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Estimating the Morphological and Physiological Plasticity of Ligustrum obtusifolium Seedlings in Response to Drought Stress and Subsequent Rewatering

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Abstract

Drought resistance and post drought recovery strategy and ability are important parameters to measure adaptation of plants to heterogeneous water environments; in addition, they are very important to study costs and benefits of plasticity. We compared the differences in multiple traits of Ligustrum obtusifolium seedlings under four water conditions, well-watered, light drought, moderate drought, and severe drought, for 30 days, as well as under rewatering conditions for 7, 14, and 21 days in the greenhouse. We observed increased levels of malondialdehyde content, antioxidant activity, and osmotic adjustment substances and significantly decreased stem height, leaf area, specific leaf area, aboveground biomass, total biomass, and chlorophyll content in response to drought stress. The root biomass and root–shoot ratio reached maximum values under moderate drought conditions. The seedlings subjected to light and moderate drought recorded physiological parameters that were similar to control levels after 21 days of rewatering. However, the seedlings under severe drought treatment did not show such recovery and only carotenoids content returned to the control levels. In conclusion, the extent of plants recovery after rewatering depends on drought stress severity and rewatering time. The early drought experience may not be harmful immediately, but it can induce active biochemical responses, to support morphological, biomass, and photosynthetic physiological traits responses under subsequent rewatering.

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References

  • Abid M, Tian Z, Ata-Ul-Karim ST et al (2016) Adaptation to and recovery from drought stress at vegetative stages in wheat (Triticum aestivum) cultivars. Funct Plant Biol 43:1159–1169

    Article  CAS  PubMed  Google Scholar 

  • Acharya A, Pesacreta TC (2023) P-ring: the conserved nature of phosphorus enriched cells in seedling roots of distantly related species. Plant Signal Behav 18:2217389

    Article  PubMed  PubMed Central  Google Scholar 

  • Ackermann M (2015) Afunctional perspective on phenotypic heterogeneity in microorganisms. Nat Rev Microbiol 13:497–508

    Article  CAS  PubMed  Google Scholar 

  • Agrawal AA (2000) Overcompensation of plants in response to herbivory and the by-product benefits of mutualism. Trends Plant Sci 5:309–313

    Article  CAS  PubMed  Google Scholar 

  • Aidar ST, Meirelles ST, Oliveira RF et al (2014) Photosynthetic response of poikilochlorophyllous desiccation-tolerant Pleurostima purpurea (Velloziaceae) to dehydration and rewatering. Photosynthetica 52:124–133

    Article  CAS  Google Scholar 

  • Ammar A, Aissa IB, Mars M et al (2020) Comparative physiological behavior of fig (Ficus carica L) cultivars in response to water stress and recovery. Sci Hortic 260:108881

    Article  CAS  Google Scholar 

  • Balakhnina T, Gins M, Fomina I (2019) Oxidative stress development in the leaves of Amaranthus cruentus L. containing amaranthine under conditions of nighttime low temperatures, soil hypoxia and the combined effects of both stress factors. Int Agrophys 33:511–516

    Article  CAS  Google Scholar 

  • Baquedano FJ, Valladares F, Castillo FJ (2008) Phenotypic plasticity blurs ecotypic divergence in the response of Quercus coccifera and Pinus halepensis to water stress. Eur J Forest Res 127:495–506

    Article  Google Scholar 

  • Blokhina O, Virolainen E, Fagerstedt KV (2003) Antioxidants, oxidative damage and oxygen deprivation stress: a review. Ann Bot 91:179–194

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Blum A (1996) Crop responses to drought and the interpretation of adaptation. Plant Growth Regul 20:135–148

    Article  CAS  Google Scholar 

  • Cai Y (2014) Guidance of plant physiology experiments. China Agriculture University, Beijing, pp 121–129

    Google Scholar 

  • Cai YF, Wang JH, Zhang L et al (2019) Physiological and transcriptomic analysis highlight key metabolic pathways in relation to drought tolerance in Rhododendron delavayi. Physiol Mol Biol Pla 25:991–1008

