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

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

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Roháček, K.·2002·Photosynthetica

DOI 10.1023/a:1020125719386

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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.).

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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.-

Photosynthesis under stressful environments: An overview
Ashraf, M., & Harris, P. J. C. (2013) · Photosynthetica · doi:10.1007/s11099-013-0021-6 · Cited by 2,028
Linking chlorophyll a fluorescence to photosynthesis for remote sensing applications: mechanisms and challenges
Porcar‐Castell, A., Tyystjärvi, E., Atherton, J., van der Tol, C., Flexas, J., Pfündel, E. E., Moreno, J., Frankenberg, C., & Berry, J. A. (2014) · Journal of Experimental Botany · doi:10.1093/jxb/eru191 · Cited by 1,251
Frequently asked questions about chlorophyll fluorescence, the sequel
Kalaji, H. M., Schansker, G., Brestič, M., Bussotti, F., Calatayud, Á., Ferroni, L., Goltsev, V. N., Guidi, L., Jajoo, A., Li, P., et al. (2016) · Photosynthesis Research · doi:10.1007/s11120-016-0318-y · Cited by 688
Relationship between the Heat Tolerance of Photosynthesis and the Thermal Stability of Rubisco Activase in Plants from Contrasting Thermal Environments
Salvucci, M. E., & Crafts-Brandner, S. J. (2004) · Plant Physiology · doi:10.1104/pp.103.038323 · Cited by 563
How to correctly determine the different chlorophyll fluorescence parameters and the chlorophyll fluorescence decrease ratio RFd of leaves with the PAM fluorometer
Lichtenthaler, H. K., Buschmann, C., & Knapp, M. (2005) · Photosynthetica · doi:10.1007/s11099-005-0062-6 · Cited by 540
The polyphasic chlorophyll a fluorescence rise measured under high intensity of exciting light
Lazár, D. (2006) · Functional Plant Biology · doi:10.1071/fp05095 · Cited by 343
Cadmium‐induced inhibition of photosynthesis and long‐term acclimation to cadmium stress in the hyperaccumulator Thlaspi caerulescens
Küpper, H., Aravind, P., Leitenmaier, B., Trtílek, M., & Šetlík, I. (2007) · New Phytologist · doi:10.1111/j.1469-8137.2007.02139.x · Cited by 326
Chlorophyll Fluorescence as a Tool in Cereal Crop Research
Sayed, O. H. (2003) · Photosynthetica · doi:10.1023/b:phot.0000015454.36367.e2 · Cited by 308
Algal photosynthetic responses to toxic metals and herbicides assessed by chlorophyll a fluorescence
Kumar, K. S., Dahms‬, H.-U., Lee, J., Kim, H., Lee, W. C., & Shin, K. (2014) · Ecotoxicology and Environmental Safety · doi:10.1016/j.ecoenv.2014.01.042 · Cited by 289
Blue and Red LED Illumination Improves Growth and Bioactive Compounds Contents in Acyanic and Cyanic Ocimum basilicum L. Microgreens
Lobiuc, A., Vasilache, V., Oroian, M. A., Stoleru, T., Burducea, M., Pintilie, O., & Zamfirache, M.-M. (2017) · Molecules · doi:10.3390/molecules22122111 · Cited by 273
Photosynthetic changes and protective mechanisms against oxidative damage subjected to isolated and combined drought and heat stresses in Jatropha curcas plants.
