Cited by 732Photosynthetic Processes and MechanismsPhotochemistry and Electron Transfer StudiesPlant Water Relations and Carbon Dynamics

The DOI matches its Crossref record; 65 of the 67 references it cites were found in a registry or an index.

Chlorophyll Fluorescence Parameters: The Definitions, Photosynthetic Meaning, and Mutual Relationships

Open access

Roháček, K.·2002·Photosynthetica

DOI 10.1023/a:1020125719386

Open this paper in CoChat — free account Open PDF

Abstract

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.).

Integrity signals

Registry

Crossref · 10.1023/a:1020125719386

Cites

65 of 65 references verified0 citation errors · 0 not checkable

Statistics

Recomputing p-values needs the paper’s full text.

Claims the paper makes

We couldn’t retrieve this paper’s full text, so its claims and self-check weren’t run. The registry and citation checks still apply.

Claims other papers make about this one

Each is checked against this paper’s own text: does it say what the citing paper says it does?

Chlorophyll fluorescence—a practical guide
Maxwell, K., & Johnson, G. N. (2000) · Journal of Experimental Botany · doi:10.1093/jexbot/51.345.659 · Cited by 9,347
The relationship between the quantum yield of photosynthetic electron transport and quenching of chlorophyll fluorescence
Genty, B., Briantais, J., & Baker, N. R. (1989) · Biochimica et Biophysica Acta (BBA) - General Subjects · doi:10.1016/s0304-4165(89)80016-9 · Cited by 8,741
Chlorophyll Fluorescence And Photosynthesis: The Basics
Krause, G. H., & Weis, E. (1991) · Annual Review of Plant Physiology and Plant Molecular Biology · doi:10.1146/annurev.pp.42.060191.001525 · Cited by 4,278
Continuous recording of photochemical and non-photochemical chlorophyll fluorescence quenching with a new type of modulation fluorometer
Schreiber, U., Schliwa, U., & Bilger, W. (1986) · Photosynthesis Research · doi:10.1007/bf00024185 · Cited by 2,863
Photon yield of O2 evolution and chlorophyll fluorescence characteristics at 77 K among vascular plants of diverse origins
Bj�rkman, O., & Demmig, B. (1987) · Planta · doi:10.1007/bf00402983 · Cited by 2,514
The use of chlorophyll fluorescence nomenclature in plant stress physiology
van Kooten, O., & Snel, J. F. H. (1990) · Photosynthesis Research · doi:10.1007/bf00033156 · Cited by 2,314
Chlorophyll Fluorescence as a Nonintrusive Indicator for Rapid Assessment of In Vivo Photosynthesis
Schreiber, U., Bilger, W., & Neubauer, C. (1995) · Springer eBooks · doi:10.1007/978-3-642-79354-7_3 · Cited by 1,694
Photosynthesis: from Light to Biosphere
GIORDANO, M., & G., B. (1995) · Springer eBooks · doi:10.1007/978-94-009-0173-5 · Cited by 1,670
Role of the xanthophyll cycle in photoprotection elucidated by measurements of light-induced absorbance changes, fluorescence and photosynthesis in leaves of Hedera canariensis
Bilger, W., & Bj�rkman, O. (1990) · Photosynthesis Research · doi:10.1007/bf00033159 · Cited by 1,547
Ecophysiology of Photosynthesis
Schulze, E., & Caldwell, M. M. (1994) · Springer eBooks · doi:10.1007/978-3-642-79354-7 · Cited by 1,535

Show all 67 references

Research works printed but not linked: 5

Anonymous, 2000, Portable fluorometer PAM-2000 and data acquisition software DA-2000. Handbook of Operation. Ed. 2.-Heinz Walz, Effeltrich 1993
Duysens, 1963, Mechanism of two photochemical reactions in algae as studied by means of fluorescence.-
Kautsky, 1934, Chlorophyllfluoreszenz und Kohlensäureassimilation. I. Das Fluoreszenzverhalten grüner Pflanzen, Biochem. Z, 274, 423
Lichtenthaler, 1984, Development of chloroplasts at high and low light quanta fluence rates.-Isr, J. Bot, 33, 185
Walker, 1987, Fluorescence.-

