Potentiation of warfarin toxicity to roof rats (Rattus rattus) by L-histidine and by vitamin K adsorbers

The efficacy of warfarin alone or with various additives was tested against roof rats (Rattus rattus). Warfarin alone at 50 mg kg^?1 of bait killed 37% of the roof rats where-as the additives, L -histidine (40 mg kg^?1 of bait), activated-clay, charcoal and carbon (10 g kg^?1 of bait), tested individually, produced no mortality. However, when warfarin wascombined with each of these additives in turn, only the L -histidine combination resulted in 100% mortality while the other combinations killed 88, 75 and 63% of the test rats respectively. Further trials of paired comparison tests were carried out in order to evaluate the efficacy of the warfarin/L -histidine combination under different environmental conditions. All the rats succumbed to this combination in both cage and rattery conditions when there was no alternative food. Mortality decreased to 60% in cage and 70% in rattery when alternative food was provided alongside the poison bait. Rats tended to die more quickly with the L -histidine combination than with warfarin alone. Field trials also confirmed that this combination was effective in reducing roof rat infestations as shown by the yield of corpses, the post-poison bait intake and post-operational surveillance.     

Revised methodology for a blood-clotting response test for identification of warfarin-resistant Norway rats (Rattus norvegicus)

A blood-clotting response test for warfarin resistance in Norway rats ( Rattus norvegicus ) was developed by our laboratory in the late 1970s, based on knowledge of biochemical mechanisms available at that time. That test used warfarin, its the free base which is not watersoluble, and vitamin K₁ 2,3-epoxide as an antidote for warfarin-resistant rats only. We have modified the above test to use a water-soluble salt of vitamin K₃ (1 mg kgg⁻¹ body weight), which is an antidote in a wider range of warfarin-resistant rat strains than vitamin K₁ 2,3- epoxide, and a water-soluble salt of warfarin (5.4 mg kg⁻¹ body weight). Sodium warfarin and vitamin K₃ are administered by oral gavage, and the blood-clotting response measured 24 h later. In a series of validation tests there were no significant differences between results obtained by either method. The new method, however, uses materials which are commercially available, and eliminates the possibility of misclassifying warfarin-resistant rats as susceptible because vitamin K₁ 2,3-epoxide was not an antidote in those strains. We also present evidence that measuring blood-clotting response to feeding on a vitamin K-free diet for 4 days is not a reliable method for determining the genotype of warfarin-resistant rats.     

Resistance tests and field trials with bromadiolone for the control of Norway rats (Rattus norvegicus) on farms in Westphalia, Germany

BACKGROUND: The aim of this study was to determine the incidence and the level of resistance to bromadiolone among rats on farms suspected of being foci of resistance by using the international normalised ratio (INR)‐based blood clotting response (BCR) test. Whether the level of reduced susceptibility constitutes ‘practical resistance’ was subsequently determined in field trials. RESULTS: The 2.5 multiple of the ED₅₀ baseline was used to test for the incidence of resistance, and higher multiples in the range of the suspected resistance factor were used to investigate the degree of resistance. The ED₅₀ values of bromadiolone in resistant rats were confirmed in the range 4.70–7.05 mg kg^?1 for males and 4.62–6.61 mg kg^?1 for females. Variations within these ranges appeared between farms. According to the BCR resistance tests, 50–100% of rats were classified as resistant prior to the field trials; 29–100% of rats survived the treatments. CONCLUSION: BCR tests based on the use of the INR and baselines are suitable for determining the incidence and for assessing the level of resistance in populations of Norway rats. The majority of rats of the Westphalian resistant strain, characterised by the Y139C marker in VKOR, are resistant to bromadiolone under practical control conditions. Copyright © 2011 Society of Chemical Industry     

Brodifacoum is effective against Norway rats (Rattus norvegicus) in a tyrosine139cysteine focus of anticoagulant resistance in Westphalia,Germany

