- PII
- S3034624X25030021-1
- DOI
- 10.7868/S3034624X25030021
- Publication type
- Article
- Status
- Published
- Authors
- Volume/ Edition
- Volume 72 / Issue number 3
- Pages
- 181-192
- Abstract
- using 6 species of aboriginal () and introduced () plants of the Subarctic, it was shown that under continuous lighting (CL) in climate chambers (at constant temperature, humidity, light intensity and spectral composition), plants exhibit a complex of physiological and biochemical changes similar to those that occur during natural leaf aging in nature, namely, the loss of chlorophyll and carotenoids with an increase in the chlorophyll ratio and a decrease in the chlorophyll/carotenoid ratio, a decrease in values, an increase in the content of anthocyanins, hydrogen peroxide and lipid peroxidation products. Based on the data presented in this work and previously obtained data, as well as an analysis of the literature, it was concluded that CL is not a factor inducing the senescence, as some authors suggest, but, like other stressors, causes numerous changes and disturbances in sensitive species, some of which are similar to those observed during natural aging of leaves.
- Keywords
- круглосуточное освещение растения старение фотопериодический стресс
- Date of publication
- 19.03.2026
- Year of publication
- 2026
- Number of purchasers
- 0
- Views
- 43
References
- 1. Hao X., Guo X., Lanoue J., Zhang Y., Cao R., Zheng J., Little C., Leonardos D., Kholsa S., Grodzinski B., Yelton M. A review on smart application of supplemental lighting in greenhouse fruiting vegetable production // Acta Hortic. 2018. V. 1227. P. 499–506. https://doi.org/10.17660/ActaHortic.2018.1227.63
- 2. Shibaeva T.G., Mamaev A.V., Sherudilo E.G., Titov A.F. The role of photosynthetic daily light integral in plant response to extended photoperiods // Russ. J. Plant Physiol. 2022. V. 69:7. https://doi.org/10.1134/S1021443722010216
- 3. Sysoeva M.I., Markovskaya E.F., Shibaeva T.G. Plants under continuous light: a review // Plant Stress. 2010. V. 4. P. 5–17.
- 4. Velez-Ramirez A.I., Van Ieperen W., Vreugdenhil D., Millenaar F.F. Plants under continuous light // Trends Plant Sci. 2011. V. 16. P. 310–318. https://doi.org/10.1016/j.tplants.2011.02.003
- 5. Shibaeva T.G., Titov A.F. Photoperiod stress in plants: a new look at plant response to abnormal light-dark cycles // Russ. J. Plant Physiol. 2025. V. 72:15. https://doi.org/10.1134/S102144372560165X
- 6. Shibaeva T.G., Sherudilo E.G., Rubaeva A.A., Titov A.F. Continuous LED lighting enhances yield and nutritional value of four genotypes of Brassicaceae microgreens // Plants. 2022. V. 11:176. https://doi.org/10.3390/plants11020176
- 7. Shibaeva T.G., Mamaev A.V., Titov A.F. Possible physiological mechanisms of leaf photodamage in plants grown under continuous lighting // Russ. J. Plant Physiol. 2023. V. 70:15. https://doi.org/10.1134/S1021443722602646
- 8. Шибаева Т.Г., Титов А.Ф. Всегда ли фотопериодический стресс вреден? // Труды КарНЦ РАН. Экспериментальная биология. 2025. № 5. С. 5–22. https://doi.org/10.17076/eb2098
- 9. Arthur J.W., Guthrie J.D., Newell J.M. Some effects of artificial climates on the growth and chemical composition of plants // Amer. J. Bot. 1930. V. 17. P. 416–482. https://doi.org/10.2307/2435930
- 10. Withrow A.P., Withrow R.B. Photoperiodic chlorosis in tomato // Plant Physiol. 1949. V. 24. P. 657–663. https://doi.org/10.1104/pp.24.4.657
