Effect of inoculation with VAM fungi at different P levels on flowering parameters of Tagetes erecta L.

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Effect of inoculation with VAM fungi at different P levels on flowering parameters of Tagetes erecta L. G. Swathi 1, B. Hemla Naik 2 1 Department of Floriculture and Landscape Architecture, College of Horticulture, Mudigere, Chikmagalur District, Karnataka (India) 2 University of Agricultural and Horticultural Sciences, Shimoga, Karnataka (India) ABSTRACT In this experiment the VAM fungi viz., Glomus fasciculatum (Thaxter) Gerd. and Trappe, Glomus mossea (Nicol. and Gerd.) Gerd. and Trappe, Glomus intraradices Schenck and Smith. with an un-inoculated control was maintained and three P levels viz., 60, 90, 120 kg ha -1 were tried. The results brought out that marigold responded well to VAM inoculation under field conditions. The least days taken to first flowering was recorded with the inoculation of G. fasciculatum and given P at 60 kg/ ha (30.47 days) as compared to other species of Glomus fungi, the least days taken to 50% flowering was recorded with the inoculation of G. fasciculatum and given P at 90 kg/ ha (48.73 days) as compared to the other species of Glomus fungi and uninoculated control plants with given P at 120 kg/ ha and the maximum flowering duration was recorded with the inoculation of G. fasciculatum and given P at 90 kg/ ha (66.60 days) and it was closely followed by G. mosseae (66.00 days) at the same level as compared to the other species of Glomus fungi and uninoculated control plants. Keywords: Marigold, VAM, phosphorus, Glomus fasciculatum, G. mosseae, G. Intraradices, flowering duration, flower bud initiation. I. INTRODUCTION Marigold (Tagetes erecta L.) belongs to the family Asteraceae and genus Tagetes. The two main popularly grown species in marigold are Tagetes erecta L. and Tagetes patula L. which have their origin in Mexico and South Africa, respectively. Tagetes erecta L. is popularly known as African marigold while Tagetes patula L. as French marigold. There are several other important species viz., Tagetes tenuifolia L. (the striped marigold), Tagetes lucida L. (the sweet scented marigold), Tagetes minuta L. and Tagetes lacera L. Compared to any other flowering annuals, marigold is easily adaptable to various conditions of growing and has fairly good keeping quality. It is propagated by seeds and comes up well in all types of soil. The flowers of these species are generally large in size with bright shades, ranging from yellow to orange and are the best for combination in any flower arrangement. Marigold is grown for cut flowers, making garlands, decoration during pooja and several religious functions, besides its use in landscape gardening. Apart from its significance in ornamental horticulture, it has been valued for other purposes too. The aromatic oil extracted from marigold, is called as tagetes oil. It is used in preparation of high grade perfumes and also as an insect fly repellant.. 336 P a g e

Mycorrhiza literally means fungus root. The fungus obtains photosynthesis from plant, while the plant is able to utilize the network of fungal hyphae, (which effectively act as an extended root system). The uptake of inorganic nutrients by plants is influenced by microorganisms in the rhizosphere. Symbiotic endophytes such as mycorrhizae are examples of microorganisms that are involved in the uptake of vital plant nutrient element, phosphorus. Phosphorus is an important plant macronutrient, making up about 0.2 % of a plant s dry weight. Mycorrhizae are important for plant P acquisition, since fungal hyphae greatly increase the volume of soil that plant roots explore (Smith and Read, 1997). In certain plant species, root clusters (proteoid roots) are formed in response to P limitations. These specialized roots exude high amounts of organic acids (up to 23 % of net photosynthesis), which acidify the soil and chelate metal ions around the roots, resulting in the mobilization of P and some micronutrients (Marschner, 1995). Considering its importance as commercial flower crop, the study on effect of VAM fungi on marigold at different phosphorus levels was initiated. II. MATERIALS AND METHODS A factorial experiment was laid out in Randomised Block Design. There were 12 treatment combinations each three replications. In the present experiment VAM fungi (Glomus fasciculatum, G. mosseae, G. intraradices with an uninoculated control) and three levels of phosphorus (60, 90, 120 kg ha -1 ) were tried in all possible combinations. Treatment details are as follows, Factor I = Mycorrhizal species M 1 - Glomus fasciculatum (Thaxter) Gerd. and Trappe. M 2 - Glomus mossea (Nicol. and Gerd.) Gerd. and Trappe. M 3 - Glomus intraradices Schenck and Smith. M o - Uninoculated control Factor II = Phosphorus levels : 3 (225kg N + 60kg K 2 O as constant) P 1-60 kg P 2 O 5 ha -1 P 2-90 kg P 2 O 5 ha -1 P 3-120 kg P 2 O 5 ha -1 2.1. Treatment Combination Treatment No. Treatment Combination T 1 M 0 P 1 Uninoculation + 60 kg P 2 O 5 ha -1 T 2 M 0 P 2 Uninoculation + 90 kg P 2 O 5 ha -1 T 3 M 0 P 3 Uninoculation + 120 kg P 2 O 5 ha -1 T 4 M 1 P 1 G. fasciculatum + 60 kg P 2 O 5 ha -1 337 P a g e

