The occurrence of shade and drought stress either individually or simultaneously causes altered morphophysiological and molecular responses in crops. Nevertheless, responses of crop plants to combined shade and drought stress are unique as compared to those of individually occurring stress which urges need to study and identify distinctions, commonalities, and the interaction between responses of plants to these concurrent stress factors. In the present review, we outlined currently available knowledge on responses of plants to shade and drought stress on a shared as well as the unique basis and tried to find a common thread potentially underlying these responses. Then, we briefly described some plausible mitigation strategies to cope with these stresses along with future perspectives. A deeper insight into plant responses to co-occurring shade and drought stress will help us to generate crops with broad-spectrum stress tolerance and increased resilience to such stresses in high planting densities or intercropping systems, thus, ensuring food security.
In our earlier works, we have identified rate-limiting steps in the dark-to-light transition of PSII. By measuring chlorophyll a fluorescence transients elicited by single-turnover saturating flashes (STSFs) we have shown that in diuron-treated samples an STSF generates only F1 (< Fm) fluorescence level, and to produce the maximum (Fm) level, additional excitations are required, which, however, can only be effective if sufficiently long Δτ waiting times are allowed between the excitations. Biological variations in the half-rise time (Δτ1/2) of the fluorescence increment suggest that it may be sensitive to the physicochemical environment of PSII. Here, we investigated the influence of the lipidic environment on Δτ1/2 of PSII core complexes of Thermosynechococcus vulcanus. We found that while non-native lipids had no noticeable effects, thylakoid membrane lipids considerably shortened the Δτ1/2, from ~ 1 ms to ~ 0.2 ms. The importance of the presence of native lipids was confirmed by obtaining similarly short Δτ1/2 values in the whole T. vulcanus cells and isolated pea thylakoid membranes. Minor, lipid-dependent reorganizations were also observed by steady-state and time-resolved spectroscopic measurements. These data show that the processes beyond the dark-to-light transition of PSII depend significantly on the lipid matrix of the reaction center.
Large amounts of antibiotics and microplastics are used in daily life and agricultural production, which affects not only plant growth but also potentially the food safety of vegetables and other plant products. Fast detection of the presence of antibiotics and microplastics in leafy vegetables is of great interest to the public. In this work, a method was developed to detect sulfadiazine and polystyrene, commonly used antibiotics and microplastics, in vegetables by measuring and modeling photosystem II chlorophyll a fluorescence (ChlF) emission from leaves. Chrysanthemum coronarium L., a common beverage and medicinal plant, was used to verify the developed method. Scanning electron microscopy, transmission electron microscopy, and liquid chromatograph-mass spectrometer analysis were used to show the presence of the two pollutants in the samples. The developed kinetic model could describe measured ChlF variations with an average relative error of 0.6%. The model parameters estimated for the chlorophyll a fluorescence induction kinetics curve (OJIP) induction can differentiate the two types of stresses while the commonly used ChlF OJIP induction characteristics cannot. This work provides a concept to detect antibiotic pollutants and microplastic pollutants in vegetables based on ChlF.
To understand growth limitations of photosynthetic microorganisms, and to investigate whether batch growth or certain photosynthesis-related parameters predict a turbidostat (continuous growth at constant biomass concentration) growth rate, five green algal species were grown in a photobioreactor in batch and turbidostat conditions and their susceptibilities to photoinhibition of photosystem II as well as several photosynthetic parameters were measured. Growth rates during batch and turbidostat modes varied independently of each other; thus, a growth rate measured in a batch cannot be used to determine the continuous growth rate. Greatly different photoinhibition susceptibilities in tested algae suggest that different amounts of energy were invested in repair. However, photoinhibition tolerance did not necessarily lead to a fast growth rate at a moderate light intensity. Nevertheless, we report an inverse relationship between photoinhibition tolerance and minimum saturating irradiance, suggesting that fast electron transfer capacity of PSII comes with the price of reduced photoinhibition tolerance.