- 11. Hillman W.S. Injury of tomato plants by continuous light and unfavorable photoperiodic cycles // Amer. J. Bot. 1956. V. 43. P. 89–96. https://doi.org/10.2307/2438816
- 12. Cushman K.E., Tibbitts T.W., Sharkey T.D., Wise R.R. Constant-light injury of potato: temporal and spatial patterns of carbon dioxide assimilation, starch content, chloroplast integrity, and necrotic lesions // J. Amer. Soc. Hort. Sci. 1995. V. 120. P. 1032–1040. https://doi.org/10.21273/JASHS.120.6.1032
- 13. Cushman K.E., Tibbitts T.W. The role of ethylene in the development of constant-light injury of potato and tomato // J. Amer. Soc. Hort. Sci. 1998. V. 123. P. 239–245. https://doi.org/10.21273/JASHS.123.2.239
- 14. Lim P.O., Kim H.J., Nam H.G. Leaf senescence // Annu. Rev. Plant Biol. 2007. V. 58. P. 115–136. https://doi.org/10.1146/annurev.arplant.57.032905.105316
- 15. Shibaeva T.G., Sherudilo E.G., Rubaeva A.A., Shmakova N.Y., Titov A.F. Response of native and non-native subarctic plant species to continuous illumination by natural and artificial light // Plants. 2024. V. 13:2742. https://doi.org/10.3390/plants13192742
- 16. Lichtenthaler H.K., Wellburn A.R. Determinations of total carotenoids and chlorophylls a and b of leaf extracts in different solvents // Biochem. Soc. Trans. 1983. V. 603. P. 591–592. https://doi.org/10.1042/bst0110591
- 17. Lichtenthaler H.K. Chlorophylls and carotenoids: pigment of photosynthetic biomembranes // Methods Enzymol. 1987. V. 148. P. 350–382. https://doi.org/10.1016/0076-6879 (87)48036-1
- 18. Kolupaev Y.E., Fisova E.N., Yastreb T.O., Ryabchun N.I., Kirichenko V.V. Effect of hydrogen sulfide donor on antioxidant state of wheat plants and their resistance to soil drought // Russ. J. Plant Physiol. 2019. V. 66. P. 59–66. https://doi.org/10.1134/S1021443719010084
- 19. Heath R.L., Packer L. Photoperioxidation in isolated chloroplasts I. Kinetics and stoichiometry of fatty acid peroxidation // Arch. Biochem. Biophys. 1968. V. 125. P. 189–198. https://doi.org/10.1016/0003-9861 (68)90654-1
- 20. Velikova V., Yordanov I., Edreva A. Oxidative stress and some antioxidant system in acid rain-treated bean plants: protective role of exogenous polyamines // Plant Sci. 2000. V. 151. P. 59–66. https://doi.org/10.1016/S0168-9452 (99)00197-1
- 21. Wheeler R.M. Potato and human exploration of space: some observations from NASA-sponsored controlled environment studies // Potato Res. 2006. V. 49. P. 67–90. https://doi.org/10.1007/s11540-006-9003-4
- 22. Murage E.N., Masuda M. Response of pepper and eggplant to continuous light in relation to leaf chlorosis and activities of antioxidative enzymes // Sci. Hort. 1997. V. 70. P. 269–279. https://doi.org/10.1016/s0304-4238 (97)00078-2
- 23. Dorais M., Gosselin A. Physiological response of greenhouse vegetable crops to supplemental lighting // Acta Hortic. 2002. V. 580. P. 59–67. https://doi.org/10.17660/ActaHortic.2002.580.6
- 24. Wolff S.A., Langerud A. Fruit yield, starch content and leaf chlorosis in cucumber exposed to continuous lighting // Eur. J. Hortic. Sci. 2006. V. 71. P. 259–261. https://doi.org/10.17660/eJHS.2006/173706
- 25. Haque M.S., Kjaer K.H., Rosenqvist E., Ottosen C.-O. Continuous light increases growth, daily carbon gain, antioxidants, and alters carbohydrate metabolism in a cultivated and a wild tomato species // Front. Plant Sci. 2015. V. 6:522. https://doi.org/10.3389/fpls.2015.00522