    Article  CAS  Google Scholar 

  • Chai CR (2010) An analysis on moisture suitibility of six landscape shrubs species in Northern China. Northeast Forestry Univ

    Google Scholar 

  • Chang YC (2012) The impact of anatomical structure for 9 kinds of plants at stress of drought and automobile exhaust. Northeast Forestry Univ

    Google Scholar 

  • Chen S, Lin G, Huang J et al (2010) Dependence of carbon sequestration on the differential responses of ecosystem photosynthesis and respiration to rain pulses in a semiarid steppe. Global Change Biol 15:2450–2461

    Article  Google Scholar 

  • Doupis PG, Kavroulakis N, Psarras G et al (2017) Growth, photosynthetic performance and antioxidative response of “Hass” and “Fuerte” avocado (Persea americana Mill) plants grown under high soil moisture. Photosynthetica: Int J Photosynth Res 55:655–663

    Article  CAS  Google Scholar 

  • Du N, Guo W, Zhang X et al (2010) Morphological and physiological responses of Vitex negundo L. var. heterophylla (Franch.) Rehd. to drought stress. Acta Physiol Plant 32:839–848

    Article  Google Scholar 

  • Gao J (2006) Experimental guidance of plant physiology. Higher Education, Beijing, pp 76–78

    Google Scholar 

  • Gao J, Cai Y (2018) Experimental guidance of plant physiology. China Agriculture University, Beijing, pp 98–101

    Google Scholar 

  • Gong MM, Zhang RY, Liu Y et al (2022) Effects of drought stress on growth and root antioxidant enzymes activities in red raspberry seedlings. Nonwood Forest Res 40:232–240

    Google Scholar 

  • Hasanuzzaman M, Bhuyan M, Zulfiqar F et al (2020) Reactive oxygen species and antioxidant defense in plants under abiotic stress: revisiting the crucial role of a universal defense regulator. Antioxidants 9:681

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Hendry AP (2016) Key questions on the role of phenotypic plasticity in eco-evolutionary dynamics. J Hered 107:25–41

    Article  PubMed  Google Scholar 

  • Herzog M, Striker GG, Colmer TD et al (2017) Mechanisms of waterlogging tolerance in wheat, a review of root and shoot physiology. Plant Cell Environ 39:1068–1086

    Article  Google Scholar 

  • Hirabayashi Y, Mahendran R, Koirala S et al (2013) Global flood risk under climate change. Nat Clim Change 3:816–821

    Article  Google Scholar 

  • Huang J, Yu H, Guan X et al (2016) Accelerated dryland expansion under climate change. Nat Clim Change 6:166–172

    Article  Google Scholar 

  • Huber H, Chen X, Hendriks M et al (2012) Plasticity as a plastic response: how submergence induced leaf elongation in Rumex palustris depends on light and nutrient availability in its early life stage. New Phytol 194:572–582

    Article  PubMed  Google Scholar 

  • Izanloo A, Condon AG, Langridge P et al (2008) Different mechanisms of adaptation to cyclic water stress in two South Australian bread wheat cultivars. J Exp Bot 59:3327–3346

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Jackson RB, Sperry JS, Dawson TE (2000) Root water uptake and transport: using physiological processes in global predictions. Trend Plant Sci 5:482–488

    Article  CAS  Google Scholar 

  • Jia Y, Xiao W, Ye Y et al (2020) Response of photosynthetic performance to drought duration and re-watering in Maize. Agronomy 10:533

    Article  Google Scholar 

  • Li HS (2000) Experimental principles and techniques of plant physiology and biochemistry. Higher Education, Beijing, pp 134–200

    Google Scholar 

  • Li R, Wang YJ, He CG et al (2015) Effect of drought and heat stress on morphology and photosynthetic pigment contents of Medicago sativa. Grassland Turf 35:37–43

    Google Scholar 

  • Lichtenthaler HK (1987) Chlorophylls and carotenoids: pigments of photosynthetic biomembranes. Method Enzymol 148:350–382

    Article  CAS  Google Scholar 

  • Liu TT, Chen DQ, Wang SW et al (2018) Physiological and ecological responses of different varieties of sorghum seedlings during drought and rehydration. Acta Pratensis 27:100–110

