Time course of photosynthetic temperature acclimation in Carex eleocharis Bailey

Abstract Photosynthetic temperature acclimation in Carex eleocharis has been demonstrated in a previous study in which warm grown (35/15°C) plants were shown to have photosynthetic temperature optima approximately 14°C higher than cool grown (20/15°C) plants (Monson, Littlejohn & Williams, 1983). The current study examined the time course of this acclimation by determining photo-synthetic temperature optima as a function of time, of cool grown plants moved to warm growing conditions. Leaves which had developed under cool conditions were capable of an upward adjustment of 6–8°C of their optimum photosynthetic temperature within a time span of 6–14 d. For greatest photosynthetic temperature acclimation it was necessary for leaves to form and develop entirely under warm conditions. These leaves exhibited a 14–15°C upward adjustment of their optimum temperature for photosynthesis within 20–31 d since moving plants from cool to warm growing conditions. Thus, the time course of this acclimation is of short enough duration to be significant during the growing season and presumably contributes toward the ability of this species to maintain active growth during the cool and warm portions of the growing season. It is also noted that the plant with its capacity to form new leaves, has a much wider acclimation capacity than any single leaf.     

Temperature relations of photosynthetic response in populations of Verbascum thapsus L.

Summary Seedlings representative of Verbascum thapsus L. populations from thermally diverse habitats were grown under uniform, controlled conditions. The plants were used to obtain temperature response curves for net photosynthesis over a range of 15–40°C. In general, all experimental plants exhibited similar rates of net photosynthesis at 20, 25, 30, and 35°C. Plants representative of cool habitat populations (high-latidude and high-altitude) had greatest rates of net photosynthesis at the lower temperatures and much lower rates at 40°C. Plants representative of warm habitat populations (low-latitude and low-altitude) exhibited rates of net photosynthesis at 40°C which were nearly twice those of plants representative of cool habitat populations. Carbon dioxide transfer resistances are discussed with reference to plant control of photosynthesis at different temperatures. Patterns of photosynthesis and resistance response among plants representative of different habitats suggest ecotypic variation has occurred only to a very limited extent. Therefore, the patterns exhibited by experimental plants suggest that Verbascum thapsus' success in a number of diverse sites is related to the ability of all members of the species to photosynthesize over a broad range of temperatures.     

A field study of photosynthetic temperature acclimation in Carex eleocharis Bailey

Abstract. Seasonal patterns in photosynthetic temperature acclimation and growth were investigated in the sedge, Carex eleocharis Bailey, a species which has demonstrated a marked capacity for shifts in the photosynthetic temperature optimum in previous growth chamber studies. The seasonal production of new leaves was 90% complete by the earliest study date, June 3. Shifts in the photosynthetic temperature optimum of 10°C (from 15 to 25°C) were observed during the months of June and July. These results indicate that in situ acclimatory adjustments in C. eleocharis occur in existing leaf tissue, rather than new leaves which are produced as the season progresses. Despite the 10°C increase in the temperature optimum, mean mid-day leaf temperatures were higher than the optimum throughout the summer. A broad temperature response appeared to be more important than the acclimation adjustments in maintaining near-maximum photosynthesis rates during the mid-day period. Seasonal shifts in the photosynthetic temperature optimum were not as great as those previously observed in growth chamber studies. This discrepancy arises because of the capacity for growth chamber grown plants to produce new leaves with temperature response characteristics closely tuned to the growth temperature regime. In field-grown plants the production of 90% of the leaves during the cool portion of the season places limitations on the potential for acclimation to the warmer midsummer temperatures.     

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.     

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.     

