Evaluation of Toxicity of Some New Insecticides against Egg Parasitoid Trichogramma chilonis (Ishii) (Hymenoptera: Trichogrammitidae)

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Pakistan J. Zool., vol. 44(4), pp. 1123-1127, 2012. Evaluation of Toxicity of Some New Insecticides against Egg Parasitoid Trichogramma chilonis (Ishii) (Hymenoptera: Trichogrammitidae) Dilbar Hussain 1*, Amjad Ali 1, Muhammad Mushtaq-ul-Hassan 2, Saira Ali 2, Muhammad Saleem 1 and Sajid Nadeem 3 1 Entomological Research Institute, Ayub Agricultural Research Institute, Faisalabad. 2 Department of Zoology, GC University, Faisalabad. 3 Nuclear Institute for Agriculture and Biology, Faisalabad. Abstract.- Toxicity of some new insecticides viz., spinosad, lufenuron, flubendiamide, chlorantraniliprole, emamectin benzoate and imidacloprid were tested against immature and adult stages of Trichogramma chilonis (Ishii) (Hymenoptera: Trichogrammitidae) under laboratory conditions. Exposure of spinosad to T. chilonis resulted in the lowest emergence at all the parasitism situations. The application of emamectin benzoate and lufenuron after 1 st day parasitism, imidacloprid, emamectin benzoate and lufenuron after 3 rd day parasitism, imidacloprid, emamectin benzoate, flubendiamide and lufenuron after 4, 5 and 7 days of parasitism, respectively showed minimum effect on the emergence of T. chilonis and were found to be safe to the parasitoid. After 8-days parasitism, chlorantraniliprole resulted in maximum emergence of T. chilonis and did not show significant difference with lufenuron and emamectin benzoate. Chlorantraniliprole showed maximum survival (42%) and did not differ significantly with lufenuron with 36% survival at 3 h post application. Emamectin benzoate was found to be a toxic insecticide which resulted in minimum survival of the parasitoid with 18.0% and did not show significant differences to those of imidacloprid with 22.0% survival. All the insecticides showed non-significant difference with one another on the survival of T. chilonis adults recorded 24 h post application and found toxic to the adults of T. chilonis regarding survival range between 8.0 to 14.0% as against control treatment with 92.0% survival of T. chilonis adult. Key words: Trichogramma chilonis, egg parasitoid, spinosad, lufenuron, flubendiamide, chlorantrasiliprole, emamectin benzoate, imidacloprid. INTRODUCTION The use of Trichogramma species in many crop ecosystems has achieved appreciable pest control success and its role in the biological control programs of pest management is well understood (Smith, 1996; Sorokina, 1999; Hussain et al., 2010). By the establishment of Bio-intensive Pest Management Programs (BIPM), bio-control agents, such as Trichogramma species are integrated with other control methods without affecting the efficiency of bio-control agents (Tiwari and Khan, 2004) and is most widely used in Pakistan, India, China, Korea, Taiwan, Japan, Nepal, and Reunion Island and as exotic species in Kenya, Spain, South Africa and Australia. Trichogramma can survive into a wide range of temperature and gave successful control of lepidopteran pests in many crops (Nadeem and Hamed, 2008; Nadeem et al., * Corresponding author: roy_dilbar@yahoo.com 0030-9923/2012/0004-1123 $ 8.00/0 Copyright 2012 Zoological Society of Pakistan. 2009, 2010; Nadeem and Hamed, 2011). Application of selective insecticides to control pests could be useful in conservation of natural enemies associated with crops. The insecticides that are widely used to control different pests can affect the effectiveness of these beneficial agents. It is not fully clear, to what extent insecticides are harmful for other non-target organisms. More understanding of pest natural enemy insecticide interaction is needed to formulate more effective integrated pest management strategies (Preetha et al., 2010). Some new insecticides are potentially more toxic to the target pest but not to natural enemies, thus playing significant role in conservation of biological control agents in agricultural environments. In some pest management systems, pesticides that have been used as selective shown harmful effects on beneficial species (Hill and Foster, 2000). Work of the previous researchers like Charles et al. (2000), Ughade et al. (2002), Preetha et al. (2009) and Sattar et al. (2011) indicated toxic effects of different insecticides on Trichogramma

