Hostname: page-component-848d4c4894-hfldf Total loading time: 0 Render date: 2024-05-09T05:43:03.664Z Has data issue: false hasContentIssue false
  • English
  • Français

Sublethal effects of imidacloprid on the fecundity, longevity, and enzyme activity of Sitobion avenae (Fabricius) and Rhopalosiphum padi (Linnaeus)

Published online by Cambridge University Press:  10 May 2016

Y.-H. Lu ,
X.-S. Zheng  and
X.-W. Gao
Y.-H. Lu
Affiliation:
Institute of Plant Protection and Microbiology, Zhejiang Academy of Agricultural Sciences, Hangzhou 310021, China Department of Entomology, China Agricultural University, Beijing 100193, China
X.-S. Zheng
Affiliation:
Institute of Plant Protection and Microbiology, Zhejiang Academy of Agricultural Sciences, Hangzhou 310021, China
X.-W. Gao*
Affiliation:
Department of Entomology, China Agricultural University, Beijing 100193, China
*
*Author for correspondence Phone: +86-10-62732974 Fax: +86-10-62732974 E-mail: gaoxiwu@263.net.cn
Get access Rights & Permissions [Opens in a new window]

Abstract

The aphid species Sitobion avenae and Rhopalosiphum padi are the most important pests in wheat growing regions of many countries. In this study, we investigated the sublethal effects of imidacloprid on fecundity, longevity, and enzyme activity in both aphid species by comparing 3-h exposure for one or three generations. Our results indicated that 3-h exposure to sublethal doses of imidacloprid for one generation had no discernible effect on the survival, fecundity, longevity, or enzyme activity levels of aphids. However, when pulse exposures to imidacloprid were sustained over three generations, both fecundity and longevity were significantly decreased in both S. avenae and R. padi. Interestingly, the fecundity of R. padi had almost recovered by the F5 generation, but its longevity was still deleteriously affected. These results indicated that R. padi laid eggs in shorter time lags and has a more fast resilience. The change in reproduction behavior may be a phenomenon of R. padi to compensate its early death. If this is stable for the next generation, it means that the next generation is more competitive than unexposed populations, which could be the reason underlying population outbreaks that occur after longer-term exposure to an insecticide. This laboratory-based study highlights the sublethal effects of imidacloprid on the longevity and fecundity of descendants and provides an empirical basis from which to consider management decisions for chemical control in the field.

Keywords

imidaclopridaphidsurvivalfecunditysublethal effectsenzyme activity
Type
Research Papers
Information
Bulletin of Entomological Research , Volume 106 , Issue 4 , August 2016 , pp. 551 - 559
Check for updates
Copyright
Copyright © Cambridge University Press 2016 

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.)

