EVALUATION OF RESIDUAL EFFECTS OF PESTICIDES ON FRUIT FLIES (Drosophila melanogaster)

Authors

  • I. I. Dogara
    Department of Zoology, Faculty of Life Sciences, Federal University of Lafia, PMB 146, Lafia, Nasarawa State, Nigeria.
  • M. A. Ashigar
    Department of Zoology, Faculty of Life Sciences, University of Maiduguri (UNIMAID) P.M.B. 1069, Maiduguri, Borno State, Nigeria.
  • A. Ombugadu
    Department of Zoology, Faculty of Life Sciences, Federal University of Lafia, PMB 146, Lafia, Nasarawa State, Nigeria.
  • J. S. Sangari
    Department of Zoology, Faculty of Life Sciences, Federal University of Lafia, PMB 146, Lafia, Nasarawa State, Nigeria.
  • H. Sani
    Department of Biochemistry, Faculty of Life Sciences, Federal University of Lafia, PMB 146, Lafia, Nasarawa State, Nigeria.
  • J. I. Maikenti
    Department of Zoology, Faculty of Life Sciences, Federal University of Lafia, PMB 146, Lafia, Nasarawa State, Nigeria.
  • H. O. Ahmed
    Department of Zoology, Faculty of Life Sciences, Federal University of Lafia, PMB 146, Lafia, Nasarawa State, Nigeria.
  • V. A. Pam
    Department of Zoology, Faculty of Life Sciences, Federal University of Lafia, PMB 146, Lafia, Nasarawa State, Nigeria.

Keywords:

Fruit fly, Pesticides, Evaluation of residual effects, Non-target organisms

Abstract

Pesticides are used worldwide to control agricultural pests, but their non-target effects on beneficial organisms remain a growing environmental concern. This study evaluates the residual effects of four commonly used pesticides on fruit flies (Drosophila melanogaster) as a model non-target organism. Adult flies were exposed to each pesticide at a 1-10 mmol concentration under controlled conditions, with three replicates per treatment.  Acute toxicity, fecundity eclosion and enzyme activities such as catalase (CAT) and superoxide dismutase (SOD) were measured to assess physiological stress and toxicity using residual film contact method. The results showed that all pesticides induced varying levels of toxicity compared to the untreated control. Lambda-cyhalothrin with the steepest slope (3.45), was most rapid n causing mortality over time with the LC50 value of 4.18 mmol at 72h, 5.23 mmol at 48h and 7.45 mmol at 24h and LC90 of 7.05 mmol at 72h, 8.92 mmol at 48h and 10 mmol at 24h. Glyphosate was the least with LC50 of 5.12 mmol at 72h, 7.83 mmol at 48h and 10 mmol at 24h. Imidacloprid caused the highest reduction in the number eggs laid per female with the mean value of 11.67±4.48 while the least was paraquat (22±5.49). There was no significant difference across the treatment groups (F = 0.825, df = 4, P> 0.539). Imidacloprid was the most toxic against fruit flies eclosion with 100±0.00 % mortality and 0.00 ±0.00% eclosion while paraquat was the least with 81.67±10.93% mortality and 18.67±10.93% eclosion with observed significant difference across the treatment groups (F = 7.554, df = 4, P< 0.005). Glyphosate induced the highest oxidative stress with the SOD and catalase activities of 253.67±82.3 and 215.8±92.9 while the least was lambda-cyhalothrin (742.57±255.6 and 355.4±40.3), respectively. Therefore, there was a significant difference in the SOD activity across the treatment group (F = 39.021, df = 4, P<0.001) likewise catalase activities (F = 7.641, df = 4, P<0.004). These findings indicate that even pesticides intended for specific pests can adversely affect non-target organisms. Therefore, careful selection and use of pesticides are essential to reduced ecological risks and maintain environmental balance.

Dimensions

Bai, D., Lummis, S. C., Leicht, W., Breer, H., & Sattelle, D. B. (1991). Actions of imidacloprid and related nitromethylene on cholinergic receptors of an identified insect motor neurone. Pesticide Science, 33(2),197-204.

