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Environment polluting conventional chemical control compared to an environmentally friendly IPM approach for control of diamondback moth, Plutella xylostella (L.), in China: a review

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Abstract

The diamondback moth, Plutella xylostella, is recognized as a widely distributed destructive insect pest of Brassica worldwide. The management of this pest is a serious issue, and an estimated annual cost of its management has reached approximately US$4 billion. Despite the fact that chemicals are a serious threat to the environment, lots of chemicals are applied for controlling various insect pests especially P. xylostella. An overreliance on chemical control has not only led to the evolution of resistance to insecticides and to a reduction of natural enemies but also has polluted various components of water, air, and soil ecosystem. In the present scenario, there is a need to implement an environmentally friendly integrated pest management (IPM) approach with new management tactics (microbial control, biological control, cultural control, mating disruption, insecticide rotation strategies, and plant resistance) for an alternative to chemical control. The IPM approach is not only economically beneficial but also reduces the environmental and health risks. The present review synthesizes published information on the insecticide resistance against P. xylostella and emphasizes on adopting an alternative environmentally friendly IPM approach for controlling P. xylostella in China.

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References

  • Alizadeh M, Rassoulian G, Karimzadeh J, Hosseini-Naveh V, Farazmand H (2011) Biological study of Plutella xylostella (L.)(Lep: Plutellidae) and it’s solitary endoparasitoid, Cotesia vestalis (Haliday)(Hym. Braconidae) under laboratory conditions. Pak J Biol Sci 14:1090–1099

    CAS  Google Scholar 

  • Altmann J (1988) An investigation of resistance in cabbage moth (Plutella xylostella L.) to pyrethroids in the Lockyer Valley. Graduate Diploma Thesis, Queensland Agricultural College, Lawes, Qld

  • Alvi MS, Momoi S (1994) Environmental regulation and geographical adaptation of diapause in Cotesia plutellae (Hymenoptera: Braconidae), a parasitoid of the diamondback moth larvae. Appl Entomol Zool 29:89–95

    Google Scholar 

  • Ankersmit G (1953) DDT-resistance in Plutella maculipennis (Curt.)(Lep.) in Java. Bull Entomol Res 44:421–425

    CAS  Google Scholar 

  • Ayra-Pardo C, Raymond B, Gulzar A, Rodríguez-Cabrera L, Morán-Bertot I, Crickmore N, Wright DJ (2015) Novel genetic factors involved in resistance to Bacillus thuringiensis in Plutella xylostella. Insect Mol Biol 24:589–600

    CAS  Google Scholar 

  • Badenes-Perez FR, Shelton AM, Nault BA (2004) Evaluating trap crops for diamondback moth, Plutella xylostella (Lepidoptera: Plutellidae). J Econ Entomol 97:1365–1372

    Google Scholar 

  • Baker TC (2008) Use of pheromones in IPM. In: Radcliffe EB, Hutchison WD, Cancelado RE (eds) Integrated pest management. Cambridge University Press, Cambridge, MA, pp 273–285

    Google Scholar 

  • Barriuso E, Koskinen W (1996) Incorporating nonextractable atrazine residues into soil size fractions as a function of time. Soil Sci Soc Am J 60:150–157

    CAS  Google Scholar 

  • Barroga S, Morallo-Rejesus B (1974) A survey of diamondback moth population for resistance to the insecticides in the Philippines. MS thesis. Univ. Philippines at Los Banos, Philippines

  • Black BC, Hollingworth RM, Ahammadsahib KI, Kukel CD, Donovan S (1994) Insecticidal action and mitochondrial uncoupling activity of AC-303,630 and related halogenated pyrroles. Pestic Biochem Physiol 50:115–128

    CAS  Google Scholar 

  • Buckingham S, Hosie A, Roush R, Sattelle D (1994) Actions of agonists and convulsant antagonists on a Drosophila melanogaster GABA receptor (Rdl) homo-oligomer expressed in Xenopus oocytes. Neurosci Lett 181:137–140

    CAS  Google Scholar 

  • Chai B, He X, Wang J, Li Z, Liu C (2010) Synthesis of cyantraniliprole and its bioactivity. Agrochemicals 49:167–169

    CAS  Google Scholar 

  • Chandramohan N (1994) Seasonal incidence of diamondback moth, Plutella xylostella L. and its parasitoids in Nilgiris. J Biol contr 8:77–80

    Google Scholar 

  • Charleston DS, Kfir R (2000) The possibility of using Indian mustard, Brassica juncea, as a trap crop for the diamondback moth, Plutella xylostella, in South Africa. Crop Prot 19:455–460