Photosynthesis and cannabinoid content of temperate and tropical populations of Cannabis sativa

Four populations of Cannabis sativa L. grown from seeds collected in Panama, Jamaica, Nepal, and east central Illinois were grown under controlled conditions in growth chambers. One set was grown under warm conditions (32° day and 23° night) and the other set was grown under lower temperatures (23° day and 16° night). CO₂ exchange and transpiration were examined under various temperatures and light intensities. Observations on growth, and analyses for chlorophyll and Δ₁THC (tetrahydrocannabinol) content were made. Under warm growth conditions, the central Illinois population had the highest photosynthetic rate at all temperatures investigated. The Nepal population had intermediate rates, while the Jamaica and the Panama populations had the lowest rate. The Jamaica and Panama populations had insignificant changes in photosynthetic response to changes in temperatures between 15° and 30°. Under cool growing conditions the central Illinois population had the highest rate of photosynthesis with a definite peak at 25°. Nepal plants had intermediate rates of photosynthesis, while the Panama and Jamaica populations had the lowest rate. Differences in chlorophyll and drug content were also significant between these populations. From these data it is suggested that the four populations can be grouped into different ecotypes genetically adapted to their respective environments.     

Response of stomatal resistance and photosynthesis to night temperature in Populus deltoides

Summary Ramets from stem cuttings of three populations of Populus deltoides Bartr. from Wisconsin, Illinois, and Louisiana representing a latitudinal gradient were grown in pots outdoors at Urbana, Illinois and brought indoors for growth chamber studies. Leaf resistance and photosynthetic response to low night temperatures of 4° and 10° C were determined relative to 20° C controls for plants measured over one growing season. Plants from Louisiana, where nights are warm, reacted to cool nights of 4° and 10° C by opening their stomata slower upon illumination the following day than those from farther north where nights are cooler. The optimum night temperature for rate of opening was lower in the Wisconsin population than in populations from farther south. The Wisconsin population showed more ideal homeostasis of photosynthesis at different temperatures than the southern population which exhibited greater plasticity. No seasonal differences in these relationships were apparent other than at the time of leaf senescence.As plants approached senescence, which occurred earliest in the Wisconsin population, leaf resistance increased and photosynthesis declined, but stomata still retained their functional ability to respond to changes in night temperature. The change in leaf resistance, noted in the Wisconsin population, was related more to closure of lower-leaf surface stomata than upper. Only the Louisiana population had significantly more stomata on the lower than upper leaf surface.     

Differences in photosynthetic characteristics among northern and southern C4 plants

Both responses to short-term changes of temperature and to chilling under high light were analyzed in populations of Echinochloa crus-galli var. crus-galli (L.) Beauv. from Québec. North Carolina and Mississippi to improve the understanding of C₄ photosynthesis at low temperature. Comparison also included plants of Eleusine indica (L.) Gaertn. from Mississippi to provide for differences among species and populations. Plants were grown at two thermoperiods (28/22°C, 21/15°C). After transfer from cool (21/15°C) to warm (28/22°C) growth conditions, Echinochloa from Mississippi achieved the highest photosynthetic rates. Plants from Québec maintained the highest rates of CO₂ uptake upon transfer to cool conditions. Exposure to 7°C for 3 days at a photon fluence rate of 1000 μmol m−²s−¹ resulted in a reduction in the growth rates of all populations. This reduction was paralleled by a decrease in net photosynthesis and in stomatal conductance. Following chilling under hight light, the reduction in growth parameters was less important for plants from Québec than for the other populations. It suggests that, among other characteristics, northern plants had developed a certain tolerance to chilling under light.     

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.     

Temperature responses of photosynthesis and respiration in <Emphasis Type="Italic">Populus</Emphasis><Emphasis Type="Italic">balsamifera</Emphasis> L.: acclimation versus adaptation

To examine the role of acclimation versus adaptation on the temperature responses of CO₂ assimilation, we measured dark respiration (R _n) and the CO₂ response of net photosynthesis (A) in Populus balsamifera collected from warm and cool habitats and grown at warm and cool temperatures. R _n and the rate of photosynthetic electron transport (J) are significantly higher in plants grown at 19 versus 27°C; R _n is not affected by the native thermal habitat. By contrast, both the maximum capacity of rubisco (V _cmax) and A are relatively insensitive to growth temperature, but both parameters are slightly higher in plants from cool habitats. A is limited by rubisco capacity from 17–37°C regardless of growth temperature, and there is little evidence for an electron-transport limitation. Stomatal conductance (g _s) is higher in warm-grown plants, but declines with increasing measurement temperature from 17 to 37°C, regardless of growth temperature. The mesophyll conductance (g _m) is relatively temperature insensitive below 25°C, but g _m declines at 37°C in cool-grown plants. Plants acclimated to cool temperatures have increased R _n/A, but this response does not differ between warm- and cool-adapted populations. Primary carbon metabolism clearly acclimates to growth temperature in P. balsamifera, but the ecotypic differences in A suggest that global warming scenarios might affect populations at the northern and southern edges of the boreal forest in different ways.     

