Sublethal doses of Eucalyptus benthamii essential oil induce overcompensatory responses in Aedes aegypti (Diptera: Culicidae)
DOI:
https://doi.org/10.5327/Z2176-94782882Keywords:
larval density; insecticide; natural compounds; vector controlAbstract
Managing mosquito populations remains the most effective approach to mitigating arbovirus transmission. However, stressor-induced mortality under determined conditions can trigger compensatory or overcompensatory effects in adult mosquito characteristics (total biomass, individual size). In this study, we evaluated the role of Eucalyptus benthamii essential oil as a stressor on Aedes aegyptilarvae, investigating its effects on larval development, adult size, longevity, and overall adult emergence. First-instar A. aegypti larvae were subjected to essential oil concentrations of 8.5 (LD50) and 18.5 ppm (LD90) in controlled laboratory conditions. We assessed pupal mortality, the proportion of pupae that successfully transitioned to adulthood, adult longevity (in days), larval growth rates, wing length, and overall larval mortality. The results revealed that the interaction between time and treatment had a significant effect on larval mortality. Although the essential oil concentration did not affect the number of larvae reaching adulthood, adult longevity and larval development time were notably extended under LD90 and LD50 concentration, respectively. Larval mortality rates were highest during the first week of exposure to the LD90 treatment. Furthermore, males and females produced in microcosms with LD50 and LD90 had significantly larger wings than in the control. These findings suggest that sublethal doses of E. benthamii essential oil may enhance certain adult A. aegypti population characteristics through overcompensatory mortality.
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Abrams, P. A., 2009. When does greater mortality increase population size? The long history and diverse mechanisms underlying the hydra effect. Ecology Letters, v. 12, (5), 462-474. https://doi.org/10.1111/j.1461-0248.2009.01282.x.
Abrams, P. A.; Matsuda, H., 2005. The effect of adaptive change in the prey on the dynamics of an exploited predator population. Canadian Journal of Fisheries and Aquatic Sciences, v. 62, (4), 758-766. https://doi.org/10.1139/f05-051.
Aldridge, R. L.; Alto, B. W.; Connelly, C. R.; Okech, B.; Siegfried, B.; Eastmond, B. H.; Alomar, A. A.; Linthicum, K. J., 2024. Does prior exposure to larvicides influence dengue virus susceptibility in Aedes aegypti (Diptera: Culicidae)? Journal of Medical Entomology, v. 61, (1), 166-174. https://doi.org/10.1093/jme/tjad137.
Alto, B. W.; Lord, C. C., 2016. Transstadial effects of Bti on traits of Aedes aegypti and infection with dengue virus. PLoS Neglected Tropical Diseases, v. 10, (2), e0004370. https://doi.org/10.1371/journal.pntd.0004370.
Amaral, W. D.; Deschamps, C.; Bizzo, H. R.; Pinto, M. A. S.; Biasi, L. A.; Silva, L. E. 2017. Essential oil yield and composition of native tree species from Atlantic forest, south of Brazil. Journal of Essential Oil Bearing Plants, v. 20, (6), 1525-1535. https://doi.org/10.1080/0972060X.2017.1346484.
Bellamy, S. K.; Paige, A.; Alto, B. W., 2024. Trait- and density-mediated effects of predation on fecundity and fertility of Aedes aegypti (Diptera: Culicidae) mosquitoes. Journal of Medical Entomology, v. 61, (1), 132-141. https://doi.org/10.1093/jme/tjad146.
Beserra, E. B.; Fernandes, C. R. M.; Ribeiro, P. S., 2009. Relação entre densidade larval e ciclo de vida, tamanho e fecundidade de Aedes (Stegomya) aegypti (L.) (Diptera: Culidade) em laboratório. Neotropical Entomology, v. 38, 847-852. https://doi.org/10.1590/S1519-566X2009000600020.
Borges, W. G.; Cozzer, G. D.; Durigon, G. R.; Lima-Rezende, C. A.; Rezende, R. S., 2023. Predator presence influences life history traits of Aedes aegypti. Aquatic Sciences, 85, (2), 58. https://doi.org/10.1007/s00027-023-00952-0.
Carvalho, G.; Cozzer, G. D.; Almeida, M. O. P.; Borges, W. G.; Rezende, R. S.; Godoy, B. S.; Silva, I. M.; Oliveira, J. V.; Albeny-Simões, D.; Dal Magro, J., 2025. Assessing neighbourhood-scale BTI spray applications and laboratory-based mortality testing on Aedes aegypti larval development. Bulletin of Entomological Research, v. 115, (1), 56-65. https://doi.org/10.1017/S0007485324000889.
