Plants differ in how much the response of net photosynthetic rate
(PN) to temperature (T) changes with the T during leaf development, and also in the biochemical basis of such changes in response. The amount of photosynthetic acclimation to T and the components of the photosynthetic system involved were compared in Arabidopsis thaliana and Brassica oleracea to determine how well A. thaliana might serve as a model organism to study the process of photosynthetic acclimation to T. Responses of single-leaf gas exchange and chlorophyll fluorescence to CO2 concentration measured over the range of 10-35 °C for both species grown at 15, 21, and 27 °C were used to determine the T dependencies of maximum rates of carboxylation (VCmax), photosynthetic electron transport (Jmax), triose phosphate utilization rate (TPU), and mesophyll conductance to carbon dioxide (g'm). In A. thaliana, the optimum T of PN at air concentrations of CO2 was unaffected by this range of growth T, and the T dependencies of VCmax, Jmax, and g'm were also unaffected by growth T. There was no evidence of TPU limitation of PN in this species over the range of measurement conditions. In contrast, the optimum T of PN increased with growth T in B. oleracea, and the T dependencies of VCmax, Jmax, and g'm, as well as the T at which TPU limited PN all varied significantly with growth T. Thus B. oleracea had much a larger capacity to acclimate photosynthetically to moderate T than did A. thaliana.
Leaves developed at high irradiance (I) often have higher photosynthetic capacity than those developed at low I, while leaves developed at elevated CO2 concentration [CO2] often have reduced photosynthetic capacity compared with leaves developed at lower [CO2]. Because both high I and elevated [CO2] stimulate photosynthesis of developing leaves, their contrasting effects on photosynthetic capacity at maturity suggest that the extra photosynthate may be utilized differently depending on whether I or [CO2] stimulates photosynthesis. These experiments were designed to test whether relationships between photosynthetic income and the net accumulation of soluble protein in developing leaves, or relationships between soluble protein and photosynthetic capacity at full expansion differed depending on whether I or [CO2] was varied during leaf development. Soybean plants were grown initially with a photosynthetic photon flux density (PPFD) of 950 µmol m-2 s-1 and 350 µmol [CO2] mol-1, then exposed to [CO2] ranging from 135 to 1400 µmol mol-1 for the last 3 d of expansion of third trifoliolate leaves. These results were compared with experiments in which I was varied at a constant [CO2] of 350 µmol mol-1 over the same developmental period. Increases in area and dry mass over the 3 d were determined along with daily photosynthesis and respiration. Photosynthetic CO2 exchange characteristics and soluble protein content of leaves were determined at the end of the treatment periods. The increase in leaflet mass was about 28 % of the dry mass income from photosynthesis minus respiration, regardless of whether [CO2] or I was varied, except that very low I or [CO2] increased this percentage. Leaflet soluble protein per unit of area at full expansion had the same positive linear relationship to photosynthetic income whether [CO2] or I was varied. For variation in I, photosynthetic capacity varied directly with soluble protein per unit area. This was not the case for variation in [CO2]. Increasing [CO2] reduced photosynthetic capacity per unit of soluble protein by up to a factor of 2.5, and photosynthetic capacity exhibited an optimum with respect to growth [CO2]. Thus CO2 did not alter the relationship between photosynthetic income and the utilization of photosynthate in the net accumulation of soluble protein, but did alter the relationship between soluble protein content and photosynthetic characteristics in this species.
The fundamental cause of down-regulation of photosynthesis at elevated carbon dioxide concentration (EC) is thought to be a slower rate of utilization of saccharides than their stimulated rate of production, but there are few studies directly supporting this idea under field conditions. We hypothesized that within Brassica oleracea, down-regulation would not occur in kohlrabi because it has a large sink for saccharides in an enlarged stem, but would occur in collards, which lack this sink. Field tests were consistent with this hypothesis. In collards, the degree of down-regulation of photosynthesis in plants grown at EC varied depending on the daily integral of photosynthetically active radiation (PAR) of the day prior to the measurement of photosynthetic capacity, as did leaf saccharide content. However, EC did not result in lower leaf contents of chlorophyll, soluble protein, ribulose-1,5-bisphosphate carboxylase, or nitrate in collards, nor was there any evidence of a triose phosphate utilization rate limiting photosynthesis. Experiments in controlled environment chambers confirmed that there was a threshold response for the down-regulation of photosynthesis in collards at EC to the PAR of the previous day, with down-regulation only occurring above a minimum daily integral of PAR. Down-regulation of photosynthesis could be induced in plants grown at ambient carbon dioxide by a single night at low temperature or by a single day with high PAR and EC. In the controlled environment study, the degree of down-regulation of photosynthesis was highly correlated with leaf glucose, fructose, and sucrose contents, and less well correlated with starch content. Hence down-regulation of photosynthesis at EC in collards in the field represented feedback inhibition from the accumulation of soluble saccharides and day-to-day variation in its occurrence was predictable from the weather. and J. A. Bunce, R. C. Sicher.