    Google Scholar 

  • Chauhan U, Sharma K, Kirk A, Bordat D (2002) Status of biocontrol agents of Plutella xylostella (L.)(Lepidoptera: Yponomeutidae) in hilly areas of the north-west Himalayas, India. In: Improving biocontrol of Plutella xylostella. Proceedings of the International Symposium, 21Á/24 October, p 153Á

  • Chen L, Kuang M, Zhen Z, Cao Y, Xu W (1987) A survey of natural enemies of insect pests of vegetable crops in the suburbs of Guangzhou. In: al FH-Ze (ed) Integrated control of insect pests and diseases in vegetable crops. pp 393–399

  • Chen HY, Zhang DY, Huang H, Li ZY, Hu ZD, Feng X (2010) Insecticidal activities and field efficacy of Chlorantraniliprole against diamondback moth (Plutella xylostella). Guangdong Agric Sci 2:96–98

    Google Scholar 

  • Chou YH, Lin YM, Hsu CL (1977) Sex pheromone of the diamondback moth (Lepidoptera: Plutellidae). Bull Inst Zool Acad Sin 16:99–105

    Google Scholar 

  • Cole LM, Nicholson RA, Casida JE (1993) Action of phenylpyrazole insecticides at the GABA-gated chloride channel. Pestic Biochem Physiol 46:47–54

    CAS  Google Scholar 

  • Cordova D et al (2006) Anthranilic diamides: a new class of insecticides with a novel mode of action, ryanodine receptor activation. Pestic Biochem Physiol 84:196–214

    CAS  Google Scholar 

  • Cully DF, Paress PS, Liu KK, Schaeffer JM, Arena JP (1996) Identification of a Drosophila melanogaster glutamate-gated chloride channel sensitive to the antiparasitic agent avermectin. J Biol Chem 271:20187–20191

    CAS  Google Scholar 

  • Delvare G, Kirk A, Bordet D (2004) The taxonomic status and role of Hymenoptera in biological control of DBM, Plutella xylostella (L.)(Lepidoptera: Plutellidae). In: Improving biocontrol of Plutella xylostella. CIRAD, Montpellier, pp 17–49

    Google Scholar 

  • Diez M, Gallardo F, Tortella G, Rubilar O, Navia R, Bornhardt C (2012) Chlorophenol degradation in soil columns inoculated with Anthracophyllum discolor immobilized on wheat grains. J Environ Manag 95:S83–S87

    CAS  Google Scholar 

  • Ebbinghaus-Kintscher U et al (2006) Phthalic acid diamides activate ryanodine-sensitive Ca 2+ release channels in insects. Cell Calcium 39:21–33

    CAS  Google Scholar 

  • FAO (2012) Production Statistics: Rome: FAO.http://faostat.fao.org/site/567/default.aspx#.

  • Feng Q, Liu ZL, Xiong LX, Wang MZ, Li YQ, Li ZM (2010) Synthesis and insecticidal activities of novel anthranilic diamides containing modified N-pyridylpyrazoles. J Agric Food Chem 58:12327–12336

    CAS  Google Scholar 

  • Feng X et al (2011) Research progress of the resistance management and sustainable control of diamondback moth (Plutella xylostella) in China. Chin J Appl Entomol 48:247–253

    Google Scholar 

  • Furlong MJ, Zalucki MP (2007) Parasitoid complex of diamondback moth in south east Queensland: first records of Oomyzus sokolowskii (Hymenoptera: Eulophidae) in Australia. Aust J Entomol 46:167–175

    Google Scholar 

  • Furlong MJ, Shi Z, Liu SS, Zalucki MP (2004) Evaluation of the impact of natural enemies on Plutella xylostella L.(Lepidoptera: Yponomeutidae) populations on commercial Brassica farms. Agric Forest Entomol 6:311–322

    Google Scholar 

  • Furlong MJ, Ju KH, Su PW, Chol JK, Il RC, Zalucki MP (2008) Integration of endemic natural enemies and Bacillus thuringiensis to manage insect pests of Brassica crops in North Korea. Agric, Ecosys & Environ 125:223–238

    Google Scholar 

  • Furlong MJ, Wright DJ, Dosdall LM (2013) Diamondback moth ecology and management: problems, progress, and prospects. Annu Rev Entomol 58:517–541

    CAS  Google Scholar 

  • Goulet H, Huber JT (1993) Hymenoptera of the world: an identification guide to families. Centre for land and biological resources. Ontario, USA

    Google Scholar 

  • Guo M, Zhu D, Li L (1999) Selection of Trichogramma species for controlling the diamondback moth Plutella xylostella (L.) Ins Sci 6:187–192

