Seasonal patterns of photosynthetic response and acclimation to elevated carbon dioxide in field-grown strawberry

Strawberry (Fragaria × ananassa) plants were grown in field plots at the current ambient [CO₂], and at ambient + 300 and ambient + 600 μmol mol⁻¹ [CO₂]. Approximately weekly measurements were made of single leaf gas exchange of upper canopy leaves from early spring through fall of two years, in order to determine the temperature dependence of the stimulation of photosynthesis by elevated [CO₂], whether growth at elevated [CO₂] resulted in acclimation of photosynthesis, and whether any photosynthetic acclimation was reduced when fruiting created additional demand for the products of photosynthesis. Stimulation of photosynthetic CO₂ assimilation by short-term increases in [CO₂] increased strongly with measurement temperature. The stimulation exceeded that predicted from the kinetic characteristics of ribulose-1,5-bisphosphate carboxylase at all temperatures. Acclimation of photosynthesis to growth at elevated [CO₂] was evident from early spring through summer, including the fruiting period in early summer, with lower rates under standard measurement conditions in plants grown at elevated [CO₂]. The degree of acclimation increased with growth [CO₂]. However, there were no significant differences between [CO₂] treatments in total nitrogen per leaf area, and photosynthetic acclimation was reversed one day after switching the [CO₂] treatments. Tests showed that acclimation did not result from a limitation of photosynthesis by triose phosphate utilization rate at elevated [CO₂]. Photosynthetic acclimation was not evident during dry periods in midsummer, when the elevated [CO₂] treatments conserved soil water and photosynthesis declined more at ambient than at elevated [CO₂]. Acclimation was also not evident during the fall, when plants were vegetative, despite wet conditions and continued higher leaf starch content at elevated [CO₂]. Stomatal conductance responded little to short-term changes in [CO₂] except during drought, and changed in parallel with photosynthetic acclimation through the seasons in response to the long-term [CO₂] treatments. The data do not support the hypothesis that source-sink balance controls the seasonal occurrence of photosynthetic acclimation to elevated [CO₂] in this species. This revised version was published online in June 2006 with corrections to the Cover Date.     

Response of Photosynthetic Apparatus of Spring Barley (Hordeum vulgare L.) to Combined Effect of Elevated CO2 Concentration and Different Growth Irradiance

The response of barley (Hordeum vulgare L. cv. Akcent) to various photosynthetic photon flux densities (PPFDs) and elevated [CO₂] [700 μmol (CO₂) mol⁻¹; EC] was studied by gas exchange, chlorophyll (Chl) a fluorescence, and pigment analysis. In comparison with barley grown under ambient [CO₂] [350 μmol (CO₂) mol⁻¹; AC] the EC acclimation resulted in a decrease in photosynthetic capacity, reduced stomatal conductance, and decreased total Chl content. The extent of acclimation depression of photosynthesis, the most pronounced for the plants grown at 730 μmol m⁻² s⁻¹ (PPFD₇₃₀), may be related to the degree of sink-limitation. The increased non-radiative dissipation of absorbed photon energy for all EC plants corresponded to the higher de-epoxidation state of xanthophylls only for PPFD₇₃₀ barley. Further, a pronounced decrease in photosystem 2 (PS2) photochemical efficiency (given as F_V/F_M) for EC plants grown at 730 and 1 200 μmol m⁻² s⁻¹ in comparison with AC barley was related to the reduced epoxidation of antheraxanthin and zeaxanthin back to violaxanthin in darkness. Thus the EC conditions sensitise the photosynthetic apparatus of high-irradiance acclimated barley plants (particularly PPFD₇₃₀) to the photoinactivation of PS2. This revised version was published online in August 2006 with corrections to the Cover Date.     

