Effect of Imbibition Time on Hormonal Changes of Germinating Tamarindus indica and Prosopis juliflora

Authors

  • B. A. Kyari Department of Biological Sciences University of Maiduguri, Borno State, Nigeria
  • Z. A. Lawan Remedial Science Ramat Polytechnic, Maiduguri, Borno State, Nigeria
  • M. S. Waziri Department of Biological Sciences University of Maiduguri, Borno State, Nigeria
  • H. M. Ajiri Chad Basing Development Programme, Maiduguri, Borno State, Nigeria
  • B. Apagu Department of Biological Sciences University of Maiduguri, Borno State, Nigeria
  • H. Mari Department of Biological Sciences University of Maiduguri, Borno State, Nigeria
  • M. A. Ibrahim Department of Biological Sciences, University of Maiduguri

DOI:

https://doi.org/10.32734/injar.v5i03.6573

Keywords:

germination, imbibition, plant hormone, Prosopis juliflora, Tamarindus indica

Abstract

Imbibition time and hormonal changes play a significant role in seed germination. This study, evaluated the effects of some phytohormones; indole acetic acid (IAA), abscisic acid (ABA), gibberellin and cytokinins) and imbibition time (0, 48 and 96 hours) on Tamarindus indica and Prosopis juliflora. High-Performance Liquid Chromatography (HPLC) was used to determine the concentrations of the hormones. Results indicated significantly higher and faster in P. juliflora than T. indica. The germination rate was 4.1 - 68.1% and 4.0 - 61.4%, and model for inhibition time 28.256ln(x) and 25.791ln(x), respectively. Similarly, results also expressed highly significant variable changes in the concentrations of the four studied phytohormones between T. indica (0.491 - 0.705 mg/ml) and P. Juliflora (0.109 - 1.130 mg/ml). The concentrations of IAA and ABA were significantly higher by 60.6% and 77.7% in the seeds of T. indica than P. juliflora, respectively. P. juliflora had 37.6% and 12.5% higher cytokinin and gibberellin than T. indica, respectively. Cytokinin (0.7951 - 1.0939 mg/ml), gibberellins (0.535 - 0.757 mg/ml), IAA (0.363 - 0.419 mg/ml) and ABA (0.250 - 0.335 mg/ml) also varied significantly over the periods. In general, cytokinin and gibberellins increased by 8.1 - 27.3% and 22.9 - 23.0%, while that of IAA and ABA decreased 13.6 - 15.4% and 26.4 - 34.0%, over the imbibitions time of 0-96 hours. In conclusion, higher germination of P. juliflora is attributed to cytokinin and gibberellins, and the lower germination in T. indica to the higher inhibitory effects of IAA and ABA.

Downloads

Download data is not yet available.

References

K. S. et al., “Forest restoration research in northern Thailand. 1. Fruits, seeds and seedlings of Hovenia dulcis Thunb,” Nat. Hist. Bull. SSiam. Soc, vol. 44, pp. 41–52, 1996.

V. L. Engel and J. A. Parrotta “An evaluation of direct seeding for reforestation of degraded lands in central Sao Paulo state, Brazil,” Forest Ecology and Management, vol. 152, pp. 169–181, 2001.

K. G. Gangopadhyay, V. K. Dobhal, K. C. Bhatt, and B. S. Dhillon, “Status of horticultural crop genetic resources in India,” Indian Journal of Plant Genetic Resources, vol. 17, no. 2, pp. 89-104, 2004.

M. A. Elfadle and O. Luukkanen, “Field studies on ecological strategies of Prosopis juliflora in a dry land ecosystem,” Journal of Arid Environment, vol. 66, no. 1, pp. 1–15, 2006.

K. Hermann et al., “1-Aminocyclopropane-1-carboxylic acid and abscisic acid during the germination of sugar beet (Beta vulgaris L. ) - A comparative study of fruits and seeds,” J. Exp. Bot, vol. 58, pp. 3047–3060, 2007.

