[en] Encarsia sophia is the dominant parasitoid of invasive whitefly pest such as Bemisia tabaci. This heteronomous hyperparasitoid species lays fertilised diploid eggs in whitefly nymphs, which serve as primary hosts. Larvae develop as female progeny by consuming whitefly hosts, providing direct biocontrol benefits. However, male progeny originate from unfertilised eggs laid on secondary hosts (primary parasitoids within whitefly nymphs) and develop by consuming primary parasitoid larvae rather than whitefly hosts. Therefore, it is crucial for indoor rearing and field release of the hyperparasitoid to determine whether a female with single-mating experience can parasitise primary hosts and produce female progeny for a whole lifetime and, if not, whether it is remating events and prolong the period of female production, thereby increasing the amount of parasitism on whiteflies. Our fecundity experiments of females with single-mating experience, equally provided with primary and secondary hosts, showed that single mating was insufficient for E. sophia females to lay fertilised eggs in whitefly nymphs for their whole lifetime. In multiple mating experiments, 76.7 % of male adults completed their second mating 2 h after the first, whereas female adults accepted the second mating only if primary hosts were available thereafter. Remating was beneficial for female adults as it prolonged the ovipositional period of fertilised eggs (from 13.3 ± 0.6 days for single to 17.1 ± 0.7 days for twice mating) and increased parasitism on B. tabaci primary host (from 53.1 ± 3.8 for single to 76.4 ± 5.9 for twice mating respectively). The mating experience of males increased their copulation success, whereas that of females decreased it. In conclusion, recommendations are provided for large-scale indoor rearing and field release of E. sophia. Firstly, sufficient time for providing males can be shortened to within 2 h, and a single male can engage in 2–3 mating sessions. Following the 15-day peak oviposition period, the addition of newly emerged males is advised. Secondly, for field release of adult parasitoids, it is recommended to concentrate on releasing females after completing mating indoors. For the release of pupae cards, ensure a balanced ratio of males and females on each card to facilitate mating upon emergence. Additionally, release extra males and females 2 weeks after the initial batch of releases.
Disciplines :
Entomology & pest control
Author, co-author :
Man, Xiaoming ; Université de Liège - ULiège > TERRA Research Centre ; State Key Laboratory for Biology of Plant Diseases and Insect Pests, Institute of Plant Protection, Chinese Academy of Agricultural Sciences, Beijing, China
Sun, Li-Ying; State Key Laboratory for Biology of Plant Diseases and Insect Pests, Institute of Plant Protection, Chinese Academy of Agricultural Sciences, Beijing, China
Francis, Frédéric ; Université de Liège - ULiège > TERRA Research Centre > Gestion durable des bio-agresseurs
Yang, Nian-Wan; State Key Laboratory for Biology of Plant Diseases and Insect Pests, Institute of Plant Protection, Chinese Academy of Agricultural Sciences, Beijing, China ; Western Agricultural Research Center, Chinese Academy of Agricultural Sciences, Changji, China
Liu, Wan-Xue; State Key Laboratory for Biology of Plant Diseases and Insect Pests, Institute of Plant Protection, Chinese Academy of Agricultural Sciences, Beijing, China
Language :
English
Title :
Benefits of remating of a hyperparasitoid acting as a biocontrol agent
NSCF - National Natural Science Foundation of China
Funding text :
We would like to thank Dr. Shagufta-Rani Khanzada for her practical advice in Encarsia sophia mating selection experiments. This work was supported by the National Natural Science Foundation of China (32072493) and National Key R&D Program of China (2021YFC2600400).
Arnqvist, G., Nilsson, T., The evolution of polyandry: multiple mating and female fitness in insects. Anim Behav. 60 (2000), 145–164, 10.1006/anbe.2000.1446.
Avilla, J., Copland, M.J.W., Effects of host stage on the development of the facultative autoparasitoid Encarsia tricolor (Hymenoptera: Aphelinidae). Ann Appl Biol 110 (1987), 381–389, 10.1111/j.1744-7348.1987.tb03269.x.