Stomatal acclimation to increased CO2 concentration in a Florida scrub oak species Quercus myrtifolia Willd

Native scrub‐oak communities in Florida were exposed for three seasons in open top chambers to present atmospheric [CO₂] (approx. 350 μmol mol^?1) and to high [CO₂] (increased by 350 μmol mol^?1). Stomatal and photosynthetic acclimation to high [CO₂] of the dominant species Quercus myrtifolia was examined by leaf gas exchange of excised shoots. Stomatal conductance (g_s) was approximately 40% lower in the high‐ compared to low‐[CO₂]‐grown plants when measured at their respective growth concentrations. Reciprocal measurements of g_s in both high‐ and low‐[CO₂]‐grown plants showed that there was negative acclimation in the high‐[CO₂]‐grown plants (9–16% reduction in g_s when measured at 700 μmol mol^?1), but these were small compared to those for net CO₂ assimilation rate (A, 21–36%). Stomatal acclimation was more clearly evident in the curve of stomatal response to intercellular [CO₂] (c_i) which showed a reduction in stomatal sensitivity at low c_i in the high‐[CO₂]‐grown plants. Stomatal density showed no change in response to growth in high growth [CO₂]. Long‐term stomatal and photosynthetic acclimation to growth in high [CO₂] did not markedly change the 2·5‐ to 3‐fold increase in gas‐exchange‐derived water use efficiency caused by high [CO₂].     

Consequences of growth at two carbon dioxide concentrations and two temperatures for leaf gas exchange in Pascopyrum smithii (C3) and Bouteloua gracilis (C4)*

Continually rising atmospheric CO₂ concentrations and possible climatic change may cause significant changes in plant communities. This study was undertaken to investigate gas exchange in two important grass species of the short-grass steppe, Pascopyrum smithii (western wheat-grass), C₃, and Bouteloua gracilis (blue grama), C4, grown at different CO₂ concentrations and temperatures. Intact soil cores containing each species were extracted from grasslands in north-eastern Colorado, USA, placed in growth chambers, and grown at combinations of two CO₂ concentrations (350 and 700 μmol mol⁻¹) and two temperature regimes (field average and elevated by 4°C). Leaf gas exchange was measured during the second, third and fourth growth seasons. All plants exhibited higher leaf CO₂ assimilation rates (A) with increasing measurement CO₂ concentration, with greater responses being observed in the cool-season C₃ species P. smithii. Changes in the shape of intercellular CO₂ response curves of A for both species indicated photosynthetic acclimation to the different growth environments. The photosynthetic capacity of P. smithii leaves tended to be reduced in plants grown at high CO₂ concentrations, although A for plants grown and measured at 700μmol mol⁻¹ CO₂ was 41% greater than that in plants grown and measured at 350 μmol mol⁻¹ CO₂. Low leaf N concentration may have contributed to photosynthetic acclimation to CO₂. A severe reduction in photosynthetic capacity was exhibited in P. smithii plants grown long-term at elevated temperatures. As a result, the potential response of photosynthesis to CO₂ enrichment was reduced in P. smithii plants grown long-term at the higher temperature.     

Effects of elevated CO<Subscript>2</Subscript> and nitrogen on wheat growth and photosynthesis

The effects of nitrogen [75 and 150 kg (N) ha⁻¹] and elevated CO₂ on growth, photosynthetic rate, contents of soluble leaf proteins and activities of ribulose-1,5-bisphosphate carboxylase/oxygenase (Rubisco) and nitrate reductase (NR) were studied on wheat (Triticum aestivum L. cv. HD-2285) grown in open top chambers under either ambient (AC) or elevated (EC) CO₂ concentration (350 ± 50, 600 ± 50 μmol mol⁻¹) and analyzed at 40, 60 and 90 d after sowing. Plants grown under EC showed greater photosynthetic rate and were taller and attained greater leaf area along with higher total plant dry mass at all growth stages than those grown under AC. Total soluble and Rubisco protein contents decreased under EC but the activation of Rubisco was higher at EC with higher N supply. Nitrogen increased the NR activity whereas EC reduced it. Thus, EC causes increased growth and P_N ability per unit uptake of N in wheat plants, even if N is limiting.     

