Keeping Quality and Vase life of Carnation cv. Eskimo as Influenced by Different Chemicals

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Keeping Quality and Vase life of Carnation cv. Eskimo as Influenced by Different Chemicals Malik Abid Mahmood 1, Ahmad Sattar Khan 2, Naveed Ahmad 1* and Misha Arshad 3 1 Directorate of Floriculture (T&R) Punjab, 21-Davis Road, Lahore, Pakistan 2 Institute of Horticultural Sciences, University of Agriculture, Faisalabad, Pakistan 3 Institute of Agricultural Sciences, Punjab University, Lahore, Pakistan *Corresponding author, s email: nahmad57@gmail.com Present experiment was carried out to check the effect of different concentrations of sucrose (2, 4, 6%), GA3 (25, 50, 75 ppm) and combination of sucrose and CuSO4 (2% + 200, 4% + 300, 6% + 400 ppm), sucrose and GA3 (2% + 25 ppm), (4%+50 ppm), (6%+75 ppm) on keeping quality and vase life of carnation cv. Eskimo. Some postharvest characteristics such as vase life, total soluble solids (TSS), water uptake and quality change were evaluated. The experiment was laid out according to RCD (Randomized Complete Design) with three replications while for quality change it was two factor factorial. Maximum vase life in term of days was recorded in treatment T6 and T13 (8 days) followed by T4 (7.7 days). T5 & T12 were at par (7 days). Maximum water uptake was also observed in T13 (56.7 ml) followed by T6 (49.7 ml) and T8 (45 ml). Maximum TSS were found in T13 (8.3 %) followed by T6, T11 and T12. Keeping quality characteristic of T6 was deteriorated slowly as compared to other treatments. Hence, T6 was found superior in overall respects. Abstract Keywords: Carnation, CuSO4, Eskimo, GA3, Sucrose, Vase life. Journal of Ornamental Plants, Volume 5, Number 1: 15-20, March, 2015 15

INTRODUCTION Carnation a native to Mediterranean region (Salehi, 2006) is an important flower crop having great commercial value as a cut flower due to its excellent keeping quality, wide range of colors and forms (Pralhad, 2009). Carnation flowers are sold as cut flowers round the year throughout the world and it is on the top three cut flowers traded in the international market. The demand for carnation as cut flower is gaining momentum with increasing socio-economic standards of the people. The greatest interest of a florist is to prolong the vase life of the flowers. The appearance of bent neck, wilting of outer petals and yellowing of the leaves indicate the end of the useful vase life of cut flowers (Ketsa and Narkbua, 2001; Reid, 2002). Longevity of vase life is an important factor for consumer preference. Short vase life is one of the most problems of the cut flowers (Kader, 2003). Senescence of cut flowers is induced by several factors e.g water stress (Sankat and Mujaffar, 1994), microorganisms and ethylene effects (Han and Miller, 2003). In cut flowers, poor water availability has been reported as a result of increased stem resistance to water flow resulting from microbial growth and high ph of vase solutions. This problem has been overcome in various cut flowers by the use of bactericide and low ph vase solutions (Nowak and Rundnicki, 1990). As carnation is one of the most important cut flower nowadays as well. Therefore it is important to ensure the longest vase life of the flowers. The postharvest performance and vase life of cut flowers is influenced by flower handling (Pizano, 2009), carbohydrate content, blockage of xylem vessels, ethylene, the composition of the atmosphere, and the chemical solutions of the preservatives. Tap water solution containing low concentration of copper sulphate (50 µm), calcium chloride (0.7 mm) and NaHCO3 (1.5 mm) is appropriate as standardized vase solution as copper ions act as biocide (Halevy and Mayak, 1981; Van Doorn, 1997) and a wound reaction enzyme inhibitor (Vaslier and Van Doorn, 2003). Adding sucrose to the vase solutions improved bud opening and further extended vase life of inflorescences (Van Doorn and Reid, 1992) and sucrose supplies the energy and carbon skeletons required for bud opening. Steinitz and Cohen (1982) found that gibberilic acid was effective in promoting petal expansion. Therefore, this experiment was conducted to check the effect of different chemicals on the enhancement of vase life of carnation. The main objective of the study was to investigate the effect of various concentrations of sucrose, copper sulphate and growth regulators e.g. gibberellic acid on carnation cut flower longevity and quality. MATERIALS AND METHODS The present investigation was carried out to study the effect of chemicals on keeping quality and vase life of carnation. Fresh cut flowers of carnation cv. Eskimo were harvested from a private cut flower farm and were transported to postharvest laboratory, Directorate of Floriculture, Punjab, Lahore, during March 2014. The experiment was conducted in a completely randomized design. There were 12 treatments (Table 1) and each treatment was consisted of ten flowers and each experiment was repeated twice. Prior to treatment, carnation cut flowers were trimmed to equal length and the lower most leaves were discarded. The data on vase life (days), total soluble solids (%), water uptake (ml) and quality change were recorded. Flowers were observed daily till they were found unfit for containing in vase. The vase life was expressed in terms of days from the date of harvesting to final observation (wilting of one third of petals in each flower). In order to measure petal total soluble solids, one cut flower was picked up from each experimental unit and its petals were grinded into a powder. Few drops of petal extract were taken in to a multi-range analyzer Refractometer (ATAGO, RS-5000 Atago, Japan) and TSS value was recorded in Brix. The water uptake was measured in the vases containing 250 ml of solution after eight days. The average of 3 replication values was used in order 16 Journal of Ornamental Plants, Volume 5, Number 1: 15-20, March, 2015

