We examined effects of late-season heat stress (L-SHS) on chlorophyll (Chl) fluorescence parameters and yield of bread wheat as well as roles of phosphate bio-fertilizer (PB-F) and Zn and B to compensate for the likely effects of heat stress. Factors were planting date (21 November and 5 January to coincide with grain filling to L-SHS) as the main factor, no inoculation (control) and inoculation of the seeds with PB-F as the sub-factor, and foliar application of water (control), Zn, B, and Zn + B as 3 L ha-1 as
sub-sub factor. Results revealed that L-SHS reduced maximal quantum yield of PSII photochemistry, effective quantum yield of PSII photochemistry, efficiency of PSII in the light-adapted state, and the grain yield. Moreover, L-SHS increased the nonphotochemical quenching. The PB-F mitigated the effects of L-SHS on Chl fluorescence, yield, and yield components. Among nutrients, the combined Zn + B was more effective in reducing the effects of L-SHS than that of Zn and B alone. Nevertheless, there was an interaction between foliar nutrients application and PB-F, suggesting that Zn application alone had a profound influence on improving Chl fluorescence parameters and increased yield in combination with PB-F., H. R. Eisvand, H. Kamaei, F. Nazarian., and Obsahuje bibliografii
Chloroplasts utilize photons from solar radiation to synthesize energy-rich molecules of ATPs and NADPHs, which are further used in active cellular processes. Multiprotein complexes (MPCs), including photosystems (PSII and PSI), and the cellular architecture responsible for generation of the proton motive force and the subsequent photophosphorylation, mediate the task of ATP and NADPH synthesis. Both photosystems and other multiprotein assemblies are embedded in thylakoid membranes. Advances in techniques used to study structural biology, biophysics, and comparative genomics and proteomics have enabled us to gain insights of structure, function, and localization of each individual component of the photosynthetic apparatus. An efficient coordination among MPCs is essential for normal functioning of photosynthesis, but there are various stressors that might directly or indirectly interact with photosynthetic components and processes. Cadmium is one of the toxic heavy metals that interact with photosynthetic components and damage photosystems and other MPCs in thylakoids. In plants, iron deficiency shows similar symptoms as those caused by Cd. Our article provides a general overview of chloroplast structure and a critical account of Cd-induced changes in photosystems and other MPCs in thylakoids, and suggests the possible mechanisms involved in mediating these changes. The connection between Cd-induced Fe deficiency and the elevated Cd toxicity under the Fe-deficient condition was also discussed., H. Bashir, M. I. Qureshi, M. M. Ibrahim, M. Iqbal., and Obsahuje seznam literatury
Glechoma longituba (Nakai) Kupr. is a perennial shade plant with pharmaceutical importance. The aim of this study was to investigate the effects of light intensity on the growth, photosynthesis, and accumulation of secondary metabolites in G. longituba grown under six different light environments. The high light intensity decreased the leaf size, specific leaf area, and aboveground dry mass, the number of grana per chloroplast, the number of lamella per granum, the thickness of the grana, the apparent quantum efficiency, the chlorophyll (Chl) content, the concentrations of ursolic and oleanolic acid. The high light increased the stomatal density, the stoma size, the number of chloroplast per a cell, the chloroplast size, the dark respiration rate, the light saturation point, the light compensation point, and the Chl a/b ratio. With the reduction in the light intensity, the light-saturated net photosynthetic rate, the aerial dry mass per plant, and the yields of ursolic and oleanolic acid decreased after an initial increase, peaking at 16 and 33% of sunlight levels. Overall, the 16 and 33% irradiance levels were the most efficient in improving the yields and qualities of the medicinal plant. The lower light demand and growth characteristics suggest that G. longituba is an extremely
shade-tolerant plant and that appropriate light intensity management might be feasible to obtain higher yields of secondary metabolites in agricultural management., L. X. Zhang, Q. S. Guo, Q. S. Chang, Z. B. Zhu, L. Liu, Y. H. Chen., and Obsahuje bibliografii
Tomato (Lycopersicon esculentum Mill. cv. Pearson) plants were grown in growth chambers for 25 days with cadmium (Cd) and then exposed briefly to ozone (O3). Gas exchange, chlorophyll a fluorescence, and pigment composition were analysed in leaves at the end of the treatment to assess the effects of a single pollutant and their combination on photosynthesis. The CO2 assimilation rate was dramatically reduced in plants subjected to the combined treatment, while the single effect of Cd appeared less severe than that of O3. The decline of CO2 photoassimilation found in all
O3-exposed plants was attributed to both stomatal and nonstomatal limitations. Tomato plants seemed to detoxify Cd to a great extent, but this resulted in growth suppression. In response to O3 exposure, the plants protected their photosystems by heat dissipation of excess energy via the xanthophyll cycle. Cd combined with O3 affected adversely this cycle resulting in an increase in photosynthetic performance under the same experimental light conditions., E. Degl’Innocenti, A. Castagna, A. Ranieri, L. Guidi., and Obsahuje bibliografii
The chilling and light stresses were experimentally created to explore photosynthesis of Fraxinus mandshurica seedlings in northeast China. Net photosynthetic rate, stomatal conductance, and transpiration rate decreased significantly with the decline of temperature and light. Significant interaction effects of light and chilling were observed on gas exchange of photosynthesis. The minimal fluorescence yield of the dark-adapted state (F0) increased with increasing light and decreasing temperature. Both high and low light stresses induced the decreases of the maximal quantum yield of PSII photochemistry (Fv/Fm), photochemical quenching coefficient (qP), nonphotochemical quenching (NPQ), and electron transport rate. Decline of Fv/Fm and increased F0 were observed under decreasing temperatures. Decreased NPQ and qP at frost temperature suggest that F. mandschurica failed to dissipate excess light energy. No interactive effects of chilling and light on chlorophyll fluorescence parameters suggests that F. mandschurica seedlings might be adapted to combined stresses of light and chilling., X. F. Li, L. Jin, C. Y. Zhu, Y. J. Wen, Y. Wang., and Obsahuje bibliografii