1124 D. HUSSAIN ET AL. spp. Williams and Price (2004) tested the toxic effects of spinosad, thiamethoxam and oxamyl) on egg parasitoid, T. pretiosum, with order of toxicity was thiamethoxam > spinosad > oxamyl (Vianna et al., 2009) found that lufenuron had lowest negative effects on parasitism and viability of individuals of T. pretiosum populations. Hussain et al. (2010) revealed that emamectin benzoate, lufenuron, and imidacloprid had a significant adverse effect on the emergence of T. chilonis when exposed to all immature stages of development inside the host eggs of Sitotroga cerealella by exposure to imidacloprid, emamectin benzoate and lufenuron with 70.02, 27.62, and 18.48% survival, respectively, after 3 h but after 24 h none of the insecticides was found safe to T. chilonis adult. Preetha et al. (2010) found that imidacloprid 7.8 SL did not cause any adverse effect on the adult emergence and parasitism of T. chilonis. Numerous laboratory and field studies have revealed that Trichogramma wasps are highly susceptible to most broad spectrum insecticides. This is the reason that various attempts to suppress pest population by biological control measures have often failed because of deleterious effects of chemical on the beneficial insects (Borgemeister et al., 1993). The integration of biological and chemical control tactics requires a thorough understanding of effects on biological control agents. A step-wise assessment, moving from the laboratory to the field, with proper consideration of both direct and sublethal effects is recommended in the screening of pesticides against biological control agents (Croft, 1990). The present investigation was undertaken to study the selective toxicity of different new insecticides against T. chilonis under laboratory conditions with an objective to search for comparatively less toxic insecticide against T. chilonis, to be incorporated into IPM programs. MATERIALS AND METHODS Six insecticides were tested against T. chilonis at adult and immature stages in the Insect Rearing Laboratory of Entomological Research Institute, Ayub Agricultural Research Institute, Faisalabad. The experiment was laid out in completely randomized design with five repeats. The control treatment was also maintained where only tap water was sprinkled. Some new insecticides which are being commonly used to control insect pests of many crops in the field were selected (Table I). Each insecticide was measured with micro pipette and was kept in a beaker to make the volume 500 ml with distilled water, shaken to ensure the thorough mixing. The following bio-assays were done. Egg card bioassay The effect of dipping parasitized (T. chilonis on host eggs) S. cerealella in different insecticides were studied during different immature stages of T. chilonis. Five randomly selected egg cards, each having 40 parasitoid eggs were dipped into each treatment for one second on 1 st, 3 rd, 4 th, 5 th, 7 th and 8 th day of age of parasitoid eggs. These days corresponded to the developmental stages of Trichogramma: eggs 1d, larvae 3d, pre-pupae 4d, early pupae 5d, pupae 7d, and late pupae or one day before adult emergence 8d. Dipped egg cards were dried at ambient room temperature. Once dried, each egg card was placed in a small glass petri dish (5 cm diameter and 0.5cm deep) held at 27±1 C and relative humidity 65±5% until all healthy parasitoids had emerged. The eggs were then observed under microscope for their emergence. Dipped surface residue bioassay The effect of insecticide residues on the survival of adult of T. chilonis was studied in ventilated glass bio-assays chambers measuring 15x4 cm (Scholz, 1994). Whatman filter paper was saturated in a solution of each treatment then dried and were kept into the glass bio-assays tube to fully exposed the treatment. Approximately ten newly emerged T. chilonis adults were released in each bio-assay tube and exposed to the treated filter paper for 3 h and 24 h. After exposure, the number of dead and alive wasps was recorded. Each of the treatment was replicated 5 times. Statistical analysis The data were subjected to analysis of variance (ANOVA) followed by means separation using Fisher s least significant difference (LSD) test at 5% (Steel et al., 1997).

