W.D. Hutchison1,2, E.K. Buchholz3, E.L. Meys4 and S. Wold-Burkness1
Dept. of Entomology, University of Minnesota1, UMN Extension Service2, UMN Landscape Arboretum3, & University of Illinois, Champaign-Urbana IL4
The Winsome Fly, Istocheta aldrichi (Mesnil, Diptera: Tachinidae), is a parasitoid of Japanese beetle (JB), Popillia japonica), which in recent years has become a significant economic pest of several Minnesota fruit crops (Ebbenga et al. 2023). In addition, with adult feeding damage to >300 host plants, JB is an ongoing pest of concern within urban gardens and ornamental plants and turf within the urban, residential landscapes in Minnesota. The Winsome fly (WF) was introduced as a biological control agent in 1923 in New Jersey, just 6 years after the accidental introduction of Japanese beetle (Shanovich et al. 2021, Althoff & Rice 2022). Since 1923, there have been numerous detections of WF in several Northeastern states and it is well established in Quebec and Ontario, Canada. WF is considered one of the more effective biological control agents for JB due to its potential impact on JB populations and its ability to adapt to a variety of climatic conditions (Potter & Held 2002, Shanovich et al. 2021, Althoff & Rice 2022).
Description & Life Cycle
Adult flies are small (5 mm), gray to beige, and about the same size as a housefly. Winsome flies emerge about a week before the Japanese beetles and feed on nectar-producing plants. Female flies seek out Japanese beetles and typically lay one egg just behind the head (pronotum) of the beetle. However, multiple eggs can be laid on one beetle, particularly when beetle populations are low. Eggs are pearly white and are easily seen. Within a few days of egg-lay, the parasitic larva will hatch, and with “serrated” mouthparts bore through the host cuticle and begin feeding. As the larvae develop through three instars, the beetle becomes increasingly lethargic, stops feeding in 3-4 days, and dies within 5-10 days. WF larvae typically pupate within the JB cadaver, and remains in the cadaver to overwinter. By mid- to late-June, the first WF adults emerge from the pupal stage, feed on floral nectar, mate and begin seeking JB adults for oviposition. There is only one generation per year.
History
During 1998 to 2006, several releases of WF (pupal stage) were made in Minnesota, by the USDA and Minn. Dept. of Agric. (MDA). The majority of WF were released at Theodore Wirth Park, Minneapolis. The first detections confirming establishment, by the MDA, were in 2004. Until recently, only low levels of WF parasitism had been reported in Minnesota, including 0.01-10% during 2017-2018 in Washington and Dakota county apple orchards (Shanovich et al. 2021). Although parasitism rates have been historically low in Minnesota, samples from the University of Minnesota’s Landscape Arboretum in 2022 confirmed a peak of 14-29% parasitism (E. Buchholz). In 2023, additional monitoring for WF found peak parasitism rates of 33-55% at the Arboretum, and 15-39% at 3 commercial vineyards (Hutchison et al. 2023). This recent experience generated new research in 2024 to further estimate the growing biocontrol impact of WF on JB populations in Minnesota. In addition, the results to date indicate that WF is adapting to Minnesota’s climate, including warmer winters, and that the fly's emergence phenology is better aligned with that of Japanese beetle emergence (also recently observed in Quebec, Canada; Gagnon et al. 2023).
Summary
As we continue to learn more about the geographic distribution and biology of WF in Minnesota, we will update this profile. Given the recent range expansion of WF in Minnesota and western Wisconsin, it appears this parasitoid is well positioned to continue to have a beneficial, biocontrol impact of JB, not only in urban, residential landscapes but also in several agricultural crops. Some of the higher parasitism rates to date have been recorded in commercial vineyards and apple orchards. More research is needed to better understand how WF mortality, and its impact on reducing JB female fecundity, can have long-term benefits for pest suppression.
Funding: This research was funded in part by a USDA-MDA Specialty Crop Block Grant, from 2021-2024.
Selected References
Althoff, E.R. & K.B. Rice. 2022. Japanese Beetle (Coleoptera: Scarabaeidae) invasion of North America: history, ecology, and management. J. Integ. Pest Mgmt. 13(1): 2, https://doi.org/10.1093/jipm/pmab043
Ebbenga, D., S.J. Wold-Burkness, E.C. Burkness, and W.D. Hutchison. 2023. Japanese Beetle: an Emerging Pest of Fruit Crops. FruitEdge. https://fruitedge.umn.edu/japanese-beetle/japanese-beetle-emerging-pest-fruit-crops
Gagnon, M-E., J. Doyon, S. Legault & J. Brodeur. 2023. The establishment of the association between the Japanese beetle (Coleoptera: Scarabaeidae) and the parasitoid Istocheta aldrichi (Diptera: Tachinidae) in Québec, Canada. The Canadian Entomol. 155: e32, 1-11.
Hutchison, B., E. Meys, & E. Buchholz. 2023. Long-term biological control of Japanese beetle: A Winsome Fly update. Minnesota Fruit & Vegetable News. https://blog-fruit-vegetable-ipm.extension.umn.edu/2023/08/long-term-biological-control-of.html
Pelletier, M., Legault, S., Doyon & J. Brodeur. 2023. Where and why do females of the parasitic fly, Istocheta aldrichi, lay their eggs on the body of adult Japanese beetles? J. Insect Behav. 36: 308–317. https://doi.org/10.1007/s10905-023-09841-8
Potter, D.A. & D.W. Held. 2002. Biology and management of the Japanese beetle. Ann. Rev. of Entomol. 47:175-205.
Shanovich, H.N. et al. 2019. Biology and Management of Japanese Beetle (Coleoptera: Scarabaeidae) in Corn and Soybean. J. Integ. Pest Mgmt. 10(1):9; 1-14. https://academic.oup.com/jipm/article/10/1/9/5454734
Shanovich, H.N., A.V. Ribeiro & R.L. Koch. 2021. Seasonal abundance, defoliation, and parasitism of Japanese beetle (Coleoptera: Scarabaeidae) in two apple cultivars. J. Econ. Entomol. 114: 811-817. https://doi.org/10.1093/jee/toaa315
Published August, 2024