Items 101–200 of 732

Effect of Low Temperature Stress on Photosynthesis and Allied Traits: A Review
Bhattacharya, A. (2022) · Springer eBooks · doi:10.1007/978-981-16-9037-2_3 · Cited by 62
Effect of arbuscular mycorrhizal inoculation on water status and photosynthesis of Populus cathayana males and females under water stress
Li, Z., Wu, N., Liu, T., Chen, H., & Tang, M. (2015) · Physiologia Plantarum · doi:10.1111/ppl.12336 · Cited by 61
Chlorophyll a fluorescence as a tool for a study of the Potato virus Y effects on photosynthesis of nontransgenic and transgenic Pssu-ipt tobacco
Spoustová, P., Synková, H., Valcke, R., & Čeřovská, N. (2013) · Photosynthetica · doi:10.1007/s11099-013-0023-4 · Cited by 61
Expression of Multiple Resistance Genes Enhances Tolerance to Environmental Stressors in Transgenic Poplar (Populus × euramericana ‘Guariento’)
Su, X., Chu, Y., Li, H., Hou, Y., Zhang, B., Huang, Q., Hu, Z., Huang, R., & Tian, Y. (2011) · PLoS ONE · doi:10.1371/journal.pone.0024614 · Cited by 61
Potato plants ectopically expressing A rabidopsis thaliana CBF 3 exhibit enhanced tolerance to high‐temperature stress
Hai-Ou, D. O. U., XV, K., Meng, Q., Li, G., & Yang, X. (2014) · Plant Cell & Environment · doi:10.1111/pce.12366 · Cited by 61
Effects of abscisic acid or benzyladenine on pigment contents, chlorophyll fluorescence, and chloroplast ultrastructure during water stress and after rehydration
Haisel, D., Pospíšilová, J., Synková, H., Schnablová, R., & Baťková, P. (2006) · Photosynthetica · doi:10.1007/s11099-006-0079-5 · Cited by 61
Uptake of CeO2 Nanoparticles and Its Effect on Growth of Medicago arborea In Vitro Plantlets
Gómez, Á., Pintos, B., Manzanera, J. A., Lobo, M. C., Villalobos, N., & Martín, L. (2014) · Biological Trace Element Research · doi:10.1007/s12011-014-0089-2 · Cited by 60
Combined effects of phosphorus nutrition and elevated carbon dioxide concentration on chlorophyll fluorescence, photosynthesis, and nutrient efficiency of cotton
Singh, S. K., & Reddy, V. R. (2014) · Journal of Plant Nutrition and Soil Science · doi:10.1002/jpln.201400117 · Cited by 60
Effect of irradiance and temperature on the photosynthesis of a cultivated red alga, P yropia tenera (= P orphyra tenera), at the southern limit of distribution in J apan
Watanabe, Y., Nishihara, G. N., Tokunaga, S., & Terada, R. (2014) · Phycological Research · doi:10.1111/pre.12053 · Cited by 59
The wheat mutant DELLA-encoding gene (Rht-B1c) affects plant photosynthetic responses to cadmium stress
Dobrikova, A. G., Yotsova, E. K., Börner, A., Landjeva, S. P., & Apostolova, E. (2017) · Plant Physiology and Biochemistry · doi:10.1016/j.plaphy.2017.02.015 · Cited by 58
The effect of irradiance and temperature on the photosynthesis and growth of a cultivated red alga Kappaphycus alvarezii (Solieriaceae) from Vietnam, based on in situ and in vitro measurements
Terada, R., Vo, T. D., Nishihara, G. N., Keisaku, S., Shimada, S., & Kawaguchi, S. (2015) · Journal of Applied Phycology · doi:10.1007/s10811-015-0557-x · Cited by 57
Nutritional benefit from leaf litter utilization in the pitcher plant Nepenthes ampullaria
Pavlovič, A., Slováková, Ľ., & Šantrůček, J. (2011) · Plant Cell & Environment · doi:10.1111/j.1365-3040.2011.02382.x · Cited by 57
Usnic acid controls the acidity tolerance of lichens
Hauck, M., & Jürgens, S.-R. (2008) · Environmental Pollution · doi:10.1016/j.envpol.2007.12.033 · Cited by 57
Leaf photosynthesis and yield components of mung bean under fully open-air elevated [CO2]
Gao, J., Han, X., Seneweera, S. P., Li, P., Zong, Y., Qi, D. O. N. G., Lin, E., & Hao, X.-Y. (2015) · Journal of Integrative Agriculture · doi:10.1016/s2095-3119(14)60941-2 · Cited by 56
A revised energy partitioning approach to assess the yields of non-photochemical quenching components
Guadagno, C. R., Santo, A. V. D., & D’Ambrosio, N. (2010) · Biochimica et Biophysica Acta (BBA) - Bioenergetics · doi:10.1016/j.bbabio.2010.01.016 · Cited by 56
Ecophysiological and antioxidant traits of Salvia officinalis under ozone stress
Pellegrini, E., Francini, A., Lorenzini, G., & Nali, C. (2015) · Environmental Science and Pollution Research · doi:10.1007/s11356-015-4569-5 · Cited by 56
Simulations show that a small part of variable chlorophyll a fluorescence originates in photosystem I and contributes to overall fluorescence rise
Lazár, D. (2013) · Journal of Theoretical Biology · doi:10.1016/j.jtbi.2013.06.028 · Cited by 56
