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.     

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.     

C3 photosynthesis and high temperature acclimation of CAM in opuntia basilaris engelm. and bigel

Summary Carbon fixation by CAM at high night temperatures was examined in the stem succulent, Opuntia basilaris. Nighttime accumulation of titratable acids was uniformly high among plants growing naturally along an altitudinal temperature gradient in Death Valley, California during the hot summer period. Plants grown at high temperature regimes (40°/30°C) had rates of CAM and C₃ fixation similar to rates observed in plants maintained at a cool temperature (20°/10°C). C₃ fixation comprised 30% of the total carbon fixed by the potted, well watered plants. However, when pads were excised, C₃ fixation was suppressed while CAM continued unabated.     

Temperature responses of growth and photosynthetic CO2 exchange rates in coastal and desert races of Atriplex lentiformis

Summary Comparative measurements of CO₂ exchange and growth rates were made on Atriplex lentiformis (Torr.) Wats. plants from populations native to coastal as well as desert habitats in southern California. While both had similar CO₂ exchange rates at moderate growth temperatures, the desert plants had a substantially greater capacity to acclimate to high growth temperatures indicating that clear ecotypic differences in acclimation capacity are present in this species. This large capacity for photosynthetic acclimation resulted in nearly equal CO₂ exchange rates of the desert plants under the different day temperatures characteristic of the desert habitat during the summer and winter months. In contrast, the photosynthetic CO₂ exchange rates of the coastal plants was markedly reduced by high growth temperatures. The large acclimation capacity of the desert plants may function to maintain high productivities during both the winter and summer months but would not be required in the coastal plants because of the moderate temperatures throughout the year in their native habitat.Relative growth rates (RGR) of the coastal and desert plants were similar at 23°C day/18°C night and 33°C day/25°C night growth temperatures. At 43°C day/30°C night temperatures, however, the RGR of the desert plants was higher than that of the coastal plants. Thus, the larger acclimation capacity of the desert plants is related to a greater ability to maintain high growth rates over a wide range of temperatures as compared to the coastal plants. Small differences in allocation patterns could account for differences in the comparative photosynthetic responses and growth rates in each temperature regime.Supported by National Science Foundation grant # GB 36311     

C4 photosynthesis in Spartina townsendii at low and high temperatures

The metabolism of ¹⁴CO₂ in the cool temperate saltmarsh grass Spartina townsendii was investigated in plants grown in their natural habitats at two temperatures. Both in the spring at 10°C and in the late summer at 25°C radioactivity was initially incorporated into the organic acids malate and aspartate and then transferred to 3-phosphoglycerate in the manner characteristic of the C₄ pathway of photosynthesis. Metabolism was not disrupted at the lower temperature as in some C₄ plants. Radioactivity was transferred more slowly from malate into alanine, glycine and serine at 10°C, but sugars were labelled equally at both temperatures.     

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.     

PHOTOSYNTHETIC SENSITIVITY TO TEMPERATURE IN POPULATIONS OF TWO C4 BOUTELOUA (POACEAE) SPECIES NATIVE TO DIFFERENT ALTITUDES

The relationships between photosynthesis, flowering, and growth temperatures were examined experimentally in four populations of the C₄ grass genus Bouteloua. Field-collected plants were grown under two temperature regimes, cool (20 C day/6 C night) and warm (30/16), representative of the extreme populations. Populations collected from the warm climates had significantly lower photosynthetic capacity when grown in the cool chamber relative to the warm chamber, while photosynthetic capacity in the cool climate populations did not differ between the growth conditions. Additionally, exposure to a 2-day cold temperature treatment (10/-2), representative of late-season frosts in high altitude sites, resulted in further reductions in photosynthesis in the warm climate plants, but not in the cool climate plants. This effect was greater for plants grown in the cool growth chamber. Flowering was reduced by 70% in the warm climate plants grown in the cool chamber, and was correlated with photosynthetic inhibition following the short-term cold temperature treatment. These results indicate that genetic differentiation for photosynthetic temperature sensitivity has occurred in the cool climate populations, and that long-term exposure to cool temperatures coupled with short-term relatively extreme low temperatures results in greater photosynthetic inhibition in nontolerant populations.     