T. E. Olagunju, “Drought, desertification and the Nigerian environment: A review,” Journal of Ecology and the Natural Environment, vol. 7, no. 7, pp. 196–209, 2015.

B. Dehgan, “Effect of seed scarification and gibberellic acid treatment on seedling emergence of sky-blue lupine (Lupinus diffuses),” Journal of Environmental Horticulture, vol. 21, no. 2, pp. 64–67, 2003.

J. M. Baskin and C. C. Baskin, “A classification system for seed dormancy,” Seed Sci. Res., vol. 14, no. 1, pp. 1–16, 2004.

R. L. Benech-Arnold, N. Gualano, J. Leymarie, D. Côme, and F. Corbineau, “Hypoxia interferes with ABA metabolism and increases ABA sensitivity in embryos of dormant barley grains,” J. Exp. Bot., vol. 57, no. 6, pp. 1423–1430, 2006.

W. E. Finch-Savage and G. Leubner-Metzger, “Seed dormancy and the control of germination: Tansley review,” New Phytol., vol. 171, no. 3, pp. 501–523, 2006.

D. Soyler, K.M. Khawar “Effects of prechilling, scarification, incubation, temperature, photoperiod, KNO3 and GA3 treatments on germination of Caper (Capparis ovate Desf),” Var. Palaestina Zoh. seeds. Propagation of Ornamental Plants, vol. 6, pp. 159–164, 2006.

M. K. Suleiman, N. R. Bhat, M. S. Abdal, and S Jacob, “Effect of acid scarification and warm water treatments on germination of dry seeds of Capparis sponsa,” African Journal of Biotechnology, vol. 5, no. 3, pp. 199–203, 2008.

F. P. O. Mollard and P. Insausti, “Breaking Setaria parviflora seed dormancy by nitrates and light is part of a mechanism that detects a drawdown period after flooding,” Aquat. Bot., vol. 91, no. 1, pp. 57–60, 2009.

K. Muller, S. Tintelnot, and G. Leubner-Metzger, “Endosperm limited Brassicaceae seed germination: abscisic acid inhibits embryo-induced endosperm weakening of Lepidium sativum (cress) and endosperm rupture of cress and Arabidopsis thaliana,” Plant Cell Physiol, vol. 47, pp. 864–877, 2006.

Y. Xu et al., “Effects of SAG12-ipt expression on cytokinin production, growth and senescence of creeping bentgrass (Agrostis stolonifera L.) under heat stress”. Plant Growth Regulation, vol. 57, pp. 281-291, 2009.

K. Graeber, K. Nakabayashi, E. Miatton, G. Leubner-Metzger, and W. J. J. Soppe, “Molecular mechanisms of seed dormancy: Molecular mechanisms of seed dormancy,” Plant Cell Environ., vol. 35, no. 10, pp. 1769–1786, 2012.

M. Koornneef et al.,“Seed dormancy and germination. Curr. Opin. Plant Biol., 5: 33-36, 2002.

R. Hooley, “Gibberellins: perception, transduction and responses,” Plant Mol. Biol., vol. 26, no. 5, pp. 1529–1555, 1994.

S.-Y. Chen, S.-R. Kuo, and C.-T. Chien, “Roles of gibberellins and abscisic acid in dormancy and germination of red bayberry (Myrica rubra) seeds,” Tree Physiol., vol. 28, no. 9, pp. 1431–1439, 2008.

K. Graeber, A. Linkies, K. Müller, A. Wunchova, A. Rott, and G. Leubner-Metzger, “Cross-species approaches to seed dormancy and germination: conservation and biodiversity of ABA-regulated mechanisms and the Brassicaceae DOG1 genes,” Plant Mol. Biol., vol. 73, no. 1–2, pp. 67–87, 2010.

M. J., T. D. Y., B. C. C., and B. J. M, “Role of trichomes and pericarp in the seed biology of desert annual Lachnoloma lehmannii (Brassicaceae),” Ecol Res, vol. 29, pp. 33–44, 2014.