Boomsma, J., Split sex ratios and queen-male conflict over sperm allocation. Proc. Royal Soc. b. 263 (1996), 697–704, 10.1098/rspb.1996.0104.
Bressac, C., Chevrier, C., Offspring and sex ratio are independent of sperm management in Eupelmus orientalis females. J. Insect Physiol. 44 (1998), 351–359, 10.1016/S0022-1910(97)00119-4.
Chang, Y. D., & Kang, L., 2002. Strategies used by male and female insects in multiple mating behavior and sperm competition. Acta Entomologica Sinica, 45, 833-839. 10.16380/j.kcxb.2002.06.021.
Chapman, T., Liddle, L.F., Kalb, J.M., et al. Cost of mating in Drosophila melanogaster females is mediated by male accessory gland products. Nature (London) 373 (1995), 241–244, 10.1038/373241a0.
Chapman, T., Göran, A., Bangham, J., et al. Sexual conflict. Trends Ecol. Evol. 18 (2003), 41–47, 10.1016/S0169-5347(02)00004-6.
Chevrier, C., Bressac, C., Sperm Storage and Use After Multiple Mating in Dinarmus basalis (Hymenoptera: Pteromalidae). J. Insect. Behav. 15 (2002), 385–398, 10.1023/A:1016269210140.
Cloutier, C., Duperron, J., Tertuliano, M., et al. Host instar, body size and fitness in the koinobiotic parasitoid Aphidius nigripes. Entomol. Exp. Appl. 97 (2010), 29–40, 10.1023/A:1004056818645.
De Barro, P.J. 1995. Bemisia tabaci biotype B: a review of its biology, distribution and control. Commonwealth Scientific and Industrial Research Organization, Canberra, ACT, Australia. https://api.semanticscholar.org/CorpusID:89854884.
Duplouy, A., Woestmann, L., Gallego-Zamorano, J., et al., Impact of male condition on his spermatophore and consequences for female reproductive performance in the Glanville fritillary butterfly. Insect Sci. 25, 284-296. 10.1111/1744-7917.12424.
Engqvist, L., Nuptial food gifts influence female egg production in the scorpionfly Panorpa cognata. Ecol Entomol. 32 (2007), 327–332, 10.1111/j.1365-2311.2006.00835.x.
Fedorka, K.M., Mousseau, T.A., Material and genetic benefits of female multiple mating and polyandry. Anim. Behav. 64 (2002), 361–367, 10.1006/anbe.2002.3052.
Gabriela, P.L., Reproductive costs of mating with a sibling male: Sperm depletion and multiple mating in Cephalonomia hyalinipennis. Entomol. Exp. Appl. 137 (2010), 62–72, 10.1111/j.1570-7458.2010.01037.x.
Gerling, D., Status of Bemisia tabaci in the Mediterranean countries: opportunities for biological control. Biol. Control 6 (1996), 11–22, 10.1006/bcon.1996.0002.
Global Biodiversity Information Facility (GBIF). 2017. http://www.gbif.org/species/1365395.
Hayashi, F., Multiple mating and lifetime reproductive output in female dobsonflies that receive nuptial gifts. Ecol Res. 13 (1998), 283–289, 10.1046/j.1440-1703.1998.00272.x.
Heraty, J.M., Polaszek, A.P., Morphometric analysis and descriptions of selected species in the Encarsia strenua group (Hymenoptera: Aphelinidae). J. Hymenopt. Res. 9 (2000), 142–169.
Hoelmer, K., Goolsby, J., Release, establishment and monitoring of Bemisia tabaci natural enemies in the United States. Proceedings of the 1st International Symposium on Biological Control of Arthropods, 2002, 14–18.
Hosken, D., Stockley, P., Benefits of polyandry: A life history perspective. Evol Biol 33 (2003), 173–194 http://iucn.org/themes/ssc/pubs/policy/invasivesEng.htm.
