Chromium toxicity is considered as a major problem for agricultural soil that reduced crop productivity by affecting photosynthetic tissues. Exogenous application of melatonin can alleviate the adverse effects of chromium toxicity on plant growth. However, little is known about its effect on thylakoidal protein complexes responsible for conversion of solar energy to biochemical energy. Chlorophyll fluorescence a transients considered one of the best non-invasive and rapid method for the evaluation of photosynthetic (Photosystem II) efficiency of plants and plant health under environmental stress conditions. In the present study, three-week old plants of two canola cultivars AC-Excel and DGL were applied to melatonin (0, 1, 5, 10 μM) when grown under chromium stress (0, 50 and 100 μM) for further two weeks. Chromium stress reduced the growth (fresh and dry weights of shoots and roots) of both canola cultivars and exogenous application of 5 and 10 μM melatonin improved the growth of canola at 50 or 100 μM chromium stress. This improvement was greater in cv DGL than in AC-Excel. Increasing chromium decreased the photosynthetic pigments (chlorophyll a and chlorophyll b ). However, 5 and 10 μM melatonin application improved chlorophyll a at 50 μM chromium stress. Structural stability and efficiency of photosystem II (PSII) measured as performance index (PI ABS ) and ratios of fluorescence (Fv/Fm, Fv/Fo) Fv decreased due to chromium stress. JIP-test parameters showed that chromium stress increased the absorption and trapping fluxes with decrease in electron transport fluxes which caused the damage to reaction centers (RC), detachment of oxygen evolving complex (OEC) from RC or inefficiency of electron transfer from OEC to RC. Such adverse effects were greater in cv AC-Excel. However exogenous application of melatonin improved PI ABS , electron transport per reaction center (ET/RC), reduced variable fluorescence at J step (V J ) reflecting melatonin protected PSII from chromium stress induced damage by protecting OEC. Thus, OJIP fluorescence transients are quite helpful for understanding the intersystem electron transport beyond photosystem II in canola cultivars due to melatonin application under chromium stress. Findings Exogenous application of melatonin alleviated toxic effects of chromium on plant growth of canola by modulating photosynthesis, enhanced photosystem II efficiency and regulation of electron transport flux to protect photo-inhibition of PSII from oxidative damage.

Climate change, food insecurity, water scarcity, and population growth are some of today's world's frightening problems. Drought stress exerts a constant threat to field crops and is often seen as a major constraint on global agricultural productivity; its intensity and frequency are expected to increase in the near future. The present study investigated the effects of drought stress (15% w/v polyethylene glycol PEG-6000) on physiological and biochemical changes in five Brassica napus cultivars (ZD630, ZD622, ZD619, GY605, and ZS11). For drought stress induction, 3-weekold rapeseed oil seedlings were treated with PEG-6000 in full strength Hoagland nutrient solution for 7 days. PEG treatment significantly decreased the plant growth and photosynthetic efficiency, including primary photochemistry (Fv/Fm) of PSII, intercellular CO 2 , net photosynthesis, chlorophyll contents, and water-use efficiency of all studied B. napus cultivars; however, pronounced growth retardations were observed in cultivar GY605. Drought-stressed B. napus cultivars also experienced a sharp rise in H 2 O 2 generation and malondialdehyde (MDA) content. Additionally, the accumulation of ROS was accompanied by increased activity of enzymatic antioxidants (superoxide dismutase, peroxidase, catalase, ascorbate peroxidase, glutathione reductase, and monodehydroascorbate reductase), although the increase was more obvious in ZD622 and ZS11. Drought stress also caused an increased endogenous hormonal biosynthesis (abscisic acid, jasmonic acid, salicylic acid) and accumulation of total soluble proteins and proline content, but the extent varies in B. napus cultivars.These results suggest that B. napus cultivars have an efficient drought stress tolerance mechanism, as shown by improved antioxidant enzyme activities, photosynthetic and hormonal regulation. | INTRODUCTIONWater stress is an increasingly scarce resource that decreases crop production in many parts of the world. Drought stress is one of the most severe abiotic environmental stress factors affecting crop production worldwide (Kour et al., 2020). Rapid anthropogenic climatic changes affect the annual precipitation pattern, leading to severe drought stress in many agricultural areas (Scott et al., 2014). Acquiring drought tolerance in plants probably involves molecular, cellular, physiological, and developmental adjustments enabling plants to adopt an adequate response to maintain optimal growth and development (Bergmann, 2020). In plants, drought stress adaptive strategies have been categorized as (1) drought tolerance via early flowering (Khadka et al., 2020), (2) drought escape via enhanced water uptake and reduced

