Host selection for the mass production of Trichogrammatoidea cryptophlebiae (Nagaraja, 1979) (Hymenoptera: Trichogrammatidae)
DOI:
https://doi.org/10.17159/2254-8854/2026/a23744Keywords:
choice assays, Cryptophlebia peltastica, Lobesia vanillana, no-choice assays, mass-rearing, tortricidaeAbstract
The generalist egg parasitoid Trichogrammatoidea cryptophlebiae (Nagaraja, 1979) (Hymenoptera: Trichogrammatidae) is mass-reared in South Africa on Thaumatotibia leucotreta (false codling moth). However, alternative tortricid hosts may improve or enhance production. This study assessed the suitability of Cydia pomonella, Cryptophlebia peltastica and Lobesia vanillana as alternative hosts for the parasitoid through no-choice and choice trials. Host acceptance, emergence, superparasitism, unsuccessful emergence, sex ratio, and offspring morphology were measured. In no-choice assays, T. leucotreta and L. vanillana yielded the highest parasitism, while C. peltastica showed significantly less parasitism. Emergence was highest from C. pomonella and C. peltastica, but high superparasitism in these species resulted in increased unsuccessful development compared to the other species. Lobesia vanillana, the smallest host, classified by egg size, produced significantly smaller offspring of the parasitoid. Morphological analyses showed limited differences in forewing length, but significant host- and sex-dependent variation in hind tibia length. Choice trials revealed a consistent preference for T. leucotreta, particularly eggs that had been irradiated, suggesting its continued suitability for mass production of T. cryptophlebiae. These findings highlight key host-related traits affecting T. cryptophlebiae biology and rearing potential and confirm L. vanillana and C. peltastica as physiological hosts.
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References
Bioresources (Pty) Ltd. 2023. MacTrix- Trichogramma Wasps. Accessed: 24 October 2023. Bioresources (Pty) Ltd. https://bioresources.com.au/good-bugs/mactrix-wasps/
Bjorksten TA, Hoffman AA. 1998. Separating the effects of experience, size, egg load, and genotype on the host response in Trichogramma (Hymenoptera: Trichogrammatidae). Journal of Insect Behaviour. 11(1):129–148. https://doi.org/10.1023/A:1020826818884. DOI: https://doi.org/10.1023/A:1020826818884
Carpenter JE, Bloem S, Hofmeyr JH. 2004. Acceptability and suitability of eggs of false codling moth (Lepidoptera: Tortricidae) from irradiated parents to parasitism by Trichogrammatoidea cryptophlebiae (Hymenoptera: Trichogrammatidae). Biological Control. 30:351–359. https://doi.org/10.1016/j.biocontrol.2003.10.006. DOI: https://doi.org/10.1016/j.biocontrol.2003.10.006
Chambers BA, Samways MJ, Ironside DA. 1995. Egg distribution of the fruit borers Cryptophlebia leucotreta (Meyrick) and C. batrochopa (Meyrick) (Lepidoptera: Tortricidae) and their egg parasitoid Trichogrammatoidea cryptophlebiae Nagaraja (Hymenoptera: Trichogrammatidae) in macadamia trees in Malawi. African Entomology. 3(2):181–188.