Photosynthetic acclimation to CO2 enrichment related to ribulose-1,5-bisphosphate carboxylation limitation in wheat

Net photosynthetic rate (P _N) measured at the same CO₂ concentration, the maximum in vivo carboxylation rate, and contents of ribulose-1,5-bisphosphate (RuBP) carboxylase/oxygenase (RuBPCO) and RuBPCO activase were significantly decreased, but the maximum in vivo electron transport rate and RuBP content had no significant change in CO₂-enriched [EC, about 200 μmol mol⁻¹ above the ambient CO₂ concentration (AC)] wheat leaves compared with those in AC grown wheat leaves. Hence photosynthetic acclimation in wheat leaves to EC is largely due to RuBP carboxylation limitation.     

Modelling Net Photosynthetic Rate of Winter Wheat in Elevated Air CO2 Concentrations

Winter wheat plants were grown in open top chambers either at 365 µmol mol^–1 (AC) or at 700 µmol mol^–1 (EC) air CO₂ concentrations. The photosynthetic response of flag leaves at the beginning of flowering and on four vertical leaf levels at the beginning of grain filling were measured. Net photosynthetic rates (P _N) were higher at both developmental phases in plants grown at EC coupled with larger leaf area and photosynthetic pigment contents. The widely accepted Farquhar net photosynthesis model was parameterised and tested using several observed data. After parameterisation the test results corresponded satisfactorily with observed values under several environmental conditions.     

Photosynthetic characteristics of Amaranthus tricolor,a C4 tropical leafy vegetable

The gas exchange characteristics are reported for Amaranthus tricolor, a C₄ vegetable amaranth of southeastern Asia. Maximum photosynthetic capacity was 48.3±1.0μmol CO₂ m^?2s^?1 and the temperature optimum was 35°C. The calculated intercellular CO₂ concentration at this leaf temperature and an incident photon flux (400–700 mm) of 2 mmol m^?2s^?1 averaged 208±14 μl l^?1, abnormally high for a C₄ species. The photosynthetic rate, intercellular CO₂ concentration, and leaf conductance all decreased with an increase in water vapor pressure deficit. However, the decrease in leaf conductance which resulted in a decrease in intercellular CO₂ concentration accounted for only one fourth of the observed decrease in photosynthetic rate as water vapor pressure deficit was increased. Subsequent measurements indicated that the depence of net photosynthesis on intercellular CO₂ concetration changed with water vapor pressure deficit.     

Photosynthetic characteristics of Amaranthus tricolor,a C4 tropical leafy vegetable

The gas exchange characteristics are reported for Amaranthus tricolor, a C₄ vegetable amaranth of southeastern Asia. Maximum photosynthetic capacity was 48.3±1.0 μmol CO₂ m^-2 s^-1 and the temperature optimum was 35°C. The calculated intercellular CO₂ concentration at this leaf temperature and an incident photon flux (400–700 mm) of 2 mmol m^-2 s^-1 averaged 208±14 μl l^-1, abnormally high for a C₄ species. The photosynthetic rate, intercellular CO₂ concentration, and leaf conductance all decreased with an increase in water vapor pressure deficit. However, the decrease in leaf conductance which resulted in a decrease in intercellular CO₂ concentration accounted for only one fourth of the observed decrease in photosynthetic rate as water vapor pressure deficit was increased. Subsequent measurements indicated that the dependence of net photosynthesis on intercellular CO₂ concentration changed with water vapor pressure deficit.     

Response of nodulated alfalfa to water supply,temperature and elevated CO2: productivity and water relations

