Hostname: page-component-cd9895bd7-7cvxr Total loading time: 0 Render date: 2024-12-26T04:54:30.341Z Has data issue: false hasContentIssue false
  • English
  • Français

Transovarial effect of novaluron: persistence and residual effects on Stephanitis pyrioides (Hemiptera: Tingidae)

Published online by Cambridge University Press:  28 July 2021

Shimat V. Joseph Open the ORCID record for Shimat V. Joseph [Opens in a new window]
Shimat V. Joseph*
Affiliation:
Department of Entomology, University of Georgia, 1109 Experiment Street, Griffin, Georgia, 30223, United States of America
*
*Corresponding author. Email: [email protected]
Get access Rights & Permissions [Opens in a new window]

Abstract

Stephanitis pyrioides (Scott) (Hemiptera: Tingidae) is an important insect pest of azaleas, Rhododendron Linnaeus spp. (Ericaceae), in the United States of America. Because neonicotinoids, insecticides traditionally used against S. pyrioides, pose a risk to pollinators and natural enemies, nursery growers have reduced neonicotinoid use and are seeking alternative management options. Novaluron, an insect growth regulator, elicits a transovarial effect by reducing the viability of eggs after exposure to S. pyrioides adults. However, stability and persistence of transovarial effects on adults following exposure are not clear. The objectives of this study were to determine (1) the persistence of the transovarial effect of novaluron for up to three weeks after a single adult exposure and (2) the residual activity of aged novaluron residues eliciting a transovarial effect against S. pyrioides after a single application. Stephanitis pyrioides density was significantly lower in the novaluron-treated adults than in the nontreated controls for up to 21 days. The novaluron residues deposited on azalea foliage aged up to 32 days significantly reduced the number of S. pyrioides nymphs compared to that of the nontreated control. There was no significant difference in the number of nymphs among the 7-, 17-, and 32-day-old novaluron treatments relative to the nontreated control.

Type
Research Paper
Information
The Canadian Entomologist , Volume 153 , Issue 6 , December 2021 , pp. 702 - 713
Check for updates
Copyright
© The Author(s), 2021. Published by Cambridge University Press on behalf of the Entomological Society of Canada

