Physiological responses of microclonally propagated willow to excessive levels of UV-B radiation
Abstract
Willow plantations represent a rapidly deployable source of lignocellulosic biomass for bioenergy and a reservoir of bioa c tive compounds for pharmaceutical use. However, their physiological resilience to increasing ultraviolet-B (UV-B; radiation with a wavelength of 280–320 nm), under current climate change scenarios, remains insufficiently characterised. This study evaluated the physiological responses of the microclonally propagated willow clone ‘Zhytomyrska-1’ to acute UV-B treatments. Our exp e riments were focused on leaf pigmentation and nitrogen-related status as indicators of stress. Uniform in vitro -derived plantlets were acclimatised in greenhouse conditions and divided into four groups: non-irradiated control and three UV-B treatments r e ceiving single acute doses of 5, 10, and 15 kJ/m². Non-destructive leaf measurements were performed with a portable multipi g ment meter (MPM-100) at seven time points during a two-month period post-exposure to capture short-, medium- and long-term effects. We determined relative chlorophyll, flavonol, and anthocyanin indices, and the nitrogen balance index (NBI) as an int e grative parameter for leaf nitrogen status. Data were analysed by both one-way and two-way ANOVA to separate the effects of dose, time and their interaction. Time (developmental stage and seasonal progression) was the dominant factor driving variation in all measured parameters, excluding anthocyanin. The contents of chlorophyll and flavonol were increased at later stages of the vegetation, on days 66 and 70. Meanwhile, the nitrogen balance index tended to decrease at the time points 10–17 days, but this effect was absent after UV-B ir radiation at 15 kJ/m², where the nitrogen balance index remained relatively stable during the st u died period. Compared to the impact of time, the effects of UV-B radiation were weaker and less consistent, in some cases i n creasing the levels of chlorophyll and the nitrogen balance index, while decreasing th e levels of anthocyanins. Overall, the willow clone ‘Zhytomyrska-1’ demonstrated relative physiological stability across the tested UV-B dose range, suggesting resilience to mo d erate increases in UV-B comparable to regional annual doses.References
Ali, A., Santoro, P., Mori, J., Ferrante A., & Cocetta, G. (2024). Effect of UV-B elicitation on spearmint’s (Mentha spicata L.) morpho-physiological traits and secondary metabolites production. Plant Growth Regulations, 104, 63–76.
Amichev, B. Y., Hangs, R. D., Konecsni, S. M., Stadnyk, C. N., Volk, T. A., Bélanger, N., Vujanovic, V., Schoenau, J. J., Moukoumi, J., & Van Rees, K. C. J. (2014). Willow short-rotation production systems in Canada and Northern United States: A review. Soil Science Society of America Journal, 78(1), 168–182.
Cerovic, Z. G., Moise, N., Agati, G., Latouche, G., Ben Ghozlen, N., & Meyer, S. (2008). New portable optical sensors for the assessment of winegrape phenolic maturity based on berry fluorescence. Journal of Food Composition and Analysis, 21(8), 650–654.
Czégény, G., Mátai, A., & Hideg, É. (2016). UV-B effects on leaves – oxidative stress and acclimation in controlled environments. Plant Science, 248, 57–63.
Dimitriou, I., & Mola-Yudego, B. (2017). Poplar and willow plantations on agricultural land in Sweden: Area, yield, groundwater quality and soil organic carbon. Forest Ecology and Management, 383, 99–107.
Dou, J., Galvis, L., Holopainen-Mantila, U., Reza, M., Tamminen, T., & Vuorinen, T. (2016). Morphology and overall chemical characterization of willow (Salix sp.) inner bark and wood: Toward controlled deconstruction of willow biomass. ACS Sustainable Chemistry and Engineering, 4(7), 3871–3876.
Fang, X., Pyle, J. A., Chipperfield, M. P., Daniel, J. S., Park, S., & Prinn, R. G. (2019). Challenges for the recovery of the ozone layer. Nature Geoscience, 12, 592–596.
Hangs, R. D., Schoenau, J. J., Van Rees, K. C. J., & Steppuhn, H. (2011). Examining the salt tolerance of willow (Salix spp.) bioenergy species for use on salt-affected agricultural lands. Canadian Journal of Plant Science, 91(3), 509–517.
