versión On-line ISSN 0718-5839
Chilean J. Agric. Res. vol.71 no.2 Chillán jun. 2011
Chilean Journal of Agricultural Research 71(2) April-June
RESEARCHOvicidal effect of some insecticides on the diamondback moth, Plutella xylostella (L.) (Lepidoptera: Yponomeutidae)
Efecto ovicida de algunos insecticidas sobre la polilla del repollo, Plutella xylostella (L.) (Lepidoptera: Yponomeutidae).
Mohammad Mahmoudvand1*, Aziz Sheikhi Garjan2, and Habib Abbasipour3
1Islamic Azad University, Department of Plant Protection, Khorramabad Branch, Khorramabad, Iran. *Corresponding author (email@example.com).
2Iranian Research Institute of Plant Protection,
3Department of Plant Protection, Faculty of Agricultural Sciences, Shahed University, Tehran, Iran.
The diamondback moth, Plutella xylostella (Lepidoptera: Yponomeutidae), is a serious threat to Brassica vegetables in Iran, including Tehran province. The ovicidal effects of different classes of insecticides on P. xylostella were investigated, using three fixed doses (based on commercial formulations). At the lowest concentration (500 mg L-1), the mortality effect of hexaflumuron and pyridalyl was higher than the other insecticides examined. Fipronil, hexaflumuron and spinosad and pyridalyl, however, showed high toxic effects at the median dose (1000 mg L-1). On the other hand, at high concentration (2000 mg L-1), all insecticides except lufenuron and indoxacarb (EC formulation) caused more than 85% mortality. Overall, these findings indicate that hexaflumuron, spinosad and fipronil, with low active ingredients and high mortality, could be the best choices for controlling the P. xylostella in the egg stage.
Key words: diamondback moth, Plutella xylostella, insecticides, ovicidal effect.
La polilla del repollo, Plutella xylostella (L.) (Lepidoptera: Yponomeutidae), es un serio riesgo para especies Brassica en Irán, incluyendo la provincia de Teherán. Se investigó el efecto ovicida de algunos insecticidas pertenecientes a diferentes clases de P. xylostella usando tres dosis (basadas en formulaciones comerciales). A la menor concentración (500 mg L-1) el efecto de mortalidad de hexaflumuron y piridalil fue mayor que las otras dosis examinadas. Fipronil, hexaflumuron spinosad y piridalil, sin embargo, mostraron fuertes efectos tóxicos a la dosis media (1000 mg L-1). Por otra parte, a alta concentración (2000 mg L-1) todos los insecticidas excepto lufenuron e indoxacarb (formulación EC) causaron más de 85% mortalidad. Finalmente, estos hallazgos indican que hexaflumuron, spinosad y fipronil con baja concentración de ingredientes activos y alta mortalidad pueden ser la mejor elección para controlar P. xylostella en el estado de huevo.
Palabras clave: polilla del repollo, Plutella xylostella, insecticidas, efecto ovicida.
The diamondback moth, Plutella xylostella (Lepidoptera: Yponomeutidae), is the most destructive pest of brassicaceae in the world and a serious problem in Iran. Its global importance is reflected by the fact that almost US$1 billion is spent annually on its control (Talekar and Shelton, 1993; Mahmoudvand et al., 2009). Although chemical control is the most conventional method against the diamondback moth, resistance to insecticides has developed in P. xylostella (Sun et al., 1986; Shelton et al., 1991).