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

Footnotes

Subject editor: David Siaussat

References

Alyokhin, A., Guillemette, R., and Choban, R. 2009. Stimulatory and suppressive effects of novaluron on the Colorado potato beetle reproduction. Journal of Economic Entomology, 102: 2078–2083.CrossRefGoogle ScholarPubMed
Alyokhin, A., Sewell, G., and Choban, R. 2008. Reduced viability of Colorado potato beetle, Leptinotarsa decemlineata, eggs exposed to novaluron. Pest Management Science, 64: 94–99.10.1002/ps.1459CrossRefGoogle ScholarPubMed
Braman, S.K., Pendley, A.F., Sparks, B., and Hudson, W.G. 1992. Thermal requirements for development, population trends, and parasitism of azalea lace bug (Heteroptera: Tingidae). Journal of Economic Entomology, 85: 870–877.10.1093/jee/85.3.870CrossRefGoogle Scholar
Bryden, J., Gill, R.J., Mitton, R.A.A., Raine, N.E., and Jansen, V.A.A. 2013. Chronic sublethal stress causes bee colony failure. Ecology Letters, 16: 1463–1469.CrossRefGoogle ScholarPubMed
Buntin, G.D., Braman, S.K., Gilbertz, D.A., and Phillips, D.V. 1996. Chlorosis, photosynthesis, and transpiration of azalea leaves after azalea lace bug (Heteroptera: Tingidae) feeding injury. Journal of Economic Entomology, 89: 990–995.CrossRefGoogle Scholar
Camacho, E.R. and Chong, J.H. 2015. General biology and current management approaches of soft scale pests (Hemiptera: Coccidae). Journal of Integrated Pest Management; 6: 17. https://doi.org./10.1093/jipm/pmv016.CrossRefGoogle Scholar
Chan, D.S.W. and Raine, R.E. 2021. Population decline in a ground-nesting solitary squash bee (Eucera pruinosa) following exposure to a neonicotinoid insecticide treated crop (Cucurbita pepo). Scientific Reports, 11: 4241. https://doi.org/10.1038/s41598-021-83341-7.CrossRefGoogle Scholar
Ciscoe, M. 2018. Azalea lace bugs are even peskier than the familiar rhododendron ones. Seattle Times. Available from https://www.seattletimes.com/pacific-nw-magazine/azalea-lace-bugs-are-even-peskier-than-the-familiar-rhododendron-ones/ [accessed on 1 March 2021].Google Scholar
Cowles, R.S. 2004. Impact of azadirachtin on vine weevil (Coleoptera: Curculionidae) reproduction. Agricultural and Forest Entomology, 6: 291–294.CrossRefGoogle Scholar
Cutler, G.C., Scott-Dupree, C.D., Tolman, J.H., and Harris, C.R. 2006. Toxicity of novaluron to the nontarget predatory bug, Podisus maculiventris (Heteroptera: Pentatomidae). Biological Control, 38: 196–204.CrossRefGoogle Scholar
Desmarchelier, J.M. and Allen, S.E. 1992. Diflubenzuron as a grain protectant for control of Sitophilus species. Journal of Stored Product Research, 28: 283–287.10.1016/0022-474X(92)90010-NCrossRefGoogle Scholar
Dutcher, J.D. 2007. General concepts in integrated pest and disease management. In Integrated management of plants pests and diseases. A review of resurgence and replacement causing pest outbreaks in IPM. Volume 1. Edited by Ciancio, A. and Mukerji, K.G.. Pp. 27–43.Google Scholar
Frank, S.D. and Tooker, J.F. 2020. Opinion: neonicotinoids pose undocumented threats to food webs. Proceedings of the National Academy of Sciences, 117: 22609–22613. https://doi.org/10.1073/pnas.2017221117.CrossRefGoogle Scholar
Gill, R.J. and Raine, N.E. 2014. Chronic impairment of bumblebee natural foraging behaviour induced by sublethal pesticide exposure. Functional Ecology, 28: 1459–1471. https://doi.org/10.1111/1365-2435.12292.CrossRefGoogle Scholar
Gill, R.J., Ramos-Rodriguez, O., and Raine, N.E. 2012. Combined pesticide exposure severely affects individual- and colony-level traits in bees. Nature, 491: 105–108.10.1038/nature11585CrossRefGoogle ScholarPubMed
Gökçe, A., Kim, S.H., Wise, J.C., and Whalon, M.E. 2009. Reduced egg viability in codling moth Cydia pomonella (L.) (Lepidoptera: Tortricidae) following adult exposure to novaluron. Pest Management Science, 65: 229–234.CrossRefGoogle ScholarPubMed
Graf, J.F. 1993. The role of insect growth regulators in arthropod control. Parasitology Today, 9: 471–474.CrossRefGoogle ScholarPubMed
Held, D.W. and Parker, S. 2011. Efficacy of soil-applied neonicotinoid insecticides against the azalea lace bug, Stephanitis pyrioides, in the landscape. Florida Entomologist, 94: 599–607.CrossRefGoogle Scholar
Insecticide Resistance Action Committee. 2016. Available from http://www.irac-online.org/modes-of-action/ [accessed on 1 March 2021].Google Scholar
Joseph, S.V. 2017. Effects of insect growth regulators on Bagrada hilaris (Hemiptera: Pentatomidae). Journal of Economic Entomology, 110: 2471–2477.10.1093/jee/tox264CrossRefGoogle Scholar
Joseph, S.V. 2019a. Transovarial effects of insect growth regulators on Stephanitis pyrioides (Hemiptera: Tingidae). Pest Management Science, 75: 2182–2187. https://doi.org/10.1002/ps.5342.CrossRefGoogle Scholar
Joseph, S.V. 2019b. Influence of insect growth regulators on Stephanitis pyrioides (Hemiptera: Tingidae) eggs and young nymphs. Insects, 10: 189. https://doi.org/10.3390/insects10070189.CrossRefGoogle Scholar
Joseph, S.V. 2020a. Ingestion of novaluron elicits transovarial activity in Stephanitis pyrioides (Hemiptera: Tingidae). Insects, 11: 216. https://doi.org/10.3390/insects11040216.CrossRefGoogle Scholar
Joseph, S.V. 2020b. Repellent effects of insecticides on Stephanitis pyrioides (Hemiptera: Tingidae) under laboratory conditions. Crop Protection, 127: 104985. https://doi.org/10.1016/j.cropro.2019.104985.CrossRefGoogle Scholar
Kim, S.H.S., Vandervoort, C., Whalon, M.E., and Wise, J.C. 2014. Transovarial transmission of novaluron in Choristoneura rosaceana (Lepidoptera: Tortricidae). The Canadian Entomologist 146: 347–353.10.4039/tce.2013.78CrossRefGoogle Scholar
Klingeman, W.E., Braman, S.K., and Buntin, G.D. 2000. Evaluating grower, landscape manager, and consumer perceptions of azalea lace bug (Heteroptera: Tingidae) feeding injury. Journal of Economic Entomology, 93: 141–148.CrossRefGoogle ScholarPubMed
Kostyukovsky, M. and Trostanetsky, A. 2006. The effect of a new chitin synthesis inhibitor, novaluron, on various developmental stages of Tribolium castaneum (Herbst). Journal of Stored Products Research, 42: 136–148.10.1016/j.jspr.2004.12.003CrossRefGoogle Scholar
Lin, Q.-C., Chen, H., Babendreier, D., Zhang, J.-P., Zhang, F., Dai, X.-Y., et al. 2021. Improved control of Frankliniella occidentalis on greenhouse pepper through the integration of Orius sauteri and neonicotinoid insecticides. Journal Pest Science, 94: 101–109. https://doi.org/10.1007/s10340-020-01198-7.CrossRefGoogle Scholar
Mommaerts, V., Sterk, G., and Smagghe, G. 2006. Hazards and uptake of chitin synthesis inhibitors in bumblebees, Bombus terrestris . Pest Management Science, 62: 752–758.CrossRefGoogle Scholar
Nair, S. and Braman, S.K. 2012. A scientific review on the ecology and management of the azalea lace bug Stephanitis pyrioides (Scott) (Tingidae: Hemiptera). Journal of Entomological Science, 47: 247–263.10.18474/0749-8004-47.3.247CrossRefGoogle Scholar
SAS Institute. 2012. SAS, Version 9.4. SAS Institute Inc., Cary, North Carolina, United States of America.Google Scholar
Sol, R. 1985. Diflubenzuron (Dimilin 25WP) for the control of the vine weevil (Otiorhynchus sulcatus F. (Col. Curc.)). Mededelingen van de Faculteit Landbouwwetenschappen Rijksuniversiteit Gent, 50: 457–461.Google Scholar
Trostanetsky, A. and Kostyukovsky, M. 2008. Transovarial activity of the chitin synthesis inhibitor novaluron on egg hatch and subsequent development of larvae of Tribolium castaneum . Phytoparasitica, 36: 38–41.10.1007/BF02980746CrossRefGoogle Scholar