    Google Scholar 

  • Guo L, Wang Y, Zhou X, Li Z, Liu S, Pei L, Gao X (2014) Functional analysis of a point mutation in the ryanodine receptor of Plutella xylostella (L.) associated with resistance to chlorantraniliprole. Pest Manag Sci 70:1083–1089

    CAS  Google Scholar 

  • Hama H, Suzuki K, Tanaka H (1992) Inheritance and stability of resistance to Bacillus thuringiensis formulations of the diamondback moth, Plutella xylostella (Linnaeus)(Lepidoptera: Yponomeutidae). Appl Entomol Zool 27:355–362

    Google Scholar 

  • Harcourt D (1957) Biology of the diamondback moth, Plutella maculipennis (Curt.)(Lepidoptera: Plutellidae), in eastern Ontario. II. Life-history, behaviour, and host relationships. Can Entomol 89:554–564

    Google Scholar 

  • Hardy JE (1938) Plutella maculipennis, Curt., its natural and biological control in England. Bull Entomol Res 29:343–372

    Google Scholar 

  • He YR, Chen KW, Pang XF (2002) Egg parasitoids of Plutella xylostella in South China. In: Improving biocontrol of Plutella xylostella. CIRAD/USDA/INRA Laboratories, pp. 267

  • Hirooka T, Nishimatsu T, Kodama H, Reckmann U, Nauen R (2007) The biological profile of flubendiamide, a new benzenedicarboxamide insecticide. Pflanzenschutz Nachrichten-Bayer-English Edition 60:183

    CAS  Google Scholar 

  • Hou Y, Pang X, Liang G, YOU M (2001) Control effect of Plutella xylostella with synthetic sex pheromone. Chin J Biol Contr 17:121–125

    Google Scholar 

  • Hu Z, Feng X, Li Z, Zhang D, Chen H (2010) Studies on the susceptibility of diamondback moth (DBM), Plutella xylostella L., to chlorantraniliprole in different vegetable fields [J]. Agrochem Res Appl 3:008

  • Huang S, Chen K, Shen S (2002) Natural increase of parasitoids population of diamondback moth Plutella xylostella under ecological control condition. J Appl Ecol 13:1449–1451

    Google Scholar 

  • Huang F, Cao TT, Shi M, Chen YF, Xx C (2008) Parasitism-induced effects on host growth and metabolic efficiency in Plutella xylostella larvae parasitized by Cotesia vestalis or Diadegma semiclausum. Ins Sci 15:237–243

    Google Scholar 

  • Huang B, Shi Z, Hou Y (2014) Host selection behavior and the fecundity of Plutella xylostella (Lepidoptera: Plutellidae) on multiple host plants. J Ins Sci 14:251

  • Hussain S, Sørensen SR, Devers-Lamrani M, El-Sebai T, Martin-Laurent F (2009) Characterization of an isoproturon mineralizing bacterial culture enriched from a French agricultural soil. Chemosphere 77:1052–1059

    CAS  Google Scholar 

  • Ishaaya I (1993) Insect detoxifying enzymes: their importance in pesticide synergism and resistance. Arch Ins Biochem Physiol 22:263–276

    CAS  Google Scholar 

  • Ishaaya I, Kontsedalov S, Mazirov D, Horowitz AR (2001) Biorational agents—mechanism and importance in IPM and IRM programs for controlling agricultural pests. In: Proceedings of the 53rd International Symposium on Crop Protection, Vol 66, Meded. Fac. Landbouww., Univ. Gent, vol 2a. pp 363–374

  • Jiang T, Wu S, Yang T, Zhu C, Gao C (2015) Monitoring field populations of Plutella xylostella (Lepidoptera: Plutellidae) for resistance to eight insecticides in China. Flor Entomol 98:65–73

    CAS  Google Scholar 

  • Justus KA, Dosdall LM, Mitchell BK (2000) Oviposition by Plutella xylostella (Lepidoptera: Plutellidae) and effects of phylloplane waxiness. J Econ Entomol 93:1152–1159

    CAS  Google Scholar 

  • Kamble S, Hadapad AB, Eapen S (2013) Evaluation of transgenic lines of Indian mustard (Brassica juncea L. Czern and Coss) expressing synthetic cry1Ac gene for resistance to Plutella xylostella. J Plant Biotech 115:321–328

    CAS  Google Scholar 

  • Kang Z-J, Gong Y-J, Zhu L, Lu H, Shi B-C (2011) Trapping efficiency on Plutella xylostella among three type of sex pheromone lures. Chin J Northern Hortic 6:059

    Google Scholar 

  • Kato M, Itioka T, Sakai S, Momose K, Yamane S, Hamid AA, Inoue T (2000) Various population fluctuation patterns of light-attracted beetles in a tropical lowland dipterocarp forest in Sarawak. Popul Ecol 42:97–104