Silva, E. N., Ferreira-Silva, S. L., Fontenele, A. D. V., Ribeiro, R. V., Viégas, R. A., & Silveira, J. A. G. (2010) · Journal of Plant Physiology · doi:10.1016/j.jplph.2010.03.005 · Cited by 238
Parameters of photosynthetic energy partitioning
Lazár, D. (2014) · Journal of Plant Physiology · doi:10.1016/j.jplph.2014.10.021 · Cited by 215
Cowpea (Vigna unguiculata L. Walp.) Metabolomics: Osmoprotection as a Physiological Strategy for Drought Stress Resistance and Improved Yield
Goufo, P., Moutinho‐Pereira, J., Jorge, T. F., Correia, C. M., Oliveira, M. R., Rosa, E. A. S., António, C., & Trindade, H. (2017) · Frontiers in Plant Science · doi:10.3389/fpls.2017.00586 · Cited by 205
Long‐term Low Radiation Decreases Leaf Photosynthesis, Photochemical Efficiency and Grain Yield in Winter Wheat
Mu, H., Jiang, D., Wollenweber, B., Dai, T., Jing, Q., & Cao, W. (2009) · Journal of Agronomy and Crop Science · doi:10.1111/j.1439-037x.2009.00394.x · Cited by 198
Effects of silicon nutrition on cadmium uptake, growth and photosynthesis of rice plants exposed to low-level cadmium
Nwugo, C. C., & Huerta, A. J. (2008) · Plant and Soil · doi:10.1007/s11104-008-9659-4 · Cited by 196
Silicon-mediated alleviation of Cr(VI) toxicity in wheat seedlings as evidenced by chlorophyll florescence, laser induced breakdown spectroscopy and anatomical changes
Tripathi, D. K., Singh, V. P., Prasad, S. M., Chauhan, D. K., Dubey, N. K., & Rai, A. K. (2014) · Ecotoxicology and Environmental Safety · doi:10.1016/j.ecoenv.2014.09.029 · Cited by 195
Visualization of dynamics of plant–pathogen interaction by novel combination of chlorophyll fluorescence imaging and statistical analysis: differential effects of virulent and avirulent strains of P. syringae and of oxylipins on A. thaliana
Berger, S., Benediktyová, Z., Matouš, K., Bonfig, K. B., Mueller, M. J., Nedbal, L., & Roitsch, T. G. (2006) · Journal of Experimental Botany · doi:10.1093/jxb/erl208 · Cited by 194
Comparative effects of salinity and water stress on photosynthesis, water relations and growth of Jatropha curcas plants
Silva, E. N., Ribeiro, R. V., Ferreira‐Silva, S. L., Viégas, R. A., & da Silveira, J. A. G. (2010) · Journal of Arid Environments · doi:10.1016/j.jaridenv.2010.05.036 · Cited by 194
Chitosan antitranspirant activity is due to abscisic acid-dependent stomatal closure
Iriti, M., Picchi, V., Rossoni, M., Gomarasca, S., Ludwig, N. G., Gargano, M., & Faoro, F. (2009) · Environmental and Experimental Botany · doi:10.1016/j.envexpbot.2009.01.004 · Cited by 192
Assessing the Effects of Water Deficit on Photosynthesis Using Parameters Derived from Measurements of Leaf Gas Exchange and of Chlorophyll a Fluorescence
Urban, L., Aarrouf, J., & Bidel, L. (2017) · Frontiers in Plant Science · doi:10.3389/fpls.2017.02068 · Cited by 177
Impairment of maize seedling photosynthesis caused by a combination of potassium deficiency and salt stress
Qu, C., Liu, C., Gong, X., Li, C., Hong, M., Wang, L., & Hong, F. (2011) · Environmental and Experimental Botany · doi:10.1016/j.envexpbot.2011.08.019 · Cited by 158
Drought-induced changes in chlorophyll fluorescence, photosynthetic pigments, and thylakoid membrane proteins of Vigna radiata
Batra, N. G., Sharma, V., & Kumari, N. (2014) · Journal of Plant Interactions · doi:10.1080/17429145.2014.905801 · Cited by 157
Silicon alleviates cadmium toxicity by enhanced photosynthetic rate and modified bundle sheath's cell chloroplasts ultrastructure in maize
Vaculík, M., Pavlovič, A., & Lux, A. (2015) · Ecotoxicology and Environmental Safety · doi:10.1016/j.ecoenv.2015.05.026 · Cited by 157
Spatial-temporal variations in rose leaves under water stress conditions studied by chlorophyll fluorescence imaging
Calatayud, Á., Roca, D., & Martínez, P. F. (2006) · Plant Physiology and Biochemistry · doi:10.1016/j.plaphy.2006.09.015 · Cited by 153
Salt stress induced damages on the photosynthesis of physic nut young plants
da Silva, E. N., Ribeiro, R. V., Ferreira‐Silva, S. L., Viégas, R. A., & da Silveira, J. A. G. (2011) · Scientia Agricola · doi:10.1590/s0103-90162011000100010 · Cited by 149
Photosynthesis performance, antioxidant enzymes, and ultrastructural analyses of rice seedlings under chromium stress
Ma, J., Lv, C., Xu, M., Chen, G., Lv, C., & Gao, Z. (2015) · Environmental Science and Pollution Research · doi:10.1007/s11356-015-5439-x · Cited by 148
The effect of induced heat waves on P inus taeda and Q uercus rubra seedlings in ambient and elevated CO 2 atmospheres
Ameye, M., Wertin, T. M., Bauweraerts, I., McGuire, M. A., Teskey, R. O., & Steppe, K. (2012) · New Phytologist · doi:10.1111/j.1469-8137.2012.04267.x · Cited by 147
