Study on Purple Nutsedge (Cyperus rotundus) Tuber Dormancy and its Control Through Combined Application of Growth Regulator and Herbicides

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Research Article Study on Purple Nutsedge (Cyperus rotundus) Tuber Dormancy and its Control Through Combined Application of Growth Regulator and Herbicides D. Ravisankar* and C. R. Chinnamuthu Department of Agronomy, Tamil Nadu Agricultural University, Coimbatore - 641 003, Tamil Nadu, India Abstract Laboratory experiments were conducted to study the purple nutsedge tuber dormancy and assessment of combined application of growth regulators along with herbicides for its early growth control. In experiment-1, tuber dormancy study was carried out in two methods viz., selection of different size of the tubers by its weight (0.25g to >1g) and depth of burial in soil from 5cm to 30cm. In experiment-2, application of 0.01% cytokynin along with the effective herbicides viz., Glyphosate, Metolachlor and Almix (Met Sulfuran Methyl + Chloromuran ethyl) in two ways by tank mix application and followed by application. The experiment findings indicated that thecombined application herbicides (Metolachlor 2.5 kg ha -1 ) and growth regulator (0.01 % Cytokinin) as tank mix provided effective control of purple nutsedge. Application Glyphosate @ 3.0 kg ha -1 third day after sprouting induced by the cytokine (0.01 per cent) provided 92 per cent control. Keywords: Purple nutsedge, Tuber dormancy, Cytokynin, Herbicides *Correspondence Author: D. Ravisankar Email: ravi.agri@gmail.com Introduction Purple nutsedge is considered one of the worst weed of the world. Widely distributed throughout the tropics and subtropics in 52 different crops and in 92 countries [1]. Lowering in crop yields is one of the greatest impacts of this species. Purple nutsedge is so highly competitive and causes yield reductions of various crops ranging from 23-89 per cent [2]. Reducing the effect of perennial weeds in crop production systems begins with minimizing reproductive plant propagules (e.g., bud, suckers, seeds and tubers) that are produced and returned to the soil. Cultural practices such as crop rotation and cultivation [3] and soil desiccation [4], do not provide sufficient control of this weed. Purple nutsedge has proved difficult to control with herbicides. Chemical control measures provide only poor or temporary control [5], because of limited uptake and translocation of herbicides, and to temporal inhibition of tuber sprouting [6]. All the commercial herbicides available in the market aimed to control or kill the growing above ground part of the weed plants. The development of dormant tubers enables nutsedge to adopt to various cultural and cropping methods, thus making eradication of this weed difficult. Black tubers exhibit the greatest of dormancy, while young, white tubers sprout easily. Dormant tubers have one to 13 buds. Only few buds will sprout under suitable conditions, the others remaining buds were in dormant condition. Apical buds inhibit sprouting of other buds on the same tuber [7]. Similarly experimental research result noted that, upon the death of the foliage of the growing plant, inhibition of tuber sprouting was relieved and sprouting of tuber buds occurred. Dissecting tubers also stimulated sprouting of dormant buds near the cut surface [8]. Lacking of scientific information regarding physiological and ecological aspects of tuber sprouting is creating difficulty in nutsedge control, which determines to a large extent the potential degree of infestation. The prediction of purple nutsedge tuber sprouting could provide an estimate of the tuber reservoir relative to emerged plants, upon which appropriate decisions for management strategies may be imposed. The understanding of tuber dormancy is important and a prelude to devising effective control method for this world worst weed. One approach for an effective control is to stimulate all buds in the tubers to sprout. The search for an effective method of nutsedge control continues from long back. The use of growth regulators has been suggested as a means to precondition of nutsedge tuber for its early control. It is only after the dormant buds have sprouted and formed shoots that an herbicide may be used effectively on the vegetative parts. After the tubers are exhausted of their viable buds, no rejuvenation of shoots is expected. Much work has been done to control the purple nutsedge through sprouted above ground plant parts. This Chem Sci Rev Lett 2017, 6(22), 727-731 Article CS162048033 727

