Document Type : Review Article

Author

Assistance Professor in Dryland Agriculture Research Institute, AREEO, Maragheh, Iran

Abstract

Introduction
Plants in the environment are affected by various stresses, depending on the duration, intensity and growth stage of the plant, these stresses can reduce the process of photosynthesis and affect their growth and performance. However, traditional methods, even technically advanced ones such as the measurements of photosynthetic rates through the gas exchange (CO2, H2O, and O2), are time-consuming and provide incomplete information on overall photosynthetic function. The development of knowledge in the field of chlorophyll fluorescence shows that this indicator has a high ability to study the photochemical efficiency of plant photosynthesis.
Methods
For measuring the chlorophyll fluorescence in plants, leaves were dark-adapted for 30 minutes using leaf clips provided by the producer of handy-PEA. Measurements were performed on the middle of plant leaves following the standard protocol with illumination with continuous red light (peak in 650 nm wavelength; the spectral line half-width of 22 nm) provided by an array of three light-emitting diodes. The light pulse intensity used was 3500 μmol(photon).m–2s–1 and the duration of the light pulse was 1 s. The measured data were used for the calculation of the photosynthetic parameters using Biolyzer v. 3.06 HP software (a software provided with handy-PEA). Some of the parameters we discussed in this article due to their significance are FO = minimum fluorescence, FM = maximum fluorescence, FO/FM = The maximum quantum yield of basal non-photochemical energy losses, FV/FM = the maximum quantum efficiency of PSII, VJ = the relative variable fluorescence in step J after 2 ms, VI = the relative variable fluorescence in step I after 30 ms, N = the number of QA redox turnovers until FM, SM = the pool size of the electron acceptors on the reducing side of PSII, PIABS = performance index.
Main Findings
The study of chlorophyll fluorescence can analyze with high detail the function and state of PSII reaction centres, and light-harvesting complexes. This index has a high correlation with other physiological parameters under different environmental stresses. In this article, an overview of the results of chlorophyll fluorescence analysis of crops underenvironmental stressesis given, and the key steps to stresses are presented. Under drought stress the ratio of active reaction centers in chlorophyll, primary photochemical reactions, and electron transfer are affected. By salinity stress in crops, the values of variable and, maximum fluorescence, the energy required to close the reaction centers, and the photosynthetic efficiency index decrease, while the time required to reach the maximum fluorescence increases. Under cold stress conditions, electron transfer flow per reactive centers, the quantum performance of photosystem II, and the efficiency of the water splitting complex in photosystem II decrease. Potassium affects light-dependent steps such as the size of receiving antennae and the electron connection of photosystem II reaction centers. The electron acceptor part of photosystem II is the main site of inhibition of photosynthetic electron transfer under the application of herbicides.
Conclusion and Implications
This article has provided an overview of the information about the wide opportunities of using the chlorophyll fluorescence technique in plant science, agriculture and ecological research. The measured parameters of chlorophyll fluorescence are called the JIP-test and its analysis can be used to evaluate the effects of environmental stresses on plants. This technique requires more practical studies in biotic and even non-biotic stress conditions to provide reliable information to investigate the growth and development of plants, and this leads to an increase in our knowledge of the physiological basis of crop photosynthesis under stress conditions.

Keywords

Main Subjects

Allen, D.J., Ort, D.R., 2001. Impacts of chilling temperatures on photosynthesis in warm climate plants. Trends in Plant Science, 6, 36-42. https://doi.org/10.1016/s1360-1385(00)01808-2
Ashraf, M., Bhatti, A.S., 2000. Effect of salinity on growth and chlorophyll content of rice. Pakistan Journal of Science and Industrial Research, 43, 130-141.