SELECTIVE TOXICITY OF NEW INSECTICIDES AGAINST EGG PARASITOID 1125 Table I.- Insecticides tested against T. chilonis. Name of insecticides Trade name Dose rate ml/ha Manufacturer/Distributor Spinosad 240 SC Tracer 198 Dow Agro Sciences/ Arysta Life Science Pakistan Lufenuron 50 EC Match 494 Syngenta, Pakistan Flubendiamide 480 SC Belt 432 Bayer Crop Sciences Chlorantraniliprole 20 SC Coragen 72 DuPont Pakistan/ UDL, Pakistan Emamectin benzoate 1.9 EC Proclaim 494 Syngenta, Pakistan Imidacloprid 200 SL Confidor 618 Bayer Crop Sciences RESULTS AND DISCUSSION Table II shows that the exposure of spinosad to parasitoids, T. chilonis, resulted in the lowest emergence (4.6% to 26.8%), while the highest emergence (17.8% to 70.5%) was observed after exposure to Chlorantraniliprole. The present results agree to the findings of Ughade et al. (2002) who reported that spinosad was moderately safer to T. chilonis. The order of toxicity was thiamethoxam > spinosad >oxamyl as reported by Williams et al. (2004) also did not agree to our findings. Emergence of parasitoids after application of emamectin benzoate (67.5%) and lufenuron (64.0%) after 1 st day parasitoids, imidacloprid (62.5%), emamectin benzoate (68.5%) and lufenuron (65.0%) after 2 nd day parasitoids, imidacloprid (63.9, 65.0 and 65.0%), emamectin benzoate (70.5, 68.8 and 68.9%), flubendiamide (62.4, 64.0 and 62.5%) and lufenuron (66.0, 67.5 and 66.0% after 4, 5 and 7 days parasitism, respectively) showed minimum effect on the emergence of T. chilonis and was found safer to the parasitoid eggs. Emamectin benzoate, lufenuron, flubendiamide and imidacloprid were observed to be safer compared to chlorantraniliprole against Trichogramma. The present findings are in conformity to those of Ughade et al. (2002) who reported that imidacloprid was moderately safe towards the emergence of T. chilonis. Our findings did not agree to those of Nasreen et al. (2004) and Preetha et al. (2009) who found that imidacloprid was toxic to T. chilonis under laboratory conditions. Eight day old parasitoid eggs showed the highest emergence of T. chilonis (70%) after exposure to chlorantraniliprole which did not differ significantly from lufenuron (66.5%) and emamectin benzoate (69.5%). According to Vianna et al. (2009), lufenuron had lowest adverse effects on parasitism and viability of Trichogramma species. The present findings are consistent with those of Preetha et al. (2010) who reported that imidacloprid did not cause any adverse effect on the adult emergence and parasitism of T. chilonis. The results reported by Hussain et al. (2010) which showed that lufenuron, emamectin benzoate and imidacloprid have significant adverse effects on the emergence of T. chilonis are inconsistent to our present findings. In the present experiments, all the insecticides differed significantly regarding survival of adults of T. chilonis 3 h post application (Table III). Chlorantraniliprole resulted in maximum survival i.e., 42% 3 h after application and did not show significant difference from lufenuron which showed 36% survival. Emamectin benzoate was found to be a toxic insecticide resulted in low survival (18.0%) of the adult parasitoids and did not show significant difference from imidacloprid, where 22.0% survival was recorded. All the insecticides showed nonsignificant differences to each other on the survival of T. chilonis adults 24 h post application and were found toxic to the adults of T. chilonis where survival ranged between 8.0 to 14% compared to 92.0% in control. From these results, it is clear that chlorantraniliprole had less knockdown effect as compared to other insecticides and at 24 h post treatment, all the insecticides were equally toxic to the parasitoid at adult stage. The present findings agreed to the work of Preetha et al. (2009) who reported that Imidacloprid was toxic and chlorantraniliprole was harmless to T. chilonis. Vianna et al. (2009) also reported that lufenuron had lowest negative effects on parasitism and viability of individuals of T. pretiosum populations. Our findings are consistent to those of Hussain et al.

