Madras Agric. J., 97 (1-3): 31-32, March 2010

Short Note

Optimization of Dormancy Breaking Treatments for Germination Improvement of Glory Lily (Gloriosa superba L.) Seeds B. Venudevan*, S. Sundareswaran and A. Vijayakumar Department of Seed Science and Technology, Seed Centre Tamil Nadu Agricultural University, Coimbatore-641 003

An experiment conducted to optimize the seed dormancy breaking treatment in Glory lily (Gloriosa superba L.) revealed that soaking the seeds in hot water (boiled to 100° C and removed from the flame) for 40 minutes had effectively improved the seed germination (62 %), seedling length (27.1 cm), seedling dry matter (181.0 mg) and vigour index (1680) accompanied with less hard seeds (15 %) and minimum abnormal seedlings (14 %), compared to acid scarification with concentrated H2SO4 for 2 minutes that improved the germination (52 %) over non-scarified seeds (22 %), but led to the development of abnormal seedlings (14 %) and dead seeds (12 %) at an increased level. Key words: Glory lily, seed dormancy, hot water soaking, germination, vigor

Gloriosa superba L. belonging to the family Liliaceae commonly known as glory lily, superb lily, tiger lily or tiger claws, is an important medicinal plant of the Tropics (Ridley, 1924). The glory lily is native to both Asia and Africa. Paramasivam and Arumugam, (1991) reported that major problems in the cultivation of glory lily were scarcity of planting material and lack of information on seed dormancy breaking techniques. Even though several treatments like cold and hot water soaking, acid and mechanical scarification for varying durations have been suggested by several authors (Al-Helal et al., 1989; Thomas, 1994; Revathi, 2001) for different crops, none of the treatments were tried to over come seed dormancy in glory lily. Keeping this in view, the present investigation was carried out. Materials and Methods The laboratory experiment was conducted during 2007- 2008 at the Department of Seed Science and technology, Tamil Nadu Agricultural University, Coimbatore to optimize the seed dormancy breaking treatment in glory lily. Five dormancy breaking treatments were imposed with a control. The experiment was laid out in three replications. For hot water soaking treatments, the seeds were soaked in boiled water (100°C) immediately after removing the water from flame for different durations. In H2SO4 scarification treatments, the seeds were scarified with commercial sulphuric acid for different durations. Immediately after scarification, the seeds were washed with water thoroughly. After the treatments, the seeds were placed for germination in petri-plates to record the speed of *Corresponding author

germination (Maguire, 1962). The seed germination test was conducted in roll towel method and the observations were recorded on germination percentage, root and shoot length, seedling dry matter, vigour index, abnormal seedlings, hard seeds and dead seeds percentage (ISTA, 1999). Results and Discussion In the present investigation, the seeds of glory lily soaked in boiled water (100oC) for 40 minutes recorded the highest germination of 62 per cent accompanied with faster rate of germination (4.23), higher seedling length (27.1 cm), dry matter production (181 mg seedlings -10) and vigour index (1680), compared to control seeds (22% germination) (Table 1). The higher seed germination due to soaking in hot water might be due to the weakening of seed coat by distributing and dissolving the lignins and pectins present on epidermal layer of the seed coat, which render them impermeable to water and oxygen. However, hot water soaking treatment for less than 40 minutes duration is ineffective as it could be seen from the higher percentage of hard seed (36 %) at the end of germination test. In contrast, longer period of treatment beyond 40 minutes was harmful as it could be seen from the production of more abnormal seedlings (24 %) and dead seeds (27 %), even though the hard seed content was minimum (8 %) at the end of germination test (Table 2). These results are in agreement with the findings of Kumari and Kohli (1984), Mehta and Sen (1991) and Kalavathi (1996) in Cassia angustifolia and Sivakumar (2005) in Abelmoschus moschatus

32 Table 1. Effect of dormancy breaking treatments on speed of germination, germination, seedling length and dry matter production in glory lily Treatment

Speed of Germination (%)

T0 - Control (untreated) T1 - Soaking in hot water for 20 min. T2 - Soaking in hot water for 40 min. T3 - Soaking in hot water for 60 min. T4 - Scarification with H2SO4 for 2 min T5 - Scarification with H2SO4 for 4 min T6 - Scarification with H2SO4 for 6 min Mean SEd CD(P=0.05)

2.65 4.19 4.23 4.02 4.14 4.13 3.82 2.26 0.086 0.178

Germination (%) 22 (27.9) 46 (42.70) 62 (51.94) 41 (39.81) 52 (46.14) 46 (42.14) 40 (39.23) 44 (41.63) 0.787 1.688

Root length (cm)

Shoot length Dry matter (cm) production (mg seedlings -10)