BACKGROUND: The tyrosine to cysteine amino acid substitution at location 139 of the vkorc1 protein (i.e. tyrosine139cysteine or Y139C) is the most widespread anticoagulant resistance mutation in Norway rats (Rattus norvegicus Berk.) in Europe. Field trials were conducted to determine the incidence of the Y139C mutation at two rat‐infested farms in Westphalia, Germany, and to estimate the practical efficacy against them of applications, using a pulsed baiting treatment regime, of a proprietary bait (Klerat^?) containing 0.005% brodifacoum. RESULTS: DNA analysis for the Y139C mutation showed that resistant rats were prevalent at the two farms, with an incidence of 80.0 and 78.6% respectively. Applications of brodifacoum bait achieved results of 99.2 and 100.0% control at the two farms, when measured by census baiting, although the treatment was somewhat prolonged at one site, possibly owing to the abundance of attractive alternative food. CONCLUSION: The study showed that 0.005% brodifacoum bait is fully effective against Norway rats possessing the Y139C mutation at the Münsterland focus and is likely to be so elsewhere in Europe where this mutation is found. The pulsed baiting regime reduced to relatively low levels the quantity of bait required to control these two substantial resistant Norway rat infestations. Previous studies had shown much larger quantities of bromadiolone and difenacoum baits used in largely ineffective treatments against Y139C resistant rats in the Münsterland. These results should be considered when making decisions about the use of anticoagulants against resistant Norway rats and their potential environmental impacts. Copyright © 2012 Society of Chemical Industry     

Rodenticide grain bait ingredient acceptance by Norway rats (Rattus norvegicus), California ground squirrels (Spermophilus beecheyi) and pocket gophers (Thomomys bottae)

Vertebrate pest control in California is often accomplished through the use of rodenticide grain baits. These grain baits are composed of steam-rolled oats (SRO), a toxicant, an indicator dye and an oil combination. A series of tests were performed to determine the effects of various dye and oil formulations on acceptance of grain bait by Norway rats [Rattus norvegicus (Berk)], California ground squirrels [Spermophilus beecheyi (Richardson)] and pocket gophers (Thomomys bottae Eyd & Gerv). Seven different dyes, four oil formulations and clean (untreated) oats were tested for acceptance. The addition of the selected oils and dyes to grain resulted in no significant differences in consumption. This indicates that there is a wide variety of dyes that could be used in the formulation of rodenticides. These alternatives could aid in proper pesticide use, the deterrence of bait consumption by birds and possibly in ingredient adhesion to the finished bait.     

Resistance testing and the effectiveness of difenacoum against Norway rats (Rattus norvegicus) in a tyrosine139cysteine focus of anticoagulant resistance,Westphalia, Germany

BACKGROUND: Anticoagulant resistance in Norway rats at foci in Belgium, Denmark, France, Germany, the Netherlands and the United Kingdom is genetically characterised by the same single nucleotide polymorphism (SNP) and consequent amino acid exchange from tyrosine to cysteine at location 139 of the vkorc1 gene (i.e. tyrosine139cysteine or Y139C). The purpose of this study was to assess the degree of resistance among rats at two infested farm sites in the Y139C focus in Westphalia, Germany, using blood clotting response (BCR) tests, and to determine the practical efficacy of applications of a commercial 50 ppm difenacoum bait (Neokil^?) against them. RESULTS: BCR tests showed that the difenacoum resistance factor (RF) among the Y139C rats was about 2.5. DNA analysis for the Y139C mutation revealed that it was present among rats at the two sites with a prevalence of 75 and 93%. Applications of difenacoum bait at the two sites achieved 86.8 and 59.9% control. The different outcomes did not appear to be due to differences either in the degree and prevalence of resistance or in the quantities of poisoned bait consumed. CONCLUSION: The study showed that, although the RF for difenacoum among rats carrying the Y139C SNP was apparently low, an acceptable level of control of resistant Norway rat infestations was not achieved using difenacoum. Continued use of anticoagulants against rats that are resistant to them will exacerbate resistance problems in terms of both increased severity and prevalence. These conclusions are likely to apply elsewhere in Europe where the Y139C SNP occurs. Copyright © 2012 Society of Chemical Industry     

Fenitrothion plus (1R)-phenothrin,and pirimiphos-methyl plus carbaryl,as grain protectant combinations for wheat

Duplicate field trials were carried out on bulk wheat in commercial silos in Queensland and New South Wales. Laboratory bioassays on samples of treated grain at intervals over 9 months, using malathion-resistant strains of insects, established that treatments were generally effective. Fenitrothion (12 mg kg^?1)+ (1R)-phenothrin (2 mg kg^?1) was more effective than pirimiphos-methyl (6 mg kg^?1) + carbaryl (10 mg kg^?1) against Sitophilus oryzae (L.) and Ephestia cautella (Walker); the order of effectiveness was reversed for S. granarius (L.). Against Rhyzopertha dominica (F.), Tribolium castaneum (Herbst), T. confusum Jackquelin du Val and Oryzaephilus surinamensis (L.), both treatments effectively prevented the production of progeny. The order of persistence was pirimiphos-methyl> (1R)-phenothrin>carbaryl or fenitrothion. During processing from wheat to white bread, residues were reduced by 98% for carbaryl, >44% for (1R)-phenothrin, 98% for fenitrothion and 85% for pirimiphosmethyl.     

