Photosynthetica 2025,63(4):322-331 | DOI: 10.32615/ps.2025.032

Additional far-red light improves the growth and resistance of the photosynthetic apparatus of Lactuca sativa L. to high-intensity light

V.D. KRESLAVSKI1, P.P. PASHKOVSKIY2, A.N. SHMAREV1, A.Yu. KHUDYAKOVA1, V.V. STROKINA1, A.A. IVANOV1, A.A. KOSOBRYUKHOV1, S.I. ALLAKHVERDIEV1, 2, 3
1 Institute of Basic Biological Problems, Russian Academy of Sciences, Institutskaya Street 2, 142290 Pushchino, Russia
2 K.A. Timiryazev Institute of Plant Physiology, Russian Academy of Sciences, Botanicheskaya Street 35, 127276 Moscow, Russia
3 Faculty of Engineering and Natural Sciences, Bahcesehir University, Istanbul, Turkey

The effects of additional far-red light (FRL) on the growth parameters, photosynthetic activity, and pro- or antioxidant balance of Lactuca sativa L. plants grown for 30 d were studied. The plants were grown under white light-emitting diodes with equal PAR intensities at red/far-red light ratios of 0.29, 0.89, and 1.67 and without FRL. Compared to the absence of the FRL, growth at a 0.29 ratio caused an increase in plant biomass and leaf area, but a decrease in PSII activity, net photosynthetic rate (PN) per unit area, and stomatal conductance. High irradiance for 4 h at 1,000 μmol(photon) m-2 s-1 decreased PSII activity and PN, but to the least extent in the 0.89 option. The possible pathways of the FRL's impact on the photosynthetic apparatus were analysed.

Additional key words: far-red light; growth; high irradiance; Lactuca sativa L.; photosynthesis; red light.

Received: July 16, 2025; Revised: September 19, 2025; Accepted: October 21, 2025; Prepublished online: November 4, 2025; Published: December 31, 2025  Show citation

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KRESLAVSKI, V.D., PASHKOVSKIY, P.P., SHMAREV, A.N., KHUDYAKOVA, A.Y., STROKINA, V.V., IVANOV, A.A., KOSOBRYUKHOV, A.A., & ALLAKHVERDIEV, S.I. (2025). Additional far-red light improves the growth and resistance of the photosynthetic apparatus of Lactuca sativa L. to high-intensity light. Photosynthetica63(4), 322-331. doi: 10.32615/ps.2025.032
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References