Photosynthesis and water relations of well-watered orange plants as affected by winter and summer conditions
Ribeiro, R. V., Machado, E. C., Santos, M. G., & Oliveira, R. F. (2009) · Photosynthetica · doi:10.1007/s11099-009-0035-2 · Cited by 146
Ozone stress in woody plants assessed with chlorophyll a fluorescence. A critical reassessment of existing data
Bussotti, F., Desotgiu, R., Cascio, C., Pollastrini, M., Gravano, E., Gerosa, G. A., Marzuoli, R., Nali, C., Lorenzini, G., Salvatori, E., et al. (2010) · Environmental and Experimental Botany · doi:10.1016/j.envexpbot.2010.10.022 · Cited by 141
Possible ecological risk of two pharmaceuticals diclofenac and paracetamol demonstrated on a model plant Lemna minor
Kummerová, M., Zezulka, Š., Babula, P., & Třı́ska, J. (2015) · Journal of Hazardous Materials · doi:10.1016/j.jhazmat.2015.09.057 · Cited by 140
Photosynthetic, antioxidative, molecular and ultrastructural responses of young cacao plants to Cd toxicity in the soil
de Araújo, R. P., de Almeida, A.-A. F., Pereira, L. S., Mangabeira, P. A. O., Junior, J. O. D. S., Pirovani, C. P., Ahnert, D., & Baligar, V. C. (2017) · Ecotoxicology and Environmental Safety · doi:10.1016/j.ecoenv.2017.06.006 · Cited by 140
Shade tolerance, photoinhibition sensitivity and phenotypic plasticity of Ilex aquifolium in continental Mediterranean sites
Valladares, F., Arrieta, S., Aranda, I., Lorenzo, D., Sánchez‐Gómez, D., Tena, D., Suárez, F., & Pardos, J. A. (2005) · Tree Physiology · doi:10.1093/treephys/25.8.1041 · Cited by 137
Effect of anthocyanins, carotenoids, and flavonols on chlorophyll fluorescence excitation spectra in apple fruit: signature analysis, assessment, modelling, and relevance to photoprotection
Merzlyak, M. N., Melø, T. B., & Naqvi, K. R. (2008) · Journal of Experimental Botany · doi:10.1093/jxb/erm316 · Cited by 134
Overview of Fluorescence Protocols: Theory, Basic Concepts, and Practice
Huot, Y., & Babin, M. (2010) · Springer eBooks · doi:10.1007/978-90-481-9268-7_3 · Cited by 134
Effects of B excess on some physiological and anatomical parameters of ‘Navelina’ orange plants grafted on two rootstocks
Papadakis, I. E., Dimassi, K. N., Bosabalidis, A. M., Therios, I. N., Patakas, A., & Giannakoula, A. E. (2003) · Environmental and Experimental Botany · doi:10.1016/j.envexpbot.2003.11.004 · Cited by 128
Beneficial rhizobacteria from rice rhizosphere confers high protection against biotic and abiotic stress inducing systemic resistance in rice seedlings
Lucas, J. A., García-Cristobal, J., Bonilla, A., Ramos‐Solano, B., & Gutiérrez‐Mañero, F. J. (2014) · Plant Physiology and Biochemistry · doi:10.1016/j.plaphy.2014.05.007 · Cited by 123
Effects of Water Stress on Fluorescence Parameters and Photosynthetic Characteristics of Drip Irrigation in Rice
Xu, Q., Ma, X., Lv, T., Meng, B., Wang, Z., & Niu, J. (2020) · Water · doi:10.3390/w12010289 · Cited by 122
A high proportion of blue light increases the photosynthesis capacity and leaf formation rate of Rosa × hybrida but does not affect time to flower opening
Terfa, M. T., Solhaug, K. A., Gislerød, H. R., Olsen, J. E., & Torre, S. (2012) · Physiologia Plantarum · doi:10.1111/j.1399-3054.2012.01698.x · Cited by 121
Non-photochemical quenching of chlorophyll fluorescence and operation of the xanthophyll cycle in estuarine microphytobenthos
Serôdio, J., Cruz, S., Vieira, S., & Brotas, V. (2005) · Journal of Experimental Marine Biology and Ecology · doi:10.1016/j.jembe.2005.05.011 · Cited by 121
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Rodea‐Palomares, I., Gonzalo, S., Santiago‐Morales, J., Leganés, F., García‐Calvo, E., Rosal, R., & Fernández‐Piñas, F. (2012) · Aquatic Toxicology · doi:10.1016/j.aquatox.2012.06.005 · Cited by 115
Photosynthetic activity, photoprotection and photoinhibition in intertidal microphytobenthos as studied in situ using variable chlorophyll fluorescence
Serôdio, J., Vieira, S., & Cruz, S. (2008) · Continental Shelf Research · doi:10.1016/j.csr.2008.03.019 · Cited by 114
Influence of foliar application of silicon on chlorophyll fluorescence, photosynthetic pigments, and growth in water-stressed wheat cultivars differing in drought tolerance
Maghsoudi, K., Emam, Y., & Ashraf, M. (2015) · TURKISH JOURNAL OF BOTANY · doi:10.3906/bot-1407-11 · Cited by 112
Bioreceptivity evaluation of cementitious materials designed to stimulate biological growth
Manso, S., Muynck, W. D., Segura, I., Aguado, A., Steppe, K., Boon, N., & Belie, N. D. (2014) · The Science of The Total Environment · doi:10.1016/j.scitotenv.2014.02.059 · Cited by 112
Effect of Dark Septate Endophytic Fungus Gaeumannomyces cylindrosporus on Plant Growth, Photosynthesis and Pb Tolerance of Maize ( Zea mays L.)