不同杀虫剂及其组合对梨小食心虫初孵幼虫的毒力及田间防效

采用浸泡幼果法测定了6种杀虫剂及其两元复配组合对梨小食心虫初孵幼虫的毒力, 并将筛选出的增效组合在田间进行防效验证。结果表明, 阿维菌素、氯虫苯甲酰胺、高效氯氟氰菊酯、呋虫胺、噻虫嗪和溴氰虫酰胺对梨小食心虫初孵幼虫的致死中浓度(LC50)分别为：0.691、4.883、5.350、10.326、13.966和27.942 mg/L。两元复配组合中, 阿维菌素与呋虫胺复配组合(8∶1、2∶1、1∶1、1∶2和1∶4)、呋虫胺与氯虫苯甲酰胺复配组合(1∶4、1∶2、1∶1、2∶1和4∶1)、阿维菌素与氯虫苯甲酰胺复配组合(4∶1、1∶1和1∶4)和高效氯氟氰菊酯与呋虫胺复配组合(1∶4)具有增效作用。在梨小食心虫暴发为害年份、于梨果不同发育阶段进行田间防效验证, 阿维菌素与呋虫胺1∶4（12.5 mg/kg+50 mg/kg）、呋虫胺与氯虫苯甲酰胺2∶1(25 mg/kg+12.5 mg/kg)和阿维菌素与氯虫苯甲酰胺1∶1(12.5 mg/kg+12.5 mg/kg)对梨小食心虫的防效分别为75.02%~94.81%、50.04%~89.15%和42.90%~90.57%, 其中, 阿维菌素与呋虫胺(1∶4)的防治效果最好。     

Responses of Corcyra cephalonica (Stainton) to pirimiphos-methyl, spinosad, and combinations of pirimiphos-methyl and synergized pyrethrins

Field control failures with pirimiphos-methyl against the rice moth, Corcyra cephalonica (Stainton), in Weslaco, Texas, USA, led us to investigate the susceptibility of this particular strain to pirimiphos-methyl, spinosad, pyrethrins synergized with piperonyl butoxide, and pirimiphos-methyl combined with synergized pyrethrins. In laboratory bioassays, 50 eggs of C cephalonica were exposed to untreated and insecticide-treated corn and sunflower seeds to determine larval survival after 21 days, egg-to-adult emergence after 49 days, and larval damage to seeds at both exposure periods. Pirimiphos-methyl at both 4 and 8 mg kg(-1) did not prevent larval survival or egg-to-adult emergence of C cephalonica on either corn or sunflower seeds, and seed damage was evident at both rates. The C cephalonica strain was highly susceptible to spinosad at 0.5 and 1 mg kg(-1). At both spinosad rates, reduction in larval survival, egg-to-adult emergence, and seed damage relative to the control treatment was > or = 93% on both corn and sunflower seeds. Pirimiphos-methyl and spinosad were generally more effective against C cephalonica on corn than sunflower seeds. The C cephalonica strain was completely controlled on corn treated with 1.5 mg kg(-1) of pyrethrins synergized with 15 mg kg(-1) of piperonyl butoxide. Many larvae survived and became adults on corn treated with synergized pyrethrins at < or = 0.75 mg kg(-1). Corn treated with pirimiphos-methyl at 4, 6 or 8 mg kg(-1) in combination with 0.38 to 1.5 mg kg(-1) of synergized pyrethrins reduced larval survival by > or = 95%, egg-to-adult emergence by > or = 97%, and seed damage by > or = 94%. Our results suggest that the C cephalonica strain can be controlled on corn by combining pirimiphos-methyl with synergized pyrethrins or with synergized pyrethrins at the labeled rate. Although spinosad is not currently labeled for use on stored corn and sunflower seeds, it appears to be effective against C cephalonica on both commodities at very low rates.     