The different strategies of Pinus sylvestris and Larix sibirica to deal with summer drought in a northern Mongolian forest–steppe ecotone suggest a future superiority of pine in a warming climate
Dulamsuren, C., Hauck, M., Bader, M. K., Oyungerel, S., Osokhjargal, D., Nyambayar, S., & Leuschner, C. (2009) · Canadian Journal of Forest Research · doi:10.1139/x09-156 · Cited by 56
Primary productivity and the coupling of photosynthetic electron transport and carbon fixation in the Arctic Ocean
Schuback, N., Hoppe, C. J. M., Tremblay, J., Maldonado, M. T., & Tortell, P. D. (2017) · Limnology and Oceanography · doi:10.1002/lno.10475 · Cited by 56
Determination of heavy metal tolerance threshold in a bamboo species (Arundinaria pygmaea) as treated with silicon dioxide nanoparticles
Emamverdian, A., Ding, Y., Mokhberdoran, F., Ahmad, Z., & Xie, Y. (2020) · Global Ecology and Conservation · doi:10.1016/j.gecco.2020.e01306 · Cited by 56
Hidden drivers of low-dose pharmaceutical pollutant mixtures revealed by the novel GSA-QHTS screening method
Rodea‐Palomares, I., González-Pleiter, M., Gonzalo, S., Rosal, R., Leganés, F., Sabater, S., Casellas, M., Muñoz‐Carpena, R., & Fernández‐Piñas, F. (2016) · Science Advances · doi:10.1126/sciadv.1601272 · Cited by 55
Effects of cadmium on two wheat cultivars depending on different nitrogen supply
Yotsova, E. K., Dobrikova, A. G., Stefanov, M. A., Misheva, S. P., Bardáčová, M., Matušíková, I., Žideková, L., Blehová, A., & Apostolova, E. (2020) · Plant Physiology and Biochemistry · doi:10.1016/j.plaphy.2020.06.042 · Cited by 55
Effect of 24-Epibrassinolide on Chlorophyll Fluorescence and Photosynthetic CO2 Assimilation in Vicia faba Plants Treated with the Photosynthesis-Inhibiting Herbicide Terbutryn
Piñol, R., & Simón, E. (2009) · Journal of Plant Growth Regulation · doi:10.1007/s00344-008-9077-0 · Cited by 55
eGFP-pHsens as a highly sensitive fluorophore for cellular pH determination by fluorescence lifetime imaging microscopy (FLIM)
Schmitt, F., Thaa, B., Junghans, C., Vitali, M., Veit, M., & Friedrich, T. (2014) · Biochimica et Biophysica Acta (BBA) - Bioenergetics · doi:10.1016/j.bbabio.2014.04.003 · Cited by 54
PSII photochemistry and carboxylation efficiency in Liriodendron tulipifera under ozone exposure
Pellegrini, E., Francini, A., Lorenzini, G., & Nali, C. (2010) · Environmental and Experimental Botany · doi:10.1016/j.envexpbot.2010.09.012 · Cited by 54
Using Phenomic Analysis of Photosynthetic Function for Abiotic Stress Response Gene Discovery
Rungrat, T., Awlia, M., Brown, T. B., Cheng, R., Sirault, X. R. R., Fajkus, J., Trtílek, M., Furbank, B., Badger, M. R., Tester, M. A., et al. (2016) · The Arabidopsis Book · doi:10.1199/tab.0185 · Cited by 54
In situ response of Nostoc commune s.l. colonies to desiccation in Central Svalbard, Norwegian High Arctic.
Kvíderová, J., Elster, J., & imek, M. (2011) · Fottea · doi:10.5507/fot.2011.009 · Cited by 53
Chlorophyll Fluorescence Imaging-Based Duckweed Phenotyping to Assess Acute Phytotoxic Effects
Oláh, V., Hepp, A., Irfan, M., & Mészáros, I. (2021) · Plants · doi:10.3390/plants10122763 · Cited by 53
Drought stress, rain and recovery of the intertidal seaweed Fucus spiralis
Schagerl, M., & Möstl, M. (2011) · Marine Biology · doi:10.1007/s00227-011-1748-x · Cited by 53
Estimation of the Relative Sizes of Rate Constants for Chlorophyll De-excitation Processes Through Comparison of Inverse Fluorescence Intensities
Kasajima, I., Takahara, K., Kawai‐Yamada, M., & Uchimiya, H. (2009) · Plant and Cell Physiology · doi:10.1093/pcp/pcp102 · Cited by 53
Leaf Gas Exchange and ChlorophyllaFluorescence in Maize Leaves Infected withStenocarpella macrospora
Bermúdez-Cardona, M. B., Filho, J. A. W., & Rodrigues, F. Á. (2014) · Phytopathology · doi:10.1094/phyto-04-14-0096-r · Cited by 52
Effect of herbicide clomazone on photosynthetic processes in primary barley (Hordeum vulgare L.) leaves
Kaňa, R., Špundová, M., Ilı́k, P., Lazár, D., Klem, K., Tomek, P., Nauš, J., & Prášil, O. (2004) · Pesticide Biochemistry and Physiology · doi:10.1016/j.pestbp.2003.12.002 · Cited by 51
Research note: Energy partitioning in photosystem II complexes subjected to photoinhibitory treatment
Kornyeyev, D., & Hendrickson, L. (2007) · Functional Plant Biology · doi:10.1071/fp06327 · Cited by 51
Impact of two different humic substances on selected coccal green algae and cyanobacteria—changes in growth and photosynthetic performance