12.7 14.5 16.1 13.8 15.0 14.9 13.2 8.35 0.323 0.667

8.1 10.7 11.0 10.6 10.9 9.6 9.8 5.89 0.228 0.471

149 166 181 160 179 158 152 95.41 3.761 7.763

(Figures in parentheses are transformed values)

Though acid scarification of seeds with concentrated H2SO 4 for 2 minutes improved the germination (52 %) over non-scarified seeds (22 %), development of abnormal seedlings (14 %) and dead seeds (12 %) were noticed to an increased

level, which might be due to the injury caused to the embryo by the acid as reported by Al-Helal et al., (1989). Similar results on the effect of sulfuric acid treatment have been reported in several temperate and subtropical species. (Willan, 1985). This study

Table 2. Effect of dormancy breaking treatments on vigour index, abnormal seedling production, hard and dead seed contents in glory lily Vigour

Treatment

index T0 - Control (untreated) T1 - Soaking in hot water for 20 min. T2 - Soaking in hot water for 40 min. T3 - Soaking in hot water for 60 min. T4 - Scarification with H2SO4 for 2 min T5 - Scarification with H2SO4 for 4 min T6 - Scarification with H2SO4 for 6 min Mean SEd CD(P=0.05)

458 1159 1680 1000 1347 1127 920 1098.71 0.770

Abnormal seedlings (%) 10 12 14 24 14 16 19 15.57

(18.43) (20.26) (21.97) (29.33) (21.97) (23.57) (25.84) (23.24) 0.359

Hard seed (%)

68 (55.55) 36 ( 36.87) 15 (22.78) 8 (16.43) 22 (27.97) 20 (26.56) 17 (24.35) 26.57 (31.02) 0.744 1.597

Dead seeds (%) 0 (0.62) 6 (14.17) 9 (17.45) 27 (31.30) 12 (20.26) 18 (25.10) 24 (29.33) 13.71 (21.73) 0.329 0.707

(Figures in parentheses are transformed values)

clearly concluded that, soaking the glory lily seed in boiled water (100o for) 40 minutes had substantially improved the seed germination (62%) accompanied with longer seedlings production, dry matter production and vigour index (1680). References Al-Helal, A.A., A-Farraj, M.M. and Ael-desoki, R. 1989. Germination response of senna seeds to sodium salt and temperature. J. Univ. Kuwait Sci., 16: 281-287. ISTA. 1999. International Rules for Seed Testing. Seed Sci. & Technol., (Supplement Rules), 27: 25-30. Kalavathi, D. 1996. Seed production, processing, testing and storage studies in medicinal plants of Senna, Periwinkle and Roselle. Ph.D. Thesis, Tamil Nadu Agricultural University, Coimbatore. Kumari, A. and Kohli, R.K. 1984. Studies on dormancy and macromolecular drifts during germination in Cassia occidentalis L. seeds. J. Tree Sci., 3: 111-125. Maguire, J.D. 1962. Speed of germination aid in selection and evaluation of seedlings emergence and vigour. Crop Sci., 2: 176-177.

Mehta, M. and Sen, D.N. 1991. Seed germination studies of Cassia Italia in Indian desert. Annals of Arid Zone, 30: 67-70. Paramasivam, P. and Arumugam, R. 1991. Survey of Gloriosa superba L. cultivation- a preliminary report. Proceedings of Scientific workers conference, 24-25 July, 1991, Tamil Nadu Agricultural University, Coimbatore. Revathi, R. 2001. Seed production, testing and storage studies in Phyllanthus amarus (Schum & Thom.). M.Sc. (Ag.) Thesis, Tamil Nadu Agricultural University, Coimbatore. Ridley, H.N. 1924. The flora of the Malay peninsula L. Reeves & Co. Ltd., London. Sivakumar, D. 2005. Seed technological studies in ambrette (Abelmoschus moschatus Medic.). M.Sc. (Ag.) Thesis, Tamil Nadu Agricultural University, Coimbatore. Thomas, G. 1994. A study on germination, growth and metabolism of cassia sophera L. and on the rooting of Spilanthes ciliate. Ph.D. Thesis, Mara Thoma College. Tiruvalla, Kerala, India. Willan, R. L. 1985. A guide to forest seed handling. Food and Agriculture Organization of the United Nations. Rome, Italy.

Received: November 11, 2009; Accepted: February 15, 2010

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tiger lily or tiger claws, is an important medicinal plant of the Tropics (Ridley, 1924). The glory lily is native to both Asia and Africa. Paramasivam and. Arumugam, (1991) reported that major problems in the cultivation of glory lily were scarcity of planting material and lack of information on seed dormancy breaking techniques.

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