A flash-lamp chlorophyll (Chl) fluorescence imaging system (FL-FIS) is described that allows to screen and image the photosynthetic activity of several thousand leaf points (pixels) of intact leaves in a non-destructive way within a few seconds. This includes also the registration of several thousand leaf point images of the four natural fluorescence bands of plants in the blue (440 nm) and green (520 nm) regions as well as the red (near 690 nm) and far-red (near 740 nm) Chl fluorescence. The latest components of this Karlsruhe FL-FIS are presented as well as its advantage as compared to the classical single leaf point measurements where only the fluorescence information of one leaf point is sensed per each measurement. Moreover, using the conventional He-Ne-laser induced two-wavelengths Chl fluorometer LITWaF, we demonstrated that the photosynthetic activity of leaves can be determined measuring the Chl fluorescence decrease ratio, RFd (defined as Chl fluorescence decrease Fd from maximum to steady state fluorescence Fs:Fd/Fs), that is determined by the Chl fluorescence induction kinetics (Kautsky effect). The height of the values of the Chl fluorescence decrease ratio RFd is linearly correlated to the net photosynthetic CO2 fixation rate PN as is indicated here for sun and shade leaves of various trees that considerably differ in their PN. Imaging the RFd-ratio of intact leaves permitted the detection of considerable gradients in photosynthetic capacity across the leaf area as well as the spatial heterogeneity and patchiness of photosynthetic quantum conversion within the control leaf and the stressed plants. The higher photosynthetic capacity of sun versus shade leaves was screened by Chl fluorescence imaging. Profile analysis of fluoresence signals (along a line across the leaf area) and histograms (the signal frequency distribution of the fluorescence information of all measured leaf pixels) of Chl fluorescence yield and Chl fluorescence ratios allow, with a high statistical significance, the quantification of the differences in photosynthetic activity between various areas of the leaf as well as between control leaves and water stressed leaves. The progressive uptake and transfer of the herbicide diuron via the petiole into the leaf of an intact plant and the concomitant loss of photosynthetic quantum conversion was followed with high precision by imaging the increase of the red Chl fluorescence F690. Differences in the availability and absorption of soil nitrogen of crop plants can be documented via this flash-lamp fluorescence imaging technique by imaging the blue/red ratio image F440/F690, whereas differences in Chl content are detected, by collecting images of the fluorescence ratio red/far-red, F690/F740., and H. K. Lichtenthaler ... [et al.].
Greenhouse-grown susceptible 20-d-old seedlings of Theobroma cacao genotypes Catongo and tolerant genotype SCA6xCatongo were inoculated with a mixture of isolates of Crinipellis perniciosa, the causal agent of witches' broom. The characteristics of chlorophyll a fluorescence emission were monitored during leaf ontogeny using a portable system PAM-2000. In both inoculated and non-inoculated genotypes, significant differences were found for the effective quantum yield values of photosystem (PS) 2 (ΔF/Fm') at the B (7 to 14-d-old), D (21 to 30-d-old), and E (>30-d-old) stages of leaf development, and in quantum yield of the non-cyclic photosynthetic electron transport between PS2 and PS1 [qp(Fv/Fm)] and quencher efficiency [(Fm-Ft)/F0] at the B, C (15 to 20-d-old) and D stages. Intergenotypic differences were found only for the [qp(Fv/Fm)] and [(Fm-Ft)/F0] values at the E stage, and for fluorescence quenching (Fm-Ft) at the B and E stages. Highly significant inter- and intragenotype relationships were found between the rate of photosynthetic electron transport to PS2 (Amax) and maximum fluorescence during actinic irradiation (Fm'). Also, each of the highly significant relationships between (Fm-Ft) and Amax, [(Fm-Ft)/F0] and ΔF/Fm', and between [(Fm-Ft)/F0] and Amax were represented by a general model, independent of treatments. Therefore, alterations in energy distribution in the radiant energy collector complex interior of PS2 and reduction in absorption of photosynthetically active radiation were observed in the infected plants, mainly in the hybrid at the C stage. Also, variations were found in the noncyclic photosynthetic electron transport at the B and C stages in the infected Catongo. and I. C. F. Santos, A.-A. F. de Almeida, R. R. Valle.