Bährs, H., & Steinberg, C. E. W. (2011) · Environmental Science and Pollution Research · doi:10.1007/s11356-011-0564-7 · Cited by 50
Dynamic responses of chlorophyll fluorescence parameters to drought across diverse plant families
Zait, Y., Shemer, O. E., & Cochavi, A. (2024) · Physiologia Plantarum · doi:10.1111/ppl.14527 · Cited by 49
Effects of NaCl and Na2CO3 stresses on photosynthetic ability of Chlamydomonas reinhardtii
Zuo, Z., Chen, Z., Zhu, Y., Bai, Y., & Wang, Y. (2014) · Biologia · doi:10.2478/s11756-014-0437-x · Cited by 48
Effects of soil drought stress on photosynthetic gas exchange traits and chlorophyll fluorescence in Forsythia suspensa
Lang, Y., Wang, M., Xia, J., & Zhao, Q. (2017) · Journal of Forestry Research · doi:10.1007/s11676-017-0420-9 · Cited by 48
The TL29 Protein is Lumen Located, Associated with PSII and Not an Ascorbate Peroxidase
Granlund, I., Storm, P., Schubert, M., García‐Cerdán, J. G., Funk, C., & Schröder, W. P. (2009) · Plant and Cell Physiology · doi:10.1093/pcp/pcp134 · Cited by 48
Photosynthetic responses of lettuce to downy mildew infection and cytokinin treatment
Prokopová, J., Špundová, M., Sedlářová, M., Husičková, A., Novotný, R., Doležal, K., Nauš, J., & Lebeda, A. (2010) · Plant Physiology and Biochemistry · doi:10.1016/j.plaphy.2010.04.003 · Cited by 47
Chlorophyll Fluorescence Imaging for Environmental Stress Diagnosis in Crops
Park, B., Wi, S., Chung, H., & Lee, H. (2024) · Sensors · doi:10.3390/s24051442 · Cited by 46
Salt stress change chlorophyll fluorescence in mango
de Lucena, C. C., de Siqueira, D. L., Martínez, H., & Cecon, P. R. (2012) · Revista Brasileira de Fruticultura · doi:10.1590/s0100-29452012000400034 · Cited by 46
Photosynthetic characteristics of ornamental passion flowers grown under different light intensities
Pires, M. V., de Almeida, A.-A. F., Figueiredo, A. L., Gomes, F. P., & Souza, M. M. (2011) · Photosynthetica · doi:10.1007/s11099-011-0075-2 · Cited by 46
Improvement of the rice photosynthetic apparatus defence under cadmium stress modulated by salicylic acid supply to roots
Yotsova, E. K., Dobrikova, A. G., Stefanov, M. A., Kouzmanova, M., & Apostolova, E. (2018) · Theoretical and Experimental Plant Physiology · doi:10.1007/s40626-018-0102-9 · Cited by 46
Diel quenching of Southern Ocean phytoplankton fluorescence is related to iron limitation
Schallenberg, C., Strzepek, R. F., Schuback, N., Clementson, L. A., Boyd, P. W., & Trull, T. W. (2020) · Biogeosciences · doi:10.5194/bg-17-793-2020 · Cited by 46
Multidisciplinary integrated field campaign to an acidic Martian Earth analogue with astrobiological interest: Rio Tinto
Gómez, F., Walter, N., Amils, R., Rull, F., Klingelhöfer, A. K., Kvíderová, J., Sarrazin, P. C., Foing, B. H., Behar, A., Fleischer, I., et al. (2011) · International Journal of Astrobiology · doi:10.1017/s147355041100005x · Cited by 45
The dominant modes of action of macrocidins, bioherbicidal metabolites of Phoma macrostoma , differ between susceptible plant species
Hubbard, M., TAYLOR, W. G., Bailey, K. L., & Hynes, R. K. (2016) · Environmental and Experimental Botany · doi:10.1016/j.envexpbot.2016.08.009 · Cited by 45
Effect of soil mercury pollution on ginger (Zingiber officinale Roscoe): Growth, product quality, health risks and silicon mitigation
Xu, J., Zhang, J., Lv, Y., Xu, K., Lu, S., Liu, X., & Yang, Y. L. (2020) · Ecotoxicology and Environmental Safety · doi:10.1016/j.ecoenv.2020.110472 · Cited by 45
Vegetative growth, compatible solute accumulation, ion partitioning and chlorophyll fluorescence of 'Malas-e-Saveh' and 'Shishe-Kab' pomegranates in response to salinity stress
Khayyat, M., Tehranifar, A., Davarynejad, G. H., & Sayyari‐Zahan, M. H. (2014) · Photosynthetica · doi:10.1007/s11099-014-0034-9 · Cited by 45
A model of chlorophyll fluorescence in microalgae integrating photoproduction, photoinhibition and photoregulation
Nikolaou, A., Bernardi, A., Meneghesso, A., Bezzo, F., Morosinotto, T., & Chachuat, B. (2014) · Journal of Biotechnology · doi:10.1016/j.jbiotec.2014.12.001 · Cited by 45
Inhibitory Effect of Fluoranthene on Photosynthetic Processes in Lichens Detected by Chlorophyll Fluorescence
Kummerová, M., Barták, M., Dubová, J., Třı́ska, J., Zubrová, E., & Zezulka, Š. (2005) · Ecotoxicology · doi:10.1007/s10646-005-0037-1 · Cited by 45
Ozone stress in Melissa officinalis plants assessed by photosynthetic function
