
Frederick M. Fishel2
This guide explains the rationale behind the Insecticide Resistance Action Committee's (IRAC) insecticide and acaricide mode of action classification and provides a listing of those insecticide common names with their groupings and primary modes of action for insecticides currently registered in Florida.
IRAC has groups formed in several countries, including the United States, Brazil, South Africa, Spain, India, and Australia. The group's purpose is to communicate and educate agricultural producers and crop protection professionals by providing resistance management information. Members of an IRAC group are generally professionals who are actively engaged in the insecticide and acaricide manufacturing industry. Some university researchers also participate.
Resistance refers to an inheritable change in the sensitivity of a pest population that is reflected in the repeated failure of a product to achieve the expected level of control when used according to the label recommendation for that pest species. Resistance does not always occur, but has been documented with insecticides as early as 1914. There are many known instances today where resistance is a problem. Not only has resistance occurred with insecticides but also with other pesticides, such as fungicides, herbicides, and rodenticides. Complicating the understanding and management of resistance is the problem of knowing which type of resistance is present in a given pest population. For example, some pest populations are known to have cross-resistance. That is, they are not effectively controlled with pesticides having the same mode of action that generally targets the same site within the pest. For example, both the carbamate and organophosphate insecticides target acetylcholine esterase, although each group of insecticides is chemically different from one another. The greatest resistance concern arises when multiple-resistance is confirmed. Multiple-resistance is the situation of a pest population that is resistant to pesticides having different modes of action. It is the most difficult type of resistance to manage because the number of management options is reduced. For more information on resistance, see UF/IFAS EDIS Document ENY-624, 2011 Florida Citrus Pest Management Guide: Pesticide Resistance and Resistance Management, http://edis.ifas.ufl.edu/cg026.
IRAC's insecticide classification scheme is based on mode of action. The goal of the scheme is to provide information to applicators of acaricides and insecticides so that they can make sound decisions on selecting insecticides to prevent or manage resistance. Besides selecting products that have different modes of action, growers are also encouraged to integrate other methods into insect and mite control programs. Table 1 contains those acaricides and insecticides registered for use in Florida, though it changes constantly. They are listed according to IRAC's classification scheme by their group and subgroup codes, primary target site of action, chemical sub-group or exemplifying active ingredient, and active ingredient, based on that appearing in The Pesticide Manual, 15th edition, 2009, edited by C.D.S. Tomlin, published by The British Crop Protection Council.
IRAC is currently encouraging manufacturers of pesticides to indicate the IRAC mode of action group number and description on their product labels; some registrants are now doing so, especially with newer products. Such information would be helpful in assisting pesticide applicators in the selection of acaricides and insecticides for use in resistance management strategies. An example of the manner that IRAC is encouraging registrants to list this information is as follows:
IRAC: http://www.irac-online.org/groups/guide/
Rogers, M.E., and M. M. Dewdney. 2010. 2011 Florida citrus pest management guide: pesticide resistance and resistance management. UF/IFAS EDIS Document ENY-624. http://edis.ifas.ufl.edu/cg026.
Tomlin, C.D.S. Ed. 2009. The pesticide manual. 15th edition, The British Crop Protection Council. 1250 pp., ISBN 1 901396 13 4.
IRAC's classification scheme for acaricides and insecticides registered for use in Florida.
Group |
Subgroup |
Primary target site of action |
Chemical subgroup or exemplifying active ingredient |
Active ingredients |
1* |
1A |
Acetylcholine esterase inhibitors |
Carbamates |
Aldicarb Bendiocarb Carbaryl Carbofuran Methiocarb Methomyl Oxamyl Propoxur Thiodicarb |
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1B |
Organophosphates |
Acephate Azinphos-methyl Chlorpyrifos Chlorpyrifos-methyl Coumaphos Diazinon Dichlorvos Dicrotophos Dimethoate Disulfoton Ethion Ethoprop Fenamiphos Fenthion Fosthiazate Isofenphos Malathion Methamidophos Methidathion Methyl parathion Naled Oxydemeton-methyl Phorate Profenofos Propetamphos Temephos Terbufos Tetrachlorvinphos Trichlorfon |
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2 |
2A |
GABA-gated chloride channel antagonists |
Cyclodiene organochlorines |
Endosulfan |
2B |
Phenylpyrazoles (Fiproles) |
Fipronil |
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3* |
3A |
Sodium channel modulators |
Pyrethroids Pyrethrins |
Allethrin and isomers Bifenthrin and isomers Cyfluthrin and isomers Cyhalothrin and isomers Cypermethrin and isomers Cyphenothrin Deltamethrin Esfenvalerate Fenpropathrin Fenvalerate Imiprothrin Permethrin Phenothrin Prallethrin Pyrethrins (pyrethrum) Resmethrin Tefluthrin Tetramethrin Tralomethrin |
3B |
Methoxychlor |
Methoxychlor |
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4 |
4A |
Nicotinic acetylcholine receptor agonists |
Neonicotinoids |
Acetamiprid Clothianidin Dinotefuran Imidacloprid Thiamethoxam |
4B |
Nicotine |
Nicotine |