    Google Scholar 

  • Ke L, Fang J (1982) Studies on the biology of the braconid wasp, Apanteles plutellae Kurdjumov. Act Phyto Sin 9:27–34

    Google Scholar 

  • Kfir R (1998) Origin of the diamondback moth (Lepidoptera: Plutellidae). Ann Entomol Soc Amer 91:164–167

    Google Scholar 

  • Koshihara T, Yamada H (1980) Attractant activity of the female sex pheromone of diamondback moth, Plutella xylostella (L.), and analogue. Jap J Appl Entomol Zool 24:6–12

    CAS  Google Scholar 

  • Kumar H (2004) Orientation, feeding, and ovipositional behavior of diamondback moth, Plutella xylostella (Lepidoptera: Plutellidae), on transgenic cabbage expressing Cry1Ab toxin of Bacillus thuringiensis (Berliner). Environ Entomol 33:1025–1031

    CAS  Google Scholar 

  • Kuwahara M, Keinmeesuke P, Sinchaisri N (1995) Present status of resistance of the diamondback moth, Plutella xylostella L., to insecticides in Thailand. Appl Entomol Zool 30:557–566

    CAS  Google Scholar 

  • Lasota JA, Dybas RA (1991) Avermectins, a novel class of compounds: implications for use in arthropod pest control. Annu Rev Entomol 36:91–117

    CAS  Google Scholar 

  • Li J, Wu J, Yu Z, Akhurst R (1997) Resistance of Plutella xylostella (L.) to Bacillus thuringiensis. J Huazhong Agric Uni 17:214–217

    Google Scholar 

  • Li Z, Feng X, Liu S-S, You M, Furlong MJ (2016) Biology, ecology, and management of the diamondback moth in China. Annu Rev Entomol 61:277–296

    CAS  Google Scholar 

  • Liang P, Gao X, Zheng B, Dai H (2001) Study on resistance mechanism and cross-resistance of abamectin in diamondback moth Plutella xylostella (L.) Chin J Pestic Sci 3:41–45

    CAS  Google Scholar 

  • Lim G-S (1986a) Biological control of diamondback moth. Talekar, NS & Griggs, TD:159

  • Lim GS (1986b) Biological control of diamondback moth, and Other Crucifer Pests. In: Talekar NS, Griggs TD (eds) The biology and effects of parasites on the diamond-back moth, Plutella xylostella (L.), Tainan, Taiwan

  • Liu S-S, Jiang L-H (2003) Differential parasitism of Plutella xylostella (Lepidoptera: Plutellidae) larvae by the parasitoid Cotesia plutellae (Hymenoptera: Braconidae) on two host plant species. Bull Entomol Res 93:65–72

    Google Scholar 

  • Liu S, Yan S (1998) Brassica IPM in Asia: successes, challenges, and opportunities. Pest Manag Fut Chal:85–97

  • Liu S-S, Wang X-G, Guo S-J, He J-H, Shi Z-H (2000) Seasonal abundance of the parasitoid complex associated with the diamondback moth, Plutella xylostella (Lepidoptera: Plutellidae) in Hangzhou, China. Bull Entomol Res 90:221–231

    CAS  Google Scholar 

  • Liu Y-H, Chung Y-C, Xiong Y (2001) Purification and characterization of a dimethoate-degrading enzyme of Aspergillus niger ZHY256, isolated from sewage. Appl Environ Microbiol 67:3746–3749

    CAS  Google Scholar 

  • Liu S-S, Chen F-Z, Zalucki MP (2002) Development and survival of the diamondback moth (Lepidoptera: Plutellidae) at constant and alternating temperatures. Environ Entomol 31:221–231

    Google Scholar 

  • Liu X, Ning Y, Wang H, Wang K (2015) Cross-resistance, mode of inheritance, synergism, and fitness effects of cyantraniliprole resistance in Plutella xylostella. Entomol Exp Appl 157:271–278

    CAS  Google Scholar 

  • Löhr B, Gichini G, Roßbach A, Nyambo B (2006) After release dispersal of Diadegma semiclausum and its effect on diamondback moth population, damage and indigenous parasitoids. In: Proceedings of the 5th International Workshop on Diamondback Moth and Other Crucifer Insect Pests. , Beijing, China, pp 24–27

  • Lu Y-X (1983) A preliminary survey of natural enemies of larvae of Plutella xylostella. Nat Enem of Ins 5:188–189

    Google Scholar 

  • Lu J-H, Liu S-S, Shelton A (2004) Laboratory evaluations of a wild crucifer Barbarea vulgaris as a management tool for the diamondback moth Plutella xylostella (Lepidoptera: Plutellidae). Bull Entomol Res 94:509–516