Pellegrini, E., Carucci, M. G., Campanella, A., Lorenzini, G., & Nali, C. (2010) · Environmental and Experimental Botany · doi:10.1016/j.envexpbot.2010.10.006 · Cited by 45
Manganese as a site factor for epiphytic lichens
Hauck, M., & Paul, A. (2005) · The Lichenologist · doi:10.1017/s0024282905014933 · Cited by 45
Photosynthetic responses of durum wheat to chemical/microbiological fertilization management under salt and drought stresses
Khanghahi, M. Y., Leoni, B., & Crecchio, C. (2021) · Acta Physiologiae Plantarum · doi:10.1007/s11738-021-03289-z · Cited by 44
Salt-tolerant endophytic bacterium Enterobacter ludwigii B30 enhance bermudagrass growth under salt stress by modulating plant physiology and changing rhizosphere and root bacterial community
Wei, H., He, W., Li, Z., Ge, L., Zhang, J., & Liu, T. (2022) · Frontiers in Plant Science · doi:10.3389/fpls.2022.959427 · Cited by 44
Nitric oxide synthase-dependent nitric oxide production enhances chilling tolerance of walnut shoots in vitro via involvement chlorophyll fluorescence and other physiological parameter levels
Dong, N., Li, Y., Qi, J., Chen, Y., & Hao, Y. (2017) · Scientia Horticulturae · doi:10.1016/j.scienta.2017.11.016 · Cited by 43
Light Intensity: The Role Player in Cucumber Response to Cold Stress
Ashrostaghi, T., Aliniaeifard, S., Shomali, A., Azizinia, S., Kohpalekani, J. A., Moosavi-Nezhad, M., & Gruda, N. S. (2022) · Agronomy · doi:10.3390/agronomy12010201 · Cited by 43
Desiccation tolerance and lichenization: a case study with the aeroterrestrial microalga Trebouxia sp. (Chlorophyta)
Carniel, F. C., Zanelli, D., Bertuzzi, S., & Tretiach, M. (2015) · Planta · doi:10.1007/s00425-015-2319-z · Cited by 43
Non-Radiative Dissipation of Absorbed Excitation Energy Within Photosynthetic Apparatus of Higher Plants
Štroch, M., Špunda, V., & Kurasová, I. (2004) · Photosynthetica · doi:10.1023/b:phot.0000046149.97220.18 · Cited by 43
Effects of a glyphosate-based herbicide on Fucus virsoides (Fucales, Ochrophyta) photosynthetic efficiency
Falace, A., Tamburello, L., Guarnieri, G., Kaleb, S., Papa, L., & Fraschetti, S. (2018) · Environmental Pollution · doi:10.1016/j.envpol.2018.08.053 · Cited by 42
Temperature-dependent toxicities of nano zinc oxide to marine diatom, amphipod and fish in relation to its aggregation size and ion dissolution
Wong, S. W. Y., & Leung, K. (2013) · Nanotoxicology · doi:10.3109/17435390.2013.848949 · Cited by 42
PSII photochemistry is the primary target of oxidative stress imposed by ozone in Tilia americana
Pellegrini, E. (2013) · Urban forestry & urban greening · doi:10.1016/j.ufug.2013.10.006 · Cited by 42
Mesophyll freezing and effects of freeze dehydration visualized by simultaneous measurement of IDTA and differential imaging chlorophyll fluorescence
Hacker, J., Spindelböck, J. P., & Neuner, G. (2008) · Plant Cell & Environment · doi:10.1111/j.1365-3040.2008.01881.x · Cited by 42
Chlorophyll fluorescence in rice: probing of senescence driven changes of PSII activity on rice varieties differing in grain yield capacity
Falqueto, A. R., Silva, F. S. P., Cassol, D., Júnior, A. M. D. M., de Oliveira, A. C., & Bacarin, M. A. (2010) · Brazilian Journal of Plant Physiology · doi:10.1590/s1677-04202010000100004 · Cited by 41
Transcriptomics and physiological analyses reveal co-ordinated alteration of metabolic pathways inJatropha curcasdrought tolerance
Sapeta, H., Lourenço, T. F., Lorenz, S., Grumaz, C., Kirstahler, P., Barros, P. M., Costa, J. M., Sohn, K., & Oliveira, M. M. (2015) · Journal of Experimental Botany · doi:10.1093/jxb/erv499 · Cited by 40
Effects of salinity stress on the growth and chlorophyll fluorescence of Phaeodactylum tricornutum and Chaetoceros gracilis (Bacillariophyceae)
Liang, Y., Sun, M., Chuanyuan, T., Chunhui, C., & Li, Z. (2014) · Botanica Marina · doi:10.1515/bot-2014-0037 · Cited by 40
Different Sensitivity Levels of the Photosynthetic Apparatus in Zea mays L. and Sorghum bicolor L. under Salt Stress
Stefanov, M. A., Rashkov, G. D., Yotsova, E. K., Borisova, P. B., Dobrikova, A. G., & Apostolova, E. (2021) · Plants · doi:10.3390/plants10071469 · Cited by 40
Photosynthetic response of different pea cultivars to low and high temperature treatments
Georgieva, K., & Lichtenthaler, H. K. (2006) · Photosynthetica · doi:10.1007/s11099-006-0073-y · Cited by 40
Injured and uninjured leaf photosynthetic responses after mechanical injury on Nerium oleander leaves, and Danaus plexippus herbivory on Asclepias curassavica leaves