T 5 M 1 P 2 G. fasciculatum + 90 kg P 2 O 5 ha -1 T 6 M 1 P 3 G. fasciculatum + 120 kg P 2 O 5 ha -1 T 7 M 2 P 1 G. mosseae + 60 kg P 2 O 5 ha -1 T 8 M 2 P 2 G. mosseae + 90 kg P 2 O 5 ha -1 T 9 M 2 P 3 G. mosseae + 120 kg P 2 O 5 ha -1 T 10 M 3 P 1 G. intraradices+ 60 kg P 2 O 5 ha -1 T 11 M 3 P 2 G. intraradices + 90 kg P 2 O 5 ha -1 T 12 M 3 P 3 G. intraradices + 120 kg P 2 O 5 ha -1 2.2 Data collection 2.2.1. Days to flower bud initiation The number of days taken from the date of transplanting to the date of appearance of first flower bud was counted as days to flower bud initiation 2.2.2 Days to 50% of flowering (days) The number of days required for 50 per cent of the plants to produce first flower in each plot was recorded by counting the days from the date of sowing. 2.2.3 Flowering duration (Days) The total number of flowering days was counted from the day of flower bud initiation to the complete cessation of flowering in the plant. III. RESULTS AND DISCUSSION The data on days to flower bud initiation, Days to 50% of flowering and Flowering duration as influenced by inoculation of Glomus fungi at different levels of P is presented in the Table 1. 3.1 Result The interaction effect of inoculation of Glomus fungi and P-fertilization was found to be non-significant on days to flower bud initiation. It was decreased with the increase in P level at 120 kg/ ha in uninoculated control. However, the inoculated plants flowered earlier with given P at 90 kg/ ha. The least days taken to first flowering was recorded with the inoculation of G. fasciculatum and given P at 60 kg/ ha (30.47 days) as compared to other species of Glomus fungi and the uninoculated control plants applied with P at 120 kg/ ha and more days were found to be observed in uninoculated control plants with given P at 60kg/ ha (44.80 days) The interaction effect of inoculation of Glomus fungi and P-fertilization was found to be significant in days to 50% of flowering. It was decreased with the increase in P levels up to 120 kg/ ha uninoculated control. However, the inoculated plants flowered earlier with the given P at 90 kg/ ha. However, the least days taken to 50% flowering was recorded with the inoculation of G. fasciculatum and given P at 90 kg/ ha (48.73 days) as compared to the other species of Glomus fungi and uninoculated control plants with given P at 120 kg/ ha and more days were observed in control plants with given P at 120 kg/ ha (57.20 days). 338 P a g e

