Biological parameters and age–stage, two–sex life table of the parasitoid wasp Encarsia formosa feeding on nymphs of the greenhouse whitefly Trialeurodes vaporariorum on three important greenhouse crops

Document Type : Research Paper

Authors

1 Assistant Professor, Agricultural Research, Education and Extension Organization (AREEO), Agricultural and Natural Resources Research and Education Center of Isfahan, Plant Protection Research Department, Isfahan, Iran.

2 Professor, University of Mohaghegh Ardabili, Faculty of Agriculture and Natural Resources, Department of Plant Protection, Ardabil, Iran.

3 Associate professor, Agricultural Research, Education and Extension Organization (AREEO), Iranian Research Institute of Plant Protection, Biological Control Research Department, Tehran, Iran.

10.22092/bcpp.2025.370170.392

Abstract

The greenhouse whitefly, Trialeurodes vaporariorum (Westwood), is one of the most important pests of greenhouse crops worldwide. In the present study, the biology and age–stage, two–sex life table parameters of the parasitoid wasp Encarsia formosa Gahan were evaluated using second–instar nymphs of T. vaporariorum reared on three economically important greenhouse crops; eggplant (Solanum melongena), cucumber (Cucumis sativus), and tomato (Solanum lycopersicum). Experiments were conducted under controlled environmental conditions of 25 ± 2 °C, 65 ± 10% relative humidity, and a photoperiod of 16:8 h (L: D). Means and standard errors were estimated using the bootstrap method with 100,000 replications. The results revealed statistically significant differences in the mean biological traits and demographic parameters of E. formosa across the three host plant species. The total preadult duration on eggplant, cucumber, and tomato was 17.77 ± 0.18, 15.67 ± 0.15, and 14.97 ± 0.13 days, respectively. The longevity of adult females on the mentioned plant hosts was 20.21 ± 1.03, 24.64 ± 1.36, and 19.03 ± 0.69 days, while the mean fecundity per female was 129.38 ± 4.95, 104.24 ± 3.67, and 166.16 ± 6.31 eggs, respectively. The intrinsic rate of increase (r) on eggplant, cucumber, and tomato was 0.198 ± 0.004, 0.208 ± 0.004, and 0.239 ± 0.004 day⁻¹, respectively. The net reproductive rate (R0) was calculated to be 109.98 ± 9.44, 92.97 ± 6.57, and 142.29 ± 11.08 on the mentioned plant hosts, respectively. Overall, tomato was identified as the most suitable host plant among those tested, supporting faster development and higher reproductive output of E. formosa. These findings suggest that host plant species significantly influence the performance of E. formosa and should be considered when implementing biological control strategies against T. vaporariorum in greenhouse cropping systems.
.