Delaney, K. J. (2008) · Plant Ecology · doi:10.1007/s11258-008-9423-0 · Cited by 40
Seasonal effects on the relationship between photosynthesis and leaf carbohydrates in orange trees
Ribeiro, R. V., Machado, E. C., Habermann, G., Santos, M. G., & de Oliveira, R. F. (2012) · Functional Plant Biology · doi:10.1071/fp11277 · Cited by 40
Effects of water stress on photosynthesis and nitrogen metabolism in vegetative and reproductive shoots of Leymus chinensis
Xu, Z., & Zhou, G. S. (2005) · Photosynthetica · doi:10.1007/s11099-005-0035-9 · Cited by 40
Interactions between iron and titanium metabolism in spinach: A chlorophyll fluorescence study in hydropony
Cígler, P., Olejníčková, J., Hrubý, M., Cséfalvay, L., Peterka, J., & Kužel, S. (2010) · Journal of Plant Physiology · doi:10.1016/j.jplph.2010.06.021 · Cited by 39
Sensitivity of physiological and biochemical endpoints in early ontogenetic stages of crops under diclofenac and paracetamol treatments
Zezulka, Š., Kummerová, M., Babula, P., Hájková, M., & Oravec, M. (2018) · Environmental Science and Pollution Research · doi:10.1007/s11356-018-3930-x · Cited by 39
The role of isoflavone metabolism in plant protection depends on the rhizobacterial MAMP that triggers systemic resistance against Xanthomonas axonopodis pv. glycines in Glycine max (L.) Merr. cv. Osumi
Algar, E., Gutiérrez‐Mañero, F. J., García‐Villaraco, A., García‐Seco, D., Lucas, J. A., & Ramos‐Solano, B. (2014) · Plant Physiology and Biochemistry · doi:10.1016/j.plaphy.2014.05.001 · Cited by 39
Performance of Siberian elm (Ulmus pumila) on steppe slopes of the northern Mongolian mountain taiga: Drought stress and herbivory in mature trees
Dulamsuren, C., Hauck, M., Nyambayar, S., Bader, M. K., Osokhjargal, D., Oyungerel, S., & Leuschner, C. (2009) · Environmental and Experimental Botany · doi:10.1016/j.envexpbot.2008.12.020 · Cited by 39
Sugarcane performance under phosphorus deficiency: physiological responses and genotypic variation
Zambrosi, F. C. B., Ribeiro, R. V., Marchiori, P. E. R., Cantarella, H., & Landell, M. G. D. A. (2014) · Plant and Soil · doi:10.1007/s11104-014-2252-0 · Cited by 39
Photosynthesis in chlorolichens: the influence of the habitat light regime
Piccotto, M., & Tretiach, M. (2010) · Journal of Plant Research · doi:10.1007/s10265-010-0329-2 · Cited by 39
Effects on the Photosynthetic Activity of Algae after Exposure to Various Organic and Inorganic Pollutants: Review
Petsas, A. S., & Vagi, M. C. (2017) · InTech eBooks · doi:10.5772/67991 · Cited by 38
High Temperature Alters Secondary Metabolites and Photosynthetic Efficiency in Heracleum sosnowskyi
Rysiak, A., Dresler, S., Hanaka, A., Hawrylak-Nowak, B., Strzemski, M., Kováčik, J., Sowa, I., Latalski, M., & Wójciak, M. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22094756 · Cited by 38
Comprehensive understanding of regulatory mechanisms, physiological models and key enzymes in microalgal cells based on various concentrations of CO2
Wang, Z., Cheng, J., Sun, Y., Jia, D., Tang, Y., Yang, W., & Cen, K. (2022) · Chemical Engineering Journal · doi:10.1016/j.cej.2022.140233 · Cited by 38
Growth and photosynthetic activity of Botryococcus braunii biofilms
Wijihastuti, R. S., Moheimani, N. R., Bahri, P. A., Cosgrove, J. J., & Watanabe, M. M. (2016) · Journal of Applied Phycology · doi:10.1007/s10811-016-1032-z · Cited by 38
Response of carbon assimilation and chlorophyll fluorescence to soybean leaf phosphorus across CO2: Alternative electron sink, nutrient efficiency and critical concentration
Singh, S. K., & Reddy, V. R. (2015) · Journal of Photochemistry and Photobiology B Biology · doi:10.1016/j.jphotobiol.2015.08.021 · Cited by 37
LIMITAÇÕES FOTOSSINTÉTICAS EM FOLHAS DE PLANTAS DE TOMATEIRO SUBMETIDAS A CRESCENTES CONCENTRAÇÕES SALINAS - DOI: 10.13083/1414-3984.v22n02a05
Tatagiba, S. D., de Moraes, G. A. B. K., Nascimento, K. J. T., & Peloso, A. F. (2014) · Revista Engenharia na Agricultura - REVENG · doi:10.13083/reveng.v22i2.488 · Cited by 37
Effects of phosphorus sources on volatile organic compound emissions from Microcystis flos-aquae and their toxic effects on Chlamydomonas reinhardtii
Zuo, Z., Yang, Y., Xu, Q., Yang, W., Zhao, J., & Zhou, L. (2017) · Environmental Geochemistry and Health · doi:10.1007/s10653-017-0055-y · Cited by 37
Circadian Rhythms and Redox State in Plants: Till Stress Do Us Part