Insect growth regulators (IGRs) are a unique class of insecticides with selective effects on various life stages of some orders of insects. They interrupt molting (juvenile hormone or ecdysone mimics) and cuticle formation (chitin synthesis inhibitors) and affect the insect endocrine system (Dhadialla et al., 1998; Hoffmann and Lorenz, 1998). Chitin synthesis inhibitors (CSI), a group of IGRs, are benzoylphenylurea (BPU) with high specificity, low mammalian toxicity and rapid degradation in the environment. These compounds are effective on immature stages of insects (Mian and Mulla, 1982; Reynolds, 1987). Hexaflumuron (1-[3,5-dichloro-4-(1,1,2,2-tetrafluoroethoxy)phenyl]-3-(2,6-difluorobenzoyl)urea), which is a CSI, has been used to control a wide range of agricultural pests. It has ingestion, contact and ovicidal toxicity (Sbragia et al., 1983; Su and La Fage, 1987). Lufenuron ((RS)-1-[2,5-dichloro-4-(1,1,2,3,3,3-hexafluoropropoxy)phenyl]-3-(2,6-difluorobenzoyl)urea), another IGR, is employed to control the lepidopteran and coleopteran larvae on vegetable and cotton crops (Mossan et al., 1995). Fipronil ((5-amino-1-[2,6-dichloro-4-(trifluoromethyl)phenyl]-4-(trifluoromethylsulfinyl)-1H-pyrazole-3-carbonitrile) has a unique mode of action and interferes with the passage of chloride ions through the gamma-aminobutyric acid (GABA) regulated chloride channel (Cole et al., 1993). Spinosad (mixture of 50-95% of (2R,3aS,5aR,5bS,9S,13S,14R,16aS,16bR)-2-(6-deoxy-2,3,4 -tri-O-methyl-α-L-mannopyranosyloxy)-13-(4-dimethylamino-2,3,4,6-tetradeoxy-β-D-erythropyranosyloxy)-9-ethyl-2,3,3a,5a,5b,6,7,9,10,11,12,13,14,15,16a,16b-hexadecahydro-14-methyl-1H-as-indaceno[3,2-d]oxacyclododecine-7,15-dione and 50-5% of (2S,3aR,5aS,5bS,9S,13S,14R,16aS,16bS)-2-(6-deoxy-2,3,4-tri-O-methyl-α-L-mannopyranosyloxy)-13-(4-dimethylamino-2,3,4,6-tetradeoxy-β-D-erythropyranosyloxy)-9-ethyl-2,3,3a,5a,5b,6,7,9,10,11,12,13,14,15,16a,16b-hexadecahydro-4,14-dimethyl-1H-as-indaceno[3,2-d]oxacyclododecine-7,15-dione), is a selective insecticide based on a fermentation product of the soil bacterium actinomycete (Saccharopolyspora spinosa), which was discovered in the 1980s (Mertz and Yao, 1990; Miles and Dutton 2000; Crouse et al., 2001). Pyridalyl (2,6-dichloro-4-(3,3-dichloroallyloxy) phenyl 3-[5-(trifluoromethyl)-2-pyridyloxy] propyl ether), which is a new synthetic insecticide, was discovered at Sumitomo Chemical Co. Ltd., Japan. This insecticide has contact and ingestion toxic effects and is excellent for controlling lepidopteran and thysanopteran pests (Sakamoto et al., 2003; Saito et al., 2004). Indoxacarb (methyl(S)-N-[7-chloro-2,3,4a,5-tetrahydro-4a-(methoxycarbonyl)indeno[1,2-e][1,3,4]oxadiazin-2-ylcarbonyl]-4-(trifluoromethoxy)carbanilate or methyl (S)-7-chloro-2,3,4a,5-tetrahydro-2-[methoxycarbonyl(4-trifluoromethoxyphenyl)carbamoyl]indeno[1,2-e][1,3,4]oxadiazine-4a-carboxylate) has a good toxic effect as an oxadiazine insecticide against lepidopteran pests with no effect on non-target insects. This insecticide causes the lepidopteran larvae to stop feeding. It also results in irreversible convulsions and severe paralysis (Wing et al., 1998; Dinter and Wiles, 2000). Indoxacarb affects the target insects by blocking the sodium channels of nerve cells (Meier et al., 1992).
Brassica vegetables are important vegetable crops grown throughout Tehran province and other areas of Iran. P. xylostella occurs annually throughout Tehran fields, wherever brassicaceous crops are grown, and causes substantial crop losses, especially during outbreak years. To our knowledge, no insecticides for diamondback moth control in Iran have been investigated. This is the first study to show the toxicity of insecticides on P. xylostella eggs. In the field, insecticides are usually applied in their commercial formulation. Thus, the aim of this research was to compare the ovicidal property of some insecticides (spinosad, indoxacarb EC, indoxacarb SC, pyridalyl, fipronil, lufenuron and hexaflumuron) at three fixed commercial formulations (500, 1000, and 2000 mg L-1) on the diamondback moth through a leaf dip bioassay.
MATERIALS AND METHODS
An initial P. xylostella colony was collected in August 2008 from cauliflower (Brassica oleracea var. botrytis L.) fields of Shahre-Rey in the south of Tehran, Iran. For the egg-laying, about 500 adults of the P. xylostella were placed in a plastic cage (50 × 30 × 30 cm) and eggs were transferred to cauliflower leaves as food material to continue their development. The insect stock was maintained at 25 ± 1 °C and 65 ± 5% relative humidity under a 16:8 (L:D) photoperiod in a growth chamber.