Cherif A, Mansour R, Grissa-Lebdi K. 2021. The egg parasitoids Trichogramma: from laboratory mass rearing to biological control of lepidopteran pests. Biocontrol Science and Technology. 31(7):661–693. https://doi.org/10.1080/09583157.2020.1871469. DOI: https://doi.org/10.1080/09583157.2020.1871469
Githae MM, Coombes CA, Mutamiswa R, Moore SD, Hill MP. 2024.Suitability of false codling moth eggs from different sterile to fertile moth ratios in the sterile insect technique programme, to parasitism by Trichogrammatoidea cryptophlebiae. Crop Protection. 182:106744. https://doi.org/10.1016/j.cropro.2024.106744. DOI: https://doi.org/10.1016/j.cropro.2024.106744
Grenier S, Grille G, Basso C, Pintureau B. 2001. Effects of the host species and the number of parasitoids per host on the size of some Trichogramma species (Hymenoptera: Trichogrammatidae). Biocontrol Science and Technology. 11:21–26. https://doi.org/10.1080/09583150020029709. DOI: https://doi.org/10.1080/09583150020029709
Iranipour S, Vaez N, Ghanbalani GN, Zakaria RA, Jafarloo MM. 2010. Effect of host change on demographic fitness of the parasitoid, Trichogramma brassicae. Journal of Insect Science. 10(78):1–12. https://doi.org/10.1673/031.010.7801. DOI: https://doi.org/10.1673/031.010.7801
Kaspi R, Steinitz H, Nemny-Lavi E, Lebedev G, Melamed E, Gazit Y. 2020. Nontarget host risk assessment of the egg parasitoid Trichogrammatoidea cryptophlebiae (Hymenoptera: Trichogrammatidae) for classical biological control of the false codling moth (Lepidoptera: Tortricidae) in Israel. Journal of Economic Entomology. 113(2):1023–1027. https://doi.org/10.1093/jee/toz327. DOI: https://doi.org/10.1093/jee/toz327
Le Ralec A, Rabasse JM, Wajnberg E. 1996. Comparative morphology of the ovipositor of some parasitic Hymenoptera in relation to characteristics of their hosts. The Canadian Entomologist. 128:413–433. https://doi.org/10.4039/Ent128413-3. DOI: https://doi.org/10.4039/Ent128413-3
Liu S, Yan Z-C, Zhou F-W, Wang C-X, Li Y-X. 2024. Relationship between parasitism and morphology of Trichogramma (Hymenoptera: Trichogrammatidae) on Spodoptera frugiperda (Lepidoptera: Noctuidae). Journal of Economic Entomology. 117(1):93–101. https://doi.org/10.1093/jee/toad231. DOI: https://doi.org/10.1093/jee/toad231
Luo T-I, Wang Z-Y, Wei X, Jiang Y-T, Xu K, Jiang K, Qui L-F, Hu H-Y, Liu P-C. 2025. Preferentially laying female offspring during self-superparasitism in a quasigregarious parasitoid. Animal Behaviour. 224:123205. https://doi.org/10.1016/j.anbehav.2025.123205. DOI: https://doi.org/10.1016/j.anbehav.2025.123205
Luck RF, Janssen JAM, Pinto JD, Oatman ER. 2001. Precise sex allocation, local mate competition, and sex ratio shifts in the parasitoid Trichogramma pretiosum. Behavioral Ecology and Sociobiology. 49:311–321. https://doi.org/10.1007/s002650000294. DOI: https://doi.org/10.1007/s002650000294
Martel V, Darrouzet E, Boivin G. 2011. Phenotypic plasticity in the reproductive traits of a parasitoid. Journal of Insect Physiology. 57:682–687. https://doi.org/10.1016/j.jinsphys.2011.01.018. DOI: https://doi.org/10.1016/j.jinsphys.2011.01.018
Moore SD, Fourie J. 1999. Assessment and development of the augmentation technique for FCM control with the parasitoid Trichogrammatoidea cryptophlebiae. Experiment 401. 1–9.
Moore SD, Richards GI. 2000. Assessment and development of the augmentation technique for FCM control with the parasitoid Trichogrammatoidea cryptophlebiae. Experiment 401. 1–6.
Moore SD, Richards GI. 2001. Assessment and development of the augmentation technique for FCM control with the parasitoid Trichogrammatoidea cryptophlebiae. Project: FCM, Experiment 401. 1–13.
Moore SD, Richards GI. 2002. Assessment and development of the augmentation technique for FCM control with the parasitoid Trichogrammatoidea cryptophlebiae. Experiment 401. 1–9.
Moore SD, Kirkman W, Mommsen W, Beetge L, Otto H. 2015. Late-season releases of Trichogrammatoidea cryptophlebiae for suppression of FCM. Final Report, Project 1021. 1–16.