Table 1: Treatment detail of holding solutions. Sr. No. Treatment Details 1 2 3 4 5 6 7 8 9 10 11 12 13 T0 T1 T2 T3 T4 T5 T6 T7 T8 T9 T10 T11 T12 Control (tap water) 2% sucrose 4% sucrose 6% sucrose 2% sucrose+cuso4 200 ppm 4% sucrose+cuso4 300 ppm 6% sucrose+cuso4 400 ppm 25 ppm GA3 50 ppm GA3 75 ppm GA3 2% sucrose + 25 ppm GA3 4% sucrose + 50 ppm GA3 6% sucrose + 75 ppm GA3 to establish evaporation value. Simultaneously the water deficiency was measured in control vase. For each experimental unit water uptake was calculated by subtracting the two above values with each other. Flower quality change was assessed by visual inspection using a 4 grade system (0 = absent, 1 = little, 2 = moderate and 3 = severe). Quality inspection was carried daily and grades were assigned to each treatment. The experimental data were subjected to analysis of variance (ANOVA) using Statistix 9 for windows software. The effects of treatments were determined from the least significant differences test (Fisher s LSD) at P < 0.05, where the F test was significant (Steel et al., 1997). All the assumptions of analysis were checked to ensure validity of statistical analysis. All graphs were drawn using Excel software. RESULTS AND DISCUSSION Vase life (Days) Statistical analysis showed that the treatments responded positively for the enhancement of vase life. Mean comparison showed that T6 (4% sucrose+cuso4 300 ppm) and T13 (6% sucrose + 75 ppm GA3) had maximum vase life (8 days) followed by T4, T5 and T12 while minimum vase life was recorded in T1 (3.7) (Fig. 1). Edrisi et al. (2012) observed CuSO4 as effective chemical to control microbial growth in vase solution. Mahmood et al. (2014) observed same vase life in carnation cv. Tempo. Vase life can be determined by the availability of carbohydrates to carry on physiological activities to assimilate food for keeping the cut flower fresh and long lived. The more are food reserves, the better and longer the days to loose freshness. CuSO4 (300 ppm) was most effective for maintaining quality of carnation flowers. This could be due to the reason that the fungal activities were slower down at this concentration. Fig. 1. Vase life of Carnation Cv. Eskimo as Influenced by Different Chemicals. Journal of Ornamental Plants, Volume 5, Number 1: 15-20, March, 2015 17

Fig. 2. Water intake of Carnation Cv. Eskimo as Influenced by different Chemicals. Water uptake Maximum solution uptake was observed for flower kept in T13 (56.7 ml), T6 (49.7 ml) and T8 (45.0 ml), minimum uptake was recorded in T4 (24.3 ml) followed by T3 (25.3 ml) and T2 (27.7 ml) (Fig. 2). It is observed that CuSO4 and GA3 play effective role in water uptake. Gibberellic acid causes the conversion of starch to sucrose, fructose, and glucose. The accumulation of these reduced sugars produces a lower water potential within the cells and consequently increases WI capability (Mutui et al., 2006). It seems that silver compounds and particles transport throughout stem vascular system and removes pathogenesis infection inside the vascular system and promote WI potential of plants (Ketsa et al., 1981). Total soluble solids In our study maximum soluble solids were observed in T13 (8.3%) followed by T6 (8%), T11 (8%) and T12 (8%). Minimum total soluble solids were observed in T4 (5%) and T5 (4%) (Fig. 3). According to a research, CKs cause assimilates transfer from leaves to developing flower organs and result in TSS increment of flower petals. In Gladiolus cut flowers it was found that treating flowers with100 mg L -1 GA3 increased sugar content in the petals and leaves until 10 days after harvest. Gibberellins could maintain photosynthesis system in cut flower leaves until their yellowing and abscission (Hassanpour-Asil and Karimi, 2010). 18 Fig. 3. Total soluble solids of Carnation Cv. Eskimo as Influenced by Different Chemicals. Journal of Ornamental Plants, Volume 5, Number 1: 15-20, March, 2015