    Google Scholar 

  • Lund AE, Narahashi T (1983) Kinetics of sodium channel modification as the basis for the variation in the nerve membrane effects of pyrethroids and DDT analogs. Pestic Biochem Physiol 20:203–216

    CAS  Google Scholar 

  • Ma J, Li D, Keller M, Schmidt O, Feng X (2005) A DNA marker to identify predation of Plutella xylostella (Lep., Plutellidae) by Nabis kinbergii (Hem., Nabidae) and Lycosa sp.(Aranaea, Lycosidae). J Appl Entomol 129:330–335

    CAS  Google Scholar 

  • Moffat AS (1993) New chemicals seek to outwit insect pests. Science 261:550–551

    CAS  Google Scholar 

  • Munir S, Dosdall LM, O’Donovan JT (2015) Evolutionary ecology of diamondback moth, Plutella xylostella (L.) and Diadegma insulare (Cresson) in North America: a review. Ann Res Rev Biol 5:189

    Google Scholar 

  • Nauen R (2006) Insecticide mode of action: return of the ryanodine receptor. Pest Manag Sci 62:690–692

    CAS  Google Scholar 

  • Nemoto H, Yano E, Kiritani K Pheromonal control of diamondback moth in the management of crucifer pests. In: Proceedings of the Second International Workshop on Diamondback Moth and Other Cruciferous Pests, Tainan, Taiwan, 1992. AVRDC, pp 91–97

  • Niu YQ, Sun YX, Liu TX (2014) Development and reproductive potential of diamondback moth (Lepidoptera: Plutellidae) on selected wild crucifer species. Environ Entomol 43:69–74

    Google Scholar 

  • Ohbayashi N, Shimizu K, Nagata K Control of diamondback moth using synthetic sex pheromones. In: The Management of Diamondback Moth and Other Crucifer Pests Proceedings of the 2nd International Workshop, 1990. pp 10–14

  • Ooi PA (1992) Role of parasitoids in managing diamondback moth in the Cameron Highlands, Malaysia, diamondback moth and other crucifer pests:255–262

  • Philips C, Fu Z, Kuhar T, Shelton A, Cordero R (2014) Natural history, ecology, and management of diamondback moth (Lepidoptera: Plutellidae), with emphasis on the United States. J Integ Pest Manag 5:D1–D11

    Google Scholar 

  • Pimprale SS, Besco CL, Bryson PK, Brown TM (1997) Increased susceptibility of pyrethroid-resistant tobacco budworm (Lepidoptera: Noctuidae) to chlorfenapyr. J Econ Entomol 90:49–54

    CAS  Google Scholar 

  • Prasad Y, Prabhakar M (2012) Pest monitoring and forecasting. In: Shankar U, Abrol DP (eds) Integrated pest management: principles and practice. Oxfordshire, United Kingdom, pp 41–57

    Google Scholar 

  • Pu X, Yang Y, Wu S, Wu Y (2010) Characterisation of abamectin resistance in a field-evolved multiresistant population of Plutella xylostella. Pest Manag Sci 66:371–378

    CAS  Google Scholar 

  • Qian L, Cao G, Song J, Yin Q, Han Z (2008) Biochemical mechanisms conferring cross-resistance between tebufenozide and abamectin in Plutella xylostella. Pestic Biochem Physiol 91:175–179

    CAS  Google Scholar 

  • Raimondo S, Strazanac JS, Butler L (2004) Comparison of sampling techniques used in studying Lepidoptera population dynamics. Environ Entomol 33:418–425

    Google Scholar 

  • Ramachandran S, Buntin GD, All JN, Raymer PL, Stewart CN (1998) Greenhouse and field evaluations of transgenic canola against diamondback moth, Plutella xylostella, and corn earworm, Helicoverpa zea. Entomol Exp Appl 88:17–24

    Google Scholar 

  • Rosell G, Quero C, Coll J, Guerrero A (2008) Biorational insecticides in pest management. J Pestic Sci 33:103–121

    CAS  Google Scholar 

  • Rubilar O, Feijoo G, Diez C, Lu-Chau T, Moreira M, Lema J (2007) Biodegradation of pentachlorophenol in soil slurry cultures by Bjerkandera adusta and Anthracophyllum discolor. Ind Eng Chem Res 46:6744–6751

    CAS  Google Scholar 

  • Ruder FJ, Kayser H (1992) The carbodiimide product of diafenthiuron reacts covalently with two mitochondrial proteins, the F0-proteolipid and porin, and inhibits mitochondrial ATPase in vitro. Pestic Biochem Physiol 42:248–261

