Skip to main content
Log in

Drought priming at vegetative growth stages improves tolerance to drought and heat stresses occurring during grain filling in spring wheat

  • Original paper
  • Published:
Plant Growth Regulation Aims and scope Submit manuscript

Abstract

Plants of spring wheat (Triticum aestivum L. cv. Vinjett) were exposed to moderate water deficit at the vegetative growth stages six-leaf and/or stem elongation to investigate drought priming effects on tolerance to drought and heat stress events occurring during the grain filling stage. Compared with the non-primed plants, drought priming could alleviate photo-inhibition in flag leaves caused by drought and heat stress episodes during grain filling. In the primed plants, drought stress inhibited photosynthesis mainly through decrease of maximum photosynthetic electron transport rate, while decrease of the carboxylation efficiency limited photosynthesis under heat stress. The higher saturated net photosynthetic rate of flag leaves coincided with the lowered non-photochemical quenching rates in the twice-primed plants under drought stress and in the primed plants during stem elongation under heat stress. Compared to the non-priming treatment, drought priming either applied once or twice alleviated the grain yield reduction by drought stress during grain filling, and priming during the stem elongation stage alleviated yield loss by heat stress at grain filling. The higher concentration of abscisic acid in primed plants under drought stress could contribute to higher grain yield compared to the non-primed plants. Taken together, the results indicate that drought priming during vegetative stages improved tolerance to both drought and heat stress events occurring during grain filling in wheat.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1
Fig. 2
Fig. 3
Fig. 4

Similar content being viewed by others

Abbreviations

ABA:

Abscisic acid

Asat :

Saturated net photosynthetic rate

A/Ci curve:

Carbon assimilation versus intercellular CO2 concentration curve

Jmax :

Maximum photosynthetic electron transport rate

LRWC:

Leaf relative water content

PSII:

Photosystem II

NPQ:

Non-photochemical quenching of chlorophyll fluorescence

ΦPSII:

Actual PSII photochemical efficiency

Rubisco:

Ribulose-1,5-bisphosphate carboxylase/oxygenase

Vmax :

Maximum carboxylation rate of Rubisco

References

  • Ali M, Jensen C, Mogensen V, Andersen M, Henson I (1999) Root signalling and osmotic adjustment during intermittent soil drying sustain grain yield of field grown wheat. Field Crop Res 62:35–52

    Article  Google Scholar 

  • Asch F, Andersen MN, Jensen CR, Mogensen VO (2001) Ovary abscisic acid concentration does not induce kernel abortion in field-grown maize subjected to drought. Eur J Agron 15:119–129

    Article  CAS  Google Scholar 

  • Barnabas B, Jager K, Feher A (2008) The effect of drought and heat stress on reproductive processes in cereals. Plant Cell Environ 31:11–38

    CAS  Google Scholar 

  • Brestic M, Cornic G, Freyer MJ, Baker NR (1995) Does photorespiration protect the photosynthetic apparatus in French bean leaves from photoinhibition during drought stress? Planta 196:450–457

    Article  CAS  Google Scholar 

  • Bruce TJA, Matthes MC, Napier JA, Pickett JA (2007) Stressful “memories” of plants: evidence and possible mechanisms. Plant Sci 173:603–608

    Article  CAS  Google Scholar 

  • Chaves M, Davies B (2010) Drought effects and water use efficiency: improving crop production in dry environments. Funct Plant Biol 37:3–6

    Article  Google Scholar 

  • Conrath U (2011) Molecular aspects of defence priming. Trends Plant Sci 16:524–531

    Article  CAS  PubMed  Google Scholar 

  • Ding Y, Fromm M, Avramova Z (2012) Multiple exposures to drought ‘train’ transcriptional responses in Arabidopsis. Nat Commun 3:740

