Insect Control: Biological and Synthetic Agents - Index of

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J T Andaloro E. I. Du Pont de Nemours and Co., Newark, DE, USA P W Atkinson University of California, Riverside, CA, USA C Berry Cardiff University Park Place, Wales, UK A Bravo Universidad Nacional Autońoma de Me´xico, Cuernavaca Morelos, Mexico J-F Charles Institut Pasteur, Paris, France P Daborn University of Bath, Bath, UK I Darboux INRA, Sophia Antipolis, France T S Dhadialla Dow AgroSciences LLC, Indianapolis, IN, USA A J Dowling University of Exeter in Cornwall, Tremough Campus, Penryn, UK J E Dripps Dow AgroSciences, Indianapolis, IN, USA J Eilenberg University of Copenhagen, Frederiksberg, Denmark R H ffrench-Constant University of Exeter in Cornwall, Tremough Campus, Penryn, UK M H N L Silva Filha Centro de Pesquisas Aggeu Magalha˜es-Fundaç ão Oswaldo Cruz, Recife-PE, Brazil CONTRIBUTORS S S Gill University of California, Riverside, USA T R Glare Lincoln University, Lincoln, Christchurch, New Zealand M S Goettel Agriculture & Agri-Food Canada, Lethbridge, Canada B D Hammock University of California, Davis, USA A B Inceoglu University of California, Davis, USA P Jeschke Bayer CropScience AG, Monheim am Rhein, Germany P J Jewess Rothamsted Research, Harpenden, Hertfordshire, UK S G Kamita University of California, Davis, USA B P S Khambay Rothamsted Research, Harpenden, Hertfordshire, UK K-D Kang University of California, Davis, USA S F McCann E. I. Du Pont de Nemours and Co., Newark, DE, USA A J Mordue (Luntz) University of Aberdeen, Aberdeen, UK E D Morgan Keele University, Keele, UK
x Contributors R Nauen Bayer CropScience AG, Monheim am Rhein, Germany C Nielsen-Leroux Institut Pasteur, Paris, France A J Nisbet University of Melbourne, Werribee, Australia D A O’Brochta University of Maryland, College Park, MD, USA D Pauron INRA, Sophia Antipolis, France H Ranson Liverpool School of Tropical Medicine, Liverpool, UK A Retnakaran Canadian Forest Service, Sault Ste. Marie, ON, Canada A S Robinson FAO/IAEA Agriculture and Biotechnology Laboratory, Seibersdorf, Austria V L Salgado BASF Corporation, Research Triangle Park, NC, USA G Smagghe Ghent University, Ghent, Belgium M Soberón Universidad Nacional Autońoma de Me´xico. Cuernavaca Morelos, Mexico T C Sparks Dow AgroSciences, Indianapolis, IN, USA J Vontas University of Crete, Greece N Waterfield University of Bath, Bath, UK G B Watson Dow AgroSciences, Indianapolis, IN, USA P A Wilkinson University of Exeter in Cornwall, Tremough Campus, Penryn, UK M S Williamson Rothamsted Research, Harpenden, UK K D Wing E. I. Du Pont de Nemours and Co., Newark, DE, USA
Page 2 and 3: INSECT CONTROL BIOLOGICAL AND SYNTH
Page 4 and 5: INSECT CONTROL BIOLOGICAL AND SYNTH
Page 6 and 7: CONTENTS Preface vii Contributors i
Page 8 and 9: PREFACE When Elsevier published the
Page 12 and 13: 1 Pyrethroids B P S Khambay and P J
Page 14 and 15: activity. In contrast to most other
Page 16 and 17: Figure 1 Commercial and novel pyret
Page 18 and 19: Figure 2 Pyrethroids referred to in
Page 20 and 21: 4-position result in almost complet
Page 22 and 23: and their primary site of action is
Page 24 and 25: Figure 4 Folded and extended confor
Page 26 and 27: aromatic rings or methyl groups by
Page 28 and 29: pyrethroids) and consequently a sec
Page 30 and 31: 1998), although the precise mechani
Page 32 and 33: polymorphisms in the protein. Of th
Page 34 and 35: observed resistance to pyrethroids,
Page 36 and 37: propoxur against Culex quinquefasci
Page 38 and 39: esistance in house fly. Insect Bioc
Page 40 and 41: Shan, G.M., Hammock, B.D., 2001. De
Page 42 and 43: A1.4. Resistance The increasing num
Page 44 and 45: B A IIS4-S5 linker, IIS5 helix and
Page 46 and 47: 2 Indoxacarb and the Sodium Channel
Page 48 and 49: Figure 2 Structures of pyrazoline-l
Page 50 and 51: observed that both indoxacarb and i
Page 52 and 53: deflections resulting from stresses
Page 54 and 55: Figure 8 Dihydropyrazole block appe
Page 56 and 57: potential conduction in the CNS of
Page 58 and 59: known to affect blocker affinity, w
Page 60 and 61:
Figure 13 Diagrammatic representati
Page 62 and 63:
that the probable mechanism of ovil
Page 64 and 65:
conventional chemistries and spinos
Page 66 and 67:
Clare, J.J., Tate, S.N., Nobbs, M.,
Page 68 and 69:
Tsurubuchi, Y., Karasawa, A., Nagat
Page 70 and 71:
R1 N N O N H indoxacarb. Thus, whil
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3 Neonicotinoid Insecticides P Jesc
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esidues, like the pyrid-3-ylmethyl
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containing neonicotinoids, and neon
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Studies were also done using compar
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Becke, 1988; Klamt, 1995) level of
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sampling using forcefield methods (
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Figure 9 Stable conformations and p
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Figure 13 Binding to putative catio
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Figure 14 Systemicity of neonicotin
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site (Kayser et al., 2002). Clothia
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Figure 20 Important pest insects ta
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Barley yellow dwarf virus vectors s
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investigate the mode of action of n
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within the desensitized state over
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the accumulation of this acid in th
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3.8.1. Safety Profile The introduct
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Table 7 Environmental profile of co
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substance is bound irreversibly to
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imidacloprid conferring a high leve
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nAChR are comparable to the efficac
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Figure 25 Flea control achieved wit
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and the resolution of FAD was teste
Page 116 and 117:
Brown, J.K., Perring, T.M., Cooper,
Page 118 and 119:
In: Ishaaya, I. (Ed.), Biochemical
Page 120 and 121:
Léna, C., Changeux, J.-P., 1993. A
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patterns in Colorado potato beetle
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nach Saatgutbeizung. Pflanzenschutz
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Today, photoaffinity labeling (e.g.