Exposing plants to long-term CO₂ enrichment generally leads to increases in plant biomass, total leaf area and alterations on leaf net photosynthetic rates, stomatal conductance and water use efficiency. However, the magnitude of such effects is dependent on the availability of other potentially limiting resources. The aim of our study was to elucidate the effects of elevated CO₂, applied at different temperature and water availability regimes, on nodulated alfalfa plants. Regardless of water supply, elevated CO₂ enhanced plant growth, especially when combined with increased temperature although no differences were detected until 30 days of treatment. Absence of differences in leaf relative growth rate, and gas exchange measurements, suggested that plants grown in a low water regime adjusted their growth to the amount of available water. Elevated CO₂ enhanced water use efficiency because of reduced water consumption and a greater dry mass production. Increased dry matter production of plants grown under elevated CO₂ and temperature was the result of stimulated photosynthetic rates, greater leaf area and water use efficiency. Lack of CO₂ effect on photosynthesis of plants grown at ambient temperature might be consequence of down-regulation phenomena. Plants grown at 700 μmol mol⁻¹ CO₂ maintained control nitrogen levels, discarding enhanced nitrogen availability as the main factor explaining enhanced dry matter.     

Soybean leaf growth and gas exchange response to drought under carbon dioxide enrichment

This study was conducted to determine the response in leaf growth and gas exchange of soybean (Glycine max Merr.) to the combined effects of water deficits and carbon dioxide (CO₂) enrichment. Plants grown in pots were allowed to develop initially in a glasshouse under ambient CO₂ and well-watered conditions. Four-week old plants were transferred into two different glasshouses with either ambient (360 μmol mol^-1) or elevated (700 μmol mol^-1) CO₂. Following a 2-day acclimation period, the soil of the drought-stressed pots was allowed to dry slowly over a 2-week period. The stressed pots were watered daily so that the soil dried at an equivalent rate under the two CO₂ levels. Elevated [CO₂] decreased water loss rate and increased leaf area development and photosynthetic rate under both well-watered and drought-stressed conditions. There was, however, no significant effect of [CO₂] in the response relative to soil water content of normalized leaf gas exchange and leaf area. The drought response based on soil water content for transpiration, leaf area, and photosynthesis provide an effective method for describing the responses of soybean physiological processes to the available soil water, independent of [CO₂].     

Influence of Etherel and Gibberellic Acid on Carbon Metabolism,Growth, and Essential Oil Accumulation in Spearmint (Mentha Spicata)

Controlled environment chamber and glasshouse studies were conducted on six herbaceous annual species grown at 350 (AC) and 700 (EC) mol(CO₂) mol^-1 to determine whether growth at EC resulted in acclimation of the apparent quantum yield of photosynthesis (QY) measured at limiting photosynthetic photon flux density (PPFD), or in acclimation of net photosynthetic rate (P _N) measured at saturating PPFD. It was also determined whether acclimation in P _N at limiting PPFD was correlated with acclimation of carboxylation efficiency or ribulose-1,5-bisphosphate (RuBP) regeneration rate measured at saturating PPFD. Growth at EC reduced both the QY and P _N at limiting PPFD in three of the six species. The occurrence of photosynthetic acclimation measured at a rate limiting PPFD was independent of whether photosynthetic acclimation was apparent at saturating measurement PPFD. At saturating measurement PPFD, acclimation to EC in the apparent carboxylation efficiency and RuBP regeneration capacity also occurred independently. Thus at least three components of the photosynthetic system may adjust independently when leaves are grown at EC. Estimates of photosynthetic acclimation at both high and low PPFD are necessary to accurately predict photosynthesis at the whole plant or canopy level as [CO₂] increases.     

The Effects of N Nutrition on the Water Relations and Gas Exchange Characteristics of Wheat (Triticum aestivum L.)

The purpose of this study was to characterize leaf photosynthetic and stomatal responses of wheat (Triticum aestivum L.) plants grown under two N-nutritional regimes. High- and low-N regimes were imposed on growth-chamber-grown plants by fertilizing with nutrient solutions containing 12 or 1 millimolar nitrogen, respectively. Gas-exchange measurements indicated not only greater photosynthetic capacity of high-N plants under well-watered conditions, but also a greater sensitivity of CO₂ exchange rate and leaf conductance to CO₂ and leaf water potential compared to low-N plants. Increased sensitivity of high-N plants was associated with greater tissue elasticity, lower values of leaf osmotic pressure and greater aboveground biomass. These N-nutritional-related changes resulted in greater desiccation (lowered relative water content) of high-N plants as leaf water potential fell, and were implicated as being important in causing greater sensitivity of high-N leaf gas exchange to reductions in water potential. Water use efficiency of leaves, calculated as CO₂ exchange rate/transpiration, increased from 9.1 to 13 millimoles per mole and 7.9 to 9.1 millimoles per mole for high- and low-N plants as water became limiting. Stomatal oscillations were commonly observed in the low-N treatment at low leaf water potentials and ambient CO₂ concentrations, but disappeared as CO₂ was lowered and stomata opened.     