Apple rootstock seedling M.9-T337 was selected to explore the effect of drought stress. The findings indicated that the relative water content of both the leaf and soil gradually decreased with an increase in drought stress. The water-use efficiency of the leaves increased gradually but decreased sharply after 20 d of drought. Changes in the gas-exchange parameters and chlorophyll fluorescence parameters reflected the gradual decrease in the photosynthetic capacity of the plants with drought stress duration. Infrared thermal imaging showed significant temperature differences between the drought-stressed and control plants after 15 d of drought treatment. When irreversible damage occurred under drought stress, the crop water-stress index and relative water content of the leaf and soil were 0.7, 60.5, and 17.8%, respectively. Based on the results, we formulated a drought stress-grade standard. Further, we established that the best time for irrigation is when drought stress reaches grade 3., D. T. Gao, C. Y. Shi, Q. L. Li, Z. F. Wei, L. Liu, J. R. Feng., and Obsahuje bibliografické odkazy
At a three-leaf stage, two Fe treatments [0 mg kg-1 (Fe-) and 20 mg.kg-1 (Fe+) in the form of FeCl3] were used in the soil of the pot and then two concentrations of α-ketoglutaric acid [0 mg L-1 (A-) and 50 mg L-1 (A+)] were sprayed to the rice plants of Meixiangzhan and Yuxiangyouzhan cultivars. We showed that seedlings exhibited an increased length and fresh and dry mass of shoots and roots with treatments Fe+A- and Fe-A+, as well as the Fe content increased greatly. Both treatments increased the morphological characteristic values of roots and promoted photosynthesis. Interestingly, Fe+A+ notably affected the photosynthesis of fragrant rice seedlings; however, it exerted no significant differences on other parameters. Overall, Fe and α-ketoglutaric acid had the potential for improving the growth of fragrant rice seedlings. The interaction between Fe and α-ketoglutaric acid regulated photosynthesis in seedling leaves, which provided evidence for further improvement of rice cultivation.
The effects of different light-emitting diode (LED) lights on saffron growth and photosynthetic characteristic were explored. Physiological mechanisms were explained by chlorophyll a fluorescence transient curves (OJIP) and JIP-test parameters. A decrease in the red to blue light ratio resulted in negative effects, particularly for monochromatic blue (B) LED light; saffron seedlings showed reduced chlorophyll accumulation, inhibited leaf elongation, and decreased photosynthetic performance. In the OJIP curve, the higher positive K-band observed for B LED light indicated that oxygen-evolving complex activation significantly decreased. B LED light inhibited the electron transport between primary quinone acceptor and secondary quinone acceptor as well as the existence of reducing plastoquinone centers, and increased energy dissipation of reaction centers. Otherwise, the red to blue light ratio of 2:1 had a positive effect on saffron cultivation, resulting in the longest leaf lengths, highest chlorophyll content, and photosynthetic characteristics. This study provides theoretical guidance for saffron agricultural practices.
Anticipating warming related to climate change, commercial mango plantations in China have been shifting from lower to higher elevations. Such a practice may expose mangoes to climatic conditions that could affect photosynthesis. Photosynthesis research on mango has previously examined mature plantations but exploring adequate functions before the time of fruit production is necessary for later crop success. Therefore, we established two main commercial mango cultivars, Tainong No. 1 and Jinhuang, at 450 m and 1,050 m and examined their photosynthetic performance. Our results showed that photosynthetic capacity parameters, including maximum photosynthetic rate, apparent quantum yield, maximum carboxylation rate, and photosynthetic electron transport rate, were significantly different between cultivars due to elevation and positively correlated with leaf nitrogen per area. Moreover, the seasonal gas exchange of the two cultivars showed variations due to elevation, particularly during the warmer seasons. Therefore, elevation affects the photosynthetic performance of these mango cultivars.
Alkaline stress is important abiotic stress that restricts the growth and physiological activity of sorghum (Sorghum bicolor L. Moench). We aimed to investigate the effects of alkaline stress on alkali-tolerant SX44B and alkali-sensitive 262B sorghum inbred lines. The results showed that alkaline stress decreased the content of chlorophyll, activity of photosystem II, net photosynthetic rate, and destroyed chloroplast morphology. These changes were less pronounced in SX44B, possibly owing to its higher antioxidant enzyme activity and nonphotochemical quenching. Alkaline stress decreased water content, transpiration rate, and stomatal conductance while increasing the leaf temperature, with the effect being more pronounced in 262B. A significant correlation was observed between leaf-air temperature difference (ΔT) and relative water content and gas-exchange parameters, especially in 262B. Therefore, ΔT is an effective indicator for monitoring changes in sorghum leaves under alkaline stress and evaluating the alkali tolerance of different sorghum germplasm.