experiment aims to study the dormancy behavior of the tuber and its control by combined application of growth substances along with herbicides. Materials and Methods Tubers of purple nutsedge were collected in bulk from farmers filed (11 16'42" N 77 35'1" E), and used as the base material for the study. Experiment-I: Influence of depth of burial on tuber dormancy The tubers collected from field were treated with 0.01 per cent cytokinin and were buried into different depths ranged from 5 cm to 30cm at six levels (5 cm each) containing 20 tubers each in pots filled with field soil along with untreated tubers. Similarly different sizes of the tuber were selected based on the weight from less than 0.25g to more than1.0 g. The experiments were laid out in FRBD design in three replications. The pots were watered regularly and the tuber and seedling characters were recorded 30 days after sowing. Experiemnt-II: Influence of combined application of growth regulator and herbicides on purple nutsedge tuber sprouting One set of tubers were treated with 0.01 per cent cytokynin and herbicides with various rates viz., Glyphosate (2.5kgha -1 and 3.0 kgha -1 ), Metolachlor (1.5kgha -1 and 2.0 kgha -1 ) and Almix (4 gha -1 and 6 gha -1 ) similarly another set of tubers were treated with 0.01 per cent cytokynin alone and allowed to sprout and spray the same set of herbicides. The experiments were laid out in FCRD design in three replications Tuber viability was calculated by the tubers collected from each treatment and replication after the sprouting / germination period were given with a longitudinal cut and soaked in 1.0 per cent tetrazolium chloride solution and kept at 40 0 C for 6 h. The tubers were then rinsed thoroughly with water and were examined by staining. The stained and unstained tubers were counted and the mean expressed in percentage to the total tubers placed for germination. The germination percentage and other growth parameters was calculated Results and Discussion Influence of depth of burial and size of the tuber on tuber germination and growth The tubers buried at different depths of soil significantly influenced the tuber sprouting and growth characters of purple nutsedge. Highly significant differences were obtained among the different depth of burial of tubers and tuber treatments (tubers treated with 0.01 and control) for the tuber characters viz., germination, dormancy and vigour index. However, the interaction effects between the treatments and different depth of burial were non significant. As evident from the Table 1, the germination percentage was decreased with increasing the depth of burial of tubers. Among the depth of burial, 5 cm was recorded the maximum germination of 77 per cent, followed by 10, 15, 20 and 25 cm viz., 72, 69, 64 and 56 per cent respectively. The minimum sprouting was recorded in 30 cm depth (51 per cent). Between the treatments, tubers treated with 0.01 per cent cytokinin recorded the maximum germination percentage (76 per cent), while untreated tubers recorded the minimum germination percentage (53 per cent).the interaction effects between the depth of burial of tubers and dormancy breaking treatments were non significant. The maximum value of vigour index (2688) was obtained with the depth of burial of tubers at 5 cm, and was followed by 10, 15, 2 and 25 cm depths attained the values viz., 2522, 1890, 1401 and 1058 respectively. The minimum vigour index value was recorded with 30 cm depth (867). Dormancy breaking cytokinin treatment imposed tubers recorded the highest value of vigour index (2099), while untreated tubers recorded the lowest value (1376). Interaction effect due to depth of burial and cytokinin treatments were non significant (Table 1). The similar results were found with earlier research experiments [9]. Influence of size of tuber on its germination and growth Significant difference in germination percentage was noticed between different size of tubers and cytokinin treatments (Table 2). Among the different size of tubers, 0.5-75 g was recorded the maximum germination percentage (78 per cent), followed by 0.25-0.50, more than 1 and 0.75-1 g recorded 75, 74 and 72 per cent respectively. Minimum Chem Sci Rev Lett 2017, 6(22), 727-731 Article CS162048033 728

