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Enhancing drought resilience in Persian walnut genotypes: Insights from photosynthetic dynamics and phenotypic analysis | ||
| Journal of Plant Physiology and Breeding | ||
| دوره 15، شماره 2، 2025، صفحه 355-372 اصل مقاله (893.45 K) | ||
| نوع مقاله: Research Paper | ||
| شناسه دیجیتال (DOI): 10.22034/jppb.2025.68929.1376 | ||
| نویسندگان | ||
| Hojjat Ataee1؛ Mahdi Alizadeh* 2؛ Saadat Sarikhani3؛ Kourosh Vahdati3 | ||
| 1Department of Horticulture, Gorgan University of Agricultural Sciences and Natural Resources, Gorgan, Iran; Department of Horticulture, College of Aburaihan, University of Tehran, Tehran, Iran. | ||
| 2Department of Horticulture, Gorgan University of Agricultural Sciences and Natural Resources, Gorgan, Iran. | ||
| 3Department of Horticulture, College of Aburaihan, University of Tehran, Tehran, Iran. | ||
| چکیده | ||
| Objective: The Persian walnut (Juglans regia L.), known for its notable sensitivity to drought stress, exhibits considerable genetic diversity within Iran. This genetic variability provides a valuable resource for developing and selecting drought-tolerant rootstocks. Methods: This study investigates the effects of water withholding on 115 walnut families from various climatic zones in Khorasan Razavi province, Iran, by analyzing polyphasic fast chlorophyll a fluorescence induction (OJIP), relative water content (RWC), and chlorophyll index (SPAD). Results: We observed reductions in electron transport flux per reaction center (ET0/RC), relative maximal variable fluorescence (FM/F0), maximum quantum efficiency of PSII (FV/FM), quantum yield of electron transport (Phi-E0), and the performance index (PI-ABS) in response to drought stress. In contrast, increases were observed in dissipated energy flux (DI0/RC), quantum yield of energy dissipation (Phi-D0), and specific energy fluxes per reaction center for energy absorption (ABS/RC), which are associated with photo-inhibition in plants subjected to water withholding. Using drought tolerance assessments and principal component analysis, we tentatively categorized the 115 walnut families into sensitive, tolerant, and moderately tolerant groups. Tolerant families, such as G107, B31, B66, B68, and B142, exhibited less variation in most traits from normal to drought-stress conditions, compared to sensitive and moderately tolerant families. Conclusion: Our findings highlight the effectiveness of chlorophyll fluorescence characteristics, RWC, and SPAD for the rapid identification of drought-tolerant genotypes. | ||
| کلیدواژهها | ||
| Drought stress؛ Drought tolerance؛ Native population؛ OJIP test؛ Walnut | ||
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| مراجع | ||
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Adhikari KN, Buirchell BJ, Thomas GJ, Sweetingham MW, Yang H. 2009. Identification of anthracnose resistance in Lupinus albus L. and its transfer from landraces to modern cultivars. Crop Pasture Sci. 60: 472–479. http://dx.doi.org/10.1071/CP08092
Aletà N, Vilanova, A, Díaz R, Voltas J. 2009. Genetic variation for carbon isotope composition in Juglans regia L.: Relationships with growth, phenology and climate of origin. Ann For Sci. 66(4): 413. https://doi.org/10.1051/forest/2009021
Aliniaeifard S, Van Meeteren U. 2016a. Stomatal characteristics and desiccation response of leaves of cut chrysanthemum (Chrysanthemum morifolium) flowers grown at high air humidity. Sci Hortic. 205: 84–89. https://doi.org/10.1016/j.scienta.2016.04.025
Aliniaeifard S, Van Meeteren U. 2016b. Natural genetic variation in stomatal response can help to increase acclimation of plants to dry environments. In: International Symposium on the Role of Plant Genetic Resources in Reclaiming Lands and Environment Deteriorated by Human and Natural Actions. 1190: 71–76. https://doi.org/10.17660/ActaHortic.2018.1190.12
Arab MM, Marrano A, Abdollahi-Arpanahi R, Leslie CA, Cheng H, Neale DB, Vahdati K. 2020. Combining phenotype, genotype, and environment to uncover genetic components underlying water use efficiency in Persian walnut. J Exp Bot. 71(3): 1107–1127. https://doi.org/10.1093/jxb/erz467