    CAS  Google Scholar 

  • Saito T et al. (1990) Challenge to diamondback moth resistance to insecticides. In: International Conference on Plant Protection in the Tropics, Genting Highlands, Pahang (Malaysia), 20–23 Mar 1990. Malaysian Plant Protection Society

  • Sammour E, Kandil M, Abdel-Aziz W (2008) The reproductive potential and fate of chlorfluazuron and leufenuron against cotton leafworm Spodoptera littoralis (Boisd.) Am Eurasian J Agric Environ Sci 4:62–67

    Google Scholar 

  • Sarfraz M, Keddie AB, Dosdall LM (2005) Biological control of the diamondback moth, Plutella xylostella: a review. Biocont Sci Tech 15:763–789

    Google Scholar 

  • Satpathy S, Shivalingaswamy T, Kumar A, Rai A, Rai M (2010) Potentiality of Chinese cabbage (Brassica rapa subsp. pekinensis) as a trap crop for diamondback moth (Plutella xylostella) management in cabbage. Ind J Agric Sci 80:238–241

    Google Scholar 

  • Sattelle DB, Cordova D, Cheek TR (2008) Insect ryanodine receptors: molecular targets for novel pest control chemicals. Invertebr Neurosci 8:107–119

    CAS  Google Scholar 

  • Saucke H, Dori F, Schmutterer H (2000) Biological and integrated control of Plutella xylostella (Lep., Yponomeutidae) and Crocidolomia pavonana (Lep., Pyralidae) in brassica crops in Papua New Guinea. Biocont Sci Tech 10:595–606

    Google Scholar 

  • Schnepf E et al (1998) Bacillus thuringiensis and its pesticidal crystal proteins. Microbiol Mol Biol Rev 62:775–806

    CAS  Google Scholar 

  • Shang JY, Shao YM, Lang GJ, Yuan G, Tang ZH, Zhang CX (2007) Expression of two types of acetylcholinesterase gene from the silkworm, Bombyx mori, in insect cells. Ins Sci 14:443–449

    CAS  Google Scholar 

  • Sharov AA, Thorpe KW, Tcheslavskaia K (2002) Effect of synthetic pheromone on gypsy moth (Lepidoptera: Lymantriidae) trap catch and mating success beyond treated areas. Environ Entomol 31:1119–1127

    CAS  Google Scholar 

  • Shelton MA (2004) Management of the diamondback moth: deja vu all over again? In: Endersby NM, Ridland PM (eds) The management of diamondback moth and other crucifer pests. Department of Natural Resources and Environment, Melbourne, pp 3–8

    Google Scholar 

  • Shelton A, Wyman J, Cushing N, Apfelbeck K, Dennehy T, Mahr S, Eigenbrode S (1993) Insecticide resistance of diamondback moth (Lepidoptera: Plutellidae) in North America. J Eco Entomol 86:11–19

    CAS  Google Scholar 

  • Shelton A, Perez C, Tang J, Vandenberg J (1997) Prospects for novel approaches towards management of the diamondback moth. The management of diamondback moth and other crucifer pests:17–20

  • Sheppard CD, Joyce JA (1998) Increased susceptibility of pyrethroid-resistant horn flies (Diptera: Muscidae) to chlorfenapyr. J Econ Entomol 91:398–400

    CAS  Google Scholar 

  • Shi Z-H, Liu S-S, Li Y-X (2002) Cotesia plutellae parasitizing Plutella xylostella: host-age dependent parasitism and its effect on host development and food consumption. BioControl 47:499–511

    Google Scholar 

  • Soderlund D, Knipple D (2003) The molecular biology of knockdown resistance to pyrethroid insecticides. Ins Biochem Mol Biol 33:563–577

    CAS  Google Scholar 

  • Sparks TC, Dripps JE, Watson GB, Paroonagian D (2012) Resistance and cross-resistance to the spinosyns—a review and analysis. Pestic Biochem Physiol 102:1–10

    CAS  Google Scholar 

  • Sun J, Liang P, Gao X (2012) Cross resistance patterns and fitness in fufenozide resistant diamondback moth, Plutella xylostella (Lepidoptera: Plutellidae). Pest Manag Sci 68:285–289

    CAS  Google Scholar 

  • Sutherland T, Weir K, Lacey M, Horne I, Russell R, Oakeshott J (2002) Enrichment of a microbial culture capable of degrading endosulphate, the toxic metabolite of endosulfan. J Appl Microbiol 92:541–548

    CAS  Google Scholar 

  • Syed A (1992) Insecticide resistance in diamondback moth in Malaysia. Diamondback moth and other crucifer pests:437–442

  • Symondson W, Sunderland K, Greenstone M (2002) Can generalist predators be effective biocontrol agents? 1. Annu Rev Entomol 47:561–594