The commercially formulated insecticides used in the present study were spinosad [Tracer 240 SC (AI), DowAgrosciences, Indianapolis, USA] indoxacarb (Avaunt, 15% EC and 150 SC [AI], DuPont, Cernay, France), pyridalyl (Sumipolo, 50% EC [AI], Sumitomo Chemical, Shikoku, Japan), fipronil (Agenda, 2.5% EC [AI], Agrochemicals, North West Maharashtra, India), lufenuron (Match 50% EC [AI], Syngenta India Limited, Mumbai, India) and hexaflumuron (Consult, 50% EC [AI], Dow Agrosciences, Indianapolis, USA).
Ovicidal assessment test
A leaf dip method was used for all bioassay experiments (Tabashnik and Cushing, 1987). Cabbage (Brassica oleracea var. botrytis L.) leaf disks containing 10 eggs (< 10 h old) of P. xylostella were dipped in three concentrations (500, 1000 and 2000 mg L-1) of commercial formulations of the aforementioned insecticides, including 0.02% Tween-80 for 30 s. In control group, the leaf disks were dipped in water containing 0.02% Tween-80. The treated leaf disks were dried at room temperature for 2 h. Then, the leaf disks were placed in Petri dishes (8 cm in diameter, 1.5 cm depth). The treated eggs were then checked daily until all larvae hatched or the eggs died. Each treatment had four replicates.
Data obtained were subjected to one-way ANOVA (P < 0.05) after checking for normality. Means were compared by Duncan's Multiple Range Test, admitting significant differences at P < 0.05. SAS software was used for all analyses (SAS Institute, 1997).
Tables 1-3 show the effects on P. xylostella of different insecticides at different doses. At 500 mg L-1, the toxic effects of all insecticides, except pyridalyl, were lower than 50%. The efficacy of pyridalyl and hexaflumuron were 65.12 and 47.5%, respectively, and these insecticides were better than the other insecticides in the lowest applied dose. There was no significant difference between control and fipronil, indoxacarb (both formulations) and lufenorun (P < 0.0001, F = 15.19, df = 7.24) (Table 1). At the median concentration (1000 mg L-1), all insecticides, except indoxacarb (EC), significantly affected the hatchability of diamondback moths. Similar to the last dose, treatment with pyridalyl caused the highest and excellent egg mortality (97.72%) (P < 0.0001, F = 41.39, df = 7.24) (Table 2). Table 3 shows the ovicidal effects at the highest tested dose, 2000 mg L-1 (commercial formulation), of the aforementioned insecticides on eggs of P. xylostella. All eggs were killed by pyridalyl, spinosad and hexaflumuron and the mortality of eggs was enhanced as the concentrations increased. Indoxacarb (SC) and fipronil also had a high ovicidal effect on the reduction of egg hatching. Indoxacarb (EC) at 2000 mg L-1 had no significant ovicidal effect compared to the control group (P < 0.0001, F = 12.07, df = 7.24) (Table 3).
The insecticides applied in the present study were effective on eggs of the diamondback moth. Since all tests were performed using the leaf dip method, the ovicidal effect indicated a contact toxicity of these insecticides. To the best of our knowledge, there are few studies regarding the effect of insecticides on eggs of lepidopteran pests and most reports have been focused on the control of larval stage, therefore, little information is available about the effect of pesticide residues on eggs of P. xylostella. Here we showed that pyridalyl has best contact toxicity on eggs of P. xylostella compared to the other tested insecticides (at the median dose). One possible explanation for this could be the high active ingredient (ai) of the aforementioned insecticides. The fipronil and hexaflumuron applied in this study contained 10 and 2.5% ai. Compared to other insecticides, they are more economical for controlling P. xylostella eggs. Concentrations applied for ovicidal effect are higher than those for the larvicidal bioassay. This fact was recorded by Liu et al. (2002). They reported that in the indoxacarb bioassay of Trichoplusia ni (Hubner) (Lep.: Noctuidae), the 50% lethal dose (LC50) for the egg stage is higher than that for the larval stage.
In this study we also observed that spinosad had high toxicity on Lepidoptera eggs. This is supported by Boiteau and Noronha (2007), who treated the European corn borer, Ostrinia nubilalis (Lepidoptera: Crambidae) with spinosad. In the present study, although lufenuron had an ovicidal effect on P. xylostella, it was not as good as the effect of hexaflumuron, another IGR. This could be due to difference in their respective compounds. This is the first study to test the ovicidal effects of hexaflumuron on P. xylostella and the result is almost conclusive. Sáenz-de-Cabezón et al. (2006) showed that lufenuron has ovicidal activity on Lobesia botrana (Lepidoptera: Tortricidae) in contact treatment. El-Barkey et al. (2009) stated that hexaflumuron had ovicidal effects on Pectinophora gossypiella (Saunders) (Lepidoptera: Gelechiidae), an important lepidopteran pest of cotton. Oouchi (2005) reported that an IGR, pyriproxyfen at 100 mg L-1 (AI) caused egg mortality of P. xylostella up to 89%. Here, pyridalyl showed a good ovicidal effect on P. xylostella. Isayama et al. (2005) reported that the efficacy of pyridalyl at 100 mg mL-1 on eggs of Orius stringicollis (Hemiptera: Anthocoridae) was lower than 20%. Vastrad et al. (2005) also estimated the ovicidal action of fipronil and lufenuron on P. xylostella. They observed that lufenuron and fipronil exert ovicidal effects on the diamondback moth. A notable aspect of this study was the strong difference between two formulations of indoxacarb (SC and EC).