The interaction effect of inoculation of Glomus fungi and P-fertilization was found to be significant on flowering duration. It was increased with the increase in P levels up to 120kg/ ha in uninoculated control. However, the inoculated plants had maximum flowering duration with the given P at 90 kg/ha. The maximum flowering duration was recorded with the inoculation of G. fasciculatum and given P at 90 kg/ ha (66.60 days) and it was closely followed by G. mosseae (66.00 days) at the same level as compared to the other species of Glomus fungi and uninoculated control plants. The minimum flower duration was observed in uninoculated control plants with given P at 60 kg/ ha (50.53 days). 3.2 Discussion Glomus fungi influenced the days to flower bud initiation and flowering duration in the inoculated plants. In the present study the plants inoculated with G. fasciculatum flowered significantly earlier and has maximum flowering duration as compared to other species of Glomus fungi and uninoculated control (Figure 1). The same trend was observed in the plants inoculated with G. fasciculatum and given P at 90 kg/ ha (48.73 days and 66.60 days, respectively) as compared to uninoculated control plants applied with P at 120 kg/ ha (57.20 days and 61.47 days, respectively). Kandasamy et al., (1986), observed that the inoculated plants flowered early by 7-10 days. A similar trend was observed by Daft and Okusanya (1973) in petunia. Phosphorus induced early flowering in marigold i. e., lesser number of days to 50 per cent flowering. Delay in flowering due to phosphorus deficiency was observed by Bose and Das (1996) in aster, zinnia and salvia Table 1: Effect of inoculation with VAM fungi at different P levels on flowering parameters of Tagetes erecta L. Treatment Flowering Days to flower Days to 50% duration bud initiation of flowering (days) Mycorrhiza M 0 - Uninoculated control 41.96 56.13 57.16 M 1 - Glomus fasciculatum 35.38 50.80 60.64 M 2 - Glomus mosseae 40.71 52.47 59.62 M 3 - Glomus intraradices 44.40 55.29 52.67 S.Em ± NS 0.03 0.05 C.D. (P=0.05) NS 0.10 0.14 Phosphorus levels (kg/ha) P 1-60 30.53 39.76 39.50 P 2-90 29.64 39.31 46.11 P 3-120 31.21 41.69 43.81 S.Em ± NS 0.03 0.03 C.D. (P=0.05) NS 0.07 0.10 Interaction (MXP) 339 P a g e

Days M 0 P 1 - Uninoculated control + P @ 60 44.80 54.80 50.53 M 0 P 2 - Uninoculated control + P @ 90 40.73 56.40 59.47 M 0 P 3 - Uninoculated control + P @ 120 40.40 57.20 61.47 M 1 P 1 - Glomus fasciculatum + P @ 60 30.47 50.93 52.33 M 1 P 2 - Glomus fasciculatum + P @ 90 36.73 48.73 66.60 M 1 P 3 - Glomus fasciculatum + P @ 120 38.93 52.73 63.00 M 2 P 1 - Glomus mosseae + P @ 60 42.80 52.40 55.13 M 2 P 2 - Glomus mosseae + P @ 90 37.40 49.40 66.00 M 2 P 3 - Glomus mosseae + P @ 120 41.93 55.60 57.73 M 3 P 1 - Glomus intraradices + P @ 60 44.73 53.93 52.67 M 3 P 2 - Glomus intraradices + P @ 90 43.20 55.13 53.87 M 3 P 3 - Glomus intraradices + P @ 120 45.20 56.80 51.47 S.Em ± NS 0.10 0.14 C.D. (P=0.05) NS 0.30 0.41 Days to 50% of flowering Flowering duration (days) 70 60 50 40 30 20 10 0 M0P1 M0P2 M0P3 M1P1 M1P2 M1P3 M2P1 M2P2 M2P3 M3P1 M3P2 M3P3 Interaction Figure 1: Effect of inoculation with VAMfungi at different P levels on flowering parameters of Tagetes erecta L. M 0 - Uninoculated control M 1 - Glomus fasciculatum M 2 - Glomus mossae M 3 - Glomus intraradices P 1 60 kg P 2 O 5 ha -1 P 2 90 kg P 2 O 5 ha -1 P 3 120 kg P 2 O 5 ha -1 340 P a g e

IV.CONCLUSION The least days taken to first flowering, the least days taken to 50% flowering and maximum flowering duration were recorded with the inoculation of G. fasciculatum and given P at 90 kg/ ha (36.73, 48.73, 66.60 days, respectively) as compared to uninoculated plants supplied with P at 120 kg ha -1. This indicates the possibility of reducing P fertilizer application by 25 % of the recommended dose to marigold by inoculation with a suitable strain of VAM fungi, i. e., G. fasciculatum and G. mosseae. REFERENCES [1.] MARSCHNER, H., 1992, Mineral nutrition of higher plants. 2 nd edition. Academic press, San Diego. pp.889. [2.] *KANDASAMY, D., OBLISAMY, G., MOHANDOSS, S. AND SHANTHANAKRISHNAN, P., 1986, Influence of VA mycorrhizal inoculation on the growth of pyrethrum in the nursery. Pyrethrum Post, 16(3): 81-83. [3.] BOSE, T. K. AND DAS, S. M., 1996, Studies on the nutrition of ornamental plants. Effects of NPK on growth and flowering of Aster, salvia and Zinnia. Indian Journal of Horticulture, 23: 88-97. [4.] DAFT, M. J. AND OKUSANYA, B. O., 1973, Effect of Enodogone mycorrhizae on plant growth. VI. Influence of infection on the anatomy and reproduction. New Phytology, 72: 1333-1339. 341 P a g e