Chlorophyll fluorescence parameters (Chl FPs) derived from the slow (long-term) induction kinetics of modulated Chl a fluorescence are reviewed and analysed with respect to their application in photosynthesis research. Only four mutually independent Chl FPs, calculated from values of five essential Chl fluorescence (ChlF) yields, are distinguished as the basic ones. These are: the maximum quantum yield of PS2 photochemistry (ΦPO), the photochemical quenching of variable ChlF (qP), the non-photochemical quenching of variable ChlF (qN), and the relative change of minimum ChlF (qO). ΦPO refers to the dark-adapted state of a thylakoid membrane, qP, qN and qO characterise the light-adapted state. It is demonstrated that all other Chl FPs can be determined using this quartet of parameters. Moreover, three FPs related to the non-radiative energy dissipation within thylakoid membranes are evaluated, namely: the non-photochemical ChlF quenching (NPQ), the complete non-photochemical quenching of ChlF (qCN), and the effective quantum yield of non-photochemical processes in PS2 (ΦN). New FPs, the total quenching of variable ChlF (qTV) and the absolute quenching of ChlF (qA) which allow to quantify co-action of the photochemical and non-photochemical processes during a light period are defined and analysed. The interpretation of Chl FPs and recommendations for their application in the photosynthesis research are also given. Some alternative FPs used in the laboratory practice have only an approximate character and can lead to incorrect conclusions if applied to stressed plants. They are reviewed and compared with the standard ones. All formulae and conclusions discussed herein are verified using experimental values obtained on young seedlings of the Norway spruce (Picea abies [L.] Karst.).
One-year old sweet almond (Prunus dulcis) seedlings were submitted to four levels of salt stress induced by NaCl, namely 0.3, 0.5, 0.7, and 1.0 S m-1. Effects of salt stress on a range of chlorophyll (Chl) fluorescence parameters (Chl FPs) and Chl contents were investigated in order to establish an eco-physiological characterization of P. dulcis to salinity. Salt stress promoted an increase in F0, Fs, and F0/Fm and a decrease in Fm, F'm, Fv/Fm, qP, ΔF/F'm, Fv/F0, and UQF(rel), in almost all Chl fluorescence yields (FY) and FPs due to its adverse effect on activity of photosystem 2. No significant changes were observed for quenchings qN, NPQ, and qN(rel). The contents of Chl a and b and their ratio were also significantly reduced at increased salt stress. In general, adverse salinity effects became significant when the electric conductivity of the nutrient solution (ECn) exceeded 0.3 S m-1. The most sensitive salt stress indicators were Fv/F0 and Chl a content, and they are thus best used for early salt detection in P. dulcis. Monitoring of a simple Chl FY, such as F0, also gave a good indication of induced salt stress due to the significant correlations observed between the different Chl FYs and FPs. Even essential Chl FYs, like F0, Fm, F'm, and Fs, and mutually independent Chl FPs, like Fv/F0 and qP, were strongly correlated with each other. and A. Ranjbarfordoei, R. Samson, P. Van Damme.
The objective of this study was to use nondestructive measurements as the precise irrigation indices for potted star cluster (Pentas lanceolata). Drought stress was imposed on plants for 0, 3, 5, 7, 12, and 16 d by withholding water. Measurements were conducted on the third leaf counted from the apex (upper leaves) and on the third leaf from the bottom (lower leaves). Within the range of soil water content (SWC) from 10 to 45%, leaf water potential (WP), SWC, and soil matric potential (SMP), chlorophyll fluorescence, photochemical reflectance index (PRI), adjusted normalized difference vegetation index (aNDVI), and the reflectance (R) at 1950 nm (R1950) were measured. The plants reached the temporary wilting point at -3.87 MPa of leaf WP; the maximal fluorescence yield of the light-adapted state (Fm′) ratio of upper-to-lower leaves was 1.7. When the Fm′ ratio was 1.3, it corresponded to lower-leaf WP < -2.27 MPa, SWC < 21%, SMP < -20 kPa, PRI < 0.0443, aNDVI < 0.0301, and R1950 > 8.904; it was the time to irrigate. In conclusion, the Fm′ ratio of upper-to-lower leaves was shown to be a nondestructive predictor of leaf WP and can be used to estimate irrigation timing., C. W. Wu, M. C. Lee, Y. L. Peng, T. Y. Chou, K. H. Lin, Y. S. Chang., and Obsahuje seznam literatury
We examined effects of late-season heat stress (L-SHS) on chlorophyll (Chl) fluorescence parameters and yield of bread wheat as well as roles of phosphate bio-fertilizer (PB-F) and Zn and B to compensate for the likely effects of heat stress. Factors were planting date (21 November and 5 January to coincide with grain filling to L-SHS) as the main factor, no inoculation (control) and inoculation of the seeds with PB-F as the sub-factor, and foliar application of water (control), Zn, B, and Zn + B as 3 L ha-1 as
sub-sub factor. Results revealed that L-SHS reduced maximal quantum yield of PSII photochemistry, effective quantum yield of PSII photochemistry, efficiency of PSII in the light-adapted state, and the grain yield. Moreover, L-SHS increased the nonphotochemical quenching. The PB-F mitigated the effects of L-SHS on Chl fluorescence, yield, and yield components. Among nutrients, the combined Zn + B was more effective in reducing the effects of L-SHS than that of Zn and B alone. Nevertheless, there was an interaction between foliar nutrients application and PB-F, suggesting that Zn application alone had a profound influence on improving Chl fluorescence parameters and increased yield in combination with PB-F., H. R. Eisvand, H. Kamaei, F. Nazarian., and Obsahuje bibliografii
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.
