross CO₂ assimilation rate were equivalent below 25 °C, indicating that the capacity of the enzyme is a major rate limiting step during C₄ photosynthesis at cool temperatures.     

Evaluation of cold stress of young industrial chicory (<Emphasis Type="Italic">Cichorium intybus</Emphasis> L.) by chlorophyll <Emphasis Type="Italic">a</Emphasis> fluorescence imaging. II. Dark relaxation kinetics

Industrial chicory, Cichorium intybus L., has rather poor early vigour under the typical early spring morning conditions of low temperatures and high light intensity. Screening tools are being developed to assess the cold tolerance/sensitivity of young industrial chicory plants under these conditions. Refinement of such tools requires better understanding of the plants’ physiological responses. In this paper we discuss the effects of growth temperature (GT), measurement temperature (MT), and measuring light intensity (ML) on the relaxation of the Kautsky curve. We chose the chicory variety ‘Hera’, as it is known to possess a good average early vigour. Young plants of the variety ‘Hera’ were grown at three temperatures (GT): 16°C (reference), 8°C (intermediate), and 4°C (cold stress). The dark relaxation kinetics were analyzed at different light intensities (ML) in combination with different measurement temperatures (MT). The three components of the nonphotochemical quenching process (NPQ_E, NPQ_T, and NPQ_I) were determined. NPQ_E was not affected by GT but was significantly affected by MT and ML. NPQ_T and NPQ_I were affected by all factors and their interactions. An acclimation effect for plants grown at low GT was detected. Acclimation resulted in lower NPQ_T and NPQ_I values. The halftime of the inhibition depending on NPQ (NPQ_I) was not affected by any of the factors investigated. Based on the data generated, we conclude that NPQ_I is a valuable parameter for screening the cold sensitivity of young industrial chicory plants.     

Supraoptimal Temperature Effects upon Agrostis palustris

Agrostis palustris turfs cut weekly at 1.3 cm were subjected to successive four-week periods with day-night temperature regimes of 20–10, 25–15, 30–20, 35–25 and 40–30°C. Plants grown at 40–30°C exhibited a growth character distinctly different from those grown at 20–10°C. They were more upright and bristle-like in growth habit. The percentage dry weight of leaf blade tissue increased 67% and weight per unit area increased 53% between 20–10 and 40–30°C. Reduced leaf blade width was noted first at 30–20°C while leaf blade length reduction first occurred at 35–25°C. Weekly yields were significantly reduced at the supraoptimal temperature regimes of 35–25 and 40–30°C. Chlorophyll content was lowest at 20–10 and 40–30°C, the lowest and highest temperature regimes studied. Shoot density appeared to decrease under the 35–25°C regime, but no dead plants were observed. The apparent decrease in shoot density was attributed to the upright growth habit. Density decreased at 40–30°C upon death of individual plants. A community of grass plants maintained as a turf was found to change in form quite rapidly in response to temperature.     

Quantifying and Modeling the Influence of Temperature on Growth and Reproductive Development of Sesame

Ambient temperatures are major factors regulating the growth rates, yields, and geographical distribution of crop species. The cultivation of sesame (Sesamum indicum L.) is expanding with the rising demand in regions where it is not traditionally grown, and sub-optimal yields due to extremely low or high temperatures could occur. Currently literature lacks information on the temperature responses of sesame growth. An experiment was conducted to quantify the effects of different temperatures on vegetative growth and reproductive development of sesame, and to estimate its cardinal temperature limits (T_opt; T_min; T_max). Plants were subjected to six different day/night temperature treatments of 40/32, 36/28, 32/24, 28/20, and 20/12 °C using walk-in growth chambers. Vegetative growth of sesame was sensitive to low temperatures (<?15 °C), but tolerant of high temperatures. The cardinal temperature limits of 15.7 °C (T_min), 27.3 °C (T_opt), and 44.6 °C (T_max) were observed for rate of biomass accumulation. Sesame reached the flowering stage under moderate to high temperature conditions; however, reproductive yields progressively declined above 25 °C, and no seed yields were obtained beyond 33 °C. The estimated temperature limits could be employed to develop crop models for simulating management and adaptation strategies of sesame under current and future climate scenarios, and adaptation to regions where the crop is not currently grown. Future research should focus on understanding factors controlling the temperature tolerance of reproductive development in sesame, to provide a broader geographical adaptation.

     

List of members August, 1962

We investigated the acclimation of Chondrus crispus to growth at 5°C and 20°C in the laboratory. We were specifically interested in the responses of light-limited photosynthesis to temperature and the effects of short-term thermal changes (of the order of minutes). Thermal acclimation to constant temperatures over 3–4 weeks had significant effects on the light-use characteristics of this species such that in comparison with those grown at 5°C, 20°C-grown plants had higher concentrations of chlorophyll a and total phycobilins, which were associated with larger photosynthetic unit sizes. Plants grown at the higher temperature had greater photosynthetic efficiencies (α) and higher rates of light-limited photosynthesis at a given photon flux density than did plants acclimated to 5°C. Plants acclimated to 20°C were less sensitive to short-term temperature changes than were 5°C-acclimated plants. These results are discussed in terms of (1) the effects of growth temperature on light harvesting and (2) the implications of exposure to constant temperature for short-term thermal responses.     