A. Atia et al., “ABA, GA3, and nitrate may control seed germination of Crithmum maritimum (Apiaceae) under saline conditions”. Comptes Rendus Biologies, 332(8), 704-710. doi:10.1016/j.crvi.2009.03.009.

J. D. Bewley, “Breaking down the walls: a role for endo-β-mannanase in release from seed dormancy,” Trends Plant Sci, vol. 2, pp. 464–469, 1997.

M. Miransari, D. Smith “Rhizobial lipo-chitooligosaccharides and gibberellins enhance barley (Hordum vulgare L) seed germination”. Biotechnol, vol. 8, pp. 270–275, 2009.

M. Miransari, D. Smith “Plant hormones and seed germination,” Environmental and Experimental Botany, vol. 99, pp. 110–121, 2014.

N. V. Obroucheva and O. V. Antipova, “Physiology of the initiation of seed germination,” Russ. J. Plant Physiol, vol. 44, pp. 250–264, 1997.

P. Schopfer and C. Plachy, “Control of seed germination by abscisic acid: effect on embryo water uptake in Brassica napus L,” Plant Physiol, vol. 76, pp. 155–160, 1984.

G. Leubner-Metzger, “Brassinosteroids and gibberellins promote tobacco seed germination by distinct pathways,” Planta, vol. 213, no. 5, pp. 758–763, 2001

M. Miransari, D.L. Smith, “The role of hormones during seed development and germination,” Kluwer Academic, 2004.

L. Lopez-Molina, S. Mongrand, and N. H. Chua, “A post germination developmental arrest checkpoint is mediated by abscisic acid and requires ABI5 transcription factor in Arabidopsis,” Proc. Natl. Acad. Sci. USA, vol. 98, pp. 4782–4787, 2001.

S. N. and S. P, “Influence of water floatation technique on seed and seedling quality characteristics of Sesamum indicum,” Journal of Agriculture and Veterinary Science, vol. 7, no. 8, pp. 51–53, 2014.

T. Y., W. L., M. C., L. J., L. B., and L. H, “The use of HPLC in determination of endogenous hormones in anthers of bitter melon,” Journal of Life Sciences, vol. 5, pp. 139–142, 2010.

P. Achard, J.-P. Renou, R. Berthomé, N. P. Harberd, and P. Genschik, “Plant DELLAs Restrain Growth and Promote Survival of Adversity by Reducing the Levels of Reactive Oxygen Species,” Current Biology, vol. 18, no. 9, pp. 656–660, 2008.

S. Ali-Rachedi et al., "Changes in endogenous abscisic acid levels during dormancy release and maintenance of mature seeds: studies with the Cape Verde Islands ecotype, the dormant model of Arabidopsis thaliana," Planta, vol. 219, no. 3, 2004. Available: 10.1007/s00425-004-1251-4.

A. J. Matilla and M. A. Matilla-Vázquez, “Involvement of ethylene in seed physiology,” Plant Sci., vol. 175, no. 1–2, pp. 87–97, 2008.

R. D. Castro and H. W. M. Hilhorst, “Plant hormonal control of seed development in GA and ABA-deficient tomato (Lycopersicon esculentum Mill. cv Money-maker) mutants,” Plant Sci, vol. 170, pp. 462–470, 2006.

Q. Ali, M. Ahsan, M. Tahir, M. Waseem, J. Farooq, M. Elahi, and M. Sadique, “Genetic variability for grain yield and quality traits in chickpea (Cicer arietinum L.),” International Journal for Agro Veterinary and Medical Sciences, vol. 5, no. 2, p. 201, 2011.

Published

2023-06-16

How to Cite

Kyari, B. A., Lawan, Z. A., Waziri, M. S. ., Ajiri, H. M., Apagu, B., Mari, H. ., & Ibrahim, M. A. (2023). Effect of Imbibition Time on Hormonal Changes of Germinating Tamarindus indica and Prosopis juliflora. Indonesian Journal of Agricultural Research, 5(3), 219 - 230. https://doi.org/10.32734/injar.v5i03.6573