A field experiment was conducted with two cassava cultivars and eight levels of nitrogen to examine the relationship between extractable chlorophyll (Chl) content of cassava leaves and both the Chl meter value (SPAD) and leaf colour chart (LCC) score. The SPAD, LCC, and Chl a+b content were influenced by leaf position, growth stage, cultivar (cv.), and N fertilization. The cvs. and N fertilization had significant effect on SPAD, LCC, and Chl a+b content of youngest fully expanded leaf (leaf 1) blade in most cases. An F-test indicated that common equations pooled across cvs., N fertilization, and growth stages could be used to describe the relationships between Chl a+b content and LCC and between SPAD and LCC, but not between SPAD and Chl a+b content. Relationships between tuber yield and SPAD, LCC, and Chl a+b content were significant (p<0.05) and positive at 30 and 60 d after planting. Thus LCC and SPAD can be used to estimate leaf Chl content which is an indicator of leaf N status. and M. Haripriya Anand, G. Byju.
Photosynthetic pigment contents of the second sexual generation of a cybrid plant (C-18-1) resulting from Solanum nigrum genome and Solanum tuberosum plastome were compared to those of the original (S. nigrum). Chloroplast ultrastructure alterations among S. tuberosum, cybrid, and S. nigrum were also studied. Leaf segments of both the cybrid and S. nigrum plants were cultured on shoot induction medium [B5 supplemented with 0.56 g m-3 benzylaminopurine (BAP)] for one week in light, to induce adventitious bud formation. These leaf segments were then placed in darkness for 5 weeks to form a white shoot. The respective cybrid plant had the same phenotype of the fusion recipient plant (S. nigrum) and was fertile. The rate of photosynthetic pigment biosynthesis in the white cybrid shoots was lower than that of the original plant shoots after subjecting the two plants to the same conditions of different irradiation periods (0, 2, 4, 6, 8, and 10 d). At the 10-d irradiation period of two white shoot plants, the total pigment content of S. nigrum shoot increased approximately 3-fold over that of the cybrid shoot. Numbers of grana and thylakoids as well as chloroplast size were decreased in cybrid cells in comparison to those in S. tuberosum cells. Under atrazine stress, while the chloroplast ultrastructure of the cybrid cells (atrazine sensitive) was strongly influenced, the chloroplasts of S. nigrum (atrazine resistant) were not affected. and K. A. Fayez, A. M. Hassanein.
Chlorophyll (Chl) α fluorescence induction (transient), measured by exposing dark-adapted samples to high light, shows a polyphasic rise, which has been the subject of extensive research over several decades. Several Chl fluorescence parameters based on this transient have been defined, the most widely used being the FV [= (FM-F0)]/FM ratio as a proxy for the maximum quantum yield of PSII photochemistry. However, considerable additional information may be derived from analysis of the shape of the fluorescence transient. In fact, several performance indices (PIs) have been defined, which are suggested to provide information on the structure and function of PSII, as well as on the efficiencies of specific electron transport reactions in the thylakoid membrane. Further, these PIs have been proposed to quantify plant tolerance to stress, such as by high light, drought, high (or low) temperature, or N-deficiency. This is an interesting idea, since the speed of the Chl α fluorescence transient measurement (<1 s) is very suitable for high-throughput phenotyping. In this review, we describe how PIs have been used in the assessment of photosynthetic tolerance to various abiotic stress factors. We synthesize these findings and draw conclusions on the suitability of several PIs in assessing stress responses. Finally, we highlight an alternative method to extract information from fluorescence transients, the Integrated Biomarker Response. This method has been developed to define multi-parametric indices in other scientific fields (e.g., ecology), and may be used to combine Chl α fluorescence data with other proxies characterizing CO2 assimilation, or even growth or grain yield, allowing a more holistic assessment of plant performance., A. Stirbet, D. Lazár, J. Kromdijk, Govindjee., and Obsahuje bibliografické odkazy