sprouting was recorded with less than 0.25 g sized tubers (71 per cent). Between the treatments, tubers treated with 0.01 per cent cytokinin recorded the maximum sprouting (87 per cent), while untreated tubers recorded the minimum sprouting (61 per cent). The interaction effect between the different size of the tubers was non significant. Table 1 Influence of depth of burial on tuber germination and vigour index of purple nutsedge Depth of burial (D) Treatment (T) Germination (%) Vigour index (cm) Untreated Treated 0.01 Mean Untreated Treated 0.01 Mean 5 64 (53.55) 89 (70.80) 77 (62.17) 2154 3222 2688 10 60 (50.81) 83 (65.96) 72 (58.39) 2013 3031 2522 15 56 (48.07) 81 (63.92) 69 (56.00) 1491 2290 1890 20 53 (46.92) 75 (59.81) 64 (53.35) 1094 1709 1401 25 46 (42.51) 66 (54.14) 56 (48.32) 822 1295 1058 30 39 (38.84) 62 (51.95) 51 (45.40) 684 1050 867 Mean 53 (46.79) 76 (61.10) - 1376 2099 - D T D X T D T D X T SEd 1.35 0.78 1.91 107 62 152 CD(P =5 %) 2.80 1.62 NS 223 129 316 Table 2 Influence of size of tuber on germination and vigour index of purple nutsedge Tuber Size (S) (g) Treatments (T) Germination (%) Vigour index Untreated Treated 0.01 % cytokinin Mean Untreated Treated 0.01 Mean < 0.25 55 (47.68) 86 (70.62) 71 (66.26) 1227 2272 1750 0.25 0.50 61 (51.16) 90 (71.81) 75 (69.89) 1656 2677 2166 0.50 0.75 65 (53.54) 91 (73.21) 78 (72.15) 1916 3145 2531 0.75 1.00 60 (50.77) 83 (65.60) 72 (66.17) 1980 2886 2433 > 1.00 64 (52.94) 84 (66.48) 74 (68.28) 2255 2934 2595 Mean 61 (51.22) 87 (69.54) - 1807 2783 - S T S X T S T S X T SEd 2.887 1.826 4.083 233 147 328 CD (P =5 %) NS 3.837 NS 489 309 NS The maximum value of vigour index (2595) was recorded with the tuber weighing more than 1 g and was followed by 0.5-75, 0.75-1, 0.25-0.5 g viz., 2531, 2433 and 2166 respectively (Table 2). The lowest vigour index value of 1750 was recorded less than 0.25 g weighing tubers. Among the treatments, 0.01 per cent cytokinin treated tubers recorded the maximum value of vigour index (2783), compared to untreated tubers (1807). Similar result was recorded in yellow nutsedge tuber [10]. Experiment-II: Pre-emergence control of purple nutsedge using growth promoting substance and herbicides Sprouting control and viability reduction (tank mix application) The data associated with the effect of combined application of 0.01 per cent cytokinin and herbicides with different concentration levels as tank mix under different germination media on nutsedge tuber sprouting control and viability reduction is presented in the Table 3. It was observed that the tank mix application of 0.01 per cent cytokinin with different herbicides significantly reduced the viability and sprouting of purple nutsedge. Higher sprouting control of 100 per cent was recorded with metolachlor @ 2.0 kg ha -1 and metolachlor @ 1.5 kg ha -1. The minimum control of 93 per cent was recorded with almix @ 4 g ha -1 and almix @ 6 g ha -1. In the case of viability reduction metolachlor @ 2.0 kg ha -1 recorded the maximum percentage of 95. The minimum viability reduction (71 per cent) recorded with almix @ 4 g ha -1. Application of 0.01 per cent cytokinin and metolachlor @ 2.0 kg ha -1 in the paper media recorded one hundred per cent reduction in the viability of purple nutsedge followed by 96 percent with 0.01 per cent cytokinin + metolachlor Chem Sci Rev Lett 2017, 6(22), 727-731 Article CS162048033 729