Guadagno, C. R., Ewers, B. E., & Weinig, C. (2018) · Frontiers in Plant Science · doi:10.3389/fpls.2018.00247 · Cited by 37
Oxidative stress in ryegrass growing under different air pollution levels and its likely effects on pollen allergenicity
Lucas, J. A., Gutiérrez-Albanchez, E., Alfaya, T., Feo-Brito, F., & Gutiérrez‐Mañero, F. J. (2018) · Plant Physiology and Biochemistry · doi:10.1016/j.plaphy.2018.12.018 · Cited by 37
Soil salinity increases the tolerance of excessive sulfur fumigation stress in tomato plants
Jiang, Y., Ding, X., Zhang, D., Deng, Q., Yu, C., Zhou, S., & Hui, D. (2016) · Environmental and Experimental Botany · doi:10.1016/j.envexpbot.2016.10.002 · Cited by 37
Effects of powdery mildew infection on chloroplast and mitochondrial functions in rubber tree
Wang, L., Wang, M., & Zhang, Y. (2014) · Tropical Plant Pathology · doi:10.1590/s1982-56762014000300008 · Cited by 36
Effect of chitin and chitosan hexamers on growth and photosynthetic characteristics of wheat seedlings
LI, K. C., ZHANG, X. Q., Yu, Y., Xing, R., Liu, S., & LI, P. C. (2020) · Photosynthetica · doi:10.32615/ps.2020.021 · Cited by 36
Iron Limitation Drives the Globally Extreme Fluorescence/Chlorophyll Ratios of the Southern Ocean
Schallenberg, C., Strzepek, R. F., Bestley, S., Wojtasiewicz, B., & Trull, T. W. (2022) · Geophysical Research Letters · doi:10.1029/2021gl097616 · Cited by 36
Rhizosphere effect of nanoscale zero‐valent iron on mycorrhiza‐dependent maize assimilation
Yang, Y., Zhu, Y., Naseer, M., Wang, Q., Li, G., Tao, H., Zhu, S., Wang, B., Wang, W., & Xiong, Y. (2022) · Plant Cell & Environment · doi:10.1111/pce.14478 · Cited by 36
Adaptive photosynthetic and physiological responses to drought and rewatering in triploid Populus populations
Liao, T., Wang, Y., Xu, C., Li, Y., & Kang, X. (2017) · Photosynthetica · doi:10.1007/s11099-017-0704-5 · Cited by 36
Organ specific analysis of the anaerobic primary metabolism in rice and wheat seedlings II: Light exposure reduces needs for fermentation and extends survival during anaerobiosis
Mustroph, A., Boamfa, E. I., Laarhoven, L. J. J., Harren, F. J. M., Pörs, Y., & Grimm, B. (2006) · Planta · doi:10.1007/s00425-006-0336-7 · Cited by 36
Ridge-furrow mulching combined with appropriate nitrogen rate for enhancing photosynthetic efficiency, yield and water use efficiency of summer maize in a semi-arid region of China
Li, Y., Gu, X., Li, Y., Fang, H., & Chen, P. (2023) · Agricultural Water Management · doi:10.1016/j.agwat.2023.108450 · Cited by 37
The effects of urban impervious surfaces on eco-physiological characteristics of Ginkgo biloba: A case study from Beijing, China
Song, Y., Li, F., Wang, X., Xu, C., Zhang, J., Liu, X., & Zhang, H. (2015) · Urban forestry & urban greening · doi:10.1016/j.ufug.2015.10.008 · Cited by 35
Functional Leaf Traits and Diurnal Dynamics of Photosynthetic Parameters Predict the Behavior of Grapevine Varieties Towards Ozone
Pellegrini, E., Campanella, A., Paolocci, M., Trivellini, A., Gennai, C., Muganu, M., Nali, C., & Lorenzini, G. (2015) · PLoS ONE · doi:10.1371/journal.pone.0135056 · Cited by 36
Silicon mitigates nutritional stress in quinoa (Chenopodium quinoa Willd.)
Sales, A. C., Campos, C. N. S., Júnior, J. P. D. S., da Silva, D. L., Oliveira, K. S., Prado, R. D. M., Teodoro, L. P. R., & Teodoro, P. E. (2021) · Scientific Reports · doi:10.1038/s41598-021-94287-1 · Cited by 35
Testing the shade tolerance of selected crops under Parkia biglobosa (Jacq.) Benth. in an agroforestry parkland in Burkina Faso, West Africa
Pouliot, M., Bayala, J., & Ræbild, A. (2011) · Agroforestry Systems · doi:10.1007/s10457-011-9411-6 · Cited by 35
Effects of calcium particle films and natural shading on ecophysiological parameters of conilon coffee
da Silva, P. S. O., Júnior, L. F. G. D. O., Gonzaga, M. I. S., Sena, E. D. O. A., Maciel, L. B. S., dos Santos, M. P. F., de Mattos, E. C., & Carnelossi, M. A. G. (2018) · Scientia Horticulturae · doi:10.1016/j.scienta.2018.10.010 · Cited by 35
Modeling and simulation of the initial phases of chlorophyll fluorescence from Photosystem II
Guo, Y., & Tan, J. (2010) · Biosystems · doi:10.1016/j.biosystems.2010.10.008 · Cited by 34
Anatomy and photosystem II activity of in vitro grown Aechmea blanchetiana as affected by 1-naphthaleneacetic acid
Martins, J. P. R., Rodrigues, L. C. A., Santos, E. R., Batista, B. G., Gontijo, A. B. P. L., & Falqueto, A. R. (2018) · Biologia Plantarum · doi:10.1007/s10535-018-0781-8 · Cited by 34