1126 D. HUSSAIN ET AL. Table II.- Adult emergence (%) of T. chilonis at different post treatment intervals of insecticides. Insecticides 1 st Day 3 rd Day 4 th Day 5 th Day 7 th Day 8 th Day Spinosad 16.2 d 26.8 d 4.6 d 25.6 d 21.0 d 24.0 d Lufenuron 64.0 bc 65.0 b 66.0 b 67.5 b 66.0 b 66.5 bc Flubendiamide 61.1 c 61.5 b 62.4 b 64.0 b 62.5 b 63.5 c Chlorantraniliprole 17.8 d 37.4 c 31.8 c 44.2 c 38.8 c 70.0 b Emamectin benzoate 67.5 b 68.5 b 70.5 b 68.8 b 68.9 b 69.5 bc Imidacloprid 61.6 c 62.5 b 63.9 b 65.0 b 65.0 b 63.5 c Control 93.5 a 95.0 a 96.5 a 94.4 a 93.4 a 93.0 a LSD at P =5 % 5.38 7.83 11.30 6.48 6.73 6.48 F. Value 226.0 67.00 57.79 92.65 99.65 83.48 C.V. (%) 7.62 10.16 15.43 8.15 8.75 7.79 Means sharing similar alphabets are not significantly different to each other. Table III.- Insecticide Survival (%) of T. chilonis adults at different post treatment intervals of insecticides. Survival (%) After 3 h After 24 h Spinosad 28.0 cd 10.0 b Lufenuron 36.0 bc 14.0 b Flubendiamide 32.0 c 14.0 b Chlorantraniliprole 42.0 b 8.0 b Emamectin benzoate 18.0 e 8.0 b Imidacloprid 22.0 de 12.0 b Control 94.0 a 92.00 a LSD at P =5 % 9.29 9.05 F. Value 63.88 97.13 C.V. (%) 18.46 30.88 Means sharing similar alphabets in a column are not significantly different to each other. (2010) who reported that at adult Trichogramma exposure to imidacloprid, emamectin benzoate and lufenuron had 70.0, 27.6, and 18.4% survival, respectively after 3 h, but for 24 h, none of the insecticides was found to be safe to adult of T. chilonis. The conclusion drawn from above results showed that spinosad was found to be very toxic based on the emergence of T. chilonis followed by chlorantraniliprole. Rest of the tested insecticides were found toxic based on the survival of adult parasitoids. REFERENCES BORGEMEISTER, C., POEHLING, H.M., DINTER, A. AND HOLLER, C., 1993. Effects of insecticides on life history parameters of the aphid parasitoid Aphidius rhopalosiphi (Hymn.: Aphidiidae). Emtomophaga, 38: 245-255. CHARLES, P.C.S., DAVID, B.O. AND JOHN, W.V.D., 2000. Effect of insecticides on Trichogramma exiguum (Trichogrammatidae: Hymenoptera) pre-imaginal development and adult survival. J. econ. Ent., 93: 577-583. CROFT, B.A., 1990. Arthropod biological control agents and pesticides. Wiley, New York. Crops. CAB International. HILL, T. A. AND FOSTER, R.E., 2000. Effect of insecticides on the diamondback moth (Lepidoptera: Plutellidae) and its parasitoid Diadegma insulare (Hymenoptera: Ichneumonidae). J. econ. Ent., 93: 763-768. HUSSAIN, D., AKRAM, M., IQBAL, Z., ALI, A. AND SALEEM, M., 2010. Effect of insecticides on Trichogramma chilonis Ishii. (Hymenoptera: Trichogrammatidae) immature and adult survival. J. agric. Res., 48: 531-537. NADEEM, S. AND HAMED, M., 2008. Comparative development and parasitization of Trichogramma chilonis Ishii and Trichogrammatoidea bactrae Nagaraja under different temperature conditions. Pakistan J. Zool., 40: 431-434. NADEEM, S. AND HAMED, M., 2011. Biological control of sugarcane borers with inundative releases of Trichogramma chilonis (Ishii) (Hymenoptera: Trichogrammatidae) in farmer fields. Pakistan J. agric. Sci., 48: 71-74. NADEEM, S., ASHFAQ, M., HAMED, M. AND AHMED, S., 2010. Optimization of short and long term storage duration for Trichogramma chilonis (Ishii) (Hymenoptera: Trichogrammatidae) at low temperatures. Pakistan J. Zool., 42: 63-67. NADEEM, S., ASHFAQ, M., HAMED, M., AHMED, S. AND NADEEM, M.K., 2009. Comparative rearing of Trichogramma chilonis at different temperatures conditions. Pak. Ent., 31: 33-36. NASREEN, A., CHEEMA, G.M., ASHFAQ, M. AND

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