Chellappandian, M.; Vasantha-Srinivasan, P.; Senthil-Nathan, S.; Karthy, S.; Thanigaivel, A.; Ponsankar, A.; Kalaivani, K.; Hunter, W. B., 2018. Botanical essential oils and uses as mosquitocides and repellents against dengue. Environment International, v. 113, 214-230. https://doi.org/10.1016/j.envint.2017.12.038.
Collins, E. L.; Quintana, J. M.; Morales, R.; Moss, S.; Acford-Palmer, H.; Higgins. M.; Phelan. J.; Clark, T. G.; Brown, G.; Campino, S., 2025. Profiling insecticide resistance phenotypes and genotypes in Aedes aegypti populations across four regions in Puerto Rico. Scientific Reports, v. 15, 26116. https://doi.org/10.1038/s41598-025-03709-x.
Cozzer, G. D.; Ilha, C.; Borges, W. G.; Lima-Rezende, C. A.; Dal Magro, J.; Souza Rezende, R., 2025. The role of larval density and food availability in life-history traits of Aedes aegypti mosquitoes. Entomologia Experimentalis et Applicata, v. 173, (8), 892-902. https://doi.org/10.1111/eea.13585.
Cozzer, G. D.; Lara, T. S.; Dal Magro, J.; Albeny-Simões, D.; Rezende, R. S., 2024. How much is needed to survive? Minimal nutritional levels to complete the development on Aedes aegypti (Diptera: Culicidae). Limnetica, v. 43, (2), 239-251. https://doi.org/10.23818/limn.43.16.
Cozzer, G. D.; Rezende, R. S.; Lara, T. S.; Machado, G. H.; Dal Magro, J.; Albeny-Simões, D., 2023. Predation risk effects on larval development and adult life of Aedes aegypti mosquito. Bulletin of Entomological Research, v. 113, (1), 29-36. https://doi.org/10.1017/S000748532200027X.
Crawley, M. J., 2007. The R Book. John Wiley & Sons Inc., Chichester, 951 p. https://doi.org/10.1002/9780470515075.
Demarque, D. P.; Espindola, L. S., 2021. Challenges, advances and opportunities in exploring natural products to control arboviral disease vectors. Frontiers in Chemistry, v. 9, 779049. https://doi.org/10.3389/fchem.2021.779049.
França, L. P.; Amaral, A. C. F.; Ramos, A. S.; Ferreira, J. L. P.; Maria, A. C. B.; Oliveira, K. M. T.; Araujo Jr., E. S.; Branches, A. D. S.; Silva, J. N.; Silva, N. G.; Barros, G. A.; Chaves, F. C. M.; Tadei, W. P.; Silva, J. R. A., 2021. Piper capitarianum essential oil: a promising insecticidal agent for the management of Aedes aegypti and Aedes albopictus. Environmental Science and Pollution Research, v. 28, (8), 9760-9776. https://doi.org/10.1007/s11356-020-11148-6.
Gallon, C.; Martello, R. H.; Cozzer, G. D.; Lima-Rezende, C. A.; Calisto, J. F. F.; Floss, P. A.; Oliveira, J. V.; Rezende, R. S.; Dal Magro, J.; Albeny-Simões, D. 2020. Chemistry matters: biological activity of Eucalyptus essential oils on mosquito larval mortality. Entomologia Experimentalis et Applicata, v. 168, (5), 407-415. https://doi.org/10.1111/eea.12908.
Gutiérrez, E. H. J.; Riehle, M. A.; Walker, K. R.; Ernst, K. C.; Davidowitz, G., 2022. Using body size as an indicator for age structure in field populations of Aedes aegypti (Diptera: Culicidae). Parasites Vectors, v. 15, 483. https://doi.org/10.1186/s13071-022-05605-z.
Hall, D. R.; Johnson, R. M.; Kwon, H.; Ferdous, Z.; Laredo-Tiscareño, S. V.; Blitvich, B. J.; Brackney, D. E.; Smith, R. C., 2025. Mosquito immune cells enhance dengue and Zika virus infection in Aedes aegypti. Nature Communications, v. 16, 5891. https://doi.org/10.1038/s41467-025-61139-9.
Hastings, A., 2013. Population dynamics. In: Levin, S. A. (Eds.), Encyclopedia of Biodiversity: Second Edition. Elsevier, Amsterdam, pp. 175-181. https://doi.org/10.1016/B978-0-12-384719-5.00115-5.
Keumeni, C. R.; Yougang, A. P.; Njiokou, F.; Clarke, S. E.; Wondji, C.; Kamgang, B., 2025. Association of knockdown resistance mutations with pyrethroid resistance in Aedes aegypti, a major arbovirus vector in Cameroon. Parasites Vectors, v. 18, 296. https://doi.org/10.1186/s13071-025-06943-4.