The EC formulation in the 500 mg L-1 treatment was similar to the SC formulation, but the 1000 and 2000 mg L-1 groups had lower toxicity on eggs than SC with the same level of active ingredient. Liu et al. (2002) reported that indoxacarb does not have significant ovicidal effect on P. xylostella.
The results of this study indicated that the insecticides applied, except indoxacarb (EC), had good toxicity on the egg stage of the diamondback moth. Among the other insecticides examined, fipronil, spinosad, and hexaflumuron had the greatest efficacy on diamondback moth eggs in response to their active ingredient.
We thank the Department of Agricultural Entomology Research of the Iranian Research Institute of Plant Protection, Tehran, Iran, and the Entomology section of the Department of Plant Protection of Shahed University, Tehran, Iran.
Boiteau, G., and C. Noronha. 2007. Topical, residual and ovicidal contact toxicity of three reduced-risk insecticides against the European corn borer, Ostrinia nubilalis (Lepidoptera: Crambidae), on potato. Pest Management Science 63:1230-1238. [ Links ]
Cole, L.M., R.A. Nicholson, and J.E. Casida. 1993. Action of phenylpyrazole insecticides at the GABA-gated chloride channel. Pesticide Biochemistry and Physiology 46:47-54. [ Links ]
Crouse, G.D., T.C. Sparkts, J. Schoonver, J. Gifford, J. Drippd, T. Bruce, et al. 2001. Recent advances in the chemistry of spinosyns. Pest Management Science 57:177-185. [ Links ]
Dhadialla, T.S., G.R. Carlson, and D.P. Le. 1998. New insecticides with ecdysteroidal and juvenile hormone activity. Annual Review of Entomology 43:545-569. [ Links ]
Dinter, A., and J.A. Wiles. 2000. Safety of the new DuPont insecticide indoxacarb to beneficial arthropods: an overview. IOBC/WPRS Bulletin 23:149-156. [ Links ]
El-Barkey, N.M., A.E. Amer, and M.A. Kandeel. 2009. Ovicidal activity and biological effects of radiant and hexaflumuron against eggs of pink bollworm, Pectinophora gossypiella (Saunders) (Lepidoptera: Gelechiidae). Egyptian Academic Journal of Biological Sciences 2:23-36. [ Links ]
Hoffmann, K.H., and M.W. Lorenz. 1998. Recent advances in hormones in insect pest control. Phytoparasitica 26:1-8. [ Links ]
Isayama, S., S. Saito, K. Kuroda, K. Umeda, and K. Kasamatsu. 2005. Pyridalyl, a novel insecticide: potency and insecticidal selectivity. Archives of Insect Biochemistry and Physiology 58:226-233. [ Links ]
Liu, T., A.N. Sparks, J.R., W. Chen, G.M. Liang, and C. Brister. 2002. Toxicity, persistence, and efficacy of indoxacarb on cabbage looper (Lepidoptera: Noctuidae) on cabbage. Journal of Economic Entomology 95:360-367. [ Links ]
Mahmoudvand, M., A. Sheikhi Garjan, and H. Abbasipour. 2009. Toxicity of neurotoxin insecticides on Diamondback moth, Plutella xylostella (Lep.: Plutellidae). p. 68-69. Proceeding of the 6th Asia-Pacific Congress of Entomology, Entomology in Health, Agriculture and Environment, Beijing, China. 18-22 October 2009. Entomological Society of China, Institute of Zoology, Chinese Academy of Science, China International Conference Center for Science and Technology, Beijing, China. [ Links ]
Meier, G.A., R. Silverman, P.S. Ray, T.G. Cullen, S.F. Ali, F.L. Mared, and C.A. Webster. 1992. Insecticidal dihydropyrazoles with reduced lipophilicity. p. 313-326. In Baker, D R., J.G. Fenyes, and J.J. Steffens (eds.) Synthesis and chemistry of agrochemicals American Chemical Society, Washington DC, USA. [ Links ]
Mertz, P.P., and R.C. Yao. 1990. Saccharopolyspora spinosa sp. nov. isolated from soil collected in a sugar mill rum still. International Journal of Systematic Bacteriology 40:34-39. [ Links ]
Mian, L.S., and M.S. Mulla. 1982. Biological and environmental dynamics of insect growth regulators (IGRs) as used against Diptera of public health importance. Residue Reviews 84:27-112. [ Links ]
