We provide here a general introduction on chlorophyll (Chl) a fluorescence, then we present our measurements on fast (< 1 s) induction curves (the so-called OJIP transients) on dark-adapted intact leaves of Arabidopsis thaliana, under five different light intensities [in the range of ~ 500 to ~ 3,000 µmol(photons) m‒2 s‒1] using two different instruments: Handy PEA (Hansatech Instruments, UK; excitation light, 650 nm) and FluorPen (model FP-110; Photon Systems Instruments, The Czech Republic; excitation light, 470 nm). We then discuss the observed differences in the OJIP curves, as well as in Fo (F20μs, F50μs, or the extrapolated Ft→0), FP (the peak), and the ratios FP/Fo, and Fv (= FP ‒ Fo)/FP in terms of differences in excitation light intensity and absorptance (or absorbance) of the excitation light by the leaves, and other factors, as well as the data available in the literature. We suggest that such measurements be accompanied, in the future, by parallel measurements on Chl a fluorescence imaging, an area pioneered by Hartmut K. Lichtenthaler., B. Padhi, G. Chauhan, D. Kandoi, A. Stirbet, B. C. Tripathy, G. Govindjee., and Obsahuje bibliografické odkazy
In stressful environments, invasive plants acclimate more efficiently than native plants and hybridization mainly contributes to this process. We examined changes in the morphological characteristics, photosynthetic characteristics, and antioxidant capacity of Sphagneticola trilobata and its hybrids in a low-light environment to explore their invasiveness, with Sphagneticola calendulacea serving as the control. The morphological plasticity of S. trilobata was not dominant, the maximal photochemical efficiency of PSII, actual quantum yield of PSII, and electron transport rate of PSⅡ increased and nonphotochemical quenching decreased, while S. calendulacea and the hybrid produced opposite results. S. trilobata showed fewer spots stained for reactive oxygen species in tissues, with an increase in superoxide dismutase activity. Although S. trilobata is a heliophilous plant, we found that the shade tolerance of S. trilobata and the hybrid were stronger than that of S. calendulacea, which may be one important mechanism of invasion.
Active control of photosynthetic activities is important in plant physiological study. Although models of plant photosynthesis have been built at different scales, they have not been fully examined for their application in plant growth control. However, we do not have an infrastructure to support such experiments since current plant growth chambers usually use fixed control protocols. In our current paper, an open IoT-based framework is proposed. This framework allows a plant scientist or agricultural engineer, through an application programming interface (API), in a desirable programming language, (1) to gather environmental data and plant physiological responses; (2) to program and execute control algorithms based on their models, and then (3) to implement real-time commands to control environmental factors. A plant growth chamber was developed to demonstrate the concept of the proposed open framework.
Shade treatment was applied to tall fescue with 30% full light. The results showed that shade increased chlorophyll (Chl) content per unit leaf mass, decreased the Chl a/b ratio in the mature leaves, and decreased effective quantum yield based on Chl fluorescence compared to the full light treatment. Shade stress did not cause increased contents of malondiadehyde at the early stages of leaf development. However, normalized vegetation indices were able to detect shade stress. Chloroplasts in the shaded leaves are arranged tightly against the periclinal cell wall and are in a spindle shape. There were no differences in the number of grana per chloroplast or grana size (thylakoids per granum) between shade and full light treatment. In conclusion, tall fescue leaves showed unique ultrastructure changes. Turfgrass managers could use vegetation indices developed from the leaf light reflection spectrum as an effective tool to assess shade stress levels and make management decisions.
Mesembryanthemum crystallinum is an annual succulent plant that is being used as an emerging healthy leafy vegetable. To investigate the growth and physiological response of M. crystallinum to artificial lighting, five different light treatments were applied at 150 µmol(photon) m-2 s-1, which were white (W), different rations of red/blue (B) (15, 40, and 70%B), and blue (100%B), respectively. Our results showed that plants could gain as much as edible leaf area and dry mass with a certain ratio of blue (40%) in comparison with W. Plants grown under 100%B resulted in reduced photosynthetic rate, leaf area, and fresh mass compared with W. Adding blue fraction in the light regime enhanced the photosynthetic performance by influencing the amount of chlorophyll (Chl), Chl a/b, and specific leaf area. Under red/blue treatments, the electron transport rate and effective quantum yield of both PSII and PSI increased, while the nitrate content was reduced and flavonoids and total antioxidant capacity were unaffected.
