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The (11Bu+) energy of synthetic 15-cis β-carotene exhibits a linear dependence on (n2-1)/(n2+2) in non-polar and polar solvents; in this it is similar to (that of) all-trans β-carotene. The point of intersection is at (n2-1)/(n2+2) = 0.3 for both isomers. The microenvironment of 15-cis β-carotene in the Photosystem II reaction center was established as having a mean refractive index 1.473. Persistent spectral hole burning with a very broad (≈30 nm) hole observed around 500 nm (corresponding to an extremely short excited lifetime τ ≈9 fs) indicates that 15-cis β-carotene has/displays very efficient photoprotective quenching.
The influence of aphid feeding on chlorophyll a fluorescence in the leaves of four cultivated hazel cultivars, with different levels of resistance to filbert aphid (Myzocallis coryli Goetze), was studied. The maximum effect of photosystem reaction measured on dark-adapted hazel leaves (Fv/Fm parameter) and maximum efficiency of photon energy PAR conversion to chemical energy in light conditions (Y parameter) were estimated twice, in the leaves of four hazel cultivars with different levels of resistance to filbert aphid, using a fluorometer PAM- 2000 by Walz GmbH – Germany. The analysis of changes of these parameters showed that aphid feeding caused a reaction in all tested cultivars. The most visible reduction of the Fv/Fm and Y values as a result of aphid feeding was observed in the cultivars ‘Cud z Bollwiller’ and ‘Olbrzymi z Halle’, numerously colonized by aphids. A smaller number of aphids found on the leaves of more resistant cultivars – ‘Kataloński’ and ‘Lamberta Biały’, caused a weaker response of plants and a smaller decline in the value of this parameter. ‘Cud z Bollwiller’ cultivar showed higher tolerance than other tested cultivars to stress caused by the feeding of sucking insects. The Fv/Fm and Y parameters can be regarded as reliable indexes useful in diagnosing susceptibility of hazel cultivars to aphids, helpful in determining, for example, harmfulness thresholds.
Mitigation of man-made climate change, rapid depletion of readily available fossil fuel reserves and facing the growing energy demand that faces mankind in the near future drive the rapid development of economically viable, renewable energy production technologies. It is very likely that greenhouse gas emissions will lead to the significant climate change over the next fifty years. World energy consumption has doubled over the last twenty-five years, and is expected to double again in the next quarter of the 21st century. Our biosphere is at the verge of a severe energy crisis that can no longer be overlooked. Solar radiation represents the most abundant source of clean, renewable energy that is readily available for conversion to solar fuels. Developing clean technologies that utilize practically inexhaustible solar energy that reaches our planet and convert it into the high energy density solar fuels provides an attractive solution to resolving the global energy crisis that mankind faces in the not too distant future. Nature’s oxygenic photosynthesis is the most fundamental process that has sustained life on Earth for more than 3.5 billion years through conversion of solar energy into energy of chemical bonds captured in biomass, food and fossil fuels. It is this process that has led to evolution of various forms of life as we know them today. Recent advances in imitating the natural process of photosynthesis by developing biohybrid and synthetic “artificial leaves” capable of solar energy conversion into clean fuels and other high value products, as well as advances in the mechanistic and structural aspects of the natural solar energy converters, photosystem I and photosystem II, allow to address the main challenges: how to maximize solar-to-fuel conversion efficiency, and most importantly: how to store the energy efficiently and use it without significant losses. Last but not least, the question of how to make the process of solar energy conversion into fuel not only efficient but also cost effective, therefore attractive to the consumer, should be properly addressed.
To investigate the photoinhibition of photosynthesis in ‘Honeycrisp’ apple (Malus domestica Borkh. cv. Gala) leaves with zonal chlorosis, we compared pigments, CO₂ assimilation and chlorophyll (Chl) a fluorescence (OJIP) transient between chlorotic leaves and normal ones. Chl and carotenoids (Car) contents, Chl a/b ratio, and absorptance were lower in chlorotic leaves than in normal ones, whereas Car/Chl ratio was higher in the former. Although CO₂ assimilation and stomatal conductance were lower in chlorotic leaves, intercellular CO₂ concentration did not differ significantly between the two leaf types. Compared with normal leaves, chlorotic ones had increased deactivation of oxygen-evolving complexes (OEC), minimum fluorescence (Fₒ), dissipated energy, relative variable fluorescence at L-, W-, J- and I-steps, and decreased maximum fluorescence (Fm), maximum quantum yield for primary photochemistry (Fv/Fm or φRₒ/ABS), quantum yield for electron transport (ETₒ/ABS), quantum yield for the reduction of end acceptors of photosystem I (PSI) (uRo and REₒ/ABS), maximum amplitude of IP phase, amount of active photosystem II (PSII) reaction centers (RCs) per cross section (CS) and total performance index (PItot,abs). In conclusion, photoinhibition occurs at both the donor (i.e., the OEC) and the acceptor sides of PSII in chlorotic leaves. The acceptor side is damaged more severely than the donor side, which possibly is the consequence of over-reduction of PSII due to the slowdown of Calvin cycle. In addition to decreasing light absorptance by lowering Chl level, energy dissipation is enhanced to protect chlorotic leaves from photo-oxidative damage.
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