Background Proline can promote growth of plants by increasing photosynthetic activity under both non-stress and abiotic stress conditions. However, its role in non-stressed conditions is least studied. An experiment was conducted to assess as to whether increase in growth of wheat due to seed priming with proline under non-stress condition was associated with proline-induced changes in photosystem II (PSII) activity. Seeds of four wheat varieties (S-24, Sehar-06, Galaxy-13, and Pasban-90) were primed with different concentrations of proline (0, 5, 15 and 25 mM) for 12 h and allowed to grow under normal conditions. Biomass accumulation and photosynthetic performance, being two most sensitive features/indicators of plant growth, were selected to monitor proline modulated changes. Results Seed priming with proline increased the fresh and dry weights of shoots and roots, and plant height of all four wheat varieties. Maximum increase in growth attributes was observed in all four wheat varieties at 15 mM proline. Maximum growth improvement due to proline was found in var. Galaxy-13, whereas the reverse was true for S-24. Moreover, proline treatment changed the Fo, Fm, Fv/Fo, PIABS, PITot in wheat varieties indicating changes in PSII activity. Proline induced changes in energy fluxes for absorption, trapping, electron transport and heat dissipation per reaction center indicated that var. Galaxy-13 had better ability to process absorbed light energy through photosynthetic machinery. Moreover, lesser PSII efficiency in var. S-24 was due to lower energy flux for electron transport and greater energy flux for heat dissipation. This was further supported by the fact that var. S-24 had disturbance at acceptor side of PSI as reflected by reduction in ΔVIP, probability and energy flux for electron transport at the PSI end electron acceptors. Conclusion Seed priming with proline improved the growth of wheat varieties, which depends on type of variety and concentration of proline applied. Seed priming with proline significantly changed the PSII activity in wheat varieties, however, its translation in growth improvement depends on potential of processing of absorbed light energy by electron acceptors of electron transport chain, particularly those present at PSI end.

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The photosynthetic efficiency in plants is affected by salinity. Focus of this study was to observe the consequences of salinity on the rate of photosynthesis in Moringa (Moringa oleifera L.) plants. Experiment was conducted under field conditions with 3 replicates and data of treated and non-treated plants was collected accordingly. Photosynthetic rate was affected by different levels of salt stress. The change in photosynthetic was attributes were determined by OJIP and light response curve calculations by using Fluor Pen [FP 100-PS (Photon system, Czech Republic)] and DUAL-PAM-100 (Walz, Germany). Salinity stress decreased chlorophyll a fluorescence characteristic. The significant quantity of electron transport (φEo), quantum yield of primary photochemistry (φPo), proficiency per trapped excitation (Ψo) and performance index of photosystem II (PSII). Performance index (PIABS) was also declined with salinity in M. oleifera. Our results showed that electron transport rate and photosynthetic rate were inhibited by salinity in M. oleifera. However, in M. oleifera electron transport pathway of PSII was repressed and found varied in plants which are salt resistant. It was concluded that Y(I), ETR(I), Y(II), ETR(II), and Y(NA) were decreased by increasing salinity while NPQ, Y(ND), Y(NO) and Y(NPQ) increased in plants having resistance to salt stress

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