Hunter, M., Woolley, J., Evolution and behavioral ecology of heteronomous aphelinid parasitoids. Annu. Rev. Entomol. 46 (2001), 251–290, 10.1146/annurev.ento.46.1.251.
Jennions, D., Petrie, M., Why do females mate multiply? A review of the genetic benefits. Biol. Rev. 75 (2000), 21–64, 10.1017/S0006323199005423.
Jian, Z., Animal behavior principle and species protection method. 2004, Science Press.
King, B., Mate Location and the Onset of Sexual Responsiveness in the Parasitoid Wasp Spalangia endius(Hymenoptera: Pteromalidae). Environ. Entomol. 35 (2010), 1390–1395, 10.1093/ee/35.5.1390.
King, B., Kuban, K., Should he stay or should he go: male influence on offspring sex ratio via postcopulatory attendance. Behav. Ecol. Sociobiol. 66 (2012), 1165–1173, 10.1007/s00265-012-1369-5.
Liu, X., He, H., Kuang, X., et al. Factors influencing mating duration in the cabbage beetle, Colaphellus bowringi Baly (Coleoptera: Cerambycidae). Acta Entomol. Sin. 53 (2010), 549–554, 10.1016/S1002-0721(10)60377-8.
Liu, B., Li, M., Xiong, Y., et al. Mating behavior of Trichopria drosophilae and the effect of male mating frequency on the production of female offspring. Chin. J. Appl. Entomol. 54 (2017), 749–754 http://www.ent-bull.com.cn/admin/downfile.aspx?id=54807.
Maynard-Smith, J., The evolution of sex. Genet. Res. 32 (1978), 1–9, 10.1017/S0016672300018693.
Mery, F., Joly, D., Multiple mating, sperm transfer and oviposition pattern in the giant sperm species, Drosophila bifurca. Evol. Biol. 15 (2002), 49–56, 10.1046/j.1420-9101.2002.00364.x.
Nakamura, M., Multiple mating and cooperative breeding in polygynandrous alpine accentors.II. Male Mating Tactics. Anim. Behav. 55 (1998), 277–289, 10.1006/anbe.1997.0599.
Nason, S., Kelly, C., Benefits of multiple mating in a sexually dimorphic polygynandrous insect. Anim. Behav. 164 (2020), 65–72, 10.1016/j.anbehav.2020.03.018.
Oliveira, M., Henneberry, T., Anderson, P., History, current status, and collaborative research projects for Bemisia tabaci. Crop Prot. 20 (2001), 709–723, 10.1016/S0261-2194(01)00108-9.
Pai, A., Bennett, L., Yan, G., Female multiple mating for fertility assurance in red flour beetles (Tribolium castaneum). Can. J. Zool. 83 (2005), 913–919, 10.1139/z05-073.
Passera, L., Keller, L., The period of sexual maturation and the age at mating in Iridomyrmex humilis, an ant with intranidal mating. Zoology 228 (1992), 141–143, 10.1111/j.1469-7998.1992.tb04438.x.
Polaszek, A., Evans, G.A., Bennett, F.D., Encarsia parasitoids of Bemisia tabaci (Hymenoptera: Aphelinidae, Homoptera: Aleyrodidae): A preliminary guide to identification. Bull. Entomol. Res 82 (1992), 375–392, 10.1017/S0007485300041171.
Ridley, Mark, Clutch size and mating frequency in parasitic hymenoptera. Am. Nat. 142 (1993), 893–910, 10.1086/285579.
Simmons, L., The evolution of polyandry: an examination of the genetic incompatibility and good-sperm hypotheses. J. Evol. Biol., 14, 2001, 10, 10.1046/j.1420-9101.2001.00309.x.
Snook, R., Sexual selection: Conflict, kindness and chicanery. Curr. Biol., 11, 2001, 10.1016/S0960-9822(01)00188-9.
Steiner, S., Henrich, N., Ruther, J., Mating with sperm-depleted males does not increase female mating frequency in the parasitoid Lariophagus distinguendus. Entomol. Exp. Appl. 126 (2010), 131–137, 10.1111/j.1570-7458.2007.00641.x.
