High temperature is a common constraint during anthesis and grain-filling stages of wheat leading to huge losses in yield. In order to understand the mechanism of heat tolerance during monocarpic senescence, the present study was carried out under field conditions by allowing two well characterized Triticum aestivum L. cultivars differing in heat tolerance, Hindi62 (heat-tolerant) and PBW343 (heat-susceptible), to suffer maximum heat stress under late sown conditions. Senescence was characterized by measuring photosynthesis related processes and endoproteolytic activity during non-stress environment (NSE) as well as heat-stress environment (HSE). There was a faster rate of senescence under HSE in both the genotypes. Hindi62, having pale yellow flag leaf with larger area, maintained cooler canopy under high temperatures than PBW343. The tolerance for high temperature in Hindi62 was clearly evident in terms of slower green-leaf area degradation, higher stomatal conductance, higher stability in maximum PSII efficiency, Rubisco activity and Rubisco content than PBW343. Both the genotypes exhibited lower endopeptidase activity under HSE as compared to NSE and this difference was more apparent in Hindi62. Serine proteases are the predominant proteases responsible for protein degradation under NSE as well as HSE. Flag leaf of both the genotypes exhibited high-molecular-mass endoproteases (78 kDa and 67 kDa) isoforms up to full grain maturity which were inhibited by specific serine protease inhibitor in both the environments. In conclusion, the heat-tolerant Hindi62 exhibited a slower rate of senescence than the heat-susceptible PBW343 during HSE, which may contribute towards heat stability. and S. Chauhan ... [et al.].
The coffee plant is native to shaded environments and its seedlings are often produced in shaded nurseries. However, some nursery managers, in an effort to improve the acclimation of seedlings to field conditions after transplantation, produce seedlings in full sun exposure. In this study, the morphological and physiological parameters of arabica coffee (Coffea arabica) seedlings produced in full sun (T1) and in shade (T2) were examined. The biomass accumulation and relative growth rate of T1 and T2 seedlings were similar. The T1 seedlings had less biomass allocation to shoots, a lower leaf mass ratio and a lower leaf area ratio; however, they had a greater net assimilation rate (rate of increase in plant mass per unit leaf area), which was associated with a greater net photosynthetic rate. There were no alterations in the concentrations of total chlorophylls or in the chlorophyll a/b ratio when comparing T1 and T2 seedlings. No indications of photoinhibition or photooxidative damage were observed in the T1 plants, which were shown to have a more robust antioxidant system than the T2 plants. Seedlings transferred from shade to full sun (T3) were not capable of utilising the incident extra light to fix CO2. These seedlings showed a remarkable nocturnal retention of zeaxanthin and a significantly increased deepoxidation state of the xanthophyll cycle, even at predawn, but the activity of antioxidant enzymes was lower than in the T1 and T2 plants. Despite the acclimation capacity of T3 seedlings to the new light environment, they exhibited chronic photoinhibition and considerable photooxidative damage throughout the seven days following the transfer to full sun exposure. We further discuss the practical implications of producing coffee seedlings in full sunlight and under shade. and G. A. B. K. Moraes ... [et al.].
On the occasion of the 50th anniversary of the international journal Photosynthetica in 2017 we briefly report on the establishment of this journal and on Dr. Zdeněk Šesták, the renowned researcher of photosynthesis processes who, in cooperation with the Czechoslovak Academy of Sciences, founded this essential science journal in Prague in 1967., H. K. Lichtenthaler., Obsahuje bibliografii, and Ozvláštněné číslování stránek článku 1-6. teprve na ně se napojuje pokračování stránkování navazující na 1. číslo časopisu
Accumulation and distribution of zinc within Miscanthus x giganteus plants grown on elevated Zn concentrations and their photosynthetic performance were investigated. High concentrations of Zn in soils caused an increase of its concentrations in all plant organs. The bioconcentration factor, bioaccumulation factor, and translocation factor were lower than one indicating that M. x giganteus is an excluder plant species. Excessive Zn induced visible leaf damage, i.e. chlorosis and necrosis, only in the oldest leaves, pointing to Zn accumulation. Elevated amounts of Zn in leaves significantly lowered the photosynthetic rate, transpiration rate, stomatal conductance, intercellular CO2 concentrations, parameters of chlorophyll a fluorescence, and chlorophyll b content. Despite Zn excess in leaves, there was no severe reduction in the maximal quantum yield of PSII photochemistry, indicating a high photosynthetic capacity, high tolerance to elevated Zn concetrations, and ability of M. x giganteus to grow on Zn-contaminated soils., G. Andrejić, G. Gajić, M. Prica, Ž. Dželetović, T. Rakić., and Obsahuje bibliografii
Zinc is a critical mineral nutrient that protects plant cells from salt-induced cell damage. We tested whether the application of Zn at various concentrations [0, 5, 10, or 20 mg kg-1(soil)] would protect almond (Prunus amygdalus) seedlings subjected to salt stress (0, 30, 60, or 90 mM NaCl). All concentrations of Zn, particularly the application of 10 and 20 mg kg-1, increased the net photosynthetic rate, stomatal conductance, the maximal efficiency of PSII photochemistry, and a proline content in almond seedlings grown under salt stress; 20 mg(Zn) kg-1 was the most effective concentration. The activity of superoxide dismutase showed a significant increase under salinity stress and Zn application. The catalase activity decreased in the salt-treated seedlings, but recovered after the Zn treatment. Our results proved the positive effects of Zn on antioxidant enzyme activity scavenging the reactive oxygen species produced under salt stress., A. Amiri, B. Baninasab, C. Ghobadi, A. H. Khoshgoftarmanesh., and Obsahuje seznam literatury