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Fluorescence Parameters (fluorescence + parameter)
Kinds of Fluorescence Parameters Selected AbstractsXanthophyll Cycle and Inactivation of Photosystem II Reaction Centers Alleviating Reducing Pressure to Photosystem I in Morning Glory Leaves under Short-term High IrradianceJOURNAL OF INTEGRATIVE PLANT BIOLOGY, Issue 7 2007Xin-Guo Li Abstract Under 30-min high irradiance (1500 ,mol m,2 s,1), the roles of the xanthophyll cycle and D1 protein turnover were investigated through chlorophyll fluorescence parameters in morning glory (Ipomoea setosa) leaves, which were dipped into water, dithiothreitol (DTT) and lincomycin (LM), respectively. During the stress, both the xanthophyll cycle and D1 protein turnover could protect PSI from photoinhibition. In DTT leaves, non-photochemical quenching (NPQ) was inhibited greatly and the oxidation level of P700 (P700+) was the lowest one. However, the maximal photochemical efficiency of PSII (Fv/Fm) in DTT leaves was higher than that of LM leaves and was lower than that of control leaves. These results suggested that PSI was more sensitive to the loss of the xanthophyll cycle than PSII under high irradiance. In LM leaves, NPQ was partly inhibited, Fv/Fm was the lowest one among three treatments under high irradiance and P700+ was at a similar level as that of control leaves. These results implied that inactivation of PSII reaction centers could protect PSI from further photoinhibition. Additionally, the lowest of the number of active reaction centers to one inactive reaction center for a PSII cross-section (RC/CSo), maximal trapping rate in a PSII cross-section (TRo/CSo), electron transport in a PSII cross-section (ETo/CSo) and the highest of 1-qP in LM leaves further indicated that severe photoinhibition of PSII in LM leaves was mainly induced by inactivation of PSII reaction centers, which limited electrons transporting to PSI. However, relative to the LM leaves the higher level of RC/CSo, TRo/CSo, Fv/Fm and the lower level of 1-qP in DTT leaves indicated that PSI photoinhibition was mainly induced by the electron accumulation at the PSI acceptor side, which induced the decrease of P700+ under high irradiance. [source] Does the source of nitrogen affect the response of subterranean clover to prolonged root hypoxia?JOURNAL OF PLANT NUTRITION AND SOIL SCIENCE, Issue 2 2010Faouzi Horchani Abstract Nitrogen (N) is taken up by most plant species in the form of nitrate (NO) or ammonium (NH). The plant response to continuous ammonium nutrition is species-dependent. In this study, the effects of the source of N nutrition (NO, NH, or the mixture of NO and NH) on the response of clover (Trifolium subterraneum L. cv. 45C) plants to prolonged root hypoxia was studied. Under aerobic conditions, plant growth was strongly depressed by NH, compared to NO or mixed N nutrition, as indicated by the significant decrease in root and shoot-dry-matter production (DW), root and shoot water contents (WC), leaf chlorophyll concentration, and chlorophyll fluorescence parameters (F0, Fv/Fm). However, the N source had no effect on chlorophyll a,to,chlorophyll b ratio. Under hypoxic conditions, the negative effects of root hypoxia on plant-growth parameters (DW and WC), leaf chlorophyll concentration, and chlorophyll fluorescence parameters were alleviated by NH rather than NO supply. Concomitantly, shoot DW,to,root DW ratio, and root and leaf NH concentrations were significantly decreased, whereas root and leaf carbohydrate concentrations, glutamine synthetase activities, and protein concentrations were remarkably increased. The present data reveal that the N source (NO or NH) is a major factor affecting clover responses to hypoxic stress, with plants being more tolerant when NH is the N form used. The different sensitivity is discussed in terms of a competition for energy between nitrogen assimilation and plant growth. [source] Chlorophyll content and fluorescence responses cannot be used to gauge reliably phytoplankton biomass, nutrient status or growth rateNEW PHYTOLOGIST, Issue 3 2006Mikaela Kruskopf Summary ,,To consider the relationship between chlorophyll a (Chl a) content and phytoplankton growth and nutrient status, four phytoplankton species were grown in nitrogen (N)-limited [and, for one species, phosphorus (P)-limited] culture and measurements were made of CNP biomass, in vivo and in vitro Chl