Keywords

Main Subjects


Abai, M. 2010. Pests of Forest Trees and Shrubs of Iran. 1st ed. AREEO Publication, 178 Pages. (In Persian)
Abbasipour, H., Zeinolabedin Fard, N. & Saeedizadeh, A. 2017. Comparison of entomopathogenic nematodes efficacy on control of the Elm–Leaf Beetle, Xanthogaleruca luteola Müller )Col.: Chrysomelidae( in vitro. 2nd Iranian International Congress of Entomology, 2–4 September. Karaj. Iran.
Alford, D.V. 2012. Pests of Ornamentals Trees, Shrubs and Flowers. CRC Press, Manson Publishing Ltd, London.
Arbab, A., Sahragard, A. & Jalali Sendi, J. 2002. Laboratory investigation on Elm Leaf Beetle Xanthogaleruca luteola Muller (Col.: Chrysomelidae) biology. Journal of Entomological Society of Iran, 21: 73–85. (In Persian with English Summary).
Berry, R.E. & DeAngelis, J.D. 2000. Insect control on nursery and landscape plants with entomopathogens. pp. 629–650 In: Lacey, L.A. & Kaya H.K. )eds.), Field Manual of Techniques in Invertebrate Pathology. Springer Science.
Coyle, D.R., McMillin, J.D., Krause, S.C. & Hart, E.R. 2000. Laboratory and field evaluations of two Bacillus thuringiensis formulations, Novodor and Raven, for control of cottonwood leaf beetle (Coleoptera: Chrysomelidae). Journal of Economic Entomology, 93(3): 713–720.
Cranshaw, W.S., Day, S.J., Gritzmacher, T.J. & Zimmerman, R.J. 1989. Field and laboratory evaluations of Bacillus thuringiensis strains for control of elm leaf beetle. Journal of Arboriculture, 15: 31–34.
Dahlsten, D.L., Rowney, D.L. & Tait, S.M. 1994. Development of integrated pest management programs in urban forests: the elm beetle (Xanthogaleruca luteola (Müller)) in California, USA. Forest Ecology and Management, 65: 31–44.
Francardi, V. 1990. Results in the use of a new microbiological preparation based on Bacillus thuringiensis var. tenebrionis in the control of the larvae of Pyrrhalta luteola (Mull). Redia, 73: 463–472.
Gaugler, R. 2002. Entomopathogenic Nematology, CABI Publishing, 388 pages.
Giayetto, A.L. & Cichón, L.I. 2006. Distribución, gama de huéspedes y especificidad de cinco poblaciones de Heterorhabditis bacteriophora (NEMATODA: HETERORHABDITIDAE) del Alto Valle de Río Negro y Neuquén, Argentina. Revista de Investigaciones Agropecuarias, 35(2): 163–183.
Hajialiloobonab, S., Moravej, G. & Haidari Latibari, M. 2017. Comparative study on the effect of Bacillus thuringiensis var. tenebrionis on adult and third instar larva of elm leaf beetle, Xanthogaleruca luteola )Mull( under laboratory and field conditions. Proceedings of the 8th Biolical control conference. 1–2 November, Rasht, Iran., P. 7. )In Persian with English Summary(.
Hajialiloobonab, S., Moravej, G. & Sadeghi Namaghi, H. 2016. Comparative study on the efficacy of Bacillus thuringiensis var. tenebrionis and a neem based insecticide on adults and larvae of Xanthogaleruca luteola )Mull( )Col: Chrysomelidae( in laboratory conditions. Journal of Entomology and Zoology Studies, 4)4(: 1122–1125.
Haji Allahverdipour, H. 2025. Potential of entomopathogenic nematodes and Bacillus thuringiensis in control of Elm Leaf Beetle Xanthogaleruca luteola. Final Report Project. ISBN: 67432, Agricultural Research, Education, Extension Organization, 30 Pages. (In Persian with English Summery).
Haji Allahverdipour, H. & Marzban, R. 2023. Efficacy assessment of the nematode Steinernema carpocapsae and the bacterium Bacillus thuringiensis in control of Elm Leaf Beetle, (Xanthogaleruc luteola) under laboratory conditions. Plant Protection (Scientific Journal of Agriculture), 46(1): 25–37.
James, R.R., Croft, B.A. & Strauss, S.H. 1999. Susceptibility of the Cottonwood Leaf Beetle (Coleoptera: Chrysomelidae) to different strains and transgenic toxins of Bacillus thuringiensis. Environmental Entomology, 28(1): 108–115.
Jisha, V.N., Smitha, R.B. & Benjamin, S. 2013. An overview on the crystal toxins from Bacillus thuringiensis. Advances in Microbiology, 3(05): p. 462.