    CAS  Google Scholar 

  • Tabashnik BE, Cushing NL, Johnson MW (1987) Diamondback moth (Lepidoptera: Plutellidae) resistance to insecticides in Hawaii: intra-island variation and cross-resistance. J Eco Entomol 80:1091–1099

    CAS  Google Scholar 

  • Tabashnik BE, Cushing NL, Finson N, Johnson MW (1990) Field development of resistance to Bacillus thuringiensis in diamondback moth (Lepidoptera: Plutellidae). J Econ Entomol 83:1671–1676

    Google Scholar 

  • Talekar N (2004) Biological control of diamondback moth in Asia. Improving biocontrol of Plutella xylostella. CIRAD Montpellier, France

    Google Scholar 

  • Talekar N, Shelton A (1993) Biology, ecology, and management of the diamondback moth. Annu Rev Entomol 38:275–301

    Google Scholar 

  • Talekar N, Yang J, Lee S (1992) Introduction of Diadegma semiclausum to control diamondback moth in Taiwan. In: Diamondback moth and other crucifer pests: Proceedings of the Second International Workshop, Tainan, Taiwan. Taipei: Asian Vegetable Research and Development Center, c1992

  • Talekar NS, Liu S-H, Chen C-L, Yiin Y-F (1994) Characteristics of oviposition of diamondback moth (Lepidoptera: Yponomeutidae) on cabbage. Zool Stu 33:72–77

    Google Scholar 

  • Tamaki Y et al (1977) (Z)-11-Hexadecenal and (Z)-11-hexadecenyl acetate: sex-pheromone components of the diamondback moth (Lepidoptera: Plutellidae). Appl Entomol Zool 12:208–210

    CAS  Google Scholar 

  • Tang W, Yu L, He W, Yang G, Ke F, Baxter SW, You S, Douglas CJ, You M (2014) DBM-DB: the diamondback moth genome database. Database 2014, pp bat087. doi:10.1093/database/bat087

    Google Scholar 

  • Thompson GD, Dutton R, Sparks TC (2000) Spinosad—a case study: an example from a natural products discovery programme. Pest Manag Sci 56:696–702

    CAS  Google Scholar 

  • Tohnishi M et al (2005) Flubendiamide, a novel insecticide highly active against lepidopterous insect pests. J Pestic Sci 30:354–360

    CAS  Google Scholar 

  • Tomlin C (2000) The pesticide manual, 12th edn. BCPC, Farnham

    Google Scholar 

  • Ventura OD (1997) Experiences with biological control of diamondback moth in the Philippines. In: The management of diamondback moth and other crucifer pests. Proceedings of the Third International Workshop. Malaysian Agricultural Research and Development Institute (MARDI), Kuala Lumpur, pp 67–70

  • Verkerk RH, Wright DJ (1996) Multitrophic interactions and management of the diamondback moth: a review. Bull Entomol Res 86:205–216

    Google Scholar 

  • Vickers R, Furlong M, White A, Pell J (2004) Initiation of fungal epizootics in diamondback moth populations within a large field cage: proof of concept for auto dissemination. Entomol Exper Applic 111:7–17

    Google Scholar 

  • Vos HCCAA (1953) Introduction in Indonesia of Angitia cerophaga Grav., a parasitoid of Plutella maculipennis Curt. Contribution of Central Agricultural Research Station:1–32

  • Wang X-G, Liu S-S (2002) Effects of host age on the performance of Diadromus collaris, a pupal parasitoid of Plutella xylostella. BioControl 47:293–307

    Google Scholar 

  • Wang X, Wu Y (2012) High levels of resistance to chlorantraniliprole evolved in field populations of Plutella xylostella. J Econ Entomol 105:1019–1023

    CAS  Google Scholar 

  • Wang C, Wu S, Yang Y, Wu Y (2005) Field--evolved resistance to Bt delta endotoxins and Bt formulation in {Plutella xylostella} from the southeastern coast region of China. Acta Entomol Sin 49:70–73

    Google Scholar 

  • Wang X, Li X, Shen A, Wu Y (2010) Baseline susceptibility of the diamondback moth (Lepidoptera: Plutellidae) to chlorantraniliprole in China. J Econ Entomol 103:843–848

    CAS  Google Scholar 

  • Wang SL, Kang ZJ, Wu QJ, Sheng SM, Shi BC, Sheng CF (2013) Comparison of field trapping efficacy between half-shaped and whole-shaped rubber sex pheromone lure of diamondback moth [J]. China Veg 4:86–89