Chagnon, M., Kreutzweiser, D., Mitchell, E. A. D., Morrissey, C. A., Noome, D. A., & Van der Sluijs, J. P. (2015). Risks of large-scale use of systemic insecticides to ecosystem functioning and services. Environmental Science and Pollution Research, 22(1), 119–134.

Charpentier, G., Gogo, C., Jactel, H. & Salmo, B. (2014). Sublethal larval exposure to imidacloprid impacts adult behaviour in Drosophila melanogaster. Journal of Evolutionary Biology, 33(2), 151-164.

de Aguiar, L. M., Figueira, F. H., Gottschalk, M. S., & da Rosa, C. E. (2016). Glyphosate-based herbicide exposure causes antioxidant defence responses in the fruit fly Drosophila melanogaster. Comparative Biochemistry and Physiology Part C: Toxicology & Pharmacology, 185(186), 94–101.

Dinis-Oliveira, R. J., Duarte, J. A., Sánchez-Navarro, A., Remião, F., Bastos, M. L., & Carvalho, F. (2008). Paraquat poisonings: Mechanisms of lung toxicity, clinical features, and treatment. Critical Reviews in Toxicology, 38(1), 13–71.

Doaa, A. E. E., Akila, M. E., A. M. Z. M., Amira, A. K. H. N., & Shireen, A. M. (2022). Toxicity and biological effects of certain pesticides and natural oils on the peach fruit fly, Bactrocera zonata (Saunders, 1841) (Diptera: Tephritidae). Polish Journal of Entomology, 91(1), 1–10.

Finney, D. J. (1971). Probit analysis (3rd edition). Cambridge University Press.

Helen, Y.Y., Shane, M. D., Charles, R., & Alexandre, F. (2020). Sublethal larva exposure to imidacloprid impacts adults’ behaviours in Drosophila melanogaster. Journal of Environmental Biology, 33(2), 151-164.

Jennings, B. H. (2011). Drosophila – a versatile model in biology & medicine. Materials Today, 14(5), 190–195.

Jeschke, P., Nauen, R., Schindler, M., & Elbert, A. (2011). Overview of the status and global strategy for neonicotinoids. Journal of Agricultural and Food Chemistry, 59(7), 2897–2908.

Markow, T. A., & O’Grady, P. M. (2006). Drosophila: A guide to species identification and use. Academic Press. 245 pp.

Martelli, F., Zhong, Y., Mackay, T. F. C., & Batterham, P. (2020). Low doses of the neonicotinoid insecticide imidacloprid induce ROS triggering neurological and metabolic impairments in Drosophila. Proceedings of the National Academy of Sciences, 117(41), 25840-25850.

Mota-Sanchez, D., & Wise, J. C. (2022). Insecticide Resistance in Arthropods. In Insect Resistance Management (3rd ed.). Academic Press.

Motta, E. V. S., Raymann, K., & Moran, N. A. (2018). Glyphosate perturbs the gut microbiota of honey bees. Proceedings of the National Academy of Sciences, 115(41), 10305-10310.

Mottaleb, M. A., Lopata, A. L., & Reid, S. (2022). Imidacloprid induces oxidative stress and locomotor deficits in Drosophila melanogaster: A study on time-dependent toxicity and antioxidant response. Ecotoxicology and Environmental Safety, 241, 113811.

National Institute of Standard and Technology (2000). Preparation and calibration of standard solution. NIST Recommendation Guide: Special publication, 9602.

Oliveira, P. F. R., Molon, B. B., Pereira, L. V., Nascimento, L. T., Marques, V. A. C. M., Vilela, L. C., Silva, R. B., Schmidt, J. H., Kessler, G. P., Ritzel, E. C., Sanz, E. L. S., Vieira, M. Q., Bogo, P. B., Macedo, R. G., Wyse, A., & Xavier, L. L. (2022). Age-related tolerance to paraquat-induced parkinsonism in Drosophila melanogaster. Toxicology Letters, 361, 43–53.

Pal, S., Chizukonda, R. T., & Singh, M. P. (2019). Drosophila melanogaster as a model for studying the neurotoxicity of paraquat: A review. Neurotoxicology, 72, 154-163.