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5 |
Nicotinic acetylcholine receptor allosteric activators |
Spinosyns |
Spinetoram Spinosad |
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6 |
Chloride channel activators |
Avermectins, Milbemycins |
Abamectin Emamectin benzoate Milbemectin |
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7 |
7A |
Juvenile hormone mimics |
Juvenile hormone analogues |
Hydroprene |
Kinoprene |
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7B |
Fenoxycarb |
Fenoxycarb |
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7C |
Pyriproxyfen |
Pyriproxyfen |
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8 |
8A |
Miscellaneous non-specific (multi-site) inhibitors |
Alkyl halides |
Methyl bromide and other alkyl halides |
8B |
Chloropicrin |
Chloropicrin |
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8C |
Sulfuryl fluoride |
Sulfuryl fluoride |
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8D |
Borax |
Borax |
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10 |
10A |
Mite growth inhibitors |
Clofentezine Hexythiazox |
Clofentezine Hexythiazox |
10B |
Etoxazole |
Etoxazole |
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11 |
Microbial disruptors of insect midgut membranes (includes transgenic crops expressing B.t. toxins) |
Bacillus thuringiensis or Bacillus sphaericus and the insecticidal proteins they produce |
Bacillus thuringiensis subsp. israelensis Bacillus sphaericus Bacillus thuringiensis subsp. Kurstaki Bt crop proteins |
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12 |
12B |
Inhibitors of mitochondrial ATP synthase |
Organotin miticides |
Fentutatin oxide |
12C |
Propargite |
Propargite |
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13 |
Uncouplers of oxidative phosphorylation via disruption of the proton gradient |
Chlorfenapyr |
Chlorfenapyr |
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15 |
Inhibitors of chitin biosynthesis, type 0, Leptdopteran |
Benzoylureas |
Diflubenzuron Hexaflumuron Lufenuron Novaluron Noviflumuron |
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16 |
Inhibitors of chitin biosynthesis, type 1 |
Buprofezin |
Buprofezin |
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17 |
Moulting disruptor, Dipteran |
Cyromazine |
Cyromazine |
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18 |
Ecdysone receptor agonists |
Diacylhydrazines |
Halofenozide Methoxyfenozide Tebufenozide |
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19 |
Octopamine receptor agonists |
Amitraz |
Amitraz |
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20* |
20A |
Mitochondrial complex III electron transport inhibitors |
Hydramethylnon |
Hydramethylnon |
20B |
Acequinocyl |
Acequinocyl |
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21* |
21A |
METI acaricides and insecticides |
Fenazaquin |
Fenazaquin Fenpyroximate Pyridaben Tolfenpyrad |
21B |
Mitochondrial complex I electron transport inhibitors |
Rotenone |
Rotenone |
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22* |
22A |
Voltage-dependent sodium channel blockers |
Indoxacarb |
Indoxacarb |
22B |
Metaflumizone |
Metaflumizone |
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23 |
Inhibitors of acetyl CoA carboxylase |
Tetronic and tetramic acid derivatives |
Spirodiclofen Spiromesifen Spirotetramat |
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24 |
24A |
Mitochondrial complex IV electron transport inhibitors |
Phosphine | Aluminum phosphide Phosphine Zinc phosphide |
28 |
Ryanodine receptor modulators |
Diamides |
Chlorantraniliprole Flubendiamide |
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UN |
Compounds of unknown or uncertain mode of action@ |
Azadirachtin |
Azadirachtin |
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Bifenazate |
Bifenazate |
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Cryolite |
Cryolite |
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Dicofol |
Dicofol |
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Pyridalyl |
Pyridalyl |
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*Groups and Sub-groups: Although sharing the same primary target site, it is possible that not all members of a single mode of action class have been shown to be cross-resistant. Different resistance mechanisms that are not linked to the target site, such as enhanced metabolism, may be common for such a group of chemicals. In such cases, the mode of action grouping is further divided into sub-groups. @A compound with an unknown or controversial mode of action or an unknown mode of toxicity will be held in category UN until evidence becomes available to enable that compound to be assigned to a more appropriate mode of action class. |
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This document is PI-83, one of a series of the Pesticide Information Office, Florida Cooperative Extension Service, Institute of Food and Agricultural Sciences, University of Florida. Original publication date October 2005. Revised April 2011. Visit the EDIS website at http://edis.ifas.ufl.edu.
Frederick M. Fishel, associate professor, Agronomy Department, and director, Pesticide Information Office; Florida Cooperative Extension Service, Institute of Food and Agricultural Sciences, University of Florida, Gainesville, FL 32611.
The use of trade names in this publication is solely for the purpose of providing specific information. UF/IFAS does not guarantee or warranty the products named, and references to them in this publication do not signify our approval to the exclusion of other products of suitable composition. Use pesticides safely. Read and follow directions on the manufacturer's label.
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