Skip to main content
Log in

Seed priming with gibberellic acid rescues chickpea (Cicer arietinum L.) from chilling stress

  • Original Article
  • Published:
Acta Physiologiae Plantarum Aims and scope Submit manuscript

Abstract

Chickpea is sensitive to low temperature stress, especially during germination and stand establishment. Present study was planned to rescue the chickpea seedlings from chilling stress through seed priming with gibberellic acid. A study comprising of two chickpea cultivars (cv.) viz. Çağatay (a chilling tolerant cultivar: CTC) and Akçin (a chilling sensitive cultivar: CSC) in combination with 0, hydropriming, 5 µM, 10 µM, 15 µM, 20 µM gibberellic acid (GA3) seed priming treatments was tested in completely randomized design under chilling temperature. Primed and unprimed seeds were sown at 9 ± 0.5 °C day temperature for 14 h and 7 ± 0.5 °C night temperatures for 10 h. Final emergence percentage (FEP) in both cultivars was noted higher in 10 µM GA3 seed priming. Coefficient of uniformity of emergence (CUE) was increased and time taken to 50% emergence (E50) was shorten with the application of 5 or 15 µM GA3. Mean emergence time (MET) was reduced in both cultivars in 20 µM GA3 seed treatment. Emergence energy (EE) and emergence index (EI) of CTC were increased in 15 µM GA3. In CSC 5 µM GA3, seed treatment was most productive treatment under low temperature. Higher doses of GA3 seed treatments in CSC were proved very effective in maintaining high relative water contents and low electrolyte leakage. Plant height, root length and number of flowers were also increased in GA3 primed treatments. In conclusion, seed priming with GA3 can be used in chickpea for good stand establishment, crop growth, reducing electrolyte leakage and maintaining high relative water contents.

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
Fig. 5
Fig. 6
Fig. 7
Fig. 8
Fig. 9

Similar content being viewed by others

References

  • Ali HM, Siddiqui MH, Basalah MO, Al-Whaibi MH, Sakran AM, Al-Amri A (2012) Effects of gibberellic acid on growth and photosynthetic pigments of Hibiscus sabdariffa L. under salt stress. Afr J Biotechnol 11:800–804

    CAS  Google Scholar 

  • AOSA (1990) Rules for testing seeds, USA. J Seed Technol 12:1–112

    Google Scholar 

  • Baalbaki RZ, Zurayk RA, Blelk MM, Tahouk SN (1999) Germination and seedling development of drought tolerant and susceptible wheat under moisture stress. Seed Sci Technol 27:291–302

    Google Scholar 

  • Barrs H, Weatherley P (1962) A re-examination of the relative turgidity technique for estimating water deficits in leaves. Aust J Biol Sci 15:413–428

    Google Scholar 

  • Bewley J, Black M (1994) Seeds: physiology of development and germination. Plenum Press, New York, USA, p 445

    Google Scholar 

  • Blum A, Ebercon A (1981) Cell membrane stability as a measure of drought and heat tolerance in wheat. Crop Sci 21:43–47

    Google Scholar 

  • Cardoso JC, Ono EO, Rodrigues JD (2012) Gibberellic Acid (GA3) on flowering induction and quality of Phalaenopsis orchid. Ornamental Hort 18:135–140

    Google Scholar 

  • Chavan N, Bhujbal G, Manjare M (2014) Effect of seed priming on field performance and seed yield of soybean [Glycine max (L.) Merill] varieties. Bioscan 9:111–114

    Google Scholar 

  • Chen D, Gunawardena T, Naidu B, Fukai S, Basnayake J (2005) Seed treatment with gibberellic acid and glycinebetaine improves seedling emergence and seedling vigour of rice under low temperature. Seed Sci Technol 33:471–479

    Google Scholar 

  • Coolbear P, Francis A, Grierson D (1984) The effect of low temperature pre-sowing treatment on the germination performance and membrane integrity of artificially aged tomato seeds. J Exp Bot 35:1609–1617

    CAS  Google Scholar 

  • Croser J, Clarke H, Siddique K, Khan T (2003) Low-temperature stress: implications for chickpea (Cicer arietinum L.) improvement. Crit Rev Plant Sci 22:185–219

    Google Scholar 

  • Dong B, Deng Y, Wang H, Gao R, Stephen GUK, Chen S, Jiang J, Chen F (2017) Gibberellic acid signaling is required to induce flowering of chrysanthemums grown under both short and long days. Int J Mol Sci 18:1259

    PubMed Central  Google Scholar 

  • Ellis R, Roberts E (1981) The quantification of ageing and survival in orthodox seeds. Seed Sci Technol 9:373–409