We hypothesized that decreased stomatal conductance (gs) at elevated CO2 might decrease transpiration (E), increase leaf water potential (ΨW), and thereby protect net photosynthesis rate (PN) from heat damage in maize (Zea mays L) seedlings. To separate long-term effects of elevated CO2, plants grew at either ambient CO2 or elevated CO2. During high-temperature treatment (HT) at 45°C for 15 min, leaves were exposed either to ambient CO2 (380 μmol mol-1) or to elevated CO2 (560 μmol mol-1). HT reduced PN by 25 to 38% across four CO2 combinations. However, the gs and E did not differ among all CO2 treatments during HT. After returning the leaf temperature to 35°C within 30 min, gs and E were the same or higher than the initial values. Leaf water potential (ΨW) was slightly lower at ambient CO2, but not at elevated CO2. This study highlighted that elevated CO2 failed in protecting PN from 45°C via decreasing gs and ΨW., M. N. Qu, J. A. Bunce, Z. S. Shi., and Obsahuje bibliografii
Controlled environment chamber and glasshouse studies were conducted on six herbaceous annual species grown at 350 (AC) and 700 (EC) μmol(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 (PN) measured at saturating PPFD. It was also determined whether acclimation in PN 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 PN 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. and J. A. Bunce, L. H. Ziska.
C3 photosynthesis at high light is often modeled by assuming limitation by the maximum capacity of Rubisco carboxylation (VCmax) at low CO2 concentrations, by electron transport capacity (Jmax) at higher CO2 concentrations, and sometimes by
triose-phosphate utilization rate at the highest CO2 concentrations. Net photosynthetic rate (PN) at lower light is often modeled simply by assuming that it becomes limited by electron transport (J). However, it is known that Rubisco can become deactivated at less than saturating light, and it is possible that PN at low light could be limited by the rate of Rubisco carboxylation (VC) rather than J. This could have important consequences for responses of PN to CO2 and temperature at low light. In this work, PN responses to CO2 concentration of common bean, quinoa, and soybean leaves measured over a wide range of temperatures and PPFDs were compared with rates modeled assuming either VC or J limitation at limiting light. In all cases, observed rates of PN were better predicted by assuming limitation by VC rather than J at limiting light both below and above the current ambient CO2. One manifestation of this plant response was that the relative stimulation of PN with increasing the ambient CO2 concentration from 380 to 570 µmol mol-1 did not decrease at less than saturating PPFDs. The ratio of VC to VCmax at each lower PPFD varied linearly with the ratio of PN at low PPFD to PN at high PPFD measured at 380 µmol(CO2) mol-1 in all cases. This modification of the standard C3 biochemical model was much better at reproducing observed responses of light-limited PN to CO2 concentrations from
pre-industrial to projected future atmospheric concentrations., J. A. Bunce., and Obsahuje bibliografii
Independent short-term effects of photosynthetic photon flux density (PPFD) of 50-400 µmol m-2 s-1, external CO2 concentration (C a) of 85-850 cm3 m-3, and vapor pressure deficit (VPD) of 0.9-2.2 kPa on net photosynthetic rate (PN), stomatal conductance (gs), leaf internal CO2 concentration (Ci), and transpiration rates (E) were investigated in three cacao genotypes. In all these genotypes, increasing PPFD from 50 to 400 µmol m-2 s-1 increased PN by about 50 %, but further increases in PPFD up to 1 500 µmol m-2 s-1 had no effect on PN. Increasing Ca significantly increased PN and Ci while gs and E decreased more strongly than in most trees that have been studied. In all genotypes, increasing VPD reduced PN, but the slight decrease in gs and the slight increase in Ci with increasing VPD were non-significant. Increasing VPD significantly increased E and this may have caused the reduction in PN. The unusually small response of gs to VPD could limit the ability of cacao to grow where VPD is high. There were no significant differences in gas exchange characteristics (gs, Ci, E) among the three cacao genotypes under any measurement conditions. and F. C. Baligar ... [et al.].