Chlorophyll fluorescence has developed into a well-established noninvasive technique to study photosynthesis and by extension, the physiology of plants and algae. The versatility of the fluorescence analysis has been improved significantly due to advancements in the technology of light sources, detectors, and data handling. This allowed the development of an instrumention that is effective, easy to handle, and affordable. Several of these techniques rely on point measurements. However, the response of plants to environmental stresses is heterogeneous, both spatially and temporally. Beside the nonimaging systems, low- and high-resolution imaging systems have been developed and are in use as real-time, multi-channel fluorometers to investigate heterogeneous patterns of photosynthetic performance of leaves and algae. This review will revise in several paragraphs the current status of chlorophyll fluorescence imaging, in exploring photosynthetic features to evaluate the physiological response of plant organisms in different domains. In the conclusion paragraph, an attempt will be made to answer the question posed in the title., R. Valcke., and Obsahuje bibliografické odkazy
Chlorophyll a fluorescence analysis (CFA) has been accepted to study postharvest activity and stability of photosynthesis of vegetables and salad greens, and some fruits. Commercial chlorophyll fluorescence imaging (CFI) systems may provide additional insight into spatial and temporal dynamics of photosynthesis. This yields valuable information on the effects of postharvest handling and processing (sorting, cutting, packaging, etc.) on physiological activity and 'internal quality' of green produce, and its changes. Here, meaning and physiological basics of relevant fluorescence parameters is briefly summarised, while major focus is on recent applications of CFI to evaluate quality and quality maintenance during postharvest handling and minimal processing of fresh fruits and vegetables. CFI is given surprisingly little attention in the monitoring of postharvest quality, although it is suitable for adjusting and/or optimising innovative postharvest techniques. Knowledge of the physiological base and the limit of interpretation is indispensable for meaningful interpretations of results to draw correct consequences., W. B. Herppich., and Obsahuje bibliografické odkazy
Our research aimed to study the correlation between the SPAD-502 readings and the color space CIE L*a*b* values in two cultivars of Alstroemeria sp. during leaf senescence and to evaluate the statistical criteria used in the selection of the best fit calibration functions. We demonstrate the importance of the Akaike information criterion and the parsimonious function besides the coefficient of determination. The reliability of the functions was tested by Student's t-test comparison between the chlorophyll (Chl) estimated from SPAD readings and their chemical concentrations. Polynomial and Hoerl function described well the changes in Chl a and total Chl (a+b) during senescence, but calibration functions are required to perform for each cultivar. We demonstrated that CIE L*a*b* system is reliable to estimate SPAD reading at stages of leaf senescence of Alstroemeria sp. and can be used instead of SPAD-502.
Little data on the role played in vivo by chloroplast protein AtDeg2 as a chaperone is available. Therefore, we sought for chloroplast proteins protected from high irradiance-induced interprotein aggregation via disulphide bridges by AtDeg2 acting as a holdase. To reach this goal, we performed analyses which involved comparative diagonal electrophoreses of lysates of chloroplasts isolated from wild type (WT) plants and transgenic plants 35S:AtDEG2ΔPDZ1-GFP which expressed AtDeg2 lacking its chaperone activity but retaining the protease activity. The results of the analyses indicate that AtDeg2 acting as a holdase prevents a single chloroplast protein, i.e., the γ1 subunit of ATP synthase from long-term high irradiance-induced homodimerization mediated by disuplhide bridges and this allows us to better understand a complexity of physiological significance of AtDeg2 - the chloroplast protein of dual protease/chaperone activity.
The content of chlorophylls (Chl) (a+b), total carotenoids (x+c), and the pigment ratios of Chl a/b and Chls to carotenoids (a+b)/(x+c) of green leaves of five C4 plants were determined and compared to those of C3 plants. The C4 plants were: Pacific and Chinese silvergrass (Miscanthus floridulus and Miscanthus sinensis), sugar cane (Saccharum officinarum) as well as feed and sugar maize (Zea mays). The three C3 plants were beech, ginkgo, and oak. C4 plants possess higher values for the ratio Chl a/b (3.4-4.5) as compared to the C3 plants (2.6-3.3). Sugar maize had the highest values for Chl a/b (4.04-4.70) and exceptionally high contents of total carotenoids and consequently lower values for the ratio of (a+b)/(x+c) (mean: 3.75 ± 0.6). During autumnal senescence also C4 plants showed a faster decline of Chl b as compared to Chl a yielding high values for Chl a/b of 6 to 8. Chlorophylls declined faster than carotenoids yielding low (a+b)/(x+c) values below 1.0.