Ban, Y., Xu, Z., Yang, Y., Zhang, H., Chen, H., & Tang, M. (2017) · Pedosphere · doi:10.1016/s1002-0160(17)60316-3 · Cited by 110
Improvement of photosynthesis in rice (Oryza sativa L.) as a result of an increase in stomatal aperture and density by exogenous hydrogen sulfide treatment
Duan, B., Ma, Y., Jiang, M., Yang, F., Ni, L., & Lu, W. (2014) · Plant Growth Regulation · doi:10.1007/s10725-014-9929-5 · Cited by 107
Simulation of Pulse-Amplitude-Modulated (PAM) fluorescence: Limitations of some PAM-parameters in studying environmental stress effects
Juneau, P., Green, B. R., & Harrison, P. J. H. (2005) · Photosynthetica · doi:10.1007/s11099-005-5083-7 · Cited by 106
Changes of photosynthetic activities of maize (Zea mays L.) seedlings in response to cadmium stress
Wang, H., Zhao, S., Liu, R. L., Zhou, W., & Jin, J. (2009) · Photosynthetica · doi:10.1007/s11099-009-0043-2 · Cited by 103
On the mechanism underlying photosynthetic limitation upon trigger hair irritation in the carnivorous plant Venus flytrap (Dionaea muscipula Ellis)
Pavlovič, A., Slováková, Ľ., Pandolfi, C., & Mancuso, S. (2011) · Journal of Experimental Botany · doi:10.1093/jxb/erq404 · Cited by 100
Chlorophyll fluorescence performance of sweet almond [Prunus dulcis (Miller) D. Webb] in response to salinity stress induced by NaCl
Ranjbar, A., Samson, R., & Damme, P. V. (2006) · Photosynthetica · doi:10.1007/s11099-006-0064-z · Cited by 97
Water relations and photosynthetic performance in Larix sibirica growing in the forest-steppe ecotone of northern Mongolia
Dulamsuren, C., Hauck, M., Bader, M. K., Osokhjargal, D., Oyungerel, S., Nyambayar, S., Runge, M., & Leuschner, C. (2008) · Tree Physiology · doi:10.1093/treephys/tpn008 · Cited by 97
Homologous NF-YC2 Subunit from Arabidopsis and Tobacco Is Activated by Photooxidative Stress and Induces Flowering
Hackenberg, D., Keetman, U., & Grimm, B. (2012) · International Journal of Molecular Sciences · doi:10.3390/ijms13033458 · Cited by 96
Changes in antioxidant enzyme activities and isozyme profiles in leaves of male and female Populus cathayana infected with Melampsora larici-populina
Zhang, S., Lu, S., Xu, X., Korpelainen, H., & Li, C. (2009) · Tree Physiology · doi:10.1093/treephys/tpp094 · Cited by 96
The impact of salicylic acid and silicon on chlorophyll a fluorescence in mung bean under salt stress
Ghassemi‐Golezani, K., & Lotfi, R. (2015) · Russian Journal of Plant Physiology · doi:10.1134/s1021443715040081 · Cited by 95
Effects of light and nitrogen starvation on the content and composition of carotenoids of the green microalga Parietochloris incisa
Solovchenko, A. E., Khozin‐Goldberg, I., Didi‐Cohen, S., Cohen, Z., & Merzlyak, M. N. (2008) · Russian Journal of Plant Physiology · doi:10.1134/s1021443708040043 · Cited by 95
Cytokinin-induced changes in the chlorophyll content and fluorescence of in vitro apple leaves
Dobránszki, J., & Mendler‐Drienyovszki, N. (2014) · Journal of Plant Physiology · doi:10.1016/j.jplph.2014.06.015 · Cited by 93
Changes in the protein profile of Quercus ilex leaves in response to drought stress and recovery
Echevarría‐Zomeño, S., Ariza, D., Jorge, I., Lenz, C., del Campo, A. D., Jorrín-Novo, J. V., & Navarro, R. M. (2008) · Journal of Plant Physiology · doi:10.1016/j.jplph.2008.05.008 · Cited by 93
Effects of cytokinin on photosynthetic gas exchange, chlorophyll fluorescence parameters and antioxidative system in seedlings of eggplant (Solanum melongena L.) under salinity stress
Wu, X., Zhu, Z., Li, X., & Zha, D. (2012) · Acta Physiologiae Plantarum · doi:10.1007/s11738-012-1010-2 · Cited by 93