Photosynthetic responses of C3 and C4 species from cool shaded habitats in Hawaii

Summary The C₄ species, Euphorbia forbesii, and the C₃ species, Claoxylon sandwicense, occupy cool, shaded habitats in Hawaii. Both of these species exhibit the photosynthetic characteristics of typical shade plants: low light-saturated photosynthetic rates, low dark respiration rates, low light levels for saturation of photosynthesis, and low light compensation points. In addition, the quantum yields of the two species are similar at leaf temperatures near 22°C, reflecting a significant increase in the quantum yield of E. forbesii over that of C₄ species from open habitats. C. sandwicense has a lower dark respiration rate than E. forbesii. Hence, since the quantum yields of the two species are similar at cool temperatures, C. sandwicense has a higher photosynthetic rate than E. forbesii at low incident photon flux densities. As a consequence, C. sandwicense should have a greater carbon gain than E. forbesii under the diffuse radiation conditions of their native habitat. However, since E. forbesii has a higher light-saturated photosynthetic rate than C. sandwicense, E. forbesii may have a greater carbon gain than C. sandwicense during sunflecks.     

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.     

Temperature and water regulation of gas exchange of Opuntia polyacantha

Summary Opuntia polyacantha was collected from the shortgrass prairie in Colorado. Carbon dioxide and water vapor exchange was monitored in plants pretreated and analyzed under cool temperatures (20/15°C) and warm temperatures (35/15°C). Well watered plants under a 35/15 thermoperiod supported the fixation of atmospheric CO₂ during the night, early morning, and late afternoon. Plants under a 20/15 thermoperiod exhibited CO₂ uptake only during the afternoon. The fixation of CO₂ at night could be stimulated or induced by decreasing the night temperature. Plants from which water was withheld two or four weeks showed a decline in CO₂ fixation with the uptake at night exhibiting the greatest sensitivity. Under conditions of water stress the enhancement of CO₂ uptake at night by cool night temperatures was largely lost. Plants water stressed for 4 weeks recovered rapidly upon rewatering under warm or cool temperatures. Rates of CO₂ fixation were comparable to well watered plants within 24 h. The effects of temperature and water stress on gas exchange are compared to the in situ growth pattern of O. polyacantha and contrasted with the regulation of gas exchange observed in C₃ and C₄ grasses of the shortgrass prairie.This research was supported by funds from NSF Grants BMS 74-07894, GB-31862X, and GB-41233X     

Orientation and its consequences for Copiapoa (Cactaceae) in the Atacama Desert

Summary Three species of the barrel cactus Copiapoa (C. cinerea, C. columna-alba, C. haseltoniana) were investigated in their native habitats along the cool, arid coastal regions of the Atacama Desert in northern Chile. All species orient towards the north with a high degree of precision. Two consequences of adaptive value result from this northerly orientation. First, tissue temperatures of the meristematic and floral regions on the tip of the cactus receive high solar radiation loads which result in high temperatures (30°–40°C) relative to air temperatures (15°–20°) during winter and spring months when adequate soil moisture for growth is available. Second, absorption of solar radiation by the sides of the cactus is minimized, which reduces both the potential detrimental effects of light and heat load on the cactus and probably balances daily quanta absorbed for photosynthesis with nighttime CO₂ uptake rates during drought stress periods.     

Leaf hairs: Effects on physiological activity and adaptive value to a desert shrub