Marques, D. M.; Rocha, J. F.; Almeida, T. S.; Mota, E. F., 2021. Essential oils of caatinga plants with deletary action for Aedes Aegypti: a review. South African Journal of Botany, v. 143, 69-78. https://doi.org/10.1016/j.sajb.2021.08.004.
Marsaro, I. B.; Cozzer, G. D.; Cararo, E. R.; de Brito, R.; Borges, W. G.; Dal Magro, J.; Lima-Rezende, C. A.; Rezende, R. S., 2023. Less is more: partial larvicidal efficacy of plant leachate leads to larger mosquitoes. Bulletin of Entomological Research, v. 113, (5), 684-692. https://doi.org/10.1017/S0007485323000366.
Moral, R. A.; Hinde, J.; Demétrio, C. G. B., 2017. Half-normal plots and overdispersed models in R: the hnp package. Journal of Statistical Software, v. 81, (10), 1-23. https://doi.org/10.18637/jss.v081.i10.
Mossi, A. J.; Astolfi, V.; Kubiak, G.; Lerin, L.; Zanella, C.; Toniazzo, G.; Oliveira, D.; Treichel, H.; Devilla, I. A.; Cansian, R.; Restello, R., 2011. Insecticidal and repellency activity of essential oil of Eucalyptus sp. against Sitophilus zeamais Motschulsky (Coleoptera, Curculionidae). Journal of the Science of Food and Agriculture, v. 91, (2), 273-277. https://doi.org/10.1002/jsfa.4181.
Muturi, E. J.; Kim, C. H.; Alto, B. W.; Berenbaum, M. R.; Schuler, M. A., 2011. Larval environmental stress alters Aedes aegypti competence for Sindbis virus. Tropical Medicine and International Health, v. 16, (8), 955-964. https://doi.org/10.1111/j.1365-3156.2011.02796.x.
Powell, J. R.; Gloria-Soria, A.; Kotsakiozi, P., 2018. Recent history of Aedes aegypti: Vector genomics and epidemiology records. BioScience, v. 68, (11), 854-860. https://doi.org/10.1093/biosci/biy119.
Rattan, R. S., 2010. Mechanism of action of insecticidal secondary metabolites of plant origin. Crop Protection, v. 29, (9), 913-920. https://doi.org/10.1016/j.cropro.2010.05.008.
Schröder, A.; van Leeuwen, A.; Cameron, T. C., 2014. When less is more: Positive population-level effects of mortality. Trends in Ecology and Evolution, v. 29, (11), 614-624. https://doi.org/10.1016/j.tree.2014.08.006.
Silva Ferreira, R.; Toni Aquino da Cruz, L. C.; Souza, V. J.; Silva Neves, N. A.; Souza, V. C.; Franco Filho, L. C.; Silva Lemos, P.; Lima, C. P. S.; Naveca, F. G.; Atanaka, M.; Nunes, M. R. T.; Slhessarenko, R. D., 2020. Insect-specific viruses and arboviruses in adult male culicids from Midwestern Brazil. Infection, Genetics and Evolution, v. 85, 104561. https://doi.org/10.1016/j.meegid.2020.104561.
Vivekanandhan, P.; Usha-Raja-Nanthini, A.; Valli, G.; Subramanian Shivakumar, M., 2020. Comparative efficacy of Eucalyptus globulus (Labill) hydrodistilled essential oil and temephos as mosquito larvicide. Natural Product Research, v. 34, (18), 2626-2629. https://doi.org/10.1080/14786419.2018.1547290.
Walker, M.; Robert, M. A.; Childs, L. M., 2021. The importance of density dependence in juvenile mosquito development and survival: A model-based investigation. Ecological Modelling, v. 440, 109357. https://doi.org/10.1016/j.ecolmodel.2020.109357.
Williams, G. M.; Faraji, A.; Unlu, I.; Healy, S. P.; Farooq, M.; Gaugler, R.; Hamilton, G.; Fonseca, D. M., 2014. Area-wide ground applications of Bacillus thuringiensis var. israelensis for the control of Aedes albopictus in residential neighborhoods: from optimization to operation. PLoS One, v. 9, (10), e110035. https://doi.org/10.1371/journal.pone.0110035.
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Copyright (c) 2026 Carine Gallon, Gilberto Dinis Cozzer, Regiane Chiamente Pessetti, Bruno Spacek Godoy, Cassiano Sousa Rosa, Ivoneide Maria da Silva, Renan de Souza Rezende, José Vladmir Oliveira, Jacir Dal Magro, Daniel Albeny-Simões

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