Effect of dehydration and high light on photosynthesis of two C3 plants (Phaseolus vulgaris L. and Elatostema repens (Lour.) Hall f.)

The effect of drought on the photosynthetic functioning of two C₃ plants, Phaseolus vulgaris and Elatostema repens, has been examined. Leaf net CO₂ uptake measured in normal air was negligible at a leaf water deficit of about 30% while the calculated leaf intercellular CO₂ concentration (Ci) was unchanged. However, both the maximal photosynthetic capacity (CO₂-dependent O₂ evolution) and apparent quantum yield, measured in the presence of saturating CO₂ levels (5 to 14%), only started to decrease within the range of 25 to 30% leaf water deficit. This shows that the drought-induced inhibition seen in normal air is not caused by an inhibition of the photosynthetic mechanism, and that in this case Ci values can be misleading. Both 77 K and room-temperature fluorescence measurements indicate that the functioning of the photosystem-II reaction centre is hardly modified by water shortage. Furthermore, an analysis of photochemical chlorophyll fluorescence quenching shows, in the absence of CO₂, that O₂ can be an efficient acceptor of photosynthetic energy, even in severly dehydrated plants which do not show net CO₂ uptake in normal air. In these plants, O₂ is probably reduced mainly via Mehler-type reactions. High-light treatment given at low O₂ increases photoinhibition as measured by the decrease of apparent quantum yield in dehydrated P. vulgaris, whereas, interestingly, 1% O₂ protects dehydrated E. repens against high-light damage. The two plants could have different protective mechanisms depending upon the O₂ level or different photoinhibitory sites or mechanisms.Abbreviations and symbols Ca, Ci ambient and calculated intercellular CO₂ concentration - Fm, Fo, Fv maximum, initial and variable fluorescence emission - LWD leaf water deficit - PPFD photosynthetic photon flux density - PSII photosystem II - qQ photochemical quenching of chlorophyll fluorescence     

Whole-plant gas exchange responses of Spartina alterniflora (Poaceae) to a range of constant and transient salinities

A two-chamber-system was used to study whole-plant gas exchange responses of Spartina alterniflora to long-term and transient salinity treatments over the range of 5 to 40 ppt NaCl. Lower photosynthetic rates, leaf water vapor conductances, belowground respiration rates, and higher aboveground respiration rates in plants adapted to 40 ppt NaCl were observed. Area-specific leaf weight increased with salinity, although the salt content of leaf tissues did not. A reduced rate of gross photosynthesis and higher aboveground respiration rate in 40-ppt NaCl plants significantly lowered the net whole-plant CO₂ gain below that of 5-ppt NaCl plants, while the net CO₂ gain of 25-ppt NaCl plants was intermediate. Within 6 hr of increasing the salinity of 5- and 25-ppt NaCl plants by 20 and 15 ppt NaCl, S. alterniflora responded by reducing leaf water vapor conductance, which in turn reduced the photosynthetic rate. This response was reversed by returning the plants to their original salinity, which indicates that S. alterniflora adjusts water loss and gas exchange in response to transient salinity stress by regulating stomatal aperture. On the other hand, decreasing salinity of the growth media of plants cultured at 25 and 40 ppt NaCl had little or no effect on gas exchange characteristics. This suggests that S. alterniflora adapts to constant salinity through fixed, salinity-dependent structural modifications, such as stomatal density.     