    CAS  Google Scholar 

  • Wang Y, Zhang Y, Wang F, Liu C, Liu K (2014) Development of transgenic Brassica napus with an optimized cry1C* gene for resistance to diamondback moth (Plutella xylostella). Can J Plant Sci 94:1501–1506

    CAS  Google Scholar 

  • Wang Y, Wei R, Zhu H, Zhou X (2015) Determination of resistance to seven insecticides in Plutella xylostella L. in fields of Northern Hunan. Agric Sci Tech 16:555–606

    Google Scholar 

  • Wei F, Wei J, Wang QL, Xu ZD, Sun Y, Yin L (2012) Study on resistance of Plutella xylostella in different areas in Hunan province to insecticides. Chin J Appl Entomol 49:477–481

    Google Scholar 

  • Wilson F (1960) A review of the biological control of insects and weeds in Australia and Australian New Guinea. Commonwealth Institute of Biological Control

  • Winkler K, Wäckers FL, Stingli A, Van Lenteren JC (2005) Plutella xylostella (diamondback moth) and its parasitoid Diadegma semiclausum show different gustatory and longevity responses to a range of nectar and honeydew sugars. Entomol Experim Applic 115:187–192

    CAS  Google Scholar 

  • Wu Q, Zhang W, Zhang Y, Xu B, Zhu G (2002) Cuticular penetration and desensitivity of GABA_ (A) receptor in abamectin resistant Plutella xylostella L. Acta Entomol Sin 45:336–340

    CAS  Google Scholar 

  • Xia F, Huanyu C, Lihua L (2001) A study on the resistance of diamondback moth to abamectin in Guangdong province. J South China Agric Uni

  • Xia Y, Lu Y, Shen J, Gao X, Qiu H, Li J (2014) Resistance monitoring for eight insecticides in Plutella xylostella in central China. Crop Prot 63:131–137

    CAS  Google Scholar 

  • Yan H-H, Xue C-B, Li G-Y, Zhao X-L, Che X-Z, Wang L-L (2014) Flubendiamide resistance and Bi-PASA detection of ryanodine receptor G4946E mutation in the diamondback moth (Plutella xylostella L.) Pestic BiochemPhysiol 115:73–77

    CAS  Google Scholar 

  • Yang HX, Wang H, Dong H, Cong B (2011) Resistance of Plutella xylostella L. to five pesticides in Shenyang. Chinese J North Hort 8:166–168

    Google Scholar 

  • Yang J et al (2015) Insight into the migration routes of Plutella xylostella in China using mt COI and ISSR markers. PLoS One 10:e0130905

    Google Scholar 

  • Yi D, Cui S, Yang L, Fang Z, Liu Y, Zhuang M, Zhang Y (2015) Influences of Cry1Ac broccoli on larval survival and oviposition of diamondback moth. J Ins Sci 15:30

    Google Scholar 

  • Yin YQ, Zhao XQ, Li XY, Chen AD (2011) The relationship between susceptibility of Plutella xylostella to insecticides and resistance. Chin J Appl Entomol 48:296–300

    CAS  Google Scholar 

  • Ying S-L (1986) A decade of successfull control of pine caterpillar, Dendrolimus punctatus Walker (lepidoptera: Lasiocampidae), by microbial agents. Forest Ecol Manag 15:69–74

    Google Scholar 

  • Zalucki M, Furlong M (2011) Predicting outbreaks of a migratory pest: an analysis of DBM distribution and abundance revisited. In: International Workshop on Management of the Diamondback Moth and Other Crucifer Insect Pests (6th, 2011). AVRDC: The World Vegetable Centre. pp 8–14

  • Zalucki MP, Shabbir A, Silva R, Adamson D, Shu-Sheng L, Furlong MJ (2012) Estimating the economic cost of one of the world’s major insect pests, Plutella xylostella (Lepidoptera: Plutellidae): just how long is a piece of string? J Econ Entomol 105:1115–1129

    Google Scholar 

  • Zhang X, He J, Ye C, Xue Y (2000) Monitoring on the resistance of diamond back moth to abamectin and field control experiments in Yunnan. J Huazhong Agric Uni 20:426–430

    Google Scholar 

  • Zhou L, Huang J, Xu H (2011) Monitoring resistance of field populations of diamondback moth Plutella xylostella L.(Lepidoptera: Yponomeutidae) to five insecticides in South China: a ten-year case study. Crop Prot 30:272–278

    CAS  Google Scholar 

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Shakeel, M., Farooq, M., Nasim, W. et al. Environment polluting conventional chemical control compared to an environmentally friendly IPM approach for control of diamondback moth, Plutella xylostella (L.), in China: a review. Environ Sci Pollut Res 24, 14537–14550 (2017). https://doi.org/10.1007/s11356-017-8996-3

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