Nagaraja H. 1978. Studies on Trichogrammatoidea (Hymenoptera: Trichogrammatidae). Oriental Insects. 12(4):489–529. https://doi.org/10.1080/00305316.1978.10432534. DOI: https://doi.org/10.1080/00305316.1978.10432534
Leppla NC, Morales-Ramos JA, Shapiro-Ilan D, Guadalupe Rojas M. 2023. Introduction. In: Morales-Ramos JA, Guadalupe Rojas M, Shapiro-Ilan D, editors. Mass Production of Beneficial Organisms. 2nd edition. London, United Kingdom: Academic Press; pp. 3–12. https://doi.org/10.1016/B978-0-12-822106-8.00007-5. DOI: https://doi.org/10.1016/B978-0-12-822106-8.00007-5
Newton PJ. 1988a. Movement and impact of Trichogrammatoidea cryptophlebiae Nagaraja (Hymenoptera: Trichogrammatidae) in citrus orchards after inundative releases against the false codling moth, Cryptophlebia leucotreta (Meyrick) (Lepidoptera: Tortricidae). Bulletin of Entomological Research. 78:85–99. https://doi.org/10.1017/S0007485300016096. DOI: https://doi.org/10.1017/S0007485300016096
Newton PJ. 1988b. Inversely density-dependent egg parasitism in patchy distributions of the citrus pest Cryptophlebia leucotreta (Lepidoptera: Tortricidae) and its agricultural efficiency. Journal of Applied Ecology. 25:145–162. https://doi.org/10.2307/2403615. DOI: https://doi.org/10.2307/2403615
Newton PJ. 1989. Combinations of applications of a chitin synthesis inhibitor and inundative releases of egg parasitoids against the false codling moth, Cryptophlebia leucotreta (Meyrick) (Lepidoptera: Tortricidae), on citrus. Bulletin of Entomological Research. 79:507–519. https://doi.org/10.1017/S0007485300018472. DOI: https://doi.org/10.1017/S0007485300018472
Newton PJ, Crause C. 1990. Oviposition on Litchi chinensis by Cryptophlebia species (Lepidoptera: Tortricidae). Phytophylactica. 22(3):365–367.
Newton PJ, Odendaal WJ. 1990. Commercial inundative releases of Trichogrammatoidea cryptophlebiae (Hym: Trichogrammatidae) against Cryptophlebia leucotreta (Lepidoptera: Tortricidae) in Citrus. Entomophaga. 35(4):545–556. https://doi.org/10.1007/BF02375089. DOI: https://doi.org/10.1007/BF02375089
Nordlund DA, Wu ZX, Greenberg SM. 1997. In Vitro rearing of Trichogramma minutum Riley (Hymenoptera: Trichogrammatidae) for ten generations, with quality assessment comparisons of in Vitro and in Vivo reared adults. Biological Control. 9:201–207. https://doi.org/10.1006/bcon.1997.0534. DOI: https://doi.org/10.1006/bcon.1997.0534
Pak GA, Van Dalen A, Kaashoek N, Dijkman H. 1990. Host egg chorion structure influencing host suitability for the egg parasitoid Trichogramma Westwood. Journal of Insect Physiology. 36(11):869–875. https://doi.org/10.1016/0022-1910(90)90174-E. DOI: https://doi.org/10.1016/0022-1910(90)90174-E
Parra JRP. 2010. Mass rearing of egg parasitoids for biological control programs. In: Cônsoli FL, Parra JRP, Zucchi RA, editors. Egg Parasitoids in Agroecosystems with Emphasis on Trichogramma. Dordrecht: Springer; pp. 267–292. DOI: https://doi.org/10.1007/978-1-4020-9110-0_10
Pehlivan S. 2021. Role of host diet on the fitness of the egg parasitoid species, Trichogramma evanescens Westwood (Hymenoptera: Trichogrammatidae). Egyptian Journal of Biological Pest Control. 31:a10. https://doi.org/10.1186/s41938-020-00353-7. DOI: https://doi.org/10.1186/s41938-020-00353-7