Sun, F., Chen, Z., Duan, B., et al. Mating behavior of Pachycrepoideus vindemmiae Rondani and the effects of male mating times on the production of females. Acta Ecol. Sin. 33 (2013), 4354–4360, 10.5846/stxb201210221465.
Vahed, K., All that Glisters is not Gold: Sensory Bias, Sexual Conflict and Nuptial Feeding in Insects and Spiders. Ethology 113 (2007), 105–127, 10.1111/j.1439-0310.2006.01312.x.
Walter, G., Divergent Male Ontogenies in Aphelinidae (hymenoptera, Chalcidoidea) - a Simplified Classification and a Suggested Evolutionary Sequence. Biol. J. Linn. Soc. Lond. 19 (1983), 63–82, 10.1111/j.1095-8312.1983.tb00777.x.
Wan, F., Yang, N., Invasion and Management of Agricultural Alien Insects in China. Annu. Rev. Entomol. 61 (2016), 77–98, 10.1146/annurev-ento-010715-023916.
Wang, S., Wang, L., Liu, J., et al. Multiple Mating of Aphelinus asychis Enhance the Number of Female Progeny but Shorten the Longevity. Insects., 12, 2021, 823, 10.3390/insects12090823.
Wedell, N., Ritchie, M.G., Male age, mating status and nuptial gift quality in a bushcricket. Anim Behav. 67 (2004), 1059–1065, 10.1016/j.anbehav.2003.10.007.
Wedell, N., Tregenza, T., Benefits of Multiple Mates in the Cricket Gryllus bimaculatus. Evolution 52 (1988), 1726–1730, 10.1111/j.1558-5646.1998.tb02252.x.
Wiklund, L.S., Prolonged Mating in the Monarch Butterfly Danaus plexippus and Nightfall as a Cue for Sperm Transfer. Oikos 51 (1988), 351–354, 10.2307/3565317.
Xia, J., Guo, Z., Yang, Z., et al. Whitefly hijacks a plant detoxification gene that neutralizes plant toxins. Cell 184 (2021), 1693–1705, 10.1016/j.cell.2021.02.014.
Xu, H., Yang, N., Wan, F., Competitive interactions between parasitoids provide new insight into host suppression. PLoS One, 8, 2013, e82003.
Xu, H., Yang, N., Chi, H., et al. Comparison of demographic fitness and biocontrol effectiveness of two parasitoids, Encarsia sophia and Eretmocerus hayati (Hymenoptera: Aphelinidae), against Bemisia tabaci (Hemiptera: Aleyrodidae). Pest Manag. Sci. 74 (2018), 2116–2124, 10.1002/ps.4908.
Yang, N., Wan, F., Host suitability of different instars of Bemisia tabaci biotype B for the parasitoid Eretmocerus hayati. Biol. Control. 59 (2011), 313–317, 10.1016/j.biocontrol.2011.07.019.
Yang, N., Ji, L., Lovei, G., et al. Shifting preference between oviposition vs. host- feeding under changing host densities in two aphelinid parasitoids. PLoS One, 7, 2012, e41189.
Zang, L., Liu, T., Wan, F., Reevaluation of the Value of Autoparasitoids in Biological Control. PLoS One, 6, 2011, e20324.
Zeh, J., Zeh, D., Toward a new sexual selection paradigm: Polyandry, conflict and incompatibility. Ethology 109 (2010), 929–950, 10.1046/j.1439-0310.2003.00945.x.
Zhang, Y., Lu, Y., Sai, D., Sexual selection research of Atractomorpha sinens. J. Shangdong Normal Univ. 24 (2009), 128–130.
Zou, M., Liu, L., Dong, S., et al., 2022. Effects of multiple mating on the spermatophore formation and fecundity of Plutella xylostella (Lepidoptera: Plutellidae). Acta Entomologica Sinica, 65, 1678-1686. 10.16380/j.kcxb.2022.12.013.