The response of the high altitude C(4) grass Muhlenbergia montana (Nutt.) A.S. Hitchc. to long- and short-term chilling.

The acclimation of C(4) photosynthesis to low temperature was studied in the montane grass Muhlenbergia montana in order to evaluate inherent limitations in the C(4) photosynthetic pathway following chilling. Plants were grown in growth cabinets at 26 degrees C days, but at night temperatures of either 16 degrees C (the control treatment), 4 degrees C for at least 28 nights (the cold-acclimated treatment), or 1 night (the cold-stress treatment). Below a measurement temperature of 25 degrees C, little difference in the thermal response of the net CO(2) assimilation rate (A) was observed between the control and cold-acclimated treatment. By contrast, above 30 degrees C, A in the cold-acclimated treatment was 10% greater than in the control treatment. The temperature responses of Rubisco activity and net CO(2) assimilation rate were similar below 22 degrees C, indicating high metabolic control of Rubisco over the rate of photosynthesis at cool temperatures. Analysis of the response of A to intercellular CO(2) level further supported a major limiting role for Rubisco below 20 degrees C. As temperature declined, the CO(2) saturated plateau of A exhibited large reductions, while the initial slope of the CO(2) response was little affected. This type of response is consistent with a Rubisco limitation, rather than limitations in PEP carboxylase capacity. Stomatal limitations at low temperature were not apparent because photosynthesis was CO(2) saturated below 23 degrees C at air levels of CO(2). In contrast to the response of photosynthesis to temperature and CO(2) in plants acclimated for 4 weeks to low night temperature, plants exposed to 4 degrees C for one night showed substantial reduction in photosynthetic capacity at temperatures above 20 degrees C. Because these reductions were at both high and low CO(2), enzymes associated with the C(4) carbon cycle were implicated as the major mechanisms for the chilling inhibition. These results demonstrate that C(4) plants from climates with low temperature during the growing season can fully acclimate to cold stress given sufficient time. This acclimation appears to involve reversal of injury to the C(4) cycle following initial exposure to low temperature. By contrast, carbon gain at low temperatures generally appears to be constrained by the carboxylation capacity of Rubisco, regardless of acclimation time. The inability to overcome the Rubisco limitation at low temperature may be an inherent limitation restricting C(4) photosynthetic performance in cooler climates.     

Photoinhibition of photosynthesis in intact kiwifruit (Actinidia deliciosa) leaves: effect of growth temperature on photoinhibition and recovery

Intact leaves of kiwifruit (Actinidia deliciosa (A. Chev.) C.F. Liang et A.R. Ferguson) from plants grown in a range of controlled temperatures from 15/10 to 30/25°C were exposed to a photon flux density (PFD) of 1500 μmol·m⁻²·s⁻¹ at leaf temperatures between 10 and 25°C. Photoinhibition and recovery were followed at the same temperatures and at a PFD of 20 μmol·m⁻²·s⁻¹, by measuring chlorophyll fluorescence at 77 K and 692 nm, by measuring the photon yield of photosynthetic O₂ evolution and light-saturated net photosynthetic CO₂ uptake. The growth of plants at low temperatures resulted in chronic photoinhibition as evident from reduced fluorescence and photon yields. However, low-temperature-grown plants apparently had a higher capacity to dissipate excess excitation energy than leaves from plants grown at high temperatures. Induced photoinhibition, from exposure to a PFD above that during growth, was less severe in low-temperature-grown plants, particularly at high exposure temperatures. Net changes in the instantaneous fluorescence,F ₀, indicated that little or no photoinhibition occurred when low-temperature-grown plants were exposed to high-light at high temperatures. In contrast, high-temperature-grown plants were highly susceptible to photoinhibitory damage at all exposure temperatures. These data indicate acclimation in photosynthesis and changes in the capacity to dissipate excess excitation energy occurred in kiwifruit leaves with changes in growth temperature. Both processes contributed to changes in susceptibility to photoinhibition at the different growth temperatures. However, growth temperature also affected the capacity for recovery, with leaves from plants grown at low temperatures having moderate rates of recovery at low temperatures compared with leaves from plants grown at high temperatures which had negligible recovery. This also contributed to the reduced susceptibility to photoinhibition in low-temperature-grown plants. However, extreme photoinhibition resulted in severe reductions in the efficiency and capacity for photosynthesis.     