Baker, N.R., 2008. Chlorophyll fluorescence: A probe of photosynthesis in vivo. Annual Review of Plant Biology,  59, 89–113. https://doi.org/10.1146/annurev.arplant.59.032607.092759
Baker, N.R., Rosenqvist, E., 2004. Applications of chlorophyll fluorescence can improve crop production strategies: an examination of future possibilities. Journal of Experimental Botany, 55, 1607–1621.  https://doi.org/10.1093/jxb/erh196
Bissati, K. E., Delphin E., Murata N., Etienne A. L., Kirilovsky, D., 2000. Photosystem II fluorescence quenching in cyanobacterrium Synechocystis PCC6803: involvement of two different mechanisms. Biochimica et Biophysica Acta, 1457, 229-242.  https://doi.org/10.1016/S0005-2728(00)00104-3
Chaves, M.M., Flexas, J., Pinheiro, C., 2009. Photosynthesis under drought and salt stress: regulation mechanisms from whole plant to cell. Annals of Botany, 103, 551–560.  https://doi.org/10.1093/aob/mcn125
Christensen, M.G., Teicher, H.B., Streibig, J.C., 2003. Linking fluorescence induction curve and biomass in herbicide screening. Pest Management Science, 59,1303–1310. https://doi.org/10.1002/ps.763
Dai, F., Zhou, M., Zhang, G., 2007. The changes of chlorophyll fluorescence parameters in winter barley during recovery after freezing shock and as affected by cold acclimation and irradiance. Plant Physiology and Biochemictry, 45, 915-921. https://doi.org/10.1016/j.plaphy.2007.09.006
Dayan, E., Zaccaro, M.L.M., 2012. Chlorophyll fluorescence as a marker for herbicide mechanisms of action. Pesticide Biochemistry and Physiolog, 102, 189–197. https://doi.org/10.1016/j.pestbp.2012.01.005
FAO. 2017. Agriculture and Consumer Protection Department (FAO), Rome, https://www.fao.org/ag/ca/
Farooq, M., Wahid, A., Kobayashi, N., Fujita, D., Basra, S.M.A., 2009. Plant drought stress: Effects, Mechanisims, and Management. Sustanable Agriculture, pp, 153-188. https://doi.org/10.1051/agro:2008021
Flexas, J., Badger, M., Chow, W.S., Medrano, H., Osmond, C.B., 1999. Analysis of the relative increase in photosynthetic O2 uptake when photosynthesis in grapevine leaves is inhibited following low night temperatures and/or water stress. Plant Physiology, 121, 675-684. https://doi.org/10.1104/pp.121.2.675
GhaSsemi-Masarmi, A., Solouki, M., Golkari, S., Mahdinezhad, N., Kalaji, M.H., Fakheri, B., Jabbari, M., 2022. Comparison of photosystem II yield in Iranian native wheat genotypes using chlorophyll fluorescence parameters under salinity stress. Plant Production and Genetics, 3, 67-84. [In Persian]. https://doi.org/10.34785/J020.2022.154
Ghassemi-Golezani, K., Khomari, S., Valizadeh, M., Alyari, H., 2008. Effects of seed vigour and the duration of cold acclimation on freezing tolerance of winter oilseed rape. Seed Science and Technology, 36, 767-775.  https://doi.org/10.15258/sst.2008.36.3.26
Ghassemi-Golezani, K., Lotfi, R., 2012. Responses of soybean leaves and grain yield to water stress at reproductive stages. International Journal of Plant, Animal Environmental Sciences, 2, 63-68.
Goncalves, J.F.C., Santos, U.M., 2005. Utilization of the chlorophyll a fluorescence technique as a tool for selecting tolerant species to environment of high irradiance. Brazilian Journal of Plant Physiology, 17, 307-313.  https://doi.org/10.1590/S1677-04202005000300005
Govindjee, H., 1995. Sixtythree years since Kautsky: chlorophyll a fluorescence. Austoralian Journal of Plant Physiology, 22, 131-160. https://doi.org/10.1071/PP9950131
Hassannejad, S., Lotfi, R., Ghafarbi, SP., Oukarroum, A., Abbasi, A., Kalaji, H.M., Rastogi, A., 2020. Early identification of herbicide modes of action by the use of chlorophyll fluorescence measurements. Plants. 9, 529.  https://doi.org/10.3390/plants9040529
Hawkesford, M., Horst, W., Kichey, T., Lambers, H., Schjoerring, J., Skrumsager- Moller, I., White, P., 2012. Function of macronutrients. In: Marschner, P. (Ed.), Marschner’s Mineral Nutrition of Higher Plants. Academic Press, London, pp, 135–189.  https://doi.org/10.1016/B978-0-12-384905-2.00006-6
He, J.X., Wang J., Liang H.G., 1995. Effects of water stress on photochemical function and protein metabolism of photosystem II in wheat leaves. Physiologia Plantarum, 93, 771-777.  https://doi.org/10.1111/j.1399-3054.1995.tb05130.x
He, H., Khan, S., Deng, Y., Hu, H., Yin, L., Huang, J., 2022. Supplemental Foliar Applied Magnesium Reverted Photosynthetic Inhibition and Improved Biomass Partitioning in Magnesium Deficient Banana. Horticulturae, 8, 1050.  https://doi.org/10.3390/horticulturae8111050
Hermans, C., Smeyers, M., Rodriguez, R.M., Eyletters, M., Strasser, R.J., Delhaye, J.P., 2003. Quality assessment of urban trees: A comparative study of physiological characterization, airborne imaging and on site fluorescence monitoring by the OJIP-test. Journal of Plant Physiology, 160, 81-90. https://doi.org/10.1078/0176-1617-00917
Hermans, C., Verbruggen, N., 2005. Physiological characterization of Mg deficiency in Arabidopsis thaliana. Journal of Experimental Botany, 56, 2153–2161.  https://doi.org/10.1093/jxb/eri215
Hernandez, J.A., Jimenez, A., Mullineaux, P. Sevilla, F., 2000. Tolerance of pea to long-term salt stress is associated with induction of antioxidant defense. Plant Cell and Environment, 23, 853-862.  https://doi.org/10.1046/j.1365-3040.2000.00602.x
Homann, P., 1967. Studies on the Manganese of the Chloroplast. Plant Physiology, 42, 997–1007. https://doi.org/10.1104/pp.42.7.997
Iyengar, E.R.R., Reddy, M.P., 1996. Photosynthesis in Highly Salt-Tolerant Plants. In: Pessaraki, M., Ed., Handbook of Photosynthesis, Marcel Dekker, New York, 897-909.