    Article  PubMed  Google Scholar 

  • Farooq M, Irfan M, Aziz T, Ahmad I, Cheema S (2013) Seed priming with ascorbic acid improves drought resistance of wheat. J Agron Crop Sci 199:12–22

    Article  CAS  Google Scholar 

  • Finkelstein RR, Gampala SSL, Rock CD (2002) Abscisic acid signaling in seeds and seedlings. Plant Cell 14:S15–S45

    PubMed Central  CAS  PubMed  Google Scholar 

  • Flexas J, Medrano H (2002) Drought-inhibition of photosynthesis in C3 plants: stomatal and non-stomatal limitations revisited. Ann Bot 89:183–189

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  • Flexas J, Bota J, Galmés J, Medrano H, Ribas-Carbó M (2006) Keeping a positive carbon balance under adverse conditions: responses of photosynthesis and respiration to water stress. Physiol Plant 127:343–352

    Article  CAS  Google Scholar 

  • Giardi M, Cona A, Geiken B, Kučera T, Masojidek J, Mattoo A (1996) Long-term drought stress induces structural and functional reorganization of photosystem II. Planta 199:118–125

    Article  CAS  Google Scholar 

  • Gusmao M, Siddique K, Flower K, Nesbitt H, Veneklaas E (2012) Water deficit during the reproductive period of grass pea (Lathyrus sativus L.) reduced grain yield but maintained seed size. J Agron Crop Sci 198:430–441

    Article  Google Scholar 

  • Ivanov A, Krol M, Maxwell D, Huner N (1995) Abscisic acid induced protection against photoinhibition of PSII correlates with enhanced activity of the xanthophyll cycle. FEBS Lett 371:61–64

    Article  CAS  PubMed  Google Scholar 

  • Jiang MY, Zhang JH (2004) Abscisic acid and antioxidant defense in plant cells. Acta Bot Sin 46:1–9

    CAS  Google Scholar 

  • Krasensky J, Jonak C (2012) Drought, salt, and temperature stress-induced metabolic rearrangements and regulatory networks. J Exp Bot 63:1593–1608

    Article  CAS  PubMed  Google Scholar 

  • Larkindale J, Knight MR (2002) Protection against heat stress-induced oxidative damage in Arabidopsis involves calcium, abscisic acid, ethylene, and salicylic acid. Plant Physiol 128:682–695

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  • Lawlor DW (2002) Limitation to photosynthesis in water-stressed leaves: stomata vs. metabolism and the role of ATP. Ann Bot 89:871–885

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  • Lawlor DW, Tezara W (2009) Causes of decreased photosynthetic rate and metabolic capacity in water-deficient leaf cells: a critical evaluation of mechanisms and integration of processes. Ann Bot 103:561–579

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  • Li C, Jiang D, Wollenweber B, Li Y, Dai T, Cao W (2011) Waterlogging pretreatment during vegetative growth improves tolerance to waterlogging after anthesis in wheat. Plant Sci 5:672–678

    Article  Google Scholar 

  • Liu F, Andersen MN, Jensen CR (2003) Loss of pod set caused by drought stress is associated with water status and ABA content of reproductive structures in soybean. Funct Plant Biol 30:271–280

    Article  CAS  Google Scholar 

  • Liu F, Jensen CR, Andersen MN (2005) A review of drought adaptation in crop plants: changes in vegetative and reproductive physiology induced by ABA-based chemical signals. Aust J Agric Res 56:1245–1252

    Article  CAS  Google Scholar 

  • Lu C, Zhang J (1999) Effects of water stress on photosystem II photochemistry and its thermostability in wheat plants. J Exp Bot 50:1199–1206

    Article  CAS  Google Scholar 

  • Ma Q-Q, Wang W, Li Y-H, Li D-Q, Zou Q (2006) Alleviation of photoinhibition in drought-stressed wheat (Triticum aestivum) by foliar-applied glycinebetaine. J Plant Physiol 163:165–175