Temperature response of photosynthesis in C3, C4, and CAM plants: temperature acclimation and temperature adaptation

Most plants show considerable capacity to adjust their photosynthetic characteristics to their growth temperatures (temperature acclimation). The most typical case is a shift in the optimum temperature for photosynthesis, which can maximize the photosynthetic rate at the growth temperature. These plastic adjustments can allow plants to photosynthesize more efficiently at their new growth temperatures. In this review article, we summarize the basic differences in photosynthetic reactions in C₃, C₄, and CAM plants. We review the current understanding of the temperature responses of C₃, C₄, and CAM photosynthesis, and then discuss the underlying physiological and biochemical mechanisms for temperature acclimation of photosynthesis in each photosynthetic type. Finally, we use the published data to evaluate the extent of photosynthetic temperature acclimation in higher plants, and analyze which plant groups (i.e., photosynthetic types and functional types) have a greater inherent ability for photosynthetic acclimation to temperature than others, since there have been reported interspecific variations in this ability. We found that the inherent ability for temperature acclimation of photosynthesis was different: (1) among C₃, C₄, and CAM species; and (2) among functional types within C₃ plants. C₃ plants generally had a greater ability for temperature acclimation of photosynthesis across a broad temperature range, CAM plants acclimated day and night photosynthetic process differentially to temperature, and C₄ plants was adapted to warm environments. Moreover, within C₃ species, evergreen woody plants and perennial herbaceous plants showed greater temperature homeostasis of photosynthesis (i.e., the photosynthetic rate at high-growth temperature divided by that at low-growth temperature was close to 1.0) than deciduous woody plants and annual herbaceous plants, indicating that photosynthetic acclimation would be particularly important in perennial, long-lived species that would experience a rise in growing season temperatures over their lifespan. Interestingly, across growth temperatures, the extent of temperature homeostasis of photosynthesis was maintained irrespective of the extent of the change in the optimum temperature for photosynthesis (T _opt), indicating that some plants achieve greater photosynthesis at the growth temperature by shifting T _opt, whereas others can also achieve greater photosynthesis at the growth temperature by changing the shape of the photosynthesis–temperature curve without shifting T _opt. It is considered that these differences in the inherent stability of temperature acclimation of photosynthesis would be reflected by differences in the limiting steps of photosynthetic rate.     

Photosynthetic Responses of Different Varieties of Wheat to High Temperature: I. EFFECT OF GROWTH TEMPERATURE ON DEVELOPMENT AND PHOTOSYNTHETIC PERFORMANCE

Both fast and slow chlorophyll fluorescence kinetics were usedto assess the differential heat sensitivity of ten wheat (Triticumaestivum L.) varieties commonly grown in northern, temperateor (sub-) tropical climate zones. No consistent differencesbetween the groups were found. Studies on the role of growthtemperature in modulating the response of photosynthesis toheat stress were carried out on two of the varieties, APU (Finnish)and K65 (Indian), the former being more sensitive to heat stress.Growth and development of these varieties were similar underboth cool (13 °C day, 10 °C night) and warm (30 °Cday, 25 °C night), regimes. The cool-grown plants exhibitedhigher rates of net CO₂ exchange than the warm-grown plantswhen expressed on a chlorophyll basis and, in both regimes,photosynthesis declined with age prior to reduction in chlorophyllcontent. Net CO₂ exchange in leaves of K65 showed greater sensitivityto short-term heat stress than APU when plants were grown underthe cool regime. Plants grown under the warm regime exhibitedan upward shift in the optimum temperature for net CO₂ exchangein both varieties, with K65 showing somewhat superior performanceat high temperature compared with APU. Stomatal aperture wasessentially unaffected by assay temperature during these measurements. Key words: CO₂ exchange, growth temperature, Triticum aestivum     