Jedmowski, C., Ashoub, A., Bru¨ggemann, W., 2013. Reactions of Egyptian landraces of Hordeum vulgare and Sorghum bicolor to drought stress, evaluated by the OJIP fluorescence transient analysis. Acta Physiologiae Plantarum 35, 345–354. https://doi.org/10.1007/s11738-012-1077-9
Jin, S.H., Huang, J.Q., Li, X.Q., Zheng, B.S., Wu, J.S., Wang, Z.J., Liu, G.H., Chen, M., 2011. Effects of potassium supply on limitations of photosynthesis by mesophyll diffusion conductance in Carya cathayensis. Tree Physiology, 31, 1142–1151. https://doi.org/10.1093/treephys/tpr095
Jin, X., Yang, G., Tan, C., Zhao, C., 2015. Effects of nitrogen stress on the photosynthetic CO2 assimilation, chlorophyll fluorescence, and sugar-nitrogen ratio in corn. Scientific Report, 2, 9311. https://doi.org/10.1038/srep09311
Kafi, M., Borzoei, A., Salehi, M., Kamandi, A., Masumi, A., Nabati, J., 2009. Physiology of environmental stress in plants. Publications University of Mashhad, Iran. [In Persian].
Kalaj, H.H., Govindjee. Bosa, K., Koscielniak, J., Zuk-Golaszewska, K., 2010. Effects of salt stress on photosystem II efficiency and CO2 assimilation of two Syrian barley landraces. Environmental and Experimental Botany, 64, 214-225. https://doi.org/10.1016/j.envexpbot.2010.10.009
Kalaji, H.M., Jajoo A., Oukarroum A., Brestic M., Zivcak M., Samborska I.A., Cetner, M.D., Łukasik, Goltsev I.V., Ladle R.J., 2016. Chlorophyll a fluorescence as a tool to monitor physiological status of plants under abiotic stress conditions. Acta Physiologia Plantarum, 38,102. https://doi.org/10.1007/s11738-016-2113-y
Kalaji, H.M., Rastogi, A., Živčák, M., Brestic, M., Daszkowska Golec, A., Sitko, K., Alsharafa, K.Y., Lotfi, R., Stypiński, P., Samborska, I.A., Cetner, M.D., 2018. Prompt chlorophyll fluorescence as a tool for crop phenotyping: an example of barley landraces exposed to various abiotic stress factors. Photosynthetica, 56, 953–961. https://doi.org/10.1007/s11099-018-0766-z
Kao, W., Tsai, T.T., Tsai, H.C., Shih, C.N., 2006. Response of three Glycine sepecies to salt stress. Environmental and Experimental Botany, 20, 120-125. https://doi.org/10.1016/j.envexpbot.2005.01.009
Kazan, H., Hobikoğlu, E.H., Karademir, H., Dalyancı, L., Turguter, Y., 2015. Economic Development of Ski Industry in Experimental Innovation: Example of Palandöken Turkey and ALP Switzerland. Procedia-Social and Behavioral Sciences, 195, 487-492. https://doi.org/10.1016/j.sbspro.2015.06.245
Khoshro, HH., Lotfi, R., 2021. Advanced Breeding Approaches for Cold-Tolerant Chickpea and Lentil in Dryland Areas. IntechOpen Book.  https://doi.org/10.5772/intechopen.100516
Kocheva, K., Lambrev, P., Georgiev, G., Goltsev, V., Karabaliev, M., 2004. Evaluation of chlorophyll fluorescence and membrane injury in the leaves of barley cultivars under osmotic stress. Bioelectrochemistry, 63, 121-124. https://doi.org/10.1016/j.bioelechem.2003.09.020
Laing, W., Greer, D., Sun, O., Beets, P., Lowe, A., Payn, T., 2000. Physiological impacts of Mg deficiency in Pinusradiata: growth and photosynthesis. New Phytologist, 146, 47-57.  https://doi.org/10.1046/j.1469-8137.2000.00616.x
Lotfi, R., Abbasi, A., Valizadeh, G., Sadeghzadeh, B., Golkari, S., Eslami, R., Valizadeh, M., 2021. Evaluation of the physiological response of dryland wheat varieties to cold stress under conservation and conventional agricultural conditions. Final Report in DARI, N: 59660, pp: 1-28.