    Google Scholar 

  • Lopes MS, Luis AJ, Van HPDR et al (2011) Enhancing drought tolerance in C4 crops. J Exp Bot 62:3135–3153

    Article  CAS  PubMed  Google Scholar 

  • Lu Q, Xu J, Fu X et al (2019) Physiological and growth responses of two dogwoods to short-term drought stress and re-watering. Acta Ecol Sinica 40:172–177

    Article  Google Scholar 

  • Manivannan P, Abdul JC, Sankar B et al (2007) Growth, biochemical modifications and proline metabolism in Helianthus annuus L. as induced by drought stress. Colloid Surface B 59:141–149

    Article  CAS  Google Scholar 

  • Marchiori PER, Machado EC, Sales CRG et al (2017) Physiological plasticity is important for maintaining sugarcane growth under water deficit. Front Plant Sci 8:02148

    Article  Google Scholar 

  • Miller G, Suzuki N, Ciftci-Yilmaz S et al (2010) Reactive oxygen species homeostasis and signaling during drought and salinity stresses. Plant Cell Environ 33:453–467

    Article  CAS  PubMed  Google Scholar 

  • Monti A, Brugnoli E, Scartazza A et al (2006) The effect of transient and continuous drought on yield, photosynthesis and carbon isotope discrimination in sugar beet (Beta vulgaris L.). J Exp Bot 57:1253–1262

    Article  CAS  PubMed  Google Scholar 

  • Pesacreta TC, Acharya A, Hasenstein KH (2021) Endogenous nutrients are concentrated in specific tissues in the Zea mays seedling. Protoplasma 258:863–878

    Article  CAS  PubMed  Google Scholar 

  • Posch S, Bennett LT (2009) Photosynthesis, photochemistry and antioxidative defence in response to two drought severities and with re-watering in Allocasuarina luehmannii. Plant Biol 11:83–93

    Article  CAS  PubMed  Google Scholar 

  • Puglielli G, Varone L, Gratani L et al (2017) Specific leaf area variations drive acclimation of Cistus salvifolius in different light environments. Photosynthetica 55:31–40

    Article  CAS  Google Scholar 

  • Reynolds JF, Kemp PR, Ogle K et al (2004) Modifying the “pulse-reserve” paradigm for deserts of North America: precipitation pulses, soil water, and plant responses. Oecologia 141:194–210

    Article  PubMed  Google Scholar 

  • Sánchez E, Scordia D, Lino G et al (2015) Salinity and water stress effects on biomass production in different Arundo donax L. clones. Bioenerg Res 8:1461–1479

    Article  Google Scholar 

  • Sánchez E, Gil S, Azcón-Bieto J et al (2016) The response of Arundo donax L. (C3) and Panicum virgatum (C4) to different stresses. Biomass Bioenerg 85:335–345

    Article  Google Scholar 

  • Siopongco JDLC, Yamauchi A, Salekdeh H et al (2006) Growth and water use response of doubled-haploid rice lines to drought and rewatering during the vegetative stage. Plant Prod Sci 9:141–151

    Article  Google Scholar 

  • Sofo A, Dichio B, Xiloyannis C et al (2014) Effects of different irradiance levels on some antioxidant enzymes and on malondialdehyde content during rewatering in Olea europaea. Plant Sci 166:293–302

    Article  Google Scholar 

  • Solanki JK, Sarangi SK (2014) Effect of drought stress on proline accumulation in peanut genotypes. Int J Adv Res 2:301–309

    Google Scholar 

  • Upadhyaha H, Panda SK, Dutta BK (2008) Variation of physiological and antioxidative responses in tee cultivars subjected to elevated water stress followed by rehydration recovery. Acta Physiol Plant 30:457–468

    Article  Google Scholar 

  • Valladares F, Gianoli E, Gómez JM (2007) Ecological limits to plant phenotypic plasticity. New Phytol 176:749–763

    Article  PubMed  Google Scholar 

  • van Kleunen M, Fischer M (2005) Constrains on the evolution of adaptive phenotypic plasticity in plants. New Phytol 166:49–60