The impact of drought stress (DS) on eight Eurasian and North African genotypes of wild barley (Hordeum spontaneum) was evaluated by analysis of chlorophyll (Chl) a fluorescence fast induction curves using the JIP-test. Three-week-old, pot-grown plants were exposed to a DS treatment by withholding water for nine days. The genotype-specific impairment of the functionality of the photosynthetic electron transport chain was quantified using the relative decline of the performance indices (PIabs and PItot), two key parameters of the JIP-test. The genotypes showing the highest (HOR10164) and lowest (HOR10710) relative PIs under DS were subjected to additional experiments, including measurements of leaf gas exchange, water status, pigment content, key enzyme activity, and protein abundance. The genotypes showed a specific profile of DS-mediated inhibition of photosynthesis, associated with higher relative leaf water contents in HOR10164 at the end of the treatment. Whereas decreased photosynthetic rate in HOR10164 was mainly caused by stomatal closure, nonstomatal limitations (decreased Rubisco content and activity) were detected in HOR10710. Additional genotype specific features were the upregulation of the NADP-malate dehydrogenase in HOR10164 and a decreased fraction of QA-reducing reaction centers in HOR10710., C. Jedmowski, S. Bayramov, W. Brüggemann., and Obsahuje bibliografii
The rare and endangered plant, Begonia fimbristipula, shows red and green phenotypes, differentiated by a coloration of the abaxial leaf surface. In this study, we compared morphological and physiological traits of both phenotypes. The results showed that the red phenotype contained a significantly higher chlorophyll content, closer arrangement of chloroplasts, and a more developed grana. In addition, the red phenotype transferred significantly more light energy into the electron transport during the photoreaction. Similarly, the maximum photosynthetic rate, instantaneous water-use and light-use efficiencies of the red B. fimbristipula were all significantly higher than those of the green individuals. The differentiation between these two phenotypes could be caused by their different survival strategies under the same conditions; epigenetic variations may be in some correlation with this kind of phenotype plasticity. Red B. fimbristipula has an advantage in resource acquisition and utilization and possesses a better self-protection mechanism against changes in environmental conditions, therefore, it might adapt better to global climate change compared to the green phenotype. Further studies on the possible epigenetic regulation of those phenotypic differentiations are needed., Y. Wang, L. Shao, J. Wang, H. Ren, H. Liu, Q. M. Zhang, Q. F. Guo, X. W. Chen., and Seznam literatury
In many plant species that remain leafless part of the year, CO2 fixation occurring in green stems represents an important carbon gain. Traditionally, a distinction has been made between stem photosynthesis and corticular photosynthesis. All stem photosynthesis is, sensu stricto, cortical, since it is carried out largely by the stem cortex. We proposed the following nomenclature: stem net photosynthesis (SNP), which includes net CO2 fixation by stems with stomata in the epidermis and net corticular CO2 fixation in suberized stems, and stem recycling photosynthesis (SRP), which defines CO2 ling in suberized stems. The proposed terms should reflect differences in anatomical and physiological traits. SNP takes place in the chlorenchyma below the epidermis with stomata, where the net CO2 uptake occurs, and it resembles leaf photosynthesis in many characteristics. SRP is found in species where the chlorenchyma is beneath a
well-developed stomata-free periderm and where reassimilation of internally respired CO2 occurs. SNP is common in plants from desert ecosystems, rates reaching up to 60% of the leaf photosynthetic rate. SRP has been demonstrated in trees from temperate forests and it offsets partially a carbon loss by respiration of stem nonphotosynthetic tissues. Reassimilation can vary between 7 and 123% of respired CO2, the latter figure implying net CO2 uptake from the atmosphere. Both types of stem photosynthesis contribute positively to the carbon economy of the species, in which they occur; they are advantageous to the plant because they allow the maintenance of physiological activity during stress, an increase of integrated water use efficiency, and they provide the carbon source used in the production of new organs., E. Ávila, A. Herrera, W. Tezara., and Obsahuje bibliografii
Differences in maximal yields of chlorophyll variable fluorescence (Fm) induced by single turnover (ST) and multiple turnover (MT) excitation are as great as 40%. Using mutants of Chlamydomonas reinhardtii we investigated potential mechanisms controlling Fm above and beyond the QA redox level. Fm was low when the QB binding site was occupied by PQ and high when the QB binding site was empty or occupied by a PSII herbicide. Furthermore, in mutants with impaired rates of plastoquinol reoxidation, Fm was reached rapidly during MT excitation. In PSII particles with no mobile PQ pool, Fm was virtually identical to that obtained in the presence of PSII herbicides. We have developed a model to account for the variations in maximal fluorescence yields based on the occupancy of the QB binding site. The model predicts that the variations in maximal fluorescence yields are caused by the capacity of secondary electron acceptors to reoxidize QA-., O. Prášil, Z. S. Kolber, P. G. Falkowski., and Obsahuje bibliografické odkazy