We examined the carbon budget of young winter wheat plants and their associated microorganisms as affected by a doubling of the atmospheric CO2 concentration (700 µmol mol-1). Plants were grown hydroponically in pre-sterilised sand at a controlled irradiance and temperature regime. Net photosynthesis (PN) and respiration (RD) rates of roots and shoots were measured continuously, plant growth and carbon distribution in the plant-root medium-associated microorganism system were determined destructively in interval-based analyses. PN in elevated CO2 grown plants (EC) was 123% of that in the control (AC) plants when averaged over the whole life span (39-d-old plants, 34 d in EC), but the percentage varied with the developmental stage being 115, 88, and 167% in the pretillering, tillering, and posttillering phase, respectively. There was a transient depression of PN, higher amplitude of day/night fluctuations of the chloroplast starch content, and depression of carbon content in rhizosphere of EC plants during the period of tillering. After 34 d in EC, carbon content in shoots, roots, and in rhizodepositions was enhanced by the factors 1.05, 1.28, and 1.96, respectively. Carbon partitioning between above and belowground biomass was not affected by EC, however, proportionally more C in the belowground partitioning was allocated into the root biomass. Carbon flow from roots to rhizodepositions and rhizosphere microflora was proportional to PN; its fraction in daily assimilated carbon decreased from young (17%) to order (3-4%) plants. and H. Šantrůčková ... [et al.].
Life and research results of Pavel Siffel, a talented but untimely deceased Czech scientist in photosynthesis, are reviewed. He studied biophysics and physiology of chlorophyll, its complexes with proteins, their absorption and fluorescence spectra, activities in mutants and transformants, dealt with chlorophyll biosynthesis and protochlorophyllide photoreduction, pigments in plants grown at CO2 deficiency and under simulated acid rain, with changes accompanying leaf and plant development, photobleaching, etc. He participated in construction of specialised spectrofluorometers, finally he built the kinetic spectrophotometer SpeKin. and J. Květoň ... [et al.].
Environmental factors that induce spatial heterogeneity of stomatal conductance, gs, called stomatal patchiness, also reduce the photochemical capacity of CO2 fixation, yet current methods cannot distinguish between the relative effect of stomatal patchiness and biochemical limitations on photosynthetic capacity. We evaluate effects of stomatal patchiness and the biochemical capacity of CO2 fixation on the sensitivity of net photosynthetic rate (PN) to stomatal conductance (gs), θ (θ = δP N/gs). A qualitative model shows that stomatal patchiness increases the sensitivity θ while reduced biochemical capacity of CO2 fixation lowers θ. We used this feature to distinguish between stomatal patchiness and mesophyll impairments in the photochemistry of CO2 fixation. We compared gas exchange of sunflower (Helianthus annuus L.) plants grown in a growth chamber and fed abscisic acid, ABA (10-5 M), for 10 d with control plants (-ABA). PN and gs oscillated more frequently in ABA-treated than in control plants when the leaves were placed into the leaf chamber and exposed to a dry atmosphere. When compared with the initial CO2 response measured at the beginning of the treatment (day zero), both ABA and control leaves showed reduced PN at particular sub-stomatal CO2 concentration (ci) during the oscillations. A lower reduction of P N at particular g s indicated overestimation of ci due to stomatal patchiness and/or omitted cuticular conductance, gc. The initial period of damp oscillation was characterised by inhibition of chloroplast processes while stomatal patchiness prevailed at the steady state of gas exchange. The sensitivity θ remained at the original pre-treatment values at high gs in both ABA and control plants. At low gs, θ decreased in ABA-treated plants indicating an ABA-induced impairment of chloroplast processes. In control plants, gc neglected in the calculation of gs was the likely reason for apparent depression of photosynthesis at low gs. and J. Šantrůček ... [et al.].