Photosynthesis in Plants of Four Tropical Species Growing under Elevated CO2

We studied the responses of leaf gas exchange and growth to an increase in atmospheric CO₂ concentration in four tropical deciduous species differing in carbon fixation metabolism: Alternanthera crucis, C3-C4; Ipomoea carnea, C3; Jatropha gossypifolia, C3; and Talinum triangulare, inducible-CAM. In the first stage, plants were grown in one open-top chamber at a CO₂ concentration of 560±40 mol mol^-1 (EC), one ambient CO₂ concentration chamber (AC), and one unenclosed plot (U). In the second stage, plants were grown in five EC chambers (CO₂ concentration = 680±30 mol mol^-1), five AC chambers, and five unenclosed plots. During the first weeks under EC in the first stage, plants of all the species had a very marked increase in their maximal net photosynthetic rates (P _max) of 3.5 times on average; this stimulatory effect was maintained for 11-15 weeks, rates dampening afterward to values still higher than controls for 37 weeks. After a suspension of CO₂ enrichment for 6 weeks, an increase in P _max of EC plants over the controls was found in plants of all the species until week 82 of the experiment. Stomatal conductance (g) showed no response to EC. Carboxylation efficiency decreased in all the species under EC     

Influence of Drought,Rain and Artificial Irrigation on Photosynthesis,Gas Exchange and Water Relations of the Fynbos Plant Protea acaulos (L.) Reich at the End of the Dry Season

Protea acaulos, a prostrate fynbos shrub, often experiences very low air humidity at leaf temperatures over 10°C higher than mean air temperature. We determined to what degree this particular microclimate influenced photosynthetic performance, leaf conductance and water relations of non-irrigated and trickle-irrigated plants. Measurements were made at the end of the dry summer season in the sand plain lowland fynbos on the west coast of South Africa. Independent of water supply, plants showed a pronounced midday depression of gas exchange. While in non-irrigated plants leaf water potential dropped to ? 2.0 MPa around noon, it never fell below ?1.0 MPa in irrigated plants. On the other hand minimum pressure potential was similar in irrigated and non-irrigated plants. The latter showed higher turgor after rain, due to osmotic acclimation, which resulted from a reduction in maximum water volume. The main osmoticum was 1,5-anhydro-D-glucitol. Leaf temperature, directly or via the vapour pressure deficit between leaf and air (Δw), rather than plant water status, was the determinant of the midday depression of gas exchange. High Δw caused stomatal closure during times of saturating light, thus limiting photosynthetic CO₂ uptake and availability and enhancing the susceptibility for photoinhibition. This, as well as high leaf temperature per se, decreased the efficiency of photochemistry of photosystem II. Initial fluorescence remained constant until temperatures exceeded 35 °C, above which changes in fluorescence indicated both photoinhibition and heat stress. Unlike other fynbos plants, Protea acaulos could not use the improved soil water supply to increase carbon gain under hot summer condition.     

Nitrogen supply as a factor influencing photoinhibition and photosynthetic acclimation after transfer of shade-grown Solanum dulcamara to bright light

We have compared the ability of shadegrown clones of Solamum dulcamara L. from shade and sun habitats to acclimate to bright light, as a function of nitrogen nutrition before and after transfer to bright light. Leaves of S. dulcamara grown in the shade with 0.6 mM NO ₃ ^- have similar photosynthetic properties as leaves of plants grown with 12.0 mM NO ₃ ^- . When transferred to bright light for 1–2 d the leaves of these plants show substantial photoinhibition which is characterized by about 50% decrease in apparent quantum yield and a reduction in the rate of photosynthesis in air at light saturation. Photoinhibition of leaf photosynthesis is associated with reduction in the variable component of low-temperature fluorescence emission, and with loss of in-vitro electron transport, especially of photosystem II-dependent processes.We find no evidence for ecotypic differentiation in the potential for photosynthetic acclimation among shade and sun clones of S. dulcamara, or of differentiation with respect to nitrogen requirements for acclimation. Recovery from photoinhibition and subsequent acclimation of photosynthesis to bright light only occurs in leaves of plants provided with 12.0 mM NO ₃ ^- . In these, apparent quantum yield is fully restored after 14 d, and photosynthetic acclimation is shown by an increase in light-saturated photosynthesis in air, of light-and CO₂-saturated photosynthesis, and of the initial slope of the CO₂-response curve. The latter changes are highly correlated with changes in ribulose-bisphosphate-carboxylase activity in vitro. Plants supplied with 0.6 mM NO ₃ ^- show incomplete recovery of apparent quantum yield after 14 d, but CO₂-dependent leaf photosynthetic parameters return to control levels.Symbols and abbreviations F_o initial level of fluorescence at 77 K - F_m maximum level of fluorescence at 77 K - F_v variable components of fluorescence at 77 K (F_v=F_m-F_o) - PSI, PSII photosystem I and II, respectively - RuBP ribulose-1,5-bisphosphate - RuBPCase ribulose-1,5-bisphosphate carboxylase-oxygenase (EC 4.1.1.39)     