Perera MCD, Hemachandra KS. 2014. Study on longevity, fecundity and oviposition of Trichogrammatoidea bactrae Nagaraja (Hymenoptera: Trichogrammatidae) to facilitate mass rearing. Tropical Agricultural Research. 25(4):602–609. https://doi.org/10.4038/tar.v25i4.8065. DOI: https://doi.org/10.4038/tar.v25i4.8065
R Core Team. (2025). R: A language and environment for statistical computing. R Foundation for Statistical Computing. https://www.R-project.org/
Saour G. 2009. Effect of early oviposition experience on host acceptance in Trichogramma (Hymenoptera: Trichogrammatidae) and application of F1 sterility and T. principium to suppress the potato tuber moth (Lepidoptera: Gelechiidae). Biocontrol Science and Technology. 19(sup1):225–234. https://doi.org/10.1080/09583150802522838. DOI: https://doi.org/10.1080/09583150802522838
Suzuki Y, Tsuji H, Sasakawa M. 1984. Sex allocation and effects of superparasitism on secondary sex ratios in the gregarious parasitoid, Trichogramma chilonis (Hymenoptera: Trichogrammatidae). Animal Behaviour. 32:478–484. https://doi.org/10.1016/S0003-3472(84)80284-5. DOI: https://doi.org/10.1016/S0003-3472(84)80284-5
Tian JC, Wang ZC, Wang GR, Zhong LQ, Zheng XS, Xu HX, Zang, LS, Lu ZX. 2017. The effects of temperature and host age on the fecundity of four Trichogramma species, Egg parasitoids of the Cnaphalocrocis medinalis (Lepidoptera: Pyralidae). Journal of Economic Entomology. 110:949–953. https://doi.org/10.1093/jee/tox108. DOI: https://doi.org/10.1093/jee/tox108
Van Lenteren JC, Bolckmans K, Kohl J, Ravensberg WJ, Urbaneja A. 2018. Biological control using invertebrates and microorganisms: plenty of new opportunities. BioControl. 63:39–59. https://doi.org/10.1007/s10526-017-9801-4. DOI: https://doi.org/10.1007/s10526-017-9801-4
Van Lenteren JC, Hale A, Klapwijk JN, Van Schelt J, Steinberg S. 2003. Guidelines to quality control of commercially produced natural enemies. In: Van Lenteren JC, editor. Quality control and production of biological control agents: theory and testing procedures. Wageningen, The Netherlands: CABI Publishing; pp. 265–303. https://doi.org/10.1079/9780851996882.0265. DOI: https://doi.org/10.1079/9780851996882.0265
Xu J, Yang X, Ying L, Zang L-S, Tian C-Y, Ruan C-C. 2016. Effects of fertilized, unfertilized, and UV-irradiated hosts on parasitism and suitability for Trichogramma parasitoids. Entomologia Experimentalis et Applicata. 161:50–56. https://doi.org/10.1111/eea.12485. DOI: https://doi.org/10.1111/eea.12485
Zhang Y-H, Xue,J-Z, Tariq T, Li T-H, Qian H-Y, Cui W-H, Tian H, Monticelli LS, Desneux N, Zang L-S. 2024. Parasitism and suitability of Trichogramma chilonis on large eggs of two factitious hosts: Samia cynthia ricini and Antheraea pernyi. Insects. 15(1):2–11. https://doi.org/10.3390/insects15010002. DOI: https://doi.org/10.3390/insects15010002
Zhang Y, Zhu W, Mei W, Fan R, Wang J, Zhang J. 2024. Parasitoid fitness and quality of Corcyra cephalonica (Stainton) eggs after vacuum packaging combined with cold storage. Journal of Asia-Pacific Entomology. 27(1):102207. https://doi.org/10.1016/j.aspen.2024.102207. DOI: https://doi.org/10.1016/j.aspen.2024.102207
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