In tomato {Lycopersicon esculentum L.) plants, net carbon dioxide exchange rate (P]si) response curves to both irradiance (/) and short-term [CO2] were similar for plants grown at both 350 and 700 cm3(C02) m'^. However, water vapor conductance (gHjo) of plants grown at high [CO2] was less sensitive to short term [CO2] variations, when measured at low vapor pressure difference, and was larger than the conductance of "ambient [CO2]" plants when both were exposed to high [CO2]. Pn and gHjO under high I increased with temperature over the range 18 to 32 °C. of plants grown in both [CO2] treatments increased at most about 25 % from 350 to 700 cm3 m-3 at 18 and 25 °C, and decreased when exposed to 1000 cm^ m'^ at these temperatures. Thus increasing atmospheric [CO2] might not increase P^ by as much as expected and water use of crops might not decrease.
a1_The carbon dioxide concentration in free air carbon dioxide enrichment (FACE) systems typically has rapid fluctuations. In our FACE system, power spectral analysis of CO2 concentration measured every second with an open path analyzer indicated peaks in variation with a period of about one minute. I used
open-top chambers to expose cotton and wheat plants to either a constant elevated CO2 concentration of 180 μmol mol-1 above that of outside ambient air, or to the same mean CO2 concentration, but with the CO2 enrichment cycling between about 30 and 330 μmol mol-1 above the concentration of outside ambient air, with a period of one minute. Three short-term replicate plantings of cotton were grown in Beltsville, Maryland with these CO2 concentration treatments imposed for 27-day periods over two summers, and one winter wheat crop was grown from sowing to maturity. In cotton, leaf gas-exchange measurements of the continuously elevated treatment and the fluctuating treatment indicated that the fluctuating CO2 concentration treatment consistently resulted in substantial down-regulation of net photosynthetic rate (PN) and stomatal conductance (gs). Total shoot biomass of the vegetative cotton plants in the fluctuating CO2 concentration treatment averaged 30% less than in the constantly elevated CO2 concentration treatment at 27 days after planting. In winter wheat, leaf gas-exchange measurements also indicated that down-regulation of PN and gs occurred in flag leaves in the fluctuating CO2 concentration treatment, but the effect was not as consistent in other leaves, nor as severe as found in cotton. However, wheat grain yields were 12% less in the fluctuating CO2 concentration treatment compared with the constant elevated CO2 concentration treatment., a2_Comparison with wheat yields in chambers without CO2 addition indicated a nonsignificant increase of 5% for the fluctuating elevated CO2 concentration treatment, and a significant increase of 19% for the constant elevated treatment. The results suggest that treatments with fluctuating elevated CO2 concentrations could underestimate plant growth at projected future atmospheric CO2 concentrations., J. A. Bunce., and Obsahuje bibliografii
Some studies of responses of plants to elevated concentrations of carbon dioxide (EC) added CO2 only in the daytime, while others supplied CO2 continuously. I tested whether these two methods of EC treatments produced differences in the seed yield of soybeans. Tests were conducted for four growing seasons, using open top chambers, with soybeans rooted in the ground in field plots. One third of the chambers were flushed with air at the current ambient [CO2] (AC), one third had [CO2] 350 µmol mol-1 above ambient during the daytime (ECd), while one third had [CO2] 350 µmol mol-1 above ambient for 24 h per day (ECdn). ECdn increased seed yield by an average of 62 % over the four years compared with the AC treatment, while ECd increased seed yield by 34 %. Higher seed yield for ECdn compared with ECd occurred each year. In comparing years, the relative yield disadvantage of ECd decreased with increasing overall seed yield. On days with high water vapor pressure deficits, soybean canopies with ECd had smaller midday extinction coefficients for photosynthetically active radiation than canopies with ECdn, because of a more vertical leaf orientation. Hence the seed yield of soybean at EC varied depending on whether EC was also provided at night, with much greater yield stimulation for ECdn than for ECd in some years.