    Article  CAS  PubMed  Google Scholar 

  • Pastor V, Luna E, Mauch-Mani B, Ton J, Flors V (2012) Primed plants do not forget. Environ Exp Bot 94:46–56

    Article  Google Scholar 

  • Porter JR, Gawith M (1999) Temperatures and the growth and development of wheat: a review. Eur J Agron 10:23–36

    Article  Google Scholar 

  • Possell M, Ryan A, Vickers CE, Mullineaux PM, Hewitt CN (2010) Effects of fosmidomycin on plant photosynthesis as measured by gas exchange and chlorophyll fluorescence. Photosynth Res 104:49–59

    Article  CAS  PubMed  Google Scholar 

  • Reddy AR, Chaitanya KV, Vivekanandan M (2004) Drought-induced responses of photosynthesis and antioxidant metabolism in higher plants. J Plant Physiol 161:1189–1202

    Article  CAS  Google Scholar 

  • Reynolds M, Balota M, Delgado M, Amani I, Fischer R (1994) Physiological and morphological traits associated with spring wheat yield under hot, irrigated conditions. Func Plant Biol 21:717–730

    Google Scholar 

  • Sharkey TD, Bernacchi CJ, Farquhar GD, Singsaas EL (2007) Fitting photosynthetic carbon dioxide response curves for C3 leaves. Plant Cell Environ 30:1035–1040

    Article  CAS  PubMed  Google Scholar 

  • Souza R, Machado E, Silva J, Lagôa A, Silveira J (2004) Photosynthetic gas exchange, chlorophyll fluorescence and some associated metabolic changes in cowpea (Vigna unguiculata) during water stress and recovery. Environ Exp Bot 51:45–56

  • Walter J, Jentsch A, Beierkuhnlein C, Kreyling J (2012) Ecological stress memory and cross stress tolerance in plants in the face of climate extremes. Environ Exp Bot 94:3–8

    Article  Google Scholar 

  • Wang X, Cai J, Jiang D, Liu F, Dai T, Cao W (2011) Pre-anthesis high-temperature acclimation alleviates damage to the flag leaf caused by post-anthesis heat stress in wheat. J Plant Physiol 6:585–593

    Article  Google Scholar 

  • Weldearegay DF, Yan F, Jiang D, Liu F (2012) Independent and combined effects of soil warming and drought stress during anthesis on seed set and grain yield in two spring wheat varieties. J Agron Crop Sci 198:245–253

    Article  Google Scholar 

  • Yang J, Zhang J (2006) Grain filling of cereals under soil drying. New Phytol 169:223–236

    Article  CAS  PubMed  Google Scholar 

  • Yang J, Zhang J, Wang Z, Zhu Q, Wang W (2001) Hormonal changes in the grains of rice subjected to water stress during grain filling. Plant Physiol 127:315–323

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  • Zhang X, Wollenweber B, Jiang D, Liu F, Zhao J (2008) Water deficits and heat shock effects on photosynthesis of a transgenic Arabidopsis thaliana constitutively expressing ABP9, a bZIP transcription factor. J Exp Bot 59:839–848

    Article  CAS  PubMed  Google Scholar 

Download references

Acknowledgments

We are grateful for financial support from the Chinese Scholarship Council for the stay of X.W. in Denmark and from the Danish Ministry for Agriculture (to B.W.) for this study. We are grateful for the skillful help of the technicians at the Research Centre Flakkebjerg of Aarhus University.

Author information

Authors and Affiliations

Authors

Corresponding authors

Correspondence to Dong Jiang or Bernd Wollenweber.

Rights and permissions

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Wang, X., Vignjevic, M., Liu, F. et al. Drought priming at vegetative growth stages improves tolerance to drought and heat stresses occurring during grain filling in spring wheat. Plant Growth Regul 75, 677–687 (2015). https://doi.org/10.1007/s10725-014-9969-x

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s10725-014-9969-x

Keywords

Navigation