    Google Scholar 

  • Farooq M, Hussain M, Nawaz A, Lee DJ, Alghamdi SS, Siddique KH (2017) Seed priming improves chilling tolerance in chickpea by modulating germination metabolism, trehalose accumulation and carbon assimilation. Plant Physiol Biochem 111:274–283

    CAS  PubMed  Google Scholar 

  • Farooq M, Basra SMA, Hafeez K (2006) Seed invigoration by osmohardening in coarse and fine rice. Seed Sci Technol 34:181–187

    Google Scholar 

  • Farooq M, Basra SMA, Ahmad N, Hafeez K (2005) Thermal hardening: a new seed vigor enhancement tool in rice. J Integr Plant Biol 47:187–193

    Google Scholar 

  • Farooq M, Aziz T, Basra SMA, Wahid A, Khaliq A, Cheema MA (2008) Exploring the role of calcium to improve chilling tolerance in hybrid maize. J Agron Crop Sci 194:350–359

    Google Scholar 

  • Flower D, Ludlow M (1986) Contribution of osmotic adjustment to the dehydration tolerance of water-stressed pigeon pea (Cajanus cajan (L.) millsp.) leaves. Plant Cell Environ 9:33–40

    Google Scholar 

  • Georgia G, Ilias I, Anastasia I, Parthena G (2010) Comparative study on the effects of various plant growth regulators on growth, quality and physiology of Capsicum annuum L. Pak J Bot 42:805–814

    Google Scholar 

  • Ghodrat V, Rousta MJ (2012) Effect of priming with gibberellic acid (GA3) on germination and growth of corn (Zea mays L.) under saline conditions. Int J Agri Crop Sci 4:883–885

    Google Scholar 

  • Ghosh T, Rai M, Tyagi W, Challam C (2016) Seedling stage low temperature response in tolerant and susceptible rice genotypes suggests role of relative water content and members of OsSNAC gene family. Plant Signal Behav 11:e1138192

    PubMed  PubMed Central  Google Scholar 

  • Gupta R, Chakrabarty S (2013) Gibberellic acid in plant: still a mystery unresolved. Plant Signal Behav 8:25504

    Google Scholar 

  • Harris D, Joshi A, Khan P, Gothkar P, Sodhi P (1999) On-farm seed priming in semi-arid agriculture: development and evaluation in maize, rice and chickpea in India using participatory methods. Exp Agric 35:15–29

    Google Scholar 

  • Hartmann HT, Kester DE, Davies FT, Geneve RL (1997) Plant Propagation, Principles and Practices, 6th edn. Prentice Hall, Upper Saddle River, N.J., USA, p 770

    Google Scholar 

  • Jasmine MS, John MA (2012) Effects of gibberellic acid on seedling growth, chlorophyll content and carbohydrate metabolism in okra (Abelmoschus esculentus L. Moench) genotypes under saline stress. Res J Chem Sci 2(7):72–74

    Google Scholar 

  • Jukanti AK, Gaur PM, Gowda C, Chibbar RN (2012) Nutritional quality and health benefits of chickpea (Cicer arietinum L.): a review. Br J Nutr T 108:11–26

    Google Scholar 

  • Kaur S, Gupta AK, Kaur N (1998) Gibberellic acid and kinetin partially reverse the effect of water stress on germination and seedling growth in chickpea. Plant Growth Reg 25:29–33

    CAS  Google Scholar 

  • Kaya C, Tuna AL, Alfredo AA (2006) Gibberellic acid improves water deficit tolerance in maize plants. Acta Physiol Plant 28:331–337

    CAS  Google Scholar 

  • Khan MR, Qureshi AS, Hussain SA, Ibrahim M (2005) Genetic variability induced by gamma irradiation and its modulation with gibberellic acid in M~ 2 generation of chickpea (Cicer arietinum L.). Pak J Bot 37:285

    Google Scholar 

  • Kirmizi S, Güleryüz G, Arslan H, Sakar HS (2010) Effects of moist chilling, gibberellic acid, and scarification on seed dormancy in the rare endemic Pedicularis olympica (Scrophulariaceae). Turk J Bot 34:225–232

    Google Scholar 

  • Koch K (1996) Carbohydrate-modulated gene expression in plants. Ann Rev Plant Bio 47:509–540

    CAS  Google Scholar 

  • Kuiper P (1985) Environmental changes and lipid metabolism of higher plants. Physiol Plant 64:118–122

    CAS  Google Scholar 

  • Kulkarni M, Chimmad V (2014) Effect of temperature regimes on phenology and yield of chickpea (Cicer arietinum L.). Karnataka J Agric Sci 27:526–527