Arab MM, Askari H, Aliniaeifard S, Mokhtassi-Bidgoli A, Estaji A, Sadat-Hosseini M, Sohrabi SS, Mesgaran MB, Leslie CA, Brown PJ, et al. 2023. Natural variation in photosynthesis and water use efficiency of locally adapted Persian walnut populations under drought stress and recovery. Plant Physiol Biochem. 201: 107859. https://doi.org/10.1016/j.plaphy.2023.107859
Athar H-u-R, Ambreen S, Javed M, Hina M, Rasul S, Zafar ZU, Manzoor H, Ogbaga CC, Afzal M, Al-Qurainy F, et al. 2016. Influence of sub-lethal crude oil concentration on growth, water relations and photosynthetic capacity of maize (Zea mays L.) plants. Environ Sci Pollut Res. 23: 18320–18331. https//doi.org/10.1007/s11356-016-6976-7
Bano H, Athar HU, Zafar ZU, Kalaji HM, Ashraf M. 2021. Linking changes in chlorophyll a fluorescence with drought stress susceptibility in mung bean [Vigna radiata (L.) Wilczek]. Physiol Plant. 172(2): 1244–1254. https://doi.org/10.1111/ppl.13327
Behzadi Rad P, Roozban MR, Karimi S, Ghahremani R, Vahdati K. 2021. Osmolyte accumulation and sodium compartmentation has a key role in salinity tolerance of pistachio rootstocks. Agriculture. 11(8): 708. https://doi.org/10.3390/agriculture11080708
Bresson J, Vasseur F, Dauzat M, Koch G, Granier C, Vile D. 2015. Quantifying spatial heterogeneity of chlorophyll fluorescence during plant growth and in response to water stress. Plant Methods. 11: 23. https://doi.org/10.1186/s13007-015-0067-5
Çiçek N, Pekcan V, Arslan Ö. 2019. Assessing drought tolerance in field-grown sunflower hybrids by chlorophyll fluorescence kinetics. Braz J Bot. 42: 249–260. http://doi.org/10.1007s40415-019-00534-1
Demmig-Adams B, Stewart J, Baker C, Adams W. 2018. Optimization of photosynthetic productivity in contrasting environments by regulons controlling plant form and function. Int J Mol Sci. 19: 872. https://doi.org/10.3390/ijms19030872
Dong Z, Men Y, Liu Z, Li J, Ji J. 2020. Application of chlorophyll fluorescence imaging technique in analysis and detection of chilling injury of tomato seedlings. Comput Electron Agric. 168: 105109. https://doi.org/10.1016/j.compag.2019.105109
Fahimi Khoyerdi F, Shamshiri MH, Estaji A. 2016. Changes in some physiological and osmotic parameters of several pistachio genotypes under drought stress. Sci Hortic. 198: 44–51. http://10.1016/j.scienta.2015.11.028
Guellim A, Hirel B, Chabrerie O. 2020. Screening for durum wheat (Triticum durum Desf.) cultivar resistance to drought stress using an integrated physiological approach. J Crop Sci Biotechnol. 23: 355–365. https://doi.org/10.1007/s12892-020-00043-8
Hu F, Zhang Y, Guo J. 2023. Effects of drought stress on photosynthetic physiological characteristics, leaf microstructure, and related gene expression of yellow horn. Plant Signal Behav. 18:1. https://doi.org/10.1080/15592324.2023.2215025
Kalaji HM, Jajoo A, Oukarroum A, Brestic M, Zivcak M, Samborska IA, Cetner MD, Łukasik I, Goltsev V, Ladle RJ. 2016. Chlorophyll a fluorescence as a tool to monitor physiological status of plants under abiotic stress conditions. Acta Physiol. Plant. 38(4): 102. https://doi.org/10.1007/s11738-016-2113-y
Karimi S, Yadollahi A, Arzani K, Imani A, Aghaalikhani M. 2015. Gas-exchange response of almond genotypes to water stress. Photosynthetica. 53(1): 29–34. https://doi.org/10.1007/s11099-015-0070-0
Kassambara A, Mundt F. 2017. Factoextra: Extract and visualize the results of multivariate data analyses. R Package Version 1.0.7. Available at: https://cran.r-project. org/web/packages/factoextra/index.html (Accessed 4 October 2022).
Küpper H, Benedikty Z, Morina F, Andresen E, Mishra A, Trtílek M. 2019. Analysis of OJIP chlorophyll fluorescence kinetics and QA reoxidation kinetics by direct fast imaging. Plant Physiol. 179(2): 369-381. https://doi.org/10.1104/pp.18.00953
Liu B, Cheng L, Liang D, Zou Y, Ma F. 2012. Growth, gas exchange, water-use efficiency, and carbon isotope composition of ‘Gale Gala’ apple trees grafted onto 9 wild Chinese rootstocks in response to drought stress. Photosynthetica. 50(3): 401–410. https://doi.org/10.1007/s11099-012-0048-0
Mafakheri A, Siosemardeh A, Bahramnejad B, Struik PC, Sohrabi E. 2010. Effect of drought stress on yield, proline and chlorophyll contents in three chickpea cultivars. Aust J Crop Sci. 4: 580–585.