Authors: Roháček, K.
Affiliations: Czech Academy of Sciences (CZ)
Corresponding author: Roháček, K.
ORCID: Roháček, K.
Venue: Photosynthetica
Publisher: Institute of Experimental Botany
Published: 2002-03-01
Volume: 40
Issue: 1
Pages: 13-29
ISSN: 0300-3604 (ISSN-L)
1573-9058
DOI: 10.1023/a:1020125719386
OpenAlex: W1571556317
Cited by: 724
References: 67
Citations by year: 2026: 27 · 2025: 35 · 2024: 31 · 2023: 35 · 2022: 33 · 2021: 35 · 2020: 39 · 2019: 28 · 2018: 36 · 2017: 40 · 2016: 31 · 2015: 36 · 2014: 51 · 2013: 36 · 2012: 33
FWCI: 4.16
Type: journal article
Language: en
Open access: bronze
doi.org
Locations: Photosynthetica (publishedVersion)
Topics: Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Photosynthetic Processes and Mechanisms
Physical Sciences › Chemistry › Physical and Theoretical Chemistry › Photochemistry and Electron Transfer Studies
Physical Sciences › Environmental Science › Global and Planetary Change › Plant Water Relations and Carbon Dynamics
Keywords: photosystem II, maximum quantum yield, photochemical quenching, non-photochemical quenching, non-radiative energy dissipation, thylakoid membranes, light adaptation, seedlings, Norway spruce

About these checks

Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.

Statistics and arithmetic are recomputed, not judged.

Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.

What counts as a claim ›How we measure confidence ›How we check this ›

Are you an author, or do you see a problem with this page? Request a review

Chlorophyll Fluorescence Parameters: The Definitions, Photosynthetic Meaning, and Mutual Relationships

Abstract

Overview

Integrity signals

Verification

Claims the paper makes

Claims other papers make about this one

Citations

Cites

Cited by

Related

Metadata

Record

About these checks