Membrane phospholipid phase separations in plants adapted to or acclimated to different thermal regimes

The phase separation temperatures of total leaf phospholipids from warm and cool climate plants were determined in order to explore the relationship of lipid physical properties to a species' thermal habitat. The separation temperatures were determined by measuring the fluorescence intensity and fluorescence polarization of liposomes labeled with the polyene fatty acid probe trans-parinaric acid. To focus on a single climatic region, Mojave Desert dicots (chiefly ephemeral annuals) were examined, with plants grown under identical conditions whenever possible. Winter active species showed lower phase separation temperatures than the summer active species. A group of warm climate annual grasses showed separation temperatures distinctly higher than those of a group of cool climate grasses, all grown from seed under the same conditions. Growth at low temperature seems correlated with (and may require) a low phase separation temperature. Winter active ephemerals appear genetically programmed to synthesize a mixture of phospholipids which will not phase separate in the usual growth conditions. When the lipids of desert perennials were examined in cool and warm seasons, there was a pronounced seasonal shift in the phase separation temperature, implying environmental influences on lipid physical properties. The relationship of these results to high and low temperature tolerance is discussed.     

A correlation between photosynthetic temperature adaptation and seasonal phenology patterns in the shortgrass prairie

Summary The temperatures at which chlorophyll fluorescence yield is substantially increased and the temperatures at which the quantum yield for CO₂ uptake is irreversibly inhibited were measured for three shortgrass prairie species. The experimental taxa include, a cool season species (Agropyron smithii), a warm season species (Bouteloua gracilis), and a species which grows throughout the cool and warm seasons (Carex stenophylla). Agropyron smithii exhibited lower high temperature damage thresholds (43°C in cool grown plants, 46°C in warm grown plants), relative to the other two species. Bouteloua gracilis exhibited the highest tolerance to high temperature, with threshold values being 44–49°C for cool grown plants and 53–55°C for warm grown plants. Carex stenophylla exhibited threshold values which were intermediate to the other two species (43–47°C for cool grown plants, and 51–53°C for warm grown plants). Seasonal patterns in the fluorescence rise temperatures of field grown plants indicated acclimation to increased temperatures in all three species. The results demonstrate a correlation between the high temperature thresholds for damage to the photosynthetic apparatus, and in situ seasonal phenology patterns for the three species.     

Warm temperature conditions restrict the sexual reproduction and vegetative growth of the spring ephemeral <Emphasis Type="Italic">Gagea lutea</Emphasis> (Liliaceae)

The responses of reproduction and growth to climate warming are important issues to predict the fate of plant populations at high latitudes. Spring ephemerals inhabiting cool-temperate forests grow better under cool conditions, but how reproductive performance is influenced by warm weather is unclear. The phenological and physiological responses of reproduction and vegetative growth to warm temperature and light conditions were evaluated in the spring ephemeral Gagea lutea. Leaf and bract physiological activities, bulb growth, and seed production were compared among reproductive plants grown in forest, open, and greenhouse (GH; warming manipulation in the open site) plots. In vitro pollen germination ability was tested under various temperatures. In the GH, leaf and bract photosynthetic activities decreased rapidly at the fruiting stage, but dark respiration rates remained high, resulting in higher carbon exhaust in warm conditions. Both leaf and bract sizes and their longevities were reduced in the GH. Annual bulb growth was largest in the forest plot and smallest in the GH plot. Pollen germination was strongly inhibited at high temperature (30 °C). Fruit and seed productions were decreased only in the GH plot. Both vegetative and reproductive activities were negatively affected by warm temperature, resulting in less vegetative growth and lower seed-set, whereas an understory habitat was beneficial for vegetative growth and showed similar seed production to an open habitat over the experimental period. Decreasing population dynamics of spring ephemerals was predicted in response to future warming climate not only by growth inhibition but also by restriction of seed production.     