Early timing and new combinations to increase the efficacy of neonicotinoid-entomopathogenic nematode (Rhabditida: Heterorhabditidae) combinations against white grubs (Coleoptera: Scarabaeidae)

BACKGROUND: An investigation was carried out to determine whether new neonicotinoid-nematode combinations and earlier applications against younger larval stages could increase the efficacy of synergistic neonicotinoid-entomopathogenic nematode combinations against white grubs. RESULTS: In the laboratory, combinations of the neonicotinoids imidacloprid and clothianidin and the nematodes Heterorhabditis bacteriophora Poinar and H. zealandica Poinar against third instars were compared. In Anomala orientalis (Waterhouse) and Popillia japonica Newman, H. bacteriophora-imidacloprid combinations showed the most consistent synergism but did not cause significantly higher mortality than H. zealandica-imidacloprid combinations. In Cyclocephala borealis Arrow, there was no clear trend as to which combinations caused the most consistent synergism, but H. zealandica-imidacloprid combinations tended to cause the highest mortalities. In the laboratory, imidacloprid-H. bacteriophora combinations provided more consistent synergism against third-instar than against second-instar A. orientalis, but mortality was higher in second instars. In field experiments, imidacloprid-H. bacteriophora combinations against A. orientalis and P. japonica provided more consistent synergism when applied in mid-September but more consistent control when applied in late August. CONCLUSIONS: Imidacloprid is a better synergist for entomopathogenic nematodes than clothianidin. Imidacloprid-nematode combinations are more effective against second instars than against third instars, allowing rate reductions of both agents to make this approach more competitive with full-rate applications of neonicotinoid alone.     

Comparative repellent activity of single,binary and ternary combinations of plant essential oils and their major components against Sitophilus oryzae L. (Coleoptera: Curculionidae)

Journal of Plant Diseases and Protection - In the present study, repellent activity of three plant essential oils (EOs) [anise (Pimpinella anisum&nbsp;L.), eucalyptus (Eucalyptus camaldulensis...     

Enantioselective catalysis for agrochemicals: synthetic routes to (S)-metolachlor, (R)-metalaxyl and (αS,3R)-clozylacon

The application of enantioselective catalytic methods for the technical preparation of chiral agrochemicals is illustrated for three active ingredients of the acylanilide type. The key step for the technical synthesis of the herbicide (S)-metolachlor is the enantioselective hydrogenation of an imine intermediate using a novel iridium ferrocenyldiphosphine catalyst with an unprecedented high activity and 80% ee. (R)-metalaxyl and (αS,3R)-clozylacon were synthesized via the enantioselective hydrogenation of corre-sponding enamide precursors with Rh and Ru/binap catalysts with >95% and 99% enantiomeric purity, respectively. © 1998 Society of Chemical Industry     

PM 7/21 (2) Ralstonia solanacearum,R. pseudosolanacearum and R. syzygii (Ralstonia solanacearum species complex)

Specific scope

This Standard describes a diagnostic protocol for Ralstonia solanacearum, Ralstonia pseudosolanacearum and Ralstonia syzygii, i.e. phylotype/sequevar strain in the Ralstonia solanacearum Species Complex (RSSC). 1 It should be used in conjunction with PM 7/76 Use of EPPO diagnostic protocols.

Specific approval and amendment

Approved in 2003‐09. First revised in 2018‐02.     

7种农药对斜纹夜蛾的毒力测定

为了筛选出对斜纹夜蛾防效较好的农药,采用点滴法和浸叶法测定了甲维盐等7种农药对斜纹夜蛾的室内毒力.结果表明,点滴法处理后48h甲维盐的LD50为1.82μg/g,虫螨腈的LD50为2.50μg/g,高效氯氰菊酯的LD50为15.10μg/g;浸叶法处理后48h甲维盐的LC50为0.239 1mg/L,溴虫腈的LC50为0.823 2mg/L,高效氯氰菊酯的LC50为77.338 3mg/L.由此可见.甲维盐和虫螨腈对斜纹夜蛾的毒力相对较高.     

杀螨剂对朱砂叶螨的毒力测定和对加州新小绥螨的安全性评价

为评价杀螨剂对朱砂叶螨的毒力和对加州新小绥螨的安全性,本文采用玻片浸渍法、叶片残毒法和浸叶法测定了乙唑螨腈、丁氟螨酯、乙螨唑、哒螨灵、螺螨酯和联苯肼酯对朱砂叶螨的毒力,并对这6种杀螨剂对加州新小绥螨卵孵化率和雌成螨存活率进行了测定。结果表明,6种杀螨剂用叶片残毒法测定的毒力大于玻片浸渍法测定的毒力。朱砂叶螨雌成螨对螺螨酯和乙螨唑不敏感,其余4种杀螨剂都表现出较高的毒性。哒螨灵田间使用剂量显著降低加州新小绥螨雌成螨存活率,10倍田间使用剂量处理24 h后死亡率达100%。乙螨唑和哒螨灵田间使用剂量处理后加州新小绥螨卵仅有1%和0.33%的孵化率。因此,建议应用加州新小绥螨防治害螨时,应尽量避免哒螨灵和乙螨唑的施用。     