Table 2: Keeping Quality of Carnation Cv. Eskimo as Influenced by Different Chemicals. Treatments Days 1 2 3 4 5 6 7 8 Means T1 T2 T3 T4 T5 T6 T7 T8 T9 T10 T11 T12 T13 Means 0.66 D 0.051H 0.38 G 1.30 F 1.69 E 2.07 D 2.46 C 2.69 B 2.92 A 2.45 A 1.50 E 1.87 C 0.87 H 1.25 G 1.37 F 1.37 F 1.62 D 1.87 C 1.87 C Means in the same column followed by the same letter are not significantly different by LSD test. Quality change As the food reserves are exhausted, symptoms like discoloration and deterioration of quality appear, there are many other factors which also contribute towards quality change like temperature, humidity and the post-harvest handling of flowers. Table 2 depicted that during first day of experiment change of quality only in T1 was observed. Severe change in quality of T1 was observed on fourth day of experiment. Quality of flowers in T6 deteriorated slowly and there was no change in quality was observed up third day in T6. Moderate quality change was observed on 8 th day of experiment in T6. Edrisi et al. (2012) observed that proper dose CuSO4 delayed wilting by inhibiting microbial growth. CONCLUSION The above mentioned findings indicated that considering the important characteristics, T6 and T13 are more effective for prolonging vase life and maintaining quality of carnation cut flowers. Literature Cited Edrisi1, B., Sadrpoor, A. and Saffari, V.R. 2012. Effects of chemicals on vase life of cut carnation (Dianthus caryophyllus L. Delphi ) and microorganisms population in solution. Journal of Ornamental and Horticultural Plants, 2 (1): 1-11. Halevy, A.H. and Mayak, S. 1981. Senescence and postharvest physiology of cut flowers Part 2. Horticultural Review, 3: 59 141. Han, S.S. and Miller, J.A. 2003. Role of ethylene in postharvest quality of cut oriental lily Stargazer. Plant Growth Regulation, 40: 213-222. Hassanpour-Asil, M. and Karimi. M. 2010. Efficiency of benzyladenine reduced ethylene production and extended vase life of cut Eustoma flowers. Plant Omics Journal. 5:199-203. Kader, A.A. 2003. A perspective on postharvest horticulture. Journal of Horticaltural Science, 38: 1004-1008. Ketsa, S. and Narkbua, N. 2001. Effects of amino oxyacetic acid and sucrose on vase life of cut roses. Acta Horticulturae. 543: 227-234. Ketsa, S., Tongumpai, P. and Siripanich. T. 1981. Effect of silver thiosulfate pretreatment on vase life of cut carnation flowers. Kasetsart Journal. 21: 207-213. Mahmood, M.A., Khan, M. S. A. and Ahmad, N. 2014. Growth, yield and quality of carnation (Dianthus caryophyllus L.) cultivars under lath house conditions. Journal of Ornamental Plants, Volume 4, Number 1: 27-32. Mutui, T.M., Emongor, V.E. and Hutchinson. M.J. 2006. Effect of gibberellin on the vase life and Journal of Ornamental Plants, Volume 5, Number 1: 15-20, March, 2015 19

flower quality of Alstroemeria cut flowers. Plant Growth Regulation. 48(3): 207-214. Nowak, J. and Rudnicki, R. 1990. Postharvest and storage of cut flowers, florist green and potted plants. P. 210. Timber Press, Inc., Oregon USA. Pizano, M. 2009. Research show the way for postharvest treatment roses. Flower Technology, 12(6): 1-13. Pralhad, G.C. 2009. Evaluation of carnation (Dianthus caryophyllus L.) varieties under greenhouse condition. M.Sc. Thesis, Dept. Horti., Univ. Agri. Sci., Dharwad. Reid, M.S. 2002. Non metabolized cytokinins as growth regulators in postharvest performance of ornamentals. Journal of American Society of Horticultural Sciences, 469: 201-205. Salehi, H. 2006. Can a general shoot proliferation and rooting medium be used for a number of carnation cultivars? African Journal of Biotechnology, 5(1): 25-30. Sankat, C. K. and Mujaffar, S. 1994. Water balance in cut anthorium flowers in storage and its effect on quality. Acta Horticalturae, 368: 723-732. Steel, R.G.D., Tomle, J.H. and Dickey, D.A. 1997. Principles and procedures of statistics a biochemical approach. 3 th Ed. McGraw Hill Book Co., Inc., USA. Steinitz, B. and Cohen, A. 1982. Gibberellic acid promotes flower bud opening on detached flower stalks of statice (Limonium sinuatum L.). Hort Science, 17:903 904. Van Doorn, W.G. 1997. Water relations of cut flowers. Horticultural Review, 18: 1 85. Van Doorn, W.G. and Reid, M.S. 1992. Role of ethylene in flower senescence of Gypsophila paniculata L. Postharvest Biology and Technology, 1:265 272. Vaslier, N. and van Doorn, W.G. 2003. Xylem occlusion in Bouvardia flowers: Evidence for a role of peroxidase and cathechol oxidase. Postharvest Biology and Technology, 28: 231 237. 20 Journal of Ornamental Plants, Volume 5, Number 1: 15-20, March, 2015