Summary The effects of leaf hairs on photosynthesis, transpiration, and leaf energy balance were measured on the desert shrub Encelia farinosa in order to determine the adaptive significance of the hairs. The pubescence reduces leaf absorptance resulting in a reduced heat load, and as a consequence lower leaf temperatures and lower transpiration rates. In its native habitat where air temperatures often exceed 40° C, the optimum temperature for photosynthesis in E. farinosa occurs at 25° C, and at leaf temperatures above 35° C net photosynthesis declines precipitously. An advantage of leaf pubescence is that it allows a leaf temperature much lower than air temperature. As a result, leaf temperatures are near the temperature optimum for photosynthesis and high, potentially lethal leaf temperatures are avoided. However, there is a disadvantage associated with leaf pubescence. By reflecting quanta that might otherwise be used in photosynthesis, the presence of leaf hairs reduces the rate of photosynthesis. A tradeoff model was used to assess the overall advantage of possessing leaf hairs. In terms of the carbon gaining capacity of the leaf, the model predicted that for different environmental conditions different levels of leaf pubescence were optimal. In other words, under aird conditions and/or high air temperatures, leaves of E. farinosa would have a higher rate of photosynthesis by being pubescent than by not being pubescent. The predictions from this model agreed closely with observed patterns of leaf pubescence in the field.C.I.W.-D.P.B. Publication No. 613     

Temperature and salinity regulation of growth and gas exchange of Salicornia fruticosa (L.) L.

Summary Salicornia fruticosa was collected from a salt marsh on the Mediterranean sea coast in Libya. Growth and gas exchange of this C₃ species were monitered in plants pretreated at various NaCl concentrations (0, 171, 342, 513 and 855 mM). Maximum growth was at 171 mM NaCl under cool growth conditions (20/10° C) and at 342 mM NaCl under warm growth conditions (30/15° C) with minimum growth at 0 mM NaCl (control). Net photosynthesis (Pn) was greatest in plants grown in 171 mM NaCl with plants grown at 513 and 855 mM having lowest rates. Maximum Pn was at 20–25° C shoot temperatures with statistically significant reductions at 30° C in control plants while salt treated plants showed such reductions at 35° C. Salt treatments increased dark respiration over the control at 171 and 342 mM but reduced it at higher concentrations. Photorespiration was reduced by salt treatment and increased by increasing shoot temperature. Greatest transpiration was in 171 mM NaCl treated plants and increasing shoot temperature increased transpiration in all treatments. Stomatal resistance to CO₂ influx was influenced only moderately by temperature while increasing salinity resulted in increased stomatal resistance. In general both temperature and salinity increased the mesophyll resistance to CO₂ influx. The species seems adapted to the warm saline habitat along the Mediterranean sea coast, at least partially, by its ability to maintain relatively high Pn at moderate NaCl concentrations over a broad range of shoot temperatures.     

Carbon dioxide exchange in Cladina lichens from subarctic and temperate habitats

Summary The survival potential of lichens in a given habitat is determined by the response of CO₂ exchange to photosynthetically active radiation (PhAR), thallus temperature, and thallus relative water content (RWC). Therefore morphologically similar lichens from contrasting climatic environments 1) should differ in their CO₂ exchange responses, and 2) these differences should reflect adaptations to their climatic regimes. The CO₂ exchange responses of a subarctic (55°N, 67°W) Cladina stellaris (Opiz) Brodo population and a temperate (29°N, 82°W) Cladina evansii (Abb.) Hale and W. Culb, population were used to test these two related hypotheses.Infrared gas analysis with lichens collected in September–October 1975 established that the two populations differed in their responses to incident PhAR, thallus temperature, and thallus RWC. Net photosynthesis in C. stellaris had an optimum at a lower temperature and a greater relative photosynthetic capacity at low temperatures than did C. evansii. Cladina evansii maintained net photosynthesis above 35°C thallus temperature; C. stellaris did not. In both species the optimum temperature for net photosynthesis increased with increasing irradiance. The C. stellaris light saturation point was consistently lower than that of C. evansii. Both species had maximal rates of net photosynthesis at 70–80% relative water content. In C. evansii the CO₂ exchange rates, expressed as percentages of the maximum rate, declined more rapidly under suboptimal conditions. The absolute CO₂ exchange rates of C. evansii were greater than those of C. stellaris. At 20°C and 90–95% RWC, resaturation respiration occurred in both species and continued until 6–7 h after wetting.Contrasts in the temporal patterns of thallus condition at each collection site suggest that not all differences in the two response surfaces reflect climatic adaptation. The two populations appear well adapted to incident PhAR and thallus temperature regimes but the 70–80% RWC optimum for net photosynthesis common to both species is puzzling since their water regimes differ markedly. The overall adaptedness of the CO₂ exchange responses in the two species cannot be judged without a comprehensive quantitative analysis of carbon balance under differing climatic regimes.     