Miles, M., and R. Dutton. 2000. Spinosad: a naturally derived insect control agent with potential use in glasshouse integrated pest management systems. Mededelingen Faculteit Landbouwkundige en Toegepaste Biologische Wetenschappen, Universiteit Gent 65:393-400. [ Links ]
Mossan, H.J., J.E. Short, R. Schenker, and J.P. Edwards. 1995. The effects of the insect growth regulator lufenuron on oriental cockroach, Blatta orientalis, and german cockroach, Blattella germanica, populations in simulated domestic environments. Journal of Pesticide Science 45:237-246. [ Links ]
Oouchi, H. 2005. Insecticidal properties of a juvenoid, pyriproxyfen, on all life stages of the diamondback moth, Plutella xylostella (Lepidoptera: Yponomeutidae). Applied Entomology Zoology 40:145-149. [ Links ]
Reynolds, S.E. 1987. The cuticle, growth and moulting in insects: the essential background to the action of acylurea insecticides. Pesticide Science 20:131-146. [ Links ]
Sáenz-de-Cabezón, F.J., E. Martínez-Villar, F. Moreno, V. Marco, and I. Pérez-Moreno. 2006. Influence of sublethal exposure to triflumuron on the biological performance of Tetranychus urticae Koch (Acari: Tetranychidae). Spanish Journal of Agricultural Research 4:167-172. [ Links ]
Saito, S., S. Isayama, Sakamoto, and K. Umeda. 2004. Insecticidal activity of pyridalyl: acute and sub-acute symptoms in Spodoptera litura larvae. Journal Pesticide Science 29:372-375. [ Links ]
Sakamoto, N., S. Saito, T. Hirose, M. Suzuki, S. Matsuo, K.T. Izumi, et al. 2003. The discovery of pyridalyl: a novel insecticidal agent for controlling lepidopterous pests. Pest Management Science 60:25-34. [ Links ]
SAS Institute. 1997. SAS/STAT Guide for personal computers. Version 6.12. SAS Institute, Cary, North Carolina, USA. [ Links ]
Sbragia, R.J., B. Bishabri-Ershadi, R.H. Risterink, D.P. Clilfford, and R. Dutton. 1983. XRD-473, a new acylutea insecticide effective against Heliothis. p. 417-424. Procedings 10th International Congress of Plant Protection, Brighton. 20-25 November. British Crop Protection Council, Croydon, England. [ Links ]
Shelton, A.M., R.J. Cooley, M.K. Kroening, W.T. Wilsey, and S.D. Eigenbrode. 1991. Comparative analysis of two rearing procedures for diamondback moth (Lepidoptera: Plutellidae). Journal of Entomology Science 26:17-26. [ Links ]
Su, N.Y., and J.P. La Fage. 1987. Effects of soldier proportion in the wood consumption rate of the Formosan subterranean termite (Isoptera: Rhinotermitidae). Sociobiology 13:145-151. [ Links ]
Sun, C.N., T.K. Wu, J.S. Chen, and W.T. Lee. 1986. Insecticide resistance in diamondback moth, Management. p. 359-371. In Talekar, N.S., and T.D. Griggs (eds.) Diamondback moth management. Proceedings of the First International Workshop, Asian Vegetable Research and Development Center, Shanhua, Taiwan. 11-15 March 1985. [ Links ]
Tabashnik, B.E., and N.L. Cushing. 1987. Leaf residue vs. topical bioassays for assessing insecticide resistance in the diamondback moth, Plutella xylostella L. FAO Plant Protection Bulletin 35:11-14. [ Links ]
Talekar, N.S., and A.M. Shelton. 1993. Biology, ecology and management of the diamondback moth. Annual Review of Entomology 38:275-301. [ Links ]
Vastrad, A.S., S. Lingappa, and K. Basavangoud. 2005. Ovicides for the management of insecticide resistant populations of diamondback moth, Plutella xylostella (Linnaeus). Journal of Entomological Research 29:49-51. [ Links ]
Wing, K.D., M.E. Schnee, M. Sacher, and M. Connair. 1998. A novel oxadiazine insecticide is bioactivated in lepidopteran larvae. Archives of Insect Biochemistry and Physiology 37:91-103. [ Links ]
Accepted: 30 December 2010.