Lotfi, R., Abbasi, A., Kalaji, HM., Eskandari, I., Sedghieh, V., Khorsandi, H., Sadeghian, N., Yadav, S., Rastogi, A., 2022. The role of potassium on drought resistance of winter wheat cultivars under cold dryland conditions: Probed by chlorophyll a fluorescence. Plant Physiology and Biochemistry, 182, 45-54.  https://doi.org/10.1016/j.plaphy.2022.04.010
Lotfi, R., Ghassemi-Golezani, K., Pessarakli, M., 2020. Salicylic acid regulates photosynthetic electron transfer and stomatal conductance of mung bean (Vigna radiata L.) under salinity stress. Biocatalysis and Agricultural Biotechnology, 26, 101635.  https://doi.org/10.1016/j.bcab.2020.101635
Lotfi, R., Kalaji, H.M., Valizaeh, G.R., Khalilvand, E., Hemmati, A., Gharavi, P., Ghassemi, A., Rastogi, A., 2018. Effects of humic acid on photosynthetic efficiency of rapeseed plants growing under different watering conditions. Photosynthetica, 56, 962-970. https://doi.org/10.1007/s11099-017-0745-9
Lotfi, R., Pessarakli, M., Gharavi-Kouchebagh, P., Khoshvaghti, H., 2015a. Physiological responses of Brassica napus to fulvic acid under water stress: Chlorophyll a fluorescence and antioxidant enzyme activity. The Crop Journal, 3, 434-439.  https://doi.org/10.1016/j.cj.2015.05.006
Lotfi, R., Kouchebagh, G., Khoshvaghti, H., 2015b. Biochemical and physiological responses of Brassica napus plants to humic acid under water stress, Russian Journal of Plant Physiology, 62, 480–486. https://doi.org/10.1134/S1021443715040123
Marschner, H., 1995. Mineral nutrition of higher plants 2nd edition. Academic, Great Britain. eBook ISBN: 9780080571874.
Mathur, S., Mehta, P., Jajoo, A., Bharti, S., 2011. Analysis of elevated temperature induced inhibition of Photosystem II using Chl A fluorescence induction kinetics. Plant Biology, 13,1–6. https://doi.org/10.1111/j.1438-8677.2009.00319.x
Maxwell, K., Johnson, G.N., 2000. Chlorophyll fluorescence a practical guide. Journal of Experimental Botany, 51, 659–668.  https://doi.org/10.1093/jexbot/51.345.659
Mehta, P., Allakhverdiev, S.I., Jajoo, A., 2010. Characterization of photosystem II heterogeneity in response to high salt stress in wheat leaves (Triticum aestivum). Photosynthesis Research, 105, 249–255. https://doi.org/10.1007/s11120-010-9588-y
Mishra, A.N., Srivastava, A., Strasser, R.J., 2001. Utilization of fast chlorophyll a technique in assessing the salt/ion sensitivity of mung bean and brassica seedlings. Journal of Plant Physiology, 158, 1173-1181.  https://doi.org/10.1078/S0176-1617(04)70144-3
Nafees, A., Shabina, S., Asim, M., Rahat, N., Noushina., 2010. Application of salicylic acid increases contents of nutrients and antioxidative metabolism in mung bean and alleviates adverse effects of salinity stress. International Journal of Plant Biology, 1, 1-12. https://doi.org/10.4081/pb.2010.e1
Netondo, G.W., Onyango, J.C., Beck, E., 2004. Sorghum and salinity: II. Gas exchange and chlorophyll fluorescence of sorghum under salt stress. Crop Science, 44, 806-811. https://doi.org/10.2135/cropsci2004.7970
Nielsen, L.W., Dahllöf, I., 2007. Direct and indirect effects of the herbicides Glyphosate, Bentazone and MCPA on eelgrass (Zostera marina). Aquatic Toxicology, 82, 47–54.  https://doi.org/10.1016/j.aquatox.2007.01.004
Oukarroum, A., Schansker, G., Strasser, R.J., 2009. Drought stress effects on Photosystem I content and Photosystem II thermotolerance analyzed using Chl A fluorescence kinetics in barley varieties differing in their drought tolerance. Physiologia Plantarum, 137,188–199. https://doi.org/10.1111/j.1399-3054.2009.01273.x