- 26. Velez-Ramirez A.I., van Ieperen W., Vreugdenhil D., van Poppel P.M., Heuvelink E., Millenaar F.F. The role of photosynthetic daily light integral in plant response to extended photoperiods // Russ. J. Plant Physiol. 2022. V. 69:7. https://doi.org/10.1134/s1021443722010216
- 27. Velez-Ramirez A.I., van Ieperen W., Vreugdenhil D., van Poppel P.M., Heuvelink E., Millenaar F.F. A single locus confers tolerance to continuous light and allows substantial yield increase in tomato // Nat. Commun. 2014. V. 5:4549. https://doi.org/10.1038/ncomms5549
- 28. Matsuda R., Ozawa N., Fujiwara K. Leaf photosynthesis, plant growth, and carbohydrate accumulation of tomato under different photoperiods and diurnal temperature differences // Sci. Hortic. 2014. V. 170. P. 150–158. https://doi.org/10.1016/j.scienta.2014.03.014
- 29. Pham M.D., Hwang H., Park S.W., Cui M., Lee H., Chun C. Leaf chlorosis, epinasty, carbohydrate contents and growth of tomato show different responses to the red/blue wavelength ratio under continuous light // Plant Physiol. Biochem. 2019. V. 141. P. 477–486. https://doi.org/10.1016/j.plaphy.2019.06.004
- 30. Foyer C.H., Neukermans J., Queval G., Noctor G., Harbinson J. Photosynthetic control of electron transport and the regulation of gene expression // J. Exp. Bot. 2012. V. 63. P. 1637–1661. https://doi.org/10.1093/jxb/ers013
- 31. Zhu M.-D., Chen X.-L., Zhu X.-Y., Xing Y.-D., Du D., Zhang Y.-Y., Liu M.-M., Zhang Q.-L., Lu X., Peng S.-S., He G.-H., Zhang T.-Q. Identification and gene mapping of the starch accumulation and premature leaf senescence mutant ossac4 in rice // J. Integr. Agric. 2020. V. 19. P. 2150–2164. https://doi.org/10.1016/S2095-3119 (19)62814-5
- 32. Pammenter N.W., Loreto F., Sharkey T.D. End product feedback effects on photosynthetic electron transport // Photosynth. Res. 1993. V. 35. P. 5–14. https://doi.org/10.1007/BF02185407
- 33. Van Gestel N.C., Nesbit A.D., Gordon E.P., Green C., Paré P.W., Thompson L., Peffley E.B., Tissue D.T. Continuous light may induce photosynthetic downregulation in onion — consequences for growth and biomass partitioning // Physiol. Plant. 2005. V. 125. P. 235–246. https://doi.org/10.1111/j.1399-3054.2005.00560.x
- 34. Smith A.M., Stitt M. Coordination of carbon supply and plant growth // Plant Cell Environ. 2007. V. 30. P. 1126–1149. https://doi.org/10.1111/j.1365-3040.2007.01708.x
- 35. Fischer A.M. The complex regulation of senescence // Crit. Rev. Plant Sci. 2012. V. 31. P. 124–147. https://doi.org/10.1080/07352689.2011.616065
- 36. Thomas H. Senescence, ageing and death of the whole plant // New Phytol. 2013. V. 197. P. 696–711. https://doi.org/10.1111/nph.12047
- 37. Swartzberg D., Hanael R., Granot D. Relationship between hexokinase and cytokinin in the regulation of leaf senescence and seed germination // Plant Biol. 2011. V. 13. P. 439–444. https://doi.org/10.1111/j.1438-8677.2010.00376.x
- 38. Roeber V.M., Bajaj I., Rohde M., Schmulling T., Cortleven A. Light acts as a stressor and influences abiotic and biotic stress responses in plants // Plant Cell Environ. 2021. V. 44:645. https://doi.org/10.1111/pce.13948
- 39. Roeber V.M., Schmülling T., Cortleven A. The photoperiod: handling and causing stress in plants // Front. Plant Sci. 2022. V. 12:781988. https://doi.org/10.3389/fpls.2021.781988
- 40. Haque M.S., Kjaer K.H., Rosenqvist E., Ottosen C.-O. Recovery of tomato (Solanum lycopersicum L.) leaves form continuous light induced injury // J. Plant Physiol. 2015. V. 185. P. 24–30. https://doi.org/10.1016/j.jplph.2015.06.011