References

Bayram, A., Salerno, G., Onofri, A. & Conti, E. (2010) Sub-lethal effects of two pyrethroids on biological parameters and behavioral responses to host cues in the egg parasitoid Telenomus busseolae . Biological Control 53, 153–160.CrossRefGoogle Scholar
Beers, E.H. & Himmel, P.D. (2002) Effect of chloronicotinyl insecticides on phytophagous and predatory mite populations in a cover spray program. in Proceedings of the 76th Annual Western Orchard Pest and Diseases Management Conference, 2002.Google Scholar
Biddinger, D. & Hull, L. (1999) Sublethal effects of selected insecticides on growth and reproduction of a laboratory susceptible strain of tufted apple bud moth (Lepidoptera: Tortricidae). Journal of Economic Entomology 92, 314–324.Google Scholar
Bradford, M.M. (1976) A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding. Analytical Biochemistry 72, 248–254.Google Scholar
Brown, R.A. (1989) Pesticides and non-target terrestrial invertebrates: an industrial approach. Pesticides and non-target invertebrates/editor: Paul C. Jepson.Google Scholar
Byrne, F.J., Castle, S., Prabhaker, N. & Toscano, N.C. (2003) Biochemical study of resistance to imidacloprid in B biotype Bemisia tabaci from Guatemala. Pest Management Science 59(3), 347–352 CrossRefGoogle Scholar
Christopher Cutler, G., Ramanaidu, K., Astatkie, T. & Isman, M.B. (2009) Green peach aphid, Myzus persicae (Hemiptera: Aphididae), reproduction during exposure to sublethal concentrations of imidacloprid and azadirachtin. Pest Management Science 65, 205–209.Google Scholar
Daniels, M., Bale, J.S., Newbury, H.J., Lind, R.J. & Pritchard, J. (2009) A sublethal dose of thiamethoxam causes a reduction in xylem feeding by the bird cherry-oat aphid (Rhopalosiphum padi), which is associated with dehydration and reduced performance. Journal of Insect Physiology 55, 758–765.CrossRefGoogle ScholarPubMed
Dastjerdi, H.R., Hejazi, M.J., Ganbalani, G.N. & Saber, M. (2009) Sublethal effects of some conventional and biorational insecticides on ectoparasitoid, Habrobracon hebetor Say (Hymenoptera: Braconidae). Journal of Entomology 6, 82–89.CrossRefGoogle Scholar
Desneux, N., Wajnberg, E., Fauvergue, X., Privet, S. & Kaiser, L. (2004 a) Sublethal effects of a neurotoxic insecticide on the oviposition behaviour and the patch-time allocation in two aphid parasitoids, Diaeretiella rapae and Aphidius matricariae. Entomologia Experimentalis et Applicata 112, 227–235.CrossRefGoogle Scholar
Desneux, N., Rafalimanana, H. & Kaiser, L. (2004 b) Dose–response relationship in lethal and behavioural effects of different insecticides on the parasitic wasp Aphidius ervi. Chemosphere 54, 619–627.CrossRefGoogle ScholarPubMed
Desneux, N., Decourtye, A. & Delpuech, J.M. (2007) The sublethal effects of pesticides on beneficial arthropods. Annual Review of Entomology 52, 81–106.CrossRefGoogle ScholarPubMed
Devonshire, A.L. & Moores, G.D. (1982) A carboxylesterase with broad substrate specificity causes organophosphorus, carbamate and pyrethroid resistance in peach-potato aphids (Myzus persicae). Pesticide Biochemistry and Physiology 18, 235–246.CrossRefGoogle Scholar
Drobne, D., Blažič, M., Van Gestel, C.A., Lešer, V., Zidar, P., Jemec, A. & Trebše, P. (2008) Toxicity of imidacloprid to the terrestrial isopod Porcellio scaber (Isopoda, Crustacea). Chemosphere 71, 1326–1334.CrossRefGoogle Scholar
Ellman, G.L., Courtney, K.D., Andres, V. & Featherstone, R.M. (1961) A new and rapid colorimetric determination of acetylcholinesterase activity. Biochemical Pharmacology 7, 88–95.CrossRefGoogle ScholarPubMed
Gao, S.J., Pang, B.P., Zhou, X.R. & Dong, Q.B. (2006) Seasonal dynamics of structure and diversity of insect communities in wheat fields. Chinese Bulletin of Entomology 3, 295–299.Google Scholar
Guo, L., Desneux, N., Sonoda, S., Liang, P., Han, P. & Gao, X.W. (2013) Sublethal and transgenerational effects of chlorantraniliprole on biological traits of the diamondback moth, Plutella xylostella L. Crop Protection 48, 29–34.CrossRefGoogle Scholar
Habig, W.H., Pabst, J. & Jackoby, W.B. (1974) Glutathione S-transferases. The first enzymatic step in mercapturic acid formation. Journal of Biological Chemistry 249, 7130–7139.CrossRefGoogle ScholarPubMed
Haynes, K.F. (1988) Sublethal effects of neurotoxic insecticides on insect behavior. Annual Review of Entomology 33, 149–168.CrossRefGoogle ScholarPubMed
He, Y.X., Zhao, J.W., Zheng, Y., Weng, Q.Y., Biondi, A., Desneux, N. & Wu, K.M. (2013) Assessment of potential sublethal effects of various insecticides on key biological traits of the tobacco whitefly, Bemisia tabaci . International Journal of Biological Sciences 9, 246–255.CrossRefGoogle ScholarPubMed
Jackson, A.E.M. & Wilkins, R.M. (1985) The effect of sub-lethal dosages of the synthetic pyrethroid fenvalerate on the reproductive rate of the aphid Myzus persicae . Pesticide Science 16, 364–368.Google Scholar