a content, the ratio of variable to maximum fluorescence (FV/FM) and the performance index for photosynthesis, PIABS (a derivative of the O-J-I-P analysis of photosystem II functionality). ,,Interspecies differences plus the development of intraspecies differences during nutrient stress produced c. 10-fold variations in Chl : C. Estimates of C from in vivo Chl content were better than those from extracted Chl content, as the decline in Chl : C during nutrient stress was offset in part by increased Chl fluorescence. ,,FV/FM was not a robust indicator of nutrient status or relative growth rate. Responses of FV/FM in cells re-fed the limiting nutrient showed no consistent pattern with which to gauge nutrient status. PIABS showed some promise as an indicator of nutrient status and relative growth rate. ,,Chl a content and fluorescence parameters do not deserve the unquestioned status they usually enjoy as indicators of biomass and physiological status. [source] Tryptophan Fluorescence in the Bacillus subtilis Phototropin-related Protein YtvA as a Marker of Interdomain Interaction,PHOTOCHEMISTRY & PHOTOBIOLOGY, Issue 1 2004Aba Losi ABSTRACT The Bacillus subtilis protein YtvA, related to plant phototropins (phot), binds flavin mononucleotide (FMN) within the N-terminal light, oxygen and voltage (LOV) domain. The blue light-triggered photocycle of YtvA and phot involves the reversible formation of a covalent photoadduct between FMN and a cysteine (cys) residue. YtvA contains a single tryptophan, W103, localized on the LOV domain and conserved in all phot-LOV domains. In this study, we show that the fluorescence parameters of W103 in YtvA-LOV are markedly different from those observed in the full-length YtvA. The fluorescence quantum yields are ca 0.03 and 0.08, respectively. In YtvA-LOV, the maximum is redshifted (ca 345 vs 335 nm) and the average fluorescence lifetime shorter (2.7 vs 4.7 ns). These data indicate that W103 is located in a site of tight contact between the two domains of YtvA. In the FMN-cys adduct, selective excitation of W103 at 295 nm results in minimal changes of the fluorescence parameters with respect to the dark state. On 280 nm excitation, however, there is a detectable decrease in the fluorescence emitted from tyrosines, with concomitant increase in W103 fluorescence. This effect is reversible in the dark and might arise from a light-regulated energy transfer process from a yet unidentified tyrosine to W103. [source] The Effect of Decreasing Temperature up to Chilling Values on the in vivo F685/F735 Chlorophyll Fluorescence Ratio in Phaseolus vulgaris and Pisum sativum: The Role of the Photosystem I Contribution to the 735 nm Fluorescence Band ,PHOTOCHEMISTRY & PHOTOBIOLOGY, Issue 1 2000Giovanni Agati ABSTRACT The effect of leaf temperature (T), between 23 and 4°C, on the chlorophyll (Chl) fluorescence spectral shape was investigated under moderate (200 ,E m,2 s,1) and low (30,35 ,E m,2 s,1) light intensities in Phaseolus vulgaris and Pisum sativum. With decreasing temperature, an increase in the fluorescence yield at both 685 and 735 nm was observed. A marked change occurred at the longer emission band resulting in a decrease in the Chl fluorescence ratio, F685/F735, with reducing T. Our fluorescence analysis suggests that this effect is due to a temperature-induced state 1,state 2 transition that decreases and increases photosystem II (PSII) and photosystem I (PSI) fluorescence, respectively. Time-resolved fluorescence lifetime measurements support this interpretation. At a critical temperature (about 6°C) and low light intensity a sudden decrease in fluorescence intensity was observed, with a larger effect at 685 than at 735 nm. This is probably linked to a modification of the thylakoid membranes, induced by chilling temperatures, which can alter the spillover from PSII to PSI. The contribution of photosystem I to the long-wavelength Chl fluorescence band (735 nm) at room temperature was estimated by both time-resolved fluorescence lifetime and fluorescence yield measurements at 685 and 735 nm. We found that PSI contributes to the 735 nm fluorescence for about 40, 10 and 35% at the minimal (F0), maximal (Fm) and steady-state (Fs) levels, respectively. Therefore, PSI must be taken into account in the analysis of Chl fluorescence parameters that include the 735 nm band and to interpret the changes in the Chl fluorescence ratio that can be induced