Acclimation of photosynthesis to temperature in eight cool and warm climate herbaceous C3 species: Temperature dependence of parameters of a biochemical photosynthesis model

To determine how parameters of a Farquhar-type photosynthesis model varied with measurement temperature and with growth temperature, eight cool and warm climate herbaceous crop and weed species were grown at 15 and 25 °C and single leaf carbon dioxide and water vapor exchange rates were measured over the range of 15 – 35 °C. Photosynthetic parameters examined were the initial slope of the response of assimilation rate (A) to substomatal carbon dioxide concentration (C_i), A at high C_i, and stomatal conductance. The first two measurements allow calculation of V_Cmax, the maximum rate of carboxylation of ribulose bisphosphate carboxylase and J_max, the maximum rate of photosynthetic electron transport, of Farquhar-type photosynthesis models. In all species, stomatal conductance increased exponentially with temperature over the whole range of 15 – 35 °C, even when A decreased at high measurement temperature. There were larger increases in conductance over this temperature range in the warm climate species (4.3 ×) than in the cool climate species (2.5 ×). The initial slope of A vs. C_i exhibited an optimum temperature which ranged from 20 to 30 °C. There was a larger increase in the optimum temperature of the initial slope at the warmer growth temperature in the cool climate species than in the warm climate species. The optimum temperature for A at high C_i ranged from 25 to 30 °C among species, but changed little with growth temperature. The absolute values of both the initial slope of A vs. C_i and A at high C_i were increased about 10% by growth at the warmer temperature in the warm climate species, and decreased about 20% in the cool climate species. The ratio of J_max — V_Cmax normalized to 20 °C varied by more than a factor of 2 across species and growth temperatures, but differences in the temperature response of photosynthesis were more related to variation in the temperature dependencies of J_max and V_Cmax than to the ratio of their normalized values.This revised version was published online in October 2005 with corrections to the Cover Date.     

Growth temperature can alter the temperature dependent stimulation of photosynthesis by elevated carbon dioxide in Albutilon theophrasti

Stimulation of photosynthesis in response to elevated carbon dioxide concentration [CO2] in the short-term (min) should be highly temperature dependent at high photon flux. However, it is unclear if long-term (days, weeks) adaptation to a given growth temperature alters the temperature-dependent stimulation of photosynthesis to [CO2]. In velveltleaf (Albutilon theophrasti), the response of photosynthesis, determined as CO2 assimilation, was measured over a range of internal CO2 concentrations at 7 short-term measurement (12, 16, 20, 24, 28, 32, 36 degrees C) temperatures for each of 4 long-term growth (16, 20, 28 and 32 degrees C) temperatures. In vivo estimates of VCmax, the maximum RuBP saturated rate of carboxylation, and Jmax, the light-saturated rate of potential electron transport, were determined from gas exchange measurements for each temperature combination. Overall, previous exposure to a given growth temperature adjusted the optimal temperatures of Jmax and VCmax with subsequently greater enhancement of photosynthesis at elevated [CO2] (i.e., a greater enhancement of photosynthesis at elevated [CO2] was observed at low measurement temperatures for A. theophrasti grown at low growth temperatures compared with higher growth temperatures, and vice versa for plants grown and measured at high temperatures). Previous biochemical based models used to predict the interaction between rising [CO2] and temperature on photosynthesis have generally assumed no growth temperature effect on carboxylation kinetics or no limitation by Jmax. In the current study, these models over predicted the temperature dependence of the photosynthetic response to elevated [CO2] at temperatures above 24 degrees C. If these models are modified to include long-term adjustments of Jmax and VCmax to growth temperature, then greater agreement between observed and predicted values was obtained.