Mathur S, Mehta P, Jajoo A. 2013. Effects of dual stress (high salt and high temperature) on the photochemical efficiency of wheat leaves (Triticum aestivum). Physiol Mol Biol. 19(2): 179–188. https://doi.org/10.1007/s12298-012-0151-5
Sharma DK, Andersen SB, Ottosen CO, Rosenqvist E. 2015. Wheat cultivars selected for high Fv/Fm under heat stress maintain high photosynthesis, total chlorophyll, stomatal conductance, transpiration and dry matter. Physiol Plant. 153: 284–298. https://doi.org/10.1111/ppl.12245
Sousaraei N, Mashayekhi K, Mousavizadeh SJ, et al. 2021. Screening of tomato landraces for drought tolerance based on growth and chlorophyll fluorescence analyses. Hortic Environ Biotechnol. 62: 521–535. https://doi.org/10.1007/s13580-020-00328-5
Strasser RJ, Srivastava A, Tsimilli-Michael M. 2000. The fluorescence transient as a tool to characterize and screen photosynthetic samples. In: Yunus M (ed.) Probing Photosynthesis: Mechanisms, Regulation and Adaptation. London: Taylor and Francis, pp. 445-483.
Strasser RJ, Tsimilli-Michael M, Srivastava A. 2004. Analysis of the chlorophyll a fluorescence transient. In: Papageorgiou GC (ed.) Chlorophyll a Fluorescence. Netherlands: Springer, pp. 321–362. https://doi.org/10.1007/978-1-4020-3218-9_12
Su L, Dai Z, Li S, Xin H. 2015. A novel system for evaluating drought–cold tolerance of grapevines using chlorophyll fluorescence. BMC Plant Biol. 15: 82. https://doi.org/10.1186/s12870-015-0459-8
Tomášková I, Pastierovič F, Krejzková A, Čepl J, Hradecký J. 2021. Norway spruce ecotypes distinguished by chlorophyll a fluorescence kinetics. Acta Physiol Plant. 43: 24. https://doi.org/10.1007/s11738-020-03190-1
Vahdati K, Sarikhani Khorami S, Arab M. 2018. Walnut: A potential multipurpose nut crop for reclaiming deteriorated lands and environment. Acta Hortic. 1190: 95–100. https://doi.org/10.17660/ActaHortic.2018.1190.16
Vahdati K, Arab MM, Sarikhani S. 2020. Advances in biotechnology and propagation of nut trees in Iran. BIO Web of Conferences. EDP Sciences 25: 01003. https://doi.org/10.1051/bioconf/20202501003
Viljevac Vuletić M, Horvat D, Mihaljević I, Dugalić K, Šimić D, Čupić T, Jurković V, Lepeduš H. 2022. Photosynthetic variability of Oblačinska sour cherry ecotypes under drought. Plants. 11: 1764. https://doi.org/10.3390/plants11131764
Wang X, Wu J, Yang Z, Zhang F, Sun H, Qiu X, Yi F, Yang D, Shi F. 2019. Physiological responses and transcriptome analysis of the Kochia prostrata (L.) Schrad. to seedling drought stress. AIMS Genet. 6(2): 17-35. https://doi.org/10.3934/genet.2019.2.17
Wójcik-Jagła M, Rapacz M, Tyrka M, Janusz Kościelniak J, Crissy K, Zmuda K. 2013. Comparative QTL analysis of early short-time drought tolerance in Polish fodder and malting spring barleys. Theor Appl Genet. 126(12): 3021–3034. https://doi.org/10.1007/s00122-013-2190-x
Xiao X, Xu X, Yang F. 2008. Adaptive responses to progressive drought stress in two Populus cathayana populations. Silva Fenn. 42(5): 705–719. https://doi.org/10.14214/sf.224
Xu Z, Zhou G. 2008. Responses of leaf stomatal density to water status and its relationship with photosynthesis in a grass. J Exp Bot. 59(12): 3317–3325. https://doi.org/10.1093/jxb/ern185
Zhou R, Yu X, Kjær KH, Rosenqvist E, Ottosen CO, Wu Z. 2015. Screening and validation of tomato genotypes under heat stress using Fv/Fm to reveal the physiological mechanism of heat tolerance. Environ Exp Bot. 118: 1–11. https://doi.org/10.1016/j.envexpbot.2015.05.006
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