Twelve-year-old Norway spruce (Picea abies [L.] Karst.) were exposed to ambient (AC) or elevated (EC) [ambient + 350 μmol(CO2) mol-1] CO2 concentration [CO2] using the facilities of open-top-chambers (OTCs) and glass domes (GDs). A combination of gas exchange measurements and application of a biochemical model of photosynthesis were used for the evaluation of CO2 assimilation characteristics. Morphological change was assessed on the base of specific leaf area (SLA). Nitrogen (N) content in the assimilation apparatus was considered a main factor influencing the biochemical capacity. Three experiments confirm the hypothesis that an adjustment of photosynthetic capacity under EC is controlled by the combination of biochemical, morphological, and physiological feedback mechanisms. We observed periodicity of down-regulation of photosynthetic capacity (Experiment No. 1) during the vegetation seasons. In the spring months (May-June), i.e. during the occurrence of active carbon sink associated with the formation of new foliage, up-regulation (10-35 %) of photosynthetic capacity (PNsat) was observed. On the contrary, in the autumn months (September-October) down-regulation (25-35 %) of PNsat was recorded that was mainly associated with reduced carbon sink strength and biochemical change, i.e. decrease of N status (up to 32 %) and accumulation of saccharides (up to 72 %) in leaves. Different adjustments of photosynthetic activities were observed in current (C) and one-year-old (C-1) needles exposed to EC (Experiment No. 2). Strong down-regulation of PNsat and the diminution of the initial stimulation of photosynthetic rate (PNmax) was associated with decreases of both ribulose-1,5-bisphosphate carboxylase/oxygenase carboxylation activity (by 32 %) and RuBP regeneration (by 40 %). This performance was tightly correlated with the absence of active carbon sinks, decrease of N content, and starch accumulation in C-1 needles. Finally, different responses of sun- and shade-adapted needles to EC (Experiment No. 3) were associated with the balance between morphological and biochemical changes. Observed PNsat down-regulation (by 22 %) of exposed needles in EC was predominantly caused by effects of both higher assimilate accumulation and stronger N dilution, resulting from higher absolute photosynthetic rates and incident irradiances in the upper canopy. and O. Urban ... t al.].
The effect of ectomycorrhizal Pisolithus tinctorius (Pt) infection was studied on the growth and photosynthetic characteristics of Pinus densiflora seedlings grown at ambient (360 µmol mol-1, AC) and elevated (720 µmol mol-1, EC) CO2 concentrations. After 18 weeks, Pt inoculation had led to significantly increased dry mass and stem diameter of P. densiflora at both CO2 concentrations, relative to non-inoculated seedlings. Moreover, EC significantly increased the ectomycorrhizal development. The phosphate content in needles inoculated with Pt was about three times higher than without inoculation at both CO2 concentrations. The PAR saturated net photosynthetic rates (Psat) of P. densiflora inoculated with Pt were clearly higher than for control seedlings at both CO2 concentrations, and the maximum net photosynthetic rate (PN) at saturated CO2 concentration (Pmax) was higher than in controls. Moreover, the carboxylation efficiency (CE) and RuBP regeneration rate of the PN/Ci curve for P. densiflora inoculated with Pt were significantly higher than for non-inoculated seedlings at both CO2 concentrations, especially at EC. The water use efficiency (WUE) of seedlings inoculated with Pt grown at EC was significantly raised. Allocation of photosynthates to roots was greater in Pt inoculated pine seedlings, because of the enhanced activity of ectomycorrhiza associated with seedlings at EC. Moreover, PN of non-inoculated seedlings grown for 18 weeks at EC tended to be down regulated; in contrast, Pt inoculated seedlings showed no down-regulation at EC. The activity of ectomycorrhiza may therefore be enhanced physiological function related to water and phosphate absorption in P. densiflora seedlings at EC. and D. S. Choi ... [et al.].
In leaves of the mangrove species Avicennia germinans (L.) L. grown in salinities from 0 to 40 ‰, fluorescence, gas exchange, and δ13C analyses were done. Predawn values of Fv/Fm were about 0.75 in all the treatments suggesting that leaves did not suffer chronic photoinhibition. Conversely, midday Fv/Fm values decreased to about 0.55-0.60 which indicated strong down-regulation of photosynthesis in all treatments. Maximum photosynthetic rate (Pmax) was 14.58 ± 0.22 µmol m-2 s-1 at 0 ‰ it decreased by 21 and 37 % in plants at salinities of 10 and 40 ‰, respectively. Stomatal conductance (gs) was profoundly responsive in comparison to Pmax which resulted in a high water use efficiency. This was further confirmed by δ13C values, which increased with salinity. From day 3, after salt was removed from the soil solution, Pmax and gs increased up to 13 and 30 %, respectively. However, the values were still considerably lower than those measured in plants grown without salt addition.
Total in vitro activity of RuBPCO (ribulose-1,5-bisphosphate carboxylase/oxygenase) enzyme was assayed spectrophotometrically by the continuous measurement of 3-phosphoglycerate-dependent NADH oxidation in a coupled enzyme system. RuBPCO activities were found in the ranges 1.01-2.76 and 1.23-3.10 µmol(CO2) m-2 s- 1 in current Norway spruce needles growing in ambient (AC) and elevated (EC) CO2 concentration, respectively. RuBPCO activity in AC needles from the upper layer (U) was 11-15 % higher compared to those from the middle (M) layer, and even 44-56 % higher compared to the lower (L) layer of spruce crown. Over the vegetation season, we observed a highly significant decrease of RuBPCO activity in the EC-U needles from 3.10 (July) to 1.60 (October) µmol(CO2) m-2 s-1 as a consequence of downward feedback regulation. Moreover, this down-regulation was not caused by a non-specific decrease in total leaf nitrogen content. and M. Hrstka, O. Urban, M. V. Marek.
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