Partelli, F.L., Vieira, H.D., Viana, A.P., Batista-Santos, P., Rodrigues, A.P., Leitão, A.E., Ramalho, J.C., 2009. Low temperature impact on photosynthetic parameters of coffee genotypes. Pesquisa Agropecuária Brasileira, 44, 1404-1415. https:/doi.org/10.1590/S0100-204X2009001100006 
Pei, W., Hui, L., Roland, G., 2016. Chlorophyll fluorescence response to herbicide stress in Alopecurus myosuroides. Deutsche Arbeitsbesprechung über Fragen der Unkrautbiologie und bekämpfung, 23-25. February in Braunschweig 452, 57-67. https://doi.org/10.5073/jka.2016.452.008
Pinior, A., Grunewaldt-Stöcker, G., Alten, H., Strasser, R.J., 2005. Mycorrhizal impact on drought stress tolerance of rose plants probed by chlorophyll a fluorescence, proline content and visual scoring. Mycorrhiza, 15, 596-605.  https://doi.org/10.1007/s00572-005-0001-1
Ramalho, J.C., Quartin, V.L., Leitão, E., Campos, P.S., Carelli, M.L.C., Fahl, J.I., Nunes, M.A., 2003. Cold acclimation ability and photosynthesis among species of the tropical Coffea genus. Plant Biology, 5, 631-641.  https://doi.org/10.1055/s-2003-44688
Ramzi, B., Morales, F., Abadia, A., Gomez, J., Abadia, J., 1994. Chlorophyll fluorescence as a possible tool for salinity tolerance screening in barley (Hordeum vulgare L.). Plant Physiology, 104, 667-673. https://doi.org/10.1104/pp.104.2.667
Reezi, S., Babalar, M., Kalantari, S., 2009. Silicon alleviates salt stress, decreases malondialdehyde content and affects petal color of salt-stressed cut rose. African Journal of Biotechnology, 8, 1502-1508. https://doi.org/10.5897/AJB09.180
Sai-Kachout, S., Ben-Mansour, A., Jaffel, K., Leclere, J.C., Rejeb, M.N., Ouerghi, Z., 2009. The effect of salinity on the growth of the halophyte Atriplex Hortensis. Applied Ecology and Environmental Research, 7, 319-332. https://doi.org/10.15666/aeer/0704_319332
Salomon, E., Keren, N., 2011. Manganese limitation induces changes in the activity and in the organization of photosynthetic complexes in the cyanobacterium Synechocystis sp. strain PCC 6803. Plant Physiology, 155, 571–9.  https://doi.org/10.1104/pp.110.164269
Sayed, O.H., 2003. Chlorophyll fluorescence as a tool in cereal crop research. Photosynthetica 41, 321-330. https://doi.org/10.1023/B:PHOT.0000015454.36367.e2
Schansker, G., Srivastava, A., Govindjee, Strasse, R.J., 2003. Characterization of the 820 nm transmission signal paralleling the chlorophyll a fluorescence rise (OJIP) in pea leaves. Functional Plant Biology, 30,785–796. https://doi.org/10.1071/FP03032
Shu, S., Yuan, L. Y., Guo, S. R., Sun, J., Liu, C. J., 2012. Effects of exogenous spermidine on photosynthesis, xanthophyll cycle and endogenous polyamines in cucumber seedlings exposed to salinity. African Journal of Biotechnology, 11, 6064–6074. https://doi.org/10.5897/AJB11.1354
Silva, E.A., Damatta, F.M., Ducatti, C., Regazzi, A.J., Barros, R.S., 2004. Seasonal changes in vegetative growth and photosynthesis of Arabica coffee trees. Field Crops Research, 12, 25-34. https://doi.org/10.1016/j.fcr.2004.02.010
Singh-Tomar, R., Mathur, S., Allakhverdiev, S.I., Jajoo A., 2012. Changes in PS II heterogeneity in response to osmotic and ionic stress in wheat leaves (Triticum aestivum). Journal of Bioenergetics and Biomembranes, 44, 411-419. https://doi.org/10.1007/s10863-012-9444-1