Holoborodko, K. K., Sytnyk, S. A., Lovynska, V. M., Ivanko, I. A., Loza, I. M., & Brygadyrenko, V. V. (2022). Impact of invasive species Parectopa robiniella (Gracillariidae) on fluorescence parameters of Robinia pseudoacacia in the conditions of the steppe zone of Ukraine. Regulatory Mechanisms in Biosystems, 13(3), 324–330.
Hu, Z., Li, H., Chen, S., & Yang, Y. (2013). Chlorophyll content and photosystem II efficiency in soybean exposed to supplemental ultraviolet-B radiation. Photosynthetica, 51(1), 151–157.
Hui, R., Li, X., Chen, C., Zhao, X., Jia, R., Liu, L., & Wei, Y. (2012). Responses of photosynthetic properties and chloroplast ultrastructure of Bryum argenteum from a desert biological soil crust to elevated ultraviolet-B radiation. Physiologia Plantarum, 147(4), 489–501.
Jadidi, M., Mumivand, H., Ehtesham Nia, A., Shayganfar, A., & Maggi, F. (2023). UV-A and UV-B combined with photosynthetically active radiation change plant growth, antioxidant capacity and essential oil composition of Pelargonium graveolens. BMC Plant Biology, 23, 555.
Jansen, M. A. K., Gaba, V., & Greenberg, B. M. (1998). Higher plants and UV B radiation: Balancing damage, repair and acclimation. Trends in Plant Science, 3(4), 131–135.
Kaling, M., Kanawati, B., Ghirardo, A., Albert, A., Winkler, J. B., Heller, W., Barta, C., Loreto, F., Schmitt-Kopplin, P., & Schnitzler, J.-P. (2014). UV-B mediated metabolic rearrangements in poplar revealed by non-targeted metabolomics. Plant, Cell and Environment, 38(5), 892–904.
Kameoka, S., Isoda, S., Hashimoto, A., Ito, R., Miyamoto, S., Wada, G., Watanabe, N., Yamakami, T., Suzuki, K., & Kameoka, T. (2017). A wireless sensor network for growth environment measurement and multi-band optical sensing to diagnose tree vigor. Sensors, 17(5), 966.
Kataria, S., Jajoo, A., & Guruprasad, K. N. (2014). Impact of increasing ultraviolet-B (UV-B) radiation on photosynthetic processes. Journal of Photochemistry and Photobiology B: Biology, 137, 55–66.
Khoma, Y. A., Nesterenko, O. G., Kutsokon, N. K., Khudolieieva, L. V., Shevchenko, V. V., & Rashydov, N. M. (2021). Proline content in the leaves of poplar and willow under water deficit. Regulatory Mechanisms in Biosystems, 12(3), 519–522.
Kutsokon, N., & Khoma, Y. (2025). Effects of drought stress on spring bud development in poplar and willow clones. Dendrobiology, 93, 86–97.
Kutsokon, N., Rakhmetov, D., Rakhmetova, S., Khudolieieva, L., & Rashydov, N. (2022). Nursery screening of poplar and willow clones for biofuel application in Ukraine. iForest: Biogeosciences and Forestry, 15(5), 401–410.
León-Chan, R. G., López-Meyer, M., Osuna-Enciso, T., Sañudo-Barajas, J. A., Heredia, J. B., & León-Félix, J. (2017). Low temperature and ultraviolet-B radiation affect chlorophyll content and induce the accumulation of UV-B-absorbing and antioxidant compounds in bell pepper (Capsicum annuum) plants. Environmental and Experimental Botany, 139, 143–151.
Lidon, F. C., & Ramalho, J. C. (2011). Impact of UV-B irradiation on photosynthetic performance and chloroplast membrane components in Oryza sativa L. Journal of Photochemistry and Photobiology B: Biology, 104(3), 457–466.
Liu, W., & Jenkins, G. I. (2024). Recent advances in UV-B signalling: Interaction of proteins with the UVR8 photoreceptor. Journal of Experimental Botany, 76(3), 873–881.
Nassour, R., & Ayash, A. (2021). Effects of ultraviolet B radiation in plant physiology. Agriculture, 67(1), 1–15.