  1. Allakhverdiev S.I., ©etlíková E., Klimov V.V., ©etlík I.: In photoinhibited photosystem II particles pheophytin photoreduction remains unimpaired. - FEBS Lett. 226: 186-190, 1987. Go to original source...
  2. Aro E.-M., Virgin I., Andersson B.: Photoinhibition of photosystem II. Inactivation, protein damage and turnover. - BBA-Bioenergetics 1143: 113-134, 1993. Go to original source...
  3. Cao K., Yu J., Xu D. et al.: Exposure to lower red to far-red light ratios improve tomato tolerance to salt stress. - BMC Plant Biol. 18: 92, 2018. Go to original source...
  4. Carvalho R.F., Campos M.L., Azevedo R.A.: The role of phytochrome in stress tolerance. - J. Integr. Plant Biol. 53: 920-929, 2011. Go to original source...
  5. Casal J.J.: Photoreceptor signaling networks in plant responses to shade. - Annu. Rev. Plant Biol. 64: 403-427, 2013. Go to original source...
  6. Cheng M.C., Kathare P.K., Paik I., Huq E.: Phytochrome signaling networks. - Annu. Rev. Plant Biol. 72: 217-244, 2021. Go to original source...
  7. Didaran F., Kordrostami M., Ghasemi-Soloklui A.A. et al.: The mechanisms of photoinhibition and repair in plants under high light conditions and interplay with abiotic stressors. - J. Photoch. Photobio. B 259: 113004, 2024. Go to original source...
  8. Goltsev V.N., Kalaji H.M., Paunov M. et al.: Variable chlorophyll fluorescence and its use for assessing physiological condition of plant photosynthetic apparatus. - Russ. J. Plant Physiol. 63: 869-893, 2016. Go to original source...
  9. Gupta A.S., Webb R.P., Holaday A.S., Allen R.D.: Overexpression of superoxide dismutase protects plants from oxidative stress (induction of ascorbate peroxidase in superoxide dismutase overexpressing plants). - Plant Physiol. 103: 1067-1073, 1993. Go to original source...
  10. He R., Zhang Y.T., Song S.W. et al.: UV-A and FR irradiation improves growth and nutritional properties of lettuce grown in an artificial light plant factory. - Food Chem. 345: 128727, 2021. Go to original source...
  11. Hitz T., Hartung J., Graeff-Hoenninger S., Munz S.: Morphological response of soybean (Glycine max (L.) Merr.) cultivars to light intensity and red to far-red ratio. - Agronomy 9: 428, 2019. Go to original source...
  12. Holmes M.G., Smith H.: The function of phytochrome in the natural environment - I. Characterization of daylight for studies in photomorphogenesis and photoperiodism. - Photochem. Photobiol. 25: 533-538, 1977. Go to original source...
  13. Holopainen J.K., Kivimäenpää M., Julkunen-Tiitto R.: New light for phytochemicals. - Trends Biotechnol. 36: 7-10, 2018. Go to original source...
  14. Hou H.J.M., Najafpour M.M., Moore G.F., Allakhverdiev S.I.: Photosynthesis: Structures, Mechanisms, and Applications. Pp. 417. Springer, Cham 2017. Go to original source...
  15. Hu W., Franklin K.A., Sharrock R.A. et al.: Unanticipated regulatory roles for Arabidopsis phytochromes revealed by null mutant analysis. - PNAS 110: 1542-1547, 2013. Go to original source...
  16. Kochetova G.V., Avercheva O.V., Bassarskaya E.M., Zhigalova T.V.: Light quality as a driver of photosynthetic apparatus development. - Biophys. Rev. 14: 779-803, 2022. Go to original source...
  17. Kong J., Zhao Y., Fan P. et al.: Far-red light modulates grapevine growth by increasing leaf photosynthesis efficiency and triggering organ-specific transcriptome remodelling. - BMC Plant Biol. 24: 189, 2024. Go to original source...
  18. Kramer D.M., Johnson G., Kiirats O., Edwards G.E.: New fluorescence parameters for the determination of QA redox state and excitation energy fluxes. - Photosynth. Res. 79: 209-2018, 2004. Go to original source...
  19. Kreslavski V., Pashkovskiy P., Ashikhmin A. et al.: The resistance of Solanum lycopersicum photosynthetic apparatus to high-intensity blue light is determined mainly by the cryptochrome 1 content. - Photosynthetica 63: 1-9, 2025. Go to original source...
  20. Kreslavski V.D., Carpentier R., Klimov V.V., Allakhverdiev S.I.: Transduction mechanisms of photoreceptor signals in plant cells. - J. Photoch. Photobio. C 10: 63-80, 2009. Go to original source...
  21. Kreslavski V.D., Lankin A.V., Vasilyeva G.K. et al.: Effects of polyaromatic hydrocarbons on photosystem II activity in pea leaves. - Plant Physiol. Biochem. 81: 135-142, 2014. Go to original source...
  22. Kreslavski V.D., Los D.A., Schmit F.-J. et al.: The impact of the phytochromes on photosynthetic processes. - BBA-Bioenergetics 1859: 400-408, 2018. Go to original source...
  23. Lanoue J., Leonardos E.D., Grodzinski B.: Effects of light quality and intensity on diurnal patterns and rates of photo-assimilate translocation and transpiration in tomato leaves. - Front. Plant Sci. 9: 756, 2018. Go to original source...
  24. Legendre R., van Iersel M.W.: Supplemental far-red light stimulates lettuce growth: disentangling morphological and physiological effects. - Plants-Basel 10: 166, 2021. Go to original source...
  25. Li J., Li Y., Chen Y. et al.: Quantifying the effects of far-red light on lettuce photosynthesis and growth using a 3D modelling approach. - Front. Plant Sci. 15: 1492431, 2024. Go to original source...
  26. Li L., Ljung K., Breton G. et al.: Linking photoreceptor excitation to changes in plant architecture. - Gene. Dev. 26: 785-790, 2012. Go to original source...
  27. Li Q., Kubota C.: Effects of supplemental light quality on growth and phytochemicals of baby leaf lettuce. - Environ. Exp. Bot. 67: 59-64, 2009. Go to original source...