    Article  PubMed  Google Scholar 

  • Violeta V, Tsonko T, Massimiliano T et al (2018) Physiological and structural adjustments of two ecotypes of Platanus orientalis L. from different habitats in response to drought and re-watering. Conserv Physiol 6:1–18

    Google Scholar 

  • Wang S, Callaway RM (2022) What does not kill you can make you stronger: variation in plasticity in response to early temporally heterogeneous hydrological experience. J Ecol 110:2418–2432

    Article  Google Scholar 

  • Wang X, Huang J (2015) Experimental principles and techniques of plant physiology and biochemistry. Higher Education, Beijing, pp 274–277

    Google Scholar 

  • Wang L, Li Q, Xu J et al (2015) Effects of drought stress to growth and morphological plasticity of different provenances of Artemisia ordosica seedlings. J Northeast Forestry Univ 43:55–78

    Google Scholar 

  • Wang S, Callaway RM, Zhou DW et al (2017) Experience of inundation or drought alters the responses of plants to subsequent water conditions. J Ecol 105:176–187

    Article  Google Scholar 

  • Wang Y, Ni F, Yin D et al (2021) Physiological response of Lagerstroemia indica (L.) Pers. seedlings to drought and rewatering. Trop Plant Biol 14:360–370

    Article  CAS  Google Scholar 

  • Wang D, Wang S, Li LX et al (2023) Contrasting effects of experiencing temporally heterogeneous light availability versus homogenous shading on plant subsequent responses to light conditions. BMC Plant Biol 23:232

    Article  PubMed  PubMed Central  Google Scholar 

  • Xu ZZ, Zhou GS (2005) Effects of water stress and nocturnal temperature on carbon allocation in the perennial grass, Leymus chinensis. Plant Physiol 123:272–280

    Article  CAS  Google Scholar 

  • Xu ZZ, Zhou GS (2007) Photosynthetic recovery of a perennial grass Leymus chinensis after different periods of soil drought. Plant Prod Sci 10:277–285

    Article  CAS  Google Scholar 

  • Xu ZZ, Zhou GS, Shimizu H (2009) Are plant growth and photosynthesis limited by pre-drought following rewatering in grass? J Exp Bot 60:3737–3749

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Xu Z, Zhou G, Shimizu H (2010) Plant responses to drought and rewatering. Plant Signal Behav 5:649–654

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Xu X, Wang H, Qi X et al (2014) Waterlogging-induced increase in fermentation and related gene expression in the root of cucumber (Cucumis sativus L.). Sci Hortic 179:388–395

    Article  CAS  Google Scholar 

  • Zhang MY, Yang ZQ, Hou MY (2017) Effects of soil water stress on photosynthetic characteristics and antioxidant enzyme system of cucumber leaves in greenhouse. Chin J Agrometeorol 38:21–30

    Google Scholar 

  • Zunzunegui M, Ain-Lhout F, Díaz Barradas MC et al (2009) Physiological, morphological and allocation plasticity of a semi-deciduous shrub. Acta Oecol 35:370–379

    Article  Google Scholar 

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Acknowledgements

The authors would like to thank Forest Resources and Environment Research Center in Guizhou Province for its support.

Funding

This work was supported by the Hunan Provincial Department of Education (Grant No. [2021]352-21A0473), Hunan Provincial Natural Science Foundation of China (Grant Nos. 2023JJ50258; 2023JJ50259).

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DW involved in conceptualization, methodology, software, data curation, original draft preparation, software, validation, and reviewing of the manuscript. Y-SW involved in conceptualization, visualization, supervision, and reviewing of the manuscript. Z-ZL and J-WX involved in conceptualization, visualization, methodology, investigation validation, and software.

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Correspondence to Deng Wang.

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Wang, D., Wang, YS., Li, ZZ. et al. Estimating the Morphological and Physiological Plasticity of Ligustrum obtusifolium Seedlings in Response to Drought Stress and Subsequent Rewatering. J Plant Growth Regul 43, 1592–1604 (2024). https://doi.org/10.1007/s00344-023-11208-4

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