by different agents. [source] Oxygen evolution and respiration of the cyanobacterium Synechocystis sp.PHYSIOLOGIA PLANTARUM, Issue 3 2005PCC 6803 under two different light regimes applying light/dark intervals in the time scale of minutes The photosynthetic performance of the cyanobacterium Synechocystis sp. PCC 6803 exposed to intermittent light was studied by measuring oxygen evolution, respiration and the fluorescence parameters for maximum efficiency of excitation energy capture by photosystem II (PSII) reaction centres (Fv/Fm), PSII quantum yield (,F/Fm1) and non-photochemical quenching (NPQ). Cultures were pre-acclimated to constant light conditions. Block and sinusoidal light regimes were tested using four photon-flux densities (PFDs) applied in light/dark intervals of 1:1, 5:5 and 10:10 min. Light use was higher under the sinusoidal light regime compared with the block regime. The accumulated gross photosynthesis of the cyanobacterium was lower under intermittent light conditions compared with predictions from the photosynthesis-irradiance curve (PI curve). The respiration rates were similar for all light/dark intervals tested. However, the respiration slightly increased with increasing oxygen production for both block and sinusoidal light regime. NPQ, ,F/Fm, and Fv/Fm depended on the PFD rather than on the duration of the light/dark intervals tested, and there was no detected influence of the two applied light regimes. [source] Evaluation of instant light-response curves of chlorophyll fluorescence parameters obtained with a portable chlorophyll fluorometer on site in the fieldPLANT CELL & ENVIRONMENT, Issue 12 2000U. Rascher ABSTRACT Miniaturized pulse-amplitude modulated photosynthesis yield analysers are primarily designed for measuring effective quantum yield (,F/Fm,) of photosystem II under momentary ambient light conditions in the field. Although this provides important ecophysiological information, it is often necessary to learn more about the potential intrinsic capacities of leaves by measuring light-response curves. Thus, instruments provide light-curve programmes, where light intensities are increased in short intervals and instant light-response curves are recorded within a few minutes. This method can be criticized because photosynthesis will most likely not be in steady state. This technical report shows that with the appropriate precautions instant light curves can nevertheless provide reliable information about cardinal points of photosynthesis. First, the geometry of the light source of the instrument in relation to the quantum sensor must be considered and quantum sensor readings must be corrected. Second, the measurements of the light-response curves must be compared with readings of effective quantum yield of photosystem II under ambient light conditions where photosynthesis is in steady state. This may show that in the critical range of the light curves either both measurements perfectly coincide or are offset against each other by a constant value (examples are given here). In the first case results of light curves can be taken at face values, and in the second case a simple correction can be applied. With these precautions and careful interpretations instant light-response curves can be an enormous advantage in ecophysiological field work. [source] Effect of a nonhost-selective toxin from Alternaria alternata on chloroplast-electron transfer activity in Eupatorium adenophorumPLANT PATHOLOGY, Issue 5 2005S. Chen AAC-toxin, a putative nonhost-selective phytotoxin, was obtained from Alternaria alternata causing a brown leaf spot disease of Crofton weed (Eupatorium adenophorum). The effect of AAC-toxin on the electron transfer reaction of chloroplasts showed that the activity of photosystem II, but not photosystem I, was completely inhibited by the toxin. AAC-toxin affected the following chlorophyll fluorescence parameters: coefficient of photochemical quenching (qP), the half-time value of fluorescence rise, and the O,J,I,P fluorescence induction kinetics curve, but not the ratio values of Fv/Fm (the quantum yield of photosystem II) and the half-time value of fluorescence quenching. It was concluded that the toxin inhibited electron transfer from QA to QB (primary and secondary quinine acceptors of photosystem II) in photosystem II by competing with QB for the binding site in D1 protein on the thylakoid membrane. [source] | ||||||||||