Sowinski, P., Rudzinska-Langwald, A., Adamczyk, J., Kubica, I., Fronk, J., 2005. Recovery of maize seedling growth, development and photosynthetic efficiency after initial growth at low temperature. Journal of Plant Physiology, 162, 67-80. https://doi.org/10.1016/j.jplph.2004.03.006
Stirbet, A., Govindjee., 2012. Chlorophyll a fluorescence induction: a personal perspective of the thermal phase, the J–I–P rise. Photosynthesis Research, 113,15–61. https://doi.org/10.1007/s11120-012-9754-5
Strand, A., Foyer, C.H., Gustafsson, P., Hurry, V., 2003. Increased expression of sucrose phosphate synthase in transgenic Arabidopsis thaliana results in improved photosynthetic performance and increased freezing tolerance al low temperatures. Plant, Call and Environment, 26, 523-535.  https://doi.org/10.1046/j.1365-3040.2003.00983.x
Strasser, R.J., Srivastava, A., Govindjee, 1995. Polyphasic chlorophyll a fluorescence transient in plants and cyanobacteria. Photochemistry and Photobiology, 61, 32–42. https://doi.org/10.1111/j.1751-1097.1995.tb09240.x
Strasser, R.J., Tsimilli-Michael, M., Srivastava, A., 2004. Analysis of the chlorophyll a fluorescence transient. In: Papageorgiou G, Govindjee (eds) Advances in photosynthesis and respiration. chlorophyll a fluorescence: a signature of photosynthesis. Springer, Dordrecht, pp 321–362. https://doi.org/10.1007/978-1-4020-3218-9_12
Taiz, L., Zeiger, E., 2010. Plant Physiology. 5th Edition, Sinauer Associates Inc., Sunderland, 782 p.
Tränkner, M., Tavakol, E., Jákli, B., 2018. Functioning of potassium and magnesium in photosynthesis, photosynthate translocation and photoprotection. Physiologia Plantarum, 163, 414–431. https://doi.org/10.1111/ppl.12747
Tsimilli, M., Eggenberg, P., Biro, B., Köves, K., Vörös, I., Strasser R.J., 2000. Synergistuc and antagonistic effects of arbuscular mycorrhizal fungi and Azospirillum and Rhizobium nitrogen-fixers on the photosynthetic activity alfalfa, probed by the polyphasic chlorophyll a fluorescence transient OJIP. Applied Soil Ecology, 15, 169-182.  https://doi.org/10.1016/S0929-1393(00)00093-7
Ventrella, A., Catucc, L., Agostiano, A., 2010. Herbicides affect fluorescence and electron transfer activity of spinach chloroplasts, thylakoid membranes and isolated Photosystem II. Bioelectrochemistry, 79, 43–49. https://doi.org/10.1016/j.bioelechem.2009.10.008
Verbruggen, N., Hermans, C., 2013. Physiological and molecular responses to magnesium nutritional imbalance in plants. Plant and Soil, 368, 87–99. https://doi.org/10.1007/s11104-013-1589-0
Vermaas, W.F., Steinback, K.E., Arntzen, C.J., 1984. Characterization of chloroplast thylakoid polypeptides in the 32-kDa region: polypeptide extraction and protein phosphorylation affect binding of Photosystem II-directed herbicides. Archives of Biochemistry and Biophysics, 231, 226–232. https://doi.org/10.1016/0003-9861(84)90382-5
Yamane, Y., Kashino, Y., Koike, H., Satoh, K., 1997. Increases in the fluorescence Fo level and reversible inhibition of Photosystem II reaction center by high temperature treatments in higher plants. Photosynthesis Research, 52, 57–64. https://doi.org/10.1023/A:1005884717655
Zivcak, M., Olsovska, K., Slamka, P., Galambosova, J., Rataj, V., Shao, H.B., Brestic, M., 2014. Application of chlorophyll fluorescence performance indices to assess the wheat photosynthetic functions influenced by nitrogen deficiency. Plant Soil and Environment, 60, 210–215.   https://doi.org/10.17221/73/2014-PSE