Rai, K., & Agrawal, S. B. (2017). Effects of UV-B radiation on morphological, physiological and biochemical aspects of plants: An overview. Journal of Scientific Research, 61, 87–113.
Rakhmetov, D., Bondarchuk, O., Rakhmetova, S., Blume, Y., Blume, R., Kutsokon, N., & Rashydov, N. (2024). Physiological state of Brassica carinata plants depending on genotype characteristics and phase of plant development in the conditions of Kyiv. In: Andronic, L., & Brindza, J. (Eds.). Proceedings of the International Scientific Conference “Genetics, Physiology and Plant Breeding”. Moldova State University, Chisinau. Pp. 180–184.
Randriamanana, T. R., Nissinen, K., Moilanen, J., Nybakken, L., & Julkunen-Tiitto, R. (2015). Long-term UV-B and temperature enhancements suggest that females of Salix myrsinifolia plants are more tolerant to UV-B than males. Environmental and Experimental Botany, 109, 296–305.
Reisz, J. A., Bansal, N., Qian, J., Zhao, W., & Furdui, C. M. (2014). Effects of ionizing radiation on biological molecules – mechanisms of damage and emerging methods of detection. Antioxidants and Redox Signaling, 21(2), 260–292.
Ren, J., Duan, B., Zhang, X., Korpelainen, H., & Li, C. (2010). Differences in growth and physiological traits of two poplars originating from different altitudes as affected by UV-B radiation and nutrient availability. Physiologia Plantarum, 138(3), 278–288.
Salama, H. M. H., Al Watban, A. A., & Al-Fughom, A. T. (2011). Effect of ultraviolet radiation on chlorophyll, carotenoid, protein and proline contents of some annual desert plants. Saudi Journal of Biological Sciences, 18(1), 79–86.
Singh, S., Kumari, R., Agrawal, M., & Agrawal, S. B. (2012). Differential response of radish plants to supplemental ultraviolet-B radiation under varying NPK levels: Chlorophyll fluorescence, gas exchange and antioxidants. Physiologia Plantarum, 145(3), 474–484.
Solomon, S. (2020). Risks to the stratospheric ozone shield in the Anthropocene. Ambio, 50, 44–48.
Stolarski, M. J., Szczukowski, S., Tworkowski, J., Klasa, A., & Wróblewska, H. (2013). Yield, energy parameters and chemical composition of short-rotation willow biomass. Industrial Crops and Products, 46, 60–65.
Van Slycken, S., Witters, N., Meiresonne, L., Meers, E., Ruttens, A., Van Peteghem, P., Weyens, N., Tack, F. M. G., & Vangronsveld, J. (2012). Field evaluation of willow under short rotation coppice for phytomanagement of metal-polluted agricultural soils. International Journal of Phytoremediation, 15(7), 677–689.
Volk, T. A., Heavey, J. P., & Eisenbies, M. H. (2016). Advances in shrub-willow crops for bioenergy, renewable products, and environmental benefits. Food and Energy Security, 5(2), 97–106.
Wang, G., Hao, Z., Anken, R. H., Lu, J., & Liu, Y. (2010). Effects of UV-B radiation on photosynthesis activity of Wolffia arrhiza as probed by chlorophyll fluorescence transients. Advances in Space Research, 45(7), 839–845.
Wong, T. M., Sullivan, J. H., & Eisenstein, E. (2022). Acclimation and compensating metabolite responses to UV-B radiation in natural and transgenic Populus spp. defective in lignin biosynthesis. Metabolites, 12(8), 767.
Yao, X., Jianzhou, C., Xueli, H., Binbin, L., Jingmin, L., & Zhaowei, Y. (2013). Effects of selenium on agronomical characters of winter wheat exposed to enhanced ultraviolet-B. Ecotoxicology and Environmental Safety, 92, 320–326.
Zhao, Q. Z., Dong, M. Y., Li, M. F., Jin, L., & Pare, P. W. (2023). Light-induced flavonoid biosynthesis in Sinopodophyllum hexandrum with high-altitude adaptation. Plants, 12(3), 575.
Zlatev, Z. S., Lidon, F. C., & Kaimakanova, M. (2012). Plant physiological responses to UV-B radiation. Emirates Journal of Food and Agriculture, 24(6), 529–540.
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