Photosynthetic 14CO2 fixation products in altitudinal ecotypes of Trifolium repens L. with different temperature requirements

Summary Two Trifolium repens clones from natural meadows at 600 m and 2030 m above sea level, and with differing dependence on temperature of their rate of apparent photosynthesis, were grown under controlled environments. Radioactive products in detached leaves were examined after 20 and 40 s periods of steady state photosynthesis in ¹⁴CO₂ at 3° C and 24° C. Glycine and serine were hardly labeled at 3° C. At 24° C, the leaves of the alpine clone showed significantly, (P<0.025) more activity in these amino acids than those from the low altitude clone. It is suggested that the alpine clone has a higher photorespiration. This is supported by the labeling pattern of glucose, fructose, sucrose, and glucose-6-phosphate.The high altitude clone requires lower temperatures for photosynthesis than the low altitude clone. It is suggested, that this is caused by its higher photorespiration, which reduces net photosynthesis at high temperatures. The lower photorespiration activity of the low altitude clone can be interpreted as an adaptation to its warmer habitat.     

The subdominant status of Echinocereus viridiflorus and Mammillaria vivipara in the shortgrass prairie: The role of temperature and water effects on gas exchange

Summary The subdominant CAM species, Echinocereus viridiflorus and Mammillaria vivipara, collected from the shortgrass prairie in northeastern Colorado were pretreated and analyzed for gas exchange under cool temperatures (20/15°C) and warm temperatures (35/15°C). Well watered plants of both species under a 35/15°C thermoperiod fixed atmospheric CO₂ during the night and early moring. Echinocereus viridiflorus grown and analyzed at 20/15°C fixed CO₂ during the night, early morning and late afternoon but total carbon gain over a 24 h period is less than when grown and analyzed under the 35/15°C thermoperiod. Mammillaria vivipara grown and analyzed at 20/15°C assimilates CO₂ at low rates during all parts of a 24 h period with the greatest CO₂ fixation rates occuring from midday to late afternoon. The total carbon gain under the 20/15°C thermoperiod is less than that for this species under the 35/15°C thermoperiod. Decreasing the night temperature of plants grown under the warm conditions to 10°C or 5°C results in a depression of the night CO₂ fixation in both species. E. viridiflorus from the cool growth conditions showed an enhancement of the CO₂ uptake during the night, early morning and late afternoon when subjected to the cooler night temperatures (10°C and 5°C). The CO₂ uptake of M. vivipara grown at 20/15°C shows an enhancement during the night and early morning while the CO₂ fixation during midday and late afternoon is slightly depressed under cool night temperatures (10° and 5°C). Under the 35/15°C thermoperiod both species exhibit depressed rates of CO₂ fixation during the night and early morning when water stressed. Plants of both species grown under the 20/15°C thermoperiod exhibit no net CO₂ fixation following five weeks of water deprivation. Upon rewatering, E. viridiflorus begins to recover its capacity for CO₂ fixation within 24 h under both the warm and cool temperature regimes. However, M. vivipara did not show recovery within 48 h following rewatering under the warm or cool temperature regime. Contrasting the patterns of gas exchange of the subdominant species, E. viridiflorus and M. vivipara, with a dominant CAM species of the shortgrass prairie, Opuntia polyacantha reveals significant differences that may well dictate the role of these species in this ecosystem. E. viridiflorus and M. vivipara have a lower capacity of carbon gain and recovery from water stress than O. polyacantha mainly due to their lack of late afternoon CO₂ uptake. This study suggests that carbon gain plays an important role in limiting E. viridiflorus and M. vivipara in the shortgrass prairie ecosystem.     