Pandey, U. B. & Nichols, C. D. (2011). Human disease models in Drosophila melanogaster and the role of the fly in therapeutic drug discovery. Pharmacological Reviews, 63(2), 411–436.

Pisa, L. W., Amaral-Rogers, V., Belzunces, L. P., Bonmatin, J. M., Downs, C. A., Goulson, D., Kreutzweiser, D. P., Krupke, C., Liess, M., McField, M., Morrissey, C. A., Noome, D. A., Settele, J., Simon-Delso, N., Stark, J. D., Van der Sluijs, J. P., Van Dyck, H., & Wiemers, M. (2015). Effects of neonicotinoids and fipronil on non-target invertebrates. Environmental Science and Pollution Research, 22(1), 68-102.

Plapp, F. W. Bigley, W. S., Chapmen, G. A., & Eddy, G. W. (1963). Synergism of malathion against resistant house flies and mosquitoes. Journal of Economic Entomology, 56, 643-649

Rand, G. M. (Ed.). (1995). Fundamentals of Aquatic Toxicology: Effects, Environmental Fate, and Risk Assessment (2nd ed.). Taylor & Francis.

Ruan, Z., & Zhang, Y. (2022). Paraquat-induced oxidative stress delays metamorphosis and reduces eclosion success in Drosophila melanogaster. Ecotoxicology, 31(4), 679–689.

Sang, J. H., & Reeve, E. C. (2001). Drosophila melanogaster: The fruit fly. Encyclopedia of genetics. USA: Fitzroy Dearborn publisher, p. 157.

Sharma, A., Kumar, V., Shahzad, B., Tanveer, M., Sidhu, G. P. S., Handa, N., Kohli, S. K., Yadav, P., Bali, A. S., Parihar, R. D., Dar, O. I., Singh, K., Jasrotia, S., Bakshi, P., Ramakrishnan, M., Kumar, S., Bhardwaj, R., & Thukral, A. K. (2019). Worldwide pesticide usage and its impacts on ecosystem. SN Applied Sciences, 1(11), 1446.

Silva, J. J., Silva, W. J, Guedes, R. N. C., & DA Silva, C. B. (2013). Effect of sublethal doses of the insecticide imidacloprid on adaptive traits of Drosophila melanogaster: Response to treatment over and after 15 consecutive generations. Open Journal of Animal Sciences, 3(4B), 8-19.

Smith, A. M., Moret, R., & Douglas, A. E. (2021). Glyphosate-based herbicide exposure alters antioxidant defense and redox status in Drosophila melanogaster. Chemosphere, 262, 127827.

Soderlund, D. M. (2012). Molecular mechanisms of pyrethroid insecticide neurotoxicity: Recent advances. Archives of Toxicology, 86(2), 165–181.

Tosi, S., Sfeir, C., Carnesecchi, E., van Engelsdorp, D., & Chauzat, M. P. (2022). Lethal, sublethal, and combined effects of pesticides on bees: A meta-analysis and new risk assessment tools. Science of The Total Environment, 844, 156857.

Van Bruggen, A. H. C., He, M. M., Shin, K., Mai, V., Jeong, K. C., Finckh, M. R., & Morris, J. G., Jr. (2018). Environmental and health effects of the herbicide glyphosate. Science of The Total Environment, 616(617), 255–268.

Published

2026-10-31

How to Cite

EVALUATION OF RESIDUAL EFFECTS OF PESTICIDES ON FRUIT FLIES (Drosophila melanogaster). (2026). THE INCUBATOR: Journal of Postgraduate Studies, FULafia, 1(1), 30. https://journals.fulafia.org.ng/index.php/incubator/article/view/30

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STEM SECTION

How to Cite

EVALUATION OF RESIDUAL EFFECTS OF PESTICIDES ON FRUIT FLIES (Drosophila melanogaster). (2026). THE INCUBATOR: Journal of Postgraduate Studies, FULafia, 1(1), 30. https://journals.fulafia.org.ng/index.php/incubator/article/view/30

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