The seasonal pattern of CO2 exchange of Festuca rubra L. in a montane meadow community in Northern Germany

Summary Completely climatized cuvettes were used to follow the CO₂ gas exchange of red fescue (Festuca rubra L.), growing on a fertilized and an unfertilized plot, during a growing season from May through October. Objective of the study was to determine the effect of environmental factors on the seasonal CO₂ gas exchange.Gas exchange rates were calculated on the basis of leaf dry weight, surface area and chlorophyll content. Photosynthetic rates differed between the fertilized and unfertilized plants when based on leaf dry weight or leaf surface area but were similar when based on chlorophyll.Multiple regression analysis was used to related photosynthetic rates to radiation, temperature, water vapor concentration difference, chlorophyll content and time. A cubic regression equation based on daily radiation alone explained 85% of the variation for the fertilized plants and 87% of the variation for the unfertilized plants.During the growing season the unfertilized plants had a continual decline in their photosynthetic rates. The fertilized plants had high photosynthetic rates in the spring and in the fall.Light response curves indicated greater photosynthetic rates at light saturation as well as in the light limited portion of the light response curve for the fertilized plants. Photosynthetic rates of the fertilized plants were generally depressed during periods of warm temperature and high light intensity in June and July.Photosynthetic rates declined at temperatures above 24°C. The decline was greater for the more mesomorphic fertilized plants. A similar response was noted to increasing water vapor difference, although it was difficult to separate from the temperature effect. Maximum photosynthetic rates were found between 14°C and 22°C, although there was considerable variation in the maximum rates.The effects of cutting (mowing) on the gas exchange were difficult to determine due to the interaction of the environmental factors.Chlorophyll content showed significant correlation with photosynthetic rates.     

Elevated CO<Subscript>2</Subscript> mitigates the adverse effects of drought on daytime net ecosystem CO<Subscript>2</Subscript> exchange and photosynthesis in a Florida scrub-oak ecosystem

Drought is a normal, recurrent feature of climate. In order to understand the potential effect of increasing atmospheric CO₂ concentration (C _a) on ecosystems, it is essential to determine the combined effects of drought and elevated C _a (EC) under field conditions. A severe drought occurred in Central Florida in 1998 when precipitation was 88 % less than the average between 1984 and 2002. We determined daytime net ecosystem CO₂ exchange (NEE) before, during, and after the drought in the Florida scrub-oak ecosystem exposed to doubled C _a in open-top chamber since May 1996. We measured diurnal leaf net photosynthetic rate (P _N) of Quercus myrtifolia Willd, the dominant species, during and after the drought. Drought caused a midday depression in NEE and P _N at ambient CO₂ concentration (AC) and EC. EC mitigated the midday depression in NEE by about 60 % compared to AC and the effect of EC on leaf P _N was similar to its effect on NEE. Growth in EC lowered the sensitivity of NEE to air vapor pressure deficit under drought. Thus EC would help the scrub-oak ecosystem to survive the consequences of the effects of rising atmospheric CO₂ on climate change, including increased frequency of drought, while simultaneously sequestering more anthropogenic carbon.