    Google Scholar 

  • Lafitte (2002) Relationship between leaf relative water content during reproductive stage water deficit and grain formation in rice. Field Crops Res 76:165–174

    Google Scholar 

  • Lee SS, Kim JH (2000) Total sugars, α-amylase activity, and germination after priming of normal and aged rice seeds. Kor J Crop Sci 45:108–111

    Google Scholar 

  • Leshem YL, Cojocaru M, MargelEL-ANI SD, Landau EM (1990) A biophysical study of abscisic acid interaction with membrane phospholipid components. New Phytol 116:487–498

    CAS  Google Scholar 

  • Lim SC, Kim SK, Kim YH, Youn CK, Yoon T (2004) Vine growth and fruit quality of ‘kyoho’ grapes as affected by Mepiquat chloride and GA3. Acta Hort (ISHS) 653:145–149

    CAS  Google Scholar 

  • Little C, MacDonald JE (2003) Effects of exogenous gibberellin and auxin on shoot elongation and vegetative bud development in seedlings of Pinus sylvestris and Picea glauca. Tree Physiol 23:73–83

    CAS  PubMed  Google Scholar 

  • Lyons J (2012) Low temperature stress in crop plants: the role of the membrane. Elsevier 4(6):413–444

    Google Scholar 

  • Mazliak P (1983) Plant Membrane Lipids: Changes and Alterations during Aging and Senescence. In: Lieberman M (ed) Post-harvest physiology and crop preservation. Nato advanced study institutes series (series a: life sciences), vol 46. Springer, Boston, MA, pp 123–140

    Google Scholar 

  • Moon BY, Higashi S, Gombos Z, Murata N (1995) Unsaturation of the membrane lipids of chloroplasts stabilizes the photosynthetic machinery against low-temperature photoinhibition in transgenic tobacco plants. Proce Ntl Acad Sci 92:6219–6223

    CAS  Google Scholar 

  • Morris DA, Arthur ED (1985) Effects of gibberellic acid on patterns of carbohydrate distribution and acid invertase activity in Phaseolus vulgaris. Physiol Plant 65:257–262

    CAS  Google Scholar 

  • Naylor AW (1984) Hormonal regulation of development. II. The function of hormones from the level of the cell to whole plant. In: Encyclopedia of Plant Physiology, Scott TK (ed) New Se ries. 10: 180–185. Berlin: Springer Verlag

  • Pham Thi A, Flood C, da Silva JA (1982) Effects of water stress on lipids and fatty acid composition of cotton leaves. Deve Plant Biol 62:219–224

    Google Scholar 

  • Pipinis E, Milios E, Kiamos N, Mavrokordopoulou O, Smiris P (2012) Effects of stratification and pre-treatment with gibberellic acid on seed germination of two Carpinus species. Seed Sci Technol 40:21–31

    Google Scholar 

  • Quartacci MF, Pinzino C, Sgherri CL, Navari-Izzo F (1995) Lipid composition and protein dynamics in thylakoids of two wheat cultivars differently sensitive to drought. Plant Physiol 108:191–197

    CAS  PubMed  PubMed Central  Google Scholar 

  • Ramteke V, Paithankar D, Baghel MM, Kurrey VK (2016) Impact of GA3 and propagation media on growth rate and leaf chlorophyll content of papaya seedlings. Res J Agri Sci 7:169–171

    Google Scholar 

  • Rehman S, Park IH (2000) Effect of scarification, GA and chilling on the germination of goldenrain-tree (Koelreuteria paniculata Laxm.) seeds. Sci Hortic 85:319–324

    CAS  Google Scholar 

  • Sabater B, Rodriquez MT (1978) Control of chlorophyll degradation in detached leaves of barley and oat through effect of kinetin on chlorophyllase levels. Physiol Plant 43:274–276

    CAS  Google Scholar 

  • Sacher J, Hatch M, Glasziou K (1963) Sugar accumulation cycle in sugar cane. III. Physical and metabolic aspects of cycle in immature storage tissues. Plant Physiol 38:348

    CAS  PubMed  PubMed Central  Google Scholar 

  • Shahzad R, Khan J, Gurmani AR, Waqas M, Hamayun M, Khan AL, Kang SM, Lee IJ (2014) Seed priming with gibberellic acid (GA3) in sponge-gourd modulated high salinity stress. J Life Sci 02:75–86

    Google Scholar 

  • Singh I, Kumar U, Singh S, Gupta C, Singh M, Kushwaha S (2012) Physiological and biochemical effect of 24-epibrassinoslide on cold tolerance in maize seedlings. Physiol Mol Biol Plants 18:229–236