Toxicity of biorational insecticides to Helicoverpa spp. (Lepidoptera: Noctuidae) and predators in cotton field

Field trials on upland cotton (Gossypium hirstum L.) during its reproductive phase were used to assess the toxicity of several biorational pesticides and chemicals to Helicoverpa armigera (Hübner) and H. puntigera Wallengren, as well as major predators at Dalby, Queensland, Australia. Moderate rate-dependent control was obtained in plots treated with neem (Azadirachta indica A. Juss) seed extract-azadirachtin (Aza) at rates of 30, 60 and 90 g/ha. Plots treated with Talstar EC (bifenthrin) applications achieved the best results, followed by treatment with alternation of chemicals (methomyl, bifenthrin, thiodicarb and endosulfan) and biorational insecticides (neem oil, azadirachtin and Bacillus thuringiensis kurstaki var. Berliner). Predators, including lady beetles, lacewings, spiders and predatory bugs, were insensitive to Aza, tooseendanin (Tsdn) andBT applications. In contrast, chemicals were very destructive of predators. All treatments provided some protection from infestation of H. armigera and H. puntigera. The effect of Aza on Helicoverpa spp. was reflected in a relatively higher yield of seed cotton harvested from Aza-treated plots compared with the control, but chemical control achieved significantly higher yields than any other treatment.     

4种杀菌剂及其复配剂对番茄灰霉病菌的毒力

采用菌丝生长速率法测定了咯菌腈、氟啶胺、啶酰菌胺和苯醚甲环唑4种杀菌剂及其两元复配剂对番茄灰霉病菌的毒力。结果显示,咯菌腈、氟啶胺、啶酰菌胺和苯醚甲环唑对番茄灰霉病菌的有效抑制中浓度(EC50)分别为:0.018 0、0.018 1、1.896 8和2.087 4μg/mL。复配剂啶酰菌胺∶苯醚甲环唑1∶5、1∶3和1∶1,咯菌腈∶苯醚甲环唑1∶5增效作用最明显;复配剂咯菌腈∶苯醚甲环唑1∶3,咯菌腈∶氟啶胺1∶3,啶酰菌胺∶咯菌腈5∶1,啶酰菌胺∶苯醚甲环唑3∶1具有增效作用,SR值范围为1.5~4.05,其中以复配剂啶酰菌胺∶苯醚甲环唑1∶5增效作用最好,其SR值为4.05;其余不同配比的各组合复配剂具有相加作用,其SR值范围为0.5~1.46。表明咯菌腈、氟啶胺、啶酰菌胺和苯醚甲环唑4种不同作用机制的杀菌剂可以交替或复配使用,以阻止或延缓灰霉病菌抗药性的进一步加剧,为灰霉病的综合防控和抗药性治理提供理论依据。     

Toxicity of synthetic piperonyl compounds to leaf-cutting ants and their symbiotic fungus

The development of Leucoagaricus gongylophorus, the fungus cultured by the leaf-cutting ant Atta sexdens was inhibited in vitro by synthetic compounds containing the piperonyl group. In addition, worker ants that were fed daily on an artificial diet to which these compounds were added had a higher mortality rate than the controls. The inhibition of the fungal growth increased with the size of the carbon side chain ranging from C1 through C8 and decreasing thereafter. 1-(3,4-Methylenedioxybenzyloxy)octane (compound 5) was the most active compound and inhibited the fungal development by 80% at a concentration of 15 micrograms ml-1. With worker ants the toxic effects started with compound 5 and increased with the number of carbons in the side chain. Thus, for the same concentration (100 micrograms ml-1) the mortality rates observed after 8 days of diet ingestion were 82%, 66% and 42%, for 1-(3,4-methylenedioxybenzyloxy)decane, 1-(3,4-methylenedioxybenzyloxy)dodecane and compound 5, respectively, whereas with commercial piperonyl butoxide the mortality was 68%. The latter compound, which is known as a synergist insecticide, was as inhibitory to the symbiotic fungus as the synthetic compound 5. The possibility of controlling these insects in the future using compounds that can target simultaneously both organisms is discussed.