Nitrogen Metabolism and Photosynthesis in Leymus chinensis in Response to Long-term Soil Drought
Xu, Z., & Zhou, G. (2006) · Journal of Plant Growth Regulation · doi:10.1007/s00344-006-0043-4 · Cited by 92
Photosynthetic limitations in leaves of young Brazilian Green Dwarf coconut (Cocos nucifera L. ‘nana’) palm under well-watered conditions or recovering from drought stress
Gomes, F. P., Oliva, M. A., Mielke, M. S., de Almeida, A.-A. F., Leite, H. G., & de Aquino, L. Â. (2007) · Environmental and Experimental Botany · doi:10.1016/j.envexpbot.2007.08.006 · Cited by 91
Lemna minor exposed to fluoranthene: Growth, biochemical, physiological and histochemical changes
Zezulka, Š., Kummerová, M., Babula, P., & Váňová, L. (2013) · Aquatic Toxicology · doi:10.1016/j.aquatox.2013.05.011 · Cited by 91
Antioxidative responses of duckweed (Lemna minor L.) to short-term copper exposure
Razinger, J., Dermastia, M., Drinovec, L., Drobne, D., Zrimec, A., & Koce, J. D. (2007) · Environmental Science and Pollution Research · doi:10.1065/espr2006.11.364 · Cited by 90
Impact of foliar spray of zinc oxide nanoparticles on the photosynthesis of Pisum sativum L. under salt stress
Elshoky, H. A., Yotsova, E. K., Farghali, M. A., Farroh, K. Y., El-Sayed, K., ElZorkany, H. E., Rashkov, G. D., Dobrikova, A. G., Borisova, P. B., Stefanov, M. A., et al. (2021) · Plant Physiology and Biochemistry · doi:10.1016/j.plaphy.2021.08.039 · Cited by 89
The influence of ABA on water relation, photosynthesis parameters, and chlorophyll fluorescence under drought conditions in two maize hybrids with contrasting drought resistance
de Souza, T. C., Magalhães, P. C., de Castro, E. M., de Albuquerque, P. E. P., & Marabesi, M. A. (2012) · Acta Physiologiae Plantarum · doi:10.1007/s11738-012-1093-9 · Cited by 88
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Schuback, N., Schallenberg, C., Duckham, C., Maldonado, M. T., & Tortell, P. D. (2015) · PLoS ONE · doi:10.1371/journal.pone.0133235 · Cited by 89
Leaf Chlorophyll Fluorescence: Background and Fundamentals for Plant Biologists
Henriques, F. S. (2009) · The Botanical Review · doi:10.1007/s12229-009-9035-y · Cited by 87
Silicon‐induced cadmium resistance in rice (Oryza sativa)
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Use of chlorophyll fluorescence as a tool for determination of herbicide toxic effect: Review
Juneau, P., Qiu, B., & Deblois, C. P. (2007) · Toxicological & Environmental Chemistry Reviews · doi:10.1080/02772240701561569 · Cited by 82
Assessment of the Photosynthetic Apparatus Functions by Chlorophyll Fluorescence and P700 Absorbance in C3 and C4 Plants under Physiological Conditions and under Salt Stress
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Prey availability directly affects physiology, growth, nutrient allocation and scaling relationships among leaf traits in 10 carnivorous plant species
Farnsworth, E. J., & Ellison, A. M. (2007) · Journal of Ecology · doi:10.1111/j.1365-2745.2007.01313.x · Cited by 80
Diurnal variation in the coupling of photosynthetic electron transport and carbon fixation in iron-limited phytoplankton in the NE subarctic Pacific
Schuback, N., Flecken, M., Maldonado, M. T., & Tortell, P. D. (2016) · Biogeosciences · doi:10.5194/bg-13-1019-2016 · Cited by 78
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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

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

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