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for control of stinkbugs in soybean
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Biochem. Physiol., doi: 10.1016/j.p
Page 132 and 133:
4 Insect Growth- and Development-Di
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The molting process is initiated by
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Table 1 Bisacylhydrazine insecticid
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4.2.2. Bisacylhydrazines as Tools o
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to the three EcRs with either muris
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of action of ecdysone agonists was
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thus inducing effects and symptomol
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and microsomes. Subsequently, Willi
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dipteran insects, like the midge, C
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eetle (Exomala orientalis) when app
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metabolic fate studies showed the i
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y specific proteins in signaling pa
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their reduced risk for the environm
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can be reversed by applying JH. JH
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door for a more rational approach t
Page 162 and 163:
apparent that it was a bHLH-PAS and
Page 164 and 165:
Table 9 Continued Bemisia tabaci (s
Page 166 and 167:
Table 11 Insect control with some a
Page 168 and 169:
Table 13 Ecotoxicological profile o
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Flucycloxuron Nonsystemic acaricide
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The discovery of diflubenzuron spaw
Page 174 and 175:
Table 15 Environmental effects of s
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ecessive (R male S female) manner,
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esistance management programs due t
Page 180 and 181:
IPS Paraconfusus lanier (Coleoptera
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larvae parasitized by Microplitis r
Page 184 and 185:
Kostyukovsky, M., Chen, B., Atsmi,
Page 186 and 187:
Three-dimensional quantitative stru
Page 188 and 189:
Riddiford, L.M., 1994. Cellular and
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characterization of resistant clone
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Biological Approaches to Pest Contr
Page 194 and 195:
M389 L308 M272 T304 T393 V404 L420
Page 196 and 197:
5 Azadirachtin, a Natural Product i
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and Hemiptera and was related to ef
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eported, but this is rather nonspec
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important source of pest control at
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effects with physiological effects
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eing associated with an accumulatio
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et al., 1992). Salehzadeh et al. (2
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ehavior of Spodoptera littoralis (p
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indica A. Juss. IBH Publishing Comp
Page 214 and 215:
Smith, S.L., Mitchell, M.J., 1988.
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which interact directly with azadir
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6 The Spinosyns: Chemistry, Biochem
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Table 1 Structures of the spinosyns
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Table 2 Biological activity of spin
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A large synthetic effort has gone i
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216 6: The Spinosyns: Chemistry, Bi
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Figure 4 Spinosad metabolism in avi
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A6 Addendum: The Spinosyns T C Spar
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246 A6: Addendum Scott, 2008) and i
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248 7: Bacillus thuringiensis: Mech
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A7 Addendum: Bacillus thuringiensis
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280 A7: Addendum toxins is magnitud
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Table 1 Comparative properties of s
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286 8: Mosquitocidal B. sphaericus:
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Table 4 Characteristics of various
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A8 Addendum: Bacillus sphaericus Ta
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310 A8: Addendum essential to devel
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314 9: Insecticidal Toxins from Pho
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A9 Addendum: Recent Advances in Pho
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330 A9: Addendum Lee, S.C., Stoilov
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332 10: Genetically Modified Baculo
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384 A10: Addendum cysteine protease
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388 11: Entomopathogenic Fungi and
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Zare, R., Gams, W., Culham, A., 200
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434 A11: Addendum although a number
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436 A11: Addendum Examination of ge
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440 12: Insect Transformation for U
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448 A12: Addendum genetic transform
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452 Subject Index Aphis gossypii (c
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454 Subject Index Bisacylhydrazine
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456 Subject Index Cry toxins (conti
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458 Subject Index Entomopathogenic
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460 Subject Index Homoptera molting
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462 Subject Index Kinoprene (ENSTAR
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464 Subject Index Muscle(s) sodium
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466 Subject Index Photorhabdus (con
Page 479 and 480:
468 Subject Index Sodium channel bl
Page 481:
470 Subject Index Toxocara cati, im
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