Physiological responses of Opuntia ficus-indica to growth temperature

The influences of various day/night air temperatures on net CO₂ uptake and nocturnal acid accumulation were determined for Opuntia ficus-indica, complementing previous studies on the water relations and responses to photosynthetically active radiation (PAR) for this widely cultivated cactus. As for other Crassulacean acid metabolism (CAM) plants, net nocturnal CO₂ uptake had a relatively low optimal temperature, ranging from 11°C for plants grown at day/night air temperatures of 10°C/0°C to 23°C at 45°C/35°C. Stomatal opening, which occurred essentially only at night and was measured by changes in water vapor conductance, progressively decreased as the measurement temperature was raised. The CO₂ residual conductance, which describes chlorenchyma properties, had a temperature optimum a few degrees higher than the optimum for net CO₂ uptake at all growth temperatures. Nocturnal CO₂ uptake and acid accumulation summed over the whole night were maximal for growth temperatures near 25°C/15°C, CO₂ uptake decreasing more rapidly than acid accumulation as the growth temperature was raised. At day/night air temperatures that led to substantial nocturnal acid accumulation (25°C/15°C.). 90% saturation of acid accumulation required a higher total daily PAR than at non-optimal growth temperatures (10°C/0°C and 35°C/25°C). Also, the optimal temperature of net CO₂ uptake shifted downward when the plants were under drought conditions at all three growth temperatures tested, possibly reflecting an increased fractional importance of respiration at the higher temperatures during drought. Thus, water status, ambient PAR, and growth temperatures must all be considered when predicting the temperature response of gas exchange for O. ficus-indica and presumably for other CAM plants.     

Expression of cold-inducible genes and frost hardiness in the crown meristem of young barley (Hordeum vulgare L. cv. Igri) plants grown in different environments

The purpose of this work was to examine environmental control of expression, at the mRNA level, of cold-inducible genes and to test the relationship of the expression of the genes to cold acclimation. Barley plants (Hordeum vulgare L. cv. Igri) at the three- to four-leaf stage were (a) grown in different temperature environments between 20/15°C and +4/-4°C or (b) transferred between 20/15°C and 6/2°C or (c) grown under drought or nutrient stress conditions. Frost hardiness (using a regrowth method) and mRNA levels for three cold-induced genes, blt4-9, blt14 and blt101, from meristematic crown tissue (vegetative shoot meristem plus subtending stem and associated root initials) were measured. Hardiness and levels of blt4-9, blt14 and blt101 mRNAs increased with lower growth temperatures, below a maximum inductive temperature. Prior temperature environment and plant age affected the rate of change in mRNA levels of these genes in response to a change of temperature environment. Hardiness was strongly correlated with mRNA levels of these genes in plants grown in different temperature environments. This correlation did not extend to plants exposed to drought or nutrient stresses. Implications are drawn for plant responses to a warmer climate.     

An analysis of photosynthetic response and adaptation to temperature in higher plants: temperature acclimation in the desert evergreen Nerium oleander L*

Abstract. Factors underlying the process of photosynthetic acclimation to temperature were investigated for the shrub Nerium oleander L. Ramets of a single clone were grown under day/night temperature regimes of 20°C/15°C or 45°C/32°C. Plants grown at the lower temperature regime possessed rates of photosynthesis twice that of the high-temperature grown plants when CO₂ fixation was measured at 20°C. In contrast, the plants grown at the high-temperature regime had twice the rate of CO₂ fixation of the 20°C/l 5°C-grown plants at a measurement temperature of 45° C. It was determined that the ability to acclimate to changes in temperature regime was present in fully mature leaves. A reciprocal transfer of plants between the two growth regimes resulted in the appearance of the CO₂ fixation characteristics appropriate to the new growth temperature after 12–14d. The response of CO₂ fixation to light, temperature, and CO₂ partial pressure and the temperature responses of soluble and membrane-bound photosynthetic enzyme systems were analysed to determine which components might be responsible for the superior photosynthetic performance of the 20°C/I5°C-grown plants at 20°C, and the enhanced high-temperature stability of the 45°C/32°C plants. The measured photosynthetic capacity of the 20°C/15°C plants could not be attributed to gross morphological, stomatal, or other physical changes, or to a general increase in the concentration of components of the photosynthetic process. Only a single enzyme, Fru-P₂ phosphatase, was affected to an extent similar to that of photosynthesis. The enhanced thermal stability of the 45°C/32°C plants may be attributed primarily to an enhanced stability of the chloroplast membrane-bound enzymatic activities and the stability of the photosynthetic carbon metabolism enzymes which require lighl for activation.     

Evaluation of cold stress of young industrial chicory (<Emphasis Type="Italic">Cichorium intybus</Emphasis> L.) plants by chlorophyll <Emphasis Type="Italic">a</Emphasis> fluorescence imaging. I. Light induction curve

Industrial chicory, Cichorium intybus L., is cultivated for the production of inulin. Most varieties of industrial chicory exhibit rather poor early growth, which limits further yield improvements in their European cultivation area. The poor early growth could be due to suboptimum adaptation of the gene pool to growth at low temperatures, sometimes in combination with high light intensities, which is typical of early-spring mornings. We have used chlorophyll (Chl) a fluorescence to evaluate the response of young plants of the cultivar ‘Hera’ to low temperatures and high light intensities. Plants were grown at three temperatures: 16°C (reference), 8°C (intermediate), and 4°C (cold stress). Light-response measurements were carried out at different light intensities in combination with different measurement temperatures. Parameters that quantify the photosystem II (PSII) operating efficiency (including PSII maximum efficiency and PSII efficiency factor) and nonphotochemical quenching (NPQ) are important to evaluate the stress in terms of severity, the photosynthetics processes affected, and acclimation to lower growth temperatures. The results clearly demonstrate that in young industrial chicory plants the photosynthetic system adapts to lower growth temperatures. However, to fully understand the plant response to the stresses studied and to evaluate the long-term effect of the stress applied on the growth dynamics, the subsequent dark relaxation dynamics should also be investigated.