Joshi, N. & Sharma, V. (2009) Efficacy of imidacloprid (Confidor 200 SL) against aphids infesting wheat crop. Journal of Central European Agriculture 10, 217–222.Google Scholar
Lashkari, M.R., Sahragard, A. & Ghadamyari, M. (2007) Sublethal effects of imidacloprid and pymetrozine on population growth parameters of cabbage aphid, Brevicoryne brassicae on rapeseed, Brassica napus L. Insect Science 14, 207–212.CrossRefGoogle Scholar
Lowery, D.T., Sears, M.K., Lowery, D.T. & Sears, M.K. (1986) Stimulation of Reproduction of the Green Peach Aphid (Homoptera: Aphididae) by Azinphosmethyl Applied to Potatoes. Journal of Economic Entomology 79, 1530–1533(1534).Google Scholar
Lu, Y.H. & Gao, X.W. (2007) A method for mass culture of wheat aphids. Chinese Bulletin of Entomology 44, 289–290.Google Scholar
Lu, Y.H. & Gao, X.W. (2009) Multiple mechanisms responsible for differential susceptibilities of Sitobion avenae (Fabricius) and Rhopalosiphum padi (Linnaeus) to pirimicarb. Bulletin of Entomological Research 99, 611–617.Google Scholar
Lu, Y.H., He, Y.P. & Gao, X.W. (2013) Comparative studies on acetylcholinesterase characteristics between the aphids, Sitobion avenae and Rhopalosiphum padi . Journal of Insect Science 13, 9–16.CrossRefGoogle ScholarPubMed
Luckey, T.D. (1968) Insecticide Hormoligosis. Journal of Economic Entomology 61, 7–12.CrossRefGoogle ScholarPubMed
Metcalf, C.L., Flint, W.P. & Metcalf, R.L. (1962) Destructive and useful insects. Their habits and control. Destructive and useful insects. Their habits and control.Google Scholar
Miao, J., Du, Z.B., Wu, Y.Q., Gong, Z.J., Jiang, Y.L., Duan, Y., Li, T. & Lei, C.L. (2014) Sub-lethal effects of four neonicotinoid seed treatments on the demography and feeding behaviour of the wheat aphid Sitobion avenae . Pest Management Science 70, 55–59.CrossRefGoogle ScholarPubMed
Moharamipour, S., Monfared, A. & Fathipour, Y. (2003) Comparison of intrinsic rate of increase and mean relative growth rate of cabbage aphid (Brevicoryne brassicae L.) on four rapeseed (Brassica napus L.) varieties in a growth chamber. Agricultural Sciences 13, 79–86.Google Scholar
Moores, G.D., Gao, X., Denholm, I. & Devonshire, A.L. (1996) Characterisation of insensitive acetylcholinesterase in insecticide-resistant cotton aphids, aphis gossypiiGlover (Homoptera: Aphididae). Pesticide Biochemistry and Physiology 56, 102–110.CrossRefGoogle Scholar
Morse, J. & Zareh, N. (1991) Pesticide-induced hormoligosis of citrus thrips (Thysanoptera: Thripidae) fecundity. Journal of Economic Entomology 84, 1169–1174.CrossRefGoogle Scholar
Moser, S.E. & Obrycki, J.J. (2009) Non-target effects of neonicotinoid seed treatments; mortality of coccinellid larvae related to zoophytophagy. Biological Control 51, 487–492.CrossRefGoogle Scholar
Nauen, R., Koob, B. & Elbert, A. (2003) Antifeedant effects of sublethal dosages of imidacloprid on Bemisia tabaci . Entomologia Experimentalis Et Applicata 88, 287–293.CrossRefGoogle Scholar
Robson, J.D., MG, W. & RPP, A. (2010) Effect of imidacloprid foliar treatment and banana leaf age on Pentalonia nigronervosa (Hemiptera, Aphididae) survival. New Zealand Journal of Crop & Horticultural Science 35, 415–422.CrossRefGoogle Scholar
Shotkoski, F.A., Mayo, Z.B. & Peters, L.L. (1990) Induced disulfoton resistance in greenbugs (Homoptera: Aphididae). Journal of Economic Entomology 83, 2147–2152.CrossRefGoogle Scholar
Shufran, R.A., Wilde, G.E. & Sloderbeck, P.E. (1997) Response of three greenbug (Homoptera: Aphididae) strains to five organophosphorous and two carbamate insecticides. Journal of Economic Entomology 90, 283–286.CrossRefGoogle Scholar
Sohrabi, F., Shishehbor, P., Saber, M. & Mosaddegh, M.S. (2011) Lethal and sublethal effects of buprofezin and imidacloprid on Bemisia tabaci (Hemiptera: Aleyrodidae). Crop Protection 30, 1190–1195.CrossRefGoogle Scholar
Sohrabi, F., Saber, M., Shishehbor, P. & Mosaddegh, M.S. (2012) Lethal and sublethal effects of buprofezin and imidacloprid on the whitefly parasitoid Encarsia inaron (Hymenoptera: Aphelinidae). Crop Protection 32, 83–89.CrossRefGoogle Scholar
Van Asperen, K. (1962) A study of housefly esterases by means of a sensitive colorimetric method. Journal of Insect Physiology 8, 401–416.CrossRefGoogle Scholar
Wang, X.Y., Yang, Z.Q., Shen, Z.R., Lu, J. & Xu, W.B. (2008) Sublethal effects of selected insecticides on fecundity and wing dimorphism of green peach aphid (Hom., Aphididae). Journal of Applied Entomology 132, 135–142.CrossRefGoogle Scholar
Xing, J., Liang, P. & Gao, X.W. (2011) Effects of sublethal concentrations of chlorantraniliprole on insecticide susceptibility and detoxifying enzyme activity in Plutella xylostella . Chinese Journal of Pesticide Science 13, 464–470.Google Scholar