@ 1.5 kg ha -1. In earlier studies also shows that that 99 % of the tubers had viability up to 42 months and also the higher amount of stored energy is responsible for vigours growth and fast reproduction of the plant after emergence [11]. Table 3 Effect of combined application of growth regulator and herbicides on tuber viability Treatments Tank mix application Followed by application Sprouting control (%) Viability reduction (%) Foliage control (%) Viability reduction (%) T 1 Glyphosate @ 2.5 kg ha -1 92 75 100 78 T 2 Glyphosate @ 3.0 kg ha -1 94 78 100 84 T 3 - Metolachlor @ 1.5 kg ha -1 100 86 92 76 T 4 Metolachlor @ 2 kg ha -1 100 90 100 80 T 5 Almix @ 4 g ha -1 86 68 70 64 T 6 Almix @ 6 g ha -1 86 72 74 73 Mean 93 78 89 76 Foliage control and viability reduction (followed by application) Maximum foliage control of 100 per cent was recorded with glyphosate @ 2.5 kg ha -1, glyphosate @ 3 kg ha -1 and metolachlor @ 2.0 kg ha -1. The minimum foliage control (77 per cent) was recorded with almix @ 4 g ha -1. In the case of viability reduction maximum percentage of 88 per cent was recorded with glyphosate @ 3.0 ka ha -1.Application of 0.01 per cent cytokinin and glyphosate @ 3.0 kg ha -1 in the paper media recorded 92 per cent reduction in the viability of purple nutsedge followed by 87 per cent with 0.01 per cent cytokinin followed by application of glyphosate @ 2.5 kg ha -1. This may be attributed that glyphosate, a post-emergence non selective systemic herbicide, might have influenced one hundred per cent on the growing sprouts and reduced the viability of tubers. Conclusion Tuber germination did not influenced significantly by the tuber weight. Combined application herbicides (Metolachlor 2.5 kg ha -1 ) and growth regulator (0.01 per cent cytokinin) as tank mix provided effective control of purple nutsedge. Application glyphosate @ 3.0 kg ha -1 third after sprouting induced by the cytokine (0.01 per cent) provided 92 per cent control. Chem Sci Rev Lett 2017, 6(22), 727-731 Article CS162048033 730

References [1] Charles,G.W. Herbicidal strategies for reducing nutsedge (Cyperus rotundus L.), Aust. J. Exptl. Agric., 1997, 37(2):231-141. [2] Bryson, C.T., K. Reddy and W.T. Molin. Purple nudsedge (Cyperus rotundus L.) population dynamics in narrow transgenic cotton (Gossypium hirsutum L.) and Soybean (Glycine max) rotation, Weed Tech., 2003, 17(4): 805-810. [3] Glaze, N.C. Cultural and mechanical manipulations of Cyperus spp., Weed Tech., 1987, 1:82-3. [4] Horowitz, M. Growth, tuber formation and spread of Cyperus rotundus L. from single tubers, Weed Res., 1972, 12: 348 363. [5] Pereira, W., G. Crabtree and R.D. William. Herbicide action on purple and yellow nutsedge (Cyperus rotundus L. and C. escidentia L.), Weed Tech., 1987, 1:92-8. [6] Kleifeld, Y., T. Buimenfeld., G. Herzlinger and H. Bucsbalm. Control of purple nutsedge (Cyperus rotundus L.) in cotton with benfuresate, Phytoparasitica, 1992, 20:37-46. [7] Ueki, K. Studies on the control of nutsedge (Cyperus rotundus L.) on the germination of a tuber, In: Proc. Asian-Pacific Weed Sci. Soc. Conference., 1969, 2:355 369. [8] Jangaard N.O., M.M. Sckerl and R.H. Schieferstein. The role of phenolics and abscisic acid in nutsedge tuber dormancy, Weed Sci., 1971,19: 17-20. [9] Gilreath, J.P. and B.M. Santos. Herbicide dose and incorporation depth in combination with 1,3- dichloropropene plus chloropicrin for Cyperus rotundus control in tomato and pepper, Crop Prot., 2004, 23: 205-210. [10] Stoller, E.W., D.P. Nema and W.M. Bhan. Yellow sedge tuber germination and seedling development, Weed Sci., 1972, 12:3-97. [11] Neeser, C., R.Aguero and C.J. Swanton. Survival and dormancy of purple nutsedge Cyperus rotundus L.) tubers, Weed Sci., 1997, 45:784 790. 2017, by the Authors. The articles published from this journal are distributed to the public under Creative Commons Attribution License (http://creative commons.org/licenses/by/3.0/). Therefore, upon proper citation of the original work, all the articles can be used without any restriction or can be distributed in any medium in any form. Publication History Received 16 th Mar 2017 Revised 05 th Apr 2017 Accepted 06 th Apr 2017 Online 30 th Apr 2017 Chem Sci Rev Lett 2017, 6(22), 727-731 Article CS162048033 731