  28. Li Y., Jiang H., Gao M. et al.: Far-red-light-induced morphology changes, phytohormone, and transcriptome reprogramming of Chinese kale (Brassica alboglabra Bailey). - Int. J. Mol. Sci. 24: 5563, 2023. Go to original source...
  29. Lichtenthaler H.K.: Chlorophylls and carotenoids: pigments of photosynthetic biomembranes. -Method. Enzymol. 148: 350-382, 1987. Go to original source...
  30. Lisina T.N., Chetina O.A., Parfenkova V.A. et al.: The ratio of red to far-red light affects growth, pigment content, and photosynthetic rates in cress plants. - Russ. J. Plant Physiol. 71: 27, 2024. Go to original source...
  31. Liu C.-C., Chi C., Jin L.-J. et al.: The bZip transcription factor HY5 mediates CRY1a-induced anthocyanin biosynthesis in tomato. - Plant Cell Environ. 41: 1762-1775, 2018. Go to original source...
  32. Maehly A.C., Chance B.: The assay of catalases and peroxidases. -In: Glick D. (ed.): Methods of Biochemical Analysis. Pp. 357-424. Interscience Publishers, New York 1954. Go to original source...
  33. Meijer D., Meisenburg M., van Loon J.J.A., Dicke M.: Effects of low and high red to far-red light ratio on tomato plant morphology and performance of four arthropod herbivores. - Sci. Hortic.-Amsterdam 292: 110645, 2022. Go to original source...
  34. Murata N., Takahashi S., Nishiyama Y., Allakhverdiev S.I.: Photoinhibition of photosystem II under environmental stress. - BBA-Bioenergetics 1767: 414-421, 2007. Go to original source...
  35. Paik I., Huq E.: Plant photoreceptors: multi-functional sensory proteins and their signaling networks. - Semin. Cell Dev. Biol. 92: 114-121, 2019. Go to original source...
  36. Paradiso R., Proietti S.: Light quality manipulation to control plant growth and photomorphogenesis in greenhouse horticulture: the state of the art and the opportunities of modern LED systems. - J. Plant Growth Regul. 41: 742-780, 2022. Go to original source...
  37. Pashkovskiy P.P., Soshinkova T.N., Korolkova D.V. et al.: The effect of light quality on the pro-/antioxidant balance, activity of photosystem II, and expression of light-dependent genes in Eutrema salsugineum callus cells. - Photosynth. Res. 136: 199-214, 2018. Go to original source...
  38. Pierik R., Ballaré C.L.: Control of plant growth and defense by photoreceptors: from mechanisms to opportunities in agriculture. - Mol. Plant 14: 61-76, 2021. Go to original source...
  39. Quail P.H.: Phytochromes. - Curr. Biol. 20: R504-R507, 2010. Go to original source...
  40. Sellaro R., Crepy M., Trupkin S.A. et al.: Cryptochrome as a sensor of the blue/green ratio of natural radiation in Arabidopsis. - Plant Physiol. 154: 401-409, 2010. Go to original source...
  41. Shibuya T., Endo R., Kitamura Y. et al.: Potential photosynthetic advantages of cucumber (Cucumis sativus L.) seedlings grown under fluorescent lamps with high red:far-red light. - HortScience 45: 553-558, 2010. Go to original source...
  42. Shmarev A., Vereshagin M., Pashkovskiy P. et al.: Influence of additional far-red light on the photosynthetic and growth parameters of lettuce plants and the resistance of the photosynthetic apparatus to high irradiance. - Photosynthetica 62: 180-186, 2024. Go to original source...
  43. Smith H., Whitelam G.: The shade avoidance syndrome: multiple responses mediated by multiple phytochromes. - Plant Cell Environ. 20: 840-844, 1997. Go to original source...
  44. Tan T., Li S., Fan Y. et al.: Far-red light: a regulator of plant morphology and photosynthetic capacity. - Crop J. 10: 300-309, 2022. Go to original source...
  45. Vitale E., Velikova V., Tsonev T. et al.: Manipulation of light quality is an effective tool to regulate photosynthetic capacity and fruit antioxidant properties of Solanum lycopersicum L. cv. 'Microtom' in a controlled environment. - Peer J. 10: e13677, 2022. Go to original source...
  46. Voitsekhovskaja O.V.: Phytochromes and other (photo)receptors of information in plants. - Russ. J. Plant Physiol. 66: 351-364, 2019. Go to original source...
  47. Yang F., Liu Q., Cheng Y. et al.: Low red/far-red ratio as a signal promotes carbon assimilation of soybean seedlings by increasing the photosynthetic capacity. - BMC Plant Biol. 20: 148, 2020. Go to original source...
  48. Zhang L.-X., Li S.-X., Zhang H., Liang Z.-S.: Nitrogen rates and water stress effects on production, lipid peroxidation and antioxidative enzyme activities in two maize (Zea mays L.) genotypes. - J. Agron. Crop Sci. 193: 387-397, 2007. Go to original source...
  49. Zhen S., Bugbee B.: Substituting far-red for traditionally defined photosynthetic photons results in equal canopy quantum yield for CO2 fixation and increased photon capture during long-term studies: implications for re-defining PAR. - Front. Plant Sci. 11: 581156, 2020. Go to original source...
  50. Zhen S., Haidekker M., van Iersel M.W.: Far-red light enhances photochemical efficiency in a wavelength-dependent manner. - Physiol. Plantarum 167: 21-33, 2019. Go to original source...
  51. Zhen S., van Iersel M.W.: Far-red light is needed for efficient photochemistry and photosynthesis. - J. Plant Physiol. 209: 115-122, 2017. Go to original source...
  52. Zhen S., van Iersel M., Bugbee B.: Why far-red photons should be included in the definition of photosynthetic photons and the measurement of horticultural fixture efficacy. - Front. Plant Sci. 12: 693445, 2021. Go to original source...
  53. Zou J., Zhang Y., Zhang Y. et al.: Morphological and physiological properties of indoor cultivated lettuce in response to additional far-red light. - Sci. Hortic.-Amsterdam 257: 108725, 2019. Go to original source...