Jung, S. & Kim, Y. 2006. Synergistic effect of entomopathogenic bacteria (Xenorhabdus sp. and Photorhabdus temperata ssp. temperata) on the pathogenicity of Bacillus thuringiensis ssp. aizawai against Spodoptera exigua (Lepidoptera: Noctuidae). Environmental Entomology, 35(6): 1584–1589.
Kalyuzhnaya, N.S., Gorbacheva, O.V. & Didyk, L.K. 1995. Galerucella luteola Müll. )Coleoptera, Chrysomelidae( as a pest of plantations of trees in the southern Ergeni Hills )Kalmykia(. Ėntomologicheskoe Obozrenie, 74)1(: 45–51.
Kaya, H.K., Hara, A.H. & Reardon, R.C. 1981. Laboratory and field evaluation of Neoaplectana carpocapsae (Rhabditida: Steinernematidae) against the elm leaf beetle (Coleoptera: Chrysomelidae) and the western spruce budworm (Lepidoptera: Torthcidae). Canadian Entomologist, 113: 787–793.
Li, Y. & Wu, S.Y. 2024. Entomopathogenic nematodes in insect pest biocontrol: Diversity and function of excretory/secretory proteins. Journal of Invertebrate Pathology, 207: 108205.
Ma, X., Hu, J., Ding, C. Portieles, R., Xu, H., Gao, J., Du, L., Gao, X., Yue, Q., Zhao, L. & Borrás–Hidalgo, O. 2023. New native Bacillus thuringiensis strains induce high insecticidal action against Culex pipiens pallens larvae and adults. BMC Microbiology, 23: 100.
Memari, Z. 2016. Study on the effect of entomopathogenic nematodes on Ectomyelois ceratoniae Zeller )Lep. Pyralidae( [MSc thesis, Ferdowsi University of Mashhad].
Osman, G.E.H., El–Ghareeb, D., Already, R., Assaeedi, A.S.A., Organji, S.R., Abulreesh, H.H. & Althubiani, A.S. 2015. Bioinsecticide Bacillus thuringiensis a comprehensive review. Egyptian Journal of Biological Pest Control, 25(1): 271–288.
Saberi, F., Marzban, R., Ardjmand, M., Pajoum Shariati, F. & Tavakoli, O. 2020. Optimization of culture media to enhance the ability of local Bacillus thuringiensis var. tenebrionis. Journal of the Saudi Society of Agricultural Sciences, 19)7(: 468–475.
Sato, K., Kadota, Y. & Shirasu, K. 2019. Plant immune responses to parasitic nematodes. Frontiers in Plant Science, 10: 1165.
Sieiro, C., Pichardo–Gallardo, Á., Areal–Hermida, L., Almuiña–González, R. & Villa, T.G. 2021. Parasporal crystal toxins in Bacillus thuringiensis. pp. 125–148. In: Villa, T.G. & deMiguel Bouzas, T. (eds.), Developmental Biology in Prokaryotes and Lower Eukaryotes. Cham: Springer International Publishing.
Tenczar, E.G. & Krischik, V.A. 2006. Management of Cottonwood Leaf Beetle (Coleoptera: Chrysomelidae) with a novel transplant soak and biorational insecticides to conserve Coccinellid beetles, Journal of Economic Entomology, 99(1): 102–108.
Thurston, G.S. 2001. Xanthogaleruca luteola (Muller), Elm Leaf Beetle (Coleoptera: Chrysomelidae). pp. 272–274. In: Mason, P.G. & Huber, J.T. (eds.), Biological Control Programmes in Canada, 1981–2000. CABI.
Toscano, A. 2019. Parasite–host relationships in the biological control of insects: strategies of immunoevasion/immunosuppression and interference of temperature on the lethality of entomoparasites. PhD Thesis. Available at https://irinsubria.uninsubria.it/handle/11383/2090711#
Wells, A.J., Kwong, R.M. & Field, R. 1994. Elm leaf beetle control using the biological insecticide, Novodor )Bacillus thuringiensis subsp. tenebrionis(. Plant Protection Quarterly, 9: 52–55.
Zeinolabedin Fard, N., Abbasipour, H., Saeedizadeh, A. & Karimi, J. 2020. Laboratory assay of entomopathogenic nematodes against the elm leaf beetle, Xanthogaleruca luteola Müller )Col.: Chrysomelidae(. Journal of Forest Science, 66: 524–531.
Zhang, Q., Gang, H. & Adang, M.J. 2017. Effects and mechanisms of Bacillus thuringiensis crystal toxins for mosquito larvae. Insect Science, 24(5): 714–729.
Zou, H., Gu, H., Cheng, J., Tian, C., Shu, Q., Peng, P. & Li, B. 2024. The mechanism of damage to the midgut by low concentration of Bacillus thuringiensis in the Silkworm, Bombyx mori. Insects, 15(12): 911.