    CAS  PubMed  PubMed Central  Google Scholar 

  • Singh K, Malhotra R, Saxena M (1993) Relationship between cold severity and yield loss in chickpea (Cicer arietinum L.). J Agron Crop Sci 170:121–127

    Google Scholar 

  • Szopińska D, Politycka B (2016) The effects of hydro-and osmopriming on the germination, vigour and hydrolytic enzymes activity of common zinnia (Zinnia elegans Jacq.) seeds. Folia Horticulturae 28:3–11

    Google Scholar 

  • Taiz L, Zeiger E (2006) Plant physiology, 4th edn. Sinauer Associates Inc., Publishers, Massachusetts

    Google Scholar 

  • Tatar O, Ozalkan C, Atasoy GD (2013) Partitioning of dry matter, proline accumulation, chlorophyll content and antioxidant activity of chickpea (Cicer arietinum L.) plants under chilling stress. Bul J Agri Sci 19(2):260–265

    Google Scholar 

  • Thakare U, Patil N, Malpathak N (2011) Performance of chick pea under the influence of gibberellic acid and oxygenated peptone during germination. Adv Biosci Biotech 2(01):40–45

    CAS  Google Scholar 

  • Trewavas A, Gilroy S (1991) Signal transduction in plant cells. Trends Genet 7:356–361

    CAS  PubMed  Google Scholar 

  • Van Volkenburgh E, Boyer JS (1985) Inhibitory effects of water deficit on maize leaf elongation. Plant Physiol 77:190–194

    PubMed  PubMed Central  Google Scholar 

  • Watkinson JI, Pill WG (1998) Gibberellic acid and presowing chilling increase seed germination of Indiangrass [Sorghastrum nutans (L.) Nash.]. HortScience 33:849–851

    CAS  Google Scholar 

  • Williams W (1990) Cold-induced lipid phase transitions. Phil Trans R Soc Lond B 326:555–570

    CAS  Google Scholar 

  • Wu LL, Mitchell JP, Cohn NS, Kaufman PB (1993) Gibberellin (GA3) enhances cell wall invertase activity and mRNA levels in elongating dwarf pea (Pisum sativum) shoots. Int J Plant Sci 154:280–289

    CAS  PubMed  Google Scholar 

  • Yadav S (2010) Cold stress tolerance mechanisms in plants. A Rev Agron Sustain Dev 30:515–527

    CAS  Google Scholar 

  • Yusefi-Tanha E, FallahTadayon SA (2015) Effect of seed priming on some effective physiological parame- ters on seed germination of pea (Pisum sativum L.) under chilling stress. J Plant Process and Function 4:1–15

    Google Scholar 

  • Yusefi TE, Fallah S, Taddayon A (2015) Effect of seed priming on some effective physiological parameters on seed germination of pea (Pisum sativum L.) under chilling stress. J Plant Pro Fun 13:1–15

    Google Scholar 

  • Yasseen BT (1983) An analysis of the effects of salinity on leaf growth in Mexican wheats. Thesis, The University of Leeds, UK

  • Zhou Y, Lam HM, Zhang J (2007) Inhibition of photosynthesis and energy dissipation induced by water and high light stresses in rice. J Exp Bot 58:1207–1217

    CAS  PubMed  Google Scholar 

  • Zhang N, Xie YD, Guo HJ, Zhao LS, Xiong HC, Gu JY, Li JH, Kong FQ, Sui L, Zhao ZW, Zhao SR, Liu LX (2016) Gibberellins regulate the stem elongation rate without affecting the mature plant height of a quick development mutant of winter wheat (Triticum aestivum L.). Plant Physiol Biochem 107:228–236

    CAS  PubMed  Google Scholar 

Download references

Acknowledgements

The author is thankful to The Scientific and Technological Research Council of Turkey (TÜBİTAK) for awarding scholarship grant under the BIDEB 2215 program for international students. The authors are also thankful to Ondokuz Mayıs University for providing funding for research project under the program of Scientific and Research Support Funds (PYO.ZRT.1901.15.009).

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Tariq Aziz.

Additional information

Communicated by J. Gao.

Publisher's Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Rights and permissions

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Aziz, T., Pekşen, E. Seed priming with gibberellic acid rescues chickpea (Cicer arietinum L.) from chilling stress. Acta Physiol Plant 42, 139 (2020). https://doi.org/10.1007/s11738-020-03124-x

Download citation

  • Received:

  • Revised:

  • Accepted:

  • Published:

  • DOI: https://doi.org/10.1007/s11738-020-03124-x

Keywords

Navigation