Dependence of CO2 gas exchange and acid metabolism of the alpine CAM plant Sempervivum montanum on temperature and light

Summary The influence of light intensity and temperature on the diurnal course and magnitude of CO₂ gas exchange and on acid metabolism was studied in the laboratory with rooted rosettes of Sempervivum montanum collected at 2,200 m above sea level in the Central Alps. Under a temperature regime having a cool dark period and warm light period, S. montanum exhibited the time course of CO₂ gas exchange typical of a CAM plant; the response was very distinct even when the plants were well-watered. At day temperatures of less than 10° C and at night temperatures greater than 35° C, S. montanum behaved like a C₃ plant. Characteristic for S. montanum are a broad temperature optimum and a wide range of temperatures in which CO₂ uptake in light is possible (-2° to 45° C). Dark fixation of CO₂ is evident between-2° and 35° C, an apparent uptake of external CO₂, on the other hand, only as high as 20° C. Light saturation of CO₂ uptake is reached at 60–80 W m^-2 while the rate of deacidification is nearly maximal at 40 W m^-2. These results show that, due to their specific metabolism, CAM plants can be favored not only in xeric habitats, but also in heat stressed mountain habitats where the daily variation in temperature may be extreme.Dedicated with appreciation to Dr. K.F. Springer     

Physiological studies of subtidal red algae

The net photosynthesis of the subtidal red algae Euthora cristata (C. Agardh) J. Agardh, Phycodrys rubens (L. ) Batters, Phyllophora truncata (Pallas) Newroth et Taylor and Ptilota serrata Kützing were determined under a variety of different light and temperature regimes. The optimal light requirements for net photosynthesis of the species are relatively low, mostly ranging from 465 to 747 ft-c at 5 ° and 15 °C. Seasonal and spatial differences were found in the photosynthesis-light responses of Phyllophora truncata and Ptilota serrata; winter plants exhibited lower light optima for net photosynthesis than spring plants. Deep-water populations of Ptilota showed lower light optima and reduced net photosynthesis as compared with shallow subtidal populations. Summer plants of Euthora cristata, Phycodrys rubens and Phyllophora truncata showed a greater tolerance to high temperatures and higher temperature optima than winter plants. It is suggested that optimal temperature and light requirements of seaweeds are adjusted in an adaptive fashion to the environmental regimes of their habitats. The temperature requirements of the four species are discussed in relation to their local estuarine distributions in New England; eurythermal species have the widest estuarine distributions. Cystocarpic and tetrasporic plants of Euthora cristata and Ptilota serrata show differential physiological responses and vertical distributions. The significance of higher rates of net photosynthesis and lower light optima are discussed in relation to vertical stratification of different generations.     

Subtle topographical differences along a floodplain promote different plant strategies among Paspalum dilatatum subspecies and populations

It was hypothesised that subtle topographical differences might cause the existence of ecotypes along a floodplain. The apomict grass Paspalum dilatatum subspecies dilatatum inhabits flood‐prone lowlands as well as nearby uplands in the floodplains of Argentina, while the sexual P. dilatatum subspecies flavescens almost exclusively inhabits the uplands. The aim of the present study was to identify the different traits that allow these P. dilatatum populations to inhabit different habitats. Plants of P. dilatatum were reciprocally transplanted between uplands and lowlands. Morphophysiological traits related to flooding tolerance were measured during a flood. Subspecies dilatatum from the uplands and subspecies flavescens showed a high physiological performance in the uplands but a considerable decrease in stomatal conductance, net photosynthesis rates and tiller number in the flooded lowlands. In contrast, the subspecies dilatatum from the lowlands showed relatively lower and stable stomatal conductance, photosynthesis rates and leaf water potential at both sites. Subspecies dilatatum from the lowlands outperformed upland populations at the lowland site with respect to tillering. Leaves of subspecies dilatatum from the lowlands that had grown at the lowland habitat had a lower blade/sheath proportion than leaves of plants transplanted to the uplands. This behavior did not occur in both upland populations. Results suggest that dilatatum Lowland plants have the typical strategy of stress‐tolerant genotypes and that the upland populations are adapted to habitats where competitive species are selected. In conclusion, habitats with subtle differences in topographic level can favour both ecotypic differentiations within an apomict subspecies but